CA2705983C - Solid or phase change inks with improved properties - Google Patents
Solid or phase change inks with improved properties Download PDFInfo
- Publication number
- CA2705983C CA2705983C CA 2705983 CA2705983A CA2705983C CA 2705983 C CA2705983 C CA 2705983C CA 2705983 CA2705983 CA 2705983 CA 2705983 A CA2705983 A CA 2705983A CA 2705983 C CA2705983 C CA 2705983C
- Authority
- CA
- Canada
- Prior art keywords
- ink
- wax
- composition
- ink composition
- polar
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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- 239000007787 solid Substances 0.000 title claims abstract description 60
- 230000008859 change Effects 0.000 title claims abstract description 52
- 239000000976 ink Substances 0.000 title claims description 256
- 239000001993 wax Substances 0.000 claims abstract description 155
- 230000002378 acidificating effect Effects 0.000 claims abstract description 31
- 239000000654 additive Substances 0.000 claims abstract description 15
- 230000000996 additive effect Effects 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims description 128
- 239000002253 acid Substances 0.000 claims description 68
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- -1 paraffins Substances 0.000 claims description 34
- 239000000463 material Substances 0.000 claims description 30
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- 238000002844 melting Methods 0.000 claims description 26
- 230000008018 melting Effects 0.000 claims description 26
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- 239000011347 resin Substances 0.000 claims description 10
- 125000001931 aliphatic group Chemical group 0.000 claims description 8
- 229920001577 copolymer Polymers 0.000 claims description 8
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- FUSNPOOETKRESL-ZPHPHTNESA-N (z)-n-octadecyldocos-13-enamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)CCCCCCCCCCC\C=C/CCCCCCCC FUSNPOOETKRESL-ZPHPHTNESA-N 0.000 description 4
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 4
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- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 4
- VOWAEIGWURALJQ-UHFFFAOYSA-N Dicyclohexyl phthalate Chemical compound C=1C=CC=C(C(=O)OC2CCCCC2)C=1C(=O)OC1CCCCC1 VOWAEIGWURALJQ-UHFFFAOYSA-N 0.000 description 3
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- 238000013461 design Methods 0.000 description 3
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- RDYMFSUJUZBWLH-UHFFFAOYSA-N endosulfan Chemical compound C12COS(=O)OCC2C2(Cl)C(Cl)=C(Cl)C1(Cl)C2(Cl)Cl RDYMFSUJUZBWLH-UHFFFAOYSA-N 0.000 description 3
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 3
- 238000005227 gel permeation chromatography Methods 0.000 description 3
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 3
- 150000003949 imides Chemical class 0.000 description 3
- 230000001965 increasing effect Effects 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 3
- FATBGEAMYMYZAF-UHFFFAOYSA-N oleicacidamide-heptaglycolether Natural products CCCCCCCCC=CCCCCCCCC(N)=O FATBGEAMYMYZAF-UHFFFAOYSA-N 0.000 description 3
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- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
