EP4411481A1 - Révélateur d'image à charge électrostatique, cartouche de traitement, appareil de formation d'image et procédé de formation d'image - Google Patents

Révélateur d'image à charge électrostatique, cartouche de traitement, appareil de formation d'image et procédé de formation d'image Download PDF

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Publication number
EP4411481A1
EP4411481A1 EP24158954.8A EP24158954A EP4411481A1 EP 4411481 A1 EP4411481 A1 EP 4411481A1 EP 24158954 A EP24158954 A EP 24158954A EP 4411481 A1 EP4411481 A1 EP 4411481A1
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EP
European Patent Office
Prior art keywords
electrostatic charge
toner
less
image
carrier
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP24158954.8A
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German (de)
English (en)
Inventor
Yasuo Kadokura
Takuro Watanabe
Karin SAKAI
Kazutsuna Sasaki
Yosuke Tsurumi
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Fujifilm Business Innovation Corp
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Fujifilm Business Innovation Corp
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Publication date
Priority claimed from JP2021085621A external-priority patent/JP2022178661A/ja
Application filed by Fujifilm Business Innovation Corp filed Critical Fujifilm Business Innovation Corp
Publication of EP4411481A1 publication Critical patent/EP4411481A1/fr
Pending legal-status Critical Current

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    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00—Developers
    • G03G9/08—Developers with toner particles
    • G03G9/0827—Developers with toner particles characterised by their shape, e.g. degree of sphericity
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00—Developers
    • G03G9/08—Developers with toner particles
    • G03G9/10—Developers with toner particles characterised by carrier particles
    • G03G9/107—Developers with toner particles characterised by carrier particles having magnetic components
    • G03G9/108—Ferrite carrier, e.g. magnetite
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00—Developers
    • G03G9/08—Developers with toner particles
    • G03G9/10—Developers with toner particles characterised by carrier particles
    • G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
    • G03G9/1131—Coating methods; Structure of coatings
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00—Developers
    • G03G9/08—Developers with toner particles
    • G03G9/10—Developers with toner particles characterised by carrier particles
    • G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
    • G03G9/1132—Macromolecular components of coatings
    • G03G9/1133—Macromolecular components of coatings obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00—Developers
    • G03G9/08—Developers with toner particles
    • G03G9/10—Developers with toner particles characterised by carrier particles
    • G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
    • G03G9/1132—Macromolecular components of coatings
    • G03G9/1133—Macromolecular components of coatings obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • G03G9/1134—Macromolecular components of coatings obtained by reactions only involving carbon-to-carbon unsaturated bonds containing fluorine atoms
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00—Developers
    • G03G9/08—Developers with toner particles
    • G03G9/10—Developers with toner particles characterised by carrier particles
    • G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
    • G03G9/1139—Inorganic components of coatings

Definitions

  • the present disclosure relates to an electrostatic charge image developer, a process cartridge, an image forming apparatus, and an image forming method.
  • JP-A-2019-168533 discloses an electrostatic charge image developing toner having a surface property index value of 2.0 or more to 2.8 or less.
  • JP-A-2011-186005 discloses an electrostatic charge image developing carrier including a carrier body having a core material and a coating resin layer, and spherical silica particles having a volume average particle diameter of 50 nm or more and 300 nm or less and adhering to a surface of the carrier body at a ratio of 0.001 parts by mass or more and 0.100 parts by mass or less with respect to 10 parts by mass of the carrier body.
  • JP-A-2008-304745 discloses an electrostatic charge image developer containing a carrier having a resin coating layer on a core material and a toner.
  • the carrier contains 7 to 35% by mass of silica or carbon black in the resin coating layer.
  • a weight average molecular weight of a resin to be coated is 300,000 to 600,000.
  • the toner contains external additive fine particles having a number average particle diameter of 70 nm to 300 nm.
  • An object of the present disclosure is to provide an electrostatic charge image developer including a toner containing a toner particle and an external additive, and a carrier having a magnetic particle and a resin layer.
  • the electrostatic charge image developer prevents occurrence of image omission as compared to an electrostatic charge image developer in which a surface property index value of the toner particle is less than 2.0 or more than 2.8, or an electrostatic charge image developer in which a ratio B/A of a surface area B to a planar view area A is less than 1.020 or more than 1.100, in which the planar view area A and the surface area B are obtained by three-dimensional analysis of the surface of the carrier.
  • an electrostatic charge image developer that prevents occurrence of image omission as compared to the electrostatic charge image developer in which the surface property index value of the toner particle is less than 2.0 or more than 2.8, or an electrostatic charge image developer in which the ratio B/A of the surface area B to the planar view area A is less than 1.020 or more than 1.100, in which the planar view area A and the surface area B are obtained by three-dimensional analysis of the surface of the carrier.
  • an electrostatic charge image developer that prevents the occurrence of image omission as compared to the electrostatic charge image developer in which the surface property index value of the toner particle is less than 2.1 or more than 2.6.
  • an electrostatic charge image developer that prevents the occurrence of image omission as compared to the electrostatic charge image developer in which the ratio B/A of the surface area B to the planar view area A is less than 1.040 or more than 1.080, in which the planar view area A and the surface area B are obtained by three-dimensional analysis of the surface of the carrier.
  • an electrostatic charge image developer that prevents the occurrence of image omission as compared to the electrostatic charge image developer in which the average particle diameter of the inorganic particles contained in the resin layer of the carrier is less than 5 nm or more than 90 nm.
  • an electrostatic charge image developer that prevents the occurrence of image omission as compared to the electrostatic charge image developer in which the average particle diameter of the inorganic particles contained in the resin layer of the carrier is less than 5 nm or more than 70 nm.
  • an electrostatic charge image developer that prevents the occurrence of image omission as compared to the electrostatic charge image developer in which the average thickness of the resin layer of the carrier is less than 0.6 ⁇ m or more than 1.4 ⁇ m.
  • an electrostatic charge image developer that prevents the occurrence of image omission as compared to the electrostatic charge image developer in which the average thickness of the resin layer of the carrier is less than 0.8 ⁇ m or more than 1.2 ⁇ m.
  • an electrostatic charge image developer that prevents the occurrence of image omission as compared to the electrostatic charge image developer in which the storage elastic modulus G' of the toner is less than 6.0 ⁇ 10 8 Pa or more than 1.5 ⁇ 10 9 Pa.
  • an electrostatic charge image developer that prevents the occurrence of image omission as compared to the electrostatic charge image developer in which the storage elastic modulus G' of the toner is less than 8.0 ⁇ 10 8 Pa or more than 1.2 ⁇ 10 9 Pa.
  • an electrostatic charge image developer that prevents the occurrence of image omission as compared to the electrostatic charge image developer in which the silicon element concentration on the carrier surface is 2 atomic% or less or 20 atomic% or more.
  • an electrostatic charge image developer that prevents the occurrence of image omission as compared to the electrostatic charge image developer in which the weight average molecular weight of the resin contained in the resin layer of the carrier is 300,000 or more.
  • a process cartridge that prevents occurrence of image omission as compared to a process cartridge that accommodates the electrostatic charge image developer in which the surface property index value of the toner particle is less than 2.0 or more than 2.8, or an electrostatic charge image developer in which the ratio B/A of the surface area B to the planar view area A is less than 1.020 or more than 1.100, in which the planar view area A and the surface area B are obtained by three-dimensional analysis of the surface of the carrier.
  • an image forming apparatus that prevents occurrence of image omission as compared to an image forming apparatus that accommodates the electrostatic charge image developer in which the surface property index value of toner particle is less than 2.0 or more than 2.8, or the electrostatic charge image developer in which the ratio B/A of the surface area B to the planar view area A is less than 1.020 or more than 1.100, in which the planar view area A and the surface area B are obtained by three-dimensional analysis of the surface of the carrier.
  • an image forming method that prevents occurrence of image omission as compared to an image forming method of accommodating the electrostatic charge image developer in which the surface property index value of toner particle is less than 2.0 or more than 2.8, or the electrostatic charge image developer in which the ratio B/A of the surface area B to the planar view area A is less than 1.020 or more than 1.100, in which the planar view area A and the surface area B are obtained by three-dimensional analysis of the surface of the carrier.
  • a numerical range indicated by “to” indicates a range including numerical values before and after “to” as a minimum value and a maximum value, respectively.
  • an upper limit or a lower limit described in one numerical range may be replaced with an upper limit or a lower limit of a numerical range described in other stages.
  • the upper limit or the lower limit of the numerical range may be replaced with values shown in Examples.
  • step indicates not only an independent step, and even when a step cannot be clearly distinguished from other steps, this step is included in the term “step” as long as an intended purpose of the step is achieved.
  • each component may include plural corresponding substances.
  • the amount of each component in a composition refers to a total amount of the plural substances present in the composition.
  • plural kinds of particles corresponding to each component may be selected.
  • a particle diameter of each component means a value for a mixture of the plural kinds of particles present in the composition.
  • the term "(meth)acryl” means at least one of acryl and methacryl
  • the term “(meth)acrylate” means at least one of acrylate and methacrylate.
  • the term “electrostatic charge image developing toner” is also referred to as a "toner”.
  • the term “electrostatic charge image developing carrier” is also referred to as a “carrier”.
  • the term “electrostatic charge image developer” is also referred to as a "developer”.
  • a developer according to the present exemplary embodiment is a two-component developer including a toner and a carrier.
  • the toner according to the present exemplary embodiment includes a toner particle and an external additive, and a surface property index value of the toner particle is 2.0 or more and 2.8 or less.
  • the surface property index value of the toner particle is an index for evaluating ruggedness of a toner particle surface. As the surface property index value approaches 1.0, the toner particle surface tends to be smooth. As the surface property index value moves away from 1.0, the toner particle surface tends to be rough.
  • the surface property index value of the toner particle is calculated from the following Formulas 1 and 2.
  • the specific surface area measured value of the toner particle is obtained from a nitrogen adsorption amount by BET one-point method (equilibrium relative pressure: 0.3).
  • a flow particle image analysis apparatus FPIA-3000 manufactured by Sysmex Corporation is used for the flow particle image analysis performed to determine the specific surface area calculation value of the toner particle.
  • the FPIA-3000 captures the toner particle, performs two-dimensional image processing, and calculates the equivalent circle diameter from a projection area. Assuming that the toner particle is a true sphere, a surface area and a volume of the true sphere are calculated from the equivalent circle diameter. A sum of the surface areas and a sum of the volumes are calculated from equivalent circle diameters of 4,500 toner particles.
  • Density of the toner particle is measured by measuring true density in accordance with 8.2.2 of JIS K0061: 2001 using a Gulysack type specific gravity bottle.
  • the toner particle to be subjected to the measurement is a particle obtained by removing the external additive from the toner. Removal of the external additive from a surface of the toner is performed by repeating ultrasonic treatment in water containing a surfactant and washing with water.
  • the carrier in the present exemplary embodiment is a resin-coated carrier including a magnetic particle and a resin layer covering the magnetic particle.
  • a ratio B/A of the surface area B to the planar view area A is 1.020 or more and 1.100 or less.
  • the planar view area A and the surface area Bare obtained by three-dimensional analysis of the surface of the carrier.
  • the ratio B/A is an index for evaluating ruggedness of the carrier surface.
  • the ratio B/A is determined by the following method.
  • a scanning electron microscope including four secondary electron detectors for example, electron beam three-dimensional roughness analysis apparatus ERA-8900FE, manufactured by Elionix Inc.
  • ERA-8900FE electron beam three-dimensional roughness analysis apparatus manufactured by Elionix Inc.
  • the surface of one carrier particle is enlarged 5,000 times.
  • a distance between two measurement points is set to 0.06 ⁇ m.
  • the measurement point is set to 400 points in a long side direction and 300 points in a short side direction.
  • a region of 24 ⁇ m ⁇ 18 ⁇ m is measured to obtain three-dimensional image data.
  • a limit wavelength of a spline filter (a frequency selection filter using a spline function) is set to 12 ⁇ m to remove wavelengths having a period of 12 ⁇ m or more. Accordingly, a waviness component of the carrier surface is removed and a roughness component is extracted to obtain a roughness curve.
