TWI462970B - 室溫下可固化之有機聚矽氧烷組合物 - Google Patents
室溫下可固化之有機聚矽氧烷組合物 Download PDFInfo
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- TWI462970B TWI462970B TW097137994A TW97137994A TWI462970B TW I462970 B TWI462970 B TW I462970B TW 097137994 A TW097137994 A TW 097137994A TW 97137994 A TW97137994 A TW 97137994A TW I462970 B TWI462970 B TW I462970B
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- 239000000203 mixture Substances 0.000 title claims abstract description 108
- 229920001296 polysiloxane Polymers 0.000 title claims abstract description 8
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000010936 titanium Substances 0.000 claims abstract description 12
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 6
- 239000003054 catalyst Substances 0.000 claims abstract description 6
- 239000013522 chelant Substances 0.000 claims abstract description 6
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 3
- 150000002430 hydrocarbons Chemical group 0.000 claims description 14
- 229910000420 cerium oxide Inorganic materials 0.000 claims description 9
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- 239000000758 substrate Substances 0.000 abstract description 14
- 229920005645 diorganopolysiloxane polymer Polymers 0.000 abstract 1
- 125000005369 trialkoxysilyl group Chemical group 0.000 abstract 1
- 239000011521 glass Substances 0.000 description 14
- -1 trimethoxysulfanyl group Chemical group 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 9
- 238000002955 isolation Methods 0.000 description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- YTPFRRRNIYVFFE-UHFFFAOYSA-N 2,2,3,3,5,5-hexamethyl-1,4-dioxane Chemical compound CC1(C)COC(C)(C)C(C)(C)O1 YTPFRRRNIYVFFE-UHFFFAOYSA-N 0.000 description 6
- GCZWJRLXIPVNLU-UHFFFAOYSA-N 2,2-dimethoxy-3-methylundecane Chemical compound CC(C(OC)(OC)C)CCCCCCCC GCZWJRLXIPVNLU-UHFFFAOYSA-N 0.000 description 6
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 description 6
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 238000000576 coating method Methods 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 239000000565 sealant Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 240000004307 Citrus medica Species 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 description 4
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 4
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 4
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 4
- FCHAHVALRSEXTN-UHFFFAOYSA-N CC(CCCC(CCCC)(OCC)OCC)C Chemical compound CC(CCCC(CCCC)(OCC)OCC)C FCHAHVALRSEXTN-UHFFFAOYSA-N 0.000 description 3
- MMJGHBIXGOTKRR-UHFFFAOYSA-N [Ti].C(C)CC#N.C(C)CC#N Chemical compound [Ti].C(C)CC#N.C(C)CC#N MMJGHBIXGOTKRR-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000004888 barrier function Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- LNEJJQMNHUGXDW-UHFFFAOYSA-N CC(C(OCC)(OCC)C)CCCCCCCC Chemical compound CC(C(OCC)(OCC)C)CCCCCCCC LNEJJQMNHUGXDW-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 238000004382 potting Methods 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- OTGGHZUEAWMAAK-UHFFFAOYSA-N (1,1-dimethoxy-1-phenyldecan-2-yl)benzene Chemical compound C1(=CC=CC=C1)C(C(OC)(OC)C1=CC=CC=C1)CCCCCCCC OTGGHZUEAWMAAK-UHFFFAOYSA-N 0.000 description 1
- JPEWDCTZJFUITH-UHFFFAOYSA-N 1-methoxydecane Chemical compound CCCCCCCCCCOC JPEWDCTZJFUITH-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- VOQDCMULDZDDLP-UHFFFAOYSA-N 2-methoxy-2,3-dimethyloxane Chemical compound CC1C(OCCC1)(C)OC VOQDCMULDZDDLP-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-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
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- AUJBNJFBJPKHPY-UHFFFAOYSA-N 4,4-diethoxy-5-methyltridecane Chemical compound CC(C(OCC)(OCC)CCC)CCCCCCCC AUJBNJFBJPKHPY-UHFFFAOYSA-N 0.000 description 1
