JP5475416B2 - Method for producing electrophotographic photosensitive member - Google Patents

Description

  The present invention relates to a method for producing an electrophotographic photoreceptor.

  As an electrophotographic photosensitive member, a photosensitive layer (organic photosensitive layer) using an organic material as a photoconductive substance (a charge generating substance or a charge transporting substance) is provided on a support due to advantages such as low cost and high productivity. An electrophotographic photoreceptor (so-called organic photoreceptor) is widely used.

  Electrical and mechanical external forces are directly applied to the surface of the electrophotographic photosensitive member by an electrophotographic process such as charging, exposure, toner development, transfer to paper, and cleaning, and thus durability against them is required. Specifically, durability against the occurrence of surface wear and scratches due to rubbing, surface deterioration due to a charging process, and deterioration of electrical characteristics such as sensitivity and charging ability is required. As one of techniques for achieving both durability and high image quality of an output image, a method of providing a protective layer on a photosensitive layer is also known, and this means may be used as necessary.

  Incidentally, since the surface layer of the organic photoreceptor is generally composed of a thin resin layer, the characteristics of the resin used for the surface layer greatly affect the durability of the electrophotographic photoreceptor. A polycarbonate resin is widely used as the resin for the surface layer.

In recent years, the speed of electrophotographic apparatuses has been increased, and further improvement in durability has been demanded. For this reason, a curable resin (or curable material) having a mechanical strength higher than that of a thermoplastic resin such as a polycarbonate resin may be used as the binder resin. In particular, since a protective layer using a curable resin is excellent in wear resistance, it is effective for extending the life of the organic photoreceptor. Here, the curable resin is a resin obtained by curing a monomer or oligomer having a polymerizable functional group that undergoes a polymerization reaction and / or a crosslinking reaction when the polymerizable functional group is cured. That is. As energy given to the monomer or oligomer having a polymerizable functional group, light, heat or radiation energy can be used.
In the case of curing using thermal energy, a method of applying a thermosetting resin to the surface layer has been proposed (see Patent Document 1, Patent Document 2, and Patent Document 3).

  Moreover, as a method of polymerizing by irradiation with radiation, a technique using an electron beam has been proposed (see Patent Document 4). For curing by electron beam irradiation (hereinafter also referred to as “electron beam curing”), a polymerization initiator that may adversely affect the potential characteristics (sensitivity, residual potential, etc.) of the electrophotographic photosensitive member is not used. There is an advantage that it may be. In addition, since it can cause an efficient polymerization reaction in a short time, the productivity is high, and since the electron beam permeability is high, there are shielding substances such as fine particles and additives in the layer containing the curable material. However, there is an advantage that the polymerization reaction and / or the cross-linking reaction are hardly inhibited.

  When a curable resin is used for the surface layer, the amount of wear on the surface of the photoconductor during use is reduced, which is advantageous for extending the life of the photoconductor, but on the other hand, there is a problem that image flow tends to occur. there were. Image flow refers to the electrostatic latent image formed in the exposure process as a result of degradation of the photoreceptor surface due to use and the adhesion of charged products generated in the photoreceptor charging process, resulting in a decrease in the electrical resistance of the photoreceptor surface. This is a phenomenon in which the image is blurred due to disturbance. Deteriorated parts and attached charged products generated on the surface of the photoconductor are removed together with the surface of the photoconductor if it is scraped during printing. In the case of a photoconductor having a surface layer with excellent wear resistance, this wear is removed. It is considered that the image flow tends to occur because the amount is small.

  As a means for suppressing such surface deterioration, a method of adding an additive is known, and a technique for incorporating an antioxidant into a surface layer made of a resin having crosslinkability has been proposed (Patent Document). 5). Moreover, the technique which contains the compound of the specific structure which has an alkylamino group is proposed (refer patent document 6).

JP-A-5-181299 JP 2002-6526 A JP 2002-82465 A JP 2000-066425 A JP 2004-240047 A JP 2007-272192 A

However, when adding an additive for suppressing image flow to a surface layer using a curable resin, it is difficult to select a material that can be used as an additive in the conventional example. This is because it is necessary to select a material that does not adversely affect both the durability and electrical characteristics of the electrophotographic photosensitive member and that has good solubility and dispersibility in the coating material for the surface layer.
The adverse effect on durability means that the addition of an additive inhibits the curing of the surface layer, resulting in a decrease in the wear resistance of the electrophotographic photosensitive member. An adverse effect on electrical characteristics indicates an increase in sensitivity and residual potential due to carrier trapping and an increase in potential fluctuation during continuous printing.

In addition, since additives are added at the stage of creating the surface layer coating material, additives that do not dissolve in the liquid component of the surface layer coating material, or additives that are difficult to disperse uniformly, have good coatability and film formability. It is difficult to use because it causes problems.
An object of the present invention is to provide a method for producing an electrophotographic photoreceptor in which an additive having low solubility and dispersibility in the outermost surface layer coating material is uniformly dispersed in a surface layer using a curable resin.
Another object of the present invention is to provide a method for producing an electrophotographic photoreceptor in which inhibition of curing of a curable material due to the addition of an additive is suppressed.

