JP2005091737A - Electrostatic charge image developing toner, developer, and image forming apparatus - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an electrostatic latent image developing toner which deals with a low-temperature fixing system and forms an image having good offset resistance and heat resistant preservable property and high quality while maintaining cleanability on a photoreceptor after transfer. <P>SOLUTION: The electrostatic latent image developing toner consists of at least a binder resin, a colorant and a release agent, and the weight average grain size of the toner is 3.0 to 6.0 μm. A shape coefficient SF-1 (A) and a content rate (B) (number %) of the fine powder of the grain size ≤3 μm satisfies equation 1: that is, 8≤B≤14 when 155≤A≤180, and 8≤B≤0.6A-79 when 145<A<155. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

  The present invention relates to a toner used as a developer for developing an electrostatic image in electrophotography, electrostatic recording, electrostatic printing and the like. More particularly, the present invention relates to a toner developer for developing an electrostatic image used in a copying machine, a laser printer, a plain paper fax machine, and the like using a direct or indirect electrophotographic developing system, and an image forming apparatus thereof.

  Conventionally, in an electrophotographic apparatus, an electrostatic recording apparatus, or the like, an electric or magnetic latent image is developed with toner. For example, in electrophotography, an electrostatic charge image (latent image) is formed on a photoreceptor, and then the latent image is developed with toner to form a toner image. The toner image is usually transferred onto a recording medium such as paper and then fixed by a method such as heating. Further, after the toner image is transferred, the toner remaining on the photoreceptor is removed by a cleaning blade or the like.

As a fixing method in electrophotography, a heated heat roller method is widely used because of its energy efficiency. Further, in recent years, the thermal energy given to the toner at the time of fixing tends to be small like low-temperature fixing and high-speed copying for energy saving. In particular, to save energy, the fixing unit is installed to shorten the waiting time (image warm-up time) from when the image forming device is turned on until image formation is possible, and to reach the fixable temperature quickly after a print command. There is a strong demand for reduction of total power consumption and CO ₂ emission by minimizing the amount of power used for preheating (preheating state).
The 1999 International Energy Agency (IEA) DSM (Demand-side Management) program includes a technology procurement project for next-generation copiers, the requirements for which were published, and for copiers of 30 cpm and above, It is required to drastically reduce the total power consumption and CO ₂ emissions compared to conventional copiers so that the standby time is within 10 seconds and the standby power consumption is 10-30W or less (differs depending on the copying speed). Has been. In particular, when the speed is increased, the heating member is deprived of heat by the recording medium at the time of fixing, so that the amount of heat necessary for fixing becomes insufficient, and further low-temperature fixing properties on both the fixing device and the toner are required.

On the other hand, after the transfer of the toner image, several methods have been studied as a method for sufficiently removing the toner remaining on the photosensitive member. However, a cleaning blade is brought into contact with the surface of the photosensitive member to scrape the residual toner. The dropping method is widely used because it is low-cost, the entire system is simple and compact, and the toner transfer efficiency is excellent.
The removal of residual toner as described above is performed by bringing the cleaning blade into contact with the surface of the photoconductor. Therefore, the toner removal efficiency depends on the contact pressure between the photoconductor and the cleaning blade, the developing sleeve, the surface shape of the photoconductor, and the like. It is greatly influenced. Similarly, in terms of toner characteristics, the toner removal efficiency during cleaning greatly depends on the toner shape and toner surface properties. When toner removal is insufficient, filming due to residual toner occurs on the surface of the photoreceptor. In addition, the stress applied between the photosensitive member and the cleaning blade increases due to the filming film accumulated in the film, thereby causing toner fusion due to heat generation and fatigue friction of the photosensitive member. This problem is further accelerated as the toner particle size is reduced, and the amount of toner passing between the photoconductor and the cleaning blade increases because the adhesion force to the photoconductor increases and the transfer residue tends to remain, resulting in more defective cleaning. There is a problem.

In order to overcome these problems, an image forming method (see, for example, Patent Document 1) in which the shape factor SF-1 of the toner particles is set to 125 to 140, and the particle size and SF-1 content is defined. In the blade brush cleaning method, control is performed so that the number of toner particles having a shape factor SF-1 in the range of 100 to 160 is 65% by number or more (see, for example, Patent Document 2), and the toner in the two-component developer is used. In order to accurately detect and replenish toner in the developer container, the shape factor SF-1 is 100 or more and 140 or less, SF-2 is 100 or more and 120 or less, and the specific resistance is 1 × 10 ¹⁰ Ω · cm. Using a magnetic carrier of 1 × 10 ¹⁴ Ω · cm or less (see, for example, Patent Document 3), the developing sleeve and the photosensitive member are driven in the same direction, and the peripheral speed ratio is 0.5 to 1.8. In case, The shape factor SF-1 is from 135 to 150, and the SF-2 is from 115 to 125 (see, for example, Patent Document 4). Furthermore, spherical particles and irregular particles are contained at a certain ratio. A mixed toner (for example, see Patent Document 5) is disclosed. These objectives are not limited to improving cleaning properties, but are proposals related to toner shape. In both cases, the shape factor of toner particles is set to solve image quality problems (mainly improved cleaning properties and transferability). Improvement).

JP 2000-267331 A JP 2002-23408 A JP 2000-29297 A JP-A-9-179411 JP 7-49585 A

  However, according to the present inventors, it has been found that in the range control of the shape factor (SF-1) as set in the prior art, the cleaning performance may be insufficient depending on the conditions of the blade cleaning method. Yes. For example, with respect to the toner particle side, particularly when the toner particle size becomes smaller or smaller as the toner particle size becomes smaller due to the recent increase in image quality, or when the toner surface property is smooth and unevenness is small, Regarding the forming apparatus side, when the contact pressure between the photosensitive member surface and the cleaning blade is relatively low and disadvantageous for cleaning, etc., the residual toner is insufficiently removed within the range of the shape factor defined in the prior art. The problem accompanying the above-mentioned cleaning defect will generate | occur | produce. In particular, toner particles having a small particle size have an increased adhesion to the photoconductor, so that the transfer remains on the photoconductor even after development, the cleaning member is easily consumed, and the mechanical stress is large. In addition, when the photosensitive member is contact-charged, there is a problem that the charging roller or the like is contaminated and the original charging ability cannot be exhibited. On the other hand, with the toner particles having a large particle size, the cleaning property is improved, but there is a problem that the transfer quality is deteriorated and the image quality such as the resolution is lowered due to this.

On the other hand, it is known that the cleaning failure largely depends on the difference in toner surface property. However, this difference in toner surface property is greatly influenced by the toner production methods such as the pulverization method and the polymerization method. is there.
The toner obtained by the conventional kneading and pulverization method is generally advantageous in terms of cleaning properties because it is indefinite, but its particle size distribution is broad, low fluidity, low transferability, fixing energy However, there is a problem that the charge amount is uneven among the toner particles and the charging stability is low. Particularly in fixing, a kneaded and pulverized toner produced by a pulverization method is cracked at the interface of a release agent (wax) by pulverization to form particles, so that there is a large amount on the particle surface, so a release effect is likely to occur. On the other hand, the adhesion to the carrier, the photosensitive member, and the cleaning blade easily occurs, and the performance is unsatisfactory.
On the other hand, in order to overcome the problems of the toner by the kneading and pulverizing method, a toner manufacturing method by the polymerization method has been proposed. Since this method does not include a pulverization step, the toner does not require a kneading step and a pulverization step, which contributes to cost savings such as energy saving, production time reduction, and product yield improvement. large. In addition, the particle size distribution in the polymerized toner particles obtained by such a polymerization method is easy to form a sharp distribution as compared with the particle size distribution of the toner by the pulverization method, and it is easy to encapsulate the wax. It is possible to greatly improve the performance. It is also easy to obtain a spherical toner. However, there are many problems that have not yet been solved in the toner produced by the polymerization method.

  In the production method of toner by suspension polymerization method widely used in the polymerization method, the monomer for binder (binder resin) used in the method is limited to styrene monomer and acrylic monomer which are harmful to human body. Since the toner to be contained contains these components, there is an environmental problem. In addition, since the obtained toner encapsulates the wax, when the toner is used in an actual machine, the adhesion of the toner to the photoreceptor is reduced. As a result, the wax hardly permeates the toner surface, resulting in a toner with poor fixing efficiency. Therefore, the polymerized toner becomes a disadvantageous toner for power consumption.

In addition to the suspension polymerization method, the polymerization toner production method includes an emulsion polymerization method. In the emulsion polymerization method, the monomer is limited to the styrene monomer. Also in this method, it is difficult to completely remove the unreacted monomer from the toner particles, and it is difficult to completely remove the emulsifier and the dispersant from the toner particles, which causes an environmental problem due to the toner.
Further, a dissolution suspension method is known as a toner production method. In this method, there is a merit that a polyester resin capable of low temperature fixing can be used, but since the high molecular weight component is added in the process of dissolving or dispersing the low temperature fixing resin and the colorant in the solvent, the liquid viscosity is increased and the productivity is increased. The problem comes to occur.
Furthermore, in this dissolution suspension method, the toner surface shape is spherical and the surface is made uneven to improve the cleaning of the toner (see, for example, Patent Document 6). When a wax is added to the composition as a release agent, the uniform dispersion of the wax, the dispersion state (surface presence), and the uniform dispersion of the pigment are lower than those of the kneading and pulverizing type toner. Since the degree of freedom in polymer design becomes particles in a solvent, there is a restriction on viscosity, which makes it difficult to secure releasability.

According to Patent Document 7, a practical sphericity composed of an elongation reaction product of a urethane-modified polyester as a toner binder for the purpose of improving toner fluidity, low-temperature fixability, and hot offset property is 0.90 to 1. 00 dry toner has been proposed. In addition, Patent Documents 8 and 9 disclose dry toners that are excellent in powder flowability and transferability in the case of a small particle size toner, and also excellent in all of heat-resistant storage stability, low-temperature fixability, and hot offset resistance. Has been described. The toner production methods described in these publications include a high molecular weight process in which an isocyanate group-containing polyester prepolymer is subjected to a polyaddition reaction with an amine in an aqueous medium.
However, although fixing, transferability, and fluidity are improved, since it is spherical, the cleaning property is greatly reduced as compared with the irregular toner of the pulverized toner. In addition, in the case of the toner obtained by the above-described method, the dispersion of the pigment and wax is poor, and the pigment is unevenly dispersed in the toner. Therefore, the image obtained with this toner has low transparency. The problem was that the saturation was inferior. Particularly in oilless fixing, there is a problem that a sufficient release width cannot be obtained because there is no dispersion control of the release agent and the oilless fixing toner is not designed.

JP 9-15903 A Japanese Patent Laid-Open No. 11-133665 JP-A-11-149180 JP 2000-292981 A

  The toner manufactured by the polymerization method as described above has high self-lubricating property because it has less irregularity on the surface shape, less sphericity and no large variation compared to the pulverized toner. For this reason, there has been a problem that it becomes easy to slip through the contact portion between the photosensitive member and the cleaning blade, and the occurrence of defective cleaning becomes more remarkable. Further, since there is a general tendency that the adhesion force to the surface of the photosensitive member tends to be strong, there is a problem that cleaning failure and image deterioration become more remarkable.

  Therefore, in view of the above problems, the present invention is compatible with a low-temperature fixing system while maintaining the cleaning property on the photoreceptor after transfer, and forms a high-quality image with good offset resistance and heat-resistant storage stability. It is an object of the present invention to provide a toner for developing an electrostatic charge image and an image forming apparatus using the same. Another object of the present invention is to provide a toner container filled with the toner, a developer containing the toner, an image forming method using the developer, and an image forming apparatus loaded with the developer in a developing device. To do.

In order to solve the above problems, the present invention is characterized by the following.
1. The present invention relates to a step of forming a toner image by attaching toner to an electrostatic charge image formed on an image carrier, a step of transferring the toner image onto a recording medium, and two fixing members disposed opposite to each other And a step of fixing the toner image on the recording medium by passing the recording medium between the toner and the untransferred toner remaining on the image carrier after the toner image transfer is cleaned by a cleaning member contacting the image carrier. A toner for developing an electrostatic charge image used in an image forming method comprising at least a binder resin, a colorant, and a release agent, wherein the toner has a weight average particle diameter of 3.0 to 6.0 μm. The toner for developing an electrostatic charge image satisfies the following formula 1 in which the shape factor SF-1: A of the toner and the fine powder content ratio B (number%) having a particle size of 3 μm or less are satisfied.
(Formula 1) When 155 ≦ A ≦ 180, 8 ≦ B ≦ 14
When 145 <A <155, 8 ≦ B ≦ 0.6 A−79

2. In the toner for developing an electrostatic charge image, the toner has an outflow start temperature measured by an elevated flow tester of 90 to 110 ° C.
3. In the electrostatic image developing toner, the fixing step of the image forming method is performed with a surface pressure (roller load / contact area) applied between the two fixing members being 1.5 × 10 ⁵ Pa or less. It is characterized by.
4). In the electrostatic image developing toner, the cleaning step of the image forming method is characterized by cleaning with an elastic rubber blade in contact with the rotation direction of the image carrier in the counter direction.

