NO133949B - - Google Patents

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Publication number
NO133949B
NO133949B NO2900/73A NO290073A NO133949B NO 133949 B NO133949 B NO 133949B NO 2900/73 A NO2900/73 A NO 2900/73A NO 290073 A NO290073 A NO 290073A NO 133949 B NO133949 B NO 133949B
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Prior art keywords
ester
mixture
weight
capacitors
hydrocarbon
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NO2900/73A
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Norwegian (no)
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NO133949C (en
Inventor
L Mandelcorn
T W Dakin
R L Miller
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Westinghouse Electric Corp
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Publication of NO133949B publication Critical patent/NO133949B/no
Publication of NO133949C publication Critical patent/NO133949C/no

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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G4/00Fixed capacitors; Processes of their manufacture
    • H01G4/002Details
    • H01G4/018Dielectrics
    • H01G4/20Dielectrics using combinations of dielectrics from more than one of groups H01G4/02 - H01G4/06
    • H01G4/22Dielectrics using combinations of dielectrics from more than one of groups H01G4/02 - H01G4/06 impregnated
    • H01G4/221Dielectrics using combinations of dielectrics from more than one of groups H01G4/02 - H01G4/06 impregnated characterised by the composition of the impregnant
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/20Insulators 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
    • C10M2203/022Well-defined aliphatic compounds saturated
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
    • C10M2203/024Well-defined aliphatic compounds unsaturated
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/04Well-defined cycloaliphatic compounds
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/06Well-defined aromatic compounds
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/026Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/044Cyclic ethers having four or more ring atoms, e.g. furans, dioxolanes
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/08Aldehydes; Ketones
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/281Esters of (cyclo)aliphatic monocarboxylic acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/282Esters of (cyclo)aliphatic oolycarboxylic acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/283Esters of polyhydroxy compounds
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/284Esters of aromatic monocarboxylic acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/285Esters of aromatic polycarboxylic acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/286Esters of polymerised unsaturated acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/34Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/18Containing nitrogen-to-nitrogen bonds, e.g. hydrazine
    • C10M2215/182Azo compounds
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/14Electric or magnetic purposes
    • C10N2040/16Dielectric; Insulating oil or insulators
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/14Electric or magnetic purposes
    • C10N2040/17Electric or magnetic purposes for electric contacts

Description

Den foreliggende oppfinnelse vedrører anvendelse av visse ester/hydrokarbon- ellér/ester/eterblandinger som dielektrJ.sk fluidum. The present invention relates to the use of certain ester/hydrocarbon or ester/ether mixtures as dielectric fluid.

Dielektriske fluider anvendes i kondensatorer, transfor-matorer, koaksialkabler og andre typer elektriske apparater for å utestenge gasser fra apparatets isolerende del og derved frembringe isolasjon som tåler høyere spenning. Dielectric fluids are used in capacitors, transformers, coaxial cables and other types of electrical devices to exclude gases from the device's insulating part and thereby produce insulation that can withstand higher voltages.

Et godt dielektrisk fluidum bør ha høy elektrisk fasthet A good dielectric fluid should have a high electrical resistance

og være billig samt fortrinnsvis ha brannmotstandsevne. Det bør være lettvint å rense for å oppnå lav ledningsevne eller lav tapsfaktor. Dersom det anvendes i kondensatorer, bør det ha relativt høy dielektrisitetskonstant og bør kunne impregnere kondensatorens dielektriske sperresjikt. Det bør ha gode koronaegenskaper, særlig dersom det anvendes i kondensatorer. Gode koronaegenskaper omfatter (ved delvis utladning) høye korona start- og slukkespenninger i et forsøk hvor spenningen økes til -korona setter inn og deretter reduseres. Videre bør sterk "korona (som kan opptre sporadisk i drift) ikke frembringe per-manent ødeleggelse, såsom vedvarende blærer, noe som ville redusere korona slukke- og nystartspenningene betydelig. Det dielektriske fluidum bør bibeholde dets. gode elektriske egenskaper and be cheap and preferably have fire resistance. It should be easy to clean to achieve low conductivity or low loss factor. If it is used in capacitors, it should have a relatively high dielectric constant and should be able to impregnate the capacitor's dielectric barrier layer. It should have good corona properties, especially if it is used in capacitors. Good corona properties include (in case of partial discharge) high corona start-up and extinguishing voltages in an experiment where the voltage is increased until -corona sets in and then reduced. Furthermore, strong "corona" (which may occur sporadically in operation) should not produce permanent damage, such as persistent blistering, which would significantly reduce the corona quench and restart voltages. The dielectric fluid should retain its good electrical properties