  • a cutoff value of a Gaussian high-pass filter (a frequency selection filter using a Gaussian function) is set to 2.0 ⁇ m to remove wavelengths having a period of 2.0 ⁇ m or more. Accordingly, wavelengths corresponding to convex portions of the magnetic particle exposed on the carrier surface are removed from the roughness curve after the spline filtering to obtain a roughness curve from which a wavelength component having a period of 2.0 ⁇ m or more is removed.
  • the surface area B ( ⁇ m 2 ) of a region, which is a central portion of 12 ⁇ m ⁇ 12 ⁇ m, (the plan view area A 144 ⁇ m 2 ) is obtained, so as to obtain the ratio B/A.
  • the ratio B/A is calculated for each of 100 carriers and arithmetically averaged.
  • the electrostatic charge image developer according to the present exemplary embodiment prevents occurrence of image omission.
  • a mechanism thereof is presumed as follows.
  • One of causes of the occurrence of the image omission is that the toner remains adhering to a surface of an image carrier and the toner does not move to an intermediate transfer member or a recording medium. Therefore, as one of ways for reducing the occurrence of the image omission, it is possible to prevent the strong adhesion of the toner to the surface of the image carrier. As one of ways for preventing the strong adhesion of the toner to the surface of the image carrier, there is a way in which an appropriate amount of the external additive is present at the toner particle surface.
  • the external additive of the toner moves between the toner and the carrier.
  • an amount of the external additive present at the toner particle surface decreases, and the toner tends to be strongly attached to the surface of the image carrier. This phenomenon is remarkable when image formation having a low image density is repeated.
  • the surface property index value of the toner particle is 2.0 or more, and the ratio B/A of the carrier surface is 1.020 or more. That is, in the developer according to the present exemplary embodiment, a height difference of the ruggedness of the toner particle surface is relatively large, and the number of the ruggedness of the carrier surface is relatively large or the height difference of the ruggedness of the carrier surface is relatively large.
  • the external additive is likely to remain in a concave portion of the toner particle surface, the external additive moves between a convex portion of the toner particle surface and a convex portion of the carrier surface, and the amount of the external additive present in the toner particle surface is maintained in an appropriate range.
  • the surface property index value of the toner particle is less than 2.0, it is presumed that the toner particle surface is excessively flat, a contact surface of the toner particle with respect to the carrier is large, and as a result, a transfer amount of the external additive from the toner to the carrier is large, or the external additive is easily embedded in the toner particle.
  • the ratio B/A of the carrier surface is less than 1.020, it is presumed that the carrier surface is excessively flat, and a contact surface of the carrier with the respect to the toner is large, and as a result, the transfer amount of the external additive from the toner to the carrier is large, or the external additive is easily embedded in the toner particle.
  • the surface property index value of the toner particle is 2.0 or more, and the ratio B/A of the carrier surface is 1.020 or more.
  • the surface property index value of the toner particle is more than 2.8, it is presumed that the height difference of the ruggedness of the toner particle surface is excessively large, the external additive is unevenly distributed in the concave portion of the toner particle, the amount of the external additive in the convex portion of the toner particle decreases, the toner strongly adheres to the surface of the image carrier via the convex portion of the toner particle, and as a result, the image omission occurs.
  • the ratio B/A of the carrier surface is more than 1.100, it is presumed that the number of ruggedness in the carrier surface is excessively large or the height difference of the ruggedness in the carrier surface is excessively large, the amount of the external additive entering the concave portions of the carrier surface is increased, the amount of the external additive returned from the carrier to the toner decreases, the amount of the external additive present in the toner particle surface decreases, and as a result, the image omission occurs.
  • the surface property index value of the toner particle is 2.0 or more and 2.8 or less, preferably 2.1 or more and 2.7 or less, more preferably 2.1 or more and 2.6 or less, still more preferably 2.2 or more and 2.6 or less, and yet still more preferably 2.3 or more and 2.5 or less.
  • the ratio B/A of the carrier surface is 1.020 or more and 1.100 or less, preferably 1.030 or more and 1.090 or less, more preferably 1.040 or more and 1.080 or less, and still more preferably 1.040 or more and 1.070 or less.
  • the surface property index value of the toner particle can be controlled, for example, by adjusting a temperature or pH at the time of fusing and coalescing aggregated particles including the resin particles when the toner particle is produced by an aggregation and coalescence method.
  • the ratio B/A of the carrier surface can be controlled by manufacturing conditions for forming the resin layer. Details will be described later.
  • the toner preferably has a storage elastic modulus G' of 6.0 ⁇ 10 8 Pa or more and 1.5 ⁇ 10 9 Pa or less at a temperature of 30°C in dynamic viscoelasticity measurement.
  • the storage elastic modulus G' means an elastic response component of an elastic modulus in a relationship a stress generated with respect to strain when deformed.
  • the toner tends to be harder as a value of the storage elastic modulus G' is larger.
  • the temperature of 30°C is a temperature at which phase separation between an amorphous polyester resin and a crystalline polyester resin is maintained when the crystalline polyester resin is used.
  • the temperature at which the hardness of the toner is evaluated in the present exemplary embodiment is specified to be 30°C.
  • the storage elastic modulus G' of the toner at a temperature of 30°C is 6.0 ⁇ 10 8 Pa or more, the external additive is less likely to be embedded in the toner particle. As a result, since the external additive is held in the toner particle surface, the toner is prevented from being strongly attached to a photoreceptor, and therefore the image omission is less likely to occur.
  • the storage elastic modulus G' of the toner at the temperature of 30°C is 1.5 ⁇ 10 9 Pa or less, the external additive is less likely to be detached from the toner particle. As a result, since the external additive is held in the toner particle surface, the toner is prevented from being strongly attached to the photoreceptor, and therefore the image omission is less likely to occur.
  • the storage elastic modulus G' of the toner at the temperature of 30°C is more preferably from 7.0 ⁇ 10 8 Pa or more and 1.4 ⁇ 10 9 Pa or less, and still more preferably 8.0 ⁇ 10 8 Pa or more and 1.2 ⁇ 10 9 Pa or less.
  • the storage elastic modulus G' of the toner can be controlled by an amount ratio between the amorphous resin and the crystalline resin contained in the toner.
  • the storage elastic modulus G' of the toner tends to decrease as the amount of the crystalline resin increases.
  • the storage elastic modulus G' of the toner is determined by performing the dynamic viscoelasticity measurement as follows.
  • the toner particle contains, for example, a binder resin, and if necessary, a colorant, a mold releasing agent, and other additives.
  • binder resin examples include vinyl-based resins made of a homopolymer of monomers such as styrenes (such as styrene, parachlorostyrene, and ⁇ -methylstyrene), (meth)acrylates (such as methyl acrylate, ethyl acrylate, n-propyl acrylate, n-butyl acrylate, lauryl acrylate, 2-ethylhexyl acrylate, methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, lauryl methacrylate, and 2-ethylhexyl methacrylate), ethylenically unsaturated nitriles (such as acrylonitrile and methacrylonitrile), vinyl ethers (such as vinyl methyl ether and vinyl isobutyl ether), vinyl ketones (such as vinyl methyl ketone, vinyl ethyl ketone, and vinyl iso
  • binder resin examples include non-vinyl-based resins such as an epoxy resin, a polyester resin, a polyurethane resin, a polyamide resin, a cellulose resin, a polyether resin, and a modified resin, a mixture of the non-vinyl-based resin and the vinyl-based resin, or a graft polymer obtained by polymerizing a vinyl-based monomer in the presence of these non-vinyl-based resins.
  • non-vinyl-based resins such as an epoxy resin, a polyester resin, a polyurethane resin, a polyamide resin, a cellulose resin, a polyether resin, and a modified resin, a mixture of the non-vinyl-based resin and the vinyl-based resin, or a graft polymer obtained by polymerizing a vinyl-based monomer in the presence of these non-vinyl-based resins.
  • binder resins may be used alone or in combination of two or more kinds thereof.
  • the binder resin is suitably a polyester resin.
  • polyester resin examples include a known amorphous polyester resin.
  • the crystalline polyester resin may be used in combination with the amorphous polyester resin.
  • the crystalline polyester resin may be used in a range in which a content thereof is 2 mass% or more and 40 mass% or less (preferably 2 mass% or more and 20 mass% or less) with respect to a total amount of the binder resin.
  • Crystalstalline of a resin means that the resin has a clear endothermic peak rather than a stepwise endothermic change in differential scanning calorimetry (DSC), and specifically means that a half width of the endothermic peak when measured at a heating rate of 10 (°C/min) is within 10°C.
  • amorphous of a resin means that a half width exceeds 10°C, a stepwise change in an endothermic amount is exhibited, or a clear endothermic peak is not observed.
  • amorphous polyester resin examples include a condensed polymer of polycarboxylic acid and polyhydric alcohol.
  • a commercially available product may be used, or a synthetic resin may be used.
  • polycarboxylic acid examples include aliphatic dicarboxylic acids (such as oxalic acid, malonic acid, maleic acid, fumaric acid, citraconic acid, itaconic acid, glutaconic acid, succinic acid, alkenyl succinic acid, adipic acid, and sebacic acid), alicyclic dicarboxylic acids (such as cyclohexanedicarboxylic acid), aromatic dicarboxylic acids (such as terephthalic acid, isophthalic acid, phthalic acid, and naphthalenedicarboxylic acid), anhydrides thereof, and lower (for example, having 1 or more and 5 or less carbon atoms) alkyl esters thereof.
  • the polycarboxylic acid is preferably, for example, an aromatic dicarboxylic acid.
  • a trivalent or higher carboxylic acid having a crosslinked structure or a branched structure may be used in combination with the dicarboxylic acid.
  • the trivalent or higher carboxylic acid include trimellitic acid, pyromellitic acid, anhydrides thereof, and lower (for example, having 1 or more and 5 or less carbon atoms) alkyl esters thereof.
  • the polycarboxylic acid may be used alone or in combination of two or more kinds thereof.
  • polyhydric alcohol examples include aliphatic diols (such as ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, butanediol, hexanediol, and neopentyl glycol), alicyclic diols (such as cyclohexanediol, cyclohexanedimethanol, and hydrogenated bisphenol A), and aromatic diols (such as an ethylene oxide adduct of bisphenol A and a propylene oxide adduct of bisphenol A).
  • the polyhydric alcohol is preferably, for example, an aromatic diol and an alicyclic diol, and more preferably an aromatic diol.
  • a trihydric or higher polyhydric alcohol having a cross-linked structure or a branched structure may be used in combination with a diol.
  • examples of the trihydric or higher polyhydric alcohol include glycerin, trimethylolpropane, and pentaerythritol.
  • the polyhydric alcohol may be used alone or in combination of two or more kinds thereof.
  • a glass transition temperature (Tg) of the amorphous polyester resin is preferably 50°C or higher and 80°C or lower, and more preferably 50°C or higher and 65°C or lower.
  • the glass transition temperature is obtained from a DSC curve obtained by the differential scanning calorimetry (DSC), and is more specifically obtained by an "extrapolated glass transition onset temperature” described in a method for obtaining the glass transition temperature of JIS K 7121:1987 “Method for measuring transition temperature of plastics”.
  • a weight average molecular weight (Mw) of the amorphous polyester resin is preferably 5,000 or more and 1,000,000 or less, and more preferably 7,000 or more and 500,000 or less.
  • a number average molecular weight (Mn) of the amorphous polyester resin is preferably 2,000 or more and 100,000 or less.
  • a molecular weight distribution Mw/Mn of the amorphous polyester resin is preferably 1.5 or more and 100 or less, and more preferably 2 or more and 60 or less.
  • the weight average molecular weight and the number average molecular weight are measured by gel permeation chromatography (GPC).
  • GPC gel permeation chromatography
  • Molecular weight measurement by GPC is performed by using a GPC•HLC-8120GPC manufactured by Tosoh Corporation as a measurement apparatus, using a column TSKgel SuperHM-M (15 cm) manufactured by Tosoh Corporation, and using a THF solvent.
  • the weight average molecular weight and the number average molecular weight are calculated from measurement results using a molecular weight calibration curve prepared using a monodispersed polystyrene standard sample.
