United States
           Environmental Protection
           Agency
Office of
Emergency and
Remedial Response
EPA/ROD/R04-91/101
June 1991
&EPA   Superfund
           Record of Decision:
           Velsicol Chemical, TN

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REPORT DOCUMENTATION 1" REPORT NO.       I 2.     3. Reciplent'a Acceaaion No.   
  PAGE        EPA/ROD/R04-91/101             
4. nUe and SubtiUe                      S. Report Date      
SUPERFUND RECORD OF DECISION             06/27/91     
Velsicol Chemical, TN                6.        
First Remedial Action                        
7. Author(a)                        8. Perfonning OrganlZ8l1on Repl No.   
9. Perfonnlng Orgalnlzation Name and Addreaa                10. Project/Ta8k/Work Unit No.   
                         11. Contrscl(C) or Grant(G) No.   
                         (C)        
                         (G)        
12. Sponsoring Organization Name and Addreaa                13. Type 01 Report & Period Covered   
U.S. Environmental Protection Agency          800/000     
401 M Street, S.W.                         
Washington, D.C.  20460               14.        
1 S. Supplementary Notea                            
16. Abstract (limit: 200 won!s)                           
The 242-acre  Velsicol Chemical site is a former plant waste landfill located near the
city of  Toone,  Hardeman  County, Tennessee. Land use in the area is predominantly 
agricultural  with a wetlands area, 26 residences, and numerous creeks  located within
1 mile of  the site.  In  addition, part of the  site overlies a surficial aquifer that
was used as a potable water supply in the area.  From 1964 to 1973, Velsicol Chemical
Corporation used the site to dispose of  industrial and chemical  plant  wastes.  Waste
was disposed of in trenches excavated on 27 acres of the property. The site was  
closed in  1973  because  of the possibility of contaminated ground water migrating  
offsite.  By  late 1978,  State and Federal investigations had  confirmed ground water
contamination in private wells, and a public water supply  was provided in early 1979.
In 1980, a  35-acre low  permeability clay cap was placed over  the disposal area  to 
control  and minimize additional impacts  from the site. This  Record of Decision (ROD)
addresses  offsite ground water contamination,  as Operable  Unit 1 and will prevent 
additional  onsite ground water contamination from migrating from the disposal areas.
Future RODs will address other site contamination and principal  threats. The primary
(See Attached Page)                         
17. Document Analysia L Descriptors                         
Record of Decision - Velsicol Chemical,  TN              
First Remedial Action                        
Contaminated Medium: gw                      
Key Contaminants: VOCs (carbon tetrachloride, chloroform, toluene, xylenes),   
         other organics (pesticides)             
b. Identifiers/Open-Ended Terma                 
c. COSA n Reid/Group                            
18. Availsbility Sistement                19. Security Class (Thia Report)    21. No. 01 Pagea  
                       None     72   
                     20. Security Claaa (Thia Page)    22. Prtce   
                       None         
See A  9.18               Iructi               I 272 (4-77)
50272.101
NSI Z3
See Ins
ons on Reverse
(Formetly NTlS-35)
Department 01 Conwnerce

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EPA/ROD/R04-91/101
Velsicol Chemical, TN
First Remedial Action
Abstract (Continued)
contaminants of concern affecting the ground water are VOCs including carbon
tetrachloride, chloroform, toluene, and xylenes; and other organics including
pesticides.
The selected remedial action for this site includes installing extraction wells onsite
and offsite to restore the contaminated ground water to acceptable drinking water
standards; constructing an onsite ground water treatment plant and treating
contaminated ground water using solids removal, air stripping, and final ground water
polishing prior to discharge; discharging the treated water onsite to nearby surface
water bodies; treating off-gases with carbon adsorption; monitoring ground water;
maintaining the ground water treatment system and the disposal area cover; and
implementing institutional controls including deed and ground water use restrictions.
The selected remedial action is contingent upon the performance data collected during
operation. If the selected remedy cannot meet the specified remediation goals,
contingency measures may include alternating pumping at wells to eliminate stagnation
points; pulse pumping at wells to allow aquifer equilibration and encourage adsorbed
contaminants to partition into ground water; and installing additional extraction wells
to facilitate or accelerate cleanup of the contaminant plume. The estimated present
worth cost for this remedial action is $11,644,000, which includes an annual O&M cost
of $696,000.
PERFORMANCE STANDARDS OR GOALS: Chemical-specific ground water clean-up goals are
based on SDWA MCLs and health-based criteria, and include carbon tetrachloride
0.005 mg/l (MCL), chloroform, 0.006 mg/l, toluene 1 mg/l (MCL), and xylenes
10 mg/l (MCL). .

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9
0001
SUMMARY OF REMEDIAL ALTERNATIVE SELECTION
RECORD OF DECISION
REMEDIAL ALTERNATIVE SELECTION
VELSICOL/BARDEHAN COUNTY LANDFILL
GROUNDWATER, OPERABLE UNIT I
TOONE, TENNESSEE
PREPARED BY:
U.S. ENVIRONMENTAL PROTECTION
REGION IV
ATLANTA, GEORGIA
AGENCY
,.

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UUuL
RECORD OF DECISION
Remedial Alternative selection
First operable Un~t
S:TE NAME AND LOCATION
Velslcol/Hardeman County Landfill
rlrst operable Unit (Groundwater)
Toone, Tennessee
STATEMENT OF BASIS AND PURPOSE
ThlS decision document presents the selected remedial action for the
Groundwater Operable Unit of the velsicol/Hardeman county Landfill site in
Toone, Tennessee developed in accordance with CERCLA, as amended by SARA, and
to the extent practicable, the National Contingency Plan.
ThlS decision is based upon the contents of the Administrative Record for the
velslcol/Hardeman County Landfill site.
The United States Environmental Protection Agency and the State of Tennessee
agree on the selected remedy.
ASSESSMENT OF THE SITE
Actual or threatened releases of hazardous substances from this site, if not
addressed by implementing the response action selected in this Record of
Decision ("ROD"), may present an imminent and substantial endangerment to
public health, welfare, or the environment.
DESCRIPTION OF THE SELECTED REMEDY
Th~s operable Unit is the first of at least two that are planned for the site.
This operable unit remedy addre.ses remediation of the on-site and off-site
groundwater contamination by eliminating or reducing the risk. posed by the
slte through treatment, engineering and institutional controls.
The major component. of the selected remedy include:
Install and maintain approximately five extraction wells along the
northern boundary of the disposal areas located within the site
developing a hydraulic gradient to prevent groundwater contamination
above MCLs from leaving the disposal area.
Install and maintain approximately ten extraction wells into the
off-site groundwater contamination pl~ to control the groundwater
contaminant migration and remediate the groundwater off-site to MCLs.
Build and operate a groundwater treatment system for the removal of
contaminants from the extracted groundwater to NPDES requirements prior
to the water being discharged to a nearby surface water body. The
groundwater treatment is expected to be performed using, at a minimum,
settling tanks for precipitation of dissolved solids, an air stripper
and a carbon adsorption system.
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Monitor groundwater contaminant levels to verify that remediation goals
are reached.
Impose groundwater use restrictions for the affected area and post
appropriate hazardous waste disposal signs on and around the site.
Maintain the disposal area including fences and soil cover.
Identify and evaluate possible ~dditional remedial actions (Operable
units) required for addressing the contamination of the entire site
including the contaminant source (the disposal areas) and possible
environmental/ecological concerns.
STATUTORY DETERMINATIONS
The selected remedy is protective of human health and the environment, complies
with Federal and state requirements that are legally applicable or relevant and
appropriate to the remedial action and is cost-effective. This remedy utilizes
permanent solutions and alternative treatment (or resource recovery)
technologies, to the maximum extent practicable, and satisfies the statutory
preference for remedies that employ treatment that reduces toxicity mobility,
or volume as a principal element.
As this remedy will initially result in hazardous substances remaining on sit,
above health-based levels, a review will be conducted within five years after
the commencement of remedial action to ensure that the remedy continues to
provide adequate protection of human health and the environment.
~fY}JM;~

~Greer C. Tidwell
1- Regional Administrator
Date
..
.

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SUMMARY OF REMEDIAL ALTERNATIVE SELECTION
RECORD OF DECISION
REMEDIAL ALTERNATIVE SELECTION
VELSICOL/BARDEMAN COUNTY LANDFILL
GROUNDWATER, OPERABLE UNIT I
TOONE, TENNESSEE
PREPARED BY:
U.S. ENVIRONMENTAL PROTECTION
REGION IV
ATLANTA, GEORGIA
AGENCY
..

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SECTION
III.
IV.
VI.
VII.
VIII.
9
0005
TABLE OF CONTENTS
PAGE
I.
INTRODUCTION. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
II.
SITE NAME,
LOCATION AND DESCRIPTION........................ 1
SITE HISTORY AND ENFORCEMENT ACTIVITIES....................2
HISTORICAL LANDFILLING PRACTICES...........................2
INVESTIGATIONS AND STUDIES COMPLETED TO DATE.......
. . . . . . . .5
HIGHLIGHTS OF COKHUNITY PARTICIPATION......................5
V.
SCOPE AND ROLE OF RESPONSE ACTION..................
. . . . . . . .6
SUMMARY OF SITE CHARACTERISTICS.............................7
GEOLOGY AND
S'1'RA.TIGRA.PBY. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
HYDROGEOLOGY....
......................................... .11
NATURE AND EXTENT OF CONTAMINATION........................l7
SUMMARY OF SITE
RISKS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .'. . . . . 25
IDENTIFICATION OF CHEMICALS OF CONCERN....................25
EXPOSURE
ASSESSICEN'l'. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .25
TOXICITY ASSESSMENT......
.................................31
RISK CHARACTERIZATION..................................... 33
UNCERTAINTIES. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . J 9
ENVIRONMENTAL
RI Sits. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
DESCRIPTIOH OF ALTERNATIVES...............................42
ALTERNATIVE
1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .43
ALTERNATIVE
2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .43
ALTERNATIVE
3......... ....... . . . . . .... ........ ....... . ... .44
ALTERNATIVE
4.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .44
ALTERNATIVE
5. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .44
ALTERNATIVE
6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .46
.

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SECTION
XI.
XII.
9
OOC6
~ ~
TABLE OF CONTENTS (Cant'd)
PAGE
ARARs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
X.
SUMMARY OF COMPARATIVE ANALYSIS OF ALTERNATIVES...........49
SELECTED REMEDY........................................... 51
CONTINGENCY MEASURES...................................... 57
STATUARY DETERMINATIONS................................... 60
PROTECTION OF HUMAN HEALTH AND THE ENVIRONMENT............60
COMPLIANCE WITH ARARa..................................... 6 1
COST EFFECTIVENESS........................................ 62
UTILIZATION OF PERMANENT SOLUTIONS AND ALTERNATIVE
TREATMENT TECHNOLOGIES OR RESOURCE RECOVERY TECHNOLOGIES
TO THE MAXIMUM EXTENT PRACTICABLE.........................62
PREFERENCE FOR TREATMENT AS A PRINCIPLE ELEMENT...........62
...

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0007
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LIST OF FIGURES
FI GURE
PAGE
1
SITE LOCATION[[[2
2
DISPOSAL SITE[[[ 8
3
MISSISSIPPI EMBAYMENT........................................... 9
4
AREA CROSS SECTION............................................. 10
5
GROUNDWATER CONTOURS.......................................... .12
6
GEOLOGIC CROSS SECTION A-A'.................................... 13
7
GEOLOGIC CROSS SECTION 8-8'................................... .14
8
A-A'....."......................... .15
HYDROGEOLOGIC CROSS SECTION
9
HYDROGEOLOGIC CROSS SECTION 8-8'...............................16
10
FINITE ELEMENT MESH........................................... .19
11 CALCULATED CARBON
12 CALCULATED CARBON
13 CALCULATED CARBON
14 PREDICTED CARBON
TETRACHLORIDE DISTRI8UTION FOR YEAR 1990.....20
TETRACHLORIDE DISTRI8UTION FOR YEAR 2000.....21
TETRACHLORIDE DISTRI8UTION FOR YEAR 2010.....22
TETRACHLORIDE PROFILE.........................23
15
PREDICTED CHLOROFORM PROFILE................................... 24
16
COLLECTION DRAIN............................................... 45
17
COMPLI.ANCE. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
POINT OF
18
CO~ONENTS . . . . . . . . . . . . . . . . . . . . . . . . . . . .53
ALTERNATIVE 2 - REMEDIAL
19

