Document 2Og3MYv5Lqr01mrEJB8rjZgg
CELANESE CHEMICAL COMPANY Chemcel Plant Bishop, Texas
To: Dr. R. R. Graham From: G. D. Boyd
GDB-131-81
August 10,1981
Laboratory Department Summary July, 1981 '
Chemical
J. J. Fritsch W. H. Brough J. B. Brown R. R. Carpenter M. W. Clifton R. S, Hahn W. A. Heenan A. A. Miller B. C. Kerr C. W. Lee D. E. Lockwood R. P. Lowry A. G. McGehee W. H. Meyer D. G. Pausky 0. W. Schnellenberger G. R. Scholz D. D. Siemonsma W. L. Sharp K. R. Stelts H. H. Thigpen
DISTRIBUTION
Plastics
R. G. Brandt A. C. Abshier R. L. Bunkley H. L. Davis D. A. Reck E. J. Heinz
CCCTC
G. J. Fisher W. E. Heinz W. T. McNair Central Files
(2)
J. N. Gann, Bay City J. E. Sanborn, Bayport J. L. Paul, Clear Lake W. H. Tuke, Pampa T. H. Golson, Dallas
003548
File No: 303.3
auGi0 8i
CELANESE CHEMICAL COMPANY Chemcel Plant Bishop, Texas
To: Dr. R. R. Graham From: G. D. Boyd
GDB-131-81
August 10, 1981
Laboratory Department Summary July, 1981
A summary of each group's monthly report is attached. Section I contains a summary of the Quality Assurance and Analytical Group activities with tables of analytical statistics, shipments, quality waivers, quality complaints and sample shipping statistics. Section II describes the status of Special Prob lems Groups and Staff Chemist projects by chemist assignment. A table listing the priorities, justifications, and estimated completion dates of current Special Problems projects is also included in Section II.
GDB:jr
G. D. Boyd
003549
GDB-131-81 Page Two August 10, 1981
HIGHLIGHTS 0 The Hooker Chemical Co. (North Tonawanda, N.Y.) formaldehyde color
problem is due to high levels of filterable iron. This problem appears unrelated to MO product color excursions. Recent positive fecal coliform tests indicate that chlorination of the BOD outfall should continue. Polyol and VCI waste treatability studies are underway. Redox potentials of groundwater monitor wells 3,4 and 6 showed negative values from -200 mv to -510 mv. Negative redox potential is indicative of anaerobic bioactivity.
003550
GDB-131-81 Page Three August 10, 1981
I. ANALYTICAL GROUP
Methanol Oxidation (MO)
Analytical support was provided for a rate run on MO units II and III. The samples were analyzed for methanol, water and formaldehyde content. The purpose was to establish rates and efficiencies with the crude methanol feed and to identify production bottlenecks. Process Engineering will publish a report.
Utilities and BOD
The Laboratory has begun routine determination of fecal coliform bacteria count in the Plant 101 outfall on a weekly basis. The purpose of this work is to monitor the effectiveness of the chlorination system and to determine when and if chlorination can be discontinued.
A study is underway to determine the 5 day BOD reduction across the anaerobic filter. This is to provide information to the Dallas Aerobic Mar keting group.
Special Analytical Assignments
MO Formaldehyde Impurities and Color (F. R. Dow, B. W. Wise) - Formalde hyde from MO II and III had APHA colors from 5 to 15 during July. GC Cap illary Column and LC analysis was performed on several series of samples in an effort to determine differences between units. The investigation is still underway, but the following observations have been determined:
1. Formaldehyde product has more impurities than expected not necessarily related to crude MeOH feed.
2. MO II and III have more impurities than MO IV. 3. The full adverse effect of T-185 OH and T-240 OH addition to MO II and
III is not known. 4. LC and wet chemical analysis confirm the presence of unsaturates in
streams around MO II and III. 5. Formaldehyde product (T-185 Res.) from the weak formaldehyde recovery
system may cause UV absorbance problems associated with PE. 6. 2-Ethyl-2-hexenal (impurity from TMP) was present in MO III product
during the July 10, 1981 formaldehyde color problem.
This investigation is still in progress. A report will be issued detail ing the final results.
Customer Comolaints
1. 7-81 - Hooker Chemical Co. - N. Tonawanda, N.Y. - has complained of 6 more 50% HCHO tank cars arriving with a "yellow" color (est. 25-40). With
003551
GDB-131-81 Page Four
August 10, 1981
the one Acme Resin and two previous Hooker color complaints, listed in the June report, this- brings the recent color build complaints of external customers to nine*; Returned samples are in route.
2. 7-24-81- Argo Terminal-Chicago, Illinois - Compalined of a tankcar of 37.7 HCHO arriving with a color of 35. This is the first instance of a lower blend, or inhibited, color complaint. It is not known if the complaints are related. A sample is being returned for evaluation.
