Patent Application
20090053640
The present invention relates to a toner used, e.g., in copiers, laser printers, plain paper facsimiles, color PPCs, color laser printers, color facsimiles or multifunctional devices, and a method for producing the toner.
In recent years, the use of image forming apparatuses such as a printer has been shifting increasingly from office to personal purposes, and there is a growing demand for technologies that can achieve, e.g., a small size, a high speed, high image quality, or high reliability for those apparatuses. Under such circumstances, a cleanerless process, a tandem color process, and oilless fixing are required along with better maintainability and less ozone emission. The cleanerless process allows residual toner from the transfer to be recycled for development without cleaning in an electrophotographic system. The tandem color process enables high-speed output of color images. The oilless fixing can provide clear color images with high glossiness, high transmittance, and offset resistance, even if no fixing oil is used to prevent offset during fixing. All of these functions should be performed at the same time, and therefore improvements in the toner characteristics as well as the processes are important factors.
In a fixing process for color images of a color printer, it is necessary for each color of toner to be melted and mixed sufficiently to increase the transmittance. In this case, a melt failure of the toner may cause light scattering on the surface or the inside of the toner image, and thus affects the original color of the toner pigment. Moreover, light does not reach the lower layer of the superimposed images, resulting in poor color reproduction. Therefore, the toner should have a complete melting property and transmittance high enough not to reduce the original color. In particular, the need for light transmittance for an OHP sheet is increasing with an increase in opportunities to give a color presentation.
During the formation of color images, the toner may adhere to the surface of a fixing roller and cause offset. Therefore, a large amount of oil or the like should be applied to the fixing roller, which makes the handling or configuration of equipment more complicated. Thus, oilless fixing (no oil is used for fixing) is required to provide compact, maintenance-free, and low-cost equipment. To achieve the oilless fixing, e.g., a toner having a configuration in which a release agent (wax) is added to a binder resin with a sharp melting property is being put to practical use.
However, such a toner is very prone to a transfer failure or toner image disturbance during transfer because of its strong cohesiveness. Therefore, it is difficult to ensure the compatibility between transfer and fixing. When the toner is used as a two-component developer, so-called spent, in which a low-melting component of the toner adheres to the surface of a carrier, is likely to occur due to heat generated by mechanical collision or friction between the particles of the toner and the carrier or between the particles and the developing unit. This decreases the charging ability of the carrier for the toner and interferes with a longer life of the two-component developer.
Even with pulverization and classification of the conventional kneading and pulverizing processes, the actual particle size can be reduced to only about 8 μm in view of the economic and performance conditions. At present, various methods are considered to produce a toner having a smaller particle size. Moreover, a method for achieving the oilless fixing by adding a release agent (wax) to a resin with a low softening property during melting and kneading also is considered. However, there is a limit to the amount of wax that can be added, and increasing the amount of wax may cause problems such as low flowability of the toner, transfer voids, and filming of the toner on a photoconductive member.
Therefore, various ways of polymerization other than the kneading and pulverizing processes have been studied as a method for producing a toner. For example, a toner may be produced by suspension polymerization. In this method, however, it is difficult to control the particle size distribution of the toner to be narrower than that of a toner produced by the kneading and pulverizing processes, and in many cases further classification is necessary, Moreover, since the toner obtained by this method is almost spherical in shape, the toner remaining on the photoconductive member or the like cannot be cleaned successfully, and thus the reliability of the image quality is reduced.
Also, a toner may be produced by emulsion polymerization. This method includes the following steps: preparing an aggregated particle dispersion by forming aggregated particles (also referred to as core particles) in a dispersion in which at least resin particles and colorant particles are dispersed; adding a resin particle dispersion in which resin particles are dispersed to the aggregated particle dispersion and mixing them so that the resin particles adhere to the aggregated particles to form adhesive particles; and heating and fusing the adhesive particles.
Patent Document 1 discloses a process of preparing a liquid mixture by mixing at least a resin particle dispersion in which resin particles are dispersed in a surface-active agent having a polarity and a colorant particle dispersion in which colorant particles are dispersed in a surface-active agent having a polarity. The surface-active agents included in the liquid mixture have the same polarity, so that a toner for electrostatic charge image development with high reliability and excellent charge and color development properties can be produced in a simple and easy manner.
Patent Document 2 discloses a release agent including at least one type of ester composed of at least one selected from higher alcohol having a carbon number of 12 to 30 and higher fatty acid having a carbon number of 12 to 30, and binder resin particles including at least two types of resin particles with different molecular weights. This configuration can provide a toner with an excellent fixing property, color development property, transparency, and color mixing property.
As the release agent, e.g., low molecular-weight polyolefins such as polyethylene, polypropylene and polybutene, silicones, fatty acid amides such as oleamide, erucamide, amide ricinoleate and amide stearate, vegetable waxes such as carnauba wax, rice wax, candelilla wax, Japan wax and jojoba oil, animal waxes such as beeswax, mineral/petroleum waxes such as montan wax, ozocerite, ceresin, paraffin wax, microcrystalline wax and Fischer-Tropsch wax, and modified materials thereof are disclosed.
However, when the dispersibility of the release agent added is lowered, the toner images melted during fixing are prone to have a dull color. This also decreases the pigment dispersibility, and thus the color development property of the toner becomes insufficient. In the subsequent process, when resin particles further adhere to the surfaces of aggregated particles, the adhesion of the resin particles is unstable due to the low dispersibility of the release agent or the like. Moreover, the release agent that once was aggregated with the resin is liberated into an aqueous medium. Depending on the polarity or the thermal properties such as a melting point, the release agent may have a considerable effect on aggregation of the particles. Further, a specified wax is added in a large amount to achieve the oilless fixing.
When particles are formed by an aggregation reaction in the medium containing at least a certain amount of wax, the particle size increases with heat treatment time. Therefore, it is difficult to produce small particles having a narrow particle size distribution.
The use of a release agent may achieve the oiless fixing, reduce fog during development, and improve the transfer efficiency. However, such a release agent prevents uniform mixing and aggregation of the resin particles and the pigment particles in the aqueous medium during manufacture. Thus, the release agent is not aggregated but suspended in the aqueous medium, and the aggregated and fused particles are likely to be coarser due to the effect of the release agent.
Patent Document 3 discloses a toner that includes particles formed by polymerization and a coating layer of fine particles that is formed on the surface of the individual particles by emulsion polymerization. A water-soluble inorganic salt may be added, or the pH of the solution may be changed to form the coating layer of fine particles on the surface of the individual particles.
Patent Document 4 discloses a method for producing a toner including the following steps: preparing an aggregated particle dispersion by forming aggregated particles in a dispersion in which at least resin particles are dispersed; adding a resin particle dispersion in which resin particles are dispersed to the aggregated particle dispersion and mixing them so that the resin particles adhere to the aggregated particles to form adhesive particles; and heating and fusing the adhesive particles. In this method, the resin particle dispersion may be added either gradually and continuously or in two or more separate stages. It is described that the addition of the resin particles (additional particles) can suppress the generation of small particles, provide a sharp particle size distribution, and improve the charging performance.
Patent Document 5 discloses a toner that includes a surface-active agent in an amount of 3 wt % or less in the particulate toner and an inorganic metal salt (e.g., zinc chloride) having an electric charge having a valence of two or more in an amount of 1 wt % or less at 10 ppm or more. The toner is formed by ionic cross-linking so as to improve the resistance to moisture absorption. Moreover, the toner is produced by mixing a resin particle dispersion and a colorant particle dispersion, adjusting an agglomerate dispersion with an inorganic metal salt, and heating the agglomerate dispersion at temperatures not less than the glass transition point of the resin so that the agglomerate is fused. It is described that the toner can have not only a small particle size and a sharp particle size distribution, but also excellent chargeability, resistance to environmental dependence, cleaning properties, and transferability.
Patent Document 6 discloses toner particles having a resin layer (shell) formed by fusing resin particles with the surfaces of colored particles (core particles) by a salting-out/fusion method. The colored particles contain a resin and a colorant. After the salting-out/fusion process of forming the colored particles, a resin particle dispersion is added to the colored particle dispersion, and then is maintained at temperatures not less than the glass transition point. It is described that since the amount of the colorant present on the particle surface is small, even if the toner is used for image formation under high humidity environment over a long period of time, it can exhibit the effects of suppressing image density fluctuations, fog, and color changes caused by variations in the charging and developing properties of the toner.
Patent Document 7 discloses a toner for electrostatic charge image development that includes toner particles containing at least a resin and a colorant. The individual toner particles have a core containing a resin A and at least one layer of shell containing a resin B. The core is covered with the shell. The outermost layer of the shell has a thickness of 50 nm to 500 nm. It is described that the toner can exhibit excellent offset resistance and good storage property.
Patent Document 1: JP 10(1998)-198070 A
Patent Document 2: JP 10(1998)-301332 A
Patent Document 3: JP 57 (1982)-045558 A
Patent Document 4: JP 10(1998)-073955 A
Patent Document 5: JP 11(1999)-311877 A
Patent Document 6: JP 2002-116574 A
Patent Document 7: JP 2004-191618 A
It is a first object of the present invention to provide a toner that can have a small particle size and a sharp particle size distribution without requiring a classification process. It is a second object of the present invention to perform oilless fixing (no oil is applied to a fixing roller) by using a release agent such as wax in the toner while achieving low-temperature fixability, high-temperature offset resistance, separability of paper from the fixing roller or the like, and storage stability at high temperatures. It is a third object of the present invention to provide a toner that can have a long life and high resistance to deterioration caused by spent, even if the toner as used includes a release agent such as wax. It is a fourth object of the present invention to provide a toner that can suppress transfer voids or scattering during transfer and ensure high transfer efficiency. A toner of the present invention is produced by mixing in an aqueous medium at least a first resin particle dispersion in which first resin particles are dispersed, a colorant particle dispersion in which colorant particles are dispersed, and a wax particle dispersion in which wax particles are dispersed, aggregating the particles to form core particles, adding a second resin particle dispersion in which second resin particles are dispersed to a core particle dispersion including the core particles, and fusing the second resin particles with the core particles by mixing and heating. The second resin particle dispersion is added after adjusting the pH value in the range of HS+2 to HS−5, where HS represents the pH value of the core particle dispersion in which the core particles are dispersed, so that toner particles have a volume-average particle size of 3 to 7 μm, the content of the toner particles having a particle size of 2.52 to 4 μm in a number distribution is 10 to 75% by number, the toner particles having a particle size of 4 to 6.06 μm in a volume distribution is 25 to 75% by volume, and the toner particles having a particle size of not less than 8 μm in the volume distribution is not more than 5% by volume.
A method for producing a toner of the present invention includes the following: mixing in an aqueous medium at least a first resin particle dispersion in which first resin particles are dispersed, a colorant particle dispersion in which colorant particles are dispersed, and a wax particle dispersion in which wax particles are dispersed; aggregating the particles to form core particles; adding a second resin particle dispersion in which second resin particles are dispersed to a core particle dispersion including the core particles; and fusing the second resin particles with the core particles by mixing and heating. The second resin particle dispersion is added after adjusting the pH value in the range of HS+2 to HS−5, where HS represents the pH value of the core particle dispersion in which the core particles are dispersed.
In the present invention, the core particles are obtained by aggregating the first resin particles and the colorant particles in an aqueous medium, and then the second resin particles are fused with the core particles to form toner base particles. When the second resin particles are added, the pH of the second resin particle dispersion is adjusted within a predetermined range, thereby suppressing the presence of suspended resin particles that are not fused with the core particles and preventing the toner base particles from being coarser. Thus, the toner base particles having a small particle size and a sharp particle size distribution can be produced without requiring a classification process. Moreover, since the pH of the second resin particle dispersion is adjusted within a predetermined range, the adhesion and fusion between the core particles can be adjusted, so that the shape of the toner base particles can be controlled while the second resin particles are added.
Moreover, it is possible not only to improve the low-temperature fixability, the glossiness, and the high-temperature offset resistance, but also to maintain the storage stability.
The toner of the present invention can have high resistance to deterioration caused by spent on a carrier.
In a tandem color process, a plurality of image forming stations, each of which includes a photoconductive member and a developing unit, are provided, and the transfer process is performed by successively transferring each color of toner to a transfer member. The use of the toner of the present invention can suppress transfer voids or reverse transfer and ensure high transfer efficiency.
The toner of the present invention makes it possible to form color images with high quality and high reliability without causing any scattering or fog.
Hereinafter, a method for producing a toner will be described.
(1) Polymerization Process
A resin particle dispersion is prepared by forming resin particles of a homopolymer or copolymer (vinyl resin) of vinyl monomers by emulsion or seed polymerization of the vinyl monomers in a surface-active agent and dispersing the resin particles in the surface-active agent. Any known dispersing devices such as a high-speed rotating emulsifier, a high-pressure emulsifier, a colloid-type emulsifier, and a ball mill, a sand mill, and Dyno mill that use a medium can be used.
When the resin particles are made of resin other than the homopolymer or copolymer of the vinyl monomers, a resin particle dispersion may be prepared in the following manner. If the resin dissolves in an oil solvent that has a relatively low water solubility, a solution is obtained by mixing the resin with the oil solvent. The solution is blended with a surface-active agent or polyelectrolyte, and then is dispersed in water to produce a fine particle dispersion by using a dispersing device such as a homogenizer. Subsequently, the oil solvent is evaporated by heating or under reduced pressure. Thus, the resin particles made of resin other than the vinyl resin are dispersed in the surface-active agent.
Examples of a polymerization initiator include an azo- or diazo-based initiator such as 2,2′-azobis-(2,4-dimethylvaleronitrile), 2,2′-azobisisobutyronitrile, 1,1′-azobis(cyclohexane-1-carbonitrile), 2,2′-azobis-4-methoxy-2,4-dimethylvaleronitrile, or azobisisobutyronitrile, persulfate such as potassium persulfate or ammonium persulfate, an azo compound such as 4,4′-azobis-4-cyanovaleric acid and its salt or 2,2′-azobis(2-amidinopropane) and its salt, and a peroxide compound.
A colorant particle dispersion is prepared by adding colorant particles to water that includes a surface-active agent and dispersing the colorant particles using the above dispersing device.
A wax particle dispersion is prepared by adding wax particles to water that includes a surface-active agent and dispersing the wax particles using an appropriate dispersing device.
The toner is required to achieve fixing at lower temperatures, high-temperature offset resistance in the oilless fixing, releasability, high transmittance of color images, and storage stability at certain high temperatures. These requirements should be satisfied at the same time.
In the toner of the present invention, at least the first resin particle dispersion in which the first resin particles are dispersed, the colorant particle dispersion in which the colorant particles are dispersed, and the wax particle dispersion in which the wax particles are dispersed are mixed in an aqueous medium, and then aggregated to form core particles. Subsequently, the second resin particle dispersion in which the second resin particles are dispersed is added to the core particle dispersion including the core particles, and the resultant dispersion is mixed and heat-treated at temperatures not less than the glass transition point of the second resin particles so that the second resin particles are fused with the core particles. When the second resin particle dispersion is added to the core particle dispersion, the pH of the second resin particle dispersion is adjusted in the range of HS+2 to HS−5, where HS represents the pH value of the core particle dispersion in which the core particles are dispersed.
This configuration suppresses the generation of suspended particles of the second resin particles, so that the second resin particles can adhere uniformly to the surface of the individual core particles. The adhesion of the second resin particles to the core particles can be performed quickly, which makes the fusion time shorter. Thus, the productivity can be improved. Moreover, when the second resin particles are fused with the core particles, the particles can be prevented from being coarser rapidly, and therefore can have a small particle size and a sharp particle size distribution.
The addition of the second resin particle dispersion with a pH value away from that of the core particle dispersion can disturb the pH balance of the liquid suddenly. As a result, there are some cases where the second resin particles do not adhere to the core particles, or the particles produced become coarser due to secondary aggregation of the core particles. To suppress such phenomena, it is effective to adjust the pH of the second resin particle dispersion.
If the pH is more than HS+2, the particles become coarser and the particle size distribution tends to be broader. If the pH is less than HS−5, the adhesion of the second resin particles to the core particles does not proceed, and the process takes a long time. Moreover, the second resin particles continue to be suspended in the aqueous medium, and the liquid is likely to remain white and cloudy.
In the toner of the present invention, when the second resin particle dispersion is added to the core particle dispersion with its pH value being adjusted in the range of HS+2 to HS−1, the occurrence of secondary aggregation of the core particles can be controlled, and the shape of the toner base particles (end product) also can be controlled during the addition of the second resin particles. In other words, the pH of the second resin particle dispersion is adjusted closer to or higher than the pH of the core particle dispersion, thereby allowing secondary aggregation of the core particles to occur partially while the second resin particles are fused with the core particles. Thus, the particle shape can be controlled from spherical particles to potato-shaped particles.
If the pH is more than HS+2, the particles become coarser rapidly and the particle size distribution tends to be broader. If the pH is less than HS−1, the secondary aggregation of the core particles does not proceed, and the particles remain spherical in shape. Thus, it is difficult to control the particle shape. There is a strong tendency to determine the shape of the toner by its compatibility with the development, transfer, and cleaning processes. Therefore, when the importance of the cleaning properties of a conductive member or a transfer belt is stressed, a wider margin for cleaning can be ensured with the potato-shaped particles than the spherical particles of the toner. When the importance of the transfer properties is stressed, the shape of the toner is close to a sphere so as to improve the transfer efficiency.
The second resin particle dispersion may be added at the time the core particles reach a predetermined particle size. The addition can be performed by dropping the second resin particle dispersion either collectively or successively. In this case, the successive dropping is suitable. The drop rate is preferably 1 to 1000 g/min. If the drop rate is lower than 1 g/min, the particle size distribution tends to be broader. If the drop rate is higher than 1000 g/min, the particles are likely to be coarser.
In the toner of the present invention, it is also preferable that the pH value of the second resin particle dispersion to be added to the core particle dispersion is adjusted in the range of 3.5 to 10.5 regardless of the pH value of the core particle dispersion in which the core particles are dispersed. If the pH of the second resin particle dispersion is less than 3.5, the adhesion of the second resin particles to the core particles does not proceed, the second resin particles continue to be suspended in the aqueous medium, and thus the liquid remains white and cloudy. If the pH is more than 10.5, the particles produced are likely to be coarser rapidly.
To improve the durability, storage stability, and high-temperature offset resistance of the toner, the thickness of a resin layer formed by the fusion of the second resin particles is preferably 0.5 μm to 2 μm. If the thickness is less than 0.5 μm, the effects of the storage stability and the high-temperature offset resistance cannot be obtained. If the thickness is more than 2 μm, the low-temperature fixability is impaired.
In the configuration of the toner of the present invention, it is also preferable that the pH of the aqueous medium further is adjusted in the range of 3.2 to 6.8 after the second resin particles adhere to the surface of the individual core particles, and then the aqueous medium is heat-treated at temperatures not less than the glass transition point of the second resin particles for 0.5 to 5 hours. This further can improve the surface smoothness of the particles while suppressing secondary aggregation of the core particles to which the second resin particles have adhered.
In the configuration of the toner of the present invention, the core particles may be produced preferably in the following manner. The first resin particle dispersion in which the first resin particles are dispersed, the colorant particle dispersion in which the colorant particles are dispersed, and the wax particle dispersion in which the wax particles are dispersed are mixed in an aqueous medium. Then, the pH of the aqueous medium is adjusted under predetermined conditions, and a water-soluble inorganic salt is added to the mixed dispersion. Subsequently, the aqueous medium is heated at temperatures not less than the glass transition point (Tg) of the first resin particles and/or the melting point of the wax so that the first resin particles, the colorant particles, and the wax particles are aggregated to form core particles, at least part of which is melted.
When persulfate (e.g., potassium persulfate) is used as a polymerization initiator in the emulsion polymerization of the resin to prepare a resin particle dispersion, the residue may be decomposed by heat applied during the aggregation process and may change (reduce) the pH of the mixed dispersion. Therefore, it is preferable that a heat treatment is performed at temperatures not less than a predetermined temperature (preferably 80° C. or more for sufficient decomposition of the residue) for a predetermined time (preferably about 1 to 5 hours) after the emulsion polymerization. The pH is preferably 4 or less, and more preferably 1.8 or less.
A water-soluble inorganic salt is added to the mixed dispersion, and then is heated at temperatures not less than the glass transition point (Tg) of the first resin particles and/or the melting point of the wax, thereby forming toner base particles with a predetermined particle size. The pH of the mixed dispersion is adjusted preferably in the range of 9.5 to 12.2 before adding the water-soluble inorganic salt and heating. In this case, 1N NaOH can be used for the pH adjustment. If the pH is less than 9.5, the particles produced become coarser. If the pH is more than 12.2, the amount of liberated wax is increased, and it is difficult to incorporate the wax uniformly into the resin.
After the pH adjustment, the water-soluble inorganic salt is added, and the mixed dispersion is heat-treated so that the first resin particles, the colorant particles, and the wax particles are aggregated to form core particles having a predetermined volume-average particle size, and at least part of the core particles is melted. The pH of the dispersion at the time of forming the core particles with the predetermined volume-average particle size is maintained in the range of 7.0 to 9.5. This can reduce the liberation of the wax and thus allows the core particles to incorporate the wax and have a narrow particle size distribution. The amount of NaOH added, the type or amount of aggregating agent, the pH values of the emulsion-polymerized resin dispersion, the colorant dispersion and the wax dispersion, a heating temperature, or time may be selected appropriately. If the pH of the dispersion is less than 7.0 at the time of forming the core particles, the core particles become coarser. If the pH of the dispersion is more than 9.5, the amount of liberated wax is increased due to poor aggregation.
In the process of forming the core particles for the toner of the present invention, it is preferable that the main component of the surface-active agent used for each of the first resin particle dispersion, the colorant particle dispersion, and the wax particle dispersion is a nonionic surface-active agent.
Moreover, in the surface-active agent used for each of the colorant particle dispersion and the wax particle dispersion, the nonionic surface-active agent is preferably 50 to 100 wt %, and more preferably 60 to 100 wt %, of the total surface-active agent.
This configuration eliminates the presence of colorant or wax particles that are not aggregated but suspended in the aqueous medium, and thus can form the core particles having a smaller particle size and a uniform, narrow and sharp particle size distribution. Moreover, the numbers of suspended second resin particles are reduced, and the second resin particles can be fused uniformly with the surface of the individual core particles, providing a sharp particle size distribution.