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0008
9
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LIST OF TABLES
':'ABLE
PAGE
SUMMARY OF WASTE DISPOSAL.................... .... ........ .... ...4
2
EXPOSURE POINT CONCENTRATIONS................................. .18
3
FUTURE EXPOSURE POINT CONCENTRATIONS...........................28
4
CLOVER CREEK WATER CHEMISTRY................................... 29
5
PUGH CREEK WATER CHEMISTRY...... ...... ..... ..... ... ........... .30
6
FUTURE CLOVER CREEK CHEMISTRY..................................32
7
SUMMARY OF TOXICOLOGY AND CHEMICAL CONSTANTS...................34
8
SUMMARY OF GROUNDWATER CANCER RISK AND RA2ARD INDEX............37
9
SUMMARY OF SURFACE WATER CANCER RISK AND HAZARD INDEX..........38
10
SUKHARY OF FUTURE GROUNDWATER CANCER RIS~ AND HAZARD INDEX.....40
11
SUKHARY OF FUTURE SURFACE WATER CANCER RIS~ AND HAZARD INDEX...41
12
GROUNDWATER REMEDIATION LEVELS................................. 47
13
IN-STREAM DISCHARGE LEVELS..................................... 48
14
EVALUATION OF GROUNDWATER REMEDIAL ALTERNATIVES................52
15
REMEDIAL COST ESTIMATE - ALTERNATIVE 2.........................58
16
REMEDIAL COST ESTIMATE - ALTERNATIVE 6.........................59
APPENDIX A - RESPONSIVENESS SUMMARY
APPENDIX B - LETTERS FROM SUPPORT AGENCIES
APPENDIX C - RIS~ ASSESSMENT CERTIFICATION
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9
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RECORD OF DECISION
SUMMARY OF REMEDIAL ALTERNATIVE SELECTION
VELSICOL/HARDEKAN COUNTY LANDFILL
GROUNDWATER, OPERABLE UNIT I
TOONE, TENNESSEE
INTRODUCTION
The Velsicol/Hardeman County Landfill was proposed for inclusion on the
National Priorities List ("NPL") in December of 1982 and was finalized onto the
NPL in September of 1983. On 242 acres in Hardeman County, Tennessee, Velsicol
Chemical Corporation operated the 27 acre landfill for the disposal of plant
waste generated at their Memphis, Tennessee plant. The Remedial Investigation
("RI") report which examines air, sediment, soil, surface water, and
groundwater ~ontamination was completed in April 1991. The Operable Unit I
Feasibility study ("FS") which develops and examines alternatives for
remediation of the groundwater was submitted to the public information
repository with the RI Report in April of 1991.
This Record of Decision ("ROD") has been prepared to summarize the remedial
alternative selection process and to present the selected remedial alternative,
in accordance with Section 113(K)(2)(B)(V) and Section 117(b) of the
Comprehensive Environmental Response, Compensation, and Liability Act of 1980
("CERCLA"), as amended by the Superfund Amendments and Reauthorization Act
«"SARA") P.L. 99-499). The Administrative Record for the velsicol/Bardeman .
county Landfill Site forms the basis for the Record of Decision contained
herein.
SITE NAME. LOCATION. AND DESCRIPTION
The Velsicol/Bardeman County Landfill is located on an approximately 242-acre
parcel approximately one mile north of Tennessee State Bwy 100 on the east side
of Toone-Teague Road (see Figure 1). The Velsicol/Bardeman County Landfill and
the contaminated areas associated with the landfill will hereinafter be
referred to as the "Site".
The 242-acre parcel was purchased by Velsicol Chemical corporation ("velsicol")
for use as a landfill and is presently owned by a hOlding company for
Velsicol. From 1964 to 1973, the landfill was operated by Velsicol for the
disposal of their Memphi., Tennessee pesticide manufacturing plant's production
waste.
Waste from the plant was di8posed of in trenches excavated on 27 acres of the
property (the "di8posal areas"). The top 'of the disposal areas i8 generally
flat; however, the 8ide8 of the dispo.al areas slope down toward the drainage
areas and creek.. The di8posal areas are located on the we8t side of Pugh
Creek and are approximately one mile south of clover Creek which contains a
large wetlands area. The creeks are used recreationally but are not used as a
drinking water source.
The Sit. is locat.d in a rural part of Bar4eman County, Tenn..... and most of
the land use in the ar.a i8 agricultural. Groundwater beneath the Site
property is encountered at approximately 30 feet below land surface down to a
depth between 110 to 170 feet. An artesian aquifer i. locate4 at approximately
220 feet below land .urface. The surficial aquifer beneath the Site property,
comprised of the Wilcox and Claiborne Formation., was u..~ a. a potable water
-8upply in the area. Approximately 26 re.idence. are locat.d within 1 mile of
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SITE lOCATION - VElSICOUHARDEMAN COUNTY LANDFilL
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9
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the disposal areas with the nearest residence within one-quarter of a mile from
the disposal areas.
Due to the disposal of the industrial and chemical wastes in the disposal
areas, government agencies and the nearby community have raised concerns
regarding potential impact from the Site.
SITE HISTORY AND ENFORCEMENT ACTIVITIES
Historical LandfillinQ Practices
In July 1964~ velsicol purchased the
Tennessee, specifically for use as a
Velsicol's Memphis, Tennessee plant.
by the Toone-Teague Road to the west
242 acres of land in Hardeman County,
landfill to dispose of plant waste from
The property, shown on Figure 1, is bound
and pugh creek to the east.
Immediately 'upon purchasing this property, velsicol began erecting a fence
around a portion of the property where the landfilling was to commence. The
purpose of the fence was to prevent local livestock from wandering onto the
area during active landfilling. The fence ~as comprised of three strand barbed
wire. A gate was provided at the access point off of the Toone-Teague Road.
The landfilling operation commenced in October 1964 and continued until June'
1973. At the time of closure, waste had been disposed of in three specific
disposal areas which covered a total area of approximately 27 acres. It was
initially estimated that an equivalent of. approximately 300,000 drums of plant
waste from Velsicol's Memphis plant were dispo8ed of in these three disposal
areas. During the development of the RI work Plan, velsicol completed a more
detailed estimate of waste volumes based on extensive evaluations of detailed
plant production rates. A more accurate estimate of waste quantity and type,
based on this second review by velsicol, is summarized in Table 1.
Development of the landfill began in October 1964 with the northern disposal
area since it was the only area on the property which was cleared of trees.
Waste disposal commenced along the east side of the north disposal area and was
carried out. longitudinally in the direction of the property ridges. The middle
and south disposal areas were developed sometime in the late 1960s or early
1970s. Subsequent to a public meeting held in Jackson, Tennessee in March
1971, the Tennessee Department of Health and Environment (-TDBE-) evaluated the
landfilling operation at the site. On the basis of this evaluation, a
Commissioner's Order was issued to Velsicol by TDBE which required Velsicol to
cease disposal operations in the south disposal area in August 1972, but
allowed limited waste disposal in the middle and north disposal areas until
June 1973. Therefore, after closure of the south disposal area, selected
wastes continued to be disposed of in the north and middle disposal areas until
the landfill was permanently closed in June 1973.
Plant waste was disposed of in trenches which were excavated longitudinally
along the top of the property ridges. Velsicol's records indicate that each
trench was excavated to a depth of 12 to 15 feet~ to a width of 10 to 12 feet~
and to a length of 200 to 500 feet. Trenches were placed approximately four to
eight feet apart.
As each transport vehicle arrived at the disposal areas, the containerized
waste was dumped off the truck into one of the excavated disposal trench.s.
,.

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     IAIIIII     
   SUMMAUY 01 WASil. IHSI'OSAI. AI IIAIU)J:MAN ( (II IN I) I ANIIIIII   Ul
    IIAIWI:MAN COUNT\' I.ANDHI.I. Hili S    
          \,.Q
   Weight T(lt~1 Tot~1    1 'I '", ,,1"111 . 
   Utllsity Wtigh' Vol","t [qllil)ala-,,' M..,""" ..f I'""",. C)
 IV/lslt'  (lbslgal) (/bs' (Gal) , of "rulllS of III "/'" ,,1 , ,",,11111,'/ 0
          -~
 I h'pl,H:hlor Catalyst 111.1 2,539,000 251,386 4,571 II  1 ',/I 1'0
 Ilcplanc Hl'sidul' 6.3 14 .5)1), 1100 2.)07,778 4 I ,IJ(,() 1/11   
 hl)l'r Drums     45,417 II  4',..11/ 
 \I' A Still D- 30 Bolloms 12.0 16,128,000 I,J44,OOO 24,43h °1/1\  I\KH I 
, AN2K    994,605 18,004 1/ II   
 Acclic Acid 80110015 19.9 19,351.1I()O 972,412 17,68() °1/11  11..1'11 
 H.' 2 Bol\oms  7.1 D,854,94() 1,951,400 35,480 °l/ll/~)  2 1.f)It.> 
 (hlon-ndic Anhydride        
 SIIiI Uotloms 10.8 10,1 25,O()0  937,500 17,045 01/11  11.11/'1 
 I'CL Bollums )-11 14.1 n,988,(X)() 9'J2,057 18,037 01/11  II,!! I  
 Carbon 8t.-ds  9.4 1,515,1X)() 161,170 2,930 If  1." Itl 
 HanJanc Filter Cakc 15.6 3,122,000 200,128 3,639 If  1.1t 19 
      -    
    95,161,940 10,112,436 229,279   129.;"// 
NotC$:
II .'
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II
Disposal by landfillint; al I larJeman Counly Landfill
Disposal by mum'r.IIIOII ..1 Ml'ml'his 1'1.1111 S,ll'
I )ISPUSl'J as Iud ill pl.1I11 hoilt'r
I ),sposal by Jisch.nglllg to Iht' Itlt.al s.lIIilJry sl'wer
W.lsll' d,SI)(,<,t'd 01 hy IIWllIl'rJllon II0wt'vI'r, WIU'IIIIICIfH'r.,'or WdS nol oper.llm!; (It', I','n ,'nl 011..111'/. w.I',I,' dl"I~,'.,,1 11/1'1'
..1 'IMd"III.ln (.o""ly 1.11,.11111
1.111.11 II III "'.
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0013
On occasion; drums were set upright in the trenches upon disposal. In most
cases, however, the containerized waste was left in the trench in the random
order and orientation of which it had been dumped. Disposed waste. was covered
daily with soil excavated from the trenches. Upon filling with waste, each
trench was covered with a minimum of three feet of soil which had previously
been excavated from the area. The cover material was placed and compacted with.
a bulldozer and was mounded over the backfilled trenches to allow for future
settlement. periodically, as the backfilled areas settled, repairs were made
by backfilling with additional soil.
Investiqations and Studies comcleted to Date
Investigative studies at the site were started as early as 1967 when the United
States Geological Survey ("USGS") reported on the potential of the disposed
wastes to contaminate the groundwater beneath the disposal areas. Findings of
these studies lead to the above-referenced commissioner's order limiting
additional disposal in the trenches and finally closing the disposal areas in
1973. By late 1978, state and Federal investigations had confirmed groundwater
contamination in private wells. The use of wells by residences in the vicinity
of the disposal areas for domestic water supply was halted, and in early 1979,
a public water supply replaced the private drinking water wells. In 1980,
based on studies prepared by the united states Environmental Protection Agency
("USEPA"), TDRE, USGS and contractors working for velsicol, a low permeability
clay cap covering approximately 35 acres was placed over the disposal areas to
control and minimize additional impacts from the site.
After the completion of the cap, a monitoring program was implemented by
Velsicol and overseen by USEPA and TDRE to assess the effectiveness of the
cap. The monitoring program included the regular monitoring of groundwater
quality, surface water and sediment quality in pugh and clover creeks, a
regional groundwater elevation survey surrounding the Site and the installation
of lysimeters beneath the clay cap.
In December 1982, the site was proposed for inclusion on the NPL. The results
of the monitoring program were presented in February of 1985, and on November
5, 1985, TDRE issued a notice to Velsicol stating that a Remedial
Investigation/Feasibility study ("RI/FS") would have to be performed for the
site. USEPA and TDRE entered into a site Enforcement Agreement in July of 1986
making TDRE the lead agency responsible for enforcing the remedial activities
performed at the site. On January 7, 1987, TDRE issued a commissioner's order
requiring velsicol to perform the RI/FS for the site. In late 1988, EPA Region
IV became the lead agency, and in February of 1989 entered into an
Administrative order on Con.ent with Velsicol to complete the RI/FS. The RI
and FS reports were completed in early April of 1991 and were placed in the
information repository along with the Administrative Record ("AR") prior to
April 15, 1991.
HIGHLIGHTS OF COMMUNITY PARTICIPATION
I
During the early 1980s, numerous community relations meetings were held to
address community concerns. After contaminated well usage was replaced with
public water, and the landfill was covered with the low-permeability cap, the
community was informed through fact aheets, information placed in the Site
repository, and contact with State and Federal officials.
,..

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~
5
9
00'1 4
In February of 1988, as part of the RI, a Community Relations plan ("CRP") was
prepared by the TDHE with assistance from the university of Tennessee. This
document lists contacts and ~nterested parties throughout government and the
local community. It also establishes communication pathways to ensure timely
dlssemination of pertinent information. Based on the CRP, a public meet~ng was
held to discuss the RIfFS process with the community.
In April of 1991, the RIfFS and the Proposed Plan for the groundwater operable
Un~t ("Proposed Plan") were released to the public.
All of these documents were made available in the Administrative
at USEPA, Region IV and the information repository maintained at
aol~var-Hardeman County public Library.
Record located
the
A public comment period was held from April 25, 1991 to May 24, 1991. In
add~tlon, a public meeting was held on April 25, 1991 to present the results of
the RIfFS and the preferred alternative as presented in the Proposed Plan. All
comments which were received by USEPA prior to the end of the public comment
per~od, including those expressed verbally at the public meeting, are addressed
in the Responsiveness summary which is attached, as Appendix A, to this Record
of Decision.
SCOPE AND ROLE OF RESPONSE ACTION
The scope of this response action is to address the off-site groundwater
contamination and prevent additional contamination from leaving the disposal
areas via migration through the groundwater. This response action is the first
of two or more operable units ("OP unit") or remediation phas.s that will be
used to address the contamination of the entire sit. including the landfill
wastes and any long term environmental effects caused by the migration of waste
from the disposal areas. The preferred alternatives for the groundwater OP
Unit ("OP unit t1") will address the remediation of contamination in the
groundwater beyond the disposal areas boundaries prior to its discharge into
the nearby surface water bodies of Clover and Pugh creeks.
A remedy for the groundwater is proposed to protect public health and the
environment by controlling exposure to the contaminated groundwAter and
controlling migration of the contamination through the groundwater to soils,
sediments and surface water bodies. The groundwater is being addressed first
for a number of reasons I
1.
Contaminants in the groundwater are above Maximum Contaminant Levels
(-MCLS-) for drinking water and pose a health risk for anyone using
the groundwater. presently, homes in the area are being supplied
water due to the groundwater contamination.
2.
Groundwater treatment can be started while additional studies are
performed and evaluated. These additional studies are required for
determining remediation technologies for controlling the source are
performed And evaluated.
3.
Groundwater
bodies, and
creeks over
is presently discharging into
higher levels of contaminants
the next four years.
the nearby surface water
will be discharging to the
-

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-7 -
5
9
0015
Future response actions will address other Site contamination and principal
threats completing remediation of the entire site.
SUMMARY OF SITE CHARACTERISTICS
The source of the Site contamination including the groundwater is the 27-acre
waste disposal areas (see Figure 2) located within the site.
sampling of the disposal areas, nearby soils, surface water, sediments and
groundwater was performed during the Remedial Investigation ("RI"), and the
results of the sampling are contained in the April 1991 RI report. This Record
of Decision for OP unit t1 will address only the results of the groundwater
portion of the RI since additional studies are required to evaluate final
disposal area remedies.
Geoloqy and stratigraphv
The site is located on the eastern flank of the Mississippi Embayment (see
Figure 3). The embayment is a thick suite of sediments deposited in a large
syncline or geologic trough, covering approximately 100,000 square miles in the
Gulf Coastal plain. The axis of the syncline plunges to the south, Le. the
sediments thicken to the south, with its axis roughly following the Mississippi
River. A cross section of -the area is shown in Figure 4.
The Porter's Creek clay is a thick sequence, averaging approximately 120 feet
of largely gray to black Paleocene clay, with noncontinuou8 subordinate lenses
of sand. This sequence of clays effectively seal. off the lower formations
from any contamination in the overlying Wilcox and claiborne (Eocene)
Formations.
The wilcox Formation unconformably overlies the Porter's creek clay, i.e. there
is an erosional break between the two :ormations. The Wilcox, estimated to be
75 to 125 feet thick in the .tudy area, ia a heterogeneou. unit of sand with
some silt and clay, with occasional beds of lignite, kaolin, and siderite
(FeC03). Theae sediments are interbedded and interlensed, and are not
laterally persistent. They are typical of nonmarine fluvial or deltaic
depoaita. This lack of lateral continuity is one of the key factors in
questioning the ability of the formations to receive continuous reinjection of
treated groundwater at tbe site.
The claiborne Pormation ia similar to the wilcox witb many vertical and
horizontal di.continuitie.. The Claiborne is comprised predominantly of
interbedded .and. with len.e. and thin bed. of clay and sandy clay, and 80me
thin len... of kaolin. It. maximum thickne.. in we.tern Tenne..ee is up to
1100 feet, but in the .tudy area it range. from 0 to 125 feet.
The Wilcox-Claiborne contact uaually is not discernible in Tennessee because
(1) the lithologies are similar, (2) th. stratigraphies of th. two formations
are so variable, and (3) the boundary between the two is erosional and,
therefore, not at all uniform.
Quaternary alluvial sediment. overlie mo.t of the Claiborne Formation in this
area. Thi. alluvium ia similar to the Claiborne .ediments and could not be
differentiated from them in the study ar.a. The alluvium i. usually capped by
,.

