JP2011107328A - Orange toner and toner storage container using the same, orange developer and process cartridge using the same, and image forming apparatus - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an orange toner which achieves high color and image reproducibility and reduces environmental dependence of image density and a toner storage container using the same, an orange developer and a process cartridge using the same, and an image forming apparatus. <P>SOLUTION: The orange toner includes, as a binder resin, a polyester resin including a dodecenylsuccinic acid structure as a structural unit and 5-18 mass% of C.I. Pigment Orange 71. There are also provided the toner storage container using the same, the orange developer including the orange toner and the process cartridge using the same, and the image forming apparatus. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

  The present invention relates to an orange toner, a toner container using the same, an orange developer, a process cartridge using the same, and an image forming apparatus.

  A method of visualizing (developing) image information through an electrostatic charge image such as electrophotography is currently used in various fields. In electrophotography, for example, an electrostatic latent image is formed on an electrostatic latent image holding member by an electrification and exposure process (electrostatic latent image forming process), and toner is supplied to this to develop the electrostatic latent image. The developed toner image is transferred to a recording medium with or without an intermediate transfer member (transfer process), and the transferred transfer image is fixed (fixing process) for visualization. Is done.

  In the case of forming a full-color image in electrophotography, generally, three colors of a combination of yellow, magenta, and cyan, which are three primary colors of color materials, or four colors of toner with black added thereto are used. Is being reproduced. In this case, a secondary color, for example, a red image is formed by laminating yellow toner and magenta toner at an appropriate ratio.

  There is also a technique in which one of three toners of red, green, and blue is further added to these toners to improve color and image reproducibility (see, for example, Patent Documents 1 to 4). Further, the orange toner exhibits the same or higher color reproducibility as the red toner even when used instead of the red toner.

JP 2008-158151 A JP 2007-304401 A Japanese Patent Laid-Open No. 2002-156776 JP 2008-3274 A

  The present invention provides an orange toner, a toner container using the same, an orange developer, a process cartridge using the same, and an image, in which high color and image reproducibility can be obtained and the environmental dependency of the image density is suppressed It is an object to provide a forming apparatus.

  The above-mentioned subject is achieved by the present invention shown in the following <1> to <8>.

  <1> A polyester resin containing a dodecenyl succinic acid structure as a binder resin as a constituent unit, and a C.I. I. An orange toner comprising CI Pigment Orange 71.

<2> Further, a hydrocarbon wax having a melting temperature of 60 ° C. or higher and lower than 100 ° C. is included,
As the binder resin, a crystalline polyester resin is contained in the binder resin component in an amount of 1% by weight to 10% by weight, and
The orange toner according to <1>, wherein the melting temperature of the hydrocarbon wax is higher than the melting temperature of the crystalline polyester resin.

<3> Weigh 0.5 g of toner, put it in 100 g of ion-exchanged water at 30 ± 1 ° C., disperse with an ultrasonic disperser for 30 minutes, and filter, and analyze the filtrate by ion chromatography. The orange toner according to <1> or <2>, wherein the amount of Na ions and the amount of NH ₄ ions detected at the time satisfy the relationship of the following formulas (a) to (c):
0.05 mg / l ≦ (Na ion amount) ≦ 0.3 mg / l (a)
0.3 mg / l ≦ (NH ₄ ion amount) ≦ 1.0 mg / l (b)
1.0 ≦ (NH ₄ ion amount) / (Na ion amount) ≦ 5.0 (c)

  <4> An orange developer comprising the orange toner according to any one of <1> to <3> and a carrier.

<5> An electrostatic latent image holding body capable of holding an electrostatic latent image formed on the surface, and developing the electrostatic latent image held on the surface of the electrostatic latent image holding body with toner to A toner image forming unit that forms a toner image on the surface of the image carrier, and a transfer unit that transfers the toner image to a recording medium;
A toner container comprising the orange toner according to any one of <1> to <3> to be supplied to the toner image forming unit.

  <6> An electrostatic latent image holder that is detachable from the image forming apparatus and can hold an electrostatic latent image formed on a surface thereof, and contains the orange developer according to <4> and the static developer. And a toner image forming unit configured to supply the toner to an electrostatic latent image formed on the surface of the electrostatic latent image holding member to form a toner image.

  <7> An electrostatic latent image holding member capable of holding an electrostatic latent image formed on the surface, charging means for charging the surface of the electrostatic latent image holding member, and the surface of the charged electrostatic latent image holding member An electrostatic latent image forming means for forming an electrostatic latent image on the surface and containing the orange developer according to <4> and supplying the toner to the electrostatic latent image formed on the surface of the electrostatic latent image holding member And a toner image forming means for forming a toner image, a transfer means for transferring the toner image to a recording medium, and a fixing means for fixing the transfer image transferred to the recording medium. Forming equipment.

<8> An electrostatic latent image holding member capable of holding an electrostatic latent image formed on the surface, charging means for charging the surface of the electrostatic latent image holding member, and the surface of the charged electrostatic latent image holding member An electrostatic latent image forming means for forming an electrostatic latent image on the surface, and a toner image forming means for forming a toner image by supplying the toner to the electrostatic latent image formed on the surface of the electrostatic latent image holding member; A transfer unit that transfers the toner image to a recording medium; and a fixing unit that fixes the transfer image transferred to the recording medium.
An image forming apparatus comprising the process cartridge according to <6>, wherein the electrostatic latent image holding member and the toner image forming unit are detachably mounted.

  According to the invention according to <1>, it is possible to provide an orange toner capable of obtaining high color and image reproducibility and suppressing environmental dependency of image density as compared with the case where the configuration of the present invention is not provided. it can.

  According to the invention according to <2>, an orange toner having high color developability can be provided as compared with a case where the configuration of the present invention is not provided.

  According to the invention according to <3>, it is possible to provide an orange toner in which the environmental dependency of the image density is suppressed as compared with a case where the amount of residual ions in the toner is not appropriately controlled.

  According to the invention according to <4>, it is possible to provide an orange developer capable of obtaining high reproducibility of color and image and suppressing environmental dependency of image density as compared with the case where the configuration of the present invention is not provided. Can do.

  According to the invention according to <5>, the toner container that stores the orange toner that can achieve high color and image reproducibility and suppresses the environmental dependency of the image density as compared with the case where the configuration of the present invention is not provided. A container can be provided.

  According to the invention according to <6>, a process in which an orange developer containing high color and image reproducibility and suppressing environmental dependency of image density is obtained as compared with the case where the configuration of the present invention is not provided. A cartridge can be provided.

  According to the invention according to <7>, image formation using orange toner that can achieve high color and image reproducibility and suppresses the environmental dependency of image density as compared with the case where the configuration of the present invention is not provided. An apparatus can be provided.

  According to the invention according to <8>, a process in which an orange developer containing high color and image reproducibility and suppressing environmental dependency of image density is obtained as compared with the case where the configuration of the present invention is not provided. An image forming apparatus including a cartridge can be provided.

1 is a schematic configuration diagram illustrating an image forming apparatus according to an exemplary embodiment that is an example of the present invention. 1 is a schematic cross-sectional view schematically showing a basic configuration of a preferred example of a process cartridge of the present invention.

[Orange Toner]
The orange toner of the present invention contains a binder resin and a colorant, and optionally contains a release agent and other components, and further contains an external additive as necessary.

  The orange toner of the present invention will be described in detail for each component of so-called toner particles excluding the external additive, its production method, and a toner added with an external additive (hereinafter sometimes simply referred to as “external additive toner”). And the physical properties of the toner particles or the externally added toner.

<Colorant>
The orange toner of the present invention has C.I. I. One feature is that (Color Index) Pigment Orange 71 is used. C. I. Pigment Orange 71 has good color developability and is suitable as a pigment for red toner in terms of color. However, since the compatibility with the polyester resin is not so good, it easily aggregates during the production.

  When the toner is produced in a state where the pigment is aggregated, the pigment is likely to be exposed on the surface of the toner, and the charge is likely to increase particularly in a low humidity environment. Variations in charging characteristics based on variations in humidity simultaneously cause variations in image density. That is, C.I. I. When a pigment orange 71 is used as a colorant and a toner using a polyester resin as a binder resin is manufactured, the environmental dependency of the image density (the image density varies depending on the humidity) tends to increase.

  In the present invention, a polyester resin containing a dodecenyl succinic acid structure as a structural unit is used as the binder resin. I. By improving the compatibility of Pigment Orange 71 and making it difficult to aggregate, the environmental dependence of the charging characteristics of the toner is suppressed.

  In the orange toner of the present invention, the colorant includes C.I. I. In addition to Pigment Orange 71, other pigments, dyes, extender pigments, and the like may be mixed and used depending on the purpose of use. However, when two or more kinds of colorants are mixed, the color may become cloudy, and when the ratio of other colorants becomes too large, C.I. I. Since it becomes impossible to enjoy the benefits of the excellent coloring property of Pigment Orange 71, C.I. I. The ratio of Pigment Orange 71 is preferably 60% by mass or more, more preferably 80% by mass or more of the entire colorant, and all of them are C.I. I. Most preferably, it is CI Pigment Orange 71.

  Examples of extender pigments that can be used include barite powder, barium carbonate, clay, silica, white carbon, talc, and alumina white.

  Examples of the dye that can be mixed include various dyes such as basic, acidic, dispersion, and direct dyes, such as nigrosine, methylene blue, rose bengal, quinoline yellow, and ultramarine blue. Moreover, these dyes may be used alone or in combination, and further in a solid solution state. When used in a wet manufacturing method, an oil-soluble dye is preferred because the dye easily escapes into the aqueous phase. It is also preferable to use the dye after subjecting it to a treatment such as chemically hydrophobizing the dye or encapsulating with a polymer.

  C. in the orange toner of the present invention. I. The blending amount of CI Pigment Orange 71 is 5% by mass or more and 18% by mass with respect to the total mass of toner (excluding external additives, the mass of so-called toner particles; hereinafter the same applies to the case of “total mass of toner”). The range is required to be in the range of mass% or less, more preferably in the range of 6 mass% to 15 mass%, and still more preferably in the range of 7 mass% to 12 mass%. If the content is too small, the color density may become thin and sufficient color development may not be obtained. If the content is too large, the density may be too high and the color may become too dark in the low image density portion.

  The dispersion diameter of the pigment in the orange toner of the present invention is preferably in the range of 30 nm to 300 nm, and more preferably in the range of 60 nm to 200 nm. If the dispersion diameter is too small, the viscosity may be remarkably increased. If it is too large, the pigment may be exposed on the toner surface and the chargeability may deteriorate.

<Binder resin>
The orange toner of the present invention includes a polyester resin containing a dodecenyl succinic acid structure as a constituent unit as a binder resin.

(Dodecenyl succinic acid structure)
The “dodecenyl succinic acid structure” is a structural unit in a state where hydrogen of two carboxyl groups in dodecenyl succinic acid is removed, and is represented by the following structural formula.

The functional group represented by C ₁₂ H ₂₃ is a dodecenyl group, and includes one carbon-carbon double bond in a linear structure having 12 carbon atoms. The position of the double bond is not specified, and any position may be used.

  The dodecenyl succinic acid structure exists as a copolymer unit in a state of being incorporated in the skeleton of the polyester resin described later. The copolymerization ratio is preferably in the range of 3 mol% to 30 mol%, more preferably in the range of 5 mol% to 25 mol%, and in the range of 7 mol% to 20 mol% with respect to the alcohol-derived structural unit of the polyester resin. Is more preferable. If the proportion of the dodecenyl succinic acid structure is too small, it is not preferable in that the dispersibility of the colorant is deteriorated, and if too large, it is not preferable in that the resin is colored brown.

  The dodecenyl succinic acid structure may be copolymerized by the presence of dodecenyl succinic acid or its anhydride together with the polyester resin synthesis raw material during the synthesis of the polyester resin, and incorporated into the skeleton of the polyester resin.

(Polyester resin)
The binder resin of the orange toner of the present invention is mainly or entirely composed of a polyester resin containing a dodecenyl succinic acid structure as a structural unit (hereinafter sometimes simply referred to as “specific polyester resin”). In the total binder resin, the mixing ratio of the specific polyester resin is preferably 60% by mass or more, more preferably 80% by mass or more, and most preferably all of them are specific polyester resins. . If the ratio of the specific polyester resin is too small, there is a possibility that the properties specific to the polyester resin cannot be fully enjoyed.

  Resins that can be used in addition to polyester resins as binder resins include monoolefins such as ethylene, propylene, butylene, and isoprene; vinyl esters such as vinyl acetate, vinyl propionate, vinyl benzoate, and vinyl butyrate; methyl acrylate, acrylic Α-methylene aliphatic monocarboxylic esters such as phenyl acid, octyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate and dodecyl methacrylate; vinyl ethers such as vinyl methyl ether, vinyl ethyl ether and vinyl butyl ether; Amorphous resins such as homopolymers such as vinyl ketones such as vinyl methyl ketone, vinyl hexyl ketone and vinyl isopropenyl ketone; and copolymers thereof. Among these, particularly typical binder resins include polystyrene, styrene-alkyl acrylate copolymer, styrene-butadiene copolymer, styrene-maleic anhydride copolymer, polystyrene, polypropylene, and the like. Further examples include polyurethane, epoxy resin, silicone resin, polyamide, and modified rosin.

  As described above, the binder resin preferably includes a crystalline resin having crystallinity, and may include a crystalline resin and the amorphous resin. The non-crystalline specific polyester resin and the crystalline resin are preferably binder resins.

  When the crystalline resin is included, the content of the crystalline resin in the toner binder resin is preferably in the range of 1% by mass to 20% by mass, more preferably in the range of 1% by mass to 10% by mass. The range of mass% or more and 8 mass% or less is more preferable. If the content of the crystalline resin is too small, the endotherm by the crystalline resin at the time of fixing may be insufficient, and the effect using the crystalline resin may not be obtained. If the content exceeds 20% by mass, the crystalline resin in the toner The domain of the image becomes larger and the number of domains increases, so that the transparency of the formed image may deteriorate.

The content of the crystalline resin in the toner binder resin is calculated by the following method.
First, the toner is dissolved in methyl ethyl ketone (MEK) at room temperature (20 ° C. or more and 25 ° C. or less). This is because, for example, when a crystalline polyester and an amorphous resin are contained in the toner, almost only the amorphous resin is dissolved in MEK at room temperature. Therefore, the amorphous resin is contained in the MEK-soluble component. Therefore, after the dissolution, the amorphous resin is obtained from the supernatant separated by centrifugation, while the solid content after centrifugation is reduced to 65%. Crystalline polyester is obtained from the filtrated portion by heating at 60 ° C. for 60 minutes, dissolving in MEK, and filtering this with a glass filter at 60 ° C. When the temperature drops during filtration by this operation, the crystalline resin is precipitated, so that the temperature is kept fast and kept warm so that the temperature does not drop. The content of the crystalline resin is determined by measuring the amount of the crystalline polyester thus obtained.

  In this embodiment, “crystalline” of “crystalline resin” has a clear endothermic peak at the temperature rising stage, not a stepwise endothermic amount change in differential scanning calorimetry (DSC) of the resin, It means having a clear exothermic peak in the temperature lowering stage. Specifically, in differential scanning calorimetry (DSC) using a differential scanning calorimeter (device name: DSC-60 type) manufactured by Shimadzu Corporation, the temperature was raised from 0 ° C. to 150 ° C. at 10 ° C./min, After holding at 150 ° C. for 5 minutes, the temperature was lowered to 0 ° C. at −10 ° C./min, held at 0 ° C. for 5 minutes, and then raised to 150 ° C. at 10 ° C./min for the second time. In the spectrum, a “clear” endothermic peak is assumed when the temperature from the onset point to the peak top of the endothermic peak is within 15 ° C. On the other hand, when the temperature from the onset point when the temperature is lowered to the peak top of the exothermic peak is within 15 ° C. and the calorific value is 25 J / g or more, it is assumed that it is a “clear” exothermic peak.

  Further, from the viewpoint of sharp melt property, the temperature from the onset point to the peak top of the endothermic peak is preferably within 15 ° C, and more preferably within 10 ° C. Both the arbitrary point of the flat part of the baseline in the DSC curve and the point where the value obtained by differentiating the spectrum curve from the baseline to the falling peak top becomes the maximum (the point where the slope of the spectrum is the highest). The intersection of tangent lines between them is called an “onset point”. Further, the endothermic peak may show a peak having a width of 40 ° C. or more and 50 ° C. or less when the toner is used.

  On the other hand, the “amorphous resin” used as the binder resin refers to a resin that does not correspond to the crystalline resin. Specifically, in differential scanning calorimetry (DSC) using a differential scanning calorimeter (device name: DSC-60 type) manufactured by Shimadzu Corporation, ON when the temperature is increased at a rate of temperature increase of 10 ° C./min. “Amorphous” when the temperature from the set point to the peak top of the endothermic peak exceeds 15 ° C., when no clear endothermic peak is observed, or when a clear exothermic peak is not observed during cooling. To do. The method for obtaining the “onset point” in the DSC curve is the same as in the case of the “crystalline resin”.

