DE102016109776A1 - Verfahren zum Herstellen eines härtbaren Flüssigentwicklers und härtbarer Flüssigentwickler - Google Patents
Verfahren zum Herstellen eines härtbaren Flüssigentwicklers und härtbarer Flüssigentwickler Download PDFInfo
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- DE102016109776A1 DE102016109776A1 DE102016109776.4A DE102016109776A DE102016109776A1 DE 102016109776 A1 DE102016109776 A1 DE 102016109776A1 DE 102016109776 A DE102016109776 A DE 102016109776A DE 102016109776 A1 DE102016109776 A1 DE 102016109776A1
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- Prior art keywords
- curable
- liquid developer
- pigment
- curable liquid
- binder resin
- Prior art date
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- KTPHXFUHDCWELF-UHFFFAOYSA-N n,n-dimethylhenicosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCN(C)C KTPHXFUHDCWELF-UHFFFAOYSA-N 0.000 description 1
- WCVHUIPWSPEOIG-UHFFFAOYSA-N n,n-dimethylheptadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCN(C)C WCVHUIPWSPEOIG-UHFFFAOYSA-N 0.000 description 1
- NHLUVTZJQOJKCC-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCN(C)C NHLUVTZJQOJKCC-UHFFFAOYSA-N 0.000 description 1
- PKMWMAMVKCMWQG-UHFFFAOYSA-N n,n-dimethylnonadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCN(C)C PKMWMAMVKCMWQG-UHFFFAOYSA-N 0.000 description 1
- AMAADDMFZSZCNT-UHFFFAOYSA-N n,n-dimethylnonan-1-amine Chemical compound CCCCCCCCCN(C)C AMAADDMFZSZCNT-UHFFFAOYSA-N 0.000 description 1
- PLXZCQQLUFNTPF-UHFFFAOYSA-N n,n-dimethylpentacosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCN(C)C PLXZCQQLUFNTPF-UHFFFAOYSA-N 0.000 description 1
- SNHHYQWNNZIBLN-UHFFFAOYSA-N n,n-dimethylpentadecan-1-amine Chemical compound CCCCCCCCCCCCCCCN(C)C SNHHYQWNNZIBLN-UHFFFAOYSA-N 0.000 description 1
- PFPFHPHPGFCJND-UHFFFAOYSA-N n,n-dimethyltetracosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCN(C)C PFPFHPHPGFCJND-UHFFFAOYSA-N 0.000 description 1
- SFBHPFQSSDCYSL-UHFFFAOYSA-N n,n-dimethyltetradecan-1-amine Chemical compound CCCCCCCCCCCCCCN(C)C SFBHPFQSSDCYSL-UHFFFAOYSA-N 0.000 description 1
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- ADXNPXDFKKWVGE-UHFFFAOYSA-N n,n-dimethyltridecan-1-amine Chemical compound CCCCCCCCCCCCCN(C)C ADXNPXDFKKWVGE-UHFFFAOYSA-N 0.000 description 1
- MMWFTWUMBYZIRZ-UHFFFAOYSA-N n,n-dimethylundecan-1-amine Chemical compound CCCCCCCCCCCN(C)C MMWFTWUMBYZIRZ-UHFFFAOYSA-N 0.000 description 1
- PZNXLZZWWBSQQK-UHFFFAOYSA-N n-(5-benzamido-9,10-dioxoanthracen-1-yl)benzamide Chemical compound C=1C=CC=CC=1C(=O)NC(C=1C(=O)C2=CC=C3)=CC=CC=1C(=O)C2=C3NC(=O)C1=CC=CC=C1 PZNXLZZWWBSQQK-UHFFFAOYSA-N 0.000 description 1
- UCANIZWVDIFCHH-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-7-oxobenzo[e]perimidine-4-carboxamide Chemical compound O=C1C2=CC=CC=C2C2=NC=NC3=C2C1=CC=C3C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O UCANIZWVDIFCHH-UHFFFAOYSA-N 0.000 description 1
- PCILLCXFKWDRMK-UHFFFAOYSA-N naphthalene-1,4-diol Chemical compound C1=CC=C2C(O)=CC=C(O)C2=C1 PCILLCXFKWDRMK-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- DVTHIMLUHWEZOM-UHFFFAOYSA-L nickel(2+);octanoate Chemical compound [Ni+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O DVTHIMLUHWEZOM-UHFFFAOYSA-L 0.000 description 1
- 150000002826 nitrites Chemical class 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 239000010680 novolac-type phenolic resin Substances 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