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- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- TXWSZJSDZKWQAU-UHFFFAOYSA-N 2,9-dimethyl-5,12-dihydroquinolino[2,3-b]acridine-7,14-dione Chemical compound N1C2=CC=C(C)C=C2C(=O)C2=C1C=C(C(=O)C=1C(=CC=C(C=1)C)N1)C1=C2 TXWSZJSDZKWQAU-UHFFFAOYSA-N 0.000 description 2
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- CGLVZFOCZLHKOH-UHFFFAOYSA-N 8,18-dichloro-5,15-diethyl-5,15-dihydrodiindolo(3,2-b:3',2'-m)triphenodioxazine Chemical compound CCN1C2=CC=CC=C2C2=C1C=C1OC3=C(Cl)C4=NC(C=C5C6=CC=CC=C6N(C5=C5)CC)=C5OC4=C(Cl)C3=NC1=C2 CGLVZFOCZLHKOH-UHFFFAOYSA-N 0.000 description 2
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- VTHAYUPMFCMKIH-UHFFFAOYSA-N 1-heptylsulfonylheptane Chemical compound CCCCCCCS(=O)(=O)CCCCCCC VTHAYUPMFCMKIH-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/34—Hot-melt inks
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/12—Printing inks based on waxes or bitumen
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Ink Jet (AREA)
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| US12/482,096 | 2009-06-10 | ||
| US12/482,096 US8915993B2 (en) | 2009-06-10 | 2009-06-10 | Solid or phase change inks with improved properties |
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| CA2705983A1 CA2705983A1 (en) | 2010-12-10 |
| CA2705983C true CA2705983C (en) | 2013-04-23 |
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| CA 2705983 Expired - Fee Related CA2705983C (en) | 2009-06-10 | 2010-06-03 | Solid or phase change inks with improved properties |
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| EP (1) | EP2261291A1 (enExample) |
| JP (2) | JP2010285617A (enExample) |
| KR (1) | KR101438861B1 (enExample) |
| CN (1) | CN101921506A (enExample) |
| CA (1) | CA2705983C (enExample) |
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| ATE516693T1 (de) * | 2008-11-04 | 2011-07-15 | Rohm & Haas Elect Mat | Verbesserte schmelzzusammensetzungen |
| US8915993B2 (en) * | 2009-06-10 | 2014-12-23 | Xerox Corporation | Solid or phase change inks with improved properties |
| US8303832B2 (en) * | 2009-08-17 | 2012-11-06 | Palo Alto Research Center Incorporated | Solid inks for masks for printed circuit boards and other electronic devices |
| US8273166B2 (en) * | 2011-01-18 | 2012-09-25 | Xerox Corporation | Phase change ink compositions and colorants for use in the same |
| US8459788B2 (en) * | 2011-03-04 | 2013-06-11 | Xerox Corporation | Curable solid ink compositions comprising novel curable wax |
| US8500260B2 (en) | 2011-04-27 | 2013-08-06 | Xerox Corporation | Ink compositions incorporating substituted oxazoline compounds or substituted oxazoline derivatives |
| US8460447B2 (en) | 2011-04-27 | 2013-06-11 | Xerox Corporation | Substituted oxazoline compounds or substituted oxazoline derivatives |
| US20140071213A1 (en) * | 2012-09-13 | 2014-03-13 | Xerox Corporation | Phase Change Ink Compositions For Image Robustness |
| US8851648B2 (en) * | 2012-09-18 | 2014-10-07 | Xerox Corporation | Blends of semi-crystalline materials for inks for direct-to-paper printing |
| US9453139B2 (en) | 2013-08-20 | 2016-09-27 | Rohm And Haas Electronic Materials Llc | Hot melt compositions with improved etch resistance |
