US2562532A - Storage battery case and composition for molding the same - Google Patents

Storage battery case and composition for molding the same Download PDF

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Publication number
US2562532A
US2562532A US649243A US64924346A US2562532A US 2562532 A US2562532 A US 2562532A US 649243 A US649243 A US 649243A US 64924346 A US64924346 A US 64924346A US 2562532 A US2562532 A US 2562532A
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asbestos
storage battery
composition
molding
around
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US649243A
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Edward R Dillehay
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Richardson Co
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Richardson Co
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10Primary casings, jackets or wrappings of a single cell or a single battery
    • H01M50/116Primary casings, jackets or wrappings of a single cell or a single battery characterised by the material
    • H01M50/121Organic material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10Primary casings, jackets or wrappings of a single cell or a single battery
    • H01M50/116Primary casings, jackets or wrappings of a single cell or a single battery characterised by the material
    • H01M50/117Inorganic material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10Primary casings, jackets or wrappings of a single cell or a single battery
    • H01M50/116Primary casings, jackets or wrappings of a single cell or a single battery characterised by the material
    • H01M50/122Composite material consisting of a mixture of organic and inorganic materials
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10Primary casings, jackets or wrappings of a single cell or a single battery
    • H01M50/131Primary casings, jackets or wrappings of a single cell or a single battery characterised by physical properties, e.g. gas-permeability or size
    • H01M50/134Hardness
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Definitions

  • the ordinary chrysotile asbestos of commerce has a strong fiber but is not acid resistant. Indeed it tends to swell when subject to storage battery electrolyte. There were early trials at making storage battery containers using this asbestos, but they failed, due to acid penetration and swelling arising from the use of this asbestos even though ostensibly protected by the bituminousbinder.
  • Chrysotile asbestos has a fiber which has a surface condition similar to greasiness. Water will not break-it down. Materials do not readily adhere tothe surface nor penetrate the chrysotile fiber, as is the case with organic fiber. Thus the technique of mixing bitumen and chrysotile asbestos into bitumen so as to get the maximum strengthening action of the fiber, is not obvious.
  • the bitumen employed in my novel composition will be of the type used in making composition storage battery containers generally.
  • a blown asphalt blended with gilsonite to have a penetration of 16 (150 F., 5 seconds, grams), and showing a penetration of 11 F., 5 seconds, 50 grams) and 25 (185 F., 5 seconds, 200 grams) may be employed, this blend having a ball and ring melt point of 290 F.
  • I also may employ an asphalt blown oil blend having a ball and ring melt point of 260 F'., and a penetration of only 12 at F., 5 seconds, 100 grams.
  • Other asphalts are usable within the field of hard molding asphalts.
  • the mineral matter aside from the asbestos used in my composition may be an infusorial earth such as celite, or other pulverulent acid resisting mineral matter which need not have any reenforcing effect, the mineral matter being used basically to contribute hardness to the composition.
  • the asbestos used by me will be a good grade Canadian or other chrysotile asbestos such as Grade No. 5K (Canadian classification) of medium fiber length running up to inches in length, and averaging around inches in length. Very long length fiber is not required and simply presents greater mixing problems. A fiber length very much less would result in requiring more asbestos to be used than would be safe to avoid acid deterioration, which among other things, tends to swell the final composition when under acid'conditions.
  • the whole batch may be mixed at one time, or the mineral matter may be mixed with the asphaltic material and the asbestos mixed in subsequently. Or a mineral matter mix andanasbestosmixmaybothbemadeandthe two then mixed together.
  • My preferred practice is to start with the bitumen in fluid condition, 1. e., above its ball and ring melt point, and then add and incorporate the mineral matter which will not be critical as to percentage, but should run to around 38%, since a better molding action is produced if the asphaltic ingredient con-. stitutes around 50% of the entire batch.
  • the asbestos is then wetted with water, or may be added dry to the mixer and water added to the mixer or its equivalent of steam inJected over a period of time.
  • wetting the ashestos I have used with success water in the proportion of 25 pounds to 100 pounds of the asbestos. The lowest permissible moisture would be around by weight and if equal parts asbestos and moisture were used. the proceeding would be unsatisfactory.
  • the amount of asbestos to use will'be not more than around 12 to 13%, and not less than around 7%, otherwise either the box will not stand up if the asbestos is more or will not be stron enough to satisfy requirements, if it" is less.
  • the lower percentage range will require-an asj bestos selected for quite long fiber length.
  • the molding operation is carried outinlthe normal manner for hot molding of storage battery composition containers and the result is to produce a box with a glossy and smooth'exterior which is highly satisfactory as a storage battery container.
  • the individual asbestos fibers will be-separated ln the mixture by films of the asphaltic inaterial, and surprising y. the strength is' fully as a result of the molding operation which requires a long fiow to form the battery partitions.
  • acid proof sprays such as are used in the organic fiber composition cases. e. 8-. acid resistant resins. are more eflective'as a sealer 4 of the surface of the container. a necessity, however, as tests on batteries in ordinary use, have shown no tendency to swell under influence of the electrolyte of the battery.
  • a storage battery container having a monolithic structure formed of hard asphaltic binder, finely divided acid resistant mineral matter, and chrysotile asbestos fiber in an amount of between around 7% to around 13% of the mass, the said finely divided acid resistant mineral matter and the said chrysotile asbestos fiber making up around 50% by weight of the mass.