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5 9
0016
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0019
loess, which is glacially derived, wind blown, very anqular silt. silt was
present at the surface at 9 of 12 well locations drilled near the Site. The
thickness of the loess deposits ranges from 0 to about 12 feet.
HVdroaeoloQV
The Porter's Creek Clay is'an aquitard that forms the lower boundary of the
water table aquifer in northern Hardeman County. The sands of the Wilcox and
Claiborne Formations are hydrologically connected and form one
hydrostratigraphic unit as the water table aquifer. This aquifer ranges from
approximately 6S to 12S feet thick in the study area and is considered a Class
IIa aquifer,'
Precipitation is the principal source of groundwater recharge. On a broad,
regional scale, movement of groundwater generally follows the dip of the
sediments, which is to the west toward the Mississippi River. Flow directions
within the water table aquifer in the outcrop area, such as at the Site, are
primarily controlled, however, by the local topography and nearby stream
systems. Clover Creek and the Hatchie River are the primary discharge areas
for the water table aquifer in northern Hardeman county, with Clover Creek
establishing the direction of groundwater flow to the north and northwest in
the area of ,the site (see Fiqure S).
The water table aquifer is the primary source of groundwater in northern
Hardeman County. Cross sections from south to north are shown in Fiqures 6 and
7. Sand thicknesses are circled to indicate the many potential pathways for
contaminant movement through these heterogeneous strata. Although there are
many low permeability lenses, studies near the edge of the Site showed that
perched water on top of these lenses is seldom found.
Corresponding well placements and the elevations of the groundwater and ground
surface are shown in Fiqures 8 and 9. At the disposal areas, contaminants have
to diffuse and percolate through 7S to 9S feet of sediments in the unsaturated
zone before they reach the groundwater. A two-foot thick clay cap installed on
the disposal areas in 1980 has sUbstantially reduced percolation through the
trenches and waste.
Although private wells in the vicinity of the disposal areas were monitored
extensively during the early phases of groundwater contamination, these wells
have been largely abandoned or plugged after Velsicol provided for an
alternative water supply to the residences affected by the downgradient
contamination. All groundwater monitoring is now done from carefully installed
and logged monitoring wells.
Vertical hydraulic gradients were calculated for each monitoring well nest.
Well nests are indicated schematically on Fiqures 8 and 9 by multiple screens
at the same location. Downward gradients ranging from 0.0004 to 0.02 feet/foot
were found at five of the eleven locations: while upward gradients ranging from
0.002 to 0.18 feet/foot were determined at the remaining six wells. The
relatively low magnitudes of the downward gradients adjacent to Pugh and Clover
creeks, however, suggests that horizontal flow parallel to and beneath the
creeks is occurring in Scme reaches. The complete groundwater and surface
water elevation data support the conclusion that these creeks form the
hydrologic boundaries of the groundwater flow from the Site. '
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    5
    9
    -17-
    0025
    Nature and Extent of Contamination
    In monitoring the downgradient movement of contaminants beyond the disposal
    areas, only carbon tetrachloride (CCI4) and chloroform (CBCI3) were detected in
    1989 in all six samples from two rounds of sampling (in samples from each of
    three selected downgradient wells as shown in Table 2).
    Contaminants detected in five of the six samples were acetone (which may. have
    been a result of laboratory contamination), methylene chloride, and
    tetrachloroethylene.
    Two contaminants were detected in four of the six samples:
    chlorobenzene and toluene.
    These mobile contaminants are all volatile organic compounds ("VOCS")
    characterized by:
    high vapor pressures,
    moderate to high solubilities,
    relatively high Benry's Law constants (partitioning between air and
    water), and
    relatively weak sorption to soil organic matter.
    Pesticides and related compounds were either not found at all in the
    groundwater or were mainly found in the groundwater on-site.
    Groundwater flow and contaminant transport were modeled with a two-dimensional
    integrated depth model, GWPGK3, developed by J. F. Sykes at the university of
    Waterloo, Waterloo, Ontario, in 1987. This is a finite element, numerical
    model used for two-dimensional analyses of steady state flow and mass transport
    in variably saturated cross-sections and integrated depth confined or phreatic
    (water table) aquifers. .
    The finite element mesh used for the model is shown in Figure 10. Simulations
    of predicted carbon tetrachloride concentrations are shown in Figures 11 to 13,
    with a predicted concentration profile shown in Figure 14. similar
    distributions of chloroform were developed; its concentration profile is shown
    in Figure 15.
    While the model was calibrated against measured contaminant concentrations in
    the field, these modeling results can only be interpreted qualitatively. The
    heterogeneous nature of the geology of the area precludes an accurate
    prediction of future conditions, which must be modeled from the assumptions of
    hydraulic conductivity, longitudinal and transverse dispersivity, etc. Using
    these assumptions, the calibrated hydraulic conductivity used in the model was
    O.OOS cm/sec. This value is significantly lower than the maximum value of
    0.0111 em/see as determined by slug tests. Yet even the value of 0.0111 em/see
    resulted in a calculation of a travel time of approximately 26 years for
    groundwater beneath the disposal areas to reach Clover Creek; whereas the
    actual travel time was l.s. than 23 years. The actual tran.port time must
    necessarily be the result of groundwater flow through the many interconnected,
    highly permeable sand lenses highlighted in Figure. 6 and 7.
    ~
    

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    '"' 9 0026 TABLE    
    '-' -   
       EXPOSL"RE POI~-r CO~CE~'TRATION (mg/lJ  
    GROL;..L>WATER. OOW~GRADrr::-..-r PtL~  
       HARDE.'.{A."i COL':-..n LA~1JmL RIfFS  
         .  
        Round 1   Round:
    CkLmlcal CM.5 IJ C,\fJ'.5 GM.5 13 C,',fP-j
    .o...:erone   3.38 758 0.021 1.68 ~ ~~ :x
      ' j
    -:JrtxJn 7' etrac....londe :.76 '" -... :.19 1:.0 505 :: ':8
    ..:: I
    C hiorobenzene 0.009 0.038 0.00 0.006 0.051 ,J)J
    C;uorororm O. 707 0.914 0.807 .., ~- :.09 : :-~9
    _.~,
    \lethvlene C:-Uonde 0.503 0..91 0.00 a.:~ 054: -. ,""" ("\,
    ... """ j, v
    -:- errac!-joroethvlene 0.014 0.0:1 0.00 0.010 0036 = J06
    7oiue1"e   0.11.5 0.302 0.00 0.095 0...01 000
    Xvle1"e   0.00 0.007 0.00 0.00 0.00 0.00
    3is(: ethvlhexyDphth..1.l.1te 0.00 0.00 0.200 0.087 0.00 0 . ()()
    :JI-n-butvlphttaare 0.00 0.00 0.00 0.00 0.00 J:xJ
    :Jt-n-octy! ph thalate 0.00 0.00 0.010 0.00 0.00 'JJO
    : 4- :>1 c.....lorop henol 0.00 0.00 0.00 0.00 000 ' ':-\
    . ,\.:
    Endnn   0.00 0.00 0.00 0.00 000 :X
    Endnn ketone 0.00 0.00 0.00 0.00 0.00 J),;
    Endr:n Aldehyde 0.00 0.00 0.00 0.00 0.00 JX)
    Heptachlor 0.00 0.00 O. (XX}2 0.00 0.00 Joo
    .
    I'-ELL LOCU IO~S ARE SHJ\\i\ ON FI GUR:: 11
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    (.;,!
    I'V
    - --------" ----
    - ----~ WEll.GM 5
    WEllll
    /
    "
    '-
    
    . . . . . ' " ~ . . ' ~~/ WEU'GMP 5
    
    
    
    ,--- . -------- -- - -~ ~';~~.,
    
    
    -~ - ~ .~~=--'--'""--=--c-
    /
    /
    /
    /
    /
    /
    /
    /
    /
    /
    /'
    -----~----
    -- -
    1975
    2UIO
    2015
    1985
    1995
    2lX)()
    2()(J5
    19811
    1990
    -, illl~ (yurs)
    figure I',
    PREDICTED CHLOROFORM CON CENTRA TION PROFilE
    Ve/sicol Chemical Corporation
    

    -------
    5
    -25-
    9
    0033
    SUMMARY OF SITE RISKS
    A baseline risk assessment was conducted for the Site and is presented in the
    RI report. The risk assessment consisted of a chemicals of concern
    identification, an exposure assessment, a toxicity assessment and a risk
    characterization for human health effects.
    Environment risks were briefly discussed based on available data; however,
    additional information is required, and an environmental evaluation will be
    conducted as a part of OP Unit 42.
    Identification of Chemicals of Concern
    The identification section involves the selection of the contaminants of
    concern ("COCS") used in evaluating the risks associated with the Site. The
    COCs are detected cont~inants which have inherent toxic/carcinogenic
    properties that are likely to pose the greatest concern with respect to the
    protection of public health and the environment. Selected contaminants of
    concern at the Site include:
    Carbon tetrachloride
    Chlorobenzene
    Chloroform
    Tetrachloroethene
    Toluene
    Xylene
    Acetone
    Methylene Chloride
    Bis (2-ethylhexyl)phthalate
    Di-n-butyl phthalate
    Di-n-octyl phthalate
    2,4-Dichlorophenol
    Enarin
    Enarin Ketone
    Enarin Aldehyde
    Heptachlor
    All of the contaminants above except Methylene Chloride and 2,4 -
    Dichlorophenol (which were detected only in groundwater) were detected in both
    soil and groundwater beneath the disposal areas.
    EXDosure Assessment
    The exposure assessment identified potential pathways and routes for
    contaminants of concern to reach the receptors and the e8timated contaminant
    concentration at the points of exposure. Contaminant release mechanisms from
    environmental media, based on relevant hyarologic and hyarogeologic information
    (fate and transport, and other pertinent Site-8pecific information, such as
    local land and water us. or demographic information), were also presented.
    At the Site, the current receptor population Was identified as limited to the
    residential community surrounding the disposal areas.
    Groundwater 'is the current release medium which can transport chemicals from
    the Site. Prior to capping the disposal areas in October 1980, direct contact
    with the waste and surface water transport Was a potential release medium.
    Bowever, the graded and grassed cap presently precludes any direct contact with
    wastes or erosion of wastes into surface water. The cap also limits air
    dispersion of volatile organic chemicals from the waste. The aquifer under the
    Site was the aquifer from which local residents' wel18 previously arew water
    for household use. Although the present residents now receive their household
    water from a public water supply, the potential to use the aquifer for
    residential water exists and thus has been evaluated as a potential exposure
    pathway. This pathway includes the consumption of contaminated groundwater and
    the inhalation of volatiles through bathing-
    ,.
    

    -------
    5
    -26-
    9
    0034
    The contaminated groundwater discharges to the surface either at seeps or
    d~rectly to Pugh and clover creeks. All of the identified continuous seeps
    presently flow into Pugh or clover Creek. Because of the remote locations of
    the seeps, direct human contact is considered unlikely. However, if contact
    d~d occur, it would most likely be single or occasional exposure resulting in
    an ~ns~gnificant total dose. Therefore, potential human exposure to the seep
    cor.tam~nation ~s considered to be via the surface water in Pugh and Clover
    Creeks.
    Because the volatile organics which are migrating from the site biodegrade and
    volatilize in open waters, they are not persistent in the above-ground
    env~ronment. This lack of persistence significantly limits their potential
    r~sk and hazard to human health when evaluating the surface water exposure
    pathway.
    Potential exposure to the water in pugh and Clover creeks is through
    recreational activities, primarily fishing and hunting. Although fishing would
    probably be limited to Clover Creek, since Pugh Creek is too shallow to support
    a game fish population of fishing size, data from both creeks has been
    evaluated. Game animals could drink from either Pugh Creek or clover creek.
    Human exposure would be limited to eating fish caught in clover Creek or eating
    game animals which might drink from the creeks. Although neither Pugh nor
    Clover creek would be expected to be used for swimming, a sw~ing scenario has
    been included in the assessment to conservatively address any occasional
    wad~ng, swimming, or water contact by residents.
    The following human exposure pathways were evaluated for potential exposure
    po~nt concentration., e.t~ated daily intake and potential risk andlor hazard:
    o
    the use of contaminated groundwater for household use,
    o
    recreational fishing and fish consumption from clover Creeks,
    o
    occasional skin contact while fishing, swimming, or wading, and
    o
    inhalation of volatile compounds detected in clover Creek while
    fishing.
    Three levels of as.umption. are presented for each .cenario. -Levell-
    assumptions pre.ent the average or mean value for the exposure assumption,
    -Level 2- pre.ents assumptions which will include, statistically, 90 to 95
    percent of the population, and -Level 3- pre.ents as.umptions that are
    considered maximum wor.t ca.e a..umption. which are individually po..ible. For
    example, occupancy of a re.idence at one location for 10 years i. considered
    to repre.ent the average length of tim8 that individual. will pre.ide at one
    location (-level 1-). The -90th- percentile value for length of occupancy for
    one residence is 30 year. (-level 2-). It i. pos.ible that an individual could
    spend their entire life in a single location so the Level 3 value is assumed to
    be 70 years.
    The mean of all .ample concentration., including non-detect. at half the
    detection limit, in the media being evaluated i. u.ed for the Levell
    calculations, and the statistical 95th percentile on this mean is applied for
    the Level 2 calculations. For the Level 3 calculation., the mean of only the
    analytically detected values is used as the applicable media concentration for
    .
    

