JP6558327B2 - Electrophotographic photosensitive member, process cartridge, image forming apparatus, and image forming method - Google Patents

Description

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

  The electrophotographic photosensitive member is used in an electrophotographic image forming apparatus. The electrophotographic photoreceptor includes a photosensitive layer. In one example of the electrophotographic photosensitive member, the electrophotographic photosensitive member includes a single photosensitive layer having a charge generation function and a charge transport function. The multilayer photosensitive device described in Patent Document 1 contains a compound represented by the chemical formula (ETM-A) as an electron transport material.

JP 60-69657 A

  However, in an electrophotographic photoreceptor in which a compound represented by the chemical formula (ETM-A) is contained in the photosensitive layer, it is difficult to improve filming resistance and suppress the generation of transfer memory.

  The present invention has been made in view of the above-described problems, and an object of the present invention is to provide an electrophotographic photosensitive member capable of improving filming resistance and suppressing generation of a transfer memory. Another object of the present invention is to provide a process cartridge and an image forming apparatus that can improve filming resistance and suppress the generation of a transfer memory by including such an electrophotographic photosensitive member. Furthermore, an object of the present invention is to provide an image forming method capable of forming a good image by using an electrophotographic photosensitive member capable of improving filming resistance and suppressing generation of a transfer memory.

  The electrophotographic photoreceptor of the present invention includes a conductive substrate and a photosensitive layer. The photosensitive layer is a single layer. The photosensitive layer includes a charge generating agent, a hole transport agent, an electron transport agent, a binder resin, and filler particles. The filler particles are at least one of silica particles and resin particles. The electron transfer agent includes at least one compound represented by the general formula (1).

In the general formula (1), R ₁ is an alkyl group having 1 to 8 carbon atoms having one or more halogen atoms, a cycloalkyl group having 3 to 10 carbon atoms having one or more halogen atoms, halogen An aryl group having 6 to 14 carbon atoms which may have an alkyl group having 1 or more atoms and having 1 to 6 carbon atoms, or a 5- to 14-membered heterocyclic ring having one or more halogen atoms A group or an aralkyl group having 7 or more and 20 or less carbon atoms having at least one halogen atom;

  The process cartridge of the present invention includes the above-described electrophotographic photosensitive member.

  An image forming apparatus of the present invention includes the above-described electrophotographic photosensitive member, a charging unit, an exposure unit, a developing unit, and a transfer unit. The charging unit charges the surface of the electrophotographic photosensitive member to a positive polarity. The exposure unit exposes the charged surface of the electrophotographic photosensitive member to form an electrostatic latent image on the surface of the electrophotographic photosensitive member. The developing unit supplies toner to the electrostatic latent image and develops the electrostatic latent image as a toner image. The transfer unit transfers the toner image from the electrophotographic photosensitive member to a transfer target.

  The image forming method of the present invention includes a charging step, an exposure step, a development step, and a transfer step. In the charging step, the surface of the electrophotographic photosensitive member is charged to a positive polarity. In the exposure step, the charged surface of the electrophotographic photosensitive member is exposed to form an electrostatic latent image on the surface of the electrophotographic photosensitive member. In the developing step, polymerized toner is supplied to the electrostatic latent image, and the electrostatic latent image is developed as a toner image. In the transfer step, the toner image is transferred from the electrophotographic photosensitive member to the transfer target.

  According to the electrophotographic photosensitive member of the present invention, the filming resistance can be improved and the generation of a transfer memory can be suppressed. In addition, according to the process cartridge and the image forming apparatus of the present invention, by providing such an electrophotographic photosensitive member, it is possible to improve the filming resistance and to suppress the generation of a transfer memory. Furthermore, according to the image forming method of the present invention, by using such an electrophotographic photoreceptor, it is possible to form a good image while suppressing the occurrence of filming and the generation of a transfer memory.

(A), (b) and (c) are sectional views showing an example of an electrophotographic photoreceptor according to an embodiment of the present invention. It is an example of a CuKα characteristic X-ray diffraction spectrum chart of titanyl phthalocyanine, and this titanyl phthalocyanine is used in the electrophotographic photoreceptor according to the embodiment of the present invention. 1 is a diagram illustrating an example of a configuration of an image forming apparatus, and the image forming apparatus includes an electrophotographic photosensitive member according to an embodiment of the present invention. ¹ is a ¹ H-NMR spectrum of a compound represented by the chemical formula (1-3), and this compound is used in an electrophotographic photoreceptor according to an embodiment of the present invention. ¹ is a ¹ H-NMR spectrum of a compound represented by the chemical formula (1-4), and this compound is used in an electrophotographic photoreceptor according to an embodiment of the present invention. It is a figure which shows the image for evaluation. It is a figure which shows the image which image ghost generate | occur | produced.

  Hereinafter, embodiments of the present invention will be described in detail. However, the present invention is not limited to the following embodiments. The present invention can be implemented with appropriate modifications within the scope of the object of the present invention. In addition, about the location where description overlaps, although description may be abbreviate | omitted suitably, the summary of invention is not limited.

  Hereinafter, a compound and its derivatives may be generically named by adding “system” after the compound name. In addition, when “polymer” is added after the compound name to indicate the polymer name, it means that the repeating unit of the polymer is derived from the compound or a derivative thereof. Furthermore, the reactions represented by the reaction formulas (R-1) to (R-4), (R-A) and (R-B) are respectively represented by reactions (R-1) to (R-4), (R -A) and (RB) may be described.

  Hereinafter, a halogen atom, an alkyl group having 1 to 8 carbon atoms, an alkyl group having 1 to 6 carbon atoms, an alkyl group having 1 to 4 carbon atoms, an alkyl group having 1 to 3 carbon atoms, carbon An alkyl group having 3 to 5 atoms, an alkoxy group having 1 to 6 carbon atoms, an aryl group having 6 to 14 carbon atoms, a cycloalkane having 5 to 7 carbon atoms, a cycloalkylidene group, and the number of carbon atoms 5 to 7 or less cycloalkylidene group, 5 to 14 membered heterocyclic group, 5 or 6 membered heterocyclic group, cycloalkyl group having 3 to 10 carbon atoms, and 7 to 20 carbon atoms Aralkyl groups have the following meanings unless otherwise specified.

  The halogen atom (halogen group) is, for example, a fluorine atom (fluoro group), a chlorine atom (chloro group), a bromine atom (bromo group), or an iodine atom (iodo group).

  The alkyl group having 1 to 8 carbon atoms is linear or branched and unsubstituted. Examples of the alkyl group having 1 to 8 carbon atoms include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, n-pentyl group, isopentyl group. Group, neopentyl group, 1,2-dimethylpropyl group, hexyl group, heptyl group or octyl group. Examples of the alkyl group having 1 to 6 carbon atoms are groups having 1 to 6 carbon atoms among the groups described as examples of alkyl groups having 1 to 8 carbon atoms. Examples of the alkyl group having 1 to 4 carbon atoms are groups having 1 to 4 carbon atoms among the groups described as examples of alkyl groups having 1 to 8 carbon atoms. Examples of the alkyl group having 1 to 3 carbon atoms are groups having 1 to 3 carbon atoms among the groups described as examples of alkyl groups having 1 to 8 carbon atoms. Examples of the alkyl group having 3 to 5 carbon atoms are groups having 3 to 5 carbon atoms among the groups described as examples of alkyl groups having 1 to 8 carbon atoms.

  The alkoxy group having 1 to 6 carbon atoms is linear or branched and unsubstituted. Examples of the alkoxy group having 1 to 6 carbon atoms include methoxy group, ethoxy group, n-propoxy group, isopropoxy group, n-butoxy group, sec-butoxy group, tert-butoxy group, n-pentoxy group, An isopentoxy group, a neopentoxy group, or a hexyl group may be mentioned.

  Examples of the aryl group having 6 to 14 carbon atoms include an unsubstituted aromatic monocyclic hydrocarbon group having 6 to 14 carbon atoms and an unsubstituted aromatic condensed bicyclic carbon group having 6 to 14 carbon atoms. A hydrogen group or an unsubstituted aromatic condensed tricyclic hydrocarbon group having 6 to 14 elemental atoms. Examples of the aryl group having 6 to 14 carbon atoms include a phenyl group, a naphthyl group, an anthryl group, and a phenanthryl group.

  A cycloalkane having 5 to 7 carbon atoms is unsubstituted. Examples of the cycloalkane having 5 to 7 carbon atoms include cyclopentane, cyclohexane, and cycloheptane.

  A cycloalkylidene group is unsubstituted. An example of the cycloalkylidene group is a cycloalkylidene group having 5 to 7 carbon atoms. A cycloalkylidene group having 5 to 7 carbon atoms is unsubstituted. Examples of the cycloalkylidene group having 5 to 7 carbon atoms include a cyclopentylidene group, a cyclohexylidene group, and a cycloheptylidene group.

  The 5- to 14-membered heterocyclic group contains at least one heteroatom in addition to the carbon atom and is unsubstituted. The hetero atom is at least one selected from the group consisting of a nitrogen atom, a sulfur atom and an oxygen atom. The 5- to 14-membered heterocyclic group includes, for example, a 5-membered or 6-membered monocyclic heterocyclic group containing 1 to 3 heteroatoms in addition to the carbon atom; A heterocyclic group in which two monocyclic rings are fused; a heterocyclic group in which such a monocyclic heterocyclic ring is fused with a 5- or 6-membered monocyclic hydrocarbon ring; and three such monocyclic heterocyclic rings A fused heterocyclic group; a heterocyclic group fused with two such monocyclic heterocycles and one 5- or 6-membered monocyclic hydrocarbon ring; or such monocyclic heterocycle 1 And a heterocyclic group formed by condensing two and five or six-membered monocyclic hydrocarbon rings. Specific examples of the 5- to 14-membered heterocyclic group include piperidinyl group, piperazinyl group, morpholinyl group, thiophenyl group, furanyl group, pyrrolyl group, imidazolyl group, pyrazolyl group, isothiazolyl group, isoxazolyl group, oxazolyl group, isoxazolyl group Group, thiazolyl group, isothiazolyl group, furazanyl group, pyranyl group, pyridyl group, pyridazinyl group, pyrimidinyl group, pyrazinyl group, indolyl group, 1H-indazolyl group, isoindolyl group, chromenyl group, quinolinyl group, isoquinolinyl group, purinyl group, pteridinyl Group, triazolyl group, tetrazolyl group, 4H-quinolidinyl group, naphthyridinyl group, benzofuranyl group, 1,3-benzodioxolyl group, benzoxazolyl group, benzothiazolyl group, benzimidazolyl group, Rubazoriru group, phenanthridinyl group, acridinyl group, phenazinyl group or include phenanthrolinyl group. Examples of the 5-membered or 6-membered heterocyclic group are 5-membered or 6-membered groups among the groups described as examples of the 5-membered to 14-membered heterocyclic group.

  A cycloalkyl group having 3 to 10 carbon atoms is unsubstituted. Examples of the cycloalkyl group having 3 to 10 carbon atoms include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, a cyclononyl group, and a cyclodecyl group.

  An aralkyl group having 7 to 20 carbon atoms is unsubstituted. The aralkyl group having 7 to 20 carbon atoms is an alkyl group having 1 to 6 carbon atoms having an aryl group having 6 to 14 carbon atoms.

<1. Electrophotographic photoreceptor>
The present embodiment relates to an electrophotographic photoreceptor (hereinafter referred to as a photoreceptor). According to the photoconductor of this embodiment, it is possible to improve the filming resistance and to suppress the generation of a transfer memory. The reason is presumed as follows.

  To help understanding, filming will be explained. Filming is a phenomenon in which minute components adhere to and adhere to the surface of the photoreceptor. An example of the minute component is a toner component, and more specifically, a toner or a free external additive. Another example of the minute component is a non-toner component, and more specifically, a minute component (for example, paper dust) of a recording medium (for example, paper). In image formation, toner or free external additives may adhere to the surface of the photoreceptor. In addition, when the recording medium comes into contact with the surface of the photoconductor in image formation, a minute component of the recording medium may adhere to the surface of the photoconductor. In particular, filming is likely to occur when a minute component of a recording medium is rubbed by a photosensitive member and the minute component is charged to a negative polarity or a positive polarity lower than a desired value.

  Here, in the photoreceptor of this embodiment, the electron transport agent includes a compound represented by the general formula (1) (hereinafter sometimes referred to as compound (1)). The compound (1) essentially has a halogen atom and has a predetermined skeleton. When such a compound (1) is contained, when the minute component of the recording medium comes into contact with the photoreceptor and the minute component is rubbed by the photosensitive member, the minute component has a negative polarity or a positive electrode lower than a desired value. It is thought that it can suppress that it is electrically charged. The surface of the photosensitive member charged to the positive polarity in the charging step of image formation and the minute component of the recording medium having a positive polarity of a desired value or more are electrically repelled. This makes it difficult for minute components to adhere to the surface of the photoreceptor. As a result, the occurrence of filming can be suppressed.

  Furthermore, in the photoreceptor of this embodiment, the photosensitive layer includes silica particles or resin particles that are filler particles. Thereby, there exists a tendency for moderate uneven | corrugated shape to be formed in the surface of a photosensitive layer. This tends to reduce the contact area between the surface of the photosensitive layer and the minute components attached to the surface of the photoreceptor. When the contact area is small, the cleaning unit easily removes minute components adhering to the surface of the photoreceptor from the surface of the photosensitive layer. As a result, the filming resistance of the photoreceptor can be improved.

  Next, in order to help understanding, the transfer memory will be described. The transfer memory is a phenomenon in which the charged potential of the area corresponding to the non-exposed area of the previous circumference is lower than the area corresponding to the exposed area of the previous circumference on the surface of the photoreceptor due to the influence of the transfer bias. A transfer memory is likely to occur when an image is formed at a high speed. This is because when an image is formed at a high speed, the transfer conditions for applying a strong transfer bias to the photoconductor are often set. Further, when an image is formed at a high speed, the charging time and the time for moving the charges in the photosensitive layer become insufficient, and charges (especially electrons) are easily accumulated in the photosensitive layer. When a transfer memory is generated on the photoconductor, an image ghost (particularly a negative ghost) is generated on the formed image. The negative ghost is an image defect in which a region corresponding to the non-exposed region on the periphery in front of the photosensitive member is blackened in the formed image.

