JP4230894B2 - Image forming apparatus - Google Patents

Description

  The present invention includes a titanyl phthalocyanine crystal having at least a specific crystal type and a specific particle size, in which an electric field strength of 30 V / μm or more is applied to the photoconductor by a scorotron charging method, writing having a resolution of 600 dpi or more is performed. The present invention relates to an image forming apparatus using an electrophotographic photosensitive member in which a charge generating layer and a charge transporting layer are sequentially laminated, and operated at a photosensitive member linear velocity of 300 mm / sec or more.

  In recent years, there has been a remarkable development of information processing system machines using electrophotography. In particular, an optical printer that converts information into a digital signal and records information by light is markedly improved in print quality and reliability. This digital recording technique is applied not only to printers but also to ordinary copying machines, and so-called digital copying machines have been developed. In addition, since a variety of information processing functions are added to a conventional copying machine equipped with this digital recording technology for analog copying, it is expected that its demand will increase further in the future. In addition, with the spread of personal computers and the improvement in performance, the progress of digital color printers for performing color output of images and documents is rapidly progressing.

In recent years, printers and copiers have been required to have higher speeds and higher image quality, but there are two major flows. One is a method of speeding up as much as possible while proceeding with downsizing, and the other is a method of using a large-diameter photosensitive member to increase the photosensitive member linear velocity (process linear velocity).
Since the former does not make the diameter of the photosensitive member so large and the apparatus is preferentially designed to reduce the size of the apparatus, there is a limit to speeding up and the life of the photosensitive member is also limited. The latter uses a large-diameter photoconductor and increases the linear velocity of the photoconductor as much as possible in order to achieve a printing speed of about 100 sheets / min. High durability is achieved by substantially reducing the rotational speed of the photosensitive member.

  As a charging method in such a system using a photoconductor having a high linear velocity and a large diameter, a method called a corotron using a metal wire or a scorotron method is used. In particular, in an apparatus using an organic photoreceptor (OPC), since negative charging is usually performed, a scorotron system having a grid is used from the viewpoint of charging stability. Since such a wire-type charging member has a large distance between the charging member and the photosensitive member, it is necessary to increase the applied bias, and it is a contact-type charging member having a roller shape and a form in contact with the photosensitive member. Compared to this, there is a problem that the electric power used is large and the generation amount of oxidizing gases such as ozone and NOx is large. However, the roller-type charging member has problems such that charging performance cannot be followed when high-speed charging is performed, and the reliability of the system cannot be ensured because the roller life is short. Therefore, in an image forming apparatus that operates at a photosensitive member (process) linear velocity of 300 mm / sec or more, it is necessary to make full use of a scorotron charging member.

  For the problem of speeding up, a photoconductor having high sensitivity and high speed response has been used. Usually, an LED of 780 nm LD or near 760 nm is used as a light source, and a corresponding photoconductor (charge generation material) has a diffraction peak (± 0. 0) with respect to a characteristic X-ray (wavelength 1.542Å) of CuKα. 2 °), it is known to use a titanyl phthalocyanine crystal having a maximum diffraction peak at least 27.2 °.

  This specific crystal type has a very high carrier generation function and can be effectively used as a charge generation material for a photoreceptor for a high-speed image forming apparatus. However, this crystal type has a problem that its stability as a crystal is low, and it is easy to undergo a crystal transition against mechanical stress such as dispersion, and thermal stress. Compared to the above, the sensitivity is very low, and when a part of the crystal undergoes crystal transition, a sufficient photocarrier generation function cannot be exhibited. In addition, there is also a problem that abnormal images called “dirt images” that are problems inherent to negative / positive development are likely to occur during repeated use of the photoreceptor.

  In addition, since the frequency of outputting images has increased significantly, it has become an important issue to improve the image quality of the apparatus. In order to achieve high image quality, (i) an electrostatic latent image on the photosensitive member formed by the charging unit and exposure unit is formed as a high-density image, and (ii) a subsequent developing unit There are three problems: to form a toner image faithfully to the electrostatic latent image, and (iii) to accurately transfer the toner image on the photoconductor to the transfer paper.

  As means for solving these problems, (i) a method of forming an electrostatic latent image by high-density writing using a small-diameter beam as an exposure means can be cited. Optical carriers generated in the layer spread due to Coulomb repulsion, and dots having a size corresponding to the beam diameter cannot be formed. (Ii) There is a method of forming a toner image faithful to the electrostatic latent image on the photosensitive member by reducing the toner particle size in the developing means. However, if the surface potential of the photosensitive member is low, the developing efficiency decreases. In other words, the dots are scattered and dots scattered with respect to the dots of the electrostatic latent image are formed. (Iii) Increasing the gap electric field strength in the transfer means can increase the transfer efficiency and faithfully transfer the toner image on the photoconductor to the transfer paper. However, if the transfer electric field strength is increased, a discharge occurs. In some cases, transfer dust may occur and fatigue of the electrical characteristics of the photoreceptor may be promoted.

  Among these, the increase in the photoreceptor surface potential (electric field strength) particularly in (i) and (ii) is caused by the diffraction peak (± 0.2 °) at the Bragg angle 2θ with respect to the characteristic X-ray (wavelength 1.542 mm) of the CuKα. ), When a photoreceptor using a titanyl phthalocyanine crystal having a maximum diffraction peak of at least 27.2 ° is repeatedly used, it causes an abnormal image called “dirt”.

FIG. 1 shows how dots are formed with respect to the electric field strength (photoconductor surface potential / photosensitive layer film thickness) applied to the photoconductor (writing is performed at 1200 dpi). As shown in FIG. 1, in order to faithfully reproduce small-diameter dots, the electric field strength needs to be set higher. FIG. 2 shows the change in the soiling rank with respect to the electric field intensity. The background dirt rank referred to here indicates the degree of background dirt, and the greater the numerical value, the better the degree of background dirt (the less frequently the background dirt is generated). As can be seen from FIGS. 1 and 2, there is a trade-off relationship between the two in terms of electric field strength.
In order to avoid scumming, a system is generally used in which the electric field strength of the photosensitive member is used at 30 V / μm or less and the reproduction of small-diameter dots is somewhat sacrificed. For example, Japanese Patent Laid-Open No. 2001-154379 (Patent Document 1) describes that the electric field strength of a photoreceptor is used at 12 to 40 V / μm in order to achieve both reproducibility of background stains and fine lines. However, when the resolution of the writing light is increased, the writing dots cannot be developed with good reproducibility unless this lower limit is set higher.

In addition, the upper limit value of the electric field strength varies depending on the material (mainly charge generation material) constituting the photoconductor as to the soiling of the photoconductor. A titanyl phthalocyanine crystal having a maximum diffraction peak at 27.2 ° as a diffraction peak (± 0.2 °) with a Bragg angle 2θ with respect to the characteristic X-ray (wavelength 1.542 mm) of the CuKα is very sensitive. However, it has a disadvantage that it is weak against soiling and is actually used only at an electric field strength of about 30 V / μm or less as described above.
The photocarrier generation efficiency (capability) of the titanyl phthalocyanine crystal depends on the electric field strength, and the carrier generation efficiency is extremely lowered as the electric field is lowered. For this reason, in an actual system, the advantage of the specific high sensitivity in the said titanyl phthalocyanine crystal cannot be fully utilized.
Such a problem is a phenomenon that does not cause much problem with low-resolution (400 dpi or less) writing light, but is a problem that appears prominently in recent high-resolution writing (600 dpi or more, finer writing is 1200 dpi or more). is there.

JP 2001-154379 A

Therefore, an object of the present invention is to provide an image forming apparatus that outputs a stable and high-resolution image without occurrence of abnormal images when repeatedly used at high speed.
Specifically, in order to form a high-quality image at a photoconductor linear speed of 300 mm / sec or higher, the photoconductor is charged so that an electric field strength of 30 V / μm or more is formed by a scorotron charging member. In addition, in an image forming apparatus that forms an electrostatic latent image by performing writing with a writing light source of 600 dpi or more, by using a photoconductor containing a titanyl phthalocyanine crystal of a specific crystal type, high sensitivity inherent to titanyl phthalocyanine It is an object of the present invention to provide an image forming apparatus capable of maintaining high-speed and high-speed image output.

  The inventors of the present invention have made various studies in order to output a high-definition image even in repeated use in a small high-speed digital electrophotographic apparatus. As a result, the photosensitive member linear velocity is 300 mm / sec or more, and the scorotron type Charging is performed by the charging member so that the electric field strength applied to the photosensitive member is 30 V / μm or more, writing with a resolution of 600 dpi or more is performed, and the electrophotographic photosensitive member generates at least charge on the conductive support. An electrophotographic photosensitive member in which a charge transport layer and a charge transport layer are sequentially laminated, and a diffraction peak (± 0.2 °) with a Bragg angle 2θ with respect to a characteristic X-ray (wavelength 1.542 mm) of CuKα in the charge generation layer Having a maximum diffraction peak at least 27.2 °, and further having main peaks at 9.4 °, 9.6 °, and 24.0 °, and the lowest diffraction peak. Of the primary particles having a peak at 7.3 ° and having no peak between the 7.3 ° peak and the 9.4 ° peak, and further having a peak at 26.3 °. It has been found that the above problems can be solved by including titanyl phthalocyanine crystals having an average particle size of less than 0.25 μm.

  Such a charge intensity of 30 V / μm or more applied to the photoconductor is larger than a general electric field intensity in electrophotography, and can be more effective in a high-speed digital electrophotographic apparatus that performs high-resolution writing. It is. Although the detailed reason for the effect of the present invention is not clear, as a result of our investigation, the titanyl used in the present invention has a maximum diffraction peak at 27.2 ° as compared with other titanyl phthalocyanine crystals known so far. It is presumed that it originates from the high chemical stability of phthalocyanine crystals and is due to the reduction in the occurrence of soiling.

By the way, it is already known that the resolution is improved by reducing the beam of writing light and reducing the dots formed. In addition, by increasing the voltage applied to the photoconductor to increase the electric field strength applied to the photoconductor, the linearity of movement of the photocarrier generated inside the photoconductor is increased, and the diffusion of dots in the electrostatic latent image is reduced. It is already known to hold down. If these can be combined, a small-diameter dot (a group of photocarriers) is formed inside the photoconductor, and the electric lines of force between the electrode (support) and the photoconductor surface are strengthened, thereby holding the photocarrier. By suppressing the Coulomb repulsion and moving the optical carrier along the lines of electric force, the shape of the dot written by the small-diameter beam itself can be formed as a photoconductor surface potential profile (dot of electrostatic latent image).
However, an increase in the electric field strength applied to the photosensitive member promotes charge injection from the support to the photosensitive layer and promotion of generation of heat carriers in the photosensitive layer, and as a result promotes the occurrence of soiling.

  These phenomena are generally remarkable when a charge generation material having high photocarrier generation efficiency is used, and the diffraction peak (±±) of the Bragg angle 2θ with respect to the characteristic X-ray (wavelength 1.542Å) of CuKα described above. In the case of using a titanyl phthalocyanine crystal having a maximum diffraction peak of at least 27.2 °, it is actually used in a region where the electric field strength is about 30 V / μm or less. .

  As described above, an effective means for controlling the process has been developed, but an effective photoconductor that takes advantage of the feature has not been developed. Therefore, a high electric field strength cannot be applied to improve the image quality. The current problem is that the electrostatic latent image that is faithful to the writing dots on the photoconductor and the toner development that is faithful to the electrostatic latent image remain, but the present invention solves this problem. ing. According to this invention, the said subject is achieved by following (1)-(14).

(1) An image comprising at least a scorotron charging means, an exposure means having a resolution of 600 dpi or higher, a developing means, a transfer means, and an electrophotographic photosensitive member, and operated at a photosensitive member linear velocity of 300 mm / sec or higher. In the forming apparatus, the absolute value of the electric field strength applied to the electrophotographic photosensitive member from the charging means defined as follows is 30 (V / μm) or more, and the electrophotographic photosensitive member is a conductive support. An electrophotographic photosensitive member in which at least a charge generation layer and a charge transport layer are sequentially laminated thereon, and a diffraction peak (± 0) with a Bragg angle 2θ with respect to a characteristic X-ray (wavelength 1.542Å) of CuKα in the charge generation layer. .2 °) has a maximum diffraction peak at least 27.2 °, and further has major peaks at 9.4 °, 9.6 °, and 24.0 °, and the lowest diffraction peak. As An average size of primary particles having a peak at .3 °, no peak between the peak at 7.3 ° and the peak at 9.4 °, and further having a peak at 26.3 ° is 0.25 μm or less. The titanyl phthalocyanine crystal is at least 7.0 to 7.5 as a diffraction peak (± 0.2 °) with a Bragg angle 2θ with respect to the characteristic X-ray of CuKα (wavelength 1.542 mm). In the presence of water, amorphous titanyl phthalocyanine or low crystalline titanyl phthalocyanine having a maximum diffraction peak at 0 ° and a half-width of the diffraction peak of 1 ° or more and an average primary particle size of 0.1 μm or less in the presence of water The titanyl phthalocyanine after crystal conversion from an organic solvent before the average size of primary particles after crystal conversion grows larger than 0.3 μm. Fractionation, an image forming apparatus which is characterized in that which has been filtered.
Electric field strength (V / μm) = surface potential of unexposed portion of photoreceptor at development position (V) / photosensitive layer thickness (μm)

  (2) The titanyl phthalocyanine crystal is a titanyl phthalocyanine crystal having a peak intensity of 26.3 ° in a range of 0.1 to 5% with respect to a peak intensity of a maximum diffraction peak of 27.2 °. The image forming apparatus according to item (1).

(3) The image formation according to item (1) or ( 2) , wherein the charge transport layer contains a polycarbonate having at least a triarylamine structure in the main chain and / or side chain. apparatus.

(4) The image forming apparatus according to any one of (1) to (3), wherein a protective layer is provided on the charge transport layer.

(5) The image forming apparatus as described in (4) above, wherein the protective layer contains a metal oxide having a specific resistance of 10 ¹⁰ Ω · cm or more.

(6) said first (4) the protective layer is characterized by containing a polymeric charge transport material section or the image forming apparatus according to the item (5).

(7) The image forming apparatus according to any one of (4) to (6), wherein the binder resin of the protective layer has a crosslinked structure.

(8) The image forming apparatus as described in (7) above, wherein the structure of the binder resin having the crosslinked structure has a charge transport site.

(9) The image forming apparatus as described in any one of (1) to (8) above, wherein the electroconductive support surface of the electrophotographic photosensitive member is anodized. .

(10) Any one of (1) to (9) above, wherein a plurality of image forming elements comprising at least charging means, exposure means, developing means, transfer means, and electrophotographic photosensitive member are arranged. The image forming apparatus described in 1.

(11) The image forming apparatus according to any one of (1) to (10), wherein an AC superimposed voltage is applied to the charging unit.

(12) The apparatus main body in which the photosensitive member and at least one means selected from charging means, exposure means, developing means, and cleaning means are integrated, and a detachable cartridge are mounted . The image forming apparatus according to any one of items 1) to (11) .

