JP2013509463A5 - - Google Patents
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- Publication number
- JP2013509463A5 JP2013509463A5 JP2012535716A JP2012535716A JP2013509463A5 JP 2013509463 A5 JP2013509463 A5 JP 2013509463A5 JP 2012535716 A JP2012535716 A JP 2012535716A JP 2012535716 A JP2012535716 A JP 2012535716A JP 2013509463 A5 JP2013509463 A5 JP 2013509463A5
- Authority
- JP
- Japan
- Prior art keywords
- adhesive according
- adhesive
- silane
- group
- meth
- Prior art date
- 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.)
- Pending
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- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 18
- 239000000853 adhesive Substances 0.000 claims description 17
- 230000001070 adhesive effect Effects 0.000 claims description 17
- 239000003054 catalyst Substances 0.000 claims description 7
- 229920000193 polymethacrylate Polymers 0.000 claims description 7
- -1 aromatic isocyanates Chemical class 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 5
- 239000002318 adhesion promoter Substances 0.000 claims description 4
- 239000000945 filler Substances 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 229910001385 heavy metal Inorganic materials 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 229910000077 silane Inorganic materials 0.000 claims description 2
- 229920005862 polyol Polymers 0.000 claims 4
- 150000003077 polyols Chemical class 0.000 claims 4
- 239000004721 Polyphenylene oxide Substances 0.000 claims 3
- 125000005442 diisocyanate group Chemical group 0.000 claims 3
- 239000012948 isocyanate Substances 0.000 claims 3
- 229920000570 polyether Polymers 0.000 claims 3
- 150000002513 isocyanates Chemical class 0.000 claims 2
- 239000004839 Moisture curing adhesive Substances 0.000 claims 1
- 229910004298 SiO 2 Inorganic materials 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 239000011111 cardboard Substances 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- BUZRAOJSFRKWPD-UHFFFAOYSA-N isocyanatosilane Chemical compound [SiH3]N=C=O BUZRAOJSFRKWPD-UHFFFAOYSA-N 0.000 claims 1
- 239000012939 laminating adhesive Substances 0.000 claims 1
- 239000000123 paper Substances 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 239000004033 plastic Substances 0.000 claims 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-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
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- 239000012975 dibutyltin dilaurate Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- YOBOXHGSEJBUPB-MTOQALJVSA-N (z)-4-hydroxypent-3-en-2-one;zirconium Chemical compound [Zr].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O YOBOXHGSEJBUPB-MTOQALJVSA-N 0.000 description 1
- TYKCBTYOMAUNLH-MTOQALJVSA-J (z)-4-oxopent-2-en-2-olate;titanium(4+) Chemical compound [Ti+4].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O TYKCBTYOMAUNLH-MTOQALJVSA-J 0.000 description 1
- SSUJUUNLZQVZMO-UHFFFAOYSA-N 1,2,3,4,8,9,10,10a-octahydropyrimido[1,2-a]azepine Chemical compound C1CCC=CN2CCCNC21 SSUJUUNLZQVZMO-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- 241000282376 Panthera tigris Species 0.000 description 1
- 229910008051 Si-OH Inorganic materials 0.000 description 1
- 229910006358 Si—OH Inorganic materials 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- NOZAQBYNLKNDRT-UHFFFAOYSA-N [diacetyloxy(ethenyl)silyl] acetate Chemical compound CC(=O)O[Si](OC(C)=O)(OC(C)=O)C=C NOZAQBYNLKNDRT-UHFFFAOYSA-N 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 150000001622 bismuth compounds Chemical class 0.000 description 1
- FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical compound [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 description 1
- NTHSYMMHMHYIJB-UHFFFAOYSA-N carbamic acid trimethoxysilane Chemical compound NC(O)=O.CO[SiH](OC)OC NTHSYMMHMHYIJB-UHFFFAOYSA-N 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 1
- JFHKCZFPXJVELF-UHFFFAOYSA-L dibutyltin(2+);2,2-diethylhexanoate Chemical compound CCCC[Sn+2]CCCC.CCCCC(CC)(CC)C([O-])=O.CCCCC(CC)(CC)C([O-])=O JFHKCZFPXJVELF-UHFFFAOYSA-L 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- LQRUPWUPINJLMU-UHFFFAOYSA-N dioctyl(oxo)tin Chemical compound CCCCCCCC[Sn](=O)CCCCCCCC LQRUPWUPINJLMU-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical class [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 1
- UWSYCPWEBZRZNJ-UHFFFAOYSA-N trimethoxy(2,4,4-trimethylpentyl)silane Chemical compound CO[Si](OC)(OC)CC(C)CC(C)(C)C UWSYCPWEBZRZNJ-UHFFFAOYSA-N 0.000 description 1
- ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009046190.6 | 2009-10-30 | ||
| DE102009046190A DE102009046190A1 (de) | 2009-10-30 | 2009-10-30 | Kaschierklebstoff mit Silanvernetzung |
| PCT/EP2010/063960 WO2011051056A1 (de) | 2009-10-30 | 2010-09-22 | Kaschierklebstoff mit silanvernetzung |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2013509463A JP2013509463A (ja) | 2013-03-14 |
| JP2013509463A5 true JP2013509463A5 (OSRAM) | 2013-11-14 |
Family
ID=43429545
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012535716A Pending JP2013509463A (ja) | 2009-10-30 | 2010-09-22 | シラン架橋を有する貼合わせ用接着剤 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20120282444A1 (OSRAM) |
| EP (1) | EP2493997A1 (OSRAM) |
| JP (1) | JP2013509463A (OSRAM) |
| KR (1) | KR20120100954A (OSRAM) |
| CN (1) | CN102597154A (OSRAM) |
| BR (1) | BR112012009223A2 (OSRAM) |
| DE (1) | DE102009046190A1 (OSRAM) |
| RU (1) | RU2012117612A (OSRAM) |
| WO (1) | WO2011051056A1 (OSRAM) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102010000881A1 (de) * | 2010-01-14 | 2011-07-21 | Henkel AG & Co. KGaA, 40589 | 1K- Kaschierklebstoff mit Silanvernetzung |
| DE102012201734A1 (de) | 2012-02-06 | 2013-08-08 | Wacker Chemie Ag | Massen auf Basis von organyloxysilanterminierten Polymeren |
| JP6095297B2 (ja) * | 2012-08-24 | 2017-03-15 | ヘンケルジャパン株式会社 | 積層シート用接着剤 |
| KR101881186B1 (ko) * | 2013-03-11 | 2018-07-23 | 동우 화인켐 주식회사 | 점착제 조성물 |
| CN103923583A (zh) * | 2014-04-11 | 2014-07-16 | 苏州之诺新材料科技有限公司 | 一种单组份端硅烷基聚丙烯酸酯胶粘剂及其制备方法 |
| CN104004488B (zh) * | 2014-04-14 | 2017-01-04 | 江苏矽时代材料科技有限公司 | 一种环保型端硅烷基丙烯酸酯改性聚氨酯电子密封胶 |
| CN106634770A (zh) * | 2016-10-26 | 2017-05-10 | 三友（天津）高分子技术有限公司 | 一种透明型单组份硅烷改性聚醚密封胶及其制备方法 |
| EP3784718B1 (en) * | 2018-04-25 | 2024-06-26 | Henkel AG & Co. KGaA | Process for the preparation of hydroxyl-functionalized polyetherpolysiloxane block copolymers |
| KR102659220B1 (ko) | 2018-04-30 | 2024-04-23 | 다우 글로벌 테크놀로지스 엘엘씨 | 이소시아네이트-말단 실란계 2액형 접착제 조성물 및 이의 제조 방법 |
| CN112029465B (zh) * | 2020-09-17 | 2022-05-17 | 郑州大学 | 一种低模量装配式建筑外墙用ms密封胶及其制备方法 |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4222925A (en) | 1978-08-02 | 1980-09-16 | Inmont Corporation | Vulcanizable silicon terminated polyurethane polymer compositions having improved cure speed |
| JP3507660B2 (ja) * | 1997-06-24 | 2004-03-15 | 積水化学工業株式会社 | 室温硬化性組成物 |
| JP3435351B2 (ja) * | 1998-07-22 | 2003-08-11 | コニシ株式会社 | 透明性に優れた湿気硬化型接着剤組成物 |
| DE19923300A1 (de) * | 1999-05-21 | 2000-11-23 | Bayer Ag | Phosphatstabilisierte, kondensationsvernetzende Polyurethanmassen, ein Verfahren zu ihrer Herstellung sowie ihre Verwendung |
