Patent Grant
9329509
The present application claims priority under 35 U.S.C. §119 to Japanese Patent Application No. 2013-134258, filed Jun. 26, 2013. The contents of this application are incorporated herein by reference in their entirety.
The present disclosure relates to an electrostatic latent image developing toner.
For energy saving and downsizing of an image forming apparatus, there is a demand for a toner excellent in low-temperature fixability. If a toner excellent in the low-temperature fixability is used, a toner can be satisfactorily fixed on a recording medium even if the temperature of a fixing roller is low.
In order to obtain a toner excellent in the low-temperature fixability, a method for producing a toner by using a binder resin having a low melting point (or a binder resin having a low glass transition point) and a release agent having a low melting point has been proposed. It is, however, difficult to produce a toner excellent in high-temperature preservability by this method. The high-temperature preservability of a toner refers to a property that toner particles contained in the toner are not aggregated even if the toner is stored under a high temperature environment. In a toner poor in the high-temperature preservability, toner particles are liable to aggregate under a high temperature environment. When the toner particles aggregate, the charge amount of the toner particles are likely to be lowered.
For purpose of improving the low-temperature fixability, high-temperature preservability, and blocking resistance of a toner, a toner containing a toner particle having a core-shell structure has been proposed.
In an exemplified toner containing a toner particle having a core-shell structure, a toner core contains a binder resin having a low melting point. Besides, the toner core is coated with a shell layer made of a resin. In addition, the resin constituting the shell layer has a higher glass transition point (Tg) than the binder resin contained in the toner core.
In another exemplified toner containing a toner particle having a core-shell structure, the surface of a toner core is coated with a thin film (shell layer) containing a thermosetting resin. The toner core has a softening point of 40° C. or more and 150° C. or less.
An electrostatic latent image developing toner of the present disclosure includes toner particles each having a toner core containing a binder resin and a shell layer coating a surface of the toner core. The shell layer contains a unit derived from a monomer of a thermosetting resin, and a unit derived from a thermoplastic resin. The thermosetting resin is one or more resins selected from the group of amino resins consisting of a melamine resin, a urea resin, and a glyoxal resin.
An embodiment of the present disclosure will now be described in details. The present disclosure is not limited to the following embodiment at all but can be practiced with changes and modifications appropriately made within the scope of the object of the present disclosure. Incidentally, the description may be appropriately omitted in some cases for avoiding redundant description, which does not limit the gist of the present disclosure.
A toner according to the present embodiment is an electrostatic latent image developing toner. Each of toner particles contained in the toner has a toner core and a shell layer coating the toner core. The toner core contains a binder resin. Besides, the toner core may contain, in the binder resin, a component such as a colorant, a release agent, a charge control agent, or a magnetic powder if necessary. The shell layer is mainly constituted by a resin. The resin constituting the shell layer contains a unit derived from a monomer of a thermosetting resin, and a unit derived from a thermoplastic resin.
The toner may contain the toner particles alone, or may contain a component other than the toner particles. An external additive may be adhered to the surface of the toner particle as occasion demands. The toner may be mixed with a desired carrier, so as to be prepared as a two-component developer. Incidentally, a particle obtained before the treatment with an external additive is sometimes described as a toner mother particle in the following description and the appended claims.
Now, the toner core (the binder resin, the colorant, the release agent, the charge control agent, and the magnetic powder), the shell layer, the external additive, the carrier used when the toner is used as a two-component developer, and a method for producing the toner will be successively described.
[Binder Resin]
In the toner of the present embodiment, the shell layer is formed on the surface of the toner core through a reaction, caused on the surface of the toner core, between the thermoplastic resin and the monomer of the thermosetting resin. Therefore, the binder resin is preferably a resin having, in a molecule, at least one of functional groups of a hydroxyl group, a carboxyl group, and an amino group, and is more preferably a resin having, in a molecule, a hydroxyl group and/or a carboxyl group. A hydroxyl group reacts with and chemically binds to a monomer of a thermosetting resin such as methylol melamine. Accordingly, if the toner is produced by using a binder resin having a hydroxyl group, the shell layer is firmly bound to the toner core in the prepared toner.
If the binder resin has a carboxyl group, the binder resin has an acid value of preferably 3 mgKOH/g or more and 50 mgKOH/g or less, and more preferably 10 mgKOH/g or more and 40 mgKOH/g or less. If the binder resin has a hydroxyl group, the binder resin has a hydroxyl value of preferably 10 mgKOH/g or more and 70 mgKOH/g or less, and more preferably 15 mgKOH/g or more and 50 mgKOH/g or less.
Specific examples of the binder resin include thermoplastic resins such as styrene resins, acrylic resins, styrene acrylic resins, polyethylene resins, polypropylene resins, vinyl chloride resins, polyester resins, polyamide resins, polyurethane resins, polyvinyl alcohol resins, vinyl ether resins, N-vinyl resins, and styrene-butadiene resins. Among these resins, a styrene acrylic resin or a polyester resin is preferably used from the viewpoint of improvement of the dispersibility of a colorant in the toner particles, the chargeability of the toner, and the fixability of the toner on a recording medium. The styrene acrylic resin and the polyester resin will now be described.
The styrene acrylic resin is a copolymer of a styrene monomer and an acrylic monomer. Specific examples of the styrene monomer include styrene, α-methylstyrene, p-hydroxystyrene, m-hydroxystyrene, vinyl toluene, α-chlorostyrene, o-chlorostyrene, m-chlorostyrene, p-chlorostyrene, and p-ethylstyrene. Specific examples of the acrylic monomer include (meth)acrylic acid; (meth)acrylic acid alkyl ester such as methyl(meth)acrylate, ethyl(meth)acrylate, n-propyl(meth)acrylate, iso-propyl(meth)acrylate, n-butyl(meth)acrylate, iso-butyl(meth)acrylate, or 2-ethylhexyl(meth)acrylate; and (meth)acrylic acid hydroxyalkyl ester such as 2-hydroxyethyl(meth)acrylate, 3-hydroxypropyl(meth)acrylate, 2-hydroxypropyl(meth)acrylate, or 4-hydroxypropyl(meth)acrylate.
In preparation of the styrene acrylic resin, a hydroxy group can be introduced into the styrene acrylic resin by using a monomer such as p-hydroxystyrene, m-hydroxystyrene, or hydroxyalkyl(meth)acrylate. By appropriately adjusting the amount of such a monomer having a hydroxyl group to be used, the hydroxyl value of the resultant styrene acrylic resin can be adjusted.
In preparation of the styrene acrylic resin, a carboxyl group can be introduced into the styrene acrylic resin by using (meth)acrylic acid as the monomer. By appropriately adjusting the amount of the (meth)acrylic acid to be used, the acid value of the resultant styrene acrylic resin can be adjusted.
The polyester resin can be obtained by condensation polymerization or co-condensation polymerization of a bivalent, trivalent, or higher valent alcohol and a bivalent, trivalent, or higher valent carboxylic acid. Examples of components used in synthesizing the polyester resin include the following alcohols and carboxylic acids:
Specific examples of a bivalent alcohol used in synthesizing the polyester resin include diols such as ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,4-butanediol, neopentyl glycol, 1,4-butenediol, 1,5-pentanediol, 1,6-hexanediol, 1,4-cyclohexanedimethanol, dipropylene glycol, polyethylene glycol, polypropylene glycol, and polytetramethylene glycol; and bisphenols such as bisphenol A, hydrogenated bisphenol A, polyoxyethylenated bisphenol A, and polyoxypropylene-modified bisphenol A.
Specific examples of a trivalent or higher valent alcohol used in synthesizing the polyester resin include sorbitol, 1,2,3,6-hexanetetrol, 1,4-sorbitan, pentaerythritol, dipentaerythritol, tripentaerythritol, 1,2,4-butanetriol, 1,2,5-pentanetriol, glycerol, diglycerol, 2-methyl propanetriol, 2-methyl-1,2,4-butanetriol, trimethylolethane, trimethylolpropane, and 1,3,5-trihydroxymethylbenzene.
Specific examples of a bivalent carboxylic acid used in synthesizing the polyester resin include maleic acid, fumaric acid, citraconic acid, itaconic acid, glutaconic acid, phthalic acid, isophthalic acid, terephthalic acid, cyclohexane dicarboxylic acid, succinic acid (alkyl succinic acid or alkenyl succinic acid), adipic acid, sebacic acid, azelaic acid, and malonic acid. Besides, specific examples of the alkyl succinic acid and 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, n-dodecenyl succinic acid, isododecyl succinic acid, and isododecenyl succinic acid.
Specific examples of a trivalent or higher valent carboxylic acid used in synthesizing the polyester resin 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-methylene carboxy propane, 1,2,4-cyclohexanetricarboxylic acid, tetra(methylenecarboxyl)methane, 1,2,7,8-octanetetracarboxylic acid, pyromellitic acid, and Empol trimer acid.
Furthermore, any of the aforementioned bivalent, trivalent, or higher valent carboxylic acids may be used in the form of an ester-forming derivative such as an acid halide, an acid anhydride, or a lower alkyl ester. Here, a “lower alkyl” means an alkyl group having 1 to 6 carbon atoms.
The acid value and the hydroxyl value of the polyester resin can be adjusted by appropriately changing the amount of a bivalent, trivalent or higher valent alcohol and the amount of a bivalent, trivalent or higher valent carboxylic acid to be used in producing the polyester resin. Besides, the acid value and the hydroxy value of the polyester resin tend to be lowered by increasing the molecular weight of the polyester resin.
From the viewpoint of carbon neutral, the toner preferably contains a biomass-derived material. Specifically, a ratio of biomass-derived carbon in entire carbon contained in the toner is preferably 25% by mass or more and 90% by mass or less.
As the binder resin, a polyester resin synthesized by using a biomass-derived alcohol, such as 1,2-propanediol, 1,3-propanediol, or glycerin is preferably used.
The type of biomass is not especially limited, and the biomass may be plant biomass or animal biomass. Among various biomass-derived materials, a plant biomass-derived material is more preferably used because such a material is easily available in a large amount and is inexpensive.
An example of a method for producing glycerin from biomass includes a method in which vegetable oil or animal oil is hydrolyzed by a chemical method using an acid or a base, or by a biological method using an enzyme or microorganism. Alternatively, glycerin may be produced from a substrate containing saccharides such as glucose by a fermentation method. Alcohol such as 1,2-propanediol or 1,3-propanediol can be produced by using, as a raw material, the glycerin obtained as described above. The glycerin can be chemically transformed into a target substance by a known method.
As the binder resin, a styrene acrylic resin synthesized by using biomass-derived acrylic acid or acrylate is preferably used. By dehydrating the glycerin obtained as described above, acrolein can be obtained. Besides, by oxidizing the thus obtained acrolein, biomass-derived acrylic acid can be obtained. Furthermore, by esterifying the thus obtained biomass-derived acrylic acid by a known method, biomass-derived acrylate can be produced. If alcohol used in producing acrylate is methanol or ethanol, alcohol produced from biomass by a known method is preferably used.
