HomeMy WebLinkAboutNC0001422_CSA Appx C - Methodology 2015-07-31_20150805Duke Energy Progress – L.V. Sutton Energy Complex
Groundwater Assessment Report
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Appendix C - Methodology
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The approach to conducting the Comprehensive Site Assessment (CSA) at the L.V. Sutton
Energy Complex was described in the Groundwater Assessment Work Plan (Revision 1, December
2014). The objective was to collect and analyze samples of soil, ash, groundwater, surface
water, and sediment to more accurately determine the vertical and horizontal concentrations of
Constituents of Interest (COIs). A COI is defined as a parameter detected at a concentration
greater than NCDENR/DWR Title 15, Subchapter 2L and Interim Maximum Allowable
Concentrations (IMAC). This section describes equipment used and methods employed to
collect and preserve appropriate samples and obtain representative analytical results.
1. Subsurface Investigation
Characterization of subsurface material was conducted by collecting ash, soil, sediment, ash
pore water, groundwater, and surface water samples for analysis. Ash, soil, ash pore water,
and groundwater samples were obtained through completion of drilled borings and monitoring
wells. The following presents the approach for subsurface sample acquisition and analysis.
1.1 Drilling Methods
Sonic drilling methods were employed to collect subsurface samples. The advantages
provided by this method include less disturbance of the borehole wall and minimized
groundwater sample turbidity. Drilling tools (sonic core barrels and casings) were
thoroughly decontaminated prior to starting a boring. Daily equipment rinse samples
were collected to confirm the effectiveness of decontamination. Drinking water
purchased locally was used for drilling fluid. A sample of the “source water” was
analyzed for the full set of GAP parameters (Attachment 4).
1.2 Monitoring Well Installation
Each monitoring well was constructed by North Carolina-licensed well drillers using
sonic drilling techniques and in accordance with 15A NCAC 02C (Well Construction
Standards). Drilling equipment was decontaminated prior to use at each location.
Monitoring wells were constructed of 2-inch ID, National Sanitation Foundation (NSF)
grade polyvinyl chloride (PVC) (ASTM D-1785-12) schedule 40 flush-joint threaded
casing and 0.010-inch machine-slotted pre-packed screens. Well construction also
included the use of pre-packed screens with additional sand in the annular space, to
minimize sample turbidity. Packed well screens for each well were filled with clean,
well-rounded, washed high grade No. 1A silica sand. The filter pack was placed
approximately two feet above the top of the pre-packed screen and then an approximate
two-foot pelletized bentonite seal was placed above the filter pack. The remainder of the
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annular space was filled with a neat cement grout from the top of the upper bentonite
seal to near ground surface.
ABMW-2D was installed as double-cased well beneath the ash in the FADA. Protective
outer casing was installed using sonic drilling equipment with a 10-inch core barrel
below the base of the ash in the underlying surficial formation, which was determined
based on observation of continuous cores recovered during drilling. A permanent 6-
inch diameter schedule 40 PVC protective outer casing was then installed and grouted in
place. After the grout had sufficient time to set (approximately 24 hours), drilling was
advanced through the outer casing using a smaller diameter drilling core barrel (~5-inch
diameter) and through the surficial aquifer to the top of the Pee Dee formation
(determined based on observation of continuous cores) at least 10 feet below the depth
of the surface casing. The well was then installed in a similar approach as shallow
monitoring wells as described above.
Monitoring wells were completed with either steel above ground protective casings or
flush mounts (SMW-01) with locking caps, locking expansion caps, and well tags.
Protective covers were secured and completed in a concrete collar and a minimum two-
foot square concrete pad surrounded by bollards.
1.2.1 Monitoring Well Development
Following installation, monitoring wells were developed to remove drill fluids,
clay, silt, sand, and other fines which may have been introduced into the
formation or sand pack during drilling and well installation, in addition to
establishing connectivity of the well with the aquifer. Well development was
performed using a portable submersible pump that was repeatedly moved up
and down the well screen interval until the water was relatively clear. Some
wells were initially developed with a bailer to remove the most turbid water and
were later completed by developing with a submersible pump or a peristaltic
pump. Development continued by sustained pumping until monitoring
parameters (e.g., conductivity, pH, DO, and temperature) were generally
stabilized, estimated quantities of drilling fluids, if used, were removed, and
turbidity decreased to acceptable levels (approximately 10 NTUs). Wells were
developed no sooner than 24 hours after well installation to allow for an
adequate grout cure time.