  Here, the photosensitive layer of the photoreceptor of this embodiment includes the compound (1) that is an electron transport agent and silica particles or resin particles that are filler particles. Thereby, accumulation of electrons in the photosensitive layer can be suppressed. As a result, generation of transfer memory can be suppressed.

  Hereinafter, the structure of the photoconductor 30 will be described with reference to FIGS. FIG. 1 is a cross-sectional view showing an example of the photoreceptor 30 according to the present embodiment.

  As shown in FIG. 1A, the photoreceptor 30 includes, for example, a conductive substrate 31 and a photosensitive layer 32. The photosensitive layer 32 is a single layer. The photoconductor 30 is a so-called single layer type photoconductor provided with a single photoconductive layer 32.

  As shown in FIG. 1B, the photoreceptor 30 may include a conductive substrate 31, a photosensitive layer 32, and an undercoat layer 33 (intermediate layer). The undercoat layer 33 is provided between the conductive substrate 31 and the photosensitive layer 32. As shown in FIG. 1A, the photosensitive layer 32 may be disposed directly on the conductive substrate 31. When the surface 31 a of the conductive substrate 31 has an oxide film, the photosensitive layer 32 may be indirectly disposed on the conductive substrate 31 via the oxide film. Alternatively, as shown in FIG. 1B, the photosensitive layer 32 may be indirectly disposed on the conductive substrate 31 via the undercoat layer 33.

  As shown in FIG. 1C, the photoreceptor 30 may include a conductive substrate 31, a photosensitive layer 32, and a protective layer 34. The protective layer 34 is provided on the photosensitive layer 32. However, in order to further suppress the generation of the transfer memory and the filming, it is preferable that the photoconductor 30 does not include the protective layer 34. When the photoconductor 30 does not include the protective layer 34, the photoconductive layer 32 is provided as the outermost surface layer of the photoconductor 30.

  The thickness of the photosensitive layer 32 is not particularly limited as long as the function as the photosensitive layer can be sufficiently expressed. The thickness of the photosensitive layer 32 is preferably 5 μm or more and 100 μm or less, and more preferably 10 μm or more and 50 μm or less.

  The photosensitive layer 32 contains a charge generating agent, a hole transport agent, an electron transport agent, a binder resin, and filler particles. The photosensitive layer 32 may contain various additives as necessary. The charge generating agent, hole transporting agent, electron transporting agent, binder resin, filler particles, and components added as necessary (for example, additives) are contained in one layer (same layer). The

  The structure of the photoreceptor 30 has been described above with reference to FIGS. 1 (a) to 1 (c). Next, the elements of the photoreceptor will be described.

<1-1. Conductive substrate>
As an example of the conductive substrate, a conductive substrate formed of a conductive material can be given. Another example of the conductive substrate includes a conductive substrate including a coating layer made of a material having conductivity. Examples of the conductive material include aluminum, iron, copper, tin, platinum, silver, vanadium, molybdenum, chromium, cadmium, titanium, nickel, palladium, indium, stainless steel, and brass. These conductive materials may be used alone or in combination of two or more (for example, as an alloy). Among these materials having conductivity, aluminum or an aluminum alloy is preferable because charge transfer from the photosensitive layer to the conductive substrate is good. Further, the conductive substrate may have an oxide film of the conductive material on the surface thereof.

  The shape of the conductive substrate is appropriately selected according to the structure of the image forming apparatus. Examples of the shape of the conductive substrate include a sheet shape or a drum shape. The thickness of the conductive substrate is appropriately selected according to the shape of the conductive substrate.

<1-2. Photosensitive layer>
The photosensitive layer contains an electron transport agent, filler particles, a binder resin, a hole transport agent, and a charge generator.

(Electron transfer agent)
The photosensitive layer contains at least one compound (1) as an electron transport agent. Compound (1) is represented by general formula (1). Compound (1) is a malononitrile derivative. The photosensitive layer can contain, for example, one or two of compound (1).

In general formula (1), R ₁ is an alkyl group having 1 to 8 carbon atoms having one or more halogen atoms; a cycloalkyl group having 3 to 10 carbon atoms having one or more halogen atoms; An aryl group having 6 to 14 carbon atoms which may have an alkyl group having 1 to 6 carbon atoms; a 5- to 14-membered heterocyclic ring having one or more halogen atoms Group: or an aralkyl group having 7 or more and 20 or less carbon atoms having at least one halogen atom.

The alkyl group having 1 to 8 carbon atoms represented by R ₁ in the general formula (1) is preferably an alkyl group having 1 to 6 carbon atoms, more preferably an alkyl group having 3 to 5 carbon atoms. An n-propyl group, an n-butyl group, or a neopentyl group is particularly preferable. The alkyl group having 1 to 8 carbon atoms represented by R ₁ has one or more halogen atoms. The halogen atom contained in the alkyl group having 1 to 8 carbon atoms represented by R ₁ is preferably a chloro group or a fluoro group, and more preferably a chloro group. The number of halogen atoms contained in the alkyl group having 1 to 8 carbon atoms represented by R ₁ is preferably 1 or 2.

The cycloalkyl group having 3 to 10 carbon atoms represented by R ₁ has one or more halogen atoms. The halogen atom contained in the cycloalkyl group having 3 to 10 carbon atoms represented by R ₁ is preferably a chloro group or a fluoro group. The number of halogen atoms contained in the cycloalkyl group having 3 to 10 carbon atoms represented by R ₁ is preferably 1 or 2.

The aryl group having 6 to 14 carbon atoms represented by R ₁ is preferably a phenyl group. The aryl group having 6 to 14 carbon atoms represented by R ₁ has one or more halogen atoms. The halogen atom contained in the aryl group having 6 to 14 carbon atoms represented by R ₁ is preferably a chloro group or a fluoro group, and more preferably a chloro group. The number of halogen atoms contained in the aryl group having 6 to 14 carbon atoms represented by R ₁ is preferably 1 or 2, and more preferably 1. The aryl group having 6 to 14 carbon atoms may further have an alkyl group having 1 to 6 carbon atoms in addition to the halogen atom. The alkyl group having 1 to 6 carbon atoms, which the aryl group having 6 to 14 carbon atoms has, is preferably an alkyl group having 1 to 3 carbon atoms, and more preferably a methyl group.

The 5- to 14-membered heterocyclic group represented by R ₁ is a 5- or 6-membered monocyclic heterocycle containing 1 to 3 heteroatoms (preferably nitrogen atoms) in addition to the carbon atom. A cyclic group is preferred, and a pyridyl group is more preferred. The 5- to 14-membered heterocyclic group represented by R ₁ has one or more halogen atoms. The halogen atom contained in the 5-membered to 14-membered heterocyclic group represented by R ₁ is preferably a chloro group or a fluoro group, and more preferably a chloro group. The number of halogen atoms contained in the 5- to 14-membered heterocyclic group represented by R ₁ is preferably one or two, and more preferably one.

The aralkyl group having 7 to 20 carbon atoms represented by R ₁ is preferably an alkyl group having 1 to 6 carbon atoms to which a phenyl group is bonded, and more preferably a phenylmethyl group (benzyl group) or a phenylethyl group. preferable. The aralkyl group having 7 to 20 carbon atoms represented by R ₁ has one or more halogen atoms. The halogen atom contained in the aralkyl group having 7 to 20 carbon atoms represented by R ₁ is preferably a chloro group or a fluoro group. The number of halogen atoms contained in the aralkyl group having 7 to 20 carbon atoms represented by R ₁ is preferably one or two.

In the general formula (1), the bonding position (substitution position) of the group represented by the general formula “—COOR ₁ ” is not particularly limited. The group represented by the general formula “—COOR ₁ ” may be bonded to any of the 1-position, 2-position, 3-position and 4-position in the following chemical formula. The group represented by the general formula “—COOR ₁ ” is preferably bonded to the 1-position, 2-position or 4-position in the following chemical formula.

From the viewpoint of suppressing the generation of transfer memory and improving the filming resistance of the photoreceptor, R ₁ is an alkyl group having 1 to 8 carbon atoms having one or two halogen atoms; one halogen atom or An aryl group having 6 to 14 carbon atoms which may have an alkyl group having 1 to 6 carbon atoms; a 5- to 14-membered heterocyclic ring having 1 or 2 halogen atoms Or an aralkyl group having 7 or more and 20 or less carbon atoms having one or two halogen atoms.

  Preferable examples of compound (1) include compounds represented by chemical formulas (1-1) to (1-9). Each of the compounds represented by chemical formulas (1-1) to (1-9) may be referred to as compounds (1-1) to (1-9).

  In order to further suppress the generation of the transfer memory, among the compounds (1-1) to (1-9), the compounds (1-1), (1-2), (1-3), (1-7) ) Or (1-9) is preferably contained in the photosensitive layer. In order to further improve the filming resistance, among the compounds (1-1) to (1-9), the compounds (1-1), (1-3) (1-4) (1-5) ( 1-6) (1-7) (1-8) or (1-9) is preferably contained in the photosensitive layer. Of the compounds (1-1) to (1-9), the compounds (1-1), (1-3), ( It is preferable that 1-7) or (1-9) is contained in the photosensitive layer.

  From the viewpoint of suppressing the occurrence of transfer memory and improving the filming resistance of the photoreceptor, the compound (1) is a compound represented by the general formula (1a) (hereinafter sometimes referred to as the compound (1a)). It is preferable that

In general formula (1a), R ₂ represents an alkyl group having 1 to 8 carbon atoms having 1 or 2 halogen atoms; a 5- to 14-membered heterocyclic group having 1 halogen atom; or fluorine It represents an aralkyl group having 7 to 20 carbon atoms having one atom. Suitable examples of compound (1a) are compound (1-1), (1-3), (1-7) or (1-9).

  The content of the compound (1) is preferably 10 parts by mass or more and 200 parts by mass or less, more preferably 10 parts by mass or more and 100 parts by mass or less with respect to 100 parts by mass of the binder resin contained in the photosensitive layer. Preferably, it is 10 parts by mass or more and 75 parts by mass or less.

  The photosensitive layer may further contain an electron transport agent other than the compound (1) in addition to the compound (1). Examples of the electron transporting agent other than the compound (1) include quinone compounds, diimide compounds, hydrazone compounds, malononitrile compounds, thiopyran compounds, trinitrothioxanthone compounds, 3,4,5,7-tetranitro- 9-fluorenone compounds, dinitroanthracene compounds, dinitroacridine compounds, tetracyanoethylene, 2,4,8-trinitrothioxanthone, dinitrobenzene, dinitroacridine, succinic anhydride, maleic anhydride or dibromomaleic anhydride It is done. Examples of quinone compounds include diphenoquinone compounds, azoquinone compounds, anthraquinone compounds, naphthoquinone compounds, nitroanthraquinone compounds, and dinitroanthraquinone compounds. These electron transport agents may be used alone or in combination of two or more.

  The content of the compound (1) is preferably 80% by mass or more, more preferably 90% by mass or more, and 100% by mass with respect to the mass of the electron transport agent contained in the photosensitive layer. It is particularly preferred.

[Production Method of Compound (1)]
Compound (1) is produced, for example, according to reactions (R-1) and (R-2) or by a method analogous thereto. In addition to these reactions, appropriate steps may be included as necessary. The compounds represented by the chemical formula (A), the general formula (B), the general formula (C), and the chemical formula (D) are described as the compounds (A), (B), (C), and (D), respectively. There is. R ₁ in the formula (B) and (C) has the same meaning as R ₁ in the general formula (1).

  In the reaction (R-1), 1 molar equivalent of the compound (A) and 1 molar equivalent of the compound (B) are reacted to obtain 1 molar equivalent of the compound (C). It is preferable to add 1 mol or more and 5 mol or less of compound (B) with respect to 1 mol of compound (A). The reaction temperature for reaction (R-1) is preferably 80 ° C. or higher and 150 ° C. or lower. The reaction time for reaction (R-1) is preferably 2 hours or longer and 10 hours or shorter.

  Reaction (R-1) may be carried out in the presence of a catalyst. Examples of the catalyst include an acid catalyst, and more specifically, p-toluenesulfonic acid, camphorsulfonic acid, or pyridinium-p-toluenesulfonic acid. These catalysts may be used individually by 1 type, and may be used in combination of 2 or more type. The addition amount of the catalyst is a small amount with respect to 1 mol of the compound (A), and specifically, it is preferably 0.01 mol or more and 0.5 mol or less.

  Reaction (R-1) may be carried out in a solvent. Examples of the solvent include ethers (specifically, tetrahydrofuran, diethyl ether or dioxane), halogenated hydrocarbons (specifically, methylene chloride, chloroform or dichloroethane) or aromatic hydrocarbons (specifically, Benzene or toluene).

  In the reaction (R-2), 1 molar equivalent of the compound (C) and 1 molar equivalent of the compound (D, malononitrile) are reacted to obtain 1 molar equivalent of the compound (1). It is preferable to add 1 mol or more and 5 mol or less of compound (D) with respect to 1 mol of compound (C). The reaction temperature for reaction (R-2) is preferably 40 ° C. or higher and 120 ° C. or lower. The reaction time for reaction (R-2) is preferably from 1 hour to 10 hours.

  Reaction (R-2) may be carried out in the presence of a catalyst. Examples of the catalyst include a base catalyst, and more specifically, piperidine and piperazine.

  Reaction (R-2) may be performed in a solvent. Examples of the solvent include polar solvents, and more specifically, methanol, ethanol, n-propanol, acetone, or dioxane.

  By purifying the reaction product obtained in the reaction (R-2) as necessary, the target compound (1) can be isolated. As a purification method, a known method is appropriately employed. Purification may be performed, for example, by crystallization or silica gel chromatography. An example of the solvent used for purification is chloroform.

(Filler particles)
The photosensitive layer contains at least one of silica particles and resin particles as filler particles. The photosensitive layer can contain, for example, one or two of silica particles and resin particles. When the photosensitive layer contains two or more types of silica particles and resin particles, the filler particles may be two or more types of silica particles, two or more types of resin particles, or one or more types of filler particles. Silica particles and one or more resin particles may be used.

