KR910020148A - 실릴 치환 구아니딘 촉진제를 포함하는 폴리우레탄 밀봉 접착제 조성물 - Google Patents
실릴 치환 구아니딘 촉진제를 포함하는 폴리우레탄 밀봉 접착제 조성물 Download PDFInfo
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Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (11)
- (a) 하기 일반식의 실란 말단기 폴리우레탄 중합체와,(상기식에서, R는 C1-C6의 저급 알킬기이며, R1는 이가 탄화수소 라디칼, 이가 탄화수소 에테르 라디칼 및 이가 탄화수소 아미노 라디칼등으로부터 선택되는 이가 다리걸친 라디칼이며, A는 R2가 수소 또는 C1-C6의 저급 알킬일 때 -S- 및 -NH2-로부터 선택되는 라디칼이다.) (b)상기 폴리우레탄 중합체 100중량부에 대하여, 하기 일반식을 갖는 아미노실란 0.2 내지 1.0 중량부와,(상기 식에서, X는 1-3의 정수이며, R3및 R4동일하거나, 상이하고, C1-C4의 알킬로부터 선택되며, R5는 C1-C4의 알킬기 또는 C1-C4의 알콕시기이며, R6는 y 및 z가 동일하거나 상이한 1-3의 정수일 때 R7이 수소원자 또는 -(CH2)zNH2일 때 수소원자 또는 -(CH2)yNHR7이다.)c)상기 우레탄 중합체 100중량부에 대하여 하기 일반식을 갖는 화합물 또는 이들의 혼합물로부터 선택되는 촉진제0.2 내지 1.0 중량부화,(상기 식에서 , X 및 R은 상술한 바와같으며, R8은 수소원자 또는 R3, R4, R5및 X가 상술한 바와같은때이며, R9및 R10수소원자이거나 또는 부착되는 탄소원자와 함께 포화된 육원고리를 형성하며, R11, R12, E13및 R14는 각각 수소원자 또는 C1-C4의 알킬기가 된다.)로 되는 일성분계 습윤 경화성 밀봉제조성물.
- 제1항에 있어서, 상기 폴리우레탄 중합체가, 한 분자당 적어도 두 개의 히드록시기를 포함하고, 약 1000 내지 3000의 평균 분자량수를 갖는 폴리에테르 폴리올과, 분자당 적어도 두 개의 이소이아네이트기를 갖는 이소시아네이트와의 반응 생성물인 이성분계 습윤 경화성 밀봉제조성물.
- 제1항 또는 제2항에 있어서, 상기 폴리우레탄 중합체가 약 10,000 내지 30,000의 평균 분자량 수를 갖는 일성분계 습윤 경화성 밀봉제조성물.
- 제3항에 있어서,A가 R2가 상술한 바와 같을 때 ―NR2인 일성분계 습윤 경화성 밀봉제조성물.
- 상기 항들 중 어느 한 항에 있어서, 상기 폴리우레탄 중합체 100중량부에 대하여 0.4 내지 0.8 중량부의 아미노실란을 포함하는 일성분계 습윤 경화성 밀봉제조성물.
- 제5항에 있어서, 상기 아미노실란이 N-(β-아미노에틸)-γ-아미노프로필 트리메톡시실란인 일성분계 습윤 경화성 밀봉제조성물.
- 상기 항들 중 어느 한 항에 있어서, 상기 폴리우레탄 중합체 100 중량부에 대하여 0.2 내지 0.8 중량부의 촉진제를 포함하는 일성분계 습윤 경화성 밀종제조성물.
- 상기 항들 중 어느 한 항에 있어서, 상기 촉진제가 (1)N"―[2―히드록시―3―[3―(트리메톡시실릴) 프로폭시]-프로필-N,N,N`,N`, -테트라메틸구아니딘, (2) N"―[2―히드록시―3―[3―(에톡시디메틸실릴) 프로폭시]-프로필]―N,N,N`,N`, -테트라메틸구아니딘, (3) N"―[2―히드록시―3―[3―(디에톡시디메틸실릴) 프로폭시]-프로필]―N,N,N`,N`,-테트라메틸구아니딘, (4) N"―[4―[2―(트리메톡시실릴)에틸]―2―히드록시시클로헥실]―N,N,N`,N`, -테트라메틸구아니딘, (5) [3-(트리에톡시실릴) 프로필] 카바민산, [2-[[비스-(디메틸아미노)메틸렌]아미노-1-[[3-(트리메톡시실릴)프로폭시]메틸]에틸]에스테르, (6) [3-(트리에톡시실릴) 프로필] 카바민산, [2-[[비스-(디메틸아미노)메틸렌]아미노-1-[[3-(메톡시디메틸실릴)프로폭시]메틸]에틸]에스테르, (7) [3-(트리에톡시실릴) 프로필] 카바민산, [2-[[비스-(디메틸아미노)메틸렌]아미노-1-[[3-(메톡시디메틸실릴)프로폭시]메틸]에틸]에스테르, 및 (8) [3-(트리에톡시실릴) 프로필] 카바민산, [2-[[비스-(디메틸아미노)메틸렌]아미노-5-[2-(트리메톡시실릴)에틸]에스테르로부터 선택되는 일성분계 습윤 경화성 밀봉제조성물.
