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NATIONAL CONFERENCE . ON
POLYCHLORINATED BIPHENYLS
DAVID WOOD CHLORINATED BIPHENYL DIELECTRICS THEIR UTILITY AND POTENTIAL SUBSTITUTES
November 19 - 21, 1975 Pick - Congress Hotel Chicago, Illinois
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Monsanto
I DEPOSITION I EXHIBIT
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CHLORINATED BIPHENYL DIELECTRICS THEIR UTILITY AND POTENTIAL SUBSTITUTES
1. INTRODUCTION
In 1970, Monsanto voluntarily begsn its program of terminating sales of chlorinated biphenyls to open applications -- those which could result in losses to the environment. By late 1972, this program was fully implemented and Monsanto was'selling these products only to manufacturers of sealed electrical equipment such as transformers and capacitors.
Major applications affected by our withdrawal were carbon less paper, fire resistant hydraulic fluids, heat transfer t fluids, and plasticizers.
Sales for other miscellaneous minor applications were dis continued during the same period.
This action resulted in a reduction, in the use of chlori nated biphenyl, in areas where entry to the environment was less controllable, of some 45 million lbs. per year.
We decided at that time to continue supply to closed electrical applications because we believed that:
a) Entry of chlorinated biphenyl to the environment was
limited and controllable;
b) A more biodegradable, lower chlorinated homolog had
been developed which the capacitor industry could use;
c) Withdrawal would have brought to a halt production of
equipment essential to the safe and efficient distribution
and use of electrical energy because there was no known
satisfactory replacement for chlorinated biphenyl
dielectrics.
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Today wa continue to sail chlorinated biphenyl observing the following policy* 1. Wa supply only to manufacturers of sealed electrical
equipment such as capacitors and transformers. 2. Wa supply lower chlorinated homologs, Aroclor 1016,
to the capacitor industry. 3. Wa offer an incineration service for liquid PCB
wastes. 4. We continue to work with ANSI Committee C107 and
other bodies to establish appropriate handling and control procedures for equipment containing chlori nated biphenyl. 5. Wa allocated increased research resources in 1969
r to seek and develop affective replacements. This program continues. 6. In seeking possible replacements, we will ensure that differences between Aroclor and candidate fluids from our program are widely reviewed in order that the potential impact of any compromises is fully evaluated. The implementation of these and other programs both by ourselves and electrical equipment manufacturers was prompted by the utility of this dielectric family and the difficulties inherent in developing substitutes to effectively and fully replace it.
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II. UTILITY OF CHLORINATED BIPHEMYL IN CAPACTTOpc
1. Fire Resistance
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The adoption of chlorinated biphenyls in 1929 as capacitor dielectrics stemmed from their superior dielectric properties compared to mineral oil. However, recognition of the fire resistant character of the fluids influenced system and equipment design and standards over the subsequent 45 years. It is probably true that today many people find it difficult to assess potential capacitor fire hazard purely because Aroclor has been used for 45 years.
Particular examples where fire resistance in a capacitor is of benefit include!
a) fluorescent lighting ballasts; b) air-conditioner motor capacitors; c) television capacitors; d) large power capacitors where high fault currents
can cause rupture and ejection of fluid from pole mounted units close to people and buildings; e) industrial furnace capacitors.
2. Stabil ity
The persistence of chlorinated biphenyl in the environ ment is associated with the high degree of thermal, chemical, oxidative, and hydrolytic stability which permits capacitor manufacturers to supply to the exacting reliability requirements which exist today.
.3. Dielectric Constant/Dielectric Strengths
These properties are important in determining the size of a capacitor. In a mixed dielectric system, e.g., Paper/Aroclor or Paper/Polypropylene/Aroclor, the dielectric properties of Aroclor permit optimization of stress distribution between the components making up the dielectric layer.
