JP4453548B2 - Electrophotographic photosensitive member, process cartridge, and image forming apparatus - Google Patents

Description

  The present invention relates to an electrophotographic photosensitive member, a process cartridge, and an image forming apparatus.

  A so-called xerographic image forming apparatus includes an electrophotographic photosensitive member, a charging device, an exposure device, a developing device, and a transfer device, and performs image formation by an electrophotographic process using them.

  2. Description of the Related Art In recent years, xerographic image forming apparatuses have been further improved in speed and life due to technological progress of each member and system. Accordingly, demands for high-speed compatibility and high reliability of each subsystem are higher than ever. In particular, there is a strong demand for high-speed compatibility and high reliability for a photoconductor used for image writing and a cleaning member for cleaning the photoconductor. In addition, the photosensitive member and the cleaning member receive more stress than the other members due to their mutual sliding. Therefore, in order to prevent image defects, it is desirable to suppress the occurrence of scratches and wear on the photoreceptor.

  Therefore, the conventional electrophotographic photosensitive member has a long life by using a resin having high mechanical strength. An example of such a resin is an epoxy resin (see, for example, Patent Documents 1 and 2).

JP-A-56-51749 JP-A-8-278645

  However, even with the photoconductors described in Patent Documents 1 and 2, scratches and wear cannot be sufficiently suppressed, and it has been difficult to obtain good image quality over a long period of time.

  The present invention has been made in view of the above circumstances, and an object thereof is to provide an electrophotographic photosensitive member capable of maintaining high image quality over a long period of time, and a process cartridge and an image forming apparatus using the same.

  In order to solve the above problems, an electrophotographic photoreceptor of the present invention comprises a conductive substrate and a photosensitive layer provided on the conductive substrate, and the photosensitive layer has a cross-linked structure on the side farthest from the conductive substrate. And an oxetane resin containing an oxetane compound as a resin component.

  According to the electrophotographic photoreceptor of the present invention, by having the outermost surface layer, an image forming apparatus capable of maintaining high image quality over a long period can be effectively realized. Although the reason why the above-described effect can be obtained by the present invention is not necessarily clear, the present inventors infer as follows.

Usually, in the image forming apparatus, with the electrophotographic process, discharge products such as NO _x and ozone gas is produced. This discharge product is considered not only to adhere to the surface of the photosensitive layer but also to penetrate into the photosensitive layer. In the conventional photoconductor, oxides are generated from unreacted hydroxyl groups present in the epoxy resin due to charging stress such as discharge products, which serve as carrier traps that hinder charge transport and have electrical characteristics. It is presumed that the mechanical strength of the epoxy resin was reduced as it adversely affected and caused deterioration of the resin. In contrast, in the electrophotographic photoreceptor of the present invention, the outermost surface layer containing the oxetane resin can be a cured film having a high crosslinking density, and the density of unreacted hydroxyl groups present in the resin as compared with the epoxy resin. It is presumed that by reducing the thickness of the photosensitive layer, the penetration of the discharge product into the photosensitive layer can be sufficiently suppressed, the generation of oxides is remarkably reduced, and the wear resistance can be sufficiently maintained over a long period of time.

In the electrophotographic photoreceptor of the present invention, the outermost surface layer has a charge having at least one functional group selected from a hydroxyl group, a carboxyl group, an alkoxysilyl group, an epoxy group, an oxetane group, a thiol group, and an amino group. the transport material further including. Note that these charge transport materials may be incorporated into the resin by reacting with the oxetane compound or the oxetane resin. Such an electrophotographic photoreceptor can more reliably realize an image forming apparatus capable of maintaining high image quality over a long period of time.

  Such an effect is that the functional group of the charge transport material reacts with an unreacted hydroxyl group of the oxetane resin in the formation process of the outermost surface layer, so that an oxetane resin having a sufficiently small residual hydroxyl group can be formed, and the charge transport The combination of the material and the oxetane compound further increases the cross-link density of the oxetane resin and further improves the wear resistance. Further, the combination of the charge transport material and the oxetane compound provides excellent electrical properties. It is thought that.

In the electrophotographic photoreceptor of the present invention, the charge transport material is selected from the compounds represented by the following general formula (I), (II) or (III) from the viewpoint of further improving charge transport properties and mechanical strength. It is preferable that it is at least one kind.
F-[(X ¹ ) _m ^1- (R ¹ ) _{m 2} -Y] _{m 3} (I)
In formula (I), F represents an organic group derived from a compound having a hole transporting ability, X ¹ represents an oxygen atom or a sulfur atom, R ¹ represents an alkylene group, Y represents a hydroxyl group, a carboxyl group, a thiol group, or An amino group, m1 and m2 each independently represent 0 or 1, and m3 represents an integer of 1 to 4;
_{^{F - [(X 2) n1}} - (R 2) n2 - (Z) n3 G] n4 (II)
In formula (II), F represents an organic group derived from a compound having a hole transporting ability, X ² represents an oxygen atom or a sulfur atom, R ² represents an alkylene group, Z represents an oxygen atom, a sulfur atom, NH or COO, G represents an epoxy group or oxetane group, n1, n2 and n3 each independently represents 0 or 1, and n4 represents an integer of 1 to 4.
F- [D-Si (R ³ ) _(3-a) Q _a ] _b (III)
In the formula (III), F represents an organic group derived from a compound having a hole transport ability, D represents a divalent group having flexibility, R ³ represents a hydrogen atom, a substituted or unsubstituted alkyl group, or A substituted or unsubstituted aryl group, Q is a hydrolyzable group, a is an integer of 1 to 3, and b is an integer of 1 to 4.

  In the electrophotographic photoreceptor of the present invention, the oxetane resin preferably further contains an epoxy compound as a resin component. As a result, the wear resistance of the photoreceptor can be further improved.

  Further, the oxetane resin preferably further contains a phenol derivative having a methylol group as a resin component. As a result, the abrasion resistance of the photoreceptor can be further improved, the cleaning property of the outermost surface layer is improved, the effect of suppressing the deterioration of the photosensitive layer due to the discharge product is improved, and the image quality is improved. It can be maintained more reliably.

  Conventionally, a protective layer containing a phenolic resin has a tendency to deteriorate in electrical characteristics due to being easily colored by oxidation and easily remaining water molecules. In addition, a phenol-epoxy resin in which a phenol derivative and an epoxy compound are combined is known as a cured resin. However, when this resin is applied to an electrophotographic photoreceptor, the compatibility with the charge transport material, electrical characteristics, Abrasion was insufficient, and high image quality was not yet achieved. On the other hand, the electrophotographic photosensitive member of the present invention combines the oxetane compound and the phenol derivative having a methylol group, thereby improving the antioxidant ability and improving the abrasion resistance, thereby further improving the cleaning property. It can be obtained, and it is considered that high image quality can be achieved more reliably.

  The image forming apparatus of the present invention also forms an electrostatic latent image by exposing any of the electrophotographic photosensitive members of the present invention, a charging device for charging the electrophotographic photosensitive member, and the charged electrophotographic photosensitive member. The image forming apparatus includes: an exposure device; a developing device that develops an electrostatic latent image to form a toner image; and a transfer device that transfers the toner image to a transfer target.

  Further, the process cartridge of the present invention includes any one of the electrophotographic photosensitive members of the present invention, a charging device for charging the electrophotographic photosensitive member, and a development that develops an electrostatic latent image formed by exposure to form a toner image. And at least one selected from a cleaning device for removing toner remaining on the electrophotographic photosensitive member.

  Since the image forming apparatus and the process cartridge of the present invention include the electrophotographic photosensitive member of the present invention, high image quality can be provided over a long period of time.

  According to the present invention, it is possible to provide an electrophotographic photosensitive member, a process cartridge, and an image forming apparatus that can maintain high image quality over a long period of time.

  Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings. In the description of the drawings, the same or corresponding elements are denoted by the same reference numerals, and redundant description is omitted.

<Electrophotographic photoreceptor>
FIG. 1 is a schematic cross-sectional view showing a preferred embodiment of the electrophotographic photosensitive member of the present invention. An electrophotographic photosensitive member 1 shown in FIG. 1 includes a conductive support 2 and a photosensitive layer 3. The photosensitive layer 3 has a structure in which an undercoat layer 4, a charge generation layer 5, and a charge transport layer 6 are laminated in this order on a conductive support 2. In the electrophotographic photoreceptor 1 shown in FIG. 1, the charge transport layer 6 is an outermost surface layer containing a resin having a crosslinked structure, and includes an oxetane resin containing an oxetane compound as a resin component.

  2 to 5 are schematic sectional views showing other preferred embodiments of the electrophotographic photosensitive member of the present invention. The electrophotographic photosensitive member shown in FIGS. 2 to 3 includes the photosensitive layer 3 in which the functions are separated into the charge generation layer 5 and the charge transport layer 6 as in the electrophotographic photosensitive member shown in FIG. 4 to 5 show that the charge generation material and the charge transport material are contained in the same layer (single-layer type photosensitive layer 8).

  The electrophotographic photoreceptor 1 shown in FIG. 2 has a structure in which an undercoat layer 4, a charge generation layer 5, a charge transport layer 6 and a protective layer 7 are sequentially laminated on a conductive support 2. The electrophotographic photoreceptor 1 shown in FIG. 3 has a structure in which an undercoat layer 4, a charge transport layer 6, a charge generation layer 5, and a protective layer 7 are sequentially laminated on a conductive support 2. In the electrophotographic photoreceptor 1 shown in FIGS. 2 and 3, the protective layer 7 is the outermost surface layer containing a resin having a crosslinked structure, and includes an oxetane resin containing an oxetane compound as a resin component.

  The electrophotographic photoreceptor 1 shown in FIG. 4 has a structure in which an undercoat layer 4 and a single-layer type photosensitive layer 8 are sequentially laminated on a conductive support 2. It is an outermost surface layer containing a resin having a crosslinked structure, and includes an oxetane resin containing an oxetane compound as a resin component.

  The electrophotographic photoreceptor 1 shown in FIG. 5 has a structure in which an undercoat layer 4, a single-layer type photosensitive layer 8, and a protective layer 7 are sequentially laminated on a conductive support 2. Is an outermost surface layer containing a resin having a crosslinked structure, and includes an oxetane resin containing an oxetane compound as a resin component. In the electrophotographic photoreceptor 1, the undercoat layer 4 is not necessarily provided.

  As described above, the photosensitive layer provided in the electrophotographic photosensitive member of the present invention is a single-layer type photosensitive layer containing a charge generation material and a charge transport material in the same layer, or a layer containing a charge generation material (charge generation material). Layer) and a layer containing a charge transport material (charge transport layer) may be any function-separated type photosensitive layer provided separately. In the case of the function-separated type photosensitive layer, any of the stacking order of the charge generation layer and the charge transport layer may be the upper layer. In the case of a function-separated photosensitive layer, it is possible to achieve functional separation because it is possible to perform functional separation in which each layer only has to satisfy each function.

  Hereinafter, each element will be described based on the electrophotographic photoreceptor 1 shown in FIG. 2 as a representative example.

  Examples of the conductive support 2 include a metal plate, a metal drum, and a metal belt formed using a metal or an alloy such as aluminum, copper, zinc, stainless steel, chromium, nickel, molybdenum, vanadium, indium, gold, or platinum. Etc. Further, as the conductive support 2, paper, plastic film, belt or the like coated, vapor-deposited or laminated with a conductive polymer, a conductive compound such as indium oxide, or a metal or alloy such as aluminum, palladium, or gold can be used.

  The surface of the conductive support 2 is preferably roughened to a centerline average roughness Ra of 0.04 μm to 0.5 μm in order to prevent interference fringes generated when laser light is irradiated. If Ra on the surface of the conductive support 2 is less than 0.04 μm, the effect of preventing interference tends to be insufficient because it is close to a mirror surface. On the other hand, if Ra exceeds 0.5 μm, the image quality tends to be insufficient even if a film is formed. When non-interfering light is used as a light source, it is not particularly necessary to roughen the interference fringes, and it is possible to prevent the occurrence of defects due to irregularities on the surface of the conductive support 2, which is suitable for longer life.

  Surface roughening methods include wet honing by suspending the abrasive in water and spraying it on the support, or centerless grinding and anodic oxidation in which the support is pressed against a rotating grindstone and continuously ground. Treatment etc. are preferred.

  As a roughening method, without roughening the surface of the conductive support 2, a conductive or semiconductive powder is dispersed in the resin, and a layer is formed on the surface of the support. A method of roughening with fine particles dispersed therein is also preferably used.

  The anodizing treatment is to form an oxide film on the aluminum surface by anodizing in an electrolyte solution using aluminum as an anode. Examples of the electrolyte solution include a sulfuric acid solution and an oxalic acid solution. However, the intact porous anodic oxide film is chemically active, easily contaminated, and has a large resistance fluctuation due to the environment. Therefore, the pores of the anodic oxide film are sealed with pressurized water vapor or boiling water (a metal salt such as nickel may be added) by volume expansion due to a hydration reaction, and a sealing process is performed to change to a more stable hydrated oxide. .

  The thickness of the anodized film is preferably 0.3 to 15 μm. If it is less than 0.3 μm, the barrier property against injection tends to be poor and the effect tends to be insufficient. On the other hand, when it exceeds 15 μm, there is a tendency that the residual potential increases due to repeated use.

  Further, the conductive support 2 may be subjected to treatment with an acidic aqueous solution or boehmite treatment. The treatment with an acidic treatment liquid comprising phosphoric acid, chromic acid and hydrofluoric acid is carried out as follows. First, an acidic treatment liquid is prepared. The mixing ratio of phosphoric acid, chromic acid and hydrofluoric acid in the acidic treatment liquid is such that phosphoric acid is in the range of 10 to 11% by mass, chromic acid is in the range of 3 to 5% by mass, and hydrofluoric acid is in the range of 0.5 to 2% by mass. The concentration of these acids is preferably in the range of 13.5 to 18% by mass. The treatment temperature is preferably 42 to 48 ° C., but by keeping the treatment temperature high, a thicker film can be formed faster. The film thickness is preferably 0.3 to 15 μm. If it is less than 0.3 μm, the barrier property against injection tends to be poor and the effect tends to be insufficient. On the other hand, when it exceeds 15 μm, there is a tendency that the residual potential increases due to repeated use.

  The boehmite treatment can be performed by immersing in pure water at 90 to 100 ° C. for 5 to 60 minutes, or by contacting with heated steam at 90 to 120 ° C. for 5 to 60 minutes. The film thickness is preferably 0.1 to 5 μm. This can be further anodized using an electrolyte solution with low film solubility such as adipic acid, boric acid, borate, phosphate, phthalate, maleate, benzoate, tartrate, citrate, etc. Good.

  The undercoat layer 4 is formed on the conductive support 2. The undercoat layer 4 includes an organometallic compound and / or a binder resin.

  As organometallic compounds, zirconium chelate compounds, zirconium alkoxide compounds, organozirconium compounds such as zirconium coupling agents, titanium chelate compounds, titanium alkoxide compounds, organotitanium compounds such as titanate coupling agents, aluminum chelate compounds, aluminum coupling agents In addition to organoaluminum compounds such as antimony alkoxide compounds, germanium alkoxide compounds, indium alkoxide compounds, indium chelate compounds, manganese alkoxide compounds, manganese chelate compounds, tin alkoxide compounds, tin chelate compounds, aluminum silicon alkoxide compounds, aluminum titanium alkoxide compounds, And aluminum zirconium alkoxide compounds. .