Quality Waivers
1. 6-30-81 - Para F-Powder - 40,000 lbs. to Du Pont (export), iron 2.6 ppm vs. max. spec, of 2.0-SQD.
2. 6-30-81 - Para C-Powder - 45,000 lbs. to Davis Mud and Chemicals, Great Bend, Kansas, iron 2.4 ppm vs. max. spec, of 2.0-SQD.
3. 7-1, 7-2, 7-9-81 - n-Butyl Acetate - 589,730 lbs. to Celanese Bayport Terminal - Iso-Butyl Acetate content at 0.12 to 0.19 wt.% vs. max. spec, of 0.10-QD.
4. 7-7, 7-8-81 n-Butyl Acetate - 595,050 lbs. to Celanese Bayport Terminal, Iso-Butyl Acetate content at 0.12 to 0.19 wt.% vs. max. spec, of 0.10-QD.
5. 7-21-81 - n-Propyl Acetate - 7,120 lbs. to Delta Solvents, Dallas Texas - Water content; at 0.18 wt.% vs. max. spec. of 0.10-SQD.
Product
% QD1 Month
% QD YTD
% SQD2 Month
% SQD YTD
Para F-?owder Para C-Powder Diacetone Alcohol Formaldehyde n-Butyl Acetate Sodium Formate Pentaerythritol-Tech (Lube Grade as Tech) Iso-Butyl Acetate n-Propyl Acetate
0 0 0 0 33.7 0 0
0 0
1.4 15.0 0 52.9
0.6 0 0.2 0 6.1 0
00 00
3.5 8.0
0 0 2.0 1.5 1.6
3.9 0
0
0 1.3 <0.1
1 Lbs. of product shipped out of Manufacturing Control Specification vs. total lbs. of that product shpped for Month and YTD.
2 Lbs. of product shipped out of Sales Specification vs. total lbs. of that product shipped for Month and YTD.
003552
Sample Count Chemical Section Instrument Section Total
Technician Overtime Chemical Section Instrument Section Total
Sample Shipping Domestic Export Plastics Others Total
QA Statistics Shipments Waivers (QD) Waivers (SQD) Complaints
Analytical Statistics
July-
July YTD
3966 3018
6984
31811 18876
50687
28 460 46 260
74 720
75 438 6 36 29 7 66
90 549
597 ' 5 3 4
4604 15 8 9
Previous YTD
33123 17001 50124
539 239 778'
475 16 55 50
596
5543 7 4
23
003553
GDB-131-81 Page Six August 10, 1981
II. SPECIAL PROBLEMS GROUP
Process Technology B. C. Kerr
WMSTF Work - Minor support work continued in support of Process Engineering cursory design work. A sample of Pond 10 & 11E was sent to De Leval for centrifuge studies.
A trip was made to Austin to review monitor well analytical data and agronomy studies with UEM, Inc. personnel. URM, Inc., believes it is im portant to continue the sampling and analytical program for monitor wells for the remainder of 1981.
Process Technology Manual Revision - Draft revisions for approximately one-half of the manual have been completed and Mrs. Ralston is essentially current on typing the drafts for approval.
A target date of November 18th has been selected for completion of this project.
Formaldehyde Color Problems - MS Unit data are being examined to deter mine if there is any correlation with MO Unit color problems.
Methanol Oxidation, Formaldehyde Blending T. A. Jasek, D. T. Biernacki, J. F. Glenister, J. D. Presley
Formaldehyde Color (Jasek, Glenister) - Work continues in an attempt to identify the source(s) of color in the formaldehyde product.
There is some indication that a color precursor may exist in the methanol feed to the MO units. A series of distillations are currently being conducted to concentrate the various impurities present in the feed methanol. T-185 OH the Weak Formaldehyde methanol recovery stream is also being analyzed. A sample of T-185 OH has been sent to CCCTC for GC/Mass Spec analysis. Also sent for analysis is a methylene chloride extract of formaldehyde which had a color of 13. A status report on this color problem is being written.
MO Color Development Testing (Presley) - Recent customer complaints (Hooker Chemical Co) of highly colored HCHO (20-35 Pt-Co color units) led to an examination of possible storage problems at Bishop. Color development samples were set up in a 155F oven using HCHO from the Blending Unit (V-619, 7-2305, and 7-2484), MO 17 (7-692 and 7-1745) and MO III (7-1701). The Blend ing Unit tanks `represent HCHO that has been treated by the anion beds to remove acid and has had metalose added. The MO III and MQ 17 tanks are raw unit products.