The present invention is a method for producing an electrophotographic photoreceptor having an outermost surface layer containing a curable resin, the production method comprising the following steps:
(A) a step of preparing a solution by dissolving a substance insoluble in the liquid medium of the coating material for the outermost surface layer containing the curable material in a solvent;
(B) a step of immersing porous particles in the solution obtained in step (A) to obtain porous particles containing the substance;
(C) step said porous particles obtained in (B) is dispersed in the liquid medium preparing a coating the outermost surface layer,
(D) Step step by coating the outermost surface layer coating material obtained in (C) to form a coating film, and step (E) to cure the coating film formed in (D) the outermost layer The present invention relates to a method for producing an electrophotographic photosensitive member characterized by having a forming step.

  According to the present invention, an additive having low solubility and dispersibility in the liquid component of the outermost surface layer coating material containing a curable material is a porous particle having good dispersibility in the liquid component of the outermost surface layer coating material. And the porous particles are dispersed in the outermost surface layer. As a result, the additive can be uniformly distributed in the outermost surface layer in the form of being supported on the porous particles. In addition, it is possible to suppress a decrease in curability of the outermost surface layer compared to when the additive is directly added. As a result, it is difficult to dissolve or disperse in the paint, so that it is possible to use an additive that has been difficult to use in the past.

  Further, by polishing the surface of the outermost surface layer in which the porous particles are dispersed to expose the porous particles existing in the vicinity of the surface, it is possible to further easily exert the effect of suppressing image flow.

It is the schematic of the electrophotographic photoreceptor obtained by the manufacturing method of the electrophotographic photoreceptor of this invention.

また、必用に応じて重合性のモノマーやオリゴマーと組み合わせて用いられる溶剤としては、アルコール、ケトンのような極性溶媒、ヘキサンのような無極性溶媒を挙げることができる。
一般式（Ａ）の化合物と１−プロパノールの混合液に対して不溶である酸化防止剤やアミン化合物の例としては、下記構造式（Ｂ）〜（Ｅ）がある。

第一の工程では、画像流れに対する効果を発揮するのに十分な量の有効物質を、該有効物質が可溶な溶剤に添加して溶解させる。溶剤の種類は該有効物質を可溶なものであれば特に限定されないが、アルコール、ケトンのような極性溶媒、ヘキサンのような無極性溶媒を挙げることができる。ここで選ばれる溶剤は、最表面層用塗料に溶剤が含有される場合、該塗料中の溶剤とは異なるものになる。 Each step included in the method for producing an electrophotographic photosensitive member of the present invention will be described.
First, a process (process (A)) in which a substance insoluble in the liquid component of the paint for the outermost surface layer is dissolved in a solvent in which the substance is soluble will be described (process (A)). In the present invention, the substance is not particularly limited as long as it satisfies the requirement that it is a substance effective for image flow, but a known antioxidant or amine compound can be used. Examples of known antioxidants and amine compounds include alkylamine compounds, diamine compounds, cyclic amine compounds, hindered amine compounds, and hindered phenol compounds. Hereinafter, for simplicity, the substance is also simply referred to as “effective substance”. Further, in the present invention, being insoluble in the liquid component of the paint for the outermost surface layer means that the effective substance is added to the liquid component of the paint in an amount necessary to exert an effect on the image flow. It means that you can melt undissolved. Here, the liquid component of the paint for the outermost surface layer is a mixture of a solvent and a curable material (a monomer or oligomer having a polymerizable functional group) that is liquid at room temperature if the paint contains a solvent. means.
Examples of the monomer or oligomer having a polymerizable functional group include a chain polymerization material having an acryloyloxy group and a styrene group, and a sequential polymerization material having a hydroxyl group, an alkoxysilyl group, and an isocyanate group. From the viewpoints of electrophotographic characteristics, versatility, material design, and production stability, chain polymerization materials are preferred.
In addition, a polymerizable monomer or oligomer having a charge transporting group may be used as the polymerizable monomer or oligomer, and among them, a monomer or oligomer having a hole transporting group and an acryloyloxy group in the same molecule may be used. preferable. As an example, the compound of the following general formula (A) can be mentioned.

Moreover, as a solvent used in combination with a polymerizable monomer or oligomer as necessary, there can be mentioned a polar solvent such as alcohol and ketone, and a nonpolar solvent such as hexane.
Examples of antioxidants and amine compounds that are insoluble in the mixture of the compound of general formula (A) and 1-propanol include the following structural formulas (B) to (E).

In the first step, a sufficient amount of an effective substance for exhibiting an effect on image flow is added to a solvent in which the effective substance is soluble and dissolved. The type of the solvent is not particularly limited as long as the effective substance is soluble, and examples thereof include polar solvents such as alcohol and ketone, and nonpolar solvents such as hexane. The solvent selected here is different from the solvent in the paint when the outermost surface layer paint contains a solvent.

