JP3416401B2 - Electrophotographic photoreceptor, process cartridge and electrophotographic apparatus - Google Patents

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrophotographic photosensitive member, a process cartridge having the electrophotographic photosensitive member and an electrophotographic apparatus, and more specifically, an electrophotographic photosensitive member having a photosensitive layer containing a specific resin and a charge transfer agent. The present invention relates to a body, a process cartridge having the electrophotographic photosensitive member, and an electrophotographic apparatus.

[0002]

2. Description of the Related Art An electrophotographic method is disclosed in US Pat.
As disclosed in Japanese Patent Publication No. 91-91, a photoconductive material, which has a support whose electric resistance changes according to the amount of irradiation received during image exposure and which is coated with an insulating material in a dark place, is used. Is done. The basic characteristics required for an electrophotographic photosensitive member using this photoconductive material are (1) being able to be charged to an appropriate potential in a dark place, (2) being small in dissipation of the charge in a dark place, (3) Immediately dissipating the electric charge by light irradiation.

Conventionally, as an electrophotographic photoreceptor, an inorganic photoreceptor having a photosensitive layer containing an inorganic photoconductive compound such as selenium, zinc oxide or cadmium sulfide as a main component has been widely used. However, although these satisfy the above conditions (1) to (3), they are not always satisfactory in terms of thermal stability, moisture resistance, durability and productivity.

In order to overcome the drawbacks of inorganic photoconductors, electrophotographic photoconductors containing various organic photoconductive compounds as main components have been actively developed in recent years. For example, US Pat.
No. 8,378,851 discloses a photoreceptor having a charge-transporting layer containing triallylpyrazolin, which is disclosed in US Pat.
Japanese Patent Laid-Open No. 80 discloses a photoreceptor including a charge generation layer made of a derivative of a perylene pigment and a charge transport layer made of a condensation product of 3-propylene and formaldehyde.

Further, with respect to the organic photoconductive compound, the photosensitive wavelength region of the electrophotographic photosensitive member can be freely selected depending on the kind of the compound. For example, in the case of azo pigments, JP-A-61-272754, JP Kaisho 56-167759
The substance disclosed in the publication has high sensitivity in the visible region. Further, JP-A-57-19576 and JP-A-61-228.
It was of Gobutsu that shown in 453 JP is described as having a sensitivity to the infrared region.

Of these materials, those exhibiting sensitivity in the infrared region are used in laser beam printers (hereinafter abbreviated as LBP) and LED printers, which have made remarkable progress in recent years,
The demand frequency is increasing.

An electrophotographic photoreceptor using these organic photoconductive compounds is a function-separated photoreceptor in which a charge transport layer and a charge generation layer are laminated in order to satisfy both electrical and mechanical characteristics. Often used. On the other hand, as a matter of course, the electrophotographic photosensitive member is required to have sensitivity, electrical characteristics, and optical characteristics according to the electrophotographic process to be applied.

Particularly, in an electrophotographic photosensitive member that is repeatedly used, the surface of the electrophotographic photosensitive member is directly exposed to electrical or mechanical external force such as corona or direct charging, image exposure, toner development, transfer process, surface cleaning. Since they are added, durability against them is also required.

Specifically, electrical deterioration due to ozone and nitrogen oxides at the time of charging, mechanical deterioration such as abrasion and scratches on the surface due to discharge at the time of charging, rubbing of a cleaning member, and electrical deterioration Durability against static deterioration is required.

The electrical deterioration is particularly problematic in that the carrier stays in the light-irradiated portion and a potential difference occurs between the light-irradiated portion and the non-light-irradiated portion, which occurs as a photo memory.

[0011] Mechanical deterioration is inferior to mechanical deterioration in organic photoreceptors, which are often materially soft, unlike inorganic photoreceptors, and improvement in durability is particularly desired.

Various attempts have been made to satisfy the durability characteristics required for the above-mentioned photoreceptor.

[0013]

Polycarbonate resin having bisphenol A as a skeleton has been attracting attention as a resin which is often used for a surface layer and has good wear resistance and electric characteristics. However, it has the following problems.

(1) It has poor solubility and shows good solubility only in a part of halogenated aliphatic hydrocarbons such as dichloromethane and 1,2-dichloroethane, and since these solvents have low boiling points, When a photoconductor is manufactured using a coating liquid prepared from any of these solvents, the coated surface is likely to whiten.
It also takes time to manage the solid content of the coating liquid.