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- 235000019198 oils Nutrition 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
- 150000002921 oxetanes Chemical class 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- WEAYWASEBDOLRG-UHFFFAOYSA-N pentane-1,2,5-triol Chemical compound OCCCC(O)CO WEAYWASEBDOLRG-UHFFFAOYSA-N 0.000 description 1
- 125000005459 perfluorocyclohexyl group Chemical group 0.000 description 1
- 125000005005 perfluorohexyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- 125000005007 perfluorooctyl group Chemical group FC(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)* 0.000 description 1
- 125000005009 perfluoropropyl group Chemical group FC(C(C(F)(F)F)(F)F)(F)* 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 125000005543 phthalimide group Chemical group 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical group N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
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- 239000011148 porous material Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- VEALVRVVWBQVSL-UHFFFAOYSA-N strontium titanate Chemical compound [Sr+2].[O-][Ti]([O-])=O VEALVRVVWBQVSL-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical group O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
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- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
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- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 238000001132 ultrasonic dispersion Methods 0.000 description 1
- 238000004148 unit process Methods 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- UGCDBQWJXSAYIL-UHFFFAOYSA-N vat blue 6 Chemical compound O=C1C2=CC=CC=C2C(=O)C(C=C2Cl)=C1C1=C2NC2=C(C(=O)C=3C(=CC=CC=3)C3=O)C3=CC(Cl)=C2N1 UGCDBQWJXSAYIL-UHFFFAOYSA-N 0.000 description 1
- KJPJZBYFYBYKPK-UHFFFAOYSA-N vat yellow 1 Chemical compound C12=CC=CC=C2C(=O)C2=CC=C3N=C4C5=CC=CC=C5C(=O)C5=C4C4=C3C2=C1N=C4C=C5 KJPJZBYFYBYKPK-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 238000010947 wet-dispersion method Methods 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- GPYYEEJOMCKTPR-UHFFFAOYSA-L zinc;dodecanoate Chemical compound [Zn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O GPYYEEJOMCKTPR-UHFFFAOYSA-L 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Images
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
- G03G9/12—Developers with toner particles in liquid developer mixtures
- G03G9/13—Developers with toner particles in liquid developer mixtures characterised by polymer components
- G03G9/131—Developers with toner particles in liquid developer mixtures characterised by polymer components obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- G03G15/00—Apparatus for electrographic processes using a charge pattern
- G03G15/06—Apparatus for electrographic processes using a charge pattern for developing
- G03G15/10—Apparatus for electrographic processes using a charge pattern for developing using a liquid developer
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Liquid Developers In Electrophotography (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2015107396A JP6504917B2 (ja) | 2015-05-27 | 2015-05-27 | 硬化型液体現像剤の製造方法 |
