HomeMy WebLinkAboutNC0024406_2017 Final CSA Updated_201710312017 Comprehensive Site Assessment Update October 2017
Belews Creek Steam Station SynTerra
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Explanation of altered or items not initialed:
Item 1. The CSA was specifically designed to assess the coal ash
management areas of the facility. Sufficient information is
available to prepare the groundwater corrective action plan for
the ash management areas of the facility. Data limitations are
discussed in Section 11.3 of the CSA report. Continued
groundwater monitoring at the Site is planned.
Item 2. Imminent hazards to human health and the environment have
been evaluated. The NCDEQ data associated with nearby water
supply wells is provided herein and is being evaluated.
Item 5. The groundwater assessment plan for the CSA as approved by
NCDEQ was specifically developed to assess the coal ash
management areas of the facility for the purposes of developing
a corrective action plan for groundwater. Other areas of possible
contamination on the property were not evaluated.
2017 Comprehensive Site Assessment Update October 2017
Belews Creek Steam Station SynTerra
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WORK PERFORMED BY OTHERS
• HDR Engineering, Inc. (HDR) of the Carolinas prepared the reports referenced herein under
contract to Duke Energy.
• The reports were sealed by licensed geologists or engineers as required by the North Carolina
Board for Licensing of Geologists or Board of Examiners for Engineers and Surveyors.
• The evaluations of hydrogeologic conditions and other information provided in this updated
Comprehensive Site Assessment (CSA) are based in part on the work contained in the HDR
documents and on sampling activities performed by Pace Analytical Services after the
submittal of the HDR documents. The evaluations described in this paragraph meet
requirements detailed in 15A NCAC 02L .0106(g).
• SynTerra relied on information from the HDR reports as being correct. SynTerra has proofread
boring logs; monitoring well installation records; and data tables presenting chemical,
physical, and hydraulic properties of ash, soil, rock, groundwater, and surface water, and has
made corrections where mistakes were found. SynTerra did not perform additional validation
activities concerning the HDR reports. SynTerra has found no reason to question geological
interpretations of site hydrostratigraphic information and other information in the HDR reports.
• The seal of the licensed geologist for this CSA applies to activities conducted and
interpretations derived after the HDR reports were submitted. This submittal relies on the
professional work performed by HDR and references that work.
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EXECUTIVE SUMMARY
ES.1 Source Information
Duke Energy Carolinas, LLC (Duke Energy) owns and operates the Belews Creek Steam
Station (BCSS), which is located on Belews Reservoir in Belews Creek, Stokes County,
North Carolina. The Comprehensive Site Assessment (CSA) update was conducted to
refine and expand the understanding of subsurface geologic/hydrogeologic conditions
and evaluate the extent of impacts from historical management of coal ash. This CSA
update contains an assessment of site conditions based on a comprehensive
interpretation of geologic and sampling results from the initial site assessment and
geologic and sampling results obtained subsequent to the initial assessment.
BCSS began operation in 1974 as a coal-fired generating station and currently operates
two coal-fired units. Prior to 1984, BCSS has disposed of coal combustion residuals
(CCR) from the coal combustion process in the ash basin located across Pine Hall Road
to the west-northwest of the station. The ability to sluice fly ash to the ash basin is
available but is limited to certain situations (i.e. unit startup/shutdown, equipment
maintenance and service) but is primarily disposed in permitted landfills located at the
site. The station’s ash basin consists of a single cell impounded by an earthen main dam
located on the north end of the ash basin and an embankment dam located in the
northeast portion of the basin. The ash basin main dam was constructed from 1970 to
1972 and is located approximately 3,200 feet northwest of the BCSS powerhouse.
The North Carolina Department of Environmental Quality (NCDEQ) Division of Water
Resources (DWR) currently permits discharge from the ash basin under the National
Pollutant Discharge Elimination System (NPDES) Permit NC0024406. The discharge
from the ash basin is through a concrete discharge tower located in the northwest
portion of the ash basin. The concrete discharge tower drains through a 21-inch inside
diameter high-density polyethylene (HDPE) conduit for approximately 1,600 feet and
then discharges into a concrete flume box. From the flume box the discharge is routed
through the designated effluent channel that flows northwest to the Dan River. The ash
basin originally discharged to Belews Reservoir through a concrete discharge tower
located at the northeast end of the ash basin.
Assessment results indicate the thickness of CCR in the ash basin ranges from a few feet
to approximately 66 feet. Assessment findings determined that CCR accumulated in
the ash basin is the primary source of impact to groundwater. The inferred general
extent of constituent migration in groundwater based on evaluation of concentrations
greater than both site background and groundwater quality standards is shown on
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Figure ES-1. A detailed evaluation of constituent migration is included in the CSA
update report.
ES.2 Initial Abatement and Emergency Response
Duke Energy has not conducted emergency responses because groundwater impacts
from the ash basin do not present an imminent and substantial threat to the
environment requiring emergency response.
A Settlement Agreement between NCDEQ and Duke Energy signed on September 29,
2015, requires accelerated groundwater remediation to be implemented at sites that
demonstrate off-site groundwater impacts. Assessment information indicates the
potential for off-site groundwater impact northwest of the BCSS ash basin toward an
undeveloped 2.23-acre parcel (hereafter referred to as Parcel A) not owned by Duke
Energy.
A groundwater extraction system, located between the ash basin and the southeast side
of Parcel A, is designed and will be installed to control groundwater flow from the ash
basin prior to migration toward Parcel A. The 100% Basis of Design (BOD) report was
submitted to NCDEQ on September 1, 2017.
In preparation for the ash basin closure, a dry bottom ash handling system, new
retention basins, and wastewater treatment systems are being designed and
constructed. The reduction of inflows to the basin is an initial abatement measure.
ES.3 Receptor Information
In accordance with NCDEQ direction, CSA receptor survey activities include listing and
depicting all water supply wells (public or private, including irrigation wells and
unused wells) within a 0.5-mile radius of the ash basin compliance boundary.
ES.3.1 Public Water Supply Wells
One public water supply well was identified within a 0.5-mile radius of the ash
basin compliance boundary. It is located at the Withers Chapel United
Methodist Church (UMC) located offsite approximately 1,750 feet (0.3 miles)
northeast of the BCSS ash basin, in an area hydraulically upgradient from
groundwater flow associated with the ash basin.
ES.3.2 Private Water Supply Wells
Approximately 50 private water supply wells (including irrigation wells and
unused wells) were identified within a 0.5-mile radius of the ash basin
compliance boundary. The private water supply wells are located hydraulically
upgradient or sidegradient from the ash basin.
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Private water supply wells are assumed to be open borehole bedrock wells. The
water supply well data does not reflect characteristic ash basin constituents.
Constituent concentrations in bedrock groundwater directly downgradient of the
ash basin are less than 2L with the exception of manganese, which appears to be
due to geochemical conditions. The water chemistry signature of the water
supply wells is similar to the background bedrock wells at the site. Although
several water supply well concentrations reported are greater than the site
specific provisional background threshold values (PBTVs), the concentrations are
within the background concentration range for similar Piedmont geologic
settings.
ES.3.3 Surface Water Bodies
Several surface water bodies flow from the topographic divide along Middleton
Loop Road toward the Dan River within a 0.5-mile radius of the ash basin.
Belews Reservoir is also located within the 0.5-mile receptor survey radius.
Surface water intakes include two from Belews Reservoir for BCSS plant
operations and for water trucks at the Craig Road Landfill. A backup intake is
located on the Dan River. The surface water intakes are for non-potable uses.
ES.3.4 Human and Ecological Receptors
A baseline human health and ecological risk assessment was performed in 2016
as a component of Corrective Action Plan (CAP) 2 (HDR, 2016). Water supply
well data collected since the risk assessment was completed indicates several
wells located to the west-southwest and northeast of the ash basin had
concentrations of chromium, cobalt, iron, manganese, vanadium that exceeded
their respective water quality standards, however all reported concentrations
were less than their respective EPA risk-based tap water screening levels. As
previously noted, the wells are located upgradient or a sufficient distance
sidegradient to not be impacted by groundwater migration from the ash basin.
The ecological risk assessment considered surface water data associated with
Belews Reservoir beyond the extent of constituent migration in groundwater
from the ash basin. As such, the findings for the Belews Reservoir do not imply
adverse effects associated with groundwater to surface water migration from the
ash basin. This exposure route will be further evaluated through direct surface
water sampling and predictive modeling as part of the CAP. To date, 2B and
EPA water quality criteria have not been exceeded in waters proximal to areas of
groundwater impact.
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ES.3.5 Land Use
The area surrounding BCSS generally consists of residential properties, farm
land, undeveloped land, and Belews Reservoir. Properties located within the 0.5-
mile radius of the BCSS ash basin compliance boundary generally consist of
residential properties located to the southwest and residential farm land
northeast, north, and west. Duke Energy property is located to the north,
northwest, south, and east with Belews Reservoir to the south and east. No
change in surrounding land use is currently anticipated.
ES.4 Sampling/Investigation Results
The comprehensive site assessment included evaluations of the hydrogeological and
geochemical properties of soil and groundwater at multiple depths and distances from
the ash basin.
ES.4.1 Background Concentration Determinations
Naturally occurring background concentrations, Provisional Background
Threshold Values (PBTVs), were determined using statistical analysis for both
soil and groundwater at the site. Statistical determinations of PBTVs were
performed in strict accordance with the revised Statistical Methods for Developing
Reference Background Concentrations for Groundwater and Soil at Coal Ash Facilities
(statistical methods document) (HDR and SynTerra, 2017). The background
monitoring well network consists of wells installed within three flow layers –
shallow, deep (transition zone), and fractured bedrock. Background datasets
were used to statistically determine naturally occurring concentrations of
inorganic constituents in soil and groundwater. As of September 1, 2017, DEQ
approved a number of the statistically derived background values, however
others are still under evaluation and thus considered preliminary at this
time. Background results may be greater than the PBTVs due to the limited valid
dataset currently available. The statistically derived background threshold
values will continue to be adjusted as additional data becomes available.
ES.4.2 Nature and Extent of Contamination
Site-specific groundwater constituents of interest (COIs) were developed by
evaluating groundwater sampling results with respect to 2L/IMACs and PBTVs,
and additional regulatory input/requirements. The distribution of constituents in
relation to the ash basin, co-occurrence with CCR indicator constituents such as
boron, and likely migration directions based on groundwater flow direction are
considered in determination of groundwater COIs.
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The following list of groundwater COIs has been developed for BCSS:
Antimony Iron
Arsenic Manganese
Barium Molybdenum
Beryllium pH
Boron Selenium
Cadmium Strontium
Chloride Sulfate
Chromium (hexavalent) TDS (Total Dissolved Solids)
Chromium (total) Thallium
Cobalt Vanadium
Boron is a CCR-derived constituent in groundwater and is detected at
concentrations greater than the 2L standard beneath and downgradient of the
ash basin. Boron is not detected in background groundwater. The horizontal
extent of boron concentrations greater than 2L approximates the leading edge of
the CCR-derived plume from the source areas (Figure ES-1).
Boron is detected in groundwater at concentrations greater than 2L in the
shallow flow layer primarily north of the ash basin main dam, within the
compliance boundary, and northwest of the ash basin, at or beyond the
compliance boundary. In the deep flow layer boron concentrations greater than
2L occur beneath the ash basin and the Pine Hall Road Landfill, north of the ash
basin main dam, within the compliance boundary, and northwest of the ash
basin, at or beyond the compliance boundary.
Boron concentrations greater than 2L are also reported west of the Structural Fill,
which is south of the ash basin and topographic divide along Pine Hall Road.
The boron south of Pine Hall Road appears to be related to the Structural Fill
where an assessment is ongoing. Boron concentrations less than 2L have been
reported in the bedrock flow layer with the exception of a grout contaminated
well beneath the ash basin main dam.
Beryllium, chloride, chromium, cobalt, manganese, and thallium are also
constituents detected in groundwater greater than background and 2L/IMAC
near or beyond the compliance boundary. The interpreted extent of beryllium
concentrations greater than background and the IMAC is beyond the compliance
boundary in the shallow and deep flow layers. Beryllium was not reported at a
concentration greater than the IMAC in the bedrock flow layer. The interpreted
extent of chloride concentrations greater than 2L at and beyond the compliance
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boundary is in the shallow and deep flow layers. Chloride was not reported at a
concentration greater than 2L in the bedrock flow layer. The interpreted extent of
chromium concentrations greater than 2L at and beyond the compliance
boundary is in the shallow and deep flow layers. Chromium was not reported at
a concentration greater than 2L in the bedrock flow layer. The interpreted extent
of cobalt concentrations greater than IMAC at and beyond the compliance
boundary is in the shallow flow layer only. Cobalt exceedances were not
reported in the deep and bedrock flow layers. The interpreted extent of
manganese concentrations greater than 2L at and beyond the compliance
boundary is in the shallow, deep, and bedrock flow layers. The interpreted
extent of thallium concentrations greater than the IMAC at and beyond the
compliance boundary is in the shallow and deep flow layers. Thallium was not
reported at a concentration greater than 2L in the bedrock flow layer.
The bedrock aquifer is generally the source of water for supply wells in the area.
As outlined above, the bedrock aquifer has not been impacted by CCR
constituent migration from the ash basin with the exception of a grout
contaminated well beneath the ash basin main dam. The manganese
concentrations reported in bedrock groundwater are likely due to natural
geochemical conditions.
In ash basin locations where soil samples were collected beneath the ash,
analytical results indicate arsenic and selenium concentrations greater than
PBTVs and PSRGs for POG are present. Strontium was also reported in five of
the soil samples collected beneath the ash basin at concentrations greater than the
background concentration. There is no PSRG POG for strontium. No other COIs
were detected in soil beneath the ash basin at concentrations greater than PBTVs
or PSRG POGs.
ES.4.3 Maximum Contaminant Concentrations
(Source Information)
The source areas at BCSS include CCR material in the ash basin including the
former chemical pond and the Pine Hall Road Landfill. Ash pore water samples
collected from wells installed within the ash basin and screened in the ash layer
have been monitored since 2015. The concentrations of detected constituents
have been relatively stable with minor fluctuations. The ash basins are permitted
wastewater systems; therefore comparison of pore water within the wastewater
treatment residuals (ash) to 2B or 2L/IMAC is not required.
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Soil samples collected below the ash/soil interface from locations within the ash
basins indicate arsenic, selenium, and strontium reported at concentrations
greater than their respective PSRG Protection of Groundwater (POG) and/or soil
PBTV values.
ES.4.4 Site Geology and Hydrogeology
Based on the site investigation, the groundwater system in natural materials
(soil, soil/saprolite, and bedrock) at the BCSS site is consistent with the regolith-
fractured rock system and is an unconfined, connected aquifer system. Regolith
is underlain by a transition zone (TZ) of weathered rock which transitions to
competent bedrock. The groundwater system at the BCSS site is divided into
three flow layers referred to in this report as the shallow, deep (TZ), and bedrock
layers, so as to distinguish unique characteristics of the connected aquifer
system. The shallow flow layer generally consists of surficial material such as
soil and fill. The deep flow layer includes both saprolite and weathered rock,
while the bedrock layer is competent bedrock with limited fractures.
A topographic and hydrologic divide (highest topographic portion of the Site) is
generally located along Pine Hall Road south of the ash basin. Groundwater
flow contours developed from water level elevations measured in the shallow,
deep and bedrock wells indicate groundwater flow from the ash basin is
generally to the north and northwest toward the Dan River and to the east
toward Belews Reservoir.
ES.5 Conclusions and Recommendations
The investigation described in the CSA presents the results of the assessments required
by CAMA and 2L. The ash basin was determined to be a source of the groundwater
contamination.
The BCSS ash basin is currently designated as “Intermediate” risk under CAMA,
requiring closure of the ash basin by 2024. However, groundwater and surface water
quality data provide no indications of potential risk to human and wildlife receptors
related to constituent migration through the groundwater pathway from the ash basin.
These findings support a proposed “low” risk classification.
Impacts to soil were determined to be limited to a shallow interval below the ash. Soil
samples collected from below the ash basin exhibited concentrations greater than POG
PSRGs and/or PBTVs for arsenic, selenium and strontium. Those shallow soil impacts
are anticipated to be addressed through basin closure and the CAP.
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Boron, beryllium, chloride, chromium, cobalt, manganese, and thallium are the primary
constituents detected in groundwater greater than PBTVs and 2L/IMAC near or beyond
the compliance boundary. The interpreted extent of exceedances are within the shallow
and/or deep flow layers with the exception of manganese.
The bedrock aquifer is generally the source of water for supply wells in the area. As
outlined above, the bedrock aquifer has not been impacted by CCR constituent
migration from the ash basin with the exception of a grout contaminated well beneath
the ash basin main dam. The manganese concentrations reported in bedrock
groundwater are likely due to natural geochemical conditions.
A preliminary evaluation of groundwater corrective action alternatives is included in
this CSA to provide insight into the CAP preparation process. For BCSS, the primary
source control (closure) methods anticipated to be evaluated in the CAP are:
Dewater the ash within the basin and cap the residuals with a low
permeability engineered cover system to minimize infiltration;
Excavate the ash to remove the source of the COIs from the groundwater flow
system; and
Some combination of the above.
The source control (closure) options will be evaluated in the CAP to determine the most
technically and economically feasible means of removing or controlling the ash and ash
pore water as a source to the groundwater flow system. The evaluation will include
predictive groundwater modeling to evaluate the cost-benefit associated with various
options.
For basin closure, ash dewatering and reduction of the amount of water migrating from
the basin to groundwater will have the greatest positive impact on groundwater and
surface water quality downgradient of the ash basin. A well-designed capping system
can be expected to minimize ongoing migration to groundwater after dewatering.
In addition to source control measures, the CAP will evaluate measures to address
groundwater conditions associated with the ash basin. Groundwater corrective action
by monitored natural attenuation (MNA) is anticipated to be a remedy further
evaluated in the CAP. As warranted, a number of viable groundwater remediation
technologies such as phytoremediation, groundwater extraction, or hydraulic barriers
may be evaluated based upon short-term and long-term effectiveness, feasibility, and
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cost. Results of the evaluation, including groundwater fate and transport modeling,
and geochemical modeling, will be used for remedy selection in the CAP.
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TABLE OF CONTENTS
SECTION PAGE
ES.1 SOURCE INFORMATION ....................................................................................... ES-1
ES.2 INITIAL ABATEMENT AND EMERGENCY RESPONSE ................................ ES-2
ES.3 RECEPTOR INFORMATION .................................................................................. ES-2
ES.3.1 Public Water Supply Wells ................................................................................... ES-2
ES.3.2 Private Water Supply Wells ................................................................................. ES-2
ES.3.3 Surface Water Bodies ............................................................................................. ES-3
ES.3.4 Human and Ecological Receptors ........................................................................ ES-3
ES.3.5 Land Use .................................................................................................................. ES-4
ES.4 SAMPLING/INVESTIGATION RESULTS .......................................................... ES-4
ES.4.1 Background Concentration Determinations ...................................................... ES-4
ES.4.2 Nature and Extent of Contamination .................................................................. ES-4
ES.4.3 Maximum Contaminant Concentrations (Source Information) ..................... ES-6
ES.4.4 Site Geology and Hydrogeology ......................................................................... ES-7
ES.5 CONCLUSIONS AND RECOMMENDATIONS ................................................ ES-7
1.0 INTRODUCTION ......................................................................................................... 1-1
Purpose of Comprehensive Site Assessment ........................................................ 1-1 1.1
Regulatory Background ........................................................................................... 1-2 1.2
Notice of Regulatory Requirements (NORR) ............................................... 1-2 1.2.1
Coal Ash Management Act Requirements .................................................... 1-3 1.2.2
Approach to Comprehensive Site Assessment ..................................................... 1-4 1.3
NORR Guidance ................................................................................................ 1-4 1.3.1
USEPA Monitored Natural Attenuation Tiered Approach ........................ 1-5 1.3.2
ASTM Conceptual Site Model Guidance ....................................................... 1-5 1.3.3
Technical Objectives ................................................................................................. 1-5 1.4
Previous Submittals .................................................................................................. 1-6 1.5
2.0 SITE HISTORY AND DESCRIPTION ..................................................................... 2-1
Site Description, Ownership and Use History ...................................................... 2-1 2.1
Geographic Setting, Surrounding Land Use, Surface Water Classification ..... 2-2 2.2
CAMA-related Source Areas ................................................................................... 2-4 2.3
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TABLE OF CONTENTS CONTINUED
SECTION PAGE
Other Primary and Secondary Sources .................................................................. 2-5 2.4
Summary of Permitted Activities ........................................................................... 2-6 2.5
History of Site Groundwater Monitoring .............................................................. 2-8 2.6
Ash Basin ............................................................................................................ 2-8 2.6.1
Landfill Groundwater Monitoring ................................................................. 2-9 2.6.2
Ash Basin CAMA Monitoring ....................................................................... 2-10 2.6.3
Summary of Assessment Activities ...................................................................... 2-11 2.7
Summary of Initial Abatement, Source Removal or other Corrective Action 2-13 2.8
3.0 SOURCE CHARACTERISTICS ................................................................................. 3-1
Coal Combustion and Ash Handling System ....................................................... 3-1 3.1
General Physical and Chemical Properties of Ash .............................................. 3-2 3.2
Site-Specific Coal Ash Data ..................................................................................... 3-5 3.3
4.0 RECEPTOR INFORMATION ..................................................................................... 4-1
Summary of Receptor Survey Activities................................................................ 4-2 4.1
Summary of Receptor Survey Findings ................................................................. 4-3 4.2
Public Water Supply Wells .............................................................................. 4-4 4.2.1
Private Water Supply Wells ............................................................................ 4-4 4.2.2
Private and Public Well Water Sampling .............................................................. 4-5 4.3
Numerical Well Capture Zone Analysis ............................................................... 4-8 4.4
Surface Water Receptors .......................................................................................... 4-8 4.5
5.0 REGIONAL GEOLOGY AND HYDROGEOLOGY ............................................... 5-1
Regional Geology ...................................................................................................... 5-1 5.1
Regional Hydrogeology ........................................................................................... 5-2 5.2
6.0 SITE GEOLOGY AND HYDROGEOLOGY ............................................................ 6-1
Site Geology ............................................................................................................... 6-2 6.1
Soil Classification .............................................................................................. 6-2 6.1.1
Rock Lithology .................................................................................................. 6-4 6.1.2
Structural Geology ............................................................................................ 6-4 6.1.3
Soil and Rock Mineralogy and Chemistry .................................................... 6-5 6.1.4
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TABLE OF CONTENTS CONTINUED
SECTION PAGE
Geologic Mapping ............................................................................................. 6-6 6.1.5
Effects of Geologic Structure on Groundwater Flow ................................... 6-7 6.1.6
Site Hydrogeology .................................................................................................... 6-7 6.2
Hydrostrographic Layer Development ......................................................... 6-7 6.2.1
Hydrostrographic Layer Properties ............................................................... 6-8 6.2.2
Groundwater Flow Direction .................................................................................. 6-9 6.3
Hydraulic Gradient ................................................................................................. 6-10 6.4
Hydraulic Conductivity ......................................................................................... 6-11 6.5
Groundwater Velocity ............................................................................................ 6-12 6.6
Contaminant Velocity ............................................................................................. 6-13 6.7
Slug Test and Aquifer Test Results....................................................................... 6-14 6.8
Fracture Trace Study Results (if applicable) ....................................................... 6-15 6.9
Methods ............................................................................................................ 6-15 6.9.1
Results ............................................................................................................... 6-16 6.9.2
7.0 SOIL SAMPLING RESULTS ...................................................................................... 7-1
Background Soil Data ............................................................................................... 7-1 7.1
Facility Soil Data ....................................................................................................... 7-2 7.2
8.0 SEDIMENT RESULTS ................................................................................................. 8-1
Sediment/Surface Soil Associated with AOWs .................................................... 8-1 8.1
Sediment in Major Water Bodies ............................................................................ 8-3 8.2
9.0 SURFACE WATER RESULTS .................................................................................... 9-5
Comparison of Exceedances to 2B Criteria ........................................................... 9-8 9.1
Discussion of Results for Constituents Without Established 2B ........................ 9-9 9.2
Discussion of Surface Water Results .................................................................... 9-12 9.3
10.0 GROUNDWATER SAMPLING RESULTS ............................................................ 10-1
Background Groundwater Concentrations ......................................................... 10-2 10.1
Background Dataset Statistical Analysis ..................................................... 10-4 10.1.1
Piper Diagrams (Comparison to Background) ........................................... 10-6 10.1.2
Downgradient Groundwater Concentrations ..................................................... 10-7 10.2
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TABLE OF CONTENTS CONTINUED
SECTION PAGE
Piper Diagrams (Comparison to Downgradient/ Separate Flow Regime)10-10.2.1
12
Site-Specific Exceedances (Groundwater COIs) ............................................... 10-13 10.3
Provisional Background Threshold Values (PBTVs) ............................... 10-13 10.3.1
Applicable Standards ................................................................................... 10-13 10.3.2
Additional Requirements ............................................................................. 10-14 10.3.3
BCSS Groundwater COIs ............................................................................. 10-15 10.3.4
Water Supply Well Groundwater Concentrations and Exceedances ............ 10-17 10.4
11.0 HYDROGEOLOGICAL INVESTIGATION .......................................................... 11-1
Plume Physical Characterization .......................................................................... 11-1 11.1
Plume Chemical Characterization ........................................................................ 11-4 11.2
Pending Investigations ......................................................................................... 11-25 11.3
12.0 RISK ASSESSMENT .................................................................................................. 12-1
Human Health Screening Summary .................................................................... 12-2 12.1
Ecological Screening Summary ............................................................................. 12-3 12.2
Private Well Receptor Assessment Update ......................................................... 12-3 12.3
Risk Assessment Update Summary ..................................................................... 12-5 12.4
13.0 GROUNDWATER MODELING RESULTS ........................................................... 13-1
Summary of Fate and Transport Model Results................................................. 13-2 13.1
Flow Model Construction .............................................................................. 13-3 13.1.1
Transport Model Construction ..................................................................... 13-7 13.1.2
Summary of Flow and Transport Modeling Results To Date .................. 13-9 13.1.3
Summary of Geochemical Model ....................................................................... 13-12 13.2
Model Construction ...................................................................................... 13-12 13.2.1
Summary of Geochemical Model Results To Date ................................... 13-16 13.2.2
Groundwater to Surface Water Pathway Evaluation ...................................... 13-16 13.3
14.0 SITE ASSESSMENT RESULTS ................................................................................ 14-1
Nature and Extent of Contamination ................................................................... 14-1 14.1
Maximum Constituent Concentrations ............................................................... 14-6 14.2
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TABLE OF CONTENTS CONTINUED
SECTION PAGE
Contaminant Migration and Potentially Affected Receptors ........................... 14-7 14.3
15.0 CONCLUSIONS AND RECOMMENDATIONS ................................................. 15-1
Overview of Site Conditions at Specific Source Areas ...................................... 15-1 15.1
Revised Site Conceptual Model ............................................................................ 15-2 15.2
Interim Monitoring Program ................................................................................. 15-4 15.3
IMP Implementation ....................................................................................... 15-4 15.3.1
IMP Reporting ................................................................................................. 15-5 15.3.2
Preliminary Evaluation of Corrective Action Alternatives............................... 15-5 15.4
CAP Preparation Process ............................................................................... 15-6 15.4.1
Summary .......................................................................................................... 15-8 15.4.2
16.0 REFERENCES ............................................................................................................... 16-1
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LIST OF FIGURES
Executive Summary
Figure ES-1 Approximate Extent of Impacts
1.0 Introduction
Figure 1-1 Site Location Map
2.0 Site History and Description
Figure 2-1 Site Layout Map
Figure 2-2 1951 Aerial Photograph
Figure 2-3 1966 Aerial Photograph
Figure 2-4 1971 Aerial Photograph
Figure 2-5 1977 Aerial Photograph
Figure 2-6 Site Features Map
Figure 2-7 Belews Creek Plant Vicinity Map
Figure 2-8 Pre-Ash Basin USGS Topo Map
Figure 2-9 Surface Water Bodies
Figure 2-10 Sample Location Map
Figure 2-11 Belews Creek Steam Station Flow Schematic Diagram
3.0 Source Characteristics
Figure 3-1 Photo of Fly Ash and Bottom Ash
Figure 3-2 Elemental Composition for Bottom Ash, Fly Ash, Shale, and Volcanic Ash
Figure 3-3 Coal Ash TCLP Leachate Concentration vs Regulatory Limits
4.0 Receptor Information
Figure 4-1 USGS Map with Water Supply Wells
Figure 4-2 Water Supply Well Locations
Figure 4-3 Piper Diagram Water Supply Wells
5.0 Regional Geology and Hydrogeology
Figure 5-1 Tectonostratigraphic Map of the Southern and Central Appalachians
Figure 5-2 Regional Geologic Map
Figure 5-3 Piedmont Slope-Aquifer System
6.0 Site Geology
Figure 6-1 Site Geologic Map
Figure 6-2 Site Cross Section Locations
Figure 6-3 General Cross Section A-A'
Figure 6-4 General Cross Section B-B'
Figure 6-5 General Cross Section C-C'
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LIST OF FIGURES CONTINUED
Figure 6-6 Shallow Water Level Map April 2017 - Wet Season
Figure 6-7 Shallow Water Level Map September 2016 - Dry Season
Figure 6-8 Deep Water Level Map April 2017 - Wet Season
Figure 6-9 Deep Water Level Map September 2016 - Dry Season
Figure 6-10 Bedrock Water Level Map April 2017 - Wet Season
Figure 6-11 Bedrock Water Level Map September 2016 - Dry Season
Figure 6-12 Potential Vertical Gradient Between Shallow, Deep, and Bedrock Zones
Figure 6-13 Topographic Lineaments and Rose Diagram
Figure 6-14 Aerial Photography Lineaments and Rose Diagram
7.0 Soil Sampling Results
Figure 7-1 Potential Secondary Source Soil Analytical Results
9.0 Surface Water Results
Figure 9-1 Piper Diagram - AOWs
Figure 9-2 Piper Diagram - Surface Water and Waste Water
10.0 Groundwater Sampling Results
Figure 10-1 Piper Diagram - Shallow Groundwater
Figure 10-2 Piper Diagram - Deep Groundwater
Figure 10-3 Piper Diagram - Bedrock Groundwater
Figure 10-4 Generalized Well Construction Diagram
Figure 10-5 Isoconcentration Map - Antimony In Shallow Groundwater
Figure 10-6 Isoconcentration Map - Antimony In Deep Groundwater
Figure 10-7 Isoconcentration Map - Antimony In Bedrock Groundwater
Figure 10-8 Isoconcentration Map - Arsenic In Shallow Groundwater
Figure 10-9 Isoconcentration Map - Arsenic In Deep Groundwater
Figure 10-10 Isoconcentration Map - Arsenic In Bedrock Groundwater
Figure 10-11 Isoconcentration Map - Barium In Shallow Groundwater
Figure 10-12 Isoconcentration Map - Barium In Deep Groundwater
Figure 10-13 Isoconcentration Map - Barium In Bedrock Groundwater
Figure 10-14 Isoconcentration Map - Beryllium In Shallow Groundwater
Figure 10-15 Isoconcentration Map - Beryllium In Deep Groundwater
Figure 10-16 Isoconcentration Map - Beryllium In Bedrock Groundwater
Figure 10-17 Isoconcentration Map - Boron In Shallow Groundwater
Figure 10-18 Isoconcentration Map - Boron In Deep Groundwater
Figure 10-19 Isoconcentration Map - Boron In Bedrock Groundwater
Figure 10-20 Isoconcentration Map - Cadmium In Shallow Groundwater
Figure 10-21 Isoconcentration Map - Cadmium In Deep Groundwater
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Figure 10-22 Isoconcentration Map - Cadmium In Bedrock Groundwater
Figure 10-23 Isoconcentration Map - Chloride In Shallow Groundwater
Figure 10-24 Isoconcentration Map - Chloride In Deep Groundwater
Figure 10-25 Isoconcentration Map - Chloride In Bedrock Groundwater
Figure 10-26 Isoconcentration Map - Chromium (VI) and Chromium (Total) In Shallow
Groundwater
Figure 10-27 Isoconcentration Map - Chromium (VI) and Chromium (Total) In Deep
Groundwater
Figure 10-28 Isoconcentration Map - Chromium (VI) and Chromium (Total) In Bedrock
Groundwater
Figure 10-29 Isoconcentration Map - Chromium (VI) In Shallow Groundwater
Figure 10-30 Isoconcentration Map - Chromium (VI) In Deep Groundwater
Figure 10-31 Isoconcentration Map - Chromium (VI) In Bedrock Groundwater
Figure 10-32 Isoconcentration Map - Cobalt In Shallow Groundwater
Figure 10-33 Isoconcentration Map - Cobalt In Deep Groundwater
Figure 10-34 Isoconcentration Map - Cobalt In Bedrock Groundwater
Figure 10-35 Isoconcentration Map - Iron In Shallow Groundwater
Figure 10-36 Isoconcentration Map - Iron In Deep Groundwater
Figure 10-37 Isoconcentration Map - Iron In Bedrock Groundwater
Figure 10-38 Isoconcentration Map - Manganese In Shallow Groundwater
Figure 10-39 Isoconcentration Map - Manganese In Deep Groundwater
Figure 10-40 Isoconcentration Map - Manganese In Bedrock Groundwater
Figure 10-41 Isoconcentration Map - Molybdenum In Shallow Groundwater
Figure 10-42 Isoconcentration Map - Molybdenum In Deep Groundwater
Figure 10-43 Isoconcentration Map - Molybdenum In Bedrock Groundwater
Figure 10-44 Isoconcentration Map - Selenium In Shallow Groundwater
Figure 10-45 Isoconcentration Map - Selenium In Deep Groundwater
Figure 10-46 Isoconcentration Map - Selenium In Bedrock Groundwater
Figure 10-47 Isoconcentration Map - Strontium In Shallow Groundwater
Figure 10-48 Isoconcentration Map - Strontium In Deep Groundwater
Figure 10-49 Isoconcentration Map - Strontium In Bedrock Groundwater
Figure 10-50 Isoconcentration Map - Sulfate In Shallow Groundwater
Figure 10-51 Isoconcentration Map - Sulfate In Deep Groundwater
Figure 10-52 Isoconcentration Map - Sulfate In Bedrock Groundwater
Figure 10-53 Isoconcentration Map - Total Dissolved Solids In Shallow Groundwater
Figure 10-54 Isoconcentration Map - Total Dissolved Solids In Deep Groundwater
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Figure 10-55 Isoconcentration Map - Total Dissolved Solids In Bedrock Groundwater
Figure 10-56 Isoconcentration Map - Thallium In Shallow Groundwater
Figure 10-57 Isoconcentration Map - Thallium In Deep Groundwater
Figure 10-58 Isoconcentration Map - Thallium In Bedrock Groundwater
Figure 10-59 Isoconcentration Map - Vanadium In Shallow Groundwater
Figure 10-60 Isoconcentration Map - Vanadium In Deep Groundwater
Figure 10-61 Isoconcentration Map - Vanadium In Bedrock Groundwater
Figure 10-62 Isoconcentration Map - pH In Shallow Groundwater
Figure 10-63 Isoconcentration Map - pH In Deep Groundwater
Figure 10-64 Isoconcentration Map - pH In Bedrock Groundwater
11.0 Hydrogeological Investigation
Figure 11-1 COI vs. Distance- Antimony, Arsenic, Barium, Beryllium, Boron,
Cadmium, Chloride
Figure 11-2 COI vs. Distance- Chromium and Chromium (VI), Cobalt, Iron,
Manganese, Molybdenum, Selenium, Strontium
Figure 11-3 COI vs. Distance- Sulfate, Thallium, Total Dissolved Solids, Vanadium,
pH
Figure 11-4 Antimony Analytical Results - Cross Section A-A'
Figure 11-5 Antimony Analytical Results - Cross Section B-B'
Figure 11-6 Antimony Analytical Results - Cross Section C-C'
Figure 11-7 Arsenic Analytical Results - Cross Section A-A'
Figure 11-8 Arsenic Analytical Results - Cross Section B-B'
Figure 11-9 Arsenic Analytical Results - Cross Section C-C'
Figure 11-10 Barium Analytical Results - Cross Section A-A'
Figure 11-11 Barium Analytical Results - Cross Section B-B'
Figure 11-12 Barium Analytical Results - Cross Section C-C'
Figure 11-13 Beryllium Analytical Results - Cross Section A-A'
Figure 11-14 Beryllium Analytical Results - Cross Section B-B'
Figure 11-15 Beryllium Analytical Results - Cross Section C-C'
Figure 11-16 Boron Analytical Results - Cross Section A-A'
Figure 11-17 Boron Analytical Results - Cross Section B-B'
Figure 11-18 Boron Analytical Results - Cross Section C-C'
Figure 11-19 Cadmium Analytical Results - Cross Section A-A'
Figure 11-20 Cadmium Analytical Results - Cross Section B-B'
Figure 11-21 Cadmium Analytical Results - Cross Section C-C'
Figure 11-22 Chloride Analytical Results - Cross Section A-A'
Figure 11-23 Chloride Analytical Results - Cross Section B-B'
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Figure 11-24 Chloride Analytical Results - Cross Section C-C'
Figure 11-25 Chromium (VI) Analytical Results - Cross Section A-A'
Figure 11-26 Chromium (VI) Analytical Results - Cross Section B-B'
Figure 11-27 Chromium (VI) Analytical Results - Cross Section C-C'
Figure 11-28 Chromium Analytical Results - Cross Section A-A'
Figure 11-29 Chromium Analytical Results - Cross Section B-B'
Figure 11-30 Chromium Analytical Results - Cross Section C-C'
Figure 11-31 Cobalt Analytical Results - Cross Section A-A'
Figure 11-32 Cobalt Analytical Results - Cross Section B-B'
Figure 11-33 Cobalt Analytical Results - Cross Section C-C'
Figure 11-34 Iron Analytical Results - Cross Section A-A'
Figure 11-35 Iron Analytical Results - Cross Section B-B'
Figure 11-36 Iron Analytical Results - Cross Section C-C'
Figure 11-37 Manganese Analytical Results - Cross Section A-A'
Figure 11-38 Manganese Analytical Results - Cross Section B-B'
Figure 11-39 Manganese Analytical Results - Cross Section C-C'
Figure 11-40 Molybdenum Analytical Results - Cross Section A-A'
Figure 11-41 Molybdenum Analytical Results - Cross Section B-B'
Figure 11-42 Molybdenum Analytical Results - Cross Section C-C'
Figure 11-43 pH Analytical Results - Cross Section A-A'
Figure 11-44 pH Analytical Results - Cross Section B-B'
Figure 11-45 pH Analytical Results - Cross Section C-C'
Figure 11-46 Selenium Analytical Results - Cross Section A-A'
Figure 11-47 Selenium Analytical Results - Cross Section B-B'
Figure 11-48 Selenium Analytical Results - Cross Section C-C'
Figure 11-49 Strontium Analytical Results - Cross Section A-A'
Figure 11-50 Strontium Analytical Results - Cross Section B-B'
Figure 11-51 Strontium Analytical Results - Cross Section C-C'
Figure 11-52 Sulfate Analytical Results - Cross Section A-A'
Figure 11-53 Sulfate Analytical Results - Cross Section B-B'
Figure 11-54 Sulfate Analytical Results - Cross Section C-C'
Figure 11-55 Thallium Analytical Results - Cross Section A-A'
Figure 11-56 Thallium Analytical Results - Cross Section B-B'
Figure 11-57 Thallium Analytical Results - Cross Section C-C'
Figure 11-58 TDS Analytical Results - Cross Section A-A'
Figure 11-59 TDS Analytical Results - Cross Section B-B'
Figure 11-60 TDS Analytical Results - Cross Section C-C'
Figure 11-61 Vanadium Analytical Results - Cross Section A-A'
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Figure 11-62 Vanadium Analytical Results - Cross Section B-B'
Figure 11-63 Vanadium Analytical Results - Cross Section C-C'
Figure 11-64 Regional Groundwater Quality - Chloride
Figure 11-65 Regional Groundwater Quality - pH
Figure 11-66 Thallium Distribution in Soil
12.0 Screening-Level Risk Assessment
Figure 12-1 Ecological Exposure Areas
14.0 Discussion - Assessment Results
Figure 14-1 Time vs Concentration - Antimony in Shallow Zone
Figure 14-2 Time vs Concentration - Antimony in Deep Zone
Figure 14-3 Time vs Concentration - Antimony in Bedrock Zone
Figure 14-4 Time vs Concentration - Antimony Pine Hall Road Landfill
Figure 14-5 Time vs Concentration - Arsenic in Shallow Zone
Figure 14-6 Time vs Concentration - Arsenic in Deep Zone
Figure 14-7 Time vs Concentration - Arsenic in Bedrock Zone
Figure 14-8 Time vs Concentration - Arsenic Pine Hall Road Landfill
Figure 14-9 Time vs Concentration - Barium in Shallow Zone
Figure 14-10 Time vs Concentration - Barium in Deep Zone
Figure 14-11 Time vs Concentration - Barium in Bedrock Zone
Figure 14-12 Time vs Concentration - Barium Pine Hall Road Landfill
Figure 14-13 Time vs Concentration - Beryllium in Shallow Zone
Figure 14-14 Time vs Concentration - Beryllium in Deep Zone
Figure 14-15 Time vs Concentration - Beryllium in Bedrock Zone
Figure 14-16 Time vs Concentration - Beryllium Pine Hall Road Landfill
Figure 14-17 Time vs Concentration - Boron in Shallow Zone
Figure 14-18 Time vs Concentration - Boron in Deep Zone
Figure 14-19 Time vs Concentration - Boron in Bedrock Zone
Figure 14-20 Time vs Concentration - Boron Pine Hall Road Landfill
Figure 14-21 Time vs Concentration - Cadmium in Shallow Zone
Figure 14-22 Time vs Concentration - Cadmium in Deep Zone
Figure 14-23 Time vs Concentration - Cadmium in Bedrock Zone
Figure 14-24 Time vs Concentration - Cadmium Pine Hall Road Landfill
Figure 14-25 Time vs Concentration - Chloride in Shallow Zone
Figure 14-26 Time vs Concentration - Chloride in Deep Zone
Figure 14-27 Time vs Concentration - Chloride in Bedrock Zone
Figure 14-28 Time vs Concentration - Chloride Pine Hall Road Landfill
Figure 14-29 Time vs Concentration - Chromium and Chromium (VI) in Shallow Zone
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Figure 14-30 Time vs Concentration - Chromium and Chromium (VI) in Deep Zone
Figure 14-31 Time vs Concentration - Chromium and Chromium (VI) in Bedrock Zone
Figure 14-32 Time vs Concentration - Chromium Pine Hall Landfill
Figure 14-33 Time vs Concentration - Cobalt in Shallow Zone
Figure 14-34 Time vs Concentration - Cobalt in Deep Zone
Figure 14-35 Time vs Concentration - Cobalt in Bedrock Zone
Figure 14-36 Time vs Concentration - Cobalt Pine Hall Landfill
Figure 14-37 Time vs Concentration - Iron in Shallow Zone
Figure 14-38 Time vs Concentration - Iron in Deep Zone
Figure 14-39 Time vs Concentration - Iron in Bedrock Zone
Figure 14-40 Time vs Concentration - Iron Pine Hall Landfill
Figure 14-41 Time vs Concentration - Manganese in Shallow Zone
Figure 14-42 Time vs Concentration - Manganese in Deep Zone
Figure 14-43 Time vs Concentration - Manganese in Bedrock Zone
Figure 14-44 Time vs Concentration - Manganese Pine Hall Landfill
Figure 14-45 Time vs Concentration - Molybdenum in Shallow Zone
Figure 14-46 Time vs Concentration - Molybdenum in Deep Zone
Figure 14-47 Time vs Concentration - Molybdenum in Bedrock Zone
Figure 14-48 Time vs Concentration - Molybdenum Pine Hall Landfill
Figure 14-49 Time vs Concentration - pH in Shallow Zone
Figure 14-50 Time vs Concentration - pH in Deep Zone
Figure 14-51 Time vs Concentration - pH in Bedrock Zone
Figure 14-52 Time vs Concentration - pH Pine Hall Landfill
Figure 14-53 Time vs Concentration - Selenium in Shallow Zone
Figure 14-54 Time vs Concentration - Selenium in Deep Zone
Figure 14-55 Time vs Concentration - Selenium in Bedrock Zone
Figure 14-56 Time vs Concentration - Selenium Pine Hall Landfill
Figure 14-57 Time vs Concentration - Strontium in Shallow Zone
Figure 14-58 Time vs Concentration - Strontium in Deep Zone
Figure 14-59 Time vs Concentration - Strontium in Bedrock Zone
Figure 14-60 Time vs Concentration - Strontium Pine Hall Landfill
Figure 14-61 Time vs Concentration - Sulfate in Shallow Zone
Figure 14-62 Time vs Concentration - Sulfate in Deep Zone
Figure 14-63 Time vs Concentration - Sulfate in Bedrock Zone
Figure 14-64 Time vs Concentration - Sulfate Pine Hall Landfill
Figure 14-65 Time vs Concentration - TDS in Shallow Zone
Figure 14-66 Time vs Concentration - TDS in Deep Zone
Figure 14-67 Time vs Concentration - TDS in Bedrock Zone
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Figure 14-68 Time vs Concentration - TDS Pine Hall Landfill
Figure 14-69 Time vs Concentration - Thallium in Shallow Zone
Figure 14-70 Time vs Concentration - Thallium in Deep Zone
Figure 14-71 Time vs Concentration - Thallium in Bedrock Zone
Figure 14-72 Time vs Concentration - Thallium Pine Hall Landfill
Figure 14-73 Time vs Concentration - Vanadium in Shallow Zone
Figure 14-74 Time vs Concentration - Vanadium in Deep Zone
Figure 14-75 Time vs Concentration - Vanadium in Bedrock Zone
Figure 14-76 Time vs Concentration - Vanadium Pine Hall Landfill
Figure 14-77 Groundwater Concentration Trend Analysis - Antimony All Flow Layers
and AOWs
Figure 14-78 Groundwater Concentration Trend Analysis - Arsenic All Flow Layers
and AOWs
Figure 14-79 Groundwater Concentration Trend Analysis - Barium All Flow Layers and
AOWs
Figure 14-80 Groundwater Concentration Trend Analysis - Beryllium All Flow Layers
and AOWs
Figure 14-81 Groundwater Concentration Trend Analysis - Boron All Flow Layers and
AOWs
Figure 14-82 Groundwater Concentration Trend Analysis - Cadmium All Flow Layers
and AOWs
Figure 14-83 Groundwater Concentration Trend Analysis - Chloride All Flow Layers
and AOWs
Figure 14-84 Groundwater Concentration Trend Analysis - Chromium (VI) All Flow
Layers and AOWs
Figure 14-85 Groundwater Concentration Trend Analysis - Chromium (Total) All Flow
Layers and AOWs
Figure 14-86 Groundwater Concentration Trend Analysis - Cobalt All Flow Layers and
AOWs
Figure 14-87 Groundwater Concentration Trend Analysis - Iron All Flow Layers and
AOWs
Figure 14-88 Groundwater Concentration Trend Analysis - Manganese All Flow Layers
and AOWs
Figure 14-89 Groundwater Concentration Trend Analysis - Molybdenum All Flow
Layers and AOWs
Figure 14-90 Groundwater Concentration Trend Analysis - pH All Flow Layers and
AOWs
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Figure 14-91 Groundwater Concentration Trend Analysis - Selenium All Flow Layers
and AOWs
Figure 14-92 Groundwater Concentration Trend Analysis - Strontium All Flow Layers
and AOWs
Figure 14-93 Groundwater Concentration Trend Analysis - Sulfate All Flow Layers and
AOWs
Figure 14-94 Groundwater Concentration Trend Analysis - Total Dissolved Solids All
Flow Layers and AOWs
Figure 14-95 Groundwater Concentration Trend Analysis - Thallium All Flow Layers
and AOWs
Figure 14-96 Groundwater Concentration Trend Analysis - Vanadium All Flow Layers
and AOWs
Figure 14-97 Comprehensive Groundwater Data
Figure 14-98 Comprehensive Surface Water and Seep Data
Figure 14-99 Comprehensive Soil and Sediment Data
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LIST OF TABLES
2.0 Site History and Description
Table 2-1 Well Construction Data
Table 2-2 Compliance Monitoring Wells
Table 2-3 Summary of Onsite Environmental Incidents
3.0 Source Characteristics
Table 3-1 Range (10th percentile - 90th percentile) in Bulk Composition of Fly Ash,
Bottom Ash, Rock, and Soil (Source: EPRI 2009a)
Table 3-2 Soil/Material Properties for Ash, Fill, Alluvium, and Soil/Saprolite
Table 3-3 Regional Background Soil SPLP data
4.0 Receptor Information
Table 4-1 Public and Private Water Supply Wells within 0.5-mile Radius of Ash
Basin Compliance Boundary'
Table 4-2 Property Owner Addresses Contiguous to the Ash Basin Waste Boundary
Table 4-3 Private Water Supply Analytical Results
Table 4-4 Piedmont Groundwater Background Threshold Values
6.0 Site Geology
Table 6-1 Soil Mineralogy Results
Table 6-2 Soil Chemistry Results - Oxides
Table 6-3 Soil Chemistry Results - Elemental
Table 6-4 Solid Matrix Parameters and Analytical Methods for Soil, Ash, and Rock
Parameters and Constituent Analysis - Analytical Methods
Table 6-5 Ash Basin Surface Water, Pore water and Seep Parameters and Analytical
Methods
Table 6-6 Transition Zone Mineralogy
Table 6-7 Oxide Composition of Transition Zone Samples
Table 6-8 Elemental Composition of Transition Zone Samples
Table 6-9 Whole Rock Chemistry Results - Oxides
Table 6-10 Whole Rock Chemistry Results - Elemental
Table 6-11 Petrographic Analysis Summary
Table 6-12 Historic and Recent Water Level Measurements
Table 6-13 Horizontal Groundwater Gradients and Flow Velocities
Table 6-14 Vertical Hydraulic Gradients
Table 6-15 Hydrostratigraphic Layer Properties - Horizontal Hydraulic Conductivity
Table 6-16 Hydrostratigraphic Layer Properties - Vertical Hydraulic Conductivity
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LIST OF TABLES CONTINUED
Table 6-17 In-Situ Hydraulic Conductivity Results
Table 6-18 Estimated Effective Porosity/Specific Yield and Specific Storage for Upper
Hydrostratigraphic Units (A, F, S, M1, and M2)
Table 6-19 Total Porosity, Secondary (Effective) Porosity/Specific Yield, and Specific
Storage for Lower Hydrostratigraphic Units (TZ and BR)
Table 6-20 Field Permeability Test Results
Table 6-21 Historic Laboratory Field Permeability Test Results
7.0 Soil Sampling Results
Table 7-1 Unsaturated Background Soil Data Summary
Table 7-2 Provisional Background Threshold Values for Soil
10.0 Groundwater Sampling Results
Table 10-1 Background Groundwater Results Through April 2017
Table 10-2 Groundwater Provisional Background Threshold Values
Table 10-3 State and Federal Standards for COIs
11.0 Hydrogeological Investigation
Table 11-1 Private Well Sample Results
13.0 Groundwater Modeling Results
Table 13-1 Summary of Kd Values from Batch and Column Studies
15.0 Conclusions and Recommendations
Table 15-1 Groundwater Interim Monitoring Program Analytical Methods
Table 15-2 Interim Monitoring Program List
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LIST OF APPENDICES
Appendix A Regulatory Correspondence
DEQ Expectations Document (July 18, 2017)
Completed DEQ CSA Update Expectations Check List
NCDENR NORR Letter (August 13, 2014)
Revised Interim Monitoring Plans for 14 Duke Energy Facilities
(October 19, 2017)
NCDEQ Background Dataset Review (July 7, 2017)
NCDEQ Background Dataset Review (September 1, 2017)
NCDEQ Background Threshold Value Approval Attachments
(September 1, 2017)
Appendix B Comprehensive Data Table
Appendix B Notes
Table 1 - Groundwater Results
Table 2 - Surface Water Results
Table 3 - AOW and WW Results
Table 4 - Soil and Ash Results
Table 5 - Sediment Results
Table 6 - SPLP Results
Appendix C Site Assessment Data
HDR CSA Appendix H
Soil Physical Lab Reports
Mineralogy Lab Reports
Slug Test Procedure
Slug Test Reports
Historic Permeability Data
Field Permeability Data
Fetter-Bear Diagrams – Porosity
Historic Porosity Data
Estimated Seasonal High Groundwater Elevations Calculation
HDR CSA Supplement 2 Slug Test Report
UNCC Soil Sorption Evaluation
Addendum to the UNCC Soil Sorption Evaluation
Appendix D Receptor Surveys
Updated Receptor Survey Report
Supplement to Drinking Water Well and Receptor Survey
Drinking Water Supply Well and Receptor Survey
Dewberry Report – Permanent Water Supply Proposal to DEQ
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LIST OF APPENDICES CONTINUED
Appendix E Supporting Documents
Stantec Report
WSP Maps
Appendix F Boring Logs, Construction Diagrams, and Abandonment Records
Well Boring Logs
Well Construction Records
Well Abandonment Records
Soil Sample and Rock Core Photos
Appendix G Methodology
Source Characterization
Soil and Rock Characterization
Surface water and sediment characterization
Groundwater characterization
Field, Sampling, and Data analysis Quality Assurance / Quality
Control
Appendix H Background Determination
Belews Creek 2017 CSA PBTV Report
HDR Background Determination Report
Appendix I Lab Reports
Water Supply Wells 2015
Round 2 - Surface Water
Round 2 - September 2015
Round 3 - November 2015
Round 4 - December 2015
Round 5 - March and April 2016
Round 6 - May 2016
Round 7 - September 2016
Round 8 - November 2016
Round 9 - January 2017
Round 10 - April 2017
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LIST OF ACRONYMS
2B NCDENR Title 15A, Subchapter 02B. Surface Water and Wetland
Standards
2L NCDENR Title 15A, Subchapter 02L. Groundwater Classification and
Standards
ADD Average Daily Dose
AOW Area of Wetness
ASTM American Society for Testing and Materials
BCSS Belews Creek Steam Station
BGS Below Ground Surface
BOD Basis of Design
BR Bedrock
CAMA Coal Ash Management Act
CAP Corrective Action Plan
CCR Coal Combustion Residuals
CFR Code of Federal Register
CM/SEC Centimeters per second
COI Constituent of Interest
CSA Comprehensive Site Assessment
DO Dissolved Oxygen
DOE Department of Energy
Duke Energy Duke Energy Carolinas, LLC
DWM Division of Waste Management
EDR Environmental Database Resources, Inc.
