CN102053511B - 电子照相感光构件、处理盒和电子照相设备 - Google Patents
电子照相感光构件、处理盒和电子照相设备 Download PDFInfo
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- CN102053511B CN102053511B CN2009101784000A CN200910178400A CN102053511B CN 102053511 B CN102053511 B CN 102053511B CN 2009101784000 A CN2009101784000 A CN 2009101784000A CN 200910178400 A CN200910178400 A CN 200910178400A CN 102053511 B CN102053511 B CN 102053511B
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| JP4940370B2 (ja) | 2010-06-29 | 2012-05-30 | キヤノン株式会社 | 電子写真感光体、プロセスカートリッジおよび電子写真装置 |
| JP4958995B2 (ja) | 2010-08-27 | 2012-06-20 | キヤノン株式会社 | 電子写真感光体、プロセスカートリッジ及び電子写真装置 |
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| WO2016156535A1 (en) * | 2015-03-31 | 2016-10-06 | Sony Corporation | N and p active materials for organic photoelectric conversion layers in organic photodiodes |
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| JP2025052783A (ja) | 2023-09-25 | 2025-04-07 | 富士フイルムビジネスイノベーション株式会社 | 電子写真感光体、プロセスカートリッジ及び画像形成装置 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5677097A (en) * | 1996-01-18 | 1997-10-14 | Fuji Xerox Co., Ltd. | Electrophotographic photoreceptor |
| US5815776A (en) * | 1994-11-22 | 1998-09-29 | Fuji Xerox Co., Ltd. | Electrophotographic apparatus with photoreceptor having undercoat layer, containing an electronic transporting pigment and reactive organometallic compound |
Family Cites Families (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4082551A (en) * | 1977-03-31 | 1978-04-04 | Eastman Kodak Company | Electrophotographic element containing a multilayer interlayer |
| US4418117A (en) * | 1981-02-18 | 1983-11-29 | Allied Paper Incorporated | Conductive barrier coat for electrostatic masters |
| JPS5968753A (ja) * | 1982-10-13 | 1984-04-18 | Fuji Photo Film Co Ltd | 電子写真製版材料用支持体 |
| US4442193A (en) | 1983-02-22 | 1984-04-10 | Eastman Kodak Company | Photoconductive compositions and elements containing naphthalene bis-dicarboximide compounds |
| JPS59171963A (ja) * | 1983-03-18 | 1984-09-28 | Fuji Photo Film Co Ltd | 電子写真製版材料 |
| US4562132A (en) * | 1984-11-19 | 1985-12-31 | Xerox Corporation | Photoresponsive imaging members containing electron transport overcoatings |
| JP2718048B2 (ja) | 1988-02-15 | 1998-02-25 | 株式会社ブリヂストン | 電子写真感光体用電荷輸送剤及び電子写真感光体 |
| JPH01289966A (ja) * | 1988-05-17 | 1989-11-21 | Konica Corp | 感光体 |
| US4933246A (en) * | 1989-01-03 | 1990-06-12 | Xerox Corporation | Electrophotographic imaging member with a copolymer blocking layer |
| JP2714838B2 (ja) * | 1989-01-09 | 1998-02-16 | コニカ株式会社 | 電子写真感光体 |
| US4992349A (en) * | 1989-11-06 | 1991-02-12 | Eastman Kodak Company | Cyclic bis-dicarboximide charge transport compounds for electrophotography |
| US5110700A (en) * | 1990-12-28 | 1992-05-05 | Xerox Corporation | Electrophotographic imaging member |
| JPH0588396A (ja) * | 1991-09-27 | 1993-04-09 | Fuji Electric Co Ltd | 電子写真感光体 |
| JP2587748B2 (ja) | 1992-02-07 | 1997-03-05 | 株式会社巴川製紙所 | フルオレノン誘導体及びそれを用いた積層型電子写真感光体 |
| DE59407520D1 (de) | 1993-08-13 | 1999-02-04 | Ciba Geigy Ag | Perylenamidinimid-Farbstoffe, ein Verfahren zu deren Herstellung und deren Verwendung |
| JPH0770038A (ja) | 1993-08-31 | 1995-03-14 | Ricoh Co Ltd | フルオレン化合物およびそれを用いた電子写真感光体 |
| US5667097A (en) * | 1994-10-28 | 1997-09-16 | Joyce; Charles E. | Multiple pill dispensing unit |
| US5468583A (en) * | 1994-12-28 | 1995-11-21 | Eastman Kodak Company | Cyclic bis-dicarboximide electron transport compounds for electrophotography |
| TW311187B (enExample) * | 1994-12-28 | 1997-07-21 | Canon Kk | |
| JP2762962B2 (ja) | 1995-04-28 | 1998-06-11 | 日本電気株式会社 | 電子写真感光体 |
