子分类：
| 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 | 一种MFPET纤维染色的平幅退浆工艺 | CN201610744293.3 | 2016-08-29 | CN106087487A | 2016-11-09 | 张建国; 吴学芬; 高骏超; 林兴旺 |
| 一种MFPET纤维染色的平幅退浆工艺，所述平幅退浆工艺使用的平幅退浆助剂每升含有下列材料：液碱20~30克；乳化分散退浆剂M1~2克；三聚磷酸钠1.8~2.2克；除油剂F1.8~2.2克。本发明的处理效果好，操作方便。 | ||||||
| 2 | 一种摇粒绒和仿超柔绒双面绒布 | CN201710552851.0 | 2017-07-07 | CN107313200A | 2017-11-03 | 伍允程; 龚小平 |
| 本发明涉及摇粒绒和仿超柔绒双面绒布，正面摇粒绒布层的原料为150D/144F涤纶长丝，中间底布层的原料为100D/36F涤纶长丝，反面仿超柔绒布层的原料为蒸纱过的75D/144F FDY涤纶半光丝，中间底布层将正反面牢固地连接在一起，三种材料相互配合，使正反面的绒毛密实丰满，反面选用蒸纱过的75D/144F FDY涤纶半光丝能够使仿超柔绒面柔软、细腻、保暖、滑爽、光泽度高，并最终在烫光工艺下形成仿超柔绒效果。烫光工艺为对仿超柔绒进行两次烫光，首次是对白胚烫光，可以采用较高温度，使绒毛顺直光亮，二次烫光是在染色工艺之后进行，采用较低的烫光温度以防止色牢度降低，同时再次获得顺直光亮的绒毛，通过两次烫光形成仿超柔绒效果，从而制得摇粒绒和仿超柔绒双面绒布。 | ||||||
| 3 | 一种拉伸渐变色经编材料的制备方法 | CN201610482463.5 | 2016-06-28 | CN106012272A | 2016-10-12 | 张建福; 马月娟; 孙云浩; 周珏; 封亚鸿 |
| 本发明公开了一种拉伸渐变色经编材料的制备方法，其中织造步骤：对整经好的纱线采用HK3‑1型号经编机进行织造，垫纱方式和纱线配置为GB1：2‑3/1‑0//满穿，所编织的线圈及延展线均显露在织物的表面；GB2：1‑0/1‑2//满穿同GB1进行反向垫纱；GB3：0‑0/2‑2//满穿，垫纱方向与GB2相同，与GB1相反,所编织的纱线交织于GB1延展线底部，同时控制纬密WPC为24‑25r/cm，利用衬纬组织不成圈的特点，使纱线在自然回缩状态下不显露，隐于织物之中。本发明制备的拉伸渐变色经编材料在受力拉伸情况下显现出不同的颜色，而作用力的不同其体现出的颜色深浅也不同。 | ||||||
| 4 | 制造塑料制品的方法 | CN201580041614.7 | 2015-07-28 | CN106661251A | 2017-05-10 | 科内利斯·约翰内斯·赫拉尔杜斯·马里亚·范佩尔; 迪尔克·阿尔特·诺登赫拉夫 |
| 公开了一种制造塑料制品的方法。根据这种方法，塑料制品由包含第一聚合物组分的热塑性组合物形成，第一聚合物组分是(i)聚(硅氧烷‑碳酸酯)共聚物，(ii)具有软嵌段酯单元的聚(脂肪族酯)‑聚碳酸酯，衍生自包含α,ωC6‑20脂肪族二羧酸或其衍生物、二羟基芳香族化合物和碳酸酯源的单体，(iii)热塑性聚氨酯，(iv)热塑性聚氨酯，或包含任何前述物质的组合。然后通过使制品的表面与超临界流体二氧化碳接触而将诸如光致变色染料的添加剂载入塑料制品中，超临界流体二氧化碳包含溶解或分散于其中的添加剂。 | ||||||
| 5 | 一种MFPET纤维染色的前处理工艺 | CN201610744292.9 | 2016-08-29 | CN106087486A | 2016-11-09 | 段佳; 吴学芬; 沈丹峰; 朱韦伟 |
| 一种MFPET纤维染色的前处理工艺，所述前处理工艺包括平幅退浆工艺和机缸复炼工艺，所述平幅退浆工艺使用的平幅退浆助剂每升含有下列材料：液碱20~30克；乳化分散退浆剂M1~2克；三聚磷酸钠1.8~2.2克；除油剂F1.8~2.2克；所述机缸复炼工艺使用的机缸复炼助剂每升含有下列材料：纯碱3~5克；氧化退浆剂D1.8~2.2克；去油灵1011.8~2.2克；除油剂F1.8~2.2克。本发明的前处理工艺使MFPET纤维染色效果更好、染色牢度更高。 | ||||||
| 6 | JPS4827237B2 - | JP4640871 | 1971-06-28 | JPS4827237B2 | 1973-08-20 | |
| 1324615 Dyeing processes FARBWERKE HOECHST AG 30 June 1971 [30 June 1970] 30693/71 Heading D1B Hydrophobic fibres, e.g. cellulose 2¢ and tri-acetates, polyacrylonitrile, polyamide, polyurethane and polyesters are dyed or printed at temperatures above 50‹C in the presence of a protein donor with an aqueous solution of a dye of formula F-X-CO-N-SO 3 M in M in which F is the radical of a water-insoluble dyestuff, M is an alkali metal ion or atom or ammonium ion, the bond between M and the nitrogen atom or sulph oxide group being ionic or covalent, X is -O- or -S- or -NR- in which R is H an alkyl or aryl group, an acyl or a sulphonyl group, preferably alkyl sulphonyl or arylsulphonyl group. The dyeing may be effected by exhaustion processes or by podding or printing followed by steaming or thermosolisation, carriers may also be used. Proton donors include ammonium sulphate, magnesium chloride, sodium N-benzyl-sulphanilate, tartaric acid dialkyl esters and phosphoric acid trialkyl ester. | ||||||
| 7 | Piperazin-2,5-dion und Piperazin-2-on Derivate | EP91113808.9 | 1991-08-17 | EP0477528A1 | 1992-04-01 | Diblitz, Christina, Dr.; Höchstetter, Hans, Dr. |