  As the organometallic compound, an organic zirconium compound, an organic titanyl compound, and an organoaluminum compound are particularly preferably used because of low residual potential and good electrophotographic characteristics.

  As the binder resin, polyvinyl alcohol, polyvinyl methyl ether, poly-N-vinylimidazole, polyethylene oxide, ethyl cellulose, methyl cellulose, ethylene-acrylic acid copolymer, polyamide, polyimide, casein, gelatin, polyethylene, polyester, phenol resin, Examples include known vinyl chloride-vinyl acetate copolymers, epoxy resins, polyvinyl pyrrolidone, polyvinyl pyridine, polyurethane, polyglutamic acid, polyacrylic acid, and the like. When these are used in combination of two or more, the mixing ratio can be appropriately set as necessary.

  The undercoat layer 4 includes vinyltrichlorosilane, vinyltrimethoxysilane, vinyltriethoxysilane, vinyltris-2-methoxyethoxysilane, vinyltriacetoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-methacryloxypropyltri Methoxysilane, γ-aminopropyltriethoxysilane, γ-chloropropyltrimethoxysilane, γ-2-aminoethylaminopropyltrimethoxysilane, γ-mercapropropyltrimethoxysilane, γ-ureidopropyltriethoxysilane, β- A silane coupling agent such as 3,4-epoxycyclohexyltrimethoxysilane may be contained.

  In the undercoat layer 4, an electron transporting pigment can also be mixed / dispersed from the viewpoints of lowering the residual potential and environmental stability. Examples of the electron transport pigment include organic pigments such as perylene pigments, bisbenzimidazole perylene pigments, polycyclic quinone pigments, indigo pigments, quinacridone pigments described in JP-A-47-30330, cyano groups, nitro groups, Examples thereof include organic pigments such as bisazo pigments and phthalocyanine pigments having electron-withdrawing substituents such as nitroso groups and halogen atoms, and inorganic pigments such as zinc oxide and titanium oxide.

  Among these pigments, perylene pigments, bisbenzimidazole perylene pigments, polycyclic quinone pigments, zinc oxide or titanium oxide are preferably used because of their high electron mobility.

  In addition, the surface of these pigments may be surface-treated with the above coupling agent or binder resin for the purpose of controlling dispersibility and charge transporting property.

  If the amount of the electron transporting pigment is too large, the strength of the undercoat layer 4 is lowered and causes a coating film defect. % Used.

  In addition, it is preferable to add various kinds of fine powders of organic compounds or fine powders of inorganic compounds to the undercoat layer 4 for the purpose of improving electrical characteristics and light scattering properties. In particular, white pigments such as titanium oxide, zinc oxide, zinc white, zinc sulfide, lead white, lithopone, inorganic pigments such as alumina, calcium carbonate, barium sulfate, and the like, polytetrafluoroethylene resin particles, benzoguanamine resin particles, Styrene resin particles and the like are effective.

  The added fine powder preferably has a particle size of 0.01 to 2 μm. The fine powder is added as necessary, but the addition amount is preferably 10 to 90 mass%, more preferably 30 to 80 mass%, based on the total solid content of the undercoat layer 4. .

  The undercoat layer 4 is formed using an undercoat layer forming coating solution containing the above-described constituent materials. The organic solvent used in the coating solution for forming the undercoat layer is one that dissolves an organometallic compound or a binder resin and does not cause gelation or aggregation when an electron transporting pigment is mixed and / or dispersed. If it is.

  Examples of the organic solvent include methanol, ethanol, n-propanol, n-butanol, benzyl alcohol, methyl cellosolve, ethyl cellosolve, acetone, methyl ethyl ketone, cyclohexanone, methyl acetate, n-butyl acetate, dioxane, tetrahydrofuran, and methylene chloride. , Chloroform, chlorobenzene, toluene and the like. These can be used individually by 1 type or in mixture of 2 or more types.

  As a method for mixing and / or dispersing each constituent material, a conventional method using a ball mill, a roll mill, a sand mill, an attritor, a vibrating ball mill, a colloid mill, a paint shaker ultrasonic wave, or the like is applied. Mixing and / or dispersion is performed in an organic solvent.

  As a coating method for forming the undercoat layer 4, a normal method such as a blade coating method, a wire bar coating method, a spray coating method, a dip coating method, a bead coating method, an air knife coating method, or a curtain coating method is used. be able to.

  The drying is usually performed at a temperature at which the solvent can be evaporated and a film can be formed. In particular, the conductive support 2 subjected to the acidic solution treatment and the boehmite treatment is preferably formed with the undercoat layer 4 because the defect concealing power of the substrate tends to be insufficient.

  The thickness of the undercoat layer 4 is preferably 0.01 to 30 μm, more preferably 0.05 to 30 μm, still more preferably 0.1 to 30 μm, and particularly preferably 0.2 to 25 μm.

  The charge generation layer 5 includes a charge generation material and, if necessary, a binder resin.

  Known charge generation materials include azo pigments such as bisazo and trisazo, condensed aromatic pigments such as dibromoanthanthrone, organic pigments such as perylene pigments, pyrrolopyrrole pigments, and phthalocyanine pigments, and inorganic pigments such as trigonal selenium and zinc oxide. Can be used. As the charge generation material, metal and metal-free phthalocyanine pigments, trigonal selenium, dibromoanthanthrone and the like are particularly preferable when a light source having an exposure wavelength of 380 to 500 nm is used. Among them, hydroxygallium phthalocyanine disclosed in JP-A-5-263007 and JP-A-5-279591, chlorogallium phthalocyanine disclosed in JP-A-5-98181, JP-A-5-140472 and special Dichlorotin phthalocyanine disclosed in Kaihei 5-140473 and titanyl phthalocyanine disclosed in JP-A-4-189873 and JP-A-5-43813 are particularly preferred.

  The binder resin can be selected from a wide range of insulating resins. It can also be selected from organic photoconductive polymers such as poly-N-vinyl carbazole, polyvinyl anthracene, polyvinyl pyrene and polysilane.

  The binder resin is preferably polyvinyl butyral resin, polyarylate resin (polycondensate of bisphenol A and phthalic acid, etc.), polycarbonate resin, polyester resin, phenoxy resin, vinyl chloride-vinyl acetate copolymer, polyamide resin, Insulating resins such as acrylic resin, polyacrylamide resin, polyvinyl pyridine resin, cellulose resin, urethane resin, epoxy resin, casein, polyvinyl alcohol resin, and polyvinyl pyrrolidone resin can be mentioned, but are not limited thereto. These binder resins can be used individually by 1 type or in mixture of 2 or more types.

  The charge generation layer 5 is formed by vapor deposition of a charge generation material or a coating solution for forming a charge generation layer containing a charge generation material and a binder resin. When the charge generation layer 5 is formed using a charge generation layer forming coating solution, the blending ratio (mass ratio) of the charge generation material and the binder resin is preferably in the range of 10: 1 to 1:10.

  As a method for dispersing each of the constituent materials in the charge generation layer forming coating solution, a usual method such as a ball mill dispersion method, an attritor dispersion method, a sand mill dispersion method, or the like can be used. At this time, a condition that the crystal form of the pigment is not changed by the dispersion is required. Further, at the time of this dispersion, it is effective that the particles have a particle size of preferably 0.5 μm or less, more preferably 0.3 μm or less, and further preferably 0.15 μm or less.

  Solvents used for dispersion include methanol, ethanol, n-propanol, n-butanol, benzyl alcohol, methyl cellosolve, ethyl cellosolve, acetone, methyl ethyl ketone, cyclohexanone, methyl acetate, n-butyl acetate, dioxane, tetrahydrofuran, and methylene chloride. Ordinary organic solvents such as chloroform, chlorobenzene and toluene. These can be used individually by 1 type or in mixture of 2 or more types.

  When forming the charge generation layer 5 using the coating solution for forming the charge generation layer, the coating methods are blade coating method, wire bar coating method, spray coating method, dip coating method, bead coating method, air knife coating. Ordinary methods such as a method and a curtain coating method can be used.

  The film thickness of the charge generation layer 5 is preferably 0.1 to 5 μm, more preferably 0.2 to 2.0 μm.

  The charge transport layer 6 includes a charge transport material and a binder resin, or a polymer charge transport material.

  Charge transport materials include quinone compounds such as p-benzoquinone, chloranil, bromanyl, anthraquinone, tetracyanoquinodimethane compounds, fluorenone compounds such as 2,4,7-trinitrofluorenone, xanthone compounds, benzophenone compounds , Electron transport compounds such as cyanovinyl compounds and ethylene compounds, triarylamine compounds, benzidine compounds, arylalkane compounds, aryl-substituted ethylene compounds, stilbene compounds, anthracene compounds, hydrazone compounds, etc. Examples thereof include, but are not limited to, hole transporting compounds. These charge transport materials can be used singly or in combination of two or more.

  Moreover, as a charge transport material, the compound shown by the following general formula (V-1), (V-2), or (V-3) from a mobility viewpoint is preferable.

ここで、上記式（Ｖ−１）中、Ｒ^１４は、水素原子又はメチル基を、ｋは１又は２を、Ａｒ^６及びＡｒ^７はそれぞれ独立に置換又は未置換のアリール基、−Ｃ_６Ｈ_４−Ｃ（Ｒ^１８）＝Ｃ（Ｒ^１９）（Ｒ^２０）、又は−Ｃ_６Ｈ_４−ＣＨ＝ＣＨ−ＣＨ＝Ｃ（Ａｒ）_２を表し、置換基としてはハロゲン原子、炭素数１〜５のアルキル基、炭素数１〜５のアルコキシ基、又は炭素数１〜３のアルキル基で置換された置換アミノ基を示す。また、Ｒ^１８、Ｒ^１９及びＲ^２０はそれぞれ独立に水素原子、置換若しくは未置換のアルキル基、又は置換若しくは未置換のアリール基を、Ａｒは置換又は未置換のアリール基を示す。

Here, in the formula (V-1), R ¹⁴ is a hydrogen atom or a methyl group, k is 1 or 2, Ar ⁶ and Ar ⁷ are each independently a substituted or unsubstituted aryl group, —C _6. H ₄ —C (R ¹⁸ ) ═C (R ¹⁹ ) (R ²⁰ ), or —C ₆ H ₄ —CH═CH—CH═C (Ar) ₂ is represented, and the substituent is a halogen atom, carbon number 1 The substituted amino group substituted by the alkyl group of -5, a C1-C5 alkoxy group, or a C1-C3 alkyl group is shown. R ¹⁸ , R ¹⁹ and R ²⁰ each independently represent a hydrogen atom, a substituted or unsubstituted alkyl group, or a substituted or unsubstituted aryl group, and Ar represents a substituted or unsubstituted aryl group.

ここで、上記式（Ｖ−２）中、Ｒ^１５及びＲ^１５’はそれぞれ独立に水素原子、ハロゲン原子、炭素数１〜５のアルキル基又は炭素数１〜５のアルコキシ基を、Ｒ^１６、Ｒ^１６’、Ｒ^１７及びＲ^１７’はそれぞれ独立に、ハロゲン原子、炭素数１〜５のアルキル基、炭素数１〜５のアルコキシ基、炭素数１〜２のアルキル基で置換されたアミノ基、置換若しくは未置換のアリール基、−Ｃ_６Ｈ_４−Ｃ（Ｒ^１８）＝Ｃ（Ｒ^１９）（Ｒ^２０）、又は、−Ｃ_６Ｈ_４−ＣＨ＝ＣＨ−ＣＨ＝Ｃ（Ａｒ）_２を、Ｒ^１８、Ｒ^１９及びＲ^２０はそれぞれ独立に水素原子、置換若しくは未置換のアルキル基、又は置換若しくは未置換のアリール基を、Ａｒは置換又は未置換のアリール基を示す。ｍ及びｎはそれぞれ独立に０〜２の整数を示す。

Here, in the above formula (V-2), R ¹⁵ and R ¹⁵ ′ each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 5 carbon atoms, or an alkoxy group having 1 to 5 carbon atoms, R ¹⁶ , R ¹⁶ ′, R ^17, and R ¹⁷ ′ are each independently an amino group substituted with a halogen atom, an alkyl group having 1 to 5 carbon atoms, an alkoxy group having 1 to 5 carbon atoms, or an alkyl group having 1 to 2 carbon atoms. , A substituted or unsubstituted aryl group, —C ₆ H ₄ —C (R ¹⁸ ) ═C (R ¹⁹ ) (R ²⁰ ), or —C ₆ H ₄ —CH═CH—CH═C (Ar) ₂ R ¹⁸ , R ¹⁹ and R ²⁰ each independently represents a hydrogen atom, a substituted or unsubstituted alkyl group, or a substituted or unsubstituted aryl group, and Ar represents a substituted or unsubstituted aryl group. m and n each independently represents an integer of 0 to 2.

ここで、上記式（Ｖ−３）中、Ｒ^２１は水素原子、炭素数１〜５のアルキル基、炭素数１〜５のアルコキシ基、置換若しくは未置換のアリール基、又は、−ＣＨ＝ＣＨ−ＣＨ＝Ｃ（Ａｒ）_２を示す。Ａｒは、置換又は未置換のアリール基を示す。Ｒ^２２、Ｒ^２２’、Ｒ^２３’、及びＲ^２３はそれぞれ独立に、水素原子、ハロゲン原子、炭素数１〜５のアルキル基、炭素数１〜５のアルコキシ基、炭素数１〜２のアルキル基で置換されたアミノ基、又は置換若しくは未置換のアリール基を示す。

Here, in the formula (V-3), R ²¹ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, an alkoxy group having 1 to 5 carbon atoms, a substituted or unsubstituted aryl group, or —CH═CH. -CH = C (Ar) ₂ is shown. Ar represents a substituted or unsubstituted aryl group. R ²² , R ²² ′, R ²³ ′ and R ²³ are each independently a hydrogen atom, a halogen atom, an alkyl group having 1 to 5 carbon atoms, an alkoxy group having 1 to 5 carbon atoms, or an alkyl having 1 to 2 carbon atoms. An amino group substituted with a group, or a substituted or unsubstituted aryl group is shown.

  Examples of the binder resin used for the charge transport layer 6 include polycarbonate resin, polyester resin, methacrylic resin, acrylic resin, polyvinyl chloride resin, polyvinylidene chloride resin, polystyrene resin, polyvinyl acetate resin, styrene-butadiene copolymer, and vinylidene chloride. -Acrylonitrile copolymer, vinyl chloride-vinyl acetate copolymer, vinyl chloride-vinyl acetate-maleic anhydride copolymer, silicone resin, silicone-alkyd resin, phenol-formaldehyde resin, styrene-alkyd resin, and the like. These binder resins can be used individually by 1 type or in mixture of 2 or more types. The blending ratio (mass ratio) of the charge transport material and the binder resin is preferably 10: 1 to 1: 5.

  As the polymer charge transport material, known materials having charge transport properties such as poly-N-vinylcarbazole and polysilane can be used. In particular, the polyester polymer charge transport materials disclosed in JP-A-8-176293 and JP-A-8-208820 have a high charge transporting property and are particularly preferable.

  Although the polymer charge transport material alone can be used as a constituent material of the charge transport layer 6, it may be mixed with the binder resin to form a film.

  The charge transport layer 6 is formed using a charge transport layer forming coating solution containing the above-described constituent materials.

