38
CAMERON S. DUNNAN/2 KEY PROJECTS (Continued) Authored organic and inorganic data validation report, in accordance with USEPA Functional Guidelines, for a non-regulated environmental site in Dos Campos, Brazil. Performed contract compliance screening and organic/inorganic data assessments and validations, in accordance with USEPA Region II protocols, for a chemical production facility in Morristown, New Jersey. Authored multiple organic and inorganic data validation reports, in accordance with USEPA Region III guidelines, for ground water, soil, and sediment samples from a landfill in South Whitehall Township, Pennsylvania. Managed extensive historical database for ground-water chemistry of drinking water wells in St. Thomas, U.S. Virgin Islands. Established communication link for electronic transfer of project data from laboratory. Created database application for tracking and scheduling of laboratory analyses and validation/management in support of current site investigations. Implemented database application forcomparing applicable regulatory limits with sample- specific contamination. 3/92 AR300237 GERAGHTY & MILLER,INC.

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CAMERON S. DUNNAN/2

KEY PROJECTS (Continued)

Authored organic and inorganic data validation report, in accordance with USEPAFunctional Guidelines, for a non-regulated environmental site in Dos Campos, Brazil.

Performed contract compliance screening and organic/inorganic data assessments andvalidations, in accordance with USEPA Region II protocols, for a chemical productionfacility in Morristown, New Jersey.

Authored multiple organic and inorganic data validation reports, in accordance withUSEPA Region III guidelines, for ground water, soil, and sediment samples from alandfill in South Whitehall Township, Pennsylvania.

Managed extensive historical database for ground-water chemistry of drinking water wellsin St. Thomas, U.S. Virgin Islands.

Established communication link for electronic transfer of project data from laboratory.

Created database application for tracking and scheduling of laboratory analyses andvalidation/management in support of current site investigations.

Implemented database application for comparing applicable regulatory limits with sample-specific contamination.

3/92

AR300237GERAGHTY & MILLER, INC.

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UMA PARASAR

Scientist

CREDENTIALS/REGISTRATIONM.S. Environmental Science, Toxicology, New Jersey Institute of Technology, 1990B.S. Environmental Science, Chemistry, Botany, St. Josephs College, Bangalore, India,

. 198840-Hour OSHA Training Course

PROFESSIONAL AFFILIATIONSAmerican Chemical Society

FIELDS OF SPECIALIZATION- Data validation.- Data management.- Bioremediation of incinerator ash.- EP toxicity and TCLP tests.- Risk assessments.- Environmental regulations.- Field sampling.

EXPERIENCE SUMMARYAt Geraghty & Miller, Ms. Parasar performs data validation and data management. She hasalso worked on field investigations where she sampled soil, ground-water, and sediment, andsupervised the installation of monitoring wells. Prior to joining Geraghty & Miller, Ms.Parasar performed laboratory research and worked as an adjunct professor at RutgersUniversity and as a teaching assistant at the New Jersey Institute of Technology.

KEY PROJECTS- Participated in field activities related to the New Jersey Environmental Cleanup

Responsibility Act (ECRA) in Boonton, New Jersey. Project included installingmonitoring wells and deep soil borings and collection of soil and water samples.

- Performed preliminary assessment to evaluate overall data quality for an ECRA facilityin Garfield, New Jersey.

- Performed a preliminary data assessment in support of the soil and ground-waterinvestigations carried out at a trichloroethylene-contaminated site in Hillside, New Jersey.

- Performed the data validation for a chromium remediation project in Hudson County,New Jersey, using the New Jersey Department of Environmental Protection and Energy(NJDEPE) regulations.

GERAGHTY & MILLER, INC.

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UMA PARASAR/2

KEY PROJECTS (Continued)

- Performed data validation in support of an ECRA investigation at a service station in theU.S. Virgin Islands using United States Environmental Protection Agency (USEPA),Region II guidelines.

- Performed data validation to assess data quality under a Resource Conservation andRecovery Act (RCRA) investigation at an oil refinery in Puerto Rico, using USEPARegion II guidelines.

- Performed the preliminary data validation on residential well water samples collectednear a municipal sanitary landfill in Pennsylvania, using USEPA Region III guidelines.

- Performed the quarterly renewals for the NJPDES permits for monitoring wells at anECRA site in Boonton, New Jersey.

3/92

GERAGHTY & MILLER, INC. ^ " J (J 0 2 3 9

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APPENDIX C

ANALYTICAL METHOD SUMMARIES

GERAGHTY & MILLER, INC. $ R 3 Q 0 2 if i i

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APPENDIX C

ANALYTICAL METHOD SUMMARIES

Appendix C is a summary of analytical methodologies that will be used by EnsecoEast or their subcontractors in support of the RI/FS at the Dublin TCE Site, Dublin,Pennsylvania.

VOLATILE ORGANIC COMPOUNDS

Volatile organic compounds (VOCs) will be analyzed using various U.S.Environmental Protection Agency (USEPA) analytical methods based on the RI/FSrequirements, the data quality objectives and the sample matrices.

USEPA Method 524.2 Revision 3.0

USEPA Method 524.2 (Revision 3.0) is a general purpose method for theidentification and simultaneous measurement of purgeable VOCs in finished drinking water,raw source water, or drinking water in any treatment stage. VOCs are determined bypurging 25 milliliters (ml) of sample and analyzing by capillary column gaschromatography/mass spectrometry (GC/MS). The method detection limits are compound-and instrument-dependent and vary from approximately 0.02 to 0.35 micrograms per liter(ug/L). This method has been modified for the quantitation of target compound list (TCL)VOCs. The surrogate compounds normally used for USEPA Method 524.2 will besubstituted with the TCL VOC surrogate compounds in accordance with the USEPA March1990 contract laboratory program (CLP) VOC protocols.

USEPA Method 8240

USEPA Method 8240 is used to determine VOCs in a variety of solid waste matricesincluding ground waters, aqueous sludges, waste solvents, oily waste, soils, and sediments.

GERAGHTY & MILLER, INC. A R 3 0 0 '£ k

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C-2

This method is based upon a purge-and-trap GC/MS procedure. The practical quantitationlimit (PQL) of Method 8240 is approximately 5 micrograms per kilogram (ug/kg) forsoil/sediment samples (wet weight) and 5 ug/L for water samples.

USEPA March 1990 Contract Laboratory Program Routine Analytical ServicesStatement of Work

The USEPA March 1990 CLP routine analytical services (RAS) statement of work(SOW) protocols cover the determination of the TCL VOCs and include an optionalhexadecane screening procedure. The extract is screened on a gas chromatograph/flameionization detector (GC/FID). to determine the approximate concentration of organic

constituents in the sample. The actual analysis is based on a purge-and-trap GC/MSmethod. For soil/sediment samples, the purge device is heated. This method is based onUSEPA Method 624.

USEPA Method TO-14

USEPA Method TO-14 is used to determine VOCs in ambient air using SUMMA™passivated canister sampling and GC/MS analysis in the scan mode.

BASE NEUTRAL AND ACID EXTRACTABLE SEMIVOLATILEORGANIC COMPOUNDS

Base neutral and acid extractable (BNA) semivolatile organic compounds will beanalyzed using the USEPA March 1990 CLP RAS SOW protocols.

GERAGHTY & MILLER, INC.

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C-3

USEPA March 1990 Contract Laboratory Program Routine Analytical Services

Statement of Work

The USEPA March 1990 CLP RAS SOW method involves solvent extraction of thesample matrix, characterization by GC/FID screening to determine the appropriateanalytical protocol to be used, and GC/MS analysis to determine the TCL constituent levels

present in the sample. This method is based on USEPA Method 625.

PESTICIDES AND POLYCHLORINATED BIPHENYLS

Pesticides and polychlorinated biphenyls (PCBs) will be analyzed using the USEPAMarch 1990 CLP RAS SOW protocols.

USEPA March 1990 Contract Laboratory Program Routine Analytical ServicesStatement of Work

The USEPA March 1990 CLP RAS SOW protocols are designed to analyze water,sediment, and soil from hazardous waste sites to determine the presence and concentrationof the chlorinated pesticides and PCBs found on the TCL. The method can be used fordetermining analyte concentrations in the range from the contract required quantitationlimits (CRQL) to one million times the CRQL in these matrices. The method is based onUSEPA Method 608.

METALS

Target metals will be analyzed using the USEPA March 1990 CLP RAS SOWprotocols.

