JP2018072373A - Electrophotographic photoreceptor, image forming apparatus, and method for manufacturing electrophotographic photoreceptor - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an electrophotographic photoreceptor that has a protective layer formed of a polymerization cured product having a high charge transport ability, and small in blade torque.SOLUTION: An electrophotographic photoreceptor according to the present invention comprises a conductive substrate, a photosensitive layer, and a protective layer. The protective layer is formed of a polymerization cured product obtained through a radical reaction of a racial polymerizable composition including a radical polymerizable monomer, a perfluoropolyether compound having a radical polymerizable functional group, insulating metal oxide particles having a radical polymerizable functional group, and a charge transport compound.SELECTED DRAWING: None

Description

  The present invention relates to an electrophotographic photoreceptor, an image forming apparatus having the electrophotographic photoreceptor, and a method for producing the electrophotographic photoreceptor.

  In an electrophotographic image forming apparatus, an electrophotographic photosensitive member (hereinafter also simply referred to as “photosensitive member”) is used to form an electrostatic latent image corresponding to an image to be formed. The surface of the photoreceptor is charged by a charging member of the image forming apparatus. The electrostatic latent image is formed by irradiating light on the surface of a charged photoreceptor. When toner is supplied to the photoreceptor on which the electrostatic latent image is formed, a toner image is formed. The toner image is transferred to a recording medium. The toner remaining on the surface of the photoreceptor after the transfer is removed by a cleaning member of the image forming apparatus.

  As the photosensitive member, a photosensitive member having a conductive support, a photosensitive layer disposed on the conductive support, and a protective layer disposed on the photosensitive layer is known. As the photoreceptor, a photoreceptor having a protective layer containing inorganic particles is known from the viewpoint of increasing the film strength of the protective layer (see, for example, Patent Documents 1 and 2). The protective layer of the photoreceptor described in Patent Document 1 is composed of a polymerized cured product of a polymerizable composition containing silica particles having a polymerizable unsaturated group and a polymerizable compound having the polymerizable unsaturated group. ing. The protective layer of the photoreceptor described in Patent Document 2 includes a specific charge transport compound, silica particles, tin oxide having a polymerizable unsaturated group, and a polymerizable compound having the polymerizable unsaturated group. It is comprised with the polymeric hardened | cured material of polymeric composition.

JP 2010-014948 A JP 2014-002364 A

  Although it is preferable from the viewpoint of film strength, abrasion resistance, and scratch resistance, it is preferable from the viewpoint of electrical characteristics that the protective layer is composed of a polymerized cured product as in the photoreceptors described in Patent Documents 1 and 2. It may not be enough. In particular, when trying to satisfy the image quality required for color printing, a transfer memory may be generated. On the other hand, when the protective layer contains a charge transport compound as in the photoreceptor described in Patent Document 2, although the generation of the transfer memory can be suppressed, the charge transport compound acts as a plasticizer. When there is too much content of the charge transport compound in the protective layer, the film strength of the protective layer may be insufficient.

  In addition, when the protective layer contains conductive particles as inorganic particles, the content of the charge transport compound can be reduced, but the electric field strength in the protective layer is reduced and sufficient charge transport capability is obtained. As a result, a transfer memory may be generated. In general, since the cured film has a large frictional force against the cleaning member, so-called blade torque, when images with high coverage are continuously printed, the lubricant of the protective layer is removed, resulting in scratches in the protective layer. As a result, defective cleaning may occur. Thus, in a photoreceptor in which the protective layer is composed of a cured film containing inorganic particles and a charge transport compound, there is still room for study from the viewpoint of achieving both the electrical characteristics, wear resistance, and cleaning properties of the protective layer. Has been.

  A first object of the present invention is to provide an electrophotographic photosensitive member having a protective layer composed of a polymerized cured film having a high charge transport capability and a low blade torque. A second object of the present invention is to provide an image forming apparatus capable of suppressing the occurrence of image defects due to defective cleaning over a long period of time.

  As a means for solving the first problem, an electrophotographic photosensitive member according to the present invention includes a conductive support, a photosensitive layer disposed on the conductive support, and a photosensitive layer. And a protective layer disposed thereon. The protective layer includes a radical polymerizable monomer, a perfluoropolyether compound having a radical polymerizable functional group, insulating metal oxide particles having a radical polymerizable functional group, and a charge transport compound. It is composed of a polymerized cured product obtained by radical reaction of the composition.

  In order to solve the second problem, an image forming apparatus according to the present invention includes an electrophotographic photosensitive member and cleaning for removing transfer residual toner on the electrophotographic photosensitive member in contact with the electrophotographic photosensitive member. And a device. The electrophotographic photoreceptor is the electrophotographic photoreceptor according to the present invention.

  As another means for solving the first problem, the method for producing an electrophotographic photoreceptor according to the present invention comprises applying a radical polymerizable composition containing a radical polymerizable monomer onto a photosensitive layer, and A step of forming a coating film of the radical polymerizable composition on the layer, and a step of irradiating the coating film with an actinic ray to polymerize the radical polymerizable monomer to form a protective layer. The radical polymerizable composition includes a radical polymerizable monomer, a perfluoropolyether compound having a radical polymerizable functional group, insulating metal oxide particles having a radical polymerizable functional group, and a charge transport compound. A radically polymerizable composition is used.

  According to the present invention, it is possible to provide an electrophotographic photosensitive member having a protective layer composed of a polymerized cured film having a high charge transport capability and a low blade torque. In addition, according to the present invention, it is possible to provide an image forming apparatus that can suppress the occurrence of image defects due to poor cleaning over a long period of time.

1A and 1B are schematic views showing the configuration of a circular slide hopper coating apparatus. FIG. 2 is a schematic diagram showing an example of the configuration of the image forming apparatus according to the embodiment of the present invention.

[Configuration of electrophotographic photoreceptor]
The electrophotographic photosensitive member (photosensitive member) according to the present embodiment includes a conductive support, an intermediate layer disposed on the conductive support, a photosensitive layer disposed on the intermediate layer, and the photosensitive member. And a protective layer disposed on the layer. The photoconductor can be configured in the same manner as a known photoconductor except for the protective layer.

  The conductive support is a member that can support the photosensitive layer and has conductivity. Examples of the conductive support include a metal drum or sheet, a plastic film having a laminated metal foil, a plastic film having a deposited conductive material film, a conductive material or a binder resin. A metal member having a conductive layer formed by applying a paint, a plastic film, paper, and the like are included. Examples of the metal include aluminum, copper, chromium, nickel, zinc, and stainless steel. Examples of the conductive material include the metal, indium oxide, and tin oxide.

  The intermediate layer is a layer having a barrier function and an adhesive function that is disposed between the conductive support and the photosensitive layer. The intermediate layer includes, for example, a binder resin and metal oxide particles. The number average primary particle size of the metal oxide particles is, for example, preferably 0.3 μm or less, and more preferably 0.1 μm or less. The content of the metal oxide particles is, for example, preferably 20 to 400 parts by mass, and more preferably 50 to 350 parts by mass with respect to 100 parts by mass of the binder resin in the intermediate layer.

  The thickness of the intermediate layer is preferably 0.1 to 15 μm, and more preferably 0.3 to 10 μm.

  The photosensitive layer is a layer for forming an electrostatic latent image corresponding to an intended image on the surface of the photoreceptor by exposure described later. The photosensitive layer may be composed of a single layer or a plurality of stacked layers. Examples of the photosensitive layer include a single layer containing a charge transport compound and a charge generation compound, and a laminate of a charge generation layer containing a charge generation compound and a charge transport layer containing a charge transport compound. included. The photosensitive layer of the photoreceptor according to the present embodiment is a laminate of a charge generation layer and a charge transport layer.

  When the photosensitive layer is the monolayer product, the thickness of the photosensitive layer is, for example, 10 to 50 μm, more preferably 20 to 40 μm. When the photosensitive layer is the laminate, the thickness of the charge generation layer is, for example, 0.01 to 5 μm, and more preferably 0.05 to 3 μm. Moreover, the thickness of the said charge transport layer is 5-40 micrometers, for example, More preferably, it is 10-30 micrometers.

  The protective layer is a layer for protecting the photosensitive layer. The protective layer is disposed on the photosensitive layer and constitutes the surface of the photoreceptor. The protective layer includes a radical polymerizable monomer, a perfluoropolyether compound having a radical polymerizable functional group, insulating metal oxide particles having a radical polymerizable functional group, and a charge transport compound. It is composed of a polymerized cured product obtained by radical reaction of the composition. That is, the protective layer is composed of an integral polymer obtained by radical polymerization of the radical polymerizable monomer, and contains a perfluoropolyether compound, insulating metal oxide particles, and a charge transport compound. Both the perfluoropolyether compound and the insulating metal oxide particles are bonded to the polymer by a covalent bond by radical polymerization.

  As described above, the protective layer is a polymerized cured product of the radical polymerizable composition, and the radical polymerizable composition includes a radical polymerizable monomer, a perfluoropolyether compound having a radical polymerizable functional group, and , Insulating metal oxide particles having a radical polymerizable functional group, and a charge transport compound. Any of these components may be one kind or more. Hereinafter, each component contained in the radical polymerizable composition will be described.

(Radically polymerizable monomer)
The radical polymerizable monomer has a radical polymerizable functional group, and is radically polymerized (cured) by being irradiated with an actinic ray such as ultraviolet ray, visible ray, electron beam, far infrared ray, etc., and is generally a binder for the protective layer. It is a compound that becomes a resin used as a resin. Examples of radically polymerizable monomers include styrene monomers, acrylic monomers, methacrylic monomers, vinyl toluene monomers, vinyl acetate monomers, and N-vinyl pyrrolidone monomers. Examples of the binder resin include polystyrene and polyacrylate.