  Examples of the solvent for the coating solution for forming the charge transport layer include aromatic hydrocarbons such as benzene, toluene, xylene and chlorobenzene, ketones such as acetone and 2-butanone, and halogenated fats such as methylene chloride, chloroform and ethylene chloride. Examples thereof include ordinary organic solvents such as aromatic hydrocarbons, cyclic ethers such as tetrahydrofuran and ethyl ether, and linear ethers. These can be used individually by 1 type or in mixture of 2 or more types.

  As a coating method of the coating solution for forming the charge transport layer, a normal method such as a blade coating method, a wire bar coating method, a spray coating method, a dip coating method, a bead coating method, an air knife coating method, or a curtain coating method should be used. Can do.

  The film thickness of the charge transport layer 6 is preferably 5 to 50 μm, more preferably 10 to 30 μm.

  In the photosensitive layer 3, additives such as an antioxidant, a light stabilizer, and a heat stabilizer are added for the purpose of preventing deterioration of the photoreceptor due to ozone, an oxidizing gas, or light or heat generated in the image forming apparatus. Can be added.

  Examples of the antioxidant include hindered phenol, hindered amine, paraphenylenediamine, arylalkane, hydroquinone, spirochroman, spiroidanone and derivatives thereof, organic sulfur compounds, and organic phosphorus compounds. Examples of the light stabilizer include derivatives such as benzophenone, benzotriazole, dithiocarbamate, and tetramethylpiperidine.

  The photosensitive layer 3 can contain at least one electron accepting substance for the purpose of improving sensitivity, reducing residual potential, reducing fatigue during repeated use, and the like.

Examples of the electron acceptor include succinic anhydride, maleic anhydride, dibromomaleic anhydride, phthalic anhydride, tetrabromophthalic anhydride, tetracyanoethylene, tetracyanoquinodimethane, o-dinitrobenzene, m-dinitrobenzene, Examples include chloranil, dinitroanthraquinone, trinitrofluorenone, picric acid, o-nitrobenzoic acid, p-nitrobenzoic acid, and phthalic acid. Of these, fluorenone-based, quinone-based, and benzene derivatives having electron-withdrawing substituents such as Cl, CN, NO ₂ are particularly preferable.

  In the electrophotographic photosensitive member of this embodiment, the protective layer 7 is an outermost surface layer containing a resin having a crosslinked structure. Further, the resin needs to be an oxetane resin containing an oxetane compound as a resin component.

  As said oxetane compound, the compound shown by the following general formula (VI) and the following general formula (VII) can be mentioned, for example.

ここで、式（ＶＩ）中、Ｒ^３１は、水素原子、メチル基、エチル基、プロピル基若しくはブチル基等の炭素数１〜６のアルキル基、炭素数１〜６のフルオロアルキル基、アリル基、アリール基、フリル基又はチエニル基を示し、Ｒ^３２は、メチル基、エチル基、プロピル基若しくはブチル基等の炭素数１〜６のアルキル基、１−プロペニル基、２−プロペニル基、２−メチル−１−プロペニル基、２−メチル−２−プロペニル基、１−ブテニル基、２−ブテニル基或いは３?ブテニル基等の炭素数２〜６のアルケニル基、フェニル基、ベンジル基、フルオロベンジル基、メトキシベンジル基若しくはフェノキシエチル基等の芳香環を有する基、エチルカルボニル基、プロピルカルボニル基若しくはブチルカルボニル基等の炭素数２〜６のアルキルカルボニル基、エトキシカルボニル基、プロポキシカルボニル基若しくはブトキシカルボニル基等の炭素数２〜６のアルコキシカルボニル基、トリメトキシシリル基、メチルジメトキシシリル基、トリエトキシシリル基、エチルジエトキシシリル基、トリメトキシシリルメチル基及びトリエトキシシリルプロピル基などのアルコキシルシリルを有する基、又は、エチルカルバモイル基、プロピルカルバモイル基、ブチルカルバモイル基若しくはペンチルカルバモイル基等の炭素数２〜６のＮ−アルキルカルバモイル基等を示す。

Here, in the formula (VI), R ³¹ is a hydrogen atom, a methyl group, an ethyl group, a propyl group or a butyl group, such as an alkyl group having 1 to 6 carbon atoms, a fluoroalkyl group having 1 to 6 carbon atoms, or an allyl group. R ³² represents an alkyl group having 1 to 6 carbon atoms such as a methyl group, an ethyl group, a propyl group or a butyl group, a 1-propenyl group, a 2-propenyl group, 2- C2-C6 alkenyl group such as methyl-1-propenyl group, 2-methyl-2-propenyl group, 1-butenyl group, 2-butenyl group or 3-butenyl group, phenyl group, benzyl group, fluorobenzyl group A group having an aromatic ring such as methoxybenzyl group or phenoxyethyl group, an alkyl group having 2 to 6 carbon atoms such as ethylcarbonyl group, propylcarbonyl group or butylcarbonyl group; C2-C6 alkoxycarbonyl group such as rucarbonyl group, ethoxycarbonyl group, propoxycarbonyl group or butoxycarbonyl group, trimethoxysilyl group, methyldimethoxysilyl group, triethoxysilyl group, ethyldiethoxysilyl group, trimethoxy A group having an alkoxylsilyl group such as a silylmethyl group and a triethoxysilylpropyl group, or an N-alkylcarbamoyl group having 2 to 6 carbon atoms such as an ethylcarbamoyl group, a propylcarbamoyl group, a butylcarbamoyl group or a pentylcarbamoyl group .

ここで、式（ＶＩＩ）中、Ｒ^３３は、水素原子、メチル基、エチル基、プロピル基若しくはブチル基等の炭素数１〜６のアルキル基、炭素数１〜６のフルオロアルキル基、アリル基、アリール基、フリル基又はチエニル基を示し、ｋ１は０又は１以上の整数を示し、Ｒ^３４は、エチレン基、プロピレン基若しくはブチレン基等の直鎖状若しくは分枝状アルキレン基、ポリ（エチレンオキシ）基若しくはポリ（プロピレンオキシ）基等の直鎖状若しくは分枝状ポリ（アルキレンオキシ）基、プロペニレン基、メチルプロペニレン基若しくはブテニレン基等の直鎖状若しくは分枝状不飽和炭化水素基、カルボニル基、カルボニル基を含むアルキレン基、カルボキシル基を含むアルキレン基、カルバモイル基を含むアルキレン基、下記一般式（ＶＩＩＩ）で示される２価の基、下記一般式（ＩＸ）で示される２価の基、又は、下記一般式（Ｘ）で示される２価の基を示す。

Here, in the formula (VII), R ³³ represents a hydrogen atom, a methyl group, an ethyl group, a propyl group or a butyl group, such as an alkyl group having 1 to 6 carbon atoms, a fluoroalkyl group having 1 to 6 carbon atoms, or an allyl group. , Aryl group, furyl group or thienyl group, k1 represents 0 or an integer of 1 or more, R ³⁴ represents a linear or branched alkylene group such as ethylene group, propylene group or butylene group, poly (ethylene Linear or branched unsaturated hydrocarbon groups such as linear or branched poly (alkyleneoxy) groups such as oxy) or poly (propyleneoxy) groups, propenylene groups, methylpropenylene groups or butenylene groups , A carbonyl group, an alkylene group containing a carbonyl group, an alkylene group containing a carboxyl group, an alkylene group containing a carbamoyl group, the following general formula (V Divalent groups represented by II), the divalent group represented by the following general formula (IX), or a divalent group represented by the following general formula (X).

ここで、式（ＶＩＩＩ）中、Ｒ^３５は、水素原子、メチル基、エチル基、プロピル基若しくはブチル基等の炭素数１〜４のアルキル基、メトキシ基、エトキシ基、プロポキシ基若しくはブトキシ基等の炭素数１〜４のアルコキシ基、塩素原子若しくは臭素原子等のハロゲン原子、ニトロ基、シアノ基、メルカプト基、低級アルキルカルボキシル基、カルボキシル基、又はカルバモイル基を示す。また、式（ＩＸ）中、Ｒ^３６は、酸素原子、硫黄原子、メチレン基、ＮＨ、ＳＯ、ＳＯ_２、Ｃ（ＣＦ_３）_２、又はＣ（ＣＨ_３）_２を示す。また、式（Ｘ）中、Ｒ^３７、Ｒ^３８及びＲ^３９はそれぞれ独立に、メチル基、エチル基、プロピル基若しくはブチル基等の炭素数１〜４のアルキル基、又はアリール基を示し、ｋ２は、０〜２０００の整数を示す。

Here, in the formula (VIII), R ³⁵ represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms such as a methyl group, an ethyl group, a propyl group or a butyl group, a methoxy group, an ethoxy group, a propoxy group or a butoxy group. An alkoxy group having 1 to 4 carbon atoms, a halogen atom such as a chlorine atom or a bromine atom, a nitro group, a cyano group, a mercapto group, a lower alkyl carboxyl group, a carboxyl group, or a carbamoyl group. In the formula (IX), R ³⁶ represents an oxygen atom, a sulfur atom, a methylene group, NH, SO, SO ₂ , C (CF ₃ ) ₂ , or C (CH ₃ ) ₂ . In the formula (X), R ³⁷ , R ³⁸ and R ³⁹ each independently represents an alkyl group having 1 to 4 carbon atoms such as a methyl group, an ethyl group, a propyl group or a butyl group, or an aryl group; Represents an integer of 0 to 2000.

  Preferable examples of the oxetane compound represented by the general formula (VI) include oxetane compounds represented by the following formulas (VI-1) to (VI-13).

  Preferable examples of the oxetane compound represented by the general formula (VII) include oxetane compounds represented by the following formulas (VII-1) to (VII-3).

  The oxetane compound described above can be synthesized by a known method. For example, the hydroxyl group of a 1,3-diol derivative is halogenated with hydrogen chloride or the like, and a tosyl group is introduced with p-toluenesulfonic acid chloride and the like, followed by elimination and cyclization with an alkali such as sodium hydroxide or potassium hydroxide. Or a method in which a 1,3-diol derivative is reacted with an alkyl carbonate compound such as diphenyl carbonate or diethyl carbonate under alkaline conditions, followed by decarboxylation and cyclization. is there. Further, when obtaining a bisoxetane compound, it can be synthesized by etherifying a compound having a hydroxyl group and a halide under alkaline conditions.

  The oxetane resin preferably further contains an epoxy compound having an epoxy group as a resin component. Thereby, it becomes possible to further improve the durability of the protective layer.

  Examples of the epoxy compound include phenyl glycidyl ether and butyl glycidyl ether as epoxy compounds having one epoxy group, and hexanediol diglycidyl ether and tetraethylene glycol diester as epoxy compounds having two or more epoxy groups. Examples thereof include glycidyl ether, trimethylolpropane triglycidyl ether, bisphenol A diglycidyl ether, and a novolac type epoxy compound. In this case, the mixing ratio of the compound having an epoxy group is preferably 5 to 95 parts by weight with respect to 100 parts by weight of the total amount of the compound having an oxetane ring and the compound having an epoxy group.

  The content of the epoxy compound is preferably 0.1 to 20% by mass and more preferably 0.1 to 10% by mass with respect to the total amount of the oxetane compound and the epoxy compound. When the content is less than 0.1% by mass, the effect of improving the durability of the protective layer tends to be difficult to be obtained. On the other hand, when the content exceeds 20% by mass, the electrical characteristics are adversely affected. There is a tendency that the light transmittance becomes poor, a uniform cured film is not formed, or the smoothness of the surface of the protective layer is lost.

  The oxetane resin preferably further contains a phenol derivative having a methylol group as a resin component. Thereby, the cleaning property of the protective layer is improved and the effect of suppressing the deterioration of the protective layer due to the discharge product is improved, which is advantageous in maintaining high image quality. Such an effect is considered to be due to the combination of an oxetane compound and a phenol derivative having a methylol group, thereby improving the antioxidant ability and improving the wear resistance.

Examples of the phenol derivative having a methylol group include monomers of monomethylolphenols, dimethylolphenols or trimethylolphenols, mixtures thereof, oligomers thereof, or mixtures of these monomers and oligomers. Such phenol derivatives having a methylol group include resorcin, bisphenol, etc., substituted phenols containing one hydroxyl group such as phenol, cresol, xylenol, paraalkylphenol, paraphenylphenol, and two hydroxyl groups such as catechol, resorcinol, hydroquinone, etc. It is obtained by reacting a compound having a phenol structure, such as bisphenols such as substituted phenols, bisphenol A and bisphenol Z, biphenols, etc., with formaldehyde, paraformaldehyde, etc. in the presence of an acid catalyst or an alkali catalyst, Generally what is marketed as a phenol resin can also be used. In the present specification, a relatively large molecule having about 2 to 20 repeating molecular structural units is referred to as an oligomer, and a molecule smaller than that is referred to as a monomer. As the acid catalyst, sulfuric acid, paratoluenesulfonic acid, phosphoric acid and the like are used. Further, as the alkali catalyst, hydroxides or amine catalysts of alkali metals and alkaline earth metals such as NaOH, KOH, Ca (OH) ₂ and Ba (OH) ₂ are used. Examples of the amine catalyst include, but are not limited to, ammonia, hexamethylenetetramine, trimethylamine, triethylamine, and triethanolamine. When a basic catalyst is used, the carrier is remarkably trapped by the remaining catalyst, and the electrophotographic characteristics tend to be deteriorated. Therefore, it is preferable to inactivate or remove by neutralizing with an acid or contacting with an adsorbent such as silica gel or an ion exchange resin.

  Of the phenol derivatives having a methylol group, a phenol resin is preferable, and a resol type phenol resin is more preferable. The molecular weight of the phenol derivative having a methylol group is not particularly limited, but from the viewpoint of solubility and coating properties, the molecular weight is preferably not less than the molecular weight of the resol monomer and not more than 10,000.

  The content of the phenol derivative having a methylol group is preferably 10 to 90% by mass, more preferably 30 to 60% by mass, based on the total amount of the oxetane compound and the phenol derivative having a methylol group. preferable. When the content is less than 10% by mass, the effect of improving the cleaning property of the protective layer and the effect of suppressing the deterioration of the protective layer due to the discharge product tend to be difficult to be obtained. If it exceeds, electrical characteristics such as residual potential tend to deteriorate.

The protective layer, which is a layer containing an oxetane resin, is a charge transport material having at least one functional group selected from a hydroxyl group, a carboxyl group, an alkoxysilyl group, an epoxy group, an oxetane group, a thiol group, and an amino group. further including. Note that these charge transport materials may be incorporated into the resin by reacting with the oxetane compound or the oxetane resin.

  Examples of the charge transport material having at least one functional group selected from a hydroxyl group, a carboxyl group, an alkoxysilyl group, an epoxy group, an oxetane group, a thiol group, and an amino group include the following general formulas (I), (II), or It is preferably at least one selected from compounds represented by (III).

F-[(X ¹ ) _m ^1- (R ¹ ) _{m 2} -Y] _{m 3} (I)
Here, in formula (I), F represents an organic group derived from a compound having a hole transporting ability, X ¹ represents an oxygen atom or a sulfur atom, R ¹ represents an alkylene group, Y represents a hydroxyl group, a carboxyl group, A thiol group or an amino group, m1 and m2 each independently represent 0 or 1, and m3 represents an integer of 1 to 4;

^{_{F - [(X 2) n1}} - (R 2) n2 - (Z) n3 G] n4 (II)
Here, in formula (II), F is an organic group derived from a compound having a hole transport ability, X ² is an oxygen atom or a sulfur atom, R ² is an alkylene group, Z is an oxygen atom, a sulfur atom , NH or COO, G represents an epoxy group or oxetane group, n1, n2 and n3 each independently represents 0 or 1, and n4 represents an integer of 1 to 4.

