GB996649A - Improvements in or relating to ester imide resins - Google Patents
Improvements in or relating to ester imide resinsInfo
- Publication number
- GB996649A GB996649A GB38043/63A GB3804363A GB996649A GB 996649 A GB996649 A GB 996649A GB 38043/63 A GB38043/63 A GB 38043/63A GB 3804363 A GB3804363 A GB 3804363A GB 996649 A GB996649 A GB 996649A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ester
- glycerol
- coconut oil
- trimellitic anhydride
- 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
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
- H01B3/303—Macromolecular 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
- H01B3/306—Polyimides or polyesterimides
-
- 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
- C08G73/00—Macromolecular 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
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/16—Polyester-imides
-
- 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
Abstract
A method of making an ester-imide resin according to any of Claims 1 to 4 of the parent Specification, wherein the ester imide formed contains aliphatic residues derived from one or monocarboxylic acids having 6 to 24 carbon atoms, comprises introducing said residues by reacting the ester-imide resin or one of the starting materials for the preparation thereof with monocarboxylic acid or acids. Specified monocarboxylic acids are those derived from tallow, olive, soya bean, linseed and coconut oil and 2-ethylhexanoic acid. The examples describe the preparation of modified polyestermides from: (1) a mixed ester derived from dimethyl terephthalate, glycerol, butanediol and coconut oil and a diimide made from trimellitic anhydride and 4 : 41-diaminodiphenylmethane; (2) a condensate from glycerol, natural fatty acids, isophthalic acid and butanediol, 4 : 41-diaminodiphenyl methane and trimellitic anhydride, and (3) a diimide made from 4 : 41-diaminodiphenyl methane and trimellitic anhydride, coconut oil and glycerol. The products of the examples are soluble in benzene hydrocarbons, chlorinated hydrocarbons, ketones or esters and may be reacted with cross-linking agents for example amino - triazine - alcohol - formaldehyde condensates and stabilized polyisocyanates.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEB0069201 | 1962-10-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB996649A true GB996649A (en) | 1965-06-30 |
Family
ID=6976199
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB38043/63A Expired GB996649A (en) | 1962-10-12 | 1963-09-26 | Improvements in or relating to ester imide resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB996649A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4751107A (en) * | 1985-05-17 | 1988-06-14 | Basf Aktiengesellschaft | Heat-curable hot-melt enamel and its preparation |
-
1963
- 1963-09-26 GB GB38043/63A patent/GB996649A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4751107A (en) * | 1985-05-17 | 1988-06-14 | Basf Aktiengesellschaft | Heat-curable hot-melt enamel and its preparation |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2678934A (en) | Method of making glyceride-fumaric acid reaction products | |
GB1018032A (en) | Water soluble or dispersible surface coating ester resins | |
GB1007163A (en) | Process for the production of hardenable products by polyesterification | |
GB991020A (en) | Esterification of iso- and terephthalic acids | |
GB996649A (en) | Improvements in or relating to ester imide resins | |
GB1037405A (en) | A process for the preparation of modified polyethylene waxes | |
GB962974A (en) | Process for preparing oil-containing binders suitable for the preparation of water-based binder compositions | |
GB996745A (en) | Self-copolymerizable resinous compositions | |
GB630924A (en) | Alkyd resins | |
GB988828A (en) | Modified polyesters | |
GB1044179A (en) | A process for preparing water soluble alkyd resins | |
GB1272054A (en) | Unsaturated polyester resins, method of their production and application | |
GB961611A (en) | Improvements in and relating to alkyd resins | |
GB987191A (en) | Epoxy modified alkyd resins | |
GB1101380A (en) | Epoxy resin compositions | |
US2907735A (en) | Esterified epoxy polyesters | |
GB816413A (en) | Process for the production of highly porous and more especially hard light-weight materials | |
GB968223A (en) | Process for the preparation of alkyd resins | |
US2028914A (en) | Production of resin like materials | |
GB998356A (en) | Polymeric anhydrides | |
GB1023140A (en) | Polyester lacquers | |
GB963969A (en) | Process for producing oil-modified alkyd resins | |
GB1279257A (en) | Production of alkyd resins | |
SU124571A1 (en) | The method of obtaining varnish resins | |
GB745706A (en) | Improvements in or relating to silicone resins |