Samples from all of these tanks have been taken at various intervals over a three week period. The colors are read on the samples initially and at three day intervals for a total of 21 days. To date, none of the
003554
GDB-131-81 Page Seven August 10, 1981
samples have shown significant color build. Only early V-619 samples went off spec. (spec.-is- 10 Pt-Co units) colors which started at 6-8 and rose to 13-15. At this indication, V-619 was emptied and cleaned. Recent samples (since the clean-out) are still being evaluated, however, the early samples still have stable color at 13-15.
Additionally, color development tests have been set up to study various samples taken around the Blending Unit and the Tank Car Cleaning Racks. Under evaluation are both soaps, (Electrosol and Spillclean) used at the Cleaning Racks. No color was developed in Blending Unit HCHO containing ^1500 ppm of these soaps after 4 days at 155F. Also tested were anion resins taken from the.back-wash shaker, and three resin and sand samples and one wall scrap ping taken from V-619 when it was cleaned. Samples containing resin (1500 ppm) experienced a slight color rise from <5 to 7 after 4 days at 155F.
Plans are to determine color build with tank car lining material. Testing will begin when treated coupons are available.
HCHO Customer Complaints (Presley) - A complaint of off color HCHO (37% HCHO/7% MeOH) was received from the Argo Terminal in Chicago. The HCHO at Argo (CELX 1523) was originally reported to be a 35 color. Much of this color was determined to be haze. A sample returned to Bishop had a color of 12. It was found that the color could be reduced to <5 by filtration through a 0.45 micron filter. The material on the filter was analyzed to be mostly a particulate iron compound. Total iron in the sample was determined by AA to be 0.22 ppm (0.17 ppm was filterable).
High color HCHO (50%) complaints have continued from Hooker Chemical Co. Two tank car samples sent back from Hooker contained high levels of iron (by AA) . CELX 13203 had 5.4 ppm iron and CELX 13209 10.6 ppm iron. Levels of other metals are currently being checked. Using a combined filter system (a 5 micron and 0.45 micron), the color can be significantly reduced in the samples. CELX 12203 went from unreadable to a 6 color and CELX 13209 went from unreadable to an 18 color. Work continues.
Crude Methanol (Jasek, Biernacki, Glenister) - The Laboratory continues to provide Operations with methanol losses out the absorber vent.
Laboratory MO Micro Unit (Jasek, Biernacki) - After some initial problems with the unit efficiency, the microunit is operating well. Several new silver catalyst samples have been evaluated to establish a base case. Work is just beginning on the effects of ultrasonically cleaned silver catalyst. No conclusions can be drawn, yet.
Formaldehyde Stabilizer Study II (Day) - A letter is under review which documents some of the follow-up work from a set of stabilized HCHO samples made up on January 21, 1981. (RLD-21-81)
The study done in January is referred to here as Study I. The follow-up work is Study II.
These conclusions can be drawn based on the set of stabilized HCHO samples of Study II prepared on June 19, 1981:
003555
Page Eight August 10, 1981
1. The polyvinyl alcohol (PVOH)/metalose stabilizer mix is as good as the metalose stabilizer alone, but not better. Higher concentrations of the stabilizers than in Study I were tested, as well as different concen tration and ratios of PVOHimetalose, but the stabilizer mix still did not have synergistic effects on stabilizing HCHO.
2. The optimum level of metalose stabilizer for HCHO shipments is probably 12-14 ppm. The average level of metalose in HCHO shipments in 1980 was 12.7 ppm.
3. At the optimum stabilizer concentration for HCHO shipments (12-14 ppm), a reduction in stability of the HCHO samples -in Study II was seen as com pared to the previous set of samples in Study I. This reduction in stability was most probably due to differences in the HCHO itself. The known differences between the HCHO used for Study I and Study II, were that, for Study II, the HCHO was colored (10 Pt-Co Units) and had been produced during the current run to feed crude methanol to the MO Units.
Future work involves determining the reason for the current reduction in
HCHO stability. In Study I it was found that HCHO directly off the finishing
column, T-272, in MO IV had longer stability times than HCHO which had passed
through the ion exchange resin bed. Possible reasons are sodium contamination
from the resin bed- acid concentration differences, and age differences of the
HCHO.
'
3oth the additional follow-up work and future work planned will be done on a part-time, low priority basis.
MO Unit Support (Glenister, Jasek) - The Laboratory conducted analytical AMR's at MO II "A" train on July 30, 1981:
Indicated
.85-.93 .85-.93 .80-.85
.83-.87
AMR Analytical Startup 1.83 1.47* 1.29 Rate Up 0.91
* Increased flaw rate to WTM.
Dow XFS-43223 Evaluation (Glenister) - The Laboratory evaluated the total capacity of Dow SFS-43223 as a replacement for SFS-4048 in the Blending Unit. In an abbreviated method, the total capacity was determined to be 1.43 meq acid/ml resin versus the manufacturers stated value of 1.5 meq/ml resin. Operations will request information from Dow about "color throw" and bulk density of the SFS--43223 compared to SFS-4048.
