JP2010204138A - Image forming toner, single-component developer, two-component developer, image forming method using the toner, image forming apparatus and process cartridge - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide pulverized toner (image forming toner), uniformly dispersing a pigment in toner while achieving high-temperature offset, high glossiness and fixing lower limit temperature, and having high saturation and a wide offset band. <P>SOLUTION: The pulverized toner (image forming toner) at least contains a colorant and binder resin. The binder resin has an unsaturated bond. When a pigment dispersant where a crosslinking initiator is dissolved or dispersed is added to the binder resin, and molten and kneaded, the unsaturated bond forms a crosslinking point. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

  The present invention relates to an image forming toner, and more specifically, an image forming toner used in an image forming apparatus using an electrophotographic method such as an electrostatic copying machine or a laser beam printer, and a one-component developer or the like The present invention relates to a two-component developer, and an image forming method, an image forming apparatus, and a process cartridge using the image forming toner.

  Since the number of output sheets per unit time required for the image forming apparatus is increasing year by year, further speeding is desired. As this speed increases, technically more severe conditions are required. In particular, in recent years when electrophotographic systems are being used for on-demand digital printing, it is necessary to further widen the temperature range in which no offset occurs while maintaining high gloss.

  However, the thermal energy per unit time (nip time) that can be supplied to the image forming toner (hereinafter sometimes simply referred to as “toner”) as the speed increases, The amount of energy that can be applied cannot be increased, so it is less than before. Accordingly, sufficient heat is not transmitted to the image forming toner, and the image forming toner existing on or near the surface of the recording medium is poorly melted.

  When toner fusing failure occurs during fixing, the toner layer on the recording medium is cut due to insufficient viscosity at the location where fusing failure occurs, one remains on the recording medium and the other adheres to the fixing roller. End up. Alternatively, since the melting defect occurs, the adhesion force between the recording medium and the toner is insufficient, and all the toner on the recording medium adheres (offsets) to the fixing roller. As in the case of the offset described above, the toner adhering to the fixing roller is fixed to a place other than the desired location of the recording medium that is transported next, causing a ghost image or the like. That is, when the heating is not sufficient, an offset phenomenon, a so-called cold offset phenomenon occurs, which is a problem.

  In addition, poor melting of the toner at the time of fixing has been a problem because even if the cold offset phenomenon does not occur, it causes the image quality of the output image to deteriorate, such as the glossiness being significantly reduced.

Therefore, in order to solve these problems related to poor melting, research and development of toners containing resins, mold release agents, fixing aids, etc. with a low softening point (melting point) for the purpose of fixing at lower temperatures. Has been made energetically.
For example, the inventors of the present invention first focused on the endothermic peak of the toner, and defined the difference between the endothermic peak of the toner before heat treatment of the toner and after storage for 72 hours at 40 ° C. (for example, Patent Document 1). Or the FTIR spectral ratio of the crystalline polyester resin before and after storage at a constant temperature of 45 ° C. for 12 hours (see, for example, Patent Document 2) ) Proposed a method to improve the low-temperature fixability, heat-resistant storage stability, and offset resistance of the toner.
Further, the dispersion diameter of the colorant and the dispersion diameter of the release agent in the binder resin are respectively defined, and the charge amount of the toner (charge rising ratio: normal temperature and humidity, toner concentration 5%) When the charge amount obtained when stirring and mixing for 20 seconds under the same conditions is Q ₂₀ with respect to the charge amount Q ₆₀₀ obtained when stirring and mixing for a minute, Z (%) = (Q ₂₀ / Q ₆₀₀ ) × 100 The method of improving color reproducibility, offset resistance and charge rise characteristics at a high image density of the toner has been proposed (for example, see Patent Document 3).

  However, a toner excellent in low-temperature fixability generally has a problem relating to heat-resistant storage stability, in which the storage stability in a high-temperature environment is reduced and solidified. That is, in the toner, there is a trade-off relationship between low-temperature fixability and heat-resistant storage stability. In other words, as the speed of image forming apparatuses increases, it is required to fix the toner with lower thermal energy. However, the toner having excellent low-temperature fixability does not have sufficient heat-resistant storage stability in a high-temperature environment. It becomes a difficult problem in handling during storage and transportation. In contrast, a toner having excellent heat-resistant storage stability does not have sufficient low-temperature fixability, and causes image quality problems such as a cold offset phenomenon.

  Therefore, in a pulverized toner including a melting / kneading step, two or more types of resins having different molecular weights or rheologies are heated and kneaded, and for fixing at low temperature, the low molecular weight resin is melted to form a base material (recording medium). By providing a fixing property and preventing the offset to the fixing member with a high molecular weight or high elasticity / high viscosity resin for the fixing property at a high temperature, the fixing separation is prevented without causing any adhesion or offset to the fixing roller at a low temperature and a high temperature. A method of widening the temperature range in which the mold can be used is widely and generally performed (see, for example, Patent Document 4).

However, when trying to melt and knead two or more types of resins that have significantly different molecular weights or rheology because they are trying to widen the temperature range that can be fixed, shearing force is applied to the resin due to the difference in viscosity between the two. Phenomenon that is not uniformly dispersed. In this case, not only the high viscosity portion and the low viscosity portion are observed as a sea island structure, but also the dispersibility of the pigment, the release agent, or the charge control agent is remarkably lowered. This is a factor that degrades the performance of the machine, such as image unevenness and fogging, particularly a reduction in image quality (image saturation).
This is particularly because less heat energy can be applied per unit time, and in high-speed machines with high voice demands for higher image quality, the decrease in saturation appears as a more noticeable image defect, and the use of pulverized toner In some cases, it was an important issue that had to be solved quickly.

  An object of the present invention is to provide a pulverized toner having both high temperature offset, high gloss, and minimum fixing temperature, uniform pigment dispersion in the toner, high chroma and a wide offset band. Another object of the present invention is to provide a one-component developer or two-component developer using the toner, and an image forming method, an image forming apparatus, and a process cartridge using the image forming toner.

  As a result of intensive studies on image forming toners, the present inventors have found that the above problems can be solved by the following method. Specifically, in order to solve the above-described problems, the image forming toner, the one-component developer, the two-component developer, the image forming method, the image forming apparatus, or the process cartridge using the toner according to the present invention are specifically described. It has the technical features described in the following (1) to (13).

(1) A pulverized toner containing at least a colorant and a binder resin, wherein the binder resin has an unsaturated bond, and a pigment dispersant in which a crosslinking initiator is dissolved or dispersed is added and melt kneaded. The toner for image formation, wherein the unsaturated bond forms a crosslinking point.
(2) The image forming toner as described in (1) above, wherein the binder resin contains a polyester resin as a main component.
(3) The image forming toner according to (1) or (2) above, wherein the amount of the pigment dispersant added is 1 to 5 parts by weight with respect to 100 parts by weight of the binder resin.
(4) The electrophotographic toner according to any one of (1) to (3) above, wherein the pigment dispersant has a weight average molecular weight of 400 to 3000.
(5) The toner for image formation as described in any one of (1) to (4) above, wherein the toner has a weight average molecular weight of 18000 or more.
(6) The toner for image formation as described in any one of (1) to (5) above, wherein the toner has a weight average particle diameter of 3.5 μm to 10 μm.

(7) A one-component developer comprising the image forming toner according to any one of (1) to (6).
(8) A two-component developer comprising the image forming toner according to any one of (1) to (6) and a carrier.

(9) A charging step for charging at least the surface of the image carrier, an electrostatic latent image forming step for forming an electrostatic latent image on the image carrier, and developing the electrostatic latent image using image forming toner. A developing step for forming a visible image, a transfer step for transferring the visible image onto a recording medium to form an unfixed image, and a fixing step for fixing the unfixed image on the recording medium. An image forming method comprising: an image forming toner according to any one of (1) to (6) above, wherein the image forming toner used to form the visible image is Forming method.
(10) The image forming method as described in (9) above, wherein the conveyance speed of the recording medium in the fixing step is 280 mm / second or more.

(11) At least an image carrier, a charging unit that charges the surface of the image carrier, an exposure unit that exposes the charged image carrier surface to form an electrostatic latent image, and the electrostatic latent image Developing means for forming a visible image by developing with toner for forming an image; transfer means for transferring the developed toner image onto a recording medium to form an unfixed image; and An image forming apparatus comprising: a fixing unit configured to fix the recording medium, wherein the image forming toner used to form the visible image is any one of (1) to (6). An image forming apparatus comprising a toner for forming.
(12) The image forming apparatus according to (11), wherein a conveyance speed of the recording medium at the time of fixing by the fixing unit is 280 mm / second or more.

(13) An image carrier, charging means for charging the surface of the image carrier, exposure means for exposing the charged surface of the image carrier to form an electrostatic latent image, and forming an image on the formed electrostatic latent image At least one means selected from developing means for developing using the forming toner, transfer means for transferring the developed toner image to the recording medium, and cleaning means for removing the toner remaining on the surface of the image carrier after transfer. A process cartridge that can be attached to and detached from an integrated image forming apparatus main body, wherein the image forming toner to be used is the image forming toner according to any one of (1) to (6) above. Process cartridge.

  According to the toner of the present invention and its one-component developer and two-component developer, an offset phenomenon (cold offset and hot offset) does not occur even at a high-speed output in an electrophotographic image forming apparatus. In addition to being fixed only at the position and having excellent low-temperature fixability and heat-resistant storage stability, high-quality image output is possible.

  According to the image forming method of the present invention, since the image forming toner having excellent low-temperature fixability and offset resistance is used, even if an image is formed by an electrophotographic image forming apparatus having a high output, ghosting or the like occurs. High-quality images can be output stably.

According to the image forming apparatus of the present invention, since the image forming toner having both the low temperature fixing property and the heat resistant storage stability and having the excellent glossiness and offset resistance is used, an abnormal image is generated even if the process linear velocity is high. And a stable image with high image quality can be output.
The image forming method and the image forming apparatus of the present invention can be widely applied to electrophotographic application fields using electrophotography (for example, electrostatic copying machines, laser beam printers, etc.).