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Thia has enabled capacitor manufacturers to reduce paper and film volumes for a given capacitance. I shall discuss- under the heading of "potential sub stitutes", the impact that this could have on: a) paper/film availability and usager b) design of equipment containing capscitors.
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III. UTILITY IK TRANSFORMERS
Chlorinated biphenyl transformers represent less than 15% of transformers in service. Their use is associated with the need to limit fire hazard in installations.
1. Railroad Transformers
Multiple unit cars as used in rapid transit systems have transformers mounted beneath each car. By nature of the type of service, involving high passen ger density, safety is essential.
2. Urban Power Substations (e.g., Underground Vaults)
These designs need to take account of city center space limitations and, also, the safety of the public and maintenance crews. Fire resistant liquid trans formers are helpful to all these objectives.
3. Industrial Load Centers
Efficient system designs for large, power intensive, manufacturing plants (e.g., automotive assembly, steel production) often incorporate transformers close to the electrical load centers. The use of Aroclor transformers at these centers, in the heart of the plants, or overhead in roof structures, protects both employees and plant.
4. Transformer/Rectifiers
Programs to reduce the emission of particulate matter from stack gases, for example in fossil fuel generating plants, include installation of electrostatic precipi tators. The transformer/rectifiers energizing the precipitator field must be located close to the cleetrodes. In many designs, the multiple transformers are located in a penthouse above the precipitator.
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A fir* in th* penthoua* could lead to cloa* down of th* precipitator and thua, th* generating plant, if pollution control ia to be maintained. A fire reaiatant fluid ia of obvioua benefit in thia application.
Zn each of thea* application, Aroclor protect* the
ayatem fromt
a) Initiation of a tranaformer fluid fire, by an electrical fault beneath the liquid level;
b) Electrical breakdown of the fluid cauaing emiaaion of flammable gaaea;
c) Propagation of fire if the tranaformer liquid content ia involved in an external fire.
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IV. POTENTIAL SUBSTITUTES IN CAPACITORS
Research Objectives
In seeking pctentisl substitutes, cur research objec tives, of necessity, related to those properties which gave Aroclor its value. Equally, we recognized the need that an Aroclor replacement should eliminate environmental concerns.
Desirably, a replacement should operate across the full range of current Aroclor capacitor applications while requiring minimum changes in design of capacitors and equipment utilizing capacitors.
The use of chlorinated biphenyl is worldwide. Monsanto manufactures chlorinated biphenyls both in America and Great Britain. We supply to the capacitor industry of many countries. We sought potential replacement products that could be made available with the consis tent quality control applied to Aroclor on a worldwide basis.
We referred earlier to availability of co-dielectric components in capacitors. A solution which required substantial changes in availability of polypropylene film (quantity or quality) or a major increase in short-term availability of capacitor paper, we con sidered unsatisfactory. If in 1974, such increased quantities had been required, they would not have been available. Capacitor production would have fallen short of demand, further jeopardizing efficient power supply.
Our research objectives can be broadly summarized in the following Table 1.
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TABLE 1
POTENTIAL SUBSTITUTES CAPACITORS
RESEARCH OBJECTIVES
1. MAT OR EXCEED AROCLOR 1016 CAPABILITY.
A) DIELECTRIC CONSTANT - USAGE OF OTHER COMPONENTS DIELECTRIC STRENGTH - CONVERTABILITY
B) STABILITY POWER FACTOR
- RELIABILITY
C) FIRE RESISTANCE
- SAFETY
c
2. GOOD ENVIRONMENTAL COMPATIBILITY.
3. A) SPAN EXISTING APPLICATIONS - COMPLETE SOLUTION. B) INTERNATIONALLY AVAILABLE - NOT SOLELY U.S.A. SITUATION.
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2. Non-PCB Candidate
The capacitor' industry is currently examining two Monsanto non-PCB (candidate) dielectrics. These contain no chlorinated biphenyl and are not chlori nated products.
The two fluids are designatedt
MCS 1238 MCS 1588.
