Document G5YdNMnkpJed3LqmabQ6zJ0ox
EMISSION TEST REPORT NEW REACTOR D-745
CONOCO CHEMICALS COMPANY P.0. BOX 91
ABERDEEN, MISSISSIPPI 39730
APRIL 7, 1982
A
VAB.0001115754
EMISSIONS TEST *
NEW REACTOR D-745 CONOCO CHEMICALS COMPANY
ABERDEEN. MISSISSIPPI
I. INTRODUCTION
A. Source Information B. Testing Personnel C. Process Description
II. SAMPLING RESULTS SUMMARY
A. Emissions Test Results B. FVC Production During Tests
III, SAMPLING PROCEDURES
A. Sampling Apparatus B. Sampling Procedures
IV. ANALYTICAL PROCEDURES
A. Analytical' Apparatus 1. Slurry Samples 2. Reactor Opening Loss Samples 3. Reagent s
B. Analytical Procedures 1. Slurry Samples 2. Reactor Opening Loss Samples
V. CHAIN OF CUSTODY
VI. APPENDIX
Operating Data Sheets Sampling Data Sheets Analytical Calculations Analytical Data Standard Gas Certifications Reactor Opening Loss Calculations
A
VAB.0001115755
EMISSIONS TEST NEW REACTOR D-745 CONOCO CHEMICALS COMPANY ABERDEEN, MISSISSIPPI
I. INTRODUCTION
In accordance with 40 CFR 61, Section 61.67, an emissions test was conducted on March 9 and 10, 1982 for the newly constructed PVC polymerization reactor D-745. The purpose of the test was to demonstrate compliance with 40 CFR 61, Sections 61.64 (a) (2) and 61.64 (e) (1) (ii).
A. * Source Information
The emissions test was conducted at:
Conoco Chemicals Company Highway 25 Aberdeen, Mississippi 39730
Questions concerning the testing or this report should be directed to:
R. A. Frohreich, Chief Process Engineer Telephone Number (601) 369-8111, extension 2239
Dave Mahler, Environmental Engineer Telehone Number (601) 369-8111, extension 2285
B. Testing Personnel
The testing and analytical work was conducted by Conoco Chemicals Company personnel at the Aberdeen facility. Mr. Jerry Banks of the Mississippi Department of Natural Resources, Bureau of Pollution Control observed testing on March 10, 1982. Personnel involved in sampling and sample analysis were:
Dan Cash - Engineering Co-Op Student Dave Cox - Manufacturing Chemist Jimmy Grace - Quality Control Technician Dave Mahler - Environmental Engineer Veldon Messick - Senior Process Engineer
C. Process Description
Vinyl chloride monomer is received at the plant site in railroad tank cars and is transferred by compressors to the VCM storage sphere. The VCM is then pumped to fresh VCM batch tanks which are located in each of the two reactor areas.
VAB.0001115756
MISSIONS TEST NEW REACTOR D-745 CONOCO CHEMICALS COMPANY ABERDEEN, MISSISSIPPI
A
I. INTRODUCTION (CONTINUED)
C. Process Description (Continued)
PVC is produced batchwise from the vinyl chloride monomer. The plant produces only one type of resin; that by the suspension polymerization process. The reactor is first . evacuated to remove air and inert gases and is then charged with carefully measured quantities of VCM, water and a suspension agent. The reaction is initiated with a peroxidetype catalyst. Following completion of polymerization, the reaction is killed and the unreacted VCM is removed from the reactor in the recovery sequence.
The recovery system is designed to recover unreacted VCM for recycle to subsequent batches. During the pressure recovery phase, VCM vapors are pulled from the reactor and compressed, condensed and liquified. The liquified VCM is routed to the recovered monomer tanks. As a part of the recovery operation, steam is injected into the slurry to aid in the removal of residual VCM in the slurry. When the reactor pressure approaches atmospheric pressure, vacuum pumps are started and the reactor pressure is reduced to a vacuum. These VCM vapors are also compressed and liquified and the liquified VCM is routed to the recovered monomer tanks. By this time the slurry has been brought to a boiling condition by action of the steam injection and the vacuum. The steam blows through the slurry and purges the vapor space above the slurry before being pulled out of the reactor by the recovery system. Cooling water is then put on the reactor in order to cool the slurry down prior to dumping the reactor.
When the recovery step is complete, the PVC/water slurry is dumped through a slurry screen which removes oversize material. The slurry is then pumped to blend tanks. After product pumpout, the reactor is rinsed to the blend tanks, which completes the reaction batch cycle.
The PVC/water slurry is pumped from the blend tanks to a centrifuge in the drying area, and the extracted water is discharged to the process sewer. Wet cake is fed to a dryer in which- the resin is dried. The dried resin flows through a product sifter where oversize material is again separated and collected. Resin is then pneumatically conveyed to storage silos and eventually shipped from the plant in trucks or hopper cars.
VAB.0001115757
*
t
EMISSIONS TEST NEW REACTOR D-745 CONOCO CHEMICALS COMPANY ABERDEEN, MISSISSIPPI
II. SAMPLING RESULTS SUMMARY
A. Emissions Test Results
The following is a summary of results from sampling and analyzing the reactor D-745 vapor space and dumped slurry for each of three reactor batches.
D-745 Batch No.
D-745-155 D-745-156 D-745-157
Date
3/9/82 3/10/82 3/10/82
Resin Grade
5265 5385 5385
Vinyl Chloride Emissions
(Lbs. VCM/MM Lbs. PVC)
Slurry
Total
65 88 153 43 67 110 210 136 346
The process employed at this plant utilizes the reactor for poly merization and stripping. Because VCM flashes out of the slurry and into the vapor space while the reactor is being dumped, it is impossible to accurately segregate the slurry residual and the reactor opening loss. The standard specifies maximum emissions of 400 lbs. VCM/MM lbs. PVC from the slurry and 20 lbs. VCM/MM lbs. PVC from the reactor vapor space. Thus, a maximum emission of 420 lbs. VCM/MM lbs. PVC from the entire reactor is applicable to reactor D-745.
The results of the emission tests summarized above demonstrate that reactor D-745 was in compliance with Sections 61.64 (a) (2) and 61.64 (e) (1) (ii) for each of the three reactor batches tested. The .total emissions from reactor D-745 did not exceed 420 lbs. VCM/MM lbs. PVC produced.