  Examples of the resin particles are silicone resin particles, polyphenylene sulfide resin (hereinafter sometimes referred to as PPS resin) particles, or polytetrafluoroethylene resin (hereinafter sometimes referred to as PTFE resin) particles. From the viewpoint of improving the filming resistance of the photoreceptor, the filler particles are preferably resin particles, more preferably silicone resin particles or PTFE resin particles, and particularly preferably PTFE resin particles. From the viewpoint of improving the filming resistance of the photoreceptor, the resin particles preferably contain a halogen atom, more preferably a fluorine atom. An example of resin particles containing fluorine atoms is PTFE resin particles. The filler particles preferably do not have conductivity. Since the filler particles do not have conductivity, the surface of the photosensitive layer is easily charged uniformly.

The volume median diameter D ₅₀ of the filler particles is preferably 5 nm (ie 0.005 μm) or more and 10 μm or less from the viewpoint of further suppressing the generation of transfer memory while improving the filming resistance of the photoreceptor. It is preferably 500 μm or more and 5.000 μm or less, and more preferably 0.500 μm or more and 3.000 μm or less.

The volume median diameter D ₅₀ of the filler particles is preferably 5 nm (that is, 0.005 μm) or more and 10 μm or less from the viewpoint of further improving the filming resistance of the photoreceptor while suppressing the occurrence of transfer memory. More preferably, the thickness is from 010 μm to 10.000 μm, still more preferably from 0.400 μm to 10.000 μm, still more preferably from 1.000 μm to 10.000 μm, and from 1.000 μm to 5.000 μm. It is particularly preferably 000 μm or less, and most preferably 1.000 μm or more and 3.000 μm or less.

The volume median diameter D ₅₀ of the filler particles is measured using a precision particle size distribution measuring apparatus (“Coulter Counter Multitizer 3” manufactured by Beckman Coulter, Inc.). The volume median diameter D ₅₀ means the median diameter calculated by volume using a Coulter counter method.

  The content of the filler particles is 0.5 parts by mass or more with respect to 100 parts by mass of the binder resin contained in the photosensitive layer from the viewpoint of further improving the filming resistance of the photoreceptor and further suppressing the generation of the transfer memory. It is preferably 30 parts by mass or less, more preferably 0.5 parts by mass or more and 20 parts by mass or less, and further preferably 3 parts by mass or more and 10 parts by mass or less.

  A commercial item can also be used as a filler particle. Examples of commercially available filler particles are filler particles (F1) to (F10) shown in Table 1. Table 1 shows the type, material, volume median diameter, trade name, and manufacturer of the filler particles. The resin of filler particles (F7) to (F10) contains a fluorine atom. “AEROSIL”, “Trepearl” and “Lublon” are registered trademarks.

  When the photosensitive layer contains two types of silica particles and resin particles, the photosensitive layer preferably contains one type of silica particles and one type of resin particle, more preferably contains silica particles and PTFE resin, It is particularly preferred that the particles (F1) and (F7) are included.

  The photosensitive layer may further include filler particles (other filler particles) other than the resin particles and silica particles in addition to at least one of resin particles and silica particles. The content of at least one of the resin particles and silica particles is preferably 80% by mass or more, more preferably 90% by mass or more, with respect to the mass of the filler particles contained in the photosensitive layer. It is particularly preferable that the content is mass%.

(Binder resin)
Examples of the binder resin include a thermoplastic resin, a thermosetting resin, and a photocurable resin. Examples of the thermoplastic resin include polycarbonate resin, polyarylate resin, styrene-butadiene resin, styrene-acrylonitrile resin, styrene-maleic acid resin, acrylic acid resin, styrene-acrylic acid resin, polyethylene resin, and ethylene-vinyl acetate resin. , Chlorinated polyethylene resin, polyvinyl chloride resin, polypropylene resin, ionomer resin, vinyl chloride-vinyl acetate resin, alkyd resin, polyamide resin, urethane resin, polysulfone resin, diallyl phthalate resin, ketone resin, polyvinyl butyral resin, polyester resin or A polyether resin is mentioned. As a thermosetting resin, a silicone resin, an epoxy resin, a phenol resin, a urea resin, or a melamine resin is mentioned, for example. Examples of the photocurable resin include an epoxy-acrylic acid resin (more specifically, an acrylic acid derivative adduct of an epoxy compound) or a urethane-acrylic resin (acrylic acid derivative adduct of a urethane compound). Can be mentioned. These binder resins may be used individually by 1 type, and may be used in combination of 2 or more type.

  Among these resins, a polycarbonate resin or a polyarylate resin is preferable because a photosensitive layer having an excellent balance of workability, mechanical properties, optical properties, and abrasion resistance can be obtained. Furthermore, from the viewpoint of good compatibility with the compound (1) and improving the dispersibility of the compound (1) in the photosensitive layer, the photosensitive layer is composed of a repeating unit represented by the general formula (2) and a general unit. It is more preferable to contain at least one resin having at least one repeating unit represented by formula (3). The photosensitive layer can contain 1 type or 2 types of resin which has at least 1 sort (s) of the repeating unit represented by General formula (2) and General formula (3), for example. Moreover, the photosensitive layer can contain 1 type or 2 types of resin which has 1 type of the repeating unit represented, for example by the repeating unit represented by General formula (2), and General formula (3).

In General Formula (2), R ¹¹ and R ¹² represent a hydrogen group, an alkyl group having 1 to 6 carbon atoms which may have a halogen atom, or a phenyl group which may have a substituent. R ¹¹ and R ¹² may be bonded to each other to represent a cycloalkylidene group. R ¹¹ and R ¹² may be the same or different from each other. R ¹³ and R ¹⁴ represent an alkyl group having 1 to 3 carbon atoms which may have a hydrogen atom or a halogen atom. R ¹³ and R ¹⁴ may be the same or different from each other.

In general formula (3), it represents a hydrogen atom, an alkyl group having 1 to 6 carbon atoms which may have a halogen atom, or a phenyl group which may have a substituent. R ¹⁵ and R ¹⁶ may be bonded to each other to represent a cycloalkylidene group. R ¹⁵ and R ¹⁶ may be the same as or different from each other. R ¹⁷ and R ¹⁸ represent an alkyl group having 1 to 3 carbon atoms which may have a hydrogen atom or a halogen atom. R ¹⁷ and R ¹⁸ may be the same or different from each other. Regarding the substitution position of two carbonyl groups in the general formula (3), one carbonyl group is in the ortho position (o position), meta (m position) or para position with respect to the other carbonyl group bonded to the benzene ring. Located at (p position).

  When the binder resin has two or more of the repeating unit represented by the general formula (2) and the repeating unit represented by the general formula (3), the binder resin is represented by two or more general formulas (2). May have a repeating unit represented, may have two or more repeating units represented by general formula (3), and may be represented by one or more general formulas (2) You may have a unit and the repeating unit represented by 1 or more types of General formula (3).

  The resin having two or more types of repeating units represented by the general formula (2) is, for example, a copolymer of two or more types of alcohol monomers and phosgene for forming the repeating units represented by the general formula (2). By making it, it can manufacture. Resins having two or more types of repeating units represented by the general formula (3) are, for example, two or more types of alcohol monomers and two or more types of carboxyls for forming the repeating units represented by the general formula (3). It can be produced by copolymerizing with an acid monomer. The resin having one or more types of repeating units represented by the general formula (2) and one or more types of repeating units represented by the general formula (3) is, for example, a repeating unit represented by the general formula (2). Copolymerizing one or more alcohol monomers and phosgene for forming with one or more alcohol monomers and one or more carboxylic acid monomers for forming a repeating unit represented by the general formula (3); Can be manufactured.

  Examples of the resin having at least one of the repeating unit represented by the general formula (2) and the repeating unit represented by the general formula (3) include a polycarbonate resin having a repeating unit represented by the general formula (2) or It is a polyarylate resin having a repeating unit represented by the general formula (3). Hereinafter, the polycarbonate resin having a repeating unit represented by the general formula (2) may be referred to as a polycarbonate resin (2). Moreover, the polyarylate resin which has a repeating unit represented by General formula (3) may be described as a polyarylate resin (3).

  The photosensitive layer preferably contains at least one of a polycarbonate resin (2) and a polyarylate resin (3). The photosensitive layer can contain, for example, one or two of a polycarbonate resin (2) and a polyarylate resin (3). When the photosensitive layer contains two or more kinds of polycarbonate resin (2) and polyarylate resin (3), the binder resin may be two or more kinds of polycarbonate resins (2), and two or more kinds of polyarylate. Resin (3) may be sufficient and 1 or more types of polycarbonate resins (2) and 1 or more types of polyarylate resin (3) may be sufficient.

  Hereinafter, the polycarbonate resin (2) will be described.

In general formula (2), the alkyl group having 1 to 6 carbon atoms which may have a halogen atom represented by R ¹¹ and R ¹² is preferably an alkyl group having 1 to 4 carbon atoms, and a methyl group is More preferred.

When R ¹¹ and R ¹² in the general formula (2) are bonded to each other to form a cycloalkylidene group, such a cycloalkylidene group is preferably a cycloalkylidene group having 5 to 7 carbon atoms. A den group is more preferred. When R ¹¹ and R ¹² in the general formula (2) are bonded to each other to represent a cycloalkylidene group having 5 to 7 carbon atoms, the general formula (2) corresponds to the general formula (2 ′). R ¹³ and R ¹⁴ in the general formula (2 ') has the general formula (2) have the same meanings as R ¹³ and ¹⁴ of the ring A represents a cycloalkane 5 to 7 carbon atoms.

In general formula (2), R ¹¹ and R ¹² represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, or R ¹¹ and R ¹² are bonded to each other to form a cycloalkylidene having 5 to 7 carbon atoms. It is preferable to represent a group. More preferably, R ¹¹ and R ¹² represent a hydrogen atom or a methyl group, or R ¹¹ and R ¹² are bonded to each other to represent a cyclohexylidene group.

In general formula (2), the alkyl group having 1 to 3 carbon atoms which may have a halogen atom represented by R ¹³ and R ¹⁴ is preferably a methyl group which may have a halogen atom. Or a methyl fluoride group is more preferable, and a methyl group or a trifluoromethyl group is still more preferable.

In general formula (2), R ¹³ and R ¹⁴ preferably represent a hydrogen atom or a methyl group which may have a halogen atom, more preferably a hydrogen atom, a methyl group or a methyl fluoride group, More preferably, it represents a hydrogen atom, a methyl group or a trifluoromethyl group. R ¹³ and R ¹⁴ are preferably the same as each other. In general formula (2), it is preferable that at least one of R ¹¹ , R ¹² , R ¹³ and R ¹⁴ has one or more halogen atoms.

  A suitable example of the polycarbonate resin (2) is a polycarbonate having a repeating unit represented by the chemical formula (PC-1), (PC-2), (PC-3), (PC-4) or (PC-5). Resin (hereinafter, may be referred to as polycarbonate resins (PC-1) to (PC-5), respectively).

  The polycarbonate resin (2) may have one type of repeating unit represented by the general formula (2), or may have two or more types of repeating units represented by the general formula (2). Good.

  The ratio (molar fraction) of the number of moles of the repeating unit represented by the general formula (2) to the number of moles of all the repeating units of the polycarbonate resin (2) is preferably 80% by mole or more, and 90% by mole. More preferably, it is 100 mol%.

  The content of the polycarbonate resin (2) with respect to the mass of the binder resin contained in the photosensitive layer is preferably 80% by mass or more, more preferably 90% by mass or more, and particularly preferably 100% by mass. .

  Hereinafter, the polyarylate resin (3) will be described.

In general formula (3), the alkyl group having 1 to 6 carbon atoms which may have a halogen atom represented by R ¹⁵ and R ¹⁶ is preferably an alkyl group having 1 to 6 carbon atoms, An alkyl group having 1 or more and 3 or less is more preferable, and a methyl group is more preferable.

In general formula (3), the phenyl group represented by R ¹⁵ and R ¹⁶ may have a substituent. Examples of such a substituent include a halogen atom, a hydroxyl group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, and a cyano group.

In the case where R ¹⁵ and R ¹⁶ in the general formula (3) are bonded to each other to form a cycloalkylidene group, such a cycloalkylidene group is preferably a cycloalkylidene group having 5 to 7 carbon atoms. A den group is more preferred. When R ¹⁵ and R ¹⁶ in the general formula (3) are bonded to each other to represent a cycloalkylidene group having 5 to 7 carbon atoms, the general formula (3) corresponds to the general formula (3 ′). R ¹⁷ and R ¹⁸ in the general formula (3 ') has the general formula (3) have the same meanings as R ¹⁷ and ¹⁸ of ring B represents a cycloalkane 5 to 7 carbon atoms.

In general formula (3), the alkyl group having 1 to 3 carbon atoms which may have a halogen atom represented by R ¹⁷ and R ¹⁸ is preferably an alkyl group having 1 to 3 carbon atoms, and a methyl group Is more preferable.

In General Formula (3), R ¹⁵ and R ¹⁶ preferably represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, and more preferably represent a hydrogen atom or a methyl group. R ¹⁵ and R ¹⁶ are preferably different from each other. R ¹⁷ and R ¹⁸ preferably represent an alkyl group having 1 to 3 carbon atoms, and more preferably represent a methyl group. R ¹⁷ and R ¹⁸ are preferably the same as each other. R ¹⁹ and R ²⁰ preferably represent a hydrogen atom. From the viewpoint of further improving the filming resistance of the photoreceptor, it is preferable that at least one of R ¹⁵ , R ¹⁶ , R ¹⁷ and R ^{18 in} the general formula (3) has one or more halogen atoms.

  A suitable example of the polyarylate resin (3) is a polyarylate resin having a repeating unit represented by the chemical formula (PAR-1) (hereinafter sometimes referred to as polyarylate resin (PAR-1)).

  The polyarylate resin (3) may have one type of repeating unit represented by the general formula (3), and may have two or more types of repeating units represented by the general formula (3). Also good.

  The ratio (molar fraction) of the number of moles of the repeating unit represented by the general formula (3) to the number of moles of all the repeating units of the polyarylate resin (3) is preferably 80 mole% or more, and 90 moles. % Or more is more preferable, and 100 mol% is particularly preferable.