Both of these products are blends of synthetic hydro carbons with a high dielectric constant additive to give a dielectric constant equivalent to Aroclor 1016.
Table 2, on the following page, lists some of the properties of MCS 1238 and MCS 1588 compared to Aroclor 1016.
Corona inception and extinction voltages are more a function of capacitor design than of the liquid, itself. Preliminary industry results demonstrate results in capacitors equivalent to Aroclor 1016. Further full scale work is required before final conclusions can be drawn.
Dielectric constants relate closely to those of
Acorlor 1016 over the temperature range of capacitor
operation.
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Hydrolysis stability is mentioned because of work carried out on earlier candidates based on esters which gave concern because of hydrolysis instability.
Hydrolysis was assessed by measuring the neutralization number of a sample with 0.5X water added, which had bean heated for 168 hours at 210*F. in a stainless steel bomb along with an aluminum and a mild steel coupon.
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3 Fire Resistance
Neither MCS 1238 or 1588 is fire resistant. This deficiency versus Aroclor 1016 trust be closely considered.
4. Environmental Considerations The environmental/health evaluation of capacitor replacement fluids must be related to: a) Degradation - If some quantity enters the environment, at what rata and through which mechanism will it degrade? b) Tissue Accumulation c) Toxicity - Occupational Safety Environmental Compatability
5. Degradation Biodegradation has been studied using a semi-continuous activated sludge technique. Forty-eight hour exposure of Aroclor 1254, Aroclor 1016, and MCS 1238 dielectric fluids to activated sludge using a semi-continuous procedure resulted in the following percent biodegra dation rates and 95% confidence limits:
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MATERIAL Aroclor 1254 Aroclor 1016 MCS 1238
TABLE 3 48 -HOUR S BIODEGRADATION
15 - 38 33 - 14 70 - 10
FEED CONCENTRATION.PPM 1 1 3
For the polychlorinated biphenyl (PCB) materials, the level of chlorination appears to be the most significant factor in their relative biodegradability. The rate of biodegradation decreases as the number of chlorine atoms per biphenyl molecule increases. Chromatograms representing samples after exposure to activated sludge show significant alteration in the Aroclor 1016 isomer distribution, but little for Aroclor 1254. Degradation of the non-halogenated fluid, MCS 1238, proceeds much more rapidly than for the halogenated PCB fluids with no evidence of resistant components.
Methodology for this technique is described in Appendix B.
6. Tissue Accumulation
Table 4 (Graph) depicts the results of Rat Tissue Residue Level Studies vs. Time and compares Aroclor 1242, Aroclor 1016, and MCS 1238 (see following page).
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c FAT TISSUE RESIDUE LEVEL VS. TIME
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25 PPM FEED LEVEL FOR RATS
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A fraction of the ingested Aroclor 1242 end Arocler 1016 was stored in rats' lipid reservoirs. However, most of this residue was depleted after the rats had bean on the basal laboratory diet for several weeks. During the course of the feeding study, residues of Aroclor 1016 accumulated more slowly and to a significantly lesser extent than those of Aroclor 1242. During the recovery period, these PCB residues decreased to lower values for Aroclor 1016.
The residue concentrations of MCS 123S quickly reached a stable level well below the concentration in the feed. The residues did not increase with continued exposure. After feeding of the treated chow was ceased, the MCS 1238 residues were rapidly metabolized and/or excreted.
The tissue residue accumulation and depuration profile of MCS 1238 shown in Table 4 is markedly different than those of the Aroclor fluids, especially that of Aroclor 1242.
Methodology is given in Appendix A.
Toxicity
Before samples of MCS 1238 could be evaluated in the
capacitor industry and within Monsanto, acute toxicity
data was gatheredi
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a) Rat - Acute single oral dose LDS0: 3800 mgAg.
b) Rabbit - Dermal LDjgi 5000-8000 mg/kg.
c) Rabbit - Potential eye irritation - A slight degree of irritation resulted when 0.1 ml. of undiluted MCS 1238 was placed in the conjuctival sac of the rabbit eye. The average maximum score recorded at one and again at twenty-four hours after treatment was 12.0 on a scale of 110.0. All eyes had regained normal appearance seventytwo hours after dosing.