  Secondly, a step (step (B)) in which porous particles are immersed in the solution obtained in the first step to produce porous particles containing an effective substance will be described. In this step, the porous particles are immersed in the solution, and the porous particles are soaked with the solution. Next, the porous particles containing the active substance are obtained by filtering and / or drying the solvent. As the porous particles, known porous particles such as porous silica and hollow particles can be used as long as they are insoluble in the liquid component of the solution and the coating material. However, since it is necessary to disperse the porous particles in the coating for the outermost surface layer in a later step, it is preferable that the porous particles have excellent dispersibility. In addition, it is more preferable if the particles can carry more active substances. Hollow particles made of a styrene-acrylic copolymer resin are excellent in ability to support an effective substance and dispersibility in a paint, and can be preferably used.

  Thirdly, the step (step (C)) of making the outermost surface layer coating material by dispersing the porous particles containing the active substance obtained in the second step in the liquid component of the outermost surface layer coating material will be described. . As a method of dispersing the porous particles obtained in the second step in the coating for the outermost surface layer, known dispersion such as a homogenizer, ultrasonic dispersion, ball mill, vibration ball mill, sand mill, attritor, roll mill or high pressure disperser The method can be used. In addition to the curable resin and the porous particles, a functional material such as a charge transporting substance and a lubricant such as polytetrafluoroethylene particles may be added to the outermost surface layer coating material as necessary.

  Fourth, the step (step (D)) of forming the coating film by applying the coating for the outermost surface layer obtained in the third step will be described. Examples of the method for forming the coating film include methods such as coating using a bar coater, knife coater, and roll coater, dip coating, spray coating, and beam coating.

  Fifth, the step (step (E)) of forming the outermost surface layer of the electrophotographic photosensitive member by curing the coating film formed in the fourth step will be described. In the present invention, since the curable material is contained in the coating for the outermost layer, energy is applied by heat, light, or radiation to cure the curable material. As the heating means, a hot air drying furnace, a high-frequency electromagnetic induction heating means, or the like can be used. In the case of curing by light irradiation, means such as an ultraviolet lamp can be used. Here, examples of the lamp include a low pressure mercury lamp such as a fluorescent chemical lamp, a high pressure discharge lamp such as a high pressure mercury lamp and a metal halide lamp, and a short arc discharge lamp such as a xenon lamp. Moreover, when using a radiation, an electron beam can be used preferably especially.

The case where an electron beam is used will be described in more detail. Examples of the accelerator used for electron beam irradiation include accelerators such as a scanning type, an electro curtain type, a broad beam type, a pulse type, and a laminar type. The acceleration voltage of the electron beam is preferably in the range of 70 to 250 kV, and more preferably in the range of 70 to 150 kV. The absorbed dose of the electron beam is preferably in the range of 9 × 10 ³ to 1 × 10 ⁶ Gy, and more preferably in the range of 9 × 10 ^{3 to} 5 × 10 ⁵ Gy.

  If the accelerating voltage is too large, the potential characteristics of the electrophotographic photosensitive member due to electron beam irradiation tend to deteriorate significantly. On the other hand, if the acceleration voltage is too small, the surface layer may be insufficiently polymerized and cured. If the absorbed dose is too small, the surface layer may be insufficiently polymerized and cured. When the absorbed dose is too large, the potential characteristics of the electrophotographic photosensitive member tend to deteriorate significantly.

The absorbed dose of the electron beam can be measured by a general-purpose film dosimeter (for example, a RADIA CHROMIC READER and a Radiological dosimeter (10 μm) manufactured by Far West Technology). However, the absorbed dose that can be directly measured is 1 × 10 ⁵ Gy or less, and if it is more than that, it is estimated from the current value (or time) when the absorbed dose of 1 × 10 ⁵ Gy or less is measured.

  Further, the absorbed dose of the electron beam in the present invention is an absorbed dose of the electron beam on the surface of the irradiated object. Then, the radiation dose measured when the film of the above-mentioned Radiachromic dosimeter (10 μm) is attached to the surface of the irradiated object before the surface layer coating solution is applied, and the electron beam is irradiated in that state. means.

  As described above, there are a plurality of means for curing the curable material, but these curing means may be used alone or in combination of a plurality of means.

  By producing an electrophotographic photosensitive member through the above-mentioned processes, a material effective for image flow that is difficult to add directly to the outermost surface layer is uniformly applied to the outermost surface layer in the form of being supported on porous particles. Can be dispersed. Further, with the use of the electrophotographic photosensitive member, the porous particles are exposed on the surface of the photosensitive member, and are gradually scraped off, whereby an effect on image flow can be continuously obtained. Even when an unused photoreceptor is used, the surface thereof is polished and roughened in advance, so that the porous particles are exposed on the photoreceptor surface, and a part thereof can be scraped off. That is, by adding the process of roughening the surface of the photoconductor, the effect of suppressing image flow immediately after the start of use of the photoconductor can be further enhanced.

  In addition, if the added amount is large, an effective substance such as an antioxidant that may cause curing inhibition of the curable material is supported on the porous substance, so that such an adverse effect can be suppressed. Although the details of this mechanism are unknown, it is presumed that the effective substance is supported on the porous particles and the mixing of the curable material and the effective substance is suppressed, and as a result, the inhibition of curing is less likely to occur.