The surface-active agent used for the first resin particle dispersion may be a mixture of a nonionic surface-active agent and an ionic surface-active agent, and the nonionic surface-active agent is preferably 60 to 95 wt % of the total surface-active agent. If the nonionic surface-active agent is less than 60 wt %, stable core particles cannot be produced. If the nonionic surface-active agent is more than 95 wt %, the dispersion of the resin particles is not stable.
It is also preferable that the surface-active agent used for the first resin particle dispersion is a mixture of a nonionic surface-active agent and an ionic surface-active agent, and the main component of the surface-active agent used for the wax particle dispersion is only a nonionic surface-active agent.
Moreover, it is preferable that the surface-active agent used for the first resin particle dispersion is a mixture of a nonionic surface-active agent and an ionic surface-active agent, the main component of the surface-active agent used for the colorant particle dispersion is only a nonionic surface-active agent, and the main component of the surface-active agent used for the wax particle dispersion is only a nonionic surface-active agent.
When the mixture of nonionic and ionic surface-active agents is used for the first resin particle dispersion, the nonionic surface-active agent is preferably 60 to 95 wt % of the total surface-active agent. If the nonionic surface-active agent is less than 60 wt %, stable core particles cannot be produced. If the nonionic surface-active agent is more than 95 wt %, the dispersion of the resin particles is not stable.
Further, it is preferable that the main component of the surface-active agent used for the second resin particle dispersion is a nonionic surface-active agent.
The surface-active agent used for the second resin particle dispersion may be a mixture of a nonionic surface-active agent and an ionic surface-active agent, and the nonionic surface-active agent is preferably 50 to 95 wt % of the total surface-active agent. If the nonionic surface-active agent is less than 50 wt %, it is difficult to promote the adhesion of the second resin particles to the core particles. If the nonionic surface-active agent is more than 95 wt %, the dispersion of the resin particles is not stable.
The surface-active agent allows the dispersed particles of the wax and the resin to be hydrated by many water molecules. Therefore, the particles are not likely to adhere to each other. However, when an electrolyte is added, it takes the water molecules away from the hydrated particles. Accordingly, the particles can adhere easily, so that more and more particles join and grow into larger particles. In this case, when an ionic surface-active agent, e.g., an anionic surface-active agent is used for both resin dispersion and wax dispersion, although the core particles are formed, some wax particles repel each other while the water molecules are taken away by the electrolyte. Thus, there may be particles formed by aggregating only the wax particles suspended independently. The presence of such particles that are not involved in the aggregation reaction can cause filming of the toner on a photoconductive member, a reduction in image density during development, and an increase in fog. Moreover, the suspended particles gradually join with the core particles as the aggregation reaction proceeds by heating for a predetermined time. Consequently, the resultant particles become coarser and have a broad particle size distribution.
In the case of the wax particle dispersion using a nonionic surface-active agent, when an electrolyte is added, it takes the water molecules away from the hydrated particles. Accordingly, the particles can adhere easily, so that more and more particles join and grow into larger particles. Since the nonionic surface-active agent is used, the effect of repulsion of the wax particles is small while the water molecules are taken away by the electrolyte. This can suppress the presence of particles formed by aggregating only the wax particles suspended independently. Thus, it is possible to produce particles having a uniform sharp particle size distribution.
The water-soluble inorganic salt may be, e.g., an alkali metal salt or an alkaline-earth metal salt. Examples of the alkali metal include lithium, potassium, and sodium. Examples of the alkaline-earth metal include magnesium, calcium, strontium, and barium. Among these, potassium, sodium, magnesium, calcium, and barium are preferred. The counter ions (the anions constituting a salt) of the above alkali metals or alkaline-earth metals may be, e.g., a chloride ion, bromide ion, iodide ion, carbonate ion, or sulfate ion.
Examples of the organic solvent with infinite solubility in water include methanol, ethanol, 1-propanol, 2-propanol, ethylene glycol, glycerin, and acetone. Among these, alcohols having a carbon number of not more than 3 such as methanol, ethanol, 1-propanol, and 2-propanol are preferred, and 2-propanol is particularly preferred.
The nonionic surface-active agent may be, e.g., a polyethylene glycol-type nonionic surface-active agent or a polyol-type nonionic surface-active agent. Examples of the polyethylene glycol-type nonionic surface-active agent include a higher alcohol ethylene oxide adduct, alkylphenol ethylene oxide adduct, fatty acid ethylene oxide adduct, polyol fatty acid ester ethylene oxide adduct, fatty acid amide ethylene oxide adduct, ethylene oxide adduct of fats and oils, and polypropylene glycol ethylene oxide adduct. Examples of the polyol-type nonionic surface-active agent include fatty acid ester of glycerol, fatty acid ester of pentaerythritol, fatty acid ester of sorbitol and sorbitan, fatty acid ester of cane sugar, polyol alkyl ether, and fatty acid amide of alkanolamines.
In particular, the polyethylene glycol-type nonionic surface-active agent such as a higher alcohol ethylene oxide adduct or alkylphenol ethylene oxide adduct can be used preferably.
Examples of the aqueous medium include water such as distilled water or ion-exchanged water, and alcohols. They can be used individually or in combinations of two or more. The content of the polar surface-active agent need not be defined generally and may be selected appropriately depending on the purposes.
When the nonionic surface-active agent is used with the ionic surface-active agent, the polar surface-active agent may be, e.g., a sulfate-based, sulfonate-based, or phosphate-based anionic surface-active agent or an amine salt-type or quaternary ammonium salt-type cationic surface-active agent.
Specific examples of the anionic surface-active agent include sodium dodecyl benzene sulfonate, sodium dodecyl sulfate, sodium alkyl naphthalene sulfonate, and sodium dialkyl sulfosuccinate.
Specific examples of the cationic surface-active agent include alkyl benzene dimethyl ammonium chloride, alkyl trimethyl ammonium chloride, and distearyl ammonium chloride. They can be used individually or in combinations of two or more.
After the second resin particles are fused with the core particles to form a resin layer, cleaning, liquid-solid separation, and drying processes may be performed as desired to provide toner base particles. The cleaning process preferably involves sufficient substitution cleaning with ion-exchanged water to improve the chargeability. The liquid-solid separation process is not particularly limited, and any known filtration methods such as suction filtration and pressure filtration can be used preferably in view of productivity. The drying process is not particularly limited, and any known drying methods such as flash-jet drying, flow drying, and vibration-type flow drying can be used preferably in view of productivity.
(2-1) Wax
It is preferable that a wax is added to a toner so as to improve the low-temperature fixability the high-temperature offset resistance, or the separability of a transfer medium such as copy paper, on which the molten toner is put during fixing, from a heating roller or the like. Even if only one type of wax is used, it still can be effective.
Examples of suitable waxes include the following:
(a) esters composed of higher alcohol having a carbon number of 16 to 24 and higher fatty acid having a carbon number of 16 to 24 such as stearyl stearate, palmityl palmitate, behenyl behenate or stearyl montanate;
(b) esters composed of higher fatty acid having a carbon number of 16 to 24 and lower monoalcohol such as butyl stearate, isobutyl behenate, propyl montanate or 2-ethylhexyl oleate;
(c) esters composed of higher fatty acid having a carbon number of 16 to 24 and polyalcohol such as montanic acid monoethylene glycol ester, ethylene glycol distearate, glyceride monostearate, glyceride monobehenate, glyceride tripalmitate, pentaerythritol monobehenate, pentaerythritol dilinoleate, pentaerythritol trioleate or pentaerythritol tetrastearate; and
(d) esters composed of higher fatty acid having a carbon number of 16 to 24 and a polyalcohol polymer such as diethylene glycol monobehenate, diethylene glycol dibehenate, dipropylene glycol monostearate, diglyceride distearate, triglyceride tetrastearate, tetraglyceride hexabehenate or decaglyceride decastearate. These waxes can be used individually or in combinations of two or more.
Moreover, meadowfoam oil or its derivative, jojoba oil or its derivative, carnauba wax, Japan wax, beeswax, ozocerite, candelilla wax, ceresin wax, or rice wax can be used preferably.
A derivative of hydroxystearic acid, glycerin fatty acid ester, glycol fatty acid ester, or sorbitan fatty acid ester also can be used preferably.
A fatty acid hydrocarbon wax such as a low molecular weight polypropylene wax, low molecular weight polyethylene wax, polypropylene-polyethylene copolymer wax, microcrystalline wax, paraffin wax or Fischer-Tropsch wax also can be used preferably.
The melting point of the wax is preferably 50° C. to 120° C., more preferably 60° C. to 110° C., and further preferably 65° C. to 100° C. If the melting point is lower than 50° C., the storage stability is degraded. If it is higher than 120° C., the low-temperature fixability and the color glossiness cannot be improved. The aggregation of the wax is reduced, and the numbers of liberated particles are likely to be increased in the aqueous medium.
The amount of the wax added is preferably 5 to 30 parts by weight, more preferably 8 to 25 parts by weight, and further preferably 10 to 20 parts by weight per 100 parts by weight of the binder resin. If the amount is less than 5 parts by weight, the effects of the low-temperature fixability, the high-temperature offset resistance, and the separability of paper cannot be obtained. If the amount is more than 30 parts by weight, it is difficult to control small particles.
The wax should be incorporated uniformly into the resin so as not to be liberated or suspended during mixing and aggregation. This may be affected by the particle size distribution, composition, and melting property of the wax.
The wax particle dispersion may be prepared in such a manner that wax is mixed in an aqueous medium (e.g., ion-exchanged water) including the surface-active agent, and then is heated, melted, and dispersed.
In this case, the wax may be emulsified and dispersed so that the particle size is 20 to 200 nm for 16% diameter (PR16), 40 to 300 nm for 50% diameter (PR50), not more than 400 nm for 84% diameter (PR84), and PR84/PR16 is 1.2 to 2.0 in a cumulative volume particle size distribution obtained by accumulation from the smaller particle diameter side. It is preferable that the ratio of particles having a diameter not greater than 200 nm is 65 vol % or more, and the ratio of particles having a diameter greater than 500 nm is 10 vol % or less.
Preferably, the particle size may be 20 to 100 nm for 16% diameter (PR16), 40 to 160 nm for 50% diameter (PR50), not more than 260 nm for 84% diameter (PR84), and PR84/PR16 is 1.2 to 1.8. It is preferable that the ratio of particles having a diameter not greater than 150 nm is 65 vol % or more, and the ratio of particles having a diameter greater than 400 nm is 10 vol % or less.
More preferably, the particle size may be 20 to 60 nm for 16% diameter (PRIG), 40 to 120 nm for 50% diameter (PR50), not more than 220 nm for 84% diameter (PR84), and PR84/PR16 is 1.2 to 1.8. It is preferable that the ratio of particles having a diameter not greater than 130 nm is 65 vol % or more, and the ratio of particles having a diameter greater than 300 nm is 10 vol % or less.
When the resin particle dispersion, the colorant particle dispersion, and the wax particle dispersion are mixed and aggregated to form core particles, the wax with a particle size of 40 to 300 nm for 50% diameter (PR50) is dispersed finely and thus incorporated easily into the resin particles. Therefore, it is possible to prevent aggregation of the wax particles themselves that are not aggregated with the resin particles and the colorant particles, to achieve uniform dispersion, and to eliminate the suspended particles in the aqueous medium.
Moreover, when the core particles are heated and melted in the aqueous medium, the molten wax is covered with the molten resin particles due to surface tension, so that the wax can be incorporated easily into the resin particles.
If the particle size is more than 200 nm for PR16, more than 300 nm for PR50, and more than 400 nm for PR84, PR84/PR16 is more than 2.0, the ratio of particles having a diameter not greater than 200 nm is less than 65 vol %, or the ratio of particles having a diameter greater than 500 nm is more than 10 vol %, the wax particles are not incorporated easily into the resin particles and thus are prone to aggregation by themselves. Therefore, a large number of particles that are not incorporated into the resin particles are likely to be suspended in the aqueous medium. When the core particles are heated and melted in the aqueous medium, the molten wax is not covered with the molten resin particles, so that the wax cannot be incorporated easily into the resin particles. Moreover, the amount of wax that is exposed on the surfaces of the core particles and liberated therefrom is increased while further resin particles are fused. This may increase filming of the toner on a photoconductive member or spent of the toner on a carrier, reduce the handling property of the toner in a developing unit, and cause a developing memory.
If the particle size is less than 20 nm for PR16 and less than 40 nm for PR50, and PR84/PR16 is less than 1.2, it is difficult to maintain the dispersion state, and reaggregation of the wax occurs during the time it is allowed to stand, so that the standing stability of the particle size distribution can be degraded. Moreover, the load and heat generation are increased while the particles are dispersed, thus reducing productivity.
When the particle size for 50% diameter (PR50) of the wax dispersed in the wax particle dispersion is smaller than the particle size for 50% diameter (PR50) of the resin particles in forming the core particles, the wax can be incorporated easily into the resin particles. Therefore, it is possible to prevent aggregation of the wax particles themselves that are not aggregated with the resin particles and the colorant particles, to achieve uniform dispersion, and to eliminate the suspended particles in the aqueous medium. Moreover, when the core particles are heated and melted in the aqueous medium, the molten wax is covered with the molten resin particles due to surface tension, so that the wax can be incorporated easily into the resin particles. It is more preferable that the particle size for 50% diameter (PR50) of the wax is at least 20% smaller than that of the resin particles.
The wax particles can be dispersed finely in the following manner. A wax melt in which the wax is melted at a concentration of not more than 40 wt % is emulsified and dispersed into a medium that includes a surface-active agent and is maintained at temperatures not less than the melting point of the wax by utilizing the effect of a strong shearing force generated when a rotating body rotates at high speed relative to a fixed body with a predetermined gap between them.
As shown in
As shown in
In this manner, it is possible to form a narrower and sharper particle size distribution of the fine particles than using a dispersing device such as a homogenizer. It is also possible to maintain a stable dispersion state without causing any reaggregation of the fine particles in the dispersion even when left standing for a long time. Thus, the standing stability of the particle size distribution can be improved.
When the wax has a high melting point, it may be heated under high pressure to form a melt. Alternatively, the wax may be dissolved in an oil solvent. This solution is blended with a surface-active agent or polyelectrolyte and dispersed in water to make a fine particle dispersion by using either of the dispersing devices as shown in
The particle size can be measured, e.g., by using a laser diffraction particle size analyzer LA920 (manufactured by Horiba, Ltd.) or SALD2100 (manufactured by Shimadzu Corporation).
(2-2) Wax
It is preferable that a plurality of types of waxes are added so as to improve the low-temperature fixability, the high-temperature offset resistance, or the separability of a transfer medium such as copy paper, on which the molten toner is put during fixing, from a heating roller or the like, to increase tolerances for the opposing fixing characteristics of low-temperature fixability, high-temperature offset resistance and storage stability, and also to enhance the functionality.
The wax particle dispersion may be prepared in such a manner that wax is mixed in an aqueous medium (e.g., ion-exchanged water) including the surface-active agent, and then is heated, melted, and dispersed.
As a first preferred configuration, the wax may include at least a first wax and a second wax, the endothermic peak temperature (melting point: Tm1 (° C.)) of the first wax based on a DSC method is 50° C. to 90° C., and the endothermic peak temperature (melting point: Tm2 (° C.)) of the second wax based on the DSC method is 5° C. to 50° C. higher than Tm1. The low melting point wax is used to provide the low-temperature fixability, and the high melting point wax is used to achieve the high-temperature offset resistance and the separability of paper.
In the first preferred configuration of the wax, the melting point Tm1 of the first wax is preferably 55° C. to 85° C., more preferably 60° C. to 85° C., and further preferably 65° C. to 75° C. If Tm1 is lower than 50° C., the storage stability is degraded. If Tm1 is higher than 90° C., the low-temperature fixability and the color glossiness cannot be improved. Moreover, the melting point Tm2 of the second wax is preferably at least 5° C. higher than Tm1 of the first wax. Thus, the functions of the waxes can be separated efficiently, so that the low-temperature fixability, the high-temperature offset resistance, and the separability of paper can be ensured together. If the temperature difference is less than 5° C., it is difficult to exhibit the effects of the low-temperature fixability, the high-temperature offset resistance, and the separability of paper. If the temperature difference is more than 50° C., the first and second waxes are phase-separated and not incorporated uniformly into the toner particles.
The melting point Tm2 of the second wax is preferably 80° C. to 120° C., more preferably 85° C. to 100° C., and further preferably 90° C. to 100° C. If Tm2 is lower than 80° C., the high-temperature offset resistance and the separability of paper are weakened. If Tm2 is higher than 120° C., the aggregation of the wax is reduced and the numbers of liberated particles are increased in the aqueous medium.
In the first preferred configuration of the wax, the waxes with different melting points are aggregated with the resin and the colorant in the aqueous medium to form toner particles. In this case, when a dispersion obtained by emulsifying and dispersing the first wax and the second wax separately is mixed with the resin particle dispersion and the colorant particle dispersion, and then this mixed dispersion is heated and aggregated, some wax is not incorporated into the molten core particles (toner particles) due to a difference in melting rate between the waxes, and suspended particles are present in the aqueous medium. Thus, the aggregation of the core particles does not proceed, and the particle size distribution tends to be broader. Therefore, it may be difficult to incorporate the wax uniformly into the toner, and to form particles having a small particle size and a narrow particle size distribution. Moreover, the problem of a rapid change of the particles produced to coarse particles when the second resin is fused with the core particles (to form a shell) also cannot be solved satisfactorily.
Accordingly, it is preferable that the wax particle dispersion is produced by mixing, emulsifying, and dispersing the first wax and the second wax together. In this method, the first wax and the second wax may be mixed at a predetermined mixing ratio, and then heated, emulsified, and dispersed in an emulsifying and dispersing device. The first wax and the second wax may be put in the device either separately or simultaneously. However, it is preferable that the wax particle dispersion thus produced includes the first wax and the second wax in the mixed state.
As a second preferred configuration, the wax may include at least a first wax and a second wax, the first wax may include at least one ester wax selected from higher alcohol having a carbon number of 16 to 24 and higher fatty acid having a carbon number of 16 to 24, and the second wax may include an aliphatic hydrocarbon wax.
As a third preferred configuration, the wax may include at least a first wax and a second wax, the first wax may include a wax having an iodine value of not more than 25 and a saponification value of 30 to 300, and the second wax may include an aliphatic hydrocarbon wax.
In the second and third preferred configurations of the wax, the endothermic peak temperature (melting point: Tm1 (° C.)) of the first wax based on the DSC method is 50° C. to 90° C., preferably 55° C. to 85° C., more preferably 600° to 85° C., and further preferably 650° to 75° C. If Tm1 is lower than 50° C., the storage stability and the heat resistance of the toner are degraded. If Tm1 is higher than 90° C., the aggregation of the wax is reduced, and the numbers of liberated particles are increased in the aqueous medium. Moreover, the low-temperature fixability and the glossiness cannot be improved.
In the second and third preferred configurations of the wax, the endothermic peak temperature (melting point: Tm2 (° C.)) of the second wax based on the DSC method is 80° C. to 120° C., preferably 85° C. to 100° C., and more preferably 90° C. to 100° C. If Tm2 is lower than 80° C., the storage stability is degraded, and the high-temperature offset resistance and the separability of paper are weakened. If Tm2 is higher than 120° C., the aggregation of the wax is reduced, and the numbers of liberated particles are increased in the aqueous medium. Moreover, the low-temperature fixability and the color transmittance are impaired.
In the second or third preferred configuration of the wax, when the resin, the colorant, and the aliphatic hydrocarbon wax are mixed to form core particles in an aqueous medium, the aliphatic hydrocarbon wax is unlikely to be aggregated with the resin because of its conformability with the resin. Therefore, some wax is not incorporated into the molten core particles, and suspended particles are present in the aqueous medium. Such presence of the suspended particles may hinder the progress of aggregation and make the particle size distribution broader.
However, if the temperature or time of the heat treatment is changed to reduce the suspended particles or to prevent a broad particle size distribution, the particle size is increased. Moreover, when the second resin particles are added further to form a shell, the core particles become coarser rapidly.
By using the wax that includes the first wax including a specified wax and the second wax including a specified aliphatic hydrocarbon wax, it is possible to suppress the presence of suspended particles that do not incorporate the aliphatic hydrocarbon wax and to prevent the particle size distribution of the core particles from being broader. Moreover, when the second resin particles are added to form a shell, it is also possible to reduce a phenomenon in which the core particles become coarser rapidly.
In the process of heating and aggregation, it is assumed that the first wax continues to be compatibilized with the resin, which promotes aggregation of the aliphatic hydrocarbon wax and the resin, and therefore the wax is incorporated uniformly, and the presence of suspended particles can be suppressed. When the first wax is partially compatibilized with the resin, it tends to improve the low-temperature fixability further. The aliphatic hydrocarbon wax is not compatibilized with the resin, and thus can have the effects of improving the high-temperature offset resistance and the separability of paper. In other words, the first wax may function as both a dispersion assistant for emulsifying and dispersing the aliphatic hydrocarbon wax and a low-temperature fixing assistant.
In the second or third preferred configuration of the wax, as described in the first preferred configuration, it is preferable that the wax particle dispersion is produced by mixing, emulsifying, and dispersing the first wax and the second wax together. This can suppress the presence of suspended particles that do not incorporate the wax and reduce a phenomenon in which the core particles become coarser rapidly in forming a shell. Thus, it is possible to incorporate the wax uniformly into the toner, and to form particles having a smaller particle size and a narrower particle size distribution. In the first, second or third preferred configuration of the wax, it is preferable that FT2/ES1 is 0.2 to 10, and more preferably 1 to 9 where ES1 and FT2 are weight ratios of the first wax and the second wax to 100 parts by weight of the wax in the wax particle dispersion, respectively. If FT2/ES1 is less than 0.2 (i.e., the weight ratio of the first wax is too large), the effect of the high-temperature offset resistance cannot be obtained, and the storage stability is degraded. If FT2/IS1 is more than 10 (i.e., the weight ratio of the second wax is too large), the low-temperature fixing cannot be achieved, and the core particles are likely to be coarser. Moreover, FT2 of 50 wt % or more is a well-balanced ratio at which the low-temperature fixability, the high-temperature storage stability, and the high-temperature offset resistance can be achieved.
