KR840007737A - 다성분 무용매 실리콘 탈형 피복 조성물 - Google Patents
다성분 무용매 실리콘 탈형 피복 조성물 Download PDFInfo
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- KR840007737A KR840007737A KR1019840000176A KR840000176A KR840007737A KR 840007737 A KR840007737 A KR 840007737A KR 1019840000176 A KR1019840000176 A KR 1019840000176A KR 840000176 A KR840000176 A KR 840000176A KR 840007737 A KR840007737 A KR 840007737A
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- 229920001296 polysiloxane Polymers 0.000 title claims 10
- 239000008199 coating composition Substances 0.000 title claims 2
- 238000000034 method Methods 0.000 claims 16
- 239000000203 mixture Substances 0.000 claims 10
- 125000004432 carbon atom Chemical group C* 0.000 claims 9
- -1 polysiloxane Polymers 0.000 claims 8
- 150000001733 carboxylic acid esters Chemical class 0.000 claims 6
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 5
- 239000004215 Carbon black (E152) Substances 0.000 claims 5
- 150000001336 alkenes Chemical class 0.000 claims 5
- 229930195733 hydrocarbon Natural products 0.000 claims 5
- 229910000510 noble metal Inorganic materials 0.000 claims 4
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims 4
- 229920005601 base polymer Polymers 0.000 claims 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 3
- 239000003054 catalyst Substances 0.000 claims 3
- 150000002148 esters Chemical class 0.000 claims 3
- 239000012530 fluid Substances 0.000 claims 3
- 239000003112 inhibitor Substances 0.000 claims 3
- 229910052751 metal Inorganic materials 0.000 claims 3
- 239000002184 metal Substances 0.000 claims 3
- 239000010948 rhodium Substances 0.000 claims 3
- 229910052703 rhodium Inorganic materials 0.000 claims 3
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 3
- 229920002554 vinyl polymer Polymers 0.000 claims 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 claims 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 claims 2
- 239000011248 coating agent Substances 0.000 claims 2
- 238000000576 coating method Methods 0.000 claims 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 229920006136 organohydrogenpolysiloxane Polymers 0.000 claims 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 2
- SXUXGFHXUDLTFO-UHFFFAOYSA-N (Z)-4-oxo-4-silyloxybut-2-enoic acid Chemical compound OC(=O)C=C/C(=O)O[SiH3] SXUXGFHXUDLTFO-UHFFFAOYSA-N 0.000 claims 1
- 239000004971 Cross linker Substances 0.000 claims 1
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 claims 1
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 150000001721 carbon Chemical class 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 150000004696 coordination complex Chemical class 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 239000003431 cross linking reagent Substances 0.000 claims 1
- 229910021419 crystalline silicon Inorganic materials 0.000 claims 1
- LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 claims 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 238000006459 hydrosilylation reaction Methods 0.000 claims 1
- 150000002632 lipids Chemical class 0.000 claims 1
- 239000011976 maleic acid Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 229910052697 platinum Inorganic materials 0.000 claims 1
- 230000001737 promoting effect Effects 0.000 claims 1
- 229910000077 silane Inorganic materials 0.000 claims 1
- 125000005372 silanol group Chemical group 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 230000009885 systemic effect Effects 0.000 claims 1
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- 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
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- 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
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- 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
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- 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
- C08G77/16—Polysiloxanes containing silicon bound to oxygen-containing groups to hydroxyl groups
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- 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
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- 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
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/24—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen halogen-containing groups
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- 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
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
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Abstract
내용 없음.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (21)
- (a) 100중량부의 성분 A를 5내지 100부의 성분 B 및 3내지 10부의 성분 C와 혼합시키고, (여기서, 성분 A는 올레핀 오가노폴리실록산 또는 실란올말단 오가노폴리실록산 기본중합체이고. 성분 B는 비닐실리콘 유체에 분산시킨 귀금속 또는 귀금속 착화물 촉매이며, 성분 C는 오가노하이드로겐 폴리실록산 가교 결합제이다) ; (b) 성분 A, 성분 B 및 성분 C로 이루어진 혼합물을 적당한 지질상에 피복시키고 ; (c) 언급된 기질상의 피복을 경화시키는 단계로 이루어짐을 특징으로 하여 실리콘 탈형 피복조성물이 경화된 기질을 제조하는 방법.
