Document EdLYJGOB832k4Q16yKVyRg2n0

THE PROPER HANDLING OF AROCLORS AND THEIR MIXTURES IN THE ELECTRICAL INDUSTRY Monsanto u Monsanto Chemical Co. Organic Div. Sales Dept. 800 N. Twelfth Blvd. St. Louis, Mo. = . G. GEN I GNu 5 '.'AY 1, 1955 01442*4 TOWOLDMONOQ22984 01 TOWOLDMONOQ22985 INDEX Introduction Chapter 1 Chapter 2 Chapter 3 Chapter 4 Chapter 5 Chapter 6 Chapter 7 Chapter 3 Chapter 9 The Proper Handling of the Aroolora and Their Mixtures In the Electrical Industry. Procedure for Unloading Tankcars of Aroclors and Their Mixtures. A. Description of the Cars. B. Procedure for Unloading the Cars. C. Drum Packaging Storage Tanks A. General Description of Storage Tanks. B. Detailed Description of Storage Tanks. Gasketing and Pump Packing. Sampling. Laboratory Analysis and Procedure for Treating Aroclors and Their Mixtures. Test Procedures. Typical Properties. Earth Treatment of Aroclors and Their Mixtures in the Electrical Industry Prior to Use. Dermatology and Toxicology. Attachments: Drawing No. 31-20848, Dome Detail. Drawing No. 31-20847, The Tank Car. Drawing No. 90-8170-5, The Horizontal Storage Tank. Drawing No. D-13362, The Vertical Storage Tank. Drawing No. 90-8248, The Breather. Drawing No. 90-8278, The Varec Gauge. Drawing No. 90-8178, The Unloading Platform. 0144266 TOWOLDMONOQ22986 THE PROPER HANDLING OP AROCLORS* AND THEIR MIXTURES IN THE ELECTRICAL INDUSTRY INTRODUCTION Monsanto's Aroclors*, especially the chlorinated biphenyls including types 1242, 1248, 1254 and 1260, used alone or in combination with chlorinated benzenes, are commonly used die lectric materials of the Askarel^ class. Askarel is a generic name referring to liquid dielectrics derivadlcfiro* halogenated aromatic hydrocarbons possessing excellent chemical and dieleotrie stability and fire-resistance over the temperature ranges and operating conditions required of transformers and capacitors in the electrical industry. The properties of Aroclors and their mixtures, used as dielectrics are described in detail in Chhpter 7 entitled, "Typical Properties". These dielectrics are manufactured under very carefully controlled conditions in order to meet the striot and exacting electrical requirements and properties. The electrical industry's use of these fluids has been largely in accordance with the General Electric Company's patents and developments. Aroclors - Monsanto's chlorinated blphenylB and ohlorinated polyphenyls. Registered U.S. Patent Office. 1F. M. Clark, "Electrical Insulation", Chem. Eng. News 25, 2977 (1947). 1 01 V>267 TOWOLDMONOQ22987 Resulting from the wide use of these materials In the Industry, trade names have been established to Identify them by different manufacturers of electrical equipment. Listed alphabetically the trade nameB Include, "Chlorextol," Allis Chalmers; "Dlaclor," Sangamo Electric; "Dykanol," Cornell Dublller; "Elemex," Line Materials; "Hyvol," Aerovox; "Inerteen," Westlnghouse Electric; "NOflamol," Wagner Electric; and "Pyranol," General Electric Company. The purpose of this bulletin Is to asslBt the Industry With'theoproper and safe handling of these dleleotrlc materials In their operations. 2 0144268 TOWOLDMONOQ22988 CHAPTER 1 PROCEDURE FOR UNLOADING TANKCARS OF AROCLORS AND AROCLOR MIXTURES A, Description of the gars Aroclor and mixtures of Aroclors with chlorinated benzenes are shipped by Monsanto In two types of Insulated tankcars both of which are either aluminum lined or zinc-tin metallized. One type of aar has heating colls Inside of the tank and these are In direct contact with the product. The other, a more widely used type of car. Is a double-shell tank with heating colls between the Inner and outer shells. The steam coll connections are at the bottom of the car. Both types of tankcars are tested for 60 pounds pressure and their steam colls are tested for 200 pounds gauge pressure. The cars are top-unloaded by displacement with dry air containing 10 mg. HgO/cu. ft. maximum. There are two or three connections on the tankoar dome depending on the type of car. Where three connections exist, one Is a two Inch diameter unloading line which extends to the bottom of the car, the second Is a one Inch diameter air Inlet connection and the third Is a two Inch diameter pressure safety vent, which Is a thin lead disc adjusted to release any pressure In excess of 60 pounds gange. This safety vent is hooded for protection against dust, dirt or accidental bumping. Where only two connections exist on the dome, one is the two Inch diameter unloading line and the other is the safety 3 TOWOLDMONOQ22989 vent. On these cars, it is necessary to remove the safety vent and introduce the displacement air through that connection. Drawing No, 31-20848 shows in detail the dome of a tankcar with three connections. "A" is the two inch unloading line which extends to a Bmall Bump at the bottom of the car. "B" is the one inch air inlet connection. "C" is the hooded safety vent. The car dome oover with fitted bolts is shown in the center. It is fitted with a Garlock 901 asbestos gasket or an ^.Aluminum envelope Goetze gasket. This drawing also shows a bottom opening in the car. ThiB can be opened only from the inside of the car and its purpose is for cleaning operations. It has no use at all in unloading the oar. Drawing No. 31-20847 shows the over-all dimensions of the 8,000gallon Aroclor tankcar. B. Procedure for Unloading the Cars The car should be spotted at an unloading dock similar to the one shown by Drawing No. 90-8178. The car must be level and the brakes set properly. "STOP-Tankcar Connected" signs should be placed fore and aft the car to warn switching crews. If it is raining or snowing or the humidity is extremely high, it is not advisable to open the car. In case the car must be sampled and opened during bad weather, a canvas canopy must be placed over the dome of the car. It is preferable to unload the cars under roof or inside the factory. Unless it is absolutely necessary because of following described situations 4 01i*270 TOWOLDMONOQ22990 the dome oover should not be opened until ready for sampling. The dome cover is sealed with a standard railroad wire and seal, and Monsanto should be notified If this seal Is foundbbroken upon receipt of the car. The first step In unloading Is to Inspect the dome and clean around the dome oover to remove all loose dirt, water or snow. Wiping rags and a brush should be used to clean before the dome cover and connections are opened. Then, the screwed hood over the alr-inlet valve should be removed and this valve opened fully and left open while heating the car. A Weston or metal encased thermometer should be in serted through this alr-lnlet valve opening and the temperature of the interior of the oar determined. If the car temperature Is below the caution temperature shown in the following Table 1, It will be necessary to take the special step of Inserting a "halr-pln" heating coll through the dome of the car to preclude rupturing the tankcar seams during the heating period. Product ASTM Pour Point C. Temperature00C. Below which Caution Must Used in Heating Aroclor 1260 Aroclor 1254 Aroolor 1248 Aroclor 1242 Pyranol 1467 + 30 + 10 -7 - 19 Pre-heating + 40 ii 20 +5 - 10 is not required* Pyranol 1470 Pre-heating Is not required* Pyranol l48l Pre-heating is not required* Except if the material has cooled below -10C. and crystals of scavenger have separated. Then, the material should be heated to 70C. (158F.) until complete solu tion has been accomplished. 0H<|771 TOWOLDMONOQ22991 If the dome of the car Is to be ppened for the pre-heating operation, it is necessary that it be covered with a clean canvas. Extreme care must be taken to avoid getting dirt or moisture into the car. It is due to the relatively h$h viscosity of some of the Aroclors at low temperatures that it becomes necessary to form a column of molten material from top to bottom of the car, in the center, to prevent hydraulic pressure build-up which may rupture the tank shell if there is too rapid localized heating when employing the main steam ooils. When such pre-heating is required, a satisfactory vent hole can be made by inserting a "hair-pin" coil (l/*} inch diameter brass, galvanized, or stainless steel pipe) into the open dome of the oar and introducing steam through the coil until there is a column of fluid Aroclor from top to bottom. After the vent hole Is melted through the material to the bottom of the oar, the "hair-pin" coil should be removed and the dome cover replaced and bolted. Steam is then introduced into the main coils. It is recommended that the steam pressure be limited to 100 pounds gauge pressure, particularly in the case where the coils are In direct contact with the Aroclor. The steam coil outlet should be trapped or throttled with a valve. It will require eight to twenty hours to bring the material to pumping temperature - depending upon weather 6 0144272 TOWOLDMONOQ22992 conditions. It is essential that the air inlet valve be open during the heating period in order to vent the tank. Some calculations have been made to indicate the heat requirements for an Aroclor car. Data for an 8,000 gallon car of Aroclor 1254 are: Specific Gravity = 1.5 Specific Heat = 0.26 BTU/lb./F. Heat requirement for heating Aroclor from 30C. (86F.) to 110C. (230P.) is: 8000 x 1.5 x 8.33 x 0.26 x (230-86) 3,774,000 BTU. For heating from 30C. (86P.) to only 75C. (167P.), the heat required is 2,110,000 BTU. A nine horse power boiler operating at 80 pslg produces 263 lbs./hr. of steam with no reused oondensate. Returning oondensate at 200F. will increase the steam output to 296 lbs./ hr. at 80 psig. In the first case, heating to 110C., the over-all heat transfer co-efficient is assumed to be too low to utilize the IOO56 capacity of the boiler. A value of 1500 for UA with an average ^ T of l44P. indicates that the useable steam is 202,000 BTU/hr. or 226 lbs./hr. steam at 80 pslg. In the second case the ^ T is lower and the entire output of the boiler is useable. Table II sumB up the approximate time calculated to heat Aroclor 1254. 7 0144273 TOWOLDMONOQ22993 TABLE II Nine HP Boiler Lbs. Steam/Hr. 30-110C. 30-75C. 100# cap.(no reused condensate) 75# cap.(no reused condensate) 100# cap.(condensate @ 200F.) 75# cap.(condensate @ 200F.) 263 -- 296 -- -- 9 Hrs. 18 hrs.(86#cap) 12 Hrs. -- 8 Hrs. 18 hrs.(76#cap) 11 Hrs. Calculations on a five horse power boiler give heating times of the following order: Five HP Boiler Lbs.Steam/Hr. 30-110C. 30-75C. 100# cap.(no reused condensate) 146 28 hrs. 16 hrs. 100# cap.(condensate @ 200F.) 164 25 hrs. i4 hrs. Aroclor cars can be heated by steam (80-100 psig) to the proper handling temperatures in a reasonable time by using a boiler source capable of producing 200,000 to 300,000 BTU/hr. The times given here are approximate and will act as a guide until experience shows the exact time for this operation. 8 TOWOLDMONOQ22994 The proper handling temperature for the various fluids is given in the following Table III, which indicates cor responding viscosity values: TABLE III Product Handling and Pumping Temperature C Approximate Viscosity, ! Aroclor 1260 Aroclor 1254 Aroclor 1248 95 - 130 75 - HO 50 - 85 100 - 43 100 - 42 100 - 40 Aroclor 1242 Pyranol l48l 35 - 75 30 - 75 100 - 40 100 - 40 Pyranol 1467 20 - 55* 100 - 40 Pyranol 1470 15 - 45* 100 - 40 *If any of the scavenger is out of solution, then the material must be heated at 70C. (158 F.) until it has dissolved. Selection of pumping temperatures for any dielectric not Bhown on this list or which may be developed in the future should be based on a viscosity of about 100 Saybolt Universal Seconds for average pumping and about 40 S.U.S, for fast pumping. When the material has been heated to pumping temperature, a one-half Inch diameter pipe "cross" arrangement containing a pressure gauge, air inlet, pressure relief valve to relieve at 30 PSIQ, and vent connections, should be connected to the dome air inlet pipe. Shen the unloading line should be connected. 