As a method for evaluating the degree of curing of the curable material, there is a method for evaluating the degree of remaining uncured functional groups on the surface of the photoreceptor after curing. In the case of an acryloyloxy group as the uncured functional group, a terminal olefin (CH ₂ =) is exemplified. In order to evaluate the remaining amount of the terminal olefin (CH ₂ =), a method of using infrared spectroscopic reflection method using a fragment of the photoreceptor surface layer as a sample can be mentioned. In the infrared spectral reflection method, the peak area ratio may be calculated using the peak area of the terminal olefin (CH ₂ =) of the acryloyloxy group as the numerator and the peak area of the carbonyl (C═O) of the acryloyloxy group as the denominator. (Hereinafter, this peak area ratio is called uncured residual group IR peak ratio). Since the peak wave number in the infrared spectrum is affected by the molecular structure and curing, it often differs depending on the curable material. For example, in the case of a cured arylamine compound having an acryloyloxy group, a peak based on the carbonyl (C═O) stretching vibration of the acryloyloxy group is seen in the vicinity of 1725 cm ⁻¹ , and the terminal olefin (CH ₂ =) plane A peak based on the internal bending vibration is seen in the vicinity of 1405 cm ⁻¹ .

  FIG. 1 shows a schematic diagram of a typical example of an electrophotographic photoreceptor produced by the method for producing an electrophotographic photoreceptor of the present invention. In this electrophotographic photosensitive member, a conductive layer 2, an intermediate layer 3, a charge generation layer 4, a charge transport layer 5, and a second charge transport layer as an outermost surface layer 6 are arranged in this order on the conductive support 1. Is formed. In the second charge transport layer as the outermost surface layer, porous particles 7 containing an effective substance are uniformly dispersed.

Next, the structure of the electrophotographic photoreceptor produced by the production method of the present invention will be specifically described.
As the electrophotographic photosensitive member, a cylindrical photosensitive member in which a charge generation layer and a charge transport layer are provided on a cylindrical support is common, but a belt-like or sheet-like one can also be used.

  The support may be anything that exhibits conductivity (conductive support), and examples of the material include iron, copper, gold, silver, aluminum, zinc, titanium, lead, nickel, tin, antimony, and indium. , Metals and alloys such as chromium, aluminum alloy, and stainless steel. A metal support or a plastic support having a layer formed by vacuum deposition of aluminum, an aluminum alloy, or an indium oxide-tin oxide alloy can also be used. Also, a support made by impregnating plastic or paper with conductive binders such as carbon black, tin oxide particles, titanium oxide particles and silver particles together with an appropriate binder resin, or plastic made using conductive binder resin. These supports can also be used.

  The surface of the support may be subjected to cutting treatment, roughening treatment, and alumite treatment for the purpose of preventing interference fringes due to scattering of laser light.

  Further, a conductive layer may be formed between the support and an intermediate layer or charge generation layer, which will be described later, for the purpose of preventing interference fringes due to scattering of laser light and covering the scratches on the support.

  The conductive layer can be formed using a conductive layer coating liquid obtained by dispersing and / or dissolving carbon black, a conductive pigment or a resistance adjusting pigment in a solvent together with a binder resin. The conductive layer coating liquid may contain a compound (polymerizable compound) that is polymerized by heating or radiation irradiation to become a cured product. The surface of a conductive layer containing a conductive pigment or a resistance adjusting pigment tends to be roughened.

  The thickness of the conductive layer is preferably 0.2 to 40 μm, more preferably 1 to 35 μm, and still more preferably 5 to 35 μm.

  Examples of the binder resin used for the conductive layer include polymers / copolymers of vinyl compounds such as styrene, vinyl acetate, vinyl chloride, acrylic acid ester, methacrylic acid ester, vinylidene fluoride, and trifluoroethylene, polyvinyl Examples include alcohol, polyvinyl acetal, polycarbonate, polyester, polysulfone, polyphenylene oxide, polyurethane, cellulose resin, phenol resin, melamine resin, silicon resin, and epoxy resin.

  Examples of conductive pigments and resistance control pigments used in the conductive layer include metal and alloy particles such as aluminum, zinc, copper, chromium, nickel, silver, and stainless steel, and these are deposited on the surface of resin particles. Things. Alternatively, particles of metal oxide such as zinc oxide, titanium oxide, tin oxide, antimony oxide, indium oxide, bismuth oxide, tin-doped indium oxide, antimony or tantalum-doped tin oxide may be used. These particles may be used alone or in combination of two or more. When two or more types are used in combination, they may be simply mixed, or may be in the form of a solid solution or fusion.

  An intermediate layer having a barrier function or an adhesive function may be formed between the support or the conductive layer and the charge generation layer. The intermediate layer is formed to improve the adhesion of the photosensitive layer, improve the coating property, improve the charge injection property from the support, and protect the photosensitive layer from electrical breakdown.

  Examples of the material for the intermediate layer include polyvinyl alcohol, poly-N-vinylimidazole, polyethylene oxide, ethyl cellulose, ethylene-acrylic acid copolymer, casein, polyamide, N-methoxymethylated 6 nylon, copolymer nylon, glue, Examples include gelatin.

