JP2010277112A - Toner for electrostatic latent image development - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a toner for electrostatic latent image development which effectively prevents the generation of filming. <P>SOLUTION: The toner for electrostatic latent image development is obtained by adding an external additive to a toner particle containing a binder resin and a colorant, and satisfies following conditions (B) and (b1). (B) A metal oxide is added as the external additive; and (b1) the isolation rate of the metal oxide is 30 to 60%. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

  The present invention relates to an electrostatic latent image developing toner that is suitably used in an image forming apparatus using an electrophotographic method, and that effectively prevents filming generated on a latent image carrier.

  In the electrophotographic method, an electrostatic latent image formed on a latent image carrier (photoconductor) is developed with a toner containing a colorant, and the resulting toner image is transferred onto a transfer member, which is heated on a roll or the like. In this image forming method, an image is obtained by fixing with the toner image, while the latent image carrier is cleaned to form an electrostatic latent image again.

  In general, not all developed toner is transferred, and some toner remains on the photoreceptor. It is in contact with the photoreceptor like an irregular shaped toner such as a kneading and pulverizing method, or a toner in which some of the toner particles are fused to form a grape shape due to stirring stress in the developing machine. Alternatively, the toner may be contacted at many points and has high adhesion, or the toner may not be transferred even after development due to increased adhesion to the photoreceptor due to small particle size and high charge.

  In recent years, many polymerized toners that can make the particle size of the toner uniform have been introduced. However, due to non-uniformity and non-uniformity of the material during toner preparation, the above-described stress in the developing machine can be avoided. However, there are not a few toners that have become grape-like from the beginning. Further, in order to obtain a high-quality image, the toner has been actively reduced in particle size, but there are actually toners having a distribution in the particle size and a small particle size. Further, a toner aiming at low-temperature fixing has been proposed in order to increase copy productivity, but this toner is generally soft and there is a toner that is fused by stress in the developing machine. As described above, there is toner that remains on the photoreceptor regardless of the production method.

So-called untransferred toner remaining on the photoconductor is removed by a cleaner system such as a blade installed on the photoconductor. At this time, grape-like toner and irregular-shaped toner are easily removed, but the small particle size This toner is prone to poor cleaning and is a problem.
Further, when cleaning is performed using a blade, the transfer residual toner is dammed up at the blade nip portion and cleaned. However, even the grape-like toner and the irregular toner are combined with a toner having a small particle diameter to collect toner in the cleaning blade ( Hereinafter, the total amount of force that the blade receives during cleaning may increase. As a result, the force that the toner in the toner dam portion receives from the cleaning blade becomes strong and adheres to the photosensitive member, causing filming.
In addition, soft toner intended for low-temperature fixing is likely to adhere to the photoreceptor due to the force received from the cleaning blade.

Furthermore, when the toner to which the external additive is added is subjected to stress in the developing machine, the external additive is generally harder than the toner, so that the external additive tends to be embedded in the toner. The toner in which the external additive is embedded has a large contact area with the photoreceptor, and the adhesion is increased, so that the toner tends to remain on the photoreceptor. As a result, the total amount of force that the blade receives during cleaning increases and adheres to the photoreceptor, causing filming.
Even when the cleaning method other than the blade is used, if the surface contaminants are removed by rubbing the surface of the photoreceptor, the same drawbacks exist.

  In order to prevent the filming, a countermeasure for reducing the residual toner can be considered. For example, a method for controlling the residual toner by defining the amount of the external external additive is disclosed (for example, patents). Reference 1 or 2). However, it is not sufficient from the viewpoint of long-term reliability that external additives are buried in the toner, and even if the amount of residual toner is reduced, eventually a clump of toner is generated at the blade portion, and filming occurs. To do.

  There is also a method of adding conductive fine powder as a cleaning aid. However, although it is suitable for cleaning the toner adhering to the photoconductor, there is a risk of scratching the surface of the photoconductor. As a result, the fine powder of toner is trapped in the surface of the photoconductor and cleaned. Cannot be achieved, leading to filming. Moreover, the method of prescribing | regulating the release rate of the said electroconductive fine powder is disclosed (for example, refer patent document 3). However, depending on the toner particles used, there was no filming prevention effect, and it was not yet satisfactory.

JP 2001-22118 A JP 2002-278261 A JP 2004-126575 A

  The present invention has been made in order to eliminate the above-mentioned conventional drawbacks. That is, an object of the present invention is to provide a toner for developing an electrostatic latent image that can effectively prevent the occurrence of filming. There is to do.

The above conventional problems are achieved by the present invention described below. That is, the electrostatic charge developing toner of the present invention is
< 1 > An electrostatic latent image developing toner obtained by adding a metal oxide as an external additive to toner particles containing a binder resin and a colorant, and satisfying the following condition (b1): An electrostatic latent image developing toner.
(B1) The liberation rate of the metal oxide is 30 to 60%.

< 2 > The toner for developing an electrostatic latent image according to < 1 >, wherein the metal oxide contains monodispersed spherical silica having a volume average particle diameter of 80 to 1000 nm.

< 3 > The electrostatic image developing toner according to < 1 > or < 2 >, wherein the binder resin contains an aliphatic crystalline polyester resin.

< 4 > For electrostatic image development according to any one of < 1 > to < 3 >, wherein the ratio of the crystalline polyester resin in the binder resin is 2 to 40% by mass. Toner.

  <5> The toner particles according to any one of <1> to <4>, wherein the toner particles have a weight average molecular weight of a binder resin in a surface portion larger than a weight average molecular weight of an internal binder resin. The toner for developing an electrostatic latent image according to the item.

  According to the present invention, it is possible to provide an electrostatic latent image developing toner that can effectively prevent filming.

The electrostatic latent image developing toner shown as a reference example in the present invention is an electrostatic latent image developing toner obtained by adding conductive fine powder as an external additive to toner particles containing a binder resin and a colorant. The toner satisfies the following conditions (a1) and (a2) (hereinafter, this toner is referred to as “first toner”. The first toner is shown as a reference example in the present invention as described above . is intended).

(A1) The release rate of the conductive fine powder is 50 to 90%.
(A2) The number average particle size distribution index G of the toner particles represented by the following formula is 1.20 or less
Formula: Particle size distribution index G = D50 / D16
(In the formula, D16 represents the number average particle diameter that is accumulated 16% from the small particle diameter side, and D50 represents the number average particle diameter that is accumulated 50% from the small particle diameter side.)

The first toner can more effectively remove the transfer residual toner remaining on the photoreceptor during image formation by releasing the conductive fine powder at a predetermined ratio and defining the particle size distribution of the toner. Can do.
The mechanism is considered as follows. The conductive fine powder, which is the external additive that has been released, is deposited on the cleaning unit installed on the photoconductor, and as a result, the transfer residual toner remaining on the photoconductor is formed on the photoconductor before forming a toner dam. The remaining toner is removed while scraping the surface of the photoreceptor. In the prior art, toner is trapped by minute scratches on the surface of the photosensitive member and pressed against a blade or the like to cause filming. However, in the first toner, the toner particle size distribution is By controlling the toner, the toner is not trapped by minute scratches on the photosensitive member, and as a result, filming can be prevented.

The electrostatic latent image developing toner according to the present invention is an electrostatic latent image developing toner obtained by adding a metal oxide as an external additive to toner particles containing a binder resin and a colorant. The following condition (b1) is satisfied (hereinafter, this toner is referred to as “second toner”. The second toner is related to the present invention as described above ).
(B1) The liberation rate of the metal oxide is 30 to 60%

The second toner can more effectively remove the transfer residual toner remaining on the photoreceptor during image formation by releasing a predetermined amount of the metal oxide that is an external additive.
The mechanism is considered as follows. Since the metal oxide which is a free external external additive is very charged and adheres to the photoconductor during the toner image formation in the development process and is difficult to be transferred, the free metal oxide is a photoconductor. Is deposited on the cleaning unit installed in As a result, the untransferred toner remaining on the photoreceptor adheres to the untransferred toner remaining on the photoreceptor before the toner dam is formed, and filming can be prevented by facilitating cleaning.

  Hereinafter, in describing the present invention in detail, first, the characteristic portions of the first toner and the second toner of the present invention will be described in detail, and then the composition and manufacturing method common to both toners will be described.

<First toner>
-Number average particle size distribution index of toner particles-
The first toner of the present invention has an essential requirement that the number average particle size distribution index G of toner particles represented by the following formula is 1.20 or less.
Formula: Particle size distribution index G = D50 / D16
(In the formula, D16 represents the number average particle diameter that is accumulated 16% from the small particle diameter side, and D50 represents the number average particle diameter that is accumulated 50% from the small particle diameter side.)

