US2594872A - Stabilization of halogenated hydrocarbons - Google Patents
Stabilization of halogenated hydrocarbons Download PDFInfo
- Publication number
- US2594872A US2594872A US601676A US60167645A US2594872A US 2594872 A US2594872 A US 2594872A US 601676 A US601676 A US 601676A US 60167645 A US60167645 A US 60167645A US 2594872 A US2594872 A US 2594872A
- Authority
- US
- United States
- Prior art keywords
- aluminum
- dielectric
- liquid
- compound
- resistivity
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 150000008282 halocarbons Chemical class 0.000 title description 8
- 230000006641 stabilisation Effects 0.000 title description 4
- 238000011105 stabilization Methods 0.000 title description 4
- 239000007788 liquid Substances 0.000 description 26
- 229910052782 aluminium Inorganic materials 0.000 description 21
- 239000003990 capacitor Substances 0.000 description 19
- 150000001875 compounds Chemical class 0.000 description 19
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 18
- -1 halogenated aryl hydrocarbon Chemical class 0.000 description 17
- 239000000203 mixture Substances 0.000 description 17
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 12
- 230000006866 deterioration Effects 0.000 description 12
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 11
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 11
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 11
- 239000003381 stabilizer Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 10
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- 125000006850 spacer group Chemical group 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 230000032683 aging Effects 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 4
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 4
- 150000001491 aromatic compounds Chemical class 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 229910001570 bauxite Inorganic materials 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 125000006267 biphenyl group Chemical group 0.000 description 2
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 230000017525 heat dissipation Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 229920006389 polyphenyl polymer Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- PPKPKFIWDXDAGC-IHWYPQMZSA-N (z)-1,2-dichloroprop-1-ene Chemical compound C\C(Cl)=C\Cl PPKPKFIWDXDAGC-IHWYPQMZSA-N 0.000 description 1
- HYFLWBNQFMXCPA-UHFFFAOYSA-N 1-ethyl-2-methylbenzene Chemical compound CCC1=CC=CC=C1C HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- JSNUUPDHVXZNGO-UHFFFAOYSA-N [Cl].C1=CC=CC=2C(C3=CC=CC=C3C(C12)=O)=O Chemical compound [Cl].C1=CC=CC=2C(C3=CC=CC=C3C(C12)=O)=O JSNUUPDHVXZNGO-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 239000010431 corundum Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 229910001648 diaspore Inorganic materials 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229910001679 gibbsite Inorganic materials 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000006194 liquid suspension Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000002927 oxygen compounds Chemical class 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical class CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- HUAUNKAZQWMVFY-UHFFFAOYSA-M sodium;oxocalcium;hydroxide Chemical compound [OH-].[Na+].[Ca]=O HUAUNKAZQWMVFY-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/20—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances liquids, e.g. oils
- H01B3/24—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances liquids, e.g. oils containing halogen in the molecules, e.g. halogenated oils
Definitions
- the present invention relates to electrical devices, as, for example, transformers, capacitors, regulators, bushings, and the like, which contain liquid halogenated aromatic hydrocarbons as insulating and dielectric media.
- Insulating and dielectric compositions comprising halogenated aromatic compounds have many desirable properties. They are stable chemically under ordinary operating conditions. However, experience has shown that such compounds, and particularly the halogenated mononuclear compounds, are subject to some deterioration during use in electrical devices. Deterioration becomes evident by decrease of resistivity at elevated temperatures, say at 100 C. and upward. It is the object of my present invention to decrease or entirely avoid such deterioration.
- oxygenous compound I mean to include only inorganic compound of the oxide and hydroxide type.
- My invention comprises halogenated aryl hydrocarbon in combination with oxide, hydroxide, or other suitable oxygenous aluminum compound, including corundum, gibbsite, diaspore and bauxite; my invention includes also electrical devices containing such combination in operative relation to cooperating electrical conductors charged with different potentials.
- Fig. 1 illustrates a transformer provided with a foraminous receptacle containing a quantity of stabilizer
- Fig. 2 shows a modified structure in which the stabilizer is placed in a tubular side chamber
- Figs. 3 and 4 illustrate capacitors embodying my invention.
- a transformer comprising a core I and electrical windings 2, contained in a tank 3 and provided with external terminals 4, 5, as usual.