5). In the electrostatic image developing toner, the toner is a dissolved or dispersed product formed by dissolving or dispersing a toner composition containing a toner binder component made of a modified polyester resin (i) capable of reacting with active hydrogen in an organic solvent. Is reacted with a crosslinking agent and / or an extender in an aqueous medium containing resin fine particles, the solvent is removed from the obtained dispersion, and the resin fine particles adhering to the toner surface are washed and detached. It is characterized by.
6). In the electrostatic image developing toner, the modified polyester resin (i) is a modified polyester resin having a urea group.

7). In the electrostatic image developing toner, the toner binder component contains an unmodified polyester resin (LL) together with the modified polyester resin (i), and a weight ratio of (i) to (LL) [(i) / (LL)] is 5/95 to 80/20.
8). In the electrostatic image developing toner, the unmodified polyester resin (LL) has a peak molecular weight of 1000 to 20000.
9. In the electrostatic image developing toner, the acid value of the unmodified polyester resin (LL) is 10 to 30 mgKOH / g.
10. In the toner for developing an electrostatic image, the glass transition point (Tg) of the unmodified polyester resin (LL) is 35 to 55 ° C.

11. In the toner for developing an electrostatic charge image, the toner further contains a wax, the wax is finely dispersed in the toner, and is present in a state in which the wax is present more in the vicinity of the surface than in the central portion.
12 In the electrostatic image developing toner, the toner is characterized in that a charge control substance is fixed on the surface of toner base particles.
13. In the toner for developing an electrostatic charge image, the toner is obtained by volume shrinkage of 10 to 90% in an aqueous medium using a solid fine particle dispersant.
14 In the electrostatic image developing toner, the toner includes an organic solvent contained in a dispersion liquid in which at least fine droplet particles containing an organic solvent, a binder resin, and a colorant are dispersed in an aqueous medium containing resin fine particles. It is obtained by removing the solvent.

15. According to another aspect of the present invention, there is provided a toner container filled with any one of the above electrostatic charge image developing toners.
16. Furthermore, the present invention is characterized by containing any of the above-mentioned toners for developing an electrostatic image.
17. In addition, the present invention is a developing device in which any one of the above developers is loaded.
18. In addition, the present invention is an image forming method for developing an electrostatic image formed on an image carrier using any one of the above-described developers.

19. Further, the present invention provides an image carrier, an electrostatic image forming unit for forming an electrostatic image on the image carrier, and a developing unit for developing the electrostatic image formed on the image carrier with a developer containing toner. And a transfer means for transferring the toner image on the image carrier onto the recording medium, and a fixing means for fixing the toner image on the recording medium by passing the recording medium between two opposingly arranged fixing members. And an image forming apparatus comprising: a cleaning unit that cleans untransferred toner remaining on the image carrier after the toner image is transferred by a cleaning member that contacts the image carrier. Is an image forming apparatus.
20. In the image forming apparatus, the image carrier is an amorphous silicon photoconductor.
21. In the image forming apparatus, the developing unit applies an alternating electric field when developing the electrostatic image on the image carrier.

22. In the image forming apparatus, the fixing unit includes a heating body including a heating element, a film in contact with the heating body, and a pressure member in pressure contact with the heating body through the film. And a recording medium on which a toner image is transferred between the pressure member and the pressure member.
23. In the image forming apparatus, the charging unit performs charging by bringing a charging member into contact with the image carrier and applying a voltage to the charging member.

24. According to another aspect of the present invention, there is provided a process cartridge which is integrally supported including at least an image carrier and a developing unit, and is detachably formed on the main body of the image forming apparatus. This is a process cartridge.

  According to the present invention, the cleaning ability of the transfer residual toner is good, the deterioration of the cleaning blade, the photoreceptor, or the image quality caused by this is prevented, the low-temperature fixability is good, the offset resistance, the heat resistance An electrostatic charge image developing toner having excellent storage stability can be provided. Further, a high-quality image can be formed by a developer, a developing device, and an image forming apparatus using the electrostatic image developing toner.

Hereinafter, embodiments of the present invention will be described.
The inventors of the present invention have a process of forming a toner image by attaching toner to an electrostatic charge image formed on an image carrier, a process of transferring the toner image onto a recording medium, and two opposingly arranged processes. A step of fixing the toner image on the recording medium by passing the recording medium between the fixing members, and a cleaning member for contacting the untransferred toner remaining on the image carrier after the toner image transfer to the image carrier And an electrostatic charge image developing toner used in an image forming method including at least a cleaning step, wherein the toner has a particle size and a particle size of 3 μm or less in a toner composed of at least a binder resin, a colorant, and a release agent. It has been found that the content is largely related to the toner fixability, and at the same time, the toner has a shape factor SF-1: A, a fine powder content with a particle size of 3 μm or less: B (number%), Meet Thus, it has been found that sufficient fixability and cleanability can be ensured, no abnormal image is generated, and in addition to this, a high-quality image can be provided over a long period of time without transfer defects.
(Formula 1)
When 155 ≦ A ≦ 180, 8 ≦ B ≦ 14
When 145 <A <155, 8 ≦ B ≦ 0.6 A−79

The reason why the particle size of the toner and the content of the fine powder having a particle size of 3 μm or less influence the fixability of the toner is presumably because it affects the uniformity of the toner layer on the recording medium.
Focusing on the particle diameter of the toner, as a result of experiments by the present inventors, a toner having a weight average particle diameter of 3 to 6 μm and a fine powder content of 3 μm or less of 8% by number or more showed good fixability. When the weight average particle size is less than 3 μm, and when it is larger than 6 μm, and when the content of fine powder of 3 μm or less is less than 8% by number even if the weight average particle size is 3 to 6 μm, the fixing property is inferior. It was. The cause is that when the particle size and the content of fine powder of 3 μm or less are in the above range, the toner layer on the recording medium becomes uniform and heat conduction from the fixing member becomes uniform, so that the heat melting state of the toner becomes uniform. It is estimated that the toner is fixed on the recording medium. On the other hand, when the weight average particle size is less than 3 μm, particularly when the surface irregularities of the recording medium are large, heat and pressure from the fixing member are not sufficiently applied to the toner entering the recesses, and the fixability is poor. It may be enough. On the other hand, when the weight average particle diameter is larger than 6 μm, the uniformity of the toner layer is insufficient, and uniform heat may not be applied, resulting in insufficient fixability.

As described above, the cleaning property is greatly related to the toner shape and the surface property, but the amount of fine toner that easily passes through the cleaning blade is also greatly related to the cleaning property. Conversely, when the toner has a large particle diameter, image deterioration such as transfer failure occurs. Therefore, in order to ensure good cleaning properties and to suppress the occurrence of image deterioration such as transfer failure, it is necessary that the shape factor SF-1 and the fine powder content have a control range represented by the above (formula 1). Found in the invention.
According to the experiments by the present inventors, when the shape factor SF-1 of the toner is 145 or less, since the shape is round, a large amount of toner passes through the photosensitive member and the cleaning blade even if the amount of fine powder is small, resulting in poor cleaning. Occur. Further, when the shape factor SF-1 is 155 or more, it is considered that the larger the value of SF-1 is, the more advantageous the cleaning property is. However, since the amount of fine powder becomes a dominant factor for cleaning, the fine powder content is 3 μm or less. When it exceeds 14% by number, there are many slips from the cleaning blade, and the cleaning property cannot be maintained for a long time. Furthermore, when the value of SF-1 is more than 145 and less than 155, coexistence of the shape factor and the fine powder content is indispensable for ensuring the cleaning property, and the fine powder content of 3 μm or less is the above (formula 1 ) Must be satisfied.
As described above, when the content of fine powder of 3 μm or less is less than 8% by number, fixing failure occurs, which is not preferable. Further, when SF-1 is larger than 180, there is a problem in that the image quality is remarkably lowered due to a decrease in transfer rate, a change in toner shape during long-term image passing, particularly a pulverization and an increase in fine powder rate. This is not preferable.

The toner produced by the polymerization method is likely to produce particles with smooth surface irregularity, and there is a concern that the margin of cleaning performance will be lowered. However, satisfying the above conditions ensures sufficient cleaning performance it can.
The problems inherent to the developer and the image forming apparatus can be solved by producing the developer using the toner particles controlled as described above, or by mounting the developer on the image forming apparatus. . Specifically, in the case of a developer, heat generated by excessive stress applied between the photosensitive member and the cleaning blade may cause spent on the carrier due to toner fusion, thereby solving the problem that the chargeability decreases with time. it can. Further, in the case of an image forming apparatus, it is possible to solve the deterioration of the cleaning blade due to poor cleaning, the deterioration of the photosensitive member, or the image quality deterioration caused by this.

(Measurement method of fine powder content of 3 μm or less, volume average particle size, shape factor SF-1)
An outline of a Coulter counter and a flow type particle image apparatus used for measuring particles in the present invention is shown. The volume average particle size was measured by connecting a number distribution and volume distribution interface (manufactured by Nikka) and a PC9801 personal computer (manufactured by NEC) to a Coulter Counter TA-II manufactured by Coulter Electronics, USA. The electrolyte was adjusted to a 1% NaCl aqueous solution using primary sodium chloride. As a measuring method, 0.1 to 5 ml of a surfactant, preferably alkylbenzene sulfonate, is added as a dispersant to 50 to 100 ml of the electrolytic solution, and 1 to 10 mg of a sample is added. This is subjected to a dispersion treatment for 1 minute with an ultrasonic disperser, 100 to 200 ml of an electrolytic aqueous solution is put into another beaker, the sample dispersion is added to a predetermined concentration therein, and the Coulter Counter TA- Measure the particle size distribution of 30000 particles of 2 to 40 μm on the basis of the number using a 100 μm aperture as type II aperture, calculate the volume distribution and number distribution of 2 to 40 μm particles, and fine powder with a particle size of 3 μm or less The content and the volume average particle diameter (Dv: the median value of each channel is the representative value of the channel) were determined.

The toner shape factor SF-1 in the present invention is expressed by the following (Equation 2), and indicates the degree of the spherical shape of the toner particles.
Shape factor (SF-1) = ((absolute maximum length of toner particles) ² / projection area of toner particles) × (π / 4) × 100 (Equation 2)
It means that the calculated SF-1 value is deformed from a spherical shape to an indefinite shape as the value increases from 100. Here, (absolute maximum length of toner particles) refers to the absolute maximum length of a parallel line interval when a projected image of toner particles on a plane is sandwiched between two parallel lines. Further, (projected area of toner particles) refers to the area of the projected image of the toner particles on the plane.
The toner shape factor SF-1 is measured so that a toner image enlarged by 1000 times magnification using a scanning electron microscope SEM (S-2700) manufactured by Hitachi, Ltd. has a particle count of about 100 (or more). This is a procedure for extracting the image information, introducing the image information into an image analysis apparatus (LuzexAP) manufactured by Nireco Co., Ltd. via an interface, performing analysis, and obtaining the shape factor SF-1 calculated from the above equation. In the present invention, as described above, when SF-1 is small, the toner easily passes through the photosensitive member and the cleaning blade, so that a cleaning failure is likely to occur. In addition, when SF-1 is relatively large, 180 or more, the cleaning property is good, but generally, the transfer efficiency is lowered and the image quality deterioration such as transfer white spot occurs.

