CN1171415A - 带有抑制剂的快速固化的有机硅氧烷组合物 - Google Patents
带有抑制剂的快速固化的有机硅氧烷组合物 Download PDFInfo
- Publication number
- CN1171415A CN1171415A CN97102934A CN97102934A CN1171415A CN 1171415 A CN1171415 A CN 1171415A CN 97102934 A CN97102934 A CN 97102934A CN 97102934 A CN97102934 A CN 97102934A CN 1171415 A CN1171415 A CN 1171415A
- Authority
- CN
- China
- Prior art keywords
- component
- weight
- composition
- weight part
- dimethyl
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 58
- 125000005375 organosiloxane group Chemical group 0.000 title claims abstract description 13
- 239000003112 inhibitor Substances 0.000 title description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims abstract description 51
- 229910052697 platinum Inorganic materials 0.000 claims abstract description 26
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 22
- 239000003054 catalyst Substances 0.000 claims abstract description 18
- -1 thiazolinyl cyclotetrasiloxane Chemical compound 0.000 claims description 89
- 229910052710 silicon Inorganic materials 0.000 claims description 24
- 239000010703 silicon Substances 0.000 claims description 24
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 20
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 18
- 230000003245 working effect Effects 0.000 claims description 13
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 34
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 29
- 229920001296 polysiloxane Polymers 0.000 description 16
- 239000000377 silicon dioxide Substances 0.000 description 14
- 239000001301 oxygen Substances 0.000 description 13
- 229910052760 oxygen Inorganic materials 0.000 description 13
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 13
- 238000010790 dilution Methods 0.000 description 12
- 239000012895 dilution Substances 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 11
- 239000004205 dimethyl polysiloxane Substances 0.000 description 8
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 6
- 239000005977 Ethylene Substances 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 4
- 150000001721 carbon Chemical group 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 125000000962 organic group Chemical group 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- 238000006459 hydrosilylation reaction Methods 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000003060 catalysis inhibitor Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000012763 reinforcing filler Substances 0.000 description 2
- QYLFHLNFIHBCPR-UHFFFAOYSA-N 1-ethynylcyclohexan-1-ol Chemical compound C#CC1(O)CCCCC1 QYLFHLNFIHBCPR-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- JQZGUQIEPRIDMR-UHFFFAOYSA-N 3-methylbut-1-yn-1-ol Chemical compound CC(C)C#CO JQZGUQIEPRIDMR-UHFFFAOYSA-N 0.000 description 1
- 125000006043 5-hexenyl group Chemical group 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CGMFKBXPQJJHBR-UHFFFAOYSA-N [SiH3]O[SiH](C=C)C=C Chemical compound [SiH3]O[SiH](C=C)C=C CGMFKBXPQJJHBR-UHFFFAOYSA-N 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- FSIJKGMIQTVTNP-UHFFFAOYSA-N bis(ethenyl)-methyl-trimethylsilyloxysilane Chemical compound C[Si](C)(C)O[Si](C)(C=C)C=C FSIJKGMIQTVTNP-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- UBHZUDXTHNMNLD-UHFFFAOYSA-N dimethylsilane Chemical compound C[SiH2]C UBHZUDXTHNMNLD-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 235000012204 lemonade/lime carbonate Nutrition 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 150000003057 platinum Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000011218 segmentation Effects 0.000 description 1
- 239000004408 titanium dioxide Substances 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
- 229930195735 unsaturated hydrocarbon Natural products 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
- C08K5/54—Silicon-containing compounds
- C08K5/541—Silicon-containing compounds containing oxygen
- C08K5/5425—Silicon-containing compounds containing oxygen containing at least one C=C bond
-
- 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
- C08G77/06—Preparatory processes
- C08G77/08—Preparatory processes characterised by the catalysts used
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/05—Alcohols; Metal alcoholates
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/610,944 US5629399A (en) | 1996-03-05 | 1996-03-05 | Fast curing organosiloxane compositions with long working times |
| US610,944 | 1996-03-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1171415A true CN1171415A (zh) | 1998-01-28 |
Family
ID=24447025