B. PVC Production During Tests .
The Aberdeen plant had a nominal PVC production capacity of 400 MM lbs. PVC/year at the time of the D--745 emission test. This corresponds to a daily average of 1,096 M lbs. PVC/day. During the two days of emission testing, the plant produced 971 M lbs. PVC/day, which is less than the nominal plant capacity. The maximum production rate can only be achieved in the-winter time when colder cooling water temperatures are available which allow for higher catalyst loadings. Futhermore, the maximum production rate requires perfect reactor scheduling without any reactor or dryer downtime due to maintenance or other delays.
VAB.0001115758
EMISSIONS TEST NEW REACTOR D-745 CONOCO CHEMICALS COMPANY ABERDEEN, MISSISSIPPI
II. SAMPLING RESULTS SUMMARY (CONTINUED)
B. PVC Production During Tests (Continued)
Since the plant utilizes a batch polymerization process, the plant*s production rate is increased or decreased by processing more or less reactor batches per unit time. The size of the reactor batches is varied only slightly over long periods of time for any specific grade of resin produced. During the emission testing, reactor D-745 was charged with quantities of VCM which are representative of the current batch size for reactor D-745.
A
VAB.0001115759
EMISSIONS TEST NEW REACTOR D-745 CONOCO CHEMICALS COMPANY ABERDEEN, MISSISSIPPI
III. SAMPLING PROCEDURES
A. Sampling Apparatus
Reactor opening loss samples were taken with the apparatus shown on Figure 1. The components of the apparatus are described as follows:
*
1. New, unused teflon tubing;
6.4 mm OD.
2. Stainless steel plug valves with teflon plugs, stainless steel hose connectors and interconnecting tubing.
i
3. 15 liter Calibrated Instruments multilayer gas bags.
4. Rigid container, sealed airtight with RTV gel sealant.
5. Gast vacuum pump.
6. Calibrated MSA sampling pump rotameter.
7. Needle valve
8. V Tygon tubing.
B. Sampling Procedures
The reactor slurry samples were obtained from a sample tap on the reactor dump line. Prior to taking the samples, the sample line was purged for approximately 10 seconds with slurry. The three slurry samples were grabbed 5, 8, and 11 minutes into the dump period. 2-ounce sample bottles with screwed on covers were used to collect the samples. Immediately following sampling, the sample bottles were taped shut with electrical tape and labeled with the date, time and reactor batch number. The samples were then stored under refrigeration and analyzed within 24 hours of collection.
Reactor vapor space samples were taken immediately after the slurry dump land rinse. The sampling train was tightly assembled, using a sample bagtwhich had been leak checked overnight. The sample bag was evacuated until the rotameter indicated zero flow, and the valve was shut. Reactor D-745Ts top manway was then opened, and the sampling line was lowered into the top of the reactor. The sampling line was purged at a rate of 1 to 2 liters per minute for approximately 1 minute. Immediately following this purge, the sample was taken. The top of the reactor, the middle of the reactor and the bottom of the reactor (within 6 inches of the bottom) were each sampled for 5 minutes, in that order. Flow
VAB.0001115760
EMISSIONS TEST NEW REACTOR D-745 CONOCO CHEMICALS COMPANY ABERDEEN, MISSISSIPPI
III. SAMPLING PROCEDURES
A. Samp1in
aratus (Continued)
through the sampling train was maintained at 0.5 liters per minute throughout the sampling period. At the end of sampling, the valve above the sample bag was shut, the pump turned off and the sampling apparatus disassembled. The sample bag was trans ferred to the plant*s laboratory and analyzed within 24 hours of sample collection.
VAB.0001115761
1a
FIGURE 1 REACTOR OPENING LOSS SAMPLING APPARATUS
A
Tygon
Vacuum Pump.
VAB.0001115762
EMISSIONS TEST NEW REACTOR D-745 CONOCO CHEMICALS COMPANY ABERDEEN. MISSISSIPPI
IV. ANALYTICAL PROCEDURES
A. Analytical Apparatus
1. Slurry Samples
The following apparatus was used to analyze slurry samples for residual VCM:
a) Vials, unused with Septa and aluminum seals. b) Analytical balance, with minimum sensitivity of
0.001 gram. c) Syringe, 100 *il, Hamilton #710. d) Vial Sealer, P-E No. 105-0106 e) Filter Flask, 250 ml capacity. f) Buchner funnel, 7 cm. g) Filter paper, Whatman No. 4 h) , disposable aluminum i) Cork borer j) Oven, Blue-M natural draft k) Gas chromatograph, P-E F-42 Headspace Analyzer 1) Chromatographic column, stainless steel 2 m X 3.2 mm,
containing 0.4% Carbowax 1500 on Carbopak C. m) Thermometer, minimum range 0-100C, minimum sensitivity
0.1 C. n) Sample Tray Thermostat System, Haake Model N3B. o) Integrating Computer, Spectra Physics, SP 4000. P) Barometer, sensitivity 0.1 mm Hg.
q) Thermometer, accurate to 1C, near GC.
r) Recorder, Houston Instruments potentiometric strip chart recorder set on 1 mm full-scale response and 1 cm per minute chart speed.
2 Reactor Opening Loss Samples
The following apparatus was used to analyze gas bags for VCM:
a) Gas chromatograph, HP model 5711 A with a 1.0 ml heated sampling loop in a manual sample valve and flame ionization detector.
b) Recorder, Perkin Elmer potentiometric strip- chart recorder set on 1 mv full-scale response and 1 cm per minute chart speed.
A
VAB.0001115763
EMISSIONS TEST NEW REACTOR D-745 CONOCO CHEMICALS COMPANY ABERDEEN, MISSISSIPPI
IV. ANALYTICAL PROCEDURES (CONTINUED)
A. Analytical Apparatus (Continued)
2 Reactor Opening Loss Samples (Continued)
c) Chromatographic column, stainless steel, 2.0 m X 3.2 mm, containing 80/100 mesh chromosorb 102.
d) Flow meter, rotameter type with 0-200 ml/minute capacity, with control valve.
e) 6 gas regulators, dual stage brass. f) Thermometer, mercury type, accurate to 1 C, mounted near
the sample loop. g) Barometer, accurate to 0.1 mm Hg. h) Pump, ITT diaphram. i) Tubing, teflon, 6.4 mm O.D. j) Sample bags, Calibrated Instruments multilayer
bag of aluminized Mylar. k) Data Processor, Spectra Physics SP4000.
3. Reagents
The following reagents were used to analyze slurry samples and gas bags for VCM:
a) b) c) d) e) f)
Nitrogen Gas, zero grade. Hydrogen Gas, zero grade. Compressed Air, zero grade. Calibration Gas, 496 ppm VCM in nitrogen, certified. Calibration Gas, 2188 ppm VCM in nitrogen, certified. Calibration Gas, 4015 ppm VCM in nitrogen, certified.
