Electrophotographic photoreceptor, electrophotographic apparatus, process cartridge, and method for manufacturing an electrophotographic photoreceptor

Abstract

To provide an electrophotographic photoreceptor which comprises a surface layer that features superior dispersibility of fluorine atom-containing resin particles and suppresses electric potential variations associated with repetitive use.SOLUTION: An electrophotographic photoreceptor is provided, comprising a surface layer containing fluorine atom-containing resin particles, a binding material, and a polymer A having a specific structural unit.SELECTED DRAWING: Figure 1

Description

[Technical Field]

[0001] This disclosure relates to an electrophotographic photoreceptor, a process cartridge having the electrophotographic photoreceptor, an electrophotographic apparatus, and a method for manufacturing an electrophotographic photoreceptor. [Background technology]

[0002] Electrophotographic photoreceptors containing organic photoconductive materials (charge-generating materials) are widely used in electrophotographic devices. In recent years, there has been a demand for improved mechanical durability (wear resistance) of electrophotographic photoreceptors in order to extend their lifespan and improve image quality during repeated use.

[0003] One technique for improving the wear resistance of electrophotographic photoreceptors is to incorporate fluorine atom-containing resin particles into the surface layer of the electrophotographic photoreceptor, thereby reducing friction between the surface layer and contact members such as cleaning blades. Patent Document 1 discloses a technique for forming a surface layer using a dispersion of fluorine atom-containing resin particles, such as polytetrafluoroethylene resin particles, as a coating liquid for the surface layer.

[0004] Furthermore, when preparing a dispersion of fluorine atom-containing resin particles, a method is known in which a fluorine atom-containing (meth)acrylic polymer is used as a dispersant for the fluorine atom-containing resin particles in order to improve dispersibility. Patent Document 2 discloses a technique for improving the dispersibility of fluorine atom-containing resin particles by using a fluorine atom-containing (meth)acrylic polymer of a specific structure as a dispersant.

[0005] Patent Document 3 discloses a technique for improving the wear resistance of the surface layer of an electrophotographic photoreceptor by incorporating a crosslinked material of a guanamine compound or melamine compound with a charge transport material into the surface layer.

[0006] Patent Document 4 discloses an electrophotographic photoreceptor having a surface layer containing a fluorine-based graft polymer and fluorine atom-containing resin particles, wherein the fluorine-based graft polymer contains structural units having acidic groups with a pKa of 3 or less. [Prior art documents] [Patent Documents]

[0007] [Patent Document 1] Japanese Patent Application Publication No. 06-332219 [Patent Document 2] Japanese Patent Publication No. 2009-104145 [Patent Document 3] Japanese Patent Publication No. 2012-203253 [Patent Document 4] Japanese Patent Publication No. 2021-47236 [Overview of the project] [Problems that the invention aims to solve]

[0008] As a result of our investigations, we found that there is room for further improvement in the technologies disclosed in Patent Documents 2 and 3, specifically in terms of suppressing potential fluctuations during repeated use without impairing the dispersibility of fluorine atom-containing resin particles.

[0009] One aspect of this disclosure aims to provide an electrophotographic photoreceptor that suppresses image defects due to poor dispersion of fluorine atom-containing resin particles and suppresses potential fluctuations during repeated use in high-temperature and high-humidity environments.

[0010] Another aspect of this disclosure relates to a process cartridge equipped with the electrophotographic photoreceptor, and an electrophotographic apparatus equipped with the process cartridge. Another aspect of this disclosure is toward providing a method for manufacturing the electrophotographic photoreceptor. [Means for solving the problem]

[0011] According to one aspect of the present disclosure, in an electrophotographic photoreceptor having a surface layer, the surface layer comprises fluorine atom-containing resin particles, a binder material, and structural units represented by the following formula (1). , and structural units represented by the following formula (2) A polymer A having and Rf in formula (1)1 and Rf 2 There is provided an electrophotographic photoreceptor characterized in that the total number of carbon atoms of the following is 6 or more.

Chemical formula

Chemical formula

Chemical formula

[0013] Also, according to another aspect of the present disclosure, there is provided a process cartridge that integrally supports the electrophotographic photoreceptor and at least one means selected from the group consisting of charging means, developing means, transferring means, discharging means, and cleaning means, and is detachable from the electrophotographic apparatus main body. Furthermore, according to other aspects of this disclosure, an electrophotographic apparatus is provided having the electrophotographic photoreceptor, as well as a charging means, an exposure means, a developing means, and a transfer means. Furthermore, according to other aspects of this disclosure, a method for manufacturing the electrophotographic photoreceptor is provided. [Effects of the Invention]

[0014] According to one aspect of this disclosure, an electrophotographic photoreceptor can be provided that exhibits excellent dispersibility of fluorine atom-containing resin particles in the surface layer and suppresses potential fluctuations during repeated use in high-temperature and high-humidity environments. [Brief explanation of the drawing]

[0015] [Figure 1] This is a schematic diagram showing an example of the configuration of an electrophotographic photoreceptor in this disclosure. [Figure 2] This figure shows an example of a polishing machine using abrasive sheets. [Figure 3] This is a schematic diagram showing an example of a process cartridge having an electrophotographic photoreceptor according to the present disclosure. [Figure 4] This is a schematic diagram showing an example of an electrophotographic apparatus having the electrophotographic photoreceptor of this disclosure. [Modes for carrying out the invention]

[0016] The present disclosure will be described in detail below with reference to preferred embodiments. As a result of our investigations, we have found that the surface layer of an electrophotographic photoreceptor contains fluorine atom-containing resin particles, a binder material, and structural units represented by the following formula (1). , and structural units represented by the following formula (2) A polymer A having Rf 1 and Rf 2 We found that by setting the total number of carbon atoms to 6 or more, an electrophotographic photoreceptor can be obtained that exhibits excellent dispersibility of fluorine atom-containing resin particles in the surface layer and suppresses potential fluctuations during repeated use in high-temperature, high-humidity environments. [ka] In formula (1), R 11R represents a hydrogen atom or a methyl group. 12 This represents either a single bond, a methylene group, or an ethylene group. Rf 1 This represents a perfluoroalkylene group having 1 to 5 carbon atoms, or a perfluoroalkylidene group having 1 to 5 carbon atoms. Rf 2 This represents a perfluoroalkyl group having 1 to 5 carbon atoms. [ka] (In formula (2), Y A1 This shows an unsubstituted alkylene group, Y B This represents an unsubstituted alkylene group, a halogen-substituted alkylene group, a hydroxyl-substituted alkylene group, an ester bond (-COO-), an amide bond (-NHCO-), or a urethane bond (-NHCOO-), or a divalent linking group that can be derived by combining one or more of these groups and bonds with -O- or -S-, or a single bond. Z A This refers to the structure represented by the following formula (2A), a cyano group, or a phenyl group. R 21 , and R 22 This represents a hydrogen atom or a methyl group. m is an integer between 25 and 150 (inclusive). [ka] (In formula (2A), Z A1 This represents an alkyl group having 1 to 4 carbon atoms.

[0017] The polymer A may or may not have structural units having acidic groups with a pKa of 3 or less, but it is preferable that it does not have such units.

[0018] The surface layer may or may not contain a polymer having structural units represented by formula (1) and structural units having acidic groups with a pKa of 3 or less, but it is preferable that it does not contain such polymers.

[0019] The pKa of an acidic group is determined by measurement using known methods such as titration. Examples of acidic groups with a pKa of 3 or less include sulfonic acid groups (methanesulfonic acid: pKa-2.6), phosphonic acid groups (first dissociation: pKa1.5), phosphate groups (first dissociation: pKa2.12), and alkyl fluoride carboxylic acid groups (e.g., trifluoroacetic acid: pKa-0.25, difluoroacetic acid: pKa1.24, monofluoroacetic acid: pKa2.66).

[0020] Here, the inventors believe that polymer A having the structural unit shown in formula (1) acts as a dispersant for fluorine atom-containing resin particles in the process of preparing a coating solution for the surface layer of an electrophotographic photoreceptor.

[0021] The inventors speculate that the electrophotographic photoreceptor of this disclosure exhibits excellent dispersibility of fluorine atom-containing resin particles in the surface layer and excellent suppression of potential fluctuations during repeated use in high-temperature and high-humidity environments as follows.

[0022] Electrophotographic photoreceptors having a surface layer containing fluorine atom-containing resin particles and a dispersant tend to exhibit large potential fluctuations during repeated use, particularly under high-temperature and high-humidity environments. This is due to the dispersant adhering to the fluorine atom-containing resin particles contained in the surface layer, which has a (CF2) property. n -This is thought to be because electric charge tends to accumulate in the chain.

[0023] Based on the inventors' investigations, -(CF2) n -When incorporating a polymer having structural units including chains into the surface layer, -(CF2) n -Chains- (CF2) n -We found that the presence of oxygen atoms between the chain and the oxygen atom has the effect of suppressing charge trapping. However, -(CF2) n - The more carbon atoms in the chain, the easier it is for charge to accumulate, and in some cases, the effect of suppressing potential fluctuations may not be sufficiently obtained.

[0024] As a result of further investigation by the present inventors, it was found that by incorporating polymer A having the structural unit shown in formula (1) into the surface layer, charge trapping is suppressed, and an electrophotographic photoreceptor can be obtained in which potential fluctuations during repeated use are suppressed even in high-temperature and high-humidity environments.

[0025] Rf in equation (1) above 1 and Rf 2 By using a perfluoroalkylene group having 1 to 5 carbon atoms or a perfluoroalkylidene group having 1 to 5 carbon atoms, it is thought that the accumulation of charge in the structural unit represented by formula (1) can be suppressed. Also, R in formula (1) 12 By using a single bond, a methylene group, or an ethylene group, the difference in surface energy between the structural unit represented by formula (1) and the fluorine atom-containing resin particles is reduced, making it easier for the fluorine atom-containing resin particles to adhere to each other.

[0026] <Fluorine atom-containing resin particles> The surface layer of the electrophotographic photoreceptor of this disclosure contains fluorine atom-containing resin particles.

[0027] When the photosensitive layer of an electrophotographic photoreceptor is a multilayer photosensitive layer and the protective layer is the surface layer, the content of fluorine atom-containing resin particles is 5% by mass or more and 40% by mass or less relative to the protective layer.

[0028] Examples of resins contained in the fluorine atom-containing resin particles used in this disclosure include: polytetrafluoroethylene resin, polychlorotrifluoroethylene resin, polytetrafluoroethylene propylene resin, polyvinyl fluoride resin, polyvinylidene fluoride resin, or polydichlorodifluoroethylene resin. It is also preferable to use particles containing multiple types of the above resins. Among the above, from the viewpoint of improving dispersibility, polytetrafluoroethylene resin is more preferable for the fluorine atom-containing resin particles.

[0029] In cross-sectional observation of the surface layer, it is preferable that the arithmetic mean of the major axis of the primary particles (average primary particle size) measured from the secondary electron image obtained by scanning electron microscopy is between 150 nm and 300 nm, from the viewpoint of improving dispersibility and suppressing potential fluctuations. Furthermore, it is preferable that the average primary particle size of the fluorine atom-containing resin particles is between 180 nm and 250 nm.

[0030] It is preferable that the fluorine atom-containing resin particles have an average roundness (average roundness) of 0.75 or higher, calculated from the area and circumference of primary particles measured from secondary electron images obtained by scanning electron microscopy.

[0031] To bring the measured values ​​of the average primary particle size and average roundness of the fluorine atom-containing resin particles contained in the surface layer of the electrophotographic photoreceptor of this disclosure within the above range, fluorine atom-containing resin particles can be used such that the average primary particle size and average roundness values ​​measured and calculated by the following method fall within the above range.

