JP2010249902A - Toner, image forming method, and image forming apparatus - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide: toner that reduce development gap scattering, reduce fog, reduce development gap scattering and fog even during toner supply, and reduce the dust generation amount; an image forming method; and an image forming apparatus. <P>SOLUTION: The toner includes: toner base particles containing at least a binder resin, a colorant, and a release agent; and alumina fine particles where the Raman intensity ratio (I<SB>al</SB>/I<SB>si</SB>) of the peak intensity (I<SB>si</SB>) at Raman shift of 400-600 cm<SP>-1</SP>of the silicon crystal (110) alignment surface of a silicon wafer obtained from a Raman scattering spectrum to the peak intensity (I<SB>al</SB>) at Raman shift of 1,400-1,600 cm<SP>-1</SP>of alumina fine particles is 0.01-0.5. In the image forming method and image forming apparatus, a developing device includes a developing roller having a spiral groove in the surface carrying the toner, supplies the toner, and performs development under an alternating electric field of alternating current frequency of 1-10 kHz. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

  The present invention relates to a toner, an image forming method, and an image forming apparatus.

  Conventionally, as an image forming apparatus, a photosensitive member such as a photosensitive drum or a photosensitive belt, which is a latent image carrier, is rotatably supported on the main body of the image forming apparatus, and an electrostatic latent image is formed on the photosensitive layer of the photosensitive member during an image forming operation. After forming the image, the latent image is visualized with toner by a contact method or a non-contact method, and then the visible image is directly transferred to a transfer material using a corona transfer or a transfer roller. There is a method in which a visible image is once transferred to an intermediate transfer medium such as a transfer drum or a transfer belt, and then retransferred to a transfer material. In these image forming apparatuses, two-component toner is generally known as the toner, and relatively stable development is possible. However, a change in the mixing ratio between the developer and the magnetic carrier is likely to occur. It is necessary to maintain it. One-component magnetic toner also has a problem that a clear color image cannot be obtained due to the opacity of the magnetic material.

The toner has a high fluidity and how to uniformly charge the toner in order to obtain a high quality recorded image by repeating the above-described steps. In particular, when applied to a non-contact AC developing system, it is necessary to improve the fluidity of the toner from the viewpoint of improving the flying property and weaken the adhesive force of the toner to the developing roller. From the viewpoint of improving the flight performance, it is necessary to release excessive triboelectric charges accumulated in the toner. In conventional toners, it is known that silica fine particles are externally added as a fluidity improver. However, since the silica fine particles have a high resistance of 10 ¹⁵ Ω · cm or more, a charge-up phenomenon occurs during charging, and image formation is performed. There is a problem that the image density is lowered by repeating the process.

  Therefore, alumina fine particles are externally added to the toner base particles, and the slight charge leakage action releases the excessive frictional charge accumulated in the toner to stabilize the toner triboelectric charge. In addition, attempts have been made to stabilize the charging performance of the photoreceptor by refreshing the surface of the photoreceptor by its polishing action.

  Nano-size alumina production methods include: (1) Low soda alumina fine particles: Showa Denko, Taiheiyo Random, (2) Dawsonite alumina fine particles: Daimei Chemical, Hinomoto, (3) Spark discharge method alumina: Iwatani Chemical (4) Flame hydrolysis method alumina: manufactured by Nippon Aerosil Co., Ltd. is known, and the alumina fine particles include α-alumina, γ-alumina, θ-alumina, and various forms such as a mixture thereof. It has been known. As alumina for external addition of toner, for example, α-alumina fine particles have a clear crystal structure, so that it is difficult to form oxygen defects (lattice defects) that are the starting points of the charge leakage action, and the function of stabilizing frictional charging is poor. Furthermore, since the α-alumina fine particles have a large particle diameter and high hardness, there is a defect that the polishing action tends to be manifested excessively. Polishing marks generated on the surface of the photoreceptor are the origin of image defects, or the photosensitive layer is excessive. There are problems such as shortening the service life by scraping.

  Further, γ-alumina fine particles, alumina fine particles coated with silicone oil, alumina fine particles subjected to surface treatment with a coupling agent, and the like have been proposed (Patent Documents 1 to 3). Γ-alumina, which is representative of transition alumina, easily forms oxygen defects (lattice defects) depending on its production method, and also contains a lot of structured water that is chemically adsorbed on the active Al-OH groups on the particle surface, so that it has a charge leakage effect. It is easy to express. However, there is a problem that the excessive leakage action makes it difficult to control the attenuation of triboelectric charge, and the environmental stability depending on the amount of moisture in the atmosphere is impaired. Furthermore, although γ-alumina can reduce the particle size, it has a feature that it easily forms secondary aggregates due to the effect of active Al—OH groups on the particle surface, and it was treated so as to adhere to the surface of the toner base particles. In some cases, the alumina free external additive present in a poorly dispersed state causes various problems as described below.

