JP2006169411A5 - - Google Patents
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- JP2006169411A5 JP2006169411A5 JP2004365159A JP2004365159A JP2006169411A5 JP 2006169411 A5 JP2006169411 A5 JP 2006169411A5 JP 2004365159 A JP2004365159 A JP 2004365159A JP 2004365159 A JP2004365159 A JP 2004365159A JP 2006169411 A5 JP2006169411 A5 JP 2006169411A5
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- JP
- Japan
- Prior art keywords
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- parts
- silicone composition
- Prior art date
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- -1 specifically Chemical group 0.000 description 26
- 239000000203 mixture Substances 0.000 description 15
- 229920001296 polysiloxane Polymers 0.000 description 15
- 125000000217 alkyl group Chemical group 0.000 description 10
- 239000004205 dimethyl polysiloxane Substances 0.000 description 10
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 10
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 10
- 125000003342 alkenyl group Chemical group 0.000 description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 7
- 125000001183 hydrocarbyl group Chemical group 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 125000006165 cyclic alkyl group Chemical group 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 125000006038 hexenyl group Chemical group 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 2
- 125000006022 2-methyl-2-propenyl group Chemical group 0.000 description 2
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000000732 arylene group Chemical group 0.000 description 2
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000006482 condensation reaction Methods 0.000 description 2
- 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 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 125000003493 decenyl group Chemical group [H]C([*])=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])[H] 0.000 description 2
- 239000012975 dibutyltin dilaurate Substances 0.000 description 2
- 125000005066 dodecenyl group Chemical group C(=CCCCCCCCCCC)* 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- IIPYXGDZVMZOAP-UHFFFAOYSA-N lithium nitrate Chemical compound [Li+].[O-][N+]([O-])=O IIPYXGDZVMZOAP-UHFFFAOYSA-N 0.000 description 2
- 125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920002379 silicone rubber Polymers 0.000 description 2
- 239000004945 silicone rubber Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000005063 tetradecenyl group Chemical group C(=CCCCCCCCCCCCC)* 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 2
- 125000005040 tridecenyl group Chemical group C(=CCCCCCCCCCCC)* 0.000 description 2
- 125000005065 undecenyl group Chemical group C(=CCCCCCCCCC)* 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- AGKBXKFWMQLFGZ-UHFFFAOYSA-N (4-methylbenzoyl) 4-methylbenzenecarboperoxoate Chemical compound C1=CC(C)=CC=C1C(=O)OOC(=O)C1=CC=C(C)C=C1 AGKBXKFWMQLFGZ-UHFFFAOYSA-N 0.000 description 1
- QMTFKWDCWOTPGJ-KVVVOXFISA-N (z)-octadec-9-enoic acid;tin Chemical compound [Sn].CCCCCCCC\C=C/CCCCCCCC(O)=O QMTFKWDCWOTPGJ-KVVVOXFISA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 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
