Document XRgm6nEgejZLROGN461DaExGR
Statement of John L. Nelson Vice President-Manufacturing, B.F.Goodrich Chemical Company
Prepared For Presentation At Department of Labor Hearings On Vinyl Chloride, Occupational Exposure Standard
July 8, 1974
X am John L. Nelson, vice president-manufacturing of B.F.Goodrich Chemical Company, a Division of The B.F.Goodrich Company. Our headquarters are at 6100 Oak Tree Boulevard, Cleveland, Ohio 44131.
I received a B.S. in Chemical Engineering from the University of Wisconsin in 1939. My experience in the chemical industry covers a period of thirtyfive years, all of which has been with Goodrich, and most of which has been directly or indirectly connected with the production of vinyl chloride and polyvinyl chloride. X was located in our Louisville plant for nineteen years, during the last ten of which I served as plant manager.
Seated on this panel with me are all of the Goodrich representatives who participated in the presentation by The Society of the Plastics Industry, who will be available to answer questions on our testimony. They are:
- Mr. Anton Vittone President, B.F.Goodrich Chemical Company
- Mr. Philip J. Weaver Director of Industry Affairs, B.F.Goodrich Chemical Company
- Dr. Roger W. Strassburg Director of Environmental Affairs, The B.F.Goodrich Company
- Dr. Maurice N. Johnson Director of Environmental Health, The B.F.Goodrich Company
Also included on this panel is Dr. Condict Moore, Professor of Surgery and Director of the Cancer Center, University of Louisville School of Medicine. Dr. Moore will present a statement summarizing the program which the University is initiating pursuant to a grant from Goodrich.
The main purpose'of my testimony will be to examine the question of technical feasibility in the light of our current engineering and scientific knowledge. In addition, I will discuss on-going research and development programs directed at the reduction of vinyl chloride losses from our manufacturing operations. Our goal is to reduce vinyl chloride exposure to the lowest feasible levels and to preserve the jobs dependent upon this widely used and versatile plastic material.
We will discuss these subjects in terms of our own extensive experience. Specifically, we will review:
1, Vinyl chloride exposure levels in Goodrich plants.
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There are many variations within these types; solutions applicable to one type of process, product or plant are not necessarily applicable to other processes, products or plants.
The equipment used in the conversion of monomer to polymer in all three processes consists of multiple units of vessels, pumps, piping and valves, with thousands of potential sources of small fugitive or elusive Leakage of vinyl chloride gas. The process is batch-type and, after each reaction is completed, the vessel in which it is conducted requires varying kinds of purging, entering, cleaning, and preparation before the next batch can be started. These vessels, which we call polymerizers or reactors, have gone through an engineering evolution over the past thirty-five years.
During our first twenty years in the business, we used 1100-gallon reactors of stainless steel construction, which required entry and manual cleaning after every charge. This cleaning took about one hour, during which time workers cleaning vessels were exposed to vinyl chloride levels of an estimated 200-500 ppm. The worker would clean an average of five vessels every eight-hour work shift. We can only estimate early exposure levels, since the analytical sophistication to determine low levels of vinyl chloride in air has only been available in recent years. Our estimates were based on fragmentary data and interviews with employees to determine how often odor was evident, if and when they were aware of the intoxicating effect, and what level of explosimeter readings they might recall. While this method used to estimate exposure levels may seem crude by today's standards, our estimates are consistent with other similar testimony presented in this hearing.
Peak exposure levels ten and twenty years ago were one hundred times today's emergency standard, and probably averaged forty times today's average levels. My personal FVC experience goes back to when levels of exposure were of this magnitude.
Beginning in 1959, we experimented with glass-lined polymerizers and revisions to agitators and baffles to minimize buildup and cleaning time and did, as a result, reduce cleaning time to 20-30 minutes.