GERAGHTY & MILLER, INC. ^ L'" J

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C-4

USEPA March 1990 Contract Laboratory Program Routine Analytical ServicesStatement of Work

The USEPA March 1990 CLP RAS SOW protocols specify use of analytical methodsfrom Methods of Chemical Analysis of Water and Wastes, as modified for the CLP.Instrumental techniques include analyses by inductively coupled plasma-atomic emissionspectrometry (ICP-AES), graphite furnace atomic absorption, and cold vapor atomicabsorption for 23 metals of the target analyte list (TAL).

TREATABILITY

Analytical results of several parameters will be used collectively to determine theeffectiveness of the treatment system design. These have been designated as treatabilityparameters in this QAPP and consist of the following determinations: alkalinity, calcium,iron, magnesium, manganese, hardness, total dissolved solids, and total suspended solids.

Alkalinity

Alkalinity is calculated by analysis of an unaltered sample that is titrated to anelectronictrically determined endpoint of pH 4.5.

Metals

Concentrations of calcium, iron, magnesium, and manganese will be determined byICP-AES after appropriate sample preparation.

Hardness

Water hardness is calculated using the calcium and magnesium concentrations thatare determined by ICP-AES analysis.

/1R3002HGERAGHTY & MILLER, INC.

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C-5

Total Dissolved Solids

A \vell-mked sample is filtered through a glass fiber filter and the filtrate isevaporated and dried to a constant weight. The weight of the remaining residue is reportedas total dissolved solids (TDS) in milligrams per liter (mg/L).

Total Suspended Solids

A well-mixed sample is filtered through a glass fiber filter and the residue retainedon the filter is dried to a constant weight. The weight of the remaining residue is reportedas total suspended solids (TSS) in mg/L.

WET CHEMISTRY/PHYSICAL PROPERTIES

Various chemical determinations and physical tests will be performed to classify thetransport characteristics of the sediment samples. These include analyses for total organiccarbon and grain-size determinations.

Total Organic Carbon

A sample is oxidized with potassium chromate in the presence of sulfuric acid. Theexcess chromate is determined by titration with a standard iron sulfate solution. Thequantity of substances oxidized is calculated from the amount of chromate that is reducedby the titrant. *

Grain Size

Grain size is performed in accordance with ASTM D422, D4318, and D2487-85,which classify soils after particle size is determined through sieve analysis.#NJ14301-QAPPT/APP-B.WP

GERAGHTY & MILLER, INC.

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APPENDIX D

USEPA REGION IIIORGANIC AND INORGANIC DATA VALIDATION REPORTING FORMS

HR30G2U6GERAGHTY & MILLER, INC.

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•s |Sg£

1 ' 11r '-33DATA SUMMARY FORM: VOLATILES 1

WATER SAMPLES

(ug/L)

Site

Name:

Case#:

Sampling Date(

s):To

calcu

late s

ample q

uai

(CROL'Di

Sample No

.Dilution Fa

ctor

Location

CRQL

Compound'

| Chloromethane

0

j0

| 'Vinyl C

hloride

0

| Chloroethane

2

•Methylaie

Chloride

1 Acetone

0

[ Carbon

Disulfide

•1,1-Dichtaroethene

1 1,1-Dfahbroethane

| 'Total 1,2-Dichloroethene

| Chloroform

| '1,2-Dichloroethane

| *2-Butanone

0

| '1,1,1-TrfchIoroethane

vn

| 'Carbon

Tetraihloride

11>,

0

| Bromodchloromethane

! ( = Contract Re

quired Quantitation Limit

*Action Level E

xists

See Narrative f

or Code Definitions

CD

^i

revise

d 07/90

CD ro jr-

Page 13: CAMERON S. DUNNAN/2 - Superfund Records Collections · PDF fileCAMERON S. DUNNAN/2 KEY ... Managed extensive historical database for ground-water chemistry of drinking ... - Performed

i

C/3wH

9 wg

1 J11 ^

1

sii/3 Z

t/a

I.3

I

. .

