JPH08234456A - Electrophotographic photoreceptor and its production - Google Patents

Abstract

PURPOSE: To solve problems on compatibility, the viscosity of a coating soln., the interlayer peeling and cracking of a photoreceptor and to suppress the rise of residual potential by using a blend of two kinds of specified resins as a resin binder contained in a photosensitive layer. CONSTITUTION: In the electrophotographic photoreceptor consisting of an electrically conductive substrate 1 and a photosensitive layer 4 formed on the substrate 1 and contg. at least an electric charge generating material and an electric charge transferring material, a resin binder contained in the photosensitive layer 4 is made of a blend of a 1 st resin having 130-200 deg.C glass transition temp. with a 2nd resin having 0-80 deg.C glass transition temp. The 1st resin is, e.g. polycarbonate resin or polyarylate resin. The 2nd resin is, e.g. polyester resin consisting of arom. dicarboxylic acid and glycol and typified by polyethylene terephthalate.

Description

Detailed Description of the Invention

[0001]

FIELD OF THE INVENTION The present invention relates to an electrophotographic photoreceptor. Specifically, even when it is repeatedly used by using a specific binder resin, it exhibits stable electrical characteristics in which a decrease in charging potential and an increase in residual potential are suppressed, and peeling and cracking of a photosensitive layer in the manufacturing process of a photoreceptor. The present invention relates to an electrophotographic photosensitive member that suppresses the occurrence of cracks and the like.

[0002]

2. Description of the Related Art In recent years, electrophotographic technology has been widely used not only for copying machines but also for various printers and facsimiles because of its immediacy and high image quality. In particular, the photoconductor has conventionally been used as an inorganic photoconductor such as selenium, cadmium sulfide, arsenic-selenium alloy, zinc oxide, or amorphous silicon as a photoconductive material, but recently, it is non-polluting. 400 to 80 because of easy film formation and easy manufacturing
A large number of photoconductors using organic photoconductors, which have a sensitivity higher than that of inorganic systems in a wide range of 0 nm, have been developed and used.

In particular, it is a dispersion type photoconductor in which a low molecular weight organic photoconductive compound is dispersed in a binder resin as an organic photoconductor, and a function separation type laminated photoconductor in which a charge generation layer and a charge transport layer are independently laminated. In the body, a highly sensitive photoreceptor can be obtained by combining an efficient charge generating substance and a charge transporting substance in the charge generating layer and the charge transporting layer. Further, it is mainly studied because the materials can be selected in a wide range and a highly safe photoreceptor can be obtained, and the coating property is excellent and the cost is relatively advantageous.

However, the function-separated layered photoconductors currently in practical use are inferior in durability to the conventional inorganic photoconductors. In particular, sensitivity deterioration due to deterioration in electrical characteristics such as decrease in charging potential and increase in residual potential during repeated use, sensitivity deterioration due to abrasion or scratch on the surface of the photoconductor, or image defects are likely to occur. These are impurities, organic photoconductive compounds in the photosensitive layer, deterioration of the binder resin and formation of structural carrier traps, toner, developer, paper, during charging, exposure, development, transfer and cleaning processes.
At present, there is a limit to the printing durability in practical use because it has a drawback that the surface of the photosensitive member is easily worn or damaged by contact with a cleaning member due to chemical or mechanical load.
In addition, due to the problem that image quality defects are caused by foreign matter such as toner filming, low resistance substances such as ozone and nitrogen oxides generated by corona discharge, and paper dust generated by copy paper are deposited and accumulated on the photoreceptor surface. There is a problem such as image deletion in a high temperature and high humidity environment, which significantly limits the life of the photoconductor.

Generally, in a negative charging type laminated photoreceptor, the surface layer of the photoreceptor is a charge transport layer. The charge transport layer forms a solid solution in which the charge transport substance is dissolved in the binder resin at a concentration of 30 to 60%, and has no inherent mechanical strength of the binder resin, resulting in a very brittle film that easily wears and is easily scratched. . At this time, the compatibility between the binder resin and the charge transport material is also an extremely important factor, and if the compatibility is poor, the charge transport material may be crystallized and the electrical characteristics and the image quality characteristics may be significantly adversely affected. well known.

With respect to such problems, studies on binder resins for various surface layers of photoreceptors have been reported. JP-A-6-59471 discloses blending with a specific polycarbonate, and JP-A-5-34951 discloses polycarbonate. A blend resin of polyetherimide, polyurethane, and aromatic polyester resin is disclosed. In these cases, the solubility of the resin to be used is of course important, and the compatibility of the blended resin is important, and there is a problem in that when a combination having a poor compatibility is used, unevenness of images and black spots may occur when a photoconductor is used.

Further, Japanese Patent Application Laid-Open No. 1-206348 discloses a method of using a high molecular weight binder resin, but the viscosity of the coating solution for the charge transport layer becomes high, and defoaming of bubbles caused by stirring or circulation operation occurs. It is difficult and there is a problem in coatability.

Further, a method in which the photosensitive layer is formed by dip coating on a conductive support or an underlayer is generally used, but internal stress is accumulated in the steps of drying and solvent evaporation. May cause delamination, cracks and cracks. The degree of internal stress accumulation in these steps depends on the degree of solvent diffusion between the layers and the stress relaxation of the layers. Here, it is known that the stress relaxation has a close correlation with the drying temperature, the drying time and the properties peculiar to the substance, and the glass transition temperature is an important factor. Generally, as the glass transition temperature of the photoconductor becomes lower, relaxation of the substance is more likely to occur during the drying process of the photoconductor, and the accumulation of internal stress is less likely to occur. JP-A-6-5
No. 9469 contains 2 parts in the binder resin in order to reduce internal stress and prevent delamination, cracks and cracks of the photoreceptor.
Although a photoreceptor having a lower glass transition temperature by containing one or more kinds of charge transport substances is disclosed, the glass transition temperature of the binder resin has not been examined.

As described above, in order to solve the problems of the durability and the manufacturing process of the photoreceptor using the organic material, the charge transport material and the binder resin or the binder resin used in the photosensitive layer or the charge transport layer are used. It is necessary to simultaneously solve the problems of mutual compatibility, viscosity of the coating solution, delamination of the photoconductor, and generation of cracks and cracks, which is often insufficient at present.