F- [D-Si (R ³ ) _(3-a) Q _a ] _b (III)
Here, in Formula (III), F is an organic group derived from a compound having a hole transporting ability, D is a divalent group having flexibility, R ³ is a hydrogen atom, substituted or unsubstituted An alkyl group or a substituted or unsubstituted aryl group, Q represents a hydrolyzable group, a represents an integer of 1 to 3, and b represents an integer of 1 to 4.

In addition, as the divalent group D having flexibility, specifically, a site of F for imparting photoelectric characteristics, a substituted silicon group contributing to the construction of a three-dimensional inorganic glassy network, It is a divalent group that plays a role in linking. In addition, D represents an organic group structure that imparts moderate flexibility to the portion of the inorganic glassy network that is hard but brittle, and plays a role of improving mechanical toughness as a film. Specific examples _{D, -C α H 2α -,} - C β H 2β-2 -, - C γ H 2γ-4 - 2 divalent hydrocarbon group (here represented by, alpha is 1 to 15 Represents an integer, β represents an integer of 2 to 15, and γ represents an integer of 3 to 15), —COO—, —S—, —O—, —CH ₂ —C ₆ H ₄ —, —N═. CH—, — (C ₆ H ₄ ) — (C ₆ H ₄ ) —, and a characteristic group having a structure in which these characteristic groups are arbitrarily combined, and further, the constituent atoms of these characteristic groups are substituted with other substituents. And the like. The hydrolyzable group Q is preferably an alkoxy group, more preferably an alkoxy group having 1 to 15 carbon atoms.

  As the organic group F derived from the compound having a hole transporting ability in the compound represented by the general formula (I), (II) or (III), a compound represented by the following general formula (XI) is preferable.

ここで、上記式（ＸＩ）中、Ａｒ^１、Ａｒ^２、Ａｒ^３及びＡｒ^４はそれぞれ独立に置換又は未置換のアリール基を示し、Ａｒ^５は置換若しくは未置換のアリール基又はアリーレン基を示し、且つＡｒ^１〜Ａｒ^５のうち１〜４個は、上記式（Ｉ）、（ＩＩ）、又は（ＩＩＩ）で示される化合物における−［（Ｘ^１）_ｍ１−（Ｒ^１）_ｍ２−Ｙ］、−［（Ｘ^２）_ｎ１−（Ｒ^２）_ｎ２−（Ｚ）_ｎ３Ｇ］、又は−［Ｄ−Ｓｉ（Ｒ^３）_{（３−ａ）}Ｑ_ａ］で示される部位と結合手を有する。

Here, in the formula (XI), Ar ¹ , Ar ² , Ar ³ and Ar ⁴ each independently represent a substituted or unsubstituted aryl group, and Ar ⁵ represents a substituted or unsubstituted aryl group or arylene group. And ^{1 to} 4 of Ar ^{1 to} Ar ⁵ are-[(X ¹ ) _m1- (R ¹ ) _m2 -Y] in the compound represented by the formula (I), (II), or (III). _{^{, - [(X 2) n1}} - (R 2) n2 - (Z) n3 G], or - has a portion with a bond represented by _{^{[D-Si (R 3)}} (3-a) Q a].

Specific examples of the substituted or unsubstituted aryl group represented by Ar ^{1 to} Ar ⁴ in the compound represented by the general formula (XI) include aryl represented by the following formulas (XI-1) to (XI-7). Groups are preferred.

  As Ar in the aryl group represented by the formula (XI-7), an aryl group represented by the following formula (XI-8) or (XI-9) is preferable.

  Moreover, as Z in the aryl group represented by the above formula (XI-7), divalent groups represented by the following formulas (XI-10) to (XI-17) are preferable.

Here, in the above formula (XI-1) ~ (XI -17), R 6 is a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, an alkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms A substituted or unsubstituted phenyl group, or an aralkyl group having 7 to 10 carbon atoms, R ^{7 to} R ¹³ are each independently a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, or 1 carbon atom. An alkoxy group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a phenyl group substituted or unsubstituted with them, an aralkyl group having 7 to 10 carbon atoms, or a halogen atom, m and s are each independently 0; Or 1, q and r each independently represent an integer of 1 to 10, and t each independently represents an integer of 1 to 3.

In the formulas (XI-1) to (XI-7), X represents-[(X ¹ ) _m1- (R ¹ ) in the compound represented by the formula (I), (II), or (III). _{^{m2 -Y], - [(X}} 2) n1 - (R 2) n2 - (Z) n3 G], or _{^{- [D-Si (R 3}} ) (3-a) bind to sites represented by _{Q a]} Have a hand.

  In the formulas (XI-16) to (XI-17), W represents a divalent group represented by the following formulas (XI-18) to (XI-26). In formula (XI-25), u represents an integer of 0 to 3.

In addition, the specific structure of Ar ⁵ in the general formula (XI) is as follows. When k = 0, the structure of m = 1 in the specific structure of Ar ^{1 to} Ar ⁴ and when Ar = 1, the Ar 5 ^The structure of m = 0 in the specific structure of ^{1 to} Ar ⁴ is given.

  Specific examples of the compound represented by the general formula (I) include the following compounds (I-1) to (I-36). In the following table, Me or a bond is described but a substituent is not described, a methyl group, Et represents an ethyl group.

  Specific examples of the compound represented by the general formula (II) include the following compounds (II-1) to (II-61). In the following table, Me or a bond is described but a substituent is not described, a methyl group, Et represents an ethyl group.

  As the compound represented by the above general formula (I) and the compound represented by the above general formula (II), those synthesized by a known synthesis method can be used. The compounds represented by the general formulas (II-48) to (II-61) include, for example, an arylamine compound having a charge transporting structure and a halogen compound represented by the following general formula (OX-1): Or obtained by reacting an oxetane compound having a hydroxyl group represented by the following general formula (OX-2) with a charge transporting compound having a halogenated alkyl group Can be used. In addition, the halide represented by the following general formula (OX-1) can be synthesized, for example, by halogenating two hydroxyl groups of a trimethylol derivative and then cyclizing.

ここで、式（ＯＸ−１）中、Ｒ^５０は、水素又は炭素数１〜８の分岐があってもよいアルキル基を示し、式（ＯＸ−２）中、Ｒ^５１は、水素又は炭素数１〜８の分岐があってもよいアルキル基を示す。

Here, in Formula (OX-1), R ⁵⁰ represents hydrogen or an alkyl group that may have 1 to 8 carbon atoms, and in Formula (OX-2), R ⁵¹ represents hydrogen or carbon number. The alkyl group which may have 1-8 branches is shown.

Specific examples of the compound represented by the general formula (III) include the following compounds (III-1) to (III-61). In addition, the following compounds (III-1) to (III-61) combine Ar ^{1 to} Ar ⁵ and k of the compound represented by the general formula (XI) as shown in the following table, and an alkoxysilyl group (S) is the specific one shown in the table below.

  Further, conductive particles may be added to the protective layer 7 in order to reduce the residual potential. Examples of the conductive particles include metals, metal oxides, and carbon black. Among these, metals or metal oxides are more preferable. Examples of the metal include aluminum, zinc, copper, chromium, nickel, silver, and stainless steel, or those obtained by depositing these metals on the surface of plastic particles. Examples of the metal oxide include zinc oxide, titanium oxide, tin oxide, antimony oxide, indium oxide, bismuth oxide, tin-doped indium oxide, antimony and tantalum-doped tin oxide, and antimony-doped zirconium oxide. It is done. These can be used alone or in combination of two or more. When two or more types are used in combination, they may be simply mixed, or may be in the form of a solid solution or fusion. From the viewpoint of the transparency of the protective layer 7, the average particle diameter of the conductive particles is preferably 0.3 μm or less, and particularly preferably 0.1 μm or less.

In addition, a compound represented by the following general formula (XII-1) can also be added to the protective layer 7 in order to control various physical properties such as strength and film resistance of the protective layer 7.
Si (R ⁴⁰ ) _(4-c) Q _c (XII-1)
Here, in formula (XII-1), R ⁴⁰ represents a hydrogen atom, an alkyl group or a substituted or unsubstituted aryl group, Q represents a hydrolyzable group, and c represents an integer of 1 to 4.

  Specific examples of the compound represented by the general formula (XII-1) include the following silane coupling agents. Examples of silane coupling agents include tetrafunctional silanes such as tetramethoxysilane and tetraethoxysilane (c = 4); methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, methyltrimethoxyethoxysilane, vinyltri Methoxysilane, vinyltriethoxysilane, phenyltrimethoxysilane, γ-glycidoxypropylmethyldiethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-aminopropyltriethoxy Silane, γ-aminopropyltrimethoxysilane, γ-aminopropylmethyldimethoxysilane, N-β (aminoethyl) γ-aminopropyltriethoxysilane, (tridecafluoro-1,1,2,2-tetrahydrooctyl L) Triethoxysilane, (3,3,3-trifluoropropyl) trimethoxysilane, 3- (heptafluoroisopropoxy) propyltriethoxysilane, 1H, 1H, 2H, 2H-perfluoroalkyltriethoxysilane, 1H , 1H, 2H, 2H-perfluorodecyltriethoxysilane, trifunctional alkoxysilanes such as 1H, 1H, 2H, 2H-perfluorooctyltriethoxysilane (c = 3); dimethyldimethoxysilane, diphenyldimethoxysilane, methyl And bifunctional alkoxysilanes such as phenyldimethoxysilane (c = 2); monofunctional alkoxysilanes such as trimethylmethoxysilane (c = 1), and the like. Trifunctional and tetrafunctional alkoxysilanes are preferable for improving the strength of the film, and monofunctional and bifunctional alkoxysilanes are preferable for improving the flexibility and film formability.

  In addition, a silicon-based hard coat agent produced mainly from these coupling agents can also be used. Commercially available hard coat agents include KP-85, X-40-9740, X-40-2239 (manufactured by Shin-Etsu Silicone), and AY42-440, AY42-441, AY49-208 (manufactured by Toray Dow Corning). Etc.) can be used.

In addition, in order to increase the strength of the protective layer 7, it is also preferable to use a compound having two or more silicon atoms as shown in the general formula (XII-2).
B- (Si (R ⁴¹ ) _(3-d) Q _d ) ₂ (XII-2)
In the formula (VII-2), B represents a divalent organic group, R ⁴¹ represents a hydrogen atom, an alkyl group or a substituted or unsubstituted aryl group, Q represents a hydrolyzable group, a represents 1 to 1 An integer of 3 is shown.

  More specific examples of the compound represented by the general formula (XII-2) include the following compounds (XII-2-1) to (XII-2-16).

  Further, the protective layer 7 has a cyclic compound having a repeating structural unit represented by the following general formula (XII-3) in order to extend pot life, control film characteristics, reduce torque, and improve the uniformity of the coating film surface, Alternatively, a derivative from the compound can be contained.

ここで、式（ＸＩＩ−３）中、Ａ^１及びＡ^２は、それぞれ独立に一価の有機基を示す。

Here, in formula (XII-3), A ¹ and A ² each independently represent a monovalent organic group.

  Examples of the cyclic compound having the repeating structural unit represented by the general formula (XII-3) include commercially available cyclic siloxanes. Specifically, cyclic dimethylcyclosiloxanes such as hexamethylcyclotrisiloxane, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, dodecamethylcyclohexasiloxane, 1,3,5-trimethyl-1,3,5- Triphenylcyclotrisiloxane, 1,3,5,7-tetramethyl-1,3,5,7-tetraphenylcyclotetrasiloxane, 1,3,5,7,9-pentamethyl-1,3,5,7 , 9-pentaphenylcyclopentasiloxane and other cyclic methylphenylcyclosiloxanes, hexaphenylcyclotrisiloxane and other cyclic phenylcyclosiloxanes, and 3- (3,3,3-trifluoropropyl) methylcyclotrisiloxane and other fluorine Atom-containing cyclosiloxanes, methylhydrosiloxa Mixture, pentamethylcyclopentasiloxane, mention may be made of phenyl hydrosilyl group-containing cyclosiloxanes of hydrocyclosiloxane like, cyclic siloxanes and vinyl group-containing cyclosiloxanes such as penta vinyl pentamethylcyclopentasiloxane like. These cyclic siloxane compounds may be used alone or in combination of two or more.

  Furthermore, various fine particles can be added to control the antifouling substance adhesion, lubricity, hardness and the like on the surface of the electrophotographic photosensitive member. They can be used alone or in combination of two or more.

  Examples of the fine particles include silicon atom-containing fine particles. The silicon atom-containing fine particles are fine particles containing silicon as a constituent element, and specific examples include colloidal silica and silicone fine particles. The colloidal silica used as the silicon atom-containing fine particles preferably has an average particle diameter of 1 to 100 nm, more preferably 10 to 30 nm, in an acidic or alkaline aqueous dispersion, or an organic solvent such as alcohol, ketone or ester. What was chosen from what was disperse | distributed and generally marketed can be used. The solid content of colloidal silica in the protective layer 7 is not particularly limited, but preferably 0.1 to 0.1 based on the total solid content of the protective layer 7 in terms of film formability, electrical characteristics, and strength. It is used in the range of 50% by mass, more preferably in the range of 0.1-30% by mass.

  The silicone fine particles used as the silicon atom-containing fine particles are spherical and preferably have an average particle size of 1 to 500 nm, more preferably 10 to 100 nm, and are selected from silicone resin particles, silicone rubber particles, and silicone surface-treated silica particles. A commercially available product can be used.

  Silicone fine particles are small particles that are chemically inert and excellent in dispersibility in resin, and since the content required to obtain sufficient characteristics is low, the electron does not hinder the crosslinking reaction, The surface properties of the photographic photoreceptor can be improved. In other words, it is possible to improve the lubricity and water repellency of the surface of the electrophotographic photosensitive member while being uniformly incorporated into a strong cross-linked structure, and to maintain good wear resistance and adherence to contaminants over a long period of time. it can. The content of the silicone fine particles in the protective layer 7 is preferably in the range of 0.1 to 30% by mass, more preferably in the range of 0.5 to 10% by mass based on the total solid content of the protective layer 7. .

Other fine particles include fluorine-based fine particles such as ethylene tetrafluoride, trifluoride ethylene, propylene hexafluoride, vinyl fluoride, vinylidene fluoride, and the 8th Polymer Material Forum Lecture Proceedings p89. Fine particles made of a resin obtained by copolymerizing a fluororesin and a monomer having a hydroxyl group, ZnO—Al ₂ O ₃ , SnO ₂ —Sb ₂ O ₃ , In ₂ O ₃ —SnO ₂ , ZnO—TiO ₂ , MgO Examples thereof include semiconductive metal oxides such as —Al ₂ O ₃ , FeO—TiO ₂ , TiO ₂ , SnO ₂ , In ₂ O ₃ , ZnO, and MgO. For the same purpose, an oil such as silicone oil can be added.

