Patent Grant
7642025
This application is based on and claims priority under 35 USC 119 from Japanese Patent Application No. 2006-254760 filed Sep. 20, 2006.
1. Technical Field
The present invention relates to an electrophotographic photoreceptor, a method of producing the same, a process cartridge provided with the electrophotographic photoreceptor, and an image-forming apparatus.
2. Related Art
Digitalization of copiers and printers using an electrophotographic system has been advancing in recent years, and among these, those using a laser as an optical recording system are prevailing. Usually, a latent image is written by spot-scanning laser light in the axial direction of a photoreceptor with a laser scanning writing apparatus. Owing to cost reduction and miniaturization of polygon scanners, laser beam printers using an electrophotographic system have come to be used for personal use, but further cost reduction and miniaturization are essential for competing with printers using an inkjet method with which laser beam printers compete in the field of small printers.
In the laser scanning apparatus, there is distribution of light quantity due to aberration. Compensation for this distribution of light quantity by the system results in higher costs and thus cannot be used particularly for small printers.
According to an aspect of the present invention, there is provided an electrophotographic photoreceptor having a cylindrical support, and a charge-generating layer and a charge-transporting layer on or above the cylindrical support, wherein: the thickness of the charge-generating layer increases from a central portion in the axial direction of the cylindrical support towards both of end portions thereof; and the difference in thickness between the two end portions of the charge-generating layer is 2.5% or less with regard to an average thickness of the charge-generating layer.
Exemplary embodiments of the present invention will be described in detail based on the following figures, wherein:
In the exemplary embodiment of the present invention, the electrophotographic photoreceptor (hereinafter, may be referred to as a photoreceptor) has a cylindrical support, and a charge-generating layer and a charge-transporting layer on or above the cylindrical support, wherein: the thickness of the charge-generating layer increases from a central portion in the axial direction of the cylindrical support towards both end portions thereof; and the difference in thickness between the two end portions of the charge-generating layer is 2.5% or less with regard to an average thickness of the charge-generating layer.
As shown in
One example of the constitution of a laser scanning writing device used as an exposure unit is shown in
In the laser scanning writing device described above, the semiconductor laser 60 is driven by a laser driving part 68 in response to an image information signal, whereby a laser beam processed by collimation by the collimating lens 62 is output by a light source device depending on the image information. The laser beam is polarized by the polygon mirror 64. When an image is formed by main scanning, the position of light beam is detected with a scanning starting position sensor 70, thereby synchronizing the main scanning.
The polarized laser beam is condensed by the fθ lens 66 to form an image on the photoreceptor 10 serving as a surface scanned with the laser beam.
The fθ lens 66 is compensated such that the scanning speed becomes constant on the photoreceptor 10. A latent image corresponding to the image information is thereby formed on the photoreceptor 10.
Since the light quantity distribution of the laser beam has a Gaussian distribution around the center, as the scanning angle of the polygon mirror relative to the light axis of incident light is increased, the light quantity is the highest at the central portion in the axial direction of the photoreceptor, and the light quantity is decreased in the directions toward both end sides, as shown in
In the electrophotographic photoreceptor in this exemplary embodiment, therefore, the difference in thickness of the charge-generating layer between the two end portions in the axial direction of the photoreceptor is 2.5% or less of an average thickness of the charge-generating layer.
The image density unevenness in this exemplary embodiment is expressed following.
For example, when an image of 100% density is printed on a whole surface of recording medium, the image density unevenness in this exemplary embodiment is expressed by a difference in density between the output image in a part corresponding to the central portion in the axial direction of the charge-generating layer and the image at the end portion (positioned 2 mm toward the central portion from the end of the formed charge-generating layer in the axial direction. In
The image density is measured for example with a reflectance spectrophotometric densitometer (X-Rite 938 manufactured by X-Rite).
Hereinafter, the charge-generating layer and the method of producing thereof are first described, and then the electrophotographic photoreceptor having the charge-generating layer is described and further the process cartridge provided with the electrophotographic photoreceptor, and the image-forming apparatus, are described.
<Charge-Generating Layer>
The charge-generating layer contains at least a charge-generating material and a resin.
The charge-generating materials used include those known in the art, for example azo pigments such as bisazo and trisazo; condensed ring aromatic pigments such as dibromoanthanthrone; organic pigments such as perylene pigment, pyrroropyrrole pigment and phthalocyanine pigment; and inorganic pigments such as triclinic selenium and zinc oxide. In particularly, metal or nonmetal phthalocyanine pigments, triclinic selenium, and dibromoanthanthrone are preferable.
Particularly preferable among these are hydroxy gallium phthalocyanine disclosed in JP-A Nos. 5-263007 and 5-279591, chlorogallium phthalocyanine in JP-A No. 5-98181, dichlorotin phthalocyanine in JP-A Nos. 5-140472 and 5-140473, and titanyl phthalocyanine in JP-A Nos. 4-189873 and 5-43813.
The resin may be selected from a wide variety of resins, and preferable resins include, but are not limited to, polyvinyl butyral resin, polyarylate resin (polycondensate product of bisphenol A and phthalic acid, etc.), polycarbonate resin, polyester resin, phenoxy resin, vinyl chloride-vinyl acetate copolymer, polyamide resin, acryl resin, polyacrylamide resin, polyvinyl pyridine resin, cellulose resin, urethane resin, epoxy resin, casein, polyvinyl alcohol resin and polyvinyl pyrrolidone resin.
These resins may be used alone or in combination of two or more thereof. A material having both the function of the resin and the function of the charge-generating material, such as poly-N-vinyl carbazole, polyvinyl anthracene, polyvinyl pyrene and polysilane, may also be used.
The compounding ratio (weight ratio) of the charge-generating material to the resin is preferably in a range of 10:1 to 1:10 (=charge-generating material:resin). As the method of dispersing them, usual methods such as a ball mill dispersion method, an atrighter dispersion method or a sand mill dispersion method may be used.
In dispersion, it is effective for the size of the particle to be reduced to a size of 0.5 μm or less, preferably 0.3 μm or less, more preferably 0.15 μm or less. As the solvent used in dispersion, an usual organic solvent such as methanol, ethanol, n-propanol, n-butanol, benzyl alcohol, methyl Cellosolve, ethyl Cellosolve, acetone, methyl ethyl ketone, cyclohexanone, methyl acetate, n-butyl acetate, dioxane, tetrahydrofuran, methylene chloride, chloroform, chlorobenzene and toluene may be used. These solvents may be used alone or in combination of two or more thereof.
In the charge-generating layer in this exemplary embodiment, the thickness is increased from the central portion in the directions towards both end portions in the axial direction of the cylindrical support. When the thickness of the charge-generating layer is increased from the central portion in the directions towards both end portions, there is unevenness in a minute region due to surface roughness and undulation, so the thickness of the layer may be transiently reduced in the directions toward both the end portions.
In this exemplary embodiment, the thickness of the charge-generating layer is measured by a photoabsorption method. The photoabsorption method utilizes the phenomenon in which the absorbed amount of light having a certain wavelength is varied depending on the thickness of a light-absorbing layer, and this method is used often for measurement of the thickness of a charge-generating layer in an electrophotographic photoreceptor.
