April 1988                            EPA-330/2-88-036
Hazardous Waste Ground-Water
Task Force
Evaluation of
U.S. Pollution Control, Inc.
Grassy Mountain Facility
Utah
                          U.S. Environmental Protection Agency
                              Library (PL-12J)
       UNITED STATES ENVIRONMENTAL PROTECTION AGENCY


       UTAH DEPARTMENT OF HEALTH

       BUREAU OF SOLID AND HAZARDOUS WASTE

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    UPDATE OF THE HAZARDOUS WASTE GROUND-WATER TASK FORCE
             EVALUATION OF U.S. POLLUTION CONTROL, INC.
                      GRASSY MOUNTAIN FACILITY

                             May 12, 1988
,       The Hazardous Waste Ground-Water Task Force (Task Force) of the
 United States Environmental Protection Agency (EPA), in conjunction with the
 Utah Department  of Health Bureau of  Solid and Hazardous Waste (UDH),
 conducted an evaluation of the ground-water monitoring program at the U.S.
 Pollution Control  Incorporated (USPCI) Grassy Mountain hazardous waste
 treatment, storage  and disposal facility. The Grassy Mountain facility is located
 approximately 80  miles  west of Salt  Lake City, Utah in the Great Salt Lake
 Desert.  The onsite field inspection was conducted during the period June 23
 through  1 7, 1 986 and July 9 through 11,1 986.

       USPCI is one of 58 facilities evaluated by the Task Force for compliance
 with applicable State and Federal ground-water monitoring requirements. The
 Task Force effort  originated in light of concerns as to whether operations of
 hazardous waste treatment, storage and disposal facilities are complying with
 State and Federal  ground-water monitoring requirements.

       The objectives of the Task Force evaluation were to:

       •     Determine compliance with  interim status ground-water monitoring
            requirements of Title 40 of the Code of Federal  Regulations,
            Part 265, Subpart F (40 CFR 265), as promulgated under RCRA
            and the equivalent State  requirements

            Evaluate the ground-water monitoring program described in the
            RCRA Part B permit  application submitted  by the Company for
            compliance with 40  CFR  270.14(c) and  the equivalent  State
            requirements

            Determine  if the ground  water beneath the  facility  contains
            hazardous waste or hazardous waste constituents

       •     Provide information  to assist the Agency in determining  if the
            TSDF meets EPA ground-water monitoring requirements  for waste
            management facilities receiving waste from response actions
            conducted  under the Comprehensive Environmental Response,
            Compensation and Liability Act, as amended (CERCLA)

       The Task Force prepared the  accompanying report on its evaluation,
 which  revealed  a number of deficiencies  in the ground-water monitoring
 program at the Grassy Mountain facility.  EPA Region VIII and UDH personnel
 had previously identified  many of the deficiencies that are discussed in the Task
 Force  report.  In the process of writing a RCRA permit for the  facility, the

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 regulatory agencies have tried to address those deficiencies and develop an
 appropriate ground-water monitoring program at Grassy Mountain.

      The  major  deficiencies  have  been  addressed  through requiring
 modification of operations through the permitting  process.  The RCRA draft
 permit for  the  USPCI Grassy  Mountain facility has  been written  and is
 undergoing modification prior to final permit issuance in 1988.

 Determine Compliance with the Ground-Water Monitoring Requirements of 40
 CFR. Part 265 and the Equivalent State Requirements

      The  Task Force evaluation  revealed  that  USPCI was not  in full
 compliance with  the ground-water monitoring  requirements of  40 CFR, Part
 265 and the equivalent State requirements in the Utah Hazardous Waste Rules
 7.13.  Deficiencies were found  in the sampling and analysis  plan and the
 implementation of that plan, sample analyses, the assessment monitoring plan
 and the monitoring system.

      The Task  Force found that several monitoring wells included in the
 sampling plan for Grassy  Mountain may have settled, causing changes in the
 elevations of the surveyed measuring points on the wells. Since the Task Force
 inspection, USPCI has extended most of the wells an additional 2.5 feet above
 ground.  The extensions  were accomplished  in  March  1987 and were
 resurveyed  at that time.  The final RCRA facility permit will require an  annual
 survey of all well elevation measuring points.

      The highly saline (greater than 70,000 ppm) ground water beneath the
 Grassy Mountain facility has created problems  with standard analyses  for the
 indicator parameters required by 40 CFR 265.92 and for metals and inorganics.
 The  Task Force recommendations for  changes  to  sampling  and analytical
 protocols will be incorporated into the final USPCI RCRA permit and will  require
 USPCI to monitor for specific volatile and semivolatile organics parameters in
 lieu of TOX as an indicator parameter.

      USPCI completed over a year of quarterly assessment  monitoring in
 1986 and 1987, using GC/MS analysis for volatile and semivolatile Appendix IX
 constituents as well as analyses for metals and other inorganics.  In addition to
the two sampling periods prior to the Task Force inspection, USPCI completed
four subsequent quarterly  samplings and associated analyses. EPA, the State
 and  USPCI agreed  that after assessment,  USPCI would continue to do
quarterly interim status monitoring until issuance of the RCRA permit, using the
same parameters  and analytical  methods as those  used for assessment
 monitoring.                     -  ™

      Following a meeting between EPA, the State and USPCI on March 30
and 31,1987, USPCI was instructed by EPA Region VIII to complete a report on
the results of the ground-water assessment monitoring program, as required by
40 CFR 265.93(d)(5).  USPCI submitted the assessment monitoring results to
UDH in May 1987.  A decision on how to proceed with ground-water monitoring

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will be made by UDH, pending the final results from an April 1988 Compliance
Monitoring Evaluation (CME).

      With respect to sample  analysis, the NAL laboratory has been instructed
by EPA Region VIII to identify specifically which  compounds it is capable of
analyzing.  In addition, the USPCI RCRA permit specifies which Appendix IX
and other GC/MS parameters will be monitored during the term of the permit.

      The Task Force report identifies critical deficiencies in the documentation
of the initial well monitoring system MW-1 through  MW-8.  Following the State-
USPCI Consent Agreement of October 1985, monitoring wells MW-9 through
MW-25 were installed. These  wells met regulatory objectives.  Additional wells
have  been installed since 1986  which  also meet the  regulatory  objectives.
MW-1  and MW-2 will continue as upgradient wells (new wells  MW-9 and
MW-20 are  used also).  MW-5  will  continue as one  of four downgradient
monitoring wells  at  the land treatment area; MW-6 may  be used  for a
nonregulated unit or may be  replaced.   Without any of the initial monitoring
wells, the remaining wells are  considered  adequate for monitoring needs.  This
monitoring system will remain  in effect for the duration of interim status and for
the term of the permit; wells may be added as disposal operations expand.

Evaluation of the Ground-Water Monitoring Program  Described in the RCRA
Part B for Compliance  with  40  CFR 27Q.14(c)  and  the  Equivalent  State
Requirements

      The RCRA permit will require detection  monitoring  under 40 CFR 264,
modified to include the GC/MS methods for volatile and  semivolatile organic
parameters (108 constituents)  as detection monitoring  parameters.  Metals and
inorganic  parameters will also be simultaneously collected semiannually,
although the regulatory agencies recognize that the  reliability of these
measurements is limited as a  result of the naturally high salinity of the ground
water.

      The permit contains  a specific statistical evaluation  protocol for the
monitored chemical constituents.   USPCI  has not  submitted  statistical
comparisons during interim status, however, based on the April 1988 CME,
USPCI was requested to submit a statistical comparison on all future monitoring
events.

Petermine if  the Ground Water Beneath the Facility Contains Hazardous Waste
or Hazardous Waste Constituents

      Analyses of ground-water samples have not shown that hazardous waste
or hazardous waste constituents  have entered the ground water beneath the
facility.

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Provide Information to Assist the Agency in Determining if the TSDF is Suitable
for Receipt of CERCLA Waste

      EPA Region VIII has determined that the USPCI Grassy Mountain Facility
may receive CERCLA waste.

      This update completes the Task Force evaluation of the USPCI Grassy
Mountain facility.

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UNITED STATES ENVIRONMENTAL PROTECTION AGENCY
HAZARDOUS WASTE GROUND-WATER TASK FORCE
EPA-330/2-88-036

GROUND-WATER  MONITORING  EVALUATION
U.S. POLLUTION CONTROL, INC.
Grassy Mountain Facility
Clive, Utah
April 1988
Sally C. Arnold
Project Coordinator
National Enforcement Investigations Center

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                          CONTENTS


EXECUTIVE SUMMARY


INTRODUCTION	1

SUMMARY OF FINDINGS AND CONCLUSIONS	6

     GROUND-WATER MONITORING PROGRAM DURING INTERIM
       STATUS	6

          Ground-Water Sampling and Analysis Plan	7
          Monitoring Wells	8
          USPCI Sample Collection and Handling Procedures	10
          Samples Analysis and Data Quality Evaluation	12
          Ground-Water Quality Assessment Program	15

     GROUND-WATER MONITORING PROGRAM PROPOSED FOR
       FINAL PERMIT	15
     TASK FORCE SAMPLING AND MONITORING DATA EVALUATION	18
     SUITABILITY FOR RECEIVING WASTES FROM CERCLA ACTIONS.... 18

TECHNICAL REPORT


INVESTIGATION METHODS	19

     RECORDS/DOCUMENT REVIEW	19
     FACILITY INSPECTION	20
     LABORATORY EVALUATION	20
     GROUND-WATER AND LEACHATE SAMPLING AND ANALYSIS	20

WASTE MANAGEMENT UNITS AND FACILITY OPERATIONS	26

     WASTE MANAGEMENT UNITS	26

          Surface Impoundment	29
          Landfills	31
          Tanks	37
          Drum Storage Area	39
          Land Treatment Areas	39

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                        CONTENTS (Cont.)
     FACILITY OPERATIONS	39

          Surface Impoundment	39
          Landfills	:40
          Tanks	40
          Drum Storage Area	41
          Land Treatment Areas	42

SITE HYDROGEOLOGY	43

     HYDROGEOLOGIC UNITS	44
     GROUND-WATER FLOW DIRECTION AND RATES	45

GROUND-WATER MONITORING PROGRAM DURING INTERIM STATUS	50

     REGULATORY REQUIREMENTS	53
     GROUND-WATER SAMPLING AND ANALYSIS PLAN	54

          Elements of the USPCI Sampling and Analysis Plan	54
          Sampling Records During Interim Status	56

     MONITORING WELLS	58

          Well Construction	59
          Well Locations	66

     USPCI SAMPLE COLLECTION AND HANDLING PROCEDURES	67

          Water Level Measurements	68
          Purging	70
          Field Data and Sample Collection	71
          Shipping and  Chain-of-Custody	74
          Sampling  and Analysis Plan	74

     SAMPLE ANALYSIS AND DATA QUALITY EVALUATION	75
     GROUND-WATER QUALITY ASSESSMENT PROGRAM	75

GROUND-WATER MONITORING PROPOSED FOR FINAL PERMIT	78

     PROPOSED MONITORING WELL NETWORK	78
     PROPOSED SAMPLING AND ANALYSIS PROGRAM	80

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                         CONTENTS (Cont.)
EVALUATION OF MONITORING DATA FOR INDICATIONS OF WASTE
   RELEASE	82
REFERENCES
APPENDICES

A    USPCI SAMPLE ANALYSIS AND DATA QUALITY EVALUATION
B    ANALYSIS AND DATA EVALUATION FOR TASK FORCE SAMPLES
FIGURES

 1.  USPCI Grassy Mountain Location Facility Map	2
 2.  Monitoring Well Locations, June 1986	9
 3.  Disposal Units at USPCI	27
 4.  Surface Impoundment Leachate Detection System Details	30
 5.  Landfill Cell 2 Leachate Sump Details	35
 6.  Landfill Cell 2 Leachate Withdrawal System Details	36
 7.  Water Level Elevations June 1986	49
 8.  Monitoring Well and Lysimeter Locations	61
 9.  General Monitoring Well Construction (MW-9 through MW-25)	64
10.  Well Cap Assembly	69
                              in

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                           CONTENTS (Cont.)
TABLES
 1.   Sample Collection and Location Description Monitoring Well Data	21
 2.   Leachate Sample Description and Collection Location	22
 3.   Preferred Order of Sample Collection, Bottle Type and Presevative
         List	:	24
 4.   Hazardous Waste Disposed at USPCI, Grassy Mountain 1985	28
 5.   Existing RCRA Tanks, Capacity and Types of Waste Stored	38
 6.   Range of Values of Porosity in Unconsolidated Sediments	46
 7.   Ground-Water Flow Velocity Computed by USPCI Consultants	47
 8.   Regulatory Authority,  Requirements and Events During USPCI
         Interim Status	51
 9.   State and Federal Counterpart Interim Status Regulations	53
10.   Water Level Measurements Omitted, December 1985 - June 1986	57
11.   USPCI Interim Status Monitoring Wells - June 1986	60
12.   Construction Specifications for Monitoring Wells	62
13.   USPCI Quarterly Sampling Parameters	73
14.   Monitoring Wells Sampled by Task Force	83
15.   Leachate Sample Location Descriptions	.-.83
16.   Selected Compounds Found in Leachate Samples from the
         Leachate Detection System of Cell 2	84
                                 IV

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EXECUTIVE SUMMARY

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                            INTRODUCTION

      Concerns have been raised about whether commercial hazardous waste
treatment, storage and  disposal facilities  (TSDFs) are complying  with the
ground-water  monitoring requirements promulgated  under the Resource
Conservation and Recovery Act (RCRA).* In question is the ability of existing or
proposed ground-water monitoring systems to detect contaminant releases from
waste management units.  To evaluate these systems and determine the current
compliance status, the Administrator of the Environmental  Protection Agency
(EPA) established a Hazardous Waste Ground-Water Task Force (Task Force).
The Task Force comprises personnel  from EPA Office of Solid Waste  and
Emergency Response, Office  of Enforcement  and Compliance Monitoring,
National Enforcement Investigations Center (NEIC), Regional Offices and State
regulatory agencies.

      The first TSD facility the Task Force inspected in EPA Region VIII was the
U.S. Pollution  Control, Inc. (USPCI), Grassy Mountain Facility, Clive, Utah
located in the  Great Salt  Lake  Desert about 80 miles west of Salt Lake City,
Utah [Figure 1].   The onsite inspection was coordinated by personnel from
NEIC, a field component  of the EPA Office of Enforcement and Compliance
Monitoring, during the  period  June 23 through June  27, 1986 and July 9
through July 11, 1986. Personnel from the State of Utah Department of Health,
Bureau of Solid and Hazardous Waste,  and  EPA Region VIII also participated.
The objectives of this investigation were similar to those of other Task Force
investigations,  namely:

            Determine compliance with interim status ground-water monitoring
            requirements of Title 40 of the  Code of Federal Regulations  Part
           265 Subpart  F  (40 CFR Part 265),  as promulgated  under RCRA
           and the equivalent Utah Hazardous Waste Rules (UHWR 7.13)
    Regulations promulgated under RCRA address hazardous waste management facility
    operations, including ground-water monitoring, to ensure that hazardous waste
    constituents are not released to the environment.

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  NORTHERN

   GREAT

  SALT LAKE


   DESERT
                           APPROXIMATE DEBCrtT BOUNDARY
                            (•ป doflncd by Otophปnป, 1074)
 TERRACE x
UOUNTAIHS\
                         NEWFOUNDLAND
                           MOUNTAINS
        SILVER ISLAND
         MOUNTAINS
              USPCI
             GRASSY
            MOUNTAIN
            FACILITY
            Knolls Exit
  610     20

DISTANCE IN MILES
                          NORTH
     Figure 1.
           USPCI GRASSY MOUNTAIN
            FACILITY LOCATION MAP

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            Evaluate the ground-water monitoring program described in the
            RCRA Part B permit application, submitted by  the facility,  for
            compliance with 40 CFR Part 270.14(c) and UHWR 3.3.2(c)

            Determine if the  ground water beneath the facility  contains
            hazardous waste or hazardous waste constituents

            Provide information to assist the Agency in determining if the
            TSDF meets EPA ground-water monitoring requirements for waste
            management facilities receiving waste from response actions
            conducted under the  Comprehensive Environmental Response,
            Compensation and Liability Act (CERCLA), as amended*

To address these objectives, this Task Force evaluation determined if:

            The facility has developed and is following an adequate ground-
            water sampling and analysis plan.

            Designated RCRA- and/or State-required monitoring wells are
            properly located and constructed.

            Required analyses have been done properly on samples from the
            designated RCRA monitoring wells.

            The ground-water quality assessment program outline (or plan, as
            appropriate) is adequate.

      The land surrounding the Grassy Mountain facility is undeveloped desert
belonging to the U.S. Bureau of Land Management.  A Hill Air Force Base
bombing range is located just  north of the  site.  This area has no residential
population.
     EPA policy, stated in May 6, 1985 memorandum from Jack McGraw on "Procedures for
     Planning and Implementing Off site Response" requires that TSDFs receiving CERCLA
     waste be in compliance with applicable RCRA ground-water monitoring requirements.

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      In 1981, USPCI leased the approximately 1-square-mile tract (643 acres)
from   Khosrow  Semnani,   who   attempted   to  develop  a   metals
reclamation/recovery  operation.  Semnani had acquired, but not set up, some
processing equipment. Some test drilling had been completed in the area and
two gondolas (roll-off boxes) of "waste"  had been brought to the site.  These
activities occurred in what became  a  206-acre  land treatment area.  For
purposes of RCRA interim status ground-water monitoring, eight wells were
installed at the site in 1981.

      USPCI submitted  a RCRA Part A application in December 1981  and
began hazardous waste management activities at the Grassy Mountain facility
in  March 1982.  Initial  operations were limited to storage and landfilling of
waste.  Land treatment began in April 1982.  Liquid waste neutralization and
sulfide treatment  began  in 1985.   Landfilling  of polychlorinated biphenyls
(PCBs) began in April 1986.  PPM, Inc., a subsidiary of USPCI, began operating
a liquid PCB treatment system at the Grassy Mountain site  in 1986.  All of the
above activities were ongoing during the Task Force inspection.

      The Grassy Mountain facility has been regulated by State waste disposal
 requirements since operations began. Currently, the site is operated  pursuant
 to interim status  regulations promulgated under the Utah Code Annotated
 Title 26 - Health  Chapter 14  rules (UC 26-14).*  The  Utah Department of
 Health (UDH) received RCRA interim authorization in December 1980 and final
 authorization in September 1984.   EPA  administers regulatory programs
-pursuant to the Hazardous and Solid Waste Amendments of 1984 and the
 Toxic Substances Control Act (TSCA).

      USPCI currently operates as an interim  status facility  under EPA
 Identification Number UTD991301748.   The Company  initially submitted a
 RCRA Part B permit application to EPA Region VIII and UDH in August 1983; a
 revised Part B was submitted in July 1984.
    The State equivalent of RCRA is the Utah Code Annotated Title 26 - Health Chapter 14
    rules (UC 26-14).  The State equivalents of Title 40 Code of Federal Regulations, Parts 260-
    265 are the Utah Hazardous Waste Rules (UHWR).

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     Upon receipt and review of the revised Part B, UDH and EPA Region VIII
determined that, among other things, the ground-water monitoring system was
deficient. In August 1985, the UDH sent a stipulation and consent order to the
Company  requiring them to  upgrade the existing ground-water monitoring
system.  A complaint paralleling the  State  action was filed by EPA in
September 1985.  On October 2, 1985, the Company signed a stipulation and
consent order to install a new ground-water monitoring system by November 8,
1985.

     Ground-water monitoring data from October 1984 samples showed  a
statistically  significant increase of total organic carbon (TOC) in  ground-water
monitoring well 3 (MW-3). On October 31, 1985, USPCI was ordered to initiate
an assessment monitoring program by the  Utah Department  of Health.
Therefore, the facility was in ground-water assessment monitoring under Utah
Hazardous Waste Rules 7.13.4 (UHWR 7.13.4) and 40 CFR 265.93 during the
Task Force inspection. The assessment monitoring consisted of  sampling and
analyzing for an increased number of parameters for  all the ground-water
monitoring wells as well as increased sampling for MW-3.

     Waste management operations for the nonhazardous USPCI industrial
landfill  are  regulated by Utah Solid Waste Management Regulations.  There
were no State or Federal permits for air emissions or water discharges, but the
State will issue an air permit in  1988.  A TSCA permit for treatment and
disposal of  PCB waste was issued to the Company by EPA on November 26,
1985.  Additional  permits include a Tooele County Conditional Use Permit
(number 100-81)  issued on  February 11, 1981  and  amended August 12,
1981; and  a  right-of-way permit from  the  United States Bureau  of  Land
Management (number U-47260) issued October 23, 1986.

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             SUMMARY OF FINDINGS AND CONCLUSIONS

     The findings and conclusions presented in this report reflect conditions
existing at the facility in June 1986. Actions taken by the State, EPA Region VIM
and USPCI subsequent to June are summarized in the accompanying update.

     Task Force personnel inspected the Grassy  Mountain facility  from
June 23 through June 27, 1986.  From July 9 through  July 11, 1986,  Task
Force personnel observed quarterly ground-water sampling to verify that a new
sampling and analysis plan was being implemented.

     The interim status ground-water monitoring program was evaluated  for
compliance on the basis of the Utah Hazardous Waste  Rules (UHWR 7.13),
which are equivalent to the Federal Regulations (40 CFR  Part 265, Subpart F).
The UHWR have governed the development of the ground-water monitoring
program since the beginning of hazardous disposal operations at the facility in
March  1982.  No hazardous waste disposal permit had been issued by the
State by the end of the onsite inspection.

     The inspection revealed that the  USPCI interim  status ground-water
monitoring program was  inadequate from the beginning  of waste disposal
operations in 1982.  The  Task Force found that as of July 1986, the interim
status  ground-water monitoring program components, including  the ground-
water sampling and analysis plan, the ground-water assessment program and
assessment program outline, did not comply  with State of Utah and RCRA
requirements. Most ground-water quality data obtained prior to the Task Force
inspection were not reliable.  These findings  are summarized here and are
detailed further in the technical  report.

GROUND-WATER MONITORING PROGRAM DURING INTERIM STATUS
     Major ground-water problems facing USPCI during interim status include
characterizing the ground-water quality at Grassy Mountain and implementing
a monitoring program that ensures adequate coverage of disposal units and
reliable analytical results. The reliability of water quality data from 1981 (when
USPCI leased the property) through 1985 is suspect because of both analytical

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deficiencies and interferences from the naturally high concentration of salts in
the ground water.  As a result, the true character of background ground-water
quality is not well understood.  Throughout this period,  USPCI continued
quarterly  monitoring with some analytical revisions in an effort to define
background water quality.

