JP5481826B2 - Electrophotographic photosensitive member production coating liquid, electrophotographic photosensitive member, image forming apparatus, and electrophotographic photosensitive member cartridge - Google Patents

Description

  The present invention relates to a coating liquid for producing an electrophotographic photoreceptor, an electrophotographic photoreceptor, an image forming apparatus produced using the photoreceptor, and an electrophotographic photoreceptor cartridge.

  The electrophotographic technique is widely used in the fields of copiers, various printers, printing machines, etc. because it is excellent in immediacy and provides high-quality images. As an electrophotographic photoreceptor that is the core of electrophotographic technology, an electrophotographic photoreceptor using an organic photoconductive material (hereinafter simply referred to as “photosensitive material”) that has advantages such as non-pollution, easy film formation, and easy manufacture. Also referred to as "body").

  As an electrophotographic photoreceptor using an organic photoconductive material, a so-called dispersion type single-layer photoreceptor in which a photoconductive fine powder is dispersed in a binder resin, a charge generation layer and a charge transport layer are laminated. Multilayer photoreceptors are known. Multilayer photoconductors can provide highly sensitive and stable photoconductors by combining high-efficiency charge generation materials and charge transport materials in separate layers, and combining them with the most suitable ones. Photoconductors that are easy to adjust are obtained, and the photosensitive layer can be easily formed by coating, has high productivity, and is advantageous in terms of cost. Yes.

  On the other hand, the single-layer type photoconductor is slightly inferior to the multilayer type photoconductor in terms of electrical characteristics and the degree of freedom of material selection is somewhat small, but it can generate charges near the surface of the photoconductor, so it has high resolution. In addition, there is an advantage that a high printing durability can be achieved by increasing the thickness of the film because the image is not blurred even if the thickness is increased. In addition, the single-layer type photoreceptor is advantageous in that there are few coating steps and is advantageous for interference fringes and tube defects derived from a conductive substrate (support), and an inexpensive substrate such as a non-cutting tube can be used. For this reason, there is an advantage that the cost can be reduced.

  Further, since the electrophotographic photosensitive member is repeatedly used in an electrophotographic process, that is, a cycle such as charging, exposure, development, transfer, cleaning, and static elimination, it is deteriorated by various stresses during that time. Among these, as chemical deterioration, for example, strong oxidizing ozone or NOx generated from a corona charger usually used as a charger can damage the photosensitive layer. Deterioration of electrical stability, such as a decrease in image quality and an increase in residual potential, and image defects associated therewith may occur. These are largely derived from chemical deterioration of the charge transport material contained in the photosensitive layer.

  Furthermore, with the recent increase in the speed of the electrophotographic process, it is essential to increase the sensitivity and response of the electrophotographic photosensitive member. Of these, in order to achieve high sensitivity, it is necessary not only to optimize charge generation materials, but also to develop charge transport materials with good matching with them. There is a need to develop charge transport materials that exhibit sensitivity and a sufficiently low residual potential upon exposure.

  One of charge transport materials that can handle high speed and high image quality in recent years is an enamine compound. For example, it is stated that the enamine compounds described in Patent Documents 1 to 3 can be suitably used for electrophotographic photoreceptor applications. However, the enamine-based compound has a feature that the stability of the compound in the solution is low, and it easily hydrolyzes in the coating solution to produce a compound having an aldehyde group. As a result, an electrophotographic photosensitive member produced using a coating solution that has undergone decomposition has been disadvantageous in that the residual potential increases due to the influence of aldehyde, and thus it has been difficult to use. As for the coating solution for producing an electrophotographic photosensitive member, it is common to use a once-prepared solution many times in a span of several months, and this defect is fatal. In particular, this decomposition is remarkable when the polyarylate resin is included in the coating solution, and it is particularly difficult to use it in combination with polyarylate. Therefore, a method for stably using an enamine compound has been strongly desired so far.

  Further, it has been reported that in a contact charging method, in particular, a contact charging method image forming apparatus in which an alternating voltage is superimposed, surface deterioration tends to proceed because discharge occurs in the vicinity of the surface of the photoreceptor (Non-Patent Document 1). The enamine that has undergone the above-described decomposition has a low resistance and is particularly disadvantageous in the contact charging method.

  In addition, it has been reported that it is effective to use a polyarylate resin as a binder resin in response to the recent demand for high printing durability photoreceptors (Patent Document 4). However, when the polyarylate resin is used, there is a problem that the charge transport material is decomposed in the coating liquid and the deterioration of the liquid tends to proceed as compared with the conventionally used polycarbonate resin. The enamine compound mentioned above is the case, but deterioration is also observed in other charge transport materials. In charge transport materials other than enamines, decomposition with a compound having a conjugated double bond is likely to proceed, and examples thereof include butadiene compounds. The cause of this decomposition has not been elucidated at present, but it is considered that one of the causes is a terminal carboxylic acid group remaining in the polyarylate resin.

JP-A-1-195455 JP-A-6-332205 JP-A-6-348046 Japan Hardcopy 2001 Fall Meeting (32-35) JP 2006-53549 A

  An object of the present invention is to provide a coating solution that can suppress deterioration over time even when the coating solution contains a polyarylate resin. Also, an electrophotographic photoreceptor having excellent photosensitivity, residual potential, charge mobility, gas resistance, and abrasion resistance, formed using the coating solution, and an image forming apparatus provided with the photoreceptor, and It is an object to provide an electrophotographic photosensitive member cartridge.

As a result of diligent studies to improve the above problems, the present inventors suppressed the deterioration of the coating liquid by containing a non-nitrogen acid scavenger in the coating liquid, and were prepared using this coating liquid. The electrophotographic photoreceptor exhibits excellent electrical characteristics, specifically, photosensitivity, residual potential, charge mobility, gas resistance, and abrasion resistance, and can provide a stable image even after repeated use. Clarified and completed the following invention.
A first aspect of the present invention is a coating solution for producing an electrophotographic photosensitive member containing a charge transporting material, which contains a non-nitrogen acid scavenger. is there.

In the first aspect of the present invention, the non-nitrogen acid scavenger is preferably an epoxy group-containing compound.
The coating solution for producing an electrophotographic photosensitive member of the first invention preferably contains a polyarylate resin. The polyarylate resin preferably has a repeating structure represented by the following formula (A).

（式（Ａ）中、Ａｒ^ａ１〜Ａｒ^ａ４はそれぞれ独立に置換基を有してもよいアリーレン基を表し、Ｘ、Ｙは単結合又は二価基を表し、ｋは０または１を表す。）

(In the formula (A), Ar ^{a1 to} Ar ^a4 each independently represent an arylene group which may have a substituent, X and Y each represents a single bond or a divalent group, and k represents 0 or 1 . )

In the first aspect of the present invention, the charge transport material, Ru der enamine compound.

  According to a second aspect of the present invention, there is provided an electrophotographic photosensitive member having a photosensitive layer on a conductive support, wherein the photosensitive layer contains a charge transport material and a non-nitrogen acid scavenger. It is.

  In the second aspect of the present invention, the non-nitrogen acid scavenger is preferably an epoxy group-containing compound.

  In the second invention, the photosensitive layer preferably contains a polyarylate resin. The polyarylate resin preferably has a repeating structure represented by the following formula (A).

（式（Ａ）中、Ａｒ^ａ１〜Ａｒ^ａ４はそれぞれ独立に置換基を有してもよいアリーレン基を表し、Ｘ、Ｙは単結合又は二価基を表し、ｋは０または１を表す。）

(In the formula (A), Ar ^{a1 to} Ar ^a4 each independently represent an arylene group which may have a substituent, X and Y each represents a single bond or a divalent group, and k represents 0 or 1 . )

In the second aspect of the present invention, the charge transport material, Ru der enamine compound.

  According to a third aspect of the present invention, there is provided an electrophotographic photosensitive member according to the second aspect of the invention, a charging means for charging the electrophotographic photosensitive member, and an image that forms an electrostatic latent image by performing image exposure on the charged electrophotographic photosensitive member. An image forming apparatus comprising: an exposure unit; a developing unit that develops the electrostatic latent image with toner; and a transfer unit that transfers the toner to a transfer target.

  In the third aspect of the present invention, the charging means is preferably a contact charging system.

  According to a fourth aspect of the present invention, there is provided charging means for charging the electrophotographic photosensitive member, image exposure means for performing image exposure on the charged electrophotographic photosensitive member to form an electrostatic latent image, and developing the electrostatic latent image with toner. An electrophotographic photosensitive member cartridge comprising: at least one means selected from the group consisting of developing means for transferring, and transferring means for transferring the toner to a transfer target; and the electrophotographic photosensitive member of the second invention. It is.

  In the fourth invention, the charging means is preferably a contact charging system.

  By including a non-nitrogen acid scavenger in the coating solution for producing an electrophotographic photoreceptor, decomposition of the charge transport material in the coating solution is suppressed. An electrophotographic photoreceptor containing a non-nitrogen acid scavenger in the photosensitive layer exhibits excellent photosensitivity, residual potential, charge mobility, and gas resistance.

  Hereinafter, embodiments of the present invention will be described in detail. However, the description of the constituent elements described below is a representative example of the embodiments of the present invention, and is appropriately modified and implemented without departing from the spirit of the present invention. can do.

<Electrophotographic photoreceptor>
The electrophotographic photoreceptor of the present invention is characterized in that the photosensitive layer contains at least a non-nitrogen acid scavenger. In the case where the photosensitive layer of the electrophotographic photosensitive member is a laminate type described later, the charge transporting layer includes a non-nitrogen acid scavenger, a binder resin, a charge transporting material, and, if necessary, an antioxidant, a leveling agent, Other additives are included. In addition, when the electrophotographic photosensitive layer is a single-layer type, which will be described later, in addition to the components used for the charge transport layer of the photoconductor, a charge generating material and an electron transport material may be used. It is common.

<Non-nitrogen acid scavenger>
In the present invention, the non-nitrogen acid scavenger indicates a compound that does not have a nitrogen atom in the molecule and chemically changes by chemically reacting with an acid, or a compound that reduces acidity by an equilibrium reaction. As an acid scavenger having a nitrogen atom in the molecule, there is an alkylamine, but if it is present in an electrophotographic photoreceptor, the residual potential increases, which is not preferable.
Examples of the acid scavenger that can be used in the present invention include an epoxy group-containing compound and a non-nitrogen weak base.

As an epoxy group containing compound, if an epoxy group is contained in a molecule | numerator, there will be no restriction | limiting in the structure. The number of epoxy groups in the molecule is usually 10 or less, preferably 2 or less, more preferably 1. This is because when a plurality of epoxy groups are contained in the molecule, there is a possibility of causing a crosslinking reaction with the binder resin and causing the coating solution to change in viscosity.
The molecule may have a functional group other than an epoxy group, but preferably an aromatic hydrocarbon and an aliphatic hydrocarbon and an epoxy group are preferable, and only an aliphatic hydrocarbon and an epoxy group are included. Is more preferable.

The molecular weight of the epoxy group-containing compound is usually 100 or more, preferably 150 or more, more preferably 200 or more, because a very small molecular weight tends to have mutagenic properties. On the other hand, if it is too large, the viscosity may change in the coating solution. Therefore, it is usually 2,000 or less, preferably 1,000 or less, more preferably 500 or less.
Specific examples of the epoxy group-containing compound are illustrated below.

  When the content of these epoxy group-containing compounds in the coating solution is too small, the effect of suppressing the decomposition of the charge transport material in the coating solution cannot be obtained sufficiently, and when it is too large, when used in an electrophotographic photoreceptor. Residual potential increases when used repeatedly. An epoxy group containing compound is 0.01 mass% or more normally with respect to the binder total mass, Preferably it is 0.1 mass% or more, More preferably, it is 0.3 mass% or more. Moreover, an epoxy group containing compound is 10 mass% or less normally, Preferably it is 5 mass% or less, More preferably, it is 1 mass% or less.

Examples of the non-nitrogen weak base include sodium acetate, sodium benzoate, disodium terephthalate, disodium isophthalate, and disodium diphenyl ether-4,4′-dicarboxylate.
The non-nitrogen acid scavenger is preferably an organic acid scavenger that does not contain an inorganic substance, and most preferably an epoxy group-containing compound, from the viewpoint of residual potential.

<Enamine compound>
The enamine compound that can be used in the present invention may be any enamine compound having a partial structure represented by the following formula (1) in the molecule.

（式（１）中、Ｒ^１、Ｒ^２、Ｒ^３、Ｒ^４、Ｒ^５はそれぞれ独立して水素原子、又は置換基を表す）

(In formula (1), R ¹ , R ² , R ³ , R ⁴ , R ⁵ each independently represents a hydrogen atom or a substituent)

  The number of enamine structures in the molecule of the enamine compound is arbitrary, but is usually 1 or more, and preferably 2 or more from the viewpoint of the characteristics of the electrophotographic photoreceptor. In addition, the enamine structure part has low durability against acidity, and if there are many enamine structure parts in the molecule, it can be decomposed by a gas such as ozone when used as an electrophotographic photoreceptor, and affect the characteristics of the electrophotographic photoreceptor. Therefore, it is preferably 5 or less, more preferably 4 or less, still more preferably 3 or less, and particularly preferably 2 or less.

R ¹ , R ² , R ³ , R ⁴ and R ⁵ each independently represent a hydrogen atom or a substituent, but usually R ¹ , R ⁴ and R ⁵ are substituents, and the stability of the enamine compound In view of the above, it is preferable that R ¹ , R ² , R ⁴ and R ⁵ are substituents.

The structure suitable as an enamine compound is demonstrated below.
In the case of a compound having one enamine structure in the molecule, the structure of the following formula (2) is preferable.

（式（２）中、Ａｒ^１、Ａｒ^２、Ａｒ^３はそれぞれ独立して置換基を有していてもよいアリール基を表し、Ｒ^２、Ｒ^３はそれぞれ独立して水素原子、又は置換基を表す。）

(In the formula (2), Ar ¹ , Ar ² and Ar ³ each independently represent an aryl group which may have a substituent, and R ² and R ³ each independently represent a hydrogen atom or a substituent. Represents.)

In formula (2), Ar ¹ , Ar ² , and Ar ³ each independently represent an aryl group that may have a substituent. Examples of the aryl group include a phenyl group, a naphthyl group, an anthryl group, a phenanthryl group, and a fluorenyl group. Among these, in consideration of the characteristics of the electrophotographic photoreceptor, a phenyl group, a naphthyl group, and a fluorenyl group are preferable, a phenyl group and a naphthyl group are more preferable, and a phenyl group is still more preferable. Ar ² and Ar ³ can also form a cyclic structure via a direct bond or a linking group. Specific examples of the linking group include a carbonyl group (representing divalent —C (═O) —), a sulfinyl group, a sulfonyl group, a sulfinato group, an alkylene group, an alkenylene group, an alkylidene group, an oxy group, a seleno group, Examples thereof include a thio group, and an alkylene group and an alkenylene group are preferable. One linking group may be used alone, or two or more linking groups may be used in any ratio and combination.

Ar ¹ , Ar ² and Ar ³ may further have a substituent, and examples of the substituent include an alkyl group which may have a substituent and an aryl group which may have a substituent. , An alkoxy group which may have a substituent, an aralkyloxy group which may have a substituent, an aryloxy group which may have a substituent, the following structural formula (3), the following structural formula ( 4) and the like. Among these substituents, from the viewpoint of characteristics as an electrophotographic photoreceptor, an alkyl group which may have a substituent, an alkoxy group which may have a substituent, the following structural formula ( 3) The following structural formula (4) is preferable, and from the viewpoint of charge transport mobility, an alkyl group having 3 or less carbon atoms which may have a substituent, or 3 or less carbon atoms which may have a substituent. And the following structural formula (4) is preferable: Further methyl group, an ethyl group, a methoxy group, the following structural formula (3), the following structural formula (4) are preferred, even more preferably, a methyl group, the following structural formula (3), a following structural formula (4).