003556
GDB-131-81 Page Nine August 10, 1981
BOD, Utilities i P. W. Young, D. R. Akin
BOD II Support (Young) - Continued support was provided to BOD II Operations. The cause of high outfall COD (s240-250 ppm) is being investi gated.
Fecal Coliform in 101 Outfall (Young) - The 101 outfall continues to be chlorinated to maintain fecal coliform less than 200 count/100 ml. Weekly sample of 7-6 showed 200 count/100 ml in 101 outfall before CI2 . The sample of 7-13 showed not only 200 count/100 ml before CI2 but 100 after CI2.
Polyol Treatability in BOD II (Young) - A Laboratory anaerobic-aerobic system is currently being fed a feed in which 4% by volume (23% COD) is polyol steady state effluent. Operation is at current BOD II organic loading of 0.2 lbs COD/ft /day. Outfall COD is 250 ppm at an aerobic detention time of 3.5 days. The concentration of polyol waste will be further increased.
Polyol unsteady waste streams are being sampled and analyzed. These data will be used to formulate a treatability study of the unsteady state . streams. A report documenting previous laboratory studies of polyol treatability is being written.
VCI Waste Treatability (Young) - VCI waste is being fed to a laboratory anaerobic-aerobic system at a feed concentration of 4% by volume (10% of COD). At an OL = 0.2 and detention time of 3.5 days, the outfall COD is 120 ppm. The concentration of VCI waste will be increased to simulate what would occur if the waste were fed to 30D II.
BOD II Aerobic Optimization (Young) - Three aerobic systems are being operated to find the optimum sludge age for the BOD II aeration basins.
Sludge Disposal - Aerobic Digestion (Young) - Two aerobic digestors are being operated in conjunction with Environmental Dynamics, Inc. to support evaluation of sludge disposal alternatives.
TPP and TPPO (and PuQio) Emissions from the Waste Liquid Boiler (Akin) A procedure to extract TPP and TPPO from -the acid scrubber solution (after neutralization) with an organic solvent has been developed. By concentrating the organic extractant and analyzing on a gas chromatograph equipped with a thermionic specific detector one can detect TPP and TPPO concentrations of 1 ppm or greater in the stack gas. This GC method has also been developed. CCCTC will analyze the acid scrubber solution for total phosphorus by atomic absorption. By_ taking the total phosphorus level and the total TPP and TPPO levels one can determine the P^Om level by difference. The waste liquid boiler is currently being studied to determine the best possible sampling location.
Reoccurrence of GE-60 in Plant Nitrogen Lines (Akin) - The liquid found in the Plant nitrogen lines on July 6th was determined to be a dilute mixture of GE 60 in water. Since this date no further contamination has occurred.
003557
GDB-131-81 Page Ten August 10, 1981
High Silica -Levels in the Boilers (Akin) - Silica levels in the 240 lb. steam boiler vhave been higher (>35 ppm) than recommended operating concentrations. The Laboratory has been monitoring the silica levels from the demineralizer to determine why the levels have been higher than usual in the boiler. Work will continue.
WMSTF Support (Akin) - A study is underway to determine if sludge to be landfilled in the future will be a hazardous solid waste. This study encom passes the toxicity and corrosivity of the landfilled sludge. This study will continue.
Methanol Synthesis J. C. Bustabad
Reprocessing of Contaminated MeOH in V-645 and V-650 - Laboratory distillations were completed on crude methanol for base case data and crude methanol blended with contaminated MeOH from V-650 in the ratio of 14.9/1. Plans are to complete the analyses of the different streams and issue a letter next month.
Preparation for Plant Trial of Sodium Metavanadate as a MEA Corrosion Inhibitor - A Plant trial using sodium metavanadate (NaV03) as a MEA cor rosion inhibitor was planned at a July 7th meeting of Process Engineering, Plant Engineering, Operations, and Laboratory. Laboratory evaluation of a sodium metavanadate method to be used for monitoring inhibitor concentrations during the Plant trial showed an accuracy of 3% of the concentration number for ranges of 500-1000 ppm NaV03. Less accuracy was encountered with a 100 ppm NaV03 in MEA sample. Work will continue with lower NaV03 concentrations (50-250 ppm.)
Monitoring of H2S in Recycled CO2 - July 16th and July 31st checks by Drager showed undetectable levels of H2S in 5MM Girdler, 2MM Girdler, and Shift recycled CO2 streams.
Evaluation of Solids from HE-2552 - Solids seeping from HE-2552 (MUG interstage trim cooler) were identified as predominately iron, indicating corrosion associated with the heat exchanger.