- the tank also contains a quantity 6 of insulatin liquid consisting wholly or in part of aromatic halogenated hydrocarbon.
- a foraminous receptacle 3 Suspended from the tank cover 1 is a foraminous receptacle 3 consisting of wire mesh, spun glass, cellulosio fabric, or other suitable material, and containing a quantity of suitable oxygenous compound of aluminum which functions as a stabilizer by its contact with the halogenated hydrocarbon.
- the oxygenous aluminum compound is contained in the tubular side chamber 9 which is in communication at both ends with the main tank.
- a slow circulation of the halogenated hydrocarbon liquid 6 occurs through the chamber 9 where the circulating liquid comes into contact with the aluminum compound.
- halogenated aromatic hydrocarbon liquid Approximately one-fourth pound of aluminum oxide, bauxite, or the like, is provided per gallon of halogenated aromatic hydrocarbon liquid. This amount of stabilizer (about 2 per cent by weight) is illustrative but not critical. Greater and lesser amounts have been found to be of practical utility.
- a selected aluminum compound may be heated to a temperature in the range of about 350 to 500 C. in order to remove all moisture and to produce a substantially dry solid.
- the aluminum compound preferably should be of a size retained by about 8 to 16 mesh. This size is not critical as material of 30 to mesh has been found to be of practical utility.
- special precautions are necessary to insure liquid flow over or through the stabilizer without the material being taken up in liquid suspension.
- the oxygenous aluminum compound is pressed into porous plates or cylinders through which the liquid flows. Rods which are hung in the liquid to obtain intimate contact may be used. Intimate contact between the stabilizer and the halogenated aromatic compound is an important requisite.
- the following example illustrates the efficiency of a retarder comprising an oxygenous aluminum in transformers containing trichlorbenzene as the cooling and dielectric medium.
- Commercial five kilowatt transformers (which will be referred to as the first set) were dried in the usual manner and then filled with trichlorbenzene.
- the resistivity of the trichlorbenzene decreased rapidly.
- the resistivity was 30 10 ohms-centimeter at 100 C.
- the dielectric strength was 40 kilovolts when tested at 25 C. using the method D-11'7 of the American Society for Testing Materials.
- the dielectric loss of the transformers of this first set averaged about two watts immediately after filling with trichlorbenzene. After one months operation at normal voltage, and under restricted. conditions of heat dissipation resulting in a liquid temperature of 80 C., the dielectric loss had risen to 15 watts.
- the transformers of this first set when operated under the described conditions, continued to rise in dielectric loss with continued operation and reached dielectric losses as high as 30 watts. The transformers of this set failed in approximately six months.
- Trichlorbenzene only x10 Trichlorbenzene with aluminum oxide- 3950 10 In the presence of aluminum hydroxide, the resistivity of trichlorbenzene is increased.
- Trichlorbenzene only 4.4X10 Trichlorbenzene with aluminum oxide 965x 10 entachlor ifi fi diphenyl with E aluminum hydroxide Original resistivity tested at 100 C 6, 300x10 6, 300Xl0 Tested after 1 week aging at 100 0.... 3,140 10, 200X10 Tested after 2 weeks aging at 100 C. 1,180 23, 500x10 Trichlor-
- my invention is applicable to mixtures of halogenated polynuclear and mononuclear hydrocarbons functioning as insulating or dielectric media.
- Such a liquid composition may consist, for example, of a solution of per cent chlordiphenyl (chlorinated to contain 60 per cent chlorine) and 40 per cent trichlorbenzene.
- the resistivity falls to approximately 450x10 ohms-centimeter when measured at 100 C. In'the presence of the resin-bonded, paper-laminated paper, the resistivity falls to approximately 60 1G ohms-centimeter. When, however, such a composition is in contact with aluminum oxide, the resistivity is maintained at a high value.
- the resistivities obtained are approximately 3500x10 and 2000 10 ohmscentimeter respectively.
- a composition used for the impregnation of capacitors consists by Weight of about parts of pentachlor and 25 parts of trichlorbenzene.
- the composition may contain about .5 per cent anthraquinone or one per cent monochlor anthraquinone, or one per cent of dichlor anthraqui-
- the resistivity drops from an initial value of about 2670 10 ohms centimeter to about 212x10 ohms-centimeter.
