JP2008533320A5 - - Google Patents

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JP2008533320A5
JP2008533320A5 JP2008501294A JP2008501294A JP2008533320A5 JP 2008533320 A5 JP2008533320 A5 JP 2008533320A5 JP 2008501294 A JP2008501294 A JP 2008501294A JP 2008501294 A JP2008501294 A JP 2008501294A JP 2008533320 A5 JP2008533320 A5 JP 2008533320A5
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halogen
phenyl group
substituted
dyed
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Priority claimed from PCT/EP2006/060718 external-priority patent/WO2006097475A1/en
Publication of JP2008533320A publication Critical patent/JP2008533320A/en
Publication of JP2008533320A5 publication Critical patent/JP2008533320A5/ja
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Claims (10)

分散染料を用いた、熱力学的に相溶するポリオレフィン及びポリアミドから構成される複数成分系繊維上の染色物の耐光堅牢度を向上させる方法であって、
当該複数成分系繊維が、ベンゾトリアゾール誘導体を用いて処理されることを特徴とする方法。 A method for improving the light fastness of a dyed product on a multi-component fiber composed of a thermodynamically compatible polyolefin and polyamide using a disperse dye,
A method wherein the multicomponent fiber is treated with a benzotriazole derivative. 前記ベンゾトリアゾール誘導体が、次の式（Ｉ）：
Figure 2008533320
 （式中、
Ｒ1はハロゲン原子であり、
Ｒ2はＣ1〜Ｃ6のアルキルであり、そして
Ｒ3はＣ1〜Ｃ6のアルキルである）
のベンゾトリアゾール誘導体であることを特徴とする、請求項１に記載の方法。 Said benzotriazole derivative has the following formula (I):
Figure 2008533320
 (Where
R 1 is a halogen atom;
R 2 is C 1 -C 6 alkyl and R 3 is C 1 -C 6 alkyl)
The method according to claim 1, which is a benzotriazole derivative. 前記複数成分系繊維が、ポリプロピレン、変性されたＰＡ及びポリアミドから成ることを特徴とする、請求項１又は２に記載の方法。 The multicomponent fibers, characterized in that consisting of polypropylene, modified PA and polyamide, the method according to claim 1 or 2. 前記複数成分系繊維が第一のポリマーのコアから成ることと、当該コアが第二のポリマーにより覆われていることとを特徴とする、請求項１〜３のいずれか一項に記載の方法。 And said plurality bicomponent fiber consists of a core of a first polymer, and characterized in that said core is covered by the second polymer, the method according to any one of claims 1 to 3 . 前記ベンゾトリアゾール誘導体が、乾燥重量に基づいて、０．０１〜２０重量％の量で用いられる、請求項１〜４のいずれか一項に記載の方法。 The method according to any one of claims 1 to 4, wherein the benzotriazole derivative is used in an amount of 0.01 to 20% by weight, based on dry weight. 前記分散染料が、次の式（１）：
Figure 2008533320
 （式中、Ｒ4及びＲ’4は、独立して、フェニル基、又はハロゲン、−ＣＨ3、−ＣＨ2ＣＨ3、−ＯＣＨ3、−ＯＣＨ2ＣＨ3若しくは−ＯＨにより置換されたフェニル基である）、
又は次の式（２）、式（３）若しくは式（４）：
Figure 2008533320
 （式中、Ｒ5、Ｒ’5、及びＲ”5は、独立して、ハロゲン、フェニル基、又はハロゲン、−ＣＨ3、−ＣＨ2ＣＨ3、−ＯＣＨ3、−ＯＣＨ2ＣＨ3若しくは−ＯＨにより置換されたフェニル基である）、
又は次の式（５）：
Figure 2008533320
 （式中、
Ｒ6は、ハロゲン、フェニル基、若しくはハロゲン、−ＣＨ3、−ＣＨ2ＣＨ3、−ＯＣＨ3、−ＯＣＨ2ＣＨ3若しくは−ＯＨにより置換されたフェニル基、又はフェノキシ基、若しくはハロゲン、−ＣＨ3、−ＣＨ2ＣＨ3、−ＯＣＨ3、−ＯＣＨ2ＣＨ3若しくは−ＯＨにより置換されたフェノキシ基であり、
Ｒ7は、フェニル基、又はハロゲン、−ＣＨ3、−ＣＨ2ＣＨ3、−ＯＣＨ3、−ＯＣＨ2ＣＨ3若しくは−ＯＨにより置換されたフェニル基であり、
Ｒ8は、−ＮＨ2又は−ＮＨＲ9であり、ここでＲ9は、ハロゲン、フェニル基、若しくはハロゲン、−ＣＨ3、−ＣＨ2ＣＨ3、−ＯＣＨ3、−ＯＣＨ2ＣＨ3若しくは−ＯＨにより置換されたフェニル基、又はフェノキシ基、若しくはハロゲン、−ＣＨ3、−ＣＨ2ＣＨ3、−ＯＣＨ3、−ＯＣＨ2ＣＨ3若しくは−ＯＨにより置換されたフェノキシ基であるか、あるいはＲ9は、式ＳＯ2−フェニルの基であり、ここで当該ＳＯ2−フェニル基のフェニル基は、置換されていないか、又はハロゲン、−ＣＨ3、−ＣＨ2ＣＨ3、−ＯＣＨ3、−ＯＣＨ2ＣＨ3若しくは−ＯＨにより置換されたフェニル基であるか、又はハロゲン、−ＣＨ3、−ＣＨ2ＣＨ3、−ＯＣＨ3、−ＯＣＨ2ＣＨ3若しくは−ＯＨにより置換されたフェノキシ基である）
