JP2012078642A - Image forming device and process cartridge for image forming device - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an image forming device for achieving a high image quality by narrowing a development gap by stabilizing the behavior of a cleaning blade or a lubricant film forming blade and preventing a solid aggregated lubrication material from passing through a blade to mix into a developing device.SOLUTION: An image forming device comprises an image carrier and lubricant applying means for applying a lubricating material on the image carrier surface and has a cleaning blade and/or a lubricant film forming blade as cleaning means or the lubricant applying means. The image carrier has waviness in which the arithmetic average waviness Wa obtained from the waviness curve where a coarse component is eliminated by a λc profile curve filter of 0.25 mm and a wavelength component longer than waviness is eliminated by a λf profile curve filter of 2.5 mm is 0.050 μm or more and 0.30 μm or less and the average length WSm of a profile curve element is 0.50 mm or more and 1.50 mm or less on the surface. The developing means has a developing gap of 0.1 mm or more and 0.5 mm or less.

Description

  The present invention relates to an electrophotographic copying machine, a laser printer, an image forming apparatus such as a facsimile, and a process cartridge.

  2. Description of the Related Art In recent years, image forming apparatuses such as electrophotographic laser printers and digital copying machines have been widely spread due to their improved image quality and stability. The image carrier used in these image forming apparatuses has a function of forming an electrostatic latent image on the surface by charging and exposure, and developing a visible image by developing the electrostatic latent image. The image carrier is also included in the image carrier (hereinafter, the image carrier may be referred to as an electrophotographic photoreceptor or a photoreceptor).

  As electrophotographic photoreceptors, organic photoreceptors mainly using organic materials are widely used because of cost, productivity, freedom of material selection, influence on the global environment, and the like. Recently, the diameter of the photoconductor has been reduced due to the downsizing of the image forming apparatus, and the high speed of the machine and the maintenance-free movement have been added to increase the durability of the photoconductor. In addition, due to the demand for higher image quality, cleaning properties are also demanded as the toner particles become smaller. Therefore, in order to increase the durability of the organic photoreceptor, the surface of the image carrier is roughened in order to form a crosslinked cured film on the surface layer in order to reduce the amount of wear described above, and to provide better cleaning properties. An image forming apparatus having a step of applying a lubricant to a surface of the image bearing member or a surface of the image bearing member is conceivable and already known.

  In the electrophotographic system, there is a developing device for supplying toner to an electrostatic latent image formed on an image carrier. It is already known that a developing device having a higher developing ability can supply toner more stably, can prevent density unevenness, and can reduce density unevenness by narrowing the development gap. However, when the developing gap is narrowed in the conventional image forming apparatuses, there is a problem that the lubricating material applied to the surface of the image carrier is mixed into the developing apparatus as a solid lump and causes an abnormal image.

  Patent Document 1 discloses an image forming apparatus, a process cartridge, and an image forming method that can both suppress the wear of an image carrier and maintain a cleaning property even under AC superimposed charging, and that can output a good image over a long period of time. For the purpose of providing, using an electrostatic latent image carrier and a discharge generated by applying a voltage containing an AC component to a charging member provided in contact with or in proximity to the electrostatic latent image carrier. Charging means for charging the electrostatic latent image carrier, developing means for developing the electrostatic latent image formed on the electrostatic latent image carrier with toner, cleaning means for cleaning using a blade, In an image forming apparatus having at least a lubricant application means for rubbing and scraping a solid lubricant with a brush-like roller and applying the solid lubricant to the surface of the electrostatic latent image carrier, the electrostatic latent image carrier is formed on the surface. And a crosslinked layer obtained by curing a polymerizable monomer having no charge transporting structure and a polymerizable compound having a charge transporting structure, and the ten-point average roughness Rz of the crosslinked layer surface is 0.4 to 1.0. An image forming apparatus having a surface layer in the range of (μm) is disclosed.

The knowledge that this image forming apparatus needs to optimize the surface roughness of the photoreceptor in order to stably supply the lubricant to the surface of the photoreceptor in the apparatus provided with the lubricant application means for applying the lubricant. Based on the above, the surface of the image bearing member is roughened so that Rz is 0.4 to 1.0 μm, thereby achieving both suppression of photoconductor wear and maintenance of cleaning properties.
However, in this image forming device, when the cleaning blade is worn out, the lubricating substance passes through in a solid state and enters the developing device. Not.

Patent Document 2 discloses that the photosensitive layer is rubbed and cleaned with a cleaning blade via a sliding material for the purpose of providing a “method for satisfactorily cleaning an electrophotographic photosensitive member having a smoother photosensitive surface”. In the electrophotographic photosensitive member cleaning method, the average surface roughness Ra of the photosensitive layer is in the range of the following formula (1), the unevenness average interval Sm is in the range of the following formula (2), and Ra and Sm Satisfies the relationship of the following formula (3).
0.01 μm ≦ Ra ≦ 1.1 μm (1), 100 μm ≦ Sm ≦ 3000 μm (2)
1.5 × 10 ⁻³ Sm + 0.45 ≧ Ra ≧ 4 × 10 ⁻⁴ Sm−0.6 (3) ”is disclosed.

  In this invention, the cleaning of the organic photoreceptor is not limited to the average surface roughness of the image bearing member, but also the defective cleaning due to the developer passing through the blade by setting the irregularity period (average irregularity interval) to a specific range. Based on the knowledge that the problem can be solved, the average surface roughness Ra of the surface of the image bearing member is set to 0.01 μm ≦ Ra ≦ 1.1 μm, and the unevenness average interval Sm is set to a range of 100 μm ≦ Sm ≦ 3000 μm. However, even with this method, the problem that “the lubricating substance slips through the cleaning blade in a solid state” cannot be solved.

  The present invention stabilizes the behavior of a cleaning blade or a lubricant film forming blade (hereinafter may be collectively referred to as a blade), so that a solid lubricant material slips through the blade and enters the developing device. It is an object of the present invention to provide an image forming apparatus that can suppress the image quality and thereby can narrow the development gap and realize high image quality.

(1) An image carrier, an electrostatic latent image forming unit that forms an electrostatic latent image on the image carrier, and a developing unit that develops the electrostatic latent image with toner to form a visible image. Transfer means for transferring the visible image to a recording medium, cleaning means for cleaning residual deposits on the surface of the image carrier after transfer, and lubricant application means for applying a lubricating substance to the surface of the image carrier. In the image forming apparatus having at least, the image carrier has a wavy curve on the surface of which a roughness component is blocked by a λc contour curve filter 0.25 mm and a wavelength component longer than the waviness is blocked by a λf contour curve filter 2.5 mm. Image bearing member having a swell in which the arithmetic average swell Wa (μm) is 0.050 μm or more and 0.30 μm or less and the average length WSm (mm) of the contour curve elements is 0.50 mm or more and 1.50 mm or less. And The developing means has a developing means with a development gap of 0.1 mm or more and 0.5 mm or less, and the cleaning means or the lubricant application means has a cleaning blade and / or a lubricant film forming blade. Image forming apparatus.
(2) The image forming apparatus according to (1), wherein the surface layer of the image carrier contains a filler.
(3) The image forming apparatus according to (1) or (2), wherein the surface layer of the image carrier is a cross-linked surface layer.
(4) The image forming apparatus according to any one of claims 1 to 3, wherein the surface layer of the image carrier is a cross-linked surface layer and contains a filler.
(5) The cross-linked surface layer contains a cross-linked product composed of a polymerizable compound having a charge transporting structure and a tri- or higher functional polymerizable monomer not having a charge transporting structure. Item 5. The image forming apparatus according to Item 3 or 4.
(6) The image forming apparatus according to any one of (1) to (5), wherein the lubricating substance contains a fatty acid metal salt.
(7) The image bearing member and at least one selected from the group consisting of an electrostatic latent image forming unit, an exposure unit, a developing unit, a transfer unit, and a cleaning unit, according to any one of claims 1 to 6. A process cartridge which is detachable from an image forming apparatus, wherein the image carrier has a surface on which the roughness component is cut off by a λc contour curve filter of 0.25 mm, and the wavelength longer than the undulation by a λf contour curve filter of 2.5 mm. Arithmetic mean waviness Wa (μm) obtained from the waviness curve in which the components are blocked is 0.050 μm or more and 0.30 μm or less, and the average length WSm (mm) of the contour curve element is 0.50 mm or more and 1.50 mm or less. A process cartridge for an image forming apparatus, which is an image carrier having a certain undulation.

  According to the present invention, even when a cleaning blade or a lubricant film forming blade that has been used and deteriorated over a long period of time is used, the behavior of the blade is stabilized and it is possible to prevent the solid lubricant from slipping through. Thus, the developing gap can be narrowed, the developing ability can be improved, and high image quality can be realized.

It is a figure which shows the example of the image forming apparatus of this invention. It is a figure which shows the example of a layer structure of an image carrier. It is a figure explaining the other example of the layer structure of an image carrier. It is a figure which shows the outline | summary of a spray coating process. It is a figure which shows the structure of a developing device. It is a figure which shows the structure of the film formation member of a lubricous substance. It is a figure which shows the example of the full-color image forming apparatus by a tandem system. It is a figure which shows the other example of the full color image forming apparatus by a tandem system. It is a figure which shows the example of a process cartridge. It is a figure which shows the example of formation of the image for evaluation for evaluating a cleaning defect.

The form for implementing this invention is demonstrated below.
The present invention has the following characteristics in an image forming apparatus in which operations such as lubricant application, electrostatic latent image formation, toner development, toner image transfer, and image carrier surface cleaning after transfer are repeatedly performed.
In other words, the image forming apparatus of the present invention has a “lubricant applying means for applying a lubricating material to the surface of the image carrier, and the roughness component is blocked on the surface of the image carrier by a λc contour curve filter 0.25 mm. , The arithmetic average waviness Wa (μm) obtained from the waviness curve obtained by blocking the wavelength component longer than the waviness by the λf contour curve filter 2.5 mm is 0.050 μm or more and 0.30 μm or less, and the average length WSm ( mm) is a carrier having a swell of 0.50 mm or more and 1.50 mm or less, and has a developing means having a development gap of 0.1 mm or more and 0.5 mm or less, and an image carrier after transferring a toner image. It has a cleaning blade for cleaning the surface and / or a blade for forming a lubricant film ”.
The configuration of the image forming apparatus according to the present invention will be described in detail below.

<Swelling of the surface of the image carrier>
In the image forming apparatus, by narrowing the developing gap, the electric field of the developing bias can be increased, the image density can be increased, and the image density unevenness can be reduced. For example, if the development gap can be narrowed to 0.1 mm or more and 0.5 mm or less, the effect of increasing the image density becomes remarkable.
By applying a lubricating substance to the surface of the image carrier, the friction coefficient of the surface of the image carrier can always be kept small, the lubricity is improved, and the blade behavior can be stabilized. Good cleaning properties can be obtained. However, when the blade deteriorates due to long-term use and wear of the edge portion progresses, a solid lubricating material may slip through the blade. When the development gap is narrowed as described above, a slipping solid lump-like lubricating substance may enter the developing device and cause development failure.

The inventors of the present invention have an arithmetic mean waviness Wa of 0.050 μm or more and 0.30 μm or less and an average length WSm of the contour curve element of 0.50 mm or more and 1.50 mm or less. When the blade vibrates in accordance with the size of the undulation of the image carrier, the solid lump-like lubricant can be applied to the surface of the image carrier while crushing. It has been found that the development gap can be narrowed without problems, and high image quality can be achieved.
Further, the cleaning blade has an action of crushing the solid lump-like lubricating substance, and has an effect of preventing the accumulation of the solid lump-like lubricating substance.
It is preferable to use a cleaning blade and a lubricant film forming blade in combination.

  The present invention is based on the above-described knowledge. Therefore, the image forming apparatus of the present invention blocks the roughness component on the surface of the image carrier with a λc contour curve filter 0.25 mm, and the λf contour curve filter 2.5 mm. The arithmetic average waviness Wa (μm) obtained from the waviness curve in which the wavelength component longer than the waviness is cut off is 0.050 μm or more and 0.30 μm or less, and the average length WSm (mm) of the contour curve element is 0.50 mm or more and 1 It is characterized by using an electrophotographic photosensitive member having a swell of 50 mm or less.

When the arithmetic average waviness Wa is larger than 0.30 μm, the solid lump-like lubricating material may slip through. When Wa is less than 0.050 μm, the undulation of the surface of the image carrier is small, so that the vibration amplitude of the blade is small, and the solid lump-like lubricating substance cannot be broken, and fine lumps may slip through.
When the average length WSm of the contour curve element is larger than 1.50 mm, the blade frequency becomes small, and the cleaning effect is reduced. When WSm (mm) is smaller than 0.50 mm, the vibration amplitude of the blade is small, and the solid lump-like lubricating material may not be crushed.

  The waviness of the surface of the image carrier is preferably such that the arithmetic average waviness Wa is 0.10 μm or more and 0.27 μm or less, and the average length WSm of the contour curve elements is 0.60 mm or more and 1.30 mm or less, and Wa is 0. More preferably, it is not less than 13 μm and not more than 0.25 μm, and WSm is not less than 0.70 mm and not more than 1.20 mm.

  The arithmetic average waviness Wa and the average length WSm of contour curve elements in the present invention are parameters obtained from a waviness curve obtained by removing a short wavelength roughness component of 0.25 mm or less and a wavelength component of 2.5 mm or more. The arithmetic average waviness Wa and the average length WSm of the contour curve element of the present invention are based on JIS B 0601: 2001 standard, and the λc contour curve filter 0.25 mm blocks the roughness component, and the λf contour curve. Measurement is performed by obtaining a waviness curve in which a wavelength component longer than the waviness is cut off with a filter of 2.5 mm. The reason why the present invention calculates the parameters from the waviness curve obtained by removing the short wavelength roughness component of 0.25 mm or less and the wavelength component of 2.5 mm or more is that, in the present invention, the average length WSm of the contour curve element is The wave of 0.50 mm or more and 1.50 mm or less is found to be important, and if the λc contour curve filter and λf contour curve filter do not block, the short wavelength component or the long wavelength component is detected, and the present invention is important. This is because the swell component is sometimes not measured.

In the present invention, the measurement is performed using a surface roughness meter Surfcom 1400D manufactured by Tokyo Seimitsu, but any measuring device may be used as long as it conforms to the JIS standard and can perform the same measurement.
There are no restrictions on the measurement position or the number of measurements, but it is preferable to measure multiple points in order to reduce measurement errors. For example, in the case of a cylindrical image carrier, measurement is performed at a total of 12 points, that is, 3 points at the upper end, center, and lower end in the longitudinal direction and 4 points every 90 ° in the circumferential direction. A small value can be obtained.
In the present invention, the measurement was performed at a reference length of 2.5 mm, a measurement length of 12.5 mm, and a measurement speed of 0.60 mm / s.