(Flow tester measurement)
As a flow tester, for example, there is an elevated flow tester CFT500 type manufactured by Shimadzu Corporation. The flow curve based on the data from the flow tester is in a state as shown in FIGS. 1A and 1B, and each temperature can be read therefrom. In the figure, Ts is the softening temperature, Tfb is the outflow start temperature, and the melting temperature in the 1/2 method is the T1 / 2 temperature. The conditions in the flow tester are preferably 5 kg, a die of 1.0 mm, and an outflow start point range of 90 to 110 ° C. obtained at a temperature increase of 3 ° C./min. When the temperature is 90 ° C. or lower, the hot offset is lowered, and when the temperature is 110 ° C. or higher, the fine particle polymer on the surface layer is inhibited to lower the fixing property.
<Measurement conditions>
Load: 5 kg / cm ² , temperature rising rate: 3.0 ° C./min,
Die diameter: 1.0 mm, die length: 10.0 mm

(Fixing device)
Next, the configuration of the fixing device of the image forming apparatus in which the electrostatic image developing toner of the present invention is used will be described. FIG. 2 is a schematic configuration diagram of the fixing device according to the present invention. In this figure, 71 is a fixing roller, 72 is a pressure roller, 71a is a metal cylinder, 71b is an offset prevention layer, 71c is a heating lamp, 72a is a metal cylinder, 72b is an offset prevention layer, 72c is a heating lamp, and T is a toner. An image S represents a recording medium.
In the fixing device having such a configuration, the surface pressure (roller load / contact area) applied between the two rollers is fixed to 1.5 × 10 ⁵ Pa or less. The conventional surface pressure exceeds 1.5 × 10 ⁵ Pa, otherwise it cannot be sufficiently fixed. In contrast, the toner of the present invention can be fixed even at a low temperature, and can be fixed even at a low surface pressure of 1.5 × 10 ⁵ Pa or less. Further, since the surface pressure is reduced, the toner image on the recording medium is not crushed and disturbed, so that a high-definition image can be output.

(Static image developing toner)
As a method for producing the toner for developing an electrostatic charge image of the present invention, known means such as a pulverization method and a polymerization method can be used, but any method is acceptable as long as the produced toner falls within the scope of the claims. May be used. However, the toner produced by the polymerization method is less prone to surface irregularities and is likely to be poorly cleaned. In the present invention, a polymerized toner is used for the purpose of aiming at a particle size distribution with little variation and stabilization of chargeability. Details of the polymerized toner used in the present embodiment will be described below.

[Modified polyester resin (i)]
The modified polyester resin (i) in the present invention is a polyester resin in which a functional group contained in an acid or alcohol monomer unit and a bonding group other than an ester bond are present, or a resin component having a different configuration is present in the polyester resin. It has a structure bonded by a covalent bond, an ionic bond or the like.
For example, a polyester terminal is reacted with something other than an ester bond, specifically, a functional group such as an acid group or an isocyanate group that reacts with a hydroxyl group is introduced into the terminal, and further reacted with an active hydrogen-containing compound. Those that have been modified or extended are also included. Further, compounds having a plurality of active hydrogen groups include those in which polyester ends are bonded to each other (such as urea-modified polyester and urethane-modified polyester).
In addition, a reactive group such as a double bond is introduced into the polyester main chain, radical polymerization is introduced therefrom, a carbon-carbon bond graft component is introduced into the side chain, or double bonds are bridged together. (Styrene-modified, acrylic-modified polyester, etc.).
Also, a polyester resin in which a resin component having a different structure is copolymerized in the main chain of the polyester or reacted with a carboxyl group or a hydroxyl group at the end, for example, a silicone resin having a terminal modified with a carboxyl group, a hydroxyl group, an epoxy group, or a mercapto group And those copolymerized with (silicone-modified polyester, etc.). This will be specifically described below.

[Synthesis example of polystyrene-modified polyester resin (i)]
Into a reaction vessel equipped with a cooling pipe, a stirrer and a nitrogen introduction pipe, 724 parts by weight of bisphenol A ethylene oxide 2-mole adduct, 200 parts by weight of isophthalic acid and 70 parts by weight of fumaric acid, and 2 parts by weight of dibutyltin oxide are added. The mixture was reacted at 230 ° C. for 8 hours and further at a reduced pressure of 10 to 15 mmHg for 5 hours, then cooled to 160 ° C., 32 parts by weight of phthalic anhydride was added thereto and reacted for 2 hours. Next, the mixture was cooled to 80 ° C., 200 parts by weight of styrene, 1 part by weight of benzoyl peroxide and 0.5 parts by weight of dimethylaniline were added in ethyl acetate, and the reaction was performed for 2 hours. A polystyrene graft-modified polyester resin (i) having a molecular weight of 92,000 was obtained.

[Urea-modified polyester resin (i)]
Examples of the urea-modified polyester (i) include a reaction product of a polyester prepolymer (A) having an isocyanate group and an amine (B). Examples of the polyester prepolymer (A) having an isocyanate group include a polycondensate of a polyol (1) and a polycarboxylic acid (2), and a polyester having an active hydrogen group further reacted with a polyisocyanate (3). Is mentioned. Examples of the active hydrogen group possessed by the polyester include hydroxyl groups (alcoholic hydroxyl groups and phenolic hydroxyl groups), amino groups, carboxyl groups, mercapto groups, and the like. Among these, alcoholic hydroxyl groups are preferred.

Examples of the polyol (1) include a diol (1-1) and a tri- or higher valent polyol (1-2). (1-1) alone or (1-1) and a small amount of (1-2) Mixtures are preferred.
Diol (1-1) includes alkylene glycol (ethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, 1,4-butanediol, 1,6-hexanediol, etc.); alkylene ether glycol (diethylene glycol) , Triethylene glycol, dipropylene glycol, polyethylene glycol, polypropylene glycol, polytetramethylene ether glycol, etc.); alicyclic diols (1,4-cyclohexanedimethanol, hydrogenated bisphenol A, etc.); bisphenols (bisphenol A, bisphenol) F, bisphenol S, etc.); alkylene oxide (ethylene oxide, propylene oxide, butylene oxide, etc.) adduct of the above alicyclic diol; Alkylene oxide phenol compound (ethylene oxide, propylene oxide, butylene oxide, etc.), etc. adducts. Among them, preferred are alkylene glycols having 2 to 12 carbon atoms and alkylene oxide adducts of bisphenols, and particularly preferred are alkylene oxide adducts of bisphenols and alkylene glycols having 2 to 12 carbon atoms. It is a combined use.

  The trihydric or higher polyol (1-2) includes 3 to 8 or higher polyhydric aliphatic alcohols (glycerin, trimethylolethane, trimethylolpropane, pentaerythritol, sorbitol, etc.); trihydric or higher phenols (Trisphenol PA, phenol novolak, cresol novolak, etc.); and alkylene oxide adducts of the above trivalent or higher polyphenols.

Examples of the polycarboxylic acid (2) include dicarboxylic acid (2-1) and trivalent or higher polycarboxylic acid (2-2). (2-1) alone and (2-1) with a small amount of ( The mixture of 2-2) is preferred.
Dicarboxylic acid (2-1) includes alkylene dicarboxylic acid (succinic acid, adipic acid, sebacic acid, etc.); alkenylene dicarboxylic acid (maleic acid, fumaric acid, etc.); aromatic dicarboxylic acid (phthalic acid, isophthalic acid, terephthalic acid) And naphthalenedicarboxylic acid). Of these, preferred are alkenylene dicarboxylic acids having 4 to 20 carbon atoms and aromatic dicarboxylic acids having 8 to 20 carbon atoms.

  Examples of the trivalent or higher polycarboxylic acid (2-2) include aromatic polycarboxylic acids having 9 to 20 carbon atoms (trimellitic acid, pyromellitic acid, and the like). In addition, as polycarboxylic acid (2), you may make it react with polyol (1) using the acid anhydride or lower alkyl ester (methyl ester, ethyl ester, isopropyl ester, etc.) of the above-mentioned thing.

  The ratio of the polyol (1) to the polycarboxylic acid (2) is usually 2/1 to 1/1, preferably 1. as the equivalent ratio [OH] / [COOH] of the hydroxyl group [OH] and the carboxyl group [COOH]. 5/1 to 1/1, more preferably 1.3 / 1 to 1.02 / 1.

  Examples of the polyisocyanate (3) include aliphatic polyisocyanates (tetramethylene diisocyanate, hexamethylene diisocyanate, 2,6-diisocyanatomethylcaproate, etc.); alicyclic polyisocyanates (isophorone diisocyanate, cyclohexylmethane diisocyanate, etc.); aromatic Diisocyanates (tolylene diisocyanate, diphenylmethane diisocyanate, etc.); araliphatic diisocyanates (α, α, α ′, α′-tetramethylxylylene diisocyanate, etc.); isocyanurates; polyisocyanates such as phenol derivatives, oximes, caprolactams, etc. And a combination of two or more of these.

  The ratio of the polyisocyanate (3) is usually 5/1 to 1/1, preferably 4 /, as an equivalent ratio [NCO] / [OH] of the isocyanate group [NCO] and the hydroxyl group [OH] of the polyester having a hydroxyl group. 1 to 1.2 / 1, more preferably 2.5 / 1 to 1.5 / 1. When [NCO] / [OH] exceeds 5, low-temperature fixability deteriorates. If the molar ratio of [NCO] is less than 1, the urea content in the modified polyester will be low, and the hot offset resistance will deteriorate.

The content of the polyisocyanate (3) component in the polyester prepolymer (A) having an isocyanate group at the terminal is usually 0.5 to 40% by weight, preferably 1 to 30% by weight, more preferably 2 to 20% by weight. %. If it is less than 0.5% by weight, the hot offset resistance deteriorates, and it is disadvantageous in terms of both heat-resistant storage stability and low-temperature fixability. On the other hand, if it exceeds 40% by weight, the low-temperature fixability deteriorates.
The number of isocyanate groups contained per molecule in the polyester prepolymer (A) having an isocyanate group is usually 1 or more, preferably 1.5 to 3 on average, more preferably 1.8 to 2.5 on average. It is a piece. If it is less than 1 per molecule, the molecular weight of the modified polyester resin (i) becomes low, and the hot offset resistance deteriorates.

As amines (B), diamine (B1), triamine or higher polyamine (B2), amino alcohol (B3), amino mercaptan (B4), amino acid (B5), and amino groups of (B1) to (B5) (B6) etc. that are blocked.
Examples of the diamine (B1) include aromatic diamines (phenylenediamine, diethyltoluenediamine, 4,4′-diaminodiphenylmethane, etc.); alicyclic diamines (4,4′-diamino-3,3′-dimethyldicyclohexylmethane, diamines). Cyclohexane, isophoronediamine, etc.); and aliphatic diamines (ethylenediamine, tetramethylenediamine, hexamethylenediamine, etc.) and the like.

Examples of the trivalent or higher polyamine (B2) include diethylenetriamine and triethylenetetramine. Examples of amino alcohol (B3) include ethanolamine and hydroxyethylaniline. Examples of amino mercaptan (B4) include aminoethyl mercaptan and aminopropyl mercaptan. Examples of the amino acid (B5) include aminopropionic acid and aminocaproic acid.
As (B6) which blocked the amino group of (B1) to (B5), ketimine compounds obtained from the amines and ketones (acetone, methyl ethyl ketone, methyl isobutyl ketone, etc.) of (B1) to (B5), Examples include oxazoline compounds. Among these amines (B), preferred are (B1) and a mixture of (B1) and a small amount of (B2).

  Furthermore, if necessary, the molecular weight of the modified polyester resin (i) can be adjusted using an elongation terminator. Examples of the elongation terminator include monoamines (diethylamine, dibutylamine, butylamine, laurylamine, etc.), and those obtained by blocking them (ketimine compounds).

  The ratio of amines (B) is equivalent to the equivalent ratio [NCO] / [NHx] of isocyanate groups [NCO] in the polyester prepolymer (A) having isocyanate groups and amino groups [NHx] in amines (B). Is usually 1/2 to 2/1, preferably 1.5 / 1 to 1 / 1.5, more preferably 1.2 / 1 to 1 / 1.2. When [NCO] / [NHx] exceeds 2 or less than 1/2, the molecular weight of the urea-modified polyester resin (i) becomes low, and the hot offset resistance deteriorates. In the present invention, the modified polyester resin (i) may contain a urethane bond together with a urea bond. The molar ratio of the urea bond content to the urethane bond content is usually 100/0 to 10/90, preferably 80/20 to 20/80, and more preferably 60/40 to 30/70. When the molar ratio of the urea bond is less than 10%, the hot offset resistance is deteriorated.

  The modified polyester resin (i) of the present invention is produced by a one-shot method or a prepolymer method. The weight average molecular weight of the modified polyester resin (i) is usually 10,000 or more, preferably 20,000 to 10,000,000, more preferably 30,000 to 1,000,000. If it is less than 10,000, the hot offset resistance deteriorates. The number average molecular weight of the modified polyester resin (i) is not particularly limited when the unmodified polyester resin (LL) described later is used, and may be a number average molecular weight that can be easily obtained to obtain the weight average molecular weight. . In the case of the modified polyester resin (i) alone, the number average molecular weight is usually 20000 or less, preferably 1000 to 10000, more preferably 2000 to 8000. When it exceeds 20000, the low-temperature fixability and the glossiness when used in a full-color apparatus are deteriorated.

