JP2013513011A5 - - Google Patents
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- Publication number
- JP2013513011A5 JP2013513011A5 JP2012543125A JP2012543125A JP2013513011A5 JP 2013513011 A5 JP2013513011 A5 JP 2013513011A5 JP 2012543125 A JP2012543125 A JP 2012543125A JP 2012543125 A JP2012543125 A JP 2012543125A JP 2013513011 A5 JP2013513011 A5 JP 2013513011A5
- Authority
- JP
- Japan
- Prior art keywords
- resin composition
- acid
- dioxide
- mass
- functional polyester
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 claims description 13
- 239000003822 epoxy resin Substances 0.000 claims description 9
- 229920000647 polyepoxide Polymers 0.000 claims description 9
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 7
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 4
- -1 carboxy ester Chemical class 0.000 claims description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 4
- 239000001361 adipic acid Substances 0.000 claims description 2
- 235000011037 adipic acid Nutrition 0.000 claims description 2
- 239000011342 resin composition Substances 0.000 claims 10
- 229920001225 polyester resin Polymers 0.000 claims 6
- 239000004645 polyester resin Substances 0.000 claims 6
- 239000003795 chemical substances by application Substances 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 3
- 239000003054 catalyst Substances 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
- ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 2-phenyl-1h-imidazole Chemical compound C1=CNC(C=2C=CC=CC=2)=N1 ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 0.000 claims 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims 2
- 239000007795 chemical reaction product Substances 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 229920005989 resin Polymers 0.000 claims 2
- 239000011347 resin Substances 0.000 claims 2
- ILSRXKFYTXYKJS-UHFFFAOYSA-N 2,4-bis(ethenyl)-3,6-dioxatetracyclo[6.4.0.02,4.05,7]dodeca-1(12),8,10-triene Chemical compound C=CC12OC1(C=C)C1=CC=CC=C1C1C2O1 ILSRXKFYTXYKJS-UHFFFAOYSA-N 0.000 claims 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 claims 1
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 claims 1
- GLPDXGJXUWGMQJ-UHFFFAOYSA-N 4-ethenyl-7-(4-ethenylphenyl)-3,8-dioxatricyclo[5.1.0.02,4]oct-5-ene Chemical compound C(=C)C1=CC=C(C=C1)C12C(C3C(C=C1)(C=C)O3)O2 GLPDXGJXUWGMQJ-UHFFFAOYSA-N 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- 239000004593 Epoxy Substances 0.000 claims 1
- 239000004640 Melamine resin Substances 0.000 claims 1
- 229920000877 Melamine resin Polymers 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- SRWLXBHGOYPTCM-UHFFFAOYSA-M acetic acid;ethyl(triphenyl)phosphanium;acetate Chemical group CC(O)=O.CC([O-])=O.C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CC)C1=CC=CC=C1 SRWLXBHGOYPTCM-UHFFFAOYSA-M 0.000 claims 1
- 150000008065 acid anhydrides Chemical class 0.000 claims 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 claims 1
- 229940092714 benzenesulfonic acid Drugs 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 239000007809 chemical reaction catalyst Substances 0.000 claims 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 claims 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Natural products C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 150000002989 phenols Chemical class 0.000 claims 1
- 229920005862 polyol Polymers 0.000 claims 1
- 150000003077 polyols Chemical class 0.000 claims 1
- 239000000047 product Substances 0.000 claims 1
- 229920003987 resole Polymers 0.000 claims 1
- BRKFQVAOMSWFDU-UHFFFAOYSA-M tetraphenylphosphanium;bromide Chemical compound [Br-].C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 BRKFQVAOMSWFDU-UHFFFAOYSA-M 0.000 claims 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 claims 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 claims 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 1
- 150000001991 dicarboxylic acids Chemical class 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
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 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
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26767209P | 2009-12-08 | 2009-12-08 | |
| US61/267,672 | 2009-12-08 | ||
| PCT/US2010/056214 WO2011071650A1 (en) | 2009-12-08 | 2010-11-10 | Hydroxyl-functional polyester resins |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013513011A JP2013513011A (ja) | 2013-04-18 |
| JP2013513011A5 true JP2013513011A5 (https=) | 2013-12-26 |
| JP5902625B2 JP5902625B2 (ja) | 2016-04-13 |
Family
ID=43477956
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012543125A Expired - Fee Related JP5902625B2 (ja) | 2009-12-08 | 2010-11-10 | ヒドロキシル官能性ポリエステル樹脂 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8975343B2 (https=) |
| EP (1) | EP2510035B1 (https=) |
| JP (1) | JP5902625B2 (https=) |
| KR (1) | KR20120114296A (https=) |
| CN (1) | CN102666636B (https=) |
| BR (1) | BR112012013135A8 (https=) |
| TW (1) | TWI503341B (https=) |
| WO (1) | WO2011071650A1 (https=) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2012013529A (es) * | 2010-05-21 | 2013-01-24 | Dow Global Technologies Llc | Composiciones curables. |
| US9040636B2 (en) * | 2011-12-15 | 2015-05-26 | Dow Global Technologies Llc | Hydroxy ester resins |
