EP0709747A2 - Elektrofotografisches Verfahren, welches fotoempfindliches Material verwendet - Google Patents

Elektrofotografisches Verfahren, welches fotoempfindliches Material verwendet Download PDF

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Publication number
EP0709747A2
EP0709747A2 EP95307715A EP95307715A EP0709747A2 EP 0709747 A2 EP0709747 A2 EP 0709747A2 EP 95307715 A EP95307715 A EP 95307715A EP 95307715 A EP95307715 A EP 95307715A EP 0709747 A2 EP0709747 A2 EP 0709747A2
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Prior art keywords
photosensitive material
light
exposure
amount
potential
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Granted
Application number
EP95307715A
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English (en)
French (fr)
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EP0709747B1 (de
EP0709747A3 (de
Inventor
Mitsuji C/O Mita Industrial Co. Ltd. Tsujita
Nariaki C/O Mita Industrial Co. Ltd. Tanaka
Takashi C/O Mita Industrial Co. Ltd. Terada
Takuji C/O Mita Industrial Co. Ltd. Terada
Ichiro C/O Mita Industrial Co. Ltd. Yamazato
Eiichi C/O Mita Industrial Co. Ltd. Miyamoto
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Kyocera Document Solutions Inc
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Mita Industrial Co Ltd
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Publication of EP0709747A3 publication Critical patent/EP0709747A3/de
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Publication of EP0709747B1 publication Critical patent/EP0709747B1/de
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    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G13/00—Electrographic processes using a charge pattern
    • G03G13/22—Processes involving a combination of more than one step according to groups G03G13/02 - G03G13/20
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—Charge-receiving layers
    • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G15/00—Apparatus for electrographic processes using a charge pattern
    • G03G15/06—Apparatus for electrographic processes using a charge pattern for developing
    • G03G15/065—Arrangements for controlling the potential of the developing electrode

Definitions

  • the present invention relates to an electrophotographic method by using a photosensitive material and, particularly, an organic photosensitive material and utilizing high-sensitivity characteristics with a small amount of exposure to light. More specifically, the invention relates to an electrophotographic method by which a photosensitive material and, particularly, a photosensitive material in which the loss of electric charge becomes mild at around a half amount of exposure to light is adapted to a high-speed electrophotographic system without generating fogging.
  • a photosensitive material for electrophotography is electrically charged, exposed to image-bearing light to form electrostatic latent image, which is then developed with toner in a state where a developing bias voltage is applied thereto, and the toner image that is formed is transferred to a transfer paper followed by fixing to form an image.
  • organic photosensitive materials include a laminated photosensitive material of the function-separated type in which a charge-generating agent (CGM) and a charge-transporting agent (CTM) are laminated as separate layers, and a single-layer photosensitive material in which CGM and CTM are provided as a single dispersion layer.
  • CGM charge-generating agent
  • CTM charge-transporting agent
  • the single-layer photosensitive material has a charge-generating agent that is dispersed in a resin medium in which a charge-transporting agent is dissolved.
  • the layer of charge-generating agent has the charge-generating agent dispersed in the resin medium.
  • Fig. 1 which illustrates a relationship between the surface potential and the time
  • the potential in a dark portion (D) is attenuated only slightly in response to dark attenuation whereas the potential in a bright portion (L) is quickly attenuated in response to light attenuation, whereby a potential contrast adapted to developing is formed.
  • the sensitivity of the photosensitive material corresponds to the rate of light attenuation and is, generally, evaluated in terms of the amount of exposure to light needed for halving the potential relative to the initial potential of before being exposed to light, i.e., evaluated in terms of a half amount of exposure to light (lux x sec).
  • the electric charge quickly attenuates up to nearly the half amount of exposure to light. As the amount of exposure exceeds the half amount of exposure to light, however, the electric charge attenuates mildly.
  • the amount of exposure to light must be set to a considerably large value compared with the half amount of exposure to light.
  • a source of light having a large output is necessary and a large cooling fan is needed to remove the heat generated by the source of light, resulting in an increase in the cost of the apparatus and the cost of electric power.
  • exposing an organic photosensitive material to a large quantity of light causes the photosensitive material to be deteriorated.
  • an extended period of time is required for the step of exposure to light imposing limitation on the speed of copying and on the printing speed in the facsimile or laser printer.
  • the object of the present invention is to provide an electrophotographic metnod which is capable of forming vivid image without fogging and, particularly, capable of forming image with a small amount of exposure to light by utilizing high-sensitivity characteristics of a photosensitive material in the zone of a small amount of exposure to light.
  • Another object of the present invention is to provide an electrophotographic method of a type which is realized using a cheaply constructed device and consumes small amounts of resources and small amounts of energy by using an organic photosensitive material.
  • an electrophotographic method comprising electrically charging a photosensitive material, exposing the photosensitive material to image-bearing light to form electrostatic latent image, and developing the electrostatic latent image in a state where a developing bias voltage is applied, wherein said developing bias voltage is set to a potential which has a polarity same as the polarity of the electric charge in the photosensitive material, and is higher than a potential (hereinafter often called as point-of-intersection voltage (E H )) that corresponds to a point where a curve approximating the zone of a large amount of exposure to light and a curve approximating the zone of a small amount of exposure to light in a light attenuation characteristics curve intersect each other.
  • E H point-of-intersection voltage
  • the present invention can be advantageously adapted to a photosensitive material in which the loss of electric charge becomes mild at around a half amount of exposure to light and, particularly, to an organic photosensitive material of the type in which a charge-generating agent is dispersed and, preferably, to a single-dispersion-layer photosensitive material in which a charge-generatin g substance is dispersed in a resin medium that includes a charge-transporting substance and, most desirably, to a single-dispersion-layer photosensitive material of the positively charged type.
