JP5311726B2 - インクキャリア、インクキャリアを含む相変化インク、およびインクキャリアの製造方法 - Google Patents
インクキャリア、インクキャリアを含む相変化インク、およびインクキャリアの製造方法 Download PDFInfo
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- JP5311726B2 JP5311726B2 JP2006190805A JP2006190805A JP5311726B2 JP 5311726 B2 JP5311726 B2 JP 5311726B2 JP 2006190805 A JP2006190805 A JP 2006190805A JP 2006190805 A JP2006190805 A JP 2006190805A JP 5311726 B2 JP5311726 B2 JP 5311726B2
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- RJLZSKYNYLYCNY-UHFFFAOYSA-N ethyl carbamate;isocyanic acid Chemical compound N=C=O.CCOC(N)=O RJLZSKYNYLYCNY-UHFFFAOYSA-N 0.000 description 1
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- ILXYDRFJSVKZLV-UHFFFAOYSA-N oxosulfamic acid Chemical compound OS(=O)(=O)N=O ILXYDRFJSVKZLV-UHFFFAOYSA-N 0.000 description 1
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- 239000000843 powder Substances 0.000 description 1
- CSPHPKQCLCBONW-UHFFFAOYSA-N pyridin-1-ium-1-carbonitrile Chemical compound N#C[N+]1=CC=CC=C1 CSPHPKQCLCBONW-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
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- 125000003011 styrenyl group Chemical class [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
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- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 description 1
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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 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
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/181632 | 2005-07-13 | ||
| US11/181,632 US7563313B2 (en) | 2005-07-13 | 2005-07-13 | Ink carriers, phase change inks including same and methods for making same |
Publications (3)
| Publication Number | Publication Date |
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| JP2007023278A JP2007023278A (ja) | 2007-02-01 |
| JP2007023278A5 JP2007023278A5 (enExample) | 2009-08-27 |
| JP5311726B2 true JP5311726B2 (ja) | 2013-10-09 |
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Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7572325B2 (en) * | 2005-11-30 | 2009-08-11 | Xerox Corporation | Ink carriers, phase change inks including same and methods for making same |
| US7714040B2 (en) | 2005-11-30 | 2010-05-11 | Xerox Corporation | Phase change inks containing curable amide gellant compounds |
| KR101621575B1 (ko) * | 2008-10-10 | 2016-05-16 | 다우 글로벌 테크놀로지스 엘엘씨 | 종이계 기재용 다층 코팅 |
| US9005484B2 (en) * | 2009-03-31 | 2015-04-14 | Xerox Corporation | Low polarity nano silver gels |
| US8853293B2 (en) * | 2009-12-18 | 2014-10-07 | Xerox Corporation | Curable solid ink compositions |
| US20110152396A1 (en) * | 2009-12-18 | 2011-06-23 | Xerox Corporation | Curable Solid Overcoat Compositions |
| US8507584B2 (en) | 2010-04-22 | 2013-08-13 | Xerox Corporation | Phase change inks containing amide gellant compounds with aromatic end groups |
| US8084637B2 (en) | 2010-04-22 | 2011-12-27 | Xerox Corporation | Amide gellant compounds with aromatic end groups |
| US8449095B2 (en) | 2010-07-13 | 2013-05-28 | Xerox Corporation | Radiation curable solid ink compositions suitable for transfuse printing applications |
| US9109124B2 (en) * | 2011-06-01 | 2015-08-18 | Xerox Corporation | Solid ink compositions comprising semicrystalline oligomer resins |
| CN103214808B (zh) * | 2012-01-18 | 2016-12-14 | 柯尼卡美能达商用科技株式会社 | 使用含再生pc和再生pet无卤阻燃树脂组合物的复印机或打印机的外装部件 |
| US8702221B2 (en) * | 2012-05-08 | 2014-04-22 | Xerox Corporation | Gellant compositions with aromatic end-caps and oligomeric molecular weight distributions |
| US20140071213A1 (en) * | 2012-09-13 | 2014-03-13 | Xerox Corporation | Phase Change Ink Compositions For Image Robustness |
| US9447297B2 (en) * | 2013-10-14 | 2016-09-20 | Xerox Corporation | Phase change ink containing amorphous amides |
| US10696857B2 (en) | 2017-12-14 | 2020-06-30 | Xerox Corporation | Curable gellant ink |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5194638A (en) * | 1987-09-18 | 1993-03-16 | Union Camp Corporation | Resinous binders for use in 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 |
| 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 |
| US5084099A (en) * | 1991-06-17 | 1992-01-28 | Tektronix, Inc. | Phase change ink colorants and phase change inks produced therefrom |
| DE4205713C2 (de) | 1992-02-25 | 1994-08-04 | Siegwerk Druckfarben Gmbh & Co | Druckfarbe, Verfahren zu ihrer Herstellung und deren Verwendung |
| DE4205636C2 (de) | 1992-02-25 | 1994-12-22 | Siegwerk Druckfarben Gmbh & Co | Tief- und Flachdruckverfahren und Druckmaschinen zur Durchführung der Verfahren |
| 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 |
| US5455326A (en) * | 1994-09-28 | 1995-10-03 | Union Camp Corporation | Ink-jet printing compositions |
| US5545504A (en) * | 1994-10-03 | 1996-08-13 | Xerox Corporation | Ink jettable toner compositions and processes for making and using |
| US5783657A (en) | 1996-10-18 | 1998-07-21 | Union Camp Corporation | Ester-terminated polyamides of polymerized fatty acids useful in formulating transparent gels in low polarity liquids |
| US5863319A (en) * | 1996-12-10 | 1999-01-26 | Markem Corporation | Thermally stable hot melt ink |
| JP2002538259A (ja) * | 1999-03-03 | 2002-11-12 | イーストマン ケミカル カンパニー | ポリアミド／エマルジョンポリマーブレンド |
| US6350889B1 (en) * | 1999-06-24 | 2002-02-26 | Arizona Chemical Company | Ink jet printing compositions containing ester-terminated dimer acid-based oligo (ester/amide) |
| 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. |
| 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 |
| US6838535B2 (en) * | 2001-03-23 | 2005-01-04 | University Of Pennsylvania | Process for the living radical polymerization of chlorine containing monomers |
| US6821327B2 (en) * | 2002-09-27 | 2004-11-23 | Xerox Corporation | Phase change inks |
-
2005
- 2005-07-13 US US11/181,632 patent/US7563313B2/en not_active Expired - Fee Related
-
2006
- 2006-07-11 JP JP2006190805A patent/JP5311726B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20070012217A1 (en) | 2007-01-18 |
| JP2007023278A (ja) | 2007-02-01 |
| US7563313B2 (en) | 2009-07-21 |
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