HomeMy WebLinkAbout1 MSS CAP Part 2_Report_FINALF)R
Corrective Action Plan Part 2
Marshall Steam Station Ash Basin
Site Location:
NPDES Permit No.
Permittee and Current
Property Owner:
Consultant Information:
Report Date:
Marshall Steam Station
8320 NC Highway 150 E
Terrell, NC 28682
NC0004987
Duke Energy Carolinas, LLC
526 South Church St
Charlotte, NC 28202
704.382.3853
HDR Engineering, Inc. of the Carolinas
440 South Church St, Suite 900
Charlotte, NC 28202
704.338.6700
March 3, 2016
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Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
Contents
Acknowledgements
ExecutiveSummary ................................................................................................................................
1 Introduction....................................................................................................................................
1.1
Regulatory Background.......................................................................................................
1.2
Report Organization............................................................................................................
2 Summary
of Previous and Current Studies...................................................................................
2.1
Comprehensive Site Assessment.......................................................................................
2.1.1 Identification of COls..............................................................................................
2.1.2 Soil Delineation......................................................................................................
2.1.3 Groundwater Delineation.......................................................................................
2.2
Corrective Action Plan Part 1..............................................................................................
2.2.1 Proposed Provisional Background Concentrations for Soil and Groundwater ......
2.2.2 COI Occurrence and Distribution...........................................................................
2.3
Round 2 Sampling...............................................................................................................
2.3.1 Groundwater...........................................................................................................
2.3.2 Round 1 and Round 2 Source Area and Groundwater Data Comparison .............
2.3.3 Surface Water and Area of Wetness......................................................................
2.4
Round 3 and Round 4 Background Well Sampling.............................................................
3 Site Conceptual Model..................................................................................................................
3.1
Identification of Potential Contaminants..............................................................................
3.2
Identification and Characterization of Source Contaminants ..............................................
3.3
Delineation of Potential Migration Pathways through Environmental Media ......................
3.3.1 Soil..........................................................................................................................
3.3.2 Groundwater...........................................................................................................
3.3.3 Surface Water and Sediment.................................................................................
3.4
Establishment of Background Areas...................................................................................
3.5
Environmental Receptor Identification and Discussion.......................................................
3.6
Determination of System Boundaries..................................................................................
3.7
Site Geochemistry and Influence on COls..........................................................................
4 Modeling........................................................................................................................................
4.1
Groundwater Model Refinement.........................................................................................
4.1.1 Flow Model Refinements........................................................................................
4.1.2 Contaminant Fate and Transport Model Refinements ...........................................
4.1.3 Summary of Modeled Results................................................................................
4.1.4 Model Assumptions and Limitations.......................................................................
4.1.5 Modeled Scenario Results.....................................................................................
4.2
Surface Water Model Refinement.......................................................................................
4.2.1 Methodology...........................................................................................................
4.2.2 Results...................................................................................................................
4.3
Geochemical Modeling........................................................................................................
4.3.1 Objective................................................................................................................
4.3.2 Methodology...........................................................................................................
4.3.3 Assumptions...........................................................................................................
4.3.4 Geochemical Model Results..................................................................................
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Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
4.4 Refined Site Conceptual Model............................................................................................... 34
5
Risk Assessment...............................................................................................................................
35
5.1
Step 1: Conceptual Site Model................................................................................................
35
5.2
Step 2: Risk -Based Screening................................................................................................
36
5.3
Step 3: Human Health Risk Assessment................................................................................37
5.4
Step 4: Ecological Risk Assessment.......................................................................................
38
6
Alternative Methods for Achieving Restoration.................................................................................
40
6.1
Corrective Action Decision Process........................................................................................
40
6.1.1 Evaluation Criteria......................................................................................................40
6.1.2 COIs Requiring Corrective Action..............................................................................
41
6.1.3 Potential Exposure Routes and Receptors................................................................
41
6.2
Alternative Evaluation Criteria.................................................................................................41
6.2.1 Effectiveness..............................................................................................................
42
6.2.2 Implementability/Feasibility........................................................................................
42
6.2.3 Environmental Sustainability......................................................................................43
6.2.4 Cost............................................................................................................................
44
6.2.5 Stakeholder Input.......................................................................................................
44
6.3
Remedial Alternatives to Achieve Regulatory Standards.......................................................
44
6.3.1 Groundwater Remediation Alternatives.....................................................................
44
6.3.2 Monitored Natural Attenuation Applicability to Site....................................................45
6.3.3 Site -Specific Alternatives Analysis.............................................................................
46
6.3.4 Site -Specific Recommended Approach.....................................................................
49
7
Selected Corrective Action(s)............................................................................................................
51
7.1
Selected Remedial Alternative for Corrective Action..............................................................
51
7.2
Conceptual Design..................................................................................................................
51
7.2.1 Source Control — Cap-in-Place..................................................................................
51
7.2.2 MNA............................................................................................................................
52
8
Recommended Interim Activities.......................................................................................................
53
8.1
Additional Monitoring Well Installation....................................................................................
53
8.2
Additional Groundwater Sampling and Analyses....................................................................
53
9
Interim
and Effectiveness Monitoring Plans......................................................................................54
9.1
Interim Monitoring Plan...........................................................................................................
54
9.1.1 Data Quality Objectives..............................................................................................
54
9.1.2 Sampling Requirements.............................................................................................55
9.1.3 Reporting....................................................................................................................55
9.2
Effectiveness Monitoring Plan.................................................................................................56
9.2.1 Data Quality Objectives..............................................................................................
56
9.2.2 Sampling Requirements.............................................................................................56
9.2.3 Reporting....................................................................................................................57
9.3
Sampling and Analysis............................................................................................................
57
9.3.1 Monitoring Well Measurements and Inspection.........................................................
57
9.3.2 Surface Water Measurements...................................................................................
58
9.3.3 Sample Collection......................................................................................................
58
9.3.4 Quality Assurance/Quality Control.............................................................................
60
10
Implementation Cost and Schedule..................................................................................................
61
10.1
Implementation Cost...............................................................................................................
61
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Marshall Steam Station Ash Basin
10.2 Implementation Schedule........................................................................................................ 62
11 References
Tables
63
2-1 Summary of Horizontal Hydraulic Gradient Calculations
2-2 Exceptions to Vertical Hydraulic Gradients*
2-3 Comparison of COI Sample Results using 0.45 pm and 0.1 pm Filters
2-4 Ash Porewater Analytical Results — Round 1 and Round 2
2-5 Ash Basin Water Analytical Results — Round 1 and Round 2
2-6 Background Groundwater Analytical Results — Rounds 1 through 4
2-7 Groundwater Analytical Results Upgradient of Source Areas — Round 1 and Round 2
2-8 Groundwater Analytical Results Beneath and Adjacent to Ash Basin — Round 1 and Round 2
2-9 Groundwater Analytical Results Beneath the Dry Ash Landfill (Phase II) — Round 1 and Round 2
2-10 Groundwater Analytical Results Downgradient and East of Ash Basin and Dry Ash Landfill (Phase
1) — Round 1 and Round 2
2-11 Groundwater Analytical Results Downgradient and Southeast of Ash Basin — Round 1 and Round
2
2-12 Constituents of Interest Evaluation
2-13 Surface Water Sample Analytical Results — Round 1 and Round 2
2-14 Areas of Wetness Sampling Analytical Results — Round 1 and Round 2
4-1 Summary of Modeled COI Results at the Compliance Boundary*
4-2 Lake Norman Calculated Surface Water Concentrations
9-1 Interim Monitoring Plan Sample Locations
9-2 Sampling Parameters and Analytical Method
10-1 Estimated Capital and Annual Costs for Corrective Action - MNA*
* Table is presented within the text of this CAP Part 2 Report.
Figures
2-1 Site Sampling Locations
2-2 Water Table Surface Map — Shallow Wells (S)
2-3 Potentiometric Surface Map — Deep Wells (D)
2-4 Potentiometric Surface Map — Bedrock Wells (BR)
2-5 Areas of Exceedances
3-1 Site Conceptual Model — 3D Representation
3-2 Site Conceptual Model — Cross Sectional (4 Sheets)
3-3 Receptor Map
8-1 Additional Assessment Wells
Appendices
A CSA Addendum
B Groundwater Flow and Transport Model
C Addendum to Soil Sorption Evaluation
D Surface Water Mixing Model Approach
C Geochemical Modeling Report
D Baseline Human Health and Ecological Risk Assessment
E Evaluation of Potential Groundwater Remedial Alternatives
F Monitored Natural Attenuation Technical Memorandum
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
Acronyms and Abbreviations
tag/L
micrograms per liter
2B Standard
North Carolina surface water standards as specified in T15 NCAC 02B
.0211 and .0216 (amended effective January 2015)
2L Standard
North Carolina groundwater standards as specified in T15A NCAC 02L
3-D
three-dimensional
AOW
area of wetness
ASTM
ASTM International
BERA
Baseline Ecological Risk Assessment
BG
background
BR
bedrock
CAMA
North Carolina Coal Ash Management Act of 2014
CAMC
North Carolina Coal Ash Management Commission
CAP
Corrective Action Plan
CCR
coal combustion residuals
COI
constituent of interest
COPC
contaminant of potential concern
CSA
Comprehensive Site Assessment
D
deep
DO
dissolved oxygen
DQO
data quality objectives
Duke Energy
Duke Energy Carolinas, LLC
DWR
NCDEQ Division of Water Resources
Eh
oxidation-reduction potential (see also ORP)
EPC
exposure point concentration
EPRI
Electric Power Research Institute
FGD
flue gas desulfurization
ft bgs
feet below ground surface
ft/ft
feet / foot
HAO
hydrous aluminum oxide
HFO
hydrous ferric oxide
HQ
hazard quotient
HSL
health screening level
IMAC
interim maximum allowable concentration
Kd
sorption coefficient
mg/kg
milligrams per kilogram
MNA
monitored natural attenuation
MW
monitoring well
MSS
Marshall Steam Station
NC PSRGs
North Carolina Preliminary Soil Remediation Goals
NCAC
North Carolina Administrative Code
iv
Corrective Action Plan Part 2
Marshall Steam Station Ash Basin
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
NPDES
National Pollutant Discharge Elimination System
NTU
nephelometric turbidity units
ORP
oxidation-reduction potential
POG
protection of groundwater
PPBC
proposed provisional background concentration
PRB
permeable reactive barrier
PV
photovoltaic
RBC
risk -based concentrations
SCM
site conceptual model
TDS
total dissolved solids
UNCC
University of North Carolina at Charlotte
USEPA
U.S. Environmental Protection Agency
USGS
U.S. Geological Survey
Work Plan
Groundwater Assessment Work Plan
Corrective Action Plan Part 2
Marshall Steam Station Ash Basin
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Corrective Action Plan Part 2 F)�
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Acknowledgements
HDR would like to express its appreciation to Duke Energy for its comments and interim report
reviews, and to the parties listed below for their assistance with data analysis, report
preparation, quality reviews, and overall development of this corrective action plan.
The University of North Carolina at Charlotte — Groundwater modeling and soil sorption
analysis
Electric Power Research Institute — Groundwater flow and transport model third -party peer
review
Geochemical, LLC — Monitored natural attenuation evaluation and soil sorption analysis
CH2M Hill, Inc. — Remedial alternative analysis
Leggette, Brashears & Graham, Inc — Groundwater modeling
Haley & Aldrich, Inc. — Risk assessment third -party peer review
Corrective Action Plan Part 2
Marshall Steam Station Ash Basin
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Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
Executive Summary
The North Carolina Coal Ash Management Act of 2014 (CAMA) directs owners of coal
combustion residuals (CCR) surface impoundments in North Carolina to conduct groundwater
monitoring, assessment, and remedial activities, if necessary. A Groundwater Assessment Work
Plan (Work Plan) for the Marshall Steam Station (MSS) was submitted to the North Carolina
Department of Environment and Natural Resources (NCDENR) on September 24, 2014, and
was subsequently revised on December 30, 2014. The revised Work Plan was conditionally
approved by NCDENR on March 12, 2015. A Comprehensive Site Assessment (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. The MSS CSA Report was submitted to
NCDENR on September 8, 2015 (HDR 2015a).
Subsequent to submittal of the CSA Report, CAMA requires submittal of a Corrective Action
Plan (CAP) for each regulated facility no later than 180 days after submittal of the CSA Report.
Duke Energy Carolinas, LLC (Duke Energy) and the North Carolina Department of
Environmental Quality (NCDEQ)' agreed to a two-part CAP submittal, with Part 1 being
submitted within 90 days of submittal of the CSA Report and Part 2 being submitted no later
than 180 days after submittal of the CSA Report. The MSS CAP Part 1 Report was submitted to
NCDEQ on December 7, 2015 (HDR 2015b).
On December 31, 2015, NCDEQ released draft proposed risk classifications for Duke Energy's
coal ash impoundments in North Carolina. The proposed risk classification for the MSS ash
basin was low -to -intermediate. Risk classifications were based upon potential risk to public
health and the environment. A public meeting regarding the proposed risk classification for the
MSS impoundments is scheduled for March 29, 2016. NCDEQ will release the final risk
classifications, subject to approval by the North Carolina Coal Ash Management Commission
(CAMC), after review of public comments.
Duke Energy owns and operates MSS, located in Catawba County near the town of Terrell,
North Carolina. MSS began operations in 1965 as a coal-fired generating station and currently
operates four coal-fired units. CCR consisting of bottom and fly ash material from MSS has
been disposed in the station's ash basin, located north of the station adjacent to Lake Norman,
since the basin was constructed. Dry ash has been disposed in other areas at the site including
the dry ash landfill units (Phases I and II) and Industrial Landfill No. 1. Flue gas desulfurization
(FGD) residue (i.e., gypsum) and fly ash were disposed in the FGD residue landfill, which was
placed in intermediate closure in October 2015. Fly ash utilized as structural fill was placed in
the photovoltaic (PV) structural fill and was used as structural fill beneath portions of the
Industrial Landfill No. 1. Discharge from the ash basin is permitted by the NCDEQ Division of
Water Resources (DWR) under the National Pollutant Discharge Elimination System (NPDES)
Permit NC0004987.
Prior to September 18, 2015, the NCDEQ was referred to as the NCDENR. Both naming conventions are used in
this report, as appropriate.
1
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
Groundwater at the MSS site generally flows from the north and northwest extents of the
property boundary to the south and southeast beneath the source areas toward Lake Norman,
which serves as the hydrologic boundary downgradient of the CCR source areas.
Based on evaluation of data presented in the CSA Report, groundwater concentrations of
constituents of interest (COIs)Z attributable to source areas at the MSS site were identified
beneath the ash basin, beneath the dry ash landfill units, and downgradient of the ash basin.
COI transport in groundwater is consistent with the direction of groundwater flow. COls in
groundwater attributable to ash handling at the MSS site are: antimony, arsenic, barium,
beryllium, boron, chromium3, cobalt, iron, manganese, selenium, sulfate, thallium, total
dissolved solids (TDS), and vanadium. Note that antimony, barium, chromium, cobalt,
hexavalent chromium, iron, manganese, thallium, and vanadium were also detected above their
groundwater quality standard or criteria in site background groundwater. Further sampling and
analyses are necessary to determine if COI exceedances are the result of source -related
impacts or naturally occurring conditions (as discussed in Section 2).
Groundwater fate and transport modeling was performed for two closure scenarios for the MSS
ash basin during CAP Part 2: An Existing Conditions scenario with ash sources left in place and
a Cap -in -Place scenario, which simulates the effects of covering the ash basin with an
engineered cap at the beginning of the predictive simulation. The refined groundwater model
predicts that certain COls will exceed regulatory standards or criteria at the Compliance
Boundary4 in the Cap -in -Place closure scenario, as discussed in Section 4.1.5; however, based
on results of the groundwater to surface water interaction modeling, no surface water quality
standards or criteria are exceeded at the edge of the mixing zones in Lake Norman.
A human health and ecological risk assessment was conducted as part of this CAP. Evaluation
of potential impacts to humans indicates that risk estimates for several COPCs are above risk
targets for the recreational fisher and subsistence fisher from ingestion of fish caught near the
site. Additional data regarding site -specific conditions, delineation of source -related and
background COls applicable to the risk assessment, and evaluation of the exposure parameters
and fish ingestion models used in the risk assessment are needed to qualify these results.
Evaluation of potential impacts to ecological receptors indicates that risk estimates for several
COPCs are above risk targets for some water -dependent birds, if and where these species are
present at the MSS site. Additional data and further refined assessment are needed to address
uncertainties associated with the evaluation of these scenarios including the occurrence of
these ecological receptors in the areas adjacent to the ash basin, delineation of source -related
2 If a constituent concentration exceeded the North Carolina Groundwater Quality Standards as specified in Title 15A
NCAC .0202L (2L Standards), Interim Maximum Allowable Concentration (IMAC), North Carolina Preliminary Soil
Remediation Goals for Protection of Groundwater (NC PSRGs for POG), North Carolina Department of Health and
Human Services Health Screening Level (NCDHHS HSL), North Carolina Surface Water Quality Standards as
specified in T15 NCAC 02B .0211 and .0216 (amended effective January 2015) (213 Standards), or U.S.
Environmental Protection Agency National Recommended Water Quality Criteria, it has been designated as a
"constituent of interest".
3 Unless otherwise noted, references to chromium in this document indicate total chromium.
4 Per 15A NCAC 02L .0102, "Compliance Boundary" means a boundary around a disposal system at and beyond
which groundwater quality standards may not be exceeded and only applies to facilities which have received a
permit issued under the authority of G.S. 143-215.1 or G.S. 130A.
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
and background Cols applicable to the risk assessment, and refinement of the exposure and
toxicity assumptions used in the ecological risk characterization.
Based on evaluation of data collected to date, Duke Energy is proposing to utilize cap -in -place
as a source control measure at the MSS ash basin. The cap -in -place option would consist of
constructing an engineered cap system over the ash areas. The final closure option selected will
be modified as required based on the final risk classification proposed by NCDEQ and approved
by the North Carolina CAMC.
An evaluation of site conditions, constituents, and a review of alternative methods for restoring
groundwater quality found that, in conjunction with the planned source control, monitored
natural attenuation (MNA) is recommended as a supplemental corrective action for groundwater
impacts beneath the site. In addition, further investigation should be conducted to evalaute the
effectiveness of a groundwater cutoff wall to intercept groundwater flowing from the ash basin to
the unnamed tributary east of the basin.
An Interim Monitoring Plan has been developed to provide baseline seasonal groundwater data
for the MSS site and will be implemented with sampling activities planned for the first two
quarters of 2016. Interim monitoring results will be used to evaluate compliance and may be
used, as needed, to refine the groundwater contaminant fate and transport, groundwater to
surface water interaction, and geochemical models. Although Duke Energy acknowledges that
groundwater quality may be influenced by basin closure activities, an Effectiveness Monitoring
Plan will be implemented prior to completion of closure to monitor these potential affects and
establish a baseline for MNA effectiveness monitoring. The monitoring results will also be used
to confirm that attenuation of COls is continuing to occur and remains an effective corrective
action for groundwater at the MSS site. If MNA is deemed insufficient for restoration of
groundwater quality, other alternatives discussed in Section 6.3.3 should be evaluated and, if
warranted, implemented to augment the MNA processes. The performance of these corrective
actions will continue to be monitored and evaluated to determine if modifications to the
measures are warranted.
