MX2012004768A - Composiciones de tinta solida que comprenden mezclas cristalinas - amorfas. - Google Patents
Composiciones de tinta solida que comprenden mezclas cristalinas - amorfas.Info
- Publication number
- MX2012004768A MX2012004768A MX2012004768A MX2012004768A MX2012004768A MX 2012004768 A MX2012004768 A MX 2012004768A MX 2012004768 A MX2012004768 A MX 2012004768A MX 2012004768 A MX2012004768 A MX 2012004768A MX 2012004768 A MX2012004768 A MX 2012004768A
- Authority
- MX
- Mexico
- Prior art keywords
- phase change
- cps
- viscosity
- change ink
- ink
- Prior art date
Links
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Classifications
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- 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
- C09D11/50—Sympathetic, colour changing or similar inks
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- 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
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- 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
- C09D11/38—Inkjet printing inks characterised by non-macromolecular additives other than solvents, pigments or dyes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M2205/00—Printing methods or features related to printing methods; Location or type of the layers
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- 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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13/095,636 US8506040B2 (en) | 2011-04-27 | 2011-04-27 | Solid ink compositions comprising crystalline-amorphous mixtures |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2012004768A true MX2012004768A (es) | 2013-03-15 |
Family
ID=47007861
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2012004768A MX2012004768A (es) | 2011-04-27 | 2012-04-23 | Composiciones de tinta solida que comprenden mezclas cristalinas - amorfas. |
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| US (1) | US8506040B2 (enExample) |
| JP (1) | JP5795543B2 (enExample) |
| KR (1) | KR101751549B1 (enExample) |
| CN (1) | CN102757682B (enExample) |
| BR (1) | BR102012009839A2 (enExample) |
| CA (1) | CA2775183C (enExample) |
| DE (1) | DE102012205872B4 (enExample) |
| MX (1) | MX2012004768A (enExample) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9499709B2 (en) | 2010-03-01 | 2016-11-22 | Xerox Corporation | Oligomeric rosin esters for use in inks |
| US8308859B1 (en) * | 2011-04-27 | 2012-11-13 | Xerox Corporation | Phase change ink components and methods of making the same |
| US8833917B2 (en) * | 2011-04-27 | 2014-09-16 | Xerox Corporation | Solid ink compositions comprising crystalline-amorphous mixtures |
| US8647424B2 (en) * | 2012-04-26 | 2014-02-11 | Xerox Corporation | Phase change inks comprising inorganic nucleating agents |
| US8882897B2 (en) | 2012-04-26 | 2014-11-11 | Xerox Corporation | Phase change inks comprising aromatic diester crystalline compounds |
| US8888905B2 (en) | 2012-04-26 | 2014-11-18 | Xerox Corporation | Fast crystallizing crystalline-amorphous ink compositions and methods for making the same |
| US8647423B2 (en) * | 2012-04-26 | 2014-02-11 | Xerox Corporation | Phase change inks comprising fatty acids |
| US8741040B2 (en) * | 2012-04-26 | 2014-06-03 | Xerox Corporation | Phase change ink compositions comprising aromatic ethers |
| US9528016B2 (en) | 2012-04-26 | 2016-12-27 | Xerox Corporation | Phase change inks comprising crystalline amides |
| US8741043B2 (en) * | 2012-04-26 | 2014-06-03 | Xerox Corporation | Bio-renewable fast crystallizing phase change inks |
| US8784547B2 (en) * | 2012-06-18 | 2014-07-22 | Xerox Corporation | Lightfast solid ink compositions |
| US8741042B2 (en) | 2012-10-28 | 2014-06-03 | Xerox Corporation | Phase change inks comprising linear primary alcohols |