In CO2 present in the air, the concentration of CO2 containing radioactive carbon (14C) is retained constant in the air. On the other hand, plants incorporate CO2 containing 14C from the air during photosynthesis. Therefore, the concentration of 14C in carbon contained in an organic component of a plant is occasionally equivalent to the concentration of CO2 containing 14C in the air. The concentration of 14C in carbon contained in an organic component of a general plant is approximately 107.5 pMC (percent Modern Carbon). Besides, carbon present in animals is derived from carbon contained in plants. Therefore, the concentration of 14C in carbon contained in an organic component of an animal also shows a similar tendency to that in a plant.
Assuming that the concentration of 14C in the toner is X(pMC), the ratio of biomass-derived carbon in entire carbon contained in the toner can be obtained in accordance with formula (1): Ratio of biomass-derived carbon (mass %)=(X/107.5)×100.
From the viewpoint of the carbon neutral, a plastic product containing biomass-derived carbon in a ratio of 25% by mass or more in entire carbon contained in the product is particularly preferred. Such a plastic product is given a BiomassPla mark (certified by Japan BioPlastics Association). In the case where the ratio of the biomass-derived carbon in entire carbon contained in the toner is 25% by mass or more, the concentration X of 14C in the toner is obtained in accordance with the above formula (1) as 26.9 pMC or more. Accordingly, the polyester resin is preferably prepared so that the concentration of the radioactive carbon isotope 14C in the entire carbon contained in the toner can be 26.9 pMC or more. Incidentally, the concentration of 14C in carbon contained in a petrochemical can be measured in accordance with ASTM-D6866.
The glass transition point (Tgr) of the binder resin is preferably 30° C. or more and 60° C. or less, and more preferably 35° C. or more and 55° C. or less. The glass transition point (Tgr) of the binder resin can be measured by the following method.
<Method for Measuring Glass Transition Point>
The glass transition point (Tgr) of the binder resin can be obtained on the basis of a heat absorption curve of the binder resin (more specifically, a point of change in specific heat of the binder resin) obtained by using a differential scanning calorimeter (DSC) (such as “DSC-6200” manufactured by Seiko Instruments Inc.). For example, 10 mg of the binder resin (measurement sample) is put in an aluminum pan, and an empty aluminum pan is used as a reference. A heat absorption curve of the binder resin is obtained through measurement performed under conditions of a measurement temperature range from 25° C. to 200° C. and a temperature increasing rate of 10° C./min. The glass transition point (Tgr) of the binder resin can be obtained based on this heat absorption curve of the binder resin.
The binder resin has a softening point (Tmr) of preferably 60° C. or more and 150° C. or less, and more preferably 70° C. or more and 140° C. or less. Alternatively, a plurality of resins having different softening points (Tm) can be combined to obtain a binder resin having a softening point (Tmr) falling in the aforementioned range. The softening point (Tmr) of the binder resin can be measured by the following method.
<Method for Measuring Softening Point>
The softening point (Tmr) of the binder resin can be measured by using an elevated flow tester (such as “CFT-500D” manufactured by Shimadzu Corporation). For example, the softening point (Tmr) can be measured by setting the binder resin (measurement sample) on the elevated flow tester and causing 1 cm3 of the sample to be melt flown under conditions of a die diameter of 1 mm, a plunger load of 20 kg/cm2, and a temperature increasing rate of 6° C./min. By the measurement with the elevated flow tester, an S shaped curve pertaining to the temperature (° C.)/stroke (mm) can be obtained. The softening point (Tmr) of the binder resin can be read from the thus obtained S shaped curve.
A method for reading the softening point (Tmr) of the binder resin will be described with reference to
If a polyester resin is used as the binder resin, the polyester resin has a number average molecular weight (Mn) of preferably 1200 or more and 2000 or less. A molecular weight distribution (Mw/Mn) of the polyester resin expressed as a ratio between the number average molecular weight (Mn) and a mass average molecular weight (Mw) of the polyester resin is preferably 9 or more and 20 or less. If a styrene acrylic resin is used as the binder resin, the styrene acrylic resin has a number average molecular weight (Mn) of preferably 2000 or more and 3000 or less. A molecular weight distribution (Mw/Mn) of the styrene acrylic resin expressed as a ratio between the number average molecular weight (Mn) and the mass average molecular weight (Mw) of the styrene acrylic resin is preferably 10 or more and 20 or less. The number average molecular weight (Mn) and the mass average molecular weight (Mw) of the binder resin can be measured by gel permeation chromatography.
[Colorant]
The toner core may contain a colorant if necessary. As the colorant, any of known pigments or dyes can be used in accordance with the color of the toner particles. Specific examples of the colorant suitably used include the following:
An example of a black colorant includes carbon black. Alternatively, a colorant whose color is adjusted to black by using colorants such as a yellow colorant, a magenta colorant, and a cyan colorant described later may be used as the black colorant.
If the toner is a color toner, examples of the colorant mixed in the toner core include a yellow colorant, a magenta colorant, and a cyan colorant.
Examples of the yellow colorant include condensed azo compounds, isoindolinone compounds, anthraquinone compounds, azo metal complexes, methine compounds and allylamide compounds. Specific examples of the yellow colorant include C.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); and Naphthol Yellow S, Hansa Yellow G, and C.I. Bat Yellow.
Examples of the magenta colorant include condensed azo compounds, diketopyrrolopyrrole compounds, anthraquinone compounds, quinacridone compounds, basic dye lake compounds, naphthol compounds, benzimidazolone compounds, thioindigo compounds, and perylene compounds. A specific example of the magenta colorant includes C.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).
Examples of the cyan colorant include copper phthalocyanine compounds, copper phthalocyanine derivatives, anthraquinone compounds, and basic dye lake compounds. Specific examples of the cyan colorant include C.I. Pigment Blue (1, 7, 15, 15:1, 15:2, 15:3, 15:4, 60, 62, or 66); and phthalocyanine blue, C.I. Bat Blue, or C.I. Acid Blue.
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 based on 100 parts by mass of the binder resin.
[Release Agent]
The toner core may contain a release agent if necessary. The release agent is used generally for purpose of improving the fixability or the offset resistance of the toner.
Suitable examples of the release agent include aliphatic hydrocarbon waxes such as low molecular weight polyethylene, low molecular weight polypropylene, polyolefin copolymers, polyolefin wax, microcrystalline wax, paraffin wax, and Fischer-Tropsch wax; oxides of the aliphatic hydrocarbon waxes such as polyethylene oxide wax, and a block copolymer of polyethylene oxide wax; vegetable waxes such as candelilla wax, carnauba wax, haze wax, jojoba wax, and rice wax; animal waxes such as beeswax, lanolin, and spermaceti wax; mineral waxes such as ozokerite, ceresin, and petrolatum; waxes containing a fatty acid ester as a principal component such as montanic acid ester wax, and castor wax; and waxes obtained by deoxidizing part or whole of fatty acid ester such as deoxidized carnauba wax.
The amount of the release agent to be used is preferably 1 part by mass or more and 30 parts by mass or less, and more preferably 5 parts by mass or more and 20 parts by mass or less based on 100 parts by mass of the binder resin.
[Charge Control Agent]
A charge control agent is used for purpose of improving the charge level or the charge rising property of a toner, so as to obtain a toner excellent in the durability or the stability. The charge rising property of a toner is an index whether or not the toner can be charged to prescribed charge level in a short period of time.
If development is performed with the toner positively charged, a positively chargeable charge control agent is preferably used. If the development is performed with the toner negatively charged, a negatively chargeable charge control agent is preferably used. If sufficient chargeability is secured in the toner, however, there is no need to use a charge control agent. For example, if a component having a charging function is contained in the shell layer, there is no need to add a charge control agent to the toner core.
Specific examples of the positively chargeable charge control agent include azine compounds such as pyridazine, pyrimidine, pyrazine, ortho-oxazine, meta-oxazine, para-oxazine, ortho-thiazine, meta-thiazine, para-thiazine, 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, and quinoxaline; direct dyes containing an azine compound such as 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; nigrosine compounds such as nigrosine, nigrosine salts and nigrosine derivatives; acidic dyes containing a nigrosine compound such as nigrosine BK, nigrosine NB, and nigrosine Z; metal salts of naphthenic acid or higher fatty acid; alkoxylated amine; alkyl amide; and quaternary ammonium salts such as benzyldecylhexylmethylammonium chloride and decyl trimethyl ammonium chloride. Among these positively chargeable charge control agents, nigrosine compounds are particularly preferably used because a rapider charge rising property can be attained by them. Two or more of these positively chargeable charge control agents may be used in combination.
A resin having a quaternary ammonium salt, a carboxylate, or a carboxyl group can be used as the positively chargeable charge control agent. Specific examples of such a resin include styrene resins having a quaternary ammonium salt, acrylic resins having a quaternary ammonium salt, styrene acrylic resins having a quaternary ammonium salt, polyester resins having a quaternary ammonium salt, styrene resins having a carboxylate, acrylic resins having a carboxylate, styrene acrylic resins having a carboxylate, polyester resins having a carboxylate, styrene resins having a carboxyl group, acrylic resins having a carboxyl group, styrene acrylic resins having a carboxyl group, and polyester resins having a carboxyl group. Such a resin may be an oligomer or a polymer.
Specific examples of the negatively chargeable charge control agent include organic metal complexes and chelate compounds. As the organic metal complexes and the chelate compounds, acetylacetone metal complexes such as aluminum acetyl acetonate and iron (II) acetyl acetonate, salicylic acid metal complexes and salicylic acid metal salts such as chromium 3,5-di-tert-butylsalicylate are preferably used, and a salicylic acid metal complex or salicylic acid metal salt is more preferably used. Two or more of these negatively chargeable charge control agents may be used in combination.
The amount of the positively chargeable or negatively chargeable charge control agent to be used is preferably 0.5 part by mass or more and 20.0 parts by mass or less, more preferably 1.0 part by mass or more and 15.0 parts by mass or less assuming that the total mass of the toner is 100 parts by mass.
[Magnetic Powder]
The toner core may contain a magnetic powder in the binder resin if necessary. A toner containing toner particles produced by using such a toner core containing a magnetic powder is used as a magnetic one-component developer. Examples of a suitable material of the magnetic powder include iron such as ferrite and magnetite; ferromagnetic metals such as cobalt and nickel; alloys containing iron and/or a ferromagnetic metal; compounds containing iron and/or a ferromagnetic metal; ferromagnetic alloys having been ferromagnetized by heating or the like; and 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. If a magnetic powder having a particle size falling in this range is used, the magnetic powder can be easily homogeneously dispersed in the binder resin.
The amount of the magnetic powder to be used in a toner working as a one-component developer is preferably 35 parts by mass or more and 60 parts by mass or less, and more preferably 40 parts by mass or more and 60 parts by mass or less assuming that the total amount of the toner is 100 parts by mass. Alternatively, the amount of the magnetic powder to be used in a toner working as a two-component developer is preferably 20 parts by mass or less and more preferably 15 parts by mass or less assuming that the total amount of the toner is 100 parts by mass.
