JP2015531423A5 - - Google Patents
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- Publication number
- JP2015531423A5 JP2015531423A5 JP2015535778A JP2015535778A JP2015531423A5 JP 2015531423 A5 JP2015531423 A5 JP 2015531423A5 JP 2015535778 A JP2015535778 A JP 2015535778A JP 2015535778 A JP2015535778 A JP 2015535778A JP 2015531423 A5 JP2015531423 A5 JP 2015531423A5
- Authority
- JP
- Japan
- Prior art keywords
- carbodiimide
- prepolymer
- oxide
- isocyanate
- aliphatic
- 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
- 150000001718 carbodiimides Chemical class 0.000 claims description 18
- 239000012948 isocyanate Substances 0.000 claims description 13
- 150000002513 isocyanates Chemical class 0.000 claims description 13
- 229920005862 polyol Polymers 0.000 claims description 13
- -1 aliphatic polyol Chemical class 0.000 claims description 11
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 150000003077 polyols Chemical class 0.000 claims description 6
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 5
- 229920000570 polyether Polymers 0.000 claims description 5
- VPKDCDLSJZCGKE-UHFFFAOYSA-N carbodiimide group Chemical group N=C=N VPKDCDLSJZCGKE-UHFFFAOYSA-N 0.000 claims description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims 2
- 239000011342 resin composition Substances 0.000 claims 2
- 150000007942 carboxylates Chemical class 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 19
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 235000011056 potassium acetate Nutrition 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 5
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 5
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 150000003138 primary alcohols Chemical class 0.000 description 2
- IFZAHHXECWEMAO-UHFFFAOYSA-N 1-(3-methylphenyl)-2,3-dihydro-1$l^{5}-phosphole 1-oxide Chemical group CC1=CC=CC(P2(=O)C=CCC2)=C1 IFZAHHXECWEMAO-UHFFFAOYSA-N 0.000 description 1
- YUQUHJGNZFFDAA-UHFFFAOYSA-N 1-phenyl-2,3-dihydro-1$l^{5}-phosphole 1-oxide Chemical compound C=1C=CC=CC=1P1(=O)CCC=C1 YUQUHJGNZFFDAA-UHFFFAOYSA-N 0.000 description 1
- YMKWWHFRGALXLE-UHFFFAOYSA-N 4-methyl-1-phenyl-2,3-dihydro-1$l^{5}-phosphole 1-oxide Chemical compound C1CC(C)=CP1(=O)C1=CC=CC=C1 YMKWWHFRGALXLE-UHFFFAOYSA-N 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- SAJCVFNJOGNICP-UHFFFAOYSA-N C(C)P1(CC(=CC=C1)C)=O Chemical compound C(C)P1(CC(=CC=C1)C)=O SAJCVFNJOGNICP-UHFFFAOYSA-N 0.000 description 1
- MRBNJAMYAHSBFS-UHFFFAOYSA-N C1(=CC=CC=C1)P1(CC(=CC=C1)C)=O Chemical compound C1(=CC=CC=C1)P1(CC(=CC=C1)C)=O MRBNJAMYAHSBFS-UHFFFAOYSA-N 0.000 description 1
- IPCUUURCYULXHA-UHFFFAOYSA-N CP1(CC(=CC=C1)C)=O Chemical compound CP1(CC(=CC=C1)C)=O IPCUUURCYULXHA-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- ZBVOEVQTNYNNMY-UHFFFAOYSA-N O=P1=CCCC1 Chemical class O=P1=CCCC1 ZBVOEVQTNYNNMY-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229940117927 ethylene oxide Drugs 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- QJMMCGKXBZVAEI-UHFFFAOYSA-N tris(trimethylsilyl) phosphate Chemical compound C[Si](C)(C)OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C QJMMCGKXBZVAEI-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261710791P | 2012-10-08 | 2012-10-08 | |
| US61/710,791 | 2012-10-08 | ||