(2) For solvents other than halogenated aliphatic hydrocarbons, it is partially soluble in tetrahydrafuran, dioxane, cyclohexanone or a mixed solvent thereof, but the solution gels in a few days. As a result, the aging property is poor and it is not suitable for producing a photoreceptor.

(3) Even if the above (1) and (2) are improved, solvent cracks are easily generated in the polycarbonate resin having bisphenol A as a skeleton.

(4) In addition, in the conventional polycarbonate resin, the coating film formed of the resin has no lubricity,
If the cleaning settings are set so that the photoconductor is easily scratched and the amount of wear of the electrophotographic photoconductor is reduced, image defects may occur, or cleaning failure due to early deterioration of the cleaning blade or toner fusion may occur. It was

Regarding the solution stability mentioned in the above (1) and (2), a polycarbonate Z resin having a bulky cyclohexylene group is used as a structural unit of the polymer or is copolymerized with bisphenol Z, bisphenol C or the like. Has been solved by letting.

Solvent cracks can also be solved by using silicone-modified polycarbonate or ether-modified polycarbonate as disclosed in JP-A-6-51544 and JP-A-6-75415. is there. However, these modified polycarbonates have a structure that has flexibility against internal stress in the polymer in order to prevent solvent cracks as compared with conventional polycarbonate resins, and as a result, the mechanical strength of the polymer body is reduced. There was a drawback to do.

Further, in recent years, a direct charging system as disclosed in JP-A-57-17826 and JP-A-58-40566, in which a voltage is directly applied to a charging member to apply an electric charge to an electrophotographic photosensitive member. Is becoming mainstream.

This is a method in which a roller-shaped charging member made of conductive rubber or the like is directly brought into contact with an electrophotographic photosensitive member to apply an electric charge, and the amount of ozone generated is much smaller than that of a scorotron. Scorotron is wasted because about 80% of the current flowing in the charger is wasted because it flows in the shield, while direct electrification has the merit that it is very economical because there is no such waste.

However, the direct charging has a drawback that the charging stability is very poor because it is charged by the discharge according to Paschen's law. As a countermeasure against this, a so-called AC / DC charging method in which an AC voltage is superimposed on a DC voltage has been devised (Japanese Patent Laid-Open No. 63-149668).

By this charging method, the stability at the time of charging is improved, but the amount of discharge on the surface of the electrophotographic photosensitive member is greatly increased due to the superposition of AC, and the scraped amount of the electrophotographic photosensitive member is increased. A new defect that the number is increased has come to be demanded for not only mechanical strength but also electric strength.

The object of the present invention is to solve the problem of having a conventional polycarbonate resin as a surface layer, to have solvent crack resistance, high mechanical strength, and good electrical resistance characteristics by direct charging. The purpose of the present invention is to provide an electrophotographic photosensitive member that is easy to manufacture.

[0025]

That is, the present invention provides an electrophotographic photoreceptor having a photosensitive layer on a conductive support ,
The photosensitive layer has a charge generation layer and a charge transport layer,
In the electrophotographic photosensitive member in which the transport layer is the surface layer , the surface layer has the following formula (8).

[0026]

[Chemical 3] A polymer having a structural unit represented by the following formula (9),
(11), (13) and (14)

[0027]

[Chemical 4] A compound selected from the group consisting of:

The electrophotographic photoreceptor according to the present invention has particularly excellent solvent crack resistance and mechanical strength by selecting a combination of the above-mentioned resin and charge transfer agent as the resin and charge transfer agent forming the surface layer. It also has excellent electrophotographic characteristics in addition to the electric resistance characteristics in AC charging.

The present invention also provides a process cartridge and an electrophotographic apparatus having the above electrophotographic photosensitive member.

[0030]

BEST MODE FOR CARRYING OUT THE INVENTION The polyarylate resin used in the present invention is a single resin having a structural unit represented by the formula (8).
Even a polymer composed of
It may be a copolymer consisting of
Examples are shown in structural unit examples 2 to 9 in Table 1, but the present invention is not limited to these.

[0031]

[Table 1]

Polyarylate used in the present invention
The resin is obtained by interfacial polymerization which is carried out by stirring the bisphenol represented by the following formula (20) with a mixture of terephthalic acid chloride and isophthalic acid chloride in a solvent / water system under an alkaline condition in order to increase the solubility. be able to.

The ratio of terephthalic acid chloride to isophthalic acid chloride is determined in consideration of the solubility of the polymer, and there is no established theory. However, either chloride is 30 mol%
If the amount is below, the solubility of the synthesized polymer will be extremely lowered, so care must be taken.

