United States
                   Environmental Protection
                   Agency
Atmospheric Research and
Exposure Assessment Laboratory
Research Triangle Park,  NC 27711
                   Research and Development
EPA/600/SR-94/113  January 1995
& EPA      Project Summary
                   Field  Test of a  Generic  Method
                   For Halogenated  Hydrocarbons:
                   A VOST Test at a Chemical
                   Manufacturing  Facility

                   J.F. McGaughey, J.T. Bursey, and R.G. Merrill
                     Laboratory evaluation  studies were
                   performed for the volatile halogenated
                   organic compounds (VHOCs) listed in
                   Title III of the Clean Air Act Amend-
                   ments (CAAA) of 1990  to determine
                   chromatographic retention times, recov-
                   eries from sorbent, and method detec-
                   tion limits, as well as to design (where
                   necessary), construct, and evaluate dy-
                   namic spiking  equipment and proce-
                   dures for VOST. An initial field evalua-
                   tion study was conducted for the VOST
                   (SW-846 sampling Method 0030,  ana-
                   lytical Method 5041) with dynamic spik-
                   ing of VHOCs. A chemical manufactur-
                   ing facility  was selected  as  a second
                   test site. The presence of low levels of
                   some of the compounds of interest was
                   established by the VOST analysis of
                   samples collected during a presurvey.
                   For the field evaluation study, qua-
                   druple trains were operated from 4 col-
                   located sampling probes, with 2  dy-
                   namically-spiked trains and 2 unspiked
                   trains. A sampling scheme to meet the
                   requirements of method evaluation was
                   designed statistically (following  the
                   guidelines for  EPA Method  301), and
                   the data were evaluated statistically. Of
                   23 VHOCs  tested, the VOST showed
                   acceptable  performance  with  respect
                   to recovery and precision for 17.
                     This Project Summary was developed
                   by EPA's Atmospheric Research and
                   Exposure Assessment Laboratory, Re-
                   search  Triangle Park, NC, to announce
                   key findings of the  research project
                   that is fully documented  in a separate
                   report of the same  title (see Project
                   Report ordering information at back).
Introduction
  The validation of a method for a par-
ticular analyte or group of analytes means
that the performance of the methodology
for these analytes has  been established
and demonstrated through  field  tests at
the  type of source category of  interest,
and that the precision  and bias of the
method have been established experimen-
tally. The U. S. EPA, under the authority
of Title III of the CAAA  of 1990,  required
the identification and/or validation of sam-
pling and analytical methods  for  the
VHOCs listed in Table  1. The candidate
method is VOST, which consists of SW-
846 Sampling Method 0030 and  SW-846
Analytical Method 5040  or 5041. EPA de-
termined that the VOST method should
first be evaluated in a laboratory  environ-
ment to establish the veracity of the spik-
ing procedure and the potential applicabil-
ity of the analytical procedures for  the
compounds listed in Table 1.
  The VOST was  evaluated at a coal-
fired power plant using  quadruple VOST
trains sampling from 4 collocated sam-
pling probes to provide further verification
of the dynamic spiking methodology in a
non-laboratory environment and to assess
the  added effect of sampling a combus-
tion matrix upon the performance of the
methodology. Data  obtained in  the first
field evaluation showed that the VOST did
not perform acceptably for all of the can-
didate analytes. The methodology was not
expected to show acceptable performance
for all of the candidate  analytes  listed in
Table 1, but all of the candidate analytes
were included in the testing to  demon-
strate definitively when  the  methodology

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would  not perform  well  and to  provide
quantitative data to assess  method  per-
formance.  Three  of  the  candidate ana-
lytes could not be analyzed by the VOST
analytical  methodology:  epichlorohydrin,
bis(chloromethyl) ether, and  chloromethyl
methyl ether. These 3 compounds are po-
lar, water-soluble, and very reactive, so
they either could not be purged from the
water or reacted with the water.
  A second field evaluation study  was
conducted at a  chemical manufacturing
facility where chemical waste was inciner-
ated. Dynamic spiking of the analytes listed
in  Table"! was performed, using 4 collo-
cated sampling probes with 4 similar VOST
trains. The guidelines of EPA Method 301
were  used to design the sampling  strat-
egy to ensure that adequate samples were
available for statistical  evaluation of bias
and precision.