..<.>i ..<.>i

ved høye "temperaturer i der._dielektriske og metalliske komponenter at high "temperatures in there._dielectric and metallic components

i utstyret. Det bør ikke væire for flyktig, idet flyktige væsker er vanskelig å håndtere og fordamper hurtig ved bruk. Dersom et in the equipment. It should not be too volatile, as volatile liquids are difficult to handle and evaporate quickly during use. If a

dielektrisk fluidum går over i fast form', brister, det og taper /dielektrisk styrke. Derfor bør et godt dielektrisk fluidum ha -lav størkne--eller br i ste temperatur, slik at det kan anvendes ved lav temperatur. ,.; dielectric fluid turns into solid form', ruptures, it and loses /dielectric strength. Therefore, a good dielectric fluid should have a low solidification or breaking temperature, so that it can be used at a low temperature. ,.;

Forntiden er klorerte'difenylforbindelser, såsom triklor-difenyl (heretter benevnt "TCDP")-, mye brukt kommersielt som dielektriske fluider idet de gir et meget godt kompromiss jved- rørende mange ønskelige egenskaper. Men dielektriske fluider anvendes i store mengder, og det er alltid fare for tilfeldig tap eller lekkasje av fluidet. Mange av de klorerte forbindelser er ikke hurtig biologisk nedbrytbare, men holder seg i lange perioder og akkumuleres i næringskjeden. Til tross for deresønskelige egenskaper er det derfor mulig at klorerte difenyler snart kan bli helt forbudt for bruk som dielektriske fluider, eller slike forholdsregler kan bli involvert at bruken av dem vil bli meget kostbar. Idet hensynet til omgivelsene i de senere år er blitt et meget viktig forhold ved valg av dielektriske fluider, er det meget vanskelig å finne tilfredsstillende erstatninger for disse halogenerte dielektriske fluider. Currently, chlorinated diphenyl compounds, such as trichlorodiphenyl (hereafter referred to as "TCDP"), are widely used commercially as dielectric fluids, as they provide a very good compromise regarding many desirable properties. But dielectric fluids are used in large quantities, and there is always a risk of accidental loss or leakage of the fluid. Many of the chlorinated compounds are not rapidly biodegradable, but remain for long periods and accumulate in the food chain. Despite their desirable properties, it is therefore possible that chlorinated diphenyls may soon be completely prohibited for use as dielectric fluids, or such precautions may be involved that their use will become very expensive. Since consideration of the environment has become a very important factor in the selection of dielectric fluids in recent years, it is very difficult to find satisfactory replacements for these halogenated dielectric fluids.

Den blanding som ifølge oppfinnelsen anvendes som dielektrisk fluidum inneholder fra 20 til 95 vektsprosent av en ikke-halogenert organisk ester eller esterblanding som er væskeformig mellom -20 og 150°C og har en tapsfaktor på mindre enn 10% ved 100°C, og fra 5 til 80 vektsprosent av et ikke-halogenert aromatisk hydrokarbon eller en ikke-halogenert aromatisk eter som er løselig i esteren eller esterblandingen og har 2 eventuelt kondenserte benzenringer og kokepunkt på over 140°C samt en tapsfaktor på mindre enn 10% ved 100°C, fortrinnsvis også en i blanding løselig antioksydant i en mengde av 0,05 The mixture which according to the invention is used as a dielectric fluid contains from 20 to 95 percent by weight of a non-halogenated organic ester or ester mixture which is liquid between -20 and 150°C and has a loss factor of less than 10% at 100°C, and from 5 to 80% by weight of a non-halogenated aromatic hydrocarbon or a non-halogenated aromatic ether which is soluble in the ester or ester mixture and has 2 optionally fused benzene rings and a boiling point above 140°C and a loss factor of less than 10% at 100°C , preferably also a mixture-soluble antioxidant in an amount of 0.05

til 5,0 vektsprosent beregnet på blandingen av ester og hydrokarbon eller ester og eter, og/eller en i blandingen løselig hydrogenakseptor i en mengde av 0,3 til 3,0 vektsprosent beregnet av blandingen av ester og hydrokarbon eller ester og eter. to 5.0% by weight calculated on the mixture of ester and hydrocarbon or ester and ether, and/or a hydrogen acceptor soluble in the mixture in an amount of 0.3 to 3.0% by weight calculated on the mixture of ester and hydrocarbon or ester and ether.

En blanding av de ovenfor angitte estre og hydrokarboner eller etre er et meget godt dielektrisk fluidum, og, viktigst, den er biologisk nedbrytbar og utgjør ikke en potensiell fare for omgivelsene. I elektriske egenskaper, såsom elektrisk fasthet, taps- (eller kraft-) faktor, dielektrisitetskonstant samt koronaegenskaper, er den sammenliknbar med TCDP. Den kan lettvint renses for å oppnå en lav tapsfaktor. Dens koronaprodukter vedblir ikke som blærer. De foretrukne dielektriske fluider er TCDP overlegen i å bevare kondensatoren, noe som indikerer termisk stabilitet og inerthet overfor kondensatorkomponentene. Endelig er de dielektriske fluider som anvendes ifølge den foreliggende oppfinnelse billigere enn TCDP og kan anvendes sammen med de samme dielektriske materialer som anvendes i kondensatorer som inneholder TCDP. A mixture of the above esters and hydrocarbons or ethers is a very good dielectric fluid and, most importantly, it is biodegradable and does not pose a potential hazard to the environment. In electrical properties, such as electrical fastness, loss (or power) factor, dielectric constant as well as corona properties, it is comparable to TCDP. It can be easily cleaned to achieve a low loss factor. Its corona products do not persist as blisters. The preferred dielectric fluids are superior to TCDP in preserving the capacitor, indicating thermal stability and inertness to the capacitor components. Finally, the dielectric fluids used according to the present invention are cheaper than TCDP and can be used together with the same dielectric materials used in capacitors containing TCDP.

For at oppfinnelsen skal forstås bedre vil utførelsesformer av denne nå bli beskrevet ved hjelp av eksempler og under hen-visning til de medfølgende tegninger, hvori: Fig. 1 viser et isometrisk riss med et forstørret parti som viser konstruksjonen av en film-papir-film-kondensatorvikling. Fig. 2 viser et isometrisk riss med et parti delvis bort-skåret, hvilket viser viklingen ifølge fig. 1 anbrakt i en beholder til dannelse av en komplett kondensator. In order for the invention to be better understood, embodiments thereof will now be described by means of examples and with reference to the accompanying drawings, in which: Fig. 1 shows an isometric view with an enlarged part showing the construction of a film-paper-film -capacitor winding. Fig. 2 shows an isometric view with a part partially cut away, which shows the winding according to fig. 1 placed in a container to form a complete condenser.

Ifølge fig. 1 er to lag metallfolie 1 og 2 viklet med lag 3 av papir og lag 4 av plastfilm. Plastfilmen er fortrinnsvis polypropylen, idet denne gjør det mulig for kondensatoren å arbeide ved en høy KVAR (reaktiv kilovolt-ampere) pr. volum-enhet på grunn av dens høye elektriske styrke og lave tapsfaktor. Den nedbrytes heller ikke av de dielektriske fluider som anvendes ifølge-den foreliggende oppfinnelse selv under ekstreme driftsbetingelser. Andre plastfilmer, såsom HD-poly-etylen, vil også kunne anvendes. Ledninger 5 og 6 er koplet til foliene 1 og 2. En kondensatorvikling 7 er anbrakt i en beholder 8 og er impregnert med et dielektrisk fluidum 9 (se fig. 2). Ledningene 5 og 6 er koplet til koplingspunkter 10 -og 11. According to fig. 1 is two layers of metal foil 1 and 2 wrapped with layer 3 of paper and layer 4 of plastic film. The plastic film is preferably polypropylene, as this enables the condenser to work at a high KVAR (reactive kilovolt-ampere) per volume unit due to its high electrical strength and low loss factor. It is also not degraded by the dielectric fluids used according to the present invention even under extreme operating conditions. Other plastic films, such as HD polyethylene, can also be used. Wires 5 and 6 are connected to foils 1 and 2. A capacitor winding 7 is placed in a container 8 and is impregnated with a dielectric fluid 9 (see fig. 2). Wires 5 and 6 are connected to connection points 10 and 11.