Verbindungen der Formeln
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| 8 | METHOD OF MAKING PLASTIC ARTICLE | EP15770644.1 | 2015-07-28 | EP3174918A1 | 2017-06-07 | VAN PEER, Cornelis Johannes Gerardus Maria; NOORDEGRAAF, Dirk Aart |
| A method of making a plastic article is disclosed. According to this method, a plastic article is formed from a thermoplastic composition that includes a first polymer component that is (i) a poly(siloxane-carbonate) copolymer, (ii) a poly(aliphatic ester)-polycarbonate having soft block ester units, derived from monomers including an alpha, omega C6-20 aliphatic dicarboxylic acid or derivative thereof, a dihydroxyaromatic compound, and a carbonate source, (iii) a thermoplastic polyurethane, (iv) a thermoplastic polyurethane, or a combination comprising any of the foregoing. An additive such as a photochromic dye is then loaded into the plastic article by contacting a surface of the article with supercritical fluid carbon dioxide comprising the additive dissolved or dispersed therein. | ||||||
| 9 | METHOD FOR DYEING TEXTILES USING METALLIC YARN AND POLYESTER YARN AND TEXTILE MANUFACTURED THEREBY | EP12849539 | 2012-05-30 | EP2781647A4 | 2015-08-26 | WOO JUNG HA; KIM SUN JIN; CHO SUNG HYUN |
| 10 | Piperazin-2,5-dion und Piperazin-2-on Derivate | EP91113808.9 | 1991-08-17 | EP0477528B1 | 1995-12-13 | Diblitz, Christina, Dr.; Höchstetter, Hans, Dr. |
| 11 | METHOD FOR DYEING A TRANSPARENT ARTICLE MADE OF A POLYMERIC SUBSTRATE WITH GRADIENT TINT | EP14803242.8 | 2014-07-30 | EP3174698A1 | 2017-06-07 | BHANGALE, Sunil Madhukar |
| A method for dyeing a transparent article made of a polymeric substrate with gradient tint comprising: a) a first step of photodegrading the polymeric substrate (1) of the transparent article, by irradiation (3) of at least one first surface of the article to UV radiations to produce a gradiently photodegraded surface layer of the polymeric substrate, and b) a second step of dyeing said first face of the article with a dyeing agent so as to diffuse said dyeing agent into the gradiently photodegraded surface layer of the polymeric substrate. | ||||||
| 12 | METHOD FOR DYEING TEXTILES USING METALLIC YARN AND POLYESTER YARN AND TEXTILE MANUFACTURED THEREBY | EP12849539.7 | 2012-05-30 | EP2781647A1 | 2014-09-24 | WOO, Jung Ha; KIM, Sun Jin; CHO, Sung Hyun |
A method for manufacturing dyed woven or knitted fabric includes preparing woven or knitted fabric using metallic yarn and normal-pressure dyeing polyester yarn having an elasticity modulus of 400 to 600 kg/mm2 and an elongation of 30 to 40%, fabricating a dye bath by putting a dye solution obtained by dispersing a dye in water, dyeing the woven or knitted fabric by putting the prepared woven or knitted fabric into the fabricated dye bath, raising a temperature of the dye bath starting from 35 to 45°C for 30 to 50 minutes at a rate of 1.2 to 1.5 °C/min, and maintaining the heated dye bath at 90 to 100°C for 15 to 25 minutes, and washing the dyed woven or knitted fabric. The dyed woven or knitted fabric has a light reflection reduction rate of 20% to 30%. |