In the first, second or third preferred configuration of the wax, although the dispersion stability is improved by treating the wax, particularly the aliphatic hydrocarbon wax with an anionic surface-active agent, when the particles are aggregated to form core particles, the core particle become coarser, and it may be difficult to obtain particles having a sharp particle size distribution.
Therefore, the wax particle dispersion is produced preferably by mixing, emulsifying, and dispersing the first wax and the second wax with a surface-active agent that includes a nonionic surface-active agent as the main component. When the first wax and the second wax are mixed and dispersed to form an emulsion dispersion by using the surface-active agent that includes a nonionic surface-active agent as the main component, aggregation of the wax particles themselves can be suppressed, and the dispersion stability can be improved. Then, this wax particle dispersion is mixed with the resin particle dispersion and the colorant particle dispersion, so that the core particles are formed. In this manner, the wax particles are not liberated, and the core particles can have a small particle size and a narrow sharp particle size distribution.
In the first, second or third preferred configuration of the wax, the total amount of the wax added is preferably 5 to 30 parts by weight, more preferably 8 to 25 parts by weight, and further preferably 10 to 20 parts by weight per 100 parts by weight of the binder resin. If the amount is less than 5 parts by weight, the effects of the low-temperature fixability, the high-temperature offset resistance, and the separability of paper cannot be obtained. If the amount is more than 30 parts by weight, it is difficult to control small particles.
As a preferred configuration of the first wax, the first wax may include at least one type of ester that includes at least one of higher alcohol having a carbon number of 16 to 24 and higher fatty acid having a carbon number of 16 to 24. The use of this wax can suppress the presence of suspended particles that do not incorporate the aliphatic hydrocarbon wax and prevent the particle size distribution of the core particles from being broader. Moreover, when the second resin particles are added to form a shell, it is also possible to reduce a phenomenon in which the core particles become coarser rapidly. Further, the low-temperature fixing is allowed to proceed. By using the first wax with the second wax, it is possible to achieve the high-temperature offset resistance and the separability of paper, to prevent an increase in the particle size, and to produce toner base particles having a small particle size and a narrow particle size distribution.
Examples of the alcohol components include methyl, ethyl, propyl, or butyl monoalcohol, glycols such as ethylene glycol or propylene glycol or polymers thereof, triols such as glycerin or polymers thereof, and polyalcohol such as pentaerythritol, sorbitan, and cholesterol. When these alcohol components are polyalcohol, the higher fatty acid may be either monosubstituted or polysubstituted. Specific examples include the following:
(a) esters composed of higher alcohol having a carbon number of 16 to 24 and higher fatty acid having a carbon number of 16 to 24 such as stearyl stearate, palmityl palmitate, behenyl behenate or stearyl montanate;
(b) esters composed of higher fatty acid having a carbon number of 16 to 24 and lower monoalcohol such as butyl stearate, isobutyl behenate, propyl montanate or 2-ethylhexyl oleate;
(c) esters composed of higher fatty acid having a carbon number of 16 to 24 and polyalcohol such as montanic acid monoethylene glycol ester, ethylene glycol distearate, glyceride monostearate, glyceride monobehenate, glyceride tripalmitate, pentaerythritol monobehenate, pentaerythritol dilinoleate, pentaerythritol trioleate or pentaerythritol tetrastearate; and
(d) esters composed of higher fatty acid having a carbon number of 16 to 24 and a polyalcohol polymer such as diethylene glycol monobehenate, diethylene glycol dibehenate, dipropylene glycol monostearate, diglyceride distearate, triglyceride tetrastearate, tetraglyceride hexabehenate or decaglyceride decastearate. These waxes can be used individually or in combinations of two or more.
If the carbon number of the alcohol component and/or the acid component is less than 16, the wax is not likely to function as a dispersion assistant. If it is more than 24, the wax is not likely to function as a low-temperature fixing assistant.
As a preferred configuration of the first wax, the first wax may include a wax having an iodine value of not more than 25 and a saponification value of 30 to 300. By using the first wax with the second wax, an increase in the particle size can be prevented, thus producing toner base particles having a small particle size and a narrow particle size distribution. When the iodine value is defined, the dispersion stability of the wax can be improved, and the wax, resin, and colorant particles can be formed uniformly into core particles, so that particles having a small size and a narrow particle size distribution can be produced. Preferably, the iodine value is not more than 20 and the saponification value is 30 to 200. More preferably, the iodine value is not more than 10 and the saponification value is 30 to 150. If the iodine value is more than 25, the dispersion stability is too high, and the wax, resin, and colorant particles cannot be formed uniformly into core particles. Thus, the numbers of suspended particles of the wax are likely to be increased, the particles become coarser, and the particle size distribution tends to be broader. The suspended particles may remain in the toner and cause filming of the toner on a photoconductive member or the like. Therefore, the repulsion due to the charging action of the toner cannot be relieved easily during multilayer transfer in the primary transfer process. If the saponification value is less than 30, the presence of unsaponifiable matter and hydrocarbon is increased and makes it difficult to form small uniform core particles. This may result in filming of the toner on a photoconductive member, low chargeability of the toner, and a reduction in chargeability during continuous use. If the saponification value is more than 300, the numbers of suspended solids in the aqueous medium are increased significantly. The repulsion due to the charging action of the toner cannot be relieved easily. Moreover, fog or toner scattering may be increased.
The wax with a predetermined iodine value and a predetermined saponification value preferably has a heating loss of not more than 8 wt % at 220° C. If the heating loss is more than 8 wt %, the glass transition point of the toner becomes low, and the storage stability is degraded. Therefore, such wax adversely affects the development property and allows fog or filming of the toner on a photoconductive member to occur. The particle size distribution of the toner becomes broader.
In the molecular weight characteristics of the wax with a predetermined iodine value and a predetermined saponification value, based on gel permeation chromatography (GPC), it is preferable that the number-average molecular weight is 100 to 5000, the weight-average molecular weight is 200 to 10000, the ratio (weight-average molecular weight/number-average molecular weight) of the weight-average molecular weight to the number-average molecular weight is 1.01 to 8, the ratio (Z-average molecular weight/number-average molecular weight) of the Z-average molecular weight to the number-average molecular weight is 1.02 to 10, and there is at least one molecular weight maximum peak in the range of 5×102 to 1×104. It is more preferable that the number-average molecular weight is 500 to 4500, the weight-average molecular weight is 600 to 9000, the weight-average molecular weight/number-average molecular weight ratio is 1.01 to 7, and the Z-average molecular weight/number-average molecular weight ratio is 1.02 to 9. It is further preferable that the number-average molecular weight is 700 to 4000, the weight-average molecular weight is 800 to 8000, the weight-average molecular weight/number-average molecular weight ratio is 1.01 to 6, and the Z-average molecular weight/number-average molecular weight ratio is 1.02 to 8.
If the number-average molecular weight is less than 100, the weight-average molecular weight is less than 200, or the molecular weight maximum peak is in the range smaller than 5×102, the storage stability is degraded. Moreover, the handling property of the toner in a developing unit is reduced and thus impairs the stability of the toner concentration. The filming of the toner on a photoconductive member may occur. The particle size distribution of the toner becomes broader.
If the number-average molecular weight is more than 5000 the weight-average molecular weight is more than 10000, the weight-average molecular weight/number-average molecular weight ratio is more than 8, the Z-average molecular weight/number-average molecular weight ratio is more than 10, and the molecular weight maximum peak is in the range larger than 1×104, the releasing action is weakened, and the low-temperature fixability is degraded. Moreover, it is difficult to reduce the particle size of the emulsified and dispersed particles of the wax.
It is preferable to use a material having a rate of volume increase of 2 to 30% when the temperature changes by 10° C. above the melting point of the wax with a predetermined iodine value and a predetermined saponification value. Such a material expands rapidly upon changing from solid to liquid, so that when it is melted by heat during fixing, the toner particles adhere to each other more strongly. This further can improve the fixability, the releasability from the fixing roller, and the offset resistance.
Suitable materials for the first wax may be, e.g., meadowfoam oil, carnauba wax, jojoba oil, Japan wax, beeswax, ozocerite, candelilla wax, ceresin wax, rice wax, and derivatives thereof. They can be used individually or in combinations of two or more.
Examples of the meadowfoam oil derivative include meadowfoam oil fatty acid, a metal salt of the meadowfoam oil fatty acid, meadowfoam oil fatty acid ester, hydrogenated meadowfoam oil, and meadowfoam oil triester. These materials can be used to produce an emulsified dispersion having a small particle size and a uniform particle size distribution. Moreover, the materials are effective to improve the low-temperature fixability in the oilless fixing, the life of a developer, and the transfer property. They can be used individually or in combinations of two or more.
The meadowfoam oil fatty acid obtained by saponifying meadowfoam oil preferably includes fatty acid having 4 to 30 carbon atoms. As a metal salt of the meadowfoam oil fatty acid, e.g., metal salts of sodium, potassium, calcium, magnesium, barium, zinc, lead, manganese, iron, nickel, cobalt, aluminum or the like can be used. With these materials, the high-temperature offset resistance can be improved.
Examples of the meadowfoam oil fatty acid ester include methyl, ethyl, butyl, and esters of glycerin, pentaerythritol, polypropylene glycol and trimethylol propane. In particular, e.g., meadowfoam oil fatty acid pentaerythritol monoester, meadowfoam oil fatty acid pentaerythritol triester, or meadowfoam oil fatty acid trimethylol propane ester is preferred. These materials can improve the low-temperature fixability.
The hydrogenated meadowfoam oil can be obtained by adding hydrogen to meadowfoam oil to convert unsaturated bonds to saturated bonds. This material can improve the low-temperature fixability and the glossiness.
Moreover, an isocyanate polymer of meadowfoam oil fatty acid polyol ester, which is obtained by cross-linking a product of the esterification reaction between meadowfoam oil fatty acid and polyhydric alcohol (e.g., glycerin, pentaerythiitol, or trimethylol propane) with isocyanate such as tolylene diisocyanate (TDI) or diphenylmetane-4,4′-diisocyanate (MDI), can be used preferably. This material can suppress spent on a carrier, so that the life of a two-component developer can be made even longer.
Examples of the jojoba oil derivative include jojoba oil fatty acid, a metal salt of the jojoba oil fatty acid, jojoba oil fatty acid ester, hydrogenated jojoba oil, jojoba oil triester, a maleic acid derivative of epoxidized jojoba oil, an isocyanate polymer of jojoba oil fatty acid polyol ester, and halogenated modified jojoba oil. These materials can be used to produce an emulsified dispersion having a small particle size and a uniform particle size distribution. The resin and the wax can be mixed and dispersed uniformly. Moreover, the materials are effective to improve the low-temperature fixability in the oilless fixing, the life of a developer, and the transfer property. They can be used individually or in combinations of two or more.
The jojoba oil fatty acid obtained by saponifying jojoba oil preferably includes fatty acid having 4 to 30 carbon atoms. As a metal salt of the jojoba oil fatty acid, e.g., metal salts of sodium, potassium, calcium, magnesium, barium, zinc, lead, manganese, iron, nickel, cobalt, aluminum or the like can be used. With these materials, the high-temperature offset resistance can be improved.
Examples of the jojoba oil fatty acid ester include methyl, ethyl, butyl, and esters of glycerin, pentaerythritol, polypropylene glycol and trimethylol propane. In particular, e.g., jojoba oil fatty acid pentaerythiritol monoester, jojoba oil fatty acid pentaerythritol triester, or jojoba oil fatty acid trimethylol propane ester is preferred. These materials can improve the low-temperature fixability.
The hydrogenated jojoba oil can be obtained by adding hydrogen to jojoba oil to convert unsaturated bonds to saturated bonds. This material can improve the low-temperature fixability and the glossiness.
Moreover, an isocyanate polymer of jojoba oil fatty acid polyol ester, which is obtained by cross-linking a product of the esterification reaction between jojoba oil fatty acid and polyhydric alcohol (e.g., glycerin, pentaerythritol, or trimethylol propane) with isocyanate such as tolylene diisocyanate (TDI) or diphenylmetane-4,4′-diisocyanate (MDI), can be used preferably. This material can suppress spent on a carrier, so that the life of a two-component developer can be made even longer.
The saponification value is the milligrams of potassium hydroxide (KOH) required to saponify a 1 g sample and corresponds to the sum of an acid value and an ester value. When the saponification value is measured, a sample is saponified with approximately 0.5N potassium hydroxide in an alcohol solution, and then excess potassium hydroxide is titrated with 0.5N hydrochloric acid.
The iodine value may be determined in the following manner. The amount of halogen absorbed by a sample is measured while the halogen acts on the sample. Then, the amount of halogen absorbed is converted to iodine and expressed in grams per 100 g of the sample. The iodine value is grams of iodine absorbed, and the degree of unsaturation of fatty acid in the sample increases with the iodine value. A chloroform or carbon tetrachloride solution is prepared as a sample, and an alcohol solution of iodine and mercuric chloride or a glacial acetic acid solution of iodine chloride is added to the sample. After the sample is allowed to stand, the iodine that remains without undergoing any reaction is titrated with a sodium thiosulfate standard solution, thus calculating the amount of iodine absorbed.
The heating loss may be measured in the following manner. A sample cell is weighed precisely to the first decimal place (W1 mg). Then, 10 to 15 mg of sample is placed in the sample cell and weighed precisely to the first decimal place (W2 mg). This sample cell is set in a differential thermal balance and measured with a weighing sensitivity of 5 mg. After measurement, the weight loss (W3 mg) of the sample at 220° C. is read to the first decimal place using a chart. The measuring device is, e.g., TGD-3000 (manufactured by ULVAC-RICO, Inc.), the rate of temperature rise is 10° C./min, the maximum temperature is 220° C., and the retention time is 1 min. Accordingly, the heating loss can be determined by the following equation.
Heating loss(%)=W3/(W2−W1)×100l
Preferred materials that can be used together or instead of the above wax as the first wax may be, e.g., a derivative of hydroxystearic acid, glycerin fatty acid ester, glycol fatty acid ester, or sorbitan fatty acid ester. They can be used individually or in combinations of two or more. These materials can produce smaller particles that are emulsified and dispersed uniformly. By using the first wax with the second wax, an increase in the particle size can be prevented, thus producing toner base particles having a small particle size and a narrow particle size distribution.
The oilless fixing that provides high glossiness and high transmittance can be achieved at low temperatures. Moreover, the life of a developer can be made longer while achieving the oilless fixing.
Examples of the derivative of hydroxystearic acid include methyl 12-hydroxystearate, butyl 12-hydroxystearate, propylene glycol mono12-hydroxystearate, glycerin mono12-hydroxystearate, and ethylene glycol mono12-hydroxystearate. These materials have the effects of improving the low-temperature fixability and the separability of paper in the oilless fixing and preventing filming of the toner on a photoconductive member.
Examples of the glycerin fatty acid ester include glycerol stearate, glycerol distearate, glycerol tristearate, glycerol monopalmitate, glycerol dipalmitate, glycerol tripalmitate, glycerol behenate, glycerol dibehenate, glycerol tribehenate, glycerol monomyristate, glycerol dimyristate, and glycerol trimyristate. These materials have the effects of relieving cold offset at low temperatures in the oilless fixing and preventing a reduction in the transfer property.
Examples of the glycol fatty acid ester include propylene glycol fatty acid ester such as propylene glycol monopalmitate or propylene glycol monostearate and ethylene glycol fatty acid ester such as ethylene glycol monostearate or ethylene glycol monopalmitate. These materials have the effects of improving the low-temperature fixability and preventing spent on a carrier while increasing the sliding property in development.
Examples of the sorbitan fatty acid ester include sorbitan monopalmitate, sorbitan monostearate, sorbitan tripalmitate, and sorbitan tristearate. Moreover, stearic acid ester of pentaerythritol, mixed esters of adipic acid and stearic acid or oleic acid, and the like are preferred. They can be used individually or in combinations of two or more. These materials have the effects of improving the separability of paper in the oilless fixing and preventing filming of the toner on a photoconductive member.
Preferred examples of the second wax include fatty acid hydrocarbon wax such as low molecular weight polypropylene wax, low molecular weight polyethylene wax, polypropylene-polyethylene copolymer wax, microcrystalline wax, paraffin wax, or Fischer-Tropsch wax.
As the second wax, e.g., a modified wax obtained by the reaction of long chain alkyl alcohol, unsaturated polycarboxylic acid or its anhydride, and synthetic hydrocarbon wax also can be used.
In this modified second wax, it is preferable that the long chain alkyl group has a carbon number of 4 to 30, and the acid value is 10 to 80 mgKOH/g. Moreover, the second wax may be obtained by the reaction of long chain alkylamine, unsaturated polycarboxylic acid or its anhydride, and unsaturated hydrocarbon wax. Alternatively, the second wax may be obtained by the reaction of long chain fluoroalkyl alcohol, unsaturated polycarboxylic acid or its anhydride, and unsaturated hydrocarbon wax. In either case, the long chain alkyl group can promote the releasing action, the ester group can improve the dispersibility of the wax with the resin, and the vinyl group can enhance the durability and the offset resistance.
For the molecular weight distribution of the modified second wax based on GPC, it is preferable that the weight-average molecular weight is 1000 to 6000, the Z-average molecular weight is 1500 to 9000, the ratio (weight-average molecular weight/number-average molecular weight) of the weight-average molecular weight to the number-average molecular weight is 1.1 to 3.8, the ratio (Z-average molecular weight/number-average molecular weight) of the Z-average molecular weight to the number-average molecular weight is 1.5 to 6.5, there is at least one molecular weight maximum peak in the range of 1×103 to 3×104, the acid value is 10 to 80 mgKOH/g, the melting point is 80° C. to 120° C., and the penetration number is not more than 4 at 25° C. It is more preferable that the weight-average molecular weight is 1000 to 5000, the Z-average molecular weight is 1700 to 8000, the weight-average molecular weight/number-average molecular weight ratio is 1.1 to 2.8, the Z-average molecular weight/number-average molecular weight ratio is 1.5 to 4.5, there is at least one molecular weight maximum peak in the range of 1×103 to 1×104, the acid value is 10 to 50 mgKOH/g, and the melting point is 85° C. to 100° C. It is further preferable that the weight-average molecular weight is 1000 to 2500, the Z-average molecular weight is 1900 to 3000, the weight-average molecular weight/number-average molecular weight ratio is 1.2 to 1.8, the Z-average molecular weight/number-average molecular weight ratio is 1.7 to 2.5, there is at least one molecular weight maximum peak in the range of 1×103 to 3×103, the acid value is 35 to 50 mgKOH/g, and the melting point is 90° C. to 100° C.
The modified second wax can improve the high-temperature offset resistance in the oilless fixing and does not decrease the storage stability. When an image is formed by arranging three layers of color toner on a thin paper, the modified second wax is particularly effective to improve the separability of the paper from the fixing roller or the fixing belt.
By combining the toner to which the modified second wax is added with a carrier, it is possible not only to achieve the oilless fixing but also to suppress the occurrence of spent on the carrier. Thus, the life of a developer can be made longer. Moreover, it is also possible to ensure the compatibility between the fixability and the development stability.
If the carbon number of the long chain alkyl group of the modified wax is less than 4, the releasing action is weakened, so that the separability and the high-temperature offset resistance are degraded. If the carbon number is more than 30, the mixing and aggregation of the wax with the resin become poor, resulting in low dispersibility. If the acid value is less than 10 mgKOH/g, the charge amount of the toner is reduced over a long period of use. If the acid value is more than 80 mgKOH/g, the moisture resistance is decreased to increase fog under high humidity. Moreover, it is difficult to reduce the particle size of the emulsified and dispersed particles of the wax. If the melting point is less than 80° C., the storage stability of the toner is reduced, and the high-temperature offset resistance is degraded. If the melting point is more than 120° C., the low-temperature fixability is weakened, and the color glossiness is lowered. Moreover, it is difficult to reduce the particle size of the emulsified and dispersed particles of the wax. If the penetration number is more than 4 at 25° C., the toughness is reduced to cause filming of the toner on a photoconductive member over a long period of use. If the weight-average molecular weight is less than 1000, the Z-average molecular weight is less than 1500, the weight-average molecular weight/number-average molecular weight ratio is less than 1.1, the Z-average molecular weight/number-average molecular weight ratio is less than 1.5, and the molecular weight maximum peak is in the range smaller than 1×103, the storage stability of the toner is degraded, thus causing filming of the toner on a photoconductive member or intermediate transfer member. The handling property of the toner in a developing unit is reduced. The particle size distribution of the emulsified and dispersed particles becomes broader If the weight-average molecular weight is more than 6000, the Z-average molecular weight is more than 9000, the weight-average molecular weight/number-average molecular weight ratio is more than 3.8, the Z-average molecular weight/number-average molecular weight ratio is more than 6.5, and the molecular weight maximum peak is in the range larger than 3×104, the releasing action is weakened, and the high-temperature offset resistance is degraded. Moreover, it is difficult to reduce the particle size of the emulsified and dispersed particles of the wax.
Examples of the alcohol used for the modified second wax include alcohols having an alkyl chain with a carbon number of 4 to 30 such as octanol (C8H17OH), dodecanol (C12H25OH), stearyl alcohol (C18H37OH), nonacosanol (C29H59OH), and pentadecanol (C15H31OH). Examples of the amines include N-methylhexylamine, nonylamine, stearylamine, and nonadecylamine. In addition, 1-methoxy-(perfluoro-2-methyl-1-propene), hexafluoroacetone, 3-perfluorooctyl-1,2-epoxypropane, or the like can be used preferably as a fluoroalkyl alcohol.
Examples of the unsaturated polycarboxylic acid or its anhydride used for the modified second wax include maleic acid, maleic anhydride, itaconic acid, itaconic anhydride, citraconic acid, and citraconic anhydride. They can be used individually or in combinations of two or more. In particular, the maleic acid and the maleic anhydride are preferred. Examples of the unsaturated hydrocarbon wax include ethylene, propylene, and α-olefin.
The unsaturated polycarboxylic acid or its anhydride is polymerized using alcohol or amine, and then is added to the synthetic hydrocarbon wax in the presence of dicumyl peroxide or tertbutylperoxy isopropyl monocarbonate.
