JP2006293290A - Toner for electrostatic image development, image forming method and process cartridge for image forming apparatus - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a toner which ensures proper dispersibility of a black metal compound of high safety and fluidity. <P>SOLUTION: The toner for electrostatic image development is obtained, by suspending a polymerizable monomer composition containing at least a polymerizable monomer and a black colorant in an aqueous dispersion medium, and carrying out polymerization with a polymerization initiator, wherein a titanium-containing black iron oxide compound, having a saturation magnetization of 0.1-50 emu/g, an L<SP>*</SP>level of a color system of 9-15, and both a<SP>*</SP>and b<SP>*</SP>levels of -1.0 to +1.0 each, is contained as the black colorant. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

  The present invention relates to an electrostatic charge image developing toner for developing an electrostatic charge image formed on the surface of an image carrier in electrophotography, electrostatic recording, electrostatic printing, and the like, and a developer and an image using the toner. The present invention relates to a forming method and a process cartridge for an image forming apparatus.

  Image formation by electrophotography generally involves forming an electric latent image on a photoconductor produced using a photoconductive substance by various means, and then developing the latent image using a developer, An image formed by a developer is transferred onto paper or the like as necessary, and further fixed by heating, pressurization, solvent vapor, or the like. In the case of full-color image formation, the toner is obtained using toners of four colors of black, yellow, magenta, and cyan.

In black toner, carbon black is generally used as a colorant. Recently, attempts have been made to use black metal compound fine powder as a colorant replacing carbon black (for example, see Patent Documents 1 to 10). .) For example, in Patent Document 1, a mixture of Fe ₂ TiO ₅ and Fe ₂ O ₃ —FeTiO ₃ solid solution having an average particle size of 0.1 to 0.5 μm is contained, and in Patent Documents 2 to 4, a magnetic material containing 25 to 30% FeO. In patent documents 5 and 6, iron oxide is magnetite having a remanent magnetization of 6 emu / g or less, in patent document 7, iron oxide particles composed of Ti inside, Ti and Fe on the surface, and in patent document 8, saturation magnetization 0.5. A rutile type TiO ₂ mixed phase crystal coated with Fe ₂ TiO ₄ is a metal having a saturation magnetization of 30 emu / g or less and a dielectric loss factor of 50 or less. In Patent Document 10, a metal compound having a saturation magnetization of 40 emu / g or less and a content of 20 parts by weight or less has been devised.
Japanese Patent No. 2736680 Japanese Patent No. 3101782 Japanese Patent No. 3108823 Japanese Patent No. 3174960 Japanese Patent No. 3224774 Japanese Patent No. 3261888 JP 2000-319021 A JP 2002-129063 A JP 2002-189313 A JP 2002-196528 A

  In the above prior art, by using a black metal compound that has high safety and good fluidity as a colorant, the thermal conductivity is higher than that of carbon black, and it can be fixed at a lower temperature. Since the specific gravity is high, advantages such as easy mixing with the carrier in the developer were obtained. However, in the toner prepared by the pulverization method, the dispersibility of the metal compound was insufficient and excellent. There was a problem that the performance could not be fully demonstrated.

  As a result of intensive studies, the present inventors have studied the polymerizable monomer composition containing at least a polymerizable monomer and a colorant in an aqueous dispersion medium containing a dispersion stabilizer. It has been found that the use of a black iron oxide compound containing titanium is extremely effective as a colorant in a polymerized toner obtained by suspending the product and polymerizing with a polymerization initiator.

  The present invention has been made on the basis of such knowledge, and an electrostatic image developing toner capable of obtaining a high-definition image with good dispersibility of the colorant in the toner, little background stain, and the like. The purpose is to provide.

  Another object of the present invention is to provide an image forming method and a process cartridge for an image forming apparatus that can obtain a high-definition image by using the toner for developing an electrostatic charge image.

That is, the invention of claim 1 suspends a polymerizable monomer composition containing at least a polymerizable monomer and a black colorant in an aqueous dispersion medium and performs polymerization using a polymerization initiator. In the resulting electrostatic image developing toner, the black colorant has a saturation magnetization of 0.1 to 50 emu / g, a color system L ^* value of 9 to 15, and a ^* and b ^* of -1. It is characterized by containing 15 to 35% by weight of a black iron oxide compound containing titanium in the range of 0 to +1.0.

  According to a second aspect of the present invention, in the electrostatic image developing toner of the first aspect, the black iron oxide compound contains a titanium component in an amount of 10 to 45% by weight with respect to Fe atoms in terms of Ti atoms.

According to a third aspect of the present invention, in the electrostatic charge image developing toner according to the first or second aspect, the specific surface area of the black iron oxide compound is 1.3 to 80 m ² / g.
The

The invention according to claim 4 is the electrostatic image developing toner according to any one of claims 1 to 3, wherein the true specific gravity of the black iron oxide compound is 4.0 to 5.0 g / cm ^3. To do.

  According to a fifth aspect of the present invention, in the electrostatic image developing toner according to any one of the first to fourth aspects, the average primary particle size of the black iron oxide compound is 0.05 to 2.0 μm. .

  According to a sixth aspect of the present invention, in the electrostatic image developing toner according to any one of the first to fifth aspects, the volume average particle size of the toner particles is 3 to 8 μm, and the volume average particle size / number average particle size is The expressed particle size ratio is 1.0 to 1.5.

  According to a seventh aspect of the present invention, in the electrostatic image developing toner according to any one of the first to sixth aspects, the average circularity of the toner particles is 0.96 to 1.00.