  Examples of the silicone oil include silicone oils such as dimethylpolysiloxane, diphenylpolysiloxane, and phenylmethylsiloxane, amino-modified polysiloxane, epoxy-modified polysiloxane, carboxyl-modified polysiloxane, carbinol-modified polysiloxane, methacryl-modified polysiloxane, and mercapto. Examples include reactive silicone oils such as modified polysiloxanes and phenol-modified polysiloxanes. These may be added in advance to the protective layer-forming coating solution, or may be impregnated under reduced pressure or increased pressure after producing the photoreceptor.

  In addition, additives such as plasticizers, surface modifiers, antioxidants, and photodegradation inhibitors can also be used. Examples of the plasticizer include biphenyl, biphenyl chloride, terphenyl, dibutyl phthalate, diethylene glycol phthalate, dioctyl phthalate, triphenyl phosphate, methyl naphthalene, benzophenone, chlorinated paraffin, polypropylene, polystyrene, and various fluorohydrocarbons. An antioxidant having a hindered phenol, hindered amine, thioether, or phosphite partial structure can be added to the protective layer 7, which is effective in improving the potential stability and image quality when the environment changes.

  Examples of the antioxidant include the following compounds. For example, as the hindered phenol type, “Sumizer BHT-R”, “Sumizer MDP-S”, “Sumizer BBM-S”, “Sumizer WX-R”, “Sumizer NW”, “Sumizer BP-76”, “ Sumilizer BP-101 "," Sumilizer GA-80 "," Sumilizer GM "," Sumilizer GS "or more manufactured by Sumitomo Chemical Co., Ltd.," IRGANOX1010 "," IRGANOX1035 "," IRGANOX1076 "," IRGANOX1098 "," IRGANOX1098 "," IRGANOX1098 " ”,“ IRGANOX1222 ”,“ IRGANOX1330 ”,“ IRGANOX1425WL ”,“ IRGANOX1 20L "," IRGANOX 245 "," IRGANOX 259 "," IRGANOX 3114 "," IRGANOX 3790 "," IRGANOX 5057 "," IRGANOX 565 "or more, manufactured by Ciba Specialty Chemicals," ADK STAB AO-20 "," ADK STAB AO-30 "," ADEKA STAB " "AO-40", "ADK STAB AO-50", "ADK STAB AO-60", "ADK STAB AO-70", "ADK STAB AO-80", "ADK STAB AO-330" or more manufactured by Asahi Denka. Examples of hindered amines include “Sanol LS2626”, “Sanol LS765”, “Sanol LS770”, “Sanol LS744”, “Tinuvin 144”, “Tinuvin 622LD”, “Mark LA57”, “Mark LA67”, “Mark LA62”. ”,“ Mark LA68 ”,“ Mark LA63 ”,“ Smilizer TPS ”,“ Smilizer TP-D ”for thioethers,“ Mark 2112 ”,“ Mark PEP 8 ”,“ Mark PEP ”for phosphites -24G "," Mark PEP.36 "," Mark 329K "," Mark HP.10 ", and hindered phenols and hindered amine antioxidants are particularly preferable. Furthermore, these may be modified with a substituent such as an alkoxysilyl group capable of undergoing a crosslinking reaction with the material forming the crosslinked film.

  The protective layer 7 includes polyvinyl butyral resin, polyarylate resin (polycondensate of bisphenol A and phthalic acid, etc.), polycarbonate resin, polyester resin, phenoxy resin, vinyl chloride-vinyl acetate copolymer, polyamide resin, acrylic resin An insulating resin such as resin, polyacrylamide resin, polyvinyl pyridine resin, cellulose resin, urethane resin, casein, polyvinyl alcohol resin, or polyvinyl pyrrolidone resin may be contained. In this case, the insulating resin can be added at a desired ratio, thereby suppressing adhesion with the charge transport layer 6, coating film defects due to repelling, and the like.

  The protective layer 7 is formed by applying a coating liquid for forming a protective layer containing the above-described constituent materials on the charge transport layer 6 and curing it. Hereinafter, a method for forming the protective layer 7 will be described.

  When curing the oxetane compounds listed above, a general cationic polymerization initiator can be used in addition to heat. Preferable examples of these initiators include photocationic polymerization initiators such as diaryl iodonium salts and triaryl sulfonium salts.

  More specific examples of the cationic photopolymerization initiator include compounds represented by the following general formulas (C-1) to (C-4).

ここで、式（Ｃ−１）〜（Ｃ−４）中、Ｍは、アンチモン、ヒ素、リン又はホウ素を示し、これらのうちＭはリンであることが好ましい。また、式（Ｃ−１）〜（Ｃ−４）中、Ｘは、ハロゲンを示し、Ｘはフッ素であることが好ましい。また、式（Ｃ−１）〜（Ｃ−４）中、ｅはＭの価数を示し、例えば、Ｍがアンチモン、ヒ素、又はリンの場合はｅが５、Ｍがホウ素の場合はｅが３を意味する。また、式（Ｃ−１）中、Ｒ^４０は、水素原子、炭素数１〜１８のアルキル基、又は炭素数１〜１８のアルコキシ基を示す。また、式（Ｃ−２）中、Ｒ^４１は、水素原子、炭素数１〜１８のアルキル基、又は炭素数１〜１８のアルコキシ基を示す。また、式（Ｃ−４）中、Ｒ^４２は、水素原子、ヒドロキシアルキル基、又はヒドロキシアルコキシ基を示し、これらのうちＲ^４２はヒドロキシエトキシ基であることが好ましい。

Here, in formulas (C-1) to (C-4), M represents antimony, arsenic, phosphorus or boron, and among these, M is preferably phosphorus. In formulas (C-1) to (C-4), X represents halogen, and X is preferably fluorine. In the formulas (C-1) to (C-4), e represents the valence of M. For example, when M is antimony, arsenic, or phosphorus, e is 5, and when M is boron, e is Means 3. In Formula (C-1), R ⁴⁰ represents a hydrogen atom, an alkyl group having 1 to 18 carbon atoms, or an alkoxy group having 1 to 18 carbon atoms. In formula (C-2), R ⁴¹ represents a hydrogen atom, an alkyl group having 1 to 18 carbon atoms, or an alkoxy group having 1 to 18 carbon atoms. In formula (C-4), R ⁴² represents a hydrogen atom, a hydroxyalkyl group, or a hydroxyalkoxy group, and among these, R ⁴² is preferably a hydroxyethoxy group.

  The cationic photopolymerization initiator contained in the protective layer-forming coating solution is preferably 0.1 to 20% by mass, more preferably 0.1 to 10% by mass with respect to the oxetane compound. .

  Moreover, since it is preferable to contain the above-described charge transport material in the protective layer, it is preferable to add a catalyst to the coating solution for forming the protective layer, or to use the catalyst when preparing the coating solution for forming the protective layer. Examples of the catalyst used include inorganic acids such as hydrochloric acid, acetic acid, phosphoric acid and sulfuric acid, organic acids such as formic acid, propionic acid, oxalic acid, p-toluenesulfonic acid, benzoic acid, phthalic acid and maleic acid; diaryliodonium salts and tria Cation radical initiators such as reelsulfonium salts; alkaline catalysts such as potassium hydroxide, sodium hydroxide, calcium hydroxide, ammonia, triethylamine and the like. Furthermore, a solid catalyst insoluble in the system can also be used. These catalysts can be used alone or in combination of two or more.

  In addition, when adding a phenol derivative having a methylol group to the coating solution for forming the protective layer, in order to remove the catalyst at the time of synthesizing the phenol derivative, the phenol derivative is preliminarily mixed with an appropriate substance such as methanol, ethanol, toluene, ethyl acetate, It is preferable to dissolve in a solvent and perform treatment such as washing with water, reprecipitation using a poor solvent, or treatment using an ion exchange resin or an inorganic solid.

  Examples of the ion exchange resin include Amberlite 15, Amberlite 200C, Amberlist 15E (above, manufactured by Rohm and Haas); Dowex MWC-1-H, Dowex 88, Dowex HCR-W2 (and more) Levacit SPC-108, Levacit SPC-118 (above, Bayer); Diaion RCP-150H (Mitsubishi Kasei); Sumikaion KC-470, Duolite C26-C, Duolite C-433, Duolite-464 (above, manufactured by Sumitomo Chemical Co., Ltd.); Cation exchange resins such as Nafion-H (DuPont); Amberlite IRA-400, Amberlite IRA-45 (above, Rohm and Anion exchange resins such as (made by Haas) are listed.

Examples of the inorganic solid include an inorganic solid in which a group containing a protonic acid group such as Zr (O ₃ PCH ₂ CH ₂ SO ₃ H) ₂ and Th (O ₃ PCH ₂ CH ₂ COOH) ₂ is bonded to the surface. A polyorganosiloxane containing a protonic acid group such as a polyorganosiloxane having a sulfonic acid group; a heteropolyacid such as cobalt tungstic acid or phosphomolybdic acid; an isopolyacid such as niobic acid, tantalic acid or molybdic acid; silica gel, alumina, Single metal oxides such as chromia, zirconia, CaO, MgO; complex metal oxides such as silica-alumina, silica-magnesia, silica-zirconia, zeolites; clay minerals such as acid clay, activated clay, montmorillonite, and kaolinite ; LiSO _4, metal sulfates MgSO ₄ and the like; phosphoric acid zirconia, Li A group containing an amino group of a solid such as obtained by reacting aminopropyltriethoxysilane on silica gel surface; acid metal phosphate such as _{lanthanum; LiNO 3, Mn (NO 3} ) 2 and the like of a metal nitrate Bonded inorganic solids; polyorganosiloxanes containing amino groups such as amino-modified silicone resins.

  For the coating liquid for forming the protective layer, various alcohols such as methanol, ethanol, propanol and butanol; ketones such as acetone and methyl ethyl ketone; tetrahydrofuran; ethers such as diethyl ether and dioxane, etc. A solvent can be contained. In order to apply a dip coating method generally used for production of an electrophotographic photosensitive member, an alcohol solvent, a ketone solvent, or a mixed solvent thereof is preferable. Moreover, the boiling point of the solvent to be used is preferably 50 to 150 ° C., and these can be arbitrarily mixed and used.

  The solvent to be used is preferably an alcohol solvent, a ketone solvent, or a mixed solvent thereof. Therefore, the charge transport material contained in the protective layer 7 is preferably soluble in these solvents.

  The amount of the solvent contained in the coating liquid for forming the protective layer can be arbitrarily set. However, if the amount is too small, the constituent materials are likely to be precipitated, so the total amount of solids contained in the coating liquid for forming the protective layer is 1 mass part. On the other hand, it is preferable to set it as 0.5-30 mass parts, and it is more preferable to set it as 1-20 mass parts.

  In addition, in order to adjust film properties such as hardness, adhesiveness, and flexibility of the protective layer 7, terephthalic acid, maleic acid, pyromellitic acid, biphenyltetracarboxylic acid, etc., or the like May be further added. These addition amounts are preferably in a range where the influence on the electric characteristics is sufficiently small. Specifically, 0.05 to 1 part by weight is preferable with respect to 1 part by weight of the charge transport material, and 1-0.7 mass part is more preferable.

  When a phenol resin is mixed with the coating solution for protection formation, it is preferable to add a phenol resin curing catalyst. Examples of the curing catalyst include bissulfonyldiazomethanes such as bis (isopropylsulfonyl) diazomethane, bissulfonylmethanes such as methylsulfonyl p-toluenesulfonylmethane, and sulfonylcarbonyldiazomethanes such as cyclohexylsulfonylcyclohexylcarbonyldiazomethane. Sulfonylcarbonyl alkanes such as 2-methyl-2- (4-methylphenylsulfonyl) propiophenone, nitrobenzyl sulfonates such as 2-nitrobenzyl p-toluenesulfonate, alkyl such as pyrogallol trismethanesulfonate And aryl sulfonates (g) benzoin sulfonates such as benzoin tosylate, N- (trifluoromethylsulfonyloxy) phthali N-sulfonyloxyimides such as pyridine, pyridones such as (4-fluorobenzenesulfonyloxy) -3,4,6-trimethyl-2-pyridone, 2,2,2-trifluoro-1-trifluoro Photoacid generators such as sulfonic acid esters such as methyl-1- (3-vinylphenyl) -ethyl-4-chlorobenzenesulfonate, onium salts such as triphenylsulfonium methanesulfonate, diphenyliodonium trifluoromethanesulfonate, and protons Examples thereof include compounds obtained by neutralizing acids or Lewis acids with Lewis bases, mixtures of Lewis acids and trialkyl phosphates, sulfonate esters, phosphate esters, onium compounds, and carboxylic anhydride compounds.

Compounds obtained by neutralizing a protonic acid or Lewis acid with a Lewis base include halogenocarboxylic acids, sulfonic acids, sulfuric acid monoesters, phosphoric acid mono- and diesters, polyphosphoric acid esters, boric acid mono- and diesters, and the like. Various amines such as monoethylamine, triethylamine, pyridine, piperidine, aniline, morpholine, cyclohexylamine, n-butylamine, monoethanolamine, diethanolamine, triethanolamine, or trialkylphosphine, triarylphosphine, trialkylphosphite, triaryl Compounds neutralized with phosphite, as well as NureCure 2500X, 4167, X-47-110, 3525, 5225 commercially available as acid-base blocking catalysts (trade name, King Ndasutori Co., Ltd.), and the like. Examples of the compound obtained by neutralizing a Lewis acid with a Lewis base include compounds obtained by neutralizing a Lewis acid such as BF ₃ , FeCl ₃ , SnCl ₄ , AlCl ₃ , ZnCl ₂ with the above Lewis base.

  Examples of the onium compound include triphenylsulfonium methanesulfonate, diphenyliodonium trifluoromethanesulfonate, and the like.

  Examples of the carboxylic anhydride compound include acetic anhydride, propionic anhydride, butyric anhydride, isobutyric anhydride, lauric anhydride, oleic anhydride, stearic anhydride, n-caproic anhydride, n-caprylic anhydride, and n-capric anhydride. , Palmitic anhydride, myristic anhydride, trichloroacetic anhydride, dichloroacetic anhydride, monochloroacetic anhydride, trifluoroacetic anhydride, heptafluorobutyric anhydride, and the like.

  Examples of Lewis acids include boron trifluoride, aluminum trichloride, ferrous chloride, ferric chloride, ferrous chloride, ferric chloride, zinc chloride, zinc bromide, stannous chloride, and ferric chloride. Metal halides such as tin, stannous bromide and stannic bromide, organometallic compounds such as trialkyl boron, trialkyl aluminum, dialkyl aluminum halide, monoalkyl aluminum halide and tetraalkyl tin, diiso Propoxyethyl acetoacetate aluminum, tris (ethyl acetoacetate) aluminum, tris (acetylacetonato) aluminum, diisopropoxy bis (ethyl acetoacetate) titanium, diisopropoxy bis (acetylacetonato) titanium, tetrakis (n- Propyl acetoacetate) Luconium, tetrakis (acetylacetonato) zirconium, tetrakis (ethylacetoacetate) zirconium, dibutyl bis (acetylacetonato) tin, tris (acetylacetonato) iron, tris (acetylacetonato) rhodium, bis (acetylacetonato) Metal chelate compounds such as zinc and tris (acetylacetonato) cobalt, dibutyltin dilaurate, dioctyltin ester malate, magnesium naphthenate, calcium naphthenate, manganese naphthenate, iron naphthenate, cobalt naphthenate, copper naphthenate, naphthenic acid Zinc, zirconium naphthenate, lead naphthenate, calcium octylate, manganese octylate, iron octylate, cobalt octylate, zinc octylate, zirconium octylate, octylic acid 'S, lead octylate, zinc laurate, magnesium stearate, aluminum stearate, calcium stearate, cobalt stearate, zinc stearate, and metal soaps such as stearate lead. These may be used individually by 1 type and may be used in combination of 2 or more type. Among the organometallic compounds, aluminum metal compounds are particularly preferable because they are effective for oxetane compounds and epoxy resins.