  The content of the polyarylate resin (3) with respect to the mass of the binder resin contained in the photosensitive layer is preferably 80% by mass or more, more preferably 90% by mass or more, and particularly preferably 100% by mass. preferable.

  In order to further suppress the generation of transfer memory, polycarbonate resins (PC-1), (PC-2), (PC-3), (PC-4) and (PC-5) and polyarylate resins (PAR-) are used. Among 1), the binder resin is preferably polycarbonate resin (PC-1) or (PC-3).

  In order to further improve the filming resistance, polycarbonate resins (PC-1), (PC-2), (PC-3), (PC-4) and (PC-5) and polyarylate resins (PAR-) are used. Of 1), the binder resin is preferably polycarbonate resin (PC-1), (PC-2), (PC-3) or (PC-4).

  In order to further reduce the occurrence of transfer memory and improve the filming resistance, polycarbonate resins (PC-1), (PC-2), (PC-3), (PC-4) and (PC-) 5) Of the polyarylate resin (PAR-1), the binder resin is preferably a polycarbonate resin (PC-1) or (PC-3).

  From the viewpoint of further improving the filming property of the photoreceptor and suppressing the generation of the transfer memory, the preferred combinations of the filler particles, the electron transport agent and the binder resin are as follows. The filler particles are resin particles containing fluorine atoms (preferably PTFE). The electron transfer agent is the compound (1-1), (1-3), (1-7) or (1-9). The binder resin is a polycarbonate resin (PC-1) or (PC-3). In this combination, the content of the filler particles is preferably 3 parts by mass or more and 10 parts by mass or less with respect to 100 parts by mass of the binder resin.

  The viscosity average molecular weight of the binder resin is preferably 20000 or more, more preferably 30000 or more and 70000 or less, and further preferably 48500 or more and 50000 or less. When the viscosity average molecular weight of the binder resin is 20000 or more, it is easy to improve the abrasion resistance of the photoreceptor. When the viscosity average molecular weight of the binder resin is 70000 or less, the binder resin is easily dissolved in the solvent for forming the photosensitive layer, and the viscosity of the coating solution for the photosensitive layer does not become too high. As a result, it becomes easy to form a photosensitive layer.

(Hole transport agent)
As the hole transport agent, for example, a nitrogen-containing cyclic compound or a condensed polycyclic compound can be used. Examples of the nitrogen-containing cyclic compound and the condensed polycyclic compound include diamine derivatives (more specifically, N, N, N ′, N′-tetraphenylphenylenediamine derivatives, N, N, N ′, N ′). -Tetraphenylnaphthylenediamine derivative or N, N, N ', N'-tetraphenylphenanthrylenediamine derivative, etc.), oxadiazole compounds (more specifically, 2,5-di (4-methylamino) Phenyl) -1,3,4-oxadiazole, etc.), styryl compounds (more specifically, 9- (4-diethylaminostyryl) anthracene, etc.), carbazole compounds (more specifically, polyvinylcarbazole, etc.), Organic polysilane compounds, pyrazoline compounds (more specifically, 1-phenyl-3- (p-dimethylaminophenyl) pyrazoline etc.), hydrazones Compounds, indole compounds, oxazole compounds, isoxazole compounds, thiazole compounds, thiadiazole compounds, imidazole compounds, pyrazole compound, or triazole-based compounds. These hole transport agents may be used alone or in combination of two or more.

  Suitable examples of the hole transporting agent include general formula (HTM1), general formula (HTM2), general formula (HTM3), general formula (HTM4), general formula (HTM5), general formula (HTM6), or general formula (HTM7). ) (Hereinafter may be referred to as compounds (HTM1) to (HTM7)).

  Hereinafter, the compound (HTM1) will be described.

In the general formula (HTM1), Q ⁸ , Q ¹⁰ , Q ¹¹ , Q ¹² , Q ¹³ and Q ¹⁴ are each independently a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, or 1 to 6 carbon atoms. The following alkoxy groups or phenyl groups are represented. Q ⁹ and Q ¹⁵ each independently represents an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or a phenyl group. b represents an integer of 0 or more and 5 or less. c represents an integer of 0 or more and 4 or less. k represents 0 or 1.

When b represents an integer of 2 or more and 5 or less, a plurality of Q ⁹ bonded to the same phenyl group may be the same as or different from each other. When c represents an integer of 2 or more and 4 or less, the plurality of Q ¹⁵ bonded to the same phenylene group may be the same as or different from each other.

In the general formula (HTM1), Q ⁸ , Q ¹⁰ , Q ¹¹ , Q ¹² , Q ¹³ and Q ¹⁴ preferably represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, a hydrogen atom, a methyl group Or it represents more preferably an ethyl group. b and c preferably represent 0. k preferably represents 0. Examples of the compound (HTM1) include a compound represented by the chemical formula (HTM1-1) (hereinafter sometimes referred to as the compound (HTM1-1)).

  Hereinafter, the compound (HTM2) will be described.

In general formula (HTM2), Q ¹ has a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or an alkyl group having 1 to 6 carbon atoms. Represents a good phenyl group. Two Q ¹ may be the same or different. Q ² represents an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or a phenyl group. Q ³ , Q ⁴ , Q ⁵ , Q ⁶ and Q ⁷ each independently represent a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or a phenyl group. Two adjacent ones of Q ³ , Q ⁴ , Q ⁵ , Q ⁶ and Q ⁷ may be bonded to each other to represent a ring. a represents an integer of 0 or more and 5 or less. t and u each independently represents an integer of 0 or more and 2 or less.

When a represents an integer of 2 or more and 5 or less, a plurality of Q ² bonded to the same phenyl group may be the same or different from each other.

In general formula (HTM2), Q ¹ preferably represents a hydrogen atom. Q ³ , Q ⁴ , Q ⁵ , Q ⁶ and Q ⁷ each independently preferably represent a hydrogen atom, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 6 carbon atoms, More preferably, it represents a hydrogen atom, an n-butyl group or an ethoxy group. It is preferable that a represents 0. It is preferable that t and u represent 1. Examples of the compound (HTM2) include a compound represented by the chemical formula (HTM2-1) or (HTM2-2) (hereinafter sometimes referred to as the compound (HTM2-1) or (HTM2-2)). It is done.

  Hereinafter, the compound (HTM3) will be described.

In the general formula (HTM3), Q ¹⁶ , Q ¹⁷ , Q ¹⁸ and Q ¹⁹ each independently represents an alkyl group having 1 to 4 carbon atoms. Q ¹⁶ , Q ¹⁷ , Q ¹⁸ and Q ¹⁹ each independently preferably represent a methyl group or an n-butyl group. Examples of the compound (HTM3) include a compound represented by the chemical formula (HTM3-1) (hereinafter sometimes referred to as the compound (HTM3-1)).

  Hereinafter, the compound (HTM4) will be described.

In the general formula (HTM4), Q ²⁰ , Q ²¹ , Q ²² and Q ²³ each independently represents an alkyl group having 1 to 4 carbon atoms. v1, v2, v3 and v4 each independently represent an integer of 0 or more and 5 or less.

When v1 represents an integer of 2 or more and 5 or less, the plurality of Q ²⁰ may be the same as or different from each other. When v2 represents an integer of 2 or more and 5 or less, the plurality of Q ²¹ may be the same as or different from each other. When v3 represents an integer of 2 or more and 5 or less, the plurality of Q ²² may be the same as or different from each other. When v4 represents an integer of 2 or more and 5 or less, the plurality of Q ²³ may be the same as or different from each other.

In general formula (HTM4), Q ²⁰ , Q ²¹ , Q ²² and Q ²³ preferably represent a methyl group. v1 and v2 preferably represent 1. v3 and v4 preferably represent 0. Examples of the compound (HTM4) include a compound represented by the chemical formula (HTM4-1) (hereinafter sometimes referred to as the compound (HTM4-1)).

  Hereinafter, the compound (HTM5) will be described.

In the general formula (HTM5), R ^d , R ^e and R ^f each independently represents an alkyl group having 1 to 6 carbon atoms. o, p, and r each independently represent an integer of 0 or more and 5 or less.

When o represents an integer of 2 or more and 5 or less, a plurality of R ^e bonded to the same phenyl group may be the same or different. When p represents an integer of 2 or more and 5 or less, a plurality of R ^f bonded to the same phenyl group may be the same or different from each other. When r represents an integer of 2 or more and 5 or less, a plurality of R ^d bonded to the same phenyl group may be the same or different from each other.

In general formula (HTM5), R ^e preferably represents an alkyl group having 1 to 3 carbon atoms, and more preferably a methyl group or an ethyl group. o preferably represents 2. p and r preferably represent 0. Examples of the compound (HTM5) include a compound represented by the chemical formula (HTM5-1) (hereinafter sometimes referred to as the compound (HTM5-1)).

  The compound (HTM6) will be described.

In General Formula (HTM6), R ^a , R ^b, and R ^c each independently represent an alkyl group having 1 to 6 carbon atoms, a phenyl group, or an alkoxy group having 1 to 6 carbon atoms. q represents an integer of 0 or more and 4 or less. s and n each independently represent an integer of 0 or more and 5 or less.

When q represents an integer of 2 or more and 4 or less, a plurality of R ^c bonded to the same phenylene group may be the same as or different from each other. When s represents an integer of 2 or more and 5 or less, a plurality of R ^b bonded to the same phenyl group may be the same or different from each other. When n represents an integer of 2 or more and 5 or less, a plurality of R ^a bonded to the same phenyl group may be the same or different from each other.

In general formula (HTM6), R ^a and R ^b are each independently preferably an alkyl group having 1 to 3 carbon atoms, and more preferably a methyl group or an ethyl group. It is preferable that s and n each independently represent 0, 1 or 2. More preferably, one of s and n represents 0 or 1, and the other of s and n represents 2. q preferably represents 0. Examples of the compound (HTM6) include a compound represented by the chemical formula (HTM6-1) or (HTM6-2) (hereinafter sometimes referred to as the compound (HTM6-1) or (HTM6-2)). It is done.

  Hereinafter, the compound (HTM7) will be described.

In the general formula (HTM7), Q ³¹ , Q ³³ and Q ³⁵ each independently represent an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or a phenyl group. Q ³² , Q ³⁴ and Q ³⁶ are each independently a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms or an alkyl group having 1 to 6 carbon atoms. Represents an optionally substituted phenyl group. d, e, and f each independently represent 0 or 1. g, h and i each independently represents an integer of 0 or more and 5 or less.

When g represents an integer of 2 or more and 5 or less, the plurality of Q ³¹ may be the same as or different from each other. When h represents an integer of 2 or more and 5 or less, the plurality of Q ³³ may be the same or different from each other. When i represents an integer of 2 or more and 5 or less, the plurality of Q ³⁵ may be the same or different from each other.

In the general formula (HTM7), Q ³¹ , Q ³³ and Q ³⁵ preferably represent an alkyl group having 1 to 3 carbon atoms, and more preferably represent a methyl group. d, e and f preferably represent 0. Q ³² , Q ³⁴ and Q ³⁶ preferably represent a hydrogen atom. g, h and i preferably represent 1. Examples of the compound (HTM7) include a compound represented by the chemical formula (HTM7-1) (hereinafter sometimes referred to as the compound (HTM7-1)).

  In order to suppress the generation of the transfer memory, the hole transport agent is preferably any one of the compounds (HTM1) to (HTM7), and the compound (HTM1), (HTM2), (HTM4) or (HTM6) More preferably, it is more preferably compound (HTM1) or (HTM2), and particularly preferably compound (HTM1-1), (HTM2-1) or (HTM2-2).

  In order to improve the filming resistance, the hole transport agent is preferably any one of the compounds (HTM1) to (HTM7), and the compound (HTM1), (HTM2), (HTM4) or (HTM6) More preferably, the compound (HTM1), (HTM2) or (HTM4) is more preferable, and the compound (HTM1-1), (HTM2-1), (HTM2-2) or (HTM4-1) More preferably it is.

  In order to further satisfy the suppression of the generation of transfer memory and the improvement of filming resistance, the hole transport agent is preferably any one of compounds (HTM1) to (HTM7), and is preferably compound (HTM1) or (HTM2). It is more preferable that it is a compound (HTM1-1), (HTM2-1) or (HTM2-2).

  From the viewpoint of further improving the filming property of the photoreceptor and suppressing the generation of the transfer memory, the preferred combinations of the filler particles, the electron transport agent, the binder resin, and the hole transport agent are as follows. The filler particles are resin particles containing fluorine atoms (preferably PTFE). The electron transfer agent is the compound (1-1), (1-3), (1-7) or (1-9). The binder resin is a polycarbonate resin (PC-1) or (PC-3). The hole transport agent is compound (HTM1) or (HTM2) (preferably compound (HTM1-1), (HTM2-1) or (HTM2-2)). In this combination, the content of the filler particles is preferably 3 parts by mass or more and 10 parts by mass or less with respect to 100 parts by mass of the binder resin.

  The content of the hole transport agent is preferably 10 parts by mass or more and 300 parts by mass or less, and preferably 10 parts by mass or more and 200 parts by mass or less with respect to 100 parts by mass of the binder resin contained in the photosensitive layer. More preferably, it is 10 parts by mass or more and 100 parts by mass or less.

(Charge generator)
The photosensitive layer contains a charge generating agent. The charge generating agent preferably contains metal phthalocyanine or metal-free phthalocyanine. A charge generating agent may be used individually by 1 type, and may be used in combination of 2 or more type.

  Examples of the metal phthalocyanine include titanyl phthalocyanine, hydroxygallium phthalocyanine, or chlorogallium phthalocyanine represented by the chemical formula (CGM-A). Metal-free phthalocyanine is represented, for example, by the chemical formula (CGM-B). The metal phthalocyanine and the metal-free phthalocyanine may be crystalline or non-crystalline. There are no particular limitations on the crystal shapes of metal phthalocyanine and metal-free phthalocyanine (for example, α-type, β-type, Y-type, V-type or II-type), and metal phthalocyanine and metal-free phthalocyanine having various crystal shapes are used. .