a

'R 2

ititat

ion li

lution

Fac

0"*<U ,_)n°SD

11

-

c

I

Dikation Fa

ctor 1

1(3§

CLs1.uQ

3s— 13-Dchloroptopane

'rbhloroethene

~) ibromochloromethane

w

1,1,2-Trehlorethane

c

IX

IC

.uQ

T1 Sr

omoform

c

IvsSi

a

,-Hacanone

'o

Tetrachloroethene

l,l,2,2-Tetra;hlorotthane

1

<uc

g 1<u

1I

AR3002U8

Page 14: CAMERON S. DUNNAN/2 - Superfund Records Collections · PDF fileCAMERON S. DUNNAN/2 KEY ... Managed extensive historical database for ground-water chemistry of drinking ... - Performed

0}•DATA SUMMARY

FORM: V

OLATILES

1

SOIL SAMPLES

(ug/Kg)

Site

Name:

Case#:

Sampling Date(s):

To ca

lculat

e sample q

uantitation l

imit:

rCROL * Dilution Fa

ctor VfYlOO - % mo

istureVlOOl

Sample No

.Ditition Fa

ctor

% Mo

isture

Location

CRQL

Compound

Chloromethane

o

Bromometbane

o

| 'Vinyl Chloride

0

| Chloroethane

0

| 'Methylene Chloride

VO

,o

| CarbonDisulfide

[ '1,1-Dichloroetbene

I 1,1 -

D chloroethane

'Total 1,

2-Dichloroethene

| Chlorofonn

V>

| *1,2-D chloroethane

| *2-Butanone

o

•1,1,1-Trbhloroethane

•Carbon Tetrxhioride

V

1Oi— t

[ Bromodchloromethane

i\ ft 3<

Definitions

vised 07/90

e for

Na

Page 15: CAMERON S. DUNNAN/2 - Superfund Records Collections · PDF fileCAMERON S. DUNNAN/2 KEY ... Managed extensive historical database for ground-water chemistry of drinking ... - Performed

o

>

onW

&g"B.

ate sa

mple

quantitation li

mit:

3rW100-%moistureVian

To ca

lcul

( CROL*

Dilution Fa

ct*Sample No

.Dilation Fa

ctor

% Mo

isture

Location

CRQL

Compound

ojiO.S

2.si

3r-**

in

1eD-

1.c.uQi

I(3 Tr

fchloroethene

D ibromochloromethane

1,1,2-Trichlorethane

uiOJCO*

11zsJZ,uQ

T(- Br

omoform

OJ

11

"a

1

g

2-Heranone

c

•Tetrxhioroethene

1,1,2,2 -

Tetrachloroethane

•Toluene

•Chlorobenzene

•Ethylbenzene

*

">,X

v> M Q, = Contract Re

quired Qu

antitation Limit

• See N

arrative fo

r Code

Definitions

CD

4ABj|f

t2 rev

ised 07/90

fXJ

Page 16: CAMERON S. DUNNAN/2 - Superfund Records Collections · PDF fileCAMERON S. DUNNAN/2 KEY ... Managed extensive historical database for ground-water chemistry of drinking ... - Performed

rt. s -,-, «t" • ••• -f

j

t — i

55

S i-C &Z)

P nq• C t

i

CD

K Z

s

ug.f"fi.

ua

| s11jj-c

1SE2

-

Sample No.

Dilation Fa

ctor

Location

IaBd_J

If

O

1o

•bis(2-Chloroethyl)ether

o

2-Chlorophenol

o

•1,3-Dichlorobenzene

o

*l,4-Dichlorobenzene

o

Benzyl Ab

ohol

0

1,2— Dchlorobenzene

0

2-Methylphenol

o

_to

a..i

6S0

4-Methylphenol

0

.1

11•51

'EiZo

Hexachloroethane

0

Nitrobenzene

0

o.co.J0

1 2-Nitrophenol

0

2,4-Dimethylphenol

0

BenzocAcid

0

bis(2-Chloroethoxy)methane

o|

t

[ 2,4-Dfahlorophenol

0

fi

' 1,2,4-Trichlorobenzene

c

3

Naphthalene

0

.1

1

02,

&3 o0 .?£ l T

ieDefinit

revise

d 0'

6i—i

arrati

ve fc

Z

JS

31

13h— 1

I

•*— >

g .1•£*

= Contract Re

quired Qi

•T4/bnasfrl

Sf

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*S 'go

1 P1 11

'g 3

§-Qa"**-£ i — 'o-OE p£Sy

38

^

« a>

0 1 ^ * ' . •*fe ^ b>" S-S-

i ^OO

1

a

f"B-,S

i5 ^

ll d

0>n.