| US8758494B2 (en) | 2012-11-19 | 2014-06-24 | Xerox Corporation | Pigmented magenta and yellow phase change inks |
| US9062226B2 (en) | 2012-11-19 | 2015-06-23 | Xerox Corporation | Compositions of pigment concentrates in phase change inks |
| US8753441B2 (en) | 2012-11-19 | 2014-06-17 | Xerox Corporation | Bio-renewable phase change inks comprising recycled resin materials |
| US8591640B1 (en) * | 2012-11-19 | 2013-11-26 | Xerox Corporation | Bio-renewable fast crystallizing phase change inks |
| US8827393B2 (en) * | 2013-01-16 | 2014-09-09 | Xerox Corporation | Fluorescent phase change ink compositions |
| US9109131B2 (en) * | 2013-01-16 | 2015-08-18 | Xerox Corporation | Photochromic phase change ink compositions |
| US8778070B1 (en) | 2013-02-13 | 2014-07-15 | Xerox Corporation | Ink composition and method of jetting ink |
| US9187663B2 (en) | 2013-03-21 | 2015-11-17 | Xerox Corporation | Ink composition and method of jetting ink |
| US9090791B2 (en) * | 2013-06-04 | 2015-07-28 | Xerox Corporation | Mixtures of ester of tartaric acid and ester of citric acid as amorphous materials for phase change inks |
| US9168776B2 (en) * | 2013-06-17 | 2015-10-27 | Xerox Corporation | Method of increasing ink crystallization |
| US9193883B2 (en) | 2013-06-18 | 2015-11-24 | Xerox Corporation | Phase change ink containing polyester for improved image robustness |
| US9096768B2 (en) | 2013-08-15 | 2015-08-04 | Xerox Corporation | Curable phase change ink compositions |
| US9228097B2 (en) * | 2013-08-28 | 2016-01-05 | Xerox Corporation | Phase change inks |
| US9074104B2 (en) * | 2013-09-04 | 2015-07-07 | Xerox Corporation | Inks comprising amorphous ureas |
| US9447297B2 (en) | 2013-10-14 | 2016-09-20 | Xerox Corporation | Phase change ink containing amorphous amides |
| US9011587B1 (en) * | 2013-10-14 | 2015-04-21 | Xerox Corporation | Phase change inks comprising novel crystalline compounds |
| US9227922B2 (en) | 2013-10-14 | 2016-01-05 | Xerox Corporation | Amorphous amides |
| US9120943B2 (en) | 2013-10-15 | 2015-09-01 | Xerox Corporation | Bio-renewable phase change inks |
| US9422440B2 (en) | 2013-12-06 | 2016-08-23 | Xerox Corporation | Bis-ureas as amorphous materials for phase-change ink |
| US20150283758A1 (en) | 2014-04-08 | 2015-10-08 | Xerox Corporation | Method of making three-dimensional objects using crystalline and amorphous compounds |
| US20150283759A1 (en) | 2014-04-08 | 2015-10-08 | Xerox Corporation | Method of making three-dimensional objects using bio-renewable crystalline-amorphous materials |
Family Cites Families (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4490731A (en) | 1982-11-22 | 1984-12-25 | Hewlett-Packard Company | Ink dispenser with "frozen" solid ink |
| 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 |
| US5195430A (en) | 1989-05-24 | 1993-03-23 | Tektronix, Inc. | Dual roller apparatus for pressure fixing sheet material |
| US5231135A (en) | 1989-09-05 | 1993-07-27 | Milliken Research Corporation | Lightfast colored polymeric coatings and process for making same |
| 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 |
| 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 |
| US5621022A (en) | 1992-11-25 | 1997-04-15 | Tektronix, Inc. | Use of polymeric dyes in hot melt ink jet inks |
| NL1005174C2 (nl) | 1997-02-04 | 1998-08-06 | Oce Tech Bv | Inktsamenstelling voor een smeltbare inkt. |
| NL1009791C2 (nl) | 1998-08-03 | 2000-02-04 | Oce Tech Bv | Inktsamenstelling voor een smeltbare inkt. |
| US6221137B1 (en) | 1999-06-18 | 2001-04-24 | Xerox Corporation | Metal phthalocyanine colorants for phase change inks |
| NL1012549C2 (nl) | 1999-07-09 | 2001-01-10 | Ocu Technologies B V | Inktsamenstelling voor een smeltbare inkt en een werkwijze voor het bedrukken van een substraat met een dergelijke inktsamenstelling. |