  Examples of the crystal of metal-free phthalocyanine include an X-type crystal of metal-free phthalocyanine (hereinafter sometimes referred to as X-type metal-free phthalocyanine). Examples of the crystal of metal phthalocyanine include a crystal of titanyl phthalocyanine. Examples of the crystal of titanyl phthalocyanine include α-type, β-type, and Y-type crystals of titanyl phthalocyanine (hereinafter sometimes referred to as α-type, β-type, or Y-type titanyl phthalocyanine).

  For example, in a digital optical image forming apparatus (for example, a laser beam printer or a facsimile using a light source such as a semiconductor laser), it is preferable to use a photoreceptor having sensitivity in a wavelength region of 700 nm or more. Since it has a high quantum yield in a wavelength region of 700 nm or more, the charge generator is preferably a phthalocyanine pigment, more preferably a metal-free phthalocyanine or titanyl phthalocyanine, an X-type metal-free phthalocyanine, an α-type titanyl phthalocyanine or a Y-type. Titanyl phthalocyanine is more preferred, and Y-type titanyl phthalocyanine is particularly preferred. In addition, Y-type titanyl phthalocyanine has the advantages of high charge generation efficiency and less charge remaining in the photosensitive layer.

  Y-type titanyl phthalocyanine has a main peak at 27.2 ° of the Bragg angle (2θ ± 0.2 °) in the CuKα characteristic X-ray diffraction spectrum, for example. The main peak in the CuKα characteristic X-ray diffraction spectrum is a peak having the first or second highest intensity in a range where the Bragg angle (2θ ± 0.2 °) is 3 ° or more and 40 ° or less. Y-type titanyl phthalocyanine has no peak at 26.2 ° C. in the CuKα characteristic X-ray diffraction spectrum.

  An example of a method for measuring the CuKα characteristic X-ray diffraction spectrum will be described. A sample (titanyl phthalocyanine) is filled in a sample holder of an X-ray diffractometer (for example, “RINT (registered trademark) 1100” manufactured by Rigaku Corporation), an X-ray tube Cu, a tube voltage 40 kV, a tube current 30 mA, and CuKα. An X-ray diffraction spectrum is measured under the condition of a characteristic X-ray wavelength of 1.542 mm. The measurement range (2θ) is, for example, 3 ° to 40 ° (start angle 3 °, stop angle 40 °), and the scanning speed is, for example, 10 ° / min. The main peak is determined from the obtained X-ray diffraction spectrum, and the Bragg angle of the main peak is read.

  FIG. 2 is an example of a CuKα characteristic X-ray diffraction spectrum chart of titanyl phthalocyanine used in the photoreceptor according to the present embodiment. In FIG. 2, the horizontal axis indicates the Bragg angle 2θ (°), and the vertical axis indicates the intensity (cps). From the CuKα characteristic X-ray diffraction spectrum chart of FIG. 2, it can be estimated that the measured crystal form of titanyl phthalocyanine is Y-type.

(Method for preparing Y-type titanyl phthalocyanine crystal)
The method for preparing Y-type titanyl phthalocyanine crystal includes, for example, a synthesis step, a pre-pigmentation step, and a pigmentation step.

(Synthesis process)
In the synthesis step, titanyl phthalocyanine is synthesized. Examples of the method for synthesizing titanyl phthalocyanine include reaction (RA) or (RB).

  In an example reaction (R-A), phthalonitrile (21a) and titanium alkoxide (21b) are reacted to synthesize titanyl phthalocyanine (CGM-A).

  In another example reaction (RB), 1,3-diiminoisoindoline (21c) and titanium alkoxide (21b) are reacted to synthesize titanyl phthalocyanine (CGM-A).

(Pre-pigmentation process)
In the pre-pigmentation treatment step, a stirring treatment and a stationary treatment are performed to stabilize titanyl phthalocyanine (CGM-A). In the stirring treatment, titanyl phthalocyanine (CGM-A) is added to a water-soluble organic solvent to prepare a solution. The solution is stirred for a certain time while the solution is heated. The heating temperature is preferably 70 ° C. or higher and 200 ° C. or lower. The stirring time is preferably 1 hour or more and 3 hours or less. In the standing treatment, the solution is allowed to stand for stabilization for a certain period of time at a low temperature. The low temperature indicates a temperature lower than the temperature in the stirring process. The low temperature is preferably 10 ° C. or more and 50 ° C. or less, and more preferably room temperature (for example, 23 ° C.). The standing time is preferably 5 hours or more and 10 hours or less. By removing the water-soluble organic solvent, a crude crystal of titanyl phthalocyanine (CGM-A) is obtained.

  Examples of the water-soluble organic solvent include methanol, ethanol, isopropanol, N, N-dimethylformamide, N, N-dimethylacetamide, propionic acid, acetic acid, N-methylpyrrolidone, or ethylene glycol. One of these water-soluble organic solvents may be used alone, or two or more thereof may be used in combination.

(Pigmentation process)
In the pigmentation step, titanyl phthalocyanine is pigmented. An example of the pigmentation process will be described. A crude crystal of titanyl phthalocyanine (CGM-A) is dissolved in a solvent to prepare a titanyl phthalocyanine solution. This solution is dropped into a poor solvent and recrystallized. Subsequently, it is pigmented through processes such as filtration, washing with water, milling and drying. As a result, a Y-type titanyl phthalocyanine crystal is obtained.

  Examples of the solvent that dissolves the crude crystals include dichloromethane, chloroform, ethyl bromide, butyl bromide, trifluoroacetic acid, trichloroacetic acid, tribromoacetic acid, and sulfuric acid. These solvent may be used individually by 1 type, and may be used in combination of 2 or more type.

  Examples of the poor solvent for recrystallization include water, methanol, ethanol, isopropanol, acetone, and dioxane. These poor solvents may be used alone or in combination of two or more.

  The milling process is a process of dispersing and stirring in a non-aqueous solvent in a state where water is present without drying the solid after washing with water. Examples of non-aqueous solvents for milling include halogen solvents (more specifically, chlorobenzene, dichloromethane, etc.).

  Another example of the pigmentation process will be described. The crude crystal of titanyl phthalocyanine (CGM-A) is processed by the acid paste method. Specifically, an acid solution is prepared by dissolving crude crystals in an acid. The acid solution is dropped into water under ice cooling and stirred for a certain time. Subsequently, it is recrystallized by standing at room temperature (for example, 23 ° C.). As a result, low crystalline titanyl phthalocyanine is obtained. Examples of the acid used in the acid paste method include concentrated sulfuric acid or sulfonic acid.

  Low crystalline titanyl phthalocyanine is filtered and washed with water. Next, in a state where water is present without drying, a low crystalline titanyl phthalocyanine is dispersed in a non-aqueous solvent, and a milling process is performed. Filtration is performed after milling to obtain a filtrate (solid). When the filtrate is dried, Y-type titanyl phthalocyanine crystals are obtained.

  In a photoreceptor applied to an image forming apparatus using a short wavelength laser light source (for example, a laser light source having a wavelength of 350 nm or more and 550 nm or less), an sanslon pigment is preferably used as a charge generating agent.

  In addition to metal phthalocyanine or metal-free phthalocyanine, the photosensitive layer further contains another charge generator other than metal phthalocyanine and metal-free phthalocyanine (hereinafter sometimes referred to as another charge generator) as a charge generator. May be. The charge generator may further contain another charge generator in addition to the metal phthalocyanine or the metal-free phthalocyanine. Other charge generators include, for example, perylene pigments, bisazo pigments, trisazo pigments, dithioketopyrrolopyrrole pigments, metal-free naphthalocyanine pigments, metal naphthalocyanine pigments, squaraine pigments, indigo pigments, azulenium pigments, cyanine pigments, inorganic pigments Powders of photoconductive materials (more specifically, selenium, selenium-tellurium, selenium-arsenic, cadmium sulfide, amorphous silicon, etc.), pyrylium pigments, ansanthrone pigments, triphenylmethane pigments, selenium pigments, toluidine pigments, pyrazoline pigments Or a quinacridone pigment is mentioned. Another charge generating agent may be used alone or in combination of two or more.

  The content of metal phthalocyanine or metal-free phthalocyanine is preferably 80% by mass or more, preferably 90% by mass or more, and particularly preferably 100% by mass with respect to the mass of the charge generating agent.

  The content of the charge generating agent is preferably 0.1 parts by weight or more and 50 parts by weight or less, and 0.5 parts by weight or more and 30 parts by weight or less with respect to 100 parts by weight of the binder resin contained in the photosensitive layer. More preferably, it is 1 to 5 parts by mass.

<1-3. Undercoat layer>
The undercoat layer contains, for example, inorganic particles and a resin (undercoat layer resin) used for the undercoat layer. The presence of the undercoat layer is considered to suppress the increase in resistance by smoothing the flow of current generated when the photosensitive member is exposed while maintaining an insulating state capable of suppressing the occurrence of leakage.

  Examples of the inorganic particles include metal (for example, aluminum, iron or copper), metal oxide (for example, titanium oxide, alumina, zirconium oxide, tin oxide or zinc oxide) particles or non-metal oxide (for example, silica). Particles. These inorganic particles may be used individually by 1 type, and may use 2 or more types together.

  The resin for the undercoat layer is not particularly limited as long as it can be used as a resin for forming the undercoat layer. The undercoat layer may contain various additives.

<1-4. Photoconductor manufacturing method>
The photoreceptor is manufactured, for example, as follows. The photoreceptor is produced by applying a coating solution for the photosensitive layer onto a conductive substrate and drying. The coating solution for the photosensitive layer is obtained by dissolving or dispersing a charge generator, an electron transport agent, a hole transport agent, a binder resin, filler particles, and components (for example, additives) added as necessary in a solvent. Manufactured.

  The solvent contained in the photosensitive layer coating solution is not particularly limited as long as each component contained in the coating solution can be dissolved or dispersed. Examples of solvents include alcohols (eg, methanol, ethanol, isopropanol or butanol), aliphatic hydrocarbons (eg, n-hexane, octane or cyclohexane), aromatic hydrocarbons (eg, benzene, toluene or xylene), Halogenated hydrocarbons (eg dichloromethane, dichloroethane, carbon tetrachloride or chlorobenzene), ethers (eg dimethyl ether, diethyl ether, tetrahydrofuran, ethylene glycol dimethyl ether, diethylene glycol dimethyl ether or propylene glycol monomethyl ether), ketones (eg acetone, Methyl ethyl ketone or cyclohexanone), esters (eg ethyl acetate or methyl acetate), dimethylformaldehyde, dimethylform Amide or dimethyl sulfoxide. These solvents are used alone or in combination of two or more. In order to improve the workability during the production of the photoreceptor, it is preferable to use a non-halogen solvent (a solvent other than the halogenated hydrocarbon) as the solvent.

  The coating solution is prepared by mixing each component and dispersing in a solvent. For mixing or dispersing, for example, a bead mill, a roll mill, a ball mill, an attritor, a paint shaker, or an ultrasonic disperser can be used.

  The photosensitive layer coating solution may contain, for example, a surfactant in order to improve the dispersibility of each component.

  The method for applying the photosensitive layer coating solution is not particularly limited as long as the coating solution can be uniformly applied onto the conductive substrate. Examples of the coating method include a dip coating method, a spray coating method, a spin coating method, and a bar coating method.

  The method for drying the photosensitive layer coating solution is not particularly limited as long as the solvent in the coating solution can be evaporated. For example, the method of heat-processing (hot-air drying) is mentioned using a high-temperature dryer or a vacuum dryer. The heat treatment conditions are, for example, a temperature of 40 ° C. or higher and 150 ° C. or lower and a time of 3 minutes or longer and 120 minutes or shorter.

  In addition, the manufacturing method of a photoreceptor may further include one or both of a step of forming an undercoat layer and a step of forming a protective layer as necessary. In the step of forming the undercoat layer and the step of forming the protective layer, a known method is appropriately selected.

<2. Image Forming Apparatus and Image Forming Method>
Next, the image forming apparatus 100 including the photoconductor 30 according to the present embodiment will be described with reference to FIG. An image forming method using the photoreceptor 30 according to the present embodiment will be described. FIG. 3 is a diagram illustrating an example of the configuration of the image forming apparatus 100, and the image forming apparatus 100 includes the photoreceptor 30 according to the present embodiment.

  The image forming apparatus 100 is not particularly limited as long as it is an electrophotographic image forming apparatus. For example, the image forming apparatus 100 may be a monochrome image forming apparatus or a color image forming apparatus. When the image forming apparatus 100 is a color image forming apparatus, the image forming apparatus 100 employs, for example, a tandem method. Hereinafter, the tandem image forming apparatus 100 will be described as an example.

  The image forming apparatus 100 may employ a direct transfer method or an intermediate transfer method. Hereinafter, the image forming apparatus 100 that employs the direct transfer method will be described as an example.

  The image forming apparatus 100 includes image forming units 40a, 40b, 40c, and 40d, a transfer belt 50, and a fixing unit 54. Hereinafter, when it is not necessary to distinguish, each of the image forming units 40a, 40b, 40c, and 40d is referred to as an image forming unit 40. When the image forming apparatus 100 is a monochrome image forming apparatus, the image forming apparatus 100 includes an image forming unit 40a, and the image forming units 40b to 40d are omitted.

  The image forming unit 40 includes a photoconductor 30, a charging unit 42, an exposure unit 44, a developing unit 46, and a transfer unit 48. A photoreceptor 30 is provided at the center position of the image forming unit 40. The photoconductor 30 is provided so as to be rotatable in the arrow direction (counterclockwise). Around the photoconductor 30, a charging unit 42, an exposure unit 44, a developing unit 46, and a transfer unit 48 are provided in order from the upstream side in the rotation direction of the photoconductor 30 with respect to the charging unit 42. The image forming unit 40 may further include a cleaning unit 52. When the cleaning unit 52 is provided, the charging unit 42, the exposure unit 44, the developing unit 46, the transfer unit 48, and the like around the photoconductor 30 in order from the upstream side in the rotation direction of the photoconductor 30 with respect to the charging unit 42 A cleaning unit 52 is provided. Further, the image forming unit 40 may further include a static elimination unit (not shown, for example, a static eliminator).

  The image forming method includes a charging step, an exposure step, a development step, and a transfer step. The image forming method may further include a cleaning step.

