JP6204144B2 - Toner production method - Google Patents

Description

  The present invention relates to a toner and a manufacturing method thereof, and more particularly to a capsule toner and a manufacturing method thereof.

  In electrophotography, the surface of a charged photosensitive drum is exposed to form an electrostatic latent image on the surface of the photosensitive drum. Then, the electrostatic latent image is developed with toner to form a toner image. Further, the toner image is transferred to a recording medium. As a result, an image is formed on the recording medium.

  The electrostatic latent image developing toner is composed of a large number of toner particles. The toner particles are obtained through a mixing step, a kneading step, a pulverizing step, and a classification step in which components such as a colorant, a charge control agent, a release agent, and a magnetic material are mixed with the binder resin.

  The capsule toner includes a core and a shell layer (capsule layer) formed on the surface of the core. Moreover, you may make an external additive adhere to the surface of a shell layer as needed. In order to improve the toner fixing property in a wide temperature range, to improve the storage stability of the toner at a high temperature, or to improve the toner blocking resistance, a capsule toner and a method for producing the same are proposed. ing.

  For example, in the capsule toner manufacturing method described in Patent Document 1, mixed fine particles composed of release agent fine particles and resin particles are attached to the surface of the core. Subsequently, the core is caused to flow in an air stream while ethanol is sprayed onto the core to which the mixed fine particles are adhered. Thereby, a resin film is formed on the surface of the core.

JP 2011-81344 A

  However, in the toner described in Patent Document 1, it is difficult to uniformly cover the surface of the core with the resin film, and it is difficult to completely cover the core with the resin film. As a result, the core is easily exposed. For this reason, when the toner described in Patent Document 1 is stored at a high temperature, the release agent oozes out or the toner particles are easily aggregated due to the influence of heat or water vapor.

  In order to improve the chargeability of the toner, it may be considered to add a charge control agent to the shell layer. However, when a charge control agent is added to the shell layer, the adhesion between the fine particles constituting the shell layer decreases, and the interface of the particles tends to remain in the shell layer. For this reason, it becomes difficult to prevent the release agent from seeping out or aggregation of toner particles.

  The present invention has been made in view of the above problems, and an object thereof is to provide a toner having excellent chargeability and a method for producing the same. Another object of the present invention is to provide a toner excellent in both fixability and storage stability and a method for producing the same.

The toner manufacturing method according to the present invention includes a step of forming a core and a step of forming a shell layer on the surface of the core. In the step of forming the shell layer, the aqueous emulsion is sprayed in an air stream having a flow velocity of 30 m / second or more in which the core is dispersed. The aqueous emulsion includes resin particles containing a charge control agent in an amount of 0.3% by mass to 10.0% by mass with respect to the mass of the resin. The airflow circulates in an annular flow path. The aqueous emulsion contains a surfactant. The solid content concentration of the aqueous emulsion is 5% by mass or more and 50% by mass or less. The core contains a polyester resin as a binder resin. The resin contained in the resin particles is a styrene acrylic resin. The charge control agent contained in the resin particles is a nigrosine compound.

The toner according to the present invention includes a plurality of toner particles. The toner particles have a core and a shell layer formed on the surface of the core. The shell layer contains 0.3 mass% or more and 10.0 mass% or less of a charge control agent with respect to the mass of the resin and the resin. The core contains a polyester resin as a binder resin. The resin contained in the shell layer is a styrene acrylic resin. The charge control agent contained in the shell layer is a nigrosine compound.

  According to the present invention, it is possible to provide a toner having excellent chargeability and a method for producing the same. Further, according to the present invention, in addition to or instead of this effect, it is possible to provide a toner excellent in both fixability and storage stability and a method for producing the same. There is a case.

FIG. 3 is a diagram illustrating toner particles constituting the toner according to the exemplary embodiment of the present invention. It is a figure for demonstrating the method of reading a glass transition point from an endothermic curve. It is a figure for demonstrating the method of reading a softening point from a S-shaped curve. It is a figure which shows an example of the surface modification apparatus used for manufacture of the toner which concerns on embodiment of this invention. It is sectional drawing of the surface modification apparatus shown by FIG. It is a side view of the surface modification apparatus shown by FIG. 3 is an SEM photograph showing the surface of a core of toner particles contained in a toner according to an example of the present invention. 4 is an SEM photograph showing the surface of a shell layer of toner particles contained in a toner according to an example of the present invention. 4 is a TEM photograph of toner particles contained in a toner according to a comparative example. 4 is a TEM photograph of toner particles contained in a toner according to an example of the present invention.

Hereinafter, embodiments of the present invention will be described.
The toner according to this embodiment is a capsule toner for developing an electrostatic image. The toner of this embodiment is a powder composed of a large number of particles (hereinafter referred to as toner particles). The toner according to the exemplary embodiment can be used in, for example, an electrophotographic apparatus.

  In an electrophotographic apparatus, an electrostatic image is developed using a developer containing toner. As a result, charged toner adheres to the electrostatic latent image formed on the photoreceptor. After the adhered toner is transferred to the transfer belt, the toner image on the transfer belt is further transferred to a recording medium (for example, paper). Thereafter, the toner is heated and fixed on the recording medium. As a result, an image is formed on the recording medium. For example, a full color image can be obtained by superimposing toner images of four colors of black, yellow, magenta and cyan.

  Hereinafter, the configuration of the toner (particularly toner particles) according to the present embodiment will be described with reference to FIG. FIG. 1 is a view showing toner particles 10 constituting the toner according to the present embodiment.

  As shown in FIG. 1, the toner particle 10 includes a core 11, a shell layer 12 (capsule layer) formed on the surface of the core 11, and an external additive 13.

  The core 11 is composed of a binder resin 11a and an internal additive 11b (for example, a colorant, a release agent, and magnetic powder). The core 11 is covered with a shell layer 12. An external additive 13 is attached to the surface of the shell layer 12.

  However, the configuration of the toner particles is not limited to the above. For example, if not necessary, the internal additive 11b or the external additive 13 may be omitted. The toner particles may have a plurality of shell layers 12 on the surface of the core 11.

  Hereinafter, the core 11 (binder resin 11a and internal additive 11b), shell layer 12, and external additive 13 will be described in order.

[core]
The core 11 includes a binder resin 11a and an internal additive 11b (colorant, release agent, and magnetic powder). The core 11 does not contain a charge control agent. However, unnecessary components (coloring agent, release agent, magnetic powder, etc.) may be omitted depending on the use of the toner. Moreover, you may include a charge control agent in the core 11 as needed.

[Binder resin (core)]
Hereinafter, the binder resin 11a will be described.

  As the binder resin 11a, a thermoplastic resin is preferable.

  Preferred examples of the thermoplastic resin include styrene resin, acrylic resin, styrene acrylic resin, polyethylene resin, polypropylene resin, vinyl chloride resin, polyester resin, polyamide resin, polyurethane resin, and polyvinyl alcohol. Examples thereof include a resin, a vinyl ether resin, an N-vinyl resin, and a styrene-butadiene resin. Among them, the styrene acrylic resin and the polyester resin are excellent in the dispersibility of the colorant in the toner, the charging property of the toner, and the fixing property to the recording medium, respectively.

(Styrene acrylic resin)
Hereinafter, the styrene acrylic resin as the binder resin 11a will be described.

  The styrene acrylic resin is, for example, a copolymer of a styrene monomer and an acrylic monomer.

  Preferable examples of the styrenic monomer include styrene, α-methylstyrene, p-hydroxystyrene, m-hydroxystyrene, vinyltoluene, α-chlorostyrene, o-chlorostyrene, m-chlorostyrene, p-chloro. Styrene or p-ethylstyrene is mentioned.

