JPH0331745B2 - - Google Patents

Info

Publication number: JPH0331745B2
Authority: JP; Japan
Prior art keywords: sime; composition; platinum; present; group
Prior art date: 1985-03-14
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.): Expired

Application number

JP5083985A

Other languages

English (en)

Japanese (ja)

Other versions

JPS61209271A (ja

Inventor

Hiroshige Okinoshima

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Shin Etsu Chemical Co Ltd

Original Assignee

Shin Etsu Chemical Co Ltd

Priority date (The priority date 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 date listed.)

1985-03-14

Filing date

1985-03-14

Publication date

1991-05-08

1985-03-14 Application filed by Shin Etsu Chemical Co Ltd filed Critical Shin Etsu Chemical Co Ltd

1985-03-14 Priority to JP5083985A priority Critical patent/JPS61209271A/ja

1986-03-14 Priority to US06/839,562 priority patent/US4654408A/en

1986-09-17 Publication of JPS61209271A publication Critical patent/JPS61209271A/ja

1991-05-08 Publication of JPH0331745B2 publication Critical patent/JPH0331745B2/ja

Status Granted legal-status Critical Current

Links

239000000203 mixture Substances 0.000 claims description 30
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 26
229910052697 platinum Inorganic materials 0.000 claims description 13
229920001296 polysiloxane Polymers 0.000 claims description 12
239000003054 catalyst Substances 0.000 claims description 11
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 3
150000003961 organosilicon compounds Chemical class 0.000 claims description 3
125000001183 hydrocarbyl group Chemical group 0.000 claims 1
-1 methylcyclohexyl Chemical group 0.000 description 10
239000002253 acid Substances 0.000 description 6
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 5
239000004205 dimethyl polysiloxane Substances 0.000 description 4
238000000034 method Methods 0.000 description 4
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
238000004132 cross linking Methods 0.000 description 3
230000000694 effects Effects 0.000 description 3
229920001971 elastomer Polymers 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000002683 reaction inhibitor Substances 0.000 description 3
239000005060 rubber Substances 0.000 description 3
229920002554 vinyl polymer Chemical group 0.000 description 3
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
238000007259 addition reaction Methods 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
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
150000002430 hydrocarbons Chemical group 0.000 description 2
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
229920001875 Ebonite Polymers 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
125000003545 alkoxy 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
239000003963 antioxidant agent Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 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
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
238000003763 carbonization Methods 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([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
238000007323 disproportionation reaction Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
AEPJOWQGPJRHTA-UHFFFAOYSA-N ethenyl(ethenylsilyl)silane Chemical compound C=C[SiH2][SiH2]C=C AEPJOWQGPJRHTA-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
239000000499 gel Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000011256 inorganic filler Substances 0.000 description 1
229910003475 inorganic filler Inorganic materials 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
239000002904 solvent Substances 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
RSNQKPMXXVDJFG-UHFFFAOYSA-N tetrasiloxane Chemical compound [SiH3]O[SiH2]O[SiH2]O[SiH3] RSNQKPMXXVDJFG-UHFFFAOYSA-N 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
239000008096 xylene Substances 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1

Landscapes

Compositions Of Macromolecular Compounds (AREA)

JP5083985A 1985-03-14 1985-03-14 硬化性シリコ−ン組成物 Granted JPS61209271A (ja)

Priority Applications (2)

Application Number	Priority Date	Filing Date	Title
JP5083985A JPS61209271A (ja)	1985-03-14	1985-03-14	硬化性シリコ−ン組成物
US06/839,562 US4654408A (en)	1985-03-14	1986-03-14	Curable silicone composition

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP5083985A JPS61209271A (ja)	1985-03-14	1985-03-14	硬化性シリコ−ン組成物

Publications (2)

Publication Number	Publication Date
JPS61209271A JPS61209271A (ja)	1986-09-17
JPH0331745B2 true JPH0331745B2 (de)	1991-05-08

Family

ID=12869908

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP5083985A Granted JPS61209271A (ja)	1985-03-14	1985-03-14	硬化性シリコ−ン組成物

Country Status (1)

Country	Link
JP (1)	JPS61209271A (de)

1985
- 1985-03-14 JP JP5083985A patent/JPS61209271A/ja active Granted

Also Published As

Publication number	Publication date
JPS61209271A (ja)	1986-09-17

Publication	Publication Date	Title
US6127502A (en)	2000-10-03	Polyorganosiloxanes having at least one organofunctional group with multiple hydrolyzable groups
US4529752A (en)	1985-07-16	Solvent resistant vulcanizable silicone rubber composition
JPH0633348B2 (ja)	1994-05-02	光学的に透明な硬化性ポリオルガノシロキサン組成物の調製法
US3498945A (en)	1970-03-03	Linear organopolysiloxanes their preparation and their use
JPH08208840A (ja)	1996-08-13	シリコーンレジン、これを含む組成物およびその硬化方法
EP0228775A2 (de)	1987-07-15	Härtbare Silikonzusammensetzung mit veränderter Adhäsion
EP0532362A1 (de)	1993-03-17	Silikongelzusammensetzung mit ausgezeichneter Dämpfungseigenschaft
JPH0363994B2 (de)	1991-10-03
US4722987A (en)	1988-02-02	Method for the preparation of an organopolysiloxane
US5288829A (en)	1994-02-22	Curable silicone composition
JPS63205359A (ja)	1988-08-24	硬化性フツ素シリコ−ン組成物
US5166293A (en)	1992-11-24	Silicone rubber compositions and cured products thereof
US4764577A (en)	1988-08-16	Curable polymeric composition
EP0499407A1 (de)	1992-08-19	Vernetzer und Kettenverlängerer zur Vulkanisierung oder Vernetzung von Polymeren bei Raumtemperatur
JP2741436B2 (ja)	1998-04-15	表面処理アルミナ及びそれを含有する熱伝導性シリコーン組成物
JPH0413767A (ja)	1992-01-17	硬化性シリコーン組成物及び硬化物
JP2632607B2 (ja)	1997-07-23	硬化性オルガノポリシロキサン組成物
EP0455385B1 (de)	1995-11-15	Verfahren zur Härtung von Methylhydrogensiloxanen
JPH0655894B2 (ja)	1994-07-27	オルガノポリシロキサンゲル組成物
JP2632606B2 (ja)	1997-07-23	硬化性オルガノポリシロキサン組成物
KR840007019A (ko)	1984-12-04	알콕시-말단 폴리실록산의 제조방법
JPH0633352B2 (ja)	1994-05-02	硬化性シリコーン組成物
US5283308A (en)	1994-02-01	Neutralization of polyorganosiloxanes using triorganosilanes and curable compositions containing said polyorganosiloxanes
RU2165426C1 (ru)	2001-04-20	Кремнийорганические соединения, содержащие карбамидные группы, их получение и их применение
US4654408A (en)	1987-03-31	Curable silicone composition