Qxo Butanol J. D. Presley
Reactor Stability Accountability - Fluctuations of TPP concentration are still being experienced. The problem seems to be partially related to the GC method. Some improvements have been made to stabilize readings. Average monthly accountability is still excellent, 89%.
Rhodium Accountability - July rhodium accounting is still good for Run VII, 88% by analysis. It is believed actual accountability would be higher if a static reactor level could be measured. Rhodium loss out T-210 Res. RTD is 6.06 pounds.
003558
GDB-131-81 Page Twelve August 10, 1981
Studies are~in progress to determine the feasibility of obtaining a PE with a high di-PE content through screening of Tech-grade PE, Results will be published in a letter with Operations in August.
Formation of Pormals in the HCHO Stripper Column (Smith) - The formation of additional formals in the PE HCHO stripper column (T-286) is being investi gated.
Minimizing UV Absorbance of Pure PE at 220 nm (Huelle) - The Pierce Chemical Company method of sugar detection was not useful in determining sugar precursors. The GC method does not separate Ci to Ci, compounds. George Blay from the Analytical Section of the Tech Center has suggested an alternative method. I am currently working on a revision of the alternative method and trying to identify peaks detected. The Pure PE run now in progress has consistently produced low UV absorbing product, making it difficult to correlate HCHO GC peaks to high UV absorbance. Work will continue.
Trimethylolpropane R. L. Day, S. G. Smith
T-312 Extractor Optimization - Base Case Data (Day) - A letter is under review documenting base case data gathered on the IMP T-312 extractor in July and December, 1980.
Future work involves Plant trials to evaluate changing the temperature(s) of the feed(s) to the extractor to reduce the ethyl acetate and TMP losses in the residue. Data indicate that increasing the temperature of the ethyl acetate solvent feed will reduce both the TMP and ethyl acetate losses in the residue.
A meeting with Production, Process, and the Laboratory will be held to discuss future work.
TMP Reactor Scale Buildup (Day) - At the request of J. Thomas, CCCTC, samples (1 lb.) of the TMP tubular reactor scale were collected during the TMP Unit shutdown and sent to the Tech Center on July 14, 1981.
Every time the TMP Unit is down, the scale buildup is soaked in ethyl acetate then water blasted from the reactors.
This scale buildup was the worst on the top two or three rows of the reactors, where it was 31/2" thick. The scale has a rubbery texture. The side facing the walls of the reactor is different in appearance from the side facing the reactor core.
Analysis in the Bishop Laboratory showed the scale to be roughly 5%. inorganics.
The Tech Center is working on a method to remove the reactor scale buildup that may be superior to the current method.
003559
GDB--131-81 Page Eleven August 10, 1981
Improved Rhodium Recovery - The 202 phosphoric acid (H3PO4) treatment followed by two water washes has been confirmed in successfully treating Run VI MEA contaminated' Oxo catalyst. The acid treatment causes a slight volume loss of the catalyst being treated with a corresponding increase of rhodium. This loss of volume is presumed to be dissolved water in the catalyst going to the H3P04 phase. As a check, rhodiums in the acid phase anH the two water washes were determined and found to be 16-18 ppm, 2-3 ppm and 0.5-1.0 ppm, respectively.
Confirmation of the catalytic activity after acid treatment and 1:10 (catalyst:solvent) extraction with propylene was also made. Previously, the catalytic activity was shown to 0.91 liters/mole-sec. The confirmation testing yielded 0.89 liters/mole-sec.
Foaming tests were attempted as with previous samples, however, results were still inconclusive. Plans are to send samples of treated and untreated Run VI catalyst to CCCTC for Micro Unit rousing tests.
Work Continues.
Acetates, Paraform, Formcel Products J. E. Russell
Unit Support - None provided.
1,3-Butylene Glycol J. E. Russell
V-778 Residue Burning - A letter was published (JER-29-81) documenting the results of V-778 residue analysis. The average of the 13 samples taken during May and June showed an ash content of 3.29%. This should be a repre sentative value of the ash content for V-778 Residue over a period of time.
Pentaerytnritol L. M. Harvey, B. K. Huelle, S. G. Smith
Recovery of PE From VCI Extraction Waste Stream (Harvey) - VCI began operation of their bench-scale extraction unit on July 27 to investigate the effect of various solvent ratios on extractor efficiency. The organic extract from their 3-day study has been obtained for Bishop Laboratory studies to recover PE. Work is in progress.
Determine Potential of PE Dust for Use as Lube-grade PE (Harvey) Characterization of PE Dust (collected in Hopper #4 over a three-month period) by composition, particle size, ash and moisture has been completed. Di-PE content of the dust varied from 18-31 wt.%. The ash and moisture content exceed the specifications set for Tech-grade PE (0.01 wt.% max. ash, 0.30 wt.% max. moisture). A report is being written with Operations.