[Resin Constituting Shell Layer]
The resin constituting the shell layer contains the unit derived from the monomer of the thermosetting resin and the unit derived from the thermoplastic resin. It is noted that the unit derived from the monomer of the thermosetting resin means, in the present application and the appended claims, a unit obtained by introducing a methylene group (—CH2—) derived from formaldehyde into a monomer such as melamine.
The resin constituting the shell layer is formed through a reaction between the monomer of the thermosetting resin and the thermoplastic resin. The unit derived from the thermoplastic resin is crosslinked by the unit derived from the monomer of the thermosetting resin. Therefore, the shell layer of the toner of the present embodiment has suitable flexibility owing to the unit derived from the thermoplastic resin as well as suitable mechanical strength owing to a three-dimensional crosslinked structure formed by the monomer of the thermosetting resin. Accordingly, the shell layer of the toner of the present embodiment is not easily broken during storage or transportation but is easily broken by applying heat and pressure in fixing the toner. For these reasons, the toner of the present embodiment is excellent in the high-temperature preservability and the low-temperature fixability even if the shell layer is thin. Now, materials suitably used for forming the resin constituting the shell layer (i.e., examples of the monomer of the thermosetting resin, and the thermoplastic resin) will be described.
(Monomer of Thermosetting Resin)
A monomer or prepolymer used for introducing the unit derived from the monomer of the thermosetting resin into the resin constituting the shell layer is a monomer or an initial condensation product used in forming one or more thermosetting resins selected from the group of amino resins consisting of a melamine resin, a urea resin, and a glyoxal resin.
The melamine resin is a polycondensate of melamine and formaldehyde. A monomer used for forming the melamine resin is melamine. The urea resin is a polycondensate of urea and formaldehyde. A monomer used for forming the urea resin is urea. The glyoxal resin is a polycondensate of a reactant between glyoxal and urea, and formaldehyde. A monomer used for forming the glyoxal resin is a reactant between glyoxal and urea. Each of the melamine used for forming the melamine resin, the urea used for forming the urea resin, and the urea to be reacted with glyoxal may be modified by a known method. The monomer of the thermosetting resin may be methylolated (derivatized) by formaldehyde before reacting with the thermoplastic resin.
The shell layer of the toner of the present embodiment contains a nitrogen atom derived from melamine or urea. Therefore, the toner of the present embodiment having the shell layer containing the nitrogen atom can be easily positively charged. Therefore, if the toner of the present embodiment is positively charged to form an image, toner particles contained in the toner can be easily positively charged to have a desired charge amount. In order to positively charge the toner particles contained in the toner to have a desired charge amount, the content of the nitrogen atom in the shell layer is preferably 10% by mass or more.
(Thermoplastic Resin)
The thermoplastic resin used for introducing the unit derived from the thermoplastic resin into the resin constituting the shell layer is preferably a thermoplastic resin having a functional group reactive with a functional group (such as a methylol group or an amino group) of the aforementioned monomer of the thermosetting resin. Examples of the functional group reactive with a methylol group or an amino group include functional groups including an active hydrogen atom such as a hydroxyl group, a carboxyl group, and an amino group. An amino group may be contained in the thermoplastic resin in the form of a carbamoyl group (—CONH2). The thermoplastic resin is preferably a resin containing a unit derived from (meth)acrylamide, or a resin containing a unit derived from a monomer having a functional group such as a carbodiimide group, an oxazoline group, or a glycidyl group because the shell layer can be easily formed when such a resin is used.
Specific examples of the thermoplastic resin used for forming the shell layer include (meth)acrylic resins, styrene-(meth)acrylic copolymer resins, silicone-(meth)acrylic graft copolymers, polyurethane resins, polyester resins, polyvinyl alcohols, and ethylene vinyl alcohol copolymers. Such resins may contain a unit derived from a monomer having a functional group such as a carbodiimide group, an oxazoline group, or a glycidyl group. Among these resins, the thermoplastic resin is preferably a (meth)acrylic resin, a styrene-(meth)acrylic copolymer resin, or a silicone-(meth)acrylic graft copolymer, and is more preferably a (meth)acrylic resin.
Examples of a (meth)acrylic monomer usable for preparing the (meth)acrylic resins include (meth)acrylic acid; alkyl ester(meth)acrylate such as methyl(meth)acrylate, ethyl(meth)acrylate, n-propyl(meth)acrylate, or n-butyl(meth)acrylate; aryl ester(meth)acrylate such as phenyl(meth)acrylate; hydroxyalkyl ester(meth)acrylate such as 2-hydroxyethyl(meth)acrylate, 3-hydroxypropyl(meth)acrylate, 2-hydroxypropyl(meth)acrylate, or 4-hydroxybutyl(meth)acrylate; (meth)acrylamide; an ethylene oxide adduct of (meth)acrylic acid; alkyl ether, such as methyl ether, ethyl ether, n-propyl ether, or n-butyl ether, of an ethylene oxide adduct of (meth)acrylic ester.
The shell layer is formed preferably in an aqueous medium. Thus, elution of a release agent component contained in the toner core, or dissolution of the binder resin can be suppressed. The thermoplastic resin used for forming the shell layer is preferably water-soluble. Besides, the thermoplastic resin used for forming the shell layer is preferably a resin that can chemically bind to both of the monomer of the thermosetting resin and the toner core in an aqueous medium. An aqueous solution of the thermoplastic resin is preferably used for forming the shell layer.
A ratio (Ws/Wp), in the resin constituting the shell layer, of a content (Ws) of the unit derived from the monomer of the thermosetting resin to a content (Wp) of the unit derived from the thermoplastic resin is preferably 3/7 or more and 8/2 or less, and more preferably 4/6 or more and 7/3 or less.
The thickness of the shell layer is preferably 1 nm or more and 20 nm or less, and more preferably 1 nm or more and 10 nm or less. If an image is formed by using a toner containing toner particles having a too thick shell layer, the shell layer is difficult to break in fixing the toner onto a recording medium even if a pressure is applied to the toner particles. Furthermore, the binder resin and the release agent contained in the toner core are not rapidly softened and molten, and hence, the toner is difficult to fix on a recording medium in a low temperature region. On the other hand, if the shell layer is too thin, the strength of the shell layer is low. If the strength of the shell layer is low, the shell layer may be broken by impact caused in a situation of transportation or the like. Besides, if the toner is stored at a high temperature, toner particles having a shell layer at least partly broken are easily aggregated. This is because a component of the release agent or the like can easily exude onto the surface of the toner particle through a broken portion of the shell layer.
The thickness of the shell layer can be measured by analyzing a TEM image of the cross-section of the toner particle by using commercially available image analysis software. As the commercially available image analysis software, for example, WinROOF (manufactured by Mitani Corporation) can be used. Specifically, two straight lines are drawn to cross at substantially the center of the cross-section of a toner particle, and the lengths of four sections of the two straight lines crossing the shell layer are measured. An average of the thus measured lengths of the four sections is defined as the thickness of the shell layer of one toner particle to be measured. This measurement of the thickness of the shell layer is performed on ten or more toner particles, so as to obtain an average of the thicknesses of the shell layers of the plural toner particles to be measured. The thus obtained average is determined as the thickness of the shell layer of the toner particles.
If the shell layer is too thin, it may be difficult to measure the thickness of the shell layer because the interface between the shell layer and the toner core is unclear on a TEM image. In such a case, with a TEM image combined with energy dispersive X-ray spectroscopic analysis (EDX), mapping of an element characteristic to the material of the shell layer (such as nitrogen) is performed on the TEM image, so as to clear the interface between the shell layer and the toner core, and then, the thickness of the shell layer is measured.
The thickness of the shell layer may be adjusted by adjusting the amounts of the materials to be used for forming the shell layer (such as the monomer of the thermosetting resin, and the thermoplastic resin). The thickness of the shell layer can be presumed, for example, based on the specific surface area of the toner core, the amount of the monomer of the thermosetting resin and the amount of the thermoplastic resin in accordance with the following formula:
Thickness of shell layer=(amount of monomer of thermosetting resin+amount of thermoplastic resin)/specific surface area of toner core
[External Additive]
In the toner of the present embodiment, an external additive may be adhered to the surface of the shell layer as occasion demands.
Examples of the external additive include silica and a metal oxide (such as aluminum, titanium oxide, magnesium oxide, zinc oxide, strontium titanate, or barium titanate).
The external additive has a particle size of preferably 0.01 μm or more and 1.0 μm or less.
The amount of the external additive to be used is preferably 1 part by mass or more and 10 parts by mass or less, and more preferably 2 parts by mass or more and 5 parts by mass or less based on 100 parts by mass of toner mother particles.
[Carrier]
The toner can be mixed with a desired carrier to be used as a two-component developer. In preparing a two-component developer, a magnetic carrier is preferably used.
An example of a suitable carrier includes one obtained by coating a carrier core with a resin. Specific examples of the carrier core include a particle of a material such as iron, oxidized iron, reduced iron, magnetite, copper, silicon steel, ferrite, nickel, or cobalt; a particle of an alloy of such a material and manganese, zinc, or aluminum; a particle of an iron-nickel alloy or an iron-cobalt alloy; a particle of a ceramic such as titanium oxide, aluminum oxide, copper oxide, magnesium oxide, lead oxide, zirconium oxide, silicon carbide, magnesium titanate, barium titanate, lithium titanate, lead titanate, lead zirconate, or lithium niobate; and a particle of a high-dielectric constant material such as ammonium dihydrogen phosphate, potassium dihydrogen phosphate, or Rochelle salt. A resin carrier containing any of these particles (magnetic particles) dispersed in a resin may be used as a carrier.
Specific examples of the resin coating the carrier core include (meth)acrylic polymers, styrene polymers, styrene-(meth)acrylic copolymers, olefin polymers (such as polyethylene, chlorinated polyethylene, and polypropylene), polyvinyl chloride, polyvinyl acetate, polycarbonate, cellulose resins, polyester resins, unsaturated polyester resins, polyamide resins, polyurethane resins, epoxy resins, silicone resins, fluorine resins (such as polytetrafluoroethylene, polychlorotrifluoroethylene, or polyvinylidene fluoride), phenol resins, xylene resins, diallyl phthalate resins, polyacetal resins, and amino resins. Two or more of these resins may be used in combination.
The carrier has a particle size, measured by using an electron microscope, of preferably 20 μm or more and 120 μm or less, and more preferably 25 μm or more and 80 μm or less.
If the toner is used as a two-component developer, the content of the toner in the two-component developer is preferably 3% by mass or more and 20% by mass or less, and more preferably 5% by mass or more and 15% by mass or less based on the mass of the two-component developer.
As a method for producing the toner, a method in which the toner core can be coated with the shell layer of any of the aforementioned prescribed materials is preferably employed. Now, a method for producing the toner core and a method for forming the shell layer employed in a suitable method for producing the electrostatic latent image developing toner of the present embodiment will be successively described.
[Method for Producing Toner Core]
As a method for producing the toner core, a method in which the components such as a colorant, a charge control agent, a release agent, and a magnetic powder can be satisfactorily dispersed in the binder resin is preferably employed.