又は次の式（６）：
Figure 2008533320
 （式中、Ｒ10は、Ｈ又はハロゲンである）
を有することを特徴とする、請求項１〜５のいずれか一項に記載の方法。 The disperse dye is represented by the following formula (1):
Figure 2008533320
 (Wherein, R 4 and R '4 are independently a phenyl group, or a halogen, -CH 3, -CH 2 CH 3 , -OCH 3, substituted by -OCH 2 CH 3 or -OH phenyl Group),
Or the following formula (2), formula (3) or formula (4):
Figure 2008533320
 (Wherein, R 5, R '5, and R "5 are independently halogen, phenyl group, or a halogen, -CH 3, -CH 2 CH 3 , -OCH 3, -OCH 2 CH 3 Or a phenyl group substituted by —OH),
Or the following formula (5):
Figure 2008533320
 (Where
R 6 is halogen, phenyl group, or a halogen, -CH 3, -CH 2 CH 3 , -OCH 3, phenyl substituted by -OCH 2 CH 3 or -OH, or Fe phenoxy group, or a halogen emissions, -CH 3, -CH 2 CH 3 , -OCH 3, phenoxy group substituted by -OCH 2 CH 3 or -OH,
R 7 is phenyl group, or a halogen, -CH 3, -CH 2 CH 3 , -OCH 3, a phenyl group substituted by -OCH 2 CH 3 or -OH,
R 8 is -NH 2 or -NHR 9, wherein R 9 is halogen, phenyl group, or a halogen, -CH 3, -CH 2 CH 3 , -OCH 3, -OCH 2 CH 3 or phenyl group substituted by -OH, or Fe phenoxy group, or a halogen, -CH 3, -CH 2 CH 3 , -OCH 3, or a phenoxy group substituted by -OCH 2 CH 3 or -OH, or R 9 has the formula SO 2 - is a radical of the phenyl, wherein said SO 2 - phenyl group of the phenyl group is unsubstituted or substituted with or halogen, -CH 3, -CH 2 CH 3 , -OCH 3, or a phenyl group substituted by -OCH 2 CH 3 or -OH, or halogen, -CH 3, -CH 2 CH 3, -OCH 3, substituted by -OCH 2 CH 3 or -OH in Fe phenoxy group is there)
Or the following equation (6):
Figure 2008533320
 (Wherein, R 10 is H or halogen)
The method according to any one of claims 1 to 5 , characterized by comprising: 分散染料を用いて染色された、熱力学的に相溶するポリオレフィン及びポリアミドから構成される耐光堅牢性を有する染色をされた複数成分系繊維であって、ベンゾトリアゾール誘導体を用いて処理されたことを特徴とする複数成分系繊維。   Light-fast dyed multicomponent fibers composed of thermodynamically compatible polyolefins and polyamides dyed with disperse dyes, treated with benzotriazole derivatives A multi-component fiber characterized by カーペット及び／又はテキスタイル製床敷物を製造するための、請求項７に記載の耐光堅牢性を有する染色をされた複数成分系繊維の使用。   Use of a dyed multicomponent fiber according to claim 7 for the production of carpet and / or textile floor coverings. 熱力学的に相溶するポリオレフィン及びポリアミドから構成される複数成分系繊維を処理するためのベンゾトリアゾール誘導体の使用。   Use of benzotriazole derivatives to treat multicomponent fibers composed of thermodynamically compatible polyolefins and polyamides. 熱力学的に相溶するポリオレフィン及びポリアミドから構成される、染色された複数成分系繊維の耐光堅牢度を向上させるための、請求項９に記載のベンゾトリアゾール誘導体の使用。 Consists thermodynamically compatible to polyolefins and polyamides, for improving the light fastness of dyed multicomponent fibers, the use of benzotriazole derivatives according to claim 9.
JP2008501294A 2005-03-18 2006-03-14 Dyeing with light fastness on bicomponent fiber Pending JP2008533320A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP05102203 2005-03-18
PCT/EP2006/060718 WO2006097475A1 (en) 2005-03-18 2006-03-14 Light-fast dyeings on bicomponent fibres