Dilation Fa

ctor

Lxation

11e6j

H

Hexachlorobutadiene

o

.cji,

H11S°eo

2 - Methy I

naphthalene

o

Hexachlorccjc l

opentadiene

o

2,4,6-Trichlorophenoi

o

2,4,5-Trichlorophenol

o

2-Chloronaphthalene

o

2-Nkroaniline

o

4j

1|1c<=

<usfflO

2,6-Dinitrotobene

o

3-Nitroaniline

o

11o

|Q

r-f

o

c8iz1e

Dibenzofuran

o

2,4-Dinitrotobene

o

Jli131J3aI5OJ5<=>

S3•S

1

S6io

Fluorene

a

4-Nitroaniline

/

I11§.3Q1

IFn\ w

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J «^o 3 o1 -£1 gfc

§> 1|P"1 '-S £

CT<*

1§a "~CO

DATA SUMMARY FORM: BNAS 3

WATER SAMPLES

(ug/L)

Site

Name:

Case#:

Sampling Date(s):

To ca

lcul

Sample No

.Dilltion Fa

ctor

Location

CRQL

Compound

N -Nitrosodiphenylaoiine

o

4— Bromophenyl-phenylether

o

S

JD

2

o

a.

11o

|o

Anthracene

o

Di-n-butyfcbthalate

o

Fluoranthene

o o

Butylbenzylphthalate

o

3,3'-Dicbk»robenzidine

o

*

Benzo(a)anthracene

o o

bis(2-Ethylhexyl)phthalate

o

3a1IiQo

Benzo(b)fluoranthene

i

Benzo(k)fluoranthene

81s In

deno(l,2,3-cd)pyrene

s Dibenz(a,h)antbracene

(J1i25;3

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<4-lO

U£PiSit

eName:

CaTo ca

lculat

e sample q

uantitation l

imit:

CCROL * Dilution Facto

r1) / (d - % moistureVKXtt

Sample No

.Dibtion F

actor

% Mo

isture

Location

CRQL

Compound

1

§

bis(2-Chloroethyl)ether

CO

I.9

§

*1,3 -D

bhlorobenzene

&en

*l,4-Dbhlorobenzene

13

Benzyl Ab

ohol

9

1,2-Dbhlorobenzene

§

1

t1

cr

11

1CL.iefiIB

§

is1

8

11a1

I

"c1&.tf

11ss

c

|iz

S

1

tuC

1

fl

ccOJ

_c

IQ

^

Benzob

Acid

bi$(2-Chloroethoxy)rnethane

l?|l

a1a2i.uQ1

i

1,2,4-Trbhlorobenzene

iV.

a11

tj

t— Choroaniline

oo

"E.I ———————————————————

o

<u

,o

CO

c

iOS

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DATA SUMMARY FORM: BNAS 2

SOIL SAMPLES

(ug/Kg)

Site

.Name:

Case#:

Sampling Date(s):

To ca

lculat

e sample q

uantitation l

imit:

CCROL *

Dilution Fa

ctor

/ fd

OO - % mo

istureVlOm

*

Sample No.

Dilition Factor

% Mo

isture

Location

CRQL

Compound

Hexachlorobutadiene

S

D.

|-u81fO1££51• t

^

| 2-Methylnaphthalene

S

<u.§

J"|5

XSfO

[ 2,4,6-TrichtophenoI

^

| 2,4,5-Trichlorophenol

1

2-Ch!oronaphthalene

g

2-Nitroaniline

1

5J£J:0>

58

8??JZ

RCO

trotobene

1*0M

S!CO

ze i

1

x:J3

1g

2.5Q•< "

— H

4-Nitrophenol

—H

C

JQ

§

[ 2,4-Dinitrotohene

S

Diethylphthalate

g

4-Chlorophenyl-phenylether

H

Fhorene

fi

4-Nitroaniline

4,6-Dinitro-2-methylphenol

SE

1-<U

aCD

11

|s'§

•s1OS|,^ii ?