Per CAMA §130A-309.209.(b)(1), "The Groundwater Corrective Action Plan shall provide for the
restoration of groundwater in conformance with the requirements of Subchapter L of Chapter 2
of Title 15A of the North Carolina Administrative Code." This CAP meets the requirements of
15A NCAC 02L .0106 and the requirements of the referenced section of CAMA.
Corrective Action Plan Part 2
Marshall Steam Station Ash Basin
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Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
1 Introduction
Duke Energy Carolinas, LLC (Duke Energy) owns and operates the Marshall Steam Station
(MSS), located in Catawba County near the town of Terrell, North Carolina. MSS began
operations in 1965 as a coal-fired generating station and currently operates four coal-fired units.
Coal combustion residual (CCR) consisting of bottom and fly ash material from MSS has been
disposed in the station's ash basin, located north of the station adjacent to Lake Norman, since
construction of the ash basin. Dry ash has been disposed in other areas at the site including the
dry ash landfill units (Phases I and II) and Industrial Landfill No. 1. Flue gas desulfurization
(FGD) residue (i.e., gypsum) and fly ash were disposed in the FGD residue landfill, which was
placed in intermediate closure in October 2015. Fly ash was used as structural fill in the
photovoltaic (PV) structural fill and beneath portions of the Industrial Landfill No. 1. Discharge
from the ash basin is permitted by the North Carolina Department of Environmental Quality
(NCDEQ)5 Division of Water Resources (DWR) under the National Pollutant Discharge
Elimination System (NPDES) Permit NC0004987.
1.1 Regulatory Background
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. A Groundwater Assessment Work Plan (Work Plan) for MSS was
submitted to North Carolina Department of Environment and Natural Resources (NCDENR) on
September 24, 2014, followed by a revised Work Plan on December 30, 2014. The revised
Work Plan was conditionally approved by NCDENR on March 12, 2015. A Comprehensive Site
Assessment (CSA) was performed to collect information necessary to evaluate 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. The MSS CSA Report was
submitted to NCDENR on September 8, 2015 (HDR 2015a).
CAMA Section §130A-309.209(b) requires implementation of corrective action for the
restoration of groundwater quality in accordance with the North Carolina Administrative Code
(T15A NCAC 02L) and requires the submittal of a Corrective Action Plan (CAP) for each
regulated facility no later than 180 days after submittal of the CSA. Duke Energy and NCDEQ
mutually agreed to a two-part CAP submittal, with Part 1 being submitted within 90 days of
submittal of the CSA Report and Part 2 being submitted no later than 180 days after submittal of
the CSA Report.
The MSS CAP Part 1 Report (HDR 2015b) was submitted to NCDEQ on December 7, 2015 and
consisted of the following:
• background information
• brief summary of the CSA findings
• brief description of the site geology and hydrogeology
5 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.
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
• summary of the previously completed receptor survey
• summary of constituent of interest (COI) exceedances and distribution
• development of proposed provisional background concentrations (PPBCs) for soil and
groundwater
• detailed description of the site conceptual model (SCM)
• results of the groundwater flow and fate and transport model
• results of the groundwater to surface water interaction model
The purpose of this CAP Part 2 is to provide the following:
• a description of exceedances of groundwater quality standards, surface water quality
standards, and sample results greater than the Interim Maximum Allowable
Concentrations (IMAC) and North Carolina Department of Health and Human Services
(NCDHHS) health screening levels (HSL)
• present Round 3 and 4 background sampling results
• a refined SCM
• refined groundwater flow and fate and transport model results
• refined groundwater to surface water model results
• site geochemical model results
• findings of the risk assessment
• evaluation of methods for achieving groundwater quality restoration
• conceptual plan(s) for recommended proposed corrective action(s)
• a schedule for implementation of the proposed corrective action(s)
• a plan for monitoring and reporting of the effectiveness of the proposed corrective
action(s)
The information provided in the combined CAP Part 1 and CAP Part 2 meets the requirements
of regulation 15A NCAC 02L .0106 (f) for corrective action.
Regulation 15A NCAC 02L .0106 (f)(4) requires that the secondary sources, which could be
potential continuing sources of possible pollutants to groundwater, be addressed in the CAP. At
the MSS site, the soil located below the ash basin, dry ash landfill units and PV structural fill
could be considered as potential secondary sources. Information collected to date indicates that
the thickness of soil impacted by ash is generally limited to the depth near the ash -soil interface.
This proposed corrective action plan considers cap -in -place as the source control measure for
the ash basin. An engineered cap will minimize infiltration through the covered area reducing
possible impacts from potentially impacted soil. Therefore, remediation of soils is not discussed
in this report.
On December 31, 2015, NCDEQ released draft proposed risk classifications for Duke Energy's
coal ash impoundments in North Carolina. The proposed risk classification issued for the MSS
ash basin was low -to -intermediate. The risk classification was based upon potential risk to
public health and the environment. A public meeting regarding the proposed risk classification
for the MSS ash basin is scheduled for March 29, 2016. According to the CAMA, NCDEQ will
submit its final risk classifications for review and approval by the North Carolina Coal Ash
Management Commission (CAMC) after review of public comments.
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
1.2 Report Organization
The information identified above has been organized in this CAP Part 2 report as follows:
• Section 1 provides an introduction to the MSS site and the intent of corrective action
under CAMA.
• Section 2 provides a summary of the CSA and CAP Part 1 reports; a comparison of
Round 1 and Round 2 groundwater, surface water, and area of wetness (AOW)
sampling results; and a summary of Round 3 and Round 4 background well sampling
results.
• Section 3 discusses the SCM and site geochemical controls on contaminant mobility.
• Section 4 discusses purpose, methodologies, and results of refined groundwater,
groundwater to surface water interaction, and geochemical modeling. Refinement of the
SCM following evaluation of model results is also discussed in this section.
• Section 5 provides a summary of the human health and ecological risk assessments.
• Section 6 presents an evaluation of remedial alternatives to achieve groundwater
restoration.
• Section 7 provides a concept -level discussion and plans for recommended corrective
action(s).
• Section 8 discusses recommended interim activities to be initiated in 2016.
• Section 9 provides a plan for interim and effectiveness groundwater monitoring.
• Section 10 provides a schedule and cost opinion for CAP implementation and post -CAP
monitoring.
Applicable tables, figures, and appendices with supporting documents are included with this
report.
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
2 Summary of Previous and Current Studies
This section presents a summary of previous and current studies including the following:
• Summary of the CSA.
• Summary of the CAP Part 1.
• Presentation of Round 2 groundwater, surface water, and AOW sampling results
including comparison to Round 1 sampling results.
• Presentation of Round 3 and 4 background well sampling results.
Round 1 sampling data were previously provided in the CSA Report. Subsequent sampling
rounds occurred after the CSA Report submittal and are presented in this CAP Part 2 Report.
2.1 Comprehensive Site Assessment
The purpose of the MSS CSA was to collect information necessary to characterize the extent of
impacts resulting from historical production and storage of coal ash, evaluate the chemical and
physical characteristics of the contaminants, investigate the geology and hydrogeology of the
site including factors relating to contaminant transport, and examine risk to potential receptors
and exposure pathways. The following assessment activities were performed as part of the
CSA.
• Completion of soil borings and installation of groundwater monitoring wells to facilitate
collection and analysis of chemical, physical, and hydrogeological parameters of
subsurface materials encountered within and beyond the waste and Compliance
Boundary(s)s.
• Evaluation of laboratory analytical data to support the SCM.
• Update of the receptor survey previously completed in September 2014 (updated
November 2014) (HDR 2014a, 2014b).
• Completion of a screening -level risk assessment.
Note that subsequent to submittal of the CSA Report, additional evaluation of Round 1 sampling
results has been conducted. Responses to NCDEQ comments and additional information in
response to the exceptions identified in the CSA Report are provided in Appendix A.
2.1.1 Identification of COIs
If a constituent concentration exceeded the North Carolina Groundwater Quality Standards, as
specified in T15A NCAC .0202L (2L Standards), IMACs', NCDHHS HSL (hexavalent chromium
only), North Carolina Preliminary Soil Remediation Goals (NC PSRGs) for Protection of
6 Per 15A NCAC 02L .0102, "Compliance Boundary" means a boundary around a disposal system at and beyond
which groundwater quality standards may not be exceeded and only applies to facilities which have received a
permit issued under the authority of G.S. 143-215.1 or G.S. 130A.
' Appendix #1 of 15A NCAC Subchapter 02L Classifications and Water Quality Standards Applicable to The
Groundwaters of North Carolina, lists Interim Maximum Allowable Concentrations (IMACs). The IMACs were issued
in 2010 and 2011; however, NCDENR has not established a 2L Standard for these constituents as described in 15A
NCAC 02L.0202(c). For this reason, IMACs noted in this report are for reference only.
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
Groundwater (POG), North Carolina Surface Water Quality Standards as specified in 15 NCAC
02B .0211 and .0216 (amended effective January 2015) for Class WS-V waters (213 Standards),
or U.S. Environmental Protection Agency (USEPA) National Water Quality Criteria (USEPA
Criteria), it was designated as a COI. The following constituents were reported as COls in the
CSA Report:
• Soil: arsenic, barium, cobalt, iron, manganese, nickel, selenium, and vanadium
• Groundwater: antimony, arsenic, barium, beryllium, boron, chromium$, cobalt, iron,
manganese, selenium, sulfate, thallium, total dissolved solids (TDS), and vanadium.
• Surface water: cobalt, iron, manganese, sulfate, and TDS.
In addition to COI identification, delineation of COls in site media was also conducted during the
CSA. Soil and groundwater delineation is further discussed below.
2.1.2 Soil Delineation
The horizontal extent of soil impacts identified during the CSA was limited to the area beneath
the ash basin and one location east and downgradient of the dry ash landfill (Phase 1). Where
soil impacts were identified beneath the ash basin, the vertical extent of contamination beneath
the ash/soil interface was generally limited to the uppermost soil sample collected beneath the
ash.
2.1.3 Groundwater Delineation
The approximate horizontal extent of groundwater impacts identified during the CSA was limited
to within the ash basin Compliance Boundary, specifically beneath the ash basin and dry ash
landfill (Phase II), east and downgradient of the ash basin and dry ash landfill (Phase 1), and
southeast and downgradient of the ash basin, within the ash basin Compliance Boundary. The
approximate vertical extent of groundwater impacts is generally limited to the shallow and deep
flow layers, and vertical migration of COls is impeded by the underlying bedrock.
Groundwater impacts at the MSS site attributable to ash handling and storage was delineated
during the CSA activities with the following areas requiring refinement:
• Horizontal and vertical extent of groundwater impacts downgradient and east of the ash
basin and dry ash landfill (Phase 1).
Based on the exceptions noted above and subsequent discussions with NCDEQ, a total of four
additional monitoring wells are scheduled to be installed in this area of the site in March 2016 to
further delineate groundwater impacts. In addition, one soil boring will be advanced east and
downgradient of the dry ash landfill (Phase 1) to confirm the soil impacts identified during the
CSA. Results of the additional monitoring well installation and groundwater sampling and soil
sampling will be submitted under separate cover.
8 Unless otherwise noted, references to chromium in this document should be assumed to indicate total chromium.
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
2.2 Corrective Action Plan Part 1
The purpose of CAP Part 1 was to summarize CSA findings, evaluate background conditions by
calculating PPBCs, evaluate exceedances per sample medium with regard to PPBCs, refine the
SCM, and present the results of the groundwater flow and contaminant fate and transport
model, and groundwater to surface water interaction model.
2.2.1 Proposed Provisional Background Concentrations for Soil and
Groundwater
HDR used background soil and groundwater concentrations to determine site -specific
background concentrations for each COI. Because COls can be both naturally occurring and
related to the source area, the selection of borings and monitoring wells used to establish
background concentrations is important in determining whether releases have occurred from the
source areas and to define the concentration of source -related compounds exceeding the
background concentration for corrective action. A detailed analysis of background soil and
groundwater PPBCs was provided in the CAP Part 1 Report. Further refinement of the PPBCs
is anticipated following evaluation of data from Round 3 and Round 4 sampling events
(completed in 2015), additional background monitoring planned in 2016, and the interim and
effectiveness sampling planned in 2016 (Section 8 and 9).
2.2.2 COI Occurrence and Distribution
Several COls exceeded both their NC PSRGs for POG and PPBCs in soil samples collected
during the CSA and are listed below with respect to each area of the site.
Beneath the Ash Basin: arsenic, iron, manganese, and vanadium.
Beneath the Dry Ash Landfill (Phase II): arsenic, manganese, and vanadium.
Beneath the PV Structural Fill: arsenic, manganese, and selenium.
Outside Source Area Waste Boundaries: arsenic, iron, manganese, selenium, and vanadium.
The vertical extent of soil impacts is generally limited to the shallow soil samples collected
beneath the source areas.
As a result of constituents leaching from the ash basin and dry ash landfill units (Phase I and II),
and geochemical processes taking place in groundwater and soil beneath the site, several COls
in groundwater exceeded their PPBCs and/or 2L Standard, IMAC or NCDHHS HSL (hexavalent
chromium only), and are listed below with respect to each area of the site.
Beneath the Ash Basin: antimony, boron, chloride, cobalt, iron, manganese, TDS, and
vanadium.
Beneath the Dry Ash Landfill (Phase II): barium, boron, chromium, cobalt, iron, manganese,
selenium, sulfate, TDS, and vanadium.
Downgradient and East of the Ash Basin and Dry Ash Landfill (Phase 1): beryllium, boron,
chloride, chromium, hexavalent chromium, cobalt, manganese, thallium, TDS, and vanadium.
10
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
Downgradient of the Ash Basin Dam: arsenic, boron, cobalt, hexavalent chromium, iron,
manganese, thallium, TDS, and vanadium.
The areas of 2L Standard, IMAC, or NCDHHS HSL exceedances beneath and downgradient of
the source areas indicate that physical and geochemical processes beneath the site inhibit the
lateral migration of COls. Vertical migration of COls was observed in select well clusters
(shallow, deep, and bedrock) and is likely influenced by infiltration of precipitation and/or ash
basin water, where applicable, through the shallow and deep flow layers into underlying
fractured bedrock. Groundwater from the shallow and deep flow layers at the site discharges to
Lake Norman and the unnamed tributary east of the ash basin and dry ash landfill (Phase 1), as
described in the SCM section of this report (Section 3). The extent of impacted groundwater is
being refined through the installation of additional monitoring wells, as discussed in Section 2.1.
In the CAP Part 1, groundwater model results for several Cols showed concentrations to be
above applicable groundwater standards or criteria at the Compliance Boundary or Lake
Norman for both current conditions and future scenarios modeled. However, based on
groundwater to surface water interaction model results, all water quality standards are less than
applicable criteria at the edge of the mixing zones in the Lake Norman.
2.3 Round 2 Sampling
Round 2 groundwater, ash porewater, ash basin water, surface water, and AOW sampling
activities were completed between September 28 and October 7, 2015. Groundwater analytical
parameters and methods were consistent with those employed for Round 1, as detailed in CSA
Report Table 7-3. The following subsections provide a comparison of Round 1 to Round 2
groundwater flow and analytical results.
2.3.1 Groundwater
A total of 62 groundwater monitoring wells were sampled during the Round 2 event including, 12
compliance monitoring wells installed during the CSA, seven voluntary monitoring wells, and
one FGD residue landfill monitoring well. Samples were collected for total and dissolved
concentration analyses. Monitoring well locations are depicted on Figure 2-1.
2.3.1.1 Groundwater Water Levels
On September 28, 2015, monitoring wells were manually gauged from the top of the PVC
casing using an electronic water level indicator.
Groundwater elevations and contours for the shallow, deep, and bedrock flow layers are
depicted on Figures 2-2, 2-3, and 2-4, respectively. Groundwater elevations calculated during
the Round 2 water level gauging event were generally similar to or slightly higher than those
calculated from the Round 1 water level gauging data. The differences are likely attributable to
seasonal variations of the water table. Depth to water measurements were not collected from all
the monitoring wells gauged during the Round 1 sampling event and thus do not allow for
groundwater contours to be depicted for the extent included in the CSA Report.
11
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
2.3.1.2 Horizontal and Vertical Gradients
Horizontal hydraulic gradients were updated using Round 2 groundwater elevations for the
shallow, deep, and bedrock flow layers by calculating the difference in hydraulic heads over the
length of the flow path between two wells with similar well construction (e.g., both wells having
15-foot screens within the same water -bearing unit). Monitoring wells, groundwater elevations,
and length of flow paths utilized for horizontal hydraulic gradient calculations are detailed in
Table 2-1. The average horizontal hydraulic gradients for Round 2 compared to Round 1 are
provided below:
• Shallow flow layer: Round 2 - 0.017 feet/foot; Round 1 - 0.018 feet/foot
• Deep flow layer: Round 2 - 0.016 feet/foot; Round 1 - 0.017 feet/foot
• Bedrock flow layer: Round 2 - 0.010 feet/foot; Round 1 - 0.010 feet/foot
Horizontal hydraulic gradients were consistent with those documented in the CSA Report.
From the Round 2 data, vertical hydraulic gradients were calculated for 39 shallow and deep
well pairs and eight deep and bedrock well pairs by dividing the difference in groundwater
elevation in each well pair by the difference in elevation of well screen midpoints. In general, the
gradients showed potential vertical flow in the same direction in Rounds 1 and 2 with the
exceptions listed below in Table 2-2.
Table 2-2 Exceptions to Vertical Hydraulic Gradients
Round 1 Vertical
Round 2 Vertical
Shallow Well
Deep Well
Gradient (ft/ft)
Gradient (ft/ft)
GWA-1 S
GWA-1 D
-0.001
0.016
GWA-4S
GWA-4D
-0.005
0.967
MW-4
MW-4D
-0.011
0.400
Round 1 Vertical
Round 2 Vertical
Deep Well
Bedrock Well
Gradient (ft/ft)
Gradient (ft/ft)
MW-14D
MW-14BR
-0.233
0.057
2.3.1.3 Groundwater Sampling Procedures
Groundwater samples were collected using low -flow sampling techniques, as outlined in the
Low Flow Sampling Plan developed for the ash basin groundwater assessment program and
approved by NCDENR (CSA Report Appendix G). The samples were submitted to a laboratory
for analysis of total and dissolved inorganic parameters (USEPA Methods 200.7/200.8, 245.7,
and 218.7) and water quality parameters.
A 0.45-micron filter was used for collection of groundwater samples for dissolved concentration
analysis. During Round 2, additional sample volume was collected at select locations using a
0.1-micron filter for dissolved concentration analysis along major flow paths and at locations
with constituent concentrations that may be more affected by turbidity. The following monitoring
wells were sampled using the 0.1-micron filter:
12
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
AB-2D AB-41D AB-5BR
AB-8D AB-9BR AB-9D
AB-15BR AB-15D AB-17D
MW-8S
AB-5D
AB-6BR
AB-6D
AB-10D
AB-11 D
AB-12D
AB-18D
GWA-6D
MW-81D
Sample results from the 0.45-micron and 0.1-micron filters were generally similar. A comparison
of the analytical results from filtered samples is presented in Table 2-3.