The next engineering breakthrough occurred in the late 1960's, with the Goodrich development of hydraulic reactor cleaning. This is a programmed high pressure water mechanism which is inserted into a polymerizer to renove buildup almost completely. This has greatly reduced human entry into polymerizers for manual cleaning. On some of our products, human entry has been reduced to as few as 3% of the batches. On some products, entry is still required after each batch. Over our total product mix, entry is required in about 10% of the batches.
Concurrent with the evolution of polymerizer design and mechanized cleaning, we installed additional equipment to improve the removal of vinyl chloride from the reactor prior to entry. With our current multi-step procedure, we have reduced vinyl chloride levels in open polymerizers down to the ambient level in the buildings today. The worker is further protected from vinyl chloride release from PVC resin buildup by use of an air line supplied respirator during the cleaning operation.
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Also included with this statement (EXHIBIT 3) is a six-months' history of area measurements of vinyl chloride levels by plants and by buildings showing the percentages of readings above 50 ppm and below 10 ppm.
This improvement is the result of aggressive and comprehensive programs carried out in each of our PVC plants and in our VCM plant to identify and correct Leaks, initiate operating improvements and emphasize increased employee communications. Here are some of the more important parts of these programs.
Leak Reduction
Leak reduction has been the single greatest source of reduced vinyl chloride levels. The indispensable key to this progress was diligent monitoring on a 24-hour a day, seven days per week basis to record concentrations of monomer and track down the exact source of each leak. Early in January, personnel were assigned in each plant to do nothing but measure and record monomer concentrations and identify sources of the concentrations. Then, corrective action followed swiftly. OVA monitoring is still being done to locate sources of leaks.
Now, continuous, recording fixed Bendix organic vapor analyzers are installed in all polymerization buildings in all plants. The Bendix instrument shows a higher reading if there is a significant leak anywhere in the area. The leak is tracked down with the portable OVA and repaired.
Operating Improvements
We have also made many operating improvements that have helped to reduce vinyl monomer concentrations in the work area. These include:
Vessels and pipelines containing monomer such as polymerizers, strainers, tank car unloading lines and Hamer blind installations, are being more thoroughly evacuated to recovery pumps before opening.
New procedures have been implemented for opening reactor manhole covers which reduce emission to the work area.
Regular vinyl monomer recovery operations have been improved and monomer efficiency raised.
Number of entries and time of each entry into polymerizer vessels for cleaning has been reduced.
Better manhole lid closure seals have been developed for polymerizers.
General ventilation has been greatly improved in many buildings. Localized ventilation has been installed at some repetitive trouble spots, such as pump seals.
Compressor and vacuum pump seal water have been put into closed systems.
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Although this new facility incorporates our latest technology, we fully expect to make additional improvements resulting from our on-going research and development work. It is expected that some of these improvements will take up to 24 months after the completion of the developmental effort.
Research and Development
Goodrich is doing everything it can with current technology, as rapidly as possible, to reduce vinyl chloride exposure levels. Further improvements and reductions in levels will come from the engineering changes and work practices we outlined previously. Improvements beyond these can only be achieved through future technological breakthroughs. In the past five months, we have redirected and greatly accelerated our research and develop ment efforts. We have 135 scientists and technicians at our Research and Development facilities and in our plants working on process and product improvements directed at lower vinyl chloride losses and reduced exposure. Our goal is to approach negligible losses of vinyl chloride from all sources.
About a quarter of the research and development effort is involved with analytical techniques and equipment, analyst training, and developmental analyses directed at worker exposure and residual monomer content of resins. During 1973, this effort resulted in selection of direct reading portable and sequential continuous monitoring equipment which have been essential tools in our efforts to reduce vinyl chloride levels in work areas of our production plants. Current effort is being directed toward more precise and rapid measurement of worker exposure.
About half of this research and development effort concerns fundamental process improvements to reduce losses inherent in our present processes. To our knowledge, there is no FVC production plant in the world operating in a completely closed polymerizer mode because of the buildup problem ` in reactors. Our programs toward this end include investigations of the fundamental mechanisms leading to resin adherence to polymerizer surfaces and a wide variety of methods aimed at eliminating adherence, chemically and/or mechanically. It is difficult to estimate how soon, if ever, we might achieve our goals in a practical way.