- 제1항에 있어서, 언급된 기본 중합체가 하기 일반식(I)의 구조적 유니트를 갖는 올레핀 오가노폴리실록산(25℃에서의 점도 약 10 내지 약 5,000 센티포이즈)이거나, 하기 일반식(Ia)의 실란을 말단오가노폴리실록산(25℃에서의 점도 : 약 10 내지 5,000 센티포이즈)인 제조 방법 :상기식에서, R은 C-Si 결합에 의하여 실리콘 원자에 결합되는 탄소수 1내지 30의 유기 라디칼로서, 1가의 탄화수소라디칼, 할로겔화 1가의 탄화수소라디칼, 및 시아노알킬 라디칼 및 이들의 혼합물로부터 선택되며, R1은 1내지 20개의 탄소원자를 갖는 올레핀계 탄화수소 라디칼이며, a는 0내지 3이고, b는 약 0.005 내지 약2.0(단, a와 b의 합은 0.8 내지 3이다)이며, X는 실란올 말단 오가노폴리실록산의 25℃에서의 점도가 약 10내지 5,000 센티포이즈가 될 수 있는 값이다.
- 제1항에 있어서, 언급된 오가노하아드로겐 폴리실록산 가교결합제가 하기 일반식(II)의 구조적 유니트를 가지며, 25℃에서의 점도가 약 10내지 5,000 센티포이즈인 제조방법 ;상기식에서, R은 1가의 탄화수소라디칼, 할로겐화 1가의 탄화수소 라디칼, 및 시아노 알킬라디칼 및 이들의 혼합물로 부터 선택되는 탄소수 1내지 30의 유기라디칼이며, a는 0내지 3이고, b는 약 0.005 내지 약 2.0(단, a와 b의 합은 0.8 내지 3이다)이다.
- 제2항에 있어서, R이 메틸인 제조방법.
- 제3항에 있어서, R이 메틸인 제조방법.
- 제2항에 있어서, R1이 비닐 또는 알릴인 제조방법.
- 제1항에 있어서, 언급된 올레핀 오가노폴리실록산이 최고 2.5중량%까지의 비닐을 함유하는 디메틸비닐 말단디메틸메틸비닐폴리실록산 공중합체 유체(25℃에서의 점도 100 내지 1,000 센티포이즈)인 제조방법
- 제1항에 있어서, 언급된 오가노하이드로겐 폴리실록산이 약 0.1 내지 1.67중량%의 수소를 함유하는 트리메틸 말단 메틸하이드로겐 폴리실록산 유체(25℃에서의 점도 : 약 10 내지 500 센티포이즈)인 제조방법.
- 제1항에 있어서, 언급된 귀금속 촉매가 플라티늄금속, 로듐금속, 플라티늄금속의 착화물 및 로듐금속의 착화물인 제조방법.
- 제9항에 있어서, 언급된 귀금속촉매가 기본중합체 1,000,000부당 약 5내지 500부의 플라티늄 또는 로듐금속이 제공되기에 충분한 양으로 존재하는 제조방법.
- 제1항에 있어서, 성분 A, 성분 B 및 성분 C의 혼합물 100부에 0.1 내지 5부의 성분 D(여기서, 성분 D는 주위온도에서 하이드로실레이션 경화반응의 억제에는 효과적이지만, 상승된 온도에서의 언급된 반응은 억제하지 않는 억제제이다)를 혼합시키는 단계를 추가로 포함하는 제조방법.
- 제11항에 있어서, 언급된 억제제가 불포화탄소를 함유하는 디알킬카복실에스테르, 아세틸렌 그룹을 함유하는 화합물, 지방족, 알콜의 올레핀계 카복실산 에스테르(여기서, 지방족알콜은 1내지 4개의 탄소원자를 가지며, 올레핀계 카복실산은 2내지 10개의 탄소 원자를 갖는다), 알케닐 이소시아누레이트(여기서, 알케닐 그룹은 3내지 8개의 탄소원자를 갖는다), 디알킬아세틸렌디카복실레이트 및 불포화탄소를 함유하는 디알킬 카복실에스테르와 지방족 알콜의 올레핀계 카복실산 에스테르의 혼합물(여기서, 지방족 알콜은 1내지 4개의 탄소 원자를 가지며, 올레핀계 카복실산은 2내지 10개의 탄소 원자를 갖는다.)로 부터 선택되는 제조방법.
- 제11항에 있어서, 언급된 억제제가 불포화 탄소를 함유하는 디알킬 카복실 에스테르와 지방족 알콜의 올레핀계 카복실산 에스테르(여기서, 지방족 알콜은 1내지 4개의 탄소원자를 가지며, 올레핀계 카복실산은 2내지 10개의 탄소자원를 갖는다)의 혼합물인 제조방법.
- 제13항에 있어서, 언급된 디알킬카복실 에스테르가 디알릴말레에이트 ; 부틸알릴말레에이트, 디알릴석 시네이트 ; 및 디메틸말레에이트, 디에틸 말레에이트 및 실일말레에이트로 부터 선택된 말레산의 디알킬에스테르로부터 선택되는 제조방법.
- 제13항에 있어서, 언급된 지방족 알콜의 올레핀계 카복실산 에스테르가 비닐 아세테이트인 제조방법.