- BJISXPRYXCKVSD-UHFFFAOYSA-J 3-oxobutanoate;titanium(4+) Chemical compound [Ti+4].CC(=O)CC([O-])=O.CC(=O)CC([O-])=O.CC(=O)CC([O-])=O.CC(=O)CC([O-])=O BJISXPRYXCKVSD-UHFFFAOYSA-J 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- 229920001174 Diethylhydroxylamine Polymers 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- GSCOPSVHEGTJRH-UHFFFAOYSA-J [Ti+4].CCCC(=O)CC([O-])=O.CCCC(=O)CC([O-])=O.CCCC(=O)CC([O-])=O.CCCC(=O)CC([O-])=O Chemical compound [Ti+4].CCCC(=O)CC([O-])=O.CCCC(=O)CC([O-])=O.CCCC(=O)CC([O-])=O.CCCC(=O)CC([O-])=O GSCOPSVHEGTJRH-UHFFFAOYSA-J 0.000 description 1
- QSEFDHMKKQTTHD-UHFFFAOYSA-N [Zr+4].I Chemical class [Zr+4].I QSEFDHMKKQTTHD-UHFFFAOYSA-N 0.000 description 1
- NBJODVYWAQLZOC-UHFFFAOYSA-L [dibutyl(octanoyloxy)stannyl] octanoate Chemical compound CCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCC NBJODVYWAQLZOC-UHFFFAOYSA-L 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000002344 aminooxy group Chemical group [H]N([H])O[*] 0.000 description 1
- 239000002585 base Substances 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
- WBQJELWEUDLTHA-UHFFFAOYSA-M benzyl(triethyl)azanium;acetate Chemical compound CC([O-])=O.CC[N+](CC)(CC)CC1=CC=CC=C1 WBQJELWEUDLTHA-UHFFFAOYSA-M 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- LUZSPGQEISANPO-UHFFFAOYSA-N butyltin Chemical compound CCCC[Sn] LUZSPGQEISANPO-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- FVCOIAYSJZGECG-UHFFFAOYSA-N diethylhydroxylamine Chemical compound CCN(O)CC FVCOIAYSJZGECG-UHFFFAOYSA-N 0.000 description 1
- VEVVRTWXUIWDAW-UHFFFAOYSA-N dodecan-1-amine;phosphoric acid Chemical compound OP(O)(O)=O.CCCCCCCCCCCCN VEVVRTWXUIWDAW-UHFFFAOYSA-N 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 229940093858 ethyl acetoacetate Drugs 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- VMESOKCXSYNAKD-UHFFFAOYSA-N n,n-dimethylhydroxylamine Chemical compound CN(C)O VMESOKCXSYNAKD-UHFFFAOYSA-N 0.000 description 1
- 125000002801 octanoyl group Chemical group C(CCCCCCC)(=O)* 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- LSZKGNJKKQYFLR-UHFFFAOYSA-J tri(butanoyloxy)stannyl butanoate Chemical compound [Sn+4].CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O LSZKGNJKKQYFLR-UHFFFAOYSA-J 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004365159A JP4590253B2 (ja) | 2004-12-16 | 2004-12-16 | オルガノポリシロキサンおよびシリコーン組成物 |
| TW094142314A TW200634056A (en) | 2004-12-16 | 2005-12-01 | Organopolysiloxane and silicone composition |
| EP05816452A EP1824903B1 (en) | 2004-12-16 | 2005-12-12 | Organopolysiloxane and silicone composition |
| KR1020077013459A KR20070089161A (ko) | 2004-12-16 | 2005-12-12 | 오가노폴리실옥산 및 실리콘 조성물 |
| DE602005014268T DE602005014268D1 (de) | 2004-12-16 | 2005-12-12 | Organopolysiloxan und silikonzusammensetzung |
| AT05816452T ATE430175T1 (de) | 2004-12-16 | 2005-12-12 | Organopolysiloxan und silikonzusammensetzung |
| CN2005800460517A CN101098912B (zh) | 2004-12-16 | 2005-12-12 | 有机基聚硅氧烷和有机硅组合物 |
| PCT/JP2005/023195 WO2006064928A1 (en) | 2004-12-16 | 2005-12-12 | Organopolysiloxane and silicone composition |
