Patent Application
20160077455
This patent application is based on and claims priority pursuant to 35 U.S.C. §119(a) to Japanese Patent Application Nos. 2014-186581, filed on Sep. 12, 2014, respectively, in the Japan Patent Office, the entire disclosure of each of which is hereby incorporated by reference herein.
1. Technical Field
The present disclosure relates to a toner for use in electrophotography, electrostatic recording, electrostatic printing, etc. The present disclosure further relates to a method of manufacturing the toner, a developer using the toner.
2. Description of the Related Art
In electrophotography, electrostatic recording, electrostatic printing, etc., a toner is once adhered to a latent image bearer, such as an electrostatic latent image bearer, on which an electrostatic latent image has been formed in a process called developing process. The toner is then transferred from the electrostatic latent image bearer onto a transfer medium such as paper in a process called transfer process. The toner is then fixed on the transfer medium in a process called fixing process. In the fixing process, the toner is generally melted by contact with a heated roller or belt, which is an advantageous method in terms of thermal efficiency. (This method is hereinafter referred to as contact heating fixing method.)
However, the contact heating fixing method is likely to cause an offset phenomenon in which toner is disadvantageously adhered to the heated roller or belt.
In attempting to prevent the occurrence of the offset phenomenon, toners containing a release agent, such as a wax, have been proposed. For example, a toner containing a wax having a predetermined endothermic peak observable by differential scanning calorimetry has been proposed. As another example, a toner containing a candelilla wax, a higher fatty acid wax, a higher alcohol wax, a plant natural wax (e.g., carnauba wax, rice wax), or a montan wax has been proposed.
In the contact heating fixing method, the release agent is melted in a rapid manner when the toner passes through the heated roller or belt. The release agent is thereby exposed at the surface of the toner. The exposed release agent prevents the toner from adhering to the fixing member (i.e., the roller or belt). The release agent exerts influence on the occurrence of both a cold offset phenomenon, which is occurred at low temperatures, and a hot offset phenomenon, which is occurred at high temperatures.
In a case in which the release agent is positioned near the surface of the toner for the purpose of accelerating exposure of the release agent, the occurrence of the offset phenomenon can be prevented, but the release agent will have come to adhere to other members while the toner is being stirred in a developing device. The toner will be pressed against carrier particles or photoconductors and firmly adhere thereto, causing decrease in charge quantity. The release agent should be protected inside the toner when the toner is being stirred or stored. On the other hand, the release agent should be efficiently exposed at the surface of the toner in such a short time during which the toner passes through the fixing member.
Many attempts have been made to determine a proper dispersion particle diameter for the release agent dispersed in the toner for preventing the occurrence of the offset problem while maintaining toner granularity. It is generally very difficult to contain the wax in the form of fine particles inside the toner without exposing them at the surface of the toner because the wax particles are inevitably finer than the toner particles. Furthermore, it affects the environmental charge stability that the wax is positioned near the surface of the toner. For example, increasing of the exposure of the wax deteriorate charge stability at high temperature and high humidity. It causes scattering of toner particles or forms white spots in a image.
From the standpoint of giving resistance to the offset phenomenon to the toner, it is more effective that the release agent exists in the form of a relatively large block rather than in the form of fine particles locally distributed over the toner.
Accordingly, there has been a demand for a toner which achieves a good combination of offset resistance and durability with a small amount of release agent, furthermore stability of an image quality in high temperature high humidity or in low temperature low humidity environment.
In accordance with some embodiments of the present invention, a toner is provided. The toner includes a binder resin and a release agent, wherein the binder resin includes a polyester resin. The toner satisfies the following (1) and (2);
(1) The toner has a single exothermic peak measured by a differential scanning calorimetry (DSC) descending in a temperature range of from 150° C. to 0° C., wherein the exothermic peak is in a temperature range of from 40° C. to 60° C. and has a half bandwidth of at most 10° C.
(2) The release agent disperse to network form in the cross-sectional images of the toner observed with a transmission electron microscope (TEM).
In accordance with some embodiments of the present invention, a developer is provided. The developer includes the above toner and a carrier.
In accordance with some embodiments of the present invention, a method of manufacturing the above toner is provided.
A more complete appreciation of the disclosure and many of the attendant advantages thereof will be readily obtained as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings, wherein:
Embodiments of the present invention are described in detail below with reference to accompanying drawings. In describing embodiments illustrated in the drawings, specific terminology is employed for the sake of clarity. However, the disclosure of this patent specification is not intended to be limited to the specific terminology so selected, and it is to be understood that each specific element includes all technical equivalents that operate in a similar manner and achieve a similar result.
For the sake of simplicity, the same reference number will be given to identical constituent elements such as parts and materials having the same functions and redundant descriptions thereof omitted unless otherwise stated.
One object of the present invention is to provide a toner which has a good combination of offset resistance, environmental charge stability, and image quality stability, and is capable of providing high-definition high-quality image for an extended period of time.
In accordance with some embodiments of the present invention, a toner is provided which has a good combination of offset resistance, environmental charge stability, and image quality stability, and is capable of providing high-definition high-quality image for an extended period of time.
The toner according to an embodiment of the present invention includes a binder resin and a release agent, wherein the binder resin includes a polyester resin. The toner satisfies the following (1) and (2);
(1) The toner has a single exothermic peak measured by a differential scanning calorimetry (DSC) descending in a temperature range of from 150° C. to 0° C., wherein the exothermic peak is in a temperature range of from 40° C. to 60° C. and has a half bandwidth of at most 10° C.
(2) The release agent disperse to network form in the cross-sectional images of the toner observed with a transmission electron microscope (TEM).
When the toner satisfies the above (1) and (2), the toner has good environmental charge stability and has stress resistance as a developer, by dispersing the release agent finely and uniformly in the toner, and by positioning a release agent in the toner in such a way that the toner strength will not be damaged.
Furthermore, the toner has a good offset resistance, by dispersing the release agent to network form in the toner in such a way that the release agent will efficiently exude from the toner in a fixing period.
The toner according to an embodiment of the present invention satisfies the following (1);
(1) The toner has a single exothermic peak measured by a differential scanning calorimetry (DSC) descending in a temperature range of from 150° C. to 0° C., wherein the exothermic peak is in a temperature range of from 40° C. to 60° C. and has a half bandwidth of at most 10° C.
When a half bandwidth is exceeds 10° C., environmental charge stability and image quality stability of the toner may deteriorate, by disturbing uniform crystal growth of the release agent.
The DSC measurement instrument for measuring a exothermic peak is preferably a highly precise inner heat type input compensation differential scanning calorimeter, for example DSC60 from Shimadzu Corporation.
The measurement procedure is based on ASTM D3418-82.
In a nitrogen atmosphere, 5.0 mg of the toner is heated from room temperature to 150° C. at a heating rate of 10° C./min, cooled from 150° C. to 0° C. at a cooling rate of 10° C./min, during which a DSC curve is measured.
From the obtained DSC curve of cooling period, a peak which calorific value is 0.4 J/g or more can be determined as the exothermic peak. The exothermic peak temperature is defined as a vertex temperature of the exothermic peak.
In accordance with some embodiments of the present invention, the exothermic peak is single in a range of from 40° C. to 60° C.
The exothermic peak is a peak of the re-crystallization to come from the crystal materials such as the release agent. Recrystallizing in an approximately same temperature zone shows uniform crystal growth of the crystal materials.
When a plurality of peaks are observed regardless of the kind and the number of contained crystal materials, environmental charge stability of the toner may deteriorate, by disturbing uniform crystal growth of the crystal materials.
The toner according to an embodiment of the present invention satisfies the following (2);
(2) The release agent disperse to network form in the cross-sectional images of the toner observed with a transmission electron microscope (TEM).
In this case, “network form” means that the linear release agent intersects each other and forms two-dimensional network form in a whole cross-sectional image of the toner.
In this case, “forms to two-dimensional network form in a whole cross-sectional image” means that there is little uneven presence state of the release agent in a 2-4 divided regions of an image, when the areas of the divided regions can be made almost equal to each other.
When the release agent is positioned locally, stable fixation property and image quality stability of the toner may deteriorate, because the release agent is not positioned in the toner in such a way that the toner strength will not be damaged and the release agent will not efficiently exude from the toner in a fixing period.
More concretely, for example as shown in
This is not a network form defined in accordance with some embodiments of the present invention.
Furthermore, preferably, the release agent has an average aspect ratio of at least 31 in the toner.
The average aspect ratio is determined from cross-sectional images of the toner observed with a transmission electron microscope (TEM).
As a TEM observation, for example, the toner is embedded in an epoxy resin and cut into ultrathin sections with an ultramicrotome.
The ultrathin sections are observed with a transmission electron microscope at a magnification that the aspect ratio of the release agent is measurable.
Fifty randomly-selected cross-sectional surfaces of the toner are sampled.
The images of the sampled cross-sectional surfaces are analyzed by a software program, for example ImageJ, and subjected to a measurement of the aspect ratio of the release agent in a manner described below.
The aspect ratio of each release agent domain is calculated by dividing its long diameter L1 by its short diameter Ls.
The average aspect ratio is defined as the average among the aspect ratios of the release agent domains having the maximum long diameter in each of the fifty randomly-selected cross-sectional surfaces of the toner.
Prior to the TEM observation, the ultrathin sections are dyed with ruthenium and/or osmium so as to enhance contrast of the release agent domains.
How to measure the aspect ratio of the release agent in the toner is explained with reference to
The short diameter Ls is defined as the average length of four lines (Ls1 to Ls4) drawn from the points equally dividing the long diameter L1 into five sections in a direction perpendicular to the long diameter L1.
In a case in which multiple release agent domains are overlapped with each other in each cross-sectional surface, the multiple release agent domains overlapped with each other is regarded as a single release agent domain.
In a case in which any of the lines Ls1 to Ls4 is overlapped with a branched part of a release agent domain, as shown in a dotted circle in
In accordance with some embodiments of the present invention, preferably, the average aspect ratio of the release agent is at least 31.
When the average aspect ratio falls below 31, it is likely that the release agent is exposed at the surface of the toner, and toner charge deterioration and background fouling may occur upon bleeding of the release agent.
Additionally, the particle strength of the toner may deteriorate.
Preferably, the average aspect ratio is from 31 to 50.
The toner according to an embodiment of the present invention, the average aspect ratio of the release agent can be at least 31, for example, by comprising a vinyl graft polymer which becomes compatible with the release agent. The vinyl graft polymer is described later.
In accordance with some embodiments of the present invention, preferably, the release agent is a wax, and the content of the wax in the toner is from 1% to 20% by mass, when the content is converted from an endothermic quantity of the toner determined by a differential scanning calorimetry (DSC).
Additionally, preferably, the amount of the wax existing in a region ranging from the surface to 0.3 μm in depth of the toner is less than 0.5% by mass, when the amount is determined by an attenuated total reflection infrared spectroscopy (FTIR-ATR).
How to measure the amount of the wax is described in detail below.
The total amount of the wax in the toner is measured by a differential scanning calorimetry (DSC).
The toner and the wax alone are each subjected to a measurement of endothermic quantity under the following conditions.
Measuring Device:
Differential scanning calorimeter (DSC60 from Shimadzu Corporation)
Amount of sample: About 5 mg
Heating rate: 10° C./min
Measuring range: From room temperature to 150° C.
Measuring environment: In nitrogen gas atmosphere
The total amount of the wax is calculated from the following formula (6).
Total Amount of Wax (% by mass)=(Endothermic Quantity of Wax in Toner (J/g)×100)/(Endothermic Quantity of Wax Alone (J/g))
Even if the outflow of the wax has occurred in the toner production process and not all the raw-material wax is incorporated in the resulting toner, the total amount of the wax contained in the resulting toner can be effectively determined by the above procedure.
The amount of the wax existing at the surface of the toner is measured by an attenuated total reflection Fourier transform infrared spectroscopy (FTIR-ATR).
According to the measurement principle of FTIR-ATR, the measuring depth is about 0.3 μm.
Thus, the amount of the wax existing in a region ranging from the surface to 0.3 μm in depth of the toner can be measured.
The measuring procedure is as follows.
First, 3 g of the toner is pelletized for 1 minute at a load of 6 t using an automatic pelletizer (Type M No. 50 BRP-E from Maekawa Testing Machine Mfg. Co., LTD.) and formed into a pellet having a diameter of 40 mm and a thickness of about 2 mm.
The surface of the pellet is subject to a measurement with FTIR-ATR.