(3) Resin
As the resin particles of the toner of this embodiment, e.g., a thermoplastic binder resin can be used. Specific examples of the thermoplastic binder resin may include the following: styrenes such as styrene, parachloro styrene, and α-methyl styrene; acrylic monomers such as methyl acrylate, ethyl acrylate, n-propyl acrylate, lauryl acrylate, and 2-ethylhexyl acrylate; methacrylic monomers such as methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, lauryl methacrylate, and 2-ethylhexyl methacrylate; ethylene-unsaturated acid monomers such as acrylic acid, methacrylic acid, and sodium styrenesulfonate; vinyl nitrites such as acrylonitrile and methacrylonitrile; vinyl ethers such as vinyl methylether and vinyl isobutylether; vinyl ketones such as vinyl methylketone, vinyl ethylketone, and vinyl isopropenylketone; and olefins such as ethylene, propylene, and butadiene; and a homopolymer of these monomers, a copolymer of two or more types of these monomers, or a mixture of these substances.
The specific examples further may include a non-vinyl condensed resin such as an epoxy resin, a polyester resin, a polyurethane resin, a polyamide resin, a cellulose resin, or a polyether resin, a mixture of the non-vinyl condensed resin and any of the vinyl resins as described above, and a graft copolymer formed by polymerization of vinyl monomers in the presence of the non-vinyl condensed resin.
Among these resins, the vinyl resin is preferred particularly. The vinyl resin is advantageous in that a resin particle dispersion can be prepared easily, e.g., by emulsion polymerization or seed polymerization using an ionic surface-active agent. Examples of the vinyl monomer include a monomer to be used as a material for a vinyl polymer acid or a vinyl polymer base, such as acrylic acid, methacrylic acid, maleic acid, cinnamic acid, fumaric acid, vinyl sulfonic acid, ethylene imine, vinyl pyridine, or vinyl amine. The concentration of resin particles in the resin particle dispersion is 5 to 50 wt %, and preferably 10 to 30 wt %.
To produce core particles having a sharp particle size distribution by the aggregation reaction of the first resin particles, the wax particles, and the colorant particles while eliminating the presence of suspended particles, the first resin particles preferably have a glass transition point of 45° C. to 60° C. and a softening point of 90° C. to 140° C., more preferably a glass transition point of 45° C. to 55° C. and a softening point of 90° C. to 135° C., and further preferably a glass transition point of 45° C. to 52° C. and a softening point of 90° C. to 130° C.
As a preferred configuration of the first resin particles, the weight-average molecular weight (Mw) is 10000 to 60000, and the ratio (Mw/Mn) of the weight-average molecular weight (Mw) to the number-average molecular weight (Mn) is 1.5 to 6. It is more preferable that the weight-average molecular weight (Mw) is 10000 to 50000, and the ratio (Mw/Mn) of the weight-average molecular weight (Mw) to the number-average molecular weight (Mn) is 1.5 to 3.9. It is further preferable that the weight-average molecular weight (Mw) is 10000 to 30000, and the ratio (Mw/Mn) of the weight-average molecular weight (Mw) to the number-average molecular weight (Mn) is 1.5 to 3.
If the transition point of the first resin particles is lower than 45° C., the core particles become coarser. The storage stability and the heat resistance are reduced. If the glass transition point is higher than 55° C., the low-temperature fixability is degraded. If Mw/Mn is larger than 6, the core particles are not stable but irregular in shape, have uneven surfaces, and thus may result in poor surface smoothness.
By including the first resin particles and the wax, the core particles can be prevented from being coarser and can be produced efficiently with a narrow particle size distribution.
It is also possible to ensure the low-temperature fixability, to reduce a change in image glossiness with respect to a fixing temperature, and to make the image glossiness constant. Since the image glossiness generally increases with the fixing temperature, the glossiness of an image varies depending on the fixing temperature. Therefore, the fixing temperature has had to be controlled strictly. However, the above configuration is effective to reduce variations in the image glossiness, even if the fixing temperature changes.
Moreover, it is preferable that the second resin particles are fused with the core particles to form a resin fused layer. As a preferred configuration of the second resin particles, the glass transition point is 45° C. to 65° C., the softening point is 140° C. to 180° C., the weight-average molecular weight (Mw) is 50000 to 500000, and the ratio (Mw/Mn) of the weight-average molecular weight (Mw) to the number-average molecular weight (Mn) is 2 to 10, measured by gel permeation chromatography (GPC). It is more preferable that the glass transition point is 50° C. to 65° C., the softening point is 145° C. to 180° C., Mw is 80000 to 500000, and Mw/Mn is 2 to 7. It is further preferable that the glass transition point is 50° C. to 60° C., the softening point is 150° C. to 180° C., Mw is 120000 to 500000, and Mw/ is 2 to 5.
With this configuration, the thermal adhesiveness of the second resin particles to the surface of the individual core particles is promoted, and the softening point is set to be higher, thereby improving the durability, high-temperature offset resistance, and separability. If the glass transition point of the second resin particles is lower than 45° C., secondary aggregation is likely to occur, and the storage stability is degraded. If it is higher than 65° C., the thermal adhesiveness is degraded, and the uniform adhesion of the second resin particles is reduced. If the softening point of the second resin particles is lower than 140° C., the durability, the high-temperature offset resistance, and the separability are reduced. If it is higher than 180° C., the glossiness and the transmittance are reduced. The molecular weight distribution is brought closer to a monodisperse state by decreasing Mw/Mn of the second resin particles, so that the second resin particles can be fused uniformly with the surface of the individual core particles.
If Mw of the second resin particles is smaller than 50000 the durability, the high-temperature offset resistance, and the separability of paper are reduced. If it is larger than 500000, the low-temperature fixability, the glossiness, and the transmittance are reduced.
The first resin particles are preferably 60 wt % or more, more preferably 70 wt % or more, and further preferably 80 wt % or more of the total resin of the toner.
The molecular weights of the resin, wax, and toner can be measured by gel permeation chromatography (GPC) using several types of monodisperse polystyrene as standard samples.
The measurement may be performed with HLC 8120 GPC series manufactured by TOSOH CORP., using TSK gel super HM-H H4000/H3000/H2000 (6.0 mm I.D.−150 mm×3) as a column and THF (tetrahydrofuran) as an eluent, at a flow rate of 0.6 mL/min, a sample concentration of 0.1%, an injection amount of 20 μL, RI as a detector, and at a temperature of 40° C. Prior to the measurement, the sample is dissolved in THF and allowed to stand overnight, and then is filtered through a 0.45 μm membrane filter so that additives such as silica are removed to measure the resin component. The measurement requirement is that the molecular weight distribution of the subject sample is in the range where the logarithms and the count numbers of the molecular weights in the analytical curve obtained from the several types of monodisperse polystyrene standard samples form a straight line.
The wax obtained by the reaction of long chain alkyl alcohol, unsaturated polycarboxylic acid or its anhydride, and synthetic hydrocarbon wax can be measured with GPC-150C (manufactured by Waters Corporation), using Shodex HT-806M (8.0 mm I.D.−30 cm×2) as a column and o-dichlorobenzene as an eluent, at a flow rate of 1.0 mL/min, a sample concentration of 0.3%, an injection amount of 200 μL, RI as a detector, and at a temperature of 130° C. Prior to the measurement, the sample is dissolved in a solvent, and then is filtered through a 0.5 μm sintered metal filter. The measurement requirement is that the molecular weight distribution of the subject sample is in the range where the logarithms and the count numbers of the molecular weights in the analytical curve obtained from the several types of monodisperse polystyrene standard samples form a straight line. The softening point of the binder resin can be measured with a capillary rheometer flow tester (CFT-500, constant-pressure extrusion system, manufactured by Shimadzu Corporation). A load of about 9.8×105 N/m2 is applied to a 1 cm3 sample with a plunger while heating the sample at a temperature increase rate of 6° C./min, so that the sample is extruded from a die having a diameter of 1 mm and a length of 1 mm. Based on the relationship between the piston stroke of the plunger and the temperature increase characteristics, when the temperature at which the piston stroke starts to occur is a flow start temperature (Tfb), one-half the difference between the minimum value of a curve and the flow end point is determined. Then, the resultant value and the minimum value of the curve are added to define a point, and the temperature of this point is identified as a melting point (softening point Tm) according to a ½ method.
The glass transition point of the resin can be measured with a differential scanning calorimeter (DSC-50 manufactured by Shimadzu Corporation). The temperature of a sample is raised to 100° C., retained for 3 minutes, and reduced to room temperature at 10° C./min. Subsequently, the temperature is raised at 10° C./min, and a thermal history of the sample is measured. In the thermal history, an intersection point of an extension line of the base line lower than a glass transition point and a tangent that shows the maximum inclination between the rising point and the highest point of a peak is determined. The temperature of this intersection point is identified as a glass transition point.
The endothermic peak temperature (melting point ° C.) of the wax based on the DSC method can be measured with a differential scanning calorimeter (DSC-50 manufactured by Shimadzu Corporation). The temperature of a sample is raised to 200° C. at 5° C./min, retained for 5 minutes, and reduced to 10° C. rapidly. Subsequently, the sample is allowed to stand for 15 minutes, and the temperature is raised at 5° C./min. Then, the melting point is determined from the endothermic (melt) peak. The amount of the sample placed in a cell is 10 mg±2 mg.
(4) Pigment
Examples of the colorant (pigment) used in this embodiment include the following. As a black pigment, carbon black, iron black, graphite, nigrosine, or a metal complex of azo dyes can be used preferably. As a yellow pigment, acetoacetic acid aryl amide monoazo yellow pigments such as C. I. Pigment Yellow 1, 3, 74, 97 and 98, acetoacetic acid aryl amide disazo yellow pigments such as C. I. Pigment Yellow 12, 13, 14 and 17, C. I. Solvent Yellow 19, 77 and 79, or C. I. Disperse Yellow 164 can be used preferably. In particular, benzimidazolone pigments of C. I. Pigment Yellow 93, 180 and 185 are suitable. As a magenta pigment, red pigments such as C. I. Pigment Red 48, 49:1, 53:1, 57, 57:1, 81, 122 and 5, or red dyes such as C. I. Solvent Red 49, 52, 58 and 8 can be used preferably. As a cyan pigment, blue dyes/pigments of phthalocyanine and its derivative such as C. I. Pigment Blue 15:3 can be used preferably. The added amount is preferably 3 to 8 parts by weight per 100 parts by weight of the binder resin.
The median diameter of the pigment particles is generally 1 μm or less, and preferably 0.01 to 1 μm. If the median diameter is more than 1 μm, toner as a final product for electrostatic charge image development can have a broader particle size distribution. Moreover, liberated particles are generated and tend to reduce the performance or reliability. When the median diameter is within the above range, these disadvantages are eliminated, and the uneven distribution of the toner is decreased. Therefore, the dispersion of the pigment particles in the toner can be improved, resulting in a smaller variation in performance and reliability. The median diameter can be measured, e.g., by a laser diffraction particle size analyzer (LA 920 manufactured by Horiba, Ltd.).
(5) Additive
In this embodiment, an inorganic fine powder is added as an additive. Examples of the additive include a metal oxide fine powder such as silica, alumina, titanium oxide, zirconia, magnesia, ferrite or magnetite, titanate such as barium titanate, calcium titanate or strontium titanate, zirconate such as barium zirconate, calcium zirconate or strontium zirconate, and a mixture of these substances. The additive can be made hydrophobic as needed.
A preferred silicone oil material that is used to treat the additive is expressed as Chemical Formula (1).
(where R2 is an alkyl group having a carbon number of 1 to 3, R3 is an alkyl group having a carbon number of 1 to 3, a halogen modified alkyl group, a phenyl group, or a substituted phenyl group, R1 is an alkyl group having a carbon number of 1 to 3 or an alkoxy group having a carbon number of 1 to 3, and m and n represent integers of 1 to 100. The formula shows a random copolymer as a whole).
Examples of the silicone oil material include dimethyl silicone oil, methyl hydrogen silicone oil, methyl phenyl silicone oil, cyclic dimethyl silicone oil, epoxy modified silicone oil, carboxyl modified silicone oil, carbinol modified silicone oil, methacrylic modified silicone oil, mercapto modified silicone oil, polyether modified silicone oil, methyl styryl modified silicone oil, alkyl modified silicone oil, fluorine modified silicone oil, amino modified silicone oil, and chlorophenyl modified silicone oil. The additive that is treated with at least one of the above silicone oil materials is used preferably. For example, SH200, SH510, SF230, SH203, BY16-823, or BY16-855B manufactured by Toray-Dow Corning Co., Ltd can be used.
The treatment may be performed by mixing the additive and the silicone oil material with a mixer (e.g., a Henshel mixer, FM20B manufactured by Mitsui Mining Co., Ltd.). Moreover, the silicone oil material may be sprayed onto the additive. Alternatively, the silicone oil material may be dissolved or dispersed in a solvent, and mixed with the additive, followed by removal of the solvent. The amount of silicone oil material is preferably 1 to 20 parts by weight per 100 parts by weight of the additive.
Examples of a silane coupling agent include dimethyldichlorosilane, trimethylchlorosilane, allyldimethylchlorosilane, hexamethyldisilazane, allylphenyldichlorosilane, benzyl methyl chlorosilane, vinyltriethoxysilane, γ-methacryloxypropyltrimethoxysilane, vinyltriacetoxysilane, divinylchlorosilane, and dimethylvinylchlorosilane. The silane coupling agent may be treated by a dry treatment in which the additive is fluidized by agitation or the like, and an evaporated silane coupling agent is reacted with the fluidized additive, or a wet treatment in which a silane coupling agent dispersed in a solvent is added dropwise to the additive.
It is also preferable that the silicone oil material is treated after a silane coupling treatment.
The additive having positive chargeability may be treated with aminosilane, amino modified silicone oil expressed as Chemical Formula (2), or epoxy modified silicone oil.
(where R1 and R6 are hydrogen, an alkyl group having a carbon number of 1 to 3, an alkoxy group, or an aryl group, R2 is an alkylene group having a carbon number of 1 to 3 or a phenylene group, R3 is an organic group including a nitrogen heterocyclic ring, R4 and R5 are hydrogen, an alkyl group having a carbon number of 1 to 3, or an aryl group, m represents positive numbers of not less than 1, and n and q represent positive integers including 0. The formula shows a random copolymer as a whole).
To enhance a hydrophobic treatment, hexamethyldisilazane, dimethyldichlorosilane, or other silicone oil also can be used along with the above materials. For example, at least one selected from dimethyl silicone oil, methylphenyl silicone oil, and alkyl modified silicone oil is preferred to treat the additive.
It is also preferable that the surface of the additive is treated with one or more selected from fatty acid ester, fatty acid amide, fatty acid, and fatty acid metal salt (referred to as “fatty acid or the like” in the following). The surface-treated silica or titanium oxide fine powder is more preferred.
Examples of the fatty acid and the fatty acid metal salt include caprylic acid, capric acid, undecylic acid, lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, montanic acid, lacceric acid, oleic acid, erucic acid, sorbic acid, and linoleic acid. In particular, fatty acid having a carbon number of 12 to 22 is preferred.
Metals of the fatty acid metal salt may be, e.g., aluminum, zinc, calcium, magnesium, lithium, sodium, lead, or barium. Among these metals, aluminum, zinc, and sodium are preferred. Further, mono- and di-fatty acid aluminum such as aluminum distearate (Al(OH)(C17H35COO)2) or aluminum monostearate (Al(OH)2(C17H35COO)) are particularly preferred. By containing a hydroxy group, they can prevent overcharge and suppress a transfer failure. Moreover, it may be possible to improve the treatment of the additive.
Preferred examples of aliphatic amide include saturated or mono-unsaturated aliphatic amide having a carbon number of 16 to 24 such as palmitic acid amide, palmitoleic acid amide, stearic acid amide, oleic acid amide, arachidic acid amide, eicosanoic acid amide, behenic acid amide, erucic acid amide, or lignoceric acid amide.
Preferred examples of the fatty acid ester include the following: esters composed of higher alcohol having a carbon number of 16 to 24 and higher fatty acid having a carbon number of 16 to 24 such as stearyl stearate, palmityl palmitate, behenyl behenate, or stearyl montanate; esters composed of higher fatty acid having a carbon number of 16 to 24 and lower monoalcohol such as butyl stearate, isobutyl behenate, propyl montanate, or 2-ethylhexyl oleate; fatty acid pentaerythritol monoester; fatty acid pentaerythritol triester; and fatty acid trimethylol propane ester.
Moreover, materials such as a derivative of hydroxystearic acid and polyol fatty acid ester such as glycerin fatty acid ester, glycol fatty acid ester, or sorbitan fatty acid ester are preferred. They can be used individually or in combinations of two or more.
In a preferred surface treatment, the surface of the additive preferably is treated with the fatty acid or the like after it has been treated with a coupling agent and/or polysiloxane such as silicone oil. This is because a more uniform treatment can be performed than when hydrophilic silica merely is treated with a fatty acid, high charging of the toner can be achieved, and the flowability can be improved when the additive is added to the toner. The above effect also can be obtained by treating with the fatty acid or the like along with a coupling agent and/or silicone oil.
The surface treatment may be performed by dissolving the fatty acid or the like in a hydrocarbon organic solvent such as toluene, xylene, or hexane, wet mixing this solution with an additive such as silica, titanium oxide, or alumina in a dispersing device, and allowing the fatty acid or the like to adhere to the surface of the additive with the treatment agent. After the surface treatment, the solvent is removed, and a drying process is performed.
It is preferable that the mixing ratio of polysiloxane to the fatty acid or the like is 1:2 to 20:1. If the fatty acid or the like is increased to a ratio higher than 1:2, the charge amount of the additive becomes high, the image density is reduced, and charge-up is likely to occur in two-component development. If the fatty acid or the like is decreased to a ratio lower than 20:1, the effect of suppressing transfer voids or reverse transfer is reduced.
In this case, the ignition loss of the additive whose surface has been treated with the fatty acid or the like is preferably 1.5 to 25 wt %, more preferably 5 to 25 wt %, and further preferably 8 to 20 wt %. If the ignition loss is smaller than 1.5 wt %, the treatment agent does not function sufficiently, and the chargeability and the transfer property cannot be improved. If the ignition loss is larger than 25 wt %, the treatment agent remains unused and adversely affects the developing property or durability.
Unlike the conventional pulverizing process, the surface of the individual toner base particles produced in the present invention consists mainly of resin. Therefore, it is advantageous in terms of charge uniformity, but affinity with the additive used for the charge-imparting property or charge-retaining property becomes important.
It is preferable that the additive having an average particle size of 6 nm to 200 nm is added in an amount of 1 to 6 parts by weight per 100 parts by weight of toner base particles. If the average particle size is less than 6 nm, suspended particles are generated, and filming of the toner on a photoconductive member is likely to occur. Therefore, it is difficult to avoid the occurrence of reverse transfer. If the average particle size is more than 200 nm, the flowability of the toner is decreased. If the amount of the additive is less than 1 part by weight, the flowability of the toner is decreased, and it is difficult to avoid the occurrence of reverse transfer. If the amount of the additive is more than 6 parts by weight, suspended particles are generated, and filming of the toner on a photoconductive member is likely to occur, thus degrading the high-temperature offset resistance.
Moreover, it is preferable that at least the additive having an average particle size of 6 nm to 20 nm is added in an amount of 0.5 to 2.5 parts by weight per 100 parts by weight of the toner base particles, and the additive having an average particle size of 20 nm to 200 nm is added in an amount of 0.5 to 3.5 parts by weight per 100 parts by weight of toner base particles. With this configuration, the additives of different functions can improve both the charge-imparting property and the charge-retaining property, and also can ensure larger tolerances against reverse transfer, transfer voids, and scattering of the toner during transfer. In this case, the ignition loss of the additive having an average particle size of 6 nm to 20 nm is preferably 0.5 to 20 wt %, and the ignition loss of the additive having an average particle size of 20 nm to 200 nm is preferably 1.5 to 25 wt %. When the ignition loss of the additive having an average particle size of 20 nm to 200 nm is larger than that of the additive having an average particle size of 6 nm to 20 nm, it is effective in improving the charge-retaining property and suppressing reverse transfer and transfer voids.
By specifying the ignition loss of the additive, larger tolerances can be ensured against reverse transfer, transfer voids, and scattering of the toner during transfer. Moreover, the handling property of the toner in a developing unit can be improved, thus increasing the uniformity of the toner concentration. The generation of a developing memory also can be reduced.
If the ignition loss of the additive having an average particle size of 6 nm to 20 nm is less than 0.5 wt %, the tolerances against reverse transfer and transfer voids become narrow. If the ignition loss is more than 20 wt %, the surface treatment is not uniform, resulting in charge variations. The ignition loss is preferably 1.5 to 17 wt %, and more preferably 4 to 10 wt %.
If the ignition loss of the additive having an average particle size of 20 nm to 200 nm is less than 1.5 wt %, the tolerances against reverse transfer and transfer voids become narrow. If the ignition loss is more than 25 wt %, the surface treatment is not uniform, resulting in charge variations. The ignition loss is preferably 2.5 to 20 wt %, and more preferably 5 to 15 wt %.
Further, it is preferable that at least the additive having an average particle size of 6 nm to 20 nm and an ignition loss of 0.5 to 20 wt % is added in an amount of 0.5 to 2 parts by weight per 100 parts by weight of the toner base particles, the additive having an average particle size of 20 nm to 100 nm and an ignition loss of 1.5 to 25 wt % is added in an amount of 0.5 to 3.5 parts by weight per 100 parts by weight of the toner base particles, and the additive having an average particle size of 100 nm to 200 nm and an ignition loss of 0.1 to 10 wt % is added in an amount of 0.5 to 2.5 parts by weight per 100 parts by weight of toner base particles. With this configuration, the additives of different functions, having the specified average particle size and ignition loss, can improve both the charge-imparting property and the charge-retaining property, suppress reverse transfer and transfer void, and remove a substance attached to the surface of a carrier.
It is also preferable that a positively charged additive having an average particle size of 6 nm to 200 nm and an ignition loss of 0.5 to 25 wt % is added further in an amount of 0.2 to 1.5 parts by weight per 100 parts by weight of toner base particles.
