JP2005511874A5 - - Google Patents
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- JP2005511874A5 JP2005511874A5 JP2003552829A JP2003552829A JP2005511874A5 JP 2005511874 A5 JP2005511874 A5 JP 2005511874A5 JP 2003552829 A JP2003552829 A JP 2003552829A JP 2003552829 A JP2003552829 A JP 2003552829A JP 2005511874 A5 JP2005511874 A5 JP 2005511874A5
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- 239000000203 mixture Substances 0.000 claims 15
- 150000001875 compounds Chemical class 0.000 claims 11
- -1 heteroacyloxy Chemical group 0.000 claims 7
- 125000001931 aliphatic group Chemical group 0.000 claims 6
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims 6
- 239000000126 substance Substances 0.000 claims 4
- 125000002723 alicyclic group Chemical group 0.000 claims 3
- 125000002947 alkylene group Chemical group 0.000 claims 3
- 125000004474 heteroalkylene group Chemical group 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 229920001228 Polyisocyanate Polymers 0.000 claims 2
- 239000007795 chemical reaction product Substances 0.000 claims 2
- 239000008199 coating composition Substances 0.000 claims 2
- 125000004185 ester group Chemical group 0.000 claims 2
- 239000000835 fiber Substances 0.000 claims 2
- 150000002513 isocyanates Chemical class 0.000 claims 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 2
- 239000005056 polyisocyanate Substances 0.000 claims 2
- 239000000758 substrate Substances 0.000 claims 2
- 125000004423 acyloxy group Chemical group 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 239000002981 blocking agent Substances 0.000 claims 1
- 125000004432 carbon atoms Chemical group C* 0.000 claims 1
- 125000005392 carboxamide group Chemical group NC(=O)* 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 125000002993 cycloalkylene group Chemical group 0.000 claims 1
- 125000001475 halogen functional group Chemical group 0.000 claims 1
- 125000004405 heteroalkoxy group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000005647 linker group Chemical group 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 150000002923 oximes Chemical group 0.000 claims 1
- 229910000077 silane Inorganic materials 0.000 claims 1
- 150000004756 silanes Chemical class 0.000 claims 1
- 239000002689 soil Substances 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 125000000565 sulfonamide group Chemical group 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- 150000003673 urethanes Chemical class 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Claims (14)
- (a)(1)1種または複数種の多官能性イソシアネート化合物;
(2)1種または複数種の親水性ポリオキシアルキレン化合物;
(3)次式:
X−R1−Si−(Y)3
(式中、Xは、−NH2;−SH;−OH;−N=C=O;または−NRH(Rは、フェニル、直鎖および分枝鎖の脂肪族、脂環式、および脂肪族エステル基からなる群から選択される)であり;R1は、アルキレン、ヘテロアルキレン、アラルキレン、またはヘテロアラルキレン基であり;
各Yはそれぞれ独立して、ヒドロキシル;アルコキシ、アシルオキシ、ヘテロアルコキシ、ヘテロアシルオキシ、ハロ、およびオキシムからなる群から選択される加水分解性部位;またはフェニル、脂環式、直鎖脂肪族、および分枝鎖脂肪族からなる群から選択される非加水分解性部位であり、少なくとも1つのYは加水分解性部位である)の1種または複数種のシラン化合物;および
(4)次式:
R f −Z−R 2 −X
{式中、R f は、パーフルオロアルキル基またはパーフルオロへテロアルキル基であり;
Zは、共有結合、スルホンアミド基、カルボキサミド基、カルボキシル基、またはスルホニル基から選択される連結基であり;
R 2 は、炭素原子1〜14個の、直鎖または分枝鎖の二価アルキレン、シクロアルキレン、またはヘテロアルキレン基であり;
Xは、−NH 2 ;−SH;−OH;−N=C=O;または−NRH(Rは、フェニル、直鎖および分枝鎖の脂肪族、脂環式、および脂肪族エステル基からなる群から選択される)であり;R 1 は、アルキレン、ヘテロアルキレン、アラルキレン、またはヘテロアラルキレン基である。}
の1種または複数種のフルオロケミカル単官能性化合物;
の反応生成物を含む1種または複数種のウレタンを含む第1成分と、
(b)前記フルオロケミカルウレタン化合物で処理される繊維基材の撥油性および/または撥水性あるいはソイル/ステインリリース性をさらに改善することができる、1種または複数種の親水性補助化合物を含む第2成分と、
を含有する化学組成物。 - Rfが、炭素2〜12個のパーフルオロアルキル基である、請求項1に記載の化学組成物。
- 前記第2補助成分が、ポリイソシアネート、ブロック剤、ポリオキシアルキレン化合物の反応生成物である、請求項1に記載の組成物。
- 前記第2成分のポリイソシアネートの前記イソシアネート基が、ブロックイソシアネート基である、請求項3に記載の組成物。
- 前記第1成分の前記親水性ポリオキシアルキレン化合物の量が、前記ウレタン化合物の利用可能なイソシアネート基の0.1〜30%と反応するのに十分な量であり、前記シラン化合物の量が、前記ウレタン化合物の利用可能なイソシアネート基の0.1〜25%と反応するのに十分な量であり、かつ前記フルオロケミカル単官能性化合物の量が、前記ウレタン化合物の利用可能なイソシアネート基の60〜90%と反応するのに十分な量である、請求項1に記載の組成物。
- 前記第2成分の前記ポリオキシアルキレン化合物の量が、前記補助化合物の利用可能なイソシアネート基の約25〜約75%が反応するような量である、請求項3に記載の組成物。
- 前記第1成分のウレタン化合物と前記第2補助化合物との比が、12:1〜1:12である、請求項1に記載の組成物。
- 前記第1成分の前記ポリオキシアルキレン化合物が、1を超える官能価を有する、請求項1に記載の組成物。
- 前記第2成分の前記ポリオキシアルキレン化合物が、1の官能価を有する、請求項3に記載の組成物。
- 請求項1〜9のいずれか一項に記載の化学組成物と溶媒との溶液を含む、処理用組成物。
- 化学組成物を約0.1〜約50%含有する、請求項10に記載の処理用組成物。