  • a curve ⁇ represents characteristics of a single-layer organic photosensitive material
  • a curve ⁇ represents characteristics of a laminated-layer organic photosensitive material
  • a curve ⁇ represents characteristics of an amorphous silicon photosensitive material
  • the developing bias potential (EB) is set to be higher than a potential that corresponds to a point of intersection H where a line F approximating the zone of a large amount of exposure to light of a light attenuation characteristics curve ⁇ ( ⁇ or ⁇ ) of a photosensitive material intersects a line G approximating the zone of a small amount of exposure to light in Fig. 3 where the light attenuation characteristics curve of Fig. 2 are plotted on a logarithmic scale (though the point of intersection H is shown concerning the curve ⁇ only to simplify the drawing, it should be noted that the same also holds true even for other curves).
  • the line F approximating the zone of a large amount of exposure to light represents high sensitivity characteristics in the zone of a small amount of exposure to light of the photosensitive material and the line G approximating the zone of a small amount of exposure to light represents low sensitivity characteristics in the zone of a large amount of exposure to light of the photosensitive material.
  • the developing bias potential (EB) is set to be higher than a potential that corresponds to the point of intersection H of these two lines in order to effectively utilize high sensitivity characteristics in the zone of a small amount of exposure to light thereby to form an electrostatic latent image of a high contrast with a small amount of exposure to light or within a short exposure time.
  • the light attenuation in the photosensitive material varies as an exponential function and can be approximated by the above-mentioned formula (1) which is the sum of two exponential functions. That is, the absolute value (volts) of potential on the surface of the photosensitive material with the amount I of exposure to light (lux ⁇ sec) is measured relative to the absolute value Vo (volts) of the initial potential on the surface of the photosensitive material, and the measured values are substituted for the formula (1) to find values of coefficients A, B, C and D.
  • a and C are such that their sum is 1.
  • Light attenuation characteristics (light sensitivity characteristics) of potential of the photosensitive material can be represented by values of four coefficients A, B, C and D. It can be said that the photosensitive material having a large coefficient A is highly sensitive and that the photosensitive material having a large coefficient C loses the electric charge at a small rate when it is exposed to large amounts of light.
  • the coefficients A and C are numbers of from 0.7 to 1 and from 0 to 0.3, respectively, under the condition that their sum is 1, that the coefficient B is from 0.1 to 1.5 lux ⁇ sec-1 and that the coefficient D is from 0.01 to 0.2 lux ⁇ sec ⁇ 1.
  • a and C affect seriously.
  • the coefficient A has a value of from 0.75 to 0.85 and in a laminated-layer organic photosensitive material, the coefficient A has a value of from 0.9 to 0.80.
  • the coefficient A has a value of from 0.95 to 0.85.
  • the present invention can be applied particularly advantageously to a photosensitive material which loses the electric charge mildly at around a half amount of exposure to light, i.e., to an organic photosensitive material in which the charge-generating agent is dispersed and, particularly, to a single-dispersion-layer photosensitive material in which the charge-generating substance is dispersed in a resin medium which include a charge-transporting substance and, most desirably, to a single-dispersion-layer photosensitive material of the positively charged type.
  • the suitable developing bias potential (EB) can be found by a graphic solution from a light attenuation characteristics curve of the photosensitive material shown in Fig. 2 or can be found from a point of intersection H of a line F approximating the zone of a large amount of exposure to light and a line G approximating the zone of a small amount of exposure to light based upon the plotting of logarithmic values of the surface potential and the amount of exposure to light shown in Fig. 3.
  • the method of Fig. 3 makes it possible to find the suitable developing bias potential (EB) more correctly.
  • the developing bias potential (EB) is given by the above-mentioned formula (2), wherein K gives a gradient of the line F approximating the zone of a small amount of exposure to light and P gives a gradient of the line G approximating the zone of a large amount of exposure to light.
  • a surface potential of 0.9 VoA On the side of the zone of a small amount of exposure to light, there are employed a surface potential of 0.9 VoA, the amount of exposure to light corresponding thereto, a surface potential of 0.7 VoA and the amount of exposure to light corresponding thereto. This is because they give a good curve F approximating the zone of a small amount of exposure to light.
  • a surface potential of 0.9 VoC On the side of the zone of a large amount of exposure to light, similarly, there are employed a surface potential of 0.9 VoC, the amount of exposure to light corresponding thereto, a surface potential of 0.8 VoC and the amount of exposure to light corresponding thereto. This is because they give a good curve G approximating the zone of a large amount of exposure to light.
  • m is a number which is not smaller than 1.5 and, preferably, which lies over a range of from 1.5 to 4.0.
  • m is smaller than the above range, the fogging density increases, which is not desirable as demonstrated in Example appearing later.
  • m is too great, on the other hand, there result carrier trail and drop in the image density, which are not desirable, either.
  • the amount of exposure to light in a bright portion is so set that the residual potential (ER) at the bright portion is lower than the bias potential (EB).
  • setting the developing bias potential (EB) to a large value means that the residual potential (ER) at the bright portion can be set to a large value during the exposure to light which, then, means that the amount of exposure to light or the exposure time can be decreased.
  • the present invention requires a source of light of a small output and a cooling fan of a small size for removing the heat from the source of light, making it possible to decrease the cost of the apparatus and the power cost. Moreover, since the organic photosensitive material needs be irradiated with a small amount of light, the photosensitive material is less deteriorated with light, which is an advantage. When a customary source of light is used, furthermore, the step of exposure to light is accomplished within short periods of time, making it possible to greatly increase the copying speed, printing speed of a facsimile and printing speed of a laser printer.
  • the amount of exposure to light at the bright portion is so determined that the residual potential (ER) at the bright portion satisfies the above-mentioned formula (7) though it may vary depending upon a light attenuation characteristics curve of potential of the photosensitive material, applied bias potential, and developing sensitivity characteristics of the photosensitive material and the developing agent.
  • ED0 a potential at which the fogging density becomes substantially zero
  • n when n is smaller than 0.4, fogging in the white portion increases, which is not desirable.