  In other words, the rising of triboelectric charging decreases with the printing of a large number of sheets, and a toner replenishment fogging phenomenon occurs particularly in a system for replenishing toner. When the developing operation of the toner in the developing device is repeated a number of times, the alumina fine particles of the external additive having a charge leakage effect from the surface are gradually lost due to being embedded or released in the toner base particles, and the rising of the triboelectric charge is reduced. To do. (1) When the developing device is a toner replenishing type that can replenish toner, toner used for development is newly replenished in addition to residual toner, or (2) the developing device can replenish toner In the case where the toner is not used, the regenerating and developing device is newly filled with toner in addition to the residual toner, and in any case, friction between the deteriorated toner damaged in the developing device and the new toner is caused. A difference in charging ability occurs during charging. In the one-component development method, when frictional charging between the developing roller, which is a toner carrier, and the toner causes a difference in frictional charging ability, the toner layer on the developing roller passes through the regulation passing mode when an image is formed after refilling with new toner or after refilling. In addition, there are problems such as scattering of the upper seal of the toner layer on the developing roller and fogging of the non-image forming portion on the photosensitive member. Also, in the two-component development method, when the frictional charge between the carrier and the toner has a difference in charging ability between the old and new toner, the developer layer on the magnet roller is scattered and the non-image forming portion on the photoconductor is fogged. Etc. occur.

  The mechanism of this development is that under the situation where deteriorated toner and new toner coexist in the developing device, the lower layer side of the toner layer formed on the toner particle carrying roller (developing roller) by the new toner having a good rise in frictional charging. The formation of the layer so that the old toner with inferior frictional charge rises as the surface layer side causes the old toner on the surface layer with inferior charge to be easily detached from the toner carrier during the developing operation.

  Further, the toner particles are carried on the surface of the developing roller and are charged while being rubbed by the surface having the pressure, the layer thickness regulating member, and the like by being pressed by the layer thickness regulating member. Some developing rollers are sandblasted on the toner carrying surface to provide fine irregularities on the surface, but the size, depth, shape, and arrangement of the depressions in the irregularities are not uniform. For this reason, for example, toner particles that have entered deep recesses are not rolled and may not be charged well. As described above, due to the unevenness of the uneven portions on the surface of the developing roller, there is a possibility that the toner particles are locally charged poorly, or the toner particles are trapped in small concave portions and filming may occur. Further, when the toner particles are not charged well, there is a possibility that the toner particles leak from the developing device and are scattered in the image forming apparatus or the image is fogged.

  In recent years, there is a concern that dust is contained in the cooling airflow discharged from the electrophotographic image forming apparatus to the outside of the apparatus, and that the dust may adversely affect the human body. There is a standard on dust particles in the atmosphere related to microparticulate matter (PM2.5) that is being considered by the Ministry of the Environment, and it is reported that legal guidelines will be disclosed as an environmental standard soon. It is expected that the external additive having charge leakage property is released from the toner surface and released outside the apparatus during the image forming operation, which contributes to the risk of dust generation. In recent years, the toner has been made smaller in size from the viewpoint of sharpening the image. In particular, it is considered that a small particle size toner having a volume average particle size of about 5 μm is mainly used. In a system that forms an image by applying an AC (alternating current) electric field between photoconductors, the toner moves onto the photoconductor while reciprocating in the developing electric field, so that the toner is activated in a cloud state in the developing electric field. There is also a concern that a part of the image may become dust by being multiplied by the airflow flowing in the image forming apparatus.

  As an alumina fine particle for external addition of toner, Patent Document 1 describes a hydrophobic γ-crystal alumina polishing substance, but does not describe the above-described problems caused by an alumina free external additive with respect to chargeability. Describes toner-added alumina fine particles obtained by the aluminum dowsonite method, and Patent Document 3 describes toner-added alumina fine particles obtained by forming amorphous alumina fine particles. However, there is no description on how to deal with the above-described problems in the alumina fine particles.