  Conventionally, control of the shape of the surface of the image bearing member has been studied. For example, a method of adding a filler and adjusting the surface roughness according to the particle size or added amount of the filler (Japanese Patent Laid-Open No. 52-026226, JP No. 4056097), a method of polishing after forming a coating film on the surface layer (Japanese Patent Laid-Open No. 02-139666, Japanese Patent Laid-Open No. 2006-301092), and a method of mechanically forming a surface roughness by sandblasting (Japanese Patent Laid-Open No. 02). -150850 and Japanese Patent No. 3938210). However, although fine irregularities are formed by surface control with a filler, it is difficult to form large waviness as in the present invention, and even in the method of mechanically forming surface roughness, streaks are formed. It was difficult to form a swell due to the surface shape or dimple shape. In addition, as a general method for forming the surface layer, there are a dip coating method, a ring coating method, a roll coating method, a spray coating method, and the like. Thus, it was difficult to form a surface shape with large undulations.

  On the other hand, as a result of the inventor's investigation, it was found that a surface shape having a large swell can be formed by appropriately controlling the prescription of the coating liquid and the coating conditions using the spray coating method. It was. The waviness shape control can be performed by controlling the atomizing air pressure during spray coating and the viscosity of the coating liquid.

  An example of a method for controlling swell is shown below, but the swell control method of the present invention is not limited to this. When the surface layer is formed by spray coating method and the undulation is controlled, any spray gun can be used at the time of spray coating, but the discharge amount of the coating liquid, the atomizing air flow rate, the atomizing air pressure, etc. can be controlled. Those are preferred. Examples of the spray gun include air spray, airless spray, electrostatic spray and the like. The spray may be vertical or horizontal. In the examples of the present invention, coating was performed using an air spray A100 manufactured by Meiji Machinery Co., Ltd.

  FIG. 4 shows an outline of spray coating. Reference numeral (A) indicates a spray gun, and reference numeral (B) indicates a substrate to be coated. In FIG. 4, the substrate (B) is a cylindrical support member, and shows an image carrier production stage product before the surface layer is applied. The substrate (B) is rotated in the direction of the arrow by the driving means, and the spray gun (A) is applied to the substrate while atomizing the surface layer coating liquid. The spray gun (A) moves slowly from the left end of the substrate (B) in the direction of the arrow, and coats the entire surface of the substrate (B) with the surface layer coating solution. The number of coating times of the surface layer coating solution is arbitrary.

In order to form the wave | undulation of this invention, it can carry out by controlling the atomization air pressure at the time of spray coating, and the liquid viscosity of a coating liquid. To obtain a swell defined in the present invention, depending on the spray gun, atomization air pressure during spray coating is generally preferable to be 0.6 kgf / cm ² or more 1.2 kgf / cm ² or less. When the atomizing air pressure is made smaller than 0.6 kgf / cm ² , the shape rougher than the undulation of the present invention, that is, Wa is larger than 0.30 μm and WSm may be smaller than 0.5 mm. Further, when the atomizing air pressure is made larger than 1.2 kgf / cm ² , the shape smoother than the swell of the present invention, that is, Wa may be smaller than 0.05 μm and WSm may be larger than 1.5 mm.

In order to obtain the swell defined in the present invention, the viscosity of the coating solution is preferably 0.5 mPa · s to 5 mPa · s, and more preferably 0.5 mPs to 2 mPa · s. When the viscosity is higher than 5 mPa · s, it is difficult to control the surface shape. The method for adjusting the viscosity of the coating solution is preferably adjusted by the solvent used in the coating solution. Any method may be used for measuring the viscosity. In Examples of the present invention, a TV-30 viscometer (manufactured by Toki Sangyo Co., Ltd.) was used, and measurement was performed at a rotation speed of 20 rpm and a liquid temperature of 22 ° C.
The film thickness of the coating film is preferably controlled by the discharge amount, the spray moving speed, and the number of coatings.
Moreover, it is also possible to form a wave | undulation by spraying a solvent and air with the coating liquid in the wet state immediately after a coating film. When the solvent is sprayed, the type of the solvent is arbitrary, but a solvent having a low boiling point is preferable so as not to remain on the coating film surface after spraying.

  After coating the surface layer, it is necessary to dry the coating film. In the case of a crosslinkable coating solution, a step of curing the coating film is required after spray coating. The time from application of the surface layer to drying or curing (hereinafter referred to as finger touch drying time) is preferably within 10 minutes. When the touch drying time is long, the coating film is leveled, the waviness shape becomes small and may disappear.

<About development means>
In the image forming apparatus of the present invention, there is provided developing means for developing the electrostatic latent image formed by the exposure means with toner and forming a toner image on the image carrier. A negative image (reversal development) can be obtained by developing with a toner having the same polarity as the charged polarity of the image carrier, and a positive image can be obtained by developing with a toner of a different polarity. Development includes a one-component development system that uses only toner and a two-component development system that uses a mixture of toner and carrier, and both can be used satisfactorily in the present invention. Further, when developing a full-color image by superimposing a plurality of color toner images on the image carrier, using the method of developing in contact with the image carrier will disturb the previously developed toner image. There is a fear. For this purpose, for example, a jumping development system that can be developed without contact with the image carrier is preferably used.

  FIG. 5 is a schematic diagram for explaining the developing device. This is one representative example, and the present invention is not limited to this. The surface of the image carrier 1 on which the electrostatic latent image is formed reaches the developing device 4 and is developed to form a toner image. The developing device includes a developer agitation tank 56 and a toner storage tank 57, and the developer agitation tank 56 contains a two-component developer including a toner and a carrier. The toner is originally stored in the toner storage tank 57 or is supplied from a toner cartridge (not shown) to the toner storage tank 57 via a toner supply pipe, and is further supplied from the toner storage tank 57 via the toner supply roller 55 to the developer agitation tank. 56. The developer agitation tank 56 is provided with an agitation screw 54 for agitating the developer. The agitation screw mixes and agitates the developer composed of toner and carrier in the developer agitation tank 56 and develops the developer carrier (developing roller). ) Refill on 52. The developer replenished on the developing roller 52 is regulated to an appropriate amount by the doctor blade 53, and then conveyed to the developing position facing the image bearing member, and the image bearing member is formed by the electric field formed at the developing position. A toner image is formed on the electrostatic latent image formed above.

  The present invention is characterized in that a distance X (hereinafter referred to as “development gap”) between the image carrier and the developing roller is 0.1 mm to 0.5 mm. Since the developing bias electric field can be increased as the developing gap X is smaller, the developing ability is improved and a high-quality image can be obtained. Further, density unevenness due to development can be reduced by setting the development gap to 0.5 mm or less. When the development gap is larger than 0.5 mm, the electric field of the development bias is reduced, the image density is lowered, and the density unevenness becomes remarkable. Further, if the development gap is less than 0.1 mm, it is difficult to control practically. By reducing the developing gap, there is a problem that a lump of a lubricating substance that has not been satisfactorily applied to the image carrier easily enters the inside of the developing device, the carrier and toner are fixed, and the developing ability is lowered. However, by providing the surface of the image carrier of the present invention with undulations, it is possible to prevent the lubricating material on the solid mass from passing through the cleaning blade and entering the developing device, and the development gap can be narrowed. It became. The developing gap of the present invention is from 0.1 mm to 0.5 mm, more preferably from 0.2 mm to 0.4 mm. The development gap can be adjusted by inserting a spacer outside the image area of the photosensitive member or the developing roller, or by covering the shaft end portion of the photosensitive member or the developing roller with a color.

<About cleaning means>
The cleaning process is a process in which the toner developed on the image carrier by the developing unit is transferred to the transfer medium by the transfer unit, and the toner remaining on the image carrier is removed. Any method may be used as long as these residual toners can be removed from the image carrier. As specific means, a fur brush, a blade, a magnetic brush, an electrostatic brush, a magnetic roller, or the like can be used effectively, or a combination thereof can be used. Among these, in the present invention, at least a cleaning blade is used as a cleaning means in order to improve cleaning properties and prevent filming. However, when a brush is used in combination with the cleaning means, the cleaning means and the lubricating substance supply means can be integrated with each other by bringing the lubricating substance into contact with the brush. As a material of the cleaning blade, for example, urethane rubber can be used.

  The cleaning process is contaminated by the adhering of many foreign substances such as developer components, paper dust, and discharge products in addition to the residual toner on the image carrier, which greatly affects the image quality. It also has a role to remove. In that respect, the cleaning blade is considered excellent. However, if the foreign matter adheres to the surface of the image carrier as it is repeatedly used, the behavior of the cleaning blade becomes unstable, causing a defective cleaning and causing an abnormal image. In the present invention, the image carrier protecting agent is applied to the surface of the image carrier, and the uneven shape on the surface of the image carrier is stably maintained for a long time. The behavior is stabilized, and as a result, it is possible to obtain an effect that the foreign matter is less likely to adhere or is easily removed. Further, friction with the cleaning blade is reduced, and it becomes possible to prevent cleaning failure and filming. The present invention has the effect that the above effect can be stably exhibited over a long period of time by controlling the uneven shape on the surface of the image carrier, and the merit can be maximized by using a cleaning blade as a cleaning means. The In the present invention, it is more preferable that the cleaning blade is in contact with the rotation direction of the image carrier in the counter direction. Thereby, it is possible to prevent the toner from slipping through the blade, which is effective in enhancing the effects of the present invention.

<About lubricant application means>
In the present invention, as described above, the lubricant application means for supplying a specific lubricating substance to the surface of the image carrier is provided. In the present invention, by applying a specific lubricating material to the surface of the image carrier, the transfer efficiency of toner is increased and the cleaning property is improved. As a result, it is possible to prevent image blurring, poor cleaning, and filming. Is possible. In addition, since a lubricating substance is applied to the surface of the image carrier, it also has the effect of preventing deterioration of the surface of the image carrier due to charging, and as a result, the wear resistance and scratch resistance of the image carrier are significantly improved. And the uneven | corrugated shape of a surface is maintained stably, and it becomes possible to maintain the said effect over a long period of time.

  Lubricating substance is applied by solidifying the lubricating substance, scraping it with a brush and applying it to the image carrier, applying the lubricant directly in contact with the image carrier, and lubricating the developer. There are many methods such as a method in which the active substance is mixed in the form of a powder and supplied and applied to the surface of the image carrier in the development step. In the present invention, any method can be used as long as a lubricating substance is applied to the surface of the image carrier, but a method of scraping and applying the lubricating substance with a brush is particularly preferred. For example, the lubricant application device 30 of FIG. 1 has a lubricating material 32, a fur brush 31 as an application member, and a pressure spring 33 for pressing the lubricating material 32 against the fur brush 31. The lubricating material 32 is formed into a bar shape and solidified. The lubricating material 32 is pressed against the pressure spring 33 with a predetermined pressure, and the fur brush 31 is rotated to scrape off the lubricating material, whereby the image carrier 1. It is structured to be applied to the surface of The pressurizing spring 33 is effective in always supplying the same amount of the lubricating substance by the fur brush 31 to the surface of the image carrier even if the lubricating substance decreases with time.

  Further, in order to apply an appropriate amount and a uniform amount of a lubricating substance on the surface of the image carrier, there is a method in which a film forming blade is brought into contact and the applied lubricating substance is spread on the surface of the image carrier to form a film. It is effective and preferably used. FIG. 6 shows an example of a film forming member made of a lubricating substance. The lubricating substance supply device 20 disposed opposite to the image carrier 1 includes a lubricating substance (hereinafter also simply referred to as “protective agent”) 21 formed in a columnar shape or a bar shape, and a lubricating substance supply member. 22, a pressing force applying mechanism 23, a film forming mechanism 24 of a lubricating material, and the like. The film forming mechanism 24 of the lubricating substance urges the blade 24a in contact with the image carrier 1, the blade support 24b that supports the blade 24a, and the blade 24a together with the blade support 24b toward the image carrier 1 side. It has a biasing means 24c. Here, a coil spring is illustrated as an urging means for the pressing force applying mechanism 23 and the film forming mechanism 24 of the lubricating material. However, the present invention is not limited to this, and for example, a member having elastic elasticity, a leaf spring, and the like. The elastic member may be used. The protective agent 21 is brought into contact with the lubricating substance supply member 22 made of, for example, a rotating brush by the pressing force from the pressing force applying mechanism 23. The lubricating substance supply member 22 rotates and rubs with the image carrier 1 with a linear velocity difference, and supplies the lubricating substance held on the surface of the protective agent supply member 22 to the surface of the image carrier at this time. . The lubricating material supplied to the surface of the image carrier is thinned (filmed) by the film forming mechanism 24 of the lubricating material.

  Although the blade for forming a film of the lubricating material can be used in combination with the cleaning blade, it is more preferable to provide it separately from the cleaning blade. In this case, it is more preferable that the film forming blade 24a is in contact with the rotation direction of the image carrier so as to be in the trailing direction. As a result, the spreadability of the lubricating substance is enhanced, and the effect of improving the cleaning property is sufficiently exhibited even with a small amount of the lubricating substance. The film forming blade also vibrates due to the undulations on the surface of the image carrier, and has an effect of applying a solid lump-like lubricating material while crushing. Therefore, when used in combination with the cleaning blade, slipping of the lubricating substance can be more effectively suppressed. It is preferable that these lubricant-forming film-forming members are disposed in a subsequent step of the lubricant-substance supplying means. As a material for the film forming blade, for example, urethane rubber can be used.

The deteriorated lubricating substance is removed by the cleaning device 8 together with other components such as toner remaining on the image carrier. Although the cleaning device 8 and the lubricating substance supply device 20 may be combined, the function of removing the image carrier surface residue and the function of forming a film of the lubricating substance are determined by the frictional state of an appropriate member. In this embodiment, the functions are separated, and cleaning is performed downstream of the transfer device in the rotation direction of the image carrier 1 and upstream of the lubricating substance supply device 20 as shown in FIG. A device 8 is provided.
The cleaning device 8 includes a cleaning blade 8 as a cleaning member, a cleaning blade pressing mechanism 8b, and the like. Here, a coil spring is illustrated as the cleaning blade pressing mechanism 8b, but the present invention is not limited to this, and for example, a member having rubber elasticity, a leaf spring, and other elastic members may be used.