According to the present invention, there is provided an image forming apparatus that outputs an image at a very high speed and that outputs a stable and high-resolution image without occurrence of an abnormal image when repeatedly used at a high speed. The
Specifically, in order to form a high-quality image, the photoconductor is charged so that an electric field strength of 30 V / μm or more is formed by a scorotron charging member, and writing is performed with a writing light source of 600 dpi or more. In an image forming apparatus for forming an electrostatic latent image, a titanyl phthalocyanine crystal having a specific crystal type and a specific particle size is used and operated at a photosensitive member linear velocity of 300 mm / sec or more. Provided is an image forming apparatus that maintains the high sensitivity inherent in phthalocyanine, is highly durable and capable of high-speed image output.

First, the image forming apparatus of the present invention will be described in detail with reference to the drawings.
FIG. 3 is a schematic diagram for explaining the image forming apparatus of the present invention, and the following modifications also belong to the category of the present invention.
In FIG. 3, the photosensitive member (1) is provided with a photosensitive layer including at least a charge generation layer and a charge transport layer on a conductive support, and the charge generation layer has a characteristic X-ray of CuKα (wavelength 1.542Å). As a diffraction peak (± 0.2 °) with a Bragg angle of 2θ, the maximum diffraction peak is at least 27.2 °, and the main peaks are at 9.4 °, 9.6 °, and 24.0 °. In addition, the diffraction peak on the lowest angle side has a peak at 7.3 °, and there is no peak between the peak at 7.3 ° and the peak at 9.4 °. It contains titanyl phthalocyanine crystals having an average particle size of primary particles having a peak at 3 ° of 0.25 μm or less. The photosensitive member (1) has a drum shape, but may be a sheet or an endless belt.

The photosensitive member linear velocity (system linear velocity) of the apparatus shown in FIG. 3 is operated at 300 mm / sec or more in correspondence with high-speed image output.
As the charging member (3), a scorotron charging member is preferably used for the photoreceptor. By this charging member, an electric field strength of 30 V / μm or more is applied to the photoreceptor. The higher the electric field strength applied to the photoconductor, the better the dot reproducibility. However, there is a possibility of causing problems of dielectric breakdown of the photoconductor and carrier adhesion at the time of development, and the upper limit is about 60 V / μm or less. Preferably, it is 50 V / μm or less.

  The transfer charger (10) may be a transfer belt or a transfer roller, but it is desirable to use a contact type such as a transfer belt or transfer roller that generates less ozone. As a voltage / current application method at the time of transfer, either a constant voltage method or a constant current method can be used, but the transfer charge amount can be kept constant, and a constant voltage with excellent stability can be used. The current method is more desirable.

  Of the charging methods, a scorotron charging method is desirable for at least a charging member (indicated as the charging charger (3) in FIG. 3) used for main charging to the photosensitive member.

  The image exposure unit (5) uses a light source capable of ensuring high brightness and capable of writing at a resolution of 600 dpi or more, such as a light emitting diode (LED), a semiconductor laser (LD), and electroluminescence (EL). . Depending on the resolution of the light source (writing light), the resolution of the formed electrostatic latent image, and thus the toner image, is determined. The higher the resolution, the clearer the image. However, if writing is performed at a higher resolution, writing takes longer, so writing with one writing light source is limited by the drum linear speed (process speed).

  Therefore, when there is one writing light source, a resolution of about 1200 dpi is the upper limit. When there are a plurality of write light sources, each of them only has to bear a write area, and the upper limit is substantially “1200 dpi × number of write light sources”. Among these light sources, light emitting diodes and semiconductor lasers have high irradiation energy and long wavelength light of 600 to 800 nm. Therefore, the specific crystal type phthalocyanine pigment which is a charge generation material used in the present invention has high sensitivity. Used well from showing.

  The developing unit (6) can handle both normal development and reversal development depending on the charging polarity of the toner used. When toner having a polarity opposite to the charged polarity of the photoreceptor is used, normal development is used. When toner having the same polarity is used, the electrostatic latent image is developed by reversal development. Depending on the light source used in the previous image exposure unit, in the case of a digital light source used in recent years, there is generally a reversal development method in which toner development is performed on the writing portion in response to a low image area ratio. This is advantageous in view of the life of the light source. There are two methods, a one-component method in which development is performed using only toner and a two-component method in which a two-component developer composed of toner and carrier is used.

Further, the toner image formed on the photosensitive member is transferred to the transfer paper and becomes an image on the transfer paper. At this time, there are two methods. One is a method of directly transferring a toner image developed on the surface of the photosensitive member as shown in FIG. 3 to the transfer paper, and the other is that the toner image is once transferred from the photosensitive member to the intermediate transfer member, and this is transferred to the transfer paper. It is the method of transferring to. Either case can be used in the present invention.
As the transfer member, a transfer belt can be used, but in addition, a transfer charger (10) and a transfer roller shown in FIG. 3 can also be used. Among them, it is desirable to use a contact type such as a transfer belt or a transfer roller that generates less ozone. As such a transfer member, a known member can be used as long as the structure of the present invention can be satisfied.

  Use light sources such as fluorescent lamps, tungsten lamps, halogen lamps, mercury lamps, sodium lamps, light-emitting diodes (LEDs), semiconductor lasers (LDs), and electroluminescence (ELs) as light sources such as static elimination lamps (2). Can do. Various types of filters such as a sharp cut filter, a band pass filter, a near infrared cut filter, a dichroic filter, an interference filter, and a color temperature conversion filter can be used to irradiate only light in a desired wavelength range.

Such a light source or the like irradiates the photosensitive member with light by providing a process such as a transfer process, a charge eliminating process, a cleaning process, or a pre-exposure using light irradiation in addition to the process shown in FIG.
This neutralization mechanism can be omitted when the AC component is superposed and used in the previous charging method, or when the residual potential of the photoreceptor is small. Further, instead of optical static elimination, an electrostatic static elimination mechanism (for example, a static elimination brush with a reverse bias applied or grounded) can be used.

  Further, the toner developed on the photosensitive member (1) by the developing unit (6) is transferred to the transfer paper (7). If toner remaining on the photosensitive member (1) is generated, a fur brush ( 14) and the blade (15) to remove from the photoreceptor. Cleaning may be performed only with a cleaning brush, and a known brush such as a fur brush or a mag fur brush is used as the cleaning brush.

FIG. 4 is a schematic diagram for explaining the tandem-type full-color image forming apparatus of the present invention, and the following modifications also belong to the category of the present invention.
In FIG. 4, reference numerals (16Y), (16M), (16C), and (16K) are drum-shaped photoconductors, and the photoconductor (1) has at least a charge generation layer and a charge transport layer on a conductive support. The charge generation layer has a maximum diffraction peak at least 27.2 ° as a Bragg angle 2θ diffraction peak (± 0.2 °) with respect to CuKα characteristic X-rays (wavelength 1.542 mm). And the main peaks at 9.4 °, 9.6 °, and 24.0 °, and the peak at 7.3 ° as the lowest diffraction peak, It has no peak between the peak at 3 ° and the peak at 9.4 °, and further contains titanyl phthalocyanine crystals having an average particle size of 0.25 μm or less of primary particles having a peak at 26.3 °. Become.

The photoconductors (16Y), (16M), (16C), and (16K) rotate at a speed of 300 mm / sec or more in the direction of the arrow in the drawing, and around them, at least in the order of rotation, a scorotron charging member (17Y), (17M), (17C), (17K), developing members (19Y), (19M), (19C), (19K), cleaning members (20Y), (20M), (20C), (20K) are arranged. ing. The charging members (17Y), (17M), (17C), and (17K) are charging members that constitute a charging device for uniformly charging the surface of the photoreceptor. From an exposure member (not shown) from the back side of the photoreceptor between the charging members (17Y), (17M), (17C), (17K) and the developing members (19Y), (19M), (19C), (19K). Laser beams (18Y), (18M), (18C), and (18K) are irradiated so that an electrostatic latent image is formed on the photoconductors (16Y), (16M), (16C), and (16K). It has become.
Then, the four image forming elements (25Y), (25M), (25C), and (25K) centering on such photoconductors (16Y), (16M), (16C), and (16K) serve as transfer materials. They are juxtaposed along the transfer conveyance belt (22) which is a conveyance means. The transfer / conveying belt (22) includes developing members (19Y), (19M), (19C), (19K) and cleaning members (20Y) of the image forming units (25Y), (25M), (25C), (25K). , (20M), (20C), and (20K) are in contact with the photosensitive member (16Y), (16M), (16C), and (16K), and contact the back side of the photosensitive member side of the transfer conveyance belt (22). Transfer brushes (21Y), (21M), (21C), and (21K) for applying a transfer bias are arranged on the surface (back surface). Each of the image forming elements (25Y), (25M), (25C), and (25K) 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. 4, the image forming operation is performed as follows. First, in each of the image forming elements (25Y), (25M), (25C), and (25K), an electrostatic latent image is formed on the photoconductors (16Y), (16M), (16C), and (16K). It has become. Then, such photoconductors (16Y), (16M), (16C), and (16K) rotate at a speed of 300 mm / sec or more, and scorotron charging members (17Y), (17M), (17C), By (17K), the photosensitive member is charged so that the electric field strength is 30 V / μm or more (60 V μm or less, preferably 50 V / μm or less).

  Next, writing is performed at a resolution of 600 dpi or more by laser light (18Y), (18M), (18C), and (18K) at an exposure unit (not shown) arranged inside the photoconductor, and each color to be created is written. An electrostatic latent image corresponding to the image is formed. Also in this case, 1200 dpi writing is generally the upper limit for one writing light source.

  Next, the latent image is developed by the developing members (19Y), (19M), (19C), and (19K) to form a toner image. Development members (19Y), (19M), (19C), and (19K) are development members that perform development with toners of Y (yellow), M (magenta), C (cyan), and K (black), respectively. The toner images of the respective colors formed on the two photoconductors (16Y), (16M), (16C), and (16K) are superimposed on the transfer paper.

  The transfer paper (26) is fed out from the tray by a paper feeding roller (not shown), temporarily stopped by a pair of registration rollers (23), and transferred and conveyed (22) in synchronization with the image formation on the photosensitive member. ). The transfer paper (26) held on the transfer conveyance belt (22) is conveyed, and each color is in contact with each photoconductor (16Y), (16M), (16C), (16K) (transfer section). The toner image is transferred. The toner image on the photoconductor includes transfer bias applied to the transfer brushes (21Y), (21M), (21C), and (21K) and the photoconductors (16Y), (16M), (16C), and (16K). The image is transferred onto the transfer paper (26) by an electric field formed from the potential difference.

  Then, the recording paper (26) on which the four color toner images are passed through the four transfer sections is conveyed to the fixing device (24), where the toner is fixed, and is discharged to a paper discharge section (not shown).

  Further, residual toner remaining on each of the photoconductors (16Y), (16M), (16C), and (16K) without being transferred by the transfer unit is removed from the cleaning devices (20Y), (20M), (20C), ( 20K).

  In the example of FIG. 4, the image forming elements are arranged in the order of Y (yellow), M (magenta), C (cyan), and K (black) from the upstream side to the downstream side in the transfer sheet conveyance direction. However, it is not limited to this order, and the color order is arbitrarily set. Further, when creating a black-only document, it is particularly effective to use the present invention to provide a mechanism that stops image forming elements other than black ((25Y), (25M), (25C)). .

  The image forming means as described above may be fixedly incorporated in a copying apparatus, facsimile, or printer, but each electrophotographic element may be incorporated in the apparatus in the form of a process cartridge. A process cartridge is a single device (part) that contains a photoconductor and further includes a charging unit, an exposure unit, a developing unit, a transfer unit, a cleaning unit, a neutralizing unit, and the like.

  The image forming means as described above may be fixedly incorporated in a copying apparatus, a facsimile, or a printer, but may be incorporated in these apparatuses in the form of a process cartridge. A process cartridge is a single device (part) that contains a photoconductor and further includes a charging unit, an exposure unit, a developing unit, a transfer unit, a cleaning unit, a neutralizing unit, and the like. There are many shapes and the like of the process cartridge, but a general example is shown in FIG. The photoreceptor (101) is provided with a photosensitive layer including at least a charge generation layer and a charge transport layer on a conductive support. The charge generation layer has a Bragg angle 2θ with respect to a characteristic X-ray of CuKα (wavelength 1.542Å). Diffraction peak (± 0.2 °) having a maximum diffraction peak at least 27.2 °, and further having major peaks at 9.4 °, 9.6 °, 24.0 °, and most The diffraction peak on the low angle side has a peak at 7.3 °, and there is no peak between the peak at 7.3 ° and the peak at 9.4 °, and a peak at 26.3 °. Primary particles having a mean particle size of 0.25 μm or less containing titanyl phthalocyanine crystals.

  As described above, a light source capable of writing with a resolution of 600 dpi or higher is used for the image exposure unit (103), and a scorotron charging member is used for the charging member (102) as described above. An electric field strength of 30 V / μm or more (60 V / μm or less, preferably 50 V / μm or less) is applied to the photoreceptor. In FIG. 5, 104 is a developing means, 105 is a transfer member, 106 is a transfer means, and 107 is a cleaning means.

The electrophotographic photoreceptor used in the image forming apparatus of the present invention will be described in detail below.
The electrophotographic photosensitive member used in the present invention is an electrophotographic photosensitive member in which at least a charge generation layer and a charge transport layer are formed on a conductive support, and a characteristic X-ray of CuKα ( As a diffraction peak (± 0.2 °) with a Bragg angle 2θ for a wavelength of 1.542 mm, it has a maximum diffraction peak of at least 27.2 °, and further at 9.4 °, 9.6 °, and 24.0 °. It has a main peak, and has a peak at 7.3 ° as the lowest diffraction peak, and has a peak between the 7.3 ° peak and the 9.4 ° peak. Furthermore, it contains a titanyl phthalocyanine crystal having an average particle size of primary particles having a peak at 26.3 ° and an average particle size of 0.25 μm or less.

This crystal type is described in JP-A No. 2001-187794. By using this titanyl phthalocyanine crystal, it is stable without causing a decrease in chargeability even after repeated use without losing high sensitivity. An electrophotographic photoreceptor can be obtained.
Japanese Patent Application Laid-Open No. 2001-187794 discloses a charge generating material used in the present invention, a photoreceptor using the same, an electrophotographic apparatus, and the like. However, in a situation where the resolution is 600 dpi or higher or 1200 dpi or higher, it is necessary to increase the intensity of the electric field applied to the photosensitive member in order to make use of the writing resolution. However, when the electric field strength is high, there is a problem that soiling occurs. Such a phenomenon remarkably appears when used in an image forming apparatus that performs writing with higher resolution than the image forming apparatus described in the publication. Thus, in the past process (apparatus), not only the ability of the material described in the same publication is not sufficiently drawn out, but if the process conditions are not optimized, a side effect is produced.
Japanese Patent Laid-Open No. 2001-19871 does not have a description of particle size and a technique for controlling the particle size, and the particle size has not been optimized. In the present invention, a more optimal image forming apparatus is constructed by using a photoconductor containing a specific crystal type titanyl phthalocyanine having a controlled particle size and optimizing the process conditions of the image forming apparatus.

  Further, as a method for synthesizing titanyl phthalocyanine crystals, a method using no titanium halide as a raw material can be favorably used as described in JP-A-6-293769. The biggest merit of this method is that the synthesized titanyl phthalocyanine crystal is free of halogenation. When a titanyl phthalocyanine crystal contains a halogenated titanyl phthalocyanine crystal as an impurity, it often has adverse effects such as a decrease in photosensitivity and a decrease in chargeability in the electrostatic characteristics of a photoconductor using the crystal (Japan Hardcopy '89 paper). Collection p.103 1989). Also in the present invention, the halogenated free titanyl phthalocyanine crystal as described in JP-A-2001-187794 is mainly used, and these materials are effectively used.