  Preferable examples of the acrylic monomer include (meth) acrylic acid, particularly (meth) acrylic acid alkyl ester or (meth) acrylic acid hydroxyalkyl ester. Examples of the (meth) acrylic acid alkyl ester include methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, iso-propyl (meth) acrylate, and (meth) acrylic acid n-. Butyl, iso-butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, methyl (meth) methacrylate, ethyl (meth) methacrylate, n-butyl (meth) methacrylate, or (meth) Iso-butyl methacrylate is preferred. Examples of (meth) acrylic acid hydroxyalkyl esters include 2-hydroxyethyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, or 4- (meth) acrylic acid 4- Hydroxypropyl is preferred.

  When preparing a styrene acrylic resin, hydroxyl groups are introduced into the styrene acrylic resin by using a monomer having a hydroxyl group (p-hydroxystyrene, m-hydroxystyrene, or hydroxyalkyl (meth) acrylate). it can. For example, the hydroxyl value of the obtained styrene acrylic resin can be adjusted by appropriately adjusting the amount of the monomer having a hydroxyl group.

  When preparing the styrene acrylic resin, a carboxyl group can be introduced into the styrene acrylic resin by using (meth) acrylic acid as a monomer. For example, the acid value of the resulting styrene acrylic resin can be adjusted by appropriately adjusting the amount of (meth) acrylic acid used.

  In order to improve the strength or fixability of the core 11, the number average molecular weight (Mn) of the styrene acrylic resin as the binder resin 11 a is preferably 2000 or more and 3000 or less. The molecular weight distribution (the ratio Mw / Mn of the mass average molecular weight (Mw) to the number average molecular weight (Mn)) of the styrene acrylic resin is preferably 10 or more and 40 or less. Gel permeation chromatography can be used for the measurement of Mn and Mw of the binder resin 11a.

(Polyester resin)
Hereinafter, the polyester resin as the binder resin 11a will be described.

  The polyester resin can be obtained, for example, by polycondensation or copolycondensation of a divalent or trivalent or higher alcohol component and a divalent or trivalent or higher carboxylic acid component.

  Preferable examples of the divalent or trivalent or higher alcohol component of the polyester resin include diols, bisphenols, and trivalent or higher alcohols.

  Examples of diols include ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, 1,4-butanediol, neopentyl glycol, 1,4-butenediol, 1,5 -Pentanediol, 1,6-hexanediol, 1,4-cyclohexanedimethanol, dipropylene glycol, polyethylene glycol, polypropylene glycol or polytetramethylene glycol are preferred.

  As the bisphenols, for example, bisphenol A, hydrogenated bisphenol A, polyoxyethylenated bisphenol A, or polyoxypropylenated bisphenol A is preferable.

  Examples of the trivalent or higher alcohols include sorbitol, 1,2,3,6-hexanetetrol, 1,4-sorbitan, pentaerythritol, dipentaerythritol, tripentaerythritol, 1,2,4-butanetriol, 1,2,5-pentanetriol, glycerol, diglycerol, 2-methylpropanetriol, 2-methyl-1,2,4-butanetriol, trimethylolethane, trimethylolpropane, or 1,3,5-trihydroxy Methylbenzene is preferred.

  As the divalent or trivalent or higher carboxylic acid component of the polyester resin, for example, an ester-forming derivative (an acid halide, an acid anhydride, a lower alkyl ester, or the like) may be used. Here, “lower alkyl” means an alkyl group having 1 to 6 carbon atoms.

  Examples of the divalent carboxylic acid include maleic acid, fumaric acid, citraconic acid, itaconic acid, glutaconic acid, phthalic acid, isophthalic acid, terephthalic acid, cyclohexanedicarboxylic acid, succinic acid, adipic acid, sebacic acid, azelaic acid, malonic acid. Or alkyl or alkenyl succinic acid. Furthermore, examples of the alkenyl succinic acid include n-butyl succinic acid, n-butenyl succinic acid, isobutyl succinic acid, isobutenyl succinic acid, n-octyl succinic acid, n-octenyl succinic acid, n-dodecyl succinic acid, and n-dodecenyl succinic acid. , Isododecyl succinic acid, or isododecenyl succinic acid.

  Examples of the trivalent or higher carboxylic acid include 1,2,4-benzenetricarboxylic acid (trimellitic acid), 1,2,5-benzenetricarboxylic acid, 2,5,7-naphthalenetricarboxylic acid, 1,2,4. -Naphthalenetricarboxylic acid, 1,2,4-butanetricarboxylic acid, 1,2,5-hexanetricarboxylic acid, 1,3-dicarboxyl-2-methyl-2-methylenecarboxypropane, 1,2,4-cyclohexanetricarboxylic acid Acid, tetra (methylenecarboxyl) methane, 1,2,7,8-octanetetracarboxylic acid, pyromellitic acid, or empole trimer acid are preferred.

  When the polyester resin is produced, the acid value and hydroxyl group of the polyester resin are appropriately changed by appropriately changing the amount of the divalent or trivalent or higher alcohol component and the amount of the divalent or trivalent or higher carboxylic acid component. The price can be adjusted. Moreover, when the molecular weight of the polyester resin is increased, the acid value and hydroxyl value of the polyester resin tend to decrease.

  In order to improve the strength or fixability of the core 11, the number average molecular weight (Mn) of the polyester resin as the binder resin 11a is preferably 1200 or more and 2000 or less. The molecular weight distribution (the ratio Mw / Mn of the mass average molecular weight (Mw) to the number average molecular weight (Mn)) of the polyester resin is preferably 9 or more and 20 or less. Gel permeation chromatography can be used for the measurement of Mn and Mw of the binder resin 11a.

  Hereinafter, a method of reading Tg of the binder resin 11a from the endothermic curve will be described with reference to FIG. FIG. 2 is a graph showing an example of an endothermic curve.

  In measuring Tg, an endothermic curve is measured using a differential scanning calorimeter. For example, an endothermic curve as shown in FIG. 2 is obtained. The Tg of the binder resin 11a can be obtained from the change point of the specific heat in the endothermic curve of the binder resin 11a.

  Next, a method for reading the Tm of the binder resin 11a from the S-shaped curve will be described with reference to FIG. FIG. 3 is a graph showing an example of an S-shaped curve.

  The Tm of the binder resin 11a can be measured using an elevated flow tester. Specifically, the measurement sample is set on an elevated flow tester, and the sample is melted and flowed out under predetermined conditions. Thereby, an S-shaped curve (S-shaped curve related to temperature (° C.) / Stroke (mm)) is obtained. The Tm of the binder resin 11a can be read from the obtained S-shaped curve. In FIG. 3, S1 represents the maximum stroke value, and S2 represents the baseline stroke value on the low temperature side. The temperature at which the stroke value in the S-shaped curve is (S1 + S2) / 2 is defined as Tm of the measurement sample.

  The softening point (Tm) of the binder resin 11a is preferably 100 ° C. or less, and more preferably 95 ° C. or less. When the Tm of the binder resin 11a is 100 ° C. or lower (more preferably 95 ° C. or lower), sufficient fixability can be obtained even during high-speed fixing. In addition, Tm of the binder resin 11a can be adjusted by combining a plurality of binder resins having different Tm.

[Colorant (core)]
Hereinafter, the colorant contained in the core 11 (internal additive 11b) will be described.

  As the colorant, for example, a known pigment or dye can be used according to the color of the toner particles 10. The amount of the colorant to be used is preferably 1 part by mass or more and 20 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 11a.

(Black colorant)
The core 11 of the toner particles 10 according to the present embodiment may contain a black colorant. The black colorant is composed of, for example, carbon black. In addition, a colorant that is toned to black using a colorant such as a yellow colorant, a magenta colorant, and a cyan colorant can also be used.

(Coloring agent)
The core 11 of the toner particle 10 according to the present embodiment may contain a color colorant such as a yellow colorant, a magenta colorant, or a cyan colorant.

  The yellow colorant is preferably composed of, for example, a condensed azo compound, an isoindolinone compound, an anthraquinone compound, an azo metal complex, a methine compound, or an allylamide compound. Examples of yellow colorants include C.I. I. Pigment Yellow (3, 12, 13, 14, 15, 17, 62, 74, 83, 93, 94, 95, 97, 109, 110, 111, 120, 127, 128, 129, 147, 151, 154, 155 168, 174, 175, 176, 180, 181, 191 or 194), Neftol Yellow S, Hansa Yellow G, or C.I. I. Butt yellow is preferred.

