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Publication numberUS2837724 A
Publication typeGrant
Publication dateJun 3, 1958
Filing dateDec 29, 1953
Priority dateDec 29, 1953
Publication numberUS 2837724 A, US 2837724A, US-A-2837724, US2837724 A, US2837724A
InventorsCook Clinton D
Original AssigneeGen Electric
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Transformer with improved dielectric liquid
US 2837724 A
Abstract  available in
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Claims  available in
Description  (OCR text may contain errors)

June 3, 1958 c. D. COOK 2,837,724


Vt., assignor to General Electric Company,

This invention relates to a new dielectric liquid and particularly to an improved transformer utilizing the dielectric liquid.

Many large power transformers are cooled by a dielectric liquid such as a high boiling petroleum fraction or the halogenated aromatic compounds known as askarels. A dielectric liquid suitable for use as a transformer cooling agent should have high dielectric strength, a low percent power factor, and good resistance to a high impulse voltage. A satisfactory liquid must not only have a low percent power factor at the time it is placed in use but must retain this property by way of offering resistance to oxidation over a long period of time. An improvement in the dielectric liquid used for cooling is quickly reflected in an improved transformer since the same transformer may have a higher kva. rating if the dielectric liquid is improved.

It is an object of the present invention to provide an improved transformer characterized by a dielectric cooling liquid possessing very good resistance to oxidation.

It is another object of this invention to provide a dielectric liquid in which the condensation of diphenyl and tertiary alkyl groups confers resistance to oxidation and excellent dielectric properties.

The above and other objects are accomplished in accordance with this invention by incorporating in a transformer a dielectric fluid consisting of monotertiary alkyl diphenyl or methyldiphenyl isomers in which the alkyl groups contain from 48 carbon atoms.

The drawing is a cross-sectional view of a transformer constructed in accordance with this invention. A liquid tight tank has a cover 11 which may be sealed in airtight engagement with the tank. Mounted within the tank is a magnetic core 12 on which is wound a plurality of coils 13 constituting the primary and windings of the transformer. Terminals 14 and 15 extend through the cover 11 of the device.

The core and coils 12 and 13 are immersed in a dielectric liquid 16 which is an alkylated diphenyl or methyldiphenyl in which the alkyl group has a tertiary carbon atom and a total of from 4-8 carbon atoms. Where the compound used is diphenyl rather than methyldiphenyl, the dielectric liquid consists of three monotertiary alkyl isomers. In the case of methyldiphenyl compounds the mixture consists of a larger number of monotertiary alkyl isomers since the methylated diphenyl itself consists of a mixture of three isomers.

In preparing the dielectric fluids of this invention, di-

. phenyl or methyl diphenyl is subjected to a Friedel-Crafts condensation with a tertiary alkyl compound containing 4-8 carbon atoms and a fraction is then separated containing the monoalkyl derivatives from the unreacted starting products and the polyalkyl derivatives which are also present to some extent in the final reaction mixture. Of the tertiary alkyl compounds falling within the class described, I prefer to use tertiary butyl compounds first and tertiary arnyl compounds second. While these may secondary ICC be alcohols, halides, and other types of Friedel-Craits reactants, I find the most convenient tertiary alkyl compounds to use are the chlorides. In order to inhibit the formation of polytertiary alkyl compounds, it is desirable to have the diphenyl present in the reaction mixture in excess. This is shown in the following examples which are representative of means for producing the dielectric liquids of'this invention.

Example 1 Diphenyl (512 grams) is added to t-amyl chloride (267 grams) and the mixture is brought to a temperature of C. in a reflux apparatus. While maintaining this temperature aluminum chloride (30 grams) is slowly added while agitating the mixture. The reaction is complete in about 2 hours. After 2 /2 hours of reacting, the mixture is treated with 25 grams of fullers earth after which it is filtered and distilled. The fraction boiling between 300 C. and 375 C. contains the desired mon tertiary arnyl diphenyls.

Example 2 Diphenyl (77 grams) is mixedwith t-butyl alcohol (40 grams) and the mixture is heated to 80 C. after which anhydrous aluminum chloride (34 grams) is slowly added with stirring. After reacting for two hours the mixture is extracted with two 100 ml, portions of aqueous hydrochloric acid. The mixture is then washed three times with water, dried and distilled. The fraction boiling between 300 C. and 330 C. contains the monotertiary butyl diphenyl isomers of this invention.

