JP2012140427A5 - - Google Patents
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- JP2012140427A5 JP2012140427A5 JP2011288179A JP2011288179A JP2012140427A5 JP 2012140427 A5 JP2012140427 A5 JP 2012140427A5 JP 2011288179 A JP2011288179 A JP 2011288179A JP 2011288179 A JP2011288179 A JP 2011288179A JP 2012140427 A5 JP2012140427 A5 JP 2012140427A5
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- Prior art keywords
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- catenary
- acrylate
- meth
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- 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.)
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- -1 Carbodiimide compound Chemical class 0.000 claims description 17
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 12
- 239000000178 monomer Substances 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 2
- KCAMXZBMXVIIQN-UHFFFAOYSA-N octan-3-yl 2-methylprop-2-enoate Chemical compound CCCCCC(CC)OC(=O)C(C)=C KCAMXZBMXVIIQN-UHFFFAOYSA-N 0.000 claims description 2
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims 6
- 125000005842 heteroatom Chemical group 0.000 claims 6
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 6
- 125000004432 carbon atom Chemical group C* 0.000 claims 5
- 150000003254 radicals Chemical class 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000004122 cyclic group Chemical group 0.000 claims 3
- 239000003999 initiator Substances 0.000 claims 3
- 125000005647 linker group Chemical group 0.000 claims 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims 2
- 125000005515 organic divalent group Chemical group 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 229920000570 polyether Polymers 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 239000012933 diacyl peroxide Substances 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 150000002432 hydroperoxides Chemical class 0.000 claims 1
- 238000006384 oligomerization reaction Methods 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 238000003672 processing method Methods 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- LAYAKLSFVAPMEL-UHFFFAOYSA-N 1-ethenoxydodecane Chemical compound CCCCCCCCCCCCOC=C LAYAKLSFVAPMEL-UHFFFAOYSA-N 0.000 description 1
- UKDKWYQGLUUPBF-UHFFFAOYSA-N 1-ethenoxyhexadecane Chemical compound CCCCCCCCCCCCCCCCOC=C UKDKWYQGLUUPBF-UHFFFAOYSA-N 0.000 description 1
- QWDQYHPOSSHSAW-UHFFFAOYSA-N 1-isocyanatooctadecane Chemical compound CCCCCCCCCCCCCCCCCCN=C=O QWDQYHPOSSHSAW-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
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- SJIXRGNQPBQWMK-UHFFFAOYSA-N 2-(diethylamino)ethyl 2-methylprop-2-enoate Chemical compound CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 description 1
- SJWKGDGUQTWDRV-UHFFFAOYSA-N 2-Propenyl heptanoate Chemical compound CCCCCCC(=O)OCC=C SJWKGDGUQTWDRV-UHFFFAOYSA-N 0.000 description 1
- SZTBMYHIYNGYIA-UHFFFAOYSA-N 2-chloroacrylic acid Chemical compound OC(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-N 0.000 description 1
- OYUNTGBISCIYPW-UHFFFAOYSA-N 2-chloroprop-2-enenitrile Chemical compound ClC(=C)C#N OYUNTGBISCIYPW-UHFFFAOYSA-N 0.000 description 1
- AEPWOCLBLLCOGZ-UHFFFAOYSA-N 2-cyanoethyl prop-2-enoate Chemical compound C=CC(=O)OCCC#N AEPWOCLBLLCOGZ-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- REEBWSYYNPPSKV-UHFFFAOYSA-N 3-[(4-formylphenoxy)methyl]thiophene-2-carbonitrile Chemical compound C1=CC(C=O)=CC=C1OCC1=C(C#N)SC=C1 REEBWSYYNPPSKV-UHFFFAOYSA-N 0.000 description 1
- QMFVYCZFUFUWDG-UHFFFAOYSA-N 3-phenylbut-3-enenitrile Chemical compound N#CCC(=C)C1=CC=CC=C1 QMFVYCZFUFUWDG-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920001651 Cyanoacrylate Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical class C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Natural products OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical class CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical class CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/982,107 | 2004-11-04 | ||
| US10/982,107 US8440779B2 (en) | 2004-11-04 | 2004-11-04 | Carbodiimide compound and compositions for rendering substrates oil and water repellent |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007540305A Division JP4955565B2 (ja) | 2004-11-04 | 2005-09-21 | カルボジイミド化合物および基材撥油・撥水性付与組成物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012140427A JP2012140427A (ja) | 2012-07-26 |
| JP2012140427A5 true JP2012140427A5 (enExample) | 2014-05-01 |
| JP5654443B2 JP5654443B2 (ja) | 2015-01-14 |
Family
ID=35899851