  • n is greater than 2.5, on the other hand, no particularly distinguished merit is obtained in regard to preventing fogging but resulting in an increase in the amount of exposure to light, which is not desirable, either.
  • a photosensitive layer and, particularly, an organic photosensitive layer 2 is provided on the surface of a metal drum 1 that is rotated.
  • a corona charger 3 for main charging, a lamp 4, a mechanism for exposure to image-bearing light comprising a document-support transparent plate 5 and an optical system 6, a developing mechanism 8 having a developing agent 7, a corona charger 9 for transferring the toner, a corona charger 10 for separating the paper, a lamp 11 for removing electric charge, and a cleaning mechanism 12 in the order mentioned.
  • the photosensitive layer 2 is electrically charged by the corona charger 3 to a predetermined polarity.
  • the document 13 to be copied is illuminated with the lamp 4, so that the photosensitive layer 2 is exposed to light image of the document via the optical system 6 thereby to form an electrostatic latent image corresponding to the document image.
  • the electrostatic latent image is visualized through the developing mechanism 8 to form a toner image.
  • a transfer paper 14 is so fed as to come into contact with the surface of the drum at a position of the charger 9 for transferring the toner, and the back surface of the transfer paper 14 is subjected to the corona charging of a polarity same as that of the electrostatic image to transfer the toner image onto the transfer paper 14.
  • the transfer paper 14 onto which the toner image is transferred is electrostatically peeled off the drum as the electric charge is removed by the corona charger 10 for separation and is sent to a processing zone such as fixing zone (not shown). Residual charge is removed from the photosensitive layer 2 after the toner has been transferred as it is exposed over its whole surface to the light from the lamp 11 for removing electric charge and, then, the residual toner is removed by the cleaning mechanism 12.
  • the developing device 8 which is shown on an enlarged scale in Fig. 6 includes a toner feed hopper 21, a toner feed roller 22, a developing agent stirrer roller 23, and a cylindrical developing agent conveyer sleeve 25 containing a magnet 24 in which N-pole and S-pole are alternatingly arranged. On the side of feeding the developing agent, there is provided a blade 26 for trimming the ear of the magnetic brush on the sleeve to a predetermined length.
  • At least either the magnet 24 or the sleeve 25 is allowed to rotate, and the direction of conveying the magnetic brush may be either the same as or opposite to the drum 1 at a position where it is in contact therewith.
  • the sleeve 25 is made of a nonmagnetic electrically conducting material such as aluminum, and a bias power source 27 is connected to the sleeve 25 so that a predetermined developing bias potential is applied to the developing sleeve 25, the developing bias potential having a polarity same as the polarity of the electric charge on the surface of the photosensitive material.
  • the exposure to image-bearing light is effected by a mechanism for exposure to image-bearing light constituted by the lamp 4, document-support transparent plate 5 and optical system 6.
  • the exposure to image-bearing light can also be effected using an exposure device based upon a widely known laser beam or an array of light-emitting diodes (LEDs).
  • developing is effected by setting the developing bias potential (EB) applied across the sleeve 25 and the photosensitive drum 1 to be greater than a potential that corresponds to a point of intersection H (Fig. 3) of a line approximating the zone of a large amount of exposure to light in the light attenuation characteristics curve of the photosensitive layer 2 and the line approximating the zone of a small amount of exposure to light.
  • the bias voltage (EB) is desirably such that the value m in the above-mentioned formula (2) is not smaller than 1.0 and, particularly, lies over a range of from 1.0 to 2.0.
  • the amount of exposure to light at the bright portion is so set that the residual potential (ER) at the bright portion becomes smaller than the bias potential (EB) and, more preferably, that the value n in the formula (7) is from 0.4 to 2.5 and, particularly, from 0.5 to 2.0.
  • the photosensitive material used in the present invention may be either an organic photosensitive material or an inorganic photosensitive material provided it satisfies the above-mentioned formula (1).
  • an organic photosensitive material and, particularly, by an organic photosensitive material in which a charge-generating agent is dispersed in a resin medium and, particularly, distinguished effects are exhibited by a single-dispersion-layer photosensitive material which contains a charge-transporting agent and, particularly, a positive hole-transporting agent and a charge-generating agent in a resin medium.
  • the photosensitive material of the present invention is allowable to use as a matter of course, as well as to use a laminated-layer photosensitive material of a charge-transporting layer containing a charge-transporting agent and a charge-generating layer containing a charge-generating agent.
  • the charge-generating layer (CGL) and the charge-transporting layer (CTL) may be laminated in this order or in an opposite order.
  • Examples of the charge-generating agent include selenium, selenium-tellurium, amorphous silicon, pyrylium salt, azo pigment, dis-azo pigment, tris-azo pigment, anthanthrone pigment, phthalocyanine pigment, indigo pigment, threne pigment, toluidine pigment, pyrazoline pigment, pyranthrone pigment, perylene pigment and quinacridone pigment, which may be used in a single kind or in a mixture of two or more kinds to exhibit an absorption wavelength over a desired region.
  • phthalocyanine pigment perylene pigment and dis-azo pigment are preferred.
  • resins can be used as resin media for dispersing the charge-generating agent.
  • examples include olefin polymers such as styrene polymer, acrylic polymer, styrene-acrylic polymer, ethylene-vinyl acetate copolymer, polypropylene, ionomer, etc. and polyvinyl chloride, vinyl chloride-vinyl acetate copolymer, polyester, alkyd resin, polyamide, polyurethane, epoxy resin, polycarbonate, polyarylate, polysulfone, dialylphthalate resin, silicone resin, ketone resin, polyvinyl butyral resin, polyether resin and phenolic resin, and photocurable resins such as epoxyacrylate.
  • olefin polymers such as styrene polymer, acrylic polymer, styrene-acrylic polymer, ethylene-vinyl acetate copolymer, polypropylene, ionomer, etc.