[0010]

DISCLOSURE OF THE INVENTION The present invention is directed to the compatibility of the charge transport material used in the above-mentioned photosensitive layer and charge transport layer with the binder resin and the binder resin, the viscosity of the coating solution,
A highly durable electrophotographic photoconductor that simultaneously solves the problems of delamination, cracking, and cracking of the photoconductor, and shows stable electrical characteristics that prevent the charging potential from decreasing and the residual potential from increasing even after repeated use. The purpose is to provide.

[0011]

Means for Solving the Problems The present inventors have made a detailed study on the binder resin used in the photosensitive layer. As a result, when a resin obtained by blending two or more kinds of resins having different glass transition temperatures is used, the electrical conductivity of the photoconductor is improved. It has been found that the characteristics are stable and the peeling and cracking of the photosensitive layer can be suppressed.

After further diligent examination, 130 ° C. or more 20
A first binder resin having a glass transition temperature of 0 ° C. or lower and a second binder resin having a glass transition temperature of 0 ° C. to 80 ° C.
The present invention has been completed by finding that a photoreceptor using a resin blended with the above binder resin shows repeated charging characteristics excellent in stability and has practically sufficient mechanical performance.

That is, the electrophotographic photosensitive member according to claim 1 of the present invention is an electrophotographic photosensitive member comprising a conductive support and a photosensitive layer which is formed thereon and which contains at least a charge generating substance and a charge transporting substance. In the body, the binder resin contained in the photosensitive layer is a blend of a first resin having a glass transition temperature of 130 ° C. to 200 ° C. and a second resin having a glass transition temperature of 0 ° C. to 80 ° C. It is a resin characterized by the above.

According to a second aspect of the present invention, the electrophotographic photosensitive member has a charge generating layer containing at least a charge generating substance and a charge transporting layer containing a charge transporting substance on a conductive support. In the laminated electrophotographic photosensitive member which is configured by independently separating the functions, the binder resin of the charge transport layer comprises a first resin having a glass transition temperature of 130 ° C. or higher and 200 ° C. or lower, and a binder resin of 0 ° C. or higher and 80 ° C. or lower. The resin is a blend of a second resin having a glass transition temperature.

Further, in the electrophotographic photosensitive member according to claim 3 of the present invention, the first resin constituting the binder resin is
It is characterized by being a polycarbonate resin or a polyarylate resin having a viscosity average molecular weight of 30,000 to 50,000.

In the electrophotographic photosensitive member of claim 4 according to the present invention, the second resin constituting the binder resin is
A polyester resin having a viscosity average molecular weight of 20,000 to 40,000 or a viscosity average molecular weight of 50,000 to 80,
000 acrylic resin.

According to a fifth aspect of the present invention, there is provided a method for manufacturing an electrophotographic photosensitive member, in which a photosensitive layer containing at least a charge generating substance and a charge transporting substance is dipped on a drum-shaped conductive support. In the method for producing an electrophotographic photosensitive member,
The binder resin concentration in the photosensitive layer coating solution is 7% by weight.
To 13% by weight.

According to a sixth aspect of the present invention, in the method for producing an electrophotographic photosensitive member, a charge-generating layer containing at least a charge-generating substance and a charge-transporting substance are contained on a drum-shaped conductive support. In a method for manufacturing a laminated electrophotographic photosensitive member, which is configured by independently immersing a charge transport layer,
The binder resin concentration in the charge transport layer coating liquid is 7% by weight.
To 13% by weight.

The present invention will be described in detail below.

The constitution of the electrophotographic photosensitive member of the present invention is as follows:
As shown in FIG. 1, a photosensitive layer having a charge-generating layer and a charge-transporting layer, which is a function-separated type photoreceptor, and a charge-transporting layer having a charge-generating substance dispersed therein, as shown in FIG. Or Figure 2
As described above, an undercoat layer may be provided as an intermediate layer between the conductive support and the photosensitive layer.

The electrophotographic photoreceptor of the present invention is provided with a photosensitive layer on a conductive support, and the conductive support is made of a metal material such as aluminum, stainless steel, copper or nickel.
An insulating support such as a polyester film having a conductive layer of aluminum, copper, palladium, tin oxide, indium oxide or the like on its surface, a phenol resin pipe, a paper tube, or the like is used.

A general intermediate layer may be provided between the conductive support and the photosensitive layer. For the middle layer,
Polyamide, polyurethane, cellulose, nitrocellulose, polyvinyl alcohol, polyvinylpyrrolidone,
Polyacrylamide, aluminum anodic oxide coating, gelatin, starch, casein, N-methoxymethylated nylon and the like are used. Further, particles of titanium oxide, tin oxide or aluminum oxide may be dispersed in these.

Se and its alloys, arsenic-selenium, cadmium sulfide, zinc oxide, amorphous silicon, other inorganic photoconductors, phthalocyanines, azo compounds, quinacridones, polycyclic quinones, perylene, etc., as charge generating materials in the charge generating layer. Organic dyes such as organic pigments, thiapyrylium salts, and squarylium salts are used. In the charge generation layer, an electron accepting material as a chemical sensitizer, for example, tetracyanoethylene, cyano compounds such as 7,7,8,8-tetracyanoquinodimethane, anthraquinone, quinones such as p-benzoquinone, Nitro compounds such as 2,4,7-trinitrofluorenone and 2,4,5,7-tetranitrofluorenone, or dyes such as xanthene dyes, thiazine dyes and triphenylmethane dyes as optical sensitizers. You may add.

As the method of forming the charge generating layer, a vapor deposition method such as vacuum vapor deposition, sputtering or CVD, melting of the charge generating material, or ball mill, sand grinder,
Grind and disperse with a paint shaker, ultrasonic disperser, etc., add binder resin if necessary, baker applicator, bar coater, casting, spin coat etc. for sheet, spray method for drum, vertical ring And the dip coating method.

As the binder resin, polyarylate,
Polyvinyl butyral, polycarbonate, polyester, polystyrene, polyvinyl chloride, phenoxy, epoxy, silicone resin, acrylic resin and the like are used.

Examples of the solvent include ketones such as acetone, methyl ethyl ketone and cyclohexanone, esters such as ethyl acetate and butyl acetate, ethers such as tetrahydrofuran and dioxane, aromatic hydrocarbons such as benzene, toluene and xylene, and N, N. -Aprotic polar solvents such as dimethylformamide and dimethylsulfoxide can be used.

The film thickness is 0.05 to 5 μm, preferably 0.08 to 1 μm.

As the charge transport material in the charge transport layer, a polymer compound such as polyvinylcarbazole or polysilane,
Low molecular weight compounds such as hydrazone compounds, pyrazoline compounds, oxadiazole compounds, stilbene compounds, triphenylmethane compounds, triphenylamine compounds and enamine compounds are used.

