toner

Abstract

To provide a toner that improves adhesion between a core and a shell, prevents peeling of the shell even in use over a long period, and has excellent developability for a long period.SOLUTION: A toner has a toner particle that has a core particle having a resin component and a shell on the surface of the core particle. The resin component contains a polyester resin having a monomer unit having a heterocyclic group in an amount of more than 50.0 mass% in the resin component, and the shell is at least one resin selected from the group consisting of a specific (meth)acrylic resin and a melamine resin.SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present disclosure relates to a toner used to form a toner image by developing an electrostatic latent image formed by electrophotography, electrostatic recording, toner jet recording, or the like. [Background technology]

[0002] As electrophotographic technology used in copiers, printers, facsimile receiving devices, etc. advances, user demands are becoming increasingly stringent. In recent years, there has been a strong demand for compact designs that can produce high-quality prints over a long period of time. From the perspective of compact design, attempts are being made to achieve miniaturization by simplifying and simplifying fixing components such as heat rollers and films that fix toner images to transfer materials. This approach requires fixing to be possible without heating the fixing components as much as possible, so binder resins with low melting points and glass transition points, as well as release agents with low melting points, are often used to produce toners with excellent low-temperature fixing properties. Therefore, when such toners are stored at high temperatures, the toner particles tend to fuse together, which is a problem. To address the above-mentioned problems, for example, Patent Document 1 discloses a core-shell toner in which a thermosetting resin or a thermoplastic resin is used for the shell layer. [Prior art documents] [Patent documents]

[0003] [Patent Document 1] Japanese Patent Application Laid-Open No. 2015-045844 Summary of the Invention [Problem to be solved by the invention]

[0004] However, from the viewpoint of enabling good printing over a long period of time, if the above-mentioned toner is used for repeated printing, the shell of the core-shell toner may peel off from the core. As a result, the charging property may be disturbed, and the peeled shell or exposed core may cause contamination or fusion to the developing member or charging member, resulting in poor images. In other words, it has been found that the above-mentioned core-shell toner has a problem in terms of durability. In order to provide an image forming apparatus that is capable of producing good printing over a long period of time while having a compact design as required by the market, improvements in the various properties of toner are still required. The present disclosure provides a toner that has improved adhesion between the core and shell, suppresses shell peeling even during long-term use, and provides excellent developability over a long period of time. [Means for solving the problem]

[0005] A toner having core particles having a resin component and a shell on the surface of the core particles, the toner particles are particles obtained by forming the shell on the surface of the core particles in an aqueous medium in which the core particles are dispersed, The resin component has the following formula (1 -2 ) and a monomer unit derived from an aliphatic diol, in an amount of more than 50.0 mass% in the resin component, The toner is characterized in that the shell comprises a (meth)acrylic resin having at least one monomer unit selected from the group consisting of the following formulae (2) and (3): ( In formula (1-2), R 5 each independently represents a linear or branched alkylene group having 2 to 8 carbon atoms, m and n each independently represents 0 or an integer of 1 to 5, and m+n satisfies 1 to 10. In the following formula (2), R 2 represents hydrogen or a methyl group. In the following formula (3), R 3 represents hydrogen or a methyl group, and R 4 represents an alkylene group having 1 to 3 carbon atoms.

[0006] [ka] [Effects of the Invention]

[0007] According to the present disclosure, it is possible to provide a toner that has improved adhesion between the core and shell, suppresses peeling of the shell even during long-term use, and exhibits excellent developability over a long period of time. DETAILED DESCRIPTION OF THE INVENTION

[0008] The expressions "XX or more and YY or less" or "XX to YY" that represent a numerical range mean a numerical range including the endpoints, that is, the lower limit and the upper limit, unless otherwise specified. When numerical ranges are stated in stages, the upper and lower limits of each numerical range can be combined in any way. The (meth)acrylic acid ester means an acrylic acid ester and / or a methacrylic acid ester. "Monomer unit" refers to the reacted form of a monomeric substance in a polymer.

[0009] The inventors have discovered that by using core particles whose main component is a polyester resin having a specific component and a shell having a specific component, the adhesion between the core particles and the shell is improved, and peeling of the shell is suppressed even during long-term use. Specifically, in a toner having core particles having a resin component and toner particles having a shell on the surface of the core particles, the resin component of the core particles must contain more than 50.0 mass % of a polyester resin having a monomer unit represented by formula (1). The monomer unit represented by formula (1) is a monomer unit obtained by condensation polymerization of a heterocyclic diol. The shell comprises at least one resin selected from the group consisting of the following (A) and (B): (A) A (meth)acrylic resin having at least one monomer unit selected from the group consisting of formula (2) and formula (3). (B) Melamine resin

[0010] [ka]

[0011] In formula (1), R 1 represents a heterocyclic group having at least one heteroatom selected from the group consisting of oxygen, nitrogen, and sulfur. In formula (2), R 2 represents hydrogen or a methyl group. In formula (3), R 3 represents hydrogen or a methyl group, and R 4 represents an alkylene group having 1 to 3 carbon atoms (more preferably 2 or 3).

[0012] The present inventors believe that the detailed mechanism is as follows. When a polyester resin containing a monomer unit derived from a heterocyclic diol represented by formula (1) is used as the resin component of a core particle, the heteroatom in the heterocyclic structure polarizes the polyester resin, resulting in high polarity. Furthermore, because formula (1) has a rigid cyclic structure, it is thought that the heteroatom with high polarity is easily exposed at the interface between the core particle and the shell. When the above-mentioned (meth)acrylic resin or melamine resin is used for the shell, these resins form hydrogen bonds with heteroatoms of the resin component of the core particle, and the adhesion between the core particle and the shell is improved due to intermolecular interactions. As a result, it is possible to suppress peeling of the shell even during long-term use. By suppressing peeling of the shell, it is possible to obtain a toner having excellent durability in which development problems such as fog and streaks can be suppressed over a long period of time.

[0013] The resin component of the core particle contains a polyester resin having a monomer unit represented by formula (1) in an amount of more than 50.0 mass % of the resin component of the core particle. If the content is within the above range, the adhesion between the core particles and the shell is improved and peeling of the shell is suppressed even during long-term use, more preferably 55.0% by mass or more, and even more preferably 60.0% by mass or more. There is no particular upper limit, but it is preferably 100.0% by mass or less, more preferably 98.0% by mass or less, and even more preferably 95.0% by mass or less.