2.3.2 Round 1 and Round 2 Source Area and Groundwater Data Comparison
Round 1 and Round 2 sample results are presented in Tables 2-4 through 2-8. Ash porewater
and groundwater concentrations in Round 2 remained similar to those observed in Round 1.
Variation from Round 1 to Round 2 cannot be further interpreted at this time as the data set
consists of only two comprehensive sampling events and, therefore, does not fully consider
seasonal fluctuations, or other temporal changes.
2.3.2.1 Source Area Results
Ash Porewater
The ash basin is a permitted wastewater treatment facility and ash porewater in the ash is
wastewater, not groundwater. Ash porewater is compared to 2L Standards or IMACs and
NCDHHS HSL for comparison purposes only.
Ash porewater samples were collected in Rounds 1 and 2 from locations within the sources
areas (Table 2-4). Ash porewater sample results from Round 2 were generally similar to Round
1 results except that zinc was identified as an additional COI in ash porewater (AB-5S) during
Round 2. Although the concentrations of zinc observed at AB-5S were similar in Rounds 1 and
2 (890 and 1,200 fag/L), this was the only location where zinc exceeded its 2L Standard.
Based on the Rounds 1 and 2 sampling results, COls in ash porewater are antimony, arsenic,
barium, beryllium, boron, cadmium, chloride, chromium, cobalt, hexavalent chromium, iron,
lead, manganese, nickel, pH, selenium, sulfate, thallium, TDS, vanadium, and zinc.
Ash Basin Water
The ash basin is a permitted wastewater treatment facility and water in the basin is wastewater,
not surface water. Ash basin water is compared to both 2B and 2L Standards or IMACs and
NCDHHS HSL for comparison purposes only, as ash basin water is a potential source of
groundwater and surface water impacts.
Ash basin water was collected from five locations: SW-1 through SW-5. Round 2 ash basin
water sample results were generally similar to or less than Round 1 results with the exceptions
noted below.
• SW-1 through SW-5 — aluminum was not analyzed during Round 1, and exceeded its 2B
Standard in each ash basin water sample during Round 2.
• SW-3 — manganese exceeded its 2B Standard during Round 2.
• SW-4 — arsenic exceeded its 2B Standard during Round 2.
13
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
• SW-4 and SW-5 — iron was not analyzed during Round 1, and exceeded its 2B Standard
in samples SW-4 and SW-5 during Round 2.
The following COls exceeded their regulatory standard or criteria in ash basin water samples
collected in Rounds 1 and 2: aluminum, arsenic, beryllium, cadmium, chloride, cobalt, copper,
iron, lead, manganese, mercury, nickel, selenium, sulfate, TDS, and zinc. Ash basin water
sample results from Round 1 and 2 are presented in Table 2-5.
2.3.2.2 Groundwater Results
Background Wells
In general, the constituent concentrations from the background monitoring wells exhibited
similar results when comparing data from the Round 1 and 2 sampling events. The following
constituents had concentrations exceeding their regulatory standard or criteria in groundwater
samples collected from background monitoring wells in Rounds 1 and 2: barium, chromium,
cobalt, hexavalent chromium, iron, lead, manganese, pH, thallium, and vanadium. This list of
COls is consistent with the COls reported in CAP Part 1. Note that hexavalent chromium was
only analyzed during Round 1 sampling from monitoring wells BG-1 S/D, MW-4, and MW-4D.
Background groundwater sample results from Round 1 and 2 are presented in Table 2-6.
Background monitoring wells will continue to be sampled and PPBCs recalculated as the data
set increases with additional sampling rounds.
Upgradient of Source Areas
Round 2 groundwater sample results for locations upgradient of the source areas were
generally similar to or less than Round 1 results with the following exceptions.
• GWA-3D — antimony and chromium did not exceed their 2L Standards during Round 2.
• GWA-3S — manganese did not exceed its 2L Standards during Round 2.
• GWA-4D — turbidity was less than 10 nephelometric turbidity units (NTU) during Round
2. Concentrations of iron and manganese decreased below their 2L Standards.
Antimony increased slightly above its 2L Standard.
• GWA-4S — turbidity was less than 10 NTU during Round 2. Although they still exceeded
their 2L Standard or IMAC, concentrations of cobalt, iron, manganese, and vanadium
decreased by approximately one order of magnitude. Chromium increased slightly above
its 2L Standard.
• GWA-5S — turbidity was less than 10 NTU during Round 2. Although they still exceeded
their 2L Standard or IMAC, concentrations of iron, manganese, and vanadium
decreased by approximately one order of magnitude. The concentration of cobalt
decreased below its IMAC.
• GWA-6D — antimony, iron, and manganese did not exceed their 2L Standards or IMAC
during Round 2. Vanadium decreased by approximately one order of magnitude but still
exceeded its IMAC.
• GWA-7D — iron and manganese did not exceed their 2L Standards during Round 2.
14
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
• GWA-7S — chromium and iron did not exceed their 2L Standards during Round 2.
Vanadium decreased by more than one order of magnitude but still exceeded its [MAC.
• GWA-8S — manganese did not exceed its 2L Standard during Round 2.
The following COls exceeded their regulatory standard or criteria in groundwater samples
collected from upgradient wells in both Rounds 1 and 2: antimony, chromium, cobalt, hexavalent
chromium, iron, manganese, pH, TDS, and vanadium. This list of COls is consistent with the
COls reported in CAP Part 1.
Groundwater sample results from monitoring wells located upgradient of the source areas for
Round 1 and 2 are presented in Table 2-7.
Beneath and Adjacent to the Ash Basin
Round 2 groundwater sample results for locations beneath and adjacent to the ash basin were
generally similar to or less than Round 1 results with the following exceptions.
• AB-17D — turbidity was less than 10 NTU during Round 2. Cobalt and iron did not
exceed their 2L Standard or IMAC during Round 2.
• AB-11 S -turbidity was less than 10 NTU during Round 2. Cobalt, iron, and vanadium did
not exceed their 2L Standard or IMAC during Round 2.
The following COls exceeded their regulatory standard or criteria in groundwater samples
collected from wells beneath and adjacent to the ash basin in both Rounds 1 and 2: antimony,
boron, chloride, cobalt, iron, manganese, pH, TDS, and vanadium. This list of COls is consistent
with the COls reported in CAP Part 1. Note that the only constituents that exceeded their
regulatory standard or criteria in wells located adjacent to the ash basin included cobalt, iron,
manganese, pH, and vanadium.
Groundwater sample results from monitoring wells located beneath and adjacent to the ash
basin for Round 1 and 2 are presented in Table 2-8
Beneath the Dry Ash Landfill (Phase 11)
Round 2 groundwater sample results for locations beneath the dry ash landfill (Phase II) were
generally similar to or less than Round 1 results with the following exceptions;
• AL-213R — antimony concentrations were similar in Round 1 and 2, but increased above
its IMAC in Round 2. Iron increased by more than one order of magnitude and exceeded
the 2L Standard in Round 2.
• AL-2D — selenium concentrations were similar in Round 1 and 2, but increased above
the 2L Standard in Round 2.
• AI4D — chromium concentrations were similar in Round 1 and 2, but increased above
the 2L Standard in Round 2.
The following COls exceeded their regulatory standard or criteria in groundwater samples
collected from wells beneath the dry ash landfill (Phase II) in both Rounds 1 and 2: antimony,
barium, boron, chromium, cobalt, hexavalent chromium, iron, manganese, pH, selenium,
15
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
sulfate, TDS, and vanadium. This list of COls is consistent with the COls reported in CAP
Part 1.
Groundwater sample results from monitoring wells located beneath the dry ash landfill (Phase
11) for Round 1 and 2 are presented in Table 2-9.
Downgradient and East of Ash Basin and Dry Ash Landfill (Phase 1)
Round 2 groundwater sample results for locations downgradient and east of the ash basin and
dry ash landfill (Phase 1) were generally similar to or less than Round 1 results.
The following COls exceeded their regulatory standard or criteria in groundwater samples
collected from wells downgradient and east of the ash basin and dry ash landfill (Phase 1) in
Rounds 1 and 2: barium, beryllium, boron, chloride, chromium, cobalt, hexavalent chromium,
iron, manganese, pH, thallium, TDS, and vanadium. This list of COls is consistent with the COls
reported in CAP Part 1.
Groundwater sample results from monitoring wells located downgradient and east of the ash
basin and dry ash landfill (Phase 1) for Round 1 and 2 are presented in Table 2-10.
Downgradient and Southeast of Ash Basin
Round 2 groundwater sample results for locations downgradient and southeast of the ash basin
were generally similar to or less than Round 1 results with the exceptions noted below.
• GWA-1 D —turbidity increased above 10 NTU during Round 2. Therefore, cobalt, iron,
and manganese increased to concentrations that exceeded their 2L Standards or IMAC
during Round 2.
Voluntary monitoring wells MW-6D, MW-71D, MW-8S, MW-8D, MW-9S, and MW-91D were
sampled during Round 2, but not Round 1. Sample results from these monitoring wells exhibited
concentrations of COls exceeding regulatory standards similar to those observed in other
monitoring wells sampled during Round 1 downgradient and southeast of the ash basin.
The following COls exceeded their regulatory standard or criteria in groundwater samples
collected from wells downgradient and southeast of the ash basin in Rounds 1 and 2: antimony,
arsenic, boron, cobalt, hexavalent chromium, iron, manganese, pH, thallium, TDS, and
vanadium. This list of COls is consistent with the COls reported in CAP Part 1.
Groundwater sample results from monitoring wells located downgradient and southeast of the
ash basin for Round 1 and 2 are presented in Table 2-11.
2.3.2.3 Description of Groundwater Quality Standard Exceedances
Per CAMA, the CAP should include "A description of all exceedances of the groundwater quality
criteria, including any exceedances that the owner asserts are the result of natural background
conditions." To address this requirement, COls identified during the Round 1 and Round 2
sampling events were evaluated to assess if they are naturally occurring or attributable to ash
handling at the site.
16
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
Results of the COI evaluations are summarized in Table 2-12. Only analytical results that
exceeded their respective groundwater criteria are presented on this table.
It is important to note that this evaluation only includes two sampling events and additional
sampling is needed to re-evaluate PPBCs and more appropriately assess COls compared to
PPBCs at the site. Areas with what appear to be source -related exceedances are shown on
Figure 2-5.
2.3.3 Surface Water and Area of Wetness
During the Round 2 sampling event, two AOWs and seven surface water locations were
sampled at the MSS site. An AOW is defined as an area of ponded or flowing water that is not
attributable to stormwater runoff. Surface water and AOW sample locations are depicted on
Figure 2-1. Round 1 and Round 2 analytical results for the surface water and AOW samples are
presented in Tables 2-13 and 2-14. Sampling locations are listed below.
• AOWs: S-2 and MSSW001
• Surface water: SW-6, SW-7, SW-8, SW-9, SW-10, SW-11, and MSWW002
2.3.3.1 Surface Water
Surface water samples were collected during Round 1 and Round 2. Surface water samples
SW-7 through SW-11 were not sampled during the CSA (Round 1) sampling event. The Round
2 sample results for these surface water samples were evaluated and provided in CAP Part 1.
Round 2 surface water sample results were generally similar to or less than Round 1 results
except that sulfate exceeded its 2B Standard in SW-6 in Round 2. Surface water analytical
results are provided in Table 2-13.
The following COls exceeded their regulatory standard or criteria in surface water samples
collected in Rounds 1 and 2: aluminum, cadmium, cobalt, copper, iron, lead, manganese,
sulfate, and TDS. This list of COls is consistent with the COls reported in CAP Part 1.
2.3.3.2 Areas of Wetness
Round 2 AOW sample results were generally similar to or less than Round 1 results with the
exceptions noted below.
• MSWW001 — iron and vanadium exceeded the 2L Standard and IMAC, respectively, in
Round 2. Concentrations of boron, cobalt, hexavalent chromium, manganese, thallium,
and TDS exceeding regulatory standards from Round 1 were not observed in Round 2.
Turbidity was measured at 1.29 NTU during Round 1 compared to 38.5 NTU during
Round 2.
• S-2 — iron and chloride exceeded their 2L Standards in Round 2. Concentrations of
arsenic, barium, beryllium, chromium, lead, selenium, and vanadium exceeding
regulatory standards from Round 1 were not observed in Round 2. Turbidity was
measured at 986 NTU during Round 1 compared to 9.02 NTU during Round 2.
The following COls exceeded their regulatory standard or criteria in AOW samples collected in
Rounds 1 and 2: arsenic, barium, beryllium, boron, chloride, chromium, hexavalent chromium,
17
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
cobalt, iron, lead, manganese, pH, selenium, thallium, TDS, and vanadium. This list of COls is
consistent with the COls reported in CAP Part 1. Round 1 and Round 2 analytical results for the
AOW samples are presented in Table 2-14.
2.4 Round 3 and Round 4 Background Well Sampling
In response to a Duke Energy request for clarification of guidance, NCDEQ provided a table
titled "Clarification of Attachment 1 Groundwater Assessment Plan Conditional Letters of
Approval Items Related to Speciation — May 22, 2015" by electronic mail.
In the responses provided in this table, NCDEQ requested that Duke Energy "plan to sample the
existing and newly installed background wells two additional times during 2015 as part of an
anticipated corrective action measure to support USEPA tiered site analysis and statistical
analysis". The two additional sampling events referenced in this response correspond to
background sampling Rounds 3 and Round 4, performed in November and December 2015,
respectively.
Groundwater sample collection and analysis were conducted in accordance with procedures
described in the CSA Report. The results of the Round 3 and Round 4 background well
sampling events are presented in Table 2-6. The locations of the background monitoring wells
are presented on Figure 2-1. Further evaluation of background sample results and refinement
of PPBCs will be provided in subsequent reports.
18
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
3 Site Conceptual Model
The SCM was initially presented in the CSA Report, and refined based on results from
additional sampling events, groundwater contaminant fate and transport modeling, and
groundwater to surface water interaction modeling. The SCM for the MSS site was developed in
general accordance with the ASTM standard guidance document E1689-95 (Reapproved 2014),
Standard Guide for Developing Conceptual Site Models for Contaminated Sites (ASTM 2014),
to describe and integrate processes that determine contaminant releases, contaminant
migration, and environmental receptor exposure to contaminants. The SCM is used to integrate
site information and determine whether additional information may be needed to further
understand site hydrogeologic and potential contaminant migration processes. The model is
also used to support selection of remedial alternatives and effectiveness of corrective actions in
reducing the potential exposure of environmental receptors to contaminants. The SCM was
developed using the six basic activities outlined in ASTM E1689-95:
• Identification of potential contaminants
• Identification and characterization of the source(s) of contaminants
• Delineation of potential migration pathways through environmental media
• Establishment of background areas
• Environmental receptor Information
• Determination of system boundaries
An expanded discussion of site geochemical controls on contaminant mobility and migration is
also provided, as requested by NCDEQ. A graphical representation of the SCM is included as
Figure 3-1.
3.1 Identification of Potential Contaminants
Potential contaminants (COls) were identified in the CSA Report and are summarized in
Section 2.1 of this report.
3.2 Identification and Characterization of Source
Contaminants
The source areas at MSS are defined as the ash basin, the dry ash landfill (Phases I and II),
and the PV structural fill (Figure 2-1). Source characterization was performed through the
completion of soil and rock borings, installation of monitoring wells, and collection and analysis
of associated solid matrix and aqueous samples to identify physical and chemical properties of
ash, ash basin water, ash porewater, and ash basin AOWs (Figure 3-1). A geologic cross-
section through the source areas is shown on Figure 3-2 (4 sheets). A summary of source
characterization analytical results per sample medium were provided in the CSA Report. Round
1 and Round 2 analytical results for ash porewater and ash basin water are provided in Tables
2-4 and 2-5, respectively.
Ash distribution and chemical and physical properties were evaluated through advancement and
sampling of 23 borings within the ash basin boundary, three borings in the dry ash landfill, and
19
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
eight borings within the PV structural fill boundary. Ash within the ash basin was encountered to
depths ranging from the ground surface to approximately 85 feet below ground surface ( ft bgs).
Ash in the dry ash landfill was encountered from approximately 2 to 111 ft bgs. Ash within the
PV structural fill was encountered beneath the soil cap system to depths ranging from
approximately 28 to 71 ft bgs.
Ash porewater was evaluated through the sampling of 18 monitoring wells installed within the
basin. Ash basin water was evaluated through sampling and analysis of five water samples.
Based on the CSA results, concentrations of COls in groundwater that are attributable to the
source areas are limited to beneath the ash basin, beneath the dry ash landfill (Phase 11),
downgradient and east of the ash basin and dry ash landfill (Phase 1), and downgradient and
southeast of the ash basin. Concentrations of COls in groundwater were higher beneath the dry
ash landfill (Phase 11) and downgradient and east of the ash basin and dry ash landfill (Phase 1)
compared to beneath the ash basin. COI transport is generally in a southeasterly direction
towards Lake Norman and the unnamed tributary that flows to Lake Norman.
Review of laboratory analytical results of ash samples collected from the ash basin, dry ash
landfill (Phase 11), and PV structural fill identified nine COls: antimony, arsenic, barium, boron,
cobalt, iron, manganese, selenium, and vanadium.
COls identified in ash porewater samples include antimony, arsenic, barium, beryllium, boron,
cadmium, chloride, chromium, cobalt, iron, lead, manganese, nickel, selenium, sulfate, thallium,
TDS, and vanadium.
COls identified in ash basin water samples include arsenic, beryllium, boron, cadmium, chloride,
cobalt, copper, lead, manganese, nickel, selenium, sulfate, thallium, TDS, vanadium, and zinc.
3.3 Delineation of Potential Migration Pathways through
Environmental Media
3.3.1 Soil
The soil zone encountered beneath the ash basin ranged from approximately 5.5 to 76 feet.
Generally, there is not an unsaturated soil zone beneath the ash basin to allow for sorption of
COls to occur prior to reaching groundwater.
The soil zone encountered beneath the dry ash landfill (Phase 11) ranged from approximately
34.5 to 78 feet in thickness. An unsaturated soil layer approximately 21 to 23 feet thick was
present beneath portions of the ash landfill; however, the northeast portion of the ash landfill
contained approximately two feet of saturated ash above saturated soil.
The residual unsaturated soil/saprolite zone encountered beneath the PV structural fill was
approximately one to 10 feet thick, which inhibits COls from leaching directly into groundwater.
Based on depth to groundwater measurements directly east of the dry ash landfill (Phase 1),
which was approximately 36 ft bgs during the CSA, there is a high likelihood of an unsaturated
20
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
soil buffer located beneath the dry ash landfill (Phase 1). Note that soil borings were not
advanced within the footprint of the dry ash landfill (Phase 1).