  • the amorphous polyester resin is obtained by a known production method. Specifically, for example, the amorphous polyester resin is obtained by a method in which a polymerization temperature is set to 180°C or higher and 230°C or lower, the pressure inside a reaction system is reduced as necessary, and reaction is performed while removing water or alcohols generated during condensation.
  • a solvent having a high boiling point may be added as a dissolution aid to dissolve the monomer.
  • a polycondensation reaction is carried out while distilling off the dissolution aid.
  • the monomer having the poor compatibility may be previously condensed with an acid or alcohol to be polycondensed with the monomer, and then the obtained product may be polycondensed with a main component.
  • Examples of the crystalline polyester resin include a polycondensate of a polycarboxylic acid and a polyhydric alcohol.
  • a commercially available product may be used, or a synthetic resin may be used.
  • the crystalline polyester resin is preferably a polycondensate using a linear aliphatic polymerizable monomer rather than a polymerizable monomer having an aromatic ring.
  • polycarboxylic acid examples include aliphatic dicarboxylic acids (such as oxalic acid, succinic acid, glutaric acid, adipic acid, suberic acid, azelaic acid, sebacic acid, 1,9-nonandicarboxylic acid, 1,10-decandicarboxylic acid, 1,12-dodecanediocarboxylic acid, 1,14 -tetradecanedicarboxylic acid, and 1,18-octadecanedicarboxylic acid), aromatic dicarboxylic acids (such as dibasic acids such as phthalic acid, isophthalic acid, terephthalic acid, and naphthalene-2,6-dicarboxylic acid), anhydrides thereof, and lower (for example, having 1 or more and 5 or less carbon atoms) alkyl esters thereof.
  • aliphatic dicarboxylic acids such as oxalic acid, succinic acid, glutaric acid, adip
  • a trivalent or higher carboxylic acid having a crosslinked structure or a branched structure may be used in combination with the dicarboxylic acid.
  • the trivalent carboxylic acid include aromatic carboxylic acids (such as 1,2,3-benzenetricarboxylic acid, 1,2,4-benzenetricarboxylic acid, and 1,2,4-naphthalenetricarboxylic acid), anhydrides thereof, and lower (for example, having 1 or more and 5 or less carbon atoms) alkyl esters thereof.
  • a dicarboxylic acid having a sulfonic acid group and a dicarboxylic acid having an ethylenic double bond may be used in combination with these dicarboxylic acids.
  • the polycarboxylic acid may be used alone or in combination of two or more kinds thereof.
  • polyhydric alcohol examples include aliphatic diols (such as linear aliphatic diols having 7 or more and 20 or less carbon atoms in the main chain part).
  • aliphatic diol examples include ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,7-heptanediol, 1,8-octanediol, 1,9-nonanediol, 1,10-decanediol, 1,11-undecanediol, 1,12-dodecanediol, 1,13-tridecandiol, 1,14-tetradecanediol, 1,18-octadecanediol, and 1,20-eicosanediol.
  • the aliphatic diol is preferably 1,8-octan
  • a trihydric or higher alcohol having a crosslinked structure or a branched structure may be used in combination with the diol.
  • examples of the trihydric or higher alcohol include glycerin, trimethylolethane, trimethylolpropane, and pentaerythritol.
  • the polyhydric alcohol may be used alone or in combination of two or more kinds thereof.
  • the polyhydric alcohol preferably has an aliphatic diol content of 80 mol% or more, and preferably 90 mol% or more.
  • a melting temperature of the crystalline polyester resin is preferably 50°C or higher and 100°C or lower, more preferably 55°C or higher and 90°C or lower, and still more preferably 60°C or higher and 85°C or lower.
  • the melting temperature is obtained from a DSC curve obtained by the differential scanning calorimetry (DSC) according to the "melting peak temperature” described in a method for obtaining the melting temperature of JIS K7121: 1987 "Method for measuring transition temperature of plastics”.
  • a weight average molecular weight (Mw) of the crystalline polyester resin is preferably 6,000 or more and 35,000 or less.
  • the crystalline polyester resin can be obtained by, for example, a known production method same as the amorphous polyester resin.
  • a content of the binder resin is preferably 40 mass% or more and 95 mass% or less, more preferably 50 mass% or more and 90 mass% or less, and still more preferably 60 mass% or more and 85 mass% or less with respect to a total amount of the toner particle.
  • colorant examples include pigments such as Carbon Black, Chrome Yellow, Hansa Yellow, Benzidine Yellow, Threne Yellow, Quinoline Yellow, Pigment Yellow, Permanent Orange GTR, Pyrazolone Orange, Vulcan Orange, Watchung Red, Permanent Red, Brilliant Carmine 3B, Brilliant Carmine 6B, DuPont Oil Red, Pyrazolone Red, Lithol Red, Rhodamine B Lake, Lake Red C, Pigment Red, Rose Bengal, Aniline Blue, Ultramarine Blue, Calco Oil Blue, Methylene Blue Chloride, Phthalocyanine Blue, Pigment Blue, Phthalocyanine Green, and Malachite Green Oxalate; and acridine dyes, xanthene dyes, azo dyes, benzoquinone dyes, azine dyes, anthraquinone dyes, thioindigo dyes, dioxazine dyes, thiazine dyes, azomethine dyes, indigo dyes, phthalocyanine dyes,
  • the colorant may be used alone or in combination of two or more kinds thereof.
  • a surface-treated colorant may be used as necessary, or the colorant may be used in combination with a dispersant. Plural kinds of colorants may be used in combination.
  • a content of the colorant is preferably 1 mass% or more and 30 mass% or less, and more preferably 3 mass% or more and 15 mass% or less, with respect to the total amount of the toner particle.
  • the mold releasing agent examples include hydrocarbon wax, natural wax such as carnauba wax, rice wax, and candelilla wax, synthetic or mineral/petroleum wax such as montan wax, and ester wax such as fatty acid ester and montanic acid ester.
  • hydrocarbon wax natural wax such as carnauba wax, rice wax, and candelilla wax
  • synthetic or mineral/petroleum wax such as montan wax
  • ester wax such as fatty acid ester and montanic acid ester.
  • the mold releasing agent is not limited thereto.
  • the melting temperature of the mold releasing agent is preferably 50°C or higher and 110°C or lower, and more preferably 60°C or higher and 100°C or lower.
  • the melting temperature is obtained from a DSC curve obtained by the differential scanning calorimetry (DSC) according to the "melting peak temperature” described in a method for obtaining the melting temperature of JIS K7121: 1987 "Method for measuring transition temperature of plastics”.
  • a content of the mold releasing agent is preferably 1 mass% or more and 20 mass% or less, and more preferably 5 mass% or more and 15 mass% or less, with respect to the total amount of the toner particle.
  • additives examples include known additives such as a magnetic body, an electrostatic charge control agent, and an inorganic powder. These additives are contained in the toner particle as internal additives.
  • the toner particle may be a toner particle having a single layer structure, or may be a toner particle having a so-called core-shell structure made of a core portion (core particles) and a coating layer (shell layer) coating the core portion.
  • the toner particle having a core-shell structure may be made of, for example, a core portion made of a binder resin and, if necessary, other additives such as a colorant and a mold releasing agent, and a coating layer made of a binder resin.
  • a volume average particle diameter (D50v) of the toner particle is preferably 2 ⁇ m or more and 10 ⁇ m or less, and more preferably 4 ⁇ m or more and 8 ⁇ m or less.
  • the volume average particle diameter (D50v) of the toner particle is measured using Coulter Multisizer II (manufactured by Beckman Coulter, Inc.) and the electrolytic solution is ISOTON-II (manufactured by Beckman Coulter, Inc.).
  • 0.5 mg or more and 50 mg or less of a measurement sample is added to 2 ml of a 5 mass% aqueous solution of a surfactant (preferably sodium alkylbenzene sulfonate) as a dispersant.
  • a surfactant preferably sodium alkylbenzene sulfonate
  • the obtained mixture is added to 100 ml or more and 150 ml or less of the electrolytic solution.
  • the electrolytic solution in which the sample is suspended is dispersed for 1 minute with an ultrasonic disperser, and the particle size distribution of particles having a particle diameter in a range of 2 ⁇ m or more and 60 ⁇ m or less is measured by the Coulter Multisizer II using an aperture having an aperture diameter of 100 ⁇ m.
  • the number of the particles to be sampled is 50,000.
  • a divided particle size range (channel) is set and a volume-based particle size distribution is obtained. Then, a cumulative distribution is drawn from a small particle diameter side and a particle diameter corresponding to the cumulative percentage of 50% with respect to all the particles is the volume average particle diameter D50v.
  • An average circularity of the toner particle is preferably 0.94 or more and 1.00 or less, and more preferably 0.95 or more and 0.98 or less.
  • the average circularity of the toner particle is obtained by (circle equivalent perimeter)/(perimeter) [(perimeter of a circle having the same projection area as a particle image)/(perimeter of the projected particle image)]. Specifically, the average circularity is a value measured by the following method.
  • the toner particles to be measured are sucked and collected to form a flat flow, and flash light is emitted instantly to capture a particle image as a still image.
  • the average circularity is obtained by a flow-type particle image analysis apparatus (FPIA-3000 manufactured by Sysmex Corporation) that analyzes the particle image.
  • the number of samples for obtaining the average circularity is 4,500.
  • the toner to be measured is dispersed in water containing a surfactant, and then an ultrasonic treatment is performed to obtain toner particle from which the external additive is removed.
  • Examples of the external additive include inorganic particles.
  • Examples of the inorganic particles include SiO 2 , TiO 2 , Al 2 O 3 , CuO, ZnO, SnO 2 , CeO 2 , Fe 2 O 3 , MgO, BaO, CaO, K 2 O, Na 2 O, ZrO 2 , CaO ⁇ SiO 2 , K 2 O ⁇ (TiO 2 ) n , Al 2 O 3 ⁇ 2SiO 2 , CaCO 3 , MgCO 3 , BaSO 4 , and MgSO 4 .
  • the surfaces of the inorganic particles as the external additive are preferably subjected to a hydrophobic treatment.
  • the hydrophobic treatment is performed by, for example, immersing the inorganic particles in a hydrophobic treatment agent.
  • the hydrophobic treatment agent is not particularly limited, and examples thereof include a silane coupling agent, a silicone oil, a titanate coupling agent, and an aluminum coupling agent.
  • the hydrophobic treatment agent may be used alone or in combination of two or more kinds thereof.
  • An amount of the hydrophobic treatment agent is generally, for example, 1 part by mass or more and 10 parts by mass or less with respect to 100 parts by mass of the inorganic particles.
  • Examples of the external additive also include resin particles (resin particles such as polystyrene, polymethylmethacrylate, and melamine resin), and cleaning activators (for example, metal salts of higher fatty acids represented by zinc stearate, and particles of a fluoropolymer).
  • resin particles resin particles such as polystyrene, polymethylmethacrylate, and melamine resin
  • cleaning activators for example, metal salts of higher fatty acids represented by zinc stearate, and particles of a fluoropolymer.
  • An amount of the external additive externally added is, for example, preferably 0.01 mass% or more and 5 mass% or less, and more preferably 0.01 mass% or more and 2.0 mass% or less, with respect to the toner particle.
  • the toner is obtained by preparing toner particle and then externally adding an external additive to the toner particle.
  • the toner particles may be manufactured by either a dry production method (such as a kneading pulverization method) or a wet production method (such as an aggregation and coalescence method, a suspension polymerization method, and a dissolution suspension method). These production methods are not particularly limited, and known production methods are adopted. Among these, it is preferable to obtain the toner particles by the aggregation and coalescence method.
  • a dry production method such as a kneading pulverization method
  • a wet production method such as an aggregation and coalescence method, a suspension polymerization method, and a dissolution suspension method.
  • the toner particles are produced by an aggregation and coalescence method
  • the toner particles are produced through a step of preparing a resin particle dispersion liquid in which resin particles to be a binder resin are dispersed (resin particle dispersion liquid preparation step), a step of aggregating the resin particles (other particles if necessary) in the resin particle dispersion liquid (in a dispersion liquid after mixing with another particle dispersion liquid if necessary) to form aggregated particles (aggregated particle forming step), and a step of heating an aggregated particle dispersion liquid in which the aggregated particles are dispersed and fusing and coalescing the aggregated particles to form the toner particles (fusion and coalescence step).