9 TOWOLDMONOQ22995 (At this point a sample is taken as described in Chapter 4,) Dry* air is then introduced Into the tankcar and pressure built up to 15 pounds gauge. The two inch valve cock on the Btand pipe is opened and the discharge pipe observed to be sure the liquid is being uftloaded. To protect the seams in the tankcar, the pressure must not exceed 30 pounds. The car will begin to unload at about 12 pounds pressure. When the oar is empty, the air pressure will drop off rapidly and air will blow out of the vent on the receiving tank. The air flow may be stopped at this point and the tankcar pres sure released through the vent valve on the ."cross" arrange ment. After Inspecting the car to be sure that it has been completely unloaded, all connections and dome cover should be closed tightly. It is essential that the empty tankcar be sealed immediately after the oar is unloaded in order to keep the car filled with dry air during return shipment. As a final *It is essential that the displacement air used for unloading be dried thoroughly by some dehumidifying unit such as soda lime, activated alumina or similar dehydrating agent drying unit. It may be necessary to recharge the dehumidifying unit each time that a car is unloaded. For unloading a tankcar of ArocHar within three hours, 15 standard cubic feet a minute of air at 15 pounds per square inch gauge pressure 'afifla -10P, dew point should be supplied. If the dry air unit is to be used only for unloading tank- cars, a small single tower dryer unit containing a self-contained reactivating heater is suggested. Two manufacturers of air dryers of this type are: C. M. Kemp Mfg. Co., 405 E. Oliver Street, Baltimore 2, Maryland and Pittsburgh Lectrodryer Corporation, Foot of 32nd Street, Pittsburgh, Pennsylvania. . 10 014^76 TOWOLDMONOQ22996 step, it Is desired that a standard railroad wire seal be in serted through the slotted bolts of the car fittings. Steam should be released from the car coils and all condensate re moved from the colls by blowing with air with the steam trap by passed. All connections must be replaced as received. Adequate care should be taken in preparing and sealing the oar for return shipment. Unloading with dry air as described is the preferred and recommended procedure because it is done with the car dome closed which avoids contamination. If the car is unloaded by pumping out of the top, which required opening the dome. It is most desirable that the car be Bet inside of a building. If this cannot be done, then, a canopy or roof should be provided over the oar dome, and the unloading should be done when the weather is clear. A centrifugal pump with minimum capacity of 40 gpm. is suggested. It will be necessary to prime the pump and only clean Askarel should be used to do this. Another method for priming the pump is to use a Penberthy steam Jet, No. 22A available from Penberthy Injector Co., 1242 Holden Ave., Detroit 2, Michigan. If a flexible unloading line lavaed, it Bhould be a flexible metallic hose. Rubber hose must not be used. 11 014*276.01 TOWOLDMONOQ22997 C. Drum Packaging ' Drum packaging la made with new and carefully Inspected 55-gallon drums. These steel drums are lined with a specially selected baked phenolic coating. An example is NESCO No. 3 lining offered by the National Enameling and Stamping Company, Long Island, New York. Contents of the drums should not be heated by direct application of flame or strip heaters. Radiant heat from steam colls or hot air in a heated room Is to be pre ferred. The screw plug In the drum head is fitted with a metal cap as a safe guard against tampering. 12 TOWOLDMONOQ22998 CHAPTER 2 STORAGE TANKS A. General Description The storage tanks should be a minimum of 10,000 gallons and preferably 12,000 to 15,000 gallons capacity to accommodate the normal 8,000 gallon tankeara. It is preferable to locate the tanks above ground where they are easily accessible for any changes or repairs. Under ground location presents difficulty in this respect. Especially In cold climates. It Is preferable to locate the tanks Inside of a building. The tanks should be located conveniently with reference to the tankcar unloading facilities and the area where the dielectric Is used. Although Aroclors are non-oorroslve to metals, corrosion or rusting of Iron and steel equipment (by oxidation) may occur resulting In contamination of the products. The resis tance of Aroclors to materials of construction Is given In Monsanto Technical Bulletion O-P-115, entitled, "The Aroclors," Page 6, Stainless steel tanks are very satisfactory but relatively expensive. Stainless steel pipe Is relatively difficult to fabricate and It Is difficult to make tight leak-proof connec tions. Storage tanks may be of steel construction If properly metallized with zinc-tin or aluminum on the interior surfaces 13 01*<.27B TOWOLDMONOQ22999 coming in contact with the AroclorB. The metallizing should be done according to the following procedure: 1. Clean an area of the surface by sand blasting, or a similar method, to give a perfectly clean and roughened surface. The area cleaned should not be greater than can be completely metallized within a few hourB after cleaning. 2. If zinc-tin metallizing is used, a coating of zinc 0.005 inches thick should be sprayed on to the cleaned surface. This is followed immediately by a coating of tin 0,007 Inches thick. 3. Aluminum metallized surfacing should be about 0.01 Inch thick. The detailed procedure for metallizing and oleaning is outlined as follows: a) Sand blast, b) Coat with iron, 0.005 inches thick. (The purpose of this coating is to provide a rougher and better bond for the finish coat of aluminum or the zinc-tin combination.) o) Apply the selected finish coat, d) Pill the tank with tap water and warm it with steam, (if an open steam line is used, do not allow the steam to impinge directly onto the metallized surface of the tank.) e) Drain the tank, f) Fill with cold water and drain, g) Wipe dry with clean diaper cloth or other fabric relatively free of lint, h) Heat the tank to at least 100C. (212P.) to expell moist air. It would be beneficial to heat the tank, allow it to cool and pull dry air through it using a dehumidifying breather in the air line, heat again etc. until the tank is-full of comparatively dry air. 1) Spray about 100 gallons of new, electrical grade Aroclor (not high 14 0H4279 TOWOLDMON0023QOO in viscosity) or electrical grade trichlorobenzene onto the inner walls of the tank, washing the walls thoroughly (avoid breathing any fumes), j) Attach the circulating pump, the lines used, and the filter press fitted with dry paper and cir culate the fluid through the system and the tank. Install new dry filter paper several times in the presB during this dry ing and cleaning operation. Discard the dielectric fluid used for cleaning, k) Partially fill the tank with new Aroclor dielectric and analyze it electrically and chemically to de termine whether it meets specifications. If all tests are met, then fill the tank with the dielectric. The tanks should be insulated using, preferably^ glass foam beads as supplied by Dow-Corning or Libby-Owens-Pord. The suggested thickness of the glass Insulation is one inch mini mum to two inches maximum. The glass insulation may be covered with tar material commonly used for weatherproofing. Another type of insulation which may be used instead of the glass is 8556 Magnesia-Wool which should be covered also with the weather proofing tar. The advantage of the glass insulation is that it is not moisture sensitive as is the case with Magnesia-Wool. If the Btorage tank is located outdoors, it is best that the insulation be covered with riveted or bolted tin sheeting painted with aluminum paint. This type of metal surface weathers well and is cleaned easily. All piping must be gal vanized and screwed fittings must be back brazed to assure TOWQLDMON0023001 tightness. All handling pipe lines must be traced with steam lines and Insulation applied over the ttyo lines In order to keep the handling lines and the material up to the desired pumping temperature. Usually a one-fourth Inch copper steam line running parallel with the handling line will suffice. Under very severe conditions of low temperatures. It would be desirable to wind the steam line around the handling line about two turns to the foot. The tanks must be provided with ample pressurized heating coll surface to supply sufficient heat to the material to bring It to the proper temperature for pumping and handling as Indi cated In Table III, Heating colls should be either metallized steel, or preferably steel coils which have been galvanized after fabrication. It Is recommended that the steam pressure on all heating colls should not exceed 100 pounds per square Inch gauge; lower pressures may be used where practicable. It is essential that all steam colls be completely free from even minute leaks since this will introduce water into the product. The steam colls may be Introduced as "hair-pin" colls through a manhole at the side and bottom of the tank, or as Is most often done. Inserted through the manhole at the top of the tankrand then located near the bottom. External heating oolls located in the Jacket of the tank may be used but this construction Is more expensive and less efficient than the internal coils. 16 TOWOLDMON0023002 The storage tanks may be fitted with a stirrer, either through the top, side, or bottom of the tank and the propeller blade should be located near the bottom of the tank. However, insertion of a stirrer through the side offers possible source of a leak and since these materials are homogeneous, it is not essential to provide such agitation for the purpose of mixing. Adequate circulation can also be accomplished by using a centrifugal type pump. Gear pumps or other equipment where wear or chipping of metal parts may introduce contamination should not be used. The pumps must be of the type designed to handle hot oil. All wetted pump parts should be either stainless steel or bronze. The centrifugal pumps must be provided with a deep stuffing box and proper packing used, as described in Chapter 3. As examples of pumps found com pletely satisfactory for this service, reference is made to Worthington Worthite pumps. Blackmer pumps, and Dayton Dowd Type C pumps for handling hot oil. Also, a very satisfactory arrangement for mixing or circulating and pumping the fluid from the storage tank is to use a vertical sump pump such as a Taber pump. All storage tanks must be amply provided with a dehumldlfying breather such as soda lime, activated Alumina, etc., units. This is essential to prevent moist air from coming in contact with the dielectric. A moisture content above 35 ppm 17 TOWOLDMON0023003 adversely affects the electrical resistivity of these pro ducts. Provision should be made to preclude possible leakage dC the drier material back Into the storage tank and the drier should be Inspected periodically to make sure that It Is open and not plugged. B. Detailed Description Drawing No. 9C-8170 shows the detailed construction of a horizontal 15,000 gallon storage tank for Aroclor and Its mixtures which bias been found completely satisfactory. The various nozzles on this tank are used as follows, con sidering them In order from left to right on the drawing: 3" nozzle 24" nozzle Inlet for recirculation For future agitator If required (not used) 3" nozzle For soda lime or calcium ohlorlde breather connection 36" manhole For Inspection, etc. The float gauge Is located In the center of this manhole. 