  The value of the number average particle size distribution index G is further preferably 1.18 or less, and particularly preferably 1.17 or less. When the number average particle size distribution index G exceeds 1.20, the toner is trapped by minute scratches on the surface of the photoreceptor, and filming occurs on the surface of the photoreceptor. The lower limit is not particularly limited, but a value of 1.13 or more is preferable from the viewpoint that production is generally possible.

-Measuring method of average particle diameter of toner particles-
The number average particle diameter was measured by the following means.
A Coulter Multisizer II type (manufactured by Beckman-Coulter) was used as the measuring apparatus, and an ISOTON-II (manufactured by Beckman-Coulter) was used as the electrolyte.
As a measurement method, 10 mg of a measurement sample is added to 2 ml of a 5% aqueous solution of a surfactant (sodium alkylbenzenesulfonate) as a dispersant. This was added to 100 ml of the electrolytic solution. The electrolytic solution in which the sample is suspended is subjected to a dispersion treatment with an ultrasonic disperser for about 1 minute, and the particle size distribution of particles of 2 to 60 μm is measured using the Coulter counter TA-II with an aperture diameter of 100 μm. The number average distribution was obtained. The number of particles to be measured was 50,000.
Next, for the particle size distribution of the toner, a cumulative number distribution is drawn from the smaller particle size with respect to the divided particle size range (channel), and the cumulative number average particle size of 16% is D16. The number average particle diameter at 50% was defined as D50.

  As a method for controlling the number average particle size distribution index G within the above range, there is a method using both a metal salt of an inorganic acid and a metal salt polymer as an aggregating agent used in the production of toner particles. The reason for this is not clear, but the particles used in the toner have a certain particle size distribution, and particles having a small particle size distribution, specifically, particles in the range of 10 to 150 nm are aggregated with a metal salt of an inorganic acid. The particles in the range of about 150 to 300 nm can be agglomerated by the metal salt polymer and, as a result, can cope with a certain degree of particle size distribution, so that the range of the particle size distribution index G can be achieved. It is done.

Specific examples of the inorganic acid metal salts include acids such as hydrochloric acid, sulfuric acid, nitric acid, acetic acid and oxalic acid, magnesium chloride, sodium chloride, aluminum sulfate, calcium sulfate, ammonium sulfate, aluminum nitrate, silver nitrate and sulfuric acid. Examples thereof include copper and sodium carbonate, and aluminum sulfate is preferably used because it is colorless and transparent and has high cohesive strength.
Specific examples of the metal salt polymer include polyaluminum chloride and polyaluminum hydroxide, and polyaluminum chloride is particularly preferably used.

-Free rate of conductive fine powder-
In addition, the first toner of the present invention has an essential requirement that at least a conductive fine powder is added as an external additive and that the release rate of the conductive fine powder is 50 to 90%. Furthermore, it is preferably 55 to 85%, particularly preferably 60 to 80%.
When the liberation ratio is in the range of 50 to 90%, the transfer residual toner on the photoreceptor can be removed well before the toner dam is formed, and filming can be effectively generated. Can be prevented. When the liberation ratio is less than 50%, the effect of removing the transfer residual toner is small, and the effect of removing the toner dam that causes filming cannot be obtained. On the other hand, when it exceeds 90%, a load is excessively applied to a cleaning device such as a blade, which adversely affects maintainability.

-Measurement method of release rate-
The liberation rate of the conductive fine powder is measured as follows.
First, an elemental analysis of individual particles (toner particles or free conductive fine powder) in the toner is performed with a particle analyzer PT-1000 (manufactured by Yokogawa Electric Corporation), and data of 1000 particles is obtained. Note that helium gas was used for measurement with the particle analyzer PT-1000. When the emission voltage of carbon derived from the binder resin of the toner particles is X and the emission voltage due to the element derived from the external additive is Y, the detected fine powder is a conductive fine powder that is detected when X = 0. is there. From the data thus obtained, the liberation rate was determined from the number of free conductive fine powders in the 1000 particles.

  Examples of a method for controlling the liberation rate of the conductive fine powder within the above range include control by adjusting the surface hardness of the toner particles. In general, the external additive easily aggregates, and the aggregate of the external additive adheres to the toner surface while being destroyed by stirring with the toner particles. At this time, if the hardness of the toner surface is low, the external additive is embedded in the toner. On the other hand, when the hardness is high, the aggregation becomes difficult to break. In order to destroy the aggregated particles of the external additive, it is presumed that the contact surface of the external additive with the toner surface is buried to some extent, so that the aggregation is destroyed. Therefore, by increasing the molecular weight of the toner surface portion compared to the internal molecular weight, the surface hardness is increased and the internal hardness is kept soft to some extent, so that when the toner collides with the external additive aggregated particles, Although the hardness of the toner surface is high, the release rate can be controlled while the influence of the surface hardness is moderately suppressed by the stress generated inside, thereby destroying the aggregation of the external additive.

  Next, specific examples of the conductive fine powder will be given. Examples of the conductive fine powder that can be used in the present invention include metal fine powders such as copper, gold, silver, aluminum, and nickel; zinc oxide, titanium oxide, tin oxide, aluminum oxide, indium oxide, silicon oxide, and oxide. Among metal oxides such as magnesium, barium oxide, molybdenum oxide, iron oxide, tungsten oxide and cerium oxide; metal compounds such as molybdenum sulfide, cadmium sulfide and potassium titanate, or composite oxides thereof, the primary particles are aggregated. Conductive fine powder having an aggregate can be used, and among these, cerium oxide is preferred from the viewpoint of resistance and transmittance. It is also preferable to use conductive fine powder having an adjusted particle size distribution in order to adjust the particle size and particle size distribution as a developer.

  In addition to the conductive fine powder, in order to control the fluidity and chargeability of the toner, it is preferable to add other additives to sufficiently coat the surface of the toner particles. Other additives used include inorganic compounds and organic granules. Examples of the inorganic compound include all particles usually used as external additives on the toner surface, such as alumina, titania, calcium carbonate, magnesium carbonate, tricalcium phosphate, and cerium oxide. For example, all particles used as external additives on the normal toner surface, such as vinyl resin, polyester resin, silicone resin, fluorine resin and the like, can be mentioned. Further, a lubricant can be added. Examples of the lubricant include fatty acid amides such as ethylene bisstearylamide and oleic acid amide, and fatty acid metal salts such as zinc stearate and calcium stearate.

<Second toner>
Next, the second toner of the present invention will be described.
The second toner has an essential requirement that at least a metal oxide is added as an external additive and that the liberation rate of the metal oxide is 30 to 60%. Furthermore, it is preferable that it is 35 to 60%, and it is especially preferable that it is 40 to 60%.
When the liberation ratio is in the range of 30 to 60%, before the transfer residual toner on the photoconductor forms a toner dam, the metal oxide adheres to the transfer residual toner, and the cleaning by the cleaning device is performed well. The occurrence of filming can be effectively prevented. When the liberation rate is less than 30%, the effect of good cleaning properties of the transfer residual toner is small, and the effect of removing the toner dam that causes filming cannot be obtained. On the other hand, when it exceeds 60%, a load is excessively applied to a cleaning device such as a blade, which adversely affects maintainability.

The measurement of the release rate of the metal oxide in the second toner can be performed using the same method as the measurement method of the release rate of the conductive fine powder in the first toner.
Further, as a method for controlling the liberation rate of the metal oxide within the above range, control by adjusting the surface hardness of the toner particles may be mentioned, which is the same as the method for controlling the liberation rate of the conductive fine powder in the first toner. It can be done using the method.

  Next, specific examples of the metal oxide will be given. Examples of the metal oxide that can be used in the present invention include silica, aluminum oxide, zinc oxide, titanium oxide, tin oxide, and iron oxide. Among these, silica is particularly preferable. The reason why silica is preferable is that silica is highly charged, easily adheres to the photoreceptor even in a free state, and has an appropriately high electrical resistance, so that it is difficult to transfer. Therefore, it can be easily supplied to the cleaning unit, and the effect of the present invention can be obtained more remarkably.

  The silica used in the present invention preferably has a volume average particle size of 80 to 1000 nm. If the volume average particle size is less than 80 nm, it tends to not work effectively to reduce non-electrostatic adhesion. In particular, due to stress in the developing machine, the toner particles are easily embedded in the toner particles and may not meet the purpose of releasing the additive of the present invention. On the other hand, if it exceeds 1000 nm, it tends to be detached from the toner particles and is suitable for the purpose of releasing the additive of the present invention, but the transfer residual toner tends not to adhere to the toner remaining on the photoreceptor before the toner dam is formed. This is not preferable. A more preferable range is 80 to 500 nm, and a particularly preferable range is 150 to 300 nm.