| US9228102B2 (en) | 2014-04-03 | 2016-01-05 | Xerox Corporation | Scratch resistant inks |
| US9481803B2 (en) * | 2014-12-13 | 2016-11-01 | Xerox Corporation | Water dispersible phase change ink suitable for use as a photo-mask |
| US11732146B2 (en) | 2016-10-10 | 2023-08-22 | Hewlett-Packard Development Company, L.P. | Liquid ink containing polytetrafluoroethylene wax emulsion |
| CN108219842A (zh) * | 2018-01-30 | 2018-06-29 | 公安县瑞凯高分子材料股份有限公司 | 酰胺蜡改性微粉化费托蜡及其制备方法和应用 |
| US11143958B2 (en) * | 2018-04-04 | 2021-10-12 | Xerox Corporation | Method for applying curable gellant composition for digital embossing and other raised print applications |
| CN109516623B (zh) * | 2018-11-16 | 2021-06-01 | 浙江万盛股份有限公司 | 一种三丁氧乙基磷酸酯废水的综合利用方法 |
Family Cites Families (92)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE755392A (fr) * | 1969-08-28 | 1971-02-01 | Teletype Corp | Encre et appareil d'impression electrostatique |
| JPS5657848A (en) | 1979-10-17 | 1981-05-20 | Hodogaya Chem Co Ltd | Preparation of triarylmethane dye |
| US4390369A (en) * | 1981-12-17 | 1983-06-28 | Exxon Research And Engineering Co. | Natural wax-containing ink jet inks |
| US4484948A (en) * | 1981-12-17 | 1984-11-27 | Exxon Research And Engineering Co. | Natural wax-containing ink jet inks |
| EP0167247B1 (en) * | 1984-05-10 | 1990-08-08 | Willett International Limited | Method for applying thermoplastic inks to a substrate and a composition for use therein |
| US4658064A (en) * | 1984-08-27 | 1987-04-14 | Milliken Research Corporation | P-formyl-N,N-dipolyoxyalkylenesubstitutedaniline |
| JPS61101574A (ja) * | 1984-10-23 | 1986-05-20 | Ricoh Co Ltd | 水性インク |
| EP0187352B1 (en) | 1984-12-31 | 1991-06-05 | Howtek, Inc. | A method of ink jet colour printing |
| DE3671460D1 (de) | 1985-06-25 | 1990-06-28 | Howtek Inc | Tinte fuer den tintenstrahldruck. |
| JPS6354476A (ja) * | 1986-08-25 | 1988-03-08 | Seiko Epson Corp | 熱溶融性インク |
| US5194638A (en) * | 1987-09-18 | 1993-03-16 | Union Camp Corporation | Resinous binders for use in ink compositions for ink jet printing |
| US4830671A (en) * | 1987-09-18 | 1989-05-16 | Union Camp Corporation | Ink compositions for ink jet printing |
| US4889560A (en) * | 1988-08-03 | 1989-12-26 | Tektronix, Inc. | Phase change ink composition and phase change ink produced therefrom |
| US4889761A (en) * | 1988-08-25 | 1989-12-26 | Tektronix, Inc. | Substrates having a light-transmissive phase change ink printed thereon and methods for producing same |
| DE3842014A1 (de) * | 1988-12-14 | 1990-06-21 | Bayer Ag | Verfahren zur herstellung von sulfogruppenfreien triphenylmethanfarbstoffen |
| US5151120A (en) * | 1989-03-31 | 1992-09-29 | Hewlett-Packard Company | Solid ink compositions for thermal ink-jet printing having improved printing characteristics |
| US5006170A (en) * | 1989-06-22 | 1991-04-09 | Xerox Corporation | Hot melt ink compositions |
| US5122187A (en) * | 1989-06-22 | 1992-06-16 | Xerox Corporation | Hot melt ink compositions |
| GB2238792A (en) | 1989-09-07 | 1991-06-12 | Coates Brothers Plc | Polyamides |
| US5221335A (en) * | 1990-05-23 | 1993-06-22 | Coates Electrographics Limited | Stabilized pigmented hot melt ink containing nitrogen-modified acrylate polymer as dispersion-stabilizer agent |
| JPH04370167A (ja) | 1991-06-19 | 1992-12-22 | Fujicopian Co Ltd | プリンター用固形インク組成物 |
