GB676372A - Improvements in or relating to copolyesters and their use for electrical insulation - Google Patents
Improvements in or relating to copolyesters and their use for electrical insulationInfo
- Publication number
- GB676372A GB676372A GB18711/49A GB1871149A GB676372A GB 676372 A GB676372 A GB 676372A GB 18711/49 A GB18711/49 A GB 18711/49A GB 1871149 A GB1871149 A GB 1871149A GB 676372 A GB676372 A GB 676372A
- Authority
- GB
- United Kingdom
- Prior art keywords
- copolyester
- solvent
- acid
- copolyesters
- heated
- 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
Links
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
- H01B3/30—Insulators 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
- H01B3/42—Insulators 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 polyesters; polyethers; polyacetals
- H01B3/421—Polyesters
- H01B3/422—Linear saturated polyesters derived from dicarboxylic acids and dihydroxy compounds
- H01B3/423—Linear aromatic polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
- C08G63/181—Acids containing aromatic rings
- C08G63/183—Terephthalic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
-
- 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
- H01B3/30—Insulators 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
- H01B3/307—Other macromolecular compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Insulating Materials (AREA)
Abstract
The Specification claims a copolyester of ethylene glycol, terephthalic acid and an acid of formula CnH2n(COOH)2, where n is 2-8, the copolyester having 2-4 molecular proportions of combined terephthalic acid for every molecular proportion of combined aliphatic dibasic acid. Reaction between the three ingredients is preferably continued till the copolyester has a molecular weight of 10,000 or more or alternatively a lower molecular weight copolyester may be treated with a polyisocyanate whereby the molecular weight is 10,000 or more. The copolyesters may be used as insulating coverings for conductors (see Group XXXVI) in which case they may be applied to the conductor (a) dissolved in a solvent, e.g. o-cresol, cresylic acid, xylenols, a solution of phenol in a cresol, or a mixture of phenols and tetrachloroethane or monochlorobenzene; (b) in the form of a dispersion in a non-solvent, e.g. a petroleum hydrocarbon; (c) in a latent-solvent which develops solvent properties only at elevated temperatures; or (d) from a melt, e.g. by extrusion of the melted copolyester, if desired together with a solvent. The copolyesters form compositions with polyamides, alkyds, phenol formaldehyde condensates, urea- and melamine-formaldehyde condensates which may be alkylated, polyvinyl acetals, shellac, wood flour, paper, asbestos, mica, glass and fire retardants, e.g. halo-hydrocarbons. The copolyesters may be modified by heating with lightly condensed phenol-formaldehyde condensates, dimethylol urea, hexamethylol melamine, dimethylol urea dibutyl ether, or hexamethylol melamine hexamethyl ether, if desired in presence of maleic acid, phthalic anhydride, ammonium hydrogen phosphate, styrene dichloride, a bromonaphthol or 2 : 4-dichloro-1-naphthol. The copolyester insulation may be applied directly to the surface of the conductor or over another insulating covering, e.g. polyvinyl acetal. In examples: (1) dimethyl terephthalate and ethylene glycol are heated in presence of litharge and the product heated with adipic acid. The copolyester by itself and in combination with hexamethylol melamine hexamethyl ether is dissolved in cresol and used for insulating copper; (2), (3) and (4) dimethyl terephthalate and ethylene glycol are heated in presence of litharge and the products heated respectively with sebacic, glutaric and succinic acids. The invention of Specification 650,358 is disclaimed.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE497002D BE497002A (en) | 1949-07-15 | ||
GB18711/49A GB676372A (en) | 1949-07-15 | 1949-07-15 | Improvements in or relating to copolyesters and their use for electrical insulation |
US17323850 US2683100A (en) | 1949-07-15 | 1950-07-11 | Copolyesters and their use for electrical insulation |
FR1023860D FR1023860A (en) | 1949-07-15 | 1950-07-13 | Improvements relating to copolyesters and their application to electrical insulation |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1023860X | 1949-07-15 | ||
GB18711/49A GB676372A (en) | 1949-07-15 | 1949-07-15 | Improvements in or relating to copolyesters and their use for electrical insulation |
Publications (1)
Publication Number | Publication Date |
---|---|
GB676372A true GB676372A (en) | 1952-07-23 |
Family
ID=26253560
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB18711/49A Expired GB676372A (en) | 1949-07-15 | 1949-07-15 | Improvements in or relating to copolyesters and their use for electrical insulation |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB676372A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3442868A (en) * | 1965-07-20 | 1969-05-06 | Teijin Ltd | Novel process for the preparation of polyester |
US3497473A (en) * | 1966-11-29 | 1970-02-24 | American Enka Corp | Process for the preparation of polyethylene terephthalate |
DE1807776A1 (en) * | 1968-11-08 | 1970-05-27 | Dynamit Nobel Ag | Production of boil-proof, sterilizable and highly deformable lacquer films |
DE19754327A1 (en) * | 1997-12-08 | 1999-06-10 | Herberts Gmbh | Powder coating compositions suitable for weather-resistant coatings |
EP1343052A2 (en) * | 2002-03-05 | 2003-09-10 | Fujitsu Limited | A resist pattern-improving material and a method for preparing a resist pattern by using the same |
-
1949
- 1949-07-15 GB GB18711/49A patent/GB676372A/en not_active Expired
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3442868A (en) * | 1965-07-20 | 1969-05-06 | Teijin Ltd | Novel process for the preparation of polyester |
US3497473A (en) * | 1966-11-29 | 1970-02-24 | American Enka Corp | Process for the preparation of polyethylene terephthalate |
DE1807776A1 (en) * | 1968-11-08 | 1970-05-27 | Dynamit Nobel Ag | Production of boil-proof, sterilizable and highly deformable lacquer films |
DE19754327A1 (en) * | 1997-12-08 | 1999-06-10 | Herberts Gmbh | Powder coating compositions suitable for weather-resistant coatings |
EP1343052A2 (en) * | 2002-03-05 | 2003-09-10 | Fujitsu Limited | A resist pattern-improving material and a method for preparing a resist pattern by using the same |
EP1343052A3 (en) * | 2002-03-05 | 2003-11-19 | Fujitsu Limited | A resist pattern-improving material and a method for preparing a resist pattern by using the same |
US7416837B2 (en) | 2002-03-05 | 2008-08-26 | Fujitsu Limited | Resist pattern-improving material and a method for preparing a resist pattern by using the same |
CN1442752B (en) * | 2002-03-05 | 2012-10-03 | 富士通株式会社 | Anticorrosion image improved material |
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