[Unmodified polyester resin (LL)]
In the present invention, not only the modified polyester resin (i) is used alone, but also the unmodified polyester resin (LL) can be contained as a toner binder resin component together with the (i). The combined use of (LL) improves low-temperature fixability and gloss when used in a full-color device, and is preferable to single use. Examples of (LL) include the same polycondensates of polyol (1) and polycarboxylic acid (2) as in the above-mentioned polyester component (i), and preferred ones are also the same as (i). Further, it is preferable that (i) and (LL) are at least partially compatible with each other in terms of low-temperature fixability and hot offset resistance. Accordingly, the polyester component (i) and the polyester component (LL) preferably have similar compositions. The weight ratio of (i) to (LL) in the case of containing (LL) is usually 5/95 to 80/20, preferably 5/95 to 30/70, more preferably 5/95 to 25/75, Particularly preferred is 7/93 to 20/80. When the weight ratio of (i) is less than 5%, the hot offset resistance is deteriorated, and it is disadvantageous in terms of both heat-resistant storage stability and low-temperature fixability.

The peak molecular weight of the unmodified polyester resin (LL) is usually 1000 to 20000, preferably 1500 to 10000, and more preferably 2000 to 8000. If it is less than 1000, heat-resistant storage stability will deteriorate, and if it exceeds 10,000, low-temperature fixability will deteriorate.
The hydroxyl value of (LL) is preferably 5 mgKOH / g or more, more preferably 10 to 120 mgKOH / g, and particularly preferably 20 to 80 mgKOH / g. If it is less than 5, it is disadvantageous in terms of both heat-resistant storage stability and low-temperature fixability. The acid value of (LL) is preferably 10 to 30 mg KOH / g. By giving an acid value, it tends to be negatively charged, and the fixability tends to be further improved.

  In the present invention, the glass transition point (Tg) of the unmodified polyester resin (LL) is usually 35 to 55 ° C, preferably 40 to 55 ° C. This makes it possible to achieve both heat-resistant storage stability and low-temperature fixability of the toner. Due to the coexistence of the modified polyester resin (i), the dry toner of the present invention tends to have good heat-resistant storage stability even when the glass transition point is low, as compared with known polyester toners.

In the present invention, as the storage elastic modulus of the toner binder resin, the temperature (TG ′) at which the measurement frequency is 20 Hz is 10000 dyne / cm ² is usually 100 ° C. or higher, preferably 110 to 200 ° C. If it is less than 100 ° C., the resistance to hot offset deteriorates. As the viscosity of the toner binder resin, the temperature (Tη) at 1000 poise at a measurement frequency of 20 Hz is usually 180 ° C. or lower, preferably 90 to 160 ° C. If it exceeds 180 ° C., the low-temperature fixability deteriorates. That is, TG ′ is preferably higher than Tη from the viewpoint of achieving both low temperature fixability and hot offset resistance. In other words, the difference between TG ′ and Tη (TG′−Tη) is preferably 0 ° C. or higher. More preferably, it is 10 degreeC or more, Most preferably, it is 20 degreeC or more. The upper limit of the difference is not particularly limited. Further, from the viewpoint of achieving both heat-resistant storage stability and low-temperature fixability, the difference between Tη and Tg is preferably 0 to 100 ° C. More preferably, it is 10-90 degreeC, Most preferably, it is 20-80 degreeC.

(Coloring agent)
As the colorant of the 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, Bengala, Red Tan, Lead Zhu, Cadmium Red, Cadmium Mercury Red, Antimony Zhu, Permanent Red 4R , Para red, phissa red, parac Lortho Nitroaniline Red, Resol Fast Scarlet G, Brilliant Fast Scarlet, Brilliant Carnmin 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, Pigment Scarlet 3B, Bordeaux 5B, Tolujing 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, Pi Lazolone Red, Polyazo Red, Chrome Vermilion, Benzidine Orange, 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, Indance Ren Blue (RS, BC), Indigo, Ultramarine Blue, Bituminous Blue, Anthraquinone Blue, Fast Violet B, Methyl Violet Lake, Cobalt Purple, Manganese Purple, Dioxane Violet, Anthraquinone Violet, Chrome Green, Zinc Green, Chrome Oxide, Pyridian, Emerald Green , Pigment Green B, Naphthol Green B, Green Gold, Acid Green Lake, Malachite Grits Nreki, phthalocyanine green, anthraquinone green, titanium oxide, zinc white, lithopone and mixtures thereof can be used. The content of the colorant is usually 1 to 15% by weight, preferably 3 to 10% by weight, based on the toner.

  The colorant used in the present invention can also be used as a master batch combined with a resin. In addition to the modified or unmodified polyester resins mentioned above, the binder resin kneaded together with the production of the masterbatch or the masterbatch is not limited to polystyrene, poly-p-chlorostyrene, polyvinyltoluene, or other styrene and its substitutes. Copolymer: Styrene-p-chlorostyrene copolymer, styrene-propylene copolymer, styrene-vinyltoluene copolymer, styrene-vinylnaphthalene copolymer, styrene-methyl acrylate copolymer, styrene-ethyl acrylate copolymer Polymer, styrene-butyl acrylate copolymer, styrene-octyl acrylate copolymer, styrene-methyl methacrylate copolymer, styrene-ethyl methacrylate copolymer, styrene-butyl methacrylate copolymer, styrene- α-chloromethacrylate Polymer, Styrene-acrylonitrile copolymer, Styrene-vinyl methyl ketone copolymer, Styrene-butadiene copolymer, Styrene-isoprene copolymer, Styrene-acrylonitrile-indene copolymer, Styrene-maleic acid copolymer, Styrene -Styrene copolymers such as maleic acid ester copolymers; polymethyl methacrylate, polybutyl methacrylate, polyvinyl chloride, polyvinyl acetate, polyethylene, polypropylene, polyester, epoxy resin, epoxy polyol resin, polyurethane, polyamide, polyvinyl butyral , Polyacrylic acid resin, rosin, modified rosin, terpene resin, aliphatic or alicyclic hydrocarbon resin, aromatic petroleum resin, chlorinated paraffin, paraffin wax, etc. Can be used.

  The masterbatch can be obtained by mixing and kneading a masterbatch resin and a colorant under high shear. In this case, an organic solvent can be used in order to enhance the interaction between the colorant and the resin. A so-called flushing method, which is a method of mixing and kneading an aqueous paste containing water of a colorant together with a resin and an organic solvent, transferring the colorant to the resin side, and removing water and organic solvent components, is also preferably used. Since the colorant wet cake can be used as it is, there is no need to dry it. For mixing and kneading, a high shear dispersion device such as a three-roll mill is preferably used.

(wax)
The toner of the present invention can also contain a wax together with the toner binder resin and the colorant. As a result of investigations by the present inventors, it has been clarified that the state of wax in the toner greatly affects the releasability of the toner at the time of fixing, and the wax is finely dispersed in the toner and is present inside the toner. As a result, it was clarified that a good fixing releasability can be obtained by the presence in the vicinity of the surface. In particular, it is preferable that the wax has a long diameter and is dispersed to 1 μm or less. However, when a large amount of wax is exposed on the toner surface, long-term agitation inside the developing device causes the wax to easily come off from the toner surface, adheres to the carrier surface, or adheres to the surface of the member in the developing device. Since the charge amount of the agent may be lowered, it is not preferable. The dispersion of these waxes is judged from an enlarged photograph obtained using a transmission electron microscope.

  Known waxes can be used, and examples thereof include polyolefin waxes (polyethylene wax, polypropylene wax, etc.); long-chain hydrocarbons (paraffin wax, sazol wax, etc.); carbonyl group-containing waxes, and the like. Of these, carbonyl group-containing waxes are preferred. Carbonyl group-containing waxes include polyalkanoic acid esters (carnauba wax, montan wax, trimethylolpropane tribehenate, pentaerythritol tetrabehenate, pentaerythritol diacetate dibehenate, glycerin tribehenate, 1,18 -Octadecanediol distearate, etc.); polyalkanol esters (tristearyl trimellitic acid, distearyl maleate, etc.); polyalkanoic acid amides (ethylene diamine dibehenyl amide, etc.); polyalkylamides (trimellitic acid tristearyl amide, etc.) And dialkyl ketones (such as distearyl ketone). Among these carbonyl group-containing waxes, polyalkanoic acid esters are preferred.

  The melting point of the wax used in the present invention is usually 40 to 160 ° C, preferably 50 to 120 ° C, more preferably 60 to 90 ° C. A wax having a melting point of less than 40 ° C. has an adverse effect on heat resistant storage stability, and a wax having a melting point of more than 160 ° C. tends to cause a cold offset when fixing at a low temperature. Further, the melt viscosity of the wax is preferably 5 to 1000 cps, more preferably 10 to 100 cps as a measured value at a temperature 20 ° C. higher than the melting point. Waxes exceeding 1000 cps have poor effects for improving hot offset resistance and low-temperature fixability. The content of the wax in the toner is usually 0 to 40% by weight, preferably 3 to 30% by weight.

(Charge control agent)
The toner of the present invention may contain a charge control substance as necessary. In particular, a high charge amount can be imparted by fixing the charge control substance to the surface of the toner. That is, by fixing the toner on the surface of the toner, the amount and state of presence on the toner surface are stabilized, and the charge amount can be stabilized. In particular, the stability of the charge amount is increased in the toner having the configuration of the present invention.
As the charge control substance, all known substances can be used. For example, nigrosine dyes, triphenylmethane dyes, chromium-containing metal complex dyes, molybdate chelate pigments, rhodamine dyes, alkoxy amines, quaternary ammonium salts (fluorine-modified) Quaternary ammonium salts), alkylamides, phosphorus simple substances or compounds, tungsten simple substances or compounds, fluorine-based activators, salicylic acid metal salts, and metal salts of salicylic acid derivatives.
Specifically, Nitronine dye Bontron 03, quaternary ammonium salt Bontron P-51, metal-containing azo dye Bontron S-34, oxynaphthoic acid metal complex E-82, salicylic acid metal complex E- 84, E-89 of a phenol-based condensate (manufactured by Orient Chemical Industry Co., Ltd.), TP-302 of a quaternary ammonium salt molybdenum complex, TP-415 (manufactured by Hodogaya Chemical Industry Co., Ltd.), quaternary ammonium Copy charge PSY VP2038 of salt, copy blue PR of triphenylmethane derivative, copy charge NEG VP2036 of quaternary ammonium salt, copy charge NX VP434 (manufactured by Hoechst), LRA-901, LR-147 which is a boron complex (Nippon Carlit), copper phthalocyanine, perylene, quinacridone, Examples thereof include azo pigments and other polymer compounds having a functional group such as a sulfonic acid group, a carboxyl group, and a quaternary ammonium salt.

  In the present invention, the amount of charge control agent used is determined uniquely by the type of binder resin, the presence or absence of additives used as necessary, and the toner production method including the dispersion method, and is uniquely limited. However, it is preferably used in the range of 0.1 to 10 parts by weight with respect to 100 parts by weight of the binder resin. The range of 0.2 to 5 parts by weight is preferable. When the amount exceeds 10 parts by weight, the chargeability of the toner is too high, the effect of the main charge control agent is reduced, the electrostatic attractive force with the developing roller is increased, the flowability of the developer is reduced, and the image density is reduced. Incurs a decline.

  These charge control agents and mold release agents can be melt-kneaded together with the master batch and the resin, and of course, they may be added when dissolved and dispersed in an organic solvent.

(Resin fine particles)
As the resin fine particles used in the present invention, any resin can be used as long as it can form an aqueous dispersion, and it may be a thermoplastic resin or a thermosetting resin. Examples of such resins include vinyl resins, polyurethane resins, epoxy resins, polyester resins, polyamide resins, polyimide resins, silicon resins, phenol resins, melamine resins, urea resins, aniline resins, ionomer resins, and polycarbonate resins. Is mentioned. The resin fine particles may be a combination of two or more of the above resins. Among these, those made of a vinyl resin, a polyurethane resin, an epoxy resin, a polyester resin, and a resin using a combination thereof are preferable because an aqueous dispersion of fine spherical resin particles is easily obtained.
The vinyl resin is a polymer obtained by homopolymerization or copolymerization of a vinyl monomer, such as a styrene- (meth) acrylic acid ester resin, a styrene-butadiene copolymer, a (meth) acrylic acid-acrylic acid ester polymer, Examples include styrene-acrylonitrile copolymers, styrene-maleic anhydride copolymers, styrene- (meth) acrylic acid copolymers, and the like. The average particle diameter of the resin fine particles is 5 to 2000 nm, preferably 20 to 300 nm.