In this exemplary embodiment, a sample having the charge-generating layer formed thereon is irradiated with light from a halogen lamp as an irradiating light source by guiding the light via an optical fiber to measurement places on the sample, and the intensity of the reflected light is measured at intervals of every 10 nm with a spectrophotometer to obtain light quantity data, to thereby calculate the ratio of the intensity of the reflected light at a wavelength of 750 nm to the maximum intensity of the reflected light in the visible light range (400 nm to 800 nm) as the spectroscopic absorption ratio (=“light intensity at a wavelength of 750 nm”/“maximum light intensity in the visible light range (400 nm to 800 nm)”). A spectroscopic absorption ratio obtained using films of known thickness is used to prepare a calibration curve, on the basis of which the thickness of a film that is the object of measurement is determined.
From the viewpoint of suppressing generation of image density unevenness, the difference in thickness between the two end portions of the charge-generating layer in the axial direction of the photoreceptor is 2.5% or less of an average layer thickness, more preferably 2.0% or less, and still more preferably 1.5% or less.
The average thickness is the arithmetic average of layer thickness determined at 15° intervals in the circumferential direction and at 5-mm intervals in the axial direction of the cylindrical support by the method described above.
As used herein, the end portion refers to a portion that is 2 mm toward the central portion from the end of the charge-generating layer in the axial direction. This definition of the end portion applies hereinafter. For example, as shown in
The closer the end portion is to the end of the cylindrical support in the axial direction, the greater the region (effective region) where an image can be formed on the photoreceptor becomes and smaller an area where an image is not formed becomes, so that an image of equivalent size can be forming using a smaller image-forming apparatus. A length of an effective region is defined as the length of an image of constant quality in the axial direction of the photoreceptor and satisfying a standard of quality in each image-forming apparatus, and the effective region is a region wherein differences in image density in a printed image formed at 100% image density, with respect to an image density at a part corresponding to the central portion in the axial direction of the charge-generating layer, are within 0.25D.
The length of the effective region of a general photoreceptor is shown in Table 1 below. On the other hand, the length of the effective region of a photoreceptor in accordance with this exemplary embodiment is increased by suppressing occurrence of image density unevenness even in the end portions of the photoreceptor. Therefore, the percentage of the length of the effective region based on the length of the cylindrical support at the axial direction may be 92% or more, and even furthermore 95% or more.
As shown in
From the viewpoint of the necessity for a region for attaching a jig required for arranging the photoreceptor in an image-forming apparatus, an region Q at which the layer is not formed is preferably provided between the end B of the charge-generating layer and the end C of the cylindrical support. When the charge-generating layer and the charge-transporting layer are formed by dip coating, a formed coating extends to the end of the base material (the cylindrical support), and thus a coating formed on the jig-attaching region is wiped off.
As shown in
The thickness of the charge-generating layer is preferably from 0.1 to 5 μm on average, and more preferably from 0.2 to 2.0 μm.
The thickness of the charge-generating layer at the both end portions A1 and A2 is preferably from 101% to 120%, more preferably from 105% to 115%, and even more preferably from 110 to 115%, with regard to the thickness of the charge-generating layer at the central portion O.
The undulation of thickness of the charge-generating layer in the circumferential direction and in the axial direction is preferably 10% or less, more preferably 8.5% or less, and still more preferably 5% or less, with regard to average film thickness of the generating layer. As a result, the irregularity of sensitivity of the photoreceptor as a whole may be prevented.
As used herein, “undulation” refers to surface unevenness generated in a minute space on the surface of a sample evaluated, and undulation at a certain point on the axis is defined as the maximum-minimum between the layer thickness at that point and the layer thickness measured at points ±5 mm from that point in the axial direction. In this exemplary embodiment, the thickness at a certain point on the axis is the average thickness at 24 points at 15° intervals (relative to that point) in the circumferential direction. In this exemplary embodiment, the difference in thickness of the layer is preferably in the above range relative to the average layer thickness.
The spectroscopic absorption ratio (spectroscopic absorption ratio determined for a sample containing not only the charge-generating layer but also other layers such as the charge-transporting layer) of the photoreceptor in this exemplary embodiment is preferably decreased from the central portion in the directions towards the both end portions in the axial direction of the photoreceptor, and the difference in spectroscopic absorption ratio between the two end portions is preferably 3.0% or less, and more preferably 2.5% or less, with regard to the spectroscopic absorption ratio at the central portion. As described above, the thickness of the charge-generating layer may be expressed in terms of spectroscopic absorption ratio, and thus the definition of the photoreceptor in this exemplary embodiment in terms of spectroscopic absorption ratio before calculation of layer thickness is a direct method and is extremely useful in quality control.
The spectroscopic absorption ratio at the end portions A1 and A2 is preferably 75 to 99%, more preferably 75 to 95%, and still more preferably 75 to 90% respectively, with regard to the spectroscopic absorption ratio at the central portion O in the axial direction.
The charge-generating layer according to this exemplary embodiment has the layer thickness distribution described above, and thus the charge-generating layer is preferably formed by an inkjet method.
In a jetting system in the inkjet method, a general system such as a continuous or intermittent type (for example, piezoelectric, thermal or electrostatic type) may be used, among them, a piezoelectric continuous or intermittent type is preferable, and a piezoelectric intermittent type is more preferable.
As shown in
As described above, since it is difficult to decrease the distance between nozzles and thus difficult to increase the resolution in the piezoelectric ink jet droplet discharge head, it is preferable that, in consideration of the distance between arranged nozzles, the droplet discharge head is arranged to be inclined relative to the axis of the photoreceptor as shown in
In this state, the cylindrical support is rotated and simultaneously a coating solution is jetted through the nozzles, and as shown in
Specifically, the cylindrical support is fit to a device capable of horizontally rotating, and the droplet discharge head charged with a charge-generating layer coating solution is arranged so as to jet droplets onto the cylindrical support. Because the object onto which droplets are jetted is a cylinder having a small diameter, nozzles through which the coating solution will not reach the cylinder are preferably closed, from the viewpoint of reducing the amount of waste liquid.
Here, a cylindrical coating base material is shown, but a flat coating base material may also be used if the base material and the droplet discharge head can be relatively moved.
In
In
By using the droplet discharge head, a coating film having the film thickness distribution of the charge-generating layer at both the end portions A1 and A2of the base material in the axial direction is formed.
In the scanning systems shown in
For example, when the continuous droplet discharge head is used, the direction along which droplets are discharged may be changed with a bias in an electric field such that some droplets will not reach the base material, particularly in a thin-film region at the central portion of the base material. Droplets not used in forming a coating film are recovered through a gutter.
In the intermittent type, it is preferable that the discharge frequency is increased at the end portions A1 and A2. It is also preferable that the amount of discharge is increased by increasing a pulse voltage or by increasing the time. Nozzles not jetting droplets onto a thin-film forming part by giving no pulse may also be arranged.
In the droplet discharge head shown in
For the intermittent ink jet droplet discharge head, a viscosity of a coating solution is preferably in a range of from 0.8 mPa·s to 20 mPa·s, and more preferably in a range of from 1 Pa·s to 10 mPa·s.