A zeta potential of the toner core measured in an aqueous medium adjusted to pH 4 (more specifically, a zeta potential measured by a method described later) is preferably negative (namely, lower than 0 mV). A frictional charge amount of the toner core measured by using a standard carrier (more specifically, a frictional charge amount measured by a method described later) is preferably negative (namely, lower than 0 μC/g). If the toner core having such characteristics is used, the shell layer can be easily formed uniformly on the surface of the toner core.
More specifically, if a shell layer is formed on the surface of a toner core in an aqueous medium, there is a tendency that a uniform shell layer cannot be formed on the surface of a toner core unless toner cores are highly dispersed in the aqueous medium containing a dispersant. If at least one of the zeta potential and the frictional charge amount of the toner core is negative as described above, however, the monomer of the thermosetting resin, which is a nitrogen-containing compound and is positively charged in an aqueous medium, is probably electrically drawn to the toner core negatively charged in the aqueous medium. Besides, there is a tendency that a reaction between the monomer of the thermosetting resin having been adsorbed onto the toner core and the thermoplastic resin is satisfactorily proceeded on the surface of the toner core. Since the reaction is satisfactorily proceeded on the surface of the toner core, the shell layer can be easily formed uniformly on the surface of the toner core even if the toner cores are not highly dispersed in the aqueous medium by using a dispersant.
If the toner core showing negative polarity in at least one of the zeta potential and the frictional charge amount is used, it seems as described above that a toner particle containing a toner core coated with a uniform shell layer can be easily obtained without using a dispersant. Besides, if the toner is produced without using a dispersant, which causes extremely high drainage load, the concentration of total organic carbon in a drainage can be probably suppressed to a low level (of, for example, 15 mg/L or less).
<Method for Measuring Zeta Potential in Dispersion of pH 4>
Zero point two (0.2) g of toner core, 80 g of ion-exchanged water, and 20 g of 1 mass % nonionic surfactant (“K-85” manufactured by Nippon Shokubai Co., Ltd., polyvinylpyrrolidone) are mixed by using a magnetic stirrer, so as to homogeneously disperse the toner cores in the resulting liquid. Thus, a dispersion is obtained. Thereafter, dilute hydrochloric acid is added to the dispersion to adjust the pH of the dispersion to 4, and thus, a toner core dispersion of pH 4 (measurement sample) is obtained. The zeta potential of the toner core in the measurement sample is measured by using a zeta potential and particle size analyzer (“Delsa Nano HC” manufactured by Beckman Coulter).
<Method for Measuring Frictional Charge Amount>
One hundred (100) parts by mass of a standard carrier N-01 (a standard carrier for a negatively chargeable toner) available from The Imaging Society of Japan, and 7 parts by mass of the toner core are mixed by using a Turbula mixer for 30 minutes. After mixing, the frictional charge amount of the toner core is measured by using a QM meter (“MODEL 210HS-2A” manufactured by TREK Inc.). The frictional charge amount of the toner core thus measured is used as an index for determining how easily the toner core can be charged (or which polarity the toner core can be easily charged to).
Examples of the method for producing the toner core include a melt kneading method (pulverization method) and an aggregation method. Toner core can be produced more easily by the melt kneading method than by the aggregation method. Toner core with high sphericity can be more easily produced by the aggregation method than by the melt kneading method. Toner core having uniform shape and particle size can be more easily produced by the aggregation method.
<Melt Kneading Method (Pulverization Method)>
The melt kneading method (pulverization method) includes: kneading materials contained in a toner particle or a toner core; pulverizing the resulting kneaded product; and classifying the resulting pulverized product. In the melt kneading method, a binder resin and an internal additive to be added if necessary (namely, an arbitrary component such as a colorant, a release agent, a charge control agent, or a magnetic powder) are mixed. Subsequently, the resulting mixture is melt kneaded. Thereafter, the resulting melt kneaded product is pulverized and classified. Thus, a toner core having a desired particle size can be obtained.
The glass transition point Tgc of the toner core can be adjusted by adjusting the glass transition point Tgr of a binder resin contained in the toner core. If a binder resin having a high glass transition point Tgr is used, a toner core having a high glass transition point Tgc can be obtained. Alternatively, the glass transition point Tgc of the toner core can be adjusted by adjusting the type or amount of a release agent contained in the toner core. If a toner core is produced by using a release agent having a low melting point, or by using a large amount of release agent, there is a tendency that toner particles having a low glass transition point Tgc are obtained. The glass transition point Tgc of the toner core can be measured by a method similar to that employed for measuring the glass transition point Tgr of a binder resin.
<Aggregation Method>
The aggregation method preferably includes an aggregation process and a coalescence process described below. In the aggregation process, fine particles containing components of the toner core are aggregated in an aqueous medium to form aggregated particles. In the coalescence process, components contained in the aggregated particles are coalesced in an aqueous medium to form a toner core.
[Aggregation Process]
In the aggregation process, fine particles containing components of the toner core (hereinafter referred to as the core fine particles) are used. The core fine particles may contain, in addition to the binder resin described above, a component such as a colorant, a release agent, or a charge control agent.
An aqueous dispersion containing the core fine particles can be prepared, for example, by micronizing a binder resin (or a composition containing a binder resin) to a desired size in an aqueous medium. The aqueous dispersion containing the core fine particles may contain other fine particles apart from the fine particles containing the binder resin. Examples of the other fine particles apart from the fine particles containing the binder resin include fine particles of a colorant, fine particles of a release agent, and fine particles containing a colorant and a release agent. Now, a method for preparing the fine particles containing a binder resin, a method for preparing the fine particles of a colorant, and a method for preparing the fine particles of a release agent will be successively described.
(Method for Preparing Fine Particles Containing Binder Resin)
A suitable example of the method for preparing fine particles containing a binder resin will now be described.
A resin composition containing a binder resin and an internal additive (arbitrary component) added if necessary is primarily pulverized by using a pulverizer such as a turbo mill. The resulting primarily pulverized product is dispersed in an aqueous medium such as ion-exchanged water, and in this state, it is heated to a temperature higher, by 10° C. or more (Tmr+10° C.) and 20° C. or less, than the softening point (Tmr) of the binder resin measured by using a flow tester. Subsequently, to the thus heated dispersion of the binder resin, a strong shearing force is applied by using a high-speed shearing emulsifier such as Clearmix (manufactured by M Technique Co., Ltd.). In this manner, an aqueous dispersion including fine particles containing the binder resin (hereinafter referred to as the resin dispersion) is obtained.
The volume average particle size (D50) of the fine particles containing the binder resin is preferably 1 μm or less, and more preferably 0.05 μm or more and 0.5 μm or less. If the fine particles containing the binder resin have a particle size (D50) of 1 μm or less, toner cores having a sharp particle size distribution and having a uniform shape can be easily obtained. The volume average particle size (D50) of the fine particles containing the binder resin can be measured by using, for example, a laser diffraction particle size analyzer (such as “SALD-2200” (manufactured by Shimadzu Corporation)).
The resin dispersion preferably contains a surfactant. If the resin dispersion contains a surfactant, the fine particles containing the binder resin can be easily stably dispersed in the aqueous medium.
The surfactant that may be contained in the resin dispersion can be appropriately selected from the group consisting of an anionic surfactant, a cationic surfactant, and a nonionic surfactant. Examples of the anionic surfactant include a sulfuric acid ester salt type surfactant, a sulfonic acid salt type surfactant, a phosphoric acid ester salt type surfactant, and soap. Examples of the cationic surfactant include an amine salt type surfactant and a quaternary ammonium salt type surfactant. Examples of the nonionic surfactant include a polyethylene glycol type surfactant, an alkylphenol ethylene oxide adduct type surfactant, and a polyvalent alcohol type surfactant containing a derivative of a polyvalent alcohol (such as glycerin, sorbitol, or sorbitan). Among these surfactants, an anionic surfactant is preferably used. One of the aforementioned surfactants may be singly used, or two or more of these may be used in combination.
The amount of the surfactant to be used is preferably 0.01% by mass or more and 10% by mass or less based on the mass of the binder resin.
In using a resin having an acidic group as the binder resin, if the binder resin is directly micronized in an aqueous medium, the specific surface area of the binder resin may be so increased that the pH of the aqueous medium may be lowered to approximately 3 to 4 due to the influence of the acidic group exposed on the surface of the fine particles containing the binder resin. In the aqueous medium having pH of approximately 3 to 4, the binder resin may be hydrolyzed, or the fine particles containing the binder resin cannot be micronized to a desired particle size.
In order to suppress the aforementioned problem derived from the acidic group, a basic substance may be added to the aqueous medium in preparing the fine particles containing the binder resin. Examples of the basic substance include alkali metal hydroxide such as sodium hydroxide, potassium hydroxide, or lithium hydroxide; alkali metal carbonate such as sodium carbonate or potassium carbonate; alkali metal hydrogencarbonate such as sodium hydrogencarbonate or potassium hydrogencarbonate; and a nitrogen-containing organic base such as N,N-dimethylethanolamine, N,N-diethylethanolamine, triethanolamine, tripropanolamine, tributanolamine, triethylamine, n-propylamine, n-butylamine, isopropylamine, monomethanolamine, morpholine, methoxypropylamine, pyridine, or vinylpyridine.
(Method for Preparing Fine Particles of Release Agent)
A suitable example of the method for preparing fine particles of a release agent will now be described.
A release agent is precedently pulverized into a size of approximately 100 μm or less to obtain a powder of the release agent. For preparing the fine particles of the release agent, a slurry is preferably prepared by adding the powder of the release agent to an aqueous medium containing a surfactant. The amount of the surfactant to be used is preferably 0.01% by mass or more and 10% by mass or less based on the mass of the release agent.
Next, the thus obtained slurry is heated to a temperature beyond the melting point of the release agent. Subsequently, a strong shearing force is applied to the heated slurry by using a homogenizer (“Ultra-Turrax T50” manufactured by IKA) or a pressure-ejecting type disperser, so as to prepare an aqueous medium containing release agent fine particles (hereinafter referred to as the release dispersion). An apparatus for applying a strong shearing force to the dispersion is, for example, NANO3000 (manufactured by Beryu Co., Ltd.), Nanomizer (manufactured by Yoshida Kikai Co., Ltd.), Microfluidizer (manufactured by MFI), Gaulin Homogenizer (manufactured by Manton Gaulin), or Clearmix W Motion (manufactured by M Technique Co., Ltd.).
The volume average particle size (D50) of the fine particles of the release agent contained in the release dispersion is preferably 1 μm or less, more preferably 0.1 μm or more and 0.7 μm or less, and particularly preferably 0.28 μm or more and 0.55 μm or less. If fine particles of the release agent having a particle size (D50) of 1 μm or less are used, a toner particle in which the release agent is homogeneously dispersed in the binder resin can be easily obtained. The volume average particle size (D50) of the fine particles of the release agent can be measured by a similar method to the measurement method for the volume average particle size (D50) of the fine particles containing the binder resin.
(Method for Preparing Fine Particles of Colorant)
A suitable example of the method for preparing fine particles of a colorant will now be described.