- 하기 일반식을 갖는 화합물들로부터 선택되는 촉진제화합물.(상기 식에서, X는 1-3의 정수이며,R은 C1-C6의 알킬기이며, R8은 수소원자 또는 X가 상술한 바와같으며, R3, R4, R5가 C1-C4의 알킬기일 때,이며, R9및 R10수소원자이거나, 또는 부착된 탄소원자와 함께 포화 육원고리를 형성하며,R11, R12, R13및 R14는 각각 수소원자 또는 C1-C4의 알킬기이다.
- 제9항에 있어서, (1)N"―[2―히드록시―3―[3―(트리메톡시실릴) 프로폭시]-프로필-N,N,N`,N`,-테트라메틸구아니딘, (2)N"―[2―히드록시―3―[3―(에톡시디메틸실릴) 프로폭시]-프로필-N,N,N`,N`,-테트라메틸구아니딘, (3)N"―[2―히드록시―3―[3―(디에톡시메틸실릴) 프로폭시]-프로필-N,N,N`,N`,-테트라메틸구아니딘, (4) N"―[4―[2―(트리메톡시실릴)에틸]―2―히드록시시클로헥실]―N,N,N`,N`,-테트라메틸구아니딘, (5) [3-(트리에톡시실릴) 프로필] 카바민산, [2-[[비스-(디메틸아미노)메틸렌]아미노-1-[[3-(트리메톡시실릴)프로필렌]아미노]-1-[[3-(트리메톡시실릴) 프로폭시]메틸]에틸]에스테르, (6) [3-(트리에톡시실릴) 프로필] 카바민산, [2-[[비스-(디메틸아미노)메틸렌]아미노-1-[[3-(에톡시디메틸실릴)프로폭시]메틸]에틸]에스테르, (7) [3-(트리에톡시실릴) 프로필] 카바민산, [2-[[비스-(디메틸아미노)메틸렌]아미노-1-[[3-(디메톡시디메틸실릴)프로폭시]메틸]에틸]에스테르, 및 (8) [3-(트리에톡시실릴) 프로필] 카바민산, [2-[[비스-(디메틸아미노)메틸렌]아미노-5-[2-(트리메톡시실릴)에틸]에스테르로부터 선택되는 촉진제화합물.
- 유리판과 금속 지지체 사이의 접합에 대하여, 제1항 내지 제8항중 어느 한 항에 따른 습윤 경화성 밀봉제조성물을 적용하는 밀봉방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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Application Number | Priority Date | Filing Date | Title |
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US07/530,752 | 1990-05-29 | ||
US07/530,752 US5097053A (en) | 1988-10-13 | 1990-05-29 | Fast-cure polyurethane sealant composition containing silyl-substituted guanidine accelerators |
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KR910020148A true KR910020148A (ko) | 1991-12-19 |
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KR1019910008803A KR910020148A (ko) | 1990-05-29 | 1991-05-29 | 실릴 치환 구아니딘 촉진제를 포함하는 폴리우레탄 밀봉 접착제 조성물 |
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US (1) | US5097053A (ko) |
EP (1) | EP0459300A3 (ko) |
KR (1) | KR910020148A (ko) |
AU (1) | AU7733091A (ko) |
BR (1) | BR9102183A (ko) |
CA (1) | CA2040215A1 (ko) |
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EP1717254A1 (de) * | 2005-04-29 | 2006-11-02 | Sika Technology AG | Feuchtigkeitshärtende Zusammensetzung mit erhöhter Dehnbarkeit |
CA2564452C (en) * | 2005-10-14 | 2014-02-18 | Chem Link, Inc. | Moisture-curable adhesive composition |
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US8440304B2 (en) | 2008-09-16 | 2013-05-14 | Henkel Corporation | Acrylic pressure sensitive adhesive formulation and articles comprising same |
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US20150141585A1 (en) * | 2012-05-23 | 2015-05-21 | Sika Technology Ag | Composition based on silane-terminated polymers that does not split off methanol during curing |
US9365751B2 (en) | 2012-07-24 | 2016-06-14 | Henkel IP & Holding GmbH | Reactive hot melt adhesive |
EP2948513B1 (en) | 2013-01-24 | 2019-08-07 | Henkel IP & Holding GmbH | Reactive hot melt adhesive |
DE102013216787A1 (de) * | 2013-08-23 | 2015-02-26 | Evonik Degussa Gmbh | Guanidingruppen aufweisende semi-organische Siliciumgruppen enthaltende Verbindungen |
JP6492092B2 (ja) | 2014-01-14 | 2019-03-27 | ヘンケル アイピー アンド ホールディング ゲゼルシャフト ミット ベシュレンクテル ハフツング | 改善された接着性を有する反応性ホットメルト接着剤 |
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US3471434A (en) * | 1965-12-27 | 1969-10-07 | Stauffer Chemical Co | Room temperature curing organopolysiloxane elastomers |
GB1207594A (en) * | 1967-03-16 | 1970-10-07 | Union Carbide Corp | One component room temperature vulcanizable silicon terminated polymers |