  According to an eighth aspect of the present invention, in the electrostatic image developing toner according to any one of the first to seventh aspects, a wax is contained as a release agent.

  According to a ninth aspect of the present invention, in the electrostatic image developing toner according to any one of the first to eighth aspects, a charge control agent is contained.

  The invention according to claim 10 is characterized in that the one-component developer comprises the electrostatic image developing toner according to any one of claims 1 to 9.

  An eleventh aspect of the invention is characterized in that the two-component developer comprises the electrostatic image developing toner according to any one of the first to ninth aspects and a carrier.

  A twelfth aspect of the present invention is a toner container filled with the electrostatic image developing toner according to any one of the first to ninth aspects.

  According to a thirteenth aspect of the present invention, in the image forming method, the electrostatic image developing toner according to any one of the first to ninth aspects is used.

  The invention of claim 14 is a process cartridge for an image forming apparatus comprising at least an image carrier and developing means, wherein the developer according to claim 10 or 11 is stored in the developing means. .

  According to the present invention, the dispersibility of the black iron oxide compound in the toner is good, and it can be finely dispersed uniformly as compared with the pulverized toner. Therefore, high image density and low temperature fixing are possible, and charging is possible. An electrostatic charge image developing toner free from defects, background contamination and toner scattering can be obtained.

Hereinafter, the best mode for carrying out the present invention will be described.
<Black iron oxide compound>
By using a black iron oxide compound as a black colorant in the toner for developing an electrostatic image, the content of carbon black having a high conductivity imparting effect can be reduced or zero.
As a result, non-image area stains and toner scattering occur due to a decrease in charge resistance and a decrease in charge retention capacity, resulting in a decrease in chargeability and an increase in the amount of reversely charged toner and weakly charged toner. Problems are less likely to occur.

  The saturation magnetization value of the black iron oxide compound is preferably 50.0 emu / g or less. By setting the saturation magnetization value to 50 emu / g or less, the saturation magnetization of the toner can be made extremely small, and when used as a non-magnetic toner, a developer carrier of a one-component developer or a two-component developer This is because there is no problem of deterioration in developability due to an increase in magnetic binding force on the carrier.

  The magnetic properties can be measured using a magnetism measuring apparatus BHU-60 manufactured by Riken Denshi Co., Ltd. Specifically, a magnetic field is applied to a toner filled in a cell having an inner diameter of 7 mmΦ and a height of 10 mm with a magnetic field of 10 kOe. Saturation magnetization, residual magnetization, and coercive force were obtained from the hysteresis curve when swept up to.

As an index representing the blackness of the black iron oxide compound, CIE 1976 (L ^* , a ^* , b ^* ) uniform perceptual color space, the so-called L ^* a ^* b ^* color system lightness L ^* value is 9 to 20, a ^* and It is preferable that all b ^* are in the range of -2.0 to 3.0.
In particular, it is more preferable that the L ^* value is 15 or less and both a ^* and b ^* are in the range of -1.0 to 1.0 because a sufficient coloring degree is easily obtained.

The L ^* value, a ^* value, and b ^* value were measured using an X-Rite 938 after preparing a sample piece for measurement. As a specific sample piece for measurement, 0.5 g of black iron oxide powder and 1.0 cc of castor oil were kneaded with a Hoover-type Mahler to form a paste, and 4.5 g of clear lacquer was added to the paste and kneaded to prepare a paint. Then, it produced by apply | coating on a cast coat paper using a 6 mil applicator.

In the present invention, since the black iron oxide compound containing titanium does not use PRTR (environmental pollutant discharge transfer registration) target substance among black metal materials, it has also been noted that it is preferable considering the influence on the environment.
As the structure of this compound, a polycrystalline particle powder containing a Fe ₂ O ₃ —FeTiO ₃ solid solution is preferable because it is black and non-magnetic. The amount of the titanium compound in this compound is preferably in the range of 10 to 45 weights of the titanium component with respect to Fe atoms in terms of Ti atoms. When the amount is less than 10% by weight, the magnetization value of the obtained black pigment particle powder becomes large. If it exceeds 45% by weight, a non-magnetic black pigment particle powder is obtained, but the L ^* value increases because the amount of TiO ₂ produced increases.

The ratio with respect to Fe atoms in terms of Ti atoms can be obtained from the ratio of the main peak obtained per mol using a wavelength dispersive X-ray fluorescence analyzer.
The wavelength dispersive X-ray fluorescence analysis method uses RIX3000 manufactured by Rigaku Corporation. The sample is pressure molded into an aluminum ring of 32 mmΦ under the conditions of spectroscopic crystal LiF, output 50 kV, current 50 mA, target Rh, measurement range 30 mmΦ. And measure.

The specific surface area of the black iron oxide compound is preferably in the range of 1.3 to 80 m ² / g.
Further, from the viewpoint of dispersibility in the toner, the range of 1.5 to 30 m ² / g is more preferable. When it exceeds 80 m ² / g, depending on the content, the metal material acts as a filler and hardly contributes to low-temperature fixability. When it is less than 1.3 m ² / g, the colorability becomes insufficient.