- UAPJIXSMWIFQEH-UHFFFAOYSA-N 4,4-dimethoxy-5-methyltridecane Chemical compound CC(C(OC)(OC)CCC)CCCCCCCC UAPJIXSMWIFQEH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- DPDVAQUTUAZEKP-UHFFFAOYSA-N C(=C)C(C(OC)(OC)C=C)CCCCCCCC Chemical compound C(=C)C(C(OC)(OC)C=C)CCCCCCCC DPDVAQUTUAZEKP-UHFFFAOYSA-N 0.000 description 1
- CAPXJNGJKLJAKM-UHFFFAOYSA-N C(=C)C(C(OCC)(OCC)C=C)CCCCCCCC Chemical compound C(=C)C(C(OCC)(OCC)C=C)CCCCCCCC CAPXJNGJKLJAKM-UHFFFAOYSA-N 0.000 description 1
- QNGUFVBAHBNZGW-UHFFFAOYSA-N C(C)C(C(OC)(OC)CC)CCCCCCCC Chemical compound C(C)C(C(OC)(OC)CC)CCCCCCCC QNGUFVBAHBNZGW-UHFFFAOYSA-N 0.000 description 1
- XEPAKJGFUVCJOW-UHFFFAOYSA-N C(C)C(C(OCC)(OCC)CC)CCCCCCCC Chemical compound C(C)C(C(OCC)(OCC)CC)CCCCCCCC XEPAKJGFUVCJOW-UHFFFAOYSA-N 0.000 description 1
- GHDHVFYKUQKSRV-UHFFFAOYSA-N C(C1=CC=CC=C1)C(CCCCCCCCC)(OC)OC Chemical compound C(C1=CC=CC=C1)C(CCCCCCCCC)(OC)OC GHDHVFYKUQKSRV-UHFFFAOYSA-N 0.000 description 1
- RPLANZPCJBROPJ-UHFFFAOYSA-N C(C1=CC=CC=C1)C(CCCCCCCCC)(OCC)OCC Chemical compound C(C1=CC=CC=C1)C(CCCCCCCCC)(OCC)OCC RPLANZPCJBROPJ-UHFFFAOYSA-N 0.000 description 1
- STJBWPMXSJHEFV-UHFFFAOYSA-N C1(=CC=CC=C1)C(C(OCC)(OCC)C1=CC=CC=C1)CCCCCCCC Chemical compound C1(=CC=CC=C1)C(C(OCC)(OCC)C1=CC=CC=C1)CCCCCCCC STJBWPMXSJHEFV-UHFFFAOYSA-N 0.000 description 1
- GGGZEAQPQFUYCJ-UHFFFAOYSA-N CC(C(OC)(OC)CC)CCCCCCCC Chemical compound CC(C(OC)(OC)CC)CCCCCCCC GGGZEAQPQFUYCJ-UHFFFAOYSA-N 0.000 description 1
- QTBITDQOMQRBCU-UHFFFAOYSA-N CC(C(OCC)(OCC)CC)CCCCCCCC Chemical compound CC(C(OCC)(OCC)CC)CCCCCCCC QTBITDQOMQRBCU-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical group CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- PYHNCTSVRKZVJY-UHFFFAOYSA-N [Ti].CC(C)=NO.CC(C)=NO Chemical compound [Ti].CC(C)=NO.CC(C)=NO PYHNCTSVRKZVJY-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000003342 alkenyl group Chemical group 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
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 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
- RXKUYBRRTKRGME-UHFFFAOYSA-N butanimidamide Chemical compound CCCC(N)=N RXKUYBRRTKRGME-UHFFFAOYSA-N 0.000 description 1
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 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
- 125000002704 decyl 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])* 0.000 description 1
- 229940008099 dimethicone Drugs 0.000 description 1
- 125000001891 dimethoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000008393 encapsulating agent Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000006038 hexenyl group Chemical group 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000001624 naphthyl group Chemical group 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
- 239000003960 organic solvent Substances 0.000 description 1
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer 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
- 230000009974 thixotropic effect Effects 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000000725 trifluoropropyl group Chemical group [H]C([H])(*)C([H])([H])C(F)(F)F 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- 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
- 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
- C08L83/06—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- 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
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
- C08G77/18—Polysiloxanes containing silicon bound to oxygen-containing groups to alkoxy or aryloxy groups
-
- 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
- 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
- C08K5/5415—Silicon-containing compounds containing oxygen containing at least one Si—O bond
- C08K5/5419—Silicon-containing compounds containing oxygen containing at least one Si—O bond containing at least one Si—C bond
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- 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)
- Paints Or Removers (AREA)