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    5
    9
    0035
    -27-
    a possible maximum exposure. In those cases where a single well or sampling
    location is evaluated, the single value is evaluated using all three exposure
    levels of each applicable scenario.
    To evaluate the exposure to groundwater under present conditions, the reported
    concentrations of the chemicals of concern were evaluated in Wells GM-5, 13 and
    GHP-5 for sampling rounds 'in FebruarY/March 1989, November 1989, and November
    1989 (Table 2). Selection of these wells provides information on concentration
    along the approximate center line of the plume between the northern boundary of
    the disposal areas and the edge of Clover Creek.
    The concentrations of carbon tetrachloride and chloroform were estimated in
    wells GM-5, 13, 7 and GHP-5 for the years 1968-2011. Years 1995, 2000 and 2010
    were evaluated for potential risk and hazard. The calculated concentrations of
    carbon tetrachloride and chloroform in each of the four wells for these three
    time intervals are summarized in Table 3.
    The only expected human exposures to potential contamination in the surface
    water is by consumption of fish which have been exposed to contaminated water,
    the consumption of wild terrestrial animals ~hich may drink contaminated water,
    the occasional skin contact while wading or while fishing or the potential
    inhalation of volatile compounds which could potentially volatilize from the.
    surface water while fishing. .
    Tables 4 and 5 summarize the environmental data from Pugh and clover Creeks.
    only Clover Creek appears large enough to support a game fish population. Game
    animals could drink from either creek. The analytical data indicate that there
    is no consistency in the reported concentrations., Acetone,
    bis(2-ethylhexyl)phthalate, di-n-octyl phthalate, and endrin ketone are
    reported in upstream locations which are not impacted by the contaminated
    groundwater plume from the Site. Beptachlor, heptachlor epoxide and b-BBC were
    reported in only a single sample in the two sampling rounds. Based on the
    presence of pesticides in the upstream samples and the pattern of positive
    detects it presently appears that the pesticides detected in the creek water
    are not exclusively, if at all, from the discharge of contaminated groundwater
    from the Site.
    Carbon tetrachloride and chloroform are the only chemicals reported in the
    creeks which appear to be Site related. Although the.e volatile organics are
    migrating from the Site and may enter the creeks, their volatility and
    susceptibility to degradation apparently prevent their accumulation in the
    creeks at concentrations that are consistently detectable. Although the source
    is not definite, the concentrations of the volatiles reported in the creeks
    (Tables 4 and 5, Round 2) were evaluated for their potential exposure and
    estimated total incremental risk and hazard to human health.
    To evaluate
    Pugh creek,
    where water
    used Clover
    public health impacts of Site-related chemicals in Clover Creek and
    it was assumed that game fish were caught and consumed in areas
    contained Site-related chemicals and that the same individual also
    creek and Pugh Creek for recreational swimming.
    A scenario for potential exposure from
    which may drink the contaminated water
    concern which are discharging into the
    consumption of game animals and birds
    was not developed. The chemicals of
    stream tram the Site (carbon
    ,.
    

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    - -
    5 9
    0036
    TABLE 3
    
    ESTIMATED EXPOSURE POINT CONCENTRATIONS FOR GROt:~DWATER
    FtJTURE MODELED CONDITIONS. DOWNGRADIENT PLt.:ME
    HARDEMAN COt:~TY LA~"DmL RIIFS
    Well Year Carbon Tetrachloride ChIaro form
      (mgl L) (mgiL)
    GM-3 1995 10.989 :.S:~
     2000 6.689 1.029
     2010 2.513 0.33:
    13 1995 8.833 1 ~'''"'
    ..-""1'-
     2000 3.846 0.936
     2010 2.410 0.3::-
    .. 1995 7.654 1--*63
    I
     2000 3.892 1.003 .
     2010 2.7i1 0.387
    GMP-3 1995 3.526 ., .-~
    ;. . .. .J
     2000 3.025 0.9::-
     2010 2.7'23 8.39:
    ..
    

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    '-)
    0037
    TABLE :,
    CLOVU alEEJC WA1'U CHEMISTRY (~8ft)
    HARDEMAN COUNTY LANDFTLL R1IFS
    CJwMic.l
     RcnuuI I   Rown4 2 
    CII. C. Ob C4 CII. C. 06 C-I
    13.2 13.7  23-   
     .:J   
    .),.~erone
    .:..uOon Tea-achlonde
    13.67
    :3
    ::-.iorororm
    SIS\ :~th vlhexyl)?nt~te
    470
    :'\. n-«:~ipnthalare
    :.:'\c~rl
    0.224
    ~::C:-::'L KelCne
    0.32
    H et) laC !\lor
    0.172
    He?lachlor Epoxide-
    0.118
    Hexac.:.uoroc:ycloncun8 (b.;BHO-
    0.163
    .\,'otes:
    . :: . Locanons u!"num of Ira wnere contaminatKi downpdient piume discha~es to creek.
    ~, - COnSQN8nCl not det8l:18d llIanglKl banngs and nOt sei8C18d IS concaaunanCl or concern.
    .3) Other contamtnanCl or CDnC1!m not det8l:1l!d in Cover Creek lamples.
    ~
    

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    r-
    J
    9
    o CJ 38
        '7" AiLE      
      I"..:GH am W41"EJ. or£MISTlY (~    
      HAAOEM AN co l:NT'r LA .'lOFTU. R1I'FS    
      R""... 1     Ro",",,: 
    Pt' P"~' P'2b' PJ. P4 PS ;>6" P"'~" P'2b" P3,0" p,
     18.8  ~       
       44.9 ZS.9 51..3     :'
              .
     :::3         
     \00 31 \0 15 11     
    0.196 04 04 007 0..3.5      
    o..-ui
    ....:'~ne
    ~J"'tIOn -:-.r.ncniOnd.
    -=~cl"'Ororm
    3...,: -4lt1vI ncxvI ~rllna...
    ="n~lonthAu..
    ~ar./'I
    ~~cr./'I K.u:>,.,.
    '-"~QcNor
    -:~oac..""'or EooXJ~
    ,.,u...a'l\Joroevc:JOn.un. ,'t>-8Ha.
    "'C3 IArodor ::U).
    2.514
    '.0..
    .. , 9.ac~und 5A!IIot~ loc:nON ....",en ~ nOf rwc..... ~.....t.. tftIIft ~ s....
    :. - ~.xaDO/'l nor &naIV28I rhI8 n:Nnd.
    JI . w:>ruDNI'IU:I root aft8Cl8d '" ~18d bann~.nd nO( ~ .. contamlNna of oanam.
    .. 2!t1er ::::>/'IQI!Iln&r\1I 01 amarn not Cl8l8Cted 1/'1 Pu~n Crwu. 'AII'Ipt8.
    .
    

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    -31-
    5
    9
    0039
    tetrachloride and chloroform) would be metabolized and/or excreted from animals
    or birds. Due to the low levels of Site-related volatile compounds in the
    surface water samples, bioconcentration and tissue retention are expected to be
    negligible in mammals and birds who ingest the water. Concentrations of carbon
    tetrachloride and chloroform in game animals and game birds as a result of
    drinking water from Clover creek or Pugh Creek would be de minimis.
    As noted, carbon tetrachloride and chloroform are the main contaminants
    presently expected to migrate in high concentrations into the creeks. The
    potential Clover Creek concentrations at the years 1995, 2000 and 2010 are
    summarized in Table 6.
    To evaluate potential inhalation exposure of fisherman to chemicals in the
    Creek, an estimated air concentration at the air water interface was estimated
    by applying the same air/water partition constant (-PR-) as was used to
    evaluate the shower/bath exposure scenario for household use (see the RI,
    Section 6). Applying the PR of 1.3 to the highest water concentration of
    carbon tetrachloride predicted in Clover Creek of 1.164 mg/L, the estimated air
    concentration would be 1.5 mg/L. Assuming an immediate air dilution factor of
    10 at the creek surface and an additional 10-fold dilution due to mixing from
    the water surface zone to the breathing zone, the inhaled concentration would
    be 0.015 mg/~~'
    This would be in the general range of odor detection and approximately 50% of
    the time weighted average (-TWA-) for an acceptable level in the workplace.
    considering that the water concentration is based on the 3Q20 (low flow)
    estimate, that a fisherman would be exposed to the air on a contaminated area
    of the Creek only a few days per year, and that any wind velocity would greatly
    diminish exposure levels beyond the 100-fold aS8umption, the estimated
    potential air levels and related exposure levels are conservatively high and
    are not a health concern.
    Toxicitv Asse8sment
    The toxicity asse8sment presents" available human health and environmental
    criteria based on pertinent standards, advisories and guidelines developed for
    the protection of human health and the environment. An explanation of how
    these values were derived and how they should be applied is presented below.
    Cancer potency factor. (WCPFSW) have been developed by EPA's Carcinogenic
    Assessment Group for estimating exce.s lifetime cancer risks associated with
    exposure to potentially carcinogenic chemicals. CPFs, which are expressed in
    units of (mg/kg/day)-l, are multiplied by the e.timated intake of a potential
    carcinogen, in mg/kg/day, to provide an upper-bound estimate of the exceS8
    lifetime cancer risk a..ociated with exposure at that intake level. The term
    .upper-bound. reflect. the conservative estimate of the risk. calculated from
    the CPF. Use of this approach makes underestimation of the actual cancer risk
    highly unlikely. Cancer potency factors are derived from the re.ult8 of human
    epidemiological studies or chronic animal bjoas.ays to which animal-to-human
    extrapolation has been applied.
    Reference dose8 (-RfDS-) have been developed by EPA for indicating the
    potential for adverse health ettect. from expo.ure to chemicals exhibiting
    noncarcinogenic eftect.. RfD., which are expre..ed in unit. ot mg/kg/day, are
    e.timate. ot litetime daily exposure level. tor human., including .ensitive
    individuals.
    ~
    

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    - -
    5 9
    0040
    TAB LE 6
    ESTIMATED CLOVER CREEK CHEMISTR Y (mg/U
    fUT1JRE MODELED CONDITIONS
    HARDEMAN COUNTY LANDFILL RUFS
    Year Cuban Tetrachloride  Chloroform 
     3Q20 (l) Overall (2) Ann\U1 (3) 3Q20 (l) Overall (2) Annual (3)
     Low Average Average Low Average Average
     Flow Flow Flow Flow Flow Flow
    :995 1.164 0.069 0.088 0.238 0.01~ 0.013
    :000 1.000 0.059 O.OiS 0.182 0.011 O.Ol-y
    2010 0.549 0.033 0.041 0.082 0.005 0.006
    ~otes:
    " : )
    Lowest average daily flow over a 3 day period during 20 years.
    (:!)
    Annual average daily flow calculated from 17 measurements from 1980
    through 1987.
    ':3)
    Average daily flow based on the average annual flow from 1980 through 198:-
    ..
    

    -------
    -33-
    5
    9
    0041
    Estimated intakes of chemicals from environmental media (e.g., the amount of a
    chemical ingested from contaminated drinking water) can be compared to the
    RfD. The ratio of dose over RfD gives the hazard index ("HI"). Values of HI
    greater than l indicate an unacceptable exposure. RfDs are derived from human
    epidemiological studies or animal studies to which uncertainty factors have
    been applied (e.g., to account for the use of animal data to predict the
    effects on humans). These uncertainty factors help ensure that the RfDs will
    not underestimate the potential for adverse noncarcinogenic effects to occur.
    In evaluating the hazard from the non-carcinogenic effects of chemicals, the
    average daily exposure was based on potential shorter term (non-lifetime)
    exposure estimates, generally the average daily exposure for a year. To
    maintain a conservative approach, if the average daily exposure was
    significantly greater for a young child than for an adult (shower/bath and
    sWimming), the child's exposure was used to estimate the potential hazard.
    The RfDs used to calculate the hazard indices are presented in Table 7. These
    RfD values are taken from the Integrated Risk Assessment Information system
    ("IRIS") data base, if available from that source, or from the Health Effects
    Assessment Summary Tables ("BEAST"). No reference values were found for endrin
    ketone and endrin aldehyde, therefore the values for endrin are applied as
    surrogate values. The RfD value for di-n-butyl phthalate is applied to
    di-n-octyl phthalate as a surrogate value. These surrogate substitutions
    should result in conservative evaluations based on structure-activity
    relationships.
    In evaluating the hazard from the carcinogenic effects, the average daily
    exposure is based on lifetime exposure estimates. Lifetime estimated average
    .exposure levels are based on exposure for 10, 30, or 70 years of a 70-year
    lifetime. To maintain a conservative approach in each case, 6 years are
    considered to be childhood years and the daily dose for those 6 years were
    based on assumptions for a child's weight and exposure to estimate the
    potential additional lifetime cancer risk.
    The CPFs used to calculate the additional lifetime cancer risks are presented
    in Table 7. These CPF values are taken from the IRIS database, if available
    from that source, or from BEAST.
    water quality standards, criteria and advisories are also presented in Table 7
    for comparison with the reported concentrations in groundwater and surface
    water.
    Absorption efficiency of individual chemicals i8 not applied in the asse8sments
    of water exposure. orally ingested and inhaled doses are assumed to have 100\
    absorption. For dermal absorption, the permeability constant for water is used
    to determine water absorptions and the chemicals are assumed to be absorbed
    with the water in a proportional manner based on the reported concentration.
    The toxicity and chemical information for the contaminants of concern which was
    applied in this assessment is summarized in Table 7.
    Risk Characterization
    Excess lifetime cancer risks are determined by multiplying the intake level
    ~
    