  The magenta colorant is preferably composed of, for example, a condensed azo compound, diketopyrrolopyrrole compound, anthraquinone compound, quinacridone compound, basic dye lake compound, naphthol compound, benzimidazolone compound, thioindigo compound, or perylene compound. Examples of magenta colorants include C.I. I. Pigment Red (2, 3, 5, 6, 7, 19, 23, 48: 2, 48: 3, 48: 4, 57: 1, 81: 1, 122, 144, 146, 150, 166, 169, 177 184, 185, 202, 206, 220, 221 or 254).

  The cyan colorant is preferably composed of, for example, a copper phthalocyanine compound, a copper phthalocyanine derivative, an anthraquinone compound, or a basic dye lake compound. Examples of cyan colorants include C.I. I. Pigment blue (1, 7, 15, 15: 1, 15: 2, 15: 3, 15: 4, 60, 62, or 66), phthalocyanine blue, C.I. I. Bat Blue, or C.I. I. Acid blue is preferred.

[Release agent (core)]
Hereinafter, the mold release agent contained in the core 11 (internal additive 11b) will be described.

  The release agent is used for the purpose of improving the fixing property or offset resistance of the toner. In order to improve the fixing property or the offset resistance, the amount of the release agent used is preferably 1 part by mass or more and 30 parts by mass or less with respect to 100 parts by mass of the binder resin 11a. It is more preferable that the amount is not more than part by mass.

  In one example, the release agent may be composed of an aliphatic hydrocarbon wax such as low molecular weight polyethylene, low molecular weight polypropylene, polyolefin copolymer, polyolefin wax, microcrystalline wax, paraffin wax, or Fischer-Tropsch wax. preferable. In another example, the release agent is preferably composed of an oxide of an aliphatic hydrocarbon wax such as an oxidized polyethylene wax or a block copolymer of oxidized polyethylene wax. In another example, it is preferred that the release agent is composed of a vegetable wax such as candelilla wax, carnauba wax, wood wax, jojoba wax, or rice wax. In another example, the release agent is preferably composed of animal wax such as beeswax, lanolin, or spermaceti. In another example, the release agent is preferably composed of a mineral wax such as ozokerite, ceresin, or vetrolactam. In another example, it is preferable that the mold release agent is composed of waxes based on fatty acid esters such as montanic acid ester wax or caster wax. In another example, it is preferable that the release agent is composed of a wax obtained by deoxidizing a part or all of a fatty acid ester such as deoxidized carnauba wax.

[Magnetic powder (core)]
Hereinafter, the magnetic powder contained in the core 11 (internal additive 11b) will be described.

  When toner is used as a one-component developer, the amount of magnetic powder used is preferably 35 parts by weight or more and 60 parts by weight or less, and 40 parts by weight or more and 60 parts by weight or less with respect to 100 parts by weight of the total amount of toner. It is more preferable. When the toner is used as a two-component developer, the amount of magnetic powder used is preferably 20 parts by mass or less and more preferably 15 parts by mass or less with respect to 100 parts by mass of the total amount of toner.

  Magnetic powder is made ferromagnetized, for example, iron (ferrite or magnetite), ferromagnetic metal (cobalt or nickel), alloy containing iron and / or ferromagnetic metal, compound containing iron and / or ferromagnetic metal, heat treatment It is preferably composed of a processed ferromagnetic alloy or chromium dioxide.

  The particle size of the magnetic powder is preferably 0.1 μm or more and 1.0 μm or less, and more preferably 0.1 μm or more and 0.5 μm or less. When the particle diameter of the magnetic powder is in such a range, the magnetic powder can be easily dispersed uniformly in the binder resin 11a.

[Shell layer]
As a suitable example of resin which comprises the shell layer 12, an acrylic resin or a styrene acrylic resin is mentioned.

  As a method for forming the shell layer 12, a method in which resin fine particles are attached to the surface of the core 11 and then the resin fine particles are united is preferable.

  In order to make the particle diameter of the resin fine particles uniform, it is preferable to form the resin fine particles using a resin obtained by addition polymerization of a monomer having an unsaturated bond.

  Suitable examples of the monomer having an unsaturated bond include styrene, α-methylstyrene, vinyl toluene, α-chlorostyrene, o-chlorostyrene, m-chlorostyrene, p-chlorostyrene, p-ethylstyrene, or divinyl. Vinyl aromatic compounds such as benzene; methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, cyclohexyl (meth) acrylate, (meth) acrylic (Meth) acrylic acid derivatives such as phenyl acid, ethyl β-hydroxyacrylate, ethyl β-hydroxymethacrylate, propyl γ-hydroxyacrylate, butyl δ-hydroxyacrylate, ethylene glycol dimethacrylate, or diethylene glycol dimethacrylate; Vinyl formate Vinyl esters such as vinyl acetate or vinyl propionate; vinyl ethers such as vinyl methyl ether, vinyl ethyl ether, vinyl-n-butyl ether, vinyl phenyl ether, or vinyl cyclohexyl ether; ethylene, propylene, isobutylene butene-1, pentene Examples include olefins such as -1,4-methylpentene-1, butadiene, isoprene, or chloroprene.

  Examples of the addition polymerization method for the monomer having an unsaturated bond include methods such as solution polymerization, bulk polymerization, emulsion polymerization, and suspension polymerization. In order to make the particle diameter of the resin fine particles uniform, an emulsion polymerization method is particularly preferable.

  Examples of the polymerization initiator that can be used for addition polymerization of a monomer having an unsaturated bond include potassium persulfate, acetyl peroxide, decanoyl peroxide, lauroyl peroxide, benzoyl peroxide, azobisisobutyronitrile, 2, 2 Examples include '-azobis-2,4-dimethylvaleronitrile or 2,2'-azobis-4-methoxy-2,4-dimethylvaleronitrile. The amount of these polymerization initiators used is preferably 0.1% by mass or more and 15% by mass or less based on the total amount of monomers.

  When producing resin fine particles by an emulsion polymerization method, the reaction solution may be emulsified using a surfactant. In emulsion polymerization, at least one selected from a cationic surfactant, an anionic surfactant, and a nonionic surfactant can be used.

  Specific examples of the cationic surfactant include dodecyl ammonium chloride, dodecyl ammonium bromide, dodecyl trimethyl ammonium bromide, dodecyl pyridinium chloride, dodecyl pyridinium bromide, or hexadecyl trimethyl ammonium bromide.

  Specific examples of the anionic surfactant include fatty acid soaps such as sodium stearate and sodium dodecanoate, and sulfonates such as sodium dodecyl sulfate and sodium dodecylbenzene sulfonate.

  Specific examples of the nonionic surfactant include polyoxyethylene dodecyl ether, polyoxyethylene hexadecyl ether, polyoxyethylene nonyl phenyl ether, polyoxyethylene sorbitan monooleate ether, or monodecanoyl sucrose.

  The average particle diameter of the resin fine particles is preferably 50 nm or more and 300 nm or less, and more preferably 100 nm or more and 150 nm or less. When resin fine particles having an average particle diameter of 50 nm or more and 300 nm or less are used, the shell layer 12 having a desired structure is easily formed on the surface of the core 11. The average particle diameter of the resin fine particles can be adjusted by changing the polymerization conditions. Moreover, the average particle diameter of the resin fine particles can be adjusted by pulverization or classification. The average particle diameter of the resin fine particles can be measured as a volume average diameter using a laser diffraction / scattering particle size distribution measuring apparatus.

  The glass transition point of the resin constituting the resin fine particles is preferably 56 ° C. or higher, and more preferably 58 ° C. or higher and 62 ° C. or lower.