3" nozzle 24" nozzle Not used. For future agitator If required (not used) 3" nozzle Not used 3" nozzle Filling Inlet connection 18" X 26" Oval Nozzle For sump pump 3" nozzle For thermometer well (see detail) The two 24" nozzles were originally Installed for Installa tion of agitators. If required. However, It has been found 18 TOWOLDMONOQ23004 unnecessary to use agitators In the storage tanks, and these nozzles could be omitted. It has been found that circulation of the fluid by the sump pump, and into the nozzle at the opposite end of the tank, for several hours gives satisfactory blending of the tank contents. For pumping the dielectric from the storage tank, a "Taber Pump Co. all bronze 2-1/2" X 2" vertical sump pump with monel shaft has been found to be quite satslfactory for the applica tion. The liquid level gauge used in the storage must be gastight. The storage tanks are equipped with Vapor Recovery Systems Co.'s "Varec," gas-tight, automatic tank gauge as shown by Drawing No. 9C-8278. The storage tanks should be provided with an operating plat form suitable to the customer's conditions of operation. The dehumidifying units used as breathers on the storage tanks can be constructed as shown by Drawing No. 9C-8248. The upper portion of the chamber is charged with anhydrous soda lime or another drying agent. Periodic inspection of the drying agent will show the formation of a cake of damp material on top about 1 to 1-1/2 inches deep. This cake should be removed and fresh material recharged. Any suitable con struction similar to that Bhown on Drawing No. 9C-8248 may be used for the breather units. Drawing No. D-13362 shows design detail of a 15,000 gallon TOWOLDMON0023005 vertical storage tank. The vertical type tank would seem especially desirable when insufficient space is available to accommodate the horizontal type tank. 20 01**285 TOWOLDMON0023006 CHAPTER 3 GASKETING AND PUMP PACKING Aroelors and their mixtures soften and swell natural rubber and many of the synthetic "rubber" materials. Such material not recommended for use. Include Hycar P, Koroseal, Perbunan, Neoprene, etc. These materials are known sources of contami nation. Suggested types of packing and gasketing materials include: 1. For Welded Flanged Pipe Connections: Garlock Packing Co., No. 901 or No. 7021, 1/8 Inch asbestos fiber sheet. A ring of thin aluminum drawn tightly at the flange connections may be used satisfactorily also. 2. For Pumps: Oarlock No. 234, No. 431, and Cheveron No. 705O-C are satisfactory packings. Likewise, Durametallic'8 spiral asbestos fiber may be used. Johns-Manvllle and others have comparable packing materials. 3. For Valves: Oarlock No. 117 braided packing or its equivalent is suggested. 4. Other Resistant Materials: It is Indicated that duPont's Teflon, poly tetrafluoroethylene is not attacked by hot (I30c.) Aroclor and is to be recom mended as a gasket material. Dow-Corning's Silastic, Silicone 180, is very resistant to Aroclor and is suggested for gasket purposes. 5. In some cases cork impregnated under pressure with Chrysler's Cycloweld 55-9 or Armstrong Cork Co.'s 1162-J and oured at 170C. may be used as a gasket material. These are baked phenolic type coatings. 6. Pipe Thread Compounds: When necessary to use pipe thread compounds, the following Bhould be satisfac tory if care is taken to prevent the pipe compound from getting on the inside of the pipe. (a) Plastic Lead Seal--manufactured by Durametallic Corp. (b) Ordinary white lead . 21 014*2 bfe TOWOLDMONOQ23007 Usually It Is not necessary to use pipe thread com pounds since all screwed pipe fittings should be sealed by back brazing. 7. All new lines and fittings should be cleaned thoroughly by steaming (for two hours) and dried with air or heat. 22 01<t*287 TOWOLDMON0023008 CHAPTER 4 SAMPLING METHODS 1.) The ASTM Standard Method for sampling electrical insulating oils is described in ASTM Designation: D923-49. This describee glass and metal thiefs for sampling drums, cans, and tankcars. A specially designed thief or bomb for sampling tankcars is described, also. A very good instrument of this type is the stainless-steel Baoon Bomb Thief with which samples of the liquid can be drawn from any level of the tankoar. The ASTM procedure describes sample containers, their cleaning and storage. Under general precautions,.the ASTM mentions that, "Samples of the fluid Bhall not be taken until the oil is at least as warm as the surrounding air, because cold oil may condense enough moisture from a humid atmosphere to affect seriously its insulation properties, (in the case of tankcar lots, on some occasions there may be no choice, as it may be necessary to procure samples from a tankcar when the temperature is not above the surrounding air. On such occasions, the temperature of oil and air, also the humidity if possible, should be noted in the report of test results.) It is unde sirable to do any sampling when the relative humidity of the atmosphere exceeds 75 percent, and samples shall never be taken in the rain." 23 TOWOLDMON0023009 At the plants of several electrical manufacturers using Aroclor dielectrics, the practice is to switch the tankcars directly into the plant building or under roof before sampling and unloading. These precautions in handling are taken to avoid any contamination of the fluids which are manufactured under very strict specifications. For example, the specification for ionizable chlorides allows no more than 0.10 parts per million. Moisture may not exceed 30 to 35 parts per million. Tankcars are cleaned and prepared under close Inspection before they are filled. When filled, and analysis shows the material in the car to be satisfactory, the car is then sealed with a standard railroad wire and seal Inserted through the slots of the dome fittings. Likewise, after the tankcars have been unloaded in the industry, it is requested that the done fittings should be sealed with a railroad wire and seal. 2.) Monsanto Methods used for sampling tankcars differ somewhat from the ASTM procedure. The modified techniques are used because of their greater simplicity and they have been entirely satisfactory as employed over many years. A sample is never taken when it is raining or snowing or when there is any chance of contaminated atmosphere moving in the direction of the car. However, in oase of an emergency, during inclement weather, a canopy is placed over the car dome before sampling. 24 OH`,289 TOWOLDMONOQ23010 A satisfactory Bample bottle is a five pint, round amber glass, packer type container fitted with a 38 millimeter Bake- lite sorew cap with an aluminum or tin cup liner. Bottles of this description can be purchased from the Northwestern Bottle Company, 3lM North Broadway, St. Louis, Missouri according to their No. A-7253. Only new bottles and oaps are used. When a shipment of bottles is received, the bottles are oapped immediately and stored in their receiving oartons. Prior to use, the exterior of the bottles is wiped with a clean cloth. The simplest sampling devloe used is a clean stainless steel or aluminum dipper. However, this is not a generally preferred device because it permits sampling the oar from the near surfaoe, only. The sampling devloe commonly used consists of a stainless steel tube, seven feet long with one end bent into a hook, to serve as a handle and on the other end there is a stainless steel bucket with a perforated bottom. This bucket is about 5-1/^ inches inBide diameter and 6 inoheB deep to hold the five pint bottle. This bottle is held firmly by a stainless steel oollar made to slide along the shaft of the sampling devloe. This collar has a clamp attachment for fixing it tightly into place where desired around the neck of the bottle. When a car is to be sampled, a new sample bottle is clamped firmly in the bucket. All dirt is brushed and wiped away from the car dome area using a clean rag. . -25- TOWOLDMONOQ23011 The oar dome is opened and the cap is then removed from the sample bottle. The sampling device Is Inserted Into the car so that the neck of the bottle is at least twelve to eighteen inches below the surface of the fluid. The sample taken is dis carded as its purpose is to rinse the bottle, A portion of the sample is used to rinse the interior of the bottle cap. This procedure is repeated until a minimum of three rinses has been made; each time the sample-taken is not put back into the car. These rinses should be discarded. Then the sample is taken and the oap of the bottle is screwed down tightly. When the sample has been obtained, the car dome is.replaced, immediately. The exterior of the cample bottle is wiped with a clean cloth and when returned to the laboratory it is further clean ed with a cloth dampened with pure trichlorobenzene. If the sample is to be shipped, the cap is taped with Scotch Tape. The sampling device is also cleaned with pure trichloro benzene and is stored in a dust free, air conditioned.>room. 3.) Drum Sampling. A glass thief, thoroughly cleaned with pure trichlorobenzene and dried is used to sample drums. 26 TOWOLDMONOQ23012 CHAPTER 5 LABORATORY ANALYSIS AND PROCEDURE FOR TREATING AROCLORS AND THEIR MIXTURES WITH EARTH A sample of the Aroclor or Aroolor mixture taken from the tankoar, or drums, as described in Chapter 4, is analyzed in the laboratory to determine its quality in accordance with the property values given in Chapter 7. For capacitor use, usually the Important properties tested are resistivity, power factor, chlorides, and moisture. For transformer use dielectric strength, resistivity, moisture, and ohlorides are the important properties. If the sample is out of line with the shipping specifica tions, it is indicated that the sample has become contaminated. In this case, another sample is to be taken and the properties redetermined. If still out of specifications, the sample should be given treatment with earth. Treatment of the dielectric with conditioned Attapulgus earth will bring the electrical properties to the maximum attainable values. While there is complete agreement on the benefits derived from treating with conditioned earth, there is difference of opinion on details of the method, arising from factors such as the following. No doubt, there are differences in the absorbent power of various types of dlatomaceous earth with respect to removing moisture, impurities and additives such as stabilizers or scavengers from the dielectric 27 OV*'*292 TOWOLDMONOQ23013 materials. The size of the earth particles, temperature and conditions of activation of the earth, the concentrations used and the temperature, the degree of agitation and time Interval at which the dielectric 1b given earth treatment are all possible variables which are still being studied In various laboratories. The method used by Monsanto for treating the fluid with activated earth In the laboratory is: The absorbent is minus 200 mesh Attapulgus* earth ac tivated Just prior to use by heating in shallow trays for four hours at 400C. (752P.) or for at least twelve hours at 250C. (482P.). At least one quart of the dielectric sample Is placed Into a clean two liter Pyrex beaker or three necked flask. The beaker or flask should be cleaned Just prior to use In a manner similar to the procedure described In Chapter 6, Method No. 11,751 "Procedure for Cleaning of Electrodes, O.E. Cell and Accessories". The flask or beaker Is fitted with a glass or stainless steel agitator. Heat is applied using either a hot plate or a Qlas-Col mantle and is controlled by a thermostat such as a Fenwal thermo switch with a stainless steel sheath. About 0.1 to 0.2# of the activated earth, based on the weight^of the liquid is added. Attapulgus Division, Minerals & Chemicals Corp. of America, 210 West Washington Square, Philadelphia 5 Pennsylvania 28 01491 TOWOLDMONOQ23014 The more viscous dielectrics such as Aroclors 1248 and 1254 are heated at about 70 to 80C. (158 - 176F.) and the less viscous materials such as Aroclor 1242 and Pyranols 1481, 1467, and 1470 are heated at about 50 to 60 C. (122 to 140F.). After heating and stirring the sample for about four hourB, it is filtered using a clean Pyrex glass suction flask and a buehner funnel fitted with a Whatman No. 1 or No. 3 filter paper. This apparatus and the bottle into which the treated sample of dielectric is transferred should have been cleaned in a manner similar to the cleaning procedure de scribed in Chapter 6. The earth treated and "up-graded" sample is then ready for final analysis of its electrical properties. 29 01*9299 TOWOLDMONOQ23015 CHAPTER 6 TEST PROCEDURES A. general Information The Monsanto test methods described here with the special equipment used are some of the control tests employed to main tain the quality of Aroclors for dielectric use. They are suggested as a guide for test work needed to indicate the quality of the dielectrics used in the manufacture of electrical goods. The most significant electrical tests made on Aroclors for capacitors are: 1. Dielectric constant. 2. Power Factor. 