GB923095A - Improvements in and relating to synthetic resins - Google Patents

Improvements in and relating to synthetic resins

Info

Publication number
GB923095A
GB923095A GB2920961A GB2920961A GB923095A GB 923095 A GB923095 A GB 923095A GB 2920961 A GB2920961 A GB 2920961A GB 2920961 A GB2920961 A GB 2920961A GB 923095 A GB923095 A GB 923095A
Authority
GB
United Kingdom
Prior art keywords
methyl
vinyl
ethyl
groups
dimethyl
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
GB2920961A
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.)
Union Carbide Corp
Original Assignee
Union Carbide Corp
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 Union Carbide Corp filed Critical Union Carbide Corp
Publication of GB923095A publication Critical patent/GB923095A/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
    • C08G59/02Polycondensates containing more than one epoxy group per molecule
    • C08G59/027Polycondensates containing more than one epoxy group per molecule obtained by epoxidation of unsaturated precursor, e.g. polymer or monomer
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F279/00Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
    • C08F279/02Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Paints Or Removers (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

A curable composition comprises an epoxidized polymer of a conjugated diene and containing at least 1% oxirane oxygen, a polycarboxylic acid compound, and a monomeric ethylenically unsaturated compound which contains no functional groups which are reactive with vicinal epoxy groups, hydroxy groups and carboxy groups, at least one component other than the monomer possessing at least one ethylenic group, the components being in such relative amounts as to provide from 0,1 to 2,5 carboxy groups of the acid compound per epoxy group and from 0,002 to 3,0 ethylenic groups of the monomeric ethylenically unsaturated compound per ethylenic group of the other components. The composition may contain a polyol in amount to provide up to 2,0 hydroxyl groups of polyol per epoxy group of the epoxidized polymer. Specified dienes are butadiene, 1- and 2-methyl-butadiene, 2-ethyl-, 1-1-dimethyl, 1-4-dimethyl, 2-3-dimethyl, 2-isopropyl, 1-n-propyl, 1-phenyl, 1-ethoxy, 1-acetoxy, 1-allyl, butadienes and 2-methyl-6-methylene-2-7-octadiene. These dienes may be copolymerized with ethylene, higher olefins, styrene, vinyl toluene, isopropenyl benzene, 4-vinyl-cyclohexene, divinyl benzene, vinyl chloride bromide and fluoride, allyl chloride, alpha-methyl-styrene, alphachlorostyrene, 2-5-dichlorostyrene, 4-cyanostyrene, 2-hydroxystyrene, 2-acetoxystyrene, chlorotrifluoroethylene, vinylidene chloride and fluoride, methyl acrylate, methyl, ethyl and octyl methacrylate, methyl, ethyl and butyl crotonate, dimethyl, dibutyl and dioctyl maleate, diethyl fumarate and chloromaleate, vinyl acetate, butyrate, stearate, oleate, linoleate, benzoate and crotonate, vinyl 2-ethylhexanoate, allyl acetate, acrylonitrile and methacrylonitrile, acrylamide, methacrylamide, crotonamide, N-vinyl benzamide, N-vinyl-butyramide, methyl vinyl ketone, methyl isopropenyl ketone, acrolein, vinyl ethyl ether, vinyl butyl ether, 2-vinylpyridine and N-vinylcarbazole. Specified polycarboxylic acid compounds include phthalic, tetrahydrophthalic hexahydrophthalic, chlorendic, maleic, chloromaleic, dichloromaleic, citraconic, isocitraconic, glutaric, adipic, succinic, itaconic, heptylsuccinic, 4-nitrophthalic, the naphthalic, tetraallylphthalic, lower allyl substituted bicyclo[2,21]hept-5-ene-2-3-dicarboxylic and methyl bicyclo[2,2,1]-hept-5-ene-2-3-dicarboxylic anhydrides. Maleic anhydride is preferred. A long list of monomeric ethylenic compounds is given including most of those listed above and also containing dienes and cycloalkenes. Many polyols are listed-1-2-6-hexanediol and triol, glycerol, ethylene glycol, 1-1-1-trimethylolpropane, resorcinol, diethylene glycol and 1-4-butanediol being used in examples. Acid or basic catalysts, e.g. boron fluoride, aluminium chloride, and other metal halide Lewis acids, stray mineral acids, the aliphatic and aromatic hydrocarbon sulphonic acids, the alkali metal hydroxides, and amines may be present, particularly when dissolved in solvents such as the organic ethers, esters and ketones. Free radical catalysts, e.g. peroxides, hydroperoxides and peresters may be present as may also activators, e.g. cobalt naphthenate and octanoate and lead octanoate. The compositions may be cured either partially and/or completely especially in a liquid vehicle, e.g. toluene, xylene, benzene, methyl ethyl ketone, and butyl, ethyl and amyl acetates. Specification 860,354 is referred to.
GB2920961A 1960-08-24 1961-08-14 Improvements in and relating to synthetic resins Expired GB923095A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US5153160A 1960-08-24 1960-08-24
US5153360A 1960-08-24 1960-08-24

Publications (1)

Publication Number Publication Date
GB923095A true GB923095A (en) 1963-04-10

Family

ID=26191992

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2920961A Expired GB923095A (en) 1960-08-24 1961-08-14 Improvements in and relating to synthetic resins

Country Status (2)

Country Link
FR (1) FR1315735A (en)
GB (1) GB923095A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0171626A2 (en) * 1984-07-16 1986-02-19 Nippon Petrochemicals Company, Limited Adhesive resins and laminate articles
US4737548A (en) * 1984-07-16 1988-04-12 Nippon Petrochemicals Adhesive resins and laminate articles

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0171626A2 (en) * 1984-07-16 1986-02-19 Nippon Petrochemicals Company, Limited Adhesive resins and laminate articles
EP0171626A3 (en) * 1984-07-16 1987-04-29 Nippon Petrochemicals Company, Limited Adhesive resins and laminate articles
US4737548A (en) * 1984-07-16 1988-04-12 Nippon Petrochemicals Adhesive resins and laminate articles

Also Published As

Publication number Publication date
FR1315735A (en) 1963-01-25

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