EMP Effectiveness Monitoring Program
EPC Exposure Point Concentration
EPD Environmental Protection Division
EPRI Electric Power Research Institute
FGD Flue Gas Desulfurization
GAP Groundwater Assessment Work Plan
GIS Geographic Information System
GPD Gallons Per Day
GTB Geotechnical Borings
HAO Hydrous Aluminum Oxide
HB Highway Business District
HDPE High-Density Polyethylene
HFO Hydrous Ferric Oxide
HSSR Hydrogeochemical and Stream Sediment Reconnaissance
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LIST OF ACRONYMS CONTINUED
IAP Interim Action Plan
IMAC Interim Maximum Allowable Concentration
IMP Interim Monitoring Plan
Kd Sorption Coefficient
LOAEL Lowest Observed Adverse Effects Level
MCL Maximum Contaminant Level
Mg/kg Milligrams per Kilogram
Mg/L Milligrams per liter
MGD Million Gallons per Day
Mil Thousandths of Inch
mm Millimeter
MNA Monitored Natural Attenuation
MRL Method Reporting Limit
MT3DMS Modular 3-D Transport Multi-Species
MW Megawatts
NAVD 88 North American Vertical Datum of 1988
NCAC North Carolina Administrative Code
NCDENR North Carolina Department of Environment and Natural Resources
NCDEQ North Carolina Department of Environmental Quality
NCDHHS North Carolina Department of Health and Human Services
NORR Notice of Regulatory Requirements
NPDES National Pollutant Discharge Elimination System
NSDWRs National Secondary Drinking Water Regulations
NURE National Uranium Resource Evaluation
PBTV Provisional Background Threshold Value *Define on p. ES-4
Plant/Site Belews Creek Steam Station
PMCL Primary Maximum Contaminant Level
POG Protection of Groundwater
PPB Parts per billion
PPBC Proposed Provisional Background Concentrations
PSRG Preliminary Soil Remediation Goal
PWR Partially Weathered Rock
RBC Risk-Based Concentrations
REC Recovery
RQD Rock Quality Designation
RSL Regional Screening Levels
S.U. Standard Units
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LIST OF ACRONYMS CONTINUED
SCM Site Conceptual Model
SMCL Secondary Maximum Contaminant Level
SPLP Synthetic Precipitation Leaching Procedure
SW Surface Water
SWAP Source Water Assessment Program
TCLP Toxicity Characteristic Leaching Procedure
TDS Total Dissolved Solids
TOC Total Organic Carbon
TRVs Toxicity Reference Values
TZ Transition Zone
UMC United Methodist Church
UNC University of North Carolina
UNCC University of North Carolina at Charlotte
USEPA United States Environmental Protection Agency
USCS Unified Soil Classification System
USDA U.S. Department of Agriculture
USGS United States Geological Survey
UTL Upper Tolerance Limit
Work Plan Groundwater Assessment Work Plan
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1.0 INTRODUCTION
Duke Energy Carolinas, LLC (Duke Energy) owns and operates the Belews Creek Steam
Station (BCSS), which is located on Belews Reservoir in Belews Creek, Stokes County,
North Carolina (Figure 1-1). BCSS began operation in 1974 as a coal-fired generating
station and currently operates two coal-fired units with 2,240 megawatt capacity of
generation. Coal combustion residuals (CCR) have historically been managed in the
Site’s ash basin (surface impoundment) located north of Pine Hall Road to the west-
northwest of the station. CCR were initially deposited in the ash basin by hydraulic
sluicing operations. In 1984, BCSS converted from a wet to a dry fly ash handling
system. However, the ability to sluice to the ash basin was still available, but limited to
certain situations (i.e. unit startup/shutdown, equipment maintenance and service). A
100% dry ash handling system is currently being constructed onsite. Discharge from
the ash basin to the Dan River is permitted by the North Carolina Department of
Environmental Quality (NCDEQ)1 Division of Water Resources (DWR) under the
National Pollutant Discharge Elimination System (NPDES) Permit NC0024406.
Purpose of Comprehensive Site Assessment 1.1
This Comprehensive Site Assessment (CSA) update was conducted to refine and
expand the understanding of subsurface geologic/hydrogeologic conditions and
evaluate the extent of impacts from historical management of coal ash in the ash basin.
This CSA update contains an assessment of Site conditions based on a comprehensive
interpretation of geologic and sampling results from the initial Site assessment and
geologic and sampling results obtained subsequent to the initial assessment and has
been prepared in coordination with Duke Energy and NCDEQ in response to requests
for additional information, including additional sampling and assessment of specified
areas.
This CSA update was prepared in conformance to the most recently updated CSA table
of contents provided by NCDEQ to Duke Energy on September 29, 2017. In response to
a request from NCDEQ for an updated CSA report, this submittal includes the
following information. The NCDEQ Expectations Document (July 18, 2017) and the
completed NCDEQ CSA Update Expectations Check List are included in Appendix A:
Review of baseline assessment data collected and reported as part of CSA
activities;
1 Prior to September 18, 2015, the NCDEQ was referred to as the North Carolina Department of Environment and
Natural Resources (NCDENR). Both naming conventions are used in this report, as appropriate.
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A summary of NPDES and Coal Ash Management Act (CAMA) groundwater
monitoring information;
A summary of potential receptors including analytical results from water supply
wells;
A description and findings of additional assessment activities conducted since
submittal of the CSA Supplement report(s);
An update on background concentrations for groundwater and soil; and,
Definition of horizontal and vertical extent of CCR constituents in soil and
groundwater based upon NCDEQ approved background concentrations.
An update to human health and ecological risk assessment to evaluate the
existence of imminent hazards to public health, safety and the environment.
Regulatory Background 1.2
The North Carolina Coal Ash Management Act of 2014 (CAMA) directs owners of CCR
surface impoundments in North Carolina to conduct groundwater monitoring,
assessment, and remedial activities, if necessary. The CSA was performed to collect
information necessary to evaluate the horizontal and vertical extent of impacts to soil
and groundwater attributable to CCR source area(s), identify potential receptors, and
screen for potential risks to those receptors.
Notice of Regulatory Requirements (NORR) 1.2.1
On August 13, 2014, NCDENR issued a Notice of Regulatory Requirements
(NORR) letter notifying Duke Energy that exceedances of groundwater quality
standards were reported at 14 coal ash facilities owned and operated by Duke
Energy. Those groundwater quality standards are part of 15A NCAC 02L (2L)
.0200 Classifications and Water Quality Standards Applicable to the
Groundwaters of North Carolina. The NORR stipulated that for each coal ash
facility, Duke Energy was to conduct a CSA. The NORR also stipulated that
before conducting each CSA, Duke was to submit a Groundwater Assessment
Work Plan (GAP or Work Plan) and a receptor survey. In accordance with the
NORR requirements, a receptor survey was performed to identify all receptors
within a 0.5-mile radius (2,640 feet) of the ash basin compliance boundary, and a
CSA was conducted for each facility. The NORR letter is included in Appendix
A.
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Coal Ash Management Act Requirements 1.2.2
The Coal Ash Management Act (CAMA) of 2014 — General Assembly of North
Carolina Senate Bill 729 Ratified Bill (Session 2013) (SB 729) requires that ash
from Duke Energy coal plant sites located in North Carolina either (1) be
excavated and relocated to fully lined storage facilities or (2) go through a
classification process to determine closure options and schedule. Closure options
can include a combination of excavating and relocating ash to a fully lined
structural fill, excavating and relocating the ash to a lined landfill (on-site or off-
site), and/or capping the ash with an engineered synthetic barrier system, either
in place or after being consolidated to a smaller area on-site.
As a component of implementing this objective, CAMA provides instructions for
owners of coal combustion residuals surface impoundments to perform various
groundwater monitoring and assessment activities. Section §130A-309.209 of the
CAMA ruling specifies groundwater assessment and corrective actions, drinking
water supply well surveys and provisions of alternate water supply, and
reporting requirements as follows:
(a) Groundwater Assessment of Coal Combustion Residuals Surface
Impoundments. – The owner of a coal combustion residuals surface
impoundment shall conduct groundwater monitoring and assessment as
provided in this subsection. The requirements for groundwater monitoring
and assessment set out in this subsection are in addition to any other
groundwater monitoring and assessment requirements applicable to the
owners of coal combustion residuals surface impoundments.
(1) No later than December 31, 2014, the owner of a coal combustion
residuals surface impoundment shall submit a proposed Groundwater
Assessment Plan for the impoundment to the Department for its review
and approval. The Groundwater Assessment Plan shall, at a minimum,
provide for all of the following:
a. A description of all receptors and significant exposure pathways.
b. An assessment of the horizontal and vertical extent of soil and
groundwater contamination for all contaminants confirmed to be
present in groundwater in exceedance of groundwater quality
standards.
c. A description of all significant factors affecting movement and
transport of contaminants.
d. A description of the geological and hydrogeological features
influencing the chemical and physical character of the
contaminants.
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2) The Department shall approve the Groundwater Assessment Plan if it
determines that the Plan complies with the requirements of this
subsection and will be sufficient to protect public health, safety, and
welfare; the environment; and natural resources.
(3) No later than 10 days from approval of the Groundwater Assessment
Plan, the owner shall begin implementation of the Plan.
(4) No later than 180 days from approval of the Groundwater Assessment
Plan, the owner shall submit a Groundwater Assessment Report to the
Department. The Report shall describe all exceedances of groundwater
quality standards associated with the impoundment.
Approach to Comprehensive Site Assessment 1.3
The CSA has been performed to meet NCDEQ requirements associated with potential
site remedy selection. The following components were utilized to develop the
assessment.
NORR Guidance 1.3.1
The NORR requires that the site assessment provide information to meet the
requirements of North Carolina regulation 2L .0106 (g). This regulation lists the
items to be included in site assessments conducted pursuant to Paragraph (c) of
the rule. These requirements are listed below and referenced to the applicable
sections of this CSA.
15A NCAC 02L .0106(g) Requirement CSA Section(s)
(1) The source and cause of contamination; Section 3.0
(2) Any imminent hazards to public health and
safety, as defined in G.S. 130A-2, and any
actions taken to mitigate them in accordance
with Paragraph (f) of this Rule;
Sections ES.2 and 2.8
(3) All receptors and significant exposure
pathways; Sections 4.0 and 12.0
(4) The horizontal and vertical extent of soil and
groundwater contamination and all
significant factors affecting contaminant
transport; and
Section 7.0, 8.0, and 14.0
(5) Geological and hydrogeological features
influencing the movement, chemical, and
physical character of the contaminants.
Section 6.0, 11.0, and 15.0
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USEPA Monitored Natural Attenuation Tiered Approach 1.3.2
The assessment data is compiled in a manner to be consistent with “Monitored
Natural Attenuation of Inorganic Contaminants in Groundwater” (USEPA,
October 2007). The tiered analysis approach discussed in this guidance
document is designed to align site characterization tasks to reduce uncertainty in
remedy selection. The tiered assessment data collection includes information to
evaluate:
Active contaminant removal from groundwater and dissolved plume
stability,
The mechanisms and rates of attenuation,
The long-term capacity for attenuation and stability of immobilized
contaminants, and
Anticipated performance monitoring needs to support the selected
remedy.
ASTM Conceptual Site Model Guidance 1.3.3
The American Society for Testing and Materials (ASTM) E1689-95 generally
describes the major components of conceptual site models, including an outline
for developing models. To the extent possible, this guidance was incorporated
into preparation of the Site Conceptual Model presented in Section 14.0. The Site
Conceptual Model is used to integrate site information, identify data gaps, and
determine whether additional information is needed at the site. The model is also
used to facilitate selection of remedial alternatives and evaluate the potential
effectiveness of remedial actions in reducing the exposure of environmental
receptors to contaminants (ASTM, 2014).
Technical Objectives 1.4
The rationale for CSA activities fall into one of the following categories:
Determine the range of background groundwater quality from pertinent geologic
settings (horizontal and vertical) across a broad area of the Site.
Evaluate groundwater quality from pertinent geologic settings (horizontal and
vertical extent of CCR leachate constituents).
Establish perimeter (horizontal and vertical) boundary conditions for
groundwater modeling.
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Provide source area information including ash pore water chemistry, physical
and hydraulic properties, CCR thickness and residual saturation within the ash
basin.
Address soil chemistry in the vicinity of the ash basin (horizontal and vertical
extent of CCR leachate constituents in soil) compared to background
concentrations.
Determine potential routes of exposure and receptors.
Compile information necessary to develop a groundwater Corrective Action Plan
(CAP) protective of human health and the environment in accordance with 2L.
Previous Submittals 1.5
Detailed descriptions of the Site operational history, the Site conceptual model, physical
setting and features, geology/hydrogeology, and results of the findings of the CSA and
other CAMA-related works are documented in full in the following:
Comprehensive Site Assessment Report – Belews Creek Steam Station Ash Basin (HDR
Engineering, Inc. of the Carolinas (HDR, 2015a).
Corrective Action Plan Part 1 – Belews Creek Steam Station Ash Basin (HDR, 2015b).
Corrective Action Plan Part 2 (included CSA Supplement 1 as Appendix A) – Belews
Creek Steam Station Ash Basin (HDR, 2016d).
Comprehensive Site Assessment Supplement 2 – Belews Creek Steam Station Ash Basin
(HDR, 2016c).
Basis of Design Report (100% Submittal) – Belews Creek Steam Station (SynTerra,
2017a).
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2.0 SITE HISTORY AND DESCRIPTION
An overview of the BCSS setting and operations is presented in the following sections.
Site Description, Ownership and Use History 2.1
The BCSS site is located on the north side of Belews Reservoir on Pine Hall Road in
Belews Creek, Stokes County, North Carolina. BCSS is one of Duke Energy's largest
coal-burning power plants in the Carolinas. BCSS is a two-unit coal-fired electricity
generating plant with a capacity of 2,240 megawatts (MW).
The BCSS site, including the station and supporting facilities, is approximately 700 acres
(Figure 2-1). The BCSS site lies within a 6,100 acre parcel owned by Duke Energy, of
which, Belews Reservoir comprises 3,800 acres and extends into Rockingham, Guilford
and Forsyth counties. Based on a review of available historical aerial photography, the
Site consisted of a combination of agricultural land, rural residential, and woodlands
prior to the impoundment of Belews Creek for the formation of Belews Reservoir.
Aerial photographs from 1951, 1966, 1971, and 1977 are presented as Figures 2-2, 2-3, 2-
4, and 2-5, respectively. The station began commercial operations in 1974 with Unit 1
(1,120 MW) followed by Unit 2 (1,120 MW) in 1975. Four generators are present at
BCSS, including two low pressure generators and two high pressure/intermediate
pressure generators. Cooling water for BCSS is provided by Belews Reservoir.
The air pollution control system for the coal-fired units at BCSS includes a selective
catalytic reducer to remove nitrogen oxide emissions, an electrostatic precipitator that
removes fly ash, and the units have low nitrogen oxide burners in the boiler. A Flue Gas
Desulfurization (FGD) system is active at BCSS. The FGD system directs flue gas into
an absorber where limestone (calcium carbonate) slurry is sprayed. Sulfur dioxide in
the flue gas reacts with the limestone slurry to produce calcium sulfate, or gypsum.
Gypsum is primarily sold for re-use or managed in the on-site NCDEQ Division of
Waste Management (DWM) approved FGD Residue Landfill (Permit No. 8505).
The BCSS ash basin is located across Pine Hall Road to the northwest of the station and
is generally bounded by an earthen dam and a natural ridge to the north, Middleton
Loop Road to the west, and Pine Hall Road to the south and east (Figure 2-1).
Middleton Loop Road and Pine Hall Road are located along topographic divides.
Topography to the west of Middleton Loop Road and north of the earthen dam and
natural ridge generally slopes downward toward the Dan River. Topography to the
south and east of Pine Hall Road generally slopes downward toward Belews Reservoir.
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Other areas of the site are occupied by facilities supporting the production or
transmission of power, including a switchyard, substation, and associated transmission
lines. A former chemical holding pond (the pond has been drained and the valve left
open to allow surface flow of storm water through) is located in the southeast end of the
ash basin. The drained pond is now part of the ash basin. The closed Pine Hall Road
Landfill (NCDEQ Permit No. 8503) is located south of the ash basin and north of Pine
Hall Road. An structural fill constructed using fly ash generated from BCSS under the
structural fill rules found in 15A NCAC 13B .1700 is located south of the ash basin on
the south side of Pine Hall Road. The structural fill was approved by the NCDEQ
DWM (Permit No. CCB0070). The Craig Road Landfill (NCDEQ Permit No. 8504) and
the FGD Residue Landfill (NCDEQ Permit No. 8505) are located south of the ash basin
on the south side of Belews Reservoir. Site features are shown on Figure 2-6.
Geographic Setting, Surrounding Land Use, Surface Water 2.2
Classification
The BCSS site is situated in a rural area along Belews Reservoir in Stokes County, North
Carolina. A description of the physical setting for BCSS is provided in the following
sections.
Geographic Setting
The surrounding area around BCSS generally consists of residential properties, farm
land, undeveloped land, and Belews Reservoir (Figure 2-7). Natural topography at the
BCSS site ranges from an approximate high elevation of 878 feet (NAVD 88) southeast
of the ash basin near the intersection of Pine Hall Road and Middleton Loop Road to an
approximate low elevation of 646 feet at the base of the earthen dike located at the north
end of the ash basin. The ash basin designated effluent channel extends from the base of
the ash basin dam and flows approximately 4,400 feet from southeast to northwest
where it enters the Dan River. The elevation at the discharge point of the tributary to
the Dan River is approximately 578 feet. The elevation of Belews Reservoir is
approximately 725 feet. A 1962 United States Geological Survey (USGS) topographic
map depicting the site prior to construction of the ash basin features is shown on Figure
2-8. The Pine Hall Road Landfill is located upgradient to the ash basin and is just north
of the Pine Hall Road topographic divide. The BCSS structural fill is located south of
the BCSS ash basin and Pine Hall Road. Refer to Section 3.1 for a detailed description of
the BCSS ash basin and other ash storage facilities.
Surrounding Land Use
Properties located within the 0.5-mile radius of the BCSS ash basin compliance
boundary generally consist of residential properties located to the southwest and
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residential farm land northeast, north, and west. Duke Energy property is located to the
north, northwest, south, and east with Belews Reservoir beyond to the south and east.
A review of deed information for properties surrounding the BCSS site indicates most
of these properties do not currently have a Stokes County zoning designation. The
Duke Energy property is zoned Light Manufacturing District (M-1) where the principal
use is for light manufacturing and warehousing which normally seek locations on large
tracts of land where the operations involved do not detract from the development
potential of nearby undeveloped properties. Another parcel located north of the Dan
River from the BCSS site is also zoned M-1 and is owned by a pipe and brick company.
The only other zoned parcel in the vicinity of the BCSS site is located on the south side
of Pine Hall Road and west of the Pine Hall Road Landfill. This property is zoned
Highway Business District (HB) which allows the property to be used for retail trade
establishments and the provision of services to the traveling public.
Meteorological Setting
In summer, the average temperature in Stokes County is 74°F, and the average daily
maximum temperature is 85°F (USDA-NRCS 1995). In winter, the average temperature
is 37°F, and the average daily minimum temperature is 25°F. The total annual
precipitation in Stokes County is 45 inches, with approximately half (24 inches)
occurring from April through September. Thunderstorms occur approximately 46 days
each year (U.S. Department of Agriculture, 1995). The average relative humidity in
midafternoon is approximately 55 percent, with humidity reaching higher levels at
night. The prevailing wind is from the southwest, and average wind speed is highest (9
miles per hour) in spring (U.S. Department of Agriculture, 1995).
Surface Water Classification
The BCSS site drains to the Dan River which is part of the Roanoke River watershed.
The Site is located between Belews Reservoir to the south and the Dan River to the
north. The ash basin designated effluent channel extends from the base of the ash basin
dam and flows northwards through Duke Energy property where it discharges to the
Dan River (NPDES outfall 003). This feature was designated as a designated effluent
channel by the State of North Carolina in the 1980’s when the ash pond discharge was
redirected from Belews Reservoir to the Dan River.
Surface water classifications in North Carolina are defined in 15A NCAC 02B.0101(c).
The surface water classification for the Dan River and Belews Reservoir in the vicinity
of the BCSS site is Class WS-IV and Class WS-IV–C, respectively. Class WS-IV waters
are protected as water supplies which are generally in moderately to highly developed
watersheds. Class C waters are protected for uses such as secondary recreation, fishing,
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wildlife, fish consumption, aquatic life including propagation, and survival. Surface
water features located on the site are shown on Figure 2-9.
No residential potable water supply lines are available to the area, with the nearest
residential water supply line, provided by the Town of Walnut Cove, located at the
intersection of Martin-Luther King Jr. Road and Crestview Drive, approximately 4.5
miles to the west from the Duke Power Steam Plant Road entrance to the Station. BCSS
is supplied with potable water from water lines originating south of the plant by the
City of Winston-Salem.
No surface water intakes, other than the intake used to pump water from Belews
Reservoir for BCSS plant operations, the intake on Belews Reservoir to pump water for
water trucks at the Craig Road Landfill, and the backup intake on the Dan River, are
located in the vicinity of BCSS either in Belews Reservoir or in the Dan River.
CAMA-related Source Areas 2.3
CAMA provides for groundwater assessment of CCR surface impoundments defined as
topographic depressions, excavations, or diked areas formed primarily of earthen
materials, without a base liner, and that meet other criteria related to design, usage, and
ownership (Section §130A-309.201).
At BCSS, the groundwater assessment was conducted for the ash basin CCR surface
impoundment, including the former chemical pond and the Pine Hall Road Landfill
(NCDEQ Permit No. 8503-INDUS). Figure 2-10 shows all sample locations regarding
assessment activities. Collectively, the ash basin, the former chemical pond, and the
Pine Hall Road Landfill are referred to herein as ash management areas.
The BCSS ash basin consists of a single cell impounded by an earthen dam located on
the north end of the ash basin. The dam is approximately 2,000 feet long and a
maximum of approximately 140 feet high. The top of the dam is at elevation 770 feet
and the crest is 20 feet wide. The ash basin was constructed from 1970 to 1972 and is
located approximately 3,200 feet northwest of the BCSS powerhouse. The area
contained within the ash basin waste boundary is approximately 283 acres. The full
pond elevation of the BCSS ash basin is approximately 750 feet. The full pond capacity
of the ash basin is estimated to be 17,656,000 cubic yards (cy).
The Pine Hall Road Landfill received a permit to operate on December 10, 1984 and a
subsequent expansion (Phase I Expansion) was permitted in 2003. The unlined landfill
is a monofill that was permitted to receive fly ash from the combustion of coal at BCSS.
The total footprint of the landfill is approximately 52 acres. The placement of ash
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within the Phase I expansion was discontinued prior to March 2008. A total of
approximately 8,500,000 cubic yards (cy) of ash was placed within the Pine Hall Road
Landfill between December 1984 and March 2008.
More detailed discussion of the ash management areas is provided in Section 3.0 of this
report.
Regulation 15A NCAC 02L .0106 (f)(4) requires that the secondary sources that could be
potential continuing sources of possible pollutants to groundwater be addressed in the
CAP. At the BCSS, the soil located below the ash basin could be considered a potential
CAMA-related secondary source. Information to date indicates that the thickness of soil
impacted by ash would generally be limited to the depth interval near the ash/soil
interface.
Other Primary and Secondary Sources 2.4
CSA activities, as outlined in the NCDENR NORR letter, included an assessment of the
horizontal and vertical extent of constituents related to the ash management areas
observed at concentrations greater than the 2L Standards/Interim Maximum Allowable
Concentrations (IMACs) or background concentrations. If the CSA indicates constituent
exceedances are related to sources other than the CCR impoundments, these sources
will be addressed as part of a separate process in compliance with the requirements of
2L.
Per the approved CSA work plan, ash used in the structural fill was not considered part
of the source area and was not evaluated during the CSA. Based on exceedances from
an area of wetness (AOW) location (S-9) south of the ash basin and west of the
structural fill, monitoring wells GWA-23S and GWA-23D were installed and sampled as
part of the CAMA Round 5 sampling event (April 2016). Exceedances and
concentrations of the constituents in GWA-23S and GWA-23D were similar, indicating
that the concentrations were from the same source.
This comparison of the elevation of the screen in GWA-23S and the ash basin full pond
elevation indicate that the source of the exceedances in GWA-23S is not the ash basin.
Although the bottom of screen elevation for GWA-23D (754.96 to 749.96 feet) is lower
than the former chemical treatment pond area historical elevation (772 feet), based on
the similar nature of the exceedances, it is likely that the same source is the cause of the
exceedances in both GWA-23S and GWA-23D. The approximate elevation for AOW S-9
is 792 feet, which is greater than water elevations in the ash pond and the former
chemical treatment pond.
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The exceedances in GWA 23S/D are consistent with constituents associated with coal
ash and a potential source could be the nearby structural fill. As the structural fill was
constructed under the NCDEQ Division of Waste Management (DWM) structural fill
rules found in 15A NCAC 13B .1700 (Permit No. CCB0070), Duke Energy notified DWM
of these exceedances and an assessment is ongoing at the BCSS structural fill. The
assessment results will be reported to the NCDEQ DWM. See Section 2.7 for a detailed
description of the assessment activities with regards to the structural fill.
Summary of Permitted Activities 2.5
Duke Energy is authorized to discharge wastewater from the BCSS ash basin to the Dan
River (outfall 003). This discharge is in accordance with NPDES Permit NC0024406,
which was renewed on November 1, 2012 and expired on February 28, 2017. A draft
renewal permit (NC0024406) was submitted to NCDEQ on September 9, 2016. BCSS is
currently operating under the expired permit. The renewal permit is proposed to
expire three years after its effective date. As part of the permit renewal, the facility
identified seeps and collected seep samples. The seeps were incorporated into the
permit as outfalls where appropriate. The draft NPDES permit proposes to require
surface water monitoring, including continued sampling of seep outfalls, as part of the
permit conditions.
The current NPDES flow diagram from the permit application for BCSS is provided in
Figure 2-11. Current approximate quantities of inflows into the ash basin include 2.7
million gallons per day (MGD) from the ash sluice, 4.2 MGD from the yard holding
sump, 0.7 MGD from the coal yard sumps, 0.7 MGD from the FGD wastewater
treatment lagoons, 0.46 MGD of stormwater, less than 0.19 MGD from the consolidated
sump system, 0.03 MGD from the chemical holding pond, 0.019 MGD from the west
holding sump. The contributing sources to these inflows are depicted on Figure 2-9.
There are four solid waste facilities associated with BCSS: the active Craig Road Landfill
(NCDEQ Permit No. 8504 - INDUS), the active FGD Landfill (NCDEQ Permit No. 8505 -
INDUS), a closed structural fill (NCDEQ Permit No. CCB0070), and the closed Pine Hall
Road Landfill (NCDEQ Permit No. 8503 - INDUS). The Craig Road Landfill, FDG
Landfill and the structural fill are located south of the ash basin and are not
hydrogeologically connected to the ash basin (although leachate collected from the
landfill facilities are routed to the ash basin). The Pine Hall Road Landfill is located on
the south side of the ash basin and north side of Pine Hall Road and is
hydrogeologically connected to the ash basin (Figure 2-10).
The Pine Hall Road Landfill was closed in December 2008. The landfill was permitted to
accept fly ash from Belews Creek Steam Station operations. The landfill was originally
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permitted in 1983. The original landfill was unlined and was permitted with a soil cap
one foot thick on the side slopes and two feet thick on flatter areas. A subsequent
expansion (Phase I Expansion) was permitted in 2003. This phase was also unlined but
was a synthetic cap system was applied at closure. After groundwater exceedances
were observed in wells installed near the landfill, the placement of additional ash in the
landfill stopped. The closure design was changed to utilize an engineered cover system
for a portion of the landfill. The engineered cover system consists of a 40-mil linear low-
density polyethylene geomembrane, a geonet composite, 18 inches of compacted soil,
and 6 inches of vegetative soil cover. The engineered cover system was installed over a
37.9-acre area. An adjacent 14.5-acre area, located to the northeast, had additional soil
cover applied and was graded to improve surface drainage. The construction of the
engineered cover system and additional soil cover on the 14.5-acre area was completed
in December 2008.
The Craig Road Landfill is permitted to receive CCR and other operational waste
material Phase 1 and 2 of the landfill were constructed with an engineered liner system
consisting of a leachate collection system, underlain by a high-density polyethylene
(HDPE) geomembrane liner, underlain by a geo-synthetic clay liner. The waste
boundary contains an area of approximately 67.1 acres. Phase 1 began accepting waste
in February 2008. Phase 2 began accepting waste in June 2014.
The FGD residue landfill is permitted to receive CCR and other operational waste
material; however Duke only places FGD residue (gypsum) from BCSS operations in
this landfill.
The FGD residue landfill is located south of the Belews Creek plant on land between
two arms of the Belews Reservoir. The West Belews Creek arm of the reservoir is
located west of the landfill site and the East Belews Creek arm of the reservoir is located
east of the site. Craig Road is located to the west of the landfill. The landfill consists of
four cells contained in an area of approximately 24 acres. The adjacent stormwater basin
occupies an area of approximately 2.4 acres and is used to manage leachate and
stormwater collected from the landfill and discharged to the ash basin. The landfill has
an engineered liner system consisting of a leachate collection system, underlain by a
high-density polyethylene (HDPE) geomembrane liner, underlain by a geo-synthetic
clay liner.
The structural fill (see Figure 2-10) comprised of compacted fly ash was constructed
southeast of the ash basin. The structural fill is located south of the Pine Hall Road
topographic divide, and therefore, groundwater flow beneath the fill should be
predominantly away from the ash basin towards Belews Reservoir. This structural fill
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was constructed under the structural fill rules found in 15A NCAC 13B .1700. The
Notification of the Beneficial Use Structural Fill was submitted by Duke Energy to
NCDENR on May 7, 2003. Approximately 968,000 cy of ash were placed within the
structural fill from February 2004 to the last ash placement in July 2009. An engineered
cap similar to that previously described for the Pine Hall Road Landfill was constructed
over the structural fill in 2012. The structural fill is currently used as an
equipment/material staging area and overflow parking. The structural fill was not
considered part of the source area and was not evaluated by the CSA.
History of Site Groundwater Monitoring 2.6
The following sections discuss groundwater monitoring activities conducted association
with the BCSS ash basin. The location of the ash basin voluntary and compliance
monitoring wells, the CSA wells, the approximate ash basin waste boundary, and the
compliance boundary are shown in Figure 2-4. Construction details for site monitoring
wells are provided in Table 2-1. The following sections discuss groundwater
monitoring activities prior to CSA activities through current CAMA assessment
activities.
Ash Basin 2.6.1
Voluntary Groundwater Monitoring
Voluntary monitoring wells MW-101S, MW-101D, MW-102S, MW-102D, MW-
103S, MW-103D, MW-104S, and MW-104D were installed by Duke Energy in
2006 as part of a voluntary monitoring system. The voluntary wells are shown on
Figure 2-10. Duke Energy performed voluntary groundwater monitoring around
the BCSS ash basin from November 2007 until May 2010. During this period, the
voluntary groundwater monitoring wells were sampled biannually and the
analytical results were submitted to NCDENR DWR. Monitoring wells MW-102S
and MW-102D were abandoned as a result of reinforcement construction
activities at the ash basin dam in 2015. Samples have been collected from
monitoring wells MW-103S/D and MW-104S/D since July 2015 as part of
groundwater assessment efforts. No samples are currently being collected from
the other voluntary wells.
NPDES Groundwater Monitoring
Groundwater monitoring as required by BCSS NPDES permit NC0024406 began
in January 2011 as described in NPDES Permit Condition A (10), effective
November 1, 2012. Groundwater monitoring events are conducted three times a
year (January, May, and September). Compliance groundwater monitoring is
continuing in accordance with the draft NPDES permit (NC0024406).
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Locations for the compliance groundwater monitoring wells were approved by
the NCDENR DWR. The compliance groundwater monitoring system for the
BCSS ash basin consists of the following monitoring wells: MW-200S, MW-200D,
MW-201D, MW-202S, MW-202D, MW-203S, MW-203D, MW-204S, and MW-
204D (shown on Figure 2-10 and Table 2-2). All the compliance monitoring wells
were installed in December 2010. The compliance groundwater monitoring is
performed in addition to the normal NPDES monitoring of the discharge flows
from the ash basin.
With the exception of monitoring wells MW-202S and MW-202D, the ash basin
compliance monitoring wells were installed at or near the compliance boundary.
Monitoring wells MW-200S and MW-200D are located to the north of the ash
basin dike. Monitoring well MW-201D is located west of Pine Hall Road near the
former ash basin discharge canal. Monitoring wells MW-203S, MW-203D, MW-
204S, and MW-204D are located west of the ash basin along Middleton Loop
Road.
Landfill Groundwater Monitoring 2.6.2
Groundwater monitoring is conducted at the three permitted BCSS landfills
(Pine Hall Road, Craig Road, and FGD Residue) in accordance with permit
requirements. Monitoring is performed twice per year per an established
schedule at each landfill.
Pine Hall Road Landfill – The groundwater monitoring system currently
consists of 13 monitoring wells and two surface water sample locations.
Twelve wells are screened in the residual soil/saprolite layer and one well
(MW-1D) is screened in fractured bedrock. Groundwater monitoring wells
MW-1, MW-2, MW-3, MW-4, and MW-5 were installed in 1989.
Monitoring well MW-3 was confirmed to monitor background
groundwater quality in CAP 1. The initial twice per year groundwater
sampling was performed at these wells in October 1989.
Monitoring wells MW-6, MW2-7, MW2-9, OB-4, OB-5, and OB-9 were
installed, and monitoring initiated, as part of the site investigation for the
Phase 1 Expansion and subsequent investigation of groundwater
exceedances from 2000 to 2004. Monitoring wells MW-1D and MW-7 were
installed after installation of the engineered cap in 2008. Groundwater
monitoring is performed in April and October per the landfill Water
Quality Monitoring Plan.
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Craig Road Landfill – The groundwater monitoring system currently
consists of 17 monitoring wells, six surface water sample locations and
three leachate sample locations. Monitoring well CRW-10 was confirmed
to monitor background water quality in CAP 1. Monitoring wells were
installed to monitor the transition zone (TZ) between the
saprolite/partially weathered rock zone and bedrock. The initial twice per
year groundwater sampling event was performed in January 2007 prior to
initial placement of waste in February 2008. Groundwater monitoring is
performed in January and July per the landfill Water Quality Monitoring
Plan.
FGD Residue Landfill – The groundwater monitoring system currently
consists of 12 monitoring wells, one surface water sample location and one
leachate sample location. Wells BC-23A and BC-28 were confirmed to
monitor background groundwater quality in CAP 1. The monitoring
wells were installed to monitor groundwater quality in the residual
soil/saprolite layer. The initial twice per year groundwater sampling event
was performed in November 2007 prior to initial waste placement in April
2008. Groundwater monitoring is performed in May and November per
the landfill Water Quality Monitoring Plan.
Ash Basin CAMA Monitoring 2.6.3
One hundred nine (109) groundwater wells were installed as part of this
assessment (Figure 2-10). Eighteen (18) existing voluntary and compliance wells
have been included in assessment activities. Nine background (BG) monitoring
wells BG-1S/D, BG-2S/D/BR/BRA, BG-3S/D and MW-202BR have been installed
to evaluate background water quality in the shallow, deep and bedrock flow
regimes. Two existing background compliance monitoring wells MW-202 S/D,
are also sampled for assessment activities.
Thirty-one (31) groundwater monitoring wells were installed in locations
anticipated to be upgradient of the ash basin: GWA-4S/D, GWA-5S/SA/D/BR2,
GWA-6S/D, GWA-7S/SA/D, GWA-8S/D, GWA-9S/D/BR, GWA-12S/D/BR, GWA-
16S/D/DA/BR, GWA-17S/D, GWA-23S/D, GWA-25BR, GWA-26S/D/BR MW-
201BR and MW-203BR. These groundwater monitoring wells were installed to
evaluate groundwater quality upgradient of the ash basin and to confirm
groundwater flow direction. Eight upgradient voluntary and compliance
monitoring wells are also sampled for assessment activities MW-104S/D/BR,
MW-201D, MW-203S/D, and MW-204S/D.
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Twenty-eight (28) groundwater monitoring wells were installed within the waste
boundary: AB-1S/D/BR, AB-2S/SA/D, AB-3S/D, AB-4S/SL/D/BR/BRD, AB-
5S/SL/D, AB-6S/SL/D, AB-7S/D, AB-8S/SL/D and AB-9S/D/BR/BRD. These
groundwater monitoring wells were installed to evaluate groundwater quality
within the pore water, TZ, upper bedrock, and deeper bedrock zones.
Monitoring wells AB-1S/D/BR, AB-2S/SA/D, and AB-3S/D were installed at the
crest of the ash basin dam. Monitoring wells AB-9S/D/BR/BRD were installed at
the crest of the chemical pond dike. The rest of the monitoring wells within the
waste boundary were installed in the ash basin.
Thirty-nine (39) groundwater monitoring wells were installed outside and
downgradient of the ash basin footprint. The downgradient monitoring wells
include the following: GWA-1S/D/BR, GWA-2S/D, GWA-3S/D, GWA-10S/DA,
GWA-11S/D, GWA-18S/SA/D, GWA-19S/SA/D/BR, GWA-20S/SA/D/BR, GWA-
21S/D, GWA-22S/D, GWA-23S/D, GWA-24S/D/BR, GWA-25BR, GWA-26S/D/BR,
GWA-27S/D/BR, GWA-30S/D, GWA-31S/D, GWA-32S/D and MW-200BR. These
groundwater monitoring wells were installed to evaluate groundwater quality
within the shallow, TZ, and bedrock zones downgradient of the ash basin. Eight
existing downgradient voluntary and compliance monitoring wells
downgradient of the ash basin were also sampled: MW-101S/D, MW-102S/D,
MW-103S/D, and MW-200S/D.
Summary of Assessment Activities 2.7
Ash Basin
With the exception of the voluntary and compliance well groundwater monitoring
described above, no other known groundwater investigations or environmental site
assessments have been conducted at the BCSS ash basin prior to implementation of the
CAMA Groundwater Assessment Work Plan (HDR, 2014).
Solid Waste Facilities
Duke Energy was notified in a letter dated November 9, 2011 from NCDENR Division
of Waste Management (DWM) that exceedances of the 2L Standards were reported in
samples collected from review boundary groundwater monitoring wells at the Pine
Hall Road Landfill which is located to the south and upgradient of the ash basin. HDR
prepared and submitted an assessment to the NCDENR Division of Waste Management
for exceedances of 2L Standards at this landfill (HDR, 2012).
The report assessed 2L Standard exceedances at wells MW-3 and MW-6 and found
those exceedances to be attributed to naturally occurring conditions.
