JP4319634B2 - Toner, method for producing the same, and image forming method - Google Patents

Description

  The present invention relates to a toner suitably used in an electrophotographic method, an electrostatic recording method, an electrostatic printing method, and the like, an efficient manufacturing method thereof, a developer using the toner, a container containing toner, a process cartridge, an image The present invention relates to a forming apparatus and an image forming method.

  Image formation by electrophotography generally forms an electrostatic image on a photoreceptor (electrostatic image carrier), develops the electrostatic image with a developer to form a visible image (toner image), The visible image is transferred to a recording medium such as paper and fixed to form a fixed image (see Patent Document 1).

  As the developer, a one-component developer using a magnetic toner or a non-magnetic toner alone and a two-component developer composed of a toner and a carrier are known. In general, a toner produced by a kneading and pulverizing method in which a thermoplastic resin is melt-kneaded with a colorant or the like, then finely pulverized, and further classified is used. If necessary, inorganic fine particles or organic fine particles may be added to the surface of the toner particles for the purpose of improving fluidity and cleaning properties.

The toner obtained by the kneading and pulverization method is generally fixed by heating and melting using a hot roll. At that time, if the hot roll temperature is too high, the toner is excessively melted and fused to the hot roll. An offset phenomenon may occur. Conversely, if the heat roll temperature is too low, the toner may not be sufficiently melted and fixing may be insufficient. In recent years, from the viewpoint of energy saving and downsizing of devices such as copying machines, a toner having both hot offset resistance and low temperature fixability that has a higher hot offset generation temperature and a lower fixing temperature has been demanded. In particular, in full-color copying machines, full-color printers, etc., the glossiness and color mixing of the image are important, so a toner having a lower melting point is desired. However, a toner having a lower melting point has a hot offset phenomenon. Since it tends to occur and is inferior in heat-resistant storage stability under high temperature and high humidity, a method for imparting releasability by applying silicone oil or the like to a hot roll has been conventionally employed in full-color equipment.
However, this method requires an oil tank, an oil application device, and the like, resulting in a complicated and large image forming apparatus. Moreover, since the deterioration of the heat roll is not likely to occur, maintenance is required every certain period. Furthermore, there is a problem that oil adheres to copy paper, OHP film, etc., and the color tone of the image deteriorates due to the adhered oil.

  Therefore, a method of adding a release agent such as wax to the toner is generally used in order to impart releasability without applying oil to the heat roll and prevent the problem of toner fusion. Here, the state of dispersion of the wax in the toner greatly affects the releasability. When the wax is compatible with the binder in the toner, the releasability cannot be expressed. At this time, if the dispersion diameter of the domain particles is too large, the ratio of the wax existing in the vicinity of the toner particle surface is relatively increased, so that the agglomeration is exhibited and the fluidity is deteriorated. There is a case where filming occurs due to transfer to a photoreceptor or the like, and good image quality cannot be obtained. On the other hand, if the dispersion diameter of the domain particles is too small, the wax may be excessively finely dispersed and sufficient releasability may not be obtained.

  In the pulverization and kneading method, it is difficult to control the dispersion diameter of the domain particles of the wax, and the wax is likely to be present on the fracture surface, so that more wax is exposed on the toner surface, resulting in poor fluidity and filming. The above-mentioned problems of generation of the above-mentioned may occur. Furthermore, the toner obtained by the pulverization and kneading method generally has a wide particle size distribution, unevenness in the triboelectric chargeability of the toner, and the occurrence of fog and the like. In addition, the volume average particle size is 2 to 2 in terms of production efficiency. There is a problem that it is difficult to obtain a toner having a small particle diameter of 8 μm and it is impossible to meet the demand for high image quality.

Therefore, attention is paid to toner obtained by granulation in an aqueous phase. The toner has a narrow particle size distribution, can be easily reduced in size, and can obtain a high-quality and high-definition image. Also excellent. In addition, the transfer uniformity is excellent due to the uniformity of charging, and the fluidity is good, and the design of the developing device is advantageous in that the design of the hopper and the torque for rotating the developing roll can be reduced. .
As a toner obtained by granulation in the aqueous phase, conventionally, a toner obtained by a suspension polymerization method or an emulsion polymerization aggregation method (hereinafter referred to as a chemical toner) has been developed.

In the suspension polymerization method, a monomer, a polymerization initiator, a colorant, a release agent, and the like are added to an aqueous phase containing a dispersion stabilizer while stirring to form oil droplets, and then the temperature is raised to cause a polymerization reaction. In this method, toner particles are obtained. According to the suspension polymerization method, although it is possible to reduce the toner particle size, it is necessary to use a dispersion stabilizer that lowers the chargeability when it remains, and if no dispersion stabilizer is used, There is a problem that it is difficult for the release agent to easily enter the oil droplets at the time of formation, and to be appropriately present on the surface of the toner particles.
The emulsion polymerization aggregation method uses, for example, a polyester resin as a binder resin, emulsified and dispersed in an aqueous phase, and then removed fine particles obtained by removing the solvent, a colorant, a release agent (wax), and the like. In this method, toner particles are produced by agglomerating a dispersion formed by dispersing in a phase and heating and fusing (see Patent Documents 2 to 3). According to these production methods, since there is no generation of ultrafine particles, it is possible to produce a classification-free toner with no emulsification loss and a sharp particle size distribution. If they are aggregated, the coalescence becomes insufficient, and cracks at the interface after the coalescence occur. For this reason, the heating process which advances coalescence between particles with heat is essential. However, when heated, bloom of the wax component finely dispersed in the toner particles (surface deposition) occurs or aggregation between the wax finely dispersed particles occurs, and the wax is maintained in a sufficiently finely dispersed state. I can't. In particular, when a wax having a low melting point (release agent) is used, there is a problem in that it is easy to dissolve in the heating process, the releasability cannot be ensured, and the oilless heat roll fixing is not suitable.

  Further, a release agent fine particle coated with or impregnated with a vinyl polymer by adding a polymerizable vinyl monomer and a water-soluble polymerization initiator to the release agent emulsion for polymerization is added at the time of emulsification of the toner composition. A method of uniformly and firmly adhering to the toner surface has been proposed (see Patent Document 4). However, in this method, it is essential to polymerize the release agent emulsion and the polymerizable vinyl monomer, and since the glass transition temperature (Tg) of the resin constituting the release agent fine particles is high, There exists a problem that it is inferior to releasability, low temperature fixability, etc.

  Therefore, while maintaining the advantages of a chemical toner that has a small particle size and narrow particle size distribution and excellent fluidity, it has excellent releasability at low temperatures, less filming, low temperature fixability and heat resistant storage stability. However, there is a strong demand for a method that can stably and efficiently obtain a toner capable of obtaining a high-quality image at the same time, but this method has not yet been provided.

US Pat. No. 2,297,691 JP-A-10-020552 JP 11-007156 A JP 2004-226669 A

  An object of the present invention is to solve various problems in the prior art and achieve the following objects. That is, the present invention is a toner having a small particle size and a narrow particle size distribution, which is excellent in releasability at low temperature, has little filming, achieves both low-temperature fixability and heat-resistant storage stability, and has high image quality. It is an object of the present invention to provide an efficient manufacturing method, and a developer, a container containing toner, a process cartridge, an image forming apparatus, and an image forming method capable of improving the image quality using the toner.

  As a result of intensive studies in view of the above problems, the present inventors have obtained the following knowledge. That is, a solution or dispersion of the toner material prepared by dissolving or dispersing the toner material in an organic solvent is dispersed as dispersed particles in an aqueous medium to prepare an oil-in-water type dispersion, and the oil-in-water type By dispersing the aqueous dispersion of wax in the dispersion and granulating the toner, it is possible to uniformly disperse the wax particles having a small particle diameter in the toner without using a dispersant, etc. It has been found that a toner can be obtained that prevents the wax from being unevenly distributed in the toner particles, has excellent releasability, and generates less filming. In addition, since no heating is required in the toner manufacturing process, a wax having a low melting point can be used, it is excellent in releasability at low temperature, and both low-temperature fixability and heat-resistant storage stability are achieved. The present inventors have found that a toner having a small particle size and a narrow particle size distribution can be obtained.

The present invention is based on the above findings of the present inventors, and means for solving the above problems are as follows. That is,
<1> A toner material is dissolved or dispersed in an organic solvent to prepare a solution or dispersion of the toner material, and the dissolved or dispersed liquid is dispersed as dispersed particles in an aqueous medium that does not contain organic resin fine particles. After preparing an oil droplet type dispersion, an aqueous wax dispersion and organic resin fine particles are added to the oil-in-water dispersion, and the toner is granulated in the presence of the organic resin fine particles. A toner manufacturing method.
<2> A toner material is dissolved or dispersed in an organic solvent to prepare a solution or dispersion of the toner material, and the dissolved or dispersed liquid is dispersed as a dispersed particle having a volume average particle size of 0.1 to 3 μm in an aqueous medium. After preparing an oil-in-water dispersion by dispersion, a water dispersion of wax is added to the oil-in-water dispersion, and the volume average particle diameter of the dispersion is increased to 3 to 9 μm before the toner Is a method for producing a toner.
<3> A toner material is dissolved or dispersed in an organic solvent to prepare a solution or dispersion of the toner material, and the dissolved or dispersed solution has a volume average particle size of 0.00 in an aqueous medium containing no organic resin fine particles. After preparing an oil-in-water dispersion by dispersing as dispersed particles of 1 to 3 μm, an aqueous dispersion of wax and organic resin fine particles are added to the oil-in-water dispersion and in the presence of the organic resin fine particles. The toner is granulated after increasing the volume average particle size of the dispersed particles to 3 to 9 μm.
<4> Dissolve or disperse the toner material in an organic solvent to prepare a solution or dispersion of the toner material, and disperse the disperse or disperse as dispersed particles in an aqueous medium to prepare an oil-in-water dispersion. Then, a water dispersion of wax is added to the oil-in-water dispersion, and the toner is granulated after increasing the volume average particle size of the dispersed particles by 3 to 45 times. It is a manufacturing method.
<5> The toner according to <4>, wherein the volume average particle diameter of the dispersed particles before the increase is 0.1 to 3 μm, and the volume average particle diameter of the dispersed particles after the increase is 3 to 9 μm. It is a manufacturing method.
<6> The water dispersion of the wax and the organic resin fine particles are prepared in the order of the water dispersion of the wax and the organic resin fine particles in this order after preparing the oil-in-water dispersion. The method for producing a toner according to any one of the above.
<7> The method for producing a toner according to any one of <1> to <6>, wherein the volume average particle diameter of the dispersed particles of the wax in the aqueous dispersion of wax is 0.1 to 2 μm.
<8> The method for producing a toner according to any one of <1> to <7>, wherein the solution or dispersion of the toner material contains a wax, and the wax is dispersed in the solution or dispersion.
<9> The method for producing a toner according to any one of <1> to <8>, wherein the wax has a melting point of 50 to 90 ° C.
<10> The method for producing a toner according to any one of <1> to <9>, wherein the wax is paraffin wax.
<11> The method for producing a toner according to any one of <1> and <3>, wherein an ionizing agent is added together with the organic resin fine particles when the organic resin fine particles are added.
<12> The method for producing a toner according to any one of <2> and <4> to <11>, wherein an ionizing agent is added when the volume average particle diameter of the dispersed particles is increased.
<13> The method for producing a toner according to any one of <11> to <12>, wherein the ionizing agent is at least one selected from a salt composed of a monovalent cation and a monovalent anion. is there.
<14> The method for producing a toner according to <13>, wherein the monovalent cation includes at least one of a sodium ion and a potassium ion.
<15> The method for producing a toner according to any one of <1> to <14>, wherein the solution or dispersion of the toner material is dispersed in an aqueous medium while stirring.
<16> When the stirring speed when dissolving the toner material or dispersing the dispersion in the aqueous medium is Am / s, and the stirring speed when granulating the toner is Bm / s, The toner production method according to any one of <1> to <15>, wherein <A <23 and 1.4 <A / B <100 are satisfied.
<17> The toner production method according to any one of <2> to <16>, wherein the volume average particle diameter of the dispersed particles before the increase is 0.1 to 2 μm.
<18> The toner material includes at least an active hydrogen group-containing compound and a polymer capable of reacting with the active hydrogen group-containing compound,
By granulating, by reacting the active hydrogen group-containing compound and a polymer capable of reacting with the active hydrogen group-containing compound to produce an adhesive base material, particles containing at least the adhesive base material are obtained. The method for producing a toner according to any one of <1> to <17>, wherein the toner is produced.

<19> A toner produced by the method for producing a toner according to any one of <1> to <18>.
<20> The toner according to <19>, wherein the adhesive base material includes a polyester resin.
<21> The toner according to <20>, wherein the molecular weight distribution of the polyester resin-soluble tetrahydrofuran (THF) is 1,000 to 30,000 in terms of weight average molecular weight (Mw).
<22> The toner according to any one of <20> to <21>, wherein the acid value of the polyester resin is 1.0 to 50.0 (KOH mg / g).
<23> The toner according to any one of <20> to <22>, wherein the glass transition temperature (Tg) of the polyester resin is 35 to 70 ° C.
<24> The toner according to any one of <19> to <23>, wherein the toner has a volume average particle diameter of 3 to 9 μm.
<25> The toner according to any one of <19> to <24>, wherein the toner has a volume average particle diameter (Dv) / number average particle diameter (Dn) of 1.05 to 1.25.
<26> The toner according to any one of <19> to <25>, wherein the toner has a glass transition temperature (Tg) of 40 to 70 ° C.
<27> The toner according to any one of <19> to <26>, wherein the toner has an acid value of 0.5 to 40.0 (KOH mg / g).

<28> A developer comprising the toner according to any one of <19> to <27>.
<29> A toner-containing container filled with the toner according to any one of <19> to <27>.
<30> An electrostatic latent image carrier and an electrostatic latent image formed on the electrostatic latent image carrier are developed using the toner according to any one of <19> to <27> to be a visible image And a developing means for forming the process cartridge.
<31> An electrostatic latent image carrier, electrostatic latent image forming means for forming an electrostatic latent image on the electrostatic latent image carrier, and the electrostatic latent image according to <19> to <27> Developing means for developing a visible image by developing using any of the toners, Transfer means for transferring the visible image to a recording medium, Fixing means for fixing the transferred image transferred to the recording medium, The image forming apparatus is characterized by having at least.
<32> An electrostatic latent image forming step of forming an electrostatic latent image on the electrostatic latent image carrier, and using the toner according to any one of <19> to <27>, An image comprising at least a developing step for developing to form a visible image, a transferring step for transferring the visible image to a recording medium, and a fixing step for fixing the transferred image transferred to the recording medium It is a forming method.

  The first toner production method of the present invention comprises dissolving or dispersing a toner material in an organic solvent to prepare a solution or dispersion of the toner material, and using the solution or dispersion as an aqueous medium not containing organic resin fine particles. After preparing an oil-in-water dispersion by dispersing as dispersed particles therein, a water dispersion of wax and organic resin fine particles are added to the oil-in-water dispersion and toner is added in the presence of the organic resin fine particles. It is characterized by granulating. In the toner manufacturing method, the toner material is dissolved or dispersed in an organic solvent to prepare a solution or dispersion of the toner material. The dissolved or dispersed liquid is dispersed as dispersed particles in an aqueous medium not containing organic resin fine particles to prepare an oil-in-water dispersion. An aqueous dispersion of wax and organic resin fine particles are added to the oil-in-water dispersion and the toner is granulated in the presence of the organic resin fine particles. As a result, it is possible to uniformly disperse the wax particles having a small particle diameter in the toner without causing the use of a dispersant or the like, and to appropriately exist on the toner surface, thereby preventing uneven distribution of the wax in the toner particles. In addition, a toner that is excellent in releasability, has little filming, and can obtain high image quality is efficiently produced. In the method for producing the toner, since heating is not necessary, a wax having a low melting point can be used, and the releasability at low temperature is excellent, and both low-temperature fixability and heat-resistant storage stability are achieved. Further, the organic resin fine particles are not used at the time of preparing the oil-in-water dispersion, and the organic resin fine particles are used at the time of granulating the toner, whereby a toner having a small particle size and a narrow particle size distribution can be obtained.

  In the second method for producing a toner of the present invention, a toner material is dissolved or dispersed in an organic solvent to prepare a solution or dispersion of the toner material, and the dissolved or dispersed solution has a volume average particle diameter in an aqueous medium. After preparing an oil-in-water dispersion by dispersing as 0.1 to 3 μm dispersed particles, an aqueous dispersion of wax is added to the oil-in-water dispersion, and the volume average particle size of the dispersed particles is determined. The toner is granulated after increasing to 3 to 9 μm. In the toner manufacturing method, the toner material is dissolved or dispersed in the organic solvent to prepare a solution or dispersion of the toner material. The dissolved or dispersed liquid is dispersed as dispersed particles having a volume average particle diameter of 0.1 to 3 μm in the aqueous medium to prepare the oil-in-water dispersion. An aqueous dispersion of wax is added to the oil-in-water dispersion, and the volume average particle size of the dispersed particles is increased to 3 to 9 μm before granulating the toner. As a result, it is possible to efficiently produce a toner having excellent releasability at low temperature, little filming, low temperature fixability and heat resistant storage stability, and high image quality. In the toner production method, the dispersed particles having a volume average particle diameter of 0.1 to 3 μm are formed, and the toner is granulated after increasing the volume average particle diameter of the dispersed particles to 3 to 9 μm. Therefore, a toner having a uniform material composition among the toner particles, excellent chargeability, fixability and the like, a small particle size and a narrow particle size distribution can be obtained.

  The third method for producing a toner of the present invention comprises dissolving or dispersing a toner material in an organic solvent to prepare a dissolved or dispersed solution of the toner material, and using the dissolved or dispersed solution as an aqueous medium not containing organic resin fine particles. After preparing an oil-in-water dispersion by dispersing it as dispersed particles having a volume average particle size of 0.1 to 3 μm, an aqueous wax dispersion and organic resin fine particles are added to the oil-in-water dispersion Then, the toner is granulated after the volume average particle diameter of the dispersed particles is increased to 3 to 9 μm in the presence of the organic resin fine particles. As a result, a toner with small particle size and narrow particle size distribution that is excellent in releasability at low temperature, has less filming, achieves both high-temperature fixability and heat-resistant storage stability, and has high image quality can be efficiently produced. can get. Further, the obtained toner has a uniform material composition among toner particles, and is excellent in chargeability, fixability and the like.

  According to a fourth method for producing a toner of the present invention, a toner material is dissolved or dispersed in an organic solvent to prepare a solution or dispersion of the toner material, and the dissolved or dispersed liquid is dispersed as dispersed particles in an aqueous medium. After preparing an oil-in-water dispersion, an aqueous wax dispersion is added to the oil-in-water dispersion, and the volume average particle size of the dispersed particles is increased by 3 to 45 times. It is characterized by granulation. In the toner manufacturing method, the toner material is dissolved or dispersed in the organic solvent to prepare a solution or dispersion of the toner material. The dissolved or dispersed liquid is dispersed as dispersed particles in the aqueous medium to prepare the oil-in-water dispersion. An aqueous dispersion of the wax is added to the oil-in-water dispersion, and the toner is granulated after the volume average particle diameter of the dispersed particles is increased by 3 to 45 times. As a result, it is possible to efficiently produce a toner having excellent releasability at low temperature, little filming, low temperature fixability and heat resistant storage stability, and high image quality. In the toner production method, after forming dispersed particles having a small diameter, the toner is granulated after increasing the volume average particle size of the dispersed particles to 3 to 45 times, so that the composition of the material between the toner particles Is uniform, excellent in charging property, fixing property, etc., and a toner having a small particle size and a narrow particle size distribution can be obtained.