- AHOHM aluminum hydroxide
- the resistivity actually increases under the same conditions to 3690x10 ohms-centimeter. It is particularly desirable to maintain the resistivity of capacitors for the direct current field as high as possible.
- the oxygenous compound of aluminum such as aluminum oxide or hydroxide
- the material should be finely divided, preferably 30-60 mesh. I have found it desirable to pack the -material as with a vibrator. Because of its excellent heat conductivity, the presence of the oxygenous aluminum compound does not adversely affect the heat dissipation characteristics of the capacitor.
- Fig. 4 shows in cross-section a capacitor in which the capacitor rolls 10, H are contained in a casing l2.
- the dielectric paper spacer between the armatures is loaded with the finely divided oxygenous aluminum compound during the manufacture of the paper.
- the aluminum compound thus acts as a filler in the paper.
- Fig. 3 shows a capacitor assembly partly unrolled, the paper spacers charged with oxygenous compound of aluminum being indicated at l4, [5.
- the terminals I6, I? make contact with the armatures l8, l9. With either mode of application, I have found that the desired stabilization of the halogenated impregnant is obtained.
- chlorinated benzene and polyphenyl may be associated advantageously in an electric device with an oxygen compound of aluminum.
- alkyl derivatives include the methyl, ethyl, propyl benzenes, dimethyl benzene, methyl-ethyl benzene, and the like.
- An insulating and dielectric composition comprising, in combination, liquid halogenated aromatic hydrocarbon and a change of a compound selected from the class consisting of aluminum hydroxide and aluminum oxid sufficient in amount to prevent decrease of resistivity of said composition.
- An insulating and dielectric composition comprising in combination liquid chlorinated mononuclear hydrocarbon and a sufficient quantity of a compound selected from the class consisting of aluminum hydroxide and aluminum oxide to prevent substantial rise of power factor.
- An insulating medium consisting of trichlorbenzene and an effective quantity of a compound selected from the class consisting of aluminum hydroxide and aluminum oxide in contact therewith, to prevent material decrease of electrical conductivity at elevated temperature.
- An insulating and cooling composition consisting of a liquid mixture of trichlorbenzene and chlorinated diphenyl and about two per cent by weight of aluminum oxide in contact with said mixture.
- An electric device including in combination cooperating conductors normally charged with different potentials, insulating means therefor consisting of liquid halogenated aromatic hydrocarbon and a sufiicient quantity of a compound selected from the class consisting of aluminum hydroxide and aluminum oxide in contact with said halogenated hydrocarbon to prevent decrease of resistivity of said hydrocarbon.
- An electric capacitor including the combination of cooperating armatures a dielectric medium therehetween consisting of liquid chlorinated aromatic hydrocarbon and a quantity of a compound selected from the class consisting of aluminum hydroxide and aluminum oxide in contact with said chlorinated hydrocarbon.
- An electric capacitor comprising the combination of a container, capacitor elements disposed therein and comprising cooperating armatures, a dielectric paper spacer between said armatures and a dielectric impregnant consisting of halogenated aromatic hydrocarbon and a quantity of a compound selected from the class consisting of aluminum hydroxide and aluminum oxide in said container in contact with said hydrocarbon.
- An electric capacitor comprising the combination or" a container, capacitor elements disposed therein and comprising cooperating armatures, a dielectric paper spacer between said armatures and a dielectric impregnant consisting of a liquid chlorinated benzene compound and a quantity of a compound selected from the class consisting of aluminum hydroxide and aluminum oxide in said container in contact with said benzene compound.
- An electric capacitor comprising the combination of a container, capacitor elements disposed therein and comprising cooperating armatures, a dielectric paper spacer between said armatures and a dielectric impregnant consisting of a. liquid chlorinated diphenyl compound and a quantity of aluminum oxide in said container in contact with said diphenyl compound.