(External additive)
As the external additive for assisting the fluidity, developability and chargeability of the colored particles obtained in the present invention, inorganic fine particles can be preferably used. The primary particle diameter of the inorganic fine particles is preferably 5 mμ to 2 μm, and particularly preferably 5 mμ to 500 mμ. Moreover, it is preferable that the specific surface area by BET method is 20-500 m < ² > / g. The proportion of the inorganic fine particles used is preferably 0.01 to 5% by weight of the toner, and particularly preferably 0.01 to 2.0% by weight. Specific examples of the inorganic fine particles include, for example, silica, alumina, titanium oxide, barium titanate, magnesium titanate, calcium titanate, strontium titanate, zinc oxide, tin oxide, quartz sand, clay, mica, wollastonite, diatomaceous earth. Examples include soil, chromium oxide, cerium oxide, bengara, antimony trioxide, magnesium oxide, zirconium oxide, barium sulfate, barium carbonate, calcium carbonate, silicon carbide, and silicon nitride.

  In addition, polymer fine particles, such as polystyrene obtained by soap-free emulsion polymerization, suspension polymerization, and dispersion polymerization, methacrylate esters, acrylate copolymers, polycondensation systems such as silicone, benzoguanamine, and nylon, thermosetting Examples thereof include polymer particles made of a resin.

  Such 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. .

  Further, as a cleaning property improver for removing the developer after transfer remaining on the photosensitive member or the primary transfer medium, for example, fatty acid metal salts such as zinc stearate and calcium stearate, such as polymethyl methacrylate fine particles, polystyrene fine particles, etc. Examples thereof include fine polymer particles produced by soap-free emulsion polymerization. The polymer fine particles preferably have a relatively narrow particle size distribution and a volume average particle size of 0.01 to 1 μm.

(Production method)
Examples of the method for producing the toner for developing an electrostatic charge image according to the present invention will be described below, but the present invention is not limited thereto.
The toner binder resin can be produced by the following method.
The polyol (1) and the polycarboxylic acid (2) are heated to 150 to 280 ° C. in the presence of a known esterification catalyst such as tetrabutoxytitanate or dibutyltin oxide, and the generated water is distilled off as necessary. Thus, a polyester having a hydroxyl group is obtained. Subsequently, at 40-140 degreeC, this is made to react with polyisocyanate (3), and the polyester prepolymer (A) which has an isocyanate group is obtained. Further, the polyester prepolymer (A) is reacted with amines (B) at 0 to 140 ° C. to obtain a modified polyester resin (i).
When reacting (3) and reacting (A) and (B), a solvent may be used as necessary. Usable solvents include aromatic solvents (toluene, xylene, etc.); ketones (acetone, methyl ethyl ketone, methyl isobutyl ketone, etc.); esters (ethyl acetate, etc.); amides (dimethylformamide, dimethylacetamide, etc.) and ethers And those inert to the isocyanate (3), such as tetrahydrofuran (such as tetrahydrofuran).
When the unmodified polyester resin (LL) is used in combination, (LL) is produced by the same method as that for the polyester having a hydroxyl group, and this is dissolved and mixed in the solution after completion of the reaction (i).

(Melting and kneading method)
Toner components such as a toner binder resin containing a modified polyester resin (i), a charge control agent and a pigment are mechanically mixed. This mixing step may be performed under normal conditions using a normal mixer with rotating wings, and is not particularly limited.
When the above mixing process is completed, the mixture is then charged into a kneader and melt-kneaded. As the melt kneader, a uniaxial or biaxial continuous kneader or a batch kneader using a roll mill can be used. It is important that the melt-kneading be performed under appropriate conditions so as not to cause the molecular chains of the toner binder resin to be broken. Specifically, the melt kneading temperature should be performed with reference to the softening point of the toner binder resin. If the temperature is too lower than the softening point, cutting is severe, and if the temperature is too high, dispersion does not proceed.

  When the above melt-kneading process is completed, the kneaded product is then pulverized. In this pulverization step, it is preferable to first coarsely pulverize and then finely pulverize. At this time, a method of pulverizing by colliding with a collision plate in a jet stream or pulverizing with a narrow gap between a rotor and a stator that rotate mechanically is preferably used.

After the pulverization step is completed, the pulverized product is classified in an air stream by centrifugal force or the like, thereby producing a toner having a predetermined particle size, for example, an average particle size of 5 to 20 μm.
Further, when preparing the toner, in order to improve the fluidity, storage stability, developability, and transferability of the toner, the hydrophobic silica fine powder and the like mentioned above are further added to the toner manufactured as described above. Add and mix inorganic fine particles. For mixing external 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 external additive, the external additive may be added midway or gradually. Of course, you may change the rotation speed of a mixer, rolling speed, time, temperature, etc. A strong load may be given first, then a relatively weak load, and 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, a Henschel mixer, and the like.

  In order to spheroidize the obtained toner, a toner material composed of a toner binder resin and a colorant is melt-kneaded and then finely pulverized and then mechanically spheronized using a hybridizer, mechano-fusion, etc. Examples thereof include a method of obtaining a spherical toner by dissolving and dispersing a toner material called a dry method in a solvent in which a toner binder is soluble and then removing the solvent using a spray drying apparatus. Moreover, although the method of making it spherical by heating in an aqueous medium is mentioned, it is not limited to this.

(Toner production method in aqueous medium)
The aqueous medium used in the present invention may be water alone, or a solvent miscible with water may be used in combination. Examples of the miscible solvent include alcohol (methanol, isopropanol, ethylene glycol, etc.), dimethylformamide, tetrahydrofuran, cellosolves (methylcellosolve, etc.), lower ketones (acetone, methyl ethyl ketone, etc.) and the like.
The toner particles may be formed by reacting a dispersion made of a polyester prepolymer (A) having an isocyanate group in an aqueous medium with (B), or using a modified polyester resin (i) produced in advance. Also good.
As a method for stably forming a dispersion comprising a modified polyester resin (i) or a polyester prepolymer (A) in an aqueous medium, the dispersion comprises a modified polyester resin (i) or a polyester prepolymer (A) in an aqueous medium. Examples thereof include a method of adding a toner raw material composition and dispersing it by shearing force. The colorant, colorant masterbatch, wax, charge control agent, unmodified polyester resin (LL), etc., which are polyester prepolymer (A) and other toner compositions (hereinafter referred to as toner raw materials) are dispersed in an aqueous medium. It may be mixed when the body is formed, but it is more preferable to mix the toner raw materials in advance and then add and disperse the mixture in the aqueous medium. In the present invention, other toner materials such as a colorant, a wax, and a charge control agent do not necessarily have to be mixed when forming particles in an aqueous medium, but are added after the particles are formed. May be. For example, after forming particles that do not contain a colorant, the colorant can be added by a known dyeing method.

(Solid fine particle dispersant)
Further, by adding a solid fine particle dispersant in advance to the aqueous medium, the dispersion of oil droplets in the aqueous phase is made uniform. This is because the solid fine particle dispersant is arranged on the surface of the oil droplets at the time of dispersion, and the dispersion of the oil droplets is made uniform, and at the same time, coalescence of the oil droplets is prevented and the particle size distribution is sharp. Toner can be obtained.
The solid fine particle dispersant is present in a solid state hardly soluble in water in an aqueous medium, and is preferably inorganic fine particles having an average particle diameter of 0.01 to 1 μm. Specific examples of the inorganic fine particles include, for example, silica, alumina, titanium oxide, barium titanate, magnesium titanate, calcium titanate, strontium titanate, zinc oxide, tin oxide, quartz sand, clay, mica, wollastonite, diatomaceous earth. Examples include soil, chromium oxide, cerium oxide, bengara, antimony trioxide, magnesium oxide, zirconium oxide, barium sulfate, barium carbonate, calcium carbonate, silicon carbide, and silicon nitride. More preferably, tricalcium phosphate, calcium carbonate, colloidal titanium oxide, colloidal silica, hydroxyapatite and the like can also be used. In particular, hydroxyapatite synthesized by reacting sodium phosphate and calcium chloride in water under basic conditions is preferable.

  The dispersion method is not particularly limited, and known equipment such as a low-speed shear method, a high-speed shear method, a friction method, a high-pressure jet method, and an ultrasonic wave can be applied. In order to make the particle size of the dispersion 2 to 20 μm, a high-speed shearing type is preferable. When a high-speed shearing disperser is used, the rotational speed is not particularly limited, but is usually 1000 to 30000 rpm, preferably 5000 to 20000 rpm. The dispersion time is not particularly limited, but in the case of a batch method, it is usually 0.1 to 5 minutes. The temperature during dispersion is usually 0 to 150 ° C. (under pressure), preferably 40 to 98 ° C. Higher temperatures are preferred in that the dispersion made of the modified polyester resin (i) or the prepolymer (A) has a low viscosity and is easily dispersed.

  The amount of the aqueous medium used is usually 50 to 2000 parts by weight, preferably 100 to 1000 parts by weight, based on 100 parts by weight of the toner composition containing the modified polyester resin (i) and the prepolymer (A). If the amount is less than 50 parts by weight, the dispersion state of the toner composition is poor, and toner particles having a predetermined particle diameter cannot be obtained. If it exceeds 20000 parts by weight, it is not economical. Moreover, a dispersing agent can also be used as needed. It is preferable to use a dispersant because the particle size distribution becomes sharp and the dispersion is stable.

  As a dispersant for emulsifying and dispersing the oily phase in which the toner composition is dispersed in an aqueous medium, an anionic surfactant such as alkylbenzene sulfonate, α-olefin sulfonate, and phosphate ester, alkylamine salt, Amino alcohol fatty acid derivatives, polyamine fatty acid derivatives, amine salt types such as imidazoline, and quaternary alkyltrimethylammonium salts, dialkyldimethylammonium salts, alkyldimethylbenzylammonium salts, pyridinium salts, alkylisoquinolinium salts, benzethonium chloride, etc. Nonionic surfactants such as ammonium salt type cationic surfactants, fatty acid amide derivatives, polyhydric alcohol derivatives such as alanine, dodecyldi (aminoethyl) glycine, di (octylaminoethyl) glycine and N-alkyl-N, - amphoteric surfactants, such as dimethyl ammonium betaine and the like.

  Further, by using a surfactant having a fluoroalkyl group, the effect can be obtained in a very small amount. Preferred anionic surfactants having a fluoroalkyl group include fluoroalkyl carboxylic acids having 2 to 10 carbon atoms and metal salts thereof, disodium perfluorooctanesulfonyl glutamate, 3- [omega-fluoroalkyl (C6-C11 ) Oxy] -1-alkyl (C3-C4) sodium sulfonate, 3- [omega-fluoroalkanoyl (C6-C8) -N-ethylamino] -1-propanesulfonic acid sodium, fluoroalkyl (C11-C20) carvone Acids and metal salts thereof, perfluoroalkylcarboxylic acids (C7 to C13) and metal salts thereof, perfluoroalkyl (C4 to C12) sulfonic acids and metal salts thereof, perfluorooctanesulfonic acid diethanolamide, N-propyl-N- (2-hydroxye B) Perfluorooctanesulfonamide, perfluoroalkyl (C6-C10) sulfonamidopropyltrimethylammonium salt, perfluoroalkyl (C6-C10) -N-ethylsulfonylglycine salt, monoperfluoroalkyl (C6-C16) ethyl phosphate Examples include esters.

  Product names include Surflon S-111, S-112, S-113 (Asahi Glass Co., Ltd.), Florard FC-93, FC-95, FC-98, FC-129 (Sumitomo 3M Co., Ltd.), Unidyne DS-101. DS-102 (manufactured by Taikin Kogyo Co., Ltd.), Mega-Fac F-l10, F-120, F-113, F-191, F-812, F-833 (Dainippon Ink Co., Ltd.), Xtop EF-102 , 103, 104, 105, 112, 123A, 123B, 306A, 501, 201, 204 (manufactured by Tochem Products), and Fgentent F-100, F150 (manufactured by Neos).

  Examples of the cationic surfactant include aliphatic primary, secondary or tertiary amine acids having a fluoroalkyl group, and aliphatic quaternary ammonium salts such as perfluoroalkyl (C6-C10) sulfonamidopropyltrimethylammonium salts. Benzalkonium salt, benzethonium chloride, pyridinium salt, imidazolinium salt, trade names include Surflon S-121 (Asahi Glass), Florard FC-135 (Sumitomo 3M), Unidyne DS-202 (Daikin Industries) ), Megafuck F-150, F-824 (Dainippon Ink Co., Ltd.), Xtop EF-132 (Tochem Products Co., Ltd.), Footgent F-300 (Neos Co., Ltd.) and the like.