3.3.2 Groundwater
Site hydrogeologic conditions were evaluated through sampling/testing conducted during
installation of 13 borings and 83 monitoring wells. Based on observations from the CSA
investigation, the groundwater system in the natural materials (alluvium, soil, soil/saprolite, and
bedrock) at MSS is consistent with the regolith-fractured rock system and is an unconfined,
connected aquifer system. The MSS groundwater system is divided into three layers referred to
as the shallow, deep (transition zone), and bedrock flow layers to distinguish the flow layers
within the connected aquifer system.
In general, groundwater within the shallow, deep, and bedrock layers flows from the north and
northwest extents of the MSS site to the south and southeast toward Lake Norman. Monitoring
wells installed outside the northwest, north, and northeast boundaries of the ash basin indicate
that groundwater flows toward the ash basin along the west and north property boundaries.
Shallow and deep groundwater at the site discharges to Lake Norman and an unnamed
tributary that flows to Lake Norman east of the ash basin and dry ash landfill (Phase 1).
Groundwater flows from the southeast portion of the ash basin to the east and beneath the dry
ash landfill (Phase 1), and ultimately toward the unnamed tributary that flows to Lake Norman.
Between the ash basin and Lake Norman (i.e., the southernmost portion of the ash basin),
groundwater flows to the south/southeast toward Lake Norman. Groundwater flow direction in
the shallow, deep and bedrock flow layers is shown on Figure 2-2, 2-3, and 2-4, respectively.
3.3.3 Surface Water and Sediment
During the CSA, one surface water sample (SW-6) was obtained from the unnamed tributary
east and downgradient of the dry ash landfill (Phase 1) and the ash basin. In addition, two
upgradient surface water samples (SW-7 and SW-8) were collected from perennial streams that
flow toward the ash basin and PV structural fill, and three surface water samples (SW-9, SW-10,
and SW-1 1) were collected from Lake Norman downgradient of the ash basin and dry ash
landfill (Phase 1).
In general, COls identified in surface water sample SW-6, collected from the unnamed tributary
to Lake Norman, are similar to groundwater COls identified in monitoring wells located between
the unnamed tributary and the dry ash landfill (Phase 1) and ash basin. This supports the need
for further evaluation of the COls identified in the SW-6 sample.
Of the COls identified in the surface water samples collected from Lake Norman, manganese is
the only COI that exceeded its 2L Standard or IMAC in groundwater monitoring wells located
between the ash basin and Lake Norman. Cadmium, copper, and lead were identified as
source -related COIs in the CSA and exceeded their 2B Standards in Lake Norman. However,
these constituents were not detected above their 2L Standards in groundwater monitoring wells
located between the ash basin and Lake Norman, indicating that there is not a complete
pathway of exceedances of these constituents from the ash basin to Lake Norman. Note that
21
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
the 2B Standards for cadmium, copper, and lead are more than one order of magnitude less
than their 2L Standards.
3.4 Establishment of Background Areas
The background locations at MSS are located on the northeast side of the site. As described in
the CAP Part 1, wells determined to represent background conditions at the site are compliance
monitoring wells MW-4 and MW-4D, FGD Residue Landfill monitoring well MS-10, and CSA
background monitoring wells BG-1 S/D, BG-2S/BR, and BG-3S/D. A detailed background
monitoring well assessment is presented in CAP Part 1 Report, Appendix B.
3.5 Environmental Receptor Identification and Discussion
Duke Energy conducted a receptor survey of the area within 0.5 miles of the ash basin
Compliance Boundary in September 2014, and supplemented the receptor survey in November
2014. Locations of receptors identified during the surveys are shown on Figure 3-3.
Properties located within a 0.5-mile radius of the MSS ash basin Compliance Boundary
generally consist of undeveloped land and Lake Norman to the east, undeveloped land and
residential properties to the north and west, portions of the MSS site outside the Compliance
Boundary, undeveloped land and residences to the south, and commercial properties to the
southeast along North Carolina Highway 150.
The receptor survey activities identified four public water supply wells and 83 private water
supply wells in use, along with six assumed private water supply wells, located within the 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 Sherrills Ford Road toward Lake Norman were
identified within a 0.5-mile radius of the ash basin Compliance Boundary. No water supply wells
(including irrigation wells and unused or abandoned wells) were identified between the source
areas and Lake Norman.
3.6 Determination of System Boundaries
The site boundary, waste boundaries, and Compliance Boundary at the MMS site are depicted
on Figure 2-1. Spatially, the SCM for MSS is bounded by Lake Norman to the southeast, which
is a hydrologic boundary, and topographically and hydrologically elevated areas west and north
of the ash basin system. The SCM extends vertically into bedrock.
3.7 Site Geochemistry and Influence on COls
Groundwater composition can be affected by an array of naturally -occurring and anthropogenic
factors. Many of these factors can be causative agents for specific reduction -oxidation (redox)
processes or indicators of the implied redox state of groundwater as expressed by pH,
oxidation-reduction potential (ORP), and dissolved oxygen. Groundwater pH is affected by the
composition of the bedrock and soil through which the water moves as well as other factors,
including exposure to carbonate rocks or lime -containing materials in well casings, exposure to
atmospheric carbon dioxide gas, and precipitation. In addition, metals and other elemental or
22
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
ionic constituents in groundwater, or the surrounding soil matrix, can act as electron donors or
acceptors as measured by ORP. The reactivity of different constituents can lead to oxidizing
(positive ORP) or reducing (negative ORP) environments in groundwater systems. DO in
groundwater can act as an oxidizing agent and is an indicator of redox state.
Based on field measurements, the primary redox categories at the MSS site were determined to
include oxic, suboxic, mixed (oxi-anoxic), mixed (anoxic), and anoxic conditions. At MSS, DO
levels exceeded the threshold of 0.5 mg/L in 66 of 91 samples (72%) and predominant redox
processes are oxygen reduction with iron or manganese oxidation (i.e., controlled by 02 and
Fe(III)/Fe(II) or Mn(IV)/Mn(II) couples). Under these conditions, more oxidized species As(V),
Se(VI), and Mn(IV) would be expected. There were 18 wells from which ash porewater samples
were collected and 17 of those samples are classified as anoxic or mixed (oxi-anoxic); one
sample was classified as suboxic. There is an increased potential for reduced forms of metals to
occur under anoxic or mixed conditions. However, it should be noted that 33 of the 73 (-45%)
groundwater samples from wells across the site are classified as suboxic or oxic categories
where reduced species of metals such as As(III) are less likely to be present.
Field measurements indicate that pH ranges from 4.5 to 11.9 SU in groundwater at the site.
Background well results indicate that pH ranges from 5.7 to 10.9 SU. Similarly, pH results for
upgradient wells beyond the waste boundary range from 5.4 to 11.9 SU. In contrast, pH values
within ash porewater range from 2.8 to 8.5 SU. pH values in groundwater downgradient of the
source areas range from 4.5 to 11.2 SU. There is a very wide range of ORP values, spanning
ranges that imply reduced (negative values) to highly oxidized (large positive values) conditions.
For ash porewater, reducing conditions are present throughout the ash basin except for the
southwest portion of the ash basin. For groundwater, oxidizing conditions are generally present
in the deep flow layer beneath the ash basin, dry ash landfill (Phase II), and PV structural fill.
Reducing conditions are present in groundwater in several locations including AB-6D, AB-8D,
AB-15D, AB-16D and all bedrock wells installed beneath the ash basin.
For the three background well samples, ORP values are generally consistent with the inferred
redox category of mixed (oxic-anoxic). In contrast, measured ORP values from non -background
monitoring wells ranged from -148 mV (reducing) to +597 mV (strongly oxidizing), whereas
inferred redox conditions were generally mixed (oxic-anoxic). Positive ORP values measured in
samples where mixed (oxic-anoxic) conditions are inferred suggest that many samples may not
be in redox equilibrium.
Speciation measurements were performed for samples collected from 25 groundwater and/or
ash porewater monitoring wells, depending on the analyte, and vary widely at the site.
Speciation measurements are summarized below:
For the five samples where speciated arsenic concentrations were above reporting
limits, the predominant species was the reducing form As(III), representing 68% of the
total arsenic.
• In general, Cr(VI) was identified in upgradient and background groundwater samples
with higher concentrations than those collected from ash porewater wells and
groundwater monitoring wells beneath and downgradient of the on -site source areas.
23
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
• The reduced form of iron [Fe(II)] was mainly present downgradient and southeast of the
ash basin.
• The reduced form of manganese [Mn(II)] was mainly present beneath the central portion
of the ash basin and downgradient and southeast of the ash basin.
The reduced form of selenium [Se(IV)] was present above detection limits in just one
sample. The oxidized form of selenium [Se(VI)] was present above detection limits in five
samples. Se(VI) was present beneath the central portion of the ash basin (AB-12D) and
in one deep background well (BG-1 D). The highest concentrations of Se(VI) were
reported in two wells located downgradient and east of the ash basin and dry ash landfill
(Phase 1) (MW-14S and MW-14D).
Piper diagrams were generated as part of the CSA to compare geochemistry between ash basin
porewater and groundwater. In general, the ionic composition of upgradient and background
groundwater at the site is less chloride- and sulfate -rich than ash basin porewater, ash basin
water, and downgradient groundwater, which were observed to be trending closer to calcium-,
chloride-, magnesium-, and sulfate -rich.
24
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
4 Modeling
4.1 Groundwater Model Refinement
The groundwater flow and contaminant fate and transport models were refined to incorporate
post-CSA data. Model refinements are summarized below. The refined groundwater flow and
contaminant fate and transport model reports were completed by HDR in conjunction with the
University of North Carolina at Charlotte (UNCC). An independent review of the refined MSS
model was conducted by the Electric Power Research Institute (EPRI) and found that the model
was set-up and meets its flow and transport calibration objectives sufficiently to meet its final
objective of predicting effects of corrective action alternatives on groundwater quality. The
refined groundwater flow and transport model report and the EPRI review of the calibrated MSS
model are provided in Appendix B.
4.1.1 Flow Model Refinements
Transient transport simulations for all modeled COls were calibrated and flow parameters were
refined as follows:
Hydraulic conductivity measurements, obtained from slug test data collected during the
CSA, were utilized in the calibration of the flow model to better represent site -specific
conditions. This refinement led to reduction in the square root of the average square
error (also referred to as the root mean squared error) of the modeled versus observed
water levels for wells gauged in July 2015 to 4.68% compared to the initial calibrated
model root mean squared error of 5.75% in the difference in head between the modeled
and the observed values across the model domain. These results are provided in Table
3 in Appendix B.
• Recharge rates for the model were revised within and outside of the ash basin.
Recharge applied to the inactive portion of the ash basin and areas outside the ash
basin were assigned a value of 6.6 inches per year. The dry ash landfill (Phase 1),
Industrial Landfill No. 1 and The FGD Residue Landfill were constructed with liners, and
as a result the recharge was set to zero in these areas. The calibrated model recharge
at the PV structural fill and dry ash landfill (Phase 11) were set at 6.6 and 4.0 inches per
year, respectively. Recharge within the active portion of the ash basin was calculated
using Darcy's Law and is based on the area of the ash basin, the approximate depth of
water or saturated ash, and the range of measured hydraulic conductivity values within
the ash. The recharge rate applied to the active portion of the ash basin area was set at
12.3 inches per year.
Historic basin water levels were considered during calibration of the flow model.
However, the current flow model is calibrated to steady-state conditions. Continued
refinement of the model to consider transient flow may enhance integration of historic
water level data within the ash basin.
• The bedrock hydrostratigraphic layers were extended vertically in the refined model to
correlate to the deepest reported off -site private water supply well, as obtained from the
25
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
completed questionnaires received from adjacent well owners during the receptor survey
conducted in 2015 and/or the North Carolina State/Gaston or Mecklenburg County
geographic information system (GIS) database.
Private water supply wells were identified in the CSA Report. Residential wells were
identified at four locations within the current model domain. Potential effects on the site -
specific flow regime from pumping of these wells were simulated by applying a constant
pumping rate of 400 gallons per day (gpd), which represents the average household
usage per USEPA Water Sense Partnership Program (USEPA 2015a).
4.1.2 Contaminant Fate and Transport Model Refinements
The groundwater contaminant fate and transport model was calibrated using the refined
parameters from the groundwater flow model, as discussed in Section 4.1.1, and presented
below.
The initial model used conservative (low) sorption coefficient (Kd) values to achieve
calibration of the contaminant fate and transport models for each COI. Subsequent to
submittal of the CAP Part 1 Report, Kd values were recalculated using linear and
Freundlich isotherms (Appendix C). Refinement of the flow model and use of the newly
derived upper and lower Kd limits in the contaminant fate and transport model resulted in
improved calibration of source concentrations to measured concentrations in
downgradient wells. Note that final Kd values used to calibrate the fate and transport
models may have fallen outside the recalculated upper and lower limits; however,
adjustment of Kd values within the model to achieve calibration is considered acceptable
practice.
• The initial contaminant fate and transport model used adjusted source area
concentrations to achieve calibration at downgradient monitoring wells. The flow model
refinements discussed in Section 4.1.1 enabled refinement of the contaminant fate and
transport model to better represent measured source area ash porewater
concentrations.
• The initial contaminant fate and transport model was not calibrated to background
groundwater concentrations as PPBCs were not developed in time for use in the model.
The model has since been refined to incorporate background concentrations (i.e.,
PPBCs) for each COI. This refinement allows the models to account for naturally
occurring background concentrations and is particularly important for COls with a PPBC
greater than the 2L Standard, IMAC, or NCDHHS HSL. However, the model is limited in
that it applies the PPBC across the entire site, as shown on individual COI concentration
figures in Appendix B.
• Round 2 laboratory analytical data were reviewed and no additional COls were identified
for including in the refined modeling efforts.
• Potential COI impacts to private water supply wells located within the current model
domain were evaluated through reverse particle tracking simulations by applying a
constant pumping rate of 400 gallons per day at each well, as specified in Section 4.1.1.
26
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
Particle tracking simulations show advective travel time and do not account for reduced
travel time associated with sorptive COls (i.e., arsenic).
Refinements to the groundwater model in CAP Part 2 provide a more accurate representation of
existing site conditions, which produces model results that more accurately simulate the
proposed closure scenarios at the MSS site.
4.1.3 Summary of Modeled Results
Two closure scenarios were modeled for MSS: an Existing Conditions scenario with ash
sources left in place and a Cap -In -Place scenario, which simulates the effects of covering the
ash basin at the beginning of the predictive simulation with an engineered cap. These
simulations predict flow and transport results and are calibrated for existing conditions. Once the
chosen scenario is decided on for corrective action, the model should be revised and
recalibrated to improve its accuracy and reduce uncertainty.
4.1.3.1 Existing Conditions Scenario
The Existing Conditions scenario consists of using the calibrated model for steady-state
groundwater flow conditions and transient transport of COls under existing conditions across the
site to predict when steady-state concentrations are reached at the Compliance Boundary. COI
concentrations remain the same for this scenario with source concentrations being held at their
constant value over time. This scenario represents the most conservative case in terms of
groundwater concentrations on -site and off -site, with COls discharging to surface water at
steady-state.
The time to achieve a steady-state plume depends on location of the source areas relative to
the Compliance Boundary and the COI loading history. Areas close to the Compliance
Boundary will reach a steady-state concentration sooner. The time to steady-state concentration
is also dependent on the sorptive characteristics of each COI. Sorptive COls are transient for a
longer time period as their peak breakthrough concentration travels at a rate that is less than
groundwater pore velocity. Use of lower effective porosity results in shorter times to achieve
steady-state concentrations for both sorptive and non-sorptive COls.
4.1.3.2 Cap -in -Place Scenario
The Cap -in -Place scenario simulates the effects of covering the ash basin at the beginning of
the predictive simulation with an engineered cap. In the model, recharge at the ash basin is set
to zero. In the model, non-sorptive COls move downgradient at the pore velocity of groundwater
and are displaced by the passage of a single ash porewater volume, while sorptive COls
migration in groundwater is retarded because of sorption with soil/rock. The model uses the
predicted concentration from the 2015 calibration as the initial concentration at the start of the
model scenario.
COls move through the saturated zone beneath the source areas at a rate dependent on aquifer
properties and geochemical interactions of the COI and groundwater. If the source areas
become unsaturated, concentrations of COls beneath the source zones will decrease over time
without a contributing constant source.
27
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
Groundwater flow is affected by this scenario as the water table is lowered, and groundwater
velocities are reduced beneath the capped areas. The water table just upgradient of the ash
basin dike in the ash basin was reduced by approximately 10 feet. In the ash basin between the
PV structural fill and dry ash landfill (Phase II), the water table was reduced by approximately 1
foot.
4.1.4 Model Assumptions and Limitations
The model assumptions include the following:
• The steady-state flow model was calibrated to hydraulic heads measured at observation
wells in July 2015 and reflects the ash basin water level. The model is not calibrated to
transient water levels over time, recharge, or stage changes in Lake Norman. A steady-
state calibration does not consider groundwater storage, and was not used to calibrate
the groundwater flux into adjacent surface water bodies.
• A single domain MODFLOW modeling approach was used for simulating flow in the
primary porous groundwater flow layer and bedrock for contaminant transport at the
MSS site. MODFLOW simulates flow through porous media and groundwater flow in the
bedrock zone via fractures in the bedrock.
• The model was calibrated by adjusting the constant source concentrations at the ash
basin and ash storage areas to reasonably match 2015 COI concentrations in
groundwater.
• For the purposes of numerical modeling and comparing closure scenarios, it was
assumed that the selected closure scenario was implemented in 2015.
• Predictive simulations were performed and steady-state flow conditions were assumed
from the time the ash basin and ash storage areas were placed in service (Year 1965)
through the current time until the end of the predictive simulations (Year 2265).
• COI source area concentrations were applied uniformly within each source area and
assumed to be constant with respect to time for transport model calibration.
• The background concentrations for the COls were applied as initial concentrations.
• Travel times are advective and do not account for sorption of COls to site media, which
may cause the travel times to be reduced.
• Residential wells are assumed to have a constant pumping rate of 400 gpd and are
completed in bedrock.
• The model does not account for varying geochemical conditions such as pH and redox
potential that could affect COI mobility; however, geochemical modeling was completed
and is further discussed in Section 4.3.
4.1.5 Modeled Scenario Results
Constituent concentrations were analyzed at downgradient monitoring wells (Figure 7 in
Appendix B) for all modeled COls. These wells are downgradient from the ash basin and
upgradient of the ash basin Compliance Boundary at Lake Norman. Wells AB-1 S and AB-2S
28
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
are located on the ash basin dam, while GWA-1 S is near the southeastern corner of the main
coal storage area, and MW-6 is northeast of the ash basin dam and directly east of the dry ash
landfill (Phase 1).
Closure scenario results are presented as predicted concentration versus time curves in
downgradient monitoring wells and as groundwater concentration maps for each of the 13
modeled COls on Figures 16 through 184 of Appendix B, as discussed in the following sub-
sections. Concentration contours and concentration breakthrough curves are referenced to
1965, the year that the ash basin became active. Groundwater concentration maps are
referenced to a time zero that represents the time the closure action planned to be
implemented, which for the purposes of modeling is assumed to be 2015.