B. Analytical Procedures
1. Slurry Samples
The following procedure was used to analyze slurry residual VCM:
a) Sample Storage
+
Slurry samples must be stored under refrigeration. Analyses will be performed after sample has cooled to at least 30 C and within 24 hours of collection.
VAB.0001115764
It
I
EMISSIONS TEST NEW REACTOR D-745 CONOCO CHEMICALS COMPANY ABERDEEN. MISSISSIPPI
A
IV. ANALYTICAL PROCEDURES (CONTINUED)
B. Analytical Procedures (Continued)
1'. Slurry Samples (Continued)
b) Slurry Samples
%
Tareavial with septum and seal and record weight. Tare and record the weight of an aluminum pan (label pan). Set up vacuum aspirator and filter flask assembly. Pour slurry into funnel and start vacuum until steady stream of water stops (15 sec.). Remove vacuum. Use the cork borer transfer about 1.5 g. to the vial and seal it. Take another plug for solids and transfer to an aluminum pan. Quickly weigh and record the pan and save this sample for determination of total solids. Weigh and record the vial weight.
c) Preparation of Gas Chromatograph
Flame should be lit at least one hour prior to analyses. Nitrogen pressure of 1.4 kg/cm gives 32 cc/minute. Set hydrogen at 2.1 bar and air at 2.8 bar. The oven should be set at 65 C, the neddle at 150 C, and the injector and detector at 150C.
d) Programming the -Chromatogrpah
Set "1" at 3 seconds, "A" at 07, "BF" at 09 and "S" at 2 minutes. Set ''Analysis + Backflush Times" toggle switch at "X0.1" position. Both range and attenuation should be at a value of "1".
e) Preparation of Sample Turntable
The bath should have been on at least 4 hours prior to use. Check the temperature in the turntable to insure it is at 90+0.5 C. Insert vials in turntable as follows: Positions 1 and 2 are old standards in the vials from a previous run; positions 3-6 are the calibration standards; positions 7-30 may be samples of any type.- Condition all samples including standards at least one hour (not to exceed five hours).before analyzing.
After conditioning, start the chromatograph program and recorder.
VAB.0001115765
EMISSIONS TEST NEW REACTOR D-745 CONOCO CHEMICALS COMPANY ABERDEEN, MISSISSIPPI
ANALYTICAL PROCEDURES (CONTINUED)
B. Analytical Procedures (Continued)
1. Slurry Samples (Continued)
A
f) Determination of Total Solids
Place the label aluminum pans in the oven. The oven should be at 110+5 C. Allow the samples to dry for 45 minutes. Remove and cool to room temperatures. Record the weight and calculate the fraction of total solids (dry weight divided by wet weight). Record this value on the data sheet.
g) Calibration Standards
Calibration standards are prepared by filling the vials (at least two sets per series of samples) with the vinyl chloride/nitrogen standards, rapidly seating the septum and sealing with the aluminum seal. Use only stainless steel lines from the cylinder to the vial. The sample line from the cylinder must be purged into the hood prior to filling vials. After line purging, place the end of the tubing into the vial near the bottom and allow purging of the vial for one minute at 1000 cc/minute. (Hold the vial with finger tips only to minimize temperature affect of hand). Slowly remove tubing and quickly cap the vial with the septum and seal. Inject 100 ul of deionized water into vial.
2. Reactor Opening Loss Samples
The following procedure was used to anlayze reactor opening loss samples for VCM:
a) Sample Storage
*
Samples must be kept out of direct sunlight during storage. Analysis will be performed after the bag has equilibrated to laboratory temperature and within 24 hours of sample collection.
b) Sample Recovery
Connect the sample bag to the GC sample valve inlet
direct with Teflon ferrules. Prepare the equipment such
that the sample gas- will pass through the bag, through
the sample loop, through the pump, rotameter, and flow
control valve at a rate of 100 ml/minute.
VAB.0001115766
EMISSIONS TEST NEW REACTOR D-745 CONOCO CHEMICALS COMPANY ABERDEEN, MISSISSIPPI
h
ANALYTICAL PROCEDURES (CONTINUED)
B. Analytical Procedures (Continued)
2 Reactor Opening Loss Samples (Continued)
c) Analysis
The GC column
should be oven and
previously sample loop
prepared such that are equilibrated
atthe130oWC
and 100 respectively. The hydrogen flame should be ignited
< at least one hour prior to analysis using constant and
previously optimized flow rates for both hydrogen and air.
Carrier flow at 30 ml/minute should also be established at
least one hour prior to analysis. (Leave instrument on
overnight during routine use.) Observe the baseline to
determine both noise level and drift at the 1 x 10^ sen
sitivity are acceptable.
*
With the recorder on and an attenuator setting of 1 x 10 2 ,
purge the sample loop with the sample gas at least 30 seconds
at 100 ml/minute. Stop the pump, and when the rotameter just
indicates no flow, activate the sample valve to inject the
sample gas. Mark the injection point on the chart and read
the loop temperature and laboratory pressure and temperature.
Record all conditions on the chart. Start the SP4000.
With the laboratory pressure and temperature, determine the water content of the sample at analysis from a water saturation vapor pressure table (assume 100% relative humidity in the sample).
d) Instrument Calibration
Fill evacuated Calibrated Instruments bags with the standard gases, always using the sample bag for the same concentration, daily. Use only stainless steel or the appropriate Teflon tubing connectors. Allow bags to equilibrate to laboratory temperature.
m
fcr
Measure each standard gas in duplicate each day using the same GC conditions and procedures described in the above analysis section. Record all conditions as described earlier for each analysis.
VAB.0001115767
EMISSIONS TEST NEW REACTOR D-745 CONOCO CHEMICALS COMPANY ABERDEEN, MISSISSIPPI
A
V. CHAIN OF CUSTODY
Slurry samples and gas bags were handled as follows:
Slurry Samples
Sample Run No.
1
2
3
Taken By
Dave Mahler Dan Cash Dave Mahler
Transported By
Dave Mahler Veldon Messick Dan Cash
Analyzed By
Jimmy Grace Dave Cox Jimmy Grace
Reactor Opening Loss Gas Bags
Sample Run No,
Taken By
1' 2 3
Dave Mahler Dave Mahler Dave Mahler
Transported By
Veldon Messick Dan Cash Dan Cash
Analyzed By
Dave Cox Dave Cox Dave Cox
VAB.0001115768
EMISSIONS TEST NEW REACTOR D-745 CONOCO CHEMICALS COMPANY ABERDEEN. MISSISSIPPI
VI. APPENDIX
The Appendix of this report contains the raw data and calculations used to obtain the sampling results. This information is pre sented In the following order:
*
Operating data sheets for reactor D-745 during the three-batch sampling period.