003560
GDB-131-81 Page Thirteen
August 10, 1981
Methanolysis. of IMP 747 Residue (Day) - A recent economic evaluation of the methanolysis bf TMP 747 Residue scheme proved unfavorable. A review of the original Laboratory work showed that only a 2.5:1 molar ratio of methanol to bis TMP mono linear formal was utilized. If this ratio can be dropped (i.e., 2:1) and still maintain a comparable conversion to TMP, then this would improve the economics considerably.
After the methanolysis step in the original scheme, the methanolysis product was extracted with T-312 residue.
The result was a two-phased system. The organic stream was to be burned. However, later economic evaluation showed this stream to be too high in salt content. If the amount of methanol used can be dropped enough, it is possible that the salt content of this organic layer will also drop.
The water layer resulting from the extraction step was to be sent to T-202 to remove the excess methanol. However, if the methanol usage is lowered so that minimal excess of methanol exists, then it may be possible to return this stream directly to the T-312 extractor. According to the original Laboratory work, this stream would have a composition comparable to the stream that currently feeds the extractor (except for the methanol) .
Work is currently underway to determine if lowering the molar ratio of methanol to bis TMP mono linear formal is feasible.
Formation of Formals in the TMP HCHO Stripper Column (Smith) - The formal content of TMP HCHO stripper column (T-202) residue was compared to that of T-202 feed stripped of HCHO under "mild" conditions in the Laboratory. No difference was observed between the feed and residue.
Miscellaneous J. E. Russell, D. R. Akin
Redox Potential of Monitor Wells - The redox potential of the liquid in monitor wells 3, 4, and 6 was measured in response to a request from CCCTC. The wells had a nitrogen purge to exclude oxygen from contacting and dis solving in the liquid. The potentials ranged from -200 mv to -510 mv in depths from 2 ft. to 17.5 ft.
Samples of the nitrogen blanket were analyzed for methane. The nitrogen from monitor wells 3 and 4 showed methane was present (0.2-0,3%). methane was detectable in the atmosphere above MW6.
No
' Environmental Health C. E. Gary, K. V. Parker
The follow-up personal formaldehyde exposure sampling is ^90% complete.(KVP)
The use of infrared analysis to test for asbestos in insulation was demonstrated and compared to wet chemical spot testing. (CEG, KVP)
003561
GDB-131-81 Page Fourteen August 10, 1981
A personal carbon monoxide exposure survey was completed in the MS and Oxo units. No problem eight hour TWA exposure was dound. (CEG-53-81).
The reaction at ambient temperature between formaldehyde (5-250 ppm) and ammonium salts ( 1%) and/or ammonium hydroxide (0.3-3.0%) is not quantitative and can not be used to determine formaldehyde exposures. (CEG-52-81)
003562
E s tim a te d C o m p le tio n D a te
S eptem ber l i 1981
C o n tin u in g r ,
S e p te m b e r, 1981 e N ovem ber, 1981
Ja n u a ry 1, 1982 S eptem ber 1 ,.1 9 8 1 S e p te m b e r 1 , 1981 O c to b e r 1 , 1981 S e p te m b e r 1 , 1981 S e p te m b e r 1 , 1981 S e p te m b e r 1 , 1981
'
3 0 w 44
ou
o Li 83 CL
Q
C S 0) ^4
45 0
>s 4p4* u 0 *4 4
(0 *p4 A
u
<U c. 44 CO CQ
> --4
<U
<u <
Li U 3 u
03 i*. r4 CO 4-1 CO
cj
<y
cn 4J
00 cO
c *H
c L*
> ai
c0 44
C/3
CO
3)
c0 03 H U
a) ^3 44 CQ CO 4J
CO
0) 5 03
C0 0 o
OS H Z
.3 H 03 03 O 04
U CQ
O 4J 44 c
<u cR o <u *H > 4-1 o c0 u
3 a.
rH CO H > w
O 44 c CQ 01
fH o c0 H 4-1 44 c0 44 cj W
a
44 2 01 > o u 04 M
O s 0} H U H 44 44 fc3
4-1 03 > rH CO 4J
aCO
^4 *-4
CM ^4
>> o
u 9} <5 CQ
<u
a
CO
ea c
CQ
u
>1 (U
d
CL, rH
o
-o c d
a 3 c CO
<u a)
oa
44
CQ
CL
>
rH
c
CUO o
CO 44
a CO
>
w H
> 44
c
a CO
3 O)
03
00 c
*cH *
a)
0u3 con
-U 03
>.
rH CO 44 CO cj
zo
Li o rH o
cj
-U o
-3a
a 3-i 04
a)
>r*
<u T3 t^4 CO Li o h
U Q 4-1 a C0
03
ai
c o H 4-1 CO
*d
* o
iH Co co 4J
CeUO
CO N H
z03 rt 4-1
CJ Q.
