JP5892749B2 - Toner production method - Google Patents

Description

  The present invention relates to a toner suitably used in an electrophotographic method, an electrostatic recording method, an electrostatic printing method, and the like, a manufacturing method thereof, a developer using the toner, a container containing toner, a process cartridge, a fixing method, and an image. The present invention relates to a forming apparatus and an image forming method.

As a fixing method used in the dry development method, a heat-heat roller method is widely used because of its energy efficiency.
In recent years, in order to save energy by fixing the toner at a low temperature, the thermal energy given to the toner during fixing tends to be small.
According to the 1999 International Energy Agency (IEA) Demand-side Management (DSM) program, the next generation copier is a copier with a copy speed (CPM) of 30 or more. Therefore, it is required to have a power consumption of 10 to 30 watts or less (different depending on the copying speed), and achieving energy saving is a very important issue.
As a means for achieving this, a method is considered in which the fixing temperature of the toner itself is lowered to lower the toner fixing temperature during use.
As a method for fixing the toner at a low temperature, for example, a method using a specific non-olefinic crystalline polymer having a sharp melt property at a low glass transition temperature or a crystalline polyester in a binder resin has been proposed. .
However, the resin having such crystallinity may not be able to achieve low-temperature fixing of the toner depending on the combination with other resins forming the toner.
Further, even if the crystalline resin is used only, the toner can be fixed at a low temperature, but there is a problem that a hot offset phenomenon or a blocking phenomenon occurs.

For example, Japanese Patent Application Laid-Open No. 2002-108018 of Patent Document 1 improves the low-temperature fixability of toner by including a binder resin containing a crystalline resin having at least one melting point (particularly a crystalline polyester resin). The toner is described.
Japanese Patent Application Laid-Open No. 2002-214831 of Patent Document 2 discloses an image forming method in which low-temperature fixability of toner is improved by using a toner containing a crystalline polyester resin as a main component as a binder resin. Have been described.
However, these toners use a crystalline polyester resin as a binder resin as a main component, and therefore, when melt-kneaded, cause the above-mentioned problems due to nonuniformity of the colorant and release agent in the toner. There is.

Further, for example, Japanese Patent Application Laid-Open No. 2003-167384 of Patent Document 3 describes a toner that contains a crystalline resin and an amorphous resin as binder resins, and these are incompatible with each other. At the same time, the relationship between the softening points of the crystalline resin and the amorphous resin is defined.
However, with this technology, although the toner that contributes to the low-temperature fixing of the image can be obtained due to the sharp melt property of the crystalline resin, the blocking resistance may be deteriorated, and the low-temperature fixing and blocking resistance of the image may be deteriorated. It is difficult to achieve both.

  Further, for example, in Japanese Patent Application Laid-Open No. 2006-276044 of Patent Document 4, a crystalline resin and an amorphous resin are contained as a binder resin, and at least a part of them is mutually compatible, so that The glass transition temperature (Tg) is lowered, which is effective for fixing toner at low temperature, and the degree of decrease in the glass transition temperature (Tg) of the toner differs depending on the combination of the resin forming the binder resin. It has been found that there is an easy combination, has good hot offset resistance, and has both excellent blocking resistance and low-temperature fixability. However, this technique may cause a problem of deterioration in heat-resistant storage stability of the toner depending on the compatibility of the crystalline resin.

In recent years, full color toners are required to have high color developability in order to improve image quality. In order for the fixed toner to develop a clear color, the image needs to have high gloss.
As a means for achieving this, there is a method in which the spreadability of the toner at the time of fixing is improved by lowering the viscosity of the melted toner, and the glossiness is increased by making the image surface smoother. However, lowering the viscosity of the toner deteriorates the heat resistance of the toner, so that the hot offset resistance is deteriorated similarly to the low-temperature fixing.
For example, Japanese Patent Application Laid-Open No. 2000-039738 of Patent Document 5 achieves both excellent fixing characteristics and heat resistance by using a cross-linked polyester containing a gel and a non-cross-linked polyester containing no gel. However, this technique is excellent in offset resistance, but the glossiness is not improved.

Further, for example, in Japanese Patent Application Laid-Open No. 2007-148085 of Patent Document 6, a resin having a different flow softening temperature is used together to satisfy fixing characteristics, high glossiness, anti-fusing property, and the like. From the viewpoint of high gloss, it is insufficient.
In addition, oilless toners that contain a release agent in the toner without using oil in the fixing machine are mainly used at present. However, since the toner with low viscosity deteriorates the releasability, sufficient release If the property is not secured, the fixing property is remarkably impaired, and an excessive release agent causes storability and carrier contamination. Japanese Patent Application Laid-Open No. 2004-246435 of Patent Document 7 defines the amount of the release agent on the toner surface by the FT-IR method, but the effect on the toner for the purpose of achieving both low temperature fixing and high gloss is unknown. In addition, it is not sufficient for solving the above-mentioned problems related to the release agent.

  Accordingly, at present, a toner that exhibits high glossiness and a related technology using the toner while providing both excellent low-temperature fixability and hot offset resistance have not yet been provided.

  SUMMARY OF THE INVENTION The present invention has been made in view of the above-described problems of the prior art, and an object thereof is to provide a toner that exhibits high gloss without disturbing low-temperature fixability and hot offset property, and that achieves both high image quality and high releasability. And

As a result of intensive studies, the present inventors have found that the above problems can be solved by the inventions described in the following (1) to (10), and have reached the present invention.
(1) A solution or dispersion of an organic solvent obtained by dissolving or dispersing at least a binder resin, a prepolymer composed of a modified polyester resin, an active hydrogen group compound that extends or crosslinks with the prepolymer, a colorant, and a release agent. A method for producing a toner, in which a liquid is subjected to a crosslinking reaction and / or an extension reaction in an aqueous medium, and a solvent is removed from the obtained O / W dispersion,
The precursor for the prepolymer is an unmodified polyester copolymerized component an alcohol having a carbon ring, the precursor is Ri peak top molecular weight Mpt in the range near the 12000 ≦ Mpt ≦ 28000, and The ratio of the weight average molecular weight Mw to the number average molecular weight Mn, Mw / Mn is 4.5 or less,
The SP value SPr of the binder resin and the SP value SPw of the release agent are in a relationship of 3.0 <| SPr−SPw | <10.0,
And a melting point of the releasing agent is in the range of 50 ° C. to 90 ° C.
(2) The toner production method as described in (1) above, wherein the release agent is a monoester wax.
(3) The toner production method as described in (1) or (2) above, wherein the release agent has a kinematic viscosity at 100 ° C. of less than 10 mPa · s.
(4) The method for producing a toner according to any one of (1) to (3), wherein the isocyanate value of the prepolymer is 0.4 to 0.7 mol%.
(5) The method for producing a toner according to any one of (1) to (4), wherein the prepolymer is contained in an amount of 5 to 13% by weight.
(6) The method for producing a toner according to any one of (1) to (5), wherein the binder resin is a polyester resin.
(7) The method for producing a toner according to any one of (1) to (6), wherein the binder resin contains at least amorphous polyester and crystalline polyester.
(8) The method for producing a toner according to any one of (1) to (7), wherein the toner particles have a volume average particle diameter of 3 to 7 μm.
(9) The above items (1) to (8), wherein the ratio Dv / Dn of the volume average particle diameter Dv to the number average particle diameter Dn of the toner particles of the toner is 1.0 to 1.25. The method for producing a toner according to any one of the above.
(10) The method for producing a toner according to any one of (1) to (9), wherein the toner particles have an average circularity of 0.94 to 0.99.

  As will be understood from the following detailed and specific description, according to the present invention, the molecular weight of the prepolymer precursor contained in the toner and the SP value of the binder resin and the release agent in the toner are controlled. Thus, an extremely excellent effect that a toner having both high glossiness and sufficient releasability can be provided without inhibiting the low-temperature fixability and the hot offset property is exhibited.

1 is a schematic diagram illustrating an example of an image forming apparatus of the present invention. It is a schematic block diagram of an example of a contact-type brush charging device. It is a schematic block diagram of an example of a developing device. FIG. 2 is a schematic configuration diagram of an example of a fixing device. FIG. 3 is a diagram illustrating a layer configuration of a fixing belt. It is a schematic block diagram of an example of the process ridge of this invention. 1 is a schematic configuration diagram of an example of an image forming apparatus of the present invention. It is a schematic block diagram of the other example of the image forming apparatus of this invention.

Hereinafter, the present invention will be specifically described.
In the toner of the present invention, the unmodified polyester (hereinafter referred to as intermediate polyester) which is a precursor for the prepolymer is preferably a polyester having a carbon ring alcohol as a copolymer component. By introducing a carbon ring into the alcohol part of the polyester molecular chain, aggregation of molecules can be suppressed due to steric hindrance, and the viscosity of the toner can be reduced. With straight-chain alcohol alone, the molecules are likely to approach each other sterically, and because the intermolecular distance is short, the molecules strongly aggregate and the viscosity of the toner is not sufficiently reduced.
The peak top molecular weight Mpt of the intermediate polyester (precursor) is preferably 12000 < Mpt <28000, the ratio of the weight average molecular weight Mw to the number average molecular weight Mn, and Mw / Mn is 4.5 or less. preferable.
If the Mpt is less than 12,000, the molecular weight after the extension reaction is small and the hot offset resistance is deteriorated. If the Mpt is greater than 28000, the molecular weight is too large and the toner is not sufficiently lowered in viscosity, and the low-temperature fixability and glossiness are deteriorated. In addition, the increase in molecular weight increases the viscosity of the prepolymer, which is not acceptable from the viewpoint of manufacturability. Mw / Mn means the distribution of molecular weight. When Mw / Mn exceeds 4.5, the ratio of the prepolymer having a molecular weight different from the molecular weight exhibiting the desired thermal characteristics is large, and the low-temperature fixability and high It becomes difficult to balance gloss.

  When the SP value of the binder resin is SPr and the SP value of the release agent is SPw, it is preferable that the relationship of 3.0 <| SPr-SPw | <10.0 is satisfied. If it is less than 3.0, the release agent concentrates inside the toner, so that sufficient release properties cannot be obtained. If it exceeds 10.0, the release agent is excessively exposed on the surface of the toner, and although the releasability can be secured, it causes deterioration of heat resistant storage stability and carrier contamination.

Examples of the functional group capable of reacting with the active hydrogen group-containing compound of the prepolymer include an isocyanate group, an epoxy group, a carboxyl group, and the like, and a polyester having an isocyanate group [hereinafter referred to as prepolymer (A)]. It is preferable.
Examples of the active hydrogen group of the compound having an active hydrogen group include a hydroxyl group (alcoholic hydrogen group and phenolic hydroxyl group), an amino group, a carboxyl group, a mercapto group, and the like, and an alcoholic hydroxyl group and an amino group are preferable. .

Hereinafter, the case where the prepolymer (A) is used as a polymer having a functional group capable of reacting with an active hydrogen group and the case where an amine (B) is used as a compound having an active hydrogen group will be described.
The urea-modified polyester obtained by reacting the prepolymer (A) with amines (B) as a crosslinking agent and / or extender is easy to adjust the molecular weight of the high molecular weight component, and is particularly suitable for dry toners, This is preferable because oilless low-temperature fixing characteristics (a wide range of releasability and fixing ability without an oil application mechanism to a fixing heating medium) can be secured. Among them, a urea-modified polyester having a terminal modified is particularly preferable because oil-less low-temperature fixing characteristics can be secured while maintaining high fluidity and transparency in the fixing temperature range of the polyester.

The prepolymer (A) can be obtained, for example, by reacting a polyester having an active hydrogen group (intermediate polyester, precursor) with polyisocyanate (PIC). Examples of the active hydrogen group possessed by the polyester include hydroxyl groups (alcoholic hydrogen groups and phenolic hydroxyl groups), amino groups, carboxyl groups, mercapto groups, and the like, with alcoholic hydroxyl groups being preferred.
A polyester having an alcoholic hydroxyl group as an active hydrogen group can be obtained by polycondensation of a polyol (PO) and a polycarboxylic acid (PC).
Examples of the polyol (PO) include a diol (DIO) and a trivalent or higher polyol (TO), and a diol (DIO) or a combination of a diol (DIO) and a trivalent or higher polyol (TO) is preferable.