[0032] (Measurement method for average primary particle size and average roundness) In other words, in the embodiments of this disclosure, the average particle size and average roundness of the fluorine atom-containing resin particles to be incorporated into the surface layer of the electrophotographic photoreceptor were measured using a field emission scanning electron microscope (FE-SEM) as follows. Fluorine atom-containing resin particles were attached to a commercially available carbon conductive tape, and fluorine atom-containing resin particles not attached to the conductive tape were removed with compressed air, followed by platinum deposition. The deposited fluorine atom-containing resin particles were observed using a Hitachi High-Technologies Corporation FE-SEM (S-4700). The measurement conditions for the FE-SEM were as follows. Acceleration voltage: 2kV WD: 5mm Magnification: 20,000 times Pixel count: 1280 pixels vertically, 960 pixels horizontally (size of each pixel: 5nm) The Ferret diameter of 100 particles was determined from the obtained images using ImageJ (open-source software from the National Institutes of Health (NIH)), and the average value was calculated to determine the average particle size. Similarly, the area and perimeter were determined, the roundness was calculated using the following formula (II), and the average value was calculated and defined as the average roundness. Roundness = 4 × π × (area) ÷ (perimeter squared) Equation (II)

[0033] The fluorine atom-containing resin particles of this disclosure may be used alone or in combination of two or more types.

[0034] <Polymer A having the structural unit shown in formula (1)> The surface layer of the electrophotographic photoreceptor of this disclosure contains polymer A having a structural unit represented by the following formula (1). [ka] In formula (1), R 11 R represents a hydrogen atom or a methyl group. 12 Rf represents a single bond, a methylene group, or an ethylene group. 1 This represents a perfluoroalkylene group having 1 to 5 carbon atoms, or a perfluoroalkylidene group having 1 to 5 carbon atoms. Rf 2 This represents a perfluoroalkyl group having 1 to 5 carbon atoms.

[0035] In equation (1) above, R 11 R is a hydrogen atom or a methyl group, 12 R is a single bond, a methylene group, or an ethylene group. 12 When Rf is changed to an alkylene having 3 or more carbon atoms, the surface energy difference between the structural unit shown in formula (1) and the fluorine atom-containing resin particles becomes large, making it difficult for the fluorine atom-containing resin particles to adhere sufficiently, and resulting in insufficient dispersibility. In formula (1), Rf 1 This is a perfluoroalkylene group having 1 to 5 carbon atoms, or a perfluoroalkylidene group having 1 to 5 carbon atoms, and Rf 2 Rf is a perfluoroalkyl group having 1 to 5 carbon atoms. 1 and Rf 2If the number of carbon atoms is increased to 6 or more, the accumulation of charge in the structural unit shown in formula (1) cannot be sufficiently suppressed, and potential fluctuations cannot be sufficiently suppressed when the electrophotographic photoreceptor is repeatedly used.

[0036] Furthermore, in formula (1) above, Rf 1 and Rf 2 The total number of carbon atoms is preferably 6 or more and 9 or less, from the viewpoint of improving the dispersibility of the fluorine atom-containing resin particles. Furthermore, from the viewpoint of suppressing potential fluctuations, Rf 1 and Rf 2 The total number of carbon atoms is more preferably 6 or more and 8 or less.

[0037] Examples of structural units represented by formula (1) used in this disclosure include those shown in Table 1 below.

[0038] [Table 1]

[0039] Of the polymer A contained in the surface layer of the electrophotographic photoreceptor of this disclosure, the structural unit represented by formula (1) is preferably 5% to 95% of the total structural units of polymer A, from the viewpoint of improving the dispersibility of fluorine atom-containing resin particles. Furthermore, the structural unit represented by formula (1) is more preferably 50% to 95% of the total structural units of polymer A, and even more preferably 70% to 90% of the total structural units of polymer A.

[0040] Furthermore, of the polymer A contained in the surface layer of the electrophotographic photoreceptor of this disclosure, the structural unit represented by formula (1) is preferably 0.1% by mass or more and 80% by mass or less of the total structural units of polymer A, from the viewpoint of improving the dispersibility of fluorine atom-containing resin particles. Moreover, in the polymer A, the composition ratio of the structural unit represented by formula (1) is more preferably 1% by weight or more and 80% by weight or less of the total number of structural units constituting polymer A, from the viewpoint of improving the uniformity of dispersion, and even more preferably 4% by weight or more and 66% by weight or less.

[0041] The polymer A further comprises structural units represented by the following formula (2). ru. [ka] [ka] In formula (2), Y A1 This shows an unsubstituted alkylene group, Y B This represents an unsubstituted alkylene group, a halogen-substituted alkylene group, a hydroxyl-substituted alkylene group, an ester bond (-COO-), an amide bond (-NHCO-), or a urethane bond (-NHCOO-), or a divalent linking group that can be derived by combining one or more of these groups and bonds with -O- or -S-, or a single bond. Z A This represents the structure represented by the above formula (2A), a cyano group, or a phenyl group. R 21 , and R 22 This represents a hydrogen atom or a methyl group. m is an integer between 25 and 150 (inclusive). In formula (2A), Z A1 This represents an alkyl group having 1 to 4 carbon atoms.

[0042] In formula (2), Y B If it shows an ester bond, -Y A1 -YB -CH2- is -Y A1 -CO-O-CH2- and -Y A1 Either -O-CO-CH2- is acceptable, preferably -Y A1 It is -CO-O-CH2-. Also, in equation (2), Y B If it shows an amide bond, -Y A1 -Y B -CH2- is -Y A1 -NH-CO-CH2- and -Y A1 Either -CO-NH-CH2- is acceptable, preferably -Y A1 It is -NH-CO-CH2-. Also, in equation (2), Y B If it is a urethane bond, -Y A1 -Y B -CH2- is -Y A1 -NH-CO-O-CH2- and -Y A1 Either -O-CO-NH-CH2- is acceptable, preferably -Y A1 It is -NH-CO-O-CH2-.

[0043] In equation (2) above, -Y A1 -Y B -but, -Y A1 -(Y A2 ) b -(Y A3 ) c -(Y A4 ) d -(Y A5 ) e -(Y A6 ) f - The structure shown is preferable. Here, Y A1 This shows an unsubstituted alkylene group, Y A2 This represents a methylene group substituted with at least one selected from the group consisting of hydroxyl groups and halogen atoms. Y A3 This shows an unsubstituted alkylene group, Y A4 These represent ester bonds, amide bonds, or urethane bonds. Y A5represents an unsubstituted alkylene group, Y A6 represents an oxygen atom or a sulfur atom, b, c, d, e, and f each independently represent 0 or 1.

[0044] It is preferable that the polymer A has only the structural unit represented by the above formula (1) and the structural unit represented by the above formula (2) as structural units. In the above formula (2),

Chemical formula

Chemical formula

[0045] Examples of the structural unit represented by the above formula (2) include the structures shown in Table 2.

Table 2-1

Table 2-2

[0046] In the polymer A, the ratio of the content of the structural unit represented by the above formula (1) to the content of the structural unit represented by the above formula (2), the content of the structural unit represented by the above formula (1): the content of the structural unit represented by the above formula (2), is preferably 1:19 to 19:1 in molar ratio. More preferably, it is 1:1 to 19:1 in molar ratio, and even more preferably, it is 7:3 to 9:1 in molar ratio.

[0047] The weight-average molecular weight of polymer A having the structural unit represented by formula (1), contained in the surface layer of the electrophotographic photoreceptor of this disclosure, is preferably 16,000 to 100,000, from the viewpoint of improving the dispersibility of fluorine atom-containing resin particles and suppressing potential fluctuations. Furthermore, the weight-average molecular weight of polymer A having the structural unit represented by formula (1) is more preferably 18,000 to 80,000.

[0048] The weight-average molecular weight of polymer A having the structural unit shown in formula (1) above can be measured and calculated by the following method. (Weight-average molecular weight measurement by GPC) The weight-average molecular weight relating to this disclosure is measured by gel permeation chromatography (GPC) as follows. First, the sample is dissolved in tetrahydrofuran (THF) at room temperature for 24 hours. Then, the resulting solution is filtered through a solvent-resistant membrane filter, "Maeshori Disc" (manufactured by Tosoh Corporation), with a pore diameter of 0.2 μm, to obtain the sample solution. The sample solution is adjusted so that the concentration of components soluble in THF is approximately 0.8% by mass. This sample solution is then used for measurement under the following conditions. • Equipment: HLC8120 GPC (Detector: RI) (Manufactured by Tosoh Corporation) • Columns: Shodex KF-801, 802, 803, 804, 805, 806, 807 (7 columns, manufactured by Showa Denko) • Eluent: Tetrahydrofuran (THF) ·Flow rate: 1.0ml / min Oven temperature: 40.0℃ • Sample injection volume: 0.10 ml For calculating the molecular weight of the sample, a molecular weight calibration curve prepared using standard polystyrene resin (for example, "TSK Standard Polystyrene F-850, F-450, F-288, F-128, F-80, F-40, F-20, F-10, F-4, F-2, F-1, A-5000, A-2500, A-1000, A-500", manufactured by Tosoh Corporation) is used.

[0049] The content of polymer A having the structural unit shown in formula (1) in the surface layer relative to the fluorine atom-containing resin particles is preferably 2% by mass or more and 10% by mass or less, from the viewpoint of improving the dispersibility of the fluorine atom-containing resin particles and suppressing potential fluctuations. Furthermore, the content of polymer A having the structural unit shown in formula (1) in the surface layer relative to the fluorine atom-containing resin particles is more preferably 4% by mass or more and 8% by mass or less, from the viewpoint of improving dispersibility and suppressing potential fluctuations.

[0050] <Electrophotographic photoconductor> Figure 1 shows an example of the layer structure of the electrophotographic photoreceptor of this disclosure. In Figure 1, a base layer 102, a charge generation layer 103, a charge transport layer 104, and a surface layer 105 are laminated on a support 101. The photosensitive layer may be composed of a laminated photosensitive layer having a charge generation layer and a charge transport layer, or it may be composed of a single-layer photosensitive layer containing a charge generation material and a charge transport material.

[0051] The surface layer of the electrophotographic photoreceptor of this disclosure contains fluorine atom-containing resin particles, a binder material, and a polymer A having a structural unit represented by formula (1).

[0052] A method for manufacturing the electrophotographic photoreceptor according to this disclosure includes preparing coating solutions for each layer, applying the desired layers in order, and drying them. Examples of coating methods include immersion coating, spray coating, inkjet coating, roll coating, die coating, blade coating, curtain coating, wire bar coating, and ring coating. Among these, immersion coating is preferred from the viewpoint of efficiency and productivity.

[0053] The configuration of the electrophotographic photoreceptor described herein will be explained below. <Support> The support for the electrophotographic photoreceptor is preferably conductive (a conductive support). The support can take various shapes, such as cylindrical, belt-shaped, or sheet-shaped. A cylindrical support is preferred. The surface of the support may also be subjected to electrochemical treatments such as anodizing, blasting, or cutting. Suitable materials for the support include metal, resin, and glass. Examples of metals include aluminum, iron, nickel, copper, gold, stainless steel, and alloys thereof. Among these, an aluminum support made of aluminum is preferred. Furthermore, it is preferable to impart conductivity to resins and glass by processing them, such as by mixing or coating them with conductive materials.

[0054] <Conductive layer> A conductive layer may be provided on the support. By providing a conductive layer, scratches and irregularities on the surface of the support can be concealed, and light reflection on the surface of the support can be controlled. The conductive layer preferably contains conductive particles and a resin.

[0055] Examples of materials for conductive particles include metal oxides, metals, and carbon black. Examples of metal oxides include zinc oxide, aluminum oxide, indium oxide, silicon oxide, zirconium oxide, tin oxide, titanium oxide, strontium titanate, magnesium oxide, antimony oxide, and bismuth oxide. Examples of metals include aluminum, nickel, iron, nichrome, copper, zinc, and silver. Among these, it is preferable to use metal oxide particles as conductive particles, and it is more preferable to use titanium oxide particles, tin oxide particles, or zinc oxide particles. When using metal oxide particles as conductive particles, the surface of the metal oxide particles may be treated with a silane coupling agent or the like, or the metal oxide particles may be doped with elements such as phosphorus or aluminum, or their oxides. Furthermore, the conductive particles may have a laminated structure comprising core material particles and a coating layer covering those particles. Examples of core material particles include titanium oxide particles, barium sulfate particles, and zinc oxide particles. Examples of coating layer particles include metal oxide particles such as tin oxide. Furthermore, when metal oxide particles are used as conductive particles, their volume-average particle size is preferably 1 nm or more and 500 nm or less, and more preferably 3 nm or more and 400 nm or less.