  In the charging step, the charging unit 42 charges the surface (specifically, the peripheral surface) of the photoreceptor 30 to a positive polarity. The photosensitive layer 32 (see FIG. 1) contains a compound (1) that is an electron transport agent and silica particles or resin particles that are filler particles. Therefore, there is a strong tendency that the photosensitive member 30 and the recording medium P are rubbed, and a minute component (for example, paper dust) of the recording medium P is positively charged. When the surface of the photoconductor 30 is charged to the positive polarity by the charging unit 42, the surface of the photoconductor 30 and the minute components of the recording medium P that are frictionally charged to the positive polarity are electrically repelled. As a result, the minute components of the recording medium P are difficult to adhere to the surface of the photoreceptor 30, and the occurrence of filming can be suitably suppressed.

  The charging unit 42 is a non-contact method or a contact method. An example of the non-contact charging unit 42 is a corotron charger or a scorotron charger. An example of the contact-type charging unit 42 is a charging roller or a charging brush.

  The charging unit 42 can charge the surface of the photoconductor 30 to a positive polarity while the charging unit 42 is in contact with the surface of the photoconductor 30. That is, the charging unit 42 can be a contact method.

  Normally, when the surface of the photoreceptor 30 is charged using a contact-type charging unit 42 (for example, a charging roller), the charging time is shorter than that of the non-contact type charging unit 42. The contact-type charging unit 42 has a short contact time with the surface of the photoconductor 30, and the contact-type charging unit 42 charges the photoconductor 30 within a short contact time. For this reason, the contact-type charging unit 42 tends to have a lower ability to charge the photoconductor 30 than the non-contact type charging unit 42. For this reason, the influence of the potential drop in the non-exposed area on the surface of the photoconductor 30 tends to remain, and a transfer memory tends to occur. However, the photoconductor 30 of this embodiment can suppress the generation of a transfer memory as already described. Therefore, even when the image forming apparatus 100 includes the contact-type charging unit 42, the generation of the transfer memory can be suitably suppressed.

  Further, in the image forming apparatus 100 including the contact-type charging unit 42, filming is likely to occur because minute components (for example, paper powder, toner, or external additives) attached to the surface of the photoreceptor 30 are fixed. . However, the photoconductor 30 of this embodiment can suppress the occurrence of filming as already described. Therefore, even when the image forming apparatus 100 includes the contact-type charging unit 42, the occurrence of filming can be suitably suppressed.

  As the contact charging unit 42, a charging roller can be preferably used. For example, the charging roller rotates following the rotation of the photoconductor 30 while contacting the surface of the photoconductor 30. For example, at least a surface portion of the charging roller is formed of a resin. The charging roller includes, for example, a core metal rotatably supported, a resin layer formed on the core metal, and a voltage applying unit that applies a voltage to the core metal. The charging unit 42, which is such a charging roller, charges the surface of the photoreceptor 30 that is in contact via the resin layer when the voltage application unit applies a voltage to the cored bar.

  The resin forming the resin layer of the charging roller is not particularly limited as long as the surface of the photoreceptor 30 can be charged satisfactorily. Specific examples of the resin contained in the resin layer are a silicone resin, a urethane resin, or a silicone-modified resin. The resin layer may contain an inorganic filler.

  In the exposure process, the exposure unit 44 exposes the surface of the charged photoreceptor 30. As a result, an electrostatic latent image is formed on the surface of the photoreceptor 30. The electrostatic latent image is formed based on image data input to the image forming apparatus 100.

  In the developing process, the developing unit 46 supplies toner to the electrostatic latent image formed on the photoreceptor 30. As a result, the electrostatic latent image is developed as a toner image. The photoreceptor 30 corresponds to an image carrier that carries a toner image. The toner may be used as a one-component developer. Alternatively, the toner and the desired carrier may be mixed and used in the two-component developer. When toner is used as a one-component developer, the developing unit 46 supplies toner that is a one-component developer to the electrostatic latent image formed on the photoreceptor 30. When the toner is used in the two-component developer, the developing unit 46 supplies toner out of the toner and the carrier contained in the two-component developer to the electrostatic latent image formed on the photoreceptor 30.

  Examples of toner supplied by the developing unit 46 are polymerized toner or pulverized toner. In the image forming apparatus 100, a polymerized toner can be used. Polymerized toner tends to have a high degree of circularity and a uniform particle size. When the image forming apparatus 100 includes the cleaning unit 52, the polymerized toner easily slips between the surface of the photoreceptor 30 and the cleaning unit 52. For this reason, the polymerized toner that has not been cleaned by the cleaning unit 52 remains on the surface of the photoconductor 30, and filming tends to occur. However, the photoconductor 30 of this embodiment can suppress the occurrence of filming as already described. Therefore, even when polymerized toner is used in the image forming apparatus 100, the occurrence of filming can be suitably suppressed.

  The polymerized toner is obtained, for example, by suspension polymerization, emulsion polymerization aggregation, dissolution suspension, or ester elongation polymerization. The polymerized toner has a spherical shape. The polymerized toner has a high degree of circularity. For example, the number average circularity of the polymerized toner is preferably 0.94 or more and 0.99 or less. An example of a method for measuring the number average circularity of the polymerized toner will be described. A sample (polymerized toner) 0.1 g and a dispersion liquid (sheath liquid) 20 mL are mixed to obtain a polymerized toner suspension. The number of polymerized toner particles contained in the obtained suspension and the circularity of each polymerized toner particle were measured using a flow-type particle image analyzer (“FPIA (registered trademark) -3000” manufactured by Sysmex Corporation). taking measurement. The sum of the measured circularity of the polymerized toner particles is divided by the number of measured polymerized toner particles. Thereby, the number average circularity of the polymerized toner particles is calculated.

  The transfer belt 50 conveys the recording medium P between the photoconductor 30 and the transfer unit 48. The transfer belt 50 is an endless belt. The transfer belt 50 is provided to be rotatable in the arrow direction (clockwise).

  In the transfer process, the transfer unit 48 transfers the toner image developed by the developing unit 46 from the photoreceptor 30 to the transfer target. When the image forming apparatus 100 employs the direct transfer method, the transfer target corresponds to the recording medium P. When the image forming apparatus 100 employs the direct transfer method, the photoconductor 30 is in contact with the recording medium P when the toner image is transferred from the photoconductor 30 to the recording medium P. The transfer unit 48 is, for example, a transfer roller.

  Usually, in an image forming apparatus that employs the direct transfer method, since the photosensitive member contacts the recording medium P, minute components of the recording medium P tend to adhere to the surface of the photosensitive member, and image defects due to filming occur. easy. However, as already described, the photoreceptor 30 of this embodiment is excellent in filming resistance. Therefore, even when the image forming apparatus 100 adopts the direct transfer method, the image forming apparatus 100 including the photoreceptor 30 can suppress the occurrence of image defects due to filming.

  Each of the image forming units 40a to 40d sequentially superimposes toner images of a plurality of colors (for example, four colors of black, cyan, magenta, and yellow) on the recording medium P on the transfer belt 50.

  A cleaning process may be performed after the transfer process. In the cleaning process, the cleaning unit 52 cleans the surface of the photoreceptor 30 after the toner image is transferred to the transfer target (corresponding to the recording medium P). The cleaning unit 52 cleans components remaining on the surface of the photoconductor 30 (hereinafter sometimes referred to as “residual components”). An example of the residual component is a toner component, and more specifically, a toner or a free external additive. Another example of the residual component is a non-toner component, and more specifically, a minute component (for example, paper dust) of the recording medium P.

  Each of the image forming units 40a, 40b, 40c, and 40d can include at least one cleaning unit 52. Examples of the cleaning unit 52 are a cleaning blade, a cleaning roller, a fur brush, an ultrasonic cleaning device, an air jet cleaning device, a magnetic brush cleaning device, or an electrostatic brush cleaning device.

  The cleaning unit 52 may be a cleaning blade. Since the cleaning blade presses minute components (for example, paper dust, toner, or external additives) adhering to the surface of the photoreceptor 30, filming is likely to occur on the surface of the photoreceptor 30. However, the photoconductor 30 of this embodiment can suppress the occurrence of filming as already described. Therefore, even when the image forming apparatus 100 includes a cleaning blade as the cleaning unit 52, the occurrence of filming can be suitably suppressed. When the image forming apparatus 100 includes a plurality of cleaning units 52, one of the plurality of cleaning units 52 may be a cleaning blade.

  The fixing unit 54 heats and / or pressurizes the unfixed toner image transferred to the recording medium P by the transfer unit 48. The fixing unit 54 is, for example, a heating roller and / or a pressure roller. The toner image is fixed on the recording medium P by heating and / or pressurizing the toner image. As a result, an image is formed on the recording medium P.

  The image forming apparatus 100 including the photoconductor 30 of the present embodiment has been described above with reference to FIG.

<3. Process cartridge>
With continued reference to FIG. 3, a process cartridge including the photoreceptor 30 of the present embodiment will be described. The process cartridge is an image forming cartridge. The process cartridge corresponds to each of the image forming units 40a to 40d. The process cartridge includes a photoreceptor 30. The process cartridge includes at least one selected from the group consisting of a charging unit 42, an exposure unit 44, a developing unit 46, and a transfer unit 48 in addition to the photoreceptor 30. The process cartridge may further include a cleaning unit 52. The process cartridge may further include a static elimination unit (not shown). However, the process cartridge may employ a static elimination-less method. The process cartridge is designed to be detachable from the image forming apparatus 100. Therefore, the process cartridge is easy to handle, and when the sensitivity characteristic of the photoconductor 30 is deteriorated, the process cartridge including the photoconductor 30 can be easily and quickly replaced. The process cartridge including the photoconductor 30 of the present embodiment has been described above with reference to FIG.

  Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not limited to the scope of the examples.

<Preparation of electron transport agent>
Each of the compounds (1-1) to (1-9), which are electron transport agents for inclusion in the photosensitive layer, was prepared by the following method.

(Production of Compound (1-1))
Compound (1-1) was produced according to reactions (R-3) and (R-4).

  In reaction (R-3), compound (A-1) and compound (B-1) were reacted to obtain compound (C-1). Hereinafter, the compound (A-1) may be referred to as a first raw material for the reaction (R-3), and the compound (B-1) may be referred to as a second raw material for the reaction (R-3). 2.24 g (0.01 mol) of compound (A-1), 3.26 g (0.03 mol) of compound (B-1) and toluene (100 mL) were added to the flask to dissolve the contents of the flask. . P-Toluenesulfonic acid (0.001 mol) was added into the flask. The flask was set in a Dean-Stark apparatus. The contents of the flask were refluxed at 90 ° C. for 5 hours while dehydrating. The contents of the obtained flask were decompressed, and toluene was distilled off. Ion exchange water was added to the mixture after distillation under reduced pressure, and the mixture was extracted with chloroform. After the obtained organic layer was dried, the organic layer was depressurized and chloroform was distilled off. As a result, compound (C-1) was obtained as a crude product. The yield of compound (C-1) was 2.84 g, and the yield of compound (C-1) from compound (A-1) was 90 mol%.

  In reaction (R-4), compound (C-1) and compound (D, malononitrile) were reacted to obtain compound (1-1). Hereinafter, the compound (C-1) may be referred to as a first raw material for the reaction (R-4) and the compound (D) may be referred to as a second raw material for the reaction (R-4). 1.57 g (0.005 mol) of compound (C-1) and 0.66 g (0.01 mol) of compound (D) were added to methanol (100 mL) to obtain a methanol solution. To the methanol solution, 0.08 g (0.001 mol) of piperidine was added to obtain a mixture. The mixture was stirred at 80 ° C. for 3 hours at reflux. Subsequently, the mixture was added to ion exchange water (200 mL) to precipitate a solid, and the solid was collected by filtration. The obtained solid was purified by silica gel column chromatography using chloroform as a developing solvent. As a result, compound (1-1) was obtained. The yield of compound (1-1) was 1.45 g, and the yield of compound (1-1) from compound (C-1) was 80 mol%.

(Production of compounds (1-2) to (1-9))
The reaction (R-3) was carried out in the same manner as in the production of the compound (C-1) except that the following points were changed. Subsequently, reaction (R-4) was carried out in the same manner as in the production of compound (1-1) except that the following points were changed. As a result, compounds (1-2) to (1-9) were obtained.

  The 1st raw material of reaction (R-3) was changed into the 1st raw material shown in Table 2 from the compound (A-1) in manufacture of a compound (C-1). The 2nd raw material of reaction (R-3) was changed into the 2nd raw material shown in Table 2 from the compound (B-1) in manufacture of a compound (C-1). The addition mass of the second raw material in the reaction (R-3) was changed from 3.26 g in the production of the compound (C-1) to the addition mass of the second raw material shown in Table 2. In addition, the number of moles of each raw material used in the production of the compounds (C-2) to (C-9) was the same as the number of moles of the corresponding raw material used in the production of the compound (C-1). . As a result, compounds (C-2) to (C-9) were obtained as reaction products of reaction (R-3) instead of compound (C-1). Table 2 shows the yields of the compounds (C-2) to (C-9) obtained in the reaction (R-3). In addition, Table 2 shows the yields of the compounds (C-2) to (C-9) from the first raw material of the reaction (R-3).

  Compounds (A-1) to (A-3), (B-1) to (B-3), (B-5) to (B-9) and (C-1) to (C-) in Table 2 Each of 9) has the following chemical formulas (A-1) to (A-3), (B-1) to (B-3), (B-5) to (B-9) and (C-1) It is a compound represented by-(C-9).

  Next, the 1st raw material of reaction (R-4) was changed into the 1st raw material shown in Table 3 from the compound (C-1) in manufacture of a compound (1-1). The addition mass of the first raw material in the reaction (R-4) was changed from 1.57 g in the production of the compound (1-1) to the addition mass of the first raw material shown in Table 3. In addition, the number of moles of each raw material used in the production of the compounds (1-2) to (1-9) is the same as the number of moles of the corresponding raw material used in the production of the compound (1-1). As a result, as the reaction product of reaction (R-4), compounds (1-2) to (1-9) as final target compounds were obtained instead of compound (1-1). Table 3 shows the yields of the compounds (1-2) to (1-9) obtained by the reaction (R-4). In addition, Table 3 shows the yields of the compounds (1-2) to (1-9) from the first raw material of the reaction (R-4).