  Diols having carbon rings in the molecule (DIO) include alicyclic diols (1,4-cyclohexanedimethanol, hydrogenated bisphenol A, etc.); bisphenols (bisphenol A, bisphenol F, bisphenol S, etc.); Alkylene oxide (ethylene oxide, propylene oxide, butylene oxide, etc.) adducts of cyclic diols; alkylene oxide (ethylene oxide, propylene oxide, butylene oxide, etc.) adducts of the above bisphenols, etc. Also good. Among these, alkylene oxide adducts of bisphenols having 2 to 12 carbon atoms are preferred, and combined use of alkylene oxide adducts of bisphenols or alkylene oxide adducts of bisphenols and alkylene glycols having 2 to 12 carbon atoms is particularly preferred.

  Examples of the trihydric or higher polyol (TO) include trihydric or higher phenols (trisphenol PA, phenol novolak, cresol novolak, etc.); trihydric or higher polyphenol alkylene oxide adducts, etc. May be.

  Examples of the polycarboxylic acid (PC) include dicarboxylic acid (DIC) and trivalent or higher polycarboxylic acid (TC). Dicarboxylic acid (DIC) or dicarboxylic acid (DIC) and trivalent or higher polycarboxylic acid ( TC) is preferred.

  Dicarboxylic acids (DIC) include alkylene dicarboxylic acids (succinic acid, adipic acid, sebacic acid, etc.); alkenylene dicarboxylic acids (maleic acid, fumaric acid, etc.); aromatic dicarboxylic acids (phthalic acid, isophthalic acid, terephthalic acid, naphthalene) Dicarboxylic acid and the like), and two or more of them may be used in combination. Among these, alkenylene dicarboxylic acids having 4 to 20 carbon atoms and aromatic dicarboxylic acids having 8 to 20 carbon atoms are preferable.

Examples of the trivalent or higher polycarboxylic acid (TC) include aromatic polycarboxylic acids having 9 to 20 carbon atoms (trimellitic acid, pyromellitic acid, etc.), and two or more kinds may be used in combination.
In place of polycarboxylic acid (PC), polycarboxylic acid (PC) anhydride or lower alkyl ester (methyl ester, ethyl ester, isopropyl ester, etc.) may be used.

  When synthesizing a polyester having an alcoholic hydroxyl group, the water produced is heated to 150-280 ° C. in the presence of a known esterification catalyst such as tetrabutoxytitanate, dibutyltin oxide, etc. It is preferable to leave. At this time, the equivalent ratio of the hydroxyl group to the carboxyl group is usually 1 to 2, preferably 1 to 1.5, and more preferably 1.02 to 1.3.

  As polyisocyanate (PIC), aliphatic polyisocyanate (tetramethylene diisocyanate, hexamethylene diisocyanate, 2,6-diisocyanatomethylcaproate, etc.); alicyclic polyisocyanate (isophorone diisocyanate, cyclohexylmethane diisocyanate, etc.); aromatic Diisocyanates (tolylene diisocyanate, diphenylmethane diisocyanate, etc.); araliphatic diisocyanates (α, α, α ′, α′-tetramethylxylylene diisocyanate, etc.); isocyanurates; block these with phenol derivatives, oximes, caprolactam, etc. 2 or more types may be used in combination.

  When the polyester having an alcoholic hydroxyl group is reacted with polyisocyanate (PIC), the reaction is preferably performed at 40 to 140 ° C. At this time, the equivalent ratio of the isocyanate group to the alcoholic hydroxyl group is usually 1 to 5, preferably 1.2 to 4, and more preferably 1.5 to 2.5. When this equivalent ratio exceeds 5, the low-temperature fixability of the toner may be lowered. When the equivalent ratio is less than 1, the urea group content decreases and the hot offset resistance is reduced when a urea-modified polyester is synthesized. May decrease.

  Moreover, when reacting polyester which has alcoholic hydroxyl group, and polyisocyanate (PIC), you may add a solvent as needed. Solvents include aromatic solvents (toluene, fxylene, etc.); ketones (acetone, methyl ethyl ketone, methyl isobutyl ketone, etc.); esters (ethyl acetate, etc.); amides (dimethylformamide, dimethylacetamide, etc.), ethers ( Examples thereof include solvents inert to isocyanates such as tetrahydrofuran.

  Content of the structural component derived from polyisocyanate (PIC) in a prepolymer (A) is 0.5-40 mass% normally, 1-30 mass% is preferable, and 2-20 mass% is more preferable. When this content is less than 0.5% by mass, the hot offset resistance is lowered and the heat resistant storage stability and the low temperature fixability may not be compatible. When the content exceeds 40% by mass, the low temperature fixability is deteriorated. There are things to do.

  Examples of the amines (B) include a diamine (B1), a trivalent or higher polyamine (B2), an aminoalcohol (B3), an aminomercaptan (B4), an amino acid (B5), and a block of these amino groups (B6). Among them, diamine (B1) or a combination of diamine (B1) and a trivalent or higher polyamine (B2) is preferable.

  Examples of the diamine (B1) include aromatic diamines (phenylenediamine, diethyltoluenediamine, 4,4′-diaminodiphenylmethane, etc.); alicyclic diamines (4,4′-diamino-3,3′-dimethyldicyclohexylmethane, diamino). Cyclohexane, isophorone diamine, etc.); aliphatic diamines (ethylene diamine, tetramethylene diamine, hexamethylene diamine, etc.) and the like, and two or more of them may be used in combination.

Examples of the trivalent or higher polyamine (B2) include diethylenetriamine and triethylenetetramine, and two or more kinds may be used in combination.
Examples of the amino alcohol (B3) include ethanolamine and hydroxyethylaniline, and two or more kinds may be used in combination.
Examples of amino mercaptan (B4) include aminoethyl mercaptan and aminopropyl mercaptan, and two or more of them may be used in combination.
Examples of the amino acid (B5) include aminopropionic acid and aminocaproic acid, and two or more kinds may be used in combination.
Examples of these blocked amino groups (B6) include ketimine compounds and oxazolidine compounds obtained from amines and ketones (acetone, methyl ethyl ketone, methyl isobutyl ketone, etc.), and two or more of them may be used in combination. .

In the present invention, the modified polyester can be produced by a one-shot method or the like.
For example, when the prepolymer (A) and the amines (B) are reacted, a known catalyst such as dibutyltin laurate or dioctyltin laurate may be used as necessary. At this time, although reaction time is suitably selected according to the combination of prepolymer (A) and amines (B), for example, it is 10 minutes-40 hours normally, and 2-24 hours are preferable. The reaction temperature is usually 0 to 150 ° C, preferably 40 to 98 ° C.

  When the prepolymer (A) and the amines (B) are reacted, the equivalent ratio of the isocyanate group to the amino group is usually 0.5 to 2, preferably 2/3 to 1.5, 5/6 to 1.2. When this equivalent ratio exceeds 2 and is less than 0.5, the molecular weight of the urea-modified polyester is decreased, and the hot offset resistance may be lowered.

Moreover, when making a prepolymer (A) and amines (B) react, the molecular weight of a urea modified polyester can be adjusted using an elongation terminator as needed.
Examples of the elongation terminator include monoamines (diethylamine, dibutylamine, butylamine, laurylamine, etc.), those blocked (ketimine compounds), and the like.

In the present invention, when preparing the oil phase, modified polyesters such as urea-modified polyester and urethane-modified polyester may be added together with the prepolymer (A).
The urea-modified polyester may have a urethane bond together with a urea bond.
The molar ratio of the urethane bond to the urea bond is usually 0 to 9, preferably 0.25 to 4, more preferably 2/3 to 7/3. When this molar ratio exceeds 9, the hot offset resistance may decrease.

  In addition, when making a prepolymer (A) and amines (B) react, you may add a solvent as needed. Solvents include aromatic solvents (toluene, xylene, etc.); ketones (acetone, methyl ethyl ketone, methyl isobutyl ketone, etc.); esters (ethyl acetate, etc.); amides (dimethylformamide, dimethylacetamide, etc.), ethers (tetrahydrofuran) And a solvent inert to the isocyanate.

  When the polyester is not added when preparing the oil phase, the modified polyester usually has a number average molecular weight of 2000 to 15000, preferably 2000 to 10000, and more preferably 2000 to 8000. When the number average molecular weight is less than 2,000, the developed paper may be wound around the fixing roller, and when it exceeds 15,000, the low temperature fixability and the glossiness when used in a full color apparatus may be deteriorated.

In the present invention, when preparing the oil phase, it is preferable to add polyester together with (prepolymer (A). This makes it possible to achieve both heat-resistant storage stability and low-temperature fixability of the toner.
Polyester can be obtained by polycondensation of polyol (PO) and polycarboxylic acid (PC) in the same manner as described above.

The polyester preferably has a weight-average molecular weight of 1000 to 30000 in THF-soluble matter. When the weight-average molecular weight of the THF-soluble component is less than 1000, the oligomer component increases, and the heat-resistant storage stability may decrease. Moreover, when the weight average molecular weight of THF-soluble matter exceeds 30000, when the polyester is added together with the prepolymer (A) when preparing the oil phase, the prepolymer (A) and amines are added due to steric hindrance. The reaction with (B) does not proceed sufficiently, and offset resistance may decrease.
In the present invention, the number average molecular weight and the weight average molecular weight are molecular weights in terms of polystyrene measured using GPC (gel permeation chromatography).

The polyester preferably has an acid value of 1 to 50 KOHmg / g. When the acid value is less than 1 KOH mg / g, the dispersion stabilizing effect due to the addition of the basic compound may not be obtained when the toner is produced. In addition, when the polyester is added together with the prepolymer (A) and the amines (B) when preparing the oil phase, the reaction between the prepolymer (A) and the amines (B) is likely to proceed, so that Problems with stability may arise. On the other hand, when the acid value exceeds 50 KOHmg / g, when the polyester is added together with the prepolymer (A) and the amines (B) when preparing the oil phase, the prepolymer (A) and the amines (B) This reaction may not proceed sufficiently, and offset resistance may decrease.
In the present invention, the acid value can be measured according to the measurement method described in JIS K0070-1992.

  The polyester preferably has a glass transition point of 35 to 65 ° C. When the glass transition point is less than 35 ° C, the heat-resistant storage stability of the toner may be lowered, and when it exceeds 65 ° C, the low-temperature fixability may be lowered.

In addition, the combined use of urea-modified polyester and polyester can improve low-temperature fixability and gloss when used in a full-color device. For example, the polyester can be dissolved in a solution obtained by reacting the prepolymer (A) and the amines (B).
Further, urea-modified polyester and urethane-modified polyester may be used in combination.

  When the urea-modified polyester and the polyester are used in combination, the urea-modified polyester is preferably compatible with at least a part of the polyester in terms of low-temperature fixability and hot offset resistance. For this reason, the polyester component of the urea-modified polyester is preferably similar in composition to the polyester.

  The mass ratio of the urea-modified polyester to the polyester is usually 5/95 to 80/20, preferably 5/95 to 30/70, more preferably 5/95 to 25/75, and 7/93 to 20/80. Is particularly preferred. When this mass ratio is less than 5/95, the hot offset resistance is lowered, and it may be disadvantageous in terms of both heat-resistant storage stability and low-temperature fixability. When it exceeds 80/20, low-temperature fixability is obtained. May decrease.

  The content of the polyester contained in the binder resin is preferably 50 to 100% by mass. If this content is less than 50% by mass, it may be difficult to achieve both heat-resistant storage stability and low-temperature fixability of the toner.

