| 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 | Colored contact lenses and method of making same | US09658592 | 2000-09-08 | US06337040B1 | 2002-01-08 | Ashok R. Thakrar; Bradley K. Overmyer; William E. Meyers |
| Optical lenses and methods of preparing the same, in which an active material encapsulated in resin capsules is impregnated in said lens, adjacent an optical surface thereof. The active material may be a coloring material for producing a printed color pattern in the iris or other areas of the lens, or it may be a therapeutic agent. | ||||||
| 22 | Colored contact lenses and method of making same | US08143373 | 1993-10-26 | US06284161B1 | 2001-09-04 | Ashok R. Thakrar; Bradley K. Overmyer |
| Optical lenses and methods of preparing the same, in which an active material encapsulated in resin capsules is impregnated in said lens, adjacent an optical surface thereof. The active material may be a coloring material for producing a printed color pattern in the iris or other areas of the lens, or it may be a therapeutic agent. | ||||||
| 23 | Polymeric colorant and colored material for ocular lens using the colorant | US09251377 | 1999-02-17 | US06242551B1 | 2001-06-05 | Akira Tsuzuki; Kazuharu Niwa; Tatsuya Ojio |
| A polymeric colorant represented by the following formula: A1—N═N—A2—O—(CH2)n—X wherein, A1 represents an aryl group which may have a substituent group, A2 represents an arylene group which may have a substituent group, X represents one of an acryloyloxy group, a methacryloyloxy group, a vinylphenyl group, a vinylphenyloxy group, and a vinylphenylalkyloxy group whose alkyl portion has 1-5 carbon atoms, and n is an integer of 1-5, and a colored material for an ocular lens which uses the polymeric colorant is also disclosed. | ||||||
| 24 | ポリマーの着色のための非移染性の着色共重縮合物 | JP2012530215 | 2010-09-15 | JP5693586B2 | 2015-04-01 | トーマス ルーフ; トーマス アイヒェンベルガー; ペーター ズッター; クリストフ クレープス; ウアズラ ルーターバッハー |
| 25 | Polymeric dye | JP2010506888 | 2008-04-25 | JP2010526897A | 2010-08-05 | クレーマー，クリスティアン; フローリング，ベアーテ; ミュラー，マルティン; ルイス リグス，リヒャルト |
| A highly crosslinked polysiloxane dye comprising at least 10 Si atoms, including at least one moiety of the formula (I) whose open Si-bonds each are linked to an oxygen atom and open O-bond is linked to a silicon atom in the rest of the polysiloxane, and wherein T is a direct bond or an organic spacer group such as C1-C18alkylene, C2-C12alkenylene, C5-C10cycloalkylene, C5-C10arylene, —C5-C10arylene-(C1-C10alkylene)- each of which may be end-capped towards the linkage to Dye by CO, COO, NR1, CONR1, NR1CONR1, CS, CSS, CSNR1, NR1CSNR1, O, S, SO, SO2, C5-C10cycloalkylene, C5-C10arylene; or T is C3-C18alkylene interrupted, and optionally end-capped towards the linkage to Dye, by CO, COO, NR1, CONR1, NR1CONR1, CS, CSS, CSNR1, NR1CSNR1, O, S, SO, —SO2—, C5-C10cycloalkylene, C5-C10arylene; or is CO; (CH2CH2—O)1-5; COO; N(R1); CON(R1); O; S; SO; SO2; R1 is hydrogen; unsubstituted or substituted, straight-chain or branched, monocyclic or polycyclic, interrupted or uninterrupted C1-C14alkyl; C2-C14alkenyl; C6-C10aryl; C6-C10aryl-C1-C10alkyl; or C5-C10alkyl(C5-C10aryl); and Dye is a residue of an organic dye, is useful for dyeing of organic materials, such as keratin-containing fibers, wool, leather, silk, cellulose or polyamides. | ||||||
| 26 | Polymerizable dyes and colorings ocular lens material using the same | JP5880797 | 1997-03-13 | JP3805853B2 | 2006-08-09 | 一晴 丹羽; 達也 小塩; 章 都築 |
| A polymeric colorant represented by the following formula:wherein, A1 represents an aryl group which may have a substituent group, A2 represents an arylene group which may have a substituent group, X represents one of an acryloyloxy group, a methacryloyloxy group, a vinylphenyl group, a vinylphenyloxy group, and a vinylphenylalkyloxy group whose alkyl portion has 1-5 carbon atoms, and n is an integer of 1-5, and a colored material for an ocular lens which uses the polymeric colorant is also disclosed. | ||||||