The toner material includes at least an active hydrogen group-containing compound and a polymer capable of reacting with the active hydrogen group-containing compound, and the granulation includes the active hydrogen group-containing compound and the active hydrogen group-containing compound. And a polymer capable of reacting with each other to produce particles having at least the adhesive substrate while producing an adhesive substrate. A toner that is excellent in various properties such as moldability and fixability, in particular, low-temperature fixability and can obtain high image quality is efficiently produced.
In addition, an aspect in which the volume average particle diameter of the wax dispersion particles in the aqueous dispersion of wax is 0.1 to 2 μm, an aspect in which the melting point of the wax is 50 to 90 ° C., and an aspect in which the wax is paraffin wax. Are preferable.

  The toner of the present invention is produced by the toner production method of the present invention. For this reason, the toner has a small particle size and a narrow particle size distribution, is excellent in releasability at low temperatures, has little filming, and has both low-temperature fixability and heat-resistant storage stability, and can provide high image quality. Further, when the toner contains particles containing at least an adhesive substrate obtained by reacting the active hydrogen group-containing compound with a polymer capable of reacting with the active hydrogen group-containing compound, anti-aggregation property, charging property, fluidity, releasability Excellent properties such as fixing properties. When image formation is performed using the toner, high image quality can be obtained under low-temperature fixing conditions.

  The developer of the present invention contains the toner of the present invention. For this reason, when an image is formed by electrophotography using the developer, a high-quality image with high image density and high sharpness is formed.

  The toner container of the present invention is filled with the toner of the present invention. For this reason, when an image is formed by electrophotography using the toner of the present invention filled in the toner-containing container, a high-quality image with high image density and high sharpness is formed.

  The process cartridge of the present invention comprises an electrostatic latent image carrier, and developing means for developing the electrostatic latent image formed on the electrostatic latent image carrier using the toner of the present invention to form a visible image. At least. The process cartridge is detachable from the image forming apparatus, is excellent in convenience, and uses the toner of the present invention, so that a high quality image with high image density and high sharpness can be formed.

  The image forming apparatus of the present invention includes an electrostatic latent image carrier, electrostatic latent image forming means for forming an electrostatic latent image on the electrostatic latent image carrier, and the electrostatic latent image of the present invention. The image forming apparatus includes at least a developing unit that forms a visible image by developing with toner, a transfer unit that transfers the visible image to a recording medium, and a fixing unit that fixes the transferred image transferred to the recording medium. In the image forming apparatus, the electrostatic latent image forming unit forms an electrostatic latent image on the electrostatic latent image carrier. The developing means develops the electrostatic latent image using the toner of the present invention to form a visible image. The transfer means transfers the visible image to a recording medium. The fixing unit fixes the transferred image transferred to the recording medium. As a result, a high-quality image with high image density and high sharpness is formed.

  The image forming method of the present invention comprises an electrostatic latent image forming step of forming an electrostatic latent image on an electrostatic latent image carrier, and developing the electrostatic latent image with the toner of the present invention to make visible. It includes at least a developing step for forming an image, a transfer step for transferring the visible image to a recording medium, and a fixing step for fixing the transferred image transferred to the recording medium. In the image forming apparatus, an electrostatic latent image is formed on the electrostatic latent image carrier in the electrostatic latent image forming step. In the developing step, the electrostatic latent image is developed using the toner of the present invention to form a visible image. In the transfer step, the visible image is transferred to a recording medium. In the fixing step, the transferred image transferred to the recording medium is fixed. As a result, a high-quality image with high image density and high sharpness is formed.

  According to the present invention, the conventional problems can be solved, the releasability at low temperature is excellent, the filming on the photoconductor is small, the low temperature fixability and the heat resistant storage stability are compatible, and the high image quality. , A toner having a small particle size and a narrow particle size distribution, and an efficient manufacturing method thereof, and a developer, a container containing toner, a process cartridge, an image forming apparatus, and an image, which can be used to improve image quality using the toner A forming method can be provided.

(Toner and toner production method)
The method for producing a toner of the present invention comprises an oil-in-water dispersion type preparation step of preparing an oil-in-water dispersion by dispersing a dispersion or dispersion of a toner material as dispersed particles in an aqueous medium, and the oil-in-water droplets described above. A toner granulation step of granulating the toner by adding at least an aqueous wax dispersion to the mold dispersion, and further including other steps as necessary. Specific examples of the method for producing the toner include the following embodiments.
According to a first aspect of the method for producing a toner of the present invention, a toner material is dissolved or dispersed, and the dissolved or dispersed liquid is dispersed as dispersed particles in an aqueous medium not containing organic resin fine particles. After preparing the drop dispersion, an aqueous wax dispersion and organic resin fine particles are added to the oil-in-water dispersion, and the toner is granulated in the presence of the organic resin fine particles.
According to a second aspect of the method for producing a toner of the present invention, a toner material is dissolved or dispersed, and the dissolved or dispersed liquid is dispersed in an aqueous medium with a volume average particle size of 0.1 to 3 μm. After preparing an oil-in-water dispersion by dispersion, a water dispersion of wax is added to the oil-in-water dispersion, and the volume average particle diameter of the dispersed particles is increased to 3 to 9 μm. Granulate.
According to a third aspect of the method for producing a toner of the present invention, a toner material is dissolved or dispersed in the aqueous medium containing no organic resin fine particles. After preparing an oil-in-water dispersion by dispersing as dispersed particles of ˜3 μm, an aqueous wax dispersion and organic resin fine particles are added to the oil-in-water dispersion, and in the presence of the organic resin fine particles. The toner is granulated after increasing the volume average particle size of the dispersed particles to 3 to 9 μm.
According to a fourth aspect of the method for producing a toner of the present invention, an oil-in-water dispersion is prepared by preparing a solution or dispersion of a toner material and dispersing the solution or dispersion as dispersed particles in an aqueous medium. Thereafter, an aqueous dispersion of wax is added to the oil-in-water dispersion, and the volume average particle size of the dispersed particles is increased by 3 to 45 times before granulating the toner.

The toner of the present invention is obtained by the toner production method of the present invention.
In a preferred embodiment of the toner of the present invention, the toner material includes at least an active hydrogen group-containing compound and a polymer capable of reacting with the active hydrogen group-containing compound, and the granulation includes the active hydrogen group-containing compound. And a toner that is produced by reacting a polymer capable of reacting with the active hydrogen group-containing compound to produce an adhesive base material, and obtaining particles containing at least the adhesive base material. .
Hereinafter, the details of the toner of the present invention will be clarified through the description of the toner production method of the present invention.

<Oil-in-water dispersion preparation process>
The oil-in-water dispersion preparation step is a step of preparing an oil-in-water dispersion by dispersing the toner material dissolution or dispersion as dispersed particles in an aqueous medium.
In the method for producing the toner according to the first and third aspects of the present invention, it is necessary to form the dispersed particles in an aqueous medium that does not contain organic resin fine particles. Since the organic resin fine particles are generally used for the purpose of controlling the toner shape (average circularity, particle size distribution, etc.), when the aqueous medium contains organic resin fine particles, at the same time as the formation of the dispersed particles, Integration of the dispersed particles located in the vicinity may progress and fine dispersed particles may not be obtained, and it is difficult to adjust the desired particle size distribution, toner shape, reaction control, uneven distribution of materials in the toner particles, etc. It may become.

-Dissolution or dispersion of toner material-
The solution or dispersion of the toner material is obtained by dissolving or dispersing the toner material in an organic solvent.
The toner material is not particularly limited as long as the toner can be formed, and can be appropriately selected according to the purpose. For example, the monomer, the polymer, the active hydrogen group-containing compound, and the reaction with the active hydrogen group-containing compound can be selected. It contains at least one of the possible polymers (prepolymers), and further contains other components such as a colorant and a charge control agent as necessary.
In the toner production method of the preferred embodiment of the present invention, the toner material can be dissolved or dispersed in the organic solvent so that it can react with the active hydrogen group-containing compound and the active hydrogen group-containing compound. A toner material such as a polymer, the colorant, and the charge control agent can be dissolved or dispersed, and the polymer (pre-polymer) that can react with the active hydrogen group-containing compound in the toner material. Components other than the polymer) may be added and mixed in the aqueous medium in the preparation of the aqueous medium described later, or the dissolution or dispersion of the toner material is added to the aqueous medium. Or you may add to the said aqueous medium with a dispersion liquid.

The organic solvent is not particularly limited as long as it is a solvent that can dissolve or disperse the toner material, and can be appropriately selected according to the purpose. For example, the boiling point is less than 150 ° C. in terms of ease of removal. Volatile ones are preferred, for example, toluene, xylene, benzene, carbon tetrachloride, methylene chloride, 1,2-dichloroethane, 1,1,2-trichloroethane, trichloroethylene, chloroform, monochlorobenzene, dichloroethylidene, methyl acetate, acetic acid Examples include ethyl, methyl ethyl ketone, and methyl isobutyl ketone. Among these, toluene, xylene, benzene, methylene chloride, 1,2-dichloroethane, chloroform, carbon tetrachloride and the like are preferable, and ethyl acetate is particularly preferable. These may be used individually by 1 type and may use 2 or more types together.
There is no restriction | limiting in particular as the usage-amount of the said organic solvent, According to the objective, it can select suitably, For example, 40-300 mass parts is preferable with respect to 100 mass parts of said toner materials, and 60-140 mass parts is preferable. More preferably, 80-120 mass parts is still more preferable.

-Active hydrogen group-containing compound-
The active hydrogen group-containing compound acts as an elongation agent, a crosslinking agent, or the like when a polymer capable of reacting with the active hydrogen group-containing compound undergoes an elongation reaction, a crosslinking reaction, or the like in the aqueous phase.
The active hydrogen group-containing compound is not particularly limited as long as it has an active hydrogen group, and can be appropriately selected depending on the purpose. For example, the polymer capable of reacting with the active hydrogen group-containing compound is In the case of the isocyanate group-containing polyester prepolymer (A), the amines (B) can be increased in molecular weight by a reaction such as an elongation reaction or a crosslinking reaction with the isocyanate group-containing polyester prepolymer (A). Is preferred.
There is no restriction | limiting in particular as said active hydrogen group, According to the objective, it can select suitably, For example, a hydroxyl group (alcoholic hydroxyl group or phenolic hydroxyl group), an amino group, a carboxyl group, a mercapto group etc. are mentioned. These may be used individually by 1 type and may use 2 or more types together. Among these, an alcoholic hydroxyl group is particularly preferable.

The amines (B) are not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include diamine (B1), trivalent or higher polyamine (B2), amino alcohol (B3), and amino mercaptan. (B4), amino acid (B5), and those obtained by blocking the amino groups of B1 to B5 (B6).
These may be used individually by 1 type and may use 2 or more types together. Among these, diamine (B1), a mixture of diamine (B1) and a small amount of a trivalent or higher polyamine (B2) are particularly preferable.

Examples of the diamine (B1) include aromatic diamines, alicyclic diamines, and aliphatic diamines. Examples of the aromatic diamine include phenylenediamine, diethyltoluenediamine, 4,4′diaminodiphenylmethane, and the like. Examples of the alicyclic diamine include 4,4′-diamino-3,3′dimethyldicyclohexylmethane, diaminecyclohexane, and isophoronediamine. Examples of the aliphatic diamine include ethylene diamine, tetramethylene diamine, and hexamethylene diamine.
Examples of the trivalent or higher polyamine (B2) include diethylenetriamine and triethylenetetramine.
Examples of the amino alcohol (B3) include ethanolamine and hydroxyethylaniline.
Examples of the amino mercaptan (B4) include aminoethyl mercaptan and aminopropyl mercaptan.
Examples of the amino acid (B5) include aminopropionic acid and aminocaproic acid.
Examples of the block (B6) in which the amino group of B1 to B5 is blocked include, for example, a ketimine obtained from any of the amines (B1) to (B5) and ketones (acetone, methyl ethyl ketone, methyl isobutyl ketone, etc.) Compounds, oxazolyzone compounds, and the like.

In the extension reaction or crosslinking reaction between the active hydrogen group-containing compound and the polymer capable of reacting with the active hydrogen group-containing compound, it is preferable to use a reaction aid (catalyst) for the extension reaction or the crosslinking reaction. . Examples of the catalyst include tertiary amine compounds.
There is no restriction | limiting in particular as said tertiary amine compound, Although it can select suitably according to the objective, For example, the compound represented by following General formula (1) is mentioned suitably. The tertiary amine compound not only functions as a catalyst, but also functions as an emulsification aid when the toner material is dissolved or dispersed in the aqueous medium in the preparation of the oil-in-water dispersion. This is preferable.

  A reaction terminator can be used to stop the elongation reaction, the crosslinking reaction, etc. between the active hydrogen group-containing compound and the polymer capable of reacting with the active hydrogen group-containing compound. Use of the reaction terminator is preferable in that the molecular weight and the like of the adhesive substrate can be controlled within a desired range. Examples of the reaction terminator include monoamines (diethylamine, dibutylamine, butylamine, laurylamine, etc.) or those blocked (ketimine compounds).

As a mixing ratio of the amines (B) and the isocyanate group-containing polyester prepolymer (A), the isocyanate group [NCO] in the isocyanate group-containing prepolymer (A) and the amines (B) The mixing equivalent ratio ([NCO] / [NHx]) of the amino group [NHx] is preferably 1/3 to 3/1, more preferably 1/2 to 2/1, It is particularly preferably 1.5 to 1.5 / 1.
When the mixing equivalent ratio ([NCO] / [NHx]) is less than 1/3, the low-temperature fixability may be lowered. When the mixing equivalent ratio exceeds 3/1, the molecular weight of the urea-modified polyester resin becomes low. The hot offset resistance may be deteriorated.

--Polymer capable of reacting with active hydrogen group-containing compound--
The polymer capable of reacting with the active hydrogen group-containing compound (hereinafter sometimes referred to as “prepolymer”) is not particularly limited as long as it has at least a site capable of reacting with the active hydrogen group-containing compound. However, it can be appropriately selected from known resins, and examples thereof include polyol resins, polyacrylic resins, polyester resins, epoxy resins, and derivative resins thereof.
These may be used individually by 1 type and may use 2 or more types together. Among these, a polyester resin is particularly preferable in terms of high fluidity and transparency during melting.

The site capable of reacting with the active hydrogen group-containing compound in the prepolymer is not particularly limited and may be appropriately selected from known substituents. For example, an isocyanate group, an epoxy group, a carboxylic acid, An acid chloride group, and the like.
These may be contained singly or in combination of two or more. Among these, an isocyanate group is particularly preferable.

Among the prepolymers, it is easy to adjust the molecular weight of the polymer component, and oil-less low-temperature fixing characteristics in dry toners, in particular, good releasability and fixability even in the absence of a release oil application mechanism to a heating medium for fixing. It is particularly preferable that it is a urea bond-forming group-containing polyester resin (RMPE) in that it can be secured.
As said urea bond production | generation group, an isocyanate group etc. are mentioned, for example. When the urea bond-forming group in the urea bond-forming group-containing polyester resin (RMPE) is the isocyanate group, the isocyanate group-containing polyester prepolymer (A) and the like are particularly preferable as the polyester resin (RMPE). It is done.

  The isocyanate group-containing polyester prepolymer (A) is not particularly limited and may be appropriately selected depending on the intended purpose. For example, it is a polycondensate of a polyol (PO) and a polycarboxylic acid (PC), And what made the said active hydrogen group containing polyester resin react with polyisocyanate (PIC), etc. are mentioned.

  There is no restriction | limiting in particular as said polyol (PO), According to the objective, it can select suitably, For example, diol (DIO), trihydric or more polyol (TO), diol (DIO), and trihydric or more polyol A mixture with (TO), etc. are mentioned. These may be used individually by 1 type and may use 2 or more types together. Among these, the diol (DIO) alone or a mixture of the diol (DIO) and a small amount of the trivalent or higher polyol (TO) is preferable.

Examples of the diol (DIO) include alkylene glycol, alkylene ether glycol, alicyclic diol, alkylene oxide adduct of alicyclic diol, bisphenol, alkylene oxide adduct of bisphenol, and the like.
The alkylene glycol is preferably one having 2 to 12 carbon atoms, such as ethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, 1,4-butanediol, 1,6-hexanediol, and the like. Can be mentioned. Examples of the alkylene ether glycol include diethylene glycol, triethylene glycol, dipropylene glycol, polyethylene glycol, polypropylene glycol, and polytetramethylene ether glycol. Examples of the alicyclic diol include 1,4-cyclohexanedimethanol and hydrogenated bisphenol A. Examples of the alkylene oxide adduct of the alicyclic diol include those obtained by adding an alkylene oxide such as ethylene oxide, propylene oxide, butylene oxide to the alicyclic diol. Examples of the bisphenols include bisphenol A, bisphenol F, and bisphenol S. Examples of the alkylene oxide adduct of the bisphenol include those obtained by adding an alkylene oxide such as ethylene oxide, propylene oxide, butylene oxide to the bisphenol.
Among these, alkylene glycols having 2 to 12 carbon atoms, alkylene oxide adducts of bisphenols, and the like are preferable. Mixtures are particularly preferred.

As the trivalent or higher polyol (TO), those having 3 to 8 or higher valences are preferable. And alkylene oxide adducts.
Examples of the trihydric or higher polyhydric aliphatic alcohol include glycerin, trimethylolethane, trimethylolpropane, pentaerythritol, sorbitol and the like. Examples of the trihydric or higher polyphenols include trisphenol PA, phenol novolak, cresol novolak, and the like. Examples of the trivalent or higher polyphenols alkylene oxide adducts include those obtained by adding an alkylene oxide such as ethylene oxide, propylene oxide, butylene oxide to the trivalent or higher polyphenols.

  The mixture mass ratio (DIO: TO) of the diol (DIO) and the trivalent or higher polyol (TO) in the mixture of the diol (DIO) and the trivalent or higher polyol (TO) is 100: 0.01-10 are preferable and 100: 0.01-1 are more preferable.

There is no restriction | limiting in particular as said polycarboxylic acid (PC), Although it can select suitably according to the objective, For example, dicarboxylic acid (DIC), trivalent or more polycarboxylic acid (TC), dicarboxylic acid (DIC) ) And a tricarboxylic or higher polycarboxylic acid.
These may be used individually by 1 type and may use 2 or more types together. Among these, dicarboxylic acid (DIC) alone or a mixture of DIC and a small amount of trivalent or higher polycarboxylic acid (TC) is preferable.
Examples of the dicarboxylic acid include alkylene dicarboxylic acid, alkenylene dicarboxylic acid, aromatic dicarboxylic acid, and the like.
Examples of the alkylene dicarboxylic acid include succinic acid, adipic acid, sebacic acid, and the like. As said alkenylene dicarboxylic acid, a C4-C20 thing is preferable, For example, a maleic acid, a fumaric acid, etc. are mentioned. As said aromatic dicarboxylic acid, a C8-C20 thing is preferable, For example, a phthalic acid, isophthalic acid, a terephthalic acid, naphthalene dicarboxylic acid etc. are mentioned.
Among these, alkenylene dicarboxylic acid having 4 to 20 carbon atoms and aromatic dicarboxylic acid having 8 to 20 carbon atoms are preferable.