As the colorant used in the present invention, all known dyes and pigments can be used. For example, carbon black, nigrosine dye, iron black, naphthol yellow S, Hansa yellow (10G, 5G, G), cadmium yellow, yellow Iron oxide, ocher, yellow lead, titanium yellow, polyazo yellow, oil yellow, Hansa yellow (GR, A, RN, R), pigment yellow L, benzidine yellow (G, GR), permanent yellow (NCG), Vulcan fast Yellow (5G, R), Tartrazine Lake, Quinoline Yellow Lake, Anthrazan Yellow BGL, Isoindolinone Yellow, Bengala, Red Dan, Lead Zhu, Cadmium Red, Cadmium Mercury Red, Antimon Zhu, Permanent Red 4R , Para red, phissa red, parac Luort Nitroaniline Red, Resol Fast Scarlet G, Brilliant Fast Scarlet, Brilliant Carnmin BS, Permanent Red (F2R, F4R, FRL, FRLL, F4RH), Fast Scarlet VD, Belkan Fast Rubin B, Brilliant Scarlet G, Resol Rubin GX, Permanent Red F5R, Brilliant Carmine 6B, Pigment Scarlet 3B, Bordeaux 5B, Tolujing Maroon, Permanent Bordeaux F2K, Helio Bordeaux BL, Bordeaux 10B, Bon Maroon Light, Bon Maroon Medium, Eosin Lake, Rhodamine Lake B, Rhodamine Lake Y, Alizarin Lake, thioindigo red B, thioindigo maroon, oil red, quinacridone red, pi Zoron Red, Polyazo Red, Chrome Vermillion, Benzidine Orange, Perinone Orange, Oil Orange, Cobalt Blue, Cerulean Blue, Alkaline Blue Lake, Peacock Blue Lake, Victoria Blue Lake, Metal Free Phthalocyanine Blue, Phthalocyanine Blue, Fast Sky Blue, Indance Ren Blue (RS, BC), Indigo, Ultramarine Blue, Bitumen, Anthraquinone Blue, Fast Violet B, Methyl Violet Lake, Cobalt Purple, Manganese Purple, Dioxane Violet, Anthraquinone Violet, Chrome Green, Zinc Green, Chrome Oxide, Pyridian, Emerald Green , Pigment Green B, Naphthol Green B, Green Gold, Acid Green Lake, Malachite Gree Lake, phthalocyanine green, anthraquinone green, titanium oxide, zinc white, lithopone and mixtures thereof can be used.
The content of the colorant is usually 1 to 15% by weight, preferably 3 to 10% by weight, based on the toner.

The colorant used in the present invention can also be used as a master batch combined with a resin.
As the binder resin to be kneaded together with the production of the masterbatch or the masterbatch, in addition to the modified and unmodified polyester resins mentioned above, styrene such as polystyrene, poly p-chlorostyrene, polyvinyltoluene, and polymers of substituted products thereof; Styrene-p-chlorostyrene copolymer, styrene-propylene copolymer, styrene-vinyltoluene copolymer, styrene-vinylnaphthalene copolymer, styrene-methyl acrylate copolymer, styrene-ethyl acrylate copolymer Styrene-butyl acrylate copolymer, styrene-octyl acrylate copolymer, styrene-methyl methacrylate copolymer, styrene-ethyl methacrylate copolymer, styrene-butyl methacrylate copolymer, styrene-α- Chloromethyl methacrylate copolymer, Tylene-acrylonitrile copolymer, styrene-vinyl methyl ketone copolymer, styrene-butadiene copolymer, styrene-isoprene copolymer, styrene-acrylonitrile-indene copolymer, styrene-maleic acid copolymer, styrene-malein Styrene copolymers such as acid ester copolymers; polymethyl methacrylate, polybutyl methacrylate, polyvinyl chloride, polyvinyl acetate, polyethylene, polypropylene, polyester, epoxy resin, epoxy polyol resin, polyurethane, polyamide, polyvinyl butyral, poly Acrylic resin, rosin, modified rosin, terpene resin, aliphatic or alicyclic hydrocarbon resin, aromatic petroleum resin, chlorinated paraffin, paraffin wax, etc. The

This master batch can be obtained by mixing and kneading a resin for a master batch and a colorant under a high shear force to obtain a master batch.
In this case, an organic solvent can be used in order to enhance the interaction between the colorant and the resin.
Also, a so-called flushing method called watering paste containing water of colorant is mixed and kneaded with resin and organic solvent, and the colorant is transferred to the resin side to remove moisture and organic solvent components. Since it can be used as it is, it does not need to be dried and is preferably used.
For mixing and kneading, a high shear dispersion device such as a three-roll mill is preferably used.

Known release agents may be used in the present invention, such as ester wax, polyolefin wax (polyethylene wax, polypropylene wax, etc.); long-chain hydrocarbons (paraffin wax, sasol wax, etc.); Examples thereof include carbonyl group-containing waxes.
Among these, ester wax is preferable, and monoester wax is particularly preferable.
The melting point of the wax of the present invention is usually in the range of 50 ° C to 90 ° C, and preferably in the range of 50 ° C to 80 ° C. A wax having a melting point of less than 80 ° C. has an adverse effect on heat-resistant storage stability, and a wax having a melting point of more than 80 ° C. tends to cause a cold offset when fixing at a low temperature.
Moreover, it is preferable that the viscosity of a wax is 10 mPa * s or less as a kinematic viscosity of 100 degreeC. Waxes exceeding 10 mPa · s have poor effects for improving hot offset resistance and low-temperature fixability.
The content of the wax in the toner is preferably 3 to 30% by weight.

(Charge control agent)
The toner of the present invention may contain a charge control agent as necessary.
All known charge control agents can be used, such as nigrosine dyes, triphenylmethane dyes, chromium-containing metal complex dyes, molybdate chelate pigments, rhodamine dyes, alkoxy amines, quaternary ammonium salts (fluorine-modified). Quaternary ammonium salts), alkylamides, phosphorus simple substances or compounds, tungsten simple substances or compounds, fluorine-based activators, salicylic acid metal salts, and metal salts of salicylic acid derivatives.
Specifically, Nitronine-based dye Bontron 03, quaternary ammonium salt Bontron P-51, metal-containing azo dye Bontron S-34, oxynaphthoic acid metal complex E-82, salicylic acid metal complex E- 84, E-89 of a phenol-based condensate (manufactured by Orient Chemical Industry Co., Ltd.), TP-302 of a quaternary ammonium salt molybdenum complex, TP-415 (manufactured by Hodogaya Chemical Industry Co., Ltd.), quaternary ammonium Copy charge PSYVP2038 of salt, copy blue PR of triphenylmethane derivative, copy charge NEGVP2036 of quaternary ammonium salt, copy charge NXVP434 (above, manufactured by Hoechst), LRA-901, LR-147 which is a boron complex (Nippon Carlit) ), Copper phthalocyanine, perylene, quinacridone, a System pigment, a sulfonic acid group, a carboxyl group, and polymer compounds having a functional group such as a quaternary ammonium salt.

In the present invention, the amount of charge control agent used is determined uniquely by the type of toner binder resin, the presence or absence of additives used as necessary, and the toner production method including the dispersion method, and is uniquely limited. However, it is preferably used in the range of 0.1 to 10 parts by weight with respect to 100 parts by weight of the toner binder resin.
More preferably, the range of 0.2 to 5 parts by weight is good.
When the amount exceeds 10 parts by weight, the chargeability of the toner is too high, the effect of the main charge control agent is reduced, the electrostatic attractive force with the developing roller is increased, the flowability of the developer is reduced, and the image density is reduced. Incurs a decline.
These charge control agents can be dissolved and dispersed after being melt-kneaded with a masterbatch and resin, or of course, may be added when directly dissolving or dispersing in an organic solvent, or may be fixed on the toner surface after preparation of toner particles. May be.

(Resin fine particles)
The resin fine particles used in the present invention preferably have a glass transition point (Tg) of 50 to 70 ° C. When the glass transition point (Tg) is less than 50 ° C., the toner storage stability is deteriorated and stored. Sometimes, blocking may occur in the developing machine.
When the glass transition point (Tg) is higher than 70 ° C., the resin fine particles may interfere with the adhesion to the fixing paper, and the minimum fixing temperature may increase.
The weight average molecular weight is desirably 100,000 or less.
Preferably it is 50,000 or less.
The lower limit is usually 4000.
When the weight average molecular weight exceeds 100,000, the resin fine particles may inhibit the adhesion to the fixing paper, and the minimum fixing temperature may increase.

The resin fine particles may be any resin as long as it can form an aqueous dispersion, and may be a thermoplastic resin or a thermosetting resin. For example, vinyl resin, polyurethane resin, epoxy resin, polyester resin, polyamide resin, Examples include polyimide resins, silicon resins, phenol resins, melamine resins, urea resins, aniline resins, ionomer resins, and polycarbonate resins.
As the resin fine particles, two or more of the above resins may be used in combination.
Of these, preferred is a vinyl resin, a polyurethane resin, an epoxy resin, a polyester resin, or a combination resin thereof because an aqueous dispersion of fine spherical resin particles is easily obtained.

Examples of the vinyl resin include polymers obtained by homopolymerization or copolymerization of vinyl monomers, such as styrene- (meth) acrylic acid ester resins, styrene-butadiene copolymers, and (meth) acrylic acid-acrylic acid ester polymers. Styrene-acrylonitrile copolymer, styrene-maleic anhydride copolymer, styrene- (meth) acrylic acid copolymer, and the like.
In the resin fine particles, the average particle size is preferably 5 to 200 nm, more preferably 20 to 150 nm.

(External additive)
As the external additive for assisting the fluidity, developability and chargeability of the colored resin particles (toner base particles) obtained in the present invention, inorganic fine particles can be preferably used.
The primary particle diameter of the inorganic fine particles is preferably 5 nm to 100 nm, and particularly preferably 10 nm to 50 nm.
Moreover, it is preferable that the specific surface area by BET method is 20-500 m < ² > / g.
The proportion of the inorganic fine particles used is preferably 0.01 to 5% by weight of the toner, and particularly preferably 0.01 to 2.0% by weight.
Specific examples of the inorganic fine particles include, for example, silica, alumina, titanium oxide, barium titanate, magnesium titanate, calcium titanate, strontium titanate, zinc oxide, tin oxide, quartz sand, clay, mica, wollastonite, diatomaceous earth. Examples include soil, chromium oxide, cerium oxide, pengala, antimony trioxide, magnesium oxide, zirconium oxide, barium sulfate, barium carbonate, calcium carbonate, silicon carbide, and silicon nitride.

  Other polymer fine particles such as polystyrene, methacrylic acid ester and acrylic acid ester copolymer obtained by soap-free emulsion polymerization, suspension polymerization, and dispersion polymerization, polycondensation systems such as silicone, benzoguanamine, and nylon, and thermosetting resins Examples include polymer particles.

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

A cleaning improver for removing the developer after transfer remaining on the photoreceptor or the primary transfer medium may be added. Examples of the cleaning improver include fatty acid metals such as zinc stearate, calcium stearate, and stearic acid. Examples thereof include polymer fine particles produced by a salt-free emulsion polymerization such as polymethyl methacrylate fine particles and polystyrene fine particles.
The polymer fine particles preferably have a relatively narrow particle size distribution and a volume average particle size of 0.01 to 1 μm.

(Production method)
The toner binder can be produced by the following method.
Polyester having a hydroxyl group by heating the polyol and polycarboxylic acid to 150-280 ° C. in the presence of a known esterification catalyst such as tetrabutoxy titanate, dibutyltin oxide, etc., and distilling off the water generated while reducing the pressure as necessary. Get.
Next, this is reacted with polyisocyanate at 40 to 140 ° C. to obtain a prepolymer (A) having an isocyanate group.
Further, this A is reacted with amines (B) at 0 to 140 ° C. to obtain a polyester modified with a urea bond.
When the polyisocyanate is reacted and when A and B are reacted, a solvent can be used if necessary.
Usable solvents include aromatic solvents (toluene, xylene, etc.); ketones (acetone, methyl ethyl ketone, methyl isobutyl ketone, etc.); esters (ethyl acetate, etc.); amides (dimethylformamide, dimethylacetamide, etc.) and ethers And those inert to polyisocyanates (PIC) such as tetrahydrofuran (such as tetrahydrofuran).
When using a polyester (PE) not modified with a urea bond, this PE is produced in the same manner as in the case of a polyester having a hydroxyl group, and this is dissolved in a solution after completion of the reaction of the urea-modified polyester. Mix.

(Manufacture of toner)
The dry toner of the present invention can be produced by the following method, but is not limited thereto.

(Toner production method in aqueous medium)
As an aqueous medium, water alone may be used, but a solvent miscible with water may be used in combination.
Examples of the miscible solvent include alcohol (methanol, isopropanol, ethylene glycol, etc.), dimethylformamide, tetrahydrofuran, cellosolves (methylcellosolve, etc.), lower ketones (acetone, methyl ethyl ketone, etc.) and the like.

The toner particles can be formed by reacting a dispersion composed of a prepolymer (A) having an isocyanate group with an amine (B) in an aqueous medium.
As a method for stably forming a dispersion composed of urea-modified polyester or prepolymer (A) in an aqueous medium, the composition of a toner raw material composed of urea-modified polyester or prepolymer (A) is added to the aqueous medium. And a method of dispersing by shearing force.
The colorant, colorant masterbatch, release agent, charge control agent, unmodified polyester resin, etc. which are the prepolymer (A) and other toner components (hereinafter referred to as toner raw materials) are dispersed in an aqueous medium. It may be mixed at the time of formation, but it is more preferable to mix the toner raw materials in advance and then add and disperse the mixture in the aqueous medium.
In the present invention, other toner raw materials such as a colorant, a release agent, and a charge control agent do not necessarily have to be mixed when forming particles in an aqueous medium. It may be added later.
For example, after forming particles containing no colorant, the colorant can be added by a known dyeing method.