  Further, according to the process cartridge of the present invention, since the toner of the present invention is supplied from the developing unit, the fixing unit stably fixes only at a desired position on the recording medium without causing an offset phenomenon due to an unfixed image. In addition, a higher quality image can be output. In addition, maintenance management and handling are easy.

It is a schematic block diagram which shows an example of the image forming apparatus used for implementation of the image forming method of this invention. It is a schematic block diagram which shows the other example of the image forming apparatus used for implementation of the image forming method of this invention. It is a schematic block diagram which shows the example of the tandem type color image forming apparatus used for implementation of the image forming method of this invention. FIG. 5 is a partially enlarged schematic configuration diagram of the image forming apparatus illustrated in FIG. 4. It is a schematic block diagram which shows an example of the process cartridge of this invention. 3 is a diagram illustrating a pigment dispersion state of the image forming toner 1 obtained in Example 1. FIG. 6 is a diagram illustrating a pigment dispersion state of an image forming toner 14 obtained in Comparative Example 3. FIG.

  Details of the present invention will be described below, but the present invention is not limited thereto.

(Uniform dispersion of molecular weight components with different rheology)
When two or more kinds of resins having greatly different rheology are used, the pigment is unevenly distributed in the resin used in the masterbatch and a resin having a rheology close to that, so that a portion where the pigment exists and a portion where the pigment does not exist are formed in the toner.
In such a case, compared to the case where the pigment is uniformly dispersed in the toner, the absorption intensity of visible light is lowered, so that the saturation is also lowered and the vividness of the image is lost, resulting in poor image quality. Cause.

  However, by previously dissolving or dispersing a crosslinking initiator dispersed in a pigment dispersant in a resin having a possibility of having a crosslinking point, an intermolecular crosslinking point can be uniformly generated in the resin.

The mechanism that can generate a crosslinking point in the same resin with high uniformity has not yet been clarified, but is considered as follows.
That is, a general pigment dispersant has a high affinity with the pigment and the resin and is uniformly dispersed in the resin. Even if it is a material that is difficult to disperse by itself, the crosslinking initiator is uniformly dispersed by the effect of the pigment dispersing agent by the pigment dispersing agent in which the crosslinking initiator is dispersed.
On the other hand, since molecules having an unsaturated bond capable of causing a crosslinking reaction are uniformly present in the resin, it is considered that the crosslinking points are also uniformly generated by the uniformly dispersed crosslinking initiator. By this effect, it is possible to uniformly generate a portion having a high molecular weight due to a crosslinking point and a low molecular weight portion having no crosslinking. Furthermore, since the pigment dispersant is also present in the portion where the crosslinking point is generated, the uniform presence of the pigment can be realized.
From the above, it is possible for the high molecular weight component and the low molecular weight component to be uniformly present in the same resin, and it is possible to further increase the dispersion of the pigment.

(Concentration of crosslinking initiator contained in pigment dispersant)
The concentration of the crosslinking initiator contained in the pigment dispersant and the concentration relative to the resin can be designed under various conditions depending on the desired physical properties of the resin. An example of the best mode will be described below, but these conditions do not limit the present invention.

  The amount of the crosslinking initiator is preferably 0.1 to 100 parts by weight with respect to 100 parts by weight of the pigment dispersant. When the amount of the crosslinking initiator is less than this, the crosslinking reaction does not proceed and the polymer component cannot be formed. In addition, when the amount of the crosslinking initiator contained is larger than this, the speed of the crosslinking reaction is increased, unevenness occurs at the crosslinking points, and the polymer component cannot be formed uniformly. The above conditions are appropriate for obtaining a good image.

  On the other hand, the amount of the crosslinking initiator is preferably 0.01 to 3 parts by weight with respect to 100 parts by weight of the binder resin. When the crosslinking initiator is less than this, the crosslinking reaction does not proceed, the polymer component cannot be formed, and both hot offset and low temperature fixability cannot be achieved. On the other hand, when the amount of the crosslinking initiator contained is larger than this, the crosslinking reaction proceeds excessively, resulting in high elasticity, low-temperature fixability being impaired, and further obtaining a low gloss image. The above conditions are appropriate for obtaining a good image.

  The amount of the pigment dispersant is preferably 1 to 5 parts by weight with respect to 100 parts by weight of the binder resin, and preferably 1 to 50 parts by weight with respect to 100 parts by weight of the pigment. When the amount of the pigment dispersant is less than this, the effect on the pigment dispersion cannot be obtained, and the possibility of the aggregation of the pigment increases. In addition, when there are more pigment dispersants than this, the effect of plasticizing the resin often appears, and in particular, there is a risk of gloss reduction and image failure due to the occurrence of hot offset during high-temperature fixing. The above conditions are appropriate for obtaining a good image.

(Crosslinking initiator)
As the crosslinking initiator used in the present invention, all known radical reactants can be used. Examples of the organic peroxide include benzoyl peroxide, di-t-butyl peroxide, and t-butylcumyl peroxide. , Dicumyl peroxide, α, α-bis (t-butylperoxy) diisopropylbenzene, 2,5-dimethyl-2,5-bis (t-butylperoxy) hexane, di-t-hexyl peroxide 2,5-dimethyl-2,5-di-t-butylperoxyhexine-3, acetyl peroxide, isobutyryl peroxide, octaninnor peroxide, decanolyl peroxide, lauroyl peroxide, 3, 3, 5-trimethylhexanoyl peroxide, m-toluyl peroxide, t-butylperoxyisobutyrate, t-butyl Ruperoxyneodecanoate, cumylperoxyneodecanoate, t-butylperoxy-2-ethylhexanoate, t-butylperoxy3,5,5-trimethylhexanoate, t-butylperoxylaur Rate, t-butyl peroxybenzoate, t-butyl peroxyisopropyl carbonate, t-butyl peroxyacetate and the like.

(Pigment dispersant)
The pigment dispersant used in the present invention is preferably highly compatible with the binder resin in terms of pigment dispersibility. Specific commercial products such as “Azisper PB821” and “Azisper PB822” The BYK-P series and Disperbyk series manufactured by BYK Chemie, including the Ajisper series (manufactured by Ajinomoto Fine Techno Co., Ltd.) and “Disperbyk-2001”, and “EFKA-4010” manufactured by EFKA, etc. Resins having a composition similar to that used for the binder resin, fatty acids such as stearic acid, and esters thereof reacted with various alcohols can also be used. Although the material which esterified glycerin and stearic acid is used for the Example, this invention is not limited to the material at all.

  The weight average molecular weight of the pigment dispersant is the molecular weight of the maximum value of the main peak in terms of styrene in GPC, preferably 400 to 3000, and particularly preferably 600 to 1000 from the viewpoint of pigment dispersibility. When the molecular weight is less than 400, the polarity becomes high and the dispersibility of the colorant may be reduced or cause hot offset. When the molecular weight exceeds 3000, the affinity with the solvent becomes high, and the colorant. The dispersibility of the resin may decrease. Moreover, the polyester resin which has these molecular weights can also be used as a dispersing agent.

(Mixture of pigment dispersant and crosslinking initiator)
For mixing the pigment dispersant and the crosslinking initiator, all known kneaders can be used. For example, a continuous twin screw extruder (for example, KTK type twin screw extruder manufactured by Kobe Steel, TEM manufactured by Toshiba Machine Co., Ltd.). Type twin screw extruder, Ikegai Iron Works Co., Ltd. PCM type twin screw extruder, Kurimoto Iron Works Co., Ltd. KEX type twin screw extruder), continuous single screw kneader (for example, Buses Co. Kneader, KCK Corporation) Thermal kneaders such as a kneading machine) and a direct open roll type continuous kneader needex (open roll continuous kneading granulator, manufactured by Mitsui Mining Co., Ltd.) can be used.

(Binder resin that can be used in the present invention)
As the resin having an unsaturated bond in the molecule used in the present invention, all resins conventionally used for image forming toners can be used. For example, homopolymers of styrene such as polystyrene, polychlorostyrene, and polyvinyltoluene, and substituted products thereof; styrene / p-chlorostyrene copolymer, styrene / propylene copolymer, styrene / vinyltoluene copolymer, styrene / vinyl Naphthalene 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 / α-chloromethyl methacrylate copolymer, styrene / acrylonitrile copolymer, styrene / vinyl ethyl ether copolymer, styrene / vinyl methyl Ketone copolymer, steel Styrene copolymers such as styrene / butadiene copolymer, styrene / isoprene copolymer, styrene / acrylonitrile / indene copolymer, styrene / maleic acid copolymer, styrene / maleic acid ester copolymer; polymethyl methacrylate , Polybutyl methacrylate, polyvinyl chloride, polyvinyl acetate, polyethylene, polypropylene, polyester, polyvinyl butyl butyral, polyacrylic acid resin, rosin, modified rosin, terpene resin, phenol resin, aliphatic or alicyclic hydrocarbon resin, aromatic A group petroleum resin, chlorinated paraffin, paraffin wax and the like can be mentioned, and these are used alone or in admixture of two or more.

In the toner according to the present invention, among the enumerated above, it is preferable to use a polyester resin as a binder resin because of excellent low-temperature fixability.
In addition, since the image needs to be glossy, the molecular weight of the binder resin is relatively small. In the case of a polyester resin, the resin strength can be easily obtained even if the molecular weight is small, and the toner is finely pulverized while stirring the toner. It is less likely to aggregate or agglomerate, and is more advantageous than a general vinyl polymer resin for toner.

Moreover, as a monomer which comprises a polyester resin, although not limited, the following are mentioned. It should be noted that the following alcohol and acid-modified monomers obtained by dehydrogenating appropriate functional group portions so as to have desired physical properties can be used for the purpose of providing crosslinking points in the resin.
Specifically, as the divalent alcohol component, for example, ethylene glycol, propylene glycol, 1,3-butanediol, 1,4-butanediol, 2,3-butanediol, diethylene glycol, triethylene glycol, 1,5 -Obtained by polymerization of cyclic ethers such as ethylene oxide and propylene oxide on pentanediol, 1,6-hexanediol, neopentyl glycol, 2-ethyl-1,3-hexanediol, hydrogenated bisphenol A, or bisphenol A Diols, and the like.