[0014] The content of the heterocyclic diol-derived monomer unit represented by formula (1) in the polyester resin is preferably 5.0% by mass to 35.0% by mass. Within this range, the glass transition temperature of the resin can be adjusted to an appropriate temperature, while sufficient intermolecular interaction necessary for adhesion between the core particle and the shell can be obtained. A more preferred range is 20.0% by mass to 35.0% by mass.

[0015] The heterocyclic diols capable of forming the monomer unit represented by formula (1) include spiro glycol, isosorbide, or derivatives thereof. Among these, isosorbide and its alkylene oxide adduct are preferred, as isosorbide and its alkylene oxide adduct provide excellent charge build-up and are easy to suppress initial fogging. R 1 is preferably a heterocyclic group having oxygen. The monomer unit represented by formula (1) is more preferably represented by at least one selected from the group consisting of the following formulas (1-2) and (1-3), and even more preferably represented by the following formula (1-2).

[0016] [ka]

[0017] In formula (1-2), R 5each independently represents a linear or branched alkylene group having 2 to 8 carbon atoms (more preferably 2 or 3). m and n each independently represent 0 or an integer of 1 to 5, and m+n satisfies 0 to 10. m and n are more preferably 0. In formula (1-3), R 6 are each independently a hydrogen atom or a methyl group.

[0018] In addition to the monomer unit represented by formula (1), the polyester resin preferably contains at least one selected from the group consisting of a structure in which an aliphatic diol is condensed with a carboxylic acid component (preferably a dicarboxylic acid or a tricarboxylic acid) and a structure in which an alicyclic diol is condensed with a carboxylic acid component (preferably a dicarboxylic acid or a tricarboxylic acid), and more preferably contains a structure in which an aliphatic diol is condensed with a carboxylic acid component. The aliphatic diol may be at least one selected from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, 1,4-cyclohexanedimethanol, dipropylene glycol, polyethylene glycol, polypropylene glycol, polytetramethylene glycol, sorbitol, 1,2,3,6-hexanetetrol, 1,4-sorbitan, pentaerythritol, dipentaerythritol, tripentaerythritol, 1,2,4-butanetriol, 1,2,5-pentanetriol, glycerin, 2-methylpropanetriol, and 2-methyl-1,2,4-butanetriol. The alicyclic diol may be at least one selected from the group consisting of 1,2-cyclohexanediol, 1,3-cyclohexanediol, 1,4-cyclohexanediol, 1,4-cyclohexanedimethanol, 4-(2-hydroxyethyl)cyclohexanol, 4-(hydroxymethyl)cyclohexanol, 4,4'-bicyclohexanol, 2-cyclohexene-1,4-diol, 4-cyclohexene-1,2-dimethanol, 5-norbornene-2,3-dimethanol, and 5-norbornene-2,3-diol. Examples include:

[0019] Examples of acid monomers include aromatic dicarboxylic acids or anhydrides thereof, such as phthalic acid, isophthalic acid, and terephthalic acid; alkyl dicarboxylic acids or anhydrides thereof, such as succinic acid, adipic acid, sebacic acid, and azelaic acid; succinic acid or anhydrides thereof substituted with an alkyl or alkenyl group having 6 to 18 carbon atoms; and unsaturated dicarboxylic acids or anhydrides thereof, such as fumaric acid, maleic acid, and citraconic acid. Among these, preferred acid monomer components include polycarboxylic acids such as terephthalic acid, succinic acid, adipic acid, fumaric acid, trimellitic acid, pyromellitic acid, benzophenonetetracarboxylic acid and anhydrides thereof. The weight average molecular weight Mw of the polyester resin is preferably 20,000 to 100,000.

[0020] The toner particles have a shell on the surface of a core particle. The shell does not necessarily cover the entire core particle, and the core particle may be partially exposed on the surface of the toner particle. The shell needs to be made of a (meth)acrylic resin having at least one monomer unit selected from the group consisting of formula (2) and formula (3), and / or a melamine resin, in order to improve the adhesion between the resin component of the core particle and the shell due to the above-mentioned interaction. Among these, it is preferable that the shell is a (meth)acrylic resin having at least one monomer unit selected from the group consisting of formula (2) and formula (3).

[0021] The melamine resin is preferably at least one selected from the group consisting of methylol melamine resin, hexamethylol melamine resin, and methoxymethylol melamine resin, and more preferably hexamethylol melamine resin.

[0022] The (meth)acrylic monomers that form the monomer unit of formula (2) are acrylic acid and methacrylic acid. Preferred examples of the (meth)acrylic monomer that forms the monomer unit of formula (3) include 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl acrylate, and 2-hydroxypropyl methacrylate. The (meth)acrylic resin has a monomer unit formed by the reaction of (meth)acrylic acid or a (meth)acrylic acid ester. The (meth)acrylic resin is not limited to (meth)acrylic acid or a (meth)acrylic acid ester, and a monomer having an ethylenically unsaturated bond can also be used.

[0023] The shell resin may contain radically copolymerizable monomers in addition to the above monomers. For example, styrene derivatives such as styrene, α-methylstyrene, β-methylstyrene, o-methylstyrene, m-methylstyrene, p-methylstyrene, 2,4-dimethylstyrene, pn-butylstyrene, p-tert-butylstyrene, pn-hexylstyrene, pn-octylstyrene, pn-nonylstyrene, pn-decylstyrene, pn-dodecylstyrene, p-methoxystyrene, and p-phenylstyrene; acrylic acid ester monomers such as methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate, n-butyl acrylate, isobutyl acrylate, tert-butyl acrylate, n-amyl acrylate, n-hexyl acrylate, 2-ethylhexyl acrylate, n-octyl acrylate, n-nonyl acrylate, cyclohexyl acrylate, and benzyl acrylate; Methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, iso-propyl methacrylate, n-butyl methacrylate, iso-butyl methacrylate methacrylic acid ester monomers such as tert-butyl methacrylate, n-amyl methacrylate, n-hexyl methacrylate, 2-ethylhexyl methacrylate, n-octyl methacrylate, and n-nonyl methacrylate. Furthermore, di(meth)acrylates such as ethylene glycol di(meth)acrylate, 1,3-butanediol di(meth)acrylate, and 1,6-hexanediol di(meth)acrylate may also be used.