The balance of our research and development program includes reduction of monomer losses beyond the polymerization area. This is the development of a process by which the vinyl chloride monomer is removed from the PVC resin slurry before drying, thus increasing the recovery of vinyl chloride monomer.
This would also result in lower residual vinyl chloride in our finished resins when proven in production plant installations. We can foresee completion of this work and installation of facilities in two to four years for the majority of our resins.
Finally, in order to reach levels below .01% residual vinyl chloride in some PVC resins, we see the necessity for some basic changes in our manu facturing technology and the structure of PVC particles. This will take time to complete the small-scale work and scale up to production facilities.
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in vinyl chloride monomer and polyvinyl chloride plants, including reactor cleaning, where exposure is at low levels, regular work type clothes (coveralls or pants and shirts with full length sleeves) should be adequate.
Vinyl Chloride Level in PVC
Goodrich supports the SPI proposal that appropriate labeling of PVC con tainers be required when vinyl chloride levels in PVC exceeds 0.1%, effective October 5, 1974 and, further, that the requirement for labeling be changed to 0.017 effective October 5, 1977.
Labeling
We support the SPI position that the language to be used on signs at regulated areas emphasize the precautionary steps to be taken, rather than "scare" language emphasizing the nature of the substance.
Similarly, we support the SPI concept of product labeling, both monomer and polymer, and agree that such labeling should be designed to provide information to those who need it, rather than a basis upon which to panic because of a potential disease characterization.
As part of our overall effort, on Hay 1, 1974, Goodrich made a grant to the University of Louisville Medical School Cancer Center. This was the result of Goodrich's desire to bring continuing comprehensive medical advice and consultation to the situation and to support a broad scientific inquiry into the problem.
At this time, I present Dr. Condict Moore, Professor of Surgery at the University of Louisville School of Medicine, who will summarize the program which the University is initiating pursuant to a grant from Goodrich. Dr. Moore's statement is attached.
IN SUMMARY, then, Goodrich's position is as follows:
1* We are committed to reduce vinyl chloride exposure to the lowest level that is feasible through a combination of engineering changes, work practices, the part-time use of respiratory equipment, and technological development.
2. A no-detectable level of VCM in. its monomer and polymer plants is not technically feasible.
3. Full-time use of respiratory protection by PVC and VCM workers is not feasible.
4. We will be forced to shut down our PVC and VCM operations if the proposed
permanent standard is adopted.
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EXHIBIT 1 PLANT START-UP DATA AND ENROLLMENT
Plant and Location Avon Lake, Ohio Henry, Illinois Long Beach, Cal. Louisville, Ky. Pedricktown, N. J. Calvert City, Ky.
Total
Type of Product PVC PVC PVC PVC* PVC Monomer
Start-up Date 1953 1965 1960 1942 1970 1950
*Also vinyl chloride monomer until 1968
Current PVC or Monomer Enrollment
481 76
100 465 118 250
1,490
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EXHIBIT 2
PERSONNEL MONITORING DATA
A limited amount of data have been taken during May and June, 1974. The data for various operations have been categorized to show the number of values in several ranges of vinyl chloride concentration. All data are time weighted averages over a four-hour period absorbed on carbon tubes and tested by gas chromatography. This data does not, in all cases, represent actual worker exposure since every worker wears respiratory equipment when the work atmosphere is greater than 25 ppm or where operations and experience show there is a risk of exceeding 25 ppm.
