GB906544A - - Google Patents
Info
- 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
- Authority
- GB
- United Kingdom
- Prior art keywords
- silicone
- delta
- bis
- radical
- units
- 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.)
- Active
Links
- 229920001296 polysiloxane Polymers 0.000 abstract 6
- 150000003377 silicon compounds Chemical class 0.000 abstract 6
- -1 hydrocarbon radical Chemical class 0.000 abstract 4
- 239000007795 chemical reaction product Substances 0.000 abstract 3
- 229920002545 silicone oil Polymers 0.000 abstract 3
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000005840 aryl radicals Chemical group 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 229920000647 polyepoxide Polymers 0.000 abstract 2
- 150000003254 radicals Chemical class 0.000 abstract 2
- 239000013638 trimer Substances 0.000 abstract 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 abstract 1
- OECTYKWYRCHAKR-UHFFFAOYSA-N 4-vinylcyclohexene dioxide Chemical compound C1OC1C1CC2OC2CC1 OECTYKWYRCHAKR-UHFFFAOYSA-N 0.000 abstract 1
- ZFIVKAOQEXOYFY-UHFFFAOYSA-N Diepoxybutane Chemical compound C1OC1C1OC1 ZFIVKAOQEXOYFY-UHFFFAOYSA-N 0.000 abstract 1
- 239000007983 Tris buffer Substances 0.000 abstract 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical group C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- BQQUFAMSJAKLNB-UHFFFAOYSA-N dicyclopentadiene diepoxide Chemical compound C12C(C3OC33)CC3C2CC2C1O2 BQQUFAMSJAKLNB-UHFFFAOYSA-N 0.000 abstract 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 1
- MYRTYDVEIRVNKP-UHFFFAOYSA-N divinylbenzene Substances C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 235000011187 glycerol Nutrition 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
- DENFJSAFJTVPJR-UHFFFAOYSA-N triethoxy(ethyl)silane Chemical compound CCO[Si](CC)(OCC)OCC DENFJSAFJTVPJR-UHFFFAOYSA-N 0.000 abstract 1
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates 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
- C08G59/18—Macromolecules 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
- C08G59/40—Macromolecules 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
- C08G59/50—Amines
- C08G59/5046—Amines heterocyclic
- C08G59/5053—Amines heterocyclic containing only nitrogen as a heteroatom
- C08G59/508—Amines heterocyclic containing only nitrogen as a heteroatom having three nitrogen atoms in the ring
- C08G59/5086—Triazines; Melamines; Guanamines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates 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
- C08G59/18—Macromolecules 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
- C08G59/40—Macromolecules 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
- C08G59/50—Amines
- C08G59/504—Amines containing an atom other than nitrogen belonging to the amine group, carbon and hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
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)
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.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB906544A true GB906544A (en) |
Family
ID=1753305
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB906544D Active GB906544A (en) |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB906544A (en) |
Cited By (5)
| 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 |
-
0
- GB GB906544D patent/GB906544A/en active Active
Cited By (9)
| 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 a secondary amine-terminated siloxane modifier |
| 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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