Electrophotographic photoreceptor and image forming apparatus including the same

An electrophotographic and photoreceptor technology, applied in optics, electrographics, instruments, etc., can solve the problems of poor production efficiency, easy deterioration and wear of the surface of the photosensitive layer, and achieve excellent wear resistance, excellent mechanical strength, high The effect of charge mobility

Active Publication Date: 2006-03-15
SHARP KK
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  • Abstract
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AI Technical Summary

Problems solved by technology

The problem that the practical organic photoreceptor has when it is repeatedly used is that it is easy to cause property changes such as a decrease in charge potential and an increase in residual potential due to film reduction of the photosensitive layer, electrical changes, and chemical changes.
Polyarylate-based resins have a similar structure to polycarbonate resins, but differ in properties from photoreceptors using these resins
It is known that a photoreceptor using a polyarylate system is excellent in mechanical strength, but when a polyarylate-based resin is used as a binder resin for a charge transport layer, it has the following disadvantages: Depending on the structure of the charge transport substance used , it is easy to cause property changes such as a decrease in the potential retention rate and an increase in the residual potential
[0041] (1) Poor solubility, only showing good solubility in some halogen organic solvents such as dichloromethane and 1,2-dichloroethane
Due to the low boiling point of these halogen-based organic solvents, if a coating solution prepared from these solvents is used to manufacture a photoreceptor, the evaporation rate of the solvent is too fast, and the coating film is prone to white turbidity due to the heat of vaporization.
In addition, halogen-based organic solvents such as dichloromethane and 1,2-dichloroethane are highly toxic and have a large impact on operators and the global environment due to the destruction of the ozone layer, and the management of the manufacturing process becomes complicated.
[0042] (2) In addition to the aforementioned halogen organic solvents, although they are partially soluble in tetrahydrofuran, dioxane, cyclohexanone or their mixed solvents, the coating liquid prepared with these solvents will condense within a few days after preparation. Gelling, etc., poor storage stability
In particular, when a photoreceptor is produced by dip coating, the coating liquid in the coating tank will gel, which hinders the production of the photoreceptor.
[0043] (3) Due to the strong intermolecular attraction of the resin itself, the formed coating film has poor adhesion and is prone to cracks at the interface with other layers
Therefore, tailing (tailing) of the coating film occurs to reduce productivity
In addition, when used as a photoreceptor, the toner adheres to the convex part and remains without being removed, which easily causes image defects due to so-called poor cleaning.
[0045] (5) Due to the lack of mechanical strength of the resin itself, the photosensitive layer using bisphenol A polycarbonate resin is prone to scratches on its surface due to the friction of charging rollers, magnetic brushes or cleaning shovels, and gradually wears away.
However, even if the high charge mobility enamine compound used in the photoreceptor described in the aforementioned JP-A-2-51162, JP-A-6-43674 or JP-A-10-69107 is used, in a low temperature environment Sufficient photoresponsiveness cannot be obtained
In addition, although the photoreceptor described in Japanese Unexamined Publication No. 7-134430 has a high charge transport ability by containing polysilane, there is a problem that the photoreceptor using polysilane has weak resistance to exposure, and the photoreceptor using polysilane has a weak resistance to exposure. In the light, the various properties of the photoreceptor are reduced
[0057] In addition, although the aforementioned corona discharge and gap discharge are used in the charging of the photoreceptor, there is a problem that the organic photoreceptor is decomposed and deteriorated by active gases such as ozone and NOx generated by these discharges. , so that the surface of the photosensitive layer is easy to deteriorate, and after repeated use, the electrical characteristics such as chargeability, sensitivity and responsiveness will be reduced, and the image quality will be deteriorated
[0060] The technique described in the aforementioned Japanese Patent Laid-Open No. 10-10761 cannot prevent the generation of defects by itself, so it cannot avoid the dielectric breakdown of the photosensitive layer.
In addition, since the charge transport layer is formed in this technology, the process of applying the coating liquid and the drying process must be repeated, and the production efficiency is poor.
[0061] In addition, the sensitivity and responsiveness of the photoreceptor described in JP-A-2001-56595 are not sufficient, and image defects such as background contamination and lowered image density occur when electrophotography is performed at high speed.
[0062] In addition, in order to form the charge-transporting layer of the photoreceptor in the technique described in JP-A-2001-166502, it is necessary to polymerize the hole-transporting compound by radiation or the like, so it is difficult to manufacture it with existing manufacturing equipment.

