JP2005519175A5 - - Google Patents
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- JP2005519175A5 JP2005519175A5 JP2003574699A JP2003574699A JP2005519175A5 JP 2005519175 A5 JP2005519175 A5 JP 2005519175A5 JP 2003574699 A JP2003574699 A JP 2003574699A JP 2003574699 A JP2003574699 A JP 2003574699A JP 2005519175 A5 JP2005519175 A5 JP 2005519175A5
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- 239000000203 mixture Substances 0.000 claims description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- -1 borane amine Chemical class 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 239000011593 sulfur Substances 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 239000000758 substrate Substances 0.000 claims 7
- 239000007788 liquid Substances 0.000 claims 5
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 238000006116 polymerization reaction Methods 0.000 claims 4
- 238000007142 ring opening reaction Methods 0.000 claims 4
- 239000000853 adhesive Substances 0.000 claims 3
- 230000001070 adhesive effect Effects 0.000 claims 3
- 239000008199 coating composition Substances 0.000 claims 2
- 230000000977 initiatory effect Effects 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 229910000085 borane Inorganic materials 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 239000011968 lewis acid catalyst Substances 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- 238000010526 radical polymerization reaction Methods 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 claims 1
- UORVGPXVDQYIDP-UHFFFAOYSA-N trihydridoboron Substances B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 6
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 3
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 3
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 2
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 2
- 229910015900 BF3 Inorganic materials 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- 239000005058 Isophorone diisocyanate Substances 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 2
- 229920010524 Syndiotactic polystyrene Polymers 0.000 description 2
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 2
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- KFYRJJBUHYILSO-YFKPBYRVSA-N (2s)-2-amino-3-dimethylarsanylsulfanyl-3-methylbutanoic acid Chemical compound C[As](C)SC(C)(C)[C@@H](N)C(O)=O KFYRJJBUHYILSO-YFKPBYRVSA-N 0.000 description 1
- OUPZKGBUJRBPGC-UHFFFAOYSA-N 1,3,5-tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound O=C1N(CC2OC2)C(=O)N(CC2OC2)C(=O)N1CC1CO1 OUPZKGBUJRBPGC-UHFFFAOYSA-N 0.000 description 1
- ZQXCQTAELHSNAT-UHFFFAOYSA-N 1-chloro-3-nitro-5-(trifluoromethyl)benzene Chemical compound [O-][N+](=O)C1=CC(Cl)=CC(C(F)(F)F)=C1 ZQXCQTAELHSNAT-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- SOGGLVJYVOCYTB-UHFFFAOYSA-N 3-(oxiran-2-yl)propan-1-ol Chemical compound OCCCC1CO1 SOGGLVJYVOCYTB-UHFFFAOYSA-N 0.000 description 1
- FAXDZWQIWUSWJH-UHFFFAOYSA-N 3-methoxypropan-1-amine Chemical compound COCCCN FAXDZWQIWUSWJH-UHFFFAOYSA-N 0.000 description 1
- MECNWXGGNCJFQJ-UHFFFAOYSA-N 3-piperidin-1-ylpropane-1,2-diol Chemical group OCC(O)CN1CCCCC1 MECNWXGGNCJFQJ-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical group FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- PGLIUCLTXOYQMV-UHFFFAOYSA-N Cetirizine hydrochloride Chemical compound Cl.Cl.C1CN(CCOCC(=O)O)CCN1C(C=1C=CC(Cl)=CC=1)C1=CC=CC=C1 PGLIUCLTXOYQMV-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical group OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- 101100456571 Mus musculus Med12 gene Proteins 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- KAPCRJOPWXUMSQ-UHFFFAOYSA-N [2,2-bis[3-(aziridin-1-yl)propanoyloxymethyl]-3-hydroxypropyl] 3-(aziridin-1-yl)propanoate Chemical compound C1CN1CCC(=O)OCC(COC(=O)CCN1CC1)(CO)COC(=O)CCN1CC1 KAPCRJOPWXUMSQ-UHFFFAOYSA-N 0.000 description 1