As the measuring device, a microscopic FTIR device SPECTRUM ONE (from PerkinElmer Inc.) equipped with an ATR unit is used. The measurement is performed in micro ATR mode using a germanium (Ge) crystal having a diameter of 100 μm.
The incidence angle of infrared ray is set to 41.5°, the resolution is set to 4 cm-1, and the cumulated number is set to 20.
The intensity ratio of the peak arising from the wax to that arising from the binder resin is defined as the relative amount of the wax existing at the surface of the toner.
The measurement is repeated four times changing the measuring position.
The measured values are averaged.
The absolute amount of the wax existing at the surface of the toner is determined from the relative amount thereof with reference to a calibration curve compiled from several samples in which a known amount of the wax is uniformly dispersed in the binder resin.
The wax existing in the region ranging from the surface to 0.3 μm in depth of the toner can smoothly exude from the toner and effectively exert toner releasability.
Preferably, the amount of the wax existing at the surface of the toner measured by the FTIR-ATR is less than 0.5% by mass, more preferably from 0.1% to less than 0.5% by mass.
When the amount of the wax existing at the surface of the toner is at least 0.1% by mass, it means that the wax existing near the surface of the toner is not insufficient.
Thus, the toner can exert sufficient releasability when being fixed.
When the amount of the wax existing at the surface of the toner is less than 0.5% by mass, it means that the wax existing near the surface of the toner is not excessive.
Thus, the wax is not exposed at the outermost surface of the toner.
The wax will not accelerate adhesion of the toner to carrier particles and will not deteriorate filming resistance of the developer.
Additionally, since the wax is not exposed at the outermost surface of the toner, the wax will not deteriorate charge stability of the toner.
To achieve a good combination of offset resistance, chargeability, developability, and filming resistance, the amount of the wax existing at the surface of the toner is preferably less than 0.5% by mass.
Preferably, the total amount of the wax measured by the DSC is from 1% to 20% by mass.
When the total amount of the wax in the toner is at least 1% by mass, it means that the wax contained in the toner is not insufficient.
Thus, the toner can exert sufficient releasability when being fixed without degrading offset resistance.
When the total amount of the wax in the toner is at most 20% by mass, filming resistance and color image gloss will not deteriorate, which is preferable.
More preferably, the total amount of the wax measured by the DSC is from 3% to 10% by mass.
More further preferably, the total amount of the wax measured by the DSC is from 5% to 8% by mass.
In accordance with some embodiments of the present invention, preferably, the wax contains a C30-C50 monoalkyl ester compound.
More preferably, the wax contains a C34-C42 monoalkyl ester compound.
The monoalkyl ester compound is produced through, for example, esterification reaction between a long-chain aliphatic carboxylic acid component and a long-chain aliphatic alcohol component.
For example, the esterification between a rather-high-purity long-chain aliphatic carboxylic acid (whose alkyl group has about 15 to about 30 carbon atoms, for example) and a high-purity long-chain aliphatic alcohol (whose alkyl group has about 14 to about 34 carbon atoms, for example) gives a mixture of monoalkyl ester compounds having a narrow distribution of the number of carbon atoms.
The mixture of the monoalkyl ester compounds having a narrow distribution of the number of carbon atoms has a narrow range of melting point and also a low viscosity.
This mixture contains a small amount of components evaporated at low temperatures and is easily separated from toner particles when heated, and thus is excellent in releaseability.
The C30-C50 monoalkyl ester compound are not particularly limited and may be appropriately selected depending on the intended purpose.
Examples thereof include compounds represented by the following General Formula (I):
Ra-COO—Rb (I)
where Ra represents a C15-C30 alkyl group and Rb represents a C14-C34 alkyl group.
Further examples of the monoalkyl ester compounds contained in the release agent include ester compounds synthesized through esterification reaction between a monofunctional long-chain aliphatic carboxylic acid and a monofunctional long-chain aliphatic alcohol.
Examples of the monofunctional long-chain aliphatic carboxylic acid include nonadecanoic acid, eicosanoic acid, heneicosanoic acid, docosanoic acid, tetracosanoic acid, pentacosanoic acid, hexacosanoic acid, heptacosanoic acid, octacosanoic acid, nonacosanoic acid, triacontanoic acid, myristic acid, palmitic acid, stearic acid, arachidenic acid and behenic acid, with stearic acid, behenic acid and myristic acid being preferred.
Examples of the monofunctional long-chain aliphatic alcohol include eicosane-1-ol (eicosanol), myristyl alcohol, cetyl alcohol, palmityl alcohol, stearyl alcohol, arachidel alcohol and behenyl alcohol, with steary alcohol, eicosanol and cetyl alcohol being preferred.
In the monoalkyl ester compounds, for example, Ra is preferably a C15-C30 linear alkyl group (a long-chain aliphatic group), more preferably a C17-C21 linear alkyl group (a long-chain aliphatic group).
Also, Rb is preferably a C14-C34 linear alkyl group (a long-chain aliphatic group), more preferably a C14-C20 linear alkyl group (a long-chain aliphatic group).
The release agent contains, as main components, the C30-C50 monoalkyl ester compound.
Other types of the release agent (e.g., paraffins) may be contained therein, so long as fixability/releaseability, less contamination against a charging member and durability of the formed toner are maintained to satisfactory levels.
The release agent preferably has a melting point of at least 65° C., more preferably from 69° C. to 120° C., to balance fixability and offset resistance.
When the melting point is at least 65° C., the blocking resistance may not deteriorate.
The melting point of the release agent is defined as a temperature at which the maximum endothermic peak is observed in an endothermic curve of the release agent measured by differential scanning calorimetry (DSC).
Preferably, the melting point of the release agent or toner is measured with a high-precision inner-heat power-compensation differential scanning calorimeter based on a method according to ASTM D3418-82.
The endothermic curve is obtained by preliminarily heating and cooling a sample and then heating the sample at a heating rate of 10° C./min.
The toner preferably has a volume average particle diameter of from 1 μm to 8 μm so as to form high-resolution high-definition high-quality image.
The particle size distribution (i.e., the ratio of the volume average particle diameter to the number average particle diameter) of the toner is preferably from 1.00 to 1.15 so as to produce reliable image for an extended period of time.
In particular, the toner has a volume-based particle size distribution in which a second peak is observed at a particle diameter 1.21 to 1.31 times the model diameter.
When the second peak does not exist, and especially when the ratio of the volume average particle diameter to the number average particle diameter is near 1.00 (i.e., monodisperse), it means that the toner is very likely to take a close-packing structure, which causes degradation in initial flowability and cleanability.
Toner Composition
The toner according to an embodiment of the present invention includes at least a binder resin and a release agent, wherein the binder resin includes a polyester resin, and optionally other components such as a colorant, a colorant dispersant, and a charge controlling agent.
The toner may further include a flowability improver and/or a cleanability improver on its surface, if needed.
Binder Resin
The binder resin other than a polyester resin is not limited to any particular resin so long it is soluble in an organic solvent.
Specific examples of the binder resin include, but are not limited to, a vinyl polymer or copolymer obtainable from a styrene monomer, an acrylic monomer, and/or a methacrylic monomer, polyol resin, phenol resin, silicone resin, polyurethane resin, polyamide resin, furan resin, epoxy resin, xylene resin, terpene resin, coumarone indene resin, polycarbonate resin, and petroleum resin.
Specific examples of a constituent monomer of the polyester resin include, but are not limited to, a divalent alcohol such as ethylene glycol, propylene glycol, 1,3-butanediol, 1,4-butanediol, 2,3-butanediol, diethylene glycol, triethylene glycol, 1,5-pentanediol, 1,6-hexanediol, neopentyl glycol, 2-ethyl-1,3-hexanediol, hydrogenated bisphenol A, and a diol obtained from a polymerization between bisphenol A and a cyclic ether (e.g., ethylene oxide, propylene oxide).
By using a polyol having 3 or more valences or an acid having 3 or more valences in combination, the resulting polyester resin can have a cross-linked structure.
The used amount of such a polyol or an acid should be controlled such that the resulting resin is not prevented from being dissolved in an organic solvent.
Specific examples of the polyol having 3 or more valences include, but are not limited to, sorbitol, 1,2,3,6-hexanetetrol, 1,4-sorbitan, pentaerythritol, dipentaerythritol, tripentaerythritol, 1,2,4-butanetriol, 1,2,5-pentanetriol, glycerol, 2-methylpropanetriol, 2-methyl-1,2,4-butanetriol, trimethylolethane, trimethylolpropane, and 1,3,5-trihydroxybenzene.
Specific examples of acid for producing the polyester resin include, but are not limited to, a benzene dicarboxylic acid (e.g., phthalic acid, isophthalic acid, terephthalic acid) and an anhydride thereof, an alkyl dicarboxylic acid (e.g., succinic acid, adipic acid, sebacic acid, azelaic acid) and an anhydride thereof, an unsaturated dibasic acid (e.g., maleic acid, citraconic acid, itaconic acid, alkenyl succinic acid, fumaric acid, mesaconic acid), and an unsaturated dibasic acid anhydride (e.g., maleic acid anhydride, citraconic acid anhydride, itaconic acid anhydride, alkenyl succinic acid anhydride).
Specific examples of the polycarboxylic acid having 3 or more valences include, but are not limited to, trimellitic acid, pyromellitic acid, 1,2,4-benzenetricarboxylic acid, 1,2,5-benzenetricarboxylic acid, 2,5,7-naphthalenetricarboxylic acid, 1,2,4-naphthalenetricarboxylic acid, 1,2,4-butanetricarboxylic acid, 1,2,5-hexanetricarboxylic acid, 1,3-dicarboxyl-2-methyl-2-methylenecarboxypropane, tetra(methylenecarboxy)methane, 1,2,7,8-octanetetracarboxylic acid, enpol trimmer acid, and anhydrides and partial lower alkyl esters of these compounds.
When the binder resin is a polyester resin, a molecular weight distribution of THF solubles in the resin which is measured by gel permeation chromatography (GPC) has at least one peak at a number average molecular weight of from 3,000 to 50,000 from the viewpoint of fixability and offset resistance of the toner.
Preferably, the content ratio of THF solubles having a molecular weight of 100,000 or less in the binder resin is from 70% to 100% from the viewpoint of discharge performance.
More preferably, the molecular weight distribution of the binder resin has at least one peak at a molecular weight of from 5,000 to 20,000.
In the present disclosure, the molecular weight distribution of the binder resin is measured by gel permeation chromatography (GPC) using THF as a solvent.
When the binder resin is a polyester resin, the polyester resin preferably has an acid value of from 0.1 mgKOH/g to 100 mgKOH/g, more preferably from 0.1 mgKOH/g to 70 mgKOH/g, and most preferably from 0.1 mgKOH/g to 50 mgKOH/g.
In the present disclosure, the acid value of the binder resin component in the toner composition is measured based on the following method according to JIS K-0070.
(1) A measurement sample is prepared by previously removing components other than the binder resin (polymer) component from the toner composition, or previously measuring the acid values and contents of the components other than the binder resin (polymer) content in the toner composition.
The measurement sample, having been pulverized, in an amount of from 0.5 g to 2.0 g is precisely weighed.
This weight is identified as the polymer component weight W (g).
For example, to measure the acid value of the binder resin in the toner, the acid values and contents of a colorant, a magnetic material, etc., should be previously measured so that the acid value of the binder resin can be calculated.
(2) The measurement sample is dissolved in 150 ml of a mixed liquid of toluene/ethanol (volume ratio: 4/1) in a 300-ml beaker.
(3) The resulting solution is subjected to a titration with a 0.1 mol/l ethanol solution of KOH using a potentiometric titrator.
(4) The consumed amount of the KOH solution in the titration is identified as S (ml).
The consumed amount of the KOH solution in a blank titration is identified as B (ml).
The acid value can be calculated from the following formula (C).
In the formula (C), f represents the factor of KOH.
Acid Value(mgKOH/g)=[(S−B)×f×5.61]/W (C)
Specific examples of the styrene monomer include, but are not limited to, styrene, o-methylstyrene, m-methylstyrene, p-methylstyrene, p-phenylstyrene, p-ethylstyrene, 2,4-dimethylstyrene, p-n-amylstyrene, p-tert-butylstyrene, p-n-hexylstyrene, p-n-octylstyrene, p-n-nonylstyrene, p-n-decylstyrene, p-n-dodecylstyrene, p-methoxystyrene, p-chlorostyrene, 3,4-dichlorostyrene, m-nitrostyrene, o-nitrostyrene, p-nitrostyrene, and derivatives thereof.