| EP0502200A4 (en) * | 1990-08-30 | 1993-07-07 | Fujicopian Co., Ltd. | Printer ink composition and printing medium prepared therefrom |
| US5156675A (en) * | 1991-05-16 | 1992-10-20 | Xerox Corporation | Ink for ink jet printing |
| US5259874A (en) * | 1991-10-23 | 1993-11-09 | Hewlett-Packard Company | Solid ink compositions suitable for use in color transparencies |
| DE4205636C2 (de) | 1992-02-25 | 1994-12-22 | Siegwerk Druckfarben Gmbh & Co | Tief- und Flachdruckverfahren und Druckmaschinen zur Durchführung der Verfahren |
| DE4205713C2 (de) | 1992-02-25 | 1994-08-04 | Siegwerk Druckfarben Gmbh & Co | Druckfarbe, Verfahren zu ihrer Herstellung und deren Verwendung |
| JPH0641482A (ja) * | 1992-07-21 | 1994-02-15 | Canon Inc | インクジェット記録用インク、常温固体のインク及びそれを用いたインクジェット記録方法 |
| US5385957A (en) | 1992-08-24 | 1995-01-31 | Videojet Systems International, Inc. | Hotmelt ink jet comprising ionomers having melting points from about 50° C. to about 130° or a softening point below about 80° C., and an image-forming agent |
| US5621022A (en) * | 1992-11-25 | 1997-04-15 | Tektronix, Inc. | Use of polymeric dyes in hot melt ink jet inks |
| US5372852A (en) * | 1992-11-25 | 1994-12-13 | Tektronix, Inc. | Indirect printing process for applying selective phase change ink compositions to substrates |
| US5389958A (en) * | 1992-11-25 | 1995-02-14 | Tektronix, Inc. | Imaging process |
| GB9226772D0 (en) | 1992-12-23 | 1993-02-17 | Coates Brothers Plc | Hot melt ink jet printing |
| GB2280905A (en) | 1993-08-06 | 1995-02-15 | Coates Brothers Plc | Ethylenically unsaturated photoinitiator |
| US5597856A (en) * | 1993-09-24 | 1997-01-28 | Dataproducts Corporation | Hot melt ink for transparency applications |
| GB2290793B (en) * | 1994-06-20 | 1998-05-06 | Cray Valley Ltd | Powder coating compositions |
| GB2294939A (en) | 1994-11-08 | 1996-05-15 | Coates Brothers Plc | Hot melt ink jet printing composition comprising an oligourea |
| JPH08245915A (ja) * | 1995-03-09 | 1996-09-24 | Riso Kagaku Corp | 孔版印刷用エマルジョンインク |
| JPH093377A (ja) | 1995-06-23 | 1997-01-07 | Hitachi Koki Co Ltd | インクジェット用ホットメルト型インク組成物 |
| JPH0971743A (ja) | 1995-09-08 | 1997-03-18 | Hitachi Koki Co Ltd | インクジェット用インク組成物とその記録方法 |
| GB2305670A (en) | 1995-09-27 | 1997-04-16 | Coates Brothers Plc | Hot melt ink jet vehicles |
| FR2739418B1 (fr) | 1995-10-02 | 1997-12-19 | Poclain Hydraulics Sa | Moteur hydraulique d'assistance |
| GB2305928A (en) | 1995-10-06 | 1997-04-23 | Coates Brothers Plc | Coloured hot melt ink jet vehicle |
| JP2007070637A (ja) * | 1996-02-14 | 2007-03-22 | Union Camp Corp | ホットメルトインクの処方に有用な重合脂肪酸のジエステル |
| GB9605399D0 (en) | 1996-03-14 | 1996-05-15 | Coates Brothers Plc | Hot melt ink composition |
| US5780528A (en) * | 1996-06-28 | 1998-07-14 | Tektronix, Inc. | Isocyanate-derived colored resins for use in phase change ink jet inks |
| US5830942A (en) * | 1996-06-28 | 1998-11-03 | Tektronix, Inc. | Phase change ink formulation using a urethane and urethane/urea isocyanate-derived resins |
| US5827918A (en) * | 1996-06-28 | 1998-10-27 | Tektronix, Inc. | Phase change ink formulation using urea and urethane isocyanate-derived resins |
| US5782966A (en) * | 1996-06-28 | 1998-07-21 | Tektronix, Inc. | Isocyanate-derived materials for use in phase change ink jet inks |