| PCT/US2013/063204 WO2014058700A1 (en) | 2012-10-08 | 2013-10-03 | Curing of aromatic carbodiimides |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015531423A JP2015531423A (ja) | 2015-11-02 |
| JP2015531423A5 true JP2015531423A5 (enExample) | 2017-11-30 |
| JP6309958B2 JP6309958B2 (ja) | 2018-04-11 |
Family
ID=49356534
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015535778A Active JP6309958B2 (ja) | 2012-10-08 | 2013-10-03 | 芳香族カルボジイミドの硬化 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US9328189B2 (enExample) |
| EP (1) | EP2885351B1 (enExample) |
| JP (1) | JP6309958B2 (enExample) |
| CN (1) | CN104704056B (enExample) |
| BR (1) | BR112015006952B1 (enExample) |
| MX (1) | MX2015003858A (enExample) |
| RU (1) | RU2642462C2 (enExample) |
| TW (1) | TWI500701B (enExample) |
| WO (1) | WO2014058700A1 (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019027631A1 (en) * | 2017-07-31 | 2019-02-07 | Dow Global Technologies Llc | DETERGENT ADDITIVE |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE530008A (enExample) | 1953-06-30 | |||
| US2800457A (en) | 1953-06-30 | 1957-07-23 | Ncr Co | Oil-containing microscopic capsules and method of making them |
| JPS56140354A (en) | 1980-04-04 | 1981-11-02 | Hitachi Ltd | Manufacture of composite type electrophotographic plate |
| JPS6140354A (ja) * | 1984-08-01 | 1986-02-26 | Teijin Ltd | 樹脂組成物 |
| JPS61268714A (ja) * | 1985-05-22 | 1986-11-28 | Nisshinbo Ind Inc | 耐熱性の高い熱硬化性樹脂の製造方法 |
| DE3643238C2 (enExample) * | 1985-03-29 | 1989-08-03 | Nisshinbo Industries, Inc., Tokio/Tokyo, Jp | |
| US5271881A (en) | 1987-09-28 | 1993-12-21 | Redding Bruce K | Apparatus and method for making microcapsules |
| IT1230705B (it) * | 1989-01-27 | 1991-10-29 | Boston Spa | Composizione di hot melt reticolabile |
| JPH05320611A (ja) * | 1992-05-18 | 1993-12-03 | Nisshinbo Ind Inc | フィルム状接着剤組成物 |
| US5574083A (en) * | 1993-06-11 | 1996-11-12 | Rohm And Haas Company | Aromatic polycarbodiimide crosslinkers |
| US5357021A (en) | 1993-07-21 | 1994-10-18 | Basf Corporation | Reactive carbodimide compositions |
| JP2002187932A (ja) * | 2000-12-19 | 2002-07-05 | Dainichiseika Color & Chem Mfg Co Ltd | ポリカルボジイミド化合物、その製造方法および物品の処理方法 |
| DE602005008661D1 (de) * | 2004-05-03 | 2008-09-18 | Rohm & Haas | Michael-addierungs Zusammensetzungen |
| EP1593728B1 (en) | 2004-05-03 | 2012-05-09 | Rohm And Haas Company | Michael addition compositions |
| EP1640388B1 (en) * | 2004-09-24 | 2015-02-25 | Rohm and Haas Company | Biomass based Michael addition composition |
| DE502008000184D1 (de) * | 2007-03-05 | 2009-12-31 | Basf Se | Kompaktes Polyisocyanurat mit verbesserten Verarbeitungs-und Produkteigenschaften sowie verfahren zu seiner Herstellung |
-
2013
- 2013-09-16 TW TW102133455A patent/TWI500701B/zh active
- 2013-10-03 RU RU2015117392A patent/RU2642462C2/ru active
- 2013-10-03 CN CN201380052343.6A patent/CN104704056B/zh active Active
- 2013-10-03 EP EP13776924.6A patent/EP2885351B1/en active Active
- 2013-10-03 BR BR112015006952-5A patent/BR112015006952B1/pt active IP Right Grant
- 2013-10-03 WO PCT/US2013/063204 patent/WO2014058700A1/en not_active Ceased
- 2013-10-03 US US14/431,811 patent/US9328189B2/en active Active
- 2013-10-03 JP JP2015535778A patent/JP6309958B2/ja active Active
- 2013-10-03 MX MX2015003858A patent/MX2015003858A/es active IP Right Grant
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