First, a method for synthesizing a titanyl phthalocyanine crystal having a specific crystal type used in the present invention will be described.
First, a method for synthesizing a crude product of titanyl phthalocyanine crystal will be described. Methods for synthesizing phthalocyanines have been known for a long time, and are described in “Phthalogyneines Compounds” (1963), “The Phthalogianines” (1983), and Japanese Patent Application Laid-Open No. Hei 6-293769 by Moser et al.

For example, as a first method, a mixture of phthalic anhydrides, metal or metal halide and urea is heated in the presence or absence of a high boiling point solvent. In this case, a catalyst such as ammonium molybdate is used in combination as necessary.
As a second method, phthalonitriles and metal halides are heated in the presence or absence of a high boiling point solvent. This method is used for phthalocyanines that cannot be produced by the first method, such as aluminum phthalocyanines, indium phthalocyanines, oxovanadium phthalocyanines, oxotitanium phthalocyanines, zirconium phthalocyanines, and the like.
The third method is to first react phthalic anhydride or phthalonitrile with ammonia to produce an intermediate such as 1,3-diiminoisoindoline, and then react with a metal halide in a high boiling solvent. It is a method to make it.
The fourth method is a method in which phthalonitriles and a metal alkoxide are reacted in the presence of urea or the like. In particular, the fourth method does not cause chlorination (halogenation) to the benzene ring, and is a very useful method as a method for synthesizing an electrophotographic material, and is used extremely effectively in the present invention.

  Next, a method for synthesizing amorphous titanyl phthalocyanine (low crystalline titanyl phthalocyanine) will be described. In this method, phthalocyanines are dissolved in sulfuric acid, diluted with water and reprecipitated, and an acid paste method or an acid slurry method can be used.

  As a specific method, the above synthetic crude product is dissolved in 10-50 times the amount of concentrated sulfuric acid, and if necessary, insoluble matter is removed by filtration or the like, and this is sufficiently cooled to 10-50 times the amount of sulfuric acid. Slowly throw it into water or ice water to reprecipitate titanyl phthalocyanine. The precipitated titanyl phthalocyanine is filtered, washed with ion-exchanged water and filtered, and this operation is sufficiently repeated until the filtrate becomes neutral. Finally, after washing with clean ion-exchanged water, filtration is performed to obtain a water paste having a solid content concentration of about 5 to 15 wt%. What was produced in this way was the amorphous titanyl phthalocyanine (low crystalline titanyl phthalocyanine) used in the present invention. In this case, the amorphous titanyl phthalocyanine (low crystalline titanyl phthalocyanine) is at least 7.0 to 7 as a diffraction peak (± 0.2 °) with a Bragg angle 2θ with respect to the characteristic X-ray (wavelength 1.542Å) of CuKα. It is preferable to have a maximum diffraction peak at 5 °. In particular, the half width of the diffraction peak is more preferably 1 ° or more. Further, the average particle size of the primary particles is preferably 0.1 μm or less.

Next, a crystal conversion method will be described. In the present invention, titanyl phthalocyanine crystals are synthesized from at least two crystal conversion steps.
First, the first crystal conversion method will be described. In the first crystal conversion, the amorphous titanyl phthalocyanine (low crystalline titanyl phthalocyanine) is used as a diffraction peak (± 0.2 °) of Bragg angle 2θ with respect to the characteristic X-ray of CuKα (wavelength 1.542 mm). It has a maximum diffraction peak at 2 °, a major peak at 9.4 °, 9.6 ° and 24.0 °, and a peak at 7.3 ° as the lowest diffraction peak. And a titanyl phthalocyanine crystal having no peak between the peak at 7.3 ° and the peak at 9.4 ° and having no peak at 26.3 °.

As a specific method, the crystalline form is obtained by mixing and stirring together with an organic solvent in the presence of water without drying the amorphous titanyl phthalocyanine (low crystalline titanyl phthalocyanine). .
In this case, any organic solvent can be used as long as the desired crystal form can be obtained, but tetrahydrofuran, toluene, methylene chloride, carbon disulfide, orthodichlorobenzene, 1,1, Good results are obtained when one selected from 2-trichloroethane is selected. These organic solvents are preferably used alone, but two or more of these organic solvents may be mixed or used in combination with other solvents. It is desirable that the amount of the organic solvent used for crystal conversion is 10 times or more, preferably 30 times or more the weight of amorphous titanyl phthalocyanine. This is because crystal conversion is caused quickly and sufficiently, and an effect of sufficiently removing impurities contained in amorphous titanyl phthalocyanine is exhibited.

  The amorphous titanyl phthalocyanine used here is prepared by the acid paste method, but it is desirable to use one obtained by sufficiently washing sulfuric acid as described above. When crystal conversion is performed under conditions where sulfuric acid remains, sulfate ions remain in the crystal particles, and the completed crystals cannot be completely removed even by an operation such as washing with water. When sulfate ions remain, preferable results cannot be obtained, such as a decrease in sensitivity and a decrease in chargeability of the photoreceptor. For example, JP-A-8-110649 (comparative example) describes a method of performing crystal conversion by adding titanyl phthalocyanine dissolved in sulfuric acid into an organic solvent together with ion-exchanged water. At this time, a crystal similar to the X-ray diffraction spectrum of the titanyl phthalocyanine crystal obtained in the present invention can be obtained, but the sulfate ion concentration in titanyl phthalocyanine is high and the light attenuation characteristic (photosensitivity) is poor. However, the method for producing titanyl phthalocyanine of the present invention is not good.

  The above crystal conversion method is a crystal conversion method according to Japanese Patent Laid-Open No. 2001-187794. On the other hand, in the charge generation material contained in the photoreceptor used in the electrophotographic apparatus of the present invention, the effect is achieved by making the particle size of the titanyl phthalocyanine crystal finer (0.25 μm or less). . The following describes a method for synthesizing titanyl phthalocyanine particle size smaller than the synthesis step.

In order to make the particle size of the titanyl phthalocyanine crystal finer, the present inventors have observed that the above-mentioned amorphous titanyl phthalocyanine (low crystalline titanyl phthalocyanine) has a primary particle size of 0.1 μm or less (its Although most of them are about 0.01 to 0.05 μm) (see FIG. 6), it has been found that the crystals are converted with crystal growth during the crystal conversion. Usually, in this type of crystal conversion, a sufficient crystal conversion time is ensured due to fear of remaining of the raw material, and after the crystal conversion is sufficiently performed, filtration is performed to obtain a titanyl phthalocyanine crystal having a desired crystal type. Is what you get. For this reason, even though a raw material having sufficiently small primary particles is used as a raw material, a crystal having a large primary particle (approximately 0.3 to 0.5 μm) is obtained as a crystal after crystal conversion. Yes (see FIG. 7).
The scale bars in the figure are all 0.2 μm.

  When dispersing the titanyl phthalocyanine crystal produced as shown in FIG. 7, in order to make the particle size after dispersion small (0.25 μm or less), dispersion is performed by giving a strong share, and further necessary. In response to this, dispersion is performed by giving strong energy to pulverize the primary particles. As a result, as described above, there is a possibility that a part of the particles may be transferred to a crystal type which is not a desired crystal type.

  In this regard, by controlling the primary particle size of the titanyl phthalocyanine crystal from the synthesis stage to obtain a crystal having a small size, a method for solving this problem is possible and it is effectively used in the present invention. Specifically, the range in which crystal growth hardly occurs during crystal conversion (the range in which the size of the amorphous titanyl phthalocyanine particles observed in FIG. 6 is insignificantly small after crystal conversion, approximately 0.25 μm or less. ) Is to obtain a titanyl phthalocyanine crystal having a primary particle size as small as possible by determining when the crystal conversion is completed. The particle size after crystal conversion increases in proportion to the crystal conversion time. For this reason, as described above, it is important to increase the efficiency of crystal conversion and complete it in a short time. There are several important points for this.

  One is to select an appropriate crystal conversion solvent as described above to increase the crystal conversion efficiency. The other is to use strong agitation to bring the solvent into contact with the titanyl phthalocyanine aqueous paste (raw material prepared as described above) in order to complete the crystal conversion in a short time. Specifically, it is possible to achieve crystal conversion in a short time by using a propeller with a very strong stirring force or using a strong stirring (dispersing) means such as a homogenizer (homomixer). is there. Under these conditions, it is possible to obtain a titanyl phthalocyanine crystal in a state in which crystal conversion is sufficiently performed and crystal growth does not occur without remaining raw materials.

  In addition, since the crystal grain size and the crystal conversion time are in a proportional relationship as described above, a method of immediately stopping the reaction when a predetermined reaction (crystal conversion) is completed is also an effective means. As the above-mentioned means, it is possible to immediately add a large amount of a solvent in which crystal conversion hardly occurs after crystal conversion as described above. Examples of the solvent that hardly causes crystal transformation include alcohol-based and ester-based solvents. Crystal conversion can be stopped by adding about 10 times these solvents to the crystal conversion solvent.

  The smaller the primary particle size produced in this way, the better the results for the problem of the photoreceptor, but the next step for pigment preparation (pigment filtration step), dispersion in dispersion In consideration of stability, side effects may occur even if it is too small. That is, when the primary particles are very fine, there arises a problem that the filtration time becomes very long in the step of filtering the primary particles. In addition, when the primary particles are too fine, the surface area of the pigment particles in the dispersion increases, and the possibility of reaggregation of the particles increases. Therefore, the suitable particle size of the pigment particles is in the range of about 0.05 μm to 0.2 μm.

  FIG. 8 shows a TEM image of a titanyl phthalocyanine crystal when crystal conversion is performed in a short time. The scale bar in the figure is 0.2 μm. Unlike the case of FIG. 7, the particle size is small and almost uniform, and the coarse particles observed in FIG. 7 are not recognized at all.

  As shown in FIG. 8, when dispersing the titanyl phthalocyanine crystal produced in a state where the primary particles are small, the particle size after dispersion is made small (0.25 μm or less, more preferably 0.2 μm or less). For this purpose, it is possible to disperse by giving a share sufficient to loosen the secondary particles formed by aggregation of the primary particles. As a result, since the energy more than necessary is not given, a dispersion liquid with a fine particle size distribution can be easily produced without producing the result that a part of the particles are easily transferred to a crystal form other than the desired crystal form as described above. It is possible.

  The particle size referred to here is a volume average particle size and is determined by an ultracentrifugal automatic particle size distribution analyzer: CAPA-700 (manufactured by Horiba, Ltd.). At this time, the particle size (Median system) corresponding to 50% of the cumulative distribution was calculated. However, this method may not be able to detect a very small amount of coarse particles. Therefore, in order to obtain more details, it is important to observe the titanyl phthalocyanine crystal powder or dispersion directly with an electron microscope and determine its size. It is.

  As a result of further observation of the dispersion and examination of micro defects, the above phenomenon was understood as follows. Usually, in the method of measuring the average particle size, when an extremely large particle is present in several% or more, the presence can be detected, but it is about 1% or less of the whole. When the amount is too small, the measurement is below the detection limit. As a result, the presence of coarse particles is not detected only by measuring the average particle size, making it difficult to interpret the above minute defects.

  FIG. 9 and FIG. 10 show photographs observing the states of two types of dispersions in which only the dispersion time is changed while fixing the dispersion conditions. A photograph of a dispersion liquid having a short dispersion time under the same conditions is shown in FIG. 9, and it is observed that coarse particles remain as compared with FIG. 10 having a long dispersion time. The black particles in FIG. 9 are coarse particles.

The average particle size and particle size distribution of these two types of dispersions were measured by a commercially available particle size distribution measuring device (manufactured by Horiba: Ultracentrifugal automatic particle size distribution measuring device, CAPA700). The result is shown in FIG. “A” in FIG. 11 corresponds to the dispersion shown in FIG. 9, and “B” corresponds to the dispersion shown in FIG. When both are compared, there is almost no difference in the particle size distribution. In addition, the average particle diameter values of the two are “A” of 0.29 μm and “B” of 0.28 μm, and taking into account measurement errors, no difference is recognized between the two.
Therefore, it is understood that the remaining of a very small amount of coarse particles cannot be detected only by the definition of the known average particle size (particle size), and it is not possible to cope with the recent high-resolution negative / positive development. The presence of such a minute amount of coarse particles can be recognized for the first time by observing the coating solution at the microscope level.

  In response to such a fact, it is an effective means to produce as small primary particles as possible during the first crystal conversion. For this purpose, in order to complete the crystal conversion in a short time while selecting the appropriate crystal conversion solvent as described above and improving the crystal conversion efficiency, the solvent and titanyl phthalocyanine water paste (the raw material prepared as described above) are used. It can be seen that a technique using strong agitation is effective to sufficiently bring a contact of

  By adopting such a crystal conversion method, a titanyl phthalocyanine crystal having a small primary particle size (0.25 μm or less, more preferably 0.2 μm or less) can be obtained. In addition to the technique described in Japanese Patent Application Laid-Open No. 2001-187794, it is important in the present invention to use the above-described technique (crystal conversion method for obtaining fine titanyl phthalocyanine crystals) as necessary. Means.

Subsequently, the crystallized titanyl phthalocyanine crystal is immediately filtered to be separated from the crystal conversion solvent. This filtration is performed by using a filter of an appropriate size. In this case, it is most appropriate to use vacuum filtration.
Thereafter, the separated titanyl phthalocyanine crystal is heat-dried as necessary. Any known dryer can be used for heating and drying, but a blower-type dryer is preferable when the drying is performed in the atmosphere. Furthermore, drying under reduced pressure is also a very effective means in order to increase the drying speed and to exhibit the effects of the present invention more remarkably. In particular, this is an effective means for a material that decomposes at a high temperature or changes its crystal form. It is particularly effective to dry in a state where the degree of vacuum is higher than 10 mmHg.

The thus obtained titanyl phthalocyanine crystal having a specific crystal type is extremely useful as a charge generating material for an electrophotographic photoreceptor. However, as described above, the crystal form is unstable, and the crystal form is easily transferred when a dispersion is prepared. However, by synthesizing primary particles into infinitely small particles as in the present invention, a dispersion with a small average particle diameter can be prepared without giving an excessive share during the preparation of the dispersion, and the crystal type is also extremely high. It can be produced stably (without changing the synthesized crystal form).
Next, the second crystal conversion method will be described. The second crystal conversion is a step of further crystal conversion using the titanyl phthalocyanine crystal (dry powder) prepared by the first crystal conversion. Specific methods include two methods.

One is a method of treating the previously prepared titanyl phthalocyanine crystal in an organic solvent. As the organic solvent used, any solvent can be used as long as it can convert the crystal form having the maximum diffraction peak at 27.2 ° to the crystal form having the maximum diffraction peak at 26.3 °. Aromatic hydrocarbons such as xylene, ketones such as acetone and 2-butanone, halogenated hydrocarbons such as methylene chloride and chloroform, and cyclic ethers such as tetrahydrofuran are preferably used.
Regarding the treatment of the organic solvent, the titanyl phthalocyanine crystal may be simply immersed in the organic solvent as it is, but the treatment time can be shortened by using auxiliary means such as stirring and ultrasonic application together. ,It is valid. After the treatment with an organic solvent, the target titanyl phthalocyanine crystal can be obtained by separating by filtration and drying again.

