Patent Application
20070154826
The present invention relates to an electrophotographic photoreceptor used for electrophotographic apparatuses such as copying machines, LED, LD printers, etc. and particularly to an electrophotographic photoreceptor which has an undercoat layer and uses an organic photoconductive material, and an electrophotographic apparatus provided with the photoreceptor.
In general, an electrophotographic process using a photoreceptor is performed in the following manner. That is, the photoreceptor is charged in the dark by a charging roller in the case of, for example, a contact charging method, and then exposed using LED or LD as an imagewise exposing means to selectively dissipate the charge in only the exposed areas to form an electrostatic latent image, which is rendered visible with a developer to form an image.
Fundamental properties required for the electrophotographic photoreceptors are such functions that they can be charged to a proper potential in the dark and the surface charge can be dissipated by irradiation with light.
Electrophotographic photoreceptors which are now put to practical use basically comprise a conductive support and a photosensitive layer formed thereon. However, these photoreceptors suffer from the problems that when an aluminum tube as a conductive support is subjected to cutting process by a diamond cutting tool or the like, cutting oil or powders remain on the support and appear as defects at the time of formation of images after the photosensitive layer is coated on the support or when a high voltage is applied to the surface of the photoreceptor, current flows into the photoreceptor through the defects such as cutting burrs and deposited dirt or foreign matters to result in partial short-circuits. Furthermore, they appear as image defects such as dusts and fogs. Moreover, the charge generation layer formed on the conductive substrate has a thickness of about 1 μm, and is influenced by these defects to adversely affect the functions as a photoreceptor.
For inhibition of adverse effects caused by the defects on the surface of the conductive substrate, there is usually employed a method of covering the defects on the conductive substrate by providing an Alumite coat (anodized aluminum coat) on the substrate by anodizing treatment or by providing an undercoat layer using resin materials.
However, the Alumite coat has the disadvantages such as inclusion of dirt in the fine pores formed on the surface of the Alumite coat during the formation of the coat and contamination of the surface of the Alumite coat caused at the sealing step of pores or cleaning step. Thus, even if the defects on the surface of the conductive substrate are covered, contamination of the Alumite coat per se adversely affects the photoreceptor.
It is known that resin materials such as polyethylene, polypropylene, polystyrene, acrylic resin, vinyl chloride resin, vinyl acetate resin, polyurethane resin, epoxy resin, silicone resin and polyamide resin are used for the undercoat layer. Of these resins, polyamide resins are particularly preferred.
However, in the case of an electrophotographic photoreceptor in which polyamide resin or the like is used for the undercoat layer, since the volume resistivity of the photoreceptor is about 1012-1015 Ω·cm, residual potential is accumulated in the photoreceptor unless the undercoat layer is made thin to a thickness of 1 μm or less, and as a result, dusts or fogs occur in the resulting images. On the other hand, if the undercoat layer is made thin, not only the defects on the conductive support cannot be covered, but also injection of holes from the substrate is accelerated during repeated use to cause considerable reduction of charging potential and decrease of photosensitivity, resulting in formation of dusts and fogs in the image to damage the image quality.
An undercoat layer is proposed which comprises a polyimide resin soluble in an organic solvent and has a thickness of 0.5 μm (e.g. Patent Document 1).
Patent Document 1: JP-A-8-30007
However, it has been found that in the case of combining the conventional charge transport agent with the undercoat layer comprising a polyimide resin and having a thin thickness of less than 1.0 μm as disclosed in Patent Document 1, the residual potential after repeated use of the photoreceptor increases, resulting in dusts and fogs in the image.
Furthermore, in the case of the electrophotographic apparatus provided with a contact charging member which applies a charging voltage by directly contacting the undercoat layer with photoreceptor, a high voltage is directly applied to the electrophotographic photoreceptor, and hence dusts and fogs are often generated.
The object of the present invention is to provide an electrophotographic photoreceptor which is excellent in repetition stability and environmental characteristics by covering the defects on the conductive substrate without damaging the excellent electrophotographic characteristics.