Description

' July 31, 1951 E. R. DILLEHAY STORAGE BATTERY CASE AND COMPOSITION FOR MOLDING THE SAME Filed Feb. 21, 1946 INVENTOR. EDWAQD .D/L LEN/1K BY ZZZMQ -QZZ ATTOR EYS.
Patented July 31, 1951 STORAGE BATTERY CASE AND COMPOSI- TION FOR MOLDING THE SAME Edward R. Dillehay, Glen Ellyn, 111., assignor to The Richardson Company,- Lockland, Ohio, a corporation of Illinois Application February 21, 1946. Serial No. 649,243
' 6 Claims.. (Cl. 106-202) Lukens, there is described a composition for forming storage battery containers in which organic fiber is employed and distributed in aspecial manner, the top percentage permissible being around to avoid acid penetration of the composition. In addition acid resistant, finely divided, mineral matter is used.
For many years the composition of the Lukens patent has been employed for bituminous composition storage battery containers. In practice from 13 to 15% cotton linters has been the fibrous ingredient. At one time acid resistant asbestos, known as Blue African asbestos, was used as a fibrous ingredient for storage battery containers. This asbestos is not very plentiful and is quite expensive and hence the use of such a fibrous ingredient never attained great popularity. The many types of amphibole asbestos which would apparently be a fibrous ingredient that would withstand the attacks of battery acid, will not serve the purpose, because of lack of fiber strength, as well as relative scarcity.
The ordinary chrysotile asbestos of commerce has a strong fiber but is not acid resistant. Indeed it tends to swell when subject to storage battery electrolyte. There were early trials at making storage battery containers using this asbestos, but they failed, due to acid penetration and swelling arising from the use of this asbestos even though ostensibly protected by the bituminousbinder.
The difliculty with these earlier attempts at .use of chrysotile asbestos arose from the fact that the asbestos was used in too large a quantity, and it was not appreciated that asbestos could be admixed with bitumen in quantities small enough not to be incompletely protected by the bituminous binder, and yet give the required strength for a storage battery container. For example, the 15% limitation given by Lukens in his patent, for the use of acid attackable fiber in a storage battery container, is not a safe criterion for chrysotile asbestos. My investigations have shown that no more than 12% to 13% of chrysotile asbestos may be used.
There is a further complication involved. Chrysotile asbestos has a fiber which has a surface condition similar to greasiness. Water will not break-it down. Materials do not readily adhere tothe surface nor penetrate the chrysotile fiber, as is the case with organic fiber. Thus the technique of mixing bitumen and chrysotile asbestos into bitumen so as to get the maximum strengthening action of the fiber, is not obvious.
The use of water during mixing chrysotile asbestos fiber with bitumen, aids the wetting action of the surface of the fibrous material with the bitumen. However, incidentally, water in too large amounts keeps down the temperature of the bitumen and this makes the bitumen stiff, with the result of breaking up the asbestos fiber into small lengths with the result of cutting down its power of reenforcing and strengthening of the final composition. Thus a technique of mixing which enables the asbestos fibers to be fully coated with the bitumen, and at the same time does not unduly break up the fiber, is quite important, since the possible maximum percentage usable is small.
The bitumen employed in my novel composition will be of the type used in making composition storage battery containers generally. Eor example, a blown asphalt blended with gilsonite to have a penetration of 16 (150 F., 5 seconds, grams), and showing a penetration of 11 F., 5 seconds, 50 grams) and 25 (185 F., 5 seconds, 200 grams) may be employed, this blend having a ball and ring melt point of 290 F. I also may employ an asphalt blown oil blend having a ball and ring melt point of 260 F'., and a penetration of only 12 at F., 5 seconds, 100 grams. Other asphalts are usable within the field of hard molding asphalts.
The mineral matter aside from the asbestos used in my composition may be an infusorial earth such as celite, or other pulverulent acid resisting mineral matter which need not have any reenforcing effect, the mineral matter being used basically to contribute hardness to the composition.
The asbestos used by me will be a good grade Canadian or other chrysotile asbestos such as Grade No. 5K (Canadian classification) of medium fiber length running up to inches in length, and averaging around inches in length. Very long length fiber is not required and simply presents greater mixing problems. A fiber length very much less would result in requiring more asbestos to be used than would be safe to avoid acid deterioration, which among other things, tends to swell the final composition when under acid'conditions.
In making the mixture, various procedures may be followed. The whole batch may be mixed at one time, or the mineral matter may be mixed with the asphaltic material and the asbestos mixed in subsequently. Or a mineral matter mix andanasbestosmixmaybothbemadeandthe two then mixed together. My preferred practice is to start with the bitumen in fluid condition, 1. e., above its ball and ring melt point, and then add and incorporate the mineral matter which will not be critical as to percentage, but should run to around 38%, since a better molding action is produced if the asphaltic ingredient con-. stitutes around 50% of the entire batch.