A summary of the modeled COI results is provided below in Table 4-1. A "+" indicates that the
predicted concentration of a given COI exceeds its applicable 2L Standard, IMAC, or NCDHHS
HSL at the Compliance Boundary. A " ° indicates that the concentration of a given COI has not
exceeded its applicable 2L Standard, IMAC, or NCDHHS HSL at the Compliance Boundary.
Year 0 indicates the time the closure action was implemented (2015), and Year 100 indicates
100 years from the time the closure action was implemented (2115).
Table 4-1 Summary of Modeled COI Results
Constituent
(Standard)
Appendix B
Figures
Flow Layer
Existing Conditions
Cap -in -Place Scenario
Year 0
Year 100
Year 0
Year 100
Antimony
IMAC
(1 pg/L)
16 - 28
Shallow
+
+
+
+
Deep
+
+
+
+
Bedrock
+
+
+
+
Arsenic
2L
(10 pg/L)
29 - 41
Shallow
-
-
-
-
Deep
-
-
-
-
Bedrock
-
-
-
-
Barium
2L
(700 pg/L)
42 - 54
Shallow
-
-
-
-
Deep
-
-
-
-
Bedrock
-
-
-
-
Beryllium
IMAC
(4 pg/L)
55 - 67
Shallow
-
+
-
-
Deep
-
+
-
-
Bedrock
-
-
-
-
Boron
2L
(700 pg/L)
68 — 80
Shallow
+
+
+
+
Dee
+
+
+
+
Bedrock
+
+
+
+
Chloride
2L
(250,000 pg/L)
81 - 93
Shallow
-
-
-
-
Deep
-
-
-
-
Bedrock
-
-
-
-
Chromium
2L
(10 pg/L)
94 - 106
Shallow
+
+
+
+
Deep
+
+
+
+
Bedrock
+
+
+
+
Cobalt
IMAC
(1 pg/L)
107-119
Shallow
+
+
+
+
Deep
+
+
+
+
Bedrock
+
+
+
+
Hexavalent
Chromium
120-132
Shallow
+
+
+
+
Deep
+
+
+
+
29
Corrective Action Plan Part 2
Marshall Steam Station Ash Basin
Constituent
(Standard)
NCDHHS HSL
0.07 /L
Appendix B
Figures
Flow Layer
Existing Conditions
Cap -in -Place Scenario
Year 0
Year 100
Year 0
Year 100
Bedrock
+
+
+
+
Selenium
2L
(20 pg/L)
133-145
Shallow
-
-
-
-
Deep
-
-
-
-
Bedrock
-
-
-
-
Sulfate
2L
(250,000 pg/L)
146-158
Shallow
-
-
-
-
Deep
-
-
-
-
Bedrock
-
-
-
-
Thallium
IMAC
(0.2 pg/L)
159 - 171
Shallow
+
+
+
+
Deep
+
+
+
+
Bedrock
+
+
+
+
Vanadium
IMAC
(0.3 pg/L)
172 - 184
Shallow
+
+
+
+
Deep
+
+
+
+
Bedrock
+
+
+
+
The model predictions are summarized as follows:
In accordance with 15A NCAC 02L.0106 (k), a CAP may be approved by NCDEQ
without requiring groundwater remediation to the 2L Standards if certain conditions are
met. Condition (4) specifies that 2L Standards must be met at a location no closer than
one year time of travel upgradient of an existing or foreseeable receptor. For MSS, the
receptor is considered to be the four nearby residential pumping wells north of the steam
station that are included in the model domain. To evaluate this condition, HDR and
UNCC conducted particle tracking within the Existing Conditions scenario steady-state
flow field to identify the one-year travel time boundary. The residential pumping wells
were set to pump at a rate of 400 gpd (representing the average USEPA daily household
usage rate). The advective travel time one year from each well was performed using
MODPATH (shown on Figure 15 in Appendix B). The one-year advective travel time
pathlines do not intersect the Compliance Boundary.
The refined model predicts that under the Existing Conditions and Cap -in -Place
scenarios, antimony, beryllium, boron, chromium, cobalt, hexavalent chromium, ,
thallium and vanadium are predicted to exceed their respective 2L Standards or IMACs
at the model interface (i.e., Lake Norman and the unnamed tributary) or the Compliance
Boundary for all groundwater flow layers. Also, hexavalent chromium is predicted to
exceed the NCDHHS HSL at Lake Norman for all groundwater flow layers. For these
COls, the background concentrations used for modeling antimony, chromium, cobalt,
hexavalent chromium, thallium, and vanadium also exceed the applicable groundwater
standards, so the actual impact of the site sources on groundwater quality is unknown.
The background concentration used to model boron was less than the 2L Standard and
the modeling predicts that boron will exceed its 2L Standard at the model interface or
Compliance Boundary.
30
Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
• The model predicts that under the Existing Conditions and Cap -in -Place scenarios,
arsenic, barium, chloride, selenium, and sulfate are not predicted to exceed the
applicable groundwater standards at the model interface or Compliance Boundary.
4.2 Surface Water Model Refinement
4.2.1 Methodology
The methodology to complete the surface water model in CAP Part 2 (Appendix D) is
consistent with CAP Part 1 and incorporates new groundwater modeling results addressed in
Section 4.1 including:
• Refinement of Kd values.
• Updated groundwater flux data for input into the surface water model.
Groundwater to surface water interactions were evaluated using groundwater model output and
a surface water mixing model approach to evaluate potential surface water impacts of COls in
groundwater as they discharge to surface water bodies adjacent to the MSS site.
4.2.2 Results
The calculated surface water COI concentrations in Lake Norman adjacent to and downstream
of the MSS site are presented below in Table 4-2. The design flows, upstream surface water
concentrations, groundwater flows, and groundwater COI concentrations presented in
Appendix B were used to complete these calculations. The mixing model results indicate that
no surface water quality criteria are exceeded for COls modeled at the edge of the mixing zone
in Lake Norman. Descriptions of the mixing zones are provided in Appendix D.
Table 4-2. Lake Norman Calculated Surface Water Concentrations
Calculated Mixing Zone Conc. (Ng/L)
Water Quality Standard (Ng/L)
COI
Acute
Chronic
HH/WS
Acute
Chronic
HH / WS
Arsenic
0.260
0.252
0.251 (c)
340
150
10 / 10
Barium
4.58
4.32
4.32 (nc)
ns
ns
200,000 / 1,000
Beryllium
0.103
0.101
0.100*
65
6.5
ns / ns
Boron
26.9
25.4
25.2*
ns
ns
ns / ns
Chloride
560
432
432 (nc)
ns
ns
ns / 250,000
Total Chromium
0.269
0.254
0.252*
ns
ns
ns / ns
Chromium VI
0.253
0.251
0.250*
16
11
ns / ns
Cobalt
0.255
0.251
0.251 (nc)
ns
ns
4/3
Selenium
0.265
0.253
0.251*
ns
5
ns / ns
Sulfate
660
532
532 (nc)
ns
ns
ns / 250,000
Thallium
0.051
0.050
0.050 (nc)
ns
ns
0.47 / 0.24
Notes:
1. All COls are shown as dissolved fraction except for total chromium, which is total recoverable metal
2. WS — water supply (15A NCAC 02B .0216, amended effective January 1, 2015)
3. HH — human health (15A NCAC 02B .0211, amended effective January 1, 2015)
4. c — carcinogen
5. nc — non -carcinogen
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6. ns — no water quality standard
7. *—calculated for 100% of induced flow
4.3 Geochemical Modeling
4.3.1 Objective
Geochemical modeling was conducted to describe the speciation of COls and other
groundwater constituents across the spectrum of groundwater conditions measured at the MSS
site. The objective of geochemical modeling is to describe the expected partitioning of COls
between aqueous and solid phases (i.e., between groundwater and soil and between ash
porewater and ash) and anticipated changes in phase distributions given variations in DO, pH,
and TDS. Changes in DO will affect the oxidation state of groundwater as measured by ORP,
which is generally expressed as Eh or electron activity (pE). Changes in pH affect the acidity of
groundwater and concurrently affect Eh. Changes in TDS affect ionic strength and ion
competition at sorption sites. Constituents evaluated for MSS were: antimony, arsenic, barium,
beryllium, boron, chloride, chromium, cobalt, iron, lead, manganese, nickel, selenium, sulfate,
thallium, and vanadium.
4.3.2 Methodology
Site -specific evaluations of COls were performed for each of the monitoring wells using the U.S.
Geological Survey (USGS) PHREEQC (0.3.3) geochemical speciation code (Parkhurst and
Appelo 2013) and PhreePlot (Kinniburgh and Cooper 2011), a companion plotting package that
utilizes looping PHREEQC with a hunt and track approach to determine stability boundaries. By
using a single well approach, wells can be evaluated or grouped later based on geochemical
characteristics. The single well approach also allows fine resolution of geochemical constituents
and subtle differences between wells that have a significant bearing on the overall geochemical
characterization. Calculations were driven by measured concentrations of COls and other
analytes such as ORP (also described as Eh), alkalinity, sodium, and other ions in groundwater
for each of the 101 wells monitored at the site.
PHREEQC calculations were performed to construct Pourbaix (Eh -pH) diagrams to display the
dominant geochemical forms (i.e., species) that would be expected in groundwater in the
absence of adsorption under equilibrium conditions and allowing for most probable mineral
precipitation where appropriate. Measured ORP (presented as Eh) and pH values for each well
were plotted on the Pourbaix diagram for each COI to evaluate the likely distribution of species
at the MSSI site. Additional PHREEQC calculations were performed to simulate anticipated
geochemical speciation that would occur for each COI in the presence of adsorption to soils.
Further simulations were performed to evaluate model and COI response to changes in DO, pH,
and TDS in the presence of sediment adsorption. Adsorption to soils was represented using a
surface complexation theory approach with hydrous ferric oxides (HFO) and hydrous aluminum
oxides (HAO) representing weak and strong binding sites, respectively. Values for HFO and
HAO were determined from actual site sediment extractions that were also the basis for
measured distribution coefficients (Kd values) for site soils determined from adsorption
experiments conducted by UNCC.
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In order to geochemically simulate changes to aquifers or test potential remediation strategies,
DO, pH, redox, and TDS were varied in the simulations. These geochemical simulations are
termed titrations for this report. Each set of titrations provides an estimate of the percentage of
each COI that would be adsorbed as a function of changing DO, pH, reduction -oxidation
(redox), or TDS along with relevant changes to the dominant species across the gradient. For
these titrations, TDS was evaluated as the addition of a select set of cations and anions known
to be common in soils and sediment at the MSS site to include sodium, calcium, chloride,
potassium, and sulfate. Changes to DO, pH, and TDS were utilized for titrations due to the
affinity for numerous COls such as metals to exist primarily as anionic or cationic species and
their adsorption coefficient variations to mineral surfaces, soils, sediment, rock and ash. The
titration method in geochemical modeling can also account for mobility changes due to redox
threshold changes as well and potential mineral precipitation, indicated by saturation indices in
outputs. Adsorption of anionic species is typically greater at lower pH where anions are more
strongly attracted to positively charged surfaces (and vice versa regarding cationic species).
Similarly, the solubility of mineral phases is pH dependent and lower pH levels tend to favor
formation of more soluble cationic species for most alkali elements, alkali earth elements, and
transition metals. Geochemical modeling methodologies are discussed in further detail in
Appendix E.
4.3.3 Assumptions
The following assumptions apply to PHREEQC modeling efforts for the MSS site:
• Groundwater data evaluation based on an individual well basis.
• COI sorption in PHREEQC was represented by surface complexation. Surface
complexation models provide a molecular description of adsorption using an equilibrium
approach that defines surface species, chemical reactions, equilibrium constants, mass
and charge balances. A benefit of the surface complexation approach is that the charge
on both the adsorbing ion and the solid surface where sorption occurs.
• The surface complexation model was parameterized based on soil column tests and
extraction measurements reported by UNCC. The range of sorption properties was
parameterized as the minimum, mean, and maximum estimates for binding sites as
defined from soil extraction measurements. This range of sorption capacities was used
to develop pH, Eh, DO, TDS, and COI titrations.
• The dominant attenuation process is adsorption to hydrous metal oxides, particularly
HFO and HAO, which are representative of clay minerals and similar facies that are
abundant in soil, transition zone, and bedrock.
• COI concentrations used in PHREEQC model were as reported in the database.
Analytical results qualified as non -detects or estimated values (U- and J-flagged values)
were used as reported without modification.
• Nitrogen values were assumed to be primarily nitrate and alkalinity results were
assumed to be primarily bicarbonate, not carbonate.
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• TDS was evaluated as a summary of calcium, sodium, potassium, magnesium, sulfate,
and chloride ions. These constituents account for approximately 60% of the TDS value.
Chloride does not have sorption constants, so this constituent was addressed as a
component of TDS.
• Eh/pH diagrams and/or predominance plots were developed in PhreePlot or
Geochemist's Workbench for each COI to aid in demonstration of changes in Kd, pH,
and DO.
4.3.4 Geochemical Model Results
The modeling effort described above provides both qualitative and quantitative estimations of
the chemical speciation and adsorption behavior of several key COls. Relevant observations
from this modeling effort are as follows:
• Redox conditions vary widely at the MSS site, indicating that it has not reached
equilibrium, or data is not representative of the conditions sampled. Additional
groundwater results will assist in refining the model further or confirm these findings
should sampling data not be representative of actual groundwater conditions.
• The observed site condition of limited solubility of arsenic, chromium, and cobalt in MSS
site groundwater is confirmed by the modeling.
• Each of the pH, Eh, and TDS figures can be further evaluated to potentially support MNA
or remediation. The addition of an engineered cap would reduce infiltration and
introduction of oxygen presumably creating a more anoxic environment. In addition, pH
adjustment could be performed to make COls less soluble, thus limiting COI migration
during excavation and the release of TDS and other metals.
• Methods such as capping could change groundwater flow, inhibit current microbial
reduction mechanisms, or cause secondary metal redox reductions that could be
modeled when options are chosen more specifically.
• Soil sorptive capacity for COls such as boron is typically small and relatively larger for
COls such as arsenic or chromium.
Refer to Appendix E for further details of MSS site geochemical model results.
4.4 Refined Site Conceptual Model
Groundwater and surface water models were revised to address comments from NCDEQ. An
updated SCM is provided on Figure 3-1. Based on review of refined models and the
geochemical model, no revisions are warranted for the SCM at this time.
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5 Risk Assessment
The purpose of the human health and ecological risk assessment is to characterize potential
risks to humans and ecological receptors associated with exposure to the coal ash -derived
constituents that may be present in groundwater, surface water, sediments, soil, and air due to
release(s) from the coal ash basin at the MSS site.
Results of the risk assessment and the information provided on background conditions and
groundwater flow (including fate and transport model results) provided in the CAP reports will
aid in focusing remedial actions which, when implemented, will provide future conditions that are
protective of human health and the environment, as required by CAMA.
The risk assessment was completed using a methodology designed to be consistent with state
and federal guidance. This methodology represents a step -wise process whereby MSS was
evaluated using the following methods:
• Step 1: Develop a conceptual site model (CSM), including receiving media, exposure
pathways, and human and ecological receptors.
• Step 2: Screen analytical data for the applicable site media by comparing screening
values identified in the risk assessment work plan to identify constituents of potential
concern (COPCs).
• Step 3: Develop site -specific human health risk -based concentrations (RBCs) for the
COPCs, derive exposure point concentrations (EPCs), and compare EPCs to RBCs to
draw conclusions about the significance of potential human health risks.
• Step 4: Develop a site -specific baseline ecological risk assessment (BERA) for the
COPCs and, where appropriate, derive RBCs based on the risk assessment results.
5.1 Step 1: Conceptual Site Model
The CSM includes a site description, information on current and anticipated future land uses,
sources, and potential migration pathways through which coal ash -derived COPCs may have
been transported to other environmental media (receiving media), and the human and
environmental receptors that may come in contact with the receiving media. The CSM is meant
to be a living model that can be updated and modified as additional data become available.
Initial CSMs were presented on CSA Report Figure 12-1 (human health) and Figure 12-2
(ecological). Updated CSMs are provided on Figures 2-3 and 2-4 in Appendix F. The CSMs are
intended to identify potential exposure pathways and receptors that may be applicable at the
site.
For MSS, the following receptors and exposure scenarios are identified in the human health
CSM:
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Corrective Action Plan Part 2 F)�
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• Current/future on -site trespasser with potential exposure to dust in outdoor air, soil
remaining post- remediation9, AOW water and AOW soil, on -site surface water, and on -
site sediment;
• Current/future commercial/industrial worker with potential exposure to dust in outdoor
air, soil remaining post-remediation, AOW water and AOW soil, on -site surface water,
and on -site sediment;
• Current/future construction worker with potential exposure to dust in outdoor air, soil
remaining post-remediation, AOW soil and groundwater;
• Current/future off -site resident with potential exposure to on -site groundwater and off -site
surface water as potential sources of potable water;
• Current/future off -site recreational swimmer and waders with potential exposure to off -
site surface water and off -site sediment; and
• Current/future recreational boaters and recreational and subsistence fishers with
potential exposure to off -site surface water and off -site sediment, and fish ingestion for
recreational and subsistence fishers.
The following ecological receptors and exposure scenarios are identified in the ecological CSM:
• Fish and benthic invertebrates with potential exposure to surface water and sediments.
• Aquatic birds with potential exposure to surface water, sediments, fish, and AOW water.
• Aquatic mammals with potential exposure to surface water, sediment, fish, and AOW
water.
Note the habitats where sampling was performed at MSS were considered primarily aquatic;
therefore, the exposure pathways associated with terrestrial receptors were not evaluated for
this site.
5.2 Step 2: Risk -Based Screening
Groundwater, surface water, sediment, and soil data were evaluated during the CSA using risk -
based screening level concentrations for identified COPCs. Risk -based screening level
concentrations of COPCs were revised in the CAP Part 2 based upon additional groundwater,
surface water, sediment, and soil data collected in the Third and Fourth Quarter 2015.
Screening levels are concentrations of constituents in environmental media (e.g., soil)
considered to be protective under most circumstances; their use requires a detailed
understanding of the underlying assumptions in the CSM, including land use and the presence
of sensitive populations. The presence of a constituent in environmental media at
concentrations below the media and constituent -specific screening level is generally assumed
not to pose a significant threat to human health or the environment. If a constituent exceeds the
screening level, it does not necessarily indicate adverse effects on human health or the
s The planned remedy for the ash basin pending NCDEQ risk classification is capping in place; therefore, it is not
anticipated that soil will remain exposed after remedy implementation. It is included in this assessment as a
receiving medium so that the risk -based methods for evaluating this medium in the future are in place.
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environment; rather, it only indicates that additional evaluation may be warranted. Screening
levels are used in this assessment to help in identifying COPCs to be carried forward into the
evaluation of human health and ecological risk at the site.
5.3 Step 3: Human Health Risk Assessment
COPCs were evaluated through a comparison of EPCs to calculated RBCs. The comparison
was made through calculation of risk ratios for cancer and non -cancer effects. The total risk
ratios among all compounds were then summed.
