United States
 Environmental Protection
 Agency	
Environmental Monitoring
Systems Laboratory
Cincinnati, OH 45268
jj^r
 Research and Development
EPA/600/S4-89/010 Sept. 1989
 Project Summary

 USEPA  Method  Study  36
 SW-846 Methods  8270/3510
 GC/MS  Method  for Semivolatile
 Organics:  Capillary Column
 Technique;  Separately Funnel
 Liquid-Liquid  Extraction
 Kenneth W. Edgell
  An interlaboratory collaborative
study was conducted  on SW-846
Methods 8270/3510 entitled "GC/MS
Method for Semivolatile Organics:
Capillary Column Technique; Separa-
tory Funnel Liquid-Liquid Extraction"
to determine the precision and re-
covery of  59  Semivolatile organic
compounds in reagent water, ground
water and leachate. SW-846 Methods
8270/3510 include instructions for
quality control, sample  preparation,
and analysis by gas chromatography
mass spectrometry (GC/MS).
  The study design was based upon
Youden's  non-repllcate  plan for
collaborative  tests  of analytical
methods. The test waters: reagent
water used as a  control, ground
water, and hazardous waste leachate
were spiked  with 59 Semivolatile
compounds at six concentration
levels (three  Youden pairs). In the
study of SW-846 Methods 8270/3510,
ten laboratories extracted the test
waters with  methylene chloride,
concentrated the extract to 1 mL and
analyzed  the extract for 59
semivolatlle compounds by GC/MS.
The results were analyzed using
USEPA computer programs entitled
"Interlaboratory Method Validation
Study"  (IMVS) which produced
measures of precision and recovery
for the 59 Semivolatile compounds in
each water type and compared  the
performance of the method among
water types.
  The study was conducted under
the  direction  of the Quality Assur-
ance Research Division, Environ-
mental Monitoring Systems Labora-
tory, Cincinnati, OH (EMSL-Clncinnati)
Environmental Protection Agency,
under Contract No.  6803-3254.
Analytical work was completed as of
September 1987. The report covers a
period from September 10, 1986 to
December 21,1987.
  This Project  Summary was devel-
oped by EPA's Environmental Monitor-
ing  Systems Laboratory,  Cincinnati,
OH to announce key findings of  the
research project that is  fully docu-
mented in  a separate report of  the
same title (see  Project Report
ordering information at back).


Introduction
  The Hazardous Waste  Management
Facility Permit  Regulations promulgated
in July, 1982 (40 CFR 265) establishes
performance standards for the monitoring
of ground waters, wastewaters and solid
wastes at hazardous waste sites.  To
facilitate these  standards, chemical and
physical analyses are required to assess
the degree of ground water contamination
at and around the the site. The Manual:

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[Test Methods for Evaluating Solid Waste
Physical  and Chemical  Methods,  (SW-
846),  November 1986,  Third  Edition],
provides  a  unified, up-to-date source of
information  on sampling and analyses
related to  compliance  with Resource
Conservation  and Recovery Act  (RCRA)
regulations. The success of pollution
control activities, particularly  when legal
action is  involved,  depends  upon  the
reliability  of the  data  generated by  the
laboratories, therefore  it is important to
evaluate  the  analytical  methods  fully.
This is best done through interlaboratory
method validation studies.
  The Environmental Monitoring Systems
Laboratory,  Cincinnati,  OH  (EMSL
Cincinnati),  develops/selects  analytical
methods  and  provides quality assurance
(QA)  support  to  agency  programs
involving  water and waste regulations. In
EMSL-Cincinnati, the  responsibility  for
providing  QA  support is  assigned to  the
Quality Assurance  Research  Division
(QARD).  Its QA program is designed to
establish  the   reliability  and legal
defensibility of  waste and  waste data
collected by  the  Agency,  the  state
regulating authorities, the private sector,
and commercial  laboratories  performing
compliance analyses. One of QARD's QA
activities  is to  conduct interlaboratory
method validation  studies to  evaluate
analytical  methods  selected  for  the
Agency's operating programs such as the
Office of Solid Waste.
  This report describes an interlaboratory
method  validation  study  for  SW-846
Method 8270/3510, "GC/MS  Method for
Semivolatile Organics: Capillary  Column
Technique; Separatory  Funnel  Liquid-
Liquid Extraction" for the analyses of 59
semivolatile compounds.
  The  objective of the  study  was to
characterize  the behavior of  Method
8270/3510,  when performed by  multiple
laboratories, in terms of recovery, overall
and single-analyst  precision  and  the
effect of  water type  on recovery  and
precision. The study was conducted  with
the cooperation of  ten  participating
laboratories under  the direction of  the
Quality  Assurance  Research  Division
(QARD),  EMSL-Cincinnati. The Bionetics
Corporation,  as primary contractor to
QARD, was responsible for the collection
and characterization  of  test  waters,
preparation of samples, user  instructions
and report forms, distribution  of samples,
and screening the returned data for gross
errors. The  raw data were  evaluated
statistically  by the QARD using computer
programs  entitled,  "Interlaboratory
Method Validation Studies" (IMVS). Upon
review of  the  draft  report  by EMSL-
Cincinnati,  The  Bionetics  Corporation
prepared the final report.