The specific surface area Sb (m ² / g) per unit weight measured by the BET method and the specific surface area per unit weight calculated from the weight average particle diameter when the toner is assumed to be a true sphere is St (m ² / g). The ratio Sb / St.
The BET specific surface area is measured by a multi-point method of nitrogen adsorption method, specifically, a high-speed specific surface area / pore distribution measuring device NOVA1200 multi-point method manufactured by Yuasa Ionics Co., Ltd.
Conditionally adsorbed gas: nitrogen gas (99.995 or higher)
Refrigerant: Liquid nitrogen cell: 9mm pellet short (large)
Pretreatment conditions: 30 ° C for 12 hours (evacuation)
Measurement points: Measured at 3 points of relative pressure (P / PO) = 0.1 to 0.3.

The true specific gravity of the black iron oxide compound is preferably 4.0 to 5.0 g / cm ³ .
By using a metal material in this range, the true specific gravity of the toner can be appropriately increased, the specific gravity difference can be reduced in the stirring of the toner and the carrier, and the stirring efficiency of the toner and the carrier is excellent.

The true specific gravity of the black iron oxide compound can be determined with an air-comparing hydrometer 930 type (Beckman).
In the measurement, a sample of about 5 g is carefully evaluated to 4 decimal places g, the true volume is obtained under the condition of 2 atm using the measuring device, and the true specific gravity is obtained by dividing the sample weight by the true volume.

The content of the black iron oxide compound is preferably 15 to 35% by weight.
When the content is less than 15% by weight, the degree of coloring of the toner is insufficient. On the other hand, when the content exceeds 35% by weight, the low-temperature fixability is deteriorated due to the shortage of the resin component, and the toner volume specific resistance due to aggregation of the black metal material. And toner charging failure, background stains, and toner scattering due to the reduction of the toner density are noticeable.

  The average primary particle diameter of the black iron oxide compound is preferably in the range of 0.05 to 2.0 μm, and particularly preferably in the range of 0.1 to 0.5 μm from the viewpoint of dispersibility in the toner.

The average primary particle diameter of the black iron oxide compound is measured by the following method.
Black iron oxide compound is collected on carbon tape, coated with Pt-Pd, and then an SEM image magnified 15000 times at an acceleration voltage of 10 kv using an electron microscope such as a Hitachi scanning electron microscope H-9000. To do.
This image is taken into a Luzex image analyzer manufactured by Nireco Corporation, and the average primary particle size is calculated from 50 or more photographs of black iron oxide compounds.

The black iron oxide compound contained in the toner for developing an electrostatic charge image of the present invention is, for example, a magnetite particle powder having a particle surface coated with a titanium compound, a mixed powder of magnetite particle powder and a titanium compound, or a particle surface having a titanium compound. The hematite particle powder coated with the above is reduced, and each of the obtained reduced powders is heated and fired at a temperature of 700 ° C. or higher in a non-oxidizing atmosphere and then pulverized.
When magnetite particle powder whose particle surface is coated with a titanium compound is used as a raw material, it is a preferable method from the viewpoint of easily obtaining particles having a small magnetization value and non-magnetism.

  The magnetite particle powder and hematite particle powder may be particles of any form such as granular, spherical, and needle-like, and particles having a size of about 0.03 to 1.5 μm can be used. There is a correlation between the size of the raw material particles and the size of the product particles. When small raw material particles are used, small product particles tend to be obtained, and when large raw material particles are used, large product particles tend to be obtained. It is in.

As the titanium compound, any of hydrated oxide, hydroxide and oxide of titanium can be used. When mixing with magnetite particle powder, it is preferable to use a water-soluble titanium compound. The amount of the titanium compound is preferably in the range of 10 to 45 wt. When the amount is less than 10% by weight, the magnetization value of the obtained black pigment particle powder becomes large. If it exceeds 45% by weight, a non-magnetic black pigment particle powder is obtained, but the L ^* value increases because the amount of TiO ₂ produced increases.

As the non-oxidizing atmosphere, N ₂ gas or the like can be used. When the atmosphere is oxidizing, the target black iron oxide compound cannot be obtained. The heating and firing temperature needs to be 700 ° C. or higher. When the temperature is lower than 700 ° C., the solid phase reaction between iron oxide and titanium compound does not occur sufficiently, and the desired black pigment particle powder cannot be obtained. The pulverization can be performed using a pulverizer such as a commonly used ball mill, attritor, or vibration mill.

  In the above method, if necessary, the raw material particles may be coated with a known sintering inhibitor before heating and firing. In this case, it is possible to prevent sintering between the particles and the particles during heating and firing, and it is possible to obtain black pigment particle powder having excellent dispersibility.

  As a sintering inhibitor that does not impair various properties of the black pigment particle powder that is the object of the present invention, a compound comprising one or more elements selected from Al, Ti, Si, Zr and P is used. Can do. The amount of the sintering inhibitor is 0.1 to 15.0 atomic% with respect to Fe and Ti. In order to obtain a sufficient sintering prevention effect, it is preferably 0.1 atomic% or more, and when it exceeds 15.0 atomic%, magnetite is mixed in the resulting black pigment particle powder, and non-magnetic It becomes difficult to obtain a black iron oxide compound.

In order to further increase the blackness, it is preferable to fix the black dyed pigment and the blue dyed pigment to the surface of the black pigment particles using a Mechanomyl (Okada Seiko Co., Ltd.) or a MechanoFusion System (Hosokawa Micron Co., Ltd.).
Black dyes and pigments include iron black, aniline black, graphite, fullerene, and blue dyes and pigments include cobalt blue, alkali blue, Victoria blue lake, phthalocyanine blue, metal-free phthalocyanine blue, phthalocyanine blue partially chlorinated, and first sky blue. , Indanthrene Blue BC and the like, but are not limited thereto.

