GB729883A - Improvements in or relating to copolymerizable compositions - Google Patents

Improvements in or relating to copolymerizable compositions

Info

Publication number
GB729883A
GB729883A GB23547/53A GB2354753A GB729883A GB 729883 A GB729883 A GB 729883A GB 23547/53 A GB23547/53 A GB 23547/53A GB 2354753 A GB2354753 A GB 2354753A GB 729883 A GB729883 A GB 729883A
Authority
GB
United Kingdom
Prior art keywords
maleic
polycarboxylic acids
aconitic
fumaric
styrene
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
GB23547/53A
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.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid Co
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 American Cyanamid Co filed Critical American Cyanamid Co
Publication of GB729883A publication Critical patent/GB729883A/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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/52Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
    • C08G63/56Polyesters derived from ester-forming derivatives of polycarboxylic acids or of polyhydroxy compounds other than from esters thereof
    • C08G63/58Cyclic ethers; Cyclic carbonates; Cyclic sulfites ; Cyclic orthoesters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A copolymerizable composition comprises (1) a polyglycidyl ester of a polycarboxylic acid, (2) an a ,b -unsaturated polycarboxylic acid or anhydride and (3) styrene or a derivative. In a modification ingredients (1) and (2) may be partially polymerized. The esters may be derived from phthalic, oxalic, malonic, succinic, glutaric, sebacic, adipic, pimelic, suberic, azelaic, tricarballylic, citric, tartaric, malic, maleic, fumaric, aconitic and itaconic acids (see Group IV (b)), and ingredient (2) may be maleic, fumaric, aconitic or itaconic acid. Styrenes specified are styrene, a -methyl-, a -ethyl-, a -chloro-, o-methyl-, m-propyl-, p-ethyl-, o-, m- and p-chloro-, 2,4-dimethyl-, 2,5-dimethyl-, 3,4-diethyl-, 2,5-dichloro- and 3,5-dichlorostyrenes and mixtures. The polymerization may be carried out with heating alone (example 1) but is preferably effected in the presence of a catalyst such as t.-butyl hydroperoxide or di-t.-butyl- or methyl ethyl ketone-peroxide. In examples the curing is carried out in two stages and examples 2 and 3 include as a further ingredient a polyester derived from maleic and phthalic anhydrides, propylene glycol and pentaerythritol. The products are tough and of low shrinkage.ALSO:Polyglycidyl esters of polycarboxylic acids are prepared by reaction of reactive halohydrins, such as epichlorohydrin, epibromohydrin, epiiodohydrin and epifluorohydrin, with alkali or alkaline-earth salts of the polycarboxylic acids. In particular dipotassium phthalate and epichlorohydrin are reacted at 105-110 DEG C. with a quaternary ammonium salt as catalyst. The potassium chloride produced and excess epichlorohydrin are removed to give diglycidyl phthalate which is purified by vacuum distillation. Other polycarboxylic acids specified are oxalic, malonic, succinic, glutaric, sebacic, adipic, pimelic, suberic, azelaic, tricarballylic, citric, tartaric, malic, maleic, fumaric, aconitic and itaconic. The polyglycidyl esters may be polymerized with a ,b -unsaturated polycarboxylic acids and styrene or its derivatives (see Group IV (a)).
GB23547/53A 1952-09-10 1953-08-26 Improvements in or relating to copolymerizable compositions Expired GB729883A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US729883XA 1952-09-10 1952-09-10

Publications (1)

Publication Number Publication Date
GB729883A true GB729883A (en) 1955-05-11

Family

ID=22111014

Family Applications (1)

Application Number Title Priority Date Filing Date
GB23547/53A Expired GB729883A (en) 1952-09-10 1953-08-26 Improvements in or relating to copolymerizable compositions

Country Status (1)

Country Link
GB (1) GB729883A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4304695A (en) 1979-08-29 1981-12-08 Bayer Aktiengesellschaft Air-drying, fatty acid-modified lacquer binders, based on fumaric or maleic acid bis-glycidyl ester copolymers

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4304695A (en) 1979-08-29 1981-12-08 Bayer Aktiengesellschaft Air-drying, fatty acid-modified lacquer binders, based on fumaric or maleic acid bis-glycidyl ester copolymers

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