Next, with reference to ¹ H-NMR (proton nuclear magnetic resonance spectroscopy), it was analyzed by ¹ H-NMR spectrum of the compound prepared (1-1) to (1-9). The magnetic field strength was set to 300 MHz. Deuterated chloroform (CDCl ₃ ) was used as the solvent. Tetramethylsilane (TMS) was used as an internal standard substance.

As representative examples of the compounds (1-1) to (1-9), the chemical shift values of ¹ H-NMR spectra of the compounds (1-1), (1-3) and (1-4) are as follows: Show. In addition, ¹ H-NMR spectra of the compounds (1-3) and (1-4) are shown in FIGS. 4 and 5, respectively. From the measured ¹ H-NMR spectrum and chemical shift value, it was confirmed that each of the compounds (1-1), (1-3) and (1-4) was obtained. As for other compounds (1-2) and (1-5) to (1-9), from the measured ¹ H-NMR spectrum and chemical shift value, compounds (1-2) and (1-5) to (1) It was confirmed that each of (1-9) was obtained.

Compound (1-1): ¹ H-NMR (300 MHz, CDCl ₃ ) δ = 8.53 (dd, 1H), 8.39 (d, 1H), 8.18 (d, 1H), 7.85 ( dd, 1H), 7.49 (dt, 1H), 7.35 (t, 1H), 7.34 (dt, 1H), 4.45 (t, 2H), 3.63 (t, 2H), 1.90-2.07 (m, 4H).

Compound (1-3): ¹ H-NMR (300 MHz, CDCl ₃ ) δ = 8.62 (dd, 1H), 8.46 (d, 1H), 8.21 (d, 1H), 7.92 ( dd, 1H), 7.53 (dt, 1H), 7.35-7.45 (m, 2H), 4.69-4.85 (m, 2H), 4.38-4.47 (m, 1H), 3.80-3.93 (m, 2H).

Compound (1-4): ¹ H-NMR (300 MHz, CDCl ₃ ) δ = 8.30 (d, 1H), 7.68-7.72 (m, 2H), 7.47-7.60 (m , 3H), 7.36 (dt, 1H), 4.47 (t, 2H), 3.62 (t, 2H), 1.90-2.03 (m, 4H).

<Material of photoconductor>
The following charge generator, hole transport agent, electron transport agent, binder resin and filler particles were prepared as materials for forming the photosensitive layer of the photoreceptor.

(Charge generator)
As the charge generator, a charge generator (CGM1) which is Y-type titanyl phthalocyanine was used. The charge generator (CGM1, Y-type titanyl phthalocyanine) has a Bragg angle of 2θ ± 0.2 ° = 9.2 °, 14.5 °, 18.1 °, 24.1 ° in the CuKα characteristic X-ray diffraction spectrum chart. 27.2 ° and the main peak was 27.2 °. The CuKα characteristic X-ray diffraction spectrum was measured using the measurement apparatus and measurement conditions described in the embodiment.

  As the charge generating agent, a charge generating agent (CGM2) which is X-type metal-free phthalocyanine was used.

  As the charge generator, a charge generator (CGM3) which is α-type titanyl phthalocyanine was used. The charge generating agent (CGM3, α-type titanyl phthalocyanine) has a Bragg angle 2θ ± 0.2 ° = 7.5 °, 10.2 °, 12.6 °, 13.2 ° in the CuKα characteristic X-ray diffraction spectrum chart. It has peaks at 15.1 °, 16.3 °, 17.3 °, 18.3 °, 22.5 °, 24.2 °, 25.3 °, 28.6 °, and the main peak is It was 28.6 °. The CuKα characteristic X-ray diffraction spectrum was measured using the measurement apparatus and measurement conditions described in the embodiment.

(Hole transport agent)
The compounds (HTM1-1), (HTM2-1), (HTM2-2), (HTM4-1) and (HTM6-1) described in the embodiment were prepared.

(Electron transfer agent)
As the electron transport agent, compounds (1-1) to (1-9) obtained by preparing the electron transport agent were prepared.

  As electron transporting agents, compounds represented by chemical formulas (ETM-A) and (ETM-B) (hereinafter sometimes referred to as compounds (ETM-A) and (ETM-B), respectively) were also prepared.

(Binder resin)
As binder resins, the polycarbonate resins (PC-1) to (PC-5) described in the embodiments (viscosity average molecular weights: 50000, 48500, 49800, 50000, 50000, respectively) and polyarylate resins (PAR-1) (viscosity average) Molecular weight 50000) was prepared.

(Filler particles)
The filler particles (F1), (F3), (F4), (F6), (F7), (F9), and (F10) described in the embodiment were prepared as the filler particles.

As filler particles, filler particles (F11) (“NanoTek Al ₂ O ₃ ” manufactured by CI Kasei Co., Ltd., metal particles, filler material: alumina, volume median diameter: 0.030 μm) were also prepared.

<Manufacture of photoconductor>
Photoconductors (P-A1) to (P-A32) and photoconductors (P-B1) to (P-B4) were produced using materials for forming the photosensitive layer. Photoconductors (P-A1) to (P-A32) are examples, and photoconductors (P-B1) to (P-B4) are comparative examples.

(Manufacture of photoconductor (P-A1))
3 parts by weight of a charge generating agent (CGM1), 60 parts by weight of a compound (HTM1-1) as a hole transporting agent, 40 parts by weight of a compound (1-1) as an electron transporting agent, 5 parts by weight of filler particles (F7), 100 parts by mass of polycarbonate resin (PC-1) as a binder resin and 800 parts by mass of tetrahydrofuran as a solvent were added to the container. The material in the container and the solvent were mixed for 2 minutes using a rod-like acoustic oscillator, and the material was dispersed in the solvent. Further, using a ball mill, the material in the container and the solvent were mixed for 50 hours to disperse the material in the solvent. This obtained the coating liquid for photosensitive layers. The photosensitive layer coating solution was coated on an aluminum drum-shaped support as a conductive substrate using a dip coating method. The applied photosensitive layer coating solution was dried with hot air at 100 ° C. for 40 minutes. As a result, a photosensitive layer (film thickness: 25 μm) was formed on the conductive substrate. As a result, a photoreceptor (P-A1) was obtained. In the photoreceptor (P-A1), the conductive substrate had an oxide coating, and the photosensitive layer was indirectly disposed on the conductive substrate via the oxide coating.

(Production of photoconductors (P-A2) to (P-A32) and (P-B1) to (P-B4))
Photoconductors (P-A2) to (P-A32) and (P-B1) to (P-A1) are the same as the production of the photoconductor (P-A1) except that the following points (1) to (7) are changed. Each of (P-B4) was manufactured.
(1) Although the charge generating agent (CGM1) was used in the production of the photoreceptor (P-A1), the photoreceptors (P-A2) to (P-A32) and (P-B1) to (P-B4) In each production, charge generators of the types shown in Tables 4 to 6 were used.
(2) In the production of the photoreceptor (P-A1), the compound (HTM1-1) was used as the hole transport agent, but the photoreceptors (P-A2) to (P-A32) and (P-B1) to (P In each production of P-B4), hole transport agents of the types shown in Tables 4 to 6 were used.
(3) In the production of the photoreceptor (P-A1), the compound (1-1) was used as an electron transfer agent, but the photoreceptors (P-A2) to (P-A32) and (P-B1) to (P In each production of -B4), electron transport agents of the types shown in Tables 4 to 6 were used.
(4) In the production of the photoconductor (P-A1), 40 parts by mass of an electron transfer agent was added, but the photoconductors (P-A2) to (P-A32) and (P-B1) to (P-B4) In each production, the amount of electron transport agent shown in Tables 4 to 6 was added.
(5) In the production of the photoreceptor (P-A1), filler particles (F7) were used as filler particles. However, the photoreceptors (P-A2) to (P-A32) and (P-B1) to (P-B4) were used. In each production of), filler particles of the types shown in Tables 4 to 6 were used.
(6) In the production of the photoreceptor (P-A1), 5 parts by mass of filler particles were added. Each of the photoreceptors (P-A2) to (P-A32) and (P-B1) to (P-B4) was used. In the production, filler particles in the amounts shown in Tables 4 to 6 were added.
(7) In the production of the photoreceptor (P-A1), polycarbonate resin (PC-1) was used as the binder resin, but the photoreceptors (P-A2) to (P-A32) and (P-B1) to (P In each production of -B4), binder resins of the types shown in Tables 4 to 6 were used.

<Evaluation of transfer memory suppression>
It was evaluated whether or not the generation of the transfer memory was suppressed for each of the photoreceptors (P-A1) to (P-A32) and (P-B1) to (P-B4). Whether or not the generation of the transfer memory is suppressed was evaluated in an environment of a temperature of 10 ° C. and a relative humidity of 20% RH.

  First, the photoconductor was mounted on an evaluation machine. A color printer (“FS-C5250DN” manufactured by Kyocera Document Solutions Inc.) was used as an evaluation machine. This evaluator was provided with a contact charging type charging roller as a charging portion. In addition, the potential at which the charging roller charges the surface of the photoconductor was set to positive polarity (+600 V). This evaluator was provided with a direct transfer type transfer section. This evaluator was provided with a cleaning blade as a cleaning unit. Toner (polymerized toner as a one-component developer, prototype, number average circularity of 0.95) was put into a toner container of an evaluation machine.

  Image I (pattern image with a printing rate of 4%) was printed on 1000 sheets of paper (A4 size paper) at intervals of 15 seconds using an evaluator. After the image I was printed on 1000 sheets, the evaluation image was printed on one sheet. The evaluation image will be described later with reference to FIG. Next, the printed evaluation image was observed with the naked eye to confirm the presence or absence of an image ghost. The image ghost will be described later with reference to FIG. When a transfer memory is generated on the photoconductor, an image ghost (particularly a negative ghost) is generated on the formed image. Based on the confirmation result of the image ghost, whether or not the generation of the transfer memory is suppressed is evaluated according to the following criteria. The evaluation results are shown in Tables 4-6. The photoconductors having evaluations A to C were evaluated as having suppressed generation of transfer memory.

  The evaluation image 70 will be described with reference to FIG. FIG. 6 is a diagram showing the evaluation image 70. The evaluation image 70 includes a first area 72 and a second area 74. The first area 72 is an area corresponding to one rotation of the photoreceptor. The first area 72 includes a first image 76. The first image 76 is composed of a donut-shaped solid image (image density 100%). This solid image is composed of a set of two concentric circles. The second area 74 is an area corresponding to one rotation of the photoreceptor. The second area 74 includes a second image 78. The second image 78 is composed of an entire halftone image (image density 40%). First, the first image 76 of the first region 72 was formed, and then the second image 78 of the second region 74 was formed. The first image 76 is an image corresponding to one rotation of the photoconductor, and the second image 78 is an image corresponding to one rotation of the next rotation on the basis of the rotation forming the first image 76.

  An image 60 in which an image ghost has occurred will be described with reference to FIG. FIG. 7 is a diagram illustrating an image 60 in which an image ghost has occurred. The image 60 includes a first area 72 and a third area 64. The third area 64 includes a fourth area 68 and a fifth area 69. In the image 60, the second image 78 (entire halftone image having an image density of 40%) is to be formed in the second region 74 as shown in FIG. 6, but the image is shown in the third region 64 as shown in FIG. A ghost appears. Specifically, a fourth region 68 and a fifth region 69 appear in the third region 64. The image density of the fifth area 69 is higher than that of the fourth area 68. The image density of the fifth region 69 is higher than the set image density. The fifth area 69 is an area corresponding to the non-exposed area of the first area 72. As described above, the evaluation image 70 and the image 60 in which the image ghost has occurred have been described with reference to FIGS.

(Evaluation criteria for transfer memory suppression)
Evaluation A: No image ghost was observed.
Evaluation B: A slight image ghost was observed.
Evaluation C: Although an image ghost was observed, it was a level with no practical problem.
Evaluation D: Image ghost was clearly observed, and was a practically problematic level.

<Evaluation of filming resistance>
It was evaluated whether or not the occurrence of filming was suppressed for each of the photoreceptors (P-A1) to (P-A32) and (P-B1) to (P-B4). Whether filming was suppressed or not was evaluated in an environment of a temperature of 10 ° C. and a relative humidity of 15% RH. The evaluation machine and toner used in the evaluation of filming resistance were the same as the evaluation machine and toner used in the evaluation of transfer memory suppression.

  First, the photoconductor was mounted on an evaluation machine. An image II (print pattern image with an image density of 1%) was printed on 5000 sheets of paper (A4 size paper) at intervals of 15 seconds using an evaluation machine. After printing image II on 5000 sheets of paper, image III was printed on a single sheet of paper. The image III was an entire gray image (image density 50%).

  The obtained image III was observed with the naked eye to confirm the presence or absence of muscles and dash marks. When filming occurs on the photoconductor, streaks and dashes are generated on the formed image. The streak is an image defect in which a black line parallel to the direction in which the image is printed appears. A dash mark is an image defect in which black dots arranged parallel to the direction in which the image is printed appear. Based on the confirmation results of the streaks and the dash marks, it was evaluated whether the occurrence of filming was suppressed according to the following criteria. The evaluation results are shown in Tables 4-6. The photoreceptors with evaluations A to C were evaluated as having suppressed filming.

(Filming resistance evaluation criteria)
Evaluation A: Neither a streak nor a dash mark was confirmed.
Evaluation B: Minor streaks and dash marks were slightly confirmed.
Evaluation C: Minor streaks and dash marks were confirmed. However, it was a level with no practical problems.
Evaluation D: Streaks and dash marks were clearly confirmed, and there was a problem in practical use.

<Evaluation of sensitivity characteristics>
The sensitivity characteristics of the photoreceptors were evaluated for each of the photoreceptors (P-A1) to (P-A32) and (P-B1) to (P-B4). The sensitivity characteristics of the photoconductor were evaluated in an environment at a temperature of 23 ° C. and a relative humidity of 50% RH. First, the surface of the photosensitive member was charged to +600 V using a drum sensitivity tester (manufactured by Gentec Corporation). Next, monochromatic light (wavelength 780 nm, light energy 0.6 μJ / cm ² ) was extracted from the white light of the halogen lamp using a bandpass filter. The surface of the photoreceptor was irradiated with the extracted monochromatic light. The surface potential of the photoconductor was measured after 50 milliseconds had elapsed from the end of irradiation. The measured surface potential was defined as a sensitivity potential (V _L , unit: + V). Tables 4 to 6 show the measured sensitivity potential (V _L ) of the photoreceptor. It should be noted that the smaller the sensitivity potential (V _L ), the better the sensitivity characteristics of the photoreceptor.