Specific examples of the ester of acrylic acid include, but are not limited to, methyl acrylate, ethyl acrylate, propyl acrylate, n-butyl acrylate, isobutyl acrylate, n-octyl acrylate, n-dodecyl acrylate, 2-ethylhexyl acrylate, stearyl acrylate, 2-chloroethyl acrylate, and phenyl acrylate.
Specific examples of the ester of methacrylic acid include, but are not limited to, methyl methacrylate, ethyl methacrylate, propyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, n-octyl methacrylate, n-dodecyl methacrylate, 2-ethylhexyl methacrylate, stearyl methacrylate, phenyl methacrylate, dimethyl aminoethyl methacrylate, and diethyl aminoethyl methacrylate.
The following monomers can also be used for preparing the vinyl polymer or copolymer.
(1) Monoolefins such as ethylene, propylene, butylene, and isobutylene.
(2) Polyenes such as butadiene and isoprene.
(3) Vinyl halides such as vinyl chloride, vinylidene chloride, vinyl bromide, and vinyl fluoride.
(4) Vinyl esters such as vinyl acetate, vinyl propionate, and vinyl benzoate.
(5) Vinyl ethers such as vinyl methyl ether, vinyl ethyl ether, and vinyl isobutyl ether.
(6) Vinyl ketones such as vinyl methyl ketone, vinyl hexyl ketone, and methyl isopropenyl ketone.
(7) N-Vinyl compounds such as N-vinyl pyrrole, N-vinyl carbazole, N-vinyl indole, and N-vinyl pyrrolidone.
(8) Vinyl naphthalenes.
(9) Acrylic or methacrylic acid derivatives such as acrylonitrile, methacrylonitrile, and acrylamide.
(10) Unsaturated dibasic acids such as maleic acid, citraconic acid, itaconic acid, an alkenyl succinic acid, fumaric acid, and mesaconic acid.
(11) Unsaturated dibasic anhydrides such as maleic anhydride, citraconic anhydride, itaconic anhydride, an alkenyl succinic anhydride.
(12) Unsaturated dibasic acid monoesters such as maleic acid monomethyl ester, maleic acid monoethyl ester, maleic acid monobutyl ester, citraconic acid monomethyl ester, citraconic acid monoethyl ester, citraconic acid monobutyl ester, itaconic acid monomethyl ester, alkenyl succinic acid monomethyl ester, fumaric acid monomethyl ester, and mesaconic acid monomethyl ester.
(13) Unsaturated dibasic acid esters such as dimethyl maleate and dimethyl fumarate.
(14) α,β-Unsaturated acids such as crotonic acid and cinnamic acid.
(15) α,β-Unsaturated anhydrides such as crotonic anhydride and cinnamic anhydride.
(16) Monomers having carboxyl group such as anhydrides of α,β-unsaturated acids with lower fatty acids, anhydrides and monoesters of alkenyl malonic acid, alkenyl glutaric acid, and alkenyl adipic acid.
(17) Hydroxyalkyl esters of acrylic or methacrylic acids such as 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, and 2-hydroxypropyl methacrylate.
(18) Monomers having hydroxyl group such as 4-(1-hydroxy-1-methylbutyl)styrene, 4-(1-hydroxy-1-methylhexyl)styrene.
The vinyl polymer or copolymer may have a cross-linked structure formed by a cross-linker having two or more vinyl groups.
Specific examples of the cross-linker include, but are not limited to:
aromatic divinyl compounds such as divinylbenzene and divinylnaphthalene;
diacrylate and dimethacrylate compounds bonded with an alkyl chain, such as ethylene glycol diacrylate, 1,3-butylene glycol diacrylate, 1,4-butanediol diacrylate, 1,5-pentanediol diacrylate, 1,6-hexanediol diacrylate, neopentyl glycol diacrylate, ethylene glycol dimethacrylate, 1,3-butylene glycol dimethacrylate, 1,4-butanediol dimethacrylate, 1,5-pentanediol dimethacrylate, 1,6-hexanediol dimethacrylate, and neopentyl glycol dimethacrylate;
and diacrylate and dimethacrylate compounds bonded with an alkyl chain having ether bond, such as diethylene glycol diacrylate, triethylene glycol diacrylate, tetraethylene glycol diacrylate, polyethylene glycol #400 diacrylate, polyethylene glycol #600 diacrylate, dipropylene glycol diacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacrylate, tetraethylene glycol dimethacrylate, polyethylene glycol #400 dimethacrylate, polyethylene glycol #600 dimethacrylate, and dipropylene glycol dimethacrylate.
Specific examples of the cross-linker further include diacrylate and dimethacrylate compounds bonded with a chain having an aromatic group and ether bond.
Specific examples of the cross-linker further include polyester-type diacrylate compounds such as MANDA (available from Nippon Kayaku Co., Ltd.).
Specific examples of the cross-linker further include polyfunctional cross-linkers such as pentaerythritol triacrylate, trimethylolethane triacrylate, trimethylolpropane triacrylate, tetramethylolmethane tetraacrylate, oligoester acrylate, pentaerythritol trimethacrylate, trimethylolethane trimethacrylate, trimethylolpropane trimethacrylate, tetramethylolmethane tetramethacrylate, oligoester methacrylate, triallyl cyanurate, and triallyl trimellitate.
Among these cross-linkers, aromatic divinyl compounds (especially divinylbenzene) and diacrylate compounds bonded with a chain having an aromatic group are preferable from the viewpoint of fixability and offset resistance of the binder resin.
In particular, combinations of monomers which produce a styrene copolymer or styrene-acrylic copolymer are preferable.
Specific examples of a polymerization initiator for use in preparation of the vinyl polymer or copolymer include, but are not limited to, 2,2′-azobisisobutyronitrile, 2,2′-azobis(4-methoxy-2,4-dimethylvaleronitrile), 2,2′-azobis(2,4-dimethylvaleronitrile), 2,2′-azobis(2-methylbutyronitrile), dimethyl-2,2′-azobisisobutyrate, 1,1′-azobis(1-cyclohexanecarbonitrile), 2-(carbamoylazo)-isobutyronitrile, 2,2′-azobis(2,4,4-trimethylpentane), 2-phenylazo-2′,4′-dimethyl-4′-methoxyvaleronitrile, 2,2′-azobis(2-methylpropane), methyl ethyl ketone peroxide, acetylacetone peroxide, cyclohexanone peroxide, 2,2-bis(tert-butylperoxy)butane, tert-butyl hydroperoxide, cumene hydroperoxide, 1,1,3,3-tetramethylbutyl hydroperoxide, di-tert-butyl peroxide, tert-butylcumyl peroxide, dicumyl peroxide, α-(tert-butylperoxy)isopropyl benzene, isobutyl peroxide, octanoyl peroxide, decanoyl peroxide, lauroyl peroxide, 3,5,5-trimethylhexanoyl peroxide, benzoyl peroxide, m-tolyl peroxide, di-isopropyl peroxydicarbonate, di-2-ethylhexyl
peroxydicarbonate, di-n-propyl peroxydicarbonate, di-2-ethoxyethyl peroxycarbonate, di-ethoxyisopropyl peroxydicarbonate, di(3-methyl-3-methoxubutyl) peroxycarbonate, acetylcyclohexylsulfonyl peroxide, tert-butyl peroxyacetate, tert-butyl peroxyisobutyrate, tert-butyl peroxy-2-ethyl hexanoate, tert-butyl peroxylaurate, tert-butyl oxybenzoate, tert-butyl peroxyisopropyl carbonate, di-tert-butyl peroxyisophthalate, tert-butyl peroxyallyl carbonate, isoamyl peroxy-2-ethyl hexanoate, di-tert-butyl peroxyhexahydroterephthalate, and tert-butyl peroxyazelate.
When the binder resin is a styrene-acrylic resin, a molecular weight distribution of tetrahydrofuran (THF) solubles in the resin which is measured by gel permeation chromatography (GPC) has at least one peak at a number average molecular weight of from 3,000 to 50,000.
Preferably, the vinyl polymer includes a vinyl graft polymer having a main chain consisting of a resin (A) and a graft chain consisting of a resin (B).
The resin (A) is not limited to any particular resin so long as the resin (B) can be grafted.
Specific examples of the resin (A) include, but are not limited to, a polyolefin resin and a thermal degradation polyolefin resin.
Specific examples of the olefin composing the polyolefin resin include, but are not limited to, ethylene, propylene, 1-butene, 1-isobutylene, 1-hexene, 1-dodecene, and 1-octadecene.
Specific examples of the polyolefin resin include, but are not limited to, an olefin polymer, an olefin polymer oxide, a modified olefin polymer, and a copolymer of the olefin with another monomer polymerizable with the olefin.
Specific examples of the olefin polymer include, but are not limited to, polyethylene, polypropylene, ethylene/propylene copolymer, ethylene/1-butene copolymer, and propylene/1-hexene copolymer.
Specific examples of the olefin polymer oxide include, but are not limited to, an oxide of the olefin polymer.
Specific examples of the modified olefin polymer include, but are not limited to, a maleic acid derivative (e.g., maleic anhydride, monomethyl maleate, monobutyl maleate, dimethyl maleate) adduct of the olefin polymer.
Specific examples of the copolymer of the olefin with another monomer include, but are not limited to, a copolymer of the olefin with an unsaturated carboxylic acid (e.g., acrylic acid, methacrylic acid, itaconic acid, maleic anhydride) or an unsaturated carboxylic acid alkyl ester (e.g., an acrylic acid alkyl (C1-C18) ester, a methacrylic acid alkyl (C1-C18) ester, a maleic acid alkyl (C1-C18) ester).
The monomers do not necessarily have an olefin structure so long as the polymer has an olefin structure.
For example, a polymethylene (e.g., SASOL wax) can be used.
Among the above polyolefin resins, olefin polymers, olefin polymer oxides, and modified olefin polymers are preferable;
polyethylene, polymethylene, polypropylene, ethylene/propylene copolymer, oxidized polyethylene, oxidized polypropylene, and maleated polypropylene are more preferable;
and polyethylene and polypropylene are most preferable.
Specific examples of monomers for producing the resin (B) include, but are not limited to, an unsaturated carboxylic acid alkyl (C1-C5) ester (e.g., methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, butyl acrylate, butyl methacrylate, 2-ethylhexyl acrylate, 2-ethylhexyl methacrylate) and a vinyl ester monomer (e.g., vinyl acetate).
Among these monomers, an alkyl acrylate or methacrylate is preferable, and an alkyl acrylate or methacrylate (B 1) in which the alkyl chain has 1 to 5 carbon atoms is preferable.
An aromatic vinyl monomer (B2) is used in combination with the alkyl acrylate or methacrylate (B1) to produce the resin (B).
Specific examples of the aromatic vinyl monomer (B2) include, but are not limited to, a styrene monomer (e.g., styrene, α-methylstyrene, p-methylstyrene, m-methylstyrene, p-methoxystyrene, p-hydroxystyrene, p-acetoxystyrene, vinyl toluene, ethylstyrene, phenylstyrene, benzylstyrene).
Among these monomers, styrene is preferable.
In the present disclosure, it is preferable to contain the vinyl graft polymer in addition to the polyester resin.
The release agent can disperse uniformly and finely in the toner, because the vinyl graft polymer has higher affinity with the release agent comprising the monoalkyl ester than the polyester resin.
The vinyl graft polymer interact with the release agent in a process granulating a toner and can make uniform crystal growth of the release agent by delaying crystallization.
As a result, the toner has a single exothermic peak by growing uniform crystal of the release agent. The release agent disperse to network form in the cross-sectional images of the toner because the vinyl graft polymer restrains the crystal growth of the release agent.
The weight ratio of the vinyl graft polymer to the polyester resin is preferably from 40:60 to 5:95, and more preferably from 20:80 to 5:95.
When the toner comprises more vinyl graft polymer than the weight ratio mentioned above, the toner dose not always exert sufficient releasability when being fixed.
Both the binder resin and the toner composition containing the binder resin preferably have a glass transition temperature (Tg) of from 35° C. to 80° C., more preferably from 40° C. to 70° C. When Tg is less than 35° C., the toner may deteriorate in a high-temperature atmosphere.
When Tg exceeds 80° C., the fixability of the toner may deteriorate.