- 제13항에 있어서, 언급된 디알킬 카복실 에스테르와 지방족 알콜의 올레핀계 카복실산 에스테르를 약 1 : 24내지 약 1 : 1로 혼합시키는 제조방법.
- 제13항에 있어서, 언급된 디알킬 카복실 에스테르와 지방족 알콜의 올레핀계 카복실산 에스테르를 약 1 : 3의 비율로 혼합시키는 제조방법.
- 제13항에 있어서, 언급된 디알릴말레에이트와 비닐 아세테이트를 약 1 : 3의 비율로 혼합시키는 방법.
- 제11항에 있어서, 혼합물에 약 0.05 내지 2중량%량으로 존재하기에 충분한 억제제가 성분 D에 존재하는 제조방법.
- 제1항에 있어서, 성분 A, 성분 B 및 성분 C의 혼합물 100부에 0.1 내지 10부의 성분 E(여기서 성분 E는 언급된 부가 경화성 탈형피복조성물의 경화촉진에 효과적인 비닐 고무 경화촉진제이며, 고무의 평균분자량은 약 200,000 내지 400,000이다)를 혼합시키는 단계를 추가로 포함하는 제조방법.
- 제20항에 있어서, 언급된 고무가 부가 경화성 탈형피복조성물의 0.5중량% 이상의 량으로 혼합물에, 존재하는 제조방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US458,421 | 1983-01-17 | ||
| US06/458,421 US4448815A (en) | 1983-01-17 | 1983-01-17 | Multi-component solventless silicone release coating system |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR840007737A true KR840007737A (ko) | 1984-12-10 |
Family
ID=23820719
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019840000176A KR840007737A (ko) | 1983-01-17 | 1984-01-17 | 다성분 무용매 실리콘 탈형 피복 조성물 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US4448815A (ko) |
| EP (1) | EP0116290B1 (ko) |
| JP (1) | JPS59149961A (ko) |
| KR (1) | KR840007737A (ko) |
| AT (1) | ATE33667T1 (ko) |
| AU (1) | AU2353584A (ko) |
| DE (1) | DE3470550D1 (ko) |
| FI (1) | FI840154A (ko) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58163652A (ja) * | 1982-03-25 | 1983-09-28 | トーレ・シリコーン株式会社 | 連続的な異相構造を有するシリコ−ン１体成形物，およびその製造方法 |
| EP0112396B1 (en) * | 1982-06-15 | 1988-02-24 | Toray Silicone Co., Ltd. | Composition for forming releasable film |
| US4476166A (en) * | 1983-01-17 | 1984-10-09 | General Electric Company | Silicone release coatings and inhibitors |
| DE3315060A1 (de) * | 1983-04-26 | 1984-10-31 | Wacker-Chemie GmbH, 8000 München | Verfahren zum vernetzen von organopolysiloxanmassen |
| US4528314A (en) * | 1983-07-07 | 1985-07-09 | General Electric Company | Transparent membrane structures |
| FR2571732B1 (fr) * | 1984-10-15 | 1987-01-09 | Rhone Poulenc Spec Chim | Composition organopolysiloxanique de revetement utilisable notamment pour le traitement antiadherent et son procede d'application |
| US4562096A (en) * | 1984-12-24 | 1985-12-31 | Dow Corning Corporation | Heat-curable silicone compositions, use thereof and stabilizer therefor |
| JPS61159480A (ja) * | 1984-12-29 | 1986-07-19 | Shin Etsu Chem Co Ltd | 剥離紙用シリコ−ン組成物 |
| US4954364A (en) * | 1989-06-22 | 1990-09-04 | General Electric Company | Method for coating substrates with UV curable epoxysilicone compositions |
| US5125998A (en) * | 1989-11-03 | 1992-06-30 | Dow Corning Corporation | Process for improving the bath life and cure time of heat-curable silicone compositions |
| CA2035964A1 (en) * | 1990-03-06 | 1991-09-07 | Carl R. Kessel | Solventless silicon release coating |
| US5279860A (en) * | 1992-07-30 | 1994-01-18 | General Electric Company | Method of using epoxysilicone controlled release composition |
| US5292787A (en) * | 1992-07-30 | 1994-03-08 | General Electric Company | Epoxysilicone controlled release composition |
| US5464801A (en) * | 1993-12-30 | 1995-11-07 | Dow Corning Corporation | Catalyst compositions comprising rhodium catalyst complexes |
| US5516558A (en) * | 1994-08-24 | 1996-05-14 | General Electric Company | Addition curable paper release composition with improved bathlife |
| KR19990008020A (ko) * | 1995-04-28 | 1999-01-25 | 테릴켄트퀄리 | 광전도체를 위한 박리 층 |
| US5616672A (en) * | 1995-11-17 | 1997-04-01 | General Electric Company | Paper release compositions having improved release characteristics |
| US5766714A (en) * | 1996-01-30 | 1998-06-16 | Gold Eagle Co. | Oil resistant label system |
| US5932060A (en) * | 1997-09-12 | 1999-08-03 | General Electric Company | Paper release laminates having improved release characteristics |