De dielektriske fluider med de beste egenskaper inneholder en blanding med fra 75 til 90 vektsprosent av den organiske ester og fra 10 til 25 vektsprosent av det aromatiske hydrokarbon eller den aromatiske eter. The dielectric fluids with the best properties contain a mixture of from 75 to 90 percent by weight of the organic ester and from 10 to 25 percent by weight of the aromatic hydrocarbon or aromatic ether.

Den organiske ester inneholder fortrinnsvis en benzenring idet aromater har bedre koronamotstand og har bedre varmesta-bilitet. Enten esterens syredel eller dens basedel kan-være aromatisk. Ftalsyreestre synes å ha bedre egenskaper enn andre estre, -og særlig diisononylftalat (heretter benevnt "DINP") har utmerkete egenskaper. Andre egnete estre omfatter dibutyladipat, dietyladipat, diisodecyladipat, etylbenzoåt, n-butylbenzoat, isopropylbenzoat, isobutylbenzoat, n-propylbenzoat, etylkapronat, etylkaprylat, metylkaprylat, dietylmalonat, dimetylmalonat, di-etyloksalat, dibutylftalat, dietylftalat, dimetylftalat, dioktyl-ftalat, dietylsuccinat, butylvalerat etc. Blandinger av egnete estre kan utarbeides for å tilfredsstille temperaturkravene og kan også anvendes når de enkelte estre ikke tilfredsstiller temperaturkravene. The organic ester preferably contains a benzene ring, since aromatics have better corona resistance and have better thermal stability. Either the ester's acid part or its base part can be aromatic. Phthalic acid esters seem to have better properties than other esters, and especially diisononyl phthalate (hereinafter referred to as "DINP") has excellent properties. Other suitable esters include dibutyl adipate, diethyl adipate, diisodecyl adipate, ethyl benzoate, n-butyl benzoate, isopropyl benzoate, isobutyl benzoate, n-propyl benzoate, ethyl capronate, ethyl caprylate, methyl caprylate, diethyl malonate, dimethyl malonate, di-ethyl oxalate, dibutyl phthalate, diethyl phthalate, dimethyl phthalate, dioctyl phthalate, diethyl succinate, butyl valerate etc. Mixtures of suitable esters can be prepared to satisfy the temperature requirements and can also be used when the individual esters do not satisfy the temperature requirements.

Det aromatiske hydrokarbon eller den aromatiske eter er The aromatic hydrocarbon or the aromatic ether is

en forbindelse som er løselig i esteren, har en eller to benzenringer som kan være kondensert, har en tapsfaktor på mindre enn 10% ved 100°C. De bør ha lavt damptrykk, idet forbindelser med lavt kokepunkt er vanskelig å håndtere og kan fordampe i kondensatoren, og dets kokepunkt er over 14 0°C. Det anvendes to-ringsforbindelser idet disse har kokepunkt på over 140°C. Di-fenyloksyd (heretter benevnt DPO) foretrekkes idet dette har utmerkete elektriske egenskaper og ikke mykner polypropylenfilmen eller reagerer med denne i kondensatoren. Andre egnete aromatiske hydrokarboner eller etre omfatter acenaften, dibenzfuran, difenyl, difenylmetan, fluoren, naftalen, fenetol, etc. Blandinger av aromatiske hydrokarboner og/eller etre tas også i betraktning. a compound which is soluble in the ester, has one or two benzene rings which may be condensed, has a loss factor of less than 10% at 100°C. They should have a low vapor pressure, as compounds with a low boiling point are difficult to handle and can evaporate in the condenser, and its boiling point is above 14 0°C. Two-ring compounds are used as these have a boiling point of over 140°C. Diphenyl oxide (hereinafter referred to as DPO) is preferred as it has excellent electrical properties and does not soften the polypropylene film or react with it in the capacitor. Other suitable aromatic hydrocarbons or ethers include acenaphthene, dibenzfuran, diphenyl, diphenylmethane, fluorene, naphthalene, phenetol, etc. Mixtures of aromatic hydrocarbons and/or ethers are also contemplated.