  As the lubricating substance used in the present invention, any substance can be used as long as it adheres uniformly to the surface of the image carrier and as a result can impart lubricity to the surface of the image carrier. For example, lead oleate, zinc oleate, copper oleate, zinc stearate, cobalt stearate, iron stearate, copper stearate, calcium stearate, aluminum stearate, zinc palmitate, copper palmitate, zinc linolenate, etc. Fatty acid metal salts, polytetrafluoroethylene, polychlorotrifluoroethylene, polyvinylidene fluoride, polytrifluorochloroethylene, dichlorodifluoroethylene, tetrafluoroethylene-ethylene copolymer, tetrafluoroethylene-oxafluoropropylene copolymer, etc. And fluororesin. Waxes can also be used, and ester or olefin types are effective. The ester wax has an ester bond, and examples thereof include natural waxes such as carnauba wax, candelilla wax and rice wax, and montan wax. Examples of the olefin wax include synthetic waxes such as polyethylene wax and polypropylene wax. Among these, a high effect is obtained with a small amount of coating, the effect of protecting the surface of the image carrier is high against charging, and examples of the most usable in the present invention include fatty acid metal salts. By containing the fatty acid metal salt, the lubricating substance is smoothly applied to the surface of the image bearing member, and the effect that the behavior of the cleaning blade is stabilized can be obtained. As the fatty acid metal salt, a metal stearate is preferable, and zinc stearate is particularly preferable.

<About image forming apparatus>
FIG. 1 is a schematic view for explaining an image forming apparatus of the present invention. This is one representative example, and the present invention is not limited to this example. For example, all modifications described later are included in the present invention. 1 shown in FIG. 1 is an image carrier, which shows a drum shape, but is not limited thereto, and may be in the form of a sheet or an endless belt, for example. Reference numeral 2 denotes a charging means, which is shown by a roller charging system, but is not limited to this, and any system such as a corona charging system may be used. A latent image forming unit 3 is an exposure unit for forming an electrostatic latent image on the image carrier. Reference numeral 4 denotes a developing device, 5 denotes a transfer device, and 6 denotes a fixing device, and any conventionally known system can be used effectively. Reference numeral 8 denotes a cleaning device, which indicates a cleaning blade. 9 is a static eliminating device, 10 is a transfer material conveyance path, and 30 is a lubricant application device. The image forming apparatus of the present invention has at least a specific image carrier, a charging unit, a developing unit, and a lubricant coating unit, and further, as an electrostatic latent image forming unit, an exposure unit, a transfer unit, a cleaning unit, a fixing unit, A neutralizing means or the like can be provided as necessary. Any other means can be added as appropriate.

<Charging means>
As the charging means 2 in the present invention, any conventionally known charging means can be used. For example, a corona discharge method that applies high voltage to wires such as corotron and scorotron, a solid discharge method that applies high-frequency and high-voltage to a planar electrode that sandwiches an insulating plate instead of a wire, and a high voltage to a roller-shaped member A contact-type roller charging method in which charging is performed while being in contact with the image carrier, a proximity-arranged roller charging method in which charging is performed through a gap of 100 μm or less in the image forming region having a roller shape, other brushes, There is a contact charging method in which charging is performed in contact with the image carrier using a film, a blade, or the like, and any conventionally known charging means can be used.

<About exposure means>
Examples of the latent image forming device 3 include exposure means for forming an electrostatic latent image on the image carrier. As the exposure means, any means can be used as long as the irradiated light is absorbed by the charge generating material of the image carrier. The charged image carrier is exposed to light, and the light is absorbed by the charge generating material to generate charge pairs. One charge moves to the surface and cancels the surface charge, thereby electrostatic latent on the surface of the image carrier. An image is formed. As a light source used as an exposure means, a light emitting diode (LED), a semiconductor laser (LD), an electroluminescence (EL), a tungsten lamp, a halogen lamp, a mercury lamp, a fluorescent lamp, a sodium lamp, etc. are used if the above conditions are satisfied. be able to. Among these, light emitting diodes and semiconductor lasers are effective from the viewpoint of speeding up and downsizing the apparatus, and are most suitable for further enhancing the effects of the present invention. These light sources are combined with various filters such as sharp cut filters, band pass filters, near infrared cut filters, dichroic filters, interference filters, and color temperature conversion filters in order to irradiate light in a desired wavelength range. It can also be used.

  Further, as the exposure means, the multi-beam exposure means is also effectively used in the present invention. In order to cope with the high speed of the image forming apparatus, it is necessary to increase the rotation speed of the polygon mirror of the rotating multi-specular body and increase the image scanning frequency in the sub-scanning direction. However, the rotational speed of the polygon mirror is also limited. In this case, a multi-beam scanning exposure method using a multi-beam recording head is used in which a plurality of beam light sources are arranged in the sub-scanning direction and a plurality of beams are scanned by one scan in the main scanning direction. In this method using a multi-beam recording head, for example, the number of rotations of the polygon mirror of the rotating polyhedral body that is necessary when only one beam light source is obtained by using n beam light sources may be 1 / n. Thus, the speed can be increased by n times as compared with the case of the single beam light source. In addition, there is a margin in the scanning speed, and there is a great merit that the scanning density is increased by that amount, and high-speed and high-definition image output becomes possible.

<About transfer means>
The transfer device 5 is a device that transfers the toner image formed on the image carrier onto a transfer material (transfer medium such as paper). As the transfer means, a charger can be used. For example, a transfer charger or a combination of a separation charger is effective. As a transfer method, a method of directly transferring a toner image from an image carrier to a transfer medium such as paper using the above transfer means, and a toner image on the image carrier once transferred to an intermediate transfer member, and then an intermediate transfer member There is an intermediate transfer method for transferring to a transfer medium such as paper, and either method can be used satisfactorily.
Further, there are a constant voltage method and a constant current method at the time of transfer, and either method can be used. However, the constant current method which can keep the transfer charge amount constant and is excellent in stability is more preferable. The higher the transfer current is, the higher the transferability becomes. In particular, when the linear velocity is increased, the transferability is lowered, so that an increase in the transfer current is effective. In addition, when the transfer current is increased, the amount of charge flowing in the image carrier during charge removal is reduced, which is preferable in reducing the influence of electrostatic fatigue. However, if the transfer current is too high and the surface of the image bearing member is positively charged, the potential difference cannot be erased even in the static elimination process, and there is a possibility of causing a decrease in charge when entering the charging process of the next cycle.

<About fixing means>
The fixing device 6 is a device that fixes a toner image transferred to a transfer medium such as paper on the transfer medium by heating and pressing. As a fixing method, any method may be used as long as the toner can be fixed to the transfer medium. Specifically, a method of heating and / or pressing can be mentioned, and a combination of a heating roller and a pressing roller, and a method of combining an endless belt can also be used.

<About static elimination means>
If the electrostatic latent image contrast remains on the image bearing member even if the residual toner is removed in the cleaning process, the neutralization device 9 may be visualized as an afterimage or a ghost image in the next cycle. Therefore, it is a device that removes them. As the charge eliminating means, any means may be used as long as the charge generating substance can absorb the light emitted from it. For example, a light emitting diode (LED), a semiconductor laser (LD), an electroluminescence (EL), a tungsten lamp, a halogen lamp, a xenon lamp, a mercury lamp, a fluorescent lamp, a sodium lamp, and the like. May be used in combination. In addition to the light irradiation method, there is also a method of removing electricity by applying a reverse bias, which is preferable for suppressing electrostatic fatigue.

<About the layer structure of the image carrier>
The layer structure of the image carrier in the present invention is shown.
The image carrier in the present invention has a structure in which a photosensitive layer 202 is provided on a conductive support 201 as shown in FIG. 2, and the photosensitive layer may have a single layer structure or a laminated structure. When the photosensitive layer has a single layer structure, the photosensitive layer 202 is a layer having a charge generation function and a charge transport function at the same time as shown in FIG. When the photosensitive layer has a stacked structure, a stacked structure in which a charge generation layer 203 having a charge generation function and a charge transport layer 204 having a charge transport material function are stacked as shown in FIG. When the photosensitive layer is the surface of the image carrier, the photosensitive layer is a single layer structure, and in the stacked structure, the charge transport layer is a surface layer of the image carrier (hereinafter referred to as “surface layer”). Therefore, the surface of the photosensitive layer or the charge transport layer is provided with undulations.

Also, as shown in FIG. 3, a surface protective layer 205 can be provided on the photosensitive layer, which is effective because the mechanical durability of the image carrier can be improved. 3A shows a case where the surface protective layer 205 is provided on the photosensitive layer 202 having a single layer structure, and FIG. 3-B shows a case where the surface protective layer 205 is provided on the charge transport layer 204 having a laminated structure. When the surface protective layer is provided, the surface protective layer serves as the surface layer of the image carrier, and thus has a structure in which the surface of the surface protective layer is wavy.
In the present invention, an undercoat layer may be provided between the conductive support and the photosensitive layer, and it is preferable to provide an undercoat layer in order to improve chargeability and suppress background stains. The structure of the undercoat layer may be a single layer or a plurality of layers. Note that these layer configurations are representative, and the present invention is not limited to these layer configurations.

<About photosensitive layer>
As described above, the photosensitive layer in the invention may have a single layer structure or a laminated structure.
In the case of a laminated structure, the photosensitive layer is composed of a charge generation layer having a charge generation function and a charge transport layer having a charge transport function. In the case of a single layer structure, the photosensitive layer is a layer having a charge generation function and a charge transport function at the same time. Hereinafter, each of the photosensitive layer having a laminated structure and the photosensitive layer having a single layer structure will be described.

<< Photosensitive layer with laminated structure >>
(Charge generation layer)
The charge generation layer is a layer mainly composed of a charge generation material having a charge generation function, and a binder resin can be used in combination as necessary. As the charge generation material, inorganic materials and organic materials can be used.
Inorganic materials include crystalline selenium, amorphous selenium, selenium-tellurium, selenium-tellurium-halogen, selenium-arsenic compounds, and amorphous silicon. In amorphous silicon, dangling bonds that are terminated with hydrogen atoms or halogen atoms, or those that are doped with boron atoms, phosphorus atoms, or the like are preferably used.
A known material can be used as the organic material. For example, phthalocyanine pigments such as metal phthalocyanine and metal-free phthalocyanine, azulenium salt pigments, squaric acid methine pigments, azo pigments having carbazole skeleton, azo pigments having triphenylamine skeleton, azo pigments having diphenylamine skeleton, dibenzothiophene skeleton Azo pigments having a fluorenone skeleton, azo pigments having an oxadiazole skeleton, azo pigments having a bis-stilbene skeleton, azo pigments having a distyryl oxadiazole skeleton, azo pigments having a distyrylcarbazole skeleton, perylene Pigments, anthraquinone or polycyclic quinone pigments, quinoneimine pigments, diphenylmethane and triphenylmethane pigments, benzoquinone and naphthoquinone pigments, cyanine and azomethine pigments, Goido based pigments, and bisbenzimidazole pigments. These charge generation materials can be used alone or as a mixture of two or more.

  As a binder resin used as necessary for the charge generation layer, polyamide, polyurethane, epoxy resin, polyketone, polycarbonate, silicone resin, acrylic resin, polyvinyl butyral, polyvinyl formal, polyvinyl ketone, polystyrene, poly-N-vinylcarbazole, Examples include polyacrylamide. These binder resins can be used alone or as a mixture of two or more. In addition to the binder resin described above as a binder resin for the charge generation layer, a polymer charge transport material having a charge transport function, such as an arylamine skeleton, benzidine skeleton, hydrazone skeleton, carbazole skeleton, stilbene skeleton, pyrazoline skeleton, etc. Polymer materials such as polycarbonate, polyester, polyurethane, polyether, polysiloxane, and acrylic resin, polymer materials having a polysilane skeleton, and the like can be used.

The charge generation layer may contain a low molecular charge transport material. Low molecular charge transport materials that can be used in the charge generation layer include hole transport materials and electron transport materials. A known material can be used for the low molecular charge transport material, and the materials listed in the charge transport layer described later can be used as an example.
Methods for forming the charge generation layer include a vacuum thin film preparation method and a casting method from a solution dispersion system. For the vacuum thin film production method, a vacuum deposition method, a glow discharge decomposition method, an ion plating method, a sputtering method, a reactive sputtering method, a CVD method, or the like is used, and the above-described inorganic materials and organic materials can be satisfactorily formed. . In order to provide a charge generation layer by a casting method from a solution dispersion, the above inorganic or organic charge generation materials are used together with a binder resin, if necessary, tetrahydrofuran, dioxane, dioxolane, toluene, dichloromethane, monochlorobenzene, dichloroethane, cyclohexanone, Formed by dispersing with a ball mill, attritor, sand mill, bead mill, etc. using a solvent such as cyclopentanone, anisole, xylene, methyl ethyl ketone, acetone, ethyl acetate, butyl acetate, etc. it can. Moreover, leveling agents, such as a dimethyl silicone oil and a methylphenyl silicone oil, can be added as needed. The coating can be performed using a dip coating method, spray coating, bead coating, ring coating method or the like.
The thickness of the charge generation layer provided as described above is suitably about 0.01 to 5 μm, preferably 0.05 to 2 μm.

(Charge transport layer)
The charge transport layer is a layer having a charge transport function, and is formed by dissolving or dispersing a charge transport material having a charge transport function and a binder resin in an appropriate solvent, and applying and drying the solution on the charge generation layer. .
As the charge transport material, an electron transport material, a hole transport material, and a polymer charge transport material can be used. Low molecular charge transport materials include hole transport materials and electron transport materials.
Examples of the electron transporting material include chloroanil, bromanyl, tetracyanoethylene, tetracyanoquinodimethane, 2,4,7-trinitro-9-fluorenone, 2,4,5,7-tetranitro-9-fluorenone, 2,4 , 5,7-tetranitroxanthone, 2,4,8-trinitrothioxanthone, 2,6,8-trinitro-4H-indeno [1,2-b] thiophen-4-one, 1,3,7-tri Examples thereof include electron-accepting substances such as nitrodibenzothiophene-5,5-dioxide and diphenoquinone derivatives. These electron transport materials can be used alone or as a mixture of two or more.

