JP2012103565A - Overcoat composition for electrophotography, electrophotography forming method and electrophotography forming device - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an overcoat composition for electrophotography that dose not reject a toner image on a recording medium, for instance, a toner image by toner including wax and has excellent adhesion therewith.SOLUTION: An overcoat composition for electrophotography used for overcoating a toner image created on a recording medium by an electrophotography method using toner, includes at least a compound expressed by the following general formula (1), where, in the general formula (1), Rrepresents either of a hydrogen atom or a methyl group.

Description

  The present invention relates to an electrophotographic overcoat composition, an electrophotographic forming method, and an electrophotographic forming apparatus used for overcoating a toner image on a recording medium.

  In recent years, changes and updates of information have become frequent, and systems that can output variable information such as changing and updating information one by one, and speeding up of print output have been desired. Printing is being used.

  As an apparatus used for on-demand printing, there are usually an electrophotographic system and an inkjet system, but an electrophotographic system using toner is mainly used. In the electrophotographic system, input image information is reproduced with toner.

Most conventional fixing devices used for fixing toners have a large amount of oil applied to the surface of a roller or the like in order to improve releasability.
However, the application of a large amount of oil to a roller or the like has problems such as oil contamination of the recording medium, cost increase, and a space for storing the oil, which makes the fixing device complicated and large.

Therefore, in recent years, it has become necessary to cope with an oilless mechanism for the purpose of simplifying the fixing device and preventing adverse effects on the image of oil (oil dirt, oil streaks, etc.).
For this reason, toners that do not require oil to be applied to the fixing roller, so-called oilless toners, have been tried. As the oilless toner, a toner containing a wax is generally proposed.

A catalog or cover produced by the on-demand printing may be provided with a transparent layer on the printing surface in order to protect it from water wetting and dirt, or to give gloss, depending on the application.
Examples of the method for applying a transparent layer to the printing surface include overcoat, vinyl drawing, press coat, and film sticking. These are performed after printing. Among these, overcoating with varnish is a simple method and is becoming mainstream.

As a technique related to the overcoat in the electrophotographic system, for example, as a varnish composition used for a printed material to which a fixing oil is applied, water-based that does not contain ammonia and has a low static surface tension. A varnish composition has been proposed (Patent Document 1).
In addition, a resin forming apparatus that forms a silicone resin layer on a printing surface to protect the printing surface, waterproof processing, and gloss, and an image forming apparatus including the device have been proposed (Patent Document 2).
Also, there has been proposed a metal container printing method that can efficiently perform high-mix low-volume printing by using an electrophotographic system, and protect a toner layer and impart gloss by performing varnishing (Patent Document 3). ).

  However, in these proposed techniques, the combination of the toner and the overcoat composition (varnish) is limited. Even when the overcoat composition can be applied onto the toner image on the recording medium, the adhesion between the toner image and the overcoat composition may be weakly peeled off. In particular, when a toner containing wax (oilless toner) is used as the toner, there is a remarkable problem that the adhesiveness is weak and the toner is peeled off, and further, there is a problem that the overcoat composition is repelled.

  Therefore, an electrophotographic overcoat composition having excellent adhesion without repelling a toner image on a recording medium, for example, a toner image containing a wax-containing toner, and the electrophotographic overcoat composition are used. At present, there is a need for an electrophotographic forming method and an electrophotographic forming apparatus.

  An object of the present invention is to solve the above-described problems and achieve the following objects. That is, the present invention relates to an electrophotographic overcoat composition having excellent adhesion without repelling a toner image on a recording medium, for example, a toner image containing a toner containing wax, and the electrophotographic overcoat. An object of the present invention is to provide an electrophotographic forming method and an electrophotographic forming apparatus using the composition.

Means for solving the problems are as follows. That is,
<1> An electrophotographic overcoat composition used for overcoating a toner image formed on a recording medium by an electrophotographic method using a toner, which contains at least a compound represented by the following general formula (1) This is an overcoat composition for electrophotography.
In the general formula (1), R ¹ represents a hydrogen atom or a methyl group.
<2> The overcoat composition for electrophotography according to <1>, which does not substantially contain an organic solvent having a boiling point of 200 ° C. or lower.
<3> The overcoat composition for electrophotography according to any one of <1> to <2>, wherein the content of the compound represented by the general formula (1) is 1% by mass to 50% by mass. .
<4> The electrophotographic overcoat composition according to any one of <1> to <3>, further containing a surfactant.
<5> The overcoat composition for electrophotography according to any one of <1> to <4>, which is a photocurable type.
<6> a charging step for charging the surface of the electrophotographic photosensitive member;
Exposing the charged surface of the electrophotographic photosensitive member imagewise to form an electrostatic latent image; and
Developing the electrostatic latent image with toner to form a toner image;
A transfer step of transferring the developed toner image to a recording medium;
An application step of applying an electrophotographic overcoat composition to the toner image on the transferred recording medium,
The electrophotographic overcoat composition is the electrophotographic overcoat composition according to any one of <1> to <5>.
<7> The electrophotographic forming method according to <6>, wherein the toner contains a wax.
<8> The electrophotographic forming method according to any one of <6> to <7>, wherein an average coating thickness of the overcoat composition is 1 μm to 15 μm.
<9> an electrophotographic photoreceptor;
Charging means for charging the surface of the electrophotographic photosensitive member;
Exposure means for imagewise exposing the surface of the charged electrophotographic photoreceptor to form an electrostatic latent image;
Developing means for developing the electrostatic latent image with toner to form a toner image;
Transfer means for transferring the developed toner image to a recording medium;
Application means for applying an electrophotographic overcoat composition to the toner image on the transferred recording medium,
The electrophotographic overcoat composition is the electrophotographic overcoat composition according to any one of <1> to <5>.
<10> The electrophotographic forming apparatus according to <9>, wherein the toner contains a wax.
<11> The electrophotographic forming apparatus according to any one of <9> to <10>, which forms a color image.

  According to the present invention, the above-described problems can be solved, and an electrophotographic overprint having excellent adhesion without repelling a toner image on a recording medium, for example, a toner image containing a wax-containing toner. A coating composition, and an electrophotographic forming method and an electrophotographic forming apparatus using the electrophotographic overcoat composition can be provided.

FIG. 1 is a structural diagram of normal paraffin. FIG. 2 is a structural diagram of isoparaffin. FIG. 3 is a schematic diagram illustrating an example of the application unit. FIG. 4 is a diagram showing an example of the image forming apparatus of the present invention. FIG. 5 is a diagram showing another example of the image forming apparatus of the present invention. FIG. 6 is a diagram showing the tandem developing device of FIG.

(Overcoat composition for electrophotography)
The electrophotographic overcoat composition of the present invention is an electrophotographic overcoat composition used for overcoating a toner image formed on a recording medium by an electrophotographic method using a toner, and has the following general formula (1) ) At least, and further contains other components as necessary.

<Compound represented by the general formula (1)>
The electrophotographic overcoat composition contains a compound represented by the following general formula (1).
In the general formula (1), R ¹ represents a hydrogen atom or a methyl group.

Examples of the compound represented by the general formula (1) include acryloylmorpholine and methacryloylmorpholine. Among these, acryloylmorpholine is preferable because it has a high curing rate and a high effect of improving adhesion.
The compound represented by the general formula (1) may be used alone or in combination of two or more.

  There is no restriction | limiting in particular as content of the compound represented by the said General formula (1) in the said overcoat composition for electrophotography, Although it can select suitably according to the objective, 1 mass%-50 mass% Is preferable, and 5 mass%-35 mass% is more preferable. When the content is less than 1% by mass, the adhesion may be inferior, and when it exceeds 50% by mass, the viscosity of the overcoat composition for electrophotography decreases or the image is dissolved and disturbed. Sometimes. When the content is within a more preferable range, it is advantageous in that adhesion is more excellent.

Although the compound represented by the general formula (1) has been conventionally used as a diluent for UV ink, it has been known so far that it has excellent characteristics when used in an overcoat composition for electrophotography. It wasn't.
The inventors of the present invention contain a compound represented by the general formula (1) in an overcoat of a toner image (electrophotographic image by toner) prepared on a recording medium by an electrophotographic method using toner. It has been found that when the electrophotographic overcoat composition is used, the compound represented by the general formula (1) exhibits excellent characteristics, and particularly improves adhesion.

Since electrophotographic toners in recent years generally contain a wax, when a conventional overcoat composition is used for the overcoat, the toner is repelled and the adhesion is insufficient. This tendency is particularly noticeable in toners containing low-polarity paraffin wax.
However, these problems can be solved by incorporating the compound represented by the general formula (1) into the overcoat composition.
The reason is that the compound represented by the general formula (1) has a high ability to dissolve the binder resin in the toner and can penetrate into the toner instantaneously.

<Other ingredients>
Examples of the other components include a polymerizable oligomer, a polymerizable unsaturated compound, a photopolymerization initiator, a sensitizer, a polymerization inhibitor, and a surfactant.

-Polymerizable oligomer-
There is no restriction | limiting in particular as said polymerizable oligomer, According to the objective, it can select suitably, For example, polyester acrylate, epoxy acrylate, urethane acrylate etc. are mentioned.
There is no restriction | limiting in particular as said polyester acrylate, According to the objective, it can select suitably, For example, the acrylic ester of the polyester polyol obtained from a polyhydric alcohol and a polybasic acid is mentioned. The polyester acrylate exhibits excellent reactivity.
There is no restriction | limiting in particular as said epoxy acrylate, According to the objective, it can select suitably, For example, the epoxy acrylate obtained by reaction of bisphenol-type epoxy, novolak-type epoxy, alicyclic epoxy, etc. and acrylic acid is mentioned. It is done. The epoxy acrylate is excellent in hardness, flexibility, and curability.
There is no restriction | limiting in particular as said urethane acrylate, According to the objective, it can select suitably, For example, the urethane acrylate obtained by reacting polyester polyol, polyether polyol, etc., acrylic acid ester with a diisocyanate and a hydroxyl group Is mentioned. When the urethane acrylate is used, a flexible and strong film can be obtained.
The said polymerizable oligomer may be used individually by 1 type, and may use 2 or more types together.

  There is no restriction | limiting in particular as content of the said polymerizable oligomer in the said overcoat composition for electrophotography, Although it can select suitably according to the objective, 5 mass%-60 mass% are preferable, and 10 mass%- 50 mass% is more preferable, and 20 mass%-45 mass% is especially preferable. When the content is less than 5% by mass, poor curing may occur, the viscosity may be too low, or the flexibility after curing may be impaired. When the content exceeds 60% by mass, the adhesion is deteriorated. Or the viscosity becomes too high. When the content is within the particularly preferable range, it is advantageous in terms of viscosity optimization, curability, flexibility of the coating layer after curing, and strength.

-Polymerizable unsaturated compound-
The polymerizable unsaturated compound is not particularly limited and may be appropriately selected depending on the intended purpose. For example, a monofunctional polymerizable unsaturated compound, a bifunctional polymerizable unsaturated compound, and a trifunctional polymerizable compound. Examples thereof include unsaturated compounds and tetrafunctional or higher polymerizable unsaturated compounds.
Examples of the monofunctional polymerizable unsaturated compound include 2-ethylhexyl acrylate, 2-hydroxylethyl acrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, benzyl acrylate, phenyl glycol monoacrylate, and cyclohexyl acrylate. It is done.
Examples of the bifunctional polymerizable unsaturated compound include 1,4-butanediol diacrylate, 1,6-hexanediol diacrylate, 1,9-nonanediol diacrylate, tripropylene glycol diacrylate, and tetraethylene glycol. Examples include diacrylate.
Examples of the trifunctional polymerizable unsaturated compound include trimethylolpropane triacrylate, pentaerythritol triacrylate, tris (2-hydroxyethyl) isocyanurate triacrylate, and the like.
Examples of the tetrafunctional or higher polymerizable unsaturated compound include pentaerythritol tetraacrylate, ditrimethylolpropane tetraacrylate, dipentaerythritol hydroxypentaacrylate, and dipentaerythritol hexaacrylate.
The said polymerizable unsaturated compound may be used individually by 1 type, and may use 2 or more types together.

  There is no restriction | limiting in particular as content of the said polymerizable unsaturated compound in the said overcoat composition for electrophotography, Although it can select suitably according to the objective, 35 mass%-90 mass% are preferable, and 45 mass % To 85% by mass is more preferable, and 50% to 75% by mass is particularly preferable. When the content is less than 35% by mass, the adhesion may be lowered or the viscosity may be excessively high. When the content exceeds 90% by mass, the curing may be poor or the viscosity may be excessively low. , The flexibility after curing may be impaired. When the content is within the particularly preferable range, it is advantageous in terms of viscosity optimization, curability, flexibility of the coating layer after curing, and strength.

A polyfunctional one is faster than a monofunctional one and has a faster curing speed and is suitable for high-speed fixing, but has a large volume shrinkage. In the case of a polymerizable unsaturated compound that greatly shrinks due to a curing reaction, curling is likely to occur. Therefore, it is desirable to use a polymerizable unsaturated compound having a volumetric shrinkage as low as possible and its polymer.
The polymerizable unsaturated compound preferably has a volume shrinkage of 15% or less.

P. of the polymerizable unsaturated compound and the polymerizable oligomer. I. I. There is no restriction | limiting in particular as (skin irritation), Although it can select suitably according to the objective, 1.0 or less is preferable. P. I. I. If it is 5.0 or more, irritation to the skin is too strong, which may cause safety problems. The compound represented by the general formula (1) is P.I. I. I. Is 0.5.
Further, the hue of the polymerizable unsaturated compound and the polymerizable oligomer is preferably as colorless and transparent as possible, and preferably 2 or less in the Gardner gray scale. When the Gardner gray scale exceeds 2, the color of the image portion may change, and the discoloration of the background portion may become conspicuous.

-Photopolymerization initiator-
The photopolymerization initiator is not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include benzophenone, benzoin ethyl ether, benzoin isopropyl ether, and benzyl. A commercial item can be used as said photoinitiator. Examples of the commercially available photopolymerization initiator include Irgacure 1300, Irgacure 369, Irgacure 907 manufactured by Ciba Specialty Chemicals, Inc., and Lucirin TPO manufactured by BASF.

  When the mixture of the polymerizable oligomer or the polymerizable unsaturated compound and the photopolymerization initiator is irradiated with ultraviolet rays, the photopolymerization initiator is represented by the following formulas (I) and (II): Generate radicals. The radical causes an addition reaction of the polymerizable oligomer or the polymerizable unsaturated compound to the polymerizable double bond. Further radicals are generated by the addition reaction, and by repeating the addition reaction to the polymerizable double bond of the other polymerizable oligomer or the polymerizable unsaturated compound, the polymerization reaction is performed as shown in the following formula (III). proceed.

(I) Hydrogen drawing type

(II) Photocleavage type

(III) Polymerization
The photopolymerization initiator includes (i) high ultraviolet absorption efficiency, (ii) high solubility in the polymerizable oligomer or polymerizable unsaturated compound, (iii) odor, yellowing, and toxicity. Those having good properties such as low and (iv) no dark reaction are preferred.

  There is no restriction | limiting in particular as content of the said photoinitiator in the said overcoat composition for electrophotography, Although it can select suitably according to the objective, 1 mass%-10 mass% are preferable, and 2 mass% is preferable. -5 mass% is more preferable.

-Sensitizer-
In the case of using the hydrogen abstraction type benzophenone photopolymerization initiator of the formula (I), the reaction may be slowed only by the photopolymerization initiator. It is preferable to improve the property. By containing an amine-based sensitizer, there is an effect of supplying hydrogen to the photopolymerization initiator by a hydrogen abstraction action and an effect of preventing reaction inhibition due to oxygen in the air.
The amine-based sensitizer is not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include triethanolamine, triisopropanolamine, 4,4-diethylaminobenzophenone, 2-dimethylaminoethylbenzoic acid. , Ethyl 4-dimethylaminobenzoate, isoacyl 4-dimethylaminobenzoate and the like.

  There is no restriction | limiting in particular as content of the said sensitizer in the said overcoat composition for electrophotography, Although it can select suitably according to the objective, 1 mass%-15 mass% are preferable, and 3 mass%- 8 mass% is more preferable.

-Polymerization inhibitor-
The polymerization inhibitor is used to increase the storage stability of the electrophotographic overcoat composition.
The polymerization inhibitor is not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include 2,6-ditert-butyl-p-cresol (BHT), 2,3-dimethyl-6-tert. -Butylphenol (IA), anthraquinone, hydroquinone (HQ), hydroquinone monomethyl ether (MEHQ) and the like.

  There is no restriction | limiting in particular as content of the said polymerization inhibitor in the said overcoat composition for electrophotography, Although it can select suitably according to the objective, 0.005 mass%-3 mass% are preferable.

-Surfactant-
By including the surfactant in the electrophotographic overcoat composition, adsorptivity is imparted to the interface between the toner and the overcoat composition, or the surface tension of the overcoat composition is lowered, and wettability is improved. To do.
There is no restriction | limiting in particular as said surfactant, According to the objective, it can select suitably, For example, anionic surfactant, nonionic surfactant, silicone surfactant, fluorosurfactant etc. are mentioned.
Examples of the anionic surfactant include sulfosuccinate, disulfonate, phosphate ester, sulfate, sulfonate, and mixtures thereof.
Examples of the nonionic surfactant include polyvinyl alcohol, polyacrylic acid, isopropyl alcohol, acetylenic diol, ethoxylated octylphenol, ethoxylated branched secondary alcohol, bellfluorobutane sulfonate, alkoxylated alcohol, and the like. .
Examples of the silicone surfactant include polyether-modified poly-dimethyl-siloxane.
Examples of the fluorosurfactant include ethoxylated nonylphenol.

  There is no restriction | limiting in particular as content of the said surfactant in the said overcoat composition for electrophotography, Although it can select suitably according to the objective, 0.1 mass%-5 mass% are preferable, and 0. 5 mass%-3 mass% are more preferable. When the content is less than 0.1% by mass, wettability may not be obtained, and when it exceeds 5% by mass, curability may be inhibited. When the content is within the more preferable range, it is advantageous in terms of improving wettability.

  The other components further include leveling agents, matting agents, waxes for adjusting film physical properties, tackifiers (adhesives that do not inhibit polymerization) to improve adhesion to recording media such as polyolefin and PET. Property-imparting agent).

The electrophotographic overcoat composition preferably contains substantially no organic solvent having a boiling point of 200 ° C. or less from the viewpoint of preventing environmental influences caused by VOC (volatile organic compounds).
Here, the boiling point means a boiling point at 1 atmosphere.
In addition, the fact that the organic solvent having a boiling point of 200 ° C. or less is substantially free means that the content of the organic solvent having a boiling point of 200 ° C. or less in the electrophotographic overcoat composition is 0.1% by mass or less. Say. The content of the organic solvent having a boiling point of 200 ° C. or lower in the overcoat composition for electrophotography is, for example, increased to 260 ° C. at a temperature increase rate of 10 ° C./min according to the gas chromatograph method of JISK5601-5-1. It can be confirmed according to the conditions.
If the said content is 0.1 mass% or less, it is thought that the environmental influence by VOC hardly arises.

There is no restriction | limiting in particular as a viscosity of the said overcoat composition for electrophotography, Although it can select suitably according to the objective, The viscosity in 25 degreeC is 10 mPa * s-800 mPa * s. If the viscosity is less than 10 mPa · s or exceeds 800 mPa · s, it may be difficult to control the coating thickness.
The viscosity can be measured by, for example, a B-type viscometer (manufactured by Toyo Seiki Seisakusho).

  The electrophotographic overcoat composition can be prepared in an oil-based type using a solvent, but in the case of an ultraviolet curable type (photo-curable type) using UV, ensuring safety, environmental protection, energy saving and high It is preferable from the viewpoint of productivity.

<Toner>
The toner used in the electrophotographic method is not particularly limited and can be appropriately selected depending on the purpose. For example, the toner contains at least a binder resin and a colorant, preferably wax, and further if necessary. And toners containing other components.

-Binder resin-
There is no restriction | limiting in particular as said binder resin, According to the objective, it can select suitably, For example, styrene, such as polystyrene, poly p-styrene, polyvinyltoluene, or the homopolymer of its substitution, styrene-p- Chlorstyrene copolymer, styrene-propylene copolymer, styrene-vinyltoluene copolymer, styrene-methyl acrylate copolymer, styrene-ethyl acrylate copolymer, styrene-methacrylic acid copolymer, styrene- Methyl methacrylate copolymer, styrene-ethyl methacrylate copolymer, styrene-butyl methacrylate copolymer, styrene-α-chloromethacrylate methyl copolymer, styrene-acrylonitrile copolymer, styrene- Vinyl methyl ether copolymer, styrene-vinyl methyl ketone copolymer, Styrene copolymers such as len-butadiene copolymer, styrene-isopropyl copolymer, styrene-maleic acid ester copolymer, polythyme methacrylate resin, polybutyl methacrylate resin, polyvinyl chloride resin, polyvinyl acetate resin , Polyethylene resin, polyester resin, polyurethane resin, epoxy resin, polyvinyl butyral resin, polyacrylic acid resin, rosin resin, modified rosin resin, terpene resin, phenol resin, aliphatic or aromatic hydrocarbon resin, aromatic petroleum resin, etc. Is mentioned. These may be used individually by 1 type and may use 2 or more types together. Among these, it is particularly preferable to use a polyester resin because of its affinity with the recording medium to be fixed.

As a component which comprises the said polyester resin, a bivalent alcohol component, a trihydric or more polyhydric alcohol component, an acid component, etc. are mentioned, for example.
Examples of the divalent alcohol component include ethylene glycol, propylene glycol, 1,3-butanediol, 1,4-butanediol, 2,3-butanediol, diethylene glycol, triethylene glycol, and 1,5-pentanediol. 1,6-hexanediol, neopentyl glycol, 2-ethyl-1,3-hexanediol, hydrogenated bisphenol A, or diol obtained by polymerizing cyclic ether such as ethylene oxide or propylene oxide to bisphenol A, Etc.
Examples of the trihydric or higher polyhydric alcohol component include sorbitol, 1,2,3,6-hexanetetrol, 1,4-sorbitan, pentaerythritol, dipentaerythritol, tripentaerythritol, 1,2,4. -Butanetriol, 1,2,5-pentatriol, glycerol, 2-methylpropanetriol, 2-methyl-1,2,4-butanetriol, trimethylolethane, trimethylolpropane, 1,3,5-trihydroxy Benzene, etc.

Examples of the acid component include benzene dicarboxylic acids such as phthalic acid, isophthalic acid, and terephthalic acid, or anhydrides thereof, alkyl dicarboxylic acids such as succinic acid, adipic acid, sebacic acid, azelaic acid, or anhydrides thereof, and maleic acid. Unsaturated dibasic acids such as citraconic acid, itaconic acid, alkenyl succinic acid, fumaric acid and mesaconic acid, maleic anhydride, citraconic anhydride, itaconic anhydride, alkenyl succinic anhydride, etc. Examples thereof include acid anhydrides and trivalent or higher polyvalent carboxylic acid components.
Examples of the trivalent or higher polyvalent carboxylic acid component include trimellitic acid, pyrometic acid, 1,2,4-benzenetricarboxylic acid, 1,2,5-benzenetricarboxylic acid, and 2,5,7-naphthalenetricarboxylic acid. Acid, 1,2,4-naphthalenetricarboxylic acid, 1,2,4-butanetricarboxylic acid, 1,2,5-hexanetricarboxylic acid, 1,3-dicarboxy-2-methyl-2-methylenecarboxypropane, tetra (Methylenecarboxy) methane, 1,2,7,8-octanetetracarboxylic acid, emporic trimer acid, or their anhydrides, partial lower alkyl esters, and the like.

--Modified polyester capable of reacting with active hydrogen group-containing compound--
The binder resin may contain a modified polyester (prepolymer) that can react with the active hydrogen group-containing compound. The active hydrogen group-containing compound acts as an elongation agent, a crosslinking agent, or the like when the modified polyester capable of reacting with the active hydrogen group-containing compound undergoes an elongation reaction, a crosslinking reaction, or the like in the toner production process. The modified polyester capable of reacting with the active hydrogen group-containing compound undergoes an extension reaction to increase the molecular weight, whereby the heat-resistant storage stability of the toner and the stickiness of the image after fixing can be effectively reduced. In this case, the modified polyester capable of reacting with the active hydrogen group-containing compound is not particularly limited as long as it can react with the active hydrogen group-containing compound, and can be appropriately selected according to the purpose, for example, an isocyanate group, an epoxy group , Modified polyester having a carboxylic acid, an acid chloride group, and the like. Among these, a modified polyester containing an isocyanate group is preferable.

  The active hydrogen group-containing compound is not particularly limited as long as it has an active hydrogen group and can be appropriately selected according to the purpose. However, the modified polyester capable of reacting with the active hydrogen group-containing compound is an isocyanate group. In the case of the content-modified polyester, amines are preferable in that the molecular weight can be increased by a reaction such as an extension reaction or a crosslinking reaction with the isocyanate group-containing modified polyester.

  There is no restriction | limiting in particular as said amines, According to the objective, it can select suitably, For example, phenylenediamine, diethyltoluenediamine, 4,4'-diaminodiphenylmethane, 4,4'-diamino-3,3 ' -Dimethyldicyclohexylmethane, diaminecyclohexane, isophoronediamine, ethylenediamine, tetramethylenediamine, hexamethylenediamine, diethylenetriamine, triethylenetetramine, ethanolamine, hydroxyethylaniline, aminoethyl mercaptan, aminopropyl mercaptan, aminopropionic acid, aminocaproic acid, etc. Is mentioned. In addition, ketimine compounds, oxazolidone compounds, and the like in which these amino groups are blocked with ketones (acetone, methyl ethyl ketone, methyl isobutyl ketone, etc.) may be mentioned.

-Colorant-
The colorant is not particularly limited and may be appropriately selected from known dyes and pigments according to the purpose. 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, Lead Red, Lead Red, Cadmium Red, Cad Muum Mercury Red, Antimon Zhu, Permanent Red 4R, PA Red, Faise Red, Parachlor Ortho Nitroaniline Red, Resol Fast Scarlet G, Brilliant Fast Scarlet, Brilliant Carmine BS, Permanent Red (F2R, F4R, FRL, FRLL, F4RH), Fast Scarlet VD, Belkan Fast Rubin B, Brilliant Scarlet G, Risor Rubin GX, Permanent Red F5R, Brilliant Carmine 6B, Pigment Scarlet 3B, Bordeaux 5B, Toluidine Maroon, Permanent Bordeaux F2K, Helio Bordeaux BL, Bordeaux 10B, Bon Maroon Light, Bon Maroon Medium, Eosin Lake B, Rhodamine Lake Y, Alizarin Lake, Thioindigo Red B, Thioindigo Maroon, Oh Lured, Quinacridone Red, Pyrazolone 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, Indanthrene Blue (RS, BC), Indigo, Ultramarine Blue, Bitumen, Anthraquinone Blue, Fast Violet B, Methyl Violet Lake, Cobalt Purple, Manganese Purple, Dioxane Violet, Anthraquinone Violet, Chrome Green, Zinc Green, Oxidation Chrome, Pyridian, Emerald Green, Pigment Green B, Naphthol Green B, Green Gold, Ash Examples include degreen lake, malachite green lake, phthalocyanine green, anthraquinone green, titanium oxide, zinc white, and litbon. These may be used individually by 1 type and may use 2 or more types together.

  There is no restriction | limiting in particular as content of the said coloring agent, Although it can select suitably according to the objective, 1 mass part-15 mass parts are preferable with respect to 100 mass parts of said toners, and 3 mass parts-10 parts. Part by mass is more preferable.

  The colorant may be used as a master batch combined with a resin. The resin is not particularly limited and may be appropriately selected from known ones according to the purpose. For example, styrene or a substituted polymer thereof, styrene copolymer, polymethyl methacrylate resin, polybutyl Methacrylate resin, polyvinyl chloride resin, polyvinyl acetate resin, polyethylene resin, polypropylene resin, polyester resin, epoxy resin, epoxy polyol resin, polyurethane resin, polyamide resin, polyvinyl butyral resin, polyacrylic acid resin, rosin, modified rosin, terpene Examples thereof include resins, aliphatic hydrocarbon resins, alicyclic hydrocarbon resins, aromatic petroleum resins, chlorinated paraffins, and paraffins. These may be used individually by 1 type and may use 2 or more types together.

-Wax-
There is no restriction | limiting in particular as said wax, Although it can select suitably according to the objective, Petroleum-type wax is preferable at a point with a high mold release capability. Examples of the petroleum wax include paraffin wax, microcrystalline wax, and mixed wax of paraffin wax and microcrystalline wax.

  The wax preferably contains 10% by mass or more of hydrocarbon component isoparaffin from the viewpoint of adhesion to the electrophotographic overcoat composition.

  The molecular weight of the wax is not particularly limited and may be appropriately selected depending on the intended purpose. However, the molecular weight of the component that contributes to the adhesion of the electrophotographic overcoat composition is high, and the molecular weight is preferably as close as possible. Specifically, the average molecular weight is preferably 500 or more from the viewpoint of adhesion with the overcoat composition for electrophotography.

  The mass% of isoparaffin in the wax and the average molecular weight of the wax can be measured by, for example, FD (Field Desorption) method using JMS-T100GC “AccuTOF GC”.

  FIG. 1 shows a structural diagram of normal paraffin. FIG. 2 shows a structural diagram of isoparaffin. Normal paraffin has a linear structure, and isoparaffin has a branched structure. The linear structure has little molecular bias and small polarity. On the other hand, the branched chain structure is molecularly biased and is more polar than normal paraffin. The higher the polarity, the better the wettability of the overcoat composition.

  There is no restriction | limiting in particular as melting | fusing point of the said wax, Although it can select suitably according to the objective, 40 to 160 degreeC is preferable and 50 to 120 degreeC is more preferable. When the melting point is less than 40 ° C., the heat resistant storage stability may be adversely affected. When the melting point exceeds 160 ° C., cold offset may easily occur during fixing at a low temperature.

  There is no restriction | limiting in particular as melt viscosity of the said wax, Although it can select suitably according to the objective, 5 cps-1,000 cps are preferable at the temperature 20 degreeC higher than melting | fusing point, and 10 cps-100 cps are more preferable. When the melt viscosity exceeds 1,000 cps, the effect of improving hot offset resistance and low-temperature fixability may be poor.

  There is no restriction | limiting in particular as content of the said wax in the said toner, Although it can select suitably according to the objective, 0 mass%-40 mass% are preferable, and 3 mass%-30 mass% are more preferable.

-Other ingredients-
Examples of the other components include a charge control agent, a magnetic material, and an external additive.

-Charge control agent-
There is no restriction | limiting in particular as said charge control agent, According to the positive / negative of the electric charge charged to a photoreceptor, it can select and use a positive or negative charge control agent suitably.
---- Negative charge control agent ---
Examples of the negative charge control agent include a resin or compound having an electron donating functional group, an azo dye, a metal complex of an organic acid, and the like.
Examples of commercially available negative charge control agents include Bontron (product numbers: S-31, S-32, S-34, S-36, S-37, S-39, S-40, S-44, E-81, E-82, E-84, E-86, E-88, A, 1-A, 2-A, 3-A) (all manufactured by Orient Chemical Co., Ltd.), Kaya Charge (product number) : N-1, N-2), Kaya set black (product number: T-2, 004) (all manufactured by Nippon Kayaku Co., Ltd.); Eisenspiron black (T-37, T-77, T-95) , TRH, TNS-2) (all manufactured by Hodogaya Chemical Co., Ltd.); FCA-1001-N, FCA-1001-NB, FCA-1001-NZ (all manufactured by Fujikura Kasei Co., Ltd.), etc. Is mentioned. These may be used individually by 1 type and may use 2 or more types together.

--- Positive charge control agent ---
Examples of the positive charge control agent include basic compounds such as nigrosine dyes; cationic compounds such as quaternary ammonium salts; and metal salts of higher fatty acids.
Commercially available products of the positive charge control agent include, for example, Bontron (product numbers: N-01, N-02, N-03, N-04, N-05, N-07, N-09, N-10, N-11, N-13, P-51, P-52, AFP-B) (all manufactured by Orient Chemical Co., Ltd.); TP-302, TP-415, TP-4040 (all Hodogaya Chemical) Manufactured by Kogyo Co., Ltd.); copy blue PR, copy charge (product numbers: PX-VP-435, NX-VP-434) (both manufactured by Hoechst); FCA (product numbers: 201, 201-B-1, 201-) B-2, 201-B-3, 201-PB, 201-PZ, 301) (all manufactured by Fujikura Kasei Co., Ltd.); PLZ (part numbers: 1001, 2001, 6001, 7001) (all Shikoku Chemical Industries) Etc.) It is below. These may be used individually by 1 type and may use 2 or more types together.

  The content of the charge control agent is not particularly limited and can be appropriately selected according to the type of the binder resin, the toner production method including the dispersion method, and the like, and is 0 for 100 parts by mass of the binder resin. 1 mass part-10 mass parts are preferable, and 0.2 mass part-5 mass parts are more preferable. When the content exceeds 10 parts by mass, the chargeability of the toner is too high, the effect of the charge control agent is reduced, the electrostatic attraction with the developing roller is increased, and the flowability of the electrophotographic developer is reduced. If the amount is less than 0.1 part by mass, the charging start-up property and the charge amount may not be sufficient, and the toner image may be easily affected.

--- Magnetic material--
Examples of the magnetic material include (1) magnetic iron oxide such as magnetite, maghemite, and ferrite, or iron oxide containing other metal oxides, (2) metals such as iron, cobalt, and nickel, or these metals. And alloys of aluminum, cobalt, copper, lead, magnesium, tin, zinc, antimony, beryllium, bismuth, cadmium, calcium, manganese, selenium, titanium, tungsten, vanadium, etc. (3) or mixtures thereof, etc. Is used.

Examples of the magnetic material include Fe ₃ O ₄ , γ-Fe ₂ O ₃ , ZnFe ₂ O ₄ , Y ₃ Fe ₅ O ₁₂ , CdFe ₂ O ₄ , Gd ₃ Fe ₅ O ₁₂ , CuFe ₂ O ₄ , and PbFe _12. Examples thereof include O, NiFe ₂ O ₄ , NdFe ₂ O, BaFe ₁₂ O ₁₉ , MgFe ₂ O ₄ , MnFe ₂ O ₄ , LaFeO ₃ , iron powder, cobalt powder, and nickel powder. These may be used individually by 1 type and may be used in combination of 2 or more type. Among these, fine powders of iron trioxide and γ-iron trioxide are particularly preferable.

There is no restriction | limiting in particular as content of the said magnetic body, Although it can select suitably according to the objective, 10 mass parts-200 mass parts are preferable with respect to 100 mass parts of said binder resins, 20 mass parts -150 mass parts is more preferable.
The magnetic material can also be used as a colorant.

--External additive--
Examples of the external additive include inorganic fine particles for imparting fluidity, heat resistant storage stability, developability, transferability, chargeability, and the like to the toner.
Examples of the inorganic fine particles include silica, titania, alumina, cerium oxide, strontium titanate, calcium carbonate, magnesium carbonate, and calcium phosphate. Further, silica fine particles hydrophobized with silicone oil or hexamethyldisilazane, titanium oxide with a specific surface treatment, and the like can be given.
Examples of commercially available silica fine particles include Aerosil (part numbers: 130, 200 V, 200 CF, 300, 300 CF, 380, OX50, TT600, MOX80, MOX170, COK84, RX200, RY200, R972, R974, R976, R805, R811. , R812, T805, R202, VT222, RX170, RXC, RA200, RA200H, RA200HS, RM50, RY200, REA200) (all manufactured by Nippon Aerosil Co., Ltd.), HDK (part number: H20, H2000, H3004, H2000 / 4, H2050EP, H2015EP, H3050EP, KHD50), HVK2150 (all manufactured by Wacker Chemical Co., Ltd.), cabozil (part numbers: L-90, LM-130, LM-150, M-5) PTG, MS-55, H-5, HS-5, EH-5, LM-150D, M-7D, MS-75D, TS-720, TS-610, TS-530 (all manufactured by Cabot Corporation) Etc.
These may be used alone or in combination of two or more.
The content of the inorganic fine particles is preferably 0.1 parts by mass to 5.0 parts by mass, and more preferably 0.8 parts by mass to 3.2 parts by mass with respect to 100 parts by mass of the toner.

The toner preferably has an average circularity of 0.93 to 1.00, which is an average value of the circularity SR represented by the following formula 1, and more preferably 0.95 to 0.99. This average circularity is an index of the degree of unevenness of the toner particles, and indicates 1.00 when the toner is a perfect sphere, and the average circularity becomes smaller as the surface shape becomes more complicated.
<Formula 1>
Circularity SR = (perimeter of circle having the same area as the projected area of toner particles) / (perimeter of projected image of toner particles)

  When the average circularity is in the range of 0.93 to 1.00, the surface of the toner particles is smooth, and the toner particles and the contact area between the toner particles and the photosensitive member are small, so that the transferability is excellent. Further, since the toner particles have no corners, the developer agitation torque in the developing device is small, and the agitation drive is stabilized, so that no abnormal image is generated. In addition, since there are no angular toner particles in the toner that forms the dots, the pressure is uniformly applied to the entire toner that forms the dots when pressed against the recording medium during transfer, and the transfer is not easily lost. Further, since the toner particles are not angular, the abrasive power of the toner particles themselves is small, and the surface of the image carrier is not damaged or worn.

The circularity SR can be measured using, for example, a flow type particle image analyzer (manufactured by Toa Medical Electronics Co., Ltd., FPIA-1000).
First, 0.1 mL to 0.5 mL of a surfactant (preferably alkylbenzene sulfonate) is added as a dispersant to 100 mL to 150 mL of water from which impure solids have been previously removed, and 0.1 g of a measurement sample is further added. Add ~ 0.5g. The suspension in which the sample is dispersed is subjected to a dispersion treatment with an ultrasonic disperser for about 1 to 3 minutes, and the dispersion concentration is set to 3,000 / μL to 10,000 / μL. Measure.

  The toner has a volume average particle diameter of preferably 3 μm to 10 μm, more preferably 4 μm to 8 μm. In this range, since the toner particles have a sufficiently small particle size with respect to the minute latent image dots, the dot reproducibility is excellent. When the volume average particle size is less than 3 μm, phenomena such as a decrease in transfer efficiency and a decrease in blade cleaning properties may easily occur. When the volume average particle size exceeds 10 μm, it may be difficult to suppress scattering of characters and lines.

Here, the volume average particle diameter of the toner can be measured, for example, by a Coulter counter method. Examples of the measuring device for the particle size distribution of toner particles by the Coulter counter method include Coulter Counter TA-II and Coulter Multisizer II (both manufactured by Coulter).
First, 0.1 mL to 5 mL of a surfactant (preferably alkyl benzene sulfonate) is added as a dispersant to 100 mL to 150 mL of the electrolytic aqueous solution. Here, the electrolytic solution is a solution prepared by preparing a 1% NaCl aqueous solution using primary sodium chloride. For example, ISOTON-II (manufactured by Coulter) can be used. Here, 2 mg to 20 mg of a measurement sample is further added. The electrolytic solution in which the sample is suspended is subjected to a dispersion treatment with an ultrasonic disperser for about 1 to 3 minutes, and the volume and the number of toner particles or toner are measured with the measurement apparatus using a 100 μm aperture as the aperture. Calculate volume distribution and number distribution. From the obtained distribution, the volume average particle diameter of the toner can be obtained.
Channels are 2.00 μm to less than 2.52 μm; 2.52 μm to less than 3.17 μm; 3.17 μm to less than 4.00 μm; 4.00 μm to less than 5.04 μm; 5.04 μm to less than 6.35 μm; .35 μm to less than 8.00 μm; 8.00 μm to less than 10.08 μm; 10.08 μm to less than 12.70 μm; 12.70 μm to less than 16.00 μm; 16.00 μm to less than 20.20 μm; Use less than 40 μm; 25.40 μm to less than 32.00 μm; 13 channels of 32.00 μm to less than 40.30 μm, and target particles with a particle size of 2.00 μm to less than 40.30 μm.

-Toner production method-
The method for producing the toner is not particularly limited and may be appropriately selected depending on the intended purpose. For example, a pulverization method, a monomer composition containing a specific polymerizable monomer is directly added in an aqueous phase. Polymerization method (suspension polymerization method, emulsion polymerization method), a method of emulsifying or dispersing a specific binder resin solution in an aqueous medium, a method of dissolving with a solvent, desolvating and pulverizing, a melt spray method Etc.

--- Pulverization method--
The pulverization method is a method of obtaining the toner by, for example, melting and kneading a toner material, pulverizing, classifying, and the like.
In the case of the pulverization method, the shape may be controlled by applying a mechanical impact force to the obtained toner for the purpose of increasing the average circularity of the toner. In this case, the mechanical impact force can be applied to the toner using an apparatus such as a hybridizer or mechanofusion.
In the melting and kneading of the toner material, the toner material is mixed, and the mixture is charged into a melt kneader and melt kneaded. Examples of the melt kneader include a uniaxial continuous kneader, a biaxial continuous kneader, and a batch kneader using a roll mill. For example, KTK type twin screw extruder manufactured by Kobe Steel Co., Ltd., TEM type extruder manufactured by Toshiba Machine Co., Ltd., twin screw extruder manufactured by Casey Kay Co., Ltd., PCM type twin screw extruder manufactured by Ikegai Iron Works, Inc. A manufactured kneader or the like is preferably used. This melt-kneading is preferably performed under appropriate conditions so as not to cause the molecular chains of the binder resin to be broken. Specifically, the melt kneading temperature is performed with reference to the softening point of the binder resin. If the temperature is higher than the softening point, cutting is severe, and if the temperature is too low, dispersion may not proceed.

In the pulverization, the kneaded product obtained by the kneading is pulverized. In this pulverization, it is preferable that the kneaded material is first coarsely pulverized and then finely pulverized. In this case, a method of pulverizing by colliding with a collision plate in a jet stream, pulverizing particles by colliding with each other in a jet stream, or pulverizing in a narrow gap between a mechanically rotating rotor and a stator is preferably used. .
In the classification, the pulverized product obtained by the pulverization is classified and adjusted to particles having a predetermined particle diameter. The classification can be performed, for example, by removing the fine particle portion by a cyclone, a decanter, centrifugation, or the like.
After the pulverization and classification are completed, the pulverized product is classified in an air stream by centrifugal force or the like to produce a toner having a predetermined particle size.

--Suspension polymerization method--
The suspension polymerization method will be described later in an aqueous medium in which a colorant, a release agent, and the like are dispersed in an oil-soluble polymerization initiator and a polymerizable monomer, and a surfactant and other solid dispersant are contained. Emulsified and dispersed by an emulsification method. Thereafter, a polymerization reaction is performed to form particles, thereby obtaining the toner.
Examples of the polymerizable monomer include acrylic acids, methacrylic acid, α-cyanoacrylic acid, α-cyanomethacrylic acid, itaconic acid, crotonic acid, fumaric acid, maleic acid, maleic anhydride, and other acids, acrylamide, methacrylic acid, and the like. Functional groups on the surface of toner particles by partially using amide, diacetone acrylamide or their methylol compounds, vinyl pyridine, vinyl pyrrolidone, vinyl imidazole, ethyleneimine, acrylates with methacrylates such as dimethylaminoethyl methacrylate, methacrylates, etc. Can be introduced.
Further, by selecting a dispersant having an acid group or a basic group as the dispersant to be used, the dispersant can be adsorbed and left on the toner surface to introduce a functional group.

--Emulsion polymerization method--
As the emulsion polymerization method, a water-soluble polymerization initiator and a polymerizable monomer are emulsified in water using a surfactant, and a latex is synthesized by a usual emulsion polymerization method. Separately, a dispersion in which a colorant, a release agent and the like are dispersed in an aqueous medium is prepared, and after mixing, the toner is aggregated to a toner size and heat-fused to obtain a toner. A functional group can be introduced into the toner surface by using a latex similar to the monomer used in the suspension polymerization method.

--Method of emulsifying or dispersing a specific binder resin solution in an aqueous medium--
As a method for emulsifying or dispersing a specific binder resin solution in the aqueous medium, a solution or dispersion of a toner material having at least a binder resin is emulsified or dispersed in an aqueous medium, and the emulsion or dispersion is obtained. After the toner is prepared, the toner is granulated (aqueous granulation). As this method, for example, the following steps [1] to [4] are included.

<< Step [1]: Preparation of Solution or Dispersion of Toner Material >>
The solution or dispersion of the toner material is prepared by dissolving or dispersing a toner material such as a colorant and a binder resin in an organic solvent. The organic solvent is removed during or after the toner granulation.

<<< Step [2]: Preparation of aqueous medium >>>
The aqueous medium is not particularly limited and may be appropriately selected from known ones. For example, water, alcohol miscible with water, dimethylformamide, tetrahydrofuran, cellosolves, solvents such as lower ketones, or the like Examples thereof include a mixture thereof. Among these, water is particularly preferable.
The aqueous medium can be prepared, for example, by dispersing a dispersion stabilizer such as resin fine particles in the aqueous medium. The amount of the resin fine particles added to the aqueous medium is not particularly limited and may be appropriately selected depending on the intended purpose. For example, 0.5 mass% to 10 mass% is preferable.
The resin fine particle is not particularly limited as long as it is a resin that can form an aqueous dispersion in an aqueous medium, and can be appropriately selected from known resins according to the purpose, and may be a thermoplastic resin. It may be a thermosetting resin, for example, vinyl resin, polyurethane resin, epoxy resin, polyester resin, polyamide resin, polyimide resin, silicon resin, phenol resin, melamine resin, urea resin, aniline resin, ionomer resin, polycarbonate resin. , Etc. These may be used individually by 1 type and may use 2 or more types together. Among these, it is preferably formed of at least one selected from a vinyl resin, a polyurethane resin, an epoxy resin, and a polyester resin because an aqueous dispersion of fine spherical resin fine particles can be easily obtained.
In addition, in the aqueous medium, if necessary, from the viewpoint of stabilizing the oil droplets of the solution or dispersion at the time of emulsification or dispersion described later, and sharpening the particle size distribution while obtaining a desired shape, It is preferable to use a dispersant. There is no restriction | limiting in particular as said dispersing agent, According to the objective, it can select suitably, For example, surfactant, a sparingly water-soluble inorganic compound dispersing agent, a polymeric protective colloid, etc. are mentioned. These may be used individually by 1 type and may use 2 or more types together. Among these, surfactants are particularly preferable.

<<< Step [3]: Emulsification or Dispersion >>>
When the solution or dispersion containing the toner material is emulsified or dispersed in the aqueous medium, the solution or dispersion containing the toner material is preferably dispersed while stirring in the aqueous medium. The dispersion method is not particularly limited, but a batch type emulsifier such as a homogenizer (manufactured by IKA), polytron (manufactured by Kinematica), TK auto homomixer (manufactured by Tokushu Kika Kogyo Co., Ltd.), Ebara Milder (manufactured by Aihara Seisakusho), TK Fillmix, TK Pipeline Homomixer (made by Tokushu Kika Kogyo Co., Ltd.), Colloid Mill (made by Shinko Pantech Co., Ltd.), Thrasher, Trigonal Wet Fine Crusher (Mitsui Miike Chemical Industries) Co., Ltd.), Capitoron (Eurotech Co., Ltd.), Fine Flow Mill (Pacific Kiko Co., Ltd.) and other continuous emulsifiers, Microfluidizer (Mizuho Kogyo Co., Ltd.), Nanomizer (Nanomizer Co., Ltd.), APV Gaulin High-pressure emulsifiers (made by Gaulin), membrane emulsifiers such as membrane emulsifiers (made by Chilling Industries Co., Ltd.), Bro mixer (Hiyaka Kogyo Co., Ltd.) vibration type emulsifying machine such as, ultrasonic emulsifier such as an ultrasonic homogenizer (manufactured by Branson Co., Ltd.), and the like. Among these, APV Gaurin, homogenizer, TK auto homomixer, Ebara milder, TK fill mix, and TK pipeline homomixer are particularly preferable from the viewpoint of uniform particle size.
In the case where the binder resin contained in the solution or dispersion contains a modified polyester capable of reacting with an active hydrogen group-containing compound, the reaction proceeds during emulsification or dispersion. The reaction conditions are not particularly limited and can be appropriately selected according to the combination of the polymer capable of reacting with the active hydrogen group-containing compound and the active hydrogen group-containing compound. The reaction time is 10 minutes to 40 hours is preferable, and 2 hours to 24 hours is more preferable.

<< Step [4]: Removal of solvent >>
Next, the organic solvent is removed from the emulsified slurry obtained by the emulsification or dispersion. The organic solvent is removed by (1) a method in which the temperature of the entire reaction system is gradually raised to completely evaporate and remove the organic solvent in the oil droplets, and (2) the emulsion dispersion is sprayed in a dry atmosphere, Examples thereof include a method in which the water-insoluble organic solvent in the droplets is completely removed to form toner fine particles, and the aqueous dispersant is removed by evaporation.

<Recording medium>
The recording medium used in the electrophotographic method is not particularly limited as long as it can fix the toner, and can be appropriately selected according to the purpose.
There is no restriction | limiting in particular as a form of the said recording medium, Although it can select suitably according to the objective, In addition to a sheet form, the solid thing which has a plane and a curved surface may be sufficient. The recording medium may be, for example, a medium in which transparent toner is uniformly fixed on a medium such as paper and the paper surface is protected (so-called varnish coat). The material of the recording medium is not particularly limited and may be appropriately selected according to the purpose. For example, a general fiber constituting paper, cloth, etc., a plastic such as an OHP sheet having a liquid permeable layer Examples include films, metals, resins, and ceramics.

(Electrophotographic forming method and electrophotographic forming apparatus)
The electrophotographic forming method of the present invention includes at least a charging step, an exposure step, a development step, a transfer step, and a coating step, and other steps appropriately selected as necessary, for example, a static elimination step, Including a cleaning process and a recycling process. The charging process and the exposure process may be collectively referred to as an electrostatic latent image forming process.
The electrophotographic forming apparatus of the present invention includes an electrophotographic photosensitive member, a charging unit, an exposure unit, a developing unit, a transfer unit, and a coating unit. Means, for example, static elimination means, cleaning means, and recycling means. The charging unit and the exposure unit may be collectively referred to as an electrostatic latent image forming unit. As the electrophotographic photoreceptor, the electrophotographic photoreceptor of the present invention is used.
The electrophotographic forming method of the present invention can be preferably carried out by the electrophotographic forming apparatus of the present invention.
The charging step is performed by the charging unit, the exposure step is performed by the exposure unit, the development step is performed by the developing unit, the transfer step is performed by the transfer unit, the coating step is performed by the coating unit, and the neutralization step is performed by the above-described charging unit. The neutralizing means, the cleaning process can be suitably performed by the cleaning means, and the recycling process can be suitably performed by the recycling means.

<Electrostatic latent image forming step and electrostatic latent image forming means>
The electrostatic latent image forming step is a step of forming an electrostatic latent image on the electrophotographic photosensitive member.
The electrostatic latent image forming means is a means for forming an electrostatic latent image on the electrophotographic photosensitive member.

The electrostatic latent image can be formed, for example, by charging the surface of the electrophotographic photosensitive member and then exposing it like an image.
The electrostatic latent image forming unit includes, for example, at least a charger that charges the surface of the electrophotographic photosensitive member and an exposure device that exposes the surface of the electrophotographic photosensitive member imagewise.

The charging can be performed, for example, by applying a voltage to the surface of the electrophotographic photosensitive member using the charger.
The charger is not particularly limited and may be appropriately selected depending on the purpose. For example, a known contact charging device including a conductive or semiconductive roller, brush, film, rubber blade, etc. And non-contact chargers using corona discharge such as corotrons and corotrons.

The shape of the charging member may be any form such as a magnetic brush or a fur brush in addition to a roller, and can be selected according to the specifications and form of the electrophotographic forming apparatus. In the case of using a magnetic brush, the magnetic brush is composed of, for example, various ferrite particles such as Zn-Cu ferrite as a charging member, and a non-magnetic conductive sleeve for supporting the same, and a magnet roll included therein. . Or, when using a brush, for example, as a material of the fur brush, a fur treated with carbon, copper sulfide, metal or metal oxide is used, and this is wound or attached to a metal or other conductive core. To make a charger.
The charger is not limited to the contact charger as described above. However, since an image forming apparatus in which ozone generated from the charger is reduced is obtained, a contact charger is used. preferable.
It is preferable that the charger is arranged in contact or non-contact with the electrophotographic photosensitive member and charges the surface of the electrophotographic photosensitive member by applying DC and AC voltages in a superimposed manner.
Further, the charger is a charging roller that is disposed in close proximity to the electrophotographic photosensitive member via a gap tape, and charges the surface of the electrophotographic photosensitive member by applying a direct current and an alternating voltage to the charging roller. Those are preferred.

The exposure can be performed, for example, by exposing the surface of the electrophotographic photosensitive member imagewise using the exposure device.
The exposure device is not particularly limited as long as the surface of the electrophotographic photosensitive member charged by the charger can be exposed like an image to be formed, and can be appropriately selected according to the purpose. However, various exposure devices such as a copying optical system, a rod lens array system, a laser optical system, and a liquid crystal shutter optical system are exemplified.
Further, as the exposure, it is preferable to write a digital electrostatic latent image on the electrophotographic photosensitive member.
In the present invention, an optical backside system that performs imagewise exposure from the backside of the electrophotographic photosensitive member may be employed.

<Development process and development means>
The developing step is a step of developing the electrostatic latent image with toner or developer to form a toner image.
The developing means is means for developing the electrostatic latent image with toner or developer to form a toner image.
The toner is the toner described in the description of the electrophotographic overcoat composition of the present invention.
The developer is a developer using the toner.
The developing means is not particularly limited as long as it can be developed using, for example, the toner or the developer, and can be appropriately selected from known ones. For example, the toner or developer is accommodated. Preferred examples include those having at least a developing unit capable of bringing the toner or developer into contact or non-contact with the electrostatic latent image.

  The developing unit may be a dry developing type, a wet developing type, a single color developing unit, or a multi-color developing unit. For example, a toner having a stirrer for charging the toner or the developer by frictional stirring and a rotatable magnet roller is preferable.

  In the developing device, for example, the toner and the carrier are mixed and agitated, and the toner is charged by friction at that time, and held on the surface of the rotating magnet roller in a raised state to form a magnetic brush. . Since the magnet roller is disposed in the vicinity of the electrophotographic photosensitive member, a part of the toner constituting the magnetic brush formed on the surface of the magnet roller is electrically attracted to the electrophotographic photosensitive member. Move to the surface of the body. As a result, the electrostatic latent image is developed with the toner to form a toner image with the toner on the surface of the electrophotographic photosensitive member.

  The developer accommodated in the developing device may be a one-component developer or a two-component developer.

<Transfer process and transfer means>
The transfer step is a step of transferring the toner image to a recording medium.
The transfer unit is a unit that transfers the toner image to a recording medium.
For the transfer, an embodiment is preferred in which an intermediate recording medium is used, a toner image is primarily transferred onto the intermediate recording medium, and then the toner image is secondarily transferred onto the recording medium. Includes a primary transfer unit that uses a full-color toner to transfer a toner image onto an intermediate recording medium to form a composite transfer image, and a secondary transfer unit that transfers the composite transfer image onto a recording medium. Is more preferable.
The transfer can be performed, for example, by charging the toner image using a transfer charger, and can be performed by the transfer unit. The transfer unit includes a primary transfer unit that transfers a toner image onto an intermediate recording medium to form a composite transfer image, and a secondary transfer unit that transfers the composite transfer image onto a recording medium. Is preferred.
The intermediate recording medium is not particularly limited and may be appropriately selected from known recording media according to the purpose. For example, a transfer belt or the like is preferable.

The transfer unit (the primary transfer unit and the secondary transfer unit) preferably includes at least a transfer unit that peels and charges the toner image formed on the electrophotographic photosensitive member toward the recording medium. . There may be one transfer means or two or more transfer means.
Examples of the transfer device include a corona transfer device using corona discharge, a transfer belt, a transfer roller, a pressure transfer roller, and an adhesive transfer device.
The recording medium is the recording medium described in the description of the electrophotographic overcoat composition of the present invention.

<Application process and application means>
The coating step is a step of applying an electrophotographic overcoat composition to the toner image on the transferred recording medium.
The applying means is means for applying an electrophotographic overcoat composition to the transferred toner image on the recording medium.
The electrophotographic overcoat composition is the electrophotographic overcoat composition of the present invention.

  The electrophotographic overcoat composition is applied to the toner image on the recording medium at any suitable time in the fixing step or after the fixing step. For example, the electrophotographic overcoat composition may be performed immediately after the image is formed or in a printing apparatus with different printing and overcoating, such as inline coating in which printing and overcoating are performed on the same printing device. Like off-line coating, it is applied to the recording medium after a short or long delay time after printing.

  In the coating step, the electrophotographic overcoat composition is applied to the entire recording medium or the entire toner image as long as it is at least part of the toner image formed on the recording medium. It is not necessary, and can be appropriately selected according to the purpose such as protection of the printing surface and glossing.

  The application means is not particularly limited and can be appropriately selected depending on the purpose. For example, a roll coater, a flexo coater, a rod coater, a blade, a wire bar, an air knife, a curtain coater, a slide coater, a doctor knife, a screen. Examples of the liquid film coating apparatus include a coater, a gravure coater (for example, an offset gravure coater), a slot coater, an extrusion coater, and an inkjet coater. Such an apparatus can be used in a well-known manner such as forward and reverse roll coating, offset gravure, curtain coating, lithographic coating, screen coating, gravure coating, inkjet coating, and the like.

  There is no restriction | limiting in particular as average coating thickness of the said overcoat composition for electrophotography, Although it can select suitably according to the objective, 1 micrometer-15 micrometers are preferable. When the average coating thickness is less than 1 μm, repelling or gloss may be insufficient, and when it exceeds 15 μm, the texture of the image may be deteriorated.

After the coating step, it is preferable to cure the applied electrophotographic overcoat composition.
When the overcoat composition for electrophotography is a photocurable overcoat composition for electrophotography, it can be cured by irradiating light (mainly ultraviolet rays) from a light source.
When the electrophotographic overcoat composition is an oily electrophotographic overcoat composition, it can be cured by heating.

  The light source is not particularly limited and can be appropriately selected according to the purpose. For example, a low pressure mercury lamp, a medium pressure mercury lamp, a high pressure mercury lamp, an ultrahigh pressure mercury lamp, a xenon lamp, a carbon arc lamp, a metal halide lamp, a fluorescent lamp, Tungsten lamp, argon ion laser, helium cadmium laser, helium neon laser, krypton ion laser, various semiconductor lasers, YAG laser, light emitting diode, CRT light source, plasma light source, electron beam, gamma ray, ArF excimer laser, KrF excimer laser, F2 A laser etc. are mentioned.

FIG. 3 shows an example of the application means. The coating unit in FIG. 3 includes a coating roller 2, a metal roller 3, a press roller 5, a conveyor belt 6, a tray 7, a light source 8, and a scraper 9. The electrophotographic overcoat composition 1 is stored between the application roller 2 and the metal roller 3. The recording medium 4 on which the toner image is formed passes between the application roller 2 and the pressure roller 5 while being in contact with the rotating application roller 2 and the pressure roller 5. At that time, the electrophotographic overcoat composition 1 on the surface of the application roller 2 is transferred to the recording medium 4, whereby the electrophotographic overcoat composition 1 is applied to the recording medium 4.
The recording medium 4 coated with the electrophotographic overcoat composition 1 is transported by the transport belt 6 and passes under the light source 8. At that time, the electrophotographic overcoat composition 1 applied to the recording medium 4 is cured by ultraviolet rays from the light source 8. Thereafter, the recording medium 4 moves onto the tray 7.
The unnecessary electrophotographic overcoat composition 1 adhering to the pressure roller 5 is removed by the scraper 9.

<Other processes and other means>
-Fixing process and fixing means-
The fixing step is a step of fixing the toner image transferred to the recording medium using a fixing device.
The fixing means is means for fixing the toner image transferred to the recording medium using a fixing device.
The fixing may be performed each time the toner of each color is transferred to the recording medium, or may be performed at the same time in a state where the toner of each color is stacked.
There is no restriction | limiting in particular as said fixing device, Although it can select suitably according to the objective, A well-known heating-pressing means is suitable. Examples of the heating and pressing means include a combination of a heating roller and a pressing roller, a combination of a heating roller, a pressing roller, and an endless belt.
The heating in the heating and pressing means is usually preferably 80 ° C to 200 ° C.
In the present invention, for example, a known optical fixing device may be used together with or in place of the fixing step and the fixing unit depending on the purpose.

-Static elimination process and static elimination means-
The neutralization step is a step of performing neutralization by applying a neutralization bias to the electrophotographic photosensitive member.
Further, the static elimination means is a means for performing static elimination by applying an upper bias to the electrophotographic photosensitive member.
The neutralizing means is not particularly limited and may be appropriately selected from known neutralizers as long as it can apply a neutralizing bias to the electrophotographic photosensitive member. For example, a neutralizing lamp is preferably used. Can be mentioned.

-Cleaning process and cleaning means-
The cleaning step is a step of removing the toner remaining on the electrophotographic photosensitive member.
The cleaning means is means for removing the toner remaining on the electrophotographic photosensitive member.
The cleaning means is not particularly limited as long as it can remove the electrophotographic toner remaining on the electrophotographic photosensitive member, and can be appropriately selected from known cleaners. For example, a magnetic brush cleaner Suitable examples include electrostatic brush cleaners, magnetic roller cleaners, blade cleaners, brush cleaners, web cleaners, and the like.

-Recycling process and recycling means-
The recycling step is a step of recycling the toner removed by the cleaning step to the developing unit. The recycling unit is a unit of recycling the toner removed by the cleaning unit to the developing unit.
There is no restriction | limiting in particular as said recycling means, A well-known conveyance means etc. are mentioned.

-Control process and control means-
The said control process is a process of controlling each said process.
The control means is means for controlling the means.
The control means is not particularly limited as long as the movement of each means can be controlled, and can be appropriately selected according to the purpose. Examples thereof include devices such as sequencers and computers.

FIG. 4 shows an example of the image forming apparatus of the present invention. The image forming apparatus 100A includes a photosensitive drum 10, a charging roller 20 as a charging unit, an exposure device (not shown) as an exposure unit, and a developing unit (a black developing unit 45K and a yellow developing unit) as a developing unit. 45Y, magenta developing device 45M, cyan developing device 45C), intermediate transfer member 50, cleaning device 60 having a cleaning blade as a cleaning means, and static elimination lamp 70 as a static elimination means.
The intermediate transfer member 50 is an endless belt, is stretched by three rollers 51 arranged on the inner side thereof, and can move in the arrow direction. A part of the three rollers 51 also functions as a transfer bias roller that can apply a predetermined transfer bias (primary transfer bias) to the intermediate transfer member 50.
Further, a cleaning device 90 having a cleaning blade is disposed in the vicinity of the intermediate transfer member 50. Further, a transfer roller 80 as a transfer unit capable of applying a transfer bias for transferring (secondary transfer) the toner image to the recording medium 95 is disposed to face the intermediate transfer member 50.
Further, around the intermediate transfer member 50, a corona charger 52 for applying a charge to the toner image on the intermediate transfer member 50, a contact portion between the photosensitive drum 10 and the intermediate transfer member 50, and the intermediate transfer member 50 are provided. And the contact portion of the recording medium 95.
Black (K), yellow (Y), magenta (M), and cyan (C) developer units (black developer unit 45K, yellow developer unit 45Y, magenta developer unit 45M, cyan developer unit 45C) , A developer container (42K, 42Y, 42M, 42C), a developer supply roller (43K, 43Y, 43M, 43C), and a developing roller (44K, 44Y, 44M, 44C).
In the image forming apparatus 100A, the photosensitive drum 10 is uniformly charged by the charging roller 20, and then the exposure light 30 is exposed imagewise on the photosensitive drum 10 by an exposure device (not shown) to form an electrostatic latent image. Form. Next, a developer is supplied to the electrostatic latent image formed on the photosensitive drum 10 from a developing device (black developing device 45K, yellow developing device 45Y, magenta developing device 45M, cyan developing device 45C). Then, after developing and forming a toner image, the toner image is transferred (primary transfer) onto the intermediate transfer member 50 by the transfer bias applied from the roller 51. Further, the toner image on the intermediate transfer member 50 is given a charge by the corona charger 52 and then transferred (secondary transfer) onto the recording medium 95. The toner remaining on the photosensitive drum 10 is removed by the cleaning device 60, and the photosensitive drum 10 is once discharged by the discharging lamp 70.
In the image forming apparatus 100A, the application unit (not shown) can be disposed at an arbitrary position.

FIG. 5 shows another example of the image forming apparatus of the present invention. The image forming apparatus 100B is a tandem color image forming apparatus, and includes a copying apparatus main body 150, a paper feed table 200, a scanner 300, and an automatic document feeder (ADF) 400.
The copying apparatus main body 150 is provided with an endless belt-like intermediate transfer member 50 at the center. The intermediate transfer member 50 is stretched around the support rollers 14, 15 and 16, and can rotate in the direction of the arrow.

  A cleaning device 17 for removing the toner remaining on the intermediate transfer member 50 is disposed in the vicinity of the support roller 15. Further, four image forming units 18 of yellow, cyan, magenta, and black are arranged to face each other on the intermediate transfer member 50 stretched between the support roller 14 and the support roller 15 along the conveyance direction. A tandem developing device 120 is disposed. As shown in FIG. 6, the image forming means 18 for each color includes a photosensitive drum 10, a charging roller 20 that uniformly charges the photosensitive drum 10, and a black electrostatic latent image formed on the photosensitive drum 10. (K), yellow (Y), magenta (M), and cyan (C) are developed with each color developer to form a toner image, and each color toner image is transferred onto the intermediate transfer member 50. A transfer roller 62, a cleaning device 63, and a static elimination lamp 64.

An exposure device 21 is disposed in the vicinity of the tandem developing device 120. The exposure device 21 exposes the exposure light L on the photoconductor drum 10 (black photoconductor 10K, yellow photoconductor 10Y, magenta photoconductor 10M, cyan photoconductor 10C) to form an electrostatic latent image. .
Further, a secondary transfer device 22 is disposed on the side of the intermediate transfer member 50 opposite to the side on which the tandem developing device 120 is disposed. The secondary transfer device 22 includes a secondary transfer belt 24 that is an endless belt stretched between a pair of rollers 23, and the recording paper conveyed on the secondary transfer belt 24 and the intermediate transfer member 50 can contact each other. It has become.
A fixing device 25 is disposed in the vicinity of the secondary transfer device 22. The fixing device 25 includes a fixing belt 26 that is an endless belt, and a pressure roller 27 that is arranged to be pressed against the fixing belt 26.

Further, in the vicinity of the secondary transfer device 22 and the fixing device 25, a reversing device 28 for reversing the recording paper in order to form images on both sides of the recording paper is disposed.
Next, full color image formation (color copy) in the image forming apparatus 100B will be described. First, a document is set on the document table 130 of the automatic document feeder (ADF) 400, or the automatic document feeder 400 is opened and a document is set on the contact glass 32 of the scanner 300. close up. Next, when a start switch (not shown) is pressed, when the document is set on the automatic document feeder 400, the document is transported and moved onto the contact glass 32, and then the document is placed on the contact glass 32. When set, the scanner 300 is immediately driven, and the first traveling body 33 and the second traveling body 34 travel. At this time, light from the light source is emitted from the first traveling body 33, and reflected light from the document surface is reflected by a mirror in the second traveling body 34 and received by the reading sensor 36 through the imaging lens 35. . Thus, a color original (color image) is read, and image information of each color of black, yellow, magenta, and cyan is obtained.

  Further, after an electrostatic latent image of each color is formed on the photosensitive drum 10 based on the obtained image information of each color by the exposure device 21, the electrostatic latent image of each color is supplied from the developing device 61 of each color. The developed developer is used to form a toner image of each color. The formed toner images of the respective colors are sequentially transferred (primary transfer) on the intermediate transfer member 50 that is rotated and moved by the support rollers 14, 15, and 16, thereby forming a composite toner image on the intermediate transfer member 50. .

  In the paper feed table 200, one of the paper feed rollers 142 is selectively rotated to feed the recording paper from one of the paper feed cassettes 144 provided in multiple stages in the paper bank 143 and separated one by one by the separation roller 145. Then, the sheet is fed to the sheet feeding path 146, conveyed by the conveying roller 147, guided to the sheet feeding path 148 in the copying machine main body 150, and abutted against the registration roller 49 and stopped. Alternatively, the recording paper on the manual feed tray 151 is fed out, separated one by one by the separation roller 58, put into the manual feed path 53, and abutted against the registration roller 49 and stopped. The registration roller 49 is generally used while being grounded, but may be used in a state where a bias is applied to remove paper dust from the recording paper.

Then, the registration roller 49 is rotated in synchronization with the composite toner image formed on the intermediate transfer member 50, and the recording paper is sent between the intermediate transfer member 50 and the secondary transfer device 22, so that the composite toner image is transferred onto the recording paper. Transfer to (secondary transfer).
The recording sheet on which the composite toner image has been transferred is conveyed by the secondary transfer device 22 and sent out to the fixing device 25. In the fixing device 25, the composite toner image is fixed on the recording paper by being heated and pressed by the fixing belt 26 and the pressure roller 27. Thereafter, the recording paper is switched by the switching claw 55 and discharged by the discharge roller 56 and is stacked on the paper discharge tray 57. Alternatively, it is switched by the switching claw 55, reversed by the reversing device 28, guided again to the transfer position, formed on the back surface, discharged by the discharge roller 56, and stacked on the discharge tray 57.
The toner remaining on the intermediate transfer member 50 after the composite toner image is transferred is removed by the cleaning device 17.
In the image forming apparatus 100B, the application unit (not shown) can be disposed at an arbitrary position.

  Examples of the present invention will be described below, but the present invention is not limited to the following examples. In the examples, the mass% and the average molecular weight of the isoparaffin in the wax according to the present invention were measured by the FD (Field Deposition) method using JMS-T100GC “AccuTOF GC”.

Example 1
<Preparation of Toner 1 and Developer 1>
-Prescription-
Polyester resin 89 parts by mass (weight average molecular weight (MW): 68,200, glass transition temperature (Tg): 65.5 ° C.)
・ Microcrystalline wax 5 parts by mass-Isoparaffin 15% by mass
-Average molecular weight 650
Carbon black (Mitsubishi Kasei Co., Ltd., # 44) 5 parts by mass Charge control agent (Spiron Black TR-H, Hodogaya Chemical Co., Ltd.) 1 part by mass The above formulation is mixed and a biaxial extruder (BCTA type) After kneading at 120 ° C. using a Bühler company), pulverizing and classifying with an airflow type pulverizer (jet mill, manufactured by Nissin Engineering Co., Ltd.) to obtain a mass average particle diameter of 11.0 μm, a Henschel mixer (FM type, Toner 1 was obtained by mixing 2.2% by mass of silica (R-972: manufactured by Nippon Aerosil Co., Ltd.) using Mitsui Miike Chemical Co., Ltd.
The obtained toner had a toner average circularity of 0.90 and a volume average particle size of 8 μm.
As a carrier, magnetite particles having an average particle diameter of 50 μm coated with a silicone resin (thickness 0.5 μm) were used and mixed with the toner at a toner concentration of 5.0% by mass to obtain Developer 1.

<Preparation of overcoat composition 1>
30 parts by mass of pentaerythritol tetraacrylate, 66 parts by mass of trimethylolpropane triacrylate, and 0.3 parts by mass of hydroquinone as a polymerization inhibitor are placed in a beaker and heated to 120 ° C. with stirring. Further, a diallyl phthalate prepolymer (Daisodap 100, manufactured by Daiso Corporation) was dissolved. Further, 2 parts by mass of aluminum isopropylate dispersed in 2 parts by mass of toluene was gradually added and stirred at 110 ° C. for 20 minutes. During this time, toluene added as a solvent was removed from the system to obtain a desired photocurable varnish base agent.
Furthermore, 75 parts by mass of the photocurable varnish base agent, 50 parts by mass of acryloylmorpholine, 10 parts by mass of benzophenone as a photopolymerization initiator, 5 parts by mass of p-dimethylaminoacetophenone, and 10 parts by mass of phenyl glycol monoacrylate as a viscosity modifier. The mixture was mixed and sufficiently kneaded with a three-roll mill to obtain a photocurable overcoat composition 1.
It was 0.005 mass% when content of the organic solvent whose boiling point in the obtained photocurable overcoat composition 1 was 200 degrees C or less was measured with the following measuring method.

<Measurement>
-Content of organic solvent having a boiling point of 200 ° C or lower-
The content of the organic solvent having a boiling point of 200 ° C. or less in the overcoat composition 1 was determined by a measuring method according to the gas chromatographic method of JISK5601-5-1. The temperature was increased to 260 ° C. at a temperature increase rate of 10 ° C./min.

<Evaluation>
-Production of printed matter-
To Oji Paper Co. POD gloss coat as a recording medium (128g / ^{m 2),} an electrophotographic image under a condition of solid portion coating weight 0.4 mg / cm ² in imagio MP C7500 manufactured by Ricoh Company, Ltd. using developer 1 Was output to obtain a printed matter.

-Evaluation of repellency (wetting)-
Using a UV varnish coater (SG610V) manufactured by Shinano Kenshi Co., Ltd., coating the overcoat composition with an average coating thickness of 5 g / m ² (4.5 μm) on the printed surface of the printed matter at a coater speed of 10 m / min and an irradiation amount of 120 W / cm. went. The photocurable overcoat composition was cured with the above coater. The oily overcoat composition was dried and cured in a chamber without a lamp. The repellency of the overcoat composition of the printed matter after curing was visually evaluated according to the following evaluation criteria. The results are shown in Table 1-1.
◎: No repelling ○: Slightly repelled but no problem △: Repelled and problematical level ×: Remarkably repelled

-Adhesion evaluation-
Using a UV varnish coater (SG610V) manufactured by Shinano Kenshi, the overcoat composition was coated at a coater speed of 10 m / min and an irradiation amount of 120 W / cm with a thickness of 5 g / m ² (4.5 μm) on the printed surface. . The photocurable overcoat composition was cured with the above coater. Water and oily overcoat compositions were dried and cured in a chamber without a lamp.
The overcoat composition on the toner of the printed product after curing is cut with a cutter knife into a 100 square base pattern at intervals of 1 mm according to JIS K5400, peeled off with a cellophane adhesive tape, and the square that was not peeled off while being viewed with a loupe is counted. And evaluated according to the following evaluation criteria. The results are shown in Table 1-1.
A: 100/100
○: 80/100 to 99/100
Δ: 40/100 to 79/100
X: 0/100 to 39/100

(Example 2)
<Preparation of Toner 2 and Developer 2>
In Example 1, except that the microcrystalline wax was replaced with a mixed wax of microcrystalline wax and paraffin wax (isoparaffin 8 mass%, average molecular weight 520), toner 2 and developer 2 were prepared in the same manner as in Example 1. Obtained.
The obtained toner had a toner average circularity of 0.90 and a volume average particle size of 7 μm.

<Preparation of overcoat composition 2>
40 parts by mass of a polyester acrylate oligomer (EBECRYL846, manufactured by Daicel Cytec Co., Ltd., Mw1,100), 30 parts by mass of tripropylene glycol diacrylate, 90 parts by mass of acryloylmorpholine, 0.2 parts by mass of hydroquinone monomethyl ether as a polymerization inhibitor, photopolymerization start 8 parts by mass of benzoin ethyl ether as an agent and 3 parts by mass of triisopropanolamine as a sensitizer were mixed and stirred at 60 ° C. for 20 minutes to obtain a photocurable overcoat composition 2.
It was 0.007 mass% when content of the organic solvent whose boiling point in the obtained photocurable overcoat composition 2 was 200 degrees C or less was measured by the said measuring method.

<Evaluation>
In Example 1, evaluation was performed in the same manner as in Example 1 except that the developer and the overcoat composition were replaced with the developer 2 and the overcoat composition 2 obtained above. The results are shown in Table 1-1.

(Example 3)
<Preparation of Toner 3 and Developer 3>
In Example 1, a toner 3 and a developer 3 are obtained in the same manner as in Example 1 except that the microcrystalline wax is replaced with a mixed wax of microcrystalline wax and paraffin wax (isoparaffin 11 mass%, average molecular weight 470). It was.
The obtained toner had a toner average circularity of 0.91 and a volume average particle size of 7.8 μm.

<Preparation of overcoat composition 3>
40 parts by mass of urethane acrylate oligomer (EBECRYL5129, manufactured by Daicel Cytec Co., Ltd., Mw800), 40 parts by mass of hexanediol diacrylate, 10 parts by mass of cyclohexyl acrylate, 5 parts by mass of methacryloylmorpholine, 0.2 part by mass of hydroquinone monomethyl ether as a polymerization inhibitor, And 6 parts by mass of benzyl (1,2-diphenylethanedione) as a photopolymerization initiator was mixed and stirred at 60 ° C. for 20 minutes to obtain a photocurable overcoat composition 3.
It was 0.006 mass% when content of the organic solvent whose boiling point in the obtained photocurable overcoat composition 3 was 200 degrees C or less was measured by the said measuring method.

<Evaluation>
In Example 1, evaluation was performed in the same manner as in Example 1 except that the developer and the overcoat composition were replaced with the developer 3 and the overcoat composition 3 obtained above. The results are shown in Table 1-1.

Example 4
<Preparation of Overcoat Composition 4>
60 parts by mass of a polyester acrylate oligomer (EBECRYL 1830, manufactured by Daicel Cytec Co., Ltd., Mw 1,500), 30 parts by mass of bisphenol A ethylene oxide adduct diacrylate (V # 700, manufactured by Osaka Organic Chemical Co., Ltd.), 5 parts by mass of 2-ethylhexyl acrylate, 20 parts by mass of methacryloylmorpholine, 0.4 parts by mass of 2,6-ditert-butyl-p-cresol (BHT) as a polymerization inhibitor, and 9 parts by mass of Irgacure 184 (manufactured by Ciba Specialty Chemicals) as a photopolymerization initiator Were mixed and stirred at 60 ° C. for 20 minutes to obtain a photocurable overcoat composition 4.
It was 0.004 mass% when content of the organic solvent whose boiling point in the obtained photocurable overcoat composition 4 was 200 degrees C or less was measured by the said measuring method.

<Evaluation>
Evaluation was performed in the same manner as in Example 1 except that the overcoat composition 4 was replaced with the overcoat composition 4 in Example 1. The results are shown in Table 1-1.

(Example 5)
<Preparation of overcoat composition 5>
Calton Self GW Varnish (manufactured by DIC) was used. The varnish is composed of rosin-modified phenolic resin varnish, polymerized linseed oil, light oil, and auxiliary agents (dryers, film reinforcing agents, etc.). The overcoat composition 5 was obtained by mixing 100 parts by weight of Carton Self GW varnish and 15 parts by weight of methacryloylmorpholine and stirring at 30 ° C. for 10 minutes.
It was 0.005 mass% when content of the organic solvent whose boiling point in the obtained photocurable overcoat composition 5 was 200 degrees C or less was measured by the said measuring method.

<Evaluation>
Evaluation was performed in the same manner as in Example 1 except that the overcoat composition 5 was replaced with the overcoat composition 5 in Example 1. The results are shown in Table 1-1.

(Example 6)
<Preparation of overcoat composition 6>
In Example 1, except that the photocurable varnish base agent was changed from 75 parts by mass to 70 parts by mass and 5 parts by mass of polyoxyethylene glycol alkyl ether as a surfactant was blended, A photocurable overcoat composition 6 was obtained.
It was 0.006 mass% when content of the organic solvent whose boiling point in the obtained photocurable overcoat composition 6 was 200 degrees C or less was measured by the said measuring method.

<Evaluation>
Evaluation was performed in the same manner as in Example 1 except that the overcoat composition 6 was replaced with the overcoat composition 6 in Example 1. The results are shown in Table 1-1.

(Example 7)
<Preparation of overcoat composition 7>
In Example 4, the amount of 2-ethylhexyl acrylate was changed from 5 parts by mass to 3 parts by mass, and 2 parts by mass of sodium dialkylsulfosuccinate (anionic surfactant) was added. A coating composition 7 was obtained.
It was 0.004 mass% when content of the organic solvent whose boiling point in the obtained photocurable overcoat composition 7 was 200 degrees C or less was measured by the said measuring method.

<Evaluation>
Evaluation was performed in the same manner as in Example 1 except that the overcoat composition was replaced with the overcoat composition 7 in Example 1. The results are shown in Table 1-1.

(Example 8)
<Preparation of overcoat composition 8>
In Example 5, the amount of overload was changed in the same manner as in Example 5 except that the calton self GW varnish was changed from 100 parts by mass to 96 parts by mass and 4 parts by mass of alkylbenzene sulfonate (anionic surfactant) was added. A coating composition 8 was obtained.
It was 0.005 mass% when content of the organic solvent whose boiling point in the obtained photocurable overcoat composition 8 was 200 degrees C or less was measured by the said measuring method.

<Evaluation>
Evaluation was performed in the same manner as in Example 1 except that the overcoat composition was replaced with the overcoat composition 8 in Example 1. The results are shown in Table 1-1.

Example 9
<Manufacture of toner 4 and developer 4>
<< Production of Toner 4 >>
-Dissolution of toner material or preparation of dispersion-
--- Synthesis of unmodified polyester (low molecular weight polyester)-
In a reaction vessel equipped with a cooling tube, a stirrer and a nitrogen introduction tube, 67 parts by mass of bisphenol A ethylene oxide 2 mol adduct, 84 parts by mass of bisphenol A propion oxide 3 mol adduct, 274 parts by mass of terephthalic acid, and dibutyltin oxide 2 parts by mass were added and reacted at 230 ° C. under normal pressure for 8 hours.
Subsequently, the obtained reaction liquid was reacted under reduced pressure of 10 mmHg to 15 mmHg for 5 hours to synthesize an unmodified polyester.
The obtained unmodified polyester had a number average molecular weight (Mn) of 2,100, a weight average molecular weight (Mw) of 5,600, and a glass transition temperature (Tg) of 55 ° C.

-Preparation of master batch (MB)-
1,000 parts by weight of water, 540 parts by weight of carbon black (Printex 35, manufactured by Degussa, DBP oil absorption = 42 mL / 100 g, pH = 9.5) and 1,200 parts by weight of the unmodified polyester were mixed with a Henschel mixer ( (Mitsui Mining Co., Ltd.).
The obtained mixture was kneaded with a two roll at 150 ° C. for 30 minutes, then rolled and cooled, and pulverized with a pulverizer (manufactured by Hosokawa Micron Corporation) to prepare a master batch.

--Synthesis of prepolymer--
In a reaction vessel equipped with a cooling tube, a stirrer and a nitrogen introduction tube, 682 parts by mass of bisphenol A ethylene oxide 2 mol adduct, 81 parts by mass of bisphenol A propylene oxide 2 mol adduct, 283 parts by mass of terephthalic acid, trimellitic anhydride 22 parts by mass of acid and 2 parts by mass of dibutyltin oxide were charged and reacted at 230 ° C. for 8 hours under normal pressure.
Subsequently, it was made to react under reduced pressure of 10 mmHg-15 mmHg for 5 hours, and the intermediate polyester was synthesize | combined.
The obtained intermediate polyester has a number average molecular weight (Mn) of 2,100, a weight average molecular weight (Mw) of 9,600, a glass transition temperature (Tg) of 55 ° C., an acid value of 0.5, and a hydroxyl value of 49.
Next, 411 parts by mass of the intermediate polyester, 89 parts by mass of isophorone diisocyanate, and 500 parts by mass of ethyl acetate are charged in a reaction vessel equipped with a cooling tube, a stirrer, and a nitrogen introduction tube, and reacted at 100 ° C. for 5 hours. Thus, a prepolymer (modified polyester capable of reacting with an active hydrogen group-containing compound) was synthesized.
The free isocyanate content of the obtained prepolymer was 1.60% by mass, and the solid content concentration of the prepolymer (after standing at 150 ° C. for 45 minutes) was 50% by mass.

--Synthesis of ketimine (the active hydrogen group-containing compound)-
In a reaction vessel equipped with a stirrer and a thermometer, 30 parts by mass of isophoronediamine and 70 parts by mass of methyl ethyl ketone were charged and reacted at 50 ° C. for 5 hours to synthesize a ketimine compound (active hydrogen group-containing compound).
The amine value of the obtained ketimine compound (the active hydrogen machine-containing compound) was 423.

--Synthesis of styrene-acrylic copolymer resin--
In a reaction vessel equipped with a cooling pipe, a stirrer and a nitrogen introduction pipe, 300 parts by mass of ethyl acetate was charged, and a styrene-acrylic monomer mixture (styrene / 2-ethylhexyl acrylate / acrylic acid / 2-hydroxylethyl acrylate = 75 / 15/5/5) 300 parts by mass and 10 parts by mass of azobisisobutylnitrile were added and reacted at 60 ° C. for 15 hours in a normal pressure nitrogen atmosphere.
Next, 200 parts by mass of methanol was added to the reaction solution, and after stirring for 1 hour, the supernatant was removed and dried under reduced pressure to synthesize a styrene-acrylic copolymer resin.

--Dissolution of toner material or preparation of dispersion liquid--
In a beaker, 10 parts by mass of the prepolymer, 60 parts by mass of the unmodified polyester, 130 parts by mass of ethyl acetate, and 30 parts by mass of the styrene-acrylic copolymer were stirred and dissolved.
Next, 10 parts by mass of microcrystalline wax (isoparaffin 15% by mass, average molecular weight = 650) and 10 parts by mass of the master batch were charged, and using a bead mill (Ultra Visco Mill, manufactured by Imex Corporation), a liquid feeding speed of 1 kg / hr. Then, a raw material solution is prepared by three passes under conditions where the disk peripheral speed is 6 m / s and 80% by volume of 0.5 mm zirconia beads are filled. A dispersion was prepared.

-Preparation of aqueous medium phase-
An aqueous medium phase was prepared by mixing and stirring 306 parts by mass of ion-exchanged water, 265 parts by mass of a 10% by mass tricalcium phosphate suspension, and 0.2 parts by mass of sodium dodecylbenzenesulfonate, and dissolving them uniformly.

-Preparation of emulsion or dispersion-
150 parts by mass of the aqueous medium phase is placed in a container, and stirred at a rotational speed of 12,000 rpm using a TK homomixer (manufactured by Tokushu Kika Kogyo Co., Ltd.). The mixture was added and mixed for 10 minutes to prepare an emulsified dispersion (emulsified slurry).

-Removal of organic solvent-
100 parts by mass of the emulsified slurry was charged in a Kolben equipped with a stirrer and a thermometer, and the solvent was removed at 30 ° C. for 12 hours while stirring at a stirring peripheral speed of 20 m / min to obtain a dispersed slurry.

-Cleaning and drying-
After 100 parts by mass of the dispersion slurry was filtered under reduced pressure, 100 parts by mass of ion-exchanged water was added to the filter cake, mixed with a TK homomixer (10 minutes at a rotational speed of 12,000 rpm), and then filtered.
To the obtained filter cake, 300 parts by mass of ion-exchanged water was added, mixed with a TK homomixer (10 minutes at 12,000 rpm), and then filtered twice.
To the obtained filter cake, 20 parts by mass of a 10% by mass aqueous sodium hydroxide solution was added, mixed with a TK homomixer (30 minutes at 12,000 rpm), and then filtered under reduced pressure.
To the obtained filter cake, 300 parts by mass of ion-exchanged water was added, mixed with a TK homomixer (at 12,000 rpm for 10 minutes), and then filtered.
To the obtained filter cake, 300 parts by mass of ion-exchanged water was added, mixed with a TK homomixer (10 minutes at 12,000 rpm), and then filtered twice.
Furthermore, 20 mass parts of 10 mass% hydrochloric acid was added to the obtained filter cake, mixed with a TK homomixer (at a rotation speed of 12,000 rpm for 10 minutes) and then filtered.
To the obtained filter cake, 300 parts by mass of ion-exchanged water was added, mixed with a TK homomixer (10 minutes at a rotation speed of 12,000 rpm), and then filtered twice to obtain a final filter cake.
The obtained final filter cake was dried with a circulating dryer at 45 ° C. for 48 hours, and sieved with an opening of 75 μm mesh to obtain toner base particles.

-External treatment-
With respect to 100 parts by mass of the obtained toner base particles, 0.6 part by mass of hydrophobic silica having a volume average particle diameter of 100 nm, 1.0 part by mass of titanium oxide having a volume average particle diameter of 20 nm, and a volume average particle diameter of 15 nm. Toner 4 was obtained by mixing 0.8 parts by mass of hydrophobic silica fine powder with a Henschel mixer.
The obtained toner had an average circularity of 0.940 and a volume average particle size of 5.7 μm.

<< Manufacture of Developer 4 >>
-Carrier manufacturing-
Acrylic resin solution (cyclohexyl methacrylate / methyl methacrylate = 80/20 (mass ratio) toluene solution of copolymer (Mw: 55,000), synthesis from monomers manufactured by Mitsubishi Rayon Co., Ltd., solid content 50 mass%) 21.0 mass Parts, guanamine solution (Super Becamine TD-126, manufactured by DIC, solid content 70% by mass), 6.4 parts by mass, alumina particles (Sumicorundum AA-03, manufactured by Sumitomo Chemical Co., Ltd., particle size 0.3 μm, specific resistance) Value 10 ¹⁴ (Ω · cm)) 7.6 parts by mass, silicon resin solution 65.0 parts by mass (SR2410, manufactured by Toray Dow Corning Silicone Co., Ltd., solid content 23% by mass), aminosilane (SH6020, Toray Dow Corning)・ Silicon Co., Ltd. (solid content: 100% by mass) 1.0 part by mass, toluene: 60 parts by mass, and butyl cellosolve: 60 parts by mass They were dispersed for 10 minutes by a homomixer to obtain a coating film forming solution of acrylic resin and silicone resin containing alumina particles.
A fired ferrite powder [(MgO) 1.8 (MnO) 49.5 (Fe ₂ O ₃ ) 48.0: average particle size 35 μm] was used as the core material, and the above coating film forming solution had a thickness of 0 on the surface of the core material. After coating with a Spira coater (Okada Seiko Co., Ltd.) to a thickness of 15 μm and drying, the product was left standing in an electric furnace at 150 ° C. for 1 hour and baked. After cooling, the mixture was crushed using a sieve having an aperture of 106 μm to obtain a carrier having a weight average particle diameter of 35 μm.

-Production of developer-
The developer 4 was obtained by uniformly mixing and charging 7 parts by mass of the toner with respect to 100 parts by mass of the carrier using a tumbler mixer of a type in which the container rolls and stirs.

<Evaluation>
In Example 1, the evaluation was performed in the same manner as in Example 1 except that the developer was replaced with the developer 4 obtained above. The results are shown in Table 1-1.

(Example 10)
<Preparation of Toner 5 and Developer 5>
In Example 1, a toner 5 and a developer 5 are obtained in the same manner as in Example 1 except that the microcrystalline wax is replaced with a mixed wax of microcrystalline wax and paraffin wax (isoparaffin 8 mass%, average molecular weight 520). It was.
The obtained toner had a toner average circularity of 0.90 and a volume average particle size of 7.5 μm.

<Evaluation>
In Example 1, the evaluation was performed in the same manner as in Example 1 except that the developer was replaced with the developer 5 obtained above. The results are shown in Table 1-1.

(Example 11)
<Preparation of Toner 6 and Developer 6>
In Example 9, toner 6 and developer 6 are obtained in the same manner as in Example 9, except that the microcrystalline wax is replaced with a mixed wax of microcrystalline wax and paraffin wax (isoparaffin 11 mass%, average molecular weight 470). It was.
The obtained toner had a toner average circularity of 0.95 and a volume average particle size of 5.8 μm.

<Evaluation>
In Example 1, the evaluation was performed in the same manner as in Example 1 except that the developer was replaced with the developer 6 obtained above. The results are shown in Table 1-1.

(Example 12)
<Preparation of Toner 7 and Developer 7>
In Example 1, a toner 7 and a developer 7 were obtained in the same manner as in Example 1 except that the microcrystalline wax was replaced with paraffin wax (isoparaffin 2 mass%, average molecular weight 400).
The obtained toner had a toner average circularity of 0.90 and a volume average particle size of 7.6 μm.

<Evaluation>
In Example 1, evaluation was performed in the same manner as in Example 1 except that the developer and the overcoat composition were replaced with the developer 7 and the overcoat composition 2 obtained above. The results are shown in Table 1-1.

(Example 13)
<Preparation of Toner 8 and Developer 8>
In Example 9, a toner 8 and a developer 8 were obtained in the same manner as in Example 9 except that the microcrystalline wax was replaced with paraffin wax (isoparaffin 2 mass%, average molecular weight 400).
The obtained toner had a toner average circularity of 0.95 and a volume average particle size of 5.7 μm.

<Evaluation>
In Example 1, evaluation was performed in the same manner as in Example 1 except that the developer and the overcoat composition were replaced with the developer 8 and the overcoat composition 3 obtained above. The results are shown in Table 1-1.

(Example 14)
<Preparation of overcoat composition 9>
30 parts by mass of pentaerythritol tetraacrylate, 66 parts by mass of trimethylolpropane triacrylate, and 0.3 parts by mass of hydroquinone as a polymerization inhibitor are placed in a beaker and heated to 120 ° C. with stirring. Further, a diallyl phthalate prepolymer (Daisodap 100, manufactured by Daiso Corporation) was dissolved. Further, 2 parts by mass of aluminum isopropylate dispersed in 2 parts by mass of toluene was gradually added and stirred at 110 ° C. for 20 minutes. During this time, toluene added as a solvent was removed from the system to obtain a desired photocurable varnish base agent.
Furthermore, 75 parts by mass of the photocurable varnish base agent, 5.3 parts by mass of acryloylmorpholine, 10 parts by mass of benzophenone as a photopolymerization initiator, 5 parts by mass of p-dimethylaminoacetophenone, and 10 parts by mass of phenyl glycol monoacrylate as a viscosity modifier. The parts were mixed and sufficiently kneaded with a three-roll mill to obtain a photocurable overcoat composition 9.
It was 0.004 mass% when content of the organic solvent whose boiling point in the obtained photocurable overcoat composition 9 was 200 degrees C or less was measured by the said measuring method.

<Evaluation>
In Example 1, evaluation was performed in the same manner as in Example 1 except that the overcoat composition was replaced with the overcoat composition 9 obtained above. The results are shown in Table 1-1.

(Example 15)
<Preparation of Overcoat Composition 10>
30 parts by mass of pentaerythritol tetraacrylate, 66 parts by mass of trimethylolpropane triacrylate, and 0.3 parts by mass of hydroquinone as a polymerization inhibitor are placed in a beaker and heated to 120 ° C. with stirring. Further, a diallyl phthalate prepolymer (Daisodap 100, manufactured by Daiso Corporation) was dissolved. Further, 2 parts by mass of aluminum isopropylate dispersed in 2 parts by mass of toluene was gradually added and stirred at 110 ° C. for 20 minutes. During this time, toluene added as a solvent was removed from the system to obtain a desired photocurable varnish base agent.
Furthermore, 75 parts by mass of the photocurable varnish base agent, 42.9 parts by mass of acryloylmorpholine, 10 parts by mass of benzophenone as a photopolymerization initiator, 5 parts by mass of p-dimethylaminoacetophenone, and 10 parts by mass of phenyl glycol monoacrylate as a viscosity modifier. The parts were mixed and sufficiently kneaded with a three-roll mill to obtain a photocurable overcoat composition 10.
It was 0.006 mass% when content of the organic solvent whose boiling point in the obtained photocurable overcoat composition 10 was 200 degrees C or less was measured by the said measuring method.

<Evaluation>
In Example 1, the evaluation was performed in the same manner as in Example 1 except that the overcoat composition was replaced with the overcoat composition 10 obtained above. The results are shown in Table 1-1.

(Example 16)
In Example 1, evaluation was performed in the same manner as in Example 1 except that only a toner image portion was overcoated using a mask. Since the background portion was not overcoated, a glossy printed material was obtained only in the image portion. The results are shown in Table 1-1.

(Example 17)
<Preparation of Toner 9 and Developer 9>
In Example 1, a toner 9 and a developer 9 were obtained in the same manner as in Example 1 except that the polyester resin was replaced with St-Ar resin (FCA-207AP, manufactured by Fujikura Kasei Co., Ltd., Mw 22,000).
The obtained toner had a toner average circularity of 0.90 and a volume average particle size of 8 μm.

<Evaluation>
In Example 1, the evaluation was performed in the same manner as in Example 1 except that the developer was replaced with the developer 9 obtained above. The results are shown in Table 1-1.

(Comparative Example 1)
<Preparation of Overcoat Composition 1X>
An overcoat composition 1X was obtained in the same manner as in Example 1 except that acryloylmorpholine was replaced with 1,9-nonanediol diacrylate in Example 1.

<Evaluation>
In Example 1, the evaluation was performed in the same manner as in Example 1 except that the overcoat composition was replaced with the overcoat composition 1X. The results are shown in Table 1-2.

(Comparative Example 2)
<Preparation of Overcoat Composition 2X>
In Example 2, an overcoat composition 2X was obtained in the same manner as in Example 2 except that acryloylmorpholine was replaced with 1,9-nonanediol diacrylate.

<Evaluation>
In Example 2, the evaluation was performed in the same manner as in Example 2 except that the overcoat composition was replaced with the overcoat composition 2X. The results are shown in Table 1-2.

(Comparative Example 3)
<Preparation of overcoat composition 3X>
An overcoat composition 3X was obtained in the same manner as in Example 3 except that methacryloylmorpholine was replaced with 1,9-nonanediol diacrylate in Example 3.

<Evaluation>
In Example 3, the evaluation was performed in the same manner as in Example 3 except that the overcoat composition was replaced with the overcoat composition 3X. The results are shown in Table 1-2.

(Comparative Example 4)
<Preparation of Overcoat Composition 4X>
In Example 4, an overcoat composition 4X was obtained in the same manner as in Example 4 except that methacryloylmorpholine was replaced with 2-ethoxyethyl acrylate.

<Evaluation>
In Example 1, the evaluation was performed in the same manner as in Example 1 except that the overcoat composition was replaced with the overcoat composition 4X. The results are shown in Table 1-2.

(Comparative Example 5)
<Preparation of overcoat composition 5X>
An overcoat composition 5X was obtained in the same manner as in Example 5 except that in Example 5, methacryloylmorpholine was replaced with 2-ethoxyethyl acrylate.

<Evaluation>
Evaluation was performed in the same manner as in Example 1 except that the overcoat composition was replaced with the overcoat composition 5X in Example 1. The results are shown in Table 1-2.

(Comparative Example 6)
<Preparation of Overcoat Composition 6X>
An overcoat composition 6X was obtained in the same manner as in Example 6 except that acryloylmorpholine was replaced with 2-ethoxyethyl acrylate in Example 6.

<Evaluation>
In Example 1, evaluation was performed in the same manner as in Example 1 except that the overcoat composition was replaced with the overcoat composition 6X. The results are shown in Table 1-2.

(Comparative Example 7)
<Preparation of overcoat composition 7X>
An overcoat composition 7X was obtained in the same manner as in Example 7, except that in Example 7, methacryloylmorpholine was replaced with 2-methoxyethyl acrylate.

<Evaluation>
In Example 1, evaluation was performed in the same manner as in Example 1 except that the overcoat composition was replaced with the overcoat composition 7X. The results are shown in Table 1-2.

(Comparative Example 8)
<Preparation of Overcoat Composition 8X>
In Example 8, an overcoat composition 8X was obtained in the same manner as in Example 8 except that methacryloylmorpholine was replaced with 2-methoxyethyl acrylate.

<Evaluation>
Evaluation was performed in the same manner as in Example 1 except that the overcoat composition was replaced with the overcoat composition 8X in Example 1. The results are shown in Table 1-2.

(Comparative Example 9)
<Evaluation>
Evaluation was performed in the same manner as in Example 1 except that the developer and the overcoat composition were replaced with the developer 4 and the overcoat composition 1X in Example 1. The results are shown in Table 1-2.

(Comparative Example 10)
<Evaluation>
In Example 1, the evaluation was performed in the same manner as in Example 1 except that the developer and the overcoat composition were replaced with the developer 5 and the overcoat composition 1X. The results are shown in Table 1-2.

(Comparative Example 11)
<Evaluation>
Evaluation was performed in the same manner as in Example 1 except that the developer and the overcoat composition were replaced with the developer 6 and the overcoat composition 1X in Example 1. The results are shown in Table 1-2.

(Comparative Example 12)
<Evaluation>
Evaluation was performed in the same manner as in Example 1 except that the developer and the overcoat composition were replaced with the developer 7 and the overcoat composition 2X in Example 1. The results are shown in Table 1-2.

(Comparative Example 13)
<Evaluation>
In Example 1, evaluation was performed in the same manner as in Example 1 except that the developer and the overcoat composition were replaced with the developer 8 and the overcoat composition 3X. The results are shown in Table 1-2.

(Comparative Example 14)
<Preparation of overcoat composition 9X>
An overcoat composition 9X was obtained in the same manner as in Example 1 except that acryloylmorpholine was replaced with N, N-dimethylacrylamide in Example 1.

<Evaluation>
In Example 1, evaluation was performed in the same manner as in Example 1 except that the overcoat composition was replaced with the overcoat composition 9X. The results are shown in Table 1-2.

(Comparative Example 15)
<Preparation of Overcoat Composition 10X>
In Example 2, an overcoat composition 10X was obtained in the same manner as in Example 2, except that acryloylmorpholine was replaced with N, N-dimethylacrylamide.

<Evaluation>
In Example 2, the evaluation was performed in the same manner as in Example 2 except that the overcoat composition was replaced with the overcoat composition 10X. The results are shown in Table 1-2.

(Comparative Example 16)
<Preparation of Overcoat Composition 11X>
In Example 3, an overcoat composition 11X was obtained in the same manner as in Example 3 except that methacryloylmorpholine was replaced with N, N-dimethylacrylamide.

<Evaluation>
Evaluation was performed in the same manner as in Example 3 except that the overcoat composition was replaced with the overcoat composition 11X in Example 3. The results are shown in Table 1-2.

(Comparative Example 17)
<Evaluation>
In Example 1, the evaluation was performed in the same manner as in Example 1 except that the developer and the overcoat composition were replaced with the developer 9 and the overcoat composition 1X. The results are shown in Table 1-2.

  The electrophotographic overcoat composition of the present invention has excellent adhesion without repelling a toner image on a recording medium, for example, a toner image containing a wax. It is suitably used for electrophotographic image formation in which protection and gloss are imparted.

DESCRIPTION OF SYMBOLS 1 Electrophotographic overcoat composition 2 Application | coating roller 3 Metal roller 4 Recording medium 5 Pressure roller 6 Conveyor belt 7 Tray 8 Light source 9 Scraper 10 Photoconductor drum 10K Photoconductor for black 10Y Photoconductor for yellow 10M Photoconductor for magenta 10C Cyan Photoconductor 14, 15, 16 Support roller 17 Cleaning device 18 Image forming means 20 Charging roller 21 Exposure device 22 Secondary transfer device 23 Roller 24 Secondary transfer belt 25 Fixing device 26 Fixing belt 27 Pressure roller 28 Reversing device 30 Exposure Light 32 Contact glass 33 First traveling body 34 Second traveling body 35 Imaging lens 36 Reading sensor 42K, 42Y, 42M, 42C Developer accommodating portion 43K, 43Y, 43M, 43C Developer supply roller 44K, 44Y, 44M, 4C Development roller 45K Black development unit 45Y Yellow development unit 45M Magenta development unit 45C Cyan development unit 49 Registration roller 50 Intermediate transfer member 51 Roller 52 Corona charger 53 Manual paper feed path 55 Switching claw 56 Ejection roller 57 Ejection Tray 58 Separating roller 60 Cleaning device 61 Developing device 62 Transfer roller 63 Cleaning device 64 Static elimination lamp 70 Static elimination lamp 80 Transfer roller 90 Cleaning device 95 Recording medium 100A, 100B Image forming device 120 Tandem type developer 130 Document base 142 Feed roller 143 Paper bank 144 Paper feed cassette 145 Separation roller 146 Paper feed path 147 Transport roller 148 Paper feed path 150 Copier main body 151 Manual feed tray 200 Paper feed table 300 Scanner 400 Automatic document feeder L Exposure light

JP 2007-277547 A Japanese Patent Laid-Open No. 10-309876 Japanese Patent No. 2522333

Claims (11)

An overcoat composition for electrophotography used for overcoating a toner image prepared on a recording medium by an electrophotographic method using toner, comprising at least a compound represented by the following general formula (1) An overcoat composition for electrophotography characterized by the above.
In the general formula (1), R ¹ represents a hydrogen atom or a methyl group.   The overcoat composition for electrophotography according to claim 1, which contains substantially no organic solvent having a boiling point of 200 ° C or lower.   The electrocoat overcoat composition according to claim 1, wherein the content of the compound represented by the general formula (1) is 1% by mass to 50% by mass.   The overcoat composition for electrophotography according to any one of claims 1 to 3, further comprising a surfactant.   The overcoat composition for electrophotography according to any one of claims 1 to 4, which is a photocurable type. A charging step for charging the surface of the electrophotographic photosensitive member;
Exposing the charged surface of the electrophotographic photosensitive member imagewise to form an electrostatic latent image; and
Developing the electrostatic latent image with toner to form a toner image;
A transfer step of transferring the developed toner image to a recording medium;
An application step of applying an electrophotographic overcoat composition to the toner image on the transferred recording medium,
The electrophotographic overcoat composition according to any one of claims 1 to 5, wherein the electrophotographic overcoat composition is the electrophotographic overcoat composition.   The electrophotographic forming method according to claim 6, wherein the toner contains a wax.   The electrophotographic method according to any one of claims 6 to 7, wherein an average coating thickness of the overcoat composition is 1 µm to 15 µm. An electrophotographic photoreceptor;
Charging means for charging the surface of the electrophotographic photosensitive member;
Exposure means for imagewise exposing the surface of the charged electrophotographic photoreceptor to form an electrostatic latent image;
Developing means for developing the electrostatic latent image with toner to form a toner image;
Transfer means for transferring the developed toner image to a recording medium;
Application means for applying an electrophotographic overcoat composition to the toner image on the transferred recording medium,
The electrophotographic overcoat composition according to any one of claims 1 to 5, wherein the electrophotographic overcoat composition is an electrophotographic overcoat composition.   The electrophotographic apparatus according to claim 9, wherein the toner contains a wax.   The electrophotographic apparatus according to claim 9, which forms a color image.