Fortrinnsvis omfatter de dielektriske fluider også fra 0,05 til 5 vektsprosent (av esteren pluss hydrokarbonet eller eteren) av en antioksydant. Antioksydanten er en friradikalin-hibitor som er løselig i løsningen av esteren og hydrokarbonet eller eteren. Den hjelper til å holde tapsfaktoren lav i lang tid både for selve væsken og i kondensatoren. Den foretrukne mengde antioksydant er fra 0,1 til 3%, og en foretrukket antioksydant er di-tert-butyl-parakresol (heretter benevnt DTBPC) Preferably, the dielectric fluids also comprise from 0.05 to 5 percent by weight (of the ester plus the hydrocarbon or ether) of an antioxidant. The antioxidant is a free radical inhibitor which is soluble in the solution of the ester and the hydrocarbon or ether. It helps to keep the loss factor low for a long time both for the liquid itself and in the condenser. The preferred amount of antioxidant is from 0.1 to 3%, and a preferred antioxidant is di-tert-butyl-paracresol (hereinafter referred to as DTBPC)

som er funnet å virke meget godt. Andre egnete antioksydanter omfatter fenoler med formelen which has been found to work very well. Other suitable antioxidants include phenols of the formula

hvor R-gruppene typisk er hydrogen eller alkyl. Andre kjente antioksydanter som ikke øker det dielektriske fluidums tapsfaktor kan også anvendes. Blandinger av antioksydanter kan også tas i betraktning. where the R groups are typically hydrogen or alkyl. Other known antioxidants which do not increase the loss factor of the dielectric fluid can also be used. Mixtures of antioxidants can also be considered.

Det dielektriske fluidum omfatter fortrinnsvis også fra 0,3 til 3% (av esteren pluss hydrokarbonet eller eteren) av et koronabestandig tilsetningsmiddel for å øke det dielektriske fluidums bestandighet mot koronavirkning, ved å redusere tiden som kreves for å ta seg opp igjen fra en overspenning som for-årsaker korona. Dette tilsetningsmiddel er en forbindelse som reagerer med og opptar hydrogen under utladningsbetingelser og som er løselig i løsningen av esteren og den aromatiske eter eller hydrokarbon. Det antas å virke ved å oppta hydrogen som dannes ved korona og minsker derved dannelse av blærer. Et foretrukket tilsetningsmiddel er g-metylantrakinon, idet dette er enkelt å håndtere og er stabilt. Andre egnete tilsetningsmidler omfatter azobenzen, antrakinon og andre stoffer som kan oppta hydrogen. Blandinger av.tilsetningsmidler kan også anvendes. The dielectric fluid preferably also comprises from 0.3 to 3% (of the ester plus the hydrocarbon or ether) of a corona resistant additive to increase the resistance of the dielectric fluid to corona, by reducing the time required to recover from a surge which causes corona. This additive is a compound which reacts with and takes up hydrogen under discharge conditions and which is soluble in the solution of the ester and the aromatic ether or hydrocarbon. It is believed to work by absorbing hydrogen that is formed at the corona and thereby reduces the formation of blisters. A preferred additive is g-methylanthraquinone, as this is easy to handle and is stable. Other suitable additives include azobenzene, anthraquinone and other substances that can take up hydrogen. Mixtures of additives can also be used.

Oppfinnelsen vil nå bli beskrevet ved hjelp av de etter-følgende eksempler. The invention will now be described using the following examples.

Eksempel 1 Example 1

En blanding civ 80% DINP - 20% DPO ble fremstilt, og atskillige av dens egenskaper ble sammenliknet med egenskapene hos TCDP og mineralolje: A mixture civ 80% DINP - 20% DPO was prepared and several of its properties were compared with those of TCDP and mineral oil:

De ovenfor viste data viser at DINP-DPO-blandingen har tilfredsstillende egenskaper for kondensatorfremstilling (dvs. lav nok viskositet og lavt nok damptrykk og høyt nok flammepunkt) og kondensatorytelse, noe som vil bli vist mer fullstendig i de etterfølgende eksempler. Idet flammepunktet er det samme som for mineralolje., bør det tas tilsvarende forholdsregler for denne The above data show that the DINP-DPO blend has satisfactory characteristics for capacitor fabrication (ie, low enough viscosity and low enough vapor pressure and high enough flash point) and capacitor performance, which will be shown more fully in the following examples. As the flash point is the same as for mineral oil, corresponding precautions should be taken for this

blanding som de som er utviklet og akseptert for mineralolje. mixture as those developed and accepted for mineral oil.