JP-A-3-191363 Japanese Patent Laid-Open No. 3-240068 Japanese Patent Laid-Open No. 8-184988

  In the present invention, even in a toner having a small particle size to which alumina fine particles are externally added, flying property, supply delay, regulation passing mole, upper seal scattering, fogging, toner replenishment regulation passing mole, toner supplement upper seal scattering, It is an object of the present invention to provide a toner, an image forming method, and an image forming apparatus in which development problems such as toner replenishment fog are solved and development gap scattering and toner replenishment development gap scattering are suppressed.

The toner of the present invention includes a toner base particle containing at least a binder resin, a colorant and a release agent, and a Raman shift of a silicon crystal [110] orientation plane of a silicon wafer obtained by a Raman scattering spectrum: 400 cm ^{−1 to} 600 cm ^{−. The} Raman intensity ratio (I _al / I _si ), which is the ratio of the peak intensity (I _si ) at 1 and the Raman shift of the alumina fine particles: peak intensity (I _al ) at 1400 cm ^{−1 to} 1600 cm ^−1, is 0.01 to 0.1. 5 containing alumina fine particles.

  The alumina fine particles are obtained by evaporating metallic aluminum with a DC arc plasma and oxidizing the vapor, or obtained by pyrolyzing ammonium dowsonite.

The toner base particles have a volume average particle diameter (D ₅₀ ) of 2.0 to 12.0 μm and are obtained by an emulsion aggregation method.

It said alumina particles, the BET specific surface area of 30m ² / g~250m ² / g, and wherein the number is an average particle diameter of 5 to 80 nm.

The image forming method of the present invention includes a photoconductor carrying an electrostatic latent image, and a developing device arranged to face the photoconductor in a non-contact state, and the developing device is carried on the photoconductor. A developing roller having a surface carrying toner for developing the electrostatic latent image and having helical grooves formed on the surface at an equal pitch in the axial direction and inclined in the axial direction and the circumferential direction. And a toner roller containing at least a binder resin, a colorant, and a release agent as the toner in the developing device, and a Raman scattering spectrum. Raman shift of the silicon crystal [110] orientation plane of the silicon wafer: 400 cm ^-1 peak at ～600Cm ^-1 intensity (I _si) and Raman shift of alumina particles: peak at 1400cm ^-1 ~1600cm ^-1 Intensity ratio Raman intensity ratio (I _al / I _si) is carried on said photosensitive member by supplying toner containing alumina particles is 0.01 to 0.5 electrostatic latent is a (I _al) The image is developed under an alternating electric field.

An image forming apparatus according to the present invention includes a photosensitive member carrying an electrostatic latent image, and an electrostatic latent image carried on the photosensitive member that is disposed so as to face the photosensitive member in a non-contact state. toner mother particles containing a colorant and a releasing agent, silicon crystal of the silicon wafer obtained by the Raman scattering spectrum [110] orientation plane Raman shifts: peak intensity at 400cm ^-1 ~600cm ^-1 (I _si) and alumina particles Raman shift of toner: A toner containing alumina fine particles having a Raman intensity ratio (I _al / I _si ) of 0.01 to 0.5, which is a ratio of peak intensity (I _al ) at 1400 cm ^{−1 to} 1600 cm ⁻¹ . A developing roller having a surface carrying toner for development and having helical grooves formed on the surface at an equal pitch in the axial direction and inclined with respect to the axial direction and the circumferential direction; And a developing device having a supply roller for supplying the toner, the electrostatic latent image carried on the photosensitive member being developed by the developing roller under an alternating electric field. .

  In the image forming method and the image forming apparatus described above, when the developing device is a toner replenishing type in which toner can be replenished, development is performed with newly replenished toner in addition to residual toner. In the case of a toner use-up type in which the toner cannot be replenished, development is performed with newly filled toner in addition to the residual toner.

FIG. 1 is a graph showing the Raman intensity ratio (I _al / I _si ) of alumina fine particles (Example 1) of the present invention. FIG. 2 is a graph showing the Raman intensity ratio (I _al / I _si ) in the alumina fine particles (Example 2) of the present invention. Figure 3 is a diagram showing a Raman intensity ratios (I _al / I _si) in the alumina particles of the present invention (Example 3). FIG. 4 is a diagram for explaining the outline of the image forming apparatus of the present invention. FIG. 5 is a diagram for explaining main components of the developing device. FIG. 6 is a view for explaining the surface shape of the developing roller. FIG. 7 is a view for explaining a cross section when the developing roller is cut along a plane passing through an axis. FIG. 8 is a diagram for explaining how the developing roller is formed by rolling. FIG. 9 is a diagram illustrating a procedure for forming the developing roller. FIG. 10 is a view for explaining a state in which the regulating blade is in contact with the developing roller carrying toner particles. FIG. 11 is a diagram showing a Raman intensity ratio (I _al / I _si ) in a comparative alumina fine particle (Comparative Example 1). FIG. 12 is a Raman spectrum diagram in the silicon crystal [110] orientation plane of the silicon wafer. FIG. 13 is a Raman spectrum diagram of the alumina fine particles (Example 1) of the present invention.