As a result of intensive research conducted by the inventors in an attempt to solve the above problems, it has been found that an electrophotographic photoreceptor comprising a conductive support and a photosensitive layer formed on the conductive support, with an undercoat layer provided therebetween, is free from the above problems in the conventional technologies and maintains excellent electrostatic characteristics over a long period of time in case the undercoat layer contains a specific polyimide resin and a specific charge generation agent. Thus, the present invention has been accomplished.
That is, the present invention relates to an electrophotographic photoreceptor comprising a conductive support and a photosensitive layer formed thereon, with an undercoat layer provided between the support and the photosensitive layer, characterized in that the undercoat layer contains a polyimide resin and the photosensitive layer contains, as a charge generation agent, oxytitanium phthalocyanine showing a main diffraction peak intensity at a Bragg angle (2θ±0.2°) of 27.30° in X-ray diffraction spectrum when measured using CuKα as a radiation source.
According to the invention described in claim 1 having the above construction, the defects of the conductive support such as pin holes can be covered and furthermore increase of residual potential after repeated use can be inhibited and generation of dusts and fogs on the image can be prevented.
The invention described in claim 2 relates to an electrophotographic photoreceptor, wherein the undercoat layer contains a polyimide resin represented by the following formula [I].
Formula [I]
(in the formula, X is a divalent polycyclic aromatic group in which the aromatic rings may be linked by a hetero-atom and n is an integer which shows a polymerization degree).
According to the invention described in claim 2 having the above construction, increase of residual potential after repeated use can be inhibited.
The invention described in claim 3 relates to an electrophotographic photoreceptor of claim 1, wherein the undercoat layer has a thickness of 3.0-50 μm.
According to the invention described in claim 3 having the above construction, even relatively large defects on the conductive support can be covered and the resulting image is free from defects.
The invention described in claim 4 relates to an electrophotographic photoreceptor of claim 1, wherein the undercoat layer contains titanium oxide, whereby the permittivity of the undercoat layer can be enhanced and dispersibility is also improved. Moreover, it is preferred that the weight ratio of the polyimide resin and titanium oxide is in the range of 3:1-1:4.
The invention described in claim 5 relates to an electrophotographic photoreceptor of claim 1, wherein the undercoat layer has a two-layer structure comprising a layer containing a polyimide resin represented by the formula [I] and a layer comprising a thermosetting resin or a thermoplastic resin provided on the layer containing polyimide resin, whereby even if the undercoat layer is thick, accumulation of the residual potential can be inhibited and chargeability can be stabilized, resulting in improvement in image quality.
The invention described in claim 6 relates to an electrophotographic photoreceptor of claim 1, wherein a tube which is not subjected to cutting process is used as the conductive support, whereby the defects on the surface of the conductive support can be surely covered.
The invention described in claim 7 relates to an electrophotographic apparatus using the electrophotographic photoreceptor of claims 1-6, wherein a contact charging means is provided as a charging means, whereby the object of the present invention can be attained.
The invention described in claim 8 relates to an electrophotographic apparatus using the electrophotographic photoreceptor of claims 1-6, wherein an exposing means uses a semiconductor laser, whereby the problem of interference fringes in the image can be solved.
In the electrophotographic photoreceptor of the present invention, electrostatic characteristics such as surface potential and potential after exposure are not greatly deteriorated even after repeated use, no image defects occur and repetition stability is high.
Therefore, according to the present invention, there can be provided an electrophotographic photoreceptor which has excellent electrophotographic characteristics, cleanability and oil resistance and, besides, can be simplified in its maintenance.
The preferred embodiments of the electrophotographic photoreceptor according to the present invention will be explained in detail below.
The present invention is applied to, for example, a double-layered type electrophotographic photoreceptor comprising a conductive support, a charge generation layer containing at least a charge generation agent and formed on the support, and a charge transport layer containing at least a charge transport agent and formed on the charge generation layer. In this case, the photosensitive layer is formed of the charge generation layer and the charge transport layer.
Furthermore, the present invention can also be applied to a monolayer type electrophotographic photoreceptor in which the charge generation agent and the charge transport agent are contained in the same layer or an inversely laminated type electrophotographic photoreceptor in which the charge transport layer is first formed and thereafter the charge generation layer is laminated thereon.