      In 1986, USPCI began a new effort to characterize the ground water
using more wells  and expanded analyses.   This  effort coincided with the
initiation of assessment monitoring triggered by elevated levels  of total organic
carbon (TOC) in MW-3.  At the request of EPA Region VIII  and the State, the
expanded analyses included additional organic parameters. The early  1986
water quality data,  although  showing  improvement over previous years,
continued to be deficient because  of analytical problems. The result is  a
shortage of reliable data characterizing  background ground-water quality at
Grassy Mountain as of mid-1986.

Ground-Water Sampling and Analysis Plan

      The ground-water sampling and analysis plan submitted in November
1985, in response to  an  October 1985 stipulation and consent order issued by
UDH, is inadequate.  The sampling and  analysis plan includes wells (MW-4,
MW-6, MW-7 and MW-8) that are no longer used. The sampling  and  analysis
plan also includes a four-page unreferenced list of Appendix VIII components;
the laboratory does not analyze for each of the listed parameters, neither does
the plan  indicate which of these parameters  are analyzed. Only the  list of
parameters  for which analyses actually are done should appear in the plan
and USPCI  should follow the plan by analyzing for  all the compounds listed.
More than one analytical method is listed for some parameters. The plan needs
to be revised to reflect which analytical methods are actually used.

     Methods in the plan for measuring static water levels, are acceptable
except for the provision that measurement accuracy  be obtained within 1/32 of
an inch (approximately 0.003 feet).  This accuracy is unrealistic  and cannot be
obtained with the electric water level indicator used by the facility.

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                                                                     8
     The plan provisions for field sampling are generally acceptable with the
exception of waiting until  all the  wells are  purged before sampling begins.
Some lag times may be necessary for slowly recharging wells; however, those
that recharge quickly should be sampled as soon as possible.

     The provisions for collecting field blanks need to state that field blanks be
preserved or not preserved, according to what is done for the corresponding
sample.  Otherwise the method  for field blanks is acceptable.

     The provisions for preservatives, chain-of-custody and shipping are also
acceptable.

Monitoring Wells

     Prior to 1986, the interim status ground-water monitoring system at
Grassy Mountain consisted of eight wells, MW-1 through MW-8. In early 1986,
12 new wells (MW-9 through MW-20) became part of the monitoring program at
Grassy  Mountain.   These new wells were constructed in  response to the
October 2, 1985 stipulation and consent order.  Wells MW-21 through MW-25
also were added in 1986.

     The monitoring well network  being  used during  the Task Force
inspection, included 23 (MW-1 through MW-23) of the  25 wells [Figure 2].  Two
additional wells (MW-24 and MW-25) were under construction at that time.
Exactly  which of these wells were being sampled for interim status ground-
water monitoring was unclear because Company personnel contradicted both
one another and their sampling  and analysis plan on this subject.

     In 1986, some of the older wells sampled prior to  1986 were dropped
from the  sampling program. Sampling records for 1986 were inconsistent and
did not show the same wells sampled each time. As a result, USPCI personnel
appeared not to know which of the earlier wells were still included for interim
status monitoring.

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                                           IMPOUNDMENT
f      LAB AND''/
           ACCESS ROAO
                                                          LANDFILL
                                                        MW-22
                                                           CELL X
                                                                      RUNOFF
                                                                     CONTROL
                                                                       PONO
                                              RUNOFF
                                              CONTROL!
                                               POND' I
                                                            ACCESS ROAO

                                                                   MW-9 •
                          LAND TREATMENT AREA II
                                                    LAND TREATMENT AREA I
                           LAND TREATMENT AREA III
                                                   LAND TREATMENT AREA IV
  Approximate Scale

600  300  0       600
    Monitoring Well
                  Figure 2.  Monitoring Well Locations

                                June  1986

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                                                                    10
      Information  available to the Task Force was insufficient to determine
whether monitoring wells MW-1  through MW-8 were properly constructed for
compliance with UHWR  7.13.2 (40 CFR 265.91).  If the information does not
exist, then  USPCI cannot  demonstrate that these wells were properly
constructed for ground-water  monitoring purposes  and  meet  regulatory
requirements.   The construction design and material for the new monitoring
wells (MW-9 through MW-23) are acceptable.

      The number and location of the wells in the network were determined to
be adequate to detect any statistically significant amounts of hazardous waste
constituents migrating to the uppermost aquifer from the waste management
units in place at the time of the Task Force inspection.  Additional wells will be
required as the facility expands the hazardous waste operations.

USPCI Sample Collection and Handling Procedures

      USPCI personnel did  not follow  their sampling and analysis plan with
respect to:   (1)pH  standardization,  (2) preservatives and (3) immediate
sample shipment.  By not following the plan, USPCI was out of compliance with
UHWR 7.13.3 (40 CFR 265.92).  Sampling procedures  in the  field were
careless  and  could potentially  compromise sample integrity.   Water level
measurements were inaccurate because of changing baseline  elevations
resulting from wells sinking and lack of precision in measuring water levels.

      The  pH of ground water beneath  the facility ranges from 7.1 to 7.5.  In
standardizing the pH meter, the standard at 7.4 and then the standard at 10.4
were  checked.  The meter should be  rechecked with the pH 7.4  standard to
ensure the instrument has not drifted in the 10.4 standard adjustments.  Also, in
order to follow the sampling and analysis plan, a standard in the pH range of
4.0 to 5.0 should be added to the calibration procedure. Measurements for pH
and  specific conductance are temperature-dependent.   Reported pH and
specific conductance results need  to  be corrected adequately  for  the
temperature of the sample at the time of measurement.

     The  shipping forms and labels on the sample bottles  for phenols from
National  Analytical  Laboratory  (NAL) list phosphoric  acid/cupric sulfate

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                                                                     11
 (HPO3/CUSO4) as  the  preservatives.*  The sampling and  analysis plan
 specifies H2SO4 as the preservative for phenols.   Better communication
 between the facility  and  the  laboratory  is needed to ensure that the plan
 matches the laboratory practices. Additionally, the plan needs to state that field
 blanks poured  for sample parameters  requiring preservatives  should  be
 preserved in a like manner to completely verify laboratory results.

      Sampling the monitoring wells requires  more than 1 day.  Samples are
 preserved and packed each day but are held for shipping up to 1 day and
 1  night  until sampling  is completed.  No samples  were held longer than
 prescribed in EPA guidelines (including shipping time); however, the sampling
 and analysis plan directs shipping immediately after collection and packing.

      USPCI personnel demonstrated their well purging techniques and water
 level measurement techniques during the June 1986 Task Force inspection.
 During the  July  1986 site visit  by the Task Force, USPCI personnel also
 demonstrated their sample collection techniques.  During  the July 1986 visit,
 new USPCI personnel were being trained  in the sampling  and handling
 procedures.

      At the time of the June and July 1986 site visits, USPCI personnel made
 water level measurements in the monitoring wells using an electric water level
 indicator.  The electric water  level indicator (ACTAT Olympic  Well Probe,ฎ
 Model 150) did not measure water levels with consistent accuracy. Task Force
 personnel repeatedly observed sequential  measurements in the same well that
 differed by as much as ฑ0.2 feet (measured with a tape measure). This margin
 of error is unacceptable for accurate water-level  analysis in conditions of a
 shallow hydraulic gradient such as the one at Grassy Mountain.

      Each well was equipped with a dedicated Well  Wizardฎ  bladder pump
 and wellhead assembly for purging and sampling.  For sampling required by
 UHWR 7.13.3 (40 CFR 265.92), USPCI personnel purged  all monitoring  wells
    NAL (Tulsa, Oklahoma) has done most of the ground-water analyses for the USPCI Grassy
    Mountain Facility.
ฎ   Olympic Well Probe and Well Wizard are registered trademarks and will appear hereafter
    without .

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                                                                     12
24  hours  or more before sampling began.  Sampling  should  be performed
immediately on any well that recharges rapidly in order to obtain fresh water
from the  aquifer.  Otherwise, chemical  reactions  may occur in water  that
stagnates in the well casing.  Wells that recharge slowly need to be sampled as
soon as a sufficient volume is available for sampling parameters.*  Although an
error in the sampling and analysis plan on procedures for computing the purge
volumes was noted by Task Force personnel, correct volumes were purged.
The USPCI sampling personnel wore latex surgical gloves that were discarded
upon contact with foreign substances and upon completing sampling of a well;
however, the inside of the sample containers and bottle caps were sometimes
touched by  the  samplers.  Anytime the inside of  a sampling container  is
possibly contaminated by contact  with a foreign  substance or a sampler's
finger, the container needs to be replaced by a clean one.

     Dedicated Teflonฎ sampling tubing was  stored inside most wellhead
assemblies.  At any well without dedicated tubing, the samplers utilized spare
tubing from their supplies.  In at least two cases, this tubing was reused without
rinsing between wells. The possibility of cross-well contamination is increased
greatly by  this practice and should be discontinued.

Samples Analysis anq1 Data Quality  Evaluation

     The  Task Force inspection revealed analytical inadequacies and found
that much of the ground-water monitoring between  1982 and June 1986 was
not performed  properly.  Most  of the  analytical  inadequacies  stem from
improper sample handling or calibration procedures, the lack of quality control
measures, and/or not accounting for the high dissolved solids content of the
sample. The high levels of dissolved solids can introduce variability to the data
and thereby have adversely affected the reliability of data in establishing
background levels or in detecting releases into ground water.
    RCRA Ground-Water Monitoring Technical Enforcement Guidance Document (TEGD),
    EPA, 1986, OSWER 9950.1
    Teflon is a registered trademark and will appear hereafter without ฎ.

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                                                                    13

      Ground-Water Analysis. 1982 through 1985

      Ground-water monitoring for  background water quality  in 1982 was
incomplete.  The quadruplicate measurements for the four indicator parameters
required by  UHWR 7.13.3 (40 CFR  265.92) were not reported.  Background
monitoring results  for the required pesticides, herbicides and radio-chemical
parameters  were  not reported (UHWR 7.13.3, 40 CFR  265.92).   Several
constituents were not  reported in one or more quarters [e.g., fluoride, nitrate,
pH, total organic carbon (TOC), total organic halogens (TOX), coliform, silver
and chromium].

      Long holding times for pH resulted because  USPCI shipped samples
from Utah to a laboratory in Oklahoma before measuring  pH (prior to  1984,
EPA recommended holding times of not more than 2 hours for wastewater and,
since that time, recommended measuring pH immediately).*  Measurement of
pH should be done in the field at the time of sampling.

      Specific conductance results  for 1982 through 1985 are suspect because
cell constant corrections were not  made for the measurements.  Standards to
establish the cell constant were not within the same range as the samples.

      Total organic halogens results for this  period are unreliable.  TOX
measurements using  the standard  method and instrumentation  for ground
water containing such high  levels of dissolved salts  and suspended solids
cannot  serve as an  indicator of low  level  contamination  of halogenated
organics.  Purgeable organic halogens  (POX) could serve as an indicator of
low level contamination of volatile halogenated organics (see Appendix A).

     Total organic carbon results for this period were  actually measurements
of nonpurgeable organic carbon.   The method of acidifying and  purging
samples prior to analysis eliminates purgeable organic carbon.
    (1)     40 CFR 136, Table II
    (2)     TEGD
    (3)     Procedures Manual for Groundwater Monitoring at Solid Waste Disposal Facilities.
    PB 84-17480
    (4)     Methods for Chemical Analysis of Water and Wastes. EPA 600/4-79-020

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                                                                    14
      Many  of the determinations for  metals prior to 1985 are  unreliable
because the high dissolved solids content of  the ground-water samples has
caused serious interferences  with the analytical methods (atomic absorption
spectroscopy techniques).  In 1985, the  laboratory began using Inductively
Coupled Argon Plasma Optical Emission Spectroscopy (ICP) which is also
subject to interferences from  high dissolved solids.  Neither method attained
detection limits low enough to establish background levels reliable for ground
water.

      A number of records for metals and pesticides determinations that were
performed on  ground-water  samples could not be found by the  laboratory
personnel.   The absence of  these  records prevented the Task Force from
evaluating the data quality for these parameters.

      Data reported  for the phenoxy acid herbicides 2,4-D and Silvex are not
reliable, as the method used  would not detect the herbicides present in-the
ester form.   In addition,  gross  alpha  and gross beta data are  unreliable
because levels are reported below what can be measured reliably in samples
containing percent levels of dissolved solids.

      Ground-Water Analysis Commencing January 1986

      Certain ground-water monitoring data for the first two quarters of 1986
were  absent.  No results were available for  MW-5 during the first quarter.
According to the  Utah Department  of Health, only volatile and semivolatile
organic compounds were reported for the second quarter for all the wells.

      Most of the laboratory findings applicable to the period prior to 1986
(discussed above) are also applicable to 1986 data, as most of the methods
did not change. Determinations still lacked adequate quality control measures.

      Volatile and  semivolatile organic results for the first two quarters of 1986
are unreliable.  The methods used (EPA Methods 624 and 625) were  not
properly followed.  Accuracy  and precision control measures required  by  the
methods were not  properly implemented or evaluated.

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                                                                   15

Ground-Water Quality Assessment Program

     Statistically significant elevated levels of total organic carbon (TOC) were
measured in  MW-3 on November 13, 1985.  A letter sent on December 12,
1985 by UDH notified USPCI that their ground-water quality assessment plan
should have been submitted  15 days after the initial notification, as required by
UHWR 7.13.4 (40 CFR 265.93).  USPCI only resubmitted the sampling and
analysis plan, which had been submitted in November 1985.  The sampling
and  analysis  plan does not  meet the requirements of a ground-water quality
assessment plan or programs, as required by UHWR 7.13.4 (40 CFR 265.93).
The plan does not:

           Specify for which organic compounds samples will be analyzed

     •     Identify the specific methods of analysis for organic compounds

           List and identify detection limits that  NAL is able to achieve  for
           each parameter analyzed

           Include  any  evaluation procedures  for the ground-water
           monitoring data, including analytical and water level data

           Make provisions for determining the rate and extent of migrations
           of the hazardous waste or constituents in the ground water

           Include complete and legible well construction specifications

     The  Grassy Mountain facility began a year  of quarterly assessment
monitoring  in the first quarter of 1986 but was  not following  an  approved
assessment monitoring plan.

GROUND-WATER MONITORING PROGRAM PROPOSED FOR FINAL PERMIT

     In May  1986, USPCI submitted a hydrogeologic characterization  report
for the  Grassy Mountain facility to UDH and EPA.  The report was  written to
satisfy  the Part B  ground-water requirements detailed in UHWR Part III
(40 CFR 270.14).  Although the report addresses the requirements, it is

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                                                                    16
inadequate in detail and revisions to the proposed ground-water monitoring
program will be necessary for the final RCRA permit.

     The report outlines a detection monitoring program pursuant to UHWR
8.6.9 (40 CFR 264.98) for the uppermost aquifer and describes the proposed
monitoring well network,  monitoring parameters, sample analyses, sample
collection and data evaluation. The Task Force considers detection monitoring
to be appropriate at Grassy Mountain.

     As  USPCI expands operations, the number of wells in the detection
monitoring program probably will increase.  For the October 1985 Stipulation
and Consent  Order, UDH and EPA Region VIII proposed dedicating wells to
monitor each regulated unit rather than monitoring all the units as a group.  The
regulatory agencies also propose placement of monitoring wells so that they
circumscribe the landfill cells  (as opposed to downgradient only)  in order to
provide radial detection coverage of ground-water mounds induced by landfill
loading.   This approach optimizes the chances  of  detecting leakage from
individual  units.

     Wells MW-4, MW-6  and MW-7 are several hundred feet  from  waste
management units and cannot provide immediate detection of leakage. These
wells are  not suitable to be included in the  regular ground-water monitoring
program proposed for the permit, however they may provide useful water level
data and periodic ground-water quality data.  For reasons stated in the section
entitled "Well Construction," USPCI was unable to demonstrate that monitoring
wells MW-1 through MW-8 were in compliance with UHWR 7.13.2 (40 CFR
265.91).

     For the land treatment areas, the existing downgradient monitoring wells
in the saturated  zone combined with the  16 lysimeters in the unsaturated zone
should be adequate for compliance with 40 CFR  264.278  (UHWR 8.13.9,
when written, will be the State's corresponding regulation for unsaturated zone
monitoring beneath a  land  treatment  area), and UHWR 8.6.8  and 8.6.9
(40 CFR 264.97 and 264.98).

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                                                                    17
     The Task  Force agrees with  the  identification of the "shallow brine
aquifer"  as  the  uppermost aquifer, as  defined by UHWR  Part 1 (40 CFR
260.10).   The proposed design for future monitoring  well construction is
acceptable.

     Leakage of hazardous waste  or hazardous waste constituents to the
ground water has not been substantiated; however, analyses of leachate
samples  drawn from between two synthetic liners of cell 2 indicate the upper
liner has failed.   USPCI must be prepared  to implement a compliance
monitoring program under UHWR 8.6.10 (40 CFR 264.99) in case the second,
lower liner of cell 2 or liners of other units fail.

     The list of proposed analytical parameters is too comprehensive  and
includes  compounds that are not analyzable by GC/MS. USPCI needs to
develop a list of parameters they can analyze and provide attainable detection
limits with each parameter listed.

     The analytical procedures used to date by  NAL have been judged by the
Task Force to be incapable of accurately  measuring hazardous constituents in
ground-water samples or of providing a reliable indication  of ground-water
quality.  For the permit, personnel from the NAL laboratory should assess the
laboratory capabilities  and protocols and propose analytical methods they can
do properly.

     The inconsistent  sampling procedures that existed prior to the Task Force
inspection cannot ensure monitoring results that  provide a reliable indication of
ground-water quality.   USPCI  needs to ensure consistent sampling  and
analytical procedures to comply with  UHWR 8.6.8 (40 CFR 264.97).

     USPCI has  proposed to  evaluate  ground-water analytical data
statistically using the  Chemical Manufacturers1-Assocfation-4CMA) standard
t-test.  This  procedure is inappropriate for the Grassy Mountain facility as it
does not account for variables such  as the naturally high salts in the ground
water and the apparently natural  fluctuations in ground-water quality.

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                                                                   18

TASK FORCE SAMPLING AND MONITORING DATA EVALUATION

     During the June 1986 onsite inspection, samples were collected by Task
Force contractors from 10 monitoring wells and 6 leachate collection sumps to
determine if the ground water contained hazardous waste constituents or other
indicators of contamination.  Water levels were measured  and samples were
drawn  from the wells and sumps by USPCI personnel using their standard
procedures.

     Analytical data for the Task Force samples from the monitoring wells do
not indicate the  presence of hazardous constituents in  the ground water
beneath the site.  Previously, statistically elevated levels of total organic carbon
were found in  well MW-3 by NAL; however, these elevated levels were not
substantiated by the Task Force sampling nor by additional monitoring  by the
Company.

     Task Force data for the leachate detection sump samples from  landfill
cell 2 indicated a leak of the upper synthetic landfill liner.   Data collected by
USPCI confirm that in landfill cell 2, such  a leak has occurred.  Ground-water
data, however, show no indication that the  lower synthetic liner has leaked.

SUITABILITY FOR RECEIVING WASTES FROM CERCLA ACTIONS

     Under current EPA policy, if an offsite TSDF is used for land disposal of
waste from a CERCLA site, that site must be in compliance with the applicable
technical  requirements of  RCRA.   During  the  Task Force inspection, the
ground-water monitoring program at the Grassy Mountain facility was being
conducted pursuant to the October 1985 Stipulation and Consent Order prior to
issuance of the final RCRA permit by the State.

     At the time of the Task Force inspection, the facility did not meet  all the
technical requirements for a  RCRA  ground-water monitoring program.  USPCI
was acting under State and  EPA orders, however, to develop a monitoring
program that conforms  to State and  Federal permit requirements (Parts 8.6
and 264, respectively).

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TECHNICAL REPORT

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                                                                   19

                      INVESTIGATION METHODS

      The Task Force evaluation of USPCI consisted of:

            Review and  evaluation of records and documents from EPA
            Region VIII, UDH and USPCI
      •     Facility onsite  inspection  conducted June 23  through  27 and
            July 9 through 11,  1986

            Offsite analytical laboratory evaluation

            Sampling  and  subsequent analysis  and data evaluation  for
            selected ground-water and  leachate monitoring systems


RECORDS/DOCUMENT REVIEW

      Records and documents from the UDH and EPA Region VIII offices,
compiled by an EPA contractor, were reviewed prior to an onsite inspection.
Facility records  also  were reviewed to verify  information currently  in
Government files and supplement Government information where necessary.
Selected documents requiring in-depth  evaluation were copied by the Task
Force during the inspection.   Records were reviewed to obtain information on
facility operations, construction of waste management units and ground-water
monitoring activities.

      Specific documents and records  reviewed and evaluated included the
ground-water sampling and analysis  plan  (SAP), a ground-water quality
assessment  plan, analytical  results  from  past  ground-water sampling,
monitoring well construction data and logs, site geologic reports, site operations
plans, facility permits, unit design and operation reports, and operating records
showing the general types and quantities of wastes disposed of at the facility
and the disposal locations.

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                                                                   20
FACILITY INSPECTION

      The facility inspection included identifying waste  management units,
waste management operations and pollution control practices, and verifying the
location of ground-water monitoring wells and leachate collection sumps.

      Company  representatives  were interviewed to identify records and
documents of interest, answer questions  about the documents, and explain:
(1) facility operations (past  and present), (2) site  hydrogeology,  (3) the
ground-water monitoring system, (4) the ground-water sampling and analysis
plan, (5) company procedures for assessment, and (6)  laboratory procedures
for obtaining data on ground-water quality.  Laboratory personnel from an offsite
laboratory that analyzed ground-water samples for USPCI were interviewed
regarding sample handling, analysis and document control.

LABORATORY EVALUATION

      The  USPCI-owned  National Analytical Laboratory (NAL)  in Tulsa,
Oklahoma,  was  evaluated  regarding  responsibilities  for analysis  of
ground-water samples from the Grassy Mountain facility.  Analytical equipment
and  methods,  quality  assurance  procedures  and documentation  were
examined for adequacy.  Laboratory records were inspected for completeness,
accuracy and for compliance with State and Federal  requirements.  The ability
of NAL to produce quality data for the required analyses was evaluated.