[0056] Examples of resins include polyester resin, polycarbonate resin, polyvinyl acetal resin, acrylic resin, silicone resin, epoxy resin, melamine resin, polyurethane resin, phenolic resin, and alkyd resin. Furthermore, the conductive layer may further contain silicone oil, resin particles, a concealing agent such as titanium dioxide, etc.

[0057] A conductive layer can be formed by preparing a coating solution for a conductive layer containing the above-mentioned materials and solvents, forming this coating film on a support, and drying it. Examples of solvents used in the coating solution for a conductive layer include alcohol-based solvents, sulfoxide-based solvents, ketone-based solvents, ether-based solvents, ester-based solvents, and aromatic hydrocarbon-based solvents. Methods for dispersing conductive particles in the coating solution for a conductive layer include using a paint shaker, sand mill, ball mill, or liquid impaction type high-speed disperser.

[0058] The average thickness of the conductive layer is preferably 1 μm or more and 50 μm or less, and particularly preferably 3 μm or more and 40 μm or less.

[0059] <Underlayer> In this disclosure, an undercoat layer may be provided on the support or conductive layer. Providing an undercoat layer enhances the interlayer adhesion function and imparts a charge injection blocking function.

[0060] The undercoat layer preferably contains a resin. Alternatively, the undercoat layer may be formed as a cured film by polymerizing a composition containing a monomer having polymerizable functional groups. Examples of resins include polyester resin, polycarbonate resin, polyvinyl acetal resin, acrylic resin, epoxy resin, melamine resin, polyurethane resin, phenolic resin, polyvinylphenol resin, alkyd resin, polyvinyl alcohol resin, polyethylene oxide resin, polypropylene oxide resin, polyamide resin, polyamic acid resin, polyimide resin, polyamide-imide resin, and cellulose resin. Polymerizable functional groups found in monomers possessing polymerizable functional groups include isocyanate groups, blocked isocyanate groups, methylol groups, alkylated methylol groups, epoxy groups, metal alkoxide groups, hydroxyl groups, amino groups, carboxyl groups, thiol groups, carboxylic acid anhydride groups, and carbon-carbon double bond groups.

[0061] Furthermore, the undercoat layer may further contain electron transport materials, metal oxide particles, metal particles, conductive polymers, etc., for the purpose of improving electrical properties. Among these, electron transport materials and metal oxide particles are preferred. Examples of electron transport materials include quinone compounds, imide compounds, benzimidazole compounds, cyclopentadienylidene compounds, fluorenone compounds, xanthone compounds, benzophenone compounds, cyanovinyl compounds, aryl halides, silole compounds, and boron-containing compounds. An electron transport material having polymerizable functional groups may be used as the electron transport material, and a base layer may be formed as a cured film by copolymerizing it with the above-mentioned monomers having polymerizable functional groups. Examples of metal oxide particles include indium tin oxide, tin oxide, indium oxide, titanium oxide, strontium titanate, zinc oxide, and aluminum oxide. Silicon dioxide particles can also be used. Examples of metal particles include gold, silver, and aluminum. The metal oxide particles contained in the undercoat may be surface-treated using a surface treatment agent such as a silane coupling agent before use.

[0062] Common methods are used for surface treatment of metal oxide particles. Examples include dry and wet methods. The dry method involves adding an aqueous alcohol solution, an organic solvent solution, or an aqueous solution containing a surface treatment agent to metal oxide particles while stirring them in a high-speed mixer such as a Henschel mixer, then uniformly dispersing them and drying them. In the wet method, metal oxide particles and a surface treatment agent are stirred in a solvent or dispersed using a sand mill with glass beads or the like. After dispersion, the solvent is removed by filtration or vacuum distillation. After solvent removal, it is preferable to further bake the mixture at 100°C or higher.

[0063] The undercoat layer may further contain additives, such as known materials including metal particles like aluminum particles, conductive material particles like carbon black, charge transport materials, metal chelate compounds, and organometallic compounds.

[0064] The undercoat layer can be formed by preparing an undercoat coating solution containing the above-mentioned materials and solvents, forming this coating film on a support or conductive layer, and then drying and / or curing it.

[0065] Examples of solvents used in the coating liquid for the undercoat include organic solvents such as alcohols, sulfoxides, ketones, ethers, esters, aliphatic halogenated hydrocarbons, and aromatic compounds. In this disclosure, it is preferable to use alcohol-based or ketone-based solvents.

[0066] Dispersion methods for preparing coating liquids for the undercoat include methods using homogenizers, ultrasonic dispersers, ball mills, sand mills, roll mills, vibratory mills, attritors, and liquid impact type high-speed dispersers.

[0067] The average thickness of the undercoat layer is preferably 0.1 μm or more and 50 μm or less, more preferably 0.2 μm or more and 40 μm or less, and particularly preferably 0.3 μm or more and 30 μm or less.

[0068] <Photosensitive layer> The photosensitive layers of electrophotographic photoreceptors are mainly classified into (1) multilayer photosensitive layers and (2) single-layer photosensitive layers. (1) A multilayer photosensitive layer is a photosensitive layer having a charge generating layer containing a charge generating material and a charge transport layer containing a charge transport material. (2) A single-layer photosensitive layer is a photosensitive layer containing both a charge generating material and a charge transport material.

[0069] (1) Stacked photosensitive layer The stacked photosensitive layer comprises a charge generation layer and a charge transport layer.

[0070] (1-1) Charge generation layer The charge generation layer preferably contains a charge generation material and a resin.

[0071] Examples of charge-generating materials include azo pigments, perylene pigments, polycyclic quinone pigments, indigo pigments, and phthalocyanine pigments. Among these, azo pigments and phthalocyanine pigments are preferred. Among phthalocyanine pigments, oxytitanium phthalocyanine pigments, chlorogallium phthalocyanine pigments, and hydroxygallium phthalocyanine pigments are preferred. The content of the charge generating material in the charge generating layer is preferably 40% to 85% by mass, and more preferably 60% to 80% by mass, relative to the total mass of the charge generating layer.

[0072] Examples of resins include polyester resin, polycarbonate resin, polyvinyl acetal resin, polyvinyl butyral resin, acrylic resin, silicone resin, epoxy resin, melamine resin, polyurethane resin, phenolic resin, polyvinyl alcohol resin, cellulose resin, polystyrene resin, polyvinyl acetate resin, and polyvinyl chloride resin. Among these, polyvinyl butyral resin is more preferred.

[0073] Furthermore, the charge generation layer may contain additives such as antioxidants and ultraviolet absorbers. Specifically, these include hindered phenol compounds, hindered amine compounds, sulfur compounds, phosphorus compounds, and benzophenone compounds.

[0074] The charge generation layer can be formed by preparing a coating solution for the charge generation layer containing the above-mentioned materials and solvents, forming this coating film on the undercoat layer, and drying it. Examples of solvents used in the coating solution include alcohol-based solvents, sulfoxide-based solvents, ketone-based solvents, ether-based solvents, ester-based solvents, and aromatic hydrocarbon-based solvents.

[0075] The average thickness of the charge generation layer is preferably 0.1 μm or more and 1 μm or less, and more preferably 0.15 μm or more and 0.4 μm or less.

[0076] (1-2) Charge transport layer The charge transport layer preferably contains a charge transport material and one binder material.

[0077] Examples of charge transport materials include polycyclic aromatic compounds, heterocyclic compounds, hydrazone compounds, styryl compounds, enamine compounds, triarylamine compounds, and resins having groups derived from these substances. Among these, triarylamine compounds are preferred. The content of the charge transport material in the charge transport layer is preferably 25% by mass or more and 70% by mass or less, and more preferably 30% by mass or more and 55% by mass or less, based on the total mass of the charge transport layer.

[0078] A thermoplastic resin (hereinafter also referred to as "resin") is used as the binding material. Examples of thermoplastic resins include polyester resin, polycarbonate resin, acrylic resin, and polystyrene resin. Among these, polycarbonate resin and polyester resin are preferred. Polyarylate resin is particularly preferred among polyester resins. The content ratio (mass ratio) of the charge transport material to the resin is preferably 4:10 to 20:10, and more preferably 5:10 to 12:10.

[0079] When the protective layer described later is not provided, the charge transport layer becomes the surface layer. In this case, the charge transport layer contains fluorine atom-containing resin particles, a binder material, and a polymer A having a structural unit represented by the above formula (1). Further, the content ratio of the fluorine atom-containing resin particles in the charge transport layer is preferably 5% by mass or more and 40% by mass or less with respect to the total mass of the charge transport layer. Further, the content ratio of the fluorine atom-containing resin particles in the charge transport layer is more preferably 5% by mass or more and 15% by mass or less from the viewpoints of improving the uniformity of dispersion of the fluorine atom-containing resin particles and improving the abrasion resistance, and still more preferably 7% by mass or more and 10% by mass or less.

[0080] In the present disclosure, the surface layer preferably contains a thermoplastic resin as a binder material and a charge transport substance, and the thermoplastic resin is a polycarbonate resin or a polyarylate resin. Furthermore, in the present disclosure, it is preferable that the charge transport substance is any one or both of the compounds represented by the following formula (3) and the following formula (4).

Chemical formula

Chemical formula

[0081] Furthermore, the charge transport layer may contain additives such as antioxidants, ultraviolet absorbers, plasticizers, and leveling agents. Specifically, examples include hindered phenol compounds, hindered amine compounds, sulfur compounds, phosphorus compounds, benzophenone compounds, siloxane-modified resins, silicone oils, polystyrene resin particles, polyethylene resin particles, and boron nitride particles.

[0082] The charge transport layer can be formed by preparing a coating solution for the charge transport layer containing the above-mentioned materials and solvents, forming this coating film on the charge generating layer, and drying it. Examples of solvents used in the coating solution include alcohol-based solvents, ketone-based solvents, ether-based solvents, ester-based solvents, and aromatic hydrocarbon-based solvents. Among these solvents, ether-based solvents or aromatic hydrocarbon-based solvents are preferred.

[0083] The average thickness of the charge transport layer is preferably 5 μm to 50 μm, more preferably 8 μm to 40 μm, and particularly preferably 10 μm to 30 μm.

[0084] (2) Single-layer photosensitive layer A single-layer photosensitive layer can be formed by preparing a coating solution for a photosensitive layer containing a charge generating substance, a charge transporting substance, a resin, and a solvent, forming this coating film on an undercoat layer, and drying it. The charge generating substance, charge transporting substance, and resin are the same as the examples of materials in "(1) Multilayer Photosensitive Layer" above.

[0085] <Protective layer> In this invention, a protective layer may be provided on the photosensitive layer. Providing a protective layer can improve durability.

[0086] The protective layer may be formed as a cured film by polymerizing a composition containing a monomer having a polymerizable functional group, which serves as a raw material for the binder. Examples of reactions include thermal polymerization, photopolymerization, and radiation polymerization. Examples of polymerizable functional groups in monomers having polymerizable functional groups include isocyanate groups, blocked isocyanate groups, methylol groups, alkylmethylol groups, epoxy groups, metal alkoxyl groups, hydroxyl groups, amino groups, carboxyl groups, thiol groups, carboxylic acid anhydride groups, and groups containing carbon-carbon double bonds. Examples of groups containing carbon-carbon double bonds include acryloyl groups and methacryloyl groups. Monomers having charge transport ability may be used as monomers having polymerizable functional groups.

[0087] When a protective layer is provided, the protective layer becomes the surface layer of the electrophotographic photoreceptor. In this case, the protective layer contains fluorine atom-containing resin particles, a binder material, and polymer A having the structural unit shown in formula (1). When no protective layer is provided, in the case of an electrophotographic photoreceptor having a multilayer photosensitive layer, the charge transport layer is the surface layer, and in the case of an electrophotographic photoreceptor having a single-layer photosensitive layer, the photosensitive layer is the surface layer.

[0088] The protective layer may contain additives such as antioxidants, UV absorbers, plasticizers, and leveling agents. Specifically, these include hindered phenol compounds, hindered amine compounds, sulfur compounds, phosphorus compounds, benzophenone compounds, siloxane-modified resins, and silicone oils.

[0089] The protective layer can be formed by preparing a protective coating solution containing the above-mentioned materials and solvents, forming this coating film on the photosensitive layer, and drying and / or curing it. Examples of solvents used in the coating solution include alcohol-based solvents, ketone-based solvents, ether-based solvents, sulfoxide-based solvents, ester-based solvents, and aromatic hydrocarbon-based solvents.