Procedure
  The objective  of this program  was to
perform a  second field evaluation of the
VOST method (sampling method SW-846
Method 0030; analytical method, SW-846
Method 5041) at a chemical manufactur-
ing facility that incinerated chemical waste,
to allow the collection of sufficient data to
be able to establish the bias and precision
of the method  for the VHOCs  listed  in
Title III of the CAAAof 1990.
  To achieve this  objective,  a field test
site was  selected to allow access for the
quadruple sampling trains required for test-
ing,  with  4 collocated  sampling  probes.
Collection and evaluation of the  data fol-
lowed one of the acceptable approaches
detailed in EPA Method 301: dynamic ana-
lyte  spiking. The  criteria for acceptable
performance of the method for an analyte
are recovery within the  range  of 50%  to
150% with  precision  (expressed  as per-
cent relative standard deviation  of repli-
cate determinations) of 50 or less.
  Sampling was performed by withdraw-
ing gas  from  a single  port  in the  stack
through a Quad probe,  then  directing the
sampled  gas simultaneously to 4 similar
VOST sampling trains.  The  Quad probe
consists  of  4 heated  probes that can be
inserted  into the stack as one unit. The
front end of the Quad  probe  was posi-
   tioned  in the center of the stack and re-
   mained in that location during each  day of
   testing. No traverse of the stack was per-
   formed with  the  Quad  probe.  The  true
   concentrations  of the components  of the
   stack gas were of no interest to this pro-
   gram as  long  as any quantities  of the
   compounds of interest were equal for each
   train. For VOST sampling during the field
   evaluation, two  of the trains of each Quad
   run were dynamically spiked and two were
   unspiked. Sampling  procedures  followed
   Method 0030.
     Dynamic  spiking  of candidate  VOST
   compounds was performed  using a com-
   pressed  gas  cylinder  containing the
   VHOCs. The boiling point  maximum  of
   100°C  cited in Method 0030 was extended
   to  approximately 135°C  to  include chlo-
   robenzene and ethylene dibromide, com-
   pounds  frequently  determined by the
   VOST  methodology. The  apparatus  shown
   in Figure 1 was used for dynamic spiking
   in the field, with the spiking gas allowed to
   flow  through the  spiking apparatus for 2
   hr  before directing the flow  to the sam-
   pling trains to  minimize any adsorptive
Table 1.   Halogenated Compounds for Which Laboratory Testing has Determined the Applicability of the VOST Method
           Compound
       Boiling point (°C)
                                                                                           Comments
    allyl chloride
    bis(chloromethyl) ether
    carbon tetrachloride
    chlorobenzene
    chloroform
    chloromethyl methyl ether
    chloroprene
    1,3-dichloropropylene
    epichlorohydrin
    ethyl chloride (chloroethane)
    ethylene dichloride (1,2-dibromoethane)
    ethylidene dichloride (1,2-dichloroethane)
    methyl bromide (bromomethane)
    methyl chloride (chloromethane)
    methyl chloroform (1,1,1-trichloroethane)
    methylene chloride
    methyl iodide (iodomethane)
    propylene dichloride (1,2-dichloropropane)
    tetrachloroethylene
    1,1,2-trichloroethane
    trichloroethylene
    vinyl chloride
    vinyl bromide
    vinylidene chloride (1,1-dichloroethylene)
           44-46
           1061
           77
           1321
           60.6-61.5
           55-57
           59.4
           105-1062
           115-1771
           123
           131-1321
           83
           43

           -24.2?
           74-76
           39.8-40
           41-43
           95-96
           1211
           110-1151
           86.9
           -13.43
           164
           30-32
Acceptable performance in laboratory
Decomposes in water; cannot be analyzed
Recovery too high in laboratory study
Acceptable performance in laboratory
Acceptable performance in laboratory
Decomposes in water; cannot be analyzed
Acceptable performance in laboratory
Acceptable performance in laboratory
Decomposes in water; cannot be analyzed
Acceptable performance in laboratory
Acceptable performance in laboratory
Acceptable performance in laboratory
Recovery unacceptably high in laboratory
Erratic and unacceptable in laboratory
Recovery too high in laboratory study
Recovery too high in laboratory study
Acceptable performance in laboratory
Acceptable performance in laboratory
Acceptable performance in laboratory
Acceptable performance in laboratory
Acceptable performance in laboratory
Acceptable performance in laboratory
Acceptable performance in laboratory
Acceptable performance in laboratory
1 Above the maximum VOST boiling point of 100°C; included in the testing because compounds in the range of 100-132°C are frequently tested by the VOST method.
2 Boiling temperature at 730 mm Hg.
3 Below the common lower temperature limit of 30°C usually used for VOST.
4 Boiling temperature at 750 mm Hg.