The trivalent or higher polycarboxylic acid (TO) is preferably 3 to 8 or higher, and examples thereof include aromatic polycarboxylic acids.
As said aromatic polycarboxylic acid, a C9-C20 thing is preferable, For example, trimellitic acid, pyromellitic acid, etc. are mentioned.

  As the polycarboxylic acid (PC), the dicarboxylic acid (DIC), the trivalent or higher polycarboxylic acid (TC), and a mixture of the dicarboxylic acid (DIC) and the trivalent or higher polycarboxylic acid, Any acid anhydride or lower alkyl ester selected from can also be used. Examples of the lower alkyl ester include methyl ester, ethyl ester, isopropyl ester and the like.

  Mixing mass ratio (DIC: TC) of the dicarboxylic acid (DIC) and the trivalent or higher polycarboxylic acid (TC) in the mixture of the dicarboxylic acid (DIC) and the trivalent or higher polycarboxylic acid (TC) There is no restriction | limiting in particular, According to the objective, it can select suitably, For example, 100: 0.01-10 are preferable and 100: 0.01-1 are more preferable.

  The mixing ratio for the polycondensation reaction between the polyol (PO) and the polycarboxylic acid (PC) is not particularly limited and may be appropriately selected depending on the intended purpose. For example, in the polyol (PO) The equivalent ratio ([OH] / [COOH]) of the hydroxyl group [OH] to the carboxyl group [COOH] in the polycarboxylic acid (PC) is usually preferably 2/1 to 1/1. More preferably, it is 0.5 / 1 to 1/1, and particularly preferably 1.3 / 1 to 1.02 / 1.

There is no restriction | limiting in particular as content in the said isocyanate group containing polyester prepolymer (A) of the said polyol (PO), Although it can select suitably according to the objective, For example, 0.5-40 mass% is preferable. 1-30 mass% is more preferable, and 2-20 mass% is especially preferable.
When the content is less than 0.5% by mass, the hot offset resistance deteriorates, and it may be difficult to achieve both the heat-resistant storage stability and the low-temperature fixability of the toner, and exceeds 40% by mass. In some cases, the low-temperature fixability may deteriorate.

The polyisocyanate (PIC) is not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include aliphatic polyisocyanates, alicyclic polyisocyanates, aromatic diisocyanates, araliphatic diisocyanates, and isocyanurates. And those blocked with phenol derivatives, oximes, caprolactams, and the like.
Examples of the aliphatic polyisocyanate include tetramethylene diisocyanate, hexamethylene diisocyanate, 2,6-diisocyanatomethylcaproate, octamethylene diisocyanate, decamethylene diisocyanate, dodecamethylene diisocyanate, tetradecamethylene diisocyanate, trimethylhexane diisocyanate, Examples include tetramethylhexane diisocyanate. Examples of the alicyclic polyisocyanate include isophorone diisocyanate and cyclohexylmethane diisocyanate. Examples of the aromatic diisocyanate include tolylene diisocyanate, diphenylmethane diisocyanate, 1,5-naphthylene diisocyanate, diphenylene-4,4′-diisocyanate, 4,4′-diisocyanato-3,3′-dimethyldiphenyl, 3- Examples thereof include methyldiphenylmethane-4,4′-diisocyanate, diphenyl ether-4,4′-diisocyanate and the like. Examples of the araliphatic diisocyanate include α, α, α ′, α′-tetramethylxylylene diisocyanate. Examples of the isocyanurates include tris-isocyanatoalkyl-isocyanurate and triisocyanatocycloalkyl-isocyanurate.
These can be used alone or in combination of two or more.

As a mixing ratio when the polyisocyanate (PIC) and the active hydrogen group-containing polyester resin (for example, a hydroxyl group-containing polyester resin) are reacted, the isocyanate group [NCO] in the polyisocyanate (PIC) and the hydroxyl group-containing group are used. The mixing equivalent ratio ([NCO] / [OH]) with the hydroxyl group [OH] in the polyester resin is usually preferably 5/1 to 1/1, and preferably 4/1 to 1.2 / 1. More preferred is 3/1 to 1.5 / 1.
When the isocyanate group [NCO] exceeds 5, low-temperature fixability may be deteriorated, and when it is less than 1, offset resistance may be deteriorated.

There is no restriction | limiting in particular as content in the said isocyanate group containing polyester prepolymer (A) of the said polyisocyanate (PIC), Although it can select suitably according to the objective, For example, 0.5-40 mass% is Preferably, 1-30 mass% is more preferable, and 2-20 mass% is still more preferable.
When the content is less than 0.5% by mass, the hot offset resistance is deteriorated, and it may be difficult to achieve both heat-resistant storage stability and low-temperature fixability. When the content exceeds 40% by mass, Low temperature fixability may deteriorate.

As an average number of the isocyanate groups contained per molecule of the isocyanate group-containing polyester prepolymer (A), 1 or more is preferable, 1.2 to 5 is more preferable, and 1.5 to 4 is more preferable.
When the average number of the isocyanate groups is less than 1, the molecular weight of the polyester resin (RMPE) modified with the urea bond-forming group is lowered, and the hot offset resistance may be deteriorated.

  The weight average molecular weight (Mw) of the polymer capable of reacting with the active hydrogen group-containing compound is 3,000 to 40,000 in terms of molecular weight distribution by GPC (gel permeation chromatography) soluble in tetrahydrofuran (THF). Preferably, 4,000 to 30,000 is more preferable. When the weight average molecular weight (Mw) is less than 3,000, the heat resistant storage stability may be deteriorated, and when it exceeds 40,000, the low temperature fixability may be deteriorated.

The measurement of the molecular weight distribution by the gel permeation chromatography (GPC) can be performed, for example, as follows.
That is, first, the column is stabilized in a 40 ° C. heat chamber. At this temperature, tetrahydrofuran (THF) as a column solvent is allowed to flow at a flow rate of 1 ml per minute, and 50 to 200 μl of a tetrahydrofuran sample solution of a resin whose sample concentration is adjusted to 0.05 to 0.6 mass% is injected and measured. In measuring the molecular weight of the sample, the molecular weight distribution of the sample is calculated from the relationship between the logarithmic value of the calibration curve created by several monodisperse polystyrene standard samples and the count number. Examples of standard polystyrene samples for preparing the calibration curve include Pressure Chemical Co. Or Toyo Soda Kogyo Co., Ltd. having a molecular weight of ^{6 × 10 2, 2.1 × 10} 2, 4 × 10 2, 1.75 × 10 4, 1.1 × 10 5, 3.9 × 10 5, 8.6 It is preferable to use those of × 10 ⁵ , 2 × 10 ⁶ , and 4.48 × 10 ⁶ and use at least about 10 standard polystyrene samples. As the detector, an RI (refractive index) detector can be used.

-Other ingredients-
The other components are not particularly limited and may be appropriately selected depending on the purpose. For example, colorants, charge control agents, inorganic fine particles, fluidity improvers, cleaning improvers, magnetic materials, metal soaps , Etc.

The colorant is not particularly limited and may be appropriately selected from known dyes and pigments according to the purpose. For example, carbon black, nigrosine dye, iron black, naphthol yellow S, Hansa yellow (10G, 5G, G), cadmium yellow, yellow iron oxide, ocher, yellow lead, titanium yellow, polyazo yellow, oil yellow, Hansa yellow (GR, A, RN, R), pigment yellow L, benzidine yellow (G, GR), Permanent Yellow (NCG), Vulcan Fast Yellow (5G, R), Tartrazine Lake, Quinoline Yellow Lake, Anthrazan Yellow BGL, Isoindolinone Yellow, Bengala, Lead Red, Lead Red, Cadmium Red, Cad Muum Mercury Red, Antimon Zhu, Permanent Red 4R, PA Red, Faise Red, Parachlor Ortho Nitroaniline Red, Resol Fast Scarlet G, Brilliant Fast Scarlet, Brilliant Carmine BS, Permanent Red (F2R, F4R, FRL, FRLL, F4RH), Fast Scarlet VD, Belkan Fast Rubin B, Brilliant Scarlet G, Risor Rubin GX, Permanent Red F5R, Brilliant Carmine 6B, Pogment Scarlet 3B, Bordeaux 5B, Toluidine Maroon, Permanent Bordeaux F2K, Helio Bordeaux BL, Bordeaux 10B, Bon Maroon Light, Bon Maroon Medium, Eosin Lake, Rhodamine Lake B, Rhodamine Lake Y, Alizarin Lake, Thioindigo Red B, Thioindigo Maroon, Oh Lured, Quinacridone Red, Pyrazolone Red, Polyazo Red, Chrome Vermilion, Benzidine Orange, Perinone Orange, Oil Orange, Cobalt Blue, Cerulean Blue, Alkaline Blue Lake, Peacock Blue Lake, Victoria Blue Lake, Metal Free Phthalocyanine Blue, Phthalocyanine Blue, Fast Sky Blue, Indanthrene Blue (RS, BC), Indigo, Ultramarine Blue, Bitumen, Anthraquinone Blue, Fast Violet B, Methyl Violet Lake, Cobalt Purple, Manganese Purple, Dioxane Violet, Anthraquinone Violet, Chrome Green, Zinc Green, Oxidation Chrome, Pyridian, Emerald Green, Pigment Green B, Naphthol Green B, Green Gold, Ash Examples include green lake, malachite green lake, phthalocyanine green, anthraquinone green, titanium oxide, zinc white, and lithobon.
These may be used individually by 1 type and may use 2 or more types together.

The content of the colorant in the toner is not particularly limited and may be appropriately selected depending on the intended purpose, but is preferably 1 to 15% by mass, and more preferably 3 to 10% by mass.
When the content is less than 1% by mass, a reduction in the coloring power of the toner is observed. When the content exceeds 15% by mass, poor pigment dispersion in the toner occurs, the coloring power decreases, The characteristics may be degraded.

  The colorant may be used as a master batch combined with a resin. The resin is not particularly limited and may be appropriately selected from known ones according to the purpose. For example, styrene or a substituted polymer thereof, a styrene copolymer, polymethyl methacrylate, polybutyl methacrylate , Polyvinyl chloride, polyvinyl acetate, polyethylene, polypropylene, polyester, epoxy resin, epoxy polyol resin, polyurethane, polyamide, polyvinyl butyral, polyacrylic acid resin, rosin, modified rosin, terpene resin, aliphatic hydrocarbon resin, alicyclic ring Aromatic hydrocarbon resin, aromatic petroleum resin, chlorinated paraffin, paraffin, and the like. These may be used individually by 1 type and may use 2 or more types together.

  Examples of the polymer of styrene or a substituted product thereof include polyester resin, polystyrene, poly p-chlorostyrene, polyvinyl toluene, and the like. Examples of the styrene copolymer include a styrene-p-chlorostyrene copolymer, a styrene-propylene copolymer, a styrene-vinyltoluene copolymer, a styrene-vinylnaphthalene copolymer, and a styrene-methyl acrylate copolymer. Polymer, styrene-ethyl acrylate copolymer, styrene-butyl acrylate copolymer, styrene-octyl acrylate copolymer, styrene-methyl methacrylate copolymer, styrene-ethyl methacrylate copolymer, styrene- Butyl methacrylate copolymer, styrene-α-chloromethyl methacrylate copolymer, styrene-acrylonitrile copolymer, styrene-vinyl methyl ketone copolymer, styrene-butadiene copolymer, styrene-isoprene copolymer, styrene An acrylonitrile-indene copolymer, Styrene - maleic acid copolymer, styrene - maleic acid ester copolymer, and the like.

  The masterbatch can be produced by mixing or kneading the masterbatch resin and the colorant under high shear. At this time, it is preferable to add an organic solvent in order to enhance the interaction between the colorant and the resin. Also, the so-called flushing method is preferable in that the wet cake of the colorant can be used as it is, and there is no need to dry it. This flushing method is a method of mixing or kneading an aqueous paste containing water of a colorant together with a resin and an organic solvent, and transferring the colorant to the resin side to remove moisture and organic solvent components. For the mixing or kneading, for example, a high shear dispersion device such as a three-roll mill is preferably used.

The charge control agent is not particularly limited and may be appropriately selected from known materials according to the purpose. However, since a color tone may change when a colored material is used, a material that is colorless to nearly white is used. Preferably, for example, triphenylmethane dyes, molybdate chelate pigments, rhodamine dyes, alkoxyamines, quaternary ammonium salts (including fluorine-modified quaternary ammonium salts), alkylamides, phosphorus alone or compounds thereof, tungsten Examples thereof include a single substance or a compound thereof, a fluorine-based activator, a metal salt of salicylic acid, and a metal salt of a salicylic acid derivative. These may be used individually by 1 type and may use 2 or more types together.
Commercially available products may be used as the charge control agent. Examples of the commercially available products include quaternary ammonium salt Bontron P-51, oxynaphthoic acid metal complex E-82, and salicylic acid metal complex. E-84, phenolic condensate E-89 (above, manufactured by Orient Chemical Co., Ltd.), quaternary ammonium salt molybdenum complex TP-302, TP-415 (above, manufactured by Hodogaya Chemical Co., Ltd.), fourth Copy charge PSY VP2038 of quaternary ammonium salt, copy blue PR of triphenylmethane derivative, copy charge of quaternary ammonium salt NEG VP2036, copy charge NX VP434 (manufactured by Hoechst), LRA-901, LR which is a boron complex -147 (manufactured by Nippon Carlit), quinacridone, azo pigments, other sulfonic acid groups, carbo Sill group, polymer compounds having a functional group such as quaternary ammonium salts, and the like.
The charge control agent may be melted and kneaded together with the master batch and then dissolved or dispersed, or may be added together with the toner components when directly dissolving or dispersing in the organic solvent, or The toner particles may be fixed on the toner surface after production.

  The content of the charge control agent in the toner varies depending on the type of the binder resin, the presence / absence of an additive, a dispersion method, and the like, and cannot be generally specified. On the other hand, 0.1-10 mass parts is preferable, and 0.2-5 mass parts is more preferable. When the content is less than 0.1 parts by mass, the charge controllability may not be obtained. When the content exceeds 10 parts by mass, the chargeability of the toner becomes too large, and the effect of the main charge control agent is reduced. As a result, the electrostatic attractive force with the developing roller increases, which may lead to a decrease in developer fluidity and a decrease in image density.

The inorganic fine particles are not particularly limited and may be appropriately selected from known ones according to the purpose. For example, silica, alumina, titanium oxide, barium titanate, magnesium titanate, calcium titanate, titanate Strontium, zinc oxide, tin oxide, silica sand, clay, mica, wollastonite, diatomaceous earth, chromium oxide, cerium oxide, pengala, antimony trioxide, magnesium oxide, zirconium oxide, barium sulfate, barium carbonate, calcium carbonate, carbonized Examples include silicon and silicon nitride. These may be used individually by 1 type and may use 2 or more types together.
The primary particle diameter of the inorganic fine particles is preferably 5 nm to 2 μm, and more preferably 5 nm to 500 nm. The specific surface area of the inorganic fine particles by BET method is preferably 20 to 500 m ² / g.
The content of the inorganic fine particles in the toner is preferably 0.01 to 5.0% by mass, and more preferably 0.01 to 5.0% by mass.

The fluidity improver means a material that can be surface treated to increase hydrophobicity and prevent deterioration of flow characteristics and charging characteristics even under high humidity. For example, a silane coupling agent, a silylating agent, Examples thereof include a silane coupling agent having a fluoroalkyl group, an organic titanate coupling agent, an aluminum coupling agent, silicone oil, and modified silicone oil.
The cleaning improver is added to the toner in order to remove the developer after transfer remaining on the photoreceptor or the primary transfer medium. For example, a fatty acid metal salt such as zinc stearate, calcium stearate, stearic acid, Examples thereof include polymer fine particles produced by soap-free emulsion polymerization such as methyl methacrylate fine particles and polystyrene fine particles. The polymer fine particles preferably have a relatively narrow particle size distribution, and those having a volume average particle size of 0.01 to 1 μm are suitable.
There is no restriction | limiting in particular as said magnetic material, According to the objective, it can select suitably from well-known things, For example, iron powder, a magnetite, a ferrite, etc. are mentioned. Among these, white is preferable in terms of color tone.

-Aqueous medium-
The aqueous medium is not particularly limited and may be appropriately selected from known ones. Examples thereof include water, solvents miscible with water, and mixtures thereof. Among these, Is particularly preferred.
The solvent miscible with water is not particularly limited as long as it is miscible with water, and examples thereof include alcohol, dimethylformamide, tetrahydrofuran, cellosolves, and lower ketones.
Examples of the alcohol include methanol, isopropanol, ethylene glycol and the like. Examples of the lower ketones include acetone and methyl ethyl ketone.
These may be used individually by 1 type and may use 2 or more types together.
In the toner manufacturing method according to the first aspect of the present invention, as described above, it is necessary that the aqueous medium does not contain organic resin fine particles.

-Dispersed particles-
The dispersed particles are dispersions (oil droplets) formed by dissolving or dispersing the toner material in the aqueous medium and formed by dispersing or dissolving the toner material in the aqueous medium, and the composition of the dispersed particles Is the same as the composition of the solution or dispersion of the toner material. That is, the dispersed particles include, for example, at least one of the monomer, the polymer, and a polymer (prepolymer) that can react with the active hydrogen group-containing compound, and if necessary, the colorant, And a toner material containing the other components such as the charge control agent.
The dispersion particles are formed by preparing an oil-in-water dispersion by dispersing the toner material in the aqueous medium.

  The volume average particle diameter (Mv) of the dispersed particles is not particularly limited and may be appropriately selected depending on the intended purpose. However, the method for producing the toner of the first and fourth aspects of the present invention is not limited. In the toner, the volume average particle size before granulating the toner is preferably 0.1 to 3 μm, more preferably 0.1 to 2 μm, and still more preferably 0.1 to 1 μm. In the method for producing the toner according to the second aspect and the third aspect of the present invention, the volume average particle diameter (Mv) before increasing the volume average particle diameter, that is, when preparing the oil-in-water dispersion. However, it is necessary that it is 0.1-3 micrometers, 0.1-2 micrometers is preferable and 0.1-1 micrometer is more preferable. When the volume average particle size (Mv) of the dispersed particles is very small, there is no bias in the composition of the material between the toner particles formed by combining the dispersed particles, and the charge amount is uniform among the particles. Therefore, a toner having excellent chargeability is granulated.

  The dissolution or dispersion of the toner material in the aqueous medium is preferably performed by dispersing the dissolution or dispersion of the toner material in the aqueous medium while stirring. The dispersion method is not particularly limited and can be appropriately selected according to the purpose. For example, the dispersion can be performed using a known disperser. Examples of the disperser include a low-speed shearing disperser. Machine, high-speed shearing disperser, friction disperser, high-pressure jet disperser, ultrasonic disperser, and the like. Among these, a high-speed shearing disperser is preferable in that the particle diameter of the dispersed particles can be controlled to 0.1 to 3 μm.

<Toner granulation process>
The toner granulating step is a step of granulating the toner by adding at least a water dispersion of wax to the oil-in-water dispersion and adding organic resin fine particles as necessary.
By adding a water dispersion of wax after the oil-in-water type dispersion preparation step (after formation of the dispersion particles), the wax particles are uniformly dispersed in the toner without using a dispersant, Further, it can be appropriately present on the toner surface, prevents the wax from being unevenly distributed in the toner particles, is excellent in releasability, chargeability, and the like, and can suppress the occurrence of filming on the photoreceptor.