The radical polymerizable functional group is a group having a carbon-carbon double bond and capable of radical polymerization. The radical polymerizable functional group is particularly preferably a (meth) acryloyl group because it can be cured with a small amount of light or in a short time. In the present specification, “(meth) acryloyl group” is a radical polymerizable functional group, and one of acryloyl group (CH ₂ ═CHCO—) and methacryloyl group (CH ₂ ═C (CH ₃ ) CO—). Or both.

  Specific examples of the radical polymerizable monomer include compounds represented by the following formulas M1 to M11. In the following formula, R represents an acryloyl group, and R ′ represents a methacryloyl group.

  The radical polymerizable monomer compound may be a known compound or a commercially available product. The radical polymerizable monomer preferably has three or more radical polymerizable functional groups from the viewpoint of forming a protective layer having a high crosslink density and a high hardness.

(Perfluoropolyether compound having a radical polymerizable functional group)
The perfluoropolyether part (hereinafter also referred to as “PFPE”) in the perfluoropolyether compound having the radical polymerizable functional group (hereinafter also referred to as “radical polymerizable PFPE”) is a repeating unit of perfluoroalkylene ether. As an oligomer or polymer.

  Examples of the structure of the repeating unit of perfluoroalkylene ether include perfluoromethylene ether, perfluoroethylene ether, and perfluoropropylene ether. The perfluoropolyether preferably has a repeating structural unit 1 represented by the following formula (a) or a repeating structural unit 2 represented by the following formula (b).

  When the PFPE has the repeating structural unit 1 or the repeating structural unit 2, the repeating number m of the repeating structural unit 1 and the repeating number n of the repeating structural unit 2 are each an integer of 0 or more, and m + n ≧ 1.

  Moreover, when it has both the said repeating structural unit 1 and the said repeating structural unit 2, this repeating structural unit 1 and this repeating structural unit 2 may form the block copolymer structure, or a random copolymer A structure may be formed.

  The weight average molecular weight Mw of the PFPE is preferably 100 or more and 8,000 or less, and more preferably 500 or more and 5,000 or less.

  The number of radical polymerizable functional groups possessed by the radical polymerizable PFPE is 1 or more, preferably 4 or more. When the radical polymerizable PFPE has two or more radical polymerizable functional groups, the position of the radical polymerizable functional group in the PFPE may be one end or both ends, and two or more radical polymerizable functional groups may be one end. May be bonded to each other, or may be bonded to both ends.

  Among these, radically polymerizable PFPE having four or more radically polymerizable functional groups has more reactive points with the above radically polymerizable monomer and radically polymerizable insulating particles described later. It is particularly preferable that the radical polymerizable PFPE has four or more radical polymerizable functional groups from the viewpoint of improving the wear resistance, scratch resistance and cleaning properties of the photoreceptor.

  The radical polymerizable functional group is a group having a carbon-carbon double bond and capable of radical polymerization, like the radical polymerizable monomer. The radical polymerizable functional group of the radical polymerizable PFPE may be the same as or different from that of the radical polymerizable monomer. In addition, the plurality of radical polymerizable functional groups possessed by the radical polymerizable PFPE may be the same as or different from each other. The radical polymerizable functional group is particularly preferably a (meth) acryloyl group.

  Examples of radically polymerizable PFPE having a (meth) acryloyl group include Fluorolink AD1700, MD500, MD700, 5101X, 5113X, Fomblin MT70 ("FLUOROLINK" and "FOMBLIN" manufactured by Solvay Specialty Polymers) Trademark), OPTOOL DAC manufactured by Daikin Industries, Ltd., and KY-1203 manufactured by Shin-Etsu Chemical Co., Ltd.

  In addition, radically polymerizable PFPE can be appropriately synthesized from PFPE having a terminal hydroxyl group or carboxyl group as a raw material by substitution of these substituents or induction from these substituents. It may be a product.

  Examples of PFPE having a hydroxyl group at the end include Fomblin D2, Fluorolink D4000, Fluorolink E10H, 5158X, 5147X, Fomblin Ztetraol manufactured by Solvay Specialty Polymers, and Demnum-SA manufactured by Daikin Industries, Ltd. Examples of PFPE having a carboxyl group at the terminal include FomblinZDIZAC4000 manufactured by Solvay Specialty Polymers and Demnum-SH manufactured by Daikin Industries, Ltd.

  Specific examples of PFPE having a (meth) acryloyl group include compounds represented by the following formulas P-1 to P-9. In the following formula, X represents an acryloyl group (A) or a methacryloyl group (M). Moreover, “p” in Compound P-2 independently represents 1 to 10.

  When X is an acryloyl group, A is added to the compound symbol when X is a methacryloyl group, whereby the following compounds are more specifically shown. For example, a compound of the following P-1 in which X is an acryloyl group is represented as “P-1A”, and a compound of the following P-1 in which a methacryloyl group is represented as “P-1M”.

  The specific example of the synthesis method of radically polymerizable PFPE is shown below.

(Synthesis Example 1 Synthesis of P-2M)
Perfluoropolyether compound Fluorolink E10H (manufactured by Solvay Specialty Polymers, Inc .: average molecular weight 1700) represented by the following formula P-S1, having hydroxyl groups at both ends, 17 parts by mass, triethylamine 3 parts by mass, diisopropyl ether 10 parts by mass, and Then, 0.006 part by mass of a polymerization inhibitor p-methoxyphenol is mixed, and stirring is started under an air stream. While maintaining the temperature of the mixed solution at 10 ° C., 3.1 parts by weight of methacrylic acid chloride is dropped over 2 hours. After completion of the dropwise addition, the resulting mixture is stirred for 1 hour while maintaining at 10 ° C. Next, the reaction solution is heated to 30 ° C., stirred at 30 ° C. for 1 hour, further heated to 50 ° C., and stirred at 50 ° C. for 10 hours to carry out the reaction. Next, 72 parts by mass of diisopropyl ether is added to the obtained reaction solution, and the diisopropyl ether phase is washed with water three times. The diisopropyl ether phase is then dehydrated with magnesium sulfate and the solvent is distilled off. In this way, P-2M which is radically polymerizable PFPE is obtained (yield 17.1 parts by mass).

(Synthesis Example 2 Synthesis of P-3M)
(1) Synthesis of intermediate (I) 18.5 parts by mass of perfluoropolyether compound Fomblin ZDIAC4000 (Solvay Specialty Polymers, Inc .: average molecular weight 3700) represented by the following formula P-S2 and having carboxyl groups at both ends , 20 parts by weight of thionyl chloride and 2 drops of N, N-dimethylformamide are mixed and heated to reflux for 4 hours. Excess thionyl chloride is distilled off from the resulting reaction solution to obtain 18.6 parts by mass of intermediate (I).

(2) Synthesis of P-3M Obtained by dissolving 2.3 parts by mass of glycerol dimethacrylate, 0.8 parts by mass of pyridine, and 0.006 parts by mass of polymerization inhibitor p-methoxyphenol in 50 parts by mass of dichloroethane. 18.6 parts by weight of intermediate (I) are added to the solution. The resulting mixture is allowed to stir overnight at room temperature and then water is added to separate the dichloroethane phase. The dichloroethane phase is washed with water and the solvent is distilled off. In this way, P-3M which is radically polymerizable PFPE is obtained (yield 20.2 parts by mass).

(Synthesis Example 3 Synthesis of P-6A)
Perfluoropolyether compound Fomblin Z-tet-raol (manufactured by Solvay Specialty Polymers) having hydroxyl groups at both ends, represented by the following formula P-S3, 0.01 parts by mass of polymerization inhibitor p-methoxyphenol Then, 0.01 parts by mass of the urethanization catalyst dibutyltin dilaurate and 20 parts by mass of methyl ethyl ketone are mixed, stirred under an air stream, and the mixture is heated to 80 ° C. Next, 5.7 parts by mass of 2- (acryloyloxy) ethyl isocyanate is divided and added to the above mixture while paying attention to heat generation. Next, the reaction is carried out by stirring the mixture at 80 ° C. for 10 hours. After confirming the disappearance of the absorption peak near 2360 cm ⁻¹ derived from the isocyanate group by IR spectrum measurement, the solvent is distilled off from the above mixture. In this way, P-6A which is radically polymerizable PFPE is obtained (yield 25.6 parts by mass).

Other exemplary compounds among the compounds P-1 to P-9 can be similarly synthesized by any of the following methods.
1) A method in which (meth) acrylic acid chloride is esterified by dehydrochlorination with a perfluoropolyether having a hydroxyl group at the terminal.
2) A method in which an isocyanate compound having a (meth) acryloyl group is subjected to a urethanization reaction with a perfluoropolyether having a hydroxyl group at the terminal.
3) A method in which a perfluoropolyether compound having a carboxyl group at the terminal is converted into an acid halide by a conventional method, and a compound having a (meth) acryloyl group and a hydroxyl group is esterified with the acid halide.

  If the content of the radical polymerizable PFPE in the protective layer is too small, the cleaning property of the photoreceptor is insufficient, and if too large, the film strength, abrasion resistance and scratch resistance of the photoreceptor may be insufficient. . From the viewpoint of sufficiently expressing the cleaning property of the photoreceptor, the content of the radical polymerizable PFPE is preferably 1 part by volume or more with respect to 100 parts by volume of the protective layer. Further, from the viewpoint of sufficiently exhibiting the wear resistance and scratch resistance, the content of the radical polymerizable PFPE is preferably 10 parts by volume or less with respect to 100 parts by volume of the protective layer.

