GB715231A - Improvements in or relating to alkyd resins - Google Patents

Improvements in or relating to alkyd resins

Info

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
Application number
GB11429/52A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dow Silicones UK Ltd
Original Assignee
Dow Corning Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Dow Corning Ltd filed Critical Dow Corning Ltd
Publication of GB715231A publication Critical patent/GB715231A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/42Block-or graft-polymers containing polysiloxane sequences
    • C08G77/445Block-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.
GB11429/52A 1951-05-31 1952-05-06 Improvements in or relating to alkyd resins Expired GB715231A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (1)

* Cited by examiner, † Cited by third party
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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