[0090] The average thickness of the protective layer is preferably 0.5 μm to 10 μm, and more preferably 1 μm to 7 μm.

[0091] One preferred form of the protective layer is one that includes a cured product of a composition containing a hole-transporting compound having polymerizable functional groups. The hole-transporting compound having a polymerizable functional group is preferably a compound represented by the following formula (CT-1) or (CT-2). [ka] In the above formula (CT-1), Ar 11 ~Ar 13 Each of these is independently a substituted aryl group or an unsubstituted aryl group. The substituents that the substituted aryl group may have are alkyl groups having 1 to 6 carbon atoms, or monovalent functional groups represented by any of the following formulas (P-1) to (P-3). However, the compound represented by formula (CT-1) has at least one monovalent functional group represented by any of the following formulas (P-1) to (P-3). [ka] In the above formula (CT-2), Ar 21 ~Ar 24 These are, independently, a substituted aryl group or an unsubstituted aryl group, Ar 25 This is a substituted aryl group or an unsubstituted aryl group. The substituents that the substituted aryl group may have are alkyl groups having 1 to 6 carbon atoms, or monovalent functional groups represented by the following formulas (P-1) to (P-3). The substituents that the substituted aryl group may have are alkyl groups having 1 to 6 carbon atoms, or monovalent functional groups represented by the following formulas (P-1) to (P-3). However, the compound represented by formula (CT-2) has at least one monovalent functional group represented by any of the following formulas (P-1) to (P-3). [ka] In the above equation (P-1), Z 11 X is a single bond or an alkylene group having 1 to 6 carbon atoms. 11 This is either a hydrogen atom or a methyl group. [ka] In the above equation (P-2), Z 21 This is a single bond or an alkylene group having 1 to 6 carbon atoms. [ka] In the above equation (P-3), Z 31 This is a single bond or an alkylene group having 1 to 6 carbon atoms.

[0092] In this case, the protective layer contains fluorine atom-containing resin particles, a binder, and polymer A having the structural unit represented by formula (1) above. Furthermore, the content of fluorine atom-containing resin particles in the protective layer is preferably 5% by mass or more and 40% by mass or less based on the total mass of the protective layer. Moreover, the content of fluorine atom-containing resin particles in the protective layer is more preferably 20% by mass or more and 40% by mass or less, from the viewpoint of improving the uniformity of the dispersion of fluorine atom-containing resin particles and improving wear resistance, and even more preferably 25% by mass or more and 35% by mass or less.

[0093] The protective layer of the electrophotographic photoreceptor of this disclosure may contain a cured product of a charge transporting compound as described later as a binder material, at least one triazine compound selected from the group consisting of guanamine compounds and melamine compounds, fluorine atom-containing resin particles, and polymer A having a structural unit represented by formula (1).

[0094] The protective layer of the present invention may further be a mixture of phenolic resin, melamine resin, urea resin, alkyd resin, etc. In addition, to improve strength, compounds with more functional groups in a single molecule, such as spiroacetal-based guanamine resin (e.g., "CTU-guanamine" (Ajinomoto Fine Techno Co., Ltd.)), may be used.

[0095] <Charge transport compound> In this disclosure, a charge-transporting compound is a compound having an organic group derived from a compound having charge-transporting ability, and at least one polymerizable substituent (hereinafter also referred to as a "functional group").

[0096] Examples of functional groups found in charge-transporting compounds include hydroxyl groups (-OH), methylol groups (-CH2OH), methoxy groups (-OCH3), amino groups (-NH2), thiol groups (-SH), and carboxyl groups (-COOH). Of these, it is preferable that at least one functional group is selected from methylol groups and methoxy groups.

[0097] Among the organic groups derived from compounds with charge transport ability, arylamine derivatives are preferred as compounds with charge transport ability. Examples of arylamine derivatives include triphenylamine derivatives and tetraphenylbenzidine derivatives.

[0098] Specific examples of charge-transporting compounds include the following: [ka] [ka]

[0099] In particular, the protective layer preferably contains a guanamine compound represented by formula (A) below, a melamine compound represented by formula (B) below, and at least one triazine compound selected from these. [ka] In formula (A), R 101 ~R 104 Each of these independently represents a hydrogen atom, a hydroxymethyl group, or an alkoxymethyl group, and R 101 ~R 104 At least one of them is a hydroxymethyl group or an alkoxymethyl group, R105 This represents an alkyl group which may have substituents, a phenyl group which may have substituents, or a cycloalkyl group which may have substituents. R 105 The substituents that the alkyl group, phenyl group, and cycloalkyl group shown may each have are alkyl groups and alkoxy groups. [ka] In formula (B), R 201 ~R 206 Each of these independently represents a hydrogen atom, a hydroxymethyl group, an alkoxymethyl group, or an alkoxy group, and R 201 ~R 206 At least one of them is a hydroxymethyl group, an alkoxymethyl group, or an alkoxy group.

[0100] The protective layer contains at least one triazine compound selected from the guanamine compound represented by formula (A) and the melamine compound represented by formula (B), thereby improving the film strength. Furthermore, since these compounds have nitrogen atoms that contribute to electron transport, the electron transport performance in the protective layer is improved. A triazine compound refers to a compound containing a triazine ring, and in the present invention, it is a guanamine compound or a melamine compound.

[0101] The cured product of the charge-transporting compound (a) and triazine compound (b) contained in the surface layer of the electrophotographic photoreceptor of the present invention is preferably a cured product obtained by reacting b:a = 1:3 to 1:300 (molar ratio). From the viewpoint of surface layer wear resistance, it is more preferable that b:a = 1:100 or less, and from the viewpoint of suppressing potential fluctuations due to repeated use, it is more preferable that b:a = 1:5 or more.

[0102] In this case, the protective layer contains fluorine atom-containing resin particles and polymer A having the structural unit represented by formula (1) above. Furthermore, the content of fluorine atom-containing resin particles in the protective layer is preferably 5% by mass or more and 40% by mass or less based on the total mass of the protective layer. Moreover, the content of fluorine atom-containing resin particles in the protective layer is more preferably 5% by mass or more and 15% by mass or less, from the viewpoint of improving the uniformity of the dispersion of fluorine atom-containing resin particles and improving wear resistance, and even more preferably 7% by mass or more and 12% by mass or less.

[0103] Commercially available guanamine compounds include Super Beccamine L-148-55, Super Beccamine 13-535, Super Beccamine L-145-60, Super Beccamine TD-126 (all manufactured by DIC Corporation), and Nikalac BL-60 and Nikalac BX-4000 (both manufactured by Sanwa Chemical Co., Ltd.).

[0104] Commercially available melamine compounds include Super Melami No. 90 (manufactured by NOF Corporation), Super Beccamine TD-139-60 (manufactured by DIC Corporation), Yuban 2020 (manufactured by Mitsui Chemicals), Sumitex Resin M-3 (manufactured by Sumitomo Chemical Co., Ltd.), and Nikalac MW-30 (manufactured by Sanwa Chemical Co., Ltd.).

[0105] <Surface treatment of electrophotographic photoreceptors> In this disclosure, the surface of the electrophotographic photoreceptor may be processed. By processing the surface, the behavior of the cleaning means (cleaning blade) that comes into contact with the electrophotographic photoreceptor can be made more stable. Methods of surface processing include pressing a mold having protrusions onto the surface of the electrophotographic photoreceptor to transfer the shape, creating an uneven shape by mechanical polishing, or roughening the surface of the electrophotographic photoreceptor by impacting it with powder. By providing recesses or protrusions on the surface layer of the electrophotographic photoreceptor in this way, the behavior of the cleaning means that comes into contact with the electrophotographic photoreceptor can be made more stable.

[0106] The recesses or protrusions may be formed over the entire surface of the electrophotographic photoreceptor, or on a portion of the surface of the electrophotographic photoreceptor. If the recesses or protrusions are formed on a portion of the surface of the electrophotographic photoreceptor, it is preferable that the recesses or protrusions are formed over at least the entire contact area with the cleaning means (cleaning blade).

[0107] When forming a recess, a mold having a convex portion corresponding to the recess is pressed against the surface of the electrophotographic photoreceptor, and the shape is transferred, thereby forming a recess on the surface of the electrophotographic photoreceptor.

[0108] <Abrasive tools used for mechanical polishing> Mechanical polishing can be performed using known methods. Generally, a polishing tool is brought into contact with an electrophotographic photoreceptor, and either one or both of the tools are moved relative to each other to polish the surface of the electrophotographic photoreceptor. The polishing tool is a polishing member having a layer on a base material in which abrasive particles are dispersed in a binder resin.

[0109] Examples of abrasive particles include aluminum oxide, chromium oxide, diamond, iron oxide, cerium oxide, corundum, silica, silicon nitride, boron nitride, molybdenum carbide, silicon carbide, tungsten carbide, titanium carbide, and silicon oxide. The particle size of the abrasive particles is preferably 0.01 μm to 50 μm, and more preferably 1 μm to 15 μm. If the particle size of the abrasive particles is too small, the polishing power will be weak, and it will be difficult to increase the F / C ratio, which is the mole fraction ratio of fluorine atoms (F) to carbon atoms (C) of the surface layer at the outermost surface of the electrophotographic photoreceptor, as measured by X-ray photoelectron spectroscopy. These abrasive particles can be used individually or in mixtures of two or more types. When mixing two or more types, the materials and particle sizes may be different or the same.

[0110] As the binder resin for dispersing abrasive particles used in polishing tools, known thermoplastic resins, thermosetting resins, reactive resins, electron beam curing resins, ultraviolet curing resins, visible light curing resins, and antifungal resins can be used. Examples of thermoplastic resins include vinyl chloride resin, polyamide resin, polyester resin, polycarbonate resin, amino resin, styrene-butadiene copolymer, urethane elastomer, and polyamide-silicone resin. Examples of thermosetting resins include phenolic resin, phenoxy resin, epoxy resin, polyurethane resin, polyester resin, silicone resin, melamine resin, and alkyd resin. An isocyanate-based curing agent may also be added to the thermoplastic resin.

[0111] The thickness of the layer formed by dispersing abrasive grains in the binder resin of the polishing tool is preferably between 1 μm and 100 μm. If the thickness is too thick, unevenness in the thickness is likely to occur, resulting in uneven surface roughness of the electrophotographic photoreceptor being polished. On the other hand, if the thickness is too thin, the abrasive grains are more likely to fall off.

[0112] The shape of the base material of the polishing tool is not particularly limited. In the embodiments of this disclosure, a sheet-like base material was used to efficiently polish a cylindrical electrophotographic photoreceptor, but other shapes may also be used. (Hereinafter, the polishing tool of this disclosure will also be referred to as the "polishing sheet.") The material of the base material of the polishing tool is also not particularly limited. For example, the material of the sheet-like base material may be paper, woven fabric, nonwoven fabric, or plastic film.

[0113] The polishing tool can be obtained by coating a substrate with a paint mixture in which the above-mentioned abrasive grains, binder resin, and solvent capable of dissolving the binder resin are mixed and dispersed, and then drying the mixture.

[0114] <Polishing equipment> An example of the polishing apparatus for electrophotographic photoreceptors described herein is shown in Figure 2. Figure 2 shows an apparatus for polishing a cylindrical electrophotographic photoreceptor using a polishing sheet. In Figure 2, the polishing sheet 2-1 is wound around a hollow shaft 2-6, and a motor (not shown) is positioned so that tension is applied to the polishing sheet 2-1 in the opposite direction to the direction in which the polishing sheet 2-1 is fed to the shaft 2-6. The polishing sheet 2-1 is fed in the direction of the arrow, passes through guide rollers 2-2a and 2-2b to a backup roller 2-3, and after polishing, the polishing sheet 2-1 is wound onto a winding means 2-5 by a motor (not shown) via guide rollers 2-2c and 2-2d. Polishing is performed by constantly pressing the polishing sheet 2-1 against the workpiece (electrophotographic photoreceptor before polishing) 2-4. Since the polishing sheet 2-1 is often insulating, it is preferable to use a material that is grounded or conductive at the contact points of the polishing sheet 2-1.

[0115] The feed speed of the abrasive sheet 2-1 is preferably in the range of 10 to 1000 mm / min. If the feed rate is too low, the binder resin may adhere to the surface of the abrasive sheet 2-1, which may result in deep scratches on the surface of the workpiece 2-4.