-Aqueous dispersion of wax-
The wax aqueous dispersion is obtained by dispersing the wax in the aqueous medium.
The volume average particle diameter of the wax dispersion particles in the aqueous dispersion of wax is not particularly limited and may be appropriately selected depending on the intended purpose. 2 μm is preferable, and 0.1 to 1 μm is more preferable. If the volume average particle size of the dispersed particles of the wax is less than 0.1 μm, sufficient release performance may not be obtained, and if it exceeds 2 μm, the uniform dispersibility of the wax in the toner may deteriorate. is there.
The melting point of the wax is not particularly limited and may be appropriately selected depending on the intended purpose, but is preferably a low melting point from the viewpoint of improving low-temperature fixability, for example, 50 to 90 ° C. is preferable. 60 to 85 ° C is more preferable.
If the melting point is less than 50 ° C., the wax may adversely affect the heat resistant storage stability, and if it exceeds 90 ° C., a cold offset may easily occur during fixing at a low temperature.

The wax is not particularly limited as long as it can be dispersed in the aqueous medium, and can be appropriately selected according to the purpose. Examples thereof include long-chain hydrocarbons, carbonyl group-containing waxes, and polyolefin waxes. These may be used individually by 1 type and may use 2 or more types together. Of these, long chain hydrocarbons are preferred.
Examples of the long chain hydrocarbon include paraffin wax and sazol wax. Among these, paraffin wax having a low melting point is preferable from the viewpoint of improving low-temperature fixability.
Examples of the carbonyl group-containing wax include polyalkanoic acid esters, polyalkanol esters, polyalkanoic acid amides, polyalkylamides, dialkyl ketones, and the like. Examples of the polyalkanoic acid ester include carnauba wax, montan wax, trimethylolpropane tribehenate, pentaerythritol tetrabehenate, pentaerythritol diacetate dibehenate, glycerin tribehenate, and 1,18-octadecane. Examples thereof include diol distearate. Examples of the polyalkanol ester include tristearyl trimellitic acid and distearyl maleate. Examples of the polyalkanoic acid amide include dibehenyl amide. Examples of the polyalkylamide include trimellitic acid tristearylamide. Examples of the dialkyl ketone include distearyl ketone. Among these carbonyl group-containing waxes, polyalkanoic acid esters are particularly preferable.
Examples of the polyolefin wax include polyethylene wax and polypropylene wax.

  As described above, the wax needs to be added as an aqueous dispersion. However, the wax is added to the solution or dispersion of the toner material, and the wax is dispersed in the solution or dispersion. You may use together. By including a plurality of types of the wax in the toner, one toner can be provided with multiple functions.

There is no restriction | limiting in particular as content in the said toner of the said wax, Although it can select suitably according to the objective, 0-40 mass% is preferable and 3-30 mass% is more preferable.
When the content exceeds 40% by mass, the fluidity of the toner may be deteriorated.

-Organic resin fine particles-
In the first toner production method of the present invention, after the oil-in-water type dispersion preparation step, in the toner granulation step, the organic resin fine particles are added, and the toner is produced in the presence of the organic resin fine particles. It is necessary to granulate. As described above, in the oil-in-water dispersion preparation step, fine dispersion particles can be obtained by not including the organic resin fine particles in the aqueous medium, and the organic resin is used in the toner granulation step. By adding fine particles, the shape and particle size distribution of the toner can be controlled, and a toner having a narrow particle size distribution can be obtained.
The organic resin fine particles can change the particle size of the toner depending on the addition amount thereof, and the addition amount of the organic resin fine particles to the oil-in-water dispersion is not particularly limited, depending on the purpose. It can select suitably, For example, 0.5-10 mass% is preferable.

The organic resin fine particle is not particularly limited as long as it is a resin that can form an aqueous dispersion in the oil-in-water dispersion, and can be appropriately selected from known resins according to the purpose. It may be a plastic resin or a thermosetting resin. For example, vinyl resin, polyurethane resin, epoxy resin, polyester resin, polyamide resin, polyimide resin, silicon resin, phenol resin, melamine resin, urea resin, aniline resin , Ionomer resin, polycarbonate resin, and the like.
These may be used individually by 1 type and may use 2 or more types together. Among these, at least one selected from vinyl resins, polyurethane resins, epoxy resins, and polyester resins is preferable because an aqueous dispersion of fine spherical resin particles can be easily obtained.
The vinyl resin is a polymer obtained by homopolymerizing or copolymerizing a vinyl monomer. For example, a styrene- (meth) acrylic acid ester resin, a styrene-butadiene copolymer, a (meth) acrylic acid-acrylic acid ester polymer. Styrene-acrylonitrile copolymer, styrene-maleic anhydride copolymer, styrene- (meth) acrylic acid copolymer, and the like.
Further, as the organic resin fine particles, a copolymer comprising a monomer having at least two unsaturated groups can be used.
The monomer having at least two unsaturated groups is not particularly limited and may be appropriately selected depending on the intended purpose. For example, a sodium salt of ethylene oxide methacrylate adduct sulfate (“Eleminol RS-30”). "; Manufactured by Sanyo Chemical Industries Ltd.), divinylbenzene, 1,6-hexanediol acrylate and the like.

  The organic resin fine particles can be obtained by polymerization according to a known method appropriately selected according to the purpose, but is preferably obtained as an aqueous dispersion of the organic resin fine particles. As the method for preparing the aqueous dispersion of the organic resin fine particles, for example, (1) In the case of the vinyl resin, a vinyl monomer is used as a starting material and selected from suspension polymerization, emulsion polymerization, seed polymerization, and dispersion polymerization (2) In the case of polyaddition or condensation resin such as polyester resin, polyurethane resin and epoxy resin, a precursor (monomer). , Oligomers, etc.) or a solvent solution thereof in the presence of a suitable dispersant, and then dispersed in an aqueous medium, followed by heating or adding a curing agent and curing to produce an aqueous dispersion of organic resin fine particles (3) In the case of polyaddition or condensation resin such as polyester resin, polyurethane resin, epoxy resin, etc., precursor (monomer, oligomer, etc.) or solvent solution (liquid) (It may be liquefied by heating) After dissolving an appropriate emulsifier in water, water is added and phase inversion emulsification is performed. (4) Polymerization reaction (addition polymerization, ring-opening polymerization, polyaddition) in advance The resin prepared by any polymerization reaction mode such as addition condensation, condensation polymerization, etc.) is pulverized using a mechanical rotating type or jet type fine pulverizer, and then classified to give organic resin fine particles. (5) A polymerization reaction (addition polymerization, ring-opening polymerization, polyaddition, addition condensation, condensation polymerization or any other polymerization reaction mode) may be used in advance in the presence of an appropriate dispersant. (6) A method in which organic resin fine particles are obtained by spraying a resin solution prepared by dissolving a resin prepared in (1) in a solvent in the form of a mist, and then dispersing the organic resin fine particles in water in the presence of an appropriate dispersant. Polymerization reaction (addition polymerization, A resin prepared by dissolving a resin prepared by ring polymerization, polyaddition, addition condensation, condensation polymerization, or the like in a solvent, or a resin previously dissolved in a solvent by heating. (7) a method of precipitating organic resin fine particles by cooling the solution, then removing the solvent to obtain organic resin fine particles, and then dispersing the organic resin fine particles in water in the presence of a suitable dispersant; In the presence of a suitable dispersant, a resin solution prepared by dissolving a resin prepared by a polymerization reaction (any polymerization reaction mode such as addition polymerization, ring-opening polymerization, polyaddition, addition condensation, condensation polymerization, etc.) in a solvent, (8) A polymerization reaction (addition polymerization, ring-opening polymerization, polyaddition, addition condensation, condensation polymerization or any other polymerization reaction mode) is performed in advance by dispersing the solvent in an aqueous medium and then removing the solvent by heating or decompression. May) A preferable method includes, for example, a method in which a suitable emulsifier is dissolved in a resin solution obtained by dissolving the prepared resin in a solvent and then water is added to perform phase inversion emulsification.

When adding the organic resin fine particles, it is preferable to add an ionizing agent together with the organic resin fine particles. By adding the ionizing agent, the dispersed particles can be united, and the dispersed particles can be grown to a desired particle size.
The ionizing agent is not particularly limited as long as the dispersed particles can be agglomerated, and can be appropriately selected according to the purpose, but is selected from a salt composed of a monovalent cation and a monovalent anion. It is preferable that it is at least one kind.
There is no restriction | limiting in particular as said monovalent cation in the salt which consists of said monovalent cation and a monovalent anion, Although it can select suitably according to the objective, For example, sodium ion, potassium Ions and the like are preferable.
Therefore, specific examples of the ionizing agent include sodium chloride, potassium chloride, sodium hydroxide, potassium hydroxide, and the like.
Further, when the aqueous dispersion of wax and the organic resin fine particles are added to the oil-in-water dispersion, the addition is performed after the oil-in-water dispersion preparation step, the aqueous dispersion of wax, the organic It is preferable to carry out in the order of resin fine particles.

  In the toner granulation step, in the toner production method according to the second aspect, the third aspect, and the fourth aspect of the present invention, the volume average particle diameter of the dispersed particles after being increased is as follows: It is necessary to be larger than the volume average particle diameter of the dispersed particles before increasing. By granulating the toner after increasing the fine dispersed particles formed in the oil-in-water type dispersion preparation step, the composition of the material between the toner particles is uniform, and the chargeability, fixability, etc. An excellent toner having a small particle size and a narrow particle size distribution can be obtained.

In the method for producing the toner of the second aspect and the third aspect of the present invention, the volume average particle size (Mv) of the dispersed particles obtained by the oil-in-water type dispersion preparation step is increased to 3 to 9 μm. Then, it is necessary to granulate the toner, and it is preferable to increase the toner to approximately the same size as the toner particles.
In the method for producing a toner according to the fourth aspect of the present invention, the volume average particle size (Mv) of the dispersed particles obtained by the oil-in-water type dispersion preparation step is increased by 3 to 45 times. It is necessary to granulate the toner, and it is preferable to increase it 3 to 30 times. The volume average particle size (Mv) is preferably increased within the range of the magnification (3 to 45 times) and 3 to 9 μm.
If the volume average particle size (Mv) is less than 3 times, the uniformity of the composition of the material in the toner particles may deteriorate, and if it exceeds 45 times, it becomes difficult to granulate the toner. The particle size distribution may be deteriorated and image degradation may occur.
In addition, it is preferable to add the ionizing agent when increasing the volume average particle diameter of the dispersed particles.

  In the oil-in-water type dispersion preparation step, the stirring speed when dissolving or dispersing the toner material in the aqueous medium is Am / s, and the stirring speed when granulating the toner is Bm / s. When s is satisfied, it is preferable to satisfy the following expressions: 7 <A <23 and 1.4 <A / B <100. When the stirring speed A at the time of dispersion satisfies the above formula, dispersed particles having a desired fine particle diameter can be obtained, and A / B is expressed in relation to the stirring speed B at the time of granulating the toner. When the above mathematical formula is satisfied, the particle size of the dispersed particles can be controlled and increased to a desired particle size, the composition of the material between the toner particles is uniform, excellent in charging property, fixing property, etc. A toner having a narrow particle size and a narrow particle size distribution can be obtained. That is, when the toner material is dissolved or dispersed in the aqueous medium, the dispersed particles can be formed by setting the stirring speed fast, and before granulating the toner, By setting the stirring speed slower than that at the time of dispersion, the dispersed particles can be united to increase the volume average particle diameter of the dispersed particles.

  In the method for producing a toner according to the preferred embodiment of the present invention, the active hydrogen group-containing compound and the active hydrogen group-containing compound can be reacted in the preparation step of the oil-in-water dispersion or the toner granulation step. Are subjected to an extension reaction or a cross-linking reaction to produce an adhesive substrate.

-Adhesive substrate-
The adhesive base material exhibits adhesiveness to a recording medium such as paper, and is formed by reacting the active hydrogen group-containing compound and a polymer capable of reacting with the active hydrogen group-containing compound in the aqueous medium. It may contain at least a polymer and may further contain a binder resin appropriately selected from known binder resins.

There is no restriction | limiting in particular as a weight average molecular weight of the said adhesive base material, Although it can select suitably according to the objective, For example, 3,000 or more are preferable and 5,000-1,000,000 are more preferable. 7,000 to 500,000 are particularly preferred.
When the weight average molecular weight is less than 3,000, the hot offset resistance may be deteriorated.

There is no restriction | limiting in particular as glass transition temperature (Tg) of the said adhesive base material, Although it can select suitably according to the objective, For example, 30-70 degreeC is preferable and 40-65 degreeC is more preferable. In the toner, since a polyester resin subjected to a crosslinking reaction and an extension reaction coexists, the toner exhibits good storage stability even when the glass transition temperature is lower than that of a conventional polyester toner.
When the glass transition temperature (Tg) is less than 30 ° C., the heat-resistant storage stability of the toner may deteriorate, and when it exceeds 70 ° C., the low-temperature fixability may not be sufficient.

  The glass transition temperature can be measured by, for example, the following method using a TG-DSC system TAS-100 (manufactured by Rigaku Corporation). First, about 10 mg of toner is placed in an aluminum sample container, and the sample container is placed on a holder unit and set in an electric furnace. After heating from room temperature to 150 ° C. at a rate of temperature increase of 10 ° C./min, the sample is left at 150 ° C. for 10 minutes, and the sample is cooled to room temperature and left for 10 minutes. Then, the DSC curve is measured with a differential scanning calorimeter (DSC) after heating to 150 ° C. at a temperature rising rate of 10 ° C./min in a nitrogen atmosphere. From the obtained DSC curve, using the analysis system in the TG-DSC system TAS-100 system, the glass transition temperature (Tg) is calculated from the contact point between the tangent line of the endothermic curve near the glass transition temperature (Tg) and the baseline. can do.

Specific examples of the adhesive substrate are not particularly limited and may be appropriately selected depending on the intended purpose. Particularly preferred are polyester resins.
There is no restriction | limiting in particular as said polyester-type resin, Although it can select suitably according to the objective, For example, a urea modified polyester-type resin etc. are mentioned especially suitably.
The urea-modified polyester resin comprises an amine (B) as the active hydrogen group-containing compound and an isocyanate group-containing polyester prepolymer (A) as a polymer that can react with the active hydrogen group-containing compound. Obtained by reacting in phase.
The urea-modified polyester resin may contain a urethane bond in addition to the urea bond. In this case, the molar ratio of the urea bond to the urethane bond (urea bond / urethane bond) is particularly limited. However, 100/0 to 10/90 is preferable, 80/20 to 20/80 is more preferable, and 60/40 to 30/70 is particularly preferable.
When the urea bond is less than 10, the hot offset resistance may be deteriorated.

  Preferable specific examples of the urea-modified polyester resin include the following (1) to (10), that is, (1) a polyester pre-reacted polycondensate of bisphenol A ethylene oxide 2 mol adduct and isophthalic acid with isophorone diisocyanate. A mixture of a polymer urealated with isophoronediamine and a polycondensate of bisphenol A ethylene oxide 2 mol adduct and isophthalic acid, (2) a polycondensate of bisphenol A ethylene oxide 2 mol adduct and isophthalic acid A mixture of a polyester prepolymer reacted with diisocyanate and uread with isophoronediamine, a bicondensate of bisphenol A ethylene oxide 2 mol adduct and terephthalic acid, (3) bisphenol A ethylene oxide 2 mol Polyester prepolymer obtained by reacting an adduct / bisphenol A propylene oxide 2 mol adduct and terephthalic acid polycondensate with isophorone diisocyanate and urethanized with isophorone diamine, and bisphenol A ethylene oxide 2 mol adduct / bisphenol A propylene Mixture of oxide 2 mol adduct and terephthalic acid polycondensate, (4) Bisphenol A ethylene oxide 2 mol adduct / bisphenol A propylene oxide 2 mol adduct and terephthalic acid polycondensate were reacted with isophorone diisocyanate. A mixture of a polyester prepolymer uread with isophoronediamine, a bisphenol A propylene oxide 2-mole adduct and a polycondensate of terephthalic acid, (5) bisphenol A Polyester prepolymer obtained by reacting a polycondensate of tylene oxide 2 mol adduct and terephthalic acid with isophorone diisocyanate and ureaated with hexamethylenediamine, a polycondensate of bisphenol A ethylene oxide 2 mol adduct and terephthalic acid (6) Polyester prepolymer obtained by reacting polycondensate of bisphenol A ethylene oxide with 2 mol of bisphenol A and isophorone diisocyanate with urea and hexamethylenediamine and 2 mol of bisphenol A ethylene oxide. Product / bisphenol A propylene oxide 2 mol adduct and terephthalic acid polycondensate, (7) bisphenol A ethylene oxide 2 mol adduct and terephthalic acid polycondensate A mixture of a polyester prepolymer reacted with socyanate with urethanized with ethylenediamine and a polycondensate of bisphenol A ethylene oxide 2 mol adduct and terephthalic acid, (8) bisphenol A ethylene oxide 2 mol adduct and isophthalic acid A mixture of a polyester prepolymer obtained by reacting a polycondensate of bisphenol with diphenylmethane diisocyanate with urea and hexamethylenediamine, and a polycondensate of bisphenol A ethylene oxide 2 mol adduct and isophthalic acid, (9) bisphenol A ethylene Polyester prepolymer obtained by reacting polycondensate of oxide 2 mol adduct / bisphenol A propylene oxide 2 mol adduct and terephthalic acid / dodecenyl succinic anhydride with diphenylmethane diisocyanate Mixture of uremer urea-modified with hexamethylenediamine and bisphenol A ethylene oxide 2-mole adduct / bisphenol A propylene oxide 2-mole adduct and terephthalic acid polycondensate, (10) bisphenol A ethylene oxide 2-mole addition And a mixture of a polyester prepolymer obtained by reacting a polycondensate of isophthalic acid and isophthalic acid with toluene diisocyanate with urea methylenediamine, a 2-mole adduct of bisphenol A ethylene oxide and a polycondensate of isophthalic acid, etc. Preferably mentioned.

--Binder resin--
There is no restriction | limiting in particular as said binder resin, According to the objective, it can select suitably, For example, although a polyester resin etc. are mentioned, Undenatured polyester resin (unmodified polyester resin) is especially preferable.
When the unmodified polyester resin is contained in the toner, low-temperature fixability and glossiness can be improved.
Examples of the unmodified polyester resin include those similar to the urea bond-forming group-containing polyester resin, that is, a polycondensate of a polyol (PO) and a polycarboxylic acid (PC). The unmodified polyester resin is partially compatible with the urea bond-forming group-containing polyester resin (RMPE), that is, has a similar structure that is compatible with each other. It is preferable in terms of resistance to hot offset.

The weight average molecular weight (Mw) of the unmodified polyester resin is preferably 1,000 to 30,000, preferably 1,500 to 15, in terms of molecular weight distribution by GPC (gel permeation chromatography) soluble in tetrahydrofuran (THF). 1,000 is more preferred. When the weight average molecular weight (Mw) is less than 1,000, the heat resistant storage stability may be deteriorated. Therefore, as described above, the content of the component having the weight average molecular weight (Mw) of less than 1,000. Is required to be 8 to 28% by mass. On the other hand, when the weight average molecular weight (Mw) exceeds 30,000, the low-temperature fixability may be deteriorated.
The glass transition temperature of the unmodified polyester resin is preferably 35 to 70 ° C. When the glass transition temperature is less than 35 ° C., the heat-resistant storage stability of the toner may be deteriorated, and when it exceeds 70 ° C., the low-temperature fixability may be insufficient.
The hydroxyl value of the unmodified polyester resin is preferably 5 mgKOH / g, more preferably 10 to 120 mgKOH / g, and still more preferably 20 to 80 mgKOH / g. If the hydroxyl value is less than 5, it may be difficult to achieve both heat-resistant storage stability and low-temperature fixability.
The acid value of the unmodified polyester resin is usually 1.0 to 30.0 mgKOH / g, and preferably 5.0 to 20.0 mgKOH / g. Generally, it becomes easy to be negatively charged by giving the toner an acid value.
When the unmodified polyester resin is contained in the toner, the mixing mass ratio (RMPE / PE) of the urea bond-forming group-containing polyester resin (RMPE) and the unmodified polyester resin (PE) is 5/95. -25/75 is preferable, and 10 / 90-25 / 75 is more preferable.
When the mixing mass ratio of the unmodified polyester resin (PE) exceeds 95, the hot offset resistance may be deteriorated. .