  In order to crosslink the polyester resin, it is preferable to use a trivalent or higher alcohol together. Examples of the trihydric or higher polyhydric alcohol include sorbitol, 1,2,3,6-hexanetetrol, 1,4-sorbitan, pentaerythritol, such as dipentaerythritol, tripentaerythritol, 1,2,4- Butanetriol, 1,2,5-pentatriol, glycerol, 2-methylpropanetriol, 2-methyl-1,2,4-butanetriol, trimethylolethane, trimethylolpropane, 1,3,5-trihydroxybenzene , Etc.

  Examples of acid components that form polyester polymers include benzene dicarboxylic acids such as phthalic acid, isophthalic acid, and terephthalic acid, or anhydrides thereof, alkyl dicarboxylic acids such as succinic acid, adipic acid, sebacic acid, and azelaic acid, or the like. Unsaturated dibasic acids such as anhydride, maleic acid, citraconic acid, itaconic acid, alkenyl succinic acid, fumaric acid, mesaconic acid, maleic anhydride, citraconic anhydride, itaconic anhydride, alkenyl succinic anhydride, etc. Unsaturated dibasic acid anhydrides, and the like.

  Trivalent or higher polyvalent carboxylic acid components include trimet acid, pyrometic 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-dicarboxy-2-methyl-2-methylenecarboxypropane, tetra (methylenecarboxy ) Methane, 1,2,7,8-octanetetracarboxylic acid, emporic trimer acid, or their anhydrides, partially lower alkyl esters, and the like.

(Glass transition temperature (Tg) of resin used)
The glass transition temperature (Tg) of the polyester resin preferably used in the present invention is desirably low as long as the heat resistant storage stability of the toner is not deteriorated. In general, the Tg is 40 to 70 ° C., preferably 60 to 70 ° C. 65 ° C. When Tg is higher than the above range, the lower limit fixing temperature of the toner is increased, so that the low temperature fixing property of the toner is deteriorated.
The glass transition temperature (Tg) can be measured using a TG-DSC system (TAS-100) manufactured by Rigaku Corporation in the same manner as the Tg of the toner described later.

(Molecular weight of the resin used)
In the image forming toner of the present invention, in order to achieve both low-temperature fixability and heat-resistant storage stability and appropriate gloss (glossiness), the weight average molecular weight (Mw) of the resin (for example, polyester resin) in the toner is 1000. It is desirable to be about ˜500000. Note that the number average molecular weight (Mn) may be measured instead of the weight average molecular weight.
The weight average molecular weight (Mw) or the number average molecular weight (Mn) can be measured as follows.

[Measurement of weight average molecular weight (Mw)]
The mass average molecular weight of the binder resin is measured by GPC (gel permeation chromatography) under the following conditions.
・ Apparatus: GPC-150C (manufactured by Waters)
Column: KF801-807 (manufactured by Shodex)
・ Temperature: 40 ℃
・ Solvent: THF (tetrahydrofuran)
・ Flow rate: 1.0 mL / min ・ Sample: 0.1 mL injection of a sample with a concentration of 0.05 to 0.6% Molecular weight created from a monodisperse polystyrene standard sample from the molecular weight distribution of the binder resin measured under the above conditions The mass average molecular weight of the binder resin is calculated using the calibration curve.

[Measurement of Number Average Molecular Weight (Mn)]
The number average molecular weight of the binder resin is measured by GPC under the following conditions.
・ Apparatus: GPC-150C (manufactured by Waters)
Column: KF801-807 (manufactured by Shodex)
・ Temperature: 40 ℃
・ Solvent: THF (tetrahydrofuran)
Flow rate: 1.0 mL / min Sample: Inject 0.1 mL of a sample having a concentration of 0.05 to 0.6%.
Further, when the insoluble content when 1 g of a sample (binder resin) is added to 100 ml of THF is 75% by weight or more, DMF (dimethylformamide) is used as a solvent. The number average molecular weight is calculated from a molecular weight calibration curve prepared using a monodisperse polystyrene standard sample.

(Coloring agent)
As the colorant used in the image forming toner of the present invention, all known dyes and pigments can be used.
For example, carbon black, nigrosine dye, iron black, naphthol yellow S, Hansa yellow (10G, 5G, G), cadmium yellow, yellow iron oxide, ocher, yellow lead, titanium yellow, polyazo yellow, oil yellow, Hansa Yellow (GR, A, RN, R), Pigment Yellow L, Benzidine Yellow (G, GR), Permanent Yellow (NCG), Vulcan Fast Yellow (5G, R), Tartrazine Lake, Quinoline Yellow Lake, Anthrazan Yellow BGL , Isoindolinone yellow, bengara, red lead, red lead, cadmium red, cadmium mercury red, antimony red, permanent red 4R, para red, phise red, parachlor ortho nitroaniline red, risor fast scarlet G, Reliant Fast Scarlet, Brilliant Carmin BS, Permanent Red (F2R, F4R, FRL, FRLL, F4RH), Fast Scarlet VD, Belkan Fast Rubin B, Brilliant Scarlet G, Resol Rubin GX, Permanent Red F5R, Brilliant Carmine 6B, Pogment 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, Alizarin Lake, Thioindigo Red B, Thioindigo Maroon, oil red, quinacridone red, pyrazolone red, polyazo red, chrome vermilion, benzidine Range, Perinone Orange, Oil Orange, Cobalt Blue, Cerulean Blue, Alkaline Blue Lake, Peacock Blue Lake, Victoria Blue Lake, Metal Free Phthalocyanine Blue, Phthalocyanine Blue, Fast Sky Blue, Indanthrene Blue (RS, BC), Indigo , Ultramarine, bitumen, anthraquinone blue, fast violet B, methyl violet lake, cobalt purple, manganese purple, dioxane violet, anthraquinone violet, chrome green, zinc green, chromium oxide, pyridiane, emerald green, pigment green B, naphthol green B, Green Gold, Acid Green Lake, Malachite Green Lake, Phthalocyanine Green, Anthraquinone Green, Oxidized Chi Tan, zinc white, litbon and mixtures thereof.
The content of the colorant is usually 1 to 15% by weight, preferably 3 to 10% by weight, based on the image forming toner.

  The colorant may be used as a master batch combined with a resin. The resin is not particularly limited and may be appropriately selected from known ones according to the purpose. For example, styrene or a substituted polymer thereof, a styrene 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 hydrocarbon resin, alicyclic ring Aromatic hydrocarbon resin, aromatic petroleum resin, chlorinated paraffin, paraffin, and the like. These may be used individually by 1 type and may use 2 or more types together.

  Examples of the polymer of styrene or a substituted product thereof include polyester resin, polystyrene, poly p-chlorostyrene, polyvinyl toluene, and the like. Examples of the styrene copolymer include a styrene-p-chlorostyrene copolymer, a styrene-propylene copolymer, a styrene-vinyltoluene copolymer, a styrene-vinylnaphthalene copolymer, and a styrene-methyl acrylate copolymer. Polymer, 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-p-chloromethyl methacrylate copolymer, styrene-acrylonitrile copolymer, styrene-vinyl methyl ketone copolymer, styrene-butadiene copolymer, styrene-isoprene copolymer, styrene An acrylonitrile-indene copolymer, Styrene - maleic acid copolymer, styrene - maleic acid ester copolymer, and the like.

  The masterbatch can be manufactured by mixing or kneading the resin for compounding for the masterbatch and the colorant under high shear. At this time, it is preferable to add an organic solvent in order to enhance the interaction between the colorant and the resin. Also, the so-called flushing method is preferable in that the wet cake of the colorant can be used as it is, and there is no need to dry it. This flushing method is a method in which an aqueous paste containing colorant water is mixed or kneaded together with a resin and an organic solvent, and the colorant is transferred to the resin side to remove (reduce) moisture and the organic solvent. For the mixing or kneading, for example, a high shear dispersion device such as a three-roll mill is preferably used.

  The image forming toner according to the present invention may contain a release agent, a charge control agent, an external additive, and the like as required, as long as the effects of the present invention are not impaired.

(Release agent)
There is no restriction | limiting in particular as a mold release agent used for the toner for image formation of this invention, According to the objective, it can select suitably from well-known things, For example, waxes etc. are mentioned suitably. The melting point of the wax as the release agent is preferably 70 to 150 ° C. When the temperature is lower than 70 ° C., the heat-resistant storage stability of the toner is inferior. The amount of these release agents used is preferably 2 to 15% by weight based on the toner. If it is less than 2% by weight, the effect of preventing offset is insufficient, and if it exceeds 15% by weight, transferability and durability are deteriorated.

  A conventionally well-known thing can be used for the said wax. For example, low molecular weight polyethylene, low molecular weight polypropylene and other low molecular weight polyolefin waxes, synthetic hydrocarbon waxes such as Fischer-Tropsch wax, beeswax, carnauba wax, candelilla wax, rice wax, montan wax and other natural waxes, Examples include petroleum waxes such as paraffin wax and microcrystalline wax, higher fatty acids such as stearic acid, palmitic acid, and myristic acid, metal salts of higher fatty acids, higher fatty acid amides, synthetic ester waxes, and various modified waxes thereof. These waxes can be used alone or in combination of two or more.

  Of these, carnauba wax and its modified wax, polyethylene wax, and synthetic ester wax are preferably used. In particular, the synthetic ester wax pentaerythritol tetrabehenate is most preferred. The reason for this is that carnauba wax and its modified wax and synthetic ester wax are appropriately finely dispersed with respect to the polyester resin and polyol resin, so that the toner has excellent offset prevention, transferability and durability as described later. This is because it is easy.

(Charge control agent)
As the charge control agent used in the present invention, all known ones conventionally used can be used. For example, nigrosine dyes, triphenylmethane dyes, chromium-containing metal complex dyes, molybdate chelate pigments, rhodamine dyes, alkoxy amines, quaternary ammonium salts (including fluorine-modified quaternary ammonium salts), alkylamides, phosphorus Simple substance or compound, tungsten simple substance or compound, fluorine-based activator, salicylic acid metal salt, metal salt of salicylic acid derivative, and the like.