Publications (2)

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JP2008533320A JP2008533320A (en) 2008-08-21
JP2008533320A5 true JP2008533320A5 (en) 2009-03-12

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US (1) US20090025151A1 (en)
EP (1) EP1863973B1 (en)
JP (1) JP2008533320A (en)
CN (1) CN101142358B (en)
BR (1) BRPI0608449A2 (en)
ES (1) ES2364184T3 (en)
PT (1) PT1863973E (en)
TW (1) TWI402395B (en)
WO (1) WO2006097475A1 (en)

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DE102006020661A1 (en) * 2006-05-04 2007-11-22 TAG Textilausrüstungs-Gesellschaft Schroers GmbH & Co KG Modern multi-component clean fiber e.g. methotrexate fiber, coloring method, for e.g. carpet goods, involves maintaining cross section of fiber and fibrils with coat of additives, where fibrils are embedded in fiber
JP2009030214A (en) * 2007-07-27 2009-02-12 Senka Kk Light fastness improver for fiber product, and method for improving light fastness
CN101974250B (en) * 2010-07-30 2013-04-24 江苏亚邦染料股份有限公司 Yellow disperse dye with high light fastness
KR101596065B1 (en) * 2011-04-08 2016-02-29 코오롱인더스트리 주식회사 Composition for Aramid and Aramid Product Manufactured Using The Same
US10058808B2 (en) 2012-10-22 2018-08-28 Cummins Filtration Ip, Inc. Composite filter media utilizing bicomponent fibers

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JPS59216979A (en) * 1983-05-18 1984-12-07 三洋化成工業株式会社 Treating agent for fiber
EP0354174A1 (en) * 1988-07-01 1990-02-07 Ciba-Geigy Ag Stable aqueous composition for modifying light fastness
EP0409771A3 (en) * 1989-06-27 1991-06-12 Ciba-Geigy Ag Process of photochemical and thermal stabilization of polyamide fibres, dyeable by acid and basic dyes, and of their mixtures amongst themselves and with other fibres
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ES2128024T3 (en) * 1994-09-30 1999-05-01 Ciba Geigy Ag STABILIZATION OF PIGMENTED FIBER WITH A SYNERGISTIC BLEND OF PREVIOUS AMINE AND UV ABSORBER.
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