  Specific examples of the crystalline resin include a crystalline polyester resin, a crystalline vinyl resin, and the like. From the viewpoints of adhesion to paper at the time of fixing, chargeability, and adjustment of a melting temperature within a preferable range. Crystalline polyester resins are preferred. An aliphatic crystalline polyester resin having an appropriate melting temperature is more preferable.

  Crystalline vinyl resins include amyl (meth) acrylate, hexyl (meth) acrylate, heptyl (meth) acrylate, octyl (meth) acrylate, nonyl (meth) acrylate, decyl (meth) acrylate, Undecyl (meth) acrylate, tridecyl (meth) acrylate, myristyl (meth) acrylate, cetyl (meth) acrylate, stearyl (meth) acrylate, oleyl (meth) acrylate, behenyl (meth) acrylate, etc. Examples thereof include vinyl resins using long-chain alkyl and alkenyl (meth) acrylic acid esters. In the present specification, the description “(meth) acryl” means that both “acryl” and “methacryl” are included.

(Crystalline polyester resin)
The crystalline polyester resin is synthesized from a divalent acid (dicarboxylic acid) component and a divalent alcohol (diol) component. “Crystalline polyester resin” refers to differential scanning calorimetry (DSC). , Not a step-like change in endothermic amount, but a point having a clear endothermic peak. In the case of a polymer obtained by copolymerizing other components with respect to the main chain of the crystalline polyester resin, when the other components are 50% by mass or less, this copolymer is also called a crystalline polyester resin.

  In the crystalline polyester resin, examples of the acid for becoming an acid-derived structural unit include various dicarboxylic acids. However, the dicarboxylic acid as the acid-derived structural unit is not limited to one type, and two or more types of dicarboxylic acids may be used. A dicarboxylic acid-derived structural unit may be included. Further, the dicarboxylic acid may contain a sulfonic acid group in order to improve the emulsifiability in the emulsion aggregation method.

  The “acid-derived structural unit” refers to a structural portion that was an acid component before the synthesis of the polyester resin, and an “alcohol-derived structural unit” described later refers to an alcohol component before the synthesis of the polyester resin. Refers to the component that was present.

  The dicarboxylic acid 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-tridecanediol, 1,14-tetradecanediol, 1,18-octadecanediol, 1,20-eicosanediol, Or lower alkyl esters and acid anhydrides thereof.

  Among these, those having 6 to 10 carbon atoms are preferable. In order to enhance crystallinity, these linear dicarboxylic acids are preferably used in an amount of 95 constituent mol% or more, more preferably 98 constituent mol% or more of the acid-derived structural unit. In addition, "structural mol%" refers to the percentage when each structural unit (acid-derived structural unit, alcohol-derived structural unit) in the polyester resin is 1 unit (mol).

  As the acid-derived structural unit, in addition to the aliphatic dicarboxylic acid-derived structural unit, structural components such as a dicarboxylic acid-derived structural unit having a sulfonic acid group can also be included.

  In the crystalline polyester resin, an aliphatic dialcohol is desirable as an alcohol for becoming an alcohol-derived constituent unit, such as ethylene glycol, 1,3-propanediol, 1,4-butanediol, and 1,5-pentanediol. 1,6-hexanediol, 1,7-heptanediol, 1,8-octanediol, 1,9-nonanediol, 1,10-decanediol, 1,11-dodecanediol, 1,12-undecanediol, Examples include 1,13-tridecanediol, 1,14-tetradecanediol, 1,18-octadecanediol, 1,20-eicosanediol. Among them, those having 2 to 10 carbon atoms are preferable. 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-derived structural unit.

  Other divalent dialcohols include, for example, bisphenol A, hydrogenated bisphenol A, ethylene oxide and / or propylene oxide adducts of bisphenol A, 1,4-cyclohexanediol, 1,4-cyclohexanedimethanol, diethylene glycol, propylene Examples include 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.

  In addition, monovalent acids such as acetic acid and benzoic acid, monovalent alcohols such as cyclohexanol and benzyl alcohol, benzenetricarboxylic acid, naphthalenetricarboxylic acid, etc. , And their anhydrides and their lower alkyl esters, glycerin, trimethylolethane, trimethylolpropane, and pentaerythritol can also be used in combination.

  Other monomers are not particularly limited and include conventionally known divalent carboxylic acids and divalent alcohols. 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.

  The crystalline polyester resin can be synthesized in any combination from the above monomer components using a conventionally known method, and a transesterification method, a direct polycondensation method, or the like can be used alone or in combination. it can.

  Specifically, the polymerization can be carried out at a polymerization temperature of 140 ° C. or higher and 270 ° C. or lower. The reaction system is reduced in pressure as necessary, and the reaction is carried out while removing 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 solubilizing solvent and dissolved. In the polycondensation reaction, the dissolution auxiliary solvent is distilled off. In the case where a monomer having poor compatibility exists in the copolymerization reaction, it is preferable that the monomer having poor compatibility and the monomer and the acid or alcohol to be polycondensed are condensed in advance and then polycondensed together with the main component.

  The molar ratio (acid component / alcohol component) at the time of reacting the acid component and the alcohol component varies depending on the reaction conditions and the like, and thus cannot be generally stated. 1.0 to 1.0 / 0.9. In the case of a transesterification reaction, an excessive amount of a monomer that can be distilled off under vacuum, such as ethylene glycol, propylene glycol, neopentyl glycol, and cyclohexanedimethanol, may be used.

  Catalysts that can be used in the production of crystalline polyester resins include titanium acetate, titanium propionate, titanium hexanoate, titanium octanoate and other aliphatic monocarboxylic acid titanium, titanium oxalate, titanium succinate, titanium maleate, Aliphatic titanium dicarboxylates such as titanium adipate and titanium sebacate, titanium aliphatic tricarboxylates such as titanium hexanetricarboxylate and isooctanetricarboxylic acid, titanium aliphatic polycarboxylates such as titanium octanetetracarboxylate and titanium decanetetracarboxylate , Titanium monocarboxylic acid such as titanium benzoate, titanium phthalate, titanium terephthalate, titanium isophthalate, titanium naphthalenedicarboxylate, titanium biphenyldicarboxylate, anthracenedical Aromatic dicarboxylic acid titanium such as titanium oxide; aromatic tricarboxylic acid titanium such as titanium trimellitic acid and titanium naphthalenetricarboxylate; aromatic tetracarboxylic acid titanium such as benzenetetracarboxylic acid titanium and naphthalenetetracarboxylic acid titanium; Titanium aromatic carboxylates, titanium titanates of aliphatic carboxylates and titanium aromatic carboxylates and alkali metal salts thereof, titanium halides such as dichlorotitanium, trichlorotitanium, tetrachlorotitanium, tetrabromotitanium, Tetraalkoxy titanium such as tetrabutoxy titanium (titanium tetrabutoxide), tetraoctoxy titanium, tetrastearyloxy titanium, titanium acetylacetonate, titanium diisopropoxide bisacetylacetonate, Tan triethanolaminate, titanium-containing catalysts, such as.

  However, as the catalyst, the titanium-containing catalyst or the inorganic tin-based catalyst is mainly used, and other catalysts may be mixed and used. As other catalysts, those according to the amorphous polyester resin can be used.

  The catalyst is preferably added in the range of 0.02 parts by mass or more and 1.0 parts by mass or less with respect to 100 parts by mass of the monomer component (excluding dodecenyl succinic acid) during the polymerization. However, when the catalyst is used as a mixture, the content of the titanium-containing catalyst is preferably 70% by mass or more, more preferably a titanium-containing catalyst.

  The melting temperature of the crystalline polyester resin is desirably in the range of 50 ° C. to 120 ° C., and more preferably in the range of 60 ° C. to 110 ° C. Furthermore, as will be described later, when a hydrocarbon wax is added to the orange toner, it is desirable that the melting temperature of the hydrocarbon wax be lower.

  The molecular weight of the crystalline polyester resin is preferably such that the mass average molecular weight (Mw) is in the range of from 5,000 to 100,000, more preferably from 10,000 to 50,000, as measured by the GPC method using tetrahydrofuran (THF) solubles. The number average molecular weight (Mn) is preferably in the range of 2000 to 30000, more preferably in the range of 5000 to 15000. The molecular weight distribution Mw / Mn is desirably in the range of 1.5 to 20, more preferably in the range of 2 to 5. When measuring the molecular weight, the crystalline resin is preferably dissolved by heating in a 70 ° C. hot water bath in order to increase the solubility in THF.

  The crystalline polyester resin preferably has an acid value in the range of 4 mgKOH / g to 20 mgKOH / g, and more preferably in the range of 6 mgKOH / g to 15 mgKOH / g. The hydroxyl value is preferably in the range of 3 mgKOH / g to 30 mgKOH / g, and more preferably in the range of 5 mgKOH / g to 15 mgKOH / g.

(Release agent)
The orange toner of the present invention preferably contains a release agent. The release agent used is a substance having a main maximum endothermic peak in the DSC curve measured according to ASTM D3418-8 at 60 ° C. or higher and 120 ° C. or lower and a melt viscosity of 1 mPas or higher and 50 mPas or lower at 140 ° C. It is desirable to be.

  The release agent is a DSC curve measured by a differential scanning calorimeter, and the endothermic start temperature is preferably 40 ° C. or higher, and more preferably 50 ° C. or higher. The endothermic temperature varies depending on the molecular weight distribution of the wax and the molecular weight distribution of the low molecular weight and the type and amount of polar groups of the structure.

In general, when the molecular weight is increased, the endothermic start temperature increases with the melting temperature. However, in this method, the original low melting temperature and low viscosity of the wax (release agent) are lost. Therefore, it is effective to select and remove only those having a low molecular weight from the molecular weight distribution of the wax. Examples of the method include molecular distillation, solvent fractionation, and gas chromatographic fractionation.
The DSC measurement is as described above.

  The melt viscosity of the release agent is measured with an E-type viscometer. For the measurement, an E-type viscometer (manufactured by Tokyo Keiki Co., Ltd.) equipped with an oil circulation type thermostat is used. For the measurement, a cone plate / cup combination plate having a cone angle of 1.34 degrees is used. A sample is put into the cup, the temperature of the circulation device is set to 140 ° C., an empty measurement cup and cone are set to the measurement device, and the temperature is kept constant while circulating the oil. When the temperature is stabilized, 1 g of the sample is put in the measuring cup, and the cone is left still for 10 minutes. After stabilization, rotate the cone and measure. The rotational speed of the cone is 60 rpm. The measurement is performed three times, and the average value is taken as the melt viscosity η.

  Specific examples of the release agent include hydrocarbon waxes such as polyethylene wax, polypropylene wax, polybutene wax, and paraffin wax, silicones that exhibit a softening point upon heating, oleic acid amide, erucic acid amide, and ricinoleic acid amide. , Fatty acid amides such as stearic acid amide, carnauba wax, rice wax, candelilla wax, plant wax such as tree wax and jojoba oil, animal wax such as beeswax, ester such as fatty acid ester and montanic acid ester Examples thereof include mineral and petroleum waxes such as wax, montan wax, ozokerite, ceresin, microcrystalline wax, and Fischer-Tropsch wax, and modified products thereof.

  In the present invention, it is preferable to use a hydrocarbon wax having a melting temperature of 60 ° C. or higher and lower than 100 ° C. In particular, when a crystalline polyester resin is used as the binder resin and a hydrocarbon wax is used in combination, C.I. I. Pigment Orange 71 is improved in compatibility with C.I. I. Aggregation of pigment orange 71 can be further suppressed. At this time, if the melting temperature of the hydrocarbon wax is higher than the melting temperature of the crystalline polyester resin, the crystalline polyester resin melts first at the time of fixing and is compatible with the amorphous polyester resin, so that the solubility parameter decreases. However, since the hydrocarbon wax melts, the formation of the hydrocarbon wax domain can be suppressed. I. Since the formation of the domain of Pigment Orange 71 can also be suppressed, the color developability can be further improved.

  The proportion of the crystalline polyester resin in the binder resin in this embodiment is preferably 1% by mass or more and 10% by mass or less, and more preferably 2% by mass or more and 8% by mass or less in the binder resin component. . If the ratio of the crystalline polyester resin is too large, the color developability decreases because the domain of the crystalline resin itself is formed, and conversely, if it is too small, the decrease in the solubility parameter when it is compatible with the amorphous polyester is small, Waxes and C.I. I. This is not preferable because the domain formation of CI Pigment Orange 71 cannot be suppressed and the color developability is not improved.

  The addition amount of the release agent is preferably 1 part by mass or more and 15 parts by mass or less, and more preferably 3 parts by mass or more and 10 parts by mass or less with respect to 100 parts by mass of the binder resin. If the addition amount of the release agent is too small, the effect of adding the release agent may not be exhibited. On the other hand, if it is too much, the fluidity may be extremely deteriorated and the charge distribution may be very wide.

(Other ingredients)
If necessary, inorganic or organic particles can be added to the orange toner of the present invention.

  Examples of inorganic particles that can be added include silica, hydrophobized silica, alumina, titanium oxide, calcium carbonate, magnesium carbonate, tricalcium phosphate, colloidal silica, alumina-treated colloidal silica, cationic surface-treated colloidal silica, and anion surface-treated colloidal silica. These can be used alone or in combination, and it is desirable to use colloidal silica. The particle size is preferably 5 nm or more and 100 nm or less. It is also possible to use particles having different particle sizes in combination. The particles can be added directly at the time of toner production, but it is preferable to use particles dispersed in an aqueous medium such as water using an ultrasonic disperser or the like. In the dispersion, the dispersibility can be improved by using an ionic surfactant, a polymer acid, a polymer base, or the like.

  In addition, a known material such as a charge control agent may be added to the toner. The number average particle diameter of the material added at that time is desirably 1 μm or less, and more preferably 0.01 μm or more and 1 μm or less. The number average particle diameter can be measured using, for example, a microtrack.

<Manufacture of toner particles>
The orange toner production method of the present invention may use a kneading pulverization method, a wet granulation method, or the like that is generally used. Here, as the wet granulation method, suspension polymerization method, emulsion polymerization method, emulsion polymerization aggregation method, soap-free emulsion polymerization method, non-aqueous dispersion polymerization method, in-situ polymerization method, interfacial polymerization method, emulsion dispersion granulation Method, agglomeration and coalescence method, and the like. Among these, wet granulation is preferable from the viewpoint of encapsulating the crystalline resin in the toner.
Suitable examples of the wet granulation method include known melt suspension methods, emulsion aggregation methods, and dissolution suspension methods. Hereinafter, the emulsion aggregation method will be described as an example.

  The emulsion aggregation method includes a step of forming aggregated particles in a dispersion in which resin particles (hereinafter sometimes referred to as “emulsified liquid”) are dispersed to prepare an aggregated particle dispersion (aggregation step), and the aggregated particles. It is a manufacturing method including a step of fusing the aggregated particles by heating the dispersion (fusion step). Further, before the aggregation step, the aggregated particles are dispersed (dispersion step), or between the aggregation step and the fusion step, a particle dispersion in which the particles are dispersed is added and mixed in the aggregated particle dispersion, and the aggregated particles are mixed. It may be provided with a step (attachment step) in which particles are attached to form attached particles. In the adhesion step, the particle dispersion is added to and mixed with the aggregated particle dispersion prepared in the aggregation step, and the particles are adhered to the aggregated particles to form adhered particles. Corresponds to particles newly added to the aggregated particles as viewed from the aggregated particles, and is sometimes referred to as “additional particles”.

  As the additional particles, in addition to the resin particles, release agent particles, colorant particles and the like may be used singly or in combination. There is no restriction | limiting in particular as a method of adding and mixing the said particle dispersion liquid, For example, you may carry out gradually continuously, and may carry out in steps divided into several times. By providing the adhesion step, a pseudo shell structure can be formed.

  In the toner, it is desirable to form a core-shell structure by the operation of adding the additional particles. The binder resin that is the main component of the write-once particles is a shell layer resin. If this method is used, the toner shape can be easily controlled by adjusting the temperature, the number of stirring, the pH and the like in the fusing step.

In the emulsion aggregation method, it is preferable to use a crystalline polyester resin dispersion and also to use an amorphous polyester resin dispersion. It is more preferable to include an emulsification step of emulsifying the crystalline polyester resin dispersion and the amorphous polyester resin to form emulsified particles (droplets).
In the emulsification step, the emulsified particles (droplets) of the amorphous polyester resin are prepared by mixing an aqueous medium and a mixed liquid (polymer liquid) containing the amorphous polyester resin and, if necessary, a colorant. It is formed by applying a shearing force to the solution. At that time, the viscosity of the polymer liquid can be lowered to form emulsified particles by heating to a temperature equal to or higher than the glass transition temperature of the amorphous polyester resin. Moreover, a dispersing agent can also be used. Hereinafter, such a dispersion of emulsified particles may be referred to as an “amorphous polyester resin dispersion”.