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           Regulator
     (temperature controlled)
            Certified
            standard
            (spiking
          compounds^
                                                                    Chassis (temperature controlled)
           To train A
                ->• To train B

                Fine metering
                    valves
                (Flow control)
                                                                    1/4" Teflon line
                                                                     (Heat traced
                                                                    and insulated)
                                                                                 111      JL
                                                                              -Q fl Q Q Q D U
                                                                                                      Temperature
                                                                                                         display
                                              Variacs
                                   (To provide temperature control)
                                    Thermocouple selector
Figure 1.  VOSTspiking apparatus.
losses in the sampling  trains. The con-
centration of compounds in the  cylinder
was verified by laboratory GC/MS and GC/
multiple  detector analysis  of a  diluted
sample prepared in a SUMMA®*-polished
canister.
  Analysis of field samples was performed
according to SW-846 Method 5041, ana-
lyzing each tube  individually to establish
distribution  of compounds.  A  total of  6
complete and valid Quad runs (24 Tenax®/
Tenax®-charcoal pairs,  12 spiked, 12
unspiked) is  required to satisfy  the re-
quirements of the field validation protocol.
However, a total of 10 Quad runs was
performed to provide back-up samples in
the event that any  samples became in-
valid due to breakage or loss during analy-
sis. The  2 tubes associated  with each
sample pair were analyzed separately, al-
ways analyzing the Tenax®-charcoal tube
first to minimize the possibility of carryover
from the front tube, where  higher com-
pound concentrations were  expected. All
VOST sampling  tubes were transported
"Mention of trade names or commercial products does
 not constitute endorsement or recommendation for
 use.
and  stored  at  4°C and  were  analyzed
within 30 days after collection.

Results and Discussion
  The complete analytical results for each
sampling train, showing recoveries of dy-
namically-spiked compounds and  of sur-
rogate compounds for the front  and back
tubes individually are shown in  Appendix
A  of  the  project report.  No  corrections
were  performed  for background concen-
trations  because analyte concentrations
in the background samples were less than
five times  the  Method  Detection Limit.
Mean analyte recoveries and precision for
6 sampling runs  are summarized in Table
2.
  The results for the  first and  second
VOST field  evaluation  studies  are com-
pared in Table  3. Using the criteria for
acceptable performance of recovery  be-
tween 50 and 150%, with  precision  (as
expressed by relative standard deviation)
of 50 or less, acceptable  performance of
the VOST methodology for  a  given com-
pound is indicated in Table 3 by an aster-
isk.
  Methyl chloride exhibited  recoveries far
above the  acceptable  range, consistent
with  results obtained in previous studies.
The  common factor in the excessive re-
coveries for methyl chloride appears to be
formation  of the  compound in  the  time
that the halogenated organic compounds
are adsorbed on the sorbent tubes. Method
8240 shows acceptable and  reproducible
performance for methyl chloride, but sor-
bent residence  times  are minimal in this
analytical  methodology. Where sorbent
residence  time  is minimal  (e.g.,  spiked
sorbent tubes are analyzed  immediately),
recoveries are within the reasonable range,
although  somewhat  high.  When  methyl
chloride  and other halogenated  com-
pounds are retained on the sorbent for  a
period  of days,  excessive values for me-
thyl chloride recovery  are observed. Ana-
lytical results for methyl chloride  using the
VOST  methodology are  biased  high,  fre-
quently by a factor of ten or more.
  Analyte  distribution is  summarized in
Table  4.  As  expected,  methyl  chloride,
ethyl chloride, methyl  bromide,  and vinyl
chloride are found almost exclusively on
the back tube, because these compounds
break through Tenax® very readily. How-
ever,  methyl bromide and ethyl chloride

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Table 2.   Summary of Mean Recovery and Precision for 6 VOST Sampling Runs Using Dynamic Spiking
                                Recovery 50-150%—Precision <50% Relative Standard Deviation (RSD)

