GB906544A - - Google Patents

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Publication number
GB906544A
GB906544A GB906544DA GB906544A GB 906544 A GB906544 A GB 906544A GB 906544D A GB906544D A GB 906544DA GB 906544 A GB906544 A GB 906544A
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United Kingdom
Prior art keywords
silicone
delta
bis
radical
units
Prior art date
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Publication of GB906544A publication Critical patent/GB906544A/en
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    • 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
    • C08G59/50Amines
    • C08G59/5046Amines heterocyclic
    • C08G59/5053Amines heterocyclic containing only nitrogen as a heteroatom
    • C08G59/508Amines heterocyclic containing only nitrogen as a heteroatom having three nitrogen atoms in the ring
    • C08G59/5086Triazines; Melamines; Guanamines
    • 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
    • C08G59/50Amines
    • C08G59/504Amines containing an atom other than nitrogen belonging to the amine group, carbon and hydrogen
    • 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

Abstract

906,544. Polyepoxide-organo-polysiloxane reaction products. UNION CARBIDE CORPORATION. Oct. 20, 1958 [Oct. 21, 1957], No. 33348/58. Classes 2(5) and 2(7) The Specification discloses the reaction product of a polyepoxide with an organofunctional silicon compound of the formula where R and R<SP>1</SP> are hydrogen or a monovalent hydrocarbon radical, R<SP>11</SP> is a divalent hydrocarbon group, R<SP>111</SP> is a monovalent hydrocarbon group, n is an integer of at least 2, a is an integer of from 1 to 3, b is 0, 1 or 2 and the sum of a and b is not greater than 3, c is 0, 1 or 2, x and y are molecular fractions indicating the molecular proportions of their respective units in the compound and x+y is 1, Q is an alkyl or aryl radical or the radical where G is hydrogen or an alkyl or aryl radical and m is an integer of from 1 to 4 and X represents the radical or with a mixture of one or more such organofunctional silicon compounds, or with a mixture of one or more such organofunctional silicon compounds with an oxygen containing silicon compound of the general formula where Y is a hydroxy, hydroxy substituted hydrocarbon or 0¢. Many organofunctional silicon compounds are specified, examples being 3:5-diaminotriazinylaminopropyltriethoxysilane, 3 :S-dibutylaminotriazinylaminopropyl triethoxysilane, #-(m-aminophenyl) ethyl triethoxysilane, γ(3:5-dimethylaminophenyl)propylphenyldiethoxysilane and N-(yaminopropyl)-delta-aminobutyltriethoxysilane. The siloxanes derived from the organofunctional silicon compounds may be employed. Specified polyepoxides are butadiene dioxide, vinylcyclohexene dioxide, dicyclopentadiene dioxide, diglycidyl ether, the triglycidyl ether of glycerine, 3:4-epoxycyclohexylmethyl, 3:4-epoxycyclohexanecarboxylate, 1:6-hexanediol bis(3:4-epoxycyclohexane carboxylate), 1:1:1 -trimethylol propane tris(3:4-epoxycyclohexanecarboxylate), bis (3:4-epoxy-6-methylcyclohexylmethyl) maleate, bis(2:3-epoxycyclopentyl)ether, divinyl benzene dioxide and the di- and polyglycidyl ethers of 4:41-dihydroxydipheylpropane and 4:4<SP>1</SP>-dihydroxy-diphenyl methane. The examples describe the preparation of reaction products from the diglycidyl of bis-phenol-A and:-(1) a silicone oil containing gammacyanopropylmethyl silicone and delta-aminobutylmethylsilicone units; (2) #-m-aminophenylethylmethyl silicone cyclic trimer and tetramer; (3) a dimethyl silicone oil containing #-m-aminophenylethylmethyl silicone units; (4) a dimethyl silicone oil containing N,3:5-diaminotriazinyl-delta-aminobutyl-methyl silicone units; (5) N,γ-aminopropol-delta-aminobutyl methyl silicone cyclic trimer and tetramer; (6) m-aminophenylethyl methylsilicone oil and (7) γ-aminopropyltriethoxysilane. Specifications 795,894, 882,051, 882,053, 882,054, 882,062, 882,094, 882,095, 882,096, 882,097 and 882,103 are referred to.
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0218228A2 (en) 1985-10-07 1987-04-15 Shin-Etsu Chemical Co., Ltd. Epoxy resin composition
EP0312771A1 (en) * 1987-09-24 1989-04-26 BASF Aktiengesellschaft Thermosetting resin systems containing secondary amine-terminated siloxane modifiers
US5006614A (en) * 1988-07-05 1991-04-09 Shin-Etsu Chemical Co., Ltd. Epoxy resin composition and semiconductor device encapsulated therewith containing polymaleimide and (allyl-epoxy)novolac/siloxane graft copolymer
DE4025215A1 (en) * 1990-08-09 1992-02-13 Fraunhofer Ges Forschung METHOD FOR PRODUCING AN ALKALISTABLE AND ABRASION RESISTANT COATING AND LACQUER FOR USE IN THIS METHOD
US5393859A (en) * 1993-06-07 1995-02-28 Ciba-Geigy Corporation Organopolysiloxanes containing substituted 1,3,5-triazine units

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0218228A2 (en) 1985-10-07 1987-04-15 Shin-Etsu Chemical Co., Ltd. Epoxy resin composition
EP0218228A3 (en) * 1985-10-07 1989-05-24 Shin-Etsu Chemical Co., Ltd. Epoxy resin composition
US4877822A (en) * 1985-10-07 1989-10-31 Shin-Etsu Chemical Co., Ltd. Epoxy resin composition
US5053445A (en) * 1985-10-07 1991-10-01 Shin-Etsu Chemical Co., Ltd. Epoxy resin composition
EP0312771A1 (en) * 1987-09-24 1989-04-26 BASF Aktiengesellschaft Thermosetting resin systems containing secondary amine-terminated siloxane modifiers
JPH02269159A (en) * 1987-09-24 1990-11-02 Basf Corp Thermosetting resin system containing modifier comprising siloxane having terminal secondary amine group
US5006614A (en) * 1988-07-05 1991-04-09 Shin-Etsu Chemical Co., Ltd. Epoxy resin composition and semiconductor device encapsulated therewith containing polymaleimide and (allyl-epoxy)novolac/siloxane graft copolymer
DE4025215A1 (en) * 1990-08-09 1992-02-13 Fraunhofer Ges Forschung METHOD FOR PRODUCING AN ALKALISTABLE AND ABRASION RESISTANT COATING AND LACQUER FOR USE IN THIS METHOD
US5393859A (en) * 1993-06-07 1995-02-28 Ciba-Geigy Corporation Organopolysiloxanes containing substituted 1,3,5-triazine units

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