    -------
    ,f'
    \D
                  CJ
                  C~I
                  -+-
         T AilE 7       I"I\~ I 01 2 1'0
       SUMMARY OF TOXICOI.OCY ANU O'EMJ '"KILKIJ 
    ,              
    Acrtu.w <;818 27U )'J4'J'i41 ~ 24 221:tllU 1111',/11 NA I III; III   ,It_I' 
    ,.,beN> Telr.,hl...KW IS) 84 117 HIli 281 I 11'.112 1'11..111 I 1/ HI 7111. H4 I.VI'I '" ),1111 Y 1111.' 
    (hionUnLf.."W 112S6 2b 4t111 HI4 1 11'.112 1 fN; .111 NA 2 III. 112 II\in '" hllltY 11111 
    ( hlufU'O.1n 119 J8 ]4~ 71111 191 ) I bill 2 'I': .111 h II 411 I II'. III In",-,  IHIII 
    Mdhyk". ( 101,,,..J,- 84 9) '>11 1'J7tU I II) HilI' .,1' ,111- ,III 1 (Jt. 411 b III II! 11\0\'1  !111M 
    1t't'luhlUftlt'lhylcM I to'> 9) l4 41\'> 1 till  ) bl'tll] 1 fI- 1111 tji\ I III. III I. VI f   
    ,.4..."", 9114 Jl '>ltI 17 1 (N; .lIl 111.1111 Ni\ 1111. III    
    Jlyl"11C C '..ull lOb lto 1(1 1'11\ 11 241:.11]   Ni\ !III: II_I    
    11,..42 ,"I.ylh...yllph'h"~IC )'J() '>7 h lI' ,III II WI .. II ,HI .lIi   I ~I II' !III II' 1111. I  1111,' 
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    /1/1. )'>4 4'J 711- 417 11,1" b2     141 III '> ,>,. 114    
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    f...Jro" AI.J~hy~ 01 31111119 2 Ilf 117 II 2b ) IS 7 21' ,112   NA 1 III. H4    
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    IIr.....h&... Ff'u...Jr J8'1]2 2 bl: jib U}'i '> 411     'I It ,II) I II- (/'i    
    

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    0"..;. .,
    ,
    At "tunr
    Co.h", 1t......I,I",""r
    ( hi...........,......
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    1'".I.."k...."", '11
    I:......i" Aldeh,.", 1.11
    II....... hi...
    Nu4.~.
    en
    '0
          UltE 7        I'."r 1... 1  
                    C) 
        WATER STANUAIIOS ANU (JlITERIA        C' 
        IIAIIUEMAN COUNn lANUI'II.L IIiit'S        +.:.. 
          '-.Ill         
                   '''''''I'S'' <..N 
      W.,,. U-.'ify ('.iI.... '''.'11 _..!~~~~..." 1/,."10 ,U..i,.,., !~!~-- ,,..,,  H,,"' '"K  
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     w'U O~"  b ri..  0.''1 "', IDa,  'OAIC 1Daj( IU, Hhi  ~,....J"fJ  
    7111       Nil Nil Nil Nil Nil  NA   
     ~ 11'00111' IIln'42 11111" IIn"'I4 4 III" 111111 Ill'> Nil 1/1. 1_. II'A  
    "I'  U4W U41111  Nil Nil Nil Nil Nil  riA MI I,  
     "I' II...." IIInll9 II I UII 'I  11111\1 Nfl NI' NI' Nil Nil I II- III   
      11.1111'1 IIlnll'l 11111'" III  I; H; 10 NA ) II. II/ Wt}....  
    Ilfl';  IIlnlllll II IU... IIln'lI 1  1 I ~  IIII'll!  rI,\   
    11111   I:; 14 ) 414 !II  , I III '"I. .UI  NA   
    ..nl'       411  .111 .UI "" III  tlA   
    14   I'»  > -.., Nfl Nil Nil NIl Nil I III. II/   
       ..  '4 1~4 Nil Nil Nil Nil Nil  NA   
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     1111'1 11"..11 II nil  111111  11111 II II!  tlUIl 11111 u..t!  NA   v.
         1
                  NA   
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    111.l1.li14  I II, II:; 1111: III 1 'It: III 11111 11111 III'" 111111> Nil 111.111   
    MUI. WT = .........Lo. Wr,sh'
    nom III/JUC = Mill;li/no Mr......., r.nou....,:II1 1)'11"""0 (."kiuo
    Soolut>iti'r: Soolul>di(r in w.lr. ., )() 11rs'ft"0 C "".uo
    1"11 kow = 11.ri,hm I........ III ulllw Ot.""uIlW~'", ..."... rquiliIM,um
    k... = W.1n /("........ «_""".1101\ ..1'" wlwn. .,bun ..... ..~..,. .1 '"'tuhbllum
    ecl' = lIouo:onr-II..ion ."'... loom ".Ift tuli.h
    (.W = e 8MWI P_, l''''kM..1w> I~.med (........ SIt'l'" F"."..I. ............ o"lio,,,.1 ......10:1 loom ........1 oJ.l.
    1110 = ............doH cw d.- nul ...pe"'" lu ........ 8
    -------
    r
    "
    '-'
    9
    n 0 ' ~
    U '-tLf
    -36-
    wlth the cancer potency factor. These risks are probabilities that are
    generally expressed in scientific notation (e.g., 1x10-6 or 1E-6). An excess
    lifetlme cancer risk of 1X10-6 indicates that, as a plausible upper bound, an
    lndlvldual has a one in one mlllion chance of developing cancer as a result of
    slte-related exposure to a carclnogen over a 70-year llfetime under the
    speclfic exposure conditions at a site. The Agency considers indivldua1 excess
    cancer rlsks ln the range of 10-4 to 10 -6 as protective.
    Potentlal concern for noncarcinogenic effects of a single contaminant in a
    slng1e medium is expressed as the hazard quotient ("BQ") (or the ratio of the
    estlmated intake derived from the contaminant concentration in a given medium
    to the contaminant's reference dose). By adding the HQs for all contaminants
    withln a medium or across all media to which a given population may reasonably
    be exposed, the Hazard Index ("HI") can be generated. The BI provides a useful
    reference point for gauging the potential significance of multiple contaminant
    exposures within a single medium or across media.
    Estimated total incremental lifetime cancer risk from future household use of
    groundwater using present conditions was calculated for wells GH-S, 13 and
    GHP-5. These wells are located on the appro~imate center line of the
    downgradient plume and are positioned between the northern boundary of the
    disposal area and the edge of Pugh and clover creeks.
    The risk and hazards from individual chemicals show that the calculated risks
    and hazards are related primarily to the presence of carbon tetrachloride which
    accounts for over 90\ of the total risk and hazard at each well.
    The chemicals of concern at the site are primarily liver toxicants and as such
    it is appropriate to sum the incremental risks and hazards for the several
    primary chemicals reported in groundwater. since the exposures would all
    relate to the local population, it is also appropriate to sum the risks from
    the two household uses of groundwater, namely drinking and bathing. The total
    incremental risks and hazard presented by household use of the groundwater are
    summarized in Table 8 based on level 1 assumptions (see page 26). It is
    apparent that the risks and hazards all exceed acceptable levels by several
    orders of magnitude. This is to be expected since the reported concentrations
    exceed Water Quality criteria for drinking water by several orders of magnitude
    and the Health Advisories for drinking water by 2 to 3 orders of magnitude.
    The additional lifetim8 risk of cancer and the non-carcinogenic hazard from
    exposure to surface waters of the creeks based on the site-specific indicator
    chemlcals are 8ummarized in Table 9.
    In the 8ingle instance where the assessment shows unacceptable risk from
    surface water (eating fish from Pugh creek, P3a), the risk is almo8t totally
    from the reported level of PCBs which is probably not originating from the
    site. As discussed earlier, the reported concentrations of pesticides, PCBs
    and phthalates are apparently from background sources or are analytical
    artifacts, and are not considered to be Site-related. The reported
    concentrations of organic solvents in the ROund 2 creek samples co~ld
    rea80nably be Site-related although the upstream sample from location C2a has
    the highest concentration of carbon tetrachloride reported in clover Creek.
    ...
    

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    -37-
    5
    9
    0045
    TABLE 8
    St.iMMARY OF CA~CER RISK A~D HAZARD [~DEX
    AVERAGE EXPOSL"RE SCE~ARIO ill
    GROt:~DWATER I="i DOW~GRAQ[E~'" PlL~E
    HARDE~A.\l COt:~'TY LA~DFILL RL'FS
      Cancer Risk Ha:ard [ndn
    Well I.D. Round I Round 2 Round I Round 2
    On-Site Average 1.4E.ol 1.1E+OO UE+04 1.1E.OS
    C\o1-S 4.2E.ol 1.8E+OO 4.4E+04 1.9E.OS
    1~ 3.9E.ol 7.7E-ol 4.1E+04 1.:!.E+OS
    CMP-S 3.3E.ol 4.7E.ol 3.SE+04 4.9E+04
    (1)
    Average exposure scenario is the Level 1 scenario for future
    household use fran current carbon tetrachloride and chloroform
    levels in grourdwater
    ,.
    

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    -3.3-
    5 9
    0046
    TABLE 9
    SUMMARY OF CANCER RISK AND HAZARD INDEX
    AVERAGE EXPOSURE SCENARIO (1)
    PRESENT REPORTED CONCENTRATIONS
    SURFACE WATER IN CLOVER AND PUGH CREEKS
    HARDEMAN LANDFILL SITE RifFS
    Welll.D.
    Cancer Risk
    Round 1 Round 2
    Hazard Index
    Round 1 Round 2
    Clcn'er Creek
    C2a Cpstream
    C2 Upstream
    C3b
    C4
    O.OE+OO
    1.4E-06
    O.OE+OO
    4.0E-05
    1.3E-07
    4.7E-08
    ~A
    8.1 E-08
    9.5E-02
    3.9E-02
    3.2E-05
    3.8E+00
    1.4E-02
    5.1 E-03
    NA
    8.9E-03
    Pugh Creek    
    P2a Upstream 7.0E-08 NA 1. 9E-01 NA
    P2b Upstream O.OE+OO NA 1.9E-01 ~A
    P3a 3.3E-03 NA 5.6E-01 NA
    P4 1.4E-07 1.6E.07 2.1E-01 1.7E-02
    P5 3.3E-07 6.5E-06 3.6E-01 4.2£-01
    P6 O.OE+OO \lA 9.5£-02 \!A
    ;..; otes:
    ~ A - Not Analyzed
    (1) A verage Exposure Scenario is the Levell Scenario
    ....
    

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    1
    0047
    -39-
    Assuming the carbon tetrachloride is Site-related, examination of the risk and
    hazard assessment results show that the reported concentrations do not present
    a concern for fish consumption or for occasional skin contact. The swimming
    exposure component of the assessment calculations would greatly exceed any
    casual skin exposure component related to wading or fishing.
    Based on the results of the risk calculations, it is evident that the potential
    exposure to volatile compounds in the air due to specific chemicals
    volatilizing from the surface waters while fishing does not represent a
    significant risk to the general public.
    By the application of appropriate modeling techniques, water concentrations of
    carbon tetrachloride and chloroform were predicted in the wells downgradient of
    the landfill and in the creeks. Values predicted for the years 1995, 2000 and
    2020 in Wells GM-5, 13, 7, and GMP-5 were evaluated for potential total
    incremental lifetime cancer risk and non-carcinogenic hazard using the same
    household exposure or recreation scenarios as were used for evaluation of
    present conditions. The summary data are presented in Tables 10 (groundwater)
    and 11 (surface water).
    .
    Upon examination of. Table 10, it is apparent that the estimated risks and
    hazards are still far in excess of acceptable levels, even in the year 2010
    after an additional 20 years of migration of the plume without further
    remediation.
    The predicted concentrations of carbon tetrachloride and chloroform in clover
    Creek are estimated to peak in the year 1994. Table 11 shows a gradual
    decrease of estimated potential risk and hazard after the year 1995. At the
    estimated period of peak flux to the creek between the years of 1993 and 1995,
    estimated potential risks are below the target range of 1E-04 to 1E-06
    estimated total incremental lifetime risk of cancer. The estimated total
    hazard level is also below a level of concern even applying the more
    conservative conditions of 3Q20 creek flow where the estimated groundwater flux
    from the plume area makes up approximately one-half of the total creek flow.
    Uncertainties
    Regardless of the type of risk estimate developed, it should be emphasized that
    all estimates of risk are based upon numerous assumptions and uncertainties.
    In addition to limitation. associated with Site-specific chemical data, other
    assumption. and uncertainties that affect the accuracy of the Site-specific
    risk characterizations result from the extrapolation of potential adverse human
    health eff.ct. from animal studies, the extrapolation of effects observed at
    high-dose to low-dose effects, the modeling of dose response effects, and
    route-to-route extrapolation.
    The use of acceptable levels (established standards, criteria and guidelines)
    and unit cancer risk values which are derived from animal studies introduces
    uncertainty ,into the risk estimate.. In addition, the exposure assumptions
    used in estimating individual dose levels are often surrounded by
    uncertainties. As such, the.e estimates should not stand alone from the
    various assumptions and uncertainties upon which they are ba.ed. In developing
    numerical indices of risk, an attempt i. made to evaluate the .ffect of the
    a.sumptions ,and limitation. on the numerical ..timat...
    ~
    

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    We/ll.D.
    C\-1-5
    CMP-5
    (1 )
    -_.1-
    5
    9
    0048
    TABLE 10
    SL'MMARY OF CASCER RISK A:-';D HAZARD ISDEX
    F1.rn.:RE ESTI~A TED CO:-';CE:\'TRA TIO:-.;S
    GROL"NDWATER IN DOWNGRADIE:-';T PLL~E
    HARDE~AN U.:-';DFILL SITE RI/FS
    13
    Cancer Risk (1)  Ha:ard Index 
    2995 2000 1020 1995 1000 2.010.
    1. :""E.OO 1.0E.00 -4.:2£-01 1.8E.05 1.1:: ...05 .UE...V4
    l.4E.OO 8.9E-01 3.7E-01 UE.05 9.3E.04 3.8E.04
    1.1E...00 9.0E-01 4.:£-01 1.1E...05 9.4E.04 4.4E...04
    8.4E-01 7.7E-01 3.9E-01 8.9E.04 8.0E.04 4.1E.04
    Risk estimates presented for the average (level 1) scenario for
    groundwater exposure fran dri.nk~ and bathing exposure to
    carbon tetrachloride and chloroform
    ,.
    