[0116] The workpiece 2-4 is placed facing the backup roller 2-3 via the abrasive sheet 2-1. The backup roller 2-3 is preferably elastic in order to improve the uniformity of the surface roughness of the workpiece 2-4. In this process, the workpiece 2-4 and the backup roller 2-3 are pressed together for a predetermined time at a desired setting value via the abrasive sheet 2-1, and the surface of the workpiece 2-4 is polished. The rotation direction of the workpiece 2-4 may be the same as the direction in which the abrasive sheet 2-1 is fed, or it may be opposite. Furthermore, the rotation direction may be changed during polishing.

[0117] The pressure applied by the backup rollers 2-3 against the workpiece 2-4 depends on the hardness of the backup rollers 2-3 and the polishing time, but is approximately 0.005 to 15 N / m 2 It is preferable.

[0118] The surface roughness of the electrophotographic photoreceptor can be adjusted by appropriately selecting the feed speed of the polishing sheet 2-1, the pressing pressure of the backup roller 2-3, the abrasive grain type of the polishing sheet, the film thickness of the binder resin of the polishing sheet, the thickness of the base material, etc.

[0119] <Measurement of the maximum height Rmax in JIS B0601 1982> The surface roughness of the electrophotographic photoreceptor can be measured by known means. For example, the following can be mentioned. Surface roughness meters such as the Surfcoader SE3500 type surface roughness measuring instrument manufactured by Kosaka Laboratory Ltd. A non-contact three-dimensional surface measuring machine, Micromap 557N, manufactured by Hishikawa System Co., Ltd. Microscopes capable of acquiring three-dimensional shapes, such as the ultra-depth shape measuring microscopes VK-8550 and VK-9000 manufactured by Keyence Corporation.

[0120] In the present disclosure, among the indexes of surface roughness, the maximum height Rmax in JIS B0601 1982 defined by the Japanese Industrial Standard JIS is used as the polishing depth L (μm). Also, in the present disclosure, for the range of the 5 mm square section of the electrophotographic photoreceptor cut out as a specimen for the X-ray photoelectron spectroscopy described later, Rmax is measured in advance. The measurement is performed arbitrarily at three locations within the range of the 5 mm square of the cut-out electrophotographic photoreceptor, and the average value is adopted as the polishing depth L (μm).

[0121] <Process cartridge, electrophotographic apparatus> The electrophotographic photoreceptor of the present disclosure may be one of the components of a process cartridge or an electrophotographic apparatus. The process cartridge integrally supports the electrophotographic photoreceptor described so far and at least one means selected from the group consisting of charging means, developing means, transfer means, and cleaning means, and is detachable from the electrophotographic apparatus main body. Further, the electrophotographic apparatus is characterized by having the electrophotographic photoreceptor, charging means, exposure means, developing means, and transfer means described so far.

[0122] Figure 3 shows a process cartridge configuration equipped with the electrophotographic photoreceptor of this disclosure, and Figure 4 shows an example of a schematic configuration of an electrophotographic apparatus having the process cartridge of Figure 3.

[0123] In Figure 3, the cylindrical electrophotographic photoreceptor 1 is driven to rotate at a predetermined peripheral speed in the direction of the arrow. The peripheral surface of the rotating electrophotographic photoreceptor 1 is uniformly charged to a predetermined positive or negative potential by the charging means 2. Next, the charged peripheral surface of the electrophotographic photoreceptor 1 receives exposure light (image exposure light) 3 output from an exposure means (not shown), such as slit exposure or laser beam scanning exposure. In this way, an electrostatic latent image corresponding to the desired image is sequentially formed on the peripheral surface of the electrophotographic photoreceptor 1. The voltage applied to the charging means (charging roller, etc.) 2 may be either a voltage with an AC component superimposed on a DC component, or a voltage with only a DC component.

[0124] The electrostatic latent image formed on the circumferential surface of the electrophotographic photoreceptor 1 is developed by the toner contained in the developer of the developing means 4 to form a toner image. Next, the toner image formed and supported on the circumferential surface of the electrophotographic photoreceptor 1 is sequentially transferred to the transfer material (paper, intermediate transfer material, etc.) 6 by the transfer bias from the transfer means (transfer roller, etc.) 5. The transfer material 6 is fed in synchronization with the rotation of the electrophotographic photoreceptor 1.

[0125] After toner image transfer, the surface of the electrophotographic photoreceptor 1 is treated to remove static electricity by pre-exposure light 7 from a pre-exposure means (not shown), and then cleaned by a cleaning means 8 to remove any remaining toner. The electrophotographic photoreceptor 1 is then repeatedly used for image formation. The pre-exposure means may be performed before or after the cleaning process, and is not necessarily required.

[0126] The electrophotographic photoreceptor 1 may be mounted in an electrophotographic device such as a copier or a laser beam printer. Alternatively, a process cartridge 9 may be constructed by housing and supporting multiple components, such as the electrophotographic photoreceptor 1, charging means 2, developing means 4, and cleaning means 8, in a container, and making it detachable from the electrophotographic device body. In Figure 3, the electrophotographic photoreceptor 1, charging means 2, developing means 4, and cleaning means 8 are supported as a single unit, forming a process cartridge 9 that is detachable from the electrophotographic device body.

[0127] Next, an electrophotographic apparatus equipped with the electrophotographic photoreceptor of this disclosure will be described. Figure 4 shows an example of the configuration of the electrophotographic apparatus of this disclosure. Process cartridges 17 for yellow, 18 for magenta, 19 for cyan, and 20 for black, corresponding to yellow, magenta, cyan, and black respectively, are arranged side by side along the intermediate transfer body 10. The diameter, constituent materials, developer, charging method, and other means of the electrophotographic photoreceptor do not necessarily have to be the same for each color.

[0128] When the image formation operation begins, toner images of each color are sequentially superimposed on the intermediate transfer body 10 according to the image formation process described above. In parallel, the transfer paper 11 is fed from the paper tray 13 by the paper feed path 12 and is fed to the secondary transfer means 14 in time with the rotation of the intermediate transfer body. The toner image on the intermediate transfer body 10 is transferred to the transfer paper 11 by the transfer bias from the secondary transfer means 14. The toner image transferred onto the transfer paper 11 is transported along the paper feed path 12, fixed onto the transfer paper by the fixing means 15, and then discharged from the paper discharge unit 16.

[0129] The electrophotographic photoreceptor of this disclosure can be used in laser beam printers, LED printers, copiers, facsimile machines, and multifunction devices thereof. [Examples]

[0130] The present disclosure will be described in further detail below using examples and comparative examples, but will not be limited thereto. In the following descriptions of examples, "parts" refers to mass unless otherwise specified.

[0131] <Synthesis of polymer A having the structural unit shown in formula (1)> The polymer A having the structural unit represented by formula (1) in this disclosure (hereinafter also referred to as "graft copolymer") was synthesized as follows. The acrylate compound and macromonomer compound used in the following synthesis example can be produced, for example, by referring to Japanese Patent Application Publication No. 2009-104145.

[0132] (Graft copolymer 1) 50 parts of 1H,1H-perfluoro(6-oxadecanoyl)acrylate (manufactured by Sigma-Aldrich), 75 parts of the macromonomer represented by the following formula (A-1) (number average molecular weight 6,000), 0.437 parts of 1,1'-azobis(1-acetoxy-1-phenylethane) (trade name: OTAZO-15, manufactured by Otsuka Chemical Co., Ltd.), and 338 parts of n-butyl acetate were mixed in a glass flask equipped with a stirrer, reflux condenser, nitrogen gas inlet tube, constant temperature bath, and thermometer at 20°C under a nitrogen atmosphere for 30 minutes. The reaction was then heated to 85-90°C and allowed to proceed for 5 hours. The reaction was stopped by cooling with ice, and a precipitate was obtained by adding 1500 parts by mass of 2-propanol. This precipitate was washed with a mixed solvent of n-butyl acetate and 2-propanol in a ratio of 1:5, and dried at a temperature of 80°C under reduced pressure of 1325 Pa or less for 3 hours to obtain graft copolymer 1. [ka]

[0133] (Graft copolymer 2) Graft copolymer 2 was obtained in the same manner as graft copolymer 1, except that 0.819 parts of 1,1'-azobis(1-acetoxy-1-phenylethane) were added.

[0134] (Graft copolymer 3) Graft copolymer 3 was obtained in the same manner as graft copolymer 1, except that 0.728 parts of 1,1'-azobis(1-acetoxy-1-phenylethane) were added.

[0135] (Graft copolymer 4) Graft copolymer 4 was obtained in the same manner as graft copolymer 1, except that 0.164 parts of 1,1'-azobis(1-acetoxy-1-phenylethane) were added.

[0136] (Graft copolymer 5) Graft copolymer 5 was obtained in the same manner as graft copolymer 1, except that 0.131 parts of 1,1'-azobis(1-acetoxy-1-phenylethane) were added.

[0137] (Graft copolymer 6) Graft copolymer 6 was obtained in the same manner as graft copolymer 1, except that 0.119 parts of 1,1'-azobis(1-acetoxy-1-phenylethane) were added.

[0138] (Graft copolymer 7) Graft copolymer 7 was obtained in the same manner as graft copolymer 1, except that 0.874 parts of 1,1'-azobis(1-acetoxy-1-phenylethane) were added.

[0139] (Graft copolymer 8) Graft copolymer 8 was obtained in the same manner as graft copolymer 1, except that 25 parts of 1H,1H-perfluoro(6-oxanonanyl)acrylate and 300 parts of macromonomer AA-6 were replaced.

[0140] (Graft copolymer 9) Graft copolymer 9 was obtained in the same manner as graft copolymer 1, except that 35 parts of 1H,1H-perfluoro(6-oxanonanyl)acrylate and 180 parts of macromonomer AA-6 were replaced.

[0141] (Graft copolymer 10) Graft copolymer 10 was obtained in the same manner as graft copolymer 1, except that 56.25 parts of 1H,1H-perfluoro(6-oxanonanyl)acrylate and 75 parts of macromonomer AA-6 were replaced.

[0142] (Graft copolymer 11) Graft copolymer 11 was obtained in the same manner as graft copolymer 1, except that 20 parts of 1H,1H-perfluoro(6-oxanonanyl)acrylate and 360 parts of macromonomer AA-6 were replaced.

[0143] (Graft copolymer 12) Graft copolymer 12 was obtained in the same manner as graft copolymer 1, except that 50 parts of 1H,1H-perfluoro(6-oxanonanyl)acrylate and 30 parts of macromonomer AA-6 were replaced.

[0144] (Graft copolymer 13) Graft copolymer 13 was obtained in the same manner as graft copolymer 1, except that 1H,1H-perfluoro(6-oxadecanoyl)acrylate was replaced with 40 parts of 1H,1H-perfluoro(3-dimethyl-4-oxaheptanoyl)acrylate and 30 parts of macromonomer AA-6.

[0145] (Graft copolymer 14) Graft copolymer 14 was obtained in the same manner as graft copolymer 1, except that 1H,1H-perfluoro(6-oxadecanoyl)acrylate was replaced with 55 parts of 1H,1H-perfluoro(6-oxaundecanoyl)acrylate and 30 parts of macromonomer AA-6.

[0146] (Graft copolymer 15) Graft copolymer 15 was obtained in the same manner as graft copolymer 1, except that 1H,1H-perfluoro(6-oxadecanoyl)acrylate was replaced with 60 parts of 1H,1H-perfluoro(7-oxadodecanoyl)acrylate and 30 parts of macromonomer AA-6.

[0147] (Graft copolymer 16) Graft copolymer 16 was obtained in the same manner as graft copolymer 1, except that 1H,1H-perfluoro(6-oxadecanoyl)acrylate was replaced with 60 parts of 1H,1H,2H,2H-perfluoro(8-oxatridecanoyl)acrylate and 75 parts of macromonomer AA-6.

[0148] (Graft copolymer 17) Graft copolymer 17 was obtained in the same manner as graft copolymer 1, except that 1H,1H-perfluoro(6-oxadecanoyl)acrylate was replaced with 45 parts of 1H,1H-perfluoro(3-dimethyl-4-oxaoctanoyl)acrylate and 75 parts of macromonomer AA-6.