  Here, as the particle diameter measurement method when the particle diameter to be measured is less than 2 μm like the external additive such as silica, a laser diffraction particle size distribution measuring device (LA-700: manufactured by Horiba, Ltd.) is used. Used. As a measurement method, a sample in a dispersion is adjusted to have a solid content of about 2 g, and ion exchange water is added thereto to make about 40 ml. This is put into the cell until an appropriate concentration is reached, waits for about 2 minutes, and is measured when the concentration in the cell becomes almost stable. The volume average particle diameter of each obtained channel was accumulated from the smaller one, and the place where the accumulation reached 50% was defined as the volume average particle diameter.

  The silica is preferably monodispersed and spherical. Monodispersed spherical silica can be uniformly dispersed on the surface of the toner particles to obtain a stable spacer effect. Here, the definition of the monodispersion in the present invention can be discussed in terms of the standard deviation with respect to the average particle diameter including aggregates, and the standard deviation is preferably a volume average particle diameter D50 × 0.22 or less. In addition, the definition of the sphere in the present invention can be discussed in terms of Wadell's sphericity, and the sphericity is preferably 0.6 or more, and more preferably 0.8 or more.

  The monodispersed spherical silica having a volume average particle size of 80 to 1000 nm in the present invention can be obtained by a sol-gel method which is a wet method. The true specific gravity can be controlled to be lower than that of the vapor phase oxidation method because it is produced by a wet method and without firing. Further, it is possible to further adjust by controlling the type of hydrophobic treatment agent or the amount of treatment in the hydrophobization treatment step. The particle size can be freely controlled by the hydrolysis of the sol-gel method, the weight ratio of alkoxysilane, ammonia, alcohol, water in the condensation polymerization step, the reaction temperature, the stirring rate, and the supply rate. Monodisperse and spherical shapes can also be achieved by making this technique.

  Specifically, tetramethoxysilane is dropped and stirred while applying temperature using ammonia water as a catalyst in the presence of water and alcohol. Next, the silica sol suspension obtained by the reaction is centrifuged to separate into wet silica gel, alcohol and aqueous ammonia. A solvent is added to wet silica gel to form a silica sol again, and a hydrophobizing agent is added to hydrophobize the silica surface. A general silane compound can be used as the hydrophobizing agent. Next, the target monodispersed spherical silica can be obtained by removing the solvent from the hydrophobized silica sol, drying, and sieve. Further, the silica thus obtained may be treated again. The production method of monodispersed spherical silica in the present invention is not limited to the production method.

A water-soluble silane compound can be used. Examples of such silane compounds include compounds represented by the following chemical structural formula.
R _a SiX _4-a
(In the formula, a is an integer of 0 to 3, R represents an organic group such as a hydrogen atom, an alkyl group and an alkenyl group, and X represents a hydrolyzable group such as a chlorine atom, a methoxy group and an ethoxy group. To express.)

  As the silane compound, any of chlorosilane, alkoxysilane, silazane, and a special silylating agent can be used. Specifically, methyltrichlorosilane, dimethyldichlorosilane, trimethylchlorosilane, phenyltrichlorosilane, diphenyldichlorosilane, tetramethoxysilane, methyltrimethoxysilane, dimethyldimethoxysilane, phenyltrimethoxysilane, diphenyldimethoxysilane, tetraethoxysilane, Methyltriethoxysilane, dimethyldiethoxysilane, phenyltriethoxysilane, diphenyldiethoxysilane, isobutyltrimethoxysilane, decyltrimethoxysilane, hexamethyldisilazane, N, O- (bistrimethylsilyl) acetamide, N, N-bis (Trimethylsilyl) urea, tert-butyldimethylchlorosilane, vinyltrichlorosilane, vinyltrimethoxysilane, vinyltriethoxy Silane, γ-methacryloxypropyltrimethoxysilane, β- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropylmethyldiethoxysilane, γ-mercapto Representative examples include propyltrimethoxysilane and γ-chloropropyltrimethoxysilane. Particularly preferably, the hydrophobizing agent in the present invention includes dimethyldimethoxysilane, hexamethyldisilazane, methyltrimethoxysilane, isobutyltrimethoxysilane, decyltrimethoxysilane and the like.

  In addition, in order to control the fluidity and chargeability of the toner, it is preferable to sufficiently coat the surface of the toner particles. Since the above-mentioned silica alone may not provide a sufficient coating, an inorganic material having a small particle diameter is used. It is preferable to use a compound or organic particles in combination. As the inorganic compound having a small particle size, an inorganic compound having a volume average particle size of 80 nm or less is preferable, and an inorganic compound having a particle size of 50 nm or less is more preferable. Specifically, for example, all the particles used as external additives on the normal toner surface such as alumina, titania, calcium carbonate, magnesium carbonate, tricalcium phosphate, cerium oxide, etc. For example, all particles used as external additives on the normal toner surface, such as vinyl resin, polyester resin, silicone resin, fluorine resin and the like, can be mentioned. Further, a lubricant can be added. Examples of the lubricant include fatty acid amides such as ethylene bisstearylamide and oleic acid amide, and fatty acid metal salts such as zinc stearate and calcium stearate.

<Composition of toner particles>
Next, the electrostatic charge developing toner composition of the present invention containing the first toner and the second toner will be described. The toner particles in the present invention comprise at least a binder resin and a colorant.

-Binder resin-
Binder resins used include styrenes such as styrene and chlorostyrene; monoolefins such as ethylene, propylene, butylene, and isoprene; vinyl esters such as vinyl acetate, vinyl propionate, vinyl benzoate, and vinyl butyrate; Α-methylene aliphatic monocarboxylic acid esters such as methyl acrylate, ethyl acrylate, butyl acrylate, dodecyl acrylate, octyl acrylate, phenyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, dodecyl methacrylate Homopolymers and copolymers such as vinyl ethers such as vinyl methyl ether, vinyl ethyl ether, vinyl butyl ether; vinyl ketones such as vinyl methyl ketone, vinyl hexyl ketone, vinyl isopropenyl ketone; Can.

  Particularly representative binder resins include polystyrene, styrene-alkyl acrylate copolymer, styrene-alkyl methacrylate copolymer, styrene-acrylonitrile copolymer, styrene-butadiene copolymer, styrene-maleic anhydride copolymer. Examples thereof include a polymer, polyethylene, and polypropylene. Further examples include polyester, polyurethane, epoxy resin, silicone resin, polyamide, modified rosin, paraffin wax and the like.

  The binder resin is preferably excellent in sharp melt property at the time of fixing, and from the viewpoint of obtaining low-temperature fixability and high glossiness in a fixed image, it is preferable to use an amorphous resin and a crystalline resin in combination.

  The amorphous resin has only a stepwise endothermic change, not a clear endothermic peak, in a thermal analysis measurement using differential scanning calorimetry (DSC). It refers to those that are thermoplasticized at temperatures above that. The crystalline resin refers to a resin having a clear endothermic peak, not a stepwise change in endothermic amount in differential scanning calorimetry (DSC).

  As the amorphous resin, each of the exemplified resins can be used, but it is preferable to use an amorphous polyester resin from the viewpoint of chargeability.

  The crystalline resin is not particularly limited as long as it is a resin having crystallinity, and specifically includes a crystalline polyester resin, a crystalline vinyl resin, and the like. A crystalline polyester resin is preferred from the viewpoint of chargeability and adjustment of the melting point within a preferred range. An aliphatic crystalline polyester resin having an appropriate melting point is more preferable.

  The crystalline polyester resin is synthesized from an acid (dicarboxylic acid) component and an alcohol (diol) component. In the present invention, the “acid-derived component” refers to an acid component before synthesis of the polyester resin. The “alcohol-derived constituent component” refers to a constituent portion that was an alcohol component before the synthesis of the polyester resin. In the present invention, in the case of a polymer obtained by copolymerizing other components with respect to the crystalline polyester main chain, when the other components are 50% by mass or less, this copolymer is also called crystalline polyester.

