HomeMy WebLinkAboutNC0001422_FINAL Sutton CSA Report 08-05-2015_201508056uRE
ENERGY
Auyust 4, 2015
Mr. Donald R. van der vaarff, Secretary
North Carolina Department of Environment and Natural Resuurces
i eui l9lail Service Center
Raleigh, North Carolina 2/ba9-1bul
Subject: uuMPREHENSIVE SITE ASSESSMENT REPORT
Duke Eneryy E.v. Suttun Eneryy Gumplex
Wilmington; New Hanover County, North Carolina
NPDES Permit IQu. NCu001422
Dear Mr. van der Vaart:
Rariy R. saeris
Senior Vice -President
Environmental, I9ealtR & Sarety
526 Suuth Church Street:
Mail Code EC3XP
Charlotte, ivortrl Larolina 25zuz
704-382-4303
In accordance With the %F111 Carolina Department ut Environment and Natural Resources
Division of Water Resources' February 6, 2015 letter (Cnditibnal Approval of 1�rcrvizica
Grou-ndwaafCrASS&Swi i"T WurK Man), DuRe Eneryy hereby submits the Comprehensive Site
Assessment (GSA) Report for the L.V. Sutton E, iv, yy Cumplcx. As inaivatea 6eluw, DuRe
Eneryy is alsu pruvidiny the USA Report to additional NGDENR Central Office personnel, the
NGDENR Wilmington Regional Office, a, id the Cual ASH Manayement Gummissiun.
We consider develupment ana submittal ut tHis GSA Repurt to satisty the directives of your
Gunditional Approval letter as well as the requirements of Suction i 3uA-3u9.2ua(a)(4) ana
Section 13uA-3ua.2u9(d) ut the Cual ASH Manayement Act of 2014.
It yuu Have uumments and/or questions, please direct them to me at 704-382-4303 or Ed
Sullivan, Manager of Waste & Groundwater Pruyrdms, at 98u-3t3-3ily.
Sincerely
Rarry R. Sideris
Senior Vice -President
Environmental, Realth & Safety
Enclosure: Comprehensive Site Assessment Repurt, L.V. Sutton Eneryy Complex
cc. Stanley (Jay) Zimmerman, Director, Division of Water Resources, Central office
Steven Canter; Hydrogeologist, Water Quality Reyiunal upertiuns Section, Central cmice
Turn Reeaer, Assistant Secretary Tor Environment
NGDENR Wilmington Regional Office
Uual Ash Manayement Commission
4cll
synTerra
COMPREHENSIVE
SITE ASSESSMENT REPORT
Site Name and Location:
Groundwater Incident No.:
NPDES Permit No.:
Date of Report:
Permittee and Current
Property Owner:
Consultant Information:
Latitude and Longitude of Facility:
LX Sutton Energy Complex
801 Sutton Steam Plant Road
Wilmington, North Carolina 28401
Not Assigned
NC0001422
August 5, 2015
Duke Energy Progress, Inc.
526 South Church St
Charlotte, NC 28202
(980) 373-3719
SynTerra
148 River Street
Greenville, South Carolina
(864) 421-9999
N 34.283296 / W-77.985860
/ Perry Wrep
a
for Project eager
Webb, NC PG 1328
Project Director
INNOVATE 148 River Street, Suite 220 Greenville, SC 29601 (864)421-9999 Fax (864)421-9909 www.synterracorp.com
DIVISION OF WATER RESOURCES
Certification for the Submittal of a Comprehensive Site Assessment
Responsible Party and/or Permittee: Duke Energy Progress, Inc.
Contact Person: Harry Sideris
Address: 526 South Church Street
City: Charlotte State: NC Zip Code: 28202
Site Name: L.V. Sutton Energy Complex
Address: 801 Sutton Steam Plant Road
City: Wilmington State: NC Zip Code: 28401
Groundwater Incident Number (applicable): NA/ Coal Ash Management Act CSA
I, Kathy Webb, a Professional Engineer/Professional Geologist (circle one) for
SynTerra Corporation (firm or company of employment) do hereby certify that the
information indicated below is enclosed as part of the required Comprehensive Site
Assessment (CSA) and that to the best of my knowledge the data, assessments,
conclusions, recommendations and other associated materials are correct, complete
and accurate.
(Each i m must be initialed by the certifying licensed professional)
1. The source of the coal combustion residuals (contamination) has been identified. A list
of all potential sources of the coal combustion residuals (contamination) is attached.
2. Imminent hazards to public health and safety have been evaluated.
3. Potential receptors and significant exposure pathways have been identified
4. Geological and hydrogeological features influencing the movement of groundwater have
been identified. The chemical and physical character of the contaminants have been
identified.
5. The CSA sufficiently characterizes the cause, significance and extent of groundwater and
soil contamination associated with the regulated coal ash management areas such
that a groundwater Corrective Action Plan can be developed.
If any of the above statements have been altered or items not initialed,
provide a detailed explanation. Failure to initial any item or to provide
written justification for the lack thereof will result in immediate return of the
CSA to the responsible party.
(Please Alix Seal and Signature)
SIA w
OGI
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Item 1. The CSA was specifically designed to assess the coal ash management
areas of the facility. Sufficient information is available to prepare the
groundwater corrective action plan for the ash management areas of the
facility. Data limitations are discussed in Section 14 of the CSA report.
Continued groundwater monitoring at the site is planned.
Item 2. Imminent hazards to human health and the environment have been
evaluated. The NCDENR data associated with nearby water supply wells
is provided herein and is being evaluated. In the meantime, plans are
underway to replace the nearby public water supply system and to install
an interim groundwater corrective action plan.
Item 5. The groundwater assessment plan for the CSA as approved by NCDENR
was specifically developed to assess the coal ash management areas of
the facility for the purposes of developing a corrective action plan for
groundwater. Other areas of possible contamination on the property were
not evaluated.
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Comprehensive Site Assessment Report August 2015
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L.V. SUTTON ENERGY COMPLEX
EXECUTIVE SUMMARY
The North Carolina Coal Ash Management Act (CAMA) requires the preparation of a
Comprehensive Site Assessment (CSA) Report for each regulated facility within 180
days of approval of the Work Plan. This report addresses Duke Energy’s L.V. Sutton
Energy Complex (Site). The Work Plan for the Site was approved on February 6, 2015.
The purpose of this assessment is to identify the source and cause of exceedances of
regulatory standards, potential hazards to public health and safety, receptors and
exposure pathways.
NC Department of Environment and Natural Resources (NCDENR) prescribed the list
of monitoring parameters to be measured at the Site. Once the sampling portion of the
CSA was complete, data were examined to pick those parameters that were most
relevant to the Site. These parameters were determined by examining data from
monitoring wells installed in ash, and then by comparing these results to 2L or the
former Interim Maximum Allowable Concentrations (IMACs). Appendix #1 of 15A
NCAC Subchapter 02L Classifications and Water Quality Standards Applicable to The
Groundwaters of North Carolina, lists 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.
Parameters detected in ash pore water samples at values greater than 2L or IMAC, were
designated as a ‘Constituent of Interest’ (COI). Some COIs (e.g., iron and manganese)
are also present in background monitoring wells and thus require careful examination
to determine whether their presence on the downgradient side of a basin is from natural
sources (e.g., rock and soil) or the ash basin.
This assessment addresses the horizontal and vertical extent of COIs in soil and
groundwater, significant factors affecting groundwater flow conditions, and the
geological and hydrogeological features influencing the movement, chemical, and
physical character of COIs.
Data presented in this assessment report is the basis for the Corrective Action Plan
(CAP) required within 270 days of the approved Work Plan to identify alternative
strategies to address groundwater impacts at the site.
The Corrective Action Plan, as required by CAMA, will include groundwater model
results of the anticipated ash removal to assess the effects on groundwater. A
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groundwater monitoring plan will be provided to assess changes in groundwater
conditions over time.
In accordance with CAMA Section 3(b), Duke Energy will fully excavate the ash basins
at the Site, with the material to be safely recycled or reused in a lined structural fill or
disposed in a lined landfill. Additionally, a Groundwater Mitigation and Monitoring
Plan was submitted to NCDENR in July 2015 which proposed a groundwater extraction
system as an interim corrective action to address the migration of COIs.
Based on the evaluation of both historical and recently obtained CSA data, the
following conclusions are provided:
Recent groundwater assessment results are consistent with previous results from
historical and routine compliance boundary monitoring well data.
Background monitoring wells contain naturally occurring COIs at concentrations
greater than 2L or former IMAC. This information is used to evaluate whether
concentrations in groundwater downgradient of the basins are naturally
occurring, from another source or influenced by migration of constituents from
an ash basin. As examples, iron, manganese, cobalt and vanadium are present in
the background monitor well samples at concentrations at or above their
applicable 2L or IMAC.
Regional groundwater flow is to the west toward the Cape Fear River, to the east
toward the Northeast Cape Fear River or to the south toward the convergence of
the two rivers. In the vicinity of the 1971 and 1984 ash basins, groundwater
flows radially. A groundwater divide is located northeast of the ash basins and
groundwater north of the basins flow west toward the cooling pond.
Groundwater east and south of the basins flows east, southeast and south. In the
Former Ash Disposal Area (FADA), groundwater flows to the southwest.
Data indicate the water quality of the Cape Fear River has not been impacted by
the ash basins.
Migration of COIs, primarily boron, above the 2L, has occurred in the lower
surficial aquifer at a depth of approximately 25 to 50 feet below ground surface.
Concentrations of boron in the ash pore water and groundwater adjacent to the
1971 ash basin are higher than elsewhere on the Site. Also, boron concentrations
are not observed in surficial aquifer background wells and concentrations
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decrease downgradient of the basins; thus, boron serves as a good indicator of
the maximum extent of ash constituent migration. However, boron has also been
detected in deeper Pee Dee formation wells at the site. This is likely a result of
saltwater intrusion (boron is the 10th most prevalent constituent in sea water).
Regional groundwater data supports this.
Boron is detectable above the 2L in offsite monitoring wells downgradient and
east of the basins. The horizontal extent of the boron concentrations above the 2L
has been defined. Boron concentrations greater than 2L do not extend southeast
to the public water supply wells located beyond the property boundary
southeast of the basins. The approximate extent of horizontal migration of boron
is shown on Figure ES-1.
The flow paths for COIs indicate a preference for lateral migration, rather than
vertical migration, as a result of contrasting hydraulic conductivities between the
surficial and Pee Dee formations. A clay confining unit was not observed in the
monitoring wells or soil borings within the study area. While no confining unit
is present above the Pee Dee Formation, the lower permeability of the Pee Dee
Formation reduces vertical migration of COIs.
The CSA characterizes the horizontal and vertical extent of COIs and
groundwater gradients which now facilitate development of the Site Conceptual
Model (SCM) (i.e., the groundwater flow and constituent migration model). This
then facilitates development of a CAP due within 90 days of submittal of this
CSA report.
The horizontal extent of boron in the lower surficial aquifer at levels exceeding
the 2L has extended beyond the site boundary to the east. Mitigating actions to
address this horizontal extent are already initiated.
o An interim corrective action plan has been prepared and submitted to
NCDENR. The interim plan proposes 12 groundwater extraction wells
along the downgradient property line to intercept the groundwater in the
area of boron migration.
o Data indicate boron concentrations in nearby water supply wells are less
than the 2L.
o The approximate extent of horizontal migration of boron in the surficial
aquifer is shown on Figure ES-1.
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Brief summaries of portions of the Comprehensive Site Assessment report are presented
in the following sections.
ES.1 Source Information
Mineralogical, physical, and chemical properties of the Site ash basins have been
characterized for use in the hydrogeological SCM. The ash management area consists
of three locations; the FADA, the 1971 ash basin and the 1984 ash basin. The FADA,
which contains a depth of ash less than 15 feet, is located in a low-lying area and was
developed near original ground surface. The 1971 ash basin was excavated to a depth
of approximately 40 feet below ground surface (bgs) and contains approximately 80
vertical feet of ash at its deepest point. The 1984 ash basin was constructed near
original ground surface and contains a clay liner. Groundwater within the 1971 and
1984 basins is mounded and hydraulically upgradient of the surrounding land surface
to the northeast, east and southeast and the normal pool elevation of the cooling pond
located to the west. Seepage of water from within the 1971 and 1984 ash basins to
groundwater under the basins migrates in a radial pattern.
ES.2 Initial Abatement and Emergency Response
Duke Energy is currently planning to fully excavate the ash basins in accordance with
CAMA requirements; with the material safely recycled or reused in a lined structural
fill or disposed in a lined landfill. A Groundwater Mitigation and Monitoring Plan was
submitted to NCDENR in July 2015 to address offsite migration of constituents of
concern, primarily boron. Twelve extraction wells are proposed along the eastern site
boundary to intercept groundwater in the surficial aquifer. Plans to discontinue the use
of the nearby municipal water supply wells are underway and Duke has taken
proactive steps to replace these water supply wells with a new water line extension.
Completion of the replacement well field water system is anticipated by December
2015.
ES.3 Receptor Information
Land use surrounding the Site includes commercial, industrial, mining (sand quarry),
residential, and forest land. The Site is located on a small peninsula formed by the Cape
Fear River bordering the Site to the west and the Northeast Cape Fear River located
approximately one mile to the east. The two rivers converge in the City of Wilmington
south of the Site.
Well inventories of public and private wells have been compiled. Nearby property
owners have been contacted regarding private wells and a number of water supply
wells have been sampled at the direction of NCDENR. Inventories of public and
private water supply wells have been updated as part of this assessment. The
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groundwater model being developed for the Site will provide additional information on
the likelihood of private and public wells being impacted by the Site.
ES.3-1 Public Water Supply Wells
Four Cape Fear Public Utility Authority (CFPUA) municipal water supply wells
are located near the southeastern property boundary of the site. Two of these
wells are not in use. Analyses on samples collected routinely from the wells
indicate concentrations of manganese slightly above the 2L. Data indicate these
exceedances are not related to the ash basins. The CFPUA wells are
approximately 50 feet deep within the surficial sand aquifer. These two wells
will be eliminated once the new water line is completed in December 2015. After
which, all four wells will be properly abandoned.
ES.3-2 Private Water Supply Wells
Inventories of other smaller public and private water supply wells have been
compiled. NCDENR contacted nearby property owners regarding water supply
wells and managed the sampling of the wells in accordance with CAMA. Water
supply wells are located within 0.5 mile of the site, including on-site wells used
for plant operations and wells for commercial and industrial developments.
Some of the wells are production wells that might also be used as a source of
drinking water as there are no public water lines to these facilities.
While some of these wells are potentially located downgradient to the site, and
2L or IMAC were exceeded in some samples for iron, manganese, cobalt and
vanadium, these constituents are common to groundwater in the region and
their occurrence cannot be conclusively attributed to the ash basins. Where
industrial water supply wells are located in the area mapped with boron 2L
exceedances based upon monitoring well data, the water supply well sample
data provided by NCDENR indicate the boron concentrations are not greater
than the 2L for the production well samples.
ES.3-3 Human and Ecological Receptors
Consumption of groundwater, recreational use of affected surface water
(particularly ‘Lake Sutton’ located west of the ash basins, built as the plant
cooling pond but open to the public for fishing) and consumption of fish and
game potentially affected by these waters are the primary potential exposure
pathways for humans in the vicinity of the ash basins.
The ecological exposure medium includes potentially impacted soil, surface
water and sediments at the site. Groundwater does not present a complete
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exposure pathway to ecological receptors. Potentially complete pathways
evaluated for the Site include incidental ingestion of soil or sediment, and
ingestion of prey or plants.
The Cape Fear River Basin supports over 95 species of commercial and
recreational fish, including 42 rare aquatic species. The Cape Fear shiner
(Notropis mekistocholas), a federally endangered fish species, is known only to
inhabit this river basin. The shortnose sturgeon (Acipenser brevirostrum), red-
cockaded woodpecker (Leuconotopicus borealis), Saint Francis’ satyr (Neonympha
mitchellii francisci), and the West Indian manatee (Trichechus manatus) (in
estuarine areas) are also known species in the Cape Fear River and are federally
listed as endangered. The American alligator (Alligator mississippiensis) and the
loggerhead turtle (Caretta caretta) are federally listed as threatened.
ES.4 Sampling / Investigation Results
ES.4-1 Nature and Extent of Contamination
Arsenic, barium, boron, cobalt, iron, manganese, selenium, thallium, vanadium
and total dissolved solids (TDS) have been identified as site specific COIs based
on concentrations in excess of the 2L or IMAC in the saturated ash (pore) water
or groundwater. Iron, manganese and vanadium were detected in the ash pore
water, however these are naturally-occurring metals common to regional
groundwater and their occurrence at the Site cannot be wholly attributed to the
ash basins. Cobalt and thallium were not detected in ash pore water samples,
therefore the concentrations in groundwater appear to be naturally occurring.
Selenium occurs in groundwater in an isolated area north of the ash basins;
however it was not detected in the 1971 ash basin pore water. Groundwater data
immediately north of the 1984 ash basin can be collected to determine if it is the
source of the selenium in this area of the Site.
Historical groundwater monitoring has shown that values for iron and
occasionally manganese can be greater than the 2L in background wells. Site
specific historical data are not available for vanadium. However, iron,
manganese and vanadium are known to be commonly occurring in background
shallow groundwater in the coastal plain region of North Carolina. Manganese
and cobalt were detected in background wells MW-37B/C and MW-5C and iron
and vanadium were detected in MW-37B/C at concentrations greater than 2L or
IMAC. Arsenic in groundwater at concentrations greater than the 2L is limited
to an area southeast of the 1971 ash basin and below the FADA.
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Boron is detectable above the 2L in offsite monitor wells directly east and
downgradient of the basins. The horizontal extent of the boron concentrations
above the 2L has been defined. Boron concentrations greater than the 2L do not
extend southeast to the public water supply wells located beyond the property
boundary. The horizontal extent of boron in groundwater greater than the 2L is
shown on Figure ES-1. Field observations indicate that the Pee Dee formation is
not associated with a clay-confining layer at the site; however the low
permeability of the Pee Dee formation, based on hydraulic conductivity values,
contrasts with that of the overlying surficial sands and acts as an aquitard to
downward vertical flow.
ES.4-2 Maximum Contaminant Concentrations
For the COIs identified on the basis of basin ash pore water concentrations,
boron, iron, manganese and vanadium are the most prevalent in groundwater.
Iron, manganese and vanadium were also detected in background wells and the
occurrence of these metals can also be attributed to regional groundwater
quality. Of these, boron is the only COI that is not typical of surficial aquifer
background conditions and attributed to the ash basins in the surficial aquifer
wells.
The highest concentration of boron in groundwater was detected in MW-23C, a
compliance boundary well screened in the lower surficial aquifer and located 500
feet east of the 1971 ash basin. The boron concentration in MW-23C was 3,060µg/l
in March 2015 and 2,050µg/l in June 2015.
The highest concentration of arsenic in groundwater occurs beneath the FADA.
Higher concentrations were detected in the 1971 ash basin pore water well,
which is screened below the water table but is not considered groundwater. The
CSA data indicate that arsenic migration in groundwater is limited to the FADA
waste boundary and an area just southeast of the 1971 ash basin (MW-21C).
The highest concentration of iron in groundwater was detected in a sample from
SMW-2B, an offsite monitoring well screened in the upper surficial aquifer and
located approximately 800 feet east of the site property boundary. The iron
concentration at this location is interpreted to be unrelated to the ash basins
based on the distribution of iron concentrations across the site. Similar high iron
concentrations were also detected in other offsite monitor wells and wells located
along the eastern site boundary or upgradient to the ash basins; suggesting the
iron is naturally-occurring or related to an offsite source.
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The highest concentration of manganese in groundwater was also detected in a
sample from an offsite well, SMW-3C, screened in the lower surficial aquifer and
located approximately 900 feet east of the site property boundary. The
distribution of manganese is similar to that of iron and is also considered to be
unrelated to the ash basins.
The highest concentrations of TDS in groundwater were detected in the Pee Dee
Formation wells and in surficial wells located along the eastern property
boundary. The highest concentration of vanadium in groundwater was 39.6 µg/l
detected in a sample collected from MW-20, a well screened in the upper surficial
aquifer located southwest and downgradient of the FADA.
Cobalt was not detected in the ash pore water and as such its occurrence in
several wells at the site is not considered related to the ash basins. The highest
concentration of cobalt in groundwater, 93.1µg/l, was detected in SMW-2C; an
offsite well which is screened in the lower surficial aquifer and located east of the
site property boundary.
Selenium was not detected in the ash pore water and is only detected in two
wells. Additional data associated with the 1984 basin is needed to rule it out as a
possible source of the selenium.
Exceedances of 2B concentrations were detected in the surface water samples for
aluminum, copper, iron and zinc. Aluminum and copper exceedances were
detected in samples collected from the cooling pond. Aluminum was detected
above the 2B concentration in samples collected from the Cape Fear River at
locations upgradient, adjacent and downgradient to the ash basins, while zinc
was detected above the 2B concentration in upgradient samples.
ES.4-3 Source Characterization
Ash within the basins and the FADA are the source of COIs in groundwater,
primarily boron. Ash disposal in the FADA ended in 1971 and sluicing of ash to
the 1971 and 1984 basins was discontinued in 2013. The ash within the FADA is
less than 15 feet thick and groundwater in the FADA is approximately three feet
bgs. The underlying soils in the FADA consist of the medium-fine grained sands
of the surficial aquifer.
The ash in the 1971 basin is approximately 80 feet thick. The 1971 ash basin area
appears to have been excavated below grade to a depth of approximately 40 feet
and all but the lower couple of feet of the surficial sands were removed prior to
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placement of the ash. The Pee Dee Formation underlies the remnant surficial
aquifer sands below the ash basin. The water level recorded in the 1971 basin
was approximately 34 feet bgs and therefore ash below this depth is saturated.
When the 1971 ash basin was operational, the discharge was routed to the
cooling pond. The cooling pond outfall to the Cape Fear River is regulated
under a NPDES permit. The 1971 ash basin continues to receive rainwater and
storm water runoff from the plant, which infiltrates into the subsurface of the ash
basin. No runoff or discharge occurs from the ash basin.
The 1984 ash basin was constructed with a 12-inch thick clay liner. Therefore,
drilling into or through the clay liner to collect similar data for the 1984 basin
was not conducted.
ES.4-4 Receptor Survey
A receptor survey was conducted in accordance with CAMA during 2014 and
has been updated herein with additional available information.
Public water supply wells in New Hanover County draw water from the surficial
aquifer. The closest public water supply wells are two active wells located to the
southeast of the ash basins and the property line. These wells are routinely
sampled. No COIs are detected above the 2L in the public supply wells with the
exception of manganese. Based on data obtained during the assessment, the
occurrence of manganese in the area of the public supply wells cannot be
conclusively attributable to the ash basins.
Other water supply wells identified within ½ mile of the compliance boundary
are located east and southeast of the site. During 2015, NCDENR managed the
sampling of water supply wells in the area. Only iron, manganese, cobalt, and
vanadium were reported at concentrations greater than 2L or IMAC. Based on
data obtained during the assessment, the occurrence of iron, manganese and
cobalt in the wells cannot be directly attributed to the ash basins. Vanadium is
also a naturally-occurring element in groundwater and assessment data does not
definitively indicate a connection between the detection of vanadium in the
supply wells and the ash basins. Boron results for the water supply wells
sampled at the direction of NCDENR were reported to be less than the 2L.
Constituents of potential concern (COPCs) for human and ecological receptors
identified using screening level risk assessment methodology include aluminum,
antimony, arsenic, barium, beryllium, boron, cadmium, sulfide, TDS, chromium,
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copper, iron, lead, manganese, molybdenum, selenium, thallium, vanadium, and
zinc. This list is longer than the list of site COIs due to the conservative approach
of comparing analytical results to published reference values in the risk
assessment screening process. Additional risk evaluation will be provided as
part of the CAP.
ES.4-5 Regional Geology and Hydrogeology
The Site lies within the Coastal Plain Physiographic Province. The Coastal Plain
comprises a wedge shaped sequence of stratified marine and non-marine
sedimentary material deposited on crystalline basement. In the eastern part of
the North Carolina Coastal Plain, groundwater is obtained from the surficial,
Castle Hayne, and Pee Dee aquifers, although the Castle Hayne is not present in
the area of the Site. The Coastal Plain groundwater system consists of aquifers
comprised of permeable sands, gravels, and limestone separated by confining
units of less permeable material.
ES.4-6 Site Geology and Hydrogeology
Soils exposed at the surface in the Site area are relatively recent Coastal Plain
sediments. Sediments of the surficial aquifer are underlain unconformably by
the unconfined Pee Dee Formation at approximately 50 feet below land surface.
No confining unit was found between the surficial aquifer and the Pee Dee
Formation at the site. However, data indicate lower hydraulic conductivities in
the Pee Dee formation than in the overlying surficial aquifer, indicating the Pee
Dee acts as an aquitard to vertical migration.
The site is located on a peninsula of land defined by the Cape Fear River,
adjacent to the west and the Northeast Cape Fear River, located approximately
one mile to the east. Based on regional topography and drainage features,
groundwater flow within this peninsula would be either west or east to one of
the two rivers or to the south where the rivers converge. At the site, the current
interpretation of groundwater flow indicates that in close proximity to the 1971
and 1984 ash basins, groundwater flows radially; toward the west along the edge
of the cooling pond and to the east, southeast and south on the east side of the
1971 ash basin. In the FADA, groundwater flow is to the southwest. A
groundwater divide or ridge is located northeast of the ash basins. Areas where
shallow water levels appear to be influenced by operating water wells occur near
the plant production wells, which are used for industrial purposes, the CFPUA
(public water supply) wells, located southeast of the site, and the Wooten plant
production wells, located directly to the east of the ash basins.
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Depth to the water table is approximately 7 to 18 feet below land surface. The
potential influence of on-site production wells, off-site municipal and industrial
production wells is being evaluated with the groundwater flow model to be
presented with the CAP. The model results will be used to further assess the
groundwater flow directions at the site. As the model is being prepared,
additional groundwater and surface water elevation data may be collected.
ES.4-7 Existing Groundwater Monitoring Data
The compliance monitoring data indicate that iron has been consistently detected
at concentrations greater than the 2L for background well MW-4B, while
manganese has been detected at a concentration greater than 2L intermittently.
Manganese is consistently detected at a concentration greater than the 2L at the
southern compliance well MW-7C.
Manganese is typically the only constituent detected at a concentration greater
than the 2L at background well MW-5C, to the north of the basins. Manganese
and selenium are consistently detected at concentrations greater than the 2L at
the northern compliance boundary well MW-27B.
Boron, iron, and manganese have been detected at concentrations greater than
the 2L in eastern compliance wells MW-19, MW-21C, MW-22B, MW-23C and
MW-24C.
ES.4-8 Development of Site Conceptual Model
A hydrogeological site conceptual model was developed from data generated
during previous assessments, existing groundwater monitoring data, and 2015
groundwater assessment activities. In general, the ash basin pore water seeps
directly into the porous sands of the surficial aquifer underneath the unlined
1971 ash basin and the FADA. It is anticipated that some migration may occur
from the lined basin, however to a lesser extent. The contrast of permeabilities
across the surficial/Pee Dee contact reduces downward vertical groundwater
flow. The highest concentrations of COIs are detected in the lower surficial
aquifer at a depth of approximately 45 feet, above the surficial/Pee Dee contact.
The horizontal extent of boron in the surficial groundwater flow zone greater
than 2L is shown on ES-1.
ES.5 Identification of Data Gaps
The horizontal and vertical extent of COIs have been sufficiently determined for soil
and groundwater. Source area and groundwater characterization data will be used to
support preparation of flow and transport groundwater modeling for the site. The site
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conceptual model provided herein will also support the modeling and the preparation
of the CAP. There are no data gaps that will be limiting factors in the execution of the
groundwater model or development of the CAP.
However, the following additional information would be useful:
1. Determination of background COI concentrations for deep (Pee Dee formation)
groundwater.
2. Evaluation of potential offsite sources or natural conditions related to the
concentrations of iron and manganese.
3. Further evaluation of the 1984 basin as a potential source of the selenium in the
groundwater north of the ash basin.
ES.6 Conclusions
Duke Energy plans to excavate the ash basins at the Site in accordance with CAMA
requirements. The impact of the ash excavation on long term groundwater quality will
be evaluated as part of the groundwater flow and transport modeling to be provided in
the Corrective Action Plan.
Data indicate groundwater has been impacted by the seepage of ash pore water from
the unlined 1971 ash basin and FADA. The lined ash basin may also contribute to this
impact, but to a lesser extent. Detectable boron concentrations have migrated offsite to
the east. However, the 2015 data collected by NCDENR indicate the boron
concentrations in the public and private water supply wells sampled are less than 2L.
The extent of the boron concentrations greater than 2L in the surficial aquifer has been
defined. The anticipated horizontal and vertical extent of potential migration will be
further evaluated by the groundwater modeling to be provided in the CAP.
A Groundwater Mitigation and Monitoring Plan has been submitted to protect water
supply wells located east of the site. The plan includes the installation of 12
groundwater extraction wells along the eastern property boundary. Groundwater
modeling to be provided in the CAP will also evaluate this action combined with
removal of the ash from the basins.
A plan for future groundwater monitoring is presented in Section 16 of this report. The
Corrective Action Plan, based on the data presented in this report and subsequent
groundwater modeling, will be submitted within 90 days of this report.
#
#
#
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")")
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U
S-421
S
R-2
1
6
9
P R J -I -1 4 0
SR-1394
S R -2 7 7 9
S R -2 1 4 5
P R J -I -1 4 0
FORMER ASHDISPOSAL AREA
1984 ASHBASIN(LINED)
NEW ASHBASIN AREA(LINED)
1971 ASHBASIN
COOLINGPOND
COOLINGPOND
COOLINGPOND
COOLINGPOND
CAPE FEARRIVER
DRAINAGECHANNEL
COOLINGPOND
COOLING PONDCOOLING POND
FIGURE ES-1SITE CONCEPTUAL MODEL - PLAN VIEWL.V. SUTTON ENERGY COMPLEX
±
WATER SUPPLY WELLS1
WATER SUPPLY WELL IN INVENTORY (APPROXIMATE)
WOOTEN PRODUCTION WELL (APPROXIMATE)
#CFPUA PRODUCTION WELL LOCATION (APPROXIMATE)
EDR REPORTED WELL LOCATION (APPROXIMATE)
INVISTA PRODUCTION WELL (APPROXIMATE)
")DUKE ENERGY PROGRESSS PRODUCTION WELL (APPROXIMATE)
P:\D uke Energy Progress.1026\00 GIS BASE DATA\Sutton\Map_Docs\Draft_CSA_v07152015\Sutton - Figure ES-1 - Executive Summary Figure.mxd
L. V. SUTTON ENERGY COMPLEX801 SUTTON STEAM PLANT RDWILMINGTON, NORTH CAROLINA
148 RIVER STREET, SUITE 220GREENVILLE, SC 29601864-421-9999www.synterracorp.com
GRAPHIC SCALE
500 0 500 1,000 1,500 2,000
(IN FEET)
PROJECT MANAGER: J. MAHAN
DRAWN BY: J. MEADOWS
DATE: 07/31/2015
DATE: 07/31/2015
CHECKED BY: K. WEBB
NOTES:1 FROM DRINKING WATER WELL AND RECEPTOR STUDY (NOVEMBER 2014).
2 BORON EXHIBITS THE GREATEST THREE-DIMENSIONAL EXTENT OFMIGRATION FROM THE L.V. SUTTON ENERGY COMPLEX ASH BASIN. THE NORTHCAROLINA 2L (NC2L) FOR BORON IS 700 μg/L.
