JP2013512997A5 - - Google Patents
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- Publication number
- JP2013512997A5 JP2013512997A5 JP2012542155A JP2012542155A JP2013512997A5 JP 2013512997 A5 JP2013512997 A5 JP 2013512997A5 JP 2012542155 A JP2012542155 A JP 2012542155A JP 2012542155 A JP2012542155 A JP 2012542155A JP 2013512997 A5 JP2013512997 A5 JP 2013512997A5
- Authority
- JP
- Japan
- Prior art keywords
- composition
- polyamine
- moiety
- epoxy resin
- amine
- 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.)
- Ceased
Links
- 239000000203 mixture Substances 0.000 claims description 17
- 239000003822 epoxy resin Substances 0.000 claims description 15
- 229920000768 polyamine Polymers 0.000 claims description 15
- 229920000647 polyepoxide Polymers 0.000 claims description 15
- 239000003054 catalyst Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- VUEDNLCYHKSELL-UHFFFAOYSA-N arsonium Chemical group [AsH4+] VUEDNLCYHKSELL-UHFFFAOYSA-N 0.000 claims description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphine group Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 2
- 125000005496 phosphonium group Chemical group 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 4
- 150000002118 epoxides Chemical class 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- YDIZFUMZDHUHSH-UHFFFAOYSA-N 1,7-bis(ethenyl)-3,8-dioxatricyclo[5.1.0.02,4]oct-5-ene Chemical group C12OC2C=CC2(C=C)C1(C=C)O2 YDIZFUMZDHUHSH-UHFFFAOYSA-N 0.000 claims 2
- 125000003277 amino group Chemical group 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- -1 amine compounds Chemical class 0.000 description 6
- 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 5
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 229940043237 diethanolamine Drugs 0.000 description 2
- XBTRYWRVOBZSGM-UHFFFAOYSA-N (4-methylphenyl)methanediamine Chemical compound CC1=CC=C(C(N)N)C=C1 XBTRYWRVOBZSGM-UHFFFAOYSA-N 0.000 description 1
- 0 **(C=C)C(CCCC1)=C1C=C Chemical compound **(C=C)C(CCCC1)=C1C=C 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 description 1
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 description 1
- WFCSWCVEJLETKA-UHFFFAOYSA-N 2-piperazin-1-ylethanol Chemical compound OCCN1CCNCC1 WFCSWCVEJLETKA-UHFFFAOYSA-N 0.000 description 1
- 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 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000003974 aralkylamines Chemical class 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- KXHPPCXNWTUNSB-UHFFFAOYSA-M benzyl(trimethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1=CC=CC=C1 KXHPPCXNWTUNSB-UHFFFAOYSA-M 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- GELSOTNVVKOYAW-UHFFFAOYSA-N ethyl(triphenyl)phosphanium Chemical compound C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CC)C1=CC=CC=C1 GELSOTNVVKOYAW-UHFFFAOYSA-N 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26637609P | 2009-12-03 | 2009-12-03 | |
| US61/266,376 | 2009-12-03 | ||
| PCT/US2010/058543 WO2011068858A1 (en) | 2009-12-03 | 2010-12-01 | Adducts based on divinylarene oxides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2013512997A JP2013512997A (ja) | 2013-04-18 |
| JP2013512997A5 true JP2013512997A5 (enExample) | 2014-01-23 |
Family
ID=43759616
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012542155A Ceased JP2013512997A (ja) | 2009-12-03 | 2010-12-01 | ジビニルアレーンジオキシドに基づく付加物 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20120245306A1 (enExample) |
| EP (1) | EP2507284A1 (enExample) |
| JP (1) | JP2013512997A (enExample) |
| KR (1) | KR20120089367A (enExample) |
| CN (1) | CN102648229A (enExample) |
| BR (1) | BR112012011527A2 (enExample) |
| TW (1) | TW201136974A (enExample) |
| WO (1) | WO2011068858A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2803289A1 (en) * | 2010-06-23 | 2011-12-29 | Dow Global Technologies Llc | Powder coatings compositions |
| MX2014003538A (es) * | 2011-09-21 | 2014-07-14 | Dow Global Technologies Llc | Composiciones de resina epoxi-funcional. |
| US9605161B2 (en) * | 2012-06-15 | 2017-03-28 | Blue Cube Ip Llc | Conductive carbonized layered article |
| CN104364297B (zh) * | 2012-06-15 | 2016-08-24 | 蓝立方知识产权有限责任公司 | 碳前体组合物 |