  • polyvinyl chloride
  • binder resins may be used in a single kind or in a mixture of two or more kinds.
  • Preferred resins are styrene polymer, acrylic polymer, styrene-acrylic polymer, polyester, alkyd resin, polycarbonate, polyarylate, etc.
  • a particularly preferred resin is a polycarbonate derived from a phosgene and bisphenols represented by the following general formula (8),
  • the charge transporting agent (CTM) may have electron-transporting property or positive hole-transporting property. Or, they may be used in combination. Suitable examples include electron attractive substances such as paradiphenoquinone derivatives, benzoquinone derivatives, naphthoquinone derivatives, tetracyanoethylene, tetracyanoquinodimethane, chloroanil, bromoanil, 2,4,7-trinitro-9-fluorenone, 2,4,5,7-tetranitro-9-fluorenone, 2,4,7-trinitro-9-dicyanomethylene fluorenone, 2,4,5,7-tetranitroxanthone, and 2,4,8-trinitrothioxanthone, as well as high molecules derived from those electron attractive substances.
  • electron attractive substances such as paradiphenoquinone derivatives, benzoquinone derivatives, naphthoquinone derivatives, tetracyanoethylene, tetracyanoquinodimethane, chloroanil, bromoanil
  • paradiphenoquinone derivatives and, particularly, asymmetrical paradiphenoquinone derivatives are excellent in solubility and in electron-transporting property.
  • substituents R5, R6, R7 and R8 exist in asymmetrical forms.
  • suitable examples include 3,5-dimethyl-3',5'-di-t-butyldiphenoquinone, 3,5-dimethoxy-3',5'-di-t-butyldiphenoquinone, 3,3'-dimethyl-5,5'-di-t-butyldiphenoquinone, 3,5'-dimethyl-3',5-di-t-butyldiphenoquinone, 3,5,3',5'-tetramethyldiphenoquinone, 2,6,2',6'-tetra-t-butyldiphenoquinone, 3,5,3',5'-tetraphenyldiphenoquinone, 3,5,3',5'-tetracyclohexyldiphenoquinone and the like.
  • These diphenoquinone derivatives have low molecular symmetry, exhibit small mutual action among the molecules and are excellent in solubility.
  • the positive hole-transporting substances the following substances have been known. Among them, those compounds having excellent solubility and positive hole-transporting property are used:
  • the benzidine transporting agents and, particularly, the transporting agents represented by the general formula (10),
  • the charge-generating agent (CGM) is contained in the photosensitive layer in an amount of from 1 to 7% by weight and, particularly, from 2 to 5% by weight per the solid component and the charge-transporting agent (CTM) is contained in the photosensitive layer in an amount of from 20 to 70% by weight and, particularly, from 25 to 60% by weight per the solid component.
  • ET electron-transporting agent
  • HT positive hole-transporting agent
  • composition for forming the photosensitive material used in the present invention may be blended with a variety of blending agents that have been widely known within ranges in which they do not adversely affect the electrophotographic characteristics, such as anti-oxidizing agent, radical trapping agent, singlet quencher, UV-absorbing agent, softening agent, surface reforming agent, defoaming agent, filler, viscosity-imparting agent, dispersion stabilizer, wax, acceptor, donor and the like.
  • blending agents that have been widely known within ranges in which they do not adversely affect the electrophotographic characteristics, such as anti-oxidizing agent, radical trapping agent, singlet quencher, UV-absorbing agent, softening agent, surface reforming agent, defoaming agent, filler, viscosity-imparting agent, dispersion stabilizer, wax, acceptor, donor and the like.
  • a steric hindrance phenolic anti-oxidizing agent is blended in an amount of from 0.1 to 50% by weight per the whole solid component, furthermore, it is allowed to drastically improve the durability of the photosensitive layer without adversely affecting the electrophotographic properties.
  • the electrically conducting substrate for providing a photosensitive layer there can be used a variety of materials having electrically conducting property such as single metals like aluminum, copper, tin, platinum, gold, silver, vanadium, molybdenum, chromium, cadmium, titanium, nickel, indium, stainless steel, brass, plastic materials on which the above-mentioned metals are vaporized or laminated, and glasses coated with aluminum iodide, tin oxide or indium oxide.
  • the shape of the photosensitive material that is used is not limited to only those of the drum type but may be those of the type of belt or sheet.
  • the single-dispersion-layer photosensitive material of the present invention may be employed an aluminum blank tube, preferably an alumite-treated tube having 1 to 50 ⁇ m in thickness of alumite layer on the surface, since there does not develop any interference fringe.
  • the single-dispersion-layer photosensitive material is obtained by blending the charge-generating material, charge-transporting material and binder resin according to a customary method using, for example, roll mill, ball mill, Attritor, paint shaker or an ultrasonic dispersing device, and applying them relying upon a customary application means, followed by drying.
  • the photosensitive layer has a thickness of usually from 10 to 40 ⁇ m and, particularly, from 20 to 35 ⁇ m.
  • organic solvents can be used for obtaining a coating solution.
  • alchols such as methanol, ethanol, isopropanol, butanol, etc.
  • aliphatic hydrocarbons such as n-hexane, octane, cyclohexane, etc.
  • aromatic hydrocarbons such as benzene, toluene, xylene, etc.
  • halogenated hydrocarbons such as dichloromethane, dichloroethane, carbon tetrachloride, chlorobenzene, etc.
  • ethers such as dimethyl ether, diethyl ether, tetrahydrofurane, ethylene glycol dimethyl ether, diethylene glycol dimethyl ether, etc.
  • ketones such as acetone, methyl ethyl ketone, cyclohexanone, etc.
  • esters such as ethyl acetate, methyl acetate, etc., as well as dimethyl
  • the charge-generating agent (CGM) is contained in an amount of from 30 to 90% by weight and, particularly, from 40 to 80% by weight per the solid component in the charge-generating layer (CGL). It is further desired that the charge-transporting agent (CTM) is contained in an amount of from 20 to 70% by weight and, particularly, from 30 to 60% by weight per the solid component in the charge-transporting layer (CTL).