Risk ratios were calculated by first identifying whether COPC RBCs were based on cancer risk
or non -cancer hazard. For RBCs based on cancer risk, the risk ratio for each COPC was
calculated by dividing the EPC by the cancer -based RBC concentration. For RBCs based on
non -cancer risk, the risk ratio for each COPC was calculated by dividing the EPC by the non -
cancer -based RBC concentration.
A risk ratio less than 1 indicated that the EPC does not exceed the RBC, whereas a ratio
greater than 1 indicated that the EPC exceeds the RBC. Risk ratios were also used to evaluate
the cumulative receptor risk associated with each exposure point. Cumulative receptor risk was
calculated by summing the risk ratios among all COPCs on which the RBC was based.
In accordance with USEPA risk assessment guidance (USEPA 1991), the cumulative cancer
risks and non -cancer hazard indices were evaluated against the USEPA target cancer risk
range of 1.0E-06 to 1.0E-04 for potential carcinogens and target non -cancer hazard index of 1
for non -carcinogens (that act on the same target organ by the same mechanism of action);
cumulative cancer risks and hazard indices that are above these limits indicate further
evaluation may be deemed necessary.
For MSS, the results of the human health risk assessment indicate that exposure to on -site
surface water, AOW water, AOW soil, sediment, and groundwater pose no unacceptable risk for
a trespasser, commercial/industrial worker, or construction worker under the exposure
scenarios developed in Step 1. Similarly, off -site surface water and sediment pose no
unacceptable risk for a recreational swimmer, wader, or boater, under the scenarios developed
in Step 1.
Consumption of fish (using on -site surface water data as a surrogate for fish tissue
concentrations) by a recreational fisher and subsistence fisher resulted in hazard indices of
7.2E+00 and 2.1 E+02, respectively. Target endpoint analysis performed indicated hazard
quotients above 1 for cobalt for both a recreational and subsistence fisher. The use of on -site
surface water data to evaluate these potential exposure scenarios likely overestimates risk. This
conservative approach was taken to provide an upper -bound estimate of potential surface water
concentrations. As discussed in Section 4.2.2, modeled surface water concentrations for
COPCs in Lake Norman are lower than their respective criteria (for COPCs that have applicable
water quality criteria) at the edge of the modeled mixing zone. Thus, the potential risks
calculated as part of this assessment need to be considered in this context, as well as
considering the conservative exposure parameters used to evaluate these scenarios.
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Corrective Action Plan Part 2 F)�
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Additional data are needed regarding site -specific conditions including recreational and
subsistence uses (if any) near the site, delineation of source -related and background COls
applicable to the risk assessment, and the evaluation of the exposure parameters and fish
ingestion models used in the risk assessment to qualify these results.
5.4 Step 4: Ecological Risk Assessment
The purpose of a BERA is to: (1) determine whether unacceptable risks are posed to ecological
receptors from chemical stressors, (2) derive constituent concentrations that would not pose
unacceptable risks, and (3) provide the information necessary to make a risk management
decision concerning the practical need and extent of remedial action. The BERA was performed
according to the traditional ecological risk assessment paradigm: Problem Formulation, Analysis
(Exposure and Effects Characterization), and Risk Characterization. Because of the many
permutations of conservative parameters, an Uncertainty Evaluation section was also included.
The BERA generally adhered to the USEPA's "Ecological Risk Assessment Guidance for
Superfund: Process for Designing and Conducting Ecological Risk Assessments" (USEPA
1997) and the "Supplemental Guidance to ERAGS: Region 4, Ecological Risk Assessment"
(USEPA 2015b), as well as NCDENR's "Guidelines for Performing Screening Level Ecological
Risk Assessments" (NCDENR 2003).
Constituents of concern were selected based on factors including the type of source(s),
concentration, background levels, frequency of detection, persistence, bioaccumulation
potential, toxicity/potency, fate and transport (e.g., mobility to groundwater), and potential
biological effects. Screening consisted of comparing the maximum concentration of each
constituent in the applicable media to conservative environmental screening levels. Per Step 3
of the USEPA Region 4 ecological risk assessment guidance, COPCs that were retained using
the risk -based screening were evaluated using a multiple lines -of -evidence approach in the
BERA (USEPA 2015c, 2015d).
Risk characterization involved a quantitative estimation of risk followed by a description and/or
interpretation of the meaning of this risk. The purpose of the risk characterization was to
estimate potential hazards associated with potential exposures to COPCs and their significance.
During risk estimation, the exposure assessment and effects assessment were integrated to
evaluate the likelihood of adverse effects to wildlife receptors of interest (e.g., birds and
mammals). The risk estimate was calculated by dividing the dose estimate from the exposure
assessment by the applicable toxicity reference value (derived from the available literature) to
obtain a hazard quotient.
Receptors chosen for ecological risk assessment are often surrogates for the broad range of
potential ecological receptors in a given habitat. For MSS, typical receptors were chosen for
their expected common presence in the habitats represented at the site, or because they are
common in the southeast and toxicity data are available. Aquatic receptors include fish, benthic
invertebrates, aquatic birds (represented by mallard duck and great blue heron), and aquatic
mammals (represented by muskrat and river otter).
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Corrective Action Plan Part 2 F)�
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At MSS, two ecological exposure areas were defined (Figure 2-5 in Appendix F). These
include:
• Ecological Exposure Area 1, located between the active ash basin and Lake Norman;
and
• Ecological Exposure Area 2, located in the northwest area of the MSS site and adjacent
to the PV structural fill.
Potentially affected areas on -site were classified as aquatic and were evaluated for exposure to
site COPCs. Ecological habitats are presented on Figure 2-6 in Appendix F.
Evaluation of surface water and sediment in the unnamed tributary, AOW water, and AOW
sediment in Ecological Exposure Area 1 indicates a HQ of greater than 1 for a great blue
heron's exposure to selenium and vanadium, at 3 and 22, respectively, using the NOAEL-based
HQs; using the LOAEL-based HQs, the heron's exposure is reduced to 1 for selenium and 11
for vanadium. All other aquatic receptors have chemical HQs below 1. Evaluation of surface
water in Ecological Exposure Area 2 indicates that all aquatic receptors have HQs below 1; the
metal COPCs pose no unacceptable hazards to these receptors in these scenarios.
A heron rookery and an active bald eagle nest are present on -site. Although bald eagles have
been delisted at the federal and county level, they are still listed as a threatened species in
North Carolina. Because the potential exists for this threatened species to inhabit/use the site,
NOAEL-based HQs were used to evaluate potential hazard to this protected receptor. Since the
eagle's diet is partially composed of fish, there may be a concern as the HQs for selenium and
vanadium for the great blue heron, which subsists solely on fish, are 3 and 22, respectively. The
body weight of the eagle is, however, two times greater than the heron. Additionally, the
normalized fish ingestion rate is lower for the eagle than the heron (0.1 mg/kg/day vs. 0.18
mg/kg/day, respectively). Although the anticipated body burden of these COPCs would be at
least two times lower than the great blue heron, additional evaluation is needed to determine
what the potential risk from selenium and vanadium may be to the eagle, as sensitivity can be
both species and constituent -specific.
Additional data and further refined assessment are needed to address uncertainties associated
with the evaluation of these scenarios including the occurrence of these ecological receptors in
the areas adjacent to the ash basins, delineation of source -related and background COls
applicable to the risk assessment, and refinement of the exposure and toxicity assumptions
used in the ecological risk characterization.
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Corrective Action Plan Part 2 F)�
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6 Alternative Methods for Achieving
Restoration
This section discusses how remedial alternatives were evaluated and identifies the remedial
alternative selected to achieve restoration of groundwater quality at the MSS site.
As described in Section 1, this CAP considers cap -in -place as the source control measure for
the ash basin. An engineered cap will minimize infiltration through the covered area, thereby
reducing the contact of infiltrating water with potentially impacted soil. Based on the foregoing,
remediation of soils is not discussed in this document; rather, this CAP focuses on remediation
of groundwater impacts associated with the MSS ash basin system.
As noted in Section 2, exceedances of 2L Standards were measured in groundwater monitoring
wells located between the ash basin and Lake Norman and an unnamed tributary that flows to
the lake. In addition, exceedances of 2B Standards were measured in the surface water
samples collected from the unnamed tributary located east of the ash basin and the dry ash
landfill (Phase 1). It is likely that the primary source of water discharging to the unnamed
tributary is water flowing from within and beneath the southeast portion of the ash basin.
Dewatering of the ash basin will likely decrease the amount of discharge as well as the
concentrations of COls that appear to be discharging to the unnamed tributary. Monitoring of the
unnamed tributary will continue throughout source control activities and further assessment will
be conducted to evaluate a potential groundwater cutoff wall in this specific area of the site, as
described in the sections below.
6.1 Corrective Action Decision Process
6.1.1 Evaluation Criteria
The goal of groundwater corrective action in accordance with 15A NCAC 2L .0106 is:
"... where groundwater quality has been degraded, the goal of any required corrective
action shall be restoration to the level of the standards, or as closely thereto as is
economically and technologically feasible"...using best available technology 0), or to
an alternate standard (k) or using natural attenuation mechanisms (1).
The evaluation of best available methods for groundwater remediation is based on the objective
of meeting groundwater standards at the Compliance Boundary with consideration of
implementability, time, and cost. The methods may include one or a combination of best
available technologies and natural attenuation processes. Source control measures (such as
cap -in -place, excavation, or partial excavation/cap-in-place) are being addressed separately.
The groundwater remedial alternatives herein are evaluated to supplement the selected source
control measure.
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Corrective Action Plan Part 2 F)�
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6.1.2 COls Requiring Corrective Action
Data from the CSA were evaluated in CAP Part 1 to identify the following groundwater COls that
are considered for current or potential corrective action: antimony, arsenic, barium, beryllium,
boron, chloride, chromium, cobalt, hexavalent chromium, iron, manganese, selenium, sulfate,
thallium, TDS, and vanadium. These COls are considered for corrective action because they
have either exceeded their applicable 2L Standard, IMAC, or NCDHHS HSL, or may exceed
them in the future (based on groundwater modeling predictive scenarios) due to fluctuations of
COI concentrations as a result of closure activities.
Variability in detections and concentrations of COls from Round 1 and Round 2 sampling events
were previously discussed in Section 2.3.2. Based on this variability, additional sampling and
data evaluation is recommended to confirm the magnitude and extent of COI exceedances and
so that the most appropriate corrective action(s) for specific COls is selected.
6.1.3 Potential Exposure Routes and Receptors
The Baseline Human Health and Ecological Risk Assessment (Appendix F) provides a
conservative assessment of potential risk associated with the COls attributed to the source
areas at the MSS site.
The primary source -to -receptor exposure route is leaching of ash porewater to groundwater,
which will discharge to Lake Norman and the unnamed tributary flowing to Lake Norman. A
secondary source -to -receptor exposure route may be infiltration of COls in water and/or
sediment from AOWs to groundwater.
At the MSS site, there are no water supply wells downgradient between the source areas and
Lake Norman. Lake Norman is a hydrologic boundary between the ash basin and properties to
the southeast of Lake Norman and Duke Energy property; therefore, consideration of future
water supply wells as receptors downgradient of the source areas does not warrant further
assessment.
Localized groundwater mounding associated with the current hydraulic head in the basin will be
reduced as source control is implemented. After dewatering of the basin and source control, the
groundwater model predicts that the water table elevation in the source areas will be lowered.
These corrective actions have the potential to reduce or eliminate the flow in AOWs associated
with the ash basin and the amount of discharge and concentrations of COls discharging to the
unnamed tributary east of the ash basin, potentially eliminating the exposure pathway to surface
water.
6.2 Alternative Evaluation Criteria
Alternative evaluation criteria are chosen in general conformance with USEPA Office of Solid
Waste and Emergency Response Directive 9355.-27FS, "A Guide to Selecting Superfund
Remedial Actions" (USEPA 1990). This document provides threshold, balancing, and modifying
criteria for selection of a remedy.
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Corrective Action Plan Part 2 F)�
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Potential groundwater corrective action alternatives will be evaluated against the following
criteria:
• Effectiveness (Section 6.2.1)
• Implementability/Feasibility (Section 6.2.2)
• Environmental Sustainability (Section 6.2.3)
• Cost (Section 6.2.4)
• Stakeholder Input (Section 6.2.5)
6.2.1 Effectiveness
Effectiveness is a comparison of the likely performance of applicable technologies while taking
into consideration the following:
1. The estimated area and volumes of media to be treated.
2. Demonstrated reliability to achieve constituent remedial goals under site conditions.
3. Demonstrated reliability to reduce potential risk to human health and the environment in
a timely manner.
Specific effectiveness criteria include:
• Has the potential remedial alternative been demonstrated to be effective at similar sites?
• Does the remedial technology involve treatment that will permanently destroy target
constituents?
• Does the remedial technology involve treatment that will permanently detoxify target
constituents?
• Does the remedial technology involve treatment that will permanently reduce the mobility
of target constituents?
• Will the remedial alternative permanently remove contaminants from the site?
• Can the effectiveness of a potential remedial technology be monitored, measured, and
validated?
• Will a remedial technology reduce potential risk to human health when fully
implemented?
• Will a remedial technology reduce potential risk to the environment when fully
implemented?
• Will a remedial technology be protective of human health?
Technologies that are deemed to be less effective under site -specific conditions than otherwise
comparable technologies will be eliminated on the basis of effectiveness.
6.2.2 Implementability/Feasibility
The screening criteria of implementability evaluates whether implementation of a technology is
technically and administratively feasible. Specific implementability criteria include:
• Are the material resources and manpower readily available to fully implement the
remedial technology in a timely manner?
• Does the remedial technology require highly specialized resources and/or equipment?
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Corrective Action Plan Part 2 F)�
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• Is there sufficient on -site and off -site area to fully implement the remedy?
• Does the remedial technology require any permits, and can the permits be acquired in a
timely manner (e.g., wetlands permitting)?
• Can the remedial alternative be implemented safely?
• Can existing and future infrastructure support the remedial alternative?
• Will a remedial technology increase potential risk to public safety during implementation?
• Will a remedial technology increase potential risk to the environment during
implementation?
• Can a remedial technology meet all applicable or relevant and appropriate requirements
(ARARs)?
Technologies that are deemed impractical under site -specific conditions will be eliminated on
the basis of implementablity/feasibility.
6.2.3 Environmental Sustainability
A remedy is environmentally sustainable when it maximizes short-term and long-term protection
of human health and the environment through the judicious use of limited resources. Metrics
used to measure environmental sustainability include:
• Will constituents be treated to reduce toxicity or mobility, or will treatment transfer the
constituent from one media to another (e.g., discharge constituents in extracted
groundwater to surface water)?
• Is the carbon footprint (energy consumption) of otherwise comparable remedial
alternatives significantly different?
• Will source materials used in the remediation process be recycled or reclaimed?
• Will waste materials generated during the remediation process be recycled or
reclaimed?
• Will renewable sources of energy be used during the remediation process?
• Will natural habitat restoration, enhancement, or replacement be integral to the remedy?
Duke Energy considers environmental sustainability in its alternative evaluation criteria and
where appropriate will incorporate "green" remedial strategies in their evaluation. Green
remedial strategies consider all environmental effects of remedy implementation and
incorporate options to maximize new environmental benefit of cleanup operations (USEPA
2008). Green remediation reduces the demand placed on the environment during remedial
operations to avoid collateral damage to the environment. Green remediation strategies
minimize adverse impacts to other environmental media such as:
• Air pollution caused by emission of carbon dioxide, nitrous oxide, methane, and other
greenhouse gases emitted during remediation.
• Imbalance to the local and regional hydrologic regimes.
• Soil erosion and nutrient depletion causing changes to soil geochemistry.
• Ecological diversity and population reductions.
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Corrective Action Plan Part 2 F)�
Marshall Steam Station Ash Basin
6.2.4 Cost
The criteria of cost will include estimated capital cost and labor that will be incurred during
remedial design and implementation as well as operation and maintenance cost over a 30-year
period. Cost will not be the sole or primary basis for selecting a technology or remedial
alternative; however, cost will be considered when selecting between two or more remedial
technologies or alternatives that are otherwise comparable.
6.2.5 Stakeholder Input
Appropriate stakeholders will be notified pursuant to 15A NCAC 02L .0114.
6.3 Remedial Alternatives to Achieve Regulatory Standards
Source control is the primary corrective action for groundwater restoration at the MSS site and
may include capping in place. Source control options are being evaluated and designed outside
of this CAP; however, source control and active/passive groundwater remediation are
intertwined and should be considered together when evaluating remedial alternatives.
Corrective action alternatives to restore groundwater to 2L Standards in conjunction with source
control measures are discussed below.
6.3.1 Groundwater Remediation Alternatives
Remedial alternatives for restoration of groundwater in accordance with T15A NCAC 2L .0106
include the following:
Source Control, which can include:
o Placement of engineered cap to prevent minimize infiltration and reduce
subsequent COI leaching into groundwater;
o Slurry walls or grout curtains to prevent groundwater interaction with source
material; and/or,
o In -situ solidification/stabilization to reduce or eliminate leaching of COls into
groundwater by mixing soil beneath source areas with pozzolanic materials (i.e.,
Portland cement or bentonite).
Monitored Natural Attenuation — Dilution from recharge to shallow groundwater, mineral
precipitation, and COI sorption will occur over time, thus reducing COI concentrations
through attenuation. Regular monitoring of select groundwater monitoring wells for
specific parameters would be conducted to ensure COI concentrations in groundwater
are decreasing.
• Enhanced Recharge/Flushing — Short-term temporary methods or a permanent
installation for COls that persist. Short-term approaches may include surface irrigation,
infiltration galleries, or ponds/wetlands with permeable bottoms. For long-term
applications, infiltration galleries are needed.
• Enhanced Attenuation, which can include:
o Addition of materials with high sorptive capacity to the saturated zone to reduce
COI levels in groundwater; and
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o Adjusting the pH and/or redox state to enhance precipitation of iron and
manganese oxide/hydroxide minerals to reduce COI levels in groundwater.
Permeable reactive barriers — Trenching and placement of selected material in the
trench that would chemically bond with the COls and reduce their concentrations in
groundwater.
• Water Treatment — Active in -situ groundwater remediation by injection of chemical
and/or air sparging, groundwater extraction and treatment, or passive groundwater
remediation through wetland construction.
A detailed description of remedial alternatives is included in Appendix G.
6.3.2 Monitored Natural Attenuation Applicability to Site
MNA is a strong candidate for corrective action for groundwater impacts identified at the MSS
site. MNA is a strategy and set of procedures used to demonstrate that physiochemical and/or
biological processes in an aquifer will reduce concentrations of COls to levels below regulatory
criteria. The mechanisms that regulate their release from solids and movement through an
aquifer are, for the most part, the same processes that provide chemical controls on movement
of CCR leachate in an aquifer. These processes attenuate the concentration of inorganics in
groundwater by depositing inorganics on aquifer solids removing constituents from groundwater.
An MNA Tier I and Tier II evaluation was conducted for the MSS site by Geochemical, LLC and
is included in Appendix H. The following is a summary of the Tier I and Tier 11 evaluations.