The addition of the positively charged additive can suppress the overcharge of the toner for a long period of continuous use and increase the life of a developer. Therefore, the scattering of the toner during transfer caused by overcharge also can be reduced. Moreover, it is possible to prevent spent on a carrier. If the amount of positively charged additive is less than 0.2 parts by weight, these effects are not likely to be obtained. If it is more than 1.5 parts by weight, fog is increased significantly during development. The ignition loss is preferably 1.5 to 20 wt %, and more preferably 5 to 19 wt %.
A drying loss (%) may be determined in the following manner. A container is dried, allowed to stand and cool, and weighed precisely beforehand. Then, a sample (about 1 g) is put in the container, weighed precisely, and dried for 2 hours with a hot-air dryer at 105° C.±1° C. After cooling for 30 minutes in a desiccator, the weight is measured, and the drying loss is calculated by the following formula.
Drying loss (%)=[weight loss(g) by drying/sample amount(g)]×100.
An ignition loss may be determined in the following manner. A magnetic crucible is dried, allowed to stand and cool, and weighed precisely beforehand. Then, a sample (about 1 g) is put in the crucible, weighed precisely, and ignited for 2 hours in an electric furnace at 500° C. After cooling for 1 hour in a desiccator, the weight is measured, and the ignition loss is calculated by the following formula.
Ignition loss (%)=[weight loss(g) by ignition/sample amount(g)]×100.
The amount of moisture absorption of the surface-treated additive may be 1 wt % or less, preferably 0.5 wt % or less, more preferably 0.1 wt % or less, and further preferably 0.05 wt % or less. If the amount is more than 1 wt %, the chargeability is degraded, and filming of the toner on a photoconductive member occurs over time. The amount of moisture absorption can be measured by using a continuous vapor absorption measuring device (BELSORP 18 manufactured by BEL JAPAN, INC.).
The degree of hydrophobicity may be determined in the following manner. A sample (0.2 g) is weighed precisely in a 250 ml beaker containing 50 ml of distilled water. Then, methanol is added dropwise from a buret, whose end is put into the water, until the entire amount of the additive is wetted while continuing the stirring slowly with a magnetic stirrer. Based on the amount a (ml) of methanol required to wet the additive completely, the degree of hydrophobicity is calculated by the following formula.
Degree of hydrophobicity(%)=(a/(50+a))×100
(6) Powder Physical Characteristics of Toner
In this embodiment, it is preferable that toner base particles including a binder resin, a colorant, and wax have a volume-average particle size of 3 to 7 μm, the content of the toner base particles having a particle size of 2.52 to 4 μm in a number distribution is 10 to 75% by number, the toner base particles having a particle size of 4 to 6.06 μm in a volume distribution is 25 to 75% by volume, the toner base particles having a particle size of not less than 8 μm in the volume distribution is not more than 5% by volume, P46/V46 is in the range of 0.5 to 1.5 where V46 is the volume percentage of the toner base particles having a particle size of 4 to 6.06 μm in the volume distribution and P46 is the number percentage of the toner base particles having a particle size of 4 to 6.06 μm in the number distribution, the coefficient of variation in the volume-average particle size is 10 to 25%, and the coefficient of variation in the number particle size distribution is 10 to 28%.
More preferably the toner base particles have a volume-average particle size of 3 to 6.5 μm, the content of the toner base particles having a particle size of 2.52 to 4 μm in the number distribution is 20 to 75% by number, the toner base particles having a particle size of 4 to 6.06 μm in the volume distribution is 35 to 75% by volume, the toner base particles having a particle size of not less than 8 μm in the volume distribution is not more than 3% by volume, P46/V46 is in the range of 0.5 to 1.3, the coefficient of variation in the volume-average particle size is 10 to 20%, and the coefficient of variation in the number particle size distribution is 10 to 23%.
Further preferably, the toner base particles have a volume-average particle size of 3 to 5 μm, the content of the toner base particles having a particle size of 2.52 to 4 μm in the number distribution is 40 to 75% by number, the toner base particles having a particle size of 4 to 6.06 μm in the volume distribution is 45 to 75% by volume, the toner base particles having a particle size of not less than 8 μm in the volume distribution is not more than 3% by volume, P46/V46 is in the range of 0.5 to 0.9, the coefficient of variation in the volume-average particle size is 10 to 15%, and the coefficient of variation in the number particle size distribution is 10 to 18%.
The toner base particles with the above characteristics can provide high-resolution image quality, prevent reverse transfer and transfer voids during tandem transfer, and achieve the oilless fixing. The fine powder in the toner affects the flowability, image quality, and storage stability of the toner, filming of the toner on a photoconductive member, developing roller, or transfer member, the aging property, the transfer property, and particularly the multilayer transfer property in a tandem system. The fine powder also affects the offset resistance, glossiness, and transmittance in the oilless fixing. When the toner includes wax or the like to achieve the oilless fixing, the amount of fine powder may affect the compatibility between the oilless fixing and the tandem transfer property.
If the volume-average particle size is more than 7 μm, the image quality and the transfer property cannot be ensured together. If the volume-average particle size is less than 3 μm, the handling property of the toner particles in development is reduced.
If the content of the toner base particles having a particle size of 2.52 to 4 μm in the number distribution is less than 10% by number, the image quality and the transfer property cannot be ensured together. If it is more than 75% by number, the handling property of the toner particles in development is reduced. Moreover, the filing of the toner on a photoconductive member, developing roller, or transfer member is likely to occur. The adhesion of the fine powder to a heat roller is large, and thus tends to cause offset. In the tandem system, the agglomeration of the toner is likely to be stronger, which easily leads to a transfer failure of the second color during multilayer transfer. Therefore, an appropriate range is necessary.
If the toner base particles having a particle size of 4 to 6.06 μm in the volume distribution is more than 75% by volume, the image quality and the transfer property cannot be ensured together. If it is less than 25% by volume, the image quality is degraded.
If the toner base particles having a particle size of not less than 8 μm in the volume distribution is more than 5% by volume, the image quality is degraded to cause a transfer failure.
If P46/V46 is less than 0.5, where V46 is the volume percentage of the toner base particles having a particle size of 4 to 6.06 μm the volume distribution and P46 is the number percentage of the toner base particles having a particle size of 4 to 6.06 μm in the number distribution, the amount of fine powder is increased excessively, so that the flowability and the transfer property are decreased, and fog becomes worse. If P46/V46 is more than 1.5, the number of large particles is increased, and the particle size distribution becomes broader. Thus, high image quality cannot be achieved.
The purpose of controlling P46/V46 is to provide an index for reducing the size of the toner particles and narrowing the particle size distribution.
The coefficient of variation is obtained by dividing a standard deviation by an average particle size of the toner particles based on the measurement using a Coulter Counter (manufactured by Coulter Electronics, Inc.). When the particle sizes of n particles are measured, the standard deviation can be expressed by the square root of the value that is obtained by dividing the square of a difference between each of the n measured values and the mean value by (n−1).
In other words, the coefficient of variation indicates the degree of expansion of the particle size distribution. When the coefficient of variation of the volume particle size distribution or the number particle size distribution is less than 10%, the production becomes difficult, and the cost is increased. When the coefficient of variation of the volume particle size distribution is more than 25%, or when the coefficient of variation of the number particle size distribution is more than 28%, the particle size distribution is broader, and the agglomeration of toner is stronger. This may lead to filming of the toner on a photoconductive member, a transfer failure, and difficulty of recycling the residual toner in a cleanerless process.
The particle size distribution is measured, e.g., by using a Coulter Counter TA-II (manufactured by Coulter Electronics, Inc.). An interface (manufactured by Nikkaki Bios Co., Ltd.) for outputting a number distribution and a volume distribution and a personal computer are connected to the Coulter Counter TA-II. An electrolytic solution (about 50 ml) is prepared by including a surface-active agent (sodium lauryl sulfate) so as to have a concentration of 1%. About 2 mg of toner to be measured is added to the electrolytic solution. This electrolytic solution in which the sample is suspended is dispersed for about 3 minutes with an ultrasonic dispersing device, and then is measured using the 70 μm aperture of the Coulter Counter TA-II. In the 70 μm aperture system, the measurement range of the particle size distribution is 1.26 μm to 50.8 μm. However, the region smaller than 2.0 μm is not suitable for practical use because the measurement accuracy or reproducibility is low due to the influence of external noise or the like. Therefore, the measurement range is set from 2.0 μm to 50.8 μm.
A compression ratio calculated from a static bulk density and a dynamic bulk density can be used as an index of the flowability of the toner. The toner flowability may be affected by the particle size distribution and particle shape of the toner, the additive, and the type or amount of wax. When the particle size distribution of the toner is narrow, less fine powder is present, the toner surface is not rough, the toner shape is close to spherical, a large amount of additive is added, and the additive has a small particle size, the compression ratio is reduced, and the toner flowability is increased. The compression ratio is preferably 5 to 40%, and more preferably 10 to 30%. This can ensure the compatibility between the oilless fixing and the multilayer transfer property in the tandem system. If the compression ratio is less than 5%, the fixability is degraded, and particularly the transmittance is likely to be lower. Moreover toner scattering from the developing roller may be increased. If the compression ratio is more than 40%, the transfer property is decreased to cause a transfer failure such as transfer voids in the tandem system.
(7) Carrier
A carrier of this embodiment includes magnetic particles as a core material, and the surface of the core material is coated with a fluorine modified silicone resin containing an aminosilane coupling agent.
Moreover, the carrier may include composite magnetic particles including at least magnetic particles and a binder resin, and the surfaces of the composite magnetic particles are coated with the fluorine modified silicone resin containing an aminosilane coupling agent.
A thermosetting resin is suitable for the binder resin of the composite magnetic particles. Examples of the thermosetting resin include a phenol resin, an epoxy resin, a polyamide resin, a melamine resin, a urea resin, an unsaturated polyester resin, an alkyd resin, a xylene resin, an acetoguanamine resin, a furan resin, a silicone resin, a polyimide resin, and a urethane resin. Although these resins can be used individually or in combinations of two or more, it is preferable to include at least the phenol resin.
The composite magnetic particles of the present invention may be spherical particles having an average particle size of 10 to 50 μm, preferably 10 to 40 μm, more preferably 10 to 30 μm, and most preferably 15 to 30 μm. The specific gravity of the composite magnetic particles may be 2.5 to 4.5, and particularly 2.5 to 4.0. The BET specific surface area based on nitrogen adsorption of the carrier is preferably 0.03 to 0.3 m2/g. If the average particle size of the carrier is less than 10 μm, the abundance ratio of fine particles in the carrier particle distribution is increased, and the magnetization per carrier particle is reduced. Therefore, the carrier is likely to be developed on a photoconductive member. If the average particle size of the carrier is more than 50 μm, the specific surface area of the carrier particles is smaller, and the toner retaining ability is decreased, causing toner scattering. For full color images including many solid portions, the reproduction of the solid portions is particularly poor.
A conventional carrier including ferrite core particles has a large specific gravity of 5 to 6, and also has a large particle size of 50 to 80 μm. Therefore, the BET specific surface area is small, and the mixing of the carrier with the toner is weak during stirring. Thus, the charge build-up property is insufficient when the toner is supplied, and toner consumption is increased. For this reason, at the time of supplying a large amount of toner, considerable fog is likely to be generated. Moreover, if the concentration ratio of the toner to the carrier is not controlled in a narrow range, it is difficult to reduce fog and toner scattering while maintaining the image density.
However, the carrier having a large specific surface area value can suppress the degradation of image quality, even if the concentration ratio is controlled in a broad range, so that the toner concentration can be controlled roughly. Moreover, the carrier and the toner can be mixed more uniformly by stirring, and the charge build-up property is good when the toner is supplied. Even if the concentration ratio is controlled in a broader range, the image quality is not likely to be degraded, and fog and toner scattering can be reduced while maintaining the image density.
In this case, the image quality can be stabilized by satisfying the relationship TS/CS=2 to 110, where TS (m2/g) represents the specific surface area value of the toner and CS (m2/g) represents the specific surface area value of the carrier. TS/CS is preferably 2 to 50, and more preferably 2 to 30. If TS/CS is less than 2, the adhesion of the carrier is likely to occur. If it is more than 110, the concentration ratio of the toner to the carrier has to be narrow so as to reduce fog and toner scattering while maintaining the image density. Thus, the image quality can be degraded easily. The conventional carrier including ferrite core particles has a small specific surface area value. The conventional pulverized toner is irregular in shape and has a large specific surface area value.
The composite magnetic particles including magnetic particles and a phenol resin may be produced in such a manner that phenols and aldehydes react and cure while they are stirred into an aqueous medium in the presence of the magnetic particles and a basic catalyst.
The average particle size of the composite magnetic particles can be controlled by controlling the agitating speed of an agitator so that appropriate shear or consolidation is applied in accordance with the amount of water used.
The composite magnetic particles using an epoxy resin as the binder resin may be produced in such a manner that bisphenol, epihalohydrin, and lipophilized inorganic compound particles are dispersed in an aqueous medium and allowed to react in an alkaline aqueous medium.
The composite magnetic particles of the present invention may include 1 to 20 wt % of a binder resin and 80 to 99 wt % of magnetic particles. If the content of the magnetic particles is less than 80 wt %, the saturation magnetization is reduced. If it is more than 99 wt %, the binding between the magnetic particles with the phenol resin is likely to be weaker. In view of the strength of the composite magnetic particles, the content of the magnetic particles is preferably 97 wt % or less.
Examples of the magnetic particles include spinel ferrite such as magnetite or gamma iron oxide, spinel ferrite including one or more than one metal (Mn, Ni, Zn, Mg, Cu, etc.) other than iron, magnetoplumbite ferrite such as barium ferrite, and iron or alloy fine particles having an oxide layer on the surface thereof. The magnetic particles may be granular, spherical, or acicular in shape. Ferromagnetic fine particles of iron or the like also can be used, particularly when high magnetization is required. In view of the chemical stability, however, it is preferable to use ferromagnetic fine particles of the spinel ferrite such as magnetite or gamma iron oxide or the magnetoplumbite ferrite such as barium ferrite. The composite magnetic particles with desired saturation magnetization can be obtained by selecting the type and content of the ferromagnetic fine particles appropriately.
According to the measurement under a magnetic field of 1000 oersted (79.57 kA/m), the magnetization strength may be 30 to 70 Am2/kg, and preferably 35 to 60 Am2/kg, the residual magnetization (ar) may be 0.1 to 20 Am2/kg, and preferably 0.1 to 10 Am2/kg, and the specific resistance value may be 1×106 to 1×1014 Ωcm, preferably 5×106 to 5×1013 Ω·cm, and more preferably 5×106 to 5×109 Ω·cm.
In a method for producing the carrier of the present invention, phenols and aldehydes, together with magnetic particles and a suspension stabilizer, react in an aqueous medium in the presence of a basic catalyst.
Examples of the phenols used as the binder resin include phenol, alkylphenol such as m-cresol, p-tert-butyl phenol, o-propylphenol, resorcinol, or bisphenol A, and a compound having a phenolic hydroxyl group such as halogenated phenol in which part or all of the benzene nucleus or the alkyl group is substituted with chlorine or bromine atoms. Above all, phenol is most preferred. When compounds other than phenol are used, particles are not formed easily or may have an irregular shape, even if they are formed. Therefore, phenol is most preferred in view of the shape of the particles.
Examples of the aldehydes used in the method for producing the composite magnetic particles include formaldehyde in the form of either formalin or paraformaldehyde and furfural. Above all, formaldehyde is particularly preferred.
A fluorine modified silicone resin is essential for the resin coating of the present invention. The fluorine modified silicone resin may be a cross-linked fluorine modified silicone resin obtained by the reaction between an organosilicon compound containing a perfluoroalkyl group and polyorganosiloxane. It is preferable that 3 to 20 parts by weight of the organosilicon compound containing a perfluoroalkyl group is mixed with 100 parts by weight of the polyorganosiloxane. Compared to the coating on the conventional ferrite core particles, the adhesion of the composite magnetic particles in which magnetic particles are dispersed in a curable resin is strengthened, thus improving the durability along with the chargeability (as will be described later).
The polyorganosiloxane preferably has at least one repeating unit selected from the following Chemical Formulas (3) and (4).
(where R1 and R2 are a hydrogen atom, a halogen atom, a hydroxy group, a methoxy group, an alkyl group having a carbon number of 1 to 4, or a phenyl group, R3 and R4 are an alkyl group having a carbon number of 1 to 4 or a phenyl group, and m represents a mean degree of polymerization and is positive integers (preferably in the range of 2 to 500, and more preferably in the range of 5 to 200)).
(where R1 and R2 are a hydrogen atom, a halogen atom, a hydroxy group, a methoxy group, an alkyl group having a carbon number of 1 to 4, or a phenyl group, R3, R4, R5 and R11 are an alkyl group having a carbon number of 1 to 4 or a phenyl group, and n represents a mean degree of polymerization and is positive integers (preferably in the range of 2 to 500, and more preferably in the range of 5 to 200)).
Examples of the organosilicon compound containing a perfluoroalkyl group include CF3CH2CH2Si(OCH3)3, C4F9CH2CH2Si(CH3)(OCH3)2, C8F17CH2CH2Si(OCH3)3, C8F17CH2CH2Si(OC2H5)3, and (CF3)2CF(CF2)sCH2CH2Si(OCH3)3. In particular, a compound containing a trifluoropropyl group is preferred.
In this embodiment, the aminosilane coupling agent is included in the resin coating. As the aminosilane coupling agent, e.g., the following known materials can be used: γ-(2-aminoethyl)aminopropyltrimethoxysilane, γ-(2-aminoethyl)aminopropylmethyldimethoxysilane, and octadecylmethyl[3-(trimethoxysilyl)propyl]ammonium chloride (corresponding to SH6020, SZ6023, and AY43-021 manufactured by Toray-Dow Corning Co., Ltd.); KBM602, KBM603, KBE903, and KBM573 (manufactured by Shin-Etsu Chemical Co., Ltd.). In particular, the primary amine is preferred. The secondary or tertiary amine that is substituted with a methyl group, an ethyl group, or a phenyl group has weak polarity and is less effective for the charge build-up property of the toner. When the amino group is replaced by an aminomethyl group, an aminoethyl group, or an aminophenyl group, the end of a straight chain extended from silane of the silane coupling agent can be the primary amine. However, the amino group contained in the organic group of the straight chain does not contribute to the charge build-up property and is affected by moisture under high humidity. Therefore, although the carrier may have charging ability for the initial toner because the amino group is at the end, the charging ability is decreased during printing, resulting in a short life of the carrier.
By using the above aminosilane coupling agent with the fluorine modified silicone resin of this embodiment, the toner can be charged negatively while maintaining a sharp charge distribution. When the toner is supplied, it shows a quick rise in charge, and thus the toner consumption can be reduced. Moreover, the aminosilane coupling agent has the effect comparable to that of a cross-linking agent, and therefore can increase the degree of cross-linking of the coating of the fluorine modified silicone resin as a base resin. The hardness of the resin coating is improved further, so that abrasion or peeling can be reduced over a long period of use. Accordingly, higher resistance to spent can be obtained, and the electrification can be stabilized by suppressing a decrease in the charging ability of the carrier, thus improving the durability. In particular, when the toner is configured by fusing the second resin particles with the core particles to form a resin fused layer, the carrier serves to improve the charge build-up property, reduce fog, and increase the uniformity of a solid image. Moreover, it also can suppress transfer voids or skipping in characters during transfer, improve the handling property of the toner in a developing unit, and reduce a so-called developing memory, in which a history remains after forming a solid image.
The ratio of the aminosilane coupling agent to the resin is 5 to 40 wt %, and preferably 10 to 30 wt %. If the ratio is less than 5 wt %, no effect of the aminosilane coupling agent is observed. If the ratio is more than 40 wt %, the degree of cross-linking of the resin coating is excessively high, and a charge-up phenomenon is likely to occur. This may lead to image defects such as underdevelopment and low image density.
The resin coating also may include conductive fine powder to stabilize the electrification and to prevent charge-up. Examples of the conductive fine powder include carbon black such as oil furnace black or acetylene black, a semiconductive oxide such as titanium oxide or zinc oxide, and powder of titanium oxide, zinc oxide, barium sulfate, aluminum borate, or potassium titanate coated with tin oxide, carbon black, or metal. The specific resistance is preferably not more than 1010 Ω·cm. The content of the conductive fine powder is preferably 1 to 15 wt %. When the conductive fine powder is included to some extent in the resin coating, the hardness of the resin coating can be improved by a filler effect. However, if the content is more than 15 wt %, the conductive fine powder may interfere with the formation of the resin coating, resulting in lower adherence and hardness. An excessive amount of conductive fine powder in a full color developer may cause the color contamination of the toner that is transferred and fixed on paper.
A method for forming a coating layer on the composite magnetic particles is not particularly limited, and any known coating methods can be used, such as a dipping method of dipping the composite magnetic particles in a solution for forming a coating layer, a spraying method of spraying a solution for forming a coating layer on the surfaces of the composite magnetic particles, a fluidized bed method of spraying a solution for forming a coating layer onto the composite magnetic particles that are floated by fluidizing air, and a kneader and coater method of mixing the composite magnetic particles and a solution for forming a coating layer in a kneader and coater, and removing a solvent. In addition to these wet coating methods, a dry coating method also can be used. The dry coating method includes, e.g., mixing resin powder and the composite magnetic particles at high speed, and fusing the resin powder on the surfaces of the composite magnetic particles by utilizing the frictional heat. In particular, the wet coating method is preferred for coating of the fluorine modified silicone resin containing an aminosilane coupling agent of the present invention.
A solvent of the solution for forming a coating layer is not particularly limited as long as it dissolves the coating resin, and can be selected in accordance with the coating resin to be used. Examples of the solvent include aromatic hydrocarbons such as toluene and xylene, ketones such as acetone and methyl ethyl ketone, and ethers such as tetrahydrofuran and dioxane.