Usually, it is preferable to synthesize them at a ratio of 1/1.

[0035]

[Chemical 5]

[0036] (X is, -CR ₃ R ₄ - (provided that R ₃ and R ₄ each independently represent a hydrogen atom, a trifluoromethyl group, an alkyl group having 1 to 6 carbon atoms or an aryl group having 6 to 12 carbon atoms, , 1-cycloalkylene group having 5 to 11 carbon atoms which may be substituted, α, ω having 2 to 10 carbon atoms
- an alkylene group, a single bond, -〇 -, - S -, - SO- or -SO ₂ - is. R _{1 and} R ₂ are each independently a hydrogen atom, a halogen atom, an optionally substituted alkyl group,
It is an aryl group or an alkylene group, and a and b are each independently an integer of 0 to 4. )

The polyarylate resin of the present invention is constructed in a different kind.
When used as a copolymer composed of units , a copolymer composed of structural unit example 1 and structural unit example 2 is particularly preferable.

In the electrophotographic photoreceptor of the present invention, the formula
Charges represented by (9), (11), (13), and (14)
You may use one type of transport material, or mix two or more types.
The charge transport material used when mixed
A body example is shown below.

[0039]

[Chemical 6]

[0040]

[Chemical 7]

[0041]

[Chemical 8]

[0042]

[Chemical 9]

The constitution of the electrophotographic photosensitive member used in the present invention will be described below.

The electrophotographic photosensitive member of the present invention is a laminated type in which the photosensitive layer is separated into a charge transport layer and a charge generating layer.

The conductive substrate to be used may be one having conductivity, and a metal such as aluminum or stainless steel,
Alternatively, metal, paper, plastic, or the like provided with a conductive layer may be used, and the shape may be a sheet shape, a cylindrical shape, or the like.

When the image input is laser light such as LBP, a conductive layer may be provided for the purpose of preventing interference fringes due to scattering or covering scratches on the substrate. This can be formed by dispersing a conductive powder such as carbon black or metal particles in a binder resin. The thickness of the conductive layer is 5
40 μm, preferably 10 to 30 μm is suitable.

An intermediate layer having an adhesive function is provided thereon. As the material of the intermediate layer, polyamide, polyvinyl alcohol, polyethylene oxide, ethyl cellulose,
Casein, polyurethane, polyether urethane, etc. may be mentioned. These are dissolved in a suitable solvent and applied. The thickness of the intermediate layer is 0.05 to 5 μm, preferably 0.3 to 1 μm.

A charge generation layer is formed on the intermediate layer.
The charge generating substance used in the present invention includes selenium-tellurium, pyrylium, thiapyrylium dye, phthalocyanine, anthanthrone, dibenzpyrenequinone, trisazo, cyanine, disazo, monoazo, indigo,
Examples include quinacridone and asymmetric quinocyanine pigments. For function-separated type, homogenizer with a binder resin and a solvent of 0.3 to 4 times the pre-Symbol charge generating substance of the charge generating layer, ultrasonic dispersion, a ball mill, a vibrating ball mill, sand mill, attritor, roll mill and the liquid It is well dispersed by a method such as a collision type high speed disperser, and the dispersion is applied and dried to be formed. The thickness of the charge generation layer is 5 μm
Below, 0.1 to 2 μm is preferable.

The charge transport layer is formed mainly by coating and drying a coating material obtained by dissolving the charge transport material and the binder resin in the present invention in a solvent.

These are combined with 0.5 to 2 times the amount of binder resin and coated and dried to form a charge transport layer.
The thickness of the charge transport layer is 5 to 40 μm, preferably 15 to
30 μm is suitable.

FIG. 1 shows a schematic structure of an electrophotographic apparatus having a process cartridge having the electrophotographic photosensitive member of the present invention.

In the figure, reference numeral 1 denotes a drum-shaped electrophotographic photosensitive member of the present invention, which is rotationally driven around a shaft 2 in a direction of an arrow at a predetermined peripheral speed. The photoconductor 1 rotates during the rotation process.
The peripheral surface of the primary charging means 3 is uniformly charged with a positive or negative predetermined potential, and then image exposure light 4 from an image exposure means (not shown) such as slit exposure or laser beam scanning exposure is received. In this way, electrostatic latent images are sequentially formed on the peripheral surface of the photoconductor 1.