An aqueous dispersion containing fine particles of a colorant (hereinafter referred to as the coloring dispersion) is preferably prepared by dispersing, by using a known disperser, the colorant and a dispersant for the colorant added if necessary (an arbitrary component) in an aqueous medium containing a surfactant. As the surfactant, the same surfactant as that used in preparing the fine particles containing the binder resin can be used. The amount of the surfactant to be used is preferably 0.1% by mass or more and 10% by mass or less based on the mass of the colorant.
The disperser used for the dispersion of the colorant is not especially limited, and for example, a pressure disperser such as an ultrasonic disperser, a mechanical homogenizer, Manton Gaulin, a pressure homogenizer, or a high-pressure homogenizer (manufactured by Yoshida Kikai Co., Ltd.); or a medium type disperser such as a sand grinder, a horizontal hand mill, a vertical bead mill, Ultra Apex Mill (manufactured by Kotobuki Industries Co., Ltd.), Dyno Mill (manufactured by WAB Company), or MSC mill (manufactured by Nippon Coke and Engineering Co., Ltd.) can be used.
The volume average particle size (D50) of the fine particles of the colorant is preferably 0.01 μm or more and 0.2 μm or less. The volume average particle size (D50) of the fine particles of the colorant can be measured by a method similar to the measurement method employed for the volume average particle size (D50) of the fine particles containing the binder resin.
(Formation of Aggregated Particles)
The resin dispersion prepared by the aforementioned method is combined with the release dispersion and/or the coloring dispersion as occasion demands (for example, so that desired components of the toner core can be contained), and thereafter, the fine particles are aggregated, and thus, an aqueous medium including aggregated particles containing the binder resin (hereinafter referred to as the aggregation dispersion) can be obtained.
As a suitable method for aggregating the fine particles, an aggregating agent is added to the resin dispersion after adjusting the pH of the resin dispersion, and then, the temperature of the resin dispersion is adjusted to a prescribed temperature for aggregating the fine particles.
Suitable examples of the aggregating agent include an inorganic metal salt, an inorganic ammonium salt, and a bivalent or higher valent metal complex. Examples of the inorganic metal salt include a metal salt such as sodium sulfate, sodium chloride, calcium chloride, calcium nitrate, barium chloride, magnesium chloride, zinc chloride, aluminum chloride, or aluminum sulfate; and an inorganic metal salt polymer such as polyaluminum chloride or polyaluminum hydroxide. Examples of the inorganic aluminum salt include ammonium sulfate, ammonium chloride, and ammonium nitrate. Alternatively, a quaternary ammonium salt type cationic surfactant, or a nitrogen-containing compound such as polyethyleneimine can be used as the aggregating agent.
Among these aggregating agents, a bivalent metal salt, or a monovalent metal salt is preferably used. One of these aggregating agents may be singly used, or two or more of them may be used in combination. If two or more of the aggregating agents are used in combination, a bivalent metal salt and a monovalent metal salt are preferably used together. A bivalent metal salt and a monovalent metal salt are different in the speed of aggregating fine particles. Therefore, when they are used together, a particle size distribution of the aggregated particles can be easily made sharp while suppressing increase of the particle size of the resulting aggregated particles.
The aggregating agent is added preferably after adjusting the pH of the dispersion of the fine particles. The aqueous dispersion has pH of preferably 8 or more in adding the aggregating agent. The aggregating agent may be added at one time or gradually added.
The amount of the aggregating agent to be added is preferably 1 part by mass or more and 50 parts by mass or less based on 100 parts by mass of a solid content of the aqueous dispersion. The amount of the aggregating agent to be added can be appropriately adjusted in accordance with the type and the amount of anionic or nonionic dispersant contained in the dispersion of the fine particles.
The temperature of the aqueous dispersion at which the fine particles are aggregated is preferably equal to or higher than the glass transition point (Tg) of the binder resin and lower than a temperature beyond the glass transition point (Tg) of the binder resin by 10° C. When the aqueous dispersion containing the fine particles of the binder resin is heated to such a temperature, the aggregation of the fine particles contained in the aqueous dispersion can be satisfactorily proceeded.
After the aggregation is proceeded until the aggregated particles attain a desired particle size, an aggregation terminator may be added. Examples of the aggregation terminator include sodium chloride, potassium chloride, and magnesium chloride.
[Coalescence Process]
In the coalescence process, the aggregation dispersion obtained as described above is heated to coalesce the components contained in the aggregated particles. In this manner, an aqueous dispersion containing a toner core having a desired particle size can be obtained. The temperature to which the aggregation dispersion is heated is preferably equal to or higher than a temperature of the glass transition point (Tg) of the binder resin by 10° C., and equal to or lower than the melting point of the binder resin. When the aggregation dispersion is heated to such a temperature, the coalescence of the components contained in the aggregated particles can be satisfactorily proceeded.
[Washing Process for Toner Core]
In a washing process, the toner core obtained as described above is washed with water. As an exemplified washing method, toner cores are collected as a wet cake by solid-liquid separating the toner cores from the toner core aqueous dispersion, and the resulting wet cake is washed with water. Alternatively, the toner cores contained in the toner core aqueous dispersion are precipitated, the supernatant is exchanged with water, and the toner cores are dispersed again in water after the exchange.
[Drying Process for Toner Core]
As a suitable method for drying the toner core, a dryer such as a spray dryer, a fluidized-bed dryer, a vacuum freeze dryer, or a vacuum dryer is used.
[Method for Forming Shell Layer]
The shell layer coating the toner core can be formed by causing a reaction between the monomer of the thermosetting resin (melamine, urea, or a reactant between glyoxal and urea) and the thermoplastic resin. Alternatively, instead of the monomer of the thermosetting resin, a precursor (a methylolated product) generated through an addition reaction of the monomer of the thermosetting resin and formaldehyde may be used. Incidentally, in order to prevent dissolution of the binder resin or exudation of the release agent contained in the toner core into a solvent used for forming the shell layer, the shell layer is preferably formed in an aqueous medium such as water.
The shell layer is formed preferably by adding materials for forming the shell layer to the aqueous dispersion containing the toner core. Examples of a method for satisfactorily dispersing toner cores in an aqueous medium include a method in which the toner cores are mechanically dispersed in the aqueous medium by using an apparatus capable of powerfully stirring a dispersion (hereinafter referred to as the first dispersion method), and a method in which the toner cores are dispersed in the aqueous medium containing a dispersant (hereinafter referred to as the second dispersion method). In the second dispersion method, the toner cores are readily dispersed in the aqueous medium in a homogeneous manner. Therefore, a uniform shell layer can be easily formed by the second dispersion method. On the other hand, total organic carbon in a drainage can be reduced in the first dispersion method. A suitable example of the stirrer used in the first dispersion method includes HIVIS MIX (manufactured by Primix Corporation).
Suitable examples of the dispersant used in the second dispersion method include compounds such as sodium polyacrylate, poly(paravinylphenol), partially saponified polyvinyl acetate, isoprene sulfonic acid, polyether, an isobutylene/maleic anhydride copolymer, sodium polyaspartate, starch, gelatin, acacia gum, polyvinyl pyrrolidone, and sodium lignosulfonate. One of these dispersants may be singly used, or two or more of them may be used in combination.
The amount of the dispersant to be used is preferably 75 parts by mass or less based on 100 parts by mass of the toner core.
In the second dispersion method using a dispersant, the toner cores are highly dispersed in the medium used for forming the shell layer as described above. Therefore, the toner core particle can be easily uniformly coated by the shell layer. On the contrary, since the toner cores are dispersed by using the dispersant, the dispersant may be adhered to the surface of the toner core before forming the shell layer thereon. If the shell layer is formed with the dispersant present on the interface between the toner core and the shell layer, the adhesion of the shell layer to the toner core is weakened, and hence, there is a tendency that the shell layer is likely to be peeled off from the toner core by mechanical stress applied to the toner. Besides, if the dispersant remains in the toner particles, the dispersant may inhibit the charging of the toner particles in some cases.
The pH of the aqueous dispersion containing the toner core is preferably adjusted to approximately 4 by using an acidic substance before forming the shell layer. By adjusting the pH of the dispersion to be on the acidic side, condensation polymerization of the materials used for forming the shell layer described later can be accelerated.
After adjusting the pH of the aqueous dispersion containing the toner core, the materials used for forming the shell layer may be dissolved in the aqueous dispersion containing the toner core as occasion demands. Thereafter, the reaction between the materials for forming the shell layer is proceeded on the surface of the toner core in the aqueous dispersion, so that the shell layer coating the surface of the toner core can be formed.
The temperature at which the shell layer is formed by causing the reaction between the monomer of the thermosetting resin and the thermoplastic resin is preferably 40° C. or more and 95° C. or less, and more preferably 50° C. or more and 80° C. or less. If the shell layer is formed at a temperature of 40° C. or more and 95° C. or less, the formation of the shell layer can be satisfactorily proceeded.
In the case where the binder resin contains a resin having a hydroxyl group or a carboxyl group (such as a polyester resin), if the shell layer is formed at a temperature of 40° C. or more and 95° C. or less, there is a tendency that the hydroxyl group or the carboxyl group exposed on the surface of the toner core is reacted with the methylol group of the monomer of the thermosetting resin to form a covalent bond between the binder resin contained in the toner core and the resin contained in the shell layer. As a result, the shell layer is easily firmly adhered to the toner core.
After forming the shell layer as described above, the aqueous dispersion containing the toner core coated with the shell layer is cooled to room temperature, and thus, a dispersion of toner mother particles can be obtained. Thereafter, a washing process for washing the toner mother particles, a drying process for drying the toner mother particles, and an external addition process for adhering an external additive to the surfaces of the toner mother particles are successively performed, and then, a toner is collected from the dispersion of the toner mother particles. The washing process, the drying process, and the external addition process will now be described. It is noted that any of the washing process, the drying process, and the external addition process may be appropriately omitted.
[Washing Process for Toner Mother Particles]
The toner mother particles are washed with water if necessary. As a suitable example of a method for washing the toner mother particles, the toner mother particles are collected as a wet cake by solid-liquid separating the toner mother particles from the aqueous medium containing the toner mother particles by a centrifugal separation method or a filter press method, and the obtained wet cake is washed with water. As another suitable example of the method for washing the toner mother particles, the toner mother particles are precipitated in the dispersion containing the toner mother particles, the supernatant is exchanged with water, and the toner mother particles are dispersed again in water after the exchange.
[Drying Process for Toner Mother Particles]
The toner mother particles may be dried if necessary. As a suitable method for drying the toner mother particles, a dryer such as a spray dryer, a fluidized-bed dryer, a vacuum freeze dryer, or a vacuum dryer is used. A spray dryer is more preferably used for suppressing the aggregation of the toner mother particles during the drying process. If a spray dryer is used, an external additive such as silica may be adhered to the surfaces of the toner mother particles by spraying, together with the dispersion of the toner mother particles, a dispersion of the external additive.