  Examples of the hole transporting material include the electron donating materials shown below and are used favorably. As hole transport materials, oxazole derivatives, oxadiazole derivatives, imidazole derivatives, monoarylamine derivatives, diarylamine derivatives, triarylamine derivatives, stilbene derivatives, α-phenylstilbene derivatives, benzidine derivatives, diarylmethane derivatives, triaryls Other known materials such as a methane derivative, a 9-styrylanthracene derivative, a pyrazoline derivative, a divinylbenzene derivative, a hydrazone derivative, an indene derivative, a butadiene derivative, and a pyrene derivative, a bisstylbene derivative, a distyrylbenzene derivative, and an enamine derivative can be given. These hole transport materials can be used alone or as a mixture of two or more.

  As the binder resin, polystyrene, styrene-acrylonitrile copolymer, styrene-butadiene copolymer, styrene-maleic anhydride copolymer, polyester, polyvinyl chloride, vinyl chloride-vinyl acetate copolymer, polyvinyl acetate, Polyvinylidene chloride, polyarylate resin, phenoxy resin, polycarbonate, cellulose acetate resin, ethyl cellulose resin, polyvinyl butyral, polyvinyl formal, polyvinyl toluene, poly-N-vinyl carbazole, acrylic resin, silicone resin, epoxy resin, melamine resin, urethane resin And thermoplastic or thermosetting resins such as phenol resins and alkyd resins.

The amount of the charge transport material is appropriately 20 to 300 parts by weight, preferably 40 to 150 parts by weight, based on 100 parts by weight of the binder resin. However, when a polymer charge transport material is used, it can be used alone or in combination with a binder resin.
As the solvent used for coating the charge transport layer, the same solvent as the charge generation layer can be used, but a solvent that dissolves the charge transport material and the binder resin well is suitable. These solvents may be used alone or in combination of two or more.

(Other additives)
If necessary, a plasticizer, a leveling agent, an antioxidant, a light stabilizer, and an ultraviolet absorber can be added to the charge transport layer. As a plasticizer that can be used in combination with the charge transport layer, those used as a plasticizer for general resins such as dibutyl phthalate and dioctyl phthalate can be used as they are, and the amount used is 0 with respect to 100 parts by mass of the binder resin. About 30 parts by mass is appropriate.
Leveling agents that can be used in combination with the charge transport layer include silicone oils such as dimethyl silicone oil and methylphenyl silicone oil, and polymers or oligomers having a perfluoroalkyl group in the side chain. The amount used is a binder resin. About 0 to 1 part by mass is appropriate for 100 parts by mass.
As the antioxidant, for example, conventionally known materials such as phenolic compounds, paraphenylenediamines, hydroquinones, organic sulfur compounds, organic phosphorus compounds, hindered amines and the like can be used. It is effective for conversion.
A filler can also be added to the charge transport layer. About a filler, the filler kind described in the term of the surface protective layer containing the filler mentioned later and a surface treating agent can be used.
The thickness of the charge transport layer is suitably about 5 to 40 μm, preferably about 10 to 30 μm. The charge transport layer can be formed by the same coating method as that for the charge generation layer. However, when the charge transport layer is the surface layer of the image carrier, undulation is formed on the surface. Therefore, it is preferable that the undulation is formed on the surface of the image carrier by the spray coating method already shown.

<Single-layer photosensitive layer>
A photosensitive layer having a single layer structure is a layer having both a charge generation function and a charge transport function. A charge generation material having a charge generation function, a charge transport material having a charge transport function, and a binder resin are dissolved or dispersed in an appropriate solvent. This can be formed by coating and drying. Moreover, a plasticizer, a leveling agent, etc. can also be added as needed. As the charge generation material dispersion method, the charge generation material, the charge transport material, the plasticizer, and the leveling agent may be the same as those already described in the charge generation layer and the charge transport layer. As the binder resin, in addition to the binder resin previously mentioned in the section of the charge transport layer, the binder resin mentioned in the charge generation layer may be mixed and used. Also, the polymer charge transport materials listed above can be used. The film thickness of the photosensitive layer is suitably about 5 to 30 μm, preferably about 10 to 25 μm. The photosensitive layer can be formed by the same coating method as that for the charge generation layer. However, when the photosensitive layer is the surface layer of the image carrier, undulations are formed on the surface. Therefore, it is preferable to form undulations on the surface of the image carrier by the spray coating method already shown.

<About surface protective layer>
The image carrier of the present invention may be provided with a surface protective layer on the photosensitive layer, and by providing the surface protective layer, it is possible to improve the mechanical durability and the applicability of the lubricating substance. The structure of the surface protective layer may be anything, but examples include a surface protective layer containing a filler, a cross-linked surface protective layer containing a cross-linked resin, and combinations thereof. Further, when the surface protective layer is provided, the surface protective layer becomes the surface layer of the image carrier, and therefore, it is preferable to easily control the waviness shape. Although the specific example of a surface protective layer is shown below, the surface protective layer which can be used for this invention is not limited to this.

(Surface protective layer containing filler)
The mechanical durability of the image carrier is improved by providing a surface protective layer containing a filler on the photosensitive layer. Further, fine irregularities are formed by the filler, the applicability of the lubricating substance is improved, the durability of the image carrier can be increased, and the deterioration of the cleaning blade can be reduced.
As the filler fine particles, organic fillers, carbon fine particles, and inorganic fillers can be used.
Examples of the organic filler material include fluorine resin powder such as polytetrafluoroethylene, silicone resin powder, and carbon fine particles.
The carbon fine particles are particles having a structure mainly composed of carbon. Particles having a structure such as amorphous, diamond, graphite, amorphous carbon, fullerene, zeppelin, carbon nanotube, carbon nanohorn, and the like. Among these structures, particles containing hydrogen-containing diamond-like carbon or amorphous carbon structure have good mechanical and chemical durability. The diamond-like carbon or amorphous carbon film containing hydrogen is a particle in which similar structures such as a diamond structure having an SP3 orbit, a graphite structure having an SP2 orbit, and an amorphous carbon structure are mixed. Diamond-like carbon or amorphous carbon fine particles are not limited to carbon, but may contain other elements such as hydrogen, oxygen, nitrogen, fluorine, boron, phosphorus, chlorine, bromine and iodine. Absent.

Inorganic filler materials include metal powders such as copper, tin, aluminum, and indium, metal oxides such as silicon oxide, tin oxide, zinc oxide, titanium oxide, indium oxide, antimony oxide, and bismuth oxide, and potassium titanate. An inorganic material is mentioned. In particular, it is advantageous to use an inorganic material among them from the viewpoint of the hardness of the filler. In particular, metal oxides are good, and silicon oxide, aluminum oxide, and titanium oxide can be used effectively. Also, fine particles such as colloidal silica and colloidal alumina can be used effectively.
Any type of filler can be used, but it is preferable to use a high-hardness inorganic filler in order to form a stronger film.

  If the concentration of the filler in the surface protective layer is too high, side effects such as an increase in residual potential and a decrease in writing light transmittance may occur. Therefore, it is about 50% by mass or less, preferably about 30% by mass or less, based on the total solid content.

The particle size of the filler is preferably 0.1 μm or more and 1.0 μm or less, and more preferably 0.1 μm or more and 0.5 μm or less in order to form a fine uneven shape. When the particle size is smaller than 0.1 μm, the particle size is too small, so that improvement in mechanical durability cannot be expected, and fine irregularities may not be formed. On the other hand, when the thickness is larger than 1.0 μm, the convex shape due to the filler becomes large, and the behavior of the cleaning blade becomes unstable, which may cause deterioration of the blade and poor cleaning.
In addition, the particle size of the filler in the present invention means an average particle size of primary particles representing the particle group, and is expressed as a number average size. Specifically, it can be obtained by directly cutting the filler or the image carrier containing the filler and directly observing the cross section with an electron microscope or the like.

  Furthermore, these fillers can be surface-treated with at least one kind of surface treatment agent, and it is preferable from the viewpoint of dispersibility of the fillers. Decreasing the dispersibility of the filler not only increases the residual potential, but also decreases the transparency of the coating, causes defects in the coating, and decreases the wear resistance. It can develop into a big problem. As the surface treatment agent, a conventionally used surface treatment agent can be used, but a surface treatment agent capable of maintaining the insulating properties of the filler is preferable.

The surface treatment amount varies depending on the average primary particle size of the filler used, but is preferably 0.1 to 50% by mass, more preferably 5 to 20% by mass with respect to the filler mass. If the surface treatment amount is less than this, the filler dispersion effect cannot be obtained, and if it is too much, the residual potential is significantly increased. These filler materials may be used alone or in combination of two or more.
The filler material can be dispersed by using a conventional method such as a ball mill, attritor, sand mill, or ultrasonic wave together with at least an organic solvent and, if necessary, a dispersant. As the material of the media used, conventionally used media such as zirconia, alumina, and agate can be used, but it is more preferable to use alumina from the viewpoint of filler dispersibility and residual potential reduction effect. Α-type alumina having excellent wear resistance is particularly preferable.
Moreover, the material shown with the said charge transport layer can be used also about binder resin used for a surface protective layer. Moreover, a crosslinked resin can also be used as a binder resin for the surface protective layer. The cross-linked resin will be described in the cross-linking curable surface protective layer described later.

The surface protective layer may contain a charge transport material, and in order to improve the electrical characteristics of the image carrier, it is preferable to contain a charge transport material. As the charge transport material, the materials shown in the charge generation layer can be used.
If necessary, a plasticizer, a leveling agent, an antioxidant, a light stabilizer, an ultraviolet absorber and the like can be added to the surface protective layer. As these additives, the materials shown in the charge transport layer can be used.

The thickness of the surface protective layer is suitably about 0.1 to 10 μm. Furthermore, it is preferable that it is the range of 1.0-8.0 micrometers. When the thickness is less than 0.1 μm, the durability cannot be improved because the film thickness is thin. When the film thickness of the surface protective layer is larger than 10 μm, an increase in residual potential and a decrease in fine dot reproducibility can be considered.
As a film forming method of the surface protective layer, it is preferable to apply by spray coating in order to form undulations. About spray coating conditions, it is preferable to perform coating by the method already shown.

(Crosslinked surface protective layer)
By providing a cross-linked surface protective layer containing a cross-linked resin on the photosensitive layer, the mechanical durability of the film is greatly improved. Further, it is possible to maintain the undulation on the surface of the image carrier for a long period of time, whereby the durability of the image carrier and the vibration of the cleaning blade can be maintained for a long period of time. In an image forming apparatus expected to be used for a long time, it is effective to provide a cross-linked surface protective layer.
A crosslinked resin is a resin obtained by curing one or more polymerizable compounds. Polymerization refers to the former form of polymerization reaction in which the formation reaction of polymer compounds is largely divided into chain polymerization and sequential polymerization, and the reaction proceeds mainly via intermediates such as radicals or ions. This refers to unsaturated polymerization, ring-opening polymerization and isomerization polymerization. The polymerizable compound means a compound having a functional group capable of the above reaction form. In general, curing means that monomers and oligomers having the above functional groups are bonded (for example, shared) between molecules by applying energy such as heat, light such as visible light or ultraviolet light, radiation such as electron beams and γ rays. Reaction) to form a three-dimensional network structure.

Examples of the crosslinked resin include a thermosetting resin that is polymerized by heat, a photocurable resin that is polymerized by light such as ultraviolet rays and visible light, an electron beam curable resin that is polymerized by an electron beam, and the like. Used in combination with a catalyst, a polymerization initiator and the like.
In order to obtain the cross-linked resin, it is necessary that a polymerizable compound (for example, a monomer or an oligomer) has a functional group that causes a polymerization reaction. As the functional group, any functional group that causes a polymerization reaction can be used, but generally, an unsaturated polymerizable functional group or a ring-opening polymerizable functional group is known. This is also effective in the invention. The unsaturated polymerizable functional group is a reaction in which an unsaturated group is polymerized by radicals or ions. For example, a functional group such as C═C, C≡C, C═O, C═N, C≡N Can be mentioned. A ring-opening polymerizable functional group is a reaction in which an unstable cyclic structure having a strain such as a carbocyclic ring, an oxo ring, or a nitrogen heterocycle repeats polymerization at the same time as the ring opening to generate a chain polymer. Most of these act as active species. Examples of these include groups having a carbon-carbon double bond such as acryloyl group, methacryloyl group and vinyl group, groups that cause ring-opening polymerization such as silanol group and cyclic ether group, or reaction of two or more kinds of molecules. Things. Among these polymerizable functional groups, an acryloyloxy group and a methacryloyloxy group are particularly useful as the polymerizable functional group.
Further, in the curing reaction, the larger the number of functional groups in one molecule of the polymerizable compound, the stronger the three-dimensional network structure becomes, and the trifunctional or higher functionality is particularly effective. As a result, the curing density is increased, the hardness is high, and the elasticity is high, which is effective for improving the durability and image quality of the image carrier.

  For the surface protective layer in the present invention, a conventionally known crosslinked resin can be used, and a high effect can be obtained by being cured regardless of the material and means. Examples of the cross-linked resin include phenol resin, epoxy resin, melamine resin, alkyd resin, urethane resin, amino resin, polyimide resin, siloxane resin, acrylic resin, etc., particularly urethane resin, phenol resin, acrylic / methacrylic resin. Etc. are preferably used. Among these, acrylic / methacrylic resins are easy to obtain the effects of the present invention and can be used particularly well. These cross-linked resins are characterized in that they have a three-dimensional network structure and are insoluble in organic solvents. Accordingly, the cured state in the present invention can be determined to be cured if, for example, the film does not dissolve even when an alcoholic organic solvent is attached.

  Furthermore, it is more preferable to use a resin obtained by curing a polymerizable compound having no charge transporting structure and a polymerizable compound having a charge transporting structure for the cross-linked surface protective layer in the present invention. When cured only with a polymerizable compound having no charge transporting structure, there is no function of transporting charges to the surface layer, electrical characteristics are lowered, and image quality tends to be lowered. In order to achieve high image quality, it is preferable to use a resin in which a polymerizable compound having no charge transporting structure and a polymerizable compound having a charge transporting structure are cured.

The number of functional groups of the polymerizable compound (monomer or oligomer) having no charge transport structure is preferably polyfunctional, and more preferably trifunctional or higher. By using a tri- or higher functional polymerizable monomer that does not have a transportable structure, a three-dimensional network structure is developed, and a highly hard and highly elastic cross-linked surface layer having a very high cross-link density is obtained, resulting in high wear resistance. And scratch resistance is achieved. In addition, by using a polymerizable compound having a charge transporting structure, they are simultaneously polymerized and cured in a short time to form a high-hardness cross-linked bond, thereby improving durability. Furthermore, there is less distortion in the cross-linked layer by curing a polymerizable monomer having a charge transporting structure and a trifunctional or higher functional monomer having many reactive functional groups, fast curing speed, and no charge transporting structure. A uniform cross-linked film can be formed. As a result, the unreacted portion of the charge transport material is reduced in the cross-linked surface layer, and the homogeneity inside the cross-linked film is greatly improved. As a result, it is possible to achieve both of improved wear resistance and at the same time stable electrostatic characteristics and an image carrier free of cracks. It can be obtained by ester reaction or transesterification reaction using a certain compound and acrylic acid (salt), acrylic acid halide, or acrylic ester. A compound having three or more methacryloyloxy groups can be obtained in the same manner. Moreover, the polymerizable functional groups in the monomer having three or more polymerizable functional groups may be the same or different.