The formed electrostatic latent image is then developed by the developing means 5.
The toner-developed image is developed by the toner, and the developed toner-developed image is taken out from a paper feeding unit (not shown) between the photoconductor 1 and the transfer means 6 in synchronization with the rotation of the photoconductor 1 and fed to the transfer material 7, The images are sequentially transferred by the transfer means 6.

The transfer material 7 which has received the image transfer is separated from the surface of the photoconductor and introduced into the image fixing means 8 to undergo the image fixing, so that it is printed out to the outside of the apparatus as a copy.

The surface of the photoconductor 1 after the image transfer is cleaned by the cleaning means 9 after removal of the transfer residual toner, and the pre-exposure light 10 from the pre-exposure means (not shown).
It is used for repeated image formation after being neutralized by. If the primary charging means 3 is a contact charging means using a charging roller or the like, pre-exposure is not always necessary.

In the present invention, among the constituent elements such as the electrophotographic photosensitive member 1, the primary charging means 3, the developing means 5 and the cleaning means 9, a plurality of components are integrally combined as a process cartridge, The process cartridge may be detachably attached to the main body of the electrophotographic apparatus such as a copying machine or a laser beam printer. For example, at least one of the primary charging unit 3, the developing unit 5, and the cleaning unit 9 is integrally supported together with the photoconductor 1 to form a cartridge, and the cartridge can be attached to and detached from the apparatus body by using a guide unit such as a rail 12 of the apparatus body. It can be the process cartridge 11.

Further, when the electrophotographic apparatus is a copying machine or a printer, the image exposure light 4 is reflected light or transmitted light from the original, or the original is read by a sensor and converted into a signal, which is performed in accordance with this signal. Laser beam scanning,
It is the light emitted by driving the LED array and driving the liquid crystal shutter array.

On the other hand, when used as a printer for a facsimile, the image exposure light 4 becomes exposure light for printing received data. FIG. 2 is a block diagram showing an example of this case.

The controller 14 controls the image reading section 13 and the printer 22. The entire controller 14 is controlled by the CPU 20. The read data from the image reading unit 13 is transmitted to the partner station through the transmission circuit 16. The data received from the partner station is sent to the printer 22 through the receiving circuit 15. Predetermined image data is stored in the image memory. The printer controller 21 controls the printer 22. 17 is a telephone.

The image received from the line 18 (image information from a remote terminal connected via the line) is demodulated by the receiving circuit 15, and then the image information is decoded by the CPU 20 and sequentially stored in the image memory 19. To be done. Then, when at least one page of image is stored in the memory 19, the image of that page is recorded. The CPU 20 reads out the image information of one page from the image memory 19, and the printer controller 21 reads out one page of the decoded page. Send image information. The printer controller 21 is
When the image information of one page is received from the CPU 20, the printer 22 is controlled to record the image information of the page. The CPU 20 is receiving the next page during recording by the printer 22.

In this way, the image is received and recorded.

The electrophotographic photoreceptor of the present invention can be used not only in electrophotographic copying machines but also in laser beam printers, C
RT printer, LED printer, liquid crystal printer,
It can be widely used in electrophotographic application fields such as laser plate making.

A description will be given below according to an embodiment.

[0064]

Example 1 An Al cylinder of 30φ254 mm was used as a support, and a coating material composed of the following materials was applied onto the support by a dipping method, and heat-cured at 140 ° C. for 30 minutes to give a thickness of 15 μm. The conductive layer of was formed.

Conductive pigment: SnO ₂ coated barium sulfate 10 parts Resistance adjusting pigment: titanium oxide 2 parts Binder resin: phenol resin 6 parts Leveling material: silicone oil 0.001 part Solvent: methanol, methoxypropanol 0.2 / 0.8 20 copies

Next, a solution prepared by dissolving 3 parts of N-methoxymethylated nylon and 3 parts of copolymerized nylon in a mixed solvent of 65 parts of methanol and 30 parts of n-butanol was applied onto the conductive layer by a dipping method to form 0.5 μm. Was formed.

Next, the diffraction angles 2θ ± 0.2 ° in the X-ray diffraction spectrum of CuKα are 9.0 °, 14.2 °, 2
TiOPc having strong peaks at 3.9 ° and 27.1 °
4 parts and polyvinyl butyral (trade name: S-REC BM
2, Sekisui Chemical Co., Ltd.) and 60 parts of cyclohexanone were dispersed in a sand mill using φ1 mm glass beads for 4 hours, and then 100 parts of ethyl acetate was added to prepare a charge generation layer dispersion liquid. Apply this by dipping method and
A 3 μm charge generation layer was formed.