The Tier I analysis used two lines of evidence for attenuation, including: 1) solid -water pair
comparison of COI concentrations was performed, and a mutually rising relationship indicated
attenuation (USEPA 2007a); and 2) laboratory determination of the solid -water partitioning
coefficient, or Kd value (USEPA 1999), was used as a measure of the susceptibility of COls to
sorb to solids and be attenuated. The Tier I analysis indicated that arsenic, barium, beryllium,
boron, chromium, cobalt, lead, thallium, and vanadium are attenuating in groundwater at the
MSS site.
The Tier II demonstration was then performed based on the conceptual model for COI
attenuation involving reversible and irreversible interaction with clay minerals, metal oxides, and
organic matter. Findings from the Tier II demonstration include the following:
• The samples evaluated for Kd determinations were representative of site -specific
conditions.
• Clay minerals and Fe-Mn-AI oxides were found in all samples. Organic matter is likely
not a significant sink for COls at the MSS site.
• Chemical extractions indicated that COls were concentrated in soil samples exposed to
groundwater containing higher concentrations of COls, which most likely indicates that
precipitating iron and possibly manganese have removed other COls through
coprecipitation and adsorption, thus validating attenuation is occurring at the site.
• Chemical extractions were used to determine a probable range of Kd values that suggest
attenuation is taking place for arsenic, barium, chromium, and thallium.
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Additional data collection is necessary to complete the Tier II analysis and then conduct a Tier
III analysis to evaluate specific attenuation mechanisms for each COI, and quantification of the
magnitude of attenuation by specific media to support numerical modeling. The Tier III objective
is to eliminate sites where site data and analysis show that there is insufficient capacity in the
aquifer to attenuate the contaminant mass to groundwater concentrations that meet regulatory
objectives or that the stability of the immobilized contaminant is insufficient to prevent
remobilization due to future changes in ground -water chemistry. The Tier III assessment will be
performed in general accordance with USEPA's "Monitored Natural Attenuation of Inorganic
Contaminants in Ground Water - Volume 2 Assessment for Non -Radionuclides Including
Arsenic, Cadmium, Chromium, Copper, Lead, Nickel, Nitrate, Perchlorate, and Selenium"
(USEPA 2007b).
6.3.3 Site -Specific Alternatives Analysis
Source control is the primary corrective action for groundwater restoration at the MSS site.
Source control for the ash basin could include construction of an engineered cap system (i.e.,
cap -in -place), but will be modified as required based on the final risk ranking classification
proposed by NCDEQ and approved by the CAMC.
Additional remedial technologies were reviewed to develop site -specific alternatives for
addressing groundwater impacts and are detailed in Appendix G. Six remedial alternatives
were evaluated for the MSS site to enhance or supplement source control activities. Provided
below are summaries of each technology's applicability to the site.
1. No further action — This alternative is provided to establish a baseline for comparison to
other alternatives. There would be no remedial actions conducted at the site to remove
the source of COls other than capping -in -place and no further remedial action would be
taken for groundwater. This measure does not include long-term monitoring or
institutional controls.
2. MNA — Attenuation will occur over time due to natural processes, and its extent and
progress will be monitored at appropriate locations in the source area and between the
source and the Compliance Boundary. Water quality will improve over time once the
source area is controlled/capped and as recharge flushes non -impacted water through
the aquifer. Groundwater monitoring would be continued until remedial objectives are
met (i.e., groundwater concentrations are at or below applicable standards or criteria).
Implementing land use controls downgradient of the ash basin will ensure future
potential receptors will not be affected and controls would remain in place until remedial
objectives are achieved.
Adsorption to iron oxides and hydroxides is demonstrated for antimony, arsenic, boron,
barium, cadmium, cobalt, chromium, iron(II), mercury, manganese, nickel, lead,
selenium, sulfate, vanadium and zinc (Dzombak and Morel, 1990). Soil chemistry results
at the MSS site show abundant Fe2O3 and other hydroxides in soils at the site (CSA
Report Table 6-2), and a strong potential for adsorption. A Tier II demonstration based
on that conceptual model was partially completed. Additional data collection is
necessary to complete the Tier II assessment to determine the specific attenuation
mechanisms for each COI and to determine the rate of attenuation such that it may be
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included in groundwater modeling. The groundwater model did not allow for removal of
COI via coprecipitation with iron oxides, which likely resulted in a conservative prediction
of COI transport. Completion of the Tier II tests described in Appendix H will address
this issue. If the completed Tier II analysis indicates a Tier III analysis is warranted, the
additional analysis should be conducted to determine if natural processes are sufficient
to prevent COI exceedances at the groundwater Compliance Boundary.
Based on available assessment results, it is feasible that MNA can be used partially or
entirely to remediate groundwater at the MSS site. It is noted that a groundwater cutoff
wall may be an effective method for addressing impacted groundwater that appears to
be flowing from the ash basin beneath the dry ash landfill (Phase 1) and discharging to
the unnamed tributary that flows to Lake Norman. Further assessment should be
conducted to evaluate the effectiveness of a groundwater cutoff wall in this area of the
site. Two potential options include construction of a slurry wall or emplacement of a
grout curtain.
3. Enhanced Recharge/Flushing with Groundwater Monitoring — It is possible to increase
the rate of groundwater quality improvement by increasing infiltration of uncontaminated
water into portions of a site, thereby flushing, diluting, and attenuating the remnant
concentrations of COls. There are various ways to accomplish this, ranging from short-
term or temporary methods (e.g., surface irrigation using mechanical sprayers) to the
creation of groundwater infiltration galleries or ponds or wetlands with a permeable
bottom, which could be temporary or permanent. Where a continuing source is present,
permanent infiltration galleries may be needed.
The best potential location for enhanced recharge is to the east of the ash basin, where
the dry ash landfill units (Phases I and II) are located. The use of this technology is not
considered appropriate for the MSS site due to the landfill units being located where
enhanced recharge would be most effective.
4. In -situ Sorption or In -situ Chemical Fixation — Various measures can be taken to
enhance attenuation of COls by blending materials that have a high sorptive capacity,
such as clays, peat moss, and zeolites, into the impacted subsurface material.
Contaminated groundwater can also be treated in -situ using chemical fixation to adjust
the pH and/or redox state of the groundwater, which could result in enhancing
precipitation of iron and manganese oxide and hydroxide minerals in the groundwater.
Enhanced formation of these minerals removes iron and manganese from the
groundwater and can effectively co -precipitate and attenuate other COls. Redox
conditions can be adjusted either through addition of one or more reagents or through air
sparging. Bench -scale treatability testing and/or pilot -scale tests are usually required to
verify the effectiveness of this technology at a specific site prior to full-scale application,
and to select the most appropriate reagent and dosage.
Geochemical modeling suggests that iron and manganese are already precipitating
beneath and downgradient of the source areas. Reagent addition (or air sparging) could
encourage the precipitation of COls by changing the redox conditions over targeted
areas and thereby enhancing natural attenuation. In -situ chemical fixation involves the
injection of a chemical oxidant, such as potassium permanganate. Lifetime costs of
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these technologies may be comparable. If these technologies are part of a selected
alternative, it is recommended that both approaches be tested on -site with a pilot -scale
study to evaluate effectiveness of each approach, since a myriad of variables affect their
comparable performance.
Due to the wide distribution of COls in the shallow and deep zones, the application of in -
situ chemical fixation technology would require a very extensive well network to facilitate
application of reagents. It is not feasible to use this technology to manage large land
areas.
It may be feasible to use chemical fixation for the treatment of groundwater east of the
ash basin and dry ash landfill (Phase 1) to prevent the impacted groundwater from
discharging to the unnamed tributary that flows to Lake Norman. This approach could
reduce the flux of COls and therefore reduce loading for MNA treatment. However,
boron is one of the COIs that exceeded groundwater standards at this location, and this
approach has a limited ability to attenuate boron. Application of the technology for this
purpose could be considered in the future following the re-evaluation of site conditions
following completion of source control and potential hydraulic control such as a cutoff
wall.
5. Permeable Reactive Barrier - A permeable reactive barrier (PRB) is a passive form of in -
situ water treatment that removes COls by chemical bonding in the subsurface zone
(ITRC 2005). PRBs are typically constructed by excavating a trench that fully penetrates
the saturated zone of the unconsolidated aquifer and places material that would
chemically bond with the selected COI in the trench to treat the groundwater. The media
that are used for in -situ treatment are selected based on the contaminants required for
removal.
A funnel -and -gate system can also be used to channel the contaminant plume into a
gate that contains the bonding material. The funnels are low -permeability, and the basic
design consists of a single gate with walls extending from both sides. The advantage of
the funnel -and -gate system is that a smaller region can be used to treat the plume,
which can reduce costs. In addition, if the reactive media need to be replaced, it is much
easier to do so because there is less material to replace.
Site -specific media should be evaluated with a range of reactive adsorbents to best
determine the type and blend ratio to effectively remove COls while maintaining
hydraulic conductivity. The PRB lifespan is a function of the COI concentration and the
media removal characteristics. PRBs may be placed as an interim or long-term measure.
If it is anticipated that the COls will continue to persist in groundwater for multiple
decades, long-term remediation may require the periodic replacement of the PRB's
reactive media.
There have been many successful PRB remedies at sites with a wide range of
constituents, but only limited testing with water containing the constituents in ash
leachates (EPRI 2006). Based on a review of data, it appears that the PRB could
comprise a combination of limestone aggregate (to provide PRB stability, transmissivity,
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and pH buffering) and organic materials (mulch, wood chips, etc.) to promote the
reduction of sulfate to sulfide and precipitation of the inorganics, and potentially zero
valent iron to help promote and sustain the reducing conditions. Laboratory tests would
have to be conducted and then scaled to a pilot -scale level to confirm the effectiveness
of PRB materials at the site and whether additives would be necessary to maintain the
required level of permeability.
Considering the size of the MSS site and the uncertainty of effectiveness, installation of
a PRB is not expected to be cost effective or feasible. However, a PRB could potentially
be installed near the unnamed stream east of the ash basin and dry ash landfill (Phase 1)
where the depth to bedrock is relatively shallow, if warranted to treat impacted
groundwater flowing toward the unnamed tributary. However, boron concentrations
exceed the 2L Standard in this location, so pilot -scale tests of the adsorbents shown to
remove boron in the laboratory would be necessary. Site media would need to be
evaluated with a range of adsorbents to determine the optimal blend ratio for effectively
removing COls and maintaining hydraulic conductivity.
6. Groundwater Treatment — As an alternative to in -situ groundwater treatment methods,
groundwater can be removed and treated above ground. Impacted groundwater would
be pumped to the surface (pump -and -treat) or captured at AOWs at the ground surface.
Following treatment, the water may be discharged under an existing NPDES permit or
re -injected underground. Water treatment can be active (requiring the continual addition
of chemicals and typically, electrical power) or passive (systems that take advantage of
reactions that occur in nature, such as constructed wetlands or limestone beds to
provide neutralization).
The use of passive systems is generally restricted to smaller flows because the
approach typically requires much larger land area than active systems, but has the
advantages of less maintenance and lower operating costs. Passive treatment systems,
however, can be ineffective at removing certain COls, such as boron and TDS. Active
treatment systems are generally costly to construct and operate, but can be designed to
effectively lower the concentrations of all COls.
While a zone of depression could be created, thereby minimizing off -site transfer of
COls, it is anticipated that the system would have to operate a considerable time into the
future until groundwater concentrations decrease below applicable standards or criteria.
It may be feasible to evaluate applying this technology in localized portions of the site;
however, the areal extent of the site makes centralized treatment more challenging. A
detailed modeling and pilot study would be needed to predict drawdown and recovery for
system design.
6.3.4 Site -Specific Recommended Approach
As noted in Section 6.3.3, collection of additional groundwater data is needed to establish
trends, better understand background conditions, and identify potential areas requiring
remediation. Based on the limited data to date, observations/approaches are outlined below.
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6.3.4.1 Proposed Areas Evaluated for Remediation
At the MSS site, there are no areas downgradient of the source areas where groundwater has
been reported to exceed applicable 2L Standards, IMACs, or NCDHHS HSLs beyond the ash
basin Compliance Boundary. However, based on the CSA results, it appears groundwater may
be impacted beyond the Compliance Boundary east of the ash basin and dry ash landfill (Phase
1). Surface water samples collected from the unnamed tributary that flows to Lake Norman have
exhibited exceedances of 2B Standards (specifically, ash -related COls sulfate and TDS).
Additional assessment is actively occurring to delineate the extent of groundwater impacts in
this area of the site, specifically to the east/northeast of the unnamed tributary.
If active remediation is deemed necessary in this area of the site, controlling groundwater that
flows from the ash basin beneath the dry ash landfill (Phase 1) toward the unnamed tributary
should be evaluated to supplement MNA. If additional investigations confirm elevated COI
concentrations that cannot be addressed by MNA, alternate corrective actions in the form of
reagent additions or air sparging may be further evaluated in the future.
6.3.4.2 Recommended Corrective Action
As noted in Section 6.3.3., available assessment results indicate it is feasible that MNA can be
used partially or entirely to remediate groundwater at the MSS site in conjunction with source
control by cap -in -place. It is noted that a Tier III MNA analysis is recommended to verify site -
specific conditions are adequate for potential naturally occurring reactions. Existing data
demonstrates MNA is a viable remedial approach, but additional data to assess system capacity
and stability and evaluate the mechanisms of inorganic attenuation is needed to support this
approach.
In addition to MNA, a groundwater cutoff wall may be an effective method for remediating
impacted groundwater that appears to be flowing from the ash basin beneath the dry ash landfill
(Phase 1) and discharging to the unnamed tributary that flows to Lake Norman. Further
assessment should be conducted to evaluate the effectiveness of a groundwater cutoff wall.
Two potential options include construction of a slurry wall or emplacement of a grout curtain.
The implementation cost of MNA for a 30-year period and additional assessment for evaluating
groundwater diversion is estimated to cost $7,030,000. Monitoring to evaluate the effectiveness
of MNA as a corrective action is summarized in Section 9.0. Costs are discussed further in
Section 10.
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7 Selected Corrective Action(s)
Corrective action(s) for the MSS site were selected based on the evaluation of site conditions as
described in previous sections and the evaluation of alternatives described in Section 6. Based
on the remedial alternatives evaluation, MNA was determined to be the most appropriate
corrective action to support source control; however, groundwater quality should be monitored
following implementation of the proposed closure activities to evaluate if MNA remains a viable
corrective action after basin closure. The final closure option selected will be modified as
required based on the final risk classification proposed by NCDEQ and approved by the CAMC.
7.1 Selected Remedial Alternative for Corrective Action
If consistent with the final NCDEQ risk classification, and if ongoing monitoring data support it,
MNA, in conjunction with an engineered cover system as source control, is recommended on
the basis of environmental protection, technical effectiveness, and sustainability. Further
assessment should be conducted to evaluate the effectiveness of a groundwater cutoff wall for
remediating impacted groundwater that appears to be discharging to the unnamed tributary that
flows to Lake Norman.
Subsequent to closure, it is reasonable to assume that COls remaining in groundwater will
decrease in concentration over time as upgradient non -impacted water moves through the
aquifer. Groundwater flow and geochemical modeling indicates that attenuation by a
combination of sorption, chemical precipitation, and dilution by surface water infiltration and
fresh groundwater effectively dissipate COls in groundwater beneath and downgradient of the
source areas. During and following ash basin dewatering and capping, groundwater hydrology
and geochemistry will likely change and monitoring wells located within the cap footprint will be
decommissioned and removed, as needed.
The Tier III MNA analysis will be conducted in conjunction with or shortly after installation of the
additional assessment wells described in Section 8. Groundwater monitoring will also be used
to evaluate changes in hydrology and geochemistry and refine geochemical and groundwater
modeling predictions presented in Section 4. A monitoring plan is discussed in detail in Section
9 of this report.
7.2 Conceptual Design
7.2.1 Source Control — Cap -in -Place
This proposed CAP considers cap -in -place as the source control measure for the ash basin. An
engineered cap will reduce infiltration through the covered area, thereby reducing the potential
of leaching of COls into the groundwater underlying the closed basin. Note that the final closure
option selected will be modified as required based on the final risk classification proposed by
NCDEQ and approved by the CAMC.
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7.2.2 MNA
7.2.2.1 Demonstration of MNA
The use of MNA as a corrective action involves monitoring select parameters to determine if COls
are attenuating as a result of the corrective action. Once the ash within the ash basin is capped, it
is anticipated that groundwater quality will improve over time due to the attenuation of COls from
the recharge of non -impacted groundwater, precipitation, and adsorption of Cols.
Tier I and 11 analyses were conducted for the MSS site (discussed in Section 6.3.2 and presented
in Appendix H). A geochemical site conceptual model for COI attenuation involving interaction
with site samples containing clay minerals, metal oxides, and organic matter was completed. The
most significant finding was that the precipitation of iron and manganese serves to remove other
COls through co -precipitation and adsorption, thus confirming that attenuation is occurring. In
support of this reaction, clay minerals and Fe-Mn-AI oxides were found in samples.
Evaluation of geochemical modeling indicated COls are attenuated by a combination of sorption
and/or precipitation. TDS and sulfate generally are not attenuated, but concentrations are reduced
by diffusion, mechanical mixing, and/or dilution. Arsenic and chromium were calculated to have
limited solubility; therefore, these constituents do not migrate readily in groundwater. Groundwater
fate and transport model predictions presented in Appendix B are supported by the findings of
the geochemical modeling presented in Appendix E. Based on review of the groundwater
modeling results, COls with sorption coefficients similar to or greater than arsenic are immobilized
by sorption and/or precipitation, but COls with sorption coefficients similar to or less than boron
are not readily attenuated by sorption to solid site materials and are more readily transported by
groundwater moving through impacted media.
Groundwater modeling did not take into consideration the removal of COls via co -precipitation
with iron oxides, which likely resulted in an over -prediction of COI transport, causing some of the
COIs to exceed the 2L Standards at the Compliance Boundary in the model output. Surface water
and groundwater interaction modeling has determined that, even with over -prediction of COls to
Lake Norman, exceedances of 2B Standards are not predicted to occur.
7.2.2.2 Verification of MNA
The MNA monitoring program, data collection, and evaluation to advance the Tier III assessment
should be implemented prior to any cap -in -place activities. If the results of the Tier III assessment
support the use of MNA, effectiveness monitoring should be continued until water quality meets
remedial objectives (e.g., applicable regulatory standards or PPBCs, as applicable). The site
monitoring requirements are discussed in Section 9.
If the number of COls or COI concentrations are determined to be increasing over time during
MNA monitoring, the effectiveness of MNA will be re-evaluated and additional remedial
alternatives will be considered. If warranted, additional corrective actions will be implemented.
Due to the changes in groundwater hydrology and geochemistry that are anticipated to occur as a
result of proposed closure activities, interim monitoring activities are recommended along with the
proposed corrective action, as outlined in Section 8. Monitoring plans to evaluate the
effectiveness of MNA are detailed in Section 9, and the implementation schedule is presented in
Section 10.
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8 Recommended Interim Activities
Interim activities are proposed at the MSS site to address additional information needs identified
in the CSA and CAP Part 1 reports and to refine geochemical and groundwater model
predictions. These activities include the installation of additional monitoring wells and
groundwater sampling during closure activities.