  Further, the dispersed droplets may be stabilized by a polymer protective colloid. For example, acrylic acid, methacrylic acid, α-cyanoacrylic acid, α-cyanomethacrylic acid, itaconic acid, crotonic acid, fumaric acid, maleic acid or maleic anhydride and other (meth) acrylic monomers containing hydroxyl groups Such as β-hydroxyethyl acrylate, β-hydroxyethyl methacrylate, β-hydroxypropyl acrylate, β-hydroxypropyl methacrylate, γ-hydroxypropyl acrylate, γ-hydroxypropyl methacrylate, 3-chloroacrylate 2-hydroxypropyl, 3-chloro-2-hydroxypropyl methacrylate, diethylene glycol monoacrylate, diethylene glycol monomethacrylate, glycerol monoacrylate, glycerol monomethacrylate, N -Methylol acrylamide, N-methylol methacrylamide, etc., vinyl alcohol or ethers with vinyl alcohol, such as vinyl methyl ether, vinyl ethyl ether, vinyl propyl ether, etc., or esters of compounds containing vinyl alcohol and carboxyl groups, such as Vinyl acetate, vinyl propionate, vinyl butyrate, etc., acrylamide, methacrylamide, diacetone acrylamide or their methylol compounds, acid chlorides such as acrylic acid chloride, methacrylic acid chloride, vinyl pyridine, vinyl pyrrolidone, vinyl imidazole, ethylene imine, etc. Homopolymers or copolymers such as those having a nitrogen atom or a heterocyclic ring thereof, polyoxyethylene, polyoxypropylene, Oxyethylene alkylamine, polyoxypropylene alkylamine, polyoxyethylene alkylamide, polyoxypropylene alkylamide, polyoxyethylene nonyl phenyl ether, polyoxyethylene lauryl phenyl ether, polyoxyethylene stearyl phenyl ester, polyoxyethylene nonylphenyl Polyoxyethylenes such as esters, celluloses such as methyl cellulose, hydroxyethyl cellulose, and hydroxypropyl cellulose can be used.

  In addition, when an acid such as calcium phosphate salt or an alkali-soluble substance is used as the dispersion stabilizer, the calcium phosphate salt is dissolved from the fine particles by a method such as dissolving the calcium phosphate salt with an acid such as hydrochloric acid and washing with water. Remove. It can also be removed by operations such as enzymatic degradation.

  When a dispersant is used, the dispersant may remain on the surface of the toner particles, but it is preferable from the charged surface of the toner that the dispersant is washed and removed after the elongation and / or crosslinking reaction.

Furthermore, in order to lower the viscosity of the toner composition, a solvent in which the modified polyester resin (i) or the polyester prepolymer (A) is soluble can be used. The use of a solvent is preferable in that the particle size distribution becomes sharp. The solvent is preferably volatile with a boiling point of less than 100 ° C. from the viewpoint of easy removal. Examples of the solvent include toluene, xylene, benzene, carbon tetrachloride, methylene chloride, 1,2-dichloroethane, 1,1,2-trichloroethane, trichloroethylene, chloroform, monochlorobenzene, dichloroethylidene, methyl acetate, ethyl acetate, Methyl ethyl ketone, methyl isobutyl ketone and the like can be used alone or in combination of two or more. In particular, aromatic solvents such as toluene and xylene and halogenated hydrocarbons such as methylene chloride, 1,2-dichloroethane, chloroform, and carbon tetrachloride are preferable.
The usage-amount of the solvent with respect to 100 weight part of polyester prepolymers (A) is 0-300 weight part normally, Preferably it is 0-100 weight part, More preferably, it is 25-70 weight part. When a solvent is used, it is removed by heating under normal pressure or reduced pressure after elongation and / or crosslinking reaction.

  The elongation and / or crosslinking reaction time is selected depending on the reactivity of the isocyanate group structure of the polyester prepolymer (A) and the amines (B), but is usually 10 minutes to 40 hours, preferably 2 to 24 hours. It is. The reaction temperature is generally 0 to 150 ° C, preferably 40 to 98 ° C. Moreover, a well-known catalyst can be used as needed. Specific examples include dibutyltin laurate and dioctyltin laurate.

In order to obtain the desired shape of the toner, before removing the solvent from the obtained dispersion liquid after the elongation and / or crosslinking reaction, the dispersion liquid is sheared into a stirring tank equipped with a homomixer, an Ebara milder, and a stirrer. Using a device that applies force, the particles having a substantially spherical shape are deformed into a spindle shape, and then the particles are immobilized by providing a step of removing the solvent from the dispersion at a Tg or less of the binder resin, so that the desired It becomes possible to produce a toner having a shape of 1.
Examples of the method for adjusting the shearing force include the treatment time and number of treatments of the apparatus, the temperature and viscosity of the dispersion, and the concentration of the organic solvent in the particles. Also, the particles themselves have different shapes depending on the coverage of the resin fine particles on the surface of the particles, the degree of reactivity with the compound having an active hydrogen group, etc., and the degree of deformation due to the shearing force varies.

  In order to remove the organic solvent from the obtained emulsified dispersion, a method in which the temperature of the entire system is gradually raised to completely evaporate and remove the organic solvent in the droplets can be employed. Alternatively, the emulsified dispersion can be sprayed into a dry atmosphere to completely remove the water-insoluble organic solvent in the droplets to form toner fine particles, and the aqueous dispersant can be removed by evaporation together. . As a dry atmosphere in which the emulsified dispersion is sprayed, a gas obtained by heating air, nitrogen, carbon dioxide gas, combustion gas, or the like, in particular, various air currents heated to a temperature equal to or higher than the boiling point of the highest boiling solvent used is generally used. A spray dryer, belt dryer, rotary kiln, etc. can provide the desired quality in a short time.

In addition, in order to control the toner shape, it is important to use a solid fine particle dispersant in a production method having a volume shrinkage step with a volume shrinkage of 10 to 90% in an aqueous medium. Here, the volume shrinkage ratio is Vo, which is the volume of the oil phase (dispersed phase) in which the toner composition before being emulsified and dispersed in the aqueous medium is dispersed, and Vt is the volume of the dispersed phase after emulsified and dispersed to remove volatile components. As described above, volumetric shrinkage ratio = (1−Vt / Vo) × 100, and changes in characteristics before emulsification and after being emulsified and dispersed are measured.
Specifically, it can be determined by the following method.
(1) A method of measuring the weight and true specific gravity of the oil phase before emulsification and the obtained toner.
(2) A method of measuring the average particle diameter of the droplets after emulsification and dispersion in an aqueous medium and particles from which volatile components have been removed, and converting the average particle size.
If the volume shrinkage is out of the range of 10 to 90%, the particle shape becomes indefinite, which is not preferable. Moreover, a more preferable range is 30 to 70%.

When the particle size distribution at the time of emulsification dispersion is wide and washing and drying processes are performed while maintaining the particle size distribution, the particle size distribution can be adjusted by classifying into a desired particle size distribution. In the classification operation, the fine particle portion can be removed in the liquid by a cyclone, a decanter, centrifugation, or the like. Of course, the classification operation may be performed after obtaining the powder as a powder after drying. The unnecessary fine particles or coarse particles obtained can be returned to the kneading step and used for the formation of particles. At that time, fine particles or coarse particles may be wet.
The dispersant used is preferably removed from the obtained dispersion as much as possible, but it is preferable to carry out it simultaneously with the classification operation described above.

The surface of the resulting powder after drying is mixed with different types of particles such as wax as release agent, charge control agent, fluidizing agent, colorant, etc., and mechanical impact force is applied to the mixed powder. It is possible to prevent detachment of foreign particles from the surface of the resulting composite particles by immobilizing and fusing.
Specific means include a method of applying an impact force to the mixture by blades rotating at high speed, a method of injecting and accelerating the mixture in a high-speed air stream, and causing particles or composite particles to collide with an appropriate collision plate, etc. is there. As equipment, Ong mill (manufactured by Hosokawa Micron Co., Ltd.), I-type mill (manufactured by Nippon Pneumatic Co., Ltd.) has been modified to reduce the pulverization air pressure, hybridization system (manufactured by Nara Machinery Co., Ltd.), kryptron System (manufactured by Kawasaki Heavy Industries, Ltd.), automatic mortar, etc.

(Developer)
When the toner of the present invention is used for a two-component developer, it may be used by mixing with a magnetic carrier, and the content ratio of the carrier and the toner in the developer is 1 to 10 weights of toner with respect to 100 parts by weight of the carrier. Part is preferred. As the magnetic carrier, conventionally known ones such as iron powder, ferrite powder, magnetite powder, magnetic resin carrier having a particle diameter of about 20 to 200 μm can be used.
The carrier may be coated with a resin, and examples of the coating material include amino resins such as urea-formaldehyde resin, melamine resin, benzoguanamine resin, urea resin, polyamide resin, and epoxy resin. Polyvinyl and polyvinylidene resins such as 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 Fluoro such as terpolymers of Kka vinylidene and a non-fluorinated monomer, and silicone resins.

Moreover, you may make conductive powder etc. contain in coating resin as needed. As the conductive powder, metal powder, carbon black, titanium oxide, tin oxide, zinc oxide or the like can be used. These conductive powders preferably have an average particle diameter of 1 μm or less. When the average particle diameter is larger than 1 μm, it becomes difficult to control electric resistance.
The toner of the present invention can also be used as a one-component magnetic toner that does not use a carrier or a non-magnetic toner.

  An embodiment of an image forming apparatus provided with a developing device according to the present invention will be described below with reference to FIG. FIG. 3 shows a cross section of the image forming apparatus. A charging roller 2 for charging a uniform charge on the photosensitive drum 1 in proximity to or in contact with the periphery of the photosensitive drum 1 as an image carrier, and the photosensitive member. An exposure device 3 that is an exposure means for forming an electrostatic latent image on the drum 1, a developing device 4 that visualizes the electrostatic latent image to form a toner image, a transfer belt 6 that transfers the toner image onto a sheet, and photosensitive A cleaning device 8 that removes residual toner on the photosensitive drum 1, a static elimination lamp 9 that neutralizes residual charges on the photosensitive drum 1, and an optical sensor 10 for controlling the charging roller applied voltage and developer toner concentration are disposed. ing.

  As the photosensitive drum 1, an amorphous silicon photosensitive member is preferably used. Amorphous silicon photoconductors are obtained by heating a conductive support to 50 to 400 ° C. and forming a vacuum deposition method, a sputtering method, an ion plating method, a thermal CVD method, a photo CVD method, a plasma CVD method, or the like on the support. It can be manufactured by forming a photoconductive layer made of amorphous silicon (hereinafter referred to as “a-Si”) by a film method. Among them, a plasma CVD method, that is, a method in which a source gas is decomposed by direct current, high frequency or microwave glow discharge to form an a-Si deposited film on a support is preferably used.

  The layer structure of the amorphous silicon photoconductor is, for example, as follows. FIG. 4 is a schematic diagram for explaining the layer structure. A photoconductor 500 shown in FIG. 4A is provided with a photoconductive layer 502 made of a-Si: H, X and having photoconductivity on a support 501. A photoconductor 500 shown in FIG. 4B includes a photoconductive layer 502 made of a-Si: H, X and having photoconductivity on a support 501, and an a-Si based surface layer 503. ing. A photoconductor 500 shown in FIG. 4C has a photoconductive layer 502 made of a-Si: H, X and having photoconductivity, an a-Si based surface layer 503, and a- And a Si-based charge injection blocking layer 504. A photoconductor 500 shown in FIG. 4D is provided with a photoconductive layer 502 on a support 501. The photoconductive layer 502 includes a charge generation layer 505 made of a-Si: H, X and a charge transport layer 506, on which an a-Si based surface layer 503 is provided.

The support 501 of the photoreceptor 500 may be conductive or electrically insulating. Examples of the conductive support include metals such as Al, Cr, Mo, Au, In, Nb, Te, V, Ti, Pt, Pd, and Fe, and alloys thereof such as stainless steel. Also, at least the surface on the side where the photosensitive layer is to be formed of an electrically insulating support such as polyester, polyethylene, polycarbonate, cellulose acetate, polypropylene, polyvinyl chloride, polystyrene, polyamide or other synthetic resin film or sheet, glass or ceramic. A conductively treated support can also be used.
The shape of the support 501 can be a smooth surface, a cylindrical or plate-like surface having an uneven surface, or an endless belt, and the thickness thereof is appropriately determined so that a desired photoreceptor for an image forming apparatus can be formed. However, when flexibility as a photoreceptor for an image forming apparatus is required, it can be made as thin as possible within a range in which the function as a support can be sufficiently exhibited. However, the support is usually 10 μm or more from the viewpoints of manufacturing and handling, such as mechanical strength.