[0149] (Graft copolymer 18) Graft copolymer 18 was obtained in the same manner as graft copolymer 1, except that 1H,1H-perfluoro(6-oxadecanoyl)acrylate was replaced with 45 parts of 1H,1H-perfluoro(2-dimethyl-3-oxaoctanoyl)acrylate and 75 parts of macromonomer AA-6.

[0150] (Graft copolymer 19) Graft copolymer 19 was obtained in the same manner as graft copolymer 1, except that 1H,1H-perfluoro(6-oxadecanoyl)acrylate was replaced with 45 parts of 1H,1H-perfluoro(8-oxanonanoyl)acrylate and 75 parts of macromonomer AA-6.

[0151] (Graft copolymer 20) Graft copolymer 20 was obtained in the same manner as graft copolymer 1, except that 1H,1H-perfluoro(6-oxadecanoyl)acrylate was replaced with 45 parts of 1H,1H-perfluoro(3-oxanonanoyl)acrylate and 75 parts of macromonomer AA-6.

[0152] (Graft copolymer 21) Graft copolymer 21 was obtained in the same manner as graft copolymer 1, except that 1H,1H-perfluoro(6-oxadecanoyl)acrylate was changed to 35 parts of 1H,1H-perfluoro(2-dimethyl-3-oxahexanoyl)acrylate and 75 parts of macromonomer AA-6.

[0153] (Graft copolymer 22) Graft copolymer 22 was obtained in the same manner as graft copolymer 1, except that 1H,1H-perfluoro(6-oxadecanoyl)acrylate was changed to 35 parts of 1H,1H-perfluoro(2-oxaheptanoyl)acrylate and 75 parts of macromonomer AA-6.

[0154] (Graft copolymer 23) Graft copolymer 23 was obtained in the same manner as graft copolymer 1, except that 1H,1H-perfluoro(6-oxadecanoyl)acrylate was changed to 50 parts of 1H,1H,2H,2H,3H,3H-perfluoro(5-dimethyl-6-oxadecanoyl)acrylate and 75 parts of macromonomer AA-6.

[0155] The obtained graft copolymers 1 to 23 were measured by GPC in the above-described method, and the weight average molecular weight was calculated. The results are shown in Table 3.

[0156]

Table 3

[0157] <Fabrication of electrophotographic photoreceptor> [Example 1-1] (Support 1) As the support (conductive support), a cylindrical aluminum cylinder (JIS-A3003, aluminum alloy, outer diameter 30.6 mm, length 370 mm, wall thickness 1 mm) obtained by cutting was used. Ultrasonic cleaning was performed in a cleaning solution containing a detergent (trade name: Chemicol CT, manufactured by Tokiwa Chemical Co., Ltd.) in pure water, and then the cleaning solution was rinsed off. Subsequently, ultrasonic cleaning was performed in pure water for degreasing treatment, and this was designated as Support 1.

[0158] (Bottom layer 1) Zinc oxide particles (specific surface area: 19 m²) 2 / g, powder resistance: 4.7×10 6 100 parts of (Ω·cm) were mixed with 500 parts of toluene and stirred. 0.8 parts of a silane coupling agent (compound name: N-2-(aminoethyl)-3-aminopropylmethyldimethoxysilane, trade name: KBM602, manufactured by Shin-Etsu Chemical Co., Ltd.) were added, and the mixture was stirred for 6 hours. Subsequently, the toluene was removed by distillation under reduced pressure, and the mixture was heated and dried at 130°C for 6 hours to obtain surface-treated zinc oxide particles A.

[0159] Next, 15 parts of butyral (trade name: BM-1, manufactured by Sekisui Chemical Co., Ltd.) and 15 parts of blocked isocyanate (trade name: Duranate TPA-B80E, non-volatile content 80% by mass, manufactured by Asahi Kasei Chemicals Corporation) were dissolved in a mixed solvent of 73.5 parts of methyl ethyl ketone and 73.5 parts of 1-butanol. To this solution, 80.8 parts of surface-treated zinc oxide particles A and 0.81 parts of 2,3,4-trihydroxybenzophenone (manufactured by Tokyo Chemical Industry Co., Ltd.) were added, and the mixture was dispersed for 3 hours at a 23±3°C atmosphere using a sand mill apparatus with glass beads with a diameter of 0.8 mm. After dispersion treatment, 0.01 parts of silicone oil (product name: SH28PA, manufactured by Toray Dow Corning Co., Ltd. (formerly Toray Dow Corning Silicone Co., Ltd.)) and 5.6 parts of cross-linked polymethyl methacrylate (PMMA) particles (product name: Techpolymer SSX-103, manufactured by Sekisui Chemical Co., Ltd., average primary particle size: 3 μm) were added and stirred to prepare a coating solution for the undercoat layer. The obtained undercoating solution for the undercoat layer was applied to the support 1 by immersion to form a coating film, and the coating film was dried at 160°C for 30 minutes to form an undercoat layer 1 with a thickness of 18 μm.

[0160] (Charge generation layer 1) Four parts of hydroxygallium phthalocyanine crystals (charge-generating material) in a crystalline form having strong peaks at 7.4° and 28.1° of the Bragg angle 2θ±0.2° in CuKα characteristic X-ray diffraction, and 0.04 parts of the compound represented by the following formula (E) were added to a solution prepared by dissolving 2 parts of polyvinyl butyral (trade name: S-Rec BX-1, manufactured by Sekisui Chemical Co., Ltd.) in 100 parts of cyclohexanone. Subsequently, the mixture was dispersed for 1 hour in a sand mill using 1 mm diameter glass beads under an atmosphere of 23±3°C. After dispersion, 100 parts of ethyl acetate were added to prepare a coating solution for the charge-generating layer. This charge generation layer coating solution was applied to the undercoat layer 1 by immersion, and the resulting coating film was dried at 90°C for 10 minutes to form a charge generation layer 1 with a thickness of 0.15 μm. [ka]

[0161] (Charge transport layer 1) A coating solution for the charge transport layer was prepared by dissolving 60 parts of the compound represented by formula (F) below, 30 parts of the compound represented by formula (G) below, 10 parts of the compound represented by formula (H) below, 100 parts of bisphenol Z type polycarbonate resin (product name: Yupiron Z400, manufactured by Mitsubishi Engineering Plastics Corporation), and 0.2 parts of polycarbonate having the unit represented by formula (I) below (viscosity-average molecular weight Mv: 20000) in a mixed solvent of 272 parts o-xylene, 256 parts methyl benzoate, and 272 parts dimethoxymethane. This charge transport layer coating solution was applied to the charge generating layer 1 by immersion to form a coating film, and the resulting coating film was dried at 115°C for 50 minutes to form a charge transport layer 1 with a thickness of 18 μm. [ka] (In equation (I), 0.95 and 0.05 are the molar ratios (copolymerization ratios) of the two units.)

[0162] (Protective layer 1) A dispersant solution was prepared by dissolving 2.20 parts of the aforementioned graft copolymer 1 in a mixed solvent consisting of 100 parts of 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl ether (trade name: AE-3000, manufactured by AGC Inc.) and 100 parts of 1-propanol. 40 parts of polytetrafluoroethylene resin particles (average primary particle size 210 nm, average roundness 0.85) were added to the obtained dispersant solution. Then, the mixture was passed through a high-pressure disperser (product name: Microfluidizer M-110EH, manufactured by Microfluidics, Inc., USA) to obtain a polytetrafluoroethylene resin particle dispersion. To the obtained polytetrafluoroethylene resin particle dispersion, 75.4 parts of a hole-transporting compound represented by formula (K) below, 21.9 parts of a compound represented by formula (D) below, and 100 parts of 1-propanol were added. Subsequently, the mixture was filtered using a polyflon filter (product name: PF-040, manufactured by Advantec Toyo Co., Ltd.) to prepare a polytetrafluoroethylene resin particle dispersion (coating solution for protective layer). [ka] [ka]

[0163] The protective coating solution was applied to the charge transport layer by immersion to form a coating film, and the resulting coating film was dried at 40°C for 5 minutes. After drying, the coating film was irradiated with an electron beam for 1.6 seconds under conditions of an accelerating voltage of 70kV and an absorbed dose of 15kGy in a nitrogen atmosphere. Subsequently, a heat treatment was performed for 15 seconds under conditions of a nitrogen atmosphere to bring the temperature of the coating film to 135°C. The oxygen concentration from electron beam irradiation to the 15-second heat treatment was 15ppm. Next, the coating film was allowed to cool naturally in air until its temperature reached 25°C, and then a heat treatment was performed for 1 hour to bring the temperature of the coating film to 105°C to form a surface layer (protective layer 1) with a thickness of 5μm. The content of 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl ether in the surface layer was 5 ppm. In this way, an electrophotographic photoreceptor having a support and a surface layer before surface polishing was produced.

[0164] <Surface Processing of Electrophotographic Photoreceptor> (Polishing of Electrophotographic Photoreceptor before Surface Polishing) The surface of the electrophotographic photoreceptor before forming the surface shape was polished. The polishing was carried out using the polishing apparatus shown in Fig. 2 under the following conditions. Feed speed of polishing sheet: 400 mm / min Rotation speed of electrophotographic photoreceptor: 450 rpm Pushing-in of electrophotographic photoreceptor to backup roller: 3.5 mm Rotation direction of polishing sheet and electrophotographic photoreceptor: with Backup roller: outer diameter 100 mm, Asker C hardness 25 The polishing sheet A to be mounted on the polishing apparatus was prepared by mixing the polishing abrasive grains used for GC3000 and GC2000 manufactured by Riken Korundum Co., Ltd. GC3000 (polishing sheet surface roughness Ra 0.83 μm) GC2000 (polishing sheet surface roughness Ra 1.45 μm) Polishing sheet A (polishing sheet surface roughness Ra 1.12 μm) The polishing time using polishing sheet A was set to 20 seconds.

[0165] (Measurement of Polishing Depth L (μm)) For the electrophotographic photoreceptor after polishing, the maximum height Rmax in accordance with JIS B 0601 1982 was measured using a surface roughness measuring instrument Surfcoader SE3500 type manufactured by Kosaka Laboratory Ltd. The measurement conditions were set as follows. The measurement was carried out arbitrarily at three places in a 5 mm square range of the electrophotographic photoreceptor after polishing, and the average value was adopted as the polishing depth L (μm). The polishing depth L of the electrophotographic photoreceptor after surface polishing was 0.75 μm. Also, in Examples 1-2 to 1-27 and Comparative Examples 1-1 to 1-5 described later, the polishing depth L of the electrophotographic photoreceptor subjected to surface processing was all 0.75 μm. (Measurement Conditions) Detector: R2μm Stylus: diamond needle of 0.7 mN Filter: 2CR Cutoff value: 0.08mm Measurement length: 2.5mm Feed speed: 0.1mm

[0166] [Examples 1-2 to 1-5] An electrophotographic photoreceptor was prepared in the same manner as in Example 1-1, except that the protective layer was formed using polytetrafluoroethylene particles with the average primary particle size and average roundness shown in Table 4. The content of 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl ether in the surface layer is shown in Table 4.

[0167] [Examples 1-6 to 1-9] An electrophotographic photoreceptor was prepared in the same manner as in Example 1-1, except that the graft copolymer 1 was changed to the parts by mass shown in Table 4 during the formation of the protective layer. The content of 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl ether in the surface layer is shown in Table 4.

[0168] [Examples 1-10 to 1-24, Examples 1-26 to 1-27, Comparative Examples 1-1 to 1-5] An electrophotographic photoreceptor was prepared in the same manner as in Example 1-1, except that graft copolymer 1 was changed to the graft copolymer shown in Table 4 during the formation of the protective layer. The content of 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl ether in the surface layer is shown in Table 4.