[0024] Among the above, styrene is preferred, that is, the (meth)acrylic resin is preferably a styrene-(meth)acrylic resin having a monomer unit formed by reaction of styrene as a constituent component. The total content of at least one monomer unit selected from the group consisting of formula (2) and formula (3) in the (meth)acrylic resin is preferably 5.0% to 35.0% by mass. This range provides excellent charging characteristics and sufficient intermolecular interaction necessary for adhesion between the core particle and the shell. A more preferred range is 10.0% to 25.0% by mass. The content of the shell is preferably 0.5 to 3.0 parts by mass relative to 100.0 parts by mass of the resin component of the core particles. Within this range, the shell does not inhibit fixation and the toner has excellent storage stability. The content is more preferably 0.7 to 2.5 parts by mass, and even more preferably 0.7 to 1.5 parts by mass.

[0025] [Resin component of core particles] The resin component of the core particle may contain more than 50.0% by mass of a polyester resin having a monomer unit represented by the above formula (1), and other resins may be used in combination. For example, the following resins can be used.

[0026] For example, homopolymers of styrene and its substituted derivatives such as polystyrene, poly-p-chlorostyrene, and polyvinyltoluene; styrene-p-chlorostyrene copolymer, styrene-vinyltoluene copolymer, styrene-vinylnaphthalene copolymer, styrene-acrylic acid ester copolymer, styrene-methacrylic acid ester copolymer, styrene-α-chloromethyl methacrylate copolymer, styrene-acrylonitrile copolymer, styrene-vinyl methyl ether copolymer, styrene-vinyl ethyl ether copolymer, styrene-vinyl methyl ketone copolymer, and styrene-acrylonitrile-indene copolymer; polyvinyl chloride, phenolic resin, natural resin-modified phenolic resin, natural resin-modified maleic acid resin, acrylic resin, methacrylic resin, polyvinyl acetate, silicone resin, amorphous polyester, crystalline polyester, polyurethane resin, polyamide resin, furan resin, epoxy resin, xylene resin, polyvinyl butyral, terpene resin, coumarone-indene resin, petroleum-based resin, and the like can be used.

[0027] The resin component of the core particle preferably contains a styrene-acrylic resin such as a styrene-acrylic acid ester copolymer or a styrene-methacrylic acid ester copolymer. The styrene-acrylic resin may be made of the above-mentioned styrene derivatives, acrylic acid ester monomers, and methacrylic acid ester monomers. The above-mentioned diacrylate may also be used. The content of the styrene acrylic resin in the resin component of the core particle is preferably 2.0% by mass or more and less than 50.0% by mass, and more preferably 5.0% by mass or more and 45.0% by mass or less.

[0028] [Coloring agent] The toner particles preferably contain a colorant. Examples of the colorant include the following: Examples of black colorants include carbon black and those toned to black using a yellow colorant, a magenta colorant, and a cyan colorant. As the colorant, a pigment may be used alone, but it is more preferable to use a dye and a pigment in combination to improve the clarity from the viewpoint of the image quality of a full-color image. Magenta colored pigments include the following: CI Pigment Red 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 21, 22, 23, 30, 31, 32, 37, 38, 39, 40, 41, 48:2, 48:3, 48:4, 49, 50, 51, 52, 53, 54, 55, 57:1, 58, 60, 63, 64, 68, 81:1, 83, 87, 88, 89, 90, 112, 114, 122, 123, 146, 147, 150, 163, 184, 202, 206, 207, 209, 238, 269, 282; CI Pigment Violet 19; CI Bat Red 1, 2, 10, 13, 15, 23, 29, 35. Magenta-colored dyes include solvent dyes such as CI Solvent Red 1, 3, 8, 23, 24, 25, 27, 30, 49, 81, 82, 83, 84, 100, 109, and 121; CI Disperse Red 9; CI Solvent Violet 8, 13, 14, 21, and 27; and CI Disperse Violet 1; and basic dyes such as CI Basic Red 1, 2, 9, 12, 13, 14, 15, 17, 18, 22, 23, 24, 27, 29, 32, 34, 35, 36, 37, 38, 39, and 40; and CI Basic Violet 1, 3, 7, 10, 14, 15, 21, 25, 26, 27, and 28.

[0029] Cyan coloring pigments include the following: CI Pigment Blue 2, 3, 15:2, 15:3, 15:4, 16, 17; CI Vat Blue 6; CI Acid Blue 45; and copper phthalocyanine pigments having 1 to 5 phthalimidomethyl groups substituted on the phthalocyanine skeleton. Cyan coloring dyes include CI Solvent Blue 70. Yellow coloring pigments include the following: CI Pigment Yellow 1, 2, 3, 4, 5, 6, 7, 10, 11, 12, 13, 14, 15, 16, 17, 23, 62, 65, 73, 74, 83, 93, 94, 95, 97, 109, 110, 111, 120, 127, 128, 129, 147, 151, 154, 155, 168, 174, 175, 176, 180, 181, 185; CI Vat Yellow 1, 3, 20. Yellow coloring dyes include CI Solvent Yellow 162. The amount of the colorant used is preferably 0.1 parts by mass or more and 30.0 parts by mass or less with respect to 100.0 parts by mass of the binder resin.

[0030] [wax] The toner particles preferably contain a wax. The wax is not particularly limited, but examples thereof include the following. Hydrocarbon waxes such as low molecular weight polyethylene, low molecular weight polypropylene, alkylene copolymers, microcrystalline wax, paraffin wax, and Fischer-Tropsch wax; oxides of hydrocarbon waxes such as oxidized polyethylene wax or their block copolymers; waxes whose main component is fatty acid esters such as carnauba wax; partially or completely deoxidized fatty acid esters such as deoxidized carnauba wax. Further examples include the following: saturated straight-chain fatty acids such as palmitic acid, stearic acid, and montanic acid; unsaturated fatty acids such as brassidic acid, eleostearic acid, and parinaric acid; saturated alcohols such as stearyl alcohol, aralkyl alcohol, behenyl alcohol, carnaubyl alcohol, ceryl alcohol, and melissyl alcohol; polyhydric alcohols such as sorbitol; and fatty acids such as palmitic acid, stearic acid, behenic acid, and montanic acid mixed with alcohols such as stearyl alcohol, aralkyl alcohol, behenyl alcohol, carnaubyl alcohol, ceryl alcohol, and melissyl alcohol. Esters; fatty acid amides such as linoleic acid amide, oleic acid amide, and lauric acid amide; saturated fatty acid bisamides such as methylene bisstearic acid amide, ethylene biscapric acid amide, ethylene bislauric acid amide, and hexamethylene bisstearic acid amide; unsaturated fatty acid amides such as ethylene bisoleic acid amide, hexamethylene bisoleic acid amide, N,N'-dioleyl adipamide, and N,N'-dioleyl sebacic acid amide; aromatic bisamides such as m-xylene bisstearic acid amide and N,N'-distearyl isophthalamide; fatty acid metal salts (commonly known as metal soaps) such as calcium stearate, calcium laurate, zinc stearate, and magnesium stearate; waxes grafted onto aliphatic hydrocarbon waxes with vinyl monomers such as styrene and acrylic acid; partial esters of fatty acids and polyhydric alcohols, such as behenic acid monoglyceride; and methyl ester compounds having hydroxyl groups obtained by hydrogenating vegetable oils and fats.