Description of Study
  Two  SW-846  methods  were
investigated  in this study.  Method 3510
entitled "Separatory Funnel Liquid-Liquid
Extraction"  was used  for the extraction
procedure  and Method 8270 entitled
"GC/MS  Method  for Semivolatile
Organics: Capillary Column Technique"
was used for the determinative step.
  Method 8270 is applicable to Appendix
IX semivolatile compounds.  However, this
study was  limited  to those compounds
not  previously covered under  USEPA
Method Study 30 on  Method  625  a
similar GC/MS method. Method 625  uses
packed  column chromatography while
Method 8270 uses  capillary column
chromatography.  It was  assumed there
would be no significant difference in the
computed  statistics of  the  compounds
covered by  both methods therefore these
organics were not  included  in this study.
Of the remaining 72 compounds, 13  were
unsuitable  for  the  study. Table  2  lists
these compounds  and the  reasons  they
were excluded.  The  remaining 59
compounds were divided into three mixes
for this method study.

Method Summary
  One liter of sample water was extracted
three times  with  60 mL  portions  of
methylene chloride at pH  > 11 then re-
extracted three times with 60 ml portions
of methylene chloride of pH <  2. The
collected extracts  were passed  through
sodium  sulfate then concentrated to 1.0
mL using  a Kuderna-Danish apparatus.
The  concentrated  extracts were injected
into a GC/MS instrument equipped with a
30 meter narrow bore DB-5 fused silica
capillary column or equivalent.

Study Design
  The design  of the study was based
upon Youden's non-replicate design for
collaborative evaluation of analytical
methods. In this design, sample   solu-
tions are prepared in pairs, such that the
analyte  concentrations of the pairs vary
between 5-20% of the mean of the pairs.
For   this  study,  spiking  solution
concentrates of the 59 compounds  were
prepared at six concentration levels,  as
three Youden pairs. The spiking solutions
were divided into three mixes to facilitate
chromatographic  resolution  during  ana-
lyses and to maximize compound  solu-
bility at high concentrate levels. The
ampul concentrates were used to fortify
three water matrices  before  extraction
and   analyses.   Analysts  from  ten
participating laboratories were directed t
extract and analyze each  sample an
report one value for each analyte at eac
concentration level. Analyses in reager
water  were  used to evaluate  th
proficiency of  the  method on  a sampl
free  of  interferences;  analyses  in th
other waters were intended to  reveal th
effects of interferences on the method.
  Each  participating  laboratory  wa
required to analyze a matrix blank and
quality control  sample. Acceptance limit
were provided  with the quality contrc
sample to  give the participating labors
tories their "in-control"  limits.  Eac
laboratory also received a set of standar
solutions   for   use in  preparation  c
calibration  curves.  The cost and  limite
availability  of several of the compound
included  in  this study  necessitated thi
course of action.

Verification  Analyses
  Ampulled samples and standard soli
tions were analyzed by Bionetics persor
nel prior to distribution and compared  t
freshly prepared standards  to verify thi
the solutions were properly prepared an
stable. At the  conclusion of the metho
study,  the ampulled samples  an
standard  solutions  were again  analyze
versus freshly prepared  standards  t
verify the  stability  of  each compoun
throughout the  period of the study.