As the method for forming the charge transport layer, the charge transport material is dissolved in a solvent, the binder resin of the present invention is added, and in the case of a sheet, a baker applicator, a bar coater,
In the case of a drum such as casting or spin coating, it is prepared by a spray method, a vertical ring method, or a dip coating method.

As a binder resin for the charge transport layer, 13
A resin obtained by blending a first binder resin having a glass transition temperature of 0 ° C. to 200 ° C. and a second binder resin having a glass transition temperature of 0 ° C. to 80 ° C. is used. In this case, if the glass transition temperature is less than the lower limit, the strength of the formed film is insufficient and the mechanical durability is poor. On the other hand, when the amount exceeds the upper limit, the solubility of the resin becomes low, the insoluble content of the resin remains, and the image characteristics are deteriorated, and peeling and cracks are likely to occur during the formation of the charge transport layer.

A polycarbonate resin, a polyarylate resin, a polyetherketone resin, an epoxy resin, a urethane resin, a cellulose ether, and those resins are constituted as the first binder resin having a glass transition temperature of 130 ° C. or more and 200 ° C. or less. Examples thereof include copolymers of monomers required. Considering stable electrical properties, mechanical strength, and manufacturing cost of the photoreceptor, it is preferable to repeat a polycarbonate resin having a viscosity average molecular weight of 30,000 to 50,000, a copolymer of polycarbonate resin, or a polycarbonate resin and a monomer of the resin. It is a copolymer as a component.

The polycarbonate resin used in the present invention can be generally obtained by a known method in which a dihydric phenol and phosgene are subjected to a polymerization reaction and the end is blocked with a monofunctional compound.

Specific examples of the dihydric phenol include 4,
4 '-(1-methylethylidene) bisphenol, 4,4'-(1-methylethylidene) bis [2-methylphenol], 4,4'-cyclohexylidene bisphenol, 4,4'-ethylidenebisphenol, 4, 4'-Propylidene bisphenol, 4,4 '
-Butylidene bisphenol, 4,4 '-(1,3-dimethylbutylidene) bisphenol, 4,4'-(1-methylethylidene) bis
[2,6-Dimethylphenol], 4,4 '-(1-phenylethylidene) bisphenol, 4,4'-(2-Ethylhexylidene) bisphenol, 5,5 '-(1-Methylethylidene) [1 , 1'-biphenyl] -2-ol, [1,1'-biphenyl] -4,4'-diol,
4,4'-methylidene bisphenol, 4,4'-methylenebis
[2- (2-propenyl) phenol, 4,4'-methylenebis [2-
Methyl phenol], 4,4'-propanediyl bisphenol, 4,4 '-(1-methylpropylidene) bisphenol,
4,4 '-(2-methylpropylidene) bisphenol, 4,4'-(3
-Methylbutylidene) bisphenol, 4.4'-cyclopentylidene bisphenol, 4,4 '-(phenylmethylidene)
Bisphenol, 4,4 '-(1-Methylheptylidene) bisphenol, 4,4'-Cyclohexylidenebis [3-methylphenol], 4,4'-(1-Methylethylidene) bis [2- (2 -Propenyl) phenol], 4,4 '-(1-methylethylidene) bis [2-
(1-methylethyl) phenol], 4,4 '-(1-methyloctylidene) bisphenol, 4,4'-(1-phenylethylidene)
Bis [2-methylphenol], 4,4'-cyclohexylidenebis [2,6-dimethylphenol], 4,4 '-(1-methyl) nonylidenebisphenol, 4,4'-decylidenebisphenol, 4, 4 '-(1-Methylethylidene) bis [2- (1,1-methylpropyl) phenol, 4,4'-(1-Methylethylidene) bis [2
-(1,1-Dimethylethyl) phenol, 4,4 '-(diphenylmethylidene) bisphenol, 4,4'-cyclohexylidenebis [2- (1,1-dimethylethyl) phenol], 4,4' -(2-
Methylpropylidene) bis [3-methyl-6- (1,1-dimethylethyl) phenol], 4,4 '-(1-methylethylidene) bis [2-
Cyclohexyl phenol], 4,4'-methylene bis [2,6
-Bis (1,1-dimethylethyl) phenol], 4,4'-methylenebis [2,6-di-sec-butylphenol], 5,5 '-(1,1-cyclohexylidene) bis- (1 , 1'-biphenyl) -2-ol,
4,4'-Cyclohexylidenebis [2-cyclohexylphenol], 2,2'-Methylenebis [4-nonylphenol],
4,4 '-(1-Methylethylidene) bis [2,6-bis (1,1-dimethylethyl) phenol], 5,5'-(1-phenolethylidene) [1,1'-biphenyl] -2 -Ol, bis (4-hydroxyphenyl) methanone, 4,4'-methylenebis [2-fluorophenol], 4,4 '-[2,2,2-trifluoro-1- (trifluoromethyl) ethylidene] bisphenol , 4,4'-isopropylidene bis [2-fluorophenol], 4,4 '-[(4-fluorophenyl) methylene] bis [2-fluorophenol], 4,
4 '-(phenylmethylene) bis [2-fluorophenol],
4,4 '-[(4-fluorophenyl) methylene] bisphenol,
4,4 '-(1-Methylethylidene) bis [2-chloro-6-methylphenol], 4,4'-(1-Methylethylidene) bis [2,6-dichlorophenol], 4,4 '-( 1-methylethylidene) bis [2-
Chlorophenol], 4,4'-methylenebis [2,6-dibromophenol], 4,4 '-(1-methylethylidene) bis [2,6-dibromophenol], 4,4'-(1-methylethylidene) ) Screw [2
-Nitrophenol], 3,3'-dimethyl- [1,1'-biphenyl] -4,4'-diol, 3,3'5,5'-Tetramethyl- [1,1'-biphenyl] -4 , 4'-diol, 3,3'5,5'-tetra-t-butyl-
[1,1'-Biphenyl] -4,4'-diol, 3,3'-difluoro-
Examples include [1,1′-biphenyl] -4,4′-diol and 3,3′5,5′-tetrafluoro- [1,1′-biphenyl] -4,4′-diol. Moreover, the glass transition temperature of the polymer having one of these as one of the monomers may be used in combination of two or more as long as it is 130 ° C. or higher and 200 ° C. or lower. Particularly from the viewpoint of reactivity, 4,4 '-(1-methylethylidene) bisphenol,
4,4'-Cyclohexylidene bisphenol is preferred.