[0031] Among these waxes, hydrocarbon waxes such as paraffin wax and Fischer-Tropsch wax, and ester wax are preferred from the viewpoint of improving low-temperature fixability and anti-wrapping properties after fixation. The content of the wax is preferably 0.5 parts by mass or more and 25.0 parts by mass or less with respect to 100.0 parts by mass of the binder resin. Furthermore, from the viewpoint of achieving both the storage stability and high-temperature offset resistance of the toner, it is preferable that the peak temperature of the maximum endothermic peak of the wax present in the temperature range of 30°C to 200°C in an endothermic curve during temperature rise measured with a differential scanning calorimeter (DSC) is 50°C to 110°C.

[0032] [Charge control agent] The toner may contain a charge control agent as needed. Known charge control agents can be used. The charge control agent may be added internally or externally to the toner particles. The amount of charge control agent added is preferably 0.2 parts by mass or more and 10.0 parts by mass or less per 100.0 parts by mass of the binder resin.

[0033] The toner may be used as a one-component developer. In terms of obtaining stable images over a long period of time, the toner may be mixed with a magnetic carrier and used as a two-component developer. [Career] The magnetic carrier may be any of the following known magnetic carriers: For example, surface-oxidized or unoxidized iron powder, metal particles of iron, lithium, calcium, magnesium, nickel, copper, zinc, cobalt, manganese, rare earth elements, etc., alloy particles thereof, oxide particles, magnetic materials such as ferrite, and magnetic material-dispersed resin carriers (so-called resin carriers) containing magnetic materials and a binder resin that holds the magnetic materials in a dispersed state. When the toner is mixed with a magnetic carrier to be used as a two-component developer, good results are usually obtained when the carrier mixing ratio is, in terms of toner concentration in the two-component developer, preferably 2% by mass or more and 15% by mass or less, and more preferably 4% by mass or more and 13% by mass or less.

[0034] The method for producing the toner particles is not particularly limited as long as it is a known production method such as an emulsion aggregation method, a pulverization method, or a dissolution suspension method. The production method using the pulverization method will be described below. In the pulverization method, a resin component and, if necessary, optional components such as a colorant, a wax, and a charge control agent are mixed, and the resulting mixture is melt-kneaded. Subsequently, the resulting melt-kneaded product is pulverized and classified to obtain core particles having a desired particle size.

[0035] The formation of a shell covering the core particles is carried out by adding a material for forming the shell in an aqueous solution. The material for forming the shell is preferably added in the form of a dispersion of resin particles. After adding the core particles to the aqueous medium, the core particles are dispersed in the aqueous medium. Dispersion methods include a method in which the core particles are mechanically dispersed in the aqueous medium using an apparatus capable of vigorously stirring the dispersion, and a method in which the core particles are dispersed in an aqueous medium containing a dispersant. The method using a dispersant is advantageous in that the core particles are uniformly dispersed in the aqueous medium, making it easy to form a shell without exposing the surface of the core particles.

[0036] As a device capable of vigorously stirring the dispersion, a device such as Hibismix (manufactured by Primix Co., Ltd.) is preferred. The shell can be formed by adding a material for forming the shell, adhering it to the core particles, and then increasing the temperature. The temperature at which the shell layer is formed is preferably 65°C or higher and 95°C or lower, and more preferably 70°C or higher and 90°C or lower. By forming the shell layer at a temperature within this range, the formation of the shell layer proceeds smoothly while preventing the toner particles from coalescing.

[0037] After the shell is formed as described above, the dispersion containing the core particles coated with the shell is cooled to room temperature to obtain a dispersion of toner particles. Thereafter, if necessary, the toner particles are washed in a washing step and dried in a drying step to obtain toner particles. The weight average particle size of the toner particles is preferably 4.0 μm to 8.0 μm.

[0038] The toner particles may be used as they are as a toner. If necessary, an external additive may be attached to the surface of the toner particles to form a toner. A preferred method is to mix the toner particles and the external additive using a mixer such as an FM mixer (manufactured by Nippon Coke & Engineering Co., Ltd.) while adjusting the conditions so that the external additive is not embedded in the surface of the toner particles.

[0039] The methods for measuring various physical properties will be described below. <Identification of resins contained in the core and shell> The composition and ratio of the constituent compounds of the resin contained in the core and shell are identified using a pyrolysis gas chromatography mass spectrometer (hereinafter also referred to as "pyrolysis GC / MS") and NMR. Note that if the resin contained in the core and shell is available separately, it can also be measured separately.

[0040] Pyrolysis GC / MS is used to analyze the types of constituent compounds in resins. The types of constituent compounds are identified by analyzing the mass spectrum of the components of the resin decomposition products that are produced when the resin is thermally decomposed at 550°C to 700°C. The specific measurement conditions are as follows: [Pyrolysis GC / MS measurement conditions] Pyrolysis device: JPS-700 (Japan Analysis Industry) Decomposition temperature: 590℃ GC / MS equipment: Focus GC / ISQ (Thermo Fisher) Column: HP-5MS, length 60 m, inner diameter 0.25 mm, film thickness 0.25 μm Inlet temperature: 200℃ Flow pressure: 100kPa Split: 50mL / min MS ionization: EI Ion source temperature: 200℃ Mass Range 45-650

[0041] The abundance ratio of the identified resin constituent compounds was then determined by 1 The structure is determined by nuclear magnetic resonance spectroscopy ( 1 H-NMR) [400MHz, CDCl3, room temperature ( 25°C)]. Measuring device: FT NMR device JNM-EX400 (manufactured by JEOL Ltd.) Measurement frequency: 400MHz Pulse condition: 5.0 μs Frequency range: 10500Hz Number of times accumulated: 1024 The molar ratio of each monomer component is determined from the integral value of the obtained spectrum, and the composition ratio (mass %) is calculated based on this.