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

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

In the step of synthesizing the urea-modified polyester from the prepolymer (A), the amines (B) may be added and reacted before the toner composition is dispersed in the aqueous medium, or the amines may be reacted after being dispersed in the aqueous medium. (B) may be added to cause a reaction from the particle interface.
In this case, urea-modified polyester is preferentially generated on the surface of the toner to be produced, and a concentration gradient can be provided inside the particles.

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

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

  Product names include Surflon S-111, S-112, S-113 (Asahi Glass Co., Ltd.), Florard FC-93, FC-95, FC-98, FC-129 (Sumitomo 3M Co., Ltd.), Unidyne DS-101. DS-102 (Daikin Kogyo Co., Ltd.), MegaFuck F-110, F-120, F-113, F-191, F-812, F-833 (Dainippon Ink Co., Ltd.), Xtop EF-102 , 103, 104, 105, 112, 123A, 123B, 306A, 501, 201, 204 (manufactured by Tochem Products), and Fgentent F-100, F150 (manufactured by Neos).

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

  In addition, calcium phosphate, calcium carbonate, titanium oxide, colloidal silica, hydroxyapatite, and the like can also be used as inorganic compound dispersants that are hardly soluble in water.

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

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

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

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

When the modified polyester capable of reacting with active hydrogen is reacted with an amine (B) as a crosslinking agent and / or extender, the elongation and / or crosslinking reaction time is determined by the isocyanate group structure and amine of the prepolymer (A). Although it is selected depending on the reactivity due to the combination with class (B), it is usually 10 minutes to 40 hours, preferably 2 to 24 hours.
The reaction temperature is usually 0 to 150 ° C., preferably 40 to 98 ° C.
Moreover, a well-known catalyst can be used as needed.
Specific examples include dibutyltin laurate and dioctyltin laurate.

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

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

By mixing the resulting dried toner powder with dissimilar particles such as release agent fine particles, charge control fine particles, fluidizing agent fine particles, and colorant fine particles, or by giving mechanical impact force to the mixed powder By immobilizing and fusing on the surface, it is possible to prevent detachment of the foreign particles from the surface of the resulting composite particle.
Specific means include a method of applying an impact force to the mixture by blades rotating at high speed, a method of injecting and accelerating the mixture in a high-speed air stream, and causing particles or composite particles to collide with an appropriate collision plate, etc. is there.
As equipment, Ong mill (manufactured by Hosokawa Micron Co., Ltd.), I-type mill (manufactured by Nippon Pneumatic Co., Ltd.) is modified to reduce the grinding air pressure, hybridization system (manufactured by Nara Machinery Co., Ltd.), kryptron system (Made by Kawasaki Heavy Industries, Ltd.), automatic mortar and the like.

(Carrier for two-component developer)
When the toner of the present invention is used for a two-component developer, it may be used by mixing with a magnetic carrier, and the content ratio of the carrier and the toner in the developer is 1 to 10 weights of toner with respect to 100 parts by weight of the carrier. Part is preferred.
As the magnetic carrier, conventionally known ones such as iron powder, ferrite powder, magnetite powder, magnetic resin carrier having a particle diameter of about 20 to 200 μm can be used.
The carrier surface may be coated, and examples of the coating material include amino resins such as urea-formaldehyde resin, melamine resin, benzoguanamine resin, urea resin, polyamide resin, and epoxy resin.
Polyvinyl and polyvinylidene resins such as acrylic resins, polymethyl methacrylate resins, polyacrylonitrile resins, polyvinyl acetate resins, polyvinyl alcohol resins, polyvinyl butyral resins, polystyrene resins and styrene acrylic copolymer resins, Halogenated olefin resins such as vinyl, polyester resins such as polyethylene terephthalate resin and polybutylene terephthalate resin, polycarbonate resins, polyethylene resins, polyvinyl fluoride resins, polyvinylidene fluoride resins, polytrifluoroethylene resins, polyhexafluoro Propylene resin, copolymer of vinylidene fluoride and acrylic monomer, copolymer of vinylidene fluoride and vinyl fluoride, tetrafluoroethylene and vinylidene fluoride And fluoro such as terpolymers of non-fluoride monomers including, and silicone resins.
Moreover, you may contain electrically conductive powder etc. in coating resin as needed.
As the conductive powder, metal powder, carbon black, titanium oxide, tin oxide, zinc oxide or the like can be used.
These conductive powders preferably have an average particle diameter of 1 μm or less.
When the average particle diameter is larger than 1 μm, it becomes difficult to control electric resistance.

  The toner of the present invention can also be used as a one-component magnetic toner that does not use a carrier or a non-magnetic toner.

[Image forming apparatus and image forming method]
An image forming apparatus and an image forming method using the toner of the present invention, for example, a full-color image forming apparatus and an image forming method include a charging step of charging an electrophotographic photosensitive member with a charging unit, and exposure on the charged electrophotographic photosensitive member. An exposure process for forming an electrostatic latent image by means, a development process for forming a toner image by a developing means containing toner on the electrophotographic photosensitive member on which the electrostatic latent image is formed, and on the electrophotographic photosensitive member A primary transfer step of transferring the formed toner image onto an intermediate transfer member by a primary transfer unit; and a secondary transfer step of transferring the toner image transferred onto the intermediate transfer member onto a recording material by a secondary transfer unit; A fixing step of fixing the toner image transferred on the recording material onto the recording material by a fixing means including a heat and pressure fixing member; and transferring the toner image onto the intermediate transfer member by the primary transfer means. And a cleaning step of cleaning by the electrophotographic photosensitive member cleaning means to transfer residual toner adhering to the surface of the. The toner used in the development process is the above-described toner of the present invention. In the full-color image forming method of the present invention, in the secondary transfer step, the linear velocity of transfer of the toner image to the recording material is 100 to 1000 mm / sec, and the transfer time at the nip portion of the secondary transfer means is 0.5. It is preferable to set it to -60 msec. The full color image forming method of the present invention preferably employs a tandem electrophotographic image forming process.

(Charging process, charging means)
As the charging means (device) used in the image forming method of the present invention, for example, the contact type charging device shown in FIGS. 1 and 2 can be used.

FIG. 1 is a view showing an example of a conventionally known image forming apparatus (electrophotographic copying machine) that can be applied when forming an image using toner obtained by the toner manufacturing method according to the present invention.
In FIG. 1, an electrophotographic copying machine (100) has a charger (120) disposed around a photosensitive drum (110) that rotates in the direction A in the drawing, and a laser corresponding to an image read from an original. Light (130) is irradiated. Further, a developing device (140), a transfer device (150), a cleaning device (160), a static elimination lamp (170), and a paper feeding device (180) are disposed around the photosensitive drum (110). . The developing device (140) includes developing rollers (141) and (142), a paddle-like stirring member (143), a stirring member (144), a doctor (145), a toner supply unit (146), and a supply roller. (147). The cleaning device (160) includes a cleaning blade (161) and a cleaning brush (162). Note that guide rails (191) and (192) for attaching / detaching or supporting the developing device (140) are arranged above and below the developing device (140).

<Fur brush type charging device>
The shape of the charging device used in the present invention may take any form, such as a magnetic brush type charging device or a fur brush type charging device, in addition to the roller type charging device, according to the specifications and form of the electrophotographic apparatus. Can be selected. When a magnetic brush charging device is used, the magnetic brush is composed of various ferrite particles such as Zn-Cu ferrite as a charging member, a non-magnetic conductive sleeve for supporting the charging member, and a magnet roll included therein. The In addition, when using a fur brush type charging device, for example, as a material of the fur brush, a fur treated with carbon, copper sulfide, metal, and metal oxide is used, and this is used as a metal or other conductive treated core. A charging device is formed by winding or sticking on gold.

  FIG. 2 shows a schematic configuration of an example of a contact-type brush charging device (510). A photoconductor (515) as an image carrier as a member to be charged is driven to rotate at a predetermined speed (process speed) in the direction of the arrow. A fur brush roller (511) constituted by a fur brush is brought into contact with the photoconductor (515) with a predetermined nip width with a predetermined pressing force against the elasticity of the brush portion (513).

  The fur brush roller (511) as a contact charging device in this example is composed of a metal cored bar (512) having a diameter of 6 mm which also serves as an electrode, and a conductive rayon fiber REC manufactured by Unitika Ltd. as a brush part (513). A tape with -B piled is wound spirally into a roll brush with an outer diameter of 14 mm and a longitudinal length of 250 mm. The brush of the brush portion (513) has a density of 300 denier / 50 filaments and 155 brushes per square millimeter. This roll brush was inserted into a pipe having an inner diameter of 12 mm while rotating in one direction, and the brush and the pipe were set to be concentric, and left in a high-temperature and high-humidity atmosphere to bend and bevel.

The resistance value of the fur brush roller (511) is 1 × 10 ⁵ Ω at an applied voltage of 100V. This resistance value was converted from the current that flows when a fur brush roller is brought into contact with a metal drum having a diameter of φ30 mm with a nip width of 3 mm and a voltage of 100 V is applied. The resistance value of the brush-type charging device (510) is such that even when a low-voltage defective portion such as a pinhole is generated on the photosensitive member (515) to be charged, an excessive leak current flows into this portion. In order to prevent an image defect in which the nip portion is poorly charged, it is necessary to be 10 ⁴ Ω or more, and in order to sufficiently inject charges onto the surface of the photoreceptor (515), it is necessary to be 10 ⁷ Ω or less.

  As the material of the brush, in addition to REC-B manufactured by Unitika Ltd., REC-C, REC-M1, REC-M10, SA-7 manufactured by Toray Industries, Inc., manufactured by Nippon Kashiwa Co., Ltd. Possible examples include Sanderlon, Kanebo Beltron, Kuraray Co., Ltd., Krabobo, carbon dispersion in rayon, Mitsubishi Rayon Co., Ltd. global. One brush is 3 to 10 denier, and preferably has a density of 10 to 100 filaments / bundle and 80 to 600 brushes / mm. The hair foot is preferably 1 to 10 mm.

The fur brush roller (511) is rotationally driven at a predetermined peripheral speed (surface speed) in a direction (counter) opposite to the rotation direction of the photoconductor (515), and contacts the photoconductor surface with a speed difference. A predetermined charging voltage is applied to the brush roller (511) from the power source (514), so that the surface of the rotating photosensitive member is uniformly contact-charged to a predetermined polarity and potential.
In this example, the contact charging of the photoreceptor (515) by the fur brush roller (511) is performed by direct injection charging, and the surface of the rotating photoreceptor is almost equal to the applied charging voltage to the fur brush roller (511). Charged to potential.
In addition to the fur brush roller (511), the charging member used in the present invention may take any form such as a charging roller or a fur brush, and can be selected according to the specifications and form of the electrophotographic apparatus. is there. When a charging roller is used, it is generally used by coating a medium resistance rubber layer of about 100,000 Ω · cm on a cored bar. In the case of using a magnetic brush, the magnetic brush is composed of various ferrite particles such as Zn—Cu ferrite as a charging member, a non-magnetic conductive sleeve for supporting it, and a magnet roll included therein.

  As a magnetic brush as a contact charging member in this example, Zn—Cu ferrite particles having an average particle diameter of 25 μm and Zn—Cu ferrite particles having an average particle diameter of 10 μm are mixed at a weight ratio of 1: 0.05, Magnetic particles obtained by coating ferrite particles having an average particle diameter of 25 μm and having a peak at each average particle diameter position with a medium resistance resin layer were used. The contact charging member is composed of the coated magnetic particles prepared above, a nonmagnetic conductive sleeve for supporting the coated magnetic particles, and a magnet roll included therein, and the coated magnetic particles are formed on the sleeve with a thickness. Coating was performed at 1 mm to form a charging nip having a width of about 5 mm between the photosensitive member and the photosensitive member. The gap between the magnetic particle holding sleeve and the photosensitive member was about 500 μm. Further, the magnet roll is rotated so that the sleeve surface rubs in the opposite direction at twice as fast as the peripheral speed of the surface of the photoconductor, and the photoconductor and the magnetic brush are in uniform contact with each other. I did it.