[0169] [Examples 1-25] An electrophotographic photoreceptor was prepared in the same manner as in Example 1-1, except that the protective layer coating solution was prepared under the following conditions. A dispersant solution was prepared by dissolving 2.2 parts of graft copolymer 1 in 80 parts of tetrahydrofuran as a solvent. 31 parts of polytetrafluoroethylene resin particles (average primary particle size 210 nm, average roundness 0.85) were added to the obtained dispersant solution. The solution was then passed through a high-pressure disperser (product name: Microfluidizer M-110EH, manufactured by Microfluidics, Inc., USA) to obtain a polytetrafluoroethylene resin particle dispersion. To the obtained polytetrafluoroethylene resin particle dispersion, 161 parts of the charge transport compound represented by formula C-26, 5 parts of the guanamine compound represented by formula (J), 2.6 parts of 3,5-di-t-butyl-4-hydroxytoluene (BHT), 0.4 parts of dodecylbenzenesulfonic acid, and 130 parts of cyclopentanone and 90 parts of cyclopentanol were added. The mixture was then filtered using a polyflon filter (product name: PF-040, manufactured by Advantec Toyo Co., Ltd.) to obtain the protective coating solution for Example 1-25. [ka]

[0170] [Table 4]

[0171] <Evaluation of electrophotographic photoconductors> The electrophotographic photoreceptors obtained in Examples 1-1 to 1-27 and Comparative Examples 1-1 to 1-5 were evaluated as follows.

[0172] [Evaluation device 1-1] The electrophotographic photoreceptors prepared in Examples 1-1 to 1-27 and Comparative Examples 1-1 to 1-5 were mounted in a Canon imagePRESS C800 copier (product name) and evaluated. In detail, the evaluation apparatus was set up in a high-temperature, high-humidity environment of 30°C and 80% RH relative humidity. The fabricated electrophotographic photoreceptor was mounted onto a magenta process cartridge, which was then mounted on the magenta process cartridge station for evaluation.

[0173] [Evaluation device 1-2] The electrophotographic photoreceptors prepared in Examples 1-1 to 1-27 and Comparative Examples 1-1 to 1-5 were installed in a modified Canon imagePRESS C800 copier (product name) and evaluated. The charging means of the modified copier is a method of applying a voltage obtained by superimposing an AC voltage on a DC voltage to a roller-type contact charging member (charging roller), and the exposure means is a laser image exposure method (wavelength 680 nm). In detail, the evaluation apparatus was set up in a high-temperature, high-humidity environment of 30°C and 80% RH relative humidity. The fabricated electrophotographic photoreceptor was mounted onto a magenta process cartridge, which was then mounted on the magenta process cartridge station for evaluation. The charging conditions were adjusted so that the charging potential was -800V and the exposure potential was -300V, by adjusting the charging potential and the exposure amount of the exposure means. The surface potential of the electrophotographic photoreceptor was measured by removing the developing cartridge from the evaluation apparatus described above, inserting a potential measuring device into its place, and then measuring the potential. The potential measuring device consists of a potential measuring probe (product name: model6000B-8, manufactured by Trek Japan Co., Ltd.) placed at the developing position of the developing cartridge. The position of the potential measuring probe relative to the electrophotographic photoreceptor was set to the center in the direction of the electrograph line of the electrophotographic photoreceptor, with a gap of 3 mm from the surface of the electrophotographic photoreceptor. Furthermore, the potential of the central part of the electrophotographic photoreceptor was measured using a surface potential meter (product name: model344, manufactured by Trek Japan Co., Ltd.).

[0174] (Initial image evaluation) Image evaluation was performed using the evaluation apparatus 1-1 described above. Using A4 size gloss paper, a completely white image was output, and the number of image defects due to dispersion defects, i.e., black dots, contained in the area of ​​one circumference of the electrophotographic photoreceptor in the output image was visually evaluated. The number of black dots with a diameter of 0.3 mm or more was evaluated. The area of ​​one circumference of the electrophotographic photoreceptor is a rectangular area with a vertical dimension of 297 mm (the length of the long side of the A4 paper) and a horizontal dimension of 96.1 mm (the circumference of one circumference of the electrophotographic photoreceptor). In this disclosure, a smaller number of black dots is better, and the effects of this disclosure are achieved. The results of this evaluation are shown in Table 5.

[0175] (Evaluation of potential fluctuations during repeated use) The potential fluctuation evaluation during repeated use was performed using the evaluation device 1-2 described above. A cartridge equipped with an electrophotographic photoreceptor was attached to the evaluation device, and the photoreceptor was repeatedly used by feeding 100,000 sheets of paper. At the station where the electrophotographic photoreceptor was installed, 100,000 images of a single-color character image with a print density of 1% were repeatedly formed on A4 size plain paper. The initial dark area potential at this time was compared with the dark area potential after 100,000 repeated image formations, and this was defined as the potential fluctuation value (ΔVd). Similarly, the initial bright area potential was compared with the bright area potential after 100,000 repeated image formations, and this was defined as the potential fluctuation value (ΔVl). After feeding 100,000 sheets of paper, it was left for 5 minutes, and the developing cartridge was replaced with a potential measuring device, and the bright area potential (Vlb) and dark area potential (Vdb) after repeated use were measured. The difference between the dark area potential after repeated use and the initial dark area potential (Vda) was defined as the dark area potential fluctuation (ΔVd = |Vdb| - |Vda|). Similarly, the difference between the bright area potential after repeated use and the initial bright area potential (Vla) was defined as the bright area potential fluctuation (ΔVl = |Vlb| - |Vla|). In this disclosure, the smaller the change in the potential of the bright area, the better, and the effects of this disclosure are obtained. The results of this evaluation are shown in Table 5.

[0176] [Table 5]

[0177] [Example 2-1] (Support 2) As the support (conductive support), a cylindrical aluminum cylinder (JIS-A3003, aluminum alloy, outer diameter 30 mm, length 357.5 mm, wall thickness 0.7 mm) was machined and used. Ultrasonic cleaning was performed in a cleaning solution containing detergent (product name: Chemicol CT, manufactured by Tokiwa Chemical Co., Ltd.) in pure water, followed by rinsing off the cleaning solution, and then further ultrasonic cleaning in pure water to degrease it, which was then used as support 2.

[0178] (Bottom layer 2) Sixty parts of zinc oxide particles (average particle size: 70 nm, specific surface area: 15 m² / g) were mixed with 500 parts of tetrahydrofuran by stirring. 0.75 parts of a silane coupling agent (compound name: N-2-(aminoethyl)-3-aminopropyltrimethoxysilane, trade name: KBM603, manufactured by Shin-Etsu Chemical Co., Ltd.) were added, and the mixture was stirred for 2 hours. Subsequently, the tetrahydrofuran was removed by distillation under reduced pressure, and the mixture was heated and dried at 120°C for 3 hours to obtain surface-treated zinc oxide particles.

[0179] Next, 25 parts of butyral (product name: BM-1, manufactured by Sekisui Chemical Co., Ltd.) and 22.5 parts of blocked isocyanate (product name: Sumijool BL-3173, manufactured by Sumitomo Bayer Urethane Co., Ltd.) were dissolved in 142 parts of methyl ethyl ketone. To this solution, 100 parts of the surface-treated zinc oxide particles and 1 part of anthraquinone were added, and the mixture was dispersed for 5 hours using glass beads with a diameter of 1 mm in a sand mill. After dispersion treatment, 0.008 parts of dioctyltin dilaurate and 6.5 parts of silicone resin particles (Tospar 145, manufactured by GE Toshiba Silicone Co., Ltd.) were added and stirred to prepare a coating solution for the undercoat layer. The obtained undercoating solution for the undercoat layer was applied to the support by immersion to form a coating film, and the coating film was dried at 190°C for 24 minutes to form an undercoat layer 2 with a thickness of 15 μm.

[0180] (Charge generation layer 2) Next, 15 parts of chlorogallium phthalocyanine crystals having strong diffraction peaks at Bragg angles (2θ±0.2°) of at least 7.4°, 16.6°, 25.5°, and 28.3° relative to CuKα characteristic X-rays, 10 parts of vinyl chloride-vinyl acetate copolymer resin (VMCH, manufactured by Union Carbide Japan Co., Ltd.), and 300 parts of n-butyl alcohol were mixed and dispersed for 4 hours using a sand mill with glass beads with a diameter of 1 mm to prepare a coating solution for the charge generation layer. This charge generation layer coating solution was applied to the undercoat layer by immersion, and the resulting coating film was dried at 150°C for 5 minutes to form a charge generation layer 2 with a thickness of 0.2 μm.

[0181] (Charge transport layer 2) Next, 20 parts of polytetrafluoroethylene resin particles (average primary particle size 210 nm, average roundness 0.85), 2.20 parts of the aforementioned graft copolymer 1, and 24 parts of tetrahydrofuran were stirred and mixed for 48 hours while maintaining a liquid temperature of 20°C to obtain preparation A.

[0182] Next, 53.2 parts of N,N'-bis(3-methylphenyl)-N,N'-diphenylbenzicine, 14.1 parts of bisphenol Z-type polycarbonate resin (viscosity average molecular weight 40,000), and 0.26 parts of 2,6-di-t-butyl-4-methylphenol as an antioxidant were mixed, and 250 parts of tetrahydrofuran were mixed and dissolved to obtain preparation B.

[0183] After adding preparation A to preparation B and stirring, the mixture was passed through a high-pressure disperser (product name: Microfluidizer M-110EH, manufactured by Microfluidics, Inc., USA) to obtain a dispersion. Subsequently, fluorine-modified silicone oil (product name: FL-100, manufactured by Shin-Etsu Silicone Co., Ltd.) was added to the dispersion to a concentration of 5 ppm, and the mixture was filtered using a polyflon filter (product name: PF-040, manufactured by Advantec Toyo Co., Ltd.) to prepare a coating solution for the charge transport layer. This charge transport layer coating solution was applied to the charge generation layer by immersion to form a coating film, and the resulting coating film was dried at 150°C for 25 minutes to form a charge transport layer 2 with a thickness of 33 μm. In this way, an electrophotographic photoreceptor was fabricated in which the charge transport layer is the surface layer.

[0184] [Examples 2-2 to 2-5] An electrophotographic photoreceptor was fabricated in the same manner as in Example 2-1, except that the charge transport layer 2 was formed using polytetrafluoroethylene particles with the average primary particle size and average roundness shown in Table 6.

[0185] [Examples 2-6 to 2-9] An electrophotographic photoreceptor was fabricated in the same manner as in Example 2-1, except that the graft copolymer 1 was changed to the part by mass shown in Table 6 during the formation of the charge transport layer 2.

[0186] [Examples 2-10 to 2-26, Comparative Examples 2-1 to 2-5] An electrophotographic photoreceptor was fabricated in the same manner as in Example 2-1, except that the graft copolymer 1 was changed to the graft copolymer shown in Table 6 during the formation of the charge transport layer 2.

[0187] [Table 6]

[0188] <Evaluation of electrophotographic photoconductors> The electrophotographic photoreceptors obtained in Examples 2-1 to 2-26 and Comparative Examples 2-1 to 2-5 were evaluated as follows.

[0189] [Evaluation device 2-1] The electrophotographic photoreceptors prepared in Examples 2-1 to 2-26 and Comparative Examples 2-1 to 2-5 were installed in a Canon imageRUNNER ADVANCE DX C3835F (product name) copier and evaluated. In detail, the evaluation apparatus was set up in a high-temperature, high-humidity environment of 30°C and 80% RH relative humidity. The fabricated electrophotographic photoreceptor was mounted onto a magenta process cartridge, which was then mounted on the magenta process cartridge station for evaluation.

[0190] [Evaluation device 2-2] The electrophotographic photoreceptors prepared in Examples 2-1 to 2-26 and Comparative Examples 2-1 to 2-5 were evaluated by mounting them in a modified Canon imageRUNNER ADVANCE DX C3835F (product name) copier (the charging method uses a DC voltage applied to a roller-type contact charging element (charging roller), and the exposure method is a laser image exposure method (wavelength 780 nm)). Specifically, the evaluation apparatus was set up in a high-temperature, high-humidity environment of 30°C and 80% RH, and the electrophotographic photoreceptors prepared in the magenta process cartridges were mounted and then placed in the magenta process cartridge station for evaluation. The surface potential of the electrophotographic photoreceptor was measured by removing the developing cartridge from the evaluation apparatus described above and inserting a potential measuring device into it. The potential measuring device consisted of a potential measuring probe (product name: model6000B-8, manufactured by Trek Japan Co., Ltd.) placed at the developing position of the developing cartridge. The position of the potential measuring probe relative to the electrophotographic photoreceptor was set to the center in the direction of the electrograph line of the electrophotographic photoreceptor, with a gap of 3 mm from the surface of the electrophotographic photoreceptor. Furthermore, the potential of the central part of the electrophotographic photoreceptor was measured using a surface potential meter (product name: model344, manufactured by Trek Japan Co., Ltd.).