  The resin constituting the resin fine particles preferably has a mass average molecular weight (Mw) of 5000 or more and 20000 or less. The mass average molecular weight (Mw) of the resin can be measured by gel permeation chromatography.

[Charge control agent (shell layer)]
Hereinafter, the charge control agent constituting the shell layer 12 will be described.

  In order to improve charge rise characteristics, durability, stability, cost merit, etc., the amount of the positively chargeable charge control agent used is 0.3 mass relative to 100 mass parts of the resin forming the shell layer 12. Part to 10.0 parts by weight, more preferably 0.5 parts to 5.0 parts by weight.

  The positively chargeable charge control agent is preferably composed of, for example, an azine compound, a nigrosine compound, a metal salt of naphthenic acid (or higher fatty acid), an alkoxylated amine, an alkylamide, or a quaternary ammonium salt. Among these, a nigrosine compound is particularly preferable in that quick charge rising property can be obtained. These can be used alone or in combination of two or more.

  Examples of the azine compounds include pyridazine, pyrimidine, pyrazine, orthooxazine, metaoxazine, paraoxazine, orthothiazine, metathiazine, parathiazine, 1,2,3-triazine, 1,2,4-triazine, 1,3,5-triazine. 1,2,4-oxadiazine, 1,3,4-oxadiazine, 1,2,6-oxadiazine, 1,3,4-thiadiazine, 1,3,5-thiadiazine, 1,2,3,4-tetrazine 1,2,4,5-tetrazine, 1,2,3,5-tetrazine, 1,2,4,6-oxatriazine, 1,3,4,5-oxatriazine, phthalazine, quinazoline, or quinoxaline preferable. Examples of the direct dye made of the azine compound include azine fast red FC, azine fast red 12BK, azine violet BO, azine brown 3G, azine light brown GR, azine dark green BH / C, azine deep black EW, and azine. Deep black 3RL is preferred. As the nigrosine compound, for example, nigrosine, nigrosine salt, or nigrosine derivative is preferable. As the acid dye made of a nigrosine compound, for example, nigrosine BK, nigrosine NB, or nigrosine Z is preferable. As the quaternary ammonium salt, for example, benzylmethylhexyldecylammonium or decyltrimethylammonium chloride is preferable.

  The positively chargeable charge control agent may be composed of a resin having a quaternary ammonium salt, carboxylate, or carboxyl group as a functional group. The positively chargeable charge control agent may be composed of, for example, a styrene resin, an acrylic resin, a styrene-acrylic resin, or a polyester resin having any of a quaternary ammonium salt, a carboxylate, and a carboxyl group. . These resins may be oligomers or polymers.

[External additive]
Hereinafter, the external additive 13 will be described. Hereinafter, the particles before being treated with the external additive 13 are referred to as “toner mother particles”.

  The external additive 13 is used to improve the fluidity or handleability of the toner particles 10 and adheres to the surface of the shell layer 12. In order to improve fluidity or handleability, the amount of the external additive 13 used is preferably 0.5 parts by mass or more and 10 parts by mass or less with respect to 100 parts by mass of the toner base particles. More preferably, it is 5 parts by mass or less.

  The external additive 13 is preferably composed of, for example, silica or a metal oxide (for example, alumina, titanium oxide, magnesium oxide, zinc oxide, strontium titanate, or barium titanate).

  In order to improve fluidity or handleability, the particle diameter of the external additive 13 is preferably 0.01 μm or more and 1.0 μm or less.

[Two-component developer]
The toner of this embodiment may be mixed with a carrier to produce a two-component developer.

  When preparing a two-component developer, it is preferable to use a magnetic carrier as a carrier. An example of a suitable carrier is a carrier in which a carrier core material is coated with a resin. Examples of carrier cores include particles of metals such as iron, oxidized iron, reduced iron, magnetite, copper, silicon steel, ferrite, nickel, or cobalt, or these materials such as manganese, zinc, or aluminum. Particles of alloys with various metals; particles of iron alloys such as iron-nickel alloys or iron-cobalt alloys; titanium oxide, aluminum oxide, copper oxide, magnesium oxide, lead oxide, zirconium oxide, silicon carbide, magnesium titanate, Ceramic particles such as barium titanate, lithium titanate, lead titanate, lead zirconate, or lithium niobate; high dielectric constant materials such as ammonium dihydrogen phosphate, potassium dihydrogen phosphate, or Rochelle salt Particle: Examples thereof include a resin carrier in which the above magnetic particles are dispersed in a resin.

  Examples of the resin for coating the carrier core material include (meth) acrylic polymer, styrene polymer, styrene- (meth) acrylic copolymer, olefin polymer (polyethylene, chlorinated polyethylene, or polypropylene). , Polyvinyl chloride, polyvinyl acetate, polycarbonate, cellulose resin, polyester resin, unsaturated polyester resin, polyamide resin, polyurethane resin, epoxy resin, silicone resin, fluororesin (polytetrafluoroethylene, polychlorotrifluoroethylene, or polyfluoride) Vinylidene chloride), phenol resin, xylene resin, diallyl phthalate resin, polyacetal resin, or amino resin. These resins can be used in combination of two or more.

The particle diameter of the carrier is a particle diameter measured using an electron microscope, and is preferably 20 μm or more and 200 μm or less, and more preferably 30 μm or more and 150 μm or less. The apparent density of the carrier is preferably 2400 kg / m ³ or more and 3000 kg / m ³ or less.

  The toner content is preferably 1% by mass or more and 20% by mass or less, and more preferably 3% by mass or more and 15% by mass or less with respect to the mass of the two-component developer. When the toner content is 1% by mass or more and 20% by mass or less with respect to the mass of the two-component developer, it becomes easy to form an image with a high image density using the toner. In addition, toner charging defects are less likely to occur. As a result, contamination inside the image forming apparatus can be suppressed.

  In the toner according to the exemplary embodiment, the shell layer 12 contains 0.3% by mass or more and 10.0% by mass or less of a charge control agent. Therefore, a toner having excellent chargeability (charge amount) can be obtained without using a charge control agent in forming the core 11.

  In order to improve both the fixability and the storage stability, the average thickness of the shell layer 12 is preferably 30 nm or more and 300 nm or less.

  In order to suppress exudation of a release agent or aggregation of toner particles, among the plurality of toner particles 10 contained in the toner, the shell layer 12 of the toner particles 10 having a diameter of 6 μm to 8 μm is formed on the surface of the core 11. It is preferable not to have cracks in a direction substantially perpendicular to the direction.

  In order to suppress seepage of the release agent or aggregation of the toner particles, among the plurality of toner particles 10 contained in the toner, the surface of the shell layer 12 of the toner particles 10 having a diameter of 6 μm to 8 μm is particulate. It is preferred that no charge control agent is present. For example, when the amount of the charge control agent added is large, coalescence of the particles of the charge control agent is incomplete, and the particulate charge control agent tends to be exposed on the surface of the shell layer 12.

  In order to suppress exudation of the release agent or aggregation of the toner particles, among the plurality of toner particles 10 included in the toner, the toner particles 10 having a diameter of 6 μm or more and 8 μm or less are formed between the core 11 and the shell layer 12. It is preferable to have an interface between them.

  Next, a toner manufacturing method according to this embodiment will be described.

  The toner manufacturing method according to the present embodiment includes a step of forming the core 11 and a step of forming the shell layer 12 on the surface of the core 11. In the step of forming the shell layer 12, the aqueous emulsion is sprayed into an air flow in which the core 11 is dispersed and having a flow velocity of 30 m / second or more. The aqueous emulsion to be sprayed contains resin particles containing a charge control agent in an amount of 0.3% by mass or more and 10.0% by mass or less.

  Hereinafter, the step of forming the core 11 and the step of forming the shell layer 12 will be described in order.

[Step of forming core]
In an example of a method for forming a core, first, a binder resin, a colorant, a release agent, and magnetic powder are mixed. Subsequently, the obtained mixture is melt-kneaded. Subsequently, the obtained melt-kneaded product is pulverized and classified.