<Polymerizable monomer>
As the polymerizable monomer used in the present invention, a monomer having a vinyl group is preferable. Specific examples of the polymerizable monomer include, for example, aromatic vinyl monomers such as styrene, α-methylstyrene, p-methylstyrene, p-chlorostyrene, and vinyltoluene; non-acrylic monomers such as acrylonitrile and methacrylonitrile. Saturated nitriles; unsaturated (meth) acrylic acids such as methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, lauryl (meth) acrylate, stearyl (meth) acrylate Esters; acrylic acids such as acrylic acid and methacrylic acid; ethylenically unsaturated monoolefins such as ethylene, propylene, butylene, and isobutylene; vinyl halides such as vinyl chloride, vinylidene chloride, vinyl bromide, and vinyl fluoride; Such as vinyl acetate and vinyl propionate Nyl esters; vinyl ethers such as vinyl methyl ether and vinyl ethyl ether; vinyl ketones such as vinyl methyl ketone and methyl isopropenyl ketone; nitrogen-containing vinyl compounds such as 2-vinyl pyridine, 4-vinyl pyridine and N-vinyl pyrrolidone; Examples thereof include conjugated diolefins such as butadiene and isoprene. These polymerizable monomers can be used alone or in combination of two or more. In addition, it is not necessary to make a polymerization inhibitor coexist in a monomer.

  Along with these vinyl monomers, crosslinkable monomers, for example, aromatic divinyl compounds such as divinylbenzene, divinylnaphthalene, and derivatives thereof; ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacrylate, triethylene glycol Di- or tri-ethylenically unsaturated carboxylic esters such as methylolpropane triacrylate, 1,3-butanediol dimethacrylate; divinyl compounds such as N, N-divinyl amylin, divinyl ether, divinyl sulfide, divinyl sulfone, and 3 One or more compounds having one or more vinyl groups can be used in combination. These crosslinkable monomers can be added before the start of polymerization or in the middle of the polymerization, and are generally 0 to 20% by weight, preferably 0.1 to 5 parts by weight in the total monomers. Used in

<Molecular weight regulator>
Examples of the molecular weight modifier include mercaptans such as t-dodecyl mercaptan, n-dodecyl mercaptan, and n-octyl mercaptan; halogenated hydrocarbons such as carbon tetrachloride and carbon tetrabromide. These molecular weight modifiers can be added to the reaction system before the start of polymerization or during the polymerization. The molecular weight regulator is used in an amount of 0.01 to 10 parts by weight, preferably 0.1 to 5 parts by weight, based on 100 parts by weight of the polymerizable monomer.

<Charge control agent>
As the charge control agent, various positively chargeable or negatively chargeable charge control agents can be used. For example, a metal complex of an organic compound having a carboxyl group or a nitrogen-containing group, a metal-containing dye, nigrosine and the like can be mentioned. More specifically, Spiron Black TRH (made by Hodogaya Chemical Co., Ltd.), T-77 (made by Hodogaya Chemical Co., Ltd.), Bontron S-34 (made by Orient Chemical Co., Ltd.), Bontron E-84 (made by Orient Chemical Co., Ltd.), Bontron N -01 (manufactured by Orient Chemical Co., Ltd.), Copy Blue-PR (manufactured by Hoechst), etc. and / or quaternary ammonium (salt) group-containing copolymers, sulfonic acid (salt) group-containing copolymers, etc. A charge control resin can be used. The charge control agent is preferably used in an amount of 0.01 to 10 parts by weight, more preferably 0.03 to 8 parts by weight, based on 100 parts by weight of the polymerizable monomer.

<Polymerization initiator>
Examples of the polymerization initiator used in the present invention include persulfates such as potassium persulfate and ammonium persulfate; 4,4′-azobis (4-cyanovaleric acid), 2,2′-azobis (2-amidinopropane) dihydrochloride Salt, 2,2′-azobis-2-methyl-N-1,1′-bis (hydroxymethyl) -2-hydroxyethylpropioamide, 2,2′-azobis (2,4-dimethylvaleronitrile), Azo compounds such as 2,2′-azobisisobutyronitrile and 1,1′-azobis (1-cyclohexanecarbonitrile); methyl ethyl peroxide, di-t-butyl peroxide, acetyl peroxide, dicumylper Oxide, lauroyl peroxide, benzoyl peroxide, t-butylperoxy-2-ethylhexanoate, t-butylperoxyneodecanoate, Examples thereof include peroxides such as t-butyl peroxypivalate, di-isopropyl peroxydicarbonate, and di-t-butyl peroxyisophthalate. Moreover, the redox initiator which combined these polymerization initiators and reducing agents can be mentioned. Among these, it is preferable to select an oil-soluble initiator that is soluble in the polymerizable monomer to be used, and a water-soluble initiator can be used in combination with this if necessary. The polymerization initiator is used in an amount of 0.1 to 20 parts by weight, preferably 0.3 to 15 parts by weight, more preferably 0.5 to 10 parts by weight, based on 100 parts by weight of the polymerizable monomer. is there.