  As another method, a crystal transformation is performed by applying a mechanical shearing force to the previously prepared titanyl phthalocyanine crystal. At this time, an organic solvent may be used in combination, but it is desirable to perform the treatment in a dry state without using it together. As a method to be used, dry milling using a ball mill, attritor, vibration mill, kneader, or the like, or simply dry milling using a mixer is also effective. Moreover, you may use inorganic salts, such as salt, as an adjuvant in the case of dry milling. When an auxiliary agent is used, a washing step for removing inorganic salts is necessary after the crystal conversion treatment. Thus, the target titanyl phthalocyanine crystal can be obtained.

Whichever method is used, it is important that the peak intensity at 26.3 ° is in the range of 0.1 to 5% with respect to the peak intensity at the maximum diffraction peak of 27.2 °. The peak intensity of 26.3 ° is determined by the treatment time in the solvent or the treatment time giving mechanical shearing force, but the state of the raw material used (the titanyl phthalocyanine crystal produced by the first crystal conversion) (for example, It is desirable to determine the treatment time through preliminary experiments because it varies depending on the size and hardness of the powder.
Next, a method for preparing the dispersion will be described.
A general method is used for the preparation of the dispersion, and the titanyl phthalocyanine crystal is dispersed in a suitable solvent together with a binder resin as necessary by using a ball mill, an attritor, a sand mill, a bead mill, an ultrasonic wave, or the like. It is obtained. At this time, the binder resin may be selected depending on the electrostatic characteristics of the photoreceptor, and the solvent may be selected depending on the wettability to the pigment, the dispersibility of the pigment, and the like.

  As already described, the titanyl phthalocyanine crystal having a maximum diffraction peak at 27.2 ° as a diffraction peak (± 0.2 °) with a Bragg angle 2θ with respect to the characteristic X-ray (wavelength 1.542 波長) of CuKα is It is known that crystal transition to other crystal forms easily occurs due to stress such as energy and mechanical share. This tendency does not change in the titanyl phthalocyanine crystal used in the present invention. In other words, in order to produce a dispersion containing fine particles, it is necessary to devise a dispersion method, but the stability of the crystal form and the micronization tend to be in a trade-off relationship. Although there are methods for avoiding this by optimizing the dispersion conditions, all of them make the manufacturing conditions extremely narrow, and a simpler method is desired. In order to solve this problem, the following method is also an effective means.

That is, it is a method in which a dispersion liquid in which the particles are made as fine as possible is produced within a range where crystal transition does not occur, and then filtered through an appropriate filter. This method is a very effective means in that it can remove a minute amount of coarse particles that cannot be visually observed (or cannot be detected by particle size measurement), and that the particle size distribution is uniform. Specifically, the dispersion prepared as described above is filtered through a filter having an effective pore size of 3 μm or less, more preferably 1 μm or less, thereby completing the dispersion.
Also by this method, a dispersion containing only titanyl phthalocyanine crystals having a small particle size (0.25 μm or less, more preferably 0.2 μm or less) can be produced, and a photoconductor using the dispersion is mounted on an image forming apparatus. By using it, the effect of the present application is made more remarkable.

  The filter for filtering the dispersion varies depending on the size of coarse particles to be removed, but according to the study by the present inventors, as a photoreceptor used in an electrophotographic apparatus that requires a resolution of about 600 dpi. The presence of coarse particles of at least 3 μm affects the image. Therefore, a filter with an effective pore size of 3 μm or less should be used. More preferably, a filter having an effective pore size of 1 μm or less is used. By performing such a filtering process, coarse particles finer than the effective pore size can be removed, and a dispersion having a narrow particle size distribution and no coarse particles can be produced.

  As for the effective pore size, the finer the particle, the more effective the removal of coarse particles. However, if the particle size is too fine, the necessary pigment particles themselves are also filtered, and therefore there is an appropriate size. In addition, if it is too fine, it takes time for filtration, clogging of the filter, and excessive load is applied when liquid is sent using a pump or the like. As a matter of course, a material having resistance to the solvent used in the dispersion to be filtered is used as the material of the filter used here.

  During filtration, if the amount of coarse particles in the dispersion to be filtered is too large, the amount of pigment to be removed increases, and the solid content concentration of the dispersion after filtration changes, which is not preferable. Therefore, an appropriate particle size distribution (particle size, standard deviation) exists when performing filtration. As in the present invention, there is no loss of pigment due to filtration, filter clogging, etc., and in order to perform filtration efficiently, the volume average particle size of the dispersion before filtration is 0.3 μm or less, and its standard deviation is It is desirable to disperse to 0.2 μm or less.

  By adding such an operation of filtering the dispersion, coarse particles can be removed, and as a result, background contamination generated on the photoconductor using the dispersion can be reduced. As described above, the finer the filter, the greater the effect (reliable), but there are cases where the pigment particles themselves are filtered. In such a case, using the titanyl phthalocyanine primary particles described above in combination with the technique for refining and synthesizing the particles produces a very large effect.

  That is, (i) by synthesizing and using refined titanyl phthalocyanine, the dispersion time can be shortened and the dispersion stress can be reduced, and the possibility of crystal transition in dispersion is reduced. (Ii) Since the size of the coarse particles remaining after dispersion is smaller than that in the case where the particles are not refined, a smaller filter can be used, and the effect of removing the coarse particles becomes more reliable. In addition, the amount of titanyl phthalocyanine particles to be removed is reduced, and there is little change in the composition of the dispersion before and after filtration, which enables stable production. (Iii) As a result, the manufactured photoreceptor is stably manufactured with high resistance to soiling.

The intensity ratio of the 26.3 ° peak intensity to the 27.2 ° peak intensity in the titanyl phthalocyanine crystal of the present invention will be described.
An X-ray diffraction spectrum is measured with a general X-ray diffractometer in a powder state of the titanyl phthalocyanine crystal to be used. Baseline correction is performed on the obtained spectrum, and then a peak intensity of 26.3 ± 0.2 ° and a peak intensity of 27.2 ± 0.2 ° are obtained. Using the value, the value obtained by dividing the peak intensity of 26.3 ± 0.2 ° by the peak intensity of 27.2 ± 0.2 ° is the peak intensity ratio in the present invention.
Peak intensity ratio (%) = 26.3 ± 0.2 ° peak intensity / 27.2 ± 0.2 ° peak intensity × 100
When the peak intensity ratio is 1% or less, it may be difficult to correct the baseline in measurement over a wide range. In that case, the intensity ratio can be obtained more accurately by narrowing the measurement range (for example, measuring within a range of 25 to 30 °) and performing remeasurement.

Next, the electrophotographic photosensitive member used in the present invention will be described in detail with reference to the drawings.
FIG. 12 is a cross-sectional view showing a structural example of the electrophotographic photosensitive member used in the present invention. On the conductive support (31), a titanyl phthalocyanine crystal having a specific crystal type with the specific particle size (charge generating material). ) As a main component and a charge transport layer (37) whose main component is a charge transport material are stacked.
FIG. 13 is a cross-sectional view showing another structural example of the electrophotographic photosensitive member used in the present invention, and a titanyl phthalocyanine crystal having the specific particle size and the specific particle size on the conductive support (31). A charge generation layer (35) mainly composed of (charge generation material) and a charge transport layer (37) mainly composed of a charge transport material are laminated, and a protective layer (39) is further formed on the charge transport layer. It has a configuration that is provided.

As the conductive support (31), a material having a volume resistance of 10 ¹⁰ Ω · cm or less, for example, a metal such as aluminum, nickel, chromium, nichrome, copper, gold, silver, platinum, tin oxide, oxidation Metal oxide such as indium by vapor deposition or sputtering, film or cylindrical plastic, paper coated, or aluminum, aluminum alloy, nickel, stainless steel plates, etc. and methods such as extrusion and drawing After forming the tube, it is possible to use a tube subjected to surface treatment such as cutting, superfinishing or polishing. Further, an endless nickel belt and an endless stainless steel belt disclosed in Japanese Patent Application Laid-Open No. 52-36016 can be used as the conductive support (31).

  Of these, a cylindrical support made of aluminum, which can be easily subjected to the anodic oxide film treatment, can be most preferably used. As used herein, aluminum includes both pure aluminum and aluminum alloys. Specifically, JIS 1000, 3000, and 6000 series aluminum or aluminum alloy is most suitable.

  Anodized films are obtained by anodizing various metals and various alloys in an electrolyte solution. Among them, a film called anodized aluminum or an aluminum alloy that has been anodized in an electrolyte solution is used in the present invention. Is the most suitable. In particular, it is excellent in preventing point defects (black spots, background stains) that occur when used in reversal development (negative / positive development).

The anodizing treatment is performed in an acidic bath such as chromic acid, sulfuric acid, oxalic acid, phosphoric acid, boric acid, sulfamic acid. Of these, treatment with a sulfuric acid bath is most suitable. For example, sulfuric acid concentration: 10 to 20%, bath temperature: 5 to 25 ° C., current density: 1 to 4 A / dm ² , electrolytic voltage: 5 to 30 V, treatment time: treatment in the range of about 5 to 60 minutes However, the present invention is not limited to this.

  Since the anodic oxide film produced in this way is porous and has high insulation, the surface is very unstable. For this reason, there is a change with time after fabrication, and the physical property value of the anodized film is likely to change. In order to avoid this, it is desirable to further seal the anodized film.

  Examples of the sealing treatment include a method of immersing the anodized film in an aqueous solution containing nickel fluoride and nickel acetate, a method of immersing the anodized film in boiling water, and a method of treating with pressurized steam. Among these, the method of immersing in the aqueous solution containing nickel acetate is the most preferable.

  Subsequent to the sealing treatment, the anodic oxide film is washed. The main purpose of this is to remove excess metal salts and the like attached by the sealing treatment. If this remains excessively on the surface of the support (anodized film), it not only adversely affects the quality of the coating film formed on this surface, but also generally low resistance components remain, resulting in the occurrence of soiling. It can also be a cause. The cleaning may be performed once with pure water, but is usually performed at another stage. At this time, it is preferable that the final cleaning liquid is as clean (deionized) as possible. Moreover, it is desirable to perform physical rubbing cleaning with a contact member in one of the other cleaning processes.

  The film thickness of the anodized film formed as described above is preferably about 5 to 15 μm. If it is too thin, the barrier effect as an anodic oxide film is not sufficient, and if it is too thick, the time constant as an electrode becomes too large, resulting in the generation of residual potential and the response of the photoreceptor. There is a case.

In addition to the above, a conductive powder dispersed in a suitable binder resin and coated on the support can be used as the conductive support (31) of the present invention.
Examples of the conductive powder include carbon black, acetylene black, metal powder such as aluminum, nickel, iron, nichrome, copper, zinc, and silver, or metal oxide powder such as conductive tin oxide and ITO. It is done.
The binder resin used at the same time is 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-vinylcarbazole, acrylic resin, silicone resin, epoxy resin, Examples thereof include thermoplastic, thermosetting resins, and photocurable resins such as melamine resin, urethane resin, phenol resin, and alkyd resin.
Such a conductive layer can be provided by dispersing and coating these conductive powder and binder resin in a suitable solvent such as tetrahydrofuran, dichloromethane, methyl ethyl ketone, and toluene.

  Furthermore, a heat-shrinkable tube in which the conductive powder is contained in a material such as polyvinyl chloride, polypropylene, polyester, polystyrene, polyvinylidene chloride, polyethylene, chlorinated rubber, polytetrafluoroethylene fluororesin on a suitable cylindrical substrate. Those provided with a conductive layer can be used favorably as the conductive support (31) of the present invention.

  Next, the photosensitive layer will be described. As described above, as the photosensitive layer, a laminated type composed of the charge generation layer (35) and the charge transport layer (37) exhibits excellent characteristics in sensitivity and durability, and is used favorably.

The charge generation layer (35) has, as a charge generation material, a maximum diffraction peak at 27.2 ° as a diffraction peak (± 0.2 °) with a Bragg angle 2θ with respect to CuKα characteristic X-rays (wavelength 1.542 mm). The crystal form). In particular, among the crystal types, there are further main peaks at 9.4 °, 9.6 °, 24.0 °, and the lowest diffraction angle has a peak at 7.3 °, In addition, there is no peak between the peak at 7.3 ° and the peak at 9.4 °, and the average particle size of primary particles having a peak at 26.3 ° is not more than 0.25 μm (preferably 0 .2 μm or less) titanyl phthalocyanine crystals are used favorably.
In the charge generation layer (35), the pigment is dispersed in a suitable solvent together with a binder resin, if necessary, using a ball mill, an attritor, a sand mill, an ultrasonic wave, or the like, and this is applied onto a conductive support. It is formed by drying.

As the binder resin used for the charge generation layer (35) as necessary, the binder resin used for the charge generation layer (35) as needed may be polyamide, polyurethane, epoxy resin, polyketone, polycarbonate, silicon. Resin, acrylic resin, polyvinyl butyral, polyvinyl formal, polyvinyl ketone, polystyrene, polysulfone, poly-N-vinylcarbazole, polyacrylamide, polyvinyl benzal, polyester, phenoxy resin, vinyl chloride-vinyl acetate copolymer, polyvinyl acetate, Polyphenylene oxide, polyamide, polyvinyl pyridine, cellulosic resin, casein, polyvinyl alcohol, polyvinyl pyrrolidone and the like can be mentioned.
The amount of the binder resin is suitably 0 to 500 parts by weight, preferably 10 to 300 parts by weight with respect to 100 parts by weight of the charge generating material.

  Examples of the solvent used here include isopropanol, acetone, methyl ethyl ketone, cyclohexanone, tetrahydrofuran, dioxane, ethyl cellosolve, ethyl acetate, methyl acetate, dichloromethane, dichloroethane, monochlorobenzene, cyclohexane, toluene, xylene, ligroin and the like. As a coating method for the coating solution, a dip coating method, spray coating, beat coating, nozzle coating, spinner coating, ring coating, or the like can be used.

  The thickness of the charge generation layer 35 is suitably about 0.01 to 5 μm, preferably 0.1 to 2 μm.

  The charge transport layer (37) can be formed by dissolving or dispersing a charge transport material and a binder resin in a suitable solvent, and applying and drying the solution on the charge generation layer. Moreover, a plasticizer, a leveling agent, antioxidant, etc. can also be added as needed.

  Charge transport materials include hole transport materials and electron transport materials.

  Examples of the electron transport 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 benzoquinone derivatives.

  Examples of the hole transport material include poly-N-vinylcarbazole and derivatives thereof, poly-γ-carbazolylethyl glutamate and derivatives thereof, pyrene-formaldehyde condensates and derivatives thereof, polyvinylpyrene, polyvinylphenanthrene, polysilane, oxazole derivatives, Oxadiazole derivatives, imidazole derivatives, monoarylamine derivatives, diarylamine derivatives, triarylamine derivatives, stilbene derivatives, α-phenylstilbene derivatives, benzidine derivatives, diarylmethane derivatives, triarylmethane derivatives, 9-styrylanthracene derivatives, pyrazolines Derivatives, divinylbenzene derivatives, hydrazone derivatives, indene derivatives, butadiene derivatives, pyrene derivatives, etc., bisstilbene derivatives, enamine derivatives, etc. Other known materials may be mentioned. These charge transport materials may be used alone or in combination of two or more.