The intermediate layer can be formed by applying an intermediate layer coating solution obtained by dissolving the above-described materials in a solvent and drying it.
The layer thickness of the intermediate layer is preferably 0.05 to 7 μm, and more preferably 0.1 to 5 μm.

A charge generation layer is formed on the support, conductive layer or intermediate layer.
Examples of the charge generation material used in the charge generation layer include pyrylium, thiapyrylium dyes, various central metals, and various crystal systems (α, β, γ, ε, X type, etc.) phthalocyanine pigments and anthanthrone pigments. Azo pigments such as dibenzpyrenequinone pigment, pyranthrone pigment, monoazo, disazo and trisazo, indigo pigment, quinacridone pigment, asymmetric quinocyanine pigment and quinocyanine pigment. Further, it may be amorphous silicon. These charge generation materials may be used alone or in combination of two or more.

  Examples of the method for forming the charge generation layer include a method of applying and drying a charge generation layer coating solution, and a method of forming a vapor generation film of a charge generation material.

  The coating solution for the charge generation layer is a homogenizer, ultrasonic dispersion, ball mill, vibration ball mill, sand mill, attritor, roll mill or high pressure, together with a binder resin and a solvent in an amount of 0.3 to 4 times (mass ratio). The dispersion can be obtained by a method using a disperser. Examples of the binder resin include polymers and copolymers of vinyl compounds such as styrene, vinyl acetate, vinyl chloride, acrylic acid ester, methacrylic acid ester, vinylidene fluoride, and trifluoroethylene. Further, polyvinyl alcohol, polyvinyl acetal, polycarbonate, polyester, polysulfone, polyphenylene oxide, polyurethane, cellulose resin, phenol resin, melamine resin, silicon resin, and epoxy resin can be used.

  The thickness of the charge generation layer is preferably 5 μm or less, and more preferably 0.1 to 2 μm.

  A charge transport layer is formed on the charge generation layer. In the present invention, when the charge transport layer is the outermost surface layer, a curable resin is contained as a binder resin. Therefore, in the coating for the charge transport layer, the curable material is described in the description of the step (A). Polymerizable or crosslinkable monomers and oligomers are contained.

  When the outermost surface layer is formed on the charge transport layer, the charge transport layer does not necessarily contain the curable resin. In that case, the same resin as the binder resin for the charge generation layer may be used. Can be used.

  The charge transport layer contains a charge transport material except when the binder resin itself contained therein has a charge transport capability. Examples of the charge transport material used in the charge transport layer include poly-N-vinylcarbazole, a polymer compound having a heterocyclic ring or a condensed polycyclic aromatic compound such as polystyrylanthracene, pyrazoline, imidazole, oxazole, triazole, Low molecular weight compounds such as heterocyclic compounds such as carbazole, triarylalkane derivatives such as triphenylmethane, triarylamine derivatives such as triphenylamine, phenylenediamine derivatives, N-phenylcarbazole derivatives, stilbene derivatives, hydrazone derivatives Compounds.

  The charge transport layer can be formed by applying and drying a charge transport layer coating solution obtained by dissolving a charge transport material and a binder resin in a solvent on the charge generation layer. In the present invention, when the charge transport layer is the outermost surface layer, the amount of the charge transport material contained in the charge transport layer is preferably 20 to 70% by mass, and more preferably 30 to 50% by mass. . However, when the curable resin itself has a charge transporting ability, the amount of the other charge transporting substance added may be 0 to 50% by mass. Moreover, when forming the outermost surface layer containing curable resin on a charge transport layer, it is preferable that the quantity of the charge transport material contained in a charge transport layer is 30-100 mass%, 50-100 More preferably, it is mass%.

  The thickness of the charge transport layer is preferably 5 μm or more and 50 μm or less, and more preferably 8 μm or more and 35 μm or less.

  In the present invention, an outermost surface layer containing a curable resin is provided on the charge transport layer as necessary. The outermost surface layer may be a protective layer because the main purpose is to protect the surface of the photoreceptor, but a layer having a charge transporting capability can be considered as a second charge transporting layer. Here, the second charge transport layer will be described.

  Examples of the charge transport material used in the second charge transport layer include the same materials as those exemplified as the charge transport material used in the charge transport layer (first charge transport layer). As the curable resin contained in the second charge transport layer, the polymerizable or crosslinkable monomer or oligomer described in the description of the step (A) can be used.

  When the curable resin used for the second charge transporting layer has a charge transporting ability, the charge transporting material is not necessarily contained. When the charge transport material is contained, the amount added in the second charge transport layer is preferably 10 to 50% by mass.

  The layer thickness of the second charge transport layer is preferably 0.1 to 20 μm, and more preferably 1 to 10 μm.

  In the present invention, the porous layer is formed by the above-described method with respect to the second charge transport layer serving as the outermost surface layer, or the first charge transport layer serving as the outermost surface layer when the second charge transport layer is not provided. The particles are dispersed and the outermost surface layer is cured to obtain an electrophotographic photosensitive member. Furthermore, you may roughen the surface as needed. As a roughening treatment method, a known method such as a lapping method in which a photosensitive member is rubbed against a polishing sheet containing abrasive grains and polished, or a sand blast method can be used.