Eksempel 2 Example 2

Det ble fremstilt små forsøkskondensatorer som hver inneholdt en vikling av en flatet rull av ark av 6 mikron aluminiumfolie, 12,5 mikron polypropylen, 13 mikron papir med tetthet 0,7, 12,5 mikron polypropylen, 6 mikron aluminiumfolie, 12,5 mikron polypropylen, 13 mikron papir samt 12,5 mikron polypropylen. Disse viklinger var omtrent 76,2 mm høye og 50,8 mm brede og Small experimental capacitors were made, each containing a winding of a flattened roll of sheets of 6 micron aluminum foil, 12.5 micron polypropylene, 13 micron paper of density 0.7, 12.5 micron polypropylene, 6 micron aluminum foil, 12.5 micron polypropylene, 13 micron paper and 12.5 micron polypropylene. These windings were approximately 76.2 mm high and 50.8 mm wide and

9,5 mm tykke og hadde kapitans på omtrent 0,3 u F. Noen kondensatorer ble impregnert med DINP og noen med 80% DINP - 20% DPO. Behandlingen ble foretatt ifølge fremgangsmåter som er kjent og anvendt av fagfolk på området. Impregneringen ble foretatt ved å tilsette det dielektriske fluidum under vakuum,øking av trykket til atmosfæretrykk og deretter utførelse av en vakuum-trykksyklus atskillige ganger. Enheten som var impregnert med 80% DINP - 20% DPO behøvde færre slike sykluser for å bli impregnert enn de som var impregnert med DINP. 9.5 mm thick and had a capacitance of about 0.3 u F. Some capacitors were impregnated with DINP and some with 80% DINP - 20% DPO. The treatment was carried out according to methods that are known and used by professionals in the field. The impregnation was carried out by adding the dielectric fluid under vacuum, increasing the pressure to atmospheric pressure and then performing a vacuum-pressure cycle several times. The device impregnated with 80% DINP - 20% DPO required fewer such cycles to become impregnated than those impregnated with DINP.

Eksempel 3 Example 3

Kondensatorer ble fremstilt som ifølge eksempel 2, med 80% DINP - 20% DPO og med TCDP. Den etterfølgende tabell gir resul-tatene av dielektrisitetsforsøk for kondensatorene og omfatter ekstrapolerte data for mineraloljeimpregnerte kondensatorer. Capacitors were prepared as according to example 2, with 80% DINP - 20% DPO and with TCDP. The following table gives the results of dielectric tests for the capacitors and includes extrapolated data for mineral oil-impregnated capacitors.

Tabellen ovenfor viser at kondensatorer som er impregnert med DINP - DPO har dielektrisitetskonstanter og effektfaktorer som er sammenliknbare med kondensatorer impregnert med TCDP. Den viser også at mineralolje er et relativt dårlig impregneringsmiddel for slike kondensatorer idet denne gir lav korona-slukkespenning, noe som ville gi kondensatorene lav slukkespen-ning, samt lav gjennomsnittlig dielektrisitetskonstant. The table above shows that capacitors impregnated with DINP - DPO have dielectric constants and power factors comparable to capacitors impregnated with TCDP. It also shows that mineral oil is a relatively poor impregnating agent for such capacitors as it gives a low corona cut-off voltage, which would give the capacitors a low cut-off voltage, as well as a low average dielectric constant.

Eksempel 4 Example 4

Under anvendelse av kondensatorer som var fremstilte som ifølge eksempel 2, med forskjellige dielektriske fluider, ble koronaegenskapene målt. Den etterfølgende tabell angir resul-tatene. Using capacitors prepared as in Example 2, with different dielectric fluids, the corona properties were measured. The following table indicates the results.

Forsøket ovenfor betraktes for å være ytterst hardt når det gjelder de seks sekunder med kontinuerlig overspenning. Disse overspenninger på 5300 og 4300 volt er de høyeste som ventes ved kraftkondensatordrift, i henholdsvis serie- og shunt-kopling, for dielektrika med denne sammensetning, og de ville opptre i bare en brøkdel av en syklus (<L1/60 sekund) ved et-hvert tidspunkt. Dette forsøk viser, med stor sikkerhetsmargin, om et gitt dielektrikum vil ta seg opp fra virkningene av slike overspenninger. Tabellen viser at tilsetningen av DPO til DINP øker koronabestandigheten vesentlig. Antioksydanten DTBPC The above test is considered to be extremely harsh in terms of the six seconds of continuous overvoltage. These overvoltages of 5300 and 4300 volts are the highest expected in power capacitor operation, in series and shunt, respectively, for dielectrics of this composition, and would occur for only a fraction of a cycle (<L1/60 second) at a -every time. This experiment shows, with a large margin of safety, whether a given dielectric will recover from the effects of such overvoltages. The table shows that the addition of DPO to DINP significantly increases corona resistance. The antioxidant DTBPC

hadde ikke videre innvirkning på denne, men en hydrogenopp-taker, såsom B-metylantrakinon eller azobenzen bedret den ytterligere. had no further effect on this, but a hydrogen acceptor such as B-methylanthraquinone or azobenzene improved it further.

Eksempel 5 Example 5

Idet det ble anvendt kondensatorer som beskrevet i eksempel 2 impregnert med forskjellige dielektriske fluider, ble kondensatorenes levetid bestemt ved aldring ved 125°C med 1600 volt påtrykt spenning. Sluttpunktet for levetiden for kondensatoren ble betraktet å være nådd når tapsfaktoren øket til et nivå hvor ukontrollert termisk-forandring kan opptre i en stor kraftkondensator. Den etterfølgende tabell angir resul-tatene, hvor "relativ levetid" er forholdet mellom kondensatorens levetid og levetid for kondensatoren impregnert med As capacitors as described in example 2 impregnated with different dielectric fluids were used, the life of the capacitors was determined by aging at 125°C with 1600 volts applied voltage. The end point of the life of the capacitor was considered to be reached when the loss factor increased to a level where uncontrolled thermal change can occur in a large power capacitor. The following table indicates the results, where "relative lifetime" is the ratio between the lifetime of the capacitor and the lifetime of the capacitor impregnated with

TCDP: TCDP:

De ovenfor angitte data indikerer at blandingene som anvendes ifølge den foreliggende oppfinnelse er særlig gode impregneringsmidler for film-papir-kondensatorer og hel-papir-kondensatorer, og at kondensatorer som er impregnert med slike blandinger inneholdende antioksydanter har langt lengre levetid enn kondensatorer som er impregnert med TCDP. Dataene indikerer at en driftslevetid på minst omtrent 40 år kan ventes for 150 KVAR kraftkondensatorer (med en forvarmertemperatur på 85°C i 10% av tiden) dersom det dielektriske fluidum er 80% DINP-20% DPO med 0,26% DTBPC. The above-mentioned data indicate that the mixtures used according to the present invention are particularly good impregnation agents for film-paper capacitors and all-paper capacitors, and that capacitors impregnated with such mixtures containing antioxidants have a much longer service life than capacitors that are impregnated with TCDP. The data indicate that a service life of at least approximately 40 years can be expected for 150 KVAR power capacitors (with a preheater temperature of 85°C for 10% of the time) if the dielectric fluid is 80% DINP-20% DPO with 0.26% DTBPC.

Eksempel 6 Example 6

Det ble fremstilt kondensatorer med 0,8 u F med to lag 12 mikron papir med tetthet 0,9 mellom aluminiumfo.lie. Kondensatorene ble impregnert med 80%DINP- 20% DPO.Effektfaktoren ble bestemt til 0,26% ved 85°C og 0,38% ved 125°C med 440 volt påtrykt, Koronabegynnelsesspenningene var over 800 volt. Disse kondensatorer kunne anvendes for belysningsballast, motorstart-ing, koromutatorer samt lavspennings-effektfaktorkorreksjoner. Capacitors of 0.8 µF were made with two layers of 12 micron paper with a density of 0.9 between aluminum foil. The capacitors were impregnated with 80% DINP- 20% DPO. The power factor was determined to be 0.26% at 85°C and 0.38% at 125°C with 440 volts applied, Corona onset voltages were over 800 volts. These capacitors could be used for lighting ballasts, motor starting, coromutators as well as low voltage power factor corrections.

Eksempel 7 Example 7

Det ble fremstilt enliters volumer av 80% DINP - 20% DPO og 8u% DINP - 20% DPO som inneholdt 0,15% DTBPC antioksydant. Begge væsker ble eksponert for omgivende luft ved 100°C. Etter fire døgn hadde tapsfaktoren for væsken som ikke inneholdt antioksydanten øket til mer enn 10%. Etter to uker hadde tapsfaktoren for væsken som inneholdt antioksydanten øket mindre enn 1%. One liter volumes of 80% DINP - 20% DPO and 8u% DINP - 20% DPO containing 0.15% DTBPC antioxidant were prepared. Both liquids were exposed to ambient air at 100°C. After four days, the loss factor for the liquid that did not contain the antioxidant had increased to more than 10%. After two weeks, the loss factor for the liquid containing the antioxidant had increased by less than 1%.