| US11/721,788 US7622539B2 (en) | 2004-12-16 | 2005-12-12 | Organopolysiloxane and silicone composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004365159A JP4590253B2 (ja) | 2004-12-16 | 2004-12-16 | オルガノポリシロキサンおよびシリコーン組成物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006169411A JP2006169411A (ja) | 2006-06-29 |
| JP2006169411A5 true JP2006169411A5 (https=) | 2008-01-17 |
| JP4590253B2 JP4590253B2 (ja) | 2010-12-01 |
Family
ID=35695827
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004365159A Expired - Fee Related JP4590253B2 (ja) | 2004-12-16 | 2004-12-16 | オルガノポリシロキサンおよびシリコーン組成物 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7622539B2 (https=) |
| EP (1) | EP1824903B1 (https=) |
| JP (1) | JP4590253B2 (https=) |
| KR (1) | KR20070089161A (https=) |
| CN (1) | CN101098912B (https=) |
| AT (1) | ATE430175T1 (https=) |
| DE (1) | DE602005014268D1 (https=) |
| TW (1) | TW200634056A (https=) |
| WO (1) | WO2006064928A1 (https=) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8907026B2 (en) | 2004-12-23 | 2014-12-09 | Dow Corning Corporation | Crosslinkable saccharide-siloxane compositions, and networks, coatings and articles formed therefrom |
| JP5122444B2 (ja) | 2005-05-23 | 2013-01-16 | ダウ・コーニング・コーポレイション | サッカリド−シロキサンコポリマーを含むパーソナルケア組成物 |
| CN101478973B (zh) | 2006-05-23 | 2013-08-28 | 陶氏康宁公司 | 用于递送活性成分的新型硅氧烷成膜剂 |
| US20080135721A1 (en) * | 2006-12-06 | 2008-06-12 | General Electric Company | Casting compositions for manufacturing metal casting and methods of manufacturing thereof |
| JP5207627B2 (ja) * | 2006-12-27 | 2013-06-12 | 東レ・ダウコーニング株式会社 | オルガノポリシロキサンの熱安定性を改善する方法およびオルガノポリシロキサン混合物 |
| WO2008103219A1 (en) | 2007-02-20 | 2008-08-28 | Dow Corning Coration | Filler treating agents based on hydrogen bonding polyorganosiloxanes |
| JP5053714B2 (ja) * | 2007-05-30 | 2012-10-17 | 株式会社カネカ | 付加型硬化性シリコーン組成物 |
| JP5372388B2 (ja) * | 2008-01-30 | 2013-12-18 | 東レ・ダウコーニング株式会社 | 熱伝導性シリコーングリース組成物 |
| JP5469874B2 (ja) * | 2008-09-05 | 2014-04-16 | 東レ・ダウコーニング株式会社 | 硬化性オルガノポリシロキサン組成物、光半導体素子封止剤および光半導体装置 |
| JP2010100784A (ja) * | 2008-10-27 | 2010-05-06 | Asahi Kasei Corp | 表面改質された無機化合物微粒子及びその分散体 |
| US8618211B2 (en) | 2009-03-16 | 2013-12-31 | Dow Corning Corporation | Thermally conductive grease and methods and devices in which said grease is used |
| JP5584989B2 (ja) * | 2009-03-31 | 2014-09-10 | Ｄｉｃ株式会社 | 表面修飾シリカ粒子及びそれを用いた活性エネルギー線硬化型樹脂組成物 |
| JP2011140566A (ja) * | 2010-01-07 | 2011-07-21 | Dow Corning Toray Co Ltd | 熱伝導性シリコーングリース組成物 |
| JP5365572B2 (ja) | 2010-04-13 | 2013-12-11 | 信越化学工業株式会社 | 室温湿気増粘型熱伝導性シリコーングリース組成物 |
| WO2012027073A1 (en) | 2010-08-23 | 2012-03-01 | Dow Corning Corporation | Saccharide siloxanes stable in aqueous environments and methods for the preparation and use of such saccharide siloxanes |
| CN102382631A (zh) * | 2010-08-30 | 2012-03-21 | 天津莱尔德电子材料有限公司 | 粘度可控高性能硅基导热膏及其制备方法 |
| JP5614217B2 (ja) * | 2010-10-07 | 2014-10-29 | デクセリアルズ株式会社 | マルチチップ実装用緩衝フィルム |
| CN101982502B (zh) * | 2010-10-22 | 2012-05-09 | 北京化工大学 | 一种弹性体热界面材料及其制备方法 |
| JP5553006B2 (ja) * | 2010-11-12 | 2014-07-16 | 信越化学工業株式会社 | 熱伝導性シリコーングリース組成物 |