| US20140336302A1 (en) * | 2011-12-29 | 2014-11-13 | Dow Global Technologies Llc | Curable water soluble epoxy acrylate resin compositions |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US163973A (en) | 1875-06-01 | Improvement in indexes | ||
| US3018262A (en) | 1957-05-01 | 1962-01-23 | Shell Oil Co | Curing polyepoxides with certain metal salts of inorganic acids |
| US2924580A (en) * | 1957-08-08 | 1960-02-09 | Union Carbide Corp | Divinyl benzene dioxide compositions |
| GB866410A (en) * | 1958-10-11 | 1961-04-26 | Union Carbide Corp | Improvements in and relating to polymerisable epoxide compositions |
| DE1227659B (de) * | 1958-10-13 | 1966-10-27 | Union Carbide Corp | Verfahren zur Herstellung von Formteilen |
| EP0205402B1 (de) * | 1985-06-06 | 1990-05-23 | Ciba-Geigy Ag | 2,6-Disubstituierte 4-Epoxypropylphenylglycidylether und deren Verwendung |
| 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 |
| US5780582A (en) | 1996-12-31 | 1998-07-14 | The Dow Chemical Company | Hydroxy-functionalized polyester and poly(ester ether) oligomers |
| KR20010012221A (ko) * | 1997-05-06 | 2001-02-15 | 베르너 훽스트, 지크프리트 포트호프 | 개질된 에폭시 수지 및 열경화성 조성물, 특히 분말코팅용 배합 성분으로서 그의 용도 |
| AU711786B2 (en) * | 1997-05-16 | 1999-10-21 | National Starch And Chemical Investment Holding Corporation | Reactive radiation- or thermally-initiated cationically- curable epoxide monomers and compositions made from those monomers |
| ES2126545T1 (es) * | 1997-05-16 | 1999-04-01 | Nat Starch Chem Invest | Monomeros de epoxido reactivos curables cationicamente iniciados termicamente o por radiacion, y composiciones realizadas a partir de estos monomeros. |
| 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 |
| 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 |
| US6887574B2 (en) | 2003-06-06 | 2005-05-03 | Dow Global Technologies Inc. | Curable flame retardant epoxy compositions |
| BRPI0510861A (pt) | 2004-05-28 | 2007-12-26 | Dow Global Technologies Inc | processo para preparar um composto contendo fósforo, processo para preparar uma composição contendo fósforo, processo para preparar um composto de resina epóxi contendo fósforo, processo para preparar uma composição de resina epóxi contendo fósforo , processo para preparar um composto contendo um anel de benzoxazina e fósforo, processo para preparar uma composição de resina contendo anel de benzoxazina e fósforo, processo para preparar um composto contendo grupo termolábil e fósforo, processo para preparar uma composição de resina termolábil contendo fósforo, composto contendo fósforo, composição contendo fósforo, composição de resina epóxi contendo fósforo, composição contendo fósforo, composto de resina epóxi contendo fósforo, composto contendo anel de benzoxazina e fósforo, composição de resina contendo anel de benzoxazina e fósforo, composto contendo grupo termolábil e fósforo, composição de resina termolábil contendo fósforo, produto obtenìvel, composição de resina epóxi resistente à chama, composto de epóxi, composição de resina epóxi resistente a chama, composição de cura resistente à ignição, pré-impregnado, laminado, placa de circuito, poliol, resina de poliuretano resistente à chama, composição termoplástica resistente à ignição, composição hìbrida termoplástica / termofixa resistente à ignição e composição de revestimento |
| MX2007005597A (es) | 2004-11-10 | 2007-05-23 | Dow Global Technologies Inc | Resinas epoxicas endurecidas con copolimero de bloque anfifilico y laminados electricos hechos de las mismas. |
| US8048819B2 (en) | 2005-06-23 | 2011-11-01 | Momentive Performance Materials Inc. | Cure catalyst, composition, electronic device and associated method |
| TW200835712A (en) | 2006-10-10 | 2008-09-01 | Dow Global Technologies Inc | Process for preparing soluble polymers with low conversion of acid from aromatic epoxy resins and diacids and process for preparing crosslinked coatings therefrom |
| TW200833729A (en) | 2006-10-10 | 2008-08-16 | Dow Global Technologies Inc | Soluble polymers with low conversion of acids from aromatic epoxy resins and diacids and crosslinked coatings prepared therefrom |
| TW200835708A (en) | 2006-10-10 | 2008-09-01 | Dow Global Technologies Inc | Soluble polymers with high conversion of acid from aromatic epoxy resins and diacids and crosslinked coatings prepared therefrom |
| TW200838893A (en) | 2006-10-10 | 2008-10-01 | Dow Global Technologies Inc | Process for preparing soluble polymers with high conversion of acid from aromatic epoxy resins and diacids and process for preparing crosslinked coatings therefrom |
-
2010
- 2010-11-10 BR BR112012013135A patent/BR112012013135A8/pt not_active IP Right Cessation
- 2010-11-10 WO PCT/US2010/056214 patent/WO2011071650A1/en not_active Ceased
- 2010-11-10 US US13/508,075 patent/US8975343B2/en not_active Expired - Fee Related
- 2010-11-10 KR KR1020127017670A patent/KR20120114296A/ko not_active Withdrawn
- 2010-11-10 CN CN201080055698.7A patent/CN102666636B/zh not_active Expired - Fee Related
- 2010-11-10 EP EP10779628.6A patent/EP2510035B1/en not_active Not-in-force
- 2010-11-10 JP JP2012543125A patent/JP5902625B2/ja not_active Expired - Fee Related
- 2010-12-07 TW TW099142556A patent/TWI503341B/zh not_active IP Right Cessation
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