  Examples of the emulsifier used when forming the emulsified particles include a homogenizer, a homomixer, a pressure kneader, an extruder, and a media disperser. The size of the emulsified particles (droplets) of the polyester resin is preferably from 0.010 μm to 0.5 μm, more preferably from 0.05 μm to 0.3 μm, in terms of the average particle size (volume average particle size). The volume average particle size of the resin particles was measured with a Doppler scattering type particle size distribution analyzer (manufactured by Nikkiso Co., Ltd., Microtrac UPA9340).

  Moreover, since the melt viscosity of the resin at the time of emulsification is not reduced to the desired particle size, by raising the temperature using an emulsifier that can pressurize above atmospheric pressure, emulsifying in a state where the resin viscosity is lowered, An amorphous polyester resin dispersion having a desired particle size can be obtained.

  In the emulsification step, a solvent may be added to the resin in advance for the purpose of reducing the viscosity of the resin. The solvent used is not particularly limited as long as it dissolves the polyester resin, but is not limited to ketone solvents such as tetrahydrofuran (THF), methyl acetate, ethyl acetate, and methyl ethyl ketone, and benzene solvents such as benzene, toluene, and xylene. It is preferable to use ester solvents and ketone solvents such as ethyl acetate and methyl ethyl ketone.

  An alcohol solvent such as ethanol or isopropyl alcohol may be added directly to water or resin. Further, salts such as sodium chloride and potassium chloride, ammonia and the like may be added. Of these, ammonia is preferably used.

  Further, a dispersant may be added. Examples of the dispersant include water-soluble polymers such as polyvinyl alcohol, methyl cellulose, carboxymethyl cellulose, and sodium polyacrylate; sodium dodecylbenzenesulfonate, sodium octadecyl sulfate, sodium oleate, sodium laurate, and potassium stearate. Anionic surfactants; cationic surfactants such as laurylamine acetate and lauryltrimethylammonium chloride; zwitterionic surfactants such as lauryldimethylamine oxide; polyoxyethylene alkyl ether, polyoxyethylene alkylphenyl ether, polyoxy Surfactants such as nonionic surfactants such as ethylene alkylamine; tricalcium phosphate, aluminum hydroxide, calcium sulfate, calcium carbonate Include inorganic compounds such as barium carbonate. Among these, anionic surfactants are preferably used.

  The amount of the dispersant used is preferably 0.01 parts by mass or more and 20 parts by mass or less with respect to 100 parts by mass of the binder resin. However, since the dispersant often affects the chargeability, it is better not to add it as much as possible when emulsifiability can be ensured by the hydrophilicity of the polyester resin main chain, the acid value of the terminal, the amount of the hydroxyl value, and the like.

  In the emulsification step, the amorphous polyester resin is copolymerized with a dicarboxylic acid having a sulfonic acid group (that is, a suitable amount of a dicarboxylic acid-derived structural unit having a sulfonic acid group in the acid-derived structural unit). Included). The addition amount is preferably 10 mol% or less in the acid-derived constitutional unit, but when the emulsifiability can be ensured by the hydrophilicity of the polyester resin main chain, the acid value of the terminal, the hydroxyl value, etc., it is not added as much as possible. Better.

  Further, a phase inversion emulsification method may be used for forming the emulsified particles. In the phase inversion emulsification method, an amorphous polyester resin is dissolved in a solvent, a neutralizing agent and a dispersion stabilizer are added as necessary, and an aqueous medium is dropped under stirring to obtain emulsified particles. Thereafter, the solvent in the resin dispersion is removed to obtain an emulsion. At this time, the order of adding the neutralizing agent and the dispersion stabilizer may be changed.

  Examples of the solvent for dissolving the resin include formic acid esters, acetic acid esters, butyric acid esters, ketones, ethers, benzenes, and halogenated carbons. Specifically, esters such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, t-butyl such as formic acid, acetic acid, butyric acid, acetone, methyl ethyl ketone (MEK), methyl propyl ketone ( MPK), methyl ketones such as methyl isopropyl ketone (MIPK), methyl butyl ketone (MBK) and methyl isobutyl ketone (MIBK), ethers such as diethyl ether and diisopropyl ether, and heterocyclic substituents such as toluene, xylene and benzene Carbon tetrachloride, methylene chloride, 1,2-dichloroethane, 1,1,2-trichloroethane, trichloroethylene, chloroform, monochlorobenzene, dichloroethylidene, and other halogenated carbons may be used alone or in combination of two or more. Is possible . Of these, acetic acid esters, methyl ketones and ethers which are low boiling solvents are usually preferably used, and acetone, methyl ethyl ketone, acetic acid, ethyl acetate and butyl acetate are particularly preferred. It is desirable to use a solvent having a relatively high volatility so as not to remain in the resin particles. The amount of these solvents used is selected from 20% by mass to 200% by mass, and more preferably from 30% by mass to 100% by mass with respect to the resin amount.

  As the aqueous medium, ion-exchanged water is basically used, but a water-soluble solvent may be included so as not to destroy the oil droplets. Examples of water-soluble solvents include methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, t-butanol, 1-pentanol and other short carbon chain alcohols; ethylene glycol monomethyl ether, ethylene glycol mono Ethylene glycol monoalkyl ethers such as ethyl ether and ethylene glycol monobutyl ether; ethers, diols, THF, acetone and the like can be mentioned, and ethanol and 2-propanol are preferably used.

  The amount of these water-soluble solvents used is selected from 0% by mass to 100% by mass, and more preferably from 5% by mass to 60% by mass with respect to the resin amount. Further, the water-soluble solvent is not only mixed with the ion-exchanged water to be added, but may be used by adding it to the resin solution.

  Moreover, you may add a dispersing agent to an amorphous polyester resin solution and an aqueous component as needed. As the dispersant, a hydrophilic colloid is formed in an aqueous component, and in particular, cellulose derivatives such as hydroxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose; polyvinyl alcohol, polyvinyl pyrrolidone, polyacrylamide, polyacrylate, Examples thereof include synthetic polymers such as polymethacrylate, and dispersion stabilizers such as gelatin, gum arabic, and agar.

  Solid fine powders such as silica, titanium oxide, alumina, tricalcium phosphate, calcium carbonate, calcium sulfate, and barium carbonate can also be used. These dispersion stabilizers are usually added so that the concentration in the aqueous component is 0 to 20% by mass, preferably 0 to 10% by mass.

  A surfactant is also used as the dispersant. As examples of the surfactant, those according to those used in the colorant dispersion described later can be used. For example, in addition to natural surfactant components such as saponins, cationic surfactants such as alkylamine hydrochlorides / acetates, quaternary ammonium salts, glycerols, fatty acid soaps, sulfates, alkylnaphthalene sulfonates, sulfones Anionic surfactants such as acid salts, phosphoric acid, phosphate esters, sulfosuccinates and the like can be mentioned, and anionic surfactants and nonionic surfactants are preferably used. In order to adjust the pH of the emulsion, a neutralizing agent may be added. As the neutralizing agent, general acids such as nitric acid, hydrochloric acid, sodium hydroxide and ammonia, and alkalis can be used.

As a method for removing the solvent from the emulsion, a method of volatilizing the solvent from the emulsion to 15 ° C. or more and 70 ° C. or less, and a method of combining this with reduced pressure are preferably used.
In the present invention, from the viewpoint of particle size distribution and particle size controllability, it is preferable to use a method in which the solvent is removed by depressurization under heating after emulsification by a phase inversion emulsification method. In addition, when used for toner, from the viewpoint of influence on charging properties, emulsification is performed by using the hydrophilicity of the polyester resin main chain, the acid value of the terminal, the hydroxyl value, etc., without using a dispersant or surfactant as much as possible. It is preferable to control the property.

  Examples of the dispersion method of the colorant and the release agent include general dispersion such as a high-pressure homogenizer, a rotary shear homogenizer, an ultrasonic disperser, a high-pressure impact disperser, a ball mill having a medium, a sand mill, and a dyno mill. The method can be used and is not limited in any way.

  If necessary, an aqueous dispersion of these colorants can be prepared using a surfactant, or an organic solvent dispersion of these colorants can be prepared using a dispersant. Hereinafter, the dispersion of the colorant and the release agent may be referred to as “colorant dispersion” or “release agent dispersion”.

  The dispersant used for the colorant dispersion or the release agent dispersion is generally a surfactant. Examples of the surfactant include anionic surfactants such as sulfate ester, sulfonate, phosphate, and soap; cationic surfactants such as amine salt type and quaternary ammonium salt type; polyethylene glycol Suitable examples include nonionic surfactants such as polyphenols, alkylphenol ethylene oxide adducts, and polyhydric alcohols. Among these, an ionic surfactant is preferable, and an anionic surfactant and a cationic surfactant are more preferable. The nonionic surfactant may be used in combination with the anionic surfactant or the cationic surfactant. Moreover, it is preferable that it is the same polarity as the dispersing agent used for other dispersion liquids, such as a mold release agent dispersion liquid.

  Specific examples of the anionic surfactant include fatty acid soaps such as potassium laurate and sodium oleate; sulfates such as octyl sulfate and lauryl sulfate; alkylnaphthalene sulfonic acids such as lauryl sulfonate, dodecyl sulfonate and dodecyl benzene sulfonate. Sodium, naphthalenesulfonate formalin condensate, monooctylsulfosuccinate, dioctylsulfosuccinate and other sulfonates; lauryl phosphate, isopropylphosphate and other phosphate esters; dioctylsulfosuccinate sodium, etc. And sulfosuccinates such as disodium and disodium polyoxyethylene sulfosuccinate lauryl.Of these, alkylbenzene sulfonate compounds such as dodecylbenzene sulfonate and its branched products are preferred.

  Specific examples of the cationic surfactant include amine salts such as laurylamine hydrochloride and stearylamine hydrochloride; quaternary ammonium salts such as lauryltrimethylammonium chloride and dilauryldimethylammonium chloride.

  Specific examples of the nonionic surfactant include alkyl ethers such as polyoxyethylene octyl ether and polyoxyethylene lauryl ether; alkylphenyl ethers such as polyoxyethylene octylphenyl ether and polyoxyethylene nonylphenyl ether; Alkyl esters such as polyoxyethylene laurate, polyoxyethylene stearate, polyoxyethylene oleate; alkylamines such as polyoxyethylene lauryl amino ether, polyoxyethylene stearyl amino ether, polyoxyethylene oleyl amino ether; polyoxy Alkyl amides such as ethylene lauric acid amide and polyoxyethylene stearic acid amide; polyoxyethylene castor oil ether, polyoxyethylene rapeseed Vegetable oil ethers such as ether; alkanolamides such as lauric acid diethanolamide, stearic acid diethanolamide, oleic acid diethanolamide; sorbitan ester ethers such as polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monopalmitate, etc. Can be mentioned.

  The addition amount of the dispersant used is preferably 2% by mass or more and 10% by mass or less, and more preferably 5% by mass or more and 30% by mass or less with respect to the colorant or the release agent.

  The aqueous dispersion medium to be used is preferably one having few impurities such as metal ions, such as distilled water and ion exchange water, and can further contain alcohol or the like. Polyvinyl alcohol, cellulose polymer, and the like can also be added, but it is better not to use them as much as possible so that they do not remain in the toner.

  The means for preparing the dispersion of the various additives is not particularly limited, and examples thereof include a ball mill, a sand mill, and a dyno mill having a rotary shearing homogenizer and a media, as well as a colorant dispersion and a release agent. Examples of the dispersion apparatus known per se include an apparatus according to the one used for the preparation of the dispersion, and an optimum apparatus can be selected and used.

  In the aggregation step, it is preferable to use an aggregating agent in order to form aggregated particles. Examples of the flocculant used include a surfactant having a polarity opposite to that of the surfactant used in the dispersant, a general inorganic metal compound (inorganic metal salt), or a polymer thereof. The metal element constituting the inorganic metal salt has a divalent or higher charge belonging to the 2A, 3A, 4A, 5A, 6A, 7A, 8, 1B, 2B, 3B group in the periodic table (long periodic table). There is no limitation as long as it dissolves in the form of ions in the aggregation system of resin particles.

  Specific examples of usable inorganic metal salts include calcium chloride, calcium nitrate, barium chloride, magnesium chloride, zinc chloride, aluminum chloride, aluminum sulfate, and other metal salts, and polyaluminum chloride, polyaluminum hydroxide, Examples thereof include inorganic metal salt polymers such as calcium polysulfide. Among them, aluminum salts and polymers thereof are particularly preferable. In general, in order to obtain a sharper particle size distribution, even if the valence of the inorganic metal salt is divalent to monovalent, bivalent to trivalent or higher, and even to the same valence, the polymerization type inorganic metal salt weight Combined is more suitable.

  The amount of the flocculant added varies depending on the type and valence of the flocculant, but is generally in the range of 0.05% by mass to 0.1% by mass. The aggregating agent does not always remain in the toner due to outflow into an aqueous medium or formation of coarse powder during the toner forming process. In particular, when the amount of the solvent in the resin is large in the toner forming step, the solvent and the aggregating agent interact and easily flow out into the aqueous medium, so it is necessary to adjust the amount according to the amount of the remaining solvent.

  In the fusion step, the agglomeration suspension is controlled to have a pH of 5 or more and 10 or less under stirring according to the aggregation step to stop the progress of aggregation, and the glass transition temperature (Tg) or higher of the resin. The aggregated particles are fused and united by heating at a temperature equal to or higher than the melting temperature of the crystalline resin (hereinafter, the glass transition temperature and the melting temperature are simply referred to as “Tg etc.”). . The heating time may be performed to the extent that desired coalescence is achieved, and may be performed for 0.2 hours or more and 10 hours or less. Thereafter, when the temperature is lowered to Tg or less of the resin to solidify the particles, the particle shape and surface properties change depending on the temperature lowering rate. It is preferable to lower the temperature to not more than Tg of the resin at a rate of 0.5 ° C./min or more, more preferably 1.0 ° C./min or more.

  Also, while heating at a temperature equal to or higher than the Tg of the resin, the particles are grown by adding a pH or a flocculant according to the aggregation process, and when the desired particle size is reached, 0.5 ° C. according to the case of the fusion process. It is preferable in terms of simplification of the process because the aggregation process and the fusion process can be performed simultaneously if the particle growth is stopped at the same time as solidification by lowering the temperature to below the Tg of the resin at a rate of / min. It may be difficult to make the aforementioned core-shell structure.

  After completing the fusing step, the particles are washed and dried to obtain toner particles. In addition, it is preferable to perform substitution washing with ion-exchanged water, and the degree of washing is generally monitored by the electric conductivity of the filtrate, and finally the electric conductivity is set to 25 μS / cm or less. Is preferred. The washing may include a step of neutralizing ions with an acid or an alkali. The treatment with an acid preferably has a pH of 6.0 or less, and the treatment with an alkali preferably has a pH of 8.0 or more.

  The solid-liquid separation after washing is not particularly limited, but from the viewpoint of productivity, suction filtration, pressure filtration such as a filter press, and the like are preferably used. Further, the drying method is not particularly limited, but from the viewpoint of productivity, freeze drying, flash jet drying, fluidized drying, vibration fluidized drying, etc. are preferably used, and the final toner moisture content is 1% by mass or less. More preferably, drying is performed so that the content is 0.7% by mass or less.

<External toner>
The toner particles obtained as described above can be externally added and mixed with inorganic particles and organic particles as external additives as fluidity aids, cleaning aids, abrasives, and the like.

  Examples of inorganic particles that can be externally added include all particles usually used as external additives on the toner surface, such as silica, alumina, titanium oxide, calcium carbonate, magnesium carbonate, tricalcium phosphate, and cerium oxide. It is done. These inorganic particles preferably have a hydrophobic surface.

  Examples of the organic particles that can be externally added include, for example, vinyl resins such as styrene polymers, (meth) acrylic polymers, and ethylene polymers, polyester resins, silicone resins, fluorine resins, and the like on the outside of normal toner surfaces. All the particles used as an additive are mentioned.

  These external additives preferably have a primary particle size of 0.01 μm or more and 0.5 μm or less. Further, a lubricant can be added. Examples of the lubricant include fatty alcohol amides such as ethylene bisstearyl amide and oleic amide, and higher alcohols such as fatty acid metal salt unilin such as zinc stearate and calcium stearate. The primary particle size is preferably 0.5 μm or more and 8.0 μm or less.

  In addition, two or more types of inorganic particles may be used from the inorganic particles, and one of the inorganic particles may have an average primary particle size of 30 nm to 200 nm, more preferably 30 nm to 180 nm. preferable.