| JP5585529B2 (ja) * | 2011-05-06 | 2014-09-10 | 信越化学工業株式会社 | 末端アルコキシ変性オルガノポリシロキサン及びその製造方法 |
| JP5644747B2 (ja) * | 2011-12-13 | 2014-12-24 | 信越化学工業株式会社 | 熱伝導性シリコーン組成物及びその硬化物 |
| BR112014026360A2 (pt) | 2012-04-23 | 2017-06-27 | Gen Electric | aerofólio de turbina e pá de turbina |
| JP2015537062A (ja) * | 2012-09-28 | 2015-12-24 | ダンマークス・テクニスケ・ウニヴェルジテートＤａｎｍａｒｋｓ Ｔｅｋｎｉｓｋｅ Ｕｎｉｖｅｒｓｉｔｅｔ | 機械的に見分けのつかないポリマーコーティング |
| KR20190020776A (ko) * | 2016-06-24 | 2019-03-04 | 다우 코닝 도레이 캄파니 리미티드 | 화장료용 분체의 처리제, 화장료용 분체 및 이를 배합한 화장료 |
| US10344194B2 (en) | 2017-09-27 | 2019-07-09 | Momentive Performance Materials Inc. | Thermal interface composition comprising ionically modified siloxane |
| CN107987536A (zh) * | 2018-01-04 | 2018-05-04 | 楼旭娟 | 一种高导热绝缘硅胶片及其制作方法 |
| WO2019150944A1 (ja) * | 2018-01-31 | 2019-08-08 | 積水ポリマテック株式会社 | 熱伝導性組成物及び熱伝導性成形体 |
| TWI861243B (zh) * | 2019-10-30 | 2024-11-11 | 日商陶氏東麗股份有限公司 | 有機聚矽氧烷、其製造方法以及導熱性矽組成物 |
| CN115362217B (zh) * | 2020-04-06 | 2024-09-13 | 积水化学工业株式会社 | 树脂组合物、散热构件及电子设备 |
| US12503554B2 (en) * | 2020-05-07 | 2025-12-23 | Dow Silicones Corporation | (Meth)acrylate functional silicone and methods for its preparation and use |
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| CN119731271A (zh) * | 2022-10-28 | 2025-03-28 | 捷恩智株式会社 | 硅酮树脂组合物 |
| CN116355218A (zh) * | 2023-03-29 | 2023-06-30 | 浙江新安化工集团股份有限公司 | 一种异端乙烯基羟基聚硅氧烷及其制备方法和用途 |
| WO2025187757A1 (ja) * | 2024-03-07 | 2025-09-12 | 積水化学工業株式会社 | 樹脂組成物、放熱部材、及び電子機器 |
| WO2026042504A1 (ja) * | 2024-08-23 | 2026-02-26 | 信越化学工業株式会社 | 有機ケイ素化合物及びその製造方法並びに添加剤 |
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| JPS58162660A (ja) | 1982-03-19 | 1983-09-27 | Toray Silicone Co Ltd | プライマ−組成物 |
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| US5300608A (en) * | 1992-03-31 | 1994-04-05 | Loctite Corporation | Process for preparing alkoxy-terminated organosiloxane fluids using organo-lithium reagents |
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| JPH0912724A (ja) | 1995-06-30 | 1997-01-14 | Toray Dow Corning Silicone Co Ltd | ジオルガノポリシロキサンの製造方法 |
| JP2000038508A (ja) * | 1998-07-23 | 2000-02-08 | Ge Toshiba Silicones Co Ltd | 熱伝導性の室温硬化性ポリオルガノシロキサン組成物 |
| JP3543663B2 (ja) | 1999-03-11 | 2004-07-14 | 信越化学工業株式会社 | 熱伝導性シリコーンゴム組成物及びその製造方法 |
| JP4727017B2 (ja) | 1999-11-15 | 2011-07-20 | 東レ・ダウコーニング株式会社 | 熱伝導性シリコーンゴム組成物 |
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-
2004
- 2004-12-16 JP JP2004365159A patent/JP4590253B2/ja not_active Expired - Fee Related
-
2005
- 2005-12-01 TW TW094142314A patent/TW200634056A/zh unknown
- 2005-12-12 AT AT05816452T patent/ATE430175T1/de not_active IP Right Cessation
- 2005-12-12 DE DE602005014268T patent/DE602005014268D1/de not_active Expired - Lifetime
- 2005-12-12 KR KR1020077013459A patent/KR20070089161A/ko not_active Abandoned
- 2005-12-12 WO PCT/JP2005/023195 patent/WO2006064928A1/en not_active Ceased
- 2005-12-12 US US11/721,788 patent/US7622539B2/en not_active Expired - Fee Related
- 2005-12-12 CN CN2005800460517A patent/CN101098912B/zh not_active Expired - Fee Related
- 2005-12-12 EP EP05816452A patent/EP1824903B1/en not_active Expired - Lifetime
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