（式（３）中、Ｒ^６、Ｒ^７、Ｒ^８、Ａｒ^４、Ａｒ^５はそれぞれ独立して水素原子、置換基を有していてもよいアルキル基、置換基を有していてもよいアリール基を表し、Ａｒ^４、Ａｒ^５のうち少なくとも一つは置換基を有していてもよいアリール基である。ｎは０ないし２の整数を表す。）

(In Formula (3), R ⁶ , R ⁷ , R ⁸ , Ar ⁴ , Ar ⁵ may each independently have a hydrogen atom, an alkyl group which may have a substituent, or a substituent. Represents an aryl group, and at least one of Ar ⁴ and Ar ^{5 is} an aryl group which may have a substituent, and n represents an integer of 0 to 2.

In formula (3), R ⁶ , R ⁷ and R ⁸ each independently represent a hydrogen atom, an alkyl group which may have a substituent, or an aryl group which may have a substituent. , A hydrogen atom, and an optionally substituted alkyl group are preferred, and a hydrogen atom is more preferred from the viewpoint of charge transport ability. Among these, it is more preferable that all of R ⁶ , R ⁷ and R ⁸ are hydrogen atoms. Ar ⁴ and Ar ⁵ each independently represent a hydrogen atom, an alkyl group which may have a substituent, or an aryl group which may have a substituent, and at least one of Ar ⁴ and Ar ⁵ is substituted. An aryl group which may have a group.

Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, an isopropyl group, a tertiary butyl group, and a cyclohexylmethyl group. Among these, an alkyl group having 3 or less carbon atoms is preferable from the viewpoint of charge transport ability. More preferably, it is a methyl group. Examples of the aryl group include a phenyl group, a naphthyl group, an anthryl group, a phenanthryl group, and a fluorenyl group. Among these, in consideration of the characteristics of the electrophotographic photoreceptor, a phenyl group, a naphthyl group, and a fluorenyl group are preferable, a phenyl group and a naphthyl group are more preferable, and a phenyl group is still more preferable. In the case where Ar ⁴ is an aryl group which may have a substituent, Ar ⁵ is an aryl group which may have a substituent or a hydrogen atom in terms of residual potential of the electrophotographic photosensitive member. Is preferred. Among these combinations, it is more preferable that Ar ⁴ is a phenyl group which may have a substituent, Ar ⁵ is a phenyl group which may have a substituent, or a hydrogen atom. n represents an integer of 0 to 2. Since n may increase the solubility when n increases, n is preferably 0 to 1. Ar ⁴ and Ar ⁵ can also form a cyclic structure via a direct bond or a linking group.

（式（４）中、Ｒ^９、Ｒ^１０、Ｒ^１１、Ａｒ^６、Ａｒ^７はそれぞれ独立して水素原子、置換基を有していてもよいアルキル基、置換基を有していてもよいアリール基を表し、Ａｒ^６、Ａｒ^７のうち少なくとも一つは置換基を有していてもよいアリール基である。ｍは０ないし２の整数を表す。）

(In Formula (4), R ⁹ , R ¹⁰ , R ¹¹ , Ar ⁶ , Ar ⁷ may each independently have a hydrogen atom, an alkyl group that may have a substituent, or a substituent. Represents an aryl group, and at least one of Ar ⁶ and Ar ^{7 is} an aryl group which may have a substituent, and m represents an integer of 0 to 2.

In formula (4), R ⁹ , R ¹⁰ and R ¹¹ each independently represent a hydrogen atom, an alkyl group which may have a substituent, or an aryl group which may have a substituent. , A hydrogen atom, and an optionally substituted alkyl group are preferred, and a hydrogen atom is more preferred from the viewpoint of charge transport ability. Among these, it is more preferable that all of R ⁹ , R ¹⁰ and R ¹¹ are hydrogen atoms. Ar ⁶ and Ar ⁷ each independently represent a hydrogen atom, an alkyl group which may have a substituent, or an aryl group which may have a substituent, and at least one of Ar ⁶ and Ar ⁷ is substituted. Even if it has a group, it is an aryl group.

  Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, an isopropyl group, a tertiary butyl group, and a cyclohexylmethyl group. Among these, an alkyl group having 3 or less carbon atoms is preferable from the viewpoint of charge transport ability. More preferably, it is a methyl group. Examples of the aryl group include a phenyl group, a naphthyl group, an anthryl group, a phenanthryl group, and a fluorenyl group. Among these, in consideration of the characteristics of the electrophotographic photoreceptor, a phenyl group, a naphthyl group, and a fluorenyl group are preferable, a phenyl group and a naphthyl group are more preferable, and a phenyl group is still more preferable.

When Ar ⁶ is an aryl group which may have a substituent, Ar ⁷ has an aryl group which may have a substituent or a substituent from the viewpoint of the repeating characteristics of the electrophotographic photosensitive member. It is preferably an alkyl group that may be present. Among these combinations, it is more preferable that Ar ⁶ is a phenyl group which may have a substituent, and Ar ⁷ is a phenyl group which may have a substituent. m represents an integer of 0 to 2. Since m may increase the solubility when m increases, m is preferably 0 to 1. Ar ⁶ and Ar ⁷ can also form a cyclic structure via a direct bond or a linking group.

In formula (2), R ² and R ³ each independently represent a hydrogen atom or a substituent. The type of the substituent is not limited, and when R ² and R ³ are substituents, for example, an alkyl group which may have a substituent, an aryl group which may have a substituent, and a substituent. Examples thereof include an alkoxy group which may have, an aralkyloxy group which may have a substituent, and an aryloxy group which may have a substituent. Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, an isopropyl group, a tertiary butyl group, and a cyclohexylmethyl group. Examples of the aryl group include a phenyl group, a naphthyl group, an anthryl group, a phenanthryl group, and a fluorenyl group. Examples of the alkoxy group include a methoxy group, an ethoxy group, and a propoxy group. Examples of the aralkyloxy group include a benzyloxy group. Examples of the aryloxy group include phenoxy group and 1-naphthoxy group. Among these, an alkyl group which may have a substituent and an aryl group which may have a substituent are preferable, and an alkyl group having 3 or less carbon atoms and a carbon number of 10 from the viewpoint of the characteristics of the electrophotographic photoreceptor. The following aryl groups are more preferable, more preferably a methyl group, an ethyl group, an optionally substituted phenyl group or a naphthyl group, and even more preferably a methyl group or a substituent. It is a phenyl group.

R ² is preferably an aryl group which may have a substituent since the stability of the enamine compound is improved as the molecular structure is moderately bulky. Among them, a phenyl group and a naphthyl group are preferable, and a phenyl group is more preferable. It is a group. R ^{3 has a} bulky substituent, which affects the charge transport ability. Therefore, an alkyl group and a hydrogen atom which may have a substituent are preferable, and a hydrogen atom is more preferable.

R ² and R ³ can also form a cyclic structure via R ² and R ³ , or directly bonded to Ar ¹ , Ar ² and Ar ³ , or via a linking group. Specific examples of the linking group include a carbonyl group (representing divalent —C (═O) —), a sulfinyl group, a sulfonyl group, a sulfinato group, an alkylene group, an alkenylene group, an alkylidene group, an oxy group, a seleno group, Examples include a thio group, and a carbonyl group, an alkylene group, and an alkenylene group are preferable. One linking group may be used alone, or two or more linking groups may be used in any ratio and combination.

  In the case of a compound having two enamine structures in the molecule, the structure of the following formula (5) is preferable.

In the formula (5), Ar ⁸ , Ar ⁹ , Ar ¹⁰ , Ar ¹¹ , Ar ¹² and Ar ¹³ are the same as Ar ¹ and Ar ² in the formula (2). R ¹² , R ¹³ , R ¹⁴ and R ¹⁵ are the same as R ² and R ³ in the formula (2).

  In the above formula (5), X represents a direct bond or a linking group that connects two enamine structure moieties having a molecular weight of 14 or more and 400 or less. If the molecular weight is too large, there is a possibility of crystal precipitation in the coating solution. Therefore, it is preferably 350 or less, more preferably 300 or less.

When X represents a direct bond, it is possible to form a direct bond at any part between the enamine structure parts. The two enamine structural moieties are usually bonded to any of Ar ⁸ , Ar ⁹ , Ar ¹⁰ and any of Ar ¹¹ , Ar ¹² , Ar ¹³ , or a direct bond between R ¹² and R ¹⁴ moieties. Form. Among these combinations of sites that directly bond, from the viewpoint of the characteristics of the electrophotographic photosensitive member, any of Ar ⁹ and Ar ¹⁰ and any of Ar ¹² and Ar ¹³ are directly bonded, or R ¹² and R ^{12 14} is preferably directly bonded, and more preferably any of Ar ⁹ and Ar ¹⁰ and any of Ar ¹² and Ar ¹³ are directly bonded.

  A preferred structure when X is a direct bond is shown in the following formula (6).

In the formula (6), Ar ⁸ , Ar ⁹ , Ar ¹⁰ , Ar ¹¹ , Ar ¹² and Ar ¹³ are the same as Ar ¹ and Ar ² in the formula (2). R ¹² , R ¹³ , R ¹⁴ and R ¹⁵ are the same as R ² and R ³ in the formula (2).

When X represents a linking group, the linking group X usually has a molecular weight of 14 or more and 400 or less. When the linking group X is substituted with a substituent described later, the entire molecular weight including the molecular weight of the substituent preferably satisfies the above range.
Specific examples of the linking group X include a group having a heterocyclic ring which may have a substituent and a ring having aromaticity which may have a substituent (hereinafter referred to as “aromatic ring” as appropriate). group having the group having a good condensed polycyclic ring which may have a substituent, a group having an optionally substituted aliphatic hydrocarbon _{group, -O- (CH 2) n -O-} , Etc. In addition, the coupling group X may be used individually by 1 type, and may be used 2 or more types by arbitrary ratios and combinations.

When the linking group X is a group having an aromatic ring which may have a substituent, the aromatic ring is preferably an arylene group, and among the arylene groups, a phenylene group, a naphthylene group, an anthrylene group, and a phenanthrylene group are preferable. . Among these, a phenylene group and a naphthylene group are more preferable, and a phenylene group is still more preferable.
When the linking group X is a group having a condensed polycycle which may have a substituent, the condensed polycycle is preferably tetralin, azulene or fluorene, more preferably tetralin or fluorene, and further preferably fluorene.

When the linking group X is a group having an aliphatic hydrocarbon group which may have a substituent, the aliphatic hydrocarbon group is preferably an alkylene group, an alkenylene group, an alkynylene group or an alkylidene group.
When the linking group X is an alkylene group, an alkylene group having 1 or more, preferably 2 or more, and usually 20 or less, preferably 15 or less, more preferably 10 or less is desirable.
When the linking group X is an alkenylene group, an alkenylene group having 2 or more carbon atoms and usually 20 or less, preferably 15 or less, more preferably 10 or less is desirable.
When the linking group X is an alkynylene group, an alkynylene group having 2 or more carbon atoms, usually 20 or less, preferably 15 or less, more preferably 10 or less is desirable.
When the linking group X is an alkylidene group, an alkylidene group whose carbon number is usually 2 or more, preferably 3 or more, and usually 9 or less, preferably 6 or less is desirable.
Moreover, the aliphatic hydrocarbon group which may have a substituent may be linear or branched. Further, it may be a chain or a ring. Furthermore, it may have only a saturated bond or may have an unsaturated bond.

  When the linking group X is a group having a heterocyclic ring, examples of the linking group X include those having one or more elements selected from the group consisting of nitrogen, oxygen, and sulfur. Is, for example, a heteroaryl such as a divalent group having an indole ring, a divalent group having an oxazole ring, a divalent group having an isoxazole ring, a divalent group having an oxadiazole ring, or a divalent group having a thiophene ring. Examples thereof include a divalent group having a ring.

  The linking group X may have a substituent. The number of substituents may be one, or two or more substituents may be used in any ratio and combination. The type of the substituent is not limited. For example, the alkyl group which may have a substituent, the aryl group which may have a substituent, the alkoxy group which may have a substituent, a halogen atom, Examples thereof include a cyano group and a nitro group. Among these, an alkyl group which may have a substituent, an aryl group which may have a substituent, and an alkoxy group which may have a substituent A halogen atom is preferred.

  Among the above linking groups, when comprehensively considering the production efficiency of the enamine compound, the stability of the coating solution, the charge transport ability, and the properties as an electrophotographic photosensitive member, an arylene group and a saturated hydrocarbon group are more preferable, an arylene group, More preferred are an alkylidene group and an alkenylene group.

  A preferred structure when X is a linking group is shown in the following formula (7).

式（７）中、Ａｒ^８、Ａｒ^９、Ａｒ^１０、Ａｒ^１１、Ａｒ^１２、Ａｒ^１３は、式（２）中のＡｒ^１、Ａｒ^２と同様である。また、Ｒ^１２、Ｒ^１３、Ｒ^１４、Ｒ^１５に関しては、式（２）中のＲ^２とＲ^３と同様である。Ｙは酸素原子、又は下記式（８）、（９）、（１０）で表される。

In the formula (7), Ar ⁸ , Ar ⁹ , Ar ¹⁰ , Ar ¹¹ , Ar ¹² , Ar ¹³ are the same as Ar ¹ and Ar ² in the formula (2). R ¹² , R ¹³ , R ¹⁴ and R ¹⁵ are the same as R ² and R ³ in the formula (2). Y is represented by an oxygen atom or the following formulas (8), (9), and (10).

（式（８）中、Ｒ^１６、Ｒ^１７、Ｒ^１８、Ｒ^１９は、それぞれ独立して水素原子、置換基を有していてもよいアルキル基、置換基を有してもよいアリール基を表し、Ａｒ^１４は置換基を有していてもよいアリーレン基を表す。ｋ１は１以上３以下の整数を表す。）

(In the formula (8), R ¹⁶ , R ¹⁷ , R ¹⁸ and R ¹⁹ are each independently a hydrogen atom, an alkyl group which may have a substituent, or an aryl group which may have a substituent. Ar ¹⁴ represents an arylene group which may have a substituent, and k1 represents an integer of 1 to 3.

（式（９）中、Ｒ^２０、Ｒ^２１は、それぞれ独立して水素原子、置換基を有していてもよいアルキル基、置換基を有していてもよいアリール基を表す。）

(In Formula (9), R ²⁰ and R ²¹ each independently represent a hydrogen atom, an alkyl group which may have a substituent, or an aryl group which may have a substituent.)

（式（１０）中、Ａｒ^１５は置換基を有していてもよいアリーレン基を表す。ｌは１以上３以下の整数を表す。）

(In the formula (10), Ar ¹⁵ represents an arylene group which may have a substituent. L represents an integer of 1 or more and 3 or less.)

In the above formula (8), R ¹⁶ , R ¹⁷ , R ¹⁸ and R ¹⁹ are each independently a hydrogen atom, an alkyl group which may have a substituent, or an aryl group which may have a substituent. Among these, a hydrogen atom and an alkyl group which may have a substituent are preferable, and a hydrogen atom is more preferable from the viewpoint of charge transport ability. Among these, it is more preferable that all of R ¹⁶ , R ¹⁷ , R ¹⁸ and R ¹⁹ are hydrogen atoms. Ar ¹⁴ represents an arylene group which may have a substituent. Examples of the arylene group include a phenylene group, a naphthylene group, an anthrylene group, and a phenanthrylene group. Among these, a phenylene group and a naphthylene group are preferable, and a phenylene group is more preferable in consideration of the characteristics of the electrophotographic photoreceptor. k1 represents an integer of 1 to 3. Since the increase in the number of k1 may lead to a decrease in the solubility of the enamine compound, it is preferably 2 or less, more preferably 1.