Specifically, silica, alumina, and titanium oxide are preferable, and it is particularly preferable to add hydrophobized silica as an essential component. In particular, it is preferable to use silica and titanium oxide in combination, or to use silica having different particle diameters in combination. It is also preferable to use organic particles having a particle size of 80 nm or more and 500 nm or less in combination. Examples of the hydrophobizing agent for hydrophobizing the external additive include known materials, such as silane coupling agents, titanate coupling agents, aluminate coupling agents, and zirconium coupling agents. Examples include silicone oil and polymer coating treatment.
The external additive is adhered or fixed to the toner surface by applying a mechanical impact force with a V-type blender, a sample mill or a Henschel mixer.

<Physical properties of orange toner>
(Quantitative control of ion species)
In the orange toner (toner particles) of the present invention, it is desirable that the amount of Na ion (Na ⁺ ) and the amount of NH ₄ ion (NH ₄ ⁺ ) are appropriately controlled.

If ions remain excessively in the toner, the charge amount decreases. In particular, since the charge amount under high humidity is further reduced, the environmental dependency (humidity dependency) of the charging characteristics is increased. The polyester resin is likely to be highly dependent on the environment of the charging characteristics due to the influence of the terminal carboxyl group, and the influence is particularly magnified in the toner produced in water.
Therefore, it is preferable to improve the environmental dependence of the charging characteristics by appropriately controlling the combination of ionic species. Specifically, it is preferable to perform the following quantitative control.

0.5 g of toner to be measured (so-called toner particles, not externally added toner) is weighed, put into 100 g of ion-exchanged water at 30 ± 1 ° C., dispersed by ultrasonic for 30 minutes, and filtered. Control is performed so that the amount of Na ions and the amount of NH ₄ ions detected when the filtrate is analyzed by ion chromatography satisfy the relationships of the following formulas (a) to (c).
0.05 mg / l ≦ (Na ion amount) ≦ 0.3 mg / l (a)
0.3 mg / l ≦ (NH ₄ ion amount) ≦ 1.0 mg / l (b)
1.0 ≦ (NH ₄ ion amount) / (Na ion amount) ≦ 5.0 (c)

Since Na ion is a strong base and has strong interaction with water molecules, the effect of suppressing the overall charge amount can be obtained. However, if the amount is too large, the charge amount is too low. On the other hand, NH ₄ ion is a weak base and has a strong interaction with the carboxylic acid of the resin, so it can suppress the action of the carboxylic acid under low humidity, and particularly suppress the increase in charge under low humidity. Can do. Such a function is considered not only in the carboxylic acid but also in a polar group such as an ester bond group of the polyester main chain, but since the interaction force is weaker than that of the carboxylic acid, I guess the effect is weak.

The above formulas (a) to (c) are more preferably the following formulas (a ′) to (c ′), respectively.
0.05 mg / l ≦ (Na ion amount) ≦ 0.2 mg / l (a ′)
0.07 mg / l ≦ (NH ₄ ion amount) ≦ 0.5 mg / l (b ′)
1.4 ≦ (NH ₄ ion amount) / (Na ion amount) ≦ 3.2 (c ′)

  In order to control the amount of ions in the toner as described above, there are a method of adding at the stage of preparing the resin dispersion, a method of adding during the manufacture of the toner, a method of adding after the toner is manufactured, etc. Is preferred.

It is important that the amount of NH ₄ ⁺ interacts with the resin carboxylic acid. Even if NH ₄ ⁺ is added in a state where Na, which is a strong base, is present, the carboxylic acid and Na are already in an interaction state, and the effects of the present invention cannot be obtained. Therefore, NH ₄ ⁺ needs to be added in the resin dispersion production stage.

The amount of toner present in the toner can be controlled by the amount of NH ₃ added during production of the resin dispersion. The material used is preferably an aqueous ammonia solution. Moreover, NH ₄ ⁺ interacting with the carboxylic acid can be removed depending on the pH. For example, the residual amount in the toner can be reduced by substituting the carboxylic acid-NH ₄ ⁺ interaction with the carboxylic acid-H ⁺ by adding an acid to the emulsion to lower the pH. In this case, the same control can be performed even when the toner is manufactured.

Further, not all NH ₄ ⁺ interacts with the carboxylic acid, but part of it interacts with polar groups such as ester groups and remains in the toner. Such a remaining amount NH ₄ ⁺ is relatively easy to volatilize, and the remaining amount can be controlled by applying a vacuum state when the toner is dried.

On the other hand, the amount of Na ⁺ is controlled by the amount added during toner production. However, if the amount of Na ⁺ is too small, the toner particle size controllability may be deteriorated. The amount of Na ⁺ added during toner production is increased, and the pH is adjusted with an acid such as nitric acid or hydrochloric acid after toner production. , Na ⁺ amount can be controlled. The material used includes sodium hydroxide and a surfactant neutralized with Na, and sodium hydroxide is preferred.

(Particle size and particle size characteristics)
The orange toner of the present invention preferably has a volume average particle size (so-called toner particle size excluding externally added toner; the same applies in this section) in the range of 4 μm to 9 μm, more preferably 4. The range is from 5 μm to 8.5 μm, and more preferably from 5 μm to 8 μm. If the particle size is too large, it will be difficult to reproduce a high-definition image. Conversely, if the particle size is too small, reverse polarity toner may be produced, which may affect the image quality such as background stains and color loss. . Of course, when each demerit can be overcome, or when these demerits do not become a problem, the thing of the particle size out of the said range may be sufficient.

Further, the orange toner of the present invention draws a cumulative distribution from the smaller diameter side for each of the divided particle size ranges (channels) with respect to the particle size distribution measured by the following method. comprising a particle size volume _{D 16v%,} 50% cumulative become a particle size volume _{D 50v%,} when the particle diameter at a cumulative 84% is defined as volume _{D 84v percent, (D 84v% / D 16v} %) ^The volume average particle size distribution index (GSDv) calculated from ^1/2 is preferably 1.15 or more and 1.30 or less, and more preferably 1.15 or more and 1.25 or less.

  The volume average particle size and the like can be measured using Multisizer II (manufactured by Beckman Coulter, Inc.) with an aperture diameter of 100 μm. In this case, the measurement is carried out after dispersing the toner in an electrolytic aqueous solution (isoton aqueous solution) (concentration: 1% by mass), adding a surfactant (trade name: Contaminone), and dispersing it for 300 seconds or more with an ultrasonic disperser. went.

As for the particle size distribution, the particle size range divided based on the particle size distribution measured using Multisizer II (number of divisions: 1.59 μm or more and 64.0 μm or less is 16 channels, and the log scale is 0.00. The channel 1 is divided into 1.59 μm and less than 2.00 μm, the channel 2 is 2.00 μm and less than 2.52 μm, the channel 3 is 2.52 μm and less than 3.175 μm. , And the lower limit log value on the left side is (log 1.59 =) 0.2, (log 2.0 =) 0.3, (log 2.52 =) 0.4,... 1.7 In other words, the cumulative distribution is subtracted from the small particle diameter side, and the particle diameter that becomes 16% cumulative is the volume D ₁₆ v, the number D ₁₆ p, and the cumulative 50%. volume particle diameter at _D 50 v ( Product mean particle size), the number _{D 50} p, a volume particle size at a cumulative 84% _{D 84} v, was defined as the number _{D 84} p.

The toner preferably has a spherical shape with a shape factor SF1 in the range of 110 to 145. When the shape is spherical within this range, transfer efficiency and image density are improved, and high-quality image formation can be performed.
The shape factor SF1 is more preferably in the range of 110 to 140.

Here, the shape factor SF1 is obtained by the following formula (II).
SF1 = (ML ² / A) × (π / 4) × 100 Formula (II)
In the above formula (II), ML represents the absolute maximum length of the toner particles, and A represents the projected area of the toner particles.

The shape factor SF1 is digitized by analyzing a microscope image or a scanning electron microscope (SEM) image with an image analyzer, and can be calculated as follows, for example. That is, an optical microscope image of toner particles dispersed on the surface of a slide glass is taken into a Luzex image analyzer through a video camera, and the maximum length and projected area of 100 or more toner particles are obtained and calculated by the above formula (II). The average value is obtained.
When the toner shape factor SF1 is smaller than 110 or exceeds 140, excellent chargeability, cleaning properties, and transferability may not be obtained over a long period of time.

  Recently, since the measurement can be easily performed, the shape factor is often measured using an FPIA-3000 manufactured by Sysmex Corporation. The FPIA-3000 optically measures about 4000 particle images, and analyzes the projection image of each particle. Specifically, first, the perimeter is calculated from the projection image of one particle (perimeter of the particle image). Next, the area of the projected image is calculated, a circle having the same area as the area is assumed, and the circumference of the circle is calculated (circumference length of the circle obtained from the equivalent circle diameter). The circularity is calculated as circularity = circumference of a circle obtained from the equivalent circle diameter / perimeter of the particle image. The closer the numerical value is to 1.0, the more spherical. The circularity is preferably 0.945 or more and 0.990 or less, and more preferably 0.950 or more and 0.975 or less. When the circularity is 0.950 or less, the transfer efficiency is lowered, and when it is 0.975 or more, the cleaning property may be lowered.

  Although there is an inter-device error, 110 of the shape factor SF1 is roughly equivalent to a circularity of 0.990 of FPIA-3000. The shape factor SF1 of 140 is substantially equivalent to the circularity of 0.945 of FPIA-3000.

[Orange developer]
The orange toner of the present invention described above is used as a one-component developer as it is, or mixed with a carrier and used as a two-component developer.

  The carrier that can be used is not particularly limited, but is preferably a resin-coated carrier (generally referred to as “coated carrier”, “resin-coated carrier”, etc.), and is coated with a nitrogen-containing resin. It is more preferable that the carrier is a different carrier. Nitrogen-containing resins suitable for clothing include acrylic resins including dimethylaminoethyl methacrylate, dimethylacrylamide, acrylonitrile, amino resins including urea, urethane, melamine, guanamine, aniline, amide resins, urethane resins, and the like. These copolymer resins may be used. Among these, urea resin, urethane resin, melamine resin, and amide resin are particularly preferable.

  As the coating resin for the carrier, two or more of the nitrogen-containing resins may be used in combination, or the nitrogen-containing resin and a resin not containing nitrogen may be used in combination. The nitrogen-containing resin may be used in the form of particles and dispersed in a resin not containing nitrogen.

In general, the carrier is required to have an appropriate electric resistance value in terms of function, and specifically, it is desirable that the electric resistance value is 10 ⁹ Ωcm or more and 10 ¹⁴ Ωcm or less. For example, when the electrical resistance value is as low as 10 ⁶ Ωcm as in an iron powder carrier, an insulating resin (volume resistivity is 10 ¹⁴ Ωcm or more) is coated, and the conductive powder is dispersed in the resin coating layer. It is desirable.

  Specific examples of the conductive powder include metals such as gold, silver and copper; carbon black; semiconductive oxides such as titanium oxide and zinc oxide; titanium oxide, zinc oxide, barium sulfate, aluminum borate and potassium titanate. The surface of powder etc. was covered with tin oxide, carbon black, metal, etc. Among these, carbon black is preferable.

  Examples of the method for forming the resin coating layer on the surface of the carrier core material include an immersion method in which a powder of the carrier core material is immersed in the solution for forming the coating layer, and a solution for forming the coating layer on the surface of the carrier core material. Spray method for spraying, fluidized bed method for spraying the solution for forming the coating layer in a state where the carrier core material is floated by flowing air, and mixing the carrier core material and the solution for forming the coating layer in a kneader coater to remove the solvent. Examples of the kneader coater method include a powder coat method in which the coating resin is made into particles and mixed at a temperature equal to or higher than the melting temperature of the coating resin and mixed in the kneader coater and cooled to coat, and the kneader coater method and the powder coat method are particularly preferable. .

For the production of the carrier, a heating kneader, a heating Henschel mixer, a UM mixer or the like may be used. Depending on the amount of the coating resin, a heating fluidized rolling bed, a heating kiln, or the like may be used.
The average film thickness of the resin coating layer formed by the above method is usually in the range of 0.1 μm to 10 μm, and more preferably 0.2 μm to 5 μm.

  The core material (carrier core material) used for the carrier is not particularly limited, and examples thereof include magnetic metals such as iron, steel, nickel, and cobalt, magnetic oxides such as ferrite and magnetite, and glass beads. When using the brush method, a magnetic metal is desirable. The number average particle diameter of the carrier core material is generally preferably 10 μm or more and 100 μm or less, and more preferably 20 μm or more and 80 μm or less.

  The mixing ratio of the orange toner of the present invention and the carrier in the two-component developer is not particularly limited and may be appropriately selected depending on the intended purpose. However, toner: carrier = 1: 100-30: A range of about 100 is preferable, and a range of about 3: 100 to 20: 100 is more preferable.

[Image forming apparatus, toner container, process cartridge]
First, the image forming apparatus of the present invention using the orange toner of the present invention will be described, and the process cartridge will be described separately with reference to the toner container of the present invention mounted on the image forming apparatus. The following image forming apparatus, toner container and process cartridge are examples, and the present invention is not limited to these examples.

<Image forming apparatus>
The image forming apparatus of the present invention includes an electrostatic latent image holding body capable of holding an electrostatic latent image formed on a surface, charging means for charging the surface of the electrostatic latent image holding body, and the charged electrostatic electrostatic image. An electrostatic latent image forming means for forming an electrostatic latent image on the surface of the latent image holding member, and the toner on the electrostatic latent image containing the orange developer of the present invention and formed on the surface of the electrostatic latent image holding member. A toner image forming means for forming a toner image by supplying a toner, a transfer means for transferring the toner image to a recording medium, and a fixing means for fixing the transfer image transferred to the recording medium. To do.

  In this embodiment, the transfer means is exemplified by an intermediate transfer type that transfers via an intermediate transfer member. A primary transfer means that primarily transfers a developed toner image to the intermediate transfer member, and an intermediate transfer member. Secondary transfer means for secondary transfer of the transferred toner image to a recording material. Furthermore, the image forming apparatus according to this embodiment includes a cleaning unit that removes toner remaining on the surface of the electrostatic latent image holding member after being transferred by the primary transfer unit.

  FIG. 1 is a schematic configuration diagram illustrating an example of an image forming apparatus according to the present embodiment. The image forming apparatus 200 includes an electrostatic latent image holding member 201, a charger 202 serving as a charging unit, an image writing device 203 serving as an electrostatic latent image forming unit, a rotary developing device 204 serving as a toner image forming unit, and a primary transfer unit. A primary transfer roll 205 as a (transfer means), a cleaning device 206 as a cleaning means by a cleaning blade, and an intermediate transfer member on which toner images of a plurality of colors are stacked on a recording paper (recording medium) P and transferred together. An intermediate transfer body 207, three support rolls 208, 209, and 210 that stretch and support the intermediate transfer body 207 together with the primary transfer roll 205, a secondary transfer roll 211 that is a secondary transfer means (transfer means), and after the secondary transfer A transport belt 212 for transporting the recording paper P, and the recording paper P transported by the transport belt 212 with two heating rolls 213 and Sandwiched between the pressure roll 214, a fixing device for fixing a toner image by heat and pressure comprise (fixing unit) 215 and are configured.

  The electrostatic latent image holding member 201 is formed in a drum shape as a whole, and has a photosensitive layer on its outer peripheral surface (drum surface). The electrostatic latent image holding member 201 is provided to be rotatable in the direction of arrow C in FIG. The charger 202 uniformly charges the surface of the electrostatic latent image holding member 201. The image writing device 203 forms an electrostatic latent image by irradiating the electrostatic latent image holding member 201 uniformly charged by the charger 202 with image-like light X.

  The rotary developing device 204 includes five developing devices 204Y, 204M, 204C, 204K, and 204R that respectively accommodate yellow, magenta, cyan, black, and orange toners. In this apparatus, since toner is used as a developer for image formation, yellow toner is used for the developing device 204Y, magenta toner is used for the developing device 204M, cyan toner is used for the developing device 204C, black toner is used for the developing device 204K, The developing unit 204R stores red toner. In this embodiment, the orange toner of the present invention is used as the red toner accommodated in the developing device 204R.

  The rotary developing device 204 is driven to rotate so that the five developing devices 204R, 204Y, 204M, 204C, and 204K sequentially approach and face the electrostatic latent image holding member 201. The toner is transferred to the electrostatic latent image to form a toner image.

  Here, the developing devices other than the developing device 204R in the rotary developing device 204 may be partially removed according to the required image. For example, a rotary developing device including four developing units such as the developing unit 204Y, the developing unit 204M, the developing unit 204C, and the developing unit 204R may be used. Further, these developing devices may be used after being converted into a developing device containing a developer of a desired color such as blue or green.