In the amorphous silicon photoconductor, a charge injection blocking layer 504 having a function of blocking charge injection from the conductive support side is provided between the conductive support 501 and the photoconductive layer 502 as needed. It is effective (FIG. 4C). That is, the charge injection blocking layer 504 has a function of blocking charge injection from the support 501 side to the photoconductive layer 502 side when the photosensitive layer is subjected to a charging process having a constant polarity on its free surface. It has a so-called polarity dependency in which such a function is not exhibited when it is subjected to a charging process with a reverse polarity. In order to provide such a function, the charge injection blocking layer 504 contains a relatively large number of atoms for controlling conductivity as compared with the photoconductive layer 502.
The thickness of the charge injection blocking layer 504 is preferably 0.1 to 5 [mu] m, more preferably 0.3 to 4 [mu] m, and most preferably 0.5 in view of obtaining desired electrophotographic characteristics and economic effects. It is desirable that the thickness be ˜3 μm.

  The photoconductive layer 502 is formed on the undercoat layer as necessary, and the layer thickness of the photoconductive layer 502 is appropriately determined as desired from the viewpoints of obtaining desired electrophotographic characteristics and economic effects. Is preferably 1 to 100 μm, more preferably 20 to 50 μm, and most preferably 23 to 45 μm.

The charge transport layer 506 is a layer mainly having a function of transporting charges when the photoconductive layer 502 is functionally separated. The charge transport layer 506 includes at least silicon atoms, carbon atoms, and fluorine atoms as constituent elements, and is formed of a-SiC (H, F, O) including hydrogen atoms and oxygen atoms as required. Photoconductive properties, particularly charge retention properties, charge generation properties, and charge transport properties. In the present invention, it is particularly preferable to contain an oxygen atom.
The layer thickness of the charge transport layer 506 is appropriately determined as desired from the viewpoint of obtaining desired electrophotographic characteristics and economic effects. The charge transport layer is preferably 5 to 50 μm, more preferably 10 to 40 μm. Optimally, the thickness is desirably 20 to 30 μm.

The charge generation layer 505 is a layer mainly having a function of generating charges when the photoconductive layer 502 is functionally separated. This charge generation layer 505 is composed of a-Si: H containing at least silicon atoms as components and substantially not containing carbon atoms, and if necessary containing hydrogen atoms, and has desired photoconductive properties, particularly charge generation. Characteristics and charge transport characteristics.
The layer thickness of the charge generation layer 505 is appropriately determined as desired from the viewpoint of obtaining desired electrophotographic characteristics and economic effects, etc., preferably 0.5 to 15 μm, more preferably 1 to 10 μm, optimally 1 to 5 μm.

If necessary, the amorphous silicon photoconductor 500 can be further provided with a surface layer 503 on the photoconductive layer 502 formed on the support 501 as described above. It is preferable to form a layer. The surface layer 503 has a free surface and is provided to achieve the object of the present invention mainly in moisture resistance, continuous repeated use characteristics, electrical pressure resistance, use environment characteristics, and durability.
The thickness of the surface layer 503 in the present invention is usually 0.01 to 3 μm, preferably 0.05 to 2 μm, and most preferably 0.1 to 1 μm. If the layer thickness is less than 0.01 μm, the surface layer is lost due to wear or the like during use of the photoreceptor 500, and if it exceeds 3 μm, electrophotographic characteristics such as an increase in residual potential are observed.

  The amorphous silicon photoconductor has a high surface hardness, high sensitivity to long wavelength light such as a semiconductor laser (770 to 800 nm) and the like, and hardly deteriorated by repeated use. It can be suitably used for electrophotographic photoreceptors such as (LBP).

Next, the developing device 4 will be described.
The developing device 4 is loaded with the developer of the present invention. The developing device 4 is supplied with toner from a toner supply device (not shown) through a toner supply port.
In the developing device 4, during development, an oscillating bias voltage in which an AC voltage is superimposed on a DC voltage is applied to the developing sleeve 4a as a developing bias from a power source (not shown). The background portion potential and the image portion potential are located between the maximum value and the minimum value of the vibration bias potential. As a result, an alternating electric field whose direction changes alternately is formed in the developing portion. In this alternating electric field, the toner and carrier of the developer vibrate vigorously, and the toner flies off the photosensitive sleeve 1 while shaking off the electrostatic restraining force on the developing sleeve 4a and the carrier, corresponding to the latent image on the photosensitive drum 1. And adhere.
The difference (maximum peak voltage) between the maximum value and the minimum value of the vibration bias voltage is preferably 0.5 to 5 kV, and the frequency is preferably 1 to 10 kHz. As the waveform of the vibration bias voltage, a rectangular wave, a sine wave, a triangular wave, or the like can be used. As described above, the DC voltage component of the vibration bias is a value between the background part potential and the image part potential, but the value closer to the background part potential than the image part potential is more likely to cover the background part potential region. This is preferable for preventing toner adhesion.
When the vibration bias voltage waveform is a rectangular wave, the duty ratio is preferably 50% or less. Here, the duty ratio is a ratio of time during which the toner is directed to the photosensitive drum 1 during one cycle of the vibration bias. By doing so, it is possible to increase the difference between the peak value at which the toner is directed to the photosensitive drum 1 and the time average value of the bias, so that the movement of the toner is further activated and the toner is transferred to the latent image surface. It is possible to improve the rough feeling and the resolution by adhering faithfully to the potential distribution. Further, since the difference between the peak value at which the carrier having the charge opposite to that of the toner is directed to the photosensitive drum 1 and the time average value of the bias can be reduced, the movement of the carrier is calmed down and the latent image The probability that the carrier adheres to the background portion can be greatly reduced.

Next, the cleaning device 8 will be described.
In the present invention, if a cleaning step is performed by the cleaning blade 8 made of an elastic rubber blade that comes into contact with the rotation direction of the photosensitive drum 1 in the counter direction, paper dust and filming on the photosensitive drum 1 are further reduced. It is preferable because it can be effectively removed. The elastic rubber blade is preferably configured to have a free end on the support member, but is not limited thereto. The elastic rubber blade has a hardness of JIS A 60-70 °, rebound resilience 30-70%, Young's modulus 30-60 kgf / cm ² , thickness 1.5-3.0 mm, free length 7-12 mm, photoconductor The pressing force to the drum 1 is 15 g / cm or less, and the contact angle of the elastic rubber blade to the photosensitive drum 1 is 5 ° to 50 °, preferably 10 ° to 30 °.

The image forming operation is performed as follows.
The photosensitive drum 1 rotates counterclockwise. The photosensitive drum 1 is neutralized by the neutralizing light 9, and the surface potential is averaged to a reference potential of 0 to -150V. Next, it is charged by the charging roller 2 and the surface potential becomes about -1000V. Next, the surface potential of the portion (image portion) that is exposed by the exposure device 3 and irradiated with light is 0 to −200V. The toner on the sleeve 4a adheres to the image portion by the developing device 4. The photosensitive drum 1 on which the toner image is formed rotates and moves, and the paper is fed from the paper feeding unit 5 at a timing such that the front end of the paper and the front end of the image coincide with each other with the transfer belt 6. The toner image on the surface of the drum 1 is transferred to the paper. Thereafter, the sheet is sent to the fixing unit 7 where the toner is fused to the sheet by heat and pressure and discharged as a copy. The fixing unit 7 may be a fixing device composed of a fixing roller and a pressure roller as described above.
The residual toner remaining on the photosensitive drum 1 is scraped off by the cleaning blade 8, and the toner is recycled through the toner supply port (not shown). After that, the photosensitive drum 1 is neutralized by the neutralizing light 9 to be in an initial state where there is no toner, and the process proceeds to the next image forming process again.

FIG. 5 is a diagram showing a schematic configuration of the process cartridge according to the present invention.
In FIG. 5, reference numeral 100 denotes the entire process cartridge, 101 denotes a photoreceptor, 102 denotes charging means, 103 denotes developing means, and 104 denotes cleaning means. The developing means 103 is loaded with the developer of the present invention. In the present invention, the process cartridge 100 is integrally supported including at least the photosensitive member 101 and the developing unit 103, and is formed to be detachable from a main body of an image forming apparatus such as a copying machine or a printer. As shown in FIG. 5, components such as charging device means 102 and cleaning means 104 may be included.
This process cartridge is a process cartridge that is compatible with a low-temperature fixing system while maintaining cleanability on the photosensitive member 101, and also has good offset resistance and heat-resistant storage stability.

  EXAMPLES The present invention will be further described below with reference to examples, but the present invention is not limited thereto. In addition, a part shows a weight part.

<Example 1>
(Synthesis of organic fine particle emulsion)
In a reaction vessel equipped with a stirrer and a thermometer, 683 parts of water, 11 parts of sodium salt of ethylene oxide methacrylate adduct sulfate (Eleminol RS-30, manufactured by Sanyo Chemical Industries), 83 parts of styrene, 83 parts of methacrylic acid, When 110 parts of butyl acrylate and 1 part of ammonium persulfate were added and stirred at 400 rpm for 15 minutes, a white emulsion was obtained. The system was heated to raise the system temperature to 75 ° C. and reacted for 5 hours. Further, 30 parts of a 1% ammonium persulfate aqueous solution was added, and the mixture was aged at 75 ° C. for 5 hours, and an aqueous vinyl resin (a copolymer of styrene-methacrylic acid-butyl acrylate-methacrylic acid ethylene oxide adduct sulfate sodium salt). A dispersion [fine particle dispersion 1] was obtained. The volume average particle diameter of [Fine Particle Dispersion 1] measured with LA-920 was 0.10 μm. A portion of [Fine Particle Dispersion 1] was dried to isolate the resin component. The resin content Tg was 57 ° C.

(Preparation of aqueous phase)
990 parts of water, 80 parts of [fine particle dispersion 1], 40 parts of 48.5% aqueous solution of sodium dodecyl diphenyl ether disulfonate (Eleminol MON-7: Sanyo Chemical Industries) and 90 parts of ethyl acetate are mixed and stirred to give a milky white liquid. Got. This is designated as [Aqueous Phase 1].

(Synthesis of low molecular weight polyester)
In a reaction vessel equipped with a condenser, a stirrer and a nitrogen inlet tube, 220 parts of bisphenol A ethylene oxide 2-mole adduct, 561 parts of bisphenol A propylene oxide 3-mole adduct, 218 parts of terephthalic acid, 48 parts of adipic acid and dibutyl Add 2 parts of tin oxide, react for 8 hours at 230 ° C. under normal pressure, and further react for 5 hours under reduced pressure of 10-15 mmHg, then add 45 parts of trimellitic anhydride into the reaction vessel and add 2 parts at 180 ° C. under normal pressure. The reaction was performed for a while to obtain [Low molecular weight polyester 1]. [Low molecular weight polyester 1] had a number average molecular weight of 2500, a weight average molecular weight of 6700, a Tg of 43 ° C., and an acid value of 25 mgKOH / g.

(Synthesis of polyester prepolymer)
In a reaction vessel equipped with a condenser, a stirrer and a nitrogen introduction tube, 682 parts of bisphenol A ethylene oxide 2-mole adduct, 81 parts of bisphenol A propylene oxide 2-mole adduct, 283 parts of terephthalic acid, 22 parts of trimellitic anhydride And 2 parts of dibutyltin oxide were added, reacted at 230 ° C. under normal pressure for 8 hours, and further reacted for 5 hours at a reduced pressure of 10 to 15 mmHg to obtain [Intermediate Polyester 1]. [Intermediate Polyester 1] had a number average molecular weight of 2,100, a weight average molecular weight of 9,500, Tg of 55 ° C., an acid value of 0.5, and a hydroxyl value of 49.
Next, 411 parts of [Intermediate polyester 1], 89 parts of isophorone diisocyanate, and 500 parts of ethyl acetate are placed in a reaction vessel equipped with a cooling tube, a stirrer and a nitrogen introduction tube, and reacted at 100 ° C. for 5 hours. Polymer 1] was obtained. [Prepolymer 1] had a free isocyanate weight% of 1.53%.

(Synthesis of ketimine)
In a reaction vessel equipped with a stirrer and a thermometer, 170 parts of isophoronediamine and 75 parts of methyl ethyl ketone were charged and reacted at 50 ° C. for 5 hours to obtain [ketimine compound 1]. The amine value of [ketimine compound 1] was 418.

(Synthesis of master batch)
Carbon black (Cabot Co., Ltd. Regal 400R): 40 parts, Binder resin: Polyester resin (Sanyo Kasei RS-801; acid value 10, Mw 20000, Tg 64 ° C.): 60 parts, water: 30 parts are mixed in a Henschel mixer. A mixture in which water was soaked into the pigment aggregate was obtained. This was kneaded for 45 minutes with two rolls set at a roll surface temperature of 130 ° C. and pulverized to a size of 1 mmφ with a pulverizer to obtain [Masterbatch 1].