As the second binder resin having a glass transition temperature of 0 ° C. or higher and 80 ° C. or lower, for example, polyester resin or methacrylic acid ester composed of an aromatic dicarboxylic acid component represented by polyethylene terephthalate and a glycol component is used. Examples of the copolymer include an acrylic resin containing a non-functional monomer such as the above as a main component and a functional monomer having a functional group such as a carboxyl group or a hydroxyl group, and a monomer of the resin. In particular, a polyester resin having a viscosity average molecular weight of 20,000 to 50,000 or a viscosity average molecular weight of 50,000 to 80,
It is preferable to use 000 acrylic resin in consideration of electric characteristics and image characteristics when repeatedly used, and manufacturing cost of the photoconductor.

Further, a resin obtained by blending the first resin and the second resin in an arbitrary ratio is used. In this case, the second binder resin is used as the binder resin of the charge transport layer in an amount of 5% by weight.
To 40% by weight is preferable.
If the ratio of the second binder resin is out of the above range, 5
If it is less than 10% by weight, the residual potential after repeated use tends to increase, and if it exceeds 40% by weight, the charging potential at repeated use tends to decrease.

Examples of the solvent include halogen solvents such as dichloromethane and 1,2-dichloroethane, ketones such as acetone, methyl ethyl ketone and cyclohexanone, ethyl acetate,
It is possible to use esters such as butyl acetate, ethers such as tetrahydrofuran and dioxane, aromatic hydrocarbons such as benzene, toluene and xylene, and aprotic polar solvents such as N, N-dimethylformamide and dimethyl sulfoxide. .

The film thickness is 5 to 50 μm, preferably 10 to 40 μm.

An antioxidant may be added as an additive to the charge generation layer or the charge transport layer. As the antioxidant, vitamin E, hydroquinone, hindered amine, hindered phenol, paraphenylenediamine, arylalkanes and their derivatives, organic sulfur compounds, organic phosphorus compounds and the like are used.

The temperature for drying the photoconductor is from 30 ° C. to 12
It is 0 ° C., and particularly preferably in the range of 80 ° C. to 100 ° C. If the drying temperature of the photoconductor is less than 80 ° C, the drying time becomes long, and if it is less than 30 ° C, it is difficult to sufficiently dry the photoconductor. Further, if the drying temperature exceeds 100 ° C., the electrical characteristics during repeated use tend to deteriorate, and if it exceeds 120 ° C., the image also deteriorates.

Further, in the case of producing a laminated type electrophotographic photoreceptor on the drum-shaped conductive support by the dip coating method, the binder resin concentration in the charge transport layer coating solution is 7% by weight to 13% by weight. And preferably 9 to 11% by weight. When the binder resin concentration is less than 9% by weight, the viscosity of the coating liquid is low, and it is necessary to increase the pulling speed of the drum to obtain a uniform film thickness. When the binder resin concentration is less than 7% by weight, the viscosity becomes lower, and it is difficult to obtain a uniform film thickness. On the other hand, if it exceeds 11% by weight, the viscosity of the coating liquid becomes high and it is necessary to slow down the speed of pulling up the drum in order to obtain a uniform film thickness. If it exceeds 13% by weight, a uniform film thickness cannot be obtained at a practical speed in the manufacturing process because of high viscosity, which is unsuitable in consideration of the manufacturing of the drum.

[0041]

According to the present invention, the glass transition temperature of the first resin blended as the binder resin is 130 ° C. to 200 ° C., and the glass transition temperature of the second resin is 0 ° C. to 80 ° C. By the following, the problem that the strength of the film is insufficient when the glass transition temperature is less than 0 ° C. and the mechanical durability is poor, and the dissolution of the resin that occurs when the glass transition temperature is higher than 200 ° C. Therefore, it is possible to solve the problems that the resin becomes insoluble, the insoluble content of the resin remains, the image characteristics are deteriorated, and peeling and cracks easily occur during the formation of the charge transport layer.

In the third aspect, the first resin constituting the binder resin is a polycarbonate resin or a polyarylate resin having a viscosity average molecular weight of 30,000 to 50,000, so that stable electrical characteristics and mechanical properties can be obtained. It is possible to obtain the desired strength and the desired manufacturing cost of the photoreceptor.

In the fourth aspect, the second resin constituting the binder resin has a viscosity average molecular weight of 20,000.
To 40,000 or a polyester resin having a viscosity average molecular weight of 50,000 to 80,000 makes it possible to obtain electrical characteristics and image characteristics during repeated use, and desirable manufacturing costs.

In the fifth or sixth aspect of the present invention, the binder resin concentration in the coating solution is set to 7% by weight or more and 13% by weight or less, whereby the coating liquid produced when the binder resin concentration is less than 7% by weight. Since the viscosity is low and it is difficult to obtain a uniform film thickness, and the high viscosity that occurs when the binder resin concentration is higher than 13% by weight, a uniform film thickness is obtained at a practical speed in the manufacturing process. It is possible to solve the problem that it cannot be obtained and is not suitable in consideration of the manufacturing of the drum.

[0045]

EXAMPLES The present invention will be described in detail below with reference to examples and comparative examples, but the present invention is not limited to the following examples as long as the gist thereof is not exceeded.

<Example 1>

[0047]

Embedded image

2 parts by weight of a bisazo pigment, which is a charge generating material represented by the above structural formula (Formula 1), and a phenoxy resin (PKH).
(H: manufactured by Union Carbide Co.) 1 part by weight and 97 parts by weight of 1,4-dioxane are dispersed by a ball mill disperser for 12 hours to prepare a dispersion liquid, which is filled in a tank and has a diameter of 8
An aluminum cylindrical support (aluminum drum) having a length of 0 mm and a length of 348 mm was immersed, lifted and coated, and dried at room temperature for 1 hour to form a charge generation layer having a thickness of 1 μm.

[0049]

Embedded image

On the other hand, 100 parts by weight of the hydrazone compound represented by the above structural formula (Formula 2) as a charge transport material, and a polycarbonate resin having a viscosity average molecular weight of 38,000 as a binder resin (C-1400: manufactured by Teijin Chemicals Ltd .; glass 80 parts by weight of transition temperature Tg = 157 ° C. and 20 parts by weight of polyester resin having a viscosity average molecular weight of 22,000 (V-290: manufactured by Toyobo Co., Ltd .; glass transition temperature Tg = 70 ° C.)
Dissolve in 800 parts by weight of dichloromethane to prepare a coating solution for coating the charge transport layer, dip-coat on the charge generating layer formed above, dry for 1 hour at 80 ° C., and transport the charge with a thickness of 20 μm. Layers were formed to prepare a sample as shown in FIG. The sample produced in this manner had a uniform coating film, and peeling of the photoreceptor did not occur.

