JP2007521418A - プラスチック物品の染色方法 - Google Patents
プラスチック物品の染色方法 Download PDFInfo
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- JP2007521418A JP2007521418A JP2006543898A JP2006543898A JP2007521418A JP 2007521418 A JP2007521418 A JP 2007521418A JP 2006543898 A JP2006543898 A JP 2006543898A JP 2006543898 A JP2006543898 A JP 2006543898A JP 2007521418 A JP2007521418 A JP 2007521418A
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- dye
- dyebath
- diol
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- thermoplastic
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 42
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- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims abstract description 15
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- ITPCCQOGYMDBHK-UHFFFAOYSA-N 3h-benzo[f][1,2]benzoxazine;2,3-dihydro-1h-indole Chemical compound C1=CC=C2NCCC2=C1.C1=CC=CC2=C(C=CNO3)C3=CC=C21 ITPCCQOGYMDBHK-UHFFFAOYSA-N 0.000 claims description 2
- VCMLCMCXCRBSQO-UHFFFAOYSA-N 3h-benzo[f]chromene Chemical compound C1=CC=CC2=C(C=CCO3)C3=CC=C21 VCMLCMCXCRBSQO-UHFFFAOYSA-N 0.000 claims description 2
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- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/60—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing polyethers
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/16—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using dispersed, e.g. acetate, dyestuffs
- D06P1/18—Azo dyes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/16—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using dispersed, e.g. acetate, dyestuffs
- D06P1/20—Anthraquinone dyes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/60—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing polyethers
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/64—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
- D06P1/651—Compounds without nitrogen
- D06P1/65106—Oxygen-containing compounds
- D06P1/65118—Compounds containing hydroxyl groups
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Coloring (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/733,111 US7175675B2 (en) | 2003-12-11 | 2003-12-11 | Method of dyeing a plastic article |
| PCT/US2004/040544 WO2005061780A1 (en) | 2003-12-11 | 2004-12-06 | Method of dyeing a plastic article |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007521418A true JP2007521418A (ja) | 2007-08-02 |
| JP2007521418A5 JP2007521418A5 (enExample) | 2008-01-31 |
Family
ID=34653025
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006543898A Withdrawn JP2007521418A (ja) | 2003-12-11 | 2004-12-06 | プラスチック物品の染色方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7175675B2 (enExample) |
| EP (1) | EP1694904A1 (enExample) |
| JP (1) | JP2007521418A (enExample) |
| KR (1) | KR20060121169A (enExample) |
| CN (1) | CN100503962C (enExample) |
| CA (1) | CA2549150A1 (enExample) |
| WO (1) | WO2005061780A1 (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009091578A (ja) * | 2007-10-09 | 2009-04-30 | Bayer Material Science Llc | プラスチック物品を色味付ける方法 |
| JP2016511046A (ja) * | 2013-03-08 | 2016-04-14 | ナイキ イノヴェイト シーヴィー | 多色物体の作製方法 |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1239583C (zh) * | 2001-02-21 | 2006-02-01 | 东丽株式会社 | 聚苯硫醚构件及其制造方法 |
| US20070079453A1 (en) * | 2003-12-11 | 2007-04-12 | Bayer Materialscience Llc | Method of dyeing a semi-finished product |
| EP1739119A1 (en) * | 2005-06-29 | 2007-01-03 | Bayer MaterialScience AG | Process for the treatment of plastic profiles |
| WO2007052468A1 (ja) * | 2005-11-01 | 2007-05-10 | Nikon Corporation | フォトクロミック染料によるボディ部材の装飾方法およびフォトクロミック装飾されたボディ部材並びにボディ部材用基材 |