Colorant
Specific examples of usable colorants include, but are not limited to, carbon black, Nigrosine dyes, black iron oxide, NAPHTHOL YELLOW S, HANSA YELLOW (10G, 5G and G), Cadmium Yellow, yellow iron oxide, loess, chrome yellow, Titan Yellow, polyazo yellow, Oil Yellow, HANSA YELLOW (GR, A, RN and R), Pigment Yellow L, BENZIDINE YELLOW (G and GR), PERMANENT YELLOW (NCG), VULCAN FAST YELLOW (5G and R), Tartrazine Lake, Quinoline Yellow Lake, ANTHRAZANE YELLOW BGL, isoindolinone yellow, red iron oxide, red lead, orange lead, cadmium red, cadmium mercury red, antimony orange, Permanent Red 4R, Para Red, Fire Red, p-chloro-o-nitroaniline red, Lithol Fast Scarlet G, Brilliant Fast Scarlet, Brilliant Carmine BS, PERMANENT RED (F2R, F4R, FRL, FRLL and F4RH), Fast Scarlet VD, VULCAN FAST RUBINE B, Brilliant Scarlet G, LITHOL RUBINE GX, Permanent Red F5R, Brilliant Carmine 6B, Pigment Scarlet 3B, Bordeaux 5B, Toluidine Maroon, PERMANENT BORDEAUX F2K, HELIO BORDEAUX BL, Bordeaux 10B, BON MAROON LIGHT, BON MAROON MEDIUM, Eosin Lake, Rhodamine Lake B, Rhodamine Lake Y, Alizarine Lake, Thioindigo Red B, Thioindigo Maroon, Oil Red, Quinacridone Red, Pyrazolone Red, polyazo red, Chrome Vermilion, Benzidine Orange, perynone orange, Oil Orange, cobalt blue, cerulean blue, Alkali Blue Lake, Peacock Blue Lake, Victoria Blue Lake, metal-free Phthalocyanine Blue, Phthalocyanine Blue, Fast Sky Blue, INDANTHRENE BLUE (RS and BC), Indigo, ultramarine, Prussian blue, Anthraquinone Blue, Fast Violet B, Methyl Violet Lake, cobalt violet, manganese violet, dioxane violet, Anthraquinone Violet, Chrome Green, zinc green, chromium oxide, viridian, emerald green, Pigment Green B, Naphthol Green B, Green Gold, Acid Green Lake, Malachite Green Lake, Phthalocyanine Green, Anthraquinone Green, titanium oxide, zinc oxide, and lithopone. Two or more of these colorants can be used in combination.
The content of the colorant in the toner is preferably from 1% to 15% by mass and more preferably from 3% to 10% by mass.
The colorant can be combined with a resin to be used as a master batch. Specific examples of the resin for use in the master batch include, but are not limited to, polyester resin mentioned above, polymers of styrene and derivatives thereof (e.g., polystyrene, poly-p-chlorostyrene, polyvinyl toluene), styrene copolymers (e.g., styrene-p-chlorostyrene copolymer, styrene-propylene copolymer, styrene-vinyl toluene copolymer, styrene-vinylnaphthalene copolymer, styrene-methyl acrylate copolymer, styrene-ethyl acrylate copolymer, styrene-butyl acrylate copolymer, styrene-octyl acrylate copolymer, styrene-methyl methacrylate copolymer, styrene-ethyl methacrylate copolymer, styrene-butyl methacrylate copolymer, styrene-methyl α-chloromethacrylate copolymer, styrene-acrylonitrile copolymer, styrene-vinyl methyl ketone copolymer, styrene-butadiene copolymer, styrene-isoprene copolymer, styrene-acrylonitrile-indene copolymer, styrene-maleic acid copolymer, styrene-maleate copolymer), polymethyl methacrylate, polybutyl methacrylate, polyvinyl chloride, polyvinyl acetate, polyethylene, polypropylene, polyester, epoxy resin, epoxy polyol resin, polyurethane, polyamide, polyvinyl butyral, polyacrylic acid resin, rosin, modified rosin, terpene resin, aliphatic or alicyclic hydrocarbon resin, aromatic petroleum resin, chlorinated paraffin, and paraffin wax.
Two or more of these resins can be used in combination.
The master batch can be obtained by mixing and kneading a resin and a colorant while applying a high shearing force.
To increase the interaction between the colorant and the resin, an organic solvent can be used.
More specifically, the master batch can be obtained by a method called flushing in which an aqueous paste of the colorant is mixed and kneaded with the resin and the organic solvent so that the colorant is transferred to the resin side, followed by removal of the organic solvent and moisture.
This method is advantageous in that the resulting wet cake of the colorant can be used as it is without being dried.
When performing the mixing or kneading, a high shearing force dispersing device such as a three roll mill can be preferably used.
The content of the master batch is preferably from 0.1 parts to 20 parts by mass based on 100 parts by mass of the binder resin.
The resin for the master batch preferably has an acid value of at most 30 mgKOH/g and an amine value of from 1 to 100.
More preferably, the acid value is at most 20 mgKOH/g and the amine value is from 10 to 50.
When the acid value is at most 30 mgKOH/g, the chargeability may not deteriorate even under high-humidity conditions and sufficient colorant dispersibility is provided.
When the amine value is from 1 to 100, sufficient colorant dispersibility is provided.
The acid value can be measured based on a method according to JIS K-0070.
The amine value can be measured based on a method according to JIS K-7237.
Colorant Dispersion Liquid
The colorant can be used as a colorant dispersion liquid.
Any colorant dispersant can be used.
Dispersants having high affinity for the binder resin are preferable from the viewpoint of colorant dispersibility.
Specific examples of such dispersants include, but are not limited to, commercially available dispersants such as AJISPER PB821 and PB822 (from Ajinomoto Fine-Techno Co., Inc.), DISPERBYK-2001 (from BYK-Chemie GmbH), and EFKA-4010 (from EFKA).
The colorant dispersant preferably has a weight average molecular weight of from 500 to 100,000, which is a styrene-converted local maximum molecular weight at which the main peak is observed in a molecular weight distribution chart obtained by gel permeation chromatography.
From the viewpoint of colorant dispersibility, the molecular weight is more preferably from 3,000 to 100,000, much more preferably from 5,000 to 50,000, and most preferably from 5,000 to 30,000.
When the molecular weight is less than 500, the polarity is so high that the colorant dispersibility may deteriorate.
When the molecular weight exceeds 100,000, the affinity for the solvent is so high that the colorant dispersibility may deteriorate.
The addition amount of the colorant dispersant is preferably from 1 part to 200 parts by mass, more preferably from 5 parts to 80 parts by mass, based on 100 parts by mass of the colorant.
When the addition amount is at least 1 part by mass, the colorant dispersibility may not deteriorate.
When the addition amount is at most 200 parts by mass, chargeability may not deteriorate.
Charge Controlling Agent
Specific examples of the charge controlling agent include, but are not limited to, nigrosine dyes, triphenylmethane dyes, chromium-containing metal complex dyes, chelate pigments of molybdic acid, Rhodamine dyes, alkoxyamines, quaternary ammonium salts (including fluorine-modified quaternary ammonium salts), alkylamides, phosphor and phosphor-containing compounds, tungsten and tungsten-containing compounds, fluorine activators, metal salts of salicylic acid, and metal salts of salicylic acid derivatives. Usable commercially available charge controlling agents include, but are not limited to, BONTRON® 03 (nigrosine dye), BONTRON® P-51 (quaternary ammonium salt), BONTRON® S-34 (metal-containing azo dye), BONTRON® E-82 (metal complex of oxynaphthoic acid), BONTRON® E-84 (metal complex of salicylic acid), and BONTRON® E-89 (phenolic condensation product), which are manufactured by Orient Chemical Industries Co., Ltd.; TP-302 and TP-415 (molybdenum complexes of quaternary ammonium salts), which are manufactured by Hodogaya Chemical Co., Ltd.; COPY CHARGE® PSY VP2038 (quaternary ammonium salt), COPY BLUE® PR (triphenyl methane derivative), COPY CHARGE® NEG VP2036 and COPY CHARGE® NX VP434 (quaternary ammonium salts), which are manufactured by Hoechst AG; LRA-901, and LR-147 (boron complex), which are manufactured by Japan Carlit Co., Ltd.; and copper phthalocyanine, perylene, quinacridone, azo pigments, and polymers having a functional group such as a sulfonate group, a carboxyl group, and a quaternary ammonium group, phenol resins, and fluorine-based compounds.
The used amount of the charge controlling agent is determined depending on the kind of the binder resin, existence or non-existence of an additive, the toner production method including its dispersion method, etc., and is not limited to a particular value.
The used amount of the charge controlling agent is preferably from 0.1 parts to 10 parts by mass, more preferably from 0.2 parts to 5 parts by mass, based on 100 parts by mass of the binder resin.
When the used amount of the charge controlling agent is at most 10 parts by mass, the toner fixability is not inhibited.
From the viewpoint of production stability, the charge controlling agent is preferably used in a state being dissolved in an organic solvent.
Alternatively, the charge controlling agent can be used in a state being finely dispersed in an organic solvent by a bead mill.
The Toner
The toner may further include a flowability improver and/or a cleanability improver on its surface, if needed.
Flowability Improver
The toner may include a flowability improver.
The flowability improver improves flowability of the toner by existing at the surface of the toner.
Specific examples of the fluidity improver include, but are not limited to, a fine powder of silica prepared by a wet process or a dry process;
fine powders metal oxides such as titanium oxide and alumina;
and fine powders of silica, titanium oxide, and alumina which are surface-treated with a silane-coupling agent, a titanium-coupling agent, or a silicone oil;
and fine powders of fluorocarbon resins such as vinylidene fluoride and polytetrafluoroethylene.
Among these materials, fine powders of silica, titanium oxide, and alumina are preferable.
In addition, a fine powder of silica which is surface-treated with a silane-coupling agent or a silicone oil is preferable.
The fluidity improver preferably has an average primary particle diameter of from 0.001 μm to 100 nm and more preferably from 0.002 μm to 50 nm.
The fine powder of silica can be obtained by gas phase oxidation of a silicon halide, and is generally called as dry-method silica or fumed silica.
Specific examples of commercially available fine powder of silica obtained by gas phase oxidation of a silicon halide include, but are not limited to, AEROSIL-130, -300, -380, -TT600, -MOX170, -MOX80, and -COK84 (from Nippon Aerosil Co., Ltd.); CAB-O-SIL-M-5, -MS-7, -MS-75, -HS-5, and -EH-5 (from Cabot Corporation); WACKER HDK-N20V15, -N20E, -T30, and -T40 (from Wacker Chemie AG); D-C Fine Silica (from Dow Corning Corporation); and Fransol (from Fransil).
In addition, a fine powder of hydrophobized silica, obtained by hydrophobizing the fine powder of silica obtained by gas phase oxidation of a silicon halide, is also preferable.
The hydrophobized silica preferably has a hydrophobicity degree of from 30% to 80% measured by a methanol titration test.
Hydrophobicity is given by chemically or physically treating a fine powder of silica with a material which is reactive with or adsorptive to the silica, such as an organic silicon compound.
Treating the fine powder of silica obtained by gas phase oxidation of a silicon halide with an organic silicon compound is preferable.
Specific examples of the organic silicon compound include, but are not limited to, hydroxypropyltrimethoxysilane, phenyltrimethoxysilane, n-hexadecyltrimethoxysilane, n-octadecyltrimethoxysilane, vinylmethoxysilane, vinyltriethoxysilane, vinyltriacetoxysilane, dimethylvinylchlorosilane, divinylchlorosilane, γ-methacryloxypropyltrimethoxysilane, hexamethyldisilane, trimethylsilane, trimethylchlorosilane, dimethyldichlorosilane, methyltrichlorosilane, allyldimethylchlorosilane, allylphenyldichlorosilane, benzyldimethylchlorosilane, bromomethyldimethylchlorosilane, α-chloroethyltrichlorosilane, β-chloroethyltrichlorosilane, chloromethyldimethylchlorosilane, triorganosilylmercaptan, trimethylsilylmercaptan, triorganosilyl acrylate, vinylmethylacetoxysilane, dimethylethoxysilane, trimethylethoxysilane, trimethylmethoxysilane, methyltriethoxysilane, isobutyltrimethoxysilane, dimethyldimethoxysilane, diphenyldiethoxysilane, hexamethyldisiloxane, 1,3-divinyltetramethyldisiloxane, 1,3-diphenyltetramethyldisiloxane, and dimethylpolysiloxane having 2 to 12 siloxane units per molecule and 0 or 1 hydroxyl group bonded to Si in each terminal unit. Other than the above compounds, silicone oils such as dimethyl silicone oil are also usable. Two or more of these compounds can be used in combination.