A commercially available copying machine (SF887) was used for this sample.
(0: manufactured by Sharp Corporation), and a copy test was performed using A4 size paper. Image characteristics, charge potential (V0), and residual potential (Vr) were measured at the initial stage and after 40,000 times of use. The results are shown in Table 1. Beautiful images were obtained both in the initial stage and after repeated use. Further, no change in charging characteristics such as an increase in residual potential was observed, and there was almost no decrease in sensitivity due to a decrease in film thickness due to abrasion.

[0052]

[Table 1]

Example 2 As a binder resin, a polycarbonate resin having a viscosity average molecular weight of 39,000 (Z-4
00: Mitsubishi Gas Chemical Co., Ltd .; Tg = 182 ° C.) 60 parts by weight and viscosity average molecular weight 29,000 polyester resin (V
-103: manufactured by Toyobo Co., Ltd .; Tg = 48 ° C.) was prepared and evaluated in the same manner as in Example 1 except that 40 parts by weight of the photosensitive layer was dried at 70 ° C. No peeling of the photoreceptor was observed, and a uniform coating film was formed. The results are shown in Table 1. Beautiful images were obtained both in the initial stage and after repeated use. No change in charging characteristics such as increase in residual potential was observed, and there was almost no decrease in sensitivity due to reduction in film thickness due to abrasion.

Example 3 Polycarbonate having a viscosity average molecular weight of 39,000 (Z-40 as a binder resin)
0: Mitsubishi Gas Chemical Co .; Tg = 182 ° C.) 55 parts by weight and viscosity average molecular weight 22,000 polyester resin (V-
290: manufactured by Toyobo Co., Ltd .; Tg = 70 ° C.) was prepared and evaluated in the same manner as in Example 1 except that 45 parts by weight was used. The results are shown in Table 1.
Shown in A beautiful image was obtained in the early stage. However, after repeated use, a slight decrease in charging potential was seen,
No change was seen in the image.

Example 4 As a binder resin, a polycarbonate resin having a viscosity average molecular weight of 38,000 (C-1
400: manufactured by Teijin Chemicals; Tg = 157 ° C.) 40 parts by weight and a polyarylate resin (U having a viscosity average molecular weight of 43,000)
-100D: manufactured by Unitika Ltd .; Tg = 199 ° C.) 40 parts by weight, and a polyester resin having a viscosity average molecular weight of 21,000 (V-200: manufactured by Toyobo Co., Ltd .; Tg = 69 ° C.), 20 parts by weight, and the sample is 100 ° C. It was prepared and evaluated in the same manner as in Example 1 except that it was dried in. The results are shown in Table 1. No peeling of the photoreceptor was observed, and a uniform coating film was formed. A clear image was obtained both in the initial stage and after repeated use, no change was observed in the charging characteristics such as an increase in residual potential, and there was almost no decrease in sensitivity due to reduction in film thickness due to abrasion.

<Example 5> 4, as a binder resin
4 '-(1-methylethylidene) bisphenol and 4,
Viscosity average molecular weight 45,0 synthesized by copolymerizing 4 ′-(1-cyclohexylidene) bisphenol at 6: 4
The sample was dried at 120 ° C. by using 90 parts by weight of a polycarbonate resin of 00 (Tg = 148 ° C.) and 10 parts by weight of a polyester resin (V-290: manufactured by Toyobo Co., Ltd .; Tg = 70 ° C.) having a viscosity average molecular weight of 22,000. Others are Example 1
It produced similarly to and evaluated. The results are shown in Table 1. No peeling of the photoreceptor was observed, and a uniform coating film was formed. A clear image was obtained both in the initial stage and after repeated use, no change was observed in the charging characteristics such as an increase in residual potential, and there was almost no decrease in sensitivity due to reduction in film thickness due to abrasion.

Example 6 As a binder resin, a polycarbonate having a viscosity average molecular weight of 30,000 (K-130
0: Teijin Chemicals Co .; Tg = 152 ° C.) 95 parts by weight and 5 parts by weight of an acrylic resin having a viscosity average molecular weight of 65,000 (Dianal BR-64: Mitsubishi Rayon Co .; Tg = 55 ° C.) It was prepared and evaluated in the same manner as in Example 1. The results are shown in Table 1. No peeling of the photoreceptor was observed, and a uniform coating film was formed. A clear image was obtained both in the initial stage and after repeated use, no change was observed in the charging characteristics such as an increase in residual potential, and there was almost no decrease in sensitivity due to reduction in film thickness due to abrasion.

Example 7 Polycarbonate having a viscosity average molecular weight of 39,000 (Z-40 as a binder resin)
0: Mitsubishi Gas Chemical Co., Ltd .; Tg = 182 ° C.) 80 parts by weight and an acrylic resin having a viscosity average molecular weight of 60,000 (Dianal BR-107: Mitsubishi Rayon Co .; Tg = 50 ° C.)
It was prepared and evaluated in the same manner as in Example 1 except that 20 parts by weight was used. The results are shown in Table 1. No peeling of the photoreceptor was observed, and a uniform coating film was formed. A clear image was obtained both in the initial stage and after repeated use, no change was observed in the charging characteristics such as an increase in residual potential, and there was almost no decrease in sensitivity due to reduction in film thickness due to abrasion.

Comparative Example 1 Polycarbonate resin having a viscosity average molecular weight of 38,000 (C-1
400: manufactured by Teijin Chemical Co., Ltd .; Tg = 157 ° C.) and produced and evaluated in the same manner as in Example 1 except that only 100 parts by weight was used.
The results are shown in Table 1. A beautiful image was obtained in the early stage.
However, when used repeatedly, white streaks were generated at the edges of the image.

Comparative Example 2 As a binder resin, a polycarbonate resin having a viscosity average molecular weight of 38,000 (C-1
400: Teijin Chemical Co .; Tg = 157 ° C.) 70 parts by weight and viscosity average molecular weight 120,000 synthesized from 4,4 ′-(1-methylethylidene) bisphenol (BPA)
Example 3 was prepared and evaluated in the same manner as in Example 1 except that 30 parts by weight of the polycarbonate resin (Tg = 161 ° C.) in Example 1 was used. The results are shown in Table 1. A uniform solution was not formed from the time of the coating liquid for coating the charge transport layer, and spots that appeared to be insoluble matter of the resin were generated on the photoconductor from the initial stage, and were black spots in the image.

