GB715231A - Improvements in or relating to alkyd resins - Google Patents
Improvements in or relating to alkyd resinsInfo
- Publication number
- GB715231A GB715231A GB11429/52A GB1142952A GB715231A GB 715231 A GB715231 A GB 715231A GB 11429/52 A GB11429/52 A GB 11429/52A GB 1142952 A GB1142952 A GB 1142952A GB 715231 A GB715231 A GB 715231A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- acetate
- ester
- alcohol
- amount
- 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
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/445—Block-or graft-polymers containing polysiloxane sequences containing polyester sequences
Abstract
An alkyd type resin is made by reacting (1) glycerine or pentaerythritol by heating with (2) a diester of terephthalic acid, isophthalic acid, a stilbene dicarboxylic acid, a diphenic acid, a tolane dicarboxylic acid or a dibenzyl dicarboxylic acid (the structure of the monocyclic aryl carboxylic acids being such that the carboxy groups are not ortho to each other) in which the alcoholic substituents of the ester are alkyl radicals, and (3) a silane or siloxane of the average general formula <FORM:0715231/IV (a)/1> where each R is an alkyl or monocyclic aryl, alkoxy or aryloxy radical, m has a value from 0 to 3, n has a value from 0.05 to 4, the sum of m+n being not greater than 4, and X is an alkoxy or aryloxy radical or a chlorine or bromine atom, the reactants (1) and (2) being employed in such an amount that the ratio of OH to the corresponding ester radical is from 4 : 1 to 1.001 : 1, and the reactant (3) is present in amount of 0.1 to 85 per cent. by weight of the total reactants. The organosilicon reactant is preferably incorporated in the alcohol-ester resin after removal of the theoretical amount of alcohol from transesterification of the acid-ester and the polyhydric alcohol. Reaction of the organosilicon component with the ester resin is effected preferably at 180 DEG to 260 DEG C. and the resulting products are cured at 200 DEG C. or above. The resins may be prepared in the presence of solvents such as quinoline, isoquinoline, tributylamine, triisobutylamine, triamylamine, isophorone, acetophenone, acetonyl acetone, dimethylformamide, diethylformamide, dimethyl acetamide, 2-ethylhexyl acetate, lauryl acetate, 2-ethylhexyl butyrate, butyl carbitolacetate, butyl cellosolve acetate, amylcarbitol acetate, diethylene glycol dipropionate, phenoxyethylene glycol acetate, diethylcarbitol, cresol and toluene; the solvent being present in amount sufficient to prevent gelation of the resin. The preferred aryl polycarboxylic acid diesters are formed from an alcohol from methanol to octanol. The resins, with or without conventional fillers, catalysts and mould lubricants are used as magnet wire enamels, for panel coating of automobiles, furnaces, stoves and smokestacks and for laminating and moulding purposes. In the example, phenylmethyldiethoxysilane was reacted with the product obtained by reacting glycerine and diethylterephthalate in the presence of zinc and calcium oxides. The product was fairly soluble in cyclohexanone. Specifications 583,754, 650,247 and 685,173 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US715231XA | 1951-05-31 | 1951-05-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB715231A true GB715231A (en) | 1954-09-08 |
Family
ID=22101868
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB11429/52A Expired GB715231A (en) | 1951-05-31 | 1952-05-06 | Improvements in or relating to alkyd resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB715231A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0075326A1 (en) * | 1981-09-23 | 1983-03-30 | Dow Corning Corporation | Non-precondensed silicone-alkyd resins and a method for their preparation |
-
1952
- 1952-05-06 GB GB11429/52A patent/GB715231A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0075326A1 (en) * | 1981-09-23 | 1983-03-30 | Dow Corning Corporation | Non-precondensed silicone-alkyd resins and a method for their preparation |
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