                         Compound                                                 Average recovery (%)
                                                                  i RSD
propylene dichloride (1,2-dichloropropane)
trichloroethylene
chloroform
methyl chloroform (1,1,1-trichloroethane)
methylene chloride
ethylidene dichloride (1,1-dichloroethane)
chlorobenzene
carbon tetrachloride
1,1,2-trichloroethane
ethylene dibromide (1,2-dibromoethane)
cis-1,3-dichloropropene
vinylidene chloride (1,1-dichloroethylene)
chloroprene
ethylene dichloride (1,2-dichloroethane)
tetrachloroethene
methyl bromide (bromomethane)
trans-1,3-dichloropropene
Acceptable recovery, unacceptable precision
methyl iodide (iodomethane)
Unacceptable recovery (low), acceptable precision
vinyl chloride
allyl chloride (3-chloropropene)
ethyl chloride (chloroethane)
vinyl bromide
Unacceptable recovery (high), unacceptable precision
methyl chloride (chloromethane)
                                               121
                                               119
                                                91.3
                                                91.1
                                                89.9
                                                82.2
                                                81.2
                                                81.2
                                                79.7
                                                79.6
                                                79.5
                                                77.8
                                                72.4
                                                72.3
                                                60.1
                                                54.8
                                                52.3

                                                79.5

                                                41.8
                                                35.6
                                                33.7
                                                29.8

                                               243
                    24.8
                    26.2
                    31.1
                    24.6
                    14.3
                    23.3
                    22.1
                    23.6
                    27.2
                    37.4
                    27.6
                    24.2
                    23.0
                    37.5
                    27.9
                    26.2
                    35.4

                    63.1

                    44.6
                    33.3
                    36.9
                    29.7

                    62.8
frequently show  an approximately even
distribution between the  front tube and
the back tube. Other compounds are dis-
tributed between  the front tube and back
tube, with the highest compound  concen-
tration  on the front tube. Highly haloge-
nated compounds such as methylene chlo-
ride, carbon tetrachloride, and methyl chlo-
roform show a  distribution between front
and back tubes, but with a clear predomi-
nance  on the front tube. Using the crite-
rion of 30% distribution on the back tube
as  an  indicator of breakthrough (Hand-
book:  Quality Assurance/Quality Control
(QA/QC) Procedures for Hazardous Waste
Incineration,  EPA/625/6-89/023, January,
1990),  no breakthrough was observed for
any compound.

Conclusions
  The  following conclusions can be drawn
from the data obtained in VOST field evalu-
ation:
  • The  VOST method performed accept-
    ably for the majority of the candidate
    VHOCs  in  2  field tests.  The VOST
    methodology  showed unacceptable
    performance  for only 2 compounds in
    both field evaluation studies:  methyl
    chloride and allyl chloride.
  • The VOST method performed accept-
    ably for the following compounds in
    only 1 field evaluation:  vinyl chloride,
    ethyl chloride, vinyl bromide, ethylene
    dibromide, and  chloroprene. The suc-
    cess  of  the  methodology for  these
    analytes  is source-dependent.
  • Vinyl  chloride,  allyl  chloride, chloro-
    prene, and vinyl  bromide  all  show
    marginal  or unsuccessful performance
    in the VOST methodology. The pres-
    ence  of the double-bond  in the ana-
    lyte molecule appears to significantly
    decrease the probability of successful
    performance of the VOST method.
  On the basis of  laboratory and field
evaluation studies  for the VHOCs  from
Title III of the CAAA of 1990, the following
recommendations are made:
  • Consideration of the  chemical proper-
    ties of the compounds which were not
    amenable to  the VOST  analytical
    methodology (epichlorohydrin, chloro-
    methyl methyl ether,  bis[chloromethyl]
    ether) predicts that successful perfor-
mance is very unlikely. These com-
pounds are reactive,  polar,  and wa-
ter-soluble. A  method other than the
VOST will be required for  the  suc-
cessful sampling and analysis of these
types of compounds.
Methyl chloride has demonstrated ex-
cessively  high values  for recoveries
in two field evaluation studies, as well
as in laboratory studies. Because of
this  high bias, the VOST is not rec-
ommended as a sampling and  ana-
lytical method  for this compound.
Further study of the VOST should be
performed and/or VOST data should
be collected in order to set appropri-
ate recovery limits for the surrogates
recommended   in the  analytical
method.  At present, the  surrogates
can  only be used qualitatively:   poor
surrogate recoveries  indicate  prob-
lems with the matrix or the methodol-
ogy.
Modification or  replacement of  the
VOST methodology should be inves-
tigated to provide a feasible sampling
and  analytical  method for the volatile,
polar, water-soluble compounds listed
in Title III of the  CAAA of 1990.

