| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | 耐光性能优良超纤合成革及其制备方法 | CN201710733346.6 | 2017-08-24 | CN107447293A | 2017-12-08 | 胡忠杰; 韩芹; 张其斌; 杜明兵; 孙向浩 |
| 本发明公开了一种耐光性能优良超纤合成革及其制备方法，制备方法，包括如下步骤：(1)将尼龙6、低密度聚乙烯、二氧化钛消光尼龙6混合和相容剂混合，制备获得不定岛海岛短纤维，组分的重量份数为：尼龙6100份，二氧化钛消光尼龙6 1～10份，低密度聚乙烯80～100份，相容剂1～5份，(2)然后将所述的不定岛海岛短纤维，进行纺丝、制备成为无纺布，并依次进行浸渍、减量、烘干上油、揉皮、片皮、磨皮、染色、水洗、烘干和后整理，获得耐光性能优良的超纤革，所述的相容剂为发泡热塑性聚氨酯弹性体。采用上述方法获得的染色超纤革，光照牢度高，解决了染色超纤革的耐光照牢度问题。 | ||||||
| 2 | 一种裘皮用新型环保酸性蓝色染料及合成方法 | CN201710607177.1 | 2017-07-24 | CN107345080A | 2017-11-14 | 陶钧峰; 郑超斌; 郑红超 |
| 本发明提供了一种裘皮用新型环保酸性蓝色染料及合成方法，本申请所提供的裘皮用新型环保酸性蓝色染料，分子式为C22H17N2SO6Na，该染料为蒽醌类酸性染料，分子质量为460，比较小，非常适合裘皮染色。分子结构具有很好的直线性，所以该染料有很好的配伍性能。具有上色率高、吸净率高、配伍性好、色泽饱满一系列优点。不含有欧盟禁用的24种芳香烃，是一支环保型染料，该染料无致敏性，具有安全性。该裘皮用新型环保酸性蓝色染料的合成方法，经过缩合反应和烘干两个步骤，具有方便、简单、易于合成等优点。 | ||||||
| 3 | 用于聚酰胺和羊毛的酸性染料混合物 | CN201280029398.0 | 2012-06-13 | CN103619961A | 2014-03-05 | H·希波尔; R·努瑟; R·马拉兹 |
| 本发明涉及一种酸性染料混合物，其包含a)20至95重量%的至少一种具有通式结构(A)的染料A，和b)5至80重量%的至少一种具有通式结构(B)的染料B。 | ||||||
| 4 | 一种毛革黑酸性染料及其制备方法 | CN201710607780.X | 2017-07-24 | CN107312359A | 2017-11-03 | 王亮; 郑超斌; 郑红超; 康定国 |
| 本发明提供了一种毛革黑酸性染料，主要由以下原料制得：按质量份数计，染料80-95份，丙烯酰胺与丙烯酸的二元共聚物2-10份。还提供了该毛革黑酸性染料的制备方法，包括如下步骤：将所有原料在10-50℃下混合搅拌均匀，即得。本发明实施例提供的毛革酸性染料通过原料之间互相组配之后达到增深、固色的效果，其中，丙烯酰胺与丙烯酸的二元共聚物与染料中的磺酸基结合有效降低了染料中的水溶性基团量，从而提高了染料本身的稳定性，另外应用也比较方便，填补了相关技术空白，值得广泛推广应用。 | ||||||
| 5 | 新型化合物、染色或印花用着色组合物、喷墨用油墨、布帛印花方法及被染色或印花布帛 | CN201580034526.4 | 2015-07-03 | CN106661337A | 2017-05-10 | 八木一成; 小林博美; 饭泉隆史; 永田美彰; 立石桂一; 古川和史 |
| 本发明通过以说明书中记载的通式(1)～(3)的任一个表示的化合物，例如下述化合物及包含该化合物的染色或印花用着色组合物、含有上述染色或印花用着色组合物的喷墨用油墨、对布帛进行印花的方法及被染色或印花的布帛，提供一种色调优异、成色浓度较高、耐光性、耐水性及耐氯性优异的化合物及包含该化合物的染色或印花用着色组合物、含有上述染色或印花用着色组合物的喷墨用油墨、对布帛进行印花的方法及被染色或印花的布帛。 | ||||||
| 6 | 一种赤藓红对相变调温粘胶纤维的染色方法 | CN201510915998.2 | 2015-12-10 | CN105401466A | 2016-03-16 | 刘艳春; 金美菊; 白刚 |
| 本发明公开了一种赤藓红对相变调温粘胶纤维的染色方法，其特征在于：利用阳离子醚化剂对相变调温粘胶纤维进行预处理，使处理后的相变调温粘胶纤维表面呈阳荷性，对色素的吸附能力大大增强，对色素负离子有静电吸引力，增加了赤藓红上染相变调温粘胶纤维的染座，从而大大提高了上染百分率和色牢度。实现了既生态环保、又有较高得色率的赤藓红色素在相变调温粘胶纤维上的染色。 | ||||||
| 7 | NOVEL COMPOUND, COLORING COMPOSITION FOR DYEING OR TEXTILE PRINTING, INK JET INK, METHOD OF PRINTING ON FABRIC, AND DYED OR PRINTED FABRIC | US15384497 | 2016-12-20 | US20170101533A1 | 2017-04-13 | Kazunari YAGI; Hiromi KOBAYASHI; Takashi IIZUMI; Yoshiaki NAGATA; Keiichi TATEISHI; Kazushi FURUKAWA |
| Provided are a compound represented by any one of Formulae (1) to (3) (for example, the following compound), a coloring composition for dyeing or textile printing including the compound, an ink jet ink including the coloring composition for dyeing or textile printing, a method of printing on fabric, and a dyed or printed fabric, in which the color is excellent, the color optical density is high, and light fastness, water fastness, and chlorine fastness are excellent. | ||||||
| 8 | Method for printing fibrous textile materials using the ink jet technique | US09720958 | 2001-01-03 | US06511535B1 | 2003-01-28 | Roger Lacroix; Peter Scheibli; Mickael Mheidle |
| The invention relates to a method for printing fibrous textile materials using the ink-jet printing technique, wherein the fibrous materials are printed with an aqueous ink that comprises at least one acid dye according to claim 1 and that has a viscosity of from 1 to 40 mPa·s. | ||||||
| 9 | Anthraquinone compounds and process for dyeing therewith | US191077 | 1980-09-26 | US4330294A | 1982-05-18 | Roland Wald |
| The present invention relates to compounds of formula ##STR1## in which R.sub.1 is an aliphatic or alicyclic hydrocarbon radical,R.sub.2 is hydrogen, halogen or C.sub.1-8 alkyl,M is hydrogen or an equivalent of a non-chromophoric cationand mixtures of such compounds with the corresponding ethers, which mixtures are useful as anionic dyestuffs. | ||||||