Binder resins include polystyrene, styrene-acrylonitrile copolymer, styrene-butadiene copolymer, styrene-maleic anhydride copolymer, polyester, polyvinyl chloride, vinyl chloride-vinyl acetate copolymer, polyvinyl acetate, poly Vinylidene chloride, polyarate, phenoxy resin, polycarbonate, cellulose acetate resin, ethyl cellulose resin, polyvinyl butyral, polyvinyl formal, polyvinyl toluene, poly-N-vinylcarbazole, acrylic resin, silicone resin, epoxy resin, melamine resin, urethane resin, phenol resin And thermoplastic or thermosetting resins such as 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. The thickness of the charge transport layer is preferably about 5 to 100 μm.

  As the solvent used here, tetrahydrofuran, dioxane, toluene, dichloromethane, monochlorobenzene, dichloroethane, cyclohexanone, methyl ethyl ketone, acetone and the like are used. Among them, the use of a non-halogen solvent is desirable for the purpose of reducing the environmental load. Specifically, cyclic ethers such as tetrahydrofuran, dioxolane and dioxane, aromatic hydrocarbons such as toluene and xylene, and derivatives thereof are preferably used.

  In addition, a polymer charge transport material having a function as a charge transport material and a function of a binder resin is also preferably used for the charge transport layer. The charge transport layer composed of these polymer charge transport materials is excellent in wear resistance. As the polymer charge transport material, known materials can be used, and in particular, a polycarbonate containing a triarylamine structure in the main chain and / or side chain is preferably used. Among these, polymer charge transport materials represented by the formulas (I) to (X) are preferably used, and these are exemplified below and specific examples are shown.

In the formula, R1, R2, and R3 are each independently an optionally substituted alkyl group or a halogen atom, R4 is a hydrogen atom or an optionally substituted alkyl group, and R5 and R6 are optionally substituted aryl. Group, o, p and q are each independently an integer of 0 to 4, k and j are compositions, 0.1 ≦ k ≦ 1, 0 ≦ j ≦ 0.9, and n is the number of repeating units. It is an integer of ˜5000. X represents an aliphatic divalent group, a cycloaliphatic divalent group, or a divalent group represented by the following general formula. In the formula (I), two copolymer species are described in the form of an alternating copolymer, but a random copolymer may be used.

R101 and R102 each independently represents an optionally substituted alkyl group, aryl group or halogen atom. l and m are integers of 0 to 4, Y is a single bond, a linear, branched or cyclic alkylene group having 1 to 12 carbon atoms, —O—, —S—, —SO—, —SO ₂ —. , -CO-, -CO-O-Z-O-CO- (wherein Z represents an aliphatic divalent group) or

(A represents an integer of 1 to 20, b represents an integer of 1 to 2000, and R103 and R104 each represents an optionally substituted alkyl group or aryl group). Here, R101 and R102, and R103 and R104 may be the same or different. )

In the formula, R7 and R8 each represents an optionally substituted aryl group, and Ar1, Ar2, and Ar3 each represent the same or different arylene group. X, k, j and n are the same as in the case of formula (I). In the formula (II), two copolymer species are described in the form of an alternating copolymer, but a random copolymer may be used.

In the formula, R9 and R10 each represents an optionally substituted aryl group, and Ar4, Ar5 and Ar6 each represent the same or different arylene group. X, k, j and n are the same as in the case of formula (I). In the formula (III), two copolymer species are described in the form of an alternating copolymer, but a random copolymer may be used.

In the formula, R11 and R12 are optionally substituted aryl groups, Ar7, Ar8 and Ar9 are the same or different arylene groups, and p represents an integer of 1 to 5. X, k, j and n are the same as in the case of formula (I). In the formula (IV), two copolymer species are described in the form of an alternating copolymer, but a random copolymer may be used.

In the formula, R13 and R14 are aryl groups which may be substituted, Ar10, Ar11 and Ar12 are the same or different arylene groups, X1, X2 Represents an optionally substituted ethylene group or an optionally substituted vinylene group. X, k, j and n are the same as in the case of formula (I). In the formula (V), two copolymer species are described in the form of an alternating copolymer, but a random copolymer may be used.

In the formula, R15, R16, R17, and R18 are aryl groups that may be substituted, Ar13, Ar14, Ar15, and Ar16 are the same or different arylene groups, Y1, Y2, and Y3 are single bonds and alkylenes that may be substituted Represents a group, an optionally substituted cycloalkylene group, an optionally substituted alkylene ether group, an oxygen atom, a sulfur atom, or a vinylene group, which may be the same or different. X, k, j, and n are the same as in the formula (VI). In the formula (I), two copolymer species are described in the form of an alternating copolymer, but a random copolymer may be used.

In the formula, R19, R20 Represents a hydrogen atom or an optionally substituted aryl group, and R19 and R20 may form a ring. Ar17, Ar18, Ar19 Represent the same or different arylene groups. X, k, j and n are the same as in the case of formula (I). In the formula (VII), two copolymer species are described in the form of an alternating copolymer, but a random copolymer may be used.

In the formula, R21 is an optionally substituted aryl group, Ar20, Ar21, Ar22, Ar23. Represent the same or different arylene groups. X, k, j and n are the same as in the case of formula (I). In the formula (VIII), two copolymer species are described in the form of an alternating copolymer, but a random copolymer may be used.

In the formula, R22, R23, R24, and R25 each represents an optionally substituted aryl group, and Ar24, Ar25, Ar26, Ar27, and Ar28 represent the same or different arylene groups. X, k, j and n are the same as in the case of formula (I). In the formula (IX), two copolymer species are described in the form of an alternating copolymer, but a random copolymer may be used.

In the formula, R26 and R27 each represents an optionally substituted aryl group, and Ar29, Ar30, and Ar31 each represent the same or different arylene group. X, k, j and n are the same as in the case of formula (I). In the formula (X), two copolymer species are described in the form of an alternating copolymer, but a random copolymer may be used.

  Further, as the polymer charge transport material used in the charge transport layer, in addition to the polymer charge transport material described above, in the state of the monomer or oligomer having an electron donating group at the time of film formation of the charge transport layer, A polymer having a two-dimensional or three-dimensional crosslinked structure is finally included by carrying out a curing reaction or a crosslinking reaction.

  A charge transport layer composed of a polymer having these electron donating groups or a polymer having a crosslinked structure is excellent in wear resistance. Usually, in the electrophotographic process, since the charging potential (unexposed portion potential) is constant, if the surface layer of the photoreceptor is worn by repeated use, the electric field strength applied to the photoreceptor increases accordingly. As the electric field strength increases, the occurrence frequency of scumming increases. Therefore, the high wear resistance of the photosensitive member is advantageous for scumming. The charge transport layer composed of a polymer having these electron donating groups is a polymer compound, so it has excellent film-forming properties and has a charge transport site compared to a charge transport layer composed of a low molecular weight dispersed polymer. It can be configured with high density and has excellent charge transport capability. For this reason, a photoreceptor having a charge transport layer using a polymer charge transport material can be expected to have a high response speed.

  Examples of other polymers having an electron donating group include copolymers of known monomers, block polymers, graft polymers, star polymers, and, for example, JP-A-3-109406, JP-A-2000- It is also possible to use a cross-linked polymer having an electron donating group as disclosed in JP-A-206723 and JP-A No. 2001-34001.

In the present invention, a plasticizer or a leveling agent may be added to the charge transport layer (37).
As the plasticizer, those used as general plasticizers such as dibutyl phthalate and dioctyl phthalate can be used as they are, and the amount used is suitably about 0 to 30% by weight based on the binder resin.
As the leveling agent, silicone oils such as dimethyl silicone oil and methylphenyl silicone oil, polymers or oligomers having a perfluoroalkyl group in the side chain are used, and the amount used is 0 to 0 with respect to the binder resin. 1% by weight is suitable.

In the electrophotographic photoreceptor of the present invention, an intermediate layer can be provided between the conductive support (31) and the photosensitive layer.
In general, the intermediate layer is mainly composed of a resin. However, considering that the photosensitive layer is coated with a solvent on these resins, it is desirable that the resin be a resin having high solvent resistance with respect to a general organic solvent. . Examples of such resins include water-soluble resins such as polyvinyl alcohol, casein, and sodium polyacrylate, alcohol-soluble resins such as copolymer nylon and methoxymethylated nylon, polyurethane, melamine resin, phenol resin, alkyd-melamine resin, and epoxy. Examples thereof include a curable resin that forms a three-dimensional network structure such as a resin. Further, fine powder pigments of metal oxides exemplified by titanium oxide, silica, alumina, zirconium oxide, tin oxide, indium oxide and the like may be added to the intermediate layer in order to prevent moire and reduce residual potential.

These intermediate layers can be formed by using an appropriate solvent and coating method like the above-mentioned photosensitive layer. Furthermore, a silane coupling agent, a titanium coupling agent, a chromium coupling agent, or the like can be used as the intermediate layer of the present invention. In addition, in the intermediate layer of the present invention, Al ₂ O ₃ is provided by anodic oxidation, organic substances such as polyparaxylylene (parylene), SiO ₂ , SnO ₂ , TiO ₂ , ITO, CeO _2, etc. Those provided with an inorganic material by a vacuum thin film forming method can also be used favorably. In addition, known ones can be used. The thickness of the intermediate layer is suitably from 0 to 5 μm.

  In the electrophotographic photoreceptor of the present invention, a protective layer may be provided on the photosensitive layer for the purpose of protecting the photosensitive layer. In recent years, computers have been used on a daily basis, and there has been a demand for miniaturization of devices as well as high-speed output by printers. Therefore, by providing a protective layer and improving the durability, the photosensitive member of the present invention having high sensitivity and no abnormal defects can be used effectively.

  Materials used for the protective layer (39) include ABS resin, ACS resin, olefin-vinyl monomer copolymer, chlorinated polyether, allyl resin, phenol resin, polyacetal, polyamide, polyamideimide, polyacrylate, polyallylsulfone. , Polybutylene, polybutylene terephthalate, polycarbonate, polyarylate, polyethersulfone, polyethylene, polyethylene terephthalate, polyimide, acrylic resin, polymethylbenten, polypropylene, polyphenylene oxide, polysulfone, polystyrene, AS resin, butadiene-styrene copolymer, polyurethane , Resins such as polyvinyl chloride, polyvinylidene chloride, and epoxy resin. Of these, polycarbonate or polyarylate can be most preferably used.

In addition to the protective layer, fluorine resins such as polytetrafluoroethylene, silicone resins, and inorganic fillers such as titanium oxide, tin oxide, potassium titanate, and silica for the purpose of improving wear resistance (inorganic pigments) ), Or an organic filler (organic pigment) dispersed therein can be added.
Among the filler materials used for the protective layer of the photoreceptor, examples of the organic filler material include fluorine resin powder such as polytetrafluoroethylene, silicone resin powder, a-carbon powder, and the like. Metals such as copper, tin, aluminum and indium, silica, tin oxide, zinc oxide, titanium oxide, indium oxide, antimony oxide, bismuth oxide, tin oxide doped with antimony, tin doped indium oxide and other metals Examples thereof include inorganic materials such as oxides and potassium titanate. In particular, it is advantageous to use an inorganic material among them from the viewpoint of the hardness of the filler. In particular, silica, titanium oxide, and alumina can be used effectively.

The filler concentration in the protective layer varies depending on the type of filler used and also on the electrophotographic process conditions using the photoconductor, but the ratio of filler to the total solid content on the outermost layer side of the protective layer is preferably 5% by weight or more, preferably It is 10% by weight or more and 50% by weight or less, preferably about 30% by weight or less.
Further, the volume average particle size of the filler used is preferably in the range of 0.1 μm to 2 μm, and preferably in the range of 0.3 μm to 1 μm. In this case, if the average particle size is too small, the wear resistance is not sufficiently exhibited, and if it is too large, the surface property of the coating film is deteriorated or the coating film itself cannot be formed.

The average particle diameter of the filler in the present invention is a volume average particle diameter unless otherwise specified, and is determined by an ultracentrifugal automatic particle size distribution analyzer: CAPA-700 (manufactured by Horiba). At this time, the particle size (Median system) corresponding to 50% of the cumulative distribution was calculated. In addition, it is important that the standard deviation of each particle measured simultaneously is 1 μm or less. If the standard deviation is larger than this, the particle size distribution may be too wide, and the effects of the present invention may not be obtained remarkably.
Further, the pH of the filler used in the present invention greatly affects the resolution and the dispersibility of the filler. One possible reason is that hydrochloric acid or the like remains in the filler, particularly the metal oxide, during production. When the remaining amount is large, the occurrence of image blur is unavoidable, and depending on the remaining amount, the dispersibility of the filler may be affected.

  Another reason is due to the difference in chargeability on the surface of the filler, particularly the metal oxide. Usually, particles dispersed in a liquid are charged positively or negatively, and ions having opposite charges gather to try to keep it electrically neutral, and an electric double layer is formed there. The dispersed state of the particles is stabilized. The potential (zeta potential) gradually decreases with increasing distance from the particle, and the potential in a region that is sufficiently away from the particle and electrically neutral is zero. Therefore, the stability increases as the repulsive force of the particles increases due to an increase in the absolute value of the zeta potential, and the particles tend to aggregate and become unstable as they approach zero. On the other hand, the zeta potential varies greatly depending on the pH value of the system, and at a certain pH value, the potential becomes zero and has an isoelectric point. Therefore, the dispersion system is stabilized by increasing the absolute value of the zeta potential as far as possible from the isoelectric point of the system.

In the configuration of the present invention, the filler having a pH at the isoelectric point of at least 5 is preferably from the viewpoint of image blur suppression, and the more basic the filler, the higher the effect. It was confirmed that there was. A filler exhibiting basicity having a high pH at the isoelectric point has a higher zeta potential when the system is acidic, thereby improving dispersibility and its stability.
Here, the pH of the filler in the present invention is the pH value at the isoelectric point from the zeta potential. At this time, the zeta potential was measured with a laser zeta potentiometer manufactured by Otsuka Electronics Co., Ltd.

Furthermore, as the filler that is less likely to cause image blurring, a filler having high electrical insulation (specific resistance is 10 ¹⁰ Ω · cm or more) is preferable, and the filler having a pH of 5 or more or the filler having a dielectric constant of 5 or more. The ones shown can be used particularly effectively. In addition, a filler having a pH of 5 or more or a filler having a dielectric constant of 5 or more can be used alone, or two or more fillers having a pH of 5 or less and a filler having a pH of 5 or more can be mixed. It is also possible to use a mixture of two or more fillers having a dielectric constant of 5 or less and a filler having a dielectric constant of 5 or more. Among these fillers, α-type alumina, which has high insulation properties, high thermal stability, and high wear resistance, is a hexagonal close-packed structure, from the viewpoint of suppressing image blur and improving wear resistance. It is particularly useful.