  Although the usage-amount in particular of said phenol resin curing catalyst is not restrict | limited, 0.1-20 mass parts is preferable with respect to the total 100 mass parts of solid content contained in the coating liquid for protective layer formation, 0.3-10 Part by mass is particularly preferred.

  Moreover, when using the organometallic compound as a catalyst when forming the protective layer 7, it is preferable to add a polydentate ligand from the viewpoint of pot life and curing efficiency. Examples of such multidentate ligands include, but are not limited to, those shown below and those derived therefrom.

  Specifically, β-diketones such as acetylacetone, trifluoroacetylacetone, hexafluoroacetylacetone, and dipivaloylmethylacetone; acetoacetates such as methyl acetoacetate and ethyl acetoacetate; bipyridine and derivatives thereof; glycine and its Derivatives; ethylenediamine and derivatives thereof; 8-oxyquinoline and derivatives thereof; salicylaldehyde and derivatives thereof; catechol and derivatives thereof; bidentate ligands such as 2-oxyazo compounds; diethyltriamine and derivatives thereof; nitrilotriacetic acid and derivatives thereof And tridentate ligands such as ethylenediaminetetraacetic acid (EDTA) and derivatives thereof. In addition to the organic ligands as described above, inorganic ligands such as pyrophosphoric acid and triphosphoric acid can be exemplified. As the multidentate ligand, a bidentate ligand is particularly preferable, and specific examples include a bidentate ligand represented by the following general formula (XII-4) in addition to the above.

式（ＸＩＩ−４）中、Ｒ^４３及びＲ^４４はそれぞれ独立に、炭素数１〜１０のアルキル基、フッ化アルキル基、又は炭素数１〜１０のアルコキシ基を示す。

In formula (XII-4), R ⁴³ and R ⁴⁴ each independently represent an alkyl group having 1 to 10 carbon atoms, a fluorinated alkyl group, or an alkoxy group having 1 to 10 carbon atoms.

As the multidentate ligand, a bidentate ligand represented by the above general formula (XII-4) is preferably used, and R ⁴³ and R ^{44 in} the above general formula (XII-4) are the same. Is particularly preferred. By making R ⁴³ and R ^{44 the} same, the coordination power of the ligand near room temperature becomes strong, and the coating liquid for forming the protective layer can be further stabilized.

  As a coating method when forming the protective layer 7 using the coating liquid for forming the protective layer, blade coating method, wire bar coating method, spray coating method, dip coating method, bead coating method, air knife coating method, curtain coating Ordinary methods such as a method can be used. However, when a required film thickness cannot be obtained by a single application, the necessary film thickness can be obtained by applying a plurality of times. In addition, when performing the multiple application | coating several times, a heat processing may be performed every time of application | coating, and may be after carrying out multiple application | coating several times.

  After applying the coating liquid for forming the protective layer on the charge transport layer 6, the solvent is removed from the coating film by heating. Examples of heating conditions include 50 to 170 ° C. and 30 minutes to 2 hours.

  Subsequently, a curing process is further performed on the coated film. Examples of the curing treatment include a method using a thermal crosslinking reaction or a photocrosslinking reaction, or a combination thereof.

  When curing is performed by a thermal crosslinking reaction, the curing temperature is usually higher and the curing time is preferably longer in order to promote the crosslinking reaction of the coating film and increase the mechanical strength of the protective layer 7. However, in order to avoid alteration of the photoreceptor, it is preferable to appropriately control the curing temperature, curing time, crosslinking atmosphere or curing catalyst.

  As curing temperature, 100-170 degreeC is preferable, 100-150 degreeC is more preferable, and 100-140 degreeC is still more preferable. The curing time is preferably 30 minutes to 2 hours, more preferably 30 minutes to 1 hour. Curing can be performed in an air atmosphere or a nitrogen atmosphere.

  Further, when curing is performed by a photocrosslinking reaction, it is preferable that the light irradiation time is long. Examples of the light irradiation method include ultraviolet irradiation using a light source such as a mercury arc lamp, a xenon arc lamp, a fluorescent lamp, a carbon arc lamp, or a tungsten-halogen lamp.

  Moreover, when hardening by ultraviolet irradiation, it is possible to use typical photosensitizers, such as pyrene, perylene, acridine orange, thioxanthone, 2-chlorothioxanthone, and benzoflavin. In this case, the addition amount of the photosensitizer is preferably 0.05 to 1 part by mass and more preferably 0.1 to 0.7 part by mass with respect to 1 part by mass of the oxetane compound.

The light irradiation intensity is preferably 0.01 W / cm ² or more, and the light irradiation time is preferably 1 to 300 seconds, more preferably 5 to 100 seconds. Moreover, when using an electron beam, it can usually be hardened | cured with the energy of 300 eV or less, but when making it harden | cure instantaneously, it is also possible to carry out by 1Mrad-5Mrad.

  The above-described curing treatment can be performed in an air atmosphere or a nitrogen atmosphere. In the curing reaction of only a general epoxy resin, there is no difference in curing speed in both environments. However, when the coating liquid for forming a protective layer containing the oxetane compound according to the present invention is used, the curing treatment in a nitrogen atmosphere is performed by an epoxy. It is more preferable because an excellent curing rate can be obtained as compared with the curing rate of the resin alone.

  In the present embodiment, from the viewpoint of sufficient curing of the protective layer, after removing the solvent from the coating film of the protective layer forming coating solution, photocrosslinking reaction by ultraviolet irradiation, thermal crosslinking reaction by heating Are preferably performed in this order.

  The thickness of the protective layer 7 is preferably 0.5 to 15 μm, more preferably 1 to 10 μm, and more preferably 1 to 5 μm.

  In this embodiment, the outermost surface layer containing the resin having a crosslinked structure according to the present invention can be, for example, the charge transport layer 6 in the electrophotographic photoreceptor shown in FIG.

  In the case of constituting a single layer type photosensitive layer, the single layer type photosensitive layer is formed containing a charge generating material and a binder resin. The charge generation material is the same as that used for the charge generation layer in the function separation type photosensitive layer, and the binder resin is a binder resin used for the charge generation layer and the charge transport layer in the function separation type photosensitive layer. Similar ones can be used. The content of the charge generating material in the single-layer type photosensitive layer is preferably 10 to 85% by mass, more preferably 20 to 50% by mass, based on the total solid content in the single-layer type photosensitive layer. A charge transport material or a polymer charge transport material may be added to the single-layer type photosensitive layer for the purpose of improving photoelectric characteristics. The addition amount is preferably 5 to 50% by mass based on the total solid content in the single-layer type photosensitive layer. Moreover, the solvent and coating method used for coating can be the same as those for the above layers. The thickness of the single-layer type photosensitive layer is preferably about 5 to 50 μm, more preferably 10 to 40 μm.

  When the single-layer type photosensitive layer 8 is the outermost surface layer as in the electrophotographic photoreceptor 1 shown in FIG. 4, the oxetane resin having a crosslinked structure is included in this layer. The single-layer type photosensitive layer 8 includes a charge generation material, a charge transport material, an oxetane compound, a hydroxyl group, a carboxyl group, an alkoxysilyl group, an epoxy group, an oxetane group, a thiol group, and an amino group. It can be formed in the same manner as the protective layer 7 of the electrophotographic photosensitive member 1 shown in FIG. 2 using a coating liquid containing the above charge transporting material and other materials as necessary.

(Image forming device)
FIG. 6 is a schematic diagram showing a preferred embodiment of the image forming apparatus of the present invention. An image forming apparatus 100 shown in FIG. 6 includes a process cartridge 20 including an electrophotographic photosensitive member 1, an exposure device 30, a transfer device 40, and an intermediate transfer member 50 in an image forming apparatus main body (not shown). . In the image forming apparatus 100, the exposure device 30 is disposed at a position where the electrophotographic photosensitive member 1 can be exposed from the opening of the process cartridge 20, and the transfer device 40 is interposed between the electrophotographic photosensitive member via the intermediate transfer member 50. The intermediate transfer member 50 is disposed such that a part of the intermediate transfer member 50 can come into contact with the electrophotographic photosensitive member 1.

  The process cartridge 20 is obtained by integrating a charging device 21, a developing device 25, a cleaning device 27, and a fibrous member (toothbrush shape) 29 together with an electrophotographic photosensitive member 1 by a mounting rail in a case. The case is provided with an opening for exposure.

  Here, the charging device 21 charges the electrophotographic photosensitive member 1 by a contact method. The developing device 25 develops the electrostatic latent image on the electrophotographic photosensitive member 1 to form a toner image.

Hereinafter, the toner used for the developing device 25 will be described. The toner preferably has an average shape factor (ML ² / A) of 100 to 150, and more preferably 100 to 140. Further, the toner preferably has an average particle diameter of 2 to 12 μm, more preferably 3 to 12 μm, and even more preferably 3 to 9 μm. By using a toner satisfying such an average shape factor and average particle size, an image with high development, transferability and high image quality can be obtained.

  The toner is not particularly limited by the production method as long as it satisfies the above average shape factor and average particle diameter. For example, the toner may be a binder resin, a colorant and a release agent, and charged as necessary. A kneading and pulverizing method in which a control agent is added to knead, pulverizing, and classifying; a method of changing the shape of particles obtained by the kneading and pulverizing method with mechanical impact force or thermal energy; a polymerizable monomer for a binder resin Emulsion polymerization and agglomeration, and a dispersion of the formed dispersion and a dispersion of a colorant, a release agent, and a charge control agent as necessary are agglomerated and heat-fused to obtain toner particles. A suspension polymerization method in which a polymerizable monomer for obtaining a binder resin, a colorant, a release agent, and a charge control agent, if necessary, are suspended in an aqueous solvent and polymerized; the binder resin And a solution such as a colorant, a release agent, and a charge control agent as necessary in an aqueous solvent. Nigosa was toners produced by dissolution suspension method in which granulated are employed.

  Further, a known method such as a production method in which the toner obtained by the above method is used as a core, and agglomerated particles are further adhered and heat-fused to give a core-shell structure can be used. The toner production method is preferably a suspension polymerization method, an emulsion polymerization aggregation method, or a dissolution suspension method in which an aqueous solvent is used from the viewpoint of shape control and particle size distribution control, and an emulsion polymerization aggregation method is particularly preferable.

  The toner base particles are composed of a binder resin, a colorant, and a release agent, and include silica and a charge control agent as necessary.

  Binder resins used for toner base particles include styrenes such as styrene and chlorostyrene, monoolefins such as ethylene, propylene, butylene and isoprene, vinyl acetate, vinyl propionate, vinyl benzoate, vinyl butyrate, etc. Α-methylene aliphatics such as vinyl esters, methyl acrylate, ethyl acrylate, butyl acrylate, dodecyl acrylate, octyl acrylate, phenyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, dodecyl methacrylate Homopolymers and copolymers of monocarboxylic acid esters, vinyl ethers such as vinyl methyl ether, vinyl ethyl ether and vinyl butyl ether, vinyl ketones such as vinyl methyl ketone, vinyl hexyl ketone and vinyl isopropenyl ketone Polyester resins by copolymerization of dicarboxylic acids and diols.

  Particularly representative binder resins include polystyrene, styrene-alkyl acrylate copolymer, styrene-alkyl methacrylate copolymer, styrene-acrylonitrile copolymer, styrene-butadiene copolymer, styrene-maleic anhydride copolymer. A polymer, polyethylene, polypropylene, a polyester resin, etc. can be mentioned. In addition, polyurethane, epoxy resin, silicone resin, polyamide, modified rosin, paraffin wax and the like can also be mentioned.

  In addition, as colorants, magnetic powders such as magnetite and ferrite, carbon black, aniline blue, caryl blue, chrome yellow, ultramarine blue, Dupont oil red, quinoline yellow, methylene blue chloride, phthalocyanine blue, malachite green oxalate, Lamp Black, Rose Bengal, C.I. I. Pigment red 48: 1, C.I. I. Pigment red 122, C.I. I. Pigment red 57: 1, C.I. I. Pigment yellow 97, C.I. I. Pigment yellow 17, C.I. I. Pigment blue 15: 1, C.I. I. Pigment Blue 15: 3 can be exemplified as a representative one.

  Typical examples of the release agent include low molecular polyethylene, low molecular polypropylene, Fischer tropical wax, montan wax, carnauba wax, rice wax, and candelilla wax.

  As the charge control agent, known ones can be used, and azo metal complex compounds, metal complex compounds of salicylic acid, and resin type charge control agents containing polar groups can be used. When the toner is manufactured by a wet manufacturing method, it is preferable to use a material that is difficult to dissolve in water in terms of controlling ionic strength and reducing wastewater contamination. The toner may be either a magnetic toner containing a magnetic material or a non-magnetic toner containing no magnetic material.

  The toner used in the developing device 25 can be manufactured by mixing the toner base particles and the external additive with a Henschel mixer or a V blender. In addition, when the toner base particles are produced by a wet method, external addition can also be performed by a wet method.

  Lubricating particles may be added to the toner used in the developing device 25. Lubricating particles include solid lubricants such as graphite, molybdenum disulfide, talc, fatty acids and fatty acid metal salts, low molecular weight polyolefins such as polypropylene, polyethylene and polybutene, silicones having a softening point upon heating, oleic amides Aliphatic amides such as erucic acid amide, ricinoleic acid amide, stearic acid amide, etc., plant waxes such as carnauba wax, rice wax, candelilla wax, tree wax, jojoba oil, animals such as beeswax Minerals such as system waxes, montan waxes, ozokerites, ceresins, paraffin waxes, microcrystalline waxes, Fischer-Tropsch waxes, etc., petroleum waxes, and modified products thereof can be used. These can be used individually by 1 type or in combination of 2 or more types. However, the average particle size is preferably in the range of 0.1 to 10 μm, and the particles having the above chemical structure may be pulverized to make the particle sizes uniform. The amount added to the toner is preferably in the range of 0.05 to 2.0 mass%, more preferably 0.1 to 1.5 mass%.

  To the toner used in the developing device 25, inorganic fine particles, organic fine particles, composite fine particles obtained by attaching inorganic fine particles to the organic fine particles, and the like can be added for the purpose of removing deposits and deteriorated matters on the surface of the electrophotographic photosensitive member. .

  Inorganic fine particles include silica, alumina, titania, zirconia, barium titanate, aluminum titanate, strontium titanate, magnesium titanate, zinc oxide, chromium oxide, cerium oxide, antimony oxide, tungsten oxide, tin oxide, tellurium oxide, Various inorganic oxides such as manganese oxide, boron oxide, silicon carbide, boron carbide, titanium carbide, silicon nitride, titanium nitride, and boron nitride, nitrides, borides, and the like are preferably used.