(Development process, development means)
In developing the latent image on the photoreceptor in the present invention, it is preferable to apply an alternating electric field. In the developing device (600) shown in FIG. 3, during development, a vibration bias voltage in which an AC voltage is superimposed on a DC voltage is applied to the developing sleeve (601) as a developing bias by a power source (602). The background portion potential and the image portion potential are located between the maximum value and the minimum value of the vibration bias potential. As a result, an alternating electric field whose direction changes alternately is formed in the developing portion (603). In this alternating electric field, the developer toner and the carrier vibrate vigorously, and the toner (605) flies to the photosensitive member (604) by shaking off the electrostatic binding force to the developing sleeve (601) and the carrier. It adheres corresponding to the latent image. The toner (605) is a toner manufactured by the above-described manufacturing method of the present invention.

  The difference (maximum peak voltage) between the maximum value and the minimum value of the vibration bias voltage is preferably 0.5 to 5 kV, and the frequency is preferably 1 to 10 kHz. As the waveform of the vibration bias voltage, a rectangular wave, a sine wave, a triangular wave or the like can be used. As described above, the DC voltage component of the vibration bias is a value between the background part potential and the image part potential, but the value closer to the background part potential than the image part potential is more likely to cover the background part potential region. This is preferable for preventing toner adhesion.

  When the vibration bias voltage waveform is a rectangular wave, the duty ratio is preferably 50% or less. Here, the duty ratio is a ratio of time during which the toner is directed to the photosensitive member during one period of the vibration bias. By doing so, the difference between the peak value at which the toner is directed to the photoreceptor and the time average value of the bias can be increased, so that the movement of the toner is further activated and the potential of the latent image surface is increased. It can adhere to the distribution and improve the roughness and resolution. In addition, since the difference between the peak value of the carrier having a charge opposite to that of the toner and the time average value of the bias toward the photosensitive member can be reduced, the movement of the carrier is reduced, and the background portion of the latent image is reduced. The probability of carriers adhering to the substrate can be greatly reduced.

(Fixing device)
As the fixing device used in the image forming method of the present invention, for example, the fixing device shown in FIG. 4 can be used. The fixing device shown in FIG. 4 includes a heating roller (710) heated by electromagnetic induction of the induction heating means (760), a fixing roller (720) (opposite rotating body) arranged in parallel with the heating roller (710). And an endless belt-like fixing belt that is stretched between a heating roller (710) and a fixing roller (720), heated by the heating roller (710), and rotated in the direction of arrow A by at least rotation of any of these rollers. A heat-resistant belt (toner heating medium) (730) and a pressure roller (740) that is pressed against the fixing roller (720) via the fixing belt (730) and rotates in the forward direction with respect to the fixing belt (730). (Pressure rotator).

The heating roller (710) is made of, for example, a hollow cylindrical magnetic metal member such as iron, cobalt, nickel, or an alloy of these metals, and has an outer diameter of, for example, 20 to 40 mm and a thickness of, for example, 0.3 to 1.0 mm. It has a low heat capacity and quick temperature rise.
The fixing roller (720) (opposite rotating body) is made of, for example, a metal core (721) made of stainless steel or the like and a heat-resistant silicone rubber that is solid or foamed and covered with the core (721). It consists of a member (722). In order to form a contact portion having a predetermined width between the pressure roller (740) and the fixing roller (720) by the pressing force from the pressure roller (740), the outer shape is set to about 20 to 40 mm. 710). The elastic member (722) has a thickness of about 4 to 6 mm. With this configuration, since the heat capacity of the heating roller (710) is smaller than the heat capacity of the fixing roller (720), the heating roller (710) is rapidly heated and the warm-up time is shortened.

  The fixing belt (730) stretched between the heating roller (710) and the fixing roller (720) is heated at the contact portion (W1) with the heating roller (710) heated by the induction heating means (760). . Then, the inner surface of the fixing belt (730) is continuously heated by the rotation of the heating roller (710) and the fixing roller (720). As a result, the entire belt is heated.

FIG. 5 shows a layer structure of the fixing belt (730). The belt (730) has the following four layers from the inner layer to the surface layer, and can be configured as follows.
-Substrate (731): Resin layer such as polyimide (PI) resin-Heat generation layer (732): Conductive material layer such as Ni, Ag, SUS-Intermediate layer (733): Elastic layer for uniform fixing-Release layer (734): Resin layer such as fluorine resin material for releasing effect and oil-less

  The thickness of the release layer (734) is preferably about 10 μm to 300 μm, particularly about 200 μm. In this way, in the fixing device (700) as shown in FIG. 4, the toner image (T) formed on the recording material (770) is sufficiently wrapped by the surface layer portion of the fixing belt (730). The image (T) can be heated and melted uniformly. The thickness of the release layer (734), that is, the surface release layer, needs to be at least 10 μm in order to ensure wear resistance over time. Further, when the thickness of the release layer (734) is larger than 300 μm, the heat capacity of the fixing belt (730) is increased and the time required for warm-up is increased. Further, the surface temperature of the fixing belt (730) is hardly lowered in the toner image fixing step, and the effect of aggregating the melted toner at the fixing portion outlet cannot be obtained, and the releasability of the fixing belt (730) is lowered. The toner of the toner image (T) adheres to the fixing belt (730), and so-called hot offset occurs. The heat generating layer (732) made of the above metal may be used as the base of the fixing belt (730), but the heat resistance of fluorine resin, polyimide resin, polyamide resin, polyamideimide resin, PEEK resin, PES resin, PPS resin, etc. A resin layer having properties may be used.

  The pressure roller (740) includes, for example, a metal core (741) made of a metal cylindrical member having a high thermal conductivity such as copper or aluminum, and heat resistance and toner separation provided on the surface of the metal core (741). It is comprised from the elastic member (742) with high moldability. In addition to the above metal, SUS may be used for the core metal (741). The pressure roller (740) presses the fixing roller (720) via the fixing belt (730) to form a fixing nip (N). In this embodiment, the pressure roller (740) By making the hardness harder than that of the fixing roller (720), the pressure roller (740) bites into the fixing roller (720) (and the fixing belt (730)), and by this biting, the recording material (770) becomes. The recording material (770) is easily separated from the surface of the fixing belt (730) because it follows the circumferential shape of the surface of the pressure roller (740). The outer diameter of the pressure roller (740) is about 20 to 40 mm, which is the same as that of the fixing roller (720), but the wall pressure is about 0.5 to 2.0 mm and is thinner than the fixing roller (720).

  As shown in FIG. 4, the induction heating means (760) for heating the heating roller (710) by electromagnetic induction includes an excitation coil (761) as a magnetic field generation means and a coil around which the excitation coil (761) is wound. And a guide plate (762). The coil guide plate (762) has a semi-cylindrical shape disposed close to the outer peripheral surface of the heating roller (710), and the excitation coil (761) has a single long excitation coil wire as the coil guide plate (762). Along the axial direction of the heating roller (710). The excitation coil (761) has an oscillation circuit connected to a drive power supply (not shown) whose frequency is variable. On the outside of the exciting coil (761), a semi-cylindrical exciting coil core (763) made of a ferromagnetic material such as ferrite is fixed to the exciting coil core support member (764) and is disposed close to the exciting coil (761). Yes.

[Process cartridge]
The process cartridge of the present invention includes an electrophotographic photosensitive member, a charging unit that charges the electrophotographic photosensitive member, an exposure unit that forms an electrostatic latent image on the charged electrophotographic photosensitive member, and the electrophotographic photosensitive member. Developing means for converting the electrostatic latent image formed on the body into a toner image with toner, and transferring the toner image formed on the electrophotographic photosensitive member onto a recording material with or without an intermediate transfer member. A transfer unit; a fixing unit that fixes the toner image transferred onto the recording material onto the recording material by a heat and pressure fixing member; and a toner image that has been transferred onto the intermediate transfer member or the recording material by the transfer unit. Among the means in the image forming apparatus provided with the cleaning means for cleaning the transfer residual toner adhering to the surface of the electrophotographic photosensitive member, the above means including at least the electrophotographic photosensitive member and the developing means. Supporting the body is obtained by detachable to the image forming apparatus main body. The developing means includes a toner manufactured by the above-described manufacturing method of the present invention. As the developing unit and the charging unit, the above-described developing device and charging device can be preferably used.

  An example of the process cartridge of the present invention is shown in FIG. The process cartridge (800) shown in FIG. 6 includes a photoreceptor (801), a charging unit (802), a developing unit (803), and a cleaning unit (806). The operation of the process cartridge (800) will be described. The photosensitive member (801) is rotationally driven at a predetermined peripheral speed. In the rotating process, the photosensitive member (801) is uniformly charged at a predetermined positive or negative potential on its peripheral surface by the charging means (802), and then from an image exposure means (not shown) such as slit exposure or laser beam scanning exposure. In this way, an electrostatic latent image is sequentially formed on the peripheral surface of the photoreceptor (801), and the formed electrostatic latent image is then converted into a toner image by the developing means (803) and developed. The toner image is sequentially transferred from the paper feeding unit to the recording material fed between the photosensitive member (801) and a transfer unit (not shown) in synchronization with the rotation of the photosensitive member (801) by the transfer unit. . The recording material that has undergone image transfer is separated from the surface of the photosensitive member, introduced into an image fixing means (not shown), and fixed on the image, and printed out as a copy (copy). The surface of the photoconductor (801) after the image transfer is cleaned by removing the transfer residual toner by the cleaning means (806), and after being further discharged, it is repeatedly used for image formation.

(Full-color image forming method, image forming apparatus example)
As the full-color image forming apparatus used in the full-color image forming method of the present invention, for example, the tandem image forming apparatus (100) shown in FIGS. 7 and 8 can be used.
In FIG. 7, an image forming apparatus (100) includes an image writing unit (120Bk, 120C, 120M, 120Y), an image forming unit (130Bk, 130C, 130M, 130Y), a supply for performing color image formation by electrophotography. It is mainly composed of a paper portion (140). Based on the image signal, image processing is performed by an image processing unit (not shown), and converted into black (Bk), cyan (C), magenta (M), and yellow (Y) color signals for image formation, It transmits to an image writing part (120Bk, 120C, 120M, 120Y). The image writing unit (120Bk, 120C, 120M, 120Y) is, for example, a laser scanning optical system including a laser light source, a deflector such as a rotary polygon mirror, a scanning imaging optical system, and a mirror group (none of which are shown). Yes, it has four writing optical paths corresponding to the respective color signals, and performs image writing corresponding to the respective color signals to the image forming units (130Bk, 130C, 130M, 130Y).

  The image forming unit (130Bk, 130C, 130M, 130Y) includes photoconductors (210Bk, 210C, 210M, 210Y) for black, cyan, magenta, and yellow, and photoconductors (210Bk, 210C, 210M and 210Y) are usually OPC photoreceptors. Around each of the photoconductors (210Bk, 210C, 210M, 210Y), there are charging devices (215Bk, 215C, 215M, 215Y), and laser light exposure units from the image writing unit (120Bk, 120C, 120M, 120Y). , Developing devices for respective colors (200Bk, 200C, 200M, 200Y), primary transfer devices (230Bk, 230C, 230M, 230Y), cleaning devices (300Bk, 300C, 300M, 300Y), static eliminators (not shown), etc. Is arranged. The developing device (200Bk, 200C, 200M, 200Y) uses a two-component magnetic brush developing system. An intermediate transfer belt (220) is interposed between each photoconductor (210Bk, 210C, 210M, 210Y) and the primary transfer device (230Bk, 230C, 230M, 230Y), and the intermediate transfer belt (220). The toner images of the respective colors are sequentially transferred from the respective photoconductors so as to carry the toner images on the respective photoconductors.

  In some cases, a pre-transfer charger as a pre-transfer charging unit is disposed outside the intermediate transfer belt (220) at a position after passing through the primary transfer position of the final color and before passing through the secondary transfer position. preferable. This pre-transfer charger converts the toner image into a toner image before transferring the toner image on the intermediate transfer belt (220) transferred to the photosensitive member (210) in the primary transfer portion onto a transfer sheet as a recording material. It is uniformly charged to the same polarity.