The viscosity in this exemplary embodiment refers to a value determined by an E-type viscometer (RE550L, standard cone rotor, revolution rate of 60 rpm, manufactured by Toki Sangyo Co., Ltd.) at 25° C.
For adjusting the viscosity of the coating solution, the above-described charge-generating material, resin and other additives such as particles are preferably contained in solvent. Any ordinary organic solvent may be used, including, for example, methanol, ethanol, n-propanol, n-butanol, benzyl alcohol, methyl cellosolve, ethyl cellosolve, 3-hydroxy-3-methyl-2-butanone, diacetone alcohol, γ-ketobutanol, acetol, butyl carbitol, glycerin, acetone, methyl ethyl ketone, cyclohexanone, methyl acetate, n-butyl acetate, dioxane, tetrahydrofuran, methylene chloride, chloroform, chlorobenzene, and toluene. These solvents may be used alone or in combination of two or more thereof.
When a coating solution at high concentration, that is, a coating solution of high viscosity is used for the purpose of reducing the amount of solvent released into the air, the continuous ink jet droplet discharge head for pressurizing the coating solution is preferable. However, even an intermittent head may also be used for a highly viscous material by providing it with a heater to heat a coating solution used in a commercial bar coat printer to reduce viscosity at jetting portions. Although a kind of coating solutions selected is limited, an electrostatic intermittent ink jet droplet discharge head may cope with a highly viscous coating solution.
The diameter of droplet to be jetted is preferably from 1 pl to 60 pl, more preferably from 1.5 pl to 55 pl, and still more preferably from 2.0 pl to 50 pl. The droplet in this range hardly generates clogging of nozzles and is also preferable from the viewpoint of productivity. Further, the concentration of droplets reaching the surface of the object may also be easily regulated.
In this exemplary embodiment, the diameter of droplets is determined by off-line visualization evaluation. Droplets are lighted by LED in synchronization with jetting timing and their image is observed with a CCD camera.
The method of forming the layer by the ink jet method has been described by reference to the method of forming the charge-generating layer, but this ink jet method may also be used in formation of other layers such as a charge-transporting layer.
<Electrophotographic Photoreceptor>
In
Next, layers other than the charge-generating layer constituting the electrophotographic photoreceptor are described.
(Cylindrical Support 4)
In this exemplary embodiment, a cylindrical support 4 is used as base material.
The cylindrical support 4 may be, for example, a metal plate, a metal drum or a metal belt formed of a metal such as aluminum, copper, zinc, stainless steel, chromium, nickel, molybdenum, vanadium, indium, gold or platinum, or their alloy, as well as paper, plastic films or belts coated, deposited or laminated with a polymer with a volume resistivity of 10−5 Ω·cm or less or indium oxide or with a metal such as aluminum, palladium or gold or their alloy.
The volume resistivity of the cylindrical support is preferably 10−5 Ω·cm or less.
The surface of the cylindrical support 4 may be roughened so that the central line average surface roughness Ra of the support is preferably from 0.04 μm to 0.5 μm in order to prevent interference-preventing effect generated upon irradiation with a laser light.
For roughening the surface of the support, for example, employable is a wet-honing method of jetting an abrasive suspension in water to a support; a centerless grinding method of pressing a support against a rotating grindstone for continuously grinding it; or a method of anodic oxidation, and it is also preferable to use a method wherein a layer in which a powder having a volume resistivity of 10−5 Ω·cm or less is dispersed in a resin layer is formed on the surface of the support without roughened, and the surface is roughed by the particles dispersed in the layer.
When non-interference light is used as a light source, roughening for prevention of interference pattern is not particularly necessary.
As one method of roughening the surface of the support, the anodic oxidation comprises processing the aluminum surface of a support in an electrolytic solution in which the aluminum acts as an anode for anodic oxidation to form an oxide film on the aluminum surface. The electrolytic solution includes sulfuric acid solution and oxalic acid solution. Preferably, the thickness of the oxide film by anodic oxidation is preferably from 0.3 to 15 μm for sealing the fine pores thereof.
The treatment with an acid solution, such as phosphoric acid, chromic acid and hydrofluoric acid, may be effected as follows. The blend ratio of phosphoric acid, chromic acid and hydrofluoric acid to form an acid solution is preferably as follows: Phosphoric acid is from 10 wt % to 11 wt %, chromic acid is from 3 wt % to 5 wt %, and hydrofluoric acid is from 0.5 wt % to 2 wt %. The total acid concentration of these is preferably from 13.5 wt % to 18 wt %. The processing temperature is preferably from 42° C. to 48° C.
Preferably, the thickness of the film is from 0.3 μm to 15 μm.
The boehmite treatment may be attained by dipping the support in pure water at 90 to 100° C. for 5 to 60 minutes, or by contacting the support with heated steam at 90 to 120° C. for 5 to 60 minutes. Preferably, the thickness of the film is from 0.1 to 5 μm. This may be further processed for anodic oxidation with an electrolytic solution having low film dissolution ability, such as a solution of adipic acid, boric acid, borate, phosphate, phthalate, maleate, benzoate, tartrate or citrate.
(Undercoat Layer 1)
An undercoat layer 1 may also be formed on the cylindrical support, or between the layer formed on the cylindrical support and the photosensitive layer. Particularly, the undercoat layer 1 that is an intermediate layer is preferably formed.
The material used in forming the undercoat layer 1 includes organozirconium compounds such as zirconium chelate compound, zirconium alkoxide compound and zirconium coupling agent; organotitanium compounds such as titanium chelate compound, titanium alkoxide compound and titanate coupling agent; organoaluminum compounds such as aluminum chelate compound and aluminum coupling agent; or organometallic compounds such as antimony alkoxide compound, germanium alkoxide compound, indium alkoxide compound, indium chelate compound, manganese alkoxide compound, manganese chelate compound, tin alkoxide compound, tin chelate compound, aluminum silicon alkoxide compound, aluminum titanium alkoxide compound and aluminum zirconium alkoxide compound, among which the organozirconium compounds, organotitanium compounds or organoaluminum compounds are particularly preferably used.
Further, silane coupling agents such vinyl trichlorosilane, vinyl trimethoxy silane, vinyl triethoxy silane, vinyl tris-2-methoxy ethoxy silane, vinyl triacetoxy silane, γ-glycidoxy propyl trimethoxy silane, γ-methacryloxy propyl trimethoxy silane, γ-aminopropyl triethoxy silane, γ-chloropropyl trimethoxy silane, γ-2-aminoethyl aminopropyl trimethoxy silane, γ-mercaptopropyl trimethoxy silane, γ-ureidopropyl triethoxy silane and β-3,4-epoxy cyclohexyl trimethoxy silane may be used in the undercoat layer.
As another constituent component generally used in the undercoat layer 1, it is also possible to use known binder resins, for example polyvinyl alcohol, polyvinyl methyl ether, poly-N-vinylimidazole, polyethylene oxide, ethyl cellulose, methyl cellulose, ethylene-acrylic acid copolymer, polyamide, polyimide, casein, gelatin, polyethylene, polyester, phenol resin, vinyl chloride-vinyl acetate copolymer, epoxy resin, polyvinyl pyrrolidone, polyvinyl pyridine, polyurethane, polyglutamic acid and polyacrylic acid.