| 10 | COLORING COMPOSITION FOR DYEING, COLORING COMPOSITION FOR PRINTING, PRINTING METHOD, INKJET PRINTING INK, AND DYED FABRIC | EP15863010 | 2015-11-19 | EP3225663A4 | 2017-10-04 | YAGI KAZUNARI; TATEISHI KEIICHI; IIZUMI TAKASHI; HAKAMATA AKIHIRO; FUJIE YOSHIHIKO |
| An object is to provide a coloring composition for dyeing having an excellent color, a high color optical density, excellent fixing properties, reduced bleeding, and excellent light fastness; a coloring composition for textile printing in which the coloring composition for dyeing is used for textile printing; and a compound which is preferable as a material of the coloring compositions. In addition, another object is to provide a textile printing method in which the above-described coloring composition for textile printing is used, an ink for ink jet textile printing including the above-described coloring composition for textile printing, and a dyed fabric. Provided are: a coloring composition for dyeing including a compound represented by Formula (1) shown in this specification or a salt thereof; a coloring composition for textile printing in which the coloring composition for dyeing is used for textile printing; a compound which is preferable as a material of the coloring compositions; a textile printing method in which the above-described coloring composition for textile printing is used; an ink for ink jet textile printing including the above-described coloring composition for textile printing; and a dyed fabric. | ||||||
| 11 | Anthrachinonfarbstoffe, deren Herstellung und Verwendung | EP83810367.9 | 1983-08-17 | EP0103541B1 | 1989-07-19 | Adam, Jean-Marie, Dr.; Bloch, Peter, Dr. |
| 12 | Anthraquinone dyes, their preparation and use | EP83810367 | 1983-08-17 | EP0103541A3 | 1986-08-20 | Adam, Jean-Marie, Dr.; Bloch, Peter, Dr. |
| 13 | Influencing the Near Infrared Reflectance of Dyed Textile Materials | US12934400 | 2009-03-27 | US20110027548A1 | 2011-02-03 | Rainer Nusser; Martin Leiler; Roland Lottenbach; Hans-Juergen Huebner |
| Use of the customary dyes for the type of fibre in question and using the customary dyeing and/or printing processes for the type of fibre in question for minimally reducing, retaining or increasing the NIR reflectance, preferably increasing the NIR reflectance, in the region of electromagnetic radiation of wavelength 700 nm to 1100 nm of textile material in relation to the undyed and untreated textile material, characterized in that metal-free dyes are used. | ||||||
| 14 | Isatin derivatives for coloring keratin-containing fibers | US535263 | 1995-10-30 | US5611817A | 1997-03-18 | Hinrich Moeller; Horst Hoeffkes |
| A process for coloring keratin-containing fibers by contacting the fibers with a composition containing an isatin derivative corresponding to formula I: ##STR1## wherein R.sup.1 is hydrogen, a C.sub.1-4 alkyl group, a C.sub.2-4 hydroxyalkyl group, a C.sub.2-20 acyl group, a benzyl or phenyl group, R.sup.2 is hydrogen, a C.sub.1-4 alkyl group, a C.sub.1-4 alkoxy group, a hydroxy, halogen or nitro group, X is a sulfo group --SO.sub.3 H or a carboxyl group --COOH and n is an integer from 0 to 3, including water-soluble salts thereof. | ||||||
| 15 | Anthraquinone dyes, process for their preparation, and use thereof | US521904 | 1983-08-10 | US4501592A | 1985-02-26 | Jean-Marie Adam; Peter Bloch |