  The acid-derived constituent component is preferably an aliphatic dicarboxylic acid, and particularly preferably a linear carboxylic acid. Examples of the linear carboxylic acid include oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelic acid, sebacic acid, 1,9-nonanedicarboxylic acid, 1,10- Decanedicarboxylic acid, 1,11-undecanedicarboxylic acid, 1,12-dodecanedicarboxylic acid, 1,13-tridecanedicarboxylic acid, 1,14-tetradecanedicarboxylic acid, 1,16-hexadecanedicarboxylic acid, 1,18-octadecane Dicarboxylic acid, etc., or lower alkyl esters and acid anhydrides thereof. Among these, those having 6 to 10 carbon atoms are preferable from the viewpoint of crystal melting point and chargeability. In order to increase the crystallinity, these linear dicarboxylic acids are preferably used in an amount of 95 mol% or more, more preferably 98 mol% or more of the acid component.

  The other monomer is not particularly limited. For example, a conventionally known divalent or carboxylic acid which is a monomer component as described in Polymer Data Handbook: Basics (Science of Polymer Science: Bafukan). And divalent alcohol. Specific examples of these monomer components include divalent carboxylic acids such as phthalic acid, isophthalic acid, terephthalic acid, naphthalene-2,6-dicarboxylic acid, naphthalene-2,7-dicarboxylic acid, and cyclohexanedicarboxylic acid. And dibasic acids such as these, anhydrides thereof, and lower alkyl esters thereof. These may be used individually by 1 type and may use 2 or more types together.

  As the acid-derived constituent component, in addition to the above-mentioned aliphatic dicarboxylic acid-derived constituent component, a constituent component such as a dicarboxylic acid-derived constituent component having a sulfonic acid group is preferably included.

  The dicarboxylic acid having a sulfonic acid group is effective in that it can favorably disperse a coloring material such as a pigment. Further, when a resin fine particle dispersion is prepared by emulsifying or suspending the entire resin in water, if a sulfonic acid group is present, it can be emulsified or suspended without using a surfactant as described later. Examples of such a dicarboxylic acid having a sulfone group include, but are not limited to, 2-sulfoterephthalic acid sodium salt, 5-sulfoisophthalic acid sodium salt, and sulfosuccinic acid sodium salt. Moreover, these lower alkyl esters, acid anhydrides, etc. are also mentioned. Among these, 5-sulfoisophthalic acid sodium salt is preferable in terms of cost. The content of the dicarboxylic acid having a sulfonic acid group is preferably 0.1 to 2.0 constituent mol%, and preferably 0.2 to 1.0 constituent mol%. When the content is more than 2 constituent mol%, the chargeability may be deteriorated. In the present invention, “constituent mol%” refers to a percentage when each constituent component (acid-derived constituent component, alcohol-derived constituent component) in the polyester resin is 1 unit (mol).

  The alcohol component is preferably an aliphatic dialcohol, such as ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,7-heptanediol. 1,8-octanediol, 1,9-nonanediol, 1,10-decanediol, 1,11-dodecanediol, 1,12-undecanediol, 1,13-tridecanediol, 1,14-tetradecanediol 1,18-octadecanediol, 1,20-eicosanediol, etc., among which those having 6 to 10 carbon atoms are preferred from the viewpoint of crystal melting point and chargeability. In order to enhance crystallinity, these linear dialcohols are preferably used in an amount of 95 mol% or more, more preferably 98 mol% or more of the alcohol constituent.

  Other divalent dialcohols include, for example, bisphenol A, hydrogenated bisphenol A, ethylene oxide or (and) propylene oxide adducts of bisphenol A, 1,4-cyclohexanediol, 1,4-cyclohexanedimethanol, diethylene glycol, Examples include propylene glycol, dipropylene glycol, 1,3-butanediol, and neopentyl glycol. These may be used individually by 1 type and may use 2 or more types together.

  If necessary, monovalent acids such as acetic acid and benzoic acid, monovalent alcohols such as cyclohexanol and benzyl alcohol, benzenetricarboxylic acid, and naphthalenetricarboxylic acid for the purpose of adjusting the acid value and hydroxyl value. And trihydric alcohols such as anhydrides thereof, lower alkyl esters thereof, glycerin, trimethylolethane, trimethylolpropane, and pentaerythritol can also be used.

  The polyester resin can be used in any combination of the monomer components described above, for example, polycondensation (chemical doujin), polymer experiment (polycondensation and polyaddition: Kyoritsu Publishing) and polyester resin handbook (edited by Nikkan Kogyo Shimbun). And the like, and a transesterification method, a direct polycondensation method, and the like can be used alone or in combination. The molar ratio (acid component / alcohol component) for reacting the acid component with the alcohol component varies depending on the reaction conditions and the like, so it cannot be generally stated, but in the case of direct polycondensation, usually about 1/1. In the case of the transesterification method, ethylene glycol, neopentyl glycol, cyclohexanedimethanol, etc. are often used in excess of monomers that can be distilled off under vacuum. The production of the polyester resin is usually performed at a polymerization temperature of 180 to 250 ° C., and the reaction system is subjected to a reaction while reducing the pressure in the reaction system as necessary to remove water and alcohol generated during the condensation. When the monomer is not dissolved or compatible at the reaction temperature, a solvent having a high boiling point may be added as a solubilizer and dissolved. In the polycondensation reaction, the dissolution auxiliary solvent is distilled off. If there is a monomer with poor compatibility in the copolymerization reaction, the monomer with poor compatibility and the monomer and the acid or alcohol to be polycondensed may be condensed in advance before polycondensation with the main component. .

  Catalysts that can be used in the production of the polyester resin include alkali metal compounds such as sodium and lithium, alkaline earth metal compounds such as magnesium and calcium, and metal compounds such as zinc, manganese, antimony, titanium, tin, zirconium, and germanium. , Phosphorous acid compounds, phosphoric acid compounds, amine compounds, etc., specifically, sodium acetate, sodium carbonate, lithium acetate, lithium carbonate, calcium acetate, calcium stearate, magnesium acetate, zinc acetate, stearic acid Zinc, zinc naphthenate, zinc chloride, manganese acetate, manganese naphthenate, titanium tetraethoxide, titanium tetrapropoxide, titanium tetraisopropoxide, titanium tetrabutoxide, antimony trioxide, triphenylantimony, trib Ruantimony, tin formate, tin oxalate, tetraphenyltin, dibutyltin dichloride, dibutyltin oxide, diphenyltin oxide, zirconium tetrabutoxide, zirconium naphthenate, zirconyl carbonate, zirconyl acetate, zirconyl stearate, zirconyl octylate, germanium oxide, triphenyl Examples of the compound include phosphite, tris (2,4-di-t-butylphenyl) phosphite, ethyltriphenylphosphonium bromide, triethylamine, and triphenylamine. Among these, a tin-based catalyst and a titanium-based catalyst are preferable from the viewpoint of chargeability, and among them, dibutyltin oxide is preferably used.

  The melting point of the crystalline polyester resin is preferably 50 to 120 ° C, more preferably 60 to 110 ° C. If the melting point is lower than 50 ° C., the storage stability of the toner and the storage stability of the toner image after fixing may become a problem. If the temperature is higher than 120 ° C., sufficient low-temperature fixing may not be obtained as compared with conventional toners. In the present invention, the melting point of the crystalline polyester resin is measured using a differential scanning calorimeter (DSC) to be described later. When a plurality of melting peaks are shown, the maximum peak is regarded as the melting point.

  The crystalline polyester resin preferably has a weight average molecular weight in the range of 5000 to 50000, more preferably in the range of 10000 to 30000, as measured by GPC. If the molecular weight is too small, there is a concern that the effect of plasticizing the toner becomes strong and the offset deteriorates. When the molecular weight is too large, the melt viscosity of the toner becomes high and the low-temperature fixability may be deteriorated.

  The acid value of the crystalline polyester resin is preferably 3.0 to 25.0 mgKOH / g. More preferably, it exists in the range of 6.0-20.0 mgKOH / g, More preferably, it exists in the range of 9.0-18.0 mgKOH / g. When the acid value is lower than 3.0 mgKOH / g, the stability as the resin fine particles at the time of aggregation is poor, and when it exceeds 25.0 mgKOH / g, the hygroscopicity of the toner increases and the toner is easily affected by the environment. It is not preferable.

  The amorphous polyester resin can be obtained by using the same monomer as the crystalline polyester resin and using the same method. From the viewpoint of chargeability and fixability, bisphenol A dialcohol and The phthalic acid-based dicarboxylic acid is preferred. Specifically, bisphenol A ethylene oxide disallowed, bisphenol A propylene oxide disallowed, terephthalic acid, and isophthalic acid are mainly used. The amorphous polyester resin may have a crosslinked structure in the molecule. Monomers that form a crosslinked structure include trivalent or higher carboxylic acids such as benzenetricarboxylic acid naphthalenetricarboxylic acid, unsaturated dicarboxylic acids such as maleic acid, fumaric acid, itaconic acid, citraconic acid, and anhydrides thereof. Acid monomers such as lower alkyl esters, and trivalent or higher alcohol monomers such as glycerin, trimethylolethane, trimethylolpropane, and pentaerythritol. These may be used individually by 1 type and may use 2 or more types together.