3. Resistivity. For transformer use the most significant tests of Aroclor mixtures are: 1. Dielectric Strength. Si Resistivity. In both cases a significant chemical test is corrosion chlorides. The following terms are defined: Dielectric Constant: The dielectric constant (sometimes called specific induc tive capacity) of any substance is equal to the ratio of the capacitance of a condenser when that substance is used as the 30 014*295 TOWOLDMONOQ23016 dielectric to the oapacltance when there Is a vacuum between the conductors (for all practical purposes air at ordinary pressures may be used instead of a vacuum}. Dielectric Strength; Dielectric Strength is the rupturing strength of an Insulating material when subjected to voltage stress under specific conditions and expressed in kilovolts. Breakdown varies with the shape of the Electrodes and does not Increase directly In proportion to the thlokness of the dielectric. Power Factor; The power factor of a dielectric is the ratio of the ener gy loss in the dielectric to the "apparent power" in the di electric . Resistivity: Resistivity is electrical resistance offered to the pas sage of a steady current. The volume resistivity in ohmscentimeter of an oil 1b the ratio of the d-c potential gradient in volts per centimeter paralleling the current flow within the sample, to the current density in amperes per square centimeter at a given instant of time and under prescribed conditions. Volume resistivity is expressed in ohm-cm. The analytical procedures described in detail include: 1. METHOD NO. 11,751, "PROCEDURE FOR CLEANING OF ELECTRODES, G.E. CELS AND ACCESSORIES." 2. METHOD NO. 11,608, "DIELECTRIC CONSTANT AND POWER FACTOR." 31 TOWOLDMONOQ23017 3. METHOD NO. 11,605, "DIELECTRIC STRENGTH." 4. METHOD NO. 11,607, "RESISTIVITY." 5. METHOD NO. 10,126, "CORROSION AND CHEMICAL STABILITY." 6. METHOD NO. 10,118, "INORGANIC CHLORIDES." 7. METHOD NO. 10,087, "ACID NUMBER." 8. METHOD (MODIFIED) NO. 10,620, "MOISTURE (WATER)." Detailed Instruction and Testing Methods. 1. METHOD NO. 11,751, "PROCEDURE FOR CLEANING OF ELEC TRODES, G.E. Cell and Accessories. a. The Electrode Cleaning Procedure: 1) Place the electrodes in hot electrical grade Trichlorobenzene for ten minutes. 2) Wash with unheated TCB. 3) Rinse twice with methanol and twice with tap water, 4) Place the electrodes in hot 10# Tri Sodium Phosphate solution. Soak and heat for ten minutes. 5) Wash thoroughly wlth'tap water. CAUTION: After Step 5-- DO NOT TOUCH THE ELECTRODES WITH HANDS! 6) Wash with distilled water twice. 7) Dry in drying oven for at least two hours at 120C. b. The G.E. Cell Cleaning: 1) Reclean the dell before use, when more than 8 hours have elapsed since the previous cleaning. 2) Follow the procedure for the electrodes starting at Step 4. 32 01**297 TOWOLDMONOQ23018 0. Cleaning of the Accessories: 1) Apply the same cleaning procedure as given for the electrodes (Steps 1 to 7) to prepare the glass spacer and beaker for next test. 2) Clean the thermometer in the same manner as the electrodes, except for Step 7. 3) Place the wet thermometer (after Step 6) directly in position in the temperature Heating Unit (Modified Fisher Isotemp Oven) and allow to dry. 2. METHOD NO. 11,608. "DIELECTRIC CONSTANT AND POWER FACTOR." 1. Apparatus A. Oscilloscope: Heathkit Model 0-6. B. Constant Temperature Heating Unit: Fisher Isotemp oven. Model 13-245A, modified to include inter wall connectors. C. A. C. Generator: General Radio type 1302-A. D. Amplifier and Null Detector: General Radio type 1231-B with type 1261-A power supply. E. Capacitance Bridge: General Radio Co. Capacitance Bridge type 716-C. F. Test Cells: G.E. type, concentric cylinder electrodes Catalog #1,559663. G. Class B driver transformer: This is used for 60 cycle measurements to excite the bridge directly from the domestic power line. It has 50 volts output with a 4800 ohm resistor in service. H. Tuned Circuit Filters: General Radio Type 1231-P2 (400 and 1000 cycle) and 1231-P3 (60 cycle). These filters aid in obtaining a more accurate frequency for the measurements by removing harmonics, noise, hum, etc. 33 014429B TOWOLDMONOQ23019 II Adjustment of Controls on Electrical Apparatus A. On Panel No. 1 (Top Panel, Amplifier and Null Detector) a. Turn the 4-way (main power) switch on the upper right hand side to the #3 position to determine the Dielectric Constant at 1000 cycles. Turn this switch to the #2 position for measurements & bo cycles. b. Allow the equipment to warm up 10 minutes. c. Turn "GAIN CONTROL" to 6. d. Depress "INPUT 0.03V." button. B. On Panel No. g (Oscilloscope) a. Turn "INTEN." to about the 12 o'clock position. CAUTION: Do not allow a high intensity spot to remain stationary on the screen for any length of time. b. Using "HOR. POSITION" and "VERT. POSITION" controls center the Image on the screen. c. Adjust "FOCUS" for sharp line. d. Turn "FREQ. SELECTOR" to LOOKC. e. Turn "FREQ. VERNIER" to 80. f. Turn "VERTICAL GAIN" to 5. g. Turn "VERTICAL INPUT" fcO "10 VOLT MAX.". h. Turn "HORIZONTAL GAIN" to about 20. I. Turn "SYNCHRONIZING" to + 20. J. Turn "SYN." to "EXT. SYN." k. Turn "GEN." to "SWEEP GEN." 34 0144Z99 TOWOLDMONOQ23020 C. On Panel Ho. 3 (Capacitance Bridge) a. Turn "RANOE SELECTOR" switch to "100 C" for 60 cycle measurements and to "1 Kc" for 1000 cycle measurements. b. Turn "METHOD SWITCH" to direct. c. Turn "DISSIPATION FACTOR" selector switch to "0". D. On Panel No. 4 (oscillator) a. Disregard this panel for measurements at 60 cycles. b. On 1000 cycle measurements, depress the No. 10 "MULTIPLY BY" button. fl. Set "FREQUENCY DIAL" to 100. d. Turn "OUTPUT" dial so that pointer is at the end of the arrow. e. Depress the "UNBAL. 5000 OHMS" button. When all of the above adjustments are made, the electrical apparatus Is ready for measurement of Dielectric Constant and Power Factor. III. Determination of Constants for the Apparatus 1. Carefully assemble the oell which has been cleaned and dried within the last 8 hours. Refer to Method No. 11,751 for the procedure to use In cleaning the cells. 2. Place the cell assembly In the Fisher oven which has been adjusted to 25C. 3. Connect the back wire Inside the oven to the lead on the Inner cylinder of the cell and the front wire to the lead on the outer cylinder of the cell. 35 01*4300 I TOWOLDMONOQ23021 4. Connect the cable from the capacitance bridge to the terminals on top of the oven bo that the inner wire of the cable goes to the back terminal and tne outside mesh casing of the cable (the ground) goes to the front terminal. 5. Remove the thermometer from the top of the oven before going on with the testi TETs~Ib important. 6. Make all adjustments on the electrical apparatus ad directed in Part I of this method. 7. Balance the bridge by rotating the "CAPACITANCE" and "DISSIPATION FACTOR" dials on Panel NO. 3 until the wide vertical band on the oscilliBcope is adjusted to a minimum width. 8. Record the Bum of the readings on the "CAPACITANCE" dial and vernier and oall this value A. 9. Remove the beaker containing the cell from the oven and fill it with C.P. benzene .to a level O.737 inches (ca.3/4 inch) above the top of the concentric cylinders of the cell. 10. Adjust the temperature of the benzene to 25C. while stirring with a thermometer. 11. Replace the cell in the oven (at 25C.) and make the same electrical connections as in Steps 3 and 4. DO NOT interchange connections. 12.. Balance the bridge again as in Step 7. 13. Record the sum of the readings on the "CAPACITANCE" dial and vernier and call this value B. 14. Calculate the cell constant by the following equation: Cell Constant, K B - A (this is usually 2.2? a 1.0 around 70 mmfd.) 15. Remove the cell from the oven and balanoe the bridge as in Step 7 with the "CAPACITANCE" and "DISSIPATION" "FACTOR" dials. 36 0144301 TOWOLDMONOQ23022 16. Record the sum of the readings on the "CAPACITANCE" dial and vernier..and call this value F. (capacitance of connecting cable.) ~ 17. Calculate the CELL LEAD CAPACITANCE by the following equation: CELL LEAD CAPACITANCE, 0 . A - F - K (this Is "-- usually around 3 mmfd.) WHERE: A = CAPACITANCE OF ENTIRE SYSTEM IN AIR (SYSTEM CONSTANT) 0 CAPACITANCE OF THE CELL LEADS (CELL LEAD CONSTANT) P - CAPACITANCE OF CABLE AND WIRES WHICH CONNECT THE CELL AND CELL LEADS TO THE BRIDGE. (CONNECTOR CONSTANT) K - CAPACITANCE OF THE CELL ALONE (THE CELL CONSTANT) Tabulate the system Constant (A), the Cell Lead Con stant (G), the Connector Constant (F), and the Cell Constant (K) on a piece of stiff paper and post them near the Instrument where they can be easilyrreferred to for comparison and calculations. These constants must be checked at least once every three months and In all cases where the Dielectric Constant and/or Power Factor are out of specification. Measurement of Dielectric Constant and Power Factor on Ardclors, Pyranols, tnerteens, and Trl-Tetrachlorobenzene Blends. A. Test Run on Cell to Determine whether It Is Clean and Properly Aligned. ' 1. Carefully assemble a cell which has been cleaned and dried within the past 8 hours. 36 a 01**302 TOWOLDMONOQ23023 NOTE: Refer to method No. 11,751 for procedure to use in cleaning cells. 2. Adjust the oven oontrol to hold at a temperature of 100C. for all materials except Tri-Tetra Blends. If a Tri-Tetra blend is to be tested, adjust the oven to hold a temperature of 25c. 3. Place the empty cell assembly in the oven and connect the back wire inside the oven to the lead on the inner cylinder of the cell, and connect the other (front) wire to the lead on the outer cylinder. 4. Connect the cables from the capacitance bridge to the terminals on top of the oven so that the inner wire of the cable goes to the back terminal and the outside metal casing (ground)goes to the front terminal. 5. Allow 15 minutes for the cell to reach temperature equilibrium Inside the oven. 6. Remove the thermometer from the top of the oven Before taking any measurements on the bridge. This Is Important. 7. Make all the adjustments on the electrical apparatus as directed in Part I of this method. 8. Balance the bridge by rotating the "CAPACITANCE" and "DISSIPATION FACTOR" dials on Panel No. 3 until the wide vertical band on the oscilloscope screen is adjusted to a minimum width. 9. Record the Bum of the readings on the "CAPACITANCE" dial and vernier and compare this value with the SYSTEM CONSTANT determined in Part II of this method. IMPORTANT: If the value obtained in Step 9 does not agree with the System Constant A (Part II) within 5 uuf, the cell must be re-cleaned, re-dried, re-assembled, and the test run for the System Constant must be repeated. NOTE: Although the above test run must be made prior to each analysis, the value obtained in Step 9 is not to be used in calculations but is to be used only as iPcheck on the cleanliness and alignment of the cell. 37 0H<i303 TOWOLDMONOQ23024 B. Procedure for Testing Materials 10. Remove the cell from the oven and fill the beaker with the material to be tested to a level 0.737 Inches (ca 3/4 Inch) above the cylinders of the cell. 11. Adjust the temperature of the sample to 100C. (use hot plate) for all materials except Trl-Tetra blends. For Trl-Tetra blends, adjust the tempera ture of the sample to 25C. using an Ice-water bath If necessary. NOTE: Stir sample continuously with a thermometer while adjusting the temperature. 12. Place the cell and sample In the oven and make the same connections from the cell to the bridge as In Steps 3 and 4. DO NOT Interchange connections. 13. Allow fifteen minutes for the cell to reach tempera ture equilibrium Inside the oven. 14. Remove thermometer from the oven before taking a measurement. This Is important? 15. Make the adjustment of controls on the electrical apparatus as directed In Part I of this method. 16. Balance the bridge by rotating the "CAPACITANCE" and "DISSIPATION FACTOR" dials on Panel No. 3 until the wide vertical band on the oscilloscope screen Is adjusted to a minimum width. 