<Release agent>
Examples of the release agent used as necessary in the present invention include, for example, low molecular weight polyolefin waxes such as low molecular weight polyethylene, low molecular weight polypropylene, and low molecular weight polybutylene, molecular terminal oxidized low molecular weight polypropylene, and molecular terminals based on epoxy groups. End-modified polyolefin waxes such as substituted low molecular weight end-modified polypropylene and block polymers of these and low molecular weight polyethylene, molecular end oxidized low molecular weight polyethylene, low molecular weight polyethylene having molecular ends substituted with epoxy groups, and block polymers of these and low molecular weight polypropylene Plant-based natural waxes such as candelilla, carnauba, rice, tree wax, jojoba; petroleum waxes such as paraffin, microcrystalline, petrolactam and their modified waxes; montan, ceresin Synthetic waxes such as Fischer-Tropsch wax; mineral waxes ozokerite such pentaerythritol myristate, one such multifunctional ester compounds such as pentaerythritol tetra palmitate or two or more can be exemplified.

  Of these, synthetic wax (especially Fischer-Tropsch wax), synthetic polyolefin, low molecular weight polypropylene wax, microcrystalline wax and the like are preferable. Among them, in the DSC curve measured by a differential scanning calorimeter, the endothermic peak temperature at the time of temperature rise is in the range of 30 to 200 ° C., preferably 50 to 180 ° C., and 60 to 160 ° C. This is particularly preferable in terms of the peelability balance. The endothermic peak temperature is a value measured by ASTM D3418-82. The mold release agent may be used in an amount of 0.1 to 20 parts by weight, more preferably 1 to 10 parts by weight with respect to 100 parts by weight of the polymerizable monomer.

<Dispersant>
Examples of the dispersant used in the present invention include sulfates such as barium sulfate and calcium sulfate; carbonates such as barium carbonate, calcium carbonate and magnesium carbonate; phosphates such as calcium phosphate; metal oxides such as aluminum oxide and titanium oxide. Metal hydroxides such as aluminum hydroxide, magnesium hydroxide, and ferric hydroxide; water-soluble polymers such as polyvinyl alcohol, methylcellulose, gelatin; anionic surfactants, nonionic surfactants And amphoteric surfactants. Of these, a dispersant containing a metal compound, particularly a colloid of a poorly water-soluble metal hydroxide, is preferable because the particle size distribution of the polymer particles can be narrowed and the sharpness of the image is improved. . In particular, when a crosslinkable monomer is not copolymerized, a dispersant containing a hardly water-soluble metal hydroxide colloid improves the dispersion stability of the polymer particles during vacuum stripping, as well as toner fixability and storage. It is suitable for improving the property.

  The dispersant containing the colloid of the hardly water-soluble metal hydroxide is not limited by its production method, but the hardly water-soluble metal water obtained by adjusting the pH of the aqueous solution of the water-soluble polyvalent metal compound to 7 or more. It is preferable to use a colloid of an oxide, particularly a colloid of a poorly water-soluble metal hydroxide produced by a reaction in a water phase of a water-soluble polyvalent metal compound and an alkali metal hydroxide.

  The colloid of the poorly water-soluble metal compound used in the present invention has a number particle size distribution D50 (50% cumulative value of the number particle size distribution) of 0.5 μm or less and a D90 (90% cumulative value of the number particle size distribution) of 1 μm. The following is preferable. When the particle size of the colloid is increased, the stability of polymerization is lost and the storage stability of the toner is lowered.

  The dispersant is usually used in a proportion of 0.1 to 20 parts by weight, preferably 0.3 to 10 parts by weight, with respect to 100 parts by weight of the polymerizable monomer. When this ratio is small, it is difficult to obtain sufficient polymerization stability and dispersion stability during vacuum stripping, and aggregates are likely to be formed. Conversely, if this ratio is large, the toner particle size becomes too fine, which is not preferable.

<Suspension polymerization>
In the present invention, a known method may be employed for suspension polymerization. For example, a mixture containing an additive such as a polymerizable monomer, a colorant, a molecular weight adjusting agent, a charge control agent, and a release agent is put into an aqueous dispersion medium and stirred to granulate droplet particles. Depending on the method, polymerization may be carried out by stirring and raising the temperature in the presence of a polymerization initiator. The aqueous dispersion medium may contain a dispersion stabilizer. The polymer particle dispersion thus obtained is the polymer particle dispersion referred to in the present invention. When the toner is manufactured, a dehydration and drying process is then performed to remove the dispersion medium.

<External additive>
As the external additive for assisting the fluidity, developability and chargeability of the colored particles obtained in the present invention, inorganic fine particles can be preferably used. The primary particle diameter of the inorganic fine particles is preferably 5 nm to 2 μm, and particularly preferably 5 nm to 500 nm. Moreover, it is preferable that the specific surface area by BET method is 20-500 m < ² > / g. The proportion of the inorganic fine particles used is preferably 0.01 to 5.0% by weight of the toner, and particularly preferably 0.01 to 2.0% by weight.

  Specific examples of the inorganic fine particles include, for example, silica, alumina, titanium oxide, barium titanate, magnesium titanate, calcium titanate, strontium titanate, zinc oxide, tin oxide, quartz sand, clay, mica, wollastonite, diatomaceous earth. Examples include soil, chromium oxide, cerium oxide, bengara, antimony trioxide, magnesium oxide, zirconium oxide, barium sulfate, barium carbonate, calcium carbonate, silicon carbide, and silicon nitride.

  In addition, polymer fine particles such as polystyrene obtained by soap-free emulsion polymerization, suspension polymerization and dispersion polymerization, methacrylic acid ester and acrylic acid ester copolymer, polycondensation system such as silicone, benzoguanamine and nylon, thermosetting resin And polymer particles.