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1.3 Sample Collection and Analytical Methods
Methods used for the collection and preservation of samples for various analyses are
described in this section. Samples were collected in accordance with the quality
assurance and quality control procedures outlined in the Work Plan.
1.3.1 Soils and Ash Sampling and Analysis
Borings were logged and ash/soil samples were photographed, described, and
visually classified in the field for origin, consistency/relative density, color, and
soil type in accordance with the Unified Soil Classification System (ASTM
D2487/D2488).
Rinse blanks from soil sample collection equipment were collected for each soil
boring/well installation location. At times, drilling for one location took more
than one day and the rinse blank was collected on the first day. Rinse blanks for
soil samples were collected by pouring deionized water through the sonic drill
bit or through the hand auger bit. These pieces of equipment are normally the
first introduced into the subsurface for a soil boring. Laboratory results for the
rinse blanks are provided in Appendix D.
Soil and ash samples were collected wearing nitrile gloves and prepared and
analyzed using the following methods:
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1.3.1.1 Metals
Soil and ash samples were placed in amber glass bottles and stored on ice
for shipment for total metals analysis. Concentrations of metals present
in soils and ash were determined using analytical parameters presented
on Table 6-2.
1.3.1.2 Organic Constituents
Soil and ash samples were placed in amber glass bottles and stored on ice
for shipment for total organic carbon (TOC) analysis. TOC content of
soils and ash were determined in accordance with EPA Method 9060.
1.3.1.3 Leaching Characteristics
Select soil and ash samples were placed in amber glass bottles and stored
on ice for shipment forthe mobility of inorganic analytes present using
the Synthetic Precipitation Leaching Procedure (SPLP) following U.S.
EPA Method 1312.
1.3.1.4 Bulk Chemistry
Select soil and ash samples were stored and shipped in sealable plastic
bags for bulk chemistry analysis. Identification and relative
concentration of bulk chemistry was determined by American Assay
Laboratories. Samples were dried at 80 oC overnight and pulverized to -
150 mesh and analyzed as follows:
XRF-PP – a known sample amount was combined with binder,
ground finer, and pressed into a disk. The disk was then analyzed
by X-ray fluorescence (XRF).
ICP-D4A – A sample pulp was digested with a combination of HF,
HClO4, HCl, and HNO3 for a near-total digestion. The solution
was then analyzed by Inductively Coupled Plasma (ICP)-Atomic
Emission Spectroscopy (AES) and ICP-Mass Spectroscopy (MS).
ICP-NF – A sample pulp was fused with Na2O2 and digested with
HCl. The solution was then analyzed by ICP-AES and ICP-MS.
Eltra Carbon & Sulfur – A sample pulp was combined with
tungsten and iron accelerator and combusted in Eltra furnace for
analysis of carbon and sulfur.
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Loss of Ignition (LOI) – A sample pulp was gradually heated in a
gravimetric furnace to 1000° C while sample loss was calculated.
1.3.1.5 Mineralogy
Select samples were stored and shipped in sealable plastic bags for
mineralogical analysis. Identification and relative concentration of
mineral types were determined by X-ray diffraction (XRD). The original
sample was dried at 80° C (no pulp) and combined with water and
disaggregated in an ultrasonic bath. The sample was then wet sieved at
63 micrometers to separate and quantify the sand fraction. The slurry
was centrifuged at a calculated rotation per minute and time to separate
the clay particles from the silt. The clay solution was then decanted off.
Sand and silt fractions were dried, quantified, and analyzed using XRD as
random mounts (XRD is a process by which X-rays are scattered by atoms
that comprise the crystal structure of a given mineral, creating a pattern).
Clay particles are deposited on slides forming an oriented mount for
XRD. After the analysis, the clay particles were placed in an ethylene
glycol environment overnight to test for expanding clays. When
necessary, the clay particles are then heated to 400° C and re-analyzed for
collapsing layers.
1.3.1.6 Development of Kd Terms
To determine the sorption capacity of site soils, select samples were
collected along proposed flowpath transects. Samples were collected,
handled, and preserved in order to eliminate impacts of ambient air on
the oxidation-reduction potential (ORP) and hydrous ferrous oxide
(HFO) on sampled materials. Samples were collected in plastics bags and
sealed with a conventional vacuum sealer. The samples were stored on
ice for shipment and kept out of direct sunlight.