Selection of the Matrix Waters
  Two waters were  collected  fror
hazardous  waste  sites  for  use in thi
study.  A  ground   water  sample  wa
collected from  a monitoring  well at
sanitary landfill and a leachate sampl
was  collected  from a  closed  cell at
hazardous waste landfill.
  GC/MS  analyses  of the ground wate
sample revealed no background concer
trations of  the 59 analytes  in the stud]
The  leachate sample, on the other han<
contained  phenol   and  phenolic  con-
pounds.  This  matrix  was  ultimatel
diluted to  10%  leachate to reduce th
phenolic  background  concentration  1
levels that would  not saturate th
instrument detector. Interferences  wil
the study compounds were not found.
Selection of Participating
Laboratories
  The Quality  Assurance  Researc
Division (QARD) of EMSL-Cincinnati ws
responsible for the  selection of th
participating laboratories.  As per th
standard  competitive  bid  process, «
abstract  of the scope of  work  wj
announced  in  the   Commerce  Busine:
Daily. Over 100 laboratories  requeste

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the complete request for proposal (RFP)
which included the  evaluation criteria
upon which the offerer would be scored.
  Submitted technical  proposals  were
evaluated  based  upon  laboratory
experience and quality control practices.
Laboratories  whose  proposals  were
acceptable were evaluated  further in a
preaward  performance evaluation study.
The participants selected for the formal
study were the ten laboratories with
acceptable  proposals  who  performed
best in the preaward study.