  • toner particles containing a colorant and a mold releasing agent will be described, but the colorant and the mold releasing agent are used as needed.
  • other additives other than the colorant and the mold releasing agent may be used.
  • a colorant particle dispersion liquid in which colorant particles are dispersed and a mold releasing agent particle dispersion liquid in which mold releasing agent particles are dispersed are prepared.
  • the resin particle dispersion liquid is prepared by, for example, dispersing the resin particles in a dispersion medium with a surfactant.
  • Examples of the dispersion medium used in the resin particle dispersion liquid include an aqueous medium.
  • aqueous medium examples include water such as distilled water and ion-exchanged water, and alcohols. These media may be used alone or in combination of two or more kinds thereof.
  • the surfactant examples include a sulfate-based, sulfonate-based, phosphate-based, soap-based or other anionic surfactant, an amine salt type or quaternary ammonium salt type cationic surfactant, and a polyethylene glycol-based, alkylphenol ethylene oxide adduct-based, or polyhydric alcohol-based nonionic surfactant.
  • anionic surfactant and the cationic surfactant are particularly mentioned.
  • the nonionic surfactant may be used in combination with the anionic surfactant or the cationic surfactant.
  • the surfactant may be used alone or in combination of two or more kinds thereof.
  • Examples of a method for dispersing the resin particles in the dispersion medium in the resin particle dispersion liquid include general dispersion methods such as a rotary shear homogenizer, a ball mill having a medium, a sand mill, and a dyno mill. Depending on a kind of the resin particles, the resin particles may be dispersed in the dispersion medium by a phase inversion emulsification method.
  • phase inversion emulsification method a resin to be dispersed is dissolved in a hydrophobic organic solvent in which the resin is soluble, and a base is added to an organic continuous phase (O phase) to neutralize the resin, and then an aqueous medium (W phase) is added to perform phase inversion from W/O to O/W, and the resin is dispersed in the aqueous medium in the form of particles.
  • O phase organic continuous phase
  • W phase aqueous medium
  • a volume average particle diameter of the resin particles dispersed in the resin particle dispersion liquid is, for example, preferably 0.01 ⁇ m or more and 1 ⁇ m or less, more preferably 0.08 ⁇ m or more and 0.8 ⁇ m or less, and still more preferably 0.1 ⁇ m or more and 0.6 ⁇ m or less.
  • the volume average particle diameter D50v of the resin particles is calculated measured by the volume-based particle size distribution obtained by measurement with a laser diffraction type particle size distribution measuring device (for example, LA-700 manufactured by HORIBA, Ltd.). A divided particle size range is set and the volume-based particle size distribution is obtained. Then, a cumulative distribution is drawn from a small particle diameter side and as a volume average particle diameter D50v, which is a particle diameter corresponding to the cumulative percentage of 50% with respect to all the particles is the volume average particle diameter D50v.
  • the volume average particle diameters of the particles in other dispersion liquid are measured in the same manner.
  • the volume average particle diameters of the particles in another dispersion liquid is measured in the same manner.
  • a content of the resin particles contained in the resin particle dispersion liquid is preferably 5 mass% or more and 50 mass% or less, and more preferably 10 mass% or more and 40 mass% or less.
  • the colorant particle dispersion liquid and the mold releasing agent particle dispersion liquid are also prepared. That is, the volume average particle diameter, dispersion medium, dispersion method, and content of particles of the particles in the resin particle dispersion liquid are the same for the colorant particles dispersed in the colorant particle dispersion liquid and the mold releasing agent particles dispersed in the mold releasing agent particle dispersion liquid.
  • the resin particle dispersion liquid, the colorant particle dispersion liquid, and the mold releasing agent particle dispersion liquid are mixed.
  • the aggregated particles containing the resin particles, the colorant particles, and the mold releasing agent particles having a diameter close to the diameter of the target toner particles are formed by hetero-aggregating the resin particles, the colorant particles, and the release agent particles in the mixed dispersion liquid.
  • the aggregated particles are formed by adding an aggregating agent to the mixed dispersion liquid, adjusting the pH of the mixed dispersion liquid to acidic (for example, a pH of 2 or more and 5 or less), adding a dispersion stabilizer as necessary, then heating the mixed dispersion liquid to a temperature close to the glass transition temperature (specifically, for example, the glass transition temperature of the resin particles -30°C or higher and the glass transition temperature -10°C or lower) of the resin particles, and aggregating the particles dispersed in the mixed dispersion liquid.
  • an aggregating agent for example, adjusting the pH of the mixed dispersion liquid to acidic (for example, a pH of 2 or more and 5 or less), adding a dispersion stabilizer as necessary, then heating the mixed dispersion liquid to a temperature close to the glass transition temperature (specifically, for example, the glass transition temperature of the resin particles -30°C or higher and the glass transition temperature -10°C or lower) of the resin particles, and aggregating the particles dispersed in the mixed
  • the aggregating agent may be added at room temperature (for example, 25°C), the pH of the mixed dispersion liquid may be adjusted to acidic (for example, a pH of 2 or more and 5 or less), the dispersion stabilizer may be added if necessary, and then heating may be performed.
  • the aggregating agent examples include a surfactant having a polarity opposite to that of the surfactant contained in the mixed dispersion liquid, an inorganic metal salt, and a divalent or higher metal complex.
  • a surfactant having a polarity opposite to that of the surfactant contained in the mixed dispersion liquid an inorganic metal salt, and a divalent or higher metal complex.
  • the metal complex is used as the aggregating agent, an amount of the used surfactant is reduced and the chargeability is improved.
  • An additive that forms a complex or a similar bond with metal ions of the aggregating agent may be used together with the aggregating agent, if necessary.
  • the additive is preferably a chelating agent.
  • inorganic metal salt examples include metal salts such as calcium chloride, calcium nitrate, barium chloride, magnesium chloride, zinc chloride, aluminum chloride, and aluminum sulfate, and inorganic metal salt polymers such as polyaluminum chloride, polyaluminum hydroxide, and calcium polysulfide.
  • chelating agent a water-soluble chelating agent may be used.
  • chelating agent include oxycarboxylic acids such as tartaric acid, citric acid, and gluconic acid, and aminocarboxylic acids such as iminodiacetic acid (IDA), nitrilotriacetic acid (NTA), and ethylenediaminetetraacetic acid (EDTA).
  • IDA iminodiacetic acid
  • NTA nitrilotriacetic acid
  • EDTA ethylenediaminetetraacetic acid
  • An addition amount of the chelating agent is preferably 0.01 parts by mass or more and 5.0 parts by mass or less, and more preferably 0.1 parts by mass or more and less than 3.0 parts by mass, with respect to 100 parts by mass of the resin particles.
  • the aggregated particle dispersion liquid in which the aggregated particles are dispersed is heated to, for example, a temperature equal to or higher than the glass transition temperature of the resin particles (for example, a temperature higher than the glass transition temperature of the resin particles by 10°C to 30°C), so that the aggregated particles are fused and coalesced to form the toner particles.
  • a temperature equal to or higher than the glass transition temperature of the resin particles for example, a temperature higher than the glass transition temperature of the resin particles by 10°C to 30°C
  • the toner particles are obtained through the above steps.
  • the toner particles may be produced through a step of obtaining the aggregated particle dispersion liquid in which the aggregated particles are dispersed, then further mixing the aggregated particle dispersion liquid and the resin particle dispersion liquid in which the resin particles are dispersed, and performing aggregation to further adhere and aggregate the resin particles to surfaces of the aggregated particles to form second aggregated particles, and a step of heating a second aggregated particle dispersion liquid in which the second aggregated particles are dispersed to fuse and coalesce the second aggregated particles to form the toner particles having a core-shell structure.
  • the toner particles formed in the solution are subjected to a washing step, a solid-liquid separation step, and a drying step, which are known, to obtain dried toner particles.
  • a washing step from the viewpoint of chargeability, displacement washing with ion-exchanged water may be sufficiently performed.
  • solid-liquid separation step suction filtration, pressure filtration, and the like may be performed from the viewpoint of productivity.
  • the drying step from the viewpoint of productivity, freeze-drying, air-flow drying, fluid-drying, vibration-type fluid-drying, and the like may be performed.
  • the toner is produced by adding the external additive to the toner particles in a dry state and mixing them.
  • the mixing may be carried out by, for example, a V blender, a Henschel mixer, a Loedige mixer, or the like. Further, if necessary, coarse particles in the toner may be removed by using a vibration sieving machine, a wind sieving machine, or the like.
  • the carrier in the present exemplary embodiment includes a magnetic particle and a resin layer covering the magnetic particle.
  • the magnetic particle is not particularly limited, and known magnetic particle used as a core material of the carrier are applied.
  • the magnetic particle includes: a particle of a magnetic metal such as iron, nickel, and cobalt; a particle of a magnetic oxide such as ferrite and magnetite; a resin-impregnated magnetic particle obtained by impregnating a porous magnetic powder with a resin; and a magnetic powder-dispersed resin particle in which a magnetic powder is dispersed and blended in a resin.
  • a ferrite particle is preferred as the magnetic particle in the present exemplary embodiment.
  • a volume average particle diameter of the magnetic particle is preferably 15 ⁇ m or more and 100 ⁇ m or less, more preferably 20 ⁇ m or more and 80 ⁇ m or less, and still more preferably 30 ⁇ m or more and 60 ⁇ m or less.
  • the volume average particle diameter means a particle diameter D50v corresponding to the cumulative percentage of 50% in a volume-based particle size distribution from the side of the small diameter.
  • the arithmetic average height Ra (JIS B0601: 2001) of the roughness curve of the magnetic particle is obtained by observing the magnetic particle at an appropriate magnification (for example, a magnification of 1000 times) using a surface shape measurement apparatus (for example, "Ultra Depth Color 3D shape measurement microscope VK-9700" manufactured by KEYENCE CORPORATION), obtaining a roughness curve at a cutoff value of 0.08 mm, and extracting a reference length of 10 ⁇ m from the roughness curve in a direction of an average line thereof.
  • the arithmetic average value of Ra of 100 magnetic particles is preferably 0.1 ⁇ m or more and 1 ⁇ m or less, and more preferably 0.2 ⁇ m or more and 0.8 ⁇ m or less.
  • saturation magnetization in a magnetic field of 3,000 Oersted is preferably 50 emu/g or more, and more preferably 60 emu/g or more.
  • the saturation magnetization is measured using a vibration sample type magnetic measurement apparatus VSMP10-15 (manufactured by Toei Industry Co., Ltd.).
  • a measurement sample is packed in a cell having an inner diameter of 7 mm and a height of 5 mm and set in the device. The measurement is performed by applying an applied magnetic field and sweeping up to 3000 Oersted. Next, the applied magnetic field is reduced to create a hysteresis curve on recording paper. Saturation magnetization, residual magnetization, and a holding force are obtained from data of the curve.
  • a volume resistivity of the magnetic particle is preferably 1 ⁇ 10 5 ⁇ •cm or more and 1 ⁇ 10 9 ⁇ •cm or less, and more preferably 1 ⁇ 10 7 ⁇ •cm or more and 1 ⁇ 10 9 ⁇ •cm or less.
  • the volume resistivity ( ⁇ •cm) of the magnetic particle is measured as follows.
  • a layer is formed by flatly placing an object to be measured on a surface of a circular jig on which a 20 cm 2 electrode plate is arranged so as to have a thickness of 1 mm or more and 3 mm or less.
  • Another 20 cm 2 electrode plate is placed thereon to sandwich the layer.
  • the thickness (cm) of the layer is measured after applying a load of 4 kg on the electrode plate arranged on the layer. Both electrodes above and below the layer are connected to an electrometer and a high voltage power generator.
  • R represents the volume resistivity ( ⁇ •cm) of the object to be measured
  • E represents the applied voltage (V)
  • I represents the current value (A)
  • I 0 represents a current value (A) under an applied voltage of 0 V
  • L represents the thickness (cm) of the layer.
  • the coefficient 20 represents the area (cm 2 ) of the electrode plate.
