NO317290B1 - Tverrbindbare blandinger og fremgangsmater for fremstilling av disse - Google Patents
Tverrbindbare blandinger og fremgangsmater for fremstilling av disse Download PDFInfo
- Publication number
- NO317290B1 NO317290B1 NO19993163A NO993163A NO317290B1 NO 317290 B1 NO317290 B1 NO 317290B1 NO 19993163 A NO19993163 A NO 19993163A NO 993163 A NO993163 A NO 993163A NO 317290 B1 NO317290 B1 NO 317290B1
- Authority
- NO
- Norway
- Prior art keywords
- component
- mixture according
- crosslinkable mixture
- crosslinkable
- components
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 40
- 238000000034 method Methods 0.000 title claims description 4
- 238000002360 preparation method Methods 0.000 title description 2
- -1 polysiloxane Polymers 0.000 claims description 20
- 239000003112 inhibitor Substances 0.000 claims description 14
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 14
- 229920001296 polysiloxane Polymers 0.000 claims description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
- 229910052710 silicon Inorganic materials 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 6
- 229910052697 platinum Inorganic materials 0.000 claims description 5
- 229920002554 vinyl polymer Polymers 0.000 claims description 5
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 4
- 238000006459 hydrosilylation reaction Methods 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 239000010703 silicon Substances 0.000 claims description 2
- 150000002903 organophosphorus compounds Chemical class 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229920002379 silicone rubber Polymers 0.000 description 3
- 239000004945 silicone rubber Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 2
- 125000005624 silicic acid group Chemical class 0.000 description 2
- 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 1
- 125000006039 1-hexenyl group Chemical group 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229910002621 H2PtCl6 Inorganic materials 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- UIEXFJVOIMVETD-UHFFFAOYSA-N P([O-])([O-])[O-].[Pt+3] Chemical class P([O-])([O-])[O-].[Pt+3] UIEXFJVOIMVETD-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 229910003930 SiCb Inorganic materials 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910020447 SiO2/2 Inorganic materials 0.000 description 1
- 229910020487 SiO3/2 Inorganic materials 0.000 description 1
- WYUIWUCVZCRTRH-UHFFFAOYSA-N [[[ethenyl(dimethyl)silyl]amino]-dimethylsilyl]ethene Chemical compound C=C[Si](C)(C)N[Si](C)(C)C=C WYUIWUCVZCRTRH-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910021502 aluminium hydroxide Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 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
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-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
- 150000001721 carbon Chemical group 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000000460 chlorine Chemical group 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 229910001679 gibbsite Inorganic materials 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910052909 inorganic silicate Inorganic materials 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 125000002347 octyl 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])[H] 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004344 phenylpropyl group Chemical group 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 150000003057 platinum Chemical class 0.000 description 1
- 150000003058 platinum compounds Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002510 pyrogen Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 125000000725 trifluoropropyl group Chemical group [H]C([H])(*)C([H])([H])C(F)(F)F 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
- C08K5/526—Esters of phosphorous acids, e.g. of H3PO3 with hydroxyaryl compounds
