GB844978A - Improvements in or relating to the curing of glycidyl polyethers - Google Patents

Improvements in or relating to the curing of glycidyl polyethers

Info

Publication number
GB844978A
GB844978A GB3463/58A GB346358A GB844978A GB 844978 A GB844978 A GB 844978A GB 3463/58 A GB3463/58 A GB 3463/58A GB 346358 A GB346358 A GB 346358A GB 844978 A GB844978 A GB 844978A
Authority
GB
United Kingdom
Prior art keywords
polymers
styrene
vinyl
vinyl acetate
homopolymers
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
GB3463/58A
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.)
Celanese Coatings Co Inc
Original Assignee
Devoe and Raynolds Co Inc
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 Devoe and Raynolds Co Inc filed Critical Devoe and Raynolds Co Inc
Publication of GB844978A publication Critical patent/GB844978A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins

Landscapes

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

Abstract

A glycidyl polyether containing more than one epoxide group per molecule and having a weight per epoxide below 1,000 is reacted with a polybasic acid anhydride and a polyhydroxy polymer containing 0,5 to 25% by weight of hydroxyl groups selected from alkenol homopolymers, hydrolised alkenyl alkanoate homopolymers, hydroxy alkyl alkenoate homopolymers and co-polymers of monomers of said homopolymers with vinyl compounds containing a single polymerizable H2C=C < group, where the anhydride and the glycidyl polyether are used in an equivalent ratio of 0,5 to 1 to 4:1 and polymer is used in an amount of from 0,5 to 80% by weight of the composition. Specified glycidyl polyethers include those made by reacting polyhydric alcohols or phenols e.g. resorcinol, hydroquinone, bis-phenol, catechol and glycerol with epihalohydrins e.g. 3-chloro-1, 2-epoxybutane, 3-bromo-1, 2-epoxyhexane and 3-chloro-1, 2-epoxyoctane or glycidyl polyethers. Specified polybasic acid anhydrides include succinic, maleic, pyromellitic, Chlorendic and Nadic anhydrides. Specified polyhydroxy polymers include co-polymers of allyl alcohol with styrene, vinylidene chloride, acrylonitrile and methallyl chloride, hydrolised polyvinyl acetate and hydrolised co-polymers of ethylene chloride and vinyl acetate, vinyl acetate and vinyl chloride, methyl methacrylate and vinyl acetate and vinyl acetate and styrene. The reaction may be effected in a solvent e.g. p acetone, methyl ethyl ketone, methyl isobutyl ketone, di-isobutyl ketone, "Cellosolve" (Registered Trade Mark) acetate and mixtures thereof with xylene, toluene or benzene. Catalysts specified for the reaction are tertiary amines, amine salts or quaternary ammonium hydroxides and peroxide or hydroperoxide polymerization catalysts. Exemplified glycidyl polyethers are made from bis-phenol or resorcinol and epichlorohydrin. Exemplified polyhydroxy polymers are copolymers of styrene and hydroxypropyl acrylate, terpolymers of styrene, methyl acrylate and hydroxy propyl acrylate, co-polymers of vinyl toluene and hydroxypropyl acrylate, co-polymers of vinyl toluene and hydroxypropyl methacrylate, co-polymers of styrene and the acrylic acid ester of phenyl glycidyl ether and co-polymers of vinyl acetate and hydroxypropyl crotonate. U.S.A. Specifications 2,581,464, 2,582,985, 2,615,007 and 2,615,008 are referred to.
GB3463/58A 1957-03-21 1958-02-03 Improvements in or relating to the curing of glycidyl polyethers Expired GB844978A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US844978XA 1957-03-21 1957-03-21

Publications (1)

Publication Number Publication Date
GB844978A true GB844978A (en) 1960-08-17

Family

ID=22185333

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3463/58A Expired GB844978A (en) 1957-03-21 1958-02-03 Improvements in or relating to the curing of glycidyl polyethers

Country Status (1)

Country Link
GB (1) GB844978A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2148900A (en) * 1983-08-19 1985-06-05 Ici Plc Curable compositions
EP0225097A2 (en) * 1985-11-25 1987-06-10 E.I. Du Pont De Nemours And Company Two component coating composition of an anhydride containing polymer and a glycidyl component

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2148900A (en) * 1983-08-19 1985-06-05 Ici Plc Curable compositions
EP0225097A2 (en) * 1985-11-25 1987-06-10 E.I. Du Pont De Nemours And Company Two component coating composition of an anhydride containing polymer and a glycidyl component
EP0225097A3 (en) * 1985-11-25 1988-01-27 E.I. Du Pont De Nemours And Company Two component coating composition of an anhydride containing polymer and a glycidyl component
JPH0749551B2 (en) 1985-11-25 1995-05-31 イー・アイ・デュポン・ドゥ・ヌムール・アンド・カンパニー Coating composition

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