| 27 | Used for the polymer dye and textile dyeing | JP52804696 | 1996-03-13 | JPH11505553A | 1999-05-21 | ヴァハター，ロルフ; カーレ，イェルク; ローズ，デイビッド |
| (57)【要約】 本発明は、カチオン性バイオポリマー（例えばキトサン）と、塩基性基（好適にはハロゲン基）を有する染料との縮合によって得られる新規ポリマー染料に関する。 ポリマー染料は、繊維上に膜として広がり、容易に洗い流すことができる。 | ||||||
| 28 | Polymeric dye | JP2010506888 | 2008-04-25 | JP5518697B2 | 2014-06-11 | クレーマー，クリスティアン; ルイス リグス，リヒャルト; フローリング，ベアーテ; ミュラー，マルティン |
| 29 | Industrial fabric with a thermochromic sensor | JP2009554626 | 2008-02-29 | JP2010522283A | 2010-07-01 | オコナー・ジョゼフ・ジー． |
| 本発明は、工業的熱プロセス、そのようなプロセスにおいて使用される工業用布、その工業用布の製造、及び／又は製造されたあるいはその布の上に運ばれた製品の熱プロファイルを調べる際に使用されることが可能な、プロセス制御の助けとして用いられるポリチオフェンなどのサーモクロミック材料が組み込まれた、エンドレスベルト及び布に向けられている。 | ||||||
| 30 | Light absorbing prepolymer and a method of manufacturing the same will be used in the colored contact lenses | JP2009534708 | 2007-10-31 | JP2010508547A | 2010-03-18 | フェノリ・クリストファー; モロック・ジュニア・フランク・エフ |
| 本発明は、約７，０００と約１００，０００との間の分子量を有する光吸収性プレポリマーであって、少なくとも一つの反応性着色剤から誘導された重合性単位と、親水性モノマー類、疎水性モノマー類およびこれらの混合物からなる群より選択されたモノマー類とを含む、光吸収性プレポリマーを含む、組成物に関するものである。 本発明の組成物は、コンタクトレンズを含む眼用装置の製造に有用である。 | ||||||
| 31 | Colored contact lens and its production | JP2000219026 | 2000-07-19 | JP2001083469A | 2001-03-30 | THAKRAR ASHOK R; OVERMYER BRADLEY K; WILLIAM E MEYERS |
| PROBLEM TO BE SOLVED: To provide a contact lens of which the colored patterns simulate the natural color structure of the human iris. SOLUTION: The contact lens is obtained by respective stages of (a) selecting an active material which is insoluble in a monomer material to be used for the hydrogel soft contact lens; (b) dispersing the active material into a carrier system which is compatible with the monomer material; (c) coating the surface of a pouring mold by using the resulted dispersion; (d) introducing a lens formable monomer liquid which contains a hydrophilic monomer capable of forming the hydrogel soft lens into the mold in such a manner that the liquid comes into contact with the coated surface; (e) polymerizing the liquid to form a lens blank impregnated with the active material into the adjacent part of the optical surface; and (f) hydrolyzing the resulted lens. COPYRIGHT: (C)2001,JPO | ||||||
| 32 | LEUCO POLYMERS AS BLUING AGENTS IN LAUNDRY CARE COMPOSITIONS | US15800689 | 2017-11-01 | US20180118945A1 | 2018-05-03 | Haihu Qin; Sanjeev K. Dey; Gregory S. Miracle |
| A leuco polymer includes a leuco monomer and an alkene. The leuco polymer has a molecular weight of at least 500 and is obtainable by polymerization of the leuco monomer and one or more alkene co-monomers. The leuco monomer consists of an alkene covalently bound to a leuco moiety and the leuco monomer has a molar extinction coefficient at a wavelength in the range 400 to 750nm of less than 1000 M−1cm−1. The alkene monomer(s) have a molar extinction coefficient at a wavelength in the range 400 to 750nm that is less than 100 M−1cm−1. Methods of making the leuco polymer, laundry care compositions comprising the leuco polymer and methods of treating textiles with such laundry care compositions. | ||||||
| 33 | REACTIVE LEUCO COMPOUNDS AND COMPOSITIONS COMPRISING THE SAME | US15800859 | 2017-11-01 | US20180118942A1 | 2018-05-03 | Sanjeev K. Dey; Wesley A. Freund; Gregory S. Miracle |
| A leuco composition comprises at least one reactive leuco compound, which reactive leuco compound comprises a leuco moiety and at least one reactive moiety covalently bound to the leuco moiety. A laundry care composition comprises a laundry care ingredient and a leuco composition. A method of treating a textile comprises the steps of (i) treating a textile with an aqueous solution containing a leuco composition, (ii) optionally, rinsing the textile, and (iii) drying the textile. | ||||||