Specific examples of the trifunctional or higher functional polymerizable compound having no charge transporting structure include the following, but are not limited to these compounds.
That is, as the polymerizable compound used in the present invention, for example, trimethylolpropane triacrylate (TMPTA), trimethylolpropane trimethacrylate, trimethylolpropane alkylene-modified triacrylate, trimethylolpropane ethyleneoxy modification (hereinafter referred to as EO modification). Triacrylate, trimethylolpropane propyleneoxy modified (hereinafter PO modified) triacrylate, trimethylolpropane caprolactone modified triacrylate, trimethylolpropane alkylene modified trimethacrylate, pentaerythritol triacrylate, pentaerythritol tetraacrylate (PETTA), glycerol triacrylate, Glycerol epichlorohydrin modified (hereinafter ECH modified) triacryle Glycerol EO modified triacrylate, glycerol PO modified triacrylate, tris (acryloxyethyl) isocyanurate, dipentaerythritol hexaacrylate (DPHA), dipentaerythritol caprolactone modified hexaacrylate, dipentaerythritol hydroxypentaacrylate, alkylated di Pentaerythritol pentaacrylate, alkylated dipentaerythritol tetraacrylate, alkylated dipentaerythritol triacrylate, dimethylolpropane tetraacrylate (DTMPTA), pentaerythritol ethoxytetraacrylate, EO-modified triacrylate 2, 2, 5, 5 -Tetrahydroxymethylcyclopentanone tetraacrylate Is, it may be used in combination either alone or in combination.

The polymerizable compound having a charge transporting structure in the present invention is a hole transporting structure such as triarylamine, hydrazone, pyrazoline, carbazole, etc., for example, an electron withdrawing property having a condensed polycyclic quinone, diphenoquinone, a cyano group or a nitro group. It is a compound having either or both of electron transport structures such as aromatic rings and having a polymerizable functional group.
Examples of the polymerizable functional group include those described above for the polymerizable compound, and acryloyloxy group and methacryloyloxy group are particularly useful. As the polymerizable compound having a charge transporting structure used in the surface protective layer of the present invention, any number of functional groups can be used, but one functional group is from the viewpoint of stability of electrostatic characteristics and film quality. More preferred. In the case of bifunctional or higher, a plurality of bonds are fixed in the cross-linked structure and the cross-linking density is further increased, but the charge transporting structure is very bulky, which increases the strain of the layer structure and increases the internal stress of the layer. . In addition, the intermediate structure (cation radical) at the time of charge transport cannot be kept stable, and there is a risk that a decrease in sensitivity due to charge trapping and an increase in residual potential are likely to occur.
Specific examples of the polymerizable compound having a charge transport structure include materials described in JP-A No. 2004-302450.

  The polymerizable compound having a charge transport structure used in the present invention is important for imparting the charge transport performance of the surface protective layer, and this component is 20 to 80% by weight, preferably 30 to 70%, based on the surface protective layer. % By weight. If this component is less than 20% by weight, the charge transport performance of the surface protective layer cannot be maintained sufficiently, and deterioration of electrostatic characteristics such as a decrease in sensitivity and an increase in residual potential may be observed with repeated use. On the other hand, when the content is 80% by weight or more, the content of the polymerizable compound having no charge transport structure is decreased, and the crosslink density is decreased, so that high wear resistance and scratch resistance may not be exhibited. The electrical characteristics and abrasion resistance required vary depending on the process used, and the film thickness of the surface protective layer of the image carrier varies accordingly. A weight percent range is most preferred. Although these polymerizable compounds having a charge transporting structure cannot be isolated because they are cured, this method can be quantified as a charge transporting structure using a method such as FT-IR. It can be obtained as the concentration ratio of the charge transport material in the invention.

As described above, a product obtained by curing a trifunctional or higher functional polymerizable compound having no charge transport structure and a polymerizable compound having a monofunctional charge transport structure is particularly effective. It is also possible to use a polymerizable monomer and a polymerizable oligomer, which may be very effective depending on the material. As these polymerizable monomers and oligomers, known ones can be used.
Examples of the monofunctional radical monomer include 2-ethylhexyl acrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, tetrahydrofurfuryl acrylate, 2-ethylhexyl carbitol acrylate, 3-methoxybutyl acrylate, benzyl acrylate, and cyclohexyl acrylate. , Isoamyl acrylate, isobutyl acrylate, methoxytriethylene glycol acrylate, phenoxytetraethylene glycol acrylate, cetyl acrylate, isostearyl acrylate, stearyl acrylate, styrene monomer, and the like.
Examples of the bifunctional polymerizable monomer include 1,3-butanediol diacrylate, 1,4-butanediol diacrylate, 1,4-butanediol dimethacrylate, 1,6-hexanediol diacrylate, and 1,6. -Hexanediol dimethacrylate, diethylene glycol diacrylate, neopentyl glycol diacrylate, bisphenol A-EO modified diacrylate, bisphenol F-EO modified diacrylate, neopentyl glycol diacrylate, and the like.

Examples of the functional monomer include those substituted with fluorine atoms such as octafluoropentyl acrylate, 2-perfluorooctylethyl acrylate, 2-perfluorooctylethyl methacrylate, 2-perfluoroisononylethyl acrylate, No. 60503, JP-B-6-45770, siloxane repeating units: 20-70 acryloyl polydimethylsiloxane ethyl, methacryloyl polydimethylsiloxane ethyl, acryloyl polydimethylsiloxane propyl, acryloyl polydimethylsiloxane butyl, diacryloyl polydimethylsiloxane Examples include vinyl monomers having a polysiloxane group such as diethyl, acrylates and methacrylates.
Examples of the polymerizable oligomer include epoxy acrylate-based, urethane acrylate-based, and polyester acrylate-based oligomers.
Moreover, in order to advance this hardening reaction efficiently as needed, you may contain a polymerization initiator in a protective layer coating liquid.

  As the thermal polymerization initiator, 2,5-dimethylhexane-2,5-dihydroperoxide, dicumyl peroxide, benzoyl peroxide, t-butylcumyl peroxide, 2,5-dimethyl-2,5-di ( Peroxybenzoyl) hexyne-3, di-t-butyl peroxide, t-butyl hydroperoxide, cumene hydroperoxide, lauroyl peroxide, 2,2-bis (4,4-di-t-butylperoxycyclohexyl) B) Peroxide initiators such as propane, azo series such as azobisisobutyronitrile, azobiscyclohexanecarbonitrile, methyl azobisisobutyrate, azobisisobutylamidine hydrochloride, 4,4'-azobis-4-cyanovaleric acid Initiators are mentioned.

As photopolymerization initiators, diethoxyacetophenone, 2,2-dimethoxy-1,2-diphenylethane-1-one, 1-hydroxy-cyclohexyl-phenyl-ketone, 4- (2-hydroxyethoxy) phenyl- (2 -Hydroxy-2-propyl) ketone, 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) butanone-1, 2-hydroxy-2-methyl-1-phenylpropan-1-one, 2- Acetophenone-based or ketal-based photopolymerization initiators such as methyl-2-morpholino (4-methylthiophenyl) propan-1-one, 1-phenyl-1,2-propanedione-2- (o-ethoxycarbonyl) oxime, Benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isobutyl ether Benzoin ether photoinitiators such as benzoin isopropyl ether, benzophenone, 4-hydroxybenzophenone, methyl o-benzoylbenzoate, 2-benzoylnaphthalene, 4-benzoylbiphenyl, 4-benzoylphenyl ether, acrylated benzophenone Benzophenone photopolymerization initiators such as 2-benzoylbenzene, thioxanthones such as 2-isopropylthioxanthone, 2-chlorothioxanthone, 2,4-dimethylthioxanthone, 2,4-diethylthioxanthone, and 2,4-dichlorothioxanthone As photopolymerization initiators and other photopolymerization initiators, ethyl anthraquinone, 2,4,6-trimethylbenzoyldiphenylphosphine oxide, 2,4,6-trimethylbenzoyl Phenylethoxyphosphine oxide, bis (2,4,6-trimethylbenzoyl) phenylphosphine oxide, bis (2,4-dimethoxybenzoyl) -2,4,4-trimethylpentylphosphine oxide, methylphenylglyoxyester, 9, 10 -Phenanthrene, an acridine type compound, a triazine type compound, an imidazole type compound is mentioned. Moreover, what has a photopolymerization acceleration effect can also be used individually or in combination with the said photoinitiator. Examples include triethanolamine, methyldiethanolamine, ethyl 4-dimethylaminobenzoate, isoamyl 4-dimethylaminobenzoate, (2-dimethylamino) ethyl benzoate, 4,4′-dimethylaminobenzophenone, and the like.
These polymerization initiators may be used alone or in combination of two or more. The content of the polymerization initiator is 0.5 to 40 parts by weight, preferably 1 to 20 parts by weight with respect to 100 parts by weight of the total content having polymerizability.

Furthermore, the surface protective layer of the present invention has various plasticizers (added for the purpose of stress relaxation and adhesion improvement), leveling agents, compounds having an alkylamino group, antioxidants, and radical reactivity as necessary. It may contain additives such as low molecular charge transport materials that do not. As these additives, known additives can be used, and as plasticizers, those used in general resins such as dibutyl phthalate and dioctyl phthalate can be used, and the amount used is the total solid content of the coating liquid. To 20 wt% or less, preferably 10 wt% or less.
Further, as leveling agents, silicone oils such as dimethyl silicone oil and methylphenyl silicone oil, polymers or oligomers having a perfluoroalkyl group in the side chain, or leveling agents having a functional group for polymerization are also effective. Can be used. The amount used is suitably 1% by weight or less based on the total solid content of the coating solution. If added in a large amount, the coefficient of friction on the surface of the image carrier is excessively reduced, and the supply amount of the lubricating substance may become unstable.

  In addition, as the compound having an alkylamino group, the materials listed in the charge transport layer can be used effectively. When these materials are added to the surface protective layer located on the outermost surface of the image carrier, a high effect may be obtained. However, if added in a large amount, there is a possibility of causing inhibition of curing, so it is necessary to keep the necessary minimum amount. The addition amount is 3% by weight or less, preferably 2% by weight or less, based on the total solid content of the coating liquid.

As the antioxidant, any conventionally known material can be used. Among them, materials such as phenolic compounds, paraphenylenediamines, hydroquinones, organic sulfur compounds, organic phosphorus compounds, hindered amines, etc. Can be used effectively. Even when an antioxidant is added to the surface protective layer, a high effect may be obtained. However, addition of a large amount may cause inhibition of curing or a significant increase in residual potential. The addition amount is 3% by weight or less, preferably 2% by weight or less, based on the total solid content of the coating liquid.
It is also possible to add a filler to the surface protective layer of the present invention. By adding fillers to the cross-linked resin, the mechanical durability of the image carrier is dramatically improved, the undulation of the image carrier is maintained for a long period of time, and the applicability of the lubricating material is improved to improve the cleaning blade. It is possible to reduce deterioration and maintain high image quality over a long period of time. As for the type of filler, the materials already shown can be applied to the crosslinked resin.

The surface protective layer of the present invention is formed by applying and curing a surface protective layer coating solution containing a monomer before crosslinking on the charge transport layer. In the case where the polymerizable compound is a liquid, such a coating liquid can be applied by dissolving other components in the liquid, but if necessary, it is diluted with a solvent and applied.
Solvents used at this time include alcohols such as methanol, ethanol, propanol and butanol, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclopentanone and cyclohexanone, esters such as ethyl acetate and butyl acetate, tetrahydrofuran, Examples include ethers such as dioxane and propyl ether, halogens such as dichloromethane, dichloroethane, trichloroethane and chlorobenzene, aromatics such as benzene, toluene and xylene, and cellosolves such as methyl cellosolve, ethyl cellosolve and cellosolve acetate. These solvents may be used alone or in combination of two or more. The dilution ratio with the solvent varies depending on the solubility of the composition, the coating method, and the target film thickness, and is arbitrary. In order to form undulations, the coating method is preferably applied by spray coating as already shown.

  In the present invention, after applying the surface protective layer coating solution, energy is applied from the outside to be cured to form a protective layer. The external energy used at this time includes heat, light, and radiation. The heat energy is applied by heating from the coating surface side or the support side using a gas such as air or nitrogen, steam, various heat media, infrared rays, or electromagnetic waves. The heating temperature is preferably 100 ° C. or more and 170 ° C. or less, and if it is less than 100 ° C., the reaction rate is slow and the curing reaction is not completely completed. When the temperature is higher than 170 ° C., the curing reaction proceeds non-uniformly, and large distortion, a large number of unreacted residues, and reaction termination terminals are generated in the surface protective layer. In order to advance the curing reaction uniformly, it is also effective to complete the reaction by heating at a relatively low temperature of less than 100 ° C. and then heating to 100 ° C. or more.

UV light source such as high-pressure mercury lamp or metal halide lamp, which mainly has ultraviolet light emission wavelength, can be used as light energy, but it is also possible to select visible light source according to the absorption wavelength of polymerizable substances and photopolymerization initiator It is. Irradiation light amount is 50 mW / cm ² or more, preferably 1000 mW / cm ² or less, it takes time for the curing reaction is less than 50 mW / cm ^2. If it is higher than 1000 mW / cm ^2, the progress of the reaction becomes non-uniform, and local flaws are generated on the surface of the surface protective layer, and many unreacted residues and reaction termination ends are generated. In addition, internal stress increases due to rapid crosslinking, which causes cracks and film peeling. Examples of radiation energy include those using electron beams. Among these energies, those using heat and light energy are useful because of the ease of reaction rate control and the simplicity of the apparatus.