  Specifically, Bontron 03 of a nigrosine dye, Bontron P-51 of a quaternary ammonium salt, Bontron S-34 of a metal-containing azo dye, E-82 of an oxynaphthoic acid metal complex, E-84 of a salicylic acid metal complex , Phenolic condensate E-89 (above, Orient Chemical Industries, Ltd.), quaternary ammonium salt molybdenum complex TP-302, TP-415 (above, Hodogaya Chemical Co., Ltd.), quaternary ammonium salt copy Charge PSY VP2038, triphenylmethane derivative copy blue PR, quaternary ammonium salt copy charge NEG VP2036, copy charge NX VP434 (above, manufactured by Hoechst), LRA-901, boron complex LR-147 (above, Japan) Carlit), copper phthalocyanine, perylene, quinacridone Azo pigments, and other high molecular compounds having functional groups such as sulfonic acid groups, carboxyl groups, and quaternary ammonium salts.

  The content of the charge control agent is appropriately determined according to desired charging characteristics, but is preferably 0.1 to 10% by weight, more preferably 0.2 to 5% by weight with respect to the binder resin 100. preferable. When the addition amount exceeds 10% by weight, the chargeability of the toner is too high, the effect of the charge control agent is reduced, the electrostatic attraction with the developing roller is increased, the flowability of the developer is reduced, the image The concentration may decrease. On the other hand, if the addition amount is less than 0.1% by weight, the charge rising property and the charge amount are not sufficient, and the toner image may be easily affected.

(External additive)
In the toner of the present invention, inorganic fine particles (external additives) may be further added and mixed with the toner base particles produced as described above in order to improve the fluidity, storage stability, developability and transferability. For mixing such additives, a general powder mixer is used, but it is preferable to equip a jacket or the like to adjust the internal temperature. In order to change the load history applied to the additive, the additive may be added midway or gradually. In this case, you may change the rotation speed, rolling speed, time, temperature, etc. of a mixer. Alternatively, a strong load may be applied first, then a relatively weak load, or vice versa. Examples of the mixing equipment that can be used include a V-type mixer, a rocking mixer, a Ladige mixer, a Nauter mixer, and a Henschel mixer. Next, the toner is obtained by passing through a sieve of 250 mesh or more to remove coarse particles and aggregated particles.

  Specific examples of the inorganic fine particles (external additives) include, for example, silica, alumina, titanium oxide, barium titanate, magnesium titanate, calcium titanate, strontium titanate, zinc oxide, tin oxide, silica sand, clay, mica And wollastonite, diatomaceous earth, chromium oxide, cerium oxide, bengara, antimony trioxide, magnesium oxide, zirconium oxide, barium sulfate, barium carbonate, calcium carbonate, silicon carbide, silicon nitride, and the like.

  Such inorganic fine particles (external additives) can be surface-treated to increase hydrophobicity and prevent deterioration of flow characteristics and charging characteristics even under high humidity. For example, silane coupling agents, silylating agents, silane coupling agents having an alkyl fluoride group, organic titanate coupling agents, aluminum coupling agents, silicone oils, modified silicone oils and the like are preferable surface treatment agents. .

The primary particle diameter of the inorganic fine particles (external additive) is preferably 5 × ¹⁰ -3 ~2μm, it is particularly preferably 5 × ¹⁰ -3 ~0.5μm. Moreover, it is preferable that the specific surface area by BET method is 20-500 m < ² > / g. The amount of inorganic fine particles added is preferably 0.01 to 5% by weight of the toner.

(Weight average particle diameter of toner)
The weight average particle diameter of the toner is not particularly limited and can be appropriately selected according to the purpose. However, in order to obtain a high-quality image with excellent granularity, sharpness, and fine line reproducibility, the weight average particle diameter Is preferably 3.5 μm to 10 μm. The smaller the particle size, the better the image sharpness and fine line reproducibility. In particular, in a color image forming apparatus, the demand for image quality is strict and toner of 10 μm or less is required. In particular, 7.5 μm or less is preferable for image quality. On the other hand, if the toner particle size becomes too small, the fluidity and transferability of the toner deteriorate. Here, the weight average particle diameter of the toner can be obtained as follows.

[Measurement of weight average particle diameter (Dw) of toner]
As an apparatus for measuring the particle size distribution of toner particles by the Coulter counter method, there are Coulter Counter TA-II and Coulter Multisizer III (both manufactured by Coulter). In the present invention, measurement was performed as follows using Coulter Multisizer III.

  First, 0.1 to 5 ml of a surfactant, preferably polyoxyethylene alkyl ether, is added as a dispersant to 100 to 150 ml of an electrolytic aqueous solution. Here, the electrolytic solution is prepared by preparing an about 1% NaCl aqueous solution using primary sodium chloride, and for example, ISOTON-II (manufactured by Coulter) can be used. Here, 2 to 20 mg of a measurement sample is further added. The electrolytic solution in which the sample is suspended is subjected to a dispersion treatment with an ultrasonic disperser for about 1 to 3 minutes, and the measurement device is used to measure the volume and number of toner particles or toner using a 100 μm aperture as an aperture. Volume distribution and number distribution are calculated. From the obtained distribution, the weight average particle diameter (Dw) and the number average particle diameter (Dn) of the toner can be obtained.

  The channel in the above measurement is as follows: 2.00 to less than 2.52 μm; 2.52 to less than 3.17 μm; 3.17 to less than 4.00 μm; 4.00 to less than 5.04 μm; 5.04 to 6.35 μm Less than 6.35 to less than 8.00 μm; less than 8.00 to less than 10.08 μm; less than 10.08 to less than 12.70 μm; less than 12.70 to less than 16.00 μm; less than 16.00 to less than 20.20 μm; ≦ 25.40 μm; 25.40 to less than 32.00 μm; 13 channels of 32.00 to less than 40.30 μm are used, and particles having a particle diameter of 2.00 μm to less than 40.30 μm are targeted.

(Glass transition temperature (Tg) of toner)
The Tg of the image forming toner of the present invention is preferably 60 to 65 ° C. When Tg is higher than the above range, the lower limit fixing temperature of the toner is increased, so that the low temperature fixing property of the toner is deteriorated.
The Tg (DSC maximum endothermic peak) of the toner for image formation is tangent to the endothermic curve near the melting point using a TG-DSC system (TAS-100) manufactured by Rigaku Corporation and using an analysis system in the TAS-100 system. And calculated from the point of contact with the baseline.
That is, about 10 mg of a toner sample is placed in an aluminum sample container, which is placed on a holder unit and set in an electric furnace. Heating was performed from room temperature to 180 ° C. at a heating rate of 10 ° C./min, and calculation was performed based on the obtained endothermic curve.

(Developer)
The image forming toner of the present invention can be used as a one-component developer or a two-component developer. That is, the one-component developer is composed of only the image forming toner, and the two-component developer is composed of the image forming toner and the carrier.

[One-component developer]
In the one-component developer, it can be used as a non-magnetic one-component toner or a magnetic one-component toner (magnetic toner).
When used as a magnetic toner, a known magnetic material can be used. That is, magnetic materials contained in the magnetic toner include iron oxides such as magnetite, hematite, and ferrite, metals such as iron, cobalt, and nickel, or aluminum, cobalt, copper, lead, magnesium, tin, and the like of these metals. Examples include alloys of metals such as zinc, antimony, beryllium, bismuth, cadmium, calcium, manganese, selenium, titanium, tungsten, vanadium, and mixtures thereof. These ferromagnetic materials desirably have an average particle size of about 0.1 to 2 μm. The amount of the ferromagnetic material contained in the toner is 20 to 200 parts by weight, particularly preferably 100 parts by weight of the resin component, with respect to 100 parts by weight of the binder resin. 40 to 150 parts by weight per part.

[Two-component developer]
As the carrier used in the two-component developer of the present invention, conventionally known ones for two-component developers can be used.
For example, a carrier made of magnetic particles such as iron or ferrite, a resin-coated carrier in which such magnetic particles are coated with a resin, or a binder-type carrier in which magnetic fine powder is dispersed in a binder resin. Can be used.
Magnetic materials include iron oxides such as magnetite, hematite, and ferrite, metals such as iron, cobalt, and nickel, or aluminum, cobalt, copper, lead, magnesium, tin, zinc, antimony, beryllium, bismuth, cadmium, Metal alloys such as calcium, manganese, selenium, titanium, tungsten, vanadium and mixtures thereof can be used.

  Among these carriers, a silicone resin, a copolymer resin (graft resin) of an organopolysiloxane and a vinyl monomer, or a resin-coated carrier using a polyester resin can be used as a coating resin, such as toner spent. A carrier coated with a resin obtained by reacting an isocyanate with a copolymer resin of an organopolysiloxane and a vinyl monomer is preferable from the viewpoint of durability, environmental stability, and spent resistance. . As the vinyl monomer, it is necessary to use a monomer having a substituent such as a hydroxyl group reactive with isocyanate.

  In addition to the above, examples of carrier coating materials used for carriers include amino resins such as urea-formaldehyde resins, melamine resins, benzoguanamine resins, urea resins, polyamide resins, and epoxy resins. Polyvinyl resins and polyvinylidene resins, acrylic resins, polymethyl methacrylate resins, polyacrylonitrile resins, polyvinyl acetate resins, polyvinyl alcohol resins, polyvinyl butyral resins, polystyrene resins and styrene-acrylic copolymer resins, Halogenated olefin resins such as vinyl chloride, polyester resins such as polyethylene terephthalate resin and polybutylene terephthalate resin, polycarbonate resins, polyethylene resins, polyvinyl fluoride resins, polyvinylidene fluoride resins, polytrifluoroethylene resins, polyhexafluoropropylene Resin, copolymer of vinylidene fluoride and acrylic monomer, copolymer of vinylidene fluoride and vinyl fluoride, tetrafluoroethylene and fluoride Vinylidene fluoro such as terpolymers of non-fluorinated monomer, and silicone resins.

