GB1057727A - Improvements in or relating to electrically insulating varnishes and to electrically insulating materials produced therefrom - Google Patents

Improvements in or relating to electrically insulating varnishes and to electrically insulating materials produced therefrom

Info

Publication number
GB1057727A
GB1057727A GB4557863A GB4557863A GB1057727A GB 1057727 A GB1057727 A GB 1057727A GB 4557863 A GB4557863 A GB 4557863A GB 4557863 A GB4557863 A GB 4557863A GB 1057727 A GB1057727 A GB 1057727A
Authority
GB
United Kingdom
Prior art keywords
tetracarboxylic
tetracarboxylic acid
electrically insulating
ether
bis
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
GB4557863A
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.)
Beck & Co Dr GmbH
Original Assignee
Beck & Co Dr GmbH
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
Priority claimed from DEB69849A external-priority patent/DE1261672B/en
Application filed by Beck & Co Dr GmbH filed Critical Beck & Co Dr GmbH
Publication of GB1057727A publication Critical patent/GB1057727A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1003Preparatory processes
    • 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
    • H01B3/30Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/303Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups H01B3/38 or H01B3/302
    • H01B3/306Polyimides or polyesterimides

Abstract

A process for the preparation of an electrically insulating varnish comprises reacting (a) at least one tetracarboxylic acid dianhydride and/or at least one tetracarboxylic acid monoester monoanhydride in which the carboxyl group and the ester group are attached to adjacent carbon atoms, and/or at least one tetracarboxylic acid diester in which a carboxyl group and an ester group are attached to adjacent carbon atoms, with (b) at least one diprimary diamine containing at least 2 carbon atoms, at a temperature below 100 DEG C. in the presence of a solvent consisting of or including at least one phenol and at least 75 mol. per cent (based on the total amount of tetracarboxylic acid derivatives) of at least one volatile tertiary amine. The products may be converted by thermal or chemical treatment to polyimides. Specified diamines are benzidine, 4:41 - diaminophenylmethane, 4:41 - diaminophenylpropane, 4:41 - diaminophenylether, 4:41 - diaminophenylsulphone, 2:11 - diaminododecane, 4:41 - diaminophenyl sulphide, 1:2 - bis - (3 - aminopropoxy) ethane, 2:17 - diaminoeicosadecane, 1:4 - diaminocyclohexane, 1:10 - diamino - 1:10 - dimethyldecane, 1:12 - diamino octadecane, the bis-p-amino ethers of 4:41-dihydroxyldiphenyl, diphenylol propane, diphenylol methane, diphenylol ether, diphenylol sulphone and hydroquinone and m- and p-phenylene, 2:4 - toluylone, hexamethylene, octamethylene, nonamethylene, decamethylene, tetramethylene, 3 - methylheptamethylene, 4:4 - dimethylheptamethylene, - 2:2 - dimethylpropylene, 3 - methoxyhexamethylene, 2:5 - dimethylhexamethylene, 2:5 - dimethyl heptamethylene, 3 - methyl heptamethylene and 5 - methylnonamethylene diamine. Specified acid derivatives are those of pyromellitic, 2:3:6:7 - naphthalene tetracarboxylic, 3:31:4:41 - diphenyl tetracarboxylic, 1:2:5:6 - naphthalene tetracarboxylic, 2:21:3:31 - diphenyl tetracarboxylic, perylene - 3:4:9:10 - tetracarboxylic and ethylene tetracarboxylic acid, and bis - (3:4 - dicarboxyyphenyl) sulphone and bis - (3:4 - dicarboxyphenyl) ether. Specified solvents are phenol, cresol, xylenol and mixtures thereof, optionally admixed with benzene hydrocarbons or esters. Specified amines are N:N-dimethyl aniline, N:N-diethylaniline, pyridine, prioline, lutidine, collidine and quinoline.ALSO:A process for producing an electrically insulating coating comprises depositing a layer of a varnish made by reacting a tetracarboxylic acid dianhydride and/or a tetracarbocylic acid monoester monoanhydride and/or a tetracarboxylic acid diester with a primary diamine in the presence of a phenol and a volatile tertiary amine (see Division C3) on a base, removing the solvent therefrom and converting the residual product to a polyimide by thermal or chemical treatment. Examples 1 to 5 describe the coating of copper wire with polyimides derived from pyromellitic dianhydride and:- (1) and (4) 4:4\sv-diaminodiphenyl ether; (2) and (3) m-phenylene diamine and 4:4\sv-diaminophenyl ether, and (5) 4:4\sv-diphenylolpropone- 2:2- di (-p-aminophenyl) ether.
GB4557863A 1962-12-04 1963-11-19 Improvements in or relating to electrically insulating varnishes and to electrically insulating materials produced therefrom Expired GB1057727A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB69849A DE1261672B (en) 1962-12-04 1962-12-04 Process for the production of polycondensation products

Publications (1)

Publication Number Publication Date
GB1057727A true GB1057727A (en) 1967-02-08

Family

ID=6976441

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4557863A Expired GB1057727A (en) 1962-12-04 1963-11-19 Improvements in or relating to electrically insulating varnishes and to electrically insulating materials produced therefrom

Country Status (1)

Country Link
GB (1) GB1057727A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6133337A (en) * 1996-01-04 2000-10-17 Basf Aktiengesellschaft Use of reactive prepolymeric organic compounds

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6133337A (en) * 1996-01-04 2000-10-17 Basf Aktiengesellschaft Use of reactive prepolymeric organic compounds

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