3 APRIL 17, 2014 AERIAL ORTHOPHOTOGRAPHY OBTAINED FROM WSP.
4 2012 AERIAL ORTHOPHOTOGRAPHY OBTAINED FROM THE NC CENTER FORGEOGRAPHIC INFORMATION AND ANALYSIS. (http://services.nconemap.gov/)
5 PARCEL BOUNDARY WAS OBTAINED FROM THE NC CENTER FORGEOGRAPHIC INFORMATION AND ANALYSIS. (http://services.nconemap.gov/)
6 DRAWING HAS BEEN SET WITH A PROJECTION OF NORTH CAROLINA STATEPLANE COORDINATE SYSTEM FIPS 3200 (NAD83/2011).
AREA OF CONCENTRATIONS IN GROUNDWATER ABOVE NC2L 2
GROUNDWATER FLOW DIRECTION (SHALLOW AQUIFER)
ASH BASIN BOUNDARY
ASH BASIN COMPLIANCE BOUNDARY
HAL F-MILE OFFSET FROM COMPLIANCE BOUNDARY
DUKE ENERGY PROGRESS SUTTON PLANT SITE BOUNDARY
LEGEND
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TABLE OF CONTENTS
SECTION PAGE
L.V. Sutton Energy Complex Executive Summary ................................................................ i
ES.1 Source Information ........................................................................................................ iv
ES.2 Initial Abatement and Emergency Response ........................................................... iv
ES.3 Receptor Information .................................................................................................... iv
ES.3-1 Public Water Supply Wells ................................................................................. v
ES.3-2 Private Water Supply Wells ............................................................................... v
ES.3-3 Human and Ecological Receptors ...................................................................... v
ES.4 Sampling / Investigation Results ................................................................................ vi
ES.4-1 Nature and Extent of Contamination ............................................................... vi
ES.4-2 Maximum Contaminant Concentrations ........................................................ vii
ES.4-3 Source Characterization ................................................................................... viii
ES.4-4 Receptor Survey .................................................................................................. ix
ES.4-5 Regional Geology and Hydrogeology .............................................................. x
ES.4-6 Site Geology and Hydrogeology ....................................................................... x
ES.4-7 Existing Groundwater Monitoring Data ......................................................... xi
ES.4-8 Development of Site Conceptual Model .......................................................... xi
ES.5 Identification of Data Gaps ......................................................................................... xi
ES.6 Conclusions .................................................................................................................... xii
1.0 Introduction ..................................................................................................................... 1
1.1 Purpose of Comprehensive Site Assessment ......................................................... 2
1.2 Regulatory Background ............................................................................................ 2
NCDENR Requirements ..................................................................................... 2 1.2.1
NORR Requirements ........................................................................................... 2 1.2.2
Coal Ash Management Act Requirements ....................................................... 2 1.2.3
1.3 NCDENR-Duke Energy Correspondence .............................................................. 3
1.4 Approach to Comprehensive Site Assessment ...................................................... 4
NORR Guidance ................................................................................................... 4 1.4.1
USEPA Monitored Natural Attenuation Tiered Approach ........................... 4 1.4.2
ASTM Conceptual Site Model ............................................................................ 5 1.4.3
1.5 Technical Objectives .................................................................................................. 5
2.0 Site History and Description ........................................................................................ 6
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2.1 Site Location, Acreage, and Ownership ................................................................. 6
2.2 Plant Description ........................................................................................................ 6
2.3 General Site Description ........................................................................................... 7
2.4 Adjacent Property, Zoning, and Surrounding Land Uses ................................... 7
2.5 Adjacent Surface Water Bodies and Classifications .............................................. 7
2.6 Meteorological Setting ............................................................................................... 7
2.7 Hydrologic Setting ..................................................................................................... 8
2.8 Permitted Activities and Permitted Waste ............................................................. 8
2.9 History of NPDES and Surface Water Monitoring ............................................... 8
2.10 Assessment Activities or Previous Site Investigations ......................................... 9
2.11 Corrective Actions ................................................................................................... 12
3.0 Source Characteristics .................................................................................................. 13
3.1 Coal Combustion and Ash Handling System ...................................................... 13
3.2 Physical Properties of Ash ...................................................................................... 13
3.3 Chemical Properties of Ash .................................................................................... 13
3.4 Description of Ash Basins and Other Ash Storage Areas .................................. 15
4.0 Receptor Information ................................................................................................... 17
4.1 Summary of Receptor Survey Activities............................................................... 17
4.2 Summary of Receptor Survey Findings ................................................................ 18
Public Water Supply Wells ............................................................................... 18 4.2.1
Private Water Supply Wells ............................................................................. 19 4.2.2
5.0 Regional Geology and Hydrogeology ...................................................................... 20
5.1 Regional Geology ..................................................................................................... 20
5.2 Regional Hydrogeology .......................................................................................... 20
6.0 Site Geology and Hydrogeology ................................................................................ 22
6.1 Site Geology .............................................................................................................. 25
Soil Classification ............................................................................................... 25 6.1.1
Rock Lithology ................................................................................................... 26 6.1.2
Structural Geology ............................................................................................. 26 6.1.3
Soil and Rock Mineralogy and Chemistry ..................................................... 26 6.1.4
6.2 Site Hydrogeology ................................................................................................... 26
Groundwater Flow Direction ........................................................................... 27 6.2.1
Hydraulic Gradients .......................................................................................... 28 6.2.2
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Hydraulic Conductivity .................................................................................... 28 6.2.3
Groundwater Velocity ....................................................................................... 28 6.2.4
Effects of Geologic/Hydrogeologic Characteristics on Contaminants ....... 29 6.2.5
6.3 Hydrogeologic Site Conceptual Model ...................................................................... 29
6.4 Geochemical Site Conceptual Model .................................................................... 30
Iron ....................................................................................................................... 30 6.4.1
Vanadium ............................................................................................................ 30 6.4.2
Manganese .......................................................................................................... 31 6.4.3
Boron .................................................................................................................... 31 6.4.4
Arsenic ................................................................................................................. 33 6.4.5
Cobalt ................................................................................................................... 33 6.4.6
6.5 Electrochemical Charge Balance ............................................................................ 33
6.6 Equilibrium ............................................................................................................... 34
7.0 Source Characterization ............................................................................................... 36
7.1 Identification and Description of Sources ............................................................ 36
Coal Combustion and Ash Handling System ................................................ 36 7.1.1
Description of Ash Basins ................................................................................. 36 7.1.2
7.2 Characterization of Sources .................................................................................... 37
Physical Properties of Ash ................................................................................ 37 7.2.1
Chemical Properties of Ash .............................................................................. 38 7.2.2
Chemistry of Ash Pore Water .......................................................................... 39 7.2.3
Hydrology of the Ash Basins ........................................................................... 39 7.2.4
7.3 Piezometers and Seeps ............................................................................................ 40
7.4 Constituents of Interest ........................................................................................... 41
8.0 Soil and Rock Characterization .................................................................................. 42
8.1 Background Soil ....................................................................................................... 43
Soils beneath the Ash Basin .............................................................................. 43 8.1.1
Site Soils ............................................................................................................... 44 8.1.2
Surficial Soils....................................................................................................... 44 8.1.3
8.2 Comparison of Results to Applicable Levels ....................................................... 45
9.0 Sediment and Surface Water Characterization ....................................................... 46
9.1 Comparison of Exceedances to 2B Standards ...................................................... 46
9.2 Discussion of Results for Constituents Without Established 2B ....................... 47
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10.0 Groundwater Characterization ................................................................................... 48
10.1 Background Groundwater Conditions ................................................................. 48
10.2 Discussion of Redox Conditions ............................................................................ 48
10.3 Regional Groundwater Data for Constituents of Potential Concern................ 49
10.4 Groundwater Analytical Results ........................................................................... 49
10.5 Comparison of Results to 2L Standards ............................................................... 53
11.0 Hydrogeological Investigation ................................................................................... 55
11.1 Hydrostratigraphic Layer Development .............................................................. 55
11.2 Hydrostratigraphic Layer Properties .................................................................... 55
Confining Unit .............................................................................................. 55 11.2.1
In-Situ Tests ................................................................................................... 56 11.2.2
Slug Tests ....................................................................................................... 56 11.2.3
Porosity .......................................................................................................... 56 11.2.4
11.3 Groundwater Flow Direction ................................................................................. 56
11.4 Hydraulic Gradient .................................................................................................. 57
11.5 Groundwater Velocity ............................................................................................. 57
11.6 Contaminant Velocity .............................................................................................. 57
11.7 Characterization of COI Distribution .................................................................... 57
11.8 Groundwater / Surface Water Interaction ............................................................ 57
12.0 Screening-Level Risk Assessment ............................................................................. 58
12.1 Human Health Screening........................................................................................ 58
Introduction ................................................................................................... 58 12.1.1
Conceptual Exposure Model ....................................................................... 58 12.1.2
12.1.2.1 Current/Future Recreational Fisherman .............................................. 60
12.1.2.2 Current/Future Recreational Swimmer ................................................ 60
12.1.2.3 Current/Future Recreational Hunter .................................................... 60
12.1.2.4 Current/Future Industrial Worker ........................................................ 60
12.1.2.5 Future Resident ........................................................................................ 60
Risk-Based Screening Levels ....................................................................... 60 12.1.3
Site Specific Risk Based Remediation Standards ..................................... 78 12.1.4
12.2 Ecological Screening ................................................................................................ 78
Introduction ........................................................................................................ 78 12.2.1
Ecological Setting ............................................................................................... 78 12.2.2
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12.2.2.1 Facility Site Summary ............................................................................. 78
12.2.2.2 Regional Ecological Setting .................................................................... 78
12.2.2.3 Description of Ecoregion and Expected Habitats ............................... 79
12.2.2.4 Watershed in which the Site is Located ............................................... 79
12.2.2.5 Average Rainfall ...................................................................................... 79
12.2.2.6 Average Temperature ............................................................................. 79
12.2.2.7 Length of Growing Season ..................................................................... 79
12.2.2.8 Threatened and Endangered Species that use Habitats in the
Ecoregion ................................................................................................................... 79
12.2.2.9 Site-Specific Ecological Setting .............................................................. 79
12.2.2.10 On-site and Off-site Land Use ............................................................. 79
12.2.2.11 Habitats within the Site Boundary ...................................................... 80
12.2.2.12 Description of Man-made Units that May Act as Habitat ............... 80
12.2.2.13 Site Layout and Topography ............................................................... 80
12.2.2.14 Surface Water Runoff Pathways ......................................................... 81
12.2.2.15 Soil Types................................................................................................ 81
12.2.2.16 Species Normally Expected to Use Site under Relatively Unaffected
Conditions ................................................................................................................. 81
12.2.2.17 Species of Special Concern ................................................................... 81
12.2.2.18 Nearby Critical and/or Sensitive Habitats ......................................... 81
Fate and Transport Mechanisms ...................................................................... 81 12.2.3
Preliminary Exposure Estimate and Risk Calculation.................................. 83 12.2.4
Comparison to Ecological Screening Levels .................................................. 83 12.2.5
12.3 Uncertainty and Data Gaps .................................................................................... 90
12.4 Scientific/Management Decision Point ................................................................. 90
12.5 Risk Assessment Summary..................................................................................... 91
13.0 Groundwater Modeling ............................................................................................... 92
13.1 Groundwater Modeling to be Performed in CAP ............................................... 92
13.2 Description of Kd Term Development.................................................................. 93
13.3 Description of Flow Transects ................................................................................ 93
13.4 Other Model Inputs ................................................................................................. 94
14.0 Data Gaps – Site Conceptual Model Uncertainties ................................................ 95
14.1 Data Gaps .................................................................................................................. 95
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14.2 Site Heterogeneities ................................................................................................. 95
14.3 Impact of Data Gaps and Site Heterogeneities .................................................... 96
15.0 Planned Sampling for CSA Supplement ................................................................. 97
16.0 Interim Groundwater Monitoring Plan .................................................................... 98
16.1 Sampling Frequency ................................................................................................ 98
16.2 Constituent and Parameter List ............................................................................. 98
16.3 Proposed Sampling Locations ................................................................................ 98
16.4 Proposed Background Wells .................................................................................. 98
17.0 Discussion ...................................................................................................................... 99
17.1 Maximum COI Concentrations .............................................................................. 99
17.2 Summary of Completed and Ongoing Work ..................................................... 100
17.3 Contaminant Migration and Potentially Affected Receptors .......................... 100
18.0 Conclusions and Recommendations ....................................................................... 101
18.1 Source and Cause of Contamination ................................................................... 101
18.2 Imminent Hazards to Public Health and Safety and Actions Taken to Mitigate
Them ........................................................................................................................ 101
18.3 Receptors and Significant Exposure Pathways ................................................. 101
18.4 Horizontal and Vertical Extent of Soil and Groundwater Contamination .... 102
18.5 Geological and Hydrogeological Features influencing the Movement,
Chemical, and Physical Character of the Contaminants .............................................. 104
18.6 Proposed Continued Monitoring......................................................................... 104
18.7 Preliminary Evaluation of Corrective Action Alternatives.............................. 104
19.0 References ..................................................................................................................... 106
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LIST OF FIGURES
Executive Summary
Figure ES-1 Site Conceptual Model - Plan View
1.0 Introduction
Figure 1-1 Site Location Map
Figure 1-2 Site Layout Map
2.0 Site History and Description
Figure 2-1 1949 Aerial Photograph
Figure 2-2 1981 Aerial Photograph
Figure 2-3 Historical USGS Topographic Map
3.0 Source Characteristics
Figure 3-1 Known Sample of Ash for Comparison
Figure 3-2 Elemental Composition for Bottom Ash, Fly Ash, Shale, and Volcanic Ash
Figure 3-3 Coal Ash TCLP Leachate Concentration Ranges Compared to Regulatory
Limits
Figure 3-4 Trace Element Concentration Ranges in Ash Compared to EPA
Residential Soil Screening Levels
6.0 Site Geology and Hydrogeology
Figure 6-1 Geologic Cross-Section A-A'
Figure 6-2 Geologic Cross-Section B-B' and C-C'
Figure 6-3 Geologic Cross-Section A-A' North End with Photographs
Figure 6-4 Geologic Cross-Section A-A' South End with Photographs
Figure 6-5 Geologic Cross-Section C-C' with Photographs
Figure 6-6 Potentiometric Surface - Upper Surficial Aquifer, June 1, 2015
Figure 6-7 Potentiometric Surface - Lower Surficial Aquifer, June 1, 2015
Figure 6-8 Potentiometric Surface - Pee Dee Aquifer, June 1, 2015
Figure 6-9 Cross Section - Site Conceptual Model
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LIST OF FIGURES
8.0 Soil and Rock Characterization
Figure 8-1 Geologic Cross-Section A-A' with COI Analytical Results
Figure 8-2 Geologic Cross-Sections B-B' and C-C' with COI Analytical Results
Figure 8-3 Site Map with Soil Exceedances
10.0 Groundwater Characterization
Figure 10-1 Site Layout with 2L Exceedances - Upper Surficial Aquifer
Figure 10-2 Site Layout with 2L Exceedances - Lower Surficial Aquifer
Figure 10-3 Site Layout with 2L Exceedances - Upper Pee Dee Wells
Figure 10-4 Site Layout with 2L Exceedances - Lower Pee Dee Wells
Figure 10-5 June 2015 Isoconcentration Map - Arsenic in Upper Surficial Wells
Figure 10-6 June 2015 Isoconcentration Map - Barium in Upper Surficial Wells
Figure 10-7 June 2015 Isoconcentration Map - Boron in Upper Surficial Wells
Figure 10-8 June 2015 Isoconcentration Map - Cobalt in Upper Surficial Wells
Figure 10-9 June 2015 Isoconcentration Map - Iron in Upper Surficial Wells
Figure 10-10 June 2015 Isoconcentration Map - Manganese in Upper Surficial Wells
Figure 10-11 June 2015 Isoconcentration Map - pH in Upper Surficial Wells
Figure 10-12 June 2015 Isoconcentration Map - Thallium in Upper Surficial Wells
Figure 10-13 June 2015 Isoconcentration Map - Total Dissolved Solids in Upper
Surficial Wells
Figure 10-14 June 2015 Isoconcentration Map - Vanadium in Upper Surficial Wells
Figure 10-15 June 2015 Isoconcentration Map - Arsenic in Lower Surficial Wells
Figure 10-16 June 2015 Isoconcentration Map - Barium in Lower Surficial Wells
Figure 10-17 June 2015 Isoconcentration Map - Boron in Lower Surficial Wells
Figure 10-18 June 2015 Isoconcentration Map - Cobalt in Lower Surficial Wells
Figure 10-19 June 2015 Isoconcentration Map - Iron in Lower Surficial Wells
Figure 10-20 June 2015 Isoconcentration Map - Manganese in Lower Surficial Wells
Figure 10-21 June 2015 Isoconcentration Map - pH in Lower Surficial Wells
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LIST OF FIGURES
10.0 Groundwater Characterization (Continued)
Figure 10-22 June 2015 Isoconcentration Map - Thallium in Lower Surficial Wells
Figure 10-23 June 2015 Isoconcentration Map - Total Dissolved Solids in Lower
Surficial Wells
Figure 10-24 June 2015 Isoconcentration Map - Vanadium in Lower Surficial Wells
Figure 10-25 June 2015 Isoconcentration Map - Arsenic in Upper Pee Dee Wells
Figure 10-26 June 2015 Isoconcentration Map - Barium in Upper Pee Dee Wells
Figure 10-27 June 2015 Isoconcentration Map - Boron in Upper Pee Dee Wells
Figure 10-28 June 2015 Isoconcentration Map - Cobalt in Upper Pee Dee Wells
Figure 10-29 June 2015 Isoconcentration Map - Iron in Upper Pee Dee Wells
Figure 10-30 June 2015 Isoconcentration Map - Manganese in Upper Pee Dee Wells
Figure 10-31 June 2015 Isoconcentration Map - pH in Upper Pee Dee Wells
Figure 10-32 June 2015 Isoconcentration Map - Thallium in Upper Pee Dee Wells
Figure 10-33 June 2015 Isoconcentration Map - Total Dissolved Solids in Upper Pee
Dee Wells
Figure 10-34 June 2015 Isoconcentration Map - Vanadium in Upper Pee Dee Wells
Figure 10-35 June 2015 Isoconcentration Map - Arsenic in Lower Pee Dee Wells
Figure 10-36 June 2015 Isoconcentration Map - Barium in Lower Pee Dee Wells
Figure 10-37 June 2015 Isoconcentration Map - Boron in Lower Pee Dee Wells
Figure 10-38 June 2015 Isoconcentration Map - Cobalt in Lower Pee Dee Wells
Figure 10-39 June 2015 Isoconcentration Map - Iron in Lower Pee Dee Wells
Figure 10-40 June 2015 Isoconcentration Map - Manganese in Lower Pee Dee Wells
Figure 10-41 June 2015 Isoconcentration Map - pH in Lower Pee Dee Wells
Figure 10-42 June 2015 Isoconcentration Map - Thallium in Lower Pee Dee Wells
Figure 10-43 June 2015 Isoconcentration Map - Total Dissolved Solids in Lower Pee
Dee Wells
Figure 10-44 June 2015 Isoconcentration Map - Vanadium in Lower Pee Dee Wells
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LIST OF FIGURES
10.0 Groundwater Characterization (Continued)
Figure 10-45 CCR Rule Detection Monitoring Constituent Map - Upper Surficial
Aquifer
Figure 10-46 CCR Rule Detection Monitoring Constituent Map - Lower Surficial
Aquifer
Figure 10-47 CCR Rule Detection Monitoring Constituent Map - Upper Pee Dee
Wells
Figure 10-48 CCR Rule Detection Monitoring Constituent Map - Lower Pee Dee
Wells
Figure 10-49 CCR Rule Assessment Monitoring Constituent Map - Upper Surficial
Aquifer
Figure 10-50 CCR Rule Assessment Monitoring Constituent Map - Lower Surficial
Aquifer
Figure 10-51 CCR Rule Assessment Monitoring Constituent Map - Upper Pee Dee
Wells
Figure 10-52 CCR Rule Assessment Monitoring Constituent Map - Lower Pee Dee
Wells
Figure 10-53 Ash Pore Water Piper Diagrams
Figure 10-54 Pee Dee Water Piper Diagrams
Figure 10-55 Surficial Aquifer (Shallow) Piper Diagrams
Figure 10-56 Surficial Aquifer (Intermediate) Piper Diagrams
Figure 10-57 Surficial Aquifer (Deep) Piper Diagrams
Figure 10-58 Surface Water Piper Diagram
Figure 10-59 Compliance Well Box and Whisker Plots - Arsenic, Barium, Boron
Figure 10-60 Compliance Well Box and Whisker Plots - Chloride, Iron, Manganese
Figure 10-61 Compliance Well Box and Whisker Plots - Nitrate, Selenium, Sulfate
Figure 10-62 Compliance Well Box and Whisker Plots - TDS, Thallium, Zinc
Figure 10-63 Compliance Well Box and Whisker Plots - Dissolved Oxygen, pH,
Turbidity
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LIST OF FIGURES
11.0 Hydrogeological Investigation
Figure 11-1 Geologic Cross-Sections with Boron and Arsenic
Figure 11-2 Geologic Cross-Sections with Iron and Cobalt
Figure 11-3 Geologic Cross-Sections with Manganese and Vanadium
Figure 11-4 Geologic Cross-Sections with Thallium
12.0 Screening-Level Risk Assessment
Figure 12-1 Conceptual Exposure Model - Human Health
Figure 12-2 COPC Locations Flagged - Groundwater - Ash Pore Water - Human
Health
Figure 12-3 COPC Locations Flagged - Groundwater - Upper Surficial Aquifer -
Human Health
Figure 12-4 COPC Locations Flagged - Groundwater - Lower Surficial Aquifer -
Human Health
Figure 12-5 COPC Locations Flagged - Groundwater - Upper Pee Dee Aquifer -
Human Health
Figure 12-6 COPC Locations Flagged - Groundwater - Lower Pee Dee Aquifer -
Human Health
Figure 12-7 COPC Locations Flagged - Soils (0-2 feet) - Human Health
Figure 12-8 COPC Locations Flagged - Sediment - Human Health
Figure 12-9 COPC Locations Flagged - Surface Water - Human Health
Figure 12-10 Conceptual Exposure Model - Ecological CEM
Figure 12-11 COPC Locations Flagged - Soils (0-2 feet) - Ecological
Figure 12-13 COPC Locations Flagged - Sediment - Ecological
Figure 12-12 COPC Locations Flagged - Surface Water - Ecological
16.0 Interim Groundwater Monitoring Plan
Figure 16-1 Proposed Groundwater Monitoring Locations
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LIST OF TABLES
2.0 Site History and Description
Table 2-1 NPDES Groundwater Monitoring Requirements
Table 2-2 Compliance Well 15 NCAC 2L Exceedances
3.0 Source Characteristics
Table 3-1 Ash, Rock, and Soil Composition
6.0 Site Geology and Hydrogeology
Table 6-1 Exploration and Sampling Plan
Table 6-2 Soil, Sediment, and Ash COIs and Analytical Methods
Table 6-3 Ash Pore Water, Groundwater, and Surface Water COIs Analytical Methods
Table 6-4 Well Construction Data
Table 6-5 Water Level Measurements - June 2015
Table 6-6 Local Groundwater Gradients and Flow Velocities
Table 6-7 In-Situ Hydraulic Conductivity Test Results
Table 6-8 Vertical Hydraulic Conductivity of Undisturbed Soil Samples
7.0 Source Characterization
Table 7-1 Physical Properties of Ash
Table 7-2 Mineralogy of Ash
Table 7-3 Chemical Properties of Ash
Table 7-4 Leaching Properties of Ash
Table 7-5 Whole Rock Metal Oxide Analysis of Ash
Table 7-6 Whole Rock Elemental Analysis of Ash
Table 7-7 Ash Pore Water Analytical Results
Table 7-8 2015 15 NCAC 2L Exceedances in Ash Pore Water
Table 7-9 Valence Speciation of Ash Pore Water
8.0 Soil and Rock Characterization
Table 8-1 Physical Properties of Soil
Table 8-2 Mineralogy of Soils
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Table 8-3 Chemical Properties of Soil
Table 8-4 Leaching Properties of Soil
Table 8-5 Whole Rock Metal Oxide Analysis of Soil
Table 8-6 Whole Rock Elemental Analysis of Soil
9.0 Sediment, Seep, and Surface Water Characterization
Table 9-1 Sediment Analytical Results
Table 9-2 Surface Water Analytical Results
Table 9-3 15 NCAC 2B Exceedances in Surface Water
10.0 Groundwater Characterization
Table 10-1 Groundwater Analytical Results
Table 10-2 15 NCAC 2L Exceedances in Groundwater
Table 10-3 Valence Speciation of Groundwater
Table 10-4 Radiological Analytical Results
Table 10-5 Cations-Anions Balance
12.0 Screening-Level Risk Assessment
Table 12-1 Risk Screening Table: Coal Ash Pore Water Data
Table 12-2 Coal Ash COPC Determination
Table 12-3 Risk Screening Table: Surficial Aquifer Background Groundwater Data
Table 12-4 Risk Screening Table: Surficial Aquifer Downgradient Groundwater Data
Table 12-5 Risk Screening Table: Pee Dee Formation Groundwater Data
Table 12-6 Soils (0-2) Analytical Results with Screening Criteria - Residential and
Industrial Soils - Human Health
Table 12-7 Sediment Analytical Results with Screening Criteria - Residential and
Industrial Soils - Human Health
Table 12-8 Surface Water Analytical Results with Screening Criteria - EPA
Recommended Water Quality Criteria and NCAC 2B Standards -
Human Health
Table 12-9 Matrix for Determination of Constituents of Potential Concern - Human
Health
Table 12-10 Threatened & Endangered Species in New Hanover County
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Table 12-11 Surface Water Analytical Results with Screening Criteria - NCAC 2B and
EPA Recommended Water Quality Criteria for Aquatic Life (Acute and
Chronic) - Ecological
Table 12-12 Soils (0-2) Analytical Results - EPA Ecological Soil Screening Levels and
EPA Region 4 Recommended Ecological Screening Values for Soil
Table 12-13 Sediment Analytical Results with Screening Criteria - EPA Region 4 Soil
Screening Levels and EPA Region 4 Recommended Ecological Screening
Values - Ecological
Table 12-14 Matrix for Determination of Constituents of Potential Concern -
Ecological
16.0 Interim Groundwater Monitoring Plan
Table 16-1 Recommended Groundwater Monitoring Parameters
Table 16-2 Recommended Groundwater Monitoring Locations
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LIST OF APPENDICES
Appendix A Regulatory Correspondence
NCDENR to DEP, 7/7/2015
NCDENR to DEP, 6/9/2015
NCDENR CSA Guideline Adjustment, Final Addendum 1, June 2015
NCDENR to DEP, 5/22/2015
NCDENR to DEP, 2/6/2015
NCDENR to DEP, 11/4/2014
NCDENR to DEP, 8/13/2014
NCDENR Hydrogeologic Investigation and Reporting Policy
Appendix B Water Well and Receptor Survey
Table B-1 NCDENR 2015 Water Well Data
Table B-2 NCDENR Water Supply Well Tracking Information
Table B-3 Public and Private Water Supply Wells (0.5 Mile Radius)
Table B-4 Parcel Ownership Information
Figure B-1 Receptor Vicinity Map
NCDENR 2015 Water Well Sample Laboratory Results and Chain of Custody
Forms (CD)
Appendix C Methodology
SynTerra Field Procedures
Appendix D Quality Control Data
Table D-1 Rinse Blank Analyses for Soils
Table D-2 Rinse Blank Analyses for Groundwater -TOTAL
Table D-3 Rinse Blank Analyses for Groundwater -DISSOLVED
Appendix E 2015 Groundwater Assessment Documentation
Boring Logs and Well Construction Diagrams
Driller Well Construction Records
Historical Boring Logs and Well Construction Diagrams
Appendix F Soils Test Data
Whole Rock Metal Oxides, Whole Rock Elemental Analysis,
X-ray Diffraction
Grain Size Distribution and Specific Gravity
Moisture Content
Vertical Hydraulic Conductivity
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LIST OF APPENDICES
Appendix G In-Situ Hydraulic Conductivity Measurements
Slug Test Results
Appendix H Statistical Analysis of Compliance Well Groundwater Results
Table 1 Summary of Percent Nondetects, Treatment Type, and Data Distribution
- March 2015
Table 2 Summary of Interwell Prediction Limit Results – March 2015
Figure H-1 Time versus Concentration - Comparison Between Compliance &
Background Wells - Barium
Figure H-2 Time versus Concentration - Comparison Between Compliance &
Background - Boron
Figure H-3 Time versus Concentration - Comparison Between Compliance &
Background - Chloride
Figure H-4 Time versus Concentration - Comparison Between Compliance &
Background - Iron
Figure H-5 Time versus Concentration - Comparison Between Compliance &
Background - Manganese
Figure H-6 Time versus Concentration - Comparison Between Compliance &
Background - Sulfate
Figure H-7 Time versus Concentration - Comparison Between Compliance &
Background - TDS
Figure H-8 Time versus Concentration and ORP MW-4B, MW-22B, MW-23B
Figure H-9 Time versus Concentration and ORP MW-24B, MW-27B, MW-28B
Figure H-10 Time versus Concentration and ORP MW-5C, MW-7C, MW-21C
Figure H-11 Time versus Concentration and ORP MW-22C, MW-23C, MW-24C
Figure H-12 Time versus Concentration and ORP-MW-28C, MW-31C
Figure H-13 Time versus Concentration and ORP-MW-11, MW-12, MW 19
Appendix I Screening Level Risk Assessment
Ecological Assessment Checklist
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LIST OF ATTACHMENTS
Attachment 1 Historical Geosyntec Reports
Attachment 2 Topographic, Underground Utility Maps, and EDR Reports (CD)
Attachment 3 Drinking Water and Receptor Survey Reports (CD)
Attachment 4 Comprehensive Analytical Results Table (CD)
Attachment 5 Laboratory Reports - Chemical Analyses (CD)
Attachment 6 Photographs (CD)
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LIST OF ACRONYMS
AMSL above mean sea level
ARAR Applicable or Relevant and Appropriate Requirements
ASTM American Society for Testing and Materials
BBL
BW
Blasland, Bouck and Lee
Background Well
bgs below ground surface
CAMA Coal Ash Management Act
CCR Coal Combustion Residuals
CEM Conceptual Exposure Model
CFPUA
COI
Cape Fear Public Utility Authority
Constituents of Interest
COPC Constituents of Potential Concern
CPT
CSA
Cone Penetrometer Test
Comprehensive Site Assessment
CUB
DEP
Confining Unit Boring
Duke Energy Progress, Inc.
DO Dissolved Oxygen
DPT Direct Push Technology
DWR Division of Water Resources
EDXRF Energy Dispersive X-ray Diffraction
ESV Ecological Screening Value
FADA
GAP
Former Ash Disposal Area
Groundwater Assessment Plan
GIS Geographic Information System
HHRA Human Health Risk Assessment
HQ
IMAC
Hazard Quotient
Interim Maximum Allowable Concentration
MCL Maximum Contaminant Level
MSL Mean Sea Level
MW Monitoring Well
NCDENR North Carolina Department of Environment and Natural Resources
NOAA National Oceanic and Atmospheric Administration
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LIST OF ACRONYMS
NORR Notice of Regulatory Requirements
NPDES National Pollution Discharge Elimination System
NTU Nepthalic Turbidity Unit
NURE
ORP
National Uranium Resource Evaluation
Oxidation-Reduction Potential
OW Observation Well
PVC Polyvinylchloride
PZ Piezometer
RSL USEPA Regional Screening Level
SCM
Site
Site Conceptual Model
L.V. Sutton Energy Complex
SLERA Screening Level Ecological Risk Assessment
SPLP Synthetic Precipitation Leaching Procedure
SW Surface Water
2B NCDENR/DWR Title 15, Subchapter 2B. Surface Water and
Wetland Standards
2L NCDENR/DWR Title 15, Subchapter 2L. Groundwater Quality
Standards
TDS Total Dissolved Solids
TOC Total Organic Carbon
USACE US Army Corps of Engineers
USEPA United States Environmental Protection Agency
USGS United States Geological Survey
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1.0 INTRODUCTION
Duke Energy Progress, Inc. (Duke Energy) owns and operates the L.V. Sutton Energy
Complex (Site) located on approximately 3,300 acres near Wilmington, North Carolina.
The Site is located along the east bank of the Cape Fear River northwest of Wilmington
and west of US Highway 421. The Site location is shown on Figure 1-1.