Method used

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  • Electrophotographic photoreceptor and image forming apparatus including the same
  • Electrophotographic photoreceptor and image forming apparatus including the same
  • Electrophotographic photoreceptor and image forming apparatus including the same

Examples

Experimental program
Comparison scheme
Effect test

preparation example 1

[0393] (Preparation Example 1) Preparation of Exemplary Compound No.1

[0394] (Preparation example 1-1) the preparation of enamine intermediate

[0395] In 100ml of toluene, add 23.3g (1.0 equivalent) of the N-(p-tolyl)-α-naphthylamine shown in the following structural formula (9) and 20.6g (1.05 equivalent) of the diphenyl group shown in the following structural formula (10) Acetaldehyde and 0.23g (0.01 equivalent) DL-10-camphorsulfonic acid were heated to make the by-product water and toluene azeotropic, discharged from the system, and the reaction was carried out for 6 hours. After the reaction was completed, the reaction solution was concentrated to about 1 / 10, and slowly added dropwise to 100 ml of hexane that was vigorously stirred to form crystals. The resulting crystals were filtered off and washed with cold ethanol to obtain 36.2 g of a pale yellow toner powder.

[0396]

[0397]

[0398] The obtained compound was analyzed by liquid chromatography-mass spectr...

preparation example 1-2

[0401] (Preparation example 1-2) the preparation of enamine-aldehyde intermediate

[0402] In 100 ml of anhydrous N,N-dimethylformamide (DMF), slowly add 9.2 g (1.2 equivalents) of phosphorus oxychloride under ice cooling, and stir for about 30 minutes to prepare the Wells-Meyer reagent. Under ice cooling, 20.6 g (1.0 equivalent) of the enamine intermediate represented by the aforementioned structural formula (11) prepared in Preparation Example 1-1 was slowly added to the solution. Then, it was heated slowly to raise the reaction temperature to 80° C. and kept at 80° C. with heating and stirring for 3 hours. After the reaction, the reaction solution was left to cool, and slowly added to 800 ml of cooled 4N aqueous sodium hydroxide solution to form a precipitate. The formed precipitate was filtered off, washed sufficiently with water, and then recrystallized from a mixed solvent of ethanol and ethyl acetate to obtain 20.4 g of a yellow toner powder.

[0403] The obtained com...

preparation example 3

[0419] (Preparation Example 3) Preparation of Exemplary Compound No.46

[0420] 2.0g (1.0 equivalents) of the enamine-aldehyde intermediate shown in the aforementioned structural formula (12) obtained in Preparation 1-2 and 1.53g (1.2 equivalents) of the Wittig reagent shown in the following structural formula (14) were dissolved in 15ml After slowly adding 0.71 g (1.25 equivalents) of potassium tert-butoxide to the solution in anhydrous DMF at room temperature, the solution was heated to 50° C. and stirred for 5 hours while maintaining and heating at 50° C. After the reaction mixture was allowed to cool, it was poured into excess methanol. The precipitate was collected and dissolved in toluene to prepare a toluene solution. The toluene solution was transferred to a separatory funnel, washed with water, and the organic layer was taken out, and the taken organic layer was dried over magnesium sulfate. After drying, the organic layer from which the solid matter was removed was...

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PUM

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Abstract

An electrophotographic photoreceptor of high durability capable of providing stable excellent electrical characteristics over a prolonged period of time, which electrophotographic photoreceptor excels in mechanical strength. Photosensitive layer (14) of electrophotographic photoreceptor (1) comprises a polyarylate resin having structural units, for example, those of aforementioned formula (1-3) and an enamine compound represented by, for example, aforementioned formula (2-1). By virtue of these, electrophotographic photoreceptor (1) of excellent mechanical strength and favorable electrical characteristics can be realized.

Description

technical field [0001] The present invention relates to an electrophotographic photoreceptor, a process cartridge having the electrophotographic photoreceptor, and an electrophotographic device, and more specifically, to an electrophotographic photoreceptor having a photosensitive layer containing a specific resin and a specific charge transporting substance , A process cartridge having an electrophotographic photoreceptor, and an electrophotographic device. [0002] The present invention also relates to an electrophotographic photoreceptor used in electrophotographic image forming devices such as copiers, printers, and facsimile devices, and an image forming device having the electrophotographic photoreceptor. An electrophotographic photoreceptor of a photosensitive layer of a specific charge-transporting substance and an image forming apparatus having the electrophotographic photoreceptor. [0003] The present invention relates to an image forming method and an image formin...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G03G5/06G03G5/05G03G5/14
Inventor 森田龙广金泽朋子近藤晃弘竹沢洋一小幡孝嗣三村晋也杉村博
Owner SHARP KK
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