Results  and Discussion
  The objective of this  study was  to
characterize the performance of SW-B46
Method  8270/3510  in terms of  recovery,
overall precision, single analyst precision
and the  effect of water type on recovery
and precision.
  The calculated  mean recoveries  for
reagent water  indicate that the data
presented  in   this  report  meet the
objectives outlined for  this study.  The
pooled  mean recovery  for  all  58
compounds, excluding  3-methylcholan-
threne, was 77.9% with a standard devia-
tion of 13.3%. Forty-four compounds had
recoveries within one standard  deviation
of  the  pooled  mean.  The  average
recovery of these  44 compounds  was
80.2%  with  a standard  deviation
improving  to 6.3%. The small  improve-
ment in  the pooled mean recovery with a
large  improvement  in the  standard
deviation,  13.3% to 6.3%, illustrates how
tightly the  data are distributed.
  Generally, the ground water matrix had
a  lower mean recovery,  73.5%, than
reagent  water  with 77.9% and slightly
more  variable data with  a standard
deviation  of 16.6%  versus  13.3%  for
reagent  water.  The leachate matrix had
mean  recoveries comparable to reagent
water with 78.9%  and  a  standard
deviation of 14.9%.
  Several  compounds  presented
problems  during the  study thus making
their  regression  equations suspect.
Chlorobenzilate suffered from extremely
poor extraction  efficiency. The  standard
solution  for  3-methylcholanthrene
dehydrogenated  in the  methylene
chloride  causing high sample recoveries.
Three  compounds:  7,12-dimethyl-
benz(a)anthracene,  a,a-dimethyl-
phenethylamine, dibenzo(a,e)pyrene and
tris (2,3-dibromopropyl)  phosphate
suffered  from poor response and erratic
chromatography.
  The  preliminary  stability  studies
revealed that the aromatic amines were
vith the acetone solvent and eluting as
two peaks.  The main peak  was the
aromatic amine and the second was the
reaction  product.  The  amines  were
combining with the acetone and, because
they were stabilized by an aryl  group,
formed stable Schiff bases.
  To prevent this reaction from interfering
with the  8270  analyses,  the aromatic
amines were prepared  as a separate
concentrate (mix 1) with methanol as the
solvent. The Schiff base reaction was not
found  to  occur in this  solvent.  The
remaining compounds were  dissolved
using acetone as the solvent.
  Several compounds were only available
as  a mixture of isomers or as impure
compounds.  They were: di-allate, two
isomers approximately  55% and  45%;
isosafrole, two isomers 80% and  20%;
pronamide with two impurities at 1% and
24% with the  main peak at 75%; 2,3,4,6-
tetrachlorophenol 80% pure with a 20%
impurity   peak;  tris(2,3-dibro-
mopropyl)phosphate 62% pure with two
impurity peaks at 25% and 13%.
  The analytical data, processed through
the IMVS  programs, were subjected  to
three outlier tests, First,  the  Youden's
Laboratory Ranking Procedure was used
to detect and reject data  having a large
systematic  error associated with a
particular  laboratory.  If a  laboratory
reported the majority of their data for a
particular compound-water combination
biased  either  high or low, compared  to
the other laboratories,  this laboratory
would fail the lab ranking  procedure and
all of it's  data would be rejected for that
compound-water combination. Next, zero,
negative  and  non-detected  data  were
rejected.  Finally, the Thompson outlier
test was used to reject individual outliers.
  For the study, the IMVS  computer
programs rejected  17.0% of the 10,620
data points submitted. The percentage of
rejected data did not  vary significantly
among the three water types. Reagent
water had the lowest number of rejected
data, 519 (4.9%), ground water had 695
(6.5%)  rejected data and  leachate  had
595 (5.6%) rejected data.
  The average number of  rejected data
for  all  59 compounds was 30.7.  The
compound with the fewest number  of
rejected data  was safrole at 6 and the
compound with the highest number  of
rejected data  was Chlorobenzilate  at  56.
For purposes  of this report, a compound
was considered to have excessive
outliers if  the  number of rejected data
was greater  than 45 (25% of the  180
submitted data points). Using this guide-
line, only five compounds fell in this cate-
gory: 2-sec-butyl-4,6-dinitrophenol  (49),
methapyrilene  (51), tris(2,3-dibromo-
propyl)phosphate   (51),  1,3,5-
trinitrobenzene (53) and Chlorobenzilate
(56).
  The laboratory ranking  procedure
accounted for  90% of the rejected data
points or 1620 out of the 1809 total data
points rejected.  Thompson's individual
outlier test accounted for the remaining
10% of the rejected data.
  Of the ten laboratories participating in
the study,  Lab 2, Lab  4,  and  Lab 5,
accounted for 46.5% of the rejected data.
Laboratory 2 had the highest number of
rejected data,  297, which  resulted from
their poor performance in the lab ranking
test. Four laboratories (6,8,9, and  10) had
5%  or  less  of  their  submitted  data
rejected.
  The overall  precision,  expressed  as
percent  relative  standard  deviation
(%RSD) was 22% for reagent water, 23%
for the leachate  matrix  and 23% for
ground  water.  These  averages did not
include 3-methylcholanthrene (104%), or
Chlorobenzilate  (68%).  Aniline had the
lowest mean %RSD  across water types
at 9%  while  Chlorobenzilate had  the
highest at 68%.  Nine compounds:  a,a-
dimethylphenethylamine  (29%),  p-
nitroaniline  (34%), methapyrilene (27%),
benzidine (54%),  tris(2,3-dibromo-
propyl)phosphate  (52%), Chlorobenzilate
(68%), 7,12-dimethylbenz(a)anthracene
(50%), dibenzo(a,e)pyrene (49%), and 4-
nitroquinoline-N-oxide  (27%) had mean
overall %RSOs greater than 25% across
all water types.
  The average single-analyst precision,
expressed as  %RSD-SR,  was 10% for
reagent water,  13% for ground water and
10%  for leachate. These precisions,
lower than overall  RSDs, were expected
since within-laboratory  precision was
expected to be  better  than between-
laboratory precision.  The  mean  %RSD-
SR ranged from 6% to 33% for all water
types.
  Twenty-one compounds  showed
statistically  significant matrix  effects in
the ground water sample yet no matrix
effects were found in the leachate.
  Ten of  these  compounds: N-nitro-
somethylethylamine, N-nitrosopyrrolidine,
2-nitroaniline,  4-aminobiphenyl,  benzyl
alcohol, 2-methylphenol, acetophenone,
N-nitrosopiperidine, 2,4,5-trichlorophenol,
and  1,2-dinitrobenzene had  statistically
significant matrix  effects that were  not
considered to be of practical importance.
These compounds  exhibited similar
analyte recoveries for the four highest
sample  concentrates  (Ampuls  1,2,3,4)
whether extracted from reagent water or
ground water.  Their  overall precisions
were also similar. The two lowest  sample
concentrates for  ground water (Ampuls