The asbestos is then wetted with water, or may be added dry to the mixer and water added to the mixer or its equivalent of steam inJected over a period of time. When wetting the ashestos, I have used with success water in the proportion of 25 pounds to 100 pounds of the asbestos. The lowest permissible moisture would be around by weight and if equal parts asbestos and moisture were used. the proceeding would be unsatisfactory.
The result in either event is to bring the temperature of the bitumen down during the initial mixing of the asbestos into thebatoh. However, the water serves its purpose during the initial portion of the mixing and heat applied to the mixer will be used to bring the temperature therein above the boiling point of water and preferably considerably higher before the end of the operation. The heat does not injure the asbestos and the great fluidity of the binder prevents too much pulverizing of the asbestos. I have finished the initial mixing in a two stage process as hereinafter noted, at a temperature, of 325 1''. for the last 5 minutes.
Before the mixing is completed, byone practice, I remove the material from the initial mixer and run it through an extrusion type of mixer, with additional heat applied, so as to extrude the material in a bar, permitting cutting off sections which when of a given length willhave a definite weight suitable for a mold charge for molding a storage battery container therefrom.
The amount of asbestos to use will'be not more than around 12 to 13%, and not less than around 7%, otherwise either the box will not stand up if the asbestos is more or will not be stron enough to satisfy requirements, if it" is less.
The lower percentage range will require-an asj bestos selected for quite long fiber length.
The molding operation is carried outinlthe normal manner for hot molding of storage battery composition containers and the result is to produce a box with a glossy and smooth'exterior which is highly satisfactory as a storage battery container.
The individual asbestos fibers will be-separated ln the mixture by films of the asphaltic inaterial, and surprising y. the strength is' fully as a result of the molding operation which requires a long fiow to form the battery partitions. Furthermore acid proof sprays such as are used in the organic fiber composition cases. e. 8-. acid resistant resins. are more eflective'as a sealer 4 of the surface of the container. a necessity, however, as tests on batteries in ordinary use, have shown no tendency to swell under influence of the electrolyte of the battery.
On a factory run using 48% storage battery case asphalt, 36% talc and 5% coal dust (as the bituminous and mineral ingredients), and 11% Canadian asbestos mixed in the presence of the amount of water above specified almost to completion and then given one pass through a Watson extrusion type mixer, gave a box upon molding which has a tensile strength of 1380 pounds per square inch, and an elongation of 81%. The pendulum crack test and acid absorption test on the finished product before spray coating ran about the same as the present day organic fiber asphalt composition cases of best standard. By using a vinylite resin spray, the acid absorption on two days exposure of the asbestos case was cut down to .06%, as compared to an absorption of 17% in the standard composition case when sprayed alike and contemporaneously tested.
I have illustrated a storage battery container in the drawings in which the view shows the case I having partitions 2 to create cells I for reception of packs of battery plates. The depth of flow required to mold such a product is apparent from its shape. I have shown a portion broken out of one of the partitions to indicate the coating 4, which preferably covers the inside of the case throughout.
Having thus described my invention, what I claim as new and desire to secure by Letters Patent is:
1. A storage battery container having a monolithic structure formed of hard asphaltic binder, finely divided acid resistant mineral matter, and chrysotile asbestos fiber in an amount of between around 7% to around 13% of the mass, the said finely divided acid resistant mineral matter and the said chrysotile asbestos fiber making up around 50% by weight of the mass.
. 2. A hot molding composition for the purpose describedconsisting of asphalt of the type employed for storage battery containers around 50% of the mass, chrysotile asbestos from around 'l'fijo around 13%, and the balance finely divided mineral matter, theasbestos having. a surface coatingon the individual fiber of the type obtained by hot mixing in the presence of H20. -3. A storage battery container having a monolithic structure and formed by molding from a composition consisting of substantially 48% hard asphalt, substantially 36% talc, substantially 5% coal..dust, and substantially 11% Canadian ashaving an initial fiber length of substantially in. to in.
4. The method of making a storage battery box "composition which consists in mixing asphaltic Ibinder', mineral matter and from 7% to 13% chrysotile asbestos to make a hot molding composition, the admixing of the asbestos with the binder being carried on in the presence of an Sealing is not 3 liquid, adding substantially 11 parts 0! a non- REFERENCES CITED acid'resistant asbesms having an initial The following references are of record in the length of substantially a, in. to in., along with file of this t substantially 10% to 50% of water based on the TEN weight of the asbestos, and mixing in the wet- 5 UNITED STATES PA ted asbestos as rapidly as possible under con- Number Name Date ditions to produce evaporation of the water, and ig gz 3g 325x13}? mix at a temperature substan 1:610:765 German Dec. 14: 1926 l0 1,755,500 Chamberlain Apr. 22, 1930 R. Luk ns 2,054,285 Foster Sept. 15, 1936