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d) Rabbit - Potential akin irritation - Whan undiluted, MCS 1238 waa held in continuoua twenty-four hour contact with intact rabbit akin, a moderate degree of irritation reaulted. The maximum average acore waa 3.6 on a scale of 6.0.
Further programa are in proceaa, or acheduled, to atudy the following:
a) vapor Inhalation . b) Ultimate Degradation c) 90-Day Pilot Feeding Study d) Long-Term (2-Year) Feeding Studiea e) Fish Tiaaue Reaiduea.
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Concluaiona
To summarize Monsanto research activities!
- A large number of single compounds and mixtures have been evaluated in terms of physical property data, environmental compatability, fire resistance, and model capacitor life testing.
- These have led us to conclude that: a) Aroclor 1016 may well be sufficiently degradable to remain in controlled use. b) MCS 1238 is a potentially acceptable replacement with the qualification that it is not fire resistant.
- Further programa must be completed with MCS 1238 in order tot a) Deepen our knowledge of its environmental compati bility. b) Permit complete evaluation by the capacitor in dustry across their range of applications. c) Enable utilities, capacitor users, and agencies to evaluate the significance of decreased fire resistance.
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As a closing thought to this section, Z would life* to comment that sines 1929 whan Aroclor was first davaloped as a capacitor dielectric, norral commercial pressures havs spurred efforts to find supperior replacements. The awareness of environmental accumulation of chlorinated biphenyls from other applications added further impetus for more intensive research in the chemical and electrical industries. Aroclor has defied 45 years of search for a superior replacement.
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V. SUBSTITUTE TRANSFORMER FLUIDS
Neither Monainto nor any other company, to our knowledge, haa developed a transformer dielectric with equivalent fire reaiatanee to that of Aroclor. The diffieultica that we face in common with other workera in thia field are two-foldi 1. Aroclor haa become the reference atandard for fire
reaiatanee in tranaformera becauae it worka and haa worked for 45 yeara. To eatabliah atandarda to guide research effort, there ia a need for objective evalua tion of the fire hazard aaaociated with the major aectora of tranaformer uae. 2, The chemiatry which imparta fire reaiatanee tenda also to produce stable molecules. Monsanto seeks replacement products that will provide protection against; a) Fire from tranaformer faults under the liquid surface; b) Fire from secondary ignition of gaseous arc de
composition products; c) Fire propagation if the transformer is involved
in an externally initiated conflagration. We strive to accomplish this and produce an environ mentally compatible product. We have four candidates which are currently being evaluated by the tranaformer industry. These materials are in a suffi ciently early stage of development that it would be premature to give detailed property data at this meeting.
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APPENDIX A
Methodology For Feeding Study
Feeding end Sampling
Ret chow containing 25 ppm Aroelor 1242, Aroelor 1016, or MCS 1238 waa prepared by mixing the products into Ralston Purina rat chow. The treated chow was fad ad libitum to adult albino rats for an exposure period of 30 days. Following the 30-day exposure period, all re maining rats were placed on the basal laboratory diet. At predetermined intervals during the exposure and re covery periods, five rats from each exposed set and a control set were sacrificed. Fat tissue was excised for analysis and composited for each group. Samples were quick-frozen and stored in glass containers with aluminum foil-lined caps to minimize risk of contamination.
Iaolation
The dielectric fluid residues were isolated from the fat by solvent extraction. A weighed amount of fat was placed in an Erlenmeyer flask and homogenized three times with 25 ml of pesticide grade hexanes and anhydrous sodium sulfate using an ultrasonic homogenizer. The combined supernatants and washings were filtered through anhydrous sodium sulfate and diluted to 100 ml with hexane.