  The primary transfer roll 205 sandwiches the intermediate transfer member 207 with the electrostatic latent image holding member 201 and transfers the toner image formed on the surface of the electrostatic latent image holding member 201 to the endless belt-like intermediate transfer member 207. Transfer (primary transfer) to the outer peripheral surface. The cleaning device 206 cleans (removes) toner or the like remaining on the surface of the electrostatic latent image holding member 201 after transfer. The intermediate transfer body 207 has an inner peripheral surface stretched by a plurality of support rolls 208, 209, 210 and a primary transfer roll 205, and is supported so as to be able to go around in the arrow D direction and the opposite direction. The secondary transfer roll 211 is a toner transferred to the outer peripheral surface of the intermediate transfer body 207 while sandwiching a recording sheet (recording medium) P conveyed in the direction of arrow E by a sheet conveying means (not shown) with the support roll 210. The image is transferred to the recording paper P (secondary transfer).

  The image forming apparatus 200 sequentially forms a toner image on the surface of the electrostatic latent image holding member 201 and transfers it onto the outer peripheral surface of the intermediate transfer member 207, and operates as follows. That is, first, the electrostatic latent image holding member 201 is driven to rotate, and the surface of the electrostatic latent image holding member 201 is uniformly charged by the charger 202 (charging process), and then the electrostatic latent image holding member 201 is charged. Is irradiated with image light from the image writing device 203 to form an electrostatic latent image.

(Latent image forming step).
The electrostatic latent image is developed by, for example, a red developing device 204R (development process), and then the toner image is transferred to the outer peripheral surface of the intermediate transfer member 207 by the primary transfer roll 205 (primary transfer process). At this time, orange toner or the like remaining on the surface of the electrostatic latent image holding member 201 without being transferred to the intermediate transfer member 207 is cleaned by the cleaning device 206.

  Further, the intermediate transfer member 207 having the orange toner image formed on the outer peripheral surface temporarily moves in the direction opposite to the arrow D direction while holding the orange toner image on the outer peripheral surface (at this time, static The electrostatic latent image holding member 201 and the intermediate transfer member 207 are separated from each other.) Next, for example, a position where a yellow toner image, for example, is laminated and transferred onto an orange toner image. Prepared for.

  Thereafter, with respect to each toner of yellow, magenta, cyan, and black, similarly to the above, charging by the charger 202, irradiation of image light by the image writing device 203, and formation of toner images by the developing devices 204Y, 204M, 204C, and 204K. The transfer of the toner image to the outer peripheral surface of the intermediate transfer member 207 is sequentially repeated.

  In the present embodiment, for example, when forming a red image, the developing unit 204Y applies the image on the electrostatic latent image holding body 201 onto the red toner image formed on the intermediate transfer body 207 through the development process and the primary transfer process. The yellow toner image formed on the toner image is transferred so as to be arranged in the primary transfer step, and then the magenta toner image formed on the electrostatic latent image holding member 201 by the developing device 204M is formed on the yellow toner image. Then, it is transferred so as to be arranged in the primary transfer step.

  When the transfer of the three color toner images to the outer peripheral surface of the intermediate transfer member 207 is thus completed, the toner images are collectively transferred to the recording paper P by the secondary transfer roll 211 (secondary transfer step). As a result, a recording image in which a magenta toner image, a yellow toner image, and an orange toner image are laminated in order from the image forming surface is obtained on the image forming surface of the recording paper P. After the toner image is transferred onto the surface of the recording paper P by the secondary transfer roll 211, the toner image transferred by the fixing device 215 is heated and fixed (fixing step).

  Hereinafter, a charging unit, an electrostatic latent image holder, an electrostatic latent image forming unit, a toner image forming unit, a transfer unit, an intermediate transfer member, a cleaning unit, a fixing unit, and a recording medium in the image forming apparatus 200 of FIG. 1 will be described. .

(Charging means)
For example, a charging device such as a corotron is used as the charging device 202 as the charging means, but a conductive or semiconductive charging roll may be used. A contact charger using a conductive or semiconductive charging roll may apply a direct current or an alternating current applied to the electrostatic latent image holding member 201. For example, the charger 202 charges the surface of the electrostatic latent image holding member 201 by generating a discharge in a minute space near the contact portion with the electrostatic latent image holding member 201.

  The surface of the electrostatic latent image holding member 201 is usually charged to −300 V or more and −1000 V or less by the charging unit. The conductive or semiconductive charging roll may have a single layer structure or a multiple structure. Further, a mechanism for cleaning the surface of the charging roll may be provided.

(Electrostatic latent image carrier)
The electrostatic latent image holding member 201 has a function of forming a latent image (electrostatic charge image). As the electrostatic latent image holding member, an electrophotographic photosensitive member is preferable. The electrostatic latent image holding member 201 is formed by forming a photosensitive layer including an organic photosensitive layer on the outer peripheral surface of a cylindrical conductive substrate. In general, the photosensitive layer has an undercoat layer formed on the surface of the substrate as necessary, and further includes a charge generation layer containing a charge generation material and a charge transport layer containing a charge transport material in this order. It is. The order of stacking the charge generation layer and the charge transport layer may be reversed.

  These are laminated photoreceptors in which a charge generation material and a charge transport material are contained in separate layers (charge generation layer, charge transport layer), but both the charge generation material and the charge transport material are the same. A single layer type photoreceptor included in the layer may be used, and a laminated type photoreceptor is preferable. Further, an intermediate layer may be provided between the undercoat layer and the photosensitive layer. In addition to the organic photosensitive layer, other types of photosensitive layers such as an amorphous silicon photosensitive film may be used.

(Electrostatic latent image forming means)
The image writing device 203 which is an electrostatic latent image forming unit is not particularly limited. For example, a light source such as semiconductor laser light, LED light, liquid crystal shutter light, or the like is provided on the surface of the electrostatic latent image holder. Examples of the optical system apparatus that exposes the light in the same manner.

(Toner image forming means)
The toner image forming unit has a function of developing a latent image formed on the electrostatic latent image holding member with a toner image forming agent containing toner to form a toner image. Such a toner image forming unit is not particularly limited as long as it has the above-described function, and may be appropriately selected according to the purpose. For example, a toner for developing an electrostatic charge image may be a brush, a roller or the like. For example, a known developing device having a function of attaching to the electrostatic latent image holding member 201 may be used. At the time of development, a DC voltage is normally used for the electrostatic latent image holding member 201, but an AC voltage may be further superimposed and used.

(Transfer means)
As the transfer means (in this embodiment, both the primary transfer means and the secondary transfer means), for example, a charge having a polarity opposite to that of the toner of the toner image is applied from the back side of the recording medium, and the toner is generated by electrostatic force. A transfer roll and a transfer roll pressing device using a conductive roll or a semiconductive roll that transfers an image onto the surface of the recording medium or transfers the image directly in contact with the back surface of the recording medium may be used.

  A direct current may be applied to the transfer roll as a transfer current applied to the electrostatic latent image holding member, or an alternating current may be applied in a superimposed manner. Various conditions or specifications may be appropriately set for the transfer roll according to the width of the image area to be charged, the shape of the transfer charger, the opening width, the process speed (peripheral speed), and the like. Further, a single layer foam roll or the like is suitably used as a transfer roll for cost reduction.

(Intermediate transfer member)
A known intermediate transfer member may be used as the intermediate transfer member. Materials used for the intermediate transfer member include polycarbonate resin (PC), polyvinylidene fluoride (PVDF), polyalkylene phthalate, PC / polyalkylene terephthalate (PAT) blend material, ethylene tetrafluoroethylene copolymer (ETFE) / PC, ETFE / PAT, PC / PAT blend materials, and the like can be mentioned. From the viewpoint of mechanical strength, an intermediate transfer belt using a thermosetting polyimide resin is preferable.

(Cleaning means)
The cleaning means may be appropriately selected from those that employ a blade cleaning system, a brush cleaning system, and a roll cleaning system as long as they can clean residual toner on the electrostatic latent image holding member. Among these, it is preferable to use a cleaning blade. Examples of the material for the cleaning blade include urethane rubber, neoprene rubber, and silicone rubber. Among them, it is particularly preferable to use a polyurethane elastic body because of its excellent wear resistance.
In addition, when using toner with high transfer efficiency, the aspect which does not use a cleaning means may be sufficient.

(Fixing means)
The fixing unit (fixing device) fixes the toner image transferred to the recording medium by heating, pressurizing, or heating / pressing. In addition to the two-roll system as in the present embodiment, a belt-roll nip system in which the heating side or the pressure side is in the form of a belt and the other in the form of a roll, and a belt-type two-belt system in which both the heating side and the pressure side are in a belt form. As for the belt, in addition to a system in which the belt is stretched by a plurality of rolls, a free belt system in which the belt is not stretched may be used. In the present invention, any type of fixing device may be used.

(recoding media)
Examples of a recording medium (recording paper) on which a toner image is transferred to form a final recording image include plain paper, an OHP sheet, and the like used for electrophotographic copying machines and printers. In order to further improve the smoothness of the image surface after fixing, it is preferable that the surface of the recording medium is as smooth as possible. For example, coated paper in which the surface of plain paper is coated with a resin, art paper for printing, etc. Preferably used.

In this embodiment, for example, the plain paper has a smoothness measured by JIS-P-8119 in the range of 15 to 80 seconds, and a basis weight measured by JIS-P-8124 is 80 g / m. ² or less. Examples of the coated paper include those having a coating layer on one side of a paper substrate and having a smoothness in the range of 150 seconds to 1000 seconds.

  While the image forming apparatus of the present invention has been described in detail with reference to the preferred embodiment, the present invention is not limited to the above embodiment. For example, in the above-described embodiment, each color latent image is formed on one electrostatic latent image holding member 201 by the rotary developing device 204 having developing units for the number of colors, and transferred to the intermediate transfer member 207 each time. Although the apparatus is illustrated, each color unit having an electrostatic latent image holding member, a charging unit, a toner image forming unit, a cleaning unit, and the like corresponding to the number of colors is arranged in parallel facing the intermediate transfer medium (physically linear The toner images of the respective colors formed by the respective units are primarily transferred to an intermediate transfer medium, sequentially stacked, and then collectively transferred to a recording medium. An image forming apparatus called a tandem method may be used.

  Further, the image forming apparatus of the present invention can add other conventionally known or not-known various configurations in addition to the components described in the above-described embodiment, and the image of the present invention is still added by the addition. As long as the configuration of the forming apparatus is provided, it is, of course, included in the scope of the present invention. For example, a charge eliminating unit can be provided as a subsequent process of the cleaning unit. The static elimination means will be outlined in the process cartridge section.

  In addition, those skilled in the art can appropriately modify the image forming apparatus of the present invention in accordance with conventionally known knowledge. Of course, such modifications are included in the scope of the present invention as long as the configuration of the image forming apparatus of the present invention is provided.

<Toner container>
In the present invention, the toner container is an electrostatic latent image holding body capable of holding an electrostatic latent image formed on the surface, and the electrostatic latent image held on the surface of the electrostatic latent image holding body with toner. A toner image forming unit that develops and forms a toner image on the surface of the electrostatic latent image holding member, and a transfer unit that transfers the toner image to a recording medium; It is characterized by containing the orange toner of the present invention to be supplied to the toner image forming means, and is generally called “toner cartridge”.

  That is, in the embodiment shown in FIG. 1, a toner container is a container containing the orange toner of the present invention to be supplied to the developing device 204R, and the orange toner is stored in a suitable container. Yes (not shown). The shape and material of such a container are not particularly limited, but are generally made of a plastic material such as polystyrene, polypropylene, polycarbonate, or ABS resin.

<Process cartridge>
In the present invention, the “process cartridge” is integrally provided with two or more of the components in the image forming apparatus, and is removable from the image forming apparatus main body for the purpose of maintenance, repair, periodic replacement of consumables, and the like. Means a collection of components. In the present invention, among the components in the image forming apparatus, the electrostatic latent image holding member and the toner image forming means are included, and other components are optional.

  FIG. 2 is a schematic cross-sectional view schematically showing a basic configuration of a preferred example of the process cartridge of the present invention. The process cartridge 300 shown in FIG. 2 includes an electrostatic latent image holding member 307, a charger (charging means) 308, a developing device (toner image forming means) 311 and a cleaning device (cleaning means) 313. An opening 318 for exposure and an opening 317 for static elimination exposure are provided, and a mounting rail 316 is further attached, and these are integrated. The developing device 311 contains the orange developer of the present invention described above.

  The process cartridge 300 is detachable from an image forming apparatus main body including a transfer device 312, a fixing device 315, and other components not shown, and constitutes an image forming apparatus together with the image forming apparatus main body. .

  Since the electrostatic latent image holding member 307, the charger (charging means) 308, and the cleaning device (cleaning means) 313 have already been described in the section of the embodiment of the image forming apparatus, details of the process cartridge are omitted. The same thing can be used in 300.

  Regarding the transfer device 312 for transferring the toner image developed on the surface of the electrostatic latent image holding member 307 to the recording paper 500, both the primary transfer unit and the secondary transfer unit are collectively described in the section of the embodiment of the image forming apparatus. Since the contents described as “transfer means” are also applied to the process cartridge 300 as they are, details are omitted.

  Examples of the static eliminator (light static eliminator) (not shown) include tungsten lamps and LEDs. Examples of the light quality used in the photostatic process include white light such as tungsten lamps and red light such as LED light. Is mentioned. The intensity of irradiation light in the light neutralization process is usually set to output several times to about 30 times the amount of light indicating the half exposure sensitivity of the electrostatic latent image carrier.

  In the process cartridge 300 of this example, light from such a light neutralizing device is taken in through the opening 317, and the surface of the electrostatic latent image holding member 307 is neutralized.

  On the other hand, image-like exposure light from an exposure apparatus (exposure means) (not shown) is taken in from the opening 318 in the process cartridge 300 of this example, and is irradiated onto the surface of the electrostatic latent image holding member 307 to be electrostatic latent. An image is formed.

  The process cartridge 300 shown in FIG. 2 includes a charger 308, a cleaning device 313, an opening 318 for exposure, and an opening 317 for static elimination exposure, in addition to the electrostatic latent image holding member 307 and the developing device 311. However, in the present invention, these devices and the like can be selectively combined. In the process cartridge of the present invention, the electrostatic latent image holding member and the development image forming means such as the developing device 311 are essential components, and the other components are optional elements.

  Such a process cartridge of the present invention is mounted on the above-described image forming apparatus (preferably, a so-called tandem image forming apparatus), and is an orange developing device that exhibits excellent actions and effects based on the present invention. By containing the agent, high color and image reproducibility can be obtained, and the environment dependency of the image density is suppressed.

  Hereinafter, although an example and a comparative example are given and the present invention is explained more concretely in detail, the present invention is not limited to the following examples. Unless otherwise specified, all “parts” and “%” are based on mass.

<Method for measuring ion content>
The amount of Na ions and NH ₄ ions in the toner were measured as follows.
First, 0.5 g of toner to be measured (so-called toner particles, not externally added toner) is weighed, and 0.1 g of a nonionic surfactant (nonipol manufactured by Sanyo Kasei Co., Ltd.) corresponding to 20% of the toner solid content. 10) was added to 100 g of ion-exchanged water, and the mixture was dispersed for 30 minutes in an ultrasonic disperser in a thermostat controlled at 30 ± 1 ° C.

  The liquid after ultrasonic shaking was separated into solid and liquid by suction filtration to remove solid toner, and the obtained filtrate was measured by ion chromatography. The ion chromatograph method was analyzed under the following conditions using ICS-2000 manufactured by Nippon Dionex Corporation.

Cation separation column: Nippon Dionex Co., Ltd., IonPacCS12A
Cation guard column: Nippon Dainex Co., Ltd., IonPacCG12A
Eluent: Methanesulfonic acid 20 mM
Flow rate: 1 ml / min
Temperature: 35 ° C
Detection method: Electrical conductivity method (suppressor type)

<Measurement of acid value>
The acid value AV was measured by a neutralization titration method according to JIS K0070. That is, an appropriate amount of a sample is taken, 100 ml of a solvent (diethyl ether / ethanol mixed solution) and a few drops of an indicator (phenolphthalein solution) are added, and shaken sufficiently until the sample is completely dissolved in a water bath. This was titrated with a 0.1 mol / l potassium hydroxide ethanol solution, and the end point was when the indicator was light red for 30 seconds.

  When the acid value is A, the sample amount is S (g), the 0.1 mol / l potassium hydroxide ethanol solution used for the titration is B (ml), and f is the factor of the 0.1 mol / l potassium hydroxide ethanol solution. , A = (B × f × 5.611) / S.

<Measuring method of glass transition temperature and melting temperature>
The glass transition temperature and melting temperature were measured by differential scanning calorimetry based on ASTM D3418-8. This measurement was performed as follows.

  That is, first, a substance to be measured is set in a differential scanning calorimeter (device name: DSC-50 type) manufactured by Shimadzu Corporation equipped with an automatic tangential processing system, liquid nitrogen is set as a cooling medium, and 10 ° C / Heating from 20 ° C. to 150 ° C. at a temperature rising rate of 1 minute (first temperature rising process), the relationship between temperature (° C.) and calorie (mW) was determined, The mixture was cooled to 0 ° C., and again heated to 150 ° C. at a temperature increase rate of 10 ° C./min (second temperature increase process), and data was collected. In addition, it hold | maintained for 5 minutes each at 0 degreeC and 150 degreeC. The endothermic peak temperature in the second temperature raising process was regarded as the melting temperature. The crystalline resin may show a plurality of melting peaks, but the maximum peak was regarded as the melting temperature.