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5,6),  however,  showed  marked
differences  in recovery versus reagent
water.  The  precisions of these  two
ampuls were also poorer than  those of
reagent water. The regression  equations
generated  by  the  IMVS series of
programs used a weighted  least squares
approach thus  giving low  concentration
samples  equal weight  with  high
concentration  samples.  The  poorer
recoveries with the  low  concentration
samples from  the ground  water  have
adversely affected the statistics  even
though the other concentration  levels
showed  comparable  recoveries to the
reagent  water.  Since these differences
were only observed at the low end of the
concentration range,  the matrix effects
were  not  deemed  of practical   sig-
nificance.  In  all cases  the mean
recoveries for these compounds were no
greater  than 6% different  between
reagent water and ground water.
  One  compound, a,a-dimethylphene-
thylamine,  showed  a  statistically
significant matrix  effect, but was judged
to be of no practical significance.  The
retained data  for  a,a-dimethylphene-
thylamine  in all three  waters were
extremely variable  with the majority of
the %RSDs between 50%-89%, Even the
reagent  water recoveries were  variable.
This extreme  variability  between  the
mean recoveries and the overall precision
makes statistical inference difficult for this
compound.
  The  remaining  ten  compounds:
naphthylamine, benzidine, 3,3'-dimethyl-
benzidine,  4,4'-methylene  bis(2-chloro-
aniline),  3,3'-dimethoxybenzidine,
pronamide,  tris(2,3-dibromopropyl)phos-
phate, kepone, N-nitrosomorpholine, and
4-methylphenol  had  statistically signi-
ficant matrix effects that were  judged to
be of practical importance.  In all cases
ground  water  was  the affected water
type. These compounds had calculated
mean recoveries  which differed more
than 10%  from  reagent water  even
though the precision values were similar.
Also, the  leachate  mean recoveries
paralleled  the  reagent  water  mean
recoveries which  supported the view that
the ground  water matrix was indeed
different from reagent water.

Conclusions
  The  objective  of this study  was to
characterize the performance of SW-846
Methods 8270/3510 in terms of recovery,
overall precision, single analyst precision
and the effect of water types on recovery
and precision. Through the IMVS series
of  computer programs, statistical
analyses of 10,620 analytical values
provided estimates  of recovery  and
precision expressed  as  regression
equations. These equations regressed
recovery against the  true (known) value
and overall precision and single-analyst
precision against mean recovery for each
compound in a  given water type.  The
linear regression equations obtained from
this study, and presented in Table 1, can
be  used to  predict  the  recovery  and
precision of  the compounds studied  at
concentrations in the ranges investigated
in this study.
  For  the  entire  project, the  IMVS
computer programs rejected 17% of the
10,620 data  points  submitted. The
percentage of rejected data did not vary
significantly across water types.
  The pooled mean recovery for 58 com-
pounds, in  reagent water, excluding  3-
methylcholanthrene,  was 77.9% with  a
standard deviation of 13.3%. Three com-
pounds  had  recoveries less  than  60%.
They were chlorobenzilate (26.9%), 7,12-
dimethylbenz(a)anthracene  (51.3%)  and
1,3,5-trinitrobenzene (54.8%).
  The   overall  standard  deviation
expressed as the percent relative stand-
ard deviation (%RSD) ranged from 9%  to
58% across  the three  waters tested,
except  for  3-methylcholanthrene  at
104%.  The single-analyst precision ex-
pressed as the percent relative standard
deviation (%RSD-SR) ranged from 6%  to
33% across the three waters tested. In  all
cases,  the  highest %RSD-SR  (poorest
precision) was associated with the lowest
Youden pair concentration.
  Statistical comparisons of the effect  of
water  type   were performed  on  all
samples.  The ten  compounds  listed
below  were  found to have statistically
significant matrix effects that are  of
practical significance.
  2-Naphthylamine
  Benzidine
  3,3'-Dimethylbenzidine
  4,4'-Methylene bis(2-chloroaniline)
  3,3'-Dimethoxybenzidine
  Pronamide
  Tris(2,3-dibromopropyl)phosphate
  Kepone
  N-Nitrosomorpholine
  4-Methylphenol
  Several compounds did not perform
well during this method validation study.
3-Methylcholanthrene was unstable in the
methylene chloride  standard mixture
provided with  the  study.  All data
generated for  this  compound  were
unusable. Chlorobenzilate had the lowest
recovery, 27%, from reagent water of the
59  compounds tested.  The uniform low
recoveries among all  six concentration
levels point to poor extraction efficiency.
  Compounds exhibiting a high degree c
variability  as  a result of poor chrorru
tography were  7,12-dimethylbenz(a)ar
thracene, 1,3,5-trinitrobenzene, tris(2,3-d
bromopropyl)phosphate,  diber
zo(a,e)pyrene,  benzidine,  3,3'dimethy
benzidine, 3,3'-dimethoxybenzidine, an
4-nitroquinoline-N-oxide.
  Seven  compounds:  N-nitrosodi-r
butylamine,  1,2-diphenylhydrazine,  2
methylnaphthalene,  1,2,4,5-tetrachlorc
benzene,  dibenzofuran,  dihydrosafrol
and safrole appeared to have  saturate
the detector at the highest Youden cor
centration  samples as indicated by low(
mean  recoveries for the  high concentri
tion samples and uniform recoveries f<
the middle  and low  concentratio
samples.