  • the components in the coated layers comply with the components in the single dispersion layer.
  • CGL has a thickness which, usually, lies within a range of from 0.1 to 0.5 ⁇ m and CTL has a thickness which lies within a range of from 5 to 40 ⁇ m and, particularly, from 10 to 25 ⁇ m.
  • CTL has a thickness of from 5 to 40 ⁇ m and, particularly, from 10 to 25 ⁇ m
  • CGL has a thickness of from 0.1 to 0.5 ⁇ m.
  • the present invention can be applied even to an inorganic photosensitive material provided it has surface potential vs. amount of exposure to light characteristics represented by the formula (1).
  • Such an inorganic photosensitive material can be exemplified by an amorphous silicon photosensitive material.
  • amorphous silicon (a-Si) photosensitive layer can be used, such as the one precipitated on an electrically conducting substrate such as an aluminum blank tube by the decomposition of a silane gas with a plasma.
  • This amorphous silicon photosensitive layer may be doped with hydrogen or halogen and, further, with an element of the Group III or the Group V of periodic table, such as boron or phosphorus.
  • the surface layer of the amorphous silicon photosensitive material should exist in the form of a-Si:C. Most desirably, therefore, it is recommended to use a three-layer structure consisting of an a-Si:C surface layer, an a-Si layer and an a-Si:C, B or O barrier layer. It is desired that the amorphous silicon photosensitive layer has a total thickness of from 20 to 100 ⁇ m and, particularly, from 25 to 90 ⁇ m, and the SiC surface layer has a thickness of from 0.2 to 1 ⁇ m and, particularly, from 0.3 to 0.8 ⁇ m. When the lower barrier layer is provided, its thickness may be from 0.5 to 5 ⁇ m and, particularly, from 1 to 3 ⁇ m.
  • a representative amorphous silicon photosensitive material has such physical values as a dark electric conductivity of ⁇ 10-1 ⁇ 1 ⁇ cm ⁇ 1, activation energy of ⁇ 0.85 eV, a photoelectric conductivity of > 10 ⁇ 7 ⁇ 1.cm ⁇ 1, and an optical band gap of from 1.7 to 1.9 eV.
  • the amount of bonded hydrogen is from 10 to 20 atomic %, and the dielectric constant of the film is from 11.5 to 12.5.
  • the photosensitive material may be mainly charged by corona charging using Corotron, Scorotron or the like, or by a widely known contact-type charging device using a charging brush, charging roll or charging blade.
  • the main charging is effected such that the saturation charging potential (VS) is from 400 to 1500 V and, particularly, from 600 to 1200 V.
  • VS saturation charging potential
  • the corona charging therefore, it is desired that a voltage of from 4 to 10 KV is applied to the charger.
  • a voltage which is from 3 to 6 times as great as the charge starting voltage of the photosensitive material is applied to the charging device.
  • the photosensitive material after it is mainly charged is exposed to image-bearing light to form an electrostatic latent image.
  • the source of light for exposure to light may be any source of visible light such as halogen lamp, fluorescent lamp, cold cathode tube, or red or green neon lamp. It is, however, also allowable to use a source of hypochromic light such as red, yellow or green LED. It is further allowed to use a source of laser beam such as semiconductor laser beam.
  • the amount of exposure to light (IB) at a bright portion is such that the residual potential (ER) at the bright portion is lower than the bias potential (EB) and is, more preferably, such that the residual potential (ER) at the bright portion lies within a range defined by the formula (7).
  • the developing is effected by applying a developing bias potential (EB) and, preferably, by applying a potential that satisfies the formula (2) to across the photosensitive material and the developing sleeve, the developing bias potential (EB) having the same polarity as the potential of the photosensitive material and being higher than a potential that corresponds to the point of intersection H (Fig. 2) of a line F approximating the zone of a large amount of exposure to light and a line G approximating the zone of a small amount of exposure to light in the light attenuation characteristics curve of the photosensitive material.
  • EB developing bias potential
  • the developing is effected by the magnetic brush developing.
  • a one-component or a two-component magnetic developing agent is used. This is because, in the present invention, the developing is effected in a state of a potential contrast which is rather lower than that of the conventional method. In this respect, magnetic properties of the toner seriously affect the setting of threshold developing value without fogging.
  • the one-component magnetic developing agent used in the present invention contains a magnetic powder in the toner, and the two-component magnetic developing agent comprises a mixture of a toner and a magnetic carrier.
  • the amount of electric charge possessed by the toner is maintained at a relatively low level.
  • the amount of electric charge of the toner is maintained within a range of from 10 to 30 ⁇ C/g and, particularly, from 15 to 25 ⁇ C/g.
  • the binder resin which is a toner component there can be used a thermoplastic resin, an uncured thermosetting resin, or a thermosetting resin of an initial condensation product.
  • Suitable examples include, in order of suitability, vinyl aromatic resin such as polystyrene, styrene-acrylic copolymer resin, acrylic resin, polyvinyl acetal resin, polyester resin, epoxy resin, phenol resin, petroleum resin, olefin resin and the like.
  • a charge control agent like an oil-soluble dye such as Nigrosine base (CI 50415), oil black (CI 26150), spiron black or the like, or metal complex dye, metal salt of naphthenic acid, metal soap of fatty acid, and salt of resin acid.
  • oil-soluble dye such as Nigrosine base (CI 50415), oil black (CI 26150), spiron black or the like, or metal complex dye, metal salt of naphthenic acid, metal soap of fatty acid, and salt of resin acid.
  • anionic or cationic polar groups there can be exemplified basic nitrogen-containing groups such as primary, secondary or tertiary amino group, quaternary ammonium group, amide group, imino group, imido group, hydrazino group, guanidino group and amidino group.