- OEOQTSUNXODXQL-UHFFFAOYSA-N [2-[3-(2-methylaziridin-1-yl)propanoyloxy]-2-[3-(2-methylaziridin-1-yl)propanoyloxymethyl]butyl] 3-(2-methylaziridin-1-yl)propanoate Chemical compound C1C(C)N1CCC(=O)OCC(OC(=O)CCN1C(C1)C)(CC)COC(=O)CCN1CC1C OEOQTSUNXODXQL-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229940106691 bisphenol a Drugs 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- QXJJQWWVWRCVQT-UHFFFAOYSA-K calcium;sodium;phosphate Chemical compound [Na+].[Ca+2].[O-]P([O-])([O-])=O QXJJQWWVWRCVQT-UHFFFAOYSA-K 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000011258 core-shell material Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- RBQRWNWVPQDTJJ-UHFFFAOYSA-N methacryloyloxyethyl isocyanate Chemical compound CC(=C)C(=O)OCCN=C=O RBQRWNWVPQDTJJ-UHFFFAOYSA-N 0.000 description 1
- SWVGZFQJXVPIKM-UHFFFAOYSA-N n,n-bis(methylamino)propan-1-amine Chemical compound CCCN(NC)NC SWVGZFQJXVPIKM-UHFFFAOYSA-N 0.000 description 1
- VULHYRAYXYTONQ-UHFFFAOYSA-N n-phenylmethanimine Chemical compound C=NC1=CC=CC=C1 VULHYRAYXYTONQ-UHFFFAOYSA-N 0.000 description 1
- CHNLPLHJUPMEOI-UHFFFAOYSA-N oxolane;trifluoroborane Chemical compound FB(F)F.C1CCOC1 CHNLPLHJUPMEOI-UHFFFAOYSA-N 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Substances C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- KCNSDMPZCKLTQP-UHFFFAOYSA-N tetraphenylen-1-ol Chemical compound C12=CC=CC=C2C2=CC=CC=C2C2=CC=CC=C2C2=C1C=CC=C2O KCNSDMPZCKLTQP-UHFFFAOYSA-N 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- CMHHITPYCHHOGT-UHFFFAOYSA-N tributylborane Chemical group CCCCB(CCCC)CCCC CMHHITPYCHHOGT-UHFFFAOYSA-N 0.000 description 1
- LALRXNPLTWZJIJ-UHFFFAOYSA-N triethylborane Chemical group CCB(CC)CC LALRXNPLTWZJIJ-UHFFFAOYSA-N 0.000 description 1
- DSROZUMNVRXZNO-UHFFFAOYSA-K tris[(1-naphthalen-1-yl-3-phenylnaphthalen-2-yl)oxy]alumane Chemical compound C=1C=CC=CC=1C=1C=C2C=CC=CC2=C(C=2C3=CC=CC=C3C=CC=2)C=1O[Al](OC=1C(=C2C=CC=CC2=CC=1C=1C=CC=CC=1)C=1C2=CC=CC=C2C=CC=1)OC(C(=C1C=CC=CC1=C1)C=2C3=CC=CC=C3C=CC=2)=C1C1=CC=CC=C1 DSROZUMNVRXZNO-UHFFFAOYSA-K 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/095,326 US6762260B2 (en) | 2002-03-05 | 2002-03-05 | Organoborane amine complex polymerization initiators and polymerizable compositions |
| PCT/US2003/006444 WO2003076485A2 (en) | 2002-03-05 | 2003-03-03 | Organoborane amine complex polymerization initiators and polymerizable compositions |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005519175A JP2005519175A (ja) | 2005-06-30 |
| JP2005519175A5 true JP2005519175A5 (enExample) | 2006-03-23 |
| JP4373222B2 JP4373222B2 (ja) | 2009-11-25 |
Family
ID=27804267
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003574699A Expired - Fee Related JP4373222B2 (ja) | 2002-03-05 | 2003-03-03 | 有機ボランアミン錯体重合開始剤及び重合性組成物 |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US6762260B2 (enExample) |
| EP (1) | EP1483304B1 (enExample) |
| JP (1) | JP4373222B2 (enExample) |
| KR (1) | KR20040095258A (enExample) |
| CN (1) | CN100338110C (enExample) |
| AT (1) | ATE420124T1 (enExample) |
| AU (1) | AU2003219986A1 (enExample) |
| BR (1) | BR0308306A (enExample) |
| CA (1) | CA2478084A1 (enExample) |
| DE (1) | DE60325704D1 (enExample) |
| ES (1) | ES2316742T3 (enExample) |
| IN (1) | IN2004CH01924A (enExample) |
| PT (1) | PT1483304E (enExample) |
| RU (1) | RU2315065C9 (enExample) |
| WO (1) | WO2003076485A2 (enExample) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1398332A4 (en) * | 2001-04-27 | 2006-05-03 | Daicel Chem | POLY (METH) ACRYLAMIDE HIGH STEREO REGULARITY AND METHOD FOR THE PRODUCTION THEREOF |
| IE20020293A1 (en) * | 2002-04-23 | 2003-10-29 | Loctite R & D Ltd | Initiator systems, polymerisable compositions, and uses thereof for bonding low surface energy substrates |
| DE10302416A1 (de) * | 2003-01-21 | 2004-07-29 | Röhm GmbH & Co. KG | Matter Polymerisationsklebstoff |
| US6777512B1 (en) * | 2003-02-28 | 2004-08-17 | Dow Global Technologies Inc. | Amine organoborane complex initiated polymerizable compositions containing siloxane polymerizable components |
| EP1648944A1 (en) * | 2003-06-09 | 2006-04-26 | The Dow Global Technologies Inc. | Stabilized organoborane polymerization initiators and polymerizable compositions |
| CN1835992B (zh) * | 2003-08-13 | 2010-10-06 | 陶氏环球技术公司 | 使基材与物体接合的方法 |
| WO2005017005A1 (en) * | 2003-08-13 | 2005-02-24 | Dow Global Technologies Inc. | Method for joining substrates and objects |
| DE10345045A1 (de) * | 2003-09-26 | 2005-04-14 | Röhm GmbH & Co. KG | Verfahren zur Oberflächenvergütung von Werkstoffen durch Aufbringen insbesondere transparenter Schichten auf Basis von Polymethacrylaten |
| US8501886B2 (en) * | 2003-12-22 | 2013-08-06 | Dow Global Technologies Llc | Accelerated organoborane amine complex initiated polymerizable compositions |
| WO2005063480A1 (en) * | 2003-12-22 | 2005-07-14 | Dow Global Technologies Inc. | Accelerated organoborane amine complex initiated polymerizable compositions |
| JP2008502742A (ja) * | 2004-06-09 | 2008-01-31 | ダウ グローバル テクノロジーズ インコーポレイティド | 安定化有機ボラン重合開始剤及び重合性組成物 |
| US7850870B2 (en) * | 2004-10-28 | 2010-12-14 | Dow Corning Corporation | Conductive curable compositions |
| US8202932B2 (en) * | 2004-12-03 | 2012-06-19 | Loctite (R&D) Limited | Adhesive bonding systems having adherence to low energy surfaces |
| JP5090182B2 (ja) * | 2005-01-04 | 2012-12-05 | ダウ・コーニング・コーポレイション | オルガノボランアミン錯体によって硬化されたシロキサンおよびシラン |
| DE602005015766D1 (de) * | 2005-01-04 | 2009-09-10 | Dow Corning | Organosiliciumfunktionelle bor-amin-katalysatorkomplexe und daraus hergestellte härtbare zusammensetzungen |
| JP5039567B2 (ja) | 2005-02-16 | 2012-10-03 | ダウ・コーニング・コーポレイション | ポリマー粒子、および、有機ボランアミン錯体を用いた封入（ｅｎｃａｐｓｕｌａｔｅｄ）組成物 |
| US8048819B2 (en) * | 2005-06-23 | 2011-11-01 | Momentive Performance Materials Inc. | Cure catalyst, composition, electronic device and associated method |
| CN101267949A (zh) * | 2005-09-21 | 2008-09-17 | 陶氏康宁公司 | 使用有机基硼烷胺络合物的环境平版印刷方法 |
| CN101501043A (zh) | 2005-10-07 | 2009-08-05 | 陶氏环球技术公司 | 酰胺-有机硼酸酯引发剂体系 |
| US7682663B2 (en) * | 2006-02-23 | 2010-03-23 | Bowling Green State University | Remote curing of polymer coating by gaseous, vaporous or aerosol initiating agent |
| CN101448573B (zh) * | 2006-05-23 | 2012-05-23 | 陶氏康宁公司 | 具有酰胺官能的聚合物的硼烷催化剂络合物和由其制备的可固化的组合物 |
| CN101506308B (zh) * | 2006-06-20 | 2011-09-14 | 道康宁公司 | 可固化有机硅组合物 |
| US7887668B2 (en) * | 2006-08-30 | 2011-02-15 | Dow Global Technologies Inc. | Amine organoborane polymerizable compostion and uses therefor |
| US7524907B2 (en) * | 2006-10-12 | 2009-04-28 | Dow Global Technologies, Inc. | Accelerated organoborane initiated polymerizable compositions |
| US20080103274A1 (en) * | 2006-10-12 | 2008-05-01 | Jialanella Gary L | Accelerated organoborane initiated polymerizable compositions |
| DE102007032836A1 (de) * | 2007-07-12 | 2009-01-15 | Evonik Röhm Gmbh | Emulsionspolymerisat enthaltend Aktivatoren, Verfahren zu dessen Herstellung sowie dessen Verwendung in Zwei- oder Mehrkomponentensystemen |