In the above formula (9), R ²⁰ and R ²¹ each independently represent a hydrogen atom, an alkyl group which may have a substituent, or an aryl group which may have a substituent. Examples of the alkyl group which may have a substituent include a methyl group, an ethyl group, a propyl group, an isopropyl group, a tertiary butyl group, and a cyclohexylmethyl group. Examples of the aryl group include a phenyl group, a naphthyl group, an anthryl group, a phenanthryl group, and a fluorenyl group. Among these substituents, in consideration of the characteristics of the electrophotographic photoreceptor, an alkyl group having 10 or less carbon atoms and an aryl group having 10 or less carbon atoms are preferable, an alkyl group having 6 or less carbon atoms, and an aryl group having 6 or less carbon atoms. Is more preferable. R ²⁰ and R ²¹ can also form a cyclic structure via a direct bond or a linking group.

In the formula (10), Ar ¹⁵ represents an arylene group which may have a substituent. Examples of the arylene group include a phenylene group, a biphenylene group, a naphthylene group, an anthrylene group, and a phenanthrylene group. Among these, a phenylene group and a naphthylene group are preferable, and a phenylene group is more preferable in consideration of the characteristics of the electrophotographic photoreceptor. It is. l represents an integer of 1 or more and 3 or less. Since the increase in the number of l may lead to a decrease in the solubility of the enamine compound, it is preferably 2 or less, more preferably 1.

  The structure of an enamine compound suitable for the present invention is exemplified below. The following structures are illustrated to make the present invention more concrete, and are not limited to the following structures without departing from the concept of the present invention.

（Ｒは同一でも、それぞれ異なっていてもかまわない。具体的には、水素原子又は、置換基；置換基としては、アルキル基、アルコキシ基、アリール基等が好ましい。中でも、特に好ましくは、メチル基、エチル基、メトキシ基、フェニル基である。また、ｎは０ないし２の整数である。）

(R may be the same or different from each other. Specifically, a hydrogen atom or a substituent; as a substituent, an alkyl group, an alkoxy group, an aryl group, etc. are preferable. Group, ethyl group, methoxy group, and phenyl group, and n is an integer of 0 to 2.)

<Butadiene compound>
The butadiene compound used in the present invention indicates all compounds having a butadiene skeleton in the molecule. Among these, a compound represented by the following formula (11) is preferable.

In formula (11), Ar ³¹ to Ar ³⁶ each independently represents an aromatic group which may have a substituent, and X ³¹ to X ³² each independently represent the following formula (12). .

In formula (12), R ³¹ to R ³⁵ each independently represent a hydrogen atom, or an alkyl group or aryl group which may have a substituent. n1 to n2 represent an integer of 0 or 1, and n3 represents an integer of 1 to 3.
Ar ³¹ to Ar ³⁶ in the formula (11) each independently represents an aromatic group which may have a substituent. As the aromatic group, any group having aromaticity may be used, and examples thereof include an aromatic hydrocarbon group and an aromatic heterocyclic group. Examples of the aromatic hydrocarbon group include a phenyl group, a naphthyl group, an anthryl group, and a pyrenyl group. Examples of the aromatic heterocyclic group include a thiophenyl group and a pyrrolyl group. Preferred is an aromatic hydrocarbon group, and preferred is a group having 4 or less rings, and particularly preferred is a phenyl group.

These substituents that the aromatic group may have include methyl group, ethyl group, propyl group, isopropyl group, pentyl group, isopentyl group, neopentyl group, 1-methylbutyl group, 1-methylheptyl group, dodecyl group. Group, hexadecyl group, alkyl group such as octadecyl group; aryl group such as phenyl group, naphthyl group, anthryl group, pyrenyl group; aralkyl group such as benzyl group, phenethyl group; alkoxy group such as methoxy group, ethoxy group; hydroxy group A nitro group; a halogen atom. As a preferred substituent, an alkyl group, an alkoxy group or an aryl group having 10 or less carbon atoms is preferable, and an alkyl group or an alkoxy group having 4 or less carbon atoms is more preferable. Groups are preferred. These substituents may be present independently in Ar ³¹ to Ar ³⁶ .

  The substituent that the aromatic group may have may further have a substituent, such as an alkyl group, an alkoxy group, or an aryl group having 10 or less carbon atoms as described above. More preferably, it is an alkyl group or an alkoxy group having 4 or less carbon atoms.

Ar ³¹ to Ar ³⁶ may form a condensed ring through the aforementioned substituent or linking group, or may be directly connected to form a condensed ring. The linking group is a divalent residue having 20 or less carbon atoms.

Of Ar ³¹ to Ar ³⁶ in formula (11), Ar ³³ and Ar ³⁴ preferably have an alkoxy group or an alkyl group as a substituent. Ar ³³ and Ar ³⁴ are preferably aryl groups. In this case, it is preferable that an alkoxy group or an alkyl group is present at the 2-position or the 4-position with respect to the nitrogen atom. As the alkyl group substituted for Ar ³³ and Ar ³⁴ , an alkyl group having 4 or less carbon atoms is preferable, and a methyl group is particularly preferable. As the alkoxy group substituted for Ar ³³ and Ar ³⁴ , an alkoxy group having 4 or less carbon atoms is preferable, and a methoxy group is particularly preferable. In addition, Ar ³³ and Ar ³⁴ are preferably the same from the viewpoint of ease of synthesis.

X ³¹ to X ³² are each independently a group represented by the formula (12). In formula (12), R ³¹ to R ³⁵ are a hydrogen atom, or an alkyl group or aryl group which may have a substituent. X ¹ and X ² may be the same or different from each other. Examples of the aryl group include a phenyl group, a naphthyl group, an anthryl group, a pyrenyl group, a biphenylyl group, a terphenylyl group, and the like, preferably those having 3 or less aromatic rings, and particularly preferably a phenyl group. Examples of the alkyl group include alkyl groups such as a methyl group, an ethyl group, a propyl group, an isopropyl group, a pentyl group, an isopentyl group, a neopentyl group, a 1-methylbutyl group, a 1-methylheptyl group, a dodecyl group, a hexadecyl group, and an octadecyl group. However, an alkyl group having 8 or less carbon atoms is preferable, and an alkyl group having 4 or less carbon atoms is more preferable.

When R ³¹ to R ³⁵ are an alkyl group or an aryl group which may have a substituent, the substituent is preferably a substituent having 10 or less carbon atoms, specifically, a methyl group, Alkyl groups such as ethyl group, propyl group, isopropyl group, pentyl group, isopentyl group, neopentyl group, 1-methylbutyl group, 1-methylheptyl group, dodecyl group, hexadecyl group, octadecyl group; phenyl group, naphthyl group, anthryl group And aryl groups such as pyrenyl group; aralkyl groups such as benzyl group and phenethyl group; alkoxy groups such as methoxy group and ethoxy group; hydroxy group; nitro group; halogen atoms. You may have. R ³¹ to R ³⁵ may form a condensed ring via the aforementioned substituent or linking group, or may be directly connected to form a condensed ring.

  Moreover, n1 thru | or n2 in Formula (11) represent the integer of 0 or 1, and n3 in Formula (12) represents 1 thru | or 3. n3 is preferably not too large in view of electrical characteristics, and is preferably 2 or less. More preferably, it is 1. When considering the overall performance, n2 is preferably 1, and n1 is preferably 1.

Moreover, it is preferable that the compound represented by Formula (11) is a composition in which geometric isomers are mixed. When n2 is 1, the geometric isomerism of the double bond closest to Ar ³¹ to Ar ³² in X ³¹ and X ³² represented by the formula (12) is preferably a cis-trans mixture. Specifically, among X ¹ and X ² represented by the formula (12), 30% or more is preferably a cis isomer, and 40% or more is more preferably a cis isomer. In addition, when n2 is 0, 80% or more of X ¹ and X ² represented by the formula (12) is preferably a trans isomer, more preferably 85% or more is a trans isomer, More preferably, 90% or more is a trans isomer.

  Next, specific examples of the structure of the compound represented by the formula (11) are illustrated below. The following exemplary compounds are exemplified for the purpose of explaining the present invention in detail, and the compound represented by the formula (11) is not limited to the following structure unless it is contrary to the gist of the present invention. .

<Coating solution>
The coating solution of the present invention is used for forming a photosensitive layer of an electrophotographic photoreceptor, and is at least a solution or dispersion containing a charge transport material and a non-nitrogen acid scavenger.
The coating liquid of the present invention is mainly used as a coating liquid for forming a charge transport layer when the photosensitive layer of the electrophotographic photosensitive member is a laminated type photosensitive member to be described later, and includes a non-nitrogen acid scavenger and a binder resin. , A charge transport material, a solvent, and the like, if necessary, an antioxidant, a leveling agent, and other additives. In the case where the electrophotographic photosensitive layer is a single layer type, which will be described later, it is common to use a charge generating material and an electron transporting material in addition to the components of the charge transport layer forming coating solution. By applying these, an electrophotographic photoreceptor can be produced.

  The coating liquid of the present invention can be prepared by simply mixing a non-nitrogen acid scavenger and various materials necessary for the photosensitive layer of the electrophotographic photoreceptor described later. Although the order of mixing the materials is not particularly specified, it is preferable to add the charge transport material after dissolving the non-nitrogen acid scavenger and the binder resin. At the time of producing the binder resin, a non-nitrogen acid scavenger may be added to prepare a composition of the binder resin and the non-nitrogen acid scavenger in advance. It is also possible to heat the material after mixing. The temperature for heating the solvent is 40 ° C. or higher when the container is opened to atmospheric pressure, and is 10 ° C. or lower than the boiling point of the lowest boiling compound among the compounds contained in the solvent. Can be heated in a range. The coating solution may be produced with the container sealed. In this case, all the raw materials constituting the coating solution are put in a sealable container, and while stirring and mixing, the internal temperature is heated to 30 ° C. to 100 ° C. and maintained for 1 hour to 10 hours to produce the coating solution. Can do. However, considering the liquid stability of the coating solution, it is preferable to dissolve at 40 ° C. or lower, preferably 30 ° C. or lower, more preferably 20 ° C. or lower.

  There are no particular restrictions on the solvent or dispersion medium used for the preparation of the coating solution, but specific examples include alcohols such as methanol, ethanol, propanol and 2-methoxyethanol, tetrahydrofuran, 1,4-dioxane, dimethoxyethane and the like. Ethers, esters such as methyl formate and ethyl acetate, acetone, methyl ethyl ketone, cyclohexanone, ketones such as 4-methoxy-4-methyl-2-pentanone, aromatic hydrocarbons such as benzene, toluene, xylene, dichloromethane, Chlorinated hydrocarbons such as chloroform, 1,2-dichloroethane, 1,1,2-trichloroethane, 1,1,1-trichloroethane, tetrachloroethane, 1,2-dichloropropane, trichloroethylene, n-butylamine, isopropanolamine, Diethyla Emissions, triethanolamine, ethylenediamine, nitrogen-containing compounds such as triethylenediamine, acetonitrile, N- methylpyrrolidone, N, N- dimethylformamide, aprotic polar solvents such as dimethyl sulfoxide and the like. Moreover, these may be used individually by 1 type and may use 2 or more types together by arbitrary combinations and kinds.

  The coating solution normally absorbs water in the atmosphere and contains water, but in the present invention, it is preferable to control the amount of water in the solvent within a certain range. This is because the smaller the water content, the more the generation of aldehyde due to the hydrolysis of enamine can be suppressed, and the increase in the residual potential in the photoreceptor can be suppressed. The amount of water in the coating solution is usually 1% by mass or less, preferably 0.5% by mass or less, more preferably 0.3% by mass or less, and most preferably 0.1% by mass or less. The amount of water in the coating solution can be measured using a Karl Fischer moisture meter.

  The storage temperature of the prepared coating solution can be freely set in the range of −30 ° C. or higher and 50 ° C. or lower. When the coating solution contains a compound that tends to precipitate, the temperature can be set higher, and when a compound that tends to thicken is contained, storage at a low temperature can prevent the solution from deteriorating. In the present invention, it is usually most preferably 20 ° C. or less, preferably 15 ° C. or less, more preferably 10 ° C. or less and 5 ° C. or less. As the temperature of the liquid is lower, the decomposition of the charge transport material can be suppressed.

<Conductive support>
As the conductive support used in the electrophotographic photosensitive member of the present invention, for example, metal materials such as aluminum, aluminum alloy, stainless steel, copper and nickel, and conductive powders such as metal, carbon and tin oxide are added. Mainly used are resin materials provided with conductivity and resins, glass, paper, and the like obtained by depositing or coating a conductive material such as aluminum, nickel, ITO (indium tin oxide) on the surface. As a form, a drum shape, a sheet shape, a belt shape or the like is used. A conductive material having an appropriate resistance value may be applied to a conductive support made of a metal material in order to control conductivity, surface properties, etc. or to cover defects.

When a metal material such as an aluminum alloy is used as the conductive support, it may be used after an anodized film is applied. When an anodized film is applied, it is desirable to perform a sealing treatment by a known method. For example, an anodic oxidation film is formed by anodizing in an acidic bath such as chromic acid, sulfuric acid, oxalic acid, boric acid, sulfamic acid, etc. give. In the case of anodic oxidation in sulfuric acid, the sulfuric acid concentration is 100 g / L to 300 g / L, the dissolved aluminum concentration is 2 g / L to 15 g / L, the liquid temperature is 15 ° C. to 30 ° C., the electrolysis voltage is 10 V to 20 V, and the current density. Is preferably set within the range of 0.5 A / dm ^{2 to 2} A / dm ² , but is not limited to the above conditions.

  It is preferable to perform a sealing treatment on the anodic oxide film thus formed. The sealing treatment may be performed by a known method. For example, it is immersed in an aqueous solution containing nickel fluoride as a main component, or immersed in an aqueous solution containing nickel acetate as a main component. A high temperature sealing treatment is preferably performed.

  The concentration of the nickel fluoride aqueous solution used in the case of the low-temperature sealing treatment can be selected as appropriate, but more preferable results are obtained when it is used in the range of 3 g / L to 6 g / L. In order to smoothly proceed with the sealing treatment, the treatment temperature is 25 ° C. to 40 ° C., preferably 30 ° C. to 35 ° C., and the pH of the nickel fluoride aqueous solution is 4.5 to 6.5, preferably Is preferably processed in the range of 5.5 to 6.0. As the pH adjuster, oxalic acid, boric acid, formic acid, acetic acid, sodium hydroxide, sodium acetate, aqueous ammonia and the like can be used. The treatment time is preferably in the range of 1 minute to 3 minutes per 1 μm of film thickness. In order to further improve the physical properties of the film, cobalt fluoride, cobalt acetate, nickel sulfate, a surfactant or the like may be added to the nickel fluoride aqueous solution. Subsequently, it is washed with water and dried to finish the low temperature sealing treatment.

  As the sealing agent in the case of the high-temperature sealing treatment, an aqueous solution of a metal salt such as nickel acetate, cobalt acetate, lead acetate, nickel acetate-cobalt, and barium nitrate can be used, and it is particularly preferable to use nickel acetate. . The concentration in the case of using an aqueous nickel acetate solution is preferably in the range of 5 g / L to 20 g / L. The treatment temperature is 80 ° C. to 100 ° C., preferably 90 ° C. to 98 ° C., and the pH of the nickel acetate aqueous solution is preferably 5.0 to 6.0.

  Here, aqueous ammonia, sodium acetate, or the like can be used as the pH adjuster. The treatment time is 10 minutes or longer, preferably 20 minutes or longer. In this case as well, sodium acetate, organic carboxylic acid, anionic and nonionic surfactants may be added to the nickel acetate aqueous solution in order to improve the film properties. Subsequently, it is washed with water and dried to finish the high temperature sealing treatment. When the average film thickness is thick, stronger sealing conditions are required due to the higher concentration of the sealing liquid and high temperature / long-time treatment. Accordingly, productivity is deteriorated and surface defects such as spots, dirt, and dusting are likely to occur on the coating surface. From such a point, it is preferable that the average film thickness of the anodic oxide coating is usually 20 μm or less, particularly 7 μm or less.