Lipid Weight Determination
A 5 ml aliquot of the extract solution was pipetted into a tared 50 ml beaker. After evaporation of the solvent under a stream of nitrogen, the beaker and residue were reweighed to obtain the lipid weight of.the aliquot. All residue levels are reported as ppm on a lipid weight basis.
PCB Clean-Up And Measurement
Sample clean-up for the extracts containing Aroelor 1242 and Aroelor 1016 residues was accomplished by pipetting an aliquot of the extract onto a 5% deactivated alumina column and eluting with 125 ml of hexanes. The column eluate was collected in a Kuderna-Danish evaporative concentrator, a
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3-ball Snyder condenser wee attached, and the solution was concentrated xo 5 ml. The residue levels in the extracts were measured by gas chromatography using an electron capture detector.
Non-PCS Clean-Up And Measurement
Sample clean-up for the extracts containing MCS 123S residues required separation of the residues from the lipid by preparative scale gel permeation chromatography. Following the GPC separation, the extracts were further cleaned up on an alumina column, collected, and concentrated as above. The residue levels in these extracts were measured by gas chromatography using a flame ionization detector.
Calculations
Calibration curves for each product were prepared by plotting detector response (total peak area) versus nanograms of standard injected. Residue levels in the samples were determined by summation of the total area of peaks corresponding to peaks in the standard and use of the appropriate calibration curve. The calculations were done as followsi
(N)(VF) Residua(ppm) ----------------
(Vj)(W),
where N amount of product from calibration curve (ng) V volume of final concentrate (ml) F Vj volume injected (ul) W lipid weight of original sample (g).
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APPENDIX B
Biodegradation Method
Sine* activated aludga it ona of tha most important agents for aawaga treatment, tast proeaduras avaluating its action ara of graat importanca.
Tha semi-continuous activatad sludga (SCAS) mathod has baan axtansivaly utilizad in tha davalopmant of biodagradabla datargants. In our SCAS procedure, pattarnad aftar tha Soap and Datargants Associations standard mathod (1,2,) mixad liquor (activatad sludga and suparnatant) from a local domastic sawaga treatment plant is chargad to magnetJcally-stirrad glass vassals of 1.5 litar capacity. Haans for aeration and sampling ara provided. The SCAS unit is generally operated using a retention or aeration time cycle of 24 to 72 hours. At tha beginning of aach eycla, synthetic sewage (300 mg glucose, 200 mg nutrient broth, and 130 mg K2HPO4) and the appropriate test material in ethanol solution ara added to tha mixed liquor (2500 mg/ litar suspended solids concantration). Aeration is main tained until tha end of tha cycla, at which time the sludga is settled and ona litar of supernatant drained. Tha cycla is than re-initiated by the addition of tap water, synthetic sewage, and tast material. Operation of tha units can ba continued for an indefinite period of time until consistent degradation rates ara observed.
Sample Analysis
Biodegradation of tha test material was determined during one cycla each week by analyzing 20 to 50 ml mixed liquor samples withdrawn after feeding and at tha and of the aeration cycle. Tha mixad liquor analytical procedure involved extraction with three successive 25 ml portions of hexane, and drying combined extracts with anhydrous sodium sulfate. Extracts wars concentrated in a KudernaDanish evaporative concentrator equipped with a 3-ball
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Snyder condenser, end measured by electron, capture, or flame ionization, gas chromstography. calibration curves for each product were prepared by plotting detector res ponse (total peak area) versus nanogrars of standard injected.
The percent biodegradation vss calculated from the following equations % Biodegradation (Ce - Cn)/C0 x 100 where CQ and Cn use the initial and final concentration of test material, respectively, on the mixed liquor.
References
.
1. J. Am. Oil Chen. Soc. 4, 9G6 (1965).
2. J. Am. Oil Chem. Soc. 46. 432 (1969).
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