  The amorphous polyester resin preferably has a weight average molecular weight in the range of 5000 to 30000, more preferably in the range of 7000 to 20000, as measured by GPC. If the molecular weight is too small, the offset property may deteriorate. If the molecular weight is too large, the melt viscosity of the toner increases and the low-temperature fixability may deteriorate.

  The acid value of the amorphous polyester resin is preferably 2.0 to 25.0 mgKOH / g. More preferably, it exists in the range of 3.0-20.0 mgKOH / g, More preferably, it exists in the range of 4.0-15.0 mgKOH / g. If the acid value is lower than 2.0 mgKOH / g, the stability as a resin fine particle at the time of aggregation is poor, and if it exceeds 25.0 mgKOH / g, the hygroscopicity of the toner increases and it is easily affected by the environment as a toner. It is not preferable.

  The glass transition temperature of the amorphous polyester resin is preferably in the range of 45 ° C to 80 ° C. More preferably, it exists in the range of 50 to 75 degreeC, More preferably, it exists in the range of 55 to 65 degreeC. If the glass transition temperature is too high, the low-temperature fixability may be impaired. If the glass transition temperature is too low, the storage stability of the toner may deteriorate.

In the toner particles of the present invention, the ratio of the crystalline polyester resin in the total binder resin component is preferably 2 to 40% by mass, and more preferably 2 to 20% by mass. When the content of the crystalline polyester resin is less than 2% by mass, the effect of improving the low-temperature fixability may not be obtained. When the content is more than 40% by mass, the hardness of the toner is lowered and the external additive is embedded. It may become easy to be shortened and the life may be shortened. A part of the crystalline polyester resin is in an amorphous state, and therefore the cause is that the resin strength at room temperature is lower than that of the amorphous resin.
Further, the content of the binder resin in the toner particles is preferably 70 to 98% by mass.

-Colorant-
There is no restriction | limiting in particular as a coloring agent used for this invention, A well-known coloring agent is mentioned, According to the objective, it can select suitably. One colorant may be used alone, or two or more colorants of the same system may be mixed and used. Further, two or more kinds of different colorants may be mixed and used. Further, these colorants may be used after surface treatment.

Specific examples of the colorant used include black, yellow, red, blue, purple, green and white colorants as shown below.
Examples of black pigments include organic and inorganic colorants such as carbon black, aniline black, activated carbon, nonmagnetic ferrite, and magnetite.
Examples of blue pigments include organic and inorganic colorants such as bitumen, cobalt blue, alkali blue lake, Victoria blue lake, fast sky blue, indanthrene blue BC, ultramarine blue, phthalocyanine blue, and phthalocyanine green. It is done.

Yellow pigments include yellow lead, zinc yellow, yellow iron oxide, cadmium yellow, chrome yellow, fast yellow, fast yellow 5G, fast yellow 5GX, fast yellow 10G, benzidine yellow G, benzidine yellow GR, selenium yellow, quinoline yellow, Examples of orange pigments such as permanent yellow NCG include: red yellow lead, molybdenum orange, permanent orange GTR, pyrazolone orange, vulcan orange, benzidine orange G, indanthrene brilliant orange RK, indanthrene brilliant orange GK and the like.
Red pigments include Bengala, cadmium red, red lead, mercury sulfide, watch young red, permanent red 4R, risor red, brilliantamine 3B, brilliantamine 6B, dapon oil red, pyrazolone red, rhodamine B rake, lake red C , Rose Bengal, Eoxin Red, Alizarin Lake, etc., purple pigments, manganese purple, fast violet B, methyl violet lake, etc., organic and inorganic colorants, green pigments: chromium oxide, chrome green, pigment green Examples thereof include organic and inorganic colorants such as B, malachite green lake, and fanal yellow green G.

Examples of white pigments include zinc white, titanium oxide, antimony white, and zinc sulfide. Examples of extender pigments include barite powder, barium carbonate, clay, silica, white carbon, talc, and alumina white.
The content of the colorant in the toner particles is preferably 1 to 15% by mass.

-Release agent-
A release agent can be further added to the toner particles in the present invention. Examples of the release agent used include low molecular weight polyolefins such as polyethylene, polypropylene, and polybutene, silicones that exhibit a softening point when heated, oleic acid amide, erucic acid amide, ricinoleic acid amide, stearic acid amide, and the like. Fatty acid amides, plant waxes such as carnauba wax, rice wax, candelilla wax, tree wax, jojoba oil, animal waxes such as beeswax, montan wax, ozokerite, ceresin, paraffin wax, microcrystalline wax And mineral-based and petroleum-based waxes such as microcrystalline wax and Fischer-Tropsch wax, and modified products thereof.

  In the present invention, it is preferable to use minerals such as paraffin wax, microcrystalline wax, Fischer-Tropsch wax, petroleum wax, and polyalkylene which is a modified product thereof, as the mold release agent. The viscosity η140 at 140 ° C. measured by an E-type viscometer is preferably in the range of 1.5 to 5.0 mPa · s, more preferably in the range of 2.0 to 4.5 mPa · s.

  When the viscosity η140 at 140 ° C. is less than 1.5 mPa · s, the powder fluidity of the toner deteriorates, or the release agent layer formed on the image after fixing becomes non-uniform, resulting in uneven peeling. In some cases, it may cause problems such as uneven image gloss. Also, when the viscosity η is higher than 5.0 mPa · s, the melt viscosity increases and the release property of the release agent decreases, so that between oil and an image fixing member such as a fixing roll during oilless fixing. In addition, there may be a case where the original merit of the mold release agent having a low melt viscosity is lost such that a mold release agent necessary for mold release cannot be supplied and a peeling failure occurs.

  The viscosity η140 of the release agent at 140 ° C. is measured with an E-type viscometer. In the measurement, an E-type viscometer (manufactured by Tokyo Keiki Co., Ltd.) equipped with an oil circulation type thermostatic bath was used. Here, a cone plate having a cone angle of 1.34 ° was used.

  Specifically, the measurement is performed as follows. First, the temperature of the circulation device is set to 140 ° C., and an empty sample measurement cup, an empty reference cup, and a cone are set in the measurement device, and kept at a constant temperature while circulating oil. Next, when the temperature is stabilized, 1 g of the sample is put in the sample measuring cup, and the cone is allowed to stand still for 10 minutes. After stabilization, rotate the cone and measure. The rotational speed of the cone is 60 rpm. The measurement was performed three times, and the average value was defined as a viscosity η140 at 140 ° C.

  Moreover, it is preferable that the main body maximum peak in the differential scanning calorimetry measured according to ASTM D3418-8 is in the range of 85 to 95 ° C, and in the range of 86 to 93 ° C. Is more preferable.

  If the main maximum peak is less than 85 ° C., there may be a problem that an offset is likely to occur. When the temperature exceeds 95 ° C., the toner fixing temperature becomes high, and the smoothness of the surface of the fixed image cannot be obtained. In some cases, a problem such as a decrease in image quality may occur.

For the measurement of the main maximum peak, for example, DSC-7 manufactured by Perkin Elmer is used. The temperature correction of the detection part of the apparatus uses the melting points of indium and zinc, and the correction of heat quantity uses the heat of fusion of indium. As the sample, an aluminum pan was used, an empty pan was set as a control, and the measurement was performed at a heating rate of 10 ° C./min.
The glass transition point and melting point of the binder resin described above were also measured by the same method as described above.

Further, the content in the toner particles determined from the height of the endothermic peak at the maximum endothermic value in the differential thermal analysis of the release agent is preferably in the range of 5 to 10% by mass. More preferably, it is the range of 6.5-8.5 mass%.
If the amount of the release agent is less than 5% by mass, although it is advantageous for the drying treatment of the wet toner described later, a sufficient elution amount for peeling at the time of oilless fixing cannot be obtained, the peelability is impaired, and the surface is roughened. As a result, image glossiness may be reduced. On the other hand, if it exceeds 10% by mass, the transfer of the release agent to the surface of the wet toner is facilitated during drying, and not only the powder fluidity of the toner after drying is lowered, but also a discharge roll for discharging a fixed image. Such a contact mark may occur, and the image quality may be impaired.