  The support surface may be smooth, or may be roughened by using a special cutting method or polishing. Further, it may be roughened by mixing particles having an appropriate particle diameter with the material constituting the support. In order to reduce the cost, it is possible to use the drawing tube as it is without cutting. Especially when using a non-cutting aluminum support such as drawing, impact, or ironing, the process eliminates dirt, foreign matter, and other flaws, small scratches, etc., and provides a uniform and clean support. Therefore, it is preferable.

<Underlayer>
An undercoat layer may be provided between the conductive support and the photosensitive layer in order to improve adhesion and blocking properties. As the undercoat layer, a resin, a resin in which particles such as a metal oxide are dispersed, or the like is used. The undercoat layer may be a single layer or a plurality of layers.

  Examples of metal oxide particles used for the undercoat layer include metal oxide particles containing one metal element such as titanium oxide, aluminum oxide, silicon oxide, zirconium oxide, zinc oxide, iron oxide, calcium titanate, titanium Examples thereof include metal oxide particles containing a plurality of metal elements such as strontium acid and barium titanate. One kind of these particles may be used alone, or a plurality of kinds of particles may be mixed and used in an arbitrary combination and ratio.

Among these metal oxide particles, titanium oxide and aluminum oxide are preferable, and titanium oxide is particularly preferable.
The surface of the titanium oxide particles may be treated with an inorganic substance such as tin oxide, aluminum oxide, antimony oxide, zirconium oxide, or silicon oxide, or an organic substance such as stearic acid, polyol, or silicone. Any one of these treatments may be used, or two or more thereof may be applied.

  As the crystal form of the titanium oxide particles, any of rutile, anatase, brookite, and amorphous can be used. The titanium oxide particles may have only one crystal type, or may contain two or more crystal types in any combination and ratio.

  Various particle sizes can be used as the particle size of the metal oxide particles. Among them, the average primary particle size is usually 10 nm or more from the viewpoint of the properties of the binder resin, etc., which is the raw material for the undercoat layer, and the stability of the liquid. Usually, it is 100 nm or less, preferably 50 nm or less. This average primary particle size is defined by a value obtained by measurement from a TEM photograph.

  The undercoat layer is preferably formed in a form in which metal oxide particles are dispersed in a binder resin. The binder resin used for the undercoat layer is epoxy resin, polyethylene resin, polypropylene resin, acrylic resin, methacrylic resin, polyamide resin, vinyl chloride resin, vinyl acetate resin, phenol resin, polycarbonate resin, polyurethane resin, polyimide resin, chloride resin. Vinylidene resin, polyvinyl acetal resin, vinyl chloride-vinyl acetate copolymer, polyvinyl alcohol resin, polyurethane resin, polyacrylic acid resin, polyacrylamide resin, polyvinyl pyrrolidone resin, polyvinyl pyridine resin, water-soluble polyester resin, cellulose such as nitrocellulose Ester resin, cellulose ether resin, casein, gelatin, polyglutamic acid, starch, starch acetate, amino starch, zirconium chelate compound, zirconi Organic zirconium compounds of the arm alkoxide compounds, titanyl chelate compounds, organic titanyl compounds such as titanyl alkoxide compound, silane coupling agent, and the like. These may be used alone or in combination of two or more in any combination and ratio. Moreover, you may use with the hardening | curing form with the hardening | curing agent. Among these, alcohol-soluble copolymerized polyamide, modified polyamide, and the like are preferable because they exhibit good dispersibility and coating properties.

  The mixing ratio of the metal oxide particles to the binder resin used in the undercoat layer can be arbitrarily selected, but it is usually applied in the range of 10 parts by mass to 500 parts by mass with respect to 100 parts by mass of the binder resin. It is preferable in terms of liquid stability and coatability.

  When the coating solution for forming the undercoat layer contains metal oxide particles, the metal oxide particles are present dispersed in the coating solution. In order to disperse the metal oxide particles in the coating liquid, for example, it can be produced by wet dispersion in an organic solvent with a known mechanical grinding device such as a ball mill, a sand grind mill, a planetary mill, or a roll mill. However, it is preferable to disperse using a dispersion medium.

  As a dispersing device for dispersing using a dispersion medium, any known dispersing device may be used. However, a pebble mill, a ball mill, a sand mill, a screen mill, a gap mill, a vibration mill, a paint shaker, an atomizer may be used. Examples include lighters. Among these, those that can be dispersed by circulating the coating solution are preferable, and a sand mill, a screen mill, and a gap mill are used from the viewpoints of dispersion efficiency, fineness of the reached particle diameter, ease of continuous operation, and the like. The sand mill may be either a vertical type or a horizontal type. The disc shape of the sand mill can be any plate type, vertical pin type, horizontal pin type or the like.

  In order to disperse the titanium oxide particles in the coating solution for the undercoat layer, dispersion media having various particle sizes can be used, but it is preferable to use a dispersion media having an average particle size of 5 μm to 200 μm.

  Since the dispersion medium is generally in the shape of a perfect sphere, the average particle diameter can be obtained by a method of sieving with a sieve described in, for example, JIS Z 8801: 2000 or by image analysis. The density can be measured by the method. Specifically, for example, an average particle diameter and sphericity can be measured by an image analyzer represented by LUZEX50 manufactured by Nireco Corporation. The average particle size of the dispersion medium is usually 5 μm to 200 μm, and preferably 10 μm to 100 μm. In general, a dispersion medium having a small particle diameter tends to give a uniform dispersion in a short time. However, if the particle diameter is excessively small, the mass of the dispersion medium becomes too small to perform efficient dispersion.

The density of the dispersion medium is usually 5.5 g / cm ³ or more, preferably 5.9 g / cm ³ or more, more preferably 6.0 g / cm ³ or more. Generally, dispersion using a higher density dispersion medium tends to give a uniform dispersion in a shorter time. The sphericity of the dispersion medium is preferably 1.08 or less, more preferably a dispersion medium having a sphericity of 1.07 or less.

  The material of the dispersion medium is insoluble in the coating solution for forming the undercoat layer, and has a specific gravity larger than that of the coating solution for forming the undercoat layer. Any known dispersion medium can be used as long as it does not alter the forming coating solution, and steel balls such as chrome balls (ball balls for ball bearings) and carbon balls (carbon steel balls); stainless steel balls; Ceramic spheres such as silicon nitride spheres, silicon carbide, zirconia, and alumina; spheres coated with a film of titanium nitride, titanium carbonitride, etc. are mentioned. Among these, ceramic spheres are preferable, and zirconia fired balls are particularly preferable. . More specifically, it is particularly preferable to use zirconia fired beads described in Japanese Patent No. 3400836.

  As disclosed in Japanese Patent Application Laid-Open No. 2007-334335, the metal oxide particles have a volume average particle size of 0.1 μm or less, preferably measured by a dynamic light scattering method in the undercoat layer measurement dispersion. Is 95 nm or less, more preferably 90 nm or less. Moreover, although there is no restriction | limiting in the minimum of the said volume average particle diameter, Usually, it is 20 nm or more. By satisfying the above range, the electrophotographic photosensitive member of the present invention has stable exposure-charging repeat characteristics under low temperature and low humidity, and suppresses occurrence of image defects such as black spots and color spots in the obtained image. it can.

  Similarly, as disclosed in Japanese Patent Application Laid-Open No. 2007-334335, the metal oxide particles have a cumulative 90% particle diameter of 0.3 μm measured by the dynamic light scattering method in the undercoat layer measurement dispersion. Below, it is preferably 0.25 μm or less, more preferably 0.2 μm or less. The lower limit of the cumulative 90% particle diameter is not limited, but is usually 10 nm or more, preferably 20 nm or more, more preferably 50 nm or more. In a conventional electrophotographic photoreceptor, a metal oxide particle aggregate that is large enough to penetrate the front and back of the undercoat layer is formed by aggregation of metal oxide particles in the undercoat layer, and the large metal oxide particles The agglomerates could cause defects during image formation. Further, when a contact type is used as the charging means, when the photosensitive layer is charged, the charge moves from the photosensitive layer to the conductive support through the metal oxide particles, and the charging is appropriately performed. There was also a possibility that it could not be done. However, in the electrophotographic photosensitive member of the present invention, since the cumulative 90% particle diameter is very small, there are very few large metal oxide particles that cause defects as described above. As a result, in the electrophotographic photosensitive member of the present invention, it is possible to suppress the occurrence of defects and the inability to appropriately charge, and high-quality image formation is possible.

  The thickness of the undercoat layer can be arbitrarily selected, but it is usually 0 from the viewpoint of improving the electrical characteristics, strong exposure characteristics, image characteristics, and repeat characteristics of the electrophotographic photosensitive member, and the applicability during production. 0.01 μm or more, preferably 0.1 μm or more, and usually 30 μm or less, preferably 20 μm or less.

<Charge generating material>
The photosensitive layer formed on the conductive support may have a single layer structure in which the charge generation material and the charge transport material are present in the same layer and dispersed in the binder resin, or the charge generation material may be Any of a layered structure in which the charge generation layer dispersed in the binder and the charge transport material are functionally separated into the charge transport layer dispersed in the binder resin may be used. In the present invention, it is preferable to use a dye / pigment as a charge generating substance, if necessary. Specific examples include selenium and its alloys, cadmium sulfide, other inorganic photoconductive materials, phthalocyanine pigments, azo pigments, dithioketopyrrolopyrrole pigments, squalene pigments, quinacridone pigments, indigo pigments, perylene pigments, polycyclic quinones. Various photoconductive materials such as organic pigments such as pigments, anthanthrone pigments, and benzimidazole pigments can be used, and organic pigments, phthalocyanine pigments, and azo pigments are particularly preferable.

  Specific examples of the phthalocyanine used include metal-free phthalocyanine, copper, indium, gallium, tin, titanium, zinc, vanadium, silicon, germanium, and other metals, or oxides, halides, hydroxides, and alkoxides thereof. Various crystal forms of such coordinated phthalocyanines are used. In particular, titanyl phthalocyanines (also known as oxytitanium) such as X-type, τ-type metal-free phthalocyanine, A-type (also known as β-type), B-type (also known as α-type), and D-type (also known as Y-type), which are highly sensitive crystal types Phthalocyanine), vanadyl phthalocyanine, chloroindium phthalocyanine, chlorogallium phthalocyanine such as type II, hydroxygallium phthalocyanine such as type V, μ-oxo-gallium phthalocyanine dimer such as type G and I, μ-oxo such as type IIS -Aluminum phthalocyanine dimer is preferred. Of these phthalocyanines, A-type (β-type), B-type (α-type), D-type (Y-type) oxytitanium phthalocyanine, II-type chlorogallium phthalocyanine, V-type hydroxygallium phthalocyanine, G-type μ-oxo- Gallium phthalocyanine dimer and the like are particularly preferable. In particular, oxytitanium phthalocyanine preferably has a clear diffraction peak mainly at a Bragg angle (2θ ± 0.2 °) of 27.3 ° in a powder X-ray diffraction spectrum by CuKα characteristic X-ray.

  Further, the oxytitanium phthalocyanine preferably has a clear diffraction peak at a Bragg angle (2θ ± 0.2 °) of 9.0 ° to 9.7 ° in a powder X-ray diffraction spectrum by CuKα characteristic X-ray. .

  In the oxytitanium phthalocyanine, the chlorine content in the crystal is preferably 1.5% by mass or less. The chlorine content is determined from elemental analysis.

  Further, in the oxytitanium phthalocyanine crystal, the ratio of the chlorinated oxytitanium phthalocyanine represented by the following formula (13) is higher than the unsubstituted oxytitanium phthalocyanine represented by the following formula (14). The ratio is 0.070 or less. The mass spectral intensity ratio is preferably 0.060 or less, more preferably 0.055 or less. In the production, when the dry grinding method is used for amorphization, 0.02 or more is preferable, and when the acid paste method is used for amorphization, 0.03 or less is preferable. The amount of chlorine substitution is measured based on the technique disclosed in Japanese Patent Application Laid-Open No. 2001-115054.

  The particle size of these oxytitanyl phthalocyanines varies greatly depending on the production method and the crystal conversion method, but considering the dispersibility, the primary particle size is preferably 500 nm or less, and from the viewpoint of coating film formability, it is preferably 300 nm or less. .

  The oxytitanium phthalocyanine may contain, for example, a fluorine atom, a nitro group, or a cyano group in addition to the chlorinated oxytitanium phthalocyanine. Alternatively, various oxytitanium phthalocyanine derivatives substituted with a substituent such as a sulfone group may be contained.

As the azo pigment, various known bisazo pigments and trisazo pigments are preferably used. An example of a preferable azo pigment is shown in the following formula (15). In the following formula (15), Cp ¹ to Cp ³ represent a coupler.

In the above formula (15), the following structures are preferable as the couplers Cp ¹ to Cp ³ .

フタロシアニンとアゾ顔料を併用することによって、高感度かつゴーストのない感光体を作製することが可能である。

By using phthalocyanine and an azo pigment in combination, it is possible to produce a highly sensitive and ghost-free photoreceptor.

  Examples of the binder resin used for the charge generation layer in the function-separated photoreceptor include polyvinyl butyral resin, polyvinyl formal resin, partially acetalized polyvinyl butyral resin in which a part of butyral is modified with formal, acetal, etc. Polyvinyl acetal resin, polyarylate resin, polycarbonate resin, polyester resin, modified ether polyester resin, phenoxy resin, polyvinyl chloride resin, polyvinylidene chloride resin, polyvinyl acetate resin, polystyrene resin, acrylic resin, methacrylic resin, polyacrylamide Resin, polyamide resin, polyvinyl pyridine resin, cellulose resin, polyurethane resin, epoxy resin, silicone resin, polyvinyl alcohol resin, polyvinyl pyrrolidone resin, casein, chloride Vinyl chloride-vinyl acetate, such as nyl-vinyl acetate copolymer, hydroxy-modified vinyl chloride-vinyl acetate copolymer, carboxyl-modified vinyl chloride-vinyl acetate copolymer, vinyl chloride-vinyl acetate-maleic anhydride copolymer Copolymer, styrene-butadiene copolymer, vinylidene chloride-acrylonitrile copolymer, styrene-alkyd resin, silicone-alkyd resin, phenol-formaldehyde resin and other insulating resins, poly-N-vinylcarbazole, polyvinylanthracene, It can be selected from organic photoconductive polymers such as polyvinyl perylene, but is not limited to these polymers. These binder resins may be used alone or in combination of two or more.

  Solvents and dispersion media used to dissolve the binder resin and prepare the coating solution include, for example, saturated aliphatic solvents such as pentane, hexane, octane, and nonane, aromatic solvents such as toluene, xylene, and anisole, chlorobenzene Halogenated aromatic solvents such as dichlorobenzene and chloronaphthalene, amide solvents such as dimethylformamide and N-methyl-2-pyrrolidone, alcohol solvents such as methanol, ethanol, isopropanol, n-butanol and benzyl alcohol, glycerin Aliphatic polyhydric alcohols such as polyethylene glycol, chain, branched and cyclic ketone solvents such as acetone, cyclohexanone, methyl ethyl ketone, 4-methoxy-4-methyl-2-pentanone, methyl formate, ethyl acetate, n-acetate Ester solvents such as butyl, Halogenated hydrocarbon solvents such as methylene chloride, chloroform, 1,2-dichloroethane, chain and cyclic ether solvents such as diethyl ether, dimethoxyethane, tetrahydrofuran, 1,4-dioxane, methyl cellosolve, ethyl cellosolve, Aprotic polar solvents such as acetonitrile, dimethyl sulfoxide, sulfolane, hexamethylphosphoric triamide, n-butylamine, isopropanolamine, diethylamine, triethanolamine, nitrogen-containing compounds such as ethylenediamine, triethylenediamine, triethylamine, mineral oil such as ligroin, Examples thereof include water, and those that do not dissolve the above-described undercoat layer are preferably used. These can be used alone or in combination of two or more.