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The assessment report reviewed the location of wells and surface water sample
locations with exceedances of 2L Standards (MW-4, MW-7, MW2-7, MW2-9, SW-1A,
and SW-2) and found that the hydrologic boundaries and the groundwater flow at the
site was such that the groundwater at these locations was flowing to the ash basin. The
report also concluded that with the reduced infiltration, due to the engineered cover
system installed in 2008, the groundwater concentration of constituents attributable to
fly ash in these wells will likely continue to decrease over time.
There have been groundwater assessments associated with the Craig Road Landfill and
FGD Residue Landfill located south of the ash basin on the south side of Belews
Reservoir. There is no hydrogeologic connection between these two landfills and the
ash basin therefore details related to these assessment and their findings are not
included in this report.
Structural Fill
Per the approved CSA work plan, ash used in the structural fill was not considered part
of the source area and was not evaluated during the CSA. Based on exceedances from
AOW S-9 south of the ash basin and west of the structural fill, monitoring wells GWA-
23S and GWA-23D were installed and sampled as part of the CAMA Round 5 sampling
event (April 2016). Exceedances and concentrations of the constituents in GWA-23S
and GWA-23D were similar, indicating that the concentrations were from the same
source.
The exceedances in GWA 23S/D are consistent with constituents associated with coal
ash and a potential source could be the nearby structural fill. As the structural fill was
constructed under the NCDEQ DWM structural fill rules found in 15A NCAC 13B .1700
(Permit No. CCB0070), Duke Energy notified DWM of these exceedances. A Proposed
Groundwater Assessment Monitoring Plan was prepared and submitted to the NCDEQ
DWM in November 2016. The monitoring plan included proposed monitoring well
installation locations, and soil sample and surface water sample locations. The
structural fill assessment is ongoing at BCSS. To date five monitoring wells (SFMW-1D,
SFMW-2D, SFMW-3D, SFMW-4D, and SFMW-5D) have been installed around the
structural fill (Figure 2-10). The monitoring well and surface water samples have been
collected and the results are pending. The results of the structural fill assessment will
be reported to the NCDEQ DWM under separate cover.
Other Site Locations
Between 1991 and 2017, environmental incidents (i.e., releases) occurred at the BCSS site
that initiated notifications to NCDEQ. The historical incidents generally consisted of
releases of motor/lubrication or transformer oil (including illegal dumping by unknown
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parties) that had potential to impact soil and groundwater at the site. A summary of the
historical on-site environmental incidents is provided in Table 2-3.
Summary of Initial Abatement, Source Removal or other 2.8
Corrective Action
A Settlement Agreement between NCDEQ and Duke Energy signed on September 29,
2015, requires accelerated remediation to be implemented at sites that demonstrate off-
site groundwater impacts. Historical and 2015 CSA assessment information indicates
the potential for off-site groundwater impact northwest of the BCSS ash basin in the
area of the 2.23-acre parcel (hereafter Parcel A) not owned by Duke Energy.
Constituents associated with coal ash pore water have been identified within
groundwater in shallow (saprolite) and deep (transition zone between saprolite and
competent bedrock) flow layers between the ash basin and Parcel A and downgradient
of Parcel A. Groundwater in shallow and deep layers near Parcel A flows north and
northwest toward the Dan River (located approximately 2,500 feet downstream of
parcel A). Groundwater monitoring wells delineating concentrations in this area are
located on Duke Energy property. The compliance boundary coincides with the
southeast property line of Parcel A.
Duke Energy provided an Accelerated Remediation Summary report to NCDEQ on
February 17, 2016 which supplemented and updated information included with the
CAP Part 2. In correspondence dated March 28, 2016, NCDEQ acknowledged receipt of
the Remediation Summary and requested additional information. NCDEQ
conditionally approved the Interim Action Plan (IAP) in a letter dated July 22, 2016 with
the condition (among others) that a Basis of Design (BOD) Report be submitted for
review. Duke Energy provided a response to the conditional approval letter on
September 9, 2016. In follow-up, the Table of Contents for the Basis of Design report
was adjusted by NCDEQ in a letter dated September 27, 2016.
Interim action activities associated with Parcel A consisted of pilot testing with the
potential of installing a groundwater extraction system along the northwest corner of
the ash basin. Specific objectives outlined in the Interim Action Plan (HDR, 2016) were:
Acquire Parcel A. This activity is no longer being pursued by Duke Energy.
Conduct initial aquifer tests to evaluate feasibility and aid in the preliminary
design of a groundwater extraction system and/or subsurface barrier wall.
Recently completed aquifer tests indicate groundwater extraction is a viable
remedial alternative at BCSS.
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Initiate preliminary design of a groundwater extraction system.
Initiate permitting for a groundwater extraction system.
Implementation of a groundwater extraction system located between the ash basin and
the southeast side of Parcel A will reduce groundwater flow from the ash basin prior to
migration toward Parcel A. The primary objective of the groundwater extraction
system is to reduce groundwater migration of source area constituents from the ash
basin towards the 2.23-acre parcel and achieve a hydraulic boundary proximal to the
extraction well network.
The following BOD reports have been submitted to date. The purpose of the BOD
reports are to provide a system layout and sizing of system components including
wells, piping, pumps, discharge system with control system capabilities and power
requirements. A 30 % BOD report was submitted to NCDEQ on December 21, 2016 and
review comments were received on February 1, 2017. A 60% BOD report was submitted
on April 10, 2017 and review comments were received on June 30, 2017. The 100% BOD
report was submitted to NCDEQ DWR on September 1, 2017.
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3.0 SOURCE CHARACTERISTICS
For purposes of this assessment, the source area is defined by the ash waste boundary
as depicted on Figure 2-1. For the BCSS site, sources include the ash basin, Pine Hall
Road Landfill, and the former chemical pond.
Coal Combustion and Ash Handling System 3.1
Coal ash is produced from the combustion of coal. The coal is dried, pulverized, and
conveyed to the burner area of a boiler. The smaller particles produced by coal
combustion, referred to as fly ash, are carried upward in the flue gas and are captured
by an air pollution control device, such as an electrostatic precipitator. The larger
particles of ash that fall to the bottom of the boiler are referred to as bottom ash.
BCSS historically produced approximately 650,000 tons of ash per year although in
recent years, this number has decreased to approximately 450,000 tons per year. Note
that these quantities are an estimate based on generation rates, outages, coal
mineralogy, and other factors.
Coal ash residue from the coal combustion process has historically been disposed of in
the ash basin. Prior to 1984, fly ash and bottom ash generated at the station was sluiced
to the ash basin. The Pine Hall Road Landfill was permitted in 1983 when the station
converted to dry handling of fly ash. Fly ash is still occasionally sluiced to the ash basin
during startup or maintenance activities.
Ash Basin
The station’s ash basin consists of a single cell impounded by two earthen dams located
on the north end of the ash basin and an embankment dam located in the northeast
portion of the basin along Pine Hall Rd. The main dam is approximately 2,000 feet long
and a maximum of approximately 140 feet high. The top of the dam is at elevation 770
feet and the crest is 20 feet wide. The ash basin was constructed from 1970 to 1972 and is
located approximately 3,200 feet northwest of the BCSS powerhouse. The area
contained within the ash basin waste boundary is approximately 283 acres (shown on
Figure 2-1).
The normal operating elevation of the BCSS ash basin pond is 750 feet, while full pond
elevation is approximately 768.2 feet. The full pond capacity of the ash basin is
estimated to be 17,656,000 cubic yards (cy).
The ash basin is operated as an integral part of the station’s wastewater treatment
system, which receives flows from the ash removal system, BCSS powerhouse and yard
sumps, coal yard sumps, stormwater, landfill leachate, and treated FGD wastewater.
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During station operations, inflows to the ash basin are highly variable due to the
cyclical nature of station operations. Inflows from the station to the ash basin are
discharged into the southeast portion of the ash basin.
The discharge from the ash basin is through a concrete discharge tower located in the
northwest portion of the ash basin. The concrete discharge tower drains through a 21-
inch-inside diameter high-density polyethylene (HDPE) conduit for approximately
1,600 feet and then discharges into a concrete flume box. The ash basin pond elevation
is controlled by the use of concrete stop logs in the discharge tower. The discharge is to
the designated effluent channel that flows northwest to the Dan River. The discharge
from the ash basin is permitted by the NCDEQ DWR under NPDES Permit NC0024406.
The ash basin originally discharged to Belews Reservoir through a concrete discharge
tower located at the east end of the ash basin. Due to water quality issues in Belews
Reservoir, in 1984 the original discharge was closed current discharge tower was
constructed. The original discharge tower was filled with flowable fill in the mid 1990’s.
Duke Energy permanently closed the original discharge tower with cementitious grout
in 2015 to avoid potential inadvertent discharges to Belews Reservoir.
Pine Hall Road Landfill
The Pine Hall Road Landfill (NCDENR Permit No. 8503 - INDUS) received a permit to
operate on December 10, 1984 and a subsequent expansion (Phase I Expansion) was
permitted in 2003. The unlined landfill was permitted to receive fly ash from the
combustion of coal at BCSS. The total footprint of the landfill is approximately 67.2
acres. A total of approximately 8,500,000 cubic yards (cy) of ash was placed within the
Pine Hall Road Landfill between December 1984 and March 2008.
Structural Fill
An unlined structural fill comprised of compacted fly ash was constructed southeast of
the ash basin. The structural fill is located south of the Pine Hall Road topographic
divide and, therefore, groundwater flow beneath the fill should be predominantly away
from the ash basin towards Belews Reservoir. The structural fill is not considered part
of the source area evaluated by this CSA.
Approximately 968,000 cy of ash were placed within the structural fill.
General Physical and Chemical Properties of Ash 3.2
Coal ash consists of fly ash and bottom ash produced from the combustion of coal. The
physical and chemical properties of coal ash are determined by reactions that occur
during the combustion of the coal and subsequent cooling of the flue gas.
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Physical Properties
Approximately 70 to 80 percent of the ash produced during coal combustion is fly ash
(EPRI, January 1995). Typically 65 to 90 percent of fly ash has particle sizes that are less
than 0.010 millimeter (mm). In general, fly ash has a grain size distribution similar to
that of silt. The remaining 20 to 30 percent of ash produced is considered to be bottom
ash. Bottom ash consists of angular particles with a porous surface and is normally gray
to black in color. Bottom ash particle diameters can vary from approximately 38 to 0.05
mm. In general, bottom ash has a grain size distribution similar to that of fine gravel to
medium sand (EPRI, January 1995).
Based on published literature not specific to the BCSS site, the specific gravity of fly ash
typically ranges from 2.1 to 2.9, and the specific gravity of bottom ash typically ranges
from 2.3 to 3.0. The permeability of fly ash and bottom ash vary based on material
density, but would be within the range of a sand-gravel with a similar gradation, grain
size distribution, and density (EPRI, January 1995).
Chemical Properties
In general, the specific mineralogy of coal ash varies based on many factors including
the chemical composition of the coal, which is directly related to the geographic region
where the coal was mined, the type of boiler where the combustion occurs (i.e.,
thermodynamics of the boiler), and air pollution control technologies employed.
The overall chemical composition of coal ash resembles that of siliceous rocks from
which it was derived, particularly shale. Oxides of silicon, aluminum, iron, and calcium
make up more than 90 percent of most siliceous rocks, soils, fly ash, and bottom ash.
Other major and minor elements (sulfur, sodium, potassium, magnesium, titanium)
make up an additional 8 percent, while trace constituents account for less than 1
percent. The following constituents are considered to be trace elements: arsenic, barium,
cadmium, chromium, lead, mercury, selenium, copper, manganese, nickel, lead,
vanadium, and zinc (EPRI, 2010). The historical specific coal sources used at BCSS are
bituminous coal from Northern Appalachia and Central Appalachia.
The majority of fly ash particles are glassy spheres mainly composed of amorphous or
glassy aluminosilicates, crystalline matter, and carbon. Figure 3-1 presents a
photograph of ash collected from the ash basin at Duke Energy’s Cliffside Steam Station
(which is considered representative of the ash at BCSS) showing a mix of fly ash and
bottom ash at 10 µm and 20 µm magnifications. The glassy spheres can be observed in
the photograph. The glassy spheres are generally resistant to dissolution. During the
later stages of the combustion process, and as the combustion gases are cooling after
exiting the boiler, molecules from the combustion process condense on the surface of
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the glassy spheres. These surface condensates consist of soluble salts (e.g. calcium
(Ca2+), sulfate (SO42-), metals (copper (Cu), zinc (Zn)), and other minor elements (e.g.
boron (B), selenium (Se), and arsenic (As)) (EPRI 1995).
The major elemental composition of fly ash (approximately 95 percent by weight) is
composed of mineral oxides of silicon, aluminum, iron, calcium. Oxides of magnesium,
potassium, titanium and sulfur comprise approximately 4 percent by weight (EPRI,
January 1995). Trace elemental composition typically is approximately 1 percent by
weight and may include arsenic, antimony, barium, boron, cadmium, chromium,
copper, manganese, mercury, nickel, lead, selenium, silver, thallium, zinc, and other
elements. For comparison, Figure 3-2 shows the elemental composition of fly ash and
bottom ash compared with typical values for shale and volcanic ash. Table 3-1 shows
the bulk composition of fly ash and bottom ash compared with typical values for soil
and rock. In addition to these constituents, fly ash may contain unburned carbon.
Bituminous coal ash typically yields slightly acidic to alkaline solutions with pH levels
ranging from approximately 5 to 10 on contact with water.
The geochemical factors controlling the reactions associated with leaching of ash are
complex. Factors such as the chemical speciation of the constituent, solution pH,
solution-to-solid ratio, and other factors control the chemical concentration of the
resultant solution. Constituents that are held on the glassy surfaces of fly ash such as
boron, arsenic, and selenium may initially leach more readily than other constituents.
As noted in Table 3-1, aluminum, silicon, calcium, and iron represent the larger
fractions of fly ash by weight. Calcium and iron may limit the release of arsenic by
forming calcium-arsenic precipitates. Formation of iron hydroxide compounds may also
sequester arsenic and retard or prevent release of arsenic to the environment. Similar
processes and reactions may affect other constituents of concern; however, certain
constituents such as boron and sulfate will likely remain highly mobile.
In addition to the variability that might be seen in the mineralogical composition of the
ash, based on different coal types, different age of ash in the basin, etc., it is anticipated
that the chemical environment of the ash basin varies over time, distance, and depth.
EPRI (EPRI, 2010) reports that 64 samples of coal combustion products (including fly
ash, bottom ash, and FGD residue) from 50 different power plants were subjected to
EPA Method 1311 Toxicity Characteristic Leaching Procedure (TCLP) leaching and no
TCLP result exceeded the TCLP hazardous waste limit. Figure 3-3 provides the results
of that testing.
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Site-Specific Coal Ash Data 3.3
Source characterization was performed to identify the physical and chemical properties
of the ash in the source areas. The source characterization involved developing selected
physical properties of ash, identifying the constituents found in ash, measuring
concentrations of constituents present in the ash pore water, and performing laboratory
analyses to estimate constituent concentrations resulting from the leaching process. The
physical and chemical properties evaluated as part of this characterization will be used
to better understand impacts to soil and groundwater from the source area and will also
be utilized as part of groundwater model development in the CAP.
Source characterization was performed through the completion of soil borings,
installation of monitoring wells, and collection and analysis of associated solid matrix
and aqueous samples. Ash samples were collected for analysis of physical
characteristics (e.g., grain size, porosity, etc.) to provide data for evaluation of
retention/transport properties within and beneath the ash basin. Ash samples were
collected for analysis of chemical characteristics (e.g., total inorganics, leaching
potential, etc.) to provide data for evaluation of constituent concentrations and
distribution. Samples were collected in general accordance with the Work Plan.
Groundwater monitoring wells were installed inside the waste boundary of the ash
basin as part of the 2015 CSA investigation. In the boring and monitoring wells
performed within the Ash Basin ash was encountered at varying intervals, from 18 to 66
feet below ground surface; auger refusal was encountered between approximately 68 to
88 feet below ground surface (bgs) indicating competent rock. Water levels ranged from
approximately 3.4 to 7.6 feet bgs, causing ash to be saturated. Ash was not observed in
borings outside the ash basin. Laboratory results of ash samples are presented in
Appendix B, Table 4.
Physical Properties of Ash
Physical properties (grain size, specific gravity, and moisture content) were performed
on seven fly ash samples from the ash basin. Physical properties were measured using
ASTM methods, lab reports are provided in Appendix C. Ash is generally
characterized as a non-plastic silty (medium to fine) sand or silt. Compared to soil, fly
ash exhibits a lower specific gravity with two values reported from AB-6GTB (1.7) and
AB-7SL (2.2). Moisture content of the fly ash samples ranges from 11.2 to 65.4% (Table
3-2). Ash was generally described as gray to dark gray, non-plastic, loose to medium
density, dry to wet, fine- to coarse-grained sandy silt texture.
Chemical Properties of Ash
Ash samples were collected during the installation of the monitoring wells inside the
waste boundary of the ash basin as part of the 2015 CSA investigation. Concentrations
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of arsenic, boron, chromium, cobalt, iron, manganese, selenium, and vanadium were
reported above soil background concentrations and the North Carolina Preliminary Soil
Remediation Goals (PSRGs) for Industrial Health and/or Protection of Groundwater for
ash samples collected within the ash basin waste boundary (Appendix B, Table 4).
In addition to total inorganic testing of ash samples, seven ash samples collected from
borings completed within the ash basin were analyzed for leachable inorganics using
Synthetic Precipitation Leaching Procedures (SPLP) (Appendix B, Table 6). The
purpose of the SPLP testing is to evaluate the leaching potential of constituents that
may result in impacts to groundwater above the 2L Standards or IMACs. The results of
the SPLP analyses indicated that antimony, arsenic, chromium, cobalt, iron, manganese,
selenium, thallium, and vanadium exceeded their respective 2L Standard or IMAC.
Although SPLP analytical results are being compared to the 2L Standards or IMAC,
these samples do not represent groundwater samples and the 2L Standards and IMACs
are not applicable to the results (presented for comparative purposes only).
Background soil SPLP data collected from various sites in the Piedmont is presented as
Table 3-3. The following metals leach from naturally occurring soils in similar geologic
settings at concentrations greater than 2L or IMAC: barium, chromium, cobalt, iron,
manganese, nickel, thallium, and vanadium.
Chemistry of Ash Pore water
Pore water refers to water samples collected from wells installed within the ash basins
and screened in the ash layer. Nine pore water monitoring wells (AB-4S, AB-4SL, AB-
5S, AB-5SL, AB-6S, AB-6SL, AB-7S, AB-8S, and AB-8SL) were installed within the ash
basin waste boundary and were screened within the ash layer. Since installation as part
of the first 2015 CSA, these wells have been sampled eight times up to the second
quarter of 2017 as part of the CAMA monitoring program.
Concentrations of antimony, arsenic, beryllium, boron, chloride, chromium, cobalt, iron,
manganese, selenium, sulfate, thallium, vanadium, and total dissolved solids (TDS)
have been reported above the background groundwater concentration range and 2L
Standards or IMACs in pore water samples collected from wells within the ash basin.
The pore water sampling results show a decrease in constituent concentrations at some
locations with most locations showing stable concentrations. No significant increases in
constituent concentrations were observed. Pore water sample locations and results are
shown on Figure 2-10 and are listed in (Appendix B, Table 1). Piper diagrams have
been prepared for groundwater results from BCSS monitoring wells and are discussed
in Section 10.0.
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Relative redox conditions were determined using an assignment of redox conditions
based on concentrations of dissolved oxygen (O2), nitrate (NO3–), manganese (Mn2+),
iron (Fe2+), sulfate (SO42–), and sulfide (sum of dihydrogen sulfide [aqueous H2S],
hydrogen sulfide [HS–], and sulfide [S2–])for identifying redox processes in groundwater
(Jurgens, McMahon, Chapelle, & Eberts, 2009). This workbook allows a standardized
method to identify and describe the redox state of groundwater. The ash pore water is
generally anoxic to mixed (oxic-anoxic).
Ash pore water at BCSS for AB-4S, AB-7S, and AB-8S resembles bituminous coal ash
leachate water from EPRI’s 2006 study which is a calcium-magnesium-sulfate water
type. In comparison, BCSS ash pore water from AB-6S and AB-8SL have an elevated
bicarbonate component.
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4.0 RECEPTOR INFORMATION
Section §130A-309.201(13) of the CAMA defines receptor as “any human, plant, animal, or
structure which is, or has the potential to be, affected by the release or migration of
contaminants. Any well constructed for the purpose of monitoring groundwater and
contaminant concentrations shall not be considered a receptor.” In accordance with the
NORR CSA guidance, receptors cited in this section refer to public and private water
supply wells (including irrigation wells and unused wells) and surface water features.
Refer to Section 12.0 for a discussion of ecological receptors.
The NORR CSA receptor survey guidance requirements include listing and depicting
all water supply wells, public or private, including irrigation wells and unused wells
unless such wells have been properly abandoned in accordance with 15A NCAC 2C
.0113, within a minimum of 1,500 feet of the known extent of contamination. In
NCDEQ’s June 2015 response to Duke Energy’s proposed adjustments to the CSA
guidelines, NCDEQ DWR acknowledged the difficulty with determining the known
extent of contamination at this time and stated that they expected all drinking water
wells located 2,640 feet (0.5-mile) downgradient from the established compliance
boundary to be documented in the CSA reports as specified in the CAMA requirements.
Water supply well locations near BCSS are depicted on the USGS map (Figure 4-1). The
approach to the receptor survey in this CSA includes listing and depicting all water
supply wells (public or private, including irrigation wells and unused wells) within a
0.5-mile radius of the ash basin compliance boundary (Table 4-1).
Properties located within the 0.5-mile radius of the BCSS ash basin compliance
boundary generally consist of residential properties located to the southwest and
residential farm land northeast, north, and west. Duke Energy property is located to the
north, northwest, south, and east with Belews Reservoir beyond to the south and east
(Figure 4-2).
No residential potable water supply lines are available to the area, with the nearest
residential water supply line, provided by the Town of Walnut Cove, located at the
intersection of Martin-Luther King Jr. Road and Crestview Drive, approximately 4.5
miles to the west from the Duke Power Steam Plant Road entrance to the Station. BCSS
plant is supplied with potable water from the City of Winston-Salem. The water line
enters the property from the south along Craig Road and does not extend beyond that
location.
NORR CSA guidance requires that subsurface utilities are to be mapped within 1,500
feet of the known extent of contamination in order to evaluate the potential for
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preferential pathways. Identification of piping near and around the ash basin was
conducted by Stantec in 2014 and 2015 and utilities around the Site were also included
on a 2015 topographic map by WSP USA, Inc. (Appendix E). It is anticipated that any
underground utilities present at the site would not act as potential preferential
pathways for contaminant migration through underground utility corridors to water
supply well receptors. The flow of groundwater from the ash basin is north toward the
Dan River.
Summary of Receptor Survey Activities 4.1
Surveys to identify potential receptors for groundwater including public and private
water supply wells (including irrigation wells and unused or abandoned wells) and
surface water features within a 0.5-mile radius of the Site compliance boundary have
been reported to NCDEQ:
Drinking Water Well and Receptor Survey – Belews Creek Steam Station (HDR, 2014),
Supplement to Drinking Water Well and Receptor Survey – Belews Creek Steam Station
(HDR, 2014),
Comprehensive Site Assessment Report – Belews Creek Steam Station Ash Basin, (HDR,
2015a),
Drinking Water Well and Receptor Survey – Belews Creek Steam Station (HDR, 2014).
The first report submitted in September 2014 (Drinking water Well and Receptor Survey,
HDR) included the results of a review of publicly available data from NCDEQ, NC
OneMap GeoSpatial Portal, DWR Source Water Assessment Program (SWAP) online
database, county Geographic Information System (GIS), Environmental Data Resources,
Inc. (EDR) Records Review, the United States Geological Survey (USGS) National
Hydrography Dataset, as well as a vehicular survey along public roads located within
0.5 mile radius of the compliance boundary (Appendix D).
The second report submitted in November 2014 (Supplement to Drinking Water Well and
Receptor Survey, HDR) supplemented the initial report with additional information
obtained from questionnaires completed by property owners who own property within
the 0.5 mile radius of the compliance boundary(Appendix D). The report included a
sufficiently scaled map showing the coal ash facility location, the boundary of the Site,
the waste and compliance boundaries, all monitoring wells listed in the NPDES permit
and the approximate location of identified water supply wells. Table 4-2 presents
available information about identified wells including the owner's name, address of the
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well with parcel number, construction and usage data, and the approximate distance
from the compliance boundary.
The questionnaires were designed to collect information regarding whether a water
well or spring is present on the property, its use, and whether the property is serviced
by a municipal water supply. If a well is present, the property owner was asked to
provide information regarding the well location and construction information. The
results from the previous survey and the questionnaires indicated approximately 51
wells might be located within or in close proximity to the survey area (public wells,
assumed private wells, field identified private wells, and recorded private wells).
Summary of Receptor Survey Findings 4.2
No public or private drinking water wells or wellhead protection areas were found to
be located downgradient of the ash basin. This finding was supported by field
observations, a review of public records and groundwater flow direction. The location
and relevant information pertaining to suspected water wells located upgradient or
sidegradient of the facility, within 0.5 miles of the compliance boundary, were included
in the survey reports as required by the NORR.
As required by G.S. 130A-309.211(c1) of House Bill 630 (HB630), Duke Energy evaluated
the feasibility and costs of providing a permanent replacement water supply to eligible
households. Households were eligible if any portion of a parcel of land crossed the 0.5
mile compliance line described in House Bill 630 and if the household currently used
well water or bottled water (under Duke Energy’s bottled water program) as the
drinking water source. Undeveloped parcels were identified but were not considered
“eligible” because groundwater wells are not currently utilized as a drinking source. A
Potable Water Programmatic Evaluation (Dewberry, November 2016; Appendix E) was
conducted and consisted of a survey of eligible households and a preliminary
engineering evaluation, cost estimate and schedule. The evaluation report included a
listing and relevant information for households/properties within the survey area and
maps depicting property locations including those properties for which a replacement
water supply will be provided. Base on the report, 19 of the 58 households surrounding
BCSS have been recommended for installation of an individual filtration system.
A total of 51 water supply wells were identified within a 0.5-mile radius of the
ash basin compliance boundary.
Thirty-nine (39) private water supply wells were identified within a 0.5-mile
radius of the ash basin compliance boundary. The Stokes County Department,
Division of Environmental Health had records for 20 of the 39 private water
supply wells.
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Eleven additional private water supply wells are assumed at residences located
within a 0.5-mile radius of the ash basin compliance boundary, based on the lack
of public water supply in the area and proximity to other residences that have
private wells.
One public water supply well was identified within a 0.5-mile radius of the ash
basin compliance boundary.
No wellhead protection areas were identified within a 0.5-mile radius of the ash
basin compliance boundary.
Several surface water bodies that flow from the topographic divide along
Middleton Loop Road toward the Dan River were identified within a 0.5-mile
radius of the ash basin.
Public Water Supply Wells 4.2.1
One public supply well was located during the receptor survey within 0.5-mile
radius of the ash basin compliance boundary. The Withers Chapel United
Methodist Church (UMC) public water supply well is approximately 1,750 feet
(0.3 miles) northeast of the ash basin.
Private Water Supply Wells 4.2.2
A total of 50 private water supply wells were identified within the 0.5-mile
radius of the ash basin compliance boundary; most northeast of the ash basin
along Pine Hall Road and Middleton Loop, and west and southwest of the ash
basin along Middleton Loop, Old Plantation Road, Pine Hall Road, and Martin
Luther King Jr. Road.
Several efforts have been made to locate and document the presence of and
information related to private water supply wells in the vicinity of BCSS. Duke
Energy submitted a Drinking Water Well and Receptor Survey report in September
2014, and subsequently submitted a supplement to the receptor survey in
November 2014. The November 2014 report supplemented the initial report with
information obtained from questionnaires sent to owners of property within the
0.5-mile radius of the compliance boundary. The questionnaires were designed
to collect information regarding whether a water well or spring is present on the
property, its use, and whether the property is serviced by a municipal water
supply. If a well is present, the property owner was asked to provide
information regarding the well location and construction information. The
results from the receptor surveys and the questionnaires indicated that one
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public water supply wells and 50 private water supply wells were in use within
0.5 miles of the BCSS ash basin compliance boundary.
The receptor survey reports included a sufficiently scaled map showing the ash
basin location, the facility property boundary, the waste and compliance
boundaries, all monitoring wells, and the approximate location of identified
water supply wells. A table presented available information related to identified
wells, including: the owner's name, the address of the well location with parcel
number, construction and usage data, and the approximate distance of the well
from the compliance boundary.
Private and Public Well Water Sampling 4.3
Between February and July 2015, NCDEQ arranged for independent analytical
laboratories to collect and analyze water samples obtained from private wells identified
during the Well Survey, if the owner agreed to have their well sampled.
At the time of the 2015 CSA report, NCDEQ had collected and analyzed a total of 7
groundwater samples from 7 private water supply wells within a 0.5 mile radius of the
BCSS ash basin compliance boundary. The analytical data was provided in the 2015
CSA report as an appendix.
NCDEQ continued to collect and analyze samples from water supply wells within a 0.5
mile radius of the BCSS ash basin compliance boundary during 2015 and early 2016. A
total of 36 samples from 36 private monitoring wells were collected by NCDEQ.
Duke Energy collected samples from private water supply wells in 2016 and 2017 after
the NCDEQ sampling effort. Sample IDs in the 1000 and 2000 range were sampled by
Duke Energy.
Table 4-3 provides tabulated results, provided by Duke Energy, for the NCDENR and
Duke Energy sampling results as well as identified exceedances of 2L Standards,
IMACs, and/or other regulatory limits. For many of the wells sampled in this program,
as with standard practice, samples were split for analysis by Duke Energy’s certified
(North Carolina Laboratory Certification #248) laboratory. The results were judged by
Duke Energy to be substantially the same as the NCDENR results; however the analysis
of determining potential groundwater impact focuses on NCDENR results.
A review of the analytical data for the water supply wells indicated several constituents
were detected above 2L or IMACs including pH (19 wells), arsenic (six wells),
chromium (one well), cobalt (one well), iron (five wells), manganese (six wells), and
vanadium (ten wells). Concentrations of analyzed constituents exceeded their
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respective bedrock provisional background threshold values (PBTVs) for a number of
private water supply wells (data/values biased by the presence of high turbidity are
excluded) including:
Arsenic – 23 wells Barium – 18 wells
Beryllium – 1 well Cadmium – 4 wells
Calcium – 25 wells Chromium (hexavalent) – 8 wells
Chromium (total) – 1 well Copper – 19 wells
Iron – 10 wells Lead – 36 wells
Magnesium – 20 wells Manganese – 14 wells
Molybdenum – 7 wells Nickel – 1 well
Selenium – 2 wells Sodium – 1 well
Sulfate – 9 wells TDS – 10 wells
Vanadium – 10 wells Zinc – 25 wells
The exceedances of PBTVs in private water wells was further evaluated. First, the
bedrock PBTVs have been developed using groundwater data from two background
bedrock wells located on the BCSS site. The geochemical data from these wells may not
be representative across the broader area encompassed by the private water supply
wells surrounding the site. Second, well construction may influence analytical results.
For example, galvanized pipe could yield high zinc concentrations. Information
concerning well construction and piping materials is important to have before
attributing detections of metals solely to the geochemistry of the groundwater. Third, as
described, private water wells in bedrock are typically installed as open-hole wells.
Care must be taken when comparing geochemical data from these wells and comparing
them to background concentrations derived from carefully drilled and installed
groundwater monitoring wells with machine-slotted well screens, proper filter pack
installation, proper well development, and proper sample collection procedures
employed. Fourth, there is very limited information available about the wells (e.g., date
of installation, drilling method, well depth, casing length, pump set depth, etc.). Many
private water supply wells in this part of the Piedmont are open-hole rock wells. A
shallow surface casing is installed and then the well is drilled to a depth that may be as
shallow as 40 or 50 feet or as deep as several hundred feet. When a groundwater sample
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is collected, it is unknown from what part of the bedrock aquifer the groundwater is
drawn. Groundwater geochemistry in fractured bedrock aquifers can be quite variable.
Based on the bedrock groundwater flow direction at the site (Figures 6-10 and 6-11,
discussed in Section 6.3) private water supply wells located west of the ash basin along
Old Plantation Road (WSWs samples BC2019-RAW, BC2 Well 1, BC2 Well 2, BC-1007,
BC4, BC4A and BC4B) are located sidegradient and in relative proximity to the ash
basin. The remaining water supply wells identified in the area are located upgradient
or sidegradient substantially beyond the expected flow zone of the BCSS ash basin.
Analytical data is not available for water supply well BC4. The turbidity reading in BC4
Well B at the time of sampling was 19.3 NTU, therefore the data is not considered valid,
and is not evaluated.
Iron was reported at concentrations which exceed the bedrock PBTV (228 µg/L) and the
2L standard (300 µg/L) in water supply well samples BC-1007, BC2 Well 1, BC2 Well 2,
and BC2019-RAW. However, the iron concentrations in these water supply wells are
within the background concentration range for similar Piedmont geologic settings
(Table 4-4).
Vanadium was reported at a concentration greater than the IMAC but less than the
bedrock PBTV in water supply well sample BC2019-RAW, and greater than the IMAC
and PBTV in BC4 Well A. However, the vanadium concentrations in these water
supply wells are within the background concentration range for similar Piedmont
geologic settings (Table 4-4).
Boron was not detected in any of these water supply wells sampled sidegradient of the
ash basin along Old Plantation Road.
A Piper diagram for water supply well data compared to ash basin pore water,
background bedrock monitoring wells and bedrock monitoring wells located
downgradient of the ash basin (between the ash basin and the private water supply
wells) is presented as Figure 4-3. Observations based on the diagram include:
Water supply wells are characterized as calcium bicarbonate water type,
consistent with samples collected from the background bedrock well at BCSS.
Monitoring well MW-203BR (located between the ash basin and the private
water supply wells to the west) plots along with background well BG-2BR,
indicating this well is likely representative of unimpacted groundwater.
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Monitoring well GWA-9BR (located between the ash basin and the private water
supply wells to the west) plots between calcium-magnesium sulfate type water
and calcium bicarbonate water, a result of the concentration of chloride (52.7
mg/L) relative to the concentration of sulfate and may indicate potential mixing
with source area groundwater.
A more thorough evaluation of piper diagrams related to ash pore water, downgradient
groundwater, and background conditions is provided in Section 10 of this report. The
water quality signature of the water supply wells is similar to the background bedrock
well data at the site indicating that these wells reflect natural background conditions.
See Section 10.1 for background concentrations determined through statistical analysis.
Numerical Well Capture Zone Analysis 4.4
In BCSS CAP 2 (HDR, 2016d), potential constituent of interest (COI) impacts to private
water supply wells located within the model domain were evaluated through particle
tracking simulations by applying a constant pumping rate of 400 gallons per day in
each well, which represents the average household usage per United States
Environmental Protection Agency (USEPA) Water Sense Partnership Program (USEPA,
2015). Reverse particle tracking was conducted for private water supply wells within
the model domain. The reverse particle tracks did not reach the BCSS Compliance
Boundary, indicating the water supply wells located beyond the compliance boundary
did not have ash-related impacts (Figure 4-2).
Surface Water Receptors 4.5
The Site is located in the Roanoke River watershed. The site is located between Belews
Reservoir to the south and the Dan River to the north. Groundwater influenced by the
ash basin flows north toward to the ash basin designated effluent channel that extends
from the base of the ash basin dam and flows northwards through Duke Energy
property discharging to the Dan River (NPDES outfall 003). Surface water classifications
in North Carolina are defined in 02B. 0101 (c). The surface water classification for the
Dan River and Belews Reservoir in the vicinity of the BCSS site is Class WS-IV and
Class WS-IV–C, respectively. Class WS-IV waters are protected as water supplies which
are generally in moderately to highly developed watersheds. Class C are waters
protected for uses such as secondary recreation, fishing, wildlife, fish consumption,
aquatic life including propagation, and survival.
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No surface water intakes, other than the intake used to pump water from Belews
Reservoir for BCSS plant operations, the intake on Belews Reservoir to pump water for
water trucks at the Craig Road Landfill, and the backup intake for cooling lake makeup
water on the Dan River, are located in the vicinity of BCSS either in Belews Reservoir or
in the Dan River.
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5.0 REGIONAL GEOLOGY AND HYDROGEOLOGY
North Carolina lies within three physiographic provinces of the southeastern United
States: the Coastal Plain, Piedmont, and Blue Ridge (Fenneman, 1938). The BCSS site is
located in the Piedmont province. The Piedmont province is bounded to the east and
southeast by the Atlantic Coastal Plain and to the west by the escarpment of the Blue
Ridge Mountains, with a width ranging from 150 miles to 225 miles in the Carolinas
(LeGrand, 2004). A discussion of geology and hydrogeology relevant to the BCSS site is
provided below.
Regional Geology 5.1
The topography of the Piedmont region is characterized by low, rounded hills and long,
rolling, northeast-southwest trending ridges (Heath R. C., 1984). Stream valley to ridge
relief in most areas ranges from 75 feet to 200 feet. Along the Coastal Plain boundary,
the Piedmont region rises from an elevation of 300 feet above mean sea level, to the base
of the Blue Ridge Mountains at an elevation of 1,500 feet (LeGrand, 2004), (Daniel &
Dahlen, 2002).
The BCSS site is within the Milton terrane, one of a number of tectonostratigraphic
terranes that have been defined in the southern and central Appalachians. It is bounded
on the northwest by the Dan River Basin and Sauratown Mountains Anitclinorium and
on the southeast by the Carolina terrane of the larger Carolina superterrane (Figure 5-1;
(Horton, Jr., Drake, Jr., & Rankin, 1989); (Hibbard, Stoddard, Secor, & Dennis, 2002);
(Hatcher, Jr., Bream, & Merschat, 2007)). A geologic map of the area around the BCSS
site is provided as Figure 5-2.
The Milton terrane is characterized by strongly foliated gneisses and schists, commonly
with distinct compositional layering and felsic composition; quartzite, calc-silicate
gneiss, and marble are minor units (Carpenter III, 1982); (Butler & Secor, 1991). The
available evidence suggest that the rocks of the Milton terrane are mainly Precambrian
in age and were metamorphosed and deformed during the early to late Paleozoic
(Butler & Secor, 1991)). The majority of the rocks in the belt are metamorphosed to the
sillimanite and kyanite grade of amphibolite metamorphism (Butler & Secor, 1991). A
steep metamorphic gradient occurs along the southeastern boundary where the grade
decreases to the chlorite zone of greenschist metamorphism in the adjacent Carolina
terrane (Butler & Secor, 1991). This boundary with the Carolina terrane is also a
lithologic discontinuity and is marked locally with sheared rocks (Carpenter III, 1982).
The southwestern boundary of the belt is placed where the gneiss and schist units give
way to the dominant non-layered mafic and felsic intrusive rocks of the Charlotte
terrane (Butler J. R., 1980).
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The Dan River Triassic Basin (Danville Basin in Virginia) is one of several exposed rift
basins that form two parallel belts that strike northeasterly within the Piedmont
province. The basins are aligned subparallel to the Appalachian terranes (Figure 5-1)
and formed along pre-existing zones of faulting and then subsided during a period of
crustal stretching (Olsen, Froelich, Daniels, Smoot, & Gore, 1991). The Dan River Basin
is located in the western belt of rift basins and is bounded on the southeast by the
Milton terrane and on the northwest by the Sauratown Mountains Anticlinorium and
the Smith River allochthon (Figure 5-1; (Horton, Jr., Drake, Jr., & Rankin, 1989);
(Hibbard, Stoddard, Secor, & Dennis, 2002); (Hatcher, Jr., Bream, & Merschat, 2007)).
The Sauratown Mountains Anticlinorium consists of four stacked thrust sheets and
subsequent erosion has exposed a complex, multitiered window or exposure of these
thrust sheets (Horton & McConnell, 1991). A complex sequence of interlayered and
faulted calc-silicate gneiss, biotite-augen gneiss, quartz-feldspar gneiss, epidosite, and
amphibolite characterize the anticlinorium (Horton & McConnell, 1991). The Smith
River allochthon consists predominately of biotite gneiss in North Carolina (Horton &
McConnell, 1991).
The fractured bedrock is overlain by a mantle of unconsolidated material known as
regolith. The regolith includes residual soil and saprolite zones and, where present,
alluvial deposits. Saprolite, the product of chemical weathering of the underlying
bedrock, is typically composed of clay and coarser granular material and reflects the
texture and structure of the rock from which it was formed. The weathering products of
granitic rocks are quartz-rich and sandy textured. Rocks poor in quartz and rich in
feldspar and ferro-magnesium minerals form a more clayey saprolite (LeGrand, 2004).
The degree of weathering decreases with depth and partially weathered rock (PWR) is
commonly present near the top of the bedrock surface. The transition zone from the
regolith and the PWR and competent bedrock is often gradational and difficult to
differentiate.
Regional Hydrogeology 5.2
The groundwater system in the Piedmont Province, in most cases, is comprised of two
interconnected layers, or mediums: 1) residual soil/saprolite and weathered fractured
rock (regolith) overlying 2) fractured crystalline bedrock (Heath R. , 1980); (Harned &
Daniel, 1992). The regolith layer is a thoroughly weathered and structureless residual
soil that occurs near the ground surface with the degree of weathering decreasing with
depth. The residual soil grades into saprolite, a coarser grained material that retains the
structure of the parent bedrock. Beneath the saprolite, partially weathered/fractured
bedrock occurs with depth until sound bedrock is encountered. This mantle of residual
soil, saprolite, and weathered/fractured rock is a hydrogeologic unit that covers and
crosses various types of rock (LeGrand, 1988). This layer serves as the shallow
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unconfined groundwater system and provides an intergranular medium through which
the recharge and discharge of water from the underlying fractured rock occurs. Within
the fractured crystalline bedrock layer, the fractures control both the hydraulic
conductivity and storage capacity of the rock mass. A transition zone (TZ) at the base of
the regolith has been interpreted to be present in many areas of the Piedmont. Harned
and Daniel (1992) describe the TZ as consisting of partially weathered/fractured
bedrock and lesser amounts of saprolite that grades into bedrock. They also describe the
TZ as “being the most permeable part of the system, even slightly more permeable than
the soil zone” (Harned & Daniel, 1992). Harned and Daniel (1992) suggested the zone
may serve as a conduit of rapid flow and transmission of contaminated water.
Until recently, most of the information supporting the existence of the TZ was
qualitative based on observations made during the drilling of boreholes and water-
wells, although some quantitative data is available for the Piedmont region (Stewart,
1964a); (Nutter & Otton); (Harned & Daniel, 1992). Using a database of 669 horizontal
conductivity measurements in boreholes at six locations in the Carolina Piedmont,
Schaeffer (Schaeffer, 2014a) statistically showed that a TZ of higher hydraulic
conductivity exists in the Piedmont groundwater system when considered within
Harned and Daniel’s (1992) two types of bedrock conceptual framework.
The TZ is comprised of partially weathered rock, open, steeply dipping fractures, and
low angle stress relief fractures, either singly or in various combinations below refusal
(auger, roller cone, or casing advancer; (Schaeffer, 2011); (2014b). The TZ has less
advanced weathering relative to the regolith and generally the weathering has not
progressed to the development of clay minerals that would decrease the permeability of
secondary porosity developed during weathering, (i.e., new fractures developed during
the weathering process, and /or the enhancement of existing fractures). The
characteristics of the TZ can vary widely based on the interaction of rock type, degree of
weathering, degree of systematic fracturing, presence of stress-relief fracturing, and the
general characteristics of the bedrock (foliated/layered, massive, or in between). The TZ
is not a continuous layer between the regolith and bedrock; it thins and thickens within
short distances and is absent in places (Schaeffer, 2011); (2014b). The absence, thinning,
and thickening of the TZ is related to the characteristics of the underlying bedrock
(Schaeffer, 2014b).
The TZ may vary due to different rock types and associated rock structure. Harned and
Daniel divided the bedrock into two conceptual models: 1) foliated/layered
(metasedimentary and metavolcanic sequences) and 2) massive/plutonic (plutonic and
metaplutonic complexes) structures (Harned & Daniel, 1992). Strongly foliated/layered
rocks are thought to have a well-developed TZ due to the breakup and weathering
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along the foliation planes or layering, resulting in numerous rock fragments (Harned &
Daniel, 1992). More massive/plutonic rocks are thought to develop an indistinct TZ
because they do not contain foliation/layering and tend to weather along relatively
widely spaced fractures (Harned & Daniel, 1992). Schaeffer (Schaeffer, 2014a) proved
Harned and Daniel’s (Harned & Daniel, 1992) hypothesis that foliated/layered bedrock
would have a better developed transition zone than plutonic/massive bedrock. The
foliated/layered bedrock transition zone has a statistically significant higher hydraulic
conductivity than the massive/plutonic bedrock transition zone (Schaeffer, 2014a).
LeGrand’s (1988); (1989) conceptual model of the groundwater setting in the Piedmont,
applicable to the BCSS site, incorporates the Daniel and Harned (1992) two-medium
regolith/bedrock system into an entity that is useful for the description of groundwater
conditions. That entity is the surface drainage basin that contains a perennial stream
(LeGrand, 1988). Each basin is similar to adjacent basins and the conditions are
generally repetitive from basin to basin. Within a basin, movement of groundwater is
generally restricted to the area extending from the drainage divides to a perennial
stream (Slope-Aquifer System; Figure 5-3; (LeGrand, 1988); (1989); (2004). Rarely does
groundwater move beneath a perennial stream to another more distant stream or across
drainage divides (LeGrand, 1989). The crests of the water table underneath topographic
drainage divides represent natural groundwater divides within the slope-aquifer
system and may limit the area of influence of wells or contaminant plumes located
within their boundaries. The concave topographic areas between the topographic
divides may be considered as flow compartments that are open-ended down slope.
Therefore, the groundwater system is a two-medium system restricted to the local
drainage basin. The groundwater occurs in a system composed of two interconnected
layers: residual soil/saprolite and weathered rock overlying fractured crystalline rock
separated by the TZ. Typically, the residual soil/saprolite is partially saturated and the
water table fluctuates within it. Water movement is generally preferential through the
weathered/fractured and fractured bedrock of the TZ (i.e., enhanced permeability zone).
The character of such layers results from the combined effects of the rock type, fracture
system, topography, and weathering. Topography exerts an influence on both
weathering and the opening of fractures, while the weathering of the crystalline rock
modifies both transmissive and storage characteristics.
The igneous and metamorphic bedrock in the Piedmont consists of interlocking crystals
and primary porosity is very low, generally less than 3 percent. Secondary porosity of
crystalline bedrock due to weathering and fractures ranges from 1 to 10 percent (Freeze
& Cherry, 1979); but, porosity values of 1 to 3 percent are more typical (Daniel III &
Sharpless). Daniel (1992) reported that the porosity of the regolith ranges from 35 to 55
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percent near land surface but decreases with depth as the degree of weathering
decreases.
