NO312905B1 - Herdbare organopolysiloksanmasser, platinakatalysatorer anvendt i disse, og anvendelse av de herdbareorganopolysiloksanmasser - Google Patents
Herdbare organopolysiloksanmasser, platinakatalysatorer anvendt i disse, og anvendelse av de herdbareorganopolysiloksanmasser Download PDFInfo
- Publication number
- NO312905B1 NO312905B1 NO19994965A NO994965A NO312905B1 NO 312905 B1 NO312905 B1 NO 312905B1 NO 19994965 A NO19994965 A NO 19994965A NO 994965 A NO994965 A NO 994965A NO 312905 B1 NO312905 B1 NO 312905B1
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- Norway
- Prior art keywords
- residues
- carbon
- platinum
- cyclooctadiene
- residue
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- 229920001296 polysiloxane Polymers 0.000 title claims abstract description 88
- 239000003054 catalyst Substances 0.000 title claims abstract description 61
- 229910052697 platinum Inorganic materials 0.000 title claims abstract description 53
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 26
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- 150000001875 compounds Chemical class 0.000 claims abstract description 20
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- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 10
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- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 claims abstract description 6
- 150000001993 dienes Chemical class 0.000 claims abstract description 6
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 3
- -1 siloxane residues Chemical group 0.000 claims description 81
- 239000000203 mixture Substances 0.000 claims description 37
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 22
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- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 claims description 11
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- BBDKZWKEPDTENS-UHFFFAOYSA-N 4-Vinylcyclohexene Chemical compound C=CC1CCC=CC1 BBDKZWKEPDTENS-UHFFFAOYSA-N 0.000 description 1
- INYHZQLKOKTDAI-UHFFFAOYSA-N 5-ethenylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=C)CC1C=C2 INYHZQLKOKTDAI-UHFFFAOYSA-N 0.000 description 1
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 1
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- WSTYNZDAOAEEKG-UHFFFAOYSA-N Mayol Natural products CC1=C(O)C(=O)C=C2C(CCC3(C4CC(C(CC4(CCC33C)C)=O)C)C)(C)C3=CC=C21 WSTYNZDAOAEEKG-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229910020487 SiO3/2 Inorganic materials 0.000 description 1
- 229910008338 Si—(CH3) Inorganic materials 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001345 alkine derivatives Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- 229940045985 antineoplastic platinum compound Drugs 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- FSIJKGMIQTVTNP-UHFFFAOYSA-N bis(ethenyl)-methyl-trimethylsilyloxysilane Chemical group C[Si](C)(C)O[Si](C)(C=C)C=C FSIJKGMIQTVTNP-UHFFFAOYSA-N 0.000 description 1
- ZPOLOEWJWXZUSP-AATRIKPKSA-N bis(prop-2-enyl) (e)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C\C(=O)OCC=C ZPOLOEWJWXZUSP-AATRIKPKSA-N 0.000 description 1
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