  The film thickness of the cross-linked surface protective layer is preferably 1.0 μm or more and 8.0 μm or less, more preferably 2.0 μm or more and 6.0 μm or less. If the film thickness is thicker than this, cracks and film peeling are likely to occur as described above, the residual potential rises significantly, and the surface shape becomes difficult to control due to the occurrence of coating film defects. There is a possibility that the effects of the invention cannot be fully exhibited. On the other hand, when the film thickness is thinner than this, it is difficult to obtain the surface shape of the present invention, and in some cases, a coating film defect may easily occur. In addition, if the thickness of the surface protective layer is extremely thin, a region that is not sufficiently covered by the surface protective layer may appear in the lower limit region of the surface roughness, and the effects of the present invention may not be obtained. is there.

<Tandem type image forming apparatus>
The image forming apparatus of the present invention has high wear resistance and scratch resistance of the image bearing member, improved toner transferability and cleaning properties, and suppression of filming. An effect can be obtained. In this respect, it is suitable for printing an image-based document, that is, a full-color image, not a character-based document. In particular, a tandem type image forming apparatus that outputs a full color image with a plurality of image carriers by reducing the difference between the image carriers due to a marked increase in wear resistance and scratch resistance of the image carriers. Used effectively.
The tandem-type image forming apparatus includes the same number of image carriers as the developing units that hold the toners of a plurality of colors independently, thereby processing each color development independently and in parallel. The apparatus then forms a full-color image by superimposing the toner images of the respective colors. Specifically, it is provided with a developing unit and an image carrier of at least four colors of yellow (Y), magenta (M), cyan (C), and black (K) required for full color printing. Compared to the conventional single drum system, which is output by repeating this process, full-color printing is realized at an extremely high speed.

FIG. 7 is a typical schematic diagram for explaining a tandem full-color image forming apparatus according to the present invention. In FIG. 7, reference numerals (1C, 1M, 1Y, 1K) denote drum-shaped image carriers. This image carrier (1C, 1M, 1Y, 1K) rotates in the direction of the arrow in the figure, and therearound charging means (2C, 2M, 2Y, 2K), developing means (4C, 4M, 4Y, 4K) and cleaning means (5C, 5M, 5Y, 5K) are arranged.
Laser light (3C, 3M, 3Y, 3K) from an exposure unit (not shown) from the back side of the image carrier between the charging unit (2C, 2M, 2Y, 2K) and the developing unit (4C, 4M, 4Y, 4K). ) And an electrostatic latent image is formed on the image carrier (1C, 1M, 1Y, 1K). Then, four image forming elements (6C, 6M, 6Y, 6K) centering on such image carriers (1C, 1M, 1Y, 1K) are placed on the transfer conveyance belt (10) as transfer material conveyance means. Are juxtaposed along. The transfer conveyance belt (10) is an image carrier between the developing means (4C, 4M, 4Y, 4K) and the cleaning means (5C, 5M, 5Y, 5K) of each image forming unit (6C, 6M, 6Y, 6K). (1C, 1M, 1Y, 1K), and a transfer brush (11C, 11M, 11Y, 11K) is arranged. Each image forming element (6C, 6M, 6Y, 6K) is different in the color of the toner inside the developing device, and the others are the same in configuration.

  In the full-color image forming apparatus having the configuration shown in FIG. 7, the image forming operation is performed as follows. First, in each image forming element (6C, 6M, 6Y, 6K), the charging means (2C, 2M) in which the image carrier (1C, 1M, 1Y, 1K) rotates in the direction of the arrow (the direction along with the image carrier). 2Y, 2K), and then electrostatic light corresponding to the image of each color to be created by laser light (3C, 3M, 3Y, 3K) by an exposure unit (not shown) arranged outside the image carrier. A latent image is formed. Next, the electrostatic latent image is developed by developing means (4C, 4M, 4Y, 4K) to form a toner image. Developing means (4C, 4M, 4Y, 4K) are developing means for developing with toners of C (cyan), M (magenta), Y (yellow), and K (black), respectively, and four image carriers (1C). 1M, 1Y, 1K) toner images of respective colors are superimposed on the transfer paper. The transfer paper (7) is fed out from the tray by the paper feed roller (8), temporarily stopped by the pair of registration rollers (9), and the transfer and conveyance belt (10) in synchronism with the image formation on the image carrier. Sent to. The transfer paper (7) held on the transfer conveyance belt (10) is conveyed, and the toner images of each color are transferred at contact positions (transfer portions) with the respective image carriers (1C, 1M, 1Y, 1K). Done.

  The toner image on the image carrier is transferred by an electric field formed by a potential difference between the transfer bias applied to the transfer brush (11C, 11M, 11Y, 11K) and the image carrier (1C, 1M, 1Y, 1K). Transferred onto paper (7). Then, the recording paper (7) on which the toner images of four colors are superimposed through the four transfer portions is conveyed to the fixing device (12), where the toner is fixed, and is discharged to a paper discharge portion (not shown). Further, residual toner that is not transferred by the transfer unit and remains on each image carrier (1C, 1M, 1Y, 1K) is collected by a cleaning device (5C, 5M, 5Y, 5K).

  In the example of FIG. 7, the image forming elements are arranged in the order of C (cyan), M (magenta), Y (yellow), and K (black) from the upstream side to the downstream side in the transfer paper conveyance direction. However, it is not limited to this order, and the color order is arbitrarily set. Further, when a black-only document is created, it is particularly effective to use the present invention to provide a mechanism that stops the image forming elements (6C, 6M, 6Y) other than black. Further, although the charging means is in contact with the image carrier in FIG. 7, it is possible to use an adjacent gap type roller charging system by providing an appropriate gap (about 10 to 200 μm) between them, which is effective. . Although it is possible to use a corona charging method as the charging means, if a plurality of corona charging methods are installed, the amount of ozone generated becomes very large, and there is a case where a device for airflow design or the like is required.

FIG. 8 is a diagram schematically illustrating the configuration of a revolver type full-color image forming apparatus.
In the image forming apparatus shown in FIG. 8, toners of a plurality of colors are sequentially developed on one photoconductor 1 by switching the operation of each developing device 4. The toner images of the respective colors are transferred onto the intermediate transfer belt 26 so as to be transferred onto the recording paper P conveyed at a predetermined timing. The recording paper P onto which the superimposed images have been transferred is sent to a fixing device (not shown) and fixed, and is discharged to a paper discharge tray (not shown).

<About process cartridges>
The image forming means as described above may be fixedly incorporated in a copying machine, facsimile, or printer, and each image forming element may be incorporated in the apparatus in the form of a process cartridge. . The process cartridge of the present invention has an arithmetic average waviness Wa (μm) obtained from a waviness curve in which the roughness component is cut off by the λc contour curve filter 0.25 mm and the wavelength component longer than the waviness is cut off by the λf contour curve filter 2.5 mm. Having an undulation of 0.050 μm to 0.30 μm and an average length WSm (mm) of contour curve elements of 0.50 mm to 1.50 mm, and a development gap of 0.1 mm The process cartridge is a process cartridge which is integrated with the developing unit having a size of 0.5 mm or less and a cleaning unit having a cleaning blade, and is detachable from the main body of the image forming apparatus. A general example is shown in FIG.

  For example, as shown in FIG. 9, the process cartridge includes a photosensitive member (101), and further includes a charging unit (102), a developing unit (104), and a cleaning unit (107). It has the member of. The process cartridge example of FIG. 1 has a transfer means (106) for transferring the toner image on the developed photoreceptor (101) to the image receiving paper (105).

  FIG. 10 is an image for evaluating a cleaning failure. When a cleaning failure occurs, an abnormal image is generated as streaky dirt due to the toner that has passed through the cleaning blade.

  EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not restrict | limited to a following example. All parts are parts by weight.

<Image carrier production example 1>
Using an undercoating layer coating solution and a charge generation layer coating solution having the following composition on an aluminum cylinder having an outer diameter of 60 mm, the coating is sequentially applied by a dip coating method, followed by drying in an oven. And a 0.2 μm charge generation layer. Next, using the charge transport layer coating liquid 1 having the following composition, a charge transport layer having a thickness of 20 μm is applied on the charge generation layer by a dip coating method, and the charge having the following composition is further formed on the charge transport layer without drying. Using the coating liquid 2 for the transport layer, the charge transport layer was applied by a spray coating method so as to have a film thickness of 5 μm. After spray coating, touch drying was performed for 10 minutes, followed by drying in an oven to form a charge transport layer having a total film thickness of 25 μm, thereby producing an image carrier. The spray coating conditions are shown below. The viscosity of the charge transport layer coating solution 2 measured with a TV-30 viscometer (manufactured by Toki Sangyo Co., Ltd.) was 1.8 mPa · s. The drying conditions for each layer were 120 ° C. and 10 minutes for the undercoat layer, 90 ° C. and 20 minutes for the charge generation layer, and 130 ° C. and 20 minutes for the charge transport layer.

(Coating liquid for undercoat layer)
Titanium oxide A: 70 parts (CR-EL, average primary particle size: about 0.25 μm, manufactured by Ishihara Sangyo Co., Ltd.)
Titanium oxide B: 20 parts (PT-401M, average primary particle size: about 0.07 μm, manufactured by Ishihara Sangyo Co., Ltd.)
Alkyd resin: 14 parts (Beckolite M6401-50, solid content: 50%, manufactured by Dainippon Ink & Chemicals, Inc.)
Melamine resin: 8 parts (L-145-60, solid content: 60%, manufactured by Dainippon Ink & Chemicals, Inc.)
2-butanone: 70 parts

ポリビニルブチラール： ４部
（ＢＸ−１、積水化学工業社製）
２−ブタノン： ４００部
市販のビーズミル分散機に直径０．５ｍｍのＰＳＺボールを用い、ポリビニルブチラールを溶解した２−ブタノン溶液及び上記チタニルフタロシアニンを投入し、ローター回転数１２００ｒｐｍにて３０分間分散を行い、電荷発生層用塗工液を作製した。 (Coating solution for charge generation layer)
Titanylphthalocyanine of the following structural formula (I): 8 parts

Polyvinyl butyral: 4 parts (BX-1, manufactured by Sekisui Chemical Co., Ltd.)
2-butanone: 400 parts Using a PSZ ball having a diameter of 0.5 mm in a commercially available bead mill disperser, the 2-butanone solution in which polyvinyl butyral is dissolved and the above titanyl phthalocyanine are charged, and dispersion is performed at a rotor rotation speed of 1200 rpm for 30 minutes. A charge generation layer coating solution was prepared.

下記構造式（III）の酸化防止剤： １部

テトラヒドロフラン： ８０部
１％シリコーンオイルのテトラヒドロフラン溶液： ０．２部
（ＫＦ５０−１００ＣＳ、信越化学工業製） (Coating liquid 1 for charge transport layer)
Bisphenol Z polycarbonate: 10 parts (Panlite TS-2050, manufactured by Teijin Chemicals)
Low molecular charge transport material of the following structural formula (II): 7 parts

Antioxidant of the following structural formula (III): 1 part

Tetrahydrofuran: 80 parts Tetrahydrofuran solution of 1% silicone oil: 0.2 parts (KF50-100CS, manufactured by Shin-Etsu Chemical Co., Ltd.)

(Charge transport layer coating solution 2)
Bisphenol Z polycarbonate: 10 parts (Panlite TS-2050, manufactured by Teijin Chemicals)
Low molecular charge transport material of structural formula (II): 7 parts Antioxidant of structural formula (III): 1 part Tetrahydrofuran: 470 parts 1% silicone oil in tetrahydrofuran solution: 0.2 part (KF50-100CS, Shin-Etsu Chemical Co., Ltd.) Made)

(Spray coating conditions)
Spray distance: 50mm
Discharge rate: 4cc / min
Spray moving speed: 6mm / s
Drum rotation speed: 140 rpm
Atomization air pressure: 0.5 kgf / cm ²
Atomization air flow rate: 12.5 L / min
Number of coatings: 4 times

<Image carrier production example 2>
An image carrier was produced in the same manner as in Image Carrier Production Example 1 except that the atomizing air pressure under the spray coating conditions was changed to 0.7 kgf / cm ² and the atomizing air flow rate was changed to 13 L / min.

<Image carrier production example 3>
An image carrier was prepared in the same manner as in Image Carrier Production Example 1 except that the atomizing air pressure under spray coating conditions was changed to 0.9 kgf / cm ² and the atomizing air flow rate was changed to 14 L / min.

<Image carrier production example 4>
An image carrier was produced in the same manner as in Image Carrier Production Example 1 except that the atomizing air pressure in the spray coating conditions was changed to 1.2 kgf / cm ² and the atomizing air flow rate was changed to 15.5 L / min. .

<Image carrier production example 5>
An image carrier was produced in the same manner as in Image Carrier Production Example 1 except that the atomizing air pressure under spray coating conditions was changed to 1.5 kgf / cm ² and the atomizing air flow rate was changed to 17 L / min.

<Image Carrier Production Example 6>
The charge generation layer was coated in the same manner as in Image Carrier Production Example 1. Next, using the charge transport layer coating liquid 1 of Production Example 1 of the image carrier, a charge transport layer having a film thickness of 25 μm is applied on the charge generation layer by a dip coating method, and spray coating is not performed. After drying for 20 minutes, an image carrier was produced.

<Image Carrier Production Example 7>
The charge generation layer was coated in the same manner as in Image Carrier Production Example 1. Next, using the charge transport layer coating solution 3 having the following composition, a charge transport layer having a thickness of 20 μm was applied on the charge generation layer by a dip coating method, and the charge having the following composition was further formed thereon without being dried. Using the coating liquid 4 for the transport layer, the charge transport layer was applied by a spray coating method so as to have a film thickness of 5 μm. After spray coating, touch drying was performed for 10 minutes, followed by drying in an oven to form a charge transport layer having a total film thickness of 25 μm, thereby producing an image carrier. The mill base added to the charge transport layer coating solution was prepared by the following method. The spray coating conditions are shown below. The viscosity of the charge transport layer coating solution 4 was 1.9 mPa · s. The drying conditions for each layer were 120 ° C. and 10 minutes for the undercoat layer, 90 ° C. and 20 minutes for the charge generation layer, and 130 ° C. and 20 minutes for the charge transport layer.