[0042] [Method for measuring weight average particle size (D4) of toner particles] The weight-average particle size (D4) of the toner particles is measured with an effective number of 25,000 measurement channels using a precision particle size distribution measuring device equipped with a 100 μm aperture tube and using the narrow-pore electrical resistance method, "Coulter Counter Multisizer 3" (registered trademark, manufactured by Beckman Coulter, Inc.), and the accompanying dedicated software "Beckman Coulter Multisizer 3 Version 3.51" (manufactured by Beckman Coulter, Inc.), for setting measurement conditions and analyzing measurement data, and the weight-average particle size (D4) is calculated by analyzing the measurement data. The aqueous electrolyte solution used for the measurement is prepared by dissolving special grade sodium chloride in ion-exchanged water to a concentration of approximately 1% by mass, such as "ISOTON II" (manufactured by Beckman Coulter, Inc.). Before carrying out the measurements and analysis, the dedicated software is set up as follows. In the "Change Standard Measurement Method (SOM) screen" of the dedicated software, set the total count in control mode to 50,000 particles, the number of measurements to 1, and the Kd value to the value obtained using "Standard Particles 10.0 μm" (Beckman Coulter, Inc.). Press the threshold / noise level measurement button to automatically set the threshold and noise level. Also, set the current to 1,600 μA, the gain to 2, the electrolyte to ISOTON II, and check "Flush aperture tube after measurement." In the dedicated software's "Pulse to particle size conversion setting screen," set the bin interval to logarithmic particle size, the particle size bin to 256 particle size bins, and the particle size range to 2 μm or more and 60 μm or less.

[0043] The specific measurement method is as follows. (1) Pour approximately 200 mL of the electrolyte solution into a 250 mL round-bottom glass beaker made specifically for the Multisizer 3, set it on the sample stand, and stir the stirrer rod counterclockwise at 24 revolutions per second. Then, use the "aperture tube flush" function of the dedicated software to remove any dirt and air bubbles from inside the aperture tube. (2) Approximately 30 mL of the above aqueous electrolyte solution is placed in a 100 mL flat-bottom glass beaker, and approximately 0.3 mL of the following dilution solution is added as a dispersant. Diluted solution: "Contaminon N" (a 10% aqueous solution of a pH 7 neutral detergent for cleaning precision measuring instruments, consisting of a nonionic surfactant, an anionic surfactant, and an organic builder, manufactured by Wako Pure Chemical Industries, Ltd.) diluted 3 times by mass with ion-exchanged water. (3) A predetermined amount of ion-exchanged water is placed in the water tank of the ultrasonic disperser described below, which has two built-in oscillators with an oscillation frequency of 50 kHz and a phase difference of 180 degrees and an electrical output of 120 W, and approximately 2 mL of the Contaminon N is added to this water tank. Ultrasonic disperser: "Ultrasonic Dispersion System Tetora150" (manufactured by Nikkaki Bios Co., Ltd.) (4) Set the beaker (2) in the beaker fixing hole of the ultrasonic disperser, operate the ultrasonic disperser, and adjust the height of the beaker so that the resonance state of the liquid surface of the electrolytic solution in the beaker is maximized. (5) While the electrolyte solution in the beaker in (4) is being irradiated with ultrasonic waves, approximately 10 mg of toner is added little by little to the electrolyte solution and dispersed. Then, the ultrasonic dispersion process is continued for another 60 seconds. During the ultrasonic dispersion, the water temperature in the water tank is set to 15°C or higher and 40°C or lower. Adjust as necessary. (6) Using a pipette, the electrolytic solution (5) containing the dispersed toner is dropped into the round-bottom beaker (1) placed in the sample stand, and the measurement concentration is adjusted to approximately 5%. Then, measurements are continued until the number of particles measured reaches 50,000. (7) The measurement data is analyzed using the dedicated software provided with the device, and the weight-average particle size (D4) is calculated. Note that when the dedicated software is set to Graph / Volume %, the "Average diameter" on the Analysis / Volume Statistics (Arithmetic Mean) screen is the weight-average particle size (D4). [Example]

[0044] The present invention will be described in more detail below with reference to examples. The present invention is not limited to the following examples. Note that the number of parts in the examples and comparative examples is based on mass unless otherwise specified.

[0045] <Production of Polyester Resin 1 for Core Particles> Into a reaction vessel equipped with a stirrer, a thermometer, a nitrogen inlet tube, a dehydration tube, and a pressure reducing device, 100.0 parts of terephthalic acid, 23.1 parts of trimellitic anhydride, 11.7 parts of adipic acid, 70.4 parts of isosorbide, and 1,3-propane J 42.8 parts of oil was added, and the mixture was heated to a temperature of 130°C with stirring. After adding 0.5 parts of titanium (IV) isopropoxide as an esterification catalyst, the temperature was raised to 160°C and condensation polymerization was carried out over 5 hours. Thereafter, the temperature was raised to 180°C and the reaction was continued under reduced pressure until the desired molecular weight was reached, yielding polyester resin 1. The weight average molecular weight Mw of polyester resin 1 was 50,000.

[0046] <Production of Polyester Resins 2 to 8 for Core Particles> Polyester resins 2 to 8 were produced in the same manner as polyester resin 1, except that the raw materials were changed as shown in Table 1.

[0047] [Table 1] In the table, "amount of formula (1)" indicates the content of the monomer unit represented by formula (1) in the polyester resin.

[0048] <Production of styrene-acrylic resin for core particles> Into a reaction vessel equipped with a stirrer, a thermometer, and a nitrogen inlet tube, 80.0 parts of styrene, 20.0 parts of n-butyl acrylate, and 0.3 parts of hexanediol diacrylate were added and heated to a temperature of 80°C with stirring. Subsequently, 2.0 parts of Perbutyl O (10-hour half-life temperature 72.1°C (manufactured by NOF Corporation)) was added as a polymerization initiator, and polymerization was carried out for 5 hours to obtain a styrene-acrylic resin for core particles.