  Various additives can be added to each layer of the electrophotographic photoreceptor produced by the production method of the present invention. Examples of the additive include a degradation inhibitor such as an antioxidant and an ultraviolet absorber, and a lubricant such as fluorine atom-containing resin particles.

  The conductive layer, intermediate layer, charge generation layer, and charge transport layer can be applied by, for example, coating using a bar coater, knife coater, or roll coater, dip coating, spray coating, beam coating, electrostatic coating, A method such as particle coating may be mentioned.

  Hereinafter, the present invention will be described in more detail with reference to specific examples. However, the present invention is not limited to these. In the examples, “part” means “part by mass”.

[Example 1]
<Creation of electrophotographic photoreceptor>
An aluminum cylinder having an outer diameter of 30 mm and a length of 370 mm was used as a support (cylindrical support).
Powder made of barium sulfate particles having a tin oxide coating layer (trade name: Pastoran PC1, manufactured by Mitsui Mining & Smelting Co., Ltd.) 60 parts Titanium oxide (trade name: TITANIX JR, manufactured by Teika Co., Ltd.) 15 parts Resol type Phenol resin (trade name: Phenolite J-325, manufactured by Dainippon Ink & Chemicals, Inc., solid content 70%) 43 parts 2-methoxy-1-propanol 50 parts Methanol 50 parts Next, a solution comprising the above materials Was dispersed in a sand mill using glass beads having a diameter of 1 mm for 3 hours to prepare a dispersion.

Silicone resin (trade name: Tospearl 120, manufactured by Momentive Performance Materials Japan LLC) 3.6 parts Silicone oil (trade name: SH28PA, manufactured by Toray Silicone Co., Ltd.) 0.015 parts Next, the above materials Was added to this dispersion and stirred to prepare a coating solution for a conductive layer.
This conductive layer coating solution was dip-coated on a support and heated and cured in an oven at a temperature of 140 ° C. for 1 hour to form a conductive layer having a layer thickness of 15 μm.

Copolymer nylon resin (trade name: Amilan CM8000, manufactured by Toray Industries, Inc.) 10 parts Methoxymethylated 6 nylon resin (trade name: Toresin EF-30T, manufactured by Teikoku Chemical Co., Ltd.)
30 parts Next, the above material was dissolved in a mixed solvent of 400 parts of methanol / 200 parts of n-butanol to prepare a coating solution for an intermediate layer.
This intermediate layer coating solution was dip-coated on the conductive layer and dried (heat-dried) in an oven at a temperature of 100 ° C. for 30 minutes to form an intermediate layer having a layer thickness of 0.4 μm.

ポリビニルブチラール（商品名：エスレックＢＸ−１、積水化学製） １０部
シクロヘキサノン ６００部
次に、上記の材料に、直径１ｍｍのガラスビーズを用いたサンドミル装置で４時間分散処理を施し、その後酢酸エチル７００部を加えて電荷発生層用分散液を調製した。
この電荷発生層用塗布液を中間層上に浸漬塗布し、１０分間温度８５℃のオーブンで乾燥（加熱乾燥）させることにより、層厚が０．１５μｍの電荷発生層を形成した。 Hydroxygallium phthalocyanine (having strong peaks at 7.4 ° and 28.2 ° (Bragg angle 2θ ± 0.2 °) in CuKα characteristic X-ray diffraction)) 20 parts Calix represented by the following structural formula (1) Arene compound 0.2 parts

Polyvinyl butyral (trade name: ESREC BX-1, manufactured by Sekisui Chemical Co., Ltd.) 10 parts Cyclohexanone 600 parts Next, the above material was subjected to a dispersion treatment for 4 hours in a sand mill using glass beads having a diameter of 1 mm, and then ethyl acetate 700 Part was added to prepare a dispersion for charge generation layer.
This charge generation layer coating solution was dip-coated on the intermediate layer and dried (heat-dried) in an oven at a temperature of 85 ° C. for 10 minutes to form a charge generation layer having a layer thickness of 0.15 μm.

ポリカーボネート樹脂（商品名：ユーピロンＺ４００、三菱エンジニアリングプラスチックス（株）社製） １００部
次に、上記の材料をモノクロロベンゼン６００部／メチラール２００部の混合溶剤に溶解させて、第一の電荷輸送層用塗布液を調製した。
この第一の電荷輸送層用塗布液を電荷発生層上に浸漬塗布し、６０分間１００℃のオーブンで乾燥（加熱乾燥）させることにより、層厚が１５μｍの第一の電荷輸送層を形成した。 70 parts of a triarylamine compound (charge transport material) represented by the following structural formula (2)

Polycarbonate resin (trade name: Iupilon Z400, manufactured by Mitsubishi Engineering Plastics Co., Ltd.) 100 parts Next, the above material is dissolved in a mixed solvent of 600 parts of monochlorobenzene / 200 parts of methylal to obtain a first charge transport layer. A coating solution was prepared.
The first charge transport layer coating solution was dip-coated on the charge generation layer and dried (heat-dried) in an oven at 100 ° C. for 60 minutes to form a first charge transport layer having a layer thickness of 15 μm. .