  The toner image on the intermediate transfer belt (220) transferred from each photoconductor (210Bk, 210C, 210M, 210Y) includes a halftone portion and a solid portion, or includes a portion where the amount of toner overlap is different. Therefore, the charge amount may vary. Further, when the discharge amount generated in the gap adjacent to the downstream side of the primary transfer portion in the movement direction of the intermediate transfer belt causes variation in charge amount in the toner image on the intermediate transfer belt (220) after the primary transfer. There is also. Such variation in the charge amount in the same toner image lowers the transfer margin in the secondary transfer portion that transfers the toner image on the intermediate transfer belt (220) onto the transfer paper. Therefore, the toner image before being transferred to the transfer paper by the pre-transfer charger is uniformly charged to the same polarity as the toner image, thereby eliminating the variation in the charge amount in the same toner image and the transfer margin in the secondary transfer portion. Has improved.

  As described above, according to this image forming method, the toner image on the intermediate transfer belt (220) transferred from each photoconductor (210Bk, 210C, 210M, 210Y) is uniformly charged by the pre-transfer charger, so that the intermediate transfer is performed. Even if there is a variation in the charge amount in the toner image on the belt (220), the transfer characteristics in the secondary transfer portion can be made almost constant across the portions of the toner image on the intermediate transfer belt (220). . Therefore, it is possible to suppress a decrease in transfer margin when transferring to transfer paper and to stably transfer a toner image.

  In this image forming method, the amount of charge charged by the pre-transfer charger varies depending on the moving speed of the intermediate transfer belt (220) that is the object to be charged. For example, if the moving speed of the intermediate transfer belt (220) is slow, the time for the same portion of the toner image on the intermediate transfer belt (220) to pass through the charging area by the pre-transfer charger becomes long, and the charge amount increases. Conversely, when the moving speed of the intermediate transfer belt (220) is fast, the charge amount of the toner image on the intermediate transfer belt (220) becomes small. Therefore, when the moving speed of the intermediate transfer belt (220) changes while the toner image on the intermediate transfer belt (220) passes through the charging position by the pre-transfer charger, the intermediate transfer belt (220 It is desirable to control the pre-transfer charger so that the charge amount with respect to the toner image does not change in the middle according to the movement speed of ().

  Conductive rollers (241), (242), and (243) are provided between the primary transfer devices (230Bk, 230C, 230M, and 230Y). The transfer paper is fed from the paper feed unit (140) and then carried on the transfer belt (180) via the registration roller pair (160), so that the intermediate transfer belt (220) and the transfer belt (180) are in contact with each other. The toner image on the intermediate transfer belt (220) is transferred to the transfer paper by the secondary transfer roller (170), and a color image is formed.

  Then, the transfer paper after image formation is conveyed to the fixing device (150) by the secondary transfer belt (180), and the image is fixed to obtain a color image. The toner on the intermediate transfer belt (220) remaining without being transferred is removed from the belt by an intermediate transfer belt cleaning device (not shown).

  Since the toner polarity on the intermediate transfer belt (220) before transfer onto the transfer paper is the same negative polarity as that during development, a positive transfer bias voltage is applied to the secondary transfer roller (170), and the toner is transferred. It is transferred onto paper. The nip pressure at this portion affects the transfer property and greatly affects the fixability. Further, the toner on the intermediate transfer belt (220) remaining without being transferred is discharged and charged to the positive polarity side and charged from 0 to the positive side at the moment when the transfer paper and the intermediate transfer belt (220) are separated. Note that the toner image formed when the transfer paper is jammed or in the non-image area is not affected by the secondary transfer, and of course remains in the negative polarity.

  The thickness of the photosensitive layer is 30 μm, the beam spot diameter of the optical system is 50 × 60 μm, and the light quantity is 0.47 mW. The developing process is carried out with the charging (exposure side) potential V0 of the photoconductor (black) (210Bk) set to -700V, the post-exposure potential VL set to -120V, and the developing bias voltage set to -470V, ie, the developing potential 350V. The visible image of the toner (black) formed on the photoconductor (black) (210Bk) is then transferred (intermediate transfer belt and transfer paper) and completed as an image through a fixing process. First, all colors are transferred from the primary transfer device (230Bk, 230C, 230M, 230Y) to the intermediate transfer belt (220), and then applied to a transfer sheet by applying a bias to another secondary transfer roller (170). Transcribed.

  Next, the photoconductor cleaning device will be described in detail. In FIG. 7, each developing device (200Bk, 200C, 200M, 200Y) and each cleaning device (300Bk, 300C, 300M, 300Y) are connected to each other by a toner transfer pipe (250Bk, 250C, 250M, 250Y). (Dashed line in FIG. 7). Each toner transfer pipe (250Bk, 250C, 250M, 250Y) contains a screw (not shown), and the toner collected by each cleaning device (300Bk, 300C, 300M, 300Y) Each developing device (200Bk, 200C, 200M, 200Y) is transferred.

  In the conventional direct transfer method using the combination of the four photosensitive drums and the belt conveyance, paper dust adheres when the photoreceptor and the transfer paper come into contact with each other, and the paper dust is contained when the toner is collected. The image was deteriorated such as toner missing and could not be used. Furthermore, in the conventional system combining a single photoconductor drum and intermediate transfer, the use of an intermediate transfer member eliminates paper dust adhesion to the photoconductor during transfer paper transfer, but recycling of residual toner on the photoconductor In practice, it is practically impossible to separate the mixed color toners. There is also a proposal to use a mixed color toner as a black toner, but even if all the colors are mixed, it does not become black, and the color changes depending on the print mode. Therefore, it is impossible to recycle the toner with one photoconductor configuration.

  On the other hand, in this full-color image forming apparatus, since the intermediate transfer belt (220) is used, paper dust is hardly mixed, and adhesion of paper dust to the intermediate transfer belt (220) during paper transfer is prevented. The Since each photoconductor (210Bk, 210C, 210M, 210Y) uses independent color toner, it is not necessary to contact or separate each photoconductor cleaning device (300Bk, 300C, 300M, 300Y), and only the toner is reliably collected. can do.

  The positively charged toner remaining on the intermediate transfer belt (220) is cleaned by a conductive fur brush (262) to which a negative voltage is applied. The method of applying a voltage to the conductive fur brush (262) is exactly the same as that of the conductive fur brush (261) except for the polarity. The toner remaining without being transferred is also almost cleaned by the two conductive fur brushes (261) and (262). Here, toner, paper powder, talc, and the like remaining without being cleaned by the conductive fur brush (262) are negatively charged by the negative voltage of the conductive fur brush (262). The next black primary transfer is a transfer using a positive voltage, and negatively charged toner or the like is attracted to the intermediate transfer belt (220) side, so that the transfer to the photoconductor (black) (210Bk) side can be prevented.

  Next, the intermediate transfer belt (220) used in this image forming apparatus will be described. As described above, the intermediate transfer belt is preferably a single resin layer, but may have an elastic layer or a surface layer as necessary.

  As the resin material constituting the resin layer, polycarbonate, fluororesin (ETFE, PVDF), polystyrene, chloropolystyrene, poly-α-methylstyrene, styrene-butadiene copolymer, styrene-vinyl chloride copolymer, styrene -Vinyl acetate copolymer, styrene-maleic acid copolymer, styrene-acrylic acid ester copolymer (styrene-methyl acrylate copolymer, styrene-ethyl acrylate copolymer, styrene-butyl acrylate copolymer) Styrene-octyl acrylate copolymer and styrene-phenyl acrylate copolymer), styrene-methacrylic acid ester copolymer (styrene-methyl methacrylate copolymer, styrene-ethyl methacrylate copolymer, styrene- (Methacrylic acid phenyl copolymer, etc.), styrene -Styrenic resins (monopolymer or copolymer containing styrene or a styrene-substituted product) such as methyl α-chloroacrylate copolymer, styrene-acrylonitrile-acrylic acid ester copolymer, methyl methacrylate resin, methacrylic acid Butyl resin, ethyl acrylate resin, butyl acrylate resin, modified acrylic resin (silicone modified acrylic resin, vinyl chloride resin modified acrylic resin, acrylic / urethane resin, etc.), vinyl chloride resin, styrene-vinyl acetate copolymer, vinyl chloride -Vinyl acetate copolymer, rosin modified maleic acid resin, phenol resin, epoxy resin, polyester resin, polyester polyurethane resin, polyethylene, polypropylene, polybutadiene, polyvinylidene chloride, ionomer resin, polyurethane resin, silicone resin , Ketone resin, ethylene - ethyl acrylate copolymer, may be used xylene resin and polyvinyl butyral resin, polyamide resin, one kind or two kinds or more selected from the group consisting of modified polyphenylene oxide resin. However, it is a matter of course that the material is not limited to the above materials.

  Examples of the elastic material (elastic material rubber, elastomer) constituting the elastic layer include butyl rubber, fluorine-based rubber, acrylic rubber, EPDM, NBR, acrylonitrile-butadiene-styrene rubber natural rubber, isoprene rubber, styrene-butadiene rubber, Butadiene rubber, ethylene-propylene rubber, ethylene-propylene terpolymer, chloroprene rubber, chlorosulfonated polyethylene, chlorinated polyethylene, urethane rubber, syndiotactic 1,2-polybutadiene, epichlorohydrin rubber, ricone rubber, fluororubber, Polysulfide rubber, polynorbornene rubber, hydrogenated nitrile rubber, thermoplastic elastomer (eg polystyrene, polyolefin, polyvinyl chloride, polyurethane, polyamide, polyurea, polyester) It is possible to use one kind or two kinds or more selected from the group consisting of fluorocarbon resin) or the like. However, it is a matter of course that the material is not limited to the above materials.

  The material for the surface layer is not particularly limited, but a material that reduces the adhesive force of the toner to the surface of the intermediate transfer belt and increases the secondary transfer property is required. For example, materials that use one or more of polyurethane, polyester, epoxy resin, etc. to reduce surface energy and increase lubricity, such as fluorine resin, fluorine compound, fluorocarbon, titanium dioxide, silicon carbide, etc. One kind or two or more kinds of powders and particles or particles having different particle diameters can be dispersed and used. Further, it is also possible to use a material having a surface energy reduced by forming a fluorine-rich layer on the surface by heat treatment, such as a fluorine-based rubber material.

  A resistance value adjusting conductive agent is added to the resin layer and the elastic layer. The conductive agent for adjusting the resistance value is not particularly limited. For example, carbon black, graphite, metal powder such as aluminum and nickel, tin oxide, titanium oxide, antimony oxide, indium oxide, potassium titanate, antimony oxide-tin oxide Conductive metal oxides such as composite oxide (ATO) and indium oxide-tin oxide composite oxide (ITO), and conductive metal oxide covered with insulating fine particles such as barium sulfate, magnesium silicate, and calcium carbonate. It may be a thing. Of course, the conductive agent is not limited thereto.

  FIG. 8 shows another example of an image forming apparatus used in the image forming method of the present invention, which is a copying apparatus (100) provided with a tandem indirect transfer type electrophotographic image forming apparatus. In FIG. 8, (110) is a copying apparatus main body, (200) is a paper feed table on which it is placed, (300) is a scanner mounted on the copying apparatus main body (110), and (400) is an automatic document feeder mounted thereon. Device (ADF). The copying machine main body (110) is provided with an endless belt-shaped intermediate transfer member (10) in the center.

  Then, as shown in FIG. 8, in this example, the three support rollers (14), (15), and (16) are hung to enable rotation and conveyance in the clockwise direction in the figure. In this illustrated example, an intermediate transfer body cleaning device (17) for removing residual toner remaining on the intermediate transfer body (10) after image transfer is provided on the left of the second support roller (15) among the three. Further, among the three, the intermediate transfer member (10) stretched between the first support roller (14) and the second support roller (15) has yellow, cyan and magenta along the transport direction. The black image forming means (18) are arranged side by side to constitute a tandem image forming apparatus (120).

  An exposure device (21) is further provided on the tandem image forming apparatus (120) as shown in FIG. On the other hand, a secondary transfer device (22) is provided on the side opposite to the tandem image forming device (120) with the intermediate transfer member (10) interposed therebetween. In the illustrated example, the secondary transfer device (22) includes a secondary transfer belt (24), which is an endless belt, spanned between two rollers (23), and the second transfer device (22) passes through an intermediate transfer member (10). 3 is pressed against the support roller (16), and the image on the intermediate transfer body (10) is transferred to the sheet. Next to the secondary transfer device (22), a fixing device (25) for fixing the transferred image on the sheet is provided. The fixing device (25) is configured by pressing a pressure roller (27) against a fixing belt (26) which is an endless belt. The secondary transfer device (22) described above is also provided with a sheet transport function for transporting the image-transferred sheet to the fixing device (25). Of course, as the secondary transfer device (22), a transfer roller or a non-contact charger may be arranged. In such a case, it is difficult to provide this sheet conveying function together. In the illustrated example, a sheet is placed under such a secondary transfer device (22) and a fixing device (25) to record an image on both sides of the sheet in parallel with the tandem image forming device (120). A sheet inverting device (28) for inverting is provided.