The amount of coating resin is preferably 0.2 to 6.0 wt %, more preferably 0.5 to 5.0 wt %, further preferably 0.6 to 4.0 wt %, and most preferably 0.7 to 3 wt % with respect to the composite magnetic particles. If the amount of coating resin is less than 0.2 wt %, a uniform coating cannot be formed on the surfaces of the composite magnetic particles. Therefore, the carrier is affected significantly by the characteristics of the composite magnetic particles and cannot provide a sufficient effect of the fluorine modified silicone resin containing an aminosilane coupling agent. If the amount of coating resin is more than 6.0 wt %, the coating is too thick, and granulation between the composite magnetic particles occurs. Therefore, the composite magnetic particles are not likely to be uniform.
It is preferable that a baking treatment is performed after coating the surfaces of the composite magnetic particles with the fluorine modified silicone resin containing an aminosilane coupling agent. A system for the baling treatment is not particularly limited, and either of external and internal heating systems may be used. For example, a fixed or fluidized electric furnace, a rotary kiln electric furnace, or a burner furnace can be used as well. Alternatively, baking may be performed with a microwave. The baking temperature should be high enough to provide the effect of fluorine modified silicone that can improve the spent resistance of the resin coating, e.g., preferably 200° C. to 350° C., and more preferably 220° C. to 280° C. The treatment time is preferably 1.5 to 2.5 hours. A lower temperature may degrade the hardness of the resin coating itself, while an excessively high temperature may cause a charge reduction.
(8) Two-Component Development
In a development process, both direct-current bias and alternating-current bias are applied between a photoconductive member and a developing roller. In this case, it is preferable that the frequency is 1 to 10 kHz, the alternating-current bias is 1.0 to 2.5 kV (p-p), and the circumferential velocity ratio of the photoconductive member to the developing roller is 1:1.2 to 1:2. More preferably the frequency is 3.5 to 8 kHz, the alternating-current bias is 1.2 to 2.0 kV (p-p), and the circumferential velocity ratio of the photoconductive member to the developing roller is 1:1.5 to 1:1.8. Further preferably, the frequency is 5.5 to 7 kHz, the alternating-current bias is 1.5 to 2.0 kV (p-p), and the circumferential velocity ratio of the photoconductive member to the developing roller is 1:1.6 to 1:1.8.
By using the above development process configuration with the toner or two-component developer of this embodiment, a high image density can be achieved, fog can be reduced, and dots can be reproduced faithfully. Thus, a high quality image and the oilless fixability can be ensured together.
If the frequency is less than 1 kHz, the dot reproducibility is decreased, resulting in poor reproduction of middle tones. If the frequency is more than 10 kHz, the toner cannot follow in the development region, and no effect is observed. In the two-component development using a high resistance carrier, the frequency within the above range is more effective for reciprocating action between the carrier and the toner than between the developing roller and the photoconductive member. Thus, the toner can be liberated slightly from the carrier. This improves the dot reproducibility and the middle tone reproducibility, and also provides a high image density.
If the alternating-current bias is lower than 1.0 kV (p-p), the effect of suppressing charge-up cannot be obtained. If the alternating-current bias is more than 2.5 kV (p-p), fog is increased. If the circumferential velocity ratio is less than 1:1.2 (the developing roller gets slower), it is difficult to ensure the image density. If the circumferential velocity ratio is more than 1:2 (the developing roller gets faster), toner scattering is increased.
(9) Tandem Color Process
This embodiment employs the following transfer process for high-speed color image formation. A plurality of toner image forming stations, each of which includes a photoconductive member, a charging member, and a toner support member, are used. In a primary transfer process, an electrostatic latent image formed on the photoconductive member is made visible by development, and a toner image thus developed is transferred to an endless transfer member that is in contact with the photoconductive member. The primary transfer process is performed continuously in sequence so that a multilayer toner image is formed on the transfer member. Then, a secondary transfer process is performed by collectively transferring the multilayer toner image from the transfer member to a transfer medium such as paper or OHP sheet. The transfer process satisfies the relationship expressed as
d1/v≦0.65
where d1 (mm) is a distance between the first primary transfer position and the second primary transfer position, and v (mm/s) is a circumferential velocity of the photoconductive member. This configuration can reduce the machine size and improve the printing speed. To process at least 20 sheets (A4) per minute and to make the size small enough to be used for SOHO (small office/home office) purposes, a distance between the toner image forming stations should be as short as possible, while the processing speed should be enhanced. Thus, d1/v≦0.65 is considered to be the minimum requirement to achieve both small size and high printing speed.
However, when the distance between the toner image forming stations is too short, e.g., when a period of time from the primary transfer of the first color (yellow toner) to that of the second color (magenta toner) is extremely short, the charge of the transfer member or the charge of the transferred toner hardly is eliminated. Therefore, when the magenta toner is transferred onto the yellow toner, it is repelled by the charging action of the yellow toner. This may lead to lower transfer efficiency and transfer voids. When the third color (cyan toner) is transferred onto the yellow and the magenta toner, the cyan toner may be scattered to cause a transfer failure or considerable transfer voids. Moreover, the toner having a specified particle size is developed selectively with repeated use, and the individual toner particles differ significantly in flowability, so that frictional charge opportunities are different. Thus, the charge amount is varied and the transfer property is reduced further.
In such a case, therefore, the toner or two-component developer of this embodiment can be used to stabilize the charge distribution and suppress the overcharge and flowability variations. Accordingly, it is possible to prevent lower transfer efficiency, transfer voids, and reverse transfer without sacrificing the fixing property.
(10) Oilless Color Fixing
The toner of this embodiment can be used preferably in an electrographic apparatus having a fixing process with an oilless fixing configuration that applies no oil to any fixing means. For heating, electromagnetic induction heating is suitable in view of reducing the warm-up time and power consumption. The oilless fixing configuration includes a magnetic field generation means and a heating and pressing means. The heating and pressing means includes a rotational heating member and a rotational pressing member. The rotational heating member includes at least a heat generation layer for generating heat by electromagnetic induction and a release layer. There is a certain nip between the rotational heating member and the rotational pressing member. The toner that has been transferred to a transfer medium such as copy paper is fixed by passing the transfer medium between the rotational heating member and the rotational pressing member. This configuration is characterized by the warm-up time of the rotational heating member that has a quick rising property as compared with a conventional configuration using a halogen lamp. Therefore, the copying operation starts before the temperature of the rotational pressing member is raised sufficiently. Thus, the toner is required to have the low-temperature fixability and a wide range of the offset resistance.
Another configuration in which a heating member is separated from a fixing member and a fixing belt runs between the two members also may be used preferably. The fixing belt may be, e.g., a nickel electroformed belt having heat resistance and deformability or a heat-resistant polyimide belt. Silicone rubber, fluorocarbon rubber, or fluorocarbon resin may be used as a surface coating to improve the releasability.
In the conventional fixing process, release oil has been applied to prevent offset. The toner that exhibits releasability without using oil can eliminate the need for application of the release oil. However, if the release oil is not applied to the fixing means, it can be charged easily. Therefore, when an unfixed toner image is dose to the heating member or the fixing member, the toner may be scattered due to the influence of charge. Such scattering is likely to occur, particularly at low temperature and low humidity.
In contrast, the toner of this embodiment can achieve the low-temperature fixability and a wide range of the offset resistance without using oil. The toner also can provide high color transmittance. Thus, the use of the toner of this embodiment can suppress overcharge as well as scattering caused by the charging action of the heating member or the fixing member
In a 1 liter flask were placed 52 g of phenol, 75 g of formalin (37%), 400 g of spherical magnetite particles with an average particle size of 0.24 μm, 15 g of ammonia water (28%), 1.0 g of calcium fluoride, and 50 g of water, and then the temperature was raised to 85° C. for 60 minutes while stirring the mixture. Subsequently, the mixture was reacted and hardened for 120 minutes at the same temperature, thus producing composite magnetic particles of the phenol resin and the spherical magnetite particles.
After the content of the flask was cooled to 30° C., 0.5 liter of water was added, and the supernatant liquor was removed. The precipitate on the bottom of the flask was washed with water and air-dried. This further was dried at 50° C. to 60° C. under a reduced pressure (5 mmHg or less), so that the composite magnetic particles (carrier core A) were obtained.
In a 1 liter flask were placed 50 g of phenol, 65 g of formalin (37%), 450 g of spherical magnetite particles with an average particle size of 0.24 μm, 15 g of ammonia water (28%), 1.0 g of calcium fluoride, and 50 g of water, and then the temperature was raised to 85° C. for 60 minutes while stirring the mixture. Subsequently, the mixture was reacted and hardened for 120 minutes at the same temperature, thus producing composite magnetic particles of the phenol resin and the spherical magnetite particles.
After the content of the flask was cooled to 30° C., 0.5 liter of water was added, and the supernatant liquor was removed. The precipitate on the bottom of the flask was washed with water and air-dried. This further was dried at 50° C. to 60° C. under a reduced pressure (5 mmHg or less), so that the composite magnetic particles (carrier core B) were obtained.
In a 1 liter flask were placed 47.5 g of phenol, 62 g of formalin (37%), 480 g of spherical magnetite particles with an average particle size of 0.24 μm, 15 g of ammonia water (28%), 1.0 g of calcium fluoride, and 50 g of water, and then the temperature was raised to 85° C. for 60 minutes while stirring the mixture. Subsequently, the mixture was reacted and hardened for 120 minutes at the same temperature, thus producing composite magnetic particles of the phenol resin and the spherical magnetite particles.
After the content of the flask was cooled to 30° C., 0.5 liter of water was added, and the supernatant liquor was removed. The precipitate on the bottom of the flask was washed with water and air-dried. This further was dried at 50° C. to 60° C. under a reduced pressure (5 mmHg or less), so that the composite magnetic particles (carrier core C) were obtained.
A core material d of ferrite particles having an average particle size of 50 μm and a saturation magnetization of 65 Am2/kg in an applied magnetic field of 238.74 kA/m (3000 oersted) was used.
Next, 250 g of polyorganosiloxane expressed as the following Chemical Formula (5) in which R1 and R2 are a methyl group, i.e., (CH3)2SiO2/2 unit is 15.4 mol % and the following Chemical Formula (6) in which R3 is a methyl group, i.e., CH3SiO3/2 unit is 84.6 mol % was allowed to react with 21 g of CF3CH2CH2Si(OCH3)3 to produce a fluorine modified silicone resin. Then, 100 g of the fluorine modified silicone resin (as represented in terms of solid content) and 10 g of aminosilane coupling agent (γ-aminopropyltriethoxysilane) were weighed and dissolved in 300 cc of toluene solvent.
(where R1, R2, R3, and R4 are a methyl group, and m represents a mean degree of polymerization of 100)
(where R1, R2, R3, R4, R5, and R6 are a methyl group, and n represents a mean degree of polymerization of 80)
Using a dip and dry coater, 10 kg of the carrier core A was coated by stirring the resin coating solution for 20 minutes, and then was baked at 260° C. for 1 hour, providing a carrier A1.
The carrier A1 was spherical particles including 80.4 mass % spherical magnetite particles and had an average particle size of 30 μm, a specific gravity of 3.05, a magnetization value of 61 Am2/kg, a volume resistivity of 3×109 Ω·cm, and a specific surface area of 0.098 m2/g.
A carrier B1 was produced in the same manner as the Carrier Producing Example 1 except that the carrier core B was used, and CF3CH2CH2Si(OCH3)3 was changed to C8F17CH2CH2Si(OCH3)3.
The carrier B1 was spherical particles including 88.4 mass % spherical magnetite particles and had an average particle size of 45 μm, a specific gravity of 3.56, a magnetization value of 65 Am2/kg, a volume resistivity of 8×1010 Ω·cm, and a specific surface area of 0.057 m2/g.
A carrier C1 was produced in the same manner as the Carrier Producing Example 1 except that the carrier core C was used, and a conductive carbon (manufactured by Ketjenblack International Corporation EC) was dispersed in an amount of 5 wt % per the resin solid content by using a ball mill.
The carrier C1 was spherical particles including 92.5 mass % spherical magnetite particles and had an average particle size of 48 μm, a specific gravity of 3.98, a magnetization value of 69 Am2/kg, a volume resistivity of 2×107 Ω·cm, and a specific surface area of 0.043 m2/g.
A carrier A2 was produced in the same manner as the Carrier Producing Example 1 except that the amount of aminosilane coupling agent to be added was changed to 30 g.
The carrier A2 was spherical particles including 80.4 mass % spherical magnetite particles and had an average particle size of 30 μm, a specific gravity of 3.05, a magnetization value of 61 Am2/kg, a volume resistivity of 2×1010 Ω·cm, and a specific surface area of 0.01 m2/g.
A core material was produced in the same manner as the Carrier Producing Example 1 except that the amount of aminosilane coupling agent to be added was changed to 50 g, and a coating was applied, thus providing a carrier a1.
As a coating resin, 100 g of straight silicone (SR-2411 manufactured by Dow Corning Toray Silicone Co., Ltd.) was weighed in terms of solid content and dissolved in 300 cc of toluene solvent. Using a dip and dry coater, 10 kg of the ferrite particles d were coated by stirring the resin coating solution for 20 minutes, and then were baked at 210° C. for 1 hour, providing a carrier d2. The carrier d2 had an average particle size of 80 μm, a specific gravity of 5.5, a magnetization value of 75 Am2/kg, a volume resistivity of 2×1012 Ω·cm, and a specific surface area of 0.024 m2/g.
As a coating resin, 100 g of acrylic modified silicone resin (KR-9706 manufactured by Shin-Etsu Chemical Co., Ltd.) was weighed in terms of solid content and dissolved in 300 cc of toluene solvent. Using a dip and dry coater, 10 kg of the ferrite particles d were coated by stirring the resin coating solution for 20 minutes, and then were baked at 210° C. for 1 hour, providing a carrier d3. The carrier d3 had an average particle size of 80 μm, a specific gravity of 5.5, a magnetization value of 75 Am2/kg, a volume resistivity of 2×1011 Ωcm, and a specific surface area of 0.022 m2/g.
Next, examples of the toner of the present invention will be described, but the present invention is not limited by any of the following examples.
Resin Dispersion Production
Table 1 shows the characteristics of the resins used. In Table 1, Mn is a number-average molecular weight, Mw is a weight-average molecular weight, Mz is a Z-average molecular weight, Mp is a peak value of the molecular weight, Tm (° C.) is a softening point, and Tg (° C.) is a glass transition point. Styrene, n-butylacrylate, and acrylic acid are indicated with the mixing amount (g). Table 2 shows the amount of nonion (g) and the amount of anion (g) of the surface-active agents used for each of the resin dispersions, and the ratio of the amount of nonion to the total amount of the surface-active agents.
(1) Resin Particle Dispersion RL1
A monomer solution including 240.1 g of styrene, 59.9 g of n-butylacrylate, and 4.5 g of acrylic acid was dispersed in 440 g of ion-exchanged water with 7.5 g of nonionic surface-active agent (NONIPOL 400 manufactured by Sanyo Chemical Industries, Ltd.), 22.5 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), and 6 g of dodecanethiol. Then, 4.5 g of potassium persulfate was added to the resultant solution, and emulsion polymerization was performed at 75° C. for 4 hours, followed by an aging treatment at 90° C. for 2 hours. Thus, a resin particle dispersion RL1 was prepared, in which the resin particles having Mn of 7200, Mw of 13800, Mz of 20500, Mp of 10800, Tm of 98° C., Tg of 52° C., and a median diameter of 0.14 μm were dispersed. The pH of this resin particle dispersion was 1.8.
(2) Resin Particle Dispersion RL2
A monomer solution including 230.1 g of styrene, 69.9 g of n-butylacrylate, and 4.5 g of acrylic acid was dispersed in 440 g of ion-exchanged water with 7.5 g of nonionic surface-active agent (NONIPOL 400 manufactured by Sanyo Chemical Industries, Ltd.), 22.5 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), and 6 g of dodecanethiol. Then, 4.5 g of potassium persulfate was added to the resultant solution, and emulsion polymerization was performed at 75° C. for 4 hours, followed by an aging treatment at 90° C. for 5 hours. Thus, a resin particle dispersion RL2 was prepared, in which the resin particles having Mn of 7500, Mw of 17600, Mz of 30100, Mp of 18500, Tm of 106° C., Tg of 47° C., and a median diameter of 0.18 μm were dispersed. The pH of this resin particle dispersion was 1.9.
(3) Resin Particle Dispersion RL3
A monomer solution including 230.1 g of styrene, 69.9 g of n-butylacrylate, and 4.5 g of acrylic acid was dispersed in 440 g of ion-exchanged water with 9 g of nonionic surface-active agent (NONIPOL 400 manufactured by Sanyo Chemical Industries, Ltd.), 15 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), and 1.5 g of dodecanethiol. Then, 4.5 g of potassium persulfate was added to the resultant solution, and emulsion polymerization was performed at 75° C. for 4 hours, followed by an aging treatment at 90° C. for 4 hours. Thus, a resin particle dispersion RL2 was prepared, in which the resin particles having Mn of 15300, Mw of 51400, Mz of 87400, Mp of 31400, Tm of 126° C., Tg of 54° C., and a median diameter of 0.18 μm were dispersed. The pH of this resin particle dispersion was 1.8.
(4) Resin Particle Dispersion RH1
A monomer solution including 230.1 g of styrene, 69.9 g of n-butylacrylate, and 4.5 g of acrylic acid was dispersed in 440 g of ion-exchanged water with 6.5 g of nonionic surface-active agent (NONIPOL 400 manufactured by Sanyo Chemical Industries, Ltd.), 27.5 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), and 1.5 g of dodecanethiol. Then, 1.5 g of potassium persulfate was added to the resultant solution, and emulsion polymerization was performed at 75° C. for 4 hours, followed by an aging treatment at 90° C. for 4 hours. Thus, a resin particle dispersion RH1 was prepared, in which the resin particles having Mn of 14300, Mw of 51400, Mz of 189000, Mp of 58000, Tm of 144° C., Tg of 58° C., and a median diameter of 0.14 μm were dispersed. The pH of this resin particle dispersion was 2.0.
(5) Resin Particle Dispersion RH2
A monomer solution including 220 g of styrene, 80 g of n-butylacrylate, and 4.5 g of acrylic acid was dispersed in 440 g of ion-exchanged water with 7.5 g of nonionic surface-active agent (NONIPOL 400 manufactured by Sanyo Chemical Industries, Ltd.) and 22.5 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.). Then, 3 g of potassium persulfate was added to the resultant solution, and emulsion polymerization was performed at 80° C. for 4 hours, followed by an aging treatment at 90° C. for 2 hours. Thus, a resin particle dispersion RH2 was prepared, in which the resin particles having Mn of 23400, Mw of 208500, Mz of 493200, Mp of 89100, Tm of 170° C., Tg of 58° C., and a median diameter of 0.18 μm were dispersed. The pH of this resin particle dispersion was 1.8.
(6) Resin Particle Dispersion rl4
A monomer solution including 240 g of styrene, 60 g of n-butylacrylate, and 4.5 g of acrylic acid was dispersed in 440 g of ion-exchanged water with 6.5 g of nonionic surface-active agent (NONIPOL 400 manufactured by Sanyo Chemical Industries, Ltd.), 27.5 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), 15 g of dodecanethiol, and 3 g of carbon tetrabromide. Then, 3 g of potassium persulfate was added to the resultant solution, and emulsion polymerization was performed at 70° C. for 5 hours, followed by an aging treatment at 80° C. for 2 hours. Thus, a resin particle dispersion rl4 was prepared, in which the resin particles having Mn of 4100, Mw of 7600, Mz of 43000, Mp of 7000, Tm of 89° C., Tg of 39° C., and a median diameter of 0.18 μm were dispersed. The pH of this resin particle dispersion was 1.7.
(7) Resin Particle Dispersion rl5
A monomer solution including 230.1 g of styrene, 69.9 g of n-butylacrylate, and 4.5 g of acrylic acid was dispersed in 440 g of ion-exchanged water with 4.5 g of nonionic surface-active agent (NONIPOL 400 manufactured by Sanyo Chemical Industries, Ltd.), 37.5 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), and 1.5 g of dodecanethiol. Then, 1.5 g of potassium persulfate was added to the resultant solution, and emulsion polymerization was performed at 75° C. for 5 hours, followed by an aging treatment at 80° C. for 2 hours. Thus, a resin particle dispersion rl5 was prepared, in which the resin particles having Mn of 8900, Mw of 61200, Mz of 108400, Mp of 52800, Tm of 142° C., Tg of 57° C., and a median diameter of 0.16 μm were dispersed. The pH of this resin particle dispersion was 1.8.
(8) Resin Particle Dispersion rh3
A monomer solution including 255 g of styrene, 45 g of n-butylacrylate, and 4.5 g of acrylic acid was dispersed in 440 g of ion-exchanged water with 5.5 g of nonionic surface-active agent (NONIPOL 400 manufactured by Sanyo Chemical Industries, Ltd.), 32.5 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), 15 g of dodecanethiol, and 3 g of carbon tetrabromide. Then, 3 g of potassium persulfate was added to the resultant solution, and emulsion polymerization was performed at 75° C. for 5 hours, followed by an aging treatment at 80° C. for 2 hours. Thus, a resin particle dispersion rh3 was prepared, in which the resin particles having Mn of 2600, Mw of 28300, Mz of 96200, Mp of 2700, Tm of 135° C., Tg of 43° C., and a median diameter of 0.18 μm were dispersed. The pH of this resin particle dispersion was 2.0.
(9) Resin Particle Dispersion rh4
A monomer solution including 255 g of styrene, 45 g of n-butylacrylate, and 4.5 g of acrylic acid was dispersed in 350 g of ion-exchanged water with 4.5 g of nonionic surface-active agent (NONIPOL 400 manufactured by Sanyo Chemical Industries, Ltd.) and 37.5 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.). Then, 3 g of potassium persulfate was added to the resultant solution, and emulsion polymerization was performed at 80° C. for 5 hours, followed by an aging treatment at 90° C. for 2 hours. Thus, a resin particle dispersion rh4 was prepared, in which the resin particles having Mn of 18600, Mw of 238700, Mz of 529000, Mp of 163600, Tm of 182° C., Tg of 67° C., and a median diameter of 0.16 μm were dispersed. The pH of this resin particle dispersion was 2.1.
Table 3 shows the pigments used. Table 4 shows the amount of nonion (g) and the amount of anion (g) of the surface-active agents used for each of the pigment dispersions, and the ratio of the amount of nonion to the total amount of the surface-active agents.