The Site started operations in 1954 with three coal-fired boilers that primarily used
bituminous coal as fuel to produce steam to generate electricity. Ash generated from
coal combustion was originally stored on-site in the 'former ash disposal area (FADA)',
also known as the ‘lay of land area’ , then in the 1971 ash basin (old ash basin), and
finally the 1984 ash basin (new ash basin) (Figure 1-2). These ash storage areas are
referred to as the ash management area. The Site ceased burning coal in November
2013 and switched to natural gas for electricity generation, thus the facility no longer
generates coal ash.
Discharges from the cooling pond and the ash basins are permitted by the North
Carolina Department of Environment and Natural Resources (NCDENR) Division of
Water Resources (DWR) under the National Pollution Discharge Elimination System
(NPDES) Permit NC0001422. Duke Energy has performed groundwater monitoring
under the NPDES permit since 1990. The current groundwater compliance monitor
wells required for the NPDES permit are sampled three times a year and the analytical
results are submitted to the DWR. Groundwater compliance monitoring is performed
in addition to the normal NPDES monitoring of the discharge flows.
Concentrations of arsenic, barium, boron, iron, manganese, thallium, vanadium, and
total dissolved solids (TDS) in excess of North Carolina Administrative Code (NCAC)
Title 15A Chapter 02L.0202 groundwater quality standards (2L) or the Interim
Maximum Allowable Concentration (IMAC) have been measured in groundwater
samples collected in ash pore water wells. These constituents are considered
constituents of interest (COI) for this assessment. Concentrations of cobalt and
selenium in excess of the 2L or IMAC have been measured in groundwater samples
collected at compliance monitor wells. Since cobalt and selenium were not detected in
the ash pore wells, they are not considered COIs.
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1.1 Purpose of Comprehensive Site Assessment
The Comprehensive Site Assessment (CSA) was conducted to collect information
necessary to understand the ash basin as a source of potential impact, the vertical and
horizontal extent of COIs, identify potential receptors of constituents, evaluate risks to
receptors, and ultimately develop a Corrective Action Plan (CAP).
A Site Conceptual Model (SCM) and associated physical properties and chemical data
are to be used as the basis for a groundwater flow model and an associated COI fate
and transport model for the ash basin. Some of the COIs are present in upgradient
groundwater and these will be discussed later in this document. The subsequent CAP
for the Site is to be based on the results of risk assessments and groundwater models.
1.2 Regulatory Background
In a Notice of Regulatory Requirements (NORR) dated August 13, 2014, DWR
requested that Duke Energy prepare a Groundwater Assessment Plan to conduct a CSA
in accordance with 15A NCAC 02L .0106(g) to address groundwater constituent
concentrations detected above 2L groundwater quality standards at the compliance
boundary.
NCDENR Requirements 1.2.1
NCDENR issued site specific requirements for the Site in letters dated November
4, 2014 and February 6, 2015. Specific NCDENR requirements for the CSA
attached to the February letter were modified after issuance of the letter and
were finalized in June 2015.
NORR Requirements 1.2.2
The NORR required Duke Energy to comply with 15A NCAC 02L .0106(g),
DWR’s Groundwater Modeling Policy, May 31, 2007, and various site specific
requirements.
Coal Ash Management Act Requirements 1.2.3
In addition, the Coal Ash Management Act (CAMA) 2014 – General Assembly of
North Carolina Senate Bill 729 Ratified Bill (Session 2013) (SB 729) revised North
Carolina General Statute 130A-309.209(a) require the following:
(a) Groundwater Assessment of Coal Combustion Residuals Surface Impoundments.
– The owner of a coal combustion residuals surface impoundment shall conduct
groundwater monitoring and assessment as provided in this subsection. The
requirements for groundwater monitoring and assessment set out in this subsection are
in addition to any other groundwater monitoring and assessment requirements
applicable to the owners of coal combustion residuals surface impoundments.
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(1) No later than December 31, 2014, the owner of a coal combustion residuals
surface impoundment shall submit a proposed Groundwater Assessment Plan for
the impoundment to the Department for its review and approval. The
Groundwater Assessment Plan shall, at a minimum, provide for all of the
following:
a. A description of all receptors and significant exposure pathways.
b. An assessment of the horizontal and vertical extent of soil and
groundwater contamination for all contaminants confirmed to be present
in groundwater in exceedance of groundwater quality standards.
c. A description of all significant factors affecting movement and transport
of contaminants.
d. A description of the geological and hydrogeological features influencing
the chemical and physical character of the contaminants.
e. A schedule for continued groundwater monitoring.
f. Any other information related to groundwater assessment required by the
Department.
(2) The Department shall approve the Groundwater Assessment Plan if it determines
that the Plan complies with the requirements of this subsection and will be
sufficient to protect public health, safety, and welfare; the environment; and
natural resources.
(3) No later than 10 days from approval of the Groundwater Assessment Plan, the
owner shall begin implementation of the Plan.
(4) No later than 180 days from approval of the Groundwater Assessment Plan, the
owner shall submit a Groundwater Assessment Report to the Department. The
Report shall describe all exceedances of groundwater quality standards associated
with the impoundment.
1.3 NCDENR-Duke Energy Correspondence
On behalf of Duke Energy, SynTerra submitted to NCDENR a proposed Groundwater
Assessment Plan (GAP) for the Site dated September 2014. Subsequently, NCDENR
issued a comment letter dated November 4, 2014 containing both general comments
applicable to the Duke Energy ash basin facilities and site-specific comments for the Site
(Appendix A). In response to these comments, SynTerra prepared and submitted a
revised Groundwater Assessment Work Plan (Revision 1) on December 30, 2014, for
performing the groundwater assessment as prescribed in the NORR and SB 729, and to
address the NCDENR review of the Work Plan dated November 4, 2014 and
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subsequent meetings among Duke Energy, SynTerra, and NCDENR. Conditional
approval of the Work Plan was dated February 6, 2015 (Appendix A).
1.4 Approach to Comprehensive Site Assessment
The approach to the CSA was developed to meet NCDENR’s requirements.
NORR Guidance 1.4.1
This CSA was conducted in accordance with the conditionally approved Work
Plan to meet the requirements of 15A NCAC 02L .0106(g). This rule requires:
(g) The Site assessment conducted pursuant to the requirements of
Paragraph (c) of this Rule, shall include:
(1) The source and cause of contamination;
(2) Any imminent hazards to public health and safety and actions taken
to mitigate them in accordance with Paragraph (f) of this Rule;
(3) All receptors and significant exposure pathways;
(4) The horizontal and vertical extent of soil and groundwater
contamination and all significant factors affecting contaminant
transport; and
(5) Geological and hydrogeological features influencing the movement, chemical, and
physical character of the contaminants.
USEPA Monitored Natural Attenuation Tiered Approach 1.4.2
The assessment data is also compiled in a manner to be consistent with
“Monitored Natural Attenuation of Inorganic Contaminants in Groundwater”
(EPA/600/R-07/139). The tiered analysis approach discussed in this guidance
document is designed to align site characterization tasks to reduce uncertainty in
remedy selection. The tiered assessment data collection includes information to:
1. Evaluate active contaminant removal from ground water and dissolved
plume stability,
2. Evaluate the mechanisms and rates of attenuation,
3. Evaluate the long-term capacity for attenuation and stability of immobilized
contaminants, and
4. Evaluate anticipated performance monitoring needs to support the selected
remedy.
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This assessment information will be used to develop a CAP for the Site. The
CAP will provide a demonstration of these in support of the recommended Site
remedy.
ASTM Conceptual Site Model 1.4.3
The American Society for Testing and Materials (ASTM) E1689-95(2014)
generally describes the major components of conceptual site models, including
an outline for developing models. To the extent possible, this guidance was
incorporated into preparation of the SCM.
1.5 Technical Objectives
The rationale for borings and wells installed and sampled during the assessment fall
into one of the following categories:
Determine the range of background groundwater quality from pertinent geologic
settings (horizontal and vertical) across a broader area of the Site and a greater
distance from the ash basins.
Evaluate groundwater quality from pertinent geologic settings (horizontal and
vertical extent of coal ash leachate constituents) at a greater distance down
gradient of the ash basins than previously available.
Establish perimeter (horizontal and vertical) boundary conditions for a
groundwater modeling.
Provide source area information including pore water chemistry, physical and
hydraulic properties, coal ash thickness and residual saturation within the ash
basins.
Address soil chemistry data gaps in the vicinity of the ash basins & FADA
(horizontal and vertical extent of coal ash leachate constituents in soil) and a
comparison to background concentrations.
Determine potential routes of exposure and receptors.
The following report presents the information obtained from the field investigation to
address the requirements of 15A NCAC 02L .0106(g), the conditional approval letter,
and CSA guidance document (revised June 2015).
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2.0 SITE HISTORY AND DESCRIPTION
An overview of the Site setting and operations is presented in the following sections.
2.1 Site Location, Acreage, and Ownership
The Site is a former coal-fired electrical power generation facility located on
approximately 3,300 acres near the City of Wilmington in New Hanover County (Figure
1-1). Duke Energy Progress, Inc. owns the Site. Records available from Environmental
Data Resources, Inc. (Attachment 2) do not contain any information prior to
construction of the Site.
2.2 Plant Description
The Site started operations in 1954 and consisted of three coal-fired boilers that
primarily used bituminous coal as fuel to produce steam. Ash generated from coal
combustion was first stored on-site in the FADA; beginning in 1971 ash was stored in
the ‘old ash basin’ and then in 1984 the ‘new ash basin’ (Figure 1-2). These ash storage
areas are referred to as the ash management area.
The Plant, cooling pond (Lake Sutton) and ash management area are located on the east
side of the Cape Fear River. The ash management area is located adjacent to the cooling
pond, north of the Plant, as shown on Figure 1-2. The ash management area consists of
three locations (Duke Energy, October 31, 2014):
The FADA, also known as the lay of land area is located south of the ash basins,
on the south side of the canal. It is believed that ash may have been placed in
this area between approximately 1954 and 1972.
The 1971 ash basin (old ash basin) is an unlined ash basin built in approximately
1971. The basin contains fly ash, bottom ash, boiler slag, storm water, ash sluice
water, coal pile runoff, and low volume wastewater.
An ash basin with a 12-inch thick clay liner was built in approximately 1984 (new
ash basin), located toward the northern portion of the ash management area, and
was operated from 1984 to 2013. The basin contains fly ash, bottom ash, boiler
slag, storm water, ash sluice water, coal pile runoff, and low volume wastewater.
During coal sluicing operations, water was discharged from the 1971 and 1984 ash
basins to the cooling pond under the NPDES permit. Historical aerial photographs of
the Site from 1949 and 1981 are presented as Figures 2-1 and 2-2. The 1971 and 1984 ash
basins are impounded by an earthen dike. A USGS topographic map (composite from
1944 – 1954 maps) of the Site indicates that the property was undeveloped rural land at
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that time (Figure 2-3). According to Duke Energy (Duke Energy, October 31, 2014) the
old and new ash basins contain approximately 6,320,000 tons of ash and the FADA area
contains approximately 840,000 tons of ash. No other types of waste other than NPDES
permitted waste are believed to have been placed in the basins or FADA.
Coal ash, a potential source of impact at the Site, is no longer generated at the Site.
Duke Energy will fully excavate the ash basins with the material to be safely recycled or
reused in a lined structural fill or place in a lined landfill as required by CAMA.
2.3 General Site Description
The Site consists of approximately 3,300 acres and is developed with the power plant
structures, the ash basins, cooling pond and associated canals. The plant structures are
located primarily in the south central portion of the Site with the ash basins north of
these structures. Plant water production wells are located along the entrance road on
the east side of the Site (Figure 1-2). The northern and southern portions of the Site are
primarily undeveloped areas containing small sand hills, pine woods and brush.
The Site utilizes an approximate 1,100-acre cooling pond, referred to as Lake Sutton,
located adjacent to the Cape Fear River. A boat ramp and parking lot are located at the
north end of the lake; this feature is accessed by way of Sutton Lake Road, which
extends across the Site from NC Hwy 421 to Lake Sutton.
2.4 Adjacent Property, Zoning, and Surrounding Land Uses
The Site is surrounded by commercial, industrial, mining (sand quarry), residential and
forest land. The quarry property and a plant located north of the quarry operate
production wells on land adjacent to the Site. No future change in use of the
surrounding land is currently anticipated.
2.5 Adjacent Surface Water Bodies and Classifications
The Cape Fear River, borders the Site immediately to the west. The Cape Fear River
flows south toward the town of Wilmington and is tidally influenced. NCDENR
classifies the Cape Fear River as “C;Sw” (Aquatic Life, Secondary Recreation,
Fresh/Swamp water).
2.6 Meteorological Setting
The Site lies within the southeastern United States coastal plain climate zone that
exhibits a humid subtropical climate type (NOAA, 2013). The high rainfall amounts
and substantial seasonal temperature variations in this region promote rapid
weathering of surficial geologic formations.
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2.7 Hydrologic Setting
Topography fluctuates from approximately 45 feet above mean sea level (MSL) at the
top of the 1971 ash basin to the water level along the Cape Fear River shoreline along
the west and southwest Site boundaries. Outside of the ash basin, natural topography
varies from 30 MSL among the small isolated sand hills in undeveloped portions of the
Site, to 10 feet MSL in the Site area and the FADA to the southeast. The Site plant,
cooling pond, and ash basins are located on the east side of the Cape Fear River, which
flows south and is tidally influenced.
2.8 Permitted Activities and Permitted Waste
The ash management areas, operated under NPDES Permit NC0001422, are located
along the east side of the cooling pond (north of the plant, shown with a 500 foot
compliance boundary on Figure 1-2). The permit authorizes the discharge of cooling
pond blowdown, recirculation cooling water, non-contact cooling water and treated
wastewater from Internal Outfalls 002, 003 and 004 via Outfall 001 from the cooling
pond to the Cape Fear River. The cooling pond outfall discharges to the Cape Fear
River via permitted Outfall 001. Internal outfalls 005 and 006 are discussed below.
2.9 History of NPDES and Surface Water Monitoring
The NPDES program regulates wastewater discharges to surface waters to ensure that
surface water quality standards are maintained. The Site operates under NPDES Permit
NC0001422 (effective January 1, 2012) which authorizes discharge of cooling pond
blowdown, recirculated cooling water, noncontact cooling water, and treated
wastewater from internal Outfalls 002, 003, and 004 (via external Outfall 001); coal pile
runoff, low volume wastes, ash sluice water (including wastewater generated from the
Rotomix system), and storm water runoff (Outfall 002); chemical metal cleaning waste
(Outfall 003); and ash sluice water (including wastewater generated from the Rotomix
system), coal pile runoff, low volume wastes, and storm water runoff (Outfall 004).
With the operation of the natural gas fired combined cycle generation facility, the Site
also discharges from internal Outfall 005 (ultrafilter water treatment system filter
backwash, Closed Cooling Water Cooler blowdown, Reverse Osmosis/
Electrodeionization system reject wastewater, and other Low Volume wastewater) to
the Cooling Pond. The Site also discharges from internal Outfall 006 (Low Volume
wastewater including the Heat Recovery Steam Generator blowdown and auxiliary
boiler blowdown). NPDES permits require renewal every 5 years.
In addition to surface water monitoring, the NPDES permit requires groundwater
monitoring. For purposes of this monitoring, the applicable groundwater reference is
the Groundwater Quality Standard 2L or former Interim Maximum Allowable
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Concentration (IMAC)) referenced in 15A NCAC 02L.0202. Appendix #1 of 15A NCAC
Subchapter 02L Classifications and Water Quality Standards Applicable to The Groundwaters
of North Carolina, lists 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.
The current groundwater monitoring plan for the Site includes the sampling of 17 wells.
Two additional wells have been added to the routine sampling on a voluntary basis
since November 2013. The sampling plan for the groundwater monitoring is presented
in Table 2-1.
Duke Energy has performed groundwater monitoring under the NPDES permit since
1990. The current compliance groundwater monitor wells required for the NPDES
permit are sampled three times a year and the analytical results are submitted to the
DWR. The compliance groundwater monitoring is performed in addition to the normal
NPDES monitoring of the discharge flows.
2.10 Assessment Activities or Previous Site Investigations
In addition to the required groundwater monitoring associated with permit activities,
additional sampling activities have been conducted at the Site since the late 1980s. Due
to the number of previous activities conducted at Site, only the most recent are
discussed here, with the exception of the FADA.
Existing monitor wells were installed by Blasland, Bouck & Lee (2004-2005),
Catlin Engineers and Scientists (2011), and SynTerra (2013). Existing piezometers were
installed by Golder Associates (2008). Monitoring wells were also installed in 1984,
1986, and 1990, but either well logs were not available for these wells or well logs did
not specify the entity who installed the wells.
In 2003, Carolina Power and Light signed an Administrative Order with the NC
Superfund Section Inactive Hazardous Sites Branch to voluntarily remediate the FADA
under the Registered Environmental Consultant Program (effective December 30, 2003).
Subsequent investigations included a Phase I Remedial Investigation completed by
Blasland, Bouck, & Lee, Inc. (BBL) in September 2004, and a Phase II Remedial
Investigation completed by BBL in May 2006, a Remedial Action Plan completed by
BBL in March 2006 and a Remedial Action Plan Addendum completed by BBL in
February 2007. In August 2007, Progress Energy submitted a letter to NCDENR,
Division of Water Management, terminating the Administrative Agreement for the Site.
The Administrative Agreement termination was accepted and the FADA ash storage
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area transferred from the Responsible Party Voluntary Remedial Action category to the
Sites Priority List category of the Inactive Hazardous Sites Inventory.
Catlin Engineers and Scientists (Catlin) conducted Phase I groundwater assessment
activities and selected suitable locations for placement of monitor wells for a Phase II
Work Plan (January 15, 2010). These assessments addressed a broader area of the Site
than did the previous Phase I/Phase II assessments completed by BBL. Sampling of
seven existing wells/piezometers was also included in the Phase I assessment scope of
work.
The results from the Phase I assessment did not detect arsenic, selenium, or sulfate at
concentrations greater than the 2L Standard in any of the groundwater samples
collected. Boron, iron, and manganese were detected at concentrations greater than the
2L Standard at one or more of the monitor wells and piezometers. However, as
reported in the Phase I report (February 11, 2011), shallow groundwater (“A” zone
wells/piezometers) was generally not impacted by COIs.
Based on the results of the Phase I report, a Phase II Work Plan was prepared and
submitted to NCDENR for approval. The Work Plan proposed targeting intermediate
and deeper zones and also included a telescoping well (MW-28T) to investigate the
potential presence of a confining clay and to collect a discrete deeper well sample.
Further, the Phase II Work Plan included two (2) temporary leachate characterization
collection points within the ash basin to obtain field scale data on ash basin leachate
composition.
The Phase II work consisted of installing 13 new monitor wells, two temporary leachate
collection points, and soil samples from each monitoring well boring for laboratory
analysis, groundwater gauging, slug testing, and two groundwater sampling events.
The results from the Phase II work indicated that arsenic was not detected above 2L in
any of the new wells. Boron was detected above the 2L in 8 of the 18 Phase II monitor
wells sampled, primarily in the deeper wells. Iron was detected above 2L in 10 of the 18
Phase II sampled monitor wells. Manganese was detected in all the Phase II
groundwater samples above 2L with the exception of samples collected from wells
MW-16 and MW-28T. Only two monitor wells (MW-24B and MW-27B,
September/October 2011 and January 2012 sampling events) indicated selenium
concentrations greater than 2L. Duke has continued with ongoing compliance well
monitoring and reporting of results to NCDENR.
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As part of Duke Energy’s ongoing plans to address closure options for the ash basin at
the Site, Geosyntec Consultants (Geosyntec) conducted assessment activities to develop
a conceptual closure plan for the Site ash management area. The assessment activities
included both hydrogeologic and environmental assessment activities and geotechnical
investigations of subsurface conditions within the ash management area. The
environmental activities included:
Installation of eight groundwater piezometers (four shallow and four
intermediate-depth) near the toe of the basin dikes. Installation of two pore
water piezometers within the ash basins. Installation of three intermediate-
depth and four deep groundwater monitor wells outside of the ash basins to
evaluate water levels and potential impacts to groundwater in the surficial
aquifer at the Site;
Four staff gauges were installed at certain surface water locations to facilitate
monitoring of surface water elevations;
Soil samples from background locations, from ash within the basins, from
native soil below the ash in the basins, and from monitoring well borings
located around the ash basins were collected and analyzed for COIs;
Groundwater and ash pore water samples were collected and analyzed for
select chemical constituents from the newly installed and certain non-
compliance monitor wells and piezometers located throughout the Site; and
Aquifer performance testing was conducted within one ash piezometer to
obtain an estimate of the hydraulic conductivity within the ash basins, and
five groundwater monitor wells were monitored with pressure transducers
to evaluate water level fluctuations.
The activities associated with the geotechnical investigation included;
Completion of 11 soil test borings (six through the perimeter dikes, three
within the ash basins and two within an area evaluated for a potential on-
site landfill);
14 Cone Penetration Test (CPT) soundings (including six seismic CPT)
soundings) and six direct push borings (DP);
Pore water dissipation tests were performed at nine selected CPT and
seismic CPT locations;
Two piezometers were installed, one within the 1971 basin and one within
the 1984 ash basin; and
Standard geotechnical laboratory tests were performed on collected soil and
ash field samples.
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No seeps have been identified at the Site. However, NCDENR and Duke Energy
collected split samples from the intake canal of the cooling pond and the discharge
canal to the cooling pond on March 10, 2014. The samples were analyzed for select
anions, metals, and TDS.
2.11 Corrective Actions
A Groundwater Mitigation and Monitoring Plan (Plan) was submitted to NCDENR on
July 9th, 2015, as required by the NORR dated June 9, 2015 in response to results of
receptor sampling and analyses. The Plan includes the installation of groundwater
extraction wells along the eastern Site boundary.
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3.0 SOURCE CHARACTERISTICS
The following overview of coal ash was prepared by HDR, Incorporated and supplied
for this report.
3.1 Coal Combustion and Ash Handling System
Coal ash is produced from the combustion of coal. The coal is dried, pulverized, and
conveyed to the burner area of a boiler. The smaller particles produced by coal
combustion, referred to as fly ash, are carried upward in the flue gas and are captured
by an air pollution control device, such as an electrostatic precipitator. The larger
particles of ash that fall to the bottom of the boiler are referred to as bottom ash or boiler
slag.
3.2 Physical Properties of Ash
Coal ash consists of fly ash and bottom ash produced from the combustion of coal. The
physical and chemical properties of coal ash are determined by reactions that occur
during the combustion of the coal and subsequent cooling of the flue gas. In general,
coal is dried, pulverized, and conveyed to the burner area of a boiler for combustion.
As described in Section 3.1, material that forms larger particles of ash and falls to the
bottom of the boiler is referred to as bottom ash or boiler slag. Smaller particles of ash,
known as fly ash, are carried upward in the flue gas and are captured by an air
pollution control device.
Approximately 70 to 80 percent of the ash produced during coal combustion is fly ash
(EPRI 1993). Typically 65 to 90 percent of fly ash has particle sizes that are less than
0.010 millimeter (mm). In general, fly ash has a grain size distribution similar to that of
silt. The remaining 20 to 30 percent of ash produced is considered to be bottom ash.
Bottom ash consists of angular particles with a porous surface and is normally gray to
black in color. Bottom ash particle diameters can vary from approximately 38 to 0.05
mm. In general, bottom ash has a grain size distribution similar to that of fine gravel to
medium sand (EPRI 1995).
Specific gravities of fly ash range from 2.1 to 2.9. The specific gravities of bottom ash
typically range from 2.3 to 3.0. The permeability of fly ash and bottom ash vary based
on material density, but would be within the range of a soil with a similar gradation
and density (EPRI 1995). Permeability and other physical properties of the ash found in
the RBSS ash basin are presented later in this report.
3.3 Chemical Properties of Ash
The specific mineralogy of coal ash varies based on many factors including the chemical
composition of the coal, which is directly related to the geographic region where the
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coal was mined, the type of boiler where the combustion occurs (i.e., thermodynamics
of the boiler), and air pollution control technologies employed.
The overall chemical composition of coal ash resembles that of siliceous rocks from
which it was derived, particularly shale. Oxides of silicon, aluminum, iron, and calcium
make up more than 90 percent of most siliceous rocks, soils, fly ash, and bottom ash.
Other major and minor elements (sulfur, sodium, potassium, magnesium, titanium)
make up an additional 8 percent, while trace constituents account for less than 1
percent. The following constituents are considered to be trace elements: arsenic, barium,
cadmium, chromium, lead, mercury, selenium, copper, manganese, nickel, lead,
vanadium, and zinc (EPRI 2010).
Duke Energy has typically burned bituminous coal from Appalachian sources.
The majority of fly ash particles are glassy spheres mainly composed of amorphous or
glassy aluminosilicates, crystalline matter, and carbon. Figure 3-1 presents a
photograph of ash collected from the ash basin at Duke Energy's Cliffside Steam Station
showing a mix of fly ash and bottom ash at 10 µm and 20 µm magnifications. The
glassy spheres can be observed in the photograph. The glassy spheres are generally
immune to dissolution. During the later stages of the combustion process and as the
combustion gases are cooling after exiting the boiler, molecules from the combustion
process condense on the surface of the glassy spheres. These surface condensates consist
of soluble salts (e.g., calcium (Ca+2), sulfate (SO-2), metals (copper (Cu), zinc (Zn), and
other minor elements (e.g., boron (B), selenium (Se), and arsenic (As)) (EPRI 1994).
The major elemental composition of fly ash (approximately 95 percent by weight) is
composed of mineral oxides of silicon, aluminum, iron, calcium. Oxides of magnesium,
potassium, titanium and sulfur comprise approximately 4 percent by weight (EPRI
1995). Trace elemental composition typically is approximately 1 percent by weight and
may include arsenic, antimony, barium, boron, cadmium, chromium, copper,
manganese, mercury, nickel, lead, selenium, silver, thallium, zinc, and other elements.
For comparison, Figure 3-2 shows the elemental composition of fly ash and bottom ash
compared with typical values for shale and volcanic ash. Table 3-1 shows the bulk
composition of fly ash and bottom ash compared with typical values for soil and rock.
In addition to these constituents, fly ash may contain unburned carbon. Bituminous
coal ash typically yields slightly acidic to alkaline solutions (pH 5 to 10) on contact with
water.
The geochemical factors controlling the reactions associated with leaching of ash are
complex. Factors such as the chemical speciation of the constituent, solution pH,
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solution-to-solid ratio, and other factors control the chemical concentration of the
resultant solution. Constituents that are held on the glassy surfaces of fly ash such as
boron, arsenic, and selenium may initially leach more readily than other constituents.
As noted in Table 3-1, aluminum, silicon, calcium, and iron represent the larger
fractions of fly ash by weight. Calcium and iron may limit the release of arsenic by
forming calcium-arsenic precipitates. Formation of iron hydroxide compounds may
also sequester arsenic and retard or prevent release of arsenic to the environment.
Similar processes and reactions may affect other constituents of concern; however,
certain constituents such as boron and sulfate will likely remain highly mobile.
In addition to the variability that might be seen in the mineralogical composition of the
ash, based on different coal types, different age of ash in the basin, etc., it is anticipated
that the chemical environment of the ash basin varies over time, distance, and depth.
EPRI (2010) reports that 64 samples of coal combustion products (including fly ash,
bottom ash, and flue gas desulfurization residue) from 50 different power plants were
subjected to USEPA Method 1311 Toxicity Characteristic Leaching Procedure (TCLP)
leaching and no TCLP result exceeded the TCLP hazardous waste limit. Figure 3-3
provides the results of that testing. The report also presents the trace element
concentrations for fly ash and bottom ash compared to USEPA Residential Soil
Screening Levels (RSLs) for ingestion and dermal exposure. Figure 3-4 shows the 10th to
90th percentile range for trace element concentrations (mg/kg) in fly ash and the
associated USEPA RSLs. The trace element concentrations for arsenic were greater than
the RSL for arsenic. The RSLs of the remaining constituents were greater than or within
the 10th to 90th percentile range for their trace element concentrations.
Figure 3-4 also shows similar data for bottom ash. As with fly ash, the trace element
concentrations for arsenic in bottom ash were greater than the RSL for arsenic. The RSL
for chromium was within the range of concentrations for chromium in bottom ash and
the trace element concentrations for the remaining constituents were below their
respective RSLs.
3.4 Description of Ash Basins and Other Ash Storage Areas
The ash management area consists of three locations; the FADA, the 1971 ash basin and
the 184 ash basin. The FADA appears to have been a low-lying area that was filled with
ash. The thickness of the ash encountered at AB-2 extended from the ground surface to
a depth of approximately 8 feet thick. Groundwater was measured at approximately 3
feet bls at ABMW-2.
The 1971 ash basin area appears to have been excavated below grade to a depth of
approximately 40 feet. Samples collected from AB-1 indicate surficial sand was
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removed, except for approximately two feet at the bottom prior to placement of the ash.
The ash is approximately 79 feet deep, as measured from the top of the ash, at AB-1 and
the top of the ash basin is approximately 40 feet above Site grade. The water level in
ABMW-1 was measured at approximately 34 feet bls. There is a small area of standing
water in the northwest portion of the 1971 ash basin. The excavated sand may have
been used locally in the construction of the basin or canal berms. Both the FADA and
the 1971 ash basins are unlined.
The 1984 basin appears to have been constructed above grade and is lined with a 12-
inch clay layer. The northern portion of this basin contains standing water.
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4.0 RECEPTOR INFORMATION
The Site is located northwest of Wilmington on the west side of Highway 421. The
topography at the Site is relatively gentle, generally sloping downward toward the
Cape Fear River to the west and south. The Site is bounded to the west by the Cape
Fear River, to the north by undeveloped land, to the east by a sand quarry and light
industrial use properties. Residential properties are located southeast of the
southeastern property boundary.
Properties located within a 0.5 mile radius of the Site ash management area compliance
boundary are located in New Hanover County, North Carolina, with the exception of
an undeveloped portion of land on the west side of the Cape Fear River in Brunswick
County. The properties are primarily used for commercial and industrial purposes.
There are no residential properties located within the 0.5 mile radius of the compliance
boundary.
The ash basins are impounded by earthen dikes. The ash basin system was an integral
part of the plant’s wastewater treatment system which received inflows from the ash
removal system, plant yard drain sump, and storm water flows.
Locations of subsurface utilities in the plant area to 1,500 feet beyond the basin
boundary are exhaustive and difficult to complete and map with certainty. Due to the
isolation of the ash basin from the plant area, subsurface utilities are not expected to be
major contaminant flow pathways. Identification of piping near and around the ash
basin was conducted by Stantec in 2014 and utilities around the Site property were also
included on a 2014 topographic map by WSP (Attachment 2) to meet this NCDENR
requirement.
4.1 Summary of Receptor Survey Activities
Surveys to identify potential receptors for groundwater including public and private
water supply wells (including irrigation wells and unused or abandoned wells) and
surface water features within a 0.5-mile radius of the Site compliance boundary have
been reported to NCDENR (SynTerra, Drinking Water Well and Receptor Survey,
September 2014, and Supplement to Drinking Water Well and Receptor Survey, November
2014). These reports are included in Attachment 3. The first report included results of a
review of publicly available data from NCDENR Department of Environmental Health,
NC OneMap GeoSpatial Portal, DWR Source Water Assessment Program online
database, the Cape Fear Public Utility Authority (CFPUA), county geographic
information system, Environmental Data Resources, Inc. records review, the United
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States Geological Survey National Hydrography Dataset, as well as a vehicular survey
along public roads located within 0.5 mile radius of the compliance boundary.
The first report indicated that no wellhead protection areas or surface water bodies are
located within a 0.5 mile radius of the compliance boundary (Appendix B). The Site
cooling pond (Lake Sutton) and the Cape Fear River are located adjacent to the Site to
the west, however, these surface water bodies are not used as drinking water sources.
Approximately 32 possible private water supply wells were observed, were reported, or
were assumed to be located within the survey area, within 0.5 mile of the compliance
boundary. This includes eight on-site wells used for Site operations.
The second report supplemented the initial report with information obtained from
questionnaires sent to owners of property within the 0.5 mile radius of the compliance
boundary. The report included a sufficiently scaled map showing the ash basin
location, the facility property boundary, the waste and compliance boundaries, all
monitor wells, and the approximate location of identified water supply wells. A table
presented available information about identified wells including the owner's name,
address of well location with parcel number, construction and usage data, and the
approximate distance from the compliance boundary.
The questionnaires were designed to collect information regarding whether a water
well or spring is present on the property, its use, and whether the property is serviced
by a municipal water supply. If a well is present, the property owner was asked to
provide information regarding the well location and construction information. The
results from the previous survey and the questionnaires indicated approximately 34
wells might be located within or in close proximity to the survey area (reported wells,
observed wells, and possible wells), including the eight on-site production wells at the
Site.
4.2 Summary of Receptor Survey Findings
Aquifers beneath the Site, including the surficial aquifer, are used for water supply in
the Site vicinity. The Site is likely a recharge area for these aquifers.
Public Water Supply Wells 4.2.1
Four Cape Fear Public Utility Authority public supply wells were identified
adjacent to or near the southeastern boundary of Site:
NHC-SW 1(abandoned) 1,100 feet east of property line
NHC-SW 2(not in use) adjacent, east of property line
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NHC-SW 3 650 feet east of property line
NHC-SW 4 800 feet east of property line
Public water supply wells NHC-SW3 and NHC-SW4 are routinely monitored for
Site COIs.
Private Water Supply Wells 4.2.2
Surveys to identify potential receptors including public and private water supply
wells (including irrigation wells and unused or abandoned wells) and surface
water features within a 0.5-mile radius of the Site compliance boundary have
been reported to NCDENR (SynTerra, Drinking Water Well and Receptor Survey,
September 2014, and Supplement to Drinking Water Well and Receptor Survey,
November 2014). The first report included results of a review of publicly
available data from NCDENR Department of Environmental Health, NC
OneMap GeoSpatial Portal, DWR Source Water Assessment Program online
database, county geographic information system, Environmental Data Resources,
Inc. records review, the United States Geological Survey National Hydrography
Dataset, as well as a vehicular survey along public roads located within 0.5 mile
radius of the compliance boundary.
During 2015, NCDENR managed the sampling of water supply wells within or
near the survey area. The data are provided in Appendix B.
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5.0 REGIONAL GEOLOGY AND HYDROGEOLOGY
According to the Geologic Map of North Carolina, published by the North Carolina
Department of Natural Resources and Community Development (1985), the Site lies
within the Coastal Plain Physiographic Province. The following section provides a
regional understanding of the hydrogeology of the Coastal Plain area and may not
represent actual conditions at the Site.
The North Carolina Coastal Plain is approximately 90 to 150 miles wide from the
Atlantic Ocean westward to its boundary with the Piedmont province. Two natural
subdivisions of the Coastal Plain were described by Stuckey (1965): the Tidewater
region and the Inner Coastal Plain. The Site is located within the Tidewater region,
which consists of the coastal area where large streams and many of their tributaries are
affected by ocean tides (Winner, Jr. and Coble, 1989). The Site is located on the east side
of the Cape Fear River within the alluvial plain between the coastal dunes and the
interior uplands (NUS Corporation, 1989).
5.1 Regional Geology
The Coastal Plain comprises a wedge shaped sequence of stratified marine and non-
marine sedimentary rocks deposited on crystalline basement. The sedimentary
sequences range in age from recent to lower Cretaceous (Narkunas, 1980).
The surficial sands are underlain by the Pee Dee Formation in the Site area. In the
Wilmington area, the Pee Dee confining unit has an average thickness of 10 feet. The
Pee Dee Formation contains fine to medium grained sand interbedded with gray to
black marine clay and silt. Sand beds are commonly gray or greenish gray and contain
varying amounts of glauconite. Thin beds of consolidated calcareous sandstone and
impure limestone are interlayered with the sands in some places. The Pee Dee
Formation contains a confining unit at the top in areas south of the Site; however the
Pee Dee confining unit below the surficial sands was not encountered at the Site.
5.2 Regional Hydrogeology
In the eastern part of the North Carolina Coastal Plain, groundwater is obtained from
the surficial, Castle Hayne, and Pee Dee Formations. The Coastal Plain groundwater
system consists of aquifers comprised of permeable sands, gravels, and limestone
separated by confining units of less permeable material.
According to Winner, Jr. and Coble (1989), the surficial aquifer consists primarily of fine
sands, clays, shells, peat beds, and scattered deposits of coarse-grained material in the
form of relic beach ridges and floodplain alluvium. The areal extent of the surficial
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aquifer in the Coastal Plain is approximately 25,000 square miles with an average
thickness of 35 feet. The average estimated hydraulic conductivity is 29 feet per day
(Winner, Jr. and Coble, 1989).
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6.0 SITE GEOLOGY AND HYDROGEOLOGY
Two sedimentary geologic units (Coastal Plain surficial deposits and the Pee Dee
Formation) have been encountered in exploratory borings installed at the Site (Figure 1-
2). The surficial deposits extend to approximately 50 feet below ground surface (bgs)
and consist of medium-fine to coarse grained sands with laterally inconsistent beds of
coarse sand and fine gravel in the lower 30 feet. The Pee Dee Formation lies
unconformably below the surficial sands and consists of fine sands and silts with
occasional clay lenses.
The Site investigation conducted in accordance with the GAP (Section 3.2) included
installation of soil borings, groundwater monitor wells, borings in and through the 1971
ash basin and FADA, and installation of an additional well to sample ash pore water
(Table 6-1 [revision of Table 9 from the GAP]). Physical and chemical properties of soil
samples collected from the borings and wells and sediment samples collected from
ditches and streams were determined (Table 6-2). Chemical analyses of a broad list of
potential constituents of concern were conducted on samples of groundwater and
surface water from the cooling pond and the Cape Fear River (Table 6-3).
Ten monitoring well pairs were installed on-site north, east and southeast of the ash
basins; six monitoring well pairs were installed on off-site properties east of the Site and
two monitoring well pairs (ABMW-1S/D and ABMW -2S/D) were installed within the
1971 ash basin and the FADA. These wells were installed in accordance with GAP
Sections 7.1.2 and 7.1.3 (Table 6-1, Table 6-4, Appendices C and E). Based on
preliminary data, seven additional deep wells were added off-site (SMW-6D) and on-
site at AW-2D, AW-5D/E, AW-6E and MW-23E.
Ten soil borings, designated confining unit borings (CUBs), were performed in the
southeastern and southern portions of the Site. The borings extended through the
surficial deposits to the underlying Pee Dee Formation in an attempt to locate the Pee
Dee confining unit. The confining unit is not present at the Site within the area of this
assessment.
The primary technical objectives for the new well locations was to establish perimeter
boundary conditions for the groundwater modeling that will be used to develop the
CAP for the Site and to develop additional background data on groundwater quality.
These well installations were selected to anchor strategically positioned flow path
transects to facilitate model analysis (Figure 1-2). Flow from the 1971 ash basin to
potential receptor areas is to the east and southeast. No potential receptors were
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identified to the west. Three transects were selected for the Site to illustrate flow path
conditions in the vicinity of the ash basins. Section A-A’ provides the best illustration of
the ash basins source area and FADA (basin dams, canals and ash) in relation to the
upland area to the north and receptor area to the southeast. Sections B-B’ and C-C’
illustrate conditions from the Cape Fear River eastward through the Site property.
Specific objectives for each location follow:
To refine the horizontal and vertical extent of metals in the aquifer, five
additional well pairs (AW-1B/C through AW-5B/C) were installed along the
property line east of the ash management area. The wells were installed as well
pairs to also provide vertical information on aquifer chemistry and vertical
gradients. Additional deep wells AW-2D, AW-5D/E and AW-6E were added to
provide further vertical delineation at those locations.
Well pair AW-6B/D and monitor well AW-7D were installed adjacent to
previously existing wells MW-12 and MW-31C, downgradient from the ash
management area. These wells were installed to provide information on the
vertical distribution of constituents of concern at these locations. A proposed
monitor well, AW-7B, was originally proposed but not installed when it was
determined that MW-31B was appropriately constructed to monitor the
targeted flow zone.
To further define water quality beyond the compliance boundary to the north,
monitor wells AW-8B/C were installed north of well MW-27B. MW-9B/C were
installed south of the MW-7 well cluster to address groundwater conditions
beyond the compliance boundary southeast of the 1971 ash basin and FADA.
Monitor well pair MW-37B/C were installed to address background
groundwater conditions further south of MW-4B.
In addition to assessment well clusters AW-1 through AW-9, sentinel well
clusters (SMW-1B/C through SMW-6B/C/D) were installed to monitor
groundwater conditions between nearby receptors and the property boundary
for the Site.
The GAP designated monitor wells according to depth, with “A” meaning a shallow
well in the upper 15 feet, and subsequently deeper wells designated, “B”(25 feet), “C”
(45 feet) or “D” (100 feet). The “E” (150 feet) designation was added when deeper wells
were required based on preliminary assessment data.
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Based on historical Site data, COIs typically have not been detected at concentrations
greater than 2L or IMAC in the shallow (water table) portion of the aquifer. Therefore,
no shallow wells (“A” designation) were installed. Shallow intermediate wells (“B”
designation) were installed at a depth of approximately 20 to 25 feet within the middle
section of the surficial aquifer. Deep intermediate monitor wells (“C” designation) were
installed in the lower surficial aquifer at a depth of 40 to 45 feet bgs.
The GAP proposed deep wells to be installed on top of a confining unit at the base of
the surficial aquifer, at an estimated depth 75 feet bgs. However, a confining unit was
not encountered and the top of the Pee Dee was established to be at approximately 50
feet bgs. Therefore deep wells designated as “D” wells were installed within the Pee
Dee formation at a depth of approximately 100 feet bgs. Additional, deeper, wells
designated as “E” wells, were installed to a depth of 150 feet bgs at AW-5, AW-6 and
MW-23 (Figure 1-2).
Each of the wells were installed as a single cased monitoring well, with the exception of
ABMW-2D in the FADA, which is cased through the ash to depth of 14 feet bgs. The
well casings consist of two-inch diameter PVC schedule 40 flush-joint threaded casing
and pre-packed screens. The well screen intervals are 5 or 10 feet long for each of the
monitor wells.
The annular space between the borehole wall and the pre-packed well screens for each
of the wells was filled with clean, well-rounded, washed, high grade 20/40 mesh silica
sand. The sand pack was placed to at least 2 feet above the top of the pre-packed
screen, and then at least two feet of pelletized bentonite was placed as a seal above the
filter pack. The remainder of the annular space was filled with a neat cement grout
from the top of the upper bentonite seal to near ground surface.
Monitor wells were completed with either steel above ground protective casings or steel
flush-mounted casings with locking caps and well tags. The protective covers were
secured and completed in a concrete collar and 2-foot square concrete pad.
The hydraulic conductivity of each well was tested by the instantaneous change in head
or “slug” test method in accordance with GAP Section 7.1.4 (Appendix C).
Drinking water purchased from New Hanover County was used for drilling fluid. A
sample of the “source water” was analyzed for the full set of GAP parameters
(Attachment 5). No exceedances of 2L were detected in the purchased drinking water
with the exception of iron. GAP COIs antimony, arsenic, boron, barium, cobalt,
manganese, and vanadium were undetected in the sample. Iron was detected at 963
micrograms per liter (µg/L).
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6.1 Site Geology
No consolidated rock outcrops are present at the Site. Areas in the Site and associated
impoundments have been constructed by mass grading resulting in disturbed or
possibly imported geologic materials. Undisturbed areas consist of small sand hills,
low-growth vegetation and pine woods or electric transmission line corridors.
The Site subsurface consists of sands of the surficial aquifer which extend to
approximately 50 feet bgs. The upper 20 feet or so of this unit consists of well-sorted,
light-colored sand, loose to moderately dense with little shell or organics. The lower 30
feet consists primarily of poorly-sorted sands with discontinuous layers of coarse sand
and fine gravel. Thin laminae of silts and clays also occur randomly in the lower
portion of this unit. Wood remnants were also encountered in places near the contact
with the lower Pee Dee Formation.
The surficial sands lie unconformably over the Pee Dee Formation. The contact
between the surficial and the Pee Dee Formation is sharp and distinct due to the dark
grey-green color of the fine sands and silts of the Pee Dee. Trace amounts of large shell
and sandstone were also occasionally observed at this contact.
The Pee Dee Formation extends to the deepest horizon explored (150 feet bgs) during
the assessment. The upper portion of the Pee Dee consists of dark gray or medium to
dark green fine sands and silt with clay lenses and laminae. Below 75 feet, thin layers of
sandstone were encountered; however these were not continuous across the Site. The
Pee Dee becomes finer with depth and often is a very dense, low-plasticity clayey silt.
Geologic cross-sections A-A’, B-B’, and C-C’ are presented in Figures 6-1 and 6-2.
Photographs of sonic drill core from monitor wells and several of the soil borings are
displayed on the geologic cross-sections to illustrate Site geology (Figures 6-3, 6-4, and
6-5). The full set of photographs is included as Attachment 6.
Soil Classification 6.1.1
The surficial aquifer consists of well sorted to poorly sorted (SW/SP) sands which
vary from fine to coarse grained with some fine gravel. The upper zone is
primarily a well-sorted, medium-fine grained sand while the lower portion tends
to be poorly sorted, with larger grain sizes and occasional layers of coarse
sand/fine gravel. Oxide staining (reddish-yellow and orange), were common
near the base of the lower surficial unit. The upper zone typically contains more
fines and fine-grained sand than the lower zone based on samples from AW-8C
and AW-9C.
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The contrast in grain size across the surficial/Pee Dee contact is illustrated by
comparing the grain size analyses of two samples from SMW-2C collected above
and below the contact. Above the contact the sample consists of approximately
78% medium to coarse grained sand. The soil below the contact contained over
70% fine sand, silt or clay-sized particles. Pee Dee sediments at the Site are light
to dark green and dark gray silty fine sands and clayey silts with occasional clay
lenses and thin sandstone layers. The sediments in the upper Pee Dee contain
fewer fines; as exemplified by the grain size analyses on samples collected from
AW-7D at a depth of 99 feet and from AW-5E and MW-23E at a depth of greater
than 140 feet contained over 40% silts or clays whereas samples from the upper
Pee Dee at AW-7D at a depth of 49 feet contained less than 8% fines. Turbidity in
samples collected from these lower zones are higher due to the fines content.
Grain size analyses, moisture content and other physical soil test results are
presented in Appendix F.
Rock Lithology 6.1.2
There are no rocks within the CSA area.
Structural Geology 6.1.3
Due to the unconsolidated nature of the subsurface, structural geology does not
appear to be a factor in the SCM for the Site.
Soil and Rock Mineralogy and Chemistry 6.1.4
Mineralogy and chemistry of the soils encountered are presented in Section 8.
6.2 Site Hydrogeology
The surficial unconfined aquifer is the first major hydrostratigraphic unit at the Site. As
discussed in Section 6.1, the upper portion of the surficial aquifer is more uniform in
structure and grain size, primarily consisting of well sorted sands. The lower portion
varies greatly in grain size, with poorly-sorted sands interbedded with numerous
coarse-grained layers containing fine gravel and occasionally with thin silt laminae.
The upper portion grades into the lower portion between 15 and 25 feet bgs.
The Pee Dee Formation directly underlies the surficial zone at the Site. In areas south of
the Site a confining unit is reported to be present between the surficial zone and the Pee
Dee Formation; this confining unit was not found to be present at the Site. As described
in Section 6.1, the contact between the Pee Dee Formation and the overlying surficial
unit is sharp and with greatly contrasting soil types. It is anticipated that the less
permeable sediments of the Pee Dee would impede vertical groundwater flow and flow
within the coarse-grained layers would be significantly higher. This is discussed
further in Section 6.2.3
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The first occurrence of groundwater at the Site is in the surficial aquifer at depths
ranging from 3 to 17 feet bls. Groundwater elevations in June 2015 (Table 6-5) indicate
the groundwater flow direction in the upper and lower portions of the surficial aquifer
beneath the ash basins flows radially from the central sand hills portion of the Site,
indicating this is likely a local recharge area. Generally, groundwater flows east,
southeast and south from the Site. Water level data from the Pee Dee formation
indicates groundwater flow to the east and south. The presence of high capacity
industrial and public water supply pumping wells near the Site complicates the
determination of groundwater flow. This will be clarified upon completion of the
groundwater flow model.
Groundwater Flow Direction 6.2.1
Potentiometric surface maps for the upper surficial, lower surficial, and Pee Dee
aquifers are presented as Figures 6-6, 6-7, and 6-8, respectively. The initial zone
of saturation is comprised of pore water within the ash basins and shallow
sediment. Groundwater gradients in the surficial aquifer are affected by
manmade features (plant area, cooling pond), the ash basin, Site production
wells and off-site public supply wells, production wells for the Invista plant, and
production wells for the ST Wooten facility and Site geology. If the proposed
extraction wells are installed along the eastern property line these will also affect
groundwater flow direction in the surficial and Pee Dee formations.
Additionally, when the CFPUA wells adjacent to the Site to the east, are
removed, alteration of groundwater flow is anticipated in that area.
The water table at the Site is typically located at depths of approximately 3 to 18
feet bgs, depending on antecedent precipitation and topography. The surficial
aquifer groundwater flow regime of the Site is hydraulically bounded on the
west by the cooling pond and the Cape Fear River which flows south. The
Northeast Cape Fear River is approximately one mile east of the Site and regional
groundwater flow is anticipated to be south in the areas between the two rivers.
The Site is located on a peninsula defined by the Cape Fear River, adjacent to the
west and the Northeast Cape Fear River, located approximately one mile to the
east. Based on regional topography and drainage features, groundwater flow
within this peninsula would be either to the west or east to one of the two rivers
or to the south where the rivers converge. At the Site, groundwater flows
radially from the 1971 and 1984 ash basins. Along the eastern edge of the cooling
pond, groundwater flows to the west. On the east side of the 1971 basin,
groundwater flows to the east, southeast and south. In the area of the FADA,
groundwater flows to the southwest. A groundwater divide or ridge is located
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northeast of the ash basin which roughly corresponds to the presence of small
sand hills in that area. A zone of slightly depressed water levels is centered
around the Site production wells and the CFPUA wells in the southeast portion
of the Site.
The potential influence from the off-site municipal and industrial production
wells (and the potential extraction wells) will be factored into the groundwater
flow model being prepared for the CAP. As the model is being prepared
additional groundwater and surface water elevation monitoring data may be
collected.
Hydraulic Gradients 6.2.2
Horizontal hydraulic gradients were calculated using data collected from surface
water and monitoring well locations on June 1st, 2015 (Table 6-6 and Figure 6-6,
6-7, and 6-8). The gradients ranged from 0.00009 foot per foot (ft./ft.) to 0.001
ft./ft.
Hydraulic Conductivity 6.2.3
Slug tests were conducted at each newly-installed CSA groundwater monitoring
wells and were analyzed for hydraulic conductivity in accordance with GAP
Section 7.1.4 (Table 6-7, Appendix G). Infiltration tests using Guelph
permeameters were deemed unnecessary by the groundwater model developer
since the slug test data is available.
Hydraulic conductivity of upper surficial aquifer wells range from 1.64 x 10-5 to
7.00 x 10-2 cm/sec. Wells screened in the lower surficial aquifer range from 1.74 x
10-3 cm/sec to 6.14 x 10-2 cm/sec. Wells screened in the upper Pee Dee Formation
have a geometric mean value of 1.3 x 10-5 cm/sec and wells in the lower Pee Dee
have a mean value of 2.72 x 10-7 cm/sec. Vertical hydraulic conductivity results
for undisturbed samples from the upper Pee Dee fine sands and clayey silts are
relatively low (6.7 x 10-4 cm/sec to 1.5 x 10-7 cm/sec, Table 6-8). The higher
conductivity values in the Pee Dee were recorded for samples near the contact
with the surficial, which has fewer fines than the soils deeper in the formation.
These data indicate that lateral groundwater flow will predominate over
downward vertical flow at the Site. Accordingly, lateral migration of COIs
would be expected relative to vertical migration.
Groundwater Velocity 6.2.4
Groundwater velocities calculated for the four flow paths described in Section
6.2.2. range from 0.185 to 8.55 feet per year. Slug tests that were conducted in
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wells screened below the ash basin were analyzed for hydraulic conductivity and
were used to calculate the flow velocity. Flow rates from the ash basins to
surrounding areas are the highest due to the hydraulic gradient from the basins
to the surrounding areas.
Effects of Geologic/Hydrogeologic Characteristics on 6.2.5
Contaminants
The retardation factor of subsurface soils will be determined by Kd analyses, the
results of which are pending. These results will be incorporated in the
preparation of the CAP.
6.3 Hydrogeologic Site Conceptual Model
The hydrogeologic site conceptual model (SCM) is based on the configuration of the ash
basins relative to Site features including canals, ponds, rivers and production wells
(Figure 6-9). The contrasting permeability between the surficial and Pee Dee formation
is a significant part of in this model.
The 1971 ash basin was excavated below the water table to a depth of approximately 40
feet below grade. All but the lower two feet of the surficial sands were removed by this
excavation; therefore the ash in the 1971 basin sits just above the contact between the
surficial and Pee Dee formations. The ash is approximately 80 feet with over half of that
saturated. Infiltration of surface water causes some mounding in this basin, resulting in
radial groundwater flow away from the mounded area. The discharge canal to the
south and the cooling pond to the west control groundwater elevation in the surficial
aquifer to the west and south of the 1971 ash basin.
Small sand hills located in the northeast portion of the Site create a localized
groundwater divide extending roughly north and south. Surficial groundwater also
flows radially from this area.
The surficial aquifer has larger hydraulic conductivity values than does the underlying
Pee Dee Formation, resulting in preferential lateral flow. This lateral flow, especially in
the lower surficial aquifer, is affected by the presence of surface water bodies and by the
operation of production wells located along the eastern Site property boundary. There
is a downward vertical gradient between the upper and lower surficial aquifer wells in
most locations and a downward vertical gradient between the surficial and Pee Dee
formations. Although because of the lower hydraulic conductivities, the flux of water is
greater in the shallow formations (above the Pee Dee).
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6.4 Geochemical Site Conceptual Model
This section contains geochemical information on the COIs for the Site groundwater
assessment. This information provides a necessary context for the data collected to
characterize the ash basin source area and potential receptors. Data from published
sources address the relative abundance of each COI in the rocks at the earth surface
(“crust”), the occurrence of the elements in coal, the leaching characteristics of ash, and
fate and transport of COIs that might be released to the environment. Based on
exceedances of 2L or IMAC in samples of ash pore water and groundwater, iron,
vanadium, manganese, boron, barium, arsenic, cobalt and antimony (listed in order of
prevalence) are addressed in the following paragraphs.
Iron 6.4.1
Iron has been detected in samples above the 2L in most monitor wells across the
property, including background wells. Iron is estimated to be the fourth most
abundant element in the Earth’s crust at approximately five weight percent
(Parker, 1967, Table 18 and Figure 3). Oxygen (46.60 weight percent), silicon
(27.72 weight percent), and aluminum (8.13 weight percent) occur in higher
concentrations. Iron occurs in divalent (ferrous, Fe+2), trivalent (ferric, Fe+3),
hexavalent (Fe+6), and Fe-2 oxidation states. Iron is a common mineral forming
element, occurring primarily in mafic (dark colored) minerals including micas,
pyrite (iron disulfide), and hematite (iron oxide), as well as in reddish colored
clay minerals.
Clay minerals and pyrite are common impurities in coal. Under combustion
conditions in a coal-fired boiler, clay minerals would be dehydrated to mullite or
gibbsite, possibly liberating iron, and pyrite would oxidize to hematite or
magnesioferrite. Research summarized by Izquierdo and Querol (2012) indicates
that iron leaching from coal ash is on the order of one percent of the total iron
present due to the low pH required to solubilize iron minerals. Despite the low
apparent mobilization percentage, iron can be one of the COIs detected in the
highest concentrations in ash pore water.
Ferric iron is soluble at pH less than 2 at typical surface conditions (25°C and 1
atmosphere total pressure, Schmitt, 1962). For this reason, dissolved iron in
surficial waters is typically oxidized to the trivalent state resulting in formation
of ferric iron oxide flocculation that exhibits a characteristic reddish tint.
Vanadium 6.4.2
Analysis for vanadium in groundwater samples from the Site was initiated with
the 2015 groundwater assessment. Exceedances of the former IMAC of 0.0003
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mg/L were detected in samples from each of the ash pore well locations; and in
many samples from each of the depth horizons sampled. Vanadium is estimated
to be the 22nd most abundant element in the crust (0.011 weight percent, Parker,
1967). Vanadium occurs in four oxidation states (V+5, V+4, V+3, and V+2). It is a
common trace element in both clay minerals and plant material.
The National Uranium Resource Evaluation (NURE) program was initiated by
the Atomic Energy Commission in 1973 with a primary goal of identifying
uranium resources in the United States (http://pubs.usgs.gov/of/1997/ofr-97-
0492/, accessed on June 8, 2015). The Hydrogeochemical and Stream Sediment
Reconnaissance program (initiated in 1975) was one component of NURE.
Planned systematic sampling of the entire United States began in 1976 under the
responsibility of four Department of Energy national laboratories. Samples were
collected from 5,178 wells across North Carolina. Of these, the concentration of
vanadium was equal to or higher that the former IMAC of 0.0003 mg/L in 1,388
well samples (27 percent).
Manganese 6.4.3
Manganese was detected above 2L in more samples at the Site than any other
metal except iron. The majority of the 2L exceedances occur in the surficial
aquifer; with 2L exceedances in the Pee Dee limited to wells below or adjacent to
the ash basins with the exception of AW-2D and PZ-10 in the northern portion of
the Site. Manganese is estimated to be the 12th most abundant element in the
crust (0.100 weight percent, Parker, 1967). Manganese exhibits geochemical
properties similar to iron with Mn+7, Mn+6, Mn+4, Mn+3, Mn+2, and Mn-1 oxidation
states. Manganese substitutes for iron in many minerals. Similar to iron,
manganese leaching from coal ash is limited to less than 10 percent of the total
manganese present due to the low pH required to solubilize manganese minerals
(Izquierdo and Querol, 2012). Despite the low apparent mobilization percentage,
manganese can be detected in relatively high concentrations in ash pore water.
Boron 6.4.4
High concentrations of boron (over 5 times 2L) were detected in the ash pore
water sample from the 1971 ash basin and were also detected in several wells
screened in the lower surficial aquifer and the Pee Dee.
Boron is a trace element in the crust, with estimated concentrations ranging from
as little as 1 mg/kg in mafic igneous rocks to hundreds of milligrams per
kilogram in clay rich rocks (Parker, 1967, Table 19). It occurs only in the trivalent
form (B+3). Boron is concentrated in sedimentary rocks like those that underlie
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the Site (Urey, 1953). This observation indicates that a mechanism exists to
concentrate boron in minerals since the oceans could dissolve all of the boron
estimated to be present in the crust (Fleet, 1965). Fleet presents both biogenic
and mineralogical processes to account for the preferential concentration of
boron in the crust. Boron is a micronutrient (Goldberg, 1997) that is concentrated
in plant tissue, including the plants from which coal formed.
Because boron is associated with the carbon (fuel) in coal, it tends to volatilize
during combustion and subsequently condense onto fly ash as a soluble borate
salt (Dudas, 1981). Boron leaches readily (up to 50 percent of total present) and
rapidly from fly ash (Cox et al., 1978). Boron is considered a marker COI for coal
because boron impact is rarely associated with other types of industrial activities.
Boron is the primary component of very few minerals. Tourmaline, a rare gem
mineral, forms under high temperature and pressure (Hurlbut, 1971). The
remaining common boron minerals, including borax that was mined for laundry
detergent in Death Valley, form from the evaporation of seawater in deposits
known as evaporites. For this reason, boron mobilized into the environment will
remain in solution until incorporation into plant tissue or adsorption by a
mineral. Boron is commonly occurs in salt water and has been detected in wells
within the Pee Dee Formation in the region of the Site. A well located in Myrtle
Beach South Carolina and screened from 95 - 105 feet within the Pee Dee
formation was reported to contain a concentration of 1,600 µg/L of boron.
(Ground-Water Quality Data From the Southeastern Coastal Plain, Mississippi,
Alabama, Georgia, South Carolina, and North Carolina, Roger W. Lee, U. S. Geological
Survey, Open File Report 84-237, 1984).
Fleet describes sorption of boron by clays as a two-step process. Boron in
solution is likely to be in the form of the borate ion (B(OH)4 −. The initial
sorption occurs onto a charged surface. Observations that boron does not tend to
desorb from clays indicates that it migrates rapidly into the crystal structure,
most likely in substitution for aluminum. Goldberg et al. (1996) determined that
boron sorption sites on clays appear to be specific to boron. For this reason, there
is no need to correct for competition for sorption sites by other anions in
transport models.
Goldberg (1997) lists aluminum and iron oxides, magnesium hydroxide, clay
minerals, calcium carbonate (limestone), and organic matter as important
sorption surfaces in soils. Boron sorption on oxides is diminished by competition
from numerous anions. Boron solubility in groundwater is controlled by
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adsorption reactions rather than by mineral solubility. Goldberg concludes that
chemical models can effectively replicate boron adsorption data over changing
conditions of boron concentration, pH, and ionic strength (p. 43).
Arsenic 6.4.5
Arsenic was detected in the ash pore water well samples and a few wells in the
lower surficial and Pee Dee Formation below or near the ash basins. Arsenic is a
trace element in the crust, with estimated concentrations ranging from less than 1
mg/kg in mafic igneous rocks to 13 mg/kg in clay rich rocks (Parker, 1967, Table
19). It occurs in multiple valence states (As+5, As+3, and As-3). Arsenic in coal
occurs primarily in pyrite (iron sulfide, with arsenic replacing iron in the crystal
structure) (Finkelman, 1995). Arsenic condenses on fly ash as arsenate (As+5)
(Goodarzi et al., 2008). Leaching tests on ash indicate that trace quantities up to
50 percent of the arsenic present can be leached. In addition to the solubility of
the source, the concentration of calcium and presence of oxides appear to limit
the mobility of arsenic (Izquierdo and Querol, 2012).
Cobalt 6.4.6
Cobalt was detected above IMAC in several upper surficial aquifer wells and
most lower surficial aquifer wells but not in any of the Pee Dee Formation wells.
Cobalt is a base metal that exhibit geochemical properties similar to iron and
manganese. Each occurs as a divalent and trivalent ion. Cobalt can occur as Co-1.
In terms of distribution in the crust, cobalt exhibits a strong affinity for mafic
igneous and volcanic rocks and deep-sea clays (Parker, 1967, Table 19).
Cobalt occurs in clay minerals and substitutes into the pyrite crystal structure.
There is also evidence that it is organically bound in coal (Finkelman, 1995).
Izquierdo and Querol (2012) report limited leaching of cobalt from coal,
attributing this observation to incorporation into iron oxide minerals.
6.5 Electrochemical Charge Balance
Constituents dissolved in solution exhibit either positive (called cations, such as Fe+2) or
negative (anions, such as HCO3-) charges because they are not chemically bound in a
solid. Comparison of the concentration of major cations and anions in a solution such
as a groundwater sample can be used for two purposes. First, charge balance within a
small tolerance (five to ten percent) provides an indication that all of the major
constituents have been identified. Second, lack of charge balance in a well characterized
sample can be an indication of disequilibrium.
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Electrochemical charge balance is calculated by converting concentrations of major
cations (calcium, potassium, sodium, magnesium, iron, and manganese) and major
anions (chloride, bicarbonate + carbonate, sulfate + sulfide, and nitrate + nitrite) to molar
equivalents, summing the total of each, and comparing the results as a percentage off
equality. Groundwater that is in equilibrium with the soil or rock that surrounds it
should exhibit equal concentrations of cations and anions (refer to Section 6.4.5). Lack
of charge balance can be an indication that other chemical constituents are “major”
cations or anions.