| JP2015-107396 | 2015-05-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE102016109776A1 true DE102016109776A1 (de) | 2016-12-01 |
Family
ID=57281719
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE102016109776.4A Ceased DE102016109776A1 (de) | 2015-05-27 | 2016-05-27 | Verfahren zum Herstellen eines härtbaren Flüssigentwicklers und härtbarer Flüssigentwickler |
Country Status (3)
| Country | Link |
|---|---|
| US (2) | US9897936B2 (enExample) |
| JP (1) | JP6504917B2 (enExample) |
| DE (1) | DE102016109776A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9891547B2 (en) * | 2015-05-27 | 2018-02-13 | Canon Kabushiki Kaisha | Ultraviolet-curable liquid developer |
| US9857716B2 (en) * | 2015-05-27 | 2018-01-02 | Canon Kabushiki Kaisha | Curable liquid developer and image-forming method using curable liquid developer |
| JP6501615B2 (ja) | 2015-05-27 | 2019-04-17 | キヤノン株式会社 | 液体現像剤及び該液体現像剤の製造方法 |
| CN107710077B (zh) | 2015-05-27 | 2021-03-30 | 佳能株式会社 | 记录物质和图像形成方法 |
| US9891546B2 (en) * | 2015-05-27 | 2018-02-13 | Canon Kabushiki Kaisha | Ultraviolet-curable liquid developer |
| EP3151067A1 (en) | 2015-09-30 | 2017-04-05 | Canon Kabushiki Kaisha | Curable liquid developer |
| JP6161772B1 (ja) * | 2016-07-29 | 2017-07-12 | 東洋インキScホールディングス株式会社 | ホワイト液体現像剤及びその製造方法、またそれを用いた印刷物 |
| US20180348658A1 (en) * | 2017-05-31 | 2018-12-06 | Canon Kabushiki Kaisha | Curable liquid developer and method for producing curable liquid developer |
| US10545424B2 (en) | 2017-09-28 | 2020-01-28 | Canon Kabushiki Kaisha | Liquid developer and method of producing liquid developer |
| JP7140609B2 (ja) | 2017-09-28 | 2022-09-21 | キヤノン株式会社 | 液体現像剤及び該液体現像剤の製造方法 |
| US10423084B2 (en) | 2017-11-20 | 2019-09-24 | Canon Kabushiki Kaisha | Method for producing liquid developer |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05277800A (ja) | 1992-03-27 | 1993-10-26 | Hitachi Zosen Corp | 高速シリンダーを使用したプレス機械 |
| JP2002012607A (ja) | 2000-06-28 | 2002-01-15 | Mitsubishi Chemicals Corp | 光重合性組成物、光重合性着色組成物およびカラーフィルター |
| JP2002188025A (ja) | 2000-10-10 | 2002-07-05 | Toyo Ink Mfg Co Ltd | 活性エネルギー線硬化型インクジェットインキ |
| JP2003026978A (ja) | 1998-09-08 | 2003-01-29 | Ricoh Co Ltd | 記録液体 |
| JP3442406B2 (ja) | 1990-03-30 | 2003-09-02 | ゼロックス・コーポレーション | 硬化性液体ベヒクルを有する液体現像剤 |
| JP2003342503A (ja) | 2002-05-28 | 2003-12-03 | Konica Minolta Holdings Inc | インクジェット記録用ブラックインクおよび画像形成方法 |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2196139B (en) * | 1986-09-09 | 1990-04-04 | Fuji Photo Film Co Ltd | Liquid developer for electrostatic photography |
| US5106716A (en) * | 1989-06-14 | 1992-04-21 | Fuji Photo Film Co., Ltd. | Liquid developer for electrostatic photography |
| US5364726A (en) | 1990-03-30 | 1994-11-15 | Xerox Corporation | Liquid developers having curable liquid vehicles |
| JPH0626078A (ja) | 1992-07-03 | 1994-02-01 | Kubota Corp | バックホウ |
| US5459007A (en) * | 1994-05-26 | 1995-10-17 | Xerox Corporation | Liquid developer compositions with block copolymers |
| WO2002031066A1 (en) | 2000-10-10 | 2002-04-18 | Toyo Ink Mfg. Co., Ltd. | Actinic radiation curing jet printing ink |
| JP5175548B2 (ja) * | 2005-06-27 | 2013-04-03 | サカタインクス株式会社 | 液体現像剤の製造方法およびその製造方法により得られた液体現像剤 |
| AU2008304769B2 (en) | 2007-09-28 | 2013-10-03 | Sakata Inx Corp. | Process for producing liquid developer |
| JP5010436B2 (ja) * | 2007-11-12 | 2012-08-29 | サカタインクス株式会社 | 液体現像剤 |