  Moreover, you may make conductive powder etc. contain as a filler in coating resin as needed. As the conductive powder, metal powder, carbon black, titanium oxide, tin oxide, zinc oxide, aluminum oxide, silica and the like can be used. These preferably have an average particle diameter of 1 μm or less. When the average particle diameter is larger than 1 μm, it is difficult to control electric resistance in the case of conductive powder.

  It is preferable to use a magnetic carrier having a volume average particle diameter of 20 to 100 μm, preferably 20 to 60 μm from the viewpoint of ensuring high image quality and preventing carrier fogging.

(Manufacture of toner)
The image forming toner of the present invention is obtained by pulverizing and classifying a compound containing at least a colorant and a binder resin after undergoing a melting and kneading process. An example of the manufacturing process will be described below. The image forming toner of the present invention is not limited to this.

As a method for producing the toner according to the present invention, first, a binder resin, a pigment or a dye as a colorant, and a compound containing a release agent, a charge control agent, and other additives as necessary. Is thoroughly mixed with a mixer such as a Henschel mixer. The blended mixture is converted into a continuous twin screw extruder (for example, KTK type twin screw extruder manufactured by Kobe Steel, TEM type twin screw extruder manufactured by Toshiba Machine Co., Ltd., PCM type twin screw extruder manufactured by Ikekai Tekko Co., Ltd.) KEX type twin screw extruder manufactured by Kurimoto Iron Works Co., Ltd., continuous single screw kneader (for example, Kousida manufactured by Buss Co., Ltd., KCK kneader), direct open roll type continuous kneader Needex (open roll) A thermal kneading machine such as a continuous kneading granulator, manufactured by Mitsui Mining Co., Ltd. can be used. At this time, as a method for increasing the specific energy, a method of decreasing the kneading amount or a method of lowering the kneader setting temperature and kneading the kneaded material in a high viscosity state is used.
Next, after cooling the kneaded product, it is coarsely pulverized using a hammer mill or the like, and further pulverized by a fine pulverizer or mechanical pulverizer using a jet stream, and a classifier using a swirling air stream or the Coanda effect is used. The image forming toner of the present invention is obtained by classifying to a predetermined particle size with a classifier.
Furthermore, inorganic fine particles as external additives and the above-classified toner are sufficiently mixed by a mixer such as a Henschel mixer and passed through a sieve of 250 mesh or more to remove coarse particles and aggregated particles, thereby forming an image. It may be used as a toner.

(Image forming method)
The image forming method of the present invention comprises at least a charging step for charging the surface of an image carrier, an electrostatic latent image forming step for forming an electrostatic latent image on the image carrier, and the electrostatic latent image for image formation. A development process for forming a visible image by developing with toner, a transfer process for transferring the visible image onto a recording medium to form an unfixed image, and fixing the unfixed image on the recording medium The image forming method includes a fixing step, and the image forming toner used for forming the visible image is the image forming toner described above. Here, the toner for image formation can be satisfactorily fixed even if the conveyance speed of the recording medium in the fixing step is 280 mm / second or more.

  Next, the image forming method of the present invention will be described with reference to FIG. The image forming apparatus shown in FIG. 1 includes a photosensitive member 10, a charging device 20, an exposure device 30, a developing device 40, an intermediate transfer member 50, a cleaning device 60 having a cleaning blade, a charge eliminating device 70, a transfer device. A device 80 is provided. Note that a charging roller is used as the charging device 20, a static elimination lamp as the static elimination device 70, and a transfer roller as the transfer device 80.

The intermediate transfer member 50 is an endless belt, and is designed to be stretched by three support rollers 51 arranged on the inner side thereof so as to be movable in the arrow direction. A part of the three support rollers 51 also functions as a transfer bias roller capable of applying a predetermined transfer bias (primary transfer bias) to the intermediate transfer member 50. The intermediate transfer member 50 is provided with a cleaning device 90 having a cleaning blade in the vicinity thereof. Further, a transfer device 80 capable of applying a secondary transfer bias for transferring a visible image (secondary transfer) to the transfer target 95 is disposed opposite to the transfer device 80. Around the intermediate transfer member 50, a corona charger 58 for applying a charge to the visible image on the intermediate transfer member 50 is in contact with the photosensitive member 10 and the intermediate transfer member 50 in the rotation direction of the intermediate transfer member 50. And the contact portion between the intermediate transfer body 50 and the transfer body 95.
Note that transfer paper is used as the transfer target 95.

  The developing device 40 includes a developing belt 41 as a developer carrier, and a black developing unit 45K, a yellow developing unit 45Y, a magenta developing unit 45M, and a cyan developing unit 45C provided around the developing belt 41. ing. The developing unit 45K includes a developer accommodating portion 42K, a developer supplying roller 43K, and a developing roller 44K, and the developing unit 45Y includes a developer accommodating portion 42Y, a developer supplying roller 43Y, and a developing roller 44Y. The developing unit 45M includes a developer accommodating portion 42M, a developer supply roller 43M, and a developing roller 44M. The developing unit 45C includes a developer accommodating portion 42C, the developer supplying roller 43C, and the developing roller 44C. Yes. The developing belt 41 is an endless belt, is rotatably stretched around a plurality of belt rollers, and a part thereof is in contact with the photoconductor 10.

In this image forming apparatus, after the charging device 20 uniformly charges the photoconductor 10, the exposure device 30 performs imagewise exposure on the photoconductor 10 to form an electrostatic latent image. Next, the developing device 40 supplies the developer to the electrostatic latent image formed on the photoconductor 10 and develops it to form a visible image.
The visible image is transferred (primary transfer) onto the intermediate transfer body 50 by the voltage applied from the support roller 51 and further transferred (secondary transfer) onto the transfer body 95. As a result, a transfer image is formed on the transfer target 95. The toner remaining on the photoconductor 10 is removed by the cleaning device 60, and the charge of the photoconductor 10 is removed by the charge eliminating lamp 70.

Next, another aspect of the image forming method of the present invention will be described with reference to FIG. The image forming apparatus shown in FIG. 2 has a black developing unit 45K, a yellow developing unit 45Y, a magenta developing unit 45M, and a cyan around the photosensitive member 10, instead of the developing device 40 in the image forming apparatus shown in FIG. The developing unit 45C has the same configuration as that of the image forming apparatus shown in FIG.
In FIG. 2, the same components as those in the image forming apparatus shown in FIG. The same applies to FIGS. 3 and 4 described later.

  Next, another aspect of the image forming method of the present invention will be described with reference to FIG. The image forming apparatus shown in FIG. 3 is a tandem type color image forming apparatus. The image forming apparatus includes a copying apparatus main body 150, a paper feed table 200, a scanner 300, and an automatic document feeder (ADF) 400.

  The copying apparatus main body 150 is provided with an endless belt-like intermediate transfer member 50 at the center. The intermediate transfer member 50 is stretched around the support rollers 14, 15, and 16 and can rotate clockwise in FIG. 3. A cleaning device 17 for removing residual toner on the intermediate transfer member 50 is disposed in the vicinity of the support roller 15. On the intermediate transfer member 50 stretched by the support roller 14 and the support roller 15, four image forming units 18 of yellow, cyan, magenta, and black are arranged opposite to each other along the conveying direction. A means 120 is arranged. An exposure device 21 is disposed in the vicinity of the image forming unit 120. The secondary transfer device 22 is disposed on the side of the intermediate transfer member 50 opposite to the side on which the image forming unit 120 is disposed. In the secondary transfer device 22, a secondary transfer belt 24, which is an endless belt, is stretched around a pair of support rollers 23, and the recording paper conveyed on the secondary transfer belt 24 and the intermediate transfer member 50 are mutually connected. It is possible to touch. A fixing device 25 is disposed in the vicinity of the secondary transfer device 22. The fixing device 25 includes a fixing belt 26 that is an endless belt and a pressure roller 27 that is pressed against the fixing belt 26. A reversing device 28 for reversing the recording paper is disposed in the vicinity of the secondary transfer device 22 and the fixing device 25 in order to form images on both sides of the recording paper.

  Next, formation of a full-color image (color copy) using the image forming unit 120 will be described. First, an original document is set on the document table 130 of the automatic document feeder (ADF) 400 or the automatic document feeder 400 is opened, and the original document is set on the contact glass 32 of the scanner 300. Close.

  When a start switch (not shown) is pressed, when the document is set on the automatic document feeder 400, the document is transported and moved onto the contact glass 32, and then the document is set on the contact glass 32. When this happens, the scanner 300 is immediately driven, and the first traveling body 33 and the second traveling body 34 travel. At this time, light from the light source is irradiated by the first traveling body 33, and reflected light from the document surface is reflected by a mirror in the second traveling body 34. Further, the image is received by the reading sensor 36 through the imaging lens 35, and the original is read to obtain image information of black, yellow, magenta and cyan. Next, each image information is transmitted to each image forming unit 18 in the image forming means 120, and a visible image of each color of black, yellow, magenta and cyan is formed.

  As shown in FIG. 4, the image forming unit 18 includes a photoconductor 10, a charging device (not indicated) for uniformly charging the photoconductor 10, and an exposure device 21, based on each image information. The electrostatic latent image formed by exposing the photosensitive member 10 to the toner is developed using each toner (black toner, yellow toner, magenta toner, and cyan toner) to form a visible image with each toner. It includes a device (no code), a transfer charger (no code) for transferring a visible image onto the intermediate transfer member 50, a cleaning device (no code), and a charge eliminating device (no code). Based on this, it is possible to form a visible image of each color. Next, the visible images of the respective colors are sequentially transferred (primary transfer) onto the intermediate transfer body 50 that is rotated and moved by the support rollers 14, 15 and 16, and the visible images of the respective colors are superimposed to form a composite transfer image. It is formed.