(1) Preparation of Colorant Particle Dispersion PM1
20 g of magenta pigment (PERMANENT RUBINE F6B manufactured by Clariant), 2 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), and 78 g of ion-exchanged water were mixed and dispersed by using an ultrasonic dispersing device at an oscillation frequency of 30 kHz for 20 minutes. Thus, a colorant particle dispersion PM1 was prepared, in which the colorant particles having a median diameter of 0.12 μm were dispersed.
(2) Preparation of Colorant Particle Dispersion PC1
20 g of cyan pigment (KETBLUE111 manufactured by Dainippon Ink and Chemicals, Inc.), 2 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), and 78 g of ion-exchanged water were mixed and dispersed by using an ultrasonic dispersing device at an oscillation frequency of 30 kHz for 20 minutes. Thus, a colorant particle dispersion PC1 was prepared, in which the colorant particles having a median diameter of 0.12 μm were dispersed.
(3) Preparation of Colorant Particle Dispersion PY1
20 g of yellow pigment (PY74 manufactured by Sanyo Color Works, Ltd.), 2 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), and 78 g of ion-exchanged water were mixed and dispersed by using an ultrasonic dispersing device at an oscillation frequency of 30 kHz for 20 minutes. Thus, a colorant particle dispersion PY1 was prepared, in which the colorant particles having a median diameter of 0.12 μm were dispersed.
(4) Preparation of Colorant Particle Dispersion PB1
20 g of black pigment (MA100S manufactured by Mitsubishi Chemical Corporation), 2 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), and 78 g of ion-exchanged water were mixed and dispersed by using an ultrasonic dispersing device at an oscillation frequency of 30 kHz for 20 minutes. Thus, a colorant particle dispersion PB1 was prepared, in which the colorant particles having a median diameter of 0.12 μm were dispersed.
(5) Preparation of Colorant Particle Dispersion PM2
20 g of magenta pigment (PERMANENT RUBINE F6B manufactured by Clariant), 1.5 g of nonionic surface-active agent (NONIPOL 400 manufactured by Sanyo Chemical Industries, Ltd.), 6 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), and 78 g of ion-exchanged water were mixed and dispersed by using an ultrasonic dispersing device at an oscillation frequency of 30 kHz for 20 minutes. Thus, a colorant particle dispersion PM2 was prepared, in which the colorant particles having a median diameter of 0.12 g/m were dispersed.
(6) Preparation of Colorant Particle Dispersion pm3
20 g of magenta pigment (PERMANENT RUBINE F6B manufactured by Clariant), 1.2 g of nonionic surface-active agent (NONIPOL 400 manufactured by Sanyo Chemical Industries, Ltd.), 7 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), and 78 g of ion-exchanged water were mixed and dispersed by using an ultrasonic dispersing device at an oscillation frequency of 30 kHz for 20 minutes. Thus, a colorant particle dispersion pm3 was prepared, in which the colorant particles having a median diameter of 0.12 μm were dispersed.
(7) Preparation of Colorant Particle Dispersion pm4
20 g of magenta pigment (PERMANENT RUBINE F6B manufactured by Clariant), 10 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), and 78 g of ion-exchanged water were mixed and dispersed by using an ultrasonic dispersing device at an oscillation frequency of 30 kHz for 20 minutes. Thus, a colorant particle dispersion pm4 was prepared, in which the colorant particles having a median diameter of 0.12 μm were dispersed.
Tables 5, 6, 7 and 8 show the characteristics of the waxes used.
Tmw (° C.) is a melting point, and Ck (wt %) is a heating loss. PR16 is 16% diameter, PR50 is 50% diameter, and PR84 is 84% diameter in the cumulative volume particle size distribution obtained by accumulation from the smaller particle diameter side. In Table 8, the values in parentheses indicate the mixing ratio of the waxes. Table 9 shows the amount of nonion (g) and the amount of anion (g) of the surface-active agents used for each of the wax dispersions, and the ratio of the amount of nonion to the total amount of the surface-active agents.
(1) Preparation of Wax Particle Dispersion WA1
The tank was kept at atmospheric pressure, and 67 g of ion-exchanged water, 2 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 5 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), 5 g of the first wax (W-1), and 25 g of the second wax (W-11) were blended and treated while the rotating body rotated at a rotational speed of 30 m/s for 5 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion WA1 was provided.
(2) Preparation of Wax Particle Dispersion WA2
Under the same conditions as the preparation (1) except that the tank was pressurized at 0.4 Mpa, 67 g of ion-exchanged water, 1.8 g of nonionic surface-active agent (ELEMTNOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 6 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), 10 g of the first wax (W-2), and 20 g of the second wax (W-12) were blended and treated while the rotating body rotated at a rotational speed of 30 mls for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion WA2 was provided.
(3) Preparation of Wax Particle Dispersion WA3
Under the same conditions as the preparation (1) except that the tank was pressurized at 0.4 Mpa, 67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 15 g of the first wax (W-3), and 15 g of the second wax (W-13) were blended and treated while the rotating body rotated at a rotational speed of 20 m/s for 3 minutes, and then 45 m/s for 2 minutes. Thus, a wax particle dispersion WA3 was provided.
(4) Preparation of Wax Particle Dispersion WA4
Under the same conditions as the preparation (1), 67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 10 g of the first wax (W-4), and 20 g of the second wax (W-11) were blended and treated while the rotating body rotated at a rotational speed of 30 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion WA4 was provided.
(5) Preparation of Wax Particle Dispersion WA5
The material liquid, in which wax and a surface-active agent were predispersed in a pressurized and heated aqueous medium, was introduced from the inlet 850 and treated instantaneously to make a fine particle dispersion. The amount of material liquid supplied was 1 kg/h, and the maximum rotational speed of the rotor 853 was 100 m/s.
67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 6 g of the first wax (W-5), and 24 g of the second wax (W-12) were blended and treated in a supplied amount of 1 kg/h while the rotor rotated at a rotational speed of 100 m/s. Thus, a wax particle dispersion WA5 was provided.
(6) Preparation of Wax Particle Dispersion WA6
Under the same conditions as the preparation (1), 67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 5 g of the first wax (W-6), and 25 g of the second wax (W-11) were blended and treated while the rotating body rotated at a rotational speed of 20 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion WA6 was provided.
(7) Preparation of Wax Particle Dispersion WA7
Under the same conditions as the preparation (1), 67 g of ion-exchanged water, 1.8 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 6 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), 5 g of the first wax (W-6), and 25 g of the second wax (W-11) were blended and treated while the rotating body rotated at a rotational speed of 20 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion WA7 was provided.
(8) Preparation of Wax Particle Dispersion WA8
Under the same conditions as the preparation (1) except that the tank was pressurized at 0.4 Mpa, 67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 7.5 g of the first wax (W-7), and 22.5 g of the second wax (W-12) were blended and treated while the rotating body rotated at a rotational speed of 20 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion WA8 was provided.
(9) Preparation of Wax Particle Dispersion WA9
Under the same conditions as the preparation (5), 67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 15 g of the first wax (W-8), and 15 g of the second wax (W-13) were blended and treated in a supplied amount of 1 kg/h while the rotor rotated at a rotational speed of 100 m/s. Thus, a wax particle dispersion WA9 was provided.
(10) Preparation of Wax Particle Dispersion WA10
Under the same conditions as the preparation (1), 67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 15 g of the first wax (W-9), and 15 g of the second wax (W-11) were blended and treated while the rotating body rotated at a rotational speed of 20 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion WA9 was provided.
(11) Preparation of Wax Particle Dispersion WA11
Under the same conditions as the preparation (1) except that the tank was pressurized at 0.4 Mpa, 67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 10 g of the first wax (W-10), and 20 g of the second wax (W-12) were blended and treated while the rotating body rotated at a rotational speed of 30 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion WA11 was provided.
(12) Preparation of Wax Particle Dispersion WA12
Under the same conditions as the preparation (1), 67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), and 30 g of the first wax (W-1) were blended and treated while the rotating body rotated at a rotational speed of 20 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion WA12 was provided.
(13) Preparation of Wax Particle Dispersion WA13
Under the same conditions as the preparation (1), 67 g of ion-exchanged water, 1.8 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 6 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), and 30 g of the first wax (W-2) were blended and treated while the rotating body rotated at a rotational speed of 30 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion WA13 was provided.
(14) Preparation of Wax Particle Dispersion WA14
Under the same conditions as the preparation (5), 67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), and 30 g of the first wax (W-3) were blended and treated in a supplied amount of 1 kg/h while the rotor rotated at a rotational speed of 100 m/s. Thus, a wax particle dispersion WA14 was provided.
(15) Preparation of Wax Particle Dispersion WA15
Under the same conditions as the preparation (1), 67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), and 30 g of the first wax (W-6) were blended and treated while the rotating body rotated at a rotational speed of 20 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion WA15 was provided.
(16) Preparation of Wax Particle Dispersion WA11
Under the same conditions as the preparation (1) except that the tank was pressurized at 0.4 Mpa, 67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), and 30 g of the first wax (W-11) were blended and treated while the rotating body rotated at a rotational speed of 20 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion WA16 was provided.
(17) Preparation of Wax Particle Dispersion WA17
Under the same conditions as the preparation (1) except that the tank was pressurized at 0.4 Mpa, 67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), and 30 g of the first wax (W-12) were blended and treated while the rotating body rotated at a rotational speed of 20 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion WA17 was provided.
(18) Preparation of Wax Particle Dispersion WA18
Under the same conditions as the preparation (1) except that the tank was pressurized at 0.4 Mpa, 67 g of ion-exchanged water, 3 g of nonionic surface-active agent ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), and 30 g of the first wax (W-13) were blended and treated in a supplied amount of 1 kg/h while the rotor rotated at a rotational speed of 100 m/s. Thus, a wax particle dispersion WA18 was provided.
(19) Preparation of Wax Particle Dispersion wa21
Under the same conditions as the preparation (4), 67 g of ion-exchanged water, 3 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 18 g of the first wax (W-4), and 12 g of the second wax (W-11) were blended and treated while the rotating body rotated at a rotational speed of 30 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion wa21 was provided.
(20) Preparation of Wax Particle Dispersion wa22
Under the same conditions as the preparation (6), 67 g of ion-exchanged water, 1.4 g of nonionic surface-active agent (ELEMINOL NA 400 manufactured by Sanyo Chemical Industries, Ltd.), 8 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), 5 g of the first wax (W-6), and 25 g of the second wax (W-11) were blended and treated while the rotating body rotated at a rotational speed of 20 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion wa22 was provided.
(21) Preparation of Wax Particle Dispersion wa23
Under the same conditions as the preparation (6), 67 g of ion-exchanged water, 15 g of anionic surface-active agent (S20-F, a 20% concentration aqueous solution, manufactured by Sanyo Chemical Industries, Ltd.), 5 g of the first wax (W-6), and 25 g of the second wax (W-11) were blended and treated while the rotating body rotated at a rotational speed of 20 m/s for 3 minutes, and then 50 m/s for 2 minutes. Thus, a wax particle dispersion wa23 was provided.
Tables 10 and 11 show the compositions and the characteristics of the toners produced, respectively. In Tables 10 and 11, d50 (μm) is a volume-average particle size of the toner base particles, 2.52-4 (pop %) is the content (%) of toner particles having a particle size of 2.52 to 4 μm in a number distribution, V46:4-6.06 (vol %) is the content (%) of toner particles having a particle size of 4 to 6.06 μm in a volume distribution, P46:4-6.06 (pop %) is the content (%) of toner particles having a particle size of 4 to 6.06 μm in the number distribution, and over 8 μm (vol %) is the content (%) of toner particles having a particle size of 8 μm or more in the volume distribution.
(1) Preparation of Toner Base M1
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL1, 45 g of colorant particle dispersion PM1, 85 g of wax particle dispersion WA1, and 500 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T25 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 3.5.
Then, the pH was increased to 11.8 by adding 1N NaOH to the mixed dispersion. Subsequently, 317 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.2.
Moreover, the water temperature was kept at 90° C., and then 165 g of second resin particle dispersion RH 1 with an adjusted pH of 8.5 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 90° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M1 with a volume-average particle size of 4.1 μm and a coefficient of variation of 18.7.
If the pH before adding the water-soluble inorganic salt and heating was less than 9.5, the core particles became coarser to the extent that the volume-average particle size was 15 μm or more. If the pH was 12.5, the amount of liberated wax was increased, and it was difficult to incorporate the wax uniformly. The mixed dispersion remained white and cloudy.
If the pH of the mixed dispersion at the time of forming the core particles was more than 9.5, the numbers of liberated wax or colorant particles were increased due to poor aggregation.
(2) Preparation of Toner Base M2
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL1, 31 g of colorant particle dispersion PM1, 40 g of wax particle dispersion WA3, and 330 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T25 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 3.8.
Then, the pH was increased to 11.1 by adding 1N NaOH to the mixed dispersion. Subsequently, 261 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 8.5.
Moreover, the water temperature was kept at 90° C., and then 50 g of second resin particle dispersion RH2 with an adjusted pH of 7.5 was added at a drop rate of 1 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 2 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M2d with a volume-average particle size of 4.6 μm and a coefficient of variation of 17.1.
Table 12 shows changes in the temperature inside of a container, the pH of the liquid, and the volume-average particle size (d50 (μm)) with time in each of the core particle formation process after mixing the first resin, colorant, and wax particle dispersions and the second resin particle fusion process after dropping the second resin particle dispersion. The “R: (figure)” in the column referred to as “at the time of completion of the dropping” indicates the adjusted pH of the second resin particle dispersion. M2a to M2j correspond to the adjusted pH values of 10.5, 9.5, 8.5, 7.5, 6.5, 5.5, 4.5, 3.5, 2.5 and 11 of the second resin particle dispersion, respectively. Table 12 also shows the volume-average particle size and the shape factor at 2 hours after completion of dropping.
When the pH was adjusted from 7.5 to 10.5, the particles tended to be irregular in shape. At the pH of 2.5, while the second resin particle dispersion was dropped, the second resin particles did not adhere to the core particles at all. Therefore, only the second resin particles were aggregated, resulting in a considerably broader particle size distribution in which the coefficient of variation in volume was 40 or more. The dispersion remained white and cloudy.
When the second resin particle dispersion was dropped after adjusting the pH to 3.2, the second resin particles did not adhere easily to the core particles. Thus, the fusion of the second resin particles with the core particle took 5 hours or more. In this case, the coefficient of variation in volume was 32, and the particle size distribution was considerably broader. At the pH of 11, the particles produced became coarser to have a volume-average particle size of 12 μm or more.
Using Real Surface View Microscope (VE7800) manufactured by KEYENCE CORPORATION, the toner base (also referred to as colored particles) was magnified by 1000 times, and about 100 particles were taken to measure the circumference and the cross-sectional area. The shape factor (KC) was determined by the following formula.
KC(shape factor)=d2/(4π·A)×100
where d is a circumference of the toner base, and A is a cross-sectional area of the toner base.
(3) Preparation of Toner Base M3 In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL1, 31 g of colorant particle dispersion PM1, 40 g of wax particle dispersion WA4, and 330 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T25 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 3.8.
Then, the pH was increased to 11.9 by adding 1N NaOH to the mixed dispersion. Subsequently, 261 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.3.
Moreover, the water temperature was kept at 90° C., and then 50 g of second resin particle dispersion RH2 with an adjusted pH of 6.5 was added at a drop rate of 1 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 2 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M3e with a volume-average particle size of 4.1 μm and a coefficient of variation of 16.4. Table 13 shows changes in the temperature inside of a container, the pH of the liquid, and the volume-average particle size (d50 (μm)) with time in each of the core particle formation process after mixing the first resin, colorant, and wax particle dispersions and the second resin particle fusion process after dropping the second resin particle dispersion. The “R: (figure)” in the column referred to as “at the time of completion of the dropping” indicates the adjusted pH of the second resin particle dispersion. M3a to M3i correspond to the adjusted pH values of 10.5, 9.5, 8.5, 7.5, 6.5, 5.5, 4.5, 3.5 and 11 of the second resin particle dispersion, respectively, Table 13 also shows the volume-average particle size and the shape factor at 2 hours after completion of dropping.
When the pH was adjusted from 8.5 to 10.5, the particles tended to be irregular in shape.
At the pH of 3.5, while the second resin particle dispersion was dropped, the second resin particles did not adhere to the core particles at all. Therefore, only the second resin particles were aggregated, resulting in a considerably broader particle size distribution in which the coefficient of variation in volume was 40 or more. The dispersion remained white and cloudy. At the pH of 11 the particles produced became coarser to have a volume-average particle size of 15 μm or more.
(4) Preparation of Toner Base M4
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 42 g of colorant particle dispersion PM1, 90 g of wax particle dispersion WA5, and 500 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T50 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 2.2.
Then, the pH was increased to 9.7 by adding 1N NaOH to the mixed dispersion. Subsequently, 319 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 7.
Moreover, the water temperature was kept at 90° C., and then 145 g of second resin particle dispersion RH1 with an adjusted pH of 5 was added at a drop rate of 10 g/min. After completion of the dropping, this mixture was heat-treated at 90° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M4e with a volume-average particle size of 6.2 μm and a coefficient of variation of 17.1.
Table 14 shows changes in the temperature inside of a container, the pH of the liquid, and the volume-average particle size (d50 (μm)) with time in each of the core particle formation process after mixing the first resin, colorant, and wax particle dispersions and the second resin particle fusion process after dropping the second resin particle dispersion. The “R: (figure)” in the column referred to as “at the time of completion of the dropping” indicates the adjusted pH of the second resin particle dispersion. M4a to M4h correspond to the adjusted pH values of 9, 8, 7, 6, 5, 4, 2.5 and 11 of the second resin particle dispersion, respectively. Table 14 also shows the volume-average particle size and the shape factor at 1.5 hours after completion of dropping.
When the pH was adjusted from 6 to 9, the particles tended to be irregular in shape.
At the pH of 2.5, while the second resin particle dispersion was dropped, the second resin particles did not adhere to the core particles at all. Therefore, only the second resin particles were aggregated, resulting in a considerably broader particle size distribution in which the coefficient of variation in volume was 40 or more. The dispersion remained white and cloudy. At the pH of 11, the particles produced became coarser to have a volume-average particle size of 15 μm or more.
(5) Preparation of Toner Base M5
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 42 g of colorant particle dispersion PM1, 50 g of wax particle dispersion WA6, and 450 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T50 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 3.8.
Then, the pH was increased to 11.8 by adding 1N NaOH to the mixed dispersion. Subsequently 281 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.2.
Moreover, the water temperature was kept at 90° C., and then 145 g of second resin particle dispersion RH1 with an adjusted pH of 5 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M5 with a volume-average particle size of 4.2 μm and a coefficient of variation of 18.9.
(6) Preparation of Toner Base M6
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 42 g of colorant particle dispersion PM1, 50 g of wax particle dispersion WA7, and 450 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T50 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 2.9.
Then, the pH was increased to 11.7 by adding 1N NaOH to the mixed dispersion. Subsequently, 281 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.2.
Moreover, the water temperature was kept at 90° C., and then 145 g of second resin particle dispersion RH1 with an adjusted pH of 5 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base MG with a volume-average particle size of 4.5 μm and a coefficient of variation of 19.8.
(7) Preparation of Toner Base M7
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 32 g of colorant particle dispersion PM1, 60 g of wax particle dispersion WA8, and 360 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T25 manufactured by IKA CO., LTD.) Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 1.8.
Then, the pH was increased to 9.7 by adding 1N NaOH to the mixed dispersion. Subsequently, 281 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 906C at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 7.2.
Moreover, the water temperature was kept at 90° C., and then 60 g of second resin particle dispersion RH2 with an adjusted pH of 4.5 was added at a drop rate of 10 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 2 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M7 with a volume-average particle size of 5.9 μm and a coefficient of variation of 19.1.
(8) Preparation of Toner Base M8
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 32 g of colorant particle dispersion PM1, 40 g of wax particle dispersion WA9, and 350 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T25 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 2.1.
Then, the pH was increased to 11.2 by adding 1N NaOH to the mixed dispersion. Subsequently, 262 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 8.5.
Moreover, the water temperature was kept at 90° C., and then 60 g of second resin particle dispersion RH2 with an adjusted pH of 8 was added at a drop rate of 1 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 2 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M8 with a volume-average particle size of 5 μm and a coefficient of variation of 16.2.
(9) Preparation of Toner Base M9
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL3, 45 g of colorant particle dispersion PM1, 90 g of wax particle dispersion WA10, and 500 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T50 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 2.8.
Then, the pH was increased to 11.9 by adding 1N NaOH to the mixed dispersion. Subsequently, 322 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.3.
Moreover, the water temperature was kept at 90° C., and then 165 g of second resin particle dispersion RH1 with an adjusted pH of 6 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 90° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M9 with a volume-average particle size of 4.1 μm and a coefficient of variation of 16.1.
(10) Preparation of Toner Base M10
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 42 g of colorant particle dispersion PM2, 50 g of wax particle dispersion WA7, and 450 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T50 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 2.6.
Then, the pH was increased to 11.7 by adding 1N NaOH to the mixed dispersion. Subsequently, 281 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.2.
Moreover, the water temperature was kept at 90° C., and then 145 g of second resin particle dispersion RH1 with an adjusted pH of 5 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M10 with a volume-average particle size of 4.8 μm and a coefficient of variation of 20.1.
(11) Preparation of Toner Base M11
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 45 g of colorant particle dispersion PM1, 50 g of wax particle dispersion WA11, and 450 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T25 manufactured by IKA CO., LTD.) Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 2.5.
Then, the pH was increased to 11.8 by adding 1N NaOH to the mixed dispersion. Subsequently, 284 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.2.
Moreover, the water temperature was kept at 90° C., and then 165 g of second resin particle dispersion RH2 with an adjusted pH of 8.8 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 90° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M11 with a volume-average particle size of 4.1 μm and a coefficient of variation of 18.6.
In this case, when the second resin particle dispersion was dropped after adjusting the pH to 9.7, the core particles were significantly aggregated together, so that the particles produced became coarser to have a volume-average particle size of 14 μm or more.
(12) Preparation of Toner Base M12
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 45 g of colorant particle dispersion PM1, 50 g of wax particle dispersion WA12, and 450 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T25 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 1.8.