| US5783658A (en) * | 1996-06-28 | 1998-07-21 | Tektronix, Inc. | Phase change ink formulation using a urethane isocyanate-derived resin and a urethane isocyanate-derived wax |
| US5750604A (en) * | 1996-06-28 | 1998-05-12 | Tektronix, Inc. | Phase change ink formulation using a urethane isocyanate-derived resin |
| US5919839A (en) * | 1996-06-28 | 1999-07-06 | Tektronix, Inc. | Phase change ink formulation using an isocyanate-derived wax and a clear ink carrier base |
| JPH10316912A (ja) | 1997-05-15 | 1998-12-02 | Brother Ind Ltd | 熱溶融固体インク |
| JPH1121485A (ja) * | 1997-07-04 | 1999-01-26 | Hitachi Koki Co Ltd | インクジェット用ホットメルト型インク組成物 |
| JP3729310B2 (ja) * | 1997-08-01 | 2005-12-21 | リコープリンティングシステムズ株式会社 | インクジェット用ホットメルト型インク組成物 |
| US6015847A (en) * | 1998-02-13 | 2000-01-18 | Tektronix, Inc. | Magenta phase change ink formulation containing organic sulfonic acid |
| US5989325A (en) * | 1998-03-05 | 1999-11-23 | Xerox Corporation | Ink compositions |
| US5948150A (en) * | 1998-05-05 | 1999-09-07 | Hewlett-Packard Company | Composition to improve colorfastness of a printed image |
| US6689837B1 (en) * | 1998-06-17 | 2004-02-10 | Meadwestvaco Corporation | Hybrid polymers for phase change ink jet inks |
| US6312121B1 (en) * | 1998-09-11 | 2001-11-06 | Xerox Corporation | Ink jet printing process |
| JP4174870B2 (ja) * | 1998-09-25 | 2008-11-05 | コニカミノルタホールディングス株式会社 | トナー |
| JP4280953B2 (ja) * | 1998-09-25 | 2009-06-17 | Ｄｉｃ株式会社 | 静電荷像現像用トナー組成物及び現像剤 |
| JP2000191964A (ja) * | 1998-12-25 | 2000-07-11 | Hitachi Koki Co Ltd | インクジェット用ホットメルト型インク組成物及びその記録方法 |
| US6174937B1 (en) * | 1999-07-16 | 2001-01-16 | Xerox Corporation | Composition of matter, a phase change ink, and a method of reducing a coefficient of friction of a phase change ink formulation |
| US6309453B1 (en) * | 1999-09-20 | 2001-10-30 | Xerox Corporation | Colorless compounds, solid inks, and printing methods |
| US6602594B2 (en) * | 2000-04-25 | 2003-08-05 | Nichiyu Giken Kogyo Co., Ltd. | Irreversible heat-sensitive composition |
| JP4714331B2 (ja) * | 2000-10-30 | 2011-06-29 | トッパン・フォームズ株式会社 | バックカーボンインキを用いた改ざん防止用感圧複写シート |
| JP5121101B2 (ja) * | 2001-04-27 | 2013-01-16 | キヤノン株式会社 | 顔料インクおよびその製造方法 |
| JP2003026963A (ja) | 2001-07-11 | 2003-01-29 | Seiren Co Ltd | ホットメルトインク組成物及びそれによる記録物 |
| US6906118B2 (en) * | 2001-09-07 | 2005-06-14 | Xerox Corporation | Phase change ink compositions |
| US6652635B2 (en) * | 2001-09-07 | 2003-11-25 | Xerox Corporation | Cyan phase change inks |
| US8003725B2 (en) * | 2002-08-12 | 2011-08-23 | Exxonmobil Chemical Patents Inc. | Plasticized hetero-phase polyolefin blends |
| FR2853657B1 (fr) * | 2003-04-10 | 2005-06-24 | Centre Nat Rech Scient | Macromolecules auto assemblees et photopolymerisees autour de nanotubes de carbone, un procede pour leur preparation, et leurs applications |
| US7034185B2 (en) * | 2003-04-24 | 2006-04-25 | Xerox Corporation | Colorant precursor compositions |
| US7094812B2 (en) | 2003-04-24 | 2006-08-22 | Xerox Corporations | Colorant compositions |
| US6860930B2 (en) * | 2003-06-25 | 2005-03-01 | Xerox Corporation | Phase change inks containing branched triamides |
| US6860931B2 (en) | 2003-06-26 | 2005-03-01 | Xerox Corporation | Phase change inks containing colorant compounds |