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Table 3.   Comparison of Results for First and Second VOST Field Evaluations
              Compound
          First field test'                          Second field test'
Recovery(%)           RSD (%)          Recovery (%)            RSD (%)
methyl chloride
ethylidene dichloride
chlorobenzene
vinyl chloride
vinylidene chloride (1,1-dichloroethylene)
chloroform
propylene dichloride (1 ,2-dichloropropane)
methyl bromide (bromomethane)
ethyl chloride (chloroethane)
methylene chloride
methyl chloroform (1,1,1-trichloroethane)
carbon tetrachloride
ethylene dichloride (1 ,2-dichloroethane)
trichloroethylene
cis-1 ,3-dichloropropene
trans-1 ,3-dichloropropene
1 , 1 ,2-trichloroethane
tetrachloroethene
methyl iodide (iodomethane)
allyl chloride (3-chloropropene)
ethylene dibromide (1 ,2-dibromoethane)
chloroprene
vinyl bromide
937
75.7*
88.2"
110.4'
88.0*
81.8"
67.2*
53.7*
50.3*
77.7*
770*
707*
76.6*
726*
737*
735*
98.0*
97.7*
72.8*
29.9
34.9
40.1
60.7*
53. 8
13.7
22.0
27.3
31.3
14.8
9.6
20.2
28.7
27.1
43.5
47.2
33.0
15.6
26.0
38.1
22.1
21.9
37.6
19.5
31.6
22.4
34.3
243
82.2*
81.2*
41.8
77.8*
91.3*
121*
54.8*
33.7
89.9*
91.1*
81.2*
72.3*
119*
79.5*
52.3*
79.7*
60.1*
79.5
35.6
79.6*
72.4*
29.8
62.8
23.3
22.1
44.6
24.2
24.6
24.8
26.2
36.9
14.3
31.1
23.6
37.5
26.2
27.6
35.4
27.2
27.9
63.1
33.3
37.4
23.0
29.7
Chloromethyl methyl ether, bix(chloromethyl) ether, and epichlorohydrin could not be analyzed by the VOST methodology.
* Acceptable performance by the analyte in the VOST method, using acceptability criteria of 50-150% recovery with percent Relative Standard Deviation (RSD) of 50 or less.
1  Mean of 6 runs (twelve pairs) uncorrected for background.
Table 4.   Distribution Between Front and Back Tubes According to Compound
         Compound
  Average recover (front)
Average recovery (back)
Compounds recovered on the front tube (> 90% on front tube)
cis-1,3-dichloropropene
trans-1,3-dichloropropene
ethylene dichloride (1,2-dibromoethane)
trichloroethene
tetrachloroethene
chlorobenzene
propylene dichloride (1,2-dichloropropane)
chloroprene
1,1,2-trichloroethane
ethylene dichloride (1,1-dichloroethane)
chloroform
allyl chloride (3-chloropropene)
methyl iodide (iodomethane)
ethylene dichloride (1,2-dichloroethane)

Compounds distributed between front and back tubes
methyl chloride (chloromethane)
vinyl chloride
methyl bromide (bromomethane)
chloroethane
vinyl bromide
methylene chloride (chloromethane)
carbon tetrachloride
methyl chloroform (1,1,1-trichloroethane)
          100.0
           99.9
           99.9
           99.7
           99.6
           99.5
           99.5
           99.0
           97.7
           96.8
           95.8
           93.7
           93.2
           92.0
           16.5
           19.3
           36.5
           55.1
           73.2
           81.7
           84.5
           86.3
            0.0
            0.1
            0.1
            0.3
            0.4
            0.5
            0.5
            1.0
            2.3
            3.2
            4.2
            6.3
            6.8
            8.0
           83.5
           80.7
           63.5
           44.9
           26.8
           18.3
           15.5
           13.7

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   James F. McGaughey, Joan T. Bursey, and Raymond G. Merrill are with Radian
     Corporation, Research Triangle Park, NC 27709.
   Merrill D. Jackson is the EPA Project Officer (see below).
   The complete report, entitled "Field Test of a Generic Method for Halogenated
     Hydrocarbons: A VOST Test at a Chemical Manufacturing Facility," (Order No.
     PB95-129144/AS; Cost: $19.50, 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:
           Atmospheric Research and Exposure Assessment Laboratory
           U.S. Environmental Protection Agency
           Research Triangle Park, NC 27711
United States
Environmental Protection Agency
Center for Environmental Research Information
Cincinnati, OH 45268
Official Business
Penalty for Private Use $300
      BULK RATE
POSTAGE & FEES PAID
         EPA
   PERMIT NO. G-35
EPA/600/SR-94/113

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