As the conductive support usable in the present invention, various materials having electrical conductivity can be used with no limitation in the kind and shape thereof, and examples of the materials are worked pieces of metals or alloys thereof such as aluminum, brass, stainless steel, nickel, chromium, titanium, gold, silver, copper, tin, platinum, molybdenum and indium, plastic sheets or films to which electrical conductivity is imparted by vacuum deposition or plating of the above metals or conductive materials such carbon, conductive glasses made by coating with tin oxide, indium oxide, aluminum iodide, and the like. As for the shape of the conductive supports, there may be used those which have a shape of drum, rod, plate, sheet or belt.
Among them, suitable are aluminum alloys of JIS3000 series, JIS5000 series, JIS6000 series, etc., which are shaped by general methods such as EI method, ED method, DI method, and II method, and preferred are uncut tubes which are not subjected to surface cutting process using a diamond cutting tool or surface treatments such as abrasion and anodizing treatments.
The charge generation agents usable in the present invention are preferably disazo pigments and oxytitanium phthalocyanine because they have good affinity in sensitivity. Particularly, oxytitanium phthalocyanine is reported to have many crystal forms, and, among them, especially preferred for the electrophotographic photoreceptor of the present invention is oxytitanium phthalocyanine showing a main diffraction peak intensity at a Bragg angle (2θ±0.2°) of 27.3° in X-ray diffraction spectrum when measured using CuKα as a radiation source. The thickness is 0.01-5.0 μm, preferably 0.1-1.0 μm.
The charge generation agent may be used each alone or in admixture of two or more for obtaining proper light sensitivity wavelength or sensitization action.
The undercoat layer in the present invention may contain an intermediate before polyimidation, and the mixing ratio of the polyimide precursor and the polyimide resin is such that the polyimide resin is contained in an amount of suitably 20-70%, preferably 30-50% based on the total weight of the polyimide resin and the polyimide precursor. If the content of the polyimide resin is less than 20%, the undercoat layer dissolves in the organic solvent, and if it is more than 70%, the intermediate is in nearly imidated state, resulting in accumulation of residual potential after repeated use and deterioration in image quality.
The molecular weight of the polyimide resin is preferably 1,000-100,000, especially preferably 10,000-30,000. Examples of X in the formula [I] are as follows.
In the electrophotographic photoreceptor of the present invention comprising a conductive support and a photosensitive layer formed on the support, with an undercoat layer provided therebetween, the undercoat layer contains a polyimide resin represented by the formula [I] whereby film formability is improved, defects such as pin holes on the conductive support can be covered even when the layer is thin, and the photosensitive layer is superior in barrier function and adhesion function. The thickness is 3.0-50 μm, preferably 5-30 μm.
The drying temperature in formation of the undercoat layer is suitably 110-170° C., preferably 130-150° C. If it is lower than 110° C., the undercoat layer dissolves in the solvent and hence cannot be coated on the photoreceptor. If the undercoat layer is dried at 110° C. or higher, it does not dissolve in the organic solvent. If the drying temperature is higher than 170° C., the residual potential after repeated use increases to cause change in image density.
Further, when the undercoat layer has a two-layer structure comprising a layer containing a polyimide resin represented by the formula [I] and a layer comprising a thermosetting resin or a thermoplastic resin provided thereon, even if the thickness of the undercoat layer increases, the accumulation of residual potential can be inhibited and besides quality of image is improved.
In the electrophotographic photoreceptor of the present invention, the undercoat layer may contain titanium oxide. The surface of titanium oxide particles used in the present invention may be subjected to various treatments so long as they do not reduce volume resistivity. For example, the particle surface can be coated with an oxide film using aluminum, silicon, nickel or the like as a treating agent. In addition, if necessary, water repellency can be imparted to the particles using a coupling agent or the like. The average particle diameter of the titanium oxide is preferably 1 μm or less, more preferably 0.01-0.5 μm. The content of the titanium oxide is preferably 0.5-4 when the amount of the polyimide is assumed to be 1.