GROUND-WATER AND LEACHATE SAMPLING AND ANALYSIS

      During the  inspection, Task  Force personnel  collected samples for
analysis from  10  ground-water  monitoring  wells and 6 leachate collection
sumps [Tables  1 and 2] to determine if the ground water contained hazardous
waste constituents or other indicators of contamination. The sampling results
were used  in evaluating previous Company data.  Wells were selected for
sampling either in  areas where records suggest that  ground-water quality may
be or may  have been affected by hazardous waste management  activities.
Other wells were selected to confirm background ground-water quality.

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                                                                                                 21
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                                                                  22
Leachate sumps were sampled to the extent that sufficient liquid was present for
the samples. Duplicate volatile organic samples and splits of all other samples
were provided to USPCI personnel.
                               Table 2
     LEACHATE SAMPLE DESCRIPTION AND COLLECTION LOCATION
Leachate
Sump
Cell 1


Cell 2
1B

2B


3B

4B

Surface
Impound-
ment
Location
Southern end
of cell 1


Northeast
corner
Southeast
corner

Southwest
corner
Northwest
corner
West end


Date Time Remarks
6/24 1 040 Sample dark straw/amber
color with black sediment;
oily sheen on surface

6/23 1501 Sample clear; NEIC split

6/24 0914 Containers omitted: phenols
su If ate/chloride, nitrate,
ammonia, sulfides
6/23 1348 Sample light straw color

6/23 1 138 Sample grey in color

6/24 1 223 Sample grey in color; sedi-
ment present; collected
only three TOC* containers
      Total Organic Carbon

      Each of the monitoring wells was equipped with a dedicated Well Wizard
sampling pump, which was operated by USPCI personnel.  Samples were
collected from these wells  by the following procedure.  Additional details of
USPCI sampling procedures are described in the section  on Ground-Water
Monitoring Program During Interim Status.

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                                                                   23
      1.     Company personnel determined depth to ground water using an
            ACTAT Olympic Well Probe, Model 150.

      2.     Company personnel calculated the height of the water column
            from depth  to  water  measurement  and well  depth (from
            construction records).

      3.     Company personnel determined the water column volume using
            the formula:
                        volume = n (radius)2 (height of water column)

      4.     Company personnel purged three water column volumes.

      5.     After recharge,  EPA contractor monitored open well head for
            chemical vapors  (HNU) and radiation.

      6.     EPA contractor  collected sample aliquot and measured water
            temperature and  pH.

      7.     EPA contractor  filled sample containers in the order shown in
            Table 3, alternating  between  filling a  sample  aliquot  for the
            Company and one for the EPA contract laboratory. When NEIC
            samples were collected, the above  protocol  was modified to
            include filling a sample aliquot for NEIC after  filling one for the
            EPA contractor.

      8.     Samples were placed on ice in an insulated container.

      All sample containers were filled directly from the discharge line.  After
sampling was completed at a well, EPA contractor personnel took their samples
to a staging area where a turbidity measurement was taken and one of two
sample aliquots for  metals analysis was  filtered.  In addition, metals, TOC,
phenols, cyanide, nitrate and ammonia samples were preserved [Table 3].

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                                                                   24
                               Table 3
    PREFERRED ORDER OF SAMPLE COLLECTION, BOTTLE TYPE AND
                         PRESERVATIVE LIST
         Parameter
                                Bottle
Preservative
1.   Volatile organic analysis (VOA)
      Purge and trap
      Direct inject
2.   Purgeable organic
    carbon (POC)
3.   Purgeable organic,
    halogens (POX)
4.   Extractable organics
5.   Total metals
6.   Total organic
    carbon (TOC)
7.   Total organic
    halogens (TOX)
8.   Phenols
9.   Cyanide
10. Nitrate/ammonia
11. Su If ate/chloride
12. Radionuclides
    (NEIC only)
13. Sulfides
                         Two 60-ml VOA vials
                         Two 60-ml VOA vials
                         One 60-ml VOA vial
                         One 60-ml VOA vial
                         Four 1 -qt. amber glass
                         1-qt plastic
                         4-oz. glass

                         1-qt. amber glass

                         1-qt. amber glass
                         1-qt. plastic
                         1-qt. plastic
                         1-qt. plastic
                         Four 1-qt. amber
                         glass
HNO3
H2S04
H2S04
NaOH
H2SO
                                                 0.2 ml of 2N
                                                 acetate* solution
                                                 and 0.2 ml
                                                 NaOH
2 Normal Acetate Solution:
                                           in 870 ml Hฃ0

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                                                                   25
      Leachate was collected at sumps below the operating landfills 1 and 2,
and below the surface impoundment.  All leachate samples were collected prior
to collecting ground-water samples to prevent possible cross-contamination
between the two.  The EPA contractor collected composite samples in gallon
glass jugs then transferred the leachate to sample containers provided by the
EPA contractor. Leachate samples were not preserved.

      At the end of each day, samples were packaged and shipped to the two
EPA contract laboratories according to applicable Department of Transportation
(DOT) regulations (40 CFR Parts 171 through  177).  Samples from monitoring
wells were considered "environmental" and those from  leachate sumps were
considered "hazardous" for shipping purposes.

      At two sampling locations (MW-14 and MW-15), the EPA contractor
prepared field blanks for  each  analytical parameter group (e.g., volatiles,
organics,  metals) by pouring high  pressure  liquid  chromatography (HPkC)
water of known quality into sample containers.  One set of trip blanks for each
parameter group was also prepared and submitted during the inspection.  The
blanks were submitted to the laboratories with  no distinguishing labeling or
markings.

      Samples were analyzed by the EPA  contractor laboratories for the
parameter groups shown on Table 3 minus the groups indicated on Tables 1
and  2.  NEIC received  and  analyzed split samples for one ground-water
monitoring well (MW-14) and one leachate sump (cell 2, sump 1B).

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                                                                    26

        WASTE MANAGEMENT UNITS AND FACILITY OPERATIONS

WASTE MANAGEMENT UNITS

      The Grassy Mountain facility handles both hazardous waste, as defined
by the Utah Hazardous Waste Rules pursuant to the Utah Code Annotated
Title 26 - Health Chapter 14 (UC 26-14) and regulated by the UDH and EPA,
and  PCS waste, as defined in 40 CFR 761  and regulated by EPA. The Task
Force identified waste handling units and operations to determine where waste
constituents handled at Grassy Mountain might enter the ground water.  This
section describes the waste management units at the Grassy Mountain facility.

      During the Task Force inspection,  USPCI was using  the following
management  units/areas  for the  treatment, storage and/or disposal of
hazardous waste:

            One surface impoundment - storage
            Four landfills*- disposal
            Nine tanks - storage and treatment
      •     One drum storage area - container storage
      •     Four land treatment areas - disposal

      No waste handling operations existed prior to the enactment of RCRA, as
the site has accepted hazardous wastes only since 1982.  At the time of the
Task Force inspection, all operations and units ever used by USPCI were still
active [Figure 3], although landfill cell  1 was nearly full and expected to close
soon.  Hazardous wastes accepted by USPCI  in 1985 are  presented in
Table 4.
    Only two landfills were used for hazardous waste disposal. The other two landfills were
    used for PCBs or nonhazardous industrial waste and were not evaluated for compliance
    with Subpart F.

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                                                                                               27
.
     INDUSTRIAL

     WASTE

     LANDFILL

     CELL
                  ACCESS  ROAD
r
u
                                                 LANDFILL

                                                  CELL 2
                                                         /
    SURFACE'lf]
IMPOUNDMENT

    ''.LAB AND'''
                                                               /f
                 'Q>
                                                                  OFFICE
                                             "|  j LANDFILL
                                                i  CELL 1
                   RUNOFF
                  CONTROL.
                   I POND  i
                                                                                   ACCESS ROAD
                                      LANO TREATMENT AREA II
                                        LANO TREATMENT AREA III
                                                                        LANO TREATMENT AREA I
                                                                       LANO TREATMENT  AREA IV
                                               Figure -3
                                       DISPOSAL UNITS  AT USPCI

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                                                                         28
                                   Table 4
         HAZARDOUS WASTE DISPOSED AT USPCI, GRASSY MOUNTAIN, 1985
EPA Hazardous
Waste Number
DOOO
D001
D002
D003
D003/K049/K051

D004
D005
D006
D007 EP Toxic
D008 Waste
D009
D012
D013
D016
F001/F002
F003/F004/F005
F006/F008
F009/F019
K001
K037
K048/K049/K050
K051/K052
K061/K062
K087
U007
U036
U044
U051
U092
U151
U188
U220
U223
U230
U239
U240
U242
P012
Description of Waste
Miscellaneous hazardous waste
Igni table waste
Corrosive waste
Reactive waste
Reactive plus petroleum refining
waste
Arsenic waste
Barium waste
Cadmium waste
Chromium waste
Lead waste
Mercury waste
Endrin waste
Lindane waste
2,4-D waste
Spent halogenated solvents
Spent nonhalogenated solvents
Treatment sludges/solutions

Wood preservation waste
Pesticide waste
Petroleum refining waste

Iron and steel waste
Coking waste
Acrylamide
Chlordane
Chloroform
Creosote
Dimethylamine
Mercury
Phenol
Toluene
Benzene
2,4,6-Trichlorophenol
Xylene
2,4-D
Pentachlorophenol
Arsenic trioxide

Landfilled
109,624
745,042
4,155,313
273,826


1 1 ,782,274
35,996
1,757,595
3,145,664
701,601
9,320
4,119,067
333
42,858
172,817
262,496
929,108

809,697
543,140
16,853,317

9,563,800
705,702
225
508
959
486,615
2,020
500
9,200
617
500
19
3,073
2,524

1,022
Amount (pounds^
Tank Treatment Land Application

399,835
1.448 2,033,998

9,806,450



54,330
13,195





187,317
822,264




20,086 9,470,441

338,760













500

Source: 1985 Annual Report

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                                                                    29
      PCB  waste processing  and disposal operations included storage,
treatment and disposal.  Any storage and treatment of liquid PCBs is operated
by PPM, Inc., a subsidiary of USPCI.  PCB liquids are detoxified and shipped
offsite as a  fuel  oil blend.  As a result of the detoxification process, a spent
caustic  solution is generated that is used by USPCI for waste neutralization.
PCB  solids  (transformer carcasses, contaminated debris, etc.) are landfilled
onsite.

Surface Impoundment

      USPCI uses the  surface impoundment  for  liquid hazardous waste
storage prior to land treatment.   USPCI stores waste  water from refinery
processes in the impoundment and removes oil from the top, as necessary. The
surface  impoundment storage capacity is about 6.2 acre-feet (about 2 million
gallons).* The surface impoundment is subject to the ground-water monitoring
requirements of the UHWR interim status regulations.

      The USPCI site is underlain  by  lakebed sediments (primarily silty clay).
The surface  impoundment is mostly above grade with the bottom about 2 feet
below grade. USPCI constructed the embankment in 1982 from soil obtained
from  a  nearby ridge  consisting of  a mixture of  sands, silts and clays.  The
Company added and tested a 3-foot clay liner, leachate detection system and
synthetic liner in 1984 and 1985.

      The clay liner was constructed with clay from borrow areas on the
northwest portion of the property.  The clay was compacted, but no permeability
tests were done.

      The leachate  detection system was  constructed by  placing 8-inch-
diameter pipe with 1/4-inch holes on 1-foot centers in a gravel sump [Figure 4].
This  system was originally designed as a gravel relief vent system and was
modified for use as a leachate detection system.
    ,4s  reported  in a  USPCI September 28,  1984 transmittal  regarding Surface
    Impoundment A, Exhibit C

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                                                                                      30
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    DETECTION SYSTEM DETAILS
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                                                    SECTION B - B*

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                                                                     31
      The synthetic  liner  is 100 mil  High Density Polyethylene  (HOPE).
Compatibility testing conducted by consultants indicated the  HOPE liner was
compatible with solutions  similar to refinery wastewater; USPCI  proposed
impounding  refinery wastewater (EPA hazardous waste numbers K048-K051)
in this impoundment.  The State approved of this impoundment for storage of
petroleum refinery wastes on April  2, 1985.

      The impoundment is square with a finished bottom width of 115 feet, 3:1
side slopes and a total depth of 14 feet  (2 feet of freeboard are required, thus,
useable depth is 12 feet). The dike crest is about 14 feet wide and the outer
embankment has a  2:1  slope.   The dike top and outer embankment were
covered with a minimum of 4 inches of gravel.  The  impoundment bottom is
sloped toward the leachate collection system.  Waste levels in the impoundment
are mostly above ground and always above the water table.

      The surface impoundment has been in service since mid-1985.  During
the Task Force inspection, more than  a 2-foot freeboard  was observed.
Freeboard measurements are referenced by marks on a pump track for raising
or lowering the pump used to remove liquid from the impoundment.

Landfills

      Although there were  four  landfills at  the USPCI site, only two were
hazardous waste landfills (landfill cells 1 and 2) and subject to the RCRA interim
status ground-water requirements.  One landfill (industrial waste landfill cell)
was used  for burial of non-RCRA industrial waste and one landfill (landfill cell X)
was used for burial of PCB  solid  waste.*  Total capacity for the four existing
landfills was approximately 275 acre-feet.

      USPCI operates the landfills using a progressive slope  or ramp method
of landfilling where each layer is completed and compacted and the landfill is
filled from the bottom up.  Each landfill cell will be closed and capped after the
cell is full. Landfill cell 1  was almost full at the time of the inspection.  The first
    A fifth landfill cell (landfill cell 3), for burial of hazardous waste, was under construction during
    the Task Force inspection.

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                                                                     32
waste was placed in landfill cell  1 in March 1982; all other landfills went into
service after that date.

      Landfill Cell 1

      Landfill cell 1 is located in the middle of the northern half of the USPCI
facility.  The landfill was completed and began accepting waste in March 1982.
The landfill was expanded in 1984 by adding 10 feet in height to the cell.  Total
capacity of the expanded cell is about 29 acre-feet.

      The landfill was constructed  so that all  waste is buried above grade.
Existing soil (5 feet) was excavated for later replacement with  compacted clay.
At the bottom  of the excavation, three gas relief trenches were dug. These
trenches transect  the landfill cell under the clay liner.  The trenches  consist of
gravel surrounded with geotextile fabric and vented by vertical riser pipe.  The
embankment was  constructed with material taken from the same ridge of sands,
silts and clays, as  for the surface impoundment.  A 5-foot clay liner and a gravel
layer for leachate  collection and removal were installed after the embankment
was constructed.

      The ground surface to receive embankment material was scarified to a
depth of about 8 inches and recompacted.  Embankment and backfill material
were monitored for moisture content before compaction.  Moisture content
varied  more than original  design  specifications, but desired  compaction
densities (95% Standard Proctor) were almost always achieved.

      The clay liner was constructed with clay from a nearby borrow area that
complied with the  Unified Soil Classification of CL materials with an  additional
requirement that at least  80% of the material pass through a No. 200 sieve.
Liner material  moisture content  also varied but desired compaction densities
were achieved except for one test  which indicated 94% instead of 95% of
Standard Proctor.  Clay used for the  cell 1 liner may not have  met  permeability
standards. Although permeability tests conducted on two laboratory samples
indicated the clay liner has  a permeability less than  1  x  10~7 cm/sec, more
comprehensive field and laboratory testing on clay from  the  same  area
indicated  permeability was  greater than 1  x  10"7 cm/sec and sodium

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                                                                     33
 hexametaphosphate  had to be added to the clay to meet permeability
 standards.

      The top of the clay liner (bottom of the landfill) was crowned 6 inches to
 provided drainage to the edges for removal of rainfall. A 6-inch-thick layer of
 uniform size gravel  was placed over the clay  liner to  serve  as a  leachate
 collection and removal system;  however, no sumps or risers were installed to
 facilitate leachate removal.

      Landfill cell 1 is rectangular with finished bottom dimensions of 100 feet
 by 300 feet, 3:1 side slopes and a total depth of 22 feet.  The dike top is about
 18 feet wide and the outer embankment has a 2:1 slope. The dike top and outer
 embankment are covered with gravel.

      Landfill cell  1  has received various  solid, semi-solid and sludge type
 waste. Table 4 presents waste placed in both landfill cells 1 and 2. During the
 Task Force inspection, landfill cell 1  was almost full.  USPCI officials indicated
 they were waiting for an appropriate  waste such  as contaminated  soil to
 completely fill landfill cell 1 and provide a suitable  base  for  the cap to be
 installed during closure of the unit.

      Landfill Cell 2

      Landfill cell  2 is  located  directly  north of landfill  cell 1  and shares a
 common side.  The landfill was completed in 1984  and 1985.  Waste was
 landfilled in cell 2 beginning in September 1985.  Total capacity of landfill cell 2
 is about 62 acre-feet.

      The landfill was constructed so that all waste is buried above grade.  The
 natural ground surface was scarified to a depth of 8 inches and recompacted.
The  new  embankment was benched into  the  existing  embankment  where
 landfill cell 2 abuts landfill cell 1.   The embankment was constructed similarly to
the landfill cell 1 embankment with material from a  nearby borrow area.  The
 liner, in ascending order, consists of a 2-foot compacted clay  liner,  a 60-mil
 HOPE  liner,  drainage  net, a 60-mil HOPE liner, drainage net, non-woven
geotextile fabric  and  a  2-foot protective  sand  layer.    The leachate

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                                                                     34
collection/detection system consists of pipes and four secondary or detection
sumps between the synthetic liners and pipes, and four primary or collection
sumps on top of the synthetic liners [Figures 5 and 6].

      The clay liner was constructed with clay from a nearby borrow area. To
meet permeability requirements of 1 x 10~7 cm/sec  or less, sodium hexameta-
phosphate was added to the clay.  Permeability tests in the field (7.6 x 10~9 to
7.6 x 10"8 cm/sec) and laboratory (2.1 x 10~8 to 4.5 x 10~8 cm/sec) indicated the
clay liner has permeability less than 1 x 10"7 cm/sec.

      The top of the clay liner is sloped  radially to the four leachate collection
sumps.  The primary leachate collection system  is designed to collect any
leachate reaching the bottom of the cell.  The secondary leachate detection
system  is designed to collect any leachate  that has breached the uppermost
synthetic liner.  Any leachate collected in the secondary/detection system would
indicate a failure of the uppermost  synthetic liner.

      Landfill cell 2 is rectangular with finished bottom dimensions of 340 feet
by 375 feet, 3:1 side slopes and a total depth of 16 feet. The dike top is about
12 feet wide and the outer embankment has a 2:1 slope.  The dike top and outer
embankment are covered with gravel.

      USPCI has placed various waste into landfill cell 2 [Table 4]. During the
Task Force inspection, landfill cell 2 was  in service and USPCI was concerned
that leachate had been collected from the secondary leachate detection system
indicating a failure of the upper  synthetic  liner.  The Task Force collected
samples from  the  secondary  leachate detection system  for  analysis  to
investigate this concern.

      PCB Landfill Cell X

      The  PCB landfill  cell X is  located east of the  office in the  northeast
quadrant of the USPCI facility.   The unit  was built in 1985-86 and began
accepting waste  in April  1986.  The unit is regulated by  Federal TSCA
regulations  (40 CFR 761) and does not receive  hazardous waste.   Total
capacity of the unit is 150,000 cubic yards or about 93 acre-feet.

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35

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                                                                     37
      The landfill was constructed so that all waste is buried above grade. The
design is  similar to landfill cell 2, however cell X has a 3-foot compacted clay
liner. Most of the waste for cell X comes from PPM, Inc. and includes PCS
solids, transformers and debris.  During the Task Force inspection, this unit was
in service.

      Industrial Waste Landfill Cell

      The industrial waste  landfill cell is located near the northwest corner of
the Grassy Mountain facility.  The unit was built in 1985  and began accepting
waste in August 1985.  The unit is regulated by  Utah Solid Waste Regulations
and does  not accept hazardous waste.  Non-PCB transformers, empty drums,
debris and other non-RCRA waste are landfilled in this unit.   No municipal
waste has been accepted to date, but would be if a customer desired.  The
rectangular cell has finished bottom dimensions of approximately 150 feet by
1,050 feet.  The cell has a single liner and two sumps for collection of fluids.
During the Task Force  inspection, the unit was in service  and UDH inspections
indicated there was a lot of fluid in this landfill.

Tanks

      USPCI operates nine tanks for storage and treatment of RCRA waste.
PPM, Inc. operates another seven tanks for storage and treatment of PCBs at
the Grassy Mountain facility. The RCRA tanks are within the processing area
and surrounded by a clay containment dike. Any leakage from the tanks, piping
and waste transfer operations is collected in runoff control  ponds (oil/caustic
storage tanks) or sumps (solvent tanks, acid tank and reaction tank). Tank pads
are  either compacted  clay or concrete.   The  processing  area has natural
underlying silty clay soil. The PCS tanks are within a smaller separate area with
a  clay containment dike.  Any leakage from  the three storage and  three
treatment  tanks, piping and waste transfer operations is collected in sumps on
the- concrete tank pads.  The one "clean"  tank for treated oil  (sold offsite) is
located off the concrete pads.  A list of existing RCRA tanks, capacity and types
of waste stored is presented in Table 5.

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                                                                         38
                                 Table 5
   EXISTING RCRA TANKS, CAPACITY AND TYPES OF WASTE STORED*
                 Number of                 Type/Construction     Capacity
Tank Name       Tanks     Dimensions       Materials        (Gallons)
Waste oil/caustic
storage tanks
(Tanks 1-5)
                       12'Dx20'H
VA/C.S
Note:
According to the RCRA Part B permit application
Calculated from dimensions listed on design drawings

D = Diameter
H= Height
VA ป Vertical above ground
HA = Horizontal above ground
VACB = Vertical above ground with cone bottom   .
C.S. = Carbon steel
FRP = Fiberglass reinforced plastic
16,000 ea
Waste solvent 2
storage tanks
(Tanks ST1 and
ST2)
Acid waste 1
storage tanks
Neutralization/ 1
reaction tank

8'Dx21'H
10'D x 33'H


10'Dx 16'H

12'Dx20'H


HA/C.S.



VA/FRP

VACB/C.S.
with epoxy
liner
7,500
18,000**


10,000

16,000



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                                                                     39

 Drum Storage Area

      The drum storage area consists of two pads with interconnnected curbs.
 One pad has a partial roof. The pads are 2400- and 7200-square-feet and were
 built in 1982 and 1985, respectively.  The pads have 8-inch curbs and concrete
 floors, which slope to concrete sumps.  The RCRA Part B application lists the
 capacity of the pads at 250 and 800 55-gallon drums.

