GB955748A - Improvements relating to polyepoxide resins - Google Patents

Improvements relating to polyepoxide resins

Info

Publication number
GB955748A
GB955748A GB3880361A GB3880361A GB955748A GB 955748 A GB955748 A GB 955748A GB 3880361 A GB3880361 A GB 3880361A GB 3880361 A GB3880361 A GB 3880361A GB 955748 A GB955748 A GB 955748A
Authority
GB
United Kingdom
Prior art keywords
diboron
bis
radical
aromatic hydrocarbon
unsubstituted
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
GB3880361A
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.)
Chemical Corp
US Borax Inc
Original Assignee
Chemical Corp
US Borax 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 Chemical Corp, US Borax Inc filed Critical Chemical Corp
Publication of GB955748A publication Critical patent/GB955748A/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
    • C08G59/4007Curing agents not provided for by the groups C08G59/42 - C08G59/66
    • C08G59/4078Curing agents not provided for by the groups C08G59/42 - C08G59/66 boron containing compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Reinforced Plastic Materials (AREA)
  • Epoxy Resins (AREA)

Abstract

A curable composition comprises a polyepoxide having more than one epoxy group per molecule and 2-50%, based on the weight of the polyepoxide, of an aminodiboron curing agent having one of the following formulae:- <FORM:0955748/C3/1> <FORM:0955748/C3/2> <FORM:0955748/C3/3> where R is H, an unsubstituted saturated aliphatic hydrocarbon radical of 1-12C, an unsubstituted saturated cycloaliphatic hydrocarbon radical of 5-12C, an unsubstituted aromatic hydrocarbon radical, a substituted aromatic hydrocarbon radical having 1 or more aliphatic hydrocarbon substituents of 1-6C, or a substituted aromatic hydrocarbon radical having 1 or more alkoxyl substituents of 1-6C, and R1 and R11, which may be the same or different, are unsubstituted saturated aliphatic hydrocarbon radicals of 1-12C, unsubstituted saturated cycloaliphatic hydrocarbon radicals of 5-12C, unsubstituted aromatic hydrocarbon radicals, substituted aromatic hydrocarbon radicals having 1 or more aliphatic hydrocarbon substituents of 1-6C, or substituted aromatic hydrocarbon radicals having 1 or more alkoxyl substituents of 1-6C, and R111 represents an unsubstituted alkylene radical of 2-3C, a substituted alkylene radical of 2-3C in length having 1 or more aliphatic or aromatic hydrocarbon substituents, an unsubstituted o-phenylene radical or a substituted o-phenylene radical having 1 or more aliphatic hydrocarbon substituents. Long lists of suitable compounds are given of which the following are used in the examples:-a glycidyl polyether derived from epichlorhydrin and bisphenol A, the ester of 2-methyl-4, 5-epoxy-1-hydroxymethyl cyclohexane and 2-methyl-4, 5-epoxy cyclohexane-1-carboxylic acid, an epoxidized polybutadiene, and an epoxidized soya bean oil; tetra-(dimethylamino)diboron, tetra-(anilino) diboron, tetra(n-hexylamino) diboron, sym-bis-(dimethylamino)-diethyldiboron, sym-bis-(diethylamino) diphenyl diboron, sym-bis-(p-toluidino) diisopropyldiboron, sym-bis-(cyclohexylamino) bis-p-ethoxy-phenyl diboron, sym-bis-(cyclohexylamino) bis-(p-ethoxyphenyl) diboron, 2-(1, 3, 2-diazaboximyl)-1, 3, 2-diazaborinane, 2-(1, 3, 2-benzodiazaborolo)-1, 3, 2-benzodiazaborole, and 2-(1, 3-dimethyl-1, 3, 2-diazaborolo)-1, 3-dimethyl-1, 3, 2-diazaborole. Optional additives specified are glass, mineral, and metal fibres, asbestos, mica, iron oxide, bentonite, silica, TiO2 and Cd yellow. Using a mixture of an epoxidized cycloolefinic compound and 15-30% by weight of tetra (anilino) diboron produces on curing with heat a foamed product Ex. 5 illustrates this using the ester of 2-methyl-4, 5-epoxy-1-hydroxymethyl cyclohexane and 2-methyl-4, 5-epoxy cyclohexan-1-carboxylic acid with 20% of tetra (aniline) diboron and curing at 100 DEG C.
GB3880361A 1961-03-06 1961-10-30 Improvements relating to polyepoxide resins Expired GB955748A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US9329361A 1961-03-06 1961-03-06

Publications (1)

Publication Number Publication Date
GB955748A true GB955748A (en) 1964-04-22

Family

ID=22238163

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3880361A Expired GB955748A (en) 1961-03-06 1961-10-30 Improvements relating to polyepoxide resins

Country Status (1)

Country Link
GB (1) GB955748A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5504161A (en) * 1989-04-03 1996-04-02 Reilly Industries, Inc. Vinylpyridine polymer support complexed with boron trifluoride

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5504161A (en) * 1989-04-03 1996-04-02 Reilly Industries, Inc. Vinylpyridine polymer support complexed with boron trifluoride

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