  Now, when making a copy using this color electrophotographic apparatus, the document is set on the document table (130) of the automatic document feeder (400). Alternatively, the automatic document feeder (400) is opened, a document is set on the contact glass (32) of the scanner (300), and the automatic document feeder (400) is closed and pressed by it.

  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 other contact glass (32). When a document is set on the scanner, the scanner (300) is immediately driven to travel on the first traveling body (33) and the second traveling body (34). Then, the first traveling body (33) emits light from the light source, and the reflected light from the document surface is further reflected toward the second traveling body (34) and reflected by the mirror of the second traveling body (34). Then, the image is placed in the reading sensor (36) through the imaging lens (35) and the content of the original is read.

  When a start switch (not shown) is pressed, one of the support rollers (14), (15), and (16) is driven to rotate by the drive motor (not shown), and the other two support rollers are driven to rotate. The transfer body (10) is rotated and conveyed. At the same time, the individual image forming means (18) rotates the photoconductor to form black, yellow, magenta, and cyan monochrome images on each photoconductor. Then, along with the conveyance of the intermediate transfer member (10), these monochrome images are sequentially transferred to form a composite color image on the intermediate transfer member (10).

  On the other hand, when a start switch (not shown) is pressed, one of the paper feed rollers (142) of the paper feed table (200) is selectively rotated, and one of paper feed cassettes (144) provided in multiple stages in the paper bank (143). The sheet is fed out from the sheet, separated one by one by a separation roller (145), put into a sheet feeding path (146), and conveyed by a conveying roller (147) to a sheet feeding path (148) in the copying machine main body (100). Guide and stop against the registration roller (49).

  Alternatively, the sheet feeding roller (50) is rotated to feed out the sheets on the manual feed tray (51), separated one by one by the separation roller (58), and put into the manual sheet feeding path (53). ) And stop.

  Then, the registration roller (49) is rotated in time with the composite color image on the intermediate transfer member (10), and the sheet is fed between the intermediate transfer member (10) and the secondary transfer device (22). The image is transferred by the next transfer device (22) and a color image is recorded on the sheet.

  The sheet after the image transfer is conveyed by the secondary transfer device (22) and sent to the fixing device (25). The fixing device (25) applies heat and pressure to fix the transferred image, and then the switching claw. It is switched at (55), discharged by the discharge roller (56), and stacked on the discharge tray (57). Alternatively, it is switched by the switching claw (55) and put into the sheet reversing device (28), where it is reversed and guided again to the transfer position, and an image is recorded also on the back surface, and then the paper discharge tray (56) is discharged by the discharge roller (56). 57) Drain up.

  On the other hand, the intermediate transfer body (10) after the image transfer is removed by the intermediate transfer body cleaning device (17) to remove residual toner remaining on the intermediate transfer body (10) after the image transfer, and the tandem image forming apparatus (120). To prepare for image formation again. Here, the registration roller (49) is generally used while being grounded, but it is also possible to apply a bias for removing paper dust from the sheet.

  Hereinafter, the present invention will be described in more detail by way of examples, but the present invention is not limited thereto. In addition, a part refers to a weight part.

(Synthesis of organic fine particle emulsion)
In a reaction vessel equipped with a stir bar and a thermometer, 683 parts of water, 11 parts of sodium salt of ethylene oxide methacrylate adduct sulfate (Eleminol RS-30: manufactured by Sanyo Chemical Industries), 138 parts of styrene, 138 parts of methacrylic acid, When 1 part of ammonium persulfate was added and stirred at 400 rpm for 15 minutes, a white emulsion was obtained. The system was heated to raise the system temperature to 75 ° C. and reacted for 5 hours. Further, 30 parts of a 1% ammonium persulfate aqueous solution was added, and the mixture was aged at 75 ° C. for 5 hours, and an aqueous dispersion of a vinyl resin (a copolymer of styrene-methacrylic acid-methacrylic acid ethylene oxide adduct sulfate sodium salt) [fine particles Dispersion] was obtained.
The volume average particle diameter of the [fine particle dispersion] measured by LA-920 was 0.14 μm.

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

[Synthesis of low molecular weight polyester]
(Synthesis of low molecular weight polyester 1)
In a reaction vessel equipped with a condenser, a stirrer and a nitrogen introduction tube, 781 parts of bisphenol A propylene oxide 3 mol adduct, 218 parts of terephthalic acid, 48 parts of adipic acid and 2 parts of dibutyltin oxide were placed at an ordinary pressure of 230 ° C. The reaction was continued for 8 hours at a reduced pressure of 10 to 15 mmHg, and 45 parts of trimellitic anhydride was added to the reaction vessel and reacted at 180 ° C. for 2 hours at normal pressure. Obtained.
[Low molecular polyester 1] had a number average molecular weight of 2500, a weight average molecular weight of 6700, Tg of 43 ° C., an acid value of 25, a resin softening coefficient of 0.166, G ′ (Tfb) = 9800, and an SP value of 11.0.

(Synthesis of low molecular weight polyester 2)
Next, [Low molecular polyester 2] was obtained in the same manner as [Low molecular polyester 1] except that the monomer ratio was adjusted so that the SP value was 12.1.
[Low molecular polyester 2] had a number average molecular weight of 2700, a weight average molecular weight of 6900, a Tg of 45 ° C., and an acid value of 23.

(Synthesis of low molecular weight polyester 3)
Next, [Low molecular polyester 3] was obtained in the same manner as [Low molecular polyester 1] except that the monomer ratio was adjusted so that the SP value was 9.9.
[Low molecular polyester 3] had a number average molecular weight of 2,400, a weight average molecular weight of 6,300, a Tg of 43 ° C., and an acid value of 26.

[Synthesis of crystalline polyester]
Equipped with 1260g of 1,6-butanediol, 120g of ethylene glycol, 1400g of fumaric acid, 350g of trimellitic anhydride, 3.5g of tin octylate and 1.5g of hydroquinone, equipped with nitrogen introduction tube, dehydration tube, stirrer and thermocouple The reaction was carried out at 160 ° C. for 5 hours, heated to 200 ° C. for 1 hour, further reacted at 8.3 kPa for 1 hour, [Crystalline Polyester 1 ] Was obtained.
[Crystalline polyester 1] had a melting point of 89 ° C.

[Synthesis of Prepolymer Precursor (Intermediate Polyester)]
(Synthesis of Intermediate Polyester 1)
In a reaction vessel equipped with a cooling pipe, a stirrer and a nitrogen introduction pipe, 711 parts of bisphenol A ethylene oxide 2 mol adduct, 84 parts of bisphenol A propylene oxide 2 mol adduct, 295 parts terephthalic acid, trimellitic anhydride 23 And 2 parts of dibutyltin oxide were added, reacted at 230 ° C. under normal pressure for 8 hours, and further reacted for 5 hours at a reduced pressure of 10 to 15 mmHg to obtain [Intermediate Polyester 1].
[Intermediate Polyester 1] had a number average molecular weight Mn of 6940, a weight average molecular weight of Mw 29200, a peak top molecular weight Mpt of 18600, an Mw / Mn of 4.2, a Tg of 45 ° C., an acid value of 0.5, and a hydroxyl value of 49.

(Synthesis of Intermediate Polyester 2)
Next, [Intermediate Polyester 2] was obtained in the same manner as [Intermediate Polyester 1] except that the reaction time was 5 hours at a normal pressure of 230 ° C.
[Intermediate Polyester 2] had a number average molecular weight of 4940 and a weight average molecular weight of 17,300. The peak top molecular weight Mpt is shown in Table 1.

(Synthesis of Intermediate Polyester 3)
Next, [Intermediate polyester 3] was obtained in the same manner as [Intermediate polyester 1] except that the reaction time was 11 hours at 230 ° C. under normal pressure.
[Intermediate Polyester 3] had a number average molecular weight of 7130 and a weight average molecular weight of 32100. The peak top molecular weight Mpt is shown in Table 1.

(Synthesis of Intermediate Polyester 4)
Next, [Intermediate polyester 4] was obtained in the same manner as [Intermediate polyester 1] except that the reaction time was 10 minutes at a normal pressure of 250 ° C.
[Intermediate Polyester 4] had a number average molecular weight of 8020 and a weight average molecular weight of 30500. The peak top molecular weight Mpt is shown in Table 1.

(Synthesis of Intermediate Polyester 5)
Next, [Intermediate polyester 5] was obtained in the same manner as [Intermediate polyester 1], except that the reaction time was 4 hours at a normal pressure of 230 ° C.
[Intermediate Polyester 5] had a number average molecular weight of 4860 and a weight average molecular weight of 13600. The peak top molecular weight Mpt is shown in Table 1.

(Synthesis of Intermediate Polyester 6)
Next, [Intermediate polyester 6] was obtained in the same manner as [Intermediate polyester 1] except that the reaction time was 13 hours at a normal pressure of 230 ° C.
[Intermediate Polyester 6] had a number average molecular weight of 5930 and a weight average molecular weight of 36,200. The peak top molecular weight Mpt is shown in Table 1.

(Synthesis of Intermediate Polyester 7)
Next, [Intermediate Polyester 7] was obtained in the same manner as [Intermediate Polyester 1] except that propylene glycol was used as the alcohol monomer and the reaction time was 7 hours at a normal pressure of 230 ° C.
[Intermediate Polyester 7] had a number average molecular weight of 7160 and a weight average molecular weight of 30800. The peak top molecular weight Mpt is shown in Table 1.

[Prepolymer synthesis]
(Synthesis of Prepolymer 1)
Next, 411 parts of [Intermediate polyester 1], 89 parts of isophorone diisocyanate, and 500 parts of ethyl acetate are placed in a reaction vessel equipped with a cooling tube, a stirrer and a nitrogen introduction tube, and reacted at 100 ° C. for 5 hours. Polymer 1] was obtained.
[Prepolymer 1] had an average number of isocyanate groups of 2.0.

(Synthesis of Prepolymer 2)
Next, [Prepolymer 2] was obtained in the same manner as [Prepolymer 1] except that the intermediate polyester 2 was used so that the average number of isocyanate groups of the produced prepolymer was 2.0.

(Synthesis of Prepolymer 3)
Next, [Prepolymer 3] was obtained in the same manner as [Prepolymer 1] except that the intermediate polyester 3 was used so that the average number of isocyanate groups of the produced prepolymer was 2.0.

(Synthesis of Prepolymer 4)
Next, [Prepolymer 4] was obtained in the same manner as [Prepolymer 1] except that the intermediate polyester 4 was used so that the average number of isocyanate groups of the produced prepolymer was 2.0.

(Synthesis of Prepolymer 5)
Next, [Prepolymer 5] was obtained in the same manner as [Prepolymer 1] except that the intermediate polyester 5 was used so that the average number of isocyanate groups of the produced prepolymer was 2.0.

(Synthesis of Prepolymer 6)
Next, [Prepolymer 6] was obtained in the same manner as [Prepolymer 1] except that the intermediate polyester 6 was used so that the average number of isocyanate groups in the produced prepolymer was 2.0.

(Synthesis of Prepolymer 7)
Next, [Prepolymer 7] was obtained in the same manner as [Prepolymer 1] except that the intermediate polyester 7 was used so that the average number of isocyanate groups of the produced prepolymer was 2.0.

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

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

[Example 1]
(Creation of oil phase A)
A container equipped with a stir bar and a thermometer was charged with 378 parts of [low molecular weight polyester 1], 947 parts of ethyl acetate, and 32 parts of monoester wax 1 (melting point 71 ° C., SP value 16.5, kinematic viscosity 8.2). The mixture was heated to 80 ° C. with stirring, held at 80 ° C. for 5 hours, cooled to 30 ° C. over 1 hour, and then added with 220 parts of [Crystalline Polyester 1] and stirred [Raw Material Solution 1] Got.

  Then, 1324 parts of the raw material solution 1 was transferred to a container, and using a bead mill (Ultra Visco Mill, manufactured by Imex Co., Ltd.), a liquid feeding speed of 1 kg / hr, a disk peripheral speed of 6 m / sec, and a volume of 0.5 mm zirconia beads of 80 volumes [Raw material dispersion 1] was prepared under the conditions of% filling and 3 passes.

Next, “Master Batch 1” was added to [Raw Material Dispersion 1], and one pass was performed with a bead mill under the above conditions to obtain [Oil Phase Dispersion A].
The solid content concentration of [Oil Phase Dispersion A] (130 ° C., 30 minutes) was 50%.

(Emulsification 1)
[Oil Phase Dispersion A] 648 parts, [Prepolymer 1] 154 parts, [Ketimine Compound 1] 6.6 parts in a container and mixed for 1 minute at 5,000 rpm with a TK homomixer (manufactured by Tokushu Kika) After that, 1200 parts of [Aqueous phase 1] was added to the container, and mixed with a TK homomixer at 13,000 rpm for 3 minutes to obtain [Emulsified slurry A].

(Emulsification 2)
In [Emulsified slurry A], 648 parts of [Oil phase dispersion B], 154 parts of [Prepolymer 1], and 6.6 parts of [Ketimine compound 1] are put in a container, and TK homomixer (manufactured by Tokushu Kika) Was mixed at 5,000 rpm for 1 minute, and then mixed with a TK homomixer at 13,000 rpm for 3 minutes to obtain [Emulsified slurry A + B].

(Atypical → Solvent removal)
[Emulsified slurry A + B] was put into a container equipped with a stirrer and a thermometer, allowed to stand at 15 ° C. for 1 hour, and then desolvated at 30 ° C. for 1 hour to obtain [Dispersed slurry 1].
[Dispersion Slurry 1] had a volume average particle size of 5.52 μm and a number average particle size of 4.74 μm (measured with Multisizer II).

(Washing → drying)
[Dispersion Slurry 1] After filtering 100 parts under reduced pressure,
[1]: 100 parts of ion-exchanged water was added to the filter cake, mixed with a TK homomixer (rotation speed: 12,000 rpm for 10 minutes), and then filtered.
[2]: 100 parts of 10% aqueous sodium hydroxide solution was added to the filter cake of [1], ultrasonic vibration was applied and mixed with a TK homomixer (30 minutes at 12,000 rpm), and then filtered under reduced pressure. .
This ultrasonic alkali cleaning was performed again (two ultrasonic alkali cleanings).
[3]: 100 parts of 10% hydrochloric acid was added to the filter cake of [2], mixed with a TK homomixer (10 minutes at 12,000 rpm), and then filtered.
[4]: Add 300 parts of ion-exchanged water to the filter cake of [3], mix with a TK homomixer (10 minutes at 12,000 rpm), and then filter twice to obtain [filter cake 1]. It was.
[Filtration cake 1] was dried at 45 ° C. for 48 hours in a circulating drier, and sieved with a mesh of 75 μm to obtain [Toner 1].

[Example 2]
Next, [Toner 2] was obtained in the same manner as in Example 1 except that [Prepolymer 2] was used.

[Example 3]
Next, [Toner 3] was obtained in the same manner as in Example 1 except that [Prepolymer 3] was used.

[Example 4]
Next, [Toner 4] was obtained in the same manner as in Example 1 except that [Prepolymer 4] was used.

[Example 5]
Next, [Toner 5] was obtained in the same manner as in Example 1 except that [Monoester wax 2] (melting point 65 ° C., SP value 14.5, kinematic viscosity 8.4) was used.

[Example 6]
Next, [Toner 6] was obtained in the same manner as in Example 1 except that [Monoester wax 3] (melting point 68 ° C., SP value 19.7, kinematic viscosity 6.9) was used.

[Example 7]
Next, [Toner 7] was obtained in the same manner as in Example except that [Monoester wax 4] (melting point 55 ° C., SP value 15.5, kinematic viscosity 7.8) was used.

[Example 8]
Next, [Toner 8] was obtained in the same manner as in Example 1 except that [Monoester wax 5] (melting point 86 ° C., SP value 16.8, kinematic viscosity 9.4) was used.

[Example 9]
Next, [Toner 9] was obtained in the same manner as in Example 1 except that [Low Molecular Polyester 2] was used as Component B when preparing the emulsified slurry of Example 1.

[Example 10]
Next, [Toner 10] was obtained in the same manner as in Example 1 except that [Low Molecular Polyester 3] was used.

[Example 11]
Next, [Toner 11] was obtained in the same manner as in Example 1 except that [polyethylene wax 1] (melting point 75 ° C.), SP value 14.1 and kinematic viscosity 6.8) was used.

[Example 12]
Next, [Toner 12] was obtained in the same manner as in Example 1 except that [Carnauba wax 1] (melting point 83 ° C., SP value 15.4, kinematic viscosity 7.9) was used.

[Comparative Example 1]
Next, [Toner 13] was obtained in the same manner as in Example 1 except that [Prepolymer 5] was used.

[Comparative Example 2]
Next, [Toner 14] was obtained in the same manner as in Example 1 except that [Prepolymer 6] was used.

[Comparative Example 3]
Next, [Toner 15] was obtained in the same manner as in Example 1 except that [Monoester wax 6] (melting point 75 ° C., SP value 12.5, kinematic viscosity 8.2) was used.

[Comparative Example 4]
Next, [Toner 16] was obtained in the same manner as in Example 1 except that [Monoester wax 7] (melting point 67 ° C., SP value 22.4, kinematic viscosity 7.0) was used.

[Comparative Example 5]
Next, [Toner 17] was obtained in the same manner as in Example 1 except that [Prepolymer 7] was used.

[Comparative Example 6]
Next, [Toner 18] was obtained in the same manner as in Example 1 except that [Monoester wax 6] (melting point 97 ° C., SP value 15.4, kinematic viscosity 10.6) was used.

[Comparative Example 7]
Next, [Toner 19] was obtained in the same manner as in Example 1 except that [Monoester wax 7] (melting point 43 ° C., SP value 16.2 and kinematic viscosity 9.9) was used.

5% by mass of the prepared toners of Examples 1 to 12 and Comparative Examples 1 to 7 and 95% by mass of a ferrite carrier having a volume average particle size of 40 μm are mixed to prepare a two-component developer of toners 1 to 19. The fixing characteristics were evaluated as follows. The results are shown in Table 2.
The evaluation of the fixing property is 1.0 ± 0.1 mg / cm ^{2 using a} solid image on a plain paper and a thick paper transfer paper (type 6200 made by Ricoh and copy printing paper <135> made by NBS Ricoh) using Ricoh's imagio Neo450. The toner was developed so that the toner was developed, and the temperature of the fixing belt was adjusted to be variable, and the temperature at which no offset occurred on plain paper and the fixing lower limit temperature on thick paper were measured.
The lower limit fixing temperature was determined as the fixing lower limit temperature at the fixing roll temperature at which the residual ratio of the image density after rubbing the obtained fixed image with a pad was 70% or more.
Also, the temperature at which the offset occurs was measured.
About glossiness, the maximum value was made into maximum glossiness using POD gloss coat paper (128 / m < ² >) made from Oji Paper. The evaluation criteria are as follows.
<Fixing upper limit temperature>
Less than 160 ° C: ×
160-175 ° C .: △
175 or more: ○
<Fixing temperature limit>
130 ° C or higher: ×
120-130 ° C .: △
120 ° C. or less: ○
<Maximum glossiness>
Less than 25: ×
Less than 25-35:
35 or more: ○

(About FIGS. 1-6)
DESCRIPTION OF SYMBOLS 100 Electrophotographic copying machine 110 Photosensitive drum 120 Charger 130 Laser beam 140 Developing device 141 Developing roller 142 Developing roller 143 Paddle-shaped stirring member 144 Stirring member 145 Doctor 146 Toner replenishing part 147 Replenishing roller 150 Transfer device 160 Cleaning device 161 Cleaning Blade 162 Cleaning brush 170 Static elimination lamp 180 Paper feed device 191 Guide rail 192 Guide rail 510 Brush type charging device 511 Fur brush roller 512 Core metal 513 Brush portion 514 Power source 515 Photoconductor 600 Developer 601 Developer sleeve 602 Power source 603 Developer 604 Photosensitive Body 605 Toner 700 Fixing device 710 Heating roller 720 Fixing roller 721 Core metal 722 Elastic member 730 Fixing belt 731 Base 7 2 Heat generation layer 733 Intermediate layer 734 Release layer 740 Pressure roller 741 Core metal 742 Elastic member 760 Induction heating means 761 Excitation coil 762 Coil guide plate 763 Excitation coil core support member 770 Recording material 800 Process cartridge 801 Photoconductor 802 Charging Means 803 Development means 804 Developer 805 Phenomenon means 806 Cleaning means (FIG. 7)
DESCRIPTION OF SYMBOLS 100 Image forming apparatus 120Bk, 120C, 120M, 120Y Image writing part 130Bk, 130C, 130M, 130Y Image forming part 140 Paper feed part 150 Fixing device 160 Pair of registration rollers 170 Secondary transfer roller 180 Secondary transfer belt 200Bk, 200C, 200M, 200Y Developing device 210Bk, 210C, 210M, 210Y Photoconductor 215Bk, 215C, 215M, 215Y Charging device 220 Intermediate transfer belt 230Bk, 230C, 230M, 230Y Primary transfer device 241 Conductive roller 242 Conductive roller 243 Conductive roller 261 Conductive fur brush 262 Conductive fur brush 300Bk, 300C, 300M, 300Y Cleaning device (FIG. 8)
DESCRIPTION OF SYMBOLS 10 Intermediate transfer body 14 Support roller 15 Support roller 16 Support roller 17 Intermediate transfer body cleaning device 18 Image forming means 21 Exposure device 22 Secondary transfer device 23 Roller 24 Secondary transfer belt 25 Fixing device 26 Fixing belt 27 Pressure roller 28 Sheet Reversing device 32 Contact glass 33 First traveling body 34 Second traveling body 35 Imaging lens 36 Reading sensor 49 Registration roller 50 Paper feed roller 51 Manual tray 53 Manual paper feed path 55 Switching claw 56 Discharge roller 57 Paper discharge tray 58 Separation roller 62 Transfer Charger 100 Copier 110 Copier Main Body 120 Tandem Image Forming Device 130 Document Stand 142 Paper Feed Roller 143 Paper Bank 144 Paper Feed Cassette 145 Separation Roller 146 Paper Feed Path 147 Transport Roller 148 Paper Feed Path 200 Paper Feed Table 300 Scanner 400 Automatic document feeder (ADF)

JP 2002-108018 A JP 2002-214831 A JP 2003-167384 A JP 2006-276044 A JP 2000-039738 A JP 2007-148085 A JP 2004-246435 A

Claims (10)

At least a binder resin, a prepolymer composed of a modified polyester resin, an active hydrogen group compound that extends or crosslinks with the prepolymer, a colorant, and a solution or dispersion of an organic solvent in which a release agent is dissolved or dispersed, A toner production method for obtaining a toner by carrying out a crosslinking reaction and / or elongation reaction in an aqueous medium and removing the solvent from the obtained O / W type dispersion liquid,
The precursor for the prepolymer is an unmodified polyester copolymerized component an alcohol having a carbon ring, the precursor is Ri peak top molecular weight Mpt in the range near the 12000 ≦ Mpt ≦ 28000, and The ratio of the weight average molecular weight Mw to the number average molecular weight Mn, Mw / Mn is 4.5 or less,
The SP value SPr of the binder resin and the SP value SPw of the release agent are in a relationship of 3.0 <| SPr−SPw | <10.0,
And a melting point of the releasing agent is in the range of 50 ° C. to 90 ° C.   The toner production method according to claim 1, wherein the release agent is a monoester wax. The kinematic viscosity at 100 ° C. of the release agent is less than 10 mPa · s,
The toner production method according to claim 1.   The method for producing a toner according to claim 1, wherein the prepolymer has an isocyanate value of 0.4 to 0.7 mol%.   5. The method for producing a toner according to claim 1, wherein the prepolymer is contained in an amount of 5 to 13% by weight.   The toner manufacturing method according to claim 1, wherein the binder resin is a polyester resin.   The toner manufacturing method according to claim 1, wherein the binder resin contains at least amorphous polyester and crystalline polyester.   The toner production method according to claim 1, wherein a volume average particle diameter of toner particles of the toner is 3 to 7 μm.   9. The toner according to claim 1, wherein a ratio Dv / Dn of a volume average particle diameter Dv to a number average particle diameter Dn of toner particles of the toner is 1.0 to 1.25. Production method.   The toner manufacturing method according to claim 1, wherein the toner particles have an average circularity of 0.94 to 0.99.

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