In natural areas, groundwater flow paths in the Piedmont are almost invariably
restricted to the zone underlying the topographic slope extending from a topographic
divide to an adjacent stream. Under natural conditions, the general direction of
groundwater flow can be approximated from the surface topography (LeGrand, 2004).
Groundwater recharge in the Piedmont is derived entirely from infiltration of local
precipitation. Groundwater recharge occurs in areas of higher topography (i.e., hilltops)
and groundwater discharge occurs in lowland areas bordering surface water bodies,
marshes, and floodplains (LeGrand, 2004). Average annual precipitation contributing to
recharge in the Piedmont ranges from 42 to 46 inches. Mean annual recharge in the
Piedmont ranges from 4.0 to 9.7 inches per year (Daniel, 2001).
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6.0 SITE GEOLOGY AND HYDROGEOLOGY
Geology beneath the BCSS site can be classified into three units. Regolith (surficial
soils, fill and reworked soil, and saprolite) is the shallowest geologic unit. A transition
zone of partially weathered rock underlies the regolith (where present, the saprolite is
the lowest portion of the regolith) and is generally continuous throughout the BCSS site.
The third unit, competent bedrock, is defined by rock core recovery, RQD and the
degree of fracturing in the rock. Typically, mildly productive fractures (providing
water to wells) were observed within the top 50 feet of competent rock.
In general, three hydrogeologic units or zones of groundwater flow can be described for
the BCSS Site. The zone closest to the surface is the shallow flow layer encompassing
saturated conditions, where present, in the residual soil or saprolite beneath the Site. A
transition zone (deep flow layer) is encountered below the shallow flow layer and
above the bedrock, is characterized primarily by partially weathered rock of variable
thickness. The bedrock flow layer occurs below the transition zone and is characterized
by the storage and transmission of groundwater in water-bearing fractures.
Site investigations included performing soil borings, collection of soil and rock cores,
groundwater monitoring wells, borings installed in the ash basin for the sampling of
ash pore water. Physical and chemical properties of soil samples collected from the
borings and wells are presented in Tables 6-1 through 6-3, respectively. The analytical
methods used with solid and aqueous samples are presented in Table 6-4 and Table 6-
5. Table 2-1 summarizes the well construction data for CAMA-related wells and
piezometers at the Site. Strategic locations for anchoring flow path transects were
selected. Boring logs, well construction records and well abandonment records for
CAMA-related monitoring installations are included in Appendix F. Primary technical
objectives for the sampling locations included: the development of additional
background data on groundwater quality; the determination of horizontal and vertical
extent of impact to soil and groundwater; and the establishment of perimeter boundary
conditions for groundwater modeling that will be used to develop a CAP.
The BCSS ash basin acts as a bowl-like feature which groundwater flows towards.
Groundwater then flows from the basin to the east, northeast, northwest but primarily
north towards the Dan River. Groundwater at the Site flows away from the
topographic and hydrologic divide (highest topographic portion of the Site) generally
located along Pine Hall Road to the north towards the ash basin and south towards
Belews Reservoir.
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Three transects were selected to illustrate flow path conditions in the vicinity of the ash
basin. Section A-A’ is a transverse section through the ash basin, parallel to
groundwater flow. Section B-B’ illustrates conditions perpendicular to groundwater
flow, traversing from west to east across the site. Section C-C’ is a traverse south to
north along the western edge of the ash basin.
Site Geology 6.1
The BCSS site and its associated ash basin are located in the Milton terrane. The Milton
terrane is characterized by strongly foliated gneisses and schists, commonly with
distinct compositional layering and felsic composition; quartzite, calc-silicate gneiss,
hornblende gneiss and schist, and marble are minor units (Carpenter III, 1982); (Butler
& Secor, 1991); (Schaeffer, 2001)). The majority of the rocks in the belt are
metamorphosed to the sillimanite and kyanite grade of amphibolite metamorphism
(Butler & Secor, 1991). The Dan River Triassic Basin is located approximately 3,000 feet
north of the site.
Geologic units mapped in the vicinity of the site include alluvium, terrace deposits,
sedimentary rocks of the Dan River Basin, a diabase dike, and felsic gneisses and schists
with interlayered hornblende gneiss and schist (Figure 6-1; Schaeffer 2001). The
alluvium consists of unconsolidated sand, silt, and clay with occasional sub-rounded to
well-rounded pebbles and cobbles. The terrace deposits consist of unconsolidated sand,
silt, and clay with pebbles and cobles of quartz. In places, the terrace deposits are
comprised of large angular quartz fragments in a red matrix of sand, silt, and clay. The
diabase occurs in a long, relatively thin dike. The rocks of the Milton terrane in the area
include interlayered augen gneiss, quartz-feldspar gneiss, flaser gneiss, “button” mica
schist, and with interlayers of hornblende gneiss and schist (Schaeffer, 2001). The
installed well and sample locations are shown in Figure 2-10.
Soil Classification 6.1.1
Regolith was encountered from a depth range of a few inches to 66 feet at BCSS
outside the ash basin. Beneath the ash basin soil samples were collected from 28
to 81.5 feet. The following soils/materials were encountered in the boreholes:
Ash – Ash was encountered in borings advanced within the ash basin.
Ash was generally described as gray to dark gray, non-plastic, loose to
medium dense, dry to wet, fine- to coarse-grained, consistent with fly ash
and bottom ash.
Fill – Fill material was used in the construction of the ash basin dikes and
dam, and generally consisted of re-worked silts, clays, and sands that
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were borrowed from the site and re-distributed to other areas. Fill was
generally classified as silty sand, clay with sand, clay, and sandy clay on
the boring logs.
Residuum (Residual soils) – Residuum is the in-place weathered soil that
consists primarily of silt with sand, clayey sand, sandy clay, clay with
gravel, and clayey silts. Residuum varied in thickness and was relatively
thin compared to the thickness of saprolite.
Saprolite/Weathered Rock – Saprolite is soil developed by in-place
weathering of rock that retains remnant bedrock structure. Saprolite
consisted primarily of medium dense to very dense silty sand, sandy silt,
sand, sand with gravel, sand with clay, clay with sand, and clay. Sand
particle size ranged from fine to coarse-grained. Much of the saprolite was
micaceous.
Alluvial deposits were not encountered in any of the new boreholes or in any of
the historic boreholes in the area of the BCSS ash basin. Alluvial deposits were
mapped downstream of the ash basin main dam and along the Dan River (Figure
6-1).
Geotechnical index property testing of the above soil/materials was performed
for disturbed and undisturbed samples in accordance with ASTM standards.
Thirty-six undisturbed ('Shelby Tube') samples were submitted for geotechnical
index testing. Index property testing for undisturbed samples comprised Unified
Soil Classification System (USCS) classification (ASTM, 2001)), natural moisture
content (ASTM, 2010), Atterberg Limits (ATSM, 2010), grain size distribution,
including sieve analysis and hydrometer (ASTM, 2007), total porosity calculated
from specific gravity (ASTM, 2010), and hydraulic conductivity (ASTM, 2010).
One undisturbed sample was unable to receive the full suite of index property
tests due to low recovery, wax and gravel mixed in the tube, loose material, or
damaged tubes. Eighteen disturbed ('Split Spoon,' or 'Jar') samples received grain
size distribution with hydrometer (ASTM, 2007), and natural moisture content
(ASTM, 2010).
Results from the geotechnical property testing show background soil samples
collected at BCSS range from silty sand to sandy silt. Natural moisture content in
the background soil samples is as low as 15.2% (sandy silt) and as high as 40.3%
(silty sand). Specific gravity values for the background soil samples are between
2.597 and 2.753. High levels of fine sand, silt, and clay are present in all
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background soil samples, while low levels of gravel are present in the silty sand
samples. Soil samples collected from downgradient boreholes are characterized
as silty sand to sandy silt. Downgradient soil samples have natural moisture
content levels from 12.2% to 38.7%. Similar to the background soil samples, the
downgradient soil samples have a specific gravity range of 2.6 to 2.764. While the
downgradient samples are mainly comprised of fine sand, silt and clay, fine
gravel is also present in many of the samples. All soil property results are shown
in Table 3-2.
Rock Lithology 6.1.2
The main rock types in the immediate vicinity of the ash pond are mica schist,
schistose mica gneiss, augen gneiss, flaser gneiss, quartz-feldspar gneiss, biotite
gneiss, and hornblende schist and gneiss. The mica schist is coarse-grained, well
foliated, “button” schist composed of muscovite and quartz with pinhead
garnets. Interlayered with the “button” schist are layers of mica schist (non-
“button”) and fine- to medium-grained schistose mica gneiss. The augen gneiss
is a fine- to medium-grained rock with a well-developed foliation that wraps
around conspicuous pods or “eyes” of feldspar and to a lesser extent quartz.
They are comprised mainly of quartz, feldspar, and mica. The flaser gneiss
consists of small lenses or granular materials (quartz-feldspar-mica) separated by
wavy ribbons and streaks of finely crystalline, foliated materials (primarily
mica). The quartz-feldspar gneiss is a medium- to coarse-grained, foliated,
normally mica-poor rock although some massive varieties (less foliated) have up
to 15 percent muscovite. The biotite gneiss is fine- to medium-grained, banded
rock consisting of alternating layers of biotite-rich zones and quartz/feldspar-rich
zones. The hornblende gneiss and schist is a fine- to coarse-grained, dark colored
rock composed of hornblende, biotite, and plagioclase. It is semi-massive to well-
foliated and occurs as interlayers in the predominantly felsic rock sequence.
A diabase dike has been mapped from the right abutment of the main ash basin
dike and extends to the north cutting across the above rock types and the
sedimentary rocks of the Dan River Basin. The diabase dike is fine- to medium-
grained and consists of pyroxene, hornblende, and plagioclase with minor
amounts of olivine (Schaeffer, 2001).
Structural Geology 6.1.3
All the rock types are interlayered and the felsic rocks grade laterally and
vertically into each other. The contacts of the hornblende gneiss/schist with the
felsic rock are generally sharp. Compositional layer is generally parallel to the
strongly developed foliation. The orientation of foliation is relatively consistent
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throughout the area (N72E; 56SE). The presence of “button” schist, augen gneiss,
and flaser gneiss indicates that the rocks have been strongly deformed and
sheared during at least two episodes of isoclinal folding (Schaeffer, 2001);
“buttons” are formed by the intersection of two, nearly parallel, axial planar
foliations). The deformation related to folding was ductile, although the presence
of thin layers of flaser gneiss indicates that some of the deformation occurred
under semi-brittle to brittle conditions (Schaeffer, 2001).
Data on the orientation of fractures in the underlying bedrock in the area is
sparse due to relatively poor bedrock exposures. Schaeffer (2001) observed three
joint sets in outcrops: (1) N20-40W with steep dips (>70o), (2) N to N20E with
steep dips (>70o); and (3) a set sub-parallel to layering/foliation N60-75E with
dips ranging from 30o to vertical. Very few joints are present in the mica schist. In
contrast, the gneissic rocks tend to have more fractures, and the hornblende
gneisses and schists have few fractures associated with them compared to the
felsic rocks (Schaeffer, 2001). The joints are generally clay-filled in the
saprolite/weathered zone above the transition zone (Schaeffer, 2001).
Soil and Rock Mineralogy and Chemistry 6.1.4
Soil mineralogy and chemistry analyses are complete and the results are shown
in Table 6-1 (mineralogy), Table 6-2 (chemistry, % oxides), and Table 6-3
(chemistry, elemental composition). Completed laboratory analyses of the
mineralogy and chemical composition of TZ materials are presented in Tables 6-
6 (mineralogy), 6-7 (chemistry, % oxides), and 6-8 (chemistry, elemental). Rock
chemistry results are presented in Table 6-9 (chemistry, % oxides) and Table 6-
10 (chemistry, elemental). All mineralogy reports can be found in Appendix C.
The petrographic analysis of seven rock samples (thin-sections) are presented in
Table 6-11 (mineralogy).
The mineralogical analyses of BCSS soils varied slightly between 23 boring
locations but mineralogical composition indicates the dominant minerals in the
soils are quartz, feldspar (both alkali and plagioclase feldspars), kaolinite, illite,
and muscovite/illite. Other minerals identified include vermiculite/illite, biotite,
smectite, chlorite, and amorphous smectites, mica, and iron oxide/hydroxide.
Mineralogy results from six TZ samples are comparable to the soil results. The
dominant minerals remain quartz, feldspar (both alkali and plagioclase
feldspars), illite, kaolinite, and biotite.
At BG-2D, a background well located northeast of the ash basin with 55 feet of
saprolitic regolith, the mineral assemblage consisted of predominately quartz
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and clay minerals with 65% quartz, 15% kaolinite, 5% plagioclase feldspar, and
5% vermiculite 5% chlorite, 3% smectite and 2% mica. In comparison, the
mineralogical data at AB-3D from a sample recovered from 50 feet in saprolitic
regolith below the ash basin includes a similar mineralogical composition of 74%
quartz, 10% kaolinite, 2% plagioclase feldspar, and 3% vermiculite, 1% smectite
and 10% mica. The similarities in extent of saprolitic depths at boring locations
and mineralogical composition suggest uniform regolith conditions across the
site.
Elemental chemistry of BCSS soils shows highest concentrations of zinc,
vanadium, strontium and tin. Other elements identified in most samples are
chromium, copper, cobalt, lead and nickel. Elemental chemistry results for all
samples from both the TZ and whole rock samples indicate uniform highest
concentrations of cerium, zinc, gallium, and lanthanum compared to other
elements analyzed. Other elements identified in most samples are copper, cobalt,
nickel and lead. The whole rock chemistry of GWA-2D shows the highest
concentrations of each element analyzed compared to the other samples collected
at BCSS. This location, northeast of the ash basin, shows arsenic concentrations of
17 ppm in the TZ and 24 ppm in bedrock which are elevated relative to all other
samples which range from 1 to 9 ppm of Arsenic.
Oxide results from each layer show SiO2, Al2O3, and Fe2O3 as the three dominate
oxide compositions for all samples analyzed at BCSS:
Soil oxide composition: SiO2 (47.20% - 74.97%), Al2O3 (12.18% -26.40%),
and Fe2O3 (2.78% - 12.00%)
Transition zone oxide composition: SiO2 (64.92% - 72.01%), Al2O3 (13.17% -
16.65%), and Fe2O3 (2.96% - 6.39%)
Whole rock oxide composition: SiO2 (63.4% - 74.3%), Al2O3 (15.4% - 21.7%)
and Fe2O3 (2.5% - 8.0%)
Results also indicate a significant composition of MnO from both the BCSS soils
and transition zone with ranges from 0.03% to 0.10% for soils and 0.05% to 0.14%
for transition zone.
Geologic Mapping 6.1.5
Duke Engineering & Services (2001) and Schaeffer (2001) prepared a detailed
geologic map of the area surrounding the BCSS ash basin for expansion of an
existing on-site landfill as shown on Figure 6-1. The rock(s) encountered in the
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boreholes for the monitoring wells and pre-existing wells are shown on Figure 6-
1.
Effects of Geologic Structure on Groundwater Flow 6.1.6
The most important effects of structural geology on groundwater flow would be
preferential flow along the contacts (~N72E) and along the joints within the
bedrock. The north-trending diabase dike could either form a barrier to flow or a
flow path depending on its degree of fracturing and weathering both of which
are not known. A non-fractured diabase dike would be a flow barrier and would
direct groundwater flow along its contact. A fractured, weathered dike could act
as a flow channel. The extent of the diabase dike under the ash to the south of the
main dam is not known, but it does not extend south of the ash basin based on
the geologic mapping (Figure 6-1)
Site Hydrogeology 6.2
According to LeGrand, the soil/saprolite regolith and the underlying fractured bedrock
represent a composite water-table aquifer system (LeGrand 2002). The regolith
provides the majority of water storage in the Piedmont province, with porosities that
range from 35 to 55 percent (Daniel & Dahlen, 2002). Calculated porosities specific to
the Site (43.4% to 47.3%)are consistent with this range. Two major factors that influence
the behavior of groundwater in the vicinity of the Site include the thickness (or
occurrence) of saprolite/regolith and the hydraulic properties of underlying bedrock.
Saprolite thickness varies across the Site but is generally thickest in upgradient areas (20
to 60 feet for GWA-8S and MW-202S) and thins in downgradient areas near the Dan
River (5 to 12 feet for GWA-24S and MW-200s).
Based on the site investigation, the groundwater system in natural materials (soil,
soil/saprolite, and bedrock) at the BCSS site is consistent with the regolith-fractured
rock system and is an unconfined, connected aquifer system as discussed in Section 5.2.
Regolith is underlain by a transition zone (TZ) of weathered rock which transitions to
competent bedrock. The groundwater system at the BCSS site is divided into three flow
layers referred to in this report as the shallow, deep (TZ), and bedrock layers, so as to
distinguish unique characteristics of the connected aquifer system.
Hydrostrographic Layer Development 6.2.1
The hydrostratigraphic classification system of Schaeffer (Schaeffer, 2014a) was
used to evaluate natural system hydrostratigraphic layer properties. The
classification system is based on Standard Penetration Testing values (N) and the
Recovery (REC) and Rock Quality Designation (RQD) collected during the
drilling and logging of the boreholes (Borehole/Well logs in Appendix F). The
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Schaeffer classification system uses of the terms M1 and M2 to classify saprolite
material with the M2 designation indicating greater competency. A transition
zone of weathered, fractured rock is delineated between overlying saprolite and
underlying bedrock based on rock core recovery (REC) and rock quality
designation (RQD). The bedrock zone is classified as having REC>85% and
RQD>50%.
For discussion purposes, hydrostratigraphic units will be recognized in the text
and supporting documents as follows:
Shallow Unit – Alluvium/Saprolite (S wells)
Deep Unit – Saprolite and weathered rock (D wells)
Bedrock Unit – Sound rock, relatively unfractured (BR wells)
The shallow zone generally corresponds to the M1 unit and the deep zone
incorporates the M2 and weathered, fractured rock layers. Bedrock is identified
per the REC and RQD criteria.
The designations ash, fill, saprolite, transition zone and bedrock are used on the
geologic cross-sections with locations shown on Figure 6-2. Generalized cross
sections are presented in Figures 6-3 to 6-5 showing site geology and
groundwater flow directions.
Hydrostrographic Layer Properties 6.2.2
Ash Pore water
The ash pore water unit consists of saturated ash material. Ash depths range
from a few feet to approximately 66 feet. The full pond elevation of the BCSS ash
basin is approximately 750 feet, yielding approximately 55 feet of saturated ash
in the thickest ash locations.
Shallow Flow Layer
The shallow flow layer consists of regolith (soil/saprolite) material. Thickness of
regolith is directly related to topography, type of parent rock, and geologic
history. Topographic highs tend to exhibit thinner soil-saprolite zones, while
topographic lows typically contain thicker soil-saprolite zones. Wells within the
shallow flow layer that are installed within shallow wells contain an “S”
designation.
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Deep Flow Layer
The deep flow layer (transition zone) consists of a relatively transmissive zone of
partially weathered bedrock. Observations of core recovered from this zone
included rock fragments, unconsolidated material, and highly oxidized bedrock
material. Deep flow layer wells are labeled with a “D” designation.
Bedrock Flow Layer
The fractured bedrock unit occurs within competent bedrock. Bedrock in the
immediate vicinity of the ash basin are mica schist, schistose mica gneiss, augen
gneiss, flaser gneiss, quartz-feldspar gneiss, biotite gneiss, and hornblende schist
and gneiss. The majority of water producing fracture zones was found within 50
feet of the top of competent rock. Water-bearing fractures encountered are only
mildly productive (providing water to wells). Bedrock wells are labeled with a
“BR” designation.
Groundwater Flow Direction 6.3
Based on the CSA site investigation, groundwater flow is generally to the north and
northwest in the direction of the Dan River. Groundwater also flows south of the
topographic ridge, which follows Pine Hall Road, towards Belews Reservoir.
Voluntary, compliance, and groundwater assessment monitoring wells were gauged for
depth to water within a 24- hour period during comprehensive groundwater elevation
measurement events on September 20, 2016 and April 3, 2017 to provide water level
elevation data for dry and wet season (respectively) at the Site. Depth to water
measurements were subtracted from surveyed top of well casing elevations to produce
groundwater elevations in shallow, deep, and bedrock monitoring wells (Table 6-12).
Groundwater flow direction was estimated by contouring these groundwater
elevations.
Groundwater flow at the BCSS follows the local slope aquifer system (Figure 5-3), as
described by LeGrand (LeGrand, 2004)). In general, groundwater within the shallow
wells (S), wells in the TZ (D), and wells in fractured bedrock (BR) flows northerly from
the ash basin toward the Dan River. A groundwater divide is located approximately
along Pine Hall and to the west of the ash basin along Middleton Loop Road. Another
groundwater divide exists north of the ash basin along a ridgeline that extends from the
east dike abutment toward the northeast. These groundwater divides generally
correspond to the topographic divides in these locations. The predominant direction of
groundwater flow from the ash basin is in a northerly direction toward the valley where
the designated effluent channel flows from the base of the ash basin dam northwest to
the Dan River and to the east toward Belews Reservoir.
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During full-operations (prior to dry ash handling) sluicing to the basin would have had
an impact contaminant inputs to the basin. As fly ash production moved to a dry
process (1984) the basin water input would have decreased as containment load would
have begun to decrease. Beginning in 2018 basin water input should decrease and
therefore further reduce containment load. With bulk water removal through
dewatering, recharge and containment loading should return to pre-development
levels, including groundwater flow patterns.
The shallow, deep and bedrock water level maps during September 2016 and April 2017
are included as Figures 6-6 through 6-11.
Hydraulic Gradient 6.4
Horizontal hydraulic gradients were derived for April 2017 water levels measurements
in the shallow, TZ, and fractured bedrock wells by calculating the difference in
hydraulic head over the length of the flow path between two wells with similar well
construction (e.g., wells within the same water-bearing unit). The following equation
was used to calculate horizontal hydraulic gradient:
i = dh / dl
Where i is the hydraulic gradient; dh is the difference between two hydraulic heads
(measured in feet); and dl is the flow path length between the two wells (measured in
feet)
Applying this equation to wells installed during the CSA activities yields the following
average horizontal hydraulic gradients (measured in feet/foot):
Shallow wells: 0.009 ft/ft
Deep wells: 0.010 ft/ft
Bedrock wells: 0.019 ft/ft
Generally horizontal gradients in the ash basin range from 0.002 to 0.004 ft/ft.
Horizontal gradients outside the waste boundary range from 0.006 to 0.035 ft/ft. The
hydraulic gradient south of the ash basin (GWA-12BR to MW-202BR) and northwest of
the dam (GWA-16S to GWA-11S) is likely due to the much higher relief between the
basin and downgradient areas. A summary of horizontal hydraulic gradient
calculations is presented in Table 6-13.
Vertical hydraulic gradients were calculated by taking the difference in groundwater
elevation in a deep and shallow well pair over the difference in total well depth of the
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deep and shallow well pair. A positive output indicates downward flow and a negative
output indicates upward flow. Vertical gradient calculations for 32 shallow and deep
well pair locations and 9 deep to bedrock well pair locations, were used to calculate
vertical hydraulic gradient across the site. Applying this calculation to wells installed
during the CSA activities yields the following average vertical hydraulic gradients
(measured in feet/foot):
Shallow to Deep wells: 0.0195 ft/ft
Deep to Bedrock wells: 0.0967 ft/ft
Based on review of the results, vertical gradients were mixed across the site but with
more locations showing downward gradient values. More upward values were noted
south of the ash basin and the topographic high of Pine Hall Road near Belews
Reservoir (GWA-12, GWA-23, and BG-3 locations), downgradient of the basin near the
Dan River (GWA-30 and GWA-31) and northeast of the basin (BG-2). Vertical gradient
calculations are summarized in Table 6-14 and shown in Figure 6-12.
Hydraulic Conductivity 6.5
Hydraulic conductivity (slug) tests were completed in monitoring wells. Slug tests were
performed to meet the requirements of the May 31, 2007 NCDENR Memorandum titled,
Performance and Analysis of Aquifer Slug Tests and Pumping Tests Policy. Water level
change during the slug tests was recorded by a data logger. The slug test was
performed for no less than 10 minutes, or until such time as the water level in the test
well recovered 95 percent of its original pre-test level, whichever occurred first. Slug
tests were terminated after 60 minutes even if the 95 percent pre-test level was not
achieved. Slug test field data was analyzed using the Aqtesolv (or similar) software and
the Bouwer and Rice method. These previously reported horizontal and vertical
groundwater conductivity results are presented in Table 6-15 and 6-16.
Additionally, in situ hydraulic conductivities were calculated using slug test results
reported in CSA Supplement 2 (HDR, 2016c) (Appendix C) to determine groundwater
velocity by grouping hydraulic conductivity (slug) test data into their respective
hydrostratigraphic units and calculating the geometric mean, maximum and minimum.
Hydrostratigraphic layers are defined in Section 11.1. Hydraulic conductivity values for
wells screened in saprolite have a geometric mean of 2.65 x 10-4 cm/sec. Hydraulic
conductivity values for wells screened in the transition zone have a geometric mean of
7.91 x 10-5 cm/sec. These measurements reflect the dynamic nature of the transition
zone, where hydrologic properties can be heavily influenced by the formation of clays
and other weathering by-products. Hydraulic conductivity results for bedrock wells
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across the Site have a geometric mean of 2.76 x 10-5 cm/sec . The hydraulic conductivity
measurements in bedrock wells can be regarded as a generalized representation of the
localized bedrock fractures in specific areas of a well cluster.
In situ horizontal hydraulic conductivity values for each hydrostratigraphic unit
established are in Table 6-17.
Groundwater Velocity 6.6
To calculate the velocity that water moves through a porous media, the specific
discharge, or Darcy flux, is divided by the effective porosity, ne. The result is the
average linear velocity or seepage velocity of groundwater between two points.
Groundwater flow velocities for the surficial and transition flow zones were calculated
using Darcy's Law equation which describes the flow rate or flux of fluid through a
porous media by the following formula: 𝑣𝑣𝑠𝑠 = Ki/ne
𝑣𝑣𝑠𝑠 = seepage velocity, K = horizontal hydraulic conductivity, i = the horizontal
hydraulic gradient; and ne = effective porosity.
Seepage velocities for groundwater were calculated using horizontal hydraulic
gradients established by grouping hydraulic conductivity (slug) test data into their
respective hydrostratigraphic units and calculating the geometric mean, maximum and
minimum.
Horizontal hydraulic conductivity values for each hydrostratigraphic unit established
in Table 6-17, and effective porosity values established in Tables 6-18 and 6-19.
Hydrogeologic porosity reports are provided in Appendix C. Hydrostratigraphic layers
are defined in Section 11.1. Average groundwater seepage velocity results are
summarized in Table 6-13.
At BCSS, groundwater movement in the bedrock flow zone is primarily due to
secondary porosity represented by fractures in the bedrock. Primary (matrix) porosity
is negligible; therefore, it is not technically appropriate to calculate groundwater
velocity using effective porosity values and the method presented above. Bedrock
fractures encountered at BCSS tend to be isolated with low interconnectivity. Further,
hydraulic conductivity values measure the fractures immediately adjacent to a well
screen, not across the distance between two bedrock wells. Groundwater flow in
bedrock fractures is anisotropic and difficult to predict, and velocities change as
groundwater moves between factures of varying orientations, gradients, pressure, and
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size. For these reasons, bedrock groundwater velocities calculated using the seepage
velocity equation are not representative of actual site conditions and were not
calculated. For additional information on the movement of groundwater around and
downgradient of the Ash Basin over time, refer to discussion concerning groundwater
fate and transport modeling (Section 13.0).
Contaminant Velocity 6.7
Migration, retardation, and attenuation of COIs in the subsurface is a factor of both
physical and chemical properties of the media in which the groundwater passes. Soil
samples were collected and analyzed for grain size, total porosity, soil sorption (Kd),
and anions/cations to provide data necessary for completion of the three-dimensional
groundwater model discussed in Section 13.
The pore water in the ash basin is the source of constituents reported greater than
background concentrations, 2L standards, and IMACs in groundwater samples in the
vicinity of the ash basins. Gradients measured within the ash basin support the
interpretation that ash pore water mixes with shallow/surficial groundwater and
migrates downward into the transition zone and bedrock flow zones. Continued
vertical migration of groundwater is also evidenced by detected constituent
concentrations.
Boron is relatively mobile in groundwater and is associated with low Kd values. This is
primarily because boron is mostly inert, has limited potential for sorption, and lacks an
affinity to form complexes with other ions. In general, the low Kd measured for boron
allows the constituent to move at a similar velocity to groundwater. The higher Kd
values measured for the remaining metals, like thallium and cobalt, agree with the
limited migration of these constituents. Constituents like cobalt and thallium have
much higher Kd values, and will move at a much slower velocity than groundwater as it
sorbs onto surrounding soil.
Groundwater migrates under diffuse flow conditions in the shallow and deep aquifer in
the direction of the prevailing gradient. As constituents enter the transition zone
material, the rate of constituent transport has the potential to increase from 7.66 x10-6
cm/sec in the shallow zone to 1.62 x10-05 cm/sec in transition zone, as demonstrated by
groundwater seepage velocity results (Table 6-13). It should be noted that the fractured
bedrock flow system is highly heterogeneous in nature and high permeability zones
with a geomean in situ horizontal conductivity of 0.00003 cm/sec observed, but these
hydraulic conductivity measurements measure the fractures immediately adjacent to a
well screen, not across the distance between two bedrock wells and cannot be applied
across the entire Site. Geochemical mechanisms controlling the migration of
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constituents are discussed further in Section 13. Groundwater modeling to be
performed for the updated CAP will include a discussion of contaminant velocities for
the modeled constituents.
Slug Test and Aquifer Test Results 6.8
In-situ horizontal (open hole) and vertical (flush bottom) permeability tests, either
falling or constant head as appropriate for field conditions, were performed in each of
the hydrostratigraphic units above refusal, ash, fill, and soil/saprolite. In-situ borehole
horizontal permeability tests, either falling or constant head tests as appropriate for
field conditions, were performed just below refusal in the first 5 feet of a rock cored
borehole (TZ, if present).
The flush bottom test involves advancing the borehole through the overburden with a
casing advancer until the test interval is reached. The cutting tool is removed from the
casing and the casing is filled with water to the top and the water level drop in the
casing is measured over 60 minutes. In the open hole test, after the top of the test
interval is reached, the cutting tool but not the casing, is advanced an additional
number of feet (five feet in the majority of tests) and water level drop in the casing is
measured over 60 minutes. The constant head test is similar except the water level is
kept at a constant level in the casing and the water flow-in is measured over 60 minutes.
The constant head test was only used when the water level in the borehole was
dropping too quickly back to the static water level such that the time interval was
insufficient to calculate the hydraulic conductivity. The results from the field
permeability testing are summarized in Table 6-20 and the worksheets are provided in
Appendix C.
Packer tests (shut-in and pressure tests) were conducted in a minimum of five
boreholes. The shut-in test is performed by isolating the zone between the packers (in
effect, a piezometer) and measuring the resulting water level over time until the water
level is stable. The shut-in test provides an estimate of the vertical gradient during the
test interval. The pressure test involves forcing water under pressure into rock through
the walls of the borehole providing a means of determining the apparent horizontal
hydraulic conductivity of the bedrock. Each interval is tested at three pressures with
three steps of 20 minutes up and two steps of 5 minutes back down. The pressure test
results are summarized in Table 6-20 and the shut-in and packer tests worksheets are
provided in Appendix C.
Where possible, tests were conducted at borehole locations specified in the Work Plan
and at test intervals based on site-specific conditions at the time of the groundwater
assessment work. The U.S. Bureau of Reclamation test method and calculation
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procedures, as described in Chapter 10 of their Ground Water Manual (1995), were used
for the field permeability and packer tests. Historic field permeability and
packer/pressure test data for the BCSS site are presented in Table 6-21.
Fracture Trace Study Results (if applicable) 6.9
Fracture trace analysis is a remote sensing technique used to identify lineaments on
topographic maps and aerial photography that may correlate to locations of bedrock
fractures exposed at the earth’s surface. Although fracture trace analysis is a useful tool
for identifying potential fracture locations, and hence potential preferential pathways
for infiltration and flow of groundwater near a site, results are not definitive.
Lineaments identified as part of fracture trace analysis may or may not correspond to
actual locations of fractures exposed at the surface, and if fractures are present, it cannot
be determined from fracture trace analysis whether these are open or healed. Healed
fractures intruded by diabase are common in the vicinity of the site.
Strong linear features at the earth’s surface are commonly formed by weathering along
steeply dipping to vertical fractures in bedrock. Morphological features such as narrow,
sharp-crested ridges, narrow linear valleys, linear escarpments, and linear segments of
streams otherwise characterized by dendritic patterns are examples. Linear variations in
vegetative cover are also sometimes indicative of the presence of exposed fractures,
though in many cases these result from unrelated human activity or other geological
considerations (e.g., change in lithology).
Straight (as opposed to curvilinear) features are commonly associated with the presence
of steeply dipping fractures. Curvilinear features in some cases are associated with
exposed moderately-dipping fractures, but these also can be a result of preferential
weathering along lithologic contacts, or along foliation planes or other geologic
structure. As part of this study, only strongly linear features were considered, as these
are far more commonly indicative of steeply dipping or vertical fractures.
The effectiveness of fracture-trace analysis in the eastern United States, including in the
Piedmont, is commonly hampered by the presence of dense vegetative cover, and often
extensive land-surface modification owing to present and past human activity. Aerial-
photography interpretation is most affected, as identification of small-scale features can
be rendered difficult or impossible in developed areas.
Methods 6.9.1
Available geologic maps for the area were consulted prior to performance of
aerial-photography and topographic-map interpretation, to identify lithologies
and geologic structure in the area that can control fracture occurrence and
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orientations. Topographic-map interpretation was performed over an area of
approximately 22 square miles, and aerial-photography interpretation was
performed over an area of approximately 5 square miles.
Topographic-map interpretation involved examination of the Belews Creek, N.C.
1:24,000-scale USGS 7.5-minute topographic quadrangle. A digital copy of the
quadrangle was obtained and viewed on a monitor at up to 7x magnification.
Lineaments identified were plotted directly on the digital images.
Photography provided for review included 1”= 600’ scale, 9 x 9 inch black-and-
white (grayscale) contact prints dated April 17, 2014.The photography was
examined using a Lietz Sokkia MS-27 mirror stereoscope with magnifying
binocular eyepiece. Lineaments identified on the photographs were marked on
hard copies of scanned images (600dpi resolution), and subsequently compiled
onto a photomosaic base.
Results 6.9.2
Lineaments identified from topographic maps are shown and lineament trends
indicated by a rose diagram are included on Figure 6-13. A total of 35
topographic lineaments were identified across the study area, mainly north,
west, and southwest of the site. The prevalent trend is toward the northwest,
with subsidiary trends toward the north, northeast, and west-northwest. The
north and northwest trending lineaments are in general agreement with
orientations of Triassic diabase dikes and with the N20-40W and N-N20E joint
sets discussed in Section 6.1.3. The northeast and west-northwest trending
lineaments correlate well with foliation and joint trends in the Milton terrane
rocks that underlie the study area (Figure 6-1).
Lineaments identified from aerial photography are shown and lineament trends
indicated by a rose diagram are included on Figure 6-14. A total of 25 lineaments
were identified. These were primarily in the form of linear morphological highs,
linear morphological lows (linear stream valleys, ravines, and gullies), and light-
colored linear outcrops of the Milton terrane rocks.
Generally, the lineament trends from the aerial photography correlate with those
identified from topographic-map interpretation. Relatively fewer northwest-
trending lineaments, and more north-trending lineaments (both being
subparallel to regional diabase dike orientations) were identified on aerial
photography. Few west-northwest trending lineaments were identified, and
northeast trending lineaments identified on aerial photography are oriented
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primarily N25E as opposed to N40E for those identified from topographic-map
interpretation.
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7.0 SOIL SAMPLING RESULTS
Soil, PWR, and bedrock samples were collected from background locations, beneath the
ash basin, and from locations beyond the waste boundary. The purpose of soil and rock
characterization is to evaluate the physical and geochemical properties in the subsurface
with regard to COI presence, retardation, and migration. Soil and rock sampling was
performed in general accordance with the procedures described in the Work Plan
utilized for groundwater assessment activities. Refer to Appendix G for a detailed
description of these methods and Appendix G for field and sampling quality control /
quality assurance protocols.
Table 6-4 summarizes the parameters and constituent analytical methods for soil, PWR,
and bedrock samples collected. Total inorganic results for background soil, PWR, and
bedrock samples can be found in Appendix B, Table 4. Soil borings were conducted in
upgradient and downgradient (laterally and vertically) areas of the ash basins in order
to collect soil samples from the unsaturated zone and the zone of saturation for these
areas (Figure 2-10). Cross-section transects are presented in plan view on Figure 6-2
and with vertical distribution COIs along each transect depicted on Figures 11-4
through 11-63.
BCSS does not have SPLP results for background soil samples. Regional background
soil SPLP results are averaged for comparison and are presented in Table 3-3. Although
SPLP analytical results are being compared to the 2L Standards or IMAC, these samples
do not represent groundwater samples.
Background Soil Data 7.1
Because some COIs are naturally occurring in soil and are present in the source areas,
establishing background concentrations is important for determining whether releases
have occurred from the source areas. Background (BG) boring locations were identified
based on the Site Conceptual Model at the time the Work Plan was submitted and
approved. The background locations (BG-1, BG-2, BG-3 and GWA-12) were chosen in
areas believed not to be impacted by CCR leachate based on existing knowledge of the
site and topographically upgradient of the ash basin. Based on the groundwater
contours shown in Figures 6-6 through 6-11, and the Site Conceptual Model, the
background locations are considered to be hydrologically upgradient of the ash basin.
As a result, the background boring locations are considered to be representative of
background soil and rock conditions at the BCSS site.
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An updated background soil dataset was provided to NCDEQ for BCSS on May 26,
2017. Additionally, the revised Statistical Methods for Developing Reference Background
Concentrations for Groundwater and Soil at Coal Ash Facilities (statistical methods
document) (HDR and SynTerra, 2017) was provided to NCDEQ. On July 7, 2017,
NCDEQ provided a response letter (Zimmerman to Draovitch, July 7, 2017) for each
Duke Energy coal ash facility that identified soil and groundwater data appropriate for
inclusion in the statistical analysis to determine provisional background threshold
values (PBTVs) for both media (Appendix A). As outlined in the NCDEQ July 7, 2017
letter, Duke Energy was required to provide PBTVs for each media within 30 days from
receipt of the NCDEQ letter for facilities submitting CSAs by October 31, 2017.
NCDEQ requested that Duke Energy collect a minimum of 10, rather than the
previously planned eight, valid background samples prior to the determination of
PBTVs for each constituent.
The background dataset provided to NCDEQ on May 26, 2017 included pooled soil
samples collected from multiple depth intervals. Only samples collected from
background locations at depth intervals greater than one foot above the seasonal high
water table were included in the dataset. The background soil dataset has been further
revised from the May 26, 2017 submittal based on input from NCDEQ in the July 7, 2017
letter.
Additional soil samples were collected on July 26, 2017 to satisfy the minimum number
of soil samples and to provide values for antimony, selenium and thallium below the
PSRG Protection of Groundwater values (Figure 2-10). The dataset was screened for
outliers once the additional samples were included in the dataset Table 7-1. The soil
background dataset and PBTVs were sent to NCDEQ in an Updated Background
Threshold Values for Soil Technical Memorandum dated August 30, 2017 and approved
by NCDEQ DWR in a response letter (Zimmerman to Draovitch) dated September 1,
2017 (Appendix A).
PBTVs for soil constituents are provided in Table 7-2. Boring logs associated with the
additional soil samples are included in Appendix F.
Facility Soil Data 7.2
Soil samples were collected during CSA monitoring well installations. Comparison of
soil analytical results with background is discussed below based on the area of the Site.
Soil Beneath the Ash Basin
Soil samples within the ash basin waste boundary (including dams) were obtained from
AB-1S, AB-2D/GTB, AB-3S/D, AB-4D, AB-5D, AB-6D/GTB, AB-7D, AB-8D, and AB-
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9S/D. The range of constituent concentrations in soils beneath the ash basin and within
the waste boundary, along with a comparison to soil PBTVs is provided in Appendix B,
Table 4. Geotechnical borings (GTB) were utilized at the BCSS site to supplement soil
data needs in a temporary boring used only for collection purposes (i.e., no monitoring
wells were installed at these locations).
Although some constituent levels were measured above Industrial preliminary soil
remediation goals (PSRG) and PSRG for protection of groundwater (POG) standards in
soil samples beneath the basin, when compared to the Site’s PBTVs most constituent
levels appeared to be similar to calculated soil background values for the Site. For soil
samples below the ash, arsenic and chromium were reported at concentrations that
exceeded the Industrial PSRG. Arsenic, boron, chromium, cobalt, iron, manganese,
selenium and vanadium had reported values above the PSRG for POG. All soil samples
beneath the ash basin that had PSRG exceedances were greater than or equal to those in
the ash. Boron concentrations were not detected greater than the PSRG values or the
Site PBTV (17 mg/kg) below the ash basin. Of the PSRG exceedances, concentrations of
six arsenic samples and one selenium sample exceeded the respective PBTV for the Site.
The exceedances are depicted on Figure 7-1. Soil sample test results indicate shallow
impacts to the soil beneath the ash basin
Soil Beyond the Waste Boundary
Soil samples outside the waste boundary were obtained from GWA-1S, GWA-2D,
GWA-3S/D, GWA-4S, GWA-5S/GTB, GWA-6S, GWA-7S, GWA-8D, GWA-9S/GTB,
GWA-10D, GWA-11D, GWA-12D, MW-200BR, MW-203BR, and SB-3. The range of
constituent concentrations in soils outside the waste boundary, along with a
comparison to the range of reported background soil concentrations, is provided in
Appendix B, Table 4.
Constituent concentrations for soils outside the waste boundary tend to be similar to
background soil concentrations for all constituents with the exception of barium and
cobalt (but are within one order of magnitude). The barium concentration at GWA-
9GTB (a geotechnical boring located near the GWA-9 well cluster) and cobalt
concentrations at SB-3 for the singular soil sample were above the POG PSRGs and
account for the upper ranges for these constituents. All other barium and cobalt
concentrations obtained outside the waste boundary were similar to those measured at
background locations.
Additionally, arsenic and chromium had concentrations above the Industrial PSRG in
several soil sample locations. Detected concentrations of arsenic, chromium, cobalt,
iron, manganese, selenium and vanadium in multiple locations exceeded the PSRG for
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POG. Several of the arsenic and iron soil concentrations that exceeded PSRG standards
also exceeded the PBTV. Three locations, GWA-6S (68.5-70), GWA-9S (50-52) and GWA-
11D (55-55.4), had concentrations of iron that exceeded the PBTV. Locations GWA-6S
(68.5-70) exceeded the PBTV for chromium and GWA-7S (30-31.5) exceeded the PBTV
for selenium. Concentrations of boron from wells beyond the compliance boundary did
not exceed PSRG values and only two locations exceeded the PBTV at GWA-6S and
MW-200BR. The majority of exceedances are sporadic and do not indicate the ash basin
as a source of soil impacts beyond the waste boundary.
Comparison of PWR and Bedrock Results to Background
Samples were obtained from locations ouside the waste boundary; two PWR samples at
BG-1S and GWA-3D, and three bedrock samples at BG-2D, MW-200BR, and MW-
203BR,. The range of constituent concentrations in PWR and bedrock samples outside
the waste boundary, along with a comparison to the reported PBTV, is provided in
Appendix B, Table 4. Chromium exceeded the Industrial PSRG and POG for two of the
rock samples. Arsenic, iron, manganese, and vanadium exceeded the PSRG POG in four
of the samples. Of the PSRG exceedances, the chromium concentration from MW-203BR
is the only exceedance above the PBTV (41.09 mg/kg).
Secondary Sources
Soil samples were collected during assessment activities from areas beneath the ash
basin, and outside the ash basin and within the compliance boundary. Concentrations
of arsenic, barium, chloride, chloride, chromium, cobalt, iron, selenium, strontium and
vanadium in soils were found to be greater than the POG PSRGs or PBTV for one or
more sample locations.
Soils beneath the ash basin were found to have exceedances of the POG PSRGs and/or
PBTVs limited to a shallow interval beneath the basin. Arsenic, selenium and strontium
exceeded the PBTV in at least one soil sample beneath the ash basin. Constituent
concentrations often decrease with depth in borings beneath the ash basin. Constituent
occurrences in areas outside the ash basin may exceed site-specific PBTVs but elevated
concentrations of chromium, iron, strontium and vanadium in areas upgradient of the
ash basin (GWA-6S, GWA-7S and GWA-8D) are not influenced by the ash basin and
associated with natural soil geochemistry. Saturation and other factors may also affect
constituent occurrence in the samples.
Geochemical modeling which will be included in the CAP is anticipated to help in
determining constituent association with coal ash and an appropriate site remedy if
necessary. The locations to be evaluated for site remedy are depicted on Figure 7-1.
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8.0 SEDIMENT RESULTS
Sediment samples were collected from 19 locations beyond the perimeter of the ash
basin (Figure 2-10) during and after the 2015 CSA field effort. Sediment sampling
procedures and variances are provided in Appendix G and analytical results are
presented in Appendix B, Table 5.
Sediment/Surface Soil Associated with AOWs 8.1
Eleven of the 19 sediment sampling locations were co-located with designated Areas of
Wetness (AOWs). The “sediment” that was collected was actually surface soil over
which water at the AOW was flowing or seeping. Sediment samples were collected on
October 5 and 8, 2015 (Round 2).
Four of the 19 sediment sample locations were co-located with NCDENR March 2014
water sample locations (BCSW-007, BCSW-008, BCSW-018A, and BCSW019). These
locations are stormwater outfalls to Belews Reservoir. It is assumed that the sediment
collected from these locations was actually surface soil over which water was flowing or
seeping. Sediment samples were collected on October 5, 2015 (Round 2). The
remaining 4 sediment samples were collected beneath Belews Reservoir and are
discussed in Section 8.2.
The sediment sample results were compared to North Carolina PSRGs for POG, and are
presented in Appendix B, Table 5. Sediment sample locations are shown on Figure 2-
10. A description of AOWs S-1 through S-11 and the results of sediment analysis are
provided below, as well as the results of sediment analysis for locations BCSW-007,
BCSW-008, BCSW-018A, and BCSW-019:
S-1: Steady flow emerging from several springs within channel that appears to
follow natural topography that trends away from a ridge separating the ash
basin from the apparent drainage area. Sediment was collected from the channel.
No constituents exceeded their PBTVs for soil. Cobalt, iron, manganese and
vanadium concentrations exceeded their PSRGs for POG.