| US20070259117A1 (en) * | 2006-05-04 | 2007-11-08 | Bayer Materialscience Llc | Article having photochromic properties and process for its manufacture |
| US8206463B2 (en) * | 2006-05-04 | 2012-06-26 | Bayer Materialscience Llc | Colored article of manufacture and a process for its preparation |
| US20070259118A1 (en) * | 2006-05-04 | 2007-11-08 | Bayer Materialscience Llc | Method of treating a plastic article |
| US20080067124A1 (en) * | 2006-09-19 | 2008-03-20 | Kaczkowski Edward F | Solvent recovery system for plastic dying operation |
| FR2907113A1 (fr) * | 2006-10-16 | 2008-04-18 | Chemoptics Sarl | Procede de traitement de verre organique |
| US20090297829A1 (en) * | 2008-06-02 | 2009-12-03 | Bayer Materialscience Llc | Process for incorporating metal nanoparticles in a polymeric article and articles made therewith |
| WO2014047620A1 (en) | 2012-09-24 | 2014-03-27 | RADCO Infusion Technologies, LLC | Removal of color from thermoplastics |
| US8758860B1 (en) | 2012-11-07 | 2014-06-24 | Bayer Materialscience Llc | Process for incorporating an ion-conducting polymer into a polymeric article to achieve anti-static behavior |
| US9668538B2 (en) | 2013-03-08 | 2017-06-06 | Nike, Inc. | System and method for coloring articles |
| US9974362B2 (en) | 2013-03-08 | 2018-05-22 | NIKE, Inc.. | Assembly for coloring articles and method of coloring |
| US10302267B2 (en) | 2014-10-27 | 2019-05-28 | Ford Global Technologies, Llc | Color infused automobile headlamp lens |
| SG11201808168TA (en) * | 2016-03-29 | 2018-10-30 | Covestro Deutschland Ag | Method for the partial coloring of plastic parts |
| CN105880135B (zh) * | 2016-04-08 | 2018-06-15 | 广东欧珀移动通信有限公司 | 移动终端、移动终端壳体及壳体染色方法 |
| EP3452232A1 (en) | 2016-05-06 | 2019-03-13 | Radco Infusion Technologies, LLC | Continuous linear substrate infusion |
| US9718080B1 (en) | 2016-05-06 | 2017-08-01 | RADCO Infusion Technologies, LLC | Linear substrate infusion compartment |
| CN108841033A (zh) * | 2016-05-19 | 2018-11-20 | 晋江国盛新材料科技有限公司 | 一种用染色tpu发泡珠粒制成成型体的方法 |
| CN113026382A (zh) * | 2021-02-22 | 2021-06-25 | 苏州图延模具有限公司 | 一种cnc加工pmma透明件的上色技术 |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1619473A1 (de) | 1966-05-17 | 1971-03-11 | Bayer Ag | Verfahren zum Faerben von Gebilden aus aromatischen Polycarbonaten |
| US3630664A (en) | 1967-06-07 | 1971-12-28 | Bayer Ag | Process for dyeing shaped articles of aromatic polycarbonates |
| AT282072B (de) * | 1968-05-30 | 1970-06-10 | Therachemie Chem Therapeut | Haarfärbemittel |
| US3514246A (en) | 1969-07-11 | 1970-05-26 | American Aniline Prod | Method of dyeing shaped polycarbonate resins |
| US4465728A (en) | 1972-09-25 | 1984-08-14 | H.L.H. Corp. | Dye decorated plastic articles |
| JPS5031179A (enExample) | 1973-07-24 | 1975-03-27 | ||
| US4003699A (en) * | 1974-11-22 | 1977-01-18 | Henkel & Cie G.M.B.H. | Oxidation hair dyes based upon tetraaminopyrimidine developers |
| JPS5110875A (en) | 1974-07-17 | 1976-01-28 | Seiko Instr & Electronics | Goseijushino chakushokuho |
| JPS5159254A (enExample) | 1974-11-20 | 1976-05-24 | Matsushita Electric Industrial Co Ltd | |
| JPS5517156A (en) | 1978-07-25 | 1980-02-06 | Fujikura Ltd | Connector of optical fiber |
| JPS565358A (en) | 1979-06-21 | 1981-01-20 | Nippon Sheet Glass Co Ltd | Manufacture of colored fog-resistent product |
| JPS5631085A (en) | 1979-08-17 | 1981-03-28 | Seiko Instr & Electronics | Coloring of polycarbonate resin |
| US4812142A (en) | 1987-12-01 | 1989-03-14 | Burlington Industries, Inc. | Colored polycarbonate articles with high impact resistance |