  In addition, the inorganic fine particles are mixed with a titanium coupling agent such as tetrabutyl titanate, tetraoctyl titanate, isopropyl triisostearoyl titanate, isopropyl tridecylbenzenesulfonyl titanate, bis (dioctylpyrophosphate) oxyacetate titanate, γ- (2- Aminoethyl) aminopropyltrimethoxysilane, γ- (2-aminoethyl) aminopropylmethyldimethoxysilane, γ-methacryloxypropyltrimethoxysilane, N-β- (N-vinylbenzylaminoethyl) γ-aminopropyltrimethoxy Silane hydrochloride, hexamethyldisilazane, methyltrimethoxysilane, butyltrimethoxysilane, isobutyltrimethoxysilane, hexyltrimethoxysilane, octyltrimethoxy The treatment may be performed with a silane coupling agent such as silane, decyltrimethoxysilane, dodecyltrimethoxysilane, phenyltrimethoxysilane, o-methylphenyltrimethoxysilane, and p-methylphenyltrimethoxysilane. In addition, those hydrophobized with higher fatty acid metal salts such as silicone oil, aluminum stearate, zinc stearate and calcium stearate are also preferably used.

  Examples of the organic fine particles include styrene resin particles, styrene acrylic resin particles, polyester resin particles, and urethane resin particles.

  The particle diameter is preferably 5 nm to 1000 nm, more preferably 5 nm to 800 nm, and still more preferably 5 nm to 700 nm in terms of average particle diameter. If the average particle size is less than the lower limit, the polishing ability tends to be lacking. On the other hand, if the average particle size exceeds the upper limit, the surface of the electrophotographic photoreceptor tends to be damaged. Moreover, it is preferable that the sum of the addition amount of the particle | grains mentioned above and lubricity particle | grains is 0.6 mass% or more.

  Other inorganic oxides added to the toner are small-diameter inorganic oxides with a primary particle size of 40 nm or less for powder flowability, charge control, etc. It is preferable to add a larger-diameter inorganic oxide. These inorganic oxide fine particles may be known ones, but it is preferable to use silica and titanium oxide in combination for precise charge control. Further, the surface treatment of the small-diameter inorganic fine particles increases the dispersibility and increases the powder flowability. Furthermore, it is also preferable to add carbonates such as calcium carbonate and magnesium carbonate and inorganic minerals such as hydrotalcite in order to remove the discharge purified product.

  In addition, the color toner for electrophotography is used by mixing with a carrier. As the carrier, iron powder, glass beads, ferrite powder, nickel powder, or those having a resin coating on the surface thereof are used. The mixing ratio with the carrier can be set as appropriate.

  The cleaning device 27 includes a fibrous member (roll shape) 27a and a cleaning blade 27b.

Although the cleaning device 27 is provided with the fibrous member 27a and the cleaning blade 27b, the cleaning device 27 may be provided with either one. The fibrous member 27a may have a toothbrush shape in addition to the roll shape. Further, the fibrous member 27a may be fixed to the cleaning device main body, may be supported so as to be rotatable, and may be supported so as to be capable of oscillating in the photosensitive member axial direction. As the fibrous member 27a, polyester, nylon, acrylic, etc., cloth-like ones made of ultrafine fibers such as Toraysee (made by Toray Industries), resin fibers such as nylon, acrylic, polyolefin, polyester, etc. are used as a substrate or carpet. The brush-like thing etc. which were flocked to can be mentioned. Further, as the fibrous member 27a, a conductive powder or an ionic conductive agent is added to the above-described material to impart conductivity, or a conductive layer is formed inside or outside of each fiber. Can also be used. When conductivity is imparted, the resistance value is preferably 10 ² to 10 ⁹ Ω as a single fiber. The fiber thickness of the fibrous member 27a is preferably 30 d (denier) or less, more preferably 20 d or less, and the fiber density is preferably 20,000 fibers / inch ² or more, more preferably 30,000 fibers / inch. inch ² or more.

  The cleaning device 27 is required to remove deposits (for example, discharge products) on the surface of the photoreceptor with a cleaning blade and a cleaning brush. In order to achieve this purpose over a long period of time and stabilize the function of the cleaning member, the cleaning member may be supplied with a lubricating substance (lubricating component) such as metal soap, higher alcohol, wax, silicone oil or the like. preferable.

  For example, when a roll-shaped member is used as the fibrous member 27a, it is preferable to supply a lubricating component to the surface of the electrophotographic photosensitive member by bringing it into contact with a lubricating substance such as metal soap or wax. A normal rubber blade is used as the cleaning blade 27b. As described above, when a rubber blade is used as the cleaning blade 27b, supplying a lubricating component to the surface of the electrophotographic photosensitive member is particularly effective in suppressing chipping and wear of the blade.

  The process cartridge 20 described above is detachable from the image forming apparatus main body, and constitutes the image forming apparatus together with the image forming apparatus main body.

  The exposure device 30 may be any device that exposes the charged electrophotographic photosensitive member 1 to form an electrostatic latent image. Further, it is preferable to use a multi-beam surface emitting laser as the light source of the exposure apparatus 30.

  The transfer device 40 may be any device that transfers the toner image on the electrophotographic photosensitive member 1 to a transfer medium (intermediate transfer member 50). For example, a roll-shaped one that is usually used is used.

  As the intermediate transfer member 50, a belt-like member (intermediate transfer belt) such as polyimide, polyamideimide, polycarbonate, polyarylate, polyester, rubber or the like having semiconductivity is used. Further, as the form of the intermediate transfer member 50, a drum-like member can be used in addition to the belt-like member.

  When using the electrophotographic photoreceptor of the present invention, paper dust, talc, etc. are generated from the print paper, which easily adheres to the electrophotographic photoreceptor, and the electrophotographic photoreceptor of the present invention is resistant. It is difficult to remove paper dust, talc and the like because of its high wear resistance. Therefore, it is preferable to use the intermediate transfer member 50 in order to prevent adhesion of paper dust and talc and obtain a stable image.

  The transfer medium referred to in the present invention is not particularly limited as long as it is a medium to which a toner image formed on the electrophotographic photoreceptor 1 is transferred. For example, when transferring directly from the electrophotographic photosensitive member 1 to paper or the like, paper or the like is a transfer medium, and when the intermediate transfer member 50 is used, the intermediate transfer member is a transfer medium.

  FIG. 7 is a schematic view showing another embodiment of the image forming apparatus of the present invention. In the image forming apparatus 110 shown in FIG. 7, the electrophotographic photosensitive member 1 is fixed to the main body of the image forming apparatus, and the charging device 22, the developing device 25, and the cleaning device 27 are each formed into a cartridge. It is provided independently as a cleaning cartridge. Note that the charging device 22 includes a charging device for charging by a corona discharge method.

  In the image forming apparatus 110, the electrophotographic photosensitive member 1 and other apparatuses are separated, and the charging device 22, the developing device 25, and the cleaning device 27 are fixed to the image forming apparatus main body by screws, caulking, adhesion, or welding. It is possible to detach it by the operation by pulling out and pushing in without being done.

  Since the electrophotographic photosensitive member of the present invention is excellent in wear resistance, it may not be necessary to form a cartridge. Therefore, the charging device 22, the developing device 25, or the cleaning device 27 can be detached and attached by an operation by pulling out and pushing in without being fixed to the main body by screws, caulking, adhesion, or welding. The member cost per hit can be reduced. Also, two or more of these devices can be detachable as an integrated cartridge, thereby further reducing the member cost per print.

  The image forming apparatus 110 has the same configuration as that of the image forming apparatus 100 except that the charging device 22, the developing device 25, and the cleaning device 27 are each formed as a cartridge.

  FIG. 8 is a schematic diagram showing another embodiment of the image forming apparatus of the present invention. The image forming apparatus 120 is a tandem full-color image forming apparatus equipped with four process cartridges 20. In the image forming apparatus 120, four process cartridges 20 are arranged in parallel on the intermediate transfer member 50, and one electrophotographic photosensitive member can be used for one color. The image forming apparatus 120 has the same configuration as that of the image forming apparatus 100 except that it is a tandem system.

  In the tandem-type image forming apparatus 120, the amount of wear of each electrophotographic photosensitive member varies depending on the use ratio of each color, and thus the electrical characteristics of each electrophotographic photosensitive member tend to vary. Along with this, the toner development characteristics gradually change from the initial state, and the hue of the print image changes, so that a stable image cannot be obtained. In particular, in order to reduce the size of the image forming apparatus, a small-diameter electrophotographic photosensitive member tends to be used, and this tendency becomes remarkable when one having a diameter of 30 mmΦ or less is used. Here, when the configuration of the electrophotographic photosensitive member of the present invention is adopted as the electrophotographic photosensitive member, the surface wear is sufficiently suppressed even when the diameter is 30 mmΦ or less. Therefore, the electrophotographic photosensitive member of the present invention is particularly effective for a tandem type image forming apparatus.

  FIG. 9 is a schematic view showing another embodiment of the image forming apparatus of the present invention. The image forming apparatus 130 shown in FIG. 9 is a so-called four-cycle image forming apparatus that forms toner images of a plurality of colors with one electrophotographic photosensitive member. The image forming apparatus 130 includes a photosensitive drum 1 that is rotated by a driving device (not shown) at a predetermined rotational speed in the direction of arrow A in the figure, and above the photosensitive drum 1 is a photosensitive member. A charging device 22 for charging the outer peripheral surface of the drum 1 is provided.

  Further, an exposure device 30 having a surface emitting laser array as an exposure light source is disposed above the charging device 22. The exposure device 30 modulates a plurality of laser beams emitted from a light source in accordance with an image to be formed and deflects the laser beams in the main scanning direction so that the axis of the photosensitive drum 1 is on the outer peripheral surface of the photosensitive drum 1. Scan in parallel. Thereby, an electrostatic latent image is formed on the outer peripheral surface of the charged photosensitive drum 1.

  A developing device 25 is disposed on the side of the photosensitive drum 1. The developing device 25 includes a roller-shaped container that is rotatably arranged. Four containers are formed inside the container, and developing units 25Y, 25M, 25C, and 25K are provided in each container. The developing devices 25Y, 25M, 25C, and 25K each include a developing roller 26, and store Y, M, C, and K color toners therein.

  The full-color image is formed by the image forming apparatus 130 while the photosensitive drum 1 is rotated four times. That is, while the photosensitive drum 1 rotates four times, the charging device 22 charges the outer peripheral surface of the photosensitive drum 1, and the exposure device 20 includes Y, M, C, and K image data representing a color image to be formed. Scanning the outer peripheral surface of the photosensitive drum 1 with the laser beam modulated according to any one of the above is repeated while switching the image data used for modulation of the laser beam every time the photosensitive drum 1 rotates. Further, the developing device 25 operates the developing device corresponding to the outer peripheral surface in a state where any of the developing rollers 26 of the developing devices 25Y, 25M, 25C, and 25K corresponds to the outer peripheral surface of the photosensitive drum 1. The photosensitive drum 1 is the one that develops the electrostatic latent image formed on the outer peripheral surface of the photosensitive drum 1 to a specific color and forms a toner image of the specific color on the outer peripheral surface of the photosensitive drum 1. Each time it rotates, the process is repeated while rotating the container so that the developing unit used for developing the electrostatic latent image is switched. As a result, every time the photosensitive drum 1 rotates, the Y, M, C, and K toner images are sequentially formed on the outer peripheral surface of the photosensitive drum 1 so as to overlap each other. When the drum 1 rotates four times, a full-color toner image is formed on the outer peripheral surface of the photosensitive drum 1.

  An endless intermediate transfer belt 50 is disposed substantially below the photosensitive drum 1. The intermediate transfer belt 50 is wound around rollers 51, 53, and 55, and is disposed so that the outer peripheral surface is in contact with the outer peripheral surface of the photosensitive drum 1. The rollers 51, 53, and 55 are rotated by a driving force of a motor (not shown) and rotate the intermediate transfer belt 50 in the direction of arrow B in FIG.

  A transfer device (transfer device) 40 is disposed on the opposite side of the photosensitive drum 1 across the intermediate transfer belt 50, and the toner image formed on the outer peripheral surface of the photosensitive drum 1 is intermediate transferred by the transfer device 40. The image is transferred onto the image forming surface of the belt 50.

  A lubricant supply device 29 and a cleaning device 27 are disposed on the outer peripheral surface of the photosensitive drum 1 on the opposite side of the developing device 25 with the photosensitive drum 1 interposed therebetween. When the toner image formed on the outer peripheral surface of the photoconductive drum 12 is transferred to the intermediate transfer belt 50, the lubricant is supplied to the outer peripheral surface of the photoconductive drum 1 by the lubricant supply device 29. The area carrying the transferred toner image is cleaned by the cleaning device 27.

  A tray 60 is disposed below the intermediate transfer belt 50, and a large number of sheets P as recording materials are accommodated in the tray 60 in a stacked state. A take-out roller 61 is disposed obliquely above and to the left of the tray 60, and a roller pair 63 and a roller 65 are arranged in this order on the downstream side in the take-out direction of the paper P by the take-out roller 61. The uppermost recording sheet in the stacked state is taken out from the tray 60 by the take-out roller 61 rotating, and is conveyed by the roller pair 63 and the roller 65.

  A transfer device 42 is disposed on the opposite side of the roller 55 with the intermediate transfer belt 50 interposed therebetween. The paper P conveyed by the roller pair 63 and the roller 65 is sent between the intermediate transfer belt 50 and the transfer device 42, and the toner image formed on the image forming surface of the intermediate transfer belt 50 is transferred by the transfer device 42. . A fixing device 44 having a pair of fixing rollers is arranged on the downstream side of the transfer device 42 in the conveyance direction of the paper P. The paper P on which the toner image is transferred is transferred by the fixing device 44. After being fused and fixed, the sheet is discharged out of the image forming apparatus 130 and placed on a discharge tray (not shown).

  EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited to these Examples. In the following examples, “part” means part by mass.

<Production of photoconductor>
(Photoreceptor 1)
First, a 30 mmφ cylindrical aluminum substrate was prepared. This aluminum substrate was polished by a centerless polishing apparatus, and the surface roughness was set to Rz = 0.6 μm. In order to clean the aluminum base material subjected to the centerless polishing treatment, degreasing treatment, etching treatment with 2 wt% sodium hydroxide solution for 1 minute, neutralization treatment, and pure water washing were performed in this order. Next, an anodic oxide film (current density 1.0 A / dm ² ) was formed on the surface of the aluminum base material with a 10 wt% sulfuric acid solution. After washing with water, sealing treatment was performed by dipping in a 1 wt% nickel acetate solution at 80 ° C. for 20 minutes. Further, pure water washing and drying treatment were performed. In this way, an aluminum base material having a 7 μm anodic oxide film formed on the surface was obtained.

  Next, chlorogallium phthalocyanine having strong diffraction peaks at Bragg angles (2θ ± 0.2 °) of 7.4 °, 16.6 °, 25.5 ° and 28.3 ° in the X-ray diffraction spectrum is 1 Parts, polyvinyl butyral (ESREC BM-S, manufactured by Sekisui Chemical Co., Ltd.) and 100 parts of n-butyl acetate are mixed and treated with a glass shaker with a paint shaker for 1 hour and dispersed to form a coating for forming a charge generation layer A liquid was obtained. This coating solution was dip coated on the obtained aluminum substrate and dried by heating at 100 ° C. for 10 minutes to form a charge generation layer having a thickness of about 0.15 μm.

  Next, 2.5 parts of a benzidine compound represented by the following formula (XIII-1), 3 parts of a polymer compound having a structural unit represented by the following formula (XIII-2) (viscosity average molecular weight 39,000) and 20 parts of chlorobenzene was mixed and dissolved to obtain a coating solution for forming a charge transport layer.