  • Examples of a resin constituting the resin layer include: a styrene-acrylic acid copolymer; polyolefin-based resins such as polyethylene and polypropylene; polyvinyl-based or polyvinylidene-based resins such as polystyrene, an acrylic resin, polyacrylonitrile, polyvinyl acetate, polyvinyl alcohol, polyvinyl butyral, polyvinyl chloride, polyvinylcarbazole, polyvinyl ether, and polyvinylketone; a vinyl chloride-vinyl acetate copolymer; straight silicone resins consisting of an organosiloxane bond or a modified product thereof; fluororesins such as polytetrafluoroethylene, polyvinyl fluoride, polyvinylidene fluoride, and polychlorotrifluoroethylene; polyester, polyurethane; polycarbonate; amino resins such as urea and formaldehyde resins; and epoxy resins
  • the resin layer preferably contains an acrylic resin having an alicyclic.
  • a polymerization component of the acrylic resin having the alicyclic is preferably a lower alkyl ester of (meth)acrylic acid (for example, (meth)acrylic acid alkyl ester having an alkyl group having 1 or more and 9 or less carbon atoms), and specific examples thereof include methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, butyl (meth)acrylate, hexyl (meth)acrylate, cyclohexyl (meth)acrylate, and 2-ethylhexyl (meth)acrylate. These monomers may be used alone or in combination of two or more kinds thereof.
  • the acrylic resin having the alicyclic preferably contains cyclohexyl (meth) acrylate as the polymerization component.
  • a content of a monomer unit derived from the cyclohexyl (meth) acrylate contained in the acrylic resin having the alicyclic is preferably 75 mass% or more and 100 mass% or less, more preferably 85 mass% or more and 100 mass% or less, and still more preferably 95 mass% or more and 100 mass% or less, with respect to a total mass of the acrylic resin having the alicyclic.
  • the weight average molecular weight of the resin contained in the resin layer is preferably less than 300,000.
  • a strength of the resin layer is higher than that when the weight average molecular weight of the resin is 300,000 or more, and the resin layer is less likely to be peeled off when image formation is repeated. Therefore, it is presumed that mechanical stress of the carrier with respect to the toner is prevented from being increased, the external additive is prevented from being embedded in the toner particles, and the occurrence of the image omission is prevented.
  • the weight average molecular weight of the resin contained in the resin layer is preferably 50,000 or more and less than 300,000, more preferably 100,000 or more and 250,000 or less, and still more preferably 100,000 or more and 200,000 or less.
  • the weight average molecular weight of the acrylic resin having the alicyclic contained in the resin layer is preferably 50,000 or more and less than 300,000, more preferably 100,000 or more and 250,000 or less, and still more preferably 100,000 or more and 200,000 or less.
  • the weight average molecular weight of the resin contained in the resin layer is a weighted average obtained by weighting the weight average molecular weight of each resin by a content ratio (on a mass basis) of each resin.
  • the weight average molecular weight of the resin contained in the resin layer is measured by gel permeation chromatography (GPC).
  • GPC gel permeation chromatography
  • GPC • HLC-8120GPC manufactured by Tosoh Corporation is used as a measurement apparatus
  • column TSKgel Super HM-M (15 cm) manufactured by Tosoh Corporation is used, and tetrahydrofuran is used as a solvent.
  • the weight average molecular weight is calculated from a measurement result using a molecular weight calibration curve prepared using a monodispersed polystyrene standard sample.
  • the resin layer preferably contains inorganic particles.
  • the carbon black is not treated as an inorganic particle in the resin layer of the carrier.
  • the inorganic particles When the inorganic particles are contained in the resin layer, a form in which fine ruggedness is appropriately present in the carrier surface is formed. Most of the ruggedness are covered with the resin, but some the inorganic particles may be exposed. Since the exposed inorganic particles are not charged by contact with the toner unlike the resin, excessive charging of the carrier surface can be reduced. Further, when the resin layer of the carrier is abraded by repeating the image formation, the ruggedness is selectively abraded, and a part of the inorganic particles in the resin layer is newly exposed.
  • Examples of the inorganic particles contained in the resin layer include metal oxide particles such as silica, titanium oxide, zinc oxide, and tin oxide, metal compound particles such as barium sulfate, aluminum borate, and potassium titanate, and metal particles such as gold, silver, and copper.
  • metal oxide particles such as silica, titanium oxide, zinc oxide, and tin oxide
  • metal compound particles such as barium sulfate, aluminum borate, and potassium titanate
  • metal particles such as gold, silver, and copper.
  • the silica particles are preferable.
  • Surfaces of the inorganic particles may be subjected to a hydrophobic treatment.
  • a hydrophobic treatment agent include known organic silicon compounds having an alkyl group (for example, a methyl group, an ethyl group, a propyl group, a butyl group, and the like), and specific examples thereof include an alkoxysilane compound, a siloxane compound, and a silazane compound.
  • the hydrophobic treatment agent is preferably a silazane compound, and preferably hexamethyldisilazane.
  • the hydrophobic treatment agent may be used alone or in combination of two or more kinds thereof.
  • Examples of a method for hydrophobizing the inorganic particles with the hydrophobic treatment agent include a method in which supercritical carbon dioxide is used and the hydrophobic treatment agent is dissolved in the supercritical carbon dioxide to be attached to the surfaces of the inorganic particles, a method in which a solution containing a hydrophobic treatment agent and a solvent for dissolving the hydrophobic treatment agent is applied (for example, sprayed or coated) to the surfaces of the inorganic particles in the atmosphere to attach the hydrophobic treatment agent to the surfaces of the inorganic particles, and a method in which a solution containing a hydrophobic treatment agent and a solvent for dissolving the hydrophobic treatment agent is added to and held in an inorganic particle dispersion liquid in the air, and then a mixed solution of the inorganic particle dispersion liquid and the solution is dried.
  • An average particle diameter of the inorganic particles contained in the resin layer is preferably 5 nm or more and 90 nm or less.
  • the average particle diameter of the inorganic particles in the resin layer is 5 nm or more, a filler effect of increasing the strength of the resin layer is easily obtained, and the resin layer is less likely to be peeled off when the image formation is repeated.
  • the average particle diameter of the inorganic particles in the resin layer is 90 nm or less, the inorganic particles are less likely to be detached from the convex portion of the resin layer, and the resin layer is less likely to be peeled off when the image formation is repeated. In either case, it is presumed that mechanical stress of the carrier with respect to the toner is prevented from being increased, the external additive is prevented from being embedded in the toner particles, and the occurrence of the image omission is prevented.
  • the average particle diameter of the inorganic particles in the resin layer is more preferably 5 nm or more and 70 nm or less, still more preferably 5 nm or more and 50 nm or less, and yet still more preferably 8 nm or more and 50 nm or less.
  • the average particle diameter of the inorganic particles contained in the resin layer can be controlled by a size of the inorganic particles used for forming the resin layer.
  • An average thickness of the resin layer is preferably 0.6 ⁇ m or more and 1.4 ⁇ m or less.
  • the resin layer When the average thickness of the resin layer is 0.6 ⁇ m or more, the resin layer is less likely to be peeled off when the image formation is repeated. When the average thickness of the resin layer is 1.4 ⁇ m or less, the toner external additive is less likely to adhere to or be embedded in the resin layer after the toner external additive is transferred to the resin layer, and the transfer amount of the external additive from the toner to the carrier does not become excessive. In either case, as a result, it is presumed that the occurrence of the image omission is prevented.
  • the average thickness of the resin layer is more preferably 0.8 ⁇ m or more and 1.2 ⁇ m or less, and still more preferably 0.8 ⁇ m or more and 1.1 ⁇ m or less.
  • the average thickness of the resin layer can be controlled by an amount of the resin used for forming the resin layer, and the average thickness of the resin layer increases as the amount of the resin with respect to the amount of the magnetic particle increases.
  • the average particle diameter of the inorganic particles contained in the resin layer and the average thickness of the resin layer are determined by the following methods.
  • the carrier is embedded in an epoxy resin and cut with a microtome to prepare a carrier cross section.
  • a scanning electron microscope (SEM) image obtained by capturing the carrier cross section with the SEM is taken into an image processing analyzer for image analysis.
  • 100 inorganic particles (primary particles) in the resin layer are randomly selected, and an equivalent circular diameter (nm) of each particle is calculated and arithmetically averaged to obtain the average particle diameter (nm) of the inorganic particles.
  • the thickness ( ⁇ m) of the resin layer is measured by randomly selecting 10 points per particle of the carrier, and 100 particles of the carrier are further selected to measure thicknesses thereof, and all the thicknesses are arithmetically averaged to obtain the average thickness ( ⁇ m) of the resin layer.
  • the resin layer of the carrier preferably contains the silica particles, and a silicon element concentration at the carrier surface determined by an X-ray photoelectron spectroscopy is more than 2 atomic% and less than 20 atomic%.
  • the silicon element concentration is more than 2 atomic%, it means that the silica particles are appropriately distributed at the resin layer surface. Therefore, the chargeability of the carrier surface is appropriately lowered.
  • the silicon element concentration is less than 20 atomic%, it means that an amount of silica particles distributed at the resin layer surface is not too large. Therefore, the chargeability of the carrier surface is not excessively lowered.
  • the silicon element concentration is more preferably more than 5 atomic% and less than 20 atomic%, and still more preferably more than 6 atomic% and less than 19 atomic%.
  • the silicon element concentration at the carrier surface can be controlled by the amount of the silica particles used for forming the resin layer, and the silicon element concentration at the carrier surface increases as the amount of the silica particles with respect to the amount of the resin increases.
  • the silicon element concentration (atomic%) of the carrier surface is determined based on a peak intensity of each element by analyzing the carrier as a sample by the X-ray photoelectron spectroscopy (XPS) under the following conditions.
  • XPS X-ray photoelectron spectroscopy
  • a content of the inorganic particles contained in the resin layer is preferably 10 mass% or more and 60 mass% or less, more preferably 15 mass% or more and 55 mass% or less, and still more preferably 20 mass% or more and 50 mass% or less with respect to a total mass of the resin layer.
  • a content of the silica particles contained in the resin layer is preferably 10 mass% or more and 60 mass% or less, more preferably 15 mass% or more and 55 mass% or less, and still more preferably 20 mass% or more and 50 mass% or less with respect to a total mass of the resin layer.
  • the resin layer may contain conductive particles for a purpose of controlling charging and resistance.
  • conductive particles include carbon black and conductive particles among the above-mentioned inorganic particles.
  • Examples of a method for forming the resin layer on surfaces of the magnetic particle include a wet production method and a dry production method.
  • the wet production method is a production method using a solvent that dissolves or disperses the resin constituting the resin layer.
  • the dry production method is a production method that does not use the above solvent.
  • Examples of the wet production method include an immersion method in which the magnetic particles are immersed in a resin liquid for forming the resin layer to be coated, a spray method in which a resin liquid for forming the resin layer is sprayed on the surfaces of the magnetic particles, a fluidized bed method in which a resin liquid for forming the resin layer is sprayed while the magnetic particles are in a state of being fluidized in a fluidized bed, and a kneader coater method in which the magnetic particles and a resin liquid for forming the resin layer are mixed in a kneader coater to remove a solvent. These production methods may be repeated or combined.
  • the resin liquid for forming the resin layer used in the wet production method is prepared by dissolving or dispersing a resin, inorganic particles, and other components in a solvent.
  • the solvent is not particularly limited, and for example, aromatic hydrocarbons such as toluene and xylene, ketones such as acetone and methyl ethyl ketone, ethers such as tetrahydrofuran and dioxane, and the like may be used.
  • Examples of the dry production method include a method of forming the resin layer by heating a mixture of the magnetic particles and a resin for forming the resin layer in a dry state. Specifically, for example, the magnetic particles and the resin for forming the resin layer are mixed in a gas phase and heated and melted to form the resin layer.
  • the ratio B/A can be controlled by production conditions.
  • the ratio B/A is controlled by adjusting a mixing time between particles to be coated and a resin liquid for forming the resin layer.
  • the ratio B/A is controlled by adjusting the particle diameter and the content of the inorganic particles contained in the liquid composition or an amount of the liquid composition applied to the resin-coated carrier.