[External Addition Process]
An external additive may be adhered to the surfaces of the toner mother particles obtained as described above if necessary. As a suitable example of a method for adhering an external additive to the surfaces of the toner mother particles, the toner mother particles and the external additive are mixed by using a mixer such as a Henschel mixer or a Nauta mixer under conditions where the external additive is not buried in a surface portion of the toner mother particle. By adhering the external additive to the surfaces of the toner mother particles, the toner particles are obtained. Incidentally, if no external additive is adhered to the surfaces of the toner mother particles (namely, the external addition process is omitted), the toner mother particles correspond to the toner particles.
The electrostatic latent image developing toner of the present embodiment described so far is excellent in the high-temperature preservability and the low-temperature fixability. Therefore, the electrostatic latent image developing toner of the present embodiment can be suitably used in any of various image forming apparatuses.
Now, examples of the present disclosure will be described. It is noted that the present disclosure is not limited to the scope of the following examples at all.
(Production of 1,2-propanediol)
A vegetable oil was hydrolyzed to give glycerin. Specifically, a 10 mass % sodium hydroxide aqueous solution in an amount twice as much as that necessary for completely saponifying the vegetable oil was added to the vegetable oil, and the resultant was heated to completely saponify the vegetable oil. After separating an aqueous solution of glycerin from the reaction solution resulting from the saponification, the aqueous solution of glycerin was distilled. Subsequently, the distilled glycerin was treated with active carbon. Thus, purified glycerin was obtained.
The glycerin obtained as described above was used to produce 1,2-propanediol by a method described below.
First, a reactor equipped with a reflux condenser was charged with 200 g of ethylene glycol, and 76 g of copper (II) nitrate trihydrate, and while stirring the contents of the reactor, the temperature was increased to 80° C. and retained at 80° C. for 2 hours. Subsequently, while stirring the contents of the reactor, 52 g of tetraethoxysilane was added dropwise to the reactor, and the resultant was retained at 80° C. for 2 hours. Thereafter, while stirring the contents of the reactor, 18 g of water was added dropwise to the reactor, and the resultant was retained at 80° C. for 3 hours. In this manner, a precipitate was obtained in the reactor.
Subsequently, the thus produced precipitate was dried at approximately 120° C. The thus dried precipitate was fired in the air at 400° C. for 2 hours. Thus, a copper/silica catalyst (having a copper content of 50% by mass) was obtained. Subsequently, an aqueous solution of 29.8 mg of tetraammineplatinum (II) nitrate [Pt(NH3)4(NO3)2] was added to 3 g of the thus obtained copper/silica catalyst, and the resulting liquid was evaporated and dried by using a rotary evaporator. Then, the thus obtained solid was dried at 120° C. Subsequently, the dried solid was fired in the air at 400° C. for 2 hours. In this manner, a copper-platinum/silica catalyst (Cu/Pt/Si=50/0.5/17) (having a copper content of 50% by mass) was obtained.
Subsequently, a 500 mL iron autoclave equipped with a stirrer was charged with 2 g of the copper-platinum/silica catalyst and 200 g of the glycerin. Thereafter, hydrogen was introduced into the autoclave set at 230° C. at a flow rate of 5 L/min (25° C., H2), and with the pressure within the autoclave adjusted to 2 MPa, the contents of the autoclave were reacted for 7 hours. In this manner, a reaction solution was obtained. Thereafter, the reaction solution was purified by a conventional method. In this manner, 1,2-propanediol was obtained.
Polyester resins a to c and a styrene acrylic resin a each having a glass transition point (Tgr), a softening point (Tmr), a number average molecular weight (Mn), a mass average molecular weight (Mw), a molecular weight distribution (Mw/Mn), an acid value, and a hydroxyl value shown in Table 1 below were produced by methods described below. The glass transition points (Tgr) of these binder resins were measured by the aforementioned method.
(Production of Polyester Resin a)
A 5 L four-necked flask was charged with 1245 g of terephthalic acid, 1245 g of isophthalic acid, 1248 g of bisphenol A ethylene oxide adduct, and 744 g of ethylene glycol. Subsequently, after replacing the atmosphere inside the flask with nitrogen, the temperature within the flask was increased to 250° C. under stirring. Then, after the reaction was performed at normal pressure and 250° C. for 4 hours, 0.875 g of antimony trioxide, 0.548 g of triphenyl phosphate, and 0.102 g of tetrabutyl titanate were added to the flask. Thereafter, the pressure within the flask was reduced to 0.3 mmHg, and the temperature within the flask was increased to 280° C. Subsequently, the reaction was performed at 280° C. for 6 hours to give a polyester resin. Then, 30.0 g of trimellitic acid was added as a crosslinking agent to the flask, the pressure within the flask was restored to normal pressure, and the temperature within the flask was lowered to 270° C. Thereafter, the contents within the flask were reacted at normal pressure and 270° C. for 1 hour. After completing the reaction, the content of the flask was taken out and cooled, thereby giving the polyester resin a.
(Production of Polyester Resin b)
The polyester resin b was obtained in the same manner as in the production of the polyester resin a except that 1248 g of bisphenol A ethylene oxide adduct was replaced with 1248 g of bisphenol A propylene oxide adduct.
(Production of Polyester Resin c)
A 5 L four-necked flask equipped with a nitrogen introducing tube, a dehydrating tube, a rectification column, a stirrer, and a thermocouple was charged with 1142 g of the 1,2-propanediol obtained in Production Example 1, 1743 g of terephthalic acid, and 0.5 g of tin (II) octoate used as an esterification catalyst. The contents of the flask were heated to 230° C. under a nitrogen atmosphere. After stirring the contents of the flask at 230° C. for 15 hours, the pressure within the flask was reduced to 8.0 kPa. After the pressure reduction, the content of the flask was stirred at 230° C. for 1 hour. Thereafter, the temperature of the content of the flask was lowered to 180° C., and 288 g of trimellitic anhydride was added to the flask at 180° C. After increasing the temperature of the contents of the flask to 210° C. over 3 hours, the contents of the flask were reacted at 210° C. and atmospheric pressure for 10 hours. After reducing the pressure within the flask to 20 kPa, the polymerization reaction was continued at 210° C. until a polyester resin produced in the flask attained a desired softening point. Then, the polymerization reaction was terminated, and the content of the flask, that is, the polyester resin c, was collected.
(Production of Styrene Acrylic Resin a)
A dispersant aqueous solution was prepared by adding, to a reactor vessel, 200 parts by mass of ion-exchanged water and 0.2 part by mass of polyvinyl alcohol (“PVA235” manufactured by Kuraray Co., Ltd.) used as a dispersant. Subsequently, 100 parts by mass of a monomer component having a monomer composition described below and 3 parts by mass of benzoyl peroxide used as a polymerization initiator were added to the dispersant aqueous solution to give a dispersion.
Then, the temperature of the dispersion was increased to 125° C., and the contents of the reactor vessel were suspension polymerized at 125° C. for 4 hours. Thereafter, the pH of the content of the reactor vessel was adjusted to be 5.5 or more by adding a sodium hydroxide aqueous solution (in a concentration of 25% by mass) to the reactor vessel, so as to neutralize benzoic acid corresponding to a residue of the polymerization initiator. Then, the content of the reactor vessel was cooled to give the styrene acrylic resin a.
Monomer composition (in molar ratio): styrene/acrylic acid-2-ethylhexyl/1,6-hexanediol diacrylate=82.6/16.9/0.5
A part of the thus obtained styrene acrylic resin a was dissolved in THF (tetrahydrofuran), and the mass average molecular weight of the dissolved styrene acrylic resin a was measured by the GPC. The maximum value of the mass average molecular weight of the styrene acrylic resin a was 1.9×104. Incidentally, the mass average molecular weight was measured by GPC using a detector (“Shodex RI-71” manufactured by Showa Denko K.K.) and a column (“Shodex A-806M” manufactured by Showa Denko K.K.).
(Production of Toner Cores a to D)
Toner cores A to D were produced by using binder resins shown in Table 2 below.
A hundred (100) parts by mass of the corresponding type of binder resin shown in Table 2, 5 parts by mass of a colorant (C.I. Pigment Blue 15:3, copper phthalocyanine), and 5 parts by mass of a release agent (“WEP-3” manufactured by NOF Corporation, ester wax) were mixed by using a mixer (a Henschel mixer) to obtain a mixture. The thus obtained mixture was melt kneaded by using a two screw extruder (“PCM-30” manufactured by Ikegai Corporation) to give a kneaded product. The kneaded product was pulverized by using a mechanical pulverizer (“Turbo Mill” manufactured by Freund Turbo Corporation) to give a pulverized product. The pulverized product was classified by a classifier (“Elbow Jet” manufactured by Nittetsu Mining Co., Ltd.) to obtain a toner core having a volume average particle size (D50) of 6.0 μm and average roundness of 0.93. The volume average particle size of the toner core was measured by using “Coulter Counter Multisizer 3” manufactured by Beckman Coulter. The average roundness of the toner core was measured by using a flow particle image analyzer (“FPIA (registered trademark)-3000” manufactured by Sysmex Corporation).
A part of each of the thus obtained toner cores (the toner cores A to D shown in Table 2) was used for measuring a frictional charge amount attained by using a standard carrier and a zeta potential obtained in a dispersion of pH 4 by methods described below. The frictional charge amounts attained by using the standard carrier and the zeta potentials obtained in a dispersion of pH 4 of the toner cores A to D are shown in Table 2.
<Method for Measuring Frictional Charge Amount Attained by Using Standard Carrier>
A hundred (100) parts by mass of a standard carrier N-01 (a standard carrier for a negatively chargeable toner) available from The Imaging Society of Japan, and 7 parts by mass of the corresponding type of toner core were mixed for 30 minutes by using a Turbula mixer. The thus obtained mixture was used as a measurement sample to measure the frictional charge amount. More specifically, with respect to each measurement sample, the frictional charge amount of the toner core attained through friction with the standard carrier was measured by using a QM meter (“MODEL 210HS-2A” manufactured by TREK Inc.).
<Method for Measuring Zeta Potential Obtained in Dispersion of pH 4>
Zero point two (0.2) g of the corresponding type of toner core, 80 g of ion-exchanged water, and 20 g of 1 mass % nonionic surfactant (polyvinylpyrrolidone, “K-85” manufactured by Nippon Shokubai Co., Ltd.) were mixed by using a magnetic stirrer. Thus, the toner cores were homogeneously dispersed in the liquid to obtain a dispersion. Thereafter, dilute hydrochloric acid was added to the dispersion to adjust the pH of the dispersion to 4. Thus, a toner core dispersion of pH 4 was obtained. By using the toner core dispersion of pH 4 as a measurement sample, a zeta potential was measured. Specifically, the zeta potential of the toner core contained in the measurement sample was measured by using a zeta potential and particle size analyzer (“Delsa Nano HC” manufactured by Beckman Coulter).
(Preparation of Resin Dispersion a)
A polyester resin d having the following monomer composition and having physical properties as shown in Table 1 was used as a binder resin.