  Such a fluidizing agent can be surface-treated to increase hydrophobicity and prevent deterioration of flow characteristics and charging characteristics even under high humidity. For example, silane coupling agents, silylating agents, silane coupling agents having an alkyl fluoride group, organic titanate coupling agents, aluminum coupling agents, silicone oils, modified silicone oils and the like are preferable surface treatment agents. It is done.

  Examples of the cleaning property improver for removing the developer after transfer remaining on the photosensitive member or the primary transfer medium include fatty acid metal salts such as zinc stearate, calcium stearate and stearic acid, such as polymethyl methacrylate fine particles, polystyrene. Examples thereof include polymer fine particles produced by soap-free emulsion polymerization of fine particles and the like. The polymer fine particles preferably have a relatively narrow particle size distribution and a volume average particle size of 0.01 to 1 nm.

<Circularity and circularity distribution>
It is important that the toner in the present invention has a specific shape and shape distribution, the average circularity is less than 0.950, and a toner having an irregular shape that is too far from a spherical shape is satisfactory. High-quality images with no transferability or dust are not obtained.
As a method for measuring the shape, an optical detection band method is suitable in which a suspension containing particles is passed through an imaging unit detection band on a flat plate, and a particle image is optically detected and analyzed by a CCD camera. is there. A toner having an average circularity of 1.000 to 0.960, which is a value obtained by dividing the perimeter of an equivalent circle having the same projected area obtained by this method by the perimeter of the actual particle, has high reproducibility with an appropriate density. It was confirmed to be effective for forming a fine image. More preferably, particles having an average circularity of 0.980 to 0.960 and a circularity of less than 0.94 are 15% or less.

The average circularity is measured by a flow type particle image analyzer FPIA-2100 (manufactured by Toa Medical Electronics Co., Ltd.).
In the measurement method, 0.1 to 0.5 ml of a surfactant, preferably alkylbenzene sulfonate, is added as a dispersant to 100 to 150 ml of water from which impure solids have been removed in advance. Add about 1-0.5g.
The suspension in which the sample is dispersed is obtained by performing dispersion treatment with an ultrasonic disperser for about 1 to 3 minutes, and measuring the shape and distribution of the toner with the above apparatus at a dispersion concentration of 3000 to 10,000 / μl. .

<Ratio of volume average particle diameter / number average particle diameter>
The volume average particle diameter of the toner in the present invention is 3 to 8 μm, and the ratio to the number average particle diameter is preferably 1.0 to 1.5, and more preferably 1.0 to 1.4. desirable.
When such a dry toner is applied to a full-color copying machine or the like, it is possible to form an image with excellent glossiness. Further, when a two-component developer combined with a predetermined carrier is used, the toner balance over a long period of time is achieved. Even if the toner particle diameter varies in the developer, good and stable developability can be obtained even with long-term stirring in the developing device.
Further, when used as a one-component developer, even if the balance of the toner is performed, the fluctuation of the toner particle diameter is reduced, the toner is filmed on the developing roller, and the toner is thinned. The toner can be effectively prevented from fusing to a member such as a blade, and good and stable developability and images can be obtained even when the developing device is used (stirred) for a long time.

Note that the average particle size and particle size distribution of the toner can be measured by a car Coulter counter method.
Examples of the measuring device for the particle size distribution of the toner particles include Coulter Counter TA-II and Coulter Multisizer II (both manufactured by Coulter).
Specifically, a method of connecting and measuring an interface (Nikka Giken) that outputs a number distribution and volume distribution and a PC9801 personal computer (manufactured by NEC) using a Coulter counter TA-II type will be described.
First, 0.1 to 5 ml of a surfactant (preferably alkylbenzene sulfonate) is added as a dispersant to 100 to 150 ml of the electrolytic aqueous solution. Here, the electrolytic solution is a solution prepared by preparing a 1% NaCl aqueous solution using primary sodium chloride. For example, ISOTON-II (manufactured by Coulter) can be used.
Here, 2 to 20 mg of a measurement sample is further added. The electrolytic solution in which the sample is suspended is subjected to a dispersion treatment with an ultrasonic disperser for about 1 to 3 minutes, and the measurement device is used to measure the volume and number of toner particles or toner using a 100 μm aperture as an aperture. Volume distribution and number distribution are calculated.
As channels, 2.00 to less than 2.52 μm; 2.52 to less than 3.17 μm; 3.17 to less than 4.00 μm; 4.00 to less than 5.04 μm; 5.04 to less than 6.35 μm; 6 .35 to less than 8.00 μm; 8.00 to less than 10.08 μm; 10.08 to less than 12.70 μm; 12.70 to less than 16.00 μm; 16.00 to less than 20.20 μm; Uses 13 channels of less than 40 μm; 25.40 to less than 32.00 μm; 32.00 to less than 40.30 μm, and targets particles having a particle size of 2.00 μm to less than 40.30 μm.
The volume-based volume average particle diameter (Dv) obtained from the volume distribution according to the present invention and the number average particle diameter (Dn) obtained from the number distribution and the ratio Dv / Dn were obtained.

  In general, it is said that the smaller the particle size of the toner, the more advantageous it is to obtain a high-resolution and high-quality image, but it is disadvantageous for transferability and cleaning properties. is there. Further, when the volume average particle diameter is smaller than the range of the present invention, in the case of a two-component developer, the toner is fused to the surface of the carrier during long-term agitation in the developing device, and the charging ability of the carrier is lowered or the one-component development is performed. When used as an agent, toner filming on the developing roller and toner fusion to a member such as a blade for thinning the toner are likely to occur.

