CN104423185B - 调色剂 - Google Patents
调色剂 Download PDFInfo
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- CN104423185B CN104423185B CN201410426122.7A CN201410426122A CN104423185B CN 104423185 B CN104423185 B CN 104423185B CN 201410426122 A CN201410426122 A CN 201410426122A CN 104423185 B CN104423185 B CN 104423185B
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- dispersing agent
- toner
- pigment
- acid
- pigment dispersing
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- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
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- QMMOXUPEWRXHJS-UHFFFAOYSA-N pent-2-ene Chemical group CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 description 1
- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical class C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
- GYDSPAVLTMAXHT-UHFFFAOYSA-N pentyl 2-methylprop-2-enoate Chemical compound CCCCCOC(=O)C(C)=C GYDSPAVLTMAXHT-UHFFFAOYSA-N 0.000 description 1
- ULDDEWDFUNBUCM-UHFFFAOYSA-N pentyl prop-2-enoate Chemical compound CCCCCOC(=O)C=C ULDDEWDFUNBUCM-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
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- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- DHRLEVQXOMLTIM-UHFFFAOYSA-N phosphoric acid;trioxomolybdenum Chemical compound O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.OP(O)(O)=O DHRLEVQXOMLTIM-UHFFFAOYSA-N 0.000 description 1
- IYDGMDWEHDFVQI-UHFFFAOYSA-N phosphoric acid;trioxotungsten Chemical compound O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.OP(O)(O)=O IYDGMDWEHDFVQI-UHFFFAOYSA-N 0.000 description 1
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- IWZKICVEHNUQTL-UHFFFAOYSA-M potassium hydrogen phthalate Chemical compound [K+].OC(=O)C1=CC=CC=C1C([O-])=O IWZKICVEHNUQTL-UHFFFAOYSA-M 0.000 description 1
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 1
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- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- 238000012673 precipitation polymerization Methods 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 238000000746 purification Methods 0.000 description 1
- FYNROBRQIVCIQF-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole-5,6-dione Chemical class C1=CN=C2C(=O)C(=O)N=C21 FYNROBRQIVCIQF-UHFFFAOYSA-N 0.000 description 1
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- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
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- 239000002002 slurry Substances 0.000 description 1
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- 239000001632 sodium acetate Substances 0.000 description 1
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- FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 description 1
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- 159000000000 sodium salts Chemical class 0.000 description 1
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- UPUIQOIQVMNQAP-UHFFFAOYSA-M sodium;tetradecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCOS([O-])(=O)=O UPUIQOIQVMNQAP-UHFFFAOYSA-M 0.000 description 1
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- 125000003696 stearoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000010414 supernatant solution Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
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- 229920006250 telechelic polymer Polymers 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- RKSOPLXZQNSWAS-UHFFFAOYSA-N tert-butyl bromide Chemical compound CC(C)(C)Br RKSOPLXZQNSWAS-UHFFFAOYSA-N 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical class CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical group C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 description 1
- ZPKUAUXTKVANIS-UHFFFAOYSA-N tetradec-1-enylbenzene Chemical compound CCCCCCCCCCCCC=CC1=CC=CC=C1 ZPKUAUXTKVANIS-UHFFFAOYSA-N 0.000 description 1
- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 1
- DPUOLQHDNGRHBS-MDZDMXLPSA-N trans-Brassidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-MDZDMXLPSA-N 0.000 description 1
- YJGJRYWNNHUESM-UHFFFAOYSA-J triacetyloxystannyl acetate Chemical compound [Sn+4].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O YJGJRYWNNHUESM-UHFFFAOYSA-J 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 238000001132 ultrasonic dispersion Methods 0.000 description 1
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
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- 239000004246 zinc acetate Substances 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/087—Binders for toner particles
- G03G9/08742—Binders for toner particles comprising macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/08755—Polyesters
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/0802—Preparation methods
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- G03G9/08702—Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