Monomer composition (in molar ratio): polyoxypropylene (2,2)-2,2-bis(4-hydroxyphenyl)propane/polyoxyethylene (2,0)-2,2-bis(4-hydroxyphenyl)propane/fumaric acid/trimellitic acid=25/25/46/4
The polyester resin d was primarily pulverized to an average particle size of approximately 10 μm by using “Turbo Mill T250” manufactured by Freund Turbo Corporation. A hundred (100) g of the thus obtained primarily pulverized product of the polyester resin d, 2 g of an anionic surfactant (“Emal E-27C” manufactured by Kao Corporation, sodium polyoxyethylene lauryl ether sulfate), and 50 g of a 0.1 N-sodium hydroxide aqueous solution (a basic substance) were mixed, and ion-exchanged water used as an aqueous medium was further added thereto, thereby preparing a slurry in a total amount of 500 g.
The thus obtained slurry was put in a round-bottom stainless steel pressure vessel. Thereafter, the slurry was subjected to shear dispersion for 30 minutes, by using a high-speed shearing emulsifier, Clearmix (“CLM-2.2S” manufactured by M Technique Co., Ltd.) at a temperature of 145° C., a pressure of 0.5 MPa (G), and a rotor rotational speed of 20,000 rpm. After the shear dispersion, while cooling the slurry at a rate of 5° C./min, the slurry was continuously stirred at a rotor rotational speed of 15,000 rpm until the temperature within the stainless steel vessel reached 50° C. Thereafter, the slurry was cooled to ordinary temperature at a rate of 5° C./min. To the slurry cooled to ordinary temperature, ion-exchanged water was added to attain a solid content concentration, to the mass of the dispersion, of 5% by mass, and thus, a resin dispersion a in which fine particles of the polyester resin were dispersed. The fine particles of the polyester resin contained in the resin dispersion a had an average particle size of approximately 140 nm. The particle size was measured by using a particle size analyzer (“Microtrac UPA 150” manufactured by Nikkiso Co., Ltd.).
(Preparation of Resin Dispersion b)
A resin dispersion b containing fine particles of the styrene acrylic resin b having the physical properties as shown in Table 1 was prepared by suspension polymerization.
A 1000 mL four-necked flask equipped with a stirrer, a cooling tube, a nitrogen introducing tube, and a temperature sensor was charged with 550 mL of distilled water and 0.35 g of an anionic surfactant (“Emal 0” manufactured by Kao Corporation, sodium lauryl sulfate). The contents of the flask were heated to 80° C. under nitrogen stream and stirring, and then, 81 g of a potassium persulfate aqueous solution in a concentration of 2.5% by mass was added to the flask. Furthermore, a monomer mixture containing 89 g of styrene, 58 g of n-butyl acrylate, 14 g of methacrylic acid, and 3.3 g of n-octyl mercaptan was added dropwise by using a dropping funnel to the flask over 1.5 hours. After the dropwise addition, the polymerization reaction was performed at 80° C. for 2 hours while stirring the reaction solution. After completing the polymerization reaction, the content of the flask was cooled to room temperature, and distilled water was added to the flask to attain a solid content concentration of 5% by mass. In this manner, the resin dispersion b in which fine particles of the styrene acrylic resin having an average particle size of approximately 90 nm were dispersed was obtained.
(Preparation of Release Dispersion)
Two hundred (200) g of a release agent having a melting temperature of 84° C. (“WEP-5” manufactured by NOF Corporation, pentaerythritol behenic acid ester wax), 2 g of an anionic surfactant (“Emal E-27C” manufactured by Kao Corporation), and 800 g of ion-exchanged water were mixed. The thus obtained mixture was heated to 100° C. to melt the release agent. The resultant was emulsified for 5 minutes by using a homogenizer (“Ultra-Turrax T50” manufactured by IKA). Subsequently, an emulsification treatment was performed at 100° C. by using Gaulin Homogenizer (manufactured by Manton Gaulin). Thus, a release dispersion having an average particle size of 250 nm, a melting point of 83° C., and a solid content concentration of 20% by mass was obtained.
(Preparation of Coloring Dispersion)
Ninety (90) g of a cyan colorant (C.I. Pigment Blue 15:3, copper phthalocyanine), 10 g of an anionic surfactant (“Emal 0” manufactured by Kao Corporation, sodium lauryl sulfate), and 400 g of ion-exchanged water were mixed. The thus obtained mixture was emulsified and dispersed for 1 hour by using a high-pressure impact disperser, Ultimizer (“HJP30006” manufactured by Sugino Machine Limited). Thus, a coloring dispersion having a solid content concentration of 18% by mass was obtained.
The size distribution of the fine particles of the colorant contained in the thus obtained coloring dispersion was measured by using a particle size analyzer (“Microtrac UPA 150” manufactured by Nikkiso Co., Ltd.). The volume average particle size (MV) of the colorant fine particles contained in the coloring dispersion was 160 nm, and a Cv value of the size distribution was 25%. On the basis of a TEM image of the colorant fine particles, the roundness of the colorant fine particles was confirmed as 0.800.
(Production of Toner Cores E and F)
A dispersion containing a toner core E and a dispersion containing a toner core F were respectively prepared by using the corresponding types of resin dispersions (having a solid content concentration of 5% by mass) shown in Table 3.
A temperature sensor, a cooling tube, and a stirrer were set on a 1 L four-necked flask. Then, 425 g of the corresponding type of resin dispersion (having a solid content concentration of 5% by mass) shown in Table 3, 12.5 g of the release dispersion (having a solid content concentration of 20% by mass), 7 g of the coloring dispersion (having a solid content concentration of 18% by mass), 12 g of an anionic surfactant (“Emal 0” manufactured by Kao Corporation), and 43.5 g of ion-exchanged water were put in the flask, and the contents of the flask were stirred at a stirring rate of 200 rpm. Thereafter, the pH of the content of the flask was adjusted to 9 by using triethanolamine.
Subsequently, an aqueous solution of 10.2 g of magnesium chloride hexahydrate (an aggregating agent) dissolved in 10.2 g of ion-exchanged water was added to the flask. After allowing the dispersion to stand still in the flask for 5 minutes, the temperature within the flask was increased to 50° C. at a rate of 5° C./min Thereafter, the temperature within the flask was further increased to 73° C. at a rate of 0.5° C./min. Subsequently, with the temperature of the dispersion retained at 73° C., aggregation of the fine particles contained in the dispersion was proceeded. When the volume average particle size of aggregated particles contained in the dispersion reached 6.5 μm, 29.3 g of sodium chloride (an aggregation terminator) was added, and the resulting dispersion was stirred at a stirring rate of 350 rpm for 10 minutes. After stirring, the dispersion was cooled to room temperature at a rate of 5° C./min. In this manner, a dispersion containing a toner core having a volume average particle size of 6.6 μm, a number average particle size of 5.7 μm, and average roundness of 0.93 was obtained. Besides, a part of the thus obtained dispersion containing the toner core was used for measuring a zeta potential of the toner core in a dispersion of pH 4 by the aforementioned method.
The toner core was collected from the obtained dispersion of the toner core by a method described below. With respect to the toner core collected from the dispersion, the frictional charge amount of the toner core attained by using the standard carrier was measured by the aforementioned method. The frictional charge amounts attained by using the standard carrier, and the zeta potentials in a dispersion of pH 4 of the toner cores E and F are shown in Table 3.
<Method for Collecting Toner Core>
A wet cake of the toner core was filtered out from the dispersion of the toner core by using a filter cloth having an opening of 1 μm. Thereafter, the wet cake of the toner core was dispersed in ion-exchanged water again to wash the toner core. The toner core was washed by repeating such filtration and dispersion five times. A wet cake of the washed toner core was vacuum dried at 40° C. Thus, a dried toner core was obtained.
For the formation of a shell layer, the following thermoplastic resins a to d were used.
The thermoplastic resin a was a water soluble polyacrylamide (“BECKAMINE A-1” manufactured by DIC Corporation, an aqueous solution having a solid content concentration of 11% by mass).
The thermoplastic resin b was an acrylamide copolymer (having a solid content concentration of 5% by mass) having a monomer composition, a glass transition point (Tg), and a mass average molecular weight as follows:
Monomer composition (in molar ratio): 2-hydroxyethyl methacrylate/acrylamide/methacrylic acid-methoxy polyethylene glycol=30/50/20
Glass transition point (Tg): 110° C.
Mass average molecular weight: 55,000
The thermoplastic resin c was a silicone-acrylic graft copolymer (“Symac US-480” manufactured by Toagosei Co., Ltd., an aqueous solution having a solid content concentration of 25% by mass).
The thermoplastic resin d was a water soluble urethane resin (“Super Flex 170” manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd., an aqueous solution having a solid content concentration of 30% by mass).
(Shell Layer Forming Process)
A 1 L three-necked flask equipped with a thermometer and a stiffing blade was charged with 300 mL of ion-exchanged water. Subsequently, the temperature within the flask was retained at 30° C. by using a water bath. Then, dilute hydrochloric acid was added to the flask to adjust the pH of an aqueous medium contained in the flask to 4. After adjusting the pH, 2 mL of a methylol melamine aqueous solution (“mirben resin SM-607” manufactured by Showa Denko K.K., having a solid content concentration of 80% by mass) and 2 mL of an aqueous solution of the thermoplastic resin a (i.e., an aqueous solution of the water soluble polyacrylamide having a solid content concentration of 11% by mass) were added to the flask as materials of the shell layer (shell materials). Then, the contents of the flask were stirred for dissolving the materials of the shell layer in the aqueous medium. In this manner, a shell layer material aqueous solution (A) was obtained.
To the aqueous solution (A), 300 g of the corresponding type of toner core shown in Table 4 was added, and the contents of the flask were stirred at a stirring rate of 200 rpm for 1 hour. Subsequently, 300 mL of ion-exchanged water was added to the flask. Then, while stirring the contents of the flask at 100 rpm, the temperature within the flask was increased to 70° C. (that is, a shell layer forming temperature) at a rate of 1° C./min. Thereafter, the contents of the flask were continuously stirred at 70° C. and 100 rpm for 2 hours. After stirring, the pH of the content of the flask was adjusted to 7 by adding sodium hydroxide to the flask. Then, the content of the flask was cooled to room temperature. In this manner, a dispersion containing toner mother particles having a zeta potential as shown in Table 4 was obtained.
(Washing Process)
A wet cake of the toner mother particles was filtered out by using a Buchner funnel from the dispersion containing the toner mother particles. The wet cake of the toner mother particles was dispersed again in ion-exchanged water for washing the toner mother particles. Such filtration and dispersion were repeated five times to wash the toner mother particles.
In the washing process performed in the preparation of the toner of Preparation Example 1-1, a filtrate of the dispersion containing the toner mother particles and washing water used in the washing process were collected as drainage. The amount of the collected drainage was 97 parts by mass based on 100 parts by mass of the toner obtained after a drying process described below. The concentration of total organic carbon (TOC) contained in the collected drainage was 8 mg/L. The concentration of the total organic carbon contained in the drainage was measured by using a TOC analyzer (“TOC-4200” manufactured by Shimadzu Corporation).