Furthermore, the undercoat layer may have a two-layer structure of a layer comprising a polyimide resin and a layer comprising a thermosetting resin or a thermoplastic resin provided thereon. As the thermosetting resin, mention may be made of epoxv resin, polyurethane resin, phenolic resin, melamine-alkyd resin, unsaturated polyester resin, etc. As the thermoplastic resin, mention may be made of syrene-based elastomers, olefin-based elastomers, urethane-based elastomers, polyvinyl chloride-based elastomers, etc. The thickness of the resin layer provided on the polyimide resin layer is 0.1-10.0 μm, preferably 0.8-5.0 μm.
Both or one of the two layers may contain a white pigment for the purpose of inhibiting interference of light during exposure with semiconductor laser. Examples of the white pigment are titanium oxide, zinc oxide, silica, etc.
Binder resins used for the formation of the photosensitive layer include, for example, photosetting resins such as polycarbonate resin, styrene resin, acrylic resin, styrene-acryl resin, ethylene-vinyl acetate resin, polypropylene resin, vinyl chloride resin, chlorinated polyether, vinyl chloride-vinyl acetate resin, polyester resin, furan resin, nitrile resin, alkyd resin, polyacetal resin, polymethylpentene resin, polyamide resin, polyurethane resin, epoxy resin, polyarylate resin, diarylate resin, polysulfone resin, polyether sulfone resin, polyallyl sulfone resin, silicone resin, ketone resin, polyvinyl butyral resin, polyether resin, phenolic resin, EVA (ethylene•vinylacetate copolymer) resin, ACS (acrylonitrile•chlorinated polyethylene•styrene) resin, ABS (acrylonitrile•butadiene•styrene) resin, and epoxy arylate. These may be used each alone or in admixture of two or more. Moreover, when resins differing in molecular weight are used in admixture, hardness and abrasion resistance can be improved, which is more preferred.
As the charge transport materials used in the present invention, preferred are compounds shown by the formulas [II] and/or [III].
Formula [II]
(in the above formula, R1-R5 independently represent a hydrogen atom, a halogen atom, an alkyl group having 1-6 carbon atoms which may have a substituent or a substituted or unsubstituted aryl group having 6-12 carbon atoms, and h represents an integer of 0 or 1).
Formula [III]
(in the above formula, R6-R9 may be the same or different and independently represent a hydrogen atom, a halogen atom, an alkyl group or alkoxy group having 1-6 carbon atoms or an aryl group which may have a substituent, R10 represents a hydrogen atom, a halogen atom, an alkyl group or alkoxy group having 1-6 carbon atoms, an aryl group which may have a substituent, an alkenyl group or alkadienyl group which may have a substituent or a group represented by the following formula [IV], and n represents an integer of 0 or 1).
Formula [IV]
(in the above formula, R11 and R12 may be the same or different and independently represent a hydrogen atom, a halogen atom, an alkyl group or alkoxy group having 1-6 carbon atoms or an aryl group which may have a substituent, and n represents an integer of 0 or 1).
The above charge transport materials are high in affinity with oxytitanium phthalocyanine, and the electrophotographic photoreceptor of the present invention shows excellent electrical characteristics of high sensitivity and low residual potential.
Among the compounds represented by the formula [II], particularly the compounds represented by the following formulas [V] and [VI] are high in affinity with oxytitanium phthalocyanine and are preferred.
Furthermore, among the compounds represented by the formula [III], particularly the compounds represented by the following formulas [VII], [VIII], [IX] and [X] are high in affinity with oxytitanium phthalocyanine and are preferred.
When the compound selected from those of the formula [II] and the compound selected from those of the formula [III] are used simultaneously as the charge transport materials, good characteristics are also obtained.
Other charge transport materials than those mentioned above can also be used. The other charge transport materials include polyvinyl carbazole, halogenated polyvinyl carbazole, etc.
Furthermore, other charge transport materials can be added to the photosensitive layer of the electrophotographic photoreceptor of the present invention. In this case, the sensitivity of the photosensitive layer can be enhanced or the residual potential can be reduced, and hence the characteristics of the electrophotographic photoreceptor of the present invention can be improved.