  On the contrary, when the volume particle diameter of the toner is larger than the range of the present invention, it becomes difficult to obtain a high-resolution and high-quality image, and when the balance of the toner in the developer is performed, the toner In many cases, the fluctuation of the particle size of the particles becomes large. The same applies when the volume average particle diameter / number average particle diameter is larger than 1.5.

<Two-component carrier>
When the toner of the present invention is used for a two-component developer, it may be used by mixing with a magnetic carrier, and the content ratio of the carrier and the toner in the developer is 1 to 10 weights of toner with respect to 100 parts by weight of the carrier. Part is preferred. As the magnetic carrier, conventionally known ones such as iron powder, ferrite powder, magnetite powder, magnetic resin carrier having a particle diameter of about 20 to 200 μm can be used.

  Examples of the coating material include amino resins such as urea-formaldehyde resin, melamine resin, benzoguanamine resin, urea resin, polyamide resin, and epoxy resin. Polyvinylidene and polyvinylidene resins such as acrylic resins, polymethyl methacrylate resins, polyacrylonitrile resins, polyvinyl acetate resins, polyvinyl alcohol resins, polyvinyl butyral resins, polystyrene resins and styrene acrylic copolymer resins, Halogenated olefin resins such as vinyl chloride, polyester resins such as polyethylene terephthalate resin and polybutylene terephthalate resin, polycarbonate resins, polyethylene resins, polyvinyl fluoride resins, polyvinylidene fluoride resins, polytrifluoroethylene resins, polyhexa Fluoropropylene resin, copolymer of vinylidene fluoride and acrylic monomer, copolymer of vinylidene fluoride and vinyl fluoride, tetrafluoroethylene and vinylidene fluoride Dorukatan monomer and fluoroterpolymers such as terpolymers of, and silicone resins.

  Moreover, you may contain electrically conductive powder etc. in coating resin as needed. As the conductive powder, metal powder, carbon black, titanium oxide, tin oxide, zinc oxide or the like can be used. These conductive powders preferably have an average particle diameter of 1 μm or less. When the average particle diameter is larger than 1 μm, it becomes difficult to control electric resistance.

  The toner of the present invention can also be used as a one-component magnetic toner that does not use a carrier, or a non-magnetic toner (one-component developer). The toner of the present invention can be filled in a predetermined container to form a toner container as a whole, and can be detachable from a predetermined image forming apparatus.

  Further, the one-component developer and the two-component developer of the present invention can be stored in the developing means of the process cartridge. The process cartridge referred to in the present invention is one apparatus component including an image carrier (typically, an electrophotosensitive member) and at least a developing unit.

  Hereinafter, the toner for developing an electrostatic charge image and the image forming method using the same according to the present invention will be described in detail with specific examples, but the present invention is not limited thereto. In addition, a part shows a weight part.

[Example 1]
80 parts of styrene, 20 parts of methyl methacrylate, 2 parts of release agent (synthetic polyolefin), 27 parts of metal material (metal material 1 in Table 1), 1 part of charge control agent (T-77 manufactured by Hodogaya Chemical Co., Ltd.), and polymerization start As the agent, 5 parts of lauroyl peroxide was dispersed with a ball mill at room temperature to obtain a uniform mixed solution. Next, the above mixed solution is added to 400 parts of pure water in which 4 parts of barium sulfate is finely dispersed, and then high shear stirring is performed by a rotor stutter type homomixer, and the above mixed solution is finely dispersed in water. I let you. Next, this aqueous dispersion was put into a reactor equipped with a stirring blade and polymerized at 80 ° C. for 5 hours with stirring. The polymer dispersion thus obtained was sufficiently washed with acid and water, and then separated and dried to obtain (Toner 1).

[Example 2]
(Toner 2) was obtained by the same method as in Example 1 except that the metal material 1 in Example 1 was changed to the metal material 2 in Table 1.

Example 3
(Toner 3) was obtained in the same manner as in Example 1 except that the metal material 1 in Example 1 was changed to the metal material 3 in Table 1.

Example 4
(Toner 4) was obtained by the same method as in Example 1 except that the metal material 1 in Example 1 was changed to the metal material 4 in Table 1.

[Comparative Example 1]
(Toner 5) was obtained by the same method as in Example 1 except that the metal material 1 in Example 1 was changed to the metal material 5 in Table 1.

[Comparative Example 2]
(Toner 6) was obtained in the same manner as in Example 1 except that the amount of the metal material 1 in Example 1 was changed to 10 parts.

[Comparative Example 3]
(Toner 7) was obtained in the same manner as in Example 1 except that the amount of the metal material 1 in Example 1 was changed to 90 parts.

[Comparative Example 4]
(Toner 8) was obtained in the same manner as in Example 1 except that the metal material 1 in Example 1 was changed to carbon black.

[Comparative Example 5]
(Toner 9) was obtained in the same manner as in Example 1 except that the metal material 1 in Example 1 was changed to the metal material 2 in Table 1 and the amount was changed to 14 parts.

[Comparative Example 6]
(Toner 10) was obtained by the same method as in Example 1 except that the metal material 1 in Example 1 was changed to the metal material 2 in Table 1 and the amount was changed to 74 parts.

  The physical properties and the like of the metal materials 1 to 5 described above are shown in Table 1 below, and the physical properties and the like of the obtained toner 1 to toner 10 are shown in Table 2 below.