- Sealing Material Composition (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007278105A JP5285892B2 (ja) | 2007-10-25 | 2007-10-25 | 室温硬化性オルガノポリシロキサン組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW200932833A TW200932833A (en) | 2009-08-01 |
| TWI462970B true TWI462970B (zh) | 2014-12-01 |
Family
ID=40279059
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW097137994A TWI462970B (zh) | 2007-10-25 | 2008-10-02 | 室溫下可固化之有機聚矽氧烷組合物 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8247516B2 (https=) |
| EP (1) | EP2207856B1 (https=) |
| JP (1) | JP5285892B2 (https=) |
| KR (1) | KR101528789B1 (https=) |
| CN (1) | CN101827905B (https=) |
| AT (1) | ATE548432T1 (https=) |
| TW (1) | TWI462970B (https=) |
| WO (1) | WO2009054279A1 (https=) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR112012005909A2 (pt) | 2009-09-15 | 2020-08-25 | Basf Se | compostos do catalisador de quelato de ti, formulação de catalisador de quelato de ti, uso do composto de catalisador de quelato de ti, ou da formulação de catalisador de quelato de ti, composição polimerizável, processo para a polimerização de compostos, uso da composição polimerizável, substrato revestido, e, composição polimerizada ou reticulada |
| US10207261B2 (en) | 2009-09-15 | 2019-02-19 | Basf Se | Photo-latent titanium catalysts |
| DE102010041676A1 (de) * | 2010-09-29 | 2012-03-29 | Wacker Chemie Ag | Vernetzbare Organopolysiloxanzusammensetzung |
| JP2012158619A (ja) * | 2011-01-28 | 2012-08-23 | Dow Corning Toray Co Ltd | プライマー用組成物及び積層体 |
| RU2610090C9 (ru) | 2011-04-05 | 2018-04-26 | Басф Се | Фотолатентные катализаторы на основе титан-оксо-хелатов |
| CN109563347A (zh) * | 2016-08-19 | 2019-04-02 | 道康宁东丽株式会社 | 用于保护电气/电子部件的室温可固化的有机聚硅氧烷组合物 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200604291A (en) * | 2004-07-09 | 2006-02-01 | Dow Corning Toray Co Ltd | Room-temperature curable organopolysiloxane composition and electrical or electronic devices |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3725178B2 (ja) * | 1991-03-22 | 2005-12-07 | 東レ・ダウコーニング株式会社 | 室温硬化性オルガノポリシロキサン組成物 |
| US7307134B2 (en) * | 2002-02-22 | 2007-12-11 | Henkel Corporation | Mixed alkoxysilyl functional polymers |
| JP4860099B2 (ja) * | 2003-03-12 | 2012-01-25 | 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 | 室温硬化性ポリオルガノシロキサン組成物 |
| JP2004269817A (ja) * | 2003-03-12 | 2004-09-30 | Ge Toshiba Silicones Co Ltd | 室温硬化性ポリオルガノシロキサン組成物の製造方法 |
| JP4283009B2 (ja) * | 2003-03-12 | 2009-06-24 | 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 | 室温硬化性ポリオルガノシロキサン組成物 |
| JP4180477B2 (ja) * | 2003-09-10 | 2008-11-12 | 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 | 室温硬化性ポリオルガノシロキサン組成物 |
| JP4799835B2 (ja) * | 2004-07-09 | 2011-10-26 | 東レ・ダウコーニング株式会社 | 室温硬化性オルガノポリシロキサン組成物、および電気・電子機器 |
-
2007
- 2007-10-25 JP JP2007278105A patent/JP5285892B2/ja active Active
-
2008
- 2008-10-02 TW TW097137994A patent/TWI462970B/zh active
- 2008-10-06 KR KR1020107008988A patent/KR101528789B1/ko active Active
- 2008-10-06 EP EP08843158A patent/EP2207856B1/en active Active
- 2008-10-06 AT AT08843158T patent/ATE548432T1/de active
- 2008-10-06 CN CN2008801117566A patent/CN101827905B/zh active Active
- 2008-10-06 WO PCT/JP2008/068517 patent/WO2009054279A1/en not_active Ceased
- 2008-10-06 US US12/739,343 patent/US8247516B2/en active Active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200604291A (en) * | 2004-07-09 | 2006-02-01 | Dow Corning Toray Co Ltd | Room-temperature curable organopolysiloxane composition and electrical or electronic devices |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2207856B1 (en) | 2012-03-07 |
| US8247516B2 (en) | 2012-08-21 |
| JP2009102591A (ja) | 2009-05-14 |
| JP5285892B2 (ja) | 2013-09-11 |
| KR20100087129A (ko) | 2010-08-03 |
| KR101528789B1 (ko) | 2015-06-15 |
| EP2207856A1 (en) | 2010-07-21 |
| ATE548432T1 (de) | 2012-03-15 |
| CN101827905A (zh) | 2010-09-08 |
| WO2009054279A1 (en) | 2009-04-30 |
| TW200932833A (en) | 2009-08-01 |
| US20100236450A1 (en) | 2010-09-23 |
| CN101827905B (zh) | 2013-04-17 |
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