GB679539A - Improvements in electrostatic capacitors - Google Patents

Improvements in electrostatic capacitors

Info

Publication number
GB679539A
GB679539A GB20044/48A GB2004448A GB679539A GB 679539 A GB679539 A GB 679539A GB 20044/48 A GB20044/48 A GB 20044/48A GB 2004448 A GB2004448 A GB 2004448A GB 679539 A GB679539 A GB 679539A
Authority
GB
United Kingdom
Prior art keywords
glycol
resin
unsaturated
reacted
acids
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
Application number
GB20044/48A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Aerovox Corp
Original Assignee
Aerovox Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Aerovox Corp filed Critical Aerovox Corp
Publication of GB679539A publication Critical patent/GB679539A/en
Expired legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-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
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-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

Landscapes

  • Engineering & Computer Science (AREA)
  • Power Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Organic Insulating Materials (AREA)

Abstract

An electrostatic capacitor comprises electrodes separated by an interspacer impregnated with the solid, substantially insoluble and infusible copolymerization product of a poly-unsaturated alkyd resin initially reacted to an acid member below 150, alcoholised to reduce the acid number below 75 and acylated to render it devoid of free hydroxyl radicals, with a liquid copolymerizable monomer in the proportion of 20-70 per cent by weight of the composition. Saturated polyhydric alcohols which may be used for making the alkyd are ethylene glycol; 1,2-propylene glycol; isobutylene glycol; trimethylene glycol; 1,4-butylene glycol; phthalyl alcohol; glycerol; a -methyl-glycerol; pinacol; sorbitol; mannitol; erythritol; pentaerythritol; diethylene glycol; pentamethylene glycol; trethylene glycol; tetramethylene glycol; unsaturated polyhydric alcohols are vinyl glycol or the compound HOCH2CH=CHCH2OH. Suitable unsaturated acids are maleic, fumaric, itaconic, citraconic, acetylene dicarboxylic, glutaconic, methylene malonic, or mesaconic. Acids such as phthalic, succinic, adipic, azalic, sebacic or malonic may also be included. Monohydric alcohols or acids, saturated or unsaturated may be incorporated in the reaction mixture as modifying ingredients. Lists are given of suitable ingredients of this type. Acids suitable for the final acylation of the alcoholised alkyd are acetic, propionic, acrylic, methacrylic, oleic, cinnamic, benzoic or chloracetic. Suitable copolymerizable monomers are styrene; vinyl acetate; acrylonitrile; methyl, butyl, allyl, crotyl or methallyl acrylate, a -chloracrylate or methacrylate; glycol diacrylate; diallyl phthalate; diallyl, dimethallyl, divinyl, di-isoprophenyl or dicrotyl carbonate or other unsaturated alcohol polyesters of polybasic acids. The resin or resin mixture may be copolymerized by heat or light, preferably with peroxide catalysts, several of which are mentioned. Rate of polymerization may be increased by addition of activators, e.g. cobalt linoleate, cobalt naphthenate, cuprous oxide, trithanolamine or stannous chloride. An inhibitor such as tert.-butyl catechol, diphenylamine, or hydroquinone may be introduced to preclude premature polymerization. In examples: (1) ethylene glycol and maleic anhydride are reacted, the product reacted with methanol, and, after removal of excess methanol with acetic anhydride; (2) diethylene glycol and maleic anhydride are reacted, the product heated with n-propanol, excess of which is removed by distillation and the product esterified with acetic anhydride; (3) the methylated ethylene glycol maleate of example (1) is esterified with oleic acid; (4) phthalic anhydride, maleic anhydride and ethylene glycol are reacted together, the product treated with n-propanol and then with acetic anhydride; (5) is similar to (4) with hydroquinone present during the initial reaction. Capacitor sections may be impregnated, preferably after drying with the compositions of the invention. Vacuum and pressure may be used to aid impregnation. Excess resin may be removed by washing the sections with styrene. The sections may be encased preferably in a casing moulded from a resin similar to that used as dielectric in which case both resins may be cured at the same time (see Group V). The resin for the casing preferably contains no inhibitor and is mixed with a suitable filler, e.g. calcium carbonate, magnesium carbonate, silica or diatomaceous earth. Specifications 600,917 and 644,287 are referred to.
GB20044/48A 1947-12-26 1948-07-27 Improvements in electrostatic capacitors Expired GB679539A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US679539XA 1947-12-26 1947-12-26

Publications (1)

Publication Number Publication Date
GB679539A true GB679539A (en) 1952-09-17

Family

ID=22079507

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20044/48A Expired GB679539A (en) 1947-12-26 1948-07-27 Improvements in electrostatic capacitors

Country Status (1)

Country Link
GB (1) GB679539A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1108812B (en) * 1956-05-26 1961-06-15 Kondensatorenwerk Gera Veb Electrolyte for electrolytic capacitors
DE1121732B (en) * 1953-05-11 1962-01-11 Telefunken Patent Electrolytic capacitor
WO2002061777A1 (en) * 2001-02-01 2002-08-08 Epcos Ag Electrolyte for an aluminium-electrolyte capacitor, capacitor which uses the electrolyte and the use of said capacitor

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1121732B (en) * 1953-05-11 1962-01-11 Telefunken Patent Electrolytic capacitor
DE1108812B (en) * 1956-05-26 1961-06-15 Kondensatorenwerk Gera Veb Electrolyte for electrolytic capacitors
WO2002061777A1 (en) * 2001-02-01 2002-08-08 Epcos Ag Electrolyte for an aluminium-electrolyte capacitor, capacitor which uses the electrolyte and the use of said capacitor
US6876540B2 (en) 2001-02-01 2005-04-05 Epcos Ag Electrolyte for use in a capacitor

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