  In the charge generation layer of the function-separated type photoreceptor, the compounding ratio (mass ratio) of the binder resin and the charge generation material is 10 parts by mass to 1000 parts by mass, preferably 30 parts by mass with respect to 100 parts by mass of the binder resin. It is the range of -500 mass parts, The film thickness is 0.1 micrometer-4 micrometers normally, Preferably it is 0.15 micrometer-0.6 micrometer. If the ratio of the charge generation material is too high, the stability of the coating solution is lowered due to problems such as aggregation of the charge generation material, while if it is too low, the sensitivity as a photoconductor is reduced. It is preferable to do this. As a method for dispersing the charge generation material, a known dispersion method such as a ball mill dispersion method, an attritor dispersion method, a sand mill dispersion method, or an ultrasonic dispersion method can be used. At this time, it is effective to make the particles finer to a particle size of 0.5 μm or less, preferably 0.3 μm or less, more preferably 0.15 μm or less.

<Charge transport material>
In the present invention, when the above-described enamine compound or butadiene compound is used as the charge transport material, the remarkable effect of the acid scavenger can be obtained, but any other known charge transport material can be used in combination. is there. Examples of known charge transport materials include aromatic nitro compounds such as 2,4,7-trinitrofluorenone, cyano compounds such as tetracyanoquinodimethane, electron withdrawing materials such as quinone compounds such as diphenoquinone, and carbazole derivatives. , Indole derivatives, imidazole derivatives, oxazole derivatives, pyrazole derivatives, thiadiazole derivatives, heterocyclic compounds such as benzofuran derivatives, aniline derivatives, hydrazone derivatives, aromatic amine derivatives, stilbene derivatives, and a combination of these compounds. Alternatively, an electron donating substance such as a polymer having a group consisting of these compounds in the main chain or side chain may be used. Among these, a carbazole derivative, an aromatic amine derivative, a stilbene derivative, a hydrazone derivative, and a combination of these compounds are preferable. Any one of these charge transport materials may be used alone, or two or more thereof may be used in any combination. In the case where an enamine compound or a butadiene compound is used in combination with another known charge transport material, the content ratio of the charge transport material to be used in the total amount of the charge transport material is not particularly limited, but is 20% by mass or less. Is preferable, and it is more preferable that it is 10 mass% or less.

  Specific examples of suitable structures of the charge transport material are shown below. In the following compounds, R ′ may be the same or different. R ′ is preferably a hydrogen atom, an alkyl group, an alkoxy group, a phenyl group, or an arylalkyl, and particularly preferably a methyl group, an ethyl group, or a benzyl group. N is an integer of 0 to 2. These specific examples are shown for illustration, and any known charge transporting material may be used as long as it does not contradict the gist of the present invention.

<Binder resin>
When forming a charge transport layer of a function-separated type photoreceptor having a charge generation layer and a charge transport layer and a photosensitive layer of a single layer type photoreceptor, a binder resin is used to ensure film strength and to disperse the compound. Is done. In the case of the charge transport layer of the function-separated type photoreceptor, it can be obtained by applying and drying a coating solution obtained by dissolving or dispersing a charge transport material and various binder resins in a solvent. In the case of a single-layer type photoreceptor, it can be obtained by applying and drying a coating solution obtained by dissolving or dispersing a charge generating substance, a charge transporting substance and various binder resins in a solvent. Examples of the binder resin include polymers and copolymers of vinyl compounds such as butadiene resin, styrene resin, vinyl acetate resin, vinyl chloride resin, acrylic ester resin, methacrylic ester resin, vinyl alcohol resin, and ethyl vinyl ether, polyvinyl Butyral resin, polyvinyl formal resin, partially modified polyvinyl acetal, polycarbonate resin, polyester resin, polyarylate resin, polyamide resin, polyurethane resin, cellulose ester resin, phenoxy resin, silicone resin, silicone-alkyd resin, poly-N-vinylcarbazole resin Etc. These resins may be modified with a silicon reagent or the like. Of the above binder resins, polycarbonate resins or polyarylate resins are preferred.

Among the polycarbonate resins and polyarylate resins, the following bisphenol or polycarbonate resins and polyarylate resins containing a biphenol component are preferable from the viewpoint of sensitivity and residual potential, and among them, the polycarbonate resin is more preferable from the viewpoint of mobility.
Polycarbonate resins and polyarylate resins generally have a partial structure of a diol component. Examples of the diol component that forms these structures include bisphenol compounds and biphenol compounds.

Specific examples thereof include 4,4′-biphenol, 3,3′-dimethyl-4,4′-dihydroxy-1,1′-biphenyl, 3,3′-di (t-butyl) -4,4 ′. -Dihydroxy-1,1'-biphenyl, 3,3 ', 5,5'-tetramethyl-4,4'-dihydroxy-1,1'-biphenyl, 3,3', 5,5'-tetra (t -Butyl) -4,4'-dihydroxy-1,1'-biphenyl, 2,2 ', 3,3', 5,5'-hexamethyl-4,4'-dihydroxy-1,1'-biphenyl, 2, , 4′-biphenol, 3,3′-dimethyl-2,4′-dihydroxy-1,1′-biphenyl, 3,3′-di (t-butyl) -2,4′-dihydroxy-1,1 ′ -Biphenyl, 2,2'-biphenol, 3,3'-dimethyl-2,2'-dihydroxy-1,1'-biphenyl, 3,3'-di Biphenol compounds such as t- butyl) -2,2'-dihydroxy-1,1'-biphenyl;
Bis (4-hydroxyphenyl) methane, 1,1-bis (4-hydroxyphenyl) ethane, 1,1-bis (4-hydroxyphenyl) propane, 2,2-bis (4-hydroxyphenyl) propane, 1, 1-bis (4-hydroxyphenyl) butane, 2,2-bis (4-hydroxyphenyl) butane, 1,1-bis (4-hydroxyphenyl) pentane, 2,2-bis (4-hydroxyphenyl) pentane, 3,3-bis (4-hydroxyphenyl) pentane, 2,2-bis (4-hydroxyphenyl) -3-methylbutane, 1,1-bis (4-hydroxyphenyl) hexane, 2,2-bis (4- Hydroxyphenyl) hexane, 3,3-bis (4-hydroxyphenyl) hexane, 2,2-bis (4-hydroxyphenyl) -4-methyl Pentane, 1,1-bis (4-hydroxyphenyl) cyclopentane, 1,1-bis (4-hydroxyphenyl) bisphenol compounds having no substituents on the aromatic rings such as cyclohexane;
Bis (3-phenyl-4-hydroxyphenyl) methane, 1,1-bis (3-phenyl-4-hydroxyphenyl) ethane, 1,1-bis (3-phenyl-4-hydroxyphenyl) propane, 2,2 A bisphenol compound having an aryl group as a substituent on an aromatic ring such as bis (3-phenyl-4-hydroxyphenyl) propane;
Bis (4-hydroxy-3-methylphenyl) methane, 1,1-bis (4-hydroxy-3-methylphenyl) ethane, 1,1-bis (4-hydroxy-3-methylphenyl) propane, 2,2 -Bis (4-hydroxy-3-methylphenyl) propane, 1,1-bis (4-hydroxy-3-methylphenyl) cyclohexane, etc.
Bis (4-hydroxy-3-ethylphenyl) methane, 1,1-bis (4-hydroxy-3-ethylphenyl) ethane, 1,1-bis (4-hydroxy-3-ethylphenyl) propane, 2,2 -Bis (4-hydroxy-3-ethylphenyl) propane, 1,1-bis (4-hydroxy-3-ethylphenyl) cyclohexane, etc.
2,2-bis (4-hydroxy-3-isopropylphenyl) propane, 2,2-bis (4-hydroxy-3- (sec-butyl) phenyl) propane, bis (4-hydroxy-3,5-dimethylphenyl) ) Methane, 1,1-bis (4-hydroxy-3,5-dimethylphenyl) ethane, 2,2-bis (4-hydroxy-3,5-dimethylphenyl) propane, 1,1-bis (4-hydroxy) -3,5-dimethylphenyl) cyclohexane, bis (4-hydroxy-3,6-dimethylphenyl) methane, 1,1-bis (4-hydroxy-3,6-dimethylphenyl) ethane, 2,2-bis ( 4-hydroxy-3,6-dimethylphenyl) propane, bis (4-hydroxy-2,3,5-trimethylphenyl) methane, 1,1-bis (4-hydride) Xyl-2,3,5-trimethylphenyl) ethane, 2,2-bis (4-hydroxy-2,3,5-trimethylphenyl) propane, bis (4-hydroxy-2,3,5-trimethylphenyl) phenyl On aromatic rings such as methane, 1,1-bis (4-hydroxy-2,3,5-trimethylphenyl) phenylethane, 1,1-bis (4-hydroxy-2,3,5-trimethylphenyl) cyclohexane A bisphenol compound having an alkyl group as a substituent;
Bis (4-hydroxyphenyl) (phenyl) methane, 1,1-bis (4-hydroxyphenyl) -1-phenylethane, 1,1-bis (4-hydroxyphenyl) -1-phenylpropane, bis (4- A bisphenol compound in which a divalent group connecting aromatic rings such as hydroxyphenyl) (diphenyl) methane and bis (4-hydroxyphenyl) (dibenzyl) methane has an aryl group as a substituent;

  The structure of bisphenol and biphenol that can be suitably used for the polycarbonate resin is exemplified below. This illustration is made for the purpose of clarifying the gist of the present invention, and is not limited to the illustrated structure unless it is contrary to the gist of the present invention.

  In particular, in order to maximize the effects of the present invention, a polycarbonate having bisphenol and biphenol having the following structures as repeating units is preferred.

  The polyarylate resin suitable for the present invention has a repeating structure represented by the general formula (A).

In formula (A), Ar ^{a1 to} Ar ^a4 each independently represent an arylene group which may have a substituent, X and Y each represent a single bond or a divalent group, and k represents an integer of 0 or more. Represent.
In formula (A), Ar ^{a1 to} Ar ^a4 each independently represent an arylene group which may have a substituent. Examples of the arylene group include 1,2-phenylene group, 1,3-phenylene group, 1,4-phenylene group, naphthylene group, anthrylene group, and phenanthrylene group. From the viewpoint of electrical characteristics, 1,4-phenylene group Is preferred.

Moreover, the arylene group which comprises Ar < ^a1 > -Ar < ^a4 > may have a substituent each independently. Specific examples of the substituent include an alkyl group, an aryl group, a halogen group, and an alkoxy group. Of these, considering the mechanical properties as the binder resin for the photosensitive layer and the solubility in the coating solution for forming the photosensitive layer, the alkyl group is preferably a methyl group, an ethyl group, a propyl group, an isopropyl group, or the like. The group is preferably a phenyl group, a naphthyl group, etc., the halogen group is preferably a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, etc., and the alkoxy group is preferably a methoxy group, an ethoxy group, a propoxy group, a butoxy group, etc. Is done. In addition, when a substituent is an alkyl group, carbon number of the alkyl group is usually 1 or more, and usually 10 or less, preferably 8 or less, more preferably 2 or less.

Ar ^{a1 to} Ar ^a2 each preferably have 0 to 2 substituents, preferably have a substituent from the viewpoint of adhesion, and further have one substituent from the viewpoint of wear resistance. It is preferable. Further, the substituent is preferably an alkyl group, and most preferably a methyl group.
Ar ^{a3 to} Ar ^a4 each preferably have 0 to 2 substituents, and preferably have no substituent from the viewpoint of wear resistance.

In the formula (A), X and Y each independently represent a single bond or a divalent group. Preferable examples of X and Y include a sulfur atom, an oxygen atom, a sulfonyl group, a cycloalkylidene group, —CR ⁴⁴ R ⁴⁵ — and the like. Here, R ⁴⁴ and R ⁴⁵ each independently represent a hydrogen atom, an alkyl group, an aryl group, a halogen group, or an alkoxy group. Further, among R ⁴⁴ and R ⁴⁵ , considering the mechanical properties as a binder resin for the photosensitive layer and the solubility in the coating solution for forming the photosensitive layer, the alkyl group may be a methyl group, an ethyl group, a propyl group, An isopropyl group or the like is preferable, a phenyl group or a naphthyl group is preferable as an aryl group, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom or the like is preferable as a halogen group, and a methoxy group, an ethoxy group or a propoxy group as an alkoxy group And a butoxy group are preferred. In addition, when ^R44 or ^R45 is an alkyl group, carbon number of the alkyl group is usually 1 or more, and usually 10 or less, preferably 8 or less, more preferably 2 or less.

Further, considering the simplicity of production of the divalent hydroxy compound used for producing the resin, examples of preferable groups as X include —O—, —S—, cyclohexylidene, —CR ⁴⁴ R ⁴⁵ —. Is mentioned. Among them, X is preferably —CR ⁴⁴ R ⁴⁵ —, R ⁴⁴ and R ⁴⁵ are preferably a hydrogen atom or an alkyl group, and at least one of R ⁴⁴ and R ⁴⁵ is a hydrogen atom. Most preferred in terms of wear resistance.

Further, considering the simplicity of production of the divalent hydroxy compound used for producing the resin, examples of a group preferable as Y include a single bond, —O—, —S—, and —CH ₂ —. . From the viewpoint of wear resistance, a divalent group having 3 or less atoms is preferable, and —O— is most preferable.
k is an integer of 0 or more, preferably 0 to 1 in consideration of the simplicity of production, and most preferably k = 1 from the viewpoint of wear resistance.

  Moreover, as a specific example of the acid component which forms a polyester resin, it is preferable to use what has the following structures.

特に好ましい酸成分は、電気特性、耐磨耗性の観点から、以下の構造を有するものである。

Particularly preferred acid components are those having the following structure from the viewpoints of electrical properties and wear resistance.

ポリエステル樹脂に用いられるジオールとしては、前記したポリカーボネート樹脂に用いられるジオールが使用可能であるが、これらの中でも特に、下記構造のジオールを繰り返し単位構造として有するポリアリレート樹脂が好ましい例をして挙げられる。

As the diol used in the polyester resin, the diol used in the above-described polycarbonate resin can be used, and among these, a polyarylate resin having a diol having the following structure as a repeating unit structure is given as a preferred example. .

これらのジカルボン酸成分やジオール成分は、複数種組み合わせて用いることも可能である。

These dicarboxylic acid components and diol components can be used in combination.

If the molecular weight of the binder resin is too low, the mechanical strength is insufficient. Conversely, if the molecular weight is too high, the viscosity of the coating solution for forming the photosensitive layer may be too high, resulting in a decrease in productivity. In the case of polycarbonate resin and polyester resin (including polyarylate resin), the viscosity average molecular weight is preferably 10,000 or more, particularly preferably 20,000 or more. Moreover, 70,000 or less is preferable, Most preferably, it is 50,000 or less. The viscosity average molecular weight is measured by the measuring method described in the examples and is defined thereby.
In the present invention, it is preferable to use a polyester resin. Polyester resins are superior in wear resistance compared to polycarbonate resins.

  The amount of the carboxylic acid group (—COOH group) present at the terminal of the polyarylate resin used in the present invention is usually 30 μeq / g or less, preferably 15 μeq / g or less, more preferably 10 μeq / g or less, particularly preferably 5 μeq / g. It is as follows. When the amount of the terminal carboxylic acid group is increased, there is a tendency that the electric characteristics are deteriorated such as an increase in surface potential, which is not preferable. Moreover, in this invention, it is possible to suppress decomposition | disassembly of charge transport material, so that the amount of terminal carboxylic acid groups is low. The amount of the terminal carboxylic acid group can be quantified by dissolving a precisely weighed polyarylate resin in benzyl alcohol and titrating with a 0.01 N NaOH benzyl alcohol solution. The amount of the terminal carboxylic acid group in the present invention is a value measured by <Method for measuring the amount of terminal carboxylic acid (—COOH) group>, and this may include an acid component such as a residual monomer in the resin. However, it is defined as the amount of terminal carboxylic acid group including them.

