CN102757680B - 相变油墨 - Google Patents
相变油墨 Download PDFInfo
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- CN102757680B CN102757680B CN201210129795.7A CN201210129795A CN102757680B CN 102757680 B CN102757680 B CN 102757680B CN 201210129795 A CN201210129795 A CN 201210129795A CN 102757680 B CN102757680 B CN 102757680B
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- SLUKQUGVTITNSY-UHFFFAOYSA-N 2,6-di-tert-butyl-4-methoxyphenol Chemical compound COC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SLUKQUGVTITNSY-UHFFFAOYSA-N 0.000 description 1
- IIKSFQIOFHBWSO-UHFFFAOYSA-N 2,9-bis(2-phenylethyl)anthra(2,1,9-def:6,5,10-d'e'f')diisoquinoline-1,3,8,10(2h,9h)-tetrone Chemical compound O=C1C(C2=C34)=CC=C3C(C=35)=CC=C(C(N(CCC=6C=CC=CC=6)C6=O)=O)C5=C6C=CC=3C4=CC=C2C(=O)N1CCC1=CC=CC=C1 IIKSFQIOFHBWSO-UHFFFAOYSA-N 0.000 description 1
- FBRJYBGLCHWYOE-UHFFFAOYSA-N 2-(trifluoromethyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(F)(F)F FBRJYBGLCHWYOE-UHFFFAOYSA-N 0.000 description 1
- MFYSUUPKMDJYPF-UHFFFAOYSA-N 2-[(4-methyl-2-nitrophenyl)diazenyl]-3-oxo-n-phenylbutanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C(=O)C)N=NC1=CC=C(C)C=C1[N+]([O-])=O MFYSUUPKMDJYPF-UHFFFAOYSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical group CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- PUNNQKXGKNOLTB-UHFFFAOYSA-N 2-[[2-[2-[2-[[1,3-dioxo-1-[(2-oxo-1,3-dihydrobenzimidazol-5-yl)amino]butan-2-yl]diazenyl]phenoxy]ethoxy]phenyl]diazenyl]-3-oxo-n-(2-oxo-1,3-dihydrobenzimidazol-5-yl)butanamide Chemical compound C1=C2NC(=O)NC2=CC(NC(=O)C(N=NC=2C(=CC=CC=2)OCCOC=2C(=CC=CC=2)N=NC(C(C)=O)C(=O)NC=2C=C3NC(=O)NC3=CC=2)C(=O)C)=C1 PUNNQKXGKNOLTB-UHFFFAOYSA-N 0.000 description 1
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- MIBXCSXTQNGTKN-UHFFFAOYSA-N CCCCP(CCCC)(CCCC)(O)O.N Chemical compound CCCCP(CCCC)(CCCC)(O)O.N MIBXCSXTQNGTKN-UHFFFAOYSA-N 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 239000004150 EU approved colour Substances 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- OKOBUGCCXMIKDM-UHFFFAOYSA-N Irganox 1098 Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)NCCCCCCNC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 OKOBUGCCXMIKDM-UHFFFAOYSA-N 0.000 description 1
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- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- YCUVUDODLRLVIC-UHFFFAOYSA-N Sudan black B Chemical compound C1=CC(=C23)NC(C)(C)NC2=CC=CC3=C1N=NC(C1=CC=CC=C11)=CC=C1N=NC1=CC=CC=C1 YCUVUDODLRLVIC-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
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- 150000001298 alcohols Chemical class 0.000 description 1
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- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- POJOORKDYOPQLS-UHFFFAOYSA-L barium(2+) 5-chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-methylbenzenesulfonate Chemical compound [Ba+2].C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O.C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O POJOORKDYOPQLS-UHFFFAOYSA-L 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- VDQQXEISLMTGAB-UHFFFAOYSA-N chloramine T Chemical compound [Na+].CC1=CC=C(S(=O)(=O)[N-]Cl)C=C1 VDQQXEISLMTGAB-UHFFFAOYSA-N 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000009795 derivation Methods 0.000 description 1
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical group 0.000 description 1
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 1
- SUXCALIDMIIJCK-UHFFFAOYSA-L disodium;4-amino-3-[[4-[4-[(1-amino-4-sulfonatonaphthalen-2-yl)diazenyl]-3-methylphenyl]-2-methylphenyl]diazenyl]naphthalene-1-sulfonate Chemical compound [Na+].[Na+].C1=CC=CC2=C(N)C(N=NC3=CC=C(C=C3C)C=3C=C(C(=CC=3)N=NC=3C(=C4C=CC=CC4=C(C=3)S([O-])(=O)=O)N)C)=CC(S([O-])(=O)=O)=C21 SUXCALIDMIIJCK-UHFFFAOYSA-L 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000005686 electrostatic field Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- HQIXACMMBRHSSY-UHFFFAOYSA-N fluorophosphonous acid Chemical compound OP(O)F HQIXACMMBRHSSY-UHFFFAOYSA-N 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000001261 hydroxy acids Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 230000003116 impacting effect Effects 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Natural products OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000003760 magnetic stirring Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- WNWZKKBGFYKSGA-UHFFFAOYSA-N n-(4-chloro-2,5-dimethoxyphenyl)-2-[[2,5-dimethoxy-4-(phenylsulfamoyl)phenyl]diazenyl]-3-oxobutanamide Chemical compound C1=C(Cl)C(OC)=CC(NC(=O)C(N=NC=2C(=CC(=C(OC)C=2)S(=O)(=O)NC=2C=CC=CC=2)OC)C(C)=O)=C1OC WNWZKKBGFYKSGA-UHFFFAOYSA-N 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