[0049] <Production of Shell Resin 1> To an aqueous solution prepared by dissolving 3.0 parts of a surfactant, Neogen RK (manufactured by Daiichi Kogyo Seiyaku Co., Ltd.), in 50 parts of ion-exchanged water, 62.8 parts of styrene, 20.9 parts of 2-hydroxyethyl methacrylate, 15.5 parts of n-butyl acrylate, and 0.8 parts of ethylene glycol dimethacrylate were added and dispersed. An aqueous solution of 0.3 parts potassium persulfate dissolved in 10 parts ion-exchanged water was added while slowly stirring for an additional 10 minutes. After nitrogen substitution, emulsion polymerization was carried out at 70°C for 6 hours. After polymerization was completed, the reaction solution was cooled to room temperature, and ion-exchanged water was added to obtain an aqueous dispersion of shell resin 1 (shell resin 1 dispersion) with a solids concentration of 50.0% by mass.

[0050] <Production Examples of Shell Resins 2 to 6> Shell Resins 2 to 6 were obtained in the same manner as in the production example for Shell Resin 1, except that the monomer composition was changed as shown in Table 2.

[0051] [Table 2] In the table, "amount of formula (2) and (3)" indicates the total content of at least one monomer unit selected from the group consisting of formula (2) and formula (3). Abbreviations are as follows: 2-HEMA: 2-hydroxyethyl methacrylate MMA-EG: ethylene glycol dimethacrylate

[0052] <Production of Toner 1> (Production of core particle 1) Polyester resin 1: 90.0 parts Styrene-acrylic resin for core particles: 10.0 parts CI Pigment Blue 15:3 (Copper Phthalocyanine): 5.0 parts Ester wax (behenyl behenate: melting point 72°C) 15.0 parts Fischer-Tropsch wax (Sasol C105, melting point: 105°C): 2.0 copies The above materials were premixed in a Mitsui Henschel mixer (manufactured by Mitsui Miike Chemical Engineering Co., Ltd.), and then melt-kneaded using a twin-screw extruder (trade name: PCM-30, manufactured by Ikegai Iron Works Co., Ltd.) with the temperature set so that the molten temperature at the discharge outlet was 140°C. The resulting kneaded product was cooled, coarsely pulverized using a hammer mill, and then finely pulverized using a pulverizer (product name: Turbo Mill T250, manufactured by Turbo Kogyo Co., Ltd.) The resulting finely pulverized powder was classified using a multi-division classifier utilizing the Coanda effect to obtain core particles 1 having a weight average particle size (D4) of 6.8 μm.

[0053] (Production of Toner Particles 1) To 250.0 parts of ion-exchanged water heated to 40°C, 1.8 parts of tricalcium phosphate was added, and the mixture was stirred at a stirring speed of 15,000 rpm using a TK homomixer (manufactured by Tokushu Kika Kogyo Co., Ltd.) to prepare an aqueous medium. 100.0 parts of core particles 1 were added to an aqueous medium to prepare a slurry of core particles 1. Subsequently, a solidification reaction was carried out to add 1.0 part of shell resin 1 to 100.0 parts of core particles 1. 2.0 parts of a shell resin 1 dispersion having a component concentration of 50.0% by mass was added, and the temperature was raised to 75° C. and maintained at this temperature for 2 hours to form a shell layer on the surface of the core particles. After cooling to room temperature, hydrochloric acid was added to dissolve calcium phosphate as a dispersant, and the mixture was filtered, washed with water, and dried to obtain toner particles 1 having a core-shell structure and a weight average particle size (D4) of 6.8 μm.

[0054] (Toner 1 production) 100.0 parts of toner particles 1 and 1.5 parts of dry silica particles ("AEROSIL (registered trademark) REA90" manufactured by Nippon Aerosil Co., Ltd.: positively charged hydrophobized silica particles) were mixed for 3 minutes using an FM mixer (manufactured by Nippon Coke and Engineering Co., Ltd.) to adhere the silica particles to toner particles 1. The mixture was then sieved through a 300 mesh (openings 48 μm) to obtain toner 1.

[0055] <Production of Toners 2 to 9, 11 to 14, and 17 to 19> Toners 2 to 9, 11 to 14, and 17 to 19 were obtained by the same production method as for Toner 1, except for the changes shown in Table 3.

[0056] <Production of Toner 10> (Production of Toner Particles 10) Dilute hydrochloric acid was added to 250.0 parts of ion-exchanged water heated to a temperature of 30°C, and the pH of the aqueous medium in the flask was adjusted to 4. Subsequently, 1.25 parts of a hexamethylolmelamine prepolymer ("Milben 607" manufactured by Showa Denko KK, solid content concentration 80.0% by mass) was added, and the mixture was stirred to dissolve the hexamethylolmelamine prepolymer in the aqueous medium. Subsequently, 100.0 parts of core particles 1 were added to the aqueous medium, and the mixture was stirred at a rate of 1°C / min. The temperature was raised to 70°C and maintained for 2 hours to form a shell layer on the surface of the core particles. After cooling to room temperature, the particles were filtered, washed with water, and dried to obtain toner particles 10 having a core-shell structure and a weight average particle size (D4) of 6.8 μm.

[0057] (Toner 10 production) 100.0 parts of toner particles 10 and 1.5 parts of dry silica particles ("AEROSIL (registered trademark) REA90" manufactured by Nippon Aerosil Co., Ltd.: positively charged hydrophobized silica particles) were mixed for 3 minutes using an FM mixer (manufactured by Nippon Coke and Engineering Co., Ltd.) to adhere the silica particles to the toner particles 10. The mixture was then sieved through a 300 mesh (openings 48 μm) to obtain toner 10.

[0058] <Production of Toner 15> (Preparation of Polyester Resin Particle Dispersion) Polyester resin 1 200.0 parts 500.0 parts ion-exchanged water The above materials were placed in a stainless steel container, heated to 95°C in a warm bath, and melted. While thoroughly stirring at 7,800 rpm using a homogenizer (IKA Ultra Turrax T50), 0.1 mol / L sodium bicarbonate was added to adjust the pH to above 7.0. Thereafter, a mixed solution of 3.0 parts of sodium dodecylbenzenesulfonate and 297.0 parts of ion-exchanged water was gradually added dropwise to emulsify and disperse the mixture, thereby obtaining a polyester resin particle dispersion. The particle size distribution of this polyester resin particle dispersion was measured using a particle size measuring device (LA-920, manufactured by Horiba, Ltd.), and the number average particle size of the polyester resin particle dispersion contained therein was 0.25 μm, and no coarse particles exceeding 1 μm were observed.