  The amount of nitrogen incorporated in the molecular chain of the polyarylate used in the present invention is usually 100 ppm or less, preferably 50 ppm or less, and particularly preferably 20 ppm or less. If the nitrogen content exceeds the above range, electrical characteristics such as an increase in surface potential are deteriorated, which is not preferable. The nitrogen content in the resin can be measured with a total nitrogen analyzer (TN-10) manufactured by Mitsubishi Chemical Corporation.

  The amount of the acid chloride group remaining at the terminal of the polyarylate resin is usually 1 μeq / g or less, preferably 0.3 μeq / g or less, particularly preferably 0.1 μeq / g or less. When the amount of the terminal acid chloride group exceeds the above range, the storage stability is lowered, which is not preferable. The amount of the terminal acid chloride group is obtained by dissolving a precisely weighed polyarylate resin in methylene chloride, adding a 1% by mass methylene chloride solution of 4- (p-nitrobenzyl) pyridine, and measuring the absorbance at a wavelength of 440 nm. Separately, an extinction coefficient can be obtained using a methylene chloride solution of benzoyl chloride to quantify the amount of acid chloride groups in the resin.

  Similarly, the amount of OH groups present at the end of the polyarylate resin is not usually limited, but is preferably 50 μeq / g or less, particularly preferably 20 μeq / g or less. An increase in the amount of terminal OH groups is not preferable because electric characteristics such as an increase in surface potential tend to be deteriorated. The amount of terminal OH groups can be quantified by coloring with titanium tetrachloride by acidification with acetic acid and measuring the absorbance at a wavelength of 480 nm.

  The ratio of the binder resin and the charge transport material used in the charge transport layer of the multilayer photoreceptor and the photosensitive layer of the single-layer photoreceptor is usually a charge relative to 100 parts by weight of the binder resin in both the single-layer and multilayer types. The transport material is 20 parts by mass or more, preferably 30 parts by mass or more from the viewpoint of residual potential reduction, and more preferably 40 parts by mass or more from the viewpoint of stability and charge mobility during repeated use. On the other hand, from the viewpoint of thermal stability of the photosensitive layer, it is usually 150 parts by mass or less, preferably 120 parts by mass or less from the point of compatibility between the charge transport material and the binder resin, and 100 parts by mass from the viewpoint of printing durability. Part or less is more preferable, and 80 parts by weight or less is particularly preferable from the viewpoint of scratch resistance.

  In the case of a single-layer type photoreceptor, the charge generating substance is further dispersed in the charge transport medium having the above-described blending ratio. In this case, the particle size of the charge generating material needs to be sufficiently small, and is preferably 1 μm or less, more preferably 0.5 μm or less. If the amount of the charge generating material dispersed in the photosensitive layer is too small, sufficient sensitivity may not be obtained. On the other hand, if the amount is too large, adverse effects such as a decrease in chargeability and a decrease in sensitivity may occur. For example, it is preferably used in the range of 0.1% by mass to 50% by mass, particularly preferably in the range of 1% by mass to 20% by mass.

  The film thickness of the photosensitive layer of the single-layer type photoreceptor is usually 5 μm to 100 μm, preferably 10 μm to 50 μm, and the film thickness of the charge transport layer of the sequential lamination type photoreceptor is usually 5 μm to 50 μm. Although used, it is preferably 10 μm to 45 μm from the viewpoint of long life and image stability, and more preferably 10 μm to 30 μm from the viewpoint of high resolution.

<Others>
The photosensitive layer has well-known antioxidants, plasticizers, ultraviolet absorbers, electron-withdrawing compounds to improve film-forming properties, flexibility, coating properties, stain resistance, gas resistance, light resistance, etc. Further, additives such as a leveling agent and a visible light shading agent may be contained. In addition, the photosensitive layer may contain various additives such as a leveling agent, an antioxidant, and a sensitizer for improving the coating properties as necessary. Examples of the antioxidant include hindered phenol compounds and hindered amine compounds. Examples of the light shielding agent include various dye compounds, azo compounds, and the like, and examples of the leveling agent include silicone oil and fluorine-based oil.

  Examples of phenolic antioxidants include 2,6-di-t-butylphenol, 2,6-di-t-butyl-4-ethylphenol, 2,6-di-t-butyl-4-methylphenol, 2,2′-methylenebis (6-t-butyl-4-methylphenol), 4,4′-butylidenebis (6-t-butyl-3-methylphenol), 4,4′-thiobis (6-t-butyl) -3-methylphenol), 2,2′-butylidenebis (6-t-butyl-4-methylphenol), α-tocopherol, β-tocopherol, 2,2,4-trimethyl-6-hydroxy-7-t- Butylchroman, pentaerythrityltetrakis [3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate], 2,2′-thioethylenebis [3- (3,5 -Di-t-butyl-4-hydroxyphenyl) propionate], 1,6-hexanediol bis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate], butylhydroxyanisole, dibutylhydroxy Anisole, 1- [2-{(3,5-di-butyl-4-hydroxyphenyl) propionyloxy} ethyl] -4- [3- (3,5-di-butyl-4-hydroxyphenyl) propionyloxy] -2,2,6,6-tetramethylpiperazyl, 2,4-bis- (n-octylthio) -6- (4-hydroxy-3,5-di-t-butylanilino) -1,3,5- Triazine, 1,3,5-trimethyl-2,4,6-tris (3,5-di-t-butyl-4-hydroxybenzyl) benzene, 2- (5-methyl-2- Droxyphenyl) benzotriazole, 2- (3-t-butyl-5-methyl-2-hydroxyphenyl) -5-chlorobenzotriazole, 1- [2- {3- (3,5-di-t-butyl) -4-hydroxyphenyl) propionyloxy} ethyl] -4- {3- (3,5-di-t-butyl-4-hydroxyphenyl) propionyloxy} -2,2,6,6-tetramethylpiperidine, n -Octadecyl-3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate, etc. can be mentioned.

  Among these, those having one or more t-butyl groups on the phenol ring in the molecule are preferable, and among them, those in which the t-butyl group is bonded to the position adjacent to the phenolic hydroxyl group are more preferable. Among them, the one in which two t-butyl groups are bonded to the position adjacent to the phenolic hydroxyl group is most preferable. Specific examples thereof include 2,6-di-t-butylphenol, 2,6-di-t-butyl-4-ethylphenol, 2,6-di-t-butyl-4-methylphenol, and n-octadecyl. Monophenolic antioxidants such as -3- (4'-hydroxy-3 ', 5'-di-t-butylphenyl) propionate, 2,2'-methylenebis (6-t-butyl-4-methylphenol) 1,3,5-trimethyl-2,4,6-tris (3,5-di-t-butyl-4-hydroxybenzyl) benzene, pentaerythrityltetrakis [3- (3,5-di-t- Polyphenolic antioxidants such as butyl-4-hydroxyphenyl) propionate] are preferred. By using these, an electrophotographic photoreceptor free from fogging can be produced even when used repeatedly.

  Moreover, in order to improve acid-proof gas resistance, it is possible to use the alkylamine compound which may have a well-known substituent. For example, it is effective to use compounds disclosed in JP-A-3-172852 and JP-A-2007-52408. Among these, for example, tribenzylamine can be preferably used.

  A protective layer may be provided on the outermost surface layer of the photosensitive member for the purpose of preventing the photosensitive layer from being worn out or preventing or reducing the deterioration of the photosensitive layer due to a discharge substance generated from a charger or the like. The protective layer is formed by containing a conductive material in a suitable binder resin, or a co-polymer using a compound having a charge transporting ability such as a triphenylamine skeleton as described in JP-A-9-190004. Coalescence can be used. Examples of the conductive material include aromatic amino compounds such as TPD (N, N′-diphenyl-N, N′-bis- (m-tolyl) benzidine), antimony oxide, indium oxide, tin oxide, titanium oxide, and tin oxide. -Metal oxides such as antimony oxide, aluminum oxide, and zinc oxide can be used, but are not limited thereto.

As the binder resin used for the protective layer, known resins such as polyamide resin, polyurethane resin, polyester resin, epoxy resin, polyketone resin, polycarbonate resin, polyvinyl ketone resin, polystyrene resin, polyacrylamide resin, and siloxane resin can be used. Further, a copolymer of the above resin with a skeleton having a charge transporting ability such as a triphenylamine skeleton as described in JP-A-9-190004 can also be used. The protective layer is preferably configured to have an electric resistance of 10 ⁹ to 10 ¹⁴ Ω · cm. When the electric resistance is higher than 10 ¹⁴ Ω · cm, the residual potential is increased and an image with much fogging is formed. On the other hand, when the electric resistance is lower than 10 ⁹ Ω · cm, the image is blurred and the resolution is lowered. In addition, the protective layer must be configured so as not to substantially impede transmission of light irradiated for image exposure.

  In addition, the surface layer is made of fluorine-based resin, silicone resin, polyethylene resin, polystyrene resin, etc. for the purpose of reducing frictional resistance and wear on the surface of the photoreceptor, and increasing the transfer efficiency of toner from the photoreceptor to the transfer belt and paper. May be included. Moreover, the particle | grains which consist of these resin, and the particle | grains of an inorganic compound may be included.

<Layer formation method>
Each layer constituting the photoconductor is formed by repeating a coating / drying step for each layer in sequence using a known coating method on a support with a coating solution containing the material constituting each layer.

  The coating solution for forming a layer is used in the case of a charge transport layer of a single layer type photoreceptor or a multilayer type photoreceptor, and the solid content is usually used in the range of 5% by mass to 40% by mass, but 10% by mass. It is preferable to use in the range of -35 mass%. The viscosity of the coating solution is usually in the range of 10 mPa · s to 500 mPa · s, but is preferably in the range of 50 mPa · s to 400 mPa · s.

  In the case of the charge generation layer of the multilayer photoreceptor, the solid content concentration is usually used in the range of 0.1% by mass to 15% by mass, but may be used in the range of 1% by mass to 10% by mass. More preferred. The viscosity of the coating solution is usually used in the range of 0.01 mPa · s to 20 mPa · s, more preferably in the range of 0.1 mPa · s to 10 mPa · s.

  Examples of the coating method include a dip coating method, a spray coating method, a spinner coating method, a bead coating method, a wire bar coating method, a blade coating method, a roller coating method, an air knife coating method, and a curtain coating method. Other known coating methods can also be used.

  The coating solution is preferably dried by touching at room temperature, followed by heating and drying in the temperature range of 30 ° C. to 200 ° C. for 1 minute to 2 hours with no air or air. The heating temperature may be constant or may be changed while drying.

<Image forming apparatus>
Next, an embodiment of an image forming apparatus using the electrophotographic photosensitive member of the present invention will be described with reference to FIG. However, the embodiment is not limited to the following description, and can be arbitrarily modified without departing from the gist of the present invention.

  As shown in FIG. 1, the image forming apparatus includes an electrophotographic photosensitive member 1, a charging device 2, an exposure device 3, a developing device 4, and a transfer device 5, and further includes a cleaning device 6 and a fixing device as necessary. A device 7 is provided.

  The electrophotographic photoreceptor 1 is not particularly limited as long as it is the above-described electrophotographic photoreceptor of the present invention, but in FIG. 1, as an example, a drum in which the above-described photosensitive layer is formed on the surface of a cylindrical conductive support. The photoconductor is shown. A charging device 2, an exposure device 3, a developing device 4, a transfer device 5, and a cleaning device 6 are arranged along the outer peripheral surface of the electrophotographic photoreceptor 1.

  The charging device 2 charges the electrophotographic photosensitive member 1 and uniformly charges the surface of the electrophotographic photosensitive member 1 to a predetermined potential. In FIG. 1, a roller type charging device (charging roller) is shown as an example of the charging device 2, but a corona charging device such as a corotron or a scorotron, a contact type charging device such as a charging brush, etc. are often used.

  In many cases, the electrophotographic photosensitive member 1 and the charging device 2 are designed to be removable from the main body of the image forming apparatus as a cartridge having both of them (hereinafter, referred to as a photosensitive cartridge as appropriate). It is preferable to use in such a form.

  In the present invention, as described above, when the charging unit is disposed in contact with the electrophotographic photosensitive member, particularly in the case of the contact charging method in which an AC voltage is superimposed, the effect is remarkably exhibited.

  For example, when the electrophotographic photoreceptor 1 or the charging device 2 deteriorates, the photoreceptor cartridge can be removed from the image forming apparatus main body, and another new photosensitive cartridge can be mounted on the image forming apparatus main body. ing. Also, in many cases, the toner described later is stored in the toner cartridge and designed to be removable from the main body of the image forming apparatus, and when the toner in the used toner cartridge runs out, the toner cartridge is removed. It can be removed from the main body of the image forming apparatus and another new toner cartridge can be mounted. Further, a cartridge equipped with all of the electrophotographic photosensitive member 1, the charging device 2, and toner may be used.

  The type of the exposure apparatus 3 is not particularly limited as long as it can expose the electrophotographic photoreceptor 1 to form an electrostatic latent image on the photosensitive surface of the electrophotographic photoreceptor 1. Specific examples include halogen lamps, fluorescent lamps, lasers such as semiconductor lasers and He—Ne lasers, LEDs, and the like. Further, exposure may be performed by a photoreceptor internal exposure method. The light used for the exposure is arbitrary, but the exposure may be performed with, for example, monochromatic light with a wavelength of 780 nm, monochromatic light with a wavelength slightly shorter than 600 nm to 700 nm, or monochromatic light with a short wavelength of 380 nm to 600 nm. . In order to increase the resolution, among these, it is preferable to expose with a monochromatic light having a short wavelength of 380 nm to 600 nm, and more preferably to expose with a monochromatic light having a wavelength of 380 nm to 500 nm.

  The type of the developing device 4 is not particularly limited, and any device such as a dry development method such as cascade development, one-component conductive toner development, two-component magnetic brush development, or a wet development method can be used. In FIG. 1, the developing device 4 includes a developing tank 41, an agitator 42, a supply roller 43, a developing roller 44, and a regulating member 45, and is configured to store toner T inside the developing tank 41. Further, a replenishing device (not shown) for replenishing the toner T may be attached to the developing device 4 as necessary. This replenishing device is configured to be able to replenish toner T from a container such as a bottle or a cartridge.

  The supply roller 43 is formed from a conductive sponge or the like. The developing roller 44 is made of a metal roll such as iron, stainless steel, aluminum, or nickel, or a resin roll obtained by coating such a metal roll with a silicone resin, a urethane resin, a fluororesin, or the like. The surface of the developing roller 44 may be smoothed or roughened as necessary.

  The developing roller 44 is disposed between the electrophotographic photosensitive member 1 and the supply roller 43 and is in contact with the electrophotographic photosensitive member 1 and the supply roller 43, respectively. The supply roller 43 and the developing roller 44 are rotated by a rotation drive mechanism (not shown). The supply roller 43 carries the stored toner T and supplies it to the developing roller 44. The developing roller 44 carries the toner T supplied by the supply roller 43 and contacts the surface of the electrophotographic photosensitive member 1. Here, an example of a contact method is shown, but there is also a non-contact method, and jumping development is mentioned.