(Insulating metal oxide particles having radical polymerizable groups)
The insulating metal oxide particles having a radical polymerizable group (hereinafter also referred to as “radical polymerizable insulating particles”) are insulating particles having a component containing a radical polymerizable functional group supported on the surface. The loading of the component containing the radical polymerizable functional group on the surface of the insulating particles may be physical loading or chemical bonding. The radical polymerizable functional group may be one kind or more.

  The radical polymerizable insulating particles include, for example, insulating metal oxide particles, a surface treatment agent residue chemically bonded to the surface thereof, and the radical polymerizable functional group contained in the surface treatment agent residue. In the protective layer, the insulating metal oxide particles are chemically bonded to the integral polymer constituting the protective layer via the surface treatment agent residue on the surface. Exists. The surface treating agent residue is, for example, a molecular structure that is chemically bonded to the surface of the insulating metal oxide particles and is a portion derived from the surface treating agent.

From the viewpoint of obtaining the desired electric field strength in the protective layer, the volume resistivity of the insulating metal oxide particles is preferably as large as possible, and the relative dielectric constant of the insulating metal oxide particles is as small as possible. The volume resistivity is preferably 10 ¹⁰ to 10 ¹⁶ Ω · cm, for example. The relative dielectric constant is preferably 3 to 10, for example. The volume resistivity and the relative dielectric constant can be determined based on the material of the insulating metal oxide particles.

  Examples of the material of the insulating metal oxide particles include silica (silicon oxide), alumina (aluminum oxide), and titanium oxide. Among them, the relative dielectric constant is small, the electric field loss of the protective layer due to the charging of the insulating metal oxide particles can be suppressed, the refractive index is small, the transparency of the protective layer can be ensured, the specific gravity From the viewpoint of dispersion stability of the insulating metal oxide particles in the dispersant during the production of the photoreceptor, the material of the insulating metal oxide particles is preferably silica. The insulating metal oxide particles may be one kind or more.

  Examples of the silica include dry method silica, wet precipitation method silica, and wet gel method silica. The silica particles may be hydrophilic silica particles having a silanol group, or may be hydrophobic silica particles that have been subjected to a hydrophobic treatment. Examples of the hydrophobizing treatment include trimethylsilylation of the silanol group and surface treatment of silica particles with silicone oil. Further, the silica particles may be one kind or more.

  The silica particles may be a synthetic product or a commercial product. Examples of commercially available silica particles include Aerosil R-972 manufactured by Nippon Aerosil Co., Ltd. (“Aerosil” is a registered trademark of the company, hereinafter omitted), R-974, R-976S, R-9200, RX-50, NAX-50, NX-90G, RX-200, R-8200, RX-300, R-812S, R-812, RY-50, NY-50, RY-200S, RY-200, RY- 200L, RY-300, NKT-90 and T-805; CAB-O-SIL TG-6110G manufactured by Cabot Corporation ("CAB-O-SIL" is a registered trademark of the company, hereinafter omitted), TG-810G TG-811F, TG-308F and TG-7580F; H2000 / 4, H2000T, H05TM, H13TM, H20TM, H3 manufactured by Clariant It includes and X-24-9163A manufactured by Shin-Etsu Chemical Co., Ltd.; TM, H05TD, H13TD, H20TD and H30TD.

  The number average primary particle size and content of the radical polymerizable insulating particles in the protective layer are substantially equal to the number average primary particle size and content of the insulating metal oxide particles, respectively. For this reason, the number average primary particle size and content of the radical polymerizable insulating particles can be determined by measuring the number average primary particle size and content of the insulating metal oxide particles, respectively.

  The number average primary particle size of the radical polymerizable insulating particles (the insulating metal oxide particles) is preferably 20 to 50 nm, for example. If the number average primary particle size of the radical polymerizable insulating particles is too small, sufficient wear resistance may not be obtained. When the number average primary particle size of the radical polymerizable insulating particles is too large, the radical polymerizable insulating particles are dispersed in a dispersion when the radical polymerizable insulating particles are dispersed in a solvent during the formation of the protective layer. Of the photosensitive member may be difficult to produce.

  The number average primary particle size of the radical polymerizable insulating particles (the insulating metal oxide particles) can be determined as follows, for example. A 10,000 times magnified photograph taken by a scanning electron microscope (manufactured by JEOL Ltd.) is taken into a scanner, and 300 particle images excluding agglomerated particles are randomly extracted from the obtained photograph image, and an automatic image processing analysis system. Using the “Luzex AP” (manufactured by Nireco Corporation, “LUZEX” is a registered trademark of the company, software Ver. 1.32), binarization processing was performed to calculate the horizontal ferret diameter of each particle image. The average value is calculated as the number average primary particle size. Here, the horizontal ferret diameter means the length of a side parallel to the x-axis of the circumscribed rectangle when the particle image is binarized.

  The number average primary particle size of the radical polymerizable insulating particles is included in the protective layer such as the radical polymerizable insulating particles, the charge transport compound, and the radical scavenger from the viewpoint of the film strength of the protective layer. It can be appropriately adjusted according to the components and their contents.

  The component containing the radical polymerizable functional group can be supported on the surface of the insulating metal oxide particles by, for example, a known surface treatment method using a known surface treating agent for the insulating metal oxide particles. .

  The surface treatment agent has a radical polymerizable functional group and a surface treatment functional group. The surface treatment agent may be one kind or more. The surface treatment functional group is a group having reactivity to a polar group such as a hydroxyl group present on the surface of the insulating metal oxide particle. The radical-polymerizable functional group is a radical-polymerizable group having a carbon-carbon double bond similar to that of the radical-polymerizable monomer or radical-polymerizable PFPE. Examples thereof include a vinyl group and (meth) acryloyl. A group is included.

  The surface treatment agent is preferably a silane coupling agent having the radical polymerizable functional group, and examples thereof include compounds represented by the following formulas S-1 to S-31.

_{S-1: CH 2 = CHSi} (CH 3) (OCH 3) 2
_{S-2: CH 2 = CHSi} (OCH 3) 3
S-3: CH ₂ = CHSiCl _{3
S-4: CH 2 = CHCOO} (CH 2) 2 Si (CH 3) (OCH 3) 2
_{S-5: CH 2 = CHCOO} (CH 2) 2 Si (OCH 3) 3
_{S-6: CH 2 = CHCOO} (CH 2) 2 Si (OC 2 H 5) (OCH 3) 2
_{S-7: CH 2 = CHCOO} (CH 2) 3 Si (OCH 3) 3
_{S-8: CH 2 = CHCOO} (CH 2) 2 Si (CH 3) Cl 2
_{S-9: CH 2 = CHCOO} (CH 2) 2 SiCl 3
_{S-10: CH 2 = CHCOO} (CH 2) 3 Si (CH 3) Cl 2
S-11: CH ₂ = CHCOO (CH ₂ ) ₃ SiCl _{3
S-12: CH 2 = C} (CH 3) COO (CH 2) 2 Si (CH 3) (OCH 3) 2
_{S-13: CH 2 = C} (CH 3) COO (CH 2) 2 Si (OCH 3) 3
_{S-14: CH 2 = C} (CH 3) COO (CH 2) 3 Si (CH 3) (OCH 3) 2
_{S-15: CH 2 = C} (CH 3) COO (CH 2) 3 Si (OCH 3) 3
_{S-16: CH 2 = C} (CH 3) COO (CH 2) 2 Si (CH 3) Cl 2
_{S-17: CH 2 = C} (CH 3) COO (CH 2) 2 SiCl 3
_{S-18: CH 2 = C} (CH 3) COO (CH 2) 3 Si (CH 3) Cl 2
_{S-19: CH 2 = C} (CH 3) COO (CH 2) 3 SiCl 3
_{S-20: CH 2 = CHSi} (C 2 H 5) (OCH 3) 2
_{S-21: CH 2 = C} (CH 3) Si (OCH 3) 3
_{S-22: CH 2 = C} (CH 3) Si (OC 2 H 5) 3
_{S-23: CH 2 = CHSi} (OCH 3) 3
_{S-24: CH 2 = C} (CH 3) Si (CH 3) (OCH 3) 2
_{S-25: CH 2 = CHSi} (CH 3) Cl 2
_{S-26: CH 2 = CHCOOSi} (OCH 3) 3
_{S-27: CH 2 = CHCOOSi} (OC 2 H 5) 3
_{S-28: CH 2 = C} (CH 3) COOSi (OCH 3) 3
_{S-29: CH 2 = C} (CH 3) COOSi (OC 2 H 5) 3
_{S-30: CH 2 = C} (CH 3) COO (CH 2) 3 Si (OC 2 H 5) 3
_{S-31: CH 2 = CHCOO} (CH 2) 2 Si (CH 3) 2 (OCH 3)

  The treatment amount of the surface treatment agent for the insulating metal oxide particles can be appropriately adjusted according to the number average primary particle size of the insulating metal oxide particles and the type of the surface treatment agent. The amount of the treatment is, for example, preferably 0.1 to 200 parts by mass, and more preferably 7 to 70 parts by mass with respect to 100 parts by mass of the insulating metal oxide particles.

  The content of the radically polymerizable insulating particles (the insulating metal oxide particles) in the protective layer can be appropriately adjusted within a range in which the effect of the present embodiment can be obtained. If the content is too small, the protective layer may not have the desired film strength and electrical resistance. On the other hand, if the content is too large, the presence of hydroxyl groups remaining on the surfaces of the insulating metal oxide particles may cause image flow to occur easily under high temperature and high humidity. From these viewpoints, the content of the radical polymerizable insulating particles in the protective layer is preferably 10 to 20 parts by volume with respect to 100 parts by volume of the protective layer.