- JKJWYKGYGWOAHT-UHFFFAOYSA-N bis(prop-2-enyl) carbonate Chemical compound C=CCOC(=O)OCC=C JKJWYKGYGWOAHT-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 1
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cis-cyclohexene Natural products C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- CHVJITGCYZJHLR-UHFFFAOYSA-N cyclohepta-1,3,5-triene Chemical compound C1C=CC=CC=C1 CHVJITGCYZJHLR-UHFFFAOYSA-N 0.000 description 1
- UVJHQYIOXKWHFD-UHFFFAOYSA-N cyclohexa-1,4-diene Chemical compound C1C=CCC=C1 UVJHQYIOXKWHFD-UHFFFAOYSA-N 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000004386 diacrylate group Chemical group 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 description 1
- LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 description 1
- UOUILILVWRHZSH-UHFFFAOYSA-N dimethyl-tris[(dimethyl-$l^{3}-silanyl)oxy]silyloxysilicon Chemical compound C[Si](C)O[Si](O[Si](C)C)(O[Si](C)C)O[Si](C)C UOUILILVWRHZSH-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- NFWSQSCIDYBUOU-UHFFFAOYSA-N methylcyclopentadiene Chemical compound CC1=CC=CC1 NFWSQSCIDYBUOU-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- DYUWTXWIYMHBQS-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCNCC=C DYUWTXWIYMHBQS-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 description 1
- 125000003518 norbornenyl group Chemical group C12(C=CC(CC1)C2)* 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 229910000064 phosphane Inorganic materials 0.000 description 1
- 150000003002 phosphanes Chemical class 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000004447 silicone coating Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- JFLKFZNIIQFQBS-FNCQTZNRSA-N trans,trans-1,4-Diphenyl-1,3-butadiene Chemical compound C=1C=CC=CC=1\C=C\C=C\C1=CC=CC=C1 JFLKFZNIIQFQBS-FNCQTZNRSA-N 0.000 description 1
- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- IYQYZZHQSZMZIG-UHFFFAOYSA-N tricyclo[5.2.1.0(2.6)]deca-3,8-diene, 4.9-dimethyl Chemical compound C1C2C3C=C(C)CC3C1C=C2C IYQYZZHQSZMZIG-UHFFFAOYSA-N 0.000 description 1
- UHUUYVZLXJHWDV-UHFFFAOYSA-N trimethyl(methylsilyloxy)silane Chemical compound C[SiH2]O[Si](C)(C)C UHUUYVZLXJHWDV-UHFFFAOYSA-N 0.000 description 1
- OVFFWUHKSNMAOJ-UHFFFAOYSA-N tris(ethenyl)-[ethenyl(dimethyl)silyl]oxysilane Chemical group C=C[Si](C)(C)O[Si](C=C)(C=C)C=C OVFFWUHKSNMAOJ-UHFFFAOYSA-N 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0091—Complexes with metal-heteroatom-bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0086—Platinum compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/12—Polysiloxanes containing silicon bound to hydrogen
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Silicon Polymers (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19847097A DE19847097A1 (de) | 1998-10-13 | 1998-10-13 | Härtbare Organopolysiloxanmassen |
Publications (3)
Publication Number | Publication Date |
---|---|
NO994965D0 NO994965D0 (no) | 1999-10-12 |
NO994965L NO994965L (no) | 2000-04-14 |
NO312905B1 true NO312905B1 (no) | 2002-07-15 |
Family
ID=7884278
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO19994965A NO312905B1 (no) | 1998-10-13 | 1999-10-12 | Herdbare organopolysiloksanmasser, platinakatalysatorer anvendt i disse, og anvendelse av de herdbareorganopolysiloksanmasser |