[0191] (Initial image evaluation) Image evaluation was performed using the evaluation apparatus 2-1 described above. Using A4 size gloss paper, a completely white image was output, and the number of image defects due to dispersion defects, i.e., black dots, contained in the area of ​​one circumference of the electrophotographic photoreceptor in the output image was visually evaluated. The number of black dots with a diameter of 0.3 mm or more was evaluated. The area of ​​one circumference of the electrophotographic photoreceptor is a rectangular area with a vertical dimension of 297 mm (the length of the long side of the A4 paper) and a horizontal dimension of 96.1 mm (the circumference of one circumference of the electrophotographic photoreceptor). In this disclosure, a smaller number of black dots is better, and the effects of this disclosure are achieved. The results of this evaluation are shown in Table 7.

[0192] (Evaluation of potential fluctuations during repeated use) The potential fluctuation evaluation during repeated use was performed using the evaluation device 2-2 described above. A cartridge equipped with an electrophotographic photoreceptor was attached to the evaluation device, and the photoreceptor was repeatedly used by feeding 50,000 sheets of paper. At the station where the electrophotographic photoreceptor was installed, 50,000 images of a single-color character image with a print density of 1% were repeatedly formed on A4 size plain paper. The initial dark area potential at this time was compared with the dark area potential after 50,000 repeated image formations, and this was defined as the potential fluctuation value (ΔVd). Similarly, the initial bright area potential was compared with the bright area potential after 50,000 repeated image formations, and this was defined as the potential fluctuation value (ΔVl). After feeding 50,000 sheets of paper, it was left for 5 minutes, and the developing cartridge was replaced with a potential measuring device, and the bright area potential (Vlb) and dark area potential (Vdb) after repeated use were measured. The difference between the dark area potential after repeated use and the initial dark area potential (Vda) was defined as the dark area potential fluctuation (ΔVd = |Vdb| - |Vda|). Similarly, the difference between the bright area potential after repeated use and the initial bright area potential (Vla) was defined as the bright area potential fluctuation (ΔVl = |Vlb| - |Vla|). In this disclosure, the smaller the change in the potential of the bright area, the better, and the effects of this disclosure are obtained. The results of this evaluation are shown in Table 7.

[0193] [Table 7] [Explanation of Symbols]

[0194] 101 Base 102 Lower layer 103 Charge generation layer 104 Charge transport layer 105 Surface layer 1. Electrophotographic photoreceptor 2. Charging means 3. Exposure light (image exposure light) 4. Developing means 5. Transfer means 6 Transfer material 7. Pre-exposure light 8. Cleaning methods 9 Process Cartridges 10 Intermediate Transfer 11 Transfer paper 12 Paper feed path 13 Paper feed tray 14. Secondary transfer means 15 Fixing means 16 Paper output section 17 Process cartridge for yellow color 18 Magenta Process Cartridges 19 Cyan process cartridge 20 Process cartridges for black color

Claims

1. An electrophotographic photoreceptor having a surface layer, The surface layer is Fluorine atom-containing resin particles, Binding material and, Polymer A having structural units represented by the following formula (1) and structural units represented by the following formula (2), Contains An electrophotographic photoreceptor characterized by the following features. 【Chemistry 1】 (In formula (1), R １１ This represents a hydrogen atom or a methyl group. R １２ This represents a single bond, a methylene group, or an ethylene group. Rf １ This represents a perfluoroalkylene group having 1 to 5 carbon atoms, or a perfluoroalkylidene group having 1 to 5 carbon atoms. Rf ２ This represents a perfluoroalkyl group having 1 to 5 carbon atoms. Rf １ and Rf ２ The total number of carbon atoms is 6 or more. 【Chemistry 2】 (In formula (2), Y Ａ１ This shows an unsubstituted alkylene group, Y Ｂ This represents an unsubstituted alkylene group, a halogen-substituted alkylene group, a hydroxyl-substituted alkylene group, an ester bond (-COO-), an amide bond (-NHCO-), or a urethane bond (-NHCOO-), or a divalent linking group that can be derived by combining one or more of these groups and bonds with -O- or -S-, or a single bond. Z Ａ represents a structure represented by the following formula (2A), a cyano group, or a phenyl group, R ２１ , and R ２２ This represents a hydrogen atom or a methyl group. m is an integer between 25 and 150. 【Transformation 3】 (In formula (2A), Z Ａ１ (This represents an alkyl group having 1 to 4 carbon atoms.)

2. The electrophotographic photoreceptor according to claim 1, wherein polymer A does not have structural units having acidic groups with a pKa of 3 or less.

3. The electrophotographic photoreceptor according to claim 1 or 2, wherein the polymer A has only the structural unit represented by formula (1) and the structural unit represented by formula (2) as structural units.

4. Rf in equation (1) １ and Rf ２ The electrophotographic photoreceptor according to any one of claims 1 to 3, wherein the total number of carbon atoms is 6 or more and 9 or less.

5. The electrophotographic photoreceptor according to any one of claims 1 to 4, wherein the weight-average molecular weight of polymer A is 16,000 or more and 100,000 or less.

6. The electrophotographic photoreceptor according to any one of claims 1 to 5, wherein the content of polymer A in the surface layer is 2% by mass or more and 10% by mass or less relative to the content of fluorine atom-containing resin particles in the surface layer.

7. The electrophotographic photoreceptor according to any one of claims 1 to 6, wherein the content of the fluorine atom-containing resin particles in the surface layer is 5% by mass or more and 40% by mass or less with respect to the total mass of the surface layer.

8. The electrophotographic photoreceptor according to any one of claims 1 to 7, wherein the fluorine atom-containing resin particles are polytetrafluoroethylene resin particles.

9. The electrophotographic photoreceptor according to any one of claims 1 to 8, wherein the arithmetic mean of the major axis of the primary particles of the fluorine atom-containing resin particles is 150 nm or more and 300 nm or less.

10. The electrophotographic photoreceptor according to any one of claims 1 to 9, wherein the binder is a cured product of a hole-transporting compound having polymerizable functional groups.

11. The electrophotographic photoreceptor according to claim 10, wherein the hole transporting compound having the polymerizable functional group is a compound represented by the following formula (CT-1) or (CT-2). 【Chemistry 4】 (In formula (CT-1), Ar １１ ~Ar １３ Each of these independently represents either a substituted aryl group or an unsubstituted aryl group. The substituents that the substituted aryl group may have are alkyl groups having 1 to 6 carbon atoms, or monovalent functional groups represented by any of the following formulas (P-1) to (P-3). However, the compound represented by formula (CT-1) has at least one monovalent functional group represented by any of the following formulas (P-1) to (P-3). 【Transformation 5】 (In formula (CT-2), Ar ２１ ~Ar ２４ Each of these independently represents a substituted aryl group or an unsubstituted aryl group, Ar ２５ This represents a substituted aryl group or an unsubstituted aryl group. The substituents that the substituted aryl group may have are alkyl groups having 1 to 6 carbon atoms, or monovalent functional groups represented by the following formulas (P-1) to (P-3). The substituents that the substituted aryl group may have are alkyl groups having 1 to 6 carbon atoms, or monovalent functional groups represented by the following formulas (P-1) to (P-3). However, the compound represented by formula (CT-2) has at least one monovalent functional group represented by any of the following formulas (P-1) to (P-3). 【Transformation 6】 (In formula (P-1), Z １１ X represents a single bond or an alkylene group having 1 to 6 carbon atoms. １１ (This represents a hydrogen atom or a methyl group.) 【Transformation 7】 (In formula (P-2), Z ２１ (This represents a single bond or an alkylene group having 1 to 6 carbon atoms.) 【Transformation 8】 (In formula (P-3), Z ３１ (This represents a single bond or an alkylene group having 1 to 6 carbon atoms.)

12. The electrophotographic photoreceptor according to claim 10 or 11, wherein the content of the fluorine atom-containing resin particles in the surface layer is 20% by mass or more and 40% by mass or less with respect to the total mass of the surface layer.

13. The aforementioned binding material is Charge transport compounds and At least one triazine compound selected from the group consisting of guanamine compounds and melamine compounds, hardened product An electrophotographic photoreceptor according to any one of claims 1 to 12, comprising the above.

14. The electrophotographic photoreceptor according to claim 13, wherein the charge transporting compound has at least one polymerizable functional group selected from a methylol group and a methoxy group.

15. The electrophotographic photoreceptor according to claim 13 or 14, wherein the content of the fluorine atom-containing resin particles in the surface layer is 5% by mass or more and 15% by mass or less with respect to the total mass of the surface layer.

16. The aforementioned binding material includes a thermoplastic resin, The surface layer further contains a charge transport material, The thermoplastic resin is at least one resin selected from polycarbonate resin and polyarylate resin. The electrophotographic photoreceptor according to any one of claims 1 to 15.

17. The electrophotographic photoreceptor according to claim 16, wherein the charge transport material is at least one selected from the group consisting of compounds represented by the following formula (3) and compounds represented by the following formula (4). 【Chemistry 9】 (In formula (3), R Ｃ２１ , R Ｃ２２ and R Ｃ２３ Each of these independently represents a hydrogen atom, a halogen atom, an alkyl group having 1 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, or an aryl group having 6 to 10 carbon atoms. 【Chemistry 10】 (In formula (4), R Ｃ１１ , R Ｃ１２ , R Ｃ１３ , R Ｃ１４ , R Ｃ１５ , and R Ｃ１６ Each of these independently represents a hydrogen atom, a halogen atom, an alkyl group having 1 to 20 carbon atoms, an alkoxy group having 1 to 20 carbon atoms, or an aryl group having 6 to 30 carbon atoms, and two adjacent substituents may be bonded together to form a hydrocarbon ring structure, and m and n are each independently 0, 1, or 2.

18. The electrophotographic photoreceptor according to claim 16 or 17, wherein the content of the fluorine atom-containing resin particles in the surface layer is 5% by mass or more and 15% by mass or less with respect to the total mass of the surface layer.

19. A process cartridge characterized by integrally supporting an electrophotographic photoreceptor according to any one of claims 1 to 18 and at least one means selected from the group consisting of a charging means, a developing means, a transfer means, a static elimination means and a cleaning means, and being detachable from the main body of an electrophotographic apparatus.

20. An electrophotographic apparatus characterized by comprising an electrophotographic photoreceptor according to any one of claims 1 to 18, and a charging means, an exposure means, a developing means, and a transfer means.

21. A method for manufacturing an electrophotographic photoreceptor having a surface layer, The manufacturing method is A step of preparing a coating solution for a surface layer containing polymer A having structural units represented by the following formula (1) and structural units represented by the following formula (2), fluorine atom-containing resin particles, and at least one selected from a binder and a raw material for the binder, and The process includes the step of forming a coating film of the surface layer coating liquid, and then drying and / or curing the coating film to form the surface layer. A method for manufacturing an electrophotographic photoreceptor, characterized by the above. 【Chemistry 11】 (In formula (1), R １１ This represents a hydrogen atom or a methyl group. R １２ This represents a single bond, a methylene group, or an ethylene group. Rf １ This represents a perfluoroalkylene group having 1 to 5 carbon atoms, or a perfluoroalkylidene group having 1 to 5 carbon atoms. Rf ２ This represents a perfluoroalkyl group having 1 to 5 carbon atoms. The sum of the number of carbon atoms in Rf 1 and Rf 2 is 6 or more. 【Chemistry 12】 (In formula (2), Y Ａ１ This shows an unsubstituted alkylene group, Y Ｂ This represents an unsubstituted alkylene group, a halogen-substituted alkylene group, a hydroxyl-substituted alkylene group, an ester bond (-COO-), an amide bond (-NHCO-), or a urethane bond (-NHCOO-), or a divalent linking group that can be derived by combining one or more of these groups and bonds with -O- or -S-, or a single bond. Z Ａ This refers to the structure represented by the following formula (2A), a cyano group, or a phenyl group. R ２１ , and R ２２ This represents a hydrogen atom or a methyl group. m is an integer between 25 and 150. 【Chemistry 13】 (In formula (2A), Z Ａ１ (This represents an alkyl group having 1 to 4 carbon atoms.)

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