17. Reoord the sum of the readings on the "CAPACITANCE" dial and vernier, and call this value X. 18. Record the sum of the readings on the "DISSIPATION FACTOR" dial and switch. Call this value D. Calculations: Dielectric Constant X-F -0 ------- K------- Where: X - Capacitance reading from Step 17. F = Connector Constant (Determined In Part II) 0 -Cell Lead Constant (Determined in Part II) K - Cell Constant (Determined in Part II) 38 01**130* TOWOLDMONOQ23025 When assembling this booklet, a mistake was noted in the num bering of the pages. No page of contents is missing. Only number 39 was skipped. We are pleased to Insert number 39 as a blank page for your conveni ence for notes, if you care to make any. 39 0144305 TOWOLDMONOQ23026 # Power Factor f x D ~^b Where: f Test Frequency (60 cycles or 1000 cycles) f0- Frequency of "Range Selector" on Panel No. 3 D Dissipation Factor reading from Step 18. NOTE: When D (dissipation factor) Is less than 0.1, the dissipation and power factors differ by less than 0.0005. Therefore, for our measurements, power factors and dissipation factors are equal. Precision: (Reference: General Radio Manual for Model 716-C Capacitance Bridge) a. Capacitance readings are precise to i 2 mmfd. x mul tiplier reading ( 0.2# of full Beale for each range) when the dissipation factor Is less than 0.01. b. Dissipation Factor (Power Factor) readings are pre cise to i 0.0005 or J 2# of the dial reading which ever Is larger, for values less than 0.1 for D (Dissipation Factor). METHOD NO. 11,605, "DIELECTRIC STRENGTH." a. Apparatus and General Information The electrical equipment necessary to provide high voltage to permit the determination of dielectric strength of liquid dielectric at commercial power frequencies is basically quite simple. The equipment assembled in the laboratory consists of a high voltage transformer of good design and with a current capacity of 2.43 KVA and with equip ment for control Of the voltage and a means of measuring the voltage and to provide safety for the operator. 40 014*306 TOWOLDMONOQ23027 It is enclosed In a steel gray crackle finished cabinet measuring 42* high, 22" wide, 17" deep and set on truck casters for easy mobility. Protective equipment incorporated in this apparatus prevents the application of high voltage unless all safeguards are complied with. The door on rear of cabinet must be closed. The cover over the oil must be all the way down and the voltage control must be at 0 position, Failure to comply with these requirements will prevent any action when the red button is depressed. The test cup;. Transformers, Voltmeters, and Accessories The askarel testing cup type No. 224809 supplied by General Electric Company is mounted on the top rear of the oabinet. It is protected by a heavy plastic cover, hinged at the rear for accessibility to the receptical. It is equipped with safety contactor so placed that the circuit energizing the high voltage contactor cannot be completed unless the protective cover is completely lowered and in place. It is Impossible for the operator or anyone else to touch the testing cup when high voltage is applied. 41 01<i4307 TOWOLDMONOQ23028 The High Voltage Transformer manufactured by the Kelly-Koett Manufacturing Co. is of the closed core, oil immersed, shell type design. Rated @ 81,000 volt @ 40 millampers. It was recovered from a used X-ray machine, purchased quite inexpensively. An auto transformer from the same X-fcay machine is connected so aB to limit the out-put voltage of the high voltage secondary to 50,000 volts. The primary of the auto transformer is connected to the secondary of a 2-1/2 KVA powerstat variable auto transformer supplied by the Superior Electric Company. Power to the powerstat is controlled by a 4 con tact 30 amp. solenoid circuit breaker. The voltmeter mounted on top near front edge is connected across the powerst&t secondary and is calibrated to read directly in Kilovolts in the range of 0 - 50 K.V. The overload circuit breaker consists of a small relay connected between one side of the high voltage transformer secondary center tap and 42 01**308 TOWOLDMONOQ23029 ground. It is adjusted to break contact on a current drain of about 50 mllliampers. The circuit for the coll of the solenoid circuit breaker Is wired through the contacts of this relay. Safety and Operating Controls 1) Door Interlook switch located on rear door. 2) Test cup cover Interlock switch. 3) Powerstat switch mounted on rear of unit arranged so that high voltage contactor cannot be closed unless powerstat 1b at zero position. 4) Main power switch on front panel 5) Powerstat voltage oontrol on front panel. 6) High voltage contactor push button on front panel (red). 7) Signal lamps mounted on top around voltmeter. Purpose and operation described in method of use. Procedure 1) Ascertain that the temperature of the material under test Is 25 ( 0.5)C. NOTE; Testing at other temperature is likely to give variable results which may be misleading. 2) Shake the sample container so as to thoroughly mix the askarel before filling the test cup. NOTE: This operation is especially important with used Aroclor as the impurities may settle to the bottom and the test may be misleading. 3) Rinse the testing cup three times with small portions of the sample to be tested. 43 014<i309 TOWOLDMON0023030 4) Immediately after final rinse, fill the cup to a height of not less than 20 mm, (0.787 in.) above the top of the electrodes. 5) Rock the cup a few times in order that any entrapped air may escape. Close cover over oil test cup. 6) Allow to stand 3 minutes, CAUTION: THIS IS IMPORTANT. 7) Turn main toggle BWitch on front panel to "ON" (or up) position. Both green and amber pilot lights on the top at either side of the voltmeter will now glow. NOTE: The green signal light is connected across the 115 volt in-put and denotes that line voltage has been applied to operating control circuit. Amber light is connected in series with sensitive switch located under high voltage contactors and connected to its armature. It indicates that high voltage contactor is in its rest position and away from oontacts energizing auto transformer. 8) Turn voltage control (large knob on front) to extreme counter-clockwise position. 9) Depress red button on front. This energizes high voltage transformer and circuit breaker and is indicated by amber light going out and the red light directly over voltmeter will ligh^ 10) Watch the voltmeter and, while holding the button "IN", turn the voltage control at such Bpeed that will cause voltage as indicated on'voltmeter to 'rise at a fate of 3 K.V. per second. 11) Note and Record the voltmeter reading at breakdown. 44 0144310 TOWOLDMONOQ23031 12) Repeat the test until two successive break downs occur on each of two fillings of the test cup which do not differ by more than 10#. Report the average value of these two readings (Step 12) as the Dielectric Strength. If the limit of the Instrument Is reached before breakdown, report the Dielectric Strength as 50 K.V. at 25C. Cleaning of the test cup: After the test is completed, drain the cup. Plush the cup with benzene. Then fill with Aroolor 1248 and let stand, until the next analysis. NOTE: An exception, when samples of oil from the plant are brought In for test, the cup must be thoroughly cleaned with benzene and carbon tetrachloride before and after running the test. The electrodes: The testing cup has two electrodes. Both electrodes are movable and have twenty threads to the Inch with index notches on both the electrodes and the lock nuts. To set the Gap: Arrange one of the electrodes and the lock nuts with the Index marks In line. Move the other elec trode until It comes In firm contact with the first electrode and lock It. 45 0144311 TOWOLDMONOQ23032 Now unscrew the electrode with the Index marks in line (Step 1) two complete turns and lock it. This will leave a gap of 0.1 inch between faces of the electrodes. Cleaning of the electrodes and the test cup free of carbon coating: The following ASTM method of cleaning shall be followed when it is apparent from visual inspec tion that the electrode discs of the cup are coated with carbon. Wipe clean with dry calendered tissue paper the electrodes and the test cup. CAPTION: It is important to avoid touching the electrodes with the finger or with portion of the tissue paper whioh has been in contact with hands. Rinse the electrodes and cup with dry lead-free gaso line, StoddaaS Solvent (or dry, waterwhite Kerosene) until they are entirely clean. Care Bhould be taken not to touch the electrodes or the inside of the cup after cleaning so as to avoid possible contamination. 46 01`><i312 TOWOLDMONOQ23033 4. METHOD NO. 11,607, "RESISTIVITY." a. Apparatus: General Radio Company Megohm Bridge Type 544-B. This is a combination of Wheatstone bridge and vacuum tube voltmeter for indicating null. The direct measurement of resistance up to 1,000,000 megohms is made possible by the use of a vacuum tube detector which absorbs negligible amount of power. The voltage applied to the unknown resistor is held approximately constant, regardless of the value of the unknown resistance. This condition is necessary to measure resistance properly. The accuracy of the Instrument in the range en countered in the measurement of Aroclor resis tivity, 100 to 1000 megohm is i 6#. The instrument is equipped with a 115 volt AC power supply which supplies all operating voltages for the bridge Indicating circuits and in addition supplies 500 V DC for application to the material under test. The instrument is completely enclosed in a waxed finish shielded oak cabinet measuring 8-1/2" wide, 22-1/2" long and 8" high. Approximate weight--26 pounds. 47 01<K313 TOWOLDMONOQ23034 Test Electrodes: Two concentric nickel cylinders with feet, obtained from General Electric Company. The inner electrode has outside diameter of 2.8" and a height of 3.25" with area of 184 sq. cm. The outer electrode has an inside diameter of 3" and a height of 3.25" with area of 198 sq. cm. The distance between electrodes is, therefore, 0.1" or 0.25*1 cm. By theory, electrode constant (K) area/length is 191/0.25*1 or 752 where average area is 191 sq. cm. Also K 36 x 10" x C (farads with air as dielectric) or 11.29 x C (mmfd. with air as dielectric). Glass Plate: Pyrex about 3-1/2" diameter with concentric grooves to assist in spacing electrodes. Obtained from General Electric Company. Heating Unit: Assembled in the laboratory and is the same unit described in Dielectric Constant Apparatus (see Method No. 11,608; Equipment). Procedure: 1) Assemble the test cell. Place the recently cleaned (within the last 8 hours--see Method No. 11,751, Step 9) electrodes in an 800 ml. beaker. 48 on'*31'1 TOWOLDMONOQ23035 2)Measure the capacitance of the test cell (Cc) according to Method No. 11,608 (Dielectric Constant and Power Factor measurements.) 3) Fill the cell assembly until the liquid level Is 3/4 inch above the top of the electrodes. 4) Heat the assembly on the hot plate to 100 ( 0.5)C. 5) Place the assembly Inside of the testing oven. 6) Attach top lead (+) on the megohm bridge to inner electrode. 7) Attach other lead to outer eleotrode. 8) Throw the three switches at the top of the megohm bridge to "ON" position. 9) Allow 10 minutes for assembly to reach temperature equilibrium inside the oven. DANGER: Make sure control knob is in "CHECK" position. Otherwise, painful shock will result if leads are touched. c 10) Bring the galvanometer pointer to zero by turn ing the "ZERO ADJUST" knob in the direction in which the pointer of the galvanometer should move. 11) Turn the control knob to "CHARGE" position for 30 seconds. 12) Turn the control knob to "OPERATE" position and return the galvanometer pointer to zero by ad justment of the "MULTIPLY BY" switch and the megohm dial. 13) Read after 30 seconds. Calculation: Resistivity* - Megohm dial reading (Step 12) x "Multiply By" reading (Step 11) x capacitance of cell (Step 2) in mmfd. x 11.29 x 0.001. 49 ( U315 TOWOLDMONOQ23036 Report the result In units of 109 ohm-cm. Values of resistivity are qualified by designation of temperature and voltage. These are for this test, 100C and 500 volts DC. NOTE: It Is Important that the produot under test, electrodes, and beaker be at uniform temperature for this determination. Temperature variations In different parts of the sample will cause the galva nometer zero to change constantly and give misleading results. CAPTION; Inasmuch as measurements must be made at a potential of 500 volts DC a shock hazard exists In the handling of this apparatus. With the control knob in the charge and operate position full voltage of the bridge (500 volts) Is applied to the positive and low terminals and through the test leads to the electrodes. Do not attempt to handle the electrodes of the test leads unless the oontrol knob is in the "CHECK" position. Possible penalty for failure to observe this precaution -- Painful Shock. 5...METHOD NO. 10,126 "CORROSION AND CHEMICAL STABILITY." a. Apparatus: G.B. Corrosion Apparatus consists of the following: 1) A Corrosion Plask - It Is a 300-ml. Pyrex flask 50 TOWOLDMONOQ23037 with a ground glass 24/40 Joint equipped with a 12-inch straight tube as an air cooled con denser. The air-condenser is painted on the outside with aluminum. 