In Tables 4 to 6, CGM, HTM, ETM, resin, part, and _VL represent a charge generating agent, a hole transporting agent, an electron transporting agent, a binder resin, a mass part, and a sensitivity potential, respectively. “F7 / F1” and “2.5 / 2.5” in Example 30 of Table 5 used 2.5 parts by mass of filler particles (F7) and 2.5 parts by mass of filler particles (F1). It shows that. “1-1 / 1-7” and “20/20” in Example 31 of Table 6 indicate that 20 parts by mass of the compound (1-1) and 20 parts by mass of the compound (1-7) were used. Show. “PC-1 / PC-5” and “50/50” in Example 32 of Table 6 used 50 parts by mass of polycarbonate resin (PC-1) and 50 parts by mass of polycarbonate resin (PC-5). It shows that.

  In the photoreceptors (P-A1) to (P-A32), the photosensitive layer contained a charge generating agent, a hole transport agent, an electron transport agent, a binder resin, and filler particles. The filler particles were at least one of silica particles and resin particles. Specifically, the photosensitive layer contained at least one of filler particles (F1), (F3), (F4), (F6), (F7), (F9) and (F10). The electron transfer agent was at least one compound (1). Specifically, the photosensitive layer contained at least one of compounds (1-1) to (1-9) as an electron transport agent. Therefore, as is apparent from Tables 4 to 6, in the photoconductors (P-A1) to (P-A32), the evaluation of the transfer memory suppression was A to C, and the generation of the transfer memory was suppressed. In the photoreceptors (P-A1) to (P-A32), the evaluation of filming resistance was A to C, and the occurrence of filming was suppressed. Further, as is apparent from Tables 4 to 6, in the photoconductors (P-A1) to (P-A32), the sensitivity characteristics of the photoconductors are maintained, the filming resistance is improved, and the transfer memory is generated. Was suppressed.

  On the other hand, in the photoreceptor (P-B1), the photosensitive layer did not contain filler particles. In each of the photoreceptors (P-B2) and (P-B3), the photosensitive layer did not contain the compound (1) as an electron transport agent. Specifically, the photosensitive layer of the photoreceptor (P-B2) contained a compound (ETM-A) as an electron transfer agent, but the compound (ETM-A) is a compound represented by the general formula (1). It wasn't. The photosensitive layer of the photoreceptor (P-B3) contained the compound (ETM-B) as an electron transfer agent, but the compound (ETM-B) was not a compound represented by the general formula (1). . In the photoreceptor (P-B4), the filler particles contained in the photosensitive layer were metal particles instead of silica particles and resin particles. Therefore, as is clear from Table 6, in the photoconductors (P-B1) to (P-B4), the evaluation of the transfer memory suppression was D, and the transfer memory was clearly generated. In the photoreceptors (P-B1) to (P-B4), the evaluation of filming resistance was D, and filming was clearly generated.

  From the above, it has been shown that the photoconductor according to the present invention can improve the filming resistance and suppress the generation of the transfer memory. Further, it has been shown that the process cartridge and the image forming apparatus according to the present invention can improve the filming resistance and suppress the generation of the transfer memory. Further, according to the image forming method of the present invention, it has been shown that a good image can be formed by using a photoconductor capable of improving the filming resistance and suppressing the generation of a transfer memory.

  The photoreceptor according to the present invention can be used in an image forming apparatus.

30 Electrophotographic photoreceptor 31 Conductive substrate 32 Photosensitive layer 33 Subbing layer 42 Charging unit 44 Exposure unit 46 Development unit 48 Transfer unit 52 Cleaning unit 100 Image forming apparatus P Recording medium

Claims (23)

An electrophotographic photosensitive member comprising a conductive substrate and a photosensitive layer,
The photosensitive layer is a single layer,
The photosensitive layer includes a charge generator, a hole transport agent, an electron transport agent, a binder resin, and filler particles,
The filler particles are at least one of silica particles and resin particles,
The electron transport agent is an electrophotographic photosensitive member containing at least one compound represented by the general formula (1).

In the general formula (1), R ₁ is
An alkyl group having 1 or more and 8 or less carbon atoms having one or two halogen atoms,
An aryl group having 6 to 14 carbon atoms, which may have one or two halogen atoms and may have an alkyl group having 1 to 6 carbon atoms,
A 5- to 14-membered heterocyclic group having 1 or 2 halogen atoms, or
It represents an aralkyl group having 7 or more and 20 or less carbon atoms having one or two halogen atoms . The compound represented by the general formula (1) has chemical formulas (1-1), (1-2), (1-3), (1-4), (1-5), (1-6), The electrophotographic photosensitive member according to claim 1, which is a compound represented by (1-7), (1-8) or (1-9).

The volume median diameter of the filler particles is 5nm or more 10μm or less, the electrophotographic photosensitive member according to claim 1 or 2. The content of the filler particles is at most 30 parts by mass or more 0.5 part by weight per 100 parts by weight of the binder resin of the electrophotographic photosensitive member according to any one of claims 1-3. The filler particles are the resin particles,
The electrophotographic photoreceptor according to any one of claims 1 to 4 , wherein the resin particles are silicone resin particles, polyphenylene sulfide resin particles, or polytetrafluoroethylene resin particles. The filler particles are the resin particles,
The resin particles contain a fluorine atom, an electrophotographic photosensitive member according to any one of claims 1-5. The charge generating agent is a metal-free phthalocyanine or metal phthalocyanine, electrophotographic photosensitive member according to any one of claims 1-6. The charge generating agent is metal phthalocyanine;
The metal phthalocyanine is a titanyl phthalocyanine crystal;
The titanyl phthalocyanine crystal has a main peak at 27.2 ° of Bragg angles (2θ ± 0.2 °) in CuKα characteristic X-ray diffraction spectrum, the electrophotographic photosensitive according to any one of claims 1-7 body. The binder resin according to any one of claims 1 to 8 , wherein the binder resin includes at least one resin having at least one of a repeating unit represented by the general formula (2) and a repeating unit represented by the general formula (3). The electrophotographic photosensitive member according to Item.

In the general formula (2),
R ¹¹ and R ¹² represent a hydrogen atom, an alkyl group having 1 to 6 carbon atoms which may have a halogen atom, or a phenyl group which may have a substituent,
R ¹¹ and R ¹² may be bonded to each other to represent a cycloalkylidene group,
R ¹¹ and R ¹² may be the same or different from each other;
R ¹³ and R ¹⁴ represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms which may have a halogen atom,
R ¹³ and R ¹⁴ may be the same or different from each other;
In the general formula (3),
R ¹⁵ and R ¹⁶ represent a hydrogen atom, an alkyl group having 1 to 6 carbon atoms which may have a halogen atom or a phenyl group which may have a substituent,
R ¹⁵ and R ¹⁶ may be bonded to each other to represent a cycloalkylidene group,
R ¹⁵ and R ¹⁶ may be the same or different from each other;
R ¹⁷ and R ¹⁸ represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms which may have a halogen atom,
R ¹⁷ and R ¹⁸ may be the same or different from each other. The resin having at least one of the repeating unit represented by the general formula (2) and the repeating unit represented by the general formula (3) is a polycarbonate resin having a repeating unit represented by the general formula (2). The electrophotographic photosensitive member according to claim 9 , which is a polyarylate resin having a repeating unit represented by the general formula (3). In the general formula (2),
R ¹¹ and R ¹² represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, or R ¹¹ and R ¹² represent a cycloalkylidene group having 5 to 7 carbon atoms bonded to each other,
R ¹³ and R ¹⁴ represent a hydrogen group or a methyl group which may have a halogen atom,
R ¹³ and R ¹⁴ are the same as each other;
In the general formula (3),
R ¹⁵ and R ¹⁶ represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms,
R ¹⁵ and R ¹⁶ are different from each other;
R ¹⁷ and R ¹⁸ represent an alkyl group having 1 to 3 carbon atoms,
The electrophotographic photosensitive member according to claim 9 or 10 , wherein R ¹⁷ and R ¹⁸ are the same as each other. The polycarbonate resin having the repeating unit represented by the general formula (2) is represented by the chemical formula (PC-1), (PC-2), (PC-3), (PC-4) or (PC-5). A polycarbonate resin having a repeating unit,
The electrophotographic photosensitive resin according to claim 10 or 11 , wherein the polyarylate resin having a repeating unit represented by the general formula (3) is a polyarylate resin having a repeating unit represented by the chemical formula (PAR-1). body.

Content of the filler particles is 3 parts by mass or more and 10 parts by mass or less with respect to 100 parts by mass of the binder resin.
The filler particles are the resin particles,
The resin particles contain fluorine atoms,
The binder resin is a polycarbonate resin having a repeating unit represented by the chemical formula (PC-1) or (PC-3),
Compound represented by the general formula (1) has the formula (1-1), (1-3), a compound represented by (1-7) or (1-9), according to claim 1 to 12 The electrophotographic photosensitive member according to any one of the above.

The hole transport agent has the general formula (HTM1), (HTM2), (HTM3), (HTM4), (HTM5), (HTM6) or a compound represented by (HTM7), according to claim 1 to 13 The electrophotographic photosensitive member according to any one of the above.

In the general formula (HTM1),
Q ⁸ , Q ¹⁰ , Q ¹¹ , Q ¹² , Q ¹³ and Q ¹⁴ are each independently a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or a phenyl group. Represents
Q ⁹ and Q ¹⁵ each independently represents an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or a phenyl group,
b represents an integer of 0 to 5,
c represents an integer of 0 or more and 4 or less,
k represents 0 or 1.

In the general formula (HTM2),
Q ¹ represents a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or a phenyl group that may have an alkyl group having 1 to 6 carbon atoms,
Two Q ¹ may be the same or different from each other,
Q ² represents an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or a phenyl group,
Q ³ , Q ⁴ , Q ⁵ , Q ⁶ and Q ⁷ each independently represent a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or a phenyl group, Two adjacent ones of Q ³ , Q ⁴ , Q ⁵ , Q ⁶ and Q ⁷ may be bonded to each other to represent a ring;
a represents an integer of 0 to 5,
t and u each independently represents an integer of 0 or more and 2 or less.

In the general formula (HTM3),
Q ¹⁶ , Q ¹⁷ , Q ¹⁸ and Q ¹⁹ each independently represents an alkyl group having 1 to 4 carbon atoms.

In the general formula (HTM4),
Q ²⁰ , Q ²¹ , Q ²² and Q ²³ each independently represents an alkyl group having 1 to 4 carbon atoms,
v1, v2, v3 and v4 each independently represent an integer of 0 or more and 5 or less.

In the general formula (HTM5),
R ^d , R ^e and R ^f each independently represents an alkyl group having 1 to 6 carbon atoms,
o, p, and r each independently represent an integer of 0 or more and 5 or less.

In the general formula (HTM6),
R ^a , R ^b and R ^c each independently represents an alkyl group having 1 to 6 carbon atoms, a phenyl group or an alkoxy group having 1 to 6 carbon atoms,
q represents an integer of 0 or more and 4 or less,
s and n each independently represent an integer of 0 or more and 5 or less.

In the general formula (HTM7),
Q ³¹ , Q ³³ and Q ³⁵ each independently represents an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms or a phenyl group,
Q ³² , Q ³⁴ and Q ³⁶ are each independently a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms or an alkyl group having 1 to 6 carbon atoms. Represents a phenyl group which may be substituted;
d, e and f each independently represent 0 or 1,
g, h and i each independently represents an integer of 0 or more and 5 or less. The electrophotographic photoreceptor according to claim 14 , wherein the hole transport agent includes a compound represented by the general formula (HTM1), (HTM2), (HTM4), or (HTM6). The photosensitive layer, wherein either disposed directly on the conductive substrate, or an undercoat layer or via the oxide film is disposed, an electrophotographic photosensitive member according to any one of claims 1 to 15. A process cartridge comprising the electrophotographic photosensitive member according to any one of claims 1 to 16 . An image forming apparatus comprising the electrophotographic photosensitive member according to any one of claims 1 to 16 , a charging unit, an exposure unit, a developing unit, and a transfer unit,
The charging unit charges the surface of the electrophotographic photosensitive member to a positive polarity,
The exposing unit exposes the charged surface of the electrophotographic photosensitive member to form an electrostatic latent image on the surface of the electrophotographic photosensitive member;
The developing unit supplies toner to the electrostatic latent image, develops the electrostatic latent image as a toner image,
The transfer unit is an image forming apparatus that transfers the toner image from the electrophotographic photosensitive member to a transfer target. The transfer object is a recording medium,
19. The image forming apparatus according to claim 18 , wherein the electrophotographic photosensitive member is in contact with the recording medium when the transfer unit transfers the toner image from the electrophotographic photosensitive member to the recording medium. The image forming apparatus according to claim 18 or 19 , wherein the charging unit charges the surface of the electrophotographic photosensitive member to a positive polarity while the charging unit is in contact with the surface of the electrophotographic photosensitive member. A cleaning unit;
The cleaning unit cleans the surface of the electrophotographic photosensitive member on which the toner image is transferred to the transfer target;
The image forming apparatus according to any one of claims 18 to 20 , wherein the cleaning unit is a cleaning blade. The image forming apparatus according to any one of claims 18 to 21 , wherein the toner is a polymerized toner. A charging step for charging the surface of the electrophotographic photosensitive member according to any one of claims 1 to 16 to a positive polarity,
Exposing the surface of the charged electrophotographic photosensitive member to form an electrostatic latent image on the surface of the electrophotographic photosensitive member; and
A developing step of supplying polymerized toner to the electrostatic latent image and developing the electrostatic latent image as a toner image;
A transfer step of transferring the toner image from the electrophotographic photosensitive member to a transfer target.

Images