  • An exposed area ratio of the magnetic particle at the carrier surface is preferably 5% or more and 30% or less, more preferably 7% or more and 25% or less, and still more preferably 10% or more and 25% or less.
  • the exposed area ratio of the magnetic particle in the carrier can be controlled by the amount of the resin used for forming the resin layer, and the exposed area ratio becomes smaller as the amount of the resin relative to the amount of the magnetic particle increases.
  • the exposed area ratio of the magnetic particle at the carrier surface is a value obtained by the following method.
  • a target carrier and magnetic particle obtained by removing the resin layer from the target carrier are prepared.
  • Examples of a method for removing the resin layer from the carrier include a method of dissolving a resin component with an organic solvent to remove the resin layer and a method of removing the resin component by heating at about 800°C to remove the resin layer.
  • the carrier and the magnetic particle are used as measurement samples, and Fe concentrations (atomic%) at surfaces of the samples are quantified by XPS, and (Fe concentration of the carrier)/(Fe concentration of the magnetic particle) ⁇ 100 is calculated and used as the exposed area ratio (%) of the magnetic particle.
  • a volume average particle diameter of the carrier is preferably 10 ⁇ m or more and 120 ⁇ m or less, more preferably 20 ⁇ m or more and 100 ⁇ m or less, and still more preferably 30 ⁇ m or more and 80 ⁇ m or less.
  • the volume average particle diameter means a particle diameter D50v corresponding to the cumulative percentage of 50% in a volume-based particle size distribution drawn from the side of the small diameter.
  • An image forming apparatus includes: an image carrier; a charging unit that charges a surface of the image carrier; an electrostatic charge image forming unit that forms an electrostatic charge image on the surface of the image carrier charged; a developing unit that accommodates an electrostatic charge image developer and develops, by the electrostatic charge image developer, an electrostatic charge image formed on the surface of the image carrier as a toner image; a transfer unit that transfers the toner image formed on the surface of the image carrier to a surface of a recording medium; and a fixing unit that fixes the toner image transferred to the surface of the recording medium.
  • the electrostatic charge image developer the electrostatic charge image developer according to the present exemplary embodiment is applied.
  • an image forming method (an image forming method according to the present exemplary embodiment) including a charging step of charging the surface of the image carrier; an electrostatic charge image forming step of forming the electrostatic charge image on the surface of the image carrier charged; a developing step of developing, by the electrostatic charge image developer according to the present exemplary embodiment, the electrostatic charge image formed on the surface of the image carrier as the toner image; a transfer step of transferring the toner image formed on the surface of the image carrier to the surface of the recording medium; and a fixing step of fixing the toner image transferred to the surface of the recording medium is performed.
  • a known image forming apparatus such as a direct transfer type apparatus that directly transfers the toner image formed on the surface of the image carrier to the recording medium, an intermediate transfer type apparatus that primarily transfers the toner image formed on the surface of the image carrier to a surface of an intermediate transfer body, and secondarily transfers the toner image transferred to the surface of the intermediate transfer body to the surface of the recording medium, an apparatus provided with a cleaning unit for cleaning the surface of the image carrier after the transfer of the toner image and before charging, and an apparatus provided with a discharging unit for discharging the surface of the image carrier by irradiation with discharging light after the transfer of the toner image and before the charging, is applied to the image forming apparatus according to the present exemplary embodiment.
  • the transfer unit includes, for example, an intermediate transfer body on which a toner image is transferred onto a surface thereof, a primary transfer unit that primarily transfers the toner image formed on the surface of the image carrier onto the surface of the intermediate transfer body, and a secondary transfer unit that secondarily transfers the toner image transferred on the surface of the intermediate transfer body onto the surface of the recording medium.
  • a part including the developing unit may have a cartridge structure (process cartridge) attached to and detached from the image forming apparatus.
  • a process cartridge for example, a process cartridge that accommodates the electrostatic charge image developer according to the present exemplary embodiment and provided with a developing unit is preferably used.
  • Fig. 1 is a schematic configuration diagram illustrating the image forming apparatus according to the present exemplary embodiment.
  • the image forming apparatus illustrated in Fig. 1 includes first to fourth electrophotographic image forming units 10Y, 10M, 10C, and 10K (image forming units) that output images of respective colors of yellow (Y), magenta (M), cyan (C), and black (K) based on image data subjected to color separation.
  • image forming units hereinafter may be simply referred to as "unit" 10Y, 10M, 10C, and 10K are arranged side by side at a predetermined distance from each other in a horizontal direction.
  • These units 10Y, 10M, 10C, and 10K may be process cartridges that are attached to and detached from the image forming apparatus.
  • an intermediate transfer belt (an example of the intermediate transfer body) 20 extends through respective units.
  • the intermediate transfer belt 20 is provided by being wound around a drive roller 22 and a support roller 24, and travels in a direction from the first unit 10Y to the fourth unit 10K.
  • a force is applied to the support roller 24 in a direction away from the drive roller 22 by a spring or the like (not shown), and tension is applied to the intermediate transfer belt 20 wound around the drive roller 22 and the support roller 24.
  • An intermediate transfer body cleaning device 30 is provided on a side surface of an image carrier of the intermediate transfer belt 20 so as to face the drive roller 22.
  • Yellow, magenta, cyan, and black toners contained in toner cartridges 8Y, 8M, 8C, and 8K are supplied to developing devices 4Y, 4M, 4C, and 4K (an example of the developing unit) of the units 10Y, 10M, 10C, and 10K, respectively.
  • the first to fourth units 10Y, 10M, 10C, and 10K have the same configuration and operation, here, the first unit 10Y, which is arranged on an upstream side in a travelling direction of the intermediate transfer belt and forms a yellow image, will be described as a representative.
  • 1M, 1C, and 1K in the second to fourth units 10M, 10C, and 10K are photoconductors corresponding to a photoconductor 1Y in the first unit 10Y; 2M, 2C and 2K are charging rollers corresponding to a charging roller 2Y; 3M, 3C, and 3K are laser beams corresponding to a laser beam 3Y; and 6M, 6C, and 6K are photoconductor cleaning devices corresponding to a photoconductor cleaning device 6Y.
  • the first unit 10Y includes the photoconductor 1Y that acts as an image carrier.
  • the charging roller an example of the charging unit 2Y that charges a surface of the photoconductor 1Y to a predetermined potential
  • an exposure device an example of the electrostatic charge image forming unit 3 that exposes the charged surface with the laser beam 3Y based on a color-separated image signal to form an electrostatic charge image
  • the developing device an example of the developing unit
  • 4Y that supplies a charged toner to the electrostatic charge image to develop the electrostatic charge image
  • a primary transfer roller 5Y an example of the primary transfer unit
  • the photoconductor cleaning device an example of the cleaning unit 6Y that removes the toner remaining on the surface of the photoconductor 1Y after the primary transfer.
  • the primary transfer roller 5Y is arranged on an inner side of the intermediate transfer belt 20 and is provided at a position facing the photoconductor 1Y.
  • a bias power supply (not shown) that applies a primary transfer bias is connected to each of the primary transfer rollers 5Y, 5M, 5C, and 5K of respective units. Each bias power supply changes a value of the transfer bias applied to each primary transfer roller under the control of a controller (not shown).
  • the surface of the photoconductor 1Y is charged to a potential of -600 V to -800 V by using the charging roller 2Y
  • the photoconductor 1Y is formed by laminating a photoconductive layer on a conductive substrate (for example, having a volume resistivity of 1 ⁇ 10 -6 ⁇ •cm or less at 20°C).
  • the photoconductive layer usually has high resistance (resistance of general resin), but has a property that when irradiated with a laser beam, the specific resistance of the portion irradiated with the laser beam changes. Therefore, the charged surface of the photoconductor 1Y is irradiated with the laser beam 3Y from the exposure device 3 in accordance with yellow image data sent from the controller (not shown). As a result, an electrostatic charge image having a yellow image pattern is formed on the surface of the photoconductor 1Y
  • the electrostatic charge image is an image formed on the surface of the photoconductor 1Y by charging, and is a so-called negative latent image formed by lowering the specific resistance of the portion of the photoconductive layer irradiated with the laser beam 3Y to flow charges charged on the surface of the photoconductor 1Y and by, on the other hand, leaving charges of a portion not irradiated with the laser beam 3Y
  • the electrostatic charge image formed on the photoconductor 1Y rotates to a predetermined developing position as travelling of the photoconductor 1Y Then, at this developing position, the electrostatic charge image on the photoconductor 1Y is developed and visualized as a toner image by the developing device 4Y
  • an electrostatic charge image developer containing at least a yellow toner and a carrier is accommodated.
  • the yellow toner is triboelectrically charged by being stirred inside the developing device 4Y, and has charges of the same polarity (negative polarity) as the charges charged on the photoconductor 1Y and is held on a developer roller (an example of a developer holder). Then, when the surface of the photoconductor 1Y passes through the developing device 4Y, the yellow toner electrostatically adheres to a discharged latent image portion on the surface of the photoconductor 1Y, and the latent image is developed by the yellow toner.
  • the photoreceptor 1Y on which the yellow toner image is formed continuously travels at a predetermined speed, and the toner image developed on the photoconductor 1Y is conveyed to a predetermined primary transfer position.
  • a primary transfer bias is applied to the primary transfer roller 5Y, an electrostatic force from the photoconductor 1Y to the primary transfer roller 5Y acts on the toner image, and the toner image on the photoconductor 1Y is transferred onto the intermediate transfer belt 20.
  • the transfer bias applied at this time has a polarity (+) opposite to the polarity (-) of the toner, and is controlled to, for example, +10 ⁇ A by the controller (not shown) in the first unit 10Y.
  • the toner remaining on the photoconductor 1Y is removed and collected by the photoconductor cleaning device 6Y.
  • the primary transfer biases applied to the primary transfer rollers 5M, 5C, and 5K of the second unit 10M and the subsequent units are also controlled in the same manner as in the first unit.
  • the intermediate transfer belt 20 to which the yellow toner image is transferred by the first unit 10Y is sequentially conveyed through the second to fourth units 10M, 10C, and 10K, and toner images of the respective colors are superimposed and transferred in a multiple manner.
  • the intermediate transfer belt 20 onto which the toner images of four colors are transferred in a multiple manner through the first to fourth units arrives at a secondary transfer unit including the intermediate transfer belt 20, the support roller 24 in contact with an inner surface of the intermediate transfer belt, and a secondary transfer roller (an example of a secondary transfer unit) 26 arranged on an image holding surface side of the intermediate transfer belt 20.
  • a recording paper (an example of the recording medium) P is fed through a supply mechanism into a gap where the secondary transfer roller 26 and the intermediate transfer belt 20 are in contact with each other at a predetermined timing, and a secondary transfer bias is applied to the support roller 24.
  • the transfer bias applied at this time has the same polarity (-) as the polarity (-) of the toner.
  • the secondary transfer bias at this time is determined according to the resistance detected by a resistance detecting unit (not shown) that detects the resistance of the secondary transfer unit, and is subjected to voltage control.
  • the recording paper P is sent to a pressure contact portion (nip portion) of a pair of fixing rollers in a fixing device 28 (an example of the fixing unit), and the toner image is fixed onto the recording paper P, thereby forming a fixed image.
  • Examples of the recording paper P onto which the toner image is transferred include plain paper used in electrophotographic copiers and printers.
  • As the recording medium in addition to the recording paper P, an OHP sheet or the like may be used.
  • the surface of the recording paper P is also preferably smooth.
  • coated paper obtained by coating the surface of the plain paper with a resin or the like, art paper for printing, or the like is preferably used.
  • the recording paper P, on which the fixing of the color image is completed, is conveyed out toward a discharge unit, and a series of color image forming operations is completed.
  • the process cartridge according to the present exemplary embodiment includes a developing unit that accommodates the electrostatic charge image developer according to the present exemplary embodiment and develops, by the electrostatic charge image developer, the electrostatic charge image formed on the surface of the image carrier as the toner image, and is attached to and detached from the image forming apparatus.
  • the process cartridge according to the present exemplary embodiment is not limited to the above configuration and may be configured to include a developing unit and, if necessary, at least one selected from other units such as an image carrier, a charging unit, an electrostatic charge image forming unit, and a transfer unit.