2) The CorroBlon Apparatus: A transite box 32" long x B" wide J 5` deep. The top of the box represents a split transite board with 5 holes cut to fit the flasks. The box is heated by two 500-watt, 15 volt Q.E. Strip heaters with off-set terminals at one end (23.5" overall length). The heating length of the heating element is covered by a copper strip 19-1/2" long x 4" wide x 1/4" thick. The temperature is controlled by an automatic thermostat with temperature setting indicator. h. Procedure: 1) Roll a rectangular (2" x 4") piece of aluminum foil so that it will pass through a ground glass 24/40 Joint of the corrosion test flask. CAUTION: Be careful that after rolling the specimen does not touch Itself at any point. 2) Wash the aluminum foil (Step 1) scrupulously with acetone, distilled water, acetone, benzene, and chloride-free ether. 3) Then place the foil on a clean watch-glass and dry in an oven at 110C. for 30 min. After cleaning handle the specimen with tongs or forceps only. 4) Weigh accurately on an analytical balance the specimen (Step 3) at room temperature. 5) Drop the weighed aluminum foil into the chloridefree corrosion flask of the "G.E. CorroBlon Appa ratus." Rinse out flask with sample and rinse end of condenser with sample. 51 TOWOLDMONOQ23038 6) Add 200 ml. of the product under test to the aluminum foil (Step 4 and 5). 7) Set the corrosion flask In the corrosion test appa ratus . 8) Attach a 12-lnch straight-tube air-cooled condenser, the outside of which Is painted with aluminum. 9) Cover the exposed part of the flask with aluminum foil. IQ) Heat the flask for 6 (+ O.l) hours at 210 5) C. The temperature of the liquid in the test flask Is mea sured Indirectly using a thermometer Inserted through a cork stopper and Into similar liquid contained In an Iden tical flask seated adjacent to the test flask on the heating chamber. 11) At the end of the heating period, detach condenser from the flask before removing It from the hot plate. 12) Remove the flask from the hot plate and cover all of the flask with aluminum foil (when the flask is not on the hot plate.) 13) Without removing the aluminum foil covering of the flask, analyze the product (Step 6) remaining In the corrosion apparatus for: a) Appearance, Color, and Condition. b) Inorganic (Free) Chlorldes--Apply Method No. 10,118 c) Acidity (Acid Number) - Follow Method No. 10,087 14) With a pair of clean, straight nlchrome tongs, remove the aluminum foil specimen (Step 5) wash thoroughly, dry and weight accurately on an analytical balance In the same manner as before (Steps 2, 3 and 4). Report the corrosion as loss or gain In weight to the nearest 0.0001 g. and the Chemical Stability, as Indicated by the ana lysis of the products "After Corrosion Test", In the same way as reported for the original (as received) material. 51 A 01*4318 TOWOLDMONOQ23039 6. METHOD NO. 10,118, "INORGANIC CHLORIDES." a. Preparation of Standards: 1) Make a primary standard of 100.0 ppm by weighing 0.1648 g. C.P. NaCl Into a chloride-free 1 liter volumetric flask. Dilute to the mark and mix thoroughly. Make a 10.0 ppm standard by diluting 100 ml. of the primary standard to 1 liter, and mixing well. For every 0.1 ppm standard, dilute to 10 ml. of the 10 ppm standard to one liter and mix well. A 0.1 ppm beam is considered the very faintest beam perceptible to the eye between 15-45 seconds after adding the AgNO, solution. If the beam intensity is not vlslble^at all, or if easily visible (too strong), discard the solutions and make new standards. 2) Weigh 20.0 g, C.P. AgNC>3 into a chloride free dark bottle. Add 20 ml. C.P. HNO- (chloride-free). Dilute to 200 ml. with water. 3) All solutions should be freshly prepared every two weeks and stored In glass-stoppered Pyrex bottles. b. Light Source: Employ the 2 battery Penllte flashlight, having a 3-4 mm. light aperture. New batteries must be used fre quently in order to perceive beams properly. c. Procedure: 1) Thoroughly rinse two separatory funnels with chloride-free water three or four times. Then take an aliquot from each funnel in a test tube which has been rinsed with chloride-free water. Test these aliquots for Tyndall beams by adding 3-5 drops of AgNOo and allowing 45 sec. for full beam to evolve. Absolutely no dust or chloride beam should be present. (Tf beam is present, rinse all equipment with 1:1 HNO3 and repeat Step 1). 2) When funnels are beam-free, drain out all the water except 50 ml. in one and 25 ml. in the other. Heat the water in both funnels to boiling. (Hold stopper while heating as steam may cause stopper to fail.) 52 TOWOLDMONOQ23040 3) Transfer 50 ml. of the sample from the sample bottle at a temperature of 95-100C. Into the separatory funnel containing the 50 ml. of boiling water. (As a precautionary measure, pour some of the sample from the sample bottle Into a waste beaker before adding the 50 ml. to the funnel.) 4) Stopper the funnel and shake vigorously for at least 1 minute, venting frequently through the stopcock. (Care must be exercised at all times to touch neither 'the lower part of the funnel stem not the ground part of the stopcock.) 5) Allow the layers to separate and drain off the sample Into the second funnel containing the 25 ml. of boiling water. (As before, drain off a few ml. of the sample Into a waste beaker before draining the sample Into the second separatory funnel.; It may be necessary to heat the sample when transferring the sample to the second funnel; e.g., Aroclor 1260. 6) Repeat step 4 and allow the layers to separate. Then drain off the sample Into a waste beaker. 7) Combine both water extracts In one funnel and shake thoroughly. 8) Take approximately a 10 ml. aliquot of the water extract out through the bottom of the funnel Into a 3/4" x 6" test tube. Again, first allow a few ml. to drain out before taking the aliquot. (The test tube used should be rinsed with chloride-free water several times before using.) 9) Add approximately an equal portion of chloridefree ether. (The ether Is tested by shaking a portion of it with chloride-free water and testing for Tyndall beam at the end of 45 sec. If beam is present, wash ether several times with chloridefree water until washings show no beam after adding 3-5 drops AgNOg). 10) Shake the ether-water mixture until the emulsion In the sample disappears and the water layer is completely beam free before adding AgNOg. If emulsion is difficult to break, add sample dropwise through the ether and then shake. 53 01**320 TOWOLDMONOQ23041 11) Add 3-5 drops of 10# AgNO? solution and test for ohlorlde beam for 45 sec. exactly. If no beam Is present at the end of 45 seconds, report as ^0.1 ppm. The very faintest of beams Is considered 0.1 ppm. If beam Is stronger It will be necessary to compare with standards of 0.15, 0.20 up to 1.0 ppm, adding the 3-5 drops of AgNOo and comparing at the end of 45 sec. The method Is precise to the nearest 0.1 ppm. Report results to the nearest 0.1 ppm. 7. METHOD NO. 10,087, "ACID NUMBER." a. Reagents: 1) Nitration grade benzol. 2) Anhydrous methanol. 3) A saturated solution of phenol red (phenol sulfonphthalein) In methanol (approx. 0.1#). 4) A 0.01 N solution of KOH In methanol. b. Procedure: 1) Place 100 ml. of benzol, 100 ml. of methanol and 0.5 ml. (pipette) of phenol red Indicator Into one of two clean dry 500 ml. Erlenmeyer flasks. 2) Neutralize carefully with the 0.01 N KOH (to be first definite pink color.) 3) Pour the mixture back and forth between the two flasks several times. If the solution is still neutral, divide It equally between the two flasks. If not, repeat steps 2 and 3 4) Weigh ( 0.05 g.) Into one of the flasks a 75.0 T 5.0 g. sample and titrate with the 0.01 N, KOH until the sample matones the blank. o.. Calculations: Acid No. (mg. KOH/gram sample) . ml. 0.01 N KOH x '0.56 Sample Weight' 54 01*4321 TOWOLDMONOQ23042 Report the results to the nearest 0.001 If they are below 0.1, otherwise to the nearest 0.01. The method is precise to + 0.002 for acid numbers below 0.01 and to + 0.01 In the range of 0.1 to 0.01. NOTE 1: To convert mg. KOH/gram to mg. NaOH/gram, multiply by 0.715. 8. METHOD (MODIFIED NO. 10,620, "MOISTURE (WATER)". a.Introductory Comment: The Karl Fischer Reagent titration method used in the analytical laboratory involves use of an analytical ba lance to weigh accurately about one drop of water used in preparing the standard. Since an analytical balance may not be available, the method has been modified and sues a purchased standard water solution as described below. Also, in the laboratory a "Dead Stop" potentiometric method for determining the end point is often used. However, as this equipment may not be available, the procedure described below uses the visual indicator change for determining the end point. b.Apparatus and Reagents: 1) Karl Fischer Burett, Automatic Pyrex No. 5750, 25 ml. capacity. Ace Glass Company, Vineland, New Jersey. 2) Water Standard in Methanol. No. SO-W-2 (l ml. 1 mg. H_0) Fisher Scientific Company, 2800 Jeffer son Avef, St. Louis, Missouri. 3) Karl Fischer Reagent Solution No. SO-K-2, Fisher Scientific Company. c.Standardization of Karl Fischer Reagent Into a 500 ml. clean, dry Erlenmeyer flask, place about 100 ml. "Anhydrous" methoanol (commerically available, 99-95?^). Add Karl Fischer reagent to this blank until the first color change from lemon yellow. It Is not necessary to read the burette at this point. Carefully pipette 50 ml. of standard watersolutlon into the blanked methanol. Refill the Karl Fischer burette.Titrate the solution with gentle swirling to mix, until the same color is obtained as was obtained for the blank. Now read the burette. . 55 TOWOLDMONOQ23043 Moisture value of K.F. reagent In terms of grams H20 per ml. (Moisture value of stand(Ml. Standard H20 solution) ,ard water solution In gm. per ml. stated on label.) ml. Karl Fischer Reagent Solvent Mixture: Since the solubility of the different askarels varies, the following solvent mixtures are suggested: Material Anhydrous Benzene Anhydrous Methanol Pyranol 1478 Pyranol 1488 1467 Pyranol 1481 Pyranol 1495 All Aroclors 0 ml. 100 ml. 100 ml. 100 ml. 110 ml. 300 ml. 200 ml. 200 ml. 200 ml. 190 ml. Procedure, "Visual End Point." 1) Place 100-300 ml. of dry solvent mixture (c) in a dry 500 ml. ground glass stoppered Erlenmeyer flask. 2) Titrate the solvent with K.F. reagent to the vis ual endpoint, i.e., the first change from the yellow to reddish orange that persists for 30 seconds. Refill the burette. 3) Using a beam balance, weigh to the nearest 0.1 gram by difference, a sample containing 0.03 to 0.06 grams H20 Into the flask. 4) Stopper and shake until the sample Is in solution. 5) Titrate the solution with K.F. reagent to the endpoint described in Step 2. Record the volume of K.F. reagent used. Calculation: HoO ml. of K.F. reagent x HoO factor x 100 ' Sample Weight References: Mitchell, J. and Smith, D.M., Chemical Analysis, Vol Aquametry, Interscience Publishers, Inc., New York, (1948) 56 01**323 TOWOLDMONOQ23044 CHAPTER 7 TYPICAL PROPERTIES The 1200 series members of the Aroolor family are chlor inated biphenyls, and are made by chlorinating biphenyl to approximately the peroehtage of chlorine, by weight. In dicated by the last two digits of the serial number. For example, Aroolor 1254 Is approximately 5458 chlorine on a weight basis. Accordingly, these Aroclors are not single or simple compounds. They are a mixture of Isomeric com pounds oomposed predominately of the chemical compound In dicated below as being their approximate equivalent: Aroolor 1242 Aroclor 1248 Aroolor 1254 Aroclor 1260 Trlohloroblphenyl Tetraohloroblphenyl Pentaehloroblphenyl Hexachloroblphenyl For transformer use and some capacitor use where lower viscosity Is required for better low temperature operation than offered by the above Aroclors, these products are mixed with pour point depressants, particularly triohlorobenzene resulting in various General Electric Company Pyranols described briefly as follows: Transformer Pyranol 1467* 6056 of Aroolor 1260 4oj6 of Elec. Grade Triohlorobenzene 0.125SK of Tin Tetraphenyl Transformer Pyranol 1470* 45# of Aroclor 1260 55j8 of Elec. Grade TrlohloroTetrachlorobenzene Mix ture 0.12558 of Tin Tetraphenyl *0se of tri-tetraohlorobenzene and tin-tetraphenyl scavenger is subject tb G.E. patents and license: Royalty arrangements should be checked before using. Questions about license concerning the use of anthraquinone stabilizer for DC capacitors should be referred to Western Electric, 195 Broadway, N.Y.C. 57 01443^4 TOWOLDMONOQ23045 Capacitor Pyranol l48l 75# of Aroelor 1254 25# of Elec. Grade Tri chlorobenzene Detailed properties of all of these produots are given as follows: AROCLOR 1242 PROPERTY TYPICAL Viso. 9 37.8C. (ASTM d88) Specifio Gravity @ 25/15.5C. (ASTM D287) Color, APHA Condition Acidity, mg. KOH/g. Pour Pt., C. (ASTM D97) Inorganic Chlorides, ppm. Refractive Index @ 25 C. Distillation Range (ASTM D20) Corrected for stem and barometric pressure Corrosion 82 - 92 seoonds Saybolt Dniver. 