Claims (1)

1. A STORAGE BATTERY CONTAINER HAVING A MONOLITHIC STRUCTURE FORMED OF HARD ASPHALTIC BINDER, FINELY DIVIDED ACID RESISTANT MINERAL MATTER, AND CHRYSOTILE ASBESTOS FIBER IN AN AMOUNT OF BETWEEN AROUND 7% TO AROUND 13% OF THE MASS, THE SAID FINELY DIVIDED ACID RESISTANT MINERAL MATTER AND THE SAID CHRYSOTILE ASBESTOS FIBER MAKING UP AROUND 50% BY WEIGHT OF THE MASS.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2923638A (en) * 1956-05-14 1960-02-02 Monsanto Chemicals Asphalt adhesive composition
US9681652B2 (en) 2014-02-23 2017-06-20 Trece, Inc. Clasp hanger

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1166166A (en) * 1913-10-20 1915-12-28 James C Woodley Process of manufacturing a fibrous composition.
US1556703A (en) * 1923-01-04 1925-10-13 Richardson Co Process of fibrating asphalt
US1610765A (en) * 1924-09-06 1926-12-14 Louis Germain Jr Process of producing acid-resisting and heat-resisting articles
US1755500A (en) * 1925-09-25 1930-04-22 Gould Storage Battery Co Battery-box-container composition and method of making same
US1771643A (en) * 1925-08-28 1930-07-29 Richardson Co Fibrating process
US2054285A (en) * 1933-08-03 1936-09-15 Foster Benjamin Plastic composition

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1166166A (en) * 1913-10-20 1915-12-28 James C Woodley Process of manufacturing a fibrous composition.
US1556703A (en) * 1923-01-04 1925-10-13 Richardson Co Process of fibrating asphalt
US1610765A (en) * 1924-09-06 1926-12-14 Louis Germain Jr Process of producing acid-resisting and heat-resisting articles
US1771643A (en) * 1925-08-28 1930-07-29 Richardson Co Fibrating process
US1755500A (en) * 1925-09-25 1930-04-22 Gould Storage Battery Co Battery-box-container composition and method of making same
US2054285A (en) * 1933-08-03 1936-09-15 Foster Benjamin Plastic composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2923638A (en) * 1956-05-14 1960-02-02 Monsanto Chemicals Asphalt adhesive composition
US9681652B2 (en) 2014-02-23 2017-06-20 Trece, Inc. Clasp hanger

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