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| 13 | Disazo compounds and staining using it | JP9436386 | 1986-04-23 | JPH0619044B2 | 1994-03-16 | HIMENO KYOSHI; HIBARA TOSHIO |
| 14 | Heterocyclic compound | JP23886691 | 1991-08-27 | JPH04257566A | 1992-09-11 | KURISUCHINA DEIBURITSUTSU; HANSU HEHISHIYUTETSUTAA |
| PURPOSE: To provide a heterocyclic compd. useful as a coloring agent for coloring high-polymer org. materials and more particularly plastics by pigments and dyes, and the intermediate thereof. CONSTITUTION: The compd. of formula I (R 1, R 2 are alkyl, cycloalkyl, aralkyl, aryl, heterocyclic group; R 1, R 4 are H, alkyl, aryl, cycloalkyl, aralkyl, heterocyclic group) or the compd. of formula II (X', Y' are O, S, NR 5, part of 5- or 6-membered heterocycle; R 5 is H, alkyl, aryl, etc.). The compd. of the formula I is obtd. by bringing the compd. of formula III (R 12 is H, COR 5) and the compd. of the formula R 1-COCOOR 3 into reaction at 30 to 130°C in the presence of a base (e.g.; triethylamine). The compd. of the formula II is obtd. by heating the compd. of the formula I in a melt or a solvent of a high b. p. COPYRIGHT: (C)1992,JPO | ||||||
| 15 | Disazo compound and method for dyeing using same | JP9436386 | 1986-04-23 | JPS62250060A | 1987-10-30 | HIMENO KIYOSHI; HIBARA TOSHIO |
| NEW MATERIAL:A water-soluble disazo compound expressed by formula I (Dz is benzene ring or naphthalene ring which may be substituted with methyl, methoxy or sulfonic acid group; R is H, methyl, carbamoyl or COOH; A - is anion) as a free acid. EXAMPLE: The compound of formula II. USE: A dye for coloring cellulosic fiber, polyamide, wool, silk, etc., in orange to scarlet color. Suitable especially for the use in combination with a disperse dye for polyester in a one-bath one-stage dyeing of a P/C fiber. Suitable also as a dye for ink jet printer. PREPARATION: For example, 1mol of the dye of formula III is condensed with 1mol of the dye of formula IV to form a disazo compound of formula V, which is made to react with the compound of formula VI in an aqueous medium at 70W100°C. COPYRIGHT: (C)1987,JPO&Japio | ||||||
| 16 | JPS516264B1 - | JP5039466 | 1966-08-02 | JPS516264B1 | 1976-02-26 | |
| 17 | JPS472098A - | JP4640871 | 1971-06-28 | JPS472098A | 1972-02-01 | |
| 1324615 Dyeing processes FARBWERKE HOECHST AG 30 June 1971 [30 June 1970] 30693/71 Heading D1B Hydrophobic fibres, e.g. cellulose 2¢ and tri-acetates, polyacrylonitrile, polyamide, polyurethane and polyesters are dyed or printed at temperatures above 50‹C in the presence of a protein donor with an aqueous solution of a dye of formula F-X-CO-N-SO 3 M in M in which F is the radical of a water-insoluble dyestuff, M is an alkali metal ion or atom or ammonium ion, the bond between M and the nitrogen atom or sulph oxide group