(Charge transport compound)
The charge transport compound can adjust the electrical resistance of the protective layer. The charge transport compound may be appropriately selected from known compounds as long as the function can be exhibited. From the viewpoint of obtaining the desired film strength and electrical resistance for the protective layer, the charge transport compound is preferably a compound represented by the following general formula (1).

In the above general formula (1), R ¹ , R ² , R ³ , R ⁴ and R ⁵ are each a hydrogen atom, an alkyl group having 1 to 4 carbon atoms or an alkoxy group, and Ar ¹ is a hydrogen atom , An aromatic group having a substituent or an unsubstituted aromatic group, and Ar ² is an aromatic group having a substituent or an unsubstituted aromatic group.

  Specific examples of the charge transport compound represented by the general formula (1) include compounds represented by the following formulas T1 to T64.

  The content of the charge transport compound can be appropriately adjusted according to the desired film strength and electrical characteristics of the protective layer. If the content of the charge transfer agent is too small, desired electrical characteristics cannot be obtained, and the generation of the transfer memory may not be suppressed. If the content of the charge transfer agent is too large, the desired film strength may not be obtained. The content of the charge transfer agent is, for example, 10 to 35 parts by volume, and more preferably 15 to 25 parts by volume.

  The thickness of a protective layer is 2-15 micrometers, for example, More preferably, it is 4-8 micrometers.

  In the protective layer, the radical polymerizable monomer, the radical polymerizable PFPE, the radical polymerizable insulating particles, and the charge transport compound constitute an integral polymer (polymerized cured product) that forms the protective layer. Yes. The polymerization cured product is a polymer of the radical polymerizable monomer, the radical polymerizable PFPE, and the radical polymerizable insulating particles, and the charge transport compound is contained in the polymer, thermal decomposition GC-MS, It can be confirmed by analysis of the polymerized cured product by a known instrumental analysis technique such as nuclear magnetic resonance (NMR), Fourier transform infrared spectrophotometer (FT-IR), or elemental analysis.

[Method for producing photoreceptor]
The photoconductor can be produced by a known method for producing a photoconductor except that the radical polymerizable composition is used for the coating material for the protective layer. For example, the photoreceptor according to the present embodiment can be manufactured by a method including the following steps 1 to 4.
Step 1: Applying a coating liquid for forming an intermediate layer (hereinafter also referred to as “coating liquid 1”) on the outer peripheral surface of the conductive support to form a coating film of the coating liquid 1, and drying the coating film By doing so, an intermediate layer is formed.
Step 2: A coating solution for forming a charge generation layer (hereinafter also referred to as “coating solution 2”) is applied on the outer peripheral surface of the intermediate layer formed on the conductive support to form a coating film of the coating solution 2 The charge generation layer is formed by forming and drying the coating film.
Step 3: A coating liquid for forming a charge transport layer (hereinafter also referred to as “coating liquid 3”) is applied on the outer peripheral surface of the charge generation layer formed on the intermediate layer to form a coating film of the coating liquid 3 The charge transport layer is formed by forming and drying the coating film.
Step 4: Applying a coating liquid for forming a protective layer (the radical polymerizable composition) on the outer peripheral surface of the charge transport layer formed on the charge generation layer to form a coating film of the coating liquid, A protective layer is formed by curing the coating film.

(Step 1: Formation of intermediate layer)
First, a binder resin for an intermediate layer is dissolved in a solvent to prepare a coating solution 1 for forming an intermediate layer. From the viewpoint of adjusting the resistance of the intermediate layer, conductive metal oxide particles or insulating metal oxide particles may be dispersed in the coating liquid 1. Next, the coating liquid 1 is applied on the conductive support so as to have a certain thickness, and a coating film of the coating liquid 1 is formed on the conductive support. Next, the intermediate layer is formed by drying the coating film.

  Examples of the dispersing means for dispersing the metal oxide particles in the coating liquid 1 include an ultrasonic disperser, a ball mill, a sand mill, and a homomixer.

  Examples of the coating method of the coating liquid 1 include a dip coating method, a spray coating method, a spinner coating method, a bead coating method, a blade coating method, a beam coating method, a slide hopper method, and a circular slide hopper method.

  The method for drying the coating film of the coating liquid 1 can be appropriately selected according to the type of solvent and the thickness of the intermediate layer. The method for drying the coating film of the coating liquid 1 is preferably, for example, heat drying.

  The solvent in the coating liquid 1 is only required to disperse the metal oxide particles well and dissolve the binder resin for the intermediate layer. Examples of the solvent in the coating liquid 1 include alcohols having 1 to 4 carbon atoms such as methanol, ethanol, n-propyl alcohol, isopropyl alcohol, n-butanol, t-butanol, sec-butanol and the like. It is preferable that the solvent in the coating liquid 1 is the alcohol from the viewpoints of solubility of the binder resin and coating properties.

  Examples of the binder resin for the intermediate layer in the coating liquid 1 include casein, polyvinyl alcohol, nitrocellulose, ethylene-acrylic acid copolymer, polyamide, polyurethane, and gelatin. Among these, the binder resin for the intermediate layer is preferably an alcohol-soluble polyamide. The density | concentration of the said binder resin for intermediate | middle layers in the coating liquid 1 can be suitably adjusted according to the thickness, production rate, etc. of an intermediate | middle layer.

  Examples of the metal oxide constituting the metal oxide particles in the coating liquid 1 include aluminum oxide (alumina), zinc oxide, titanium oxide, tin oxide, antimony oxide, indium oxide, and bismuth oxide.

  From the viewpoint of the storage stability of the coating liquid 1 and the dispersibility of the metal oxide particles, the coating liquid 1 may further contain a cosolvent. Examples of the cosolvent include benzyl alcohol, toluene, methylene chloride, cyclohexanone and tetrahydrofuran.

(Step 2: Formation of charge generation layer)
First, a charge generation compound is dispersed in a solution in which a binder resin for a charge generation layer is dissolved in a solvent to prepare a coating solution 2 for forming a charge generation layer. Next, the coating liquid 2 is applied on the intermediate layer so as to have a certain thickness, and a coating film of the coating liquid 2 is formed on the intermediate layer. Next, the charge generation layer is formed by drying the coating film.

  An example of the dispersing means for dispersing the charge generating compound in the coating liquid 2 is the same as the dispersing means for dispersing the metal oxide particles in the coating liquid 1. An example of a method for applying the coating liquid 2 is the same as the method for applying the coating liquid 1. Further, the method for drying the coating film of the coating liquid 2 is the same as the method for drying the coating film of the coating liquid 1.

  Examples of the solvent in the coating solution 2 include toluene, xylene, methylene chloride, 1,2-dichloroethane, methyl ethyl ketone, cyclohexane, ethyl t-butyl acetate, methanol, ethanol, propanol, butanol, methyl cellosolve, 4-methoxy-4 -Methyl-2-pentanone, ethyl cellosolve, tetrahydrofuran, 1,4-dioxane, 1,3-dioxolane, pyridine and diethylamine are included.

  Examples of the binder resin for the charge generation layer in the coating solution 2 include polystyrene resin, polyethylene resin, polypropylene resin, acrylic resin, methacrylic resin, vinyl chloride resin, vinyl acetate resin, polyvinyl butyral resin, epoxy resin, polyurethane resin, Phenol resin, polyester resin, alkyd resin, polycarbonate resin, silicone resin, melamine resin, copolymer resin containing two or more of these resins (for example, vinyl chloride-vinyl acetate copolymer resin, vinyl chloride-vinyl acetate) -Maleic anhydride copolymer resin), and poly-vinylcarbazole resin.

  Examples of charge generating compounds include azo raw materials such as Sudan Red and Diane Blue; quinone pigments such as pyrenequinone and anthanthrone; quinocyanine pigments; perylene pigments; indigo pigments such as indigo and thioindigo; and phthalocyanine pigments.

  The content of the charge generating compound is preferably 1 to 600 parts by mass, and more preferably 50 to 500 parts by mass with respect to 100 parts by mass of the binder resin.

(Step 3: Formation of charge transport layer)
First, the charge transport layer forming coating solution 3 is prepared by dissolving the binder resin for the charge transport layer and the aforementioned charge transport compound in a solvent. Next, the coating liquid 3 is applied on the charge generation layer so as to have a certain thickness, and a coating film of the coating liquid 3 is formed on the charge generation layer. Next, the charge transport layer is formed by drying the coating film.

  An example of the coating method of the coating liquid 3 is the same as the coating method of the coating liquid 1. Further, the method for drying the coating film of the coating liquid 3 is the same as the method for drying the coating film of the coating liquid 1.

  Examples of the solvent in the coating liquid 3 are the same as those in the coating liquid 2.

  Examples of the binder resin in the coating liquid 3 include polycarbonate resin, polyacrylate resin, polyester resin, polystyrene resin, styrene-acrylonitrile copolymer resin, polymethacrylic ester resin, and styrene-methacrylic ester copolymer resin, Is included.

  The content of the charge transport compound is preferably 10 to 500 parts by mass and more preferably 20 to 100 parts by mass with respect to 100 parts by mass of the binder resin.