- 239000012782 phase change material Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 230000003678 scratch resistant effect Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
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- 230000007704 transition Effects 0.000 description 1
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- IMFACGCPASFAPR-UHFFFAOYSA-O tributylazanium Chemical compound CCCC[NH+](CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-O 0.000 description 1
- DKBXPLYSDKSFEQ-UHFFFAOYSA-L turquoise gll Chemical compound [Na+].[Na+].[Cu+2].N1=C(N=C2[N-]3)[C]4C(S(=O)(=O)[O-])=CC=CC4=C1N=C([N-]1)C4=CC=CC(S([O-])(=O)=O)=C4C1=NC(C=1C4=CC=CC=1)=NC4=NC3=C1[C]2C=CC=C1 DKBXPLYSDKSFEQ-UHFFFAOYSA-L 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
- C09D11/38—Inkjet printing inks characterised by non-macromolecular additives other than solvents, pigments or dyes
-
- 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 |
|---|---|---|---|
| US13/095,028 US8840232B2 (en) | 2011-04-27 | 2011-04-27 | Phase change ink |
| US13/095028 | 2011-04-27 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102757680A CN102757680A (zh) | 2012-10-31 |
| CN102757680B true CN102757680B (zh) | 2015-05-20 |
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|---|---|---|---|
| CN201210129795.7A Expired - Fee Related CN102757680B (zh) | 2011-04-27 | 2012-04-27 | 相变油墨 |
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|---|---|
| US (1) | US8840232B2 (enExample) |
| JP (1) | JP5865163B2 (enExample) |
| CN (1) | CN102757680B (enExample) |
| CA (1) | CA2775198C (enExample) |
| DE (1) | DE102012206027B4 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8690309B2 (en) * | 2011-04-27 | 2014-04-08 | Xerox Corporation | Print process for phase separation ink |
| US8308859B1 (en) | 2011-04-27 | 2012-11-13 | Xerox Corporation | Phase change ink components and methods of making the same |
| US8784547B2 (en) * | 2012-06-18 | 2014-07-22 | Xerox Corporation | Lightfast solid ink compositions |
| US8747536B1 (en) | 2013-01-31 | 2014-06-10 | Xerox Corporation | Phase change ink formulation including malic acid derivatives as amorphous materials |
| US9139743B2 (en) | 2013-01-31 | 2015-09-22 | Xerox Corporation | Malic acid derivatives as amorphous materials for phase change ink |
| US9011587B1 (en) * | 2013-10-14 | 2015-04-21 | Xerox Corporation | Phase change inks comprising novel crystalline compounds |
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| US6306203B1 (en) * | 1999-09-23 | 2001-10-23 | Xerox Corporation | Phase change inks |
| CN1637085A (zh) * | 2003-11-25 | 2005-07-13 | 施乐公司 | 制备相变型油墨的方法 |
| CN101495579A (zh) * | 2006-08-01 | 2009-07-29 | 奥西-技术有限公司 | 热熔性油墨 |
| CN101684216A (zh) * | 2008-09-23 | 2010-03-31 | 施乐公司 | 含低粘度官能化蜡的油墨载体,含该载体的相变油墨,及制备方法 |
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| US7271284B2 (en) | 2005-11-30 | 2007-09-18 | Xerox Corporation | Process for making curable amide gellant compounds |
| JP4983103B2 (ja) * | 2006-06-06 | 2012-07-25 | 大日本印刷株式会社 | カラーフィルター用インクジェットインク及びその製造方法、カラーフィルターの製造方法、並びに液晶表示装置の製造方法 |
| 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 |
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| DE102010009379B4 (de) * | 2010-02-26 | 2014-10-30 | Carl Zeiss Vision International Gmbh | Druckfarbenzusammensetzung, Verfahren zum Bedrucken und Verwendung der Druckfarbenzusammensetzung |
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2011
- 2011-04-27 US US13/095,028 patent/US8840232B2/en not_active Expired - Fee Related
-
2012
- 2012-04-10 JP JP2012089156A patent/JP5865163B2/ja not_active Expired - Fee Related
- 2012-04-13 DE DE102012206027.8A patent/DE102012206027B4/de not_active Expired - Fee Related
- 2012-04-20 CA CA2775198A patent/CA2775198C/en not_active Expired - Fee Related
- 2012-04-27 CN CN201210129795.7A patent/CN102757680B/zh not_active Expired - Fee Related
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| US6306203B1 (en) * | 1999-09-23 | 2001-10-23 | Xerox Corporation | Phase change inks |
| CN1637085A (zh) * | 2003-11-25 | 2005-07-13 | 施乐公司 | 制备相变型油墨的方法 |
| CN101495579A (zh) * | 2006-08-01 | 2009-07-29 | 奥西-技术有限公司 | 热熔性油墨 |
| CN101684216A (zh) * | 2008-09-23 | 2010-03-31 | 施乐公司 | 含低粘度官能化蜡的油墨载体,含该载体的相变油墨,及制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| US8840232B2 (en) | 2014-09-23 |
| DE102012206027A1 (de) | 2012-10-31 |
| JP5865163B2 (ja) | 2016-02-17 |
| US20120274698A1 (en) | 2012-11-01 |
| CA2775198C (en) | 2015-06-30 |
| CA2775198A1 (en) | 2012-10-27 |
| DE102012206027B4 (de) | 2020-08-13 |
| CN102757680A (zh) | 2012-10-31 |
| JP2012233173A (ja) | 2012-11-29 |
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