GB1074401A - Improvements in or relating to insulating material - Google Patents
Improvements in or relating to insulating materialInfo
- Publication number
- GB1074401A GB1074401A GB1657565A GB1657565A GB1074401A GB 1074401 A GB1074401 A GB 1074401A GB 1657565 A GB1657565 A GB 1657565A GB 1657565 A GB1657565 A GB 1657565A GB 1074401 A GB1074401 A GB 1074401A
- Authority
- GB
- United Kingdom
- Prior art keywords
- peroxide
- reaction product
- butyl
- benzoyl peroxide
- bisphenol
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
- C08L63/10—Epoxy resins modified by unsaturated compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/20—Esters of polyhydric alcohols or polyhydric phenols, e.g. 2-hydroxyethyl (meth)acrylate or glycerol mono-(meth)acrylate
Abstract
Non-electrically conductive fibres, e.g. glass fibres, suitable for forming electrical insulation material are bound together with a resinous material including a copolymer obtained by polymerizing the reaction product of 2 molar proportions of methacrylic acid and 1 molar proportion of the diglycidyl ether of bisphenol-A, which is substantially free from unreacted epoxy groups, with an ethylenically unsaturated comonomer in the presence of benzoyl peroxide and one or more peroxy catalysts which promote a polymerization rate, with respect to said reaction product and comonomer, greater than that achieved with benzoyl peroxide. Suitable comonomers include styrene, diallyl phthalate, triallyl cyanurate, unsaturated polyesters, acetyl triallyl citrate, vinyl toluene, divinylbenzene, polymerizable phosphorus compounds (unspecified), and dialkyl maleates and fumarates. Peroxy compounds suitable as catalyst components include t-butyl perbenzoate, t-butyl hydroperoxide, dicumyl peroxide, cyclohexanone peroxide, cyclohexyl hydroperoxide, 2,4-dichlorobenzoyl peroxide, methyl amyl ketone peroxide, lauroyl peroxide, methylcyclohexyl hydroperoxide, di-t-butyl dipermaleate and di-t-butyl diperphthalate. Inert fillers, e.g. calcium carbonate or mica, mould release agents, e.g. zinc, calcium and aluminium stearates, and colouring materials may be included in the resinous binder. In an example, the bisphenol-A derivative reaction product and styrene are copolymerized in bulk in the presence of filler, pigment and mould release agent.ALSO:Non-electrically conductive fibres, e.g. glass fibres, are bound together to form an electrical insulator with a resinous material including a copolymer obtained by polymerising the reaction product of 2 molar proportions of methacrylic acid and 1 molar proportion of the diglycidyl ether of bisphenol-A (the reaction product being substantially free from unreacted epoxy groups) with an ethylenically unsaturated comonomer in the presence of benzoyl peroxide and at least one peroxy catalyst which promotes a polymerisation rate greater than that achieved with benzoyl peroxide. Suitable comonomers include styrene diallyl phthalate, triallyl cyanurate, unsaturated polyesters, acetyl triallyl citrate, vinyl toluene, compounds (unspecified), and dialkyl maleates and fumarates. The resinous material may include an inert filler, e.g. calcium carbonate or mica, a mould release agent, e.g. zinc, calcium or aluminium stearate, and a colouring material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1657565A GB1074401A (en) | 1965-04-20 | 1965-04-20 | Improvements in or relating to insulating material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1657565A GB1074401A (en) | 1965-04-20 | 1965-04-20 | Improvements in or relating to insulating material |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1074401A true GB1074401A (en) | 1967-07-05 |
Family
ID=10079781
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1657565A Expired GB1074401A (en) | 1965-04-20 | 1965-04-20 | Improvements in or relating to insulating material |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1074401A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0018638A1 (en) * | 1979-05-01 | 1980-11-12 | Union Carbide Corporation | A poly(acrylate) containing composition and process for producing molded articles |
EP0063913A2 (en) * | 1981-04-21 | 1982-11-03 | Sumitomo Electric Industries Limited | Heat-shrinkable tubes |
-
1965
- 1965-04-20 GB GB1657565A patent/GB1074401A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0018638A1 (en) * | 1979-05-01 | 1980-11-12 | Union Carbide Corporation | A poly(acrylate) containing composition and process for producing molded articles |
EP0063913A2 (en) * | 1981-04-21 | 1982-11-03 | Sumitomo Electric Industries Limited | Heat-shrinkable tubes |
EP0063913A3 (en) * | 1981-04-21 | 1984-01-11 | Sumitomo Electric Industries Limited | Heat-shrinkable tubes |
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