Sampling data sheets.
Reactor Opening Loss and Slurry Residual Analytical Calculations.
Integrator and GC printout data.
Standard Gas Certifications.
Reactor Opening Loss Calculations
A
VAB.0001115769
REACTOR .
Water Tk.
FORMULA
I
Colloid
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VC Tank
LLjCatalyst
TYPE
tints
Inches Counts
M
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Type
4-
'DATE
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Counts RVCM
02'Lcvel
-PH Pressure Seal Water Seal Water Press
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Pre-charge Amps
lv
Running Temp.
A rPVA IN.
Pressure
pa
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Actual
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Charge Start
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Charge Complete Catalyst Start
Time Reaction Temperature Reached
Actual
Dev
Standard 3 Minutes
Catalyst Complete
Turn Around Time
Recovery Start Run Time
Ilrs.
*
Recovery Complete Amt. Recovered To
Mi
Actual
Dev
Standard 68 Minutes
Actual
+ *
Dump Start To Tank
Bldg. No.
Standard 25 Minutes
mments:
Dump Stop Chcm Wash Start Chem Wash Finish Rinse Start Rinse Complete Swirl Start Swirl Complete
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Steam
Time Reaction Killed
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VAB.0001115771
ilEACTOR
FORMULA
TYPE
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Water
CoIIoid^Mi^LGa]
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Counts
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OH* Level OH Pressure Seal Water
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REACTOR
FORMULA
TYPE
DATE
/& ~
J3URA SEAL
ColloidHal
VC Tank
%
-Catalyst - Cal
Pre-charge Amps
unts
.Inches. Counts FVCM.
Type
A
Counts RVCM
OR* Level -t)R Pressure Seal Water Seal Water Press rPVA IN
Inches GPM
t M~RG, -/Jc y'
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F Pressure
pa
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SH>
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ie Prcsscl
Evacuation Start
10 Minutes
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nchesH
Actual
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Charge Start
^Standard 11 Minutes
Charge Complete Catalyst Start
Time Reaction Temperature Reached
Catalyst Complete
Turn Around Time
His.^2
Recoveiy Start Run Time 6L
Recovery Complete Amt. Recovered To
Mi
H
Actual
Dev
Standard 3 Minutes
Actual
Dev
Standard ^BMSnutcs
Actual /JDtv3z>I7
Dump Start To Tank
Bldg. Noj
Standard 25 Minutes
Dump Stop Chem Wash Start Chem Wash Finish Rinse Start Rinse Complete Swirl Start
Swirl Complete
Total Stripping
Steam
Time Reaction Killed
Actual
Dev
Standard 25 Minutes
Actual
Dev
Standard 10 Minutes
Actual
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-1 * .
*'1,:+ > - ' ' j _ * :d ^ . `," .
1
*- + *
. - ._. H
i ! I S*--. .. L
l' I
*. **
L
L
L
r
,-
** >- 4 .r ,
. -^r ' -T* 1 ; ^ r. -
- -r
f . 'V * - -
'
.*-. /** ,
'- *r>
` p*J^_ . Cb
v "-
'
*
" "
*-
^ . -
*-
*.
J 1 "-* ,a */ ! ^
j
I * -
> T * -*
-
*r
v ' - +*'
i* . v-
* a. #
/*->'.' -a.**- -vr; ? "-.V
m -- ^*
>1
'r---"!, %*
1 ' 4
Ip"*
`
K#
- - / *. *
*.* r '
^ * '/ ^ #
r r*
^ V>
.
_ +- -
* - A ** .
*'_*.' , l P . . J . m* *. +r
- *.* '*
A
MlKNTlAL
r r
i r f i
^ s ^ . * '
* b> * ' ,
l.'ur
' '
. - `' 1
/ '.''
' j
-
t :`7V*.
i
-*r. T-'. :#:.
i f -: ""w f*;.r'. i i i
{
i i i
j
i i i
:-:.->'T--
P V.
-.' ^ *-
.+
t, . ' l'
" . v t '' r
.k ',
_f .
I'
L
I
[
;;
c*j-<` ** frv* * /i.y,-*c-' > -V -1-' '; r
l^^ii t -* 3? *
.r y- . ^
p ; * - *
m
*
rr 4 -
. r
h
^.
*
J 1* , 1 *
l t ,x L
* -\
*
i*
* *.
v' ,
^
J
,..:; ,--.,.,:
L - ,r ^ t w ?*-
*
*
4
^ a ,4
L.
r^"
*4
A. V-
? ^ --r>rC j-
*i
^*
*
t<
*4 >
i^
fc
kf *
A
REACTOR D-7U5 COMPLIANCE TEST
3DATE ,
=
BLEND NO.:
RESIN:
2.
SLURRY SAMPLES DUMP STARTED:
7: MM
Sample
/
3
Time
Taken By
7' 27frH
7,'
^6 t>ib
Transported By
Analyzed By
Wt MH**-
C<ra<rc.
trn#*- jv*y
iyud'Uffltex- <r/***f 6r*"-
REACTOR OPENING LOSS
Time Started
Taken By
Transported By
OfH'b MttHU/C
1/hiVCH
Analyzed By
VAB.0001115776
REACTOR D-7U5 COMPLIANCE TEST
DATE : $
BLEND NO.:
u
<3 V3ffX.
RESIN:
SLURRY SAMPLES DUMP STARTED:
33 ??rA
Sample
/
Time
Taken By
2 f cf % pM P fatf
^
2r 4^?^
Transported By
s/glbOfil
I/&m tfgSSttK.
Analyzed By
0QVC Cof
DvC Cf
REACTOR OPENING LOSS
Time Started
pa
Taken By
pft\/- mmjML.
DAf>r C/H. &
Transported By
p c/te ^
Analyzed By
(kce. ^0/
` VAB.0001115777
REACTOR B-7^5 COMPLIANCE TEST
Z/lDATE:
C
BLEND NO.:
RESIN: 5"35
SLURRY SAMPLES DUMP STARTED:
Sample /
Time
z //'
l('(f 3
Taken By Ot-t7 pen
ferl
Transported By C D
0C
Analyzed By
GraO^
P
a.
REACTOR OPENING LOSS
Time Started //:3S-
Taken By ' /fc/y
*
Transported-By - *
1
VAB.OOOl115778
PPM, VCM IN AIR BAG
*
SAMPLE ID: ~?X>VS SleAjJ u 5^37? f
DATE:
3Z/o/
s , %/ OjOJt^KV
Sample Loop Temperature for Standard (Tr)
Sample Loop Temperature for Sample (Ts)
Barometric Pressure for Standard (Pr)
Barometric Pressure for Sample (Ps)
%
Water Vapor Content of Bag (B)
Response Factor (Rf) * Area Standard PPM, VCM in Standard
Area of Sample (As)
C vcm As X PR X Ts X 1 RF Ps Tr
/OO
/OP
7
12
llonolr
Bag Temperature (B)
VAB.0001115779
M
CONFIDENTIAL'4
ANALYSIS OF PVC SLURRY AND WET CAKE FOR PPM. VCM
SAMPLE TYPE:
DATE:
>b- g~Z-
P-EACTOR: ~74 $
LOT #:
^</-^7g-
Response Factor (RF)
Area of Sample (As) Whole Sample Weight (SW) Dry Weight -J- wet weight (TS)
SW x TS *= Resin Weight (RW)
RW -J- 1.4 - Resin Volume (RV) SW - RW = Water Weight (WW) RV + WW = Sample Volume (SV) 23.0 - SV * Vial Volume (W) Lab Barometric Pressure at the Time
the Standards were Prepared (P) Lab Temperature at Time Standards were
Prepared in K * C + 273 = (T) 1 - TS * Water Fraction (TW)
/9a, s
. 'M J.
.7*7 . H9S -1 -a-S A at .7/ft
RVCM (dry)
VV x 10 -3 RW
+ (tS x 2.36 x 10-3)
RVCM of Sample Dry Basis
li.Tl
\hi
VAB.0001115780
1
CONFIDENTIAL IB
ANALYSIS OF PVC SLURRY AND WET CAKE FOR PPM.L VCM
SAMPLE TYPE:
S3 -5__________
DATE: _______ 3 -SO
__________
REACTOR:
?4S
LOT #:
J* > g"
Response Factor (RF) Area of Sample (As) Whole Sample Weight (SW)
Dry Weight -f- wet weight (TS) SW x TS " Resin Weight (RW) RW -J- 1.4 Resin Volume (RV) SW - RW = Water Weight (WW) RV + WW = Sample Volume (SV) 23.0 - SV Vial Volume (W) Lab Barometric Pressure at the Time
the Standards were Prepared (P) Lab Temperature at Time Standards were
Prepared in K = C 4- 273 (T) 1 - TS - Water Fraction (TW)
RVCM (dry)
W x 10 -3 + ITS x 2.36 x 10-3) RW
RVCM of Sample Dry Basis
2V S
'.M*V
/3g, s
<5 S5 2
I 4U=i .3 IS
_______i uu
S v1
3i. 7 ?
_____>_3_Z_
h
As P
STt
VAB.0001115781
ANALYSIS OF PVC SLURRY AND WET CAKE FOR PPM, VCM
SAMPLE TYPE: DATE:
S'Z.LS_________
_______________
*
F.EACTOR: LOT #:
75
3 <-) I'Vfj
Response Factor (RF)
Area of Sample (As) Whole Sample Weight (SW) Dry Weight -J- wet weight (TS) SW x TS * Resin Weight (RW) RW 1.4 = Resin Volume (RV) SW - RW Water Weight (WW) RV + WW - Sample Volume (SV) 23.0 - SV = Vial Volume (W) Lab Barometric Pressure at the Time
the Standards were Prepared (P) Lab Temperature at Time Standards were
Prepared in K = C + 273 = (T) 1 - TS = Water Fraction (TW)
RVCM (dry)
W X 10-'3^ + (TS X 2.36 X 10-3)
ml
RVCM of Sample Dry Basis
As P
VAB.0001115782
I
PPM, VCM IN AIR BAG
A
Sample Loop Temperature for Standard (Tr) Sample Loop Temperature for Sample (Ts) Barometric Pressure for Standard (Pr) Barometric Pressure for Sample (Ps)
*
Water Vapor Content of Bag (B) Response Factor (Rf) - Area Standard
PPM, VCM in Standard Area of Sample (As) C vcm = As X PR X Ts X 1
SF Ps Tr I^B
Bag Temperature (B)
/do
76 ^ a ^ 3
4*2,3
VAB.0001115783
ANALYSIS OF PVC SLURRY AND WET CAKE FOR PPM. VCM
SAMPLE TYPE:
DATE:
3 to- a
REACTOR:
7S
LOT #:
3g3gl
Response Factor (RF)
Area of Sample (As)
Whole Sample Weight (SW)
Dry Weight -J- wet weight (TS)
SW x TS = Resin Weight (RW)
RW -- 1.4 ~ Resin Volume (RV) SW - RW - Water Weight (WW)
RV + WW - Sample Volume (SV)
23.0 - SV = Vial Volume (W)
Lab Barometric Pressure at the Time the Standards were Prepared (P)
J
Lab Temperature at Time Standards were Prepared in K * C + 273 * (T)
1 - TS = Water Fraction (TW)
RVCM (dry)
VV x 10 -3 RW
+ (tS x 2.36 x 10`3)
RVCM of Sample Dry Basis
3tm 2 2,))
15 lJlL
TW x 1.82 x 10-3
As P
EFT
VAB.0001115784
I
-d
ANALYSIS OF PVC SLURRY AND WET CAKE FOR PPM. VCM
SAMPLE TYPE:
S.5.
DATE: _____l-/0-XT_
REACTOR:
7V S
LOT #:
4 38"L-
Response Factor (RF) Area of Sample (As)
n
Whole Sample Weight (SW)
Dry Weight -J- wet weight (TS)
SW x TS - Resin Weight (RW)
RW -- 1.4 * Resin Volume (RV)
SW - RW - Water Weight (WW)
RV + WW = Sample Volume (SV)
23.0 - SV * Vial Volume (W)
Lab Barometric Pressure at the Time the Standards were Prepared (P)
Lab Temperature at Time Standards were Prepared in K * C + 273 (T)
1 - TS = Water Fraction (TW)
/*<=! 7 a U?
_Lj>32____
. 7g
h bu If
RVCM = (dry)
VV x 10 -3 RW
+ (tS x 2.36 x 10-3) +
RVCM of Sample Dry Basis =
TW x 1.82 x 10
94,o
*i. *~7
.5r
.c?xl
As P
R3TT
VAB.0001115785
S CL
ANALYSIS
....................................................................................................................................