[Step of forming shell layer]
Hereinafter, the step of forming the shell layer will be described mainly with reference to FIGS.

(Surface modification device)
Hereinafter, the surface modification apparatus used in the step of forming the shell layer 12 will be described. As an example of the surface modification apparatus, there is “Hybridization system (NHS)” manufactured by Nara Machinery Co., Ltd.

  FIG. 4 is a diagram illustrating an example of the surface modifying apparatus (surface modifying apparatus 100). 5 is a cross-sectional view taken along line VV in FIG. FIG. 6 is a side view of the surface modifying apparatus shown in FIG.

  The surface modification device 100 is used in the step of forming the shell layer 12. As shown in FIGS. 4 to 6, the surface modification apparatus 100 includes a powder flow path 101, a stirring chamber 102, a spray unit 103, a powder input unit 104, and a powder recovery unit 105.

  The powder channel 101 is composed of a tube bent in a C shape (see FIG. 5). The cross section of the tube is, for example, circular.

  One end (end portion 101 a) of the powder passage 101 and the other end (end portion 101 b) of the powder passage 101 are communicated with each other via the stirring chamber 102. An annular channel is formed by communicating the powder channel 101 and the stirring chamber 102 (see FIG. 5). In the stirring chamber 102, a stirring device 110 is provided (see FIG. 5). The stirring device 110 has a blade 110a. By using a motor as a power source of the stirring device 110, the blades 110a of the stirring device 110 can be rotated. When the blade 110a of the stirring device 110 rotates, the gas in the flow path is stirred. The stirrer 110 pushes gas toward the end 101a of the powder channel 101. As a result, an air flow is formed from one end (end portion 101a) of the powder passage 101 to the other end (end portion 101b) of the powder passage 101 through the powder passage 101 (in FIG. 5). (See arrow F).

  The powder flow path 101 and the stirring chamber 102 are provided with a temperature adjusting jacket (not shown). By flowing a cooling medium or a heating medium into the inner space of the jacket, the powder channel 101 and the stirring chamber 102 can be heated or cooled. The temperature adjusting jacket is preferably provided in the entire powder flow path 101 and the stirring chamber 102.

  The spray unit 103 sprays a liquid (aqueous emulsion in this embodiment) into the powder channel 101. The spray unit 103 includes a spray liquid supply unit, a carrier gas supply unit, and a two-fluid nozzle. The spray liquid supply unit supplies the aqueous emulsion to the two-fluid nozzle. The carrier gas supply unit supplies a carrier gas (for example, compressed air) to the two-fluid nozzle. The two-fluid nozzle sprays a mixture of an aqueous emulsion and a carrier gas into the powder channel 101.

  The powder input unit 104 includes an input port 104a and an electromagnetic valve 104b. The core 11 is supplied to a charging port 104a from a hopper (not shown). And the core 11 can be supplied in the powder flow path 101 by opening the electromagnetic valve 104b. Further, the supply of the core 11 can be stopped by closing the electromagnetic valve 104b.

  The powder recovery unit 105 includes a recovery tank 105a and an electromagnetic valve 105b. By opening the electromagnetic valve 105b, the toner (toner mother particles) in the flow path can be collected in the collection tank 105a. Further, the toner collection can be stopped by closing the electromagnetic valve 105b.

(Aqueous emulsion)
The aqueous emulsion sprayed by the spray unit 103 includes resin particles. This resin particle contains 0.3 mass% or more and 10.0 mass% or less of charge control agents with respect to the mass of resin in particle | grains. The resin particles contained in the sprayed aqueous emulsion are dispersed while flowing together with the core 11 in the annular flow path (powder flow path 101 and stirring chamber 102).

  The aqueous emulsion preferably contains a surfactant. Thereby, it is considered that the resin particle layer (shell layer 12) is easily formed uniformly on the surface of the core 11.

  The average particle size of the resin particles in the aqueous emulsion is preferably 50 nm or more and 300 nm or less, and more preferably 100 nm or more and 150 nm or less.

  The solid content concentration of the resin particles in the aqueous emulsion is preferably 5% by mass or more and 50% by mass or less, and more preferably 10% by mass or more and 20% by mass or less. When the shell layer 12 is formed using such an aqueous emulsion, the surface of the core 11 can easily be uniformly covered with the resin particle layer (shell layer 12). As a result, it becomes easy to form the shell layer 12 having a desired shape.

  An example of the aqueous medium contained in the aqueous emulsion is water. The aqueous emulsion may contain a water-soluble organic solvent in addition to water. The content of the water-soluble organic solvent is preferably 20% by mass or less, more preferably 10% by mass or less, and still more preferably 5% by mass or less with respect to the mass of the aqueous medium.

  Hereinafter, an example of a method for preparing an aqueous emulsion of resin particles will be described.

  A coarsely pulverized resin composition containing a charge control agent of 0.3% by mass or more and 10.0% by mass or less with respect to the mass of the resin and a dispersant (surfactant) are added to the aqueous medium. Thereby, a dispersion of resin particles is prepared.

  Subsequently, the resin particle dispersion is heated to a temperature higher by 10 ° C. or more than the softening point of the resin (resin particles). The softening point of the resin can be measured using, for example, a flow tester.

  Subsequently, a strong shearing force is applied to the heated dispersion of resin particles using a high-speed stirring device (for example, “NV200” manufactured by Yoshida Kikai Kogyo Co., Ltd.) equipped with a temperature controller. Thereby, an aqueous emulsion of resin particles is prepared.

(Core distribution)
In the step of forming the shell layer 12, an air flow having a flow velocity of 30 m / second or more is generated in the annular flow path (the powder flow path 101 and the stirring chamber 102) using the stirring device 110. Then, the core 11 is dispersed in the airflow. Thereby, the core 11 flows in the airflow. The direction in which the core 11 flows in the annular channel (powder channel 101 and stirring chamber 102) is substantially constant. Further, since the air current circulates through the annular flow path, the core 11 easily collides with the inner wall of the flow path. When the core 11 collides with the inner wall of the flow path, the formation of the shell layer 12 is promoted.

(Water-based emulsion spraying)
After the core 11 is dispersed in an air flow having a flow velocity of 30 m / sec or more, the aqueous emulsion is sprayed into the air flow using the spray unit 103. At this time, since the core 11 is flowing in the airflow, the resin particles contained in the aqueous emulsion are likely to adhere to the surface of the core 11 without aggregating. As a result, the entire surface of the core 11 is easily covered with the resin particles.

  When spraying the aqueous emulsion, the temperature in the powder channel 101 is preferably 15 ° C. or higher. Moreover, aggregation of the core 11 can be suppressed by setting the temperature in the powder channel 101 to be equal to or lower than the glass transition temperature (Tg) of the core 11. As the core 11 flows through the powder channel 101, the temperature in the powder channel 101 becomes substantially uniform.

  When spraying the aqueous emulsion, the temperature of the aqueous emulsion is preferably 30 ° C. or higher and 100 ° C. or lower, and more preferably 40 ° C. or higher and 80 ° C. or lower. When the temperature of the aqueous emulsion is 30 ° C. or higher and 100 ° C. or lower, the formation of the shell layer 12 is promoted.

  When the aqueous emulsion is sprayed onto the core 11, resin particles adhere to the core 11. At this time, the liquid contained in the aqueous emulsion moves to the outside of the toner through minute gaps between the resin particles (so-called capillary phenomenon). At this time, a cohesive force is generated between the resin particles. Moreover, since the core 11 is moving at high speed in the air flow, it collides with the inner wall of the powder flow path 101 and receives a large external force. The coalescence of the resin particles is promoted by the cohesive force and the external force. When the resin particles are united, the resin particles attached to the surface of the core 11 are deformed, and the interface between the resin particles disappears. The unitized resin particles constitute the shell layer 12.

  The step of forming the shell layer 12 may be performed in a state where a dried gas (for example, dry air or dry nitrogen) is introduced into the flow path of the surface modification device 100. When the shell layer 12 is formed in such a state, it becomes easy to omit or simplify a toner mother particle drying step described later.

