GB855025A - Improvements in and relating to polymerisable epoxide compositions - Google Patents

Improvements in and relating to polymerisable epoxide compositions

Info

Publication number
GB855025A
GB855025A GB3250658A GB3250658A GB855025A GB 855025 A GB855025 A GB 855025A GB 3250658 A GB3250658 A GB 3250658A GB 3250658 A GB3250658 A GB 3250658A GB 855025 A GB855025 A GB 855025A
Authority
GB
United Kingdom
Prior art keywords
acid
anhydride
mixtures
anhydrides
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
GB3250658A
Inventor
Benjamin Phillips
Charles Wesley Mcgary Jnr
Charles Theo Patrick Jnr
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 GB3250658A priority Critical patent/GB855025A/en
Publication of GB855025A publication Critical patent/GB855025A/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
    • 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
    • C08G59/20Macromolecules 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 epoxy compounds used
    • C08G59/22Di-epoxy compounds
    • C08G59/24Di-epoxy compounds carbocyclic
    • C08G59/245Di-epoxy compounds carbocyclic aromatic
    • 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)
  • Epoxy Resins (AREA)
  • Epoxy Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A polymerizable composition comprises o, m or p-divinyl benzene dioxide and a polycarboxylic acid anhydride in an amount having 0,2 to 3 carboxyl equivalents per epoxy group; a polycarboxylic acid compound may also be present in amount having up to 1 carboxyl group per epoxy group, the total number not exceeding 3 and the acid always providing fewer carboxyl equivalents than the anhydride. The compositions are converted to hard, infusible resins by heating to 25 to 250 DEG C., if desired in the presence of catalysts. The polycarboxylic anhydrides may be of the formula XCO.O.CO, where X is 2 or more carbon atoms connected by single or double bonds and which may contain hydroxyl, nitro, chloro, iodo, bromo, and cyclic groups, as well as interconnecting oxydicarbonyl groups. Mixtures of anhydrides may be used. Many examples are given. The poly carboxylic acids are of the same classes and the acid compounds include poylhydric alcohol esters which contain more than one carboxyl group per molecule. The catalysts include mineral acids, sulphuric acids, metal halide Lewis acids, alkali metal hydroxides and amines, including aminophenols. They may be added as solutions in organic solvents. The uncured or partially cured compositions may be dissolved in solvents, e.g. xylene, methyl isobutyl ketone, butyl, ethyl and amyl acetates and toluene, particularly for applying surface coatings which are subsequently heat cured. In the examples, the dioxides are mixtures of the three isomers containing ethyl styrene oxide as main impurity. The hardeners are phthalic, succinic, glutonic, polyadipic and chlorendic anhydrides, mixtures of phthalic anhydric and sebacic acid, maleic anhydride and adipic acid, polyadipic anhydride and maleic acid, and of glutaric acid and the adduct of 1 mol of glycerol with 3 mols of succinic anhydride.
GB3250658A 1958-10-11 1958-10-11 Improvements in and relating to polymerisable epoxide compositions Expired GB855025A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3250658A GB855025A (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
GB3250658A GB855025A (en) 1958-10-11 1958-10-11 Improvements in and relating to polymerisable epoxide compositions

Publications (1)

Publication Number Publication Date
GB855025A true GB855025A (en) 1960-11-30

Family

ID=10339646

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3250658A Expired GB855025A (en) 1958-10-11 1958-10-11 Improvements in and relating to polymerisable epoxide compositions

Country Status (1)

Country Link
GB (1) GB855025A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011103014A1 (en) 2010-02-19 2011-08-25 Dow Global Technologies Llc Divinylarene dioxide resin compositions
WO2011146580A2 (en) 2010-05-21 2011-11-24 Dow Global Technologies Llc Curable compositions
CN102432835A (en) * 2010-06-29 2012-05-02 陶氏环球技术有限公司 Curable compositions
WO2012158291A1 (en) * 2011-05-13 2012-11-22 Dow Global Technologies Llc Insulation formulations

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011103014A1 (en) 2010-02-19 2011-08-25 Dow Global Technologies Llc Divinylarene dioxide resin compositions
US9359468B2 (en) 2010-02-19 2016-06-07 Blue Cube Ip Llc Divinylarene dioxide resin compositions
WO2011146580A2 (en) 2010-05-21 2011-11-24 Dow Global Technologies Llc Curable compositions
WO2011146580A3 (en) * 2010-05-21 2012-04-05 Dow Global Technologies Llc Curable compositions
RU2581832C2 (en) * 2010-05-21 2016-04-20 БЛЮ КЬЮБ АйПи ЭлЭлСи Curable compositions
CN102432835A (en) * 2010-06-29 2012-05-02 陶氏环球技术有限公司 Curable compositions
WO2012158291A1 (en) * 2011-05-13 2012-11-22 Dow Global Technologies Llc Insulation formulations
JP2014520172A (en) * 2011-05-13 2014-08-21 ダウ グローバル テクノロジーズ エルエルシー Insulation compound

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