The fluidity improver preferably has a number average particle diameter of from 5 nm to 100 nm and more preferably from 5 nm to 50 nm.
The fluidity improver preferably has a specific surface area of at least 30 m2/g, more preferably from 60 m2/g to 400 m2/g, measured by the BET method employing nitrogen adsorption.
When the fluidity improver is a surface-treated powder, the fluidity improver preferably has a specific surface area of at least 20 m2/g, more preferably from 40 m2/g to 300 m2/g, measured by the BET method employing nitrogen adsorption.
The used amount of the fluidity improver is preferably from 0.03 parts to 8 parts by mass based on 100 parts by mass of the toner.
Cleanability Improver
The cleanability improver improves removability of residual toner particles remaining on an electrostatic latent image bearer or primary transfer medium after a toner image has been transferred therefrom onto a recording medium.
Specific examples of the cleanability improver include, but are not limited to, metal salts of fatty acids (e.g., zinc stearate, calcium stearate) and fine particles of polymers prepared by soap-free emulsion polymerization (e.g., polymethyl methacrylate, polystyrene).
Preferably, the fine particles of polymers have a relatively narrow size distribution and a volume average particle diameter of from 0.01 μm to 1 μm.
The fluidity improver and cleanability improver are adhered to or fixed on the surface of the toner.
Therefore, they are collectively called as external additives.
The external additives can be added to the toner by, for example, a powder mixer.
Specific examples of the powder mixer include, but are not limited to, a V-type mixer, a Rocking mixer, a Loedige mixer, a Nauta mixer, and a Henschel mixer.
Additionally, HYBRIDIZER, MECHANOFUSION, and Q-MIXER are also usable when the external additive is to be fixed on the surface of the toner.
Developer
In accordance with some embodiments of the present invention, the toner can be used for either one-component developer or two-component developer. The toner can be mixed with a carrier to be used as the two-component developer.
Carrier
Specific examples of the carrier include, but are not limited to, a ferrite carrier, a magnetite carrier, and a resin-coated carrier. The resin-coated carrier is composed of a core particle and a covering material that is a resin covering the core particle. Specific examples of the covering material include, but are not limited to, a styrene-acrylic resin (e.g., styrene-acrylate copolymer, styrene-methacrylate copolymer), an acrylic resin (e.g., acrylate copolymer, methacrylate copolymer), a fluorine-containing resin (e.g., polytetrafluoroethylene, monochlorotrifluoroethylene polymer, polyvinylidene fluoride), a silicone resin, a polyester resin, a polyamide resin, a polyvinyl butyral resin, and an aminoacrylate resin. In addition, an ionomer resin and a polyphenylene sulfide resin are also usable. Two or more of these resins can be used in combination.
Specific examples of the carrier further include a binder-type carrier in which a magnetic powder is dispersed in a resin. With respect to the resin-coated carrier, the surface of the core particle is covered with the resin (covering material) by a method such that the resin is dissolved or suspended in a solvent and then the solution or suspension is applied to the core particle, or the resin and the core particle are merely mixed in a powder state. The content ratio of the covering material is preferably from 0.01% to 5% by mass, more preferably from 0.1% to 1% by mass, based on 100 parts by mass of the resin-coated carrier.
Specific examples the carrier in which a magnetic material is covered with a mixture of two or more kinds of covering materials include, but are not limited to, the following.
(1) A titanium oxide powder in an amount of 100 parts by mass treated with a mixture of methyldichlorosilane and dimethyl silicone oil (at a weight ratio of 1:5) in an amount of 12 parts by mass.
(2) A silica powder in an amount of 100 parts by mass treated with a mixture of dimethyldichlorosilane and dimethyl silicone oil (at a weight ratio of 1:5) in an amount of 20 parts by mass.
Specific examples of the covering material further include, but are not limited to, a styrene-methyl methacrylate copolymer, a mixture of a fluorine-containing resin and a styrene copolymer, and a silicone resin. Among these resins, the silicone resin is preferable.
Specific examples of the mixture of a fluorine-containing resin and a styrene copolymer include, but are not limited to, a mixture of a polyvinylidene fluoride and a styrene-methyl methacrylate copolymer; a mixture of polytetrafluoroethylene and a styrene-methyl methacrylate copolymer; and a mixture of a vinylidene fluoride-tetrafluoroethylene copolymer (at a copolymerization mass ratio of from 10:90 to 90:10), a styrene-2-ethylhexyl acrylate copolymer (at a copolymerization mass ratio of from 10:90 to 90:10), and a styrene-2-ethylhexyl acrylate-methyl methacrylate copolymer (at a copolymerization mass ratio of from 20:60:5 to 30:10:50). Specific examples of the silicone resin include, but are not limited to, a nitrogen-containing silicon resin and a modified silicone resin obtained by reacting a nitrogen-containing silane-coupling agent with a silicone resin.
Specific magnetic materials usable as the core particle include, but are not limited to, an oxide (e.g., ferrite, iron-excess ferrite, magnetite, γ-iron oxide), a metal (e.g., iron, cobalt, nickel), and an alloy thereof. These magnetic materials may include an element such as iron, cobalt, nickel, aluminum, copper, lead, magnesium, tin, zinc, antimony, beryllium, bismuth, calcium, manganese, selenium, titanium, tungsten, and vanadium. Among these magnetic materials, a copper-zinc-iron ferrite composed primarily of copper, zinc, and iron, and a manganese-magnesium-iron ferrite composed primarily of manganese, magnesium, and iron are preferable.
Depending on the surface roughness of the carrier and the content of the covering material, the carrier preferably has a volume resistivity of from 106 Ω·cm to 1010 Ω·cm. The carrier preferably has a particle diameter of from 4 μm to 200 μm, more preferably from 10 μm to 150 μm, and most preferably from 20 μm to 100 μm. In particular, the resin-coated carrier preferably has a 50% particle diameter of from 20 μm to 70 μm. The two-component developer preferably contains the toner in an amount of from 1 part to 200 parts by mass, more preferably from 2 parts to 50 parts by mass, per 100 parts by mass of the carrier.
In a developing method using the toner according to an embodiment of the present invention, any electrophotographic electrostatic latent image bearer can be used. For example, an organic electrostatic latent image bearer, an amorphous silica electrostatic latent image bearer, a selenium electrostatic latent image bearer, and a zinc oxide electrostatic latent image bearer are preferable.
Method of Manufacturing Toner
One example of the method of manufacturing the toner is described below.
The toner according to an embodiment of the present invention can be obtained through the processes of: forming liquid droplets by discharging a toner composition liquid in which the binder resin and the release agent are dissolved or dispersed in a solvent; and solidifying the liquid droplets into fine particles.
Specific examples of the release agent include, but are not limited to, a wax.
Here, the wax is required to be soluble in the toner composition liquid.
Hence, a wax which is soluble in the solvent of the toner composition should be used.
It is possible that the release agent is dissolved in the solvent or the toner composition liquid by application of heat.
To achieve stable continuous discharge, the temperature of the toner composition liquid is less than [Tb-20]° C., where Tb represents the boiling point of the solvent, during the process of solidifying the liquid droplets.
When the temperature of the solvent is less than [Tb-20]° C., generation of bubbles due to vaporization of the solvent in a toner composition liquid chamber or narrowing of discharge holes due to drying up of the toner composition liquid near the discharge holes are prevented and stable discharge can be achieved.
To prevent the release agent from clogging the discharge holes, the release agent needs to be dissolved in the toner composition liquid. At the same time, the release agent also needs to be dissolved in the binder resin being dissolved in the toner composition liquid without causing phase separation, to obtain uniform toner particles. It is also required that the binder resin and the release agent are phase-separated in the resultant toner particles from which the solvent has been removed, so that the toner can exert releasability when being fixed to prevent the occurrence of the offset phenomenon. In case that the release agent and the binder resin are not phase-separated in the toner particles, the toner cannot exert releasability. Moreover, the melt viscosity and elasticity of the binder resin are so decreased that the hot offset phenomenon is likely to occur.
Accordingly, the release agent should be selected depending on the kind of the solvent and binder resin in use.
Solvent
The solvent is not limited to any particular material so long as it is volatile and is capable of dissolving or dispersing the toner composition. Specific preferred examples of the solvent include, but are not limited to, an ether, a ketone, a hydrocarbon, and an alcohol. In particular, tetrahydrofuran (THF), acetone, methyl ethyl ketone (MEK), ethyl acetate, toluene, and water are more preferable. Two or more of these solvents can be used in combination.
Method of Preparing Toner Composition Liquid
The toner composition liquid can be prepared by dissolving or dispersing the toner composition in the solvent. The toner composition is dissolved or dispersed in the solvent by means of a homomixer or a bead mill so that the dispersoids (e.g., a colorant) become finer than the opening diameter of the discharge holes and discharge hole clogging is prevented.
Preferably, the toner composition liquid has a solid content of from 3% to 40% by mass. When the solid content is at least 3% by mass, the productivity does not decrease and the dispersoids (i.e., a colorant) do not settle out or aggregate. As a result, toner particles having a uniform composition can be obtained without degrading the toner quality. When the solid content is at most 40% by mass, toner particles having a small particle diameter are obtainable.
One example of an apparatus for manufacturing the toner according to an embodiment of the present invention is described in detail below with reference to
Liquid Droplet Discharge Device
The liquid droplet discharge device is not limited to any particular device so long as the particle diameter distribution of the discharged liquid droplets is narrow. The liquid droplet discharge device is of several types: a single-fluid nozzle, a two-fluid nozzle, a film-vibration-type discharge device, a Rayleigh-fission-type discharge device, a liquid-vibration-type discharge device, and a liquid-column-resonance-type discharge device. The film-vibration-type liquid droplet discharge device is described in, for example, JP-2008-292976-A, the disclosure of which is incorporated herein by reference. The Rayleigh-fission-type liquid droplet discharge device is described in, for example, JP-4647506-B, the disclosure of which is incorporated herein by reference. The liquid-vibration-type liquid droplet discharge device is described in, for example, JP-2010-102195-A, the disclosure of which is incorporated herein by reference.
To narrow the particle diameter of liquid droplets and secure the productivity of the toner, the liquid-column-resonance-type discharge device is preferably used. In the liquid-column-resonance-type discharge device, a vibration is applied to a liquid contained in a liquid column resonance liquid chamber to form a liquid column resonant standing wave therein, and the liquid is discharged from multiple discharge holes formed within an area corresponding to antinodes of the liquid column resonant standing wave.
Liquid Column Resonance Liquid Droplet Discharge Device
One example of the liquid-column-resonance-type liquid droplet discharge device is described in detail below.
The liquid to be discharged from the liquid droplet discharge device may be, for example, a toner-constituents-containing liquid in which toner constituents are dissolved or dispersed. Since the liquid just has to be in a liquid state and does not necessarily include any solvent, the liquid may take a form of a toner-constituents-melting liquid comprised of the toner constituents in a melted state. Hereinafter both the toner-constituents-containing liquid and the toner-constituents-melting liquid are collectively referred to as the toner composition liquid.
A toner composition liquid 14 is flowed into the liquid common supply path 17 disposed within a liquid droplet formation unit 10, as illustrated in
Within the liquid column resonance liquid chamber 18 filled with the toner composition liquid 14, the vibration generator 20 causes liquid column resonance and generates a pressure standing wave.
Thus, a pressure distribution is formed therein.
The liquid droplets 21 are discharged from the discharge holes 19 provided within an area corresponding to an antinode of the pressure standing wave, where the amplitude in pressure variation is large.
The area corresponding to an antinode is defined as an area not corresponding to a node of the pressure standing wave.
Preferably, the area corresponding to an antinode is an area where the amplitude in pressure variation of the standing wave is large enough to discharge liquid droplets.
More preferably, the area corresponding to an antinode is an area extending from a position at a local maximum amplitude (i.e., a node of the velocity standing wave) toward a position at a local minimum amplitude for a distance ±¼ of the wavelength of the pressure standing wave.
Within the area corresponding to an antinode of the pressure standing wave, even in a case in which multiple discharge holes are provided, each of the multiple discharge holes discharges uniform liquid droplets at a high degree of efficiency without causing clogging. After passing the liquid common supply path 17, the toner composition liquid 14 flows into a liquid return pipe and returns to a raw material container. As the liquid droplets 21 are discharged, the amount of the toner composition liquid 14 in the liquid column resonance liquid chamber 18 is reduced and a suction force generated by the action of the liquid column resonance standing wave is also reduced within the liquid column resonance liquid chamber 18. Thus, the liquid common supply path 17 temporarily increases the flow rate of the toner composition liquid 14 to fill the liquid column resonance liquid chamber 18 with the toner composition liquid 14. After the liquid column resonance liquid chamber 18 is refilled with the toner composition liquid 14, the flow rate of the toner composition liquid 14 in the liquid common supply path 17 is returned.