  • Fig. 2 is a schematic configuration diagram illustrating the process cartridge according to the present exemplary embodiment.
  • a process cartridge 200 shown in Fig. 2 is formed as a cartridge by, for example, integrally combining and holding a photoconductor 107 (an example of the image carrier), a charging roller 108 (an example of the charging unit), an image developing device 111 (an example of the developing unit), and a photoconductor cleaning device 113 (an example of a cleaning unit) provided around the photoconductor 107 by a housing 117 provided with a mounting rail 116 and an opening 118 for exposure.
  • 109 denotes an exposure device (an example of the electrostatic charge image forming unit)
  • 112 denotes a transfer device (an example of the transfer unit)
  • 115 denotes a fixing device (an example of the fixing unit)
  • 300 denotes recording paper (an example of the recording medium).
  • Synthesis, treatment, production, and the like are performed at a room temperature (25°C ⁇ 3°C), unless otherwise specified.
  • a flask equipped with a stirrer, a nitrogen inlet tube, a temperature sensor, and a rectifying column is charged with the above materials, a temperature is raised to 220°C over 1 hour, and 1 part of titanium tetraethoxide is added to 100 parts of the above materials.
  • the temperature is increased to 230°C over 30 minutes while distilling off generated water, and a dehydration condensation reaction is continued at the temperature for 1 hour, and then a reaction product is cooled to obtain an amorphous polyester resin (1) (weight average molecular weight: 18,000, glass transition temperature: 59°C).
  • amorphous polyester resin (1) 40 parts of ethyl acetate and 25 parts of 2-butanol are added into a vessel equipped with a temperature control unit and a nitrogen substitution unit to prepare a mixed solvent, and then 100 parts of the amorphous polyester resin (1) is gradually put into the vessel and dissolved.
  • a 10% ammonia aqueous solution (corresponding to 3 times of an acid value of the resin in terms of a molar ratio) is added thereto and stirred for 30 minutes.
  • an inside of the vessel is replaced with dry nitrogen, the temperature is maintained at 40°C, and 400 parts of ion-exchanged water is added dropwise while stirring a mixed solution to perform emulsification.
  • an emulsion is returned to 25°C to obtain a resin particle dispersion liquid in which resin particles having the volume average particle diameter of 180 nm are dispersed.
  • Ion exchange water is added to the resin particle dispersion liquid to adjust a solid content to 20%, thereby obtaining an amorphous polyester resin dispersion liquid (1).
  • the above materials are charged into a flask and raised to a temperature of 160°C over 1 hour, and after confirming that the inside of the reaction system is uniformly stirred, 0.03 parts of dibutyltin oxide is added. The temperature is raised to 200°C over 6 hours while water to be produced is distilled off, and stirring is continued at 200°C for 4 hours. Next, a reaction liquid is cooled to perform solid-liquid separation, and a solid is dried under a reduced pressure at a temperature of 40°C to obtain a crystalline polyester resin (1) (weight average molecular weight: 15,000, melting point: 64°C).
  • crystalline polyester resin (1) 50 parts of the crystalline polyester resin (1), 2 parts of an anionic surfactant (NEOGEN RK, manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd.), and 200 parts of the ion exchange water are mixed and heated to 120°C, sufficiently dispersed by a homogenizer (ULTRA-TURRAX T50 manufactured by IKA Co., Ltd.), and then subjected to a dispersion treatment with a pressure discharge type homogenizer. When the volume average particle diameter reaches 180 nm, the mixture is recovered to obtain a crystalline polyester resin dispersion liquid (1) having a solid content of 20%.
  • an anionic surfactant NEOGEN RK, manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd.
  • ULTRA-TURRAX T50 manufactured by IKA Co., Ltd.
  • the above materials are mixed and subjected to a dispersion treatment for 60 minutes using a high-pressure impact type disperser (ULTIMAIZER HJP30006 manufactured by Sugino Machine Limited) to obtain a colorant dispersion liquid (C1) having a solid content of 20%.
  • a high-pressure impact type disperser (ULTIMAIZER HJP30006 manufactured by Sugino Machine Limited) to obtain a colorant dispersion liquid (C1) having a solid content of 20%.
  • the above materials are mixed and heated to 100°C, dispersed using the homogenizer (ULTRA-TURRAX T50 manufactured by IKA Co., Ltd.), and then subjected to a dispersion treatment with a pressure discharge type Gaulin homogenizer to obtain a mold releasing agent dispersion liquid in which mold releasing agent particles having a volume average particle diameter of 200 nm are dispersed.
  • the ion-exchange water is added to the mold releasing agent dispersion liquid to prepare a solid content of 20%, thereby obtaining a mold releasing agent dispersion liquid (W1).
  • the above materials are put into a round stainless steel flask, 0.1N nitric acid is added to adjust pH to 3.5, and then an aqueous solution of polyaluminum chloride in which 2 parts of polyaluminum chloride (30% powdery product manufactured by Oji Paper Co., Ltd.) is dissolved in 30 parts of ion-exchange water is added.
  • the mixture is dispersed at 30°C using the homogenizer (ULTRA-TURRAX T50 manufactured by IKA Co., Ltd.), the heated to 45°C in an oil bath for heating, and held until the volume average particle diameter becomes 4.9 ⁇ m.
  • NTA nitrilotriacetic acid
  • CHELEST 70 manufactured by Chelest Corporation
  • CHELEST 70 sodium hydroxide aqueous solution
  • anionic surfactant Tica Power
  • the mixture is cooled to 20°C at a rate of 20°C/min.
  • the solution is filtered, sufficiently washed with the ion-exchanged water, and dried to obtain cyan toner particles (1) having a volume average particle diameter of 5.7 ⁇ m.
  • Cyan toner particles (2) to (11) are prepared in the same manner as in the preparation of the cyan toner particles (1), except that a pH and a temperature in a fusion and coalescence step or a usage amount of the crystalline polyester resin dispersion liquid (1) is changed as shown in Table 1.
  • the above materials are mixed in a Henschel mixer (FM75L; manufactured by Nippon Coke & Engineering Co., Ltd.) at a rotation speed of 20s -1 and for a rotation time of 15 minutes to obtain a toner composition.
  • the toner composition is kneaded with a twin-screw kneading extruder (TEM-48SS: manufactured by Shibaura Machine Co., Ltd.) set at a temperature of 150°C, and a kneaded material is rolled and cooled to 30°C or less at an average cooling rate of 10°C/sec or more.
  • TEM-48SS twin-screw kneading extruder
  • the obtained kneaded material is coarsely pulverized to 1 mm or less by a hammer mill, finely pulverized by a jet mill (AFG; manufactured by Hosokawa Micron Corporation), and classified by an elbow jet classifier (EJ-LABO; manufactured by Nittetsu Mining Co., Ltd.) to obtain toner particle (12) having a volume average particle diameter of 6.5 ⁇ m.
  • the above materials are mixed in a Henschel mixer (FM75L; manufactured by Nippon Coke & Engineering Co., Ltd.) at a rotation speed of 20s -1 and for a rotation time of 15 minutes to obtain a toner composition.
  • the toner composition is kneaded with a twin-screw kneading extruder (TEM-48SS: manufactured by Shibaura Machine Co., Ltd.) set at a temperature of 150°C, and a kneaded material is rolled and cooled to 30°C or less at an average cooling rate of 10°C/sec or more.
  • TEM-48SS twin-screw kneading extruder
  • the obtained kneaded material is coarsely pulverized to 1 mm or less by a hammer mill, finely pulverized by a jet mill (AFG; manufactured by Hosokawa Micron Corporation), and classified by an elbow jet classifier (EJ-LABO; manufactured by Nittetsu Mining Co., Ltd.) to obtain toner particle (13) having a volume average particle diameter of 6.7 ⁇ m.
  • cyan toner particle (1) to (13) 100 parts of any of the cyan toner particle (1) to (13) and 1.5 parts of hydrophobic silica particles (RY50 manufactured by Nippon Aerosil Co., Ltd.) are charged into a sample mill and mixed at a rotation speed of 10,000 rpm for 30 seconds. Next, the mixture is sieved with a vibrating sieve having an opening of 45 ⁇ m to obtain cyan toners (1) to (13).
  • the dispersion liquid is used as a raw material and granulated and dried with a spray dryer to obtain granules having a volume average particle diameter of 37 ⁇ m.
  • main firing is performed using an electric furnace at a temperature of 1450°C for 4 hours, and then heating is performed in air at a temperature of 900°C for 3 hours to obtain fired particles.
  • the fired particles are crushed and classified to obtain ferrite particles (1) having a volume average particle diameter of 35 ⁇ m.
  • An arithmetic average height Ra (JIS B0601: 2001) of a roughness curve of the ferrite particles (1) is 0.6 ⁇ m.
  • silica particles are prepared as silica particles (1).
  • the silica particles in the silica particle dispersion liquid (A) have a volume average particle diameter of 4 nm and a volume particle size distribution index of 1.2 (the volume particle size distribution index is (D84v/D16v) 1/2 which is square root of a ratio of a particle diameter D84v at 84% accumulation to a particle diameter D16v at 16% accumulation from the small diameter side in the volume-based particle size distribution).
  • silica particle dispersion liquid (A) 300 parts of the silica particle dispersion liquid (A) are charged into an autoclave equipped with a stirrer, and the stirrer is rotated at a rotation speed of 100 rpm. While the stirrer is continuously rotated, liquefied carbon dioxide is injected into the autoclave from a carbon dioxide cylinder via a pump, a pressure inside the autoclave is raised by the pump while the temperature is raised by a heater, and the inside of the autoclave is brought into a supercritical state of 150°C and 15 MPa. A pressure valve is operated to circulate supercritical carbon dioxide while keeping the inside of the autoclave at 15 MPa, and methanol and water are removed from the silica particle dispersion liquid (A). When an amount of carbon dioxide supplied into the autoclave became 900 parts, supply of carbon dioxide is stopped to obtain a powder of silica particles.
  • silica particles (2) In a state in which the inside of the autoclave is maintained at 150°C and 15 MPa by the heater and the pump to maintain the supercritical state of carbon dioxide, 50 parts of hexamethyldisilazane with respect to 100 parts of silica particles is injected into the autoclave by an entrainer pump while the stirrer of the autoclave is continuously rotated, the temperature inside the autoclave is raised to 180°C, and a reaction is carried out for 20 minutes. Next, the supercritical carbon dioxide is circulated again in the autoclave, and excess hexamethyldisilazane is removed. Next, stirring is stopped, the pressure valve is opened to release the pressure in the autoclave to atmospheric pressure, and the temperature is lowered to room temperature (25°C). In this way, silica particles (2) surface-treated with the hexamethyldisilazane are obtained. The silica particles (2) have a volume average particle diameter of 4 nm.
  • silica particles (3) In the same manner as the preparation of the silica particles (2), amounts of the tetramethoxysilane and the 7.6% ammonia water dropped when the silica particle dispersion liquid (A) is prepared are increased to change the volume average particle diameter of the silica particles in the silica particle dispersion liquid to 7 nm, thereby obtaining silica particles (3) surface-treated with the hexamethyldisilazane.
  • the silica particles (3) have a volume average particle diameter of 7 nm.
  • silica particles are prepared as silica particles (5).
  • silica particles are prepared as silica particles (6).
  • silica particles are prepared as silica particles (7).
  • barium carbonate particles (volume average particle diameter: 40 nm) are prepared as inorganic particles (9).
  • barium sulfate particles (BARIFINE BF-40, volume average particle diameter: 10 nm) are prepared as inorganic particles (10).
  • barium sulfate particles (BARIFINE BF-20, volume average particle diameter: 30 nm) are prepared as inorganic particles (11).
  • barium sulfate particles (BARIFINE BF-21, volume average particle diameter: 50 nm) are prepared as inorganic particles (12).
  • barium sulfate particles (BARIFINE BF-10, volume average particle diameter: 60 nm) are prepared as inorganic particles (13).
  • the above materials and glass beads (diameter: 1 mm, the same amount as toluene) are charged into a sand mill and stirred at a rotation speed of 190 rpm for 30 minutes, to obtain a coating agent (1) having a solid content of 11%.