Next, 10 parts of the charge transfer agent described in Condition 1 of Table 2 and 10 parts of the polymer described in Condition 1 of Table 3 were dissolved in a mixed solvent of 30 parts of monochlorobenzene and 70 parts of dichloromethane.

This polymer had a predetermined biphenol (0.01
1 mol of sodium hydroxide (0.8 g) and tetramethylammonium chloride (1 g) dissolved in 100 ml of water 1
Into a liter mixer, 1,2-dichloroethane (30 ml) was added to terephthalic acid chloride (0.005
mol) and a solution of isophthalic acid chloride (0.005 mol) were added while stirring and stirred at high speed for 10 minutes.
After being left for a period of time, a 1,2-dichloroethane solution was recovered, and a large amount of hexane was added thereto to recover it as a polymer. It should be noted that after recovery, it was used after being washed with water, dissolved in chloroform, and subjected to a purification step by dropping methanol.

This paint was applied by a dipping method and dried at 120 ° C. for 2 hours to form a 25 μm charge transport layer.

[0071]

[Table 2]

[0072]

[Table 3]

Next, the evaluation will be described.

The apparatus is Hewlett-Packard LBP
"Laserjet 4pIus" (Process speed 7
1 mm / sec) was modified and used. In the modification, the constant current control was used for the primary charging control and the constant voltage control was used. The produced electrophotographic photosensitive member was subjected to paper passing durability at 28 ° C. and 90% RH with this apparatus. The sequence is set to an intermittent mode in which the printing is stopped once for each sheet.

If the toner is used up, the toner is replenished and the toner is durable until a problem occurs in the image.

Further, using a Taber abrasion tester using an abrasive tape, abrasion was carried out for 15 minutes, and the weight reduction amount at that time was measured.

Further, 3000 l is used as a part of the electrophotographic photosensitive member.
The light potential was measured after illuminating the light of a white fluorescent lamp for 10 minutes with ux and left for 10 minutes, and the amount of decrease in the light potential before the light was applied was measured to obtain a photomemory value.

[0078] Further solvent crack resistance was observed whether the left solvent crack by microscopic observation 48 hours to adhere the finger fat to the surface.

The results are shown in Table 4.

The molar ratio of terephthalic acid chloride and isophthalic acid chloride was 1: 1.

[0081] [Example 2-5] used as conditions 2 to 5 in Table 2 in the charge transport agent of the charge transport layer, except that used was a condition 2-5 in Table 3 in the binder as in Example 1 Similarly, an electrophotographic photosensitive member was prepared and evaluated.
The results are shown in Table 4.

[0082]

[Table 4]

[Comparative Examples 1 to 4] As the charge transporting agent of the charge transporting layer, Comparative Examples 1 and 2 are the following formula structures, Comparative Examples 3 and 4 are the tritolylamine materials represented by the formula (21), and the binder is used. An electrophotographic photosensitive member was prepared and evaluated in the same manner as in Example 1 except that the conditions 1 to 4 in Table 5 were used. The results are shown in Table 6.

[0084]

[Chemical 10]

[0085]

[Table 5]

[0086]

[Table 6]

Example 6 An Al cylinder of 30φ254 mm was used as a support, and a coating material composed of the following materials was applied onto the support by a dipping method and heat-cured at 140 ° C. for 30 minutes to obtain a conductive layer of 15 μm. Was formed.

Conductive pigment: SnO ₂ coated barium sulfate 10 parts Resistance adjusting pigment: titanium oxide 2 parts Binder resin: phenol resin 6 parts Leveling material: silicone oil 0.001 part Solvent: methanol, methoxypropanol 0.2 / 0.8 20 copies

Next, on this, 3 parts of N-methoxymethylated nylon and 3 parts of copolymerized nylon were mixed with 65 parts of methanol and n.
A solution of 30 parts of butanol dissolved in a mixed solvent was applied by a dipping method to form an intermediate layer of 0.5 μm.

Next, the diffraction angles 2θ ± 0.2 ° in the X-ray diffraction spectrum of CuKα are 9.0 °, 14.2 °, 2
TiOPc having strong peaks at 3.9 ° and 27.1 °
4 parts and polyvinyl butyral (trade name: S-REC BM
2, Sekisui Chemical Co., Ltd.) and 60 parts of cyclohexanone were dispersed for 4 hours in a sand mill using φ1 mm glass beads, and then 100 parts of ethyl acetate was added to prepare a dispersion liquid for a charge generation layer. Apply this by dipping method and
A 3 μm charge generation layer was formed.

