GB804537A - Process for the preparation of unsaturated polyester resin mixtures - Google Patents
Process for the preparation of unsaturated polyester resin mixturesInfo
- Publication number
- GB804537A GB804537A GB13907/57A GB1390757A GB804537A GB 804537 A GB804537 A GB 804537A GB 13907/57 A GB13907/57 A GB 13907/57A GB 1390757 A GB1390757 A GB 1390757A GB 804537 A GB804537 A GB 804537A
- Authority
- GB
- United Kingdom
- Prior art keywords
- unsaturated
- epoxidized
- oil
- acid
- glycols
- 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
- 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
- C08G63/52—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
- C08G63/54—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation the acids or hydroxy compounds containing carbocyclic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Abstract
Unsaturated polyester mixtures which can be polymerized in presence of air to give nontacky films suitable for use as lacquers or casting resins are obtained by incorporating a partially epoxidized unsaturated oil into a polyester formed from one or more unsaturated dicarboxylic acids and one or more polyglycols and combining the resulting modified unsaturated polyester with a monomeric polymerizable vinyl compound. Unsaturated polyesters are obtained in known manner by esterification with glycols of a ,b -unsaturated dicarboxylic acids, e.g. fumaric, maleic acids or their anhydrides. Glycols specified are ethylene, diethylene triethylene glycols, 1,2-, 1,3-propane diols and 1,3-, 1,4-butane diols. Unsaturated oils which may be epoxidized are soya, linseed, hemp seed, castor, perilla and wood oils and synthetic oils, e.g. tall oils, fatty acid esterified with polyhydric alcohols. The partially epoxidized oil should have an iodine number of 100-150 after epoxidization. An inhibitor, e.g. hydroquinone, tertiary butyl pyrocatechol may be dissolved in the vinyl compound, e.g. styrene, to prevent premature copolymerization. Organic hydroperoxides or peroxides may be used as catalysts together with accelerators, e.g. cobalt naphthenate or dimethyl aniline. Saturated mono or dicarboxylic acids and monohydric alcohols may be used in addition to the unsaturated acids and glycols. The epoxidized oil may be added when the unsaturated polyester ingredients have been reacted to the required acid number. In examples: (1) linseed oil of acid No. 180 is epoxidized by reaction with hydrogen peroxide and formic acid to give a product having an epoxy content of 2.6 per cent. Maleic anhydride, phthalic anhydride and 1,2-propane diol are melted and heated to 180-250 DEG C. under carbon dioxide until a product having an acid No. of 120 is obtained and the product is then reacted with the epoxidized linseed oil. The product is cooled and mixed with styrene and hydroquinone and then with a 10 per cent solution of cobalt naphthenate in styrene. The mixture shortly before use is mixed with a 40 per cent methyl ethyl ketonehydroperoxide solution or a 50 per cent cyclohexanone-hydroperoxide solution in dimethyl phthalate and sprayed on to a surface. In examples: (2) p-tert.-butyl benzoic acid, (3) a hydrogenated resin acid, (4) an unsaturated C16-C18 fatty alcohol are used as constituents of the polyester reactants. In Example (5) the epoxidized oil is obtained from fish oil.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE804537X | 1956-05-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB804537A true GB804537A (en) | 1958-11-19 |
Family
ID=6722125
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB13907/57A Expired GB804537A (en) | 1956-05-02 | 1957-05-01 | Process for the preparation of unsaturated polyester resin mixtures |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB804537A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3291765A (en) * | 1962-03-19 | 1966-12-13 | Allied Chem | Process for producing oil-modified alkyd resins and such resins |
-
1957
- 1957-05-01 GB GB13907/57A patent/GB804537A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3291765A (en) * | 1962-03-19 | 1966-12-13 | Allied Chem | Process for producing oil-modified alkyd resins and such resins |
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