The resin may be used alone or in combination of two or more thereof, and the mixing ratio of these materials may be suitably established depending on necessity.
An electron transportable pigment may be mixed or dispersed in the undercoat layer 1. The electron transportable pigment include organic pigments such as perylene pigment described in JP-A No. 47-30330, bisbenzimidazole perylene pigment, polycyclic quinone pigment, indigo pigment and quinacridone pigment; organic pigments such as bisazo pigment and phthalocyanine pigment having an electron attractive substituent group such as a cyano group, a nitro group, a nitroso group and a halogen atom; and inorganic pigments such as zinc oxide and titanium oxide.
Among these pigments, perylene pigment, bisbenzimidazole perylene pigment, polycyclic quinone pigment, zinc oxide and titanium oxide are preferably used.
The surfaces of these pigments may be treated with the above-mentioned coupling agent, binder or the like for the purpose of regulating dispersibility or charge transportability. The electron transportable pigment is used in an amount of 95 wt % or less, and preferably 90 wt % or less.
As the method of mixing/dispersing the constituent component of the undercoat layer 1, a usual method of using a ball mill, a roll mill, a sand mill, an atrighter or supersonic waves is used. Mixing/dispersion is carried out in an organic solvent. The organic solvent may be any organic solvent, as long as the organic solvent dissolves an organic metallic compound and resin and don't cause gelation or aggregation upon mixing/dispersion of the electron transportable pigment.
For example, the organic solvent includes a usual organic solvent such as methanol, ethanol, n-propanol, n-butanol, benzyl alcohol, methyl Cellosolve, ethyl Cellosolve, acetone, methyl ethyl ketone, cyclohexanone, methyl acetate, n-butyl acetate, dioxane, tetrahydrofuran, methylene chloride, chloroform, chlorobenzene and toluene. The organic solvent may be used alone or in combination of two or more thereof.
Various organic compound powder or inorganic compound powder may be added to the undercoat layer 1 for the purpose of improving the electric properties and the light-scatterability of the layer. In particular, white pigments such as titanium oxide, zinc oxide, zinc white, zinc sulfide, lead white or lithopone; inorganic pigments as body pigments such as alumina, calcium carbonate or barium sulfate; Teflon (trade name) resin particles, benzoguanamine resin particles or styrene particles are effective.
Preferably, the particle size of the additive powder is preferably from 0.01 to 2 μm in terms of volume-average particle diameter. The additive powder is optionally added to the layer. When the additive powder is added, its amount is preferably from 10 to 90 wt %, and more preferably from 30 to 80 wt %, with regard to the total solid content of the undercoat layer 1.
Incorporation of an electron-transporting substance, an electron-transporting pigment etc. into the undercoat layer 1 is also effective.
The thickness of the undercoat layer 1 is preferably from 0.01 μm to 30 μm, and more preferably from 0.05 μm to 25 μm. A powdery substance, when added in preparing a coating solution for forming the undercoat layer 1, is added to and dispersed in a solution of the resin component.
As a dispersing method, any ordinary method may be employed by using, for example, a roll mill, a ball mill, a vibrating ball mill, an attritor, a sand mill, a colloid mill, or a paint shaker. The undercoat layer 1 may be formed by applying a coating solution for forming the undercoat layer 1 on or above the cylindrical support 4 and drying it.
The coating method may be any ordinary one, including, for example, a blade coating method, a wire bar coating method, a spraying method, a dipping method, a bead coating method, an air knife coating method and a curtain coating method.
(Charge-Transporting Layer 3)
The charge-transporting layer 3 will be described in detail.
As the charge-transporting layer 3, a layer formed by known techniques may be used. The charge-transporting layer 3 may be formed by using a charge transport material and resin or by using a polymer charge transport material.
The charge transport material includes electron transport compounds, for example quinone compounds such as p-benzoquinone, chloranil, bromanil or anthraquinone; tetracyanoquinodimethane compound; fluorenone compound such as 2,4,7-trinitrofluorenone; xanthone compound; benzophenone compound; cyanovinyl compound and ethylene compound. The charge transport material includes hole transport compounds such as triaryl amine compound, benzidine compound, aryl alkane compound, aryl-substituted ethylene compound, stilbene compound, anthracene compound and hydrazone compound.
These charge transport materials may be used alone or in combination of two or more thereof, and the charge transport material is not limited thereto. These charge transport materials are preferably those having structures represented by the following formulae:
wherein R14 represents a hydrogen atom or a methyl group; n indicates 1 or 2; Ar6 and Ar7 each independently represent a substituted or unsubstituted aryl group, —C6H4—C(R18)═C(R19)(R20) or —C6H4—CH═CH—CH═C(Ar)2, and the substituent for these is a halogen atom, an alkyl group having from 1 to 5 carbon atoms, an alkoxy group having from 1 to 5 carbon atoms, or a substituted amino group substituted with an alkyl group having from 1 to 3 carbon atoms; Ar represents a substituted or unsubstituted aryl group; and R18, R19 and R20 each independently represent a hydrogen atom, a substituted or unsubstituted alkyl group, or a substituted or unsubstituted aryl group.
In the above formula, R15 and R15, may be the same or different, and each independently represent a hydrogen atom, a halogen atom, an alkyl group having from 1 to 5 carbon atoms, or an alkoxy group having from 1 to 5 carbon atoms; R16, R16,, R17 and R17, may be the same or different, and each independently represent a hydrogen atom, a halogen atom, an alkyl group having from 1 to 5 carbon atoms, an alkoxy group having from 1 to 5 carbon atoms, an amino group substituted with an alkyl group having 1 or 2 carbon atoms, a substituted or unsubstituted aryl group, —C(R18)═C(R19)(R20), or —CH═CH—CH═C(Ar)2; R18, R19 and R20 each independently represent a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group; Ar represents a substituted or unsubstituted aryl group; and each of m and n each independently represent an integer of from 0 to 2.
In the formula, R21 represents a hydrogen atom, an alkyl group having from 1 to 5 carbon atoms, an alkoxy group having from 1 to 5 carbon atoms, a substituted or unsubstituted aryl group, or —CH═CH—CH═C(Ar)2; Ar represents a substituted or unsubstituted aryl group; R22 and R23 may be the same or different and each independently represent a hydrogen atom, a halogen atom, an alkyl group having from 1 to 5 carbon atoms, an alkoxy group having from 1 to 5 carbon atoms, an amino group substituted with an alkyl group having 1 or 2 carbon atoms, or a substituted or unsubstituted aryl group.
The binder resin used in the charge-transporting layer 3 includes polycarbonate resin, polyester resin, methacryl resin, acryl resin, polyvinyl chloride resin, polyvinylidene chloride resin, polystyrene resin, polyvinyl acetate resin, styrene-butadiene copolymer, vinylidene chloride-acrylonitrile copolymer, vinyl chloride-vinyl acetate copolymer, vinyl chloride-vinyl acetate-maleic anhydride copolymer, silicon resin, silicon-alkyd resin, phenol-formaldehyde resin, styrene-alkyd resin, polymer charge transport materials such as poly-N-vinyl carbazole, polysilane, polyesteric polymer charge transport materials described in JP-A No. 8-176293 and JP-A No. 8-208820. These binder resins may be used alone or in combination of two or more thereof.