 Land Treatment Areas

      USPCI operates four  land treatment areas for treatment  of oily waste
 sludges from petroleum refineries and other industries. The four land treatment
 areas are designated Areas I through IV and have surface areas of 41,  68, 57
 and 40  acres, respectively.  A 2-foot dike surrounds the entire land treatment
 portion  of the Grassy  Mountain facility.   USPCI installed lysimeters  in the
 unsaturated  zone to monitor  soil moisture and four monitoring wells to monitor
 ground water.  USPCI also collects soil cores to monitor leaching from the land
 treatment area.

 FACILITY OPERATIONS

      Task Force personnel reviewed records of facility operations to identify
 any activities that might  result  in  waste releases  to  ground water.   Pre-
 acceptance  records were evaluated  to  determine how adequately  waste
 constituents have been identified in incoming waste loads.  Waste tracking
 records  were evaluated to determine how wastes were  handled and whether
 waste disposal locations have been properly recorded. These records required
 by both State and Federal interim  status regulations enable identification of
 hazardous waste constituents that could potentially be released from individual
waste handling units.
Surface Impoundment

      Two waste streams from  petroleum refineries are stored in the USPCI
surface impoundment prior to land treatment. Oil is periodically pumped off the
top of the surface impoundment.  Stored waste is pumped to a spreader prior to

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                                                                     40
land treatment.  Freeboard reference marks for the surface impoundment are on
the  pump  track  on the inner face of the surface impoundment.   As of
December 31, 1985, the surface impoundment was about half full, containing
about  1 million gallons of waste.  During the Task Force inspection, the
impoundment still  appeared to be about half full.

Landfills

      The  present grid system for locating where hazardous waste is buried
began about June 1984. Large maps of the grid system are on the hall walls in
the office/lab building.  The drum dock supervisor  provides coordinates for
buried  drums.  Lab  personnel  and landfill operators cooperate in providing
coordinates for bulk loads.

      Waste containing any free liquids is solidified prior to landfilling.  USPCI
has used oil field  mud tanks,  cement mixers and currently  uses gondola cars
(like a large dumpster or roll-off box) to mix waste and absorbent material prior
to landfilling.  USPCI switched to using gondola cars as mix tanks after the
State complained  in a November 14, 1985 memo that cement mixers did not
meet RCRA definition of a tank.

      Normally, USPCI uses solidified material and bulk  solids  for packing
around drums in the progressive slope or ramp method of landfilling used at the
site. With a large  contract to landfill over 76,000 drums, USPCI contracted with
another firm to provide a lime slurry to fill spaces  around the drums.  Old
solidification tanks were used as forms for the lime slurry.

Tanks

      Waste is directed to tanks based on the type of waste. Oil  and caustic
liquid waste is usually placed in tanks 1  through 5 with caustic waste usually
placed in tank 5 and sometimes in tanks 3 and 4.  Oil field wastes for land
treatment are usually stored in tanks 1  through  4 or the surface impoundment.
Acid waste  is stored in the acid tank and mixed  solvent waste is usually stored
in the solvent tanks (tanks  ST1 and ST2). Solvents are usually shipped offsite
for fuel blending.  The reaction tank is used for neutralization of acids/bases and

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                                                                     41
treatment of sulfides.   Freeboard in the oil and caustic tanks is  manually
measured with a tape measure once a day and after loads are pumped to the
tanks.  The solvent tanks are measured before and after each load.  The acid
and reaction tanks are not measured directly but a log of specific gravity and
volumes received is kept.

      USPCI claims not to have ever had a major spill and that any small spills
or leaks were cleaned up and the debris landfilled.  The State did order USPCI
to fix one tank that had settling problems and USPCI complied.

Drum Storage Area

      Drummed waste is off-loaded directly to the drum storage area after the
manifest has been checked, a piece count made and manifest  information
logged into the computer. The drums are sampled after off-loading at the drum
storage area. Normally, more than 20% of the drums from each waste stream
are sampled.  Each  drum is checked for free  liquids and volume of waste.
Disposition of each drum is recorded on drum disposal logs.

      The drum storage area is loosely organized and no  attempt is made to
assign a specific location to each drum.  Flammable liquids are kept on the
covered drum dock,  thus providing shade  for these drums.   Caustics and
organics are stored on one side of the drum pad and acids are stored on the
other as a method of keeping incompatibles separated.

      Acids can be pumped directly to the acid tank. Caustics and solvents are
usually transferred to their respective tanks via a tractor-pulled spreader tank.
Solids and drums containing liquids to be solidified are transferred to the landfill
via front-end loader.  Large volumes of liquids may occasionally  be pumped to
a USPCI tanker truck for transfer to the designated tank.

      Material accumulating in the drum storage area sumps is analyzed for
organic chlorides  and usually solidified and landfilled.  Records indicate no
previous incidents resulting in potential ground-water contamination from
operation of the drum  storage area.

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                                                                     42

Land Treatment Areas

      Oily waste sludges from  petroleum refineries and other industries are
applied to land treatment areas by a tractor-pulled spreader. Solids are usually
applied to area 1 by a paddle wheel cart similar to home grass seed or fertilizer
spreaders, only much larger.  Unless there is a concern about concentration,
most applications are sequential (e.g., row  1, then row  2, then row 3).   A
computer program is used to keep track of amounts applied and cumulative
concentrations of oil and metals.

      Wastes have been applied to the treatment areas since April 1982.
Wastes  destined  for  land  treatment are  usually placed  in the surface
impoundment or tanks 1 through 4 prior to application.  Gravity separation of oil
is accomplished in the surface impoundment or tanks. Oil is reclaimed from the
tanks/surface impoundments as possible.  The USPCI RCRA Part B permit
application specifies the  oil content of the  residues for  land application  is
generally 15% by weight or lower. The residue is pumped to the spreader and
applied to the designated  row and tilled into  the top 7 to 8 inches of soil.   A
spring tooth type tiller is  used  to reduce fines and blowing  dust.  The land
treatment areas are  retilled periodically to aerate the soil and promote microbial
action on the oily waste.

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                                                                     43

                         SITE HYDROGEOLOGY

      The USPCI Grassy Mountain Facility lies in the Northern Great Salt Lake
Desert in northwest Utah.  The Great Salt Lake Desert has been the subject of
numerous regional geologic and hydrologic investigations done by universities,
the State of Utah and the United States Geological Survey.  In addition, USPCI
has initiated onsite geotechnical investigations at the Grassy Mountain facility to
characterize the site hydrogeology.  These investigations primarily have been
done by USPCI consultants, Vaughn Hansen and Associates of Salt Lake City,
Utah and Chen and Associates of Denver,  Colorado.  The  investigations
include exploratory drilling,  geologic coring,  lineament  analysis, seismic
studies, aquifer testing and water level analysis.

      During  the   inspection,  Task  Force   personnel  interviewed  a
representative of Vaughn  Hansen and Associates regarding a  hydrogeologic
characterization report prepared by his firm, which was submitted by USPCI to
the State and EPA in May 1986.*  This report was prepared, as required by UDH
for the Part B application.  The following information is largely derived from the
interview and the report.

      Salt flats, lake beds of the former Lake Bonneville, alluvial material
(stream deposits)  from surrounding mountains and wind-blown sand compose
the sediments of the Great Salt Lake Desert.  At the USPCI site, the exposed
sediments are Pleistocene Lake Bonneville and younger sediments.  These
sediments consist of calcareous (calcium carbonate) clays, silts and fine to
medium-grained sands.  The lakebed sediments are more than 300 feet thick
beneath the Grassy Mountain Facility.  The  Grayback Hills are east of  the
facility. Alluvial deposits from the Grayback Hills  coalesce with the younger
lakebed sediments at the base of the Hills.  At the western edge of the site, wind
action has formed sand dunes on the surface near some topographic low spots
hereafter referred to as mudflats.  These sediment features may affect local
ground-water flow patterns.
     USPCI, May 1986.  "Response to Federal Ground Water Regulations 40 CFR 270.14(c)
     Regarding Grassy Mountain Facility Near Knolls, Utah," Volumes 1 through 3.

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                                                                     44
      Geologic core analyses on two 100-foot and one 300-foot exploratory
borings indicate that quartz and calcareous sands compose most of the layered
sands and silts  beneath the ground surface.  The May 1986 hydrogeologic
report details each of the sands, silts and clays and the original depositional
environments (e.g., open fresh water, shallow fresh water, saline shallow or
shoreline or paleosoil).

      Subsurface profiles, developed from geologic coring information indicate
the upper silty sand (dune) deposits are not continuous across the site. Various
subsurface  profiles developed  from drilling logs suggest that some of the
deeper sand units do appear to  be continuous or nearly continuous across the
site, while other units appear to be  discontinuous.   The continuous  materials
exhibit a slightly westward dip in slope. Some of these layered  units apparently
undergo gradational grain-size and compositional  changes  as  they extend
across the site.

HYDROGEOLOGIC UNITS

      The  upper 25 feet of the deposits contain  an unconfined,  principal
aquifer, known as the shallow brine aquifer.  The elevation of the water table in
the shallow brine aquifer was about  4,229 to 4,233 feet above mean  sea level
at the time of the Task Force inspection.  Depth to ground water beneath the
facility ranged from about 10 to 30 feet from  land  surface, depending upon
surface topography.

      USPCI consultants state  that the  shallow brine aquifer contains  many
dessication cracks that may be up to 1 inch in width, as close  as  1 foot  apart,
and as deep as 25 feet. The consultants contend that these cracks substantially
increase hydraulic conductivity within the aquifer and increase its water yield.
The  hydraulic conductivity and water yield in the  shallow  brine aquifer are
greater through the dessication cracks than in the underlying sediments that do
not contain cracks.  The consultants state the  increased hydraulic conductivity
as the reason this aquifer is identified as the "uppermost aquifer" for regulatory
purposes. Below the upper 25 feet, the dessication  cracks are absent or less
prevalent, thus, they are less a factor in water movement.

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                                                                      45
      The May 1986 hydrogeologic characterization report states that regional
recharge to  the shallow brine aquifer occurs primarily through lateral ground-
water flow from adjacent sediments near the Grayback Hills and upward flow
from deeper sediments.  To a much lesser extent, recharge may occur through
infiltration from precipitation and storm runoff.

      The sediments below the shallow brine aquifer have poor water yield
and variable water quality depending upon the chemical composition  of the
depositional  layer, the original depositional  environment  and  patterns of
ground-water discharge.  USPCI personnel measured specific conductance
values on the order of 90,000 to 100,000 micromhos per centimeter (jimhos/cm)
during the July 1986 sampling.  None of this ground water is used as a drinking
water supply, and it has not been classified under the Safe  Drinking Water Act.*

GROUND-WATER FLOW DIRECTION AND RATES

      The hydraulic gradient in the shallow brine aquifer across the site has a
very shallow apparent slope to the  west." Ground water flows westward from
the Grayback Hills toward the sand dunes and mudflats.  Consultants'
piezometric (water level) contour data indicate that in the vicinity  of the sand
dunes (located just east of the western mudflats) the gradient in  the shallow
brine  aquifer steepens  as ground water flows beneath the dunes  toward a
western mudflat.   Near the Grassy Mountain Facility, the flow direction diverges
toward each of three major depressional mudflats located to the south, west and
northwest of the facility.  Historical piezometric data  suggest that locally there is
decreasing hydraulic head with depth (net downward flow) beneath the facility
and increasing head with depth (net upward flow) beneath  the sand dunes and
western mudflats.

      USPCI consultants' estimation of  ground-water flow  velocity may  be
lower than the actual ground-water flow velocities as a result  of overestimating
porosity. They report the rate of ground-water flow  across the site to be about
     The Safe Drinking Water Act (42 U.S.C.A. ง 300f et seq.) defines an underground source
     of drinking water to be an underground water which  supplies or can reasonably be
     expected to supply any public water system.
     Based on June 1986 measured water levels (see Figure 6).

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                                                                     46
0.6 feet per year.* The formula used by the consultants to compute ground-
water flow velocity was:

                        V = KL where
                           n
                        V = velocity of ground-water flow
                        K = hydraulic conductivity
                        I = hydraulic gradient
                        n = porosity of the porous media

      The  consultants used porosity  values of 30% and 66%,  water level
contours developed in January 1986 for the  hydraulic gradient, and values for
hydraulic conductivity from field and laboratory testing.  The porosity values of
30% and 66% are within  published  porosity ranges for sands and clays
[Table 6].

                                Table 6
                         RANGE OF VALUES OF
                             POROSITY IN
                    UNCONSOLIDATED SEDIMENTS*
                                         Porosity n(%
                  Gravel                    25-40
                  Sand                     25-50
                  Silt                       35-50
                  Clay                      40-70
                      Source: Freeze and Cherry, 1979

      The consultants values used for computing ground-water flow velocity
are presented in Table 7.  The 66% used to compute the flow rate of about 0.3
feet per year is too high because it represents total porosity, not all of which
would  be  available for fluid  flow.   Using  total  porosity  results  in an
underestimated value for ground-water flow velocity.
    May 1986 Hydrogeologic Characterization Report

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                                                                       47
                                 Table 7
              GROUND-WATER FLOW VELOCITY COMPUTED
                        BY USPCI CONSULTANTS
K ft./sec.
4.1 x10'5
4.1 x10"5
l%
0.014
0.014
n%
30
66
V ft/year
.6
.27
      Several qualifiers apply to the computation in Table 7.  First, the K value
used is the average of K values measured in six wells, some of which are nearly
a mile apart. Second, the K values were derived from  single-hole slug tests in
each well and at best, represent ground-water conditions within a few feet of the
well tested  rather than over a broad area.  Third, a  steeper  gradient would
increase flow velocity. The Task Force computed a range of hydraulic gradients
from 0.02 to 0.29%, using June 1986 water level data. A gradient as high as
0.2% would increase the computed flow velocities to about 9 and 4 feet per year
for values of n =  .3 and n  = .66, respectively. Additionally, the desiccation
cracks in the shallow brine aquifer and any  sand lenses in the sediments would
be  preferential  ground-water flow paths. The May 1986 hydrogeologic report
does not calculate ground-water flow velocity using the effective  porosity of
sand (i.e., a lower value of porosity that represents a volume of void space
actually available for ground-water flow).' For all these reasons,  the Task Force
believes ground-water flow velocity at Grassy  Mountain could range up to one
and perhaps two orders of magnitude above the values in Table  7.

      The loading activities of building  the berms surrounding landfill cells 1
and 2  and filling the cells with waste  materials appear to have altered  the
ground-water flow patterns in the vicinity  of these disposal units.  Consultants to
USPCI state that the  loading at the surface has caused sediment compaction
immediately beneath the landfill cells, so that the dessication cracks seal under
the weight and no longer serve as primary avenues of ground-water flow.  As a
     Some void space in earth materials is occupied by air and fluids held by surface tension.
     This void space is unavailable for transmitting fluids and should be subtracted from the
     porosity (total void space) value, leaving an estimate of what is known as "effective porosity"
     (i.e., that pore space in earth materials capable of transmitting fluids).

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                                                                     48
result, sediment permeability beneath the cells decreases.  The Task Force
agrees with this conclusion.

      The loading of the landfill cells and resultant compaction has caused a
rise  in ground-water pore  pressure  beneath the cells.  USPCI consultants
contend that the rise in pore pressure is indicated by unusually high ground-
water levels in the vicinity of the cells and normal levels elsewhere on the site.
The  effect of elevating the water table  is the induction of a slightly steeper
hydraulic gradient around the cells (i.e., a ground-water mounding effect). The
"mounding" should not affect background wells at USPCI because the effect is
slight and the background wells are  several thousand feet away.  The Task
Force agrees that this effect should equilibrate and a shallow gradient should
be restored once surface loading has ceased.

      USPCI needs to  survey the monitoring wells regularly to provide a basis
for reliable water level measurements. The very shallow gradient necessitates
careful piezometric analysis.  The Task Force was unable  to  verify that water
levels in monitoring wells MW-13 through MW-17 might  be unusually high
because these wells, constructed in the landfill berm, had settled and had not
been resurveyed.  Consequently, the accuracy of water levels measured in
these wells is questionable.  Water level elevations measured  by the Company
during the Task Force inspection appear in Figure 7.

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                                                               49
             M W • 7
             4229.4
        ACCESS RCAO,
                        M W • 1 4 H
                                    MW-ll .
                              4233.3   4232.2
                      4233.2

                        MW-I5
                      4233.6 ,

                        MW-16 !•
                      4233.4
                        MW-17
                      4233.1
                                M W • 3
                                4232.6
MW-9 •!
4233.0
                       LAND TREATUENT AREA II
                                               IANO TREATUENT ABEA I
                                                            MW-20 •
                                                              423Z.7
                        LAND TREATUENT AREA III
Approximate Scale
                                              LAHO TREATMENT AREA IV
600

300
M o n i t
0
o r i ng
600
Well
Feet \ , '
MW/8 MW-1
4231,4 4232.7 •
           Figure 7.  Water  Level Elevations
                     (feet above mean sea level)
                             June  1986

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                                                                    50

   GROUND-WATER MONITORING PROGRAM DURING INTERIM STATUS

      This section is an evaluation of the interim status monitoring program at
Grassy  Mountain between March  1982 and June 1986, the time of the Task
Force inspection.  Table 8 presents a brief regulatory history with  respect to
ground-water monitoring. The section also addresses the following topics:

      Regulatory requirements
      Ground-water sampling and  analysis plan
      Monitoring wells
      Sample collection and  handling procedures
•     Ground-water Quality Assessment Program

      Prior to 1986, the effort to collect background ground-water quality data
identified continual problems  stemming from the inadequacies in sampling and
analysis, the  nature of the saline aquifer, and the inappropriateness of certain
analytical methods for saline ground-water samples.  UDH had to re-evaluate
the background water quality characterization  several times in  the period
between 1982 and 1986 in an effort to obtain reliable ground-water quality data.

      In 1983, UDH determined that previous ground-water quality analyses for
the Grassy Mountain facility did not accurately depict background water quality
conditions.  UDH ordered the data collection for background water quality to be
restarted. The continuing effort to obtain meaningful background data  resulted
in quarterly monitoring at Grassy Mountain through  the end of 1985.  In 1986,
USPCI  began a new period of data collection for background water quality
comparisons using additional wells.*

      As a result of triggering ground-water assessment under UHWR 7.13.4
(40 CFR 265.93) in October 1985, the Grassy Mountain Facility also began
quarterly assessment monitoring during the first quarter of 1986.  EPA and UDH
requested that  USPCI  analyze for organic  parameters  in addition to those
    Phone conversation with Roy Murphy, USPCI, February 11, 1987

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                                                                                 51
                                     Table 8

   REGULATORY AUTHORITY, REQUIREMENTS AND EVENTS DURING INTERIM STATUS
    Date
                           Action
December 1980




March 1982

1983
September 1984



Februarys, 1985




March 5,1985




June 19, 1985


October 2, 1985




October 21, 1985



October 31, 1985


Novembers, 1985

November 13, 1985
Utah received RCRA interim authorization.

The Utah Hazardous Waste Rules (UHWR) became effective Decem-
ber^,  1980.

Grassy Mountain Facility began waste management activities.

Utah Department of Health (UDH) determined that previous ground-water
analyses for the Grassy Mountain Facility did  not accurately depict
background water quality conditions.

UDH ordered the  data collection for background water quality to be
restarted.

Utah received final RCRA authorization, with exception of authorization
for the Hazardous and Solid Waste Amendments of 1984 (HSWA).  EPA
administers HSWA in Utah.

UDH issued a Notice of Violation (NOV) and  Order of Compliance
(NOV/CO No. UTD9931301748) citing USPCI for having inadequate
placement of monitoring wells and for not having an acceptable sampling
and analysis plan.

USPCI agreed to: (1) prepare a hydrogeologic  survey at the site, (2)
locate new monitoring wells, (3) establish new ground-water monitoring
procedures and (4) provide employee training on implementing the
ground-water monitoring procedures.

USPCI submitted a proposed plan for the hydrogeologic investigation to
EPA.

UDH and USPCI signed a Stipulation and Consent Order in which USPCI
was ordered to install a mutually-agreed-upon ground-water monitoring
system  and develop  and follow  a sampling  and analysis plan by
Novembers, 1985.

EPA notified UDH that total organic carbon (TOC) in well MW-3 showed a
statistically significant increase. EPA determined that USPCI should be in
assessment monitoring under UHWR 7.13 (40 CFR Part 265.93).

UDH told USPCI  to submit a water  quality assessment monitoring
program.

USPCI submitted a sampling and analysis plan to UDH.

USPCI notified UDH that the Grassy Mountain facility would enter ground-
water assessment monitoring in conjunction with the sampling  and
analysis plan.

UDH formally requested the (overdue)1 assessment plan. USPCI did not
submit the plan.

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                                                                                     52
                                     Table 8 (cont.)

   REGULATORY AUTHORITY, REQUIREMENTS AND EVENTS DURING INTERIM STATUS
    Date
                                                  Action
January 1986


February 21, 1986
                      USPCI restarted background ground-water quality monitoring, including
                      newly-installed monitoring wells (MW-9 through MW-20).2

                      UDH requested the assessment plan again.

                      UDH also identified certain information  related to ground water that
                      should have been forthcoming in USPCI's Part B resubmission due in
                      late March 1986.  This information was specifically described in a letter
                      from EPA to UDH dated February 4,1986.

                      USPCI submitted a hydrogeologic  characterization report on  Grassy
                      Mountain Facility.3 USPCI still had not submitted an assessment plan, as
                      required by UHWR7.13.4.4

1      UHWR 7.13.4 (40 CFR 265.93) requires that the owner/operator develop and submit an assessment
       plan within 15 days of notifying the regulatory authority of a statistically significant increase in
       indicator parameters.
2      Phone conversation with Roy Murphy, USPCI, February 11, 1987.
3      USPCI, May 1986, "Response to Federal Ground-Water Regulations, 40 CFR 270.14(c), Regarding
       Grassy Mountain Facility Near Knolls, Utah,'Volume 1-3.
4      EPA and Utah State Regulations are cross-referenced in Table 8.
May 1986

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                                                                 53
parameters required by UHWR 7.13.3 (40 CFR 265.92).  The 1986 quarterly
sampling parameters appear later in this report in a section entitled, "USPCI
Sample Collection and Handling Procedures."