The liquid column resonance liquid chamber 18 may be formed of joined frames formed of a material having a high stiffness which does not adversely affect liquid resonant frequency of the liquid at drive frequency, such as metals, ceramics, and silicone. A length L between both longitudinal ends of the liquid column resonance liquid chamber 18 illustrated in
The vibration generator 20 is not limited to any particular device so long as it can be driven at a predetermined frequency. For example, the vibration generator 20 may be formed from a piezoelectric body and an elastic plate 9 attached to each other. The elastic plate 9 constitutes a part of the wall of the liquid column resonance liquid chamber 18 so that the piezoelectric body does not contact the liquid. The piezoelectric body may be, for example, a piezoelectric ceramic such as lead zirconate titanate (PZT), which is generally laminated because of having a small displacement. Additionally, piezoelectric polymers such as polyvinylidene fluoride (PVDF), crystals, and single crystals of LiNbO3, LiTaO3, and KNbO3 are also usable. Preferably, the vibration generator 20 in each liquid column resonance liquid chamber 18 is independently controllable. Alternatively, a single blockish vibrating material may be partially cut to fit the arrangement of the liquid column resonance liquid chambers 18 so that each liquid column resonance liquid chamber 18 is independently controllable through the elastic plate.
Each of the discharge holes 19 preferably has an outlet diameter (Dp) of from 1 μm to 40 μm. When Dp is less than 1 μm, the resulting liquid droplets may be too small to be used as a toner. In a case in which the liquid includes solid fine particles of toner constituents, such as pigments, the discharge holes 19 will be clogged frequently and the productivity will decrease. When Dp exceeds 40 μm, the diameter of each liquid droplets may be too large. In case such large liquid droplets are dried and solidified into toner particles having a desired particle diameter of from 1 μm to 8 μm, the toner composition needs to be diluted with an organic solvent. Moreover, a large amount of drying energy is needed to obtain a certain amount of toner, which is not preferable. Arranging the discharge holes 19 in the width direction of the liquid column resonance liquid chamber 18, as illustrated in
The cross-sectional shape of each of the discharge holes 19 has a tapered shape such that the outlet diameter gets smaller, as illustrated in
A mechanism of liquid droplet formation in the liquid droplet formation unit 10 is described in detail below.
First, a mechanism of liquid column resonance generated in the liquid column resonance liquid chamber 18 in the liquid column resonance liquid droplet discharge device 11 is described.
The resonant wavelength λ is represented by the following formula (1):
λ=c/f (1)
wherein c represents a sonic speed in the toner composition liquid in the liquid column resonance liquid chamber 18 and f represents a drive frequency given to the toner composition liquid from the vibration generator 20.
Referring to
L=(N/4)λ (2)
wherein N represents an even number.
The formula (2) is also satisfied when both ends of the liquid column resonance liquid chamber 18 are completely open or free.
Similarly, when one end is open or free so that pressure can be released and the other end is closed or fixed, resonance most effectively occurs when the length L is an odd multiple of λ/4. In this case, the length L is represented by the formula (2) as well, wherein N represents an odd number.
Thus, the most effective drive frequency f is derived from the formulae (1) and (2) and represented by the following formula (3):
f=N×c/(4L) (3)
Actually, vibration is not infinitely amplified because the liquid attenuates resonance due to its viscosity. Therefore, resonance can occur even at a frequency around the most effective drive frequency f represented by the formula (3), as shown in the later-described formula (4) or (5).
In
In acoustics, an open end is defined as a point at which longitudinal velocity of a medium (e.g., a liquid) is maximum and pressure thereof is zero. A closed end is defined as a point at which longitudinal velocity of the medium is zero. The closed end is acoustically considered as a hard wall that reflects waves. When each end is ideally completely closed or open, resonant standing waves as illustrated in
In the liquid column resonance liquid chamber 18 of the liquid column resonance liquid droplet discharge device 11 illustrated in
In particular, the drive frequency depends on the number, arrangement, and/or cross-sectional shape of the discharge holes 19. For example, as the number of the discharge holes 19 increases, closed ends of the liquid column resonance liquid chamber 18 are gradually released from restriction. As a result, a resonant standing wave is generated as if both ends are substantially open and the drive frequency is increased. The restriction releases from the position of one of the discharge holes 19 disposed closest to a liquid supply path 17. As another example, when each of the discharge holes 19 has a round cross-sectional shape or the volume of each discharge hole 19 is varied by varying the frame thickness, the actual standing wave has a short wavelength which has a higher frequency than the drive frequency. Upon application of voltage to the vibration generator 20 with the drive frequency thus determined, the vibration generator 20 deforms so as to generate a resonant standing wave most effectively. A liquid column resonance standing wave can generate even at a frequency around the most effective drive frequency for generating a resonant standing wave. When the vibration generator 20 vibrates at a drive frequency f satisfying the following formulae (4) and (5), a liquid column resonance is generated and liquid droplets are discharged from the discharge holes 19: wherein L represents a length between both longitudinal ends of the liquid column resonance liquid chamber 18 and Le represents a distance between a longitudinal end of the liquid column resonance liquid chamber 18 closer to the liquid common supply path 17 and the discharge hole 19 closest to the longitudinal end.
N×c/(4L)≦f≦N×c/(4Le) (4)
N×c/(4L)≦f≦(N+1)×c/(4Le) (5)
It is preferable that an inequation Le/L>0.6 is satisfied.
Based on the above-described mechanism of liquid column resonance, a liquid column resonant pressure standing wave is formed in the liquid column resonance liquid chamber 18 illustrated in
The liquid column resonance liquid chamber 18 has at least one discharge hole 19, but preferably multiple discharge holes 19 to improve productivity. Preferably, the number of the discharge holes 19 per liquid column resonance liquid chamber 18 is from 2 to 100. When the number of the discharge holes 19 per liquid column resonance liquid chamber 18 is at most 100, a voltage to be applied to the vibration generator 20 in forming liquid droplets from the discharge holes 19 can be reduced and therefore the behavior of the piezoelectric body serving as the vibration generator 20 can be stabilized. Preferably, the interval between adjacent discharge holes 19 is at least 20 μm, and is equal to or less than the length of the liquid column resonance liquid chamber 18. When the interval is at least 20 μm, probability that liquid droplets discharged from adjacent discharge holes collide with each other and form a large liquid droplet can be reduced, resulting in production of toner particles having a proper particle size distribution.
Details of a liquid column resonance phenomenon occurring in the liquid column resonance liquid chamber 18 are described with reference to
In
In
In
Thereafter, as illustrated in
In summary, a liquid column resonant standing wave is generated in the liquid around the discharge holes 19 of the liquid column resonance liquid chamber 18 by a high-frequency driving of the generation vibrator 20. Since the discharge holes 19 are disposed to the position corresponding to antinodes of the standing wave at which the pressure amplitude becomes maximum, the toner liquid droplets 21 are continuously discharged from the discharge holes 19 in accordance with the period of the standing wave.
Solidification of Liquid Droplets
After the liquid droplet discharge device discharges liquid droplets of the toner composition liquid into a gas phase, the liquid droplets are solidified and collected.
Liquid Droplet Solidification Device
The method for solidifying the liquid droplets is selected depending on the nature of the toner composition liquid, and is not limited to a specific method so long as the toner composition liquid can be solidified.
For example, when the toner composition liquid is comprised of a volatile solvent in which solid raw materials are dissolved or dispersed, the discharged liquid droplets can be solidified by drying the liquid droplets, in other words, evaporating the solvent, in a carrier gas flow. The drying condition is controllable by controlling the temperature of the injection gas, vapor pressure, and kind of the gas. The liquid droplets need not necessarily be completely dried so long as the collected particles are kept in a solid state. In this case, the collected particles may be subject to an additional drying process. Alternatively, the drying can be achieved by means of temperature change, chemical reaction, etc.
Toner Collector
The solidified particles can be collected by any powder collector, such as a cyclone collector or a back filter.
Conveyance Airflow
If the injected liquid droplets are brought into contact with each other before being dried, the liquid droplets coalesce with each other to form a single particle. (This phenomenon is hereinafter referred to as “coalescence”.) To obtain toner particles having a uniform particle diameter distribution, it is preferable that the distance between the injected liquid droplets is kept constant. Although the initial velocity is constant, the injected liquid droplet is gradually stalled due to air resistance. As a result, a posterior liquid droplet may catch up on and coalesce with the stalled particle. Because this phenomenon occurs constantly, the particle diameter distribution of the resulting collected particles may become undesirably wide. To prevent coalescence of liquid droplets, liquid droplets should be conveyed to the toner collector 62 by the conveyance airflow 101 while being solidified without being stalled or brought into contact with each other.
Referring back to
It is also possible that coalescence of the liquid droplets is prevented by the first airflow and the solidified particles are conveyed to the toner collector 62 by the second airflow.
It is preferable that the speed of the first airflow be equal to or more than the liquid droplet injection speed. If the speed of the first airflow is smaller than the liquid droplet injection speed, it is difficult for the first airflow (coalescence preventing airflow) to achieve its purpose, i.e., to prevent coalescence of the liquid droplets.
The first airflow can have any additional property for preventing coalescence of the liquid droplets and does not necessarily have the same property as the second airflow. In the first airflow (coalescence preventing airflow), a chemical substance which accelerates solidification of the liquid droplets can be mixed. Additionally, the first airflow (coalescence preventing airflow) can be physically treated to have a function of accelerating solidification of the liquid droplets.
The conveyance airflow 101 is not limited in condition, and may be, for example, a laminar flow, a swirl flow, or a turbulent flow. The conveyance airflow 101 is not limited in substance, and may be formed of, for example, the air or a noncombustible gas such as nitrogen. The temperature of the conveyance airflow 101 is variable but is preferably constant during the manufacturing operation. The chamber 61 may further include a unit for changing the condition of the conveyance airflow 101. The conveyance airflow 101 may prevent not only the coalescence of the liquid droplets 21 but also the adhesion of the liquid droplets 21 to the chamber 61.
Secondary Drying
When toner particles collected in the drying collecting unit 60 illustrated in
Having generally described this invention, further understanding can be obtained by reference to certain specific examples which are provided herein for the purpose of illustration only and are not intended to be limiting. In the descriptions in the following examples, “part(s)” described in Examples means “part(s) by mass.”, unless otherwise specified.
Stearic acid (special grade reagent, product of Kishida Chemical Co., Ltd.) (284 g, 1 mol), stearyl alcohol (special grade reagent, product of Kishida Chemical Co., Ltd.) (256 g, 1 mol) and sulfuric acid (20 mL) are placed in a round-bottom flask equipped with a stirrer and a condenser, followed by refluxing at 130 C for 4 hours while the formed water is being removed.
The resultant product is purified with dimethyl ether to thereby obtain WAX 1.
Behenic acid (EP grade, product of Tokyo Chemical Industry Co., Ltd.) (340 g, 1 mol), cetyl alcohol (special grade reagent, product of Kishida Chemical Co., Ltd.) (242 g, 1 mol) and sulfuric acid (20 mL) are placed in a round-bottom flask equipped with a stirrer and a condenser, followed by refluxing at 130 C for 4 hours while the formed water is being removed.
The resultant product is purified with diisopropyl ether to thereby obtain WAX 2.
Behenic acid (EP grade, product of Tokyo Chemical Industry Co., Ltd.) (340 g, 1 mol), stearyl alcohol (special grade reagent, product of Kishida Chemical Co., Ltd.) (256 g, 1 mol) and sulfuric acid (20 mL) are placed in a round-bottom flask equipped with a stirrer and a condenser, followed by refluxing at 150 C for 5 hours while the formed water is being removed.
The resultant product is purified with diisopropyl ether to thereby obtain WAX 3.
Behenic acid (EP grade, product of Tokyo Chemical Industry Co., Ltd.) (340 g, 1 mol), eicosanol (EP grade, product of Tokyo Chemical Industry Co., Ltd.) (284 g, 1 mol) and sulfuric acid (20 mL) are placed in a round-bottom flask equipped with a stirrer and a condenser, followed by refluxing at 200 C for 5 hours while the formed water is being removed.
The resultant product is purified with diisopropyl ether to thereby obtain WAX 4.