次に、上記の材料を１，１，２，２，３，３，４−ヘプタフルオロシクロペンタン５０部／１−プロパノール５０部の混合溶剤に添加して第二の電荷輸送層用塗料の液状成分を調製した。 100 parts of a hole transporting compound represented by the following structural formula (3)

Next, the above-mentioned material is added to a mixed solvent of 1,1,2,2,3,3,4-heptafluorocyclopentane 50 parts / 1-propanol 50 parts to form a second charge transport layer coating liquid. Ingredients were prepared.

次に、第二の電荷輸送層用塗料の液状成分に不溶な物質である上記の材料をアセトン９０部に溶解させて溶液を調製した。
この溶液を、多孔性構造を有する架橋スチレン−アクリル中空粒子（粒子外径１．１μｍ、内径０．９μｍ）１５部に少量ずつ添加してアセトンを自然乾燥させ、構造式（４）を含有する多孔性粒子粉末を得た。 10 parts of a compound represented by the following structural formula (4)

Next, the above-mentioned material, which is a substance insoluble in the liquid component of the second charge transport layer coating material, was dissolved in 90 parts of acetone to prepare a solution.
This solution is added little by little to 15 parts of a crosslinked styrene-acrylic hollow particle having a porous structure (particle outer diameter 1.1 μm, inner diameter 0.9 μm), and acetone is naturally dried to contain structural formula (4). Porous particle powder was obtained.

  Next, this porous particle powder was added to the liquid component of the second charge transport layer coating material described above, and subjected to an ultrasonic dispersion treatment for 20 minutes to prepare a second charge transport layer coating material. At this time, the dispersibility of the porous particles in the paint was good.

Using this paint, the second charge transport layer was applied onto the first charge transport layer to form a coating film, and then pre-dried in an oven at a temperature of 50 ° C. for 10 minutes in the atmosphere. Thereafter, irradiation with an electron beam was performed for 1.6 seconds in a nitrogen atmosphere in which the oxygen concentration was kept at 15 ppm or less, while rotating the cylinder at 300 rpm under the conditions of an acceleration voltage of 70 kV and a beam current of 6.0 mA. Subsequently, the temperature was raised from 25 ° C. to 110 ° C. over 30 seconds in nitrogen to carry out a curing reaction. In addition, when the absorbed dose of the electron beam at this time was measured, it was 15 × 10 ³ Gy. The oxygen concentration in the heat curing reaction atmosphere was 15 ppm or less. Thereafter, this is taken out into the atmosphere, naturally cooled to a temperature of 25 ° C., and then subjected to a post-heating treatment in an oven at a temperature of 100 ° C. for 30 minutes to form a second charge transport layer having a thickness of 5 μm. An electrophotographic photoreceptor having the charge transport layer as the outermost layer was obtained.

<Image evaluation>
Using the electrophotographic photoreceptor thus obtained, image flow was evaluated in an environment of temperature 32.5 ° C./humidity 80% RH. The electrophotographic photoreceptor was used for evaluation after being left in the environment for 15 hours or more.
For the evaluation of image flow, a modified electrophotographic copying machine iR2870 manufactured by Canon Inc. was used so that the image exposure amount could be adjusted. The charging method is a contact charging method using a charging roller to which an AC / DC bias is superimposed and applied, and the AC bias is 2.5 kHz and 1.7 kVpp. The dark part potential (VD) was adjusted by adjusting the DC bias, and the bright part potential (VL) was adjusted by adjusting the image exposure amount. The surface potential was measured using a commercially available surface potential meter (trade name: surface potential meter MODEL344, manufactured by Trek Japan Co., Ltd.).
A photoconductor is mounted on this remodeling machine, the charging conditions and image exposure are adjusted so that VD is -700V and VL is -200V, and 1000 sheets are printed continuously at a printing rate of 1% and A4 paper size. It was. Subsequently, the entire surface character pattern was printed, and the image quality of the printed characters was visually evaluated as follows. The results are shown in Table 1.
A = Good state with no image defect B = Slight character blur but no problem in practical use C = Character blur is seen in part of the image D = Character blur occurs on the entire image However, it will be a problem in actual use

<Evaluation of degree of cure>
The surface layer at a position 180 mm from the upper end of the photoreceptor was peeled off with a razor, and the infrared spectroscopic total reflection measurement was performed on the surface layer fragment to calculate the uncured residual group IR peak ratio. As the infrared spectrometer, Spectrum One FT-IR Spectrometer manufactured by Perkin Elmer Instruments was used. The uncured residual group IR peak ratio has a wave number range of 1400.32 cm ⁻¹ or more and 1413.82 cm ⁻¹ or less, the peak area of the terminal olefin (CH ₂ ═) of the acryloyloxy group, 1699.29 cm ⁻¹ or more and 1770.65 cm ^−. A wave number range of ¹ or less was calculated as the peak area of the carbonyl (C═O) of the acryloyloxy group. The results are shown in Table 1.