      Also in early 1986,  USPCI began sampling a number of new monitoring
wells installed in response to an October 1985 Stipulation and Consent Order
from UDH.  The existence of these  new wells is one reason USPCI restarted
background water quality monitoring  in  1986.

      EPA  and UDH agreed to allow USPCI  to submit the results of the
hydrogeologic investigation as late as March 1986, so that  USPCI could
concentrate on installing monitoring  wells in order to  meet a  statutory
Novembers, 1985 deadline for certifying ground-water compliance  under 40
CFR Part 265.  USPCI submitted the hydrogeologic characterization report to
UDH in May 1986.

REGULATORY REQUIREMENTS

      The State interim status ground-water monitoring requirements (UHWR
7.13) are equivalent to the RCRA interim status requirements contained in 40
CFR Part 265, Subpart F; there are no substantive differences.  Regulation
counterparts are shown in  Table 9.

                              Table 9
                STATE AND FEDERAL COUNTERPART
                INTERIM STATUS REGULATIONS (1986)

                                              RCRA Regulation
      Subpart Title*                    UHWR        (40 CFR Part)
Applicability
Ground-Water Monitoring System
Sampling and Analysis
Preparation, Evaluation and
Response
Recordkeeping and Reporting
7.13.1
7.13.2
7.13.3
7.13.4
7.13.5
265.90
265.91
265.92
265.93
265.94
           Subpart titles are the same in both the State and RCRA regulations.

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                                                                   54

GROUND-WATER SAMPLING AND ANALYSIS PLAN

      This section evaluates the completeness and adequacy of the USPCI
sampling and analysis plan.  USPCI is required  by interim status regulations in
UHWR 7.13.3 (40 CFR 265.92) to develop and follow a sampling and analysis
plan. This plan must contain procedures  and techniques for:  (1) sample
collection, (2) sample preservation and shipment, (3) analytical procedures and
(4) chain-of-custody control.

      Prior to November 1985, USPCI did not have an interim status ground-
water sampling and analysis plan at the Grassy Mountain facility, as required by
UHWR 7.13.3. Prior to November 1985, USPCI had submitted a sampling and
analysis plan with their Part B Application to UDH and EPA.  Both agencies
determined that the submitted plan was deficient and did not meet regulatory
requirements for either  interim status or the  permit.  USPCI submitted a
November 1985 plan (the plan) to UDH and EPA in  response to the October
1985 Stipulation and Consent Order issued by UDH.  Company personnel told
the Task Force that this  November plan was the interim status sampling and
analysis plan.

      USPCI personnel also told the Task Force that they first used  the
November 1985 plan the first quarter of  1986.   However, the individual
responsible for sampling at the Grassy Mountain Facility during the first and
second quarters of 1986, told Task Force personnel he  had  not seen that plan
until commencement of the Task Force inspection (June 1986). No plan had
been used at Grassy Mountain prior to that.

Elements of the USPCI Sampling and  Analysis Plan

      The November 1985 sampling and analysis plan contains procedures for
the following elerrrentsr---	

      Measuring depth to water
      Well evacuation
      Sample collection and field measurements
      Collecting field blanks

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                                                                      55
      Preservatives
      Analytical procedures, including laboratory quality assurance and
      quality control
      Chain-of-custody
•     Shipping

      The methods in the plan for measuring static water levels are acceptable
except for the provision that measurement accuracy be obtained within 1/32 of
an inch (about 0.003 feet).  This accuracy is unrealistic and cannot be obtained
with the electric water level indicator used by the facility.  A more obtainable
value is 0.01 foot with a steel tape  or 0.1 foot with an electric tape.

      Methods in the plan for purging the well are acceptable except for the
example calculation on how to calculate purge volumes.  This calculation is
incorrect in that it indicates a 2-inch (inside diameter) pipe holds 11  milliliters
(ml) of water per inch length of pipe. The correct volume is approximately 51  ml
per inch.

      The example table in the plan showing volume of water in MW-8 per inch
of water column needs to be removed or corrected to reflect accurate numbers.
If the table is retained, the total depth of MW-8 should appear so that total water-
column volume may be calculated.   Furthermore, using well MW-8 as an
example for calculating purge volumes is inappropriate, as USPCI no longer
samples this well.

      The methods in the plan  for field sampling are acceptable,  with the
exception of waiting until all the wells are purged before sampling begins.  At
the Grassy Mountain facility, purging  all the wells takes  24 hours  or more.
Although some lag  time  may be necessary for slowly recharging wells, those
that recharge quickly should be sampled as soon as possible in order  to obtain
as fresh a sample from the aquifer as  possible. Allowing water in the well to
recharge, stagnate and  have prolonged contact time with air and  the  well
casing needs to be avoided so that the sample is representative of the quality of
water flowing  through the aquifer.

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                                                                     56
      The provisions in the plan for field blanks need to include instructions
that blanks for sample parameters that are preserved in the field be preserved
in the same manner.  Otherwise the method for field blanks is acceptable.

      The provisions in the  plan  for preservatives, chain-of-custody and
shipping are also acceptable.

      The plan includes a four-page, unreferenced  list of  Appendix VIII
compounds.  Laboratory* personnel were unable to  explain the source of this
list  or the  reason for it in the plan.  The laboratory does not analyze for each of
the parameters listed, neither does the plan indicate which of these parameters
the laboratory does analyze. Only the list of compounds actually analyzed for
should appear in the  sampling and analysis plan.

      The plan does not  list appropriate analytical methods for specific organic
analyses to be done.  Only one analytical method for each compound should be
listed in the plan and only  that method should be followed, thereby allowing
statistical comparison of analytical data.

      The plan does not  identify appropriate detection limits for  all compounds
which NAL is capable of achieving.  Appropriate, achievable detection limits
need to be presented.

Sampling  Records Purina Interim Status

      USPCI did not follow the November  1985 sampling and analysis plan
with respect to sampling  records  in 1986.   USPCI began keeping more
thorough sampling records beginning with the first quarter of 1986, although not
all of the sampling activities were done for every monitoring well.  Task Force
personnel were able to verify that water level measurements, quarterly
sampling,  replicate field  measurements and wellhead inspections  had been
done during the first and second quarters of 1986, but not at every well for each
sampling.  Most of the field procedures were consistent with the 1985 sampling
and analysis plan, even though  the sampler had not seen that plan.
     National Analytical Laboratories (NAL), Tulsa, Oklahoma.

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                                                                  57
      The sampling and analysis plan states that 19 monitoring wells (MW-1
through MW-7, MW-9 through MW-20) would be sampled quarterly for 1 year,
beginning with the first quarter of 1986; however, field records for 1986 do not
show that all 19 wells were sampled according to the prescribed schedule.
USPCI no longer samples MW-4.  Sampling records indicate that MW-7 and
MW-6 were not sampled in the second quarter of 1986.  USPCI indicated MW-7
would not have been sampled in June 1986 had the Task Force not selected it
for sampling (USPCI credited split samples from the June Task Force inspection
toward their third quarter sampling  event).  MW-3 was physically removed in
August 1986 and replaced with a new well, MW-26.

      The sampling and analysis plan also states that USPCI would measure
water  levels  in the  monitoring wells each  month for  1  year, beginning
December 1,  1985.  Field sampling records for December 1985 and the first
half of 1986 do not indicate that USPCI measured all the water levels according
to the prescribed schedule [Table 10].

                              Table 10
               WATER LEVEL MEASUREMENTS OMITTED
                      December  1985 - June 1986
            Year        Month                Well

            1985       December     MW-1 through MW6,
                                     MW-16, MW-18, MW19
            1986       January        MW-9 through MW12,
                                     MW-17 through MW-20

                       March         All Wells
      Prior to the implementation of the interim status sampling and analysis
plan in 1986, a few scattered and incomplete sampling records were found in
Company  files,  but no complete continuous sampling records were  found.
USPCI indicated that several individuals had been doing the sampling and that
there had been no continuity of personnel responsible for sampling.  Company

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                                                                    58
 records reflected this situation. As a result of this poor documentation, the Task
 Force was unable to verify the field sampling  procedures prior to 1986 for the
 purpose of determining regulatory compliance.  Records of analysis and water
 surface elevations  required  by  UHWR 7.13.3 (40 CFR 265.92)  must be
 maintained for compliance with UHWR 7.13.5 (40 CFR 265.94).

 MONITORING WELLS

      At the beginning of the inspection, USPCI personnel indicated which
 wells at Grassy Mountain were  included in the interim status  ground-water
 monitoring system.  The monitoring system was evaluated for well construction
 and for numbers and locations of wells.  Well construction for newer wells was
 determined to be acceptable, whereas, the complete construction details for
 older wells could not be determined due to insufficient information. Placement
 of some of the older wells was not satisfactory.  The selected locations of newer
 wells MW-9 through MW-20 are satisfactory.  These issues are discussed  later
 in this section.

      Evaluation  of  well  construction  included determining  whether
 construction  materials  and well design met regulatory requirements in UHWR
 7.13.2 (40 CFR 265.91).   Evaluation of well  locations included determining
 whether or not the monitoring system met requirements of UHWR 7.13.2.

      At the time  of  the inspection, USPCI  personnel  could not  identify
 precisely  which wells were  included  in the interim  status ground-water
 monitoring program and  which  wells were being used for  other purposes.
 USPCI changed the list  of wells they sample from those  identified in the
 November 1985 sampling  and analysis plan.  The sampling and  analysis  plan
 needs to be updated to reflect any changes  and USPCI needs to notify the
 State of  any well additions or deletions.   The USPCI hydrogeologic
characterization report, submitted in May 1986, indicates that older wells MW-4,
 MW-6, MW-7 and MW-8  are  no  longer used  for ground-water  sampling but
 serve only to monitor piezometric surfaces.  USPCI personnel indicated  that
only  MW-4 and  MW-8 are no longer sampled but did not say why.*   The
     Telephone communication with Lee O'Laughlin, USPCI, Novembers, 1986.

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                                                                    59
November 1985 sampling and analysis plan states that USPCI samples MW-4,
MW-6 and MW-7. USPCI needs to clarify these discrepancies and notify UDH
of which wells are included in interim status ground-water monitoring.

      The entire ground-water monitoring system at the  Grassy Mountain
Facility  consisted of 23 completed monitoring  wells, designated as MW-1
through MW-23 [Table 11, Figure 8].  MW-1 through MW-8 were completed in
1981 and, until the first quarter of 1986, served as the only RCRA monitoring
wells. USPCI ceased sampling MW-8 during the fourth quarter of 1985. MW-9
through MW-20 were completed  in late 1985 and  became  part of the RCRA
interim status monitoring system starting the first quarter of 1986.

      In 1986, wells MW-21 through MW-23 were drilled in order to monitor the
PCB landfill X regulated by the Toxic Substances and Control Act (TSCA) and
EPA. USPCI samples MW-21 through MW-23 as part of  the interim status
monitoring program.  Also in 1986, the State requested USPCI to install MW-24
and MW-25 at specific locations east of landfill cell 2 in order to confirm or refute
the suspicion that landfill cell 2 was leaking.  MW-24 and MW-25 were not in
service in time for the Task Force inspection (June 1986).

Well Construction

      The driller's construction summary is insufficient to determine that the old
monitoring wells,  MW-1  through MW-7, were  properly  constructed  for
compliance with UHWR 7.13.2 (40 CFR 265.91).  The construction design and
materials for the new monitoring  wells MW-9  through MW-23 are acceptable.
Information on well construction was derived primarily from the May 1986
hydrogeologic report which includes general  summary descriptions from  the
drilling company for MW-1  through MW-7 and well design and construction
specifications for MW-9 through MW-20. No construction specifications for MW-
8 were provided. Information on MW-21 through MW-25 was obtained directly
from USPCI.  Well specifications for MW-1  through MW-25 appear in Table 12.

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                                                              60
                     Table 11
 USPCI INTERIM STATUS MONITORING WELLS
                    June  1986
Well
Number
MW-1
MW-2
MW-3
MW-4*
MW-5
MW-6**
MW-7*
MW-8*
MW-9
MW-10
MW-11
MW-1 2
MW-1 3
MW-1 4
MW-1 5
MW-1 6
MW-1 7
MW-1 8
MW-1 9
MW-20
MW-21*"
MW-22***
MW-23***
USPCI
Designation
Upgradient
Upgradient
Downgradient
Downgradient
Downgradient

Downgradient
Downgradient
Upgradient
Downgradient
Downgradient
Downgradient
Downgradient
Downgradient
Downgradient
Downgradient
Downgradient
Downgradient
Downgradient
Upgradient
Downgradient
Downgradient
Downgradient
Waste Management
Unit Monitored
Landfill cell 1

Land treatment area


Land treatment area

Surface impoundment
Surface impoundment
Surface impoundment
Landfill cell 2
Landfill cell 2
Landfill cell 2
Landfill cells 1 & 2
Landfill cell 1
Land treatment area
Land treatment area

Landfill cell X
Landfill cell X
Landfill cell X
In practice, USPCI does not sample MW-4, MW-7 and MW-8, but
measures only water levels in these wells.
MW-6 is downgradient from the land treatment area and upgradient
from the industrial landfill.

Wells MW-21, MW-22 and MW-23 monitor a PCB landfill regulated
by the Toxic Substances Control Act (TSCA), 40 CFR 761.  These
wells were sampled as part of the interim status program during the
Task Force visit.

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                                                                   61
                                          IMPOUNDMENT^

                                      r-MW-12iซ
                                                        LANOFIUl
                                                      MW-22
                                                         CELL X

                                                       MW-23
                                            CONTROL

                                              POND'
                                                          ACCESS ROAD

                                                                MW-9
                                                  LAND TREATMENT AREA I
                          LAND TREATMENT AREA II


                             A         A
                          LAND TREATMENT AREA III
                                                 ILANO TREATMENT AREA iv
  Approximate Scale

600  300  0	600 Feet


	 • Monitoring Well  A Lysimeter
    Figure 8.  Monitoring Well  and Lysimeter Locations

                               June 1986

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                                                          62
                     Table 12
CONSTRUCTION SPECIFICATIONS FOR MONITORING WELLS
            USPCI Grassy Mountain Facility
As-Built
Top of Casing
Cap Elevation
Well (ft. MSL)1
MW-1 4240.03
MW-2 4240.76
MW-3 4244.35
MW-45 4252.54
MW-5 4257.32
MW-65 4262.34
MW-75 4249.09
MW-85 4244.04
MW-9 4238.65
MW-10 4242.82
MW-11 4242.94
MW-1 2 4243.26
MW-1 3 4262.65
MW-1 4 4262.25
MW-1 5 4262.46
MW-1 6 4262.03
MW-17 4263.18
MW-1 8 4249.57
MW-1 9 4247.65
MW-20 4238.16
MW-21 4241 .76
MW-22 4241 .34
MW-23 4241 .92
MW-24
MW-25
Depth to Static Water
Water Level Elevation Total Depth
(ft.)2 (ft. MSL)3
7.3 4232.7
8.5 4232.3
1 1 .8 4232.6
20.4 4232.1
26.9 4230.4
32.8 4229.5
19.7 4229.4
1 1 .6 4232.4
5.7 4233.0
10.6 4232.2
10.7 4232.2
10.6 4232.7
29.4 4233.3
29.1 4233.2
29.0 4233.6
28.6 4233.4
30.1 4233.1
17.5 4232.1
15.6 4232.1
5.5 4232.7
9.4 4232.4
9.0 4232.3
9.6 4232.3


1 USPCI "Response to Federal Ground-Water Regulation, 40
Utah, " May 1986 submittal;
feet above mean sea level.
2 Measured on June 23 through 24, 1986 during Hazardous
0. 1 foot

Approximate
Perforated
Interval
(ft.)' (ft. to ft. MSL)
14
14
18
40
30
39
34

15.5
19.3
19.7
18.66

40.3
41 ,27
39.8
40.5
27.1 6
26.46
14.3e
18.8
18.5
18.9


CFR 270.14(c) Regarding

4236-4226
4237-4227
4236-4226
4223-4213
4237-4227
4233-4223
4225-4215

4234.4224
4234-4224
4234-4224
4234-4224
4233-4223
4233-4223
4232-4222
4233-4223
4234-4224
4231-4221
4232-4222
4235-4225
4234-4224
4234-4224
4234-4224
4234-4224
4234-4224
Grassy Mountain

Waste Ground-Water Task Force inspection;


Bottom of
Casing
Elevation
(ft. MSL)
4226.03
4226.76
4226.35
4212.54
4227.32
4223.34
4215.09

4223.15
4223.52
4223.24
4223.3
4222.1
4221 .95
4221 .26
4222.23
4222.68
4220.1
4220.6
4224.1
4223.1
4223.1
4223.1
4223.0
4223.0
Facility near Knolls,

rounded to nearest

3 Rounded to nearest 0. 1 foot
4 Source: USPCI sampling personnel's field records; May 1986 submittal
5 Piezometric levels only




6 Back calculated from water level records
7 Back calculations from water level records indicate this well is 39.6 feet deep. USPCI was unable to provide an explanaton for
this discrepancy





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                                                                      63
      The Task Force asked  for and did not receive any detailed drilling or
construction logs for monitoring wells MW-1 through MW-7.  Well completion
information from the driller's summary provided in the May 1986 hydrogeologic
report was limited to drilled depth, casing length, perforated interval, gravel
pack interval and casing materials.  According to the driller's summary, wells
MW-1 through MW-7 are each cased with 4-inch polyvinylchloride (PVC) casing
that extends approximately 2 feet above the land surface.  A 4-foot length of
8-inch steel casing  protects the PVC casing at the wellhead and  extends
approximately 2.5 feet above ground surface.  The gravel  pack around the
screen extends to a height of 2 feet above the screen.  A bentonite pellet seal
was placed in the annular space from the top of the gravel pack to ground
surface.  This information is insufficient to document compliance with UHWR
7.13.2 (40 CFR 265.91).  Additional information that is needed includes, but is
not limited to:

      •      The type and grain size distribution of the gravel pack

      •      The size of screen openings

            The casing joint fittings (i.e., are they flush-fitted screw joints, glued
            joints, etc.?)

            The total depth of the borehole

      •      Any plugged back depth of the borehole

            The borehole diameter

            The volume of gravel-pack bentonite  used and the method of
            installation
            The well development technique

      The  May  1986  hydrogeologic report states that  the general design
specifications [Figure 9] for the casings and screens of the monitoring wells
MW-9 through MW-20 are as follows (from bottom to top):

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                                                                        64
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 Figure 9.  General Monitoring  Well Construction (MVV9  through MW25)

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                                                                       65
             A 1-foot blank length of Schedule 80, 2-inch diameter of Teflon
             casing

      •      A 10-foot length  of  Schedule  80,  2-inch  diameter Teflon well
             screen with slot size of 0.01  inch

      •      A 2-foot length of Schedule 80, 2-inch diameter Teflon casing to a
             height of 1.5 feet above the  projected  high water table.  The
             projected high water  table was based upon historical piezometric
             data.

             A variable length  (depending on the well) of Schedule 80 2-inch
             diameter PVC casing  to a point above ground surface

      •      All casing/screen joints are threaded flush joints.

      USPCI placed the well screens in MW-9 through MW-20 so that the open
screen area would intersect the fluctuating water table.* The sand pack in the
annular space opposite the well  screen consists of a clean, quartz sand"
placed from the bottom of the hole to a height approximately 0.5 feet above the
well screen.  A 1- to 2-foot sodium bentonite seal was placed in the annular
space above the  sand pack, followed by cement  grout to within 2.5 feet of the
surface.  The remaining 2.5 feet of hole was enlarged and filled with cement
grout that also created a concrete apron around  the well at the surface.  This
apron both supports a  lockable  steel protective well  covering and directs
precipitation away from the well.

      USPCI provided drilling construction details for MW-21 through MW-26 to
the Task Force after the inspection. These wells are designed similarly to MW-9
through MW-20 (MW-26 was installed in August 1986).
     USPCI has noticed some settling of wells completed in the landfill berm (MW-13 through
     MW-17), so that the open screen area may no longer continuously intersect the fluctuating
     water table.
     Particle size gradation is provided in the May 1986 hydrogeologic report.

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                                                                    66

Well Locations

      The  locations  of interim status ground-water monitoring wells MW-9
through MW-25 were decided by the Company and the regulatory agencies
prior to installation.* The well locations were selected using guidance provided
in the EPA  Ground-Water Monitoring Technical  Enforcement Guidance
Document.' USPCI has not provided rationale for the locations of wells MW-1
through MW-8, however MW-1 and MW-2 provide useful background and
piezometric data.  MW-5 is useful for downgradient monitoring of  the  land
treatment areas.

      USPCI  has located  upgradient wells at  a distance from  waste
management units so that they monitor background water quality unaffected by
site activities.  This conclusion is based upon the  direction of the hydraulic
gradient in the monitored aquifer and the distance  of the upgradient wells from
waste management units.

      The Company has located three downgradient wells at the downgradient
boundary of each waste management unit.  In the cases of landfill cells 1 and 2,
the surface impoundment, and  PCB  cell  X, the  downgradient wells are
sufficiently close together (100 to 200 feet) to expect that they would intercept a
contaminant plume issuing from the waste management unit.

      The  three  wells  downgradient  from the land  treatment  area are
approximately 1,000 feet apart.  Closer spacing probably would not significantly
enhance the  capability to immediately detect a  contaminant plume.  Four
lysimeters have been  installed in each of the four land treatment areas to collect
water samples from the unsaturated zone 36 to 48 inches below ground surface
[Figure 7].  The water samples are analyzed for hazardous constituents.  The
lysimeters, together with soil cores, would detect these constituents long before
the monitoring wells.

      The 1986 hydrogeologic report provides information that suggests an
aqueous plume would move slowly  across  the land treatment area and be
    Stipulation and Consent Order between UDH and USPCI, October 2, 1985

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                                                                   67
dispersed over a broad  area  prior to  reaching the monitoring  wells.   For
instance, the natural hydraulic gradient is very low, and the resulting potential
velocity of ground-water movement is low (estimated at less than 0.1 to 10 feet
per year).  Much of the water beneath the land treatment area must travel a long
distance to reach the monitoring wells.  The land treatment area encompasses
a broad area (206 acres) and is about three quarters of a mile across from east
to west (the direction of ground-water movement).