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Silicon Polymers (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Insulating Materials (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19654690 | 1996-12-30 | ||
| PCT/EP1997/007084 WO1998029497A1 (de) | 1996-12-30 | 1997-12-17 | Vernetzbare mischungen und ein verfahren zu deren herstellung |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO993163L NO993163L (no) | 1999-06-25 |
| NO993163D0 NO993163D0 (no) | 1999-06-25 |
| NO317290B1 true NO317290B1 (no) | 2004-10-04 |
Family
ID=7816401
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19993163A NO317290B1 (no) | 1996-12-30 | 1999-06-25 | Tverrbindbare blandinger og fremgangsmater for fremstilling av disse |
Country Status (20)
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU741611B2 (en) * | 1996-12-30 | 2001-12-06 | Ge Bayer Silicones Gmbh & Co. Kg | Cross-linkable mixtures and method for producing same |
| EP1499660A2 (fr) * | 2002-04-29 | 2005-01-26 | Rhodia Chimie | Ensemble catalytique pour hydrosilylation, son procede de preparation et compositions silicone l incorporant |
| FR2838985B1 (fr) * | 2002-04-29 | 2005-03-18 | Rhodia Chimie Sa | Ensemble catalytique pour hydrosilylation et compositions silicone l'incorporant |
| FR2847900B1 (fr) * | 2002-12-02 | 2006-06-09 | Rhodia Chimie Sa | Ensemble catalytique pour hydrosilylation, son procede de preparation et composition silicone l'incorporant |
| FR2848215B1 (fr) * | 2002-12-04 | 2006-08-04 | Rhodia Chimie Sa | Composition elastomere silicone, adhesive, monocomposante et reticulable par polyaddition |
| US7067570B2 (en) * | 2002-12-10 | 2006-06-27 | Shin-Etsu Chemical Co., Ltd. | One-part organopolysiloxane gel composition |
| JP4530147B2 (ja) * | 2004-08-25 | 2010-08-25 | 信越化学工業株式会社 | 一液型オルガノポリシロキサンゲル組成物 |
| US8318831B2 (en) * | 2005-06-22 | 2012-11-27 | 3M Innovative Properties Company | Hydrophilized curable silicone impression materials with improved storage behavior |
| DE102006016753A1 (de) | 2006-04-10 | 2007-10-11 | Wacker Chemie Ag | Vernetzbare Massen auf der Basis von Organosiliciumverbindungen |
| JP2007308581A (ja) * | 2006-05-18 | 2007-11-29 | Shin Etsu Chem Co Ltd | 付加硬化型シリコーンゴム組成物の硬化方法及び付加硬化型シリコーンゴム組成物 |
| DE102007047212A1 (de) * | 2007-10-02 | 2009-04-09 | Wacker Chemie Ag | Härtbare Siliconzusammensetzungen |
| JP2009091403A (ja) * | 2007-10-04 | 2009-04-30 | Shin Etsu Chem Co Ltd | 付加硬化型シリコーンゴム組成物及びその硬化方法 |
| JP2009220384A (ja) * | 2008-03-17 | 2009-10-01 | Shin Etsu Chem Co Ltd | シリコーンゴム薄膜被覆層の形成方法、及びシリコーンゴム薄膜被覆物品 |
| WO2010009755A1 (en) * | 2008-07-21 | 2010-01-28 | Momentive Performance Materials Gmbh | Curable silicone compositions comprising aryl-phosphites |
| EP2613942A1 (fr) | 2010-09-06 | 2013-07-17 | Bluestar Silicones France | Rouleau compressible pour imprimante |
| US9549881B2 (en) | 2013-02-25 | 2017-01-24 | 3M Innovative Properties Company | Stabilized dental impression composition, kit of parts and use thereof |
| TW201625754A (zh) * | 2014-11-21 | 2016-07-16 | 艾倫塔斯有限公司 | 單一成份、儲存穩定、可硬化之聚矽氧組成物 |
| CN114174436B (zh) * | 2019-07-25 | 2023-09-01 | 信越化学工业株式会社 | 单组分型固化性有机硅凝胶组合物和有机硅凝胶固化物 |
| JP2025518040A (ja) | 2022-05-25 | 2025-06-12 | モメンティブ パフォーマンス マテリアルズ ゲーエムベーハー | 新規な置換ホスファイト遷移金属化合物 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5950256B2 (ja) * | 1979-07-27 | 1984-12-07 | 東芝シリコ−ン株式会社 | 硬化性ポリシロキサン組成物 |
| US5036117A (en) * | 1989-11-03 | 1991-07-30 | Dow Corning Corporation | Heat-curable silicone compositions having improved bath life |
| US5380812A (en) * | 1994-01-10 | 1995-01-10 | Dow Corning Corporation | One part curable compositions containing deactivated hydrosilation catalyst and method for preparing same |
| DE19532316C1 (de) * | 1995-09-01 | 1997-05-22 | Bayer Ag | Vernetzbare Polysiloxan-Mischungen, ein Verfahren zur Herstellung und deren Verwendung |
| AU741611B2 (en) * | 1996-12-30 | 2001-12-06 | Ge Bayer Silicones Gmbh & Co. Kg | Cross-linkable mixtures and method for producing same |