  The melting temperature of the mixture of indium and zinc was used for temperature correction of the detection part of the measuring device, and the heat of fusion of indium was used for correction of the amount of heat. The sample was placed in an aluminum pan, and an aluminum pan containing the sample and an empty aluminum pan for control were set.

<Measurement of mass average molecular weight (Mw)>
The mass average molecular weight (Mw) (polystyrene conversion) of the polyester resin is a TPCgei, SuperHM-H (6.0 mm ID × 15 cm × 2) column using a GLC device, an HLC-8120GPC, SC-8020 device manufactured by Tosoh Corporation. ), And chromatographic THF (tetrahydrofuran) manufactured by Wako Pure Chemical Industries, Ltd. was used as the eluent. As experimental conditions, the sample concentration was 0.5%, and the flow rate was 0.6 ml / min. Sample injection volume 10 μl, measurement temperature 40 ° C., calibration curve is A-500, F-1, F-10, F-80, F-380, A-2500, F-4, F-40, F-128, Made from 10 samples of F-700. The data collection interval in sample analysis was 300 ms.

<Calculation of shape factor SF1>
The shape factor of the toner was measured using FPIA 3000 (manufactured by Sysmex Corporation). A toner dispersion for measurement was prepared as follows. First, 30 ml of ion-exchanged water was put into a 100 ml beaker, and 2 drops of a surfactant (Wako Pure Chemical Industries, Ltd .: Contaminone) was dropped as a dispersant. 20 mg of toner was put in this liquid and dispersed for 3 minutes by ultrasonic dispersion to prepare a dispersion.
About the obtained toner dispersion liquid, FPIA3000 was used and the number of measurement was measured 4500, and the shape factor was calculated.

<Measurement method of toner volume average particle size>
The volume average particle diameter of the toner particles was measured using a Coulter Multisizer II type (manufactured by Beckman-Coulter). As the electrolytic solution, ISOTON-II (manufactured by Beckman Coulter, Inc.) was used.

<Measurement of toner particle size distribution>
To measure the particle size distribution index of the toner, the particle size distribution measured using the Coulter Multisizer-II type described above draws a cumulative distribution from the smaller diameter side for each divided particle size range (channel) from the smaller diameter side. , D _{16V is} the particle size that is cumulative 16% for the volume, D _{16P is} the particle size that is cumulative 16% for the number, D _{50V is} the particle size that is cumulative 50% for the volume, and the particle size is 50% cumulative for the number. D _50p is defined as D _84V , a particle diameter that is 84% cumulative with respect to volume, and D _84p is a particle diameter that is cumulative 84% with respect to number.

Using these measured values, the volume average particle size distribution index (GSD _v ) is (D _84V / D _16V ) ^1/2 and the number average particle size distribution index (GSD _p ) is (D _84p / D _16p ) ^1/2. Thus, the lower number average particle size distribution index (below GSD _p ) was calculated from (D _50P / D _16P ).

<Preparation of colorant dispersion (OR1)>
Orange pigment (Ciba Japan Co., Ltd., Orange TR (CI Pigment Orange 71)): 200 parts by mass Anionic surfactant (Daiichi Kogyo Seiyaku Co., Ltd., Neogen SC): 33 parts by mass ( 60% by mass of active ingredient (10% by mass with respect to colorant)
・ Ion exchange water: 750 parts by mass

  280 parts by mass of the ion-exchanged water and the anionic surfactant are placed in a stainless steel container whose liquid level is about 1/3 of the container height when all of the above components are added. Then, the temperature is increased to 40 ° C. and the surfactant is sufficiently dissolved, then cooled to 25 ° C., all of the orange pigment is added, and the mixture is stirred using a stirrer until there is no wet pigment, Fully degassed.

  After defoaming, the remaining ion-exchanged water was added, and the mixture was dispersed for 10 minutes at 5000 revolutions using a homogenizer (manufactured by IKA, Ultra Tarrax T50). After defoaming, the mixture was dispersed again at 6000 rpm for 10 minutes using a homogenizer, and then defoamed by stirring overnight with a stirrer. Subsequently, the dispersion liquid was dispersed at a pressure of 240 MPa using a high-pressure impact disperser ultimateizer (manufactured by Sugino Machine Co., Ltd., HJP30006). The dispersion was equivalent to 25 passes in terms of the total charge and the processing capacity of the apparatus.

The obtained dispersion was allowed to stand for 72 hours to remove precipitates, and ion exchange water was added to adjust the solid content concentration to 15% by mass. The volume average particle diameter _{D 50 V} of the resulting colorant particle in the dispersion is 165 nm, 250 nm or more coarse particles was not observed. As the volume average particle diameter D _50V , an average value of three measurement values excluding the maximum value and the minimum value out of five times measured by Microtrack was used. This colorant dispersion is designated as (M1).

<Preparation of release agent dispersion (W1)>
Hydrocarbon wax (Nippon Seiki Co., Ltd., trade name: FNP0090, melting temperature Tw = 90.2 ° C.): 270 parts by mass Anionic surfactant (Daiichi Kogyo Seiyaku Co., Ltd., Neogen RK, active ingredient amount) : 60% by mass): 13.5 parts by mass (as an active ingredient, 3.0% by mass with respect to the release agent)
-Ion exchange water: 21.6 parts by mass

The above components are mixed and the release agent is dissolved at an internal liquid temperature of 120 ° C. with a pressure discharge type homogenizer (Gorin homogenizer manufactured by Gorin Co., Ltd.), followed by dispersion treatment at a dispersion pressure of 5 MPa for 120 minutes, followed by 40 MPa for 360 minutes. And cooled to obtain a release agent dispersion (W1). The volume average particle diameter D _50v of the particles in the release agent dispersion was 225 nm. Then, ion exchange water was added and it adjusted so that solid content concentration might be 20.0 mass%.

<Preparation of release agent dispersion (W2)>
Hydrocarbon wax (manufactured by Toyo Petrolite Co., Ltd., trade name: POLYWAX725, melting temperature Tw = 102 ° C.): 270 parts by mass Anionic surfactant (Daiichi Kogyo Seiyaku Co., Ltd., Neogen RK, active ingredient amount: 60) (Mass%): 13.5 mass parts (as an active ingredient, 3.0 mass% with respect to a mold release agent)
-Ion exchange water: 21.6 parts by mass

The above components are mixed and the release agent is dissolved at an internal liquid temperature of 120 ° C. with a pressure discharge type homogenizer (Gorin homogenizer manufactured by Gorin Co., Ltd.), followed by dispersion treatment at a dispersion pressure of 5 MPa for 120 minutes, followed by 40 MPa for 360 minutes. And cooled to obtain a release agent dispersion (W2). The volume average particle diameter D _50v of the particles in this release agent dispersion is 240 nm. Then, ion exchange water was added and it adjusted so that solid content concentration might be 20.0 mass%.

<Preparation of release agent dispersion (W3)>
Hydrocarbon wax (Nippon Seiki Co., Ltd., trade name: HNP-9, melting temperature Tw = 62 ° C.): 270 parts by mass Anionic surfactant (Daiichi Kogyo Seiyaku Co., Ltd., Neogen RK, active ingredient amount) : 60% by mass): 13.5 parts by mass (as active ingredient, 3.0% by mass with respect to the release agent)
-Ion exchange water: 21.6 parts by mass

The above components are mixed and the release agent is dissolved at an internal liquid temperature of 120 ° C. with a pressure discharge type homogenizer (Gorin homogenizer manufactured by Gorin Co., Ltd.), followed by dispersion treatment at a dispersion pressure of 5 MPa for 120 minutes, followed by 40 MPa for 360 minutes. And cooled to obtain a release agent dispersion (W3). The volume average particle diameter D _50v of the particles in this release agent dispersion is 240 nm. Then, ion exchange water was added and it adjusted so that solid content concentration might be 20.0 mass%.

<Synthesis of Amorphous Polyester Resin (A1)>
-Bisphenol A ethylene oxide 2.2 mol adduct: 10 mol%
-Bisphenol A propylene oxide 2.2 mol adduct: 40 mol%
・ Terephthalic acid: 22 mol%
・ Fumaric acid: 15 mol%
-Dodecenyl succinic anhydride: 11 mol%
-Trimellitic anhydride: 2 mol%

  In a reaction vessel equipped with a stirrer, a thermometer, a condenser, and a nitrogen gas introduction tube, fumaric acid and trimellitic anhydride other than the above monomer components, and tin dioctanoate for 100 parts by mass in total of the above monomer components 0.25 part by mass was added. After reacting at 235 ° C. for 6 hours under a nitrogen gas stream, the temperature was lowered to 200 ° C., and the fumaric acid and trimellitic anhydride were added and reacted for 1 hour. The temperature was further raised to 220 ° C. over 4 hours, and polymerization was performed under a pressure of 10 kPa until a desired molecular weight was obtained, to obtain a light yellow transparent amorphous polyester resin (A1).

  The obtained amorphous polyester resin (A1) has a glass transition temperature Tg by DSC of 59 ° C., a mass average molecular weight Mw by GPC of 23,000, a number average molecular weight Mn of 7000, a softening temperature by a flow tester of 106 ° C., and an acid value. AV was 11 mgKOH / g.

<Synthesis of Amorphous Polyester Resin (B1)>
-Bisphenol A propylene oxide adduct (manufactured by Sanyo Chemical Industries, Ltd., Newpol BP-2P): 80 mol%
Bisphenol A ethylene oxide adduct (manufactured by Sanyo Chemical Industries, Ltd., New Pole BPE-20): 20 mol%
・ Terephthalic acid (reagent): 70 mol%
・ Cyclohexanedicarboxylic acid (reagent): 30 mol%

  After putting the above components into a reaction vessel equipped with a stirrer, thermometer, condenser and nitrogen gas introduction tube, and replacing the inside of the reaction vessel with dry nitrogen gas, tin dioctanoate was added to 100 parts by mass of the monomer components in total. 0.25 part by mass was added. After stirring and reacting at about 180 ° C. for about 6 hours under a nitrogen gas stream, the temperature is further raised to about 220 ° C. over 1 hour, stirring and reacting for about 7.0 hours, and the temperature is further raised to 235 ° C. Then, the pressure in the reaction vessel was reduced to 10.0 mmHg, and the reaction was allowed to stir for about 2.0 hours under reduced pressure to obtain a pale yellow transparent amorphous polyester resin (B1).

  The obtained amorphous polyester resin (B1) has a glass transition temperature Tg by DSC of 52.5 ° C., a mass average molecular weight Mw by GPC of 18000, a number average molecular weight Mn of 6300, and an acid value AV of 9.3 KOH mg / g. Met.

<Synthesis of Crystalline Polyester Resin (C1)>
1,10-dodecanedioic acid: 50 mol%
・ 1,9-nonanediol: 50 mol%

  The monomer component is placed in a reaction vessel equipped with a stirrer, a thermometer, a condenser, and a nitrogen gas introduction tube. After the inside of the reaction vessel is replaced with dry nitrogen gas, titanium tetrabutoxide (reagent) is added in 100 parts by mass of the monomer component. 0.25 part by mass was charged with respect to After stirring and reacting at 170 ° C. for 3 hours under a nitrogen gas stream, the temperature was further increased to 210 ° C. over 1 hour, the pressure inside the reaction vessel was reduced to 3 kPa, and the stirring reaction was performed for 13 hours under reduced pressure. -Soluble polyester resin (C1) was obtained.

  The obtained crystalline polyester resin (C1) had a melting temperature Tc by DSC of 73.6 ° C., a mass average molecular weight Mw by GPC of 25000, a number average molecular weight Mn of 10500, and an acid value AV of 10.1 mgKOH / g. It was.

[Example 1]
<Preparation of amorphous polyester resin particle dispersion (PA1)>
While maintaining a jacketed 3 liter reaction tank (manufactured by Tokyo Rika Kikai Co., Ltd .: BJ-30N) equipped with a condenser, thermometer, water dripping device, and anchor wings at 40 ° C. in a water circulating thermostatic chamber, A mixed solvent of 160 parts by mass of ethyl acetate and 100 parts by mass of isopropyl alcohol was added, and 300 parts by mass of the amorphous polyester resin (A1) was added thereto, and stirred and dissolved at 150 rpm using a three-one motor. The oil phase was obtained. To the stirred oil phase, 14 parts by mass of a 10% by mass aqueous ammonia solution was added dropwise for 5 minutes, and after mixing for 10 minutes, 900 parts by mass of ion-exchanged water was further added dropwise at a rate of 7 parts by mass per minute. The phase was inverted to obtain an emulsion.

Immediately, 800 parts by mass of the obtained emulsion and 700 parts by mass of ion-exchanged water were placed in a 2-liter eggplant flask and set in an evaporator (Tokyo Rika Kikai Co., Ltd.) equipped with a vacuum control unit via a trap ball. . While rotating the eggplant flask, the mixture was heated in a hot water bath at 60 ° C., and the solvent was removed by reducing the pressure to 7 kPa while paying attention to bumping. When the solvent recovery amount reached 1100 parts by mass, the pressure was returned to normal pressure, and the eggplant flask was cooled with water to obtain a dispersion. There was no solvent odor in the obtained dispersion. The volume average particle diameter D _50v of the resin particles in this dispersion was 130 nm. Then, ion-exchange water was added and it adjusted so that solid content concentration might be 20 mass%, and this was made into the amorphous polyester resin dispersion liquid (PA1).

<Preparation of additional amorphous polyester resin particle dispersion (PA1A)>
350 parts by mass of the amorphous polyester resin dispersion (PA1) is placed in a 500 ml beaker, and stirred with a magnetic stirrer at a speed that does not bite bubbles, while an anionic surfactant (manufactured by Dow Chemical Co., Ltd., 3.4 parts by weight of Dowfax 2A1) was added and stirred for 10 minutes, then adjusted to pH 3.2 with 0.3 mol / l nitric acid, and an additional amorphous polyester resin particle dispersion (PA1A) Got.

<Preparation of crystalline polyester resin dispersion (PC1)>
A jacketed 3 liter reaction tank (Tokyo Rika Kikai Co., Ltd .: BJ-30N) equipped with a condenser, a thermometer, a water dropping device, an anchor blade, 300 parts by mass of the crystalline polyester resin (PC1) and methyl ethyl ketone (solvent) ) 160 parts by mass and 100 parts by mass of isopropyl alcohol (solvent) were added, and the resin was dissolved while stirring and mixing at 100 rpm while maintaining the temperature at 70 ° C. in a water circulating thermostatic bath [solution preparation step].

  Thereafter, the stirring speed was set to 150 rpm, the water circulating thermostat was set to 66 ° C., 17 parts by mass of 10% by mass ammonia water (reagent) was added over 10 minutes, and then ion-exchanged water kept at 66 ° C. was added to 7 parts. A total of 900 parts by mass was dropped at a rate of parts by mass / min to cause phase inversion to obtain an emulsion.

Immediately, 800 parts by mass of the obtained emulsion and 700 parts by mass of ion-exchanged water were placed in a 2-liter eggplant flask and set in an evaporator (Tokyo Rika Kikai Co., Ltd.) equipped with a vacuum control unit via a trap ball. . While rotating the eggplant flask, the mixture was heated in a hot water bath at 60 ° C., and the solvent was removed by reducing the pressure to 7 kPa while paying attention to bumping. When the solvent recovery amount reached 1100 parts by mass, the pressure was returned to normal pressure, and the eggplant flask was cooled with water to obtain a dispersion. There was no solvent odor in the obtained dispersion. The volume average particle diameter D _50v of the resin particles in this dispersion was 130 nm. Then, ion-exchange water was added and it adjusted so that solid content concentration might be 20 mass%, and this was made into the crystalline polyester resin dispersion liquid (PC1).

<Preparation of aqueous aluminum sulfate solution (SA)>
-Aluminum sulfate powder (Asada Chemical Co., Ltd .: 17% aluminum sulfate): 35 parts by mass-Ion-exchanged water-1965 parts by mass The above components are charged into a 2 liter container and the precipitate disappears at 30 ° C. An aqueous aluminum sulfate solution was prepared by stirring and mixing.

<Preparation of orange toner (TC1)>
Amorphous polyester resin dispersion (PA1): 700 parts by weight Colorant dispersion (OR1): 128 parts by weight Release agent dispersion (W1): 128 parts by weight Ion-exchanged water: 300 parts by weight Anion Surfactant (Dowfax 2A1 manufactured by Dow Chemical Company): 6.5 parts by mass

  The above components were put into a 3 liter reaction vessel equipped with a thermometer, pH meter, and stirrer, and at a temperature of 25 ° C., 0.3 M nitric acid was added to adjust the pH to 3.0, and then a homogenizer (IKA Japan Co., Ltd.). 130 parts by weight of the prepared aluminum sulfate aqueous solution (SA) was added and dispersed for 6 minutes while dispersing at 5000 rpm with Ultra Tarax T50).