[0059] (Preparation of styrene-acrylic resin particle dispersion) 200.0 parts styrene-acrylic resin for core resin 500.0 parts ion-exchanged water The above materials were placed in a stainless steel container, heated to 95°C in a warm bath, and melted. While thoroughly stirring at 7,800 rpm using a homogenizer (IKA Ultra Turrax T50), 0.1 mol / L sodium bicarbonate was added to raise the pH to above 7.0. After that, a mixed solution of 3.0 parts of sodium dodecylbenzenesulfonate and 297.0 parts of ion-exchanged water was gradually added dropwise to emulsify and disperse the mixture, thereby obtaining a styrene-acrylic resin particle dispersion. The particle size distribution of this styrene-acrylic resin particle dispersion was measured using a particle size analyzer (LA-920, manufactured by Horiba, Ltd.), and the number-average particle size of the styrene-acrylic resin particle dispersion contained therein was 0.25 μm, and no coarse particles exceeding 1 μm were observed.

[0060] (Preparation of Wax Particle Dispersion) 500.0 parts ion-exchanged water Fischer-Tropsch wax (Sasol C105, melting point:105 °C) 250.0 copies The above materials were placed in a stainless steel container, heated to 95°C in a hot bath, and melted. While thoroughly stirring at 7,800 rpm using a homogenizer (IKA Ultra Turrax T50), 0.1 mol / L sodium bicarbonate was added to adjust the pH to above 7.0. Thereafter, a mixed solution of 5.0 parts of sodium dodecylbenzenesulfonate and 245.0 parts of ion-exchanged water was gradually added dropwise to emulsify and disperse the mixture, thereby obtaining a wax particle dispersion. The particle size distribution of this wax particle dispersion was measured using a particle size measuring device (LA-920, manufactured by Horiba, Ltd.), and the number-average particle size of the wax particles contained was 0.35 μm, and no coarse particles exceeding 1 μm were observed.

[0061] (Preparation of Colorant Particle Dispersion) CI Pigment Blue 15:3 100.0 parts Sodium dodecylbenzenesulfonate 5.0 parts 400.0 parts ion-exchanged water The above ingredients were mixed and dispersed using a sand grinder mill. The particle size distribution of the colorant particles contained in this colorant particle dispersion was measured using a particle size analyzer (LA-920, manufactured by Horiba, Ltd.), and the number-average particle size of the colorant particles contained was 0.2 μm, and no coarse particles exceeding 1 μm were observed.

[0062] (Production of core particles 15) Polyester resin particle dispersion 450.0 parts Styrene-acrylic resin particle dispersion 50.0 parts Colorant particle dispersion 50.0 parts Wax particle dispersion 50.0 parts Sodium dodecylbenzenesulfonate 5.0 parts A polyester resin particle dispersion, a styrene-acrylic resin particle dispersion, a wax particle dispersion, and sodium dodecylbenzenesulfonate were charged into a reactor (a 1-liter flask with baffles and anchor blades) and mixed uniformly. Meanwhile, a colorant particle dispersion was mixed uniformly in a 500 mL beaker, and this was gradually added to the reactor while stirring to obtain a mixed dispersion. While stirring the resulting mixed dispersion, 0.5 parts of aluminum sulfate aqueous solution (solid content) was added dropwise to form aggregated particles. After the dropwise addition was completed, the system was purged with nitrogen, and the temperature was maintained at 50°C for 1 hour, and then at 55°C for 1 hour. The temperature was then raised to 90°C and maintained at that temperature for 30 minutes. The temperature was then lowered to 63°C and maintained at that temperature for 3 hours to form fused particles. After the specified time had elapsed, the temperature was lowered to 40°C at a rate of 0.5°C per minute to obtain a dispersion of core particles 15.

[0063] (Production of Toner Particles 15) To 100.0 parts of the solid content of the above-mentioned core particle 15 dispersion, 2.0 parts of shell resin 1 dispersion were added, and the mixture was heated to 75°C and maintained for 2 hours to form a shell layer on the surface of the core particles. After cooling to room temperature, the mixture was filtered, washed with water, and dried to obtain toner particles 15 having a core-shell structure and a weight average particle size (D4) of 6.5 μm.

[0064] (Toner 15 production) 100.0 parts of toner particles 15 and 1.5 parts of dry silica particles ("AEROSIL (registered trademark) REA90" manufactured by Nippon Aerosil Co., Ltd.: positively charged hydrophobized silica particles) were mixed for 3 minutes using an FM mixer (manufactured by Nippon Coke and Engineering Co., Ltd.) to adhere the silica particles to the toner particles 15. The mixture was then sieved through a 300 mesh (openings 48 μm) to obtain toner 15.

[0065] <Production of Toner 16> (Production of Core Particles 16) Polyester resin 1 90.0 parts Styrene-acrylic resin for core resin 10.0 parts CI Pigment Blue 15:3 (Copper Phthalocyanine) 5.0 parts Ester wax (behenyl behenate: melting point 72°C) 15.0 parts Fischer-Tropsch wax (Sasol C105, melting point: 105°C) 2.0 copies Methyl ethyl ketone 100.0 parts Ethyl acetate 100.0 parts The above materials were dispersed for 3 hours using an Attritor (manufactured by Mitsui Kinzoku Co., Ltd.) to obtain a colorant dispersion. Separately, 1.8 parts of tricalcium phosphate was added to 300.0 parts of ion-exchanged water heated to 60°C, and the mixture was stirred at a stirring speed of 10,000 rpm using a TK homomixer (manufactured by Tokushu Kika Kogyo Co., Ltd.) to prepare an aqueous medium. The colorant dispersion was added to the aqueous medium, and the mixture was stirred at a stirring speed of 12,000 rpm using the TK homomixer at 65°C under a N2 atmosphere for 15 minutes to granulate colorant particles. The TK homomixer was then replaced with a conventional propeller mixer, the mixing speed of the mixer was maintained at 150 rpm, the internal temperature was raised to 95°C and held for 3 hours to remove the solvent from the dispersion, and a dispersion of core particles 16 was prepared.