[Dry]
Through the above-described steps of forming the core 11 and the above-described steps of forming the shell layer 12, toner base particles are manufactured. Thereafter, if necessary, the aqueous medium attached to the toner base particles is evaporated. Specifically, the toner base particles are dried using a dryer. Examples of dryers include fluidized bed dryers, kiln dryers, or tumbler dryers. When the toner base particles are dried under reduced pressure, evaporation of the aqueous medium is easily promoted. The drying temperature is preferably 30 ° C. or higher and 100 ° C. or lower, and more preferably 40 ° C. or higher and 80 ° C. or lower.

  In the toner manufacturing method according to the present embodiment, in the process of forming the shell layer 12, the aqueous medium in the aqueous emulsion is often removed from the toner base particles in many cases. For this reason, the drying process of the toner base particles can often be omitted or simplified.

[External attachment]
The toner particles 10 are manufactured by attaching (externally adding) the external additive 13 to the surface of the toner base particles. Hereinafter, the external addition method according to the present embodiment will be described.

  As a suitable example of the external addition method, the toner base particles and the external additive 13 are mixed with a toner mixer or a mixer such as a Nauter mixer under the condition that the external additive 13 is not embedded in the toner base particles. The method of mixing is mentioned.

[Method for producing two-component developer]
A preferred example of a method for producing a two-component developer is a method in which a toner and a carrier are mixed using a mixing device such as a ball mill.

  In the toner manufacturing method according to the present embodiment described above, an aqueous emulsion containing resin particles is sprayed in the step of forming the shell layer 12. The resin particles contained in the aqueous emulsion contain 0.3% by mass or more and 10.0% by mass or less of a charge control agent with respect to the mass of the resin. When the resin particles of the aqueous emulsion contain an appropriate amount of the charge control agent, it is possible to produce a toner having excellent chargeability.

  In the toner manufacturing method according to the present embodiment, when the shell layer 12 is formed, the aqueous emulsion is sprayed in an air current having a flow velocity of 30 m / second or more in which the core 11 is dispersed. For this reason, the shell layer 12 is easily formed uniformly on the surface of the core 11. Further, the surface of the core 11 is easily covered with the shell layer 12. By completely covering the core 11 with the shell layer 12, it is possible to suppress seepage of the release agent or aggregation of toner particles. As a result, it is possible to produce a toner excellent in both fixability and storage stability.

  Examples of the present invention will be described below.

  In this example, toners A to H (see Table 1 to be described later) prepared under predetermined conditions were evaluated. Hereinafter, a method for preparing the toners A to H will be described.

[Method for Preparing Toner A]
Hereinafter, a method for preparing the toner A will be described.

<Step of forming the core>
80% by mass of polyester resin (binder resin 11a), 15% by mass of colorant, and 5% by mass of release agent are added to a Henschel mixer (“FM20B” manufactured by Nihon Coke Industries Co., Ltd.) based on the total mass of all raw materials. And mixing for 3 minutes at 2500 rpm.

  A polyester resin manufactured by Kao Corporation was used as the binder resin 11a. This polyester resin had a glass transition point (Tg) of 58 ° C., a melting point of 110 ° C., and a mass average molecular weight (Mw) of 45000.

  As the colorant, Pigment Blue (“P.B15-3” manufactured by Sanyo Pigment Co., Ltd.) was used. As the mold release agent, ester wax (“WEP-3” manufactured by NOF Corporation) was used.

  In the formation of the core 11, no charge control agent was used.

  Subsequently, the mixture was melt kneaded using a twin screw extruder ("PCM-30" manufactured by Ikegai Co., Ltd.) under the conditions of a rotation speed of 300 rpm, a cylinder temperature of 110 ° C, and an input amount of 6 kg / hour. Subsequently, using a drum flaker manufactured by Nippon Coke Kogyo Co., Ltd., the melt-kneaded product was spread so that the plate thickness was about 2 mm, and then cooled and solidified.

  Subsequently, the plate of the kneaded material was coarsely pulverized using a pulverizer having a screen opening of 2 mm ("Rohtoplex" manufactured by Alpine). Subsequently, the coarsely pulverized product was finely pulverized using a pulverizer (“Turbo Mill T250” manufactured by Freund Turbo Inc.).

  Subsequently, the finely pulverized product was classified using an elbow jet classifier (“EJ-L-3” manufactured by Nippon Steel Mining Co., Ltd.). As a result, a core 11 having a median diameter (volume distribution standard) of 7.0 μm was obtained. A particle size distribution measuring device (“Multisizer 3” manufactured by Beckman Coulter, Inc.) was used to measure the particle diameter (median diameter) of the core 11.

<Step of forming a shell layer>
For the formation of the shell layer 12, a “hybridization system (NHS-1 type)” manufactured by Nara Machinery Co., Ltd. having a structure as shown in FIGS. 4 to 6 was used. Hereinafter, the step of forming the shell layer 12 will be described mainly with reference to FIGS. 1 and 4 to 6.

(Preparation of aqueous emulsion)
After heating to 150 ° C. to melt the resin in the container, 0.2% by mass of a charge control agent was added to the container with respect to the mass of the resin. Subsequently, the contents of the container were sufficiently stirred and then cooled. Thereby, a resin composition containing a charge control agent was obtained.

  As the resin, styrene acrylic resin was used. This styrene acrylic resin had a glass transition point (Tg) of 62 ° C., a melting point of 118 ° C., and a mass average molecular weight (Mw) of 16000.

  As the charge control agent, a nigrosine compound (“N-01” manufactured by Orient Chemical Co., Ltd.) was used.

  Subsequently, the resin composition was roughly pulverized using a pulverizer (“Turbomill T250” manufactured by Freund Turbo, Inc.) until the median diameter (volume distribution standard) was about 400 μm.

  Subsequently, 150 g of the coarsely pulverized resin composition, 15 g of sodium lauryl sulfate, and 835 g of ion-exchanged water were charged into a high-speed stirring device equipped with a temperature controller (“NV200” manufactured by Yoshida Kikai Kogyo Co., Ltd.). The treatment was performed three times under the conditions of 170 ° C. and a treatment pressure of 150 MPa. Thereby, an aqueous emulsion of resin particles was obtained. Thereafter, the solid content concentration of the aqueous emulsion was adjusted to 15% by mass. The median diameter (volume distribution standard) of the resin particles contained in the aqueous emulsion was 100 nm.

(Core distribution)
In the surface modification apparatus 100 (“Hybridization system (NHS-1 type)” manufactured by Nara Machinery Co., Ltd.), a jacket provided in the annular flow path (powder flow path 101 and stirring chamber 102) is used. The temperature in the path was adjusted to 20 ° C. Then, an air flow having a flow rate of 30 m / second or more was generated in the flow path using the stirring device 110. Subsequently, 200 g of the core 11 formed by the above-described procedure was dispersed in the air stream. While stirring at 8000 rpm using the stirring device 110, the core 11 was retained in the flow path for 10 minutes.

  Subsequently, the resin particle aqueous emulsion prepared in the above-described procedure is set in the spray unit 103, and the powder flow channel 101 is fed from the two-fluid nozzle of the spray unit 103 over a period of 45 minutes at a supply rate of 1.5 g / min. The aqueous emulsion was sprayed on. The total supply amount of the aqueous emulsion of resin particles was 70 g, of which the total supply amount of solids was 10.5 g.

  For 10 minutes after the completion of spraying, an air flow with a flow rate of 30 m / second or more was maintained. Thereby, the shell layer 12 was formed on the surface of the core 11. As a result, toner mother particles were formed. Thereafter, toner base particles were recovered from the powder recovery unit 105.

  The average thickness of the shell layer 12 of the obtained toner base particles was 200 nm or more and 250 nm or less. The average thickness of the shell layer 12 was measured by the following method.