The compounding ratio (weight ratio) of the charge transport material to the resin is preferably from 10:1 to 1:5.
The polymer charge transport materials may be used alone.
As the polymer charge transport materials, known materials having charge transportability, such as poly-N-vinyl carbazole and polysilane, may be used. Particularly polyesteric polymer charge transport materials described in JP-A No. 8-176293 and JP-A No. 8-208820 are particularly preferable. The polymer charge transport material only may be used as the charge-transporting layer 3, or in combination with the resin to form a coating.
The thickness of the charge-transporting layer 3 is generally from 5 μm to 50 μm, and preferably from 10 μm to 30 μm.
The coating method includes a usual method such as blade coating, Meyer bar coating, spray coating, dip coating, bead coating, air knife coating and curtain coating.
The solvent used in arranging the charge-transporting layer 3 includes usual organic solvents such as aromatic hydrocarbons such as benzene, toluene, xylene or chlorobenzene; ketones such as acetone or 2-butanone; halogenated aliphatic hydrocarbons such as methylene chloride, chloroform or ethylene chloride; or cyclic or linear ethers such as tetrahydrofuran or ethyl ether. These solvent may be used alone or in combination of two or more thereof.
For the purpose of preventing the deterioration of the photoreceptor by ozone and an oxidizing gas generated in a copier or by light or heat, additives such as an antioxidant, a light stabilizer and a heat stabilizer may be added to the photosensitive layer.
For example, the antioxidant includes hindered phenol, hindered amine, paraphenylene diamine, aryl alkane, hydroquinone, spirochroman, spiroindanone and derivatives thereof, organic sulfur compounds, organic phosphorous compounds or the like. Examples of the light stabilizer include derivatives such as benzophenone, benzotriazole, dithiocarbamate or tetramethyl piperidine.
For the purpose of improvement in sensitivity, reduction in residual potential, reduction in fatigue upon repeated use, etc., at least one kind of electron receptor may be contained. The electron receptor usable in the photoreceptor includes, for example, succinicanhydride, maleicanhydride, dibromomaleicanhydride, phthalicanhydride, tetrabromophthalicanhydride, tetracyanoethylene, tetracyanoquinodimethane, o-dinitrobenzene, m-dinitrobenzene, chloranil, dinitroanthraquinone, trinitrofluorenone, picric acid, o-nitrobenzoic acid, p-nitrobenzoic acid and phthalic. Among these compounds, benzene derivatives having electron attractive substituent groups such as a fluorenonic group, a quinonic group, Cl, CN or NO2 are particularly preferable.
(Protective Layer 5)
The protective layer (layer constituting the outermost layer) 5 will be described in detail.
To confer resistance with respect to abrasion, scratch or the like on the surface of the protective layer, a high-strength protective layer may also be arranged. This high-strength protective layer is preferably a layer wherein particles with volume resistivity of 107 Ω·cm or less are dispersed in a resin, or lubricating particles such as a fluorine resin, an acryl resin or the like are dispersed in a usual charge-transporting layer material, or a hard coating such as silicon and acryl is used, and the protective layer preferably has a crosslinked structure, and more preferably a charge transport material.
The resin may be either thermosetting or photosetting (including UV-setting).
Specific examples of the resin include phenol resin, epoxy resin, urethane resin, urea resin, siloxane resin or the like, among which a resin having a phenol structure having a charge transportability, such as novolak-based phenol resin, resol-based phenol resin, or epoxy resin having a phenol structure is preferable, and a phenol derivative having at least a methylol group, such as resol-based phenol resin, is more preferable.
The phenol derivatives having a methylol group include monomers of monomethylolphenols, dimethylolphenols or trimethylolphenols, mixtures thereor, oligomers thereof, or mixtures of such monomers and oligomers, which are produced through reaction of phenol structure-containing compounds such as resorcinols or bisphenols with formaldehyde or paraformaldehyde, in the presence of an acid catalyst or an alkali catalyst. The phenol structure-containing compounds include substituted phenols having one hydroxyl group such as phenol, cresol, xylenol, paraalphenol or paraphenryphenol; substituted phenols having two hydroxyl groups such as catechol, resorcinol or hydroquinone; bisphenols or biphenols such as bisphenol A or bisphenol Z. Of the compounds, moleculars having from about 2 to 20 repeating units are referred to as oligomers, and those smaller than such oligomers are referred to as monomers.
The acid catalyst includes, for example, sulfuric acid, paratoluenesulfonic acid or phosphoric acid. The alkali catalyst includes, for example, alkali metal or alkaline earth metal hydroxides such as NaOH, KOH ord Ca(OH)2; or amine catalysts. The amine catalysts include, but are not limited to, ammonia, hexamethylenetetramine, triethylamine, triethylamine, and triethanolamine. When a basic catalyst is used, it is neutralized with an acid, or it is inactivated through contact with an adsorbent such as silica gel or with ion-exchange resin. A catalyst for promoting the curing may be used when a coating solution is prepared. At the time of curing, the catalyst may also be used, and the amount of the catalyst added is preferably 5 wt % or less.
As materials forming a crosslinked structure, various compounds may be used, and from the viewpoint of characteristics, phenol resin, urethane resin and siloxane resin are preferable, and particularly siloxane resin and phenol resin are preferable.
The charge-transporting material may be any may be any charge-transporting material as long as a substance has a charge transporting ability, and may be low-molecular compounds excellent in a charge transporting ability such as hydrazone-based compounds, benzidine-based compounds, amine-based compounds or stilbene-based compounds, and preferably those having a structure capable of crosslinking reaction.
The charge transporting materials capable of crosslinking reaction includes those represented by the following Formulae (I) to (V), and for example, specific structures shown below may be used.
F—(X1)n—R1-A)m Formula (I):
In the formula (I), F represents an organic group derived from a compound having an ability to transport an electron hole, R1 represents an alkylene group, m represents an integer of from 1 to 4, X1 represents oxygen or sulfur, n represents 0 or 1, and A represents a hydroxyl group, a carboxyl group or a thiol group.
F—[(X2)n1-(R2)n2-(Z2)n3-G]n4 Formula (II):
In the Formula (II), F represents an organic group derived from a compound having an ability to transport an electron hole, X2 represents an oxygen atom or a sulfur atom, R2 represents an alkylene group, Z2 represents an alkylene group, an oxygen atom, a sulfur atom, NH or COO, G represents an epoxy group, n1, n2 and n3 each independently represent 0 or 1, and n4 represents an integer of 1 to 4.
In the Formula (III), F represents an n5-valent organic group having an ability to transport an electron hole, T represents a divalent group, Y represents an oxygen atom or a sulfur atom, R3, R4 and R5 each independently represent a hydrogen atom or a monovalent organic group, R6 represent a monovalent organic group, m1 represents 0 or 1, and n5 represents an integer of 1 to 4, provided that R5 and R6 may be bound to each other to form a heterocyclic ring having Y as heteroatom.
In the Formula (IV), F represents an n6-valent organic group having an ability to transport an electron hole, T2 represents a divalent group, R7 represents a monovalent organic group, m2 represents 0 or 1, and n6 represents an integer of from 1 to 4.