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007540305A Expired - Lifetime JP4955565B2 (ja) | 2004-11-04 | 2005-09-21 | カルボジイミド化合物および基材撥油・撥水性付与組成物 |
| JP2011288179A Expired - Lifetime JP5654443B2 (ja) | 2004-11-04 | 2011-12-28 | カルボジイミド化合物および基材撥油・撥水性付与組成物 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007540305A Expired - Lifetime JP4955565B2 (ja) | 2004-11-04 | 2005-09-21 | カルボジイミド化合物および基材撥油・撥水性付与組成物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8440779B2 (enExample) |
| EP (2) | EP1807389B1 (enExample) |
| JP (2) | JP4955565B2 (enExample) |
| CN (1) | CN101094831B (enExample) |
| BR (1) | BRPI0517990A (enExample) |
| CA (1) | CA2586108A1 (enExample) |
| WO (1) | WO2006052325A1 (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100984655B1 (ko) * | 2002-03-08 | 2010-10-01 | 사카타 인쿠스 가부시키가이샤 | 처리안료, 그 용도 및 안료처리용 화합물 |
| EP1535971A4 (en) * | 2002-06-25 | 2010-01-20 | Sakata Inx Corp | TREATED PIGMENT, USE THEREOF AND COMPOUND FOR PIGMENT TREATMENT |
| CN1320066C (zh) * | 2002-06-26 | 2007-06-06 | 阪田油墨株式会社 | 颜料分散组合物、其用途以及用于颜料处理的化合物 |
| WO2008154421A1 (en) | 2007-06-08 | 2008-12-18 | 3M Innovative Properties Company | Blends of fluoroalkyl-containing ester oligomers with polydicarbodiimide(s) |
| WO2009036268A2 (en) * | 2007-09-14 | 2009-03-19 | 3M Innovative Properties Company | Composition and method for imparting increased water repellency to substrates and substrates treated with same |
| EP2423186B1 (de) | 2010-08-30 | 2017-05-31 | LANXESS Deutschland GmbH | Neuartige haftvermittler auf basis von carbodiimiden, haftvermittlerhaltige, wässrige resorcin-formaldehyd-latex-dispersionen, haftungsverbesserte fasern, verfahren zu deren herstellung und deren verwendung |
| UA112647C2 (uk) | 2011-05-05 | 2016-10-10 | Басф Се | Інкапсульована частинка |
| BR112017017170B1 (pt) * | 2015-02-13 | 2022-05-10 | 3M Innovative Properties Company | Composição para tratamento isenta de flúor, método para tratamento de um substrato fibroso e substrato fibroso |
| JP6735763B2 (ja) | 2015-02-13 | 2020-08-05 | スリーエム イノベイティブ プロパティズ カンパニー | ポリカルボジイミド及び任意にパラフィンワックスを含むフッ素不含繊維処理組成物、並びに処理方法 |
| JP6987847B2 (ja) * | 2016-08-12 | 2022-01-05 | スリーエム イノベイティブ プロパティズ カンパニー | フッ素非含有繊維処理組成物、処理された基材、及び処理方法 |
| JP7092134B2 (ja) * | 2017-08-15 | 2022-06-28 | 住友ゴム工業株式会社 | 三次元積層造形用ゴム組成物 |
| US20200270478A1 (en) | 2017-09-22 | 2020-08-27 | 3M Innovative Properties Company | Polycarbodiimide-containing compositions, methods, and articles |
| US11015012B2 (en) | 2017-12-27 | 2021-05-25 | 3M Innovative Properties Company | Hydrophobic polyurethane resins |
| US20220325016A1 (en) * | 2019-08-02 | 2022-10-13 | 3M Innovative Properties Company | Acrylate oligomers, acrylate oligomer emulsions, and fluorine-free stain-release compositions containing the same |
| CN111040101B (zh) * | 2019-12-23 | 2021-09-07 | 万华化学集团股份有限公司 | 色值稳定的含有脲二酮基团的多异氰酸酯及其制备方法 |
| US11732083B2 (en) | 2020-11-19 | 2023-08-22 | Covestro Llc | Polyisocyanate resins |
| US20250283273A1 (en) * | 2021-02-03 | 2025-09-11 | 3M Innovative Properties Company | Acrylate oligomers, acrylate oligomer emulsions, and fluorine-free stain-release compositions containing the same |
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| 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 |
| US6737489B2 (en) | 2001-05-21 | 2004-05-18 | 3M Innovative Properties Company | Polymers containing perfluorovinyl ethers and applications for such polymers |
| EP1329548A1 (en) | 2002-01-21 | 2003-07-23 | 3M Innovative Properties Company | Method of treatment of a textile or non-woven substrate to render same water and oil repellent |
| US20040077237A1 (en) | 2002-05-24 | 2004-04-22 | Audenaert Frans A. | Fluorochemical composition comprising perfluoropolyether and an extender for the treatment of fibrous substrates |
| JP4585749B2 (ja) * | 2003-08-07 | 2010-11-24 | 日清紡ホールディングス株式会社 | 黄変を抑えたカルボジイミド組成物、耐加水分解安定剤及び熱可塑性樹脂組成物 |
-
2004
- 2004-11-04 US US10/982,107 patent/US8440779B2/en active Active
-
2005
- 2005-09-21 CA CA002586108A patent/CA2586108A1/en not_active Abandoned
- 2005-09-21 BR BRPI0517990-4A patent/BRPI0517990A/pt not_active Application Discontinuation
- 2005-09-21 JP JP2007540305A patent/JP4955565B2/ja not_active Expired - Lifetime
- 2005-09-21 WO PCT/US2005/033810 patent/WO2006052325A1/en not_active Ceased
- 2005-09-21 EP EP05799776.9A patent/EP1807389B1/en not_active Expired - Lifetime
- 2005-09-21 EP EP17161978.6A patent/EP3210968A1/en not_active Withdrawn
- 2005-09-21 CN CN200580045893.0A patent/CN101094831B/zh not_active Expired - Lifetime
-
2011
- 2011-12-28 JP JP2011288179A patent/JP5654443B2/ja not_active Expired - Lifetime
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