being ionic or covalent, X is -O- or -S- or -NR- in which R is H an alkyl or aryl group, an acyl or a sulphonyl group, preferably alkyl sulphonyl or arylsulphonyl group. The dyeing may be effected by exhaustion processes or by podding or printing followed by steaming or thermosolisation, carriers may also be used. Proton donors include ammonium sulphate, magnesium chloride, sodium N-benzyl-sulphanilate, tartaric acid dialkyl esters and phosphoric acid trialkyl ester. | ||||||
| 18 | METHOD FOR MANUFACTURING DYED WOVEN OR KNITTED FABRIC USING METALLIC YARN AND POLYESTER YARN AND FABRIC MANUFACTURED USING THE METHOD | US14358034 | 2012-05-30 | US20140310889A1 | 2014-10-23 | Jung Ha Woo; Sun Jin Kim; Sung Hyun Cho |
| A method for manufacturing dyed woven or knitted fabric includes preparing woven or knitted fabric using metallic yarn and normal-pressure dyeing polyester yarn having an elasticity modulus of 400 to 600 kg/mm2 and an elongation of 30 to 40%, fabricating a dye bath by putting a dye solution obtained by dispersing a dye in water, dyeing the woven or knitted fabric by putting the prepared woven or knitted fabric into the fabricated dye bath, raising a temperature of the dye bath starting from 35 to 45° C. for 30 to 50 minutes at a rate of 1.2 to 1.5° C./min, and maintaining the heated dye bath at 90 to 100° C. for 15 to 25 minutes, and washing the dyed woven or knitted fabric. The dyed woven or knitted fabric has a light reflection reduction rate of 20% to 30%. | ||||||
| 19 | Method of dyeing a semi-finished product | US11633797 | 2006-12-05 | US20070079453A1 | 2007-04-12 | Robert Pyles; Rick Archey; David Derikart |
| A method of dyeing a semi-finished product is disclosed. The method comprise: (a) providing a semi-finished product selected from the group consisting of powders, pellets and strands, that contain at least one thermoplastic polymer; (b) immersing said semi-finished product in a dye bath comprising, (i) at least one dye, (ii) water, (iii) at least one carrier represented by the following general formula I, (I) R1[O(CH2)n]mOR2 where R1 and R2 independently one of the other denote H, C1-18-alkyl, benzyl, benzoyl or phenyl radicals which may be substituted in the aromatic ring by alkyl and/or halogen, n is 2 or 3 and m is 1 to 35, and (iv) a diol selected from at least one of linear or branched C2-C20 aliphatic diols, poly(C2-C4 alkylene glycol), cycloaliphatic diols having from 5 to 8 carbon atoms in the cyclic ring, monocyclic aromatic diols, bisphenols and hydrogenated bisphenols; (c) retaining said semi-finished product in said bath for a period of time sufficient to form a dyed semi-finished product; and (d) removing said dyed semi-finished product from said bath. | ||||||
| 20 | Process of producting fast dyeings on cellulose esters and ethers and the dyed fiber obtained thereby | US30353839 | 1939-11-09 | US2243213A | 1941-05-27 | GEORG KRANZLEIN; JOSEF MULLER CARL; WERNER KIRST |
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