In the Formula (V), F represents an n7-valent organic group having an ability to transport an electron hole, T3 represents a divalent alkylene group, R0 represents a monovalent organic group, and n7 represents an integer of from 1 to 4.
For the purpose of regulating the film formation, flexibility, lubricating properties or adhesion of the protective layer 5, other coupling agents or fluorine compounds may be mixed. As these compounds, various silane coupling agents and commercial silicone-based hard coating agents may be available.
Silane coupling agents include, for example, vinyl trichlorosilane, vinyl trimethoxy silane, vinyl triethoxy silane, γ-glycidoxy propyl methyl diethoxy silane, γ-glycidoxy propyl trimethoxy silane, γ-glycidoxy propyl trimethoxy silane, γ-aminopropyl triethoxy silane, γ-aminopropyl trimethoxy silane, γ-aminopropyl methyl dimethoxy silane, N-β(aminoethyl) γ-aminopropyl triethoxy silane, tetramethoxy silane, methyl trimethoxy silane, dimethyl dimethoxy silane, or the like.
The commercial hard coating agents include, for example, KP-85, X-40-9740, X-40-2239 (manufactured by Shin-Etsu Chemical Co., Ltd), AY42-440, AY42-441 or AY49-208 (manufactured by Dow Coming Toray). For conferring water repellency etc., fluorine-containing compounds such as (tridecafluoro-1,1,2,2-tetrahydrooctyl) triethoxy silane, (3,3,3-trifluoropropyl) trimethoxy silane, 3-(heptafluoroisopropoxy) propyl triethoxy silane, 1H,1H,2H,2H-perfluoroalkyl triethoxy silane, 1H,1H,2H,2H-perfluorodecyl triethoxy silane and 1H,1H,2H,2H-perfluoroctyl triethoxy silane may be added.
The silane coupling agent may be used in any amount. The amount of the fluorine-containing compound is desirably in an amount of 0.25 part by weight or less with regard to the fluorine-free compound.
A resin soluble in an alcohol may also be added to the protective layer 5.
The alcohol-soluble resin includes, for example, polyvinyl butyral resin, polyvinyl formal resin, polyvinyl acetal resin such as partially acetalated polyvinyl acetal resin having a part of butyral modified with formal, acetoacetal or the like (for example, S-LEC B, K etc. manufactured by Sekisui Chemical Co., Ltd.), polyamide resin, cellulose resin, polyvinyl phenol resin or the like. Particularly, polyvinyl acetal resin or polyvinyl phenol resin are preferable.
The weight-average molecular weight of the resin is preferably from 2,000 to 100,000, and more preferably from 5,000 to 50,000.
The amount of the resin added is preferably from 1 wt % to 20 wt %, more preferably from 1 wt % to 15 wt %, and still more preferably 2 wt % to 10 wt %, with regard to the total solid content of the protective layer 5.
The coating solution for protective layer 5 containing these components may also be produced in the absence of a solvent, but if necessary it is possible to use solvents, for example, alcohols such as methanol, ethanol, propanol or butanol; ketones such as acetone, methyl ethyl ketone or cyclohexanone; ethers such as tetrahydrofuran diethyl ether or dioxane, or the like. These solvents may be use alone or in combination of two or more thereof. Such solvents preferably have a boiling point of 120° C. or less. The amount of the solvent may be regulated.
When the above components are reacted to obtain a coating solution, they may be simply mixed and dissolved, or may be additionally heated at from 20° C. to 100° C., and preferably from 30° C. to 80° C., for 10 minutes to 100 hours, and preferably for 1 hour to 50 hours. Sonication of the mixture is also preferable. By doing so, partial reaction is estimated to proceed to improve coating property.
An antioxidant is preferably added to the protective layer 5.
The antioxidant is preferably a hindered phenol- or hindered amine-based antioxidant, and known antioxidants such as an organic sulfur-based antioxidant, phosphite-based antioxidant, dithiocarbamate-based antioxidant, thiourea-based antioxidant and benzoimidazole-based antioxidant may also be used. The amount of the antioxidant added is preferably 20 wt % or less, and more preferably 10 wt % or less.
The hindered phenolic antioxidants include, for example,
Various particles may be added to the protective layer 5. By way of example, silicon-containing particles may be mentioned as the particles. The silicon-containing particles are those containing a silicon atom as the constitutive element. Concretely, they include colloidal silica or silicone particles.
Preferably, the colloidal silica as the silicon-containing particles preferably has a mean particle size of from 1 nm to 100 nm, more preferably from 10 nm to 30 nm. It may be an acid or alkaline aqueous dispersion, or a dispersion in an organic solvent such as alcohol, ketone or ester. Ordinary commercial products of such colloidal silica are usable herein.
Though not specifically restricted, the solid content of the colloidal silica in the protective layer 5 is preferably from 0.1 wt % to 50 wt %, and more preferably from 0.1 wt % to 30 wt % with regard to the total solid content of the protective layer 5 in view of the film-formability, the electric properties or the strength of the layer.
The silicone particles used as the silicon-containing particles are selected from silicone resin particles, silicone rubber particles, and silica particles surface-treated with silicone. Ordinary commercial products of such silicone particles are usable herein. These silicone particles are spherical particles preferably having a mean particle size of from 1 nm to 500 nm, and more preferably from 10 nm to 100 nm.
The content of the silicone particles in the protective layer 5 is preferably from 0.1 wt % to 30 wt %, and more preferably from 0.5 wt % to 10 wt % with regard to the total solid content of the protective layer 5.
Examples of other particles are fluorine-containing particles of ethylene tetrafluoride, ethylene trifluoride, propylene hexafluoride, vinyl fluoride or vinylidene fluoride; resin particles of a copolymer of fluororesin and hydroxyl group-containing monomer discribed in Preprint for 8th Polymer Material Forum Meeting, p. 89; and metal oxides such as ZnO—Al2O3, SnO2—Sb2O3, In2O3—SnO2, ZnO2—TiO2, ZnO—TiO2, MgO—Al2O3, FeO—TiO2, TiO2, SnO2, In2O3, ZnO or MgO.
Oil such as silicone oil may also be added to the layer. The silicone oil includes, for example, silicone oils such as dimethylpolysiloxane, diphenylpolysiloxane or phenylmethylsiloxane; reactive silicone oils such as amino-modified polysiloxanes, epoxy-modified polysiloxanes, carboxyl-modified polysiloxanes, carbinol-modified polysiloxanes, methacryl-modified polysiloxanes, mercapto-modified polysiloxanes and phenol-modified polysiloxanes; dimethyl cyclosiloxane such as hexamethyl cyclotrisiloxane, octamethyl cyclotetrasiloxane, decamethyl cyclopentasiloane and dodecamethyl cyclohexasiloxane, methyl phenyl cyclosiloxanes such as 1,3,5-trimethyl-1,3,5-triphenyl cyclotrisiloxane, 1,3,5,7-tetramethyl-1,3,5,7-tetraphenyl cyclotetrasiloxane, or 1,3,5,7,9-pentamethyl-1,3,5,7,9-pentaphenyl cyclopentasiloxane; phenyl cyclosiloxane such as hexaphenyl cyclotrisiloxane; fluorine-containing cyclosiloxanes such as 3-(3,3,3-trifluoropropyl)methyl cyclotrisiloxane; a methyl hydroxy siloxane mixture, hydrosilyl group-containing cyclosiloxane such as pentamethyl cyclopentasiloxane or phenyl hydrocyclosiloxane; and vinyl group-containing cyclosiloxane such as pentavinyl pentamethyl cyclopentasiloxane. These compounds may be used alone or in combination of two or more thereof. When the compounds are used in combination, they may be simply mixed or may be prepared in the form of a solid solution or in a fused form.