"
OF PVC 1 --"M
SLURRY AND WET
---
'
--
M
CAKE FOR PPM.
-
-M
-
II
!
!
f
VCM
SAMPLE TYPE:
S1ZS
DATE:
3-/0- R-a-
REACTOR: ~7 </ S LOT #: 3M3 8X
Response Factor (RF)
Area of Sample (As) Whole Sample Weight (SW) Dry Weight -f- wet weight (TS) SW x TS - Resin Weight (RW) RW 1.4 Resin Volume (RV) SW - RW * Water Weight (WW) RV + WW = Sample Volume (SV) 23.0 - SV - Vial Volume (W)
Lab Barometric Pressure at the Time the Standards were Prepared (P)
Lab Temperature at Time Standards were Prepared in K - C + 273 * (T)
1 - TS = Water Fraction (TW)
9 Of Soy
jrtoy
't*5 L|hg___ >7?; >S?L
/ 5sr7
PI % UI 3
73
a qs
*3 S
RVCM = /VV x 10 (dry) \~~RW-----
x 2.36 x 10
RVCM of Sample Dry Basis *
As P RF"T
VAB.0001115786
zp# ROL- ^
PPM, VCM IN AIR BAG
d
a
SAMPLE ID: ? *f 3g&
S3&S Ja.~->. ? H S
DATE: 3^Jb- Pi______________________
Sample Loop Temperature for Standard (Tr)
-*-
Sample Loop Temperature for Sample (Ts)
Barometric Pressure for Standard (Pr)
Barometric Pressure for Sample (Ps)
%
Water Vapor Content of Bag (B)
Response Factor (Rf) Area Standard PPM, VCM h" Standard
Area of Sample (As)
C vcm * As X PR X Ts X 1
RF Ps Tr
T^B
Bag Temperature (B)
T>$7
A
VAB.0001115787
*
ANALYSIS OF PVC SLURRY AND VIET CAKE FOR PPM. VCM
SAMPLE TYPE:
S3 S^
DATE: ?--/P-- AT-
'RiS-ll-gX
Response Factor (RF)
Area of Sample (As)
Whole Sample Weight (SW)
Dry Weight -f- wet weight (TS) SW x TS Resin Weight (RW)
RVJ 1.4 = Resin Volume (RV) SW - RW * Water Weight (WW) RV + WW = Sample Volume (SV)
23.0 - SV - Vial Volume (W)
X
Lab Barometric Pressure at the Time the Standards were Prepared (P)
Lab Temperature at Time Standards were Prepared in K = C + 273 (T)
1 - TS * Water Fraction (TW)
RVCM (dry)
VV x 10 -3 RW
+ (TS x 2.36 x 10 -3
RVCM of Sample Dry Basis
+ (TW x 1.82 x 10
140
*
As P ITT
VAB.0001115788
CONFIDENTIAL
ANALYSIS OF PVC SLURRY AND WET CAKE FOR PPM. VCM
SAMPLE TYPE:
DATE:
S- >0- gx
'Rfirro 3-n-Zi-
REACTOR: LOT #:
?5
Response Factor (RF)
V
Area of Sample (As)
Whole Sample Weight (SW)
Dry Weight --wet weight (TS)
SW x TS 3 Resin Weight (RW)
RW -J- 1.4 * Resin Volume (RV)
SW - RW * Water Weight (WW)
RV + WW = Sample Volume (SV)
23.0 - SV 33 Vial Volume (W)
Lab Barometric Pressure at the Time the Standards were Prepared (P)
Lab Temperature at Time Standards were Prepared in K 38 C + 273 = (T)
1 - TS * Water Fraction (TW)
*
=
-
" -
-
=
/S*7'*f
O.3KT fgS
.C 1 .SQ7 .`SfcX
.uiz
23^ 7&Q
.3g
RVCM (dry)
/VV x 10"3\ + (TS x 2.36 x 10"3) + (TW x 1.82 x 10
\ RW
)
RVCM of Sample Dry Basis
M4. \. *v.
As P
EFT
VAB.0001115789
1
A
ANALYSIS OF PVC SLURRY AND WET CAKE FOR PPM. VCM
SAMPLE TYPE
DATE : 3-IQ- ff"2-
REACTOR:
LOT f:
7? 5
Response Factor (RF)
Area of Sample (As) Whole Sample Weight (SW) Dry Weight -J- wet weight (TS) SW x TS * Resin Weight (RW) RW -J- 1.4 Resin Volume (RV) SW - RW - Water Weight (WW) RV + WW = Sample Volume (SV) 23.0 - SV * Vial Volume (W) Lab Barometric Pressure at the Time
the Standards were Prepared (P)
Lab Temperature at Time Standards were Prepared in K = C + 273 (T)
1 - TS * Water Fraction (TW)
a ii 0.81S
, 53 xM
t ip
RVCM (dry)
VV x 10 -3 RW
+ ITS x 2.36 x 10-3) + (tw x 1.82 x 10
RVCM of Sample Dry Basis
/3X
W.i
, e> V
%
As F
VAB.0001115790
1 kJ
6
i
TOTRLS
291 264 X1 m ^w1JL7I
*** * w *-* .*
1 Oi *^r
117
4556 1814
T1 OC
wl X --* --*
O *. 7i OiC xO.
F L V
v
OCiTjc
2936
OQ-TC
X.
