| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 21 | 폴리아미드 및 양모용 산성 염료 혼합물 | KR1020147001073 | 2012-06-13 | KR1020140053956A | 2014-05-08 | 지버,헬무트; 누써,라이너; 마라찌,리노 |
| 본 발명은, a) 일반 식 (A)를 갖는 하나 이상의 염료 A를 20 내지 95% 중량 퍼센트로, b) 일반 식 (B)를 갖는 하나 이상의 염료 B를 5 내지 80중량 퍼센트로 함유하는 산성 염료 혼합물에 관한 것이다. | ||||||
| 22 | 은 함유 항균 산성 염료와 그의 제조 방법 및 그를 이용한항균 섬유 | KR1020050014915 | 2005-02-23 | KR1020060094190A | 2006-08-29 | 박성희 |
| 본 발명은 강력한 항균성 반응기로서 은 함유 설폰아미드계 항균제에 염료 중간체가 결합되어 하기 화학식 1의 구조를 갖는 은 함유 항균 산성 염료 및 그의 제조방법에 관한 것이다. (화학식 1) (상기식에서, R은 SO 3 H 또는 SO 3 Na이다) 본 발명의 은 함유 항균 산성 염료 화합물은 청색을 갖추고 있어 혼합시 다양한 색상을 발현하고, 이를 이용하여 섬유를 염색하면 강력한 항균성을 나타내어 미생물의 서식이나 증식을 억제하여 전염성질환 예방, 악취예방, 섬유의 오염과 취화를 방지할 수 있는 기능성 항균 섬유 제품을 제조할 수 있다. 은 함유, 항균 산성 염료, 설폰아미드, 항균 섬유, 실버설파다이아진, 항균성. | ||||||
| 23 | SÄUREFARBSTOFFMISCHUNGEN FÜR POLYAMID UND WOLLE | EP12727600.4 | 2012-06-13 | EP2721112A1 | 2014-04-23 | SIEBER, Helmut; NUSSER, Rainer; MARAZZI, Rino |
| The invention relates to an acid dye mixture comprising a) between 20 and 95 wt. % of at least one dye A of general structure (A), and b) between 5 and 80 wt. % of at least one dye B of general structure (B). | ||||||
| 24 | INFLUENCING THE NEAR INFRARED REFLECTANCE OF DYED TEXTILE MATERIALS | EP09725488.2 | 2009-03-27 | EP2262945B1 | 2013-03-13 | NUSSER, Rainer; LEILER, Martin; LOTTENBACH, Roland; HUEBNER, Hans-Jürgen |
| 25 | INFLUENCING THE NEAR INFRARED REFLECTANCE OF DYED TEXTILE MATERIALS | EP09725488.2 | 2009-03-27 | EP2262945A1 | 2010-12-22 | NUSSER, Rainer; LEILER, Martin; LOTTENBACH, Roland; HUEBNER, Hans-Jürgen |
| 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. | ||||||
| 26 | VERFAHREN ZUM BEDRUCKEN VON TEXTILEN FASERMATERIALIEN NACH DEM TINTENSTRAHLDRUCK-VERFAHREN | EP99931249.9 | 1999-07-05 | EP1102883A1 | 2001-05-30 | LACROIX, Roger; SCHEIBLI, Peter; MHEIDLE, Mickael |
| The invention relates to a method for printing fibrous textile materials using the ink jet technique. The method is characterised in that said fibrous materials are printed with an aqueous ink which contains at least one acidic dye as described in claim no. 1 and has a viscosity of 1 to 40 mPa.s | ||||||
| 27 | WASSERLÖSLICHE CHINACRIDONE | EP98913688.2 | 1998-03-09 | EP0970149A1 | 2000-01-12 | ETZBACH, Karl-Heinz; KRANZ, Carolin; SENS, Rüdiger |
| This invention concerns water soluble quinacridones of general formula (I) in which Mo is a lithium, sodium, potassium or ammonium cation, and, independent of each other, R?1, R2, R3, and R4¿ are hydrogen, C¿1?-C8-alkyl, C1-C8-alkoxy, carboxyl, C1-C4-alkoxycarbonyl, sulfamoyl, mono- or di-(C1-C4)-alkylsulfamoyl, carbamoyl, mono- or di-(C1-C4)-alkylcarbamoyl, unsubstituted or substituted mono- or diphenylsulfamoyl, unsubstituted or substituted mono- or diphenylcarbamoyl, halogen, nitro or cyano, n is 0, 1, or 2, and m is 0, 1 or 2, and the sum n + m is at least 1. Said quinacridones are used to dye and print natural and synthetic fiber materials. | ||||||
| 28 | ISATINDERIVATE ZUM FÄRBEN VON KERATINHALTIGEN FASERN | EP94915085.8 | 1994-04-21 | EP0695163B1 | 1997-03-05 | MÖLLER, Hinrich; HÖFFKES, Horst |
| The invention concerns the use of certain isatin derivatives containing sulphonic or carboxylic groups to dye keratin-containing fibres, in particular the human hair, as well as dyes containing such isatin derivatives. The invention particularly concerns dyes containing the above-mentioned isatin derivatives in combination with certain amino-compounds. | ||||||
| 29 | ISATIN DERIVATIVES FOR DYEING KERATIN-CONTAINING FIBRES | EP94915085.0 | 1994-04-21 | EP0695163A1 | 1996-02-07 | MÖLLER, Hinrich; HÖFFKES, Horst |
| The invention concerns the use of certain isatin derivatives containing sulphonic or carboxylic groups to dye keratin-containing fibres, in particular the human hair, as well as dyes containing such isatin derivatives. The invention particularly concerns dyes containing the above-mentioned isatin derivatives in combination with certain amino-compounds. | ||||||