As the other charge transport materials which can be added for improving the characteristics, there may be used conductive high molecular compounds such as polyvinyl carbazole, halogenated polyvinyl carbazole, polyvinylpyrene, polyvinylindoloquinoxaline, polyvinylbenzothiophene, polyvinylanthracene, polyvinylacridine, polyvinylpyrazoline, polyacetylene, polythiophene, polypyrrole, polyphenylene, polyphenylenevinylene, polyisothianaphthene, polyaniline, polydiacetylene, polyheptadiene, polypyridinediyl, polyquinoline, polyphenylene sulfide, polyferrocenylene, polyperinaphthylene, and polyphthalocyanine.
Moreover, as the charge transport materials, there may also be added low molecular compounds, e.g., polycyclic aromatic compounds such as trinitrofluorenone, tetracyanoethylene, tetracyanoquinodimethane, quinone, diphenoquinone, naphthoquinone, anthraquinone and derivatives thereof, anthracene, pyrene and phenanthrene, nitrogen-containing heterocyclic compounds such as indole, carbazole and imidazole, fluorenone, fluorene, oxadiazole, oxazole, pyrazoline, triphenylmethane, triphenylamine, enamine, stilbene, other butadiene than those mentioned above, other hydrazone compounds than those mentioned above, and the like.
As charge transport materials used for the similar purpose, there may be added high-molecular solid electrolytes obtained by doping high-molecular compounds such as polyethylene oxide, polypropylene oxide, polyacrylonitrile and polymethacrylic acid with a metal ion such as Li (lithium) ion.
As additional charge transport materials used for the similar purpose, there may be used organic charge-transfer complexes comprising an electron donor substance and an electron acceptor substance such as tetrathiafurvalene-tetracyanoquinodimethane.
The desired photoreceptor characteristics can be obtained by using one charge transport agent or two or more charge transport agents as a mixture. The thickness of the charge transport layer is 5.0-50 μm, preferably 10-30 μm.
In the electrophotographic photoreceptor of the present invention, the total thickness of the photosensitive layer is 10-50 μm, preferably 15-25 μm. For example, in case the undercoat layer is provided in a large thickness of about 25 μm, the charge transport layer may be provided in a thin thickness of about 15 μm. On the other hand, in case the undercoat layer is provided in a thin thickness of about 1 μm, the charge transport layer may be provided in a large thickness of about 25 μm.
This is because the photoreceptor is required to have pressure resistance in electrophotographic process using a contact charging means as a charging means. Generally, in the case of a photoreceptor of low pressure resistance, defects occur inside the photoreceptor and on the surface of the photoreceptor due to leakage of current, and the defects appear as defects of image. That is, since the pressure resistance of the photoreceptor is determined by the total thickness of the photoreceptor, when the undercoat layer is thick, the pressure resistance is improved and hence the charge transport layer can be made thin.
It is preferred for the electrophotographic photoreceptor of the present invention that the photosensitive layer contains an antioxidant or an ultraviolet absorber for inhibiting change of characteristics and occurrence of cracks caused by oxidative deterioration of photoconductive materials or binder resins and for improving mechanical strength.
The antioxidants used in the present invention are preferably monophenols such as 2,6-di-tert-butylphenol, 2,6-di-tert-4-methoxyphenol, 2-tert-butyl-4-methoxyphenol, 2,4-dimethyl-6-tert-butylphenol, 2,6-di-tert-butyl-4-methylphenol, butylated hydroxyanisole, stearyl-β-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate, α-tocopherol, β-tocopherol and n-octadecyl-3-(3′-5′-di-tert-butyl-4′-hydroxyphenyl) propionate, and polyphenols such as 2,2′-methylenebis(6-tert-butyl-4-methylphenol), 4,4′-butylidene-bis-(3-methyl-6-tert-butylphenol), 4,4′-thiobis(6-tert-butyl-3-methylphenol), 1,1,3-tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane, 1,3,5-trimethyl-2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)benzene and tetrakis[methylene-3(3,5-di-tert-butyl-4-hydroxyphenyl) propionate]methane. These can be contained in the photosensitive layer each alone or in combination of two or more.