<Method for producing toner particles>
Next, a preferred method for producing toner particles in the present invention will be described.
The toner particles include a coagulation step of forming aggregated particles in a dispersion in which at least resin fine particles and colorant particles are dispersed, and a fusion process of heating the aggregated particles and fusing the aggregated particles It is preferable from the viewpoint of obtaining a color toner capable of forming a small particle diameter toner having a sharp particle size distribution and capable of forming a high-quality full-color image.

  In the aggregation step, at least the resin fine particle dispersion containing the binder resin and the colorant dispersion containing the colorant are used, and if necessary, other components such as a release agent dispersion are added and mixed. The prepared dispersion is mixed, an aggregating agent is added thereto, and the mixture is heated while stirring to agglomerate the resin fine particles and the colorant to form aggregated particles.

  The volume average particle diameter of the aggregate particles is preferably in the range of 2 to 9 μm. It is also possible to add resin fine particles (additional fine particles) to the aggregate particles formed in this way to form a coating layer on the surface of the aggregate particles (attachment step). The resin fine particles (additional fine particles) additionally added in this adhesion step need not be the same as the resin fine particle dispersion used in the above-described aggregation step.

  Moreover, it is preferable to mix resin with comparatively high molecular weight, in order to make the resin used for the above-mentioned aggregation process or adhesion process easy to release an external additive. Specifically, a resin having a Z average molecular weight Mz of 100,000 to 500,000 is preferable.

  Next, in the fusing step, for example, heat treatment is performed at a temperature equal to or higher than the glass transition point of the resin, generally 70 to 120 ° C., and the aggregate particles are fused to obtain a toner particle-containing liquid (toner particle dispersion). Next, the obtained toner particle-containing liquid is treated by centrifugal separation or suction filtration to separate the toner particles, and washed 1 to 3 times with ion exchange water. At that time, the cleaning effect can be further enhanced by adjusting the pH. Thereafter, the toner particles are separated by filtration, washed 1 to 3 times with ion exchange water, and dried to obtain toner particles for use in the toner of the present invention.

In the first toner of the present invention, at least conductive fine powder is added as an external additive to the toner particles thus obtained. In this case, the amount of the conductive fine powder added to the toner particles is preferably 0.5 to 10% by mass, more preferably 1 to 7% by mass.
In the second toner, at least a metal oxide is added as an external additive to the toner particles. In this case, the amount of metal oxide added to the toner particles is preferably 0.3 to 15% by mass, more preferably 1 to 10% by mass.

Hereinafter, the present invention will be described in more detail with reference to examples and comparative examples. However, the present invention is not limited to the following examples and comparative examples. In the following, “parts” and “%” represent “parts by mass” and “mass%” unless otherwise specified.
In addition, Examples 1-3 and Comparative Examples 1-3 shown below are all shown as reference examples of the present invention.

First, in preparing the toners used in Examples 1 to 3 and Comparative Examples 1 and 2, the following samples were prepared.
[Preparation of crystalline resin fine particle dispersion]
A heat-dried three-necked flask was charged with 98 parts of dimethyl sebacate, 2 parts of sodium dimethyl-5-sulfonate, 100 parts of 1,6-hexanediol, and 0.3 part of dibutyltin oxide as a catalyst. Then, the air in the container was brought into an inert atmosphere with nitrogen gas, and stirred and refluxed at 180 ° C. for 5 hours with mechanical stirring.

  Thereafter, the temperature was gradually raised to 230 ° C. under reduced pressure, and the mixture was stirred for 4 hours. When it became viscous, it was air-cooled, the reaction was stopped, and crystalline resin 1 was synthesized. The weight average molecular weight (Mw) of the obtained crystalline resin 1 was 30000 by molecular weight measurement (polystyrene conversion) by gel permeation chromatography.

In the present invention, the specific molecular weight of the particles is measured under the following conditions. "
GPC uses “HLC-8120GPC, SC-8020 (manufactured by Tosoh Corporation)”, and the column uses two “TSKgel, SuperHM-H (6.0 mm ID × 15 cm, manufactured by Tosoh Corporation)” THF (tetrahydrofuran) was used as an eluent. As experimental conditions, the sample concentration was 0.5%, and the flow rate was 0.6 ml / min. The experiment was conducted using a sample injection amount of 10 μl, a measurement temperature of 40 ° C., and an IR detector. The calibration curve is “polystylen standard sample TSK standard” manufactured by Tosoh Corporation: “A-500”, “F-1”, “F-10”, “F-80”, “F-380”, “A-2500”. ”,“ F-4 ”,“ F-40 ”,“ F-128 ”, and“ F-700 ”.

  Further, when the melting point (Tm) of the crystalline resin 1 was measured by a differential scanning calorimeter (DSC) by the above-described measuring method, it showed a clear endothermic peak, and the endothermic peak temperature was 66 ° C.

Next, a crystalline resin fine particle dispersion was prepared using the crystalline resin.
-Crystalline resin 1: 90 parts-Ionic surfactant Neogen RK (Daiichi Kogyo Seiyaku): 1.8 parts-Ion exchange water: 210 parts

  The above is heated to 100 ° C., sufficiently dispersed with IKA Ultra Tarrax T50, then dispersed with a pressure discharge type gorin homogenizer for 1 hour, and crystalline resin fine particles having a volume average particle size of 130 nm and a solid content of 30% Dispersion 1 was obtained. The volume average particle size was measured using a laser diffraction particle size distribution measuring device (Horiba, Ltd .: LA-700).

[Preparation of Amorphous Resin Fine Particle Dispersion 1]
-Styrene (Wako Pure Chemical Industries): 325 parts-n-butyl acrylate (Wako Pure Chemical Industries): 100 parts-Acrylic acid (Rhodia Nikka Co., Ltd.): 13 parts-1,10-decanediol diacrylate (new) Nakamura Chemical Co., Ltd.): 1.5 parts ・ Dodecanethiol (Wako Pure Chemical Industries, Ltd.): 3.0 parts

The above components are mixed in advance and dissolved to prepare a solution. A surfactant solution prepared by dissolving 9 parts of an anionic surfactant (Dowfax A211 manufactured by Dow Chemical Co., Ltd.) in 580 parts of ion-exchanged water is added to a flask. Then, 400 parts of the above solution was added, dispersed and emulsified, and slowly stirred and mixed for 10 minutes, and then 50 parts of ion-exchanged water in which 6 parts of ammonium persulfate had been dissolved was added.
Next, after the inside of the flask is sufficiently replaced with nitrogen, the flask is heated with an oil bath while stirring the flask until it reaches 75 ° C., and emulsion polymerization is continued as it is for 5 hours. Obtained.

  When the resin fine particles were separated from the amorphous resin fine particle dispersion 1 and examined for physical properties, the volume average particle size was 195 nm, the solid content in the dispersion was 42%, the glass transition point was 51.5 ° C., and the weight average molecular weight. Mw was 32000.

[Preparation of Amorphous Resin Fine Particle Dispersion 2]
・ Styrene (made by Wako Pure Chemical Industries): 320 parts ・ n-butyl acrylate (made by Wako Pure Chemical Industries): 115 parts ・ Acrylic acid (made by Rhodia Nikka): 13 parts

  A solution prepared by dissolving 1.5 parts of the anionic surfactant Dowfax (manufactured by Dow Chemical Co., Ltd.) in 550 parts of ion-exchanged water is added to the solution obtained by mixing and dissolving the above components, and the mixture is dispersed and emulsified in a flask. While stirring and mixing, 50 parts of ion-exchanged water in which 5.5 parts of ammonium persulfate was dissolved was added. Then, after sufficiently replacing the nitrogen in the flask, the solution in the flask was stirred in an oil bath while stirring. The mixture was heated to 65 ° C., and emulsion polymerization was continued for 5 hours to obtain an anionic amorphous resin fine particle dispersion 2. The volume average particle diameter of the resin fine particles in the amorphous resin fine particle dispersion 2 was 170 nm, the solid content was 42.6%, and the weight average molecular weight (Mw) was 217200.

[Preparation of colorant particle dispersion]
Copper phthalocyanine B15: 3 (manufactured by Dainichi Seika): 45 parts Cationic surfactant Neogen RK (Daiichi Kogyo Seiyaku): 5 parts Ion-exchanged water: 200 parts

  The above components are mixed and pre-dispersed for 10 minutes with a homogenizer (Ultra Turrax: made by IKA), and then dispersed for 15 minutes at a pressure of 245 mPa using an optimizer (anti-collision type wet pulverizer: made by Sugino Machine). A colorant particle dispersion having a volume average particle diameter of 385 nm was obtained.