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- G03G9/08708—Copolymers of styrene
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- G—PHYSICS
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- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/087—Binders for toner particles
- G03G9/08784—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775
- G03G9/08797—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775 characterised by their physical properties, e.g. viscosity, solubility, melting temperature, softening temperature, glass transition temperature
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- G—PHYSICS
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- G03G9/00—Developers
- G03G9/08—Developers with toner particles
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- G03G9/0902—Inorganic compounds
- G03G9/0904—Carbon black
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Developing Agents For Electrophotography (AREA)
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| JP2013175086 | 2013-08-26 | ||
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| KR101442439B1 (ko) * | 2010-08-24 | 2014-09-17 | 캐논 가부시끼가이샤 | 폴리에스테르, 안료 조성물, 및 토너 |
| WO2012032717A1 (ja) * | 2010-09-07 | 2012-03-15 | キヤノン株式会社 | アゾ化合物、該アゾ化合物を含有する顔料分散剤、顔料組成物、顔料分散体およびトナー |
| WO2013129696A1 (en) | 2012-02-29 | 2013-09-06 | Canon Kabushiki Kaisha | Azo compound, pigment dispersant containing the azo compound, pigment composition, pigment dispersion and toner |
| WO2015030223A1 (en) | 2013-08-28 | 2015-03-05 | Canon Kabushiki Kaisha | Novel compound, pigment dispersing agent, pigment composition, pigment dispersion and toner containing said compound |
| US9618867B2 (en) | 2015-02-20 | 2017-04-11 | Canon Kabushiki Kaisha | Pigment dispersion and toner |
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| JP2022036534A (ja) * | 2020-08-24 | 2022-03-08 | 株式会社リコー | トナー、トナー収容ユニット、画像形成装置及び画像形成方法 |
| EP4212341A4 (en) * | 2020-09-11 | 2024-03-13 | FUJIFILM Corporation | INKJET PRINTING INK AND INKJET PRINTING METHOD |
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Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002287426A (ja) * | 2001-03-27 | 2002-10-03 | Kao Corp | 電子写真用トナー |
| CN1636759A (zh) * | 2003-10-28 | 2005-07-13 | 东芝泰格有限公司 | 颜料分散体、用于紫外固化型喷墨记录的油墨前体、喷墨记录的方法、印刷品和制造颜料分散体的方法 |
| JP2007093809A (ja) * | 2005-09-27 | 2007-04-12 | Fuji Xerox Co Ltd | 静電荷像現像用トナー及び静電荷像現像用トナーの製造方法 |
| CN103048900A (zh) * | 2011-10-12 | 2013-04-17 | 佳能株式会社 | 包括具有双偶氮骨架的化合物的调色剂 |
| CN103097465A (zh) * | 2010-09-07 | 2013-05-08 | 佳能株式会社 | 偶氮化合物以及包含该偶氮化合物的颜料分散剂、颜料组合物、颜料分散体和调色剂 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3854854B2 (ja) * | 2000-11-29 | 2006-12-06 | キヤノン株式会社 | トナー及びトナーの製造方法 |
| JP3499531B2 (ja) * | 2001-01-29 | 2004-02-23 | 三洋化成工業株式会社 | 着色樹脂粒子の製造方法 |
| US6936394B2 (en) | 2001-02-28 | 2005-08-30 | Canon Kabushiki Kaisha | Replenishing developer and developing method |
| JP2007262178A (ja) * | 2006-03-28 | 2007-10-11 | Fujifilm Corp | インク組成物、インクジェット記録方法、印刷物、及び、平版印刷版の製造方法 |
| JP5392459B2 (ja) * | 2008-08-27 | 2014-01-22 | 株式会社リコー | トナー、現像剤、画像形成方法、画像形成装置、及びプロセスカートリッジ |
| JP2010160229A (ja) * | 2009-01-07 | 2010-07-22 | Canon Inc | トナー、画像形成方法、画像形成装置 |
| US8916324B2 (en) | 2010-01-20 | 2014-12-23 | Ricoh Company, Ltd. | Toner, method for producing the same, and developer |
| JP5825849B2 (ja) | 2010-06-15 | 2015-12-02 | キヤノン株式会社 | トナーの製造方法 |
| JP4999997B2 (ja) * | 2010-08-27 | 2012-08-15 | キヤノン株式会社 | アゾ化合物、該アゾ化合物を含有する顔料分散剤、顔料組成物、顔料分散体及びトナー |
| JP2012185277A (ja) * | 2011-03-04 | 2012-09-27 | Ricoh Co Ltd | 電子写真用トナー |
| JP5971985B2 (ja) | 2012-02-29 | 2016-08-17 | キヤノン株式会社 | トナーの製造方法 |
-
2014
- 2014-08-15 JP JP2014165541A patent/JP6381358B2/ja active Active
- 2014-08-21 US US14/465,722 patent/US9229345B2/en active Active
- 2014-08-25 KR KR20140110563A patent/KR20150024276A/ko not_active Abandoned
- 2014-08-25 EP EP14182099.3A patent/EP2843473B1/en active Active
- 2014-08-26 CN CN201410426122.7A patent/CN104423185B/zh active Active
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002287426A (ja) * | 2001-03-27 | 2002-10-03 | Kao Corp | 電子写真用トナー |
| CN1636759A (zh) * | 2003-10-28 | 2005-07-13 | 东芝泰格有限公司 | 颜料分散体、用于紫外固化型喷墨记录的油墨前体、喷墨记录的方法、印刷品和制造颜料分散体的方法 |
| JP2007093809A (ja) * | 2005-09-27 | 2007-04-12 | Fuji Xerox Co Ltd | 静電荷像現像用トナー及び静電荷像現像用トナーの製造方法 |
| CN103097465A (zh) * | 2010-09-07 | 2013-05-08 | 佳能株式会社 | 偶氮化合物以及包含该偶氮化合物的颜料分散剂、颜料组合物、颜料分散体和调色剂 |
| CN103048900A (zh) * | 2011-10-12 | 2013-04-17 | 佳能株式会社 | 包括具有双偶氮骨架的化合物的调色剂 |
Also Published As
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|---|---|
| EP2843473A1 (en) | 2015-03-04 |
| CN104423185A (zh) | 2015-03-18 |
| KR20150024276A (ko) | 2015-03-06 |
| US20150056549A1 (en) | 2015-02-26 |
| JP6381358B2 (ja) | 2018-08-29 |
| US9229345B2 (en) | 2016-01-05 |
| EP2843473B1 (en) | 2016-11-02 |
| JP2015064566A (ja) | 2015-04-09 |
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