The ultraviolet absorbers are preferably benzotriazole-based absorbers such as 2-(5-methyl-2-hydroxyphenyl)benzotriazole, 2-[2-hydroxy-3,5-bis( α,αdimethylbenzyl)phenyl]-2H-benzotriazole, 2-(3,5-di-tert-butyl-2-hydroxyphenyl)benzotriazole, 2-(3-tert-butyl-5-methyl-2-hydroxyphenyl)-5-chlorobenzotriazole, 2-(3,5-di-tert-butyl-2-hydroxyphenyl)-5-chlorobenzotriazole, 2-(3,5-di-tert-amyl-2-hydroxyphenyl)benzotriazole and 2-(2′-hydroxy-5′-tert-octylphenyl)benzotriazole, and salicylic acid-based absorbers such as phenyl salicylate, p-tert-butylphenyl salicylate and p-octylphenyl salicylate. These can be contained in the photosensitive layer each alone or in combination of two or more.
The antioxidant and the ultraviolet absorber can be simultaneously added. These can be added to any layer in the photosensitive layer, but it is preferred to add them to the outermost surface layer, particularly, the charge transport layer.
The amount of the antioxidant added is preferably 3-20% by weight based on the binder resin, and that of the ultraviolet absorber is preferably 3-30% by weight based on the binder resin. When both the antioxidant and the ultraviolet absorber are added together, the total amount of them is preferably 5-40% by weight based on the binder resin.
In addition to the antioxidant and the ultraviolet absorber, there may be added light stabilizers such as hindered amines and hindered phenols, aging inhibitors such as diphenylamine compounds, surface active agents, etc. to the photosensitive layer.
The general method for forming the photosensitive layer comprises dispersing or dissolving a given photosensitive material and a given binder resin in a solvent to prepare a coating solution and coating the solution on a given substrate.
The coating solution can be coated, depending on the shape of the substrate or state of the coating solution, by dip coating, curtain flow coating, bar coating, roll coating, ring coating, spin coating, spray coating, etc.
The charge generation layer can also be formed by vacuum deposition method.
The solvents used for coating solution include, for example, alcohols such as methanol, ethanol, n-propanol, i-propanol, butanol, methyl cellosolve and ethyl cellosolve, saturated aliphatic hydrocarbons such as pentane, hexane, heptane, octane, cyclohexane and cycloheptane, aromatic hydrocarbons such as toluene and xylene, chlorine-containing hydrocarbons such as dichloromethane, dichloroethane, chloroform and chlorobenzene, ethers such as dimethyl ether, diethyl ether and tetrahydrofuran (THF), ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone and cyclohexanone, esters such as ethyl formate, propyl formate, methyl acetate, ethyl acetate, propyl acetate, butyl acetate and methyl propionate, and amides such as N,N-dimethylformamide, dimethyl sulfoxide and N-methyl-2-pyrrolidone. These may be used each alone or in admixture of two or more.
Furthermore, an intermediate layer comprising a resin in which a metal compound, metal oxide, carbon, silica, resin powder or the like is dispersed can be provided on the undercoat layer. Moreover, it may contain various pigments, electron accepting substances, electron donating substances or the like for improvement of characteristics.
In addition, there may be formed a surface protective layer on the surface of the photosensitive layer by forming an organic thin film of polyvinyl formal resin, polycarbonate resin, fluorocarbon resin, polyurethane resin, silicone resin or the like or a thin film comprising a siloxane structure formed of a hydrolyzate of silane coupling agent, and, in this case, endurance of the photoreceptor is improved, which is preferred. The surface protective layer may be provided for improving functions other than the endurance.
Next, the electrophotographic process and electrophotographic apparatus of the present invention will be explained. For the electrophotographic process of the present invention, there may be used known means such as charging means, exposing means, developing means, transferring means, fixing means and cleaning means. For the charging means, a non-contact charging system such as corona charging system, and a contact charging system such as charging roller or charging brush can be used. As a light source for imagewise exposing means, there can be used halogen lamp, fluorescent lamp, laser beams, etc. The wavelength of semiconductor laser is 780 nm or less, preferably 780-500 nm, and, in this case, there may be employed such a method as of narrowing down the diameter of laser beam. The developing method includes any of dry developing method, wet developing method, two component developing method, one component developing method, and magnetic/non-magnetic developing method. The transferring means may be either roller or belt.
Examples and comparative examples of the electrophotographic photoreceptor according to the present invention will be explained in detail below.