- 請求項10に記載の処理用組成物から得られる硬化されたコーティングを有する繊維基材を含む物品。
- 請求項10に記載の処理用組成物を塗布する段階と、そのコーティング組成物を硬化させる段階と、を含む繊維基材にステインリリース特性を付与する方法。
- 前記コーティング組成物が、繊維上に固体0.05%〜5%を提供するのに十分な量で塗布される、請求項13に記載の方法。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/022,118 US6890360B2 (en) | 2001-12-17 | 2001-12-17 | Fluorochemical urethane composition for treatment of fibrous substrates |
PCT/US2002/033781 WO2003051953A1 (en) | 2001-12-17 | 2002-10-22 | Fluorochemical urethane composition for treatment of fibrous substrates |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2005511874A JP2005511874A (ja) | 2005-04-28 |
JP2005511874A5 true JP2005511874A5 (ja) | 2006-01-05 |
Family
ID=21807901
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2003552829A Pending JP2005511874A (ja) | 2001-12-17 | 2002-10-22 | 繊維基材の処理に用いられるフルオロケミカルウレタン組成物 |
Country Status (9)
Country | Link |
---|---|
US (1) | US6890360B2 (ja) |
EP (1) | EP1458782B1 (ja) |
JP (1) | JP2005511874A (ja) |
KR (1) | KR20040068260A (ja) |
CN (1) | CN100406486C (ja) |
AT (1) | ATE493453T1 (ja) |
AU (1) | AU2002342090A1 (ja) |
DE (1) | DE60238787D1 (ja) |
WO (1) | WO2003051953A1 (ja) |
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US20060013983A1 (en) * | 2004-07-15 | 2006-01-19 | 3M Innovative Properties Company | Adhesive delivery of oil and water repellents |
US7345123B2 (en) * | 2004-12-28 | 2008-03-18 | 3M Innovative Properties Company | Fluoroacrylate-multifunctional acrylate copolymer compositions |
US7253241B2 (en) * | 2004-12-28 | 2007-08-07 | 3M Innovative Properties Company | Fluorochemical containing low adhesion backsize |
US20060142530A1 (en) | 2004-12-28 | 2006-06-29 | Moore George G | Water- and oil-repellent fluorourethanes and fluoroureas |
US7291688B2 (en) * | 2004-12-28 | 2007-11-06 | 3M Innovative Properties Company | Fluoroacrylate-mercaptofunctional copolymers |
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US20070014927A1 (en) * | 2005-07-15 | 2007-01-18 | Buckanin Richard S | Fluorochemical urethane composition for treatment of fibrous substrates |
US7494511B2 (en) * | 2006-05-08 | 2009-02-24 | E.I. Du Pont De Nemours And Company | Hydrophilic stain release agents |
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US20080116414A1 (en) * | 2006-11-22 | 2008-05-22 | 3M Innovative Properties Company | Fluorochemical composition for treatment of a fibrous substrate |
US7964552B2 (en) | 2006-12-15 | 2011-06-21 | E. I. Du Pont De Nemours And Company | Fluorosurfactant with disproportionate effect |
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WO2008077029A1 (en) * | 2006-12-18 | 2008-06-26 | 3M Innovative Properties Company | Extenders for fluorochemical treatment of fibrous substrates |
US7723414B2 (en) | 2006-12-22 | 2010-05-25 | E. I. Du Pont De Nemours And Company | Antistatic system for polymers |
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CN102282191A (zh) * | 2008-11-25 | 2011-12-14 | 3M创新有限公司 | 氟化醚尿烷及其使用方法 |
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US8544987B2 (en) * | 2010-08-20 | 2013-10-01 | Xerox Corporation | Thermally stable oleophobic low adhesion coating for inkjet printhead front face |
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KR20200088915A (ko) | 2017-12-13 | 2020-07-23 | 도날드슨 컴파니, 인코포레이티드 | 소유성 폴리아미드 미세 섬유, 방법, 필터 매체, 및 필터 요소 |
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-
2001
- 2001-12-17 US US10/022,118 patent/US6890360B2/en not_active Expired - Lifetime
-
2002
- 2002-10-22 AU AU2002342090A patent/AU2002342090A1/en not_active Abandoned
- 2002-10-22 WO PCT/US2002/033781 patent/WO2003051953A1/en active Application Filing
- 2002-10-22 DE DE60238787T patent/DE60238787D1/de not_active Expired - Lifetime
- 2002-10-22 KR KR10-2004-7009408A patent/KR20040068260A/ko not_active Application Discontinuation
- 2002-10-22 JP JP2003552829A patent/JP2005511874A/ja active Pending
- 2002-10-22 AT AT02776256T patent/ATE493453T1/de not_active IP Right Cessation
- 2002-10-22 EP EP20020776256 patent/EP1458782B1/en not_active Expired - Lifetime
- 2002-10-22 CN CNB02825175XA patent/CN100406486C/zh not_active Expired - Fee Related
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