(Coating liquid 3 for charge transport layer)
Bisphenol Z polycarbonate: 9 parts (Panlite TS-2050, manufactured by Teijin Chemicals)
Low molecular charge transport material of structural formula (II): 7 parts Antioxidant of structural formula (III): 1 part Tetrahydrofuran: 78 parts 1% silicone oil in tetrahydrofuran: 0.2 parts (KF50-100CS, Shin-Etsu Chemical Co., Ltd.) Made)
Mill base 3 parts

(Charge transport layer coating solution 4)
Bisphenol Z polycarbonate: 9 parts (Panlite TS-2050, manufactured by Teijin Chemicals)
Low molecular charge transport material of structural formula (II): 7 parts Antioxidant of structural formula (III): 1 part Tetrahydrofuran: 468 parts 1% silicone oil in tetrahydrofuran solution: 0.2 part (KF50-100CS, Shin-Etsu Chemical Co., Ltd.) Made)
Mill base 3 parts

(Mill base)
For the mill base, a φ5 mm alumina ball was placed in a 70 cc glass pot, and the following filler, polycarboxylic acid compound, cyclopentanone, and tetrahydrofuran were added. .
Alumina filler: 8 parts (Sumicorundum AA-03, average primary particle size: 0.3 μm, manufactured by Sumitomo Chemical Co., Ltd.)
Polycarboxylic acid compound: 0.2 part (BYK-P104, manufactured by BYK Chemie)
Cyclopentanone: 8 parts Tetrahydrofuran: 12 parts

(Spray coating conditions)
Spray distance: 50mm
Discharge rate: 4cc / min
Spray moving speed: 6mm / s
Drum rotation speed: 140 rpm
Atomization air pressure: 0.5 kgf / cm ²
Atomization air flow rate: 12 L / min
Number of coatings: 4 times

<Image carrier production example 8>
An image carrier was prepared in the same manner as in Image Carrier Production Example 7 except that the atomizing air pressure under the spray coating conditions was changed to 0.7 kgf / cm ² and the atomizing air flow rate was changed to 13 L / min.

<Image Carrier Production Example 9>
An image carrier was produced in the same manner as in Image carrier production example 7 except that the atomizing air pressure under spray coating conditions was changed to 0.9 kgf / cm ² and the atomizing air flow rate was changed to 14 L / min.

<Image Carrier Production Example 10>
An image carrier was produced in the same manner as in Image Carrier Production Example 7 except that the atomizing air pressure under the spray coating conditions was changed to 1.2 kgf / cm ² and the atomizing air flow rate was changed to 15.5 L / min. .

<Image Carrier Production Example 11>
An image carrier was produced in the same manner as in Image carrier production example 7, except that the atomizing air pressure under the spray coating conditions was changed to 1.5 kgf / cm ² and the atomizing air flow rate was changed to 17 L / min.

<Image Carrier Production Example 12>
The charge generation layer was coated in the same manner as in Image Carrier Production Example 3. Next, a charge transport layer having a film thickness of 25 μm was applied on the charge generation layer by a dip coating method using the charge transport layer coating liquid 3 of Image Carrier Production Example 7, and spray coating was not performed. After drying for 20 minutes, an image carrier was produced.

<Image Carrier Production Example 13>
The charge generation layer was coated in the same manner as in Image Carrier Production Example 1. The charge transport layer coating solution was formulated as follows, and applied onto the charge generation layer by a dip coating method. The thickness of the charge transport layer was 20 μm.
(Coating liquid for charge transport layer)
Bisphenol Z polycarbonate: 10 parts (Panlite TS-2050, manufactured by Teijin Chemicals)
Low molecular charge transport material of structural formula (II): 10 parts Antioxidant of structural formula (III): 1 part Tetrahydrofuran: 80 parts Tetrahydrofuran solution of 1% silicone oil: 0.2 part (KF50-100CS, Shin-Etsu Chemical Co., Ltd.) Made)

Next, a surface protective layer coating solution 1 having the following formulation was prepared. For alumina filler, put φ5mm alumina balls in a 70cc glass pot, and then add the following filler, polycarboxylic acid compound, cyclohexanone, and tetrahydrofuran. did. Thereafter, the surface protective layer coating liquid 1 was prepared by mixing the mill base with the other materials of the surface protective layer coating liquid 1. The viscosity of the surface protective layer coating solution 1 was 1.1 mPa · s.
The surface protective layer coating solution 1 was applied on the charge transport layer by a spray coating method so as to have a film thickness of 5 μm. The spray coating conditions are shown below. After coating, finger touch drying was performed for 5 minutes, followed by drying at 150 ° C. for 20 minutes to prepare an image carrier.
(Mill base)
Alumina filler: 8 parts (Sumicorundum AA-03, average primary particle size: 0.3 μm, manufactured by Sumitomo Chemical Co., Ltd.)
Polycarboxylic acid compound: 0.2 part (BYK-P104, manufactured by BYK Chemie)
Cyclohexanone: 8 parts Tetrahydrofuran: 12 parts

(Coating liquid 1 for surface protective layer)
Charge transport material of structural formula (II): 3 parts Bisphenol Z polycarbonate: 4 parts Millbase: 3 parts Tetrahydrofuran: 180 parts Cyclohexanone: 90 parts

(Spray coating conditions)
Spray distance: 50mm
Discharge rate: 6cc / min
Spray moving speed: 6mm / s
Drum rotation speed: 140 rpm
Atomization air pressure: 0.5 kgf / cm ²
Atomization air flow rate: 12 L / min
Number of coatings: 3 times

<Image Carrier Production Example 14>
An image carrier was produced in the same manner as in Image Carrier Production Example 13 except that the atomizing air pressure in the spray coating conditions was changed to 0.6 kgf / cm ² and the atomizing air flow rate was changed to 12.5 L / min. .

<Image Carrier Production Example 15>
An image carrier was produced in the same manner as in Image Carrier Production Example 13 except that the atomizing air pressure under spray coating conditions was changed to 0.9 kgf / cm ² and the atomizing air flow rate was changed to 14 L / min.

<Image Carrier Production Example 16>
An image carrier was produced in the same manner as in Image Carrier Production Example 13 except that the atomizing air pressure under the spray coating conditions was changed to 1.1 kgf / cm ² and the atomizing air flow rate was changed to 15 L / min.

<Image Carrier Production Example 17>
An image carrier was produced in the same manner as in Image carrier production example 13 except that the atomizing air pressure under spray coating conditions was changed to 1.5 kgf / cm ² and the atomizing air flow rate was changed to 17 L / min.

<Image Carrier Production Example 18>
Coating was performed up to the charge transport layer in the same manner as in Image Carrier Production Example 13. Next, 20 parts of tetrahydrofuran and 10 parts of cyclohexanone in the surface protective layer coating solution 1 are prepared to prepare a surface protective layer coating solution 2, and the surface protective layer coating solution 2 is used to form a film by a dip coating method. A surface protective layer having a thickness of 5 μm was applied and dried at 150 ° C. for 20 minutes to prepare an image carrier.

<Image Carrier Production Example 19>
In the same manner as in Image Carrier Production Example 13, coating was performed up to the charge transport layer. Next, a surface protective layer coating solution 3 having the following formulation was prepared and applied on the charge transport layer by a spray coating method so as to have a film thickness of 5 μm. The spray coating conditions are shown below. After coating, finger touch drying was performed for 2 minutes, and UV irradiation was performed for 60 seconds at 600 mW / cm ² in a UV irradiation apparatus manufactured by Fusion. After UV irradiation, drying was performed at 130 ° C. for 20 minutes to prepare an image carrier. The viscosity of the surface protective layer coating solution 1 was 0.9 mPa · s.

電荷輸送性構造を有さない３官能以上の重合性モノマー： １０部
トリメチロールプロパントリアクリレート
（日本化薬製、ＫＡＹＡＲＡＤ
ＴＭＰＴＡ、官能基数：３官能）
光重合開始剤： １部
イルガキュア１８４（日本化薬製、分子量：２０４）
テトラヒドロフラン： １２０部 (Coating liquid 3 for surface protective layer)
Polymerizable compound having a charge transport structure of the following structural formula (IV): 10 parts

Trifunctional or higher polymerizable monomer having no charge transport structure: 10 parts trimethylolpropane triacrylate (manufactured by Nippon Kayaku, KAYARAD
TMPTA, number of functional groups: 3)
Photopolymerization initiator: 1 part Irgacure 184 (manufactured by Nippon Kayaku, molecular weight: 204)
Tetrahydrofuran: 120 parts

(Spray coating conditions)
Spray distance: 50mm
Discharge rate: 4.0 cc / min
Spray moving speed: 6mm / s
Drum rotation speed: 140 rpm
Atomization air pressure: 0.5 kgf / cm ²
Atomization air flow rate: 12 L / min
Number of coatings: 1

<Image Carrier Production Example 20>
An image carrier was produced in the same manner as in Image carrier production example 19 except that the atomizing air pressure in the spray coating conditions was changed to 0.6 kgf / cm ² and the atomizing air flow rate was changed to 12.5 L / min. .

<Image Carrier Production Example 21>
An image carrier was produced in the same manner as in Image Carrier Production Example 19 except that the atomizing air pressure under the spray coating conditions was changed to 1.0 kgf / cm ² and the atomizing air flow rate was changed to 14.5 L / min. .

<Image Carrier Production Example 22>
An image carrier was produced in the same manner as in Image carrier production example 19 except that the atomizing air pressure in the spray coating conditions was changed to 1.2 kgf / cm ² and the atomizing air flow rate was changed to 15.5 L / min. .

<Image Carrier Production Example 23>
An image carrier was produced in the same manner as in Image Carrier Production Example 19 except that the atomizing air pressure under spray coating conditions was changed to 1.5 kgf / cm ² and the atomizing air flow rate was changed to 17 L / min.

<Image Carrier Production Example 24>
Coating was performed up to the charge transport layer in the same manner as in Image Carrier Production Example 19. Next, a surface protective layer coating solution 4 is prepared by using 20 parts of tetrahydrofuran of the surface protective layer coating solution 3 of image carrier production example 19 and this surface protective layer coating solution 4 is used to produce a ring coating method. Then, a surface protective layer having a thickness of 5 μm was applied and dried at 130 ° C. for 20 minutes to prepare an image carrier.

次に下記処方の表面保護層用塗工液５を作製した。アルミナフィラーは、７０ｃｃのガラスポットにφ５ｍｍのアルミナボールを入れ、さらに下記のフィラー、ポリカルボン酸化合物及びシクロペンタノン、テトラヒドロフランを入れ、ボールミルにより２４時間のフィラー分散（１５０ｒｐｍ）を行い、ミルベースを作製した。その後、表面保護層用塗工液５のその他の材料とミルベースを混合することによって表面保護層用塗工液５を作製した。なお表面保護層用塗工液５の粘度は０．９ｍＰａ・ｓであった。 <Image Carrier Production Example 25>
The charge generation layer was coated in the same manner as in Image Carrier Production Example 19. Except for changing the low molecular charge transport material of the charge transport layer to a low molecular charge transport material of the following structural formula (V) and applying a charge transport layer having a thickness of 20 μm, all the same procedures as in Image Carrier Production Example 19 were applied. The coating was applied up to the charge transport layer.

Next, a surface protective layer coating solution 5 having the following formulation was prepared. For alumina filler, put φ5mm alumina balls in a 70cc glass pot, and then add the following filler, polycarboxylic acid compound, cyclopentanone, and tetrahydrofuran, and perform filler dispersion (150rpm) for 24 hours with a ball mill to produce a mill base. did. Thereafter, the surface protective layer coating solution 5 was prepared by mixing the mill base with the other materials of the surface protective layer coating solution 5. The viscosity of the surface protective layer coating solution 5 was 0.9 mPa · s.

(Mill base)
Alumina filler: 8 parts (Sumicorundum AA-03, average primary particle size: 0.3 μm, manufactured by Sumitomo Chemical Co., Ltd.)
Polycarboxylic acid compound: 0.2 part (BYK-P104, manufactured by BYK Chemie)
Cyclopentanone: 8 parts Tetrahydrofuran: 12 parts

電荷輸送性構造を有さない３官能以上の重合性モノマー： １０部
トリメチロールプロパントリアクリレート
（日本化薬製、ＫＡＹＡＲＡＤ ＴＭＰＴＡ、官能基数：３官能）
ミルベース： ３部
光重合開始剤： １部
（イルガキュア１８４ チバスペシャリティケミカルズ製）
テトラヒドロフラン： １２０部
表面保護層用塗工液５を電荷輸送層上にスプレー塗工法により膜厚５μｍとなるように塗工した。スプレー塗工条件は以下に示す。塗工後は２分間の指触乾燥を行い、Ｆｕｓｉｏｎ社製ＵＶ照射装置に６００ｍＷ／ｃｍ^２で６０秒のＵＶ照射を行った。ＵＶ照射後は、１３０℃２０分の乾燥を行い、像担持体を作製した。 (Coating liquid 5 for surface protective layer)
Polymerizable compound having a charge transporting structure represented by the following structural formula (VI): 10 parts

Trifunctional or higher polymerizable monomer having no charge transporting structure: 10 parts Trimethylolpropane triacrylate (manufactured by Nippon Kayaku, KAYARAD TMPTA, functional group number: trifunctional)
Mill base: 3 parts Photopolymerization initiator: 1 part (Irgacure 184, manufactured by Ciba Specialty Chemicals)
Tetrahydrofuran: 120 parts The surface protective layer coating solution 5 was applied on the charge transport layer by a spray coating method so as to have a film thickness of 5 μm. The spray coating conditions are shown below. After coating, finger touch drying was performed for 2 minutes, and UV irradiation was performed for 60 seconds at 600 mW / cm ² in a UV irradiation apparatus manufactured by Fusion. After UV irradiation, drying at 130 ° C. for 20 minutes was performed to produce an image carrier.

(Spray coating conditions)
Spray distance: 50mm
Discharge rate: 4.0 cc / min
Spray moving speed: 6mm / s
Drum rotation speed: 140 rpm
Atomization air pressure: 0.5 kgf / cm ²
Atomization air flow rate: 12 L / min
Number of coatings: 1

<Image Carrier Production Example 26>
An image carrier was produced in the same manner as in Image Carrier Production Example 25 except that the atomizing air pressure under spray coating conditions was changed to 0.6 kgf / cm ² and the atomizing air flow rate was changed to 12.5 L / min. .

<Image Carrier Production Example 27>
An image carrier was produced in the same manner as in Image Carrier Production Example 25 except that the atomizing air pressure under spray coating conditions was changed to 0.9 kgf / cm ² and the atomizing air flow rate was changed to 14 L / min.

<Image Carrier Production Example 28>
An image carrier was produced in the same manner as in Image Carrier Production Example 25 except that the atomizing air pressure in the spray coating conditions was changed to 1.2 kgf / cm ² and the atomizing air flow rate was changed to 15.5 L / min. .

<Image Carrier Production Example 29>
An image carrier was produced in the same manner as in Image Carrier Production Example 25 except that the atomizing air pressure under spray coating conditions was changed to 1.5 kgf / cm ² and the atomizing air flow rate was changed to 17 L / min.