  The toner base particles were dispersed in a room temperature curable epoxy resin and cured in an atmosphere at 40 ° C. for 2 days to obtain a cured product. The cured product was dyed with osmium tetroxide and then cut out using a microtome (“EM UC6” manufactured by Leica) equipped with a diamond knife to obtain a thin sample having a thickness of 200 nm. And the cross section of this sample was image | photographed using the transmission electron microscope (TEM) (The JEOL Co., Ltd. product "JSM-6700F").

  The thickness of the shell layer 12 was measured by analyzing the TEM image using image analysis software (“WinROOF” manufactured by Mitani Corporation). Specifically, two straight lines orthogonal to each other at the approximate center of the cross section of the toner base particles were drawn, and the lengths of four locations on the two straight lines intersecting the shell layer 12 were measured. Then, the average value of the measured lengths of the four locations was used as the thickness of the shell layer 12 of one toner base particle as a measurement target. The thickness of the shell layer 12 was measured for 10 or more toner mother particles contained in the toner, and the average of the 10 or more obtained measurement values was used as the evaluation value.

<External Addition>
100 parts by mass of toner base particle powder and 1 part by mass of powder of external additive (“silica RA200” manufactured by Nippon Aerosil Co., Ltd.) are charged into a Henschel mixer (“10C” manufactured by Nippon Coke Industries, Ltd.) and rotated. The contents of the mixing apparatus were stirred for 2 minutes under the conditions of several 3,000 rpm and jacket temperature of 20 ° C. As a result, a toner having a large number of toner particles 10 was obtained.

[Method for Preparing Toner B]
The preparation method of the toner B is almost the same as the preparation method of the toner A except that the content of the charge control agent in the shell layer 12 is changed from 0.2% by mass to 0.3% by mass.

[Method for Preparing Toner C]
The preparation method of the toner C is almost the same as the preparation method of the toner A except that the content of the charge control agent in the shell layer 12 is changed from 0.2% by mass to 0.5% by mass.

[Method for Preparing Toner D]
The preparation method of the toner D is substantially the same as the preparation method of the toner A except that the content of the charge control agent in the shell layer 12 is changed from 0.2% by mass to 1.0% by mass.

[Method for Preparing Toner E]
The preparation method of the toner E is almost the same as the preparation method of the toner A except that the content of the charge control agent in the shell layer 12 is changed from 0.2% by mass to 3.0% by mass.

[Method for Preparing Toner F]
The preparation method of the toner F is substantially the same as the preparation method of the toner A except that the content of the charge control agent in the shell layer 12 is changed from 0.2% by mass to 5.0% by mass.

[Method for Preparing Toner G]
The preparation method of the toner G is almost the same as the preparation method of the toner A except that the content of the charge control agent in the shell layer 12 is changed from 0.2% by mass to 10.0% by mass.

[Method for Preparing Toner H]
The preparation method of the toner H is almost the same as the preparation method of the toner A except that the content of the charge control agent in the shell layer 12 is changed from 0.2% by mass to 11.0% by mass.

[Evaluation method]
The evaluation method is as follows.

  The evaluation method of each sample (toners A to H) is as follows.

(Degree of aggregation)
3 g of a sample (toner) was placed in a 20 cc plastic bottle and allowed to stand for 12 hours in an environment of a temperature of 58 ° C. and a humidity of 50% RH. Subsequently, using a powder tester manufactured by Hosokawa Micron Co., Ltd., the toner was sieved under the conditions of a rheostat scale of 3.5 and a time of 30 seconds according to the manual. For sieving, a 140 mesh (mesh size 105 μm) sieve was used. Then, the degree of aggregation was calculated based on the following formula.
Aggregation degree (mass%) = 100 × mass of toner remaining on sieve after sieving / mass of toner before sieving

  When the degree of aggregation was 15% by mass or less, it was evaluated as “good”, and when the degree of aggregation was larger than 15% by mass, it was evaluated as “poor” (not good).

(Charge amount)
A sample (toner) 0.8 g and a FS-C5200DN carrier 10 g manufactured by Kyocera Document Solutions Co., Ltd. are put in a 20 cc plastic bottle and stirred for 30 minutes using a turbula mixer set to the maximum rotation speed. A two-component developer was prepared.

  For the measurement of the charge amount, a QM meter (“MODEL 210HS” manufactured by TREK) was used. Specifically, the toner in 0.10 g (± 0.01 g) of developer is sucked using the suction part of the QM meter, and the charge amount of the toner is calculated based on the amount of sucked toner and the display on the QM meter. did.

  When the charge amount was 10 μC / g or more and less than 45 μC / g, it was evaluated as “good”. When the charge amount was 45 μC / g or more, an image density defect due to charge-up was likely to occur, and therefore, it was evaluated as Δ (somewhat inferior). When the charge amount was less than 10 μC / g, fogging was likely to occur in the image, and therefore, it was evaluated as x (not good).

(Offset resistance)
A sample (toner) is set in a printer (modified machine of “FS-C5250” manufactured by Kyocera Document Solutions Co., Ltd.), a solid image of 30 mm × 30 mm is formed on the edge of the recording paper, and the minimum fixable temperature (cold offset) Non-occurrence temperature) and maximum fixable temperature (hot offset non-occurrence temperature) were measured. The presence or absence of occurrence of offset was confirmed visually.

  When the minimum fixable temperature was 165 ° C. or lower, it was evaluated as “good”, and when the minimum fixable temperature was higher than 165 ° C., it was evaluated as “poor” (not good).

  When the maximum fixable temperature was 190 ° C. or higher, it was evaluated as “good”, and when the maximum fixable temperature was lower than 190 ° C., it was evaluated as “poor” (not good).

(Image density, fogging)
A sample (toner) is set in a printer (a modified model of “FS-C5250” manufactured by Kyocera Document Solutions Co., Ltd.), a solid image of 30 mm × 30 mm is formed on the edge of the recording paper, and the image density (ID) ) And fog (FD) of the non-image area. A spectrophotometer (“Spectro Eye” manufactured by Sakata Inx Engineering Co., Ltd.) was used for measurement of image density (ID) and fog (FD).

  When the image density (ID) was 1.25 or more, it was evaluated as ◯ (good), and when the image density (ID) was less than 1.25, it was evaluated as x (not good).

  When the fog (FD) was 0.010 or less, it was evaluated as ◯ (good), and when the fog (FD) exceeded 0.010, it was evaluated as x (not good).

(crack)
Using a scanning electron microscope (SEM) (“JSM-6700 F” manufactured by JEOL Ltd.), the surface of each sample (toners A to H) was observed at a magnification of 10,000 times to evaluate the presence or absence of cracks. Specifically, the presence or absence of cracks was evaluated based on the SEM photograph of the photographed toner.

  Using a transmission electron microscope (TEM) (“JSM-6700 F” manufactured by JEOL Ltd.), the cross section of each sample (toners A to H) was observed at a magnification of 50000 to evaluate the presence or absence of cracks. Specifically, the presence or absence of cracks was evaluated based on a TEM photograph of the photographed toner. In this observation and photographing, a thin sample was prepared in the same manner as the method for measuring the thickness of the shell layer 12 described above, and a cross section of the sample was photographed using a TEM.

[Evaluation results]
Table 1 summarizes the evaluation results of toners A to H.

  In each of toners B to G, the charge amount was 10 μC / g or more and less than 45 μC / g. In toner A, the charge amount was less than 10 μC / g. With toner H, the charge amount was 45 μC / g or more.

  In each of toners A to G, the degree of aggregation was 15% by mass or less. With toner H, the degree of aggregation was greater than 15% by mass.

  In any of the toners A to H, the maximum fixable temperature was 190 ° C. or higher.

  In each of toners A to G, the minimum fixable temperature was 165 ° C. or lower. With toner H, the minimum fixable temperature was higher than 165 ° C.

  In each of toners A to G, the image density (ID) was 1.25 or more. For toner H, the image density (ID) was lower than 1.25.

  In each of the toners B to H, the fog (FD) was 0.010 or less. With toner A, the fog (FD) was higher than 0.010.