[Example 2]
The surface of the electrophotographic photosensitive member obtained in Example 1 was roughened with the following polishing sheet and polishing conditions to obtain an electrophotographic photosensitive member having a roughened surface.
Polishing sheet: Width = 360 mm, base material = polyethylene, thickness = 75 μm,
Abrasive grain = SiC
Polishing conditions: polishing sheet tension = 1 mN, polishing time = 12 seconds,
Sheet feed time = 400 mm / min, work rotation speed = 240 rpm,
Work push-in amount = 3.0mm
The workpiece pushing amount is an amount of pushing the workpiece against a sponge roller having an Asker C hardness of 20 ° which is placed at a position facing the sheet with the sheet sandwiched when viewed from the workpiece side.
When the surface roughness of the obtained electrophotographic photosensitive member was measured with the following measuring machine and conditions, Rz (10-point average surface roughness) was 0.38 μm.
Measuring machine: Contact type surface roughness measuring machine (trade name: Surfcorder SE3500, manufactured by Kosaka Laboratory Ltd.)
Measurement conditions: Detector = R2 μm, 0.7 mN diamond needle,
Filter = 2CR, Cutoff value = 0.8 mm, Measurement length = 2.5 mm,
Feed rate = 0.1 mm, JIS standard 1982, 10-point average surface roughness Rz data
Process.
The obtained electrophotographic photoreceptor was evaluated in the same manner as in Example 1. The results are shown in Table 1.

[Comparative Example 1]
In Example 1, an electrophotographic photosensitive member was prepared in the same manner as in Example 1 except that only the liquid component was used as the second charge transport layer coating material and the compound of the structural formula (4) and the hollow particles were not used. In the same manner as in Example 1, the evaluation was made. The results are shown in Table 1.

[Comparative Example 2]
The electrophotography was carried out in the same manner as in Example 1, except that the compound of the structural formula (4) was not used and a coating material in which only hollow particles were dispersed in the liquid component was used as the second charge transport layer coating material. A photoconductor was prepared and evaluated in the same manner as in Example 1. The results are shown in Table 1.

[Comparative Example 3]
In Example 1, 30 parts of the compound of the structural formula (4) was added to 600 parts of the liquid component of the second charge transport layer coating material, stirred, and allowed to stand. As a result, precipitation of the compound occurred. The liquid and sediment were dispersed for 1 hour in a sand mill using glass beads having a diameter of 1 mm, and the glass beads were separated using a mesh. Furthermore, it filtered with the polyflon filter (brand name: PF-020, Advantech Toyo Co., Ltd. product), and prepared the coating material for 2nd electric charge transport layers. An electrophotographic photoreceptor was prepared in the same manner as in Example 1 except that this paint was used, and evaluated in the same manner as in Example 1. The results are shown in Table 1.

[Comparative Example 4]
In Comparative Example 3, 10 parts of the compound of the structural formula (4) was added to 200 parts of the liquid component of the second charge transport layer coating material, stirred, allowed to stand, and then removed from the precipitated compound. Filtration was performed with a filter (trade name: PF-020, manufactured by Advantech Toyo Co., Ltd.) to prepare a second paint for a charge transport layer. An electrophotographic photoreceptor was prepared in the same manner as in Example 1 except that this paint was used, and evaluated in the same manner as in Example 1. The results are shown in Table 1.
From Table 1, it can be seen that the electrophotographic photosensitive member produced by the method for producing an electrophotographic photosensitive member of the present invention has an effect of suppressing image flow, and the inhibition of curing of the outermost surface layer is also suppressed. It can also be seen that the effect of suppressing image blur is increased by subjecting the outermost surface layer to a roughening treatment.

DESCRIPTION OF SYMBOLS 1 ... Conductive support body 2 ... Conductive layer 3 ... Intermediate layer 4 ... Charge generation layer 5 ... Charge transport layer 6 ... Second charge transport layer (outermost surface layer)
7 ... Porous particles containing active substances

Claims (4)

A method for producing an electrophotographic photosensitive member having an outermost surface layer containing a curable resin, the production method comprising the following steps:
(A) a step of preparing a solution by dissolving a substance insoluble in the liquid medium of the coating material for the outermost surface layer containing the curable material in a solvent;
(B) a step of immersing porous particles in the solution obtained in step (A) to obtain porous particles containing the substance;
(C) step said porous particles obtained in (B) is dispersed in the liquid medium preparing a coating the outermost surface layer,
(D) Step step by coating the outermost surface layer coating material obtained in (C) to form a coating film, and step (E) to cure the coating film formed in (D) the outermost layer process for producing an electrophotographic photoreceptor characterized by having a step of forming. Wherein the porous particles of styrene - The method for producing an electrophotographic photosensitive member according to Oh Ru請 Motomeko 1 particles formed of acrylic copolymer resins. The substance insoluble in the liquid medium of the outermost surface layer coating material is at least one selected from the group consisting of alkylamine compounds, diamine compounds, cyclic amine compounds, hindered amine compounds, and hindered phenol compounds. A process for producing an electrophotographic photoreceptor according to 1. The method for producing an electrophotographic photosensitive member according to claim 1, wherein the curable material is a monomer and / or an oligomer having a charge transporting group.

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