300255

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§1

S 11ll•u 1"H.QE o

« r^

DATA SUMMARY FORM: BNAS

3

SOIL SAMPLES

(ug/L)

Site

Name:

Case#:

Sampling Date(

s):Tocalcul

fCROL*

Dilution Fa

ct*Sample No

.Ditltion Fa

ctor

% Mo

isture

Location

CRQL

Compound

N-Nitrosodiphenylamine

8

4-Bromophenyl-phenylether

8

'Hexachlorobenzene

8

'Pentachlorophenol

11c

CU

a

Anthracene

tr

<u

JS>Iic1Q

8

Ftaoranthene

8

S&cu8

^1jIX

8

3,3' -D i

chlorobenzidine

1 Benzo(a)anthraeene

8

I8

a.s1

1aci

8

as-8iciQ

1

Benzo(b)fluoranthene

ff BenzofOfluoranthene

I ffi

r

Indeno(l,2,3-cd)pyrene

r<

Dibenz(a,h)anthracene

<u

•c"

f56

"8

Z

IG

",

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PQOa<Q

noWQ o o

W1-1 >Ju S« §H <en wW Pi

I2

DCO

Qeo

"5,I

*« I 8•" C3 ea33 !Z U

ntitat

ion li

mit:

lution Factor")

To ca

lculate sample qua

f (CRQL * Di

Sample No.

Dilution Factor

Location

CRQL

Compound g

CQ

aj."to

VIoo

OacCO

n«JD

toO

O

IS1

1 'gamma- BHC(Lindane)

W-lo

•Heptachlor

«/>o

o•a<v%

Heptachlor Epoxide

t/i

Endosulfan 1

i

Dieldrin

o

§Q_l•v"o

cs&•0

Endosulfan 11

o0

QQQ

VTT"

oo

Endosulfan

Sulfate

;

oo

SQSr•nf

0

o

*Metboxycblor

o0

! Endrin Ketone

oo

us•5og1nsa

O

o

gamma-Chlordane

X)a

1,

N6

Aroclor-1 S

Aroclor-

MR

Aroclor-

S

Aroclor-1

00Si a

Aroclor-1

os

Aroclor-

1

5R300257L

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WATER SAMPLES

(ug/L)

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revised 07/90

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Name:

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DATA SUMMARY FORM: INORGANICS

SOIL SAMPLES

(mg/Kg)

Site

Name:

Case#:

.

Sampling Date(s):

nit is

affected.

j for specifics.

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| A

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4

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APPENDIX E

QA/QC DATA ASSESSMENT CHECKLISTS

GERAGHTY & MILLER. INC. flR300265

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ORGANIC OA/OC DATA ASSESSMENT CHECKLIST

Project Number:_____________Project Manager:________Project Name/Site:_____________No. of Samples/Matrix:_____

Laboratory:_________________Project/Log-in/SDG No:____Parameter(s)/Method(s):__________________________

DATA ASSESSMENT SUMMARYNotes: 1. Flag major deficiencies/discrepancies; specify parameter and sample

number, if appropriate.2. State not applicable (NA) if not required or if no deviations were

observed.3. Attach substantiating raw data documentation copies, if necessary.

1. Holding times:_____________________________________

2. Blanks:

3. Calibrations:

4. Surrogates:.

5. GC/MS tune and instrument performance:

6. Internal standards:

7. Matrix QC:_

8. Quantitation limits:,

9. Other:

Overall assessment:

Data Reviewer:__________________Date reviewed:.cc: QA officer, Project manager, Project fileNJ14301/qappT/qaform2.wp

GERAGHTY & MILLER, INC.

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Project Number:_____________Project Manager:____Project Name/Site:____________No. of Samples/Matrix:_Laboratory:__________________Project/Log-in/SDG No:.

Parameter(s)/Method(s):______________________

DATA ASSESSMENT SUMMARYNotes: 1. Flag major deficiencies/discrepancies; specify parameter and sample

number, if appropriate.2. State not applicable (NA) if not required or if no deviations were

observed.3. Attach substantiating raw data documentation copies, if necessary.

1. Holding times:__________________

2. Blanks:

3. Calibrations:

4. ICP Interference check standard:

5. Laboratory control sample(s):

6. Matrix QC:_

7. Quantitation limits:

8. Other:

Overall assessment:

Data Reviewer:________:_________Date reviewed:.cc: QA officer, Project manager, Project fileNJ14301/qappTl/qaform.wp

GERAGHTY & MILLER, INC. flR300267

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APPENDIX F

FIELD AUDIT FORM

GERAGHTY & MILLER, INC.