  The adhesive substrate (for example, the urea-modified polyester resin) includes, for example, (1) a polymer that can react with the active hydrogen group-containing compound (for example, the isocyanate group-containing polyester prepolymer (A)). A solution or dispersion of the toner material is emulsified or dispersed in the aqueous medium together with the active hydrogen group-containing compound (for example, the amines (B)) to form the dispersed particles, and both in the aqueous medium. (2) The dispersion or dispersion of the toner material is emulsified or dispersed in the aqueous medium to which the active hydrogen group-containing compound has been added in advance, and the dispersion is performed. It may be formed by forming particles and subjecting both to an extension reaction or a crosslinking reaction in the aqueous medium, or (3) a solution or dispersion of the toner material. After adding and mixing in the aqueous medium, the active hydrogen group-containing compound is added to form the dispersed particles, and these are formed by extending or cross-linking both from the particle interface in the aqueous medium. May be. In the case of (3), a modified polyester resin is preferentially produced on the surface of the toner to be produced, and a concentration gradient can be provided in the toner particles.

  The reaction conditions for producing the adhesive base material by the emulsification or dispersion are not particularly limited, depending on the combination of the polymer capable of reacting with the active hydrogen group-containing compound and the active hydrogen group-containing compound. The reaction time is preferably 10 minutes to 40 hours, more preferably 2 hours to 24 hours, and the reaction temperature is preferably 0 to 150 ° C, more preferably 40 to 98 ° C.

  Examples of a method for stably forming the dispersed particles containing a polymer capable of reacting with the active hydrogen group-containing compound (for example, the isocyanate group-containing polyester prepolymer (A)) in the aqueous medium include, for example, the aqueous system. In the medium, the toner material such as a polymer capable of reacting with the active hydrogen group-containing compound (for example, the isocyanate group-containing polyester prepolymer (A)), the colorant, the charge control agent, and the unmodified polyester resin. And a method of adding a solution or dispersion liquid of the toner material prepared by dissolving or dispersing the toner material in the organic solvent and dispersing the toner material by a shearing force.

In the emulsification or dispersion, the amount of the aqueous medium used is preferably 50 to 2,000 parts by mass, more preferably 100 to 1,000 parts by mass with respect to 100 parts by mass of the toner material.
If the amount used is less than 50 parts by mass, the toner material may be poorly dispersed and toner particles having a predetermined particle size may not be obtained. If the amount used exceeds 2,000 parts by mass, the production cost will be high. May be.

In the emulsification or dispersion, a dispersant is preferably used from the viewpoint of stabilizing the dispersed particles and sharpening the particle size distribution while obtaining a desired shape, if necessary.
There is no restriction | limiting in particular as said dispersing agent, According to the objective, it can select suitably, For example, surfactant, a sparingly water-soluble inorganic compound dispersing agent, a polymeric protective colloid, etc. are mentioned. These may be used individually by 1 type and may use 2 or more types together. Among these, surfactants are preferable.

Examples of the surfactant include an anionic surfactant, a cationic surfactant, a nonionic surfactant, and an amphoteric surfactant.
Examples of the anionic surfactant include alkylbenzene sulfonates, α-olefin sulfonates, phosphate esters and the like, and those having a fluoroalkyl group are preferable. Examples of the anionic surfactant having a fluoroalkyl group include a fluoroalkylcarboxylic acid having 2 to 10 carbon atoms or a metal salt thereof, disodium perfluorooctanesulfonylglutamate, 3- [omega-fluoroalkyl (6 carbon atoms). -11) Oxy] -1-alkyl (carbon number 3-4) sodium sulfonate, 3- [omega-fluoroalkanoyl (carbon number 6-8) -N-ethylamino] -1-propanesulfonic acid sodium, fluoroalkyl (Carbon number 11-20) carboxylic acid or its metal salt, perfluoroalkyl carboxylic acid (carbon number 7-13) or its metal salt, perfluoroalkyl (carbon number 4-12) sulfonic acid or its metal salt, perfluoro Octanesulfonic acid diethanolamide, N-propyl-N- (2-hydroxy Ethyl) perfluorooctanesulfonamide, perfluoroalkyl (carbon number 6-10) sulfonamidopropyltrimethylammonium salt, perfluoroalkyl (carbon number 6-10) -N-ethylsulfonylglycine salt, monoperfluoroalkyl (carbon number) 6-16) Ethyl phosphate and the like. Examples of commercially available surfactants having a fluoroalkyl group include Surflon S-111, S-112, S-113 (manufactured by Asahi Glass Co., Ltd.); Fluorard FC-93, FC-95, FC-98, FC- 129 (manufactured by Sumitomo 3M); Unidyne DS-101, DS-102 (manufactured by Daikin Industries); Megafac F-110, F-120, F-113, F-191, F-812, F-833 (large) Nihon Ink Co., Ltd.); Xtop EF-102, 103, 104, 105, 112, 123A, 123B, 306A, 501, 201, 204 (manufactured by Tochem Products); Manufactured) and the like.

  Examples of the cationic surfactant include amine salt type surfactants and quaternary ammonium salt type cationic surfactants. Examples of the amine salt type surfactant include alkylamine salts, amino alcohol fatty acid derivatives, polyamine fatty acid derivatives, imidazolines, and the like. Examples of the quaternary ammonium salt type cationic surfactant include alkyltrimethylammonium salt, dialkyldimethylammonium salt, alkyldimethylbenzylammonium salt, pyridinium salt, alkylisoquinolinium salt, benzethonium chloride and the like. . Among the cationic surfactants, aliphatic quaternary ammonium such as aliphatic primary, secondary or tertiary amine acids having a fluoroalkyl group, perfluoroalkyl (6 to 10 carbon atoms) sulfonamidopropyltrimethylammonium salt, etc. Salts, benzalkonium salts, benzethonium chloride, pyridinium salts, imidazolinium salts, and the like. Commercially available products of the cationic surfactant include, for example, Surflon S-121 (manufactured by Asahi Glass Co., Ltd.); Florard FC-135 (manufactured by Sumitomo 3M Co.); Unidyne DS-202 (manufactured by Daikin Industries Ltd.), MegaFuck F-150 F-824 (manufactured by Dainippon Ink Co., Ltd.); Xtop EF-132 (manufactured by Tochem Products); Footgent F-300 (manufactured by Neos).

Examples of the nonionic surfactant include fatty acid amide derivatives and polyhydric alcohol derivatives.
Examples of the amphoteric surfactant include alanine, dodecyldi (aminoethyl) glycine, di (octylaminoethyl) glycine, N-alkyl-N, N-dimethylammonium betaine, and the like.

Examples of the poorly water-soluble inorganic compound dispersant include tricalcium phosphate, calcium carbonate, titanium oxide, colloidal silica, and hydroxyapatite.
Examples of the polymeric protective colloid include acids, (meth) acrylic monomers containing hydroxyl groups, vinyl alcohol or ethers of vinyl alcohol, esters of vinyl alcohol and compounds containing carboxyl groups, amides Examples thereof include homopolymers or copolymers of compounds or their methylol compounds, chlorides, those having a nitrogen atom or a heterocyclic ring thereof, polyoxyethylenes, celluloses, and the like.
Examples of the acids include acrylic acid, methacrylic acid, α-cyanoacrylic acid, α-cyanomethacrylic acid, itaconic acid, crotonic acid, fumaric acid, maleic acid, maleic anhydride, and the like. Examples of the (meth) acrylic monomer containing a hydroxyl group include β-hydroxyethyl acrylate, β-hydroxyethyl methacrylate, β-hydroxypropyl acrylate, β-hydroxypropyl methacrylate, and γ-acrylate. -Hydroxypropyl, γ-hydroxypropyl methacrylate, 3-chloro-2-hydroxypropyl acrylate, 3-chloro-2-hydroxypropyl methacrylate, diethylene glycol monoacrylate, diethylene glycol monomethacrylate, glycerol monoacrylate Glycerin monomethacrylic acid ester, N-methylol acrylamide, N-methylol methacrylamide and the like. Examples of the vinyl alcohol or ethers with vinyl alcohol include vinyl methyl ether, vinyl ethyl ether, vinyl propyl ether, and the like. Examples of the esters of vinyl alcohol and a compound containing a carboxyl group include vinyl acetate, vinyl propionate, and vinyl butyrate. Examples of the amide compound or these methylol compounds include acrylamide, methacrylamide, diacetone acrylamide acid, or these methylol compounds. Examples of the chlorides include acrylic acid chloride and methacrylic acid chloride. Examples of the homopolymer or copolymer such as those having a nitrogen atom or a heterocyclic ring thereof include vinyl pyridine, vinyl pyrrolidone, vinyl imidazole, and ethylene imine. Examples of the polyoxyethylene are polyoxyethylene, polyoxypropylene, polyoxyethylene alkylamine, polyoxypropylene alkylamine, polyoxyethylene alkylamide, polyoxypropylene alkylamide, polyoxyethylene nonylphenyl ether, polyoxyethylene Examples thereof include oxyethylene lauryl phenyl ether, polyoxyethylene stearyl phenyl ester, and polyoxyethylene nonyl phenyl ester. Examples of the celluloses include methyl cellulose, hydroxyethyl cellulose, and hydroxypropyl cellulose.

In the preparation of the oil-in-water dispersion, a dispersion stabilizer can be used as necessary.
Examples of the dispersion stabilizer include acids that are soluble in acids and alkalis such as calcium phosphate.
When the dispersion stabilizer is used, the calcium phosphate salt can be removed from the fine particles by a method of dissolving the calcium phosphate salt with an acid such as hydrochloric acid and then washing with water or a method of decomposing with an enzyme.

  In the preparation of the oil-in-water dispersion, the catalyst for the extension reaction or the crosslinking reaction can be used. Examples of the catalyst include dibutyltin laurate and dioctyltin laurate.

In the toner granulation step, the dispersed particles formed in the oil-in-water dispersion preparation step are combined, and then the organic solvent is removed from the dispersed particles.
The organic solvent is removed, for example, when the toner is produced by a known dissolution suspension method or the toner production method of the preferred embodiment of the present invention.

The removal of the organic solvent includes (1) a method in which the entire reaction system is gradually decompressed to completely evaporate and remove the organic solvent in the dispersed particles, and (2) the entire reaction system is gradually heated. A method of completely evaporating and removing the organic solvent in the dispersed particles, and (3) spraying an oil-in-water dispersion in a dry atmosphere to completely remove the water-insoluble organic solvent in the dispersed particles. Examples thereof include a method of forming toner fine particles and evaporating and removing the aqueous dispersant together.
The dry atmosphere in which the oil-in-water dispersion is sprayed includes, for example, heated gas such as air, nitrogen, carbon dioxide, combustion gas, and various air currents heated to a temperature higher than the boiling point of the highest boiling solvent used. Etc. These can sufficiently achieve the intended quality by short-time treatment using a spray dryer, belt dryer, rotary dryer, rotary kiln or the like.

  When the organic solvent is removed, toner particles are formed. The toner particles can be washed, dried, etc., and then classified as desired. The classification can be performed, for example, by removing fine particle portions by a cyclone, a decanter, centrifugation, or the like in a liquid, and the classification operation may be performed after obtaining a powder after drying.

The toner particles thus obtained are mixed with the particles of the colorant, the wax, the charge control agent and the like, and further, a mechanical impact force is applied to the particles of the wax from the surface of the toner particles. Can be prevented from desorbing.
As the method for applying the mechanical impact force, for example, a method in which an impact force is applied to the mixture by blades rotating at a high speed, a mixture is introduced into a high-speed air stream and accelerated to appropriately collide particles or composite particles. The method of making it collide with a board, etc. are mentioned. As an apparatus used for this method, for example, an ong mill (manufactured by Hosokawa Micron Co., Ltd.), an I-type mill (manufactured by Nippon Pneumatic Co., Ltd.) and a pulverization air pressure is lowered, and a hybridization system (Nara Machinery Co., Ltd.) Product), kryptron system (manufactured by Kawasaki Heavy Industries, Ltd.), automatic mortar, and the like.

  The toner obtained by the toner production method of the present invention has the following volume average particle diameter (Dv), volume average particle diameter (Dv) / number average particle diameter (Dn), penetration, low temperature fixability, It preferably has an offset non-occurrence temperature, thermal characteristics, glass transition temperature, acid value, image density, and the like.

The volume average particle diameter (Dv) of the toner is preferably 3 to 9 μm, and more preferably 3 to 7 μm, for example.
When the volume average particle size is less than 3 μm, in the two-component developer, the toner may be fused to the surface of the carrier during a long period of stirring in the developing device, and the charging ability of the carrier may be reduced. In a developer, toner filming on the developing roller and toner fusion to a member such as a blade are likely to occur because the toner is thinned. When the thickness exceeds 9 μm, the resolution is high and high. It becomes difficult to obtain an image of an image quality, and when the balance of the toner in the developer is performed, the variation in the particle diameter of the toner may increase.

The ratio (Dv / Dn) of the volume average particle diameter (Dv) to the number average particle diameter (Dn) in the toner is, for example, preferably 1.05 to 1.25, more preferably 1.05 to 1.20. preferable.
When the ratio of the volume average particle diameter to the number average particle diameter (Dv / Dn) is less than 1.05, in the two-component developer, the toner is fused to the surface of the carrier during long-term stirring in the developing device, The chargeability of the carrier may be reduced, and the cleaning property may be deteriorated. In the case of a one-component developer, the filming of the toner on the developing roller and the thinning of the toner are performed. Toner fusion may easily occur, and if it exceeds 1.25, it becomes difficult to obtain a high-resolution and high-quality image, and toner particles in the case where the balance of the toner in the developer is performed Variation in diameter may be large.
When the ratio of the volume average particle diameter to the number average particle diameter (Dv / Dn) is 1.05 to 1.20, the heat resistant storage stability, the low temperature fixability, and the hot offset resistance are all excellent. In particular, when used in a full-color copying machine, the glossiness of the image is excellent. With two-component developers, there is little fluctuation in the toner particle diameter in the developer even if the toner balance for a long period of time is achieved, and good and stable developability can be obtained even with long-term stirring in the developing device. Even if the balance of the toner is carried out with the agent, fluctuations in the particle diameter of the toner are reduced, and there is no filming of the toner on the developing roller and no fusion of the toner to the member to the blade for thinning the toner. Even in the long-term use (stirring) of the developing device, good and stable developability can be obtained, so that a high-quality image can be obtained.

  The volume average particle diameter and the ratio (Dv / Dn) between the volume average particle diameter and the number average particle diameter are measured using, for example, a particle size measuring device “Multisizer II” manufactured by Beckman Coulter, Inc. Can do.

As said penetration, the penetration measured by the penetration test (JIS K2235-1991) needs to be 15 mm or more, for example, and 20-30 mm is more preferable.
When the penetration is less than 15 mm, the heat resistant storage stability may be deteriorated.
The penetration can be measured according to JIS K2235-1991. Specifically, a 50 ml glass container is filled with toner and left in a thermostatic bath at 50 ° C. for 20 hours. The penetration can be measured by cooling the toner to room temperature and performing a penetration test. In addition, it has shown that the said heat-resistant preservation | save property is excellent, so that the said penetration value is large.

As the low temperature fixability, from the viewpoint of achieving both a reduction in the fixing temperature and the occurrence of no offset, it is preferable that the lower limit temperature for fixing is lower, and more preferable that the temperature at which no offset is generated is higher. As a temperature range in which both can be achieved, the lower limit fixing temperature is less than 120 ° C., and the non-offset temperature is 200 ° C. or more.
The fixing lower limit temperature is, for example, an image forming apparatus, a transfer sheet is set, a copy test is performed, and the remaining ratio of the image density after rubbing the obtained fixed image with a pad is 70% or more. The fixing member temperature is the lower limit fixing temperature.
The offset non-occurrence temperature is adjusted such that the toner to be evaluated is developed with a predetermined amount by using an image forming apparatus, and is adjusted so that the temperature of the fixing member is variable, so that no offset is generated. Can be determined by measuring.

The thermal characteristics are also called flow tester characteristics, and are evaluated as, for example, a softening temperature (Ts), an outflow start temperature (Tfb), a 1/2 method softening point (T1 / 2), and the like.
These thermal characteristics can be measured by an appropriately selected method. For example, the thermal characteristics can be obtained from a flow curve measured using an elevated flow tester CFT500 type (manufactured by Shimadzu Corporation).
There is no restriction | limiting in particular as said softening temperature (Ts), According to the objective, it can select suitably, For example, 30 degreeC or more is preferable and 50-90 degreeC is more preferable. When the softening temperature (Ts) is less than 30 ° C., the heat resistant storage stability may be deteriorated.
There is no restriction | limiting in particular as said outflow start temperature (Tfb), According to the objective, it can select suitably, For example, 60 degreeC or more is preferable and 80-120 degreeC is more preferable. When the outflow start temperature (Tfb) is less than 60 ° C., at least one of heat resistant storage stability and offset resistance may be deteriorated.
The 1/2 method softening point (T1 / 2) is not particularly limited and may be appropriately selected depending on the intended purpose. For example, 90 ° C. or higher is preferable, and 100 to 170 ° C. is more preferable. When the 1/2 method softening point (T1 / 2) is less than 90 ° C., the offset resistance may be deteriorated.

There is no restriction | limiting in particular as said glass transition temperature, Although it can select suitably according to the objective, For example, 40-70 degreeC is preferable and 45-65 degreeC is more preferable. When the glass transition temperature (Tg) is less than 40 ° C., the heat-resistant storage stability of the toner may deteriorate, and when it exceeds 70 ° C., the low-temperature fixability may not be sufficient.
The glass transition temperature can be measured using, for example, a differential scanning calorimeter (“DSC-60”; manufactured by Shimadzu Corporation).

  The acid value of the toner is preferably, for example, 0.5 to 40.0 (KOH mg / g), and more preferably 3.0 to 35.0. By giving the toner an acid value, it becomes easy to be negatively charged.

The image density is, for example, preferably 1.40 or more, more preferably 1.45 or more, and 1.50 or more, as measured by a spectrometer (X-Light, 938 Spectrodensitometer). Is more preferable.
If the image density is less than 1.40, the image density may be low and high image quality may not be obtained.
The image density is determined by, for example, using a color electrophotographic apparatus (“IPSiO Color 8100”; manufactured by Ricoh Co., Ltd.) and a developer adhesion amount of 1.00 on copy paper (“Type 6200”; manufactured by Ricoh Co., Ltd.). A solid image of ± 0.1 mg / cm ² was formed with a surface temperature of the fixing roller of 160 ± 2 ° C., and the image density at any five positions in the obtained solid image was measured with a spectrometer (X-Light, 938). It can be measured by measuring with a spectrodensitometer and calculating the average value.