RUCM
1982 MRR 18 14=23=33
CHRHNEL 2
RUN 46
FILE 2
METHOD 5
X HDEX S.RMT=
1*
\
1
SRMPLE
*
588
XF=
1
NOME
CQNC
RT RRER
KF
1
UCM 4
. 173 - 565 38.32 2. 418
48 58 72 182
589 1660 89828 7102
F F L
2936 2936* 2936 2936
TOTRLS
33 47
98291
RUCM
CHRHNEL
I NDEX 1
S-RMT=
1
NRME
1 UCM
TOTRLS
1932 MRR 10 14=26= 12
RUN 47
FILE 2
METHOD 5
SRMPLE 4852 4 D 1S
*
CONC
XF=
1
RT RRER
KF
. 051 268. 5
8.426
49 72 183
151 765812
24741
F
*
2936 2936 2936
268.9
789984
VAB.0001115791
%
RUCM CHANNEL INDEX NAME
1
UCM 3
TOTALS
1982 MAR 10 11542:84
RUN 3
FILE 2
METHOD 5
CALIBRATION
CONC
RT AREA
KF
142
49 71 102
261 418933
10619
L >
2950
142
429753
A4
NEW FILE NAME UCM
RT 71
KF 2950
ROL UCM CHANNEL INDEX 4 NAME
1
UCM TOTALS
CQNC
73 73
RT 44
AREA
114 L 485531
405645
KF
1 ,I 7U0
0
RUCM
CHANNEL
o
I NDEX
o
RUN 4 CALIBRATION
1982 MAR 10 11:45:07
FILE
METHOD
NAME
CONC
RT AREA
KF
1
UCM
43 142
14
71 415081
29^
101
10397 >
VAB.0001115792
CHANNEL 2
RUN 2
f
H o H
r3) w
cn
C-4 C-4 *fc- t- ih)ll * K) "-J O C-4 C-4 OS CO VO
C -4 -
Q* k"'I cAo A
Q '0
C-4 Cfl hj
cr> W Q
to
K-t -p
* C-4 C-4 -J
~n T1 r~ *n
to K) Is) K'
* vD VO
C-4 cr>
C-4
C(T-4.
C-4 CTn
n
r-o a?
C-4
Ch
FILE 2
METHOD
- ' VAB.0001115793
-.i-PNN-hL 2
RUN 29
FILE 2
METHOD 5
INDEX 1
SRMPLE DM1
3.RMT=
1.597
XF=
1
NAME
CONC
RT BRER
KF
1
O
ucr*r
4 5 6
.831 .813 63.84 .911 1.779 .448
48 58 71 87 162 115
145 60
295623 4273 8342 2182
F F F >
2936 2936* 2936 2936 2936 2936
TOTRLS
bb .21
%
318545
RUCM
1982 MAR 10 13:36:55
CHANNEL 2
RUN 38
FILE
METHOD 5
INDEX 1
SAMPLE DM2
S. AMT=
1.469
XF=
NAME
CONC
RT AREA
KF
1 2 UCM 4 5 6
.825 .027 59. 16
uO"i?
1.654 . 417
48 58 71 86 101 115
186 116 255228 3755 7133 1881
F F F >
2936 2936 2936 2936* 2936 2936
TOTALS
62. 15
263131
RUCM
*
CHANNEL 2
RUN 31
198!2 MflR 18 13:48:38
FILE
2
METHOD 5
INDEX 1
SRMPLE DM3
S.RMT= NAME
1.493 CONC
KF =
*
1
RT AREA
KF
1 2 UCM 4 5 6
.829 .817 59.44 . 373 1.742 . 417
43 58 71 37 101 115
126 75
260581 3325. 7638 1327
F F
F
>
2936 2936 2936 2936
2936
TOTALS
62. 51
274077 ,
--
VAB.0001115794
TOTRLS
*
I
4G52
660101
NEW FILE NOME UCM
RT 303
KF 162-9
RUCM CHANNEL
2
RUN 43
MAR 10 16s 58s 44
FILE 2 P
METHOD 5
NAME
1 UCM
3 4 5
TOTRLS
CONC
.092 61.56
3.539 5- 143
. 543
7. S3
RT
49 1
36 102 112
AREA
345 230237
13237 19261
2050
F F F >
265130
KF
2936 2936 2936 2936 2936
ROL UCM CHANNEL 1 INDEX 2 NAME
1 o
RUN 93 CONC
4 UCM
TOTRLS
4691 4691
1932 MRR 18 lb* 55* 44
FILE 5
METHOD 5
RT
29 50 134 194 382
AREA
441 134
54 1560 764065
%
766254
F L
y *
KF 162.9
A VAB.0001115795
SAMPLE 62
MAR 10 17:06509 METHOD 5
CONC
.075 42.05
2.089 3.414
1. 'W*
47. 93
RT
49 72 87 183 112
RRER
266 149744
7439 12160
1114
S %
F \
178723
2936 2936 2936 2936 2936
FILE
MRR 10 2 METHOD
CONC
.07 40.27
2. o41 1. l%it'
. 19
44.01
RRER
A
'* A
VAB.0001115796
O RLJH 31
1932 MRR II 12=21:03 METHOD 5
SRMPLE ERR 3-1
1.261
KF 1
COWC
0w> 1
226 91.3
7.279 2.67
. 444
. %_f i'
102.5
RT
ZCf
43
I
37
102
113 116
RRER
115
0*v
36323 26354
y52
1639 2102
r-I7Q-> l Q
F > F F
>
KF 2925
29^5
JI
>
1932 MRR 11 12:23:55
2 RUN 32 FILE 2 METHOD 5
SRMPLE EPR 3-2
. 313
KF=
1
CONC
RT RRER
KF
. 044 . 253 . 023 90.25 7.433 7.402 1.317
33 49 33 72 37 102 113
106* 617
56 215935
17300 1 *' 15
3151
F > F >
2925 2925 2925 9**Q^OjChW*. 2925 2925 2925
10t>.
255430
1932 MRR 11 12:26:39
RUM
** %
METHOD 5
SRMPLE
WoiXc;
EPR 3-3
CONC
RT RRER
* ** 4
F
F
F
J OCr"cr
VAB.0001115797
<7 1>
*f
ROL UCM
CHANNEL
1
INDEX 4;
NOME
1
UCM
T QTALS
RUN 7a *u0
1982 MfiR METHOD ft
ROL UCM
CHANNEL
1
INDEK 43
NAME
UCM
TOTALS
ROL UCM
CHANNEL
*
INDEX
NOME
RUN 79
1932 MfiR 10
CONC
J
RT
AREA 745202 745202
l MAR METHOD
CONC
TOTALS
A
VAB.0001115798
ROL UCM CHfiNNEL
f*
1
RUN
75
INDEX NR ME
44
1
CONC
1 UCM
p * *
TOTALS ROL UCM
CHANNEL
1
4
>
RUN
77
INDEX 46
NRME
CONC
UCM
19S2 MAR 18
FILE
METHOD
RT 44
ftREB
138 96183
\
y
KF
i;70
FILE 5
METHOD 5
RT ftREfi
TOTftl-S
CHfiNNEL
1
INDEX 39
NAME UCM
TOTALS
RUH 78
FILE
5
METHOD
CONC
RT 299
ftREfi
*
w
*
384566 >
KF 1 78
384566
ROL. UCM
CHANNEL
1
INDEX 41
HR ME
1
UCM
TOTALS
RUN 72
1982 MftR 10
FILE
yj
METHOD J
COHC
RT
47 382
ftREfi
49 L 81469 >
381518
KF
i 70
AI W
* *I
*
VAB.0001115799
RGL UCM
CHANNEL
i
INDEX 5
HOME
h
1
UCM TOTALS
UCM CHANNEL 1 INDEX 51 NAME
1
UCM TOTALS ROL UCM CHANNEL 1 I NDEX NAME
1
UCM TOTALS
RUN o 1
1982 MAR 1QT METHOD
CONC RUN
RT AREA
47 12 1
248 45
607 1117242
L
>
1118142 1982 MAR 10
FILE
wl
METHOD
CONC
RT AREft
143
7025 L
296 1898791 V
1105816
RUN OT
CONC
i
VAB.0001115800
t
ROL UCM
CHANNEL 1
INDEX 60
NAME UCM
totals
*
RUN 91 CGNC
1982 MRR 10
FILE J
METHOD
**
RT 305
BREA
*
647915 >
KF
647915
%
ROL UCM CHANNEL 1 INDEX 61 NfiME ULM
totals
RUN 92
CONC
19;S2 MAR 10
FILE 5
METHOD
!