[Preparation of release agent particle dispersion]
Pentaerythritol behenate wax (melting point 84.5 ° C.): 45 parts Cationic surfactant Neogen RK (Daiichi Kogyo Seiyaku): 5 parts Ion-exchanged water: 200 parts

  The above was heated to 95 ° C., sufficiently dispersed with IKA Ultra Tarrax T50, and then dispersed with a pressure discharge type gorin homogenizer, and the mold was released with a volume average particle size of 220 nm and a solid content in 100 parts of 20%. An agent particle dispersion was obtained.

[Preparation of Toner Particle 1-1]
Amorphous resin fine particle dispersion 1: 280 parts Colorant particle dispersion: 55 parts Release agent particle dispersion: 95 parts

A solution was obtained in which the above components were sufficiently mixed and dispersed with Ultra Turrax T50 in a round stainless steel flask.
Next, with stirring, 0.2 part of polyaluminum chloride and 0.1 part of aluminum sulfate were added to this solution to produce core aggregated particles, and the dispersion operation was continued using an ultra turrax. Further, the solution in the flask was heated to 47 ° C. with stirring in an oil bath for heating and held at 47 ° C. for 60 minutes, and then 100 parts of the amorphous resin fine particle dispersion 1 was gently added to the amorphous resin fine particles. 50 parts of dispersion 2 was added to produce core / shell aggregated particles.

Thereafter, a 0.5 mol / L sodium hydroxide aqueous solution was added to adjust the pH of the solution to 6.5, and then the stainless steel flask was sealed and heated to 98 ° C. while continuing to stir using a magnetic seal. A 3 mol / L nitric acid aqueous solution was added to adjust the pH of the solution to 4.2, and then a 0.3 mol / L citric acid aqueous solution was added to adjust the pH of the solution to 3.1, and the solution was held for 5 hours. After cooling, a blue toner was obtained.
Next, the blue toner dispersed in the solution was filtered, thoroughly washed with ion exchange water, and then subjected to solid-liquid separation by Nutsche suction filtration. This was further redispersed in 3 L of ion exchanged water at 40 ° C., and stirred and washed at 300 rpm for 15 minutes.
This was repeated five more times, and when the filtrate had a pH of 7.01 and an electrical conductivity of 15.8 μS / cm, solid-liquid separation was performed using No5A filter paper by Nutsche suction filtration. The solid matter thus obtained was vacuum-dried for 12 hours to obtain toner particles 1-1. The number average particle size distribution index G was 1.18.

[Preparation of Toner Particles 1-2]
-Crystalline resin fine particle dispersion: 115 parts-Amorphous resin fine particle dispersion 1: 190 parts-Colorant particle dispersion: 55 parts-Release agent particle dispersion: 95 parts

  As an adhesion process, the toner particles 1-2 were prepared in the same procedure as the toner particles 1-1 except that 125 parts of the amorphous resin fine particle dispersion 1 and 25 parts of the amorphous resin fine particle dispersion 2 were added. Produced. The number average particle size distribution index G was 1.16.

[Preparation of Toner Particles 1-3]
-Crystalline resin fine particle dispersion: 115 parts-Amorphous resin fine particle dispersion 1: 190 parts-Colorant particle dispersion: 55 parts-Release agent particle dispersion: 95 parts

  As an adhesion process, except that 75 parts of the amorphous resin fine particle dispersion 1 and 75 parts of the amorphous resin fine particle dispersion 2 are added, the toner particles 1-3 are prepared in the same procedure as the toner particles 1-1. Produced. The number average particle size distribution index G was 1.19.

[Preparation of Toner Particles 1-4]
-Crystalline resin fine particle dispersion: 115 parts-Amorphous resin fine particle dispersion 1: 190 parts-Colorant particle dispersion: 55 parts-Release agent particle dispersion: 95 parts

  As an adhesion process, except that 140 parts of the amorphous resin fine particle dispersion 1 and 10 parts of the amorphous resin fine particle dispersion 2 are added, toner particles 1-4 are prepared in the same manner as the toner particles 1-1. Produced. The number average particle size distribution index G was 1.14.

[Preparation of Toner Particles 1-5]
-Crystalline resin fine particle dispersion: 115 parts-Amorphous resin fine particle dispersion 1: 190 parts-Colorant particle dispersion: 55 parts-Release agent particle dispersion: 95 parts

  As an adhesion step, toner particles 1-5 were added in the same procedure as toner particles 1-1 except that 25 parts of amorphous resin fine particle dispersion 1 and 125 parts of amorphous resin fine particle dispersion 2 were added. Produced. The number average particle size distribution index G was 1.20.

[Preparation of Toner Particles 1-6]
-Crystalline resin fine particle dispersion: 125 parts-Amorphous resin fine particle dispersion 1: 180 parts-Colorant particle dispersion: 55 parts-Release agent particle dispersion: 95 parts

  As an adhesion process, toner particles 1-6 were prepared in the same procedure as toner particles 1-1 except that 20 parts of amorphous resin fine particle dispersion 1 and 130 parts of amorphous resin fine particle dispersion 2 were added. Produced. The number average particle size distribution index G was 1.22.

[Production of carrier]
Ferrite particles (volume average particle size: 50 μm): 100 parts Toluene: 14 parts Styrene-methacrylate copolymer (component ratio: 90/10, weight average molecular weight 80000): 2 parts Carbon black (R330: Cabot Corporation) Made): 0.2 parts

  First, the above components except for ferrite particles are stirred with a stirrer for 10 minutes to prepare a dispersed coating solution. Next, the coating solution and ferrite particles are placed in a vacuum degassing kneader and stirred at 60 ° C. for 30 minutes. Further, the carrier was prepared by degassing by depressurization while heating and drying.

[Example 1]
To 100 parts of toner particles 1-1, 0.4 part of cerium oxide (number average particle size 0.8 μm) as an external additive (conductive fine powder), and silica (number average particle size 0) as another external additive .025 μm) 3 parts was added, blended for 1 minute at a peripheral speed of 22 m / s with a Henschel mixer, coarse particles were removed using a 45 μm mesh sieve, and a toner for developing an electrostatic latent image was obtained. The liberation rate of cerium oxide in the obtained toner was 65%.
The resulting electrostatic latent image developing toner (5 parts) and the carrier (100 parts) were stirred for 20 minutes at 40 rpm using a V-blender, and sieved through a sieve having a 177 μm mesh to develop the electrostatic latent image developing toner. An agent was obtained.

  The obtained developer is put into a developing machine of a DocuCenter Color 320CP (manufactured by Fuji Xerox Co., Ltd.) remodeling machine (a remodeling machine in which the setting temperature of the fixing machine is variable), and 15000 sheets of running are fixed at 150 fixing temperatures. After setting at 0 ° C., the surface of the photoreceptor was observed. No filming was observed on the photoreceptor.

[Example 2]
An electrostatic latent image developing toner was obtained in the same manner except that the toner particles 1-1 used in Example 1 were changed to the toner particles 1-2. Incidentally, the liberation rate of cerium oxide in the obtained toner was 54%.
Further, a developer for developing an electrostatic latent image was obtained in the same manner as in Example 1, and after running 15000 sheets using the same remodeling machine, the surface of the photoreceptor was observed. Slight filming was observed on the photoreceptor.

Example 3
An electrostatic latent image developing toner was obtained by the same method except that the toner particles 1-1 used in Example 1 were changed to the toner particles 1-3. Incidentally, the liberation rate of cerium oxide in the obtained toner was 76%.
Further, a developer for developing an electrostatic latent image was obtained in the same manner as in Example 1, and after running 15000 sheets using the same remodeling machine, the surface of the photoreceptor was observed. Slight filming was observed on the photoreceptor.

[Comparative Example 1]
An electrostatic latent image developing toner was obtained in the same manner except that the toner particles 1-1 used in Example 1 were changed to the toner particles 1-4. The liberation rate of cerium oxide in the obtained toner was 48%.
Further, a developer for developing an electrostatic latent image was obtained in the same manner as in Example 1, and after running 10,000 sheets using a similar remodeling machine, the surface of the photoreceptor was observed. Filming was observed on the photoreceptor.

[Comparative Example 2]
An electrostatic latent image developing toner was obtained in the same manner except that the toner particles 1-1 used in Example 1 were changed to the toner particles 1-5. The liberation rate of cerium oxide in the obtained toner was 93%.
Further, a developer for developing an electrostatic latent image was obtained in the same manner as in Example 1, and after running 10,000 sheets using a similar remodeling machine, the surface of the photoreceptor was observed. Filming was observed on the photoreceptor.