Country Status (8)
Country | Link |
---|---|
US (1) | US6252028B1 (da) |
EP (1) | EP0994159B1 (da) |
JP (1) | JP3190646B2 (da) |
AT (1) | ATE200301T1 (da) |
CA (1) | CA2285913C (da) |
DE (2) | DE19847097A1 (da) |
DK (1) | DK0994159T3 (da) |
NO (1) | NO312905B1 (da) |
Families Citing this family (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5057413B2 (ja) * | 1999-08-03 | 2012-10-24 | 東レ・ダウコーニング株式会社 | 有機架橋粒子、そのサスペンジョン、およびそれらの製造方法 |
DE19938338A1 (de) * | 1999-08-13 | 2001-02-22 | Wacker Chemie Gmbh | Härtbare Organopolysiloxanmassen |
DE10062181A1 (de) * | 2000-12-14 | 2002-07-04 | Wacker Chemie Gmbh | Härtbare Organopolysiloxanmassen |
US7026480B2 (en) * | 2001-03-08 | 2006-04-11 | The University Of Hong Kong | Organometallic light-emitting material |
DE10121513A1 (de) | 2001-05-03 | 2002-11-14 | Wacker Chemie Gmbh | Hochviskose alkenyl-terminierte Polydiorganosiloxane enthaltende additionsvernetzbare Siliconmassen |
GB0112525D0 (en) * | 2001-05-23 | 2001-07-11 | Dow Corning | Polysiloxanes and gels and pastes containing them |
DE10214137A1 (de) | 2002-03-28 | 2003-10-16 | Wacker Chemie Gmbh | Siliconmassen mit verbesserter Hitzestabilität |
US6660396B1 (en) | 2002-06-03 | 2003-12-09 | Truseal Usa, Inc. | Molded encapsulated indicia system |
DE10242798A1 (de) * | 2002-09-14 | 2004-04-01 | Degussa Ag | Silikonkautschuk |
DE502004000039D1 (de) | 2003-07-04 | 2005-09-15 | Wacker Chemie Gmbh | Lagerstabile Siliconmassen |
DE102004050128A1 (de) * | 2004-10-14 | 2006-04-20 | Wacker Chemie Ag | Siliconkautschuk Zusammensetzung mit verbesserter Haltbarkeit |
DE102004050129A1 (de) * | 2004-10-14 | 2006-04-20 | Wacker Chemie Ag | Siliconkautschuk Zusammensetzung enthaltend unbehandeltes Aluminiumhydroxid als Füllstoff |
DE102004060934A1 (de) * | 2004-12-17 | 2006-06-29 | Wacker Chemie Ag | Vernetzbare Polyorganosiloxanmassen |
DE102005022106A1 (de) | 2005-05-12 | 2006-11-16 | Wacker Chemie Ag | Hochviskose Polydiorganosiloxane enthaltende additionsvernetzbare Siliconmassen |
DE102007007569A1 (de) | 2007-02-15 | 2008-08-21 | Wacker Chemie Ag | Additionsvernetzbare Siliconmassen mit geringen Reibungskoeffizienten |
DE102007047212A1 (de) | 2007-10-02 | 2009-04-09 | Wacker Chemie Ag | Härtbare Siliconzusammensetzungen |
DE102008041940A1 (de) * | 2008-09-10 | 2010-03-11 | Wacker Chemie Ag | Siliconelastomere mit verbesserter Einreissfestigkeit |
DE102009027847A1 (de) | 2009-07-20 | 2011-01-27 | Wacker Chemie Ag | Härtbare Siliconzusammensetzungen |
DE102010039085A1 (de) * | 2010-08-09 | 2012-02-09 | Wacker Chemie Ag | Selbsthaftende Siliconelastomere |
KR20140041578A (ko) * | 2011-06-29 | 2014-04-04 | 다우 코닝 코포레이션 | 하이드로실릴화 반응 경화성 조성물 및 그의 제조 및 사용 방법 |
DE102011088146A1 (de) | 2011-12-09 | 2013-07-25 | Wacker Chemie Ag | Zu Elastomeren vernetzbare Siliconmasse mit einvernetzbaren Polyglykolethern |
DE102012213260A1 (de) | 2012-07-27 | 2014-01-30 | Wacker Chemie Ag | Additionsvernetzende Siliconzusammensetzung mit niedrigem Druckverformungsrest |
DE102014203613A1 (de) * | 2014-02-27 | 2015-08-27 | Wacker Chemie Ag | Additionsvernetzende Siliconzusammensetzung mit hohem Wasseraufnahmevermögen |