1.381 - 1.392 100 max. Clear 0.01 max. -14 or lower 0.10 max. 1.6245 - 1.6265 lOje 325C. min. 90# 36oC. max. After heating with aluminum for six hours at 210C i 10oc, the aluminum must not be cor roded either on visual or weight inspection and the Aroelor 1242 should meet the following specs: Color, APHA 150 max. Acidity,mg.KOH/g. 0.01 max. Inorg.Chlorides,ppm 0.10 max. Condition Clear Water Content, ppm 35 max. Resistivity 1000c. 500 volts DC @ 0.1" gap 500 x 10^ ohm-om., min, Dieleotric Constant 100C. @ 1000 cycles (ASTM D924) 4.7 - 4.9 Flash Point Cleve. Open Cup* 160C,, min. Fire Point C.* None to boiling point Sulfates (ASTM-D117-31)* None Fixed chlorine content (Carius)* 41.5 42.5# Specific Heat 9 2C.* 0.29 Evaporation @ 100C for 6 hrs.* 0.4# max. Dieleotric Strength (KV) 35 Min. (ASTM D877)* *Not determined unless by special request. 58 01*4325 TOWOLDMONOQ23046 AROCLOR 1248 PROPERTY Vise. @ 54.4C. (ASTM D-88) Spec. Orav. <8 65/'15.5C. (ASTM D-287) Color, APHA Condition Acidity, mg. KOH/g. Pour Point C. (ASTM D-97) Refrao, Index @ 20C. Diet. Range (ASTM D-20) Water Content, ppm. Reals. 100C. 500 v D.C. @ 0.1" gap Dielectric Constant,100C. 1000 cycle Dlelectrlo Strength 25C.* Plash Point, (C.O.C.)* Fixed Chlorine (Carius)* Specific Heat @ 25C.* TYPICAL 73-80, sec.Saybolt Unlver. 1.404-1.414 100 max. Clear 0.01 max. -7 1.630-1.6R1 343 - 373C. 35 500 x 10^ ohm-cini min. 4.6 35 KV min. 193C. 47.5 - 48.5# 0.27 Not determined unless by special request. 59 TOWOLDMONOQ23047 AROCLOR 1254 PROPERTY TYPICAL Vise. @ 98.9C.(ASTM D88) Specific Gravity @ 65/15.5C. (ASTM D287) Color, APHA Condition Acidity, mg.KOH/g. Pour Pt. C.(ASTM D97) Inorganic Chlorides, ppm. Refraotlve Index @ 25C. Distillation Range (ASTM D20) Corrected for stem and Barometric Pressure Corrosion 44-48 sec. Saybolt Onlver. 1.495 - 1.505 100 max. Clear 0.01 max. 7-12 0.10 max. 1.6370 - 1.6390 10* 366-- 378C. 5056 372 - 3830c. 90* 383 - 396C. After heating with aluminum for 6 hours @ 210C. plus or minus 10C, the aluminum must be cor roded either on visual or weight Inspection and the Aroolor 1254 should meet the following specs: Color, APHA 150 max. Acidity,mg.KOH/g. 0.01 max. Free Chlorides,ppm.0.10 max. Condition Clear Water Content, ppm. 35 max, Resistivity 100C.,500 v D.C. @ 0.1" gap 500 x 10* ohm-em., min. Dielectric Constant, 100C 4.15 - 4.35 1000 cycles Dleleotrlo Strength 25C* 35 KV., min. Burn Point (ASTM D92)* Higher than 350C. Sulfates (ASTM D-117-31)* None Fixed Chlorine Content (Carlus)* 55 t 0.5* Evaporation @ 100C. for 6 hrs<$ 0.4* max. Stability* There shall be no liberation of chlorine or chlorides when the material Is heated @ 100C In glass vessels In contact with air for periods of at least one month. Ageing Characteristics* No loss In resistivity over original value on heating In air for 96 hrs. at 100C. Specific Heat @ 25C.* 0.26 Not determined unless by special request. 60 0l4*3<f7 TOWOLDMONOQ23048 AROCLOR 1260 PROPERTY TYPICAL Vlso. @ 98.9C.(ASTM D88) 72 - 78 Seo. Saybolt Onlv. Specific Gravity @ 90C./15.5C 1.555 - 1.566 (ASTM D287) Color, APHA 150 max. Condition Clear Acidity, mg.KOH/g. 0,01 max. Pour Pt.,C.(ASTM D97) 25 - 3^ Inorganic chlorides, ppm. 0.10 max. Refractive Index, 25C. 1.6455 - 1.6470 Distillation Range (ASTM D20) 1056 385 - 398C Corrected for stem and 50* 390 - 404C. barometric pressure. 9056 400 - 420C. Corrosion After heating with aluminum for 6 hrs. @ 210C. + 10C. the aluminum muBt no be cor roded either on visual or weight inspection and the Aroclor 1260 should meet the following specs: Color, APHA 150 max. Free Chlorides,ppm. 0.10 max. Acidity,mg.KOH/g. 0.01 max. Condition Clear Water content, ppm. 35 max. Resistivity,100C. 500 volts @ p.l" gap _ 500 x 109 ohm-cm., min. Dielectric Strength 50C.* 30 KV., min. Dielectric Strength 100C.* 30 KV., min. Dielectric Constant 100C. 3.6 - 3.8 @ 1000 cycles* Burn Pt. (ASTM D92)* Higher than 350C. Sulfates (ASTM D117-31)* None Fixed chlorine content (Carius)* 60 + 0.5* Evaporation @ 100C. for 6 hrs.* 0.2* max. Stability* There Bhall be no liberation of chlorine or chlorides when . the material is heated @ 100C. in a glass vessel in contact with air for periods of at least one month. Specific Heat @ 25C.* 0.23 *Not determined unless by special request. 61 014*328 TOWOLDMONOQ23049 PYRANOL 1481 PROPERTIES TYPICAL Viscosity 37.8C. 70 - 82 sec. Saybolt Unlv. Spec. Gravity @ 15.5/15.5C 1.525 - 1.535 Color, APHA 150 max. Condition Clear Acidity, mg. KOH/g. 0.01 max. Pour Pt., C. -15 or lower Inorganic Chlorides, ppm. 0.10 max. Refractive Index 25C. 1.6205 - 1.6215 Distillation Range Corrected for stem and barometrio pressure. First drop 205C. min. 25# max. Below 270C. 90# 380 - 395C. Corrosion Test Change in Weight 0.0# Color, APHA 200 max. Acidity, after test,mg.KOH/g 0.01 max. Free Chlorides,ppm. 0.10 max. Condition after test Clear Water Content, ppm. 35 max. Resistivity 100C 500 volts, DC, 0.1"gap 100 x 109 ohm-om.,min. Dielectric Constant (100C., 1000 cycles) 4.1 - 4.6 62 01**329 TOWOLDMONOQ23050 PYRANOL 1467 PROPERTIES TYPICAL Viso. @ 37.8C.,(ASTM D88) 54+2 sec. Saybolt Univ. Speoiflc Gravity @ 15.5/15.5C (ASTM D-287) 1.560 - 1.568 Color, APHA 150 max. Condition Clear Acidity, mg, KOH/g. 0.01 max. Pour Point, C. (ASTM D-97) -32C. or lower Inorganic Chlorides, ppm. 0.10 max. Refractive Index @ 25C. 1.6137 - 1.6147 Distillation Range (ASTM D20) 1st drop - 200C. min. Corrected for stem and Below 270C. - 40 max. barometric pressure 90# - 395 - 4l5C Corrosion After heating with aluminum for 6 hrs. at 200-220C.,the aluminum must not be corroded either on visual or weight in spection and the Pyranol should meet the following specs: Color, APHA 200 max. Acidity,mg.KOH/g. 0.01 max. Inorganio Chlorides 5 max. ppm. Condition Clear Water Content, ppm. 30 max. Resistivity, 100C. 500 volts, 0.1" gap 100 x 10^ ohm-em.,min. Dielectrio Strength, 25C. 35 KV., min. Dielectric Constant, 100C. 1000 cycles* 3.7 - 4.0 Tin Tetraphenyl* Q.125# 4 O.'OljC by weight Burn Point, (ASTM D92)* None up"to Boiling Point Fixed Chlorine* 59.1# min. Arc Formed Oases* Less than I.O56 (Oxygen Free Liquid @ 25C.) Total combustible gases including carbon monoxide, hydrogen and volatile hydro carbons . Not determined unless by special request. 63 01M33O TOWOLDMONOQ23051 PYRANOL 1470 PROPERTIES TYPICAL Vise. 9 37.8C. (ASTM D88) Spec. Gravity @ 15.5/15.5C., (ASTM D287) Color, APHA Condition Acidity, rag. KOH/g. Pour Pt.,C., (ASTM D97) Inorganic Chlorides, ppm. Refraotive Index @ 25C. Distillation Range (ASTM D20) Distillation Range (ASTM D20) Corrected for stem and barometric pressure First drop 3556 55* 65* 95* Corrosion 41-45 Sec. Saybolt Univ. 1.563 - 1.571 150 max. Clear 0.01 max. -44C., or lower 0,10 max. 1.6075 - 1.6085 210OC., min. 238 - 256C. 275 - 345C. 380 - 4ooc. 390 - 4l5c. After heating with aluminum for 6 hrs. @ 200-220C., the aluminum must not be corroded either on visual or weight inspection and the Pyranol should meet the following specs: Color, APHA 200 max. Acidity,mg.KOH/g. 0.01 max. Inorg. Chlorides,ppm 5 max. Condition Clear Water Content, ppm. 30 max. Resistivity, 100C., 500 v., 0.1" gap ,, 100 x 10^ ohm-cm., min. Dielectric Strength, 25C. 35 KV., min. Dieleotric Constant, 100C., 1000 cycles* 3.8 - 4.3 Tin Tetraphenyl* 0.125* + 0.01* by weight Burn Point, (ASTM D92)* None up~to Boiling Point Fixed Chlorine* 60.5 i 0.5 Arc Formed Gases* Total"combustible gases in (Oxygen Free Liquid 9 25C. cluding carbon monoxide, hydro gen and volatile hydrocarbons. Electrical Stability* After heating for 96 hrs. @ 100C in a closed container, the resistivity should not decrease more than 10* Not determined unless by special request. 64 014*331 TOWOLDMONOQ23052 PYRANOL 1488 Vise. @ 37.8C. ,, Speo. Orav. @ 15.5/15.5C. Color, APHA Aoldlty (Mg KOH/g) Water, ppm. Condition Refrac. Index @ 25C. Free Chloride, ppm. Pour Point, C, Reels. @ 100C., 500 v D.C. 1" gap Dlelectrlo Strength (25C.) Corrosion: Loss of Aluminum Dielectric Constant @ 1000 cycles @ 100C.* Distilling Range (corrected)* 1st drop Below 270C. 90# point Burn Point (ASTM D-92)* Fixed Chlorines* Arc Formed Oases* (Oxygen-free liquid @ 25C.) Not determined unless by 54-- 2 Sec. Saybolt Unlv. 1.560 - 1.568 150 max. .014 max. 35 max. Clear 1.6137 - 1.6147 0.10 max. Lower than -32C. 100 x 10^ ohm-cm min. Over 35 KV None Heating with aluminum for 6 hrs. at 200-220C. The Pyranol after heating Bhould meet the following specB: Color, APHA 200 max. Acidity(MgKOH/g) .014 max. Free Chlorides ppm .10 max. Condition Clear 3.7 - 4.0 200C. min. 40# max. 295 - 4l5C. None up to boiling point 59.1# min. Less than 1.0$ total com bustible gases Including carbon monoxide, hydrogen, and volatile hydrocarbons, il request. 65 01*4 332 TOWOLDMONOQ23053 CHAPTER 8 EARTH TREATMENT OP AROCLOR IN THE ELECTRICAL INDUSTRY PRIOR TO USE. Aroclors and their mixtures supplied to the electrical Industry must conform with most strlot requirements sepoifled by the industry as shown in Chapter 7. Since these products are sensitive to contamination from traces of impurities, they require careful handling in the Industry when sampling or storing or using the materials to Impregnate capacitors or fill transformers. Common contaminants to be avoided Include moisture, ionizable impurities, metallic impurities, such as rust or corrosion products from storage and handling equipment, and contaminants such as oils (mineral oils), lubricating oils or greases common ly used in equipment or other processes in the electrical industry. Care must be taken to avoid contamination from contact with Improper gaskets or packing materials, including natural and synthetic rubber and moBt plastic exclusive of certain Silicones and Teflon. Rosin solder fluxes, etc. may also introduce traces of deleterious impurities. The dielectrics are also susceptible to the harmful action of ultra-violet light and, therefore, exposure to direct sunlight should be avoided. The adverse effect of lonlzable impurities is especially pronounced in the low visoosity Aroolors such as Aroclor 1242 66 0144(333 TOWOLDMONOQ23054 or Aroclor mixtures such as Pyranol l48l. In the case of more viscous fluids, such as Aroclor 1254, the lonizable Im purities are not so free to move about In the fluid and, con sequently, the more viscous fluids can be handled with less care than required for the thinner fluldB. This Is especially pertinent In capacitor manufacturing. When using the thinner type Aroclors to make capaoltors that offer superior low temperature operation, the following typeB of traoe contamination affecting the electrloal properties of the dielectric have been experienced. Occasional droplets of perspiration from operators, when winding the capacitor cores, have fallen onto the paper causing contamination In the finished unltB. Small amounts of Glyptal resin and simi lar sealing compounds used to seal tiny leaks In the vacuum Impregnating equipment or storage tanks have caused contamina tion. Also, small amounts of mineral oil entering the system have caused similar trouble. A small droplet of any of these materials In one or several liters of the thinner type fluids results in noticeable contamination, whereas it may not have as much adverse effect on the more vIscoub dielectrlos. To be certain that the fluids are free from traoes of contamination, it Is standard practice to treat them with con ditioned dlatomaceous earth and then to filter immediately be fore use. Treatment with this earth by removing trace contam inants results in "up-grading" the electrical values, e.g., 67 01^^33*1 TOWOLDMONOQ23055 the volume-resistivity may be brought up considerably beyond the specification minimum or