      As  for the fate of the  contaminants, piezometric data support the
conclusion that net ground-water flow in the uppermost aquifer moves westward
toward the mudflats, with slight diversion to the southwest and northwest toward
mudflats located in those directions.  These mudflats exist where ground water
ultimately  discharges  from beneath  the land treatment area.  Some  ground
water may continue to flow beneath and beyond these mudflats.

      The remote locations of monitoring wells MW-4,  MW-6 and MW-7 render
these wells  incapable of  providing immediate leak detection from any waste
management units existing during the Task Force inspection.   These well
locations  may  eventually be useful for ground-water monitoring  or for
piezometric levels as additional waste management units become active.

USPCI SAMPLE COLLECTION AND HANDLING PROCEDURES

      During the inspection, the Task Force evaluated sample collection and
handling procedures practiced by USPCI personnel. The evaluation included
observing water level measurements,  well purging  procedures, field  data
collection,  and  sample  collection, preservation and  shipment.    USPCI
procedures were evaluated for technical  soundness and for compliance with
the  sampling and analysis plan, as required by UHWR 7.13.3 (40 CFR 265.92).
The Task Force observed that in several instances, USPCI personnel  did not
follow the sampling and analysis plan.

      The Task Force observed water level measurements during the initial
onsite visit and well purging in June 1986. At this time, samples were collected
from 10 wells by an EPA contractor but not by USPCI.  The Task Force elected
to observe routine sampling procedures by the Company during a  subsequent

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                                                                    68
site visit July 9 through 11, 1986. In July, USPCI personnel did normal quarterly
sampling at wells which had not been sampled by the Task Force in June.  This
section details procedures used by USPCI personnel during the July sampling.

      At the time of the Task Force inspection, the Company was in the process
of training personnel for the  sampling responsibility.  As a result, the  field
methods the Task Force observed during the July quarterly sampling were done
by personnel not normally responsible for those duties and by personnel being
trained for those duties.

Water Level  Measurements

      At the wellhead, the first step USPCI followed in collecting samples was
measuring depth to  water using  an electric water  level indicator (ACTAT
Olympic Well Probe, Model 150).  The water level indicator consisted of a reel
with electric cable and sensor equipped with a battery power supply and a
buzzer.  The cord had cylindrical metal weights attached below the sensor, so
that the sensor was between the cord and the weights.  There was no meter on
the instrument and contact with water was signaled solely  by  the  sensor
activating the buzzer.

      The water level  indicator used was insufficient.  Moisture in the  well
(above the water level) set off the buzzer by bridging across the sensor, thereby
closing the electrical circuit and reading false water  levels. The absence of an
ammeter on the instrument  prevented double checking  the  buzzer  and
determining  whether the reading  was a good  one.   Task Force personnel
judged the accuracy of the water level measurements to be within +0.2 feet,
based upon the repeatability of sequential measurements.

      All the USPCI wells, except MW-8,  had dedicated Well Wizard pumps,
including a wellhead assembly from which the pumps were  suspended.  The
wellhead assembly had an access port through which the water  level  sensor
and  cord were  lowered [Figure 10].   Water  levels were measured  with
reference to the  top of the cap on the top of the  well casing, which  was a
surveyed reference point.

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                                                                                                     69
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                                                                    70
      The cord,  which was  marked  in sequential  5-foot increments, was
lowered into the well until the sensor reached the water, as indicated by the
buzzer. The cord was  then slowly raised and lowered until the point at which
the sensor made contact was determined.  The cord was then marked with
chalk by the sampler adjacent to the lip of the access port, and the distance from
the chalk mark to the next higher cord marker was measured with a measuring
tape. Depth to water was calculated by subtracting the reading made with the
measuring tape from the cord marker value. Water level measurements had to
be repeated several times to ensure that electrical bridging across the  sensor
caused, for example, by humidity in the well, was not giving false readings.

      Following the measurement, the  entire length  of cord that entered the
well, the sensor and the metal weights were triple-rinsed with deionized water.
The deionized water was sprayed from a squeeze bottle with a very thin spray.
The thin spray was difficult to keep trained on the thin cord to the meter,  thus, a
triple rinse on the entire length took a long time to accomplish, and some
segments of the  cord may not have been adequately rinsed.  A more efficient
method of rinsing would ensure a better rinse.

Purging

      USPCI personnel handled all wellhead equipment and purged each well
during both the June Task Force inspection and the July quarterly sampling, as
noted earlier. Each sampled well was equipped with  a dedicated Well Wizard
bladder pump and well  head assembly.

      The power source for operating the pumps was the 12-volt battery of one
of the Company trucks  attached to the Well Wizard control box with  electrical
jumper cables.   During sampling, this  truck  with its attendant exhaust was
positioned downwind from the wellhead. For two wells, MW-15 and MW-14, a
portable generator served^as~the-powef-source because there was no access
available for the truck.

      USPCI personnel correctly determined  the volume of water in the well
casing using the measured depth to water, total well depth and casing diameter
(even though the sampling and  analysis plan provides an incorrect  method).

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                                                                    71
Total well depth data came from well construction records.  Once the volume of
the water column was calculated, USPCI personnel multiplied the volume by
three to obtain the total amount of water to be evacuated.

      Purge water was discharged into  a  graduated bucket  in order to
determine when the three water column volumes had been obtained.  As the
bucket filled, it was emptied into a large drum for subsequent disposal.

Field Data and Sample Collection

      USPCI personnel  first measured water levels in every well.  They then
purged all the wells.  Finally they began sampling.  In some cases, sampling
commenced as much as  24 or more hours after purging stopped.  This lag time
is not necessary on all wells, as many of them  recover rapidly from purging and
could be sampled immediately upon completion of purging or at least within a
few hours.  If full recovery exceeds 2 hours, the Company needs to extract-the
sample as soon  as sufficient volume  is  available for a sample for each
parameter/

      During the July quarterly sampling, USPCI personnel began sampling by
clearing the water line from the pump to the wellhead then collecting an aliquot
of sample for making field  measurements,  including temperature, specific
conductance and  pH.  USPCI had  ordered a new conductance  meter (YSIฎ
Model 32) and was using  it for the first time.

      Both the conductance meter and the pH  meter were standardized prior to
making  measurements  on sample water.  The  conductance  meter was
calibrated with standards having  specific conductance values of 24,820 and
111,900 [imhos/cm. These values are appropriate  for the naturally high total
dissolved solids (TDS)  in ground  water  at  this site.  The pH meter was
calibrated with standards  having pHs in the range of 7.4 and 10.4.
     TEGD
     YSI is a registered trademark and will be shown hereafter without the ฎ.

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                                                                     72
       For pH, the 7.4 standard was run first, then the 10.4 standard was run.
 The samplers did not return to the 7.4 range to double check that the instrument
 had not drifted after adjustment to 10.4. Since the ground water beneath the
 USPCI site typically has a pH around 7.1 to 7.5, the 7.4 standard should have
 been rechecked following the 10.4 standard.

       Four replicate  measurements were  made for  pH  and  specific
 conductance for each sample.  The instrument probes were not rinsed between
 replicate measurements; however, the probes were rinsed with deionized water
 prior to  replicate  measuring and upon completion of replicate  measuring.
 Specific  conductance and pH are temperature-sensitive measurements.* In
 several instances, the sample was allowed to rest several minutes between pH
 and conductivity measurements and was not retested for temperature prior to
 the  second set  of measurements.   Ambient temperature  should  be  a
 consideration for frequent temperature correction when making temperature-
 sensitive field measurements of this sort.

       Following field  measurements, filling sample  bottles commenced.
 USPCI 1986 quarterly sampling parameters appear in Table 13. Task Force
 personnel noticed the extremely rapid entry of water into the vials for volatile
 organics analysis (VOA).  The  resulting turbulence aerated the sample visibly.
 Aeration  strips the volatile organic compounds from the sample and should be
 avoided to the extent possible.  USPCI personnel later realized the error and
 reduced the rate of flow  into subsequent VOA bottles.

       USPCI sampling personnel wore latex surgical gloves to minimize the
 potential for sample contamination. These gloves were promptly changed upon
 contact with foreign surfaces; however, the Task Force observed that the
 samplers sometimes touched  the inside  surfaces of bottle caps with  their
 gloves, including the septa inside the caps of the  volatile organics bottles when
the septa jarred loose from the cap.  No effort was made to replace the caps or
 use a different bottle.  The samplers need to take care not to touch the insides of
the sampling containers with anything  other than the sample itself in order to
minimize contamination  from outside sources.
    Standard Methods for the Examination of Water and Wastewater. 15th edition, 1980.

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                                                                     73
                                Table 13
              USPCI QUARTERLY SAMPLING PARAMETERS*

         Parameter               Container             Preservative

      Volatile Organics       3 60-ml glass vials       Iced
      Appendix VIII, TOX     1-gallon amber  glass

      Total Organic          250-ml clear glass       H2SO4
      Carbon/Hardness

      Phenols               250-ml clear glass       H3PO4/CuSO4

      Metals                1-liter plastic             HNO3

      Total Dissolved        1 -liter plastic
      Solids/Alkalinity/
      Anions

      *   Parameters sampled when the Task Force observed UPSCI's quarterly
          sampling on July 9 and 10, 1986.  USPCI sampled these parameters
          because they were in assessment monitoring during 1986.  UDH and EPA
          Region VIII selected the parameters.

      A number of the monitoring wells were equipped at the  wellhead with
dedicated Teflon sampling tubing;  however, the  Task Force noted that in at least
two instances, a length of tubing was reused at consecutive wells without being
decontaminated between wells.   This  practice  introduces the possibility of
cross-contamination  between wells and should be discontinued.  Sampling
tubes should be either dedicated to the well or cleaned between wells.

      In the final quarter of 1985, USPCI began keeping a bound logbook of
each  sampling  event.  This  log contains information on weather conditions,
wellhead conditions,  field measurements and  any  extenuating circumstances
that might affect sampling. The sampling log should also document the types of
field instruments used and any changes in instrumentation.  Documentation of
early  1986 sampling was erratic.  USPCI needs to establish a  standard format

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                                                                    74
and completely document  all sampling.   Documentation of the July 1986
sampling was complete and  correct.

      Generally speaking, sampling practices at the USPCI facility are good,
with the exception of the deficiencies mentioned above. In the future, sampling
personnel need to pay close attention to the details of proper sample handling
and maintaining sample integrity.

Shipping and Chain-of-Custody

      Quarterly samples going to the USPCI-owned NAL laboratory in Tulsa,
Oklahoma were preserved as necessary, placed in ice chests on ice and sealed
for  shipping.    A  chain-of-custody  form and  analytical request sheet
accompanied each shipment.  Copies of these completed documents are kept
onsite.  Copies of the  chain-of-custody forms were provided to Task Force
personnel.  These forms contained spaces for the necessary information but
were not always completed  properly.  Several lacked notations for the  number
of sample bottles in the shipment for each parameter.  Sample bottle numbers,
specific to each bottle, were  not always recorded.

Sampling and Analysis Plan

      Task  Force  personnel observed  USPCI sampling  procedures for
adherence to the November 1985  sampling  and analysis plan.   USPCI
samplers used  the November 1985 sampling and analysis plan for the third
quarter sampling in July 1986.  Task Force personnel noticed that USPCI
personnel did not follow the plan on several points, thereby failing to comply
with UHWR 7.13.3 (40 CFR  265.92).

      The samplers did not  use a pH buffer in the 4.0 to 5.0 range of standard
in the field, as indicated by  the plan.  The samplers did not  return to pH 7.4
buffer after standardizing the meter at pH  10.4, as indicated  by  the plan, but
instead standardized at 7.4 first.

      The Company did not  follow the plan with respect to the preservative for
phenols.  The plan states that phenols will be preserved with  sulfuric acid

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                                                                   75
(H2SO4), but shipping forms and labels on sample bottles from the USPCI-NAL
laboratory specify the use of phosphoric acid and cupric sulfate (HPCVCuSCU).
When asked about this discrepancy, USPCI personnel indicated they will follow
laboratory instructions until the discrepancy is  resolved in  order to prevent
laboratory error  regarding  analysis of samples  and blanks.  This temporary
solution was acceptable, however, better communication with the laboratory
needs to be established so that the sampling and analysis plan reflects what is
actually done.  In other words, follow the plan.  Either  preservative is accept-
able; however, the preservative listed in the plan should either be changed to
HPO3/CuSO4, or H2SO4 (as indicated in the plan) should be the preservative
used for phenols.

      USPCI allowed a day's samples to wait overnight  and through  the
following day  before shipment; thus, they did not follow the schedule for
shipment in the plan.  The plan states that samples will be shipped immediately
after collection  and packing.

SAMPLE ANALYSIS AND DATA QUALITY EVALUATION

      The  sample  analysis and  data quality evaluation  for NAL are in
Appendix A.  The analyses and data evaluation for Task Force samples are in
Appendix B.

GROUND-WATER QUALITY ASSESSMENT PROGRAM

      The Grassy Mountain facility  entered a year of ground-water assessment
monitoring in the first quarter of 1986.  The following summary provides details
of events leading up to the  initiation of assessment monitoring and following its
implementation.

      On November 13, 1985,  USPCI notified the Utah Solid and Hazardous
Waste Committee that they  had measured statistically significant elevated levels
of total organic carbon (TOC) in MW-3.  USPCI also had measured elevated
TOC in upgradient and other downgradient wells on an  irregular basis, with no
apparent pattern. Quarterly sampling data  from December 9, 1985 showed
continued elevated TOC in MW-3.

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                                                                    76
      On December 12, 1985, UDH notified USPCI by letter that the ground-
water quality assessment plan was overdue and should have been submitted
within 15 days of the initial notification under UHWR 7.13.4 (40 CFR 265.93).
UDH formally requested that  USPCI submit the plan. USPCI  responded by
resubmitting their sampling and analysis plan on January 8, 1986.

      The sampling and analysis plan does not meet the basic requirements
for assessment monitoring under UHWR 7.13.4 (40 CFR 265.93).  The plan
does not:

            Specify clearly for which organic compounds  samples will be
            analyzed

            Specify the  appropriate  methods of  analysis for  organic
            compounds
            List and identify detection limits that NAL is  capable of achieving
            for the analyzable compounds
            Include  any  evaluation  procedures  for  the ground-water
            monitoring data, including analytical and water level data
            Make provisions for determining the rate and extent of migration of
            the  hazardous waste  or  hazardous waste constituents in the
            ground water

            Include complete and legible well construction specifications
      In effect, the USPCI Grassy Mountain facility had no ground-water quality
assessment plan,  as required by UHWR 7.13.4 (40 CFR 265.93).  Neither did
the facility have an outline of a ground-water quality assessment program, as
required by UHWR 7.13.4 (40 CFR 265.93).

      USPCI did, however, comply with instructions from UDH and EPA to
sample  and  analyze  for  selected* organic compounds quarterly  during
     Organic compounds to be analyzed for were selected by UDH and EPA Region VIII.

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                                                                   77
assessment  monitoring in  1986.  In this respect, USPCI was  following the
agency directives for assessment monitoring.

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                                                                   78

      GROUND-WATER MONITORING PROPOSED FOR FINAL PERMIT

      This section presents an evaluation  of the ground-water monitoring
program at Grassy Mountain as proposed for the final permit under UHWR 8.6
(40 CFR 264 Subpart F).  The section also includes proposed changes in the
ground-water monitoring system associated with expansion of hazardous waste
disposal activities at Grassy Mountain.

      USPCI received two  notices of deficiency for their Part B  permit
application from UDH.  With the second one, UDH  included a compliance
schedule  for the  permitting  process.   The compliance schedule included
submission of the hydrogeologic characterization report, which UDH received in
May 1986.   The three-volume report  includes  plans  for a ground-water
monitoring program proposed  for the final permit and was intended to be part of
the Part B application.  Because of the remote locations of MW-4, MW-6 and
MW-7, these wells may not provide useful monitoring coverage for those units
existing during  the Task  Force inspection.  The  Task Force evaluated  the
ground-water program proposed in this report with UHWR Part III criteria (40
CFR 270).

      The report outlines  a detection monitoring program pursuant to  UHWR
8.6.9 for the  uppermost aquifer and describes the proposed  monitoring well
network, monitoring parameters, sample analysis, sample collection and data
evaluation. The following discussion reflects the Task Force conclusions on
these items.

PROPOSED MONITORING WELL NETWORK

      As USPCI expands operations, the number of wells in the detection
monitoring program, under the permit, will increase above that in the  interim
status monitoring program.  UDH and EPA Region VIII propose that dedicating
wells to monitor each regulated unit is preferable to monitoring all the units as a
group.  This approach optimizes the chances  of detecting leakage from
individual  units.  Considering the low  hydraulic gradient,  the regulatory
agencies  also  propose the  placement  of  monitoring  wells so  that they
circumscribe the landfill cells (as opposed to downgradient only) in order to

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                                                                     79
 provide better detection coverage radially in the event a leak occurs through a
 cell liner.

      Wells MW-4, MW-6  and MW-7 are several hundred feet from  waste
 management  units and  cannot provide  immediate detection of leakage;
 however, they may provide useful water level data and periodic ground-water
 quality data.  USPCI is justified in proposing  to delete them from the required
 detection monitoring program under UHWR 8.6.9 (40 CFR 264.98) as long as
 expanded  operations do  not require these monitoring well locations  and
 hazardous  constituents have not been detected in wells located next  to the
 waste management units.

      For reasons stated in the section entitled "Well Construction," USPCI was
 unable  to demonstrate that monitoring wells MW-1  through  MW-8 were in
 compliance with UHWR 7.13.2 (40 CFR 265.91).  Special consideration of the
 construction of these wells needs to be given by the regulatory agencies prior to
 including these wells in a ground-water monitoring program under the permit.

      As for the land treatment areas, the existing, downgradient monitoring
 wells in the saturated zone combined  with the total of 16 lysimeters  in the
 unsaturated zone  should be adequate for compliance with 40 CFR 264.278 (in
 lieu of UHWR 8.13.19 which, when written, will be the State's corresponding
 regulation for unsaturated zone monitoring beneath  a land treatment area), and
 UHWR 8.6.8 and 8.6.9 (40 CFR 264.97 and 264.98).

      The  Task Force agrees with the identification of the  "shallow brine
 aquifer" as the uppermost aquifer, as defined by UHWR Part 1 (40 CFR 260.10).
 Wells completed in appropriate locations in this aquifer would  detect leakage
 earlier and more reliably than if they were completed in deeper, less permeable
 sediments.

      The  proposed design  for  future  monitoring well  construction is
acceptable. USPCI should,  however, provide to the State and EPA legible well
construction diagrams that completely show the design and position of each
well. The diagrams provided to the Task Force were not completely legible  and
complicated the verification of well specifications.

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                                                                     80

PROPOSED SAMPLING AND ANALYSIS PROGRAM

      Although the facility was in assessment during the inspection, leakage to
ground water from hazardous waste units has not been substantiated. Whether
or not the bottom liner has leaked hazardous constituents to the ground water
needs to be supported or refuted prior to selecting a ground-water monitoring
program for the final permit.

      Analysis of samples from the secondary leachate  detection system,
located between the two synthetic liners of landfill cell 2, indicates that the
upper liner has failed. USPCI  should be prepared to implement a compliance
monitoring  program  under UHWR 8.6.10 (40 CFR 264.99) in case the second,
lower liner of  cell 2 or liners of other units fail.

      The  list of proposed analytical parameters is too  comprehensive  and
includes some compounds that are not  analyzable by GC/MS.  USPCI should
develop a  list of parameters they can analyze."  Leachate analysis  would
provide guidance as to which chemical compounds or species USPCI should
monitor in  ground water.  Detection  limits that are attainable by the NAL
laboratory need to appear with each analytical parameter listed.

      The  analytical  procedures used to date by NAL have been judged  by the
Task Force to be incapable of accurately measuring hazardous constituents in
ground-water samples or of providing  a reliable indication of ground-water
quality [Appendix A].  NAL personnel should assess their laboratory capabilities
and protocols and propose analytical methods that they can do properly.

      The inconsistent sampling procedures that existed prior to the Task Force
inspection cannot ensure monitoring results that provide a reliable indication of
ground-water quality.  USPCI has taken  steps  to correct this problem  by
devising a sampling  and analysis plan (the deficiencies in this  plan have been
discussed in  the section  entitled "Ground-Water Monitoring Program During
    EPA requires a list [Appendix IX] of compounds that can be analyzed (Federal Register, Vol.
    52, No. 131, July 9, 1987, 25942).

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                                                                    81
Interim Status").  USPCI needs to ensure consistent sampling and analytical
procedures to comply with UHWR 8.6.8 (40 CFR 264.97).

      USPCI  has  proposed  to evaluate  ground-water  analytical data
statistically using the  Chemical Manufacturers' Association  (CMA)  standard
t-test.  This procedure is  inappropriate  for USPCI as it does  not take into
account other variables at Grassy Mountain, such as the naturally high salts in
the ground water  and the apparently  natural fluctuations  in  ground-water
quality.  USPCI should propose an evaluating method that accounts for this
variability.

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                                                                    82
    EVALUATION OF MONITORING DATA FOR INDICATIONS OF WASTE
                               RELEASE

      This section presents an analysis of the  Task Force monitoring data
regarding indications of apparent leakage from the waste management units.
Analytical results from and methods used on samples collected by Task Force
personnel are presented in Appendix B.  Ground-water samples collected by
the Task Force are identified in Table 14. Locations of leachate sumps sampled
are described in Table 15.

      Task Force data do not indicate the presence of organic compounds in
the 10 wells sampled.  The organic analyses  do not  detect  ground-water
contamination.  The analytical results for inorganics may reflect interferences
from the  naturally high salts in the ground water,  thereby making these results
unreliable.

      Collectively, both organic and inorganic chemical  analyses of leachate
provide evidence that the upper liner of landfill cell 2 has been breached in one
or more places and that hazardous waste constituents have migrated between
the two liners [Table 16].  In particular, leachate samples from sumps 3-B and
4-B show elevated concentrations of compounds one would  not expect to see if
the liner  were an effective partition separating hazardous  waste constituents
from the  leachate detection sumps.  Followup sampling and analysis  may be
desirable to confirm or refute this conclusion.

      The organic constituent analysis results of samples from the leachate
detection system in cell 2 indicate the presence  of elevated levels  of several
organic compounds.  Methylene chloride was detected at 1200  fig/L in sump
3-B and 245 ng/L in 2-B, whereas concentrations in 1-B and 4-B were much
lower at 36 and 31 p.g/L, respectively.  The compounds 2-butanone (970 |j.g/L)
and acetone (270 ng/L) were detected in sump 4-B, but were not detected in the
other sumps of cell 2.

