GB897726A - A process for the manufacture of hardened artificial resin materials and compositions therefor - Google Patents

A process for the manufacture of hardened artificial resin materials and compositions therefor

Info

Publication number
GB897726A
GB897726A GB27256/58A GB2725658A GB897726A GB 897726 A GB897726 A GB 897726A GB 27256/58 A GB27256/58 A GB 27256/58A GB 2725658 A GB2725658 A GB 2725658A GB 897726 A GB897726 A GB 897726A
Authority
GB
United Kingdom
Prior art keywords
acrylamide
acid
copolymerization
cyclohexyl
butyl
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
GB27256/58A
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.)
BASF Schweiz AG
Original Assignee
Ciba AG
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 Ciba AG filed Critical Ciba AG
Publication of GB897726A publication Critical patent/GB897726A/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
    • 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L57/00Compositions of unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2363/00Characterised by the use of epoxy resins; Derivatives of epoxy resins

Abstract

A hardenable composition comprises an epoxy resin which is substantially free from carboxyl groups and contains n epoxide groups calculated on the molecular weight, where n represents a whole or fractional number greater than 1, and a copolymerization product obtained by polymerizing at least one compound containing at least one polymerizable carbon-to-carbon double bond and at least one tertiary amino group of the formula -NR1R2 in which R1 and R2 each represent a hydrocarbon radical of 1 to 6 carbon atoms which may be substituted or may be linked together to form with the nitrogen atom a heterocyclic ring, jointly with at least one non-basic amide of a copolymerizable acid, and the content of the component containing a tertiary amino group in the copolymerization product being less than 40% by weight. As materials containing basic tertiary amino groups there are suitable such compounds as are specified for the copolymer curing agents of Specification 897,985. As copolymerizable non-basic amides there are specified amides of acryl, methacrylic fumaric and crotonic acids, e.g. N-methyl ethyl butyl ter. octyl- and cyclohexyl acrylamides, N,N-dimethyl or dibutyl acrylamides or methacrylamides, N;N-di(b -hydroxyethyl)acrylamide, N-cyclohexyl-N-2-hydroxypropylacrylamide and hexamethylolmelamine triacrylic acid amide. The copolymers may also contain a third copolymerization component such as a vinyl ester, vinyl halide, vinyl alkyl ketone, vinylaryl compound, esters of acrylic acid, methacrylic, a -chloracrylic, crotonic, itaconic, maleic or fumaric acids, acrylic acid itself or polymerizable olefins. The copolymers may be used together with such compounds as triethylene tetramine, N:N-diethylpropylene diamine, tris-(dimethylaminomethyl)phenol, 4,41-diaminodiphenylmethane, phthalic, tetrahydrophthalic or hexahydrophthalic anhydride, methylendomethylenetetrahydrophthalic anhydride or hexachloroendomethylene-tetrahydrophthalic anhydride. As modifiers there can be added to the compositions epoxy-dodecane, hexadecane or octadecane or epoxidized fatty acids or fatty acid esters. Plasticizers such as dibutyl phthalate and extenders such as quartz powder, kaolin, stone powder, glass or asbestos fibres may be added. For use in treating leather, paper or textiles the compositions may be used in the form of an emulsion, for example, with hydrolyzed PVA, propylene glycol alginate and a nonyl-phenol/ethylene oxide reaction product. In the examples the copolymerization products obtained from (1) N-diethylaminopropylacrylamide, N-tertiary butyl acrylamide and ethyl acrylate; (2) N-tert.-octylacrylamide and N-diethylaminophenyl acrylamide; (3) N-dimethylaminoethyl vinyl ether; (4) N-diethylaminoethyl crotonate, butyl methacrylate and di-butyl acrylamide; (5) N-diethylaminopropyl acrylamide, N-cyclohexyl-N-(2-hydroxypropyl)-acrylamide, and isobutyl acrylate; (6) diethylaminopropyl acrylamide and hexamethylolmelamine triacrylic acid amide. Epoxy resins employed are the polyglycidyl ethers of 4,41-dihydroxydiphenyl dimethyl methane, ethylene glycol, butylene glycol; reaction products of epichlorhydrin with terephthalic acid, a phenolformaldehyde novolak or aniline. Specification 816,630 also is referred to.
GB27256/58A 1957-08-23 1958-08-25 A process for the manufacture of hardened artificial resin materials and compositions therefor Expired GB897726A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH4975557 1957-08-23

Publications (1)

Publication Number Publication Date
GB897726A true GB897726A (en) 1962-05-30

Family

ID=4516795

Family Applications (2)

Application Number Title Priority Date Filing Date
GB27256/58A Expired GB897726A (en) 1957-08-23 1958-08-25 A process for the manufacture of hardened artificial resin materials and compositions therefor
GB27255/58A Expired GB897985A (en) 1957-08-23 1958-08-25 A process for the manufacture of hardened artificial resin materials and compositions therefor

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB27255/58A Expired GB897985A (en) 1957-08-23 1958-08-25 A process for the manufacture of hardened artificial resin materials and compositions therefor

Country Status (6)

Country Link
BE (2) BE570570A (en)
CH (1) CH49755A (en)
DE (2) DE1085667B (en)
FR (2) FR1211575A (en)
GB (2) GB897726A (en)
NL (5) NL6408445A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3385809A (en) * 1965-09-03 1968-05-28 Richardson Co Fat acid amides of nu, nu-dialkyl (alkylene diamines) as curing agents for epoxy resi
US3538185A (en) * 1967-08-10 1970-11-03 Dow Chemical Co Coating compositions containing vinyl polymers with pendant alkylenimine group and epoxy resins

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1120133B (en) * 1959-01-23 1961-12-21 Ciba Geigy Process for accelerating the hardening of polyepoxy compounds by means of anhydride polybasic carboxylic acids
US3467611A (en) * 1966-01-07 1969-09-16 Du Pont Mixture of aqueous emulsions
JPS5428960B1 (en) * 1968-01-22 1979-09-20
GB1555781A (en) * 1975-08-27 1979-11-14 Pollution Preventing Res Methods for producing dibasic fatty acid
CA1086445A (en) * 1976-02-23 1980-09-23 Changkiu K. Riew Thermoplastic, thermosetting elastomeric compositions and methods for making the same
US4889890A (en) * 1987-12-30 1989-12-26 Ppg Industries, Inc. Powder coating curing system containing a beta-hydroxyalkylamide
US5013791A (en) * 1987-12-30 1991-05-07 Ppg Industries, Inc. Beta-hydroxyalkylamide cured acid polymer/polyepoxide powder coating
EP3118234A1 (en) 2015-07-15 2017-01-18 ALLNEX AUSTRIA GmbH Coating compositions

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3385809A (en) * 1965-09-03 1968-05-28 Richardson Co Fat acid amides of nu, nu-dialkyl (alkylene diamines) as curing agents for epoxy resi
US3538185A (en) * 1967-08-10 1970-11-03 Dow Chemical Co Coating compositions containing vinyl polymers with pendant alkylenimine group and epoxy resins

Also Published As

Publication number Publication date
NL6408449A (en) 1964-10-12
NL230770A (en)
BE570570A (en)
FR1211576A (en) 1960-03-17
DE1106492B (en) 1961-05-10
FR1211575A (en) 1960-03-17
NL6408445A (en) 1964-10-12
NL110442C (en)
CH49755A (en) 1911-03-16
BE570571A (en)
NL110443C (en)
DE1085667B (en) 1960-07-21
GB897985A (en) 1962-06-06

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