Stearic acid (special grade reagent, product of Kishida Chemical Co., Ltd.) (284 g, 1 mol), cetyl alcohol (special grade reagent, product of Kishida Chemical Co., Ltd.) (242 g, 1 mol) and sulfuric acid (20 mL) are placed in a round-bottom flask equipped with a stirrer and a condenser, followed by refluxing at 200 C for 5 hours while the formed water is being removed.
The resultant product is purified with diisopropyl ether to thereby obtain WAX 5.
The following Table 1 shows the carbon number distribution of each of the above-produced synthetic ester waxes WAX 1 to WAX 5 (i.e., the amounts (% by mass) of monoalkyl ester compounds having carbon atoms whose numbers are shown in Table 1).
The following Table 1 shows the melting point of each of the above-produced synthetic ester waxes WAX 1 to WAX 5 measured by differential scanning calorimetry (DSC).
The carbon number distribution of each synthetic ester wax is measured through 13C-NMR using a nuclear magnetic resonance spectrometer (product of JEOL Ltd.).
The number of carbon of monoalkyl ester compound is defined as the number of carbon having the highest component ratio among the carbon number distribution.
Preparation of Colorant Dispersion Liquid
A carbon black dispersion liquid is prepared as follows.
First, 20 parts of a carbon black (REGAL 400 from Cabot Corporation) and 2 parts of a colorant dispersant (AJISPER PB821 from Ajinomoto Fine-Techno Co., Inc.) are primarily dispersed in 78 parts of ethyl acetate using a mixer having stirrer blades. The resulting primary dispersion liquid is subjected to a dispersion treatment using a DYNOMILL to more finely disperse the carbon black and completely remove aggregations by application of a strong shearing force. The resulting secondary dispersion liquid is filtered with a polytetrafluoroethylene (PTFE) filter (Fluoropore™ Membrane Filter FHLP09050 available from Nihon Millipore K.K.) having a pore size of 0.45 μm to further disperse the carbon black to submicron range. Thus, a carbon black dispersion liquid is prepared.
Preparation of Toner Composition Liquid
First, 20 parts of a WAX 1, 243.3 parts of a polyester resin A, and 20 parts of a vinyl graft polymer 1 are mixed and dissolved in 676.7 parts of ethyl acetate using a mixer having stirrer blades.
All of the WAX 1, the polyester resin A and the vinyl graft polymer 1 are dissolved in the ethyl acetate without causing phase separation and a transparent liquid is obtained.
After adjusting the temperature of the liquid to 55° C., 100 parts of the carbon black dispersion liquid are mixed therein and stirred for 10 minutes.
Thus, a toner composition liquid is prepared.
The polyester resin A is a binder resin synthesized from terephthalic acid, succinic acid, and propylene glycol, having a weight average molecular weight (Mw) of 24,000 and a glass transition temperature (Tg) of 65° C.
The vinyl graft polymer 1 is a copolymer resin in which styrene, acrylonitrile, and butyl acrylate monomers are grafted to polyethylene, having a glass transition temperature (Tg) of 72° C.
The weight average molecular weight (Mw) of the binder resin is determined by subjecting THF solubles in the binder resin to a measurement by a gel permeation chromatographic apparatus GPC-150C (available from Waters Corporation) equipped with Shodex® Columns KF801-807 (available from Showa Denko K.K.) and a refractive index (RI) detector. The boiling point of ethyl acetate is 76.8° C.
Preparation of Toner
A toner is prepared from the above-obtained toner composition liquid using the toner manufacturing apparatus illustrated in
The toner composition liquid and the members of the toner manufacturing apparatus which contact the toner composition liquid are temperature-controlled to 55° C. The toner manufacturing apparatus is continuously operated for 6 hours without causing discharge hole clogging.
Toner Preparation Conditions
Longitudinal length (L) of liquid column resonance liquid chamber: 1.85 mm
Diameter of discharge hole outlet: 8.0 μm
Drying temperature (nitrogen): 60° C.
Drive frequency: 340 kHz
Applied voltage to piezoelectric body: 10.0 V
Next, 100 parts of the mother toner particles are mixed with commercially-available silica powders, i.e., 2.8 parts of NAX50 (from Nippon Aerosil Co., Ltd., having an average primary diameter of 30 nm) and 0.9 parts of H20TM (from Clariant, having an average primary diameter of 20 nm), using a HENSCHEL MIXER. The mixture is sieved with a mesh having an opening of 60 μm to remove coarse particles and aggregations. Thus, a toner 1 is prepared. The toner 1 is embedded in an epoxy resin and cut into ultrathin sections with an ultrasonic microtome.
After being dyed with RuO4, the ultrathin sections are observed with a transmission electron microscope (TEM).
The obtained image is analyzed using an image analysis software program ImageJ to determine average aspect ratio of the wax domain.
The number of the exothermic peak, the half bandwidth of the exothermic peak and the exothermic peak temperature are obtained from a differential scanning calorimetry (DSC) curve of cooling period.
The content of the wax is determined by converting the endothermic quantity of the toner 1 measured by a differential scanning calorimetry (DSC).
The amount of the wax existing in a region ranging from the surface to 0.3 μm in depth of the toner 1 is determined by an attenuated total reflection infrared spectroscopy (FTIR-ATR).
The particle size of the toner 1 is also measured.
The properties of the toner are shown in Table 2.
The procedure for preparation of the Toner 1 is repeated except for replacing materials shown in Table 2.
The vinyl graft polymer 2 is a copolymer resin in which styrene, acrylonitrile, and butyl acrylate monomers are grafted to polyethylene, having a glass transition temperature (Tg) of 65° C.
The vinyl graft polymer 3 is a copolymer resin in which styrene and butyl acrylate monomers are grafted to polyethylene, having a glass transition temperature (Tg) of 70° C.
Photographs of the toner obtained by a transmission electron microscope (TEM) in accordance with an Example 4 and 5 are similarly to Example 1 to 3.
The procedure in Example 1 is repeated except that the WAX 1 is replaced with a WAX 6 and ethyl acetate is replaced with toluene.
Thus, a toner 6 is prepared.
The WAX 6 is a paraffin wax having a melting point of 74.1° C. and a recrystallization temperature of 70.1° C. (from Nippon Seiro Co., Ltd.).
A Photograph of the toner obtained by a transmission electron microscope (TEM) in accordance with an Example 6 is similarly to Example 1 to 3.
The procedure in Example 1 is repeated except that the WAX 1 is replaced with a WAX 3, the amount of the polyester resin A is changed from 243.3 parts to 263.3 parts, and the amount of the vinyl graft polymer 1 is changed from 20 parts to 0 part.
Thus, a toner 7 is prepared.
The procedure in Comparative Example 1 is repeated except that the WAX 3 is replaced with a WAX 4.
Thus, a toner 8 is prepared.
A Photograph of the toner obtained by a transmission electron microscope (TEM) in accordance with a Comparative Example 2 is similarly to Comparative Example 1.
The procedure in Example 3 is repeated except the following procedure.
Preparation of Wax Dispersion Liquid
In a vessel equipped with stirrer blades and a thermometer, 20 parts of the WAX 3 and 80 parts of ethyl acetate are heated to 60° C. and stirred for 20 minutes to dissolve the WAX 3 in the ethyl acetate, followed by rapid cooling to precipitate fine particles of the WAX 3.
The resulting dispersion liquid is subjected to a dispersion treatment using a STAR MILL LMZ06 (from Ashizawa Finetech Ltd.) filled with zirconia beads having a diameter of 0.3 μm at a rotation speed of 1,800 rpm to more finely dispersed the wax.
Thus, a WAX 3 dispersion liquid, in which the average particle diameter is 0.3 μm and the maximum particle diameter is 0.8 μm, is prepared.
The particle size of the wax is measured by an instrument NPA-150 from Microtrac, Inc.
Preparation of Toner Composition Liquid
After dissolving 243.3 parts of the polyester resin A and 20 parts of a vinyl graft polymer 3 in 636.7 parts of ethyl acetate, 100 parts of the WAX 3 dispersion liquid and 100 parts of the carbon black dispersion liquid are mixed therein at 30° C. using a mixer having stirrer blades.
Thus, a toner composition liquid is prepared.
Preparation of Toner
A toner is prepared from the above-obtained toner composition liquid using the toner manufacturing apparatus illustrated in
The toner composition liquid and the members of the toner manufacturing apparatus which contact the toner composition liquid are temperature-controlled to 30° C. The toner manufacturing apparatus is continuously operated for 6 hours without causing discharge hole clogging.
Toner Preparation Conditions
Longitudinal length (L) of liquid column resonance liquid chamber: 1.85 mm
Diameter of discharge hole outlet: 8.0 μm
Drying temperature (nitrogen): 40° C.
Drive frequency: 340 kHz
Applied voltage to piezoelectric body: 10.0 V
The mother toner particles are mixed with external additives in the same manner as Example 1. Thus, a toner 9 is prepared. The properties of the toner are shown in Table 2.
The procedure in Comparative Example 3 is repeated except the following procedure.
Preparation of Toner Composition Liquid
After dissolving 263.3 parts of the polyester resin A in 636.7 parts of ethyl acetate, 100 parts of the WAX 3 dispersion liquid and 100 parts of the carbon black dispersion liquid are mixed therein at 30° C. using a mixer having stirrer blades.
Thus, a toner composition liquid is prepared.
Preparation of Toner
A toner is prepared from the above-obtained toner composition liquid using the toner manufacturing apparatus illustrated in
First, liquid droplets of the toner composition liquid are discharged.
The liquid droplets are dried and solidified by the liquid droplet solidification device using dry nitrogen.
The solidified particles are collected by a cyclone collector and fan-dried at 35° C., 90% RH for 48 hours and at 40°, 50% RH for 24 hours.
Thus, mother toner particles are obtained.
The toner composition liquid and the members of the toner manufacturing apparatus which contact the toner composition liquid are temperature-controlled to 30° C.
It is difficult to achieve stable continuous discharge because the wax settle out in the toner composition liquid and the discharge holes clog with the passage of time.
Toner Preparation Conditions
Longitudinal length (L) of liquid column resonance liquid chamber: 1.85 mm
Diameter of discharge hole outlet: 8.0 μm
Drying temperature (nitrogen): 40° C.
Drive frequency: 340 kHz
Applied voltage to piezoelectric body: 10.0 V
The mother toner particles are mixed with external additives in the same manner as Example 1.
Thus, a toner 10 is prepared.
The properties of the toner are shown in Table 2.
A Photograph of the toner obtained by a transmission electron microscope (TEM) in accordance with a Comparative Example 4 is similarly to Comparative Example 3.
Manufacture of Crystalline Resin A1
A reaction tank equipped with a cooling pipe, a stirrer, and a nitrogen introducing pipe is charged with a sebacic acid (303 parts), 1,6-hexanediol (230 parts), and titanium dihydroxy bis(triethanol aminate) (1.1 parts) as a condensation catalyst, and they are reacted under a nitrogen stream at 180° C. for 8 hours while distilling away produced water.
Then, while being gradually warmed to 220° C., they are reacted under a nitrogen stream for 4 hours while distilling away produced water and 1,6-hexanediol.
They are further reacted with pressure reduction of from 5 mmHg to 20 mmHg until the weight-average molecular weight reach 6,800, to thereby obtain a crystalline resin.
Next, the obtained crystalline resin is added to ethyl acetate (550 parts) and dissolved therein.
After this, a bisphenol A propylene oxide 2 mol adduct (33 parts), a bisphenol A ethylene oxide 2 mol adduct (20 parts), and 1,2-propanediol (8 parts) are added thereto and dissolve therein.
Then, 4,4′-diphenylmethane diisocyanate (MDI) (111 parts) is further added thereto, and the resultant is reacted under a nitrogen stream at 80° C. for 5 hours.
Then, the ethyl acetate is distilled away under a reduced pressure, to thereby obtain Crystalline Resin A1.
Manufacture of Colorant Master Batch P1
Crystalline Resin A1 (100 parts), a cyan pigment (C.I. Pigment blue 15:3) (100 parts), and ion-exchanged water (30 parts) are mixed well, and kneaded with an open roll kneader (KNEADEX manufactured by Nippon Coke & Engineering Co., Ltd.).
The kneading is started from a kneading temperature of 90° C., and after this, the temperature is gradually lowered to 50° C., to thereby manufacture Colorant Master Batch P1 in which the ratio between the resin and the colorant is 1:1 (mass ratio).