  The coloration of the toner of the present invention is not particularly limited and can be appropriately selected according to the purpose, and can be at least one selected from black toner, cyan toner, magenta toner and yellow toner. This toner can be obtained by appropriately selecting the type of the colorant.

The method for producing a toner of the present invention comprises preparing the oil-in-water dispersion by dispersing a solution or dispersion of the toner material as dispersed particles in an aqueous medium not containing the organic resin fine particles. Since the toner is granulated in the presence of the organic resin fine particles by adding the aqueous dispersion of the wax and the organic resin fine particles to the droplet dispersion, the wax having a small particle size can be used without using a dispersant or the like. The particles can be uniformly dispersed in the toner and can be appropriately present on the toner surface, preventing the uneven distribution of wax in the toner particles, excellent releasability, less filming, and high image quality. The resulting toner is produced efficiently.
In addition, the toner manufacturing method of the present invention comprises preparing an oil-in-water dispersion by dispersing the toner material solution or dispersion as fine dispersed particles in an aqueous medium, and then preparing the oil-in-water dispersion. Since the toner is granulated after the aqueous dispersion of the wax is added and the volume average particle size of the dispersed particles is increased, the composition of the material between the toner particles is uniform, and the chargeability and fixability And a toner having a small particle size and a narrow particle size distribution can be obtained.
Furthermore, in these toner production methods, since heating is not required, a wax having a low melting point can be used, and it is excellent in releasability at a low temperature and achieves both low-temperature fixability and heat-resistant storage stability. Toner is obtained.

  The toner of the present invention has a small particle size and a narrow particle size distribution, is excellent in releasability at low temperature, has little filming, and has both low-temperature fixability and heat-resistant storage stability to form a high-quality image. be able to. When the toner of the present invention contains particles containing at least the adhesive base material obtained by reacting the active hydrogen group-containing compound and a polymer capable of reacting with the active hydrogen group-containing compound in an aqueous phase, Excellent properties such as anti-aggregation, charging, fluidity, releasability, and fixing properties. Therefore, the toner of the present invention can be suitably used in various fields, and can be more suitably used for image formation by electrophotography. The following toner-containing container, developer, and process of the present invention are described below. It can be particularly suitably used for a cartridge, an image forming apparatus, and an image forming method.

(Developer)
The developer of the present invention contains at least the toner of the present invention and other components appropriately selected such as the carrier. The developer may be a one-component developer or a two-component developer. However, when it is used for a high-speed printer or the like corresponding to the recent improvement in information processing speed, the life is improved. In view of the above, the two-component developer is preferable.
In the case of the one-component developer using the toner according to the present invention, the toner particle diameter hardly fluctuates even if the balance of the toner is performed, and the filming of the toner on the developing roller or the toner is made thin. Therefore, toner is not fused 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. Further, in the case of the two-component developer using the toner of the present invention, even if the balance of the toner over a long period of time is performed, the fluctuation of the toner particle diameter in the developer is small, and even in the long-term stirring in the developing device, Good and stable developability can be obtained.

  There is no restriction | limiting in particular as said carrier, Although it can select suitably according to the objective, What has a core material and the resin layer which coat | covers this core material is preferable.

  There is no restriction | limiting in particular as a material of the said core material, It can select suitably from well-known things, For example, 50-90 emu / g manganese-strontium (Mn-Sr) type material, manganese-magnesium (Mn-) Mg) -based materials and the like are preferable, and high magnetization materials such as iron powder (100 emu / g or more) and magnetite (75 to 120 emu / g) are preferable in terms of securing image density. In addition, a weakly magnetized material such as a copper-zinc (Cu—Zn) -based (30 to 80 emu / g) is advantageous in that it can weaken the contact with the photoconductor in which the toner is in a spiked state and is advantageous in improving the image quality. Is preferred. These may be used alone or in combination of two or more.

The core material has a volume average particle diameter of preferably 10 to 150 μm, more preferably 40 to 100 μm.
When the average particle diameter (volume average particle diameter (D ₅₀ )) is less than 10 μm, the distribution of carrier particles may increase the number of fine powders, lower the magnetization per particle, and cause carrier scattering. If the thickness exceeds 150 μm, the specific surface area may decrease and toner scattering may occur. In the case of a full color having a large solid portion, the reproduction of the solid portion may be deteriorated.

  The material of the resin layer is not particularly limited and can be appropriately selected from known resins according to the purpose. For example, amino resins, polyvinyl resins, polystyrene resins, halogenated olefin resins, Polyester resin, polycarbonate resin, polyethylene resin, polyvinyl fluoride resin, polyvinylidene fluoride resin, polytrifluoroethylene resin, polyhexafluoropropylene resin, copolymer of vinylidene fluoride and acrylic monomer, vinylidene fluoride And a copolymer of vinyl fluoride, a fluoroterpolymer such as a terpolymer of tetrafluoroethylene, vinylidene fluoride, and a non-fluorinated monomer, and a silicone resin. These may be used individually by 1 type and may use 2 or more types together.

  Examples of the amino resin include urea-formaldehyde resin, melamine resin, benzoguanamine resin, urea resin, polyamide resin, and epoxy resin. Examples of the polyvinyl resin include acrylic resin, polymethyl methacrylate resin, poly Examples include acrylonitrile resin, polyvinyl acetate resin, polyvinyl alcohol resin, and polyvinyl butyral resin. Examples of the polystyrene resin include polystyrene resin and styrene acrylic copolymer resin. Examples of the halogenated olefin resin include polyvinyl chloride. Examples of the polyester resin include polyethylene terephthalate resin and polybutylene terephthalate resin.

  The resin layer may contain conductive powder or the like, if necessary. Examples of the conductive powder include metal powder, carbon black, titanium oxide, tin oxide, and zinc oxide. The average particle diameter of these conductive powders is preferably 1 μm or less. When the average particle diameter exceeds 1 μm, it may be difficult to control electric resistance.

For example, the resin layer is prepared by dissolving the silicone resin or the like in a solvent to prepare a coating solution, and then uniformly coating the coating solution on the surface of the core material by a known coating method, drying, and baking. It can be formed by doing. Examples of the coating method include a dipping method, a spray method, and a brush coating method.
There is no restriction | limiting in particular as said solvent, Although it can select suitably according to the objective, For example, toluene, xylene, methyl ethyl ketone, methyl isobutyl ketone, cersol butyl acetate, etc. are mentioned.
The baking is not particularly limited, and may be an external heating method or an internal heating method. For example, a stationary electric furnace, a fluid electric furnace, a rotary electric furnace, a burner furnace, etc. The method of using, the method of using a microwave, etc. are mentioned.

The amount of the resin layer in the carrier is preferably 0.01 to 5.0% by mass.
When the amount is less than 0.01% by mass, the uniform resin layer may not be formed on the surface of the core material. When the amount exceeds 5.0% by mass, the resin layer becomes thick. In some cases, granulation of carriers occurs, and uniform carrier particles may not be obtained.

  When the developer is the two-component developer, the content of the carrier in the two-component developer is not particularly limited and may be appropriately selected depending on the intended purpose. For example, 90 to 98% by mass Is preferable, and 93-97 mass% is more preferable.

Since the developer of the present invention contains the toner, it is excellent in transferability, fixability and the like, and can stably form a high-quality image.
The developer of the present invention can be suitably used for image formation by various known electrophotographic methods such as a magnetic one-component development method, a non-magnetic one-component development method, and a two-component development method. It can be particularly suitably used for containers, process cartridges, image forming apparatuses and image forming methods.

(Toner container)
The toner-containing container of the present invention is formed by filling the container of the toner of the present invention or the developer.
There is no restriction | limiting in particular as said container, It can select suitably from well-known things, For example, what has a container main body and a cap containing a toner etc. are mentioned suitably.
The size, shape, structure, material, etc. of the container body containing toner is not particularly limited and can be appropriately selected according to the purpose. For example, the shape is preferably cylindrical. The spiral surface irregularities are formed on the peripheral surface, and the toner as the contents can be transferred to the discharge port side by rotating, and part or all of the spiral part has a bellows function, etc. Is particularly preferred.
The material of the toner-containing container body is not particularly limited, and those having good dimensional accuracy are preferable. For example, a resin is preferably used. Among them, for example, polyester resin, polyethylene resin, polypropylene resin, polystyrene resin, Preferable examples include vinyl chloride resin, polyacrylic acid, polycarbonate resin, ABS resin, polyacetal resin, and the like.
The toner-containing container of the present invention is easy to store and transport, has excellent handleability, and is preferably used for replenishing toner by being detachably attached to the process cartridge and image forming apparatus of the present invention described later. Can do.

(Process cartridge)
The process cartridge of the present invention develops an electrostatic latent image carrier carrying an electrostatic latent image and the electrostatic latent image carried on the electrostatic latent image carrier using a developer to form a visible image. At least a developing means for forming the film, and other means appropriately selected as necessary.
The developing means includes a developer container that contains the toner or developer of the present invention, and a developer carrier that carries and transports the toner or developer contained in the developer container. And a layer thickness regulating member for regulating the thickness of the toner layer to be carried.
The process cartridge of the present invention can be detachably provided in various electrophotographic apparatuses, and is preferably detachably provided in the electrophotographic apparatus of the present invention described later.

(Image forming method and image forming apparatus)
The image forming method of the present invention includes at least an electrostatic latent image forming step, a developing step, a transfer step, and a fixing step, and further other steps appropriately selected as necessary, for example, a static elimination step, a cleaning step, Includes recycling and control processes.
The image forming apparatus of the present invention includes at least an electrostatic latent image carrier, an electrostatic latent image forming unit, a developing unit, a transfer unit, and a fixing unit, and further appropriately selected as necessary. It has other means, for example, static elimination means, cleaning means, recycling means, control means and the like.

-Electrostatic latent image forming step and electrostatic latent image forming means-
The electrostatic latent image forming step is a step of forming an electrostatic latent image on the electrostatic latent image carrier.
There are no particular restrictions on the material, shape, structure, size, etc. of the electrostatic latent image carrier (sometimes referred to as “photoconductive insulator” or “photoconductor”), and among the known ones The shape is preferably a drum shape, and examples of the material include inorganic photoconductors such as amorphous silicon and selenium, and organic photoconductors such as polysilane and phthalopolymethine. It is done. Among these, amorphous silicon and the like are preferable in terms of long life.

The formation of the electrostatic latent image can be performed, for example, by uniformly charging the surface of the electrostatic latent image carrier and then performing imagewise exposure, and is performed by the electrostatic latent image forming unit. be able to.
The electrostatic latent image forming means includes, for example, at least a charger that uniformly charges the surface of the electrostatic latent image carrier and an exposure device that exposes the surface of the electrostatic latent image carrier imagewise. Prepare.

The charging can be performed, for example, by applying a voltage to the surface of the electrostatic latent image carrier using the charger.
The charger is not particularly limited and may be appropriately selected depending on the purpose. For example, a known contact charging device including a conductive or semiconductive roll, brush, film, rubber blade, etc. And non-contact chargers utilizing corona discharge such as corotrons and corotrons.

The exposure can be performed, for example, by exposing the surface of the latent electrostatic image bearing member imagewise using the exposure device.
The exposure device is not particularly limited as long as it can expose the surface of the electrostatic latent image carrier charged by the charger so as to form an image to be formed, and is appropriately selected according to the purpose. For example, various exposure devices such as a copying optical system, a rod lens array system, a laser optical system, and a liquid crystal shutter optical system can be used.
In the present invention, a back light system in which imagewise exposure is performed from the back surface side of the electrostatic latent image carrier may be adopted.

-Development process and development means-
The developing step is a step of developing the electrostatic latent image using the toner or the developer of the present invention to form a visible image.
The visible image can be formed, for example, by developing the electrostatic latent image using the toner or the developer of the present invention, and can be performed by the developing unit.
The developing means is not particularly limited as long as it can be developed using, for example, the toner or developer of the present invention, and can be appropriately selected from known ones. For example, the toner of the present invention Preferably, a developer containing at least a developer and having at least a developing unit capable of contacting or non-contacting the toner or the developer with the electrostatic latent image is provided, and includes the toner container according to the present invention. More preferred is a developing device.

  The developing unit may be a dry developing type, a wet developing type, a single color developing unit, or a multicolor developing unit. For example, a toner having a stirrer for charging the toner or the developer by frictional stirring and a rotatable magnet roller is preferable.

  In the developing device, for example, the toner and the carrier are mixed and agitated, and the toner is charged by friction at that time, and held on the surface of the rotating magnet roller in a raised state to form a magnetic brush. . Since the magnet roller is disposed in the vicinity of the electrostatic latent image carrier (photoconductor), a part of the toner constituting the magnetic brush formed on the surface of the magnet roller is electrically attracted. It moves to the surface of the electrostatic latent image carrier (photoconductor) by force. As a result, the electrostatic latent image is developed with the toner, and a visible image is formed with the toner on the surface of the electrostatic latent image carrier (photoconductor).

  The developer accommodated in the developing device is a developer containing the toner of the present invention, but the developer may be a one-component developer or a two-component developer. The toner contained in the developer is the toner of the present invention.

-Transfer process and transfer means-
The transfer step is a step of transferring the visible image onto a recording medium. After the primary transfer of the visible image onto the intermediate transfer member using an intermediate transfer member, the visible image is transferred onto the recording medium. A primary transfer step of forming a composite transfer image by transferring a visible image onto an intermediate transfer body using two or more colors, preferably full color toner as the toner, and a composite transfer image; A mode including a secondary transfer step of transferring the transfer image onto the recording medium is more preferable.
The transfer can be performed, for example, by charging the latent electrostatic image bearing member (photoconductor) of the visible image using a transfer charger, and can be performed by the transfer unit. The transfer means includes a primary transfer means for transferring a visible image onto an intermediate transfer member to form a composite transfer image, and a secondary transfer means for transferring the composite transfer image onto a recording medium. Embodiments are preferred.
The intermediate transfer member is not particularly limited and may be appropriately selected from known transfer members according to the purpose. For example, a transfer belt and the like are preferable.

The transfer means (the primary transfer means, the secondary transfer means) is a transfer for peeling and charging the visible image formed on the electrostatic latent image carrier (photoconductor) to the recording medium side. It is preferable to have at least a vessel. There may be one transfer means or two or more transfer means.
Examples of the transfer device include a corona transfer device using corona discharge, a transfer belt, a transfer roller, a pressure transfer roller, and an adhesive transfer device.
The recording medium is not particularly limited and can be appropriately selected from known recording media (recording paper).

-Fixing process and fixing means-
The fixing step is a step of fixing the visible image transferred to the recording medium using a fixing unit, and may be performed each time the toner of each color is transferred to the recording medium, or for the toner of each color. You may perform this simultaneously in the state which laminated | stacked this.
The fixing unit is not particularly limited and may be appropriately selected depending on the intended purpose, but a known heating and pressing unit is preferable. Examples of the heating and pressing means include a combination of a heating roller and a pressure roller, a combination of a heating roller, a pressure roller, and an endless belt.
The heating in the heating and pressing means is usually preferably 80 ° C to 200 ° C.
In the present invention, for example, a known optical fixing device may be used together with or in place of the fixing step and the fixing unit depending on the purpose.

The neutralization step is a step of performing neutralization by applying a neutralization bias to the electrostatic latent image carrier, and can be suitably performed by a neutralization unit.
The neutralization means is not particularly limited, and may be appropriately selected from known neutralizers as long as it can apply a neutralization bias to the electrostatic latent image carrier. Preferably mentioned.

The cleaning step is a step of removing the electrophotographic toner remaining on the electrostatic latent image carrier, and can be suitably performed by a cleaning unit.
The cleaning means is not particularly limited as long as it can remove the electrophotographic toner remaining on the electrostatic latent image carrier, and can be appropriately selected from known cleaners. Suitable examples include brush cleaners, electrostatic brush cleaners, magnetic roller cleaners, blade cleaners, brush cleaners, web cleaners, and the like.

The recycling step is a step of recycling the electrophotographic color toner removed in the cleaning step to the developing unit, and can be suitably performed by the recycling unit.
There is no restriction | limiting in particular as said recycling means, A well-known conveyance means etc. are mentioned.

The control means is a process for controlling the respective steps, and can be suitably performed by the control means.
The control means is not particularly limited as long as the movement of each means can be controlled, and can be appropriately selected according to the purpose. Examples thereof include devices such as a sequencer and a computer.

  One mode for carrying out the image forming method of the present invention by the image forming apparatus of the present invention will be described with reference to FIG. An image forming apparatus 100 shown in FIG. 1 includes a photosensitive drum 10 (hereinafter referred to as “photosensitive member 10”) as the electrostatic latent image carrier, a charging roller 20 as the charging unit, and exposure as the exposure unit. The apparatus 30 includes a developing device 40 as the developing means, an intermediate transfer member 50, a cleaning device 60 as the cleaning means having a cleaning blade, and a static elimination lamp 70 as the static elimination means.

  The intermediate transfer member 50 is an endless belt, and is designed to be movable in the direction of an arrow by three rollers 51 that are arranged inside and stretched. Part of the three rollers 51 also functions as a transfer bias roller that can apply a predetermined transfer bias (primary transfer bias) to the intermediate transfer member 50. The intermediate transfer body 50 is provided with a cleaning device 90 having a cleaning blade in the vicinity thereof, and for transferring (secondary transfer) a developed image (toner image) to a transfer sheet 95 as a final transfer material. A transfer roller 80 serving as a transfer unit to which a transfer bias can be applied is disposed to face the transfer roller 80. Around the intermediate transfer member 50, a corona charger 52 for applying a charge to the toner image on the intermediate transfer member 50 is arranged between the photosensitive member 10 and the intermediate transfer member 50 in the rotation direction of the intermediate transfer member 50. It is disposed between the contact portion and the contact portion between the intermediate transfer member 50 and the transfer paper 95.

  The developing device 40 includes a black developing unit 45K, a yellow developing unit 45Y, a magenta developing unit 45M, and a cyan developing unit 45C that are disposed directly and oppositely around the photoreceptor 10. The black developing unit 45K includes a developer accommodating portion 42K, a developer supplying roller 43K, and a developing roller 44K. The yellow developing unit 45Y includes a developer accommodating portion 42Y, a developer supplying roller 43Y, and a developing roller 44Y. The magenta developing unit 45M includes a developer accommodating portion 42M, a developer supplying roller 43M, and a developing roller 44M, and the cyan developing unit 45C includes a developer accommodating portion 42C and a developer supplying roller 43C. And a developing roller 44C.

  In the image forming apparatus 100 shown in FIG. 1, for example, the charging roller 20 charges the photosensitive drum 10 uniformly. The exposure device 30 performs imagewise exposure on the photosensitive drum 10 to form an electrostatic latent image. The electrostatic latent image formed on the photosensitive drum 10 is developed by supplying toner from the developing device 40 to form a visible image (toner image). The visible image (toner image) is transferred (primary transfer) onto the intermediate transfer member 50 by the voltage applied from the roller 51, and further transferred (secondary transfer) onto the transfer paper 95. As a result, a transfer image is formed on the transfer paper 95. The residual toner on the photoconductor 10 is removed by the cleaning device 60, and the charge on the photoconductor 10 is temporarily removed by the charge eliminating lamp 70.