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Page 1 of 3

FIELD AUDIT CHECKLIST

Project___________ Date____________ Time____________

Auditor(s)__________.____________________________________________________

On-site Sampling Personnel_________________________________________

Activity(ies) Audited_________________________________________________

Ground-Water Sampling Observations:

Proper sampling locations?

Residential well samples collected prior to treatment?

Sampling location documented?

Sampling times documented?

Well specifications noted accurately?

Purge volume calculated correctly?

Field filtering for dissolved metals analysis?

Proper measurement of field parameters?

Proper calibration of field instruments anddocumentation?

Dedicated bailer line and/or tubing?

Proper disposal/containment of purge water?

Sampling proceeding from suspected leastcontaminated well to most contaminated?

Sample bottles properly labeled?

Proper containers and preservation used?

Sample bottles filled in correct order?

Volatile sample vials checked for bubbles?

Samples refrigerated/iced immediately after collection?

GERAGHTY<2? MILLER, INC. " " "

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Page 2 of 3

Soil/Sediment Sampling Observations:

Proper sampling locations? _________

Sampling locations documented? _________

Sampling times documented? _______

Dedicated spoons/trowels used? __________

Sample bottles properly labeled? ______

Sampling proceeding from suspected leastcontaminated area to most contaminated area? __________

Sample bottles filled to maximum extent possible? __________

Samples refrigerated/iced immediately after collection? __________

Proper sample selection criteria employed? _________

Proper depth of sample collection? _________

Log (grain size, color, etc.) of material complete and accurate? __________

Air Sampling Observations:

Proper sampling locations? __________

Background sample location free of potentialcontaminant sources? ______________

Vacuum pressure of sample canister at least 28-inchesof mercury before sampling? __________

«

Sample lines flushed prior to sampling? _________

Proper sample period used? _________

Final vacuum pressure of sample canister at least5-inches of mercury after sampling? _________

Initial and final vacuum pressures recorded onsample sheets and tags? _____________

Safety: Ground-Water Soil/Sediment AirSampling Sampling Sampling

Proper level of protective clothing? _____ _____ _____

HASP available? ____ ____ ____

Monitoring equipment available? ____ ____ ____

Monitoring equipment properly calibrated?

Disposable surgical gloves changed betweensample locations? _____

—— ATT30Q270GERAGHTY & MILLER, INC.

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Page 3 of 3

Ground-Water Soil/Sediment AirSampling Sampling Sampling

General:

Collection of appropriate QA/QC samples(trip blank, field, replicate)?

Does the potential for sample cross-contamination existexist based on procedures served?

Proper decontamination procedures followed?

Are employees conducting the investigationin a professional manner?

Sampling objectives understood by personnel?

Are weather conditions affecting sample quality?

Efficient operation of field activities?

Do field personnel have QA/QC manual availablefor reference?

Do field personnel have proper protocolsavailable?

Is work area kept clean, orderly and contamination free?

Are all required supplies available?

Are field forms filled out completely and accurately?

Are chain-of-custody procedures followed?

Audit Summary and Comments:

Recommendations:

Signature:_____________________:_________________ Date:

DV/5cqiudil.fral

GERAGHTY & MILLER, INC.

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APPENDIX G

CORRECTIVE ACTION REPORT

AR300272GERAGHTY & MILLER. INC.

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CORRECTIVE ACTION REPORT(CAR)

Project Number:_______________ Project Manager:.

Project Name:_______________________________

CAR No.:___________________ [ ] Sample Location(s) Affected:

Date: __________________ __________________

Name of Individual Initiating CAR: [ ] Sample ID(s) Affected:

Note: Attach copies of all pertinent documentation, if applicable.

Field and/or Laboratory Observation/Anomaly:

Signature: Date:

Project Manager/Project Officer/QA Officer Management Action:

Signature: Date:

Proposed CAR Review Date/Schedule:

Signature: Date:

Quality Assurance Approval:

Signature: • Date:

Copy To: [ ] Project File [ ] Project Manger [ ] Project Officer

[ ] QA Officer [ ] Client [ ] Agency (specify).OV-1/carfonn

GERAGHTY & MILLER, INC.