the normal values of the dielectric as received. Likewise, Improvement in power factor may be ao compllshed. The earth treatment recommended for use by the electrical manufacturers is qualitatively the same as used in the produc tion of the Aroclors and their preparation for shipment to the electrical industry. Treatment of the Aroolors with earth by the electrical manufacturers is a step required to assure that traces of impurity or contamination that may have been introduced during storage or handling In the electrical indus try have been removed and that maximum electrical values have been attained immediately before the dielectric is introduced into capacitors or transformers. It is impractical for the manufacturer to furnish these dielectrics to the customer at the maximum attainable electrloal qualities because even with careful packaging, shipping, sampling and handling in the electrical Industry, these fluids may easily pick up traces of contaminants from opened tankcars, drums, pipe line, pumps, etc. However, as supplied according to the specifications, the fluids are readily "up-graded" by the earth treatment. The type of diatomaeeous earth used is known as Puller's Earth, supplied by the Ploridin Earth Company, Warren, Pennsyl vania, or the Attapulgus Division, Mineral & Chemicals Corp. of Amerloa, 210 West Washington Square, Philadelphia 55, Pa., 68 01**335 TOWOLDMONOQ23056 or their equivalent. Usually a minus 200 mesh size, regular volatile, 1b used and the quality should be specified as for use by the electrical Industry. (Code 73122) The earth as received needs to be conditioned and acti vated, after which It should be stored only a minimum length of time (about a day at the most) and In hermetically sealed containers, prior to use. It Is desirable that the earth be UBed Immediately after It has been activated. \ Activation should be done by heating the earth contained'. In stainless steel shallow trays for four hours (^t^400C^) In \ a muffle furnace. If a muffle furnace Is not available or the oapaclty by this method may not be great enough, the earth can be activated by heating at least twelve hours In an elec- i trlcally heated oveni<(a^tt^j225S0O^C^,,)>..Another method used Is to pan / jdry and activate by heating ^J.00C^)and using a strong vacuum, about 6 mm. of mercury. This latter method Is used In connection with transformer work and the former methods arp usually used for capacitor work, --------- -In-theTSlfice of pan drying* rotary driers may be used but their aotlon should n6t be so severe as to break the earth par ticles to the extent of producing powder which Is difficult to handle In the subsequent filtering operations. It Is the consensus that the earth should not be heated above 400c. as this may cause collapse of the particles. 69 0144336 TOWOLDMONOQ23057 The amount of earth used is usually 0.1$ to 0.356 based on the weight of the fluid. Larger amounts of earth can be used If the fluid Is composed of only Aroclor or a mixture of Aroolor and ohlorinated benzene or other pour point depressants. However, larger amounts of highly active earth. In the range of 2% or 3$, would be expected to selectively adsorb scavengers or stabilizers from the fluids containing these additives. This Is especially of oonoern In handling the transformer fluids whloh usually contain scavengers such as tin tetraphenyl. For transformer work It Is suggested that the earth be condi tioned and mildly activated by heating It at 100C. under va cuum, about 6 mm. of mercury. Not more than about 0.1$ of earth based on the total weight of the transformer fluid should be used. For treatment with earth, the fluid Is put Into a suitable tank fitted with an agitator, heating coll, and a cover. The proper amount of freshly conditioned earth Is added and the mixture Is agitated thoroughly and heated for about four hours. The more viscous dielectrics such as Aroclors 1248 and 1254 Are heated at about 70 to 80 C. (158 to 176F.) and the less vlsoous materials such as Aroclor 1242 and Pyranols 1481, 1467, and 1470 are heated at about 50 to 60 C. (122 to l40F.) After about four hours contact the material Is filtered through a Sparkler or Sweetland or a comparable filter press previously fitted with filter paper liners such as supplied by 70 01*4337 TOWOLDMONOQ23058 Carl Schleicher and Schuel Co,, Inc,, Keene, N.H. The paper Is usually 25 milB thick and must be dried at 100C. to remove moisture, prior to uae In the filter press. The filtered dleleotrlo material Is then ready for Impregnating capacitors or filling transformers. In some cases, especially for AC capacitor work where the dielectric does not require addition of stabilizers and accordingly there Is no danger of removing such additives by repeated earth treatment, good practice Is to use continuous earth treating, circulation and filtration with constant read ing of the resistivity of the filtered dielectric. In Chapters 1 and 2 selection of proper materials of construction for the tankcars and storage tanks was discussed. It Is equally Important to select proper materials of con struction for the processing tanks used In the oapacitor and transformer Industries and also for the lmprgnating chambers used In making oapacltors. It is preferable that this equipment be made of stain less steel or aluminum, or , If It Is of steel construction, the Interior should be either zlno-tln metallized or aluminum lined. While Iron or steel equipment Is not regarded as de sirable for handling the fluids, this type of construction is used in some of the plants. Here the possibilities of rust ing or corrosion cannot be overlooked. If the equipment Is kept free from water and if a film of clean dleleotrlo adheres 71 01*4338 TOWOLDMONOQ23059 to the surface of the metal* e.g. when the tanks are empty, then satisfactory operation oan be experienced. However, a number of factors must be kept In mind and to cite an example, reference Is made to the Impregnation of capacltors by the chamber method. The moisture content of the paper used In the capacitor cores may easily Introduce several gallons of water Into the average Impregnating ohamber. This water 1b removed from the oapaoltors prior to Impregnation -- usually by heating the chamber to about 130C. under efficient vacuum, 100 microns or less. If the ohamber Is not made of the preferred materials of construction, slight corrosion may occur and the film of fluid on the Interior surfaoe of the tank may be contaminated and In turn Introduce traces of impurities Into the treated and clean dielectric subsequently Introduced Into the chamber for Impregnating the capacitors. In fact, because of thlB possibility of contamination. In some operations the capacitors are conditioned and dried preparatory to Impreg nation In a separate oven or chamber and when thoroughly dried they are then transferred Into a second chamber used for Impreg nation. In the case of relatively large size capacitors, such as power factor correction units, a manifold pipe system may be used to handle each unit Individually rather than by the batohchamber method. The unimpregnated capacitors are placed Into an oven and vacuum Is applied to the Individual units attached to the manifold. 72 0144339 TOWOLDMON0023060 When conditioned and dry, the dielectric is introduced into the unit through the manifold. Care must be taken that moist air or contaminants do not collect in the branch through which the dielectric is introduced. In addition to removing moisture, another purpose of the heat and vacuum conditioning treatment given the capacitor units prior to Impregnation is to remove traces of impurities such as residual solvent from the metal cleaning operations and from solder flux, etc. The fluid is introduced hot into the evacuated capacitor units. The more viscous Aroolors, such as 1248 and 1254, are usually Impregnated at 85 to 130C. The less viscous and more volatile dielectrics such as Aroclor 1242 and mix tures of Aroclor with chlorinated benzene may be introduced best at lower temperatures -- about 50C. optimum, 80<t. max. Table IV indicates desirable minimum resistivity values of the dieleotrio materials when earth treated and ready for oapacltor impregnation and similar values of the material following the process. TABLE IV Dielectric Volume Resistivity Ohm-om at 100C, and 500 volts DC. Prior Stoo After Impregnation Impregnation Aroolor 1254 2.500 x 109 800 x 109 Aroclor 1242 1.500 x 109 600 x 109 Pyranol l48l 600 x 109 400 x 109 73 Ol't'tS'lO TOWOLDMONOQ23061 In the case of new and freshly filled transformers using Aroclor dielectric mixtures. It seems reasonable that the power factor of a sample of the fluid drawn from the trans former should be In the range of about 5 to 12 per cent, measured at 60 cycles and 100C. With field service of the transformer the power factor value Is expeoted to Increase somewhat. However, such a power factor lnorease alone does not seem to have harmful effeot on the operation of the transformer. A more usual measurement used for transformer fluid Is volume-resistivity. This value of the new dielectric prior to filling the transformer should be about 500 x 109 ohm-cm. at 1,000 oyoles and 100C. The similar value of the fluid taken from a new transformer should be atleast, about, 50 x 109 ohm-cm and no lower than 25 x 109 ohm cm. With long field service volume-resistivity values de crease somewhat but seem to level off around 10 x 109 ohm-cm, with satisfactory transformer qperatlon. However, If the volume-resistivity of the fluid falls below 10 x 109 ohm-cm, the matter should be looked into. 74 TOWOLDMONOQ23062 CHAPTER 9 DERMATOLOGY AND TOXICOLOGY Skin patoh tests using Aroolor 1254 (biphenyl Chlorinated to the extent of 54$ by weight) applied to gauze and placed in oontact with the skin showed no primary irritancy or sen sitization. The tests were conducted under competent medical supervision and the standard procedure reoommended by Drs. Louis Schwartz and Samuel M. Peek, Reprint No. 2552, Public Health Reports, Vol. 59, No. 19 (April 28, 1944) was used. If Aroolors are spilled on the skin, the skin should be washed in the usual manner with soap BolutionB. If accidental burns occur from contact with hot Aroolors, the burn should be treated the Bame as any ordinary burn. Aroclor adhering to the burned area need not be removed immediately unless treatment of the burn demands it, in which case use soap and water or repeated washings with a vegetable oil. At ordinary temperatures Aroolors have not presented industrial toxicological problems. If Aroolors are used at elevated temperatures in open systems, methods must be designed to exhaust any vapors arising. Experimental work on animals indicates that the maximum safe concentrations of vapors in workrooms is in the range of 1.0 to 2.0 milligram per cubic meter of air. This applies to all of the liquid Aroolors. 75 01 44342 TOWOLDMONOQ23063 Laboratory technique merely requires keeping the hands free of the liquid and handling It under a well ventilated hood. Localized or spot ventilation together with general work room exhaust Is recommended for plant operations. When sampling tankcars, canvas gloves and safety glasses or goggles should be worn. No speolal clothing Is required but the worker's garments should be laundered at least weekly and changed In case Aroclor or Aroclor mixture Is spilled on the clothes accidentally. If workmen are exposed to Aroclor vapors at relatively high levels, as may be the case when opening a heated capacitor impregnating chamber, a respirator should be worn during these short intervals. The many years of satisfactory and safe use of Aroclors and their mixtures with ohlorinated benzenes in the electrical Industry for Impregnating capacitors and filling transformers has demonstrated the Industry's ability to handle these fluids without hazard to the workmen. It is a simple matter and in line with good "housekeeping" and personal cleanliness to exercize the suggested and required precautions In all cases. 76 01*4343 TOWOLDMONOQ23064 TOWOLDMONOQ23065 0144345 TOWOLDMONOQ23066 \ 0144346 TOWOLDMONOQ23067 0144347 1 TOWOLDMON0023068 Vlm Dm*-riACK9148*l itALt- y* l'-o* 0144348 K.rexer*t P***inaa **, t*r*wtSTOMAAntiiiM* * M IMTUW IMJtl Monianta Lhtmieal Lmnpuxy MOAAMATV MVWOH ANNIVTON. ALABAMA me. 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