  FIG. 7 is a photograph (SEM photograph) taken of the surface of the core 11 using the SEM before forming the shell layer 12 with respect to the toner B. FIG. 8 is a photograph (SEM photograph) obtained by photographing the surface of the shell layer 12 of the toner particles 10 contained in the toner B using an SEM. Specifically, among the toner particles 10 included in each of the toners B to G, the surface of the shell layer 12 of the toner particles 10 having a diameter of 6 μm to 8 μm was photographed using an SEM. As a result, FIG. 8 (SEM photograph) was taken with respect to toner B, and SEM photographs substantially similar to the SEM photograph of toner B (FIG. 8) were also taken with respect to toners C to G.

  As shown in FIG. 7, the particles adhered to the surface of the core 11 before the shell layer 12 was formed. On the other hand, as shown in FIG. 8, no particles adhered to the surface of the shell layer 12. As described above, when the surface of the shell layer 12 of the toner particles 10 having a diameter of 6 μm or more and 8 μm or less among the toner particles 10 included in each of the toners B to G is observed using the SEM, the formation of the shell layer 12 is formed. There were no substantially spherical particles (particulate charge control agent) derived from the resin particles used. Further, as shown in FIG. 8, the shell layer 12 was formed on the entire surface of the core 11. Further, the surface of the shell layer 12 was smooth.

  FIG. 9 is a photograph (TEM photograph) obtained by photographing a cross section of the toner particles 10 contained in a toner (toner according to a comparative example) prepared by a method different from the toners B to G using a TEM. FIG. 10 is a photograph (TEM photograph) obtained by photographing a cross section of the toner particles 10 contained in the toner B using a TEM. Specifically, among the toner particles 10 included in each of the toners B to G, a cross section of the toner particles 10 having a diameter of 6 μm to 8 μm was photographed using a TEM. As a result, FIG. 10 (TEM photograph) was taken with respect to the toner B, and TEM photographs substantially similar to the TEM photograph of the toner B (FIG. 10) were taken with respect to the toners C to G.

  As shown in FIG. 9, in the toner according to the comparative example, the shell layer 12 was not formed into a film. On the other hand, as shown in FIG. 10, in each of the toners B to G, the shell layer 12 was formed into a film, and a clear boundary surface was observed between the core 11 and the shell layer 12. Thus, among the toner particles 10 contained in each of the toners B to G, when a cross section of the toner particles 10 having a diameter of 6 μm to 8 μm is observed using a TEM, the gap between the core 11 and the shell layer 12 is observed. There was a clear boundary surface.

  Further, as shown in FIG. 10, among the toner particles 10 included in each of the toners B to G, when the cross section of the shell layer 12 of the toner particles 10 having a diameter of 6 μm or more and 8 μm or less is observed using a TEM, There were no cracks in a direction substantially perpendicular to the surface of the core 11.

  As described above, in each of the toners B to G, the shell layer 12 contained a resin and a charge control agent of 0.3% by mass to 10.0% by mass with respect to the mass of the resin. Moreover, the core 11 did not contain a charge control agent. Even when no charge control agent was used in the formation of the core 11, the toners B to G each had excellent chargeability (charge amount). In each of the toners B to G, the core 11 was completely covered with the shell layer 12. The average thickness of the shell layer 12 in each of the toners B to G was 200 nm or more and 250 nm or less. Each of the toners B to G was excellent in both fixability (maximum fixable temperature and minimum fixable temperature) and storage stability (cohesion degree). The reason is considered to be that the release of the release agent and the aggregation of the toner particles can be suppressed.

  In each of the production methods of the toners B to G, an aqueous emulsion containing resin particles containing a charge control agent of 0.3% by mass or more and 10.0% by mass or less with respect to the mass of the resin was sprayed. As a result, toners B to G having excellent chargeability (charge amount) could be manufactured. Even if no charge control agent was used in the formation of the core 11, toners B to G having excellent chargeability could be produced.

  In each of the manufacturing methods of the toners B to G, when forming the shell layer 12, the aqueous emulsion was sprayed into an air stream having a flow rate of 30 m / second or more in which the core 11 was dispersed. Thus, toners B to G excellent in both fixability (maximum fixable temperature and minimum fixable temperature) and storage stability (aggregation degree) could be produced.

  In each of the production methods of the toners B to G, the aqueous emulsion contained a surfactant (sodium lauryl sulfate). Thereby, it is considered that the shell layer 12 is easily formed uniformly on the surface of the core 11.

  In each of the production methods of the toners B to G, the solid content concentration of the aqueous emulsion was 5% by mass or more and 50% by mass or less (specifically, 15% by mass). Thereby, it is considered that the surface of the core 11 is easily covered with the resin particles (shell layer 12).

The present invention is not limited to the above embodiments.
When forming the shell layer of the toner, the aqueous emulsion is sprayed into an air stream having a flow rate of 30 m / second or more in which the core is dispersed, and the aqueous emulsion is 0.3% by mass or more and 10.0% by mass with respect to the mass of the resin. When the resin particles containing the following charge control agent are included, a toner having excellent chargeability can be produced.

  Further, when the toner shell layer contains a resin and a charge control agent of 0.3% by mass or more and 10.0% by mass or less with respect to the mass of the resin, the toner has excellent chargeability. .

  The toner according to the present invention can be used for forming an image in, for example, a copying machine or a printer.

DESCRIPTION OF SYMBOLS 10 Toner particle 11 Core 11a Binder resin 11b Internal additive 12 Shell layer 13 External additive 100 Surface modification apparatus 101 Powder flow path 101a, 101b End part 102 Stirring chamber 103 Spray part 104 Powder input part 104a Input port 104b Electromagnetic valve 105 Powder recovery unit 105a Recovery tank 105b Electromagnetic valve 110 Stirrer 110a Blade

Claims (7)

Forming a core;
Forming a shell layer on the surface of the core;
Including
In the step of forming the shell layer, an aqueous emulsion is sprayed in an air current having a flow velocity of 30 m / second or more in which the core is dispersed,
The aqueous emulsion includes resin particles containing a charge control agent in an amount of 0.3% by mass or more and 10.0% by mass or less based on the mass of the resin,
The air flow circulates in an annular flow path,
The aqueous emulsion includes a surfactant,
The solid content concentration of the aqueous emulsion is 5% by mass or more and 50% by mass or less,
The core contains a polyester resin as a binder resin,
The resin contained in the resin particles is a styrene acrylic resin,
The toner production method, wherein the charge control agent contained in the resin particles is a nigrosine compound. The toner manufacturing method according to claim 1 , wherein the core does not contain a charge control agent. The formed shell layer contains a resin and a charge control agent of 0.3% by mass to 10.0% by mass with respect to the mass of the resin ,
The resin containing the previous SL shell layer is the styrene-acrylic resin,
The charge control agent, wherein the shell layer contains, the a nigrosine compound, method for producing a toner according to claim 1 or 2. Forming the shell layer on the surface of the core to obtain a plurality of toner particles;
Among the obtained plurality of toner particles, the shell layer of the following toner particles 8μm or more in diameter 6μm has no cracks in the direction substantially perpendicular to the surface of the core, any one of claims 1 to 3 2. A method for producing the toner according to 1 . Forming the shell layer on the surface of the core to obtain a plurality of toner particles;
Among the obtained plurality of toner particles, there is no particulate of the charge control agent on the surface of the shell layer of the following toner particles 8μm or more in diameter 6 [mu] m, according to any one of claims 1-4 Toner manufacturing method . Forming the shell layer on the surface of the core to obtain a plurality of toner particles;
Among the obtained plurality of toner particles, the following toner particle or the diameter 6 [mu] m 8 [mu] m, the production of the toner according to any one of having a boundary surface, according to claim 1 to 5 between the core and the shell layer Way . The glass transition point of the polyester resin is 58 ° C.,
The glass transition point of the styrene-acrylic resin is 62 ° C., method for producing a toner according to any one of claims 1-6.