The average particle diameter of the particles is preferably 0.3 μm or less, and more preferably 0.1 μm or less, from the viewpoint of the transparency of the protective layer.
<Image-Forming Apparatus>
The cleaner 27 have a fibrous member (roll) 27a and a cleaning blade (blade member) 27b. In the cleaner 27 shown in
The cleaning blade and the cleaning brush of the cleaner 27 remove the adhered substances (e.g., discharged substances) from the surface of the photoreceptor, and it is desirable that a lubricant substance (lubricant component) 14 such as metal soap, higher alcohol, wax or silicone oil is contacted with the fibrous member 27a, to supply the lubricant component to the surface of the electrophotographic photoreceptor.
The cleaning blade 27b may be an ordinary rubber blade.
The process cartridge 20 described above is detachably fitted to the main body of the image-forming apparatus, and constitutes the image-forming apparatus, together with the main body of the image-forming apparatus.
The exposure unit 30 may be any one capable of exposing the charged electrophotographic photoreceptor 10 so as to form an electrostatic latent image thereon. The light source of the exposure unit 30 is preferably a multi-beam surface-emitting laser.
The transfer unit 40 is not limited insofar as it may transfer a toner image on the electrophotographic photoreceptor 10 onto a transfer medium (which may be a paper retained on a paper delivery belt (not shown) used in place of the intermediate transfer medium 50 as transfer medium shown in
The intermediate transfer medium 50 has a volume resistivity of 102 Ω·cm to 1011 Ω·cm, and is a belt-shaped medium (intermediate transfer belt) containing polyimide, polyamidimide, polycarbonate, polyarylate, polyester, rubber or the like as the constituent component. The intermediate transfer medium 50 may be in the form of a drum in addition to the form of a belt.
The transfer medium is not particularly limited insofar as it is a medium capable of transferring a toner image formed on the electrophotographic photoreceptor 10. For example, in the case where the electrophotographic photoreceptor 10 is transferred directly onto a paper, the paper is a transfer medium, and when the intermediate transfer medium 50 is used, the intermediate transfer medium is a transfer medium.
In the image-forming apparatus 110, the electrophotographic photoreceptor 10 and the other units are separated from one another, and the charger 22, the developer 25 and the cleaner 27 may be detachably fitted to the body of the image-forming apparatus by leading or extrusion.
In the electrophotographic photoreceptor of this exemplary embodiment, formation of the cartridge is not necessary in some cases. Accordingly, the charger 22, the developer 25 and the cleaner 27 may be detachably fitted to the body of the image-forming apparatus by leading or extrusion, whereby the apparatus cost per one print with it may be reduced. Two or more of these units may be manufactured as one integrated cartridge to detachably fix to the body.
The image-forming apparatus 110 has the same structure as the image-forming apparatus 100 except that the charger 22, the developer 25 and the cleaner 27 are formed as cartridges respectively.
Hereinafter, the exemplary embodiment of the present invention is described in more detail with reference to the Examples, to which, however, the present invention is not limited.
<Preparation of Photoreceptor>
A cylindrical aluminum support has outer diameter of 30 mm and length of 253 mm. The outer periphery of the cylindrical aluminum support is polished with a centerless polishing apparatus to give a cylinder having a surface roughness (ten-point average roughness) Rz of 0.6 μm. This cylinder is degreased, and then etched with an aqueous 2 wt % sodium hydroxide solution for 1 minute, successively neutralized and washed with pure water.
Next, this aluminum support is subjected to anodic oxidation with a 10 wt % sulfuric acid solution (current density, 1.0 A/dm2) to thereby form an oxide film on its surface. After washed with water, the support is dipped in a 1 wt % nickel acetate solution at 80° C. for 20 minutes for sealing the anodic oxide film. Further, the support is washed with pure water and dried. In this manner, a cylindrical support having a 7-μm anoxic oxide film formed on the outer periphery thereof is obtained.
Subsequently, 2.5 parts by weight of gallium phthalocyanine chloride having diffraction peak at least at a Bragg angle (2θ±0.2°) of 7.4°, 16.6°, 25.5° and 28.3° on X-ray diffraction spectrum, 2.5 parts by weight of polyvinylbutyral (S-LEC BM-S, by Sekisui Chemical Co., Ltd.) and n-butyl acetate are mixed, and dispersed in a paint shaker along with glass beads therein for 1 hour, followed by removing the glass beads to give a charge-generating layer-forming coating solution having a solid content of 5 wt % and a viscosity of 5.0 mPa·s.
As shown in
The reason why the position 12 mm from the end X1 is set as the position Y1 for initiation of coating is because the sensitivity of the photoreceptor is measured under conditions where the thickness of the charge-transporting layer is not varied in the axial direction. When the charge-transporting layer is formed on the charge-generating layer, the charge-transporting layer is thicker than the charge-generating layer, whereby the coating film easily drips, and the ends in the axial direction tend to be different in layer thickness. That is, a broad region not coated with the charge-generating layer is provided from X1 to Y1 and from X2 to Y2 so that the thickness of the charge-transporting layer becomes constant in the coating region from Y1 to Y2 of the charge-generating layer.
In this example, because of coating starts at Y1, the position located 2 mm toward the central portion from Y1 is the end portion Z1. However, application of the coating solution for charge-generating layer may start at X1, and in this case, the position located 2 mm toward the central portion from X1 is the end portion.
As the droplet discharge head for forming the charge-generating layer, a piezoelectric intermittent Pixel Jet 64 having 32 nozzles×2 arrays manufactured by Trident is used, and out of 64 nozzles in the droplet discharge head, 20 nozzles in one array are used. The droplet discharge head is arranged at an inclined angle of 85° to the axis of the cylindrical support, where the frequency of jetting of the coating solution is 2.5 kHz and the distance between the droplet discharge head and the cylindrical support is 1 mm.
After the axis of the cylindrical support is arranged horizontally, the cylindrical support is rotated at 200 rpm while the average scanning speed of the droplet discharge head in the axial direction is 261 mm/min., and the volume of droplet to be jetted is 50 pl, and droplets are applied onto the cylindrical support. The diameter of droplets is determined by off-line visualization evaluation. Droplets are lighted by LED in synchronization with jetting timing and their image is observed with a CCD camera.
As shown in
After the above procedure, the cylindrical support is heated at 100° C. for 10 minutes to form a charge-generating layer thereon.
Next, 2.5 parts by weight of a benzidine compound of the following formula (A-1), and 3 parts by weight of a polymer compound having structural units of the following formula (B-1) (having a viscosity-average molecular weight of 39,000) are dissolved in a mixed solvent of 5 parts by weight of chlorobenzene and 15 parts by weight of tetrahydrofuran to prepare a coating solution for forming a charge-transporting layer.