ＣＴ−１

CT-1

  This coating solution was applied onto the charge generation layer by a dip coating method and heated at 115 ° C. for 40 minutes to form a charge transport layer having a thickness of 20 μm. In this way, the photoreceptor in which the charge generation layer and the charge transport layer were formed on the aluminum base material on which the anodized film was formed was designated as “photoreceptor 1”.

(Photoreceptor 2)
First, a 30 mmφ cylindrical aluminum base material subjected to a honing treatment was prepared. Next, 100 parts of a zirconium compound (trade name: Olgatrix ZC540, manufactured by Matsumoto Pharmaceutical Co., Ltd.), 10 parts of a silane compound (trade name: A1100, manufactured by Nihon Unicar Co., Ltd.), 400 parts of isopropanol, and 200 parts of butanol are mixed. Thus, a coating solution for forming the undercoat layer was obtained. This coating solution was dip-coated on an aluminum substrate and dried by heating at 150 ° C. for 8 minutes to form an undercoat layer having a thickness of 0.1 μm.

  Next, the Bragg angle (2θ ± 0.2 °) in the X-ray diffraction spectrum is 7.5 °, 9.9 °, 12.5 °, 16.3 °, 18.6 °, 25.1 ° and Mix 1 part of hydroxygallium phthalocyanine with a strong diffraction peak at 28.3 °, 1 part of polyvinyl butyral (ESREC BM-S, manufactured by Sekisui Chemical Co., Ltd.), and 100 parts of n-butyl acetate, and paint with glass beads. Dispersion was carried out with a shaker for 1 hour to obtain a coating solution for forming a charge generation layer. This coating solution was dip-coated on the undercoat layer and dried by heating at 100 ° C. for 10 minutes to form a charge generation layer having a thickness of about 0.15 μm.

  Next, 2 parts of a charge transport material represented by the following formula (XIII-3), 3 parts of a polymer compound having a structural unit represented by the above formula (XIII-2) (viscosity average molecular weight 50,000), and 20 parts of chlorobenzene was mixed to obtain a coating solution for forming a charge transport layer.

  This coating solution was applied onto the charge generation layer by a dip coating method and heated at 115 ° C. for 40 minutes to form a charge transport layer having a thickness of 20 μm. In this way, the photoreceptor in which the undercoat layer, the charge generation layer, and the charge transport layer were formed on the honing-treated aluminum base material was designated as “photoreceptor 2”.

(Synthesis of charge transport material represented by the above formula (III-17))
10 parts of N, N'-diphenyl-N, N'-bis (3-humanoxyphenyl)-(1,1'-bisphenol) -4,4'-diamine, 50 parts of toluene, 2 parts of sodium hydroxide powder 0.0 part and 1 part of triethylamine were mixed and stirred for 1 hour. To this, 20 parts of 3-chloromethyl-3-ethyloxetane was added over 1 hour, stirred at room temperature for 8 hours, and then heated at 50 ° C. for 1 hour for reaction. The obtained reaction product was washed with water and then purified by silica gel chromatography to obtain 5.6 g of a charge transport material represented by the above formula (III-17). The IR spectrum of this charge transport material is shown in FIG.

Example 1
7 parts of an oxetane compound represented by the following formula (VII-1) (trade name “OXT-221” manufactured by Toa Gosei Co., Ltd.), 0.2 part of diphenyl-4-thiophenoxyphenylsulfonium antimonate, the above formula 5 parts of the charge transport material represented by (II-23) and 15 parts of isopropyl alcohol were mixed to obtain a coating solution for forming a protective layer.

This coating solution was applied onto the charge transport layer of the photoreceptor 1 by a dip coating method and dried at 80 ° C. for 15 minutes in a nitrogen atmosphere to form a coating film having a thickness of 3 μm. Next, this coating film was irradiated with ultraviolet rays having an irradiation intensity of 25 mW / cm ² for 40 seconds in a nitrogen atmosphere, and then heated and cured at 130 ° C. for 1 hour to form a protective layer. The obtained photoreceptor was designated as PR-1.

(Example 2)
2 parts of 3-ethyl-3-oxetanemethanol represented by the following formula (VI-1), 6 parts of resol type phenol resin (PL-4852, manufactured by Gunei Chemical Co., Ltd.), diphenyl-4-thiophenoxyphenyl sulfone Coating for forming a protective layer by mixing 0.2 parts of nium antimonate, 0.03 parts of methylphenylpolysiloxane, 5 parts of the charge transport material represented by the above formula (I-2), and 15 parts of isopropyl alcohol A liquid was obtained.

This coating solution was applied onto the charge transport layer of the photoreceptor 1 by a dip coating method and dried at 80 ° C. for 15 minutes in a nitrogen atmosphere to form a coating film having a thickness of 3 μm. Next, this coating film was irradiated with ultraviolet rays having an irradiation intensity of 25 mW / cm ² for 40 seconds in a nitrogen atmosphere, and then heated and cured at 130 ° C. for 1 hour to form a protective layer. The obtained photoreceptor is referred to as PR-2.

(Example 3)
5 parts of an oxetane compound of the following formula (VI-5) (trade name “OXT-211” manufactured by Toa Gosei Co., Ltd.), 2 parts of an epoxy compound represented by the following formula (XIII-4), and the above formula (II-58) ), 5 parts of charge transport material, 0.2 part of diphenyl-4-thiophenoxyphenylsulfonium antimonate, and 15 parts of isopropyl alcohol were mixed to obtain a coating solution for forming a protective layer.

This coating solution was applied onto the charge transport layer of the photoreceptor 1 by a dip coating method and dried at 80 ° C. for 15 minutes in a nitrogen atmosphere to form a coating film having a thickness of 3 μm. Next, this coating film was irradiated with ultraviolet rays having an irradiation intensity of 25 mW / cm ² for 40 seconds in a nitrogen atmosphere, and then heated and cured at 130 ° C. for 1 hour to form a protective layer. The obtained photoreceptor is referred to as PR-3.

Example 4
5 parts of an oxetane compound represented by the following formula (VI-12) (trade name “OXT-610” manufactured by Toagosei Co., Ltd.), 5 parts of a charge transport material represented by the above formula (III-17), and isopropyl alcohol 15 parts, 9 parts of tetrahydrofuran, and 0.9 parts of distilled water were mixed and dissolved. To this solution, 0.5 part of an ion exchange resin (Amberlyst 15E) was added, followed by hydrolysis at room temperature for 1 hour.

  With respect to the liquid obtained by filtering and separating the ion exchange resin from the reaction mixture after hydrolysis, 0.1 part of aluminum trisacetylacetonate (Al (aqaq) 3), 0.1 part of acetylacetonate, the following formula (XIII-5) 0.2 parts of the epoxy compound represented by the above and diphenyl-4-thiophenoxyphenylsulfonium antimonate were mixed to obtain a coating solution for forming a protective layer.

This coating solution was applied onto the charge transport layer of the photoreceptor 1 by a dip coating method and dried at 80 ° C. for 15 minutes in a nitrogen atmosphere to form a coating film having a thickness of 3 μm. Next, this coating film was irradiated with ultraviolet rays having an irradiation intensity of 25 mW / cm ² for 40 seconds in a nitrogen atmosphere, and then heated and cured at 130 ° C. for 1 hour to form a protective layer. The obtained photoreceptor is referred to as PR-4.

(Example 5)
A protective layer was formed in the same manner as in Example 1 except that the photoconductor 2 was used instead of the photoconductor 1. The obtained photoreceptor is referred to as PR-5.

(Example 6)
A protective layer was formed in the same manner as in Example 2 except that the photoconductor 2 was used instead of the photoconductor 1. The obtained photoreceptor is referred to as PR-6.

(Example 7)
A protective layer was formed in the same manner as in Example 3 except that the photoconductor 2 was used instead of the photoconductor 1. The obtained photoreceptor is referred to as PR-7.

(Example 8)
A protective layer was formed in the same manner as in Example 4 except that the photoconductor 2 was used instead of the photoconductor 1. The obtained photoreceptor is referred to as PR-8.

Example 9
In the coating liquid for forming a protective layer of Example 1, the amount of the oxetane compound represented by the above formula (VII-1) was changed to 5 parts, and 2 parts of bisglycidyl bisphenol A was further added. Thus, a protective layer was formed. The obtained photoreceptor is referred to as PR-9.

(Comparative Example 1)
8 parts of resol type phenol resin (PL-4852, manufactured by Gunei Chemical Co., Ltd.), 0.2 parts of diphenyl-4-thiophenoxyphenylsulfonium antimonate, 0.03 parts of methylphenylpolysiloxane, 5 parts of the charge transport material represented by I-2) and 15 parts of isopropyl alcohol were mixed to obtain a coating solution for forming a protective layer.

  This coating solution was applied on the charge transport layer of the photoreceptor 1 by a dip coating method and dried at 140 ° C. for 40 minutes in a nitrogen atmosphere to form a protective layer having a thickness of 3 μm. The obtained photoreceptor is referred to as PR-10.

(Comparative Example 2)
In the coating liquid for forming a protective layer of Example 3, Example 3 was used except that an epoxy compound represented by the following formula (XIII-6) was blended instead of the oxetane compound represented by the above formula (VI-5). Similarly, a protective layer was formed. The obtained photoreceptor is referred to as PR-11.

(Comparative Example 3)
In the coating liquid for forming a protective layer of Example 3, Example 3 except that an epoxy compound represented by the above formula (XIII-4) was blended instead of the oxetane compound represented by the above formula (VI-5). Similarly, a protective layer was formed. The obtained photoreceptor is referred to as PR-12.

<Image formation test>
The photoreceptors (PR-1) to (PR-12) were subjected to an image formation test using an image forming apparatus (manufactured by Fuji Xerox Co., Ltd., DocuCenter Color 400CP). That is, first, an image forming test for 10,000 sheets is performed in an environment of low temperature and low humidity (10 ° C., 20% RH), and then, 10,000 sheets in an environment of high temperature and high humidity (28 ° C., 75% RH). An image formation test was conducted. Thereafter, evaluation was made with respect to deposits on the photoreceptor, cleaning properties, wear rate, and image quality. The results obtained are shown in Table 48.

  In addition, about the deposit | attachment, it judged and evaluated by the criteria of A: No adhesion, B: Partial adhesion (about 30% or less of the whole), and C: Adhesion. In addition, regarding the cleanability, the evaluation is made based on the criteria of A: good, B: partial (about 10% or less of the whole) image defects such as streaks, and C: extensive image defects. did. As for the wear rate, the amount of wear of the photoconductor was measured and calculated as the wear rate per 1000 revolutions. Regarding the image quality, the print image quality after a total of 20,000 prints was visually evaluated based on the criteria of A: good, C1: extremely low image density, and C2: streak-like defects.

  From the results shown in Table 48, it was confirmed that the photoconductors of the examples were excellent in electrical characteristics and that surface adhesion did not remain even after long-term use, and the image forming apparatus using the photoconductors of the examples had high image quality and long length. It was confirmed that the lifetime could be realized.

1 is a schematic cross-sectional view showing a preferred embodiment of an electrophotographic photoreceptor of the present invention. FIG. 6 is a schematic cross-sectional view showing another preferred embodiment of the electrophotographic photosensitive member of the present invention. FIG. 6 is a schematic cross-sectional view showing another preferred embodiment of the electrophotographic photosensitive member of the present invention. FIG. 6 is a schematic cross-sectional view showing another preferred embodiment of the electrophotographic photosensitive member of the present invention. FIG. 6 is a schematic cross-sectional view showing another preferred embodiment of the electrophotographic photosensitive member of the present invention. 1 is a schematic diagram showing a preferred embodiment of an image forming apparatus of the present invention. It is a schematic diagram which shows other suitable embodiment of the image forming apparatus of this invention. It is a schematic diagram which shows other suitable embodiment of the image forming apparatus of this invention. It is a schematic diagram which shows other suitable embodiment of the image forming apparatus of this invention. It is IR spectrum of the electric charge transport material shown by general formula (III-17) used in the Example.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 ... Electrophotographic photosensitive member, 2 ... Conductive support body, 3 ... Photosensitive layer, 4 ... Undercoat layer, 5 ... Charge generation layer, 6 ... Charge transport layer, 7 ... Protective layer, 8 ... Single layer type photosensitive layer, 20 Process cartridge, 100, 110, 120, 130 Image forming apparatus.

Claims (6)

Comprising a conductive substrate and a photosensitive layer provided on the conductive substrate;
The photosensitive layer has an outermost surface layer containing a resin having a crosslinked structure on the side farthest from the conductive substrate; and
The resin, Ri oxetane resin der containing oxetane compound as a resin component,
The outermost surface layer further includes a charge transport material having at least one functional group selected from a hydroxyl group, a carboxyl group, an alkoxysilyl group, an epoxy group, an oxetane group, a thiol group, and an amino group. Photoconductor. 2. The electrophotographic photoreceptor according to claim 1 , wherein the charge transport material is at least one selected from compounds represented by the following general formula (I), (II), or (III).
F-[(X ¹ ) _m ^1- (R ¹ ) _{m 2} -Y] _{m 3} (I)
[In Formula (I), F represents an organic group derived from a compound having a hole transporting ability, X ¹ represents an oxygen atom or a sulfur atom, R ¹ represents an alkylene group, Y represents a hydroxyl group, a carboxyl group, or a thiol group. Or an amino group, m1 and m2 each independently represent 0 or 1, and m3 represents an integer of 1 to 4. ]
_{^{F - [(X 2) n1}} - (R 2) n2 - (Z) n3 G] n4 (II)
[In the formula (II), F represents an organic group derived from a compound having a hole transporting ability, X ² represents an oxygen atom or a sulfur atom, R ² represents an alkylene group, Z represents an oxygen atom, a sulfur atom, NH Or COO, G represents an epoxy group or oxetane group, n1, n2 and n3 each independently represents 0 or 1, and n4 represents an integer of 1 to 4. ]
F- [D-Si (R ³ ) _(3-a) Q _a ] _b (III)
[In Formula (III), F represents an organic group derived from a compound having a hole transporting ability, D represents a divalent group having flexibility, and R ³ represents a hydrogen atom, a substituted or unsubstituted alkyl group. Alternatively, a substituted or unsubstituted aryl group, Q is a hydrolyzable group, a is an integer of 1 to 3, and b is an integer of 1 to 4. ] The oxetane resin, electrophotographic photosensitive member according to claim 1 or claim 2, further comprising an epoxy compound as a resin component. The electrophotographic photoreceptor according to any one of claims 1 to 3 , wherein the oxetane resin further contains a phenol derivative having a methylol group as a resin component. An electrophotographic photosensitive member according to any one of claims 1-4,
A charging device for charging the electrophotographic photosensitive member;
An exposure apparatus that exposes the charged electrophotographic photosensitive member to form an electrostatic latent image;
A developing device for developing the electrostatic latent image to form a toner image;
A transfer device for transferring the toner image to a transfer target;
An image forming apparatus comprising: The electrophotographic photosensitive member according to any one of claims 1 to 4 ,
It is selected from a charging device for charging the electrophotographic photosensitive member, a developing device for developing a latent electrostatic image formed by exposure to form a toner image, and a cleaning device for removing toner remaining on the electrophotographic photosensitive member. At least one,
A process cartridge comprising:

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