(Step 4: Formation of protective layer)
First, a radically polymerizable monomer, a perfluoropolyether compound having a radically polymerizable functional group, an insulating metal oxide particle having a radically polymerizable functional group, and a charge transport compound are added to a solvent for protection. A coating solution for layer formation (the aforementioned radically polymerizable composition) is prepared. At this time, if necessary, other components (for example, a radical polymerization initiator and a radical scavenger) may be further added to the radical polymerizable composition. Next, the prepared radical polymerizable composition is applied onto the charge transport layer to form a coating film of the radical polymerizable composition. Subsequently, the said coating film is dried, actinic light is irradiated, a radically polymerizable monomer is polymerized, and the said protective film is formed by hardening the said coating film.

  The protective layer is a reaction of the radical polymerizable monomers in the process of coating, drying, and curing, and a radical polymerizable functional group of the perfluoropolyether compound and the insulating metal oxide particles, The reaction with the radical polymerizable monomer proceeds to form a cross-linked curable resin.

  The content of the insulating metal oxide particles in the radical polymerizable composition is, for example, with respect to 100 parts by mass of all monomers (polyfunctional radical polymerizable compound and monofunctional radical polymerizable compound) for forming the cured resin. 10 to 35 parts by mass, preferably 15 to 25 parts by mass.

  The content of the charge transport compound in the radical polymerizable composition is, for example, 50 to 100 parts by mass of all monomers (polyfunctional radical polymerizable compound and monofunctional radical polymerizable compound) for forming the cured resin. It is preferably 250 parts by mass, more preferably 70 to 200 parts by mass, and particularly preferably 80 to 150 parts by mass.

  An example of a dispersing means for dispersing the insulating metal oxide particles and the charge transport compound in the radical polymerizable composition is the same as the dispersing means for dispersing the metal oxide particles in the coating liquid 1. Moreover, the example of the coating method of a radically polymerizable composition is the same as the coating method of the coating liquid 1. The application method of the radically polymerizable composition is preferably a circular slide hopper method. In this case, the radically polymerizable composition is applied using a circular slide hopper application device. Hereinafter, the application | coating method of the radically polymerizable composition using a circular slide hopper coating device is demonstrated.

  1A and 1B are schematic views showing the configuration of a circular slide hopper coating apparatus. As shown in FIGS. 1A and 1B, the circular slide hopper coating apparatus includes an annular coating head 260 provided so as to surround a cylindrical substrate 251, a storage tank 254 for storing the coating liquid L, Have Here, the base material 251 is a base material to which the coating liquid L is applied. For example, the base material in a state where the intermediate layer and the photosensitive layer are formed on the conductive support (before the protective layer is formed). Base material).

  The coating head 260 has a narrow coating liquid distribution slit 262 having a coating liquid outlet 261 that is open to the substrate 251 side, along the direction perpendicular to the longitudinal direction of the substrate 251. It is formed over the entire circumference of 260. The coating liquid distribution slit 262 communicates with the annular coating liquid distribution chamber 263. The coating liquid distribution chamber 263 is formed such that the coating liquid L in the storage tank 254 is supplied by the pressure feed pump 255 via the supply pipe 264.

  A slide surface 265 that is an inclined surface continuous with the coating liquid outlet 261 is formed below the coating liquid outlet 261 in FIG. 1A. A liquid reservoir (bead) 266 is formed below the inner edge of the slide surface 265 in FIG. 1A.

  In the circular slide hopper method, in the circular slide hopper coating apparatus, the coating liquid L is pushed out from the coating liquid distribution slit 262 and moved along the slide surface 265 while moving the substrate 251 in the direction of the arrow in FIGS. , Supplied to the substrate 251. The coating liquid L that has reached the inner edge of the slide surface 265 forms a bead between the inner edge of the slide surface 265 and the outer peripheral surface of the substrate 251, and is applied to the surface of the substrate 251. Thereby, the coating film F of the coating liquid L is formed on the substrate 251. The coating liquid that has not been used for forming the coating film F in the coating liquid L is discharged from the discharge port 267.

  In the coating liquid coating method using such a circular slide hopper coating apparatus, an appropriate gap (2 μm to 2 mm) exists between the inner edge portion of the slide surface 265 and the substrate 251. For this reason, the coating liquid can be applied without damaging the substrate 251. In addition, when forming the laminated structure, the coating liquid can be applied without damaging the layer formed on the substrate 251. Furthermore, even when forming a layered structure of components composed of components that can be dissolved in the same solvent, the circular slide hopper has a much shorter time in which the components are present in the solvent than the dip coating method, The coating liquid can be applied with almost no elution of components in the lower layer to the upper layer side.

  The solvent in the radically polymerizable composition includes a radical polymerizable monomer, a perfluoropolyether compound having a radical polymerizable functional group, insulating metal oxide particles having a radical polymerizable functional group, a charge transporting compound, , As long as it can be dissolved or dispersed. Examples of such solvents include methanol, ethanol, n-propyl alcohol, isopropyl alcohol, n-butanol, t-butanol, sec-butanol, benzyl alcohol, toluene, xylene, methyl ethyl ketone, cyclohexane, ethyl acetate, butyl acetate, methyl cellosolve. , Ethyl cellosolve, tetrahydrofuran, 1,3-dioxane, 1,3-dioxolane, pyridine and diethylamine.

  The radical polymerization initiator can be appropriately determined from known radical polymerization initiators according to the production process of the protective layer. Examples of the radical polymerization initiator include a photopolymerization initiator, a thermal polymerization initiator, and a polymerization initiator capable of initiating polymerization with both light and heat. The radical polymerization initiator is preferably a photopolymerization initiator, and is preferably an acyl phosphine oxide compound or an oxime ester compound, for example.

  Specific examples of the acylphosphine oxide compound include compounds represented by the following formulas P1 and P2.

  Specific examples of the oxime ester compound include compounds represented by the following formulas P3 and P4.

  It is preferable that content of the said polymerization initiator is 0.1-20 mass parts with respect to 100 mass parts of said radical polymerizable monomers, More preferably, it is 0.5-10 mass parts. One or more radical polymerization initiators may be used.

  The photopolymerization initiator may be used in combination with a photopolymerization accelerator having a photopolymerization promoting effect. Examples of the photopolymerization accelerator include triethanolamine, methyldiethanolamine, ethyl 4-dimethylaminobenzoate, isoamyl 4-dimethylaminobenzoate, (2-dimethylamino) ethyl benzoate and 4,4′-dimethylamino. Benzophenone is included.

  The radical scavenger has a polymerization inhibiting effect. With the radical scavenger, the crosslinking density of the radical polymerizable monomer in the protective layer can be adjusted. Thereby, it is possible to suppress the occurrence of image flow in the image forming process and to finely adjust the wear rate resulting from the cleaning of the protective layer. The radical scavenger may be appropriately selected from known compounds as long as the above function can be exhibited. The radical scavenger is preferably a compound represented by the following general formula (2) from the viewpoint of suppressing the occurrence of image flow without deteriorating transfer memory properties and cleaning properties.

In the general formula (2), R ₅ and R ₆ are each independently a linear alkyl group or branched alkyl group having 1 to 6 carbon atoms, and R ₇ is a hydrogen atom or a methyl group. is there.

  Specific examples of the radical scavenger represented by the general formula (2) include a compound represented by the following formula.

  The content of the radical scavenger can be appropriately adjusted as necessary within a range in which the above function can be exhibited. The amount is preferably 20 parts by mass or less, more preferably 10 parts by mass or less with respect to 100 parts by mass of the radical polymerizable monomer. One or more radical scavengers may be used.

The irradiation energy and irradiation time of actinic rays can be appropriately set according to the type of light source used, the output of the light source, the type of radical polymerizable monomer for forming the protective layer, and the like. Irradiation energy of active rays is preferably 5~500mJ / cm ^2, more preferably 5~10mJ / cm ^2. Moreover, it is preferable that irradiation time is 0.1 second-10 minutes, and it is more preferable that it is 0.1 second-5 minutes.

  Examples of types of actinic light sources include low pressure mercury lamps, medium pressure mercury lamps, ultra high pressure mercury lamps, carbon arc lamps, metal halide lamps, xenon lamps, flash (pulse) xenon, and ultraviolet LEDs. The output of the active light source is preferably 0.1 to 5 kW, and more preferably 0.5 to 3 kW. The wavelength of the actinic ray is preferably 250 to 400 nm (ultraviolet light).

  Through the above steps, the photoreceptor according to the present embodiment can be manufactured.

  The radical polymerizable monomer, the radical polymerizable PFPE, and the radical polymerizable insulating particles all have a radical polymerizable group function. Therefore, in the radical polymerizable composition, these components have high compatibility with each other. Therefore, both the radical polymerizable PFPE and the radical polymerizable insulating particles are uniformly dispersed in the radical polymerizable composition. As a result, the PFPE and the insulating metal oxide particles are uniformly dispersed in the protective layer and in both the surface direction and the thickness direction.

  In the protective layer, the radical polymerizable monomer, the radical polymerizable PFPE, and the radical polymerizable functional group of the radical polymerizable insulating particle react with each other to form a crosslinked structure. Therefore, even if the content of PFPE is large to some extent, a high-strength protective layer (organic-inorganic hybrid film) having sufficient wear resistance can be obtained.

  The protective layer maintains a high cleaning property over a long period of time. This is considered due to the following reasons. That is, in the protective layer, PFPE is present in a state of being bonded to the insulating metal oxide particles. For this reason, PFPE is likely to be dispersed throughout the protective layer. In this way, in the protective layer, PFPE and insulating metal oxide particles are dispersed in both the surface direction and the thickness direction of the protective layer, so that even if the protective layer is depleted on the surface of the protective layer, There is a sufficient amount of PFPE to maintain high cleanability (slidability).

