GB758724A - Improvements relating to synthetic resins - Google Patents
Improvements relating to synthetic resinsInfo
- Publication number
- GB758724A GB758724A GB24009/53A GB2400953A GB758724A GB 758724 A GB758724 A GB 758724A GB 24009/53 A GB24009/53 A GB 24009/53A GB 2400953 A GB2400953 A GB 2400953A GB 758724 A GB758724 A GB 758724A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acids
- alcohol
- peroxide
- copolymer
- reacting
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
A synthetic resin for use in paints, varnishes and baking enamels is the reaction product of a copolymer of an unsaturated monocarboxylic fatty acid and a monovinyl aromatic compound, a polyhydric alcohol and a polysiloxane containing alkoxy groups, and/or halogen atoms. The resin may be made by reacting the siloxane with the alcohol and with the copolymer, but is preferably made by reacting the alcohol with the copolymer and reacting the resulting ester with the siloxane. There are specified (a) monovinyl aromatic compounds-styrene, a - methylstyrene, p-methylstyrene, a -p-dimethylstyrene, divinylbenzene, vinylnaphthalene, acenaphthylene, vinyltoluene, p-chlorostyrene, p-trichloromethylstyrene, 2 : 5-dichlorostyrene, p-methoxystyrene or mixtures thereof; (b) unsaturated fatty acids-acrylic, methacrylic, vinylacetic, hydrosorbic, decenoic, undecylenic, sorbic, hiragonic, linoleic, isolinoleic, elaeostearic, punicic, parinaric, arachidonic, clupanodonic, scoliodonic, nisinic, tariric, abietic and licanic acids; castor-, linseed-, soyabean-and tung-oil fatty acids, rosin acids and tall oil acids; the dimers and trimers of these acids may also be used; (c) polyhydric alcohols-ethylene-, diethylene-, propylene- and trimethylene-glycols, glycerine, trimethylol propane, pentaerythritol, polyallyl alcohol, sorbito-and mannitol. The alkoxy polysiloxanes specified conform to the formula <FORM:0758724/IV(a)/1> where R is a lower alkyl radical (i.e. of 1 to 4 C atoms), R1 is an alkyl or aryl radical, R11 is R1 or alkoxy and n is at least 2. The halogenopolysiloxanes specified are dimethyltriphenyltrichlorotrisiloxane and trimethyltriphenyldichlorotrisiloxane. In making the copolymers, the proportions by weight are preferably 5 to 75 per cent of the vinyl monomer and 95 to 25 per cent of the acid, and the reaction is desirably effected under reflux at 150 DEG to 475 DEG F. in the presence of a solvent and a catalyst or controlling agent, e.g. hydrogen peroxide, benzoyl peroxide, t-butyl peroxide, di-tertiary butyl peroxide, acetyl peroxide in dimethyl phthalate, fuller's earth, sulphur, sulphur dioxide, stannic chloride, boron trifluoride or a redox catalyst such as a mixture of dodecyl mercaptan and benzoyl peroxide or benzidine and sulphur dioxide, and desirably in an inert atmosphere, e.g. nitrogen or carbon dioxide. Examples A1 to A19 describe the preparation of the copolymers and examples B1 to B13 describe the preparation of the resinous reaction products. U.S.A. Specifications 2,415,389, 2,584,343 and 2,587,295 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US758724XA | 1952-09-09 | 1952-09-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB758724A true GB758724A (en) | 1956-10-10 |
Family
ID=22128501
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB24009/53A Expired GB758724A (en) | 1952-09-09 | 1953-08-31 | Improvements relating to synthetic resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB758724A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8258188B2 (en) | 2004-01-20 | 2012-09-04 | Josep Bassaganya-Riera | Method of using punicic acid to enhance immune response and prevent metabolic disorders |
-
1953
- 1953-08-31 GB GB24009/53A patent/GB758724A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8258188B2 (en) | 2004-01-20 | 2012-09-04 | Josep Bassaganya-Riera | Method of using punicic acid to enhance immune response and prevent metabolic disorders |
US8822543B2 (en) | 2004-01-20 | 2014-09-02 | Nutrition Therapeutics, Inc. | Method of using punicic acid to enhance immune response and prevent metabolic disorders |
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