| JP3409540B2 (ja) | 1995-10-31 | 2003-05-26 | 富士ゼロックス株式会社 | 電子写真感光体およびそれを用いた画像形成装置 |
| US5795690A (en) * | 1995-11-21 | 1998-08-18 | Fuji Xerox Co., Ltd. | Electrophotographic photoreceptor, image forming apparatus and image forming process |
| JP3371662B2 (ja) | 1996-01-23 | 2003-01-27 | 富士ゼロックス株式会社 | 画像形成方法および画像形成装置 |
| US5641599A (en) * | 1996-01-11 | 1997-06-24 | Xerox Corporation | Electrophotographic imaging member with improved charge blocking layer |
| JP3384231B2 (ja) * | 1996-03-21 | 2003-03-10 | 富士ゼロックス株式会社 | 電子写真感光体及びそれを用いる画像形成装置 |
| ES2212769T3 (es) * | 1999-02-03 | 2004-08-01 | Basf Coatings Ag | Poliuretano y su utilizacion en el lacado acuoso de plasticos. |
| EP1361248B1 (en) * | 2001-01-15 | 2009-07-22 | Unitika Ltd. | Aqueous polyolefin resin dispersion |
| JP3699935B2 (ja) | 2001-01-15 | 2005-09-28 | ユニチカ株式会社 | ポリオレフィン樹脂水性分散体及びその製造方法 |
| JP2002341570A (ja) * | 2001-03-12 | 2002-11-27 | Kyocera Mita Corp | 電子写真感光体 |
| EP1241529A3 (en) * | 2001-03-12 | 2003-10-22 | Kyocera Mita Corporation | Electrophotosensitive material |
| JP2003029440A (ja) * | 2001-07-17 | 2003-01-29 | Konica Corp | 電子写真感光体、画像形成方法、画像形成装置及びプロセスカートリッジ |
| FR2828198B1 (fr) * | 2001-07-31 | 2007-02-23 | Atofina | Polypropylene isotactique obtenu par catalyse metallocene greffe |
| FR2828493B1 (fr) | 2001-08-07 | 2005-06-03 | Atofina | Composition a base de polypropylene et d'un copolymere ethylene/acrylate d'alkyle |
| JP3712062B2 (ja) * | 2002-02-04 | 2005-11-02 | 富士電機画像デバイス株式会社 | 電子写真用感光体およびこれを用いた電子写真装置 |
| JP3937873B2 (ja) * | 2002-03-01 | 2007-06-27 | キヤノン株式会社 | 電子写真感光体、プロセスカートリッジ及び電子写真装置 |
| JP4005392B2 (ja) | 2002-03-13 | 2007-11-07 | ユニチカ株式会社 | 水性分散体および積層フィルム |
| JP4378074B2 (ja) | 2002-08-30 | 2009-12-02 | キヤノン株式会社 | ナフタレンアミジンイミド化合物を含有する電子写真感光体、該電子写真感光体を有するプロセスカートリッジおよび電子写真装置 |
| JP4400366B2 (ja) * | 2004-08-06 | 2010-01-20 | 富士ゼロックス株式会社 | 電子写真感光体及びその製造方法、電子写真装置、並びにプロセスカートリッジ |
| JP4649321B2 (ja) * | 2005-11-30 | 2011-03-09 | キヤノン株式会社 | 電子写真感光体、プロセスカートリッジ及び電子写真装置 |
| US8617648B2 (en) * | 2006-02-01 | 2013-12-31 | Xerox Corporation | Imaging members and method of treating an imaging member |
| JP5064815B2 (ja) | 2007-01-26 | 2012-10-31 | キヤノン株式会社 | 新規なイミド化合物、電子写真感光体、プロセスカートリッジ及び電子写真装置 |
| JP5430353B2 (ja) * | 2009-11-02 | 2014-02-26 | キヤノン株式会社 | 電子写真感光体、プロセスカートリッジおよび電子写真装置 |
-
2009
- 2009-11-02 JP JP2009252076A patent/JP5430352B2/ja not_active Expired - Fee Related
- 2009-11-25 US US12/625,801 patent/US8632931B2/en not_active Expired - Fee Related
- 2009-11-26 EP EP09177199.8A patent/EP2317391B1/en not_active Not-in-force
- 2009-11-27 CN CN2009101784000A patent/CN102053511B/zh not_active Expired - Fee Related
- 2009-11-27 KR KR1020090115610A patent/KR101248267B1/ko not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5815776A (en) * | 1994-11-22 | 1998-09-29 | Fuji Xerox Co., Ltd. | Electrophotographic apparatus with photoreceptor having undercoat layer, containing an electronic transporting pigment and reactive organometallic compound |
| US5677097A (en) * | 1996-01-18 | 1997-10-14 | Fuji Xerox Co., Ltd. | Electrophotographic photoreceptor |
Also Published As
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|---|---|
| US8632931B2 (en) | 2014-01-21 |
| KR20110048437A (ko) | 2011-05-11 |
| EP2317391A1 (en) | 2011-05-04 |
| JP5430352B2 (ja) | 2014-02-26 |
| EP2317391B1 (en) | 2015-09-23 |
| CN102053511A (zh) | 2011-05-11 |
| KR101248267B1 (ko) | 2013-03-27 |
| US20110143273A1 (en) | 2011-06-16 |
| JP2011095665A (ja) | 2011-05-12 |
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Granted publication date: 20130501 |