Manufacture of Wax Dispersion Liquid
A reaction vessel equipped with a cooling pipe, a thermometer, and a stirrer is charged with the WAX 6 (20 parts) and ethyl acetate (80 parts), and they are heated to 78° C. to be dissolved sufficiently, and then cooled to 30° C. in 1 hour while being stirred.
After this, the resultant is subjected to wet pulverization with ULTRA VISCOMILL (manufactured by Aimex Co., Ltd.) under the conditions of a liquid feeding rate of 1.0 kg/hr, a disk circumferential velocity of 10 m/sec., zirconia beads with a diameter of 0.5 mm being packed to 80% by volume, and 6 passes.
Ethyl acetate is added to the resultant to adjust the solid content concentration, to thereby manufacture Wax Dispersion Liquid with a solid content concentration of 20%.
Preparation of Oil Phase
A vessel equipped with a thermometer and a stirrer is charged with Crystalline Resin A1 (94 parts) and ethyl acetate (81 parts), and they are heated to the melting point of the resin or higher to be dissolved sufficiently.
Further, Wax Dispersion Liquid (25 parts) and Colorant Master Batch P1 (12 parts) are added thereto, and the resultant is stirred at 50° C. with TK HOMOMIXER (manufactured by Primix Corporation) at a rotation speed of 10,000 rpm to be dissolved and dispersed uniformly, to thereby obtain Oil Phase 1.
The temperature of Oil Phase 1 is maintained at 50 C in the vessel.
Preparation of Emulsified Slurry
Next, in another vessel equipped with a stirrer and a thermometer, ion-exchanged water (75 parts), a 25% dispersion liquid of organic resin particles for dispersion stabilization (copolymer of styrene-methacrylic acid-butyl acrylate-sodium salt of methacrylic acid ethylene oxide adduct sulfate) (manufactured by Sanyo Chemical Industries, Ltd.) (3 parts), carboxymethyl cellulose sodium (1 part), a 48.5% aqueous solution of dodecyldiphenyl ether disulfonic acid sodium (ELEMINOL MON-7 manufactured by Sanyo Chemical Industries, Ltd.) (16 parts), and ethyl acetate (5 parts) are mixed and stir at 40° C. to thereby manufacture Aqueous Phase Solution.
Oil Phase 1 (50 parts) maintained at 50° C. is added to the manufactured Aqueous Phase Solution, and they are mixed at 45° C. to 48° C. with TK HOMOMIXER (manufactured by Primix Corporation) at a rotation speed of 12,000 rpm for 1 minute, to thereby obtain Emulsified Slurry 1.
Emulsified Slurry 1 is poured in a vessel equipped with a stirrer and a thermometer, and desolventized at 50° C. for 2 hours, to thereby obtain Slurry 1.
The obtained Slurry 1 (100 parts) is filtered under a reduced pressure, and then washed as follows.
(1) ion-exchanged water (100 parts) is added to the filtration cake, followed by mixing with TK Homomixer (at a rotation speed of 6,000 rpm for 5 minutes) and then filtration;
(2) a 10% aqueous sodium hydroxide solution (100 parts) is added to the filtration cake obtained in (1), followed by mixing with TK Homomixer (at a rotation speed of 6,000 rpm for 10 minutes) and then filtration under reduced pressure;
(3) 10% hydrochloric acid (100 parts) is added to the filtration cake obtained in (2), followed by mixing with TK Homomixer (at a rotation speed of 6,000 rpm for 5 minutes) and then filtration;
and (4) ion-exchanged water (300 parts) is added to the filtration cake obtained in (3), followed by mixing with TK Homomixer (at a rotation speed of 6,000 rpm for 5 minutes) and then filtration. This process was repeated twice, to thereby obtain Filtration Cake 1.
The obtained Filtration Cake 1 is dried with an air-circulating drier at 45° C. for 48 hours, and then is caused to pass through a sieve with a mesh size of 75 μm, to thereby prepare mother toner particles.
The mother toner particles are mixed with external additives in the same manner as Example 1.
Thus, a toner 11 is prepared.
The properties of the toner are shown in Table 2.
A Photograph of the toner obtained by a transmission electron microscope (TEM) in accordance with a Comparative Example 5 is similarly to Comparative Example 3.
Preparation of Carrier
A mixture of 100 parts of a silicone resin (organo straight silicone), 100 parts of toluene, 5 parts of γ-(2-aminoethyl)aminopropyl trimethoxysilane, and 10 parts of a carbon black is subjected to a dispersion treatment for 20 minutes using a HOMOMIXER to prepare a coating layer forming liquid. The coating layer forming liquid is applied to the surfaces of 1,000 parts of spherical magnetite particles having a particle diameter of 50 μm using a fluidized-bed coating device. Thus, a magnetic carrier is prepared.
Preparation of Two-Component Developer
Each of the above prepared toners 1 to 11 in an amount of 4 parts is mixed with the magnetic carrier in an amount of 96.0 parts using a ball mill.
Thus, two-component developers 1 to 11 are prepared.
Each of the two-component developers 1 to 11 is subjected to the evaluation of cold offset resistance, charge stability with time, environmental charge stability and image stability as follows.
The evaluation results are shown in Table 3.
Particle Size of Toner
The weight average particle diameter (Dv) and number average particle diameter (Dn) of toner can be measured by a particle size analyzer MULTISIZER III (from Beckman Coulter, Inc.) with setting the aperture diameter to 50 μm. The volume and number of toner particles are measured first, and then the volume distribution and number distribution are calculated. The volume average particle diameter (Dv) and number average particle diameter (Dn) are determined from the volume distribution and number distribution, respectively. The ratio (Dv/Dn) of the volume average particle diameter (Dv) to the number average particle diameter (Dn) can be used as an indicator of particle size distribution. When the particle size distribution is monodisperse, the ratio (Dv/Dn) becomes 1. The greater the ratio (Dv/Dn), the wider the particle size distribution.
Cold Offset Resistance
Each of the developers is set in a commercially-available copier IMAGIO NEO C600 (from Ricoh Co., Ltd.).
A rectangular image having a size of 3 cm×5 cm is formed on an A4-size paper sheet (T6000 70W machine direction, from Ricoh Co., Ltd.) at a position 5 cm away from the leading edge of the sheet with a toner deposition amount of 0.85 mg/cm2.
The image is fixed on the sheet while controlling the fixing member to have a temperature of 130° C. and a linear speed of 300 mm/sec.
The toner deposition amount is calculated from the weight difference of the sheet before and after the image formation.
The image is visually observed to determine whether offset has occurred or not at 130° C., and cold offset resistance is evaluated based on the following criteria.
AA: Cold offset has not occurred.
A: The number of portions where cold offset has slightly occurred is 3 or less.
B: The number of portions where cold offset has slightly occurred is greater than 3.
C: Cold offset has occurred.
Charge Stability with Time
Each of the developers is set in a tandem color image forming apparatus IMAGIO NEO C600 (from Ricoh Co., Ltd.).
A running test in which an image chart having an image area ratio of 20% is continuously printed on 200,000 paper sheets is conducted while controlling the toner density such that the image density is kept at 1.4±0.2.
Charge stability is evaluated in terms of the amount of change in charge quantity (μC/g) of the developer before and after the running test, i.e., the ratio of the amount of decrease in charge quantity after the running test to the initial charge quantity, based on the following criteria.
The charge quantity is measured by a blow off method.
AA: less than 15%
A: 15% or more and less than 30%
B: 30% or more and less than 50%
C: 50% or more
The charge quantity is decreased as the toner is adhered to the carrier or the toner itself deteriorates.
The smaller the amount of change in charge quantity before and after the running test, the smaller the degree of toner filming on the carrier.
Environmental Charge Stability
Each developer is conditioned at 10° C. for 90 min in 15% RH (i.e., L/L environment). Thereafter, Each developer is agitated in a polypropylene container for 1 minute. Thereafter, The charge quantity of each developer is measured by a blow off method.
The same procedure is repeated at 30° C. in 90% RH (i.e., H/H environment)
The variation rate is determined from the following formula.
Variation rate (%)=(Q/M(LL)−Q/M(HH))/(A mean value of Q/M(LL) and Q/M(HH))×100
Wherein Q/M(LL) and Q/M(HH) represent charge amounts in L/L and H/H environments, respectively.
The variation rate is graded as follows.
AA: less than 50%
A: 50% or more and less than 70%
B: 70% or more and less than 90%
C: 90% or more
Image Stability
Each of the developers is set in a commercially-available copier IMAGIO NEO 455 (from Ricoh Co., Ltd.). A running test in which an image chart having an image area ratio of 7% is continuously printed on 50,000 sheets of a paper TYPE 6000 (from Ricoh Co., Ltd.) is conducted. Image stability is evaluated in terms of image quality (i.e., image density and thin-line reproducibility) of the 50,000th image based on the following criteria.
A: The 50,000th image is equivalent to the initial image in terms of image quality.
B: The 50,000th image has been changed from the initial image in terms of image quality and/or thin-line reproducibility with acceptable level.
C: The 50,000th image has been significantly changed from the initial image in terms of image quality and/or thin-line reproducibility, which is beyond the acceptable level.
Evaluation of One-Component Developer
Each of the toners 1 to 11, as a one-component developer, is subjected to the evaluation of cold offset resistance, adherence resistance, charge stability with time, environmental charge stability, and image stability as follows.
The evaluation results are shown in Table 3.
Cold Offset Resistance
Each of the developer is set in a modified machine of IPSIO SP C220 (from Ricoh Co., Ltd.) which has been modified such that the temperature of the fixing roller is variable. A solid image having a toner deposition amount of 1.00±0.05 mg/cm2 is formed on a sheet of a paper TYPE 6200 (from Ricoh Co., Ltd.).
The solid image is fixed on the sheet while controlling the fixing roller to have a temperature of 140° C. The fixed image is visually observed to determine whether offset has occurred or not at 140° C., and cold offset resistance is evaluated based on the following criteria.
AA: Cold offset has not occurred.
A: The number of portions where cold offset has slightly occurred is 3 or less.
B: The number of portions where cold offset has slightly occurred is greater than 3.
C: Cold offset has occurred.
Charge Stability with Time
Each of the developers is set in an image forming apparatus IPSiO SP C220 (from Ricoh Co., Ltd.).
A running test in which an image chart having an image area ratio of 20% is continuously printed on 200,00 paper sheets is conducted while controlling the toner density such that the image density is kept at 1.4±0.2.
Charge stability is evaluated in terms of the amount of change in charge quantity (μC/g) of the developer before and after the running test, i.e., the ratio of the amount of decrease in charge quantity after the running test to the initial charge quantity, based on the following criteria.
The charge quantity is measured by a suck in method.
Evaluation Criteria
AA: less than 15%
A: 15% or more and less than 30%
B: 30% or more and less than 50%
C: 50% or more
Environmental Charge Stability
Each developer is conditioned at 10° C. for 90 min in 15% RH (i.e., L/L environment). Thereafter, each developer is set in an image forming apparatus IPSiO SP C220 (from Ricoh Co., Ltd.).
A running test in which an image chart having an image area ratio of 20% is continuously printed on 100 paper sheets is conducted while controlling the toner density such that the image density is kept at 1.4±0.2.
The charge quantity (μC/g) of the developer after the running test is measured by a suck in method.
The same procedure is repeated at 30° C. in 90% RH (i.e., H/H environment)
The variation rate is determined from the following formula.
Variation rate (%)=(Q/M(LL)−Q/M(HH))/(A mean value of Q/M(LL) and Q/M(HH))×100
Wherein Q/M(LL) and Q/M(HH) represent charge amounts in L/L and H/H environments, respectively.
The variation rate is graded as follows.
AA: less than 50%
A: 50% or more and less than 70%
B: 70% or more and less than 90%
C: 90% or more
Image Stability
Each of the developer is set in IPSiO SP C220 (from Ricoh Co., Ltd.).
A black solid image is printed on a sheet of a paper TYPE 6000 (from Ricoh Co., Ltd.) before and after a running test in which an image chart having an image area ratio of 1% is continuously printed on 2,000 paper sheets.
The image density of each black solid image is measured with a spectrophotometer (from X-Rite).
Image stability is evaluated in terms of the difference in image density of the black solid image before and after the running test based on the following criteria.
AA: The difference in image density is less than 0.1%.
A: The difference in image density is 0.1% or more and less than 0.2%.
B: The difference in image density is 0.2% or more and less than 0.3%.
C: The difference in image density is 0.3% or more.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2014-186581 | Sep 2014 | JP | national |