  Next, the toner base particles in the present invention are colored particles having a small particle diameter, and are preferably obtained by an emulsion aggregation method, but can be obtained by a phase inversion emulsification coalescence method or a pulverization method. But you can.

  In the emulsion aggregation method, polymerization is performed by dispersing monomers, polymerization initiators, emulsifiers (surfactants), etc. in water, and a dispersion consisting of the formed resin particles, a colorant, a release agent and necessary In accordance with the above, a charge control agent or the like and a dispersion liquid such as an aggregating agent (electrolyte) are mixed to obtain colored particles that are aggregated and heat-fused. The colored particles obtained in this way are preferably mixed with a dispersion of resin particles, and the colored particles are used as a core to attach and heat fuse the resin particles to form a coating (shell) to form a core-shell structure. The exposure of the mold component to the surface of the colored particles can be prevented to further prevent the wax (release agent) component from adhering to the developing roller or the like, and toner mother particles excellent in filming prevention can be obtained.

  Examples of the monomer in the emulsion aggregation method toner include styrene, o-methylstyrene, m-methylstyrene, p-methylstyrene, α-methylstyrene, p-methoxystyrene, p-ethylstyrene, vinyltoluene, and 2,4. -Dimethylstyrene, pn-butylstyrene, p-phenylstyrene, p-chlorostyrene, divinylbenzene, methyl acrylate, ethyl acrylate, propyl acrylate, n-butyl acrylate, isobutyl acrylate, acrylic acid n- Octyl, dodecyl acrylate, hydroxyethyl acrylate, 2-ethylhexyl acrylate, phenyl acrylate, stearyl acrylate, 2-chloroethyl acrylate, methyl methacrylate, ethyl methacrylate, propyl methacrylate, n-butyl methacrylate, meta Isobutyl toluate, n-octyl methacrylate, dodecyl methacrylate, hydroxyethyl methacrylate, 2-ethylhexyl methacrylate, stearyl methacrylate, phenyl methacrylate, acrylic acid, methacrylic acid, maleic acid, fumaric acid, cinnamic acid, ethylene Glycol, propylene glycol, maleic anhydride, phthalic anhydride, ethylene, propylene, butylene, isobutylene, vinyl chloride, vinylidene chloride, vinyl bromide, vinyl fluoride, vinyl acetate, vinyl propylene acid, acrylonitrile, methacrylonitrile, vinyl methyl ether , Vinyl ethyl ether, vinyl ketone, vinyl hexyl ketone, vinyl naphthalene and the like. Among these, a styrene allyl copolymer is preferable from the viewpoint of chargeability.

  Further, as colorants, carbon black, lamp black, magnetite, titanium black, chrome yellow, ultramarine blue, aniline blue, phthalocyanine blue, phthalocyanine green, Hansa Yellow G, rhodamine 6G, calco oil blue, quinacridone, benzidine yellow, rose bengal, Malachite Green Lake, Quinoline Yellow, C.I. I. Pigment red 48: 1, C.I. I. Pigment red 57: 1, C.I. I. Pigment red 122, C.I. I. Pigment red 184, C.I. I. Pigment yellow 12, C.I. I. Pigment yellow 17, C.I. I. Pigment yellow 97, C.I. I. Pigment yellow 180, C.I. I. Solvent Yellow 162, C.I. I. Pigment blue 5: 1, C.I. I. Dye and pigment such as CI Pigment Blue 15: 3 can be used alone or in combination.

  Examples of the mold release agent include paraffin wax, microwax, microcrystalline wax, cadilla wax, carnauba wax, rice wax, montan wax, polyethylene wax, polypropylene wax, oxidized polyethylene wax, oxidized polypropylene wax and the like. Among these, it is preferable to use polyethylene wax, polypropylene wax, carnauba wax, ester wax and the like.