Comparative Example 3 Viscosity average molecular weight 4 synthesized from bisphenol A and phthalic acid as binder resin
5,000 polyarylate resin (Tg = 207 ° C.) 1
It was prepared and evaluated in the same manner as in Example 1 except that 100 parts by weight was used. The results are shown in Table 1. A clear image was obtained in the initial stage, but a decrease in charging potential was observed after repeated use,
The image density became much lighter than the initial one.

Comparative Example 4 A polyester resin (V-10 having a viscosity average molecular weight of 29,000) was used as a binder resin.
(3: manufactured by Toyobo Co., Ltd .; Tg = 48 ° C.) was prepared and evaluated in the same manner as in Example 1 except that 100 parts by weight was used. The results are shown in Table 1. A clear image was obtained in the initial stage, but when repeatedly used, the charge potential decreased, and the image density became extremely thin compared to the initial stage.

<Comparative Example 5> 4, as a binder resin
80 parts by weight of a polycarbonate resin (Tg = 126 ° C.) having a viscosity average molecular weight of 43,000 synthesized from 4 ′-(1-methylethylidene) bis [2-methylphenol], and a polyester resin having a viscosity average molecular weight of 21,000 (V -200: manufactured by Toyobo Co., Ltd .; Tg = 69 ° C.) Example 1 except that 20 parts by weight was used and the sample was dried at 100 ° C.
It produced similarly to and evaluated. The results are shown in Table 1. No peeling of the photoreceptor was observed, and a uniform coating film was formed. A clear image was obtained in the initial stage, but after repeated use, the residual potential increased and the image density became much higher than in the initial stage, causing fog on the white background.

Comparative Example 6 A polycarbonate resin having a viscosity average molecular weight of 39,000 (Z-4 was used as a binder resin.
00: Mitsubishi Gas Chemical Co., Ltd .; Tg = 182 ° C.) 70 parts by weight and acrylic resin having a viscosity average molecular weight of 90,000 (Dianal BR-75: Mitsubishi Rayon Co .; Tg = 85 ° C.)
Using 30 parts by weight, the sample was prepared and evaluated in the same manner as in Example 1 except that the sample was dried at 120 ° C. The results are shown in Table 1. A slight peeling was observed at the end of the photoconductor and a crack was generated on the surface, and an increase in residual potential was observed after repeated use.

Comparative Example 7 As a binder resin, a polycarbonate resin having a viscosity average molecular weight of 38,000 (C-1
400: Teijin Chemical Co .; Tg = 157 ° C.) 90 parts by weight,
And viscosity average molecular weight 5 synthesized from ethyl acrylate
5,000 polyacrylic resin (Tg = -21 ° C) 10
The parts were prepared and evaluated in the same manner as in Example 1 except that parts by weight were used and the sample was dried at 90 ° C. The results are shown in Table 1. No peeling of the photoreceptor was observed, and a uniform coating film was formed. A clear image was obtained in the initial stage, but after repeated use, the residual potential increased and the image density became much higher than in the initial stage, causing fog on the white background.

Example 8 Copolymerized nylon (Amilan C
M8000: manufactured by Toray) 6 parts by weight of methyl alcohol 4
Dissolve in a mixed solvent of 7 parts by weight and 47 parts by weight of chloroform, and fill the tank with this, and the diameter is 30 mm and the length is 255 mm.
Immersing, pulling up and coating the aluminum cylindrical support of 11
It was dried at 0 ° C. for 10 minutes to provide an undercoat layer of about 2 μm.

[0067]

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Next, 2 parts by weight of an X-type metal-free phthalocyanine, which is a charge generating material represented by the above structural formula (Formula 3), and a polyvinyl butyral resin (S-REC BMS: manufactured by Sekisui Chemical Co., Ltd.)
1 part by weight and 97 parts by weight of dichloroethane were dispersed by a ball mill disperser for 12 hours to prepare a dispersion liquid, which was filled in a tank, and the aluminum cylindrical support having the above-mentioned undercoat layer was dipped and pulled up. The coating was performed and dried at room temperature for 1 hour to form a charge generation layer having a thickness of 0.2 μm.

[0069]

[Chemical 4]

On the other hand, 100 parts by weight of the styryl compound represented by the above structural formula (Formula 4) as a charge transport material and a polycarbonate resin having a viscosity average molecular weight of 30,000 as a binder (K-1300: manufactured by Teijin Chemicals; Tg = 152).
C) 80 parts by weight and a polyester resin having a viscosity average molecular weight of 29,000 (V-103: manufactured by Toyobo Co., Ltd .; Tg = 48 ° C.)
20 parts by weight of chloroform is dissolved in 800 parts by weight of chloroform to prepare a coating solution for coating the charge transport layer, which is applied by dip coating on the charge generating layer formed above and dried at 100 ° C. for 1 hour to give a thickness. A 20 μm charge transport layer was formed. The sample thus produced had a uniform coating film. This sample was mounted on a commercially available laser beam printer (JX9500: manufactured by Sharp Corporation). The results are shown in Table 1. A clear image was obtained both in the initial stage and after repeated use, there was almost no change in charging characteristics such as increase in residual potential, and almost no decrease in sensitivity due to film thickness reduction due to abrasion.

<Example 9>

[0072]

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2 parts by weight of the bisazo pigment which is the charge generating material represented by the above structural formula (Formula 5), 1 part by weight of polyvinyl butyral resin (XYHL: manufactured by Union Carbide Co.) and 97 parts by weight of cyclohexanone are dispersed by a ball mill to prepare a dispersion liquid. Was prepared, the tank was filled with this, and an anodized layer was provided by anodization to have a thickness of 5 μm. The diameter was 80 mm and the length was 348.
It was applied by dip coating on an aluminum cylindrical support having a thickness of 10 mm and dried at 110 ° C. for 10 minutes to form a charge generation layer having a thickness of 0.8 μm.