| DE3843892A1 (de) * | 1988-12-24 | 1990-06-28 | Wella Ag | Oxidationshaarfaerbemittel mit einem gehalt an diaminopyrazolderivaten und neue diaminopyrazolderivate |
| US5205862A (en) | 1989-10-26 | 1993-04-27 | Kabushiki Kaisha Pilot | Water resistant ink compositions and process for preparation |
| JPH0457977A (ja) | 1990-06-20 | 1992-02-25 | Showa Denko Kk | プラスチックレンズの染色方法 |
| DE4133957A1 (de) * | 1991-10-14 | 1993-04-15 | Wella Ag | Haarfaerbemittel mit einem gehalt an aminopyrazolderivaten sowie neue pyrazolderivate |
| IL105147A0 (en) * | 1992-09-11 | 1993-07-08 | American Optical Corp | Production of photochromic plastic lenses |
| US5258444A (en) | 1993-01-22 | 1993-11-02 | Ppg Industries, Inc. | Aqueous coating composition for plastic substrates |
| US5453100A (en) | 1994-06-14 | 1995-09-26 | General Electric Company | Method for color dyeing polycarbonate |
| FR2733749B1 (fr) * | 1995-05-05 | 1997-06-13 | Oreal | Compositions pour la teinture des fibres keratiniques contenant des diamino pyrazoles, procede de teinture, nouveaux diamino pyrazoles et leur procede de preparation |
| DE19543988A1 (de) * | 1995-11-25 | 1997-05-28 | Wella Ag | Oxidationshaarfärbemittel mit einem Gehalt an 3,4,5-Triaminopyrazolderivaten sowie neue 3,4,5-Triaminopyrazolderivate |
| FR2750048B1 (fr) * | 1996-06-21 | 1998-08-14 | Oreal | Compositions de teinture des fibres keratiniques contenant des derives pyrazolo-(1, 5-a)-pyrimidine, procede de teinture, nouveaux derives pyrazolo-(1, 5-a)-pyrimidine et leur procede de preparation |
| JPH1148609A (ja) | 1997-08-04 | 1999-02-23 | Fuji Xerox Co Ltd | 画像記録方法及び画像記録装置 |
| FR2769219B1 (fr) * | 1997-10-03 | 2000-03-10 | Oreal | Composition oxydante et utilisations pour la teinture, pour la deformation permanente ou pour la decoloration des fibres keratiniques |
| GB9817235D0 (en) | 1998-08-08 | 1998-10-07 | Zeneca Ltd | Compound,composition and use |
| CA2246505A1 (en) | 1998-09-03 | 2000-03-03 | Christophe U. Ryser | Method for tinting tint-able plastic material using microwave energy |
| JP2000248476A (ja) | 1999-03-03 | 2000-09-12 | Kenji Murakami | ポリカーボネート樹脂を染色によって堅牢度良く着色する方法 |
| US6749646B2 (en) | 2001-11-07 | 2004-06-15 | Bayer Polymers Llc | Dip-dyeable polycarbonate process |
| US6733543B2 (en) * | 2002-03-26 | 2004-05-11 | Bayer Polymers Llc | Process for making dyed articles |
| US6994735B2 (en) * | 2003-05-08 | 2006-02-07 | Bayer Materialscience Llc | Process for tinting plastic articles |
-
2003
- 2003-12-11 US US10/733,111 patent/US7175675B2/en not_active Expired - Lifetime
-
2004
- 2004-12-06 WO PCT/US2004/040544 patent/WO2005061780A1/en not_active Ceased
- 2004-12-06 KR KR1020067011414A patent/KR20060121169A/ko not_active Ceased
- 2004-12-06 JP JP2006543898A patent/JP2007521418A/ja not_active Withdrawn
- 2004-12-06 CN CNB2004800371152A patent/CN100503962C/zh not_active Expired - Fee Related
- 2004-12-06 EP EP04812961A patent/EP1694904A1/en not_active Withdrawn
- 2004-12-06 CA CA002549150A patent/CA2549150A1/en not_active Abandoned
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009091578A (ja) * | 2007-10-09 | 2009-04-30 | Bayer Material Science Llc | プラスチック物品を色味付ける方法 |
| JP2016511046A (ja) * | 2013-03-08 | 2016-04-14 | ナイキ イノヴェイト シーヴィー | 多色物体の作製方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2549150A1 (en) | 2005-07-07 |
| US20050125916A1 (en) | 2005-06-16 |
| HK1095368A1 (zh) | 2007-05-04 |
| EP1694904A1 (en) | 2006-08-30 |
| WO2005061780A1 (en) | 2005-07-07 |
| US7175675B2 (en) | 2007-02-13 |
| CN1894464A (zh) | 2007-01-10 |
| CN100503962C (zh) | 2009-06-24 |
| KR20060121169A (ko) | 2006-11-28 |
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