US3622529A (en) * | 1969-03-14 | 1971-11-23 | Gen Electric | Rtv silicone composition containing an imidatosilane |
US3665026A (en) * | 1969-03-14 | 1972-05-23 | Gen Electric | Imidatosilanes |
US3779794A (en) * | 1970-03-05 | 1973-12-18 | Essex Chemical Corp | Polyurethane sealant-primer system |
US3839386A (en) * | 1970-12-30 | 1974-10-01 | Stauffer Chemical Co | Oximo endblocked disiloxanes and process therefor |
US4038239A (en) * | 1973-11-23 | 1977-07-26 | Contech Inc. | Moisture curable polyurethane systems |
US3979344A (en) * | 1974-11-19 | 1976-09-07 | Inmont Corporation | Vulcanizable silicon terminated polyurethane polymer composition having improved cure speed |
US4248993A (en) * | 1977-06-29 | 1981-02-03 | Shin-Etsu Chemical Co. Ltd. | Room temperature curable organopolysiloxane |
JPS5411953A (en) * | 1977-06-29 | 1979-01-29 | Shin Etsu Chem Co Ltd | Cold-curable organopolysiloxane composition |
JPS5810431B2 (ja) * | 1978-03-30 | 1983-02-25 | 東芝シリコ−ン株式会社 | 室温硬化性ポリオルガノシロキサン組成物 |
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US4395526A (en) * | 1981-06-26 | 1983-07-26 | General Electric Company | One package, stable, moisture curable, polyalkoxy-terminated organopolysiloxane compositions and method for making |
US4469831A (en) * | 1981-08-26 | 1984-09-04 | Basf Aktiengesellschaft | Moisture-curing, storage stable, single-component polyurethane systems |
US4358575A (en) * | 1981-12-16 | 1982-11-09 | General Electric Company Silicone Products Business Division | Self-bonding one-component RTV silicone rubber compositions |
US4483972A (en) * | 1983-02-01 | 1984-11-20 | General Electric Company | Integrated cross-linkers and amine functional siloxane scavengers for RTV silicone rubber compositions |
FR2572415B1 (fr) * | 1984-10-29 | 1987-01-09 | Rhone Poulenc Spec Chim | Composition organopolysiloxanique vulcanisable a temperature ambiante en elastomere auto-adherent |
GB8510690D0 (en) * | 1985-04-26 | 1985-06-05 | Bostik Ltd | Moisture curable sealants |
US4645816A (en) * | 1985-06-28 | 1987-02-24 | Union Carbide Corporation | Novel vulcanizable silane-terminated polyurethane polymers |
JPH0618866B2 (ja) * | 1986-12-22 | 1994-03-16 | 鐘淵化学工業株式会社 | 常温硬化性樹脂の製造法 |
US4894426A (en) * | 1988-08-19 | 1990-01-16 | Basf Corporation | Fast-cure polyurethane sealant composition containing silyl-substituted piperazine accelerators |
US4954598A (en) * | 1988-10-13 | 1990-09-04 | Basf Corporation | Fast-cure polyurethane sealant composition containing silyl-substituted guanidine accelerators |
-
1990
- 1990-05-29 US US07/530,752 patent/US5097053A/en not_active Expired - Lifetime
-
1991
- 1991-04-11 CA CA002040215A patent/CA2040215A1/en not_active Abandoned
- 1991-05-23 EP EP19910108362 patent/EP0459300A3/en not_active Withdrawn
- 1991-05-24 AU AU77330/91A patent/AU7733091A/en not_active Abandoned
- 1991-05-28 BR BR919102183A patent/BR9102183A/pt not_active Application Discontinuation
- 1991-05-29 KR KR1019910008803A patent/KR910020148A/ko not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
US5097053A (en) | 1992-03-17 |
EP0459300A2 (en) | 1991-12-04 |
AU7733091A (en) | 1991-12-05 |
EP0459300A3 (en) | 1992-04-22 |
BR9102183A (pt) | 1991-12-24 |
CA2040215A1 (en) | 1991-11-30 |
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