  • anionic groups there can be exemplified carboxyl group, sulfone group, phosphone group, etc.
  • resins furthermore, there can be exemplified resins obtained by polymerizing a cationic or anionic polar group-containing monomer with other monomers or resins by such means as random copolymerization, block copolymerization or graft copolymerization.
  • the coloring agent to be contained in the resin there can be used the following inorganic or organic pigments and dyes in a single kind or in a combination of two or more kinds, though there is no particular limitation: carbon black such as furnace black or channel black; iron black such as tri-iron tetroxide; rutile or anatase type titanium dioxide; Phthalocyanine Blue; Phthalocyanine Green, cadmium yellow, molybdenum orange; Pyrazolone Red; Fast Violet B; and the like.
  • the above-mentioned coloring agent is used in an amount of from 5 to 20 parts by weight and, particularly, 10 to 15 parts by weight per 100 parts by weight of a fixing resin medium.
  • the above-mentioned resin may contain, as a release agent for thermal fixing, a variety of waxes and low molecular olefin resins.
  • the olefin resins may have a number average molecular weight (Mn) of from 1000 to 10000 and, particularly, from 2000 to 6000.
  • Mn number average molecular weight
  • the olefin resin there can be used polypropylene, polyethylene or propylene-ethylene copolymer. Among them, polypropylene is particularly preferred.
  • magnetic materials to be added to the toner or to be used as a magnetic carrier there can be used widely known magnetic materials such as tri-iron tetroxide (Fe3O4), iron sesquioxide ( ⁇ -Fe2O3), zinc iron oxide (ZnFe2O4), yttrium iron oxide (Y3Fe5O12), cadmium iron oxide (CdFe2O4), gadolinium iron oxide (Gd3Fe5O12), copper ion oxide (CuFe2O4), lead iron oxide (PbFe12O19), nickel iron oxide (NiFe2O4), neodymium iron oxide (NdFeO3), barium iron oxide (BaFe12O19), magnesium iron oxide (MgFe2O4), manganese iron oxide (MnFe2O4), lanthanum iron oxide (LaFeO3), iron powder (Fe), cobalt powder (Co), nickel powder (Ni) and the like. It is desired that these magnetic materials generally
  • the magnetic fine powder is contained in an amount of from 20 to 50% by weight relative to the toner.
  • the magnetic carrier on the other hand, there can be used tri-iron tetroxide, ferrite or iron powder that has been widely known.
  • the magnetic carrier of the ferrite type is particularly suited. It is desired that the magnetic carrier has an average particle diameter of from 60 to 150 ⁇ m, and the magnetic carrier having a particle diameter of not larger than 44 ⁇ m occupies 3 to 15% by weight.
  • the magnetic carrier usually, has a density ⁇ c of from 3.50 to 6.50 g/cm3 and, particularly, from 4.00 to 5.50 g/cm3 though it may vary depending upon the carrier concentration C/D.
  • the saturation magnetization of the carrier is from 30 to 70 emu/g and, particularly, from 53 to 65 emu/g.
  • the magnetic carrier is desirably a ferrite carrier and, particularly, a spherical ferrite carrier satisfying the above-mentioned conditions.
  • the particle size distribution satisfies the above-mentioned conditions but should desirably have a normal distribution or a distribution close thereto.
  • the carrier that is used may not be coated or may be coated with a widely known resin such as silicone resin, acrylic resin, epoxy resin or fluorine-containing resin.
  • the electric resistance of the ferrite carrier varies depending upon its chemical composition but also varies depending upon its particle structure, production method, kind of coating and the thickness.
  • the volume resistivity should be from 5 x 108 to 5 x 1011 ⁇ cm and, particularly, from 1 x 109 to 1 x 1011 ⁇ cm.
  • the weight percentage of the toner T/D in the developing agent is, usually, from 3 to 8% and, particularly, from 3.5 to 7.5%. It is further desired that the developing agent as a whole has an electric resistance of from 1 x 109 to 1 x 1011 ⁇ cm and, particularly, from 5 x 109 to 5 x 1011 ⁇ cm.
  • toner particles having an average particle diameter of from 5 to 15 ⁇ m and, particularly, from 8 to 12 ⁇ m.
  • the particles may have an irregular shape as prepared by the meltkneading method or pulverization method, or may have a spherical shape as prepared by the dispersion or suspension polymerization method.
  • the toner can be produced by any known method such as pulverization-classification method, meltgranulation method, spray-granulation method or polymerization method.
  • the pulverization-classification method is generally employed.
  • the toner components are mixed in advance by a mixer such as Henschel's mixer and are kneaded by using a kneader such as a biaxial extruder.
  • the kneaded composition is then cooled, pulverized and is classified to obtain a toner.
  • an agent to be externally added to the toner furthermore, use is made of magnetic fine particles and hydrophobic silica in combination from the standpoint of preventing fogging on the white paper exposed to light and improving image density.
  • the magnetic fine particles use is made of the above-mentioned magnetic fine particles having a particle diameter of from 0.1 to 0.5 ⁇ m.
  • the magnetic powder which is particularly adapted to this purpose is a fine particulate tri-iron tetroxide (magnetite).
  • the preferred magnetite has an ortho-octahedral shape.
  • the magnetite particles may be treated for their surfaces with a silane coupling agent or a titanium coupling agent. The magnetite particles of which the surfaces are treated with the titanium coupling agent are desirable from the standpoint of resistance against environment.
  • the hydrophobic silica that is externally added is obtained by treating vapor-phase silica, i.e., by treating fine silica obtained by subjecting silicon chloride to a high-temperature (flame) hydrolysis with an organic silicon compound such as silanes like dimethyl dichlorosilane, trimethyl chlorosilane or the like, and by blocking silanol on the surface with organosilane.