(Drying Process)
A slurry was prepared by dispersing the wet cake of the toner mother particles in an ethanol aqueous solution in a concentration of 50% by mass. The thus obtained slurry was supplied to a continuous surface modifying apparatus (“Coatmizer” manufactured by Freund Industrial Co., Ltd.) to dry the toner mother particles contained in the slurry. In this manner, dried toner mother particles were obtained. The drying conditions employed in using Coatmizer were a hot air temperature of 45° C. and a blower air flow rate of 2 m3/min
(External Addition Process)
A hundred (100) parts by mass of the toner mother particles resulting from the drying process and 1.0 part by mass of silica (“REA90” manufactured by Nippon Aerosil Co., Ltd.) were mixed for 5 minutes by using a 10 L Henschel mixer for adhering the external additive to the toner mother particles. Thereafter, the resultant toner particles were sifted by a 200 mesh sieve (having an opening of 75 μm).
Toners of Preparation Examples 1-7 to 1-9 were obtained in the same manner as in Preparation Example 1-5 except that the amount of the methylol melamine aqueous solution to be used and the amount of the thermoplastic resin a (the polyacrylamide aqueous solution) to be used were changed to those shown in Table 5.
A toner of Preparation Example 2-1 was obtained in the same manner as in Preparation Example 1-5 except that the amount of the methylol melamine aqueous solution to be used was changed to that shown in Table 5 and that no thermoplastic resin aqueous solution was used.
A toner of Preparation Example 2-2 was obtained in the same manner as in Preparation Example 1-5 except that no methylol melamine aqueous solution was used and that the amount of the aqueous solution of the thermoplastic resin a to be used was changed to that shown in Table 5.
A toner of Preparation Example 1-10 was obtained in the same manner as in Preparation Example 1-5 except that 4 mL of an aqueous solution of a glyoxal monomer (“BECKAMINE NS-11” manufactured by DIC Corporation, having a solid content concentration of 40% by mass) was used instead of the methylol melamine aqueous solution and that 2 mL of a complex metal catalyst aqueous solution (“CATALIST GT-3” manufactured by DIC Corporation) was used together with the glyoxal monomer aqueous solution.
A toner of Preparation Example 1-11 was obtained in the same manner as in Preparation Example 1-5 except that 4 mL of an aqueous solution of a methylolated urea (“BECKAMINE J-300S” manufactured by DIC Corporation, having a solid content concentration of 70% by mass) was used instead of the methylol melamine aqueous solution and that 2 mL of an organic amine catalyst aqueous solution (“CATALIST 376” manufactured by DIC Corporation) was used together with the methylolated urea aqueous solution.
Toners of Preparation Examples 1-12 to 1-14 were obtained in the same manner as in Preparation Example 1-5 except that the types of materials of the shell layer (shell materials) were changed to those shown in Table 6.
Toners of Preparation Examples 1-15 and 1-16 were obtained in the same manner as in Preparation Example 1-5 except that the amount of the methylol melamine aqueous solution to be used and the amount of the thermoplastic resin a (the polyacrylamide aqueous solution) to be used were changed to those shown in Table 7.
<<Thickness of Shell Layer>>
A TEM photograph of a cross-section of a toner particle contained in each of the toners of Preparation Examples 1-1 to 1-16 and Preparation Example 2-1 was taken by a method described below. Incidentally, the toner of Preparation Example 2-2 had no shell in a desired state because the thermoplastic resin alone was used for forming the shell layer. Therefore, the thickness of the shell layer was not measured in the toner of Preparation Example 2-2. On the basis of the TEM photograph of the cross-section of the toner particle, the thickness of the shell layer was measured by a method described below. The thicknesses of the shell layers of the toners of Preparation Examples 1-1 to 1-16 and 2-1 are shown in Tables 4 to 7.
<Method for Taking TEM Photograph of Cross-Section of Toner Particle>
First, each toner was dispersed in a cold-setting epoxy resin, and the resultant was allowed to stand still in an atmosphere of 40° C. for 2 days to give a cured substance. The cured substance was dyed with osmium tetroxide. Thereafter, a thin sample with a thickness of 200 nm for observing the cross-section of a toner particle was cut out from the resulting cured substance by using a microtome (“EM UC6” manufactured by Leica). The thus obtained thin sample was observed with magnifying powers of 3000 and 10000 by using a transmission electron microscope (TEM) (“JSM-6700F” manufactured by JEOL Ltd.) to take a TEM photograph of the cross-section of the toner particle.
<Method for Measuring Thickness of Shell Layer>
The thickness of the shell layer was measured by analyzing the TEM photograph image of the cross-section of the toner particle by using image analysis software (“WinROOF” manufactured by Mitani Corporation). Specifically, two straight lines were drawn to cross at substantially the center of the cross-section of the toner particle, and the lengths of four sections of the two straight lines crossing the shell layer were measured. An average of the thus measured lengths of the four sections was defined as the thickness of the shell layer of one toner particle to be measured. This measurement of the thickness of the shell layer was performed on ten toner particles, so as to obtain an average of the thicknesses of the shell layers of the plural toner particles to be measured. The thus obtained average was determined as the thickness of the shell layer of the toner.
<<Evaluation 1>>
With respect to the toners of Preparation Examples 1-1 to 1-16, 2-1 and 2-2, the high-temperature preservability was evaluated by a method described below. The evaluation results of the high-temperature preservability of the toners of Preparation Examples 1-1 to 1-16, 2-1 and 2-2 are shown in Tables 4 to 7.
<Evaluation of High-Temperature Preservability>
Two (2) g of each toner was weighed in a 20 mL plastic vessel, and the resultant was allowed to stand still for 3 hours in a thermostat heated at 60° C. Thus, a toner for high-temperature preservability evaluation was obtained. Then, the toner for high-temperature preservability evaluation was sifted by using a 100 mesh sieve (having an opening of 150 μm) under conditions of a rheostat scale of 5 and time of 30 seconds in accordance with an instruction manual of a powder tester (manufactured by Hosokawa Micron K.K.). After sifting, the mass of the toner remaining on the sieve was measured. On the basis of the mass of the toner before sifting and the mass of the toner remaining on the sieve after sifting, a degree of aggregation (% by mass) was obtained in accordance with the following formula. On the basis of the calculated degree of aggregation, the high-temperature preservability was evaluated in accordance with the following criteria.
(Calculation Formula for Degree of Aggregation)
Degree of aggregation (% by mass)=100×mass of toner remaining on sieve/mass of toner before sifting
Good (G): The degree of aggregation was 20% by mass or less.
Normal (N): The degree of aggregation was more than 20% by mass, and 50% by mass or less.
Poor (P): The degree of aggregation was more than 50% by mass.
<<Evaluation 2>>
The toners of Preparation Examples 1-1 to 1-16, 2-1 and 2-2 were used for evaluating the low-temperature fixability by a method described below. The low-temperature fixability was evaluated by using a two-component developer prepared as described below. The evaluation results of the low-temperature fixability of the toners of Preparation Examples 1-1 to 1-16, 2-1 and 2-2 are shown in Tables 4 to 7.
A developer carrier (a carrier for TASKalfa 5550) and each of the toners in an amount of 10% by mass based on the mass of the carrier were mixed for 30 minutes by using a ball mill. In this manner, a two-component developer was prepared.
<Evaluation of Low-Temperature Fixability>
As an evaluation apparatus, a printer (“FSC-5250DN” manufactured by Kyocera Document Solutions Inc.) modified so that a fixing temperature could be adjusted was used. The two-component developer prepared in Production Example 8 was supplied to a developing unit of the evaluation apparatus, and the toner was supplied to a toner container of the evaluation apparatus. The linear speed of the evaluation apparatus was set to 200 mm/sec and the toner placement amount of the evaluation apparatus was set to 1.0 mg/cm2, and an unfixed solid image was formed on a recording medium. The unfixed solid image thus formed was fixed with the fixing temperature of a fixing unit of the evaluation apparatus increased from 100° C. in increments of 5° C. in a range of the fixing temperature from 100° C. inclusive to 200° C. inclusive. Thus, a lowest temperature at which the solid image could be fixed on a recording medium without offset was obtained as a lowest fixing temperature. The low-temperature fixability was evaluated in accordance with the following criteria:
Good (G): The lowest fixing temperature was 160° C. or less.
Poor (P): The lowest fixing temperature was more than 160° C.
In each of Preparation Examples 1-1 to 1-16 (Examples 1 to 16), the toner particle contained in the toner includes the toner core containing the binder resin, and the shell layer coating the surface of the toner core. Besides, the shell layer contains a unit derived from the monomer of the thermosetting resin and a unit derived from the thermoplastic resin. Furthermore, the thermosetting resin is one or more resins selected from the group of amino resins consisting of a melamine resin, a urea resin, and a glyoxal resin. These toners of Preparation Examples 1-1 to 1-16 are excellent in the high-temperature preservability and the low-temperature fixability as shown in Tables 4 to 7.
In Preparation Example 2-1 (Comparative Example 1), the toner particle contained in the toner includes the shell layer containing the resin not having a unit derived from a thermoplastic resin. This toner of Preparation Example 2-1 is poor in the low-temperature fixability as shown in Table 5. More specifically, in the toner of Preparation Example 2-1, even if a temperature and a pressure are applied to the toner particle in a fixing operation, the shell layer is not easily broken, and hence the toner cannot be fixed at a low temperature. This is probably because a shell layer containing merely a unit derived from a monomer of a thermosetting resin does not contain a unit derived from a thermoplastic resin, and therefore, the resulting shell layer is highly crosslinked and hence is lowered in the flexibility.
In Preparation Example 2-2 (Comparative Example 2), the toner is produced by using the thermoplastic resin alone in the shell layer forming process. The toner of Preparation Example 2-2 thus obtained is poor in the high-temperature preservability as shown in Table 5. Since a crosslinking reaction between molecules of the thermoplastic resin cannot be caused by using merely the thermoplastic resin, it seems that the toner of Preparation Example 2-2 does not have a shell layer coating the toner core in a desired state. Therefore, in Preparation Example 2-2, a component such as the release agent contained in the toner core easily exude to the surface of the toner particle. This is probably because the high-temperature preservability of the toner of Preparation Example 2-2 is lowered.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2013-134258 | Jun 2013 | JP | national |
| Number | Name | Date | Kind |
|---|---|---|---|
| 4576890 | Hosoi | Mar 1986 | A |
| 4980257 | Anno et al. | Dec 1990 | A |
| 20050271964 | Etou et al. | Dec 2005 | A1 |
| Number | Date | Country |
|---|---|---|
| 559-166966 | Sep 1984 | JP |
| H01-185650 | Jul 1989 | JP |
| 2004-138985 | May 2004 | JP |
| 2004-177660 | Jun 2004 | JP |
| 2010-145555 | Jul 2010 | JP |
| 2013-114228 | Jun 2013 | JP |
| Entry |
|---|
| An Office Action; “Notice of Reasons for Rejection,” issued by the Japanese Patent Office on Jul. 28, 2015, which corresponds to Japanese Patent Application No. 2013-134258 and is related to U.S. Appl. No. 14/316,195. |
| Number | Date | Country | |
|---|---|---|---|
| 20150004540 A1 | Jan 2015 | US |
