JP2007161619A5 - - Google Patents

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Publication number
JP2007161619A5
JP2007161619A5 JP2005357650A JP2005357650A JP2007161619A5 JP 2007161619 A5 JP2007161619 A5 JP 2007161619A5 JP 2005357650 A JP2005357650 A JP 2005357650A JP 2005357650 A JP2005357650 A JP 2005357650A JP 2007161619 A5 JP2007161619 A5 JP 2007161619A5
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JP
Japan
Prior art keywords
parts
film thickness
structure represented
charge generation
generation layer
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Pending
Application number
JP2005357650A
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Japanese (ja)
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JP2007161619A (en
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Priority to JP2005357650A priority Critical patent/JP2007161619A/en
Priority claimed from JP2005357650A external-priority patent/JP2007161619A/en
Publication of JP2007161619A publication Critical patent/JP2007161619A/en
Publication of JP2007161619A5 publication Critical patent/JP2007161619A5/ja
Pending legal-status Critical Current

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Description

この分散液に、陽極酸化処理したアルミニウムシリンダーを浸漬塗布し、乾燥後の膜厚が0.3μm(着量0.3g/m2)となるように電荷発生層を作製した。
次に、電荷輸送物質として実施例3で製造した化合物60部と、バインダ樹脂として下記式(a)で表わされる構造を繰り返し単位として持つポリカーボネート(PC1;粘度平均分子量約30000)100部と、下記式(b)で表わされる構造を有する酸化防止剤8部と、レベリング剤としてシリコーンオイル(商品名:KF96,信越化学工業(株))0.05部とを、THF/トルエン(重量比8/2)混合溶媒640部に溶解させた液を、上述の電荷発生層上に、乾燥後の膜厚が18μmとなるように浸漬塗布し、積層型感光層を有する感光体ドラムA(感光体)を得た。
To this dispersion, the aluminum cylinder was anodized dip coating, the film thickness after drying to prepare a charge generation layer such that 0.3 [mu] m (Chakuryou 0.3g / m 2).
Next, 60 parts of the compound produced in Example 3 as a charge transport material, 100 parts of a polycarbonate (PC1; viscosity average molecular weight of about 30000) having a structure represented by the following formula (a) as a binder unit as a binder resin, 8 parts of an antioxidant having a structure represented by the formula (b), 0.05 part of silicone oil (trade name: KF96, Shin-Etsu Chemical Co., Ltd.) as a leveling agent, THF / toluene (weight ratio 8 / 2) Photosensitive drum A (photosensitive member) having a laminated type photosensitive layer by dip-coating the liquid dissolved in 640 parts of the mixed solvent on the above-described charge generation layer so that the film thickness after drying becomes 18 μm. Got.

JP2005357650A 2005-12-12 2005-12-12 Method for production of organic compound, electronic material obtained by the same and electronic device, electrophotographic photoreceptor, and image forming device using the same Pending JP2007161619A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2005357650A JP2007161619A (en) 2005-12-12 2005-12-12 Method for production of organic compound, electronic material obtained by the same and electronic device, electrophotographic photoreceptor, and image forming device using the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2005357650A JP2007161619A (en) 2005-12-12 2005-12-12 Method for production of organic compound, electronic material obtained by the same and electronic device, electrophotographic photoreceptor, and image forming device using the same

Publications (2)

Publication Number Publication Date
JP2007161619A JP2007161619A (en) 2007-06-28
JP2007161619A5 true JP2007161619A5 (en) 2008-09-25

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Family Applications (1)

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JP2005357650A Pending JP2007161619A (en) 2005-12-12 2005-12-12 Method for production of organic compound, electronic material obtained by the same and electronic device, electrophotographic photoreceptor, and image forming device using the same

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JP (1) JP2007161619A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015032847A1 (en) 2013-09-09 2015-03-12 Basf Se Polyarylene ether sulfone-polymers for membrane applications

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3162471B2 (en) * 1991-10-23 2001-04-25 帝人株式会社 Process for producing monoalkenylbenzene and its derivatives
JP4138067B2 (en) * 1998-02-17 2008-08-20 昭和化工株式会社 Method for producing methine derivative
DE19942394C1 (en) * 1999-09-06 2001-02-01 Bayer Ag Increasing the yield of nitrodiphenylamines in base/palladium-catalysed nitrohalobenzene/aromatic amine reactions by using a base which has been milled and optionally also dried
DE10005601A1 (en) * 2000-02-09 2001-08-16 Bayer Ag Process for the preparation of aminodiphenylamines

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