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    -"'..-
    5
    9
    0049
    TABLE 11
    StiM.'-fARY OF CA='iCER RISK A~D HAZARD {;...1)EX
    Ft.JTt"RE EST1~ATED CO~CE~TRAT10~S
    St"RFACE WATER I~ CLOVER CREEK
    HARDE~A~ LA~DFlLL SITE RI/FS
     Cancer Risk!I)  Ha:ard Index(2)
    Welll.D. 2995 2000 2020 1995 2000 2020
    Carbon Tetrachlonde 3.iE.Q7 3.~E.Q7 1.8E-07 6.9E.Q1 5.9E.Q1 3.2E.Ql
    Chloroform 1.5E.Q9 1.2E.Q9 5.5E-10 5.9E.Q3 ~.5E.Q3 2.0E.Q3
    T 01315 3.7E.Q7 3.2E.Q7 1.3E.07 6.9E-01 5.9E.Ql 3.3E.{)1
    (1 )
    ~dative cancer risk. based on level 1 exposure assumptions
    for all relevent pathways
    (2)
    Hazard i.n:iex based on "3Q20" estimates
    . .
    . '.
    

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    9
    ("'\ ,', c 0
    uu"
    -42-
    7he uncertainty factors which are incorporated into the risK estimates are
    bel~eved to be conservative. As such, when they are considered collectively,
    exposure and subsequently risK may be overestimated. On the other hand, these
    es~~mated risk calculations were based on present conditions at the Site,
    ~ncluding the cap, and no maJor ~ncreases of contaminants already in the
    aqu~fer. Additional risK could occur should the concentrations increase or the
    cap erode.
    In conclusion, based on the results of the risk assessment, actual or
    threatened releases of hazardous substances from Site, if not addressed by
    ~mplementing the response action selected in this ROD, may present an imminent
    and substantial endangerment to public health, welfare, or the environment.
    Environmental RisKS
    As previously stated in this ROD, the final potential environmental risks
    associated with the site will be addressed as part of the second operable unit.
    Previous studies have generally indicated that the contaminants migrating from
    the Site are not presenting an environmental risk since the contaminants are
    highly volatile and do not concentrate or bioaccumulate in the environment.
    However, additional studies concerning these waste. and the more persistent
    compounds located in the di~posal areas are required for a final analysis.
    Also, although previous investigations have not identified any endangered
    species in the area of the site, it has recently been determined, and will have
    to be verified, that an endangered species of bat may exist in the vicinity of
    the site.
    DESCRIPTION OF ALTERNATIVES
    The surficial aquifer is under consideration for remediation due to the
    .unacceptable risk associated with the con8umption of the contaminated
    groundwater.
    Based on the contamination detected in the aquifer at different locations, the
    groundwater has been divided into two areas: on-site and off-site. The on-site
    groundwater i8 that portion of the aquifer located directly beneath the
    disposal areas. The off-.ite groundwater is that portion of the aquifer
    located beneath all properties surrounding the dispo.al areas. The off-site
    groundwater contains mainly the highly mobile contaminant. like carbon
    tetrachloride and chloroform. The following is a list of the remedial
    alternative. under con.ideration for the contaminated groundwater. The FS
    Report contain. a more detailed evaluation of each alternative.
    1 )
    No action (A1 and B1 in the FS).
    2 )
    On-site Groundwater Extraction through well., Treatment, and surface
    Water Discharge (A4 in the FS).
    3 )
    In.titutional Control. (B2 in the FS).
    4 )
    Off-site Groundwater Extraction through well. and a collection
    trench along pugh and Clover creek., Treatment and Surface Water
    Di.charge (B4in FS).
    ..
    

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    5
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    ,..,-.r-1
    UU;)
    -43-
    5 )
    Off-site Groundwater Extraction through a' collection trench along
    Pugh and Clover creeks, Treatment anet surface Water Discharge (86 in
    FS) .
    6 )
    Off-site Groundwater Extraction through wells, Treatment, and
    Surface Water Discharge (88 in FS).
    It should be noted that groundwater reinjection was considered in the FS for
    each of the groundwater ,treatment remedies. However, groundwater reinjection
    is' not considered feasible due to concerns over the ability of the aquifer to
    accept all of the reinjected water, the affects of the reintroduced water on
    contaminant flow, and the long-term maintenance of the injection wells, which
    may plug up over time due to mineral precipitation.
    All of these alternatives except -No Action- involve restrictions on land:and
    well use in the vicinity of the site, upkeep of the fence arid property, and
    monitoring to assess the effectiveness of the' remedy. Each alternative also
    includes identifying and evaluating possible additional remedial actions
    required for addr~ssing the contamination of the entire Site including the
    contaminant source (the disposal areas) and posslble environmental/ecological
    concerns.
    ALTERNATIVE 1: NO ACTION
    pre.ent Worth (PW) cost $0.00
    Years to Implement: 0
    CERCLA requires that the -No Action- alternative be considered at every site.
    Under this alternative, no groundwater containment or treatment would take
    place. The only reduction of contaminant levels would occur via natural
    processes such as dispersion and attenuation. since moni1;oring' is already part
    of the disposal areas maintenance, additional cost would not be incurred.
    ALTERNATIVE 2: ON-SITE GROUNDWATER EXTRACTION. TREATMENT AND SURl"ACE
    WATER DISCHARGE
    Present Worth Cost: $7,266,000
    PW capital cost: 3,146,500
    PW O'H Cost: 4,120,000/30 yr.
    Years to Impl8JD8nta 2
    Alternative 2 provides for tbe hydraulic containment of the contaminated
    on-site groundwater along tbe nortbern boundary of tbe disposal areas. ,
    Approximately 5 extraction vells would be installed to,develop a bydraulic
    gradient along tbis northern boundary line preventing on-site groundwater
    contamination above HCLs fraa leaving tbe dis~sal areas. Extracted on-site
    groundwater would be pumped to a treatment system located on the site property
    for treatment of groundwater to National pollutant Discbarge Elimination Syst..
    C-NPDES8) concentrations establisbed as part of the clean Water Act for surface
    water discharges. The contamination, particularly carbon tetrachloride,
    chloroform, and naturally occuring matals, would be treated using settling
    tanka for solids removal, air stripping and carbon adsorption. Treated
    ,.
    

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    -44-
    on-site groundwater would be di~charged to one of the nearby surface water
    bodies (Pugh or clover Creek) and would comply w~th NPDES discharge
    requirements.
    ALTERNATIVE 3: INSTITUTIONAL CONTROLS
    Present worth Cost: $1,088.00
    PW capital Cost: 60,000
    PW O&M Cost: 1,028,000/30 yrs.
    Years to Implement: 50
    Alternative 3 provides only for the restrictions of land and groundwater use In
    the contaminated areas. It includes the monitoring of the contaminat~on and
    its migration off-site. Reduction of contaminants to acceptable levels would
    occur only through natural processes and will require an estimated 50 years
    before cleanup goals would be met.
    ALTERNATIVE 4: OFF-SITE GROUNDWATER EXTRACT:ON THROUGH WELLS AND A COLLECTION
    TRENCH ALONG PUGH AND CLOVER CREEKS. TREATMENT AND SURFACE WATER DISCHARGE
    Present worth Cost: $11,791,500
    PW capital Cost: 6,568.500
    PW O&M Cost: 5,223,000/30 yrs.
    Years to Implement: 2
    Alternative 4 addresses the containment and recovery along Clover creek and the
    extraction of off-site groundwater in the areas of highest contaminat~on. A
    slurry wall and collection tile system would be placed along clover creek
    station at the confluence of clover creek and pugh creek for approximately
    8,000 feet (see Figure 16) to the western limit of the plume to collect
    contamination already entering the creeks.
    Approximately 10 extraction wells would be installed into the high
    concentration areas of the off-site groundwater to control further migratlc~ cf
    the plume toward the creeks and to treat the groundwater to MCL concentra~lon
    levels. The extracted water would be pumped to an off-site system for
    treatment. The system would consist of settling tanks, air stripping and
    carbon absorption. Treated groundwater would be discharged to one of the
    nearby surface water bodies and would comply with NPDES discharge requ~rements.
    ALTERNATIVE 51 OrF-SITE GROUNDWATER EXTRACTION THROUGH A COLLECTION TRENCH
    ALONG PUGH ~ CLOVER CREEKS, TREATMENT AND SURFACE WATER DISCHARGE
    Present worth cost: $9,384,000
    PW capital Cost: 4,727,000
    PW O&M Costs: 4,657,000/30 yrs.
    Years to Implement: 2
    Alternative 5, like Alternative 4, addresses the containment and recovery ~~
    off-site contaminated groundwater along clover Creek. A slurry wall and
    collection tile system would be placed along Clover creek; however, no
    

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    LEGEND
    ----
    APPROXIWA TE: UW'TS OF PLUWE
    COI.J.£CT1ON DRAIN AUGNWENT
    ~: . :..;. .:
    CJ:..:.::.:-:-:'. :.~:'.
    "
    

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    5
    9
    f"\u~rl.
    u. :) {~
    -46 -
    extraction wells would be installed in the high concentration areas of the
    groundwater plume, The contaminated groundwater would be treated and.
    discharged in the same manner described in Alternative 4,
    ALTERNATIVE 6: OFF-SITE GROUNDWATER EXTRACTION THROUGH WELLS. TREATMENT AND
    SURFACE WATER DISCHARGE
    Present worth Cost: $4,378,000
    PW capital Cost: 1,936,000
    PW O&M Cost: 2,442,000/30 yrs,
    Years to Implement: 2
    Alternative 6 provides for the removal of contaminated off-site groundwater
    from the plume in the areas of highest concentration. Approximately 10 wells
    would be installed into the high concentration areas of the off-site plume to
    control the groundwater contaminant migration and remediate the off-site
    groundwater to MCL concentration levels. The off-site groundwater treatment
    and discharge would be the same as Alternative 4 and would comply with NPDES
    requirements.
    ~
    Any remedy implemented for OP unit t1 shall meet the performance standards set
    forth below which are the Applicable or Relevant and Appropriate Requirements
    ("ARARS") identified for these remedial alternatives.
    Remediation of contaminated groundwater for a Class IIa aquifer is required to
    meet MCLs as established under the Safe Drinking Water Act (40 CFR 141, 143)
    and, if possible, to attain Maximum contaminant Level Goals ("HCLGs"). HCLGs
    can not be enforced as cleanup levels since they are sometimes technically
    impossible to meet; however, groundwater sampling will monitor for HCLGs as a
    possible result of the groundwater extraction and treatment. The groundwater
    remediation levels for the contaminants of concern in the aquifer are
    identified in Table 12. Reduction of the contaminants to the8e levels will
    reduce the risk posed from the consumption of contaminated water from an
    absolute risk over a ten year period to a risk of 8.2 X 10-sfor a 70 kg adult
    over a iifetime (70 year.). Thi. ri8k falls within EPA's acceptable risk range
    of 10-4to 10-6.
    Any discharge to a nearby .urface water body is required to meet NPDES
    standards e.tablished by the clean Water Act and regulated by the State of
    Tennessee. Pugh and Clover creeks are classified for fish and aquatic life,
    recreation, irrigation, live.tock watering and wildlife. The allowable
    in-stream contaminant levels based on State and Federal regulations are
    identified in Table 13. Final discharge levels will be determined by surface
    water flow information, contaminant levels, and biological testing that will be
    established by the state of Tennessee. The surface water discharge will be
    required to meet the NPDES limit8 that are e.tabli.hed.
    since contaminants are presently still leaching from the disposal areas, a
    Point of compliance, as defined under regulation. promulgated pur.uant to the
    Re.ource con.ervation. and Recovery Act ("RCRA") (40 CrR section 264.95) i8
    relevant and appropriate for determining the point or line on the site beyond
    which contaminant level8 in the groundwater must be remediated to HCL8. The
    ..
    

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    9
    0055
    '!'ABLE :2
    GROUNDWATER REME~:A'!':ON LE'JELS ~OR
    CONTAMINANTS OF CONCERN AT THE
    VELSICOL/HARDEMAN COUNTY NPL SITE
    CONTAMINANTS   GROUNDWATER   
    OF CONCERN   REMEDIATION LEVEL ( 1) MCLG(2) RISK(3)
        (mg/1)  (mg/1) 
    VOLATILE ORGANICS      
    Acetone   0.7 (4)  
    Carbon Tetrachoride   0.005  0.0 1. 9x10-S
    Ch1orobenzene   0.1  0.1 
    Chloroform   0.006 (5)  1. OxlO-6
    Methylene Chloride   0.005  0.0 1. lx10-6
    Tetrachloroethene   0.005  0.0 7.SxlO-6
    Toluene   1.0  1.0 
    Xylenes   10.0  10.0 
    ~       
    Bis (2-ethylhexyl) phthalate 0.004  0.0 1. 6x10-6
    Di-n-butyl phthalate  0.7 (4)  
    Di-n-octyl phthalate  0.14 (4)  
    2,4 - Dichlorophenol  0.1 "( 4)  
    PESTICIDES      
    Endrin   0.0002 (6) 0.0002 
    Endrin Aldehyde   0.0002 (6) 0.0002 
    Endrin Ketone   0.0002 (6) 0.0002 -
    Heptachlor   0.0004  0.0 5.2xlO-S
           --------
    TOTAL CARCINOGENIC RISK    a.2xlO-S
    (1) Maximum Contaminant Levels (MCLS) as promulgated under the Safe
    Drinking Water Act (40CFR 141,143) were used as the remediation
    level for all contaminants that have an MCL. Contaminants without
    MCLs are identified numbers, and the source of the remediation
    level is identified in the footnotes.
    (2) MCLG - Maximum COntaminant Level Goal. A non-enforceable
    concentration of a drinking water contaminant that is protective of
    adverse human health effects and allows an adequate margin of
    safety.
    (3) Ri8k is calculated for the carcinogenic compounds
    (4) Lifetim8 aealth Advisory (LHA). A lifetime exposure concentration
    protective of adverse, non-cancer health effects, that assumes a
    relative source contribution (RSC) of 20' of the contaminant in a
    drinking water source. (January 31, 1991, Federal Register, page
    3535.)
    (5) Level set for a lifetime risk (70 years) of 10-6 (one in one
    million exces. cancer risk level for drinking water).
    (6) On July 25, 1990, a MCL and MCLG of 0.002 mq/l was proposed but is
    not final for endrin. Should the MCL be made final, 0.002 mg/1
    will be the endrin remediation level. The other endrin compounds
    are based on the level set for endrin.
    .
    