S-2: Steady flow within ravine channel that appears to follow natural topography
that trends away from a ridge separating the ash basin from the apparent
drainage area. Flow is continuous but occasionally it disappears and reappears
from the ground surface. Sediment was collected from the channel. No
constituents exceeded their PBTVs for soil. Arsenic, chromium, cobalt, iron,
manganese and vanadium concentrations exceeded their PSRGs for POG.
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S-3: Steady continuous flow within ravine channel appears to follow natural
topography that trends away from a ridge separating the ash basin from the
apparent drainage area. Sediment was collected from the channel. The
concentration of arsenic exceeds the soil PBTV. Arsenic, chromium, cobalt, iron,
manganese and vanadium concentrations exceeded their PSRGs for POG.
S-4: Steady continuous flow within ravine channel appears to follow natural
topography that trends away from a ridge separating the ash basin from the
apparent drainage area. Sediment was collected from channel. No PSRG values
are established for strontium and this is the only constituent that exceeded the
PBTV at this location. Chromium, cobalt, iron, manganese and vanadium
concentrations exceeded their PSRGs for POG.
S-5: Steady continuous flow within ravine channel appears to follow natural
topography that trends away from a ridge separating the ash basin from the
apparent drainage area. Sediment was collected from the channel. The
concentration of arsenic exceeds the soil PBTV. Arsenic, chromium, cobalt, iron,
manganese and vanadium concentrations exceeded their PSRGs for POG. Boron
was detected in this sample.
S-6: Moderate flow of clear water emerging from toe of dam below the ash basin
former outfall and berm. Sediment collected from the channel. Concentrations of
nickel, strontium, sulfate and zinc exceed their soil PBTVs. Chromium, cobalt,
iron, manganese, selenium and vanadium concentrations exceeded their PSRGs
for POG. Boron was detected in this sample.
S-7: Low flow wide area with shallow water depth. Sediment collected beneath
inundated area. The concentration of arsenic exceeds the soil PBTV. Arsenic,
chromium, cobalt, iron, manganese and vanadium concentrations exceeded their
PSRGs for POG.
S-8: Well defined stream approximately 2.5 feet wide and 3 to 4 inches deep on
average with a sandy substrate. Sediment was collected from stream bed. No
constituents exceeded their soil PBTVs. Chromium, iron, manganese and
vanadium concentrations exceeded the PSRG for POG. Boron was detected in
this sample.
S-9: Steady trickle to moderately flow clear water stream. Sediment was
collected from the stream bed. No constituents exceeded their soil PBTVs.
Chromium, iron, manganese and vanadium concentrations exceeded the PSRG
for POG.
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S-10: Flow emerging from downstream terminus of wetland areas on west side
of the base of the ash basin dam. Sediment was collected from the channel. The
concentrations of arsenic and strontium exceed their soil PBTVs. Arsenic,
chromium, cobalt, iron, manganese and vanadium concentrations exceeded their
PSRGs for POG. Boron was detected in this sample.
S-11: Flow originates from piping that captures flow from main ash basin dam.
Sediment collected from channel. Aluminum, arsenic and nickel concentrations
exceeded their soil PBTVs. Arsenic, chromium, cobalt, iron, manganese and
vanadium concentrations exceeded their PSRGs for POG. Boron was detected in
this sample.
BCSW-007: Sample is located southeast of the ash basin and the plant near
Belews Reservoir. Copper, barium, nickel, selenium and strontium
concentrations exceeded their respective soil PBTVs. Arsenic, chromium, cobalt,
iron, manganese, selenium and vanadium concentrations exceeded their PSRGs
for POG.
BCSW-008: Sample is located west of the FGD Residue Landfill near Belews
Reservoir. No PSRG values are established for sulfate and this is the only
constituent that exceeded the PBTV at this location. Chromium, cobalt, iron,
manganese, selenium and vanadium concentrations exceeded their PSRGs for
POG. Boron was detected in this sample.
BCSW-018A: Sample is located southeast of the structural fill near Belews
Reservoir. No constituents exceeded their PBTVs. Chromium, cobalt, iron,
manganese, selenium and vanadium concentrations exceeded their PSRGs for
POG.
BCSW-19: Sample is located south of the ash basin downgradient from AOW
location S-9. No constituents exceeded their soil PBTVs. Chromium
concentration exceeded both the Industrial PSRG and POG. Cobalt, iron,
manganese and vanadium concentrations exceeded the PSRG POG. Boron was
detected in this sample.
Sediment in Major Water Bodies 8.2
Sediment samples were collected coincidentally with the surface water samples along
the shore line of the Dan River (SD-DR-U and SD-DR-D) and Belews Reservoir (SD-BL-
U and SD-BL-D) during CSA sampling Round 1 (July 2015).
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Sediment samples were analyzed in accordance with the constituent and parameter list
used for soil and rock characterization (Table 6-4). In the absence of NCDEQ sediment
criteria, the sediment sample results were compared to North Carolina PSRGs and soil
PBTVs, and are presented in Appendix B, Table 5. Sediment sample locations are
shown on Figure 2-10.
Exceedances of the PSRGs for POG in the sediment samples included chromium (SD-
DR-U, SD-DR-D, and SD-BL-U), cobalt (SD-DR-D), iron (all samples), manganese (SD-
DR-U, SD-DR-D, and SD-BL-D), selenium (SD-DR-D), and vanadium (all samples).
Sample SD-DR-D exceeded the PBTV for chloride where no PSRG value has been
established. Sample SD-DR-U had four exceedances (chromium, iron, manganese, and
vanadium) while the downstream sample had seven exceedances (arsenic, chromium,
cobalt, iron, manganese, selenium, and vanadium). Sample SD-DR-D also had boron
detected in the sample. Sample SD-BL-U had three exceedances (chromium, iron and
vanadium) while the downstream sample had four exceedances (chromium, iron,
manganese and vanadium). None of the PSRG exceedances were greater than the
PBTVs.
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9.0 SURFACE WATER RESULTS
The BCSS ash basin is located in the central part of the BCSS site and receives surface
water runoff and groundwater recharge from upland areas south of the basin.
Groundwater from the ash basin flows downgradient of the ash basin dam
predominately through the designated effluent channel, discharging to the Dan River
(NPDES outfall 003). Surface water analytical results associated with samples collected
from the Dan River and Belews Reservoir are included in Appendix B, Table 2. The
surface water sample locations are included on Figure 2-10. Aqueous matrix parameters
and analytical methods are shown on Table 6-5.
As shown Figures 10-5 to 10-64, the extent of groundwater migration from the ash basin
at concentrations greater than background and 2L extend downgradient of the ash basin
but do not reach the Dan River or Belews Reservoir. Therefore, the surface water data
reflect contributions from sources other than groundwater migration from the ash
basin.
Water samples discussed within the following sections include four distinct types: 1)
ash basin wastewater and wastewater conveyance (effluent channels), 2) areas of
wetness (AOWs), 3) industrial stormwater, and 4) named surface waters. For this CSA,
it is pertinent that a comparison with NCDENR Title 15A, Subchapter 02B. Surface
Water and Wetland Standards (2B) standards includes only sample results from named
surface waters. AOWs, wastewater and wastewater conveyances (effluent channels),
and industrial storm water are evaluated and regulated in accordance with the NPDES
Program administered by NCDEQ DWR. This process is on-going in a parallel effort to
the CSA and subject to change.
Ash Basin Water Samples
Water samples (SW-1, SW-1A, SW-2, and SW-AB1 through SW-AB9) were collected
from water ponded within the ash basin. Sample SW-10 is located downstream of the
ash basin main dam in the designated effluent channel. This sample is also considered
to be representative of ash basin water. The ash basin water is not considered surface
water or groundwater and the results are presented for discussion purposes only. Ash
basin water sample locations are shown on Figure 2-10 and analytical results are listed
in Appendix B, Table 3.
Belews Creek Area of Wetness (AOW) Sample Locations
Sixteen AOWs (S-1 through S-16) have been identified and sampled routinely for
monitoring purposes. Eleven AOWs (S-1 through S-11) were identified and sampled as
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part of the 2015 CSA. The BCSS site is inspected semi-annually for the presence of
existing and potentially new AOWs along the Belews Reservoir shoreline,
downgradient of the ash basin, including observations by boat and by land. Inspections
by land included observations of the ash basin along toe of the dikes; areas below full
pond elevation for the ash basin; between the ash basin and receiving waters; and
drainage features associated with the basin including engineered channels. Per the
interim administrative agreement, these inspections are governed by the Discharge
Identification Plan (DIP) until the NPDES permit is issued. AOW locations S-12, S-13, S-
14, S-15, and S-16 were identified after the 2015 CSA sampling effort.
These locations are being evaluated for separately in accordance with the NPDES
permit and do not have applicable criteria. The analytical results of these samples are
for discussion purposes only. AOW sample locations are shown on Figure 2-10 and
analytical results are listed in Appendix B, Table 3.
Dan River and Belews Reservoir Sample Locations
Dan River sample SW-DR-BG collected upstream of the confluence of the ash basin
designated effluent channel (outfall 003) with the Dan River outside of the Duke Energy
property boundary is considered to be representative of background surface water
quality conditions in the river. Dan River sample SW-DR-U was collected immediately
upstream of the confluence of the ash basin designated effluent channel (outfall 003)
with the Dan River and sample SW-DR-D was collected immediately downstream of
the confluence.
Sample SW-DR-U has had contaminant concentrations reported as being greater than
the background surface water sample (and reported 2B surface water standard
exceedances), which suggests that there may be influence from the ash basin at this
location along the Dan River. However, contaminant concentrations detected in SW-
DR-U were similar to those in sample 003, collected at the ash basin discharge structure
flume in the designated effluent channel, indicating that the location of sample SW-DR-
U may be too close to the designated effluent channel to reflect actual water quality in
the Dan River.
Eleven additional water samples (S-003-D, S-2-D, S-3-D, S-5-D, SW-DR-1, SW-DR-2,
SW-DR-3, SW-DR-4, SW-DR-BG, SW-DR-D and SW-DR-UA) were collected from the
Dan River in September 2017 to refine the understanding the potential source of 2B
exceedances detected in the river at SW-DR-U.
Surface water samples (SW-DR-U, SW-DR-D and SW-DR-BG) were intended to be
collected from the Dan River from there previously sampled locations as conditions
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permitted. Surface water sample SW-DR-U was inadvertently collected further
upstream than intended and therefore has been identified as a unique sample location
(SW-DR-UA).
Samples S-2-D, S-3-D, S-5-D were collected downstream of their respective AOW
sample locations from the streams prior to their confluence with the Dan River. Sample
S-003-D was collected downstream of sample 003 from the designated effluent channel
at the confluence with the Dan River. These sample results do not have applicable
criteria and the analytical results of these samples are for discussion purposes only.
Surface water samples SW-DR-1, SW-DR-2, SW-DR-3, and SW-DR-4 were collected
from the Dan River between the stream channels to evaluate whether the tributaries
were potentially influencing water quality in the Dan River.
Upstream and downstream surface water samples were collected from Belews
Reservoir (SW-BL-U and SW-BL-D). The upstream sample location (SW-BL-U), on the
south shore of Belews Reservoir upstream of the Craig Road Landfill, is considered to
be representative of background surface water quality conditions in the lake. The
downstream Belews Reservoir sample location (SW-BL-D), located west of a boat ramp
on the north shore of Belews Reservoir, is considered to be downstream of potential
impacts from the ash basin.
NCDEQ Sample Locations
NCDENR collected water samples from 13 locations at BCSS during March 2014 (Figure
2-10). Analytical results are provided in Appendix B, Table 3. The locations and
analytical results from this sampling event were provided by NCDEQ to Duke Energy
and are assumed to be accurate. Prior to the dam reinforcement construction activities,
water from the ash basin embankment and foundation was captured in a series of
horizontal drains (HD) and engineered flumes (TF) before being routed through a
Parshall flume for NCDEQ Dam Safety flow monitoring at the toe of the dam (ABW).
Water sample identifiers and location relative to former and current site features are:
TF-1, TF-2, TF-3, HD-07A, HD-09, HD-10, HD-11A, HD-21, HD-22, HD-24, HD-
25, HD-26, HD-27, ABW (base of ash basin dam; primarily monitoring discharge
from toe drains installed within the structural fill of the embankment dam)
003 (ash basin discharge structure flume)
BCWW-002 (FGD wastewater treatment plant effluent)
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BCSW-018A and BCSW-019 (stormwater outfalls adjacent to railroad tracks near
Belews Reservoir)
BCSW-08 (stormwater outfall adjacent to FGD Landfill)
Samples TF-1, TF-2, TF-3, HD-07A, HD-09, HD-10, HD-11A, HD-21, HD-22, HD-24,
HD-25, HD-26, HD-27 and ABW, are representative of ash basin water, the sample
results do not have applicable criteria and are presented for discussion purposes only.
As a result of dam reinforcement activities, the embankment drainage system is now
connected to a single discharge point. Therefore, monitoring the previous toe drainage
locations is no longer possible. Sample BCWW-002 was collected from the FGD
wastewater treatment plant effluent and is wastewater and therefore is not evaluated
with regards to exceedances of regulatory standards or background concentrations.
Samples BC-018A, BCSW-019, and BCSW-08 are stormwater outfalls and these locations
do not have applicable criteria and are presented for discussion purposes only.
Comparison of Exceedances to 2B Criteria 9.1
The following surface water sample locations occur in the Dan River and are compared
to 2B (Class WS-IV) values.
SW-DR-BG, S-2D, SW-DR-1, S-3D, SW-DR-2, S-5D, SW-DR-3, SW-DR-UA, SW-
DR-U, SW-DR-D, and SW-DR-4.
The following surface water sample locations occur in Belews Reservoir and are
compared to 15A NCAC 02B (Class C) values.
SW-BL-U and SW-BL-D
SW-DR-BG and SW-BL-U are considered background surface water quality locations
with regards to the downgradient samples collected on the Dan River (SW-DR-1, SW-
DR-2, SW-DR-3, SW-DR-UA, SW-DR-U, SW-DR-D, and SW-DR-4) and from Belews
Reservoir (SW-BL-D), respectively. Therefore, in addition to comparing downstream
surface water results with the 2B standards they are also compared with the
background surface water location results. The background surface water
concentrations have not been statistically derived or approved by NCDEQ and are for
discussion purposes only.
Analytical results with the dissolved phase concentrations greater than their associated
total reportable concentrations are not included in the assessment as they are
considered invalid.
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Data presented below lists the sample ID, the constituent that has been reported with a
2B exceedance, and the number of reported 2B exceedances over the number of
sampling events in parenthesis:
Dan River Samples
SW-DR-BG: (Dan River background sample): No 2B exceedances (0/2)
SW-DR-1: No 2B exceedances (0/1)
SW-DR-2: No 2B exceedances (0/1)
SW-DR-3: No 2B exceedances (0/1)
SW-DR-UA: No 2B exceedances (0/1)
SW-DR-U: pH (1/8), Turbidity (2/8), DO (1/8), Chloride (1/8), Selenium (2/8), TDS
(2/8), Dissolved Cadmium (1/8), Dissolved Lead (1/8)
SW-DR-D: pH (1/9), Turbidity (2/9), Chloride (2/9), Selenium (2/9), TDS (3/9),
Dissolved Cadmium (1/8), Dissolved Lead (1/8)
SW-DR-4: No 2B exceedances
Sample results from the Dan River indicate that field parameters (turbidity, pH, and
DO), total concentrations of chloride, selenium, and TDS, dissolved concentrations
(cadmium and lead) have been reported as being greater than 2B values on one or two
occasions, but not consistently.
Belews Reservoir Samples
No 2B exceedance have been reported in the samples (SW-BL-U and SW-BL-D)
collected from Belews Reservoir over the period of monitoring.
Discussion of Results for Constituents Without Established 2B 9.2
A 2B standard has not been established for a number of constituents. A summary of
results for select constituents without 2B standards follows. The results are compared
with the background surface water data. The background surface water concentrations
have not been statistically derived or approved by NCDEQ and are for discussion
purposes only.
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Dan River Samples
Antimony was not detected in the Dan River background sample at a
concentration greater than the MDL (<0.5 µg/L to 1 µg/L). The reported
antimony concentrations in the downgradient sample location have been within
the range of the reported background concentrations.
Boron has not been detected in the Dan River background sample or upstream of
the effluent channel confluence. Concentrations of boron at SW-DR-U, SW-DR-
D, and SW-DR-4 have been greater than background.
Cobalt was reported in the Dan River background sample at a concentration of
0.14 µg/L. During the second sampling event of the background location cobalt
was not detected at the MDL (<1 µg/L). Concentrations of cobalt at SW-DR-U
and SW-DR-D have exceeded the background concentration range for cobalt.
Cobalt has not been detected at the remaining sample locations.
Chromium was not detected in the Dan River background sample at a
concentration greater than the MDL (<0.5 to <1 µg/L). Concentrations of
chromium at SW-DR-U and SW-DR-D have exceeded the background
concentration range for chromium. Chromium has not been detected at the
remaining sample locations.
Hexavalent chromium concentrations were reported at 0.06 µg/L at the Dan
River background sample location. Concentrations of hexavalent chromium at
SW-DR-3, SW-DR-4, and SW-DR-U have exceeded the background concentration
for chromium. The remaining sample locations have had concentrations reported
as being less than the background concentration.
Iron concentrations range from 459 µg/L to 589 µg/L at the Dan River
background sample location. Concentrations of iron at SW-DR-D and SW-DR-U
have exceeded the background concentration range for iron. The remaining
sample locations have had concentrations reported as being less than the
background concentration range.
Manganese concentrations range from 51.2 µg/L to 65 µg/L at the Dan River
background sample location. Concentrations of manganese at SW-DR-D and
SW-DR-U have exceeded the background concentration range for manganese.
The remaining sample locations have had concentrations reported as being less
than the background concentration range.
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Thallium was not detected at the Dan River background sample at a
concentration greater than the MDL (<0.1 to <0.2 µg/L). Concentrations of
thallium at SW-DR-D and SW-DR-U have exceeded the background
concentration range for thallium. Thallium has not been detected at the
remaining sample locations.
Vanadium concentrations were reported at 1 µg/L at the Dan River background
sample location. Concentrations of vanadium at SW-DR-2, SW-DR-3, SW-DR-4,
SW-DR-D and SW-DR-U have exceeded the background concentration for
vanadium. The remaining sample locations have had concentrations reported as
being less than the background concentration.
Belews Reservoir Samples
Antimony concentrations range from 0.1 µg/L to <0.5 µg/L in the Belews
Reservoir background sample location. The reported antimony concentrations at
the downgradient sample location have been within the range of the reported
background concentrations.
Boron concentrations range from 25.4 µg/L to 71 µg/L in the Belews Reservoir
background sample location. The reported downgradient boron concentrations
have generally been in the range of the background concentrations with the
exception of one sampling event with a result of 72 µg/L.
Cobalt concentrations range from 0.01 µg/L to <0.5 µg/L in the Belews Reservoir
background sample location. The reported cobalt concentrations at the
downgradient sample location have been within the range of the reported
background concentrations.
Chromium concentrations range from 0.097 µg/L to 0.37 µg/L in the Belews
Reservoir background sample location. The reported downgradient chromium
concentrations have generally been in the range of the background
concentrations with the exception of two sampling events with results of 0.38
and 0.7 µg/L.
Hexavalent chromium concentrations range from 0.026 µg/L to 0.12 µg/L in the
Belews Reservoir background sample location. The reported hexavalent
chromium concentrations at the downgradient sample location have been within
the range of the reported background concentrations.
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Iron concentrations range from 39.7 µg/L to 235 µg/L in the Belews Reservoir
background sample location. The reported iron concentrations at the
downgradient sample location have been within the range of the reported
background concentrations.
Manganese concentrations range from 6.2 µg/L to 24.3 µg/L in the Belews
Reservoir background sample location. The reported manganese concentrations
at the downgradient sample location have been within the range of the reported
background concentrations.
Thallium concentrations range from 0.018 µg/L to <0.1 µg/L in the Belews
Reservoir background sample location. The reported thallium concentrations at
the downgradient sample location have been within the range of the reported
background concentrations.
Vanadium concentrations range from 0.48 µg/L to 0.89 µg/L in the Belews
Reservoir background sample location. The reported downgradient vanadium
concentrations have generally been in the range of the background
concentrations with the exception of two sampling events with results of 0.94
and 1 µg/L.
Discussion of Surface Water Results 9.3
Dan River
Dan River samples SW-DR-U and SW-DR-D have had reported 2B exceedances of
turbidity, pH, DO, chloride, selenium, TDS, dissolved cadmium, and dissolved lead.
The 2B exceedances have all been greater than the concentrations reported in
background sample SW-DR-BG, which does not have any 2B exceedances reported.
Dan River sample SW-DR-U was collected immediately upstream of the confluence of
the ash basin designated effluent channel with the Dan River, and sample SW-DR-D
was collected immediately downstream of the confluence.
Water samples SW-DR-1, SW-DR-2, SW-DR-3, and SW-DR-UA were collected from the
Dan River in September 2017 between background sample location SW-DR-BG and the
SW-DR-U location to refine the understanding the potential source of 2B exceedances
reported at SW-DR-U.
Exceedances of the 2B standards were not reported in any of the surface water samples
collected between SW-DR-BG and SW-DR-UA. A sample was inadvertently not
collected from SW-DR-U during the September 2017 sampling event; however it
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appears that the 2B exceedances reported in SW-DR-U (and SW-DR-D) are a result of
the proximity to the designated effluent channel (outfall 003). The sampling results do
not suggest that the reported 2B exceedances in the Dan River are a result of influence
from the ash basin.
Belews Reservoir
No 2B exceedance have been reported in the samples (SW-BL-U and SW-BL-D)
collected from Belews Reservoir over the period of monitoring. Based on the available
data for the upstream and downstream Belews Reservoir samples the BCSS ash basin is
not the source of 2B exceedances in Belews Reservoir.
To help determine potential routes of exposure and receptors related to the ash basin,
additional surface water samples will be collected from Belews Reservoir and the Dan
River near the stream/river bank most likely to be impacted by potentially
contaminated groundwater discharge. The additional surface water sampling effort is
described in detail in Section 11.3.
Piper diagrams, a graphical representation of major water chemistry using two ternary
plots and a diamond plot, for AOWs and surface water are included as Figure 9-1 and
9-2. A Piper diagram is a graphical representation of major water chemistry using two
ternary plots and a diamond plot. One of the ternary plots shows the relative
percentage of major cations in individual water samples, and the other shows the
relative percentage of the major anions. Piper diagrams for groundwater monitoring
wells are presented and discussed in more detail in Section 10.0.
Piper diagram for AOWs, engineered drains below the dam and surface water locations
compared to background surface water (SW-DR-BG) concentrations are presented as
Figure 9-1 and 9-2. Observations based on the diagram include:
Waters at BCSS are predominately characterized as calcium-chloride bicarbonate
water type, with AOW samples from locations S-1, S-8, S-12, S-13, S-15, and
surface water locations SW-BL-D and SW-DR-U consistent with those of
background waters at BCSS.
Upgradient AOW S-9 exhibits higher relative concentrations of sulfate compared
with other AOW water types. This location is south of the ash basin and the
topographic ridge that divides groundwater flow north and south. The unique
water type may be associated with impact from the structural fill. An assessment
of the structural fill is ongoing.
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Locations S-2, S-4, S-6/ S-6-BL, S-9, S-10 and S-11 indicate potential mixing
between background water and impacted AOW waters.
Outfall locations and surface water collected from engineered drains below the
dam are representative of impacted surface water. Water type from those
locations are characterized as chloride-sodium and chloride-bicarbonate. Higher
concentrations of chloride relative to the concentration of sulfate indicate mixing
of source area water with different basin sources; however the ash basin shows
higher concentrations of chloride in water samples than waters that may be
influenced from other basins on site. Samples BCSW-008 and BCSW-019 are
upgradient of the ash basin and show less chloride impact in water samples.
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10.0 GROUNDWATER SAMPLING RESULTS
This section provides a summary of groundwater analytical results for the most recent
monitoring event through April 2017 (2Q2017) with discussion of historical data result
and trends. A comprehensive table with all media analytical sampling results is
provided in Appendix B, Table 1. Most recent and historical groundwater laboratory
reports are presented in Appendix I. The current monitoring well network at the site is
presented on Figure 2-10. As indicated on the comprehensive data table, for
groundwater results, the results have been marked to indicate data points excluded
based on a measured turbidity greater than 10 NTUs; high pH values that may indicate
possible grout intrusion into the well screen; and data that may be auto-correlated
because it was collected within 60 days of a previous sampling event. The most recent
data available through April 2017 is shown on the pertinent maps. Background data
were screened to eliminate outliers.
One comprehensive round of sampling and analysis was conducted prior to and
reported in the August 2015 CSA. In addition, the following groundwater sampling
and analysis events have been completed:
Round 2 - September 2015 (reported in the CAP Part 1)
Round 3 - November 2015 (background wells only, reported in the CSA
Supplement 1 as part of the CAP Part 2 report)
Round 4 - December 2015 (background wells only, reported in the CSA
Supplement 1 as part of the CAP Part 2)
Round 5 – March and April 2016 (72 groundwater monitoring wells, reported in
the CSA Supplement 2)
Round 6 - May 2016
Round 7 - September 2016
Round 8 - November 2016
Round 9 - January 2017
Round 10 - April 2017
Following CAP approval but prior to final closure, an Interim Monitoring Plan (IMP)
has been proposed. The IMP is designed to supplement the compliance monitoring
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program established as part of the Site NPDES permit. The IMP is designed to monitor
near-term groundwater quality changes until the basin closure process has been
completed. Monitoring of Site groundwater monitoring wells and surface water
locations has been conducted since 2015; although, an approved IMP was not finalized
until October 2017. Agreement between NCDEQ and Duke Energy was reached on a
list of specific wells to be included in the BCSS IMP (NCDEQ, October 19, 2017) with
monitoring to begin during the third calendar quarter of 2017 and culminating in an
annual IMP report in April of the following year of monitoring. Additional details
concerning the IMP are presented in Section 14.0.
Groundwater sampling methods and the rationale for sampling locations were in
general accordance with the procedures described in the GAP (HDR, 2014). Variances
from the proposed well installation locations, methods, quantities, and well
designations are presented in Appendix G.
As described in the approved Work Plan, both unfiltered and filtered (0.45 um filter)
samples were collected for analyses of constituents whose results may be biased by the
presence of turbidity. Unless otherwise noted, concentration results discussed are for
the unfiltered samples and represent total concentrations.
Background Groundwater Concentrations 10.1
Locations for background monitoring wells installed in 2015 for the initial CSA field
effort were chosen based on the information available. The previously installed NPDES
monitoring well network provided a rudimentary groundwater water level map. Using
those maps, topographic maps, and hydrogeologic expertise, it was determined
locations northeast of the ash basin, and south of the topographic/hydrologic divide
generally along Pine Hall Road were upgradient and/or background. After the
background wells were installed and sampled a sufficient number of tables, statistical
analysis was used to confirm the analytical results represented background conditions.
The following monitoring wells have been approved by NCDEQ as background
monitoring wells (Zimmerman to Draovitch, July 7, 2017, Note: NCDEQ incorrectly
identifies MW-202D as BG-202D in the letter):
BG-2S – Shallow
BG-3S – Shallow
MW-3 – Shallow
MW-202S – Shallow
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BG-1D – Deep (transition zone)
BG-3D – Deep (transition zone)
MW-202D – Deep (transition zone)
BG-2BR-A – Bedrock
MW-202BR – Bedrock
Eight background (BG) monitoring wells BG-1S/D, BG-2S/D/BR, BG-3S/D, and MW-
202BR were proposed and installed during the 2015 CSA activities to evaluate
background water quality in the shallow (S wells), deep (D wells), and bedrock (BR
wells) flow regimes. This was in addition to the two existing NPDES background
compliance monitoring wells MW-202S and MW-202D, the Pine Hall Road Landfill
background monitoring well MW-3, the Craig Road Landfill background monitoring
well CRW-10, and the FGD Residue Landfill background monitoring wells BC-23A and
BC-28.
Evaluation of the suitability of each of these locations for background purposes was
conducted as part of the CAP 1 (Appendix H) and in technical memoranda (December
12, 2016 and May 26, 2017). Factors such as horizontal distance from the waste
boundary, the relative topographic and groundwater elevation difference compared to
the nearest ash basin surface or pore water, and the calculated groundwater flow
direction were considered to determine whether the locations represent background
conditions.
Based on these criteria, the BC-23A, BC-28, and CRW-10 locations were determined to
be installed in a different geologic environment than the ash basin. These monitoring
wells are located more than one mile southeast of the ash basin and were removed from
the background dataset. Monitoring well BG-1S has had insufficient water to sample
the well during every monitoring event and therefore is not included in the background
dataset. Elevated pH due to grout contamination negated the use of the data collected
from monitoring well BG-2BR. On March 28, 2017 monitoring well BG-2BR was
replaced with background monitoring well BG-2BR-A.
A Piper diagram, also referred to as a tri-linear diagram, is a graphical representation of
major water chemistry using two ternary plots and a diamond plot. One of the ternary
plots shows the relative percentage of major cations in individual water samples and
the other shows the relative percentage of the major anions. The apices of the cation plot
are calcium, magnesium, and sodium plus potassium. The apices of the anion plot are
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sulfate, chloride, and carbonates. The two ternary plots are projected onto the diamond
plot to represent the major ion chemistry of a water sample. The ion composition can be
used to classify groundwater of particular character and chemistry into sub-groups
known as groundwater facies. For this reason, the diamond of the piper plot is
sometimes referred to as the groundwater facies diamond. Percentages of major anions
and cations are based on concentrations expressed in meq/L (EPRI, 2006). Plots of pore
water, shallow, deep, and bedrock groundwater including background locations are
shown on Figure 10-1, Figure 10-2, and Figure 10-3.
Background Dataset Statistical Analysis 10.1.1
The revised background groundwater datasets and statistically determined
PBTVs are presented below. The current background monitoring well network
consists of wells installed within three flow zones – shallow, deep, and bedrock.
Well locations are presented on Figure 2-10.
For the bedrock groundwater dataset, less than 10 valid samples were available
for determination of PBTVs. Therefore, no formal upper tolerance limit (UTL)
statistics were run and the PBTV for the constituents in the bedrock groundwater
flow system were computed to be either:
The highest value, or
If the highest value is above an order of magnitude greater than the
geometric mean of all values, then the highest value was considered an
outlier and removed from further use and the PBTV was computed to be
the second highest value.
NCDEQ requested that the updated background groundwater dataset exclude
data from the background data set due to one or more of the following
conditions:
Sample pH is greater than or equal to 8.5 standard units (S.U.) unless the
regional NCDEQ office has determined an alternate background threshold
pH for the site;
Sample turbidity is greater than or equal to 10 Nephelometric Turbidity
Units (NTUs);
Result is a statistical outlier identified for background sample data
presented to NCDEQ on May 26, 2017;
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Sample collection occurred less than a minimum 60 days between
sampling events; and
Non-detected results are greater than 2L/IMAC.
Statistical determinations of PBTVs were performed in accordance with the
revised Statistical Methods for Developing Reference Background
Concentrations for Groundwater and Soil at Coal Ash Facilities (statistical
methods document) (HDR and SynTerra, 2017)).
Background datasets provided to NCDEQ on May 26, 2017 were revised based
on input from NCDEQ in the July 7, 2017 correspondence. The revised
background datasets for each flow system used to statistically determine
naturally occurring concentrations of inorganic constituents in groundwater are
provided in Table 10-1. The following sections summarize the refined
background datasets along with the results of the statistical evaluations for
determining PBTVs.
Shallow Flow Layer
Four monitoring wells – BG-2S, BG-3S, MW-202S, and MW-3 – monitor background
groundwater quality within the shallow flow layer. NCDEQ indicated in the July 7,
2017 letter that these shallow wells were retained for use in development of PBTVs. The
shallow flow layer dataset is presented in Table 10-1. The background groundwater
dataset meets the minimum requirement of 10 samples for all constituents. PBTVs
were calculated for constituents monitored within the shallow flow zone using formal
UTL statistics. PBTVs for the shallow flow layer are provided in Table 10-2.
Deep Flow Layer
Four monitoring wells – BG-1D, BG-2D, BG-3D, and MW-202D—monitor background
groundwater quality within the deep flow layer. NCDEQ indicated in the July 7, 2017
letter that these deep wells were retained for use in development of PBTVs. The deep
flow layer dataset is presented in Table 10-1. The background groundwater dataset
meets the minimum requirement of 10 samples for all constituents. PBTVs were
calculated for constituents monitored within the deep flow layer using formal UTL
statistics. PBTVs for the deep flow layer are presented in Table 10-2.
Bedrock Flow Layer
Two wells, BG-2BR-A and MW-202BR, monitor background groundwater quality
within the bedrock flow layer. NCDEQ indicated in the July 7, 2017 letter that these
bedrock wells were retained for use in development of PBTVs. The bedrock flow layer
dataset is presented in Table 10-1. Currently, the dataset for bedrock does not meet
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the minimum requirement of 10 samples. PBTVs for constituents in bedrock were
computed to be either the maximum value, or, if the maximum value was above an
order of magnitude greater than the geometric mean of all values, the second highest
value. PBTVs for the bedrock flow layer are presented in Table 10-2.
Summary
The calculated groundwater PBTVs were less than their applicable 2L Standards or
IMACs for all flow layers with the following exceptions:
Cobalt in the deep flow layer (PBTV of 1.6 µg/L, IMAC = 1 µg/L)
Iron in the shallow flow layer (PBTV of 750 µg/L, 2L = 300 µg/L)
Vanadium in all flow layers (shallow PBTV of 1.33 µg/L, deep PBTV of 1.45
µg/L, and bedrock PBTV 0.82 µg/L, IMAC = 0.3 µg/L)
pH in all flow layers (shallow PBTV range of 5.1 to 6.0 SU, deep PBTV range of
5.2 to 7.0 SU, bedrock PBTV range of 6.3 to 6.5 SU, 2L range = 6.5 to 8.5 SU)
Groundwater PBTVs were also calculated for the following constituents that do not
have a 2L Standard, IMAC or Federal MCL established: alkalinity, bicarbonate,
calcium, carbonate, magnesium, methane, potassium, sodium, sulfide, and total organic
carbon (TOC).
Piper Diagrams (Comparison to Background) 10.1.2
A Piper diagram, also referred to as a trilinear diagram, is a graphical
representation of major water chemistry using two ternary plots and a diamond
plot. One of the ternary plots shows the relative percentage of major cations in
individual water samples and the other shows the relative percentage of the
major anions. The apices of the cation plot are calcium, magnesium, and sodium
plus potassium. The apices of the anion plot are sulfate, chloride, and carbonates.
The two ternary plots are projected onto the diamond plot to represent the major
ion chemistry of a water sample. The ion composition can be used to classify
groundwater of particular character and chemistry into sub-groups known as
groundwater facies. For this reason, the diamond of the piper plot is sometimes
referred to as the groundwater facies diamond. Percentages of major anions and
cations are based on concentrations expressed in meq/L (EPRI, 2006). Plots of
shallow, deep, and bedrock groundwater including background locations are
shown on Figure 10-1, Figure 10-2, and Figure 10-3. All background monitoring
well locations are depicted on Figure 2-10. A generalized well construction
diagram for assessment wells is shown in Figure 10-4. Well installation
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procedures are documented in Appendix G. Boring logs and Soil Sample and
Rock Core Photographs are provided in Appendix F.
Background water types at BCSS are consistent with findings from a five year
study of groundwater flow and quality conducted at the Upper Piedmont
Research Station, located in a similar geologic setting approximately 22 miles
northeast of the Site (Huffman, et al., 2006). Samples collected from background
wells at BCSS generally indicate calcium, sodium, or potassium bicarbonate
water.
Downgradient Groundwater Concentrations 10.2
In order to best reflect current conditions at the site, the second quarter 2017
groundwater sample results are the focus for data evaluation in this report. Results
from prior events are incorporated in data evaluation and summarized as appropriate.
The second quarter 2017 data is the primary dataset used for generating
isoconcentration maps and graphical representation of data such as Piper diagrams.
Monitoring wells AB-1S, AB-2S, and AB-3S are located within the ash basin main dam.
Monitoring wells MW-101S (abandoned) and MW-102S (abandoned) are located near
the toe of the ash basin main dam. These wells are located within the ash basin waste
boundary. Monitoring well AB-9S is located within the dam at the chemical pond. The
wells are not screened within ash and are therefore not considered pore water wells;
however, due to their location within the ash basin waste boundary they are not
categorized and evaluated as downgradient wells as the constituent concentrations
reported in these wells are expected to be more representative of ash basin water than
downgradient groundwater conditions.
Groundwater isoconcentration contours with respect to each COI are depicted in
Figures 10-5 through 10-63. The isoconcentration maps present COI data in the
shallow, deep, and bedrock flow units.
Measurements of pH indicated a number of locations with pH less than the 2L lower
limit of 6.5, or higher than the 2L upper limit of 8.5. In general, elevated pH
measurements are interpreted as the result of grout contaminated wells and in
accordance with DEQ guidance, the associated groundwater samples are not used for
evaluation of constituent concentrations.
Antimony
Antimony PBTV and IMAC exceedances were not reported downgradient of the ash
basin in the shallow flow layer and are generally located at the southern end of the ash
basin. In the deep flow layer the downgradient IMAC exceedances are limited to
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beneath the southern end of the ash basin and in the vicinity of monitoring well GWA-
9D, near the southwest corner of the basin. No downgradient IMAC exceedances are
reported in the bedrock flow layer.
Arsenic
Arsenic 2L exceedances in the shallow flow layer are limited to within the footprint of
the ash basin and not downgradient. Two isolated areas exceeding the 2L standard in
the deep flow layer are located north of the ash basin main dam, one inside and one
outside of the waste boundary and within the compliance boundary. One bedrock
downgradient exceedance of arsenic is located beneath the south end of the ash basin at
AB-9BR.
Barium
One area of barium 2L exceedances was reported northwest and downgradient of the
ash basin, outside of the compliance boundary at GWA-19SA; however, no exceedances
were reported within the footprint of the basin or between the basin and the well. This
well has historical barium 2L exceedances. No barium exceedances were reported in in
the deep or bedrock flow layers.
Beryllium
Beryllium IMAC exceedances are located at and beyond the compliance boundary
northwest of and downgradient of the ash basin. Downgradient beryllium exceedances
in the deep flow layer are located north of the ash basin main dam, within the
compliance boundary at MW-103D, and northwest of the ash basin beyond the
compliance boundary at GWA-21D. No beryllium IMAC exceedances were reported in
the bedrock flow layer.
Boron
Downgradient boron exceedances of 2L in the shallow flow layer are primarily located
north of the ash basin main dam, within the compliance boundary, and northwest of the
ash basin, at or beyond the compliance boundary, and west of the structural fill at
GWA-23S. In the deep flow layer boron exceedances are located beneath the ash basin
and the Pine Hall Road Landfill, north of the ash basin main dam, within the
compliance boundary, and northwest of the ash basin, at or beyond the compliance
boundary. Boron exceedances are also reported south of the topographic divide along
Pine Hall Road, west of the structural fill. These exceedances are not related to the ash
basin and a separate assessment of the structural fill is ongoing. There are no boron
exceedances reported in the bedrock flow layer in wells that are not grout
contaminated. Monitoring wells GWA-19BR, GWA-20BR, and GWA-27BR are located
northwest of the ash basin. These wells are grout contaminated (high pH) and their
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data is not considered valid. The boron concentrations reported in these monitoring
wells are similar to the boron background concentration.
Cadmium
There are no cadmium 2L exceedances in the shallow flow layer. Downgradient
cadmium exceedances in the deep flow layer are located north of the ash basin main
dam within the compliance boundary, northwest of the ash basin at GWA-20D, located
at the compliance boundary, and at OB-9 adjacent to the Pine Hall Road Landfill.
There are no cadmium 2L exceedances reported in the bedrock flow layer.
Chloride
Downgradient chloride 2L exceedances in the shallow flow layer are located north of
the ash basin main dam within the compliance boundary, and northwest of the ash
basin, at and beyond the compliance boundary. Downgradient chloride 2L exceedances
in the deep flow layer are located beneath the north end of the ash basin and north of
the ash basin main dam within the compliance boundary, and northwest of the ash
basin, at and beyond the compliance boundary. No 2L exceedances of chloride were
reported in the bedrock flow layer.
Chromium
Downgradient 2L exceedances of chromium in the shallow flow layer are located
east/northeast of the ash basin, beyond the compliance boundary at GWA-3S, north of
the ash basin main dam, within the compliance boundary, and north/northwest of the
ash basin, beyond the compliance boundary. Downgradient exceedances in the deep
flow layer are located beneath the ash basin, west of the ash basin at GWA-16DA,
located at the compliance boundary, at GWA-11D and GWA-10DA, northwest of the
ash basin beyond the compliance boundary and at GWA-1D, located north of the ash
basin at the compliance boundary. No chromium exceedances were reported in the in
the bedrock flow layer with the exception of background monitoring well BG-2BRA.
Hexavalent Chromium
No hexavalent chromium exceedances of the 2L standard for total chromium were
reported in the shallow, deep or bedrock flow layers. Exceedances of the PBTV were
not reported in the shallow flow layer. Exceedances of the deep flow layer PBTV were
reported beneath the ash basin, and southeast and east of the ash basin, and west of the
structural fill. Exceedances of the bedrock flow layer PBTV were reported beneath the
southern end of the ash basin at AB-4BR and southwest of the ash basin at the
compliance boundary at monitoring well MW-203BR.
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Cobalt
Downgradient cobalt IMAC exceedances in the shallow flow layer are located
northeast, north, northwest, and west of the ash basin, at or beyond the compliance
boundary, and southwest of the Pine Hall Road Landfill. Exceedances of the deep flow
layer PBTV are located beneath the ash basin, and north, northwest, and west of the ash
basin, at or beyond the compliance boundary. No IMAC exceedances in the bedrock
flow layer were reported.
Iron
Downgradient exceedances of the established iron PBTV in the shallow flow layer,
which is greater than 2L, are located northeast, north, northwest, and west of the ash
basin, at or beyond the compliance boundary and west of the structural fill. Iron
exceedances of the 2L standard in the deep flow layer are located beneath the ash basin
and north, northwest, west and southeast of the ash basin, at or beyond the compliance
boundary, and west of the structural fill. There is one downgradient iron exceedances
of the 2L standard at monitoring well AB-9BR beneath the southern end of the ash
basin.
Manganese
Downgradient manganese exceedances of the 2L standard in the shallow flow layer are
located east, northeast, north, northwest, and west of the ash basin, at or beyond the
compliance boundary, and west of the structural fill. Manganese exceedances of the 2L
standard in the deep flow layer are located beneath the ash basin, east, north,
northwest, west and southeast of the ash basin, at or beyond the compliance boundary,
and west of the structural fill. Manganese downgradient exceedances in the bedrock
flow layer are located beneath the ash basin, north and southwest of the ash basin, at or
beyond the compliance boundary, and west of the structural fill.
Molybdenum
Downgradient exceedances of the molybdenum PBTV in the shallow flow layer are
located northeast of the ash basin, beyond the compliance boundary at monitoring well
GWA-3S, and north of the ash basin near the compliance boundary at GWA-1S.
Molybdenum exceedances of the PBTV in the deep flow layer are located beneath the
ash basin, northeast of the ash basin, within the compliance boundary, and northwest,
west and southeast of the ash basin, at or beyond the compliance boundary, beneath the
Pine Hall Road Landfill, and west of the structural fill. Molybdenum exceedances of the
PBTV in the bedrock flow layer are located beneath the ash basin, east, northwest, and
west, of the ash basin, at or beyond the compliance boundary, and west of the structural
fill.
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Selenium
Downgradient 2L exceedances of selenium in the shallow flow layer are located north
of the ash basin main dam, within the compliance boundary, and northwest of the ash
basin, at or beyond the compliance boundary. Exceedances of the selenium 2L standard
in the deep flow layer are limited to beneath the south end of the ash basin and beneath
the Pine Hall Road Landfill. There are no 2L exceedances of selenium in the bedrock
flow layer.
Strontium
Downgradient exceedances of the established strontium PBTV in the shallow flow layer
are located east, north, northwest, and west of the ash basin at or beyond the
compliance boundary, and west of the structural fill. Exceedances of the strontium
PBTV in the deep flow layer are located beneath the southern end and upgradient of the
ash basin and east, northeast, north, northwest, and west of the active ash basin, at or
beyond the compliance boundary, and west of the structural fill. Exceedances of the
strontium PBTV in the bedrock flow layer are located beneath the southern end of the
ash basin and east of the ash basin, within or near the compliance boundary, and north
of the ash basin beyond the compliance boundary.
Sulfate
There are no downgradient 2L exceedances of sulfate in the shallow flow layer, sulfate
exceedances are located within the basin and west of the structural fill. Sulfate 2L
exceedances in the deep flow layer are limited to beneath the south end of the ash basin,
adjacent to the Pine Hall Road Landfill, and west of the structural fill. These
exceedances are not related to the ash basin and a separate assessment of the structural
fill is ongoing. There are no sulfate 2L exceedances in the bedrock flow layer.
TDS
Downgradient 2L exceedances of TDS in the shallow flow layer are located north and
northwest of the ash basin, within or at or beyond the compliance boundary, and west
of the structural fill. TDS exceedances in the deep flow layer are located adjacent to the
Pine Hall Road Landfill and beneath the ash basin main dam, and north of the ash
basin, within the compliance boundary, northwest of the ash basin at or beyond the
compliance boundary, and west of the structural fill. These exceedances are not related
to the ash basin and a separate assessment of the structural fill is ongoing. There are no
downgradient exceedance of TDS in the bedrock flow layer.
Thallium
Downgradient exceedances of the thallium IMAC in the shallow flow layer are located
southeast, north, and northwest of the ash basin, at or beyond the compliance
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boundary. Thallium exceedances of the IMAC in the deep flow layer are located
beneath the north end of the ash basin, and north of the ash basin within the compliance
boundary, and northwest of the ash basin, at and beyond the compliance boundary.
There are no exceedances of the thallium IMAC in the bedrock flow layer.
Vanadium
No downgradient exceedances of the vanadium PBTV are located in the shallow flow
layer. PBTV exceedances are generally located within the footprint of the ash basin.
Exceedances of the PBTV in the deep flow layer are located beneath the ash basin, and
southeast, east, northeast, north, and northwest of the ash basin, at or beyond the
compliance boundary. Exceedances of the PBTV in the bedrock flow layer are located
beneath the ash basin.
Piper Diagrams (Comparison to Downgradient/ 10.2.1
Separate Flow Regime)
A 2006 EPRI study of 40 ash leachate water samples collected from 20 different
coal ash landfills and impoundments characterized bituminous coal ash leachate
as calcium-magnesium-sulfate water type and subbituminous coal ash leachate
as sodium-calcium-sulfate water type. Ash pore water at BCSS for AB-4S, AB-7S,
and AB-8S resembles bituminous coal ash leachate water from EPRI’s 2006 study
which is a calcium-magnesium-sulfate water type. In comparison, BCSS ash pore
water from AB-6S and AB-8SL have an elevated bicarbonate component.