A mixture comprising titanium oxide particles coated with alumina and a polyimide resin represented by the formula [I] in which X is [X−1] at a weight ratio of 1:1 was coated on a cylindrical drum of 30 mm in diameter comprising aluminum and subjected to no cutting process, followed by drying at 140° C. for 30 minutes to form a first undercoat layer of 18.0 μm in thickness. Then, on the first undercoat layer was coated a coating solution prepared by dissolving a melamine-alkyd resin as a thermosetting resin and titanium oxide at a ratio of 1:3 in methyl ethyl ketone to laminate a second undercoat layer having a thickness of 0.7 μm on the first undercoat layer.
Then, thereon was coated a dispersion of oxytitanium phthalocyanine having a main peak at an X-ray diffraction intensity (2θ±0.2) 27.3° (
Then, a coating solution was prepared by dissolving in chloroform a polycarbonate copolymer as a binder resin, a butadiene compound of the formula [VI] as a charge transport agent and 2,6-di-tert-butyl-4-methylphenol as an antioxidant at a weight ratio of polycarbonate copolymer/butadiene compound/2,6-di-tert-butyl-4-methylphenol=1.0/0.8/0.18.
The resulting coating solution was coated by dip coating, followed by drying at 100° C. for 1 hour to form a charge transport layer of 20 μm in thickness, thereby obtaining an electrophotographic photoreceptor.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the weight ratio of polyimide resin and titanium oxide in the first undercoat layer was changed to 2:1.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the weight ratio of polyimide resin and titanium oxide in the first undercoat layer was changed to 1:4.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the thickness of the first undercoat layer was changed to 3.0 μm.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the thickness of the first undercoat layer was changed to 5.0 μm.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the thickness of the first undercoat layer was changed to 13.0 μm.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the thickness of the first undercoat layer was changed to 30.0 μm.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the thickness of the first undercoat layer was changed to 50.0 μm.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the second undercoat layer was omitted.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the charge transport agent of the formula [VI] used was changed to that of the formula [VII].
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the thickness of the first undercoat layer was changed to 2.0 μm.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the charge transport agent of the formula [VI] used was changed to that of the formula [V].
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the charge generation agent used was changed to a charge generation agent having a maximum peak at an X-ray diffraction intensity 7.5°.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that an Alumite layer was formed by anodizing treatment in place of the undercoat layer formed in Example.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the first undercoat layer was omitted.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that the first undercoat layer and the second undercoat layer were omitted.
An electrophotographic photoreceptor was prepared in the same manner as in Example 1, except that a bisazo compound was used in place of the charge generation agent used in Example 1.
Evaluation Method
[Measurement of Electrostatic Characteristics, Repeated Cycling Test, Image Test]
The cylindrical electrophotographic photoreceptors prepared in Examples 1-12 and Comparative Examples 1-5 were charged using a direct charging type Microline 14 printer manufactured by Oki Data Co., Ltd. in an environment of normal temperature and humidity (24° C., 40% RH) so that the photoreceptors after charged had a surface potential of −800 V, and were subjected to initial setting so that the photoreceptors after exposed by LED had a surface potential of −50 V. Then, after printing of 20,000 copies of A4 size, the surface potential V0 (−V) and the residual potential VR (−V) were measured. The image test was conducted by evaluating the images after continuous printing of 20,000 copies. The results are shown in Table 1. In Table 1, the mark “◯” means that the resulting image was good in quality and “X” means that the resulting image was defective and practically unacceptable.
As is clear from Table 1, the electrophotographic photoreceptors of Examples 1-12 were satisfactory in chargeability and less in light-induced fatigue even after repeated printing of 20,000 copies, and, furthermore, there occurred no defects in the resulting images such as dusts and fogs.
In addition, good results were also obtained when titanium oxide was added to the polyimide resin or thermosetting resin or thermoplastic resin was laminated on the polyimide resin layer.
That is, the results were particularly superior in Examples 1-12.
On the other hand, in case the polyimide resin layer was not present in Comparative Examples 3 and 4, black points due to transfer memory and dusts and fogs occurred.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2004-022753 | Jan 2004 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP04/19067 | 12/21/2004 | WO | 7/25/2006 |