| DE10132678A1 (de) | 2000-07-26 | 2002-02-07 | Henkel Kgaa | Alkoxysilylgruppenhaltige Bindemittel und Bindemittelzusammensetzungen, Verfahren zu deren Herstellung und deren Verwendung |
| US7211616B2 (en) * | 2002-02-14 | 2007-05-01 | The Glidden Company | Moisture curable adhesive |
| DE10237271A1 (de) | 2002-08-14 | 2004-03-04 | Consortium für elektrochemische Industrie GmbH | Polymermassen auf Basis alkoxysilanterminierter Polymere mit regulierbarer Härtungsgeschwindigkeit |
| DE10328844A1 (de) * | 2003-06-26 | 2005-02-03 | Consortium für elektrochemische Industrie GmbH | Alkoxysilanterminierte Prepolymere |
| JP2005023223A (ja) * | 2003-07-03 | 2005-01-27 | Konishi Co Ltd | 末端シリル基含有ポリマー型接着剤を用いたコンタクト接着方法 |
| DE10350481A1 (de) * | 2003-10-29 | 2005-06-16 | Henkel Kgaa | Festigkeitsoptimierte Polymere mit gemischten Oxyalkyleneinheiten |
| DE102005028845A1 (de) * | 2005-06-22 | 2006-12-28 | Sanofi-Aventis Deutschland Gmbh | Substituierte Heterocyclen, ihre Verwendung als Medikament sowie enthaltende pharmazeutische Zubereitungen |
| DE102005029282A1 (de) * | 2005-06-23 | 2006-12-28 | Henkel Kgaa | Silanvernetzende Kleb- und Dichtstoffmassen, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US7345130B2 (en) * | 2005-10-25 | 2008-03-18 | Dow Global Technologies Inc. | Silane functional prepolymer and isocyanate functional prepolymer blend based adhesive composition |
| JP2007162212A (ja) * | 2005-12-09 | 2007-06-28 | Sekisui Fuller Kk | 外壁構造材 |
| KR101320796B1 (ko) * | 2005-12-26 | 2013-10-22 | 아사히 가라스 가부시키가이샤 | 경화성 조성물 |
| JP5420896B2 (ja) * | 2006-02-16 | 2014-02-19 | 株式会社カネカ | 硬化性組成物 |
| JP4652277B2 (ja) * | 2006-05-18 | 2011-03-16 | 電気化学工業株式会社 | 湿気硬化型接着性組成物とスピーカの組み立て方法 |
| DE102006048041A1 (de) * | 2006-10-09 | 2008-04-10 | Henkel Kgaa | Zusammensetzungen aus teilweise silylterminierten Polymeren |
| DE102006059473A1 (de) | 2006-12-14 | 2008-06-19 | Henkel Kgaa | Silylgruppen enthaltende Mischung von Prepolymeren und deren Verwendung |
| JP5126821B2 (ja) * | 2007-07-20 | 2013-01-23 | コニシ株式会社 | 易剥離性一液湿気硬化型接着剤 |
| JP5421106B2 (ja) * | 2007-07-24 | 2014-02-19 | 株式会社カネカ | 硬化性組成物 |
| DE102008003743A1 (de) * | 2008-01-10 | 2009-07-16 | Henkel Ag & Co. Kgaa | Härtbare Zusammensetzungen enthaltend weichelastische silylierte Polyurethane |
| DE102008025575A1 (de) * | 2008-05-28 | 2009-12-03 | Evonik Röhm Gmbh | Mit Wasser vernetzbare Dichtmasse |
| DE102008002016A1 (de) | 2008-05-28 | 2009-12-03 | Evonik Röhm Gmbh | Verfahren zur Herstellung von silyl-funktionalisierten ABA-Triblockcopolymeren auf (Meth)acrylatbasis |
| DE102008032580A1 (de) * | 2008-07-11 | 2010-01-14 | Henkel Ag & Co. Kgaa | Härtbare Zusammensetzungen |
-
2009
- 2009-10-30 DE DE102009046190A patent/DE102009046190A1/de not_active Ceased
-
2010
- 2010-09-22 JP JP2012535716A patent/JP2013509463A/ja active Pending
- 2010-09-22 WO PCT/EP2010/063960 patent/WO2011051056A1/de not_active Ceased
- 2010-09-22 KR KR1020127010922A patent/KR20120100954A/ko not_active Withdrawn
- 2010-09-22 RU RU2012117612/05A patent/RU2012117612A/ru not_active Application Discontinuation
- 2010-09-22 EP EP10757090A patent/EP2493997A1/de not_active Withdrawn
- 2010-09-22 BR BR112012009223A patent/BR112012009223A2/pt not_active IP Right Cessation
- 2010-09-22 CN CN201080048708.4A patent/CN102597154A/zh active Pending
-
2012
- 2012-04-30 US US13/460,068 patent/US20120282444A1/en not_active Abandoned
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