Shallow downgradient locations characterized by calcium-magnesium-sulfate
water type include: AB-1S, AB-3S, GWA-1S, GWA-11S, GWA-20SA, and GWA-
21S . Five of these six wells indicated boron concentrations greater than 700 µg/L
for the April 2017 sampling event. GWA-31S indicates potential mixing between
background and impacted water. Downgradient location GWA-2S is
characterized as sodium-potassium-bicarbonate type indicating little influence
from source areas or a high degree of mixing with background groundwater.
Both GWA-31S and GWA-2S contained boron concentrations below the detection
limit of 50 µg/L for the April 2017 sampling event. AB-6SL, GWA-10S, GWA-
19SA, GWA-23S, GWA-30S, GWA-32S, MW-1, MW-103S, MW-104S, GWA-12S,
BG-2S, and BG-3S exhibit ion charge balance of greater than 10% (10.192% to
66.664%) and are therefore not represented on the piper diagram.
Deep groundwater locations characterized by calcium-magnesium-sulfate type
water include: AB-1D, AB-2D, AB-3D, GWA-1D, GWA-11D, GWA-20D, GWA-
21D, GWA-24D, and MW-103D. Locations that indicate potential mixing
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between background groundwater and impacted groundwater include GWA-9D
and GWA-32D. Downgradient locations GWA-2D and GWA-18D are
characterized as calcium-bicarbonate type water consistent with unimpacted
background water.
MW-200BR, MW-203BR, and BG-2BRA are characterized as calcium-bicarbonate
type water, consistent with background groundwater. No bedrock locations are
characterized as calcium-magnesium-sulfate type water.
Plots of shallow, deep, and bedrock groundwater locations are shown on Figure
10-1, Figure 10-2, and Figure 10-3. All monitoring well locations are depicted on
Figure 2-10. Boring logs and Soil Sample and Rock Core Photographs are
provided in Appendix F.
Site-Specific Exceedances (Groundwater COIs) 10.3
Site-specific COIs were developed by evaluating groundwater sampling results with
respect to PBTVs, applicable regulatory standards, and additional regulatory
input/requirements. The approach to determining those constituents which should be
considered COIs for the purpose of evaluating a site remedy is discussed in the
following section.
Provisional Background Threshold Values (PBTVs) 10.3.1
Addressing 15A NCAC 02L .0202 (b)(3) — “Where naturally occurring
substances exceed the established standard, the standard shall be the naturally
occurring concentration as determined by the Director” — HDR and SynTerra
(May 2017) provided the following report to NCDEQ: Statistical Methods for
Developing Reference Background Concentrations for Groundwater and Soil at Coal Ash
Facilities. NCDEQ (July 7, 2017) addressed each Duke Energy coal ash facility and
identified soil and groundwater data appropriate for inclusion in the statistical
analysis to determine PBTVs. A revised and updated technical memorandum
that summarized revised background groundwater datasets and statistically
determined PBTVs for BCSS was submitted to NCDEQ on August 16, 2017. A list
of NCDEQ-approved groundwater PBTVs were provided to Duke Energy on
September 1, 2017 (Zimmerman to Draovitch; Appendix A). The Proposed
Naturally Occurring (Reference Background) Concentrations In Groundwater
and Soil for BCSS (SynTerra, 2017) report is provided in Appendix H.
Applicable Standards 10.3.2
As part of CSA activities at the Site, multiple media including coal ash, ponded
water in the ash basis, ash pore water, AOWs, soil, and groundwater
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downgradient of the ash basin and in background areas have been sampled and
analyzed for inorganic constituents. Based on comparison of the sampling results
from the multiple media to applicable regulatory values, potential lists of COIs
were developed in the 2015 CSA, CAPs and CSA Supplement. For the purpose of
developing the groundwater COIs, constituent exceedances in downgradient
groundwater of PBTVs and 2L or IMAC are considered a primary focus.
Although the COI list has been developed based on site-specific conditions and
observations, certain constituents, such as boron and sulfate, may be listed as
COIs at all sites based on their usefulness as indicators of coal ash influence.
Additionally, NCDEQ requested that hexavalent chromium be included as a COI
at each CAMA-related site due to due to public interest associated with drinking
water supply wells. Molybdenum and strontium do not have 2L standards,
IMACs, or 2B standards established; however, these constituents are considered
potential contaminants of concern with regards to CCR and are evaluated as
potential COIs for the Site at the request of NCDEQ.
The following constituents do not have a 2L standard, IMAC, or Federal MCL
established: alkalinity, bicarbonate, calcium, carbonate, magnesium, methane,
potassium, sodium, sulfide, and TOC. Results from these constituents are useful
in comparing water conditions across the Site. For example calcium is listed as a
constituent for detection monitoring in Appendix III to 40 Code of Federal
Registry (CFR) Part 257. Although these constituents will be used to compare
and understand groundwater quality conditions at the site, because there are no
associated 2L standards, IMACs, or MCLs, these constituents are not evaluated
as potential COIs for the Site.
Additional Requirements 10.3.3
NCDEQ requested that figures be included in the CSA that depict groundwater
analytical results for the constituents in 40 CFR 257, Appendix III detection
monitoring and 40 CFR 257, Appendix IV assessment monitoring (USEPA CCR
Rule, 2015). Detection monitoring constituents in 40 CFR 257 Appendix III are:
Boron
Calcium
Chloride
Fluoride (limited historical data, not on assessment constituent list)
pH
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Sulfate
Total dissolved solids (TDS)
Constituents for assessment monitoring listed in 40 CFR 257 Appendix IV
include:
Antimony
Arsenic
Barium
Beryllium
Cadmium
Chromium
Cobalt
Fluoride (limited historical data, not on assessment constituent list)
Lead
Lithium (not analyzed)
Mercury
Molybdenum
Selenium
Thallium
Radium 226 and 228 combined
Aluminum, copper, iron, manganese, and sulfide were originally included in the
Appendix IV constituents in the draft rule; USEPA removed these constituents in
the final rule. Therefore, these constituents are not included in the listing above;
although, they are included as part of the current Implementation Monitoring
Plan (IMP). In addition, NCDEQ requested that vanadium be included.
BCSS Groundwater COIs 10.3.4
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Exceedances of comparative values, the distribution of constituents in relation to
the ash management areas, co-occurrence with CCR indicator constituents such
as boron and sulfate, and likely migration directions based on groundwater flow
direction are considered in determination of groundwater COIs. Based on an
evaluation of criteria described above, and based on site-specific conditions,
observations, and findings, the following list of groundwater COIs have been
initially developed for BCSS:
Antimony
Arsenic
Barium
Beryllium
Boron
Cadmium
Chloride
Chromium (total)
Chromium (hexavalent)
Cobalt
Iron
Manganese
Molybdenum
pH
Selenium
Strontium
Sulfate
Thallium
TDS
Vanadium
Table 10-3 lists the COIs at BCSS along with their associated NC 2L
Groundwater Standards, IMACs, and federal drinking water standards (Primary
Maximum Contaminant Levels [MCLs] and Secondary Maximum Contaminant
Levels [SMCLs]). NC 2L Standards are established by NCDEQ, whereas federal
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MCLs and SMCLs are established by the USEPA. Primary MCLs are legally
enforceable standards for public water supply systems set to protect human
health in drinking water. Secondary MCLs are non-enforceable guidelines set to
account for aesthetic considerations, such as taste, color, and odor (USEPA,
2014).
Water Supply Well Groundwater Concentrations and 10.4
Exceedances
Water supply well sampling results can be found in Table 4-3, provided by Duke
Energy, for the NCDENR and Duke Energy sampling results as well as identified
exceedances of 2L Standards, IMACs, and/or other regulatory limits. The analysis of
determining potential groundwater impact focuses on NCDENR results. A review of
the analytical data for the water supply wells indicated several constituents were
reported at concentrations greater than 2L or IMACs including pH (19 wells), arsenic
(six wells), chromium (one well), cobalt (one well), iron (five wells), manganese (six
wells), and vanadium (ten wells).
Concentrations of analyzed constituents exceeded their respective bedrock PBTVs for a
number of private water supply wells (data/values biased by the presence of high
turbidity are excluded) including:
Arsenic – 23 wells Barium – 18 wells
Beryllium – 1 well Cadmium – 4 wells
Calcium – 25 wells Chromium (hexavalent) – 8 wells
Chromium (total) – 1 well Copper – 19 wells
Iron – 10 wells Lead – 36 wells
Magnesium – 20 wells Manganese – 14 wells
Molybdenum – 7 wells Nickel – 1 well
Selenium – 2 wells Sodium – 1 well
Sulfate – 9 wells TDS – 10 wells
Vanadium – 10 wells Zinc – 25 wells
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11.0 HYDROGEOLOGICAL INVESTIGATION
Results of the hydrological investigation summarized in this section are primary
components of the Site Conceptual Model.2 Plume physical and chemical
characterization is detailed below for each groundwater COI. The horizontal and
vertical extent of constituent concentrations is presented on isoconcentration maps and
cross sections. These descriptions are primarily based on the most recent groundwater
sampling event (April 2017).
Plume Physical Characterization 11.1
Boron is the primary CCR-derived constituent in groundwater and is detected at
concentrations greater than the NC 2L standard beneath the ash basin and the Pine Hall
Road Landfill and downgradient of the ash basin (north and northwest). Boron is not
detected in background groundwater. Boron, in its most common forms, is soluble in
water, and boron has a very low Kd value, making the constituent highly mobile in
groundwater. Therefore, the presence/absence of boron in groundwater provides a
close approximation of the distribution of CCR-impacted groundwater. The detection
of boron at concentrations in groundwater greater than applicable 2L standards and
PBTVs best represents the leading edge of the CCR-derived plume moving
downgradient from the source area (ash basin and Pine Hall Road Landfill).
The groundwater plume is defined as any locations (in three-dimensional space) where
groundwater quality is impacted by the ash basin. Other COIs (defined in Section 10.0)
are used to help refine the extent and degree to which areas are impacted by
groundwater from the ash basin. The comprehensive groundwater data table
(Appendix B, Table 1) and an understanding of groundwater flow dynamics and
direction (Section 6.3, Figure 6-6 to 6-11) were used to define the horizontal and vertical
extent of the plume. As discussed in Section 13.2 (Geochemical Modeling), not all
constituents with PBTV exceedances can be attributed to the ash basin. Naturally
occurring groundwater contains varying concentrations of alkalinity, aluminum,
bicarbonate, cadmium, carbonate, copper, lead, magnesium, methane, nickel,
potassium, sodium, total organic carbon (TOC), and zinc. Sporadic and low-
2 Pursuant to the CCR rule, owners and operators of CCR units must install the required groundwater monitoring
system; develop the required groundwater sampling and analysis program to include selection of the statistical
procedures to be used for evaluating groundwater monitoring data; and begin detection monitoring, which requires
owners and operators to have a minimum of eight samples for each well and begin evaluating groundwater
monitoring data for statistically significant increases over background levels for the constituents listed in Appendix III
of 40 C.F.R. Part 257. These data need not be posted to Duke Energy’s publicly accessible Internet site until such
time the annual groundwater monitoring and corrective action report required under the CCR rule becomes
due. Although a portion of these data was utilized in this assessment for refinement of constituent distribution, these
data are not included in this report because it was not public information as of the date of its completion.
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concentration exceedances of these constituents in the groundwater data do not
necessarily demonstrate horizontal or vertical distribution in groundwater that
indicates impact from the ash basin.
The horizontal extent of the plume in each flow layer is depicted in concentration
isopleth maps (Figure 10-5 to 10-63). These maps use groundwater analytical data to
spatially and visually define areas where groundwater concentrations are above the
respective constituent PBTV and/or 2L/IMAC. The leading edge of the plume, the
farthest downgradient edge, is represented by groundwater concentrations in the wells
in each flow layer. In the bedrock flow layer, boron is reported in downgradient well
MW-200BR, located north of the ash basin main dam at the compliance boundary at a
concentration greater than the PBTV and less than the 2L standard. Boron is also
detected in the bedrock flow layer at monitoring well GWA-20BR, located northwest of
the ash basin at a concentration similar to the PBTV and less than the 2L standard.
Boron is also detected in the bedrock flow layer at monitoring well OB-9, located
north/northwest of the Pine Hall Road Landfill at a concentration greater than the PBTV
and less than the 2L standard. The leading edge of the bedrock boron plume is
interpreted to be at or just beyond these monitoring wells. The remaining bedrock
downgradient wells did not have boron detected. In the deep flow layer, boron results
in the monitoring wells located within the compliance boundary on the east and
southeast sides of the ash basin are non-detect. On the north side of the ash basin,
boron is reported in downgradient well MW-200D, located north of the ash basin main
dam at the compliance boundary at a concentration greater than the PBTV and less than
the 2L standard. Northwest of the ash basin, boron is reported at a concentration
greater than the 2L standard at monitoring well GWA-27D located beyond the
compliance boundary. Monitoring wells installed for other regulatory programs have
added additional details about the orientation and extent of the downgradient plume
and have helped refine an understanding of the distribution of the plume. The boron
concentrations reported in monitoring wells GWA-10DA, GWA-31D, and GWA-30D
are non-detect. These wells are located beyond GWA-21D and the leading edge of the
boron plume is expected to be generally between GWA-27D and this set of wells. Boron
results exceed the 2L standard beneath the Pine Hall Road Landfill in the deep flow
layer, but are non-detect at the compliance boundary. The leading edge of the boron
plume in the shallow flow layer east of the ash basin is generally at the compliance
boundary. North of the ash basin main dam and northwest of the ash basin, the boron
plume in the shallow flow layer extends to beyond the compliance boundary. The
boron concentration is non-detect in monitoring wells GWA-30S and GWA-31S which
define the leading edge of the boron plume in the shallow flow layer. West of the ash
basin the boron concentrations are non-detect or less than the PBTV at the compliance
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boundary. As described in Section 6.0, there is no hydrogeologic confining unit at
BCSS; therefore, under these unconfined conditions, groundwater moves freely across
each layer shown in a vertical gradient map (Figure 6-12).
Figures 11-1 through 11-3 depict concentration versus distance from the source along
the plume centerline for COIs. Concentrations of each COI were measured from
sampling in April-May 2017. The wells used are consistent for each constituent
represented. Within the source area, well AB-4S was used for the shallow flow layer,
well AB-4D was used for the deep flow layer, and well AB-4BR was used for the
bedrock flow layer. At the compliance boundary, downgradient of the ash basin main
dam, GWA-1S was used for the shallow flow layer, MW-200D was used for the deep
flow layer, and MW-200BR was used in the bedrock flow layer. The wells at or beyond
the compliance boundary downgradient of the ash basin main dam are MW-200S for
the shallow flow layer, GWA-24D for the deep flow layer, and GWA-24BR for the
bedrock flow layer. While PBTV values could not be distinguished on these graphs
because values differ by flow unit, the graphs show constituent concentrations in source
areas and downgradient and aid in understanding plume distribution.
The vertical extent of the plume extent is depicted in the cross-sectional views of the site
(Figures 6-2 and 11-4 to 11-63). Cross-section A-A’ is a transect of the ash basin and the
plume, along the plume centerline, from south to north. There are 29 CAMA wells, 2
geotechnical borings, and two wells from other regulatory programs along the
centerline. These wells represent background, source area, and downgradient locations
relative to the ash basin. Cross-section B-B’ is a transect perpendicular to the plume
centerline. There are 25 CAMA wells and 3 geotechnical borings along the transect.
These wells are background, source area, downgradient, and sidegradient locations
relative to the ash basin. Cross-section C-C’ is a transect parallel to Middleton Loop
Road requested by DEQ. There are 29 CAMA wells and 3 wells from other regulatory
programs along the transect.
The well screens in the CAMA wells accurately monitor groundwater conditions and
impact to the shallow and deep flow layers. Likewise, as has been demonstrated with
the installation of deeper bedrock well AB-4BRD beneath the ash basin (AB-9BRD is
grout contaminated and the data is not usable), impact to the bedrock flow unit is
confined to the top approximately 100-140 feet of fractured bedrock.
The vertical extent of the plume is best represented by groundwater concentrations in
bedrock wells beneath and downgradient of the ash basin. Boron is present in the
saprolite beneath the ash basin, extending into the bedrock beneath the ash basin main
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dam. Boron concentrations are less than the 2L standard approximately 300 feet
downgradient of the toe of the ash basin main dam, prior to the MW-200 well nest.
As groundwater under the ash basin flows north toward the ash basin dam, the
hydraulic impact of the ash basin dam and the hydraulic head exerted by the ash basin
water, forces groundwater downward into the bedrock, which increases hydraulic
pressure in the bedrock aquifer. In general, the pressures in the bedrock just
downgradient of the base of the dam become greater than in the transition zone or
surficial aquifers as indicated by the artesian conditions encountered at monitoring well
MW-200BR located along the designated effluent channel. Groundwater elevations are
not available to calculate vertical gradients in the well clusters installed near and along
the base of the dam. A downward gradient exists to the east and west of the designated
effluent channel downgradient of the dam. As groundwater and the plume migrate in
the downgradient direction, unimpacted groundwater enters the system from
upgradient recharge areas to the west and east, mitigating the concentration of some
COIs (e.g., boron).
The horizontal and vertical extent of the plume has been defined. Further, it can be
concluded that monitoring wells across the site are appropriately placed and screened
to the correct elevations to monitor groundwater quality. Monitoring wells installed for
other regulatory programs have added additional details about the orientation and
extent of the downgradient plume and have helped refine an understanding of the
vertical and horizontal distribution of the plume.
Plume Chemical Characterization 11.2
Plume chemical characterization is detailed below for each COI. Analytical results are
based on the April 2017 groundwater sampling event. The range of detected
concentrations is presented with the number of detections for the sampling event.
Descriptions of the COIs identified for BCSS are also provided. Samples that have
turbidity >10 NTUs or pH greater than 9.0 (indicative of grout contamination in the
well) have been removed from the data set.
Antimony
Reported Range: 0.1 µg/L – 26.2 µg/L; Number of Detections/Total Samples:
33/94
Concentrations in 12 samples exceeded the PBTV. Concentrations in 7
samples exceeded the IMAC.
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Antimony exceeds the PBTV and IMAC in ash basin pore water
groundwater beneath the ash basin, transition zone downgradient of the
ash basin.
Antimony is a silvery-white, brittle metal. In nature, antimony combines with
other elements to form antimony compounds. Small amounts of antimony are
naturally present in rocks, soils, water, and underwater sediments. Only a few
ores of antimony have been encountered in North Carolina. Antimony has been
found in combination with other metals, and is found most commonly in
Cabarrus County and other areas of the Carolina Slate Belt (Chapman, Cravotta,
III, Szabo, & Lindsey, 2013). In a USGS study of naturally occurring trace
minerals in North Carolina, 57 private water supply wells were sampled to
obtain trace mineral data. Of the wells sampled, no wells contained antimony
above the USEPA primary MCL (Chapman, Cravotta, III, Szabo, & Lindsey,
2013). Antimony is compared to an IMAC since no 2L Standard has been
established for this constituent by NCDEQ.
Arsenic
Reported Range: 0.041 µg/L – 227 µg/L; Number of Detections/Total Samples:
83/94
Concentrations in 36 samples exceeded the PBTV. Concentrations in 12
samples exceeded the 2L.
Arsenic exceeds the PBTV and 2L in pore water, transition zone and
bedrock groundwater beneath the ash basin and downgradient shallow
and bedrock groundwater.
Arsenic soil concentrations from 52 samples beneath the ash basin and
downgradient of the ash basin exceed the PSRG for POG value; 35
samples exceed the PBTV.
Arsenic is a trace element in the crust, with estimated concentrations ranging
from less than one mg/kg in mafic igneous rocks to 13 mg/kg in clay rich rocks
(Parker, 1967). It occurs in multiple valence states (As5+, As3+, and As3-). Arsenic in
coal occurs primarily in pyrite (iron sulfide, with arsenic replacing iron in the
crystal structure) (Finkelman, 1995). Arsenic condenses on fly ash as arsenate
(As5+) (Goodarzi, Huggins, & Sanei, 2008). Leaching tests on ash indicate that
trace quantities up to 50 percent of the arsenic present can be leached. In addition
to the solubility of the source, the concentration of calcium and presence of
oxides appear to limit the mobility of arsenic (Izquierdo & Querol, 2012). The
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USEPA estimates that the amount of natural arsenic released into the air as dust
from the soil is approximately equal to the amount of arsenic released by all
human activities (EPRI, 2008b).
Barium
Reported Range: 0.918 µg/L – 746 µg/L; Number of Detections/Total Samples:
89/94
Concentrations in 63 samples exceeded the PBTV. Concentrations in 1
sample exceeded the 2L in downgradient shallow groundwater.
Barium exceeds the PBTV in all flow units beneath the ash basin and
downgradient of the ash basin.
Barium is a naturally occurring component of minerals that are found in small,
but widely distributed amounts in the earth’s crust (Kunesh, 1978); (Miner, 1969).
Two forms of barium, barium sulfate (barite) and barium carbonate (witherite),
are often found in nature as ore deposits. Barium enters the environment
naturally through the weathering of rocks and minerals. Anthropogenic releases
are primarily associated with industrial processes.
Barium is sometimes found naturally in drinking water and food. However,
because the dominant naturally occurring barium compounds (barium sulfate
and barium carbonate) have a low to moderate solubility in water under most
conditions, the amount of barium found in drinking water is typically small.
Barium compounds such as barium acetate, barium chloride, barium hydroxide,
barium nitrate, and barium sulfide dissolve more easily in water than barium
sulfate and barium carbonate, but because they are not commonly found in
nature, they do not usually occur in drinking water unless the water is
contaminated by barium compounds that are released from waste sites (EPRI,
2008b).
Barium is naturally released into the air by soils as they erode and is released
into the soil and water by eroding rocks. Barium released into the air by human
activities comes mainly from barium mines, metal production facilities, and
industrial boilers that burn coal and oil (EPRI, 2008b). The leachability of barium
has been found to be relatively independent of pH but is controlled instead by
the presence of calcium with which it competes for sulfate (Fruchter et al., 1990).
In an overview of leachability studies found in the International Journal of Coal
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Geology, the mobility of barium typically ranged from 0.02 to 2 percent (Izquierdo
& Querol, 2012).
Regional metamorphic grade greenschist to upper amphibolite in the Piedmont’s
King’s Mountain Belt contains deposits of barium sulfate (barite). Barium is
especially common as concretions and vein fillings in limestone and dolostone,
which are not common geologic facies in North Carolina; however, at various
times in the past century and a half, the Carolinas have been major producers of
barite (USEPA, 2014).
In a statistical summary of groundwater quality in North Carolina, the
Superfund Research Program at the University of North Carolina (UNC)
analyzed 1,898 private well water samples in Gaston and Mecklenburg Counties.
The samples were tested by the North Carolina State Laboratory of Public Health
from 1998-2012. This study found an average barium concentration of 50 µg/L.
No samples exceeded the 2,000 µg/L Primary Maximum Contaminant Level
(PMCL) for barium (NC DHHS, 2010).
Beryllium
Reported Range: 0.012 µg/L – 11.5 µg/L; Number of Detections/Total Samples:
69/94
Concentrations in 16 samples exceeded the PBTV. Concentrations in 7
samples exceeded the IMAC.
Beryllium exceeds the PBTV and 2L in pore water and transition zone
groundwater beneath the ash basin.
Beryllium detected in groundwater in all three flow units downgradient of
the ash basin including exceedance of PBTV and 2L in surficial and
transition zone groundwater.
Beryllium is a hard, gray metal that is very lightweight. In nature, it combines
with other elements to form beryllium compounds. Small amounts of these
compounds are naturally present in soils, rocks, and water. Emeralds and
aquamarines are gem-quality examples of a mineral (beryl) that is a beryllium
compound.
Beryllium combines with other metals to form mixtures called alloys. Beryllium
and its alloys are used to construct lightweight aircraft, missile, and satellite
components. Beryllium is also used in nuclear reactors and weapons, X-ray
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transmission windows, heat shields for spacecraft, rocket fuel, aircraft brakes,
bicycle frames, precision mirrors, ceramics, and electrical switches (EPRI, 2008c).
Most of the beryl occurring in North Carolina is along the south and southwest
sides of the Blue Ridge Mountains. The most notable mines include the
Biggerstaff, Branchand, and Poteat mines in Mitchell County; the Old Black mine
in Avery County; and the Ray mine in Yancey County. The beryl forms golden or
pale-green well-formed prismatic crystals ranging in size from a fraction of an
inch to about 3 inches in diameter. It is generally found near the cores of bodies
of pegmatites of moderate size that contain considerable amounts of perthitic
microcline. Production has been negligible, and no regular production appears
possible. Green beryl (aquamarine and emerald) was mined commercially many
years ago at the Grassy Creek emerald mine and the Grindstaff emerald mine on
Crabtree Mountain in Mitchell County. The Ray mine in Yancey County has also
produced some golden beryl and aquamarine (Brobst, 1962). Beryllium-
containing minerals are also common in granites and pegmatites throughout the
Piedmont; however, to a lesser degree than the Blue Ridge Mountains Province
(Brobst, 1962).
Beryllium is concentrated in silicate minerals relative to sulfides and in feldspar
minerals relative to ferromagnesium minerals. The greatest known naturally
occurring concentrations of beryllium are found in certain pegmatite bodies.
Beryllium is not likely to be found in natural water above trace levels due to the
insolubility of oxides and hydroxides at the normal pH range (Brobst, 1962). In
groundwater, beryllium concentrations are compared to IMAC since no 2L
Standard has been established for this constituent by NCDEQ.
Boron
Reported Range: 25.3 µg/L – 26,700 µg/L; Number of Detections/Total Samples:
53/94
Concentrations in 38 samples exceeded the PBTV. Concentrations in 23
samples exceeded the 2L.
Boron exceeds the PBTV and 2L in pore water and transition zone
groundwater beneath the ash basin.
Boron detected in groundwater in all three flow units downgradient of the
ash basin including exceedance of PBTV and 2L in surficial and transition
zone groundwater.
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Soil concentrations beneath the ash basin exceed the PBTV and PSRG for
POG value.
Boron is a trace element in the crust, with estimated concentrations ranging from
as little as 1 mg/kg in mafic igneous rocks to hundreds of milligrams per
kilogram in clay rich rocks (Parker, 1967). It occurs only in the trivalent form
(B3+) and is concentrated in sedimentary rocks (Urey & Mem, 1953). This
observation indicates that a mechanism exists to concentrate boron in minerals
because the oceans could dissolve all of the boron estimated to be present in the
crust (Fleet, 1965). Fleet (1965) presents both biogenic and mineralogical
processes to account for the preferential concentration of boron in the crust.
Boron is a micronutrient (Goldberg, 1997) that is concentrated in plant tissue,
including the plants from which coal formed.
While boron is relatively abundant on the earth’s surface, boron and boron
compounds are relatively rare in all geological provinces of North Carolina.
Natural sources of boron in the environment include volatilization from
seawater, geothermal vents, and weathering of clay-rich sedimentary rocks.
Total contributions from anthropogenic sources are less than contributions from
natural sources. Anthropogenic sources of boron include agriculture, refuse, coal
and oil burning power plants, by-products of glass manufacturing, and sewage
and sludge disposal (EPRI, 2005)).
Because boron is associated with the carbon (fuel) in coal, it tends to volatilize
during combustion and subsequently condense onto fly ash as a soluble borate
salt (Dudas, 1981). Boron leaches readily (up to 50 percent of total present) and
rapidly from fly ash (Cox, Lundquist, Przyjazny, & Schmulbach, 1978). Boron is
considered a marker COI for coal ash because boron is rarely associated with
other types of industrial waste products.
Boron is the primary component of a few minerals including tourmaline, a rare
gem mineral that forms under high temperature and pressure (Hurlbut, 1971).
The remaining common boron minerals, including borax that was mined for
laundry detergent in Death Valley, California, form from the evaporation of
seawater in deposits known as evaporites. For this reason, boron mobilized into
the environment will remain in solution until incorporation into plant tissue or
adsorption by a mineral.
Fleet describes sorption of boron by clays as a two-step process. Boron in
solution is likely to be in the form of the borate ion (B(OH)4-). The initial
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sorption occurs onto a charged surface. Observations that boron does not tend to
desorb from clays indicates that it migrates rapidly into the crystal structure,
most likely in substitution for aluminum. Goldberg et al. (1996) determined that
boron sorption sites on clays appear to be specific to boron. For this reason, there
is no need to correct for competition for sorption sites by other anions in
transport models.
Goldberg (1997) lists aluminum and iron oxides, magnesium hydroxide, clay
minerals, calcium carbonate (limestone), and organic matter as important
sorption surfaces in soils. Boron sorption on oxides is diminished by competition
from numerous anions. Boron solubility in groundwater is controlled by
adsorption reactions rather than by mineral solubility. Goldberg concludes that
chemical models can effectively replicate boron adsorption data over changing
conditions of boron concentration, pH, and ionic strength.
Cadmium
Reported Range: 0.051 µg/L – 3.3 µg/L; Number of Detections/Total Samples:
29/94
Concentrations in 6 samples exceeded the PBTV. Concentrations in 2
samples exceeded the 2L in the transition zone downgradient of the ash
basin.
Historic detections show concentrations increasing for pore water beneath
the ash basin.
Historic detections are stable for the two locations that exceed the 2L.
Cadmium is generally characterized as a soft, ductile, silver-white or bluish-
white metal, and is listed as 64th in relative abundance amongst the naturally
occurring elements. Cadmium is found principally in association with zinc
sulfide based ores and, to a lesser degree, as an impurity in lead and copper ores.
It is also found in sedimentary rocks at higher levels than in igneous or
metamorphic rocks, with the exception of the nonferrous metallic ores of zinc,
lead and copper (WHO 2011). Cadmium often co-occurs with zinc minerals like
sphalerite, and can substitute in the sphalerite crystal structure during
weathering (USGS 1985).
Cadmium is found throughout the environment from natural sources and
processes such as the erosion and abrasion of rocks and soils and from singular
events such as forest fires and volcanic eruptions (USGS 1985).
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Cadmium occurs sporadically in the auriferous parts of the North Carolina
Charlotte and Carolina Slate Belts. Cadmium is widespread in the Carolina Slate
Belt, but is found in the Charlotte Belt only near its southeastern boundary. A
cluster of cadmium sites marks the mineralized district in the northeast corner of
the Carolina Slate Belt, where cadmium was found in all zinc-rich samples.
The solubility of cadmium in water is influenced to a large degree by its acidity;
suspended or sediment-bound cadmium may dissolve when there is an increase
in acidity. In natural waters, cadmium is found mainly in bottom sediments and
suspended particles (WHO 2011).
Contamination of drinking water may occur as a result of the presence of
cadmium as an impurity in the zinc of galvanized pipes or cadmium-containing
solders in fittings, water heaters, water coolers and taps. Levels of cadmium
could be higher in areas supplied with soft water of low pH, as this would tend
to be more corrosive in plumbing systems containing cadmium. Cadmium is
used in battery production, dye and pigment manufacturing, coatings and
plating, as a stabilizing agent in plastic production, nonferrous alloys, and
photovoltaic devices (WHO 2011).
In a statistical summary of groundwater quality in North Carolina, the
Superfund Research Program at UNC analyzed private well water samples
tested by the North Carolina State Laboratory of Public Health from 1998-2010.
Summary statistics for the 399 wells tested in Stokes and Rockingham counties
are included in Table 11-1. The average cadmium concentrations were 0.5 µg/L
and 0.6 µg/L in Stokes and Rockingham counties, respectively.
Chloride
Reported Range: 0.67 µg/L – 884 µg/L; Number of Detections/Total Samples:
94/94
Concentration in 32 samples exceeds the PBTV. Concentrations in 11
samples exceeded the 2L.
Exceedances of 2L occur in the pore water and transition zone beneath the
ash and shallow and transition zone groundwater downgradient of the
ash basin.
Historic detections are show stable or decreasing concentrations and
include some exceedances of PBTVs in surficial, transition zone and
bedrock groundwater downgradient of the ash basin.
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Chloride is a major ion, and occurs widely as a salt of sodium (NaCl), potassium
(KCl), and calcium (CaCl2). Oceans typically contain about 19,000 mg/L of
chloride (Feth 1981). Elevated levels of chloride may occur in groundwater as a
result of sea water intrusion, or erosion of halite (U.S. Geological Survey, 2009).
The USEPA has not established an MCL for chloride because it is not known to
have adverse effects on human health. An SMCL of 250 mg/L has been
established for chloride because of taste and corrosive considerations. The taste
threshold for chloride depends on the associated cation. A study by Lockhart
(1955) found that people detected a salty taste in water at 210, 310, and 222 mg/L
from the respective sodium, potassium, and calcium salts. The taste of coffee is
affected when brewed with water containing chloride concentrations ranging
from 400-530 mg/L, depending on the corresponding cation (Lockhart 1955).
Chloride concentrations above 250 mg/L in drinking water may cause corrosion
in water distribution systems (McConnell & Lewis, 1972).
Using the USGS National Uranium Resource Evaluation (NURE) database, all
chloride groundwater test results within a 20-mile radius of the BCSS site are
shown on Figure 11-64. These samples were taken at depths ranging from 20 to
500 ft bgs, and the chloride concentrations range from below detection limits to
55.7 mg/L.
Chromium
Reported Range: 0.098 µg/L – 289 µg/L; Number of Detections/Total Samples:
79/94
Concentrations in 14 samples exceeded the PBTV. Concentrations in 7
samples exceeded the 2L in the shallow and transition zone downgradient
of the ash basin, and at one background location.
Historic detections are inconsistent but include some 2L exceedances and
in surficial and transition zone groundwater downgradient of the ash
basin.
Chromium soil concentrations from 79 samples beneath the ash basin and
downgradient of the ash basin exceed the PSRG for POG value, only 13
samples exceed the PBTV.
Chromium is a blue-white metal found naturally occurring in combination with
other substances. It occurs in rocks, soils, plants, and volcanic dust and gases
(EPRI, 2008a). Background concentrations of chromium in groundwater
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generally vary according to the media in which they occur. Most chromium
concentrations in groundwater are low averaging less than 1.0 µg/L worldwide.
Chromium tends to occur in higher concentrations in felsic igneous rocks (such
as granite and metagranite) and ultramafic igneous rocks; however, it is not a
major component of the igneous or metamorphic rocks found in the North
Carolina Piedmont or the Blue Ridge (Chapman, Cravotta, III, Szabo, & Lindsey,
2013).
In a statistical summary of groundwater quality in North Carolina, the
Superfund Research Program at UNC analyzed 1,898 private well water samples
in Gaston and Mecklenburg Counties. The samples were tested by the North
Carolina State Laboratory of Public Health from 1998 to 2012. The average
chromium concentrations were 5.1µg/L and 5.2µg/L in Gaston and Mecklenburg
Counties respectively.
Hexavalent Chromium
Reported Range: 0.0092 µg/L – 8.3µg/L; Number of Detections/Total Samples:
56/94
Concentrations in 14 samples exceeded the PBTV.
Hexavalent chromium exceeds the PBTV in transition zone and bedrock
groundwater beneath the ash basin;
Hexavalent chromium exceeds the PBTV in transition zone groundwater
upgradient and sidegradient of the ash basin; and bedrock groundwater
downgradient.
Hexavalent chromium exceeds the PBTV in transition zone in
groundwater south of the ash basin’s topographic ridge, west of the
structural fill.
Historic detections are inconsistent but include some PBTV exceedances
and in the transition zone groundwater beneath the ash basin and
sidegradient and downgradient of the ash basin.
Chromium can also occur in the +III oxidation state, depending on pH and redox
conditions. Cr (VI) is the dominant form of chromium in shallow aquifers where
aerobic conditions exist. Cr(VI) can be reduced to Cr(III) by soil organic matter,
S2- and Fe2+ ions under anaerobic conditions often encountered in deeper
groundwater. Major Cr(VI) species include chromate (CrO42-) and dichromate
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(Cr2O72-) which precipitate readily in the presence of metal cations (especially
Ba2+, Pb2+, and Ag+). Chromate and dichromate also adsorb on soil surfaces,
especially iron and aluminum oxides. Cr(III) is the dominant form of chromium
at low pH.
Chromium mobility depends on sorption characteristics of the soil, including
clay content, iron oxide content and the amount of organic matter present.
Chromium can be transported by surface runoff to surface waters in its soluble
or precipitated form. Soluble and unadsorbed chromium complexes can leach
from soil into groundwater. The leachability of Cr(VI) increases as soil pH
increases. Most of chromium released into natural waters is particle associated,
however, and is ultimately deposited into the sediment (Smith et al., 1995).
Cobalt
Reported Range: 0.019 µg/L – 85.6 µg/L; Number of Detections/Total Samples:
83/94
Concentrations in 31 samples exceeded the PBTV. Concentrations in 32
samples exceeded the IMAC.
Three samples above IMAC in the transition zone are below the PBTV
Cobalt exceeds the PBTV and IMAC in pore water and transition zone
groundwater beneath the ash basin.
Cobalt exceeds the PBTV and IMAC in shallow and transition zone
groundwater downgradient of the ash basin.
Historic detections generally show decreasing concentrations overtime
except at locations northwest of the ash basin.
Soil concentrations beneath the ash basin and downgradient of the ash
basin exceed the PSRG for POG value but only one location (SB-03)
exceeds the PBTV.
Cobalt is a base metal that exhibits geochemical properties similar to iron and
manganese, occurring as a divalent and trivalent ion. Cobalt can also occur as
Co-1. In terms of distribution in the crust, all three metals exhibit a strong affinity
for mafic igneous and volcanic rocks and deep-sea clays (Parker, 1967). Cobalt
occurs in clay minerals and substitutes into the pyrite crystal structure. There is
also evidence that it is organically bound in coal (Finkelman, 1995). Izquierdo
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and Querol (2012) report limited leaching of cobalt from coal, attributing this
observation to incorporation into iron oxide minerals. The concentration of cobalt
in surface and groundwater in the United States is generally low— between 1
and 10 parts of cobalt in 1 billion parts of water (ppb) in populated areas. The
concentration may be hundreds or thousands times higher in areas that are rich
in cobalt containing minerals or in areas near mining or smelting operations. In
most drinking water, cobalt levels are less than 1 to 2 ppb (U.S. Geological
Survey, 1973). Cobalt is compared to IMAC since no 2L standard has been
established for this constituent by NCDEQ.
Iron
Reported Range: 1.91 µg/L – 88,300 µg/L; Number of Detections/Total Samples:
83/94
Concentrations in 24 samples exceeded the PBTV. Concentrations in 38
samples exceeded the 2L.
Iron exceeds the PBTV and 2L in pore water, transition zone, and bedrock
groundwater beneath the ash basin.
Iron detected in groundwater downgradient of the ash basin including
exceedances of PBTV and 2L in shallow and transition zone groundwater.
All 119 soil samples concentrations beneath the ash basin and
downgradient of the ash basin exceed the PSRG for POG value but only 9
locations exceeds the PBTV.
Iron is a naturally occurring element that may be present in groundwater from
the erosion of natural deposits (NC DHHS, 2010). A 2015 study by DENR
(Summary of North Carolina Surface Water Quality Standards 2007-2014) found
that while concentrations vary regionally, “iron occurs naturally at significant
concentrations in the groundwaters of NC,” with a statewide average
concentration of 1,320 µg/L. Iron is estimated to be the fourth most abundant
element in the Earth’s crust at approximately five percent by weight (Parker,
1967). Only Oxygen (46.60 weight percent), silicon (27.72 weight percent), and
aluminum (8.13 weight percent) occur in higher concentrations. Iron occurs in
divalent (ferrous, Fe2+), trivalent (ferric, Fe+3), hexavalent (Fe6+), and Fe2- oxidation
states. Iron is a common mineral forming element, occurring primarily in mafic
(dark colored) minerals including micas, pyrite (iron disulfide), and hematite
(iron oxide), as well as in reddish-colored clay minerals.
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Clay minerals and pyrite are common impurities in coal. Under combustion
conditions in a coal-fired boiler, clay minerals would be dehydrated to mullite or
gibbsite, possibly liberating iron, and pyrite would oxidize to hematite or
magnesioferrite. Research summarized by Izquierdo and Querol (2012) indicates
that iron leaching from coal ash is on the order of 1 percent of the total iron
present due to the low pH required to solubilize iron minerals. Despite the low
apparent mobilization percentage, iron is often one of the COIs detected in the
highest concentrations in ash pore water. Ferric iron is soluble at pH less than 2
at typical surface conditions (25°C and 1 atmosphere total pressure, Schmitt,
1962). For this reason, dissolved iron in surficial waters is typically oxidized to
the trivalent state resulting in formation of ferric iron oxide flocculation that
exhibits a characteristic reddish tint.
Manganese
Reported Range: 1.73 µg/L – 11,600 µg/L; Number of Detections/Total Samples:
89/94
Concentrations in 61 samples exceeded the PBTV. Concentrations in 47
samples exceeded the 2L.
Manganese exceeds the PBTV and 2L in pore water, transition zone, and
bedrock groundwater beneath the ash basin.
Manganese detected in groundwater downgradient of the ash basin
including exceedances of PBTV and 2L in shallow, transition zone and
bedrock groundwater.
Historic detections generally show decreasing concentrations overtime for
each flow layer except at locations northwest of the ash basin.
Manganese concentrations from 98 soil samples concentrations beneath
the ash basin and downgradient of the ash basin exceed the PSRG for
POG value but no samples exceed the PBTV.
Manganese is a naturally occurring silvery-gray transition metal that resembles
iron, but is more brittle and is not magnetic. It is found in combination with iron,
oxygen, sulfur, or chlorine to form manganese compounds. High manganese
concentrations are associated with silty soils, and sedimentary, unconsolidated,
or weathered lithologic unit and low concentrations are associated with non-
weathered igneous bedrock and soils with high hydraulic conductivity
(Gillespie, 2013), (Polizzotto, et al., 2015). Manganese is most readily released to
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the groundwater through the weathering of mafic or siliceous rocks (Gillespie,
2013). When manganese-bearing minerals in saprolite, such as biotite, are
exposed to acidic weathering, the metal can be liberated from the host mineral
and released to groundwater. It then migrates through pre-existing fractures
during the movement of groundwater through bedrock. If this aqueous-phase
manganese is exposed to higher pH in the groundwater system, it will
precipitate out of solution. This results in preferential pathways becoming
“coated” in manganese oxides and introduces a concentrated source of
manganese into groundwater (Gillespie, 2013). Manganese(II) in suspension of
silt or clay is commonly oxidized by microorganisms present in soil, leading to
the precipitation of manganese minerals (ATSDR, 2012). Roughly 40-50% of
North Carolina wells have manganese concentrations higher than the state
drinking water standard (Gillespie, 2013). Concentrations are spatially variable
throughout the state, ranging from less than 0.01 mg/L to more than 2 mg/L. This
range of values reflects naturally derived concentrations of the constituent and is
largely dependent on the bedrock’s mineralogy and extent of weathering
(Gillespie, 2013).
Manganese is estimated to be the twelfth most abundant element in the crust
(0.100 weight percent, (Parker, 1967). Manganese exhibits geochemical properties
similar to iron with Mn7+, Mn6+, Mn4+, Mn3+, Mn2+, and Mn1- oxidation states.
Manganese substitutes for iron in many minerals. Similar to iron, manganese
leaching from coal ash is limited to less than 10 percent of the total manganese
present due to the low pH required to solubilize manganese minerals (Izquierdo
& Querol, 2012). Despite the low apparent mobilization percentage, manganese
can be detected in relatively high concentrations in ash pore water.
Molybdenum
Reported Range: 0.12 µg/L – 3,460 µg/L; Number of Detections/Total Samples:
59/94
Concentrations in 25 samples exceeded the PBTV.
Molybdenum exceeds the PBTV in pore water, transition zone and
bedrock groundwater beneath the ash basin.
Molybdenum detected in groundwater downgradient of the ash basin
including exceedances of PBTV in shallow, transition zone and bedrock
groundwater.
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Molybdenum is a trace element that exists predominantly as Mo(IV) and Mo(VI).
As a free metal, it is silvery gray, although it does not occur in this form in
nature. It is mined for use in alloys. Mo commonly forms oxyanions in
groundwater that are affected by redox and pH (Ayotte, Gronbert, & Apodaca,
2011). Mo has been observed to leach less from coal cleaning rejects in acidic than
neutral conditions, unlike many other metals (Jones & Ruppert, 2017). Mo has
been shown to become more mobile in procedures that use deionized water as a
leachant, which may be similar to actual disposal conditions unlike many other
coal ash elements that are more mobile when subjected to weak acid (Jones &
Ruppert, 2017).
pH
Detected Range: 4.2 -11.1 S.U. in 94 samples
Concentrations in 39 samples exceeded the PBTV. Concentrations in 65
samples exceeded the 2L.
pH exceeds the PBTV and 2L in pore water, transition zone and bedrock
groundwater beneath the ash basin.
pH downgradient of the ash basin exceeds the PBTV and 2L were
observed in shallow, transition zone, and bedrock groundwater.
The pH scale is used to measure acidity or alkalinity. A pH value of 7 indicates
neutral water. A value lower than the USEPA-established SMCL range (<6.5
Standard Units) is associated with a bitter, metallic tasting water, and corrosion.
A value higher than the SMCL range (>8.5 Standard Units) is associated with a
slippery feel, soda taste, and deposits in the water (USEPA, 2013c).
In a statistical summary of groundwater quality in North Carolina, the
Superfund Research Program at UNC analyzed 618 private well water samples
for pH in Cleveland and Rutherford Counties. The samples were analyzed by the
North Carolina State Laboratory of Public Health from 1998 – 2012. This study
found that 16.9% of wells in Cleveland County and 20.3% of wells in Rutherford
County had a pH result outside of the USEPA’s SMCL range (Table 11-1).
Using the USGS NURE database, all pH tests within a 20-mile radius of CSS are
shown on Figure 11-65; with a pH range from 5.1 to 8.7.
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Selenium
Reported Range: 0.122 µg/L – 300 µg/L; Number of Detections/Total Samples:
31/94
Concentrations in 23 samples exceeded the PBTV.
Selenium exceeds the PBTV in pore water and transition zone beneath the
ash basin.
Selenium reported in groundwater downgradient of the ash basin
including exceedances of PBTV in shallow and transition zone
groundwater.
Selenium concentrations from 31 soil samples beneath the ash basin and
downgradient of the ash basin exceed the PSRG for POG value but only 9
samples exceed the PBTV.
Selenium is a semi-metallic gray metal that commonly occurs naturally
combined with rocks and soil. It is common to find trace amounts of selenium in
food, drinking water, and air-borne dust. Over geologic time, selenium has been
introduced to the earth’s surface and atmosphere through volcanic emissions
and igneous extrusions. Weathering and transport partition the element into
residual soils, where it is available for plant uptake, or to the aqueous
environment, where it may remain dissolved, enter the aquatic food chain, or
redeposit within a sedimentary rock such as shale (Institute, 2008a).
Groundwater containing selenium is typically the result of either natural
processes or industrial operations. Naturally, selenium’s presence in
groundwater is from leaching out of selenium-bearing rocks. It is most common
in shale ranging from 0.6 to 103 mg/kg. Anthropogenically, selenium is released
as a function of the discharge from petroleum and metal refineries and from ore
mining and processing facilities. Ore mining may enhance the natural erosive
process by loosening soil, creating concentrations in erodible tailings piles, and
exposing selenium containing rock to runoff (Martens, 2002); USEPA 2014).
In a statistical summary of groundwater quality in North Carolina, the
Superfund Research Program at UNC analyzed 399 private well water samples
in Stokes and Rockingham counties from 1998-2010. The values ranged from 2.5
to 26 µg/L, and no samples exceeded the 50 µg/L primary MCL for selenium
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(NCDHHS, 2010). The mean concentration in both counties was 2.7 µg/L. The
selenium summary statistics from this study are reported in Table 11-1.
Strontium
Reported Range: 3.3 µg/L – 4,450 µg/L; Number of Detections/Total Samples:
83/94
Concentrations in 41 samples exceeded the PBTV.
Strontium exceeds the PBTV in pore water, transition zone, and bedrock
groundwater beneath the ash basin.
Strontium detected in groundwater downgradient of the ash basin
including exceedances of PBTV in shallow, transition zone, and bedrock
groundwater.
Historic detections generally show decreasing or stable concentrations
overtime for each flow layer except at locations northwest of the ash basin.
Strontium is a soft silver-yellow alkaline earth metal. It is highly chemically
reactive and forms a dark oxide layer when it interacts with air. It is chemically
similar to Ca and replaces Ca or K in igneous rocks in minor amounts. Strontium
is generally present in low concentrations in surface waters but may exist in
higher concentrations in some groundwater (Hem, 1985).
Sr is present as a minor coal and coal ash constituent. Sr has been observed to
leach from coal cleaning rejects more in neutral conditions than acidic, unlike
many other metals (Jones & Ruppert, 2017). It has been shown to behave
conservatively in surface waters downstream of coal plants (Ruhl, et al., 2012).
Sulfate
Reported Range: 0.0454 µg/L – 1,540 µg/L; Number of Detections/Total Samples:
82/94
Concentrations in 36 samples exceeded the PBTV. Concentrations in 6
samples exceed 2L.
Sulfate exceeds the PBTV and 2L in pore water beneath the ash basin; and
transition zone groundwater downgradient of the basin.
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Sulfate detected in groundwater downgradient of the ash basin including
exceedances of PBTV in shallow, transition zone, and bedrock
groundwater.
Historical exceedances generally show decreasing concentrations both
beneath the ash basin and downgradient of the ash basin except west of
the structural fill where concentrations are increasing overtime.
Sulfate is a naturally occurring substance found in minerals, soil, and rocks. It is
present in ambient air, groundwater, plants, and food. Primary natural sources
of sulfate include atmospheric deposition, sulfate mineral dissolution, and
sulfide mineral oxidation. The principal commercial use of sulfate is in the
chemical industry. Sulfate is discharged into water in industrial wastes and
through atmospheric deposition (2003). Anthropogenic sources include coal
mines, power plants, phosphate refineries, and metallurgical refineries.
While sulfate has an SMCL, and no enforceable maximum concentration set by
the USEPA, ingestion of water with high concentrations of sulfate may be
associated with diarrhea, particularly in susceptible populations, such as infants
and transients (USEPA, 2012). However, adults generally become accustomed to
high sulfate concentrations after a few days. It is estimated that about 3% of the
public drinking water systems in the United States may have sulfate
concentrations of 250 mg/L or greater (Miao, Brusseau, Carroll, & others, 2012).
Sulfate is on the list of enforced regulated contaminates that may cause cosmetic
effects or aesthetic effects in drinking water (USEPA, 2012).
In the Piedmont and Blue Ridge Aquifers chapter of the USGS Ground Water Atlas of
the United States, the groundwater of this region as a whole is described as
“generally suitable for drinking…but iron, manganese, and sulfate locally occur
in objectionable concentrations,” (U.S. Geological Survey, 1997).
Thallium
Reported Range: 0.016 µg/L – 8.39 µg/L; Number of Detections/Total Samples:
42/94
Concentrations in 22 samples exceeded the PBTV.
Thallium exceeds the PBTV in pore water and transition zone beneath the
ash basin.
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Thallium reported in groundwater downgradient of the ash basin
including exceedances of PBTV in shallow and transition zone
groundwater.
Pure thallium is a soft, bluish white metal that is widely distributed in trace
amounts in the earth's crust. In its pure form, it is odorless and tasteless. It can be
found in pure form or mixed with other metals in the form of alloys. It can also
be found combined with other substances such as bromine, chlorine, fluorine,
and iodine to form salts (Institute, 2008c).
Traces of thallium naturally exist in rock and soil. As rock and soil is eroded,
small amounts of thallium end up in groundwater. In a USGS study of trace
metals in soils, the variation in thallium concentrations in A (i.e., surface) and C
(i.e., substratum) soil horizons was estimated across the United States. The
overall thallium concentrations range from <0.1 mg/kg to 8.8 mg/kg. North
Carolina concentrations from this study are depicted in Figure 11-66. Thallium is
compared to an IMAC since no 2L Standard has been established for this
constituent.
In a study by the Georgia Environmental Protection Division (EPD) of the Blue
Ridge Mountain and Piedmont aquifers, 120 sites were sampled for various
constituents. Thallium was not detected at any of these sites (Method Reporting
Limit (MRL)=1 µg/L) (Donahue & Kibler, 2007).
TDS
Reported Range: 21 µg/L – 2,600 µg/L; Number of Detections/Total Samples:
90/94
Concentrations in 43 samples exceeded the PBTV. Concentrations in 18
samples exceeded the 2L.
TDS exceeds the PBTV in pore water, transition zone, and bedrock
groundwater beneath the ash basin. 2L exceedances occur in the pore
water, transition zone and bedrock groundwater.
TDS detected in groundwater downgradient of the ash basin including
exceedances of PBTV and 2L in shallow, transition zone and bedrock
groundwater.
Groundwater contains a wide variety of dissolved inorganic constituents as a
result of chemical and biochemical interactions between the groundwater and
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the elements in the soil and rock through which it passes. Total Dissolved Solids
(TDS) mainly consist of cation and anion particles (e.g., calcium, chlorides,
nitrate, phosphorus, iron, sulfur, and others) that can pass through a 2 micron
filter (USEPA, 1997). TDS is therefore a measure of the total amount of dissolved
ions in the water, but does not identify specific constituents or explain the nature
of ion relationships. TDS concentrations in groundwater can vary over many
orders of magnitude and generally range from 0 – 1,000,000 µg/L. The ions listed
below are referred to as the major ions as they make up more than 90 percent of
the TDS in groundwater. TDS concentrations resulting from these constituents
are commonly greater than 5,000 µg/L (Freeze & Cherry, 1979).
Sodium (Na+)
Magnesium (Mg2+)
Calcium (Ca2+)
Chloride (Cl-)
Bicarbonate (HCO3-)
Sulfate (SO42-)
Minor ions in groundwater include: boron, nitrate, carbonate, potassium,
fluoride, strontium, and iron. TDS concentrations resulting from minor ions
typically range between 10 – 1,000 µg/L (Freeze & Cherry, 1979). Trace
constituents make up an even smaller portion of TDS in groundwater and
include: aluminum, antimony, arsenic, barium, beryllium, cadmium, chromium,
cobalt, lead, manganese, nickel, selenium, thallium, vanadium, and zinc among
others. TDS concentrations resulting from trace constituents are typically less
than 100 µg/L (Freeze & Cherry, 1979). In some cases, contributions from
anthropogenic sources can cause some of the elements listed as minor or trace
constituents to occur as contaminants at concentration levels that are orders of
magnitude above the normal ranges indicated above.
TDS in water supplies originate from natural sources, sewage, urban and
agricultural run-off, and industrial wastewater. Salts used for road de-icing can
also contribute to the TDS loading of water supplies. Concentrations of TDS from
natural sources have been found to vary from less than 30 mg/L to as much as
6,000 mg/L. Water containing more than 2,000 – 3,000 mg/L TDS is generally too
salty to drink (the TDS of seawater is approximately 35,000 mg/L) (Freeze &
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Cherry, 1979). Reliable data on possible health effects associated with the
ingestion of TDS in drinking water are not available. (WHO, 1996) TDS is on the
list of “National Secondary Drinking Water Regulations” (NSDWRs) which are
non-enforced regulated contaminates that may cause cosmetic effects or aesthetic
effects in drinking water (USEPA, 2013c)
In the April 2015 CCR Rule, the USEPA listed TDS as an indicator constituent
(along with boron, calcium, chloride, fluoride, pH, and sulfate). USEPA defines
indicator constituents as those that are present in CCR and would rapidly move
through the surface layer, relative to other constituents, and thus provide an
early detection of whether contaminants are migrating from the CCR unit
(USEPA CCR Rule, 2015).
Vanadium
Reported Range: 0.093 µg/L – 948 µg/L; Number of Detections/Total Samples:
84/94
Concentrations in 17 samples exceeded the PBTV. Concentrations in 64
samples exceeded the IMAC.
Vanadium exceeds the PBTV and IMAC in pore water, transition zone,
and bedrock groundwater beneath the ash basin.
Vanadium exceeds the PBTV and IMAC in shallow, transition zone, and
bedrock groundwater downgradient the ash basin.
Historic detections generally show stable or decreasing concentrations
overtime for each flow layer beneath the ash basin and downgradient the
ash basin.
Vanadium concentrations from 108 soil samples beneath the ash basin and
downgradient of the ash basin exceed the PSRG for POG value but only 9
samples exceed the PBTV.
Vanadium is widely distributed in the earth’s crust at an average concentration
of 100 ppm (approximately 100 mg/kg), similar to that of zinc and nickel.
Vanadium is the 22nd most abundant element in the earth’s crust (Institute,
2008d). V(V) and V(IV) are the most important species in natural water, with
V(V) likely the most abundant under environmental conditions (Wright & Belitz,
2010). Vanadium is compared to IMAC since no 2L standard has been
established for this constituent by NCDEQ. Vanadium is estimated to be the
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22nd most abundant element in the crust (0.011 weight percent, (Parker, 1967).
Vanadium occurs in four oxidation states (V5+, V4+, V3+, and V2+). It is a common
trace element in both clay minerals and plant material. The National Uranium
Resource Evaluation (NURE) program was initiated by the Atomic Energy
Commission in 1973 with a primary goal of identifying uranium resources in the
United States (Smith, 2006). The Hydrogeochemical and Stream Sediment
Reconnaissance (HSSR) program (initiated in 1975) was one component of
NURE. Planned systematic sampling of the entire United States began in 1976
under the responsibility of four Department of Energy (DOE) national
laboratories. Samples were collected from 5,178 wells across North Carolina. Of
these, the concentration of vanadium was equal to or higher than the IMAC in
1,388 well samples (27 percent).
Pending Investigations 11.3
Additional metal oxy-hydroxide phases of iron (HFO) and aluminum (HAO) data are
needed to support geochemical modeling conducted as part of the CAP. Soil and rock
samples from previously installed borings or from additionally drilled boreholes along
the primary groundwater flow transect will be used. The samples will be located:
Directly beneath the ash basin
Downgradient locations north of the ash basin
Downgradient locations northwest of the ash basin
The samples will be collected at vertical intervals that coincide with nearby well screen
elevations. Analysis results of collected samples will be used to improve input
parameters for the updated geochemical model.
To help determine potential routes of exposure and receptors related to the ash basin,
additional surface water samples will be collected from Belews Reservoir and the Dan
River near the stream/river bank most likely to be impacted by potentially
contaminated groundwater discharge. Surface water samples to be collected in Belews
Reservoir will include three upgradient sample locations and one downgradient sample
location. Additionally, three samples will be collected from locations at the point of
convergence with Belews Reservoir and AOW streams (S-6, S-7, S-13 and S-14) and the
stream downgradient of wells GWA-4S/D. Surface water samples from the Dan River
will include three background locations; two in the Dan River and one in the tributary
stream, Town Fork Creek. Four additional samples will be collected downgradient of
background locations. Locations will be sampled at a frequency and at the same
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physical location to allow an assessment with 15A NCAC 02B water quality standards.
At each location, two samples will be collected within one hour to be evaluated for
acute instream metals standards and the remaining two samples will be collected
within the following 95 hours to be evaluated, using an average of a minimum of four
samples, for chronic instream metals standards.
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12.0 RISK ASSESSMENT
A baseline human health and ecological risk assessment was performed in 2016 as a
component of CAP Part 2 for the Belews Creek Steam Station (HDR, 2016d). The risk
assessment characterized potential effects on humans and wildlife exposed to coal ash
constituents present in environmental media for the purpose of aiding corrective active
decisions. Implementation of corrective action is intended to achieve future site
conditions protective of human health and the environment, as required by CAMA.
This update to the risk assessment evaluates groundwater and surface water results
collected since the 2016 risk assessment (November 2015 to June 2017) in order to
confirm or update risk conclusions in support of remedial actions. Data used in the
2016 risk assessment included groundwater, surface water, sediment, AOW water and
soil collected from January 2011 through October 2015 (HDR, 2016). This update to the
risk assessment uses sampling locations described in Section 3.2 of the 2016 document,
unless otherwise noted. As previously noted, AOW locations are outside the scope of
this risk assessment because AOWs, wastewater, and wastewater conveyances (effluent
channels) are permitted under the NPDES Program administered by NCDEQ DWR.
This process is on-going in a parallel effort to the CSA and subject to change.. No new
sediment or soil samples, with exception of background soils, have been collected that
are applicable to the 2016 risk assessment, therefore risk estimates associated with those
media have not been re-evaluated.
As part of the 2016 risk assessment, human health and ecological conceptual site models
(CSMs) were developed to guide identification of exposure pathways, exposure routes,
and potential receptors for evaluation in the risk assessment. The CSMs (CAP Part 2,
Appendix F, Figures 2-3 and 2-4) describe the sources and potential migration pathways
through which groundwater beneath the ash basin may have transported coal ash
constituents to other environmental media (receiving media) and, in turn, to potential
human and ecological receptors. Exposure scenarios and exposure areas were
presented in detail in Sections 2 and 5 of the 2016 risk assessment (CAP Part 2,
Appendix F).
This risk assessment update included the following:
Identification of maximum constituent concentrations for groundwater and
surface water
Inclusion of new groundwater and surface water data to derive overall average
constituent concentrations for exposure areas
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Comparison of new maximum constituent concentrations to the 2016 risk
assessment human health and ecological screening values
Comparison of new maximum constituent concentrations to site-specific 2016
human health Risk-Based Concentrations (RBC)
Incorporation of new maximum constituent concentrations into wildlife Average
Daily Dose (ADD) calculations for comparison to ecological Toxicity Reference
Values (TRVs)
Evaluation of new groundwater and surface water data collected since the 2016 risk
assessment and their influence on potential risks are summarized below by exposure
area (Figure 12-1).
Human Health Screening Summary 12.1
On-Site Groundwater
Groundwater sample locations included in the assessment were: MW-102S through
MW-204D, GWA-1S through GWA-17D and AB-1S through AB-9D, excluding ash pore
water wells. These wells were evaluated because they represent the potential
trespasser/worker exposure area as determined in the 2016 risk assessment.
Groundwater analytical results are included in Appendix B, Table 1.
New maximum concentrations of antimony, arsenic, beryllium, hexavalent chromium,
nickel, and selenium were detected that exceeded human health risk screening values;
however, no values exceeded respective site-specific RBCs. There is no evidence these
constituents pose human health risks from groundwater exposure.
On-Site Surface Water
Surface water sample locations included in the 2016 risk assessment were: SW-BL-D,
SW-DR-D and SW-DR-U (Figure 12-1). The sample location SW-DR-D is adjacent to
NPDES outfall 003 discharging ash sluice and FGD wastewater and is not
representative of Dan River conditions downstream of plant operations. Thus, SW-DR-
D is influenced by the NPDES outfall and not a subject of CAMA. Results for the
surface water sample locations are included in Appendix B, Table 2.
New maximum concentrations of boron, cobalt, manganese, molybdenum, and
thallium exceeded on-site surface water risk screening values. Concentrations of boron,
manganese and molybdenum did not exceed respective RBCs; therefore, no risks to
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humans (trespasser/worker) exposed to these constituents in on-site surface water were
identified.
New maximum concentrations for cobalt (7.8 µg/L) and thallium (1.1 µg/L) were
detected at SW-DR-U on the Dan River. The 2016 risk assessment identified potential
risk under a hypothetical recreational and subsistence fisher scenario exposed to
thallium in fish tissue modeled from surface water concentrations. Similarly, the 2016
risk assessment identified potential risk under a hypothetical subsistence fisher scenario
exposed to cobalt in modeled fish tissue. The risks were likely overestimated because
of very conservative assumptions in the exposure models. Concentrations of cobalt and
thallium have decreased in subsequent sampling events and have not exceeded the
respective human health screening levels of 1 µg/L (cobalt) and 0.2 µg/L (thallium) in
the two most recent sampling events at SW-DR-U. Thus, there is no evidence of
potential risks under the hypothetical fisher scenario from exposure to cobalt and
thallium at SW-DR-U.
Ecological Screening Summary 12.2
Exposure Area 3 – Surface Water
One surface water sample location was included in the assessment for Ecological
Exposure Area 3: SW-BL-D in Belews Reservoir (Figure 12-1). Results for the surface
water sample location are included in Appendix B, Table 2. The 2016 risk assessment
resulted in no LOAEL-based HQ greater than unity in Exposure Area 3 surface water
for the ecological receptors evaluated.
A new maximum concentration of cobalt exceeded the surface water ecological risk
screening value. The concentration cobalt did not affect wildlife ADDs to the extent
that the TRV was exceeded (HQ<1). No evidence of risks to ecological receptors
exposed to cobalt in Exposure Area 3 surface water identified. In addition, Belews
Reservoir is considered beyond the extent of constituent migration in groundwater
from the ash basin.
Private Well Receptor Assessment Update 12.3
An independent study was conducted that evaluated 2015 groundwater data collected
from 24 private drinking water wells within close proximity of the Belews Creek Steam
Station (HDR 2016; Haley & Aldrich, 2015). Pertinent observations presented in the
study included:
Groundwater flow paths from BCSS CAMA areas are not in the direction of
private wells.
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The concentration of boron and other potential coal ash indicators were low and
not above screening levels in the private wells sampled by NCDEQ with three
exceptions. Cobalt, molybdenum and arsenic were above the state screening
levels, DHHS screening level and the 2L, respectively.
Hexavalent chromium and vanadium were detected in some wells above their
respective DHHS screening levels, but at concentrations consistent with regional
background.
Recent (2017) results from off-site private water supply wells sampled since the Haley &
Aldrich assessment (2015) were compared to 2L, as well as U.S. EPA’s Maximum
Contaminant Levels (MCL) and tap water Regional Screening Levels (RSL). Key
observations from evaluation of the private well groundwater data include:
Concentrations of boron were consistent with previous observations.
Arsenic exceeded the 2L of 10 µg/L in samples collected from six wells (BC17,
BC20, BC30, BC32, BC34, BC35). Due to their distance from the ash basin and
based on groundwater flow to the north, these wells are not considered to be
impacted by the ash basin.
Chromium exceeded the 2L of 10 µg/L in samples collected from one location
(BC33), although chromium concentrations were less than the MCL and tap
water RSL.
Cobalt exceeded the 2L of 1 µg/L at one location (BC23-5); however, the
concentration was less than the tap water RSL of 6 mg/L.
Iron exceeded the 2L of 300 µg/L in samples collected from 15 locations, but was
less than the tap water RSL of 14,000 µg/L.
Manganese exceeded the 2L of 50 µg/L in samples collected from seven locations,
but was less than the tap water RSL of 430 µg/L at all locations.
Vanadium exceeded 2L in samples collected from 22 locations, but was less than
the tap water RSL at all locations.
While several wells located to the west-southwest and northeast of the ash basin had
concentrations of chromium, cobalt, iron, manganese, vanadium that exceeded their
respective 2L, all detected concentrations were less than their respective tap water RSLs.
Based on the bedrock groundwater flow direction at the site (Figures 6-10 and 6-11,
discussed in Section 6.3) private water supply wells located west of the ash basin along
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Old Plantation Road (BC2019-RAW, BC2 Well 1, BC2 Well 2, BC-1007, BC4, BC4A and
BC4B) are located sidegradient to the ash basin. The remaining water supply wells
identified in the area are located upgradient or sidegradient substantially beyond the
expected flow zone of the BCSS ash basin.
The water supply wells do not show indications of being impacted by the ash basin.
The water chemistry signature of the water supply wells is similar to the background
bedrock wells at the site. Although several water supply wells exceeded the site
specific BTVs, concentrations in these water supply wells are within the background
concentration range for similar Piedmont geologic settings.
Risk Assessment Update Summary 12.4
Based on review and analysis of groundwater and surface water data, there is no
evidence of risks to humans and wildlife at BCSS attributed to CCR constituent
migration in groundwater from the ash basins. This update to the human health and
ecological risk assessment supports a proposed NCDEQ Risk Classification of “Low”.
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13.0 GROUNDWATER MODELING RESULTS
Groundwater flow and transport, and geochemical models are being developed to
simulate movement of constituents of interest (COI) through the subsurface to support
the evaluation and design of remedial options at the sites. The models will provide
insights into:
1) COI mobility: Geochemical processes affecting precipitation, adsorption and
desorption onto solids will be simulated based on lab data and
thermodynamic principles to predict partitioning and mobility in
groundwater.
2) COI movement: Simulations of the groundwater flow system will be
combined with estimates of source concentrations, sorption, effective
porosity, and dispersion to predict the paths and rates of constituent
movement at the field scale.
3) Scenario Screening: The flow, transport and geochemical models will be
adjusted to simulate how various ash basin closure design options and
groundwater remedial technologies will affect the short-term and long-term
distribution of COIs.
4) Design: Model predictions will be used to help design basin closure and
groundwater corrective action strategies in order to achieve compliance with
2L in a reasonable cost and timeframe.
The groundwater flow model linked with the transport model will be used to establish
transport predictions that best represent observed conditions at the site particularly for
the constituents, such as boron, that are negligibly affected by geochemical processes.
The geochemical model information will provide insight into the complex processes
that influence constituent mobility, which will be used to refine constituent sorption
within the transport model. Once the flow, transport and geochemical models for the
site accurately reproduce observed site conditions, they can be used as predictive tools
to evaluate the conditions that will result from various remedial options for basin
closure (No Change, Cap-in-Place or Ash Removal) and potential subsequent passive or
active groundwater remedial technologies.
The site-specific groundwater flow and transport models and the site-specific
geochemical models are currently being updated for use in the CAP. The CAP will
further discuss the purpose and scope of both the groundwater and geochemical
models. It will detail model development, calibration, assumptions and limitations.
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The CAP will also include a detailed remedial option evaluation, based on observed
conditions and the results of predictive modeling. The evaluation of the potential
remedial options will include comparisons of predictive model results for long-term
source concentration and plume migration trends toward potential receptors. The
model predictions will be used in combination with other evaluation criteria to develop
the optimal approach for basin closure and groundwater remediation.
The following sections provide a brief summary of modeling efforts completed to date
at BCCS.
Summary of Fate and Transport Model Results 13.1
The initial groundwater flow and transport model was developed by HDR in
conjunction with University of North Carolina at Charlotte (UNCC) to gain an
understanding of COI migration after closure of the ash basin at the BCCS. The initial
groundwater model presented in the CAP Part 1 (HDR, 2015b) included a calibrated
steady-state flow model of July 2015 conditions; a calibrated historical transient model
of constituent transport to match June/July 2015 conditions; and three potential basin
closure scenarios. Those basin closure simulation scenarios included:
No change in site conditions (basin remains open, as is)
Cap-in-place
Ash removal (excavation)
The initial model used arsenic, beryllium, boron, chloride, chromium, chromium VI,
cobalt, and thallium as primary modeling constituents. In addition, the remedial
alternative evaluation simulations were run to a total time of 250 years.
The revised model in the CAP Part 2 (HDR, 2016d) included a calibrated steady-state
flow model of June 2015 conditions; a calibrated historical transient model of
constituent transport to June/July 2015 conditions; and two potential basin closure
scenarios. Those basin closure simulation scenarios included:
No change in site conditions (basin remains open, as is)
Cap-in-place
As a portion of interim remedial action at the site the flow and transport model was
revised. The revised model was focused on evaluating hydraulic impacts to the
northwest corner of the ash basin for the interim remedial action. The results of the
model were presented as Appendix C of the Basis of Design Report for the Interim
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Action Plan (SynTerra, 2017a). The model was revised by HDR which included:
expanding the grid; modifications to the layering; refinements to hydraulic
conductivity; modification of the sorption coefficient (Kd) based on geochemical
modeling; adjustment of source pore water concentrations; and incorporation of
proposed provisional background concentrations (PPBC). SynTerra used the updated
HDR model and simulated four extraction wells to evaluate the hydraulic impacts to
the northwest corner of the ash basin.
The flow and transport model is currently being modified as a part of the updated CAP
and will include: development of a calibrated steady-state flow model that includes
data available through November 2017; development of a historical transient model of
constituent transport; and predictive simulations of basin closure plus groundwater
corrective action scenarios. The updated fate and transport model will consider boron,
and additional COIs that are hydraulically driven. Predictive simulations will have
simulation times that continue until modeled COI concentrations are below the 2L
standard/IMAC at the compliance boundary.
The following sections provide a brief summary of the groundwater modeling that was
presented in the CAP Part 2, and a general outline for the updated modeling effort. The
summary of the groundwater modeling presented in the CAP Part 2 was compiled to
address specific questions regarding model set-up and calibration. A complete updated
groundwater flow and transport model report is being developed and will be submitted
as part of the updated CAP.
The model was developed using the MODFLOW-NWT version (Niswonger, Panday, &
Motomu, 2011). This version provides improved numerical stability and accuracy for
modeling problems within a variable water table. The improved numerical stability
and accuracy can provide better estimates of the water table fluctuations that result
from ash basin operating conditions and potential closure and groundwater corrective
action activities.
MT3DMS was used to simulate fate and transport of selected COIs. MT3DMS uses the
groundwater flow field from MODFLOW to simulate 3D advection and dispersion of
the dissolved COIs, including the effects of retardation due to the soil matrix adsorption
of COIs.
Flow Model Construction 13.1.1
The flow and transport model was built through a series of steps. The first step
was to build a three-dimensional (3D) model of the Site hydrostratigraphy based
on the SCM. The next steps were to determine the model dimensions and the
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construction of the numerical grid. The numerical grid was then populated with
flow parameters, which were calibrated in the steady-state flow model. Once the
flow model was calibrated, the flow parameters were used to develop a transient
model of the historical flow patterns at the site. The historical flow model was
then used to provide the time-dependent flow field for the constituent transport
simulations.
Hydraulic parameters such as hydraulic conductivity values may be adjusted
within reasonable site-specific conditions to achieve hydraulic head calibration
error below 10%.
Flow Model Domain and Grid Layers
The HDR model has dimensions of approximately 11,000 feet north to south,
10,000 feet east to west, with the ash basin at the center of the model domain.
The model domain was not rotated, but is parallel to the Dan River.
The hydrostratigraphic model consists of five units: ash/dam/fill material,
soil/saprolite, saprolite, transition zone and fractured bedrock. Those units were
determined by interpolating boring log data from historical data, the CSA, and
the CAP reports (HDR, 2015a), (2015b), (2016).
The numerical grid consists of rectangular blocks arranged in columns, rows,
and layers. The model was developed using a 40-foot by 40-foot grid. The grid
consists of 11 layers representing the five hydrostratigraphic units. It is expected
grid layers and spacing will be adjusted for in the updated model.
Flow Model Boundary Conditions
The northwest model boundary which represents the Dan River was set to a
specified head within the fractured bedrock. Drain features such as the small
catchments to the west of the site and the unnamed stream downgradient of the
ash basin dam were applied as hydraulic boundaries. The ash basin pond and
Hydrostratigraphic layer Grid layer
Ash/Dam/Fill 1-4
M1 Soil/Saprolite 5-6
M2 Saprolite 7
Transition Zone 8-9
Fractured Bedrock 10-11
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other small water bodies within the model domain were also set as constant head
boundaries.
Sources and Sinks
Water can enter the model or leave the model through the use of sources and
sinks. MODFLOW uses point sources/sinks as well as aerial sources/sinks. Point
sources/sinks include rivers, wells, drains, and general head. Aerial
sources/sinks considered are limited to recharge.
Source (Recharge)
Model recharge sources in the current model include:
Recharge outside of the ash basin ranges from 3 to 9 inches per
year.
Rainwater that infiltrates
Constant head boundaries
Model Sinks (Drains)
Model sinks in the current model include:
Streams within the model domain
Constant head boundaries
AOWs (14 with measurable flow)
Water Supply Wells
A total of 6 domestic supply wells have been identified within the model domain
of the CAP Part 2 model (HDR, 2016). The average daily use for domestic wells
was set at a discharge of approximately 400 gallons per day (USEPA, 2015). The
model domain will be expanded to include additional domestic and public
supply wells.
Hydraulic Conductivity
The horizontal hydraulic conductivity and the horizontal-to-vertical hydraulic
conductivity anisotropy ratio (anisotropy) are the main variable hydraulic
parameters in the model. The distribution of those parameters is based primarily
on the model hydrostratigraphy, with some local variations. The values can be
adjusted during the calibration process to provide a best fit for observing water
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levels in wells. Initial estimates of parameters were based on literature values,
results of slug and core testing, and simulations performed using a preliminary
flow model.
Streams and Lake Hydraulic Parameters
The ash basin was represented as a specific head boundary. The stage of the ash
pond was set at 750 feet.
Flow Model Calibration Targets
The steady state flow model calibration data for June 2015 were presented in the
CAP Part 2. In the final CAP, calibration target data will be incorporated by
taking the mean of the hydraulic head data for each well and applying a
standard deviation to reflect the seasonal changes in the hydraulic heads.
Hydraulic head data will include measurements through November 2017.
Mass Balance
The previous model had a mass balance error of well below 1%. The updated
model will have a similar numerical accuracy.
Flow Model Sensitivity Analysis
A flow model sensitivity analysis was conducted by varying the recharge rates
and hydraulic conductivities in the shallow and transition zones. The change to
the Normalized Root Mean Square of the Error was observed. The model was
most sensitive to varying horizontal hydraulic conductivity within the shallow
zone, followed by recharge outside the basin, then recharge to the ash basin. The
model was least sensitive to varying vertical hydraulic conductivity of the
shallow zone and transition zone. Since no major elements within the model are
to be changed, there is no need to perform additional sensitivity testing.
Particle Tracking
A primary concern is the potential impact to domestic and public wells from
COIs emanating from the Site. The final calibrated groundwater flow model will
be used to assess potential impacts by considering pumping from domestic and
public wells within the model domain.
Flow Model Assumptions and Limitations
The groundwater model is currently being refined therefore the assumptions and
limitations are subject to change. Based on the preliminary modeling results, the
assumptions and limitations include the following:
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The steady-state flow model was calibrated to hydraulic heads
measured in monitoring wells in July 2015. The model was not
calibrated to transient water levels over time, recharge, or river flow.
MODFLOW simulates flow through porous media. A single domain
MODFLOW modeling approach for simulating flow in the primary
porous groundwater zones and bedrock was used for contaminant
transport. Flow in fractured bedrock is simulated using the equivalent
porous media approximation.
For the purposes of numerical modeling and comparing predictive
scenarios, it was previously assumed that basin closure would be
completed in 2015. A similar assumption will be used in the updated
model.
Predictive simulations were performed and steady-state flow conditions
were assumed from the time that the ash basin was placed in service
through the current time until the end of the predictive simulations
(2115).
The uncertainty in model parameters and predictions has not been
quantified; therefore, the error in model predictions is not known. It was
assumed the model results are suitable for a relative comparison of
closure scenario options.
In the fate and transport model found in the Appendix C of the Basis of
Design Report for the Interim Action Plan (SynTerra, 2017a) Belews Lake
and the Dan River were modeled as constant head boundaries in the
numerical model. It was not possible to assess the effects of pumping
wells or other groundwater sinks that are near the Dan River. However,
this boundary condition can be modified to allow for groundwater
remediation simulations. Residential wells were assumed to be
completed in one of three bedrock model layers.
Transport Model Construction 13.1.2
Modular 3-D Transport Multi-Species (MT3DMS) is being used to simulate
constituent transport. MT3DMS simulates 3D advection and dispersion of the
dissolved COIs, including the effects of retardation due to the soil matrix
adsorption of COIs based on flow fields established by MODFLOW. The initial
model used arsenic, beryllium, boron, chloride, chromium, chromium VI, cobalt,
and thallium as primary modeling constituents. The updated fate and transport
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modeling will focus on boron and additional COIs that are hydraulically driven.
Other constituents will be considered using the geochemical model.
Transport Model Parameters
The key transport model parameters (besides the flow field) are the constituent
source concentrations in the ash basin and the constituent soil-water distribution
coefficients (Kd). Secondary parameters are the longitudinal, transverse, and
vertical dispersivity, and the effective porosity.
Transport Model Boundary Conditions
In the current model, the transport model boundary conditions are “no flow” on
the exterior edges of the model. Infiltrating rainwater is assumed to be clean and
enters with zero concentration from the top of the model. Contaminants are
assumed to leave the model when they reach a drain or are removed by flow that
enters a constant head boundary.
In the current model, the concentrations from the June 2015 sampling event were
set as boundary conditions within the ash basin. These values will be updated to
use the concentration data up through the fourth quarter 2017 sampling event.
Transport Model Sources and Sinks
Transport model sources include:
The ash basin is the source of COIs in the model. The sources are
simulated by applying a constant COI concentration within the cells of
the ash basin and were applied to layers 1 through 4 which represent the
ash. This allows infiltrating water to carry dissolved constituents from
the ash pore water into the groundwater underneath the ash basin.
As the COIs migrate beneath and away from the coal ash, zones of soil
and fractured rock become impacted. These impacted zones can serve
as secondary sources, and are fully accounted for in the transport
models. For simulations that involve ash excavation, the constant
concentration sources in the ash zones are removed, but the secondary
sources in the impacted soil and fractured bedrock remain. The
longevity of these secondary sources depends on the COI Kd, and on the
degree of flushing by infiltration and groundwater flow.
Transport model sinks include:
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Streams
Drain Boundaries
Transport Model Calibration Targets and Sensitivity
The initial transport model calibration targets were COI concentrations measured
in monitoring wells in June/July 2015. The updated model calibration targets
will include COIs concentrations measured in monitoring wells in 2017.
Constituents considered for the next fate and transport model will include boron
and other COIs. COIs not amenable to simulation in the fate and transport
model will be addressed in the geochemical model.
Transport Simulation
The updated model will be calibrated to include data through fourth quarter
2017 and will extend until modeled COI concentrations are below the 2L
standard at the compliance boundary. The following is a summary of the basin
closure options to be modeled:
No Action – Leave the ash basin as is to evaluate whether groundwater
quality would be restored by natural attenuation under current
conditions.
Cap-in-Place – Grade the ash and place an engineered low permeability
cover system to reduce infiltration of surface water. This scenario
assumes that the ash under the cap will be dewatered.
Ash Removal – Remove the ash from the basin. This scenario assumes
that the ground surface would be restored to its initial grade (prior to
construction of the ash basin).
The installation of a groundwater extraction system (or other
contemplated groundwater corrective system(s)).
The distribution of recharge, locations of drains, and distribution of material will
be modified to represent possible basin closure options. The results of these
simulations will be included as part of the updated CAP submittal.
Summary of Flow and Transport Modeling Results To 13.1.3
Date
The update model (presented in Appendix C of the Basis of Design Report for
the Interim Action Plan (SynTerra, 2017a)) predicts that ten extraction wells
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within the transition zone (model layer 6) will lower groundwater levels more
than 5 to 10 feet along the extraction system axis.
Modeling of boron shows little effect after pumping for six months. Pumping
simulations for longer period (five year) demonstrates a slight reduction of boron
concentrations along the extraction system axis.
The simulated June/July 2015 concentration distributions described in the CAP 1
(UNCC) (HDR, 2016d) were used as initial conditions in a predictive simulation
of future flow and transport at the Site and modeled arsenic, beryllium, boron,
chloride, chromium, cobalt, hexavalent chromium, and thallium. Predictive
simulations of future flow and transport for (CAP 2 (UNCC) (HDR, 2016d) used
the same COIs from CAP Part 1 modeling simulations. The “no action”, Cap-in-
place, and ash removal scenarios were run for a 250-year projection.
Site wide simulation data for the modified model will be presented in the
updated CAP.
No action
The CAP 1 (UNCC) (HDR, 2015b) groundwater simulations indicated arsenic at
the compliance boundary north of the dam will exceed the 2L standard.
Simulated beryllium, cobalt and thallium are predicted to exceed IMAC at the
compliance boundary within all three aquifer zones west of the dam and in
bedrock north of the dam by 2115. Boron simulations are above the 2L standard
at the compliance boundary north of the dam within the shallow, deep, and
bedrock zones by 2115. Chromium is predicted to exceed the 2L standard at the
compliance boundary north and west of the dam within the shallow, deep, and
bedrock zones. The hexavalent chromium simulation shows well AB-2S is above
the DHHS HSL standard, however is not above the DHHS HSL at the
compliance boundary within all three groundwater zones.
The CAP 2 (UNCC) (HDR, 2016) modeling scenario consists of modeling each
COI using the calibrated model for steady-state flow and transient transport
under the Existing Conditions scenario across the site to estimate when steady
state concentrations are reached at the Compliance Boundary. The model
indicates that arsenic, chloride, and chromium remain less than the 2L Standard
north and west of the dam in shallow, deep, and bedrock zones by 2115. In 2115,
boron is predicted to exceed the 2L Standard at the compliance boundary north
of the dam, but not west of the dam. Simulated beryllium will continue to be
below the IMAC at the compliance boundary after 100 years in all groundwater
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zones. Simulated cobalt is predicted to exceed IMAC at the compliance
boundary within all three aquifer zones north of the dam, but not west of the
dam by 2115. Simulated thallium is predicted to exceed IMAC at the compliance
boundary within all three aquifer zones due to a higher input concentration.
After 100 years, hexavalent chromium is predicted to be greater than the
NCDHHS HSL at the compliance boundary in all groundwater zones due to
higher background concentration inputs.
Cap-in-place
The Cap-in-place scenario presented in the CAP 1 (UNCC) (HDR, 2015b)
simulates the effects of placing an engineered cap over the ash basin. The model
assumes the pond is drained and covered and has an applied recharge of zero.
Simulations indicated arsenic north of the dam will exceed the 2L standard
within the transition zone and bedrock at the compliance boundary, but
decreases in the shallow aquifer. Simulated beryllium is below the 2L standard
at the compliance boundary within the shallow, deep, and bedrock zones prior to
2115. Simulated boron north of the dam exceeds the 2L standard initially then
dramatically declines and remains below standard within the shallow, deep, and
bedrock zones around 5 to 35 years after 2015. Chromium has the same
prediction as the No action scenario where the concentrations exceed the 2L
standard at the compliance boundary to the north and west of the dam within
the shallow, deep, and bedrock zones. The hexavalent chromium simulation is
similar to the No Action and Excavation scenarios. The simulation shows well
AB-2S is above the DHHS HSL standard for hexavalent chromium, however is
not above the DHHS HSL at the compliance boundary within all three
groundwater zones. Simulated cobalt and thallium are predicted to exceed
IMAC at the compliance boundary within all three aquifer zones west of the dam
and in bedrock north of the dam by 2115.
The CAP 2 (UNCC) (HDR, 2016d) modeling scenario consists of modeling each
COI using the calibrated model for steady-state flow and transient transport
under the Cap-in-place scenario at the site to estimate when steady state
concentrations are reached at the Compliance Boundary. The model indicates
that arsenic, chloride, and chromium remain less than the 2L Standard north and
west of the dam in shallow, deep, and bedrock zones by 2115. In 2115, boron is
predicted to exceed the 2L Standard in the shallow, deep and bedrock zones.
Simulated beryllium, will continue to be below the IMAC at the compliance
boundary after 100 years in all groundwater zones. Similar to the No action
simulation, cobalt and thallium are predicted to exceed IMAC at the compliance
boundary within all three aquifer zones north of the dam by 2115. After 100
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years, hexavalent chromium is predicted to be greater than the NCDHHS HSL at
the compliance boundary in all groundwater zones due to higher background
concentration inputs.
Excavation Scenario
The Excavation scenario presented in the CAP 1 (UNCC) (HDR, 2015b) simulates
the effects of removing the ash basins, the dikes, and ash storage areas at the
beginning of this scenario. Simulated arsenic concentrations decrease below the
2L standard at the compliance boundary within all three groundwater zones
prior to 2115. Simulated beryllium concentrations are similar to the Cap-in-place
results where it is below the 2L standard in the shallow, deep, and bedrock
zones. The simulated boron behavior is similar to the Cap-in-place scenario
where boron north of the dam exceeds the 2L standard initially then dramatically
declines and remains below standard within all three groundwater zones around
5 to 35 years after 2015. Unlike the No action and Cap-in-place scenarios,
simulated chromium concentrations decrease below the 2L standard at the
compliance boundary in the shallow, deep, and bedrock zones before 2115. The
hexavalent chromium simulation is similar to the No Action and Cap-in-place
scenarios. The simulation shows well AB-2S is above the DHHS HSL standard
for hexavalent chromium, however is not above the DHHS HSL at the
compliance boundary within all three groundwater zones. Simulated cobalt is
predicted to exceed IMAC at the compliance boundary north of the dam by 2115.
Thallium is predicted to decrease below the IMAC at the compliance boundary
within the shallow, deep, and bedrock zones.
Summary of Geochemical Model 13.2
The Belews Creek Site geochemical model investigates how variations in geochemical
parameters affect movement of constituents through the subsurface. The geochemical
site conceptual model (SCM) will be updated as additional data and information
associated with Site constituents, conditions, or processes are developed. The
geochemical modeling approach presented in the following sections was developed
using laboratory analytical procedures and computer simulations to understand the
geochemical conditions and controls on groundwater concentrations in order to predict
how remedial action and/or natural attenuation may occur at the site and avoid
unwanted side effects. The final geochemical model will be presented in the updated
CAP.
Model Construction 13.2.1
The geochemical model in the CAP Part 2 (HDR, 2016) included:
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Eh-pH (Pourbaix) diagrams showing potential stable chemical phases of
the aqueous electrochemical system, calibrated to encompass conditions at
the Site;
Sorption model where the aqueous speciation and surface complexation
are modeled using the USGS geochemical modeling program PHREEQC,
Simulations of the anticipated geochemical speciation that would occur
for each COI in the presence of adsorption to soils and in response to
changes in Eh and pH, and
Attenuation calculations where the potential capacity of aquifer solids to
sequester constituents of interest were estimated.
A focused geochemical model was presented in Appendix D of the Basis of
Design Report for the Interim Action Plan (SynTerra, 2017a). This model was
limited to the northwest corner of the ash basin.
Laboratory Determination of Distribution Coefficient
HDR retained researchers from the University of North Carolina at Charlotte
(UNCC) to determine site-specific distribution coefficients (Kd) for the primary
hydrostratigraphic units. The UNCC Soil Sorption Evaluation and Addendum to
the UNCC Soil Sorption Evaluation reports are provided in Appendix C.
Selected soil samples were analyzed using batch and column experiments to
determine Kd values for COIs (Table 13-1). In addition to these analyses, metal
oxy-hydroxide phases of iron (HFO), manganese (HMO), and aluminum (HAO)
in soils were measured. HFO, HMO, and HAO are considered to be the most
important surface reactive phases for cationic and anionic constituents in many
subsurface environments (Ford, W., & Puls, 2007). Quantities of these phases in
soil can thus be considered a proxy for the presence of ferrihydrite (HFO) and
gibbsite (HAO) which can be used to model COI sorption capacity for a given
soil (Dzombak & Morel, 1990); (Karamalidis & Dzombak, 2010).
Geochemical Model Construction
To examine the sorption behavior of multiple ions of interest in the subsurface
environment surrounding coal-fired power plants, a combined aqueous
speciation and surface complexation model was developed using the USGS
geochemical modeling program PHREEQC. Equilibrium constants for aqueous
speciation reactions were taken from the USGS WATEQ4F database. This
database contained the reactions for most elements of interest except for Co, Sb,
V, and Cr. Constants for aqueous reactions and mineral formation for these
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elements were taken from the MINTEQ v4 database which is also issued with
PHREEQC. The constants were all checked to provide a self-consistent
incorporation into the revised database. The source of the MINTEQ v4 database
is primarily the well-known NIST 46 database (Martell & Smith, 2001). Sorption
reactions were modeled using a diffuse double layer surface complexation
model. For self-consistency in the sorption model, a single database of constants
was used as opposed to searching out individual constants from literature. The
diffuse double layer model describing ion sorption to HFO and HAO by
Dzomback and Morel (1990) and Karamalidis and Dzomback (2010),
respectively, was selected for this effort.
Geochemical Controls on COI
As described in previous geochemical model reports (HDR, 2016), pH, Eh, and
solubility are the primary geochemical parameters affecting constituent mobility.
In the updated geochemical model that will be submitted in 2018 as part of the
CAP, hydraulically significant flow transects will be used to evaluate the
conceptual model of COI mobility in the subsurface. It will compare trends in the
concentrations of COIs along transects with the model output to verify that the
conceptual and qualitative models can predict COI behavior. Then the model can
be used to evaluate the potential impacts of remediation activities. The model
will relate the COI concentrations observed in groundwater along flow transects
to key geochemical parameters influencing constituent mobility (i.e., Eh, pH, and
saturation/solubility controls).
Geochemical Model Assumptions
Several key assumptions will be applied to the planned geochemical modeling
effort:
1) The thermochemical sorption constant reactions describe ion sorption
to ferrihydrite and gibbsite (HFO and HAO).
2) The model will use the same or more conservative site density
assumptions as those used by Dzombak and Morel (1990) and
Karamalidis and Dzombak (2010) to constrain the surface sites.
HAO and HFO (i.e., gibbsite and ferrihydrite) are used as the primary reactive
minerals due to the availability of surface complexation reactions. Differences
between the sorption behaviors at each site will be primarily due to 1) differences
in the pH, Eh, and ion concentrations at each site, and 2) differences in the
extractable iron and aluminum concentrations from Site specific solids.
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Additional reactive minerals will be incorporated into the model as needed on a
Site specific basis.
Updated Geochemical Model Development
The updated geochemical site investigation to accompany the CAP will develop
parameters for each aquifer or geologically derived flow zone (geozone) by
considering the bulk densities, porosities, and hydraulic gradients used in the
fate and transport model. These parameters are used to constrain the sorption
site concentrations in the model input and will be incorporated in the 1-D
ADVECTION model to accompany the capacity simulations. The objective of
these capacity simulations is to determine the mass balance on iron and
aluminum sorption sites when simulating flow through a fixed region.
Groundwater concentrations and initial solid phase iron and aluminum
concentrations will be fixed based on site-specific data. Thus, the model will be
able to simulate the stability of the HFO and HAO phases assumed to control
constituent sorption.
The updated geochemical model report will include a site specific discussion of:
The model description,
The purpose of the geochemical model,
Modeling results with comparison to observed conditions,
COI sensitivity to pH, Eh, iron/aluminum oxide content, and
Model limitations.
The updated geochemical modeling will also present multiple methods of
determining constituent mobility at the Site. Aqueous speciation, surface
complexation, and solubility controls will be presented in the revised report.
These processes will be modeled using:
Pourbaix diagrams created with the Geochemist Workbench v10 software
using site-specific minimum and maximum constituent concentrations.
PHREEQC’s combined aqueous speciation and surface complexation
model and the 1-D ADVECTION function to gain a comprehensive
understanding of current geochemical controls on the system and evaluate
how potential changes in the geochemical system might affect constituent
mobility in the future.
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Summary of Geochemical Model Results To Date 13.2.2
The relationship between aqueous and sorbed COI concentrations is an
equilibrium process. However, redox conditions vary widely across the site
indicating the site soils (ash) may not have reached equilibrium with the
groundwater which may affect the results of the model.
The geochemical model results presented in the CAP Part 2 (HDR, 2016) verified
the geochemical behavior of the constituents of interest.
Constituents found to be relatively mobile with low distribution
coefficients included barium and antimony.
Low distribution coefficients were predicted for some additional species
such as boron, cobalt, iron, manganese, and nickel.
High distribution coefficients indicating low mobility were found for
arsenic, beryllium, and chromium.
Intermediate to high distribution coefficients indicating variable to low mobility
were found for selenium, sulfate, and vanadium.
Groundwater to Surface Water Pathway Evaluation 13.3
Regulation 15A NCAC 02L requires that groundwater discharge will not possess
constituent concentrations that would result in exceedances of standards for surface
waters contained in 15A NCAC 02B .0200.
The BCSS ash basin is located south of the Dan River, and north and west of Belews
Reservoir. The Dan River represents a groundwater discharge feature for the ash basin.
Belews Reservoir represents a groundwater receptor east of the ash basin.
Dan River
Dan River samples SW-DR-U and SW-DR-D have had reported 2B exceedances of
turbidity, pH, DO, chloride, selenium, TDS, dissolved cadmium, and dissolved lead.
The 2B exceedances have all been greater than the concentrations reported in
background sample SW-DR-BG, which does not have any 2B exceedances reported.
Dan River sample SW-DR-U was collected immediately upstream of the confluence of
the ash basin designated effluent channel with the Dan River, and sample SW-DR-D
was collected immediately downstream of the confluence.
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Water samples SW-DR-1, SW-DR-2, SW-DR-3, and SW-DR-UA were collected from the
Dan River in September 2017 between background sample location SW-DR-BG and the
SW-DR-U location to refine the understanding the potential source of 2B exceedances
reported at SW-DR-U.
Exceedances of the 2B standards were not reported in any of the surface water samples
collected between SW-DR-BG and SW-DR-UA. A sample was inadvertently not
collected from SW-DR-U during the September 2017 sampling event; however it
appears that the 2B exceedances reported in SW-DR-U (and SW-DR-D) are a result of
the proximity to the designated effluent channel (outfall 003). The sampling results do
not suggest that the reported 2B exceedances in the Dan River are a result of influence
from the ash basin.
Belews Reservoir
No 2B exceedance have been reported in the samples (SW-BL-U and SW-BL-D)
collected from Belews Reservoir over the period of monitoring. Based on the available
data for the upstream and downstream Belews Reservoir samples and the known COI
distribution in groundwater the BCSS ash basin is not the source of 2B exceedances in
Belews Reservoir.
As shown on Figures 10-5 to 10-64, the extent of groundwater migration from the ash
basin at concentrations greater than background and 2L extend downgradient of the ash
basin but do not reach the Dan River or Belews Reservoir. Therefore, the surface water
data reflect contributions from sources other than groundwater migration from the ash
basin.
To help determine potential routes of exposure and receptors related to the ash basin,
additional surface water samples will be collected from Belews Reservoir and the Dan
River near the stream/river bank most likely to be impacted by potentially
contaminated groundwater discharge. The additional surface water sampling effort is
described in detail in Section 11.3.
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14.0 SITE ASSESSMENT RESULTS
Nature and Extent of Contamination 14.1
The site assessment described in the CSA presents the results of investigations required
by CAMA and 2L regulations. The ash basin pore water was determined to be a source
of impact to groundwater. The site assessment investigated the Site hydrogeology,
determined the direction of groundwater flow from the ash basin, and determined the
horizontal and vertical extent of impacts to groundwater and soil sufficient to proceed
with preparation of a CAP.
Constituents of Interest
COIs in groundwater identified as being associated with the BCSS ash basin include
antimony, arsenic, barium, beryllium, boron, cadmium, chloride, chromium, hexavalent
chromium, cobalt, iron, manganese, molybdenum, pH, selenium, strontium, sulfate,
thallium, TDS, and vanadium. COIs migrate laterally and vertically into and through
regolith, the transition zone, and shallow bedrock. Constituent migration in
groundwater occurs at variable rates depending on constituent sorption properties and
geochemical conditions (e.g., redox state, pH, etc.). Some COIs, such as boron, readily
solubilize and migrate with minimal retention. In contrast, some COIs such as arsenic
readily adsorb to aquifer materials, do not readily solubilize, and thus are relatively
immobile.
Hydrogeologic Conditions
Site hydrogeologic conditions were evaluated by installing and sampling groundwater
monitoring wells; conducting in-situ hydraulic tests; sampling soil for physical and
chemical testing; and sampling surface water, AOW, and sediment samples. Monitoring
wells were completed in each hydrostratigraphic unit. The groundwater flow system
serves to store and provide a means for groundwater movement. The porosity of the
regolith is largely controlled by pore space (primary porosity); whereas, in bedrock, the
effective porosity is largely secondary and controlled by the number, size, and
interconnection of fractures. The nature of groundwater flow across the Site is based on
the character and configuration of the ash basin relative to specific Site features such as
manmade and natural drainage features, engineered drains, streams, and lakes;
hydraulic boundary conditions; and subsurface media properties. The groundwater
flow across the Site appears to flow through the interconnected flow layers.
Four hydrostratigraphic layers were identified at the BCSS and were evaluated during
the CSA:
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Ash – The ash pore water unit consists of saturated ash material. Observed ash
depths range from a few feet to approximately 66 feet.
Shallow – The shallow flow layer consists of soil and saprolite material that
overlie the transition zone and bedrock. Alluvial deposits were not encountered
in any of the boreholes in the area of the BCSS ash basin. Where present, the first
occurrence of groundwater is generally represented by this layer.
Deep (Transition Zone) – The deep (TZ) flow regime is a relatively transmissive
zone of partially weathered bedrock comprised of rock fragments,
unconsolidated material, and highly oxidized bedrock. This unit lies directly
above competent bedrock; although, the change of transition zone material into
bedrock can be indistinct and characterized by subtle differences in secondary
mineralization, weathering, rock quality/competency, and fracture density.
Fractured Bedrock – Secondary porosity through weathering and subsequent
fracturing of bedrock control groundwater flow through the deepest
hydrostratigraphic unit beneath BCSS. Water-bearing fractures are minimally
productive.
The BCSS ash basin acts as a bowl-like feature towards which groundwater flows from
the basin to the east, northeast, north, and northwest. Groundwater primarily flows
north toward the Dan River. Groundwater at the Site flows away from the topographic
and hydrologic divide (highest topographic portion of the Site) generally located along
Pine Hall Road to the north and south. The flow of ponded water within the ash basin
is controlled laterally by groundwater flow that enters the basin from the south and is
controlled downgradient (north) by the ash basin main dam and the NPDES
outfall/discharge. The head created by the ash pore water creates a slight mounding
effect that influences the groundwater flow direction in the immediate vicinity of the
ash basin.
In summary, there are no substantive differences in water level among wells completed
in the different flow zones across the Site (shallow; deep; bedrock), and generally lateral
groundwater movement predominates over vertical movement. The vertical gradients
are near equilibrium across the Site indicating that there is no distinct horizontal
confining layer beneath the Site. The horizontal gradients, hydraulic conductivity, and
seepage velocities indicate that most of the groundwater transport occurs through the
transition zone and bedrock, as most of the regolith encountered downgradient of the
basin is thin and less likely to be saturated.
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Groundwater flow directions and the overall morphology of the potentiometric surface
vary little from “dry” to “wet” seasons. Water levels do fluctuate up and down with
significantly increased or decreased precipitation, but the overall groundwater flow
direction does not change due to seasonal changes in precipitation. Horizontal
gradients in the ash basin range from 0.002 to 0.006 ft/ft. The ash basin gradients are low
compared to downgradient areas likely due to the low relief in the basin. Horizontal
gradients along the southern portion of the Site downgradient of the topographic ridge
are highest (0.035 ft/ft). The gradient is influenced by the steep relief in the southern
portion of the property as the area slopes down to Belews Reservoir. Horizontal
gradients along the north, northwest end of the Site range from 0.004 to 0.025 ft/ft. The
hydraulic gradient in the northern portion of the Site is influenced by the higher relief
between this area and the ash basin dam. Vertical gradients in saprolite, transition zone
and bedrock wells are near equilibrium, indicating that there is no distinct horizontal
confining layer beneath BCSS. Generally, upward vertical gradients predominate on
the northeast and south side of the Site near Belews Reservoir, and include areas of the
ash basin for deep and bedrock zones, while downward (recharge) gradients are more
prevalent in the north and northwest portion of the property.
Horizontal and Vertical Extent of Impact
Boron is a CCR-derived constituent in groundwater and is detected at concentrations
greater than the NC 2L standard beneath the ash basin and the Pine Hall Road Landfill
and downgradient of the ash basin (north and northwest). Boron is not detected in
background groundwater. Boron, in its most common forms, is soluble in water, and
boron has a very low Kd value, making the constituent highly mobile in groundwater.
Therefore, the presence/absence of boron in groundwater provides a close
approximation of the distribution of CCR-impacted groundwater. The detection of
boron at concentrations in groundwater greater than applicable 2L standards and
PBTVs best represents the leading edge of the CCR-derived plume moving
downgradient from the source area (ash basin and Pine Hall Road Landfill).
As previously described, the groundwater plume is defined as any locations (in three-
dimensional space) where groundwater quality is impacted by the ash basin. Naturally
occurring groundwater contains varying concentrations of alkalinity, aluminum,
bicarbonate, cadmium, carbonate, copper, lead, magnesium, methane, nickel,
potassium, sodium, total organic carbon (TOC), and zinc. Sporadic and low-
concentration exceedances of these constituents in the groundwater data do not
necessarily demonstrate horizontal or vertical impacts from the ash basin. The leading
edge of the plume, the farthest downgradient edge, is represented by groundwater
concentrations in the wells in each flow layer. In the bedrock flow layer, boron is
reported in downgradient well MW-200BR, located north of the ash basin main dam at
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the compliance boundary at a concentration greater than the PBTV and less than the 2L
standard. Further downgradient boron has not been detected in wells MW-24D/BR.
Boron is also detected in the bedrock flow layer at monitoring well GWA-20BR, located
northwest of the ash basin at a concentration greater than the PBTV and less than the 2L
standard. Boron is also detected in the bedrock flow layer at monitoring well OB-9,
located north/northwest of the Pine Hall Road Landfill at a concentration greater than
the PBTV and less than the 2L standard. The leading edge of the bedrock boron plume
is interpreted to be at or just beyond these monitoring wells. The remaining bedrock
downgradient wells did not have boron detected.
In the deep flow layer (transition zone), boron results in the monitoring wells located
within the compliance boundary on the east and southeast sides of the ash basin are
non-detect. On the north side of the ash basin boron is reported in downgradient well
MW-200D, located north of the ash basin main dam at the compliance boundary at a
concentration greater than the PBTV and less than the 2L standard. Northwest of the
ash basin, boron is reported at a concentration greater than the 2L standard at
monitoring well GWA-27D located beyond the compliance boundary. Monitoring wells
installed for other regulatory programs have added additional details about the
orientation and extent of the downgradient plume and have helped refine an
understanding of the distribution of the plume. The boron concentrations reported in
monitoring wells GWA-10DA, GWA-31D, and GWA-30D are non-detect. These wells
are located beyond GWA-21D and the leading edge of the boron plume is expected to
be generally between GWA-27D and this set of wells. Boron results exceed the 2L
standard beneath the Pine Hall Road Landfill in the deep flow layer, but are non-detect
at the compliance boundary.
The leading edge of the boron plume in the shallow flow layer east of the ash basin is
generally at the compliance boundary. North of the ash basin main dam and northwest
of the ash basin, the boron plume in the shallow flow layer extends to beyond the
compliance boundary. The boron concentration is non-detect in monitoring wells
GWA-30S and GWA-31S which define the leading edge of the boron plume in the
shallow flow layer. West of the ash basin the boron concentrations are non-detect or
less than the PBTV at the compliance boundary. Surface water samples north of the
basin from AOWs S-10 and S-11 show boron concentrations above the 2L standard,
ranging 4,960 to 10,800 µg/L. Nearby wells MW-200S/D/BR have boron detected below
the 2L standard. The boron concentration is non-detect in surface waters northwest of
the basin (AOWs S-1, S-3 through S-5), however S-2 has boron detected below the 2L
standard. Upgradient of S-2, wells GWA-31S/D have no detections of boron but further
upgradient wells GWA-19S/D/BR shows boron detected only in the shallow layer and
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above the 2L standard. Wells GWA-21S/D, upgradient of S-3 and S-4, shows boron
detected below the 2L standard and wells GWA-30S/D, upgradient of S-5, have no
detections of boron.
Beryllium, chloride, chromium, cobalt, manganese, and thallium are also constituents
detected in groundwater greater than background and 2L/IMAC near or beyond the
compliance boundary. The interpreted extent of beryllium concentrations greater than
background and the IMAC is beyond the compliance boundary in the shallow and deep
flow layers. Beryllium was not reported at a concentration greater than the IMAC in the
bedrock flow layer. The interpreted extent of chloride concentrations greater than 2L at
and beyond the compliance boundary is in the shallow and deep flow layers. Chloride
was not reported at a concentration greater than 2L in the bedrock flow layer. The
interpreted extent of chromium concentrations greater than 2L at and beyond the
compliance boundary is in the shallow and deep flow layers. Chromium was not
reported at a concentration greater than 2L in the bedrock flow layer. The interpreted
extent of cobalt concentrations greater than IMAC at and beyond the compliance
boundary is in the shallow flow layer only. Cobalt exceedances were not reported in
the deep and bedrock flow layers. The interpreted extent of manganese concentrations
greater than 2L at and beyond the compliance boundary is in the shallow, deep, and
bedrock flow layers. The interpreted extent of thallium concentrations greater than the
IMAC at and beyond the compliance boundary is in the shallow and deep flow layers.
Thallium was not reported at a concentration greater than 2L in the bedrock flow layer.
The bedrock aquifer is generally the source of water for supply wells in the area. As
outlined above, the bedrock aquifer has not been impacted by CCR constituent
migration from the ash basin with the exception of a grout contaminated well beneath
the ash basin main dam. The manganese concentrations reported in bedrock
groundwater are likely due to natural geochemical conditions.
The surficial and transition zone flow units at Belews Creek— beneath and
downgradient of the ash basin — are impacted by CCR-derived constituents; however,
these units are not vertically extensive. Impact to the bedrock flow unit beneath the
basin is observed, approximately, to the top 50 – 60 feet of fractured bedrock. The
vertical extent of the plume is represented by groundwater concentrations in bedrock
wells beneath and downgradient of the ash basin. AB-4BR, drilled to a depth of 144 feet
bgs, contains no boron or manganese concentrations above 2L or the PBTV. However
AB-9BR, drilled to 137 feet bgs has same absence of boron but has manganese detected
above the 2L. Groundwater in the transition zone beneath the basin is impacted.
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As groundwater under the ash basin flows north, northwest toward the ash basin dam,
the hydraulic impact of the ash basin dam and the hydraulic head exerted by the ash
basin water forces groundwater downward into the bedrock, which increases hydraulic
pressure in the bedrock aquifer. Wells completed in surficial, transition zone, and
bedrock proximate to the north and northwest side of the ash basin dam are impacted
by COIs. As groundwater and the plume migrate in the downgradient direction north
of the basin, unimpacted groundwater enters the system from upgradient recharge
areas to the west and east mitigating the concentration of some COIs (e.g., boron).
Boron is present in groundwater downgradient of the ash basin on the Site in
concentrations that exceed the 2L in both the shallow and transition zones. In bedrock
boron is detected at only MW-200BR, based on data from wells positioned
downgradient from the ash basin and off the Site property. Concentrations are below 2L
for this location. Surface water flowing off the Site property north and northwest of the
basin through AOWs S-2, S-10 and S-11 contain boron above 2L. The concentrations of
boron at these locations have stayed relatively stable the past two years.
Maximum Constituent Concentrations 14.2
Changes in COI concentrations over time are included as time-series graphs (Figures
14-1 through Figure 14-76). The maximum historical detected COI concentrations in
groundwater for ash pore water or wells directly beneath the ash basin and non-ash
basin groundwater are included below:
Antimony – Ash Basin: 12.3 µg/L (AB-08SL); Outside Basin: 98,500 µg/L (OB-4)
Arsenic – Ash Basin: 494 µg/L (AB-08SL); Outside Basin: 91.8 µg/L (OB-4)
Barium – Ash Basin: 348 µg/L (AB-08SL); Outside Basin: 836 µg/L (GWA-19SA)
Boron - Ash Basin: 21,900 µg/L (AB-04S); Outside Basin: 44,600 µg/L (OB-4)
Beryllium - Ash Basin: 0.24 µg/L (AB-04S); Outside Basin: 11.5 µg/L (GWA-11S)
Chloride– Ash Basin: 884 µg/L (AB-7S); Outside Basin: 499 µg/L (GWA-20SA)
Cadmium – Ash Basin: 1.9 µg/L (AB-7S); Outside Basin: 18.72 µg/L (OB-4)
Chromium – Ash Basin: 15.8 µg/L (AB-1S); Outside Basin: 269 µg/L (GWA-3S)
Chromium (hexavalent) – Ash Basin: 5.5 µg/L (AB-08SL); Outside Basin: 8.3
µg/L (GWA-23D)
Cobalt – Ash Basin: 271 µg/L (AB-7S); Outside Basin: 413 µg/L (MW-102S)
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Iron – Ash Basin: 137,000 µg/L (AB-08SL); Outside Basin: 92,200µg/L (MW-103S)
Manganese – Ash Basin: 15,400 µg/L (AB-2D); Outside Basin: 2,300 µg/L (MW-
102S)
Molybednum – Ash Basin: 3,460 µg/L (AB-4SL); Outside Basin: 22.3 µg/L (GWA-
6D)
pH - Ash Basin: 3.9 (AB-7S) – 11.5 (AB-4SL); Outside Basin: 4.1 (GWA-10S) – 8.8
(GWA-20BR)
Nickle – Ash Basin: 174 µg/L (AB-7); Outside Basin: 139 µg/L (GWA-3S)
Radium (combined 226+228): 9.11 pCi/L (AB-2D); Outside Basin: 11.91 pCi/L
(GWA-10S)
Selenium - Ash Basin: 205 µg/L (AB-7S); Outside Basin: 401 µg/L (OB-9)
Strontium - Ash Basin: 5,600 µg/L (AB-5SL); Outside Basin: 1,040 µg/L (GWA-
20D)
Sulfate – Ash Basin: 637 mg/L (AB-7S); Outside Basin: 1,746 mg/L (OB-4)
TDS – Ash Basin: 2,430 mg/L (AB-5SL); Outside Basin: 2,839 mg/L (OB-4)
Thallium – Ash Basin: 5.5 µg/L (AB-8S); Outside Basin: 25.8 µg/L (OB-4)
Vanadium – Ash Basin: 948 µg/L (AB-4S): Outside Basin: 213 µg/L (OB-4)
Exceedances of PBTV soil concentrations are limited to only a few locations outside of
the footprint of the ash basin. Concentrations of arsenic exceeding the PBTV are
concentrated in areas north of the ash basin (GWA-1 and GWA-2) and northwest of the
ash basin (GWA-9, GWA-10 and GWA-11). A few locations have iron concentrations
that exceed the PBTV but appear spatially inconsistent beyond the ash basin footprint.
Contaminant Migration and Potentially Affected Receptors 14.3
Contaminant Migration
The groundwater flow system at the Site serves both to store and provide a means for
groundwater movement. The porosity of the regolith is largely controlled by pore
space (primary porosity), whereas in bedrock, porosity is largely controlled by the
number, size, and interconnection of fractures. As a result, the effective porosity in the
regolith is normally greater than in the bedrock and thus the quantity of groundwater
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flow will be greater in the regolith. At the Site, all hydrogeologic zones are saturated,
however downgradient of the basin closer to the Dan River the regolith is observed to
become thinner and less saturated (MW-24S). Across the site the regolith is the least
transmissive of the flow zones. The majority of groundwater across the Site appears to
flow through the transition zone and bedrock.
Figures 14-77 to 14-96 show the most recent COI groundwater analytical concentrations
for CAMA monitoring wells. The figures are color-coded to visually depict whether
analytical concentrations are increasing, decreasing, stable, or a trend could not be
determined. The vast majority of figures show concentrations for most COIs are stable,
with a few notable exceptions. Figures 14-81 and 14-92 show concentrations of boron
and strontium increasing downgradient, northwest of the ash basin. For boron,
concentrations are increasing in monitoring wells screened in the shallow zone and
transition zone, downgradient of the ash basin. Figures 14-79 and 14-80 show similar
temporal trends between barium and beryllium, with increasing concentrations north,
northwest of the ash basin. Figure 14-87 and 14-88 show iron and manganese
decreasing in many wells downgradient and outside of the ash basin across the site,
which could be attributable to the wells stabilizing after a period of time has passed
since well installation.
The pore water in the ash basin is the source of constituents detected above 2L in
groundwater samples in the vicinity of the ash basin. Gradients measured within the
ash basin support the interpretation that ash pore water mixes with shallow/surficial
groundwater and migrates downward into the transition zone. Continued vertical
migration of groundwater downgradient of the ash basin is also evidenced by detected
constituent concentrations. Ash basin constituents become dissolved in groundwater
that flows north, northwest in response to hydraulic gradients, with potential mixing of
source area groundwater and regional groundwater along side-gradients east and west
of the ash basin. Groundwater migrates under diffuse flow conditions in the surficial
aquifer in the direction of the prevailing gradient. As constituents enter the transition
zone and fractured bedrock flow systems, the rate of constituent transport has the
potential to increase. Groundwater flow is the primary mechanisms for migration of
constituents to the environment.
The hydrogeologic characteristics of the ash basin environment are the primary control
mechanisms on groundwater flow and constituent transport. The basin acts as a bowl-
like feature toward which groundwater flows from all directions except from the north.
The valley in which the ash basin was constructed follows the slope-aquifer system,
where flow of groundwater into the ash basin and out of the ash basin is restricted to
the local flow regime. Shallow groundwater and surface water flow from the ash basin
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is funneled into a natural valley with engineered structures to capture northerly flow
from the dam and eventually discharges into the Dan River as a permitted outfall.
Groundwater also flows northwest from the ash basin into several natural valleys
which also flow to the north of the property discharging into the Dan River. Boron is
present in groundwater in both the north and northwest valleys extending from the ash
basin at concentrations that exceed the 2L. Downgradient of the ash basin to the
northwest, boron concentrations above 2L extend outside the compliance boundary.
At BCSS, groundwater movement in the bedrock flow zone is due primarily to
secondary porosity represented by fractures in the bedrock. Primary (matrix) porosity
is negligible; therefore, it is not technically appropriate to calculate groundwater
velocity using effective porosity values and the method presented above. Bedrock
fractures encountered at Belews Creek tend to be isolated with low interconnectivity.
Further, hydraulic conductivity values measure the fractures immediately adjacent to a
well screen, not across the distance between two bedrock wells. Groundwater flow in
bedrock fractures is anisotropic and difficult to predict, and velocities change as
groundwater moves between factures of varying orientations, gradients, pressure, and
size.
Recent concentrations of COIs in groundwater, surface water, and AOWs are provided
on Figures 14-97 and 14-98. Recent concentrations of COIs in solid media, as well as
available geochemical properties of soils and sediments, are provided on Figure 14-99.
Potentially Affected Receptors
A baseline human health and ecological risk assessment was performed in 2016. An
update to the risk assessment has been completed (Section 12.0). The update evaluated
recent analytical data for their potential to influence 2016 risk assessment conclusions.
Human
The 2016 risk assessment estimated potential risks under a hypothetical subsistence
fisher scenario exposed to thallium and cobalt in fish tissue modeled from surface water
concentrations, and potential risks from thallium under a hypothetical recreational
fisher scenario. The risks were likely overestimated because of very conservative
assumptions in the exposure models. Concentrations of cobalt and thallium have
decreased in subsequent sampling events and have not exceeded the respective human
health screening levels of 1 µg/L (cobalt) and 0.2 µg/L (thallium) in the two most recent
sampling events at SW-DR-U. Thus, there is no evidence of potential risks under the
hypothetical fisher scenario from exposure to cobalt and thallium.
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Ecological
One surface water sample location was included in the assessment for Ecological
Exposure Area 3: SW-BL-D in Belews Reservoir . A new maximum concentration of
cobalt did not result in a wildlife hazard quotient greater than unity (1); therefore there
is no evidence of risks to ecological receptors exposed to cobalt at the SW-BL-D sample
location. In addition, Belews Reservoir is considered beyond the extent of constituent
migration in groundwater from the ash basin.
Water Supply Wells
Concentrations of analyzed constituents exceeded the respective PBTVs for a number of
private water supply wells; however, these data should be interpreted with caution for
the reasons described below:
There is very limited information available about the sampled wells. It is likely
the wells were constructed as open-hole bedrock wells.
Groundwater geochemistry in fractured bedrock aquifers can be quite variable.
PBTVs were developed using groundwater data from a set of two background
monitoring wells all located on the Site. The geochemical data from these wells
may not be representative across the broader area encompassed by the 50 private
water supply wells and one public water supply well.
Well construction, pump, piping, and well materials may influence analytical
results.
A numerical capture zone analysis for the BCSS Site was conducted to evaluate
potential impact of upgradient water supply pumping wells. None of the particle
tracks originating in the ash basin moved into the well capture zones.
Based on the bedrock groundwater flow direction at the site (Figures 6-10 and 6-11,
discussed in Section 6.3) private water supply wells located west of the ash basin along
Old Plantation Road (WSWs samples BC2019-RAW, BC2 Well 1, BC2 Well 2, BC-1007,
BC4, BC4A and BC4B) are located sidegradient of the ash basin. The remaining water
supply wells are located in upgradient or a sufficient distance sidegradient to not be
impacted by groundwater migration from the ash basin.
Analytical data is not available for water supply well BC4. The turbidity reading in BC4
Well B at the time of sampling was 19.3 NTU, therefore the data is not considered valid,
and is not evaluated.
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Iron was reported at concentrations which exceed the bedrock PBTV (228 µg/L) and the
2L standard (300 µg/L) in water supply well samples BC-1007, BC2 Well 1, BC2 Well 2,
and BC2019-RAW. However, the iron concentrations in these water supply wells are
within the background concentration range for similar Piedmont geologic settings.
Vanadium was reported at a concentration greater than the IMAC but less than the
bedrock PBTV in water supply well sample BC2019-RAW, and greater than the IMAC
and PBTV in BC4 Well A. However, the vanadium concentrations in these water
supply wells are within the background concentration range for similar Piedmont
geologic settings.
Boron was not detected in any of these water supply wells sampled sidegradient of the
ash basin.
A Piper diagram for water supply well data compared to ash basin pore water,
background bedrock monitoring wells and bedrock monitoring wells located
downgradient of the ash basin (between the ash basin and the private water supply
wells) is presented as Figure 4-3. Observations based on the diagram include:
Water supply wells are characterized as calcium bicarbonate water type,
consistent with samples collected from the background bedrock well at BCSS.
Monitoring well MW-203BR (located between the ash basin and the private
water supply wells to the west) plots along with background well BG-2BR,
indicating this well is likely representative of unimpacted groundwater.
Monitoring well GWA-9BR (located between the ash basin and the private water
supply wells to the west) plots between calcium-magnesium sulfate type water
and calcium bicarbonate water, a result of the concentration of chloride (52.7
mg/L) relative to the concentration of sulfate and may indicate potential mixing
with source area groundwater.
The signature of the water supply wells is similar to the background bedrock well at the
site indicating that these wells are not impacted by the source area water.
Surface Waters
As shown Figures 10-5 to 10-64, the extent of groundwater migration from the ash basin
at concentrations greater than background and 2L extend downgradient of the ash basin
but do not reach the Dan River or Belews Reservoir. Therefore, the surface water data
reflect contributions from sources other than groundwater migration from the ash
basin.
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In the Dan River, exceedances of the 2B standards were not reported in any of the
surface water samples collected between SW-DR-BG and SW-DR-UA. A sample was
inadvertently not collected from SW-DR-U during the September 2017 sampling event,
however it appears that the 2B exceedances reported in SW-DR-U (and SW-DR-D) are a
result of the proximity to the designated effluent channel (outfall 003). The sampling
results do not suggest that the reported 2B exceedances in the Dan River are a result of
influence from the ash basin.
No 2B exceedance have been reported in the samples (SW-BL-U and SW-BL-D)
collected from Belews Reservoir over the period of monitoring. Based on the available
data for the upstream and downstream Belews Reservoir samples the BCSS ash basin is
not the source of 2B exceedances Belews Reservoir.
To help determine potential routes of exposure and receptors related to the ash basin,
additional surface water samples will be collected from Belews Reservoir and the Dan
River near the stream/river bank most likely to be impacted by potentially
contaminated groundwater discharge. The additional surface water sampling effort is
described in detail in Section 11.3.
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15.0 CONCLUSIONS AND RECOMMENDATIONS
A discussion of preliminary corrective action alternatives that may be appropriate to
consider during the updated CAP development are presented in this section.
Overview of Site Conditions at Specific Source Areas 15.1
The horizontal and vertical extent of exceedances has been defined (Figure ES-1)
sufficiently for preparation of the CAP. Boron exceedances in the shallow flow layer are
primarily located north of the ash basin main dam, within the compliance boundary,
and northwest of the ash basin, at or beyond the compliance boundary. In the deep
flow layer boron exceedances are located beneath the ash basin and the Pine Hall Road
Landfill, north of the ash basin main dam, within the compliance boundary, and
northwest of the ash basin, at or beyond the compliance boundary. Boron exceedances
are also reported south of the topographic divide along Pine Hall Road, west of the
structural fill. These exceedances are not related to the ash basin and a separate
assessment of the structural fill is ongoing. There are no boron exceedances reported in
the bedrock flow layer in monitoring wells that are not grout contaminated (high pH).
Beryllium, chloride, chromium, cobalt, manganese, and thallium are also constituents
detected in groundwater greater than background and 2L/IMAC near or beyond the
compliance boundary. The interpreted extent of beryllium concentrations greater than
background and the IMAC is beyond the compliance boundary in the shallow and deep
flow layers. Beryllium was not reported at a concentration greater than the IMAC in the
bedrock flow layer. The interpreted extent of chloride concentrations greater than 2L at
and beyond the compliance boundary is in the shallow and deep flow layers. Chloride
was not reported at a concentration greater than 2L in the bedrock flow layer. The
interpreted extent of chromium concentrations greater than 2L at and beyond the
compliance boundary is in the shallow and deep flow layers. Chromium was not
reported at a concentration greater than 2L in the bedrock flow layer. The interpreted
extent of cobalt concentrations greater than IMAC at and beyond the compliance
boundary is in the shallow flow layer only. Cobalt exceedances were not reported in
the deep and bedrock flow layers. The interpreted extent of manganese concentrations
greater than 2L at and beyond the compliance boundary is in the shallow, deep, and
bedrock flow layers. The interpreted extent of thallium concentrations greater than the
IMAC at and beyond the compliance boundary is in the shallow and deep flow layers.
Thallium was not reported at a concentration greater than 2L in the bedrock flow layer.
The bedrock aquifer is generally the source of water for supply wells in the area. As
outlined above, the bedrock aquifer has not been impacted by CCR constituent
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migration from the ash basin. The manganese concentrations reported in bedrock
groundwater are likely due to natural geochemical conditions.
In ash basin locations where soil samples were collected beneath the ash, analytical
results indicate arsenic and selenium concentrations greater than PBTVs and PSRGs for
POG are present. Strontium was also reported in five of the soil samples collected
beneath the ash basin at concentrations greater than the background concentration.
There is no PSRG POG for strontium. No other COIs were detected in soil beneath the
ash basin at concentrations greater than PBTVs or PSRG POGs.
Revised Site Conceptual Model 15.2
Site Conceptual Models (SCMs) are developed to be a representation of what is known
or suspected about a site with respect to contamination sources, release mechanisms,
transport, and fate of those contaminants. SCMs can be a written and/or be a graphic
presentation of site conditions to reflect the current understanding of the site, identify
data gaps, and be updated as new information is collected throughout the project.
SCMs can be utilized to develop understanding of the different aspects of site
conditions, such as a hydrogeologic conceptual site model, to help understand the site
hydrogeologic condition affecting groundwater. SCMs can also be used in a risk
assessment to understand contaminant migration and pathways to receptors.
In the initial site conceptual hydrogeologic model presented in the Work Plan dated
December 30, 2014, the geological and hydrogeological features influencing the
movement, chemical, and physical characteristics of contaminants were related to the
Piedmont hydrogeologic system present at the site. A SCM was developed from data
generated during previous assessments, existing groundwater monitoring data, and
CSA activities.
The BCSS ash basin is located in the central part of the BCSS site and receives surface
water runoff and groundwater recharge from upland areas south of the basin.
Assessment results indicate the thickness of CCR in the ash basin ranges from a few feet
to approximately 66 feet. Assessment findings determined that pore water in the ash
basin is the primary source of impact to groundwater. As previously discussed, residual
concentrations of arsenic, selenium and strontium in soil beneath the ash basin may also
represent a secondary source.
The ash basin discharges pore water to the subsurface beneath the basin. Groundwater
from the ash basin flows downgradient of the ash basin dam predominately through
the designated effluent channel, discharging to the Dan River (NPDES outfall 003).
Groundwater in the vicinity of the ash basin also flows to the northwest towards the
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Dan River and to the east towards Belews Reservoir. Horizontal migration of
groundwater at the site is generally controlled by topographic divides along Pine Hall
Road to the south and east of the ash basin and along Middleton Loop Road to the west
of the ash basin. These topographic divides generally function as groundwater divides,
although groundwater flow across topographic divides may be possible based on
hydraulic head conditions from the ash basin and the existence of preferential flow
paths within the shallow and/or deep flow layers.
The horizontal and vertical extent of exceedances has been sufficiently defined for
preparation of the updated CAP. Seventeen constituents were reported at
concentrations greater than their corresponding background concentration range, 2L or
IMACs in one or more pore water samples. In groundwater, the maximum COI
concentrations occur in the shallow and deep flow layers. The maximum concentrations
are located northwest, downgradient of the ash basin. Concentrations of boron, cobalt,
iron, manganese, sulfate, TDS are also observed west of the Structural Fill. The extent of
constituent migration in groundwater at concentrations greater than site background
and groundwater quality standards is shown on Figure ES-1.
Boron and additional COI exceedances in the shallow and deep flow layers are
primarily located north of the ash basin main dam, within the compliance boundary,
and northwest of the ash basin, at or beyond the compliance. The bedrock aquifer is
generally the source of water for supply wells in the area. As outlined above, the
bedrock aquifer has not been impacted by CCR constituent migration from the ash
basin. The manganese concentrations reported in bedrock groundwater are likely due
to natural geochemical conditions.
Constituent concentrations in bedrock groundwater directly downgradient of the ash
basin are less than 2L with the exception of manganese, which appears to be due to
geochemical conditions. The water chemistry signature of the water supply wells is
similar to the background bedrock wells at the site. Although several water supply well
concentrations reported are greater than the site specific PBTVs, the concentrations are
within the background concentration range for similar Piedmont geologic settings.
Monitoring wells GWA-19BR, GWA-20BR, and GWA-27BR are located northwest of the
ash basin. These wells are grout contaminated (high pH) and their data is not
considered valid. The boron concentrations reported in these monitoring wells are
similar to the boron background concentration.
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As shown Figures 10-5 to 10-64, the extent of groundwater migration from the ash basin
at concentrations greater than background and 2L extend downgradient of the ash basin
but do not reach the Dan River or Belews Reservoir. Therefore, the surface water data
reflect contributions from sources other than groundwater migration from the ash
basin.
The ecological risk assessment considered surface water data associated with Belews
Reservoir beyond the extent of constituent migration in groundwater from the ash
basin. As such, the findings for the Belews Reservoir do not imply adverse effects
associated with groundwater to surface water migration from the ash basin. This
exposure route will be further evaluated through direct surface water sampling and
predictive modeling as part of the CAP. To date, 2B and EPA water quality criteria
have not been exceeded in waters proximal to areas of groundwater impact.
The SCM will continue to be refined following evaluation of the completed
groundwater model in the CAP and additional information obtained in subsequent data
collection activities.
Interim Monitoring Program 15.3
An Effectiveness Monitoring Program (EMP) is required by CAMA §130A-309.209
(b)(1)e. The EMP for BCSS will begin once the basin closure and groundwater CAP
have been implemented. In the interim, and Interim Monitoring Plan (IMP) has been
developed at the direction of NCDEQ. The IMP is designed to monitor near-term
groundwater quality changes. The CAP, and a proposed EMP, will be submitted at a
future date; therefore, this section presents details of the IMP only.
IMP Implementation 15.3.1
An IMP has been implemented in accordance with NCDEQ correspondence
(NCDEQ, October 19, 2017) that provided an approved “Revised Interim
Monitoring Plans for 14 Duke Energy Facilities” (Appendix A). Sampling will be
conducted quarterly until approval of the CAP or as otherwise directed by
NCDEQ. These events will be conducted in conjunction with the NPDES
triennial monitoring with a fourth sampling event added to provide four rounds
of sampling during the year. Groundwater samples will be collected using low-
flow sampling techniques in accordance with the Low Flow Sampling Plan, Duke
Energy Facilities, Ash Basin Groundwater Assessment Program, North Carolina, June
10, 2015 (Appendix G) conditionally approved by NCDEQ in a June 11, 2015
email with an attachment summarizing their approval conditions.
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Samples will be analyzed by a North Carolina certified laboratory for the
parameters listed in Table 15-1. The table includes targeted minimum detection
limits for each listed constituent. Analytical parameters and detection limits for
each media were selected so the results could be used to evaluate the
effectiveness of a future remedy, conditions within the aquifer that may
influence the effectiveness of the remedy, and migration of constituents related
to the ash basin. Laboratory detection limits for each constituent are targeted to
be at or below applicable regulatory values (i.e., 2L, IMAC, or 2B).
Monitoring wells and surface water locations that will be sampled and
monitored as part of the IMP, as approved in NCDEQ correspondence (NCDEQ,
October 19, 2017; Appendix A), are included in Table 15-2.
IMP Reporting 15.3.2
Currently, data summary reports comprised of analytical results received during
the previous month are submitted to NCDEQ on a monthly basis. In addition,
NCDEQ (May 1, 2017) directed that an annual IMP report be submitted by April
30 of the following year of data collection. The reports shall include materials
that provide “an integrated, comprehensive interpretation of site conditions and
plume status.” The initial IMP Report is to be submitted to NCDEQ no later than
April 30, 2018.
Preliminary Evaluation of Corrective Action Alternatives 15.4
Closure of the ash basin is required by 2024 under CAMA (Intermediate Risk). The
updated risk assessment (Section 12.0) has determined there are indications that
potential risks to humans and wildlife at the Belews Creek site. Risk calculations using
new results will be required to estimate potential risks posed by newly detected
constituents and constituents detected at greater concentrations since completing the
2016 risk assessment. Groundwater in the bedrock flow unit, typically used for private
drinking water supply wells in the region, is impacted. In locations beneath the ash
basin where soil samples could be collected, analytical results indicate shallow impacts
of COIs above PBTVs. If needed, groundwater and surface water can be remediated
over time using a variety of approaches and technologies. The updated groundwater
model (presented in Appendix C of the Basis of Design Report for the Interim Action
Plan (SynTerra, 2017)) predicts that ten extraction wells within the transition zone
(model layer 6) will lower groundwater levels for more than 5 to 10 feet along the
extraction system axis, with hydraulic impacts to northwest corner of the ash basin.
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Site wide simulation data for the updated model extended out until such time as
compliance with 2L at the compliance boundary is achieved will be presented in the
updated CAP.
This preliminary evaluation of corrective action alternatives is included to provide
insight into the groundwater CAP preparation process. This preliminary evaluation is
based on data available and the current understanding of regulatory requirements for
the Site. It is assumed a source control measure of either capping the ash basin and
minimizing infiltration, or excavation, or a combination of the two, will be designed
following completion of the risk classification process. The groundwater currently
presents minimal, if any, risk to receptors. A low risk classification and closure via a
cap-in-place scenario are considered viable. Potential groundwater remedial strategies
are being considered as part of the closure design, in addition to the groundwater
extraction system currently being installed.
CAP Preparation Process 15.4.1
The CAP preparation process is designed to identify, describe, evaluate, and
select remediation alternatives. Those alternatives will have the objective of
bringing groundwater quality to levels that meet applicable standards, to the
extent that the objective is economically and technologically feasible, in
accordance with 2L .0106 Corrective Action. Sections (h), (i), and (j) regarding
CAP preparation read as follows:
(h) Corrective action plans for restoration of groundwater quality, submitted pursuant
to Paragraphs (c), (d), and (e) of this Rule shall include:
(1) A description of the proposed corrective action and reasons for its selection;
(2) Specific plans, including engineering details where applicable, for restoring
groundwater quality;
(3) A schedule for the implementation and operation of the proposed plan; and
(4) A monitoring plan for evaluating the effectiveness of the proposed corrective
action and the movement of the contaminant plume.
(i) In the evaluation of corrective action plans, the Secretary shall consider the extent
of any violations, the extent of any threat to human health or safety, the extent of
damage or potential adverse impact to the environment, technology available to
accomplish restoration, the potential for degradation of the contaminants in the
environment, the time and costs estimated to achieve groundwater quality
restoration, and the public and economic benefits to be derived from groundwater
quality restoration.
(j) A corrective action plan prepared pursuant to Paragraphs (c), (d), or (e) of this
Rule shall be implemented using a remedial technology demonstrated to provide the
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most effective means, taking into consideration geological and hydrogeological
conditions at the contaminated site, for restoration of groundwater quality to the
level of the standards. Corrective action plans prepared pursuant to Paragraphs (c)
or (e) of this Rule may request an exception as provided in Paragraphs (k), (l), (m),
(r), and (s) of this Rule.
To meet these requirements and to provide a comprehensive evaluation, it is
anticipated that the complete CAP will include:
Descriptions of site conditions
Corrective action objectives and evaluation criteria
Technology assessment
Formulation of complete remedial action alternatives
Analysis, selection, and description of a complete remedial action
alternative
Conceptual design elements, including identification of pre-design testing
such as pilot studies
Monitoring requirements and performance metrics
Implementation schedule
The following Site conditions significantly limit the effectiveness of a number of
possible technologies.
The area that may require groundwater remediation is between the toe of
the basin dam and the compliance boundary to the north.
The COIs that may potentially need to be addressed are predominantly
found in the downgradient bedrock formations.
Groundwater flow is primarily through the upper fractured bedrock unit
and the highly heterogeneous bedrock transition zone.
The formations in question appear to be significantly heterogeneous and
appear to create anisotropic flow conditions.
The preliminary screening of potential groundwater corrective action follows:
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Source control by capping in place or excavation, and monitored natural
attenuation, will be vital components to the CAP.
Groundwater migration barriers. The lateral extent potentially required,
along with the depth and heterogenitity of the transition zone and
bedrock, may limit the feasibility of this technology.
Insitu chemical immobilization. This technology has not been
demonstrated to be effective for the primary COI, boron. It may be
applicable for other COIs.
Permeable reactive barrier. Similar to in-situ chemical immobilization,
permeable reactive barrier technology has not been demonstrated to be
effective for boron.
Groundwater extraction. Given Site conditions, preliminary screening of
potentially applicable technologies indicates that some form of
groundwater extraction could potentially be a viable choice as a key
element of groundwater corrective action in combination with source
control and MNA. However, further analysis is required and will be
addressed in the updated CAP.
Potentially viable options will be further evaluated in the CAP with updated fate
and transport and geochemical modeling.
Summary 15.4.2
This preliminary evaluation of corrective action alternatives is intended to
provide insight into the revised CAP preparation process, as outlined in 2L. It is
based on data currently available and on the current understanding of regulatory
requirements for the site. It addresses potentially applicable technologies and
remedial alternatives.
Potential approaches are based on the currently available information about site
geology/hydrogeology and COIs. In general, three hydrogeologic units or zones
of groundwater flow can be described for the site: shallow/surficial zone,
transition zone, and bedrock flow zone. The site COIs include a list of common
coal ash related metals such as boron and manganese.
If required, the potentially applicable technologies to supplement source control
and MNA include several groundwater extraction technologies such as
conventional vertical wells, along with angle-drilled and horizontal wells. All of
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these extraction technologies could also be augmented with fracturing of the
bedrock formation. Migration barriers, in-situ chemical immobilization, and
permeable reactive barriers are also identified as potentially applicable remedial
action alternatives. In the event that extracted groundwater may require
treatment prior to discharge, several water treatment technologies for the
relevant COIs would be evaluated, including pH adjustment, metals
precipitation, ion exchange, permeable membranes, and adsorption technologies.
The CAP will further evaluate basin closure options to reduce the potential
impacts to human health or the environment; short- and long-term effectiveness,
implementability, and potential for attenuation of contaminants; time and cost to
achieve restoration; public and economic benefits; and compliance with
applicable laws and regulations.
The CAP evaluation process will be used to determine which approach, or
combination of approaches, will be most effective. Modeling will also be used to
evaluate the various options prior to selection.
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2017 Comprehensive Site Assessment Update October 2017
Belews Creek Steam Station SynTerra
FIGURES
2017 Comprehensive Site Assessment Update October 2017
Belews Creek Steam Station SynTerra
TABLES