[0074]

[Chemical 6]

On the other hand, 100 parts by weight of the hydrazone compound represented by the above structural formula (Formula 6) as a charge transport material and a polycarbonate resin having a viscosity average molecular weight of 39,000 as a binder (Z-400: manufactured by Mitsubishi Gas Chemical Co .; Tg = 1
82 ° C.) 70 parts by weight and 30 parts by weight of an acrylic resin having a viscosity average molecular weight of 70,000 (Dianal BR-79: manufactured by Mitsubishi Rayon Co .; Tg = 35 ° C.) are added to dichloromethane 800 parts.
It is dissolved in 1 part by weight to prepare a coating solution for coating the charge transport layer, which is applied by dip coating on the charge generating layer formed above, and then at 80 ° C. for 1 hour.
Drying was performed for an hour to form a charge transport layer having a thickness of 25 μm. The sample thus produced had a uniform coating film.
Evaluation was performed in the same manner as in Example 1. The results are shown in Table 1. A clear image was obtained both in the initial stage and after repeated use, the change in the charging characteristics such as the increase in the residual potential was small, and the decrease in the sensitivity due to the decrease in the film thickness due to abrasion was hardly seen.

<Example 10 (sheet type photoreceptor)>

[0077]

[Chemical 7]

2 parts by weight of the perylene pigment which is the charge generating material represented by the above structural formula (Formula 7) and the phenoxy resin (PKH
H: manufactured by Union Carbide Co., Ltd.) 1 part by weight and 97 parts by weight of 1,4-dioxane are dispersed by a ball mill disperser for 12 hours to prepare a dispersion liquid, and an aluminum layer is formed on the surface of polyethylene terephthalate by a vapor deposition method. The formed electroconductive support was coated with an applicator and dried at room temperature to form a charge generation layer having a thickness of 1 μm.

[0079]

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On the other hand, 100 parts by weight of the triphenylamine compound represented by the above structural formula as the charge transport material and 4,4 '-(1-methylethylidene) bis [2-methylphenol] and 4,4'- as the binder. 80 parts by weight of a polycarbonate resin (Tg = 148 ° C.) having a viscosity average molecular weight of 43,000 synthesized by copolymerizing (1-cyclohexylidene) bisphenol with 51:49 and a polyester resin having a viscosity average molecular weight of 22,000 (V- 290: Mitsubishi Gas Chemical Co., Ltd .; Tg = 70 ° C.) 20 parts by weight and dimethyl silicone oil (SH200 50 cs: manufactured by Toray Silicone Co., Ltd.) 0.02 parts by weight are dissolved in 800 parts by weight of dichloromethane and applied for coating the charge transport layer. A liquid is prepared and coated on the charge generation layer formed above with an applicator,
Drying was carried out at 80 ° C. for 1 hour to form a charge transport layer having a thickness of 25 μm. The sample thus produced had a uniform coating film. This sample was attached to a cylindrical support made of aluminum having a diameter of 80 mm and a length of 348 mm with a conductive tape and mounted on a commercially available copying machine (SF8870: manufactured by Sharp Corporation).
Evaluation was performed in the same manner as in Example 4. The results are shown in Table 1. A clear image was obtained both in the initial stage and after repeated use, and there was almost no reduction in sensitivity due to the reduction in film thickness due to abrasion.

<Example 11 (Function-separated photoconductor)>

[0082]

[Chemical 9]

Using a paint shaker, 2 parts by weight of a bisazo pigment, which is the charge generating material represented by the above structural formula (Formula 9), 1 part by weight of an epoxy resin (Rikaresin BPO-20E: manufactured by Shin Nippon Rika Co., Ltd.) and 97 parts by weight of dimethoxyethane are used. And dispersed for 6 hours to prepare a dispersion liquid. This is filled in a tank, and an aluminum cylindrical support (aluminum drum) having a diameter of 80 mm and a length of 348 mm is dipped, pulled up and coated, and dried at room temperature for 1 hour to form a charge generation layer having a thickness of 0.2 μm. did.

[0084]

[Chemical 10]

On the other hand, as a charge transport material, 100 parts by weight of the bishydrazone compound represented by the above structural formula (Formula 10) was used as a binder, and a polycarbonate resin having a viscosity average molecular weight of 38,000 (C-1400: manufactured by Teijin Chemical Co .; Tg =
157 ° C.) 90 parts by weight and viscosity average molecular weight 22,000 polyester resin (V-290: manufactured by Mitsubishi Gas Chemical Co., Ltd .; T
(g = 70 ° C.) 10 parts by weight is dissolved in 800 parts by weight of dichloromethane to prepare a coating solution for coating the charge transport layer, which is applied by dip coating on the charge generating layer formed above and dried at 80 ° C. for 1 hour. Then, a charge transport layer having a thickness of 25 μm was formed, and a sample as shown in FIG. 1 was prepared. The sample thus produced had a uniform coating film. This sample was evaluated in the same manner as in Example 1. The results are shown in Table 1. A clear image was obtained both in the initial stage and after repeated use, and even under high temperature and high humidity, changes in charging characteristics such as increase in residual potential were hardly seen, and there was almost no decrease in sensitivity due to film thickness reduction due to abrasion.

<Example 12 (single-layer type photoconductor)>

[0087]

[Chemical 7]

2 parts by weight of the perylene pigment, which is the charge generating material represented by the above structural formula, and 98 parts by weight of 1,2-dichloroethane were dispersed by a paint shaker to prepare a dispersion liquid.

[0089]

[Chemical 10]

100 parts by weight of the hydrazone compound represented by the above structural formula as a charge transport material and a polycarbonate resin having a viscosity average molecular weight of 39,000 as a binder (Z-
400: Mitsubishi Gas Chemical Co., Ltd .; Tg = 182 ° C.) 80 parts by weight and viscosity average molecular weight 22,000 polyester resin (V-290: Mitsubishi Gas Chemical Co., Ltd .; Tg = 70 ° C.) 20
A solution prepared by dissolving 1 part by weight in 700 parts by weight of dichloromethane was added to prepare a coating solution for coating a photosensitive layer, which was applied by dip coating on an aluminum cylindrical support and dried at 100 ° C. for 1 hour to give a thickness of 15 μm. The photosensitive layer of No. 1 was formed to prepare a photoconductor as shown in FIG. The sample thus produced had a uniform coating film. A commercially available copying machine (SF810
(0: manufactured by Sharp Corporation) was mounted on an experimental machine modified for positive charging, and evaluated in the same manner as in Example 4. Table 2 shows the results. A clear image was obtained both in the initial stage and after repeated use, and there was almost no reduction in sensitivity due to the reduction in film thickness due to abrasion.