8.1 Additional Monitoring Well Installation
Approximately 13 additional monitoring wells are currently being installed to address additional
information needs identified in the CSA Report and during post-CSA review comment meetings
with NCDEQ. The additional wells will be used to further refine the horizontal and vertical extent
of groundwater impacts, refine the understanding of groundwater flow direction, refine
geochemical and groundwater modeling predictions, and provide additional background
monitoring locations. Locations of the proposed additional assessment monitoring wells are
shown on Figure 8-1.
The additional monitoring wells will be incorporated into the groundwater monitoring network in
2016 and sampled in conjunction with the existing monitoring wells, as described in Section 9.
8.2 Additional Groundwater Sampling and Analyses
Additional sampling of select monitoring wells will be conducted at the MSS site during 2016.
The number of qualifying sampling events and locations (i.e., where turbidity was less than 10
NTU) of background wells have been limited such that PPBCs presented in the CAP Part 1
report for select constituents could not be statistically derived. Groundwater sampling results
from proposed First and Second Quarter 2016 sampling events, as described in Section 9, will
be used to supplement the existing background well database and support statistical analysis
for calculation of revised PPBCs.
In response to NCDEQ comments to the CSA Report, additional radionuclide sampling will also
be performed in wells along inferred groundwater flow pathways through the ash basin and in
background wells. This sampling will be coordinated to coincide with either the First or Second
Quarter 2016 sampling event.
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Corrective Action Plan Part 2 F)�
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9 Interim and Effectiveness Monitoring Plans
The Interim and Effectiveness Monitoring Plans (Monitoring Plans) provide detailed information
regarding the purpose, schedule, and methods for collection of groundwater, surface water, and
ash basin water samples at MSS. The Monitoring Plans are intended to evaluate the
effectiveness of proposed corrective actions; monitor the movement of contaminants in
groundwater during and after proposed future closure activities (i.e., capping) of the MSS ash
basin system; and provide data for evaluation of baseline conditions and seasonal variation in
groundwater, surface water, and ash basin water at the MSS site. These Monitoring Plans
supersede the monitoring plan provided in the CSA (Section 16 — Interim Monitoring Plan).
Protocols for groundwater, surface water, and ash basin water sample collection, analysis, and
reporting are consistent between the Monitoring Plans. This sampling and analysis will be
completed in general accordance with the Monitoring Plans presented below, the CSA Work
Plan, and the Low Flow Sampling Plan (CSA Report Appendix G).
9.1 Interim Monitoring Plan
The Interim Monitoring Plan has been developed to provide baseline seasonal analytical data
associated with the MSS site. The Interim Monitoring Plan will be implemented through the first
half of 2016. The Interim Monitoring Plan establishes data quality objectives (DQOs) and
sampling requirements associated with sampling frequency, sampling locations, and analytical
requirements. Upon completion of the Second Quarter 2016 sampling event, monitoring
activities will be conducted in accordance with the Effectiveness Monitoring Plan described in
Section 9.2.
9.1.1 Data Quality Objectives
The following DQOs are associated with the Interim Monitoring Plan:
• Monitor the extent of groundwater contamination in and around the MSS site and
evaluate seasonal trends associated with COIs.
• Monitor the movement of COls within groundwater and the interaction with surface
water.
• Determine seasonal groundwater flow direction and elevations, and monitor potential
changes to groundwater flow direction and elevation resulting from seasonal variation.
The DQOs will be met through the following activities:
Perform groundwater, surface water, and ash basin water sampling at the locations
depicted on Figure 2-1 and Table 9-1 through the first half of 2016. These monitoring
events, planned for first and second quarters of 2016, will be combined with analytical
data from CSA rounds 1 through 4 (collected in the second half of 2015) to evaluate
seasonal water quality conditions and background groundwater concentrations at the
MSS site. Additional assessment wells are being installed at the MSS site as of February
2016 and will be added to the Interim Monitoring network following installation.
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Corrective Action Plan Part 2 F)�
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• Perform groundwater static water level measurements at site -wide monitoring wells
concurrent with groundwater sampling described above.
• Perform water level gauging at previously established stream and surface water
locations.
• Perform total depth measurements at site -wide monitoring wells on an annual basis.
• Prepare reports documenting sampling results and analysis for submittal to NCDEQ, as
specified in Section 9.1.3 below.
9.1.2 Sampling Requirements
9.1.2.1 Sample Frequency
To meet the DQOs and evaluate seasonal fluctuations in COI concentrations, sampling of CSA,
compliance, voluntary, and background groundwater monitoring wells and surface water
locations will be conducted at the MSS site in the First and Second Quarters of 2016. Sampling
frequency will be revised as described in the Effectiveness Monitoring Plan (Section 9.2) upon
completion of the Second Quarter 2016 monitoring event.
9.1.2.2 Sample Locations
Groundwater monitoring well, surface water, and ash basin water locations to be sampled
during the Interim Monitoring are identified in Table 9-1 and depicted on Figure 2-1. Monitoring
wells may be added to the sampling program through the installation of additional monitoring
wells (i.e., assessment wells shown on Figure 8-1) or removed as proposed closure activities
lead to well abandonment. NCDEQ will be notified and NCDEQ's approval will be obtained prior
to the abandonment of these monitoring wells.
9.1.2.3 Analytical Requirements
Analytes for monitoring wells, surface water, and ash basin water include total and dissolved
metals, alkalinity (total, bicarbonate, and carbonate), calcium, chloride, hexavalent chromium,
potassium, magnesium, nitrate, sodium, sulfate, total combined radium, total combined uranium,
total dissolved solids, total organic carbon, and total suspended solids. In addition, samples will
be analyzed for ammonia for use in evaluation of MNA as a corrective action. Analytical
services will be provided by a North Carolina certified laboratory. Chemical analytes, analytical
methods, bottle requirements, and preservatives are provided in Table 9-2.
9.1.3 Reporting
Validated analytical results from the First Quarter 2016 monitoring event are proposed to be
transmitted to NCDEQ within 90 days of completion of the sampling event. Within 120 days of
completion of the Second Quarter 2016 monitoring event, Duke Energy proposes to submit a
groundwater monitoring report to NCDEQ that summarizes the results from the First and
Second Quarter 2016 monitoring events.
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9.2 Effectiveness Monitoring Plan
The Effectiveness Monitoring Plan has been developed to monitor select wells for MNA
parameters to provide baseline MNA data prior to basin closure; to monitor potential influence of
closure activities on COIs; and to monitor the effectiveness of MNA as a corrective action
following basin closure. The Effectiveness Monitoring Plan will be implemented using select
wells following completion of the Second Quarter 2016 sampling event and will continue through
2020 (five years of CAP -related sampling). The Effectiveness Monitoring Plan may be modified
within the first five-year period if additional corrective actions are implemented.
9.2.1 Data Quality Objectives
The following DQOs are associated with the Effectiveness Monitoring Plan:
• Monitor the effectiveness of the approved remedies identified for the ash basin system.
• Monitor changes in groundwater and surface water concentrations as the result of
proposed closure activities (i.e., capping) associated with the ash basin system.
• Monitor the movement of COls within groundwater and the interaction with surface
water.
• Collect additional analytical data from background wells to revise PPBCs.
• Monitor seasonal groundwater flow direction and elevations, and monitor potential
changes to groundwater flow direction and elevation resulting from proposed closure
activities.
The DQOs will be met through the following activities:
• Perform groundwater and surface water sampling, including MNA parameters, at select
locations.
• Perform groundwater static water level measurements of select monitoring wells
concurrent with groundwater sampling described above.
• Perform water level gauging at previously established stream and surface water
locations concurrent with sampling events.
• Perform total depth measurements at monitoring wells on an annual basis.
• Prepare reports documenting sampling results and analysis for submittal to NCDEQ.
9.2.2 Sampling Requirements
Following the Second Quarter 2016 monitoring event, four seasonal monitoring events,
including Rounds 1 and 2, will have occurred at the MSS site (Rounds 3 and 4 were background
well only sampling events). Results from the four seasonal monitoring events will be evaluated
to establish an MNA sampling network of select monitoring well and surface water locations.
Additional monitoring of the MNA sampling network will be proposed to confirm the
effectiveness of MNA as a proposed corrective action and to determine if additional sampling is
warranted at locations outside the MNA network to monitor site conditions.
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9.2.2.1 Sample Frequency
Following the establishment of the MNA network, one additional monitoring event of these
locations will be conducted in 2016 in conjunction with the Third 2016 NPDES compliance
sampling event in October. Beginning in 2017, samples from the MNA network will be collected
three times per year, in conjunction with the NPDES compliance monitoring, in order to correlate
the results from the MNA network results with the NPDES sample results. Sampling frequency
associated with Effectiveness Monitoring will be re-evaluated every five years. Upon completion
of the first five-year sampling cycle, the potential for semi-annual sampling frequency will be
evaluated.
In order to revise PPBCs using the additional background wells as described in Section 8, an
additional monitoring event will be conducted in 2016 from all MSS background monitoring wells
in order to obtain four rounds of analytical data in 2016. Based on the sampling schedule
proposed in the Interim Monitoring Plan and the scheduled effectiveness monitoring to be
conducted concurrent with the NPDES compliance monitoring (scheduled for February, June,
and October 2016), it is anticipated this additional background sampling event would be
conducted in the Second Quarter 2016 (i.e., June 2016).
9.2.2.2 Sample Locations
Sampling locations associated with the Effectiveness Monitoring Plan will be established after
collection of the Second Quarter 2016 sampling event, following evaluation of four seasonal
monitoring events. Sample locations will be proposed to NCDEQ prior to implementation of the
Effectiveness Monitoring Plan.
9.2.2.3 Analytical Requirements
Samples collected from the MNA network will be analyzed for the parameters described in the
Interim Monitoring Plan above (Section 9.1 and Table 9-2). Changes to the analytical
requirements may be proposed upon evaluation of the seasonal monitoring results obtained
during CSA and interim monitoring.
9.2.3 Reporting
Monitoring reports analyzing the results from the each monitoring event are proposed to be
submitted to NCDEQ within 120 days of completion of each sampling event. Results from the
additional background monitoring event will be included in the next scheduled monitoring report.
9.3 Sampling and Analysis
9.3.1 Monitoring Well Measurements and Inspection
Groundwater sampling will be conducted at monitoring well locations associated with the CSA,
compliance, voluntary, and additional assessment wells as described in the Monitoring Plans
above.
During each monitoring event, monitoring wells will be measured for static water levels. These
measurements will be taken within one 24-hour period and prior to sampling to minimize
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temporal variations. The depth to water measurements, along with date and time, will be
recorded on a dedicated field form, a field notebook, and/or electronically via the iForms
software program or comparable system.
Monitoring wells will be measured for total depth during the Second Quarter 2016 sampling
event and during the first sampling event in subsequent years. Measurements will be recorded
on a dedicated field form, a field notebook, and/or electronically via the iForms software
program or comparable.
The thickness of sediment accumulated in each monitoring well will be calculated once each
year, during the second sampling event of the year. Sediment thickness will be calculated by
comparing current total depth with historical data. If more than one foot of sediment exists, wells
will be redeveloped with a pump or bailer prior to the third sampling event. In addition, wells may
be redeveloped if turbidity readings below 10 NTU cannot be achieved during sample purging.
Wells where turbidity less than 10 NTU cannot be obtained may still be sampled in accordance
with the Low Flow Sampling Plan. Monitoring wells with turbidities greater than 10 NTU after
redevelopment may be considered for replacement.
Each monitoring well will be inspected while performing water level measurements for damage
to the casing, protective casing, and bollards. Well caps and locks will be inspected to
determine whether they are in good working order and functioning properly. Flush -mounted
wells will be inspected for any damage by vehicular traffic and to ensure that the water -tight
gasket is functioning properly.
9.3.2 Surface Water Measurements
Stream stage measurements will be conducted at gauging locations along Lake Norman and
the unnamed tributaries to Lake Norman. Each gauging location will have a designated datum
point from which the relative stream level will be measured.
9.3.3 Sample Collection
9.3.3.1 Monitoring Well Purging
Monitoring wells will be purged and sampled using low -flow (minimal drawdown) methods in
accordance with the Low Flow Sampling Plan. The low -flow technique will be used to determine
when a well has been adequately purged and is ready to sample by monitoring the pH, specific
conductance, temperature, ORP, DO, and turbidity. The volume of water that is removed will
also be observed and recorded. Wells with slow recharge rates, excessive drawdown, or that
require a higher pumping rate may be purged using the volume -averaging method.
An adequate purge is achieved when the pH, specific conductance, ORP, DO and temperature
of groundwater have stabilized and the turbidity is below 10 NTU.
9.3.3.2 Groundwater Sample Collection
After purging and stabilization are accomplished, laboratory -supplied sample containers will be
carefully filled using the same method utilized for purging. Appropriate sample containers,
quantities, and preservatives for the various analyses are listed in Table 9-2.
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9.3.3.3 Surface Water Sample Collection
Grab samples will be collected from each surface water sample location shown on Figure 2-1.
Water quality parameters (pH, specific conductance, ORP, temperature, DO and turbidity) will
be measured at each location. After water quality parameters have been collected and
recorded, surface water samples will be collected by slightly submerging the lip of the sample
container under the water surface, or by using a dip cup sampler in areas with difficult access.
Samples collected for dissolved metals analysis will be field -filtered through a 0.45-micron filter
on the day of collection using a peristaltic pump. Filled laboratory -supplied sample containers
will be labeled and placed in a cooler on ice (4°C) and maintained at that temperature until
delivery to the laboratory.
9.3.3.4 Sample Naming Convention
Samples will be identified by the following convention: site code, sample identification name,
sample matrix, and date code. The codes are further explained below.
• The two -digit Site Code for MSS is MA.
• Sample Identification Name will be the sample location name (i.e., BG-1 D).
• Sample Matrix
o NS — Normal Sample
o FD — Field Duplicate
o EB — Equipment Blank
o AMB — Ambient Blank
o FB — Filter Blank
o TB — Trip Blank
• Date Code is a four -digit code indicating the quarter and year a sample was collected.
For example, a groundwater sample collected from monitoring well BG-1 D in February 2016
would be designated MA-BG-1 D-NS-1 Q16. If a field duplicate was also collected from that
location, it would be designated MA-BG-1 D-FD-1 Q16.
9.3.3.5 Waste Handling
Purge water and decontamination water will be discharged to the ground surface at each
individual sample location unless otherwise directed by Duke Energy. Other investigation -
derived waste, including disposable tubing and gloves, will be handled in accordance with the
MSS site solid waste protocols.
9.3.3.6 Chain of Custody and Sample Delivery
All samples will be tracked using proper chain -of -custody procedures. A separate chain -of -
custody will be filled out by each sample team and accompany each cooler shipped. Samples
will be hand -delivered or shipped to the appropriate contract laboratory.
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9.3.4 Quality Assurance/Quality Control
In addition to laboratory and other quality assurance/quality control procedures, field quality
control measures will be implemented to ensure that data meets project requirements. The
following field quality control procedures will be utilized for this project:
• Field Duplicates — Field duplicate samples will be collected by filling two identical sets of
sample containers with water from the same sample location for each of the planned
analyses. Field duplicates will be given unique sample numbers.
• Equipment Blanks — Equipment blanks measure the cleanliness of field sampling
equipment. Equipment blanks will be created by pouring reagent -grade water over a
decontaminated pump and collecting the water in appropriate sample containers.
Equipment blanks will receive all the tests that are to be performed on the associated
samples.
• Ambient Blanks — Ambient blanks measure background contamination in the field.
Appropriate sample containers will be filled with reagent -grade water while other water
samples are collected at the site.
• Filter Blanks — Filter blanks evaluate the possible addition of chemicals from the filter to
the sample, thus measuring potential contamination in the filters. Filter blanks will be
created by filling the appropriate sample containers with reagent -grade water run
through a new filter.
• Trip Blanks — Trip blanks will be created by the laboratory and accompany low level
mercury samples through sample container shipment and delivery to the site, sample
collection, and delivery back to the laboratory for analysis.
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10 Implementation Cost and Schedule
CAMA Section §1 30A-309.21 1 (b)(1) requires implementation of corrective action within 30 days
of CAP approval. Ash basin closure planning and implementation is ongoing at the MSS site
and compliance groundwater monitoring has been conducted since 2011.
10.1 Implementation Cost
The recommended corrective action to supplement source control at the MSS site (i.e.,
proposed capping based on pending risk classification) is MNA. In addition, further investigation
should be conducted to evaluate the effectiveness of a potential groundwater cutoff wall east of
the ash basin and dry ash landfill (Phase 1). A summary of costs associated with implementation
of the MNA program and evaluation of a groundwater cutoff wall east of the ash basin is
provided in Table 10-1. Note that the actual costs will be highly dependent on the actual
conditions that exist following capping and completion of ash basin closure activities. Therefore,
these values represent an estimate for reference purposes only.
Table 10-1 Estimated Capital and Annual Costs for MNA and Evaluation of Groundwater
Cutoff Wall
Capital Costs — MNA Monitoring Well Installation
Monitoring Well Installation (10 wells)
$180,000
Site Preparation and Erosion and Sediment Control
$30,000
Field Oversight (15%)
$31,500
Well Installation Reporting
$5,000
Project Management (10%)
$24,700
Contingency (20%)
$54,300
Subtotal Monitoring Well Installation
$325,500
Capital Costs — Evaluation of Groundwater Cutoff Wall
Planning Documents/Initial Preparation
$35,000
Sediment and Erosion Control
$15,000
Site Preparation
$11,000
Field Investigation Activities
$40,000
Subtotal Evaluation of Groundwater Cutoff Wall
$101,000
Total Capital Costs
$426,500
Annual Costs - Monitoring/Reporting
Lab Analysis (32 samples)
$19,200
Data Validation
$15,000
Reporting
$60,000
Equipment and Expendables
$9,000
Sampling Labor
$38,400
Project Management (10%)
$14,160
Escalation to Mid -Point (4%)
$6,230
Annual Monitoring/Reporting Costs
$162,000
Total Capital/Annual Costs for Project Duration
$7,030,000
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10.2 Implementation Schedule
Interim activities, including advancement of the MNA Tier III assessment, will continue to be
implemented at MSS until closure activities have been completed.
Groundwater, surface water, ash basin water (pending capping status) and AOW sampling
associated with the Interim Monitoring Plan will be implemented at the MSS site through the
Second Quarter 2016, as detailed in Section 9.1. Following the Second Quarter 2016 sampling
event, an MNA monitoring network of wells will be established and sampled concurrent with the
NPDES compliance monitoring beginning in November 2016. Monitoring will be conducted three
times per year in accordance with the Effectiveness Monitoring Plan described in Section 9.2
and coincide with NPDES compliance sampling events scheduled annually in February, June,
and October.
MNA will continue to be evaluated after closure activities are completed and subsurface
conditions have stabilized. Should these results indicate that MNA is effectively reducing COI
concentrations in groundwater, monitoring will continue per the Effectiveness Monitoring Plan.
Based on the monitoring data, recommendations will be made regarding modifications in the
monitoring program, changes in the implementation of the selected remedy, or if other
alternatives need to be considered.
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