  On the other hand, in the paper feed table 200, one of the paper feed rollers 142 is selectively rotated to feed the recording paper from one of the paper feed cassettes 144 provided in multiple stages in the paper bank 143, and one sheet at a time by the separation roller 145. The paper is separated and sent to the paper feed path 146, transported by the transport roller 147, guided to the paper feed path 148 in the copying machine main body 150, and abutted against the registration roller 49 to stop. Alternatively, the paper feed roller 142 is rotated to feed out the recording paper on the manual feed tray 54, separated one by one by the separation roller 52, put into the manual paper feed path 53, and abutted against the registration roller 49 and stopped. The registration roller 49 is generally used while being grounded, but may be used in a state where a bias is applied to remove paper dust from the recording paper. Then, the registration roller 49 is rotated in synchronization with the composite transfer image formed on the intermediate transfer member 50, and the recording paper is sent between the intermediate transfer member 50 and the secondary transfer device 22, so that the secondary transfer device. By transferring the composite transfer image onto the recording paper (secondary transfer) by 22, a color image is formed on the recording paper. The toner remaining on the intermediate transfer member 50 is removed by the cleaning device 17.

  The recording paper on which the color image is formed is conveyed by the secondary transfer device 22 and sent to the fixing device 25, where the composite transfer image is heated and pressed and fixed on the recording paper. Thereafter, the recording paper is switched by the switching claw 55 and discharged by the discharge roller 56 and is stacked on the discharge tray 57. Alternatively, it is switched by the switching claw 55 and reversed by the reversing device 28 and led to the transfer position again. After an image is formed also on the back surface, the sheet is discharged by the discharge roller 56 and stacked on the discharge tray 57.

  According to the image forming method of the present invention, an image forming toner that has excellent low-temperature fixability and heat-resistant storage stability even at high speed and is fixed only at a desired position on a recording medium without causing an offset phenomenon is used. Therefore, even when an image is formed by an electrophotographic image forming apparatus having a high output speed, it is excellent in glossiness, and it is possible to stably output a high-quality image without generating a ghost or the like.

(Image forming device)
In addition, as described above, the image forming apparatus of the present invention includes at least an image carrier, charging means for charging the surface of the image carrier, and exposure of the charged image carrier surface to form an electrostatic latent image. An exposure unit for forming, a developing unit for developing the electrostatic latent image using an image forming toner to form a visible image, and transferring the developed toner image onto a recording medium to form an unfixed image. An image forming apparatus comprising a transfer unit for forming and a fixing unit for fixing the unfixed image to the recording medium, wherein the image forming toner used for forming the visible image is the above-described toner. It is an image forming toner.

  According to the image forming apparatus of the present invention, an image forming toner that has excellent low-temperature fixability and heat-resistant storage stability even at high speed and is fixed only at a desired position on a recording medium without causing an offset phenomenon is used. Therefore, even if the process line speed is high, an abnormal image is not generated and the image can be fixed stably. For example, if a tandem full-color image forming apparatus is used, a higher-quality image can be output at a higher speed. Further, if the image forming method and the image forming apparatus of the present invention are used, it can be widely applied to electrophotographic application fields using electrophotography (for example, electrostatic copying machines and laser beam printers).

Further, the image forming means as described above may be fixedly incorporated in the copying apparatus, facsimile, or printer, but may be incorporated in these apparatuses in the form of a process cartridge.
The process cartridge is an apparatus (part) that contains an image carrier (photoconductor) and further includes a means selected from a charging unit, an exposure unit, a developing unit, a transfer unit, and a cleaning unit. If necessary, other means such as a static elimination means may be included. There are many shapes and the like of the process cartridge, but a general example is the one shown in FIG.
Here, the process cartridge includes a photosensitive member (101), and includes a charging unit (102), an exposure unit (103), a developing unit (104), and a cleaning unit (107). It has the means of. In the figure, reference numeral 105 denotes a recording medium (transfer body), and 106 denotes transfer means.

  That is, the process cartridge of the present invention includes an image carrier, a charging unit that charges the surface of the image carrier, an exposure unit that exposes the charged image carrier surface to form an electrostatic latent image, and a formed static charge. It is selected from developing means for developing the electrostatic latent image using image forming toner, transfer means for transferring the developed toner image to the recording medium, and cleaning means for removing the toner remaining on the surface of the image carrier after the transfer. A process cartridge which can be attached to and detached from an image forming apparatus main body integrated with at least one means, and the image forming toner used is the image forming toner of the present invention. It is. It should be noted that other means (for example, static elimination means) may be included as necessary as at least one means to be selected.

  In the process cartridge of the present invention, since the image forming toner of the present invention is supplied from the developing unit, the fixing unit is stably fixed only at a desired position on the recording medium without causing an offset phenomenon due to an unfixed image. High quality images can be output. In addition, it is easy to store and transport and has excellent handling properties.

  EXAMPLES Hereinafter, although an Example and a comparative example are given and this invention is demonstrated further more concretely, this invention is not restrict | limited by these Examples. In the following description, “parts” means parts by weight unless otherwise specified.

  Polyester resin 1 used for the following toner formulation was synthesized as follows.

(Synthesis of polyester resin 1)
440 parts of PO adduct of bisphenol A (propylene oxide added to bisphenol A: hydroxyl value 320 mgKOH / g) in a reaction vessel equipped with a thermometer, stirrer, cooler and nitrogen introduction tube, 135 parts of diethylene glycol, terephthalic acid 211 parts, 211 parts of fumaric acid and 2.5 parts of dibutyltin oxide were added and reacted at 180 ° C. until the acid value reached 7, to obtain [Polyester Resin 1]. [Polyester resin 1] had a Tg of 65 ° C. and a weight average molecular weight of 16000. The weight average molecular weight of the polyester resin 1 was measured using GPC manufactured by Waters, and Tg was measured using a TG-DSC system (TAS-100) manufactured by Rigaku Corporation (hereinafter the same).

(Synthesis of polyester resin 2)
[Polyester resin 2] was synthesized under the same conditions except that the polyester resin 1 was reacted at 160 ° C. until the acid value reached 10 mgKOH / g. [Polyester resin 2] had a Tg of 62 ° C. and a weight average molecular weight of 10,000.

(Synthesis of polyester resin 3)
[Polyester Resin 3] was synthesized under the same conditions except that the polyester resin 1 was reacted at 200 ° C. until the acid value reached 7 mgKOH / g. [Polyester resin 3] had a Tg of 65 ° C. and a weight average molecular weight of 26,000.

(Synthesis of polyester resin 4)
[Polyester resin 4] was synthesized under the same conditions except that the amount of terephthalic acid was 371 parts and the amount of fumaric acid was 51 parts. [Polyester resin 4] had a Tg of 63 ° C. and a weight average molecular weight of 16000.

(Synthesis of polyester resin 5)
[Polyester resin 5] was synthesized under the same conditions except that the amount of terephthalic acid was 261 parts and the amount of fumaric acid was 161 parts. [Polyester resin 5] had a Tg of 64 ° C. and a weight average molecular weight of 16000.

(Synthesis of polyester resin 6)
[Polyester resin 6] was synthesized under the same conditions except that the amount of terephthalic acid was 51 parts and the amount of fumaric acid was 371 parts. [Polyester resin 6] had a Tg of 62 ° C. and a weight average molecular weight of 16000.

(Synthesis of polyester resin 7)
[Polyester resin 7] was synthesized by the same method as the synthesis of polyester resin 1 except that fumaric acid which is an acid component used in the synthesis of polyester resin 1 was not used and terephthalic acid was used instead. This [polyester resin 7] does not have a double bond.

(Synthesis of polyester resin 8)
[Polyester Resin 8] was synthesized under the same conditions except that the polyester resin 1 was reacted at 230 ° C. until the acid value reached 7 mgKOH / g. [Polyester resin 8] had a Tg of 75 ° C. and a weight average molecular weight of 48,000.

(Synthesis of polyester resin 9)
[Polyester resin 9] was synthesized under the same conditions except that the amount of terephthalic acid was 381 parts and the amount of fumaric acid was 41 parts. [Polyester resin 9] had a Tg of 63 ° C. and a weight average molecular weight of 16000.

(Adjustment of master batch 1)
A master batch 1 (prepared by uniformly dispersing a colorant in a part of the polyester resin 1) used for toner formulation was prepared as follows.
The materials shown in the following masterbatch 1 formulation were mixed for 3 minutes at 1500 rpm using a Henschel mixer (Henschel 20B: Mitsui Mining Co., Ltd.), and the resulting mixture was 45 minutes at 120 ° C. using two rolls. After kneading, rolling and cooling and pulverization with a pulverizer gave a master batch 1.
[Prescription of Masterbatch 1]
Water: 25 parts Copper phthalocyanine (Toyo Ink Co., Ltd.): 50 parts Polyester resin 1: 50 parts

(Preparation of crosslinking agent 1)
75 parts of diglyceryl monostearate (manufactured by Sakamoto Yakuhin Kogyo Co., Ltd.) as a pigment dispersant and 25 parts of benzoyl peroxide (manufactured by Merck Co., Ltd.) as a crosslinking initiator at 1000 rpm using a Henschel mixer (Henschel 20B: Mitsui Mining Co., Ltd.) For 3 minutes and kneading in a single-screw kneader (small bus co-kneader: manufactured by Buss) under the conditions of set temperature: inlet portion 60 ° C., outlet portion 40 ° C., feed amount: 10 kg / hr [ Crosslinking agent 1] was obtained.

(Preparation of crosslinking agent 2)
[Crosslinking agent 2] was obtained under the same conditions except that 99.9 parts of diglyceryl monostearate and 0.1 part of benzoyl peroxide were used.

(Preparation of crosslinking agent 3)
[Crosslinking agent 3] was obtained under the same conditions except that 50 parts of diglyceryl monostearate and 50 parts of benzoyl peroxide were used as preparation conditions for the crosslinking agent 1.

(Preparation of crosslinking agent 4)
Henschel mixer (Henschel 20B: Mitsui Mining Co., Ltd.) 75 parts of hexaglyceryl octastearate (manufactured by Sakamoto Yakuhin Kogyo Co., Ltd., molecular weight: 2582) as a pigment dispersant and 25 parts of benzoyl peroxide (manufactured by Merck) as a crosslinking initiator The mixture is mixed at 1000 rpm for 3 minutes using a single-screw kneader (small bus co-kneader: manufactured by Buss) under the conditions of set temperature: inlet 60 ° C., outlet 40 ° C., feed amount: 10 kg / hr. Kneading was performed to obtain [Crosslinking agent 4].

