GB866410A - Improvements in and relating to polymerisable epoxide compositions - Google Patents

Improvements in and relating to polymerisable epoxide compositions

Info

Publication number
GB866410A
GB866410A GB3250558A GB3250558A GB866410A GB 866410 A GB866410 A GB 866410A GB 3250558 A GB3250558 A GB 3250558A GB 3250558 A GB3250558 A GB 3250558A GB 866410 A GB866410 A GB 866410A
Authority
GB
United Kingdom
Prior art keywords
acid
anhydride
polycarboxylic
mixture
acids
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
GB3250558A
Inventor
Benjamin Phillips
Charles Wesley Mcgary
Charles Theo Patrick
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
Priority to GB3250558A priority Critical patent/GB866410A/en
Publication of GB866410A publication Critical patent/GB866410A/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
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/42Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof

Landscapes

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

Abstract

A polymerizable composition comprises divinylbenzene dioxide and a polycarboxylic acid compound in an amount having 0,3 to 1,25 carboxyl equivalents per epoxy equivalent; the composition may also contain a lesser amount of a polycarboxylic acid anhydride to the extent of 0,75 carboxyl equivalents per epoxy equivalent, the total number of carboxyl equivalents per epoxy equivalent being not greater than 1,25 The cured resins have the recurring units:- <FORM:0866410/IV (a)/1> where Y is a polycarboxylic acid residue. Any of the o, m, or p-isomers of divinylbenzene dioxide, or mixtures thereof, may be used. Suitable polycarboxylic acids include saturated and unsaturated di- and tri-carboxylic acids. These may be wholly or partly replaced by polycarboxy polyesters prepared from polyhydric alcohols and excess polycarboxylic acid. The polyhydric alcohols include glycols, oxyalkylene glycols, alkane diols, tri- and tetra-hydric and higher polyhydric alcohols, polyvinyl alcohol, and epoxide reaction products. Examples are given of polycarboxylic acid anhydrides which may be used; these may also be saturated or unsaturated and include acid dianhydrides. Acid catalysts may be added to the compositions, e.g. mineral acids, sulphonic acid and metal halide Lewis acids, and they may be in form of solutions in organic solvents. The uncured or partially cured compositions may be dissolved in solvents such as xylene, methyl isobutyl ketone, ethyl-, butyl- and amyl-acetate and toluene, and applied as a coating composition which is subsequently completely cured. The examples specify the following polycarboxylic compounds: adipic acid, an adduct of succinic anhydride (3 mols) with glycerol (1 mol), glutaric acid, an adduct of phthalic anhydride (2 mols) with ethylene glycol (1 mol), sebacic acid, a mixture of adipic acid and phthalic anhydride, a mixture of sebacic acid and maleic anhydride, a mixture of maleic acid and glutaric anhydride, a mixture of methyltetrahydrophthalic anhydride and an adduct of glycerol and succinic anhydride. Also given for comparison are benzoic, acetic and butyric acids.
GB3250558A 1958-10-11 1958-10-11 Improvements in and relating to polymerisable epoxide compositions Expired GB866410A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3250558A GB866410A (en) 1958-10-11 1958-10-11 Improvements in and relating to polymerisable epoxide compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3250558A GB866410A (en) 1958-10-11 1958-10-11 Improvements in and relating to polymerisable epoxide compositions

Publications (1)

Publication Number Publication Date
GB866410A true GB866410A (en) 1961-04-26

Family

ID=10339627

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3250558A Expired GB866410A (en) 1958-10-11 1958-10-11 Improvements in and relating to polymerisable epoxide compositions

Country Status (1)

Country Link
GB (1) GB866410A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5034473A (en) * 1989-08-17 1991-07-23 National Starch And Chemical Investment Holding Company Composition of polyepoxide derived from alkoxy-substituted allylphenol and carboxy-terminated polyester or polyamide
US20120220750A1 (en) * 2009-12-08 2012-08-30 Dow Global Technologies Llc Hydroxyl-functional polyester resins

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5034473A (en) * 1989-08-17 1991-07-23 National Starch And Chemical Investment Holding Company Composition of polyepoxide derived from alkoxy-substituted allylphenol and carboxy-terminated polyester or polyamide
US20120220750A1 (en) * 2009-12-08 2012-08-30 Dow Global Technologies Llc Hydroxyl-functional polyester resins
US8975343B2 (en) * 2009-12-08 2015-03-10 Dow Global Technologies Llc Hydroxyl-functional polyester resins

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