  The regulating member 45 is formed of a resin blade such as a silicone resin or a urethane resin, a metal blade such as stainless steel, aluminum, copper, brass, phosphor bronze, or a blade obtained by coating such a metal blade with a resin. The regulating member 45 abuts on the developing roller 44 and is pressed against the developing roller 44 side with a predetermined force by a spring or the like (general blade linear pressure is 5 g / cm to 500 g / cm). If necessary, the regulating member 45 may be provided with a function of imparting charging to the toner T by frictional charging with the toner T.

  The agitator 42 is rotated by a rotation driving mechanism, and agitates the toner T and conveys the toner T to the supply roller 43 side. A plurality of agitators 42 may be provided with different blade shapes and sizes.

  The type of the toner T is arbitrary, and in addition to the powdery toner, a polymerized toner using a suspension polymerization method, an emulsion polymerization method, or the like can be used. In particular, when a polymerized toner is used, a toner having a small particle diameter of about 4 μm to 8 μm is preferable, and the toner particles are used in a variety of shapes from a nearly spherical shape to a shape outside the spherical shape on the potato. be able to. The polymerized toner is excellent in charging uniformity and transferability and is suitably used for high image quality.

  In the present invention, the toner is particularly preferably a toner obtained by an emulsion polymerization aggregation method. Hereinafter, physical property values measured by the method disclosed in Japanese Patent Application Laid-Open No. 2007-213050 will be described. The average circularity is usually 0.950 or more, preferably 0.960 or more, more preferably 0.970 or more, and particularly preferably 0.980 or more. The upper limit of the average circularity is not limited as long as it is 1.000 or less, but is preferably 0.998 or less, more preferably 0.995 or less from the viewpoint of ease of production. The volume average particle size [Dv] is not limited and is arbitrary as long as the effects of the present invention are not significantly impaired, but is usually 4 μm or more, preferably 5 μm or more, and usually 10 μm or less, preferably 8 μm or less. If the volume average particle diameter [Dv] of the toner is too small, the stability of the image quality may be lowered, and if it is too large, the resolution may be lowered. The value [Dv / Dn] obtained by dividing the volume average particle size [Dv] by the number average particle size [Dn] is usually 1.0 or more, and usually 1.25 or less, preferably 1.20 or less, more preferably It is desirable that it is 1.15 or less. The value of [Dv / Dn] represents the state of particle size distribution, and the closer this value is to 1.0, the sharper the particle size distribution. A sharper particle size distribution is desirable because the chargeability of the toner becomes uniform.

  The type of the transfer device 5 is not particularly limited, and an apparatus using an arbitrary system such as an electrostatic transfer method such as corona transfer, roller transfer, or belt transfer, a pressure transfer method, or an adhesive transfer method can be used. . Here, it is assumed that the transfer device 5 includes a transfer charger, a transfer roller, a transfer belt, and the like disposed so as to face the electrophotographic photoreceptor 1. The transfer device 5 applies a predetermined voltage value (transfer voltage) having a polarity opposite to the charging potential of the toner T, and transfers the toner image formed on the electrophotographic photosensitive member 1 to a transfer material (paper, medium) P. Is. In the present invention, it is effective when the transfer device 5 is placed in contact with the photoreceptor via a transfer material. The method of transferring to paper after passing through a medium such as a transfer belt is called an intermediate transfer method.

  There is no restriction | limiting in particular about the cleaning apparatus 6, Arbitrary cleaning apparatuses, such as a brush cleaner, a magnetic brush cleaner, an electrostatic brush cleaner, a magnetic roller cleaner, a blade cleaner, can be used. The cleaning device 6 is for scraping off residual toner adhering to the photoreceptor 1 with a cleaning member and collecting the residual toner. However, when there is little or almost no toner remaining on the surface of the photoreceptor, the cleaning device 6 may not be provided.

  The fixing device 7 includes an upper fixing member (fixing roller) 71 and a lower fixing member (fixing roller) 72, and a heating device 73 is provided inside the fixing member 71 or 72. FIG. 1 shows an example in which a heating device 73 is provided inside the upper fixing member 71. For the upper and lower fixing members 71 and 72, a known heat fixing member such as a fixing roll in which a metal base tube made of stainless steel, aluminum or the like is coated with silicone rubber, a fixing roll coated with a fluororesin, or a fixing sheet is used. can do. Further, each of the fixing members 71 and 72 may be configured to supply a release agent such as silicone oil in order to improve releasability, or may be configured to forcibly apply pressure to each other by a spring or the like.

  When the toner transferred onto the recording paper P passes between the upper fixing member 71 and the lower fixing member 72 heated to a predetermined temperature, the toner is heated to a molten state and cooled after passing through the recording paper. Toner is fixed on P. The type of the fixing device is not particularly limited, and a fixing device of an arbitrary method such as heat roller fixing, flash fixing, oven fixing, pressure fixing, or the like can be provided.

<Image forming method>
In the electrophotographic apparatus configured as described above, an image is recorded as follows. That is, first, the surface (photosensitive surface) of the photoreceptor 1 is charged to a predetermined potential (for example, −600 V) by the charging device 2. At this time, charging may be performed with a DC voltage, or charging may be performed by superimposing an AC voltage on the DC voltage.

  Subsequently, the photosensitive surface of the charged photoreceptor 1 is exposed by the exposure device 3 according to the image to be recorded, and an electrostatic latent image is formed on the photosensitive surface. The developing device 4 develops the electrostatic latent image formed on the photosensitive surface of the photoreceptor 1.

  The developing device 4 thins the toner T supplied by the supply roller 43 with a regulating member (developing blade) 45 and has a predetermined polarity (here, the same polarity as the charging potential of the photosensitive member 1) and the negative polarity. ), And conveyed while being carried on the developing roller 44 to be brought into contact with the surface of the photoreceptor 1.

  When the charged toner T carried on the developing roller 44 comes into contact with the surface of the photoreceptor 1, a toner image corresponding to the electrostatic latent image is formed on the photosensitive surface of the photoreceptor 1. This toner image is transferred onto the recording paper P by the transfer device 5. Thereafter, the toner remaining on the photosensitive surface of the photoreceptor 1 without being transferred is removed by the cleaning device 6.

  After the transfer of the toner image onto the recording paper P, the final image is obtained by passing the fixing device 7 and thermally fixing the toner image onto the recording paper P. In addition to the above-described configuration, the image forming apparatus may be configured to perform, for example, a static elimination process. The neutralization step is a step of neutralizing the electrophotographic photosensitive member by exposing the electrophotographic photosensitive member, and a fluorescent lamp, an LED, or the like is used as the neutralizing device. In addition, the light used in the static elimination process is often light having an exposure energy that is at least three times that of the exposure light.

  The image forming apparatus may be further modified. For example, the image forming apparatus may be configured to perform a pre-exposure process, an auxiliary charging process, or the like, or may be configured to perform offset printing. A full-color tandem system configuration using toner may be used.

  Hereinafter, the present invention will be described in more detail with reference to production examples, examples and comparative examples. In addition, the following examples are shown in order to explain the present invention in detail, and the present invention is not limited to the following examples unless it is contrary to the gist thereof.

<Manufacture of coating liquid>
(Production Example 1)
100 parts by mass of a polyester resin represented by the following repeating structure (resin 1, viscosity average molecular weight 40,000), 50 parts by mass of a compound (CTM1) represented by the following formula as a charge transport material, and the following formula as an antioxidant 8 parts by mass of the compound represented by formula (AOX1), 0.1 parts by mass of the exemplified compound 2 shown in Table 1, and 0.05 parts by mass of silicone oil as a leveling agent are tetrahydrofuran / toluene (8/2 (mass ratio)). ) A charge transport layer forming coating solution was prepared by dissolving in 640 parts by mass of the mixed solvent. Here, the tetrahydrofuran / toluene mixed solvent had a water content of 1% by mass.

The physical property values of the polyester resin were as follows.
Terminal carboxylic acid group content: 15 μeq / g
Terminal OH group content: 10 μeq / g
Terminal acid chloride group amount: 0.010 μeq / g

(Production Example 2)
A charge transport layer forming coating solution was prepared in the same manner as in Production Example 1 except that 1 part by mass of the exemplified compound 2 used in the charge transport layer forming coating solution of Production Example 1 was used.

(Production Example 3)
The charge transport layer was formed in the same manner as in Production Example 1 except that 0.1 parts by mass of the exemplified compound 11 shown in Table 1 was used instead of the exemplified compound 2 used in the charge transport layer forming coating solution of Production Example 1. A coating solution was prepared.

(Production Example 4)
Coating for charge transport layer formation in the same manner as in Production Example 1 except that 1 part by mass of the exemplified compound 11 shown in Table 1 was used instead of the exemplified compound 2 used in the coating liquid for forming the charge transport layer of Production Example 1. A liquid was prepared.

(Production Example 5)
The charge transport layer was formed in the same manner as in Production Example 1 except that 0.31 part by mass of the exemplified compound 10 shown in Table 1 was used instead of the exemplified compound 2 used in the charge transport layer forming coating solution of Production Example 1. A coating solution was prepared.

(Production Example 6)
The charge transport layer was formed in the same manner as in Production Example 1 except that 0.28 parts by mass of the exemplified compound 17 shown in Table 2 was used instead of the exemplified compound 2 used in the charge transport layer forming coating solution of Production Example 1. A coating solution was prepared.

(Production Example 7)
The charge transport layer was formed in the same manner as in Production Example 1 except that 0.31 part by mass of the exemplified compound 15 shown in Table 2 was used instead of the exemplified compound 2 used in the coating liquid for forming the charge transport layer in Production Example 1. A coating solution was prepared.

(Production Example 8)
The charge transport layer was formed in the same manner as in Production Example 1 except that 0.22 parts by mass of the exemplified compound 16 shown in Table 2 was used instead of the exemplified compound 2 used in the charge transport layer forming coating solution of Production Example 1. A coating solution was prepared.

(Production Example 9)
In the same manner as in Production Example 1 except that 0.35 parts by mass of epoxidized soybean oil O-130P manufactured by Adeka Co., Ltd. was used instead of the exemplified compound 2 used in the coating liquid for forming the charge transport layer of Production Example 1. A coating solution for transport layer formation was prepared.

(Production Example 10)
In the same manner as in Production Example 1 except that 0.26 parts by mass of epoxidized linseed oil O-180A manufactured by Adeka Co., Ltd. was used instead of the exemplified compound 2 used in the coating liquid for forming the charge transport layer of Production Example 1. A coating solution for transport layer formation was prepared.

(Production Example 11)
In the same manner as in Production Example 1 except that 0.56 parts by mass of epoxidized fatty acid octyl ester D-32 manufactured by Adeka Co., Ltd. was used instead of Exemplified Compound 2 used in the coating liquid for forming a charge transport layer in Production Example 1. A coating solution for forming a charge transport layer was prepared.

(Production Example 12)
In the same manner as in Production Example 1 except that 0.50 parts by mass of epoxidized fatty acid alkyl ester D-55 manufactured by Adeka Co., Ltd. was used instead of Exemplified Compound 2 used in the coating liquid for forming the charge transport layer in Production Example 1. A coating solution for forming a charge transport layer was prepared.

(Production Example 13)
The polyester resin (resin 2, viscosity average molecular weight 40,000) represented by the following repeating structure was used in place of the polyester resin (resin 1) used in the charge transport layer forming coating solution of Production Example 5. In the same manner as in Production Example 5, a coating solution for forming a charge transport layer was prepared.

ポリエステル樹脂の物性値は以下の通りであった。
末端カルボン酸基量：１１μｅｑ／ｇ
末端ＯＨ基量：４μｅｑ／ｇ
末端酸クロライド基量：０．０１０μｅｑ／ｇ

The physical property values of the polyester resin were as follows.
Terminal carboxylic acid group amount: 11 μeq / g
Terminal OH group amount: 4 μeq / g
Terminal acid chloride group amount: 0.010 μeq / g

(Production Example 14)
A polycarbonate resin (resin 3, viscosity average molecular weight 30,000) represented by the following repeating structure was used in place of the polyester resin (resin 1) used in the charge transport layer forming coating solution of Production Example 5. In the same manner as in Production Example 5, a coating solution for forming a charge transport layer was prepared.

(Production Example 15)
Instead of the charge transport material (CTM1) used in the coating liquid for forming the charge transport layer of Production Example 1, a composition (CTM2) described in JP-A-2002-080432, which mainly comprises a structure represented by the following formula, A coating solution for forming a charge transport layer was prepared in the same manner as in Production Example 1 except that Exemplified Compound 2 was changed to 1 part by mass.

(Production Example 16)
Coating for charge transport layer formation in the same manner as in Production Example 15 except that 1 part by mass of the exemplified compound 17 shown in Table 2 was used instead of the exemplified compound 2 used in the coating liquid for forming the charge transport layer of Production Example 15. A liquid was prepared.

(Production Example 17)
The charge transport layer was formed in the same manner as in Production Example 1 except that 0.23 parts by mass of the exemplified compound 5 shown in Table 1 was used instead of the exemplified compound 2 used in the coating liquid for forming the charge transport layer in Production Example 1. A coating solution was prepared.

(Production Example 18)
The charge transport layer was formed in the same manner as in Production Example 1 except that 0.28 parts by mass of the exemplified compound 6 shown in Table 1 was used instead of the exemplified compound 2 used in the coating liquid for forming the charge transport layer in Production Example 1. A coating solution was prepared.

(Production Example 19)
The charge transport layer was formed in the same manner as in Production Example 1 except that 0.32 parts by mass of the exemplified compound 7 shown in Table 1 was used instead of the exemplified compound 2 used in the charge transport layer forming coating solution of Production Example 1. A coating solution was prepared.

(Production Example 20)
The charge transport layer was formed in the same manner as in Production Example 1 except that 0.36 parts by mass of the exemplified compound 8 shown in Table 1 was used instead of the exemplified compound 2 used in the charge transport layer forming coating solution of Production Example 1. A coating solution was prepared.

(Production Example 21)
The charge transport layer was formed in the same manner as in Production Example 1 except that 0.40 parts by mass of the exemplified compound 9 shown in Table 1 was used instead of the exemplified compound 2 used in the charge transport layer forming coating solution of Production Example 1. A coating solution was prepared.

(Production Example 22)
A charge transport layer forming coating solution was prepared in the same manner as in Production Example 1 except that Example Compound 2 used in the charge transport layer forming coating solution of Production Example 1 was not used.

(Production Example 23)
A charge transport layer forming coating solution was prepared in the same manner as in Production Example 15 except that Example Compound 2 used in the charge transport layer forming coating solution of Production Example 15 was not used.

<Measurement method of viscosity average molecular weight>
A sample was dissolved in methylene chloride to prepare a solution having a concentration C of 6.00 g / L. The flow time t of the sample solution was measured in a constant temperature water bath set at 20.0 ° C. using an Ubbelohde capillary viscometer with a flow time t ₀ of the solvent (methylene chloride) of 136.21 seconds. The viscosity average molecular weight Mv was calculated according to the following formula.
a = 0.438 × η _sp +1 η _sp = t / t ₀ −1
b = 100 × η _sp / C C = 6.00 (g / L)
η = b / a
Mv = 3207 × η ^1.205

<Method for measuring the amount of terminal carboxylic acid (—COOH) group>
About 0.4 g of polyarylate resin (polyester resin) was precisely weighed in a tall beaker, and 25 mL of benzyl alcohol was added and dissolved by heating in an oil bath at 195 ° C. After confirming complete dissolution, the solution was removed from the oil bath and cooled. After cooling, 2 mL of ethyl alcohol was gently introduced along the wall of the tall beaker.
This solution was titrated with a 0.01N NaOH benzyl alcohol solution using an automatic titrator (GT100, manufactured by Mitsubishi Chemical).
Separately, only the solvent benzyl alcohol was titrated with a 0.01 N NaOH benzyl alcohol solution to obtain a blank value.