| 30 | NOVEL COMPOUND, COLORING COMPOSITION FOR DYEING OR TEXTILE PRINTING, INK FOR INK JET TEXTILE PRINTING, METHOD OF PRINTING ON FABRIC, AND DYED OR PRINTED FABRIC | US15934365 | 2018-03-23 | US20180208773A1 | 2018-07-26 | Takashi IIZUMI; Kazunari YAGI; Keiichi TATEISHI |
| Provided are a compound represented by any one of Formulae (1) to (3) described in the specification, a coloring composition for dyeing or textile printing including the compound, an ink for ink jet textile printing, a method of printing on fabric, and a dyed or printed fabric. | ||||||
| 31 | COLORING COMPOSITION FOR TEXTILE PRINTING, TEXTILE PRINTING METHOD, INK FOR INK JET TEXTILE PRINTING, AND DYED FABRIC | US15592749 | 2017-05-11 | US20170247544A1 | 2017-08-31 | Kazunari YAGI; Keiichi TATEISHI; Takashi IIZUMI; Akihiro HAKAMATA; Yoshihiko FUJIE |
| 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. | ||||||
| 32 | Process For Dyeing Carpets With Unused Yarns | US13277484 | 2011-10-20 | US20120198634A1 | 2012-08-09 | Robert D. Hutchison; Robert W. Brinkley |
| Overdyed carpets, as well as other textiles, and methods of producing the same are provided. Overdyeing can be performed on predyed and/or undyed fibers to produce an overdyed carpet with a predominant hue throughout. Predyed fibers can differ in hue, saturation, or value, or any combination thereof from each other and/or from the overdye. The overdyed carpet can include at least one auxiliary chemical. A single auxiliary chemical or a combination of auxiliary chemicals can provide stain resistance, color fastness, and/or bleach resistance, or any combination thereof. These carpets and methods provide aesthetic, financial, and environmental benefits by allowing for utilization of waste fiber, yarn, carpet, and other textiles that would otherwise require resale at substantial discount or landfill disposal. | ||||||
| 33 | Water-soluble Quinacridones | US380615 | 1999-09-17 | US6152968A | 2000-11-28 | Karl-Heinz Etzbach; Carolin Kranz; Rudiger Sens |
| The use of water-soluble quinacridones of the formula I ##STR1## where M.sup..sym. is a lithium, sodium, potassium or ammonium cation,R.sup.1, R.sup.2, R.sup.3 and R.sup.4 independently are hydrogen, C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxy, carboxyl, C.sub.1 -C.sub.4 -alkoxycarbonyl, sulfamoyl, mono- or di-(C.sub.1 -C.sub.4)-alkylsulfamoyl, carbamoyl, mono- or di-(C.sub.1 -C.sub.4)-alkylcarbamoyl, unsubstituted or substituted mono- or diphenylsulfamoyl, unsubstituted or substituted mono- or diphenylcarbamoyl, halogen, nitro or cyano,n is 0, 1 or 2 andm is 0, 1 or 2 and the sum n+m is at least 1,for dyeing and printing natural and synthetic fiber material. | ||||||
| 34 | Dye mixtures and the use thereof | US207540 | 1998-12-08 | US6030420A | 2000-02-29 | Jean-Marie Adam |
| The invention relates to dye mixtures comprising at least one dye of formula (1) ##STR1## wherein R.sub.1 is hydrogen, C.sub.1 -C.sub.4 alkyl or C.sub.1 -C.sub.4 alkoxy and R.sub.2 is hydrogen or C.sub.1 -C.sub.4 alkyl, together with at least one dye of formula (2) ##STR2## wherein R.sub.3 is hydrogen, C.sub.1 -C.sub.4 alkyl or C.sub.1 -C.sub.4 alkoxy, R.sub.4 is hydrogen or C.sub.1 -C.sub.4 alkyl and R.sub.5 is C.sub.2 -C.sub.6 alkyl uninterrupted or interrupted by oxygen, with the proviso that R.sub.1 is not methyl when R.sub.2, R.sub.3 and R.sub.4 are hydrogen and R.sub.5 is ethyl.The dye mixtures are suitable for dyeing or printing natural or synthetic polyamide fibre materials, especially in combination with other dyes and especially from short liquors. The dye mixture is distinguished by generally good properties, especially good uptake and good solubility. | ||||||
| 35 | Amino acid salts of anionic dyestuffs which have high solubility in organic solvents | US858446 | 1977-12-07 | US4204879A | 1980-05-27 | Keith N. Paskins; Duncan C. Redman; Ian D. Turner |