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Organic Insulating Materials (AREA)
- Fixed Capacitors And Capacitor Manufacturing Machines (AREA)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US601676A US2594872A (en) | 1945-06-26 | 1945-06-26 | Stabilization of halogenated hydrocarbons |
BE468719D BE468719A (enrdf_load_stackoverflow) | 1945-06-26 | 1946-10-24 | |
BE483471D BE483471A (enrdf_load_stackoverflow) | 1945-06-26 | 1948-06-25 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US601676A US2594872A (en) | 1945-06-26 | 1945-06-26 | Stabilization of halogenated hydrocarbons |
Publications (1)
Publication Number | Publication Date |
---|---|
US2594872A true US2594872A (en) | 1952-04-29 |
Family
ID=24408356
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US601676A Expired - Lifetime US2594872A (en) | 1945-06-26 | 1945-06-26 | Stabilization of halogenated hydrocarbons |
Country Status (2)
Country | Link |
---|---|
US (1) | US2594872A (enrdf_load_stackoverflow) |
BE (1) | BE468719A (enrdf_load_stackoverflow) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3214658A (en) * | 1962-12-03 | 1965-10-26 | Ohio Brass Co | Capacitor including aluminum silicate scavenger |
US3780206A (en) * | 1971-11-26 | 1973-12-18 | British Insulated Callenders | Electric cables |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1927112A (en) * | 1932-04-07 | 1933-09-19 | Howard W Cole | Container for collapsible tubes |
US1966163A (en) * | 1932-09-29 | 1934-07-10 | Gen Electric | Electric device and dielectric material therefor |
US1994302A (en) * | 1933-10-18 | 1935-03-12 | Gen Electric | Refining process |
US1994911A (en) * | 1933-02-15 | 1935-03-19 | Westinghouse Electric & Mfg Co | Corrosion-resisting product |
US2019339A (en) * | 1934-09-29 | 1935-10-29 | Gen Electric | Snuffer composition |
US2036274A (en) * | 1934-11-27 | 1936-04-07 | Westinghouse Electric & Mfg Co | Insulating liquid |
US2077429A (en) * | 1937-04-20 | G f mcmahon | ||
US2111414A (en) * | 1936-12-04 | 1938-03-15 | Gen Electric | Electrical insulating composition |
GB545500A (en) * | 1940-09-27 | 1942-05-29 | Donald Whittaker | Improvements in or relating to halogenated polythenes |
US2286744A (en) * | 1935-11-20 | 1942-06-16 | Leatherman Martin | Process of fireproofing |
US2391686A (en) * | 1938-08-31 | 1945-12-25 | Bell Telephone Labor Inc | Electrical condenser and dielectric element |
-
1945
- 1945-06-26 US US601676A patent/US2594872A/en not_active Expired - Lifetime
-
1946
- 1946-10-24 BE BE468719D patent/BE468719A/fr unknown
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2077429A (en) * | 1937-04-20 | G f mcmahon | ||
US1927112A (en) * | 1932-04-07 | 1933-09-19 | Howard W Cole | Container for collapsible tubes |
US1966163A (en) * | 1932-09-29 | 1934-07-10 | Gen Electric | Electric device and dielectric material therefor |
US1994911A (en) * | 1933-02-15 | 1935-03-19 | Westinghouse Electric & Mfg Co | Corrosion-resisting product |
US1994302A (en) * | 1933-10-18 | 1935-03-12 | Gen Electric | Refining process |
US2019339A (en) * | 1934-09-29 | 1935-10-29 | Gen Electric | Snuffer composition |
US2036274A (en) * | 1934-11-27 | 1936-04-07 | Westinghouse Electric & Mfg Co | Insulating liquid |
US2286744A (en) * | 1935-11-20 | 1942-06-16 | Leatherman Martin | Process of fireproofing |
US2111414A (en) * | 1936-12-04 | 1938-03-15 | Gen Electric | Electrical insulating composition |
US2391686A (en) * | 1938-08-31 | 1945-12-25 | Bell Telephone Labor Inc | Electrical condenser and dielectric element |
GB545500A (en) * | 1940-09-27 | 1942-05-29 | Donald Whittaker | Improvements in or relating to halogenated polythenes |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3214658A (en) * | 1962-12-03 | 1965-10-26 | Ohio Brass Co | Capacitor including aluminum silicate scavenger |
US3780206A (en) * | 1971-11-26 | 1973-12-18 | British Insulated Callenders | Electric cables |
Also Published As
Publication number | Publication date |
---|---|
BE468719A (enrdf_load_stackoverflow) | 1946-11-30 |
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