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    9
    "0 r"" 6 
    U :J
    -:- .i.5~= J.:3
    PLAMNING LIM!TS-:~S7R~A~
    VELISCOL CHE~!CAL au~~, ~AR:E~A~ CCUNTY
    The following instream limits are orov~ded for planning
    pu~~oses and are valid for one year. Ary limits to be
    included in a discharge per~i~ ar~ sJcje~~ to t~e ~~b:i~
    ~o~ice ~rocess, t~e exact locatio~ of t~e disc~arge and t~e
    relative size of the discharge.
    Compounds
    VO~ATIL.~S
    Acetone
    Benzene
    Carbon disulfide
    Car~on tetrach: o~ ~ :~.
    Chlorobenzene
    Chloroform
    Methylene chlorice
    Tetracnloroet~er.e
    Toluene
    Tr-ichloroethene
    Xylenes
    Bis(2-ethylexyl)ph~~a1ate
    Di-n-butyl phtha~ate
    Di-n-octyl phthala~e
    2/4-Dichlor-opheno~
    Naphthalene
    Dieldrin
    Endr-in
    Endr-in Aldehyde
    Endr-in Ketone
    Heptachlor
    Aluminum
    Arsenic
    Barium
    Cadmium
    Calcium
    Chromium VI
    Total
    B~As
    P~ST!CIDES
    "'E~AL.S
    Copper
    Iron
    Lead
    Magnesium
    Manglnese
    Mercury
    Nickel
    Potassium
    Selenium
    Silver
    Sodium
    Zinc
    ... Technology based limit ap~lies
    ~ ':J ~ ~e
    ,
    :~st;ea~ limi~, ~g/L.
    (chr"onic/a~u~e)
    0.CC5*
    0.005/C.044
    47.0
    16.0
    0.088
    0.010*
    0.005/0.807
    0.010.
    0.059
    ~ 2 . 0
    - 6 .
    1.9x10 /0.0025
    2.3)('0-6/0.000~8
    -
    
    2.0x~O-6
    0.087/0.75
    0.19/C.36
    0.0007/0.002
    0.0"/0.O~6
    0.01 chr-onic
    0.007/0.009
    1.0/2.0
    0.001/0.034
    -
    
    1.2x10-5/0.0024
    0.088/0.79
    0.005/0.020
    0.001 acute
    0.059/0.065
    discharge.
    

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    -49-
    OuS7
    Point of compliance ("PCC") for this ROD is established by identifying the
    disposal areas and setting the POC at the edge of these areas as shown ~n
    Figure 17. Due to the steep relief along the edge of the disposal areas at
    th~s site especially along the northern and eastern sides, the POC is set at
    the base of the grade of the disposal areas.
    Land Disposal Restr~ctions ("LDRs") as set forth in regulations promulgated
    pursuant to RCRA (40 CFR Part 268) may be applicable to the residuals of the
    groundwater treatment facility, spec~fically the sludge from the settling tanks
    wh~ch may requ~re RCRA disposal. spent carbon from the treatment process
    should be able to be regenerated for additional use.
    The Clean Air Act is an ARAR for the releases to air from the air stripper.
    Releases from the stripper will comply with Federal and State Clean A~r
    Standards.
    Any work performed in the area of Clover Creek could affect the wetlands along
    Clover creek, and 40 CFR Part 6, Appendix A concerning responses in a wetlands
    would apply.
    SUMMARY OF COMPARATIVE ANALYSIS OF ALTERNATIVES
    The remedial alternatives developed during the site FS were evaluated by USEPA
    u8ing the followi~g nine criteria. The advantage. and di.advantages of each
    alternative were' then compared to identify the alternative providing the best
    balance Among the.e nine criteria.
    1.
    overall protection of Human Health and the Environment addresses
    whether or not an alternative provide. adequate protection and
    describes how risks are eliminated, reduced or controlled through
    treatment and engineering or institutional controls.
    2.
    Compliance with Applicable or Relevant and Appropriate Requirements
    (ARAR.) addre8ses whether or not an alternative will meet all of the
    applicable or relevant and appropriate requirement. or provide
    ground. for invoking a waiver.
    3.
    Long-term Effectivene..
    alternative to maintain
    environment, over time,
    ability of an
    health and the
    been met.
    and Permanence refer. to the
    reliable protection of human
    once cleanup objective. have
    4.
    Reduction of Toxicity, Mobility or volume i. the anticipated
    performance of the treatment technologies an alternative may employ.
    5.
    Short-term Effectivene.. involve. the period of time needed to
    achieve protection and any adver.e impact. on human health and the
    environment that may be po.ed during the con.truction and
    implementation period until cleanup objective. are achieved.
    6.
    Implementability i. the technical and admini.trative fea.ibility of
    an alternative, including the availability of good. and service.
    needed to implement the .olution.
    .
    

    -------
    .. DISPOSAL. AREAS
    . APPROXIW. T! L.OC. TlON
    OF I/ELSICOL DEE? 't\t:LL
    --- STUDY AREA
    -.- DISPOSAL. SITE
    a
    ?E~5:~NEL. SUPPORT z:~~
    _. _. - - .-
    ~. ..;~~ -
    ....... -
    Point of Compliance
    =':'i\-: '7" ~Y.?:":.:"'.
    ..
    

    -------
    5
    9
    - .
    (""'\ -, r ()
    LJU-J
    7.
    Cost lncludes capital costs, as well as operation and malntenance
    costs.
    8.
    Agency Acceptance lndicates whether, based on its review of the
    RIfFS and Proposed Plan, TORE agrees wlth USEPA on the preferred
    alternative.
    9.
    community Acceptance lndicates the publlc support of a given
    alternatlve. ThlS criterla is dlscussed in the Responslveness
    swnmary.
    Table 14 contains an evaluation and comparison of
    the groundwater using seven of the nine crlteria.
    Acceptance are discussed below.
    the six (6) alternatlves for
    State and communlty
    State Acceptance
    TOB!: has assisted USEPA in the review of reports and Site evaluations. TOBE
    has reviewed and concurs with the selected remedy for the groundwater (see
    Appendix B).
    Community Acceptance
    Community response to the alternatives is presented in the aesponsiveness
    summary (Appendix A) which addresses comments received during the public
    meeting and public comment period. Although the public had general questions
    concernlng the remedy, no comments were received that indicated the need for a
    major change in the remedy selected.
    SELECTED R1!:MEDY
    The selected remedy for the contaminated groundwater is a combination of
    Alternatives 2 and 6. This remedy involves the hydraulic containment of the
    on-site groundwater using extraction wells to prevent the on-site groundwater
    above HCLs from leaving the disposal areas and the extraction of cont&mlnated
    off-site groundwater to remediate the contaminated aquifer beyond the POC down
    to HCLs. After groundwater is extracted, it will be treated and then
    discharged to a nearby surface water body (Pugh or Clover creek).
    The selected remedy will include the following:
    i)
    Extraction wells (approxim£tely five (5») and pumping systems wlll
    be inltalled to achieve an effective hydraulic capture of
    contaminantl in on-lite groundwater at the POC (see Page 46).
    Approxim£te locationl of these extraction well. are .hown in Figure
    18; however, locations of these well. will change to comply with the
    POCo It i. e.tim£ted that the.e well. mu.t collectively recover
    approxim£tely 200 qpm to achieve hydraulic containment. Piezometers
    may be in.talled within the projected containment area to
    demonstrate capture.
    ii)
    Extraction well. (approxim£tely ten (10» and pumping IYlte~ will
    be in.talled to restore the contaminated off-.ite groundwater beyond
    the POC to within acceptable drinking water standards by removlng
    groundwater from the areas of peak contaminant concentratlon. :t
    ...
    

    -------
    TABLE 14:Evaluation o' Groundwater Remedial Alternatives
    (J1
    '-0
    Ev8lual1on C.U..1a
    AUe.f\8U..e 6
    AI18.nall". .
    AU..nal.... 2
    Alte.natlv. J
    AU..nal.... 4
    AU..naU... S
    0.... PmllIC1lUO of
    PutIIIc He8lh and Ih8
    Enwonmenl
    No ~.prov1d8d
    W. provide overa.
    protection of IU*:
    heaIh W. noI
    inunedI8IeIv fII'*a lhe
    -~ lrom .
    011. SoW CIft)Uf1dIIIt....
    oont8lllln8l1on
    W. pruvwte overal
    prot...,,,,,, of IU*:
    healh. .. noI prua1
    .he -1IOf1fn8f1I 'rom
    .,..........
    oonI_llOI1
    CGmpNnm ...h
    . ARAR'. 1St... and
    f...eI Reyu&aIIonaI
    0... noI CIDIItfJIr willi
    .... ........
    CompIi8a with ..
    8IIIJIic88II8 .... ....
    ...... ........ lor
    ..... JIIQUfII»""
    an"""'"
    W. pnNlI1B ""&laY
    prot""',on of puUoo;
    healh ....11he
    -- sp8I:''''''
    by lhe 0 P lJrwfs
    obfBd'ves
    . Same 85 Alemalove 4
    Sa,,,.. as AI"m8lhle 4
    o
    o
    0'\
    o
    ----__'__0______---..--- -..---- .
    s ."... as AI_- 4
    Doea noI ~ w8h
    .... .... .....11
    regulations 0IIn08fTW1U
    gmundIIo- ...,...
    lion.
    #
    Lang.- ~
    .... ..........
    0... noI .......
    0IIIIIMI8I8I8d QIIQUfId
    .....
    Lang.18Im ~
    of 01.", glUUflllw8181
    .. -**'W oa:ur
    - .. ....... of
    ~ II» 08.'"
    """'_1188 ......
    ....--...
    ~ ..-wIa IU*:
    ... of gIOUI1doI-
    Doea noI ~
    ........ oontamine.
    .ion
    CDmploes ..Ih al
    eppI8:.able slate -
    IedoNIi ~ lor
    IIIh... \IIOUf1dw-
    ronIllllin8lion
    Same as AIIen...",e 4
    . - ------. --.--.-
    . ---------'-----'-----'-- ------ -._-" ----- .--..-
    W. I8fJIOV8 ronI8ffII'
    nanls lrom 011-...
    JIfOUfIdw-. but dues
    noI 8dIhu anami.
    nanI ....... 110m Ihe
    ... May cauu
    ~ c:h8ngea in
    Ih8 WMI8ndI
    Reduction of foaUly,
    Ma8Ii8Iy. Of VoUne
    Redua8 gmundIIo-
    08.'" ID MCLI
    Doea ... ...... 01
    8IIIninIII8 .... hal81dDu8
    .....
    ...... gro&RIw-
    ~ INving
    .. ... ID UCla.
    S_u~l.
    W. f8f'ROV8 OOf1Iaml.
    R8fIIs prioo 10 them
    ..-.ng 'he t:I88II. but
    ~ noI lWn8dI8Ie Iha
    011.. gmundIIo-
    May cNng8 -18nds
    Remedl8loons oft. sae
    \IfOUIIdIoraner -"'1Iv
    r~~"ln9 (ont..l-
    nants .nt~rln9
    th~ (r~~'\.
    --~-, ------------------..
    S.'ne as AlemaalVe 4
    I
    L"
    ,~
    I
    Reduces oonIam",at"",
    ..-ing ... moeks
    ~ noI ......
    grourdoo- m
    -------
    5 9
    ~ '\ ". 1
    LJUo
    -53-
    ~
    -36Ci -
    ~
    

    -------
    vii)
    viii)
    7
    ~~U~
    -54-
    is estimated that these extraction wells will have a pumpinq rate of
    approximately 30 qpm each. Approximate locations of these
    extraction wells are shown in Figure 19; however, locations of these
    wells could chanqe based on movement of the contaminant plume.
    iii)
    Groundwater from all extraction wells will be pumped via a forcemain
    system to the treatment plant on the Site property as shown in
    Fiqure 19. It is estimated that approximately 8000 to 9000 lineal
    feet of forcemain will be required to connect all of the extraction
    wells and the treatment plant.
    iv)
    Contaminated qroundwater will be treated in the treatment plant
    usinq a system conceptually desiqned to consist of settlinq tanks
    for solids removal, air strippinq and final carbon adsorption
    treatment for off qas treatment and final qroundwater polishinq
    prior to discharqe. A conceptual desiqn of the system is shown
    schematically in Figure 20. It is estimated that the plant will be
    treatinq approximately 550 qpm of water contaminated with an
    approximate total Voc concentration of 15 mqlL. The treatment
    system will be required to comply with air emissions standards and
    NPDES requirements (see paqe 49) prior to surface water discharqe
    and may be modified to meet these requirements.
    V)
    Treated water will be discharqed to one of the nearby surface wate~
    bodi.s (Puqh or Clover creek) in compliance with NPDES requirements
    via a forcemain pipinq system.
    vi)
    Groundwater monitorinq will be conducted to determine the
    effectiveness of the qroundwater extraction and verify that
    qroundwater remediation qoals (Table 12) are reached for the
    off-site qroundwater beyond the POCo
    Deed restrictions, siqns, and institutional controls will be
    established to identify the presence, quantity and nature of wastes
    in the disposal area and qroundwater and limit uses of both until
    remediations are complete.
    Haintain the qroundwater treatment system and the disposal area.'
    cover. Maintenance of the disposal areas will include:
    a)
    periodic inspection of the disposal areas' surface includinq
    slopes;
    b)
    periodic inspection of the monitorinq well network and property
    fence;
    C)
    periodic mcwinq of the veqetation over the disposal areas'
    cover;
    d)
    the application of fertilizer at a specified frequency;
    e)
    re-establishment of veqetation over distressed areas;
    f)
    periodic repair of areas eroded by surtace water runoff,
    q)
    maintenance of the property fence and signs; and
    h)
    control of burrowinq animals.
    ~
    