oo
4-1 CQ >. i--l c0 4-1 CO CJ
Li 0)
>
pH *H CO
*d 03 H 44
*d
zO
*d p C0
03 4J c a 03 00 <u c > *H O>
al-i. c(n0
MH
to >s *H a 1j c <u 03 4-1 H C0 cj Z
44 5 44 03 W
CQ M 0)
pH C. CL
c3n
0) 4J c0 c U <u 44 t-4 <;
CQ H rH ^5 CO 44 03 H
r4 ^4
34 <u 44 03 H /c <u --} a
03
4J
c
0)
03
>
oc 34 o
CL H
M
44 CO
0cHr0
i-34
CO
H>
03 CQ 44
3 <13
C(UQ
00 H
u
U <0
>
pH
4c4
cn cHn
c o *H 44
CO o H
44
*H
44
c CO 44
3 Li O' o
a
03 a
c 0
c3n
m Pl
03 *H
cHn
cs
w
44 O
c o H 44 d c H d 44 * C 44 O CQ CJ >>
Li CO 3 LJ U4 d i-l CJ
c3n u 03 <u (J Li 3O "O M4 <u <u ei oi
03 d o
44 03 2E
<44 o
c o H A4 d c . H O <a U Li <U 3 44 CJ 03 a
a<
CN ^4
p4 CN
c\ \ /
<5
c
o
H
44
CO
s
*H
u
9)
44
03 CJ
e CO o Li
H CO
03 jp
03 CJ
H
Ji
Wo
in
3 Li
oH
c4
a, 2
*
3 3
a. a
a. CQ
H>
n d
44 03
r3a
a . a>
<u
<u 3 d
44 a)
z
Li o <44
CQ 44
c
03 43 L O CQ
<
34 3 <44 rH
c3n ^
\ \ /
a
o H 44 d
^34 d>
Esl "d O 44 03
2
j*
>oo-
Z'
003563
<0
*3 Q 5C ca O " cc 'Uh w G) ca a. wa
u
CQ 44 V 03 n 0
Cm
CQ a
43 --H J 0
<Q
o m a CO
4J V
Cu 3 o
r* 4J 03 o r* V4 ** CQ 3 1--3
>* 4-i Cu o W tu CU
<+4 CQ 4 e <-- u
44 u o
o
ou
CM GO c\
A ^4
?N CU CQ 3 (Q
GO *
o> r-4
**4
* 00 CO Cl `
^4
u **"
a
03 u
jo E
*, V
JaO
<u o
> 4J
zo
a a
^4 CO c\ ^4
A
u 0) JO
2 <u XJ Cu <D cn
^4 *4
4
CO CO
a4 CO *4
a\ a\
- CO a\ oo
^4 60 A
^4 A
CO C\
a\ r-4
H A
a\ --4
c Cu
Cu
A Cu
A
H <U ai A u a) Cu
3 03 03 54 01
ai
E
<U JO
03
i-4 a) XJ XJ
3 XJ
X O'
6 <v
ai XJ
ai
a
cu XJ
>
a
>
z zO a>
CJ cn
<u o cn o
o
0) cn
o
00
03
ca
s H
Ou
T3 <u
c i--4
Cu
<3 3
JO d
o
o o 03
44
3= C
54
XJ CQ
0u
3 XJ CQ
03
03
i--1 *H
JO
CQ
0) 00
00
03
GO CQ r-4 Pi
c 00
53
3 CU
CQ
u H
H
E
*H
S3 S
XJ GO
T3
3>
> *rl
>
Q c 54
C
CQ CO >
CQ
3O
(U CU
<Q
cn ca
CQ
cn a)
00
cn
ca
/--S
03
co
QZ
O
Cs iH r-4 i*4 r-4
CQ
rH cn
Cu 54
XJ
3 CQ
CQ
CQ
*r4
. o. o
H 0)
H
O 1-4
*r4
1*4
w
>>
r-i eo
u
U
54
Cu
3
WI
a
CO r-(
o
03
0)
<U
XJ
Wa
3 CO
XJ XJ XJ
z z z zCQ
3 >
ve
cr -h
CQ CQ CQ
54 XJ
<U os ra
' 5j
44
cus <u > 0)
<u Cu
S3
S3 3 03
03 <M
i--4 a j-i
ffl UJ
3
3
3
z z z zO
o CQ O
c <s
o u
o
3
CO
CQ
CQ
S 03
h cn
cn cq cn
cn pi os OS
r*4 CM
i--4 i-4 ^4
--4 r4
CM
d *4 <u
o' \
33
> 00 O 1"4 o c 3= a 0) H
CO 03 <u a o 3-4 XJ cu u O U-i a. o G. 3c cn o -H r-4 Cu a) CQ H H 3 cn > C Q) CQ 5 03 Z
>> \ a
c o H XJ CQ N H i*4 xa
a. o
n o XJ o cQ 54 XJ
X 23
i
Czu
H
3 XJ CQ >. cn
u <u N rt ^4 H 03 CQ XJ cn
a> O >I-->