  Thereafter, a stirrer and a mantle heater are installed in the reaction vessel, and the temperature increase rate is 0.2 ° C./min up to a temperature of 40 ° C. while adjusting the rotation speed of the stirrer so that the slurry is sufficiently stirred. After exceeding ° C., the temperature was raised at a rate of temperature increase of 0.05 ° C./min, and the particle size was measured every 10 minutes with Multisizer II (aperture diameter: 50 μm, manufactured by Beckman-Coulter). The temperature was maintained when the volume average particle size reached 5.0 μm, and all of the additional amorphous polyester resin dispersion (PA1A) was added over 5 minutes.

  The additional amorphous polyester resin dispersion (PA1A) was added and maintained for 30 minutes, and then the pH was adjusted to 9.0 using a 4% by mass aqueous sodium hydroxide solution. Thereafter, the temperature was raised to 90 ° C. at a rate of temperature rise of 1 ° C./min while maintaining the temperature at 90 ° C. while adjusting the pH to 9.0 at every 5 ° C. When the particle shape and surface property were observed with an optical microscope and a scanning electron microscope (FE-SEM) every 15 minutes, the coalescence of the particles was confirmed at 2.0 hours. Cooled to 5 ° C. over 5 minutes.

  The cooled slurry was passed through a nylon mesh having an opening of 15 μm to remove coarse powder, and the toner slurry passed through the mesh was adjusted to pH 6.0 by adding nitric acid, and then filtered under reduced pressure with an aspirator. The toner remaining on the filter paper is crushed as finely as possible by hand, poured into ion-exchanged water of 10 times the amount of toner at a temperature of 30 ° C., stirred and mixed for 30 minutes, and then filtered under reduced pressure with an aspirator again. The degree was measured. This operation was repeated until the electrical conductivity of the filtrate reached 10 μS / cm or less, and the toner was washed.

  The washed toner was finely pulverized by a wet dry granulator (Comil) and then vacuum dried in an oven at 35 ° C. for 36 hours to obtain toner particles. To 100 parts by mass of the obtained toner particles, 1.0 part by mass of hydrophobic silica (manufactured by Nippon Aerosil Co., Ltd., RY50) was added and mixed and blended at 13000 rpm for 30 seconds using a sample mill. Thereafter, the mixture was sieved with a vibration sieve having an opening of 45 μm to obtain orange toner (TC1).

The obtained orange toner (TC1) had a volume average particle diameter D _50v of 6.0 μm and a shape factor SF1 of 0.960 (FPIA-3000, manufactured by Sysmex Corporation). When the SEM image of the toner was observed, it had a smooth surface, and no problems such as protrusion of the release agent and peeling of the surface layer were observed.

<Preparation of resin-coated carrier (C)>
Mn-Mg-Sr ferrite particles (average particle size 40 μm): 100 parts by mass Toluene: 14 parts by mass A cyclohexyl methacrylate / dimethylaminoethyl methacrylate copolymer (copolymerization weight ratio 99: 1, Mw 80,000): 2.0 parts by mass / carbon black (VXC72: manufactured by Cabot): 0.12 parts by mass

  The above components excluding the ferrite particles and glass beads (φ1 mm, equivalent to toluene) were stirred at 1200 ppm for 30 minutes using a sand mill manufactured by Kansai Paint Co., to obtain a resin coating layer forming solution. Furthermore, this resin coating layer forming solution and ferrite particles were put into a vacuum degassing type kneader, decompressed, distilled off toluene, and dried to prepare a resin-coated carrier (C).

<Preparation of orange developer (DOR1)>
After adding 40 parts by mass of the orange toner (TC1) to 500 parts by mass of the resin-coated carrier (C) and blending for 20 minutes with a V-type blender, the aggregates are removed by a vibration sieve having an aperture of 212 μm. An orange developer (DOR1) was prepared.

<Preparation of replenishment orange developer (DOR1A)>
To 20 parts by mass of the resin-coated carrier (C), 100 parts by mass of the orange toner (TC2) is added, blended for 20 minutes with a V-type blender, and then aggregates are removed by a vibrating screen having an aperture of 212 μm. A replenishing orange developer (DOR1A) was obtained.

(Example 2)
<Preparation of additional amorphous polyester resin particle dispersion (PA1A)>
The same amount of amorphous polyester resin particle dispersion for addition (PA1A) as in Example 1 was obtained in the same manner as in Example 1.

<Preparation of orange toner (TC2)>
Crystalline polyester resin dispersion (PC1): 63 parts by weight Amorphous polyester resin dispersion (PA1): 637 parts by weight Colorant dispersion (OR1): 128 parts by weight Release agent dispersion (W1) : 128 parts by mass-Ion-exchanged water: 320 parts by mass-Anionic surfactant (Dowfax2A1 manufactured by Dow Chemical Co.): 7.0 parts by mass

  The above components were put into a 3 liter reaction vessel equipped with a thermometer, pH meter, and stirrer, and at a temperature of 25 ° C., 0.3 M nitric acid was added to adjust the pH to 3.0, and then a homogenizer (IKA Japan Co., Ltd.). 125 parts by mass of the prepared aluminum sulfate aqueous solution (SA) was added and dispersed for 6 minutes while dispersing at 5000 rpm with Ultra Tarax T50).

  Thereafter, a stirrer and a mantle heater are installed in the reaction vessel, and the temperature increase rate is 0.2 ° C./min up to a temperature of 40 ° C. while adjusting the rotation speed of the stirrer so that the slurry is sufficiently stirred. After exceeding ° C., the temperature was raised at a rate of temperature increase of 0.05 ° C./min, and the particle size was measured every 10 minutes with Multisizer II (aperture diameter: 50 μm, manufactured by Beckman-Coulter). The temperature was maintained when the volume average particle size reached 5.0 μm, and all of the additional amorphous polyester resin dispersion (PA1A) was added over 5 minutes.

  The additional amorphous polyester resin dispersion (PA1A) was added and maintained for 30 minutes, and then the pH was adjusted to 9.0 using a 4% by mass aqueous sodium hydroxide solution. Thereafter, the temperature was raised to 90 ° C. at a rate of temperature rise of 1 ° C./min while maintaining the pH at 9.0 ° C. while adjusting the pH to 9.0 at every 5 ° C. in the same manner. When the particle shape and surface property were observed with an optical microscope and a scanning electron microscope (FE-SEM) every 15 minutes, coalescence of the particles was confirmed at 1.0 hour. Cooled to 5 ° C. over 5 minutes.

  The cooled slurry was passed through a nylon mesh having an opening of 15 μm to remove coarse powder, and the toner slurry passed through the mesh was adjusted to pH 6.0 by adding nitric acid, and then filtered under reduced pressure with an aspirator. The toner remaining on the filter paper is crushed as finely as possible by hand, poured into ion-exchanged water of 10 times the amount of toner at a temperature of 30 ° C., stirred and mixed for 30 minutes, and then filtered under reduced pressure with an aspirator again. The degree was measured. This operation was repeated until the electrical conductivity of the filtrate reached 10 μS / cm or less, and the toner was washed.

  The washed toner was finely pulverized by a wet dry granulator (Comil) and then vacuum dried in an oven at 35 ° C. for 36 hours to obtain toner particles. To 100 parts by mass of the obtained toner particles, 1.0 part by mass of hydrophobic silica (manufactured by Nippon Aerosil Co., Ltd., RY50) and 0.8 part by mass of hydrophobic titanium oxide (manufactured by Nippon Aerosil Co., Ltd., T805) are added, Using a sample mill, the mixture was blended at 13000 rpm for 30 seconds. Thereafter, the mixture was sieved with a vibrating sieve having an opening of 45 μm to obtain orange toner (TC2).

The obtained orange toner (TC2) had a volume average particle diameter D _50v of 6.0 μm and a shape factor SF1 of 0.960 (manufactured by Sysmex Corporation, FPIA-3000). When the SEM image of the toner was observed, it had a smooth surface, and no problems such as protrusion of the release agent and peeling of the surface layer were observed.

<Preparation of orange developer (DOR2)>
The orange developer (DOR2) was prepared in the same manner as in Example 1 except that the orange toner (TC1) was replaced with the orange toner (TC2) in <Preparation of orange developer (DOR1)> in Example 1. Got.

<Preparation of replenishment orange developer (DOR2A)>
The same procedure as in Example 1 was followed except that orange toner (TC1) was replaced with orange toner (TC2) in <Preparation of replenishment orange developer (DOR1A)> in Example 1. An agent (DOR2A) was obtained.

(Example 3)
<Preparation of additional amorphous polyester resin particle dispersion (PA1A)>
The same amount of amorphous polyester resin particle dispersion for addition (PA1A) as in Example 1 was obtained in the same manner as in Example 1.

<Preparation of orange toner (TC3)>
Crystalline polyester resin dispersion (PC1): 63 parts by weight Amorphous polyester resin dispersion (PA1): 637 parts by weight Colorant dispersion (OR1): 128 parts by weight Release agent dispersion (W1) : 128 parts by mass-Ion-exchanged water: 320 parts by mass-Anionic surfactant (Dowfax2A1 manufactured by Dow Chemical Co.): 7.0 parts by mass

  The above components were placed in a 3 liter reaction vessel equipped with a thermometer, pH meter, and stirrer, and at a temperature of 25 ° C., 0.3 M nitric acid was added to adjust the pH to 3.8, and then a homogenizer (IKA Japan Co., Ltd.). 125 parts by mass of the prepared aluminum sulfate aqueous solution (SA) was added and dispersed for 6 minutes while dispersing at 5000 rpm with Ultra Tarax T50).

  Thereafter, a stirrer and a mantle heater are installed in the reaction vessel, and the temperature increase rate is 0.2 ° C./min up to a temperature of 40 ° C. while adjusting the rotation speed of the stirrer so that the slurry is sufficiently stirred. After exceeding ° C., the temperature was raised at a rate of temperature increase of 0.05 ° C./min, and the particle size was measured every 10 minutes with Multisizer II (aperture diameter: 50 μm, manufactured by Beckman-Coulter). The temperature was maintained when the volume average particle size reached 5.0 μm, and all of the additional amorphous polyester resin dispersion (PA1A) was added over 5 minutes.

  The additional amorphous polyester resin dispersion (PA1A) was added and maintained for 30 minutes, and then the pH was adjusted to 9.0 using a 4% by mass aqueous sodium hydroxide solution. Thereafter, the temperature was raised to 90 ° C. at a rate of temperature rise of 1 ° C./min while maintaining the pH at 9.0 ° C. while adjusting the pH to 9.0 at every 5 ° C. in the same manner. When the particle shape and surface property were observed with an optical microscope and a scanning electron microscope (FE-SEM) every 15 minutes, coalescence of the particles was confirmed at 1.0 hour. Cooled to 5 ° C. over 5 minutes.

  The cooled slurry was passed through a nylon mesh having a mesh size of 15 μm to remove coarse powder, and the toner slurry that passed through the mesh was filtered under reduced pressure with an aspirator. The toner remaining on the filter paper is crushed as finely as possible by hand, poured into ion-exchanged water of 10 times the amount of toner at a temperature of 30 ° C., stirred and mixed for 30 minutes, and then filtered under reduced pressure with an aspirator again. The degree was measured. This operation was repeated until the electrical conductivity of the filtrate reached 10 μS / cm or less, and the toner was washed.

  The washed toner is finely crushed with a wet dry granulator (Comil) and then subjected to the same operation as (drying wet colored toner particles 1) described in Example 1 of JP-A-2007-199202. Thus, dry toner particles were obtained.

  To 100 parts by mass of the obtained dry toner particles, 1.0 part by mass of hydrophobic silica (manufactured by Nippon Aerosil Co., Ltd., RY50) and 0.8 part by mass of hydrophobic titanium oxide (manufactured by Nippon Aerosil Co., Ltd., T805) are added. And blended for 30 seconds at 13000 rpm using a sample mill. Thereafter, the mixture was sieved with a vibration sieve having an opening of 45 μm to obtain an orange toner (TC3).

The obtained orange toner (TC3) had a volume average particle diameter D _50v of 5.8 μm and a shape factor of 0.968 (manufactured by Sysmex Corporation, FPIA-3000). When the SEM image of the toner was observed, it had a smooth surface, and no problems such as protrusion of the release agent and peeling of the surface layer were observed.

<Preparation of orange developer (DOR3)>
The orange developer (DOR3) was prepared in the same manner as in Example 1 except that the orange toner (TC1) was replaced with the orange toner (TC3) in <Preparation of orange developer (DOR1)> in Example 1. Got.

<Preparation of replenishment orange developer (DOR3A)>
The same procedure as in Example 1 was followed except that orange toner (TC1) was replaced with orange toner (TC3) in <Preparation of replenishment orange developer (DOR1A)> in Example 1. An agent (DOR3A) was obtained.

Example 4
In Example 3, the amount of the crystalline polyester resin dispersion (PC1) used in preparing the orange toner (TC3) was changed from 63 parts by mass to 10 parts by mass, and the amount of the amorphous polyester resin dispersion (PA1) used. Was changed from 637 parts by mass to 677 parts by mass, and orange toner (TC4), orange developer (DOR4), and replenishing orange developer (DOR4A) were obtained in the same manner as in Example 3. .

The obtained orange toner (TC4) had a volume average particle diameter D _50v of 5.9 μm and a shape factor of 0.955 (manufactured by Sysmex Corporation, FPIA-3000). When the SEM image of the toner was observed, it had a smooth surface, and no problems such as protrusion of the release agent and peeling of the surface layer were observed.

(Example 5)
In Example 3, the amount of the crystalline polyester resin dispersion (PC1) used in preparing the orange toner (TC3) was changed from 63 parts by mass to 103 parts by mass, and the amount of the amorphous polyester resin dispersion (PA1) used. Were changed from 637 parts by mass to 583 parts by mass in the same manner as in Example 3 to obtain orange toner (TC5), orange developer (DOR5), and replenishment orange developer (DOR5A). .

The obtained orange toner (TC4) had a volume average particle diameter D _50v of 6.0 μm and a shape factor of 0.974 (manufactured by Sysmex Corporation, FPIA-3000). When the SEM image of the toner was observed, it had a smooth surface, and no problems such as protrusion of the release agent and peeling of the surface layer were observed.

(Example 6)
In Example 3, the same procedure as in Example 3 was followed except that the release agent dispersion (W1) used was changed to the release agent dispersion (W3). DOR6) and a replenishing orange developer (DOR6A) were obtained.

The obtained orange toner (TC6) had a volume average particle diameter D _50v of 5.7 μm and a shape factor of 0.970 (manufactured by Sysmex Corporation, FPIA-3000). When the SEM image of the toner was observed, it had a smooth surface, and no problems such as protrusion of the release agent and peeling of the surface layer were observed.

(Example 7)
In Example 3, the same procedure as in Example 3 was followed except that the release agent dispersion (W1) used was changed to the release agent dispersion (W2). DOR7) and a replenishing orange developer (DOR7A) were obtained.

The obtained orange toner (TC7) had a volume average particle diameter D _50v of 5.8 μm and a shape factor of 0.962 (manufactured by Sysmex Corporation, FPIA-3000). When the SEM image of the toner was observed, it had a smooth surface, and no problems such as protrusion of the release agent and peeling of the surface layer were observed.

(Example 8)
<Preparation of crystalline polyester resin dispersion (PC1-2)>
In the preparation of the crystalline polyester resin dispersion (PC1) of Example 1, the same operation as in Example 1 except that the 10% by mass ammonia water to be added was changed from 17 parts by mass to 20 parts by mass. A crystalline polyester resin dispersion (PC1-2) was obtained. There was no solvent odor in the obtained dispersion. The volume average particle diameter D _50v of the resin particles in this dispersion was 110 nm. Then, ion exchange water was added and it adjusted so that solid content concentration might be 20 mass%.

<Preparation of orange toner (TC8)>
In Example 3, the crystalline polyester resin dispersion (PC1) used was changed to the crystalline polyester resin dispersion (PC1-2), and the additional amorphous polyester resin dispersion (PA1A) was added. The orange toner (TC8) was prepared in the same manner as in Example 3 except that the pH adjusted using a 4 mass% sodium hydroxide aqueous solution after being held for 30 minutes was changed from pH 9.0 to pH 9.2. Obtained.

The obtained orange toner (TC8) had a volume average particle diameter D _50v of 5.8 μm and a shape factor of 0.965 (manufactured by Sysmex Corporation, FPIA-3000). When the SEM image of the toner was observed, it had a smooth surface, and no problems such as protrusion of the release agent and peeling of the surface layer were observed.