Eksempel 8 Example 8

Det ble fremstilt forsøkskondensatorseksjoner ifølge eksempel 5, hvor det ble anvendt 0,15% DTBPC, noen med fortinnete kobberledninger og andre med aluminiumledninger, og anbrakt i stålbeholdere som vist i fig. 2. Kondensatorene ble drevet ved 115°C ved 1600 volt. Begge grupper hadde samme driftsstabilitet uten skadelige effekter som følge av nærvær av kobber. Kobber katalyserer nedbrytingen av de organiske forbindelser med en høy prosentandel hydrogen, såsom dette impregneringsmiddel, men antioksydanten antas å ha inhibert denne effekt. Experimental capacitor sections were produced according to example 5, where 0.15% DTBPC was used, some with tinned copper wires and others with aluminum wires, and placed in steel containers as shown in fig. 2. The capacitors were operated at 115°C at 1600 volts. Both groups had the same operating stability without harmful effects due to the presence of copper. Copper catalyzes the breakdown of the organic compounds with a high percentage of hydrogen, such as this impregnating agent, but the antioxidant is believed to have inhibited this effect.

Claims (2)

1. Anvendelse av en blanding av fra 20 til 95 vektsprosent av en ikke-halogenert organisk ester eller esterblanding som er væskeformig mellom -20 og +150°C og har en tapsfaktor på mindre enn 10% ved 100°C, og fra 5 til 80 vektsprosent av minst et ikke-halogenert aromatisk hydrokarbon eller en ikke-halogenert aromatisk eter som er løselig i esteren eller esterblandingen og har 2 eventuelt kondenserte benzenringer og kokepunkt på over 140°C samt en tapsfaktor på mindre enn 10% ved 100°C, fortrinnsvis også en i blandingen løselig antioksydant i en mengde av 0,05 til 5 vektsprosent beregnet på blandingen av ester og hydrokarbon eller ester og eter, og/eller en i blandingen løse-lig hydrogenakseptor i en mengde av 0,3 til 3,0 vektsprosent beregnet av blandingen av ester og hydrokarbon eller ester og eter - som dielektrisk fluidum.1. Use of a mixture of from 20 to 95% by weight of a non-halogenated organic ester or ester mixture which is liquid between -20 and +150°C and has a loss factor of less than 10% at 100°C, and from 5 to 80% by weight of at least one non-halogenated aromatic hydrocarbon or a non-halogenated aromatic ether which is soluble in the ester or ester mixture and has 2 possibly condensed benzene rings and a boiling point of over 140°C and a loss factor of less than 10% at 100°C, preferably also an antioxidant soluble in the mixture in an amount of 0.05 to 5% by weight calculated on the mixture of ester and hydrocarbon or ester and ether, and/or a hydrogen acceptor soluble in the mixture in an amount of 0.3 to 3.0 weight percent calculated from the mixture of ester and hydrocarbon or ester and ether - as dielectric fluid. 2. Anvendelse i samsvar med krav 1 av en blanding hvor esteren forekommer i en mengde av- fra 7 5 til 90 vektsprosent og det aro matiske hydrokarbon eller den aromatiske eter forekommer i en mengde på fra 10 til 25 vektsprosent.2. Use in accordance with claim 1 of a mixture where the ester occurs in an amount of from 75 to 90 percent by weight and the aro matic hydrocarbon or the aromatic ether occurs in an amount of from 10 to 25 percent by weight.
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US4290926A (en) 1976-03-24 1981-09-22 General Electric Company Non-halogenated impregnant for capacitors comprising an aromatic carboxylic acid ester and an alkene
US4054937A (en) * 1976-04-28 1977-10-18 Westinghouse Electric Corporation Capacitor
US4266264A (en) * 1977-06-24 1981-05-05 Westinghouse Electric Corp. Meta isopropyl biphenyl insulated electrical apparatus
US4121275A (en) 1977-06-27 1978-10-17 Sprague Electric Company Ester dielectric fluid containing tert-butyl anthraquinone
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