  In addition, since the protective layer of the photoreceptor contains the insulating metal oxide particles, high film strength is obtained, and a decrease in electric field strength in the protective layer is suppressed. Thereby, in the said protective layer, content of the charge transport compound which can act as a plasticizer can be reduced. From such a viewpoint, the photoconductor according to the exemplary embodiment can achieve high wear resistance while ensuring a sufficient charge transport capability.

  Further, when the radically polymerizable PFPE has four or more radically polymerizable functional groups, the number of bonding points between the radically polymerizable monomer and the radically polymerizable insulating particles and the PFPE increases. From this point of view, the protective layer having high wear resistance and high cleaning properties can be obtained.

  The photoreceptor is used as an organic photoreceptor in an electrophotographic image forming apparatus. For example, the image forming apparatus includes the photosensitive member, a charging device for charging the surface of the photosensitive member, and an exposure for forming an electrostatic latent image by irradiating the charged surface of the photosensitive member with light. A developing device for supplying toner to the photosensitive member on which an electrostatic latent image is formed to form a toner image, and a transfer device for transferring the toner image on the surface of the photosensitive member to a recording medium And a fixing device for fixing the toner constituting the toner image transferred to the recording medium to the recording medium, and the toner image after the toner image is transferred to the recording medium in contact with a photoconductor And a cleaning device for removing transfer residual toner remaining on the surface of the photoreceptor.

  Further, the photoconductor supplies toner to the surface of the photoconductor on which the electrostatic latent image is formed, and forms a toner image corresponding to the electrostatic latent image on the surface of the photoconductor. The present invention is applied to an image forming method in which a toner is transferred from a surface of the photoreceptor to a recording medium and the toner remaining on the surface of the photoreceptor is removed by a cleaning device. The image forming method is performed by, for example, the image forming apparatus described above.

[Image forming apparatus]
FIG. 2 is a schematic diagram illustrating an example of a configuration of an image forming apparatus having the above-described photoconductor. As illustrated in FIG. 1, the image forming apparatus 100 includes an image reading unit 110, an image processing unit 30, an image forming unit 40, a paper transport unit 50, and a fixing device 60.

  The image forming unit 40 includes image forming units 41Y, 41M, 41C, and 41K that form images of toners of Y (yellow), M (magenta), C (cyan), and K (black). Since these have the same configuration except for the toner to be accommodated, the symbols representing the colors may be omitted hereinafter. The image forming unit 40 further includes an intermediate transfer unit 42 and a secondary transfer unit 43. These correspond to a transfer device.

  The image forming unit 41 includes an exposure device 411, a developing device 412, the above-described photoreceptor 413, a charging device 414, and a drum cleaning device 415. The charging device 414 is, for example, a corona charger. The charging device 414 may be a contact charging device in which a contact charging member such as a charging roller, a charging brush, or a charging blade is brought into contact with the photosensitive member 413 to be charged. The exposure device 411 includes, for example, a semiconductor laser as a light source and a light deflecting device (polygon motor) that irradiates the photoconductor 413 with laser light corresponding to an image to be formed.

  The developing device 412 is a two-component developing type developing device. The developing device 412 includes, for example, a developing container that contains a two-component developer, a developing roller (magnetic roller) that is rotatably disposed in an opening of the developing container, and a developing container that allows the two-component developer to communicate with each other. A partition partitioning the inside, a transport roller for transporting the two-component developer on the opening side of the developing container toward the developing roller, and an agitation roller for stirring the two-component developer in the developing container . For example, a two-component developer described later is accommodated in the developing container.

  The intermediate transfer unit 42 includes an intermediate transfer belt 421, a primary transfer roller 422 that presses the intermediate transfer belt 421 against the photoconductor 413, a plurality of support rollers 423 including a backup roller 423A, and a belt cleaning device 426. The intermediate transfer belt 421 is looped around the plurality of support rollers 423. When at least one drive roller of the plurality of support rollers 423 rotates, the intermediate transfer belt 421 travels at a constant speed in the arrow A direction.

  The secondary transfer unit 43 has a plurality of support rollers 431 including an endless secondary transfer belt 432 and a secondary transfer roller 431A. The secondary transfer belt 432 is stretched in a loop by the secondary transfer roller 431A and the support roller 431.

  The fixing device 60 fixes, for example, the fixing roller 62, the endless heating belt 20 that covers the outer peripheral surface of the fixing roller 62, and heats and melts the toner constituting the toner image on the paper S, and the paper S. A pressure roller 63 that presses the roller 62 and the heat generating belt 20. The paper S corresponds to a recording medium.

  The image reading unit 110 includes a paper feeding device 111 and a scanner 112. The paper transport unit 50 includes a paper feed unit 51, a paper discharge unit 52, and a transport path unit 53. In the three paper feed tray units 51a to 51c constituting the paper feed unit 51, paper S (standard paper, special paper) identified based on basis weight, size, etc. is stored for each preset type. . The conveyance path unit 53 includes a plurality of conveyance roller pairs such as registration roller pairs 53a.

  Next, image formation by the image forming apparatus 100 will be described.

  The scanner 112 optically scans and reads the document D on the contact glass. Reflected light from the document D is read by the CCD sensor 112a and becomes input image data. The input image data is subjected to predetermined image processing in the image processing unit 30 and sent to the exposure device 411.

  The photoconductor 413 rotates at a constant peripheral speed. The charging device 414 uniformly charges the surface of the photoreceptor 413 to a negative polarity. In the exposure apparatus 411, the polygon mirror of the polygon motor rotates at high speed, and laser light corresponding to the input image data of each color component is developed along the axial direction of the photoconductor 413, and the photoconductor 413 along the axial direction. Irradiated to the outer peripheral surface of. Thus, an electrostatic latent image is formed on the surface of the photoconductor 413.

  In the developing device 412, the toner particles are charged by stirring and transporting the two-component developer in the developing container, and the two-component developer is transported to the developing roller, and forms a magnetic brush on the surface of the developing roller. The charged toner particles are electrostatically attached from the magnetic brush to the portion of the electrostatic latent image on the photoreceptor 413. Thus, the electrostatic latent image on the surface of the photoconductor 413 is visualized, and a toner image corresponding to the electrostatic latent image is formed on the surface of the photoconductor 413. The “toner image” refers to a state where toner is gathered in an image form.

  The toner image on the surface of the photoreceptor 413 is transferred to the intermediate transfer belt 421 by the intermediate transfer unit 42. Transfer residual toner remaining on the surface of the photoconductor 413 after the transfer is removed by a drum cleaning device 415 having a drum cleaning blade that is in sliding contact with the surface of the photoconductor 413.

  When the intermediate transfer belt 421 is pressed against the photoconductor 413 by the primary transfer roller 422, a primary transfer nip is formed for each photoconductor by the photoconductor 413 and the intermediate transfer belt 421. In the primary transfer nip, the toner images of the respective colors are sequentially transferred onto the intermediate transfer belt 421.

  On the other hand, the secondary transfer roller 431A is pressed against the backup roller 423A via the intermediate transfer belt 421 and the secondary transfer belt 432. Accordingly, a secondary transfer nip is formed by the intermediate transfer belt 421 and the secondary transfer belt 432. The sheet S passes through the secondary transfer nip. The sheet S is conveyed to the secondary transfer nip by the sheet conveying unit 50. The correction of the inclination of the sheet S and the adjustment of the conveyance timing are performed by a registration roller unit provided with a registration roller pair 53a.

  When the sheet S is conveyed to the secondary transfer nip, a transfer bias is applied to the secondary transfer roller 431A. By applying the transfer bias, the toner image carried on the intermediate transfer belt 421 is transferred onto the paper S. The sheet S on which the toner image is transferred is conveyed toward the fixing device 60 by the secondary transfer belt 432.

  The fixing device 60 forms a fixing nip by the heat generating belt 20 and the pressure roller 63, and heats and presses the conveyed paper S at the fixing nip portion. Thus, the toner image is fixed on the paper S. The paper S on which the toner image has been fixed is discharged out of the apparatus by a paper discharge unit 52 having a paper discharge roller 52a.

  Note that transfer residual toner remaining on the surface of the intermediate transfer belt 421 after the secondary transfer is removed by a belt cleaning device 426 having a belt cleaning blade that is in sliding contact with the surface of the intermediate transfer belt 421.

  As described above, the image forming apparatus 100 can form an image.

  In the cleaning process of the image forming process, the cleaning blade is in sliding contact with the protective layer of the photoconductor 413 and removes transfer residual toner located on the surface of the protective layer. Normally, a protective layer composed of a polymerized cured film has a high frictional force against the cleaning blade, so-called blade torque, and therefore, during cleaning, the surface of the protective layer is applied by a lubricant application mechanism or a lubricant externally added to the toner. Lubricant is supplied. However, when an image with high coverage is printed, the lubricant on the surface of the protective layer is removed, and the blade torque is increased. As a result, uneven wear and scratches are likely to occur in the protective layer. If the charge transport compound is added to the protective layer from the viewpoint of suppressing the generation of the transfer memory and the perfluoropolyether compound is added to the protective layer from the viewpoint of reducing the blade torque, the film strength of the protective layer becomes insufficient. As a result, scratches on the protective layer in the cleaning process may be more likely to occur. If the scratches on the protective layer proceed too much, a phenomenon that the transfer residual toner on the surface of the protective layer cannot be removed properly, that is, so-called toner slippage may occur in the cleaning process.