  • the weight average molecular weight of the resin constituting the coating agent (1) is 150,000.
  • Coating agents (2) to (7) are obtained in the same manner as in preparation of the coating agent (1), except that the silica particles (1) are changed to any of the silica particles (2) to (7).
  • Coating agents (8) to (11) are obtained in the same manner as in preparation of the coating agent (1), except that an addition amount of the silica particles (1) is changed as follows.
  • the above materials and glass beads (diameter: 1 mm, the same amount as toluene) are charged into a sand mill and stirred at a rotation speed of 1,200 rpm for 30 minutes to obtain a coating agent (12-1) having a solid content of 5%.
  • the above materials and glass beads (diameter: 1 mm, the same amount as toluene) are charged into a sand mill and stirred at a rotation speed of 1,200 rpm for 30 minutes to obtain a coating agent (12-2) having a solid content of 8%.
  • the above materials and glass beads (diameter: 1 mm, the same amount as toluene) are charged into a sand mill and stirred at a rotation speed of 190 rpm for 30 minutes, to obtain a coating agent (13) having a solid content of 11%.
  • the weight average molecular weight of the resin constituting the coating agent (13) is 85,000.
  • the above materials and glass beads (diameter: 1 mm, the same amount as toluene) are charged into a sand mill and stirred at a rotation speed of 190 rpm for 30 minutes, to obtain a coating agent (14) having a solid content of 11%.
  • the weight average molecular weight of the resin constituting the coating agent (14) is 210,000.
  • the above materials and glass beads (diameter: 1 mm, the same amount as toluene) are charged into a sand mill and stirred at a rotation speed of 190 rpm for 30 minutes, to obtain a coating agent (15) having a solid content of 11%.
  • the above materials and glass beads (diameter: 1 mm, the same amount as toluene) are charged into a sand mill and stirred at a rotation speed of 190 rpm for 30 minutes, to obtain a coating agent (16) having a solid content of 11%.
  • the above materials and glass beads (diameter: 1 mm, the same amount as toluene) are charged into a sand mill and stirred at a rotation speed of 190 rpm for 30 minutes, to obtain a coating agent (17) having a solid content of 11%.
  • the above materials and glass beads (diameter: 1 mm, the same amount as toluene) are charged into a sand mill and stirred at a rotation speed of 190 rpm for 30 minutes, to obtain a coating agent (18) having a solid content of 11%.
  • the above materials and glass beads (diameter: 1 mm, the same amount as toluene) are charged into a sand mill and stirred at a rotation speed of 190 rpm for 30 minutes, to obtain a coating agent (19) having a solid content of 11%.
  • the above materials and glass beads (diameter: 1 mm, the same amount as toluene) are charged into a sand mill and stirred at a rotation speed of 190 rpm for 30 minutes, to obtain a coating agent (20) having a solid content of 11 %.
  • the above materials and glass beads (diameter: 1 mm, the same amount as toluene) are charged into a sand mill and stirred at a rotation speed of 190 rpm for 30 minutes, to obtain a coating agent (21) having a solid content of 11%.
  • 1000 parts of the ferrite particles (1) and 125 parts of the coating agent (1) are charged into a kneader and mixed at a room temperature (25°C) for 20 minutes. Then, the mixture is heated to 70°C and reduced in pressure to be dried.
  • a dried product is cooled to the room temperature (25°C), 125 parts of the coating agent (1) is additionally added, and the mixture is mixed at the room temperature (25°C) for 20 minutes. Then, the mixture is heated to 70°C and reduced in pressure to be dried.
  • a dried product is taken out from the kneader, and coarse powder is sieved with a mesh having a mesh size of 75 ⁇ m and removed to obtain the carrier (1).
  • Carriers (2) to (7) are obtained in the same manner as in the preparation of the carrier (1), except that the mixing time after the coating agent (1) is additionally added is changed as illustrated in Table 3.
  • Carriers (8) to (13) are obtained in the same manner as in the preparation of the carrier (1), except that the coating agent (1) is changed to any one of the coating agents (2) to (7).
  • Carriers (14) to (19) are obtained in the same manner as in the preparation of the carrier (1), except that the amount of the additionally added coating agent (1) is changed as illustrated in Table 3.
  • Carriers (20) to (23) are obtained in the same manner as in the preparation of the carrier (1), except that the coating agent (1) is changed to any one of the coating agents (8) to (11).
  • 100 parts of the ferrite particles (1) and 40 parts of the coating agent (12-1) are placed in a vacuum degassing kneader, heating and decompression are conducted with stirring, and the mixture is stirred and dried in an atmosphere of 90°C/-720 mmHg for 30 minutes.
  • 10 parts of the coating agent (12-2) is applied to the taken out carrier by a spray method, dried, and then allowed to stand at 150°C for 1 hour in an electric furnace to be fired. The coarse powder is removed by sieving with a mesh having an opening of 75 ⁇ m to obtain the carrier (24).
  • Carriers (25) to (33) are obtained in the same manner as in the preparation of the carrier (1), except that the coating agent (1) is changed to any one of the coating agents (13) to (21).
  • the specific surface area measured value of the toner particles is obtained from a nitrogen adsorption amount by BET one-point method (equilibrium relative pressure: 0.3).
  • the toner particles are taken into the flow particle image analysis apparatus (FPIA-3000 manufactured by Sysmex Corporation), the toner particles are captured, subjected to the two-dimensional image processing, and the equivalent circle diameter is calculated from the projection area. A sum of the surface areas and a sum of the volumes are calculated from equivalent circle diameters of 4,500 toner particles.
  • FPIA-3000 manufactured by Sysmex Corporation
  • Density of the toner particles is measured by measuring true density in accordance with 8.2.2 of JIS K0061: 2001 using a Gulysack type specific gravity bottle.
  • toner is tablet-molded into a disk having a diameter of 8 mm and a thickness of 4 mm in an environment of 25°C ⁇ 3°C.
  • the disk-shaped sample is placed on a parallel plate of a rheometer ("ARES" manufactured by TA Instruments Inc.).
  • the sample is adhered to a parallel plate at a temperature of 130°C, cooled to a temperature of 30°C at a cooling rate of 1°C/min, held at a temperature of 30°C for 30 minutes, and then measured at the temperature of 30°C.
  • Measurement conditions include a frequency of 1 Hz, an angular frequency of 6.28 rad/sec, and a strain of 0.03 to 20% (automatic control).
  • an electron beam three-dimensional roughness analysis apparatus ERA-8900FE manufactured by Elionix Co., Ltd. is used as a device for three-dimensional analysis of the surface of the carrier.
  • the surface analysis of the carrier by ERA-8900FE is specifically performed as follows.
  • the surface of one carrier particle is magnified 5,000 times, and three-dimensional measurement is performed by taking 400 measurement points in a long side direction and 300 points in a short side direction to obtain three-dimensional image data in a region of 24 ⁇ m ⁇ 18 ⁇ m.
  • the limit wavelength of the spline filter is set to 12 ⁇ m to remove wavelengths having a period of 12 ⁇ m or more
  • the cutoff value of the Gaussian high-pass filter is set to 2.0 ⁇ m to remove wavelengths having a period of 2.0 ⁇ m or more, so as to obtain three-dimensional roughness curve data.
  • the ratio B/A is calculated for each of 100 carriers and the arithmetic average value is obtained.
  • the carrier is embedded in an epoxy resin and cut with a microtome to prepare a carrier cross section.
  • An SEM image obtained by capturing the carrier cross section with a scanning transmission electron microscope (S-4100, manufactured by Hitachi, Ltd.) is taken into an image processing analysis apparatus (Nireco, Luzex AP), and image analysis is performed.
  • 100 silica particles (primary particles) in the resin layer are randomly selected, and an equivalent circular diameter (nm) of each particle is calculated and arithmetically averaged to obtain the average particle diameter (nm) of the silica particles.
  • the SEM image is taken into the image processing analysis apparatus (Nireco, Luzex AP) to perform the image analysis.
  • the thickness ( ⁇ m) of the resin layer is measured by randomly selecting 10 points per particle of the carrier, and 100 particles of the carrier are further selected to measure thicknesses thereof, and all the thicknesses are arithmetically averaged to obtain the average thickness ( ⁇ m) of the resin layer.
  • the carrier is used as a sample and analyzed by X-ray photoelectron spectroscopy (XPS) under the following conditions, and the silicon element concentration (atomic%) is obtained from a peak intensity of each element.
  • XPS X-ray photoelectron spectroscopy
  • a modified machine of an image forming apparatus DocuPrint Color 3540 (manufactured by Fuji Xerox Co., Ltd.) is prepared, and a developer is put into a developing device.
  • a toner of the same kind as the toner used for preparing the developer is put into the toner cartridge (for example, when the developer in the developing device is a developer in which the cyan toner (1) and the carrier (1) are combined, the cyan toner (1) is put into the toner cartridge).
  • the image forming apparatus is left in an environment at a temperature of 25°C and a relative humidity of 55% for 24 hours. Under an environment of the temperature of 25°C and the relative humidity of 55%, 50,000 sheets of cyan test images having an image density of 10% are output on A3 size paper. Next, 10 cyan solid images (image density 100%) are output on the entire surface of the A3 size paper, and whether there are white spots in the solid images is visually observed and classified as follows.

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Inorganic Chemistry (AREA)
  • Developing Agents For Electrophotography (AREA)
EP24158954.8A 2021-05-20 2022-03-31 Révélateur d'image à charge électrostatique, cartouche de traitement, appareil de formation d'image et procédé de formation d'image Pending EP4411481A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2021085621A JP2022178661A (ja) 2021-05-20 2021-05-20 静電荷像現像剤、プロセスカートリッジ、画像形成装置及び画像形成方法
EP21195638 2021-09-08
EP22165828.9A EP4092483A1 (fr) 2021-05-20 2022-03-31 Révélateur d'images à charge électrostatique, cartouche de traitement, appareil de formation d'images et procédé de formation d'images

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EP22165828.9A Pending EP4092483A1 (fr) 2021-05-20 2022-03-31 Révélateur d'images à charge électrostatique, cartouche de traitement, appareil de formation d'images et procédé de formation d'images

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001188388A (ja) * 1999-10-20 2001-07-10 Ricoh Co Ltd 電子写真用現像剤
JP2008304745A (ja) 2007-06-08 2008-12-18 Konica Minolta Business Technologies Inc 静電荷像現像用現像剤
JP2011186005A (ja) 2010-03-04 2011-09-22 Fuji Xerox Co Ltd 静電荷像現像用現像剤用キャリア、静電荷像現像用現像剤、トナーカートリッジ、プロセスカートリッジ、及び画像形成装置
US20170242354A1 (en) * 2016-02-19 2017-08-24 Fuji Xerox Co., Ltd. Electrostatic charge image developing toner, electrostatic charge image developer, and toner cartridge
JP2019168533A (ja) 2018-03-22 2019-10-03 富士ゼロックス株式会社 静電荷像現像用トナー、静電荷像現像剤、トナーカートリッジ、プロセスカートリッジ、画像形成装置、及び画像形成方法

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5640684B2 (ja) * 2010-11-12 2014-12-17 富士ゼロックス株式会社 静電写真用現像剤、プロセスカートリッジ、画像形成装置及び画像形成方法

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001188388A (ja) * 1999-10-20 2001-07-10 Ricoh Co Ltd 電子写真用現像剤
JP2008304745A (ja) 2007-06-08 2008-12-18 Konica Minolta Business Technologies Inc 静電荷像現像用現像剤
JP2011186005A (ja) 2010-03-04 2011-09-22 Fuji Xerox Co Ltd 静電荷像現像用現像剤用キャリア、静電荷像現像用現像剤、トナーカートリッジ、プロセスカートリッジ、及び画像形成装置
US20170242354A1 (en) * 2016-02-19 2017-08-24 Fuji Xerox Co., Ltd. Electrostatic charge image developing toner, electrostatic charge image developer, and toner cartridge
JP2019168533A (ja) 2018-03-22 2019-10-03 富士ゼロックス株式会社 静電荷像現像用トナー、静電荷像現像剤、トナーカートリッジ、プロセスカートリッジ、画像形成装置、及び画像形成方法

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