| 34 | AQUEOUS INKJET INK COMPOSITION | US15182156 | 2016-06-14 | US20170226361A1 | 2017-08-10 | Yi-Ching LU; Iuan-Yuan WU |
| An aqueous inkjet ink composition is disclosed and includes a dye based polymeric dispersant, an aqueous organic solvent, at least one additive and water for inkjet printing specific patterns on various texture products. The dye based polymeric dispersant is present in an amount of from 2 to 30 percent by weight of the total weight of the inkjet ink composition, the aqueous organic solvent is 15 to 65 percent by weigh, and the at least one additive less than 2 percent by weigh. The dye based polymeric dispersant, the aqueous organic solvent and the at least one additive are dissolved or dispersed in water. The present invention does not easily clog at printerhead nozzles and gets rid of a great deal of industrial waste water and a tedious and complex post treatment of water cleaning, thereby scaling down the manufacturing apparatus for digital fabric. | ||||||
| 35 | Textile dyeing using nanocellulosic fibers | US14796195 | 2015-07-10 | US09506187B2 | 2016-11-29 | Sergiy Minko; Suraj Sharma; Ian Hardin; Igor Luzinov; Sandy Wu Daubenmire; Andrey Zakharchenko; Raha Saremi; Yun Sang Kim |
| Disclosed are various embodiments for dyeing a material using a dyed nanocellulose dispersion, thereby reducing or eliminating the need for water in dyeing materials, such as fabrics and textiles. A dyed nanocellulose dispersion or gel may be prepared from wood pulp fibers using a homogenizer and a dye, wherein the dyed nanocellulose dispersion comprises nanosized cellulose fibrils. The dyed nanocellulose gel may comprise an approximate concentration of 0.5% to 6%. The dyed nanocellulose dispersion may be applied to a material, such as a fabric or textile material. The fabric or textile material can be dried resulting in a dyed material. | ||||||
| 36 | POLYMERIC DYES | US12598494 | 2008-04-25 | US20100192312A1 | 2010-08-05 | Christian Cremer; Richard Lewis Riggs; Beate Frohling; Martin Muller |
| A highly crosslinked polysiloxane dye comprising at least 10 Si atoms, including at least one moiety of the formula (I) whose open Si-bonds each are linked to an oxygen atom and open O-bond is linked to a silicon atom in the rest of the polysiloxane, and wherein T is a direct bond or an organic spacer group such as C1-C18alkylene, C2-C12alkenylene, C5-C10cycloalkylene, C5-C10arylene, —C5-C10arylene-(C1-C10alkylene)- each of which may be end-capped towards the linkage to Dye by CO, COO, NR1, CONR1, NR1CONR1, CS, CSS, CSNR1, NR1CSNR1, O, S, SO, SO2, C5-C10cycloalkylene, C5-C10arylene; or T is C3-C18alkylene interrupted, and optionally end-capped towards the linkage to Dye, by CO, COO, NR1, CONR1, NR1CONR1, CS, CSS, CSNR1, NR1CSNR1, O, S, SO, —SO2—, C5-C10cycloalkylene, C5-C10arylene; or is CO; (CH2CH2—O)1-5; COO; N(R1); CON(R1); O; S; SO; SO2; R1 is hydrogen; unsubstituted or substituted, straight-chain or branched, monocyclic or polycyclic, interrupted or uninterrupted C1-C14alkyl; C2-C14alkenyl; C6-C10aryl; C6-C10aryl-C1-C10alkyl; or C5-C10alkyl(C5-C10aryl); and Dye is a residue of an organic dye, is useful for dyeing of organic materials, such as keratin-containing fibers, wool, leather, silk, cellulose or polyamides. | ||||||
| 37 | COLOURED ORGANOPOLYSILOXANES | US12304841 | 2007-06-06 | US20090209743A1 | 2009-08-20 | Roxana Barbieru; Stefan Ehrenberg; Werner Russ; Christian Ochs; Daniel Schildbach |