(Preparation of crosslinking agent 5)
[Crosslinking agent 5] was obtained under the same conditions except that 45 parts of diglyceryl monostearate and 55 parts of benzoyl peroxide were used.

(Preparation of crosslinking agent 6)
75 parts of glycerin (molecular weight: 108) as a pigment dispersant and 25 parts of benzoyl peroxide (manufactured by Merck) as a crosslinking initiator are mixed at 1000 rpm for 3 minutes using a Henschel mixer (Henschel 20B: manufactured by Mitsui Mining). [Crosslinking agent 6] is obtained by kneading in a uniaxial kneader (small bus co-kneader: Buss) under the conditions of set temperature: inlet portion 60 ° C., outlet portion 40 ° C., feed amount: 10 kg / hr. It was.

(Preparation of cross-linking agent 7)
75 parts of paraffin (molecular weight: 3500) as a pigment dispersant and 25 parts of benzoyl peroxide (manufactured by Merck) as a crosslinking initiator are mixed at 1000 rpm for 3 minutes using a Henschel mixer (Henschel 20B: manufactured by Mitsui Mining). [Crosslinking agent 6] is obtained by kneading in a uniaxial kneader (small bus co-kneader: Buss) under the conditions of set temperature: inlet portion 60 ° C., outlet portion 40 ° C., feed amount: 10 kg / hr. It was.

[Example 1]
(Manufacture of image forming toner 1)
Using the polyester resin 1, the master batch 1, the crosslinking agent 1 and the paraffin wax (HNP-11, manufactured by Nippon Seiki Co., Ltd.) obtained above, an image forming toner 1 was produced according to the following formulation.
Polyester resin 1: 96 parts Paraffin wax: 5 parts Masterbatch 1: 8 parts Crosslinker 1: 2 parts

  The materials shown in the prescription of the image forming toner 1 were mixed at 1500 rpm for 3 minutes using a Henschel mixer (Henschel 20B: manufactured by Mitsui Mining Co., Ltd.), and a uniaxial kneader (small bus co-kneader: manufactured by Buss). Then, kneading was carried out under the conditions of set temperature: inlet portion 90 ° C., outlet portion 60 ° C., feed amount: 10 kg / Hr to obtain [base toner 1].

Further, the above [base toner 1] is kneaded and then cooled by rolling, pulverized by a pulverizer, and further, air pressure by using a flat impact plate in an I-type mill (manufactured by Nippon Pneumatic Co., Ltd .: IDS-2 type). Fine pulverization was performed under the conditions of 6.0 atm / cm ² and feed amount: 0.5 kg / hr, followed by classification (132MP manufactured by Alpine) to obtain [Toner Base Particles 1].

Thereafter, 100 parts of [toner base particle 1], 1.0 part of hydrophobic silica (external additive A) having a primary particle diameter of 10 nm as an external additive, a primary particle diameter of 110 nm produced by a sol-gel method, and substantially spherical hexamethyl. 1.0 part of disilazane hydrophobized silica (external additive B) and 1.0 part of hydrophobic titanium oxide (external additive C) having a primary particle size of 15 nm were added to a Henschel mixer (Henschel 20B manufactured by Mitsui Mining Co., Ltd.). And mixed to obtain a toner.
The above mixing conditions were mixed by repeating the set of rotating for 30 seconds and stopping rotation for 60 seconds 5 times at a peripheral speed of 30 m / sec. The toner obtained here is referred to as [Toner 1].

[Toner 1] had a weight average particle diameter (Dw) of 6.8 μm and a number average particle diameter (Dn) of 6.0 μm. The weight average particle diameter (Dw) and the number average particle diameter (Dn) were measured using the aforementioned Coulter Multisizer III. [Toner 1] had a weight average molecular weight of 24,000 and Tg of 62 ° C. The weight average molecular weight of the polyester resin 1 was measured using GPC manufactured by Waters, and Tg was measured using a TG-DSC system (TAS-100) manufactured by Rigaku Corporation (hereinafter the same).
FIG. 6 is a micrograph of [Toner 1]. The part that looks like a white line is the release agent, but there is no binder resin interface and the pigment is well dispersed in all parts of the toner. Indicates that it is not shown.

[Example 2]
(Manufacture of image forming toner 2)
[Toner 2] was produced in the same manner as in [Toner 1] produced in Example 1, except that [Polyester resin 2] was used instead of [Polyester resin 1]. [Toner 2] had a weight average particle diameter (Dw) of 6.7 μm and a number average particle diameter (Dn) of 6.1 μm.

Example 3
(Manufacture of image forming toner 3)
[Toner 3] was produced in the same manner as in [Toner 1] produced in Example 1, except that [Polyester resin 3] was used instead of [Polyester resin 1]. [Toner 3] had a weight average particle diameter (Dw) of 6.9 μm and a number average particle diameter (Dn) of 6.0 μm.

Example 4
(Manufacture of toner 4 for image formation)
[Toner 4] was produced in the same manner as in [Toner 1] produced in Example 1, except that the addition amount of [Crosslinking agent 1] was 1 part. [Toner 4] had a weight average particle diameter (Dw) of 7.1 μm and a number average particle diameter (Dn) of 6.2 μm.

Example 5
(Manufacture of image forming toner 5)
[Toner 5] was produced in the same manner as in [Toner 1] produced in Example 1, except that the amount of [Crosslinking agent 1] added was 5 parts. [Toner 5] had a weight average particle diameter (Dw) of 7.1 μm and a number average particle diameter (Dn) of 6.2 μm.

Example 6
(Manufacture of image forming toner 6)
[Toner 6] was produced in the same manner as in [Toner 1] produced in Example 1, except that [Polyester resin 4] was used instead of [Polyester resin 1]. [Toner 6] had a weight average particle diameter (Dw) of 6.8 μm and a number average particle diameter (Dn) of 6.1 μm.

Example 7
(Manufacture of image forming toner 7)
[Toner 7] was produced in the same manner as in [Toner 1] produced in Example 1, except that [Polyester resin 5] was used instead of [Polyester resin 1]. [Toner 7] had a weight average particle diameter (Dw) of 6.8 μm and a number average particle diameter (Dn) of 6.1 μm.

Example 8
(Manufacture of image forming toner 8)
[Toner 8] was produced in the same manner as in [Toner 1] produced in Example 1, except that [Polyester resin 6] was used instead of [Polyester resin 1]. [Toner 8] had a weight average particle diameter (Dw) of 6.7 μm and a number average particle diameter (Dn) of 6.1 μm.

Example 9
(Manufacture of image forming toner 9)
[Toner 9] was produced in the same manner as in [Toner 1] produced in Example 1, except that [Crosslinking agent 2] was used instead of [Crosslinking agent 1]. [Toner 9] had a weight average particle diameter (Dw) of 6.9 μm and a number average particle diameter (Dn) of 6.2 μm. [Toner 9] had a weight average molecular weight of 19000 and Tg of 62 ° C.

Example 10
(Manufacture of image forming toner 10)
[Toner 10] was produced in the same manner as in [Toner 1] produced in Example 1, except that [Crosslinking agent 3] was used instead of [Crosslinking agent 1]. [Toner 10] had a weight average particle diameter (Dw) of 6.8 μm and a number average particle diameter (Dn) of 6.0 μm. [Toner 10] had a weight average molecular weight of 23,000 and Tg of 62 ° C.

Example 11
(Manufacture of image forming toner 11)
[Toner 11] was produced in the same manner as in [Toner 1] produced in Example 1, except that [Crosslinking agent 4] was used instead of [Crosslinking agent 1]. [Toner 11] had a weight average particle diameter (Dw) of 6.8 μm and a number average particle diameter (Dn) of 6.0 μm. [Toner 11] had a weight average molecular weight of 25,000 and Tg of 62 ° C.

[Comparative Example 1]
(Manufacture of image forming toner 12)
[Toner 12] was produced in the same manner as in [Toner 1] produced in Example 1, except that [Polyester resin 7] was used instead of [Polyester resin 1]. [Toner 12] had a weight average particle diameter (Dw) of 6.9 μm and a number average particle diameter (Dn) of 6.1 μm. [Toner 12] had a weight average molecular weight of 14,000 and Tg of 62 ° C.

[Comparative Example 2]
(Manufacture of image forming toner 13)
In the prescription of [Toner 1] produced in Example 1, except that [Crosslinking agent 1] was not used, a toner was prepared by the same prescription and construction method as [Toner 13]. [Toner 13] had a weight average particle diameter (Dw) of 6.9 μm and a number average particle diameter (Dn) of 6.0 μm. [Toner 13] had a weight average molecular weight Mw of 15000 and Tg of 62 ° C.

[Comparative Example 3]
(Manufacture of image forming toner 14)
A toner was produced by the same method as [Toner 1], except that the toner formulation was as follows, and designated as [Toner 14].
Polyester resin 1: 71 parts Polyester resin 8: 25 parts Paraffin wax: 5 parts Master batch 1: 8 parts [Toner 14] has a weight average particle diameter (Dw) of 6.9 μm and a number average particle diameter (Dn) of 6. It was 1 μm. [Toner 14] had a weight average molecular weight Mw of 25,000 and Tg of 66 ° C.
FIG. 7 is a micrograph of [Toner 14], and the part that appears white is the release agent. There is an interface of the binder resin layer, and the black portion indicates that the pigment is not well dispersed in the toner.

[Comparative Example 4]
(Manufacture of image forming toner 15)
A toner was produced by the same method as [Toner 1], except that the toner formulation was as follows, and designated as [Toner 15].
Polyester resin 1: 21 parts Polyester resin 8: 75 parts Paraffin wax: 5 parts Masterbatch 1: 8 parts [Toner 15] has a weight average particle diameter (Dw) of 6.9 μm and a number average particle diameter (Dn) of 6. It was 1 μm. [Toner 15] had a weight average molecular weight Mw of 45,000 and Tg of 66 ° C.