| KR101251750B1 (ko) | 2008-06-02 | 2013-04-05 | 캐논 가부시끼가이샤 | 수지 미립자의 수계 분산체, 수지 미립자의 수계 분산체의 제조 방법 및 토너 입자의 제조 방법 |
| JP5277800B2 (ja) | 2008-09-03 | 2013-08-28 | セイコーエプソン株式会社 | 液体現像剤 |
| WO2010137599A1 (en) | 2009-05-28 | 2010-12-02 | Canon Kabushiki Kaisha | Toner production process and toner |
| JP5636958B2 (ja) * | 2010-12-29 | 2014-12-10 | 富士ゼロックス株式会社 | 液体現像剤、現像剤カートリッジ、画像形成方法、及び画像形成装置 |
| US8815484B2 (en) | 2011-10-12 | 2014-08-26 | Canon Kabushiki Kaisha | Toner including compound having bisazo skeleton |
| US20140377697A1 (en) | 2012-02-29 | 2014-12-25 | Canon Kabushiki Kaisha | Cyan toner containing compound having azo skeleton |
| KR20140129223A (ko) | 2012-02-29 | 2014-11-06 | 캐논 가부시끼가이샤 | 아조 골격을 갖는 화합물을 함유하는 블랙 토너 |
| KR20140129218A (ko) | 2012-02-29 | 2014-11-06 | 캐논 가부시끼가이샤 | 아조 골격을 갖는 화합물을 함유하는 마젠타 토너 |
| US9057970B2 (en) | 2012-03-09 | 2015-06-16 | Canon Kabushiki Kaisha | Method for producing core-shell structured resin microparticles and core-shell structured toner containing core-shell structured resin microparticles |
| KR20130126482A (ko) | 2012-05-10 | 2013-11-20 | 캐논 가부시끼가이샤 | 토너 및 토너 제조 방법 |
| AU2014215195B2 (en) * | 2013-02-08 | 2017-07-27 | Sakata Inx Corporation | Liquid developing agent |
| JP6381358B2 (ja) | 2013-08-26 | 2018-08-29 | キヤノン株式会社 | トナー |
| CA2931057C (en) | 2013-11-28 | 2018-06-19 | Canon Kabushiki Kaisha | Ultraviolet-curable liquid developer |
| US9715187B2 (en) | 2014-04-01 | 2017-07-25 | Canon Kabushiki Kaisha | Method of producing a compound having a colorant structure, and toner containing a compound obtained by the production method |
| US9556290B2 (en) | 2014-04-01 | 2017-01-31 | Canon Kabushiki Kaisha | Method for producing compound having colorant structure at main chain terminal of polymer, and pigment dispersant, pigment composition, pigment dispersion and toner containing compound obtained by the production method |
-
2015
- 2015-05-27 JP JP2015107396A patent/JP6504917B2/ja not_active Expired - Fee Related
-
2016
- 2016-05-27 US US15/166,633 patent/US9897936B2/en not_active Expired - Fee Related
- 2016-05-27 DE DE102016109776.4A patent/DE102016109776A1/de not_active Ceased
-
2018
- 2018-01-23 US US15/877,887 patent/US20180210362A1/en not_active Abandoned
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3442406B2 (ja) | 1990-03-30 | 2003-09-02 | ゼロックス・コーポレーション | 硬化性液体ベヒクルを有する液体現像剤 |
| JPH05277800A (ja) | 1992-03-27 | 1993-10-26 | Hitachi Zosen Corp | 高速シリンダーを使用したプレス機械 |
| JP2003026978A (ja) | 1998-09-08 | 2003-01-29 | Ricoh Co Ltd | 記録液体 |
| JP2002012607A (ja) | 2000-06-28 | 2002-01-15 | Mitsubishi Chemicals Corp | 光重合性組成物、光重合性着色組成物およびカラーフィルター |
| JP2002188025A (ja) | 2000-10-10 | 2002-07-05 | Toyo Ink Mfg Co Ltd | 活性エネルギー線硬化型インクジェットインキ |
| JP2003342503A (ja) | 2002-05-28 | 2003-12-03 | Konica Minolta Holdings Inc | インクジェット記録用ブラックインクおよび画像形成方法 |
Non-Patent Citations (3)
| Title |
|---|
| "Organic Pigments", W. Herbst und K. Hunger |
| Coating Basics and Engineering (Seite 53, Yuji Harasaki, Converting Technical Institute) |
| JIS K 0070 |
Also Published As
| Publication number | Publication date |
|---|---|
| US9897936B2 (en) | 2018-02-20 |
| JP2016224102A (ja) | 2016-12-28 |
| JP6504917B2 (ja) | 2019-04-24 |
| US20160349652A1 (en) | 2016-12-01 |
| US20180210362A1 (en) | 2018-07-26 |
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