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                                                             83
                           Table 14
                 MONITORING WELLS SAMPLED BY
                         TASK FORCE
               Well
                MW-3
                MW-7
                MW-9
                MW-10
                MW-11
                MW-13
                MW-14
                MW-15
                MW-16
                MQ-17
                     Sample Number
                        MQ0545
                        MQ0539
                        MQ0548
                        M00537
                        MQ0536
                        MQ0541
                        MQ0540
                        MQ0543
                        MQ0549
                        MQ0550
                           Table 15
           LEACHATE SAMPLE LOCATION DESCRIPTIONS
Unit
Sump Designation
   Location
Sample Number
Cell 1
Cell
Cell
Cell
Cell
    Cell 1

    1-B
    2-B
    3-B
    4-B
Surface
Impoundment
Southern end of
 CelM
Northeast corner
Southeast corner
Southwest corner
Northwest corner
West end
    MQ0396

    MQ0394
    MQ0395
    MQ0393
    MQ0392
    MQ0538

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                                                                   84
                               Table 16
   SELECTED COMPOUNDS FOUND IN LEACHATE SAMPLES FROM THE
              LEACHATE DETECTION SYSTEM OF CELL 2*

                    	    	    Sumps	
                   Units*
1-B
2-B
3-B
4-B
                      Organic Constituent Analysis
Methylene
Chloride
2-Butanone
Tetrahydrofuran
Phenol
2-Methylphenol

H9/L
^g/L
jig/L
W/L
W/L

36
ND
850
ND
ND

245
ND
1100
ND
ND

1200
ND
240
1500
980

31
270
7800
ND
ND
                           General Analysis
Purgeable Organic
Halogens (POX)
Nonpurgeable
Organic Carbon
(POC)

Chromium, Cr
Iron, Fe
Potassium, K

mg/L Cl


mg/LC

W/L
M/L
W/L

27


43
Metals Analysis
34
67
259,000 221

34


57

34
37
,000

840


223

20,000
280
1,560,000

160


91

684
13,200
240,000
    Complete analytical results appear in Appendix B.
        , micrograms per liter; mg/L, milligrams per liter; C, Carbon; Cl, Chloride.
      Tetrahydrofuran was detected in each of the sumps of cell 2, ranging
from 240 |ig/L in sump 3-B to 7800  p.g/L in sump 4-B.  The presence of
tetrahydrofuran in Task Force samples was confirmed by an independent NEIC
laboratory analysis.
      Phenol and 2-methylphenol were detected in sump 3-B at 1500 ng/L and
980 ng/L, respectively, but were not detected in sumps 1-B, 2-B and 4-B.

      Leachate analyses  for 3-B also indicate elevated purgeable organic
halogens (POX) at 840 |ig/L Cl and 160 ng/L in 4-B.  The presence of POX
beneath the upper liner is significant because most halogenated organics rarely

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                                                                     85
occur in nature.* Consequently, the Task Force concludes that the occurrence
of purgeable organic halogens at such levels in the leachate detection system
suggests that the upper liner in cell 2 has leaked.

      The level  of  nonpurgeable  organic carbon  (NPOC) in sump  3-B
(223 mg/L) exceeds those levels in 1-B (43 mg/L) and 2-B (57  mg/L) by about
four times and is two times  higher than the NPOC in 4-B (91  mg/L).   The
analytical results for NPOC show a similar  pattern to that exhibited by POX,
supporting the conclusion that the upper synthetic liner has been breached,
probably somewhere in the western half of cell 2.

      Task Force  data indicated  elevated chromium  levels  in  leachate
detection sump 3-B in the southwestern quadrant of cell 2 (20,000 |ig/L) and in
sump 4-B  in  the  northwestern quadrant of cell 2 (684 |ig/L).  By contrast,
analyses of  leachate  samples from  the  northeastern and southeastern
quadrants (1-B  and  2-B,   respectively)  each  indicate  chromium  in  a
concentration of 34 p.g/L  The leachate analysis  for unlined cell 1  indicates
chromium at 134 |ig/L

      Iron in  leachate sump 4-B was measured at 13,200 jj.g/L, 47 times the
concentration  of iron (Fe) in 3-B (280 |ig/L) and more than  150 times the
concentration of iron in 1-B and 2-B.  The cause of elevated iron  in 4-B is
unknown.

      The leachate sample from sump 3-B  had a  potassium concentration of
1,560,000 ^ig/L, which is seven times greater than in other sumps of cell 2.
Although potassium is not listed in 40 CFR 261 as a toxic metal, the higher
levels in 3-B suggest the leachate in that sump has been affected by potassium-
bearing waste streams in the landfill cell.

      Samples fFOflv^raund-water_monitoring wells near  cell  2 do not show
chemical evidence that the bottom liner has leaked.
     Takahashi, Y; Moore, R.T.; and Joyce, R.J., "Measurement of Total Organic Halides (TOX)
     and Purgeable Organic Halogens (POX) in Water Using Carbon Absorption and
     Microcoulometric Determination," Chemistry in Water Reuse, Volume 2, 1981

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                           REFERENCES
1.    EPA RCRA Ground-Water Monitoring Technical Enforcement Guidance
      Document (TEGD), OSWER 9950.1, September 1986

2.    McGraw, Jack, EPA  Memorandum on  "Procedures for Planning and
      Implementing Offsite Response", May 6,1985.

3.    USPCI Transmittal to  U.S. EPA Region VIII, Exhibit C, "Impoundment A
      Capacities", September 28,  1984.

4.    USPCI, 1985 "Grassy Mountain Facility, EPA Biennial Report" (RCRA
      Annual Report).

5.    USPCI "Waste Analysis Plan", August 22, 1985 (PRC. Vol. 9, T017-P09-
      601-010, Attachment B).

6.    USPCI, "Response to Federal Ground-Water  Regulations 40  CFR
      170.14(c) Regarding  Grassy  Mountain Facility Near  Knolls, Utah",
      Volumes 1, 2 and 3, May 1986.

7.    Freeze, R. A., and Cherry, J. A. 1979. Groundwater. Prentice-Hall Inc.,
      Englewood Cliffs, New Jersey, 604 p.

8.    Driscoll, F. G., ed  1986. Groundwater and Wells. Johnson Division, St.
      Paul, Minnesota, 1089 p.

9.    Federal Register. Vol. 52, No. 131, July 9, 1987, 25942.

10.    Takahashi, Y., Moore, R. T. and Joyce, R. J., "Measurement of Total
      Organic Halides (TOX) and Purgeable Organic Halides (POX) in Water
      Using  Carbon  Absorption  and Microcoulometric  Determination,"
      Chemistry in Water Reuse, Vol. 2,1981.

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                  APPENDICES

A    USPCI SAMPLE ANALYSIS AND DATA QUALITY EVALUATION
B    ANALYSIS AND DATA EVALUATION FOR TASK FORCE
     SAMPLES

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                  APPENDIX A



USPCI SAMPLE ANALYSIS AND DATA QUALITY EVALUATION

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                                                                   A-1

                              Appendix A

       USPCI SAMPLE ANALYSIS AND DATA QUALITY EVALUATION

      This section provides an evaluation of the quality and completeness of
ground-water monitoring data gathered by USPCI between March 1982  and
June  1986.  Mideco  Laboratories  performed analyses for the first quarter of
1982 and Ford Laboratories provided analyses for the second quarter.  National
Analytical  Laboratories (NAL) has been responsible for the analytical work for
USPCI since August 1982.  USPCI personnel  at the  site performed some
measurements for specific conductance and pH.   NAL was  evaluated
concurrently  with the onsite inspection  of the  USPCI facility.  During the
laboratory  evaluation,  operating  and analytical procedures, internal data
reports, raw data and quality control records  were reviewed and analytical
equipment was examined.

      The inspection revealed analytical inadequacies and found that much of
the monitoring required in 1982 and 1986 has not been performed.  Most
analytical  inadequacies  stem from improper sample handling or calibration
procedures, the lack of quality control measures,  and/or not accounting for the
high dissolved solids content  of the sample.   The  initial  year of  required
background quarterly  monitoring conducted in 1982 was incomplete as was the
monitoring  conducted in 1986.  These inadequacies adversely affected the
reliability of data in establishing background levels or in detecting releases  into
the ground water. A detailed discussion of these inadequacies is given in the
following sections.

Ground-Water Analysis. 1982 through 1985

      UHWR 7.13.3 (40 CFR 265.92) requires quarterly monitoring of all wells
during the initial year to establish background values.  Quarterly monitoring of
the upgradient wells  must include quadruplicate measurements of  the four
parameters used  as  indicators of ground-water contamination (pH, specific
conductance, TOG and TOX).   In  March 1982 USPCI initiated  quarterly
monitoring pursuant to  7.13.3.(c) on the RCRA well network.  The  network
included upgradient wells 1 and 2 and downgradient wells 3 through 8. UDH

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A-2

required  USPCI to restart background monitoring at the  beginning of 1983,
because of the incompleteness  and the poor  data quality of the 1982
monitoring.

      The  first year of background water quality  monitoring in 1982 was
incomplete.  The required quadruplicate measurements for the four indicator
parameters for upgradient wells were not reported.  Background monitoring
results for the required pesticides, herbicides and the  radiochemical parameters
were not reported at  all (UHWR 7.13.3  and 40 CFR Part 265.92). Fluoride,
nitrate  and pH  were not reported for the fourth quarter.  TOG and coliform were
not reported for the first and second quarters and TOX was not reported for the
third and fourth quarters.  Silver was not reported in the fourth quarter of 1982
and chromium was not reported for the first quarter of  1983.   Subsequent
monitoring  through  1985 monitoring was complete; all monitoring suffered
analytical deficiencies.

      Holding times  for  pH  measurements were  exceeded.   Between
November  1983 and August  1984, pH was  measured  after samples were
shipped to NAL in Oklahoma rather than analyzed on site. Prior to 1984, the
EPA-recommended holding time was 2  hours.   Since  1984, EPA has
recommended that samples be analyzed immediately.  Due to  the susceptibility
of pH  to change with  time for ground water samples,  the pH  results for
November 1983 to August 1984 are unreliable.

      Specific  conductance results  are suspect. Cell constant  corrections have
not been made for the measurements. Further, standards  to establish the cell
constant were  not within the same range as the samples.  The lack of these
measures causes bias in the results.  A detailed explanation of cell corrections
can be found in Standard  Methods. 15th edition, and in the instruction manual
for the particular instrument.

      The standard TOX method can often achieve a detection limit of between
5 |ig/L  and 30 |ig/L; however, the high chloride levels in the site ground-water
samples  would prevent such  a detection limit  from being achieved.  High
chloride levels can cause TOX results to be biased high.  Typically 50 mg/L
chloride could cause an apparent TOX of 1  mg/L.  Some of the ground-water

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                                                                   A-3
samples have been found to contain as much as 50,000 mg/L chloride.  Such
samples could cause an apparent TOX of 1,000 jig/L.

      Some  of the samples also have a  high turbidity which infers  high
suspended solids.  In 1982, at least some of the samples were filtered prior to
analyzing for TOX.  Between 1982 and the beginning of 1986, records do not
clearly indicate if samples were filtered or not. Filtering could cause TOX values
to be biased low  due to  the loss of volatile organics and  the sorption of
dissolved organics.  However,  TOX could be biased  high if the paniculate
matter contained  chloride  and it is not removed.  Further, the high sodium
content  of these samples can cause the quartz furnace of the TOX analyzer to
deteriorate resulting in  a negative bias for TOX measurements.

      TOX measurements using the standard method and instrumentation for
ground  water containing such high levels of dissolved salts  and suspended
solids can not serve as an indicator of low level contamination of halogenated
organics and thus the reported  TOX results are unreliable.  POX (purgeable
organic halogens) measurements could serve as an  indicator of low level
contamination of volatile halogenated organics, assuming proper care is taken
to ensure the quartz furnace does not deteriorate due to an excessive purge
rate introducing  sodium into the furnace.

      TOC was determined by acidifying and purging samples prior to analysis.
The results for this type of measurement are best termed nonpurgeable organic
carbon  (NPOC) as the purging not only eliminates inorganic carbon from the
measurement but also purgeable organic carbon (POC).  To indicate that NPOC
results are equivalent to TOC results would require the measurement  of POC to
establish that POC does not contribute significantly to the TOC.

      Mercury  has been exclusively determined  by cold vapor atomic
absorption spectroscopy.  Prior to 1983, NAL used sodium borohydride as the
reductant. The  EPA method uses stannous chloride. NAL personnel indicated
that they started using stannous  chloride as the reductant for the mercury
determinations sometime in 1983.

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A-4
      Mercury was detected in only two quarters. In the last quarter of 1982, all
well samples were reported to contain mercury at concentrations in excess of
the drinking water standard of 2  (ig/L  The reported values ranged from 3 |j.g/L
to 6 |ig/L  In the  next sampling in March of  1983,  five well samples were
reported to contain mercury at concentrations ranging from 0.4 |ig/L to 2.5 |ig/L.
Previous and subsequent to these two instances,  mercury was not detected.
The positive  results observed for these two samplings  are  probably  due to
systematic error caused by the laboratory and probably do not represent actual
concentrations in the well samples. The error  may have been caused by the
use of the sodium borohydride  reductant or could possibly be introduced, as
NAL did not take steps  to eliminate interference  due to  the formation of chlorine
from chloride during the oxidative digestion in the procedure.

      Many of the  determinations for the other metals or elements are
unreliable  because the  high dissolved solids content  of the ground-water
samples have caused  serious interference.  Atomic absorption spectroscopy
techniques were exclusively used for metals determinations, except  barium,
until 1985. The high salt concentration causes so much molecular background
that the analyte atomic  absorption signal cannot be distinguished reliably by the
furnace background correction instrumentation.  Further, ionization interference
would have been severe for the flame technique.

      In 1983, NAL started to  use Zeeman background correction furnace
atomic absorption spectroscopy for some of the metals determinations. The
Zeeman technique can compensate for larger molecular interference than the
continuum background correction system  used previously.  However, the
implementation of the Zeeman technique did not resolve all the sample matrix
effects and much of the  data are  unreliable.

      In 1985, NAL started to use Inductively Coupled Argon Plasma Optical
Emission Spectroscopy (ICP) instead-of-Atomic^Absorption Spectroscopy for
some of the other metals determinations.  ICP is also  subject to interferences
due to high dissolved solids.  The ICP background generally increases with
increasing  dissolved solids content and signal to concentration  calibration
changes with increasing dissolved solids which is partially due to changes in
the sample introduction  rate and  changes in the  plasma emission profiles of the

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                                                                    A-5

analytes.  Apparently cognizant of the problems with high  dissolved solids in
ICP analyses, NAL analyzed dilutions of samples.  Diluting the sample will help
to eliminate interference but dilution compromises the detection limit. Typically,
ICP can often achieve detection limits of 2 jig/L for cadmium and 30 fig/L for
lead.  At the  1:10 dilution used by NAL, the detection limits for cadmium and
lead would at least  have been 20 ^.g/L and 300 (ig/L, respectively.  Both
detection  limits exceed the respective drinking water standards for cadmium
and lead  and are not low enough to reliably  establish background levels for
ground water.

      The ground-water sample  matrices challenge many of the commonly
used  methods for metals determinations.  Reliable  results that established
background levels have not been obtained using these methods.  Methodology
common to low level determinations in seawater could possibly provide such
results.  Extraction and coprecipitation isolation techniques are  used prior to
atomic absorption or ICP spectroscopic analysis.  Direct analysis without the
use of isolation techniques may prove successful.  The method of standard
additions in an ICP analysis for barium, cadmium, chromium, iron, sodium and
silver would  be a possibility.  Alternately, exact matching of the calibration
standards to  the ground-water  sample matrix  for ICP  analyses  may be
appropriate.  ICP analysis of  dilutions for barium, iron and sodium may be
successful. Cadmium, chromium, lead and silver could probably be determined
by furnace atomic absorption spectroscopy. The use of Zeeman background
correction, the L'vov platform, matrix modifiers possibly including palladium and
absorbic  acid, as well as appropriate dilutions should facilitate the furnace
technique analyses.  Arsenic and selenium could be  determined  by  hydride
generation atomic spectroscopy. Mercury should continue to be determined by
cold vapor atomic absorption spectroscopy although purging  of the digests prior
to the addition of the reductant should be employed to circumvent possible
interference due to the formation of chlorine. The use of any technique must be
predicated on achieving detection limits well below the drinking water
standards  established in UHWR, Appendix E (40 CFR 265, Appendix III).

      A number of laboratory records for metals and  pesticides determinations
that were  performed  for ground-water samples prior to and around mid-1985
could  not be located by NAL personnel. A large turnover in both analysts and

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A-6
managers at NAL has resulted in some discontinuity in the way samples have
been processed at the lab  since early 1983.  The  lack of records for the
pesticide determinations prevented  evaluation of the data  quality  for these
parameters.

      Data reported for the phenoxy acid herbicides, 2,4-D and Silvex, are not
reliable. The method used would not detect the herbicides present in the ester
form.  A reliable method, such as the one  recommended  under the Safe
Drinking Water Act, would detect the herbicides present in both the acid and
ester forms.   Problems with the method are illustrated  when  NAL  failed to
achieve acceptable  results  for 2,4-D in  a State of Kansas performance
evaluation for drinking water certification in 1984.

      Gross alpha and gross  beta  activity  measurements have  been made
subsequent to  1982.   Many of the  gross alpha values  are  reported as not
detected at the maximum contaminant level  of  2 pCi/L (40 CFR Part 265,
Appendix III).   This detection  limit is achievable for samples containing low
levels of dissolved solids, but not for samples containing percent levels of
dissolved solids.  Analytical methods require the use of smaller aliquots of
samples containing  high  levels of  dissolved  solids resulting in increased
detection limits.  For  samples containing  50,000 mg/L dissolved  solids  a
detection limit  of about  100 pCi/L gross alpha and 200 pCi/L  gross beta would
normally be achieved.  Thus  the gross alpha and gross beta data as reported
are not reliable.

      NAL personnel indicated that  some of the resulting distillates from the
phenol determinations were noticeably turbid.   The colorimetric analysis of  a
turbid distillate  could cause a high bias and may account for the anomalous
detection of phenol in  some of the  samples.   NAL was  planning to use the
chloroform extraction  procedure  which should circumvent the  turbidity
interference for future determinations.

Ground-water Analysis Commencing  January 1986

      USPCI restarted  background ground-water quality monitoring at the
beginning of 1986.  The new sampling and analysis plan called for monitoring

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                                                                   A-7
wells 1 through 7 and wells 9 through 20.  Parameters were added to those
included in previous sections of this report.  No results could be found for well 5
during the first quarter  of  1986.   According  to  UDH,  only volatile  and
semivolatile organic compounds were reported for the second quarter of 1986
for all the wells.  All other analyses required by the sampling and analysis  plan
were not reported (e.g., metals were not reported for the second quarter).

      Most of the laboratory findings discussed in the previous section are  also
applicable  to  the  1986  data, as  most of the  methods  did  not  change.
Determinations still lacked adequate quality control measures. NAL used gas
chromatography/mass  spectrometry (GC/MS)  methods for the pesticides
determinations rather than the gas chromatography methods used previously.
The GC/MS methodology  cannot achieve detection limits below drinking water
standards and thus can not reliably establish  background  levels.  NAL  was
using a more  appropriate method (including  the ester form)  for herbicide
determinations  at the time  of the Task Force inspection.

      The volatile and semivolatile organic  results for the first two quarters of
1986  should be considered unreliable.  Methods 624 and 625* were cited as
being used, however, the  cited methods were not properly followed. Accuracy
and  precision  control measures required by the methods  were  not properly
implemented or evaluated.  For example, the mass spectrometer was  not
properly calibrated  for the Method 624 analyses.  Bromofluorobenzene (BFB)
was  not used  to check the instrument  calibration, as required.  In  addition,
purgeable gases could not be  detected at concentrations at least 20 times the
normal method detection  limit of 5  jig/L.   Reported GC/MS detection limits
should be considered an estimate as  they were taken from  the published
method without having performed the actual determination required by the
methods.

      Reportedly, during  1986, TOX samples were  not filtered  as is proper.
Other comments relative to TOX, as presented in the section above, continue to
apply.
    40 CFR Part 136

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                   APPENDIX B



ANALYSIS AND DATA EVALUATION FOR TASK FORCE SAMPLES

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                                                                            B-l

 II.   Evaluation of Quality Control Data and Analytical Data

 1.0   Metala

 1.1   Performance Evaluation Standards

      Metal analyte performance evaluation standards were not evaluated in
 conjunction with the samples collected from this facility.

 1.2   Metals QC Evaluation

      Total metal spike recoveries were calculated for twenty-three metals spiked
 into two ground-water samples (MQO539 and 546) and two leachate samples
 (MQO392 [graphite furnace metals only] and MQO393 [ICP metals and mercury
 only]).  Six average spike recoveries from the ground-water samples and eight
 individual spike recoveries from the leachate samples were within  the data quality
 objectives (DQOs) for this Program.  Spike recoveries for four of the metals  from
 the ground-water samples and seven of the metals from the leachate samples  were
 not calculated because the sample concentrations were greater than four times the
 concentration of spike added. In the ground-water samples, the cadmium, lead, and
 selenium average spike recoveries were above DQO with values of  560, 3250, and 440
 percent, respectively. The barium, beryllium, chromium, cobalt, copper, manganese,
 nickel, silver, thallium, and zinc average spike recoveries were below DQO with
 values of  18, 69, 70, 67, 45, 37, 66, 0, 26, and 69 percent, respectively.  Various
 individual metal spike recoveries from the  ground-water samples were also outside
 DQO.  These are listed in Table 3-2a of Reference 2  as well as in the following
 Sections.  In  the leachate samples, arsenic, cadmium,  lead,  and manganese spike
 recoveries were above DQO with values of  240, 226, 444, and  188 percent,
 respectively.  The  barium, mercury, silver, and thallium spike recoveries were below
 DQO with values of 25, 16, 26, and 57 percent, respectively. Only  one leachate
 sample was spiked for each metal. Sample MQO392 was spiked for the furnace
 metals and sample MQO393 was spiked for  the ICP metals.

      All reported  laboratory  control sample (LCS) recoveries and all calibration
 verification standard (CVS) recoveries were within Program DQOs.