[Comparative Example 5]
(Manufacture of image forming toner 16)
[Toner 16] was produced in the same manner as in [Toner 1] produced in Example 1, except that [Polyester resin 9] was used instead of Polyester resin 1]. [Toner 16] had a weight average particle diameter (Dw) of 6.8 μm and a number average particle diameter (Dn) of 6.1 μm. [Toner 16] had a weight average molecular weight of 18,000 and Tg of 62 ° C.

[Comparative Example 6]
(Manufacture of image forming toner 17)
In the formulation of [Toner 1] produced in Example 1, [Polyester resin 2] was used instead of [Polyester resin 1], and the amount of [Crosslinking agent 1] was changed to 1 part. [Toner 17] was produced. [Toner 17] had a weight average particle diameter (Dw) of 6.7 μm and a number average particle diameter (Dn) of 6.0 μm. [Toner 17] had a weight average molecular weight of 15,000 and Tg of 62 ° C.

[Comparative Example 7]
(Manufacture of image forming toner 18)
[Toner 18] was produced in the same manner as in [Toner 1] produced in Example 1, except that 2 parts of diglyceryl monostearate was used instead of [Crosslinking agent 1]. [Toner 18] had a weight average particle diameter (Dw) of 6.9 μm and a number average particle diameter (Dn) of 6.0 μm. [Toner 18] had a weight average molecular weight of 15,000 and Tg of 58 ° C.

[Comparative Example 8]
(Manufacture of image forming toner 19)
[Toner 19] was produced in the same manner as in [Toner 1] produced in Example 1, except that 2 parts of [Crosslinking agent 5] was used instead of [Crosslinking agent 1]. [Toner 19] had a weight average particle diameter (Dw) of 6.7 μm and a number average particle diameter (Dn) of 6.1 μm. [Toner 19] had a weight average molecular weight of 90,000 and Tg of 60 ° C.

[Comparative Example 9]
(Manufacture of image forming toner 20)
[Toner 20] was produced in the same manner as in [Toner 1] produced in Example 1, except that 2 parts of [Crosslinking agent 6] was used instead of [Crosslinking agent 1]. [Toner 20] had a weight average particle diameter (Dw) of 6.7 μm and a number average particle diameter (Dn) of 6.1 μm. [Toner 20] had a weight average molecular weight of 25,000 and Tg of 50 ° C.

[Comparative Example 10]
(Manufacture of image forming toner 21)
[Toner 21] was produced in the same manner as in [Toner 1] produced in Example 1, except that 2 parts of [Crosslinking agent 7] was used instead of [Crosslinking agent 1]. [Toner 21] had a weight average particle diameter (Dw) of 6.7 μm and a number average particle diameter (Dn) of 6.1 μm. [Toner 21] had a weight average molecular weight of 24,000 and Tg of 65 ° C.

  The following evaluations were performed on the toners 1 to 21 obtained as described above (Examples 1 to 11: Toners 1 to 11, Comparative Examples 1 to 10: Toners 12 to 21). The evaluation results are shown in Table 1.

[Evaluation of fixed image]
The following image evaluation test was performed using a Ricoh copier imageo Neo C600 and mixing [Toner 1] to [Toner 21] with a carrier used in the copier.
A toner sample having an adhesion amount of 0.4 mg / cm ² was prepared on an A4 size paper (T6000 70W T, manufactured by Ricoh), and a 3 cm × 5 cm rectangular image was formed at a position 3 cm from the front end of the paper surface. The fixing member was fixed at a linear velocity of 280 mm / sec after always controlling the temperature of the fixing member to 160 ° C. Next, the coloring power of this image was evaluated by X-Rite (manufactured by X-Rite Co., Ltd.) in status A mode. A case where the ID is less than 1.2 is regarded as rejected (x).

[Evaluation of fixing release temperature range]
Using [Toner 1] to [Toner 21] obtained above, evaluation of fixability (evaluation of cold offset and hot offset) was performed according to the following evaluation method.
<Cold offset>
Evaluation of low-temperature fixability was performed by visual confirmation of cold offset as follows.
The following image evaluation test was performed using a Ricoh copier imageo Neo C600 and mixing [Toner 1] to [Toner 21] with a carrier used in the copier.
A toner sample having an adhesion amount of 0.85 mg / cm ² is prepared on an A4 size paper (T6000 70W T-th, manufactured by Ricoh Co., Ltd.) with an image of a 3 cm × 5 cm rectangle at a position of 5 cm from the front end of the paper surface. The fixing member was constantly controlled at 140 ° C. and fixed at a linear speed of 300 mm / sec (toner weight was calculated from the weight of the paper before and after image output). At this time, the presence or absence of offset generation was evaluated by visual inspection of the tester. At this time, the toner was determined to be acceptable (◯) only when no offset was observed at 140 ° C. The other results are shown in Table 1 below.
In Table 1 below, the presence or absence of the occurrence of cold offset is indicated as follows.
・ No cold offset: ○
・ With cold offset: ×
<Hot offset>
Except that the temperature of the fixing member was always controlled at 180 ° C., the hot offset evaluation was performed under the same conditions as in the cold offset evaluation.
In Table 1 below, presence or absence of occurrence of hot offset is indicated as follows.
・ No hot offset: ○
・ With hot offset: ×

  The evaluation results are as shown in Table 1. In [Toner 1] to [Toner 11], all of the image ID and the fixing temperature range passed the evaluation conditions, but in [Toner 12] to [Toner 21], the evaluation results were evaluated. The condition was not met.

10 Photoconductor (Photoconductor drum)
10K black photoconductor 10Y yellow photoconductor 10M magenta photoconductor 10C cyan photoconductor 14 support roller 15 support roller 16 support roller 17 intermediate transfer cleaning device 18 image forming means 20 charging roller 21 exposure device 22 secondary transfer device 23 Roller 24 Secondary transfer belt 25 Fixing device 26 Fixing belt 27 Pressure roller 28 Sheet reversing device 30 Exposure device 32 Contact glass 33 First traveling member 34 Second traveling member 35 Imaging lens 36 Reading sensor 40 Developing device 41 Developing belt 42K Developer container 42Y Developer container 42M Developer container 42C Developer container 43K Developer supply roller 43Y Developer supply roller 43M Developer supply roller 43C Developer supply roller 44K Developer roller 44Y Developer roller 44M Developer Roller 44C Developing roller 45K Black developing unit 45Y Yellow developing unit 45M Magenta developing unit 45C Cyan developing unit 49 Registration roller 50 Intermediate transfer member 51 Roller 52 Separating roller 53 Manual feed path 54 Manual feed tray 55 Switching claw 56 Discharge roller 57 discharge tray 58 corona charger 60 cleaning device 61 developing device 62 transfer charger 63 photoconductor cleaning device 64 discharger 70 discharger lamp 80 transfer roller 90 cleaning device 95 transfer paper 100 image forming device 101 photoconductor 102 charging means 103 exposure 104 Developing means 105 Recording medium 107 Cleaning means 108 Transfer means 120 Tandem developer 130 Document table 142 Paper feed roller 143 Paper bank 144 Paper feed cassette 145 Separating roller 14 Feeding path 147 transport rollers 148 feed path 150 copier main body 200 feeder table 300 Scanner 400 automatic document feeder (ADF)

JP 2007-72333 A JP 2007-206097 A Japanese Patent No. 3478963 Japanese Patent No. 3044595

Claims (13)

A pulverized toner containing at least a colorant and a binder resin,
The binder resin has an unsaturated bond, and the unsaturated bond forms a crosslinking point by adding a pigment dispersant in which a crosslinking initiator is dissolved or dispersed and then melt-kneading.
An image forming toner characterized by the above.   The image forming toner according to claim 1, wherein the binder resin contains a polyester resin as a main component.   The image forming toner according to claim 2, wherein the amount of the pigment dispersant added is 1 to 5 parts by weight with respect to 100 parts by weight of the binder resin.   The toner for electrophotography according to any one of claims 1 to 3, wherein the pigment dispersant has a weight average molecular weight of 400 to 3,000.   The image forming toner according to claim 1, wherein the toner has a weight average molecular weight of 18000 or more.   The image forming toner according to claim 1, wherein the toner has a weight average particle diameter of 3.5 μm to 10 μm.   A one-component developer comprising the image forming toner according to claim 1.   A two-component developer comprising the image forming toner according to claim 1 and a carrier. A charging process for charging at least the surface of the image bearing member, an electrostatic latent image forming process for forming an electrostatic latent image on the image bearing member, and development of the electrostatic latent image using image forming toner. Image formation comprising: a development step for forming a visual image; a transfer step for transferring the visible image onto a recording medium to form an unfixed image; and a fixing step for fixing the unfixed image to the recording medium. A method,
The image forming method according to claim 1, wherein the image forming toner used for forming the visible image is the image forming toner according to claim 1.   The image forming method according to claim 9, wherein a conveyance speed of the recording medium in the fixing step is 280 mm / second or more. At least an image carrier, a charging unit that charges the surface of the image carrier, an exposure unit that exposes the charged image carrier surface to form an electrostatic latent image, and forms the electrostatic latent image. Developing means for developing a visible image by using the toner for transfer, transfer means for transferring the developed toner image onto a recording medium to form an unfixed image, and the unfixed image as the recording medium An image forming apparatus comprising a fixing unit for fixing to the image forming apparatus,
The image forming apparatus according to claim 1, wherein the image forming toner used to form the visible image is the image forming toner according to claim 1.   12. The image forming apparatus according to claim 11, wherein a conveyance speed of the recording medium at the time of fixing by the fixing unit is 280 mm / second or more. An image carrier;
A charging unit that charges the surface of the image carrier, an exposure unit that exposes the charged image carrier surface to form an electrostatic latent image, and develops the formed electrostatic latent image using image forming toner. At least one means selected from developing means, transfer means for transferring the developed toner image to a recording medium, and cleaning means for removing toner remaining on the surface of the image carrier after transfer;
Is a process cartridge that can be attached to and detached from the integrated image forming apparatus body,
7. A process cartridge according to claim 1, wherein the image forming toner used is the image forming toner according to claim 1.