  Examples of the polymerization initiator in the emulsion aggregation method include potassium persulfate, sodium persulfate, ammonium persulfate, hydrogen peroxide, 4,4′-azobiscyanovaleric acid, t-butyl hydroperoxide, benzoyl peroxide, 2,2 '-Azobis-isobutyronitrile and the like.

  Examples of the emulsifier (surfactant) include sodium dodecylbenzene sulfate, sodium tetradecyl sulfate, sodium pentadecyl sulfate, sodium octyl sulfate, sodium oleate, sodium laurate, potassium stearate, calcium oleate, dodecyl ammonium chloride, dodecyl ammonium bromide. , Dodecyl trimethyl ammonium bromide, dodecyl pyridinium chloride, hexadecyl trimethyl ammonium bromide, dodecyl polyoxyethylene ether, hexadecyl polyoxyethylene ether, lauryl polyoxyethylene ether, sorbitan monooleate polyoxyethylene ether, and the like.

  Examples of the flocculant (electrolyte) include sodium chloride, potassium chloride, lithium chloride, magnesium chloride, calcium chloride, sodium sulfate, potassium sulfate, lithium sulfate, magnesium sulfate, calcium sulfate, zinc sulfate, aluminum sulfate, and iron sulfate. Can be mentioned.

  The component ratio of the colored particles (toner base particles) is 3 to 10 parts by weight, preferably 4 to 8 parts by weight with respect to 100 parts by weight of the polymerization monomer, and 3 to 15 parts by weight for the colorant. Part by mass, preferably 5 to 10 parts by mass.

  Moreover, as a polymerization initiator in emulsion polymerization, it is 0.03-2 mass parts with respect to 100 mass parts of polymerization monomers, Preferably it is 0.1-1 mass part, As an emulsifier (surfactant), 0.01- As 0.1 mass part and a flocculant (electrolyte), it is 0.05-5 mass parts, Preferably it is used in the ratio of 0.1-2 mass parts.

  Moreover, it is good also as what is obtained by the phase inversion emulsification coalescence method. The phase inversion emulsification coalescence method is described in, for example, Japanese Patent No. 3,867,893. (1) An aqueous medium is obtained by emulsifying a mixture containing at least a polyester resin and an organic solvent in an aqueous medium. A first step of forming fine particles of the mixture therein, and then (2) a second step of adding a dispersion stabilizer and further adding electrolyte sequentially to combine the fine particles to produce an aggregate of fine particles, ( 3) After removing the organic solvent contained in the aggregate, fine particles are separated from the aqueous medium, washed, and then dried to sequentially perform a third step. In addition, when a styrene acrylic resin is used as the binder resin, it can be made into a binder resin having excellent charge stability due to its excellent moisture resistance, and when it is a polyester resin, it is excellent in transparency of the obtained image and suitable for a color image. I can do it.

The particle diameter of the colored particles (toner mother particles) in the present invention is 2.0 to 12.0 μm, preferably 50% volume average particle diameter (D ₅₀ ) as measured by Multisizer III type manufactured by Beckman Coulter. It is 0-9.0 micrometers. When the average particle diameter is 12.0 μm or less, even when a latent image is formed at a high resolution of 600 dpi or more, the resolution reproducibility can be excellent. When the thickness is 2.0 μm or less, the hiding property by the toner is lowered due to the reduction in the development efficiency, and the amount of the external additive used is increased to improve the fluidity, and as a result, the fixing performance tends to be lowered. There is.

As the toner base particle shape, toner particles having a shape close to a true sphere are preferable. Specifically, the toner base particles are represented by the following formula:
R = L ₀ / L ₁
{However, in the formula, L ₁ (μm) is the perimeter of the projected image of the toner particles to be measured, and L ₀ (μm) is a perfect circle having an area equal to the area of the projected image of the toner particles to be measured (completely The perimeter of a geometric circle). }
The average circularity (R) represented by the formula is 0.95 to 0.99, preferably 0.96 to 0.98. The average circularity of the toner is a value measured with a flow type particle image analyzer (FPIA2100 manufactured by Sysmex). As a result, the transfer efficiency is high, and even when continuous printing is performed, there is little fluctuation in the transfer efficiency, the charge amount is stabilized, and the toner has excellent cleaning properties.

  A method for producing toner base particles will be described. Hereinafter, “part” means part by mass.

(Preparation of resin fine particle dispersion)
・ Styrene ... 370g
・ N-Butyl acrylate ... 30g
・ Acrylic acid ・ ・ ・ 8g
・ Dodecanethiol ・ ・ ・ 24g
-Carbon tetrabromide ... 4g.