| CN109401200A (zh) * | 2018-10-29 | 2019-03-01 | 江苏宏鹏电气科技有限公司 | 一种用于母线槽内绝缘衬垫材料的制备配方 |
| WO2025075950A1 (en) * | 2023-10-03 | 2025-04-10 | Westlake Epoxy Inc. | Epoxy renin compositions and methods of producing thereof |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2901461A (en) | 1955-05-05 | 1959-08-25 | Union Carbide Corp | Curable glycidyl polyether-polyamine compositions |
| US3018262A (en) | 1957-05-01 | 1962-01-23 | Shell Oil Co | Curing polyepoxides with certain metal salts of inorganic acids |
| GB854679A (en) * | 1958-10-11 | 1960-11-23 | Union Carbide Corp | Improvements in and relating to polymerisable epoxide compositions |
| US2912389A (en) | 1957-08-08 | 1959-11-10 | Union Carbide Corp | Polymers of divinylbenzene dioxide |
| US2924580A (en) * | 1957-08-08 | 1960-02-09 | Union Carbide Corp | Divinyl benzene dioxide compositions |
| US3496138A (en) * | 1966-08-01 | 1970-02-17 | Union Carbide Corp | Adducts of polyglycol diamines and curable compositions comprising polyepoxides and said adducts |
| US3773790A (en) * | 1969-11-26 | 1973-11-20 | Ajinomoto Kk | Spiroacetal diamine-epoxide liquid as curing agent for epoxy resins |
| DE3328134C2 (de) * | 1983-08-04 | 1986-08-07 | Hüls AG, 4370 Marl | EP-Pulverlacke und Verfahren zur Herstellung matter Überzüge |
| US4925901A (en) | 1988-02-12 | 1990-05-15 | The Dow Chemical Company | Latent, curable, catalyzed mixtures of epoxy-containing and phenolic hydroxyl-containing compounds |
| US5135993A (en) | 1990-09-11 | 1992-08-04 | Dow Corning Corporation | High modulus silicones as toughening agents for epoxy resins |
| GB9411367D0 (en) | 1994-06-07 | 1994-07-27 | Ici Composites Inc | Curable Composites |
| US6153719A (en) | 1998-02-04 | 2000-11-28 | Lord Corporation | Thiol-cured epoxy composition |
| US6632893B2 (en) | 1999-05-28 | 2003-10-14 | Henkel Loctite Corporation | Composition of epoxy resin, cyanate ester, imidazole and polysulfide tougheners |
| IL138474A0 (en) | 2000-09-14 | 2001-10-31 | Epox Ltd | Highly branched water-soluble polyamine oligomers, process for their preparation and applications thereof |
| US6572971B2 (en) | 2001-02-26 | 2003-06-03 | Ashland Chemical | Structural modified epoxy adhesive compositions |
| US6632860B1 (en) | 2001-08-24 | 2003-10-14 | Texas Research International, Inc. | Coating with primer and topcoat both containing polysulfide, epoxy resin and rubber toughener |
| GB0212062D0 (en) | 2002-05-24 | 2002-07-03 | Vantico Ag | Jetable compositions |
| US7163973B2 (en) | 2002-08-08 | 2007-01-16 | Henkel Corporation | Composition of bulk filler and epoxy-clay nanocomposite |
| US7001938B2 (en) | 2003-01-27 | 2006-02-21 | Resolution Performance Products Llc | Epoxy resin curing compositions and resin compositions including same |
| US6887574B2 (en) | 2003-06-06 | 2005-05-03 | Dow Global Technologies Inc. | Curable flame retardant epoxy compositions |
| CN103554184A (zh) | 2004-05-28 | 2014-02-05 | 陶氏环球技术有限责任公司 | 可用于制造无卤素抗引燃聚合物的含磷化合物 |
| ES2337598T3 (es) | 2004-11-10 | 2010-04-27 | Dow Global Technologies Inc. | Resinas espoxi endurecidas con copolimeros de bloques anfifilicos y estratificados electricos fabricados a partir de ellas. |
| US8048819B2 (en) | 2005-06-23 | 2011-11-01 | Momentive Performance Materials Inc. | Cure catalyst, composition, electronic device and associated method |
| EP2384345B1 (en) * | 2008-12-30 | 2013-05-29 | Dow Global Technologies LLC | Divinylarene dioxide formulations for vacuum resin infusion molding |
-
2010
- 2010-12-01 CN CN2010800551521A patent/CN102648229A/zh active Pending
- 2010-12-01 US US13/503,662 patent/US20120245306A1/en not_active Abandoned
- 2010-12-01 EP EP10787239A patent/EP2507284A1/en not_active Withdrawn
- 2010-12-01 JP JP2012542155A patent/JP2013512997A/ja not_active Ceased
- 2010-12-01 WO PCT/US2010/058543 patent/WO2011068858A1/en not_active Ceased
- 2010-12-01 KR KR1020127017208A patent/KR20120089367A/ko not_active Withdrawn
- 2010-12-01 BR BR112012011527A patent/BR112012011527A2/pt not_active IP Right Cessation
- 2010-12-02 TW TW099141872A patent/TW201136974A/zh unknown
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