    -------
    J
    9
    -; ;-
    G 0.j 3
    (I
    .-
    ..
    ~
    51 't IQ.IHO AA.
    ~1I.;'0IW:t....... ntOW "'tAT'WOIT 8I\..NI' 'tI
    ".aCTION ...c....s IitOT ~ ~ Q.MIn
    souacr' oj IOl'~6. [a,t )",.lO.".G..(
    .[''''.(U(I:. .,';s
    :! '[ "..wI ~1,o.O.""(j..(
    '(....usn JS.iS
    .
    (..~&CTlQfio C4
    .
    ;~ JH-SiTt/OJ"'-SlI't I1I(AT\IOIr~'
    ::3,-"RE : 9
    AL tERN A TIVt: '-REMEDIAL COMPONENTS I
    I
    FJ'I~U. "0 "(At\I("r ~t
    ..
    ,
    

    -------
    ,
    "
    EXTRACTION
    SYSTE"
    7~
    ~
    <:::=::: GROUNDWATER
    -.+.----.
    EQUALIZATION
    AND S£nuNG TANK
    ;t
    ~ ~ AIR INTAKE
    o~
    =>0
    uti!:
    ~
    SLUDGE HANDLING
    SYSTEM
    PUMP
    BLOWER
    0°0°0°
    0°r800
    o~ °
    °0°0°0
    °0°0°0
    °0°0°0
    °0°0°0
    ° ~o
    OO~oO
    OONdOO
    oONloO
    OO~~oO
    o 0
    00 000
    000
    --'
    2 STAGE VAPOUR PIIASE
    CARBOt4 ADSORPTION SYSTEM
    ,
    MIST
    EliMINA lOR
    1_--.__....
    ... -- --....
    ,
    9
    -~IOVlNI
    2 STAGE AQUEOUS
    PHASE CAlmON
    ADSORPTION
    SYSTEM
    DISCtfARGE
    --- .-. ~
    1'101](1-: ~o
    PROPOSED GROUNDWATER TREATMENT SYSTLM
    ~
    AIR STRIPPING
    COlUMN
    EfflUEN T
    S lORAGE TANK
    U1
    '-0
    C)
    c-'
    c,
    ~
    

    -------
    ~
    r
    )
    9
    . '-, '." \
    , I L ') :J
    ix)
    Identify and evaluate possible additional remedial actions requ~red
    for addressing the contam~natlon of the ent:re S~te ~nclud~ng the
    contaminant source (disposal areas) and possible environmental/
    ecological concerns and prepare a feasib~lity study to discuss the
    alternat~ves. possible treatao::ity stud:es and/or add:t:onal
    sampling may be requ~red.
    In additlon to the above activit:es, varlOUS support act:vities :ncluding the
    implementat~on of a worker health & safety program and env:ronmental mon:torlng
    for ind~cator chemlcal em~ss:ons will be conducted.
    The estimated costs of alternatives 2 and 6 are shown in Tables 15
    combined cost for this selected remedy, excluding the cost for the
    identified in paragraph ix above, is estimated to be approximately
    dollars.
    and 16. The
    work
    11,644,000
    Continqency Measures
    The goal of this remedial action is to restore the groundwater to its
    beneficial use, which is that of a drinking water source. Based on information
    obtained during the remedial investigation and the analysis of all remedial
    alternatives, EPA believes that the selected remedy may be able to ach:eve this
    goal.
    It may become apparent, during implementation or operation of the groundwater
    extraction system and its modifications, that contaminant levels have ceased to
    decline and are remaining constant at levels higher than the remediat~on goals
    in Table 12 over some portion of the contaminated plume. In such a case, the
    remediation goals and/or the remedy may be r~evaluated.
    If the selected remedy cannot meet the specified remediation goals, at any or
    all of the monitoring points during implen. tation, the contingency measures
    and goals described in this section may rep~ace the selected remedy and goals
    for these portions of the plume. such contingency measures will, at a minLmum,
    prevent further migration of the plume and include a combination of conta:nment
    technologies and institutional controls. These measures axe considered to be
    protective of human health and the environment, and axe technically pract~cable
    under the corresponding circumstances.
    The selected remedy will include groundwater extraction for an estimated per~od
    of 30 years, during wbicb time the system's performance will be carefully
    monitored on a regular basis and adjusted as warranted by the performance data
    collected during operation. MOdifications may include any or all of the
    followingl
    a)
    at individual wells where cleanup goals have been attained, pump:ng
    may be discontinued;
    b)
    alternating pumping at wells to eliminate stagnation points;
    C)
    pulse pumping to allow aquifer equilibration and encourage adsorbed
    contaminants to partition into groundwater; and
    d)
    installation of additional extraction wells to facilitate or
    accelerate cleanup of the contaminant plume.
    ,
    

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    5
    9
    Q 0 ,S G
    TABLE ~S
    REMEDIAL COST ESTThiA TE. At TER.'iA TIVE A2.
    HARDEMA.'l COlJ~ lA.'iDFILL SITE
         .4""1<411  Prts~t Worth  T.Jt4l1 Prutflt
    1 ttm Ducri p ti Oft  C4Ip"t4l1 Costs  O&M Costs  of O&M Costs  Worth Costs
    1. !I1stiN[ional Conrrols S 3.5,000 S 68 ,COO S 641.000 S 67"6.C(()
    ~ ~1aintain Existing Clay Cap    9 ,COO   as ,000  8= C(()
    3. On-Site Hydraulic Containment  550,000  25 ,000  US,.500  ;- 55 ,.5.)J
    4. Groundwater Treatment  1 ,J8S ,cro  325,000  3 ,064 ,cro   H49,ro::J
    5. Discharge  200,000  10,COO  94,000  294.ro::J
    6. !I1direct Capital Costs  976.300  °  °  9iL,,"'(J
     Subtotals S 3,146,500 5 ~37,COO 5 4,120,000  
     Total &timated Present Worth C08t . Altemative A2.     S 7,266,(0)
    ..
    

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    -59-
    5
    9
    ,0067
    TABLE 16
    R£',.~ro[AL COST ESTIMATE. ALTERNATIVE ("
    HARD£',.{A." COl::-.n L\:-.iDFILL SITE
         "'""11,,1  Pru"t Worth  Tot"l Prtsmt
    ftrm Drscr;pho"  CiJp"t,,[ Costs  O&M Costs  of O&.~ Costs  Worth Costs
    1. ::"cstit1Jtional Controls S 40 ,COO S l09,COO S 1.028,COO S 1.:60 ,COO
    , Off-Site Hydraulic Removal  970,COO  40 ,COO  377.COO  U47.XO
    3. Groundwater Tn!atment  2i5,COO  100 ,COO  94J,COO  1.2:8,COO
     (additiona! costs)        
    .{. Discharge  50,000  10,000  94 ,COO  144.COO
    5. lr1direct Capita! Costs  601 ,COO   0  0  60 1. COO 
     Subtotals S 1.9J6,COO S 259,COO S 2,-44:,COO  
     Totoll utimolt~d Pres~nt Worth Cost. Alt~matin"'"     S 40378,000
    ,
    

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    5
    9
    ,0068
    -60-
    To ensure that the remediation goals continue to be maintained, the aquifer
    will be monitored at those wells where pumping has ceased on an occurrence of
    every quarter for 5 years following di~continuation_of groundwater extraction.
    If it is 'determined, on the basis of the preceding criteria and the system
    performance data, 'that certain portions of the aquifer cannot be restored to
    their benet'icial use, any or all of the following measures invclving long-term
    management may occur, for an indefinite period of time, as a modification of
    the existing system:
    a)
    engineering controls such as physical barriers, or long-term
    gradient control provided by low level pumping, as containment
    measures;
    b)
    chemical-specific ARARs will be waived for the cleanup of those
    portions of the aquifer based on the technical impracticability of
    achieving further contaminant reduction;
    C)
    institutional controls will be provided/maintained to restrict
    access to those portions of the aquifer which remain above
    remediation goals;
    d),
    continued monitoring of specified wells; and
    e)
    periodic reevaluation of remedial technologies for groundwater
    restoration.
    The decision to invoke any or all of these measures may be made during
    periodic review of the remedial action, which will occur at leAst once
    five (5) years. If any or all of these measures are determined to be
    necessary, an Explaination of significant Differences ("ESD"), or a ROD
    Ammendment will be issued to inform the public of these actions.
    a
    every
    STATUTORY DETERMINATIONS
    Under its legal authorities, EPA's primary responsibility at superfund sites is
    to undertake remedial actions that achieve adequate protection of human health
    and the environment. In addition, section 121 of CERCLA establishes several
    other statutory requirements and preferences. These specify that when
    complete, the selected remedial action for this site must comply with
    applicable or relevant and appropriate environmental standards established
    under Federal and State environmental laws unless a statutory waiver is
    justified. The selected remedy also must be cost effective and utilize
    permanent solutions and alternative treatment technologies or resource recovery
    technologies to the maximum extent practicable. Finally, the statute
    includes a preference for remedies that employ treatment that permanently and
    significantly reduce the volume, toxicity, or mobility of hazardous wastes as
    their principal element. The following sections discuss how the selected
    reme~y meets these statutory requirements.
    protection of Human Health and the Environment
    Based on tbe site risk assessment, long term exposure to contaminants through
    the consumption and use of contaminated groundwater is the identified risk
    associated with the Site. Althougb no excessive risk was identified for
    exposure to the wastes contained in the disposal areas, th~s risk level was
    ~
    

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    5
    9
    0069
    -~~-
    based on present conditions which include a temporary cover over the disposal
    areas.
    The selected remedy protects human health and the environment through
    extract~on and treatment of the contaminated groundwater. The contaminants
    will be permanently removed from the groundwater by air str~pp~ng. The
    volatile d~ssolved gases w~ll be transferred to the air stream for treatment by
    carbon adsorpt~on and release to the atmosphere in compliance with Clean A~r
    Act regulations.
    Extraction of the contaminated groundwater also will eventually eliminate the
    threat of exposure to the most mobile contaminants from direct contact or from
    ingestion of contaminated groundwater. The future carcinogenic r~sks
    associated with these exposure pathways are as high as a one in one for
    consumption of the contaminated groundwater. By extracting the contam~nated
    groundwater and treating, the cancer risk in the consumption of off-site
    groundwater will be reduced to about 8.2 X 10-5 and an Hazard Indices (HI)
    ratio of less than 1. These levels are within the range of acceptable exposure
    levels of between 10-4 and 10-6 and an HI ratio of less than 1. There are
    no short-term threats associated with the selected remedy that cannot be
    readily controlled. In addition, no adverse cros.-media impacts are expected
    from the remedy.
    The contingency r~medy, if required, will provide overall protection of
    health and the environment through a combination of ma.. reduction and
    institutional and/or engineering control..
    human
    Compliance with ARARs
    The selected remedy of hydraulic containment and treatment
    groundwater at the PCC and extraction and treatment of the
    beyond the PCC will comply with all Applicable or Relevant
    Requirements (ARAR8) or the contingency remedy will attain
    waiver of any ARARs. The ARARs are pre.ented below:
    of the on-site
    off-site groundwater
    and Appropriate
    or justify the
    Action specific ARARs:
    *
    clean Water Act (40 CFR Part 122)
    *
    Tenne..ee water Quality Control Act, TN code 69-3-104
    *
    clean Air Act (40 CFR Parts 50-62)
    Chemical Specific ARARs:
    *
    Safe Drinking Water Act (40 CFR Part. 141, and 143)
    *
    Tenne..ee Water Quality criteria (1200-4)
    Location specific ARARs
    *
    Response in a Floodplan or wetlands (40 CFR Part 6, Append~x A)
    *
    RCRA (40 CFR Section 264.95)
    *
    clean Water Act (section 404) (40 CFR Part 230) (33 CFR Parts
    320-330)
    ,
    

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    -62-
    5
    9
    0070
    RCRA LDRs are not generally applicable to the groundwater extraction and
    treatment process; however, should levels in the waste residuals in the sludge
    from the treatment process exceed allowable standards, the sludge will be
    disposed of in accordance with LDRs.
    Cost Effectiveness
    The selected remedies are cost-effective because they have been determined to
    provide overall effectiveness proportional to their costs. Alternatives 2 and
    6 have an estimated net present worth value of $11,644,000. Alternative 6 is
    the least costly and the mostly easily implemented of Alternatives 4,5 and 6
    which meet all off-site ARARs.
    Utilization of Permanent solutions and Alternative Treatment Technoloqies (or
    Resource Recoverv Technoloqies) to the Maximum Extent practicable
    The State of Tennessee and EPA have determined that the selected remedy
    represents the maximum extent to which permanent solutions and treatment
    technologies can be utilized in a cost-effective manner for op Unit i1. of
    those alternatives that are protective of human health and the environment and
    comply with ARARs, the state of Tennessee and EPA have determined that this
    selected remedy provides the best balance of tradeoffs in terms of long-term .
    effectiveness and permanence, reduction in toxicity, mobility, or volume
    achieved through treatment, short-term effectiveness, implementability, cost,
    also considering the statutory preference for treatment as a principal element
    and considering state and community input.
    The selected remedy reduces the toxicity, mobility, and volume of the
    contaminants in the groundwater: complies with ARARs; provides short-term
    effectiveness; and protects human health and the environment. The selected
    remedy will be easier to implement technically because it requires less
    construction and is less likely to destroy the wetlands around clover creek.
    Finally, the off-site portion of the remedy costs the least of the equally
    protective off-site alternatives. The major tradeoffs that provide the basis
    for this selection decision are long-term effectiveness, implementability, and
    cost. .
    The selected remedy is more reliable and can be implemented more quickly, with
    less difficulty and at less cost that the other treatment alternatives and is
    therefore determined to be the most appropriate solution for the contaminated
    groundwater caused by the release of hazardous substances from or at the site.
    Preference for Treatment as a principal Element
    By treating the contaminated groundwater in an on-site treatment plant
    consisting of an air stripper and carbon adsorption then discharging the
    treated effluent to one of the nearby surface water bodies, the selected remedy
    addresses the principal threat of future direct contact/ingestion of
    contaminated groundwater posed by the site through the use of treatment
    technologies. Therefore, the statutory preference for remedies that employ
    treatment as a principal element is satisfied.
    ~
    

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