Recommendations
  SW-846 Methods 8270/3510 ar
recommended  for  the analyses  <
Appendix  IX  compounds  with th
exception of the analytes listed in Table
and with the following observations.
  * The strongly  acidic  and basic cor
    ditions  encountered  during th
    extraction procedure were postulate
    to have  caused chlorobenzilati
    methylmethane  sulfonate, N-nitr(
    somorpholine, hexachloroproper
    and 7,12-dimethylbenz(a)anthracr
    to have  poor extraction efficiencie
    Milder extraction conditions  ma
    improve  extraction  recoveries f<
    these compounds.
  * Stability  studies  revealed th
    aromatic amines were reacting wi
    the solvent,  acetone, to form Sch
    bases. Changing  the solvent to metl
    anol  remedied the  immedial
    problem but this situation should  t
    addressed in  the final method writ
    up.
  * 3-Methylcholanthrene (molecul;
    weight  268)  dehydrogenated
    methylene  chloride  to  form
    compound whose molecular  weig
    was 266. The causes of this reactic
    have  not  been  investigate!
    Quantitation  by  GC/MS  is m
    possible when a compound's stru
    ture changes  in standard solutio
    Further  analytical work is  recon
    mended to examine this  reactio
    Analysts  should  be alerted  to th
    situation in the final method write-uf
  * SW-846 Method 8270  recommen<
    use of a DB-5 fused silica  colun
    with a film thickness of 1.0 um. Tl
    preliminary analytical  wor
    performed under another  contrat
    used  DB-5  column  with  a fil
    thickness  of  2.5  um.  Furth

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    analytical work is recommended to
    determine which film thickness would
    offer the greater advantages.


Table 1.      Study 36,SW 846 Method 8270,  Semi-Volatiles,  GC-MS Weighted Linear Regression Equations  for Mean
             Recovery and Precision (in UG!L)




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M i-4 H H
H «€ ftf B*
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-------
Table 1.
(Continued)
  I
  H
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H
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-------
Table 1.
(Continued)
H
X
H
ft
X
H
X
u
X
X
H
    o
    CO

co in so
• sO CO
N . .
3- CO
i m
+ i
x
co X 0
3- CO 31
ca •- a
• — ca
o - -
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II
H H
BC
V> VJ X







r- 3- «-

r- • .
m o
i
+ i
x
3- X U
in m 3
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o o

n n

w « x






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sO CO
1 •-
+ 1
x
r- x o
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o - •
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ii
n n

V) V) X




r- m —
• •- 3-
3
3 m
i
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x
ca X U
CO N sO