Lack of charge balance can also be an indication of disequilibrium. The chemical
weathering that occurs as rainwater infiltrates into the ground everywhere in the
southeastern United States is the result of chemical disequilibrium. If the rainwater
were in equilibrium with soil and rock, weathering would not occur. Similarly,
discharge of contaminants from a source can cause disequilibrium in affected
groundwater as reactions initiated by the introduced contaminants proceed.
Groundwater samples collected for the CSA were analyzed for a large suite of cations
and anions. It is unlikely that anions, in particular, have not been fully characterized.
Deviations in solution chemistry indicated by charge balance calculations are evaluated
in this report to identify a cause.
6.6 Equilibrium
The conditions under which chemical reactions such as the binding of dissolved arsenic
into an iron oxide can be determined by experiments conducted under highly
controlled, or equilibrium, conditions (Nash, 1971, p. 101-107). These experimental data
yield powerful predictive capabilities regarding the results of chemical reactions so long
as the assumption of equilibrium can be made.
Equilibrium is attained over time when the entropy (S, defined as the chemical capacity
for change) of the reaction reaches a maximum for the conditions (e.g., temperature,
pressure, concentration, etc.) under which the reaction is occurring. Equilibrium
calculations do not address the time required for entropy to reach a maximum
(Denbigh, 1971, p.40-42). In general, conditions at the surface of the earth are not
conducive to driving reactions to the maximum level of entropy, or equilibrium. It is
for this reason that chemists use reactors to create conditions of elevated temperature
and pressure to convert a mixture of chemicals into a product in a short period of time.
For these reasons, use of equilibrium equations to predict the results of chemical
reactions in an ash basin or in the shallow subsurface of the earth is at best an
approximation. These equations are a proper and appropriate starting point to predict
the chemical reactions that will occur over time as ash sluice water accumulates in a
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basin, becomes ash pore water, and subsequently migrates from the basin. However,
because the assumption that equilibrium will be attained cannot be supported, the
predictions in this report and subsequent documents based on such calculations are
approximations and must be critically evaluated with professional judgment.
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7.0 SOURCE CHARACTERIZATION
The groundwater assessment was focused on the ash basins and FADA at the Site as
potential sources of groundwater impact, as described in the following sections.
Methods used to characterize the source materials are described in Appendix C.
7.1 Identification and Description of Sources
Coal is formed from plant material that accumulated in settings comparable to modern
day swamps. Coalification is the process by which plant material is converted to coal by
elevated heat and pressure that result from burial beneath overlying soil and rock.
Varying amounts of inorganic sediment such as sand, silt, and clay are deposited in
swamps with the dead plant material. Additional inorganic impurities such as pyrite
likely formed from interstitial liquids as the plant material was converted to coal. The
chemical character of coals evolves in a regular manner with increasing depths of burial
and passage of time. Depth ranges up to 2,000 meters (6,560 feet) BGS and temperature
ranges of 70° to 80°C (158° to 176°C) are accepted as the conditions under which coals
form (Kisch, 1969, p. 407-425; Turner, 1981, p. 303-305).
Coal Combustion and Ash Handling System 7.1.1
Coal was pulverized prior to combustion in the boilers. Bottom ash is comprised
primarily of the inorganic impurities in coal that did not burn in the boiler. The
grain size or specific gravity of this material prevents entrainment in the flue gas.
Fly ash is fine material that was removed from the flue gas stream by
electrostatic precipitators at the Site. Electrostatic precipitators went into service
at the Site between 1972 and 1975 for the three coal-fired units. Ash was
conveyed hydraulically from the plant boilers to the FADA area first and then to
the ash basins. During operation, ash laden sluice water flowed by gravity to a
pump pit for conveyance by pipe to the ash basin. Hydraulic placement of ash
was accomplished by moving the influent pipe to different locations within the
basins. Ash particles settled in the basin while the water was impounded.
Description of Ash Basins 7.1.2
The FADA appears to have been a low-lying area that was filled with ash. The
thickness of the ash encountered at AB-2 extended from the ground surface to a
depth of approximately 8 feet thick. Groundwater was measured at
approximately 3 feet bgs at ABMW-2.
The 1971 ash basin area appears to have been excavated below grade to a depth
of approximately 40 feet. Samples collected from AB-1 indicate surficial sand
was removed, except for approximately two feet at the bottom prior to placement
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of the ash. The ash is approximately 79 feet deep, as measured from the top of
the ash, at AB-1 and the top of the ash basin is approximately 40 feet above Site
grade. The water level in ABMW-1 was measured at approximately 34 feet bgs.
There was a small area of standing water in the northwest portion of the 1971 ash
basin during this assessment (2015). The excavated sand may have been used
locally in the construction of the basin or canal berms. Both the FADA and the
1971 ash basins are unlined.
The 1984 basin appears to have been constructed above grade and is lined with a
12-inch clay layer. The northern portion of this basin contains standing water as
of this assessment (2015).
The ash basin embankments are well vegetated. Soil has been used to construct
the perimeter levees.
According to Duke Energy (October 31, 2014) the 1971 and 1984 ash basins
contain approximately 6,320,000 tons of ash and the FADA area contains
approximately 840,000 tons of ash. No other ash storage facilities have been
identified on the Site property.
7.2 Characterization of Sources
Prior characterization of the ash basin was supplemented by two borings and
installation of two monitor wells during the current assessment. The borings were
installed using sonic drilling methods with continuous sample recovery (Appendix C).
Each boring penetrated the bottom of the ash. Two ash samples from AB-1 and one
from AB-2 and two soil samples were collected from each boring for physical and
chemical testing in accordance with GAP Section 7.1.1. Only one ash sample was
collected from AB-2 due to the thin section of ash at this location.
The contact between ash and underlying soils was distinct in both borings. Physical
intrusion of ash into the underlying soils appears limited.
Physical Properties of Ash 7.2.1
Physical properties (grain size, specific gravity, and moisture content) and
mineralogy determinations were performed on samples from the ash basin.
Physical properties were measured using ASTM methods and mineralogy was
determined by X-ray diffraction (Appendix C). With the exception of the sample
from AB-2, the ash is fine grained (primarily silt with some clay size particles)
and exhibits a lower specific gravity than soils which typically range from 2.2 to
2.5 (Table 7-1).
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Mineralogy was determined for ash samples from AB-1 at 3’-5’ bgs & 43’-45’ bgs
(Table 7-2). The samples tested were predominately quartz (43.1 & 42.3 percent).
The AB-1, 3’-5’ sample contained 23.3 percent calcium, while the AB-1, 43’ -45’
sample contained 34.6 percent aluminum. The AB-2 ash sample from the FADA
was found to contain 70.3 percent quartz.
The ash samples also contained hematite (Fe2O3) which is presumed to have
formed in the boiler from minerals that contained reduced iron (such as pyrite).
Chemical Properties of Ash 7.2.2
Three samples of ash, two from the 1971 basin and one from the FADA were
analyzed for total metals and total organic carbon (TOC). In addition one ash
sample from each the 1971 ash basin and the FADA and submitted for metals
susceptible to leaching by the USEPA Synthetic Precipitation Leaching Procedure
(SPLP, Appendix C).
The 1971 ash basin ash samples were found to contain iron, mercury, and
selenium above the USEPA Mid-Atlantic Risk Assessment Regional Screening
Levels – Protective of Groundwater (Table 7-3). Manganese was detected in
both samples at concentrations well below screening levels, 24.2 mg/kg and 35.2
mg/kg. Boron was detected at estimated concentrations of 8.7 mg/kg and 7.2
mg/kg. Residual carbon (measured as TOC) in the samples ranged from 7,130 to
145,000 mg/kg.
The FADA ash sample contained barium, beryllium, copper, iron, lead, mercury
and selenium above the groundwater screening level as well as aluminum, cobalt
and vanadium in excess of the residential health screening level. Boron was
detected at an estimated concentration of 21.9 mg/kg. Residual carbon
(measured as TOC) was detected at 91,000 mg/kg.
All of the 25 metals analyzed for except beryllium, cadmium, chloride, nitrate,
cobalt, iron, lead, thallium and vanadium in the 1971 ash basin sample and
cadmium, chloride, nitrate and mercury in the FADA ash sample were detected
in the SPLP leachate. No metals were detected in the 1971 ash basin leachate
sample that exceeded 2L or IMAC. Antimony, arsenic, cobalt, iron and
vanadium were detected in the FADA leachate sample at concentrations
exceeding the 2L or IMAC (Table 7-4).
Three ash samples were tested by Energy Dispersive X-Ray Fluorescence for
metal oxides (Table 7-5) and a suite of elements (Table 7-6). The sample from
the FADA and the shallow sample from the 1971 ash basin were comprised
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primarily of silicon dioxide (SiO2), aluminum oxide (Al2O3), and iron oxide
(Fe2O3), while the lower ash sample from the 1971 basin was comprised of silicon
dioxide, aluminum oxide and iron oxide.
Chemistry of Ash Pore Water 7.2.3
Two samples of ash pore water collected from ABMW-01S (1971 ash basin) and
ABMW-2S (FADA) were analyzed for the expanded list of COIs (Table 6-3).
Arsenic, manganese, and vanadium were detected in ash pore water samples
from both the 1971 basin and the FADA above the corresponding 2L or IMAC
(Table 7-8). Boron was also detected in the 1971 basin sample above 2L while
barium and iron were detected above the 2L in the FADA ash pore water.
Molybdenum, a metal for which a 2L Standard has not been assigned, was
detected in samples from both basins at a concentrations ranging from .005 to
0.190 mg/L.
Elevated concentrations of calcium, magnesium, sodium, bicarbonate and
chloride were also detected in the samples of ash pore water (Table 7-7).
Sorption characteristics (Kd) for arsenic, barium, boron, cobalt, iron, manganese,
selenium and vanadium are being determined for the ash. Results of these
analyses are pending and will be submitted in the CAP. Sorption factors are
being determined for these metals for the following reasons:
Arsenic, barium, boron, iron, manganese, and vanadium were detected
above the 2L or IMAC in ash basin pore water
Cobalt and selenium were detected above the 2L or IMAC in a sample
from one or more of the monitor wells.
The valence state, or chemical speciation, of arsenic, chromium, iron, manganese,
and selenium were determined for pore water from ABMW-1S and ABMW-2S
(Table 7-9).
Hydrology of the Ash Basins 7.2.4
Depth to water in the 1971 ash basin was measured at approximately 34 feet bgs
at an elevation of 11.16 above mean sea level (AMSL). The vadose zone in the
ash basin is comprised almost wholly of ash. The maximum thickness of the ash
is approximately 80 feet; therefore approximately 46 feet of ash are saturated.
The underlying natural ground surface consists of approximately one to two feet
of surficial sands underlain by fine sands and silts of the Pee Dee formation. The
water level in AMBW-1D, screened within the Pee Dee formation, is 10.55 AMSL,
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indicating a slight downward vertical gradient in the 1971 ash basin. The
downward head loss is 0.71 ft. over a distance of 46 feet, yielding a downward
vertical gradient of 0.0154 ft./ft. The top of the 1971 ash basin stack stands
approximately 20 feet above adjacent land grade; indicating the ash basin likely
serves as a recharge area to the surficial aquifer. Groundwater measurements
indicate the adjacent sand hills east of the basin are also acting as a recharge area.
No water level data was collected within the clay-lined 1984 basin; however
standing water is present on the north side of this basin.
The depth to water in the FADA is approximately two to three feet bgs at an
elevation of 7.42 feet AMSL. The ash thickness at ABMW-1S is approximately
eight feet; therefore at least five feet of the ash is saturated in the FADA. Due to
the low-lying ground in the FADA, this area can become flooded during periods
of heavy rain and the entire ash thickness would be saturated. The natural soil
beneath the ash in the FADA consists of surficial sands to a depth of
approximately 46 feet bgs. The ash-soil contact was observed to be saturated and
loose; indicating some perching of groundwater in the ash on the natural ground
surface below. The water level in the deep FADA well, ABMW-2D, was
measured at two to three feet bgs at an elevation of 7.39 AMSL, indicating a
downward vertical gradient in this area.
The drainage canal for the Site process water extends along the southern
boundary of the 1971 ash basin and likely intersects shallow groundwater and
controls the elevation at which groundwater flows from the 1971 ash basin to the
south (Figure 1-2). Also, the cooling pond located adjacent to the 1971 ash basin
to the west likely also serves as a recharge to the surficial aquifer and effects flow
in the zone from the ash basin.
The horizontal hydraulic conductivity of the ash in the screened interval of
ABMW-01 (1971 ash basin) was determined to be 1.5 x 10-4 cm/sec while the
hydraulic conductivity of the screened interval of ABMW-2S (FADA) was
determined to be 8.17 x 10-4 cm/sec (Appendix G). These values will be used as
an input to the Site groundwater model.
7.3 Piezometers and Seeps
No seeps were identified at the Site and no data from piezometers were collected
relative to the ash basins. Ash pore water infiltrates into the surficial aquifer below the
unlined ash basin.
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7.4 Constituents of Interest
COIs identified in conjunction with the Site ash basins include arsenic, boron, barium,
cobalt, iron, manganese, TDS, pH and vanadium. The ash pore water samples collected
from the pore water wells (Table 7-7) exceed the 2L or IMAC for these COIs with the
exception of cobalt. Three of the samples fell within the pH range of 6.5 to 8.5, while
one sample (ABMW-1S) exhibited a pH of 8.97during the second sampling event.
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8.0 SOIL AND ROCK CHARACTERIZATION
Soil borings were performed at each of the 16 new well locations to collect soil samples
from the unsaturated zone and the zone of saturation in areas outside of the ash basins.
These samples were analyzed for total metals, TOC, and leaching characteristics.
A total of 38 groundwater monitor wells were installed at 16 locations outside the ash
basins. Two or more wells were constructed at each location (with the exception of
AW-7, where a previously existing well served the purpose of the proposed well);
screened in the upper and lower surficial aquifer. At selected locations, an additional
one or two more wells were installed; within the upper and/or lower portion of the Pee
Dee Formation. The wells were installed to provide groundwater samples from the
following saturated zones:
Shallow intermediate zone
Lower surficial aquifer
Upper portion of the Pee Dee Formation
Lower portion of the Pee Dee Formation
Samples from these locations were analyzed to determine mineralogy, physical, and
chemical properties (Appendix F).
Rinse blanks from sample collection equipment were collected. Rinse blanks for most
soil samples were collected by pouring deionized water through the sonic drill bit.
COIs detected in these samples indicate that rust that collects on the bit overnight was
rinsed into the sample bottle. Although iron, cobalt and vanadium were detected in
several of the equipment blanks associated with the soil, the overall quality of the
sample data is not impacted. With the exception of iron, the constituents found in the
blank samples were either not detected in the associated soil and groundwater samples
or were detected at concentrations significantly higher than that found in the blanks.
Iron is commonplace in soils and groundwater at the Site and its detection in the
equipment blank samples is not considered to impact the overall quality of the sample
data (Appendix D).
Geologic cross-sections illustrating groundwater COI concentrations are presented as
Figures 8-1 and 8-2. Further discussion of groundwater sample results are presented in
Section 10 of this document. A map showing soil concentrations above applicable
comparison levels is presented in Figure 8-3.
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8.1 Background Soil
Soil samples collected from background locations are discussed in conjunction with
soils from the remainder of the Site in the following section. Shallow soils at
background locations AW-08 and MW-37 are similar to the surficial aquifer sands in
monitor wells outside of the basin.
Soils were tested in accordance with Work Plan Section 7.1.1. Physical property testing
of soil samples indicates that Site soils are predominately sand (Table 8-1), with the
exception of the silts identified in the lower Pee Dee formation.
Mineralogical determinations indicate that feldspar, calcite and clay minerals (kaolinite
and illite) accompany quartz in soil samples from the Site (Table 8-2). Dolomite was
detected in one sample.
Soils beneath the Ash Basin 8.1.1
The contact between the ash and underlying soils in the ash basin borings was
visually distinct. There was no visible evidence of substantial migration of ash
into underlying soils or mixing of ash with those soils.
Comparison of chemical analytical data for soils beneath the ash basin with the
chemistry of the ash as revealed in both total (Table 7-3) and leaching data
(Table 7-4) yields the following observations:
Aluminum, arsenic, barium, cobalt and selenium concentrations in the ash
are significantly higher than in the underlying soils, indicating that these
metals are relatively immobile.
Iron occurs in soils beneath the basin at concentrations significantly higher
than that at background and other soils outside the basin, indicating that
the ash could be a source of iron.
Vanadium concentrations in ash and soil are comparable (although soils
beneath the basin are consistently lower than ash), and leaching data
indicate that vanadium is relatively immobile.
Arsenic leaching results indicate that it should exhibit relatively high
mobility, but the presence of low levels of arsenic in soils beneath the
basin indicate moderate mobility.
Boron concentrations in ash and soils across the Site are below PSRG;
however, boron is present in many groundwater samples downgradient
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of the ash basins but not in background locations. These data indicate that
if the ash were the source of the boron, the leaching process is near
completion and that boron in solution in groundwater samples does not
precipitate or adsorb at appreciable levels in soil. SPLP data on ash
samples indicate concentrations below 2L.
Site Soils 8.1.2
With the exception of the soil samples collected from the ash basin borings, all
soil samples collected during the assessment were collected from near the Site
perimeter, with the exception of AW-8, which is located north of the compliance
boundary for the ash basins.
COIs detected above a Regional Screening Level (RSL) in the soil samples
include arsenic, iron manganese, vanadium, cobalt and boron. However, boron
and cobalt exceeded the RSL in only one sample from the Pee Dee formation and
manganese was detected in only two soil samples from the Pee Dee formation.
Vanadium was found in concentrations above the RSL in only three samples; all
collected from the Pee Dee formation.
Iron was the only COI to exceed RSL in samples collected from the surficial
aquifer and was detected in most samples with the notable exception of
upgradient location AW-08 and background location MW-37. Iron was also
detected in most Pee Dee samples.
Metal oxide analysis of soil samples (Tables 8-3, 8-4, 8-5, and 8-6 and Figure 8-1)
indicate that oxides of silicon (74 to 100 percent) and aluminum (1.3 to 5.4
percent) are the predominate chemicals present. Trace metal oxides (potential
COIs) detected in appreciable concentrations include iron (0.2 to 2.8 percent), and
manganese (non-detect to .02 percent).
All of the metals analyzed in SPLP leaching tests, with the exception of arsenic
and mercury were detected in leachate, or had estimated quantities, from one or
more soil sample. Review of these results indicates that aluminum, barium,
boron, iron, sodium and vanadium would be mobilized from natural soils at the
Site in the highest concentrations.
Surficial Soils 8.1.3
Soil samples from the surface to two feet bgs were collected at 14 locations. Iron
was the only COI detected above a soil screening level. These results are
discussed in greater detail in Section 12.2.5.
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8.2 Comparison of Results to Applicable Levels
Qualitative evaluation of the soil chemistry data suggest that, with the potential
exception of iron concentrations, soils beneath the ash basins, at AW-8 and at the
perimeter of the Site have not been greatly affected by the ash basins.
While there are numerous detections in soils of COIs above the RSL, other than iron,
these exceedances are detected only in the Pee Dee formation and only at three
locations, AW-6, AW-7 and SMW-6. Given the distance of these boring locations from
the ash basins and the lack of detection in soils of these COIs at other locations along
flow transects, it is questionable whether these exceedances can be attributed to
operation of the ash basin.
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9.0 SEDIMENT AND SURFACE WATER CHARACTERIZATION
Sediment and surface water samples were collected from seven locations beyond the
perimeter of the ash basin.
To provide information on surface water quality in the cooling pond and Cape Fear
River, with respect to the ash management area, seven surface water samples were
collected. Four samples, (SW-004, SW-8A, SW-6A, and SW-1C), were collected from the
cooling pond at the locations shown on Figure 1-2.
Three surface water samples (SW-CFUP, SW-CFP, and SW-CF001) were collected from
the Cape Fear River (Figure 1-2). These samples were collected during an outgoing
tide. SW-CFUP is considered an upgradient sample. SW-CPF was collected from the
makeup pump to the cooling pond, which is routinely sampled as part of the NPDES
permit. SW-CF001 was collected downgradient of NPDES Outfall 001.
Sediment samples were collected from the bed surface at each of the surface water
sample locations (Figure 1-2). The SW-CFUP location is considered a background
sediment sample. The sediment samples were analyzed for total inorganics, using the
same constituents list proposed for the soil and ash samples and pH, cation exchange
capacity, particle size distribution, percent solids, percent organic matter, and redox
potential.
Residential soil screening levels were exceeded in the sediment samples collected at
SW-CF001 and SW-CFP for iron, manganese and cobalt (Table 9-1). Iron was detected
at the highest concentrations; 11,700 mg/kg at SW-CR001 and 10,900 mg/kg at SW-CFP.
Detected concentrations of manganese were 226 mg/kg at SW-CF001 and 414 mg/kg at
SW-CFP. Cobalt was estimated at a concentration of 7.6 mg/kg in SW-CFP. An
estimated concentration of 4.6 mg/kg of arsenic was reported for SW-06A from the
cooling pond perimeter. Since these concentrations are often naturally- occurring and
their concentrations cannot be quantified within laboratory quality control limits, no
conclusion can be drawn related to these data. No other COIs were detected above
industrial or residential screening levels.
9.1 Comparison of Exceedances to 2B Standards
Exceedances of 2B concentrations were detected in the surface water samples for
aluminum, copper, and zinc. Aluminum and copper exceedances were detected at SW-
01C (cooling pond) and the SW-04 (cooling pond) sample exceeded the 2B concentration
for copper. The SW-CF001 (NPDES Outfall to river), SW-CFP (river sample) and the
SW-CFUP (upgradient river sample) samples exceeded the 2B concentration for
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aluminum. The SW-CFUP also exceeded the 2B concentration for zinc. The SW-06A
and SW-08A samples exceeded the 2B concentration for copper.
9.2 Discussion of Results for Constituents Without Established 2B
COIs for which a 2B concentration has not been established include boron, iron,
manganese, TDS, and vanadium (Table 9-3). Boron was detected at concentrations
ranging from 196 to 204 µg/L in the water samples collected from the cooling pond.
Boron was not detected in water samples collected from the Cape Fear River. Iron was
detected at a concentrations ranging from 49 µg/L to 127 µg/L in the cooling pond
samples and at concentrations ranging from 1,310 to 1,830 µg/L in the Cape Fear River
samples. Manganese was detected at a concentration of 7 µg/L in SW-01C from the
cooling pond and at concentrations ranging from 42 to 96 µg/L in samples collected
from the Cape Fear River. TDS was detected in a range of 89 to 150 µg/L in all surface
water samples. Vanadium was detected in all surface water samples at concentrations
ranging from 1.25 to 1.76 µg/L in the river samples and 3.04 to 3.87 µg/L in the cooling
pond samples.
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10.0 GROUNDWATER CHARACTERIZATION
Groundwater samples from the 42 new monitor wells and 29 existing monitor wells
were analyzed for the GAP COIs (Table 10-1). In addition, 28 wells, including
previously existing wells and new wells, were sampled for speciation of selected COIs.
A Comprehensive Analytical Results table is presented in Attachment 4.
10.1 Background Groundwater Conditions
MW-5C, located approximately 3,000 feet north of the ash basins, is considered the
background location for groundwater in the northern portion of the Site. MW-5C is
screened in the lower surficial aquifer. Concentrations of cobalt (1.62 µg/L) and
manganese (441 µg/L) were detected in MW-5C during compliance well sampling in
June, 2015. No other constituents exceeded 2L or IMAC in the MW-5C sample.
MW-4B has historically been used as a background well for the southern portion of the
Site. During the CSA, MW-37B/C were installed as an additional background wells in
the southern portion of the Site. Iron and manganese were detected at concentrations
exceeding 2L in MW-4B. Cobalt, iron and manganese were also detected above 2L or
IMAC in MW-37B and MW-37C and vanadium was detected above IMAC in MW-37C.
10.2 Discussion of Redox Conditions
Soil staining in the saturated zone which would indicate oxidizing conditions is present
in some portions of the lower the surficial aquifer. Reddish-orange layers of medium to
coarse sands were observed in the lower surficial aquifer in AW-9D, CUB-03 and CUB-
06 in the southeast portion of the Site and SMW-1C, SMW-4C, SMW-5C and SMW-6D,
east of the central portion of the Site.
The Pee Dee Formation exhibited evidence of reducing conditions that include gray
color and strongly negative ORP readings in groundwater. Strongly negative ORP
readings, as well as the presence of wood in quantities ranging from trace to a 2-foot
layer (AW-3C) are evidence of reducing conditions in some areas of the lower portion of
the surficial aquifer.
Valence speciation determinations were performed on groundwater samples from
monitor wells installed in 2015, compliance wells, and select existing wells along flow
transects outward from the ash basin (Table 10-3). General observations follow:
As+3 was the dominant species detected for each sample containing arsenic. The
sample from ABMW-2D, beneath the FADA, which contained the highest
concentration of total arsenic, was found to contain 119 µg/L of As+3 versus 7.71
µg/L of As+5.
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Hexavalent chromium was detected at concentrations comparable (same order of
magnitude) to the proposed California drinking water standard of 0.01 µg/L.
Reduced iron was the dominant species in each sample with the exception of
AW-06D in the Pee Dee Formation and SMW-03B in the surficial aquifer.
Mn+3 was the dominant species where manganese was detected with the
exception of the wells screened in the lower Pee Dee.
10.3 Regional Groundwater Data for Constituents of Potential
Concern
Iron, manganese, cobalt and vanadium are detected across the Site, including at the
background locations. It is anticipated that site specific background levels will be
calculated for these metals after eight sets of groundwater data are available.
NURE data on vanadium were discussed in Section 6.3.2 of this report. These data have
not been analyzed in detail, but they make it clear that vanadium is common in North
Carolina groundwater.
As previously referenced in Section 4.4.4, regional groundwater data indicate boron
concentrations in the Pee Dee Formation can be elevated. A well in Myrtle Beach which
is screened within the Pee Dee was found to contain 1,600 µg/L boron, likely due to salt
water intrusion, given the depth of the sample and the proximity to the coast.
10.4 Groundwater Analytical Results
Iron, boron and manganese were detected at the highest concentrations in the largest
number of wells across the Site. Cobalt and vanadium were also detected at
concentrations exceeding IMAC in a high number of wells, but at lower concentrations.
Figures 10-1 through 10-4 illustrate groundwater sample concentrations greater than 2L
or IMAC in wells installed within the upper surficial, lower surficial, Upper Pee Dee
and Lower Pee Dee aquifers, respectively. Geologic cross sections illustrating COI
analytical results are presented on Figure 8-1 and 8-2.
Iron is present in some background wells and in wells across the Site; however the
highest detected concentrations were in the FADA ash pore water well (29,200 µg/L).
Outside of the basin, the highest iron concentration was detected in off-site well SMW-
2B (28,800 µg/L). Elevated concentrations are present at most locations adjacent to, and
downgradient of the ash basins however, it is unclear that the high concentrations in the
off-site wells east of the Site are related to the ash basins, based on their distribution and
occurrence.
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The occurrence of high concentrations of iron is greater in the lower surficial aquifer.
Concentrations of iron are lower in the Pee Dee Formation wells. The occurrence of
detected concentrations of manganese over the 2L closely matches that of iron.
Cobalt was not detected in the ash pore water wells but was detected in the background
wells and several surficial aquifer wells, specifically along the eastern Site boundary
and off-site wells, where the highest concentrations were detected. Cobalt was only
detected in MW-15D, near the FADA. Based on these data, it is not clear that the
occurrence of cobalt is related to the ash basins. Cobalt has an IMAC of 1 ug/L.
Boron was detected in the 1971 ash pore water well but not in the FADA ash pore water
well. Boron was not detected in background wells. Boron is the most mobile of the
metals of concern (refer to Section 6.3.3), with lateral migration apparently more
prevalent than vertical movement. Elevated boron concentrations were also detected in
the Pee Dee Formation wells. However, the occurrence of boron in the lower Pee Dee
wells (AW-5E, AW-6E and MW-23E) is closely aligned with concentrations of chloride
over 2L. Chloride does not exceed 2L in any other well and its occurrence at that depth,
as well as that of boron and other metals may be attributed to salt water intrusion.
The detected boron concentration in Site Pee Dee Formation wells is comparable the
previously reference well in Myrtle Beach, South Carolina.
Arsenic has migrated limited distances vertically and horizontally from the ash basins
and is present above 2L in only the ash pore water wells and two surficial aquifer wells
near the ash basins.
Vanadium was detected in the ash pore water wells and in wells across the Site in both
the surficial and Pee Dee aquifers at concentrations exceeding IMAC. Vanadium was
detected in upgradient well AW-8B and background well MW-37B/C. The highest
concentration detected, 39.6 µg/L, in MW-20 between the FADA and the cooling pond
intake canal, is greater than other areas.
Selenium was detected in only two wells; well MW-27B located north of the 1984 ash
basin and AW-6D, a perimeter well screened in the upper Pee Dee. Thallium was
found to be above IMAC in four wells. It is not clear that it has migrated from the ash
basin as it was not detected in the ash pore water wells and only appears in a limited
number of wells at relatively low concentrations. The detected concentrations of
thallium are 0.506 µg/L or lower and the exceedances are limited to an area southeast of
the old ash basin (MW-7C, MW-19, MW-22 and MW-23).
Isoconcentration maps illustrate the distribution of COIs in the upper surficial aquifer,
(Figures 10-5 through 10-14), the lower surficial aquifer (Figures 10-15 through 10-24),
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wells screened in the Upper Pee Dee Formation (Figures 10-24 through 10-34) and wells
screened in the Lower Pee Dee Formation (Figure 10-35 through 10-44).
Samples from the upgradient wells AW-08B/C, the two ash pore wells ABMW-1S and
ABMW-2S, and the two monitor wells beneath the ash basins (ABMW-1D and ABMW-
2D) were analyzed for isotopes of uranium and radium (Attachment 5). Uranium-238
(U238) was detected in the both samples from the 1971 ash basin, ABMW-1S and ABMW-
1D. Uranium was not detected in the upgradient wells or the FADA wells.
Radium226 was detected in all samples except upgradient sample AW-8C and radium228
was detected in both wells beneath the ash basins (ABMW-1D and ABMW-2D). The
highest concentration of Ra226 was 1.65 picoCuries per liter (pCi/L) in the upgradient
well sample AW-8B, comparable to the 1.62 pCi/L in the sample from beneath the 1971
ash basin. Ra228 was detected at 2 pCi/L in ABMW-1D and 1.6 pCi/L in ABMW-2D.
Maps of groundwater analytical results related to detection monitoring constituents and
inorganic parameters as identified in the USEPA April 2015 Final Ruling 40 CFR Parts
257 and 261 (CCR Rule), including boron, calcium, chloride, conductivity, pH, sulfate,
and total dissolved solids are included as Figures 10-45 through 10-48. Maps of
groundwater analytical results related to assessment monitoring constituents as
identified in the USEPA April 2015 Final Ruling 40 CFR Parts 257 and 261, including
aluminum, antimony, arsenic, barium, beryllium, cadmium, chromium, copper, iron,
lead, manganese, mercury, molybdenum, selenium, sulfate, sulfide, thallium, and
vanadium are included as Figures 10-49 through 10-52.
All the CCR rule constituents were not monitored as part of the CSA and therefore
maps for all CCR constituents are not provided.
Distributions of major cations and anions in ash pore water and the surficial and Pee
Dee monitor wells plotted on Piper diagrams provide an indication of the
characteristics of each zone. Ash pore water is dominated by calcium, magnesium, and
carbonate. The sulfate content of the ash pore water is lower than would be anticipated
(Figure 10-53). Ion ratios vary substantially in the surficial zone across the Site, but are
generally higher in calcium and magnesium, with AW-01B in the northeast portion of
the Site and SMW-4C off-site to the east being clear outliers (Figure 10-56). Major ion
ratios in samples from the Pee Dee are dominated by sulfate, chlorides, sodium and
potassium with outlier ABMW-1D, which is in the upper Pee Dee, beneath the 1971 ash
basin having a higher calcium and magnesium content and lower sodium and
potassium (Figures 10-53 and 10-58). Variations of constituent concentrations through
time are illustrated in Appendix H.