  • an organic silicon compound such as silanes like dimethyl dichlorosilane, trimethyl chlorosilane or the like
  • a toner to which an abrasive or a polishing material is externally added can be used for the developing agent of any type.
  • Any known abrasive or polishing material can be used having an average particle diameter of from 0.1 to 5 ⁇ m and, particularly, from 0.15 to 1 ⁇ m. It is desired that these abrasive or polishing material usually has a Mohs' hardness of from 5 to 10.
  • abrasive or the polishing material include oxide ceramics such as alumina (Al2O3), zirconia (ZrO2), mullite (3Al2O3 ⁇ 2SiO2), cordierite (2MgO/2Al2O3/5SiO2), titania (TiO2), steatite (MgO2 ⁇ SiO2), silica, and silica alumina; carbide ceramics such as silicon carbide (SiO2), tungsten carbide (WC), and zirconium carbide (ZrC); nitride ceramics such as boron nitride (BN), titanium nitride (TiN), and silicon nitride (Si3B4); boride ceramics such as zirconium boride (ZrB2) and titanium boride (TiB2); silicate ceramics such as tungsten silicate (WSi2) and molybdenum silicate (Mo
  • the amount of the abrasive or the polishing material added to the toner varies depending upon the kind of the abrasive or the polishing material and cannot be definitely determined. Generally, however, the amount of addition may be selected over a range of from 0.1 to 10% by weight and, particularly, from 0.5 to 5% by weight with respect to the toner, so that optimum scraping amount is obtained. That is, relationships are found between the amount of the toner added and the scraping amount for the abrasives or the polishing materials as shown in Fig. 3, and the amount of blending the abrasive or the polishing material may be so determined that an optimum scraping amount (oxidation degree on the surface of the photosensitive material) is obtained.
  • the toner image is transferred, the paper is separated and the cleaning is effected by using known means under known conditions.
  • the photosensitive material used in Examples was prepared as described below.
  • the following composition for a photosensitive layer was mixed and dispersed in a ball mill for 50 hours to prepare a coating solution for forming a single-layer photosensitive layer.
  • the obtained coating solution was immersion-applied to the surface of an aluminum cylinder having an outer diameter of 78 mm which is an electrically conducting base material, and was dried with the hot air heated at 100 °C for 60 minutes to form a single-layer photosensitive material having a thickness of 25 ⁇ m to obtain a positively charged photosensitive material for electrophotography.
  • Negatively charged toner I Bisazo dye (following formula 12) 10 parts by weight N, N, N', N'-tetrakis (3-methylphenyl)-m-phenylene diamine 100 parts by weight 3,5,3',5'-tetraphenyl-diphenoquinone 50 parts by weight Polycarbonate resin 100 parts by weight Dichloromethane 800 parts by weight
  • composition for a photosensitive layer was mixed and dispersed in a ball mill for 50 hours to prepare a coating solution for generating electric charge.
  • the obtained coating solution was immersion-applied to the surface of an aluminum cylinder having an outer diameter of 78 mm which is an electrically conducting base material, and was dried with the hot air heated at 100 °C for 60 minutes to form a charge-generating layer having a thickness of 0.5 ⁇ m.
  • Bisazo dye (above-mentioned formula 12) 2 parts by weight Polyvinyl butyral resin 1 part by weight Dichloromethane 120 parts by weight
  • the following composition for a photosensitive layer was mixed and dispersed in a ball mill for 24 hours to prepare a coating solution for transporting electric charge.
  • the obtained coating solution was immersion-applied onto the above-mentioned charge-generating layer and was dried with the hot air heated at 90 °C for 60 minutes to form a charge-transporting layer having a thickness of 15 ⁇ m in order to form a laminated-layer photosensitive material.
  • N,N,N',N'-tetrakis (3-methylphenyl)-m-phenylene diamine 80 parts by weight
  • Polycarbonate resin 100 parts by weight Dichloromethane 800 parts by weight
  • the developing agent used in the experiments was prepared as described below.
  • Negatively charged toner I Styrene-acrylic polymer 100 parts by weight Carbon black 6 parts by weight Chromium complex dye (charge control agent) 1 part by weight Low molecular polypropylene (release agent) 2 parts by weight
  • the above-mentioned components were meltkneaded in a biaxial extruder, pulverized in a jet mill, and were subjected to the pneumatic classification using a classifier to obtain toner particles having an average particle diameter of 11 ⁇ m.
  • toner particles and the hydrophobic silica fine particles were mixed and dispersed at a ratio of 0.3% by weight with respect the total amount of the toner to obtain a negatively charged toner I.
  • Styrene-acrylic polymer 100 parts by weight Carbon black 6 parts by weight Chromium complex dye (charge control agent) 1 part by weight Low molecular polypropylene (release agent) 2 parts by weight
  • the above-mentioned components were melt-kneaded in a biaxial extruder, pulverized in a jet mill, and were subjected to the pneumatic classification using a classifier to obtain toner particles having an average particle diameter of 8 ⁇ m.
  • toner particles and the hydrophobic silica fine particles were mixed and dispersed at a ratio of 0.5% by weight with respect to the total amount of the toner to obtain a negatively charged toner II.
  • Positively charged toner III [for OPC] Styrene-acrylic polymer 100 parts by weight Carbon black 9 parts by weight Nigrosine dye (charge control agent) 1 part by weight Low molecular polypropylene (release agent) 2 parts by weight
  • toner particles and the hydrophobic silica fine particles were mixed and dispersed at a ratio of 0.3% by weight with respect the total amount of the toner to obtain a positively charged toner C having an average particle diameter of 10 ⁇ m.
  • Negatively charged toner IV [for a-Si] Styrene-acrylic polymer 100 parts by weight Carbon black 6 parts by weight Chromium complex dye (charge control agent) 1 part by weight Low molecular polypropylene (release agent) 2 parts by weight
  • the above-mentioned components were meltkneaded in a biaxial extruder, pulverized in a jet mill, and were subjected to the pneumatic classification using a classifier to obtain toner particles having an average particle diameter of 10 ⁇ m.