Samples were prepared and analyzed by the Civil and Environmental
Engineering Department of the University of North Carolina at Charlotte
(UNCC). Prior to sorption determinations, soil samples were dried at
room temperature and periodically mixed throughout the drying process
to prevent grain aggregation. Once dry, samples were sieved using a No.
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10 U.S. standard sieve (10 mm) with 0.0787 inch openings. To quantify
soil partition coefficients (Kd), column and batch tests were performed.
Effluent samples collected from these tests were analyzed by inductively
coupled plasma-mass spectroscopy and ion chromatography. To provide
a basis for estimating COI source terms, leaching tests were performed on
ash samples. Details of the analytical procedures/methods are briefly
discussed below with more detail included in the analytical reports.
1.3.1.6.1 Column Tests
Column tests were conducted by compacting soil and ash samples
into 8 inch long (20.3 cm) polyethylene tubes (with dimensions
0.675 in. (16 mm) I.D. by 0.75 in. (19 mm) O.D) and plugged with
two polypropylene end caps. Using groundwater and ash pore
water analytical results from the site, feed solutions amended with
all COIs found above the NCAC 15A 02L .0106(g) standards were
produced and pumped into the columns. Analyses and
equipment used are provided in the table below:
Analyte Method
Trace metals (Sb, As, B, Cd,
Cr, Fe, Mn, Pb, Tl) EPA 200.8
Sulfate EPA 300.0
pH Standard Method 4500 B
Conductivity Standard Method 2510
Oxidation-reduction potential
(ORP) ASTM method G200-19
1.3.1.6.2 Batch Tests
Batch tests were conducted in accordance with U.S.
Environmental Protection Agency Technical Resource Document
EPA/530/SW-87/006-F. COI-amended feed solution (described
above in 1.3.1.6.1) and soil samples were mixed across a range of
soil-to-solution ratios, followed by shaking until chemical
equilibrium was achieved. Once equilibrium was achieved,
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solutions were drawn and analyzed as described in the above
table.
1.3.1.6.3 Hydrous Ferrous Oxides Analysis
The method for HFO determination in soil and ash samples was
adapted from Chao and Zhou (1983). Following this method, soil
samples were extracted using a 0.25M NH2OH·HCl-0.25M HCl
combined solution.
1.3.1.6.4 Ash Leaching Tests
Ash leach tests were performed to provide a basis for estimating
COI source terms to develop the Kd terms. Ash samples were
prepared and analyzed using EPA Method 1313 [2] (Liquid-Solid
Partitioning as a Function of Extract pH Using a Parallel Batch
Extraction Procedure) and EPA Method and EPA Method 1316 [3]
(Liquid-Solid Partitioning as a Function of Liquid-Solid Ratio
using a Parallel Batch Extraction Procedure). Method 1313
provides COI concentration as a function of pH (the test was
conducted only at natural pH). Method 1316 provides COI
concentration as a function of liquid to solid ratio.
1.3.1.7 Index Property Sampling and Analysis
Select soil and ash samples were collected for laboratory analysis of
physical properties to provide data for use in groundwater modeling.
Samples were collected at selected locations for the following analyses
using the described methods:
Natural Moisture Content Determination, in accordance with
ASTM D-2216
Grain size with hydrometer determination, in accordance with
ASTM Standard D-422
In addition, thin-walled undisturbed tubes (“Shelby” tubes) were
advanced in ash and soil at select locations. Undisturbed samples were
tested for the following:
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Natural Moisture Content Determination, in accordance with
ASTM D-2216
Grain size with hydrometer determination, in accordance with
ASTM Standard D-422
Hydraulic Conductivity Determination, in accordance with ASTM
Standard D-5084
Specific Gravity of Soils, in accordance with ASTM Standard D-
854
Sample porosity was calculated from parameters measured during these
tests.
1.3.2 Ash Pore Water and Groundwater Sampling and Analysis
New and existing wells were sampled using low-flow sampling techniques in
accordance with the USEPA Region 1 Purging and Sampling Procedure for the
Collection of Groundwater Samples from Monitoring Wells (revised January 19, 2010),
the Groundwater Monitoring Program Sampling, Analysis and Reporting Plan, L.V.
Sutton Energy Complex (SynTerra, October 2014), updated by the Low Flow
Sampling Plan, Duke Energy Facilities, Ash Basin Groundwater Assessment Program,
North Carolina, June 10, 2015. NCDENR conditionally approved the Low Flow
Sampling Plan in a June 11, 2015 email with an attachment summarizing their
approval conditions.
Equipment blanks for groundwater sampling were collected daily. The sample
was collected from a laboratory-supplied container of deionized water into
laboratory-supplied bottle ware. The equipment consisted of the pump to be
used for sample collection that day and tubing was pulled from the supplies
planned for the day.
Ash pore water and groundwater samples were analyzed in the field and
laboratory. The analytical parameters and associated analytical methods are
summarized on Table 6-3. Only select samples were analyzed for radionuclides
and metals speciation included on Table 6-3. For speciation analysis, select ash
pore water or groundwater samples were collected with a peristaltic pump as
described above but with acid-washed tubing and following a condensed version
of EPA Method 1669.
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2. Hydrogeologic Evaluation Testing
To characterize hydrogeologic conditions, hydrogeologic testing and measurements were
performed. Measurements and testing procedures are discussed below.
2.1 Potentiometric Surface Measurements
During groundwater sampling activities, water level measurements were recorded at
existing site monitoring wells, observation wells, piezometers, and newly installed
wells. The data were used to generate potentiometric maps for each separate
hydrogeologic zone as well as to determine the degree of residual saturation beneath the
ash basin. Water level measurements used for preparation of flow maps were collected
during a single 24-hour period and prior to purging for sampling.
2.2 Slug Tests
After the development and sampling of monitoring wells, hydraulic conductivity tests
(rising head slug tests) were conducted on each of the new wells. Slug tests were
performed in accordance with ASTM D4044-96 Standard Test Method (Field Procedure)
for Instantaneous Change in Head (Slug) Tests for Determining Hydraulic Properties of
Aquifers and NCDENR Performance and Analysis of Aquifer Slug Test and Pumping Test
Policy, dated May 31, 2007.
Prior to the performance of each slug test, static water level was determined and
recorded and a Solinst Model 3001® Edge electronic pressure transducer/data logger, or
equivalent, was placed in a well at a depth of approximately six-inches above the well
bottom. The Levelogger® was connected to a field laptop and programmed with the
well identification, approximate elevation of the well, date, and time.
Slug tests were conducted by lowering a PVC “slug” into a well casing. The water level
within the well was then allowed to equilibrate to a static level. After equilibrium, the
slug was rapidly withdrawn from the well, decreasing the water level in the well
instantaneously. During well recovery, the water level within a well was measured and
recorded electronically using the pressure transducer/data logger. Two separate slug
tests were conducted for each well.
Slug tests were performed for no less than ten minutes, or until such time as the water
level in the well recovered 95 percent of its original pre-test level, whichever occurred
first. Slug tests were terminated after two hours even if the 95 percent pre-test level was
not achieved.
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Data obtained during the slug tests were reduced an analyzed using AQTESOLVTM for
Windows, version 4.5, software to determine the hydraulic conductivity of soils in
vicinity of wells.
3. Screening Level Risk Assessments
To support the groundwater assessment, potential risks to human health and the environment
were assessed in accordance with applicable federal and state guidance. Screening level human
health and ecological risk assessments were conducted that included development of
conceptual exposure models (CEM) to serve as the foundation for evaluating potential risks to
human and ecological receptors. The purpose of the human health and ecological CEMs was to
identify potentially complete exposure pathways to environmental media associated with the
site and to specify the types of exposure scenarios relevant to include in the risk analysis.
Potential exposure pathways were considered complete when all of the following elements
applied: 1) a constituent source; 2) mechanisms of constituent release and transport from the
source area to an environmental medium; and 3) feasible routes of potential exposure at the
point of contact (e.g., ingestion, inhalation, dermal or ambient contact). Maximum constituent
concentrations were compared to appropriate risk-based screening values as a preliminary step
in evaluating potential for risks to human and ecological receptors. Based on results of the
screening level risk assessments, a refinement of COPCs will be conducted and more definitive
risk characterization will be performed as part of the corrective action process if needed.
3.1 Human Health Risk Assessment
The screening level human health risk assessment process involved comparison of
constituent concentrations in various media to the following risk-based screening
criteria:
Soil analytical results collected from the 0 to 2 foot depth interval compared to US
EPA residential and industrial soil Regional Screening Levels (RSLs) (US EPA, June
2015);
Groundwater results compared to NCDENR Title 15A, Subchapter 2L Standards
(NCDENR, 2006);
Surface water analytical results compared to North Carolina surface water standards
(Subchapter 2B) and US EPA national recommended water quality criteria
(NCDENR, 2007; US EPA, 2006).
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The surface water classification as it pertains to drinking water supply, aquatic life,
high/exceptional quality designations and other requirements for other activities
(e.g., landfill permits, NPDES wastewater discharges) were noted;
Sediment results compared to US EPA residential and industrial soil RSLs (US EPA,
October 2014 or latest update); and
Sediment, soil and ground water results compared to available local, regional and
national background sediment, soil and ground water data, as available.
If warranted as part of corrective action decisions, site and media specific risk-based
remediation standards can be calculated in accordance with the Eligibility
Requirements and Procedures for Risk-Based Remediation of Industrial Sites
Pursuant to N.C.G.S. 130A-310.65 to 310.77, North Carolina Department of
Environment and Natural Resources, Division of Waste Management, 29 July 2011.
3.2 Ecological Risk Assessment
The screening level ecological risk assessment (SLERA) for the site included a
description of the ecological setting and development of the ecological CEM specific to
the ecological communities and receptors potentially exposed to site-related COPCs. A
list of potential ecological receptors (e.g., plants, benthic invertebrates, fish, mammals,
birds, etc.) was compiled, as well as identification of sensitive ecological populations and
critical habitat based on information from the North Carolina Natural Heritage Program,
and U.S. Fish and Wildlife Service.
Step 1 of the SLERA consisted of completion of an ecological checklist as required by
Guidelines for Performing Screening Level Ecological Risk Assessment within North
Carolina (NCDENR, 2003).
Step 2 of the SLERA consisted of performing screening level exposure estimates and risk
calculations. This involved comparison of maximum detected concentrations or
maximum detection limits for non-detected constituents to applicable ecological
screening values (ESVs) intended to be protective of ecological receptors. If exposure
concentrations exceeded ESVs, potential ecological impacts could not be ruled out.
The following ESV sources were used in the SLERA:
US EPA Ecological Soil Screening Levels;
US EPA Region 4 Recommended Ecological Screening Values; and
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US EPA National Recommended Water Quality Criteria and North Carolina
Standards.
Constituents were identified as a Step 2 COPCs as follows:
Category 1 – Constituents whose maximum detection exceeded the media-specific
ESV;
Category 2 – Constituents that generated a laboratory sample quantitation limit that
exceeded the US EPA Region IV media-specific ESV;
Category 3 – Constituents with no US EPA Region IV media-specific ESV but were
detected above the laboratory sample quantitation limit;
Category 4 – Constituents that were not detected above the laboratory sample
quantitation limit and had no US EPA Region IV media-specific ESV; and
Category 5 – Constituents with a sample quantitation limit or maximum detection
that exceeded the North Carolina Surface Water Quality Standards.
3.3 Surface Investigation
Samples were collected at the ground or water surface to support the screening level risk
assessment. Samples were collected wearing nitrile gloves.
3.3.1 Surface Water Sampling
Surface water samples were collected to assess groundwater to surface water
pathways and evaluate surface water quality. Sample jars that did not contain a
preservative were used to collect the water directly from the source. The water
was decanted from the sample jars into the jars that required preservative.
Surface water samples were analyzed for parameters listed in Table 6-3, except
for radionuclides and metals speciation parameters. Stream flow measurements
were recorded at the time of sampling with the exception of measurements
within major waterways.
3.3.2 Sediment Sampling
Sediment samples were collected from the bed surface and co-located with
surface and seep samples to evaluate sediment quality and provide data to be
used in the screening level risk assessment. Where possible, samples were
collected directly into sample jars. If surface water was too deep to safely collect
sediment samples directly, sediment was obtained using a sampling dredge.
Sediment samples were analyzed for parameters listed in Table 6-2.
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3.3.3 Seep Sampling
Seep samples were collected wearing nitrile gloves to assess groundwater to
surface water pathways at the site and support the human health and ecological
risk assessment. Seep samples were analyzed for parameters listed in Table 6-3,
except for radionuclides and metals speciation parameters. Seep flow
measurements were recorded at the time of sampling.