<Preparation of two-component developer>
To 100 parts of the obtained toner, 0.7 part of hydrophobic silica and 0.3 part of hydrophobic titanium oxide were mixed with a Henschel mixer. A developer comprising 5% by weight of the toner subjected to the external additive treatment and 95% by weight of a copper-zinc ferrite carrier having an average particle diameter of 40 μm coated with a silicone resin is prepared and evaluated according to the following evaluation items. went.
The evaluation results are shown in Table 3 below.

Next, image formation is performed using the toner, and the following evaluation is performed.
<Evaluation items>
(1) Low-temperature fixability Using a Ricoh copier, imagio Neo450, a solid image having an adhesion amount of 1.0 ± 0.1 mg / cm ² was prepared on a copy paper (TYPE6000 <70W>, manufactured by Ricoh). Fixing conditions Fixing machine linear speed: 180 ± 2 mm / sec. Fixing nip width: 10 ± 1 mm
Then, the temperature of the fixing roller was changed, and the cold offset temperature (fixing lower limit temperature) was measured. The low temperature fixability was evaluated according to the measurement temperature in the following five steps.
5: Less than 130 ° C, 4: 130 ° C or more and less than 140 ° C, 3: 140 ° C or more and less than 150 ° C, 2: 150 ° C or more and less than 160 ° C, 1: 160 ° C or more

(2) Image Density A solid black image is produced using an image Neo Neo 450 manufactured by Ricoh, and the image density at any six positions of the image is measured with a Macbeth densitometer, and five levels are obtained from the average value of ID (image density). Five-level evaluation of 1 to 5 levels as the highest evaluation was performed. The image density of black toner using carbon black on the market is 2 levels.

(3) Background stain After outputting 1 million images, a white solid image is output, and the image density (ID) at any 6 positions of the image is measured with a Macbeth reflection densitometer. Five-level evaluation of 1 to 5 levels for evaluation was performed. The state where there is no background stain is a value equivalent to the reflection density of the paper. The larger the ID, the worse the background stain.

(4) Toner Scattering After outputting 1 million sheets of images, a five-level evaluation of 1 to 5 levels was performed, with 5 levels being the highest rating for the state of toner scattering inside the copying machine. Note that black toner using normal carbon black has two levels.

(5) Fine line reproducibility A 1-dot grid line image of 600 dots / inch and 150 line / inch was output in both the main scanning and sub-scanning directions, and the cut and blur of the line image were visually evaluated in five stages. Level 1 is the lowest rating and level 5 is the highest rating.
The evaluation results are shown in Table 3 below.

As is clear from the evaluation results in Table 3 above, in Examples 1 to 4 according to the present invention, high evaluation was obtained for all the evaluation items.
On the other hand, in Comparative Example 1 using the metal material 5 containing no titanium, the quality was slightly lowered with respect to the low-temperature fixability, the image density, and the background stain.
In Comparative Example 2 in which the content of the metal material 1 in the toner is less than 15% by weight, a reduction in image density was observed.
In Comparative Example 3 in which the content of the metal material 1 was more than 35% by weight and Comparative Example 4 using carbon black, the evaluation was low in most evaluation items.
In Comparative Example 5 using the toner 9 in which the content of the metal material 2 is less than 15% by weight, the image density was extremely low.
In Comparative Example 6 in which the toner 10 in which the content of the metal material 2 exceeds 35% by weight is extremely high, the evaluation was low in most evaluation items.

Claims (14)

A polymerized toner obtained by suspending a polymerizable monomer composition containing at least a polymerizable monomer and a black colorant in an aqueous dispersion medium and polymerizing using a polymerization initiator, Titanium having a saturation magnetization of 0.1 to 50 emu / g, a color system L ^* value of 9 to 15, and a ^* and b ^* both in the range of -1.0 to +1.0 as the black colorant A toner for developing an electrostatic charge image, comprising 15 to 35% by weight of a black iron oxide compound containing   The electrostatic image developing toner according to claim 1, wherein the black iron oxide compound contains 10 to 45% by weight of a titanium component in terms of Ti atoms with respect to Fe atoms. The toner for developing an electrostatic charge image according to claim 1, wherein the black iron oxide compound has a specific surface area of 1.3 to 80 m ² / g. 4. The electrostatic image developing toner according to claim 1, wherein the black iron oxide compound has a true specific gravity of 4.0 to 5.0 g / cm ³ .   5. The electrostatic image developing toner according to claim 1, wherein an average primary particle size of the black iron oxide compound is 0.05 to 2.0 μm.   6. The volume average particle size of toner particles is 3 to 8 μm, and the particle size ratio expressed by volume average particle size / number average particle size is 1.0 to 1.5. The toner for developing an electrostatic image according to any one of the above.   7. The electrostatic image developing toner according to claim 1, wherein the toner particles have an average circularity of 0.96 to 1.00.   8. The toner for developing an electrostatic charge image according to claim 1, further comprising a wax as a release agent.   The toner for developing an electrostatic charge image according to claim 1, further comprising a charge control agent.   A one-component developer comprising the electrostatic image developing toner according to any one of claims 1 to 9.   10. A two-component developer comprising the electrostatic image developing toner according to claim 1 and a carrier.   10. A toner container filled with the electrostatic image developing toner according to claim 1.   An image forming method using the toner for developing an electrostatic image according to claim 1. 12. A process cartridge for an image forming apparatus comprising at least an image carrier and a developing means, wherein the developer according to claim 10 or 11 is stored in the developing means. .