| The present invention relates to colored organopolysiloxanes comprising units of the formula R1a(RO)bAcR2dSiO(4-a-b-c-d)/2 (I), in which R can be identical or different and is hydrogen or a monovalent, unsubstituted or substituted hydrocarbon radical; R1 can be identical or different and is hydrogen or a monovalent, SiC-bonded, unsubstituted or substituted hydrocarbon radical; R2 can be identical or different and is a substituted monovalent hydrocarbon radical; A can be identical or different and is an organic dye radical free from sulfonic acid groups and sulfonate groups; a is 0, 1, 2 or 3; b is 0, 1, 2 or 3; d is 0, 1, 2 or 3; and c is 0, 1 or 2; with the proviso that the sum a+b+c+d is ≦3, the organopolysiloxane has at least one radical A per molecule, and in the units of the formula (I) where c is other than 0 when d is 0. The invention also relates to a process to the color organopolysiloxane. | ||||||
| 38 | Unsubstituted and polymeric lactone colorants for coloring consumer products | US12012855 | 2008-02-06 | US20080196176A1 | 2008-08-21 | Eduardo Torres; Patrick D. Moore; Joe Clark |
| This invention relates to unsubstituted and polymeric leuco colorants for use as consumer product additives to indicate a product function by color change, to make attractive or distinctive visual effects, or to provide latent or delayed color generation. The colorants may be present in a stable, colorless state and may be transformed to an intense colored state upon exposure to certain physical or chemical changes. Alternatively, the colorants may be transformed from one color to another color upon exposure to certain physical or chemical changes. The colored form of the unsubstituted or polymeric leuco colorant may be transient, since the colorant can revert back to its colorless form or its original color after the physical or chemical activation has been removed or changed. Polymeric leuco colorants are typically comprised of at least two components: at least one leuco chromophore component and at least one polymeric component. | ||||||
| 39 | Colored contact lenses and method of making same | US09986709 | 2001-11-09 | US20020027638A1 | 2002-03-07 | Ashok R. Thakrar; Bradley K. Overmyer; William E. Meyers |
| Optical lenses and methods of preparing the same, in which an active material encapsulated in resin capsules is impregnated in said lens, adjacent an optical surface thereof. The active material may be a coloring material for producing a printed color pattern in the iris or other areas of the lens, or it may be a therapeutic agent. | ||||||
| 40 | Colorant having isocyanate substituent | US25824 | 1998-02-19 | US5919846A | 1999-07-06 | Raj Batlaw; John W. Miley |
| A novel colorant compound is provided which is the addition product of an organic chromophore having at least one reactive hydroxyl or amine substituent, a polyisocyanate, and a carboxylic acid, sulfonic acid, or salt of either thereof. The polyisocyanate, added in a molar excess relative to the number of such reactive substituents, reacts with the reactive hydroxyl or amine groups to provide terminal isocyanate groups. Subsequently, the carboxylic acid or salt thereof, also added in an amount excessive in relation to the number of terminal isocyanate groups, reacts therewith to from urethane moieties on the colorant. Such a compound provides excellent ink compositions upon dilution and are very soluble within all the standard ink diluents. Furthermore, such colorants provide good jettability, waterfastness, washfastness, and the like, within ink-jet applications on various types of printing substrates. A method for producing such a colorant and specifically printed substrates colored therewith is also provided. | ||||||
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