  6 g of nonionic surfactant (Nonipol 400: manufactured by Sanyo Kasei Co., Ltd.) and 10 g of anionic surfactant (Neogen SC: manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) were ion-exchanged. The mixture was emulsified and dispersed in a flask dissolved in 550 g of water, and 50 g of ion-exchanged water having 4 g of ammonium persulfate dissolved therein was added thereto while slowly mixing for 10 minutes. After carrying out nitrogen substitution, the inside of the flask was stirred and heated in an oil bath until the contents reached 70 ° C., and emulsion polymerization was continued for 5 hours. As a result, a resin fine particle dispersion in which resin particles having an average particle diameter of 150 nm, Tg = 58 ° C., and weight average molecular weight Mw = 11500 was obtained. The solid content concentration of this dispersion was 40% by mass.

(Preparation of colorant dispersion)
-Cyan pigment B15: 3 ... 60 g
・ Nonionic surfactant (Nonipol 400: Sanyo Kasei Co., Ltd.) ・ ・ 5g
-Ion exchange water ... 240g.

  The above components are mixed and dissolved, stirred for 10 minutes using a homogenizer (Ultra Turrax T50: manufactured by IKA), and then dispersed by an optimizer to disperse colorant particles having an average particle size of 250 nm. A colorant dispersion was prepared.

(Preparation of release agent dispersion)
・ Polyethylene wax (PW725: Toyo Petrolite Co., Ltd.) ・ 100g
・ Ionic surfactant (Neogen RK: Daiichi Kogyo Seiyaku Co., Ltd.) ・ ・ 5g
-Ion exchange water ... 200g.

  The solution in which the above components are mixed is heated to 95 ° C. and sufficiently dispersed with a homogenizer (Ultra Turrax T50: manufactured by IKA), and then dispersed with a pressure discharge homogenizer, and the average particle size is 210 nm. A release agent dispersion liquid in which release agent particles are dispersed was prepared.

(Preparation of toner base particles)
・ Resin fine particle dispersion prepared above 234 parts ・ Colorant dispersion prepared above 30 parts ・ Release agent dispersion prepared above 40 parts ・ Polyaluminum chloride (Asada Chemical) "PAC100W") .. 1.8 parts. Ion exchange water. 600 parts.

The above components were mixed and dispersed in a round stainless steel flask using a homogenizer (Ultra Turrax T50: manufactured by IKA), and then heated to 50 ° C. while stirring the inside of the flask in a heating oil bath. After maintaining at 50 ° C. for 30 minutes, it was confirmed that aggregated particles having a D ₅₀ (volume average particle diameter) of 4.5 μm were formed. Further, the temperature of the heating oil bath was raised and maintained at 56 ° C. for 1 hour, and D ₅₀ (volume average particle diameter) was 5.3 μm.

Thereafter, 26 parts of the resin fine particle dispersion was added to the dispersion containing the aggregate particles, and then the temperature of the heating oil bath was raised to 50 ° C. and held for 30 minutes. After adding 1N sodium hydroxide to the dispersion containing the aggregated particles and adjusting the pH of the system to 5.0, the stainless steel flask was sealed and heated to 95 ° C. while continuing to stir for 4 hours. Retained and encapsulated. After cooling, it was filtered off, washed four times with ion exchange water, and then lyophilized to obtain toner base particles. The toner base particles had a D ₅₀ (volume average particle diameter) of 5.5 μm.

Next, the alumina fine particles that characterize the present invention will be described.
In the Raman scattering spectrum of alumina fine particles, Raman shift occurs due to, for example, the crystal structure and lattice defects, and α-alumina particles having a 100% α-phase, “Tymicron TM-DAR, primary particle size 0. In the case of “16 μm” or “RA-40, primary particle size 1.4 μm” manufactured by Iwatani Chemical Co., Ltd., the Raman shift shows a sharp peak Raman intensity at 1400 cm ^{−1 to} 1600 cm ⁻¹ . Even in transition alumina fine particles, for example, “C805, particle size 13 nm, γ phase 2/3, δ phase 1/3” manufactured by Nippon Aerosil Co., Ltd. the shift 1400cm ^-1 ~1600cm ^-1, as shown in FIG. 11, showing a rather strong Raman intensity.

In contrast, Raman scattering spectrum in the transition alumina particles shown in Examples 