| US6077611A (en) * | 1997-09-30 | 2000-06-20 | General Electric Company | Printable paper release compositions |
| US6428897B1 (en) | 1999-09-24 | 2002-08-06 | General Electric Company | Low temperature curable organopolysiloxane coatings |
| US7090923B2 (en) | 2003-02-12 | 2006-08-15 | General Electric Corporation | Paper release compositions having improved adhesion to paper and polymeric films |
| US20050282977A1 (en) * | 2004-06-17 | 2005-12-22 | Emil Stempel | Cross-linked gel and pressure sensitive adhesive blend, and skin-attachable products using the same |
| JP4684835B2 (ja) * | 2005-09-30 | 2011-05-18 | 信越化学工業株式会社 | シリコーンゴム硬化物の表面タック性を低減する方法、半導体封止用液状シリコーンゴム組成物、シリコーンゴム封止型半導体装置、及び該半導体装置の製造方法 |
| US20090247680A1 (en) * | 2006-06-06 | 2009-10-01 | Avery Dennison Corporation | Adhesion promoting additive |
| DE102008027502A1 (de) * | 2008-06-10 | 2009-12-17 | Tesa Se | Verfahren zur Herstellung von Releaselinern |
| JP5559688B2 (ja) * | 2008-07-22 | 2014-07-23 | 電気化学工業株式会社 | 樹脂組成物 |
| MX2013003600A (es) | 2010-10-05 | 2013-07-29 | Eco Friendly Solutions Llc | Revestimiento de liberacion. |
| CN110577661B (zh) * | 2019-09-26 | 2022-02-01 | 江苏中迪新材料技术有限公司 | 一种硅胶膜、导热硅胶片及其制备方法 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1304362A (ko) * | 1969-04-25 | 1973-01-24 | ||
| US3925277A (en) * | 1972-12-20 | 1975-12-09 | Gen Electric | Process for packaging and mixing a two-part room temperature vulcanizable silicone rubber composition |
| US4071644A (en) * | 1974-11-14 | 1978-01-31 | General Electric Company Silicone Products Department | Method for rendering flexible sheet material non-adherent |
| DE2638452B2 (de) * | 1976-08-26 | 1980-02-14 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Formkorpern aus Organopolysiloxanolen |
| US4256870A (en) * | 1979-05-17 | 1981-03-17 | General Electric Company | Solventless release compositions, methods and articles of manufacture |
| US4262107A (en) * | 1979-10-04 | 1981-04-14 | General Electric Company | Rhodium catalyzed silicone rubber compositions |
| US4322320A (en) * | 1980-04-28 | 1982-03-30 | General Electric Company | Process for formulating silicone rubber products |
| US4347346A (en) * | 1981-04-02 | 1982-08-31 | General Electric Company | Silicone release coatings and inhibitors |
| US4340647A (en) * | 1981-05-22 | 1982-07-20 | General Electric Company | Vinyl gum cure accelerators for addition-cure silicone |
| DE3131734A1 (de) * | 1981-08-11 | 1983-02-24 | Bayer Ag, 5090 Leverkusen | Hitzehaertbare organopolysiloxan-mischungen |
-
1983
- 1983-01-17 US US06/458,421 patent/US4448815A/en not_active Ceased
-
1984
- 1984-01-12 EP EP19840100263 patent/EP0116290B1/en not_active Expired
- 1984-01-12 DE DE8484100263T patent/DE3470550D1/de not_active Expired
- 1984-01-12 AT AT84100263T patent/ATE33667T1/de not_active IP Right Cessation
- 1984-01-16 FI FI840154A patent/FI840154A/fi not_active Application Discontinuation
- 1984-01-17 AU AU23535/84A patent/AU2353584A/en not_active Abandoned
- 1984-01-17 JP JP59006231A patent/JPS59149961A/ja active Granted
- 1984-01-17 KR KR1019840000176A patent/KR840007737A/ko not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU2353584A (en) | 1984-07-19 |
| FI840154A0 (fi) | 1984-01-16 |
| JPH0136871B2 (ko) | 1989-08-02 |
| DE3470550D1 (en) | 1988-05-26 |
| EP0116290B1 (en) | 1988-04-20 |
| US4448815A (en) | 1984-05-15 |
| FI840154A (fi) | 1984-07-18 |
| ATE33667T1 (de) | 1988-05-15 |
| EP0116290A1 (en) | 1984-08-22 |
| JPS59149961A (ja) | 1984-08-28 |
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| Date | Code | Title | Description |
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| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |