JP2789254B2 - Resin composition for toner and toner for developing electrostatic images using the same - Google Patents

Description

DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a toner resin composition for use in a toner for electrostatic charge development used in electrophotography, electrostatic printing, and magnetic recording, and to a resin composition comprising the same. The present invention relates to a toner for developing an electrostatic image used, particularly a toner suitable for a hot roll fixing method.

[Prior Art] Conventionally, many electrophotographic methods are known as described in U.S. Pat. No. 2,297,691, Japanese Patent Publication No. 42-23910, and Japanese Patent Publication No. 43-24748. However, generally, using a photoconductive substance, an electric latent image is formed on the photoreceptor by various means, and then the latent image is developed using toner, and if necessary, transferred to a transfer material such as paper. After transferring the toner image, the toner image is fixed by heating, pressure, solvent vapor, or the like to obtain a copy.

Various methods and apparatuses have been developed for fixing the toner image to a sheet such as paper, which is the above-mentioned final step, but the most common method at present is a pressure heating method using a heat roller.

In the pressure heating method using a heating roller, fixing is performed by allowing the toner image surface of the sheet to be fixed to pass through the surface of a heat roller having a surface formed of a material having a releasing property with respect to the toner while contacting the surface under pressure. . In this method, since the surface of the heat roller and the toner image of the sheet to be fixed come into contact with each other under pressure, the thermal efficiency at the time of fusing the toner image under the sheet to be fixed is extremely good, and the fixing can be performed quickly. And is very effective in high speed electrophotographic copiers. However, in the above method, since the surface of the heat roller and the toner image come into contact with each other under pressure in a molten state, a part of the toner image adheres / transfers to the surface of the fixing roller, and re-transfers to the next sheet to be fixed. Causing an offset phenomenon,
The sheet to be fixed may be stained. Preventing toner from adhering to the surface of the heat fixing roller is one of the essential conditions of the heat roller fixing method.

Conventionally, for the purpose of preventing the toner from adhering to the surface of the fixing roller, for example, the roller surface is formed of a material having excellent releasability from the toner, such as silicon rubber or a fluorine-based resin, and the surface thereof is further prevented from being offset and the roller is formed. In order to prevent surface fatigue, the roller surface is coated with a thin film of a liquid having good releasability such as silicone oil. However, this method is extremely effective in preventing toner offset, but has a problem that a fixing device is complicated because a device for supplying an anti-offset liquid is required. .

Therefore, it is not preferable that the offset is prevented by supplying the offset preventing liquid. Rather, it is desired to develop a toner having a wide fixing temperature range and a high offset resistance. Therefore, a method of adding a wax such as low-molecular-weight polyethylene or polypropylene that sufficiently melts when heated to increase the releasability as a toner is also performed, but while it is effective in preventing offset,
The cohesiveness of the toner increases, the charging characteristics become unstable, and the durability tends to decrease. Therefore, various attempts have been made to improve the binder resin as another method.

For example, a method is known in which the glass transition temperature (Tg) and the molecular weight of the binder resin in the toner are increased to improve the melt viscoelasticity of the toner. However, such a method has a problem that, when the offset phenomenon is improved, the fixing property becomes insufficient, and the fixing property at a low temperature, that is, the low-temperature fixing property required for high-speed development and energy saving is deteriorated.

In general, in order to improve the low-temperature fixability of a toner, it is necessary to reduce the viscosity of the toner at the time of melting and increase the adhesion area with a fixing base material, and thus lower the Tg and molecular weight of the binder resin used for this purpose. Is required.

That is, since the low-temperature fixing property and the anti-offset property have contradictory aspects, it is very difficult to develop a toner that simultaneously satisfies these functions.

To solve this problem, for example, Japanese Patent Publication No. Sho 51-2335
No. 4, a cross-linking agent and a molecular weight adjusting agent, a toner composed of a moderately cross-linked vinyl polymer,
There are two types of toners, α and β unsaturated ethylenic monomers, whose toner has a wide molecular weight distribution such that the ratio of the weight average molecular weight to the number average molecular weight is 3.5 to 4.0. Regarding coalescence, a large number of blended toners and the like combining Tg, molecular weight, gel content, and the like have been proposed.

Certainly, the toner according to these proposals has a lower fixing temperature (the lowest temperature at which fixing can be performed) and an offset temperature (a temperature at which offset starts to occur), compared to a toner composed of a single resin having a narrow molecular weight distribution. Although the fixing temperature range is widened, if sufficient offset prevention performance is given, the fixing temperature cannot be lowered sufficiently. Conversely, if low-temperature fixing performance is emphasized, the offset prevention performance becomes insufficient. There was.

In place of these vinyl resins, a toner obtained by crosslinking an polyester resin which is considered to be essentially superior to a vinyl resin in terms of low-temperature fixability and further adding an offset preventing agent is also disclosed in -208559. This is excellent in both low-temperature fixability and offset prevention, but has a problem in productivity (pulverizability) as a toner.

In order to improve this, it is disclosed in Japanese Unexamined Patent Publication (Kokai) No. 2002-168370 that a polyester is polymerized in the presence of a low molecular weight polymer containing an acid component.
It is proposed in 61-210367. However, in this case, although the grindability is improved, there are still problems in the blocking resistance and the offset resistance.

As described above, it is extremely difficult to achieve both low-temperature fixing property, offset prevention property and pulverizability related to fixing with high performance. In particular, the pulverizability at the time of toner production is an important factor in today's direction to reduce the particle size of the toner due to the demand for high quality, high resolution and high fine line reproducibility of the copied image. Since the process requires a very large amount of energy, improvement of the pulverizability is important from the viewpoint of energy saving.

Also, the phenomenon of fusion of the toner to the inner wall of the pulverizing device is likely to occur in the toner having good fixing performance, and therefore, the pulverizing efficiency is deteriorated. As another aspect, there is a step of cleaning the toner remaining on the photoconductor after the transfer in another copying step. Today, cleaning with a blade (blade cleaning) has become common in terms of miniaturization, weight reduction, and reliability of the apparatus. As the life of the photoconductor has been prolonged, the size of the photoconductor drum has been reduced, and the speed of the system has been increased, the anti-fusing and filming resistance to the photoconductor required for the toner have become severe. In particular, amorphous silicon photoconductors that have been put into practical use recently have very high durability, and
The life of OPC (organic photoreceptor) has also been extended, and as a result, various properties required for toner have become higher.

In addition, miniaturization requires that each element be placed in a narrow space. As a result, there is less space for air to flow well, and the heat source of the fixing unit and the exposure system is very close to the toner hopper and the cleaner, so that the toner is exposed to a high-temperature atmosphere. Therefore, the toner cannot be put to practical use unless the toner has more excellent blocking resistance.

Furthermore, the various performances required for the above-mentioned toners are often reciprocal to each other, and it is increasingly desired in recent years to satisfy both of them with high performance, and furthermore, the development characteristics are also reduced. Although research has been conducted on comprehensive responses, there is still not enough.

[Problems to be Solved by the Invention] An object of the present invention is to provide a resin composition for a toner as described below and a toner for developing an electrostatic image using the same.

A toner resin composition for use in a toner suitable for a hot roll fixing method without applying oil and a cleaning method using a blade, and a toner for developing an electrostatic image using the same.

A resin composition for a toner which is fixed at a low temperature and is excellent in offset resistance and blocking resistance, and a toner for developing an electrostatic image using the same.

A resin composition for a toner for use in a toner that does not occur in a high-speed system or for a long period of time even when fused and filmed to a photoreceptor and can be sufficiently used in a high-temperature atmosphere in a small machine. Toner for developing electrostatic images.

A toner resin composition for use in a toner with high production efficiency because the pulverized material does not fuse to the inner wall of the device in the pulverization step during toner production and has excellent pulverizability, and an electrostatic charge image using the same Development toner.

A resin composition for a toner for use in a toner that can form a stable and good developed image, and has a small amount of coarse powder and the like due to good pulverizability, so that there is little scattering around the image, and an electrostatic charge image using the same. Development toner.

[Means and Actions for Solving the Problems] The present invention has a THF insoluble content of 5%, which is synthesized by polymerization using one or more vinyl monomers.
% By weight, and in the molecular weight distribution of the THF-soluble component by GPC, a vinyl resin (A) having at least one peak in a molecular weight region of 2,000 to 15,000, and a polybasic acid component and a polyhydric alcohol component as monomers. Number average molecular weight of 1,500 to 10,000, synthesized by condensation polymerization using
Polymerization with a plurality of vinyl monomers and 0.01 to 5% by weight (based on the total weight of all other monomers) in the presence of a polyester resin (C) having 0 and a weight average molecular weight of 6,000 to 200,000. A resin composition synthesized by the method, wherein at the time of synthesizing the resin composition, the amount (A) of the vinyl resin (A) and the amount (B) of the plurality of vinyl monomers used; The weight ratio of the polyester resin (C) to the abundance (C) is as follows: (A) :( B) :( C) = (10-35) :( 20-80):
(5 to 40), and the resin composition contains 5 to 50% by weight (based on the weight of the resin composition) of a THF-insoluble component. The present invention relates to a resin composition for a toner, which has at least one peak in a region of up to 20,000.

Further, the present invention provides a toner for developing an electrostatic image containing at least a binder resin and a colorant, wherein the binder resin is synthesized by polymerizing using one or more vinyl-based monomers. A vinyl-based resin (A) having a content of less than 5% by weight and having at least one peak in a molecular weight region of 2,000 to 15,000 in the molecular weight distribution of THF-soluble components by GPC; A number average molecular weight of 1, synthesized by polycondensation using a polyhydric alcohol component.
Using a plurality of vinyl monomers and 0.01 to 5% by weight (based on the total weight of all other monomers) of a crosslinkable monomer in the presence of a polyester resin (C) having a molecular weight of 500 to 10,000 and a weight average molecular weight of 6,000 to 200,000. A resin composition synthesized by polymerization, wherein at the time of synthesizing the resin composition, the amount (A) of the vinyl resin (A) and the amount (B) of the plurality of vinyl monomers used; The weight ratio of the polyester resin (C) to the abundance (C) is as follows: (A) :( B) :( C) = (10-35) :( 20-80):
(5 to 40), and the resin composition contains 5 to 50% by weight (based on the weight of the resin composition) of a THF-insoluble component. The present invention relates to a toner for developing an electrostatic image, wherein the toner has at least one peak in an area of 20,00020,000.

Here, the THF-insoluble component in the present invention refers to THF in the resin composition.
It indicates the weight ratio of the polymer component (substantially cross-linked polymer) which became insoluble with respect to, and can be used as a parameter indicating the degree of cross-linking of the resin composition containing the cross-linking component. The THF-insoluble matter is defined by a value measured as follows.

That is, 0.5 g of a resin sample (24 mesh pass, 60 mesh on powder) is weighed ( ₁ g of W), put into a cylindrical filter paper (for example, No.86R made by Toyo Filter Paper, size 28 × 100 mm), and put into a Soxhlet extractor. Then, extraction is performed for 12 hours using 150 to 200 ml of THF as a solvent, and the thimble is taken out (one effluent cycle of THF / 4 minutes), dried sufficiently, and the insoluble matter in THF is weighed (W ₂ g). The THF-insoluble content of the resin is obtained from the following equation.

Further, THF residue refers to THF among the resin components in the toner.
Indicates the weight ratio of the hardly extracted or insoluble polymer component (substantially ultrahigh molecular weight polymer), and can be used as a parameter indicating the degree of the presence of the ultrahigh molecular weight component. The THF residue is defined as a value measured as follows.

That is, about 0.5 g of a toner sample is weighed, placed in a cylindrical filter paper (for example, No.86R size 28 × 100 mm manufactured by Toyo Roshi Kaisha, Ltd.), passed through a Soxhlet extractor, and used as a solvent.
Extraction for 12 hours using (THF outflow cycle 1/4
Minutes) Take out the thimble filter paper, dry thoroughly, and weigh the THF residue. The THF residue is calculated by subtracting the pigment and magnetic material weights from the sample toner weight for the non-magnetic toner and the pigment and magnetic material weight (W ₃ g) for the magnetic toner, and the THF residue weight in the toner. Can be calculated from the weight (W ₄ g) obtained by subtracting the weight of the pigment and the magnetic material from the following equation.

In the present invention, the molecular weight of a peak or / and a shoulder of a chromatogram by GPC (gel permeation chromatography) is measured under the following conditions.

 A sample is prepared as follows.

Put the sample in THF, leave it for about 12 hours, shake well, mix well with THF, and let it stand still for more than 12 hours. After that, a sample that has passed through a sample processing filter (pore size: 0.45 μm, for example, Excidox 25CR manufactured by Germanic Science Japan) can be used as a GPC sample.

The sample concentration is adjusted so that the resin component is 0.5 to 5 mg / ml.

In the present invention, the molecular weight of the peak or / and the shoulder of the chromatogram obtained by GPC (gel permeation chromatography) of the THF-soluble component is measured under the following conditions.

That is, the column was stabilized in a heat chamber at 40 ° C, and THF was added to the column at this temperature as a solvent.
(Tetrahydrofuran) is flowed at a flow rate of 1 ml per minute, and about 100 μl of a THF sample solution is injected to measure. In measuring the molecular weight of the sample, the molecular weight distribution of the sample was calculated from the relationship between the logarithmic value of a calibration curve prepared from several types of monodisperse polystyrene standard samples and the count number. As a standard polystyrene sample for preparing a calibration curve, for example, Pressure C
Chemical Co. or Toyo Soda Kogyo Co., Ltd. and Showa Denko KK having a molecular weight of about 10 ² to 10 ⁸ , and it is appropriate to use at least about 10 standard polystyrene samples. An RI (refractive index) detector is used as the detector.

In order to measure the molecular weight region of 10 ² ~3 × 10 ⁷ as the column, often combine several commercially available polystyrene gel column, e.g. Showa Denko Co. shodex G
PC KF-801, 802, 803, 804, 805, 806, 800p combination and Waters Ultra Tyragel 500A-THF, 10
Combinations of ³ A-THF, 10 ⁴ A-THF, 10 ⁵ A-THF, 10 ^-6 A-THF or combinations of the A-Toluene series can be mentioned.

In order to further measure the molecular weight region of 10 ^{2 to} 2 × 10 ⁸ , Shod
ex GPC KF-801,802,803,804,805,806,807,800P.

 The present invention will be described in detail below.

In order to simultaneously achieve the above objects, various binder resins were used, and the structure and performance of the resin were studied from various angles. As a result, it has been found that the ratio of the THF-insoluble component of the binder resin and the molecular weight distribution of the THF-soluble component can be achieved when the specific configuration is achieved. TH binder resin
When dissolved in a solvent such as F, it can be separated into an insoluble matter and a soluble matter, and the molecular weight distribution of the soluble matter can be measured by GPC. Focusing on the positions of the peaks of the molecular weight distributions of THF-insoluble matter and THF-soluble matter, a system having no or little THF-insoluble matter is very disadvantageous in pulverizability, and as described above, THF is used to improve pulverizability. The direction in which the position of the peak of the molecular weight distribution of the dissolved component is simply shifted to the position of a low molecular weight deteriorates the offset resistance, which supports that it is difficult to satisfy both the offset resistance and the pulverizability.

From this study, it has been found that it is very effective to include a specific amount of THF-insoluble matter not only for offset resistance but also for improving pulverizability, as generally considered.

Furthermore, the molecular weight distribution of the THF-soluble component and the property of whether the fixable temperature is high or low (hereinafter simply referred to as fixability), offset resistance, crushability, and blocking resistance were examined. As a result, it has been found that the functions of components having a molecular weight of about 10,000 or less and about 10,000 or more in the GPC molecular weight distribution are different. That is, the content ratio of the component having a molecular weight of 10,000 or less with respect to the whole binder resin does not strongly influence the fixing property or the anti-offset property, as is generally said, but is almost related to either in a specific range. Instead, it was found to be strongly related to the crushability.

Furthermore, from other investigations, etc., in the binder resin, the THF-insoluble component basically affects the offset resistance, winding property, and crushability, and the THF-soluble component having a molecular weight of 10,000 or less is mainly crushable. Influences the blocking property, the fusion property to the photoreceptor, the filming property and the fusion to the inner wall of the pulverizer, and the THF-soluble component having a molecular weight of 10,000 or more affects the offset resistance and the fixing property. Among various binder resins, it has been found that a polyester resin comprising a condensate of a polybasic acid component and a polyhydric alcohol component exhibits the best fixing property.

For this reason, the polyester resin has a lower critical surface tension than that of paper, and furthermore, an ester group which is a main polar group and a carboxyl group and a hydroxyl group coexisting in the molecule have an affinity for a hydroxyl group of the paper with a hydrogen bond, This is because it is considered that the fixing effect is improved.

More specifically, the resin composition for toner used as a binder resin in the toner of the present invention has a THF insoluble content (gel content) of 5 to 50% by weight (based on the binder resin), preferably 10 to 50% by weight. Contains 45% by weight.
The reason for this is that when the THF-insoluble content in the resin composition exceeds 50% by weight, when used in a toner,
This leads to an increase in the fixing temperature, and further the dispersion of the additive becomes worse.
Further, the components of the highly crosslinked region are liable to be cut off during the kneading of the resin, which may hinder the design of the toner. Conversely, the gel content is 5
If the content is less than 5% by weight, offset and winding around a roller are apt to occur. If the gel content is less than 5% by weight and the high molecular weight region is large, the pulverizability is remarkably deteriorated.

The resin composition for a toner of the present invention is obtained by condensing a vinyl resin (A) synthesized by polymerization using one or more vinyl monomers and a polybasic acid component and a polyhydric alcohol component as monomers. It is synthesized by polymerization using a plurality of vinyl monomers and a crosslinkable monomer in the presence of the polyester resin (C) synthesized by polymerization.

The vinyl resin (A) has a THF-insoluble content of
The content is preferably less than 5% by weight, preferably less than 3% by weight.
2,000 to 15,000 region, preferably molecular weight 2,000 to 12,000
It is good to have at least one peak in the region.

The polyester resin (C) has a number average molecular weight of 1,500
It preferably has a weight average molecular weight of 6,000 to 200,000.

When synthesizing the resin composition for toner by the above method,
The weight ratio of the amount (A) of the vinyl resin (A), the amount (B) of the plurality of vinyl monomers used, and the amount (C) of the polyester resin (C) has the following relationship (A): (B): (C) = (10-35): (20-80):
(5 to 40) is preferably satisfied, and preferably the following relationship (A): (B): (C) = (10 to 35): (25 to 75):
(5-35) should be satisfied.

The reason for the compounding ratio of each component is that when the ratio (A) of the vinyl [resin] (A) exceeds 35, the offset resistance and the blocking resistance are insufficient.
If less than, as is apparent from Comparative Example 1 described below,
The pulverizability during toner production decreases. If the ratio (B) of the plurality of vinyl monomers is less than 20, the offset or blocking is adversely affected, and if the ratio is more than 80, the pulverizability is poor, and the production is adversely affected such as generation of coarse powder. Further, when the proportion (C) of the polyester resin (C) is less than 5, the effect of the addition of the polyester resin is not sufficiently exhibited, and the fixability or developability is poor. Poor performance causes problems in production.

Examples of the comonomer for obtaining the vinyl copolymer which is a part of the constituent components of the binder resin of the present invention include the following.

For example, styrene, o-methylstyrene, m-methylstyrene, p-methylstyrene, p-methoxystyrene,
p-phenylstyrene, p-chlorostyrene, 3,4-dichlorostyrene, p-ethylstyrene, 2,4-dimethylstyrene, pn-butylstyrene, p-tert-butylstyrene, pn-hexylstyrene Styrene and its derivatives such as pn-octylstyrene, pn-nonylstyrene, pn-decylstyrene and pn-dodecylstyrene; ethylenically unsaturated monoolefins such as ethylene, propylene, butylene and isobutylene Unsaturated vinylenes such as butadiene; vinyl halides such as vinyl chloride, vinylidene chloride, vinyl bromide, and vinyl fluoride; vinyl esters such as vinyl acetate, vinyl propionate and vinyl benzoate; methyl methacrylate; Ethyl methacrylate, propyl methacrylate, n-butyl methacrylate, methacryl Isobutyl acid, methacrylic acid n
-Octyl, dodecyl methacrylate, methacrylic acid-2
Α-methylene aliphatic monocarboxylic esters such as ethylhexyl, stearyl methacrylate, phenyl methacrylate, dimethylaminoethyl methacrylate and diethylaminoethyl methacrylate; methyl acrylate, ethyl acrylate, n-butyl acrylate, acrylic acid Acrylic esters such as isobutyl, propyl acrylate, n-octyl acrylate, dodecyl acrylate, 2-ethylhexyl acrylate, stearyl acrylate, 2-chloroethyl acrylate and phenyl acrylate;
Vinyl ethers such as vinyl methyl ether, vinyl ethyl ether and vinyl isobutyl ether; vinyl ketones such as vinyl methyl ketone, vinyl hexyl ketone and methyl isopropenyl ketone; N-vinyl pyrrole;
N-vinyl carbazole, N-vinyl indole, N-
Vinyl monomers such as N-vinyl compounds such as vinyl pyrrolidone; vinyl naphthalenes; acrylic acid or methacrylic acid derivatives such as acrylonitrile, methacrylonitrile, and acrylamide; are used alone or in combination of two or more.

Among these, a combination of monomers that results in a styrene-based copolymer and a styrene-acrylic copolymer is preferred.

As the crosslinkable monomer, a monomer having two or more polymerizable double bonds is mainly used.

The vinyl copolymer used in the present invention needs to be a polymer cross-linked with a cross-linkable monomer as exemplified below in order to achieve the object of the present invention.

Aromatic divinyl compounds, for example, divinylbenzene,
Divinylnaphthalene and the like; diacrylate compounds linked by an alkyl chain, for example, ethylene glycol diacrylate, 1,3-butylene glycol diacrylate, 1,4
-Butanediol diacrylate, 1,5-pentanediol diacrylate, 1,6-hexanediol diacrylate, neopentyl glycol diacrylate, and acrylates of the above compounds replaced with methacrylates; alkyl chains containing ether linkages Diacrylate compounds, such as diethylene glycol diacrylate, triethylene glycol diacrylate, tetraethylene glycol diacrylate, polyethylene glycol # 400 diacrylate, polyethylene glycol # 600 diacrylate, dipropylene glycol diacrylate, and the like Compounds in which acrylate is replaced with methacrylate; diacrylate compounds linked by a chain containing an aromatic group and an ether bond, for example, polyoxyethylene ( ) -2,2-bis (4-hydroxyphenyl) propane diacrylate, polyoxyethylene (4) -2,2-bis (4-hydroxyphenyl) propane diacrylate, and acrylates of the above compounds as methacrylates Replaced; furthermore,
Polyester type diacrylate compounds, for example, trade name MANDA (Nippon Kayaku) are listed. Examples of the multifunctional crosslinking agent include pentaerythritol triacrylate, trimethylolethane triacrylate, trimethylolpropane triacrylate, tetramethylolmethanetetraacrylate, oligoester acrylate, and those obtained by replacing the acrylate of the above compound with methacrylate; Allyl cyanurate, triallyl trimellitate; and the like.

These crosslinkable monomers contain all other monomer components 100
0.01 to 5 parts by weight, preferably 0.03 to 3 parts by weight based on parts by weight
It is preferable to use parts by weight.

Here, 100 parts by weight of all the other monomer components are the vinyl monomer used in synthesizing the vinyl resin (A), the polybasic acid component and the monomer used in synthesizing the polyester resin (C). This means that the total weight of the polyhydric alcohol component and the plurality of vinyl monomers used in the synthesis of the resin composition is 100 parts by weight.

Among these crosslinkable monomers, those which are preferably used in the toner resin from the viewpoint of fixability and anti-offset properties include an aromatic divinyl compound (particularly divinylbenzene), a chain containing an aromatic group and an ether bond. Diacrylate compounds.

Further, the composition of the polyester resin (C) used in the present invention is as follows.

As the dihydric alcohol component, ethylene glycol, propylene glycol, 1,3-butanediol, 1,4
-Butanediol, 2,3-butanediol, diethylene glycol, triethylene glycol, 1,5-pentanediol, 1,6-hexanediol, neopentyl glycol, 2-ethyl-1,3-hexanediol, hydrogenated bisphenol A Or a bisphenol represented by the formula (A) and a derivative thereof; (Where R is an ethylene or propylene group, x and y are each an integer of 0 or more, and the average value of x + y is 0
Diols represented by the formula (B): And diols such as

Examples of the divalent acid component include benzenedicarboxylic acids such as phthalic acid, terephthalic acid, isophthalic acid and phthalic anhydride or anhydrides thereof, lower alkyl esters; succinic acid,
Alkyl dicarboxylic acids such as adipic acid, sebacic acid and azelaic acid or their anhydrides and lower alkyl esters; alkenyl succinic acids and alkyl succinic acids such as n-dodecenyl succinic acid and n-dodecyl succinic acid, or anhydrides and lower alkyl esters thereof And unsaturated dicarboxylic acids such as fumaric acid, maleic acid, citraconic acid and itaconic acid or anhydrides thereof, dicarboxylic acids such as lower alkyl esters, and derivatives thereof.

Further, a trivalent or higher valent alcohol component and a trivalent or higher valent acid component which also serve as a crosslinking component can be used in combination.

The trihydric or higher polyhydric alcohol component in the present invention includes sorbitol, 1,2,3,6-hexanetetrol, 1,4
-Sorbitan, pentaerythritol, dipentaerythritol, tripentaerythritol, 1,2,4-butanetriol, 1,2,5-pentanetriol, glycerol, 2-methylpropanetriol, 2-methyl-1,2,
4-butanetriol, trimethylolethane, trimethylolpropane, 1,3,5-trihydroxybenzene,
And the like.

In the present invention, the trivalent or higher polyvalent carboxylic acid component includes trimellitic acid, pyromellitic acid, 1,2,4-benzenetricarboxylic acid, 1,2,5-benzenetricarboxylic acid, 2,5,7 -Naphthalenetricarboxylic acid, 1,2,4-naphthalenetricarboxylic acid, 1,2,4-butanetricarboxylic acid,
1,2,5-hexanetricarboxylic acid, 1,3-dicarboxyl-2-methyl-2-methylenecarboxypropane, tetra (methylenecarboxyl) methane, 1,2,7,8-octanetetracarboxylic acid, embol trimer Body acids and their anhydrides, lower alkyl esters, (Wherein X is an alkylene group or alkenylene group having 5 to 30 carbon atoms having at least one side chain having 3 or more carbon atoms), and polyhydric compounds such as anhydrides and lower alkyl esters thereof. Examples include carboxylic acids and derivatives thereof.

35-65mo as the alcohol component used in the present invention
l%, preferably 40-60 mol%, 65-35mo as acid component
l%, preferably 60 to 40 mol%.

The trivalent or higher polyvalent component accounts for 5 to 60 mol of all components.
% Is desirable.

In the present invention, the alcohol component of the polyester resin (C) is preferably a bisphenol derivative represented by the formula (A), and the acid component is phthalic acid, terephthalic acid, isophthalic acid or anhydride thereof; succinic acid ,
n-dodecenyl succinic acid or its anhydride; dicarboxylic acids such as fumaric acid, maleic acid, and maleic anhydride; and trimellitic acid or its tricarboxylic acid anhydride, and the like.

This is because the polyester resin obtained with these acids and alcohols exhibits sharp melting characteristics, has good fixing properties as a heat roller fixing toner, and has excellent offset resistance.

The polyether resin (C) used in the present invention has a number average molecular weight of 1,500 to 10,000, preferably 2,000 to 7,000 and a weight average molecular weight of 6,000 to 200,000, preferably 10,000 to 15,
The glass transition temperature is preferably 50 to 70 ° C, more preferably 55 to 65 ° C.
It is good to be ° C.

It is desirable that the acid value is 100 or less, preferably 50 or less, and the hydroxyl value is 60 or less, preferably 30 or less. This is because when the number of terminal groups in the molecular chain increases, the toner becomes
This is because the charging characteristics of the toner are greatly dependent on the environment.

Here, the acid value and the hydroxyl value of the resin were measured by the following methods.

2 to 10 g of a sample are weighed in a 200 to 300 ml Erlenmeyer flask, and about 50 ml of a mixed solvent of methanol: toluene = 30: 70 is added to dissolve the resin. If the solubility is poor, a small amount of acetone may be added. Using a mixed indicator of 0.1% bromthymol blue and phenol red, titrate with a pre-specified N / 10 potassium hydroxide-alcohol solution. I asked.

Acid value = KOH (ml) × N × 56.1 / Sample weight (3) (where N is a factor of N / 10 KOH) The hydroxyl value is determined by heating the sample with an excess acetylating agent such as acetic anhydride. After the acetylation is performed and the saponification value of the acetylated product is measured, it is calculated according to the following equation (4).

(However, A represents the saponification value after acetylation, and B represents the saponification value before acetylation.) The method for synthesizing the binder resin according to the present invention is basically a method for synthesizing two or more polymers. preferable.

That is, a first polymer (vinyl-based [resin] (A)) and a polyester resin (C), which are low in THF and are soluble in the polymerizable monomer, are dissolved in the polymerizable monomer, and the monomer is polymerized to form a resin composition. It is a way to get things. In this case, a composition is formed in which the former and the latter polymers are uniformly mixed.

The low molecular weight polymer (vinyl [resin] (A)) in the binder resin composition used in the present invention can be obtained by a commonly used polymerization method such as a bulk polymerization method and a solution polymerization method.

In the bulk polymerization method, by polymerizing at a high temperature to increase the termination reaction rate, a low molecular weight polymer can be obtained.
There is a problem that it is difficult to control the reaction. In this regard, in the solution polymerization method, a low molecular weight polymer can be easily obtained under mild conditions by utilizing the difference in radical chain transfer depending on the solvent, and by adjusting the amount of the initiator and the reaction temperature. It is preferable to obtain a low molecular weight polymer in the resin composition used in the above.

As the solvent used in the solution polymerization, xylene, toluene, cumene, cellosolve acetate, isopropyl alcohol, benzene and the like are used. In the case of a testyrene monomer, xylene, toluene or cumene is preferred. It is appropriately selected depending on the polymer to be polymerized. The initiator is
Di-tert-butyl peroxide, tert-butyl peroxybenzoate, benzoyl peroxide, 2,2'-
Azobisisobutyronitrile, 2,2'-azobis (2,4 dimethylvaleronitrile) and the like are used in a concentration of 0.1 part by weight or more (preferably 0.4 to 15 parts by weight) based on 100 parts by weight of the monomer. The reaction temperature varies depending on the solvent used, the initiator, and the polymer to be polymerized.
It is good to do in. In the solution polymerization, the polymerization is preferably carried out at 30 to 400 parts by weight of the monomer with respect to 100 parts by weight of the solvent.

This low molecular weight polymer is polymerized again together with the polyester resin and the monomer giving the medium / high molecular weight polymer, but as a polymerization method for obtaining a crosslinked region or a gel component until it becomes an insoluble component in a solvent, an emulsion polymerization method is used. Preference is given to a synthetic method or a suspension polymerization method.

Among them, the emulsion polymerization method is a method in which a monomer (monomer) almost insoluble in water is dispersed as small particles in an aqueous phase with an emulsifier, and polymerization is carried out using a water-soluble polymerization initiator. In this method, it is easy to control the heat of reaction, and since the phase in which the polymerization is performed (the oil phase composed of the polymer and the monomer) and the aqueous phase are separate, the termination reaction rate is small, and as a result, the polymerization rate is low. Large and high degree of polymerization can be obtained. Furthermore, the polymerization process is relatively simple, and the polymerization product is fine particles, so that it is easy to mix with a colorant, a charge control agent, and other additives in the production of a toner. This is advantageous as compared with other methods as a method for producing a binder resin for a toner.

However, the resulting polymer tends to be impure due to the added emulsifier, and an operation such as salting out is required to take out the polymer. To avoid this inconvenience, suspension polymerization is advantageous.

Taking the suspension polymerization method as an example, the monomer containing the low-molecular-weight polymer in suspension is polymerized together with the crosslinking agent, so that the resin composition is shaped like a pearl and the low-molecular-weight polymer is formed. To the high-molecular-weight polymer containing the components of the cross-linking region to the high-molecular-weight polymer in a preferable state uniformly mixed.

In the suspension polymerization, based on 100 parts by weight of the aqueous solvent,
It is better to use the polyester resin and the monomer at 100 parts by weight or less (preferably 10 to 90 parts by weight). As a dispersant that can be used, polyvinyl alcohol, partially saponified polyvinyl alcohol, calcium phosphate and the like are used, and the amount is an appropriate amount in terms of the amount of a monomer with respect to an aqueous solvent, but is generally 0.05 to 1 part by weight based on 100 parts by weight of an aqueous solvent. Used in
The polymerization temperature is suitably 50 to 95 ° C, but the initiator used,
It should be appropriately selected depending on the desired polymer. As the initiator type, any one can be used as long as it is insoluble or hardly soluble in water, for example, benzoyl peroxide, tert-butyl peroxyhexanoate, etc.
It is used in an amount of 0.5 to 10 parts by weight based on 100 parts by weight of the monomer.

In the toner of the present invention, a conventionally known negative or positive charge control agent is used.

Today, charge control agents known in the art include:

The following substances control the toner to be negatively charged.

For example, an organic metal complex and a chelate compound are effective, and examples thereof include a monoazo metal complex, an acetylacetone metal complex, an aromatic hydroxycarboxylic acid, and an aromatic dicarboxylic acid-based metal complex. In addition, aromatic hydroxycarboxylic acids, aromatic mono- and polycarboxylic acids and metal salts, anhydrides and esters thereof. Phenol derivatives such as bisphenol.

The following substances control the toner to be positively charged. Modified products such as nigrosine and fatty acid metal salts. Onium salts such as quaternary ammonium salts such as tributylbenzylammonium-1-hydroxy-4-naphthosulfonate and tetrabutylammonium tetrafluoroborate, and analogs thereof such as phosphonium salts and lake pigments thereof. Triphenylmethane dyes and their lake pigments. (As the lake-forming agent, phosphotungstic acid, phosphomolybdic acid, phosphotungsten molybdic acid, tannic acid, lauric acid, gallic acid, ferricyanide, ferrocyanide, etc.) Metal salts of higher fatty acids, acetylacetone metal complexes. Dibutyltin oxide, dioctyltin oxide; diorganotin oxides such as dicyclohexyltin oxide, diorganotin borates such as dibutyltin borate, dioctyltin borate and dicyclohexyltin borate. These can be used alone or in combination of two or more. Among these, charge control agents such as nigrosine and quaternary ammonium salts are particularly preferably used.

The amount of the charge control agent added to the toner particles may vary depending on the type of the toner binder resin, whether or not the carrier is used together, or the pigment for coloring the toner. It is 20% by weight, preferably 0.1 to 10% by weight.

In the toner of the present invention, it is preferable to add fine silica powder in order to improve charging stability, developability, fluidity, and durability.

The silica fine powder used in the present invention has a specific surface area by nitrogen adsorption measured by the BET method of 30 m ² / g or more (particularly 50 to 400 m
² / g) gives good results. Toner 100
It is preferable to use 0.01 to 8 parts by weight, preferably 0.1 to 5 parts by weight of silica fine powder based on parts by weight.

Also, the silica fine powder used in the present invention, if necessary,
Treatment agents such as silicone varnish, various modified silicone varnishes, silicone oil, various modified silicone oils, silane coupling agents, silane coupling agents having functional groups, and other organosilicon compounds for the purpose of hydrophobicity, charge control, etc. Alternatively, it is also preferred that the composition is treated in combination with various treatment agents.

As other additives, for example, lubricants such as Teflon, zinc stearate, and polyvinylidene fluoride are preferable, and polyvinylidene fluoride is particularly preferable. Alternatively, abrasives such as cerium oxide, silicon carbide, and strontium titanate, among which strontium titanate is preferable. Or, for example, titanium oxide,
Fluidity-imparting agents such as aluminum oxide, particularly hydrophobic ones are preferred. A small amount of a caking inhibitor, a conductivity-imparting agent such as carbon black, zinc oxide, antimony oxide, and tin oxide, or white and black fine particles of opposite polarity can also be used as a developability improver.

For the purpose of improving the releasability at the time of fixing with a hot roll, a wax-like substance such as low-molecular-weight polyethylene, low-molecular-weight polypropylene, microcrystalline wax, carnauba wax, sasol wax, paraffin wax, etc. is added in an amount of 0.5 to 100% by weight of the binder resin. Addition of about 10% by weight to the toner is also a preferred embodiment of the present invention.

Further, when used as a two-component developer, the toner of the present invention is used by mixing with a carrier powder. In this case, the mixing ratio of the toner and the carrier powder is defined as the toner concentration.
0.1 to 50% by weight, preferably 0.5 to 10% by weight, more preferably 3 to 5% by weight.

As the carrier that can be used in the present invention, all known carriers can be used, for example, iron powder, ferrite powder, magnetic powder such as nickel powder, glass beads, and the like, and the surface thereof is a fluororesin, vinyl And a resin treated with a silicone resin or a silicone resin.

Further, the toner of the present invention may contain a magnetic material and be used as a magnetic toner. In this case, the magnetic material also serves as a colorant. Examples of the magnetic material contained in the magnetic toner of the present invention include iron oxides such as magnetite, hematite, and ferrite; metals such as iron, cobalt, and nickel; or aluminum, cobalt, copper, lead, magnesium, and tin of these metals. Zinc, antimony, beryllium, bismuth, cadmium, calcium, manganese, selenium,
Examples include alloys of metals such as titanium, tungsten, and vanadium, and mixtures thereof.

These ferromagnetic substances preferably have an average particle size of about 0.1 to 2 μm, preferably about 0.1 to 0.5 μm. The amount of the ferromagnetic substance contained in the toner is preferably about 20 to 200 parts by weight per 100 parts by weight of the resin component.
Parts by weight, particularly preferably 40 to 1 to 100 parts by weight of the resin component.
50 parts by weight is good.

Further, it is desirable that the magnetic properties at 10 Ke applied have a coercive force of 20 to 150 saturation magnetization of 50 to 200 emu / g and a residual magnetization of 2 to 20 emu / g.

Colorants that can be used in the toner of the present invention include any suitable pigments or dyes. Toner colorants are well known and include pigments such as carbon black, aniline black, acetylene black, naphthol yellow, hansa yellow, rhodamine lake, alizarin lake, bengara, phthalocyanine blue, and indanthrene blue. These are used in an amount necessary and sufficient to maintain the optical density of the fixed image, and 0.1 to 20 parts by weight, preferably 2 to 10 parts by weight, per 100 parts by weight of the resin is good. For the same purpose, a dye is further used. For example, there are azo dyes, anthraquinone dyes, xanthene dyes, methine dyes, etc.
An addition amount of 20 parts by weight, preferably 0.3 to 3 parts by weight is good.

To prepare the toner for developing an electrostatic image according to the present invention, a binder resin, a metal compound, a pigment as a coloring agent or a dye, a magnetic substance, a charge control agent, if necessary, and other additives are added to a Henschel mixer. , Kneading and kneading using a hot kneading machine such as a heating roll, kneader, extruder, etc. ,
The toner according to the present invention can be obtained by dispersing or dissolving the dye and the magnetic substance, and solidifying by cooling, followed by pulverization and classification.

Further, if necessary, desired additives are sufficiently mixed by a mixer such as a Henschel mixer to obtain the toner for developing an electrostatic image according to the present invention.

[Examples] Hereinafter, the present invention will be described with reference to specific examples, but the present invention is not limited thereto. Less than,
“Parts” all mean parts by weight.

Synthesis Example 1 The above components were added dropwise over 4 hours to 200 parts of cumene heated to the reflux temperature. Further under cumene reflux (146-156
C), the solution polymerization was completed, and cumene was removed. The obtained copolymer has a molecular weight of 4000, the main peak of GPC is located.
Tg = 60 ° C.

30 parts of the copolymer was dissolved in the following monomer mixture to prepare a mixed solution.

In the above mixed solution, partially saponified polyvinyl alcohol
170 parts of water in which 0.1 part was dissolved was added to obtain a suspension dispersion. water
The above-mentioned suspension dispersion was added to a reactor in which 15 parts had been charged and purged with nitrogen, and after the reaction was completed, dehydrated and dried to obtain a binder resin composition. In the composition, a THF-insoluble component and a THF-soluble component were uniformly mixed, and a vinyl copolymer and a polyester resin were uniformly mixed. THF of the obtained resin composition
The insoluble content was 32% by weight. When the molecular weight distribution of the THF-soluble component was measured, the GPC chart showed that the molecular weight distribution was approximately 1.4%.
It had a peak at the 10,000 position, and the Tg of the resin was 59 ° C. Tg
Was determined by annealing the resin at 50 ° C. for 48 hours, and then by differential scanning calorimetry.

Synthesis Example 2 The above components were added dropwise to 200 parts of xylene heated to the reflux temperature over 4 hours. Furthermore, under xylene reflux (138
〜144 ° C.) to complete the solution polymerization and remove xylene.
The obtained copolymer had a molecular weight at which the main peak of GPC was located at 6000, and Tg = 61 ° C.

10 parts of the copolymer was dissolved in the following monomer mixture to obtain a mixture.

170 parts of water in which 1 part of a partially saponified polyvinyl alcohol was dissolved was added to the above mixture to obtain a suspension dispersion. The above dispersion was added to a reactor which was filled with 15 parts of water and purged with nitrogen, and reacted at a reaction temperature of 70 to 95 ° C. for 6 hours. After completion of the reaction, dehydration and drying were performed separately to obtain a resin composition. The THF insoluble content of the obtained resin composition was 40% by weight. Further, when the molecular weight distribution of the THF-soluble component was measured, it was found that the peak was at about 10,000 and the shoulder was at about 50,000 in the GPC chart. The Tg of the resin was 58.5 ° C.

Synthesis Example 3 150 parts of cumene was put into the reactor, and the temperature was raised to the reflux temperature. Further, the mixture was added dropwise over 4 hours under cumene reflux. Then, the polymerization was completed under cumene reflux (146 to 156 ° C.), and cumene was removed. The obtained polystyrene had a main peak at a molecular weight of 7000, and had a Tg of 72 ° C. 35 parts of the above polystyrene was dissolved in the following monomer mixture to give a mixture.

Polyvinyl alcohol partially saponified 0.1 to the above mixture
170 parts of water in which the above parts were dissolved was added to obtain a suspension dispersion. The above dispersion was added to a reactor which was filled with 15 parts of water and purged with nitrogen, and reacted at a reaction temperature of 70 to 95 ° C. for 6 hours. After the reaction is completed,
Dehydrated and dried, polystyrene and styrene-acrylic acid
-A composition of a copolymer of butyl and polyester was obtained.

In the GPC chart, the obtained resin had a peak at 80,000, a shoulder at 64,000, and a THF-insoluble content of 38% by weight. Tg was 57.5 ° C. and the acid value was 17.0.

Comparative Synthesis Example 1 In the above mixed solution, partially saponified polyvinyl alcohol
170 parts of water in which 0.1 part was dissolved was added to obtain a dispersion. The above dispersion was added to a reactor which was filled with 15 parts of water and purged with nitrogen, and reacted at a reaction temperature of 70 to 95 ° C. for 6 hours. After completion of the reaction, the mixture was separated, dehydrated and dried to obtain a resin composition. The molecular weight distribution of the obtained resin had a peak at 50,000, a shoulder at 60,000, a THF-insoluble content of 45% by weight, and Tg of 59 ° C.

Comparative Synthesis Example 2 In Synthesis Example 1, the low molecular weight type vinyl copolymer (A) obtained in the solution polymerization was changed to 60 parts, styrene monomer 20 parts, n-butyl acrylate 15 parts, and polyester resin 5 parts. A resin composition was obtained by suspension polymerization according to the same formulation as in Synthesis Example 1 except for the above. The obtained resin is THF
In the GPC chart of the soluble component, the peak was at the position of 0.4000, the shoulder was at the position of 10,000, and the THF-insoluble content was 3% by weight. The Tg was 48 ° C.

Comparative Synthesis Example 3 A resin composition was obtained in the same manner as in Synthesis Example 1 except that the polyester resin was not added during the suspension polymerization. The obtained resin has a peak at a position of about 66,000 and about 52,000 in a GPC chart of a THF-soluble component,
The insoluble content was 15% by weight, and the Tg of the resin was 57 ° C.

Comparative Synthesis Example 4 In Synthesis Example 1, the low molecular weight type vinyl copolymer (A) obtained by solution polymerization was changed to 5 parts, styrene monomer 61 parts, n-butyl acrylate 29 parts, and polyester resin 5 parts. A resin composition was obtained by suspension polymerization according to the same formulation as in Synthesis Example 1 except for the above. The obtained resin is THF
In the GPC chart of the soluble matter, there was a peak at about 60,000 and a shoulder at 120,000. The THF insoluble content was 55% by weight. Tg was 60 ° C.

Example 1 After premixing the above ingredients with a Henschel mixer, 130
Melt kneading was performed at 2 ° C. by a twin screw kneading extruder. After allowing the kneaded material to cool, coarsely pulverized by a cutter mill, pulverized using a fine pulverizer using a jet stream, and further classified using an air classifier, the black fine powder having a volume average particle size of 8.5 μm ( Toner). The melt index value of this toner was 5.8 when measured under the conditions of 125 ° C. and 10 kg using an apparatus described in JIS K7210.

With respect to 100 parts of the toner, hydrophobic colloidal silica 0.4
Parts were dry-mixed to obtain a developer.

This developer was evaluated for image properties, fixability, anti-offset property and the like using a Canon copier NP-8580 using an α-Si photoreceptor. The resulting copied image had a high reflection image density of 1.35, had no fog, was free of toner scattering around the image, and had a good image with high resolution. Regarding the durability, the image after copying 200,000 sheets is an image which has no stain in comparison with the initial image, although the fixing roller and the cleaning member (web) have some stains. In addition, there was almost no filming or fusing to the photoreceptor, and the fixing roller was not contaminated by copying.

The anti-blocking property was examined by a change in agglomeration when about 10 g of the toner was put in a 100 cc polycup and allowed to stand at 50 ° C. for one day. The degree of aggregation was measured with a powder tester manufactured by Hosokawa Micron. The sign of blocking resistance is the same as the one left at room temperature.
The difference between the cohesion degrees of the items left at 50 ° C. for one day was determined.

Fixing and offset resistance, winding resistance and image quality,
The durability was evaluated in the following procedure.

The fixability was evaluated by leaving the evaluation machine overnight in a low-temperature and low-humidity environment (15 ° C, 10%). A copy image was taken, and the 200th copy image was used for evaluation of fixability. Evaluation of fixability is about 10 round trips of the image on symbol paper 10 times
Rubbing was carried out with a load of 0 g, and the peeling of the image was evaluated by the reduction rate (%) of the reflection density.

In particular, the anti-offset property was evaluated by removing the cleaning mechanism of the fixing roller and determining the number of copies of the image or the roller to be stained by the anti-copy number.

Also, depending on the state of dirt on the cleaning wave when continuous copying is performed, the toner once taken by the cleaning wave may transfer to the upper roller and contaminate the copy. For this purpose, the cleaning mechanism of the fixing roller was returned to the normal state, and after taking 200 continuous copies, the copies were taken at 30-second intervals, one at a time, up to 3 minutes, to check whether image contamination occurred, and The state of dirt on the cleaning wave of the fixing roller was evaluated.

The anti-winding property indicates the evaluation of the anti-winding property when 30 copies of the entire black image are continuously copied and the copied image that has passed through the fixing roller may be curled in such a way that the curling occurs. Mark.

 The results of the image evaluation are shown in the following table.

Example 2 The above materials were converted to toner by the same method as in Example 1 to obtain a developer. Image evaluation was performed in the same manner as in Example 1. The results are shown in the table below.

Example 3 The above-mentioned materials were converted to toner by the same method as in Example 1, and a developer was obtained. Image evaluation was performed in the same manner as in Example 1. The results are shown in the table below.

Comparative Example 1 A toner was produced and evaluated in the same manner as in Example 1 except that the resin binder obtained in Comparative Synthesis Example 1 was used. The results are shown in the table below.

Example 4 A toner was prepared in the same manner as in Example 1 except that 5 parts of carbon black was added instead of magnetite. To 8 parts of this toner, 100 parts of a ferrite carrier (particle size: about 80 μm) whose surface was coated with a fluororesin was mixed to prepare a developer. As a replenisher, only toner was used. The image of this developer was evaluated by a Canon copier NP-6650, and the image was good. A stable image was obtained although 200,000 sheets were durable. No filming or fusion of the toner on the photosensitive drum was observed.

Example 5 A toner was prepared in the same manner as in Example 1 except that 5 parts of nigrosine was added instead of the monoazo iron complex. For image evaluation, the NP8580 was modified and evaluated with a machine equipped with a reversal developing mechanism. As a result, good images could be obtained. Detailed results are shown in the table.

Comparative Example 2 A toner was manufactured and evaluated in the same manner as in Example 1 except that the resin obtained in Comparative Synthesis Example 2 was used. As shown in the table, the obtained toner was inferior in anti-blocking property and anti-offset property. When the fixing roller was examined after copying 200,000 sheets, it was confirmed that the toner was stained black. Also, during copying, paper jam (jam) frequently occurred due to the fusion of the toner to the fixing / separating claw.

Comparative Example 3 A toner was manufactured and evaluated in the same manner as in Example 1, except that the resin obtained in Comparative Synthesis Example 3 was used. As a result, the image density was 1.25 to 1.30, and the density reduction rate in the fixability test was 20.
%, Which is slightly inferior to the toner manufactured in Example 1.

Comparative Example 4 A toner was produced in the same manner as in Example 1 except that the resin obtained in Comparative Synthesis Example 4 was used. At this time, at the time of kneading, the dispersibility of each component was poor, and the discharge speed of the kneaded material was about 30% of that of the example. After the pulverization, a large amount of coarse powder was generated. When the same evaluation as in Example 1 was performed, it was found that the developing property and the fixing property were extremely poor.

[Effects of the Invention] In the toner of the present invention, problems related to the conventional toners are remarkably improved, excellent in anti-offset and anti-roller winding, wide fixing temperature range, and excellent pulverizability with excellent developing characteristics. A good toner can be obtained.

This is because, in a resin composition comprising a polyester resin and a vinyl resin which is uniformly mixed from a high molecular weight polymer component containing a crosslinked region to a low molecular weight polymer component, high molecular weight and low molecular weight It is thought that the segments are mixed together, and the high molecular weight component including crosslinks is
At the time of heat melting, the matrix prevents the cohesive strength from being lowered and excessive fluidity, while the low molecular weight component shows heat fusibility, so that it is heat-melted at a low temperature. It is considered that the composition exhibits excellent heat melting properties in which flow is suppressed. The polymer which is uniformly mixed from the low molecular weight component to the high crosslinking component referred to in the present invention,
When the toner is used to form the toner, it means that the image density is not reduced and fogging is practically not caused by repeated use which occurs in the case of a polymer mixed in a non-uniform manner.

Regarding the pulverizability, the high molecular domain component other than the crosslinked domain gives the composition toughness while the crosslinked domain component gives fragility, and the low molecular weight component gives the composition further easiness to be pulverized. It is thought that the pulverization characteristics required to improve the production efficiency are improved.

Furthermore, by including a polyester resin comprising a condensate of a polybasic acid component and a polyhydric alcohol component in the binder resin, a toner having excellent offset resistance, blocking resistance, and fixability can be obtained.

 ──────────────────────────────────────────────────続 き Continued on the front page (72) Inventor Hirohide Tanigawa 3-30-2 Shimomaruko, Ota-ku, Tokyo Inside Canon Inc. (72) Inventor Masaki Uchiyama 3-30-2 Shimomaruko, Ota-ku, Tokyo Canon (56) References JP-A-60-123850 (JP, A) JP-A-2-29664 (JP, A) JP-A-58-159546 (JP, A) JP-A-59-107359 (JP, A A)

Claims (2)

(57) [Claims] 1. A THF-insoluble content of 5 or more synthesized by polymerizing with one or more vinyl monomers.
% By weight, and in the molecular weight distribution of the THF-soluble component by GPC, a vinyl resin (A) having at least one peak in a molecular weight region of 2,000 to 15,000, and a polybasic acid component and a polyhydric alcohol component as monomers. Number average molecular weight of 1,500 to 10,000, synthesized by condensation polymerization using
Polymerization with a plurality of vinyl monomers and 0.01 to 5% by weight (based on the total weight of all other monomers) in the presence of a polyester resin (C) having 0 and a weight average molecular weight of 6,000 to 200,000. A vinyl resin (A) at the time of synthesis of the resin composition.
(A), the amount (B) of the plurality of vinyl monomers used, and the weight ratio of the amount (C) of the polyester resin (C) have the following relationship (A) :( B) :( C) = (10-35) :( 20-80):
(5 to 40), and the resin composition contains 5 to 50% by weight (based on the weight of the resin composition) of a THF-insoluble component. A resin composition for a toner, having at least one peak in a region of up to 20,000. 2. An electrostatic image developing toner containing at least a binder resin and a colorant, wherein the binder resin contains a THF-insoluble component synthesized by polymerization using one or more vinyl monomers. A vinyl-based resin (A) having an amount of less than 5% by weight and having at least one peak in the molecular weight region of 2,000 to 15,000 in the molecular weight distribution of THF-soluble GPC, and a polybasic acid component and a polyvalent monomer as monomers. Number average molecular weight 1,50 synthesized by condensation polymerization using alcohol component
Using a plurality of vinyl monomers and 0.01 to 5% by weight (based on the total weight of all other monomers) of a crosslinkable monomer in the presence of a polyester resin (C) having 0 to 10,000 and a weight average molecular weight of 6,000 to 200,000. A resin composition synthesized by polymerization, wherein the vinyl resin (A) is used during the synthesis of the resin composition.
(A), the amount (B) of the plurality of vinyl monomers used, and the weight ratio of the amount (C) of the polyester resin (C) have the following relationship (A) :( B) :( C) = (10-35) :( 20-80):
(5 to 40), and the resin composition contains 5 to 50% by weight (based on the weight of the resin composition) of a THF-insoluble component. An electrostatic image developing toner having at least one peak in an area of 20,00020,000.