| NL1017049C2 (nl) | 2001-01-08 | 2002-07-09 | Ocu Technologies B V | Inktsamenstelling voor een smeltbare inkt. |
| US6476219B1 (en) | 2002-02-08 | 2002-11-05 | Xerox Corporation | Methods for preparing phthalocyanine compositions |
| US6726755B2 (en) | 2002-02-08 | 2004-04-27 | Xerox Corporation | Ink compositions containing phthalocyanines |
| US6472523B1 (en) | 2002-02-08 | 2002-10-29 | Xerox Corporation | Phthalocyanine compositions |
| NL1020682C2 (nl) | 2002-05-27 | 2003-11-28 | Oce Tech Bv | Smeltbare inktsamenstelling. |
| US6646111B1 (en) | 2002-06-27 | 2003-11-11 | Xerox Corporation | Dimeric azo pyridone colorants |
| US6696552B2 (en) | 2002-06-27 | 2004-02-24 | Xerox Corporation | Process for preparing substituted pyridone compounds |
| US6755902B2 (en) | 2002-06-27 | 2004-06-29 | Xerox Corporation | Phase change inks containing azo pyridone colorants |
| US6590082B1 (en) | 2002-06-27 | 2003-07-08 | Xerox Corporation | Azo pyridone colorants |
| US6713614B2 (en) | 2002-06-27 | 2004-03-30 | Xerox Corporation | Dimeric azo pyridone colorants |
| US6576748B1 (en) | 2002-06-27 | 2003-06-10 | Xerox Corporation | Method for making dimeric azo pyridone colorants |
| US6673139B1 (en) | 2002-06-27 | 2004-01-06 | Xerox Corporation | Phase change inks containing dimeric azo pyridone colorants |
| US6576747B1 (en) | 2002-06-27 | 2003-06-10 | Xerox Corporation | Processes for preparing dianthranilate compounds and diazopyridone colorants |
| US6663703B1 (en) | 2002-06-27 | 2003-12-16 | Xerox Corporation | Phase change inks containing dimeric azo pyridone colorants |
| US7053227B2 (en) | 2002-09-27 | 2006-05-30 | Xerox Corporation | Methods for making colorant compounds |
| US6958406B2 (en) | 2002-09-27 | 2005-10-25 | Xerox Corporation | Colorant compounds |
| US6821327B2 (en) | 2002-09-27 | 2004-11-23 | Xerox Corporation | Phase change inks |
| US20080098927A1 (en) | 2006-10-26 | 2008-05-01 | Xerox Corporation | Pigmented phase change inks |
| US7381831B1 (en) | 2007-04-04 | 2008-06-03 | Xerox Corporation | Colorant compounds |
| US7427323B1 (en) | 2007-06-07 | 2008-09-23 | Xerox Corporation | Quinacridone nanoscale pigment particles |
| US20090223409A1 (en) * | 2008-03-07 | 2009-09-10 | Xerox Corporation | Compounds suitable for use in inks and inks having such compounds |
| US20100122642A1 (en) * | 2008-11-17 | 2010-05-20 | Xerox Corporation | Inks including carbon nanotubes dispersed in a polymer matrix |
| CN101525405B (zh) * | 2009-04-07 | 2011-05-25 | 北京高盟新材料股份有限公司 | 醇溶型油墨用树脂的制备方法及应用 |
-
2011
- 2011-04-27 US US13/095,636 patent/US8506040B2/en active Active
-
2012
- 2012-03-07 JP JP2012050601A patent/JP5795543B2/ja not_active Expired - Fee Related
- 2012-04-11 DE DE102012205872.9A patent/DE102012205872B4/de not_active Expired - Fee Related
- 2012-04-20 CA CA2775183A patent/CA2775183C/en not_active Expired - Fee Related
- 2012-04-23 MX MX2012004768A patent/MX2012004768A/es active IP Right Grant
- 2012-04-25 KR KR1020120043428A patent/KR101751549B1/ko not_active Expired - Fee Related
- 2012-04-26 CN CN201210126462.9A patent/CN102757682B/zh not_active Expired - Fee Related
- 2012-04-26 BR BR102012009839-3A patent/BR102012009839A2/pt not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| KR20120121847A (ko) | 2012-11-06 |
| DE102012205872A1 (de) | 2012-10-31 |
| BR102012009839A2 (pt) | 2014-01-14 |
| US20120274699A1 (en) | 2012-11-01 |
| CA2775183C (en) | 2016-07-05 |
| JP5795543B2 (ja) | 2015-10-14 |
| DE102012205872B4 (de) | 2018-02-22 |
| US8506040B2 (en) | 2013-08-13 |
| KR101751549B1 (ko) | 2017-06-27 |
| CN102757682B (zh) | 2015-04-22 |
| RU2012117421A (ru) | 2013-11-10 |
| CA2775183A1 (en) | 2012-10-27 |
| CN102757682A (zh) | 2012-10-31 |
| JP2012233154A (ja) | 2012-11-29 |
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