Another mode for carrying out the image forming method of the present invention by the image forming apparatus of the present invention will be described with reference to FIG. An image forming apparatus 100 shown in FIG. 2 is a tandem color image forming apparatus. The tandem image forming apparatus 100 includes a copying apparatus main body 150, a paper feed table 200, a scanner 300, and an automatic document feeder (ADF) 400.
The copying apparatus main body 150 is provided with an endless belt-like intermediate transfer member 50 at the center. The intermediate transfer member 50 is stretched around the support rollers 14, 15, and 16 and can be rotated clockwise in FIG. 2. An intermediate transfer member cleaning device 17 for removing residual toner on the intermediate transfer member 50 is disposed in the vicinity of the support roller 15. The intermediate transfer member 50 stretched between the support roller 14 and the support roller 15 is a tandem type in which four image forming units 18 of yellow, cyan, magenta, and black are arranged to face each other along the conveyance direction. A developing device 120 is disposed. An exposure device 21 is disposed in the vicinity of the tandem developing device 120. A secondary transfer device 22 is disposed on the side of the intermediate transfer member 50 opposite to the side on which the tandem developing device 120 is disposed. In the secondary transfer device 22, a secondary transfer belt 24, which is an endless belt, is stretched around a pair of rollers 23, and the transfer paper conveyed on the secondary transfer belt 24 and the intermediate transfer body 50 are in contact with each other. Is possible. A fixing device 25 is disposed in the vicinity of the secondary transfer device 22. The fixing device 25 includes a fixing belt 26 that is an endless belt, and a pressure roller 27 that is pressed against the fixing belt 26.
In the tandem image forming apparatus 100, a sheet reversing device 28 for reversing the transfer paper for image formation on both sides of the transfer paper is disposed in the vicinity of the secondary transfer device 22 and the fixing device 25. Yes.

  Next, formation of a full-color image (color copy) using the tandem developing device 120 will be described. That is, first, a document is set on the document table 130 of the automatic document feeder (ADF) 400, or the automatic document feeder 400 is opened and the document is set on the contact glass 32 of the scanner 300. 400 is closed.

  When a start switch (not shown) is pressed, when the document is set on the automatic document feeder 400, the document is transported and moved onto the contact glass 32, and then the document is set on the contact glass 32. Immediately after that, the scanner 300 is driven, and the first traveling body 33 and the second traveling body 34 travel. At this time, light from the light source is irradiated by the first traveling body 33 and reflected light from the document surface is reflected by the mirror in the second traveling body 34 and is received by the reading sensor 36 through the imaging lens 35 to be color. An original (color image) is read and used as black, yellow, magenta, and cyan image information.

  Each image information of black, yellow, magenta and cyan is stored in each image forming means 18 (black image forming means, yellow image forming means, magenta image forming means and cyan image forming means in the tandem developing device 120. ) And black, yellow, magenta and cyan toner images are formed in the respective image forming means. That is, each image forming means 18 (black image forming means, yellow image forming means, magenta image forming means, and cyan image forming means) in the tandem type developing device 120 is photosensitive as shown in FIG. On the basis of the body 10 (the black photoreceptor 10K, the yellow photoreceptor 10Y, the magenta photoreceptor 10M, and the cyan photoreceptor 10C), the charger 60 that uniformly charges the photoreceptor, and each color image information. The photosensitive member is exposed to each color image corresponding image (L in FIG. 3), and an electrostatic latent image corresponding to each color image is formed on the photosensitive member. A developing device 61 that develops using color toner (black toner, yellow toner, magenta toner, and cyan toner) to form a toner image of each color toner, and the toner image is transferred to the intermediate transfer member 5. The image forming apparatus includes a transfer charger 62 for transferring the image on the surface, a photoconductor cleaning device 63, and a static eliminator 64, and each monochrome image (black image, yellow image, magenta image) based on image information of each color. And cyan images) can be formed. The black image, the yellow image, the magenta image, and the cyan image formed in this way are formed on the black photoconductor 10K on the intermediate transfer member 50 that is rotationally moved by the support rollers 14, 15, and 16, respectively. The black image, the yellow image formed on the yellow photoconductor 10Y, the magenta image formed on the magenta photoconductor 10M, and the cyan image formed on the cyan photoconductor 10C are sequentially transferred (primary transfer). Is done. Then, the black image, the yellow image, the magenta image, and the cyan image are superimposed on the intermediate transfer member 50 to form a composite color image (color transfer image).

On the other hand, in the paper feed table 200, one of the paper feed rollers 142 is selectively rotated to feed out a sheet (recording paper) from one of the paper feed cassettes 144 provided in multiple stages in the paper bank 143. Each sheet is separated and sent to the paper feed path 146, transported by the transport roller 147, guided to the paper feed path 148 in the copying machine main body 150, and abutted against the registration roller 49 and stopped. Alternatively, the sheet feeding roller 150 is rotated to feed out the sheets (recording paper) on the manual feed tray 51, separated one by one by the separation roller 58, put into the manual feed path 53, and abutted against the registration roller 49 and stopped. . The registration roller 49 is generally used while being grounded, but may be used in a state where a bias is applied to remove paper dust from the sheet.
Then, the registration roller 49 is rotated in synchronization with the synthesized color image (color transfer image) synthesized on the intermediate transfer member 50, and a sheet (recording paper) is interposed between the intermediate transfer member 50 and the secondary transfer device 22. The secondary color transfer device 22 transfers the composite color image (color transfer image) onto the sheet (recording paper), thereby transferring the color image onto the sheet (recording paper). Is formed. The residual toner on the intermediate transfer member 50 after image transfer is cleaned by the intermediate transfer member cleaning device 17.

  The sheet (recording paper) on which the color image has been transferred is conveyed by the secondary transfer device 22 and sent to the fixing device 25, where the combined color image (color) is generated by heat and pressure. (Transfer image) is fixed on the sheet (recording paper). Thereafter, the sheet (recording paper) is switched by the switching claw 55 and discharged by the discharge roller 56 and stacked on the discharge tray 57, or switched by the switching claw 55 and reversed by the sheet reversing device 28 and transferred again. After being guided to the position and recording an image on the back surface, the image is discharged by the discharge roller 56 and stacked on the discharge tray 57.

  In the image forming apparatus and the image forming method of the present invention, the present invention achieves both low-temperature fixability and heat-resistant storage stability with a small particle size and narrow particle size distribution, excellent releasability at low temperatures, little filming. Therefore, high image quality can be obtained efficiently.

  Examples of the present invention will be described below, but the present invention is not limited to the following examples.

(Production Example 1)
-Preparation of aqueous dispersion of wax (wax dispersion) (1)-
200 parts by mass of paraffin wax (melting point 78 ° C.), 10 parts by mass of an anionic surfactant (Neogen SC), and 790 parts by mass of water are heated to 95 ° C., and a discharge pressure of 560 × 10 ⁵ N / m ² with a gorin homogenizer. The mixture was emulsified with water and then rapidly cooled to prepare an aqueous wax dispersion (wax dispersion) (1).
The volume average particle diameter (Dv) of the wax dispersion particles contained in the obtained wax dispersion liquid (1) is measured by a particle size distribution measuring apparatus (“LA-920”; manufactured by Horiba, Ltd.) using a laser light scattering method. As a result, it was 0.160 μm. The abundance of coarse particles having a volume average particle diameter (Dv) of 0.8 μm or more was 5% or less.

(Production Example 2)
-Preparation of aqueous dispersion of wax (wax dispersion) (2)-
200 parts by weight of paraffin wax (melting point: 68 ° C.), 10 parts by weight of anionic surfactant (Neogen SC), and 790 parts by weight of water are heated to 95 ° C., and a discharge pressure of 560 × 10 ⁵ N / m ² with a gorin homogenizer. The mixture was emulsified with water and rapidly cooled to prepare an aqueous wax dispersion (wax dispersion) (2).
The volume average particle diameter (Dv) of the wax dispersion particles contained in the obtained wax dispersion (2) is measured by a particle size distribution measuring apparatus (“LA-920”; manufactured by Horiba, Ltd.) using a laser light scattering method. As a result, it was 0.130 μm. The abundance of coarse particles having a volume average particle diameter (Dv) of 0.8 μm or more was 3% or less.

(Production Example 3)
-Preparation of aqueous dispersion of wax (wax dispersion) (3)-
200 parts by mass of a carbonyl group-containing wax (melting point: 82 ° C.), 10 parts by mass of an anionic surfactant (Neogen SC), and 790 parts by mass of water were heated to 130 ° C., and 560 × 10 ⁵ N / m ² with a gorin homogenizer. The mixture was emulsified at the discharge pressure and then rapidly cooled to prepare an aqueous wax dispersion (wax dispersion) (3).
The volume average particle diameter (Dv) of the wax dispersion particles contained in the obtained wax dispersion (3) is measured by a particle size distribution measuring apparatus (“LA-920”; manufactured by Horiba, Ltd.) using a laser light scattering method. As a result, it was 0.182 μm. The abundance of coarse particles having a volume average particle diameter (Dv) of 0.8 μm or more was 5% or less.

(Production Example 4)
-Preparation of aqueous dispersion of wax (wax dispersion) (4)-
200 parts by mass of a carbonyl group-containing wax (melting point: 116 ° C.), 10 parts by mass of an anionic surfactant (Neogen SC), and 790 parts by mass of water are heated to 130 ° C. and 560 × 10 ⁵ N / m ² with a gorin homogenizer. The mixture was emulsified at the discharge pressure and then rapidly cooled to prepare an aqueous wax dispersion (wax dispersion) (4).
The volume average particle diameter (Dv) of the wax dispersion particles contained in the obtained wax dispersion (4) is measured by a particle size distribution measuring apparatus (“LA-920”; manufactured by Horiba, Ltd.) using a laser light scattering method. As a result, it was 0.162 μm. The abundance of coarse particles having a volume average particle diameter (Dv) of 0.8 μm or more was 5% or less.

(Production Example 5)
-Preparation of aqueous dispersion of wax (wax dispersion) (5)-
The aqueous wax dispersion (wax dispersion) (1) produced in Production Example 1 was heated to 95 ° C., emulsified with a gorin homogenizer at a discharge pressure of 560 × 10 ⁵ N / m ² , and then rapidly cooled to obtain water of wax. A dispersion (wax dispersion) (5) was prepared.
The volume average particle diameter (Dv) of the wax dispersed particles contained in the obtained wax dispersion (5) is measured by a particle size distribution measuring apparatus (“LA-920”; manufactured by Horiba, Ltd.) using a laser light scattering method. As a result, it was 0.676 μm. The abundance of coarse particles having a volume average particle diameter (Dv) of 1.0 μm or more was 29%.

Example 1
<Oil-in-water dispersion preparation process>
An oil-in-water dispersion in which dispersed particles are dispersed was prepared as follows.

-Dissolution of toner material or preparation of dispersion-
--- Synthesis of unmodified polyester (low molecular weight polyester)-
229 parts by mass of bisphenol A ethylene oxide 2-mole adduct, 529 parts by mass of bisphenol A propion oxide 3-mole adduct, 208 parts by mass of terephthalic acid, 46 parts by mass of adipic acid And 2 parts by mass of dibutyltin oxide were added and reacted at 230 ° C. for 8 hours under normal pressure. Next, after reacting the reaction solution under a reduced pressure of 10 to 15 mmHg for 5 hours, 44 parts by mass of trimellitic anhydride was added to the reaction vessel, and the reaction was performed at 180 ° C. for 2 hours under normal pressure. A modified polyester was synthesized.
The obtained unmodified polyester had a number average molecular weight (Mn) of 2,500, a weight average molecular weight (Mw) of 6,700, a glass transition temperature (Tg) of 43 ° C., and an acid value of 25 mgKOH / g.

-Preparation of master batch (MB)-
1200 parts by mass of water, 540 parts by mass of carbon black (“Printex35”; manufactured by Degussa, DBP oil absorption = 42 ml / 100 g, pH = 9.5) as the colorant, and 1200 parts by mass of the unmodified polyester were added to Henschel. Mixing was performed using a mixer (Mitsui Mining Co., Ltd.). The mixture was kneaded for 30 minutes at 150 ° C. with two rolls, rolled and cooled, and pulverized with a pulverizer (manufactured by Hosokawa Micron) to prepare a master batch.

-Preparation of organic solvent phase-
500 parts by mass of the master batch and 500 parts by mass of ethyl acetate were charged into a reaction vessel in which a stir bar and a thermometer were set, and mixed for 1 hour to obtain a raw material solution.
1324 parts by mass of the obtained raw material solution was transferred to a reaction vessel, and using a bead mill (“Ultra Visco Mill”; manufactured by Imex Co., Ltd.), the liquid feeding speed was 1 kg / hr, the disk peripheral speed was 6 m / sec, and 0.5 mm zirconia. The carbon black was dispersed in 3 passes under the condition of 80% by volume of beads. Next, 1324 parts by mass of a 65% by mass ethyl acetate solution of the unmodified polyester was added to the dispersion. One pass was performed in a bead mill under the same conditions as described above, and the mixture was dispersed to prepare an organic solvent phase.
The solid content concentration (measurement condition: 130 ° C., by heating for 30 minutes) of the obtained organic solvent phase was 50% by mass.

--Synthesis of prepolymer--
In a reaction vessel equipped with a cooling tube, a stirrer and a nitrogen introduction tube, 410 parts by mass of the unmodified polyester, 89 parts by mass of isophorone diisocyanate, and 500 parts by mass of ethyl acetate were charged and reacted at 100 ° C. for 5 hours. A prepolymer (polymer capable of reacting with the active hydrogen group-containing compound) was synthesized.
The free isocyanate content of the obtained prepolymer was 1.53% by mass.

--Synthesis of ketimine (the active hydrogen group-containing compound)-
In a reaction vessel equipped with a stir bar and a thermometer, 170 parts by mass of isophoronediamine and 75 parts by mass of methyl ethyl ketone were charged and reacted at 50 ° C. for 5 hours to synthesize a ketimine compound (the active hydrogen group-containing compound).
The amine value of the obtained ketimine compound (the active hydrogen machine-containing compound) was 418.

  In a reaction vessel, 749 parts by mass of the organic solvent phase, 115 parts by mass of the prepolymer, and 2.9 parts by mass of the ketimine compound were charged, and 7.5 m / m using a TK homomixer (manufactured by Tokushu Kika Kogyo Co., Ltd.). The mixture was mixed at s for 1 minute to prepare a toner material solution or dispersion.

-Preparation of aqueous medium phase-
990 parts by mass of water, 37 parts by mass of a 48.5% by mass aqueous solution of sodium dodecyl diphenyl ether disulfonate (“Eleminol MON-7”; manufactured by Sanyo Chemical Industries) and 90 parts by mass of ethyl acetate were mixed and stirred to give a milky white liquid ( An aqueous medium phase) was obtained.

-Emulsification or dispersion-
1200 parts by mass of the aqueous medium phase is added to the dissolved or dispersed liquid of the toner material and mixed for 20 minutes at a peripheral speed of 15 m / s with a TK homomixer (manufactured by Tokushu Kika Kogyo Co., Ltd.). A mold dispersion (emulsified slurry) was prepared.
The particle size of the dispersed particles in the obtained oil-in-water dispersion (emulsified slurry) was measured using a particle size distribution measuring device (“nanotrac UPA-150EX”; manufactured by Nikkiso Co., Ltd.), and found to be 0.392 μm. there were.

<Toner granulation process>
-Preparation of organic resin fine particle dispersion-
In a reaction vessel in which a stir bar and a thermometer are set, 683 parts by mass of water, 20 parts by mass of a sodium salt of ethylene oxide methacrylate adduct sulfate ("Eleminol RS-30" manufactured by Sanyo Chemical Industries), 78 parts by mass of styrene , 78 parts by mass of methacrylic acid, 120 parts by mass of butyl acrylate, and 1 part by mass of ammonium persulfate were added and stirred at 400 rpm for 15 minutes to obtain a white emulsion. The emulsion was heated to raise the system temperature to 75 ° C. and reacted for 5 hours. Next, 30 parts by mass of a 1% by mass ammonium persulfate aqueous solution was added, and the mixture was aged at 75 ° C. for 5 hours. Vinyl resin particles (styrene-methacrylic acid-butyl acrylate-methacrylic acid ethylene oxide adduct sulfate sodium salt) (Copolymer) aqueous dispersion (organic resin fine particle dispersion) was prepared.
The volume average particle diameter (Dv) of the organic resin fine particles contained in the obtained organic resin fine particle dispersion was measured by a particle size distribution measuring device (“nanotrac UPA-150EX”; manufactured by Nikkiso Co., Ltd.), and found to be 55 nm. . Moreover, when a part of the organic resin fine particle dispersion was dried to isolate the resin, and the glass transition temperature (Tg) of the resin was measured, it was 48 ° C. and the weight average molecular weight (Mw) was measured. It was 450,000.

-Controlling the particle size of dispersed particles-
Using a paddle type stirring device, the oil-in-water dispersion (emulsified slurry) was stirred at a peripheral speed of 0.7 m / s, and the water dispersion (1) of the wax obtained in Production Example 1 was 15 masses. And 15 parts by mass of the organic resin fine particles were added, and further 80 parts by mass of a 10% by mass sodium chloride solution was added to control the particle size of the dispersed particles in the emulsified slurry.

-Removal of organic solvent-
The emulsified slurry after particle size control was charged into a reaction vessel equipped with a stirrer and a thermometer, and after removing the solvent at 30 ° C. for 8 hours, aging was carried out at 45 ° C. for 4 hours to obtain a dispersed slurry.
When the volume average particle size and number average particle size of the obtained dispersion slurry were measured with Multisizer III (manufactured by Beckman Coulter, Inc.), the volume average particle size was 4.3 μm, and the number average particle size was 3.8 μm. It was.

-Cleaning and drying-
After 100 parts by mass of the dispersion slurry was filtered under reduced pressure, 100 parts by mass of ion-exchanged water was added to the filter cake, mixed with a TK homomixer (10 minutes at a rotation speed of 10.0 m / s), and then filtered. To the obtained filter cake, 100 parts by mass of ion-exchanged water was added, mixed with a TK homomixer (for 10 minutes at a rotation speed of 10.0 m / s), and then filtered under reduced pressure. 100 parts by mass of a 10% by mass aqueous sodium hydroxide solution was added to the obtained filter cake, mixed with a TK homomixer (at a rotation speed of 10.0 m / s for 10 minutes), and then filtered. To the obtained filter cake, 300 parts by mass of ion-exchanged water was added, mixed with a TK homomixer (at a rotation speed of 10.0 m / s for 10 minutes), and then filtered twice to obtain a final filter cake. It was.
The obtained final filter cake was dried with a circulating dryer at 45 ° C. for 48 hours, and sieved with an opening of 75 μm mesh to obtain toner base particles of Example 1.

-External additive treatment-
Henschel mixer (manufactured by Mitsui Mining Co., Ltd.) was used with 100 parts by mass of the obtained toner base particles of Example 1 using 1.5 parts by mass of hydrophobic silica as an external additive and 0.5 parts by mass of hydrophobic titanium oxide. The toner of Example 1 was produced by mixing and sieving with a mesh having a mesh size of 35 μm.

  With respect to the obtained toner, the volume average particle size (Dv), number average particle size (Dn), and particle size distribution (volume average particle size (Dv) / number average particle size (Dn)) were measured by the following methods. The results are shown in Table 1.

<Toner particle size>
The volume average particle diameter (Dv) of the toner and the number average particle diameter (Dn) of the toner were measured using a particle size measuring device (“Multisizer II”; manufactured by Beckman Coulter, Inc.) with an aperture diameter of 100 μm. From these results, the particle size distribution (volume average particle diameter (Dv) / number average particle diameter (Dn)) was calculated.