| US6998493B2 (en) | 2003-06-26 | 2006-02-14 | Xerox Corporation | Colorant compounds |
| US6835238B1 (en) * | 2003-06-26 | 2004-12-28 | Xerox Corporation | Phase change inks containing colorant compounds |
| EP1687382B1 (en) * | 2003-10-27 | 2007-04-04 | HRD Corp | Novel wax for reducing mar and abrasion in inks and coatings |
| US6858070B1 (en) | 2003-11-25 | 2005-02-22 | Xerox Corporation | Phase change inks |
| US7347892B2 (en) | 2004-08-13 | 2008-03-25 | Xerox Corporation | Phase change inks containing modified pigment particles |
| US7270408B2 (en) * | 2005-01-14 | 2007-09-18 | Xerox Corporation | Low level cure transfuse assist for printing with radiation curable ink |
| US20070095250A1 (en) * | 2005-10-28 | 2007-05-03 | Uhlir-Tsang Linda C | Ink Compositions and Methods for Improving Neutrality, Hue Angle and/or Media Independence |
| US7501015B2 (en) * | 2005-11-30 | 2009-03-10 | Xerox Corporation | Phase change inks |
| US7578587B2 (en) * | 2005-11-30 | 2009-08-25 | Xerox Corporation | Curable overcoat for wax-based inks |
| US7311768B2 (en) * | 2005-11-30 | 2007-12-25 | Xerox Corporation | Phase change inks containing Fischer-Tropsch waxes |
| US20080098927A1 (en) | 2006-10-26 | 2008-05-01 | Xerox Corporation | Pigmented phase change inks |
| US20080098929A1 (en) * | 2006-10-26 | 2008-05-01 | Xerox Corporation | Phase change inks |
| US7677713B2 (en) * | 2007-05-30 | 2010-03-16 | Xerox Corporation | Solid ink set incorporating naturally derived materials and processes thereof |
| AU2008280231B9 (en) | 2007-07-20 | 2013-06-27 | Sicpa Holding Sa | Intaglio printing inks |
| US7812064B2 (en) | 2007-08-07 | 2010-10-12 | Xerox Corporation | Phase change ink compositions |
| US8915993B2 (en) * | 2009-06-10 | 2014-12-23 | Xerox Corporation | Solid or phase change inks with improved properties |
-
2009
- 2009-06-10 US US12/482,096 patent/US8915993B2/en not_active Expired - Fee Related
-
2010
- 2010-06-01 EP EP10164539A patent/EP2261291A1/en not_active Ceased
- 2010-06-03 CA CA 2705983 patent/CA2705983C/en not_active Expired - Fee Related
- 2010-06-03 JP JP2010127511A patent/JP2010285617A/ja active Pending
- 2010-06-09 CN CN2010101992561A patent/CN101921506A/zh active Pending
- 2010-06-09 KR KR20100054380A patent/KR101438861B1/ko not_active Expired - Fee Related
-
2012
- 2012-05-18 US US13/475,737 patent/US20120227621A1/en not_active Abandoned
-
2014
- 2014-07-03 JP JP2014137529A patent/JP5997211B2/ja not_active Expired - Fee Related
- 2014-07-30 US US14/446,997 patent/US20140338563A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CA2705983A1 (en) | 2010-12-10 |
| US20100313788A1 (en) | 2010-12-16 |
| JP2010285617A (ja) | 2010-12-24 |
| KR20100132924A (ko) | 2010-12-20 |
| EP2261291A1 (en) | 2010-12-15 |
| US20140338563A1 (en) | 2014-11-20 |
| JP5997211B2 (ja) | 2016-09-28 |
| CN101921506A (zh) | 2010-12-22 |
| KR101438861B1 (ko) | 2014-09-16 |
| US8915993B2 (en) | 2014-12-23 |
| US20120227621A1 (en) | 2012-09-13 |
| JP2014177655A (ja) | 2014-09-25 |
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| Date | Code | Title | Description |
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| EEER | Examination request | ||
| MKLA | Lapsed |
Effective date: 20190603 |