The cylindrical support 1 having the charge-generating layer formed thereon is coated by dipping with the coating solution for forming the charge-transporting layer. In this dip coating, the cylindrical support is dipped, to a position located 2 mm from the end X1 of the cylindrical support, in the coating solution for forming the charge-transporting layer. And then, the coating of charge-transporting layer starts by raising the cylindrical support, and finishes by completely raising the cylindrical support from the coating solution, whereby the coating solution is applied until the other end X2. Thereafter, the terminal region of 2 mm in width from the other end X2 is wiped out, and the support is heated at 120° C. for 40 minutes to form a charge-transporting layer of 20 μm in thickness to prepare photoreceptor-1.
Photoreceptor-2 is prepared in the same manner as in Example 1 except that in the preparation of the charge-generating layer in Example 1, the charge-generating layer is prepared by using the droplet discharge head and coating conditions shown in Table 2.
Photoreceptor-3 is prepared in the same manner as in Example 1 except that in the preparation of the charge-generating layer in Example 1, the charge-generating layer is prepared by using the coating solution and coating conditions shown in Table 2.
Regulation of the scanning speed (coating speed) of the droplet discharge head in the axial direction in Examples 2 and 3 is shown in
Photoreceptor-4 is prepared in the same manner as in Example 1 except that in the preparation of the charge-generating layer in Example 1, the charge-generating layer is prepared by using the droplet discharge head, the coating solution and coating conditions shown in Table 2.
Photoreceptor-5 is prepared in the same manner as in Example 1 except that while the charge-generating layer in Example 1 is prepared in an inkjet method, the charge-generating layer in Comparative Example 1 is prepared by a dip coating method with a dip coating apparatus.
The constitution of the dip coating apparatus used in Comparative Example 1 is shown in
Photoreceptor-6 is prepared in the same manner as in Comparative Example 1 except that while the cylindrical support is raised at a constant speed, the cylindrical support is raised at the coating speed shown in
<Evaluation>
(Film Thickness)
The film thickness distribution of the charge-generating layer is calculated by the spectroscopic absorption ratio of the charge-generating layer. The average film thickness of photoreceptor is measured between the positions Y1 and Y2 at 5-mm intervals in the axial direction at intervals of every 15° in the circumferential direction (that is, 24 points). The results are shown in
The results of film thickness distribution indicate that in Examples 1 and 3, the maximum thickness position, i.e. the position where the thickness of the charge-generating layer is the maximum, is a position located 2 mm toward the central portion from the position Y1 where coating is initiated, and in Example 2, the maximum thickness position is a position located 1.5 mm toward the central portion. In Comparative Example 1, on the other hand, the film thickness is gradually increased in the direction toward the lower side of the photoreceptor arranged in the vertical direction upon dip coating, and in Comparative Example 2, the maximum thickness position is a position located 8 mm from Y1.
The charge-generating layer is measured for the difference in film thickness between the positions Z1 and Z2 (difference in film thickness between the two end portions) and for the difference between the film thickness at the central portion and the average film thickness at the positions Z1 and Z2. The results are shown in Table 2.
Further, measurement results of the spectroscopic absorption ratio obtained for measurement of film thickness are shown in Table 2. The difference in spectroscopic absorption ratio between the end positions Z1 and Z2, and the spectroscopic absorption ratio of the end to the central portion are shown in Table 2.
(Sensitivity)
As sensitivity, VL of a region from the end position Z1 to the end position Z2 is measured.
When the entire area of this region is charged at −700V and irradiated with 3.7 mJ/m2, the average potential in the circumferential direction at intervals of every 90° is measured at measurement points at 5-mm intervals in the axial direction. The result of sensitivity distribution in the axial direction is shown in
ΔVL1 between the end positions Z1 and Z2 (difference in sensitivity between both end portions) is measured. The results are shown in Table 2.
(Image Concentration Unevenness)
A photoreceptor in DOCUPRINT C1616 manufactured by Fuji Xerox is replaced by each of photoreceptor-1 to photoreceptor-6, and in an atmosphere of 20° C. and 50% RH, A4 paper is set such that long side of the paper passes through Y1 in
The results are shown in Table 2.
(Effective Area)
Assuming that an area having an image density unevenness of 0.25 D or less is regarded as an effective region, the ratio of a length of an effective region to the length of the axial direction of the cylindrical support is calculated. In this case a length of an effective region is determined by subtracting, from a length of the base material, an area not satisfying the above standard as length not utilized in image formation.
When
Another exemplary embodiment of the present invention is shown below.
In a method of producing the electrophotographic photoreceptor comprising:
preparing a charge-generating layer coating solution which contains a charge-generating material;
forming, on or above the cylindrical support, a charge-generating layer in which the thickness thereof increases from a central portion in the axial direction of the cylindrical support towards both end portions thereof and the difference in thickness between the two end portions is 2.5% or less with regard to an average thickness of the charge-generating layer, by controlling at least one of (1) a discharge amount of the charge-generating layer coating solution in an axial direction of the cylindrical support from a droplet discharge head or (2) the scanning speed of the droplet discharge head in the axial direction; and
forming a charge-transporting layer on the charge-generating layer,
The foregoing description of the exemplary embodiments of the present invention has been provided for the purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise forms disclosed. Obviously, many modifications and variations will be apparent to practitioners skilled in the art. The exemplary embodiments were chosen and described in order to best explain the principles of the invention and its practical applications, thereby enabling others skilled in the art to understand the invention for various embodiments and with the various modifications as are suited to the particular use contemplated. It is intended that the scope of the invention be defined by the following claims and their equivalents.
All publications, patent applications, and technical standards mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication, patent application, or technical standard was specifically and individually indicated to be incorporated by reference.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2006-254760 | Sep 2006 | JP | national |
| Number | Name | Date | Kind |
|---|---|---|---|
| 7316876 | Kobayashi | Jan 2008 | B2 |
| 20050271959 | Kobayashi | Dec 2005 | A1 |
| 20080014530 | Kawamura | Jan 2008 | A1 |
| Number | Date | Country |
|---|---|---|
| A 47-30330 | Nov 1972 | JP |
| A 61-151665 | Jul 1986 | JP |
| A 4-130433 | May 1992 | JP |
| A 4-189873 | Jul 1992 | JP |
| A-05-019500 | Jan 1993 | JP |
| A 5-43813 | Feb 1993 | JP |
| A 5-98181 | Apr 1993 | JP |
| A 5-140472 | Jun 1993 | JP |
| A 5-140473 | Jun 1993 | JP |
| A 5-263007 | Oct 1993 | JP |
| A 5-279591 | Oct 1993 | JP |
| A-08-044088 | Feb 1996 | JP |
| A-08-095430 | Apr 1996 | JP |
| A 8-176293 | Jul 1996 | JP |
| A 8-208820 | Aug 1996 | JP |
| A-09-265195 | Oct 1997 | JP |
| A 2002-174910 | Jun 2002 | JP |
| A-2004-029134 | Jan 2004 | JP |
| Number | Date | Country | |
|---|---|---|---|
| 20080070134 A1 | Mar 2008 | US |