Example 3 Diphenyl (1010 grams) is mixed with t-butyl chloride (350 grams) and the temperature of the mixture is raised to 50 C. in a reflux apparatus. Aluminum chloride 60 grams is slowly added while the mixture is agitated and the reaction is allowed to continue for 4 hours. It is then extracted twice with 1000 ml. portions of aqueous hydrochloric acid after which it is Washed four times with water, dried, and distilled. As in the case of Example 2, the fraction boiling between 300 C. and 330 G. contains the desired monotertiary butyl diphenyl isomers.

Example 4 Methyl diphenyl (50 grams) is added to diisobutylene (50 grams) and the mixture is brought to a temperature of C. Aluminum chloride (25 grams) is slowly added with stirring and the reaction is allowed to continue for 1%. hours. The mixture is then treated with 20 grams of fullers earth after which it is filtered and distilled. The fraction boiling between 300 C. and 400 C. is the desired mixture of monotertiary octyl methyl diphenyl isomers.

The dielectric liquids of this invention have a sixty cycle dielectric strength of between 50 and 55 kilovolts. Their impulse strength in a test of point to /2 sphere 1.5/40 negative wave varies from 214 kilovolts to 292 kilovolts with gap widths between /2 and one inch.

The dielectric liquids of this invention are very resistant to oxidation. They may be readily distilled at atmospheric pressure without undergoing any decomposition and at normal transformer operating temperatures they operate without sludging or discoloring over very long periods of time.

While the present invention has been described with reference to particular embodiments thereof, it will be understood that numerous modifications may be made by those skilled in the art without actually departing from the invention.

the true spirit and scope of the invention.

What I claim as new and Patent of the UnitedStates is:

1. A transformer comprising a liquid-tight tank, a magnetic core positioned in said tank, a plurality of windings on said core,and a dielectric liquid surrounding said core and coils consisting of a mixture of compounds having the formula in which R is a tertiary alkyl group having 4 to 8 carbon atoms and is attached to either ring and R is selected from the group consisting of hydrogen and CH and is attached to either ring.

2. A transformer comprising a liquid-tight tank, a magnetic core positionedin said tank, a plurality of windings on said core, and a dielectric fluid consisting of monotertiary butyl diphenyl isomers surrounding said core.

desire to secure by Letters 3. A transformer comprising a liquid-tight tank, a magnetic core positioned in said tank, a plurality of'windings on said core, and a Zdielectric fiuid consisting of monotertiary amyl diphenyl isomers surrounding said core.

I References Cited in thefrfile of this patent UNITED STATES PATENTS 7 OTHER REFERENCES Grosse et al.: Chem. Abs., vol. 33 (1939), col. 21123.

Rothstein et al.: Chem. Abs., vol. 44 (1950), col. 1449g.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US1878509 *Jul 12, 1928Sep 20, 1932Ig Farbenindustrie AgInsulating oil
US2172391 *Jun 29, 1936Sep 12, 1939Monsanto ChemicalsSubstituted diphenyl compositions
US2433020 *Aug 14, 1944Dec 23, 1947Standard Oil CoCatalytic alkylation of aromatic hydrocarbons by paraffins
US2572808 *Sep 18, 1948Oct 23, 1951Monsanto ChemicalsDielectric with n, n'-1-3 dimorpholino isopropanol as scavenger
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3108153 *Aug 21, 1959Oct 22, 1963Anaconda Wire & Cable CoHigh voltage electrical insulation including gassing inhibitor
US3145258 *Aug 21, 1959Aug 18, 1964Anaconda Wire & Cable CoTreated insulation impregnant for high voltage electrical cable
US4108789 *Jun 14, 1977Aug 22, 1978Rhone-Poulenc IndustriesDielectric compositions containing benzyl esters
US4119555 *Jun 8, 1977Oct 10, 1978Rhone-Poulenc IndustriesDielectric compositions comprising polychlorobenzene-alkyl terphenyl mixtures
US4177156 *Mar 10, 1978Dec 4, 1979Rhone-Poulenc IndustriesDielectric compositions comprising mixtures of polychlorinated benzenes and alkylaromatic hydrocarbons
US4368343 *Sep 18, 1980Jan 11, 1983Kotlyarevsky Izrail LProcess for producing high-vacuum oils
DE2726015A1 *Jun 8, 1977Dec 22, 1977Rhone Poulenc IndNeue fluessige dielektrika
WO1982000103A1 *Apr 15, 1981Jan 21, 1982Sun Oil Co PennsylvaniaSec-butylbiphenyl composition and process for preparing the same
U.S. Classification336/58, 585/459, 585/6.3, 585/25, 585/469
International ClassificationH01F27/10, H01B3/18, H01F27/12, H01B3/22
Cooperative ClassificationH01B3/22, H01F27/125
European ClassificationH01B3/22, H01F27/12A