OPERATION -- PVC POLYMERIZATION
Charge Operator
Recovery Operator
Hydraulic Reactor Cleaner Operator
Poly Cleaner
0-5 22 12
6 3
PPM VC1 Ranges
6-10
11-20
21-35
55
2
8 13
2 2. 32
0 1
Over 35 0 1
2 1
OPERATION -- MONOMER PRODUCTION
Furnace Operator VC1 Purification Operator Tank Farm Operator
0-5 2 7 0
PPM VC1 Ranges
6-10 11-20 21-35
110
00
0
2 12
Over 35 0 0 0
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EXHIBIT 3
VCL MONITORING DATA
Area Measurements Using Portable and Fixed Instrumentation, Measuring Total Hydrocarbons by the Flame Ionization Method
PLANT: AVON LAKE. OHIO
Building 451
Product
Dispersion Resin
461
Suspension Resin
464
Suspension Resin
463
PVC Latex
Month
January February March April May June
January February March April May June
J anuary February March April May June
January February March April May June
% Readings
Above 50 PPM
3.5 3.9 2.6 4.9 2.7 4.7
7 Readings
Under 10 PPM
8.7 14.4 23.4 42.9 65.2 72.5
4.7 3.3 2.5 3.4 2.2 4.9
24.1 37.9 21.7 14.6 59.3 57.8
5.1 3.1
1.1 0.0 2.8 2.8
11.1 10.3 34.8 58.9 71.2 82.5
0.0 0.2 0.0 0.7 0.4 1.9
70.9 91.7 97.5 97.6
86.3 82.3
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EXHIBIT 3 - Coat'd.
VCL MONITORING DATA
Ares Measurements Using Portable and Fixed Instrumentation, Measuring Total Hydrocarbons by the Flame Ionization Method
PLANT: HENRY. ILLINOIS
Building 731
Product
Suspension and Dispersion Resins
Month
January February March April May June
X Readings
Above 50 PPM
33.0 10.0
2.0 4.8 2.3 2.9
% Readings Under 10 PPM
20.3 17.4 27.9 69.1 82.0 79.1
PLANT: LONG BEACH. CALIFORNIA
Building
Product Suspension
Resin
---
Month
January February March April May June
X Readings
Above 50 PPM
2.6 1.8 2.4 2.2 0.5 1.3
% Readings Under 10 PPM
Data not analyzed
ii M
a
II If
M
It It tl II
II II
84.4
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EXHIBIT 3 - Cont'd. VCL MONITORING DATA
Area Measurements Using Portable and Fixed Instrumentation, Measuring Total Hydrocarbons by the Flame Ionization Method
PLANT: LOUISVILLE. KENTUCKY
Building 121
Product
Dispersion Resin and Latex
Month
January February March April May June
% Readings Above 50 PPM
10.9 3.2 0.6 1.7 1.0 0.9
% Readings Under 10 PF
0.2 5.9 40.8 62.0 86.2 88.3
111
Suspension
J anuary
Resin
February
March
April
May
June
9.1 2.0 1.5 1.8 L7 1.5
0.2 5.9 36.0 71.0 90.2 90.5
1
Suspension
January
Resin
February
March
April
May
June
15
Copolymers
January
Solution
February
Resin
March
April
May
June
115
VC1 Recovery
January
Purification
February
March
April
May
June
3.0 0.6 1.3 1.3 1.2 1.1
0.4 7.8 21.0 73.8 90.9 91.2
6.4 2.2 1.2 2.2 4.6 1.7
0.7 5.1 29.4 64.7 62.9 78.6
- Data Not Taken -
3.0
0.5
5.0
9.3
1.9 5.4
34.7 33.3
0.8 25.2
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EXHIBIT 3 - Cont'd.
VCL MONITORING DATA
Area Measurements Using Portable and Fixed Instrumentation, Measuring Total Hydrocarbons by the Flame Ionization Method
PLANT: PEDRICKTOWN, NEW JERSEY
Building 512
Product
Month
Mass Polymerization
January February March April May June
% Readings Above 50 PPM
5-1 2.0 1.1 0.6 1.4 0.6
% Readings
Under 10 PPM
35.7 46.5 69.3 76.2 79.3 80.7
513
Suspension and Dispersion Resins
J anuary February March April May June
3.8 2.4 1.0 0.7 1.2 0.5
39.1 66.0 81.3 78.8 75.2 75.9
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