(Example 2)
In Example 1, the wax aqueous dispersion (1) obtained in Production Example 2 was replaced with the wax aqueous dispersion (2) obtained in Production Example 3 in the same manner as in Example 1. The toner of Example 2 was produced. Further, various physical properties were measured in the same manner as in Example 1. The results are shown in Table 1.
In addition, the particle size of the dispersed particles in the oil-in-water dispersion (emulsified slurry) obtained in the oil-in-water dispersion preparation step was determined using a particle size distribution measuring device (“nanotrac UPA-150EX”; manufactured by Nikkiso Co., Ltd.). ) Was 0.392 μm.
Next, using a paddle type stirring device, the oil-in-water dispersion (emulsified slurry) was stirred at a peripheral speed of 0.7 m / s, and the aqueous dispersion of wax obtained in Production Example 3 (2 ) 15 parts by mass and 15 parts by mass of the organic resin fine particles are added, and further 80 parts by mass of a 10% by mass sodium chloride solution is added to control the particle size of the dispersed particles in the emulsified slurry. Was measured using the particle size distribution measuring apparatus (“nanotrac UPA-150EX”; manufactured by Nikkiso Co., Ltd.), it was 5.1 μm.

(Example 3)
In Example 1, the wax aqueous dispersion (1) obtained in Production Example 1 was replaced with the wax aqueous dispersion (3) obtained in Production Example 3 in the same manner as in Example 1. The toner of Example 3 was produced. Further, various physical properties were measured in the same manner as in Example 1. The results are shown in Table 1.

(Example 4)
In Example 1, the wax aqueous dispersion (1) obtained in Production Example 1 was replaced with the wax aqueous dispersion (4) obtained in Production Example 4 in the same manner as in Example 1. The toner of Example 4 was produced. Further, various physical properties were measured in the same manner as in Example 1. The results are shown in Table 1.

(Example 5)
In Example 1, the wax aqueous dispersion (1) obtained in Production Example 1 was replaced with the wax aqueous dispersion (5) obtained in Production Example 5 in the same manner as in Example 1. The toner of Example 5 was produced. Further, various physical properties were measured in the same manner as in Example 1. The results are shown in Table 1.

(Example 6)
Example 1 except that in Example 1, the dissolution or dispersion of the toner material in the oil-in-water dispersion preparation step was prepared by the following method, and the control of the dispersed particles in the toner granulation step was performed by the following method. The toner of Example 6 was produced in the same manner as described above. Further, various physical properties were measured in the same manner as in Example 1. The results are shown in Table 1.

<Oil-in-water dispersion preparation process>
-Dissolution of toner material or preparation of dispersion-
In a reaction vessel, 749 parts by mass of the organic solvent phase, 115 parts by mass of the prepolymer, 2.9 parts by mass of the ketimine compound, and a tertiary amine compound (“U-CAT 660M”; manufactured by San Apro Co., Ltd.) 3 Then, 5 parts by mass was charged, and a TK homomixer (manufactured by Tokushu Kika Kogyo Co., Ltd.) was used for 1 minute at 7.5 m / s to prepare a toner material solution or dispersion.

-Emulsification or dispersion-
1200 parts by mass of the aqueous medium phase is added to the obtained toner material dissolved or dispersed, and mixed with a TK homomixer (made by Tokushu Kika Kogyo Co., Ltd.) at a peripheral speed of 15 m / s for 20 minutes. An oil droplet type dispersion (emulsified slurry) was prepared.
When the particle size of the dispersed particles in the obtained oil-in-water dispersion (emulsified slurry) was measured using a particle size distribution measuring device (“nanotrac UPA-150EX”; manufactured by Nikkiso Co., Ltd.), it was 0.401 μm. there were.

<Toner granulation process>
-Controlling the particle size of dispersed particles-
Using a paddle type stirring device, the oil-in-water dispersion (emulsified slurry) was stirred at a peripheral speed of 0.7 m / s, and the water dispersion (1) of the wax obtained in Production Example 1 was 15 masses. And 120 parts by mass of 10 parts by mass and 10% by mass sodium chloride solution were added. This was charged into a reaction vessel in which a stirrer and a thermometer were set, and 10 parts by mass of a 20% by mass aqueous solution of sodium dodecylbenzenesulfonate (“Neogen SC-A”; manufactured by Daiichi Kogyo Seiyaku) was added. The particle size of the dispersed particles in the emulsified slurry was controlled. The particle size of the dispersed particles was measured using the particle size distribution analyzer (“nanotrac UPA-150EX”; manufactured by Nikkiso Co., Ltd.) and found to be 5.3 μm.

(Comparative Example 1)
In Example 1, in the toner granulation step, the organic solvent phase used in the preparation of the dissolution or dispersion of the toner material in the oil-in-water dispersion preparation step is replaced with the organic solvent phase prepared by the following method. A toner of Comparative Example 1 was produced in the same manner as in Example 1 except that the aqueous dispersion (1) of the wax prepared in Production Example 1 was not added. Further, various physical properties were measured in the same manner as in Example 1. The results are shown in Table 1.

<Oil-in-water dispersion preparation process>
-Dissolution of toner material or preparation of dispersion-
-Preparation of organic solvent phase-
In a reaction vessel in which a stir bar and a thermometer were set, 378 parts by mass of the unmodified polyester, 110 parts by mass of carnauba wax, 22 parts by mass of CCA (“salicylic acid metal complex E-84”; manufactured by Orient Kogyo), and ethyl 947 A mass part was charged, the temperature was raised to 80 ° C. with stirring, the temperature was kept at 80 ° C. for 5 hours, and then cooled to 30 ° C. over 1 hour. Next, 500 parts by mass of the master batch and 500 parts by mass of ethyl acetate were charged into the reaction vessel and mixed for 1 hour to obtain a raw material solution.
1324 parts by mass of the obtained raw material solution was transferred to a reaction vessel, and using a bead mill (“Ultra Visco Mill”; manufactured by Imex Co., Ltd.), the liquid feeding speed was 1 kg / hr, the disk peripheral speed was 6 m / sec, and 0.5 mm zirconia. The carbon black and the carnauba wax were dispersed in 3 passes under the condition of 80% by volume of beads. Next, 1324 parts by mass of a 65% by mass ethyl acetate solution of the unmodified polyester was added to the dispersion. One pass was performed in a bead mill under the same conditions as described above, and the mixture was dispersed to prepare an organic solvent phase.
The solid content concentration (measurement condition: 130 ° C., by heating for 30 minutes) of the obtained organic solvent phase was 50% by mass.

  After the toner material was dissolved or dispersed using the organic solvent phase obtained, the aqueous medium was added to the toner material dissolved or dispersed in the same manner as in Example 1 to perform emulsification or dispersion. Then, an oil-in-water dispersion (emulsified slurry) was prepared. Thereafter, the toner was granulated without adding with the water dispersion (1) of the wax, and the organic solvent was removed, washed and dried in the same manner as in Example 1 to obtain the toner base particles of Comparative Example 1. Then, the toner base particles were subjected to the external additive treatment to produce a toner of Comparative Example 1.

  Next, 2.5 parts by mass of each of the toners of Examples 1 to 6 and Comparative Example 1 having been subjected to external additive treatment and 97.5 parts by mass of a silicone-coated ferrite carrier (core material particle size: 45 μm) The developers in Examples 1 to 6 and Comparative Example 1 were produced.

  Using each developer thus obtained, (a) fixability, (b) heat resistant storage stability, (c) filming resistance, (d) image density, (e) wax dispersibility, And (f) The overall evaluation was measured. The results are shown in Table 2.

(A) Fixability (offset generation temperature and fixing lower limit temperature)
Using a color electrophotographic apparatus ("IPSiO Color 8100"; manufactured by Ricoh Co., Ltd.), which is tuned by modifying it to an oilless fixing system, transfer paper ("Type 6000-70W"; manufactured by Ricoh Co., Ltd.), and transfer paper (“Type 6200”; manufactured by Ricoh Co., Ltd.) was used to evaluate fixability (offset non-occurrence temperature and fixing lower limit temperature).

<Offset generation temperature>
Image formation was performed using the color electrophotographic apparatus on the transfer paper (“Type 6000-70W”; manufactured by Ricoh Co., Ltd.) on each single color of yellow, magenta, cyan, and black, and red, blue, The green solid image was adjusted so that 1.0 ± 0.1 mg / cm ² of toner was developed for each single color. The obtained image was fixed by changing the temperature of the fixing belt (heating roller), and the temperature at which no offset occurred (temperature at which no offset occurred) was measured.

<Fixing temperature limit>
For the image, using the color electrophotographic apparatus, the transfer paper (“Type 6200”; manufactured by Ricoh Co., Ltd.) was set, and a copy test was performed. The fixing roll temperature at which the residual ratio of the image density after rubbing the obtained fixed image with a pad was 70% or more was determined as the minimum fixing temperature.
The low temperature fixability was evaluated based on the following criteria.
〔Evaluation criteria〕
A: The lower limit fixing temperature is less than 100 ° C. O: The lower limit fixing temperature is 100 ° C. or higher and lower than 110 ° C. Δ: The lower limit fixing temperature is 110 ° C. or higher and lower than 120 ° C.

(B) Heat-resistant storage stability A 50 cc glass container was filled with toner and left in a constant temperature bath at 50 ° C. for 20 hours. The toner was cooled to room temperature, and the penetration was measured by a penetration test (JIS K2235-1991). The greater the penetration, the better the heat resistant storage stability, and the less blocking occurs. Using the penetration, the heat resistant storage stability was evaluated based on the following criteria.
〔Evaluation criteria〕
◎: Needle penetration 20 mm or more ○: Needle penetration 15 mm or more and less than 20 mm △: Needle penetration 10 mm or more and less than 15 mm ×: Needle penetration less than 10 mm

(C) Filming resistance The state of occurrence of toner filming on the developing roller or photoconductor when copying 50,000 sheets using a color electrophotographic apparatus (“IPSiO Color 8100”; manufactured by Ricoh Co., Ltd.) The presence or absence of was visually observed and evaluated based on the following criteria.
〔Evaluation criteria〕
◎: Filming is not observed ○: Line-shaped filming is hardly observed Δ: Line-shaped filming is partially observed ×: Filming is generally observed

(D) Image density Using a color electrophotographic apparatus (“IPSiO Color 8100”; manufactured by Ricoh Co., Ltd.), the amount of each developer adhered to transfer paper (“Type 6200”; manufactured by Ricoh Co., Ltd.) is 1.00 ±. A solid image of 0.1 mg / cm ² was formed at a surface temperature of the fixing roller of 160 ± 2 ° C. The image density of arbitrary 5 places in the obtained solid image was measured using a spectrometer (“938 Spectrodensitometer, manufactured by X-Rite”). The obtained image density value was evaluated based on the following criteria: The higher the obtained image density value, the higher the image density, and the higher the density image can be formed.
〔Evaluation criteria〕
○: Image density value is 1.4 or more ×: Image density value is less than 1.4

(F) Dispersibility of wax The dispersibility of the wax was evaluated based on the following criteria by observing the toner with an electron microscope.
〔Evaluation criteria〕
○: No variation Δ: Some variation ×: Large variation

(F) Comprehensive evaluation Comprehensive evaluation was performed based on the following reference | standard from the result of all the said performance evaluations.
〔Evaluation criteria〕
◎: Overall excellent state ○: Overall good state △: Overall slightly inferior state ×: Overall poor state

From the results of Tables 1 and 2, the following is clear. That is, in Examples 1 to 6, since the aqueous dispersion of the wax is added during the dissolution or dispersion of the toner material in the aqueous medium, the small particle size and the particle size distribution are narrow. A toner having good wax dispersibility was obtained. In addition, the toner is excellent in releasability at low temperature, has little filming, has both low-temperature fixability and heat-resistant storage stability, has good image density evaluation results, and can obtain high image quality. understood.
On the other hand, since the toner obtained in Comparative Example 1 did not use an aqueous dispersion of wax, the dispersibility of the wax was poor and the occurrence of filming was observed. Further, it was found that the low-temperature fixability and heat-resistant storage stability were inferior, the image density evaluation results were poor, and high image quality could not be obtained.

The toner production method of the present invention can efficiently obtain a toner having a small particle size, a narrow particle size distribution, and good wax dispersibility.
The toner of the present invention is suitably used for high-quality image formation because it has excellent releasability at low temperatures, has little filming, and achieves both low-temperature fixability and heat-resistant storage stability. The developer, toner-containing container, process cartridge, image forming apparatus and image forming method of the present invention using the toner of the present invention are suitably used for high-quality image formation.

FIG. 1 is a schematic explanatory view showing an example in which the image forming method of the present invention is carried out by the image forming apparatus of the present invention. FIG. 2 is a schematic explanatory view showing an example of carrying out the image forming method of the present invention by the image forming apparatus (tandem color image forming apparatus) of the present invention. FIG. 3 is a partially enlarged schematic explanatory view of the image forming apparatus shown in FIG.

Explanation of symbols

10 Photoconductor (Photoconductor drum)
10K black photoconductor 10Y yellow photoconductor 10M magenta photoconductor 10C cyan photoconductor 14 support roller 15 support roller 16 support roller 17 intermediate transfer cleaning device 18 image forming means 20 charging roller 21 exposure device 22 secondary transfer device 23 Roller 24 Secondary transfer belt 25 Fixing device 26 Fixing belt 27 Pressure roller 28 Sheet reversing device 30 Exposure device 32 Contact glass 33 First traveling member 34 Second traveling member 35 Imaging lens 36 Reading sensor 40 Developing device 41 Developing belt 42K Developer container 42Y Developer container 42M Developer container 42C Developer container 43K Developer supply roller 43Y Developer supply roller 43M Developer supply roller 43C Developer supply roller 44K Developer roller 44Y Developer roller 44M Developer Roller 44C Development roller 45K Black development unit 45Y Yellow development unit 45M Magenta development unit 45C Cyan development unit 49 Registration roller 50 Intermediate transfer member 51 Roller 52 Corona charger 53 Constant current source 55 Switching claw 56 Discharge roller 57 Discharge tray 58 Separating roller 60 Cleaning device 61 Developing device 62 Transfer charger 63 Photoconductor cleaning device 64 Static eliminator 70 Static elimination lamp 80 Transfer roller 90 Cleaning device 95 Transfer paper 100 Image forming device 110 Belt type fixing device 120 Tandem type developing device 130 Document table 142 paper feed roller 143 paper bank 144 paper feed cassette 145 separation roller 146 paper feed path 147 transport roller 148 paper feed path 150 copying machine main body 200 paper feed table 300 scanner 400 automatic document Conveyor (ADF)

Claims (18)

The toner material is dissolved or dispersed in an organic solvent to prepare a solution or dispersion of the toner material, and the dissolved or dispersed liquid is dispersed as dispersed particles in an aqueous medium that does not contain organic resin fine particles. A method for producing a toner comprising preparing a dispersion and then adding a water dispersion of wax and organic resin fine particles to the oil-in-water dispersion to granulate the toner in the presence of the organic resin fine particles , The toner material includes at least an active hydrogen group-containing compound and a polymer capable of reacting with the active hydrogen group-containing compound,
By granulating, by reacting the active hydrogen group-containing compound and a polymer capable of reacting with the active hydrogen group-containing compound to produce an adhesive base material, particles containing at least the adhesive base material are obtained. A method for producing toner, comprising: A toner material is dissolved or dispersed in an organic solvent to prepare a solution or dispersion of the toner material, and the dissolved or dispersed liquid is dispersed as dispersed particles having a volume average particle diameter of 0.1 to 3 μm in an aqueous medium. After preparing an oil-in-water dispersion, an aqueous dispersion of wax is added to the oil-in-water dispersion and the volume average particle size of the dispersed particles is increased to 3 to 9 μm before granulating the toner. The toner material includes at least an active hydrogen group-containing compound and a polymer capable of reacting with the active hydrogen group-containing compound,
By granulating, by reacting the active hydrogen group-containing compound and a polymer capable of reacting with the active hydrogen group-containing compound to produce an adhesive base material, particles containing at least the adhesive base material are obtained. A method for producing toner, comprising: A toner material is dissolved or dispersed in an organic solvent to prepare a solution or dispersion of the toner material, and the dissolved or dispersed liquid is 0.1 to 3 μm in volume average particle size in an aqueous medium not containing organic resin fine particles. After preparing an oil-in-water dispersion by dispersing as dispersed particles of water, an aqueous dispersion of wax and organic resin fine particles are added to the oil-in-water dispersion to disperse the dispersion in the presence of the organic resin fine particles. A toner manufacturing method in which a toner is granulated after increasing a volume average particle diameter of particles to 3 to 9 μm , wherein the toner material can react with the active hydrogen group-containing compound and the active hydrogen group-containing compound. Including at least a polymer,
By granulating, by reacting the active hydrogen group-containing compound and a polymer capable of reacting with the active hydrogen group-containing compound to produce an adhesive base material, particles containing at least the adhesive base material are obtained. A method for producing toner, comprising: A toner material is dissolved or dispersed in an organic solvent to prepare a solution or dispersion of the toner material, and the dissolved or dispersed liquid is dispersed as dispersed particles in an aqueous medium to prepare an oil-in-water dispersion. A method for producing a toner , comprising adding an aqueous dispersion of wax to the oil-in-water dispersion and increasing the volume average particle size of the dispersed particles to 3 to 45 times, and then granulating the toner, The toner material includes at least an active hydrogen group-containing compound and a polymer capable of reacting with the active hydrogen group-containing compound, and the granulation is capable of reacting with the active hydrogen group-containing compound and the active hydrogen group-containing compound. A method for producing a toner, which is performed by reacting a polymer to produce an adhesive base material and obtaining particles containing at least the adhesive base material.   The toner production method according to claim 4, wherein the volume average particle diameter of the dispersed particles before the increase is 0.1 to 3 μm, and the volume average particle diameter of the dispersed particles after the increase is 3 to 9 μm. The method for producing a toner according to claim 1, wherein the volume average particle diameter of the wax dispersed particles in the aqueous dispersion of wax is 0.1 to 2 μm. The method for producing a toner according to claim 1, wherein the solution or dispersion of the toner material contains a wax, and the wax is dispersed in the solution or dispersion. The method for producing a toner according to claim 1, wherein the wax has a melting point of 50 to 90 ° C. The method for producing a toner according to claim 1, wherein the wax is paraffin wax. 4. The toner production method according to claim 1, wherein an ionizing agent is added together with the organic resin fine particles when the organic resin fine particles are added. The method for producing a toner according to claim 10, wherein the ionizing agent is at least one selected from a salt composed of a monovalent cation and a monovalent anion. The method for producing a toner according to claim 11, wherein the monovalent cation contains at least one of a sodium ion and a potassium ion. The method for producing a toner according to claim 1, wherein the toner material is dissolved or dispersed in an aqueous medium with stirring. When the stirring speed during dissolution of the toner material or dispersion in the aqueous medium is Am / s and the stirring speed when the toner is granulated is Bm / s, the following formula is given: 7 <A < The toner production method according to claim 1, wherein the toner satisfies the following conditions: 23 and 1.4 <A / B <100. The method for producing a toner according to claim 2, wherein the volume average particle diameter of the dispersed particles before the increase is 0.1 to 2 μm. A toner manufactured by the toner manufacturing method according to claim 1. The toner according to claim 16, wherein the adhesive substrate contains a polyester resin. An electrostatic latent image forming step of forming an electrostatic latent image on the electrostatic latent image carrier, and developing the electrostatic latent image with the toner according to any one of claims 16 to 17 to form a visible image An image forming method comprising: a developing step for forming the image; a transfer step for transferring the visible image to a recording medium; and a fixing step for fixing the transferred image transferred to the recording medium.

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