  • toner particles were mixed and dispersed hydrophobic silica fine particles (R972 produced by Japan Aerosil Co.) at a ratio of 0.3% by weight and aluminum oxide (Aluminum Oxide C produced by Japan Aerosil Co.) at a ratio of 0.2% by weight with respect to the total amount of the toner to obtain a negatively charged toner (IV).
  • the negatively charged toners I, IV were blended with a ferrite carrier having an average particle diameter of 100 ⁇ m of which the surfaces were coated with an acrylic resin and a melamine resin, and the negatively charged toner II was blended with a ferrite carrier having an average particle diameter of 80 ⁇ m with stirring to homogeneously mix them together in order to obtain a two-component developing agent having a toner concentration of 3.5%.
  • the positively charged toner III was blended with a ferrite carrier having an average particle size of 80 ⁇ m of which the surfaces were coated with an acrylic resin and a melamine resin with stirring to homogeneously mix them together in order to prepare a two-component developing agent having a toner concentration of 40%.
  • An amorphous silicon (a-Si) photosensitive material (photosensitive material ⁇ ) was also used in addition to the photosensitive material ⁇ (single-layer organic photosensitive material) and photosensitive material ⁇ (laminated-layer organic photosensitive material). That is, the photosensitive material having the same specifications as the a-Si photosensitive material mounted on the electrophotographic copying machine DC-6090 produced by Mita Kogyo Co. was prepared in such a size that can be mounted on a machine modified from the electrophotographic copying machine DC-4556 produced by Mita Kogyo Co.
  • the above-mentioned photosensitive materials ⁇ , ⁇ and ⁇ were mounted on the machine modified from the electrophotographic copying machine DC-4556 produced by Mita Kogyo Co. shown in Figs. 5 and 6, the surface potential at the developing positions was set to be 800 V, and the surface potential was measured while changing the amount of irradiation light.
  • the negatively charged laminated-layer organic photosensitive materials measured by changing the main charging, developing bias, transfer and power transformer of separator shift bias into those of the negative polarity.
  • Table 1 shows the values A to D found in compliance with the aforementioned formula (1) for the photosensitive materials ⁇ , ⁇ and ⁇ , as well as point-of-intersection voltages (EH) found from Fig. 3.
  • photosensitive materials ⁇ , ⁇ and ⁇ were mounted on the machine modified from the electrophotographic copying machine DC-4556 produced by Mita Kogyo Co. shown in Figs. 5 and 6.
  • photosensitive material ⁇ -toner (I), photosensitive material ⁇ -toner (II), photosensitive material ⁇ -toner (III)and photosensitive material ⁇ -toner (IV) as developing agents, images were formed while changing the developing bias potential in order to confirm developing characteristics.
  • a bias potential (absolute value) applied during the developing is set to be higher than a potential (absolute value) that corresponds to an intersecting point of a line approximating the zone of a large amount of exposure to light and a curve approximating the zone of a small amount of exposure to light in the light attenuation characteristics curve of the photosensitive material, in order to entirely utilize the high-sensitivity characteristics in the zone of a small amount of exposure to light and, hence, to form image of a high density without fogging but sacrificing low-sensitivity characteristics in the zone of a large amount of exposure to light to a small degree, i.e., sacrificing a potential drop to a small degree.
  • the bias potential is set to a relatively large value, the amount of exposure to light needs be small and, hence, the source of light needs have a small output, requiring a cooling fan of a small size for removing the heat from the source of light. This makes it possible to decrease the cost of the apparatus and the power cost.
  • the organic photosensitive material needs be irradiated with a small amount of light, the photosensitive material is less deteriorated with light, which is an advantage.
  • the step of exposure to light is accomplished within short periods of time, making it possible to greatly increase the copying speed, printing speed of a facsimile and printing speed of a laser printer.

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Photoreceptors In Electrophotography (AREA)
  • Control Or Security For Electrophotography (AREA)
EP95307715A 1994-10-31 1995-10-30 Entwicklungsvorspannungsauswahl zur Verwendung in einem elektrofotografischem Verfahren, welches fotoempfindliches Material verwendet Expired - Lifetime EP0709747B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP267792/94 1994-10-31
JP26779294 1994-10-31

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EP0709747A2 true EP0709747A2 (de) 1996-05-01
EP0709747A3 EP0709747A3 (de) 1998-04-29
EP0709747B1 EP0709747B1 (de) 2006-03-22

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Publication number Priority date Publication date Assignee Title
CN100357882C (zh) * 2002-01-02 2007-12-26 英特尔公司 处理二进制编码的装置、系统和方法

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US6647230B2 (en) * 2000-09-05 2003-11-11 Canon Kabushiki Kaisha Image-forming apparatus for use with negatively-charged toner and featuring a negatively-chargeable image-bearing member, and process cartridge using same

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JPS6050538A (ja) * 1983-08-31 1985-03-20 Toyo Ink Mfg Co Ltd 電子写真感光体
US4879577A (en) * 1988-04-19 1989-11-07 International Business Machines Corporation Method and apparatus for controlling the electrostatic parameters of an electrophotographic reproduction device
JPH04204876A (ja) * 1990-11-30 1992-07-27 Mita Ind Co Ltd 反転現像制御装置
JP3258681B2 (ja) * 1991-09-06 2002-02-18 株式会社リコー 画像形成装置
JPH06208271A (ja) * 1993-01-12 1994-07-26 Fuji Xerox Co Ltd 画像形成装置

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CN100357882C (zh) * 2002-01-02 2007-12-26 英特尔公司 处理二进制编码的装置、系统和方法

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EP0709747A3 (de) 1998-04-29
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CN1131285A (zh) 1996-09-18
DE69534892T2 (de) 2006-09-07
KR960015100A (ko) 1996-05-22

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