• 0 CO
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II
II II

to in x


x
o
H
V3
H
U
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PC X
ft. O
H
H tO
PC M H X
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X X BC >
X X ft. O
x o
H t »9 H
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0 0 PC X
X X W X
PC tO 0 E

ca co r-

3- • •
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X
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H
U H
PC
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+
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X
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ca co co
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BC
v» vi x





o ro —
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m x u
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ch o o
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(T)
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i

X
so X U
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to to x


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X
ca x U

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n
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r-
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•» . .
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1
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PC
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• co r-
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x
r- x w
in P" ^

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o o
II
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PC
W W X


X
o
M

M
U
H
PC X
ft. O
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co •- en
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PC
w n x




ca
d CO —
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o o
1
1 +
X
P» X U
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• — CO
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0 O
II
II II
BC
VI Vt X




co co ca
• co m
o • •
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1 ^
+• 1
X
ca x o
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ca co d
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0 • •
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H
It II
BC
to to x


X
o
H
to
HI
U
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BC X
ft.

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to x
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1
1 +
X
co X U
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o • •
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n
M u
PC
10 (0 X




so r- co

3 • •
ca CO

+ i
X
m x u
m o so
— 3- r-
• 3 m
o • •
0 O
II
II II
PC
to to x


X
o
H
V)
H
U
W
PC X
ft. O
HI
H VI
V) H X
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X PC >
X ft. O
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x hi .J PC
ac *4 x
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H
X

O
X U
o
H 1
H
X PC
PC H
H M
X E
H 3
U X
0 H
(j (5

H V)
X V)
H M
E
PC
X O
PC K X
H PC
> M X
OS E
U t-a E
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PC > V)
X M H
X 5> (9
M PC X
EH n
II I) H
X O

-------
Table 2.     RCRA Appendix IX Analytes not Included in Method 8270
	Compound	Reason for Exclusion from Study
             p-Benzoquinone

               Benzenethiol

            Pentachloroethane


                Resorcinol

        Hexachlorocyclopentadiene


            p-Naphthoqumone

                 Aramite



             Hexachlorophene


           Dibenzo (a,h) pyrene


           Dibenzo (a,i) pyrene


          n-Nitrosodimethylamine


             1-Naphthylamine

            Phthalic anhydride
      No recovery at 20 and 600 ppb.

      Unstable in methanol or acetone

 Decomposes to tetrachloroethene with less
       than 2% recovery at 600 ppb.

      No recovery at 20 and 600 ppb.

   Unstable by themal decomposition and
             solvent reactivity

      No recovery at 20 and 600 ppb.

 No recovery at 50 ppb. 6 % recovery at 600
  ppb. Four peaks are produced from 96%
              pure material.

 No recovery at 50 ppb. 18% recovery at 600
                  ppb.

Insoluble in spiking solvents and commercially
               unavailable.

    No recovery at 50 ppb. Detection limit
          approximately 150 ppb.

    Compound coelutes with solvent 30%
           recovery at 10 ppb.

         20% recovery at  10 ppb.

          No recovery at 100 ppb.
                                        10

-------
  Kenneth W. Edgell is with The Bionetics Corporation, Cincinnati, OH 45246.
  Raymond J. Wesselman is the EPA Project Officer (see below).
  The  complete report, entitled "USEPA Method  Study  36 SW-846  Methods
        8270/3510 GC/MS Method for Semivolatile  Organics: Capillary Column
        Technique; Separatory Funnel Liquid-Liquid Extraction," (Order No. PB 89-
        190 581J AS; Cost:  $28.95, subject to change) will be available only from:
            National Technical Information Service
            5285 Port Royal Road
            Springfield, VA 22161
            Telephone: 703-487-4650
  The EPA Project Officer can be contacted at:
            Environmental Monitoring Systems Laboratory
            U.S. Environmental Protection Agency
            Cincinnati,  OH 45268
United States
Environmental Protection
Agency
Center for Environmental Research
Information
Cincinnati OH 45268
      BULK RATE
POSTAGE & FEES PAI
         EPA
   PERMIT No. G-35
Official Business
Penalty for Private Use $300
EPA/600/S4-89/010

-------