RT 305
AREA 660185 > 668105
tKF
:OL UCM HAN NEL N l.*EX SAME
-1t o
1
4 *CM
OTALS
RUN 93 h
1982 MAR FILE 5
10 *
METHOD -
5
RT
29 5S 134 IP*
AREA
441 134 54 1560 764G65
F L
>
162. ^
Se>Y 4 < 7~r
*t oti
*a
K
VAB.0001115801
B1- f
ROL UCM CHRNNEL 1 INDEX 33 NAME UCM TOTRLS
RUN CONC
1932 MfiR 10 J METHOD yj
RT 99
RRER 3201 3201
>
KF
I
lz*
k)
ROL UCM
CHANNEL
1
INDEX 39
NAME
UCM
TOTRLS
RUN CONC
w L
1932 MflR 10 yj METHOD sJ
RT RRER
l4 Ut111
S14566
KF
*' *
' t
VAB.0001115802
4 tL> fS>m 3
ROL UCM CHANNEL
I k IT'jw i n-^Ci 'i
NAME UCM FOTALS
L UCM ANNEL DE X M M TRLS
1 1
ROL UCM t* CHANNEL * 1
INDEX
hi it ii_
UCM
T OTALS
RUN
I
1932 MAR 11 METHODI
COHC RUN t-
RT AREA 38 61750
61750
KF
1932 MAR 11
FILE
METHOD ji
CQNC
RT
02
AREA 264510 >
264510
KF
RUN 95
1932 MAR 11 FI METHOD
CONC
i
RT 302
AREA
/ 502405V7 >
50248 I
KF
4
ri
f h
ROL UCM CHANNEL INDEX 1 'll li iL UCM TOTALS
1
F
RUN 96
1982 MAR 11
FILE 5
METHOD 5
CONC
RT
362
AREA
r
510652 >
518652
TM
KF
m
.
7u
VAB.0001115803
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NAME
1
RUN CONC
1982 MRR 11
FILE J
METHOD
RT flREft
KF
rOTRLS
ROL UCM
CHftNNEL
1
INDEX 3
NRME
1
*"r *
T
4 UCM
TGTftLS
RUN 4
1932 MRR 11
FILE 5
METHOD 5
CONC
*
RT RRER
29 58 134 194 296
622 140 135 7503 2935021
F L
>
2993421
w
KF
CHANNEL 1 X NDEX 4 NRME
J
RUN 5
FILE
MRR 11
5 METHOD 5
--
CONC
RT
26 50 143 191
296
RRER
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VAB.0001115816
REACTOR OPENING LOSS CALCULATION
Data
3
Volume of reactor, V 4,487 ft. Barometric pressure, P = 30.08 in. Hg. Reactor temperature, T =* 582R
Molecular Weight of VCM, M * 62.5 lb.
lb.-mole
Gas Constant, R = 21.9 (in. Hg) (ft.3)
(lb.-mole) (R)
Density of VCM at reactor conditions, D
D = PM
= (30.08) (62,5) - 0.147 lb.
RT (21.9) (582)
ft.3
Fraction of water vapor in reactor gas, W = 0.122 FVC Production, Z = 56,986 lbs. for 5265 resin
64,521 lbs. for 5385 resin
Concentration of vinyl chloride in reactor3
C *=
6368ppm for batch 745 - 155
4823ppm for batch 745 - 156
= 23357ppm for batch 745 - 157
dry basis,
C
Reactor Opening Loss Calculations
The reactor opening loss, R0L, is calculated by the following equation.
ROL = (C) (1-W) (V) (D) (Z)
- (ft.3 VCM)
X (ft'.j dry gas)
x
(MM ft.J dry gas)
(ft.""" reactor gas)
(lb. VCM (ft.3 VCM)
x (1)
= lbs. VCM
lbs. PVC
MM Lbs. VCM
reactor gas) X
Batch No. 745-155
ROL = (6368) (1-0.122) (4.487) (56,986)
= 65 lbs. VCM MM lbs. VCM
(0.147)
A
VAB.0001115817
* * * /
REACTOR OPENING LOSS CALCULATION (Continued)
Batch No. 745-156
ROL = (4823) (1-Q.122) (4.487) (0.147) (64,521)
= 43 Lbs. VCM MM lbs. PVC
Batch No. 745-157
ROL = (23,357) (1^0.122) (4.487) (0.147) (64,521)
= 210 lbs. VCM MM lbs. PVC
A
VAB.0001115818
A
TO: BRENDA
FROM:
PLEASE ADD THE FOLLOWING ENGINEERING FILE:
FILE TYPE: (check one)
0*;
CORRESPONDENCE
DATE
PROJECT
ADD FILE UNDER THE FOLLOWING MAIN HEADING: (check one)
1.0.0 2.0.0 3.0.0 4.0.0 5.0.0 6.0.0 7.0.0
AFE REQUESTS & BUDGETS VINYL DRYERS COMPOUNDS DRY BLEND PLASTICIZER UTILITIES & AUXILIARY FACILITIES
JL 8.0.0 9.0.0 10.0.0 11.0.0 12.0.0 13.0.0 14.0.0
ENVIRONMENTAL ENERGY CONSUMPTION SAFETY ACCOUNTING BUSINESS AREA QUALITY ADMINISTRATION
SHOULD THIS FILE GO UNDER A SUB-HEADING? IF SO, GIVE FILE NUMBER AND NAME:
9 I
A********************************************************************************
V
rV
\
VAB.0001115819