| This invention concerns a range of amino-acid salts of anionic dyestuffs which have a high solubility in organic solvents, particularly oxygenated, halogenated and amido organic solvents. The amino-acid dyestuff salts have the general formula:[Am.sup.+ ].sub.n-g A.sup.n- [Cat.sup.+ ].sub.q (1)wherein Am.sup.+ is an amino-acid portion of the formula: ##STR1## in which L.sup.2 is a radical of the formula:--(CR.sup.4 R.sup.5).sub.x --where R.sup.4 and R.sup.5 are each, independently of one another, selected from the group consisting of hydrogen, linear and branched lower alkyl, unsubstituted and substituted aryl and unsubstituted and substituted amino, and x is an integer,R.sup.1, R.sup.2 and R.sup.3 are each, independently of one another, selected from the group consisting of hydrogen, alkyl, aryl, alkaryl, aralkyl and the radical of the formula:--L.sup.1 --COOHwhere L.sup.2 is any of the radicals of L.sup.1, and which alkyl radicals and moities of R.sup.1, R.sup.2 and R.sup.3 are selected from the group consisting of unsubstituted and substituted alkyl radicals and moieties and uninterrupted alkyl radicals and moieties and alkyl radicals and moieties interrupted by at least one hetero atom selected from the group consisting of oxygen and nitrogen, provided that each of R.sup.1, R.sup.2 and R.sup.3 are not the group of the formula:--L.sup.2 --COOHat one and the same time,A.sup.n- is an anionic dyestuff portion having an n-fold negative charge,Cat.sup.+ is a cationic radical,n is an integer,q is any of 0 and an integer, and when q is greater than 1 then each of the cations may be the same or different. | ||||||
| 36 | Dyeing of polyamide textiles and anthraquinone dyestuffs therefor | US893730 | 1978-04-05 | US4188187A | 1980-02-12 | Roland Mislin; Karl-Ulrich Steiner |
| A process for dyeing or printing natural or synthetic polyamide textile substrates comprising employing, as dyestuff, a compound of formula I, ##STR1## in which R is hydrogen, methyl or ethyl,R.sub.1 is hydrogen, methyl or ethyl, andthe ring A is unsubstituted or monosubstituted by halogen, (C.sub.1-2)alkyl, (C.sub.1-2)alkoxy or alkyl(C.sub.1-2)carbonylamino or disubstituted by methyl groups,in free acid or salt form. | ||||||
| 37 | Benz-(C,D)-indolyl compounds | US890688 | 1978-03-27 | US4147865A | 1979-04-03 | 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. | ||||||
| 38 | Process for the dyeing or printing of polyacrylonitrile material | US778655 | 1977-03-16 | US4123222A | 1978-10-31 | Peter Loew |
| A process is described for the dyeing or printing of polyacrylonitrile materials, which process comprises the use of dyes of the formula ##STR1## wherein R.sub.1 represents a low-molecular, straight-chain alkyl group, R.sub.2 and R.sub.3 independently of one another each represent a low-molecular alkyl group, R.sub.4 represents an aralkyl group, n represents 2 or 3, and X.sup..crclbar. represents an anion.The dyeings obtained are distinguished by good build-up properties of the dyes, and the dyes are particularly suitable for trichromatic dyeings. | ||||||
| 39 | Benzodifuran dyestuffs | US773229 | 1977-03-01 | US4115404A | 1978-09-19 | Colin William Greenhalgh; John Laurence Carey; David Francis Newton |
| Substituted 2,6-dioxo-2,6-dihydrobenzo[1:2-b, 4:5-b.sup.1 ]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. | ||||||
| 40 | Halosolvent dyeing process for polyester with cationic dyes having sulfosuccinate anions | US634437 | 1975-11-24 | US4063889A | 1977-12-20 | Erik Kissa |
| In an exhaustion process for dyeing unmodified or acid-modified polyester fibers, the fibers are introduced into a dye bath comprising a chlorinated hydrocarbon solvent, a water-insoluble salt of a cationic dye and a C.sub.6-13 alkyl sulfosuccinate anion, from 0.05 to 1.0% based on the total weight of the dyebath of at least one low molecular weight carboxylic acid, a solvent-soluble quaternary ammonium salt of an arylsulfonic acid and optionally additional processing assistants, after which the cationic dye salt is exhausted onto the unmodified or acid-modified polyester by heating the dyebath at a temperature of from 110.degree. to 170.degree. C for from 0.5 to 3 hours, with the proviso that, in the case of the acid-modified polyester fibers, from 0.01 to 0.10% based on the total weight of the dyebath of water must also be present in the dyebath. Good to excellent penetration of and buildup on the polyester fibers are obtained. | ||||||
QQ群二维码
意见反馈
意见反馈