| The invention relates to dyes of the formula ##STR1## wherein X is oxygen or sulfur, R is hydrogen or C.sub.1 -C.sub.4 alkyl, Y is an unsubstituted or substituted aryl radical, n is 1, 2 or 3, the benzene ring A may be substituted by halogen and the benzene rings B and D may each independently be substituted by halogen, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy or a radical of the formula --O--CH.sub.2 CH.sub.2 --O--R.sub.1, wherein R.sub.1 is hydrogen, methyl or ethyl. These dyes are suitable for dyeing or printing natural or synthetic polyamide fibres. | ||||||
| 16 | Benz-[c,d]-indolyl compounds | US974609 | 1978-12-29 | US4234488A | 1980-11-18 | Horst Harnisch; Alfred Brack |
| The invention relates to compounds of the formula ##STR1## wherein Z denotes OH or NR.sup.1 R.sup.2,R.sup.1 denotes hydrogen, alkyl, aralkyl, cycloalkyl or aryl,R.sup.2 denotes hydrogen or alkyl or, conjointly with R.sup.1, forms an alkylene chain.The dyestuffs are outstanding suitable for the dyeing of polyester fibres. The yellow and reddish dyeings are distinguished by good fastness to light. | ||||||
| 17 | Benzodipyrrole dyestuffs | US887201 | 1978-03-15 | US4122087A | 1978-10-24 | Colin William Greenhalgh; John Laurence Carey; David Francis Newton |
| Substituted 2,6-dioxo-2,6-dihydrobenzo[1:2-b, 4:5-b']difurans or -dipyrroles and processes for their manufacture. The compounds are dyestuffs which are particularly useful in the form of aqueous dispersions for application to polyester textile materials. | ||||||
| 18 | Reduced-staining colorant system | US655346 | 1976-02-05 | US4110238A | 1978-08-29 | Robert J. Lala |
| A dye composition is disclosed together with methods for its use and detergent compositions employing the combination. The dye composition is a mixture of anthraquinone dyes suitable for use with liquid laundry detergents. The composition substantially reduces the undesirable fabric staining characteristic of a detergent in which the dye is employed, while still retaining the ability to blue the fabric. Further, the color value of the detergent product is maintained at a desirable level. The composition is a combination of an oil soluble dye such as 1,4-bis(2-ethylhexylamino)-anthraquinone (C.I. Solvent Blue 58) with a water soluble dye such as 1-amino-2-sulfo, 4-(2-sulfo-para toluidino) anthraquinone sodium salt (C.I. Acid Blue 145) and/or 1,4-bis(3-sodium sulfonate mesitylidino) anthraquinone (C.I. Acid Blue 80). | ||||||
| 19 | Reduced-staining colorant system for liquid laundry detergents | US574487 | 1975-05-05 | US3958928A | 1976-05-25 | Robert J. Lala |
| A dye composition is disclosed together with methods for its use and detergent compositions employing the combination. The dye composition is a mixture of anthraquinone dyes suitable for use with liquid laundry detergents. The composition substantially reduces the undesirable fabric staining characteristic of a detergent in which the dye is employed, while still retaining the ability to blue the fabric. Further, the color value of the detergent product is maintained at a desirable level. The composition is a combination of an oil soluble dye such as 1,4-bis(2-ethylhexylamino)-anthraquinone (C.I. Solvent Blue 58) with a water soluble dye such as 1-amino-2-sulfo, 4-(2-sulfo-para toluidino) anthraquinone sodium salt (C.I. Acid Blue 145) and/or 1,4-bis(3-sodium sulfonate mesitylidino) anthraquinone (C.I. Acid Blue 80). | ||||||
| 20 | Anthraquinone dyes,their production and use | US66155167 | 1967-08-18 | US3580933A | 1971-05-25 | GUENTHARD JACQUES |
| ANTHRAQUINONE DYES OF THE FORMULA
1-(E-NH-),4-(F-NH-)-9,10-ANTHRAQUINONE WHEREIN: E REPRESENTS A SULFONATED CARBOARYLAMIDEO-ALKYLENE GROUP, F REPRESENTS E OR AN ALKYL-OR CYCLOALKYL RADICAL, AND THE RING B MAY BEAR FURTHER SUBSTITUENTS. |
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