GB760006A - Improvements in or relating to synthetic ether-resin copolymers - Google Patents

Improvements in or relating to synthetic ether-resin copolymers

Info

Publication number
GB760006A
GB760006A GB3393/53A GB339353A GB760006A GB 760006 A GB760006 A GB 760006A GB 3393/53 A GB3393/53 A GB 3393/53A GB 339353 A GB339353 A GB 339353A GB 760006 A GB760006 A GB 760006A
Authority
GB
United Kingdom
Prior art keywords
acids
fatty acids
styrene
vinyl toluene
ether
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
GB3393/53A
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.)
Lewis Berger and Sons Ltd
Original Assignee
Lewis Berger and Sons 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 Lewis Berger and Sons Ltd filed Critical Lewis Berger and Sons Ltd
Publication of GB760006A publication Critical patent/GB760006A/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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/14Polycondensates modified by chemical after-treatment
    • C08G59/1433Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
    • C08G59/1438Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing oxygen
    • C08G59/1455Monocarboxylic acids, anhydrides, halides, or low-molecular-weight esters thereof
    • C08G59/1461Unsaturated monoacids
    • C08G59/1472Fatty acids

Abstract

Esters with drying properties are formed by esterifying an ether resin with an unsaturated acid which has been copolymerized with a vinyl monomer before or during the esterification. Ether resins are formed from polyhydric compounds many of which are listed in the Specification, and epi- or di-halohydrins, or polyepoxides, e.g. bis-(2,3-epoxypropyl)ether or butylene di-oxide. Monofunctional chain-terminating agents may be included in the reaction mixture if desired. Many vinyl monomers and many unsaturated acids are mentioned in the Specification. They may be copolymerized with the aid of benzoyl peroxide, di-tert.-butyl peroxide, sulphur, sulphur dioxide or a redox catalyst, e.g. a mixture of dodecyl mercaptan and benzoyl peroxide. Other catalysts are also mentioned. Solvents may be employed, e.g. xylol. Examples describe the production of copolymers as follows: B-1, B-8 and B-9, linseed oil fatty acids-styrene; B-2, dehydrated castor oil fatty acids-styrene; B-3, dehydrated castor oil fatty acids-acrylonitrile; B-4 to B-7, soybean fatty acids-styrene; B-10, B-11, linseed oil acids-vinyl toluene; B-12 to B-14, soya bean fatty acids-vinyl toluene; B-15 to B-17, Isoline fatty acids (from dehydrated castor oil)-styrene; B-18, Isoline acids-vinyl toluene; B-19 tung oil acids-vinyl toluene; B-20, soya bean acids-isobutylene; B-21, soya bean acids-p-methoxy styrene. A number of examples then describe the esterification of these copolymers with ether resins produced from epichlorhydrin and di-(4-hydroxyphenyl) dimethyl methane. In some examples benzoic acid was also included in the reaction mixture. The products are soluble in xylol and are film-forming.
GB3393/53A 1952-02-08 1953-02-06 Improvements in or relating to synthetic ether-resin copolymers Expired GB760006A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US760006XA 1952-02-08 1952-02-08

Publications (1)

Publication Number Publication Date
GB760006A true GB760006A (en) 1956-10-31

Family

ID=22129289

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3393/53A Expired GB760006A (en) 1952-02-08 1953-02-06 Improvements in or relating to synthetic ether-resin copolymers

Country Status (1)

Country Link
GB (1) GB760006A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3014882A (en) * 1956-09-14 1961-12-26 Shell Oil Co Vinyl chloride polymer compositions having improved impact strength

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3014882A (en) * 1956-09-14 1961-12-26 Shell Oil Co Vinyl chloride polymer compositions having improved impact strength

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