GB1106083A - Copolymers - Google Patents

Copolymers

Info

Publication number
GB1106083A
GB1106083A GB2869364A GB2869364A GB1106083A GB 1106083 A GB1106083 A GB 1106083A GB 2869364 A GB2869364 A GB 2869364A GB 2869364 A GB2869364 A GB 2869364A GB 1106083 A GB1106083 A GB 1106083A
Authority
GB
United Kingdom
Prior art keywords
copolymer
groups
ratio
copolymers
transfer agent
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
GB2869364A
Inventor
Kenneth Robert Smith
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.)
Coates Brothers and Co Ltd
Original Assignee
Coates Brothers and Co 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 Coates Brothers and Co Ltd filed Critical Coates Brothers and Co Ltd
Priority to GB2869364A priority Critical patent/GB1106083A/en
Publication of GB1106083A publication Critical patent/GB1106083A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/62Monocarboxylic acids having ten or more carbon atoms; Derivatives thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)

Abstract

A copolymer is made from (A) a compound containing an epoxide ring and copolymerizable double bond, (B) an alpha-beta unsaturated carboxylic acid, and (c) a vinyl or vinylidene monomer or mixture of monomers free from epoxide groups, active-hydrogen containing groups, and nitrile groups, the ratio of epoxy to carboxy groups in the copolymer being between 1:6 and 6:1 and the ratio of the sum of the weights of (A) and (B) to the total monomer weight being not greater than 1:2 and not less than 1:5, the molecular weight and gel content of which copolymer have been limited through the presence during the formation of the copolymer of a chain transfer agent. The polymerization is suitably carried out using a free radical initiator. The copolymers may be cured by moderate heat, suitably in the presence of a catalyst such as a tertiary amine. In the Examples, copolymers of (1-3) methyl methacrylate, n-butyl acrylate, glycidyl methacrylate and acrylic acid, (4) methyl and n-butyl methacrylates, glycidyl methacrylate and methacrylic acid, (5) n-butyl acrylate, methyl methacrylate, glycidyl acrylate and acrylic acid, and (6) methyl methacrylate, n-butyl acrylate, allyl-9:10-epoxystearate, and acrylic acid are prepared using methyl ethyl ketone peroxide as initiator, ethylene glycol monoethyl ether as solvent, and dodecyl mercaptan as chain transfer agent. The resulting copolymers are formed into solutions in a xylol/butanol mixture and mixed with TiO2.ALSO:A curable coating comprises a copolymer made from (A) a compound containing an epoxide ring and copolymerisable double bond, (B) an alpha-beta unsaturated carboxylic acid, and (C) a vinyl or vinylidene monomer or mixture of monomers free from epoxide groups, active-hydrogen containing groups, and nitrile groups, the ratio of epoxy to carboxy groups in the copolymer being between 1:6 and 6:1 and the ratio of the sum of the weights of (A) and (B) to the total monomer weight being not greater than 1:2 and not less than 1:5, the molecular weight and gel content of which copolymer have been limited through the presence during the formation of the copolymer of a chain transfer agent. The coatings may also include a pigment such as TiO2, and may be cured by moderate heat under force-drying conditions using a catalyst, suitably a tertiary amine. The coating of glass plates and aluminium panels is exemplified.
GB2869364A 1964-07-10 1964-07-10 Copolymers Expired GB1106083A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2869364A GB1106083A (en) 1964-07-10 1964-07-10 Copolymers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2869364A GB1106083A (en) 1964-07-10 1964-07-10 Copolymers

Publications (1)

Publication Number Publication Date
GB1106083A true GB1106083A (en) 1968-03-13

Family

ID=10279607

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2869364A Expired GB1106083A (en) 1964-07-10 1964-07-10 Copolymers

Country Status (1)

Country Link
GB (1) GB1106083A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3689592A (en) * 1969-12-08 1972-09-05 Goldschmidt Ag Th Heat-hardenable, foil containing polymerizate with pendent glycidyl groups

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3689592A (en) * 1969-12-08 1972-09-05 Goldschmidt Ag Th Heat-hardenable, foil containing polymerizate with pendent glycidyl groups

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