     The average  relative percent differences (RPDs) for all metallic analytes in
 both ground  water and leachate, except selenium in a leachate sample, were within
 the DQOs.

     Required analyses were  performed on all metals samples submitted to the
 laboratory.

     No contamination was reported in the laboratory or sampling blanks.

 1.3   Furnace Metals

     The furnace metals  (antimony, arsenic, cadmium, lead, selenium,  and thallium)
quality control, with a few exceptions, was acceptable. The traffic reports for
samples MQO549 and 550  were not included in the data package from  the laboratory.

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  B-2
     All antimony results, with the exceptions of samples MQO394, 395, 545, 546,
and 550, should be considered quantitative.  Duplicate injection precision for
antimony was outside DQO for samples MQO394, 395, 545, 546, and 550.  Because of
this, antimony results for samples MQO394 and 550 should be considered qualitative
while those for samples MQO395, 545, and 546 should be considered unreliable.

     The arsenic spike recoveries for samples MQO392 (leachate sample), 539
(ground-water sample), and 546 (ground-water sample) were outside DQO with
recoveries of 240, 155, and 0  percent, respectively. The correlation coefficients for
the method of standard addition analysis of  two arsenic laboratory control standards
(LCS*1 and LCS*2) were outside of DQO. Duplicate injection precision was outside
DQO for arsenic in samples MQO547, 548, and 549.  Arsenic results, with the
exceptions listed below, should be considered unreliable due to the above problems.
Arsenic results for samples MQO542, 544, and  551 should  be considered semi-
quantitative and results for samples MQO392 and 396 should be considered
qualitative.

     The cadmium spike recoveries for samples MQO392 (leachate sample), 539
(ground water), and 546 (ground water) were outside  DQO with recoveries of 226,
50,  and 1070 percent,  respectively. Duplicate injection precision was outside DQO
for cadmium in samples MQO546 and 547. Cadmium results, with the  exceptions
listed  below, should be considered qualitative. Cadmium results for samples
MQO542, 544, and  551 should be considered  semi-quantitative and results for samples
MQO546 and 547 should be considered  unreliable.

     The  lead spike recoveries for samples MQO392 (leachate sample)  and 546
(ground-water sample) were outside DQO with recoveries  of 444 and 3250 percent,
respectively.  The correlation coefficients  for the method  of standard  addition
analysis of three lead samples (MQO393 and  395) were outside of DQO.  Lead
results, with the exceptions listed below, should be considered unreliable due to the
above problems.  Lead results for samples MQO542, 544, and 551 should be
considered semi-quantitative.

     The selenium spike recoveries  for samples MQO392 (leachate sample) and 539
(ground-water sample) were outside DQO with recoveries  of 0 and 440 percent,
respectively.  Duplicate injection precision was outside DQO for selenium in samples
MQO541,  545, 546Dup, 549, and 550. A duplicate injection  was not run for sample
MQO539.  Selenium results, with the exceptions mentioned below, should be
considered unreliable  due to the above  problems.  Selenium  results for samples
MQO542,  544, and  551 should be considered  semi-quantitative and results for
MQO393,  394, 396, 536, 537,  540, and 543 should be considered qualitative.

     The  thallium  spike recoveries for  samples MQO392 (leachate sample), 539
(ground-water sample), and 546 (ground-water sample) were outside DQO with
recoveries of 57, 51, and 398 percent, respectively.  Duplicate injection precision
was outside DQO for  thallium in sample MQO543. All thallium results should be
considered qualitative.

-------
                                                                            B-3

     All aluminum, calcium, magnesium, sodium, and vanadium results should be
considered quantitative.  All beryllium, chromium, cobalt, iron, nickel, and potassium
results, as well as zinc results with the exceptions listed below, should be
considered semi-quantitative.  All barium, copper, and manganese results, as well as
zinc results for samples MQO392, 393,  394, 395, and 396, should be considered
qualitative. All silver results should be considered unreliable.

1.5  Mercury

     Some samples which were analyzed for mercury required additional dilution.
Mercury detection limits for these samples were raised and false negatives are a
possibility.

     The mercury spike recovery for the leachate spike (MQO393) was biased low by
84 percent (16 percent recovery). All non-detect mercury results for leachate
samples are unreliable (high probability of false negatives). All positive mercury
results in the leachate samples are qualitative.

     All mercury results, with the exceptions of results for the leachate samples
(MQO392, 393, 394, 395, and 396), should be considered quantitative with an
acceptable probability of false negatives.  Mercury results for leachate samples
MQO393, 394, and 396 should be considered qualitative and results  for MQO392 and
395 unreliable.
2.0  Inorganic and Indicator Analvtes

2.1  Performance Evaluation Standard

     Inorganic and indicator analyte performance evaluation standards were not
evaluated in conjunction with the samples collected from this facility.

2.2  Inorganic and Indicator Analvte OC Evaluation

     The average spike recoveries of all of the inorganic and indicator analytes, in
both ground water and leachate, were within the accuracy DQOs (accuracy DQOs
have not been established for bromide and nitrite nitrogen matrix  spikes).  This
indicates acceptable recoveries for all inorganic and indicator analytes.

     All LCS and CVS recoveries reported in the raw data for inorganic and
indicator analytes  were within Program DQOs.

     Average RPDs for all inorganic and  indicator analytes were within Program
DQOs.  Precision DQOs have not  been established for bromide and nitrite nitrogen.

     Requested analyses were performed on all samples for the inorganic and
indicator analytes.

     No laboratory blank contamination  was reported for any inorganic or indicator
analyte.  Contamination involving POX, total phenols, and TDS was found  in the
sampling blanks (MQO542, 544, and 551) at levels above CRDL. ^T-hese_CQfliaminants
and their concentrations are listed below, as well as in Section 3.2.4 (page 3-2) of
Reference 2. ^

-------
B-4

 2.3   Inorganic and Indicator Amlvte Data

      The quality control results for cyanide, sulfate, sulfide, chloride, and total
 dissolved solids (TDS) are acceptable. The results for these analytes should be
 considered quantitative.

      The holding times  for the nitrate nitrogen analyses ranged from six to eight
 days from receipt of samples which is longer than the recommended 48 hour  holding
 time for unpreserved samples. The nitrate nitrogen results should be considered
 semi-quantitative with detection limits raised by a factor of 1000 due to dilutions
 required by the high concentrations of sulfate and chloride present in  the samples.

      The holding times  for the nitrite nitrogen analyses ranged from six to eight
 days from receipt of samples which is longer than the recommended 48 hour holding
 time for unpreserved samples. The laboratory did not analyze an initial calibration
 verification (ICV) at the beginning of the nitrite nitrogen ion chromatography
 analytical batch,  as requirrd.  The nitrite nitrogen results should be considered to
 be semi-quantitative with detection limits raised by a factor of 1000 due to dilutions
 required by the high concentrations of sulfate and chloride present in  the samples.

      The laboratory did not analyze an ICV at the beginning of the bromide ion
 chromatography analytical batch, as  required. The bromide results should be
 considered to be semi-quantitative with detection limits raised  by a factor of 1000
 due to dilutions required by the high concentrations  of  sulfate  and chloride present
 in the samples.

      One of three ammonia nitrogen matrix spikes (into a ground-water sample) was
 above the  DQO with a recovery of 114 percent (DQO range 90  to 110 percent).  All
 ammonia nitrogen results should be considered semi-quantitative.

      One of three total  phenols  matrix spike recoveries  (into a  leachate sample) was
 above the  DQO with a recovery of 122 percent (DQO range 80  to 120 percent).
 Total phenol contamination was found in the trip and field  blanks (MQOS42, 544,
 and SSI) at concentrations of 52, 20, and 520 ug/L.  These values are above the
 total phenol CRDL of 10 ug/L.  All total phenols results greater than 10 times the
 highest concentration of total phenols in the field blanks or less than the detection
 limit are considered semi-quantitative.  This includes samples MQO392, 393, 394, 395,
 396, 540, 543, and 548.  All other total phenols results arc unreliable.  Many of the
 total phenols samples were diluted by 2 to 20 times normal dilutions.  This results
 in raised detection limits for the affected samples.

      A final TOC calibration verification (CV) and final calibration blank  (CB) were
 not analyzed for one of  the analytical batches.  Results  for sample MQO393 and the
 spike analysis  results for MQO396 were affected. The agreement of results between
 one of the field triplicates and the other two was poor with  reported TOC
 concentrations of 1000 (an estimated concentration because 1000 ug/L  is the  .
 detection limit), 8100, and 8500 ug/L. The comparative  precision of the field
 triplicate results is not used in the evaluation of sample data as it  is not possible
 to determine the source  of this imprecision. Field triplicate precision is reported
 for informational purposes only. The 28 day TOC holding time was exceeded by one
 to three days.  All TOC  results should be considered semi-quantitative.

-------
                                                                           B-5
     Initial calibration verification and continuing calibration verification (CCV)
standards for POC were not analyzed.  EPA needs to supply the inorganic laboratory
with a POC calibration verification solution.  Until then,  the instrument calibration
can not be assessed.  The POC results should be considered qualitative.

     A CCV and CCB were not run at the end of each days TOX analytical batches.
Instrument calibration curve information for TOX was not provided in the raw data.
High levels of chloride (above 200 mg/L) were found in all field samples. All
samples had to  be diluted by as much as 100,000 to 1 because of this interference.
Most of the TOX results, except for the blanks, are unreliable with greatly
increased detection limits.  The TOX results for the sampling blanks should be
considered quantitative.

     Field blank MQOS51 contained POX contamination at 20  ug/L which is above
the CRDL.  All POX  results greater than 10 times the highest concentration of  POX
in the  field blanks (samples MQO393 and 539) should be considered quantitative and
all POX  results greater than 4 times the blank concentration (samples MQO392)
should be considered qualitative.  The other POX results should be considered
unreliable.

     The field  triplicate RSD was 41 percent for TDS  which the data reviewers
consider  excessive. The comparative precision of the field triplicate results is not
used in the evaluation of sample data as it is not possible  to determine the source
of this imprecision.  Field triplicate precision  is reported for informational  purposes
only.  No laboratory  blanks were analyzed for TDS. One field  blank had TDS
contamination of 4000 ug/L. This contamination level was so much lower than field
sample results that it was felt to have no impact on the field sample results.  As
mentioned previously, the TDS data should be considered quantitative.

3.0   Organics and Pesticides

3.1   Performance Evaluation Standard

     Organic performance  evaluation standards were not evaluated in conjunction
with the  samples collected from this  facility.

3.2   Organic OC Evaluation

     All  matrix spike average recoveries were within established Program DQOs  for
accuracy.  Individual matrix spike recoveries which were outside the accuracy  DQO
will be discussed in the appropriate Section below. All surrogate spike average
recoveries were also  within DQOs for accuracy.  Individual surrogate spike
recoveries which  were outside the accuracy DQO will be discussed in the
appropriate Section below.

     All  matrix spike/matrix spike duplicate average RPDs were within Program
DQOs for precision except those for phenol and 2-chlorophenol. Individual matrix
spike RPDs which were outside the precision DQO will be discussed in the
appropriate Section below.  All average surrogate spike RPDs were also within  DQOs
for precision except those for phenol-D5, 2-fIuorophcnol, and dibutylchlorendate.

     All  organic analyses were performed  as requested.

-------
B-6

     Laboratory blank contamination was reported for organics and is discussed  in
the appropriate Sections  below.

     Detection limits for the organic fractions are summarized in the appropriate
Sections below.

3.3  Volatiles

     Quality control data indicate that volatile organics  were determined acceptably.
The chromatograms appear acceptable.  Initial and continuing calibrations, tunings
and mass calibrations, blanks, matrix spikes, matrix spike duplicates, surrogate
spikes, and holding times are all within acceptance limits.

     Acetone was found in five laboratory blanks at values of 5 to 12 ug/L.  The
CRDL for acetone is  10 ug/L.  Acetone results in this range should be considered
unreliable.

     Estimated method detection limits are CRDL for all samples except QO392
which is 10 times CRDL, QO393 which is 7.7 times CRDL, and QO396 which is :.
times CRDL.

     The volatiles data are acceptable.  The probability of false negative results  for
the volatiles is acceptable except for the three samples with raised detection  limits.
The volatile compound results should be considered quantitative.

3.4  Semivolatiles

     Calibrations,  tuning and  mass calibrations, blanks, matrix spikes, matrix spike
duplicates, surrogate spikes, holding times, and chromatograms were acceptable for
the semivolatiles.

     The matrix spike (but not matrix spike duplicate) recovery of 2-chlorophcr.  .
was 25 percent  which is below the DQO of 27 to 123 percent. The matrix spike
and matrix spike duplicate RPDs for phenol (72 percent) and 2-chlorophenol (77
percent) were above the DQO limits of 42 and 40 percent, respectively.

     The surrogate percent recoveries for phenol-D5 in samples QO543RE
(reextraction  or reanalysis), 549, and 549RE, 2-fluorophenol in samples QO543,
543RE, 549,  549RE, and 550, and 2,4,6-tribromophenol  in sample QO396  were below
their DQOs.  These low recoveries  will adversely affect the usability of the acid
fraction results.

     The semivolatile data are acceptable and the results should be considered
quantitative except for the acid fraction results for samples QO396, 543, 549, and
550 which should be considered  unreliable due to poor surrogate recoveries.
Estimated method detection  limits are CRDl^_far_alLsamples  except QO393 which is
14 times CRDL, QO395 which is 3 times CRDL, and Qb396~whlch is 100 times CRDL.
The probability of false negatives  is acceptable  with the exception of the three
samples with  raised detection limits.  False negatives are more likely in the samples
where the detection limits were raised.

-------
                                                                           B-7
 3.5   Pesticides

     The initial and continuing calibrations, and chromatographic quality, with
 exceptions, for pesticides were acceptable.  The matrix spike, matrix spike duplicate,
 surrogate spikes, and holding times were within acceptable limits.

     Pesticide method  blank chromatograms (samples 9206407 and 919403) show the
 presence of an unknown contaminant.

     Seven of the 20 pesticide sample chromatograms were unusable due to poor
 chromatographic quality.  A baseline was not obtained from 3 to  10 minutes into the
 run. Any early eluting pesticides peaks, if present, would have been obscured.
 Samples affected included QO539, 540, 542, 543, 546, 547, and 549.
 Results, especially  for  early eluting pesticides, for these samples should be
 considered suspect.

     The estimated method detection limits for the pesticides fraction were CRDL
 for all samples except sample QO392 which is twice CRDL.  The pesticides results
 should be considered qualitative for all samples except QO539, 540, 541, 543,  546,
 547, and 549.  There is a possible enhanced probability of false negatives for
 pesticides.
III.  Data Usability Summary

4.0  Graohite Furnace Metals
Quantitative:
Semi-quantitative:

Qualitative:
Unreliable:
4.1  TCP Metals

Quantitative:
Semi-quantitative:

Qualitative:

Unreliable:

4.2  Mercury

Quantitative:
Qualitative:
Unreliable:
antimony results with exceptions
arsenic, cadmium,  lead, and selenium results for samples
MQO542, 544, and 551
cadmium and thallium results, both with exceptions; arsenic
results for samples MQO392 and 396; antimony results for
samples MQO394 and 550; and selenium results for samples
MQO393, 394, 396, 536, 537, 540, and 543
arsenic, lead, and selenium results, all with exceptions;
antimony results for MQO395, 545, and  546; cadmium results for
MQO546 and 547
all aluminum, calcium, magnesium, sodium, and vanadium results
all beryllium, chromium, cobalt, iron, nickel, and
potassium, results; zinc results with exceptions
all barium, copper, and  manganese results and zinc results for
samples MQO392, 393, 394, 395, and  396
all silver results
all mercury results with exceptions
mercury results for samples MQO393, 394, and 396
mercury results for samples MQO392 and 395
                                       10

-------
B-8
 4.3  Inorganic and  Indicator Analvtes
 Quantitative:
 Semi-quantitative:
 Qualitative:
 Unreliable:

 4.4  Organic;

 Quantitative:
 Qualitative:
 Unreliable:

 Suspect:
all cyanide, sulfate, sulfide, chloride, and total dissolved  solids
results; TOX results for samples MQO542, 543, and 544;
and POX results for samples MQO393 and 539
all bromide, nitrate nitrogen, nitrite nitrogen, ammonia,
and TOC results; and total  phenol results for samples MQO392,
393, 394, 395, 396, 540, 543, and 548
all POC data; POX results for sample MQO392
total phenols, TOX, and POX results, all  with exceptions
all volatiles results; semivolatiles results with exceptions
pesticides results with exceptions
semivolatile acid fraction results for samples QO396, 543, 549,
and 550
pesticides results for samples QO539, 540, 541, 543, 546, 547,
and 549
 IV.   References
 1.    Organic Analyses:
     CompuChem Laboratories, Inc.
     P.O. Box  12652
     3308 Chapel Hill/Nelson Highway
     Research Triangle Park, NC  27709
     (919) 549-8263
      Inorganic and Indicator Analyses:
                          Centec Laboratories
                          P.O. Box 956
                          2160 Industrial Drive
                          Salem, VA  24153
                          (703) 387-3995

      Quality Control Data Evaluation Report for USPCI, Utah, 10/17/1986, Prepared
      by Lockheed Engineering and Management  Services Company, Inc., for the US
      EPA Hazardous Waste Ground-Water Task Force.

      Draft Inorganic Data Usability Audit  Report and Draft Organic Data Usability
      Report, for the USPCI, Utah site. Prepared  by Laboratory Performance
      Monitoring Group, Lockheed Engineering and Management Services Co., Las
      Vegas, Nevada, for US EPA, EMSL/Las Vegas, 10/21/1986.
                                       11

-------
                                                                                                               B-9
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                                                     IMDLL  D-0
                                            LIMITS OF QUAHT1TATION FO* OMAMIC COMPOUNuS
                                                             USKI
                                                  fantsy Mountain Facility, Utah
                                                             B-ll
                              Linit of
                            Quantitatlon
                               (pg/0
                             Liซit of
                           Qu4ntiUtion
                              (pg/l)
  Volatile Compounds (Purge  & Trap)
  BromojMthane                   20
  Chloronethane                  30
  BroiiodichloroACthane           20
  OibromochloroMthan*           10
  Broftofor*                      10
  Chlorofora                     20
  Carton tetrachloride           10
  Carbon dlsulfide               20
  Chloroethane                   10
  1,1-Oichloroethene             20
  1,2-Oichloroethane             10
  1,1,1-Trichloroethane          20
  1,1,2-Trichloroethane          10
  1,1,2,2-Tetrachloroethane       10
  1,1-Dichloroethane             20
  trans-l,2-Dichloroethene       20
  Trichloroethene                10
  Tetrachloroethene              10
  Methylene chloride             20
  Vinyl chloride                 20
  1,2-Dichloropropane            20
  cis-l,3-0icmoropropene        10
  trans-l,3-Dichloropropene       20
  Benzene                        10
  Chlorobenzene                  10
  Ethyl benzene                   10
  Toluene                        20
  irXylene                       10
  o & p-Xylene                   30
   :etone                        10
   -Butanone                     20
  "2-Hexanone                     20
  4-Methyl-2-pentanone           20
  2-Chloroethyl vinyl ether      20
  Styrene                        10
  Vinyl acetate                  20

  Setii-Volatile Compounds          '

  4-Chloroaniline                20
  2-Nitroaniline                100
  3-Nitroaniline                100
  4-Nitroaniline                100
  3,3'-Oichloroben2idine         40
  Benzyl  alcohol                 20
  1,2-Oichlorobenzene            20
  1,3-Dichlorobenzene            40
  1,4-Oichlorobenzene            20
  1,2,4-Trichlorobenzene         20
 . Hexachlorobenzene             20
  Nitrobenzene                  20
  2,4-Oinitrotoluene             40
  2,6-Dinitrotoluene             20
 , N-Nitrosodiphenylamine         20
  N'Nitrosodipropylamine         20
  bis(2-Chloroethyl)  ether       20
  4-Chlorophenyl  phenvl  ether    20
  4-Bromophenyl  phenyl ether     20
  bi$(2-Chloroisopropyl)  ether   20
  bis(2-Chloroethoxy) aethane    20
  Hexachloroethane              20
^^lexachlorobutadiene           20
^Pซxach1orocyclopentadiene     .30
Seซi-Volatile Compounds  (cont.)

bis(2-Ethylhexyl) phthalate     20
Butyl benzyl  phthalate          20
di-n-8utylphthalate             20
di-n-Octylphthalate             20
Oiethylphthalate                20
Dimethylphthalate               20
Acenaphthene                    20
Acenaphthylene                  20
Anthracene                      20
Benzo(a)anthracene              20
Benzo(b)fluoranthene and/or
  Benzo(k)fluoranthene          20
Benzo(g,h,i)perylene            40
Benzo(a)pyrene                  50
Chrysene                        20
Oibenzo(a,h)anthracene          40
Dibenzofuran                    20
Fluoranthene                    20
Fluorene                        20
Indeno(l,2,3-c,d)pyrene         40
Isophorone                      20
Naphthalene                     20
2-Chloronaphthalene             20
2-Hethylnaphthalene             20
Phenanthrene                    20
Pyrene                          20
Benzoic acid                   100
Phenol                          20
2-Chlorophenol                  20
2,4-Dichlorophenol              20
2,4,5-Tn'chlorophenol          100
2,4,6-Trichlorophenol           20
Pentachlorophenol              100
4-Chloro-3-methylpheno1         20
2-Methylphenol                  20
4-Methylphenol                  20
2,4-Oinethylphenol              20
4,6-Oinitro-2-ซethylphenol     100
2-Nitrophenol                   20
4-Nitrophenol                  100
2,4-Oinitrophenol              100
Pesticides/PCBs
Aldrin
alphซ-BHC
beta-BHC
gaปa-6HC
delta-BHC
Chlordane
4,4'-000
4,4'-DOE
4,4'-OOT
Dieldrin
Endosulfan I
Endosulfan II
Endosulfan sulfate
Endrin
Heptachlor
Heptachlor epoxide
Toxaphene
Methoxychlor
Endrin ketone
PCB-1016
PCB-1221
PCS-1232
PC8-1242
PCS-1248
PCB-1254
PCB-1260
                         Limit of
                       Quantitation
                          (pg/D
  05
  05
  05
  05
  05
  5
  1
  1
  1
0.1
0.05
0.1
0.2
0.1
0.05
0.05
1
0.5
0.2
0.
0.
0.
0.
0.
1
1
.5
.5
.5
.5
.5
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