The specific resistance of the filler used in the present invention is defined as follows. Since the specific resistance value of a powder such as a filler varies depending on the filling rate, it is necessary to measure under certain conditions. In the present invention, the specific resistance value of the filler is determined using an apparatus having the same configuration as the measuring apparatus shown in Japanese Patent Laid-Open Nos. 5-94049 (FIG. 1) and 5-113688 (FIG. 1). Measured and used this value. In the measuring device, the electrode area is 4.0 cm ² . Prior to measurement, a load of 4 kg is applied to one electrode for 1 minute, and the sample amount is adjusted so that the distance between the electrodes is 4 mm. At the time of measurement, the measurement is performed with the weight of the upper electrode (1 kg) loaded, and the applied voltage is measured at 100V. The area of 10 ⁶ Ω · cm or more was measured with a HIGH RESISTER METER (Yokogawa Hewlett Packard), and the area below it was measured with a digital multimeter (Fluke). The specific resistance value thus obtained is defined as the specific resistance value in the present invention.

  The dielectric constant of the filler was measured as follows. Using a cell similar to the measurement of the specific resistance as described above, after applying a load, the capacitance was measured, and the dielectric constant was determined from this. For the measurement of the capacitance, a dielectric loss measuring device (Ando Electric) was used.

  Further, 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, all conventionally used surface treatment agents can be used, but a surface treatment agent capable of maintaining the insulating properties of the filler is preferable. For example, a titanate coupling agent, an aluminum coupling agent, a zircoaluminate coupling agent, a higher fatty acid, etc., or a mixing treatment of these with a silane coupling agent, Al ₂ O ₃ , TiO ₂ , ZrO ₂ , Silicone, aluminum stearate, or the like, or a mixture thereof is more preferable from the viewpoint of filler dispersibility and image blur.

  The treatment with the silane coupling agent is strongly influenced by image blur, but the influence may be suppressed by performing a mixing treatment of the surface treatment agent and the silane coupling agent.

  The surface treatment amount varies depending on the average primary particle size of the filler used, but is preferably 3 to 30 wt%, more preferably 5 to 20 wt%. 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 surface treatment amount of the filler is defined by the weight ratio of the surface treatment agent to be used with respect to the filler amount as described above.

  Further, these filler materials can be dispersed by using an appropriate disperser. Further, from the viewpoint of the transmittance of the protective layer, it is preferable that the filler used is dispersed to the primary particle level and has less aggregates.

  Further, the protective layer (39) may contain a charge transport material for reducing residual potential and improving responsiveness. As the charge transport material, the materials described in the description of the charge transport layer can be used. When a low molecular charge transport material is used as the charge transport material, a concentration gradient in the protective layer may be provided. In order to improve wear resistance, it is an effective means to reduce the concentration of the surface side. The concentration here refers to the ratio of the weight of the low molecular charge transporting material to the total weight of all the materials constituting the protective layer, and the concentration gradient is a gradient that lowers the concentration on the surface side in the above weight ratio. It shows that. The use of a polymer charge transport material is very advantageous in terms of enhancing the durability of the photoreceptor.

  As a method for forming the protective layer, a normal coating method is employed. In addition, about 0.1-10 micrometers is suitable for the thickness of a protective layer. In addition to the above, a known material such as a-C or a-SiC formed by a vacuum thin film forming method can be used as the protective layer.

In addition, as the binder resin for the protective layer, the polymer charge transport material described in the section of the charge transport layer can be used. As the effect when this is used, the effect of improving the wear resistance and the high-speed charge transport can be obtained as described in the section of the charge transport layer.
Moreover, the protective layer which consists of a crosslinked structure is also used effectively as a binder structure of a protective layer. Regarding the formation of a cross-linked structure, a reactive monomer having a plurality of cross-linkable functional groups in one molecule is used to cause a cross-linking reaction using light or thermal energy to form a three-dimensional network structure. is there. This network structure functions as a binder resin and exhibits high wear resistance.

  Moreover, it is a very effective means to use a monomer having a charge transporting ability in whole or in part as the reactive monomer. By using such a monomer, a charge transporting site is formed in the network structure, and the function as a protective layer can be sufficiently expressed. A reactive monomer having a triarylamine structure is effectively used as the monomer having charge transporting ability.

  The charge transport layer having such a network structure has high wear resistance, but has a large volume shrinkage during the crosslinking reaction, and if it is too thick, cracks may occur. In such a case, the protective layer may be a laminated structure, a low molecular dispersion polymer protective layer may be used for the lower layer (photosensitive layer side), and a protective layer having a crosslinked structure may be formed on the upper layer (surface side). good.

  As described above, the use of a polymer charge transport material for the photosensitive layer (charge transport layer) or the provision of a protective layer on the surface of the photoreceptor increases the durability (wear resistance) of each photoreceptor. In addition, when used in a tandem type full-color image forming apparatus as described later, a new effect not found in the monochrome image forming apparatus is also produced.

In the case of a full-color image, various types of images are input, but on the contrary, a typical image may also be input. For example, the presence of a seal in a Japanese document or the like. Something like indicia is usually located towards the edge of the image area, and the colors used are also limited. In a state in which a random image is always written, image writing, development, and transfer are performed on the photoconductor in the image forming element on average. When many image formations are repeated or only a specific image forming element is used, the durability balance is lost.
When a photoconductor having a low surface durability (physical / chemical / mechanical) is used in such a state, this difference becomes prominent and easily causes an image problem. On the other hand, when the photoconductor is made highly durable, the amount of such local change is small, and as a result, it becomes difficult to appear as a defect on the image, so that high durability is achieved and the stability of the output image is improved. This is very effective.

  Hereinafter, although an example is given and the present invention is explained, the present invention is not restricted by an example. All parts are parts by weight.

First, a synthesis example of a charge generation material (titanyl phthalocyanine crystal) will be described.
(Comparative Synthesis Example 1)
A pigment was prepared according to Japanese Patent Application Laid-Open No. 2001-19871. That is, 29.2 g of 1,3-diiminoisoindoline and 200 ml of sulfolane are mixed, and 20.4 g of titanium tetrabutoxide is added dropwise under a nitrogen stream. After completion of the dropwise addition, the temperature was gradually raised to 180 ° C., and the reaction was carried out by stirring for 5 hours while maintaining the reaction temperature between 170 ° C. and 180 ° C. After completion of the reaction, the mixture was allowed to cool, and then the precipitate was filtered, washed with chloroform until the powder turned blue, then washed several times with methanol, further washed several times with hot water at 80 ° C., and dried. Crude titanyl phthalocyanine was obtained. Dissolve the crude titanyl phthalocyanine in 20 times the amount of concentrated sulfuric acid, add dropwise to 100 times the amount of ice water with stirring, filter the precipitated crystals, and then repeat washing with water until the washing solution becomes neutral. (Water paste) was obtained. 2 g of the obtained wet cake (water paste) was put into 20 g of tetrahydrofuran, stirred for 4 hours, filtered and dried to obtain titanyl phthalocyanine powder.
Further, 30 g of this titanyl phthalocyanine crystal was immersed in 300 g of tetrahydrofuran, and a second crystal conversion was performed. After leaving it immersed for 12 hours, it was separated by filtration and dried under reduced pressure under the same conditions as above to obtain a titanyl phthalocyanine crystal used in the present invention. This is designated as Pigment 1. (Referred to as pigment 1).

(Synthesis Example 1)
In accordance with the method of Comparative Synthesis Example 1, a titanyl phthalocyanine pigment water paste was synthesized, and crystal conversion was performed as follows to obtain phthalocyanine crystals having smaller primary particles than Comparative Synthesis Example 1.
To 60 parts of the water paste before crystal conversion obtained in Comparative Synthesis Example 1, 1500 parts of tetrahydrofuran was added and stirred vigorously (2000 rpm) with a homomixer (Kennis, MARKIIf model) at room temperature. When the color changed to light blue (20 minutes after the start of stirring), stirring was stopped and filtration under reduced pressure was immediately performed. The crystals obtained on the filter were washed with tetrahydrofuran to obtain a pigment wet cake. This was dried under reduced pressure (5 mmHg) at 70 ° C. for 2 days to obtain 58 parts of titanyl phthalocyanine crystals.
Further, 30 g of this titanyl phthalocyanine crystal was immersed in 300 g of tetrahydrofuran, and a second crystal conversion was performed. After leaving it immersed for 12 hours, it was separated by filtration and dried under reduced pressure under the same conditions as above to obtain a titanyl phthalocyanine crystal used in the present invention. This is designated as Pigment 2.
(Synthesis Example 2)
The treatment was performed in the same manner as in Synthesis Example 1 except that the second crystal conversion operation in Synthesis Example 1 was changed to the following conditions to obtain a titanyl phthalocyanine crystal of the present invention (see FIG. 14). This is designated as Pigment 3.

(Second crystal conversion process)
30 g of titanyl phthalocyanine crystals subjected to the first crystal conversion treatment were subjected to mechanical shearing force for 5 minutes by a commercially available mixer, and then the powder was taken out.

(Synthesis Example 3)
The treatment was performed in the same manner as in Synthesis Example 1 except that the second crystal conversion operation in Synthesis Example 1 was changed to the following conditions to obtain a titanyl phthalocyanine crystal of the present invention. This is designated as Pigment 4.
(Second crystal conversion process)
30 g of titanyl phthalocyanine crystals subjected to the first crystal conversion treatment were put into a φ90 mm glass pot together with 2 kg of φ6 mm zirconia balls, and after dry milling for 10 minutes, the powder was taken out.

(Comparative Synthesis Example 2)
The treatment was performed in the same manner as in Synthesis Example 1 except that the second crystal conversion solvent in Synthesis Example 1 was changed from tetrahydrofuran to methanol to obtain titanyl phthalocyanine crystals. This is designated as Pigment 5.

(Comparative Synthesis Example 3)
In Comparative Synthesis Example 1, treatment was performed in the same manner as in Comparative Synthesis Example 1 except that 2-butanone was used in place of tetrahydrofuran as the first crystal conversion solvent and the second crystal conversion was not performed, and the titanyl phthalocyanine crystals were obtained. Obtained. This is designated as Pigment 6.

The titanyl phthalocyanine powder obtained as described above was subjected to X-ray diffraction spectrum measurement under the following conditions.
(X-ray diffraction spectrum measurement conditions)
X-ray tube: Cu
Voltage: 50kV
Current: 30mA
Scanning speed: 2 ° / min Scanning range: 3 ° -40 °
Time constant: 2 seconds

The pigments 1 to 4 obtained from Comparative Synthesis Example 1 and Synthesis Examples 1 to 3 showed the same X-ray diffraction spectrum in all cases except for the peak intensity of 26.3 °. The X-ray diffraction spectrum of the titanyl phthalocyanine crystal obtained in Example 2 is shown in FIG. 14 (the arrow in the figure is a peak at 26.3 °, and the peak intensity ratio is 8%).
Bragg angle 2θ with respect to Cu-Kα ray (wavelength 1.542 mm) has a maximum peak at 27.2 ± 0.2 ° and a peak at minimum angle 7.3 ± 0.2 °, and a peak at 7.3 ° It can be seen that this is a titanyl phthalocyanine powder having no peak between 1 and 9.4 ° and further having a peak at 26.3 °.
A part of the water paste obtained in Comparative Synthesis Example 1 was dried at 80 ° C. under reduced pressure (5 mmHg) for 2 days to obtain a low crystalline titanyl phthalocyanine powder. The X-ray diffraction spectrum of the dry powder of water paste is shown in FIG.

The X-ray diffraction spectrum of the titanyl phthalocyanine crystal (pigment 5) obtained in Comparative Synthesis Example 2 is shown in FIG. 16, but no peak was observed at 26.3 °.
The X-ray diffraction spectrum of the titanyl phthalocyanine crystal (pigment 6) obtained in Comparative Synthesis Example 3 is shown in FIG. 17, and the lowest angle exists at 7.5 °.
A portion of titanyl phthalocyanine (water paste) before crystal transformation prepared in Comparative Synthesis Example 1 was diluted with ion-exchanged water to approximately 1% by weight, and the surface was scooped with a copper net having been subjected to conductive treatment. The particle size of phthalocyanine was observed with a transmission electron microscope (TEM, Hitachi: H-9000NAR) at a magnification of 75000 times. The average particle size was determined as follows.

The TEM image observed as described above is taken as a TEM photograph, and 30 titanyl phthalocyanine particles (a shape close to a needle shape) projected are arbitrarily selected, and the size of each major axis is measured. The arithmetic average of the major diameters of the 30 individuals measured was determined as the average particle size.
The average particle size in the water paste in Synthesis Example 1 determined by the above method was 0.06 μm.

  In addition, the titanyl phthalocyanine crystal after crystal conversion just before filtration in Comparative Synthesis Example 1 and Synthesis Example 1 was diluted with tetrahydrofuran to about 1% by weight, and observed in the same manner as the above method. The average particle size obtained as described above is shown in Table 1. In addition, the titanyl phthalocyanine crystal produced in Comparative Synthesis Example 1 and Synthesis Example 1 did not necessarily have the same shape of all crystals (a shape close to a triangle, a shape close to a square, etc.). For this reason, the calculation was performed with the length of the largest diagonal line of the crystal as the major axis.

(Comparative Synthesis Example 4)
A pigment was prepared according to the method described in Example 1 of JP-A-1-299874 (Patent No. 2512081). That is, the wet cake produced in the previous Comparative Synthesis Example 1 was dried, 1 g of the dried product was added to 50 g of polyethylene glycol, and sand milling was performed with 100 g of glass beads. After the crystal transition, the mixture was washed successively with dilute sulfuric acid and aqueous ammonium hydroxide and dried to obtain a pigment. This is designated as Pigment 7.

(Comparative Synthesis Example 5)
A pigment was produced according to the method described in Production Example 1 of JP-A-3-269064 (Patent No. 2854682). That is, the wet cake prepared in Comparative Synthesis Example 1 was dried, and 1 g of the dried product was stirred (50 ° C.) in a mixed solvent of 10 g of ion-exchanged water and 1 g of monochlorobenzene for 1 hour, and then methanol and ion-exchanged water. The pigment was obtained by washing and drying. This is designated as Pigment 8.

(Comparative Synthesis Example 6)
A pigment was produced according to the method described in the production example of JP-A-2-8256 (Japanese Patent Publication No. 7-91486). That is, 9.8 g of phthalodinitrile and 75 ml of 1-chloronaphthalene are stirred and mixed, and 2.2 ml of titanium tetrachloride is added dropwise under a nitrogen stream. After completion of the dropping, the temperature was gradually raised to 200 ° C., and the reaction was carried out by stirring for 3 hours while maintaining the reaction temperature between 200 ° C. and 220 ° C. After completion of the reaction, the mixture was allowed to cool to 130 ° C. and filtered while hot, then washed with 1-chloronaphthalene until the powder turned blue, then washed several times with methanol, and further with hot water at 80 ° C. After washing twice, it was dried to obtain a pigment. This is designated as Pigment 9.

(Comparative Synthesis Example 7)
A pigment was produced according to the method described in Synthesis Example 1 of JP-A No. 64-17066 (Japanese Patent Publication No. 7-97221). That is, 5 parts of α-type TiOPc was subjected to crystal conversion treatment at 100 ° C. for 10 hours with a sand grinder together with 10 g of sodium chloride and 5 g of acetophenone. This was washed with ion-exchanged water and methanol, purified with dilute sulfuric acid aqueous solution, washed with ion-exchanged water until the acid content disappeared, and dried to obtain a pigment. This is designated as Pigment 10.

(Comparative Synthesis Example 8)
A pigment was prepared according to the method described in Example 1 of JP-A-11-5919 (Japanese Patent No. 3003664). That is, after 20.4 parts of o-phthalodinitrile and 7.6 parts of titanium tetrachloride were heated in 50 parts of quinoline at 200 ° C. for 2 hours, the solvent was removed by steam distillation, followed by a 2% aqueous chloride solution, The product was purified with a 2% aqueous sodium hydroxide solution, washed with methanol and N, N-dimethylformamide, and then dried to obtain titanyl phthalocyanine. 2 parts of this titanyl phthalocyanine is dissolved little by little in 40 parts of 98% sulfuric acid at 5 ° C., and the mixture is stirred for about 1 hour while maintaining the temperature at 5 ° C. or less. Subsequently, the sulfuric acid solution is slowly poured into 400 parts of ice water stirred at a high speed, and the precipitated crystals are filtered. The crystals are washed with distilled water until no acid remains, and a wet cake is obtained. The cake was stirred in 100 parts of THF for about 5 hours, filtered, washed with THF and dried to obtain a pigment. This is designated as Pigment 11.

(Comparative Synthesis Example 9)
A pigment was produced according to the method described in Synthesis Example 2 of JP-A-3-255456 (Patent No. 3005052). That is, 10 parts of the wet cake prepared in the previous Comparative Synthesis Example 1 was mixed with 15 parts of sodium chloride and 7 parts of diethylene glycol, and milled for 60 hours with an automatic mortar under heating at 80 ° C. Next, sufficient washing was performed to completely remove sodium chloride and diethylene glycol contained in the treated product. After drying this under reduced pressure, 200 parts of cyclohexanone and glass beads having a diameter of 1 mm were added, and the mixture was treated with a sand mill for 30 minutes to obtain a pigment. This is designated as Pigment 12.

(Comparative Synthesis Example 10)
A pigment was prepared according to the method described in Example 4 of JP-A-11-5919 (Japanese Patent No. 3003664). That is, the wet cake obtained in the previous Comparative Synthesis Example 8 was washed with 5% hydrochloric acid, washed with water and filtered until neutral, and dried. Further, this was dispersed with THF in a ball mill for 10 hours, filtered and dried to obtain a pigment powder. This is designated as Pigment 13.

(Comparative Synthesis Example 11)
A pigment was produced according to the method described in Production Example 1 and Production Example 2 of JP-A-5-134437 (Patent No. 3196260).
That is, 97.5 g of phthalodinitrile is added to 750 ml of α-chloronaphthalene, and then 22 ml of titanium tetrachloride is added dropwise under a nitrogen atmosphere. After dropping, the temperature was raised, and the mixture was reacted at 200 to 220 ° C. for 3 hours with stirring, then allowed to cool, filtered hot at 100 to 130 ° C., and washed with 200 ml of α-chloronaphthalene heated to 100 ° C. Furthermore, the hot-washing process (100 degreeC, 1 hour) was performed 3 times with 200 ml N-methylpyrrolidone. Subsequently, the suspension was washed with 300 ml of methanol at room temperature, and further washed with 500 ml of methanol for 1 hour. This is designated as phthalocyanine 1.
Next, phthalocyanine 1 was ground in a sand grind mill for 20 hours, then placed in a suspension of 400 ml of water and 40 ml of o-dichlorobenzene, and heat-treated at 60 ° C. for 1 hour. This is designated as phthalocyanine 2.
Further, according to Example 1 of JP-A-5-134437, 6 parts and 4 parts of phthalocyanine 1 and phthalocyanine 2 were mixed, 200 parts of n-propanol was added, and pulverized and atomized in a sand grind mill for 10 hours. Distributed processing was performed. This was dried to obtain phthalocyanine powder. This is designated as Pigment 14.

(Comparative Synthesis Example 12)
A pigment was prepared according to the method for producing a titanyl phthalocyanine crystal of JP-A-8-110649. That is, 58 g of 1,3-diiminoisoindoline and 51 g of tetrabutoxy titanium were reacted in 210 mL of α-chloronaphthalene at 210 ° C. for 5 hours, and then washed in the order of α-chloronaphthalene and dimethylformamide (DMF). Thereafter, it was washed with hot DMF, hot water and methanol and dried to obtain 50 g of titanyl phthalocyanine. 4 g of titanyl phthalocyanine was added to 400 g of sulfuric acid cooled to 0 ° C., followed by stirring at 0 ° C. for 1 hour. After confirming that phthalocyanine was completely dissolved, it was added to a 800 mL water / 800 mL toluene mixture cooled to 0 ° C. After stirring at room temperature for 2 hours, the precipitated phthalocyanine crystal was separated from the mixture and washed with methanol and water in this order. After confirming the neutrality of the washing water, the phthalocyanine crystal was separated from the washing water and dried to obtain 2.9 g of titanyl phthalocyanine crystal. This is designated as Pigment 15.

  The pigments 7 to 15 prepared in the above Comparative Synthesis Examples 4 to 12 were measured for X-ray diffraction spectra by the same method as described above, and confirmed to be the same as the spectra described in the respective publications. Table 2 shows the characteristics of the peak positions of the X-ray diffraction spectra of the pigments 1 to 15.

(Dispersion Preparation Example 1)
Pigment 1 prepared in Comparative Synthesis Example 1 was dispersed under the following composition under the following conditions to prepare a dispersion as a charge generation layer coating solution.
Titanyl phthalocyanine pigment (Pigment 1) 15 parts Polyvinyl butyral (manufactured by Sekisui Chemical: BX-1) 10 parts 2-butanone 280 parts A commercially available bead mill disperser was used to dissolve polyvinyl butyral using PSZ balls having a diameter of 0.5 mm All butanone and pigment were added, and the rotor rotation speed was 1200 r. p. m. And dispersion was performed for 30 minutes to prepare a dispersion (referred to as dispersion 1).

(Dispersion Preparation Examples 2 to 15)
In place of Pigment 1 used in Dispersion Preparation Example 1, pigments 2 to 15 prepared in Synthesis Examples 1 to 3 and Comparative Synthesis Examples 2 to 12 were used, respectively, and dispersed under the same conditions as Dispersion Preparation Example 1. Liquids were prepared (corresponding to the pigment numbers, dispersions 2 to 15, respectively).

(Dispersion Preparation Example 16)
The dispersion 1 prepared in Dispersion Preparation Example 1 was filtered using a cotton wind cartridge filter, TCW-1-CS (effective pore size 1 μm) manufactured by Advantech. In the filtration, a pump was used and filtration was performed under pressure (referred to as dispersion liquid 16).

(Dispersion Preparation Example 17)
Dispersion was performed by pressure filtration in the same manner as in Dispersion Preparation Example 16 except that the filter used in Dispersion Preparation Example 16 was changed to a cotton wind cartridge filter manufactured by Advantech, TCW-3-CS (effective pore size 3 μm). A liquid was prepared (referred to as dispersion liquid 17).

(Dispersion Preparation Example 18)
Dispersion was performed by pressure filtration in the same manner as in Dispersion Preparation Example 16, except that the filter used in Dispersion Preparation Example 15 was changed to an Advantech Co., Ltd. cotton wind cartridge filter, TCW-5-CS (effective pore size 5 μm). A liquid was prepared (referred to as dispersion 18).

(Dispersion Preparation Example 19)
Dispersion was carried out by changing the dispersion conditions in Dispersion Preparation Example 1 as follows (referred to as Dispersion 19).
Rotor rotation speed: 1000 r. p. m. For 20 minutes.

(Dispersion Preparation Example 20)
The dispersion prepared in Dispersion Preparation Example 19 was filtered using a cotton wind cartridge filter, TCW-1-CS (effective pore size 1 μm) manufactured by Advantech. During filtration, a pump was used and filtration was performed in a pressurized state. During the filtration, the filter was clogged, and it was not possible to filter all the dispersions. Therefore, the following evaluation has not been conducted.
The particle size distribution of the pigment particles in the dispersion prepared as described above was measured by HORIBA, Ltd .: CAPA-700. The results are shown in Table 3.

(Photoreceptor Preparation Example 1)
An undercoat layer coating solution, a charge generation layer coating solution, and a charge transport layer coating solution having the following composition were sequentially applied and dried on an aluminum cylinder (JIS1050) having a diameter of 100 mm, and an undercoat layer of 3.5 μm, A charge generation layer and a 27 μm charge transport layer were formed to produce a laminated photoreceptor (referred to as photoreceptor 1). The film thickness of the charge generation layer was adjusted so that the transmittance of the charge generation layer at 780 nm was 20%. The charge generation layer transmittance was measured by applying a charge generation layer coating solution having the following composition to an aluminum cylinder wrapped with a polyethylene terephthalate film under the same conditions as the preparation of the photoreceptor, and coating the charge generation layer as a comparative control. The transmittance was measured at 780 nm using a commercially available spectrophotometer (Shimadzu: UV-3100).

(Undercoat layer coating solution)
Titanium oxide (CR-EL: manufactured by Ishihara Sangyo Co., Ltd.) 70 parts Alkyd resin 15 parts (Beckolite M6401-50-S (solid content 50%)
Dainippon Ink & Chemicals)
Melamine resin 10 parts (Super Becamine L-121-60 (solid content 60%)
Dainippon Ink & Chemicals)
2-butanone 100 parts

(Charge generation layer coating solution)
The previously prepared dispersion 1 was used.

(Charge transport layer coating solution)
Polycarbonate (TS2050: manufactured by Teijin Chemicals Ltd.) 10 parts 7 parts of charge transport material having the following structural formula
80 parts of methylene chloride

(Photosensitive member production examples 2 to 19)
A photoconductor was prepared in the same manner as in Photoconductor Preparation Example 1 except that the charge generation layer coating liquid (dispersion 1) used in Photoconductor Preparation Example 1 was changed to dispersions 2 to 19, respectively. In addition, the film thickness of the charge generation layer was adjusted so that the transmittance at 780 nm was 20% when all the coating liquids were used, as in Photoreceptor Preparation Example 1.

(Examples 1 to 3, Reference Examples 1 and 2, and Comparative Examples 1 to 33)
The electrophotographic photoconductors of photoconductor production examples 1 to 19 produced as described above are mounted on the image forming apparatus shown in FIG. 3 (photoconductor linear velocity is 320 mm / sec), and a scorotron charging member is used as follows. Charging under charging conditions, image exposure light source is 780nm semiconductor laser (image writing by polygon mirror, resolution 600dpi), transfer belt is used as transfer member, and 100,000 sheets are printed continuously using a chart with a writing rate of 6% (The test environment is 22 ° C.-55% RH).

Charging condition 1:
Discharge voltage: -6.0 kV
Grid voltage: -920V (surface potential of unexposed portion of photoconductor is -900V)

Charging condition 2:
Discharge voltage: -5.8 kV
Grid voltage: -780V (surface potential of unexposed portion of photoconductor is -750V)
The following two evaluations were carried out after printing 100,000 sheets of images.
(I) Evaluation of soiling:
A white solid image was output, and rank evaluation was performed from the number and size of black spots generated on the background.
(Ii) Evaluation of dot formation state A 1-dot image having a diameter of 60 μm was formed, and the dot formation state was observed with a 150 × microscope.
Rank evaluation was conducted.
In each case, the rank evaluation was performed in 4 stages, and very good ones were indicated by ◎, good ones by ○, slightly inferior by Δ, and very bad by x. The above results are shown in Tables 4 and 5.

Further, after the above test at 22 ° C.-55% RH, the above charging conditions remain unchanged (charging conditions are only condition 1), 20,000 sheets at 10 ° C.-15% RH, and 2 at 30 ° C.-90% RH. Ten thousand running tests were conducted, and the images after 20,000 images were evaluated in the same manner. The results are shown in Tables 6 to 9, respectively.
In the calculation of the electric field strength, the film thickness of the charge generation layer was about 0.1 μm, but the calculation was performed assuming that the film thickness of the photosensitive layer is equal to the film thickness of the charge transport layer.

<Evaluation results under 22 ° C.-55% RH environment>

<Evaluation results under 22 ° C.-55% RH environment>

<Evaluation results under 10 ° C-15% RH environment>

The images of Examples 1 to 3 and Reference Examples 1 and 2 were all good images, but in the image after 20,000 sheets in a 10 ° C.-15% RH environment, the image of Example 2 was Compared with the images of Example 1 and Example 3 and Reference Examples 1 and 2 , the image density was low.

<Evaluation results in a 30 ° C.-90% RH environment>

<Evaluation results in a 30 ° C.-90% RH environment>
(Photoreceptor Preparation Example 20)
A photoconductor was prepared in the same manner as in Photoconductor Preparation Example 2, except that the charge transport layer coating solution in Photoconductor Preparation Example 2 was changed to one having the following composition.
(Charge transport layer coating solution)
10 parts of polymer charge transport material with the following composition
(Weight average molecular weight: about 135000)
0.5 parts of additive with the following structure
100 parts of methylene chloride (Photoconductor Preparation Example 21)
Similar to Photoconductor Preparation Example 2 except that the thickness of the charge transport layer in Photosensitive Member Preparation Example 2 was 21 μm, a protective layer coating solution having the following composition was applied and dried on the charge transport layer, and a protective layer of 5 μm was provided. A photoreceptor was prepared.

(Protective layer coating solution)
Polycarbonate (TS2050: manufactured by Teijin Chemicals Ltd.) 10 parts 7 parts of charge transport material having the following structural formula
4 parts of alumina fine particles (specific resistance: 2.5 × 10 ¹² Ω · cm, average primary particle size: 0.4 μm)
Cyclohexanone 500 parts Tetrahydrofuran 150 parts

(Photoconductor Preparation Example 22)
A photoconductor was prepared in the same manner as in Photoconductor Preparation Example 21, except that the alumina fine particles in the protective layer coating solution in Photoconductor Preparation Example 21 were changed to the following.
4 parts of titanium oxide fine particles (specific resistance: 1.5 × 10 ¹⁰ Ω · cm, average primary particle size: 0.5 μm)

(Photoconductor Preparation Example 23)
A photoconductor was prepared in the same manner as in Photoconductor Preparation Example 21, except that the alumina fine particles in the protective layer coating solution in Photoconductor Preparation Example 21 were changed to the following.
4 parts of tin oxide-antimony oxide powder (specific resistance: 10 ⁶ Ω · cm, average primary particle size 0.4 μm)

(Photoconductor Preparation Example 24)
An electrophotographic photosensitive member was prepared in the same manner as in the photosensitive member preparation example 21 except that the protective layer coating solution in the photosensitive member preparation example 21 was changed to one having the following composition.
(Protective layer coating solution)
17 parts of a polymeric charge transport material having the following structural formula: “As measured by GPC, n was determined to be about 250”
4 parts of alumina fine particles (specific resistance: 2.5 × 10 ¹² Ω · cm, average primary particle size: 0.4 μm)
Cyclohexanone 500 parts Tetrahydrofuran 150 parts

(Photoconductor Preparation Example 25)
An electrophotographic photosensitive member was prepared in the same manner as in the photosensitive member preparation example 21 except that the protective layer coating solution in the photosensitive member preparation example 21 was changed to one having the following composition.
(Protective layer coating solution)
Methyltrimethoxysilane 100 parts 3% acetic acid 20 parts 35 parts of a charge transporting compound having the following structure
Antioxidant (Sanol LS2626: Sankyo Chemical Co., Ltd.) 1 part Curing agent (dibutyltin acetate) 1 part 2-propanol 200 parts

(Photoconductor Preparation Example 26)
An electrophotographic photosensitive member was prepared in the same manner as in the photosensitive member preparation example 21 except that the protective layer coating solution in the photosensitive member preparation example 21 was changed to one having the following composition.

(Protective layer coating solution)
Methyltrimethoxysilane 100 parts 3% acetic acid 20 parts 35 parts of a charge transporting compound having the following structure
α-alumina particles (Sumicorundum AA-03: manufactured by Sumitomo Chemical Co., Ltd.) 15 parts Antioxidant (Sanol LS2626: manufactured by Sankyo Chemical Co., Ltd.) 1 part polycarboxylic acid compound BYK P104: 0.4 parts manufactured by BYK Chemie Co., Ltd. Curing agent (dibutyl) Tin acetate) 1 part 2-propanol 200 parts

(Photoconductor Preparation Example 27)
The aluminum cylinder (JIS 1050) in photoreceptor preparation example 2 is subjected to the following anodic oxide film treatment, and then a charge generation layer and a charge transport layer are provided in the same manner as in photoreceptor preparation example 2 without providing an undercoat layer. Was made.

(Anodized film treatment)
The surface of the support was mirror polished, degreased and washed with water, then immersed in an electrolytic bath of 20 ° C. and 15 vol% sulfuric acid, and anodized film treatment was performed for 30 minutes at an electrolysis voltage of 15V. Further, after washing with water, sealing treatment was performed with a 7% nickel acetate aqueous solution (50 ° C.). Thereafter, the substrate was washed with pure water to obtain a support on which a 7 μm anodic oxide film was formed.

(Examples 4 to 11 and Comparative Examples 34 to 40)
As described above, the electrophotographic photoreceptors produced in the photoreceptor preparation examples 20 to 27 are mounted on the image forming apparatus shown in FIG. 3 (photoconductor linear velocity is 320 mm / sec), and the following is used using a scorotron charging member. Charging under charging conditions, image exposure light source is 780nm semiconductor laser (image writing by polygon mirror, resolution 600dpi), transfer belt is used as transfer member, and 100,000 sheets are printed continuously using a chart with a writing rate of 6% (The test environment is 22 ° C.-55% RH).

Charging condition 1:
Discharge voltage: -6.0 kV
Grid voltage: -920V (surface potential of unexposed portion of photoconductor is -900V)

Charging condition 2:
Discharge voltage: -5.8 kV
Grid voltage: -780V (surface potential of unexposed portion of photoconductor is -750V)
The following two evaluations were carried out after printing 100,000 sheets of images.
(I) Evaluation of soiling:
A white solid image was output, and rank evaluation was performed from the number and size of black spots generated on the background.
(Ii) Evaluation of dot formation state A one-dot image having a diameter of 60 μm was formed, and the dot formation state was observed with a 150 × microscope, and rank evaluation was performed.
In each case, the rank evaluation was performed in 4 stages, and very good ones were indicated by ◎, good ones by ○, slightly inferior by Δ, and very bad by x. In addition, the amount of abrasion of the photosensitive layer after printing 100,000 sheets (the amount of abrasion of the protective layer when a protective layer is provided) was measured. The results are shown in Table 10 together with the case of Example 1.

(Comparative Example 42)
In Example 1, the charging member of the image forming apparatus was changed from a scorotron charging member to a contact charging charging roller (φ30 mm). Evaluation was performed in the same manner as in Example 1 except that charging was performed under the following conditions.
Charging conditions:
DC bias: -1600 V (Adjusted so that the surface potential of the unexposed portion of the photoreceptor is -900 V)

(Comparative Example 43)
In Example 1, the charging member of the image forming apparatus was changed from a scorotron charging member to a contact charging charging roller (φ30 mm). Evaluation was performed in the same manner as in Example 1 except that charging was performed under the following conditions.
Charging conditions:
DC bias: -900V
AC bias: 2.0 kV (peak to peak), frequency: 3.0 kHz
The above results are shown in Table 11 together with the results of Example 1.
Compared with the image of the first embodiment, in the case of the comparative example 42, the charging unevenness is remarkable and a clear image is not output. This tendency was particularly noticeable in halftone images.
On the other hand, in the case of Comparative Example 43, it was seen that the charging uniformity was ensured to some extent, but the amount of wear was large, and the background stain was severe in the image after 100,000 sheets.

(Photoreceptor Preparation Example 28)
The aluminum cylinder of the photoreceptor preparation example 1 was changed to one having a diameter of 60 mm, and a photoreceptor having the same composition as that of the photoreceptor preparation example 1 was prepared.

(Photoconductor Preparation Example 29)
The aluminum cylinder of the photoreceptor preparation example 2 was changed to one having a diameter of 60 mm, and a photoreceptor having the same composition as that of the photoreceptor preparation example 2 was prepared.

(Photoreceptor Preparation Example 30)
The aluminum cylinder of the photoreceptor preparation example 4 was changed to one having a diameter of 60 mm to prepare a photoreceptor having the same composition as the photoreceptor preparation example 4.

(Photoreceptor Preparation Example 31)
The aluminum cylinder of the photoreceptor preparation example 13 was changed to one having a diameter of 60 mm, and a photoreceptor having the same composition as that of the photoreceptor preparation example 13 was prepared.

(Photoconductor Preparation Example 32)
A photoconductor having the same composition as that of Photoconductor Preparation Example 14 was prepared by changing the aluminum cylinder of Photoconductor Preparation Example 14 to one having a diameter of 60 mm.

(Photoconductor Preparation Example 33)
A photoconductor having the same composition as that of Photoconductor Preparation Example 15 was prepared by changing the aluminum cylinder of Photoconductor Preparation Example 15 to one having a diameter of 60 mm.

(Examples 12 to 13 and Comparative Examples 44 to 51)
The photoconductors of photoconductor production examples 28 to 33 produced as described above were mounted on a single process cartridge for an image forming apparatus as shown in FIG. 5 together with a charging member (scorotron charging), and further, the full color shown in FIG. It was installed in an image forming apparatus. In the four image forming elements, a scorotron charging member is charged as a charging member under the following charging conditions, an image exposure light source is a 780 nm semiconductor laser (image writing by a polygon mirror, resolution 600 dpi), and a transfer member is transferred. Using a belt, a continuous printing of 100,000 sheets was performed using a chart with a writing rate of 6% (the test environment is 22 ° C.-55% RH).

Charging condition 1:
Discharge voltage: -6.0 kV
Grid voltage: -970V (surface potential of unexposed portion of photoconductor is -950V)
Charging condition 2:
Discharge voltage: -5.8 kV
Grid voltage: -830V (surface potential of unexposed portion of photoconductor is -800V)

The following three evaluations were performed after printing 100,000 sheets.
(I) Evaluation of soiling:
A white solid image was output, and rank evaluation was performed from the number and size of black spots generated on the background.
(Ii) Evaluation of dot formation state A 1-dot image having a diameter of 60 μm was formed, and the dot formation state was observed with a 150 × microscope.
Rank evaluation was conducted.
(Iii) Evaluation of color reproducibility After running the photoconductor and 100,000 sheets, the same full-color image was output and an attempt was made to evaluate color reproducibility.
In each case, the rank evaluation was performed in 4 stages, and very good ones were indicated by ◎, good ones by ○, slightly inferior by Δ, and very bad by x. In addition, the amount of abrasion of the photosensitive layer after printing 100,000 sheets (the amount of abrasion of the protective layer when a protective layer is provided) was measured. The above results are shown in Table 12.

  Finally, 7.3 ° which is the lowest angle peak of the Bragg angle θ, which is a feature of the titanyl phthalocyanine crystal used in the present invention, will be verified as to whether or not it is the same as the lowest angle 7.5 ° of known materials.

(Measurement Example 1)
The pigment obtained in Comparative Synthesis Example 3 (minimum angle 7.3 °) was prepared in the same manner as the pigment described in JP-A-61-239248 (having a maximum diffraction peak at 7.5 °). Weight% was added and mixed in a mortar, and the X-ray diffraction spectrum was measured in the same manner as before. The X-ray diffraction spectrum of Measurement Example 1 is shown in FIG.

(Measurement example 2)
3 was prepared in the same manner as the pigment described in JP-A-61-239248 (having a maximum diffraction peak at 7.5 °) as the pigment obtained in Comparative Synthesis Example 2 (minimum angle 7.5 °). Weight% was added and mixed in a mortar, and the X-ray diffraction spectrum was measured in the same manner as before. The X-ray diffraction spectrum of Measurement Example 2 is shown in FIG.

In the spectrum of FIG. 19, it can be seen that there are two independent peaks at 7.3 ° and 7.5 ° on the lower angle side, and at least the peaks at 7.3 ° and 7.5 ° are different. . On the other hand, in the spectrum of FIG. 18, the low angle side peak exists only at 7.5 °, which is clearly different from the spectrum of FIG.
From the above, it can be seen that the minimum angle peak of 7.3 ° in the titanyl phthalocyanine crystal of the present invention is different from the 7.5 ° peak in the known titanyl phthalocyanine crystal.

It is a figure for demonstrating the electric field strength dependence in dot formation. It is a figure for demonstrating the electric field strength dependence of a dirt rank. 1 is a schematic view for explaining an electrophotographic process and an image forming apparatus of the present invention. 1 is a schematic view for explaining a tandem-type full-color image forming apparatus of the present invention. FIG. FIG. 4 is a diagram for explaining a process cartridge for an image forming apparatus according to the present invention. It is a TEM image of amorphous titanyl phthalocyanine. The scale bar in the figure is 0.2 μm. It is a TEM image of titanyl phthalocyanine after crystal conversion. The scale bar in the figure is 0.2 μm. It is a TEM image of a titanyl phthalocyanine crystal that has undergone crystal conversion in a short time. The scale bar in the figure is 0.2 μm. It is a figure which shows the state of the dispersion liquid when dispersion time is short. It is a figure which shows the state of the dispersion liquid when dispersion time is long. It is a figure which shows an average particle diameter and a particle size distribution about the dispersion liquid of FIG. It is a figure showing the layer structure of the electrophotographic photosensitive member used for this invention. It is a figure showing the layer structure of another electrophotographic photosensitive member used for this invention. 6 is a diagram illustrating an XD spectrum of titanyl phthalocyanine synthesized in Synthesis Example 2. FIG. It is a figure showing the XD spectrum of the dry powder of the water paste. 6 is a diagram showing an XD spectrum of titanyl phthalocyanine synthesized in Comparative Synthesis Example 2. FIG. 6 is a diagram showing an XD spectrum of titanyl phthalocyanine synthesized in Comparative Synthesis Example 3. FIG. It is a figure showing the XD spectrum of the titanyl phthalocyanine used in the measurement example 1. It is a figure showing the XD spectrum of the titanyl phthalocyanine used in the measurement example 2.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Photoconductor 2 Static elimination lamp 3 Charging roller 5 Image exposure part 6 Developing unit 7 Charger before transfer 8 Registration roller 9 Transfer paper 10 Transfer charger 11 Separation charger 12 Separation claw 13 Charger before cleaning 14 Fur brush 15 Cleaning brushes 16Y, 16M, 16C , 16K photoconductors 17Y, 17M, 17C, 17K charging members 18Y, 18M, 18C, 18K laser beams 19Y, 19M, 19C, 19K developing members 20Y, 20M, 20C, 20K cleaning members 21Y, 21M, 21C, 21K transfer brush 22 Transfer conveyor belt 23 Registration roller 24 Fixing device 25Y, 25M, 25C, 25K Image forming element 26 Transfer paper 31 Conductive support 35 Charge generation layer 37 Charge transport layer 39 Protective layer 101 Photoconductor 102 Charging means 10 3 Exposure 104 Developing means 105 Transfer body 106 Transfer means 107 Cleaning means

Claims (12)

In an image forming apparatus comprising at least a scorotron charging means, an exposure means having a resolution of 600 dpi or higher, a developing means, a transfer means, and an electrophotographic photosensitive member, and operated at a photosensitive member linear velocity of 300 mm / sec or higher. The absolute value of the electric field strength applied to the electrophotographic photosensitive member from the charging means defined as follows is 30 (V / μm) or more, and the electrophotographic photosensitive member is at least on the conductive support. An electrophotographic photosensitive member in which a charge generation layer and a charge transport layer are sequentially laminated, and a diffraction peak (± 0.2 °) with a Bragg angle of 2θ with respect to a characteristic X-ray (wavelength: 1.542 mm) of CuKα in the charge generation layer. ) Having a maximum diffraction peak at least 27.2 °, further having main peaks at 9.4 °, 9.6 °, and 24.0 °, and the diffraction peak at the lowest angle side as 7. 3 Titanyl having a peak at 7.3 ° and no peak between the peak at 7.3 ° and the peak at 9.4 °, and the average size of primary particles having a peak at 26.3 ° is 0.25 μm or less A phthalocyanine crystal, the titanyl phthalocyanine crystal having a Bragg angle 2θ diffraction peak (± 0.2 °) with respect to the characteristic X-ray of CuKα (± 0.2 °) at a maximum of 7.0 to 7.5 ° Crystal transformation of amorphous titanyl phthalocyanine or low crystalline titanyl phthalocyanine having a diffraction peak and a half-width of the diffraction peak of 1 ° or more and an average primary particle size of 0.1 μm or less with an organic solvent in the presence of water The titanyl phthalocyanine after crystal conversion is separated from the organic solvent before the average primary particle size after crystal conversion grows larger than 0.3 μm. An image forming apparatus characterized in that which is filtered.
Electric field strength (V / μm) = surface potential of unexposed portion of photoreceptor at development position (V) / photosensitive layer thickness (μm)   The titanyl phthalocyanine crystal is a titanyl phthalocyanine crystal having a peak intensity of 26.3 ° in a range of 0.1 to 5% with respect to a peak intensity of a maximum diffraction peak of 27.2 °. The electrophotographic apparatus according to 1. The charge transport layer, the image forming apparatus according to claim 1 or 2, characterized in that it contains a polycarbonate containing at least triarylamine structure in its main chain and / or side chain. The image forming apparatus according to claim 1 , further comprising a protective layer on the charge transport layer. The image forming apparatus according to claim 4 , wherein the protective layer contains a metal oxide having a specific resistance of 10 ¹⁰ Ω · cm or more. The image forming apparatus according to claim 4 or 5, wherein the protective layer is characterized by containing a charge transport polymer. The image forming apparatus according to claim 4 , wherein the protective layer binder resin has a crosslinked structure. The image forming apparatus according to claim 7 , wherein a charge transporting site is included in the structure of the binder resin having the crosslinked structure. The image forming apparatus according to claim 1 , wherein the surface of the electroconductive support of the electrophotographic photosensitive member is anodized. The image forming apparatus according to claim 1 , wherein a plurality of image forming elements including at least a charging unit, an exposure unit, a developing unit, a transfer unit, and an electrophotographic photosensitive member are arranged. The image forming apparatus according to claim 1 , wherein an AC superimposed voltage is applied to the charging unit. At least charging means and the photosensitive member, exposure means, developing means, and one means selected from the cleaning means according to claim 1 to 11, characterized in that it is equipped with a universal cartridge detachable and the apparatus main body which is integral The image forming apparatus according to any one of the above.