[Comparative Example 3]
An electrostatic latent image developing toner was obtained by the same method except that the toner particles 1-1 used in Example 1 were changed to the toner particles 1-6. Note that the liberation rate of cerium oxide in the obtained toner was 95%.
Further, a developer for developing an electrostatic latent image was obtained in the same manner as in Example 1, and after running 6000 sheets using the same remodeling machine, the surface of the photoreceptor was observed. Filming was observed on the photoreceptor.

[Preparation of monodispersed spherical silica particles]
Subsequently, the silica sol obtained by the sol-gel method was subjected to HMDS treatment, and dried and pulverized to obtain spherical monodispersed silica having a sphericity Ψ = 0.85 and a volume average particle diameter D50 = 135 nm (standard deviation = 29 nm). .
The particle size of the silica particles was measured using a laser diffraction / scattering particle size distribution analyzer (HORIBA LA-910).
The sphericity Ψ was calculated from Wadell's true sphericity (the following formula).
Degree of sphericity Ψ = A / B
A: Surface area of a sphere having the same volume as the actual particle B: Surface area of the actual particle A was calculated from the volume average particle diameter. B was substituted for the BET specific surface area using Shimadzu powder specific surface area measuring device SS-100 type.

[Preparation of Toner Particles 2-1]
Amorphous resin fine particle dispersion 1: 280 parts Colorant particle dispersion: 55 parts Release agent particle dispersion: 95 parts

A solution was obtained in which the above components were sufficiently mixed and dispersed with Ultra Turrax T50 in a round stainless steel flask.
Next, with this solution mixed, 0.1 part of aluminum sulfate is added, and after 1 minute, 0.2 part of polyaluminum chloride is added to produce core agglomerated particles, and the dispersion operation is continued using an ultra turrax. did. Further, the solution in the flask was heated to 47 ° C. with stirring in an oil bath for heating and held at 47 ° C. for 60 minutes, and then 100 parts of the amorphous resin fine particle dispersion 1 was gently added to the amorphous resin fine particles. 50 parts of dispersion 2 was added to produce core / shell aggregated particles.

Thereafter, a 0.5 mol / L sodium hydroxide aqueous solution was added to adjust the pH of the solution to 6.5, and then the stainless steel flask was sealed and heated to 98 ° C. while continuing to stir using a magnetic seal. A 3 mol / L nitric acid aqueous solution was added to adjust the pH of the solution to 4.2, and then a 0.3 mol / L citric acid aqueous solution was added to adjust the pH of the solution to 3.1, and the solution was held for 5 hours. After cooling, a blue toner was obtained.
Next, the blue toner dispersed in the solution was filtered, thoroughly washed with ion exchange water, and then subjected to solid-liquid separation by Nutsche suction filtration. This was further redispersed in 3 L of ion exchanged water at 40 ° C., and stirred and washed at 300 rpm for 15 minutes.
This was repeated five more times, and when the filtrate had a pH of 7.01 and an electrical conductivity of 15.8 μS / cm, solid-liquid separation was performed using No5A filter paper by Nutsche suction filtration. Toner particles 2-1 were obtained by vacuum drying the resulting solid for 12 hours. The number average particle size distribution index G was 1.16.

[Preparation of Toner Particles 2-2]
Crystalline resin particle dispersion: 115 parts Amorphous resin fine particle dispersion 1: 190 parts Colorant particle dispersion: 55 parts Release agent particle dispersion: 95 parts

  As an attaching step, toner particles 2-2 are prepared in the same manner as toner particles 2-1, except that 125 parts of the amorphous resin fine particle dispersion 1 and 25 parts of the amorphous resin fine particle dispersion 2 are added. Produced. The number average particle size distribution index G was 1.18.

[Preparation of Toner Particles 2-3]
Crystalline resin particle dispersion: 115 parts Amorphous resin fine particle dispersion 1: 190 parts Colorant particle dispersion: 55 parts Release agent particle dispersion: 95 parts

  As an adhesion process, except that 75 parts of the amorphous resin fine particle dispersion 1 and 75 parts of the amorphous resin fine particle dispersion 2 are added, the toner particles 2-3 are prepared in the same procedure as the toner particles 2-1. Produced. The number average particle size distribution index G was 1.21.

[Preparation of Toner Particles 2-4]
Crystalline resin particle dispersion: 115 parts Amorphous resin fine particle dispersion 1: 190 parts Colorant particle dispersion: 55 parts Release agent particle dispersion: 95 parts

  As an attaching step, toner particles 2-4 were prepared in the same procedure as toner particles 2-1, except that 140 parts of the amorphous resin fine particle dispersion 1 and 10 parts of the amorphous resin fine particle dispersion 2 were added. Produced. The number average particle size distribution index G was 1.20.

[Preparation of Toner Particles 2-5]
Crystalline resin particle dispersion: 115 parts Amorphous resin fine particle dispersion 1: 190 parts Colorant particle dispersion: 55 parts Release agent particle dispersion: 95 parts

  As an adhesion process, toner particles 2-5 were prepared in the same procedure as toner particles 2-1, except that 25 parts of the amorphous resin fine particle dispersion 1 and 125 parts of the amorphous resin fine particle dispersion 2 were added. Produced. The number average particle size distribution index G was 1.25.

Example 4
To 100 parts of toner particles 2-1, 3 parts of the above-mentioned monodispersed spherical silica as an external additive (metal oxide) is added, blended for 1 minute at a peripheral speed of 22 m / s using a Henschel mixer, and using a sieve of 45 μm mesh Coarse particles were removed to obtain a toner for developing an electrostatic latent image. The liberation rate of silica of the obtained toner was 35%.
The resulting electrostatic latent image developing toner (5 parts) and the carrier (100 parts) were stirred at 40 rpm for 20 minutes using a V-blender, and sieved through a sieve having a 177 μm mesh to develop the electrostatic latent image developing toner. An agent was obtained.

  The resulting developer was run for 20000 sheets using a remodeling machine similar to that used in Example 1, and then the surface of the photoreceptor was observed. Slight filming was observed on the photoreceptor.

Example 5
An electrostatic latent image developing toner was obtained in the same manner except that the toner particles 2-1 used in Example 4 were changed to the toner particles 2-2. Incidentally, the liberation rate of silica of the obtained toner was 45%.
Further, a developer for developing an electrostatic latent image was obtained in the same manner as in Example 1, and after running 20000 sheets using the same remodeling machine, the surface of the photoreceptor was observed. No filming was observed on the photoreceptor.

Example 6
An electrostatic latent image developing toner was obtained in the same manner except that the toner particles 2-1 used in Example 4 were changed to the toner particles 2-3. Incidentally, the liberation rate of silica of the obtained toner was 55%.
Further, a developer for developing an electrostatic latent image was obtained in the same manner as in Example 1, and after running 20000 sheets using the same remodeling machine, the surface of the photoreceptor was observed. Slight filming was observed on the photoreceptor.

[Comparative Example 4]
In the same manner as in Example 4, except that the toner particles 2-1 were changed to the toner particles 2-4 and the peripheral speed of the Henschel mixer was changed to 32 m / s for 2 minutes. An image developing toner was obtained. Incidentally, the liberation rate of silica of the obtained toner was 25%.
Further, a developer for developing an electrostatic latent image was obtained in the same manner as in Example 1, and after running 10,000 sheets using a similar remodeling machine, the surface of the photoreceptor was observed. Filming was observed on the photoreceptor.

[Comparative Example 5]
In the same manner as in Example 4, except that the toner particles 2-1 were changed to the toner particles 2-5, and the peripheral speed of the Henschel mixer was changed to 15 m / s for 1 minute. An image developing toner was obtained. Incidentally, the liberation rate of silica of the obtained toner was 70%.
Further, a developer for developing an electrostatic latent image was obtained in the same manner as in Example 1, and after running 10,000 sheets using a similar remodeling machine, the surface of the photoreceptor was observed. Filming was observed on the photoreceptor.

Claims (4)

An electrostatic latent image developing toner obtained by adding a metal oxide as an external additive to toner particles containing a binder resin and a colorant, and satisfying the following condition (b1) Toner for developing electrostatic latent image.
(B1) The liberation rate of the metal oxide is 30 to 60%. The electrostatic latent image developing toner according to claim 1, wherein the binder resin contains an aliphatic crystalline polyester resin. The toner for developing an electrostatic latent image according to claim 1, wherein a ratio of the crystalline polyester resin in the binder resin is 2 to 40% by mass. 4. The toner particle according to claim 1, wherein the toner particles have a weight average molecular weight of a binder resin in a surface portion larger than a weight average molecular weight of an internal binder resin. 5. Toner for electrostatic latent image development.