Next, 8 parts of the charge transfer agent described in Condition 1 of Table 7 and 12 parts of the polymer described in Condition 1 of Table 8 were dissolved in a mixed solvent of 30 parts of monochlorobenzene and 70 parts of dichloromethane.

This coating material was applied by a dipping method and dried at 120 ° C. for 2 hours to form a 25 μm charge transport layer.

[0093]

[Table 7]

[0094]

[Table 8]

The mixing ratio of terephthalic acid chloride and isophthalic acid chloride was 1: 1 in terms of molar ratio.

The obtained electrophotographic photosensitive member was tested in the same manner as in Example 1, and the results are shown in Table 9. Example 7-11] electron as well as the charge transport layer of the charge transport material used as the condition 2-6 in Table 7, Example 6, except that used was a condition 2-6 in Table 8 Binder A photographic photoreceptor was prepared and evaluated.
The results are shown in Table 9.

[0097]

[Table 9]

[0098] Creating a Comparative Example 5-10] The charge transport layer a charge transport agent and Comparative Example No. structural unit 1, except that used was the 4 In the same manner as in Example 1 electrophotographic photosensitive member of the table 10 to the binder of And evaluated. The results are shown in Table 11.

[0099]

[Chemical 11]

[0100]

[Table 10]

[0101]

[Table 11]

[0102]

The electrophotographic photoreceptor of the present invention has excellent solvent crack resistance without impairing the mechanical strength, has high mechanical strength, and has good electric resistance characteristics against discharge by direct charging. It has become possible to provide an electrophotographic photosensitive member suitable for direct charging, which is easy to manufacture, a process cartridge having the electrophotographic photosensitive member, and an electrophotographic apparatus.

[Brief description of drawings]

FIG. 1 is a diagram showing an example of a schematic configuration of an electrophotographic apparatus having a process cartridge having an electrophotographic photosensitive member of the present invention.

FIG. 2 is a diagram showing an example of a block diagram of a facsimile having the electrophotographic photosensitive member of the present invention.

[Explanation of symbols]

1 Electrophotographic photoreceptor of the present invention 2 axes 3 Primary charging means 4 Image exposure light 5 Developing means 6 Transfer means 7 Transfer material 8 Image fixing means 9 Cleaning means 10 Pre-exposure light 11 Process cartridge 12 rails 13 Image reading section 14 Controller 15 Receiver circuit 16 Transmitter circuit 17 telephone 18 lines 19 Image memory 20 CPU 21 Printer controller 22 Printer

─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Yama ▲ saki ▼ To 3-30-2 Shimomaruko, Ota-ku, Tokyo Canon Inc. (72) Inventor Wataru Kitamura 3-30-2 Shimomaruko, Ota-ku, Tokyo Canon Inc. (56) Reference JP 62-135840 (JP, A) JP 61-53647 (JP, A) JP 8-95263 (JP, A) JP 7-295340 (JP, A) JP 7-225485 (JP, A) JP 7-92705 (JP, A) JP 6-273949 (JP, A) JP 6-27703 (JP, A) Kaihei 6-27695 (JP, A) JP 5-307274 (JP, A) JP 5-72751 (JP, A) JP 3-63653 (JP, A) JP 3-33860 ( JP, A) JP-A-3-6567 (JP, A) JP-A-2-96175 (JP, A) (58) Survey The field (Int.Cl. ^7, DB name) G03G 5/00

Claims (3)

(57) [Claims] 1. An electronic copy having a photosensitive layer on a conductive support.
A true photoconductor, in which the photosensitive layer is a charge generation layer and a charge transport layer.
In an electrophotographic photoreceptor having a transport layer and the charge transport layer being a surface layer , the surface layer is represented by the following formula (8) : A polymer having a structural unit represented by the following formula (9),
(11), (13) and (14) An electrophotographic photoreceptor containing a compound selected from the group consisting of: 2. The electrophotographic photosensitive member according to claim 1, and at least one means selected from the group consisting of a charging means, a developing means and a cleaning means are integrally supported and can be attached to and detached from the main body of the electrophotographic apparatus. There is a process cartridge. 3. An electrophotographic apparatus comprising the electrophotographic photosensitive member according to claim 1, a charging unit, an image exposure unit, a developing unit and a transfer unit.