  Therefore, in the photoreceptor 413 according to the present embodiment, the protective layer is made of a radical polymerizable composition containing a radical polymerizable monomer, a radical polymerizable PFPE, radical polymerizable insulating particles, and a charge transport compound. It consists of a polymerized and cured product by radical reaction. The radically polymerizable functional groups react with each other, and the constituent materials excluding the charge transport compound form a crosslinked structure. Thereby, although the protective layer of the photoreceptor 413 according to the present embodiment includes PFPE and the charge transport compound, it can ensure a sufficiently high film strength. That is, the protective layer of the photoconductor 413 according to the present embodiment has electrical characteristics (transfer memory suppression), abrasion resistance and scratch resistance, and high cleaning performance by PFPE (the suppression of the transfer memory). (Slidability) can both be achieved, and these characteristics can be expressed over a long period of time.

  In addition, the image forming apparatus 100 including the photoconductor 413 can stably form an image with a desired image quality over a long period of time.

  As is clear from the above description, the photoreceptor according to the present embodiment includes a conductive support, a photosensitive layer disposed on the conductive support, and a protection disposed on the photosensitive layer. A protective layer comprising a radically polymerizable monomer, a perfluoropolyether compound having a radically polymerizable functional group, and an insulating metal oxide having a radically polymerizable functional group. It is composed of a polymerized cured product obtained by radical reaction of a radically polymerizable composition containing particles and a charge transport compound. Therefore, in the above photoreceptor, blade torque can be reduced while ensuring sufficient film strength and charge transport capability, and these characteristics can be expressed over a long period of time.

  Therefore, the image forming apparatus having the photoconductor can form a high-quality image over a long period of time while suppressing the occurrence of image defects due to poor cleaning over a long period of time.

  It is more effective that the perfluoropolyether compound having a radical polymerizable functional group has four or more radical polymerizable functional groups from the viewpoints of wear resistance, scratch resistance and cleaning properties.

  It is even more effective that the radical polymerizable functional group is one or both of an acryloyl group and a methacryloyl group from the viewpoint that curing with a small amount of light or a short time is possible.

  The fact that the insulating metal oxide particles are silica particles suppresses the charging loss of the protective layer due to the charging of the insulating metal oxide particles and secures a sufficient electric field strength, while maintaining a sufficient electric field strength. From the viewpoint of reducing the content of, it is more effective.

  In the above embodiment, the photosensitive member having the intermediate layer has been described. However, the photosensitive member according to the present invention may not have the intermediate layer.

[Production of insulating particles]
(Preparation of insulating particles 1)
100 parts by mass of “silica (SiO ₂ ) particles” having a number average primary particle size of 20 nm as insulating metal oxide particles, 10 parts by mass of “Exemplary Compound S-15” and 1000 parts by mass of methyl ethyl ketone as a surface treatment agent. The mixture was placed in a wet sand mill (media: alumina beads having a diameter of 0.5 mm) and mixed at 30 ° C. for 6 hours. Thereafter, methyl ethyl ketone and alumina beads were separated from the silica particles by filtration, and the silica particles were dried at 60 ° C. Thus, insulating particles 1 which are the radical polymerizable insulating particles were produced.

(Preparation of insulating particles 2)
As shown in Table 1, as insulating metal oxide particles, silica (SiO ₂ ) particles having a number average primary particle size of 12 nm were used, and as a surface treating agent, Exemplified Compound S-7 was used as an insulating material. Insulating particles 2 as the radical polymerizable insulating particles were prepared in the same manner as the preparation of the particles 1.

(Preparation of insulating particles 3)
As shown in Table 1, the radical polymerizability is the same as the production of the insulating particles 1 except that silica (SiO ₂ ) particles having a number average primary particle size of 30 nm are used as the insulating metal oxide particles. Insulating particles 3 which are insulating particles were produced.

(Preparation of insulating particles 4)
As shown in Table 1, the radical polymerizability is the same as the production of the insulating particles 2 except that silica (SiO ₂ ) particles having a number average primary particle size of 30 nm are used as the insulating metal oxide particles. Insulating particles 4 which are insulating particles were produced.

(Preparation of insulating particles 5)
As shown in Table 1, the radical polymerizable property is the same as that of the insulating particle 1 except that silica (SiO ₂ ) particles having a number average primary particle size of 50 nm are used as the insulating metal oxide particles. Insulating particles 5 which are insulating particles were produced.

(Preparation of insulating particles 6)
As shown in Table 1, the radicals described above were produced in the same manner as in the production of the insulating particles 1 except that alumina (Al ₂ O ₃ ) particles having a number average primary particle size of 50 nm were used as the insulating metal oxide particles. Insulating particles 6 which are polymerizable insulating particles were produced.

(Preparation of insulating particles 7)
As shown in Table 1, insulating particles 7 were prepared in the same manner as the insulating particles 3 except that the surface treatment of the insulating metal oxide particles was not performed.

  For each insulating particle, the insulating particle No. Table 1 shows the type of insulating metal oxide particles (IMOP), the type of surface treatment agent, and the number average primary particle size (D) of insulating particles (insulating metal oxide particles).

[Production of photoconductor]
(Preparation of photoreceptor 1)
(1) Preparation of conductive support The surface of a cylindrical aluminum support having a diameter of 100 mm was cut to prepare a conductive support.

(2) Formation of intermediate layer The following components were mixed in the following amounts, and a sand mill was used as a disperser to perform batch-type dispersion for 10 hours to prepare an intermediate layer forming coating solution.
Polyamide resin 10 parts by mass Titanium oxide particles 11 parts by mass Ethanol 200 parts by mass

  As the polyamide resin (binder resin), X1010 (manufactured by Daicel Degussa Co., Ltd.) was used, and as the titanium oxide particles (metal oxide particles), SMT500SAS (manufactured by Teika Corporation) was used.

  Next, a coating solution for forming an intermediate layer was applied to the surface of the conductive support by a dip coating method and dried at 110 ° C. for 20 minutes to form an intermediate layer having a thickness of 2 μm on the conductive support.

(3) Formation of charge generation layer The following components are mixed in the following amounts, and a circulating flow rate of 40 L / H at 19.5 kHz and 600 W using a circulating ultrasonic homogenizer (RUS-600TCVP; manufactured by Nippon Seiki Seisakusho Co., Ltd.) The coating solution for forming the charge generation layer was prepared by dispersing for 0.5 hour.
Charge generation compound 24 parts by weight Polyvinyl butyral 12 parts by weight Solvent 400 parts by weight

  Examples of the charge generation compound include titanyl phthalocyanine having clear peaks at 8.3 °, 24.7 °, 25.1 °, and 26.5 ° by Cu-Kα characteristic X-ray diffraction spectrum measurement, and (2R, 3R)- A mixed crystal of 1: 1 adduct of 2,3-butanediol and non-added titanyl phthalocyanine was used, and as polyvinyl butyral (binder resin), S-REC BL-1 (Sekisui Chemical Co., Ltd. “Registered trademark of the company” was used, and 3-methyl-2-butanone / cyclohexanone = 4/1 (V / V) was used as the solvent.

  Next, a charge generation layer forming coating solution was applied to the surface of the intermediate layer by a dip coating method and dried to form a charge generation layer having a thickness of 0.3 μm on the intermediate layer.

(4) Formation of charge transport layer A coating solution for forming a charge transport layer was prepared by mixing and dissolving the following components in the following amounts.
Charge transport compound (Exemplified Compound T16) 60 parts by weight Polycarbonate resin 100 parts by weight Antioxidant 4 parts by weight

  Z300 (manufactured by Mitsubishi Gas Chemical Co., Inc.) was used as the polycarbonate resin (binder resin), and IRGANOX 1010 (manufactured by BASF, “IRGANOX” is a registered trademark of the company) was used as the antioxidant.

  Next, a charge transport layer forming coating solution was applied to the surface of the charge generation layer by a dip coating method, and dried at 120 ° C. for 70 minutes to form a charge transport layer having a thickness of 24 μm on the charge generation layer. .

(5) Formation of Protective Layer A protective layer-forming coating solution (radical polymerizable composition) was prepared by mixing and dissolving the following components in the following amounts. In addition, Irgacure 819 (made by BASF Japan) was used as a polymerization initiator.
Radical polymerizable monomer (Exemplary compound M1) 100 parts by mass Radical polymerizable PFPE (Exemplary compound P-2M) 7 parts by mass Insulating particles 1 33 parts by mass Charge transport compound (Exemplary compound T16) 33 parts by mass Polymerization initiator 10 parts by mass 2-butanol 320 parts by mass Tetrahydrofuran (THF) 80 parts by mass

  Subsequently, the coating solution for forming the radical polymerizable composition was formed by applying the coating liquid for forming the protective layer onto the surface of the charge transport layer using a circular slide hopper coating apparatus. Next, the coating film was cured by irradiating the coating film with ultraviolet rays from a metal halide lamp for 1 minute to form a protective layer having a dry film thickness of 3.0 μm on the charge transport layer. In this way, the photoreceptor 1 was produced.

(Production of photoconductors 2 to 7, C1 and C2)
As shown in Tables 2 and 3, the type and content of insulating particles, the type and content of radical polymerizable PFPE, the type of charge transport compound, the content of radical scavenger, and the content of polymerization initiator Photoconductors 2 to 7, C1 and C2 were respectively produced in the same manner as in the production of the photoconductor 1 except that was changed.

As a radical scavenger, a Sumilizer GS (a compound in which R ⁵ and R ⁶ are tert-pentyl groups and R ⁷ is a methyl group in the above general formula (2), manufactured by Sumitomo Chemical Co., Ltd., “Smilizer” The compounds represented by the following formulas T65 and T66 were further used as charge transport compounds.