<Image Carrier Production Example 30>
The coating was applied up to the charge transport layer in the same manner as in Image Carrier Production Example 25. Next, a surface protective layer coating solution 6 is prepared by using 20 parts of tetrahydrofuran as the surface protective layer coating solution of Image Carrier Production Example 25, and this surface protective layer coating solution 6 is used to produce a ring coating method. A surface protective layer having a thickness of 5 μm was applied and dried at 130 ° C. for 20 minutes to prepare an image carrier.

<Image Carrier Production Example 31>
Coating was performed up to the charge transport layer in the same manner as in Image Carrier Production Example 6. Next, the surface of the image carrier was polished for 10 minutes with a wrapping film (particle size: 5 microns, manufactured by Sumitomo 3M) to produce an image carrier.

<Image Carrier Production Example 32>
The coating was applied up to the charge transport layer in the same manner as in Image Carrier Production Example 12. Next, the surface of the image carrier was polished for 10 minutes with a wrapping film (particle size: 5 microns, manufactured by Sumitomo 3M) to produce an image carrier.

<Image Carrier Production Example 33>
The surface protective layer was coated in the same manner as in Image Carrier Production Example 18. Next, the surface of the image carrier was polished for 10 minutes with a wrapping film (particle size: 5 microns, manufactured by Sumitomo 3M) to produce an image carrier.

<Image Carrier Production Example 34>
The surface protective layer was coated in the same manner as in Image Carrier Production Example 24. Next, the surface of the image carrier was polished for 10 minutes with a wrapping film (particle size: 5 microns, manufactured by Sumitomo 3M) to produce an image carrier.

<Image Carrier Production Example 35>
The surface protective layer was coated in the same manner as in Image Carrier Production Example 30. Next, the surface of the image carrier was polished for 10 minutes with a wrapping film (particle size: 5 microns, manufactured by Sumitomo 3M) to produce an image carrier.

<Examples 1 to 1615, Comparative Examples 1 to 1920>
The arithmetic average waviness Wa and the average length WSm of the contour curve element of the image carrier produced as described above were measured. As a measuring apparatus, Surfcom 1400D manufactured by Tokyo Seimitsu Co., Ltd. was used, and measurement was performed in accordance with JIS B 0601: 2001 standard. Measurement length is 12.5 mm, reference length is 2.5 mm, contour curve filter λc = 0.25 (mm), contour curve filter λf = 2.5 (mm), measurement speed is 0.60 mm / s, cross section The curve was measured and the least square straight line correction was selected as the slope correction. The measurement is performed in the axial direction of the image carrier, and the measurement is performed for a total of three regions, the central portion of the image carrier, the central region from the upper end to the central portion, and the central region from the lower end to the central portion. A total of 4 points were measured by rotating about 90 ° C. in the direction, 12 points were measured in total, and the average value was adopted. The results are shown in Table 2.

Subsequently, image evaluation was performed on the image carrier. For image evaluation, Ricoh's digital full-color copying machine imagioMPC7500 (tandem) is mounted with an image carrier mounted on a process cartridge and equipped with charging means, exposure means, developing means, transfer means, fixing means, cleaning means, lubricant application means, and static elimination means. Method) was used. As the charging means, a proximity-type charging roller was used. A hard resin roller having a diameter of 10 mm was used as the charging roller, and the gap with the image carrier was adjusted to 50 μm. As the charging condition, an alternating electric field in which a sine wave having a Vpp of 3 kV and a frequency of 1.5 kHz was superimposed as an AC component on a DC component of −600 V was applied. Further, a semiconductor laser having a wavelength of 655 nm is used for the exposure unit, a polymer toner having an average particle size of about 6 μm is used for the toner charged in the development unit, an intermediate transfer belt is used for the transfer unit, and a cleaning blade is used for the cleaning unit. The cleaning blade was in contact with the rotation direction of the image carrier in the counter direction. The material of the cleaning blade was urethane rubber. The developing means was adjusted so that the developing gap was 0.3 mm. Also, as the lubricant application means, a lubricant material solidified in a bar shape is used, and a pressure spring and a fur brush are attached as shown in FIG. 7, and the lubricant material is scraped off by the fur brush, and the surface of the image carrier It was set as the structure supplied to. Further, a lubricant film forming blade was provided as a film forming member so that the lubricating material was uniformly applied to the surface of the image carrier after the lubricating material adhered to the surface of the image carrier. The blade for forming the lubricant film was in contact with the rotation direction of the image carrier in the trailing direction (non-counter direction). The material for the blade for forming the lubricant film was urethane rubber. Zinc stearate was used as the lubricating material.
In this evaluation, the cleaning blade and the lubricant applying blade were used after passing 100,000 sheets and deteriorated.

Image evaluation was performed in a normal temperature and humidity environment (23 ° C. and 55% RH), 20,000 sheets were passed (full color, A4, image area ratio 5%), and images after 10,000 sheets and 20,000 sheets were passed. Outputs were made and evaluated.
As for the cleaning failure, an A3 image as shown in FIG. 9 was output, and streaks caused by the cleaning failure were evaluated. The evaluation criteria are shown in Table 1.
For density reduction, an A3 image with an image area ratio of 100% is output. A total of 18 image densities of 3 points in the main scanning direction and 6 points in the sub-scanning direction of the A3 image were measured, and the average value was evaluated for the image density. X-Lite 938 (Amtech Co., Ltd.) was used for image density measurement.
For density unevenness, output a 2-dot halftone A3 image, measure the image density of a total of 18 points, 3 points in the main scanning direction and 6 points in the sub-scanning direction of the A3 image, and evaluate the difference between the maximum and minimum image density did.
The evaluation results are shown in Table 2.

  In Examples 1 to 15 in which the arithmetic average waviness Wa and the average length WSm of the contour curve elements are within the scope of the present invention, there was no cleaning failure and no decrease in density was observed. On the other hand, Comparative Examples 1 to 20 in which Wa and WSm are outside the scope of the present invention caused a cleaning failure in the image evaluation after the paper was passed. In Comparative Examples 1 to 20, since the lubricating substance was mixed in the developing device after the paper was passed, the developing ability was lowered and the density was lowered.

<Example 16>
Evaluations were made in the same manner as above except that the image carrier of Image Carrier Production Example 3 was used and the development gap of the above apparatus was 0.1 mm. The evaluation results are shown in Table 3.

<Example 17>
Evaluations were made in the same manner as above except that the image carrier of Image Carrier Production Example 3 was used and the development gap of the above apparatus was 0.2 mm. The evaluation results are shown in Table 3.

<Example 18>
Evaluations were made in the same manner as above except that the image carrier of Image Carrier Production Example 3 was used and the development gap of the above apparatus was 0.4 mm. The evaluation results are shown in Table 3.

<Example 19>
Evaluations were made in the same manner as described above except that the image carrier of Image Carrier Production Example 3 was used and the development gap of the above apparatus was 0.5 mm. The evaluation results are shown in Table 3.

<Comparative Example 21>
Evaluations were made in the same manner as described above except that the image carrier of Image Carrier Production Example 3 was used and the development gap of the above apparatus was 0.6 mm. The evaluation results are shown in Table 3.

<Comparative Example 22>
Evaluation was carried out in the same manner as described above except that the image carrier of Image Carrier Production Example 3 was used and the development gap of the above apparatus was 0.7 mm. The evaluation results are shown in Table 3.

<Comparative Example 23>
Evaluations were made in the same manner as described above except that the image carrier of Image Carrier Production Example 3 was used, the development gap of the above apparatus was 0.3 mm, and the lubricating substance coating apparatus was removed. The evaluation results are shown in Table 3.

<Comparative Example 24>
Evaluations were made in the same manner as described above except that the image carrier of Image Carrier Production Example 3 was used, the development gap of the above apparatus was 0.5 mm, and the lubricating substance coating apparatus was removed. The evaluation results are shown in Table 3.

<Comparative Example 25>
Evaluations were made in the same manner as described above except that the image carrier of Image Carrier Production Example 3 was used, the development gap of the above apparatus was 0.6 mm, and the lubricating substance coating apparatus was removed. The evaluation results are shown in Table 3.

<Example 20>
Evaluations were made in the same manner as above except that the image carrier of Image Carrier Production Example 27 was used and the development gap of the above apparatus was 0.2 mm. The evaluation results are shown in Table 3.

<Example 21>
Evaluations were made in the same manner as above except that the image carrier of Image Carrier Production Example 27 was used and the development gap of the above apparatus was 0.4 mm. The evaluation results are shown in Table 3.

<Example 22>
Evaluations were made in the same manner as above except that the image carrier of Image Carrier Production Example 27 was used and the development gap of the above apparatus was 0.5 mm. The evaluation results are shown in Table 3.

<Comparative Example 26>
Evaluations were made in the same manner as above except that the image carrier of Image Carrier Production Example 27 was used and the development gap of the above apparatus was 0.6 mm. The evaluation results are shown in Table 3.

  In Examples 16 to 22 in which the development gap was 0.1 mm or more and 0.5 mm or less, the image density was good and the density unevenness was good even after the paper was passed. On the other hand, Comparative Examples 21, 22, and 26 having a developing gap larger than 0.5 mm have low developing ability, causing density reduction and density unevenness. Further, Comparative Examples 23 to 25 to which no lubricating substance was applied had a cleaning failure.

  The image forming apparatus of the present invention stabilizes the behavior of the blade even when a deteriorated cleaning blade or lubricant film forming blade is used over a long period of time, and prevents the solid lubricant from slipping through. I can. As a result, the developing gap can be narrowed, the developing ability can be improved, and high image quality can be realized. Therefore, the developing gap can be suitably used as an electrophotographic copying machine, a laser printer, a facsimile or the like. .

(Figure 1)
1 Image carrier (photoreceptor)
2 Charging means 2a Charging roller 3 Latent image forming device (exposure device)
DESCRIPTION OF SYMBOLS 4 Developing apparatus 5 Transfer apparatus 6 Fixing apparatus 8 Cleaning apparatus 9 Static elimination apparatus 10 Transfer material conveyance path 30 Lubricant application apparatus 31 Fur brush (lubricant substance application means)
32 Lubricating substance 33 Pressurizing spring (pressing force applying mechanism)

(Figures 2-4)
201 conductive support 202 photosensitive layer 203 charge generation layer 204 charge transport layer 205 surface protective layer A spray gun B substrate

(Fig. 5)
1 Image carrier (photoreceptor)
4 Developing device 52 Developing roller 53 Doctor blade 54 Agitating screw 55 Toner replenishing roller 56 Developer agitating tank 57 Toner accommodating tank X Developing gap

(Fig. 6)
DESCRIPTION OF SYMBOLS 1 Image carrier 8 Cleaning device 8a Cleaning blade 8b Cleaning blade pressing mechanism 20 Lubricant substance (protective agent) supply device 21 Lubricant substance (protective agent)
22 Lubricating substance (protective agent) supply member (fur brush)
23 Pressurizing mechanism (Pressure spring)
24 Lubricant film coating mechanism 24a Blade 24b Blade support 24c Energizing means (coil spring) of the coating mechanism

(Fig. 7)
1C, 1M, 1Y, 1K Image carrier 2C, 2M, 2Y, 2K Charging means 3C, 3M, 3Y, 3K Laser light 4C, 4M, 4Y, 4K Developing means 5C, 5M, 5Y, 5K Cleaning means 6C, 6M, 6Y, 6K Image forming elements 11C, 11M, 11Y, 11K Transfer brush 12 Fixing device 13 Transfer paper 14 Paper feed roller 15 Registration roller 16 Transfer conveyance belt

(Fig. 8)
1 Image carrier (photoreceptor)
2 Latent image former (exposure device)
4 Developing Device 6 Cleaning Unit 7 Charging Unit 26 Intermediate Transfer Belt 28 Transfer Roller

(Fig. 9)
DESCRIPTION OF SYMBOLS 100 Image forming apparatus 101 Photoconductor 102 Charging means 103 Exposure means 104 Developing means 105 Image receiving paper 107 Cleaning means 106 Transfer means

JP 2007-79244 A Japanese Patent Laid-Open No. 02-101488

Claims (7)

  An image bearing member; an electrostatic latent image forming unit that forms an electrostatic latent image on the image carrier; a developing unit that develops the electrostatic latent image with toner to form a visible image; An image having at least transfer means for transferring a visual image to a recording medium, cleaning means for cleaning residual deposits on the surface of the image carrier after transfer, and lubricant application means for applying a lubricant to the surface of the image carrier. In the forming apparatus, the image carrier has an arithmetic surface obtained from a wavy curve obtained by blocking a roughness component on the surface with a λc contour curve filter of 0.25 mm and blocking a wavelength component longer than the waviness with a λf contour curve filter of 2.5 mm. An average waviness Wa (μm) is 0.050 μm or more and 0.30 μm or less, and an average length WSm (mm) of a contour curve element is waviness having a waviness of 0.50 mm or more and 1.50 mm or less, The development The means has a developing means having a development gap of 0.1 mm or more and 0.5 mm or less, and the cleaning means or the lubricant applying means has a cleaning blade and / or a lubricant film forming blade. Forming equipment.   The image forming apparatus according to claim 1, wherein the surface layer of the image carrier contains a filler.   The image forming apparatus according to claim 1, wherein the surface layer of the image carrier is a cross-linked surface layer.   The image forming apparatus according to claim 1, wherein the surface layer of the image carrier is a cross-linked surface layer and contains a filler.   The cross-linked surface layer contains a cross-linked product composed of a polymerizable compound having a charge transporting structure and a tri- or higher functional polymerizable monomer not having a charge transporting structure. 5. The image forming apparatus according to 4.   The image forming apparatus according to claim 1, wherein the lubricating substance contains a fatty acid metal salt. The image forming apparatus according to claim 1, further comprising: an image carrier and an electrostatic latent image forming unit, an exposure unit, a developing unit, a transfer unit, and a cleaning unit. A process cartridge that can be attached to and detached from the image carrier, wherein the surface of the image carrier blocks a roughness component with a λc contour curve filter of 0.25 mm, and a wavelength component longer than the waviness with a λf contour curve filter of 2.5 mm. An undulation in which the arithmetic average undulation Wa (μm) obtained from the undulation curve is 0.050 μm or more and 0.30 μm or less and the average length WSm (mm) of the contour curve element is 0.50 mm or more and 1.50 mm or less. A process cartridge for an image forming apparatus, wherein the image carrier is a held image carrier.

Images