(Production of oil phase)
In a container equipped with a stir bar and a thermometer, 378 parts of [Low molecular weight polyester 1], 110 parts of Carnauba WAX, 22 parts of a charge control agent (salicylic acid metal complex E-84: manufactured by Orient Chemical Industry), 947 parts of ethyl acetate are charged. The temperature was raised to 80 ° C. with stirring, maintained at 80 ° C. for 5 hours, and then cooled to 30 ° C. in 1 hour. Next, 500 parts of [Masterbatch 1] and 500 parts of ethyl acetate were charged in a container and mixed for 1 hour to obtain [Raw material solution 1].
[Raw material solution 1] 1324 parts were transferred to a container, and using a bead mill (Ultra Visco Mill; manufactured by Imex Corporation), a liquid feed speed of 1 kg / hr, a disk peripheral speed of 6 m / sec, and 0.5 mm zirconia beads were 80% by volume. Carbon black and WAX were dispersed under conditions of filling and 3 passes. Next, 1324 parts of a 65% ethyl acetate solution of [low molecular weight polyester 1] was added, followed by one pass with a bead mill under the above conditions to obtain [Pigment / WAX Dispersion 1]. The solid content concentration of [Pigment / WAX Dispersion 1] (130 ° C., 30 minutes) was 50%.

(Emulsification)
[Pigment / WAX Dispersion 1] 648 parts, [Prepolymer 1] 154 parts, [Ketimine Compound 1] 6.6 parts in a container and TK homomixer (manufactured by Tokushu Kika) at 5,000 rpm for 1 minute After mixing, 1200 parts of [Aqueous phase 1] was added to the container, and mixed with a TK homomixer at 13,000 rpm for 20 minutes to obtain [Emulsion slurry 1].

(Variation)
1365 parts of ion-exchanged water, 35 parts of carboxymethyl cellulose (CMC Daicel-1280: manufactured by Daicel Chemical Industries, Ltd.) in an aqueous solution stirred and mixed with 1000 parts of [Emulsion slurry 1], and TK homomixer (special machine) For 1 hour at 2,000 rpm to obtain [Deformed slurry 1].

(Solvent removal)
[Deformed slurry 1] was put into a container equipped with a stirrer and a thermometer, and after removing the solvent at 30 ° C for 8 hours, aging was performed at 45 ° C for 4 hours to obtain [Dispersed slurry 1].

(Washing, drying)
[Dispersion Slurry 1] After filtering 100 parts under reduced pressure,
(I) 100 parts of ion-exchanged water was added to the filter cake and mixed with a TK homomixer (rotation speed: 12,000 rpm for 10 minutes) and then filtered.
(Ii) 100 parts of a 10% aqueous sodium hydroxide solution was added to the filter cake of (i), ultrasonic vibration was applied, and the mixture was mixed with a TK homomixer (30 minutes at 12,000 rpm) and then filtered under reduced pressure. This ultrasonic alkali cleaning was performed again (two ultrasonic alkali cleanings).
(Iii) 100 parts of 10% hydrochloric acid was added to the filter cake of (ii), mixed with a TK homomixer (10 minutes at 12,000 rpm), and then filtered.
(Iv) 300 parts of ion-exchanged water was added to the filter cake of (iii), mixed with a TK homomixer (10 minutes at 12,000 rpm), and then filtered twice to obtain [Filter cake 1]. . [Filtration cake 1] was dried at 45 ° C. for 48 hours with a circulating drier, and sieved with a mesh having an opening of 75 μm, whereby toner base 1 was obtained.

<Examples 1-6, Comparative Examples 1-8>
In the above toner manufacturing method, various conditions in the deforming and solvent removal processes were changed to vary the degree of toner shape deforming to some level, and the toner was manufactured. Specifically, conditions such as mixing ratio of ion-exchanged water, activator, and thickener during the profile modification process, rotation speed of TK homomixer, time for solvent removal during the solvent removal process, solvent removal method By sequentially changing detailed conditions and the like, toners having different shape factors SF-1 were obtained. Table 1 shows the physical properties of the obtained toner.

Table 1 also shows the results of image evaluation using the toner. The evaluation items are as follows.
(Evaluation item)
(1) Fixing property Using a RICOH Co., Ltd. imagio NEO 450, a solid image and a thick paper transfer paper (Ricoh type 6200 and NBS RICOH copy printing paper <135>) are solid images of 1.0. Adjustment is made so that toner of ± 0.1 mg / cm ² is developed, and adjustment is made so that the temperature of the fixing belt is variable. Was measured. The lower limit fixing temperature was determined as the fixing lower limit temperature at the fixing roll temperature at which the residual ratio of the image density after rubbing the obtained fixed image with a pad was 70% or more. A fixing lower limit temperature of 170 ° C. or lower was indicated as “◯”, a fixing lower temperature exceeding 170 ° C. and lower than 180 ° C. was indicated as “Δ”, and a fixing lower temperature of 180 ° C. or higher was indicated as “X”.
(2) Cleanability A copying test was conducted using an imagio NEO450, a Ricoh copier. Transfer the residual toner on the photoconductor that has passed through the cleaning process to a white paper with a scotch tape (manufactured by Sumitomo 3M Limited), and measure it with a Macbeth reflection densitometer RD514 type. : The number of sheets where 0.2 or more occurred was evaluated. “◯” indicates the occurrence of 100,000 or more sheets, “Δ” indicates that the occurrence of 75,000 or more and less than 100,000 sheets, and “X” indicates the occurrence of less than 75,000 sheets.
(3) Image quality Image quality was determined comprehensively from transfer failure and image quality degradation (specifically, generation of a soiled image). As for the transfer failure, 50,000 sheets were passed through an imagio NEO450 manufactured by Ricoh Co., Ltd., and then a solid black image was passed through to visually determine the transfer failure level of the image.
Also, for background stain images, 50,000 sheets are passed through the RICOH Co., Ltd. imagio NEO450, then the blank image is stopped during development, and the developer on the photoconductor after development is taped. The difference between the image density of the transferred and untransferred tape was measured by a spectrodensitometer (manufactured by X-Rite) and quantitatively evaluated. Those with good image quality are indicated by “◯”, and those with poor image quality are indicated by “X”.

From Table 1, the toner has a weight average particle size of 3.0 to 6.0 μm, the toner has a shape factor SF-1: A, and a fine powder content ratio B (number%) of 3 μm or less is (Formula 1),
(Formula 1) When 155 ≦ A ≦ 180, 8 ≦ B ≦ 14
When 145 <A <155, 8 ≦ B ≦ 0.6 A−79
In Examples 1 to 6 that satisfy the above conditions, the fixing property, the cleaning property, and the image quality were excellent. On the other hand, Comparative Examples 1 to 8 were out of the above range, and any of the fixing properties, cleaning properties, and image quality was inferior.

It is a figure which shows the flow curve of a flow tester. 1 is a diagram illustrating a schematic configuration of a fixing device according to the present invention. 1 is a diagram illustrating a schematic configuration of an image forming apparatus according to the present invention. It is a figure which shows the structure of an amorphous silicon photoconductor. It is a figure which shows schematic structure of the process cartridge which concerns on this invention.

Explanation of symbols

1 Photosensitive drum (image carrier)
2 Charging roller 3 Exposure device 4 Developing device 6 Transfer belt 7 Fixing device 71 Fixing roller 72 Pressure roller 8 Cleaning blade 500 Amorphous silicon photoconductor 100 Process cartridge 101 Photoconductor 102 Charging means 103 Developing means 104 Cleaning means

Claims (24)

A step of forming a toner image by attaching toner to an electrostatic charge image formed on an image carrier, a step of transferring the toner image onto a recording medium, and a step between two fixing members disposed opposite to each other. Passing the recording medium and fixing the toner image on the recording medium; and cleaning the untransferred toner remaining on the image carrier after the toner image is transferred by a cleaning member in contact with the image carrier. An electrostatic charge image developing toner used in an image forming method comprising:
The toner comprises at least a binder resin, a colorant, and a release agent. The toner has a weight average particle size of 3.0 to 6.0 μm, the toner has a shape factor SF-1: A, and a fine powder content of 3 μm or less. : B (number%) satisfies the following formula 1. An electrostatic charge image developing toner.
(Formula 1) When 155 ≦ A ≦ 180, 8 ≦ B ≦ 14
When 145 <A <155, 8 ≦ B ≦ 0.6 A−79   2. The electrostatic charge image developing toner according to claim 1, wherein the electrostatic charge image developing toner has an outflow start temperature of 90 to 110 [deg.] C. as measured by an elevated flow tester. 3. The fixing step of the image forming method is performed by setting a surface pressure (roller load / contact area) applied between the two fixing members to 1.5 × 10 ⁵ Pa or less. The toner for developing an electrostatic charge image according to 1.   4. The electrostatic charge image according to claim 1, wherein in the cleaning step of the image forming method, cleaning is performed with an elastic rubber blade that is in contact with the rotation direction of the image carrier in a counter direction. Development toner.   The toner for developing an electrostatic image is obtained by dissolving or dispersing a toner composition containing a toner binder component composed of a modified polyester resin (i) capable of reacting with active hydrogen in an organic solvent. It is obtained by reacting with a crosslinking agent and / or an extender in an aqueous medium containing fine particles, removing the solvent from the obtained dispersion, and washing and desorbing the resin fine particles adhering to the toner surface. The toner for developing an electrostatic charge image according to any one of claims 1 to 4.   6. The electrostatic image developing toner according to claim 1, wherein the modified polyester resin (i) is a modified polyester resin having a urea group.   The toner binder component contains an unmodified polyester resin (LL) together with the modified polyester resin (i), and the weight ratio ((i) / (LL)) of (i) to (LL) is 5/95 to The electrostatic image developing toner according to claim 1, wherein the toner is 80/20.   The electrostatic image developing toner according to claim 7, wherein the unmodified polyester resin (LL) has a peak molecular weight of 1,000 to 20,000.   9. The electrostatic image developing toner according to claim 7, wherein the acid value of the unmodified polyester resin (LL) is 10 to 30 mg KOH / g.   The toner for developing an electrostatic charge image according to any one of claims 7 to 8, wherein the glass transition point (Tg) of the unmodified polyester resin (LL) is 35 to 55 ° C.   2. The electrostatic charge image developing toner further comprises a wax, wherein the wax is finely dispersed in the toner and is present in a greater amount in the vicinity of the surface than in the central portion. The toner for developing an electrostatic charge image according to any one of 10.   12. The electrostatic image developing toner according to claim 1, wherein the electrostatic image developing toner has a charge control substance fixed on the surface of toner base particles.   The toner for developing an electrostatic image is obtained by volume shrinkage of a shrinkage of 10 to 90% in an aqueous medium using a solid fine particle dispersant. Toner for developing electrostatic images.   The electrostatic charge image developing toner removes an organic solvent contained therein from a dispersion in which at least fine droplet particles containing an organic solvent, a binder resin, and a colorant are dispersed in an aqueous medium containing resin fine particles. The electrostatic image developing toner according to claim 1, wherein the electrostatic image developing toner is obtained.   A toner container filled with the electrostatic image developing toner according to claim 1.   A developer comprising the electrostatic image developing toner according to claim 1.   A developing device loaded with the developer according to claim 16.   An image forming method comprising developing an electrostatic charge image formed on an image carrier using the developer according to claim 16. An image carrier, an electrostatic image forming unit for forming an electrostatic image on the image carrier, a developing unit for developing the electrostatic image formed on the image carrier with a developer containing toner, and an image carrier A transfer means for transferring the toner image onto the recording medium, a fixing means for fixing the toner image on the recording medium by passing the recording medium between two fixing members arranged opposite to each other, and after the toner image transfer An image forming apparatus comprising: a cleaning unit that cleans untransferred toner remaining on the image carrier with a cleaning member that contacts the image carrier;
An image forming apparatus, wherein the developing unit is loaded with the developer according to claim 16.   The image forming apparatus according to claim 19, wherein the image carrier is an amorphous silicon photoconductor.   21. The image forming apparatus according to claim 19, wherein the developing unit applies an alternating electric field when developing the electrostatic image on the image carrier.   The fixing unit includes a heating body including a heating element, a film in contact with the heating body, and a pressure member in pressure contact with the heating body through the film, and the film and the pressure member The image forming apparatus according to claim 19, wherein the image forming apparatus heats and fixes a recording medium having a toner image transferred therebetween.   23. The image forming apparatus according to claim 19, wherein the charging unit performs charging by bringing a charging member into contact with the image carrier and applying a voltage to the charging member. In a process cartridge that is integrally supported including at least an image carrier and a developing unit, and is detachably formed on the image forming apparatus main body.
17. A process cartridge, wherein the developing means is loaded with the developer according to claim 16.

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