For each photoreceptor, category, photoreceptor No. , Radical polymerizable monomer type, insulating particle type and content, radical polymerizable PFPE type and content, charge transport compound type and content, radical scavenger content, and polymerization initiator content Are shown in Table 2 and Table 3. In Tables 2 and 3, “monomer” indicates a radical polymerizable monomer, and “r-PFPE” indicates a radical polymerizable PFPE. In Table 2, the content of each component is shown in parts by mass, and in Table 3, the content of each component is shown in volume%. When converting from mass parts to volume%, the total of components excluding the solvent in the radical polymerizable composition is calculated as 100%, the specific gravity of silica is 2.2 g / cm ³ , and the specific gravity of alumina is 3.9 g / cm ³ , the specific gravity of r-PFPE is 1.5 g / cm ³ , the specific gravity of the charge transport compound is 1.1 g / cm ³ , the specific gravity of the radical scavenger is 1.1 g / cm ³ , and the specific gravity of the polymerization initiator is 1. Calculation was performed as 1 g / cm ³ .

[Evaluation]
Each of the photoreceptors 1 to 7, C1 and C2 was mounted on a full-color copying machine (bizhub PRO C554: manufactured by Konica Minolta Business Technologies, Inc., “bizhub” is a registered trademark of the company). First, an endurance test was performed in which 300,000 A4-size character images with an image ratio of 20% were continuously printed on both sides of A4-size neutral paper by lateral feeding. Next, the following evaluations (transfer memory, abrasion resistance, image flow, and toner slipping) were performed.

(1) Transfer memory It was set so that a solid image was formed at the first rotation of the photoconductor and a halftone image was formed at the second rotation of the photoconductor in an environment of 30 ° C. and 80% RH before and after the durability test. The image was printed on A3 size POD gloss coated paper (100 g / m ² ; manufactured by Oji Paper Co., Ltd.). Then, it was confirmed whether or not the pattern of the solid image appears as a transfer memory in the halftone image. Specifically, a difference (ΔID) between a reflection density of a region corresponding to the solid image in the halftone image and a reflection density of a region not corresponding to the solid image in the halftone image is calculated. Based on the evaluation criteria, the transfer memory of each photoconductor was evaluated. In addition, about the said reflection density, it measured using the Macbeth reflection densitometer (RD-918; Gretag Macbeth company make). A case where the evaluation results were “◎” and “。” was determined to be acceptable.
(Evaluation criteria)
◎: ΔID is 0.05 or less ○: ΔID is larger than 0.05 and 0.10 or less ×: ΔID is larger than 0.10

(2) Abrasion resistance An eddy current type film of a uniform film thickness portion of the photoconductor before and after the endurance test (excluding portions where the film thickness at both ends of the photoconductor is nonuniform is excluded based on the film thickness distribution profile) Ten thicknesses were measured randomly using a thickness measuring instrument (trade name: “EDDY560C”, manufactured by HELMUT FISCHER GMBTE CO), and the average value was calculated to obtain the film thickness of the photoreceptor. The difference in film thickness between the photoreceptors before and after the durability test was defined as the amount of wear. The amount of wear per 100 krot (100,000 revolutions) was defined as an α value, and the wear resistance of each photoconductor was evaluated based on the following criteria. A case where the evaluation results were “◎” and “。” was determined to be acceptable.
(Evaluation criteria)
A: α value is 0.1 or more and less than 0.3 ○: α value is 0.3 or more and less than 0.5 ×: α value is 0.5 or more

(3) Image flow In an environment of 30 ° C. and 80% RH, the A4 plate character image with an image ratio of 6% is printed on the A4 plate neutral paper by 1000 sheets. The main power was turned on 12 hours after the main power was turned off. Next, immediately after the print was ready, a halftone image (relative reflection density of 0.4 with a Macbeth densitometer) and a 6 dot lattice image were printed on the entire surface of the A3 neutral paper. The printed halftone image and the lattice image were visually observed, and the presence or absence of image flow was evaluated for each photoconductor based on the following criteria. A case where the evaluation results were “◎” and “。” was determined to be acceptable.
(Evaluation criteria)
A: There is no occurrence of density unevenness in the halftone image, and there is no defect or thinning of the line width in the lattice image.
A: A band-shaped density reduction region along the long axis direction of the photoconductor is observed in the halftone image, but there are no defects and no line width narrowing in the lattice image.
X: Defects or thin line widths are observed in the lattice image.

(4) Toner slip-through In an environment of 10 ° C. and 15% RH, a halftone image with a coverage rate of 80% is recorded in A3 so that the black background portion is located in the front portion and the white background portion is located in the rear portion in the paper transport direction. 20,000 sheets were printed on the plate neutral paper, and the white background portion of the 20,000th paper was visually observed, and toner slipping was evaluated based on the following criteria. A case where the evaluation results were “◎” and “。” was determined to be acceptable.
(Evaluation criteria)
◎: No stain was observed on the white background ○: A slight streak-like stain occurred on the white background, but there was no practical problem ×: An obvious streak-like stain occurred on the white background, which was practical Have a problem

  For each photoreceptor, category, photoreceptor No. Table 4 shows the evaluation results.

  As shown in Table 4, with respect to the photoconductors 1 to 7, it was possible to suppress the generation of the transfer memory and the image flow while ensuring sufficient wear resistance and cleaning properties (through toner). This is because the protective layer is composed of a polymerized cured product by radical reaction of a radically polymerizable composition containing a radically polymerizable monomer, a radically polymerizable PFPE, radically polymerizable insulating particles, and a charge transporting compound. It is thought that it is because.

  Further, in the photoconductor 6, the generation of the transfer memory was further suppressed as compared with the photoconductor 7. This is because the relative dielectric constant of the silica particles contained in the protective layer of the photoconductor 6 is lower than that of the alumina particles contained in the protective layer of the photoconductor 7, so that the electric field of the protective layer due to the charging of the insulating particles. This is probably because the loss was further suppressed.

  On the other hand, as shown in Table 4, with respect to the photoreceptor C1, cleaning properties (toner slipping) were insufficient. This is presumably because, for the photoreceptor C1, the protective layer is composed of a polymerized cured product obtained by radical reaction of a radically polymerizable composition not containing radically polymerizable PFPE. Further, as shown in Table 4, the photoreceptor C2 had insufficient wear resistance. This is presumably because the photoreceptor C2 is composed of a polymerized cured product by radical reaction of a radically polymerizable composition containing insulating metal oxide particles having no radically polymerizable functional group.

  According to the present invention, in the electrophotographic photosensitive member of the electrophotographic image forming apparatus, it is possible to achieve both electrical characteristics, abrasion resistance, scratch resistance, and cleaning properties, and to exhibit such characteristics over a long period of time. Can be made. Therefore, according to the present invention, it is expected that the electrophotographic image forming apparatus is further enhanced in durability and further spread.

20 Heat generating belt 30 Image processing unit 40 Image forming unit 41Y, 41M, 41C, 41K Image forming unit 42 Intermediate transfer unit 43 Secondary transfer unit 50 Paper transport unit 51 Paper feed unit 51a, 51b, 51c Paper feed tray unit 52 Paper discharge Section 52a Discharge roller 53 Conveyance path section 53a Registration roller pair 60 Fixing apparatus 62 Fixing roller 63 Pressure roller 100 Image forming apparatus 110 Image reading section 111 Paper feeding apparatus 112 Scanner 112a CCD sensor 251 Base material 254 Storage tank 255 Pressure feed pump 260 Coating head 261 Coating liquid outlet 262 Coating liquid distribution slit 263 Coating liquid distribution chamber 264 Supply pipe 265 Slide surface 266 Liquid reservoir 267 Discharge port L Coating liquid F Coating film 411 Exposure device 412 Developing device 413 Photoconductor 41 A charging device 415 the drum cleaning device 421 intermediate transfer belt 422 primary transfer roller 423,431 support rollers 423A backup roller 426 belt cleaning device 431A secondary transfer roller 432 Secondary transfer belt D document S Paper

Claims (6)

An electrophotographic photosensitive member comprising a conductive support, a photosensitive layer disposed on the conductive support, and a protective layer disposed on the photosensitive layer,
The protective layer includes a radical polymerizable monomer, a perfluoropolyether compound having a radical polymerizable functional group, insulating metal oxide particles having a radical polymerizable functional group, and a charge transport compound. It consists of a polymerized and cured product by radical reaction of the composition,
Electrophotographic photoreceptor.   The electrophotographic photoreceptor according to claim 1, wherein the perfluoropolyether compound having a radical polymerizable functional group has four or more radical polymerizable functional groups.   The electrophotographic photosensitive member according to claim 1, wherein the radical polymerizable functional group is one or both of an acryloyl group and a methacryloyl group.   The electrophotographic photosensitive member according to claim 1, wherein the insulating metal oxide particles are silica particles. An electrophotographic image forming apparatus comprising: an electrophotographic photosensitive member; and a cleaning device that contacts the electrophotographic photosensitive member and removes transfer residual toner on the electrophotographic photosensitive member,
The electrophotographic photoreceptor is the electrophotographic photoreceptor according to any one of claims 1 to 4.
Image forming apparatus. A step of applying a radical polymerizable composition containing a radical polymerizable monomer on the photosensitive layer, forming a coating film of the radical polymerizable composition on the photosensitive layer, and irradiating the coating film with actinic rays A step of polymerizing the radical polymerizable monomer to form a protective layer, and a method for producing an electrophotographic photoreceptor,
The radical polymerizable composition includes a radical polymerizable monomer, a perfluoropolyether compound having a radical polymerizable functional group, insulating metal oxide particles having a radical polymerizable functional group, and a charge transport compound. Using a radically polymerizable composition,
A method for producing an electrophotographic photoreceptor.

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