CN106715536B (zh) | 2014-09-19 | 2021-06-01 | 莫门蒂夫性能材料股份有限公司 | 用于受控的硅氧烷交联的铂(ii)二烯配合物 |
JP7107636B2 (ja) | 2015-01-22 | 2022-07-27 | モーメンティブ・パフォーマンス・マテリアルズ・インク | シクロジエン添加剤を使用する白金触媒ヒドロシリル化反応 |
CN111032741A (zh) | 2017-08-04 | 2020-04-17 | 瓦克化学股份公司 | 贵金属催化剂的稳定化 |
CN108359242A (zh) * | 2018-02-24 | 2018-08-03 | 江苏燕园精英医疗科技有限公司 | 一种透明硅橡胶印膜材料及制备方法 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4329275A (en) | 1979-07-27 | 1982-05-11 | Toshiba Silicone Co., Ltd. | Heat-curable polysiloxane composition |
US4603215A (en) * | 1984-08-20 | 1986-07-29 | Dow Corning Corporation | Platinum (O) alkyne complexes |
US4645815A (en) | 1985-10-31 | 1987-02-24 | General Electric Company | Heat curable organopolysiloxane compositions |
EP0363006A3 (en) | 1988-09-02 | 1991-01-09 | Dow Corning Corporation | A method for curing storage stable organosiloxane compositions containing microencapsulated ingredients |
DE3906514A1 (de) * | 1989-03-01 | 1990-09-06 | Consortium Elektrochem Ind | Cycloolefinkomplexe des platins, verfahren zu deren herstellung sowie deren verwendung als katalysator |
JPH089006B2 (ja) * | 1989-11-15 | 1996-01-31 | 信越化学工業株式会社 | 白金触媒組成物及びその製造方法 |
US5122585A (en) * | 1990-12-10 | 1992-06-16 | General Electric Company | One part heat curable organopolysiloxane compositions |
JPH06157912A (ja) * | 1992-08-13 | 1994-06-07 | General Electric Co <Ge> | 一液型熱硬化性オルガノポリシロキサン組成物の製法 |
US5328974A (en) * | 1993-05-06 | 1994-07-12 | Wacker Silicones Corporation | Platinum catalyst and a curable organopolysiloxane composition containing said platinum catalyst |
KR950003310A (ko) * | 1993-07-22 | 1995-02-16 | 에리히 프랑크, 칼-하인즈 림뵉 | 균질 히드로실릴화 촉매 |
CA2128342C (en) | 1993-07-22 | 1997-06-24 | Jochen Dauth | Organosilicon compounds having triazene groups |
DE4429411A1 (de) * | 1994-08-19 | 1996-02-22 | Wacker Chemie Gmbh | Verfahren zur Herstellung von Metallkomplexen der 8. Nebengruppe und deren Verwednung in vernetzbaren Organopolysiloxanmassen |
-
1998
- 1998-10-13 DE DE19847097A patent/DE19847097A1/de not_active Withdrawn
-
1999
- 1999-09-09 DK DK99117453T patent/DK0994159T3/da active
- 1999-09-09 DE DE59900064T patent/DE59900064D1/de not_active Expired - Lifetime
- 1999-09-09 AT AT99117453T patent/ATE200301T1/de not_active IP Right Cessation
- 1999-09-09 EP EP99117453A patent/EP0994159B1/de not_active Expired - Lifetime
- 1999-10-07 US US09/414,351 patent/US6252028B1/en not_active Expired - Lifetime
- 1999-10-12 JP JP29014599A patent/JP3190646B2/ja not_active Expired - Lifetime
- 1999-10-12 NO NO19994965A patent/NO312905B1/no unknown
- 1999-10-13 CA CA002285913A patent/CA2285913C/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
ATE200301T1 (de) | 2001-04-15 |
JP2000198850A (ja) | 2000-07-18 |
EP0994159B1 (de) | 2001-04-04 |
DK0994159T3 (da) | 2001-07-23 |
NO994965D0 (no) | 1999-10-12 |
CA2285913A1 (en) | 2000-04-13 |
CA2285913C (en) | 2005-08-16 |
EP0994159A1 (de) | 2000-04-19 |
JP3190646B2 (ja) | 2001-07-23 |
DE59900064D1 (de) | 2001-05-10 |
NO994965L (no) | 2000-04-14 |
DE19847097A1 (de) | 2000-04-20 |
US6252028B1 (en) | 2001-06-26 |
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