0) o r--4 CQ
u
O Pu
3 <U
z
> cQ o
00 a H - V4 o XJ H c
zo
4*43 cn o
fH <u 01 i-*4
cu
03 0)
54
3 3 CQ
Pi S 22
XJ
5
ui
fl X
o o ca
CJ XJ
XJ CQ
XJ /~s 3
r-4 <0 O O
CQ rs
t4
cn C xj 03
(U iH 03
<0 3 H
XJ > ca
CQ CU
03 <U 0)
a J W XJ
3 3 CQ
C9 03 r-4
0) *S<*
ca 1
<0
3 o
cn *4 A
w XJ
Q a4 O 54 W 4J CO
aj Pu
XJ CO XJ
(Q P** -r4 a)
ri
>
-r4 1 3 H > o cn
H f-4 03
f--4 E r-l (U ca O < a
O H cn 54
0)
> O o
54 (U <3 -U XJ 03 *H >* ca
o Z
o <3 -H XJ XJ
a > ca cq a)
3 OS
ca oa
Pu a* o <u r-4 xi Q) xj > (U O -H
XJ
CQ XJ
3 03 Q iH
03 3 W 03 <U Bu < a
<u
zU4 i 0) o ca r-4 0U 03
CQ CQ H <u XJ *n r-4 CQ <u <U 54 XJ C3
oo OU 0) 03
JO lu
a3a J0 hJ ou XJ
03 a CQ O H i-4 <U XJ CQ O 54 3 3 ai *o XJ Vj O 0) O W a <X4 CU
XJ
/ f= cn
O iU XJ o CQ U XJ
X ca co
<u
MM au ? ca
Eo O u-l lu c 04 CQ
00 ca u 0u o
54 03 a; cq > 05 oa uo <V Cu
OS Pu
03 r-4 ca CQ Ot 54 TJ
oE Cu CQ
i--4 & CQ z H O i4 G) F XJ JC 3 i- XJ i-4
TJ o o E o <J 1-4
u U4 03 iH <u a
Oa ai 3 *n Cu i4 o XJ 54 cn 54 Ou ao
XJ cu 23 <U U 4 a
o CQ
V
03
r-4
CQ
1-4
U
41
XJ
zCQ O H
Cu XJ
<u (Q XJ U
rH XJ
1-4 rH
(su H
Pu
41
rH ca
03 Oi CQ
r-4
i-4 4)
CQ >
> <
uO
a
a> M
31
Cu Cu
aO cn 44
003564
o Q -S
0a0s
cco\
CM
CaOs cCoT\
rt 0
.83 -o 0M0 --CI.
wg o U
ua xua> y o
<u XaI 3 >o z
>u. a 3
C
.ua0Uo1
a) y
O
C u rre n t S p e c ia l :o b le m a P ro je c ts
003565
O
-M
(0 y
u
u
m
oo. a.
33
V3
&.
H
sS3
O z
S3
S3 03
J* O
w
o<
8 aca
Cl
3-
O
c o
Ct4O
u
u
o
o. o
*
Ph
o
<U
oa3
C
PS
4J
n CO
U
CO CO
jCjO <uu H
H X0J) M
CO
Sos CoU
CO 0) S CO
CMJ ^OCO. >^
c o
00
00)0
CHJ poO 0) <
CtnO Oou *0H3 Q c(1o) T33 rC-O4
CELANESE CHEMICAL COMPANY Chemcel Plant Bishop, Texas
To: Dr. R. R. Graham From: G. D. Boyd
GDB-135-81
September 4, 1981
Laboratory Department Summary August, 1981
Chemical
J. J. Fritsch W. H. Brough J. B. Brown R. R. Carpenter M. W. Clifton R`. S. Hahn W. A. Heenan A. A. Miller B. C. Kerr C. W. Lee D. E. Lockwood A. G. McGehee W. H. Meyer D. G, Pausky 0. W. Schnellenberger G. R. Scholz D. D. Siemonsma W. L. Sharp K. R. Stelts H. H. Thigpen
Distribution
Plastics
R. G. Brandt A. C. Abshier R. L. Bunkley H. L. Davis D. A. Reck E. J. Heinz
CCCTC
G. J. Fisher W. E. Heinz W. T. McNair Central Files (2)
J. N. Gann, Bay City J. E. Sanborn, Bayport J. L. Paul, Clear Lake D. W. Harris, Pampa T. H. Golson, Dallas
003566
File No: 303.3 ,-r> in 0 1
11 I u -j I