-
1997
- 1997-12-17 AU AU56637/98A patent/AU741611B2/en not_active Expired
- 1997-12-17 US US09/319,846 patent/US6300455B1/en not_active Expired - Lifetime
- 1997-12-17 PL PL97334880A patent/PL189704B1/pl unknown
- 1997-12-17 SK SK893-99A patent/SK89399A3/sk unknown
- 1997-12-17 CA CA002276010A patent/CA2276010A1/en not_active Abandoned
- 1997-12-17 BR BR9714444A patent/BR9714444A/pt not_active Application Discontinuation
- 1997-12-17 SI SI9720092A patent/SI20077A/sl not_active IP Right Cessation
- 1997-12-17 JP JP52957998A patent/JP4181639B2/ja not_active Expired - Lifetime
- 1997-12-17 WO PCT/EP1997/007084 patent/WO1998029497A1/de active IP Right Grant
- 1997-12-17 IL IL13046697A patent/IL130466A0/xx unknown
- 1997-12-17 DE DE59710143T patent/DE59710143D1/de not_active Expired - Lifetime
- 1997-12-17 AT AT97952952T patent/ATE240987T1/de not_active IP Right Cessation
- 1997-12-17 HU HU0000784A patent/HUP0000784A3/hu unknown
- 1997-12-17 ID IDW990604A patent/ID22339A/id unknown
- 1997-12-17 KR KR1019997005912A patent/KR20000069773A/ko not_active Withdrawn
- 1997-12-17 TR TR1999/01506T patent/TR199901506T2/xx unknown
- 1997-12-17 EP EP97952952A patent/EP0948565B1/de not_active Expired - Lifetime
- 1997-12-17 ES ES97952952T patent/ES2200214T3/es not_active Expired - Lifetime
- 1997-12-29 ZA ZA9711636A patent/ZA9711636B/xx unknown
-
1999
- 1999-06-25 NO NO19993163A patent/NO317290B1/no not_active IP Right Cessation
-
2008
- 2008-02-04 JP JP2008023873A patent/JP2008189928A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| AU741611B2 (en) | 2001-12-06 |
| AU5663798A (en) | 1998-07-31 |
| PL334880A1 (en) | 2000-03-27 |
| PL189704B1 (pl) | 2005-09-30 |
| IL130466A0 (en) | 2000-06-01 |
| HUP0000784A2 (en) | 2000-07-28 |
| TR199901506T2 (xx) | 1999-09-21 |
| HUP0000784A3 (en) | 2001-02-28 |
| EP0948565A1 (de) | 1999-10-13 |
| WO1998029497A1 (de) | 1998-07-09 |
| ES2200214T3 (es) | 2004-03-01 |
| DE59710143D1 (de) | 2003-06-26 |
| EP0948565B1 (de) | 2003-05-21 |
| BR9714444A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2000-03-21 |
| ID22339A (id) | 1999-09-30 |
| SI20077A (sl) | 2000-04-30 |
| ZA9711636B (en) | 1998-07-08 |
| ATE240987T1 (de) | 2003-06-15 |
| JP4181639B2 (ja) | 2008-11-19 |
| NO993163L (no) | 1999-06-25 |
| CA2276010A1 (en) | 1998-07-09 |
| KR20000069773A (ko) | 2000-11-25 |
| JP2008189928A (ja) | 2008-08-21 |
| NO993163D0 (no) | 1999-06-25 |
| SK89399A3 (en) | 2000-01-18 |
| US6300455B1 (en) | 2001-10-09 |
| JP2001508096A (ja) | 2001-06-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO317290B1 (no) | Tverrbindbare blandinger og fremgangsmater for fremstilling av disse | |
| KR101610964B1 (ko) | 액상 경화성 플루오로실리콘 조성물의 탈포성을 향상시키는 방법 | |
| JP5603837B2 (ja) | 付加硬化型シリコーン組成物及び光学素子 | |
| GB1562993A (en) | Organosiloxane composition for liquid injection moulding | |
| JP5835100B2 (ja) | 帯電防止性シリコーンゴム組成物及び帯電防止性シリコーンゴム硬化物の黄変を抑制する方法 | |
| AU716990B2 (en) | Crosslinkable mixtures, a method of preparing them and their use | |
| US6346562B1 (en) | Cross-linkable mixtures and a method for the production and utilization thereof | |
| EP2221343A1 (en) | Thermocurable silicone rubber composition | |
| JP2519563B2 (ja) | オルガノポリシロキサン組成物及びその硬化物 | |
| JP6006632B2 (ja) | 付加硬化型シリコーン組成物及び光学素子 | |
| US6566430B2 (en) | Curable organopolysiloxane compositions | |
| US5240984A (en) | Silicon rubber composition | |
| EP2639273B1 (en) | Silicone Rubber Composition | |
| JP3829933B2 (ja) | 難燃性シリコーン組成物 | |
| JP3384861B2 (ja) | 導電性シリコーンゴム組成物およびその製造方法 | |
| JP3521590B2 (ja) | 付加反応用触媒組成物及び硬化性オルガノポリシロキサン組成物 | |
| JP3644488B2 (ja) | オイルブリード性シリコーンゴム組成物 | |
| EP3770219B1 (en) | Silicone gel composition, cured product thereof, and power module | |
| CZ238699A3 (cs) | Zesíťovatelné směsi a způsob jejich výroby | |
| JP2025074893A (ja) | ミラブル型シリコーンゴム組成物及びその硬化物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK1K | Patent expired |