<Preparation of orange developer (DOR8)>
The orange developer (DOR8) was prepared in the same manner as in Example 1 except that the orange toner (TC1) was replaced with the orange toner (TC8) in <Preparation of orange developer (DOR1)> in Example 1. Got.

<Preparation of replenishment orange developer (DOR8A)>
The same procedure as in Example 1 was followed except that orange toner (TC1) was replaced with orange toner (TC8) in <Preparation of replenishment orange developer (DOR1A)> in Example 1. An agent (DOR8A) was obtained.

Example 9
In the preparation of the orange toner (TC9) of Example 2, the pH adjustment value before the homogenizer was changed from 3.8 to 3.0, and in addition, an additional amorphous polyester resin dispersion (PA1A) was added. After maintaining for 30 minutes, the pH adjusted with a 4% by mass aqueous sodium hydroxide solution was changed from pH 9.0 to pH 7.0, and a wet silica dispersion (Nissan Chemical Co., Ltd., Snowtex OS, solid content) was changed. An orange toner (TC9), an orange developer (DOR9) and a replenishing orange developer (DOR9A) were obtained in the same manner as in Example 2 except that 25 parts by mass of 20 mass%) was added.

The obtained orange toner (TC9) had a volume average particle diameter D _50v of 5.6 μm and a shape factor of 0.968 (manufactured by Sysmex Corporation, FPIA-3000). When the SEM image of the toner was observed, it had a smooth surface, and no problems such as protrusion of the release agent and peeling of the surface layer were observed.

(Example 10)
<Preparation of amorphous polyester resin particle dispersion (PA1-2)>
In the preparation of the amorphous polyester resin particle dispersion (PA1) of Example 1, the same operation as in Example 1 was carried out except that the 10% by mass ammonia water to be added was changed from 14 parts by mass to 17 parts by mass. Amorphous polyester resin particle dispersion (PA1-2) was obtained. There was no solvent odor in the obtained dispersion. The volume average particle diameter D _50v of the resin particles in this dispersion was 120 nm. Then, ion exchange water was added and it adjusted so that solid content concentration might be 20 mass%.

<Preparation of additional amorphous polyester resin particle dispersion (PA1-2A)>
In the operation of the additional amorphous polyester resin particle dispersion (PA1A) of Example 1, the amorphous polyester resin particle dispersion (PA1) was changed to the amorphous polyester resin particle dispersion (PA1-2). Other than that, an amorphous polyester resin particle dispersion (PA1-2A) for addition was obtained in the same manner.

<Preparation of orange toner (TC3)>
Crystalline polyester resin dispersion (PC1-2): 63 parts by mass Amorphous polyester resin dispersion (PA1-2): 637 parts by weight Colorant dispersion (OR1): 128 parts by weight Release agent dispersion Liquid (W1): 128 parts by mass-ion exchanged water: 320 parts by mass-anionic surfactant (Dowfax 2A1 manufactured by Dow Chemical Co.): 7.0 parts by mass

  The above components were put into a 3 liter reaction vessel equipped with a thermometer, a pH meter, and a stirrer, and at a temperature of 25 ° C., 0.3 M nitric acid was added to adjust the pH to 4.8, and then a homogenizer (IKA Japan Co., Ltd.). 130 parts by weight of the prepared aluminum sulfate aqueous solution (SA) was added and dispersed for 6 minutes while dispersing at 5000 rpm with Ultra Tarax T50).

  Thereafter, a stirrer and a mantle heater are installed in the reaction vessel, and the temperature increase rate is 0.2 ° C./min up to a temperature of 40 ° C. while adjusting the rotation speed of the stirrer so that the slurry is sufficiently stirred. After exceeding ° C., the temperature was raised at a rate of temperature increase of 0.05 ° C./min, and the particle size was measured every 10 minutes with Multisizer II (aperture diameter: 50 μm, manufactured by Beckman-Coulter). When the volume average particle diameter reached 5.0 μm, the temperature was maintained, and all of the additional amorphous polyester resin dispersion (PA1-2A) was added over 5 minutes.

  After adding the additional amorphous polyester resin dispersion (PA1-2A) and maintaining for 30 minutes, the pH was adjusted to 9.5 using a 4% by mass aqueous sodium hydroxide solution. Thereafter, the temperature was raised to 90 ° C. at a rate of temperature rise of 1 ° C./min while maintaining the pH at 9.5 ° C. while adjusting the pH to 9.5 every 5 ° C. in the same manner. When the particle shape and surface property were observed with an optical microscope and a scanning electron microscope (FE-SEM) every 15 minutes, coalescence of the particles was confirmed at 1.0 hour. Cooled to 5 ° C. over 5 minutes.

  The cooled slurry was passed through a nylon mesh having an opening of 15 μm to remove coarse powder, and the toner slurry that passed through the mesh was filtered under reduced pressure with an aspirator. The toner remaining on the filter paper is crushed as finely as possible by hand, poured into ion-exchanged water of 10 times the amount of toner at a temperature of 30 ° C., stirred and mixed for 30 minutes, and then filtered under reduced pressure with an aspirator again. The degree was measured. This operation was repeated until the electric conductivity of the filtrate reached 15 μS / cm or less, and the toner was washed.

  The washed toner is finely crushed with a wet dry granulator (Comil) and then subjected to the same operation as (drying wet colored toner particles 1) described in Example 1 of JP-A-2007-199202. Thus, dry toner particles were obtained.

  To 100 parts by mass of the obtained dry toner particles, 1.0 part by mass of hydrophobic silica (manufactured by Nippon Aerosil Co., Ltd., RY50) and 0.8 part by mass of hydrophobic titanium oxide (manufactured by Nippon Aerosil Co., Ltd., T805) are added. And blended for 30 seconds at 13000 rpm using a sample mill. Thereafter, the mixture was sieved with a vibration sieve having an opening of 45 μm to obtain orange toner (TC10).

The obtained orange toner (TC10) had a volume average particle diameter D _50v of 5.8 μm and a shape factor of 0.972 (manufactured by Sysmex Corporation, FPIA-3000). When the SEM image of the toner was observed, it had a smooth surface, and no problems such as protrusion of the release agent and peeling of the surface layer were observed.

<Preparation of orange developer (DOR10)>
The orange developer (DOR10) was prepared in the same manner as in Example 1 except that the orange toner (TC1) was replaced with the orange toner (TC10) in <Preparation of orange developer (DOR1)> in Example 1. Got.

<Preparation of replenishment orange developer (DOR10A)>
The same procedure as in Example 1 was followed except that orange toner (TC1) was replaced with orange toner (TC10) in <Preparation of replenishment orange developer (DOR1A)> in Example 1. An agent (DOR10A) was obtained.

(Comparative Example 1)
<Preparation of Amorphous Polyester Resin Particle Dispersion (PB1)>
Example 1 except that the amorphous polyester resin (A1) used was changed to the amorphous polyester resin (B1) in <Preparation of Amorphous Polyester Resin Particle Dispersion (PA1)> in Example 1. A dispersion was obtained in the same manner as in. The volume average particle diameter D _50v of the resin particles in this dispersion was 145 nm. Then, ion-exchange water was added and it adjusted so that solid content concentration might be 20 mass%, and this was made into the amorphous polyester resin dispersion liquid (PB1).

<Preparation of additional amorphous polyester resin particle dispersion (PB1A)>
350 parts by mass of the amorphous polyester resin dispersion (PB1) is placed in a 500 ml beaker, and stirred with a magnetic stirrer at a speed that does not entrap bubbles, an anionic surfactant (manufactured by Dow Chemical Company, After adding 3.4 parts by weight of Dowfax 2A1) and stirring for 10 minutes, the pH was adjusted to 3.6 using 0.3 mol / l nitric acid, and an additional amorphous polyester resin particle dispersion (PB1A) Got.

<Preparation of orange toner (TCC)>
In <Preparation of Orange Toner (TC1)> in Example 1, the amorphous polyester resin dispersion (PA1) was changed to an amorphous polyester resin dispersion (PB1), and an additional amorphous polyester resin particle dispersion (PA1A). ) Was changed to an additional amorphous polyester resin particle dispersion (PB1A), and orange toner (TCC) was obtained in the same manner as in Example 1.

The obtained orange toner (TCC) had a volume average particle diameter D _50v of 6.0 μm and a shape factor of 0.952 (manufactured by Sysmex Corporation, FPIA-3000). When an SEM image of the toner was observed, no irregularities such as protrusion of the release agent and peeling of the surface layer were observed, but small irregularities having a size of 100 nm to 300 nm were observed on the toner surface.

<Preparation of orange developer (DORC)>
In Example 1 <Preparation of orange developer (DOR1)>, except that orange toner (TC1) was changed to orange toner (TCC), orange developer (DORC) was prepared in the same manner as in Example 1. Obtained.

<Preparation of orange developer (DORCA)>
The orange development for replenishment was carried out in the same manner as in Example 1 except that the orange toner (TC1) was replaced with the orange toner (TCC) in <Preparation of replenishment orange developer (DOR1A)> in Example 1. An agent (DORCA) was obtained.

[Evaluation test]
The following evaluation tests were performed on the obtained orange toner, orange developer, and replenishment orange developer of Examples 1 to 7 and Comparative Example 1, respectively. The results are summarized in Table 1 below.

<Color gamut evaluation>
After removing the developer and toner set as standard in the Fuji Xerox DocuCentre Color 400 CP cyan developer and cyan toner cartridge in an environmental room at a temperature of 25 ° C. and a humidity of 60%, The prepared orange developer was put into a cyan developing device, and the replenishing orange developer was put into a cyan toner cartridge. The main body of the apparatus was thoroughly cleaned before the toner and developer were charged.

  The magenta developing unit, yellow developing unit, black developing unit, and toner cartridges of the respective colors were set at the positions where the original developing units of the DocuCenter Color 400 CP were set.

Then, 20 sheets of A3 paper were passed through without developing anything, and left in this state for 48 hours. Next, after passing 10 sheets of A3 paper without developing anything, the development toner amount of each 100% monochrome image on the OK top coat paper was adjusted to 4.0 g / m ² and 5 cm × 5 cm. A single color image consisting of 100% of only orange toner was formed.

The image density and color coordinates (L * a * b *) were measured for the obtained image. For the measurement, X-Rite 939 (aperture 4 mm) was used, and the inside of the image plane was measured 10 times at random, and the average values were set as image density (Dr) and color coordinates (Lab), respectively. Further, the color coordinates are saturation (c *) (the square root of the sum of the square of (a *) and the square of (b *)), hue angle (H) (= tan ⁻¹ (b * / a *) ). The greater the saturation (c *), the more vivid colors can be expressed.

  Next, only for magenta toner, the magenta toner cartridge was removed, and the amount of toner supplied to the developing device was set to zero. In this state, a secondary color image composed of 100% yellow toner and 100% magenta toner having a size of 5 cm × 5 cm was repeatedly formed. In this way, the magenta toner in the magenta developing device is reduced, and an image in which only 100% of the magenta toner is gradually reduced without changing the yellow 100% from the original 100% yellow and 100% magenta images is formed. did. For the obtained image, the image density and color coordinates were measured, and the hue angle (Hym) was calculated. When the calculated hue angle (Hym) has a relationship of (H) -1 degree ≦ (Hym) ≦ (H) +1 degree with the hue angle (H) of the monochrome image made of 100% of the orange toner. Was defined as an orange image composed of yellow toner and magenta toner, and saturation (c * ym) was calculated.

The saturation (c *) of the orange image was compared with the saturation (c * ym) of the orange image composed of yellow toner and magenta toner, and the color gamut (saturation) was evaluated according to the following evaluation criteria.
A: When the monochromatic image is 4 or more larger than the secondary color image O: When the monochromatic image is 2 or more and less than 4 than the secondary color image Δ: The monochromatic image is 0 or more and less than 2 than the secondary color image When large ×: When the monochrome image is smaller than the secondary color image

[Evaluation of image density under low humidity]
After the above color gamut evaluation has been completed, the developer toner amount is adjusted to 4.0 g / m ² again, the environmental correction function of the DocuCenter Color 400 CP manufactured by Fuji Xerox Co., Ltd. is turned off, and the temperature and humidity of the environmental chamber are adjusted. The temperature was set to 15 ° C. and the humidity was set to 15%. After leaving in this state for 120 hours, three sheets of A3 paper were passed through without developing anything.

  Thereafter, an image composed of only 100% orange toner having a size of 5 cm × 5 cm was formed, and the resulting image density was measured. For measurement, X-Rite 939 (aperture 4 mm) was used, and the image plane was randomly measured 10 times, and the average value was defined as the density (Dc).

The ratio of the obtained image density (Dc) to the image density (Dr) obtained at the time of color gamut evaluation (temperature 25 ° C., humidity 60%), Dc / Dr was calculated, and the following evaluation criteria The saturation was evaluated.
A: Dc / Dr is 0.97 or more and less than 1.03 B: Dc / Dr is 0.93 or more and less than 0.97, or 1.03 or more and less than 1.07 Δ: Dc / Dr is 0.9 or more and 0 .93 or less, or 1.07 or more and less than 1.10 X: Dc / Dr is less than 0.9 or 1.10 or more

[Consideration of results]
The orange toner of the example was excellent in saturation. In addition, it was confirmed that the decrease in image density was suppressed even in a low humidity environment, and the environmental dependence of the image density was suppressed.

  200: Image forming apparatus 201, 307: Electrostatic latent image holding member 202, 308: Charger (charging means) 203: Image writing apparatus (electrostatic latent image forming means) 204: Rotary developing device (toner) 204Y, 204M, 204C, 204K, 204R: developing unit, 205: primary transfer roll (transfer means), 206, 313: cleaning device, 207: intermediate transfer member, 208, 209, 210: support roll, 211: secondary transfer roll, 212: transport belt, 213: heating roll, 214: pressure roll, 215, 315: fixing device, 300: process cartridge, 311: developing device, 312: transfer device, 316: mounting rail, 317: opening, 318: opening, P: recording paper (recording medium)

Claims (8)

A polyester resin containing a dodecenyl succinic acid structure as a binder resin as a constituent unit, and a C.I. I. An orange toner comprising CI Pigment Orange 71. Furthermore, it contains a hydrocarbon wax having a melting temperature of 60 ° C. or higher and lower than 100 ° C.,
As the binder resin, a crystalline polyester resin is contained in the binder resin component in an amount of 1% by weight to 10% by weight, and
The orange toner according to claim 1, wherein a melting temperature of the hydrocarbon wax is higher than a melting temperature of the crystalline polyester resin. When 0.5 g of toner is weighed, put into 100 g of ion exchange water at 30 ± 1 ° C., dispersed for 30 minutes by an ultrasonic disperser, filtered, and the filtrate was analyzed by ion chromatography. 3. The orange toner according to claim 1, wherein the detected amount of Na ions and the amount of NH ₄ ions satisfy a relationship of the following formulas (a) to (c).
0.05 mg / l ≦ (Na ion amount) ≦ 0.3 mg / l (a)
0.3 mg / l ≦ (NH ₄ ion amount) ≦ 1.0 mg / l (b)
1.0 ≦ (NH ₄ ion amount) / (Na ion amount) ≦ 5.0 (c) An orange developer comprising the orange toner according to claim 1 and a carrier. An electrostatic latent image holding body capable of holding an electrostatic latent image formed on the surface, and the electrostatic latent image holding body by developing the electrostatic latent image held on the surface of the electrostatic latent image holding body with toner. Detachable from an image forming apparatus comprising a toner image forming means for forming a toner image on the surface and a transfer means for transferring the toner image to a recording medium;
A toner storage container containing the orange toner according to claim 1 for supplying to the toner image forming means. An electrostatic latent image holding member that is detachable from an image forming apparatus and can hold an electrostatic latent image formed on a surface thereof, and contains the orange developer according to claim 4 and the electrostatic latent image. And a toner image forming unit configured to supply the toner to an electrostatic latent image formed on the surface of the holding member to form a toner image. An electrostatic latent image holding member capable of holding an electrostatic latent image formed on the surface; charging means for charging the surface of the electrostatic latent image holding member; An electrostatic latent image forming means for forming a latent image; and the orange developer according to claim 4 and the toner supplied to the electrostatic latent image formed on the surface of the electrostatic latent image holding member An image forming apparatus comprising: a toner image forming unit that forms an image; a transfer unit that transfers the toner image to a recording medium; and a fixing unit that fixes the transfer image transferred to the recording medium. An electrostatic latent image holding member capable of holding an electrostatic latent image formed on the surface; charging means for charging the surface of the electrostatic latent image holding member; An electrostatic latent image forming unit that forms a latent image; a toner image forming unit that forms a toner image by supplying the toner to the electrostatic latent image formed on the surface of the electrostatic latent image holder; and the toner image A transfer means for transferring the image to a recording medium, and a fixing means for fixing the transfer image transferred to the recording medium,
An image forming apparatus comprising the process cartridge according to claim 6, wherein the electrostatic latent image holding member and the toner image forming unit are detachably mounted.

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