| US8377852B2 (en) * | 2007-10-26 | 2013-02-19 | Dow Corning Corporation | Method of preparing a substrate with a composition including an organoborane initiator |
| US8742050B2 (en) | 2008-03-28 | 2014-06-03 | Henkel US IP LLC | Two part hybrid adhesive |
| US20110104508A1 (en) * | 2008-08-29 | 2011-05-05 | Dow Global Technologies Inc. | Adhesive for bonding to flexible polymer surfaces |
| BRPI0914446A2 (pt) * | 2008-10-23 | 2015-10-27 | Dow Global Technologies Llc | complexo de organoborano |
| EP2393855B1 (en) * | 2009-02-04 | 2015-06-17 | Dow Corning Corporation | Method of forming a non-random copolymer |
| WO2010149637A1 (en) | 2009-06-26 | 2010-12-29 | Basf Se | Method of curing a coating composition comprising a radical curable compound and an organoborane-amine complex |
| KR101867786B1 (ko) * | 2009-06-26 | 2018-06-15 | 바스프 코팅스 게엠베하 | 페인트 코팅계 및 다층 페인트 코팅의 제조 방법 |
| JP5598109B2 (ja) * | 2010-06-17 | 2014-10-01 | ソニー株式会社 | 音響変換装置 |
| JP5540920B2 (ja) * | 2010-06-17 | 2014-07-02 | ソニー株式会社 | 音響変換装置 |
| JP5540921B2 (ja) * | 2010-06-17 | 2014-07-02 | ソニー株式会社 | 音響変換装置 |
| WO2013156892A1 (en) * | 2012-04-20 | 2013-10-24 | Basf Se | Process for graft polymerization on polymer surfaces using organoborane-amine complexes as radical initiators |
| JP2017149789A (ja) * | 2014-07-03 | 2017-08-31 | 株式会社イーテック | ２液混合型接着剤 |
| EP3183311A1 (en) | 2014-08-18 | 2017-06-28 | LORD Corporation | Method for low temperature bonding of elastomers |
| WO2019116201A1 (en) | 2017-12-13 | 2019-06-20 | 3M Innovative Properties Company | Optically clear adhesives containing a trialkyl borane complex initiator and photoacid |
| US11667734B2 (en) | 2019-02-14 | 2023-06-06 | Drexel University | Oxygen tolerant and room temperature raft through alkylborane initiation |
| EP3719088B1 (en) * | 2019-04-02 | 2024-09-04 | 3M Innovative Properties Company | Curable precursor of a structural adhesive composition |
| EP3719089B1 (en) * | 2019-04-02 | 2024-07-31 | 3M Innovative Properties Company | Process of manufacturing a curable precursor of a structural adhesive composition |
| EP4192914A1 (en) | 2020-08-05 | 2023-06-14 | Greenseal NV | Polymerizable foam composition curable by oxygen |
Family Cites Families (44)
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-
2002
- 2002-03-05 US US10/095,326 patent/US6762260B2/en not_active Expired - Fee Related
-
2003
- 2003-03-03 PT PT03716274T patent/PT1483304E/pt unknown
- 2003-03-03 DE DE60325704T patent/DE60325704D1/de not_active Expired - Lifetime
- 2003-03-03 ES ES03716274T patent/ES2316742T3/es not_active Expired - Lifetime
- 2003-03-03 JP JP2003574699A patent/JP4373222B2/ja not_active Expired - Fee Related
- 2003-03-03 AU AU2003219986A patent/AU2003219986A1/en not_active Abandoned
- 2003-03-03 CN CNB03805373XA patent/CN100338110C/zh not_active Expired - Fee Related
- 2003-03-03 EP EP03716274A patent/EP1483304B1/en not_active Expired - Lifetime
- 2003-03-03 AT AT03716274T patent/ATE420124T1/de not_active IP Right Cessation
- 2003-03-03 KR KR20047013772A patent/KR20040095258A/ko not_active Ceased
- 2003-03-03 RU RU2004129585A patent/RU2315065C9/ru not_active IP Right Cessation
- 2003-03-03 CA CA 2478084 patent/CA2478084A1/en not_active Abandoned
- 2003-03-03 WO PCT/US2003/006444 patent/WO2003076485A2/en not_active Ceased
- 2003-03-03 BR BR0308306A patent/BR0308306A/pt not_active Application Discontinuation
- 2003-10-14 US US10/685,152 patent/US20040082743A1/en not_active Abandoned
-
2004
- 2004-08-30 IN IN1924CH2004 patent/IN2004CH01924A/en unknown
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