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Interwell prediction limits (parametric, nonparametric, and Poisson) were used to
compare background well data to the results for the most recent sample data from
compliance wells. Based on recommendations from ASTM (2012) guidance and USEPA
(2007), nondetected values were replaced with half of the detection limit for the
parametric and Poisson prediction limit procedures, and the detection limit for the
nonparametric prediction limit procedure.
Confidence levels were set at 99 percent for the parametric and Poisson prediction
interval. Confidence levels for the nonparametric prediction limit are given by n/(n+k)
were n is the number of background samples and k is the number of comparisons. The
false positive rate is given by 1-[n/(n+k)]. The number of comparisons is defined by the
number of recent sample dates multiplied by the number of compliance wells
(background wells).
Prior to conducting the interwell statistical analysis, the data set was “screened” and
“treated.” The Shapiro-Wilks goodness-of-fit test was used to evaluate the statistical
distribution of data sets because they contain less than 50 measurements. Each data set
was initially tested to determine whether the distribution is normal. If a data set fails
the test of normality, the natural logarithms of the data are taken and the procedure is
repeated. If the transformed data passes, the data set is designated as lognormal. If a
log transformed data set fails the test of normality, the data set is designated as non-
normal.
The parametric prediction limit was used to analyze data that were normally or log
normally distributed with less than or equal to 50 percent nondetects (ASTM D6312-98,
Section 6.1.1). The nonparametric prediction interval test was performed on normal
and lognormal data sets with greater than 50 percent nondetects and for data sets with
non-normal distributions with fewer than 90 percent nondetects (ASTM D6312-98,
Section 6.1.1). The nonparametric prediction limit compares each individual
downgradient concentration for the selected dates to the maximum concentration in
background samples. The Poisson prediction limit statistic was utilized to evaluate data
with greater than 90 percent nondetects (ASTM D6312-98, Section 6.1.1). Rinse blanks
from sample collection equipment were collected as summarized in Appendix C.
Although various constituents were detected at low level concentrations in several of
the equipment blanks associated with the groundwater samples as well as a number of
the filter blanks, the overall quality of the sample data is not impacted. The constituents
found in the blank samples were either not detected in the associated soil and
groundwater samples or were detected at concentrations significantly higher than that
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found in the blanks. The single exception being iron, commonplace across the Site and
its detection in equipment blanks is not considered to significantly impact the data.
Rinse blanks from the pumps and filters used to collect groundwater samples yielded
negligible detections of COIs (Appendix D).
10.5 Comparison of Results to 2L Standards
Twelve metals were detected in groundwater samples above 2L or IMAC; antimony,
arsenic, barium, boron, chromium, cobalt, iron, lead, manganese, selenium, thallium,
and vanadium (Table 10-2). Of the twelve metals exceeding 2L or IMAC, cobalt, and
manganese were detected in background wells MW-5C and MW-37B/C and iron was
detected in background wells MW-37B/C. Vanadium was detected above IMAC in
background well MW-37C. Only arsenic, barium, boron, iron, manganese and
vanadium were detected above 2L or IMAC in the ash pore water.
Lead was detected at a concentration of 16 µg/L in one well, AW-01B, located
approximately 3,600 feet northeast of the 1971 ash basin in the first sampling event but
was below detection limits for all other wells in both the first and second sampling
events. Lead was not detected in AW-01B during the second sampling event. The
turbidity during the first sampling event at AW-01B was 249 Nepthalic Turbidity Units
(NTUs) but was 9.87 during the second sampling event. Based on these data, the
detection of lead in AW-01B during the first sampling event is an anomaly related to
turbidity and therefore lead is not considered a COI at this Site.
Chloride was detected above 2L in the three deep Pee Dee Formation wells at
concentrations ranging from 490 to 540 mg/L. These concentrations are twice those
detected in the upper Pee Dee Formation wells and much greater than those detected in
the surficial aquifer wells and ash pore water wells. It is likely that the exceedance of
chloride in the lower Pee Dee wells represents salt water intrusion and is not
representative of Site conditions; chloride is not considered a COI. Additionally, the
detected concentrations of boron in the lower Pee Dee wells are significantly greater
than those detected in upper Pee Dee and surficial wells at the same locations. These
data may indicate that the detected concentrations of boron in the lower Pee Dee wells
may also be representative of salt water conditions. Regional groundwater data
supports this. A well located in Myrtle Beach South Carolina and screened from 95-105
feet within the Pee Dee formation was reported to contain a concentration of 1,600 µg/L
of boron. (Ground-Water Quality Data From the Southeastern Coastal Plain, Mississippi,
Alabama, Georgia, South Carolina, and North Carolina, Roger W. Lee, U. S. Geological Survey,
Open File Report 84-237, 1984).
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Selenium was detected in only two wells; well MW-27B located north of the 1984 ash
basin and AW-6D, a perimeter well screened in the upper Pee Dee. The detected
concentrations were slightly above 2L in each instance. The selenium detection in AW-
6D is an anomaly in that the laboratory reported a dissolved concentration above 2L but
a total concentration below detection limits. Additionally, AW-6D was sampled three
times and the selenium concentration was reported below the detection limit in two of
the three samples. Based on these data, the occurrence of selenium in these wells
appears to be unrelated to the ash basins and is therefore not currently considered a
COI. However, since MW-27B has historically contained selenium concentrations
above 2L and it may be influenced by radial flow from the adjacent 1984 ash basin.
Since no data is available for the 1984 ash pore water, it cannot be conclusively
eliminated as a source of selenium detected in MW-27B. Collection of additional data
for selenium has been identified as a data gap that does not compromise the
preparation of the CAP.
Total dissolved solids (TDS) exceeded 2L in the 1971 ash basin pore water well, in the
upper surficial aquifer well AW-01B, in the lower surficial well MW-31C and in Pee Dee
Formation wells AW-2D, AW-5E, AW-6D/E, AW-9D, MW-23E and SMW-6D. TDS is
considered a COI based on these data.
Levels of pH outside the 2L range were measured in most of the Site wells. The ash
pore water well, ABMW-1S and several of the Pee Dee wells had pH levels above 8.5
while most surficial wells had pH levels below 6.5.
Exceedances of 2L or IMAC for iron, cobalt, manganese, and vanadium are most
common across the Site (Figures 8-1, 8-2, 10-1, 10-2, 10-3, and 10-4). Each is naturally
occurring and common in shallow wells in this hydrogeologic setting. In most cases for
iron comparison of total concentrations to a corresponding “dissolved” (filtered)
concentration indicates that iron is associated with solids. Site specific background
concentrations need to be calculated for these COIs.
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11.0 HYDROGEOLOGICAL INVESTIGATION
Results of the hydrological investigation summarized in this section are the primary
components of the SCM.
11.1 Hydrostratigraphic Layer Development
The surficial aquifer and the Pee Dee Formation are the two distinct hydrostratigraphic
layers discussed in this assessment report. These aquifers are each composed of Coastal
Plain sediments. The saturated portion of the ash basins are superimposed on the
surficial aquifer. The 1971 ash basin area was excavated to a depth of approximately 40
feet bgs, effectively replacing the upper and lower surficial aquifer in this location.
Given the difference in ash and surficial soil hydraulic conductivities, it is likely the ash
serves as an interruption to flow within the surficial aquifer. The FADA ash thickness
extends to only eight feet bgs but is saturated at three feet bgs and is considered part of
the upper surficial aquifer flow zone.
Published data had indicated that the surficial aquifer, was of an average thickness of 35
feet, and was underlain by the Castle Hayne confining unit, with an average thickness
of 20 feet. The Castle Hayne aquifer was reported to have an average thickness of 60
feet in the northern Wilmington area. Additionally, the Pee Dee confining unit was
reported to underlie the Castle Hayne aquifer and have an average thickness of 10 feet
and mark the upper limit of the Pee Dee Formation. Previous studies by Catlin
Engineers (2010) and Geosyntec (2014) (Attachment 1) did not confirm the presence of
the Castle Hayne aquifer or the confining unit of the Pee Dee formation.
Eight borings performed for this assessment extended to a depth of 100 feet bgs and
three extended to a depth of 150 feet bgs. Neither the Castle Hayne confining
unit/aquifer nor the Pee Dee confining unit were encountered. Additionally, 10 soil
borings were extended to the top of the Pee Dee formation in the southeastern portion
of the Site in an effort to identify a confining unit. No confining unit was identified
during this assessment. The surficial aquifer lies unconformably over the fine sands
and silts of the upper Pee Dee formation at the Site.
11.2 Hydrostratigraphic Layer Properties
Groundwater analytical results from the assessment plotted on the geologic cross-
sections illustrate the properties of these layers (Figures 11-1 through 11-4).
Confining Unit 11.2.1
Previous reports and published data indicated that a confining unit was present
in the upper portion of the Pee Dee Formation. No confining unit was identified
at the Site during this assessment. In addition to monitor well borings that
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extended into the Pee Dee formation, 10 soil borings, designated Confining Unit
Borings (CUB) were installed in the southeastern and southern portions of the
Site for the purpose of locating the confining unit. These borings generally
encountered the same conditions as the monitor well borings; a sharp contact
between the lower surficial aquifer and the Pee Dee Formation with the poorly
sorted sands of the surficial directly overlying the dark gray/green fine sands and
silts of the Pee Dee.
In-Situ Tests 11.2.2
No in-situ tests were conducted except for slug tests.
Slug Tests 11.2.3
Slug testing is described in Section 6.2.3 and summarized in Table 6-7. Slug
testing indicates mean hydraulic conductivity values of 3.69 x 10-4 cm/sec within
the ash basin and 5.13 x 10-2 cm/sec within the surficial aquifer. Hydraulic
conductivity values were considerably lower in the upper Pee Dee wells (2.75 x
10-5 cm/sec) and lower still in the lower Pee Dee wells (4.56 x 10-7 cm/sec).
Porosity 11.2.4
No porosity tests were performed due to the inability to collect undisturbed
samples of the loose sands of the surficial aquifer; however a porosity value of
25-50 percent was used based on published dated (Fetter, Applied Hydrogeology,
Fourth Edition). The porosity values for the upper Pee Dee were determined to be
41.4 – 42.5 percent in the upper portion (45 – 50 ft. bgs) of the Pee Dee and 30.1
percent in a lower portion (99 ft. bgs).
11.3 Groundwater Flow Direction
Measurements in groundwater wells indicate overall flow is to the east and south
(Figures 6-6 through 6-8). Groundwater at the Site flows radially from the ash basin
and sand hills in the central portion of the Site. The cooling pond, which has a level
approximately 10 feet above the adjacent Cape Fear River, provides additional head to
the surficial aquifer.
The current interpretation of groundwater flow indicates a groundwater divide or ridge
east of the ash basin. Groundwater appears to flow in all directions from this ridge but
primarily to the east, west and south. The 1971 basin appears to act as somewhat of a
groundwater sink. This area was excavated to a depth of approximately 40 feet bgs
prior to placement of the ash. The original topography of the Site suggests that natural
groundwater flow in the ash management areas would have been to the west and
southwest toward a former creek and the river beyond. Groundwater to the east and
south of the groundwater divides flows east and south. The highest groundwater
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elevation at the Site was recorded in MW-5C to the north and the lowest was recorded
in MW-37B to the south; indicating a regional north to south flow direction.
The potential interferences from the off-site municipal, industrial production wells (and
the potential extraction wells) and Site production wells will be considered in the
groundwater flow model is being prepared for the CAP. As the model is being
prepared additional groundwater and surface water elevation monitoring may be
conducted.
11.4 Hydraulic Gradient
The horizontal hydraulic gradient from the ash basin to surrounding areas ranges from
0.000091 to 0.001 foot per foot (Table 6-8).
11.5 Groundwater Velocity
Groundwater velocities calculated for the four flow paths described in Section 6.2.2.
range from 0.185 to 8.55 feet per year. Slug tests that were conducted in wells screened
below the ash basin were analyzed for hydraulic conductivity and were used to
calculate the flow velocity. Flow rates from the ash basins to surrounding areas are the
highest due to the hydraulic gradient from the elevated basins to the surrounding areas.
11.6 Contaminant Velocity
Site specific sorption coefficients are being determined by the UNCC laboratory. While
not included in this report, site specific sorption coefficients will be available for
incorporation into the groundwater modeling that will be performed for the CAP. COIs
are expected to migrate at rates lower than groundwater velocity. Boron is likely an
exception to this generalization.
11.7 Characterization of COI Distribution
Distributions of COIs from the ash basin to the surrounding area are illustrated on the
primary flow transect (Section B-B’). Horizontal distribution is generally to the
east/southeast.
11.8 Groundwater / Surface Water Interaction
Due to the shallow groundwater table and the porous nature of the surficial aquifer
sediments, interaction between the cooling pond and canals is expected to be rapid with
these surface water bodies loading the underlying surficial aquifer.
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12.0 SCREENING-LEVEL RISK ASSESSMENT
Potential risks to human health and the environment have been assessed in accordance
with applicable federal and state guidance, as described in Section 8 of the Proposed
Groundwater Assessment Work Plan to support the groundwater assessment and
inform corrective action decisions, (SynTerra December 2014). Screening level human
health and ecological risk assessments have been performed to serve as the foundation
for evaluating potential risks to human and ecological receptors at the Site. NCDENR
has managed sample collection from nearby private water supply wells. Data from
these samples are contained in Appendix B.
Preliminary constituents of potential concern (COPCs) have been identified based on
evaluations performed in accordance with NCDENR recommendations regarding coal
ash constituents. Both screening level risk assessments compare maximum constituent
concentrations to appropriate risk-based screening values as a preliminary step in
evaluating the potential for unacceptable risks to potential receptors.
The screening-level risk assessment is not designed to characterize the horizontal
and/or vertical extent of potential impact, but rather to identify coal ash related
constituents that exceed published human and/or ecological health screening criteria
and warrant further consideration with respect to corrective action.
12.1 Human Health Screening
Introduction 12.1.1
This screening level human health risk assessment (HHRA) has been prepared in
accordance with Section 8 of the Proposed Groundwater Assessment Work Plan
(SynTerra 2014) and USEPA guidance for human health risk assessment,
including the USEPA Region 4 2014 Draft Final Human Health Risk Assessment
Supplemental Guidance, as applicable.
Conceptual Exposure Model 12.1.2
Consistent with standard risk assessment practice for developing conceptual
models, separate Conceptual Exposure Models (CEMs) were developed for on-
site human health evaluations. Figure 12-1 has been prepared illustrating
potential exposure pathways from the source area to possible human receptors.
The information in the CEM has been used in conjunction with the analytical
data collected as part of the CSA.
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The human health CEM is based on characterization of primary and secondary
sources and corresponding release mechanism from the sources. COPCs are
identified for environmental media affected by primary and secondary sources
as well as their potential routs of migration and transport to potentially exposed
on-site populations (receptors). Figure 12-1 identifies the source and release
mechanisms for the Site along with exposure medium and route. Potential
receptors at the Site are identified, with consideration of current land use
scenarios. The individual components of the human health CEM are further
described in the following sections.
Primary Constituent Source
The primary source of Site related constituents in groundwater is historical coal
ash management conducted in the FADA, 1971 Ash Basin, and the 1984 Ash
Basin. Groundwater, soil, surface water and sediment in the vicinity of these
sources that contain Site related constituents serve as an exposure medium.
Primary Release and Transport Mechanisms
Consistent with focus of this assessment on migration of ash basin constituents
into water, the primary potential constituent release and transport pathways at
the Site are as follows:
Desorption of coal ash constituents to coal ash pore water;
Infiltration of coal ash pore water to underlying groundwater;
Discharge of coal ash pore water to the cooling pond (Lake Sutton)
followed by discharge to the Cape Fear River via the NPDES permitted
outfall.
Secondary Release Mechanisms
The secondary potential constituent release and transport pathways at the Site
are as follows:
Transport of coal ash constituents in groundwater to sediments and
Transport of coal ash constituents in sediments to surface water.
Exposure Medium, Pathways and Exposure Routes
The exposure medium includes potentially impacted groundwater, soil, surface
water and sediments.
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The exposure routes associated with the potentially completed exposure
pathways evaluated for the Site include ingestion, inhalation and dermal contact
of environmental media.
12.1.2.1 Current/Future Recreational Fisherman
The potential exists for current and/or future fisherman on Lake Sutton to
be exposed to COPCs at the Site. This exposure scenario is considered in
the risk screening.
12.1.2.2 Current/Future Recreational Swimmer
The potential exists for current and/or future swimmer in Lake Sutton to
be exposed to COPCs at the Site. This exposure scenario is considered in
the risk screening.
12.1.2.3 Current/Future Recreational Hunter
The potential exists for current and/or future hunter to be exposed to
COPCs at the Site. This exposure scenario is considered in the risk
screening.
12.1.2.4 Current/Future Industrial Worker
The potential exists for current and/or future industrial workers to be
exposed to COPCs at the Site. This exposure scenario is considered in the
risk screening.
12.1.2.5 Future Resident
The potential exists for future residents to be exposed to COPCs at the
Site. This exposure scenario is considered in the risk screening.
Risk-Based Screening Levels 12.1.3
The human health risk assessment includes an initial comparison of constituent
concentrations in various media to risk-based screening levels. A comparison of
constituent concentrations in various media to the following risk-based screening
levels is presented in the following sections. The screening criteria include
chemical-specific screening levels based on concentrations that are Applicable or
Relevant and Appropriate Requirements (ARARs) [e.g., Safe Drinking Water Act
maximum contaminant levels (MCLs)] and concentrations resulting from risk -
based calculations that set concentration limits using carcinogenic or systemic
toxicity values under specific exposure conditions. These include:
Coal Ash Constituents – Regional screening level (RSLs) for soil
protective of groundwater and human health under residential-use
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scenarios and industrial-use scenarios (USEPA Regional Screening Levels
(RSLs) rev., June 26, 2015).
Coal Ash Pore Water - NCDENR Title 15A, Subchapter 2L.
Groundwater - NCDENR Title 15A, Subchapter 2L Standards, Interim
Maximum Allowable Concentrations (IMACs; 15A NCAC 02L.0202), and
USEPA Screening Level for Hexavalent Chromium in Residential Tap
Water (USEPA Regional Screening Levels (RSLs) rev., June 26, 2015).
Soil and Sediments - USEPA Residential and Industrial Soil Regional
Screening Levels (RSLs) Target Cancer Risk 1x10-6/Target Hazard Quotient
of 0.1 (USEPA Regional Screening Levels (RSLs) rev., June 26, 2015).
Surface Water - North Carolina Surface Water Standards (Subchapter 2B) and
USEPA National Recommended Water Quality Criteria for Human Health for
the consumption of water and organisms (NCDENR,
http://portal.ncdenr.org/web/wq/ps/csu/swstandards, Triennial Review; USEPA
National Recommended Water Quality Criteria; 2004).
Soil, sediment and groundwater will be compared to background data from
available local, regional and national background sediment, soil and ground
water data, as available.
Coal Ash and Coal Ash Pore Water
Coal ash and water retained within the FADA and ash basins are the sources of
constituents addressed by this risk screening process. Constituents impacting
groundwater from other onsite sources, offsite sources, or naturally occurring
sources, may be acknowledged, but are beyond the scope of this risk screening
process. Consequently, COPCs going forward will be attributable only to the
coal ash.
Coal Ash
Coal ash COPCs are, by definition, constituents of coal ash. Three ash samples
were collected from two borings installed within the Site ash basins. The coal
ash samples were analyzed for 28 inorganic constituents and total organic carbon
(TOC). Coal ash analytical results are summarized in Table 7-3 and compared
with constituent soil regional screening levels (RSLs) derived for the protection
of groundwater as well as the protection of human health under residential-use
and industrial-use scenarios. Constituents that have at least one soil screening
criteria and were detected at concentrations below all applicable RSLs, or were
not detected and their analytical method detection limits where below their
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respective RSLs, may not be considered a coal ash COPC. Coal ash constituents
that may not be coal ash COPCs are listed below:
Antimony Molybdenum
Boron Nickel
Cadmium Strontium
Total Chromium Thallium
Manganese Zinc
Conversely, the following coal ash constituents are retained as preliminary coal
ash COPCs for the reasons indicated (Table 7-3):
Coal Ash Constituent Concentrations
Greater Than One Or More Soil RSLs
Coal Ash Constituents
That Have No Soil RSLs
Aluminum
Arsenic
Beryllium
Cobalt
Copper
Iron
Lead
Mercury
Selenium
Vanadium
Calcium
Chloride
Magnesium
Nitrate (as N)
Potassium
Sodium
Sulfate
TDS
Coal Ash Pore Water
Coal ash pore water is precipitation that has infiltrated through the coal ash and
is retained within an ash basin. Coal ash pore water above the ash/soil interface
results in saturated conditions within disposed ash. Desorption of coal ash
constituents into precipitation that has infiltrated into the coal ash is expected to
be greatest wherever the coal ash is under saturated conditions for extended
periods of time. The coal ash pore water and solubilized inorganic constituents
will eventually infiltrate into the underlying groundwater. Consequently, coal
ash pore water can potentially impact groundwater quality when solubilized
inorganic constituents are present at concentrations above 2L or IMAC.
Conversely, solubilized inorganic constituents present in ash pore water at
concentrations below 2L or IMAC do not pose unacceptable risk to the quality of
underlying groundwater.
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A total of five coal ash pore water samples were collected from two monitoring
wells screened within the coal ash. Ash pore water samples were analyzed for
28 inorganic constituents. Analytical results of ash pore water analyses are
presented in Table 12-1 along with constituent 2L or IMAC, where applicable.
The coal ash pore water samples and constituents that exceeded a 2L or IMAC
are identified in Figure 12-2.
An ash pore water constituent that has a 2L or IMAC and is detected at a
concentration below its 2L or IMAC, or was not detected and its analytical
method detection limit is below its 2L or IMAC, is not a coal ash COPC because it
do not pose an unacceptable risk to the quality of underlying groundwater. Site
coal ash constituents that meet these conditions are listed below:
Antimony Mercury
Beryllium Nickel
Cadmium Nitrate (as N)
Chloride Selenium
Total Chromium Sulfate
Cobalt Thallium
Copper Zinc
Lead
Conversely, a coal ash constituent that exceeds its groundwater screening criteria
or has an analytical method detection limit greater than its groundwater
screening criteria, or has no groundwater screening criteria may adversely affect
the quality of underlying groundwater. The following Site coal ash constituents
are retained as preliminary coal ash COPCs for the reasons indicated:
Coal Ash Constituent
Concentrations Greater
than 2L or IMAC
Coal Ash Constituents
that have no 2L or IMAC
Arsenic
Barium
Boron
Iron
Lead
Manganese
TDS
Vanadium
Aluminum
Calcium
Magnesium
Molybdenum
Potassium
Sodium
Strontium
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Calcium/Magnesium/Potassium/Sodium
Calcium, magnesium, potassium, and sodium analyses were conducted for the
purpose of characterizing the geochemistry of different aquifers. These
constituents are found in abundance in natural groundwater systems and are
routinely quantified by geochemists to generate piper diagrams or plots of major
cations and anions. Cation and anion data collected has been used to generate
piper diagram plots that categorize geochemical characteristics of the coal ash
pore water, the surficial aquifer, and the Pee Dee Formation (Section 10).
Furthermore, these naturally occurring constituents do not pose unacceptable
risks to human health when present in groundwater at moderate concentrations.
This is one reason why these constituents have no established numerical limits
(e.g., 2L, IMACs, Safe Drinking Water Act MCLs) in groundwater for the
protection of human health. Calcium, the most abundant mineral in the body, is
found in many foods and is available as an over-the-counter dietary supplement.
Likewise, magnesium, potassium and sodium are also present in many common
foods and are also available as, or included in, over-the-counter dietary
supplements. Although calcium, magnesium, potassium and sodium are coal
ash constituents, it is unlikely that they will be significant contributors to
potential human health risk posed by coal ash constituents. For these reasons,
calcium, magnesium, potassium and sodium will not be considered coal ash
COPCs (Table 12-2).
Coal Ash COPC Determination
Coal ash COPC determinations are summarized in Table 12-2 along with the
rationale for the determination. Constituents that are coal ash COPCs will be
evaluated as to whether they are groundwater, soil, sediment or surface water
COPCs that are potentially attributable to coal ash. Constituents that are not coal
ash COPCs will not be evaluated going forward.
Groundwater
Site groundwater meets the definition of Class GA groundwater (15A NCAC
02L.0201). Consequently, the 15A NCAC 02L.0202 and IMAC groundwater
quality values (2L or IMAC) apply. The concentrations of groundwater
constituents that have 2L or IMAC are compared to those screening criteria.
Groundwater constituents having concentrations below their respective 2L or
IMAC in all groundwater samples do not pose an unacceptable risk to human
health. Groundwater constituents having concentrations above their respective
2L or IMAC warrant further evaluation. The source of groundwater constituents
detected above 2L or IMAC could be naturally occurring conditions (e.g.,
elevated metals in saturated subsurface matrix), high turbidity groundwater
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samples, an offsite contaminant release, the coal ash, or other site related source
of groundwater constituents. A constituent that exceed its 2L or IMAC or has no
2L or IMAC and is a coal ash COPC will be a designated groundwater COPC
potentially attributable to coal ash. Conversely, a constituent in groundwater
that exceeds its 2L or IMAC or has no 2L or IMAC but is not a coal ash COPC
will not be a groundwater COPC potentially attributable to coal ash.
The following groundwater constituents are not groundwater COPCs potentially
attributable to coal ash because they are not coal ash COPCs (Table 12-2):
Antimony
Beryllium
Cadmium
Calcium
Chloride
Total Chromium
Cobalt
Copper
Lead
Magnesium
Mercury
Molybdenum
Nickel
Nitrate (as N)
Potassium
Selenium
Sodium
Strontium
Sulfide
Thallium
Zinc
Groundwater wells were sampled in February, March, April, and/or June 2015.
The following field parameters were monitored and recorded during sampling:
pH (s.u.)
Temperature (OC)
Specific Conductivity (µS/cm)
Water Level (ft. below TOC)
Dissolved Oxygen (DO; mg/L)
Turbidity (ntu)
Oxidation/Reduction Potential
In addition, ferrous iron concentration (mg/L) in groundwater was estimated
using a colorimetric field screening procedure.
Field parameters and analytical results are assimilated on risk assessment
screening Tables 12-1, 12-3, 12-4 and, 12-5. In addition, groundwater analytical
results are evaluated against the 2L or IMAC, where applicable.
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Background Groundwater
There are two water bearing units associated with the Site groundwater
assessment; the surficial aquifer and the Pee Dee Formation. There are four
groundwater monitor wells (MW-4B, MW-05C, MW-37B, and MW-37C)
monitored for background conditions within the surficial aquifer. No
background wells have been installed within the Pee Dee Formation.
Background wells for the surficial aquifer and the analytical results of
background groundwater samples collected in 2015 are provided on Table 12-1.
Included in Table 12-1 are statistical metrics (number of samples analyzed,
number of detections, average (statistical mean – detections only) constituent
concentrations, and maximum constituent concentration and comparisons of
constituent concentrations to the respective 2L or IMAC.
Background Groundwater – Surficial Aquifer
Analytical results of groundwater samples collected in 2015 from the surficial
aquifer background wells indicate that the following constituents were detected
at concentrations above respective 2L or IMAC:
Cobalt
Iron
Manganese
Vanadium
Cobalt was detected above the IMAC (1 µg/L) in at least one groundwater
sample collected from each of the four background groundwater monitor wells
in 2015. The initial groundwater sample collected from MW-37B in March 2015
contained no cobalt above the detection limit (<1 µg/L); however, cobalt was
detected at a concentration of 2.52 µg/L during confirmation sampling conducted
in June 2015. Similarly, the initial groundwater sample collected from MW-37C
in March 2015 contained cobalt a concentration of 2.99 µg/L; however, cobalt was
not detected above the detection limit during confirmation sampling conducted
in June 2015. This inconsistency of cobalt detections in groundwater samples
collected from background monitor wells suggest that further confirmation
sampling is warranted.
To date, iron concentrations at the four background wells have been inconsistent.
Iron was detected above the 2L (300 µg/L) in 4 out of the 9 background
groundwater samples collected in 2015. Iron concentrations in both groundwater
samples collected from MW-37B (687 µg/L 9,580 µg/L) were above the 2L;
however, iron concentrations were 13 µg/L or below in the three groundwater
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samples collected from MW-05C. Furthermore, the iron concentration in the
MW-37C March 2015 groundwater sample was 9,500 µg/L however the iron
concentration in the MW-37C June 2015 groundwater sample was 33 µg/L.
Similarly, the iron concentration in the AW-04B February 2015 groundwater
sample was 2,600 µg/L however the iron concentration in the AW-04B June 2015
groundwater sample was 41 µg/L.
Manganese was detected in all surficial aquifer background samples collected in
2015 with 6 out of 9 samples exceeded the 2L (50 µg/L). Manganese
concentrations in two samples collected from MW-05C were in relatively
consistent range (441 – 535 µg/L). In contrast, the manganese concentration in
the MW-37B March 2015 groundwater sample was 38 µg/L; however, the
manganese concentration in the MW-37B June 2015 groundwater sample was 254
µg/L. Similarly, the manganese concentration in the MW-37C March 2015
groundwater sample was 233 µg/L however the manganese concentration in the
MW-37C June 2015 groundwater sample was 6 µg/L.
Vanadium was detected above the IMAC (0.3 µg/L) only in background well
MW-37C. Vanadium concentrations in two samples collected from MW-37C
were 1.15 µg/L and 1.22 µg/L. Vanadium was not analyzed in the MW-05C
groundwater samples and vanadium concentrations were below the detection
limit (0.3 µg/L) in the MW-37B groundwater samples.
Speciation analysis was conducted on groundwater samples collected from
background well MW-05C (Table 10-3). The concentration of hexavalent
chromium Cr(VI) was 0.019 µg/L. The EPA screening level for hexavalent
chromium in residential tap water is 0.035 µg/L (USEPA RSLs; rev., June 26,
2015).
Downgradient Groundwater – Surficial Aquifer
Analytical results of surficial aquifer downgradient groundwater samples
collected in 2015 are presented in Table 12-4. The following constituents were
detected at concentrations above respective 2L or IMAC or do not have a
groundwater screening value protective of human health:
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Surficial Aquifer COPC
Potentially Attributable To Coal Ash Not A Coal Ash COPC(1)
Aluminum
Arsenic
Boron
Iron
Manganese
TDS
Vanadium
Cobalt
Lead
Nitrate (as N)
Selenium
Thallium
Note (1): See Table 12-2
Aluminum is a coal ash COPC because it is in coal ash at concentrations greater
than soil RSL (Table 7-3) but is not included in the 2L or IMAC. Aluminum was
detected in 85 out of 86 downgradient surficial aquifer groundwater samples at
concentrations ranging from <5 µg/L to 18,300 µg/L. Aluminum may be
eliminated as a surficial aquifer COPC if it can be demonstrated that it is
naturally occurring or a site-specific groundwater criteria protective of human
health is developed for aluminum. Until then, aluminum is a surficial aquifer
COPC potentially attributable to coal ash.
Arsenic concentrations were below the detection limit (1 µg/L) in 85 out of 104
surficial aquifer groundwater samples analyzed. Of the 19 samples having
quantifiable arsenic concentrations, only 5 of the samples collected from ABMW-
2D, MW-15, and MW-21C had arsenic concentrations above the 2L (10 µg/L).
These wells are in close proximity of the FADA or the 1971 ash basin (Figure 2-1)
and are screened at similar depth intervals. Arsenic is a surficial aquifer COPC
potentially attributable to coal ash.
Boron was not detected above the analytical detection limit (<50 µg/L) in seven
background samples but is in ash pore water and the surficial aquifer. Boron
was detected in 63 out of 104 surficial aquifer groundwater samples collected in
2015. Twenty-one of the 63 surficial aquifer groundwater samples collected from
10 wells contained concentrations of boron above the 2L (700 µg/L). In every
instance, these wells were sampled at least twice and boron concentrations were
confirmed to be above the 2L with the minimum, average, and maximum boron
concentrations being 776 µg/L (SMW-01C), 1,628 µg/L (statistical
mean/detections only), and 3,060 µg/L (MW-23C), respectively. Boron in ash
pore water collected from ABMW-01S (1971 Ash Basin) ranged between 3,940 –
3,690 µg/L whereas boron in ash pore water collected from ABMW-02S (FADA)
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ranged between 222 – 234 µg/L. Boron is a surficial aquifer COPC potentially
attributable to coal ash.
Surficial aquifer groundwater samples were analyzed for total (CrIII plus CrVI)
chromium. Eight out of 104 samples analyzed contained measurable quantities
of total chromium at concentrations ranging between 1.01 to 6.94 µg/L. The 2L
value for total chromium is 10 µg/L.
Speciation analysis was conducted on ash pore water samples ABMW-01S and
ABMW-02S (Table 7-9). The concentration of hexavalent chromium Cr(VI) in
ash pore water samples ABMW-01S (0.025 µg/L) and ABMW-02S (0.026 µg/L)
were less than the EPA screening level for hexavalent chromium in residential
tap water (0.035 µg/L; USEPA Generic Screening Tables, June 26, 2015).
Consequently, there is no evidence to date that suggests that the concentration of
hexavalent chromium in coal ash pore water is greater than the EPA screening
value for tap water. However, speciation analysis was conducted on 17 samples
collected from 17 surficial aquifer downgradient groundwater monitor wells
(Table 10-3). The concentration of hexavalent chromium Cr(VI) exceeded the
EPA screening level for hexavalent chromium in residential tap water (0.035
µg/L; USEPA Generic Screening Tables, June 26, 2015) in samples collected from
the following wells:
Well ID Cr(VI) Concentration
AW-09B 0.038 µg/L
AW-09C 0.046 µg/L
MW-23B 0.051 µg/L
Consequently, hexavalent chromium is a surficial aquifer COPC; however,
hexavalent chromium is not a coal ash COPC. Therefore, hexavalent chromium
is not a surficial aquifer COPC potentially attributable to coal ash.
Iron is a COPC for coal ash pore water as well as surficial aquifer background
and downgradient groundwater. Iron was detected in one coal ash pore water
well (ABMW-02S; FADA) and in two surficial aquifer background wells (MW-
37B, MW-37C) at average concentrations of 25,333 µg/L and 4,950 µg/L,
respectively. Iron was detected in 97 out of 104 surficial aquifer groundwater
samples with 62 of the 97 detections at concentrations above the 2L (300 µg/L).
The average concentration of iron in samples that exceeded the 2L is 5,559 µg/L.
Confirmation sampling and statistical analyses may be required to determine if
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iron leaching from the coal ash is influencing iron concentrations in the surficial
aquifer.
Manganese, a coal ash pore water COPC, was detected in surficial aquifer
background and downgradient groundwater. Manganese was detected above
the 2L (50 µg/L) in every coal ash pore water sample and in 5 out of 7 surficial
aquifer background groundwater samples with maximum concentrations of 970
µg/L and 535 µg/L, respectively. Manganese was detected above the 2L in 68 out
of 104 surficial aquifer downgradient groundwater samples with maximum
concentrations of 2,120 µg/L in the AW-03B. Other surficial aquifer
downgradient wells having at least one groundwater sample containing
manganese concentrations greater than 1,000 µg/L are AW-04C (2,120 µg/L),
MW-24C (1,470 µg/L), and MW-31C (1,840 µg/L). Confirmation sampling and
statistical analysis may be required to determine whether manganese from coal
ash has impacted manganese concentrations in the surficial aquifer.
TDS concentrations exceeded the 2L (500 mg/L) in ash pore water well ABMW-
01S (760 µg/L April and 680 µg/L June, 2015) whereas TDS concentrations in
groundwater samples collected from surficial aquifer background wells did not
exceed 81 µg/L. TDS concentrations exceeded the 2L in 5 surficial aquifer
downgradient groundwater samples collected from 3 wells. The only surficial
aquifer downgradient well where TDS concentrations consistently exceeded the
2L is MW-31C where concentrations in three groundwater samples ranged
between 510 - 540 µg/L. The maximum TDS concentration was detected in well
AW-01B (910 µg/L February); however, the June groundwater sample (44 µg/L)
collected from well AW-01B did not confirm TDS concentrations above the 2L.
Confirmation sampling and statistical analyses may be required to confirm
elevated concentrations of TDS at these wells.
Vanadium was detected at concentrations above the IMAC (0.3 µg/L) in every
coal ash pore water sample (3.58 µg/L average; 8.72 µg/L maximum) whereas
vanadium was detected above the IMAC in 2 out of 4 surficial aquifer
background groundwater samples (1.15 µg/L average; 1.22 µg/L maximum) and
in 33 out of 73 surficial aquifer downgradient groundwater samples (2.04 µg/L
average; 39.6 µg/L maximum). This maximum vanadium concentration was
detected in a groundwater sample collected from well MW-20 which is located
between the FADA, former coal storage area, and the cooling water canal.
Confirmation sampling and statistical analysis may be warranted to determine
whether vanadium TDS in the surficial aquifer is naturally occurring or from an
on-site source.
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Sampling locations in the upper surficial and lower surficial aquifer where
constituent concentrations were greater than their screening criteria are
identified in Figures 12-3 and 12-4, respectively.
Downgradient Groundwater – Pee Dee Formation
Analytical results of Pee Dee Formation downgradient groundwater samples
collected in 2015 are presented in Table 12-5. The following constituents were
detected at concentrations above their respective 2L or IMAC or do not have a
groundwater screening value protective of human health:
Pee Dee Formation COPC
Potentially Attributable To Coal Ash Not A Coal Ash COPC(1)
Aluminum
Boron
Iron
Manganese
TDS
Vanadium
Antimony
Chloride
Total Chromium
Cobalt
Note (1): See Table 12-2
Antimony and total chromium detected in Pee Dee downgradient groundwater
samples above the IMAC (1 µg/L) and 2L (10 µg/L), respectively. Similarly,
chloride and cobalt were detected in multiple Pee Dee groundwater samples at
concentrations above the 2L (250 mg/L) or IMAC (1 µg/L), respectively.
However, antimony, total chromium, chloride, and cobalt are not coal ash
COPCs (Table 12-2). Consequently, antimony, total chromium, chloride, and
cobalt are not Pee Dee COPCs potentially attributable to coal ash.
Speciation analysis was conducted on ash pore water samples ABMW-01S and
ABMW-02S (Table 7-9). The concentration of hexavalent chromium Cr(VI) in
ash pore water samples ABMW-01S (0.025 µg/L) and ABMW-02S (0.026 µg/L)
was less than the EPA screening level for hexavalent chromium in residential tap
water (0.035 µg/L; USEPA Generic Screening Tables, June 26, 2015).
Consequently, there is no evidence to date that suggests that the concentration of
hexavalent chromium in coal ash pore water is greater than the EPA screening
value for tap water. However, speciation analysis was conducted on 9 samples
collected from 9 Pee Dee downgradient groundwater monitor wells (Table 10-3).
The concentration of hexavalent chromium Cr(VI) exceeded its EPA screening
level for hexavalent chromium in residential tap water (0.035 µg/L; USEPA
Generic Screening Tables, June 26, 2015) in samples from the following wells:
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Well ID Cr(VI) Concentration
AW-06E 0.064 µg/L
MW-23E 0.046 µg/L
Consequently, hexavalent chromium is a Pee Dee Formation COPC; however,
hexavalent chromium is not a coal ash COPC. Therefore, hexavalent chromium
is not a Pee Dee COPC potentially attributable to coal ash.
Aluminum is a coal ash COPC because it is in coal ash at concentrations greater
than soil RSL (Table 7-3) but does not have a 2L or IMAC. Aluminum was
detected in 20 out of 24 downgradient Pee Dee groundwater samples at
concentrations ranging from <5 µg/L to 96 µg/L. Aluminum may be eliminated
as Pee Dee COPC if it can be demonstrated that it is naturally occurring or a site-
specific groundwater criteria protective of human health is developed for
aluminum. Until then, aluminum is a Pee Dee COPC potentially attributable to
coal ash.
Boron was detected in every (24 out of 24) Pee Dee Formation groundwater
samples collected in 2015. Boron concentrations exceeded the 2L (700 µg/L) in 11
out of the 24 upper and lower Pee Dee Formation groundwater samples with the
average and maximum concentrations being 876 µg/L and 2,500 µg/L (MW-23E),
respectively. The presence of boron in the Pee Dee Formation may be attributed
to salt water intrusion (Sections 10.4 and 10.5); however, boron is a coal ash
COPC (Table 12-2) and will therefore be retained as a Pee Dee COPC potentially
attributable to coal ash.
Iron is a coal ash COPC and was detected in all Pee Dee groundwater samples at
concentrations ranging between 48 µg/L to 1,270 µg/L. Iron concentrations in 7
out of 24 Pee Dee samples were greater than 2L (300 µg/L). Consequently, iron is
a Pee Dee COPC potentially attributable to coal ash.
Manganese is a coal ash COPC and was detected in all Pee Dee groundwater
samples at concentrations ranging between 5 µg/L to 940 µg/L. Manganese
concentrations in 7 out of 24 Pee Dee samples were greater than the 2L (50 µg/L).
Consequently, manganese is a Pee Dee COPC potentially attributable to coal ash.
TDS is a coal ash COPC and was detected in all Pee Dee groundwater samples at
concentrations ranging between 320 mg/L to 1,500 mg/L. TDS concentrations in
14 out of 24 Pee Dee samples were greater than the 2L (500 µg/L). Consequently,
TDS is a Pee Dee COPC potentially attributable to coal ash.
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Vanadium is a coal ash COPC and was detected in 17 out of 24 Pee Dee
groundwater samples at concentrations ranging between <0.3 µg/L to 940 µg/L.
Vanadium concentrations in 7 out of 24 Pee Dee samples where greater than
IMAC (0.3 µg/L). Consequently, vanadium is a Pee Dee COPC potentially
attributable to coal ash.
COPCs potentially attributable to coal ash that have been retained for the Pee
Dee Formation are presented in Table 12-5. Figures 12-5 and 12-6 show sample
locations where these COPCs have been identified. Additional refinement of
COPCs for site-specific considerations will be included as part of a corrective
action plan.
Soils and Sediments
Soil samples were evaluated separately from sediments in order to appropriately
evaluate risk exposure scenarios for potential human receptors. Soils and
sediment analytical results were evaluated relative to USEPA soil Regional
Screening Levels (RSLs) protective of human health under residential-use and
industrial-use scenarios (USEPA Regional Screening Levels (RSLs) rev., June 26,
2015). The following constituents are not soil or sediment COPCs potentially
attributable to coal ash because they are not coal ash COPCs (Table 12-2):
Antimony
Beryllium
Cadmium
Calcium
Chloride
Total Chromium
Copper
Lead
Magnesium
Mercury
Molybdenum
Nickel
Nitrate (as N)
Potassium
Selenium
Sodium
Strontium
Sulfate
Thallium
Zinc
In addition, hexavalent chromium was detected in ash pore water samples
ABMW-01S (0.025 µg/L) and ABMW-02S (0.26 µg/L) at concentrations below the
EPA screening level (0.035 µg/L) for tap water (USEPA Regional Screening Levels
(RSLs) rev., June 26, 2015). Consequently, these constituents are not considered
soil or sediment COPCs attributable to coal ash and therefore, will not be
evaluated further.
Inorganic constituents that are coal ash COPCs but have no USEPA RSL values
protective of human health for soil are retained as a COPC potentially
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attributable to coal ash. These constituents will be retained as COPC potentially
attributable to coal ash until it can be demonstrated that constituent
concentrations are naturally occurring or a site-specific criteria protective of
human health is developed for inorganic constituents that have no soil RSLs
protective of human health.
Soil and sediment samples are often diluted by the analytical laboratory because
the concentrations of some target inorganic constituents (e.g., iron and
manganese) are beyond the range of their instrumentation. A consequence of
sample dilution is an increase in the analytical method detection limit of
constituents that may be present at much lower concentrations. If the analytical
method detection limit of a constituent is increased to a concentration that is
higher than its screening level, the constituent will be retained as a COPC
because it is possible that the constituent concentration may be greater than the
screening criteria but less than the elevated analytical method detection limit.
The constituent will retain the COPC designation unless it can be demonstrated
that its concentration is below the screening criteria. Prior to future sampling
events, the analytical laboratory will be provided with the screening criteria for
constituents that are retained as COPCs because their analytical method
detection limit was greater than their respective risk screening level. The
analytical laboratory will be asked to reanalyze samples at lower dilutions when
the analytical method detection limits of critical constituents are greater than
their respective risk screening level.
Soils
Surface soil samples were collected from the top two feet of soil borings installed
at the Site. Figure 2-1 identifies soil boring locations. Soil sample analytical
results are summarized in Table 12-6 and compared relative to USEPA soil
industrial-use and residential-use RSLs, as applicable.
No constituents were detected above their respective RSL in any of the 14
surficial soil (0 – 2 ft.) samples collected (Table 12-6); however, the analytical
method detection limits of antimony, cobalt and thallium were greater than some
or all of their respective soil industrial-use and/or residential-use RSLs.
Regardless, antimony, cobalt and thallium are not retained as COPCs potentially
attributable to coal ash because they are not coal ash COPCs (Table 12-2).
Arsenic was not detected in any of the 14 soil samples. However, the analytical
method detection limit for arsenic in six soil samples was greater than the soil
industrial-use RSL (3 µg/L) and the soil residential-use RSL (0.68 µg/L). Since
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arsenic is a coal ash COPC and it is not certain that arsenic concentrations in six
soil samples are below the soil industrial-use and residential-use RSLs, arsenic
will be retained as a soil COPC potentially attributable to coal ash. Arsenic may
be eliminated as a soil COPC potentially attributable to coal ash when
supplemental surficial soil sampling is conducted and arsenic concentrations or
their analytical method detection limits are below the soil residential RSL (0.68
µg/L).
The locations of surficial soil COPCs potentially attributable to coal ash are
presented on Figure 12-7.
Sediments
Sediment samples consist of samples collected at co-located surface water sample
locations identified on Figure 2-1. Following is a description of the locations
where sediment samples were collected:
Water
Body
Sediment and
Surface Water
Sample ID Sample Location Description
Lake
Sutton
SW-01C South end of Lake Sutton where cooling
channel begins
SW-004 East side of Lake Sutton adjacent to coal ash
management area and NPDES Outfall SW-004
SW-06A North end of Lake Sutton where cooling
channel ends and Lake Sutton begins
SW-08A Southwest on Lake Sutton
Cape
Fear
River
SW-CFUP Upstream relative to Lake Sutton
SW-CFP West of Lake Sutton
SW-CF001 Downstream relative to Lake Sutton
Evaluation of inorganic COPCs in sediments is based upon USEPA RSLs for soil
protective of human health under residential and industrial use scenarios.
Constituents that are coal ash COPCs and are detected in sediment samples at
concentrations that are greater than their respective industrial and/or residential-
use RSL, or their analytical method detection limits are greater than their
respective industrial and/or residential-use RSL are considered COPCs
potentially attributable to coal ash. In addition, inorganic constituents that are
coal ash COPCs and have no USEPA RSL for soil will be retained as a sediment
COPC potentially attributable to coal ash.
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Aluminum, barium, boron and vanadium are coal ash COPCs (Table 12-2);
however, all of these constituents were detected at concentrations below their
respective residential-use and industrial-use RSLs (Table 12-7). Consequently,
aluminum, barium, boron and vanadium are not sediment COPCs potentially
attributable to coal ash (Table 12-9).
Cobalt was detected in sediment sample SW-CFP (7.6 J mg/kg) at a concentration
that was greater than the residential-use RSL (2.3 mg/kg). In addition, the
analytical method detection limits for all other sediment samples are also greater
than the residential-use RSL (Table 12-7); however, cobalt is not a coal ash COPC
(Table 12-2). Therefore, cobalt is not a sediment COPC potentially attributable to
coal ash (Table 12-9).
Arsenic, a coal ash COPC (Table 12-2), was detected in sediment sample SW-06A
(4.6 J mg/kg) at an estimated concentration that was slightly more than the
industrial-use RSL (3 mg/kg) but was significantly greater than the residential-
use RSL (0.68 mg/kg). In addition, the analytical method detection limits for
arsenic in all other sediment samples were higher than the residential-use and
industrial-use RSLs (Table 12-7). Arsenic is a sediment COPC potentially
attributable to coal ash (Table 12-9).
Iron and manganese are coal ash COPCs (Table 12-2). They are also sediment
COPCs potentially attributable to coal ash because they were both detected at
concentrations above their respective residential-use RSLs in Cape Fear River
sediment samples SW-CF001 and SW-CFP (Table 12-9). Iron and manganese
were detected at concentrations below their respective RSLs in all other sediment
samples (Table 12-7).
The locations of sediment COPCs potentially attributable to coal ash are
presented on Figure 12-8.
Surface Water
Surface water analytical results were evaluated against the North Carolina
surface water standards (Subchapter 2B) and USEPA National Recommended
Water Quality Criteria (WQC) protective of human consumption of water and
organisms (NCDENR 4/22/15; USEPA 2015). Surface water sample locations are
shown on Figure 2-1. The locations of surface water COPCs potentially
attributable to coal ash are presented on Figure 12-9. Surface water analytical
results are summarized in Table 12-8 where they are compared to their
respective 2B concentrations and the EPA National Recommended WQC
protective of human health for the consumption of water and organisms (fish).
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A general description of the locations where surface water samples were
collected is presented in the previous section where sediment analytical results
are evaluated.
Aluminum and thallium were the only constituents detected at concentrations
greater than respective USEPA National Recommended WQC protective of
human consumption of water and organisms. Surface water 2B concentrations
for the protection of human health have not been established for aluminum or
thallium (Table 12-8).
Aluminum is a coal ash COPC (Table 12-2) and is a surface water COPC
potentially attributable to coal ash because the aluminum concentrations in all
nine surface water samples were greater than the USEPA National
Recommended WQC protective of human consumption of water and organisms
(6.5 µg/L). Aluminum concentrations ranged from 34 µg/L to 977 µg/L.
Although thallium was detected in surface water samples SW-004 (0.29 µg/L)
and SW-06A (0.249 µg/L) at concentrations slightly greater than the USEPA
National Recommended WQC protective of human consumption of water and
organisms (0.24 µg/L), thallium is not a surface water COPC potentially
attributable to coal ash because it is not a coal ash COPC (Table 12-2).
Boron, iron and manganese are coal ash COPCs and all were detected in five or
more of the nine surface water samples. Total and dissolved boron was detected
in five surface water samples at concentrations ranging from 185 µg/L to 211
µg/L. Total iron and total manganese were detected in every surface water
sample. Total iron concentrations ranged between 49 µg/L and 1,830 µg/L and
total manganese concentrations ranged between 8 µg/L and 121 µg/L. Surface
water 2B concentrations for the protection of human health and USEPA National
Recommended WQC protective of human consumption of water and organisms
have not been established for boron, iron, and manganese (Table 12-8).
Consequently, boron, iron and manganese will be retained as a surface water
COPC potentially attributable to coal ash until site-specific surface water criteria
protective of human health are developed for these compounds.
Summary
Table 12-9 summarizes human health risk assessment screening level COPCs
potentially attributable for each media that are.
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Site Specific Risk Based Remediation Standards 12.1.4
Based on the results of the preliminary comparison to risk-based screening
levels, media-specific remediation standards may be warranted in accordance
with the Eligibility Requirements and Procedures for Risk-Based Remediation of
Industrial Sites Pursuant to NC General Statutes 130A-310.65 to 310.77 as part of
a corrective action plan. If warranted, these standards will be calculated per the
corrective action plan based on the COPCs defined by the screening level risk
assessment.
12.2 Ecological Screening
Introduction 12.2.1
This screening level ecological risk assessment (SLERA) has been prepared in
accordance with the guidelines for conducting a SLERA for sites under the
authority of NCDENR Division of Waste Management. The objective of the
SLERA is to evaluate the likelihood that adverse ecological effects may result
from exposure to environmental stressors associated with conditions at the site.
This scope of work is equivalent to Step 1 - preliminary problem formulation and
ecological effects evaluation (USEPA, 1998) and Step 2 – estimation of the level of
a constituent exposure to a plant or animal at the site and comparison of the
maximum constituent concentrations to Ecological Screening Values.
Ecological Setting 12.2.2
12.2.2.1 Facility Site Summary
The Site is a former coal-fired electricity-generating facility located at 801
Sutton Steam Plant Road, Wilmington, New Hanover County, North
Carolina. The location of the Site is shown on Figure 1-1; the approximate
coordinates of the site are: latitude N 34.283296; longitude W -77.985860.
The Site utilizes an approximate 1100-acre cooling pond (i.e. Lake Sutton)
located adjacent to the Site and bounded by the Cape Fear River to the
west and ash basins (partially) to the east. There are three ash
management areas: (1) the Former Ash Disposal Area is bordered by the
plant, Lake Sutton, and the canal north of the plant; (2) the Old Ash Basin
Area is north of the same canal and east of Lake Sutton; (3) the New Ash
Basin Area is north of the Old Ash Basin Area and east of Lake Sutton.
12.2.2.2 Regional Ecological Setting
The Site is located in the Mid-Atlantic Floodplains and Low Terraces
ecoregion of North Carolina, a continuation of the Southeastern
Floodplains and Low Terraces ecoregion (Griffith et al. 2002).
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12.2.2.3 Description of Ecoregion and Expected Habitats
This region is characterized by hardwood forests often dominated by oak,
green ash, red maple, and hickories, and may contain some deepwater
Cypress-gum swamp areas (Griffith et al. 2002). This region also typically
includes large, slow rivers with swamps, ponds, oxbow lakes, and alluvial
deposits.
12.2.2.4 Watershed in which the Site is Located
The Cape Fear River watershed (that falls within six 8-digit catalog units),
is the state’s largest, encompassing approximately 9,300 square miles in all
or part of 26 counties (NCDENR).
12.2.2.5 Average Rainfall
Total annual precipitation in this region is approximately 49 inches
(http://www.usclimatedata.com/).
12.2.2.6 Average Temperature
The annual average high temperature is 74°F and the annual average low
temperature is 54°F (http://www.usclimatedata.com/).
12.2.2.7 Length of Growing Season
The growing season in Wilmington, NC is approximately 210 to 242 days
(based on two stations) (NCSU 2015).
12.2.2.8 Threatened and Endangered Species that use
Habitats in the Ecoregion
A list of state and federally threatened and endangered species for New
Hanover County is provided in Table 12-10.
12.2.2.9 Site-Specific Ecological Setting
A Checklist for Ecological Assessments/Sampling has been completed for
this site, and is provided (Appendix I).
12.2.2.10 On-site and Off-site Land Use
The Site was commissioned in 1954; this facility included three coal-fired
steam units and three combustion turbine units. The coal-fired units were
retired in November 2013 while the simple cycle combustion turbines
remain in operation. A new gas-fired, combined-cycle 625 megawatt
station began operation in November 2013, after the coal-fired units were
retired.
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The approximate size of the property is 3,300 acres, and consists primarily
of the former coal-fired unit structures, combined-cycle combustion units,
various other metal buildings, ash management areas, and a 1,100 acre
cooling pond (i.e. Lake Sutton). There is a 137 acre area with two ash
basins (e.g. Old Ash Basin Area, and New Ash Basin Area) containing
6,320,000 tons of ash. There is also an area called the “Former Ash
Disposal Area” that contains 840,000 tons of ash. The Cape Fear River
borders the Site on the west, approaching the Site north of Lake Sutton,
flowing south along the west side of the lake, turning east toward the Site
(i.e. south of the lake) and then meandering southward away from the
Site. The areas adjacent to the Cape Fear River consist mostly of
forested/shrub wetlands
(http://www.fws.gov/wetlands/data/mapper.HTML).
Existing ecological studies publically available for the site were reviewed.
In 2014, a wetland delineation of the Site was conducted by AMEC Foster
Wheeler, Inc. (AMEC) (Appendix I). The delineation identified 15
wetland areas and two jurisdictional tributary segments based on current
wetland and stream criteria established by the United States Army Corps
of Engineers (USACE) and North Carolina Division of Water Resources
(DWR).
12.2.2.11 Habitats within the Site Boundary
There are several potential habitats on the Site, including: mixed
pine/hardwood forest, wetlands, lake, and river areas. For a detailed
description of habitats, see the Checklist for Ecological
Assessments/Sampling in Appendix I.
12.2.2.12 Description of Man-made Units that May Act as
Habitat
The 1,100 acre Lake Sutton may act as a man-made aquatic habitat.
12.2.2.13 Site Layout and Topography
A general site layout can be found in Figure 1-2, and the topography is
consistent with the typical parameters of the Southeastern Plains
Ecoregion (e.g. relatively flat with areas of moderate to steep terraces
leading down to the Cape Fear River.
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12.2.2.14 Surface Water Runoff Pathways
The site has been graded in such as manner as to manage/divert runoff
(e.g. stormwater) using features such as swales, ditches, and culverts into
nearby water bodies (e.g. Cape Fear River, Lake Sutton).
12.2.2.15 Soil Types
The Southeastern Plains Ecoregion is generally composed of alluvium and
deposits of sand, silt, and gravel (Griffith et al. 2002). For a detailed
description of site lithology, see Section 6.1.1 of this report.
12.2.2.16 Species Normally Expected to Use Site under
Relatively Unaffected Conditions
Wildlife expected to be in the area of the site would potentially include
those listed in Table 12-10, and also other game and non-game wildlife
endemic to the Mid-Atlantic Floodplains and Low Terraces ecoregion of
North Carolina.
12.2.2.17 Species of Special Concern
The Cape Fear River Basin supports over 95 species of commercial and
recreational fish, including 42 rare aquatic species. The Cape Fear shiner
(Notropis mekistocholas), a federally endangered fish species, is known only
to inhabit this river. The shortnose sturgeon (Acipenser brevirostrum), red-
cockaded woodpecker (Leuconotopicus borealis), Saint Francis’ satyr
(Neonympha mitchellii francisci), and the West Indian manatee (Trichechus
manatus) (in estuarine areas) are also known species in the Cape Fear
River and are federally listed as endangered. The American alligator
(Alligator mississippiensis) and the loggerhead turtle (Caretta caretta) are
federally listed as threatened. See Table 12-10 for a full list of Threatened
and Endangered Species.
12.2.2.18 Nearby Critical and/or Sensitive Habitats
There are 15 wetland areas on-site that are identified in the 2014 wetland
delineation and depicted in the USFWS National Wetland Inventory. For
a detailed description, see the Checklist for Ecological
Assessments/Sampling (Appendix I).
Fate and Transport Mechanisms 12.2.3
Fate and transport mechanisms at this Site would include: erosion, storm water
runoff, and flow of surface water bodies.
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Conceptual Exposure Model
Consistent with standard risk assessment practice for developing conceptual
models, separate Conceptual Exposure Models (CEMs) were developed for the
human health and ecological risk evaluations. Figure 12-10 has been prepared
illustrating potential exposure pathways from the source area to possible
ecological receptors. The information in the CEM has been used in conjunction
with the analytical data collected as part of the CSA.
The ecological CEM is based on characterization of primary and secondary
sources and corresponding release mechanism sources, the COPC for each
affected environmental medium, and the migration and transport potential of
this constituent to potentially exposed populations (receptors). Figure 12-10
identifies the source and release mechanisms for the Site along with exposure
medium and route. Potential receptors at the Site are identified, with
consideration of current and future potential land use scenarios. The individual
components of the ecological CEM are further described in the following
sections.
Primary Constituent Source
The primary known source of site related constituents in groundwater at the Site
is from historical activities conducted in the ash basin. The affected soil, surface
water, and sediment in the vicinity of the ash pond serve as a secondary source.
Release and Transport Mechanisms
The potential constituent release and transport pathway at the Site are as follows:
Infiltration to groundwater.
Secondary Release Mechanisms
The secondary potential constituent release and transport pathways at the Site
are as follows:
Storm water runoff
Infiltration/percolation.
Exposure Medium, Pathways, and Exposure Routes
The exposure medium includes potentially impacted soil, surface water and
sediments at the site. Groundwater does not present a complete exposure
pathway to ecological receptors.
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The exposure routes associated with the potentially completed exposure
pathways evaluated for the Site include incidental ingestion and ingestion of
prey or plants.
Completed exposure pathways are the means by which potential receptors come
into contact with site-related COPCs. The completed exposure pathways under
current and future land use scenarios are identified in Figure 12-10 and include:
Terrestrial mammals
Aquatic mammals
Birds (including
waterfowl)
Benthic invertebrates
Herptiles
Fish
Insects
Aquatic vegetation
Algae/moss
Woody plants
Herbaceous plants
Preliminary Exposure Estimate and Risk Calculation 12.2.4
Exposure estimates used in the screening level ecological risk assessment are
represented by maximum concentrations of analytes detected in surface water,
seep, sediment, and soil samples. Hazard quotients (HQs) are defined as the
ratio of exposure estimates to ecological screening values (i.e. HQ = maximum
observed analyte concentration: ecological screening value). If exposure
estimates exceeded an ecological screening value (i.e. HQ>1), analytes were
retained as a COPCs for further consideration. COPCs are identified in the next
section.
Comparison to Ecological Screening Levels 12.2.5
A comparison of constituent concentrations in various media to the following
risk-based screening levels has been made and is presented in Tables 12-11 to 12-
13. These include species-specific screening levels based on constituent
concentrations that are Applicable or Relevant and Appropriate Requirements
(ARARs), designed for protection of ecological receptors from specific exposure
conditions that elicit toxic responses. These screening levels are derived from
risk-based calculations that set concentration limits using USEPA and state
standards for the following media:
Groundwater - Not applicable, as groundwater has no direct pathway to
ecological receptors
Surface water – 2B Criteria for Aquatic Life (NCDENR 2015a) and/or
USEPA National Recommended Water Quality Criteria for Aquatic Life
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(USEPA 2009) and/or USEPA Region 4 Surface Water Quality Criteria –
Chronic (USEPA 2001)
Soil - USEPA Region 4 Recommended Ecological Screening Values for
Soil (USEPA 2015b)
Sediment – USEPA Region 4 Recommended Ecological Screening Values
for Soil (USEPA 2015b) and/or USEPA Region 4 Effects Value – Sediment
(USEPA 2001)
Soil, sediment and groundwater background sample data from prior
investigations are considered, as well as regional and national background data,
as available
Groundwater
Direct exposure pathways of groundwater to ecological receptors are incomplete,
and therefore do not pose any appreciable risk.
Surface Water
Surface water samples were evaluated in order to appropriately evaluate risk
exposure scenarios for potential ecological receptors. Surface water samples
consist of samples collected from the water column (i.e. below the water/air
interface when feasible) at selected sample locations. Figure 1-2 shows the
locations of the surface water sample locations at the Site.
As detailed Tables 12-11 and 12-14, the following inorganic constituents are
excluded from the list of ecological COPCs for surface water because either (a)
maximum detected concentrations were less than comparison criteria, or (b) the
constituents were not detected in the sample and their detection limit values
were less than all comparison criteria (2B Criteria for Aquatic Life and/or USEPA
National Recommended Water Quality Criteria for Aquatic Life and/or USEPA
Region 4 Surface Water Quality Criteria – Chronic):
Antimony
Arsenic
Boron
Chloride
Chromium
Iron
Mercury
Nickel
Selenium
Thallium
The following inorganic constituents will be retained as COPCs for further
evaluation because their maximum detected concentrations were greater than
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comparison criteria (2B Criteria for Aquatic Life and/or USEPA National
Recommended Water Quality Criteria for Aquatic Life and/or USEPA Region 4
Surface Water Quality Criteria – Chronic):
Aluminum
Copper
Zinc
Total aluminum was detected in six surface water samples at concentrations
greater than USEPA National Recommended Water Quality Criteria for Aquatic
Life – Chronic (87 µg/L) and USEPA Region 4 Surface Water Quality Criteria –
Chronic (87 µg/L).
Dissolved copper was detected in five surface water samples at concentrations
greater than USEPA Region 4 Surface Water Quality Criteria – Chronic (0.00654
mg/L) and 15A NCAC 2B Criteria for Aquatic Life – Acute and Chronic (0.0036
mg/L and 0.0027 mg/L, respectively).
Dissolved zinc was detected in three surface water samples (SW-004, SW-06A,
and SW-CFUP DUP) at concentrations greater than all comparison criteria. The
result at SW-CFUP DUP may be anomalous, as total zinc in the same location ID
was measured at 0.0068 mg/L, which more closely mirrors the SW-CFUP sample
results (Table 12-11). Dissolved zinc was detected in one surface water sample
(SW-CFUP) at a concentration greater than USEPA Region 4 Surface Water
Quality Criteria – Chronic (0.00654 mg/L) and 15A NCAC 2B Criteria for Aquatic
Life – Acute and Chronic (0.0036 mg/L). Dissolved zinc was detected in three
surface water samples at concentrations greater than 15A NCAC 2B Criteria for
Aquatic Life – Acute and Chronic (0.0036 mg/L).
The following constituents will be added to the list of COPC uncertainties since
they are not subject to published 2B Criteria for Aquatic Life or USEPA National
Recommended Water Quality Criteria for Aquatic Life:
Barium
Cobalt
Manganese
Methane
Molybdenum
Nitrite/Nitrate
Strontium
Sulfate
Sulfide
Vanadium
Calcium, magnesium, potassium, and sodium are omitted from the list of COPCs
as they have no applicable criteria, are ubiquitous in nature, and are considered
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to be macrominerals with negligible toxicity to ecological receptors. These
constituents were quantified as a component of the water characterization
process.
Soil
Soil samples were evaluated separately from sediments in order to appropriately
evaluate risk exposure scenarios for potential ecological receptors. Surface soil
samples were collected from the top two feet of soil borings conducted at the Site
facility. Figure 1-2 shows the locations of the soil borings.
The following inorganic constituents (Tables 12-12 and 12-14) are excluded from
the list of ecological COPCs for surface soils because their maximum detected
concentrations were less than their respective comparison criteria for soils, or (b)
the constituents were not detected in the sample and their detection limit values
were less than all comparison criteria (USEPA Region 4 Recommended
Ecological Screening Values for Soil):
Arsenic
Barium
Beryllium
Cadmium
Cobalt
Copper
Lead
Manganese
Mercury
Nickel
Zinc
The following constituents will be retained as COPCs for further evaluation
because their maximum detected concentrations in soil were greater than their
respective comparison criteria for soils (USEPA Region 4 Recommended
Ecological Screening Values for Soil):
Aluminum
Chromium
Iron
Vanadium
Aluminum was detected in ten of 14 samples at concentrations greater than
USEPA Region 4 Recommended Ecological Screening Values for Soil (50 mg/kg).
Chromium was detected in six of 14 samples at concentrations greater than
USEPA Region 4 Recommended Ecological Screening Values for Soil (0.4 mg/kg).
Iron was detected in eight of 14 soil samples at concentrations greater than
USEPA Region 4 Recommended Ecological Screening Values for Soil (200
mg/kg).
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Vanadium was detected in five of 14 samples at concentrations greater than
USEPA Region 4 Recommended Ecological Screening Values for Soil (2 mg/kg).
Antimony, boron, molybdenum, selenium, thallium, and vanadium will be
added to the list of COPC uncertainties due to lack of quantifiable analytical
results. Antimony had several results that were less than the detection limit,
which was greater than USEPA Region 4 Recommended Ecological Screening
Values for Soil (3.5 mg/kg).
Boron was detected at less than the detection limits in all samples, which were
greater than USEPA Region 4 Recommended Ecological Screening Values for
Soil (0.5 mg/kg).
Molybdenum had four results less than detection limit values, which were
greater than USEPA Region 4 Recommended Ecological Screening Values for
Soil (2 mg/kg).
Selenium was detected at less than the detection limits in all samples, which
were greater than USEPA Region 4 Recommended Ecological Screening Values
for Soil (0.81 mg/kg).
Thallium had ten results less than detection limit values, which were greater
than USEPA Region 4 Recommended Ecological Screening Values for Soil (1
mg/kg).
Vanadium, while having five instances of exceeding USEPA Region 4
Recommended Ecological Screening Values for Soil (2 mg/kg), also had six
instances of the detection limit being greater than this criterion.
The following constituents will be added to the list of COPC uncertainties since
they are not subject to published USEPA Region 4 Recommended Ecological
Screening Values for Soil:
Calcium
Nitrate
Strontium
Sulfate
Calcium, magnesium, potassium, and sodium are omitted from the list of COPCs
as they have no applicable criteria, are ubiquitous in nature, and are considered
to be macrominerals with negligible toxicity to ecological receptors. These
constituents were quantified as a component of the soil characterization process.
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Sediment
Sediment samples were collected at co-located surface water locations identified
on Figure 1-2. As summarized on Tables 12-13 and 12-14, the following
inorganic constituents are excluded from the list of ecological COPCs for
sediment because either (a) their maximum detected concentrations were less
than their respective comparison criteria (USEPA Region 4 Recommended
Ecological Screening Values for Soil and/or USEPA Region 4 Effects Values for
Sediment), or (b) the constituents were not detected in the sample and detection
limit values were less than both comparison criteria:
Barium
Beryllium
Cadmium
Cobalt
Copper
Lead
Mercury
Nickel
The following constituents will be retained as COPCs for further evaluation
because their maximum detected concentrations in soil were greater than their
respective comparison criteria for soils (USEPA Region 4 Recommended
Ecological Screening Values for Soil and/or USEPA Region 4 Effects Values for
Sediment):
Aluminum
Boron
Chromium
Iron
Manganese
Molybdenum
Vanadium
Zinc
Aluminum was detected in all sediment samples at concentrations exceeding the
USEPA Region 4 Recommended Ecological Screening Values for Soil (50 mg/kg).
Boron was detected in one sediment sample (SW-06A), which exceeded USEPA
Region 4 Recommended Ecological Screening Values for Soil (0.5 mg/kg). This
result, however, was below the reporting limit, and therefore estimated. The
remainder of samples had detection limits greater than this criterion.
Chromium was detected in all sediment samples at concentrations greater than
USEPA Region 4 Recommended Ecological Screening Values for Soil (0.4 mg/kg).
Iron was detected in all sediment samples at concentrations greater than USEPA
Region 4 Recommended Ecological Screening Values for Soil (200 mg/kg).
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Manganese was detected in four sediment samples at concentrations greater than
USEPA Region 4 Recommended Ecological Screening Values for Soil (100
mg/kg).
Molybdenum was detected in one sediment sample (SW-004) at a concentration
greater than USEPA Region 4 Recommended Ecological Screening Values for
Soil (2 mg/kg). Two other samples had detection limits greater than this
criterion.
Vanadium was detected in six sediment samples at concentrations greater than
USEPA Region 4 Recommended Ecological Screening Values for Soil (2 mg/kg).
The remaining sample had a detection limit greater than this criterion.
Zinc was detected in one sediment sample (SW-CFP) at a concentration greater
than USEPA Region 4 Recommended Ecological Screening Values for Soil (50
mg/kg).
Antimony, arsenic, boron, molybdenum, selenium, thallium, and vanadium will
be added to the list of COPC uncertainties due to lack of quantifiable detections.
Antimony was not detected in any samples, but detection limits for all sample
analyses were greater than USEPA Region 4 Recommended Ecological Screening
Values for Soil (3.5 mg/kg) and USEPA Region 4 Effects Values for Sediment (2
mg/kg).
Arsenic had detection limits greater than USEPA Region 4 Recommended
Ecological Screening Values for Soil (10 mg/kg) and EPA Region 4 Effects Values
for Sediment (7.24 mg/kg) in two analyses.
Boron had detection limits greater than USEPA Region 4 Recommended
Ecological Screening Values for Soil (0.5 mg/kg) in all but one analysis.
Molybdenum was not detected in three samples with detection limits greater
than USEPA Region 4 Recommended Ecological Screening Values for Soil (2
mg/kg).
Selenium was not detected in any samples, all of which had detection limits
greater than USEPA Region 4 Recommended Ecological Screening Values for
Soil (0.81 mg/kg).
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Thallium was not detected in any samples, but detection limits for all sample
analyses were greater than USEPA Region 4 Recommended Ecological Screening
Values for Soil (1 mg/kg).
Vanadium was not detected in one sample with a detection limit greater than
USEPA Region 4 Recommended Ecological Screening Values for Soil (2 mg/kg).
The following constituents will be retained as sediment uncertain COPCs for
further evaluation because they do not have a published USEPA Region 4
Recommended Ecological Screening Values for Soil:
Calcium
Nitrate
Strontium
Sulfate
Table 12-14 summarizes ecological COPCs retained for each medium. Figures
12-11 to 12-13 show sample locations with COPCs.
12.3 Uncertainty and Data Gaps
This screening level risk assessment was conducted as part of the groundwater
assessment under the primary assumption that sampling locations, sample media, and
analytes, as defined in the Work Plan, were sufficient for screening human health and
ecological risks at the Site. All proposed samples were collected, and analyses
completed as planned; however, due to analytical constraints (e.g., method detection
limits and dilution effects during sample preparation for analysis) and/or anomalous
results, there are numerous constituents for which (a) detection limits were greater than
one or more screening criteria, (b) reported results were greater than detection limits,
but less than reporting limits (i.e., estimated), or (c) reported results seemed anomalous
(e.g., dissolved metal concentration greater than total metal concentration). This
presents the possibility that the actual concentration of a given constituent might exceed
one or more screening criteria while not being detected by instrumentation, the result
was incorrectly estimated, or some unknown error occurred which interfered with
accurate reporting. For this reason, these particular instances have been noted and
affected constituents flagged as COIs that require further consideration. The COIs
flagged for these reasons include antimony, arsenic, beryllium, boron, cadmium, lead,
molybdenum, selenium, sulfide, thallium, and vanadium.
12.4 Scientific/Management Decision Point
Based on the results of the human health and ecological screen, media-specific
remediation standards will be calculated in accordance with the Eligibility
Requirements and Procedures for Risk-Based Remediation of Industrial Sites Pursuant
to NC General Statutes 130A-310.65 to 310.77 after additional sample collection.
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12.5 Risk Assessment Summary
The Screening Level Human Health and Ecological Risk Assessments conducted as part
of this groundwater assessment resulted in the identification of the following COPCs
(in groundwater, surface water, sediment, and/or soil) at the Site: pH, aluminum,
antimony, arsenic, barium, boron, chloride, chromium, cobalt, copper, iron, lead,
manganese, molybdenum, nitrate (as N), selenium, thallium, TDS, vanadium, and zinc
(Tables 12-9 and 12-14). Calcium, magnesium, potassium, and sodium are omitted
from the list of COPCs as they have no applicable criteria, are ubiquitous in nature, and
are considered to be macrominerals with negligible toxicity to ecological receptors.
These constituents were quantified as a component of the water, soil, and sediment
characterization processes. To summarize: the potential exists for exposure of the
COPCs listed above to human and/or ecological receptors, as identified in the CEMs
(Figures 12-1 and 12-10), at levels exceeding those listed in one or more screening
criteria.
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13.0 GROUNDWATER MODELING
A brief synopsis of the groundwater modeling effort is included in the following
sections.
13.1 Groundwater Modeling to be Performed in CAP
The proposed numerical modeling involves development of a groundwater flow model
and a chemical transport model. The groundwater modeling will be conducted in
accordance with the requirements of the May 31, 2007 NCDENR Memorandum titled
Groundwater Modeling Policy.
The numerical groundwater flow model will be developed using MODFLOW, a three-
dimensional finite difference groundwater model created by the United States
Geological Survey (USGS). In MODFLOW, Darcy’s law and the conservation of mass
are used to derive balance equations for each finite difference cell. MODFLOW
considers three-dimensional transient groundwater flow in confined and unconfined
heterogeneous systems, and it can included dynamic interaction with pumping wells,
recharge, evapotranspiration, rivers, streams, springs, lakes, and swamps.
The numerical model will be used as a quantitative conceptual model of the Site where
flow features such as boundary conditions, sources and sinks, material zones,
hydrologic parameters, and external stresses will be defined. The boundaries of the
flow model will be located far (several miles) away from the Site so that boundary
conditions do not dominate the modeled flow regime. The boundary conditions will
depend on the type of boundary, but will be either specified head (for surface water
boundaries), or no-flow (for groundwater divides). Parts of the boundary may be
modeled using a specified or head-dependent flux.
The Site model sources and sinks will consist of drains, springs, rivers, swamps and
ponds, industrial production wells and water supply wells. Material zones or
hydrostratigraphic layers will be defined from previously existing boring logs in
addition to the 52 boring logs generated during the 2015 assessment. Recharge,
evapotranspiration, and precipitation are representations of external stresses that are
used in the model. Recharge will be initially estimated using the average characteristics
of the regional hydrogeology. These initial estimates will then be refined during a
model calibration process where the model parameters are adjusted to provide a better
match with Site field data.
To further define heterogeneities, a 2-D scatter point set will be used to define specified
hydraulic values within vertical or horizontal zones. Specified hydraulic values will be
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given set ranges that reflect field conditions from core measurements, historical slug
and pump tests from Geosyntec (2012), and recent slug tests from the 42 wells installed
under the GAP. The model will be calibrated in part by adjusting the specified
hydraulic value distribution to minimize the residuals between the predicted hydraulic
heads and the observed values. Historical hydraulic heads and recent June 2015
measurements from 96 wells will be used as observed values.
The chemical transport model will use the Modular 3-D Transport Multi-Species model,
which uses the groundwater flow field from MODFLOW to simulate three-dimensional
advection and dispersion of the dissolved COCs including the effects of retardation due
to COC adsorption to the soil matrix. The COC source terms will consist of initial
distributions of the COCs in the subsurface that are estimated from Site boring and
observation well data. During the calibration process, these source terms, and to a
lesser extent some of the transport parameters will be adjusted to provide a best match
with the field COC data.
Model limitations will be primarily related to uncertainties in field data. Model
confidence will always be higher in areas where a high density of field data can
constrain the model. Numerical model errors are easily recognizable and minimized by
experienced users.
13.2 Description of Kd Term Development
An adaptation of the column method described by Daniels and Das (2014) to develop
Kd estimates was used on Site soil samples. Soil samples with measured dry density
and maximum particle size of 2 mm were placed in lab-scale columns configured to
operate in the up-flow mode. A solution with measured concentrations of the COI was
pumped through each column, effluent samples will be collected at regular intervals
over time.
When constituent breakthroughs are verified, a “clean” solution (no COIs) will be
pumped through the columns and effluent samples collected. Samples will be analyzed
by inductively coupled plasma-mass spectroscopy (ICP-MS) and ion chromatography
(IC). Plots of effluent COI concentration versus cumulative pore volumes exchanged
will be analyzed to estimate Kd values and to confirm reversibility of COI sorption. Kd
factors for boron, iron, manganese, and vanadium will be utilized in the transport
model.
13.3 Description of Flow Transects
Groundwater flow from the ash basins to potential receptor areas is to the east and
southeast (Figure 6-6 through 6-8). Three transects were selected for the Site to
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illustrate flowpath conditions in the vicinity of the ash basin (Figures 1-2). Section A-A’
(Figure 6-1) provides the best illustration of the three ash basin source areas in relation
to the undeveloped area to the north, the Site and receptor area to the east. Sections B-
B’ and C-C’ (Figure 6-2) illustrate conditions from the cooling pond eastward through
the 1971 ash basin area to the Site perimeter.
13.4 Other Model Inputs
At a Coastal Plain site such as Site, the stratigraphy of the sedimentary units in the
subsurface is the primary component of the model. Key components of the model
include the contact between the surficial aquifer and the Pee Dee Formation and the
characteristics of the lower surficial aquifer.
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14.0 DATA GAPS – SITE CONCEPTUAL MODEL UNCERTAINTIES
Information to date is sufficient to prepare a SCM and to support preparation of the
groundwater model for the Site. Although data gaps remain they are not a limiting
factor in developing the SCM or are anticipated to be a limiting factor for completion of
the groundwater modeling or development of the CAP.
The primary data gaps that have been identified during this assessment is the
determination of deep (Pee Dee Formation) background concentrations and the
determination of potential off-site sources of COIs.
14.1 Data Gaps
Data gaps identified during the assessment include the following:
Identification of the background levels of COIs in deep aquifer zones.
Insufficient groundwater analytical data to rule out the 1984 ash basin as a source
of selenium detected MW-27B.
Determination of off-site sources responsible for concentrations of COIs east and
northeast of the Site.
14.2 Site Heterogeneities
Sedimentary geologic units at the site include the surficial alluvial deposits underlain
by sediments of the Pee Dee Formation. Heterogeneities among these units are
discussed below.
The surficial deposits include an upper zone of relatively homogenous medium-fine
sand. The lower surficial contains more heterogeneity of grain size, including zones of
coarse sand to fine gravel, and in some cases large pieces of wood. Greater
groundwater flow, as evidenced by greater hydraulic conductivity values, is facilitated
through this zone.
The Pee Dee Formation underlies the surficial deposits unconformably across the Site.
Pee Dee sediments are made up of dense fine sands, often silty or clayey. The contact
between surficial deposits and the Pee Dee is sharp and distinct. Lateral groundwater
flow is enhanced by this heterogeneity.
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14.3 Impact of Data Gaps and Site Heterogeneities
Additional deep wells outside of the ash basin a can provide data on background levels
in the lower Pee Dee Formation. Additional monitoring of existing wells will assist in
determining if off-site conditions are impacting assessment wells. Pending
groundwater modeling and Kd analyses of soil retardation factors will also provide
additional data regarding the effects of the Site heterogeneities. These data gaps will
not compromise the groundwater modeling or the CAP.
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15.0 PLANNED SAMPLING FOR CSA SUPPLEMENT
The following sample collection is anticipated to supplement the CSA:
• Collection of groundwater sample from wells located north of 1984 ash basin
(PZ-1A/B and MW-36B/C) and/or installation of additional wells in this area for
the purpose of metals analyses.
• Speciation sampling of chromium for wells located along the eastern Site
boundary.
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16.0 INTERIM GROUNDWATER MONITORING PLAN
The outline for an interim groundwater monitoring plan is contained in this section.
16.1 Sampling Frequency
Groundwater samples would continue to be collected three times per year. The
schedule followed for the existing compliance sampling has yielded meaningful
seasonal data that can assist in the development of the SCM.
16.2 Constituent and Parameter List
The proposed list of constituents for analysis is included as Table 16-1.
16.3 Proposed Sampling Locations
Proposed groundwater monitor wells to be included in the interim groundwater
sampling program are listed in Table 16-2 and illustrated on Figure 16-1.
16.4 Proposed Background Wells
Of the monitor wells listed in Table 16-2, wells at locations MW-5B/C and MW-37B/C
would be designated background wells.
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17.0 DISCUSSION
All aspects of the GAP were accomplished, with the exception of the infiltration tests
that were superseded by in-situ hydraulic conductivity testing. The SCM for the Site
entails the following major components:
The ash basins and FADA sit atop Coastal Plain sediments north and northwest of the
main plant area.
Regional groundwater flow is generally south toward the convergence of the Cape Fear
and East Cape Fear River. At the Site, groundwater flow is somewhat complex and is
affected by topography, the ash basin and cooling pond as well as the operation of
nearby production and water supply wells. Groundwater flows in all directions from
the ash basin but the salient flow direction is to the east and southeast. The potential
interferences from the off-site municipal and industrial production wells (and the
potential extraction wells) will be considered in the groundwater flow model is being
prepared for the CAP. As the model is being prepared additional groundwater and
surface water elevation monitoring points may be collected.
Ash pore water in the FADA and 1971 ash basins infiltrate directly into the porous
surficial aquifer below. No seeps or surface drains direct ash pore water from the
basins.
The vertical migration of COIs has been reduced by the lower permeability of the Pee
Dee Formation. The COIs are most prevalent in the lower surficial aquifer.
Concentrations of COIs related to the ash basins, particularly boron, have migrated off-
site to the east. A Groundwater Mitigation and Monitoring Plan, which includes the
installation of 12 extraction wells screened in the lower surficial aquifer, has been
submitted to address this condition.
17.1 Maximum COI Concentrations
COI concentrations above 2L extend beyond the compliance boundary and beyond the
eastern Site boundary. The highest concentrations are generally found in the ash pore
water or wells near the ash management area. High levels of iron and manganese occur
in the northeast portion of the Site and in off-site wells which do not appear to be
connected to the Site ash management area.
Migration of COIs to surface water is indicated by comparison of well water level data
in the FADA and 1971 ash basins to the surface water level of the cooling pond.
However, no impact to the surface water is indicated based on laboratory data.
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17.2 Summary of Completed and Ongoing Work
Work anticipated under the GAP was completed.
17.3 Contaminant Migration and Potentially Affected Receptors
Potential receptors of COIs exist in off-site private and public water supply wells.
Concentrations of boron near 2L have been detected in two private wells.
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18.0 CONCLUSIONS AND RECOMMENDATIONS
The conclusions developed during the CSA are summarized in this section.
18.1 Source and Cause of Contamination
Coal ash accumulated in the ash basins and FADA are sources of groundwater impact.
The cause of impact is leaching of constituents from the coal ash into the ash pore water
and its migration to underlying groundwater
18.2 Imminent Hazards to Public Health and Safety and Actions
Taken to Mitigate Them
15A NCAC 02L .0106(g)(2) requires the site assessment to identify any imminent
hazards to public health and safety and the actions taken to mitigate them in accordance
with Paragraph (f) of .0106(g). Paragraph (f) provides requirements for corrective
action. Potential impact to water supply wells located to the east of the Site is being
addressed. Several steps that have been initiated include:
A Groundwater Mitigation and Monitoring Plan has been submitted that
includes the installation of 12 extraction wells along the eastern Site boundary to
intercept groundwater in the surficial aquifer.
Plans to discontinue the use of the nearby municipal water supply wells are
underway. Completion of the replacement well field water system construction
is anticipated by December 2015.
Preparations are being made to excavate the ash from the basins, thus removing
the source of groundwater impact.
18.3 Receptors and Significant Exposure Pathways
The requirement contained in the NORR and the CAMA concerning receptors was
completed with the results provided in Section 4. A screening level human health risk
assessment and screening level ecological risk assessment was performed with the
results provided in Section 12.
Consumption of groundwater, recreational use of affected surface water, and
consumption of fish and game affected by contaminants are the primary exposure
pathways for humans in the vicinity of the ash basin. Cape Fear Public Utility
Authority water supply wells are located adjacent to the Site on the east side. These
wells produce water from the surficial aquifer at a depth of approximately 50 feet bgs.
These well are located downgradient of the Site based on data collected in the CSA.
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Thirty-two private water wells were identified within 0.5 miles of the Site compliance
boundary during the CSA.
Public and private wells that are located near the eastern Site boundary have been
surveyed. NCDENR has managed the sampling of water supply wells in the area. No
COIs are detected above the 2L in the public supply wells with the exception of
manganese. Based on data obtained during the assessment, the occurrence of
manganese in the area of the public supply wells cannot be conclusively attributable to
the ash basins. In the private wells, only iron, manganese, cobalt, and vanadium were
reported at concentrations greater than 2L or IMAC. Based on data obtained during the
assessment, the occurrence of iron, manganese and cobalt in the wells cannot be directly
attributed to the ash basins. Vanadium is also a naturally-occurring element in
groundwater and assessment data does not definitively indicate a connection between
the detection of vanadium in the supply wells and the ash basins. Boron results for the
water supply wells sampled at the direction of NCDENR were reported to be less than
the 2L.
The installation of extraction wells and the replacement of the public well supply wells
are planned to close potential exposure pathways to these receptors.
18.4 Horizontal and Vertical Extent of Soil and Groundwater
Contamination
The horizontal extent of COIs in soil and groundwater has been delineated. No surficial
soil impact was detected with the exception of iron, which is representative of
background concentrations.
Groundwater impact is considered to be present where the analytical results were in
excess of the site background concentrations and in excess of the 2L or IMAC Standard.
Arsenic, barium, boron, iron, manganese, vanadium and total dissolved solids (TDS)
have been identified as site specific constituents of interest (COIs) based on
concentrations in excess of the 2L Standard or IMAC concentration in ash pore water.
Horizontal groundwater impact has been defined by monitor wells on-site to the north
and south and off-site to the east. Wells could not be installed west of the ash basins
due to the presence of the cooling pond and Cape Fear River, however, surface water
data and groundwater elevation data do not indicate the need for further assessment in
that direction.
Vertical delineation has been defined in the upper portion of the Pee Dee Formation,
assuming the chloride concentrations in the lower Pee Dee wells are indicative of salt
water intrusion and account for the boron concentrations detected at that level. This
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assumption is supported by several lines of evidence based on the data collected. The
screen elevations of the Pee Dee wells are approximately 80 to 130 feet below sea level
and the Site is located in close proximity to the Atlantic coast. Numerous pumping
wells are located in the vicinity of the Site which would help facilitate salt water
intrusion. The average chloride concentration in the Pee Dee wells is nearly eight times
that of the surficial wells and the specific conductance is nearly four times greater in the
Pee Dee wells than in the surficial wells. Additionally, regional groundwater data also
indicate naturally-occurring, elevated boron levels in sea water.
Constituent transport is dependent on leaching from the coal ash source that results
from solubility due to chemical disequilibrium (the dissolved phase is more stable than
the solid phase under the conditions at the time). Factors that affect reactions with
material along the flow path resulting in removal of the constituents from groundwater
control the extent of migration. These factors vary by constituent and vary based on the
properties of the soil or aquifer materials along the flow path.
Sorption and precipitation are the primary mechanisms that immobilize cations
(aluminum, arsenic, boron, cobalt, iron, manganese, thallium, and vanadium). A
number of factors specific to constituent and to the site conditions are involved in
determining which of these mechanisms occur and how much of the constituent is
partitioned out of the groundwater.
The results of testing performed to determine the chemical, physical, and mineralogical
characteristics of the soil and aquifer materials and the site groundwater were
performed during the CSA. Additional testing is being performed to determine the
adsorptive capacity of the site soils and aquifer materials to the specific groundwater
constituents by development of site specific partition coefficient Kd terms. The Kd
testing will provide site specific values for the ability and capacity of site soils to
remove constituents from groundwater and will assist in understanding the
mechanisms affecting transport at the site. Kd tests and the associated groundwater
modeling will also allow for evaluation of the long-term constituent loading and the
capacity of the site soil and aquifer material to attenuate this loading. The results of this
testing, the groundwater modeling, and the evaluation of the long term groundwater
conditions at the site will be presented in the CAP.
Iron, manganese, and vanadium are commonly detected in shallow groundwater in the
coastal plain region of North Carolina. Calculation of proposed site specific
background concentrations will occur when a sufficient number of samples to perform
statistical analysis have been collected.
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18.5 Geological and Hydrogeological Features influencing the
Movement, Chemical, and Physical Character of the
Contaminants
The primary feature that influences migration of contaminants is the permeable nature
of the surficial aquifer in contrast with the underlying Pee Dee Formation. While no
confining unit was discovered at the Site as anticipated in the initial site conceptual
model presented in the Work Plan dated December 30, 2014, data collected to date
indicate that vertical migration is slowed by the lower permeability of the Pee Dee
Formation approximately 50 feet bgs at the Site. The contrast in permeabilities between
the surficial unit and the underlying Pee Dee is sufficient to create preferential lateral
flow at the Site.
The movement of the contaminants is related to the groundwater flow direction, the
groundwater flow velocity, and the rate at which a particular contaminant reacts with
materials in the aquifer. The direction of the movement of the constituents confirmed
by the CSA is toward the east and south, as anticipated. The rate of groundwater
movement varies with the hydraulic conductivity and porosity of the site soil and rock
materials and ranges from 0.185 to 8.55 feet per year.
Data collected during the CSA, coupled with Kd data to be supplied at a later date, will
be used to build groundwater flow and transport models for the site. The groundwater
model will provide information to allow evaluation of the capacity of the site soil and
aquifer material to attenuate the loading imposed by the conditions modeled for the
proposed corrective action.
18.6 Proposed Continued Monitoring
Interim groundwater monitoring is proposed in Section 16.
18.7 Preliminary Evaluation of Corrective Action Alternatives
A Groundwater Mitigation and Monitoring Plan has been submitted that includes the
installation of 12 extraction wells along the eastern Site boundary to intercept elevated
levels of boron in groundwater from the surficial aquifer.
Groundwater modeling will provide an estimate of the degree of residual groundwater
impact over time. In the subsequent CAP, Duke Energy will pursue corrective action
under 15A NCAC 02L .0106 (k) or (l) depending on the results of the groundwater
modeling and the evaluation of site suitability for monitored natural attenuation.
Evaluation of monitored natural attenuation would be performed using the approach
found in Monitored Natural Attenuation of Inorganic Contaminants in Groundwater,
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Volumes 1 and 2 (EPA Reference) and potential modeling of interaction between
groundwater and surface water.
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19.0 REFERENCES
ASTM D6312-98: Standard Guide for Developing Appropriate Statistical Approaches
for Groundwater Detection Monitoring Programs. 2012.
ASTM E1689-95: Standard Guide for Developing Conceptual Site Models for
Contaminated Sites. 2014.
ASTM D4044-96: Standard Test Method (Field Procedure) for Instantaneous Change in
Head (Slug) Tests for Determining Hydraulic Properties of Aquifers.
Cox, J.A., Lundquist, G.L., Przyjazny, A., and Schmulbach, C.D. Leaching of Boron
from Coal Ash. Environmental Science and Technology. 1978: 722-723.
Daniel, C.C., III, and Sharpless, N.B. Ground-water supply potential and procedures for well-
site selection upper Cape Fear basin, Cape Fear basin study, 1981-1983. North Carolina
Department of Natural Resources and Community Development and U.S. Water
Resources Council in cooperation with U.S. Geological Survey. 1983: 73.
Daniels, John L. and Das, Gautam P. Practical Leachability and Sorption Considerations for
Ash Management. Boston, MA: Wentworth Institute of Technology Geo-Congress
2014 Technical Papers: Geo-characterization and Modeling for Sustainability.
2014.
Denbigh, K. The Principles of Chemical Equilibrium. 3rd ed. Cambridge, UK:
Cambridge University Press. 1971: 494.
Dudas, M.J. Long-Term Leachability of Selected Elements from Fly Ash. Environmental
Science and Technology. 1981: 840-843.
Duke Energy, http://www.duke-energy.com/pdfs/duke-energy-ash-metrics.pdf
(Updated Oct. 31, 2014)
Electric Power Research Institute. Electric Power Research Institute, Physical and Hydraulic
Properties of Fly Ash and Other By-Products from Coal Combustion, Product ID:
101999. February 1993.
Electric Power Research Institute. A Field and Laboratory Study of Solute Release from
Sluices Fly Ash, Product ID: 104585. December 1994.
Electric Power Research Institute. Coal Ash Disposal Manual: 3rd Edition, Product ID:
104137. January 1995.
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Electric Power Research Institute. Comparison of Coal Combustion Products to Other
Common Materials: Final Report, Product ID: 1020556. September 2010.
Finkelman, R.B, in Swaine, D.J. and Goodzari, eds. Environmental Aspects of Trace
Elements in Coal. Kluwer Academic Publishers. 1995: 24-50.
Fleet, M. E. L. Preliminary Investigations into the Sorption of boron by Clay Minerals.
Clay Minerals. 1965; 6(3): 3-16.
Griffith, G.E., Omernik, J.M., Comstock, J.A., Schafale, M.P., McNab, W.H., Lenat, D.R.,
MacPherson, T.F., Glover, J.B., and Shelburne, V.B. 2002. Ecoregions of North
Carolina and South Carolina, (color poster with map, descriptive text, summary
tables, and photographs): Reston, Virginia, U.S. Geological Survey (map scale
1:1,500,000).
Geosyntec Consultants. (DRAFT) Preliminary Site Investigation Data Report-Addendum
No. 1, Conceptual Closure Plan, L.V. Sutton Plant, Project Number GC5592. July
2014.
Geosyntec Consultants. (DRAFT) Data Interpretation and Analysis Report, Conceptual
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