Moreover, the factor of 0.01N-NaOH benzyl alcohol liquid was calculated | required with the following method. (1) 10 mL of 0.1 N hydrochloric acid (HCL) (volumetric reagent known defined solution (F _HCL ) was accurately put into a 100 ml volumetric flask with a whole pipette, and the mark was aligned with demineralized water and mixed uniformly.
(2) 1, 2, 4 ml of the preparation solution of (1) was accurately weighed in a tall beaker for titration with a whole pipette.
(3) 25 ml of benzyl alcohol and 2 ml of ethyl alcohol were added to each.
(4) Using an automatic titrator (GT100, manufactured by Mitsubishi Chemical), titration was performed with a 0.01 N NaOH benzyl alcohol solution.
(5) Plot the amount of NaOH benzyl alcohol titrant (Y-axis) against the amount of hydrochloric acid-adjusted solution (X-axis) in calculation (1).
Factor of 0.01N-NaOH benzyl alcohol solution F = F _HCL / S
・ Terminal COOH group = (A−B) × F × 10 / W
Terminal COOH group: equivalent / 10 ⁶ g (= μeq / g)
A: Determination titration (ml)
B: Blank titration (ml)
F: Factor of 0.01N NaOH benzyl alcohol solution W: Polyarylate resin amount (g)

<Measurement method of terminal OH group amount>
About 0.2 g of polyarylate resin (polyester resin) was precisely weighed and dissolved in 10 mL of methylene chloride. To this was added 5 mL of a 5% by mass acetic acid / methylene chloride solution, and further 10 mL of titanium tetrachloride solution (* 1) was added for color development, and then the total liquid volume was adjusted to 25 mL. This solution was measured for absorbance at a wavelength of 480 nm using a spectrophotometer (* 1: mixed solution of 450 mL of methylene chloride, 5 mL of 5% by mass acetic acid / methylene chloride solution, and 12.5 mL of titanium tetrachloride). Separately, the extinction coefficient was determined using a methylene chloride solution of a bisphenol compound (composition) having the same composition as the polyarylate resin to be measured, and the amount of OH groups in the resin was quantified.

<Method for measuring the amount of terminal acid chloride groups>
About 1 g of polyarylate resin (polyester resin) was precisely weighed, and 20 mL of methylene chloride was added and dissolved. To this, 2 mL of a 1% by mass methylene chloride solution of 4- (p-nitrobenzyl) pyridine was added for color development, and then the total liquid volume was adjusted to 25 mL. The absorbance of the solution at a wavelength of 440 nm was measured using a spectrophotometer. Separately, the extinction coefficient was determined using a methylene chloride solution of benzoyl chloride, and the amount of terminal acid chloride groups in the resin was quantified.

<Production of electrophotographic photoreceptor>
Example 1
Rutile type titanium oxide having an average primary particle diameter of 40 nm (“TTO55N” manufactured by Ishihara Sangyo Co., Ltd.) and 3% by mass of methyldimethoxysilane (“TSL8117” manufactured by Toshiba Silicone Co., Ltd.) with respect to the titanium oxide were mixed using a Henschel mixer. The surface-treated titanium oxide obtained by mixing was dispersed by a ball mill in a mixed solvent having a mass ratio of methanol / 1-propanol of 7/3 to obtain a surface-treated titanium oxide dispersed slurry. The dispersion slurry, a mixed solvent of methanol / 1-propanol / toluene, and ε-caprolactam [compound represented by the following formula (A)] / bis (4-amino-3-methylcyclohexyl) methane [the following formula (B ) / Hexamethylenediamine [compound represented by the following formula (C)] / decamethylene dicarboxylic acid [compound represented by the following formula (D)] / octadecamethylene dicarboxylic acid [following formula ( The compound represented by E)] has a composition molar ratio of 60% / 15% / 5% / 15% / 5% and is agitated and mixed with pellets of copolymerized polyamide to dissolve the polyamide pellets. After that, by performing ultrasonic dispersion treatment, the mass ratio of methanol / 1-propanol / toluene is 7/1/2, and the surface-treated titanium oxide / copolymerized polyamide. Containing in a weight ratio 3/1, to prepare a coating liquid for forming an undercoat layer having a solid concentration of 18.0 mass%.

A substrate obtained by depositing aluminum on a 75 μm thick polyester film was used as a support, and the above coating solution for forming the undercoat layer was applied with a wire bar so that the film thickness after drying was 1.3 μm. A pull layer was provided.
Next, as a charge generation material, 20 parts by mass of oxytitanium phthalocyanine and 280 parts by mass of 1,2-dimethoxyethane shown in the X-ray diffraction spectrum of FIG. 2 are mixed, and pulverized and dispersed in a sand grind mill for 1 hour. Processed. Subsequently, 10 parts by mass of polyvinyl butyral (trade name “Denkabutyral” # 6000C, manufactured by Denki Kagaku Kogyo Co., Ltd.) was added to 255 parts by mass of 1,2-dimethoxyethane and 4-methoxy-4-methyl. A binder solution obtained by dissolving in 85 parts by mass of 2-pentanone and 230 parts by mass of 1,2-dimethoxyethane were mixed to prepare a coating solution for forming a charge generation layer. On the film provided with the undercoat layer, the charge generation layer forming coating solution was applied with a wire bar so that the film thickness after drying was 0.4 μm and dried to form a charge generation layer.

Next, the charge transport layer forming coating solution prepared in Production Example 1 is applied onto the charge generation layer with a film applicator so that the film thickness after drying is 25 μm and dried to form a charge transport layer. As a result, an electrophotographic photosensitive member having a laminated photosensitive layer was produced.
Further, the charge transport layer forming coating solution produced in Production Example 1 was accelerated and deteriorated by storing it at a temperature of 55 ° C. for 1 week. An electrophotographic photoreceptor was produced in the same manner using this coating solution.
Each of the electrophotographic photoreceptors prepared using the coating liquid at the initial stage and after the accelerated deterioration was subjected to an electrical property test described later, and the stability of the coating liquid was evaluated by comparison. The results are shown in Table 3. Further, the electrophotographic photosensitive member produced using the initial coating solution was subjected to a wear test which will be described later, and the results are shown in Table 3.

<Electrical characteristics test>
Using an electrophotographic characteristic evaluation apparatus (basic and applied electrophotographic technology, edited by Electrophotographic Society, Corona, pages 404-405) compliant with the electrophotographic society measurement standard, the photosensitive drum is rotated at a constant speed. Then, an electrical property evaluation test was performed by a cycle of charging, exposure, potential measurement, and static elimination. The initial surface potential was -700 V, monochromatic light of 780 nm as exposure light and 660 nm as charge removal light, and the surface potential (VL) when exposure light was irradiated at 1.0 μJ / cm ² was measured. In the VL measurement, the time required from the exposure to the potential measurement was 100 ms. The measurement environment was a temperature of 25 ° C. and a relative humidity of 50% (NN environment). The smaller the absolute value of the VL value, the better the response (unit: -V). The results are shown in Table 1.

<Abrasion test>
The photoreceptor sheet was cut into a circle having a diameter of 10 cm, and the wear was evaluated by a Taber abrasion tester (manufactured by Taber). The test conditions were measured by comparing the mass before and after the test with 1000 wheels with no load (the weight of the wear wheel) under the atmosphere of 23 ° C. and 50% RH without load (self-weight of the wear wheel). did.

(Examples 2 to 21)
The same procedure as in Example 1 was used except that the charge transport layer forming coating solution prepared in Preparation Examples 2 to 21 was used instead of the charge transport layer forming coating solution prepared in Manufacturing Example 1 used in Example 1. An electrophotographic photoreceptor was prepared and evaluated. The results are shown in Table 3.

(Comparative Examples 1-2)
In the same manner as in Example 1, except that the charge transport layer forming coating solution prepared in Production Examples 22 to 23 was used instead of the charge transport layer forming coating solution prepared in Production Example 1 used in Example 1. An electrophotographic photoreceptor was prepared and evaluated. The results are shown in Table 3.

As shown in Examples 1 to 21, by adding an epoxy group-containing compound, there was little change with time and stable electrical characteristics were exhibited. In addition, the increase in the initial VL due to the addition of the epoxy group-containing compound was slight. In particular, when a polyarylate resin is used, particularly when an enamine compound is used in combination, the inhibitory effect due to the addition is noticeable.
In the formula (A), a resin in which Y is an oxygen atom has excellent wear resistance and can provide a high-performance photoconductor.

(Example 22)
The surface of an aluminum cylinder having a mirror-finished outer diameter of 30 mm, length of 376 mm, and wall thickness of 0.75 mm is anodized and then sealed with a sealant mainly composed of nickel acetate. By performing, an anodic oxide film (alumite film) of about 6 μm was formed. The charge generation layer forming coating solution prepared in Example 1 and the charge transport layer forming coating solution prepared in Example 5 are sequentially dip coated on this cylinder, and the film thickness after drying becomes 0.4 μm and 18 μm, respectively. Thus, a charge generation layer and a charge transport layer were formed to obtain an electrophotographic photosensitive drum.

  The produced photosensitive drum was mounted on a black drum cartridge for a color printer MICROLINE Pro 9800PS-E manufactured by Oki Data. Next, a developing toner (volume average particle diameter 7.05 μm, Dv / Dn = 1.14, average circularity 0.963) manufactured according to the manufacturing method of developing toner A disclosed in Japanese Patent Application Laid-Open No. 2007-213050 is black. Mounted on a toner cartridge. These drum cartridges and toner cartridges were mounted on the printer.

Specifications of MICROLINE Pro 9800PS-E 4 tandem color 36ppm, monochrome 40ppm
1200 dpi
Contact roller charging (DC voltage applied)
LED exposure With static elimination light Initial and 30,000 images were formed in an environment with a temperature of 25 ° C and a humidity of 50%, and in all cases, a good image with no image degradation such as ghosting, fogging, and density reduction was obtained. It was.

(Example 23)
A cylinder made of an aluminum alloy having an outer diameter of 30 mm, a length of 254 mm, and a wall thickness of 0.75 mm whose surface has been roughly cut (Rmax = 0.8) is dip-coated in the coating solution for forming the undercoat layer produced in Example 1. An undercoat layer having a thickness of about 1.3 μm was formed. The cylinder is formed by dip-coating the coating solution for forming the charge generation layer prepared in Example 1 and the coating solution for forming the charge transport layer prepared in Example 5 in order, and the film thickness after drying becomes 0.3 μm and 25 μm, respectively. Thus, a charge generation layer and a charge transport layer were formed to obtain an electrophotographic photosensitive drum.

  This photoconductor is mounted on a commercially available monochrome laser printer (manufactured by Lexmark, Optra S2450, 24 sheets per minute at A4 vertical feed, DC charging roller charging, roller transfer) and 30,000 sheets at room temperature and humidity. Printed out. A good image with no image deterioration such as ghost, fogging and density reduction was obtained both at the initial stage and after the 30,000-sheet image formation.

(Example 24)
The surface of a cylinder made of an aluminum alloy having an outer diameter of 30 mm, a length of 346 mm, and a wall thickness of 1.0 mm, whose surface has been roughly cut (Rmax = 1.0), is subjected to anodizing treatment, and then nickel acetate as a main component. By performing sealing treatment with a sealing agent, an anodic oxide coating (alumite coating) of about 6 μm was formed.
This cylinder was dip-coated in the undercoat layer-forming coating solution prepared in Example 1 to form an undercoat layer having a thickness of about 1.3 μm after drying. The cylinder is formed by dip-coating the coating solution for forming the charge generation layer prepared in Example 1 and the coating solution for forming the charge transport layer prepared in Example 5 in order, and the film thickness after drying becomes 0.3 μm and 25 μm, respectively. Thus, a charge generation layer and a charge transport layer were formed to obtain an electrophotographic photosensitive drum.

This photosensitive drum is mounted on a commercially available digital multifunction machine (manufactured by Panasonic Communications Co., Ltd., WORKIO3200, A4 horizontal feed 32 sheets / minute, roller charging with AC superimposed DC voltage applied, magnetic one component jumping development, resolution 600 dpi × 600 dpi). 30,000 sheets were printed under normal temperature and humidity.
A good image with no image deterioration such as ghost, fogging and density reduction was obtained both at the initial stage and after the 30,000-sheet image formation.

  Although the present invention has been described with reference to the most practical and preferred embodiments at the present time, the invention is limited to the embodiments disclosed herein. However, it can be changed as appropriate without departing from the spirit or concept of the invention that can be read from the claims and the entire specification, and the coating liquid for producing an electrophotographic photosensitive member, the electrophotographic photosensitive member, and image formation accompanying such a change. Devices and electrophotographic photoreceptor cartridges should also be understood as being within the scope of the present invention.

  The present invention can be carried out in any field that requires an electrophotographic photoreceptor, and is suitable for use in, for example, a copying machine, a printer, a printing machine, and the like.

1 is a schematic diagram illustrating a main configuration of an embodiment of an image forming apparatus of the present invention. X-ray analysis spectrum of oxytitanium phthalocyanine used in Example 1

Explanation of symbols

1 Photoconductor (Electrophotographic photoconductor)
2 Charging device (charging roller; charging unit)
3 Exposure equipment (exposure section)
4 Development device (development unit)
DESCRIPTION OF SYMBOLS 5 Transfer apparatus 6 Cleaning apparatus 7 Fixing apparatus 41 Developing tank 42 Agitator 43 Supply roller 44 Developing roller 45 Control member 71 Upper fixing member (fixing roller)
72 Lower fixing member (fixing roller)
73 Heating device T Toner P Recording paper (paper, medium)

Claims (12)

A coating solution for producing an electrophotographic photoreceptor comprising an enamine compound as a charge transport material,
A coating solution for producing an electrophotographic photosensitive member, comprising a non-nitrogen acid scavenger. The coating solution for producing an electrophotographic photosensitive member according to claim 1, wherein the non-nitrogen acid scavenger is an epoxy group-containing compound. The coating solution for producing an electrophotographic photosensitive member according to claim 1, comprising a polyarylate resin. The coating solution for producing an electrophotographic photosensitive member according to claim 3, wherein the polyarylate resin has a repeating structure represented by the following formula (A).

(In the formula (A), Ar ^{a1 to} Ar ^a4 each independently represent an arylene group which may have a substituent, X and Y each represents a single bond or a divalent group, and k represents 0 or 1 . ) In an electrophotographic photosensitive member having a photosensitive layer on a conductive support, the photosensitive layer comprises:
An enamine compound as a charge transport material ;
A non-nitrogen acid scavenger ;
An electrophotographic photosensitive member comprising: The electrophotographic photosensitive member according to claim 5 , wherein the non-nitrogen acid scavenger is an epoxy group-containing compound. It said photosensitive layer contains a polyarylate resin, electrophotographic photosensitive member according to claim 5 or 6. The electrophotographic photosensitive member according to claim 7 , wherein the polyarylate resin has a repeating structure represented by the following formula (A).

(In the formula (A), Ar ^{a1 to} Ar ^a4 each independently represent an arylene group which may have a substituent, X and Y each represents a single bond or a divalent group, and k represents 0 or 1 . ) 9. The electrophotographic photosensitive member according to claim 5 , charging means for charging the electrophotographic photosensitive member, and image exposing means for forming an electrostatic latent image by performing image exposure on the charged electrophotographic photosensitive member. An image forming apparatus comprising: a developing unit that develops the electrostatic latent image with toner; and a transfer unit that transfers the toner to a transfer target. The image forming apparatus according to claim 9 , wherein the charging unit is a contact charging method. Charging means for charging the electrophotographic photosensitive member, image exposing means for performing image exposure on the charged electrophotographic photosensitive member to form an electrostatic latent image, developing means for developing the electrostatic latent image with toner, and An electrophotographic photosensitive member cartridge comprising: at least one means selected from the group consisting of transfer means for transferring toner to a transfer target; and the electrophotographic photosensitive member according to claim 5 . The electrophotographic photosensitive member cartridge according to claim 11 , wherein the charging unit is a contact charging type.

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