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN97102934A Pending CN1171415A (zh) | 1996-03-05 | 1997-03-04 | 带有抑制剂的快速固化的有机硅氧烷组合物 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US5629399A (enExample) |
| EP (1) | EP0794217A1 (enExample) |
| JP (1) | JPH09324122A (enExample) |
| KR (1) | KR100459526B1 (enExample) |
| CN (1) | CN1171415A (enExample) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006128338A1 (fr) * | 2005-06-03 | 2006-12-07 | Cen, Jinhe | Fibre synthetique de polymere organosilicique et son procede de fabrication: |
| CN100374525C (zh) * | 2003-03-17 | 2008-03-12 | 陶氏康宁公司 | 具有改进的高温粘结强度的无溶剂硅氧烷压敏粘合剂 |
| CN100379794C (zh) * | 2004-10-27 | 2008-04-09 | 伦斯勒工业学院 | 硅氧烷基聚合物及其组合物、发光装置以及硅氧烷基聚合物用于发光二极管的方法 |
| CN101223476B (zh) * | 2005-06-02 | 2011-11-16 | 道康宁公司 | 纳米图案形成方法，其中所使用的固化抗蚀剂膜和包含该抗蚀剂膜的制品 |
| CN102533214A (zh) * | 2010-11-12 | 2012-07-04 | 信越化学工业株式会社 | 热传导硅脂组合物 |
| WO2012129766A1 (en) * | 2011-03-28 | 2012-10-04 | Henkel (China) Company Limited | Curable silicone resins for led encapsulation |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5880194A (en) * | 1997-09-09 | 1999-03-09 | Dow Corning Corporation | Firewall sealant |
| DE19837855A1 (de) * | 1998-08-20 | 2000-02-24 | Wacker Chemie Gmbh | Härtbare Organopolysiloxanmassen |
| US6573328B2 (en) | 2001-01-03 | 2003-06-03 | Loctite Corporation | Low temperature, fast curing silicone compositions |
| JP5031436B2 (ja) * | 2007-05-08 | 2012-09-19 | モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社 | 低透湿性ポリオルガノシロキサン組成物 |
| US8133423B2 (en) * | 2009-10-20 | 2012-03-13 | The Hong Kong Polytechnic University | Method for fabrication of silicone composite with antimicrobial coating |
| KR20140106744A (ko) * | 2011-12-27 | 2014-09-03 | 다우 코닝 코포레이션 | 규소-결합된 트라이알킬실릴-치환된 유기 기를 포함하는 유기폴리실록산 |
| JP6257906B2 (ja) * | 2013-03-22 | 2018-01-10 | モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社 | 付加硬化型シリコーンゴム組成物 |
| JP6070488B2 (ja) * | 2013-09-05 | 2017-02-01 | 信越化学工業株式会社 | 付加硬化性液状シリコーンゴム組成物及びシリコーンゴム硬化物 |
| CN106928725A (zh) | 2015-12-31 | 2017-07-07 | 蓝星有机硅（上海）有限公司 | 导电的可固化的有机硅橡胶 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2554118B1 (fr) * | 1983-10-26 | 1986-01-17 | Rhone Poulenc Spec Chim | Agent inhibiteur cetonique pour catalyseur d'un metal du groupe du platine et compositions organopolysiloxaniques le contenant |
| JPS60177029A (ja) * | 1984-02-21 | 1985-09-11 | Toray Silicone Co Ltd | オルガノポリシロキサン組成物の硬化方法 |
| US5082894A (en) * | 1990-03-19 | 1992-01-21 | Dow Corning Corporation | Storage stable one-part organosiloxane compositions |
| JP2592021B2 (ja) * | 1992-01-31 | 1997-03-19 | 東レ・ダウコーニング・シリコーン株式会社 | エアーバッグコーティング用液状シリコーンゴム組成物 |
| US5270425A (en) * | 1992-11-23 | 1993-12-14 | Dow Corning Corporation | One-part curable organosiloxane compositions |
| JP2835588B2 (ja) * | 1995-07-31 | 1998-12-14 | 信越化学工業株式会社 | ロール部材用硬化性シリコーンゴム組成物 |
-
1996
- 1996-03-05 US US08/610,944 patent/US5629399A/en not_active Expired - Lifetime
-
1997
- 1997-03-04 EP EP97103561A patent/EP0794217A1/en not_active Withdrawn
- 1997-03-04 KR KR1019970006967A patent/KR100459526B1/ko not_active Expired - Lifetime
- 1997-03-04 CN CN97102934A patent/CN1171415A/zh active Pending
- 1997-03-04 JP JP9048873A patent/JPH09324122A/ja not_active Withdrawn
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100374525C (zh) * | 2003-03-17 | 2008-03-12 | 陶氏康宁公司 | 具有改进的高温粘结强度的无溶剂硅氧烷压敏粘合剂 |
| CN100379794C (zh) * | 2004-10-27 | 2008-04-09 | 伦斯勒工业学院 | 硅氧烷基聚合物及其组合物、发光装置以及硅氧烷基聚合物用于发光二极管的方法 |
| CN101223476B (zh) * | 2005-06-02 | 2011-11-16 | 道康宁公司 | 纳米图案形成方法，其中所使用的固化抗蚀剂膜和包含该抗蚀剂膜的制品 |
| US8691389B2 (en) | 2005-06-02 | 2014-04-08 | Dow Corning Corporation | Method of nanopatterning, a cured resist film use therein, and an article including the resist film |
| WO2006128338A1 (fr) * | 2005-06-03 | 2006-12-07 | Cen, Jinhe | Fibre synthetique de polymere organosilicique et son procede de fabrication: |
| CN102533214A (zh) * | 2010-11-12 | 2012-07-04 | 信越化学工业株式会社 | 热传导硅脂组合物 |
| CN102533214B (zh) * | 2010-11-12 | 2015-02-18 | 信越化学工业株式会社 | 热传导硅脂组合物 |
| WO2012129766A1 (en) * | 2011-03-28 | 2012-10-04 | Henkel (China) Company Limited | Curable silicone resins for led encapsulation |
| US8668991B2 (en) | 2011-03-28 | 2014-03-11 | Henkel (China) Company Limited | Curable resins for LED encapsulation |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0794217A1 (en) | 1997-09-10 |
| KR100459526B1 (ko) | 2005-04-13 |
| KR970065645A (ko) | 1997-10-13 |
| US5629399A (en) | 1997-05-13 |
| JPH09324122A (ja) | 1997-12-16 |
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| SE01 | Entry into force of request for substantive examination | ||
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |