JP5007617B2 - Organic photoreceptor and image forming apparatus - Google Patents

Description

  The present invention relates to a novel organic photoreceptor and image forming apparatus used for electrophotographic image formation used in the field of copying machines and printers.

  In recent years, there are increasing opportunities to use electrophotographic copying machines and printers in the fields of printing and color printing. In the fields of printing and color printing, there is a strong tendency to demand high-quality digital monochrome images or color images. In response to such a demand, it has been proposed to form a high-definition digital image using a short wavelength laser beam as an exposure light source. However, even if the short-wavelength laser light is used to reduce the dot diameter of the exposure and a fine electrostatic latent image is formed on the electrophotographic photosensitive member, the finally obtained electrophotographic image has sufficient high image quality. The current situation has not been achieved.

  The cause is that the photosensitive characteristics of the electrophotographic photosensitive member and the charging characteristics of the toner of the developer do not have sufficient characteristics necessary for forming a fine dot latent image or forming a toner image.

  That is, as an electrophotographic photoreceptor, an organic photoreceptor developed for a conventional long wavelength laser (hereinafter, simply referred to as a photoreceptor) has poor sensitivity characteristics, and the exposure dot diameter is reduced using a short wavelength laser beam. When the narrowed image exposure is performed, the dot latent image is not clearly formed, and the reproducibility of the dot image tends to deteriorate.

  Conventionally, anthanthrone pigments and pyranthrone compounds are well known as charge generation materials for photoreceptors for short wavelength lasers (Patent Document 1). However, the anthanthrone pigments and pyranthrone compounds described in the patent document are not described as having any special treatment, and it is considered that these pigments are simply used as commercial pigments. Sensitivity and other characteristics obtained when using commercially available pigments are not sufficient for high-speed printers and copiers using short-wavelength lasers that are expected to be developed in the future.

It is also known to perform sublimation purification to increase the sensitivity of polycyclic quinone pigments (Patent Document 2). However, the sublimation purification method described in the patent document is a simple one-time sublimation purification method, and the pigment obtained by this sublimation purification is also a high-speed printer or copying machine using a short wavelength laser. However, sufficient sensitivity and high speed are not obtained.
JP 2000-47408 A JP 57-67934 A

  The present invention has been made to solve the above problems. An object of the present invention is to form a high-density electrostatic latent image on an organic photoreceptor using image exposure such as a semiconductor laser having a oscillation wavelength of 350 to 500 nm or a light emitting diode, and to reproduce sensitivity, repeatability, or dot reproduction. It is to provide an organic photoreceptor having improved property deterioration and the like, and to provide an image forming apparatus using the organic photoreceptor.

  As a result of repeated studies on the above problems, the object of the present invention is to form a high-density electrostatic latent image on an organic photoreceptor using image exposure such as a semiconductor laser or a light emitting diode having an oscillation wavelength of 350 to 500 nm. In order to form an electrophotographic image with improved sensitivity and residual potential characteristics or dot reproducibility, a new spectral absorption characteristic with improved sensitivity characteristics for short-wavelength laser light, etc. The inventors have found that it is effective to use an organic photoreceptor having the above, and have completed the present invention.

That is, the present invention is achieved by using an organic photoreceptor having the following configuration.
1. In an organic photoreceptor having a charge generation layer and a charge transport layer on a conductive support, the charge generation layer contains a binder resin and a compound represented by the following general formula (1), and the spectrum of the charge generation layer: There has an absorption peak in each region of 400~440nm and 530～600Nm, the absorption peak intensity between the 400~440nm is rather high than the absorption peak intensity between 530～600Nm, and the following general formula (1) An organic photoreceptor, wherein the compound is a mixture of two or more compounds having different n .

(In general formula (1), n is an integer of 1 to 6)
2. Wherein 1 to charge transporting layer is characterized by containing a compound represented by the following general formula (2)
The organic photoreceptor described in 1.

(In the general formula (2), R ₁ and R ₂ each independently represent an alkyl group or an aryl group, R ₁ and R ₂ are together, may form a ring structure .R ₃ and R ₄ are each independently a hydrogen atom, an alkyl group or an aryl group, or different from each .Ar ₁ to Ar ₄ are the same Ar ₁ to Ar ₄ is representing each substituted or unsubstituted aryl group Ar ₁ and Ar ₂ , Ar ₃ and Ar ₄ may be bonded to form a ring structure, and m and n represent an integer of 1 to 4.)
3. 3. The organic photoreceptor according to 1 or 2 , a charging unit for charging the organic photoreceptor, an exposure unit for exposing the organic photoreceptor charged by the charging unit to form an electrostatic latent image, and the static a developing unit that the latent image is developed with toner to form a toner image, the toner image and a transfer means for transferring to a transfer medium from said organic photoreceptor, in the main scanning direction of the writing in the exposing unit An image forming apparatus having an exposure diameter of 10 to 50 μm.
4). 3. The organic photoreceptor according to 1 or 2 , a charging unit for charging the organic photoreceptor, an exposure unit for exposing the organic photoreceptor charged by the charging unit to form an electrostatic latent image, and the static A developing unit that develops the electrostatic latent image with toner to form a toner image; and a transfer unit that transfers the toner image from the organic photoreceptor to a transfer medium. The exposure unit has a wavelength range of 350 to 500 nm. An image forming apparatus comprising the monochromatic light as an exposure light source.
5. 3. The organic photoreceptor according to 1 or 2 , a charging unit for charging the organic photoreceptor, an exposure unit for exposing the organic photoreceptor charged by the charging unit to form an electrostatic latent image, and the static A developing unit that develops the electrostatic latent image with toner to form a toner image; and a transfer unit that transfers the toner image from the organic photoreceptor to a transfer medium. The exposure unit includes three or more vertical and horizontal exposure units. A multi-beam method in which a surface emitting laser array having a laser beam emission point in a wavelength range of 350 to 500 nm is provided as an exposure light source, and the laser beam emission point is scanned on the organic photoreceptor to form the electrostatic latent image. An image forming apparatus, comprising:
6). 6. The image forming apparatus according to any one of 3 to 5, wherein a writing density is 1200 dpi or more.

  By using the organophotoreceptor and the image forming apparatus of the present invention, in an electrophotographic image forming system using a short wavelength laser beam or the like, the potential attenuation value with respect to the unit exposure amount is large, the repetition characteristic is also good, and the small diameter dot A latent image can be formed sharply, and an electrophotographic image with improved dot reproducibility can be formed.

  Hereinafter, the organic photoreceptor of the present invention will be described in detail.

  The organic photoreceptor of the present invention is an organic photoreceptor having a charge generation layer and a charge transport layer on a conductive support, wherein the charge generation layer contains a binder resin and a compound represented by the following general formula (1), And the spectral spectrum of the charge generation layer has an absorption peak in each region of 400 to 440 nm and 530 to 600 nm, and the absorption peak intensity between 400 to 440 nm is higher than the absorption peak intensity between 530 to 600 nm. And

  The organophotoreceptor of the present invention has the above-described configuration, so that a high-definition dot image can be formed in an electrophotographic image forming system using a short wavelength laser beam or the like, and the potential attenuation with respect to the unit exposure amount. It has a large value and good repeatability, can form a small dot latent image sharply, and can form an electrophotographic image with improved dot reproducibility.

  Hereinafter, the organic photoreceptor of the present invention will be described in detail.

  First, the spectrum of the charge generation layer according to the present invention will be described.

  The spectrum of the charge generation layer according to the present invention has an absorption peak in each region of 400 to 440 nm and 530 to 600 nm, and the absorption peak intensity between 400 to 440 nm is higher than the absorption peak intensity between 530 to 600 nm. It is characterized by that.

  The spectrum of the charge generation layer was measured with an ultraviolet-visible spectrophotometer V-530 (manufactured by JASCO Corporation) after forming the charge generation layer on a transparent polyester film with the same film thickness as the photoreceptor. (Scanning speed 1000 nm / min).

  The absorption peak can be directly read from the spectral spectrum graph of the spectral spectrum, but when it is difficult to identify the peak, it can be identified by drawing a differential curve of the spectral spectrum graph.

  Further, when a plurality of absorption peaks exist in each region of 400 to 440 nm and 530 to 600 nm, the intensity comparison is performed with the maximum absorption peak of each region.

  Since the organophotoreceptor of the present invention has the spectral spectral characteristics as described above, the present invention has a large potential attenuation value with respect to the unit exposure amount with respect to image exposure by monochromatic light such as laser light in the wavelength region of 380 to 500 nm. In addition, the repetition characteristics are also good, a small-diameter dot latent image can be formed sharply, and an electrophotographic image with improved dot reproducibility can be formed.

  The reason for the effect of the present invention has not been sufficiently elucidated, but in addition to the monomer absorption property on the short wavelength side of the compound of the general formula (1), the absorption property due to the aggregate on the long wavelength side It is thought that this is derived from the fact that the photoexcited counter-electron can be sustained for a long time by developing a high level of.

  Next, the compound of the general formula (1) according to the present invention will be described.

In the compound of the general formula (1), the number of substituted Br and n is 1 to 6, and the substitution positions of these Br can be substituted at the positions of R _{1 to} R _{14 in} the following general formula (3).

  However, a means for accurately specifying the substitution position of Br has not been established, and the substitution position cannot be accurately specified.

  Further, as shown in the following synthesis example, the compound of the general formula (1) is obtained as a mixture having a plurality of substituted Br and n, and these mixtures are used as a charge generating material for the charge generation layer. Is preferred.

  Below, the synthesis example of the compound represented by the said General formula (1) concerning this invention is described.

Synthesis example 1
CGM-1 (mixture of n = 1 to 3)
8,16-pyrans range on: 5.0 g, iodine: 0.25 g was dissolved in chlorosulfuric acid: 50 g, and 3.0 g of bromine was added dropwise. The mixture was heated and stirred at 50 ° C. for 3 hours, cooled to room temperature, and then poured into 500 g of ice. Filtration, washing with water and drying yielded 6.8 g of a crude pigment product. 5.0 g of crude pigment is placed in a Pyrex glass tube, and the tube is heated to a temperature gradient of about 440 ° C. to about 20 ° C. along the length of the tube (1 meter length, about 440 ° C. to about 20 ° C.). (With a temperature gradient of 0 ° C.) was placed inside the furnace. The inside of the glass tube was depressurized to about 133.3 Pa to 13.3 Pa, and the position where the crude pigment to be purified was placed was heated to about 440 ° C. The generated vapor was transferred to the low temperature side of the tube and condensed to obtain 2.4 g of sublimate (CGM-1) condensed in a region between about 300 to 380 ° C.

  As a result of measuring the mass spectrum of CGM-1, it was a mixture of n = 1 to 3, and the peak intensity ratio of n = 1 / n = 2 / n = 3 was 11/59/30.

Synthesis example 2
CGM-2 (mixture of n = 3-5)
8,16-pyrans range-on: 5.0 g, iodine: 0.25 g was dissolved in chlorosulfuric acid: 50 g, and 5.9 g of bromine was added dropwise. The mixture was heated and stirred at 70 ° C. for 5 hours, cooled to room temperature, and then poured into 500 g of ice. Filtration, washing with water and drying yielded 8.5 g of a crude pigment product. 5.0 g of crude pigment is placed in a Pyrex glass tube, and the tube is subjected to a temperature gradient of about 460 ° C. to about 20 ° C. along the length of the tube (1 m long, about 460 ° C. to about 20 ° C.). (With a temperature gradient of 0 ° C.) was placed inside the furnace. The inside of the glass tube was depressurized to about 133.3 Pa to 13.3 Pa, and the position where the crude pigment to be purified was placed was heated to about 460 ° C. The generated vapor was transferred to the low temperature side of the tube and condensed to obtain 3.3 g of a sublimate condensed in a region between about 300 to 400 ° C.

  As a result of mass spectrum measurement, it was a mixture of n = 3 to 5, and the peak intensity ratio of n = 3 / n = 4 / n = 5 was 16/67/17.

Synthesis example 3
CGM-3 (mixture of n = 3-6)
8,16-pyrans range-on: 5.0 g, iodine: 0.25 g was dissolved in chlorosulfuric acid: 50 g, and 5.9 g of bromine was added dropwise. The mixture was heated and stirred at 75 ° C. for 6 hours, cooled to room temperature, and then poured into 500 g of ice. After filtration, washing with water and drying, 8.7 g of a crude pigment product was obtained. 5.0 g of crude pigment is placed in a Pyrex glass tube, and the tube is subjected to a temperature gradient of about 480 ° C. to about 20 ° C. along the length of the tube (1 m long, about 480 ° C. to about 20 ° C.). (With a temperature gradient of 0 ° C.) was placed inside the furnace. The inside of the glass tube was depressurized to about 133.3 Pa to 13.3 Pa, and the position where the crude pigment to be purified was placed was heated to about 480 ° C. The generated vapor was moved to the low temperature side of the tube and condensed to obtain 3.0 g of sublimate (CGM-2)) condensed in a region between about 300 to 420 ° C.

  As a result of mass spectrum measurement of CGM-3, it was a mixture of n = 3 to 6, and the peak intensity ratio of n = 3 / n = 4 / n = 5 / n = 6 was 17/51/27/5. .

  The charge generation layer according to the present invention requires a binder. If the binder is not present, good effects cannot be obtained even if the spectral absorption spectrum is within the present invention.

  Moreover, it is preferable to refine | purify the compound of the said General formula (1) concerning this invention by performing advanced sublimation purification. Here, advanced sublimation purification refers to multi-stage sublimation purification and fractional sublimation purification as described below, and it is difficult to obtain the aforementioned spectral absorption spectrum characteristics by simple one-stage sublimation purification.

a. Multi-stage sublimation purification Multi-stage sublimation purification includes two or more sublimation steps. The first stage condenses an effective amount, for example about 1-10% by weight of the sublimate, onto the first substrate at a temperature slightly above the sublimation temperature of the pigment. Subsequently, in the second stage, the sublimation temperature is raised in the range of 10 to 100 ° C., and the sublimate is condensed on the second substrate, whereby a high-purity pigment containing no volatile impurities or decomposition impurities can be obtained. Depending on the case, three or more steps may be included.

b. Fractional Sublimation Purification Fractional sublimation purification means that the pigment is first heated to the temperature T1 at the first position to evaporate the pigment and volatile impurities contained therein, and then the pigment is maintained at the second position where the temperature T2 is lower than T1. This is done by condensing the vapor and subsequently condensing the vapor of volatile impurities at a third position maintained at a temperature T3 lower than T2. Non-sublimable impurities remain in the first position with the starting material, and a purified pigment separated from volatile impurities is obtained. The fractional sublimation method of the present invention includes a known purification method such as train sublimation using a glass tube.

  Next, the charge transport material of the general formula (2) according to the present invention will be described.

  Specific compound examples of the general formula (2) are shown below.

  Synthesis Example 1 (CTM-6)

A 200ml 4-head Kolben is equipped with a cooling tube, thermometer and nitrogen inlet tube, and a magnetic stirrer is set. The system is depressurized and completely purged with nitrogen. To this Kolben, (a) 8.1 g, (b) 12.0 g, K ₂ CO ₃ 16 g, Cu powder 8.0 g, and nitrobenzene 40 ml were sequentially added and stirred at 190 ° C. for 30 hours. Reacted. Then, after processing the said reaction liquid by steam distillation, this was isolate | separated and refined by column chromatography using the developing solvent of hexane / toluene (4/1), and 12g of target CTM-6 was obtained. Confirmation of the target product could be confirmed by mass spectrometry and NMR.

  The organic photoreceptor according to the present invention is an organic photoreceptor having a charge generation layer and a charge transport layer on a conductive support, and the charge generation layer contains a binder resin and a compound represented by the general formula (1). And the spectrum of the charge generation layer has an absorption peak in each region of 400 to 440 nm and 530 to 600 nm, and the absorption peak intensity between 400 to 440 nm is higher than the absorption peak intensity between 530 to 600 nm. The structure of the organic photoreceptor having these structures is described below.

  In the present invention, the organic photoconductor means an electrophotographic photoconductor constituted by providing an organic compound with at least one of a charge generation function and a charge transport function essential to the configuration of the electrophotographic photoconductor. All known organic photoconductors such as a photoconductor composed of an organic charge generating material or an organic charge transport material, a photoconductor composed of a polymer complex with a charge generating function and a charge transport function are contained.

Examples of the layer structure of the organophotoreceptor of the present invention include the following layer structures;
1) A structure in which a charge generation layer and a charge transport layer are sequentially laminated as a photosensitive layer on a conductive support;
2) A structure in which a charge generation layer, a first charge transport layer, and a second charge transport layer are sequentially laminated as a photosensitive layer on a conductive support;
3) A structure in which a surface protective layer is further formed on the photosensitive layer of the photoreceptor of 1) or 2) above.

  The photoconductor may have any of the above configurations. In addition, the photoreceptor of the present invention may have any configuration, and an undercoat layer (intermediate layer) may be formed on the conductive support prior to the formation of the photosensitive layer.

  The charge transport layer means a layer having a function of transporting charge carriers generated in the charge generation layer by photoexposure to the surface of the organic photoreceptor, and the specific detection of the charge transport function is carried out between the charge generation layer and the charge transport layer. It can be confirmed by laminating a transport layer on a conductive support and detecting optical conductivity.

  Next, the layer structure of the organic photoreceptor will be described focusing on the structure of 1) above.

Conductive Support The conductive support used for the photoreceptor may be either a sheet or a cylinder, but a cylindrical conductive support is preferred for designing an image forming apparatus compactly. .

  Cylindrical conductive support means a cylindrical support necessary for forming an endless image by rotating. Conductivity is within a range of 0.1 mm or less in straightness and 0.1 mm or less in deflection. A support is preferred. Exceeding the range of straightness and shake makes it difficult to form a good image.

As the conductive material, a metal drum such as aluminum or nickel, a plastic drum deposited with aluminum, tin oxide, indium oxide, or the like, or a paper or plastic drum coated with a conductive substance can be used. The conductive support preferably has a specific resistance of 10 ³ Ωcm or less at room temperature. The conductive support of the present invention is most preferably an aluminum support. As the aluminum support, one in which components such as manganese, zinc, magnesium and the like are mixed in addition to the main component aluminum is also used.

Intermediate layer In the present invention, an intermediate layer is preferably provided between the conductive support and the photosensitive layer.

  The intermediate layer used in the present invention preferably contains N-type semiconductor particles. The N-type semiconductive particle means a particle whose main charge carrier is an electron. That is, since the main charge carriers are electrons, the intermediate layer containing the N-type semiconductive particles in the insulating binder effectively blocks hole injection from the substrate, and the electrons from the photosensitive layer. In contrast, it has a property of low blocking.

As the N-type semiconductor particles, titanium oxide (TiO ₂ ) and zinc oxide (ZnO) are preferable, and titanium oxide is particularly preferably used.

  As the N-type semiconductor particles, fine particles having a number average primary particle size in the range of 3.0 to 200 nm are used. Particularly, 5 nm to 100 nm is preferable. The number average primary particle diameter is a measured value as an average diameter in the ferret direction by observing 100 particles as primary particles at random by magnifying the fine particles 10,000 times by transmission electron microscope observation and image analysis. N-type semiconducting particles having a number average primary particle size of less than 3.0 nm are difficult to uniformly disperse in the intermediate layer binder, and easily form aggregated particles. Is likely to occur. On the other hand, N-type semiconducting particles having a number average primary particle size larger than 200 nm tend to make large irregularities on the surface of the intermediate layer, and the dot image tends to deteriorate through these large irregularities. In addition, the N-type semiconductive particles having a number average primary particle size larger than 200 nm are likely to precipitate in the dispersion and easily generate aggregates. As a result, the dot image tends to deteriorate.

  The titanium oxide particles have anatase, rutile, brookite, and amorphous forms as crystal forms. Among them, the rutile form titanium oxide pigment or the anatase form titanium oxide pigment has a rectifying property of charge passing through the intermediate layer. In other words, the mobility of electrons is increased, the charging potential is stabilized, the residual potential is prevented from increasing, and the dot image is prevented from deteriorating, which is most preferable as the N-type semiconductor particles of the present invention. .

  N-type semiconductive particles are preferably surface-treated with a polymer containing methylhydrogensiloxane units. The molecular weight of the polymer containing the methyl hydrogen siloxane unit is 1000 to 20000, and the surface treatment effect is high. As a result, the rectifying property of the N-type semiconductor particles is improved, and the N-type semiconductor particles are contained. By using the intermediate layer, the occurrence of black spots is prevented and there is an effect on the reproducibility of good dot images.

The polymer containing a methylhydrogensiloxane unit is preferably a copolymer of a structural unit of-(HSi (CH ₃ ) O)-and a structural unit other than this (other siloxane unit). As other siloxane units, dimethylsiloxane units, methylethylsiloxane units, methylphenylsiloxane units, diethylsiloxane units, and the like are preferable, and dimethylsiloxane is particularly preferable. The proportion of methylhydrogensiloxane units in the copolymer is 10 to 99 mol%, preferably 20 to 90 mol%.

  The methylhydrogensiloxane copolymer may be any of a random copolymer, a block copolymer, a graft copolymer, etc., but a random copolymer and a block copolymer are preferred. In addition to methylhydrogensiloxane, the copolymerization component may be one component or two or more components.

  The intermediate layer coating solution prepared for forming the intermediate layer used in the present invention is composed of a binder resin, a dispersion solvent and the like in addition to the N-type semiconductive particles such as the surface-treated titanium oxide.

  The ratio of the N-type semiconductive particles in the intermediate layer is preferably 1.0 to 2.0 times in terms of the volume ratio of the intermediate layer to the binder resin (when the volume of the binder resin is 1). By using the N-type semiconducting particles of the present invention at such a high density in the intermediate layer, the rectification of the intermediate layer is enhanced, and the increase in residual potential and dot image degradation are effective even when the film thickness is increased. Therefore, a good organic photoreceptor can be formed. Further, such an intermediate layer preferably uses 100 to 200 parts by volume of N-type semiconductive particles with respect to 100 parts by volume of the binder resin.

  On the other hand, the binder resin in which these particles are dispersed to form the layer structure of the intermediate layer is preferably a polyamide resin in order to obtain good dispersibility of the particles, but the polyamide resin shown below is particularly preferable.

  The binder resin for the intermediate layer is preferably an alcohol-soluble polyamide resin. As the binder resin for the intermediate layer of the organic photoreceptor, a resin having excellent solvent solubility is required in order to form the intermediate layer with a uniform film thickness. As such alcohol-soluble polyamide resins, copolymerized polyamide resins and methoxymethylated polyamide resins composed of a chemical structure with few carbon chains between amide bonds such as 6-nylon described above are known. Surprisingly, polyamides having the following components can also be preferably used.

  The component ratio in the polyamides N-1 to N-5 is expressed in mol%.

  The molecular weight of the polyamide resin is preferably 5,000 to 80,000 in terms of number average molecular weight, and more preferably 10,000 to 60,000. When the number average molecular weight is 5,000 or less, the uniformity of the film thickness of the intermediate layer is deteriorated, and the effects of the present invention are not sufficiently exhibited. On the other hand, if it is larger than 80,000, the solvent solubility of the resin is likely to be reduced, and an agglomerated resin is likely to be generated in the intermediate layer, which tends to cause black spots and deterioration of the dot image.

  A part of the polyamide resin is already available on the market. For example, the polyamide resin is sold under the trade names such as Vestamelt X1010 and X4685 manufactured by Daicel-Degussa Co., Ltd., and can be prepared by a general polyamide synthesis method. An example of synthesis is given below.

  As the solvent for dissolving the polyamide resin and preparing the coating solution, alcohols having 2 to 4 carbon atoms such as ethanol, n-propyl alcohol, isopropyl alcohol, n-butanol, t-butanol, sec-butanol are preferable, It is excellent in the solubility of polyamide and the coating property of the prepared coating solution. These solvents are 30 to 100% by mass, preferably 40 to 100% by mass, and more preferably 50 to 100% by mass in the total solvent. Examples of co-solvents that can be used in combination with the above-mentioned solvent to obtain preferable effects include methanol, benzyl alcohol, toluene, methylene chloride, cyclohexanone, and tetrahydrofuran.

  The thickness of the intermediate layer of the present invention is preferably 0.3 to 10 μm. If the thickness of the intermediate layer is less than 0.5 μm, black spots or the like are likely to occur, and the dot image is likely to deteriorate. If it exceeds 10 μm, the residual potential is likely to increase, and the dot image tends to deteriorate. As for the film thickness of an intermediate | middle layer, 0.5-5 micrometers is more preferable.

Moreover, it is preferable that the said intermediate | middle layer is an insulating layer substantially. Here, the insulating layer has a volume resistance of 1 × 10 ⁸ Ω · cm or more. The volume resistance of the intermediate layer and the protective layer of the present invention is preferably 1 × 10 ⁸ to 10 ¹⁵ Ω · cm, more preferably 1 × 10 ⁹ to 10 ¹⁴ Ω · cm, and further preferably 2 × 10 ⁹ to 1 ×. 10 ¹³ Ω · cm. The volume resistance can be measured as follows.

  Measurement conditions: According to JIS: C2318-1975.

Measuring instrument: Hiresta IP manufactured by Mitsubishi Yuka
Measurement conditions: Measurement probe HRS
Applied voltage: 500V
Measurement environment: 30 ± 2 ℃, 80 ± 5RH%
When the volume resistance is less than 1 × 10 ⁸ Ω · cm, the charge blocking property of the intermediate layer decreases, the occurrence of black spots increases, the potential holding property of the organic photoreceptor deteriorates, and good image quality cannot be obtained. On the other hand, if it is greater than 10 ¹⁵ Ω · cm, the residual potential tends to increase in repeated image formation, and good image quality cannot be obtained.

Photosensitive layer The photosensitive layer configuration of the photoreceptor of the present invention may be a single-layer photosensitive layer configuration in which the intermediate layer has a charge generation function and a charge transport function in one layer, but more preferably the function of the photosensitive layer. The charge generation layer (CGL) and the charge transport layer (CTL) may be separated from each other. By adopting a configuration in which the functions are separated, an increase in the residual potential due to repeated use can be controlled to be small, and other electrophotographic characteristics can be easily controlled according to the purpose. In the negatively charged photoconductor, it is preferable that a charge generation layer (CGL) is formed on the intermediate layer, and a charge transport layer (CTL) is formed thereon.

  The structure of the photosensitive layer of the function-separated negatively charged photoreceptor will be described below.

Charge Generation Layer The organic photoreceptor of the present invention contains the compound represented by the general formula (1) as a charge generation material. In addition to this charge generation material, other charge generation materials may be used in combination as required. Examples of the pigment used in combination include azo pigments, perylene pigments, and multisensitive quinone pigments.

  The charge generation layer requires a binder as a CGM dispersion medium. As the binder, known resins can be used, and the most preferred resins include formal resin, butyral resin, silicone resin, silicone-modified butyral resin, phenoxy resin and the like. The ratio of the binder resin to the charge generating material is preferably 20 to 600 parts by mass with respect to 100 parts by mass of the binder resin. By using these resins, the increase in residual potential associated with repeated use can be minimized. The thickness of the charge generation layer is preferably 0.3 μm to 2 μm.

Charge Transport Layer In the present invention, the charge transport layer may be composed of a plurality of charge transport layers, and the uppermost charge transport layer may contain the inorganic fine particles of the present invention.

  The charge transport layer contains a charge transport material (CTM) and a binder resin that disperses and forms a CTM. As other substances, additives such as an antioxidant may be contained in addition to the inorganic fine particles as necessary.

  As the charge transport material (CTM), a known hole transport property (P-type) charge transport material (CTM) can be used. For example, a triphenylamine derivative, a hydrazone compound, a styryl compound, a benzidine compound, a butadiene compound, or the like can be used. Among these, the charge transport material of the general formula (2) that does not absorb in the wavelength region of 400 to 500 nm is preferable.

  These charge transport materials are usually dissolved in a suitable binder resin to form a layer. The binder resin used for the charge transport layer (CTL) may be either a thermoplastic resin or a thermosetting resin. For example, polystyrene, acrylic resin, methacrylic resin, vinyl chloride resin, vinyl acetate resin, polyvinyl butyral resin, epoxy resin, polyurethane resin, phenol resin, polyester resin, alkyd resin, polycarbonate resin, silicone resin, melamine resin, and these resins A copolymer resin containing two or more of the repeating unit structures. In addition to these insulating resins, high molecular organic semiconductors such as poly-N-vinylcarbazole can be used. Of these, polycarbonate resins are most preferred because of their low water absorption and good CTM dispersibility and electrophotographic characteristics.

  The ratio of the binder resin to the charge transport material is preferably 50 to 200 parts by mass with respect to 100 parts by mass of the binder resin.

  The total film thickness of the charge transport layer is preferably 10 to 30 μm. If the total film thickness is less than 10 μm, it is difficult to sufficiently obtain the latent image potential during development, and the image density and the dot reproducibility are liable to be deteriorated. Diffusion of charge carriers generated in the generation layer) increases, and dot reproducibility tends to deteriorate. Further, when the charge transport layer is formed of a plurality of layers, the thickness of the charge transport layer serving as the surface layer is preferably 1.0 to 8.0 μm.

  Solvents or dispersion media used to form layers such as intermediate layers, charge generation layers, and charge transport layers include n-butylamine, diethylamine, ethylenediamine, isopropanolamine, triethanolamine, triethylenediamine, N, N-dimethylformamide, acetone , Methyl ethyl ketone, methyl isopropyl ketone, cyclohexanone, benzene, toluene, xylene, chloroform, dichloromethane, 1,2-dichloroethane, 1,2-dichloropropane, 1,1,2-trichloroethane, 1,1,1-trichloroethane, trichloroethylene, Tetrachloroethane, tetrahydrofuran, dioxolane, dioxane, methanol, ethanol, butanol, isopropanol, ethyl acetate, butyl acetate, dimethyl sulfoxide, methyl cello Lube, and the like. Although this invention is not limited to these, Solvents friendly to global environment, such as tetrahydrofuran and methyl ethyl ketone, are used preferably. These solvents may be used alone or as a mixed solvent of two or more.

  Next, as a coating processing method for producing the organic photoreceptor, a coating processing method such as dip coating or spray coating is used in addition to the slide hopper type coating device.

  Among the above coating liquid supply type coating apparatuses, the coating method using a slide hopper type coating apparatus is most suitable when the above-described dispersion using a low boiling point solvent is used as the coating liquid, and is a cylindrical photoconductor. In this case, the coating is preferably performed using a circular slide hopper type coating apparatus described in detail in JP-A No. 58-189061 and the like.

  The surface layer of the photoreceptor according to the present invention preferably contains an antioxidant. The surface layer is easily oxidized by an active gas such as NOx or ozone during charging of the photoconductor, and image blur is likely to occur. However, the presence of an antioxidant can prevent image blur. Typical examples of the antioxidants are those that prevent the action of oxygen under conditions of light, heat, discharge, etc. on auto-oxidizing substances present in the organic photoreceptor or on the surface of the organic photoreceptor, It is a substance that has the property of inhibiting.

  Solvents or dispersion media used to form layers such as intermediate layers, charge generation layers, and charge transport layers include n-butylamine, diethylamine, ethylenediamine, isopropanolamine, triethanolamine, triethylenediamine, N, N-dimethylformamide, acetone , Methyl ethyl ketone, methyl isopropyl ketone, cyclohexanone, benzene, toluene, xylene, chloroform, dichloromethane, 1,2-dichloroethane, 1,2-dichloropropane, 1,1,2-trichloroethane, 1,1,1-trichloroethane, trichloroethylene, Tetrachloroethane, tetrahydrofuran, dioxolane, dioxane, methanol, ethanol, butanol, isopropanol, ethyl acetate, butyl acetate, dimethyl sulfoxide, methyl cello Lube, and the like. Although this invention is not limited to these, Dichloromethane, 1, 2- dichloroethane, methyl ethyl ketone, etc. are used preferably. These solvents may be used alone or as a mixed solvent of two or more.

  Next, an image forming apparatus using the organic photoreceptor according to the present invention will be described.

  An image forming apparatus 1 shown in FIG. 1 is a digital image forming apparatus, and includes an image reading unit A, an image processing unit B, an image forming unit C, and a transfer paper transport unit D as a transfer paper transport unit. Yes.

  An automatic document feeder that automatically conveys the document is provided above the image reading unit A. The document placed on the document table 11 is separated and conveyed by the document conveyance roller 12 to the reading position 13a. The image is read. The document after the document reading is completed is discharged onto the document discharge tray 14 by the document transport roller 12.

  On the other hand, the image of the original when placed on the platen glass 13 is read at a speed v of the first mirror unit 15 including the illumination lamp and the first mirror constituting the scanning optical system, and the V-shaped first image is located. Reading is performed by the movement of the second mirror unit 16 including the two mirrors and the third mirror in the same direction at the speed v / 2.

  The read image is formed on the light receiving surface of the image sensor CCD, which is a line sensor, through the projection lens 17. The line-shaped optical image formed on the image sensor CCD is sequentially photoelectrically converted into an electric signal (luminance signal) and then A / D converted, and the image processing unit B performs processing such as density conversion and filter processing. Then, the image data is temporarily stored in the memory.

  In the image forming unit C, as an image forming unit, a drum-shaped photoconductor 21 as an image carrier, a charging means (charging step) 22 for charging the photoconductor 21 on the outer periphery thereof, and a surface potential of the charged photoconductor. Potential detecting means 220 for detecting the toner, developing means (developing process) 23, transfer conveying belt device 45 as a transferring means (transfer process), cleaning device (cleaning process) 26 for the photosensitive member 21, and light neutralizing means (light slow charge). PCL (precharge lamp) 27 as a process is arranged in the order of operation. Further, on the downstream side of the developing means 23, a reflection density detecting means 222 for measuring the reflection density of the patch image developed on the photosensitive member 21 is provided. As the photosensitive member 21, the organic photosensitive member according to the present invention is used, and the photosensitive member 21 is driven and rotated in the clockwise direction shown in the drawing.

  After the rotating photosensitive member 21 is uniformly charged by the charging unit 22, an image based on an image signal called from the memory of the image processing unit B by an exposure optical system as an image exposure unit (image exposure step) 30 is used. Exposure is performed. The exposure optical system as the image exposure means 30 as the writing means uses a laser diode (not shown) as a light source, and the optical path is bent by the reflection mirror 32 via the rotating polygon mirror 31, the fθ lens 34, and the cylindrical lens 35, and main scanning is performed. Therefore, image exposure is performed on the photoconductor 21 at the position Ao, and an electrostatic latent image is formed by rotation (sub-scanning) of the photoconductor 21. In one example of the present embodiment, the character portion is exposed to form an electrostatic latent image.

In the image forming apparatus of the present invention, a semiconductor laser or a light emitting diode having an oscillation wavelength of 350 to 500 nm is used as an image exposure light source when an electrostatic latent image is formed on a photoreceptor. By using these image exposure light sources, the exposure dot diameter in the main scanning direction of writing is narrowed down to 10 to 50 μm, and digital exposure is performed on the organic photoreceptor, so that it is 600 dpi (dpi: the number of dots per 2.54 cm) or more. To high resolution electrophotographic images of 2500 dpi can be obtained.

  As the image exposure light source of the semiconductor laser, a surface emitting laser array can also be used. As shown in FIG. 4, the surface emitting laser array means one having at least three laser beam emission points (L) in each of the vertical and horizontal directions.

The exposure dot diameter refers to the length of the exposure beam (Ld: measured at the maximum position) along the main scanning direction in a region where the intensity of the exposure beam is 1 / e ² or more of the peak intensity.

The light beams used have a solid scanner such as the scanning optical system and LED using a semiconductor laser, there is a Gaussian distribution and Lorentz distribution, etc. also the light intensity distribution is in each 1 / e ² or more regions of peak intensity The exposure dot diameter according to the present invention is used.

  The electrostatic latent image on the photoconductor 21 is reversely developed by the developing unit 23, and a visible toner image is formed on the surface of the photoconductor 21. In the image forming method of the present invention, it is preferable to use a polymerized toner as a developer used in the developing means. By using a polymer toner having a uniform shape and particle size distribution in combination with the organic photoreceptor according to the present invention, an electrophotographic image with better sharpness can be obtained.

  The electrostatic latent image formed on the organic photoreceptor of the present invention is visualized as a toner image by development. The toner used for development may be a pulverized toner or a polymerized toner, but the toner according to the present invention is preferably a polymerized toner that can be prepared by a polymerization method from the viewpoint of obtaining a stable particle size distribution.

  The term “polymerized toner” means a toner in which a toner binder resin is formed and the toner shape is formed by polymerization of a raw material monomer of the binder resin and, if necessary, subsequent chemical treatment. More specifically, it means a toner formed through a polymerization reaction such as suspension polymerization or emulsion polymerization, and if necessary, a step of fusing particles between them.

  The volume average particle diameter of the toner, that is, the 50% volume particle diameter (Dv50) is preferably 2 to 9 μm, more preferably 3 to 7 μm. By setting this range, the resolution can be increased. In addition, by combining with the above range, the amount of toner having a fine particle diameter can be reduced while being a small particle diameter toner, the dot image reproducibility is improved over a long period of time, and the sharpness is excellent. In addition, a stable image can be formed.

  The toner according to the present invention may be used as a one-component developer or a two-component developer.

  When used as a one-component developer, a non-magnetic one-component developer or a magnetic one-component developer containing about 0.1 to 0.5 μm of magnetic particles in the toner can be used. be able to.

  Further, it can be mixed with a carrier and used as a two-component developer. In this case, conventionally known materials such as metals such as iron, ferrite and magnetite, and alloys of these metals with metals such as aluminum and lead can be used as the magnetic particles of the carrier. Ferrite particles are particularly preferable. The magnetic particles preferably have a volume average particle size of 15 to 100 μm, more preferably 25 to 80 μm.

  The volume average particle diameter of the carrier can be typically measured by a laser diffraction particle size distribution measuring apparatus “HELOS” (manufactured by SYMPATEC) equipped with a wet disperser.

  The carrier is preferably a carrier in which magnetic particles are further coated with a resin, or a so-called resin dispersion type carrier in which magnetic particles are dispersed in a resin. The resin composition for coating is not particularly limited, and for example, olefin resin, styrene resin, styrene-acrylic resin, silicone resin, ester resin, or fluorine-containing polymer resin is used. In addition, the resin for constituting the resin-dispersed carrier is not particularly limited, and a known resin can be used. For example, a styrene-acrylic resin, a polyester resin, a fluorine resin, a phenol resin, or the like is used. be able to.

  In the transfer paper transport section D, paper feed units 41 (A), 41 (B), and 41 (C) are provided below the image forming unit as transfer paper storage means for storing transfer paper P of different sizes. Further, a manual paper feeding unit 42 for manually feeding paper is provided on the side, and the transfer paper P selected from any of them is fed along the transport path 40 by the guide roller 43 and fed. The transfer paper P is temporarily stopped by a pair of paper feed registration rollers 44 that correct the inclination and bias of the transfer paper P to be transferred, and then fed again. The transport path 40, the pre-transfer roller 43a, and the paper feed path 46 The toner image on the photosensitive member 21 is transferred to the transfer paper P while being transferred to the transfer conveyance belt 454 of the transfer conveyance belt device 45 by the transfer electrode 24 and the separation electrode 25 at the transfer position Bo. Is, transfer sheet P is separated from the photosensitive member 21 surface, it is conveyed to the fixing unit 50 by the transfer conveyor belt device 45.

  The fixing unit 50 includes a fixing roller 51 and a pressure roller 52. By passing the transfer paper P between the fixing roller 51 and the pressure roller 52, the toner is fixed by heating and pressing. After the toner image has been fixed, the transfer paper P is discharged onto the paper discharge tray 64.

  The above describes the state in which image formation is performed on one side of the transfer paper. However, in the case of double-sided copying, the paper discharge switching member 170 is switched, the transfer paper guide 177 is opened, and the transfer paper P is indicated by a broken arrow. Conveyed in the direction.

  Further, the transfer paper P is transported downward by the transport mechanism 178 and switched back by the transfer paper reversing unit 179, and the rear end portion of the transfer paper P becomes the leading end portion and transported into the duplex copying paper supply unit 130. The

  The transfer paper P is moved in a paper feed direction by a conveyance guide 131 provided in the double-sided copy paper supply unit 130, the transfer paper P is re-fed by the paper supply roller 132, and the transfer paper P is guided to the conveyance path 40. .

  Again, as described above, the transfer paper P is conveyed in the direction of the photosensitive member 21, the toner image is transferred to the back surface of the transfer paper P, fixed by the fixing unit 50, and then discharged onto the paper discharge tray 64.

  The image forming apparatus of the present invention is configured by integrally combining the above-described photosensitive member and components such as a developing device and a cleaning device as a process cartridge, and this unit is configured to be detachable from the apparatus main body. Also good. In addition, a process cartridge is formed by integrally supporting at least one of a charger, an image exposure device, a developing device, a transfer or separation device, and a cleaning device together with a photosensitive member, and a single unit that is detachable from the apparatus main body. It is good also as a structure which can be attached or detached using guide means, such as a rail of an apparatus main body.

  FIG. 2 is a cross-sectional configuration diagram of a color image forming apparatus showing an embodiment of the present invention.

  This color image forming apparatus is called a tandem type color image forming apparatus, and includes four sets of image forming units (image forming units) 10Y, 10M, 10C, and 10Bk, an endless belt-shaped intermediate transfer body unit 7, and a feeding unit. It comprises a paper conveying means 21 and a fixing means 24. A document image reading device SC is disposed on the upper part of the main body A of the image forming apparatus.

  The image forming unit 10Y that forms a yellow image includes a charging unit (charging step) 2Y, an exposure unit (exposure step) 3Y, and a developing unit disposed around a drum-shaped photoconductor 1Y as a first image carrier. A unit (developing step) 4Y, a primary transfer roller 5Y as a primary transfer unit (primary transfer step), and a cleaning unit 6Y. An image forming unit 10M that forms a magenta image includes a drum-shaped photosensitive member 1M as a first image carrier, a charging unit 2M, an exposure unit 3M, a developing unit 4M, a primary transfer roller 5M as a primary transfer unit, It has a cleaning means 6M. An image forming unit 10C for forming a cyan image includes a drum-shaped photoreceptor 1C as a first image carrier, a charging unit 2C, an exposure unit 3C, a developing unit 4C, and a primary transfer roller 5C as a primary transfer unit. It has cleaning means 6C. The image forming unit 10Bk that forms a black image includes a drum-shaped photoreceptor 1Bk as a first image carrier, a charging unit 2Bk, an exposure unit 3Bk, a developing unit 4Bk, a primary transfer roller 5Bk as a primary transfer unit, and a cleaning unit. 6Bk.

  The four sets of image forming units 10Y, 10M, 10C, and 10Bk include charging means 2Y, 2M, 2C, and 2Bk that rotate around the photosensitive drums 1Y, 1M, 1C, and 1Bk, and image exposure means 3Y, 3M, 3C and 3Bk, rotating developing means 4Y, 4M, 4C, and 4Bk, and cleaning means 5Y, 5M, 5C, and 5Bk for cleaning the photosensitive drums 1Y, 1M, 1C, and 1Bk.

  The image forming units 10Y, 10M, 10C, and 10Bk have the same configuration except that the colors of toner images formed on the photoreceptors 1Y, 1M, 1C, and 1Bk are different, and the image forming unit 10Y is taken as an example in detail. explain.

  The image forming unit 10Y has a charging unit 2Y (hereinafter simply referred to as a charging unit 2Y or a charger 2Y), an exposure unit 3Y, a developing unit 4Y, and a cleaning unit 5Y (around a photosensitive drum 1Y as an image forming body). Hereinafter, the cleaning means 5Y or the cleaning blade 5Y) is simply disposed, and a yellow (Y) toner image is formed on the photosensitive drum 1Y. In the present embodiment, in the image forming unit 10Y, at least the photosensitive drum 1Y, the charging unit 2Y, the developing unit 4Y, and the cleaning unit 5Y are provided so as to be integrated.

  The charging unit 2Y is a unit that applies a uniform potential to the photosensitive drum 1Y. In the present embodiment, a corona discharge type charger 2Y is used for the photosensitive drum 1Y.

  The image exposure means 3Y performs exposure based on the image signal (yellow) on the photosensitive drum 1Y given a uniform potential by the charger 2Y, and forms an electrostatic latent image corresponding to the yellow image. As the exposure means 3Y, a semiconductor laser or light emitting diode having an oscillation wavelength of 350 to 500 nm as used in the description of FIG. 1 can be used as an image exposure light source. Using these image exposure light sources, the exposure dot diameter in the writing direction is narrowed down to 10 to 50 μm, and digital exposure is performed on the organic photoreceptor, so that it is 600 dpi (dpi: the number of dots per 2.54 cm) or more. A high-resolution electrophotographic image of 2500 dpi can be obtained. The surface emitting laser array described above can also be used. Further, an LED composed of light emitting elements arranged in an array in the axial direction of the photosensitive drum 1Y and an imaging element (trade name: Selfoc lens) may be used.

  The image forming apparatus of the present invention is configured by integrally combining the above-described photosensitive member and components such as a developing device and a cleaning device as a process cartridge (image forming unit), and this image forming unit is connected to the apparatus main body. It may be configured to be detachable. In addition, at least one of a charging device, an image exposure device, a developing device, a transfer or separation device, and a cleaning device is integrally supported together with a photosensitive member to form a process cartridge (image forming unit), which is detachable from the apparatus main body. A single image forming unit may be detachable using guide means such as a rail of the apparatus main body.

  The endless belt-like intermediate transfer body unit 7 includes an endless belt-like intermediate transfer body 70 as a second image carrier having a semiconductive endless belt shape that is wound around a plurality of rollers and is rotatably supported.

  Each color image formed by the image forming units 10Y, 10M, 10C, and 10Bk is sequentially transferred onto a rotating endless belt-shaped intermediate transfer body 70 by primary transfer rollers 5Y, 5M, 5C, and 5Bk as primary transfer means. Thus, a synthesized color image is formed. A transfer material P as a transfer material (a support for carrying a fixed final image: for example, plain paper, a transparent sheet, etc.) housed in the paper feed cassette 20 is fed by a paper feed means 21 and a plurality of intermediates. After passing through rollers 22A, 22B, 22C, 22D and registration roller 23, they are conveyed to a secondary transfer roller 5b as a secondary transfer means, and are secondarily transferred onto a transfer material P to transfer a color image all at once. The transfer material P onto which the color image has been transferred is subjected to fixing processing by the fixing unit 24, is sandwiched between paper discharge rollers 25, and is placed on a paper discharge tray 26 outside the apparatus. Here, a transfer support for a toner image formed on a photosensitive member such as an intermediate transfer member or a transfer material is collectively referred to as a transfer medium.

  On the other hand, after the color image is transferred to the transfer material P by the secondary transfer roller 5b as the secondary transfer means, the residual toner is removed by the cleaning means 6b from the endless belt-shaped intermediate transfer body 70 in which the transfer material P is separated by curvature. The

  During the image forming process, the primary transfer roller 5Bk is always in contact with the photoreceptor 1Bk. The other primary transfer rollers 5Y, 5M, and 5C are in contact with the corresponding photoreceptors 1Y, 1M, and 1C, respectively, only during color image formation.

  The secondary transfer roller 5b contacts the endless belt-shaped intermediate transfer body 70 only when the transfer material P passes through the secondary transfer roller 5b.

  Further, the housing 8 can be pulled out from the apparatus main body A through the support rails 82L and 82R.

  The housing 8 includes image forming units 10Y, 10M, 10C, and 10Bk and an endless belt-shaped intermediate transfer body unit 7.

  The image forming units 10Y, 10M, 10C, and 10Bk are arranged in tandem in the vertical direction. An endless belt-shaped intermediate transfer body unit 7 is disposed on the left side of the photoreceptors 1Y, 1M, 1C, and 1Bk in the drawing. The endless belt-shaped intermediate transfer body unit 7 includes an endless belt-shaped intermediate transfer body 70 that can be rotated by winding rollers 71, 72, 73, 74, primary transfer rollers 5Y, 5M, 5C, 5Bk, and cleaning means 6b. Consists of.

  Next, FIG. 3 shows a color image forming apparatus using the organic photoreceptor of the present invention (a copying machine having at least a charging means, an exposure means, a plurality of developing means, a transfer means, a cleaning means, and an intermediate transfer body around the organic photoreceptor. 1 is a cross-sectional view of a configuration of a laser beam printer). The belt-shaped intermediate transfer body 70 uses an elastic body having a medium resistance.

  Reference numeral 1 denotes a rotary drum type photoconductor that is repeatedly used as an image forming body, and is rotationally driven in a counterclockwise direction indicated by an arrow at a predetermined peripheral speed.

  In the rotation process, the photoreceptor 1 is uniformly charged to a predetermined polarity and potential by a charging means (charging process) 2, and then time-series electric digital of image information by an image exposure means (image exposure process) 3 (not shown). An electrostatic latent image corresponding to the yellow (Y) color component image (color information) of the target color image is formed by receiving image exposure by scanning exposure light or the like by a laser beam modulated in accordance with the pixel signal. The

  Then, the electrostatic latent image is developed with yellow toner as the first color by yellow (Y) developing means: developing step (yellow color developing device) 4Y. At this time, the second to fourth developing means (magenta developer, cyan developer, black developer) 4M, 4C, and 4Bk are turned off and do not act on the photosensitive member 1. The first color yellow toner image is not affected by the second to fourth developing units.

  The intermediate transfer member 70 is stretched by rollers 79a, 79b, 79c, 79d, and 79e, and is driven to rotate in the clockwise direction at the same peripheral speed as the photosensitive member 1.

  The yellow toner image of the first color formed and supported on the photosensitive member 1 is applied to the intermediate transfer member 70 from the primary transfer roller 5a in the process of passing through the nip portion between the photosensitive member 1 and the intermediate transfer member 70. The intermediate transfer (primary transfer) is sequentially performed on the outer peripheral surface of the intermediate transfer body 70 by the electric field formed by the primary transfer bias.

  The surface of the photoreceptor 1 after the transfer of the first color yellow toner image corresponding to the intermediate transfer body 70 is cleaned by the cleaning device 6a.

  Similarly, the second color magenta toner image, the third color cyan toner image, and the fourth color black (black) toner image are sequentially superimposed and transferred onto the intermediate transfer body 70 to correspond to the target color image. A superimposed color toner image is formed.

  The secondary transfer roller 5b is supported in parallel with the secondary transfer counter roller 79b so as to be separated from the lower surface portion of the intermediate transfer body 70.

  The primary transfer bias for sequentially superimposing and transferring the first to fourth color toner images from the photosensitive member 1 to the intermediate transfer member 70 has a polarity opposite to that of the toner and is applied from a bias power source. The applied voltage is, for example, in the range of +100 V to +2 kV.

  In the primary transfer process of the first to third color toner images from the photosensitive member 1 to the intermediate transfer member 70, the secondary transfer roller 5b and the intermediate transfer member cleaning means 6b can be separated from the intermediate transfer member 70. .

  When the superimposed color toner image transferred onto the belt-shaped intermediate transfer member 70 is transferred onto the transfer material P, which is the second image carrier, the secondary transfer roller 5b is brought into contact with the belt of the intermediate transfer member 70. At the same time, the transfer material P is fed from the pair of paper registration rollers 23 through the transfer sheet guide to the belt of the intermediate transfer body 70 to the contact nip with the secondary transfer roller 5b at a predetermined timing. A secondary transfer bias is applied to the secondary transfer roller 5b from a bias power source. By this secondary transfer bias, the superimposed color toner image is transferred (secondary transfer) from the intermediate transfer body 70 to the transfer material P which is the second image carrier. The transfer material P that has received the transfer of the toner image is introduced into the fixing means 24 and heated and fixed.

  The image forming apparatus of the present invention is generally applicable to electrophotographic apparatuses such as electrophotographic copying machines, laser printers, LED printers, and liquid crystal shutter printers, and further displays, recordings, light printing, plate making and facsimiles using electrophotographic technology. The present invention can be widely applied to such devices.

EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated in detail, the aspect of this invention is not limited to this. In the following text, “part” means “part by mass”.
Example 1
Production of Photoreceptor 1 Photoreceptor 1 was produced as follows.

The surface of the cylindrical aluminum support was cut to prepare a conductive support having a ten-point surface roughness Rz = 0.7 (μm).
<Intermediate layer>
The following intermediate layer dispersion is diluted twice with the same mixed solvent, and is allowed to stand overnight and then filtered (filter; rigesh mesh filter made by Nippon Pole Co., Ltd., nominal filtration accuracy: 5 microns, pressure: 50 kPa). Produced.

(Preparation of intermediate layer dispersion)
Binder resin: (Exemplary polyamide N-1) 1 part (1.00 volume part)
N-type semiconductive particles: rutile titanium oxide A1 (primary particle size 35 nm; copolymer of methylhydrogensiloxane and dimethylsiloxane (molar ratio 1: 1), in an amount of 5% by mass of the total mass of titanium oxide. Surface treatment) 3.5 parts (1.0 part by volume)
Ethanol / n-propyl alcohol / THF (= 45/20/30 mass ratio) 10 parts The above components were mixed and dispersed in a batch system for 10 hours using a sand mill disperser to prepare an intermediate layer dispersion. .

  The intermediate layer coating solution was applied on the conductive support by a dip coating method and dried at 120 ° C. for 30 minutes to form an intermediate layer having a dry film thickness of 1.0 μm.

<Charge generation layer: CGL>
Charge generation substance (CGM): Sublimation purified pigment (CGM-1) obtained in Synthesis Example 1 7 parts Binder resin; Polyvinyl butyral resin “ESREC BL-X” (manufactured by Sekisui Chemical Co., Ltd.) 1 part 2-butanone / cyclohexanone = 4/1 250 parts The above composition was mixed and dispersed using a sand mill apparatus filled with glass beads to prepare a charge generation layer coating solution. This coating solution was applied by a dip coating method to form a charge generation layer having a dry film thickness of 0.5 μm on the intermediate layer.

<Charge transport layer (CTL)>
Charge transport material (CTM): Exemplified compound CTM-1 225 parts Polycarbonate (Z300: manufactured by Mitsubishi Gas Chemical Co., Inc.) 300 parts Antioxidant (AO-1 below) 6 parts THF / toluene mixed solution (volume ratio 3/1 mixed) 2000 parts Silicon oil (KF-54: manufactured by Shin-Etsu Chemical Co., Ltd.) 1 part was mixed and dissolved to prepare a charge transport layer coating solution. This coating solution was applied onto the charge generation layer by a dip coating method and dried at 110 ° C. for 70 minutes to form a charge transport layer 1 having a dry film thickness of 20.0 μm.

Production of Photoreceptor 2 Photoreceptor 2 was produced in the same manner as in production of Photoreceptor 1 except that CGM-1 as the charge generation material was changed to the sublimation purified pigment (CGM-2) obtained in Synthesis Example 2. .

Production of Photoreceptor 3 Photoreceptor 3 was produced in the same manner as in production of Photoreceptor 1 except that CGM-1 as the charge generation material was changed to the sublimation purification pigment (CGM-3) obtained in Synthesis Example 3. .

Production of Photoreceptor 4 In production of Photoreceptor 2, polyvinyl butyral resin “ESREC BL-X” (manufactured by Sekisui Chemical Co., Ltd.), which is a binder resin for the charge generation layer, is replaced with polyvinyl butyral resin “ESREC BX-1” (manufactured by Sekisui Chemical Co., Ltd.). A photoconductor 4 was produced in the same manner except that it was changed to.

Production of Photoreceptor 5 In the production of Photoreceptor 2, the charge generating layer binder resin was changed in the same manner except that the amount of polyvinyl butyral resin “S-LEC BL-X” (manufactured by Sekisui Chemical Co., Ltd.) was changed from 1 part to 2 parts. A photoreceptor 5 was prepared.

Production of Photoreceptor 6 Photoreceptor 6 was produced in the same manner as in production of Photoreceptor 2, except that the CTM of the charge transport layer was changed from CTM-1 to CTM-6.

Production of Photoreceptor 7 Photoreceptor 7 was produced in the same manner as in production of Photoreceptor 2 except that the CTM of the charge transport layer was changed from CTM-1 below to CTM-10 below.

Photoconductor 8 (Comparative example; no binder)
Photoreceptor 8 was produced in the same manner as in the production of photoconductor 2 except that the binder resin in the charge generation layer was removed.

Photoreceptor 9 (Comparative Example: Change of dispersion solvent)
Photoconductor 9 was prepared in the same manner as in the preparation of photoconductor 2, except that the dispersion solvent of the charge generation layer was changed from 2-butanone / cyclohexanone = 4/1 to 1,2-dichloroethane.

Photoconductor 10 (comparative example; one-step sublimation purification)
Photoreceptor 10 was produced in the same manner except that CGM-1 as the charge generation material was changed to the one-step sublimation purified pigment (CGM-4) obtained in Synthesis Example 4 below.

Synthesis example 4 (comparative example; one-step sublimation)
The crude pigment product obtained in Synthesis Example 2 (5.0 g) was placed in a graphite crucible placed in a vacuum vapor deposition apparatus, and heated to 480 ° C. under a reduced pressure of about 133.3 Pa to 13.3 Pa. It condensed on the board | substrate arrange | positioned 15 cm above the evaporation source, and obtained 3.5 g of sublimates (CGM-4).

Photoreceptor 11 (Comparative example: Re-purification after sublimation purification)
Photoreceptor 11 was produced in the same manner except that CGM-1 as the charge generation material was changed to the sublimation purified atomized pigment (CGM-5) obtained in Synthesis Example 5 below.

Synthesis example 5
1 part of the sublimation purified pigment obtained in Synthesis Example 2 was dissolved in 30 parts of chlorosulfuric acid and poured into 500 g of ice. After filtration, it was washed with water and dried until the washing solution became neutral to obtain a purified atomized pigment (CGM-5).

Photoreceptor 12 (Comparative Example; Evaporation)
In the production of the photoconductor 1, the sublimation purification pigment obtained in Synthesis Example 2 was used as the charge generation layer in a molybdenum boat, and the vacuum generation film was formed under a reduced pressure of about 13.3 Pa to 1.3 Pa. Thus, a photoreceptor 12 was produced.

Preparation of Samples for Measuring Spectral Absorption Spectra of Charge Generation Layer (CGL-1 to CGL-12) The charge generation layers of the photoconductor 1 to photoconductor 12 are coated on a transparent polyester film with the same film thickness as the photoconductor. Samples for spectral absorption spectrum measurement; CGL-1 to CGL-12 (CGL corresponding to the photoreceptors 1 to 12 respectively) were prepared by vapor deposition.

<< Evaluation 1 >>
Spectral absorption spectra of the charge generation layers (CGL-1 to CGL-12) were measured by the method described above, and whether or not there was an absorption peak in each region of 400 to 440 nm (Abs1) and 530 to 600 nm (Abs2), and Table 1 shows the magnitude of the absorption peak at 400 to 440 nm and the absorption peak at 530 to 600 nm. Representative examples of these absorption spectra are shown in FIGS.

  In Table 1, ○ has an absorption peak between 400 to 440 nm (Abs1) and 530 to 600 nm (Abs2), and × represents an absorption peak between 400 to 440 nm (Abs1) and 530 to 600 nm (Abs2). Indicates that it does not exist.

<< Evaluation 2 >>
The photoreceptor prepared above was evaluated as follows using an electrostatic copying paper test apparatus (manufactured by Kawaguchi Electric Co., Ltd .: EPA-8100).

(sensitivity)
Charge the surface potential of the photoconductor with a corona charger so as to be −700 V, then expose with 400 nm monochromatic light separated by a monochromator, measure the amount of light necessary for the surface potential to decay to −350 V, Sensitivity (E1 / 2) was determined.

  Similarly, the sensitivity in 450 nm and 500 nm monochromatic light was measured.

(Repeat characteristics)
Next, the initial dark portion potential (Vd) and the initial bright portion potential (Vl) are set to around −700 V and −200 V, respectively, and charging and exposure are repeated 3000 times using a monochromatic light of 450 nm, and the fluctuation amount of Vd and Vl ( ΔVd, ΔVl) were measured.

  The results are shown in Table 1.

  In the following table, a minus sign represents a decrease in potential, and a plus sign represents an increase in potential.

(Image evaluation)
Using Konica Minolta's digital multifunction machine bizhub 920 remodeling machine (using a 405 nm semiconductor laser as the image exposure light source, exposing at 1200 dpi with a beam diameter of 30 μm and modifying the process speed to 400 mm / sec), the copying The photoreceptors 1 to 12 were mounted on the machine and evaluated. Evaluation items and evaluation criteria are shown below.

Evaluation of 1-dot line A 1-dot line and a solid black image were produced on a white A4 paper, and evaluated according to the following criteria.

◎: 1 dot line is reproduced continuously, solid image density is 1.2 or higher (good)
○: 1 dot line is reproduced continuously, but solid image density is less than 1.2 to 1
. 0 or more (no problem in practical use)
×: Even if one dot line is cut and reproduced, or one dot line is continuously reproduced, the solid black image density is less than 1.0 (problem in practical use)
Evaluation of 2-dot line A 2-dot white line was produced in a solid black image and evaluated according to the following criteria.

A: The white line of 2 dot lines is reproduced continuously, and the image density of solid black is 1.2 or more (good)
○: The white line of 2 dot lines is reproduced continuously, but the solid image density is less than 1.2 to 1.0 or more (no problem in practical use)
X: Even if the white line of 2 dot lines is cut and reproduced, or the white line of 2 dot lines is reproduced continuously, the solid image density is less than 1.0 (there is a problem in practical use)
The above-mentioned solid image density is measured using RD-918 manufactured by Macbeth. The relative reflection density was measured with the paper reflection density set to “0”. The results are shown in Table 1.

  As apparent from Tables 1 and 2, the charge generation layer contains a binder resin and a charge generation material of the compound represented by the general formula (1), and the spectrum of the charge generation layer is 400 to 440 nm. The organic photoconductors 1 to 7 have an absorption peak in each region of 530 to 600 nm, and the absorption peak intensity between 400 to 440 nm is higher than the absorption peak intensity between 530 to 600 nm. It has excellent sensitivity characteristics and repeatability for 400 to 500 nm irradiation light such as laser light, and the reproducibility of 1 dot line and 2 dot line in image evaluation using 405 nm short wavelength laser light. Are better.

  On the other hand, in the photoreceptor 8 that does not use the binder resin in the charge generation layer, the dispersibility of the pigment is deteriorated, and the sensitivity characteristics, the repeated potential characteristics, and the reproducibility of the 1-dot line and 2-dot line are also deteriorated.

  Further, in the photoconductor 9 using 1,2-dichloroethane as the dispersion solvent of the charge generation layer, the magnitude relation of the peak intensity is reversed, and the sensitivity characteristic and the reproducibility of one dot line are lowered.

  In addition, the sublimation purification of the charge generation substance and the one-step sublimation purification photoreceptor 10 also reverse the magnitude relationship between the peak intensities, deteriorate the sensitivity characteristics and the repetition characteristics, and reduce the reproducibility of one dot line.

  In addition, it is considered that the photoconductor 11 purified by sublimation purification of the charge generation material and further subjected to chemical treatment seems to have greatly changed the crystal structure of the pigment. The reproducibility of the 1-dot line and 2-dot line also deteriorates.

  Further, in the photoconductor 12 in which the charge generation layer is formed by vapor deposition, no absorption peak appears in each of the spectral spectra of 400 to 440 nm and 530 to 600 nm. The dot line reproducibility is also degraded.

Evaluation 3
The image evaluation conditions in the evaluation 2 are the same as those in the evaluation 2 except that the beam diameter in the image evaluation conditions is changed from 30 μm to 18 μm, 1200 dpi is changed to 1800 dpi, and the photoconductors 1, 2 and 3 are used. Went.

  As a result of the evaluation, all the images obtained from the photoconductors 1, 2 and 3 had good reproducibility of the 1-dot line and 2-dot line.

Evaluation 4
Full-color digital multifunction machine bizhub C550 remodeling machine having a commercially available intermediate transfer body having the structure shown in FIG. 2 for the above photoconductors 1, 2, and 3 (remodeling machine manufactured by Konica Minolta Business Technologies, Inc., image of exposure means) A 405 nm semiconductor laser was used as the exposure light source, 1200 dpi exposure was performed with a beam diameter of 30 μm, and the process speed was modified to 220 mm / sec), and color images were evaluated.

  The evaluation was the same as the image evaluation in the evaluation 2, and the 1 dot line evaluation and the 2 dot line evaluation were performed. However, all the color images obtained from the photoconductors 1, 2 and 3 were 1 dot line. In addition, it was possible to obtain a color image with good reproducibility of the two-dot lines and good color reproducibility.

Evaluation 5
A full-color digital multifunction machine bizhub C550 remodeling machine having a commercially available intermediate transfer body having the structure shown in FIG. 2 for the above photoconductors 1, 2, and 3 (remodeling machine manufactured by Konica Minolta Business Technologies Co., Ltd., exposure means) A surface-emitting laser array was used, and each laser beam diameter was 30 μm, 1200 dpi exposure was performed, and the process speed was modified to 220 mm / sec))), and color images were evaluated.

Surface emitting laser array A surface emitting laser array as illustrated in FIG. 4 was used. The surface emitting laser array has an oscillation wavelength of 405 nm and is arranged so that the light emitting points do not overlap in the vertical (sub-scanning direction) and the horizontal (main scanning direction).

  A surface emitting laser array having 36 light emitting points of 6 × 6 matrix in each of vertical and horizontal directions was used. In actual use, it depends on the control condition of the computer [2 to the nth power (25 in this case)]. Therefore, 32 are used instead of 36.

  The evaluation was the same as the image evaluation in the evaluation 2, and the 1 dot line evaluation and the 2 dot line evaluation were performed. However, all the color images obtained from the photoconductors 1, 2 and 3 were 1 dot line. In addition, it was possible to obtain a color image with good reproducibility of the two-dot lines and good color reproducibility.

1 is a schematic view in which functions of an image forming apparatus of the present invention are incorporated. 1 is a cross-sectional configuration diagram of a color image forming apparatus showing an embodiment of the present invention. 1 is a cross-sectional view of a color image forming apparatus using an organic photoreceptor of the present invention. It is a schematic diagram of a surface emitting laser array. 2 is a diagram of a spectral absorption spectrum of a charge generation layer of the photoreceptor 1. FIG. 3 is a diagram of a spectral absorption spectrum of a charge generation layer of the photoreceptor 2. FIG. 3 is a diagram of a spectral absorption spectrum of a charge generation layer of the photoreceptor 3. FIG. FIG. 4 is a spectral absorption spectrum of the charge generation layer of the photoreceptor 9. 3 is a diagram of a spectral absorption spectrum of a charge generation layer of the photoreceptor 11. FIG. 3 is a diagram of a spectral absorption spectrum of a charge generation layer of the photoreceptor 12. FIG.

Explanation of symbols

10Y, 10M, 10C, 10Bk Image forming unit 1Y, 1M, 1C, 1Bk Photoconductor 2Y, 2M, 2C, 2Bk Charging unit 3Y, 3M, 3C, 3Bk Exposure unit 4Y, 4M, 4C, 4Bk Developing unit L Light emitting point

Claims (6)

In an organic photoreceptor having a charge generation layer and a charge transport layer on a conductive support, the charge generation layer contains a binder resin and a compound represented by the following general formula (1), and the spectrum of the charge generation layer: There has an absorption peak in each region of 400~440nm and 530～600Nm, the absorption peak intensity between the 400~440nm is rather high than the absorption peak intensity between 530～600Nm, and the following general formula (1) An organic photoreceptor, wherein the compound is a mixture of two or more compounds having different n .
(In general formula (1), n is an integer of 1 to 6) The organophotoreceptor according to claim 1, wherein the charge transport layer contains a compound represented by the following general formula (2) .

(In the general formula (2), R ₁ and R ₂ each independently represent an alkyl group or an aryl group, R ₁ and R ₂ are together, may form a ring structure .R ₃ and R ₄ are each independently a hydrogen atom, an alkyl group or an aryl group, or different from each .Ar ₁ to Ar ₄ are the same Ar ₁ to Ar ₄ is representing each substituted or unsubstituted aryl group Ar ₁ and Ar ₂ , Ar ₃ and Ar ₄ may be bonded to form a ring structure, and m and n represent an integer of 1 to 4.) The organic photoconductor according to claim 1, a charging unit for charging the organic photoconductor, an exposure unit for exposing the organic photoconductor charged by the charging unit to form an electrostatic latent image, and A developing unit configured to develop the electrostatic latent image with toner to form a toner image; and a transfer unit configured to transfer the toner image from the organic photoreceptor to a transfer medium. An image forming apparatus having an exposure diameter of 10 to 50 μm . The organic photoconductor according to claim 1, a charging unit for charging the organic photoconductor, an exposure unit for exposing the organic photoconductor charged by the charging unit to form an electrostatic latent image, and A developing unit that develops the electrostatic latent image with toner to form a toner image; and a transfer unit that transfers the toner image from the organic photoreceptor to a transfer medium. The exposure unit has a wavelength of 350 to 500 nm. An image forming apparatus comprising monochromatic light of an area as an exposure light source . The organic photoconductor according to claim 1, a charging unit for charging the organic photoconductor, an exposure unit for exposing the organic photoconductor charged by the charging unit to form an electrostatic latent image, and a developing unit for forming a toner image an electrostatic latent image is developed with toner, the toner image and a transfer means for transferring to a transfer medium from the organic photoreceptor, wherein the exposure means is vertically and horizontally three or more A multi-beam method comprising a surface emitting laser array having a laser beam emission point in the range of 350 to 500 nm as an exposure light source, and scanning the laser beam emission point on the organic photoreceptor to form the electrostatic latent image an image forming apparatus characterized in that. The image forming apparatus according to claim 3, wherein a writing density is 1200 dpi or more .