Example 13 (Single-Layer Photoreceptor Provided with Undercoat Layer) 6 parts by weight of methoxymethylated nylon (EF-30T: manufactured by Teikoku Kagaku Co.) was added with 47 parts by weight of methyl alcohol and 1,2-dichloroethane. Dissolve in 47 parts by weight of mixed solvent, fill the tank with it, diameter 80 mm, length 348 m
1. Immerse, pull up and coat 1 m of aluminum cylindrical support
It was dried at 10 ° C. for 10 minutes to provide an undercoat layer of about 1 μm.

[0092]

[Chemical 7]

2 parts by weight of the perylene pigment, which is the charge generating material represented by the above structural formula, and 98 parts by weight of 1,2-dichloroethane were dispersed with a paint shaker to prepare a dispersion liquid.

[0094]

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100 parts by weight of the hydrazone compound represented by the above structural formula as a charge transport material and a polycarbonate resin having a viscosity average molecular weight of 39,000 (Z-
400: Mitsubishi Gas Chemical Co., Ltd .; Tg = 182 ° C.) 80 parts by weight and viscosity average molecular weight 22,000 polyester resin (V-290: Mitsubishi Gas Chemical Co., Ltd .; Tg = 70 ° C.) 20
A solution prepared by dissolving 1 part by weight in 700 parts by weight of dichloromethane was added to prepare a coating solution for coating the photosensitive layer, which was applied by dip coating on the aluminum cylindrical support provided with the undercoat layer at 100 ° C.
And dried for 1 hour to form a photosensitive layer having a thickness of 15 μm. The sample thus produced had a uniform coating film.
This sample was mounted on a commercially available copying machine (SF8100: manufactured by Sharp Corporation) which was modified for positive charging, and evaluated in the same manner as in Example 1. A clear image was obtained both in the initial stage and after repeated use, and there was almost no reduction in sensitivity due to the reduction in film thickness due to abrasion.

Example 14 The procedure of Example 10 was repeated, except that the coating solution for coating the charge transport layer contained 600 parts by weight of dichloromethane. The coating solution had a high viscosity, but a uniform film thickness could be obtained by slowing the pulling rate.

Example 15 In addition to 1000 parts by weight of dichloromethane used in the coating liquid for coating the charge transport layer,
It was prepared and evaluated in the same manner as in Example 10. Although the coating liquid had a low viscosity, a uniform film thickness could be obtained by increasing the pulling speed.

Comparative Example 8 The same preparation and evaluation as in Example 10 were carried out except that the amount of dichloromethane used in the coating liquid for coating the charge transport layer was changed to 500 parts by weight. The coating liquid had a very high viscosity and could not be formed into a uniform film thickness, and the image had uneven density over the entire image.

Comparative Example 9 The procedure of Example 16 was repeated except that the amount of dichloromethane used in the coating liquid for coating the charge transport layer was changed to 1100 parts by weight. The coating liquid had a very low viscosity and could not have a uniform film thickness, and only a charge transport layer having a film thickness of 10 μm was obtained.

[0100]

According to the electrophotographic photosensitive member of claim 1 or 2, the compatibility of the charge transporting material used in the photosensitive layer or the charge transporting layer with the binder resin and the binder resin, the viscosity of the coating solution, and the photosensitivity. Problems related to delamination of the body and cracks and the occurrence of cracks can be solved at the same time.

According to the electrophotographic photosensitive member of claim 3 or 4, the electrophotographic photosensitive member exhibiting stable electric characteristics, which suppresses a decrease in charging potential and an increase in residual potential even when repeatedly used, has good durability. You can get the body.

According to the method of manufacturing the electrophotographic photosensitive member of claim 5 or 6, it is possible to manufacture the drum with high accuracy, and it is possible to suppress the peeling of the photosensitive layer, the occurrence of cracks and the like. .

[Brief description of drawings]

FIG. 1 is a schematic cross-sectional view showing an example of a photoconductor of the present invention.

FIG. 2 is a schematic cross-sectional view showing an example of the photoconductor of the present invention.

FIG. 3 is a schematic cross-sectional view showing an example of the photoconductor of the present invention.

[Explanation of symbols]

 DESCRIPTION OF SYMBOLS 1 Conductive support 2 Charge generation layer 3 Charge transport layer 4 Photosensitive layer 5 Intermediate layer 6 Charge generation material

Claims (6)

[Claims] 1. An electrophotographic photosensitive member comprising a conductive support and a photosensitive layer formed on the conductive support and containing at least a charge-generating substance and a charge-transporting substance. The binder resin contained in the photosensitive layer is 130. A first resin having a glass transition temperature of not less than 200 ° C and not more than 200 ° C,
An electrophotographic photoreceptor, which is a resin blended with a second resin having a glass transition temperature of 0 ° C. or higher and 80 ° C. or lower. 2. A laminated electrophotographic photosensitive member comprising a conductive support, on which a charge generating layer containing at least a charge generating substance and a charge transporting layer containing a charge transporting substance are independently function-separated. In the above, the binder resin of the charge transport layer is 130 ° C. or higher and 20
A first resin having a glass transition temperature of 0 ° C. or lower, and 0 ° C.
An electrophotographic photoreceptor comprising a resin blended with a second resin having a glass transition temperature of 80 ° C. or lower. 3. The first resin constituting the binder resin is a polycarbonate resin or a polyarylate resin having a viscosity average molecular weight of 30,000 or more and 50,000 or less, and the first resin is a polyarylate resin. The electrophotographic photosensitive member according to 1. 4. The second resin constituting the binder resin is a polyester resin having a viscosity average molecular weight of 20,000 or more and 40,000 or less, or an acrylic resin having a viscosity average molecular weight of 50,000 or more and 80,000 or less. The electrophotographic photosensitive member according to claim 1, 2 or 3, which is characterized in that. 5. A method for producing an electrophotographic photosensitive member comprising a drum-shaped conductive support and a photosensitive layer containing at least a charge generating substance and a charge transporting substance immersed in the photosensitive layer coating solution. Binder resin concentration is 7% by weight
The amount is 13% by weight or less and the method for producing an electrophotographic photosensitive member according to claim 1, wherein the amount is 13% by weight or less. 6. A stack type electron comprising a drum-shaped conductive support and a charge generation layer containing at least a charge generation substance and a charge transport layer containing a charge transport substance, which are independently immersed in each other. In the method for producing a photographic photoreceptor, the binder resin concentration in the charge transport layer coating liquid is 7% by weight.
3. The method for producing an electrophotographic photosensitive member according to claim 2, wherein the content is 13% by weight or less.