Then, the pH was increased to 9.7 by adding 1N NaOH to the mixed dispersion. Subsequently, 284 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 7.2.
Moreover, the water temperature was kept at 90° C., and then 165 g of second resin particle dispersion RH2 with an adjusted pH of 4 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 90° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M12 with a volume-average particle size of 5.8 μm and a coefficient of variation of 17.1.
(13) Preparation of Toner Base M13
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 37 g of colorant particle dispersion PM1, 85 g of wax particle dispersion WA13, and 400 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T25 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 2.8.
Then, the pH was increased to 11 by adding 1N NaOH to the mixed dispersion. Subsequently, 310 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 8.4.
Moreover, the water temperature was kept at 90° C., and then 100 g of second resin particle dispersion RH2 with an adjusted pH of 8.0 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 90° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M13 with a volume-average particle size of 5.4 μm and a coefficient of variation of 19.8.
(14) Preparation of Toner Base M14
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 37 g of colorant particle dispersion PM1, 85 g of wax particle dispersion WA14, and 400 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T25 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 2.8.
Then, the pH was increased to 11.9 by adding 1N NaOH to the mixed dispersion. Subsequently, 310 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.3.
Moreover, the water temperature was kept at 90° C., and then 100 g of second resin particle dispersion RH2 with an adjusted pH of 9.1 was added at a drop rate of 1 g/min. After completion of the dropping, this mixture was heat-treated at 90° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M14 with a volume-average particle size of 3.8 μm and a coefficient of variation of 21.8.
(15) Preparation of Toner Base M15
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL1, 42 g of colorant particle dispersion PM1, 65 g of wax p article dispersion WA15, and 450 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T50 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 2.2.
Then, the pH was increased to 9.7 by adding 1N NaOH to the mixed dispersion. Subsequently, 295 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 7.
Moreover, the water temperature was kept at 90° C., and then 145 g of second resin particle dispersion RH1 with an adjusted pH of 3.8 was added at a drop rate of 10 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 2 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M15 with a volume-average particle size of 6.4 μm and a coefficient of variation of 18.8.
(16) Preparation of Toner Base M16
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL1, 42 g of colorant particle dispersion PM1, 65 g of wax particle dispersion WA16, and 450 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T50 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 2.3.
Then, the pH was increased to 11.8 by adding 1N NaOH to the mixed dispersion. Subsequently, 295 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.2.
Moreover, the water temperature was kept at 90° C., and then 145 g of second resin particle dispersion RH1 with an adjusted pH of 5 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 2 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base M16 with a volume-average particle size of 4.2 μm and a coefficient of variation of 16.2.
(17) Preparation of Toner Base m21
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL1, 31 g of colorant particle dispersion PM1, 40 g of wax particle dispersion wa12, and 330 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T25 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 2.8.
Then, the pH was increased to 11.7 by adding 1N NaOH to the mixed dispersion. Subsequently, 261 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.1.
Moreover, the water temperature was kept at 90° C., and then 50 g of second resin particle dispersion RH2 with an adjusted pH of 6.5 was added at a drop rate of 1 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 2 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base m21 with a volume-average particle size of 7.4 μm and a coefficient of variation of 23.8. In the toner base m21, the particle size distribution became slightly broader.
(18) Preparation of Toner Base m22
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 42 g of colorant particle dispersion PM1, 50 g of wax particle dispersion wa13, and 450 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T50 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 2.8.
Then, the pH was increased to 11.8 by adding 1N NaOH to the mixed dispersion. Subsequently, 281 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.2.
Moreover, the water temperature was kept at 90° C., and then 145 g of second resin particle dispersion RH1 with an adjusted pH of 5 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base m22 with a volume-average particle size of 8.4 μm and a coefficient of variation of 24.8. In the toner base m22, the particle size distribution became slightly broader, and part of the aqueous medium remained white and cloudy.
(19) Preparation of Toner Base m23
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 42 g of colorant p article dispersion PM1, 50 g of wax particle dispersion wa14, and 450 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T50 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 3.8.
Then, the pH was increased to 11.8 by adding 1N NaOH to the mixed dispersion. Subsequently, 281 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.2.
Moreover, the water temperature was kept at 90° C., and then 145 g of second resin particle dispersion RH1 with an adjusted pH of 5 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base m23 with a volume-average particle size of 10.8 μm and a coefficient of variation of 31.8. In the toner base m23, the particle size distribution became broader, and part of the aqueous medium remained white and cloudy.
(20) Preparation of Toner Base m24
In a 2000 ml four-neck flask equipped with a thermometer and a cooling tube were placed 204 g of first resin particle dispersion rl5, 32 g of colorant particle dispersion PM1, 40 g of wax particle dispersion WA2, and 350 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T25 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 3.9.
Then, the pH was increased to 11.8 by adding 1N NaOH to the mixed dispersion. Subsequently, 262 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.0.
Moreover, the water temperature was kept at 90° C., and then 60 g of second resin particle dispersion RH2 with an adjusted pH of 7.5 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 2 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base m24 with a volume-average particle size of 3.9 μm and a coefficient of variation of 35.8. In the toner base m24, the particle size distribution became broader
(21) Preparation of Toner Base m25
In a 2000 ml four-neck flask equipped with a thermometer and a cooling tube were placed 204 g of first resin particle dispersion rl4, 45 g of colorant particle dispersion PM1, 50 g of wax particle dispersion WA6, and 450 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T25 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 3.9. Then, the pH was increased to 9.7 by adding 1N NaOH to the mixed dispersion. Subsequently, 284 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 7.
Moreover, the water temperature was kept at 90° C., and then 165 g of second resin particle dispersion rh3 with an adjusted pH of 6.5 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 90° C. for 2 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base m25 with a volume-average particle size of 15.3 μm and a coefficient of variation of 32.5. In the toner base m25, the particle size distribution became broader.
(22) Preparation of Toner Base m26 In a 2000 ml four-neck flask equipped with a thermometer and a cooling tube were placed 204 g of first resin particle dispersion rl5, 34 g of colorant particle dispersion PM1, 40 g of wax particle dispersion WA7, and 350 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T25 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 4.1. Then, the pH was increased to 11.4 by adding 1N NaOH to the mixed dispersion. Subsequently, 264 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.1.
Moreover, the water temperature was kept at 90° C., and then 75 g of second resin particle dispersion rh4 with an adjusted pH of 7.0 was added at a drop rate of 1 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 2 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base m26 with a volume-average particle size of 4.9 μm and a coefficient of variation of 37.6. In the toner base m26, the particle size distribution became broader.
(23) Preparation of Toner Base m27
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 42 g of colorant particle dispersion pm3, 50 g of wax particle dispersion WA7, and 450 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T50 manufactured by IKA CO., LTD.)) Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 3.2.
Then, the pH was increased to 11.7 by adding 1N NaOH to the mixed dispersion. Subsequently, 281 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.2.
Moreover, the water temperature was kept at 90° C., and then 145 g of second resin particle dispersion RH1 with an adjusted pH of 5 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base m27 with a volume-average particle size of 8.2 μm and a coefficient of variation of 26.8. In the toner base m27, the particle size distribution became slightly broader.
(24) Preparation of Toner Base m28
In a 2000 ml four-neck flask equipped with a thermometer, a cooling tube, a stirring rod, and a pH meter were placed 204 g of first resin particle dispersion RL2, 42 g of colorant particle dispersion pm4, 50 g of wax particle dispersion WA7, and 450 ml of ion-exchanged water, and then mixed for 10 minutes by using a homogenizer (Ultratalax T50 manufactured by IKA CO., LTD.). Thus, a mixed dispersion was prepared. The pH of the mixed dispersion was 3.2.
Then, the pH was increased to 11.7 by adding 1N NaOH to the mixed dispersion. Subsequently, 281 g of magnesium sulfate aqueous solution (23% concentration) was added and stirred for 10 minutes. After the temperature was raised from 20° C. to 90° C. at a rate of 1° C./min, the mixture was heat-treated for 3 hours, thus forming core particles. The pH of the core particle dispersion was 9.2.
Moreover, the water temperature was kept at 90° C., and then 145 g of second resin particle dispersion RH1 with an adjusted pH of 5 was added at a drop rate of 5 g/min. After completion of the dropping, this mixture was heat-treated at 95° C. for 1.5 hours, thereby providing particles fused with the second resin particles.
After cooling, the reaction product (toner base) was filtered and washed three times with ion-exchanged water. The toner base thus obtained was dried at 40° C. for 6 hours by using a fluid-type dryer, resulting in a toner base m28 with a volume-average particle size of 12.1 μm and a coefficient of variation of 32.6. In the toner base m28, the particle size distribution became broader.
Table 15 shows the additives used in this example. The charge amount was measured by a blow-off method using frictional charge with an uncoated ferrite carrier. Under the environmental conditions of 25° C. and 45% RH, 50 g of carrier and 0.1 g of silica or the like were mixed in a 100 ml polyethylene container, and then stirred by vertical rotation at a speed of 100 min−1 for 5 minutes and 30 minutes, respectively. Thereafter, 0.3 g of sample was taken for each stirring time, and a nitrogen gas was blown on the samples at 1.96×104 (Pa) for 1 minute. The mixing weight ratio of the treatment materials A and B is shown in parentheses.
It is preferable that the 5-minute value is −100 to −800 μC/g and the 30-minute value is −50 to −600 μC/g for the negative chargeability. Silica having a high charge amount can function well in a small quantity.
Table 16 shows the toner material compositions used in this example. The compositions of black, cyan, and yellow toners were the same as the composition of a magenta toner except that PB1, PC1, and PY1 were used as pigments, respectively.
In each of the additives, the values in parentheses indicate the amount (parts by weight) of the additive per 100 parts by weight of the toner base. The addition treatment was performed by using a Henschel mixer FM20B (manufactured by Mitsui Mining Co., Ltd.) with a Z0S0-type mixer blade, an input amount of 1 kg, a number of revolutions of 2000 min−1, and a treating time of 5 minutes.
The transfer belt 12 can be obtained by kneading a conductive filler in an insulating resin and making a film with an extruder. In this example, polycarbonate resin (e.g., European Z300 manufactured by Mitsubishi Gas Kagaku Co., Ltd.) was used as the insulating resin, and 5 parts by weight of conductive carbon (e.g., “KETJENBLACK”) were added to 95 parts by weight of the polycarbonate resin to form a film. The surface of the film was coated with a fluorocarbon resin. The film had a thickness of about 100 g/m, a volume resistance of 107 to 1012 Ω·cm, and a surface resistance of 107 to 1012 Ω/□ (square). The use of this film can improve the dot reproducibility and prevent slackening of the transfer belt 12 over a long period of use and charge accumulation effectively. By coating the film surface with a fluorocarbon resin, the filming of toner on the surface of the transfer belt 12 due to a long period of use also can be suppressed effectively. If the volume resistance is less than 107 Ω·cm, retransfer is likely to occur. If the volume resistance is more than 1012 Ω·cm, the transfer efficiency is degraded.
A first transfer roller 10 is a conductive polyurethane foam including carbon black and has an outer diameter of 8 mm. The resistance value is 102 to 106Ω. In the first transfer operation, the first transfer roller 10 is pressed against a photoconductive member 1 with a force of about 1.0 to 9.8 (N) via the transfer belt 12, so that the toner is transferred from the photoconductive member 1 to the transfer belt 12. If the resistance value is less than 102Ω, retransfer is likely to occur. If the resistance value is more than 106Ω, a transfer failure is likely to occur. The force less than 1.0 (N) may cause a transfer failure, and the force more than 9.8 (N) may cause transfer voids.
The second transfer roller 14 is a conductive polyurethane foam including carbon black and has an outer diameter of 10 mm. The resistance value is 102 to 106Ω. The second transfer roller 14 is pressed against the follower roller 13 via the transfer belt 12 and a transfer medium 19 such as a paper or OHP sheet. The follower roller 13 is rotated in accordance with the movement of the transfer belt 12. In the second transfer operation, the second transfer roller 14 is pressed against the follower roller 13 with a force of 5.0 to 21.8 (N), so that the toner is transferred from the transfer belt 12 to the transfer medium 19. If the resistance value is less than 102Ω, retransfer is likely to occur. If the resistance value is more than 106Ω, a transfer failure is likely to occur. The force less than 5.0 (N) may cause a transfer failure, and the force more than 21.8 (N) may increase the load and generate jitter easily.
Four image forming units 18Y, 18M, 18C, and 18K for yellow (Y), magenta (M), cyan (C), and black (K) are arranged in series, as shown in
The image forming units 18Y, 18M, 18C, and 18K have the same components except for a developer contained therein. For simplification, only the image forming unit 18Y for yellow (Y) will be described, and an explanation of the other units will not be repeated.
The image forming unit is configured as follows. Reference numeral 1 is a photoconductive member, 3 is pixel laser signal light, and 4 is a developing roller of aluminum that has an outer diameter of 10 mm and includes a magnet with a magnetic force of 1200 gauss. The developing roller 4 is located opposite to the photoconductive member 1 with a gap of 0.3 mm between them, and rotates in the direction of the arrow. A stirring roller 6 stirs toner and a carrier in a developing unit and supplies the toner to the developing roller 4. The mixing ratio of the toner to the carrier is read from a permeability sensor (not shown), and the toner is supplied timely from a toner hopper (not shown). A magnetic blade 5 is made of metal and controls a magnetic brush layer of a developer on the developing roller 4. In this example, 150 g of developer was introduced, and the gap was 0.4 mm. Although a power supply is not shown in
A charging roller 2 is made of epichlorohydrin rubber and has an outer diameter of 10 mm. A direct-current bias of −1.2 kV is applied to the charging roller 2 for charging the surface of the photoconductive member 1 to −600 V Reference numeral 8 is a cleaner, 9 is a waste toner box, and 7 is a developer.
A paper is conveyed from the lower side of the transfer belt unit 17, and a paper conveying path is formed so that a paper 19 is transported by a paper feed roller (not shown) to a nip portion where the transfer belt 12 and the second transfer roller 14 are pressed against each other.
The toner is transferred from the transfer belt 12 to the paper 19 by +1000 V applied to the second transfer roller 14, and then is conveyed to a fixing portion in which the toner is fixed. The fixing portion includes a fixing roller 201, a pressure roller 202, a fixing belt 203, a heat roller 204, and an induction heater 205.
The belt 203 is formed by arranging a Ni substrate (30 μm), silicone rubber (150 μm), and PFA (tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer) (30 μm) in layers.
The pressure roller 202 is pressed against the fixing roller 201 by a spring 209. A recording material 19 with the toner 210 is moved along a guide plate 211.
The fixing roller 201 fixing member) includes a hollow core 213, an elastic layer 214 formed on the hollow core 213, and a silicone rubber layer 215 formed on the elastic layer 214. The hollow core 213 is made of aluminum and has a length of 250 mm, an outer diameter of 14 mm, and a thickness of 1 mm. The elastic layer 214 is made of silicone rubber with a rubber hardness (JIS-A) of 20 degrees based on the JIS standard and has a thickness of 3 mm. The silicone rubber layer 215 has a thickness of 3 mm. Therefore, the outer diameter of the fixing roller 201 is about 26 mm. The fixing roller 201 is rotated at 125 mm/s with a driving force from a driving motor (not shown).
The heat roller 204 includes a hollow pipe having a thickness of 1 mm and an outer diameter of 20 mm. The surface temperature of the fixing belt is controlled to 170° C. with a thermistor.
The pressure roller 202 (pressure member) has a length of 250 mm and an outer diameter of 20 mm, and includes a hollow core 216 and an elastic layer 217 formed on the hollow core 216. The hollow core 216 is made of aluminum and has an outer diameter of 16 mm and a thickness of 1 mm. The elastic layer 217 is made of silicone rubber with a rubber hardness (JIS-A) of 55 degrees based on the JIS standard and has a thickness of 2 mm. The pressure roller 202 is mounted rotatably, and a 5.0 mm width nip is formed between the pressure roller 202 and the fixing roller 201 under a one-sided load of 147N from the spring 209.
The operations will be described below. In the full color mode, all the first transfer rollers 10 of Y, M, C, and K are lifted and pressed against the respective photoconductive members 1 of the image forming units via the transfer belt 12. At this time, a direct-current bias of +800 V is applied to each of the first transfer rollers 10. An image signal is transmitted through the laser beam 3 and enters the photoconductive member 1 whose surface has been charged by the charging roller 2, thus forming an electrostatic latent image. The electrostatic latent image formed on the photoconductive member 1 is made visible by the toner on the developing roller 4 that is rotated in contact with the photoconductive member 1.
In this case, the image formation rate (125 mm/s, which is equal to the circumferential velocity of the photoconductive member) of the image forming unit 18Y is set so that the speed of the photoconductive member is 0.5 to 1.5% slower than the traveling speed of the transfer belt 12.
In the image forming process, signal light 3Y is input to the image forming unit 18Y, and an image is formed with Y toner. At the same time as the image formation, the Y toner image is transferred from the photoconductive member 1Y to the transfer belt 12 by the action of the first transfer roller 10Y, to which a direct voltage of +800 V is applied. There is a time lag between the first transfer of the first color (Y) and the first transfer of the second color (M). Then, signal light 3M is input to the image forming unit 18M, and an image is formed with M toner. At the same time as the image formation, the M toner image is transferred from the photoconductive member 1M to the transfer belt 12 by the action of the first transfer roller 10M. In this case, the M toner is transferred onto the first color (Y) toner that has been formed on the transfer belt 12. Subsequently, the C (cyan) toner and K (black) toner images are formed in the same manner and transferred by the action of the first transfer rollers 10C and 10B. Thus, YMCK toner images are formed on the transfer belt 12. This is a so-called tandem process.
A color image is formed on the transfer belt 12 by superimposing the four color toner images in registration. After the last transfer of the B toner image, the four color toner images are transferred collectively to the paper 19 fed by a feeding cassette (not shown) at matched timing by the action of the second transfer roller 14. In this case, the follower roller 13 is grounded, and a direct voltage of +1 kV is applied to the second transfer roller 14. The toner images transferred to the paper 19 are fixed by a pair of fixing rollers 201 and 202. Then, the paper 11 is ejected through a pair of ejecting rollers (not shown) to the outside of the apparatus. The toner that is not transferred and remains on the transfer belt 12 is cleaned by the belt cleaner blade 16 to prepare for the next image formation.
Table 17 shows the results of visual images formed by the electrophotographic apparatus in
The charge amount was measured by a blow-off method using frictional charge with a ferrite carrier. Specifically, under the environmental conditions of 25° C. and 45% RH, 0.3 g of sample was taken to evaluate the durability, and a nitrogen gas was blown on the sample at 1.96×104 Pa for 1 minute.
When visual images were formed by using a developer, a high image density was achieved, and there was neither background fog in the non-image portion nor toner scattering. Thus, high-resolution images having a high image density of 1.3 or more were obtained. Moreover, during the long-term durability test with 100,000 sheets of A4 paper, the flowability and the image density were not changed much, and stable characteristics were maintained. The solid images in development also had good uniformity. No developing memory was generated.
Moreover, no streak occurred in the images over continuous use. There was almost no spent of the toner components on the carrier. Both a change in carrier resistance and a decrease in charge amount were suppressed. The charge build-up property was good even after quick supply of the toner. Fog was not increased under high humidity conditions. Moreover, high saturation charge was maintained over a long period of use. The charge amount hardly varied at low temperature and low humidity. Even if the mixing ratio of the toner to the carrier was changed by 5 to 20 wt %, changes in image density and image quality (such as background fog) were small, so that the toner concentration was controlled widely. With respect to the transfer properties, the transfer voids were not a problem for practical use, and the transfer efficiency was about 95%. The filming of the toner on the photoconductive member or the transfer belt also was not a problem for practical use. A cleaning failure of the transfer belt did not occur. There was almost no disturbance or scattering of the toner during fixing. In the case of a full color image formed by superimposing three colors, a transfer failure did not occur, and a paper was not wound around the fixing belt.
For the developers cm21 to cm23, the charge was raised, and considerable fog was generated. Toner filming, which was attributed to suspended particles, occurred on the photoconductive member. When the solid images were developed continuously by two-component development, and then the toner was supplied quickly, the charge was decreased, and fog was increased. This phenomenon became worse, particularly under high humidity conditions.
Table 18 shows the results of the evaluation of the fixability, offset resistance, high-temperature storage stability, and winding of paper around the fixing belt of a full color image.
A solid image was fixed in an amount of 1.2 mg/cm2 at a process speed of 125 mm/s by using a fixing device provided with an oilless belt, and the OHP transmittance (fixing temperature: 160° C.), the minimum fixing temperature, and the temperature at which high-temperature offset occurs were measured. The OHP transmittance was measured with 700 nm light by using a spectrophotometer (U-3200 manufactured by Hitachi, Ltd.). As to the storage stability, the state of the toner was evaluated after being left standing at 55° C. for 24 hours.
For the toners TM1 to TM16, paper jam did not occur in the nip portion of the fixing device. When a full color solid image was fixed on plain paper, no offset occurred until 200,000 sheets. Even if a silicone or fluorine-based fixing belt was used without oil, the surface of the belt did not wear. The OHP transmittance was 80% or more. The offset resistance temperature range was increased by using a fixing roller without oil. Moreover, agglomeration hardly was observed in the storage stability test of 55° C. for 24 hours (indicated by ◯).
For the toner tm21, the offset resistance was slightly low, and a margin of the fixable range was narrow. For the toners tm22 and tm23, the storage stability was degraded due to the effect of suspended wax or resin particles remaining in the toner.
Table 19 shows the glossiness of a solid image portion at a fixing temperature (° C.). The glossiness was measured with a Gloss Checker IG320 (manufactured by Horiba, Ltd.).
The toners TM1 to TM16 showed the characteristics that a change in image glossiness was small in a wide range of fixing temperatures. On the other hand, the image glossiness of the toners tm21 to tm 23 increased with the fixing temperature, and such a change in image glossiness was large, namely, a so-called “shiny” image was generated.
The present invention is useful not only for an electrophotographic system including a photoconductive member, but also for a printing system in which the toner adheres directly on paper or the toner including a conductive material is applied on a substrate as a wiring pattern.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2005-078904 | Mar 2005 | JP | national |
| 2005-078905 | Mar 2005 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2006/302318 | 2/10/2006 | WO | 00 | 9/18/2007 |