[0066] (Production of Toner Particles 16) 2.0 parts of the shell resin 1 dispersion were added to 100.0 parts of the solid content of the above core particle 16 dispersion, and the mixture was heated to 75°C and maintained for 2 hours to form a shell layer on the surface of the core particles. After cooling to room temperature, hydrochloric acid was added to dissolve calcium phosphate as a dispersant, and the mixture was filtered, washed with water, and dried to obtain toner particles 16 having a weight average particle size (D4) of 6.9 μm and a core-shell structure.

[0067] (Toner 16 production) 100.0 parts of toner particles 16 and 1.5 parts of dry silica particles ("AEROSIL (registered trademark) REA90" manufactured by Nippon Aerosil Co., Ltd.: positively charged hydrophobized silica particles) were mixed for 3 minutes using an FM mixer (manufactured by Nippon Coke and Engineering Co., Ltd.) to adhere the silica particles to the toner particles 16. The mixture was then sieved through a 300 mesh (openings 48 μm) to obtain toner 16.

[0068] [Table 3]

[0069] <Image evaluation> Image evaluation was performed using a commercially available color laser printer (Kyocera Document Solutions Inc.'s "FS-C5250DN") that had been partially modified. The printer was modified so that it could operate with only one color process cartridge installed. The printer was also modified so that the temperature of the fixing unit could be changed as desired. A two-component developer prepared according to the method described below was placed in the developing section of the evaluation machine, and the toner was placed in the toner container of the evaluation machine, and the following image evaluation was performed. [Preparation of two-component developer] A two-component developer was prepared by mixing 100 parts of the developer carrier (carrier for FS-C5250DN) and 10 parts of the toner to be evaluated for 30 minutes using a ball mill. The specific image evaluation items are as follows:

[0070] [Fog] In a low temperature and low humidity environment (15°C, 10% RH) or a high temperature and high humidity environment (temperature 32°C / humidity 85% RH), the reflectance (%) of the non-image area after the printout test of 30,000 sheets of an image with a 1% print rate in the initial and horizontal lines is measured using the REFLECTOMETER MODEL TC- Measurements were taken using a Tokyo Denshoku 6DS (manufactured by Tokyo Denshoku Co., Ltd.). The reflectance obtained was subtracted from the reflectance (%) of unused printout paper (standard paper) measured in the same manner, and the resulting value (%) was used for evaluation. The smaller the value, the more suppressed image fogging. The evaluation was carried out in glossy paper mode using plain paper (HP Brochure Paper 200g, Glossy, HP, 200g / m 2 ) was used. (Evaluation criteria) A: Less than 0.5% B: 0.5% or more and less than 1.5% C: 1.5% or more and less than 3.0% D: 3.0% or more

[0071] [Streaks (developability)] After completing a test of printing 30,000 sheets of horizontal line images with a 1% print ratio in a high temperature and humidity environment (temperature 32°C / humidity 85%RH), the test was carried out on a letter-size XEROX 4200 paper (manufactured by XEROX, 75g / m 2 ) and halftone (toner amount: 0.3 mg / cm 2 The halftone image was inspected for the presence or absence of vertical streaks in the paper ejection direction, and durability was evaluated as follows: (Evaluation criteria) A: Not occurred B: Vertical streaks in the paper ejection direction appear in one to three places on the halftone image. C: Vertical streaks in the paper ejection direction appear in 4 to 6 places on the halftone image. D: Seven or more vertical lines appear in the paper ejection direction on the halftone image, or vertical lines with a width of 0.5 mm or more appear.

[0072] [Fixation] Solid image on transfer material (toner amount: 0.9 mg / cm 2 ) was printed at different fixing temperatures and evaluated according to the following criteria. The fixing temperature was measured on the surface of the fixing roller using a non-contact thermometer. The transfer material was letter-size plain paper (XEROX 4200, manufactured by XEROX Corporation, 75 g / m 2 ) was used. (Evaluation criteria) A: No offset at 140℃ B: Offset occurs at 140℃ C: Offset occurs at 150℃ D: Offset occurs at 160℃

[0073] [Blocking (storage)] 5 g of each toner was placed in a 50 mL resin cup and left to stand for 3 days at a temperature of 60° C. and a humidity of 10% RH, and the presence or absence of agglomerates was examined and evaluated according to the following criteria. (Evaluation criteria) A: No clumps formed B: Slight clumps formed, crumbles when lightly pressed with fingers C: Agglomerates form, but do not crumble when lightly pressed with fingers D: Completely aggregated

[0074] Examples 1 to 16 In Examples 1 to 16, the above evaluations were carried out using Toners 1 to 16, respectively. The evaluation results are shown in Table 4. 8~ 10 is a reference example 8~ Let's say it's 10.

[0075] Comparative Examples 1 to 3 In Comparative Examples 1 to 3, the above evaluations were carried out using toners 17 to 19, respectively. The evaluation results are shown in Table 4.

[0076] [Table 4]

Claims

1. A toner having core particles having a resin component and a shell on the surface of the core particles, the toner particles are particles obtained by forming the shell on the surface of the core particles in an aqueous medium in which the core particles are dispersed, The resin component contains a polyester resin having a monomer unit represented by the following formula (1-2) and a monomer unit derived from an aliphatic diol in an amount of more than 50.0 mass% in the resin component: The toner is characterized in that the shell comprises a (meth)acrylic resin having at least one monomer unit selected from the group consisting of the following formulas (2) and (3): In formula (1-2), R 5 s each independently represent a linear or branched alkylene group having 2 to 8 carbon atoms, m and n each independently represent 0 or an integer of 1 to 5, and m+n satisfies a value of 1 to 10. In formula (2), R ２ represents hydrogen or a methyl group. In formula (3), R ３ represents hydrogen or a methyl group, and R ４ represents an alkylene group having 1 to 3 carbon atoms.

2. 2. The toner according to claim 1, wherein the content of the monomer unit represented by formula (1-2) in the polyester resin is 5.0% by mass to 35.0% by mass.

3. 3. The toner according to claim 1, wherein the shell is the (meth)acrylic resin.

4. 4. The toner according to claim 3, wherein the total content of the at least one monomer unit selected from the group consisting of formula (2) and formula (3) in the (meth)acrylic resin is 5.0% by mass to 35.0% by mass.

5. 5. The toner according to claim 1, wherein the content of the shell is 0.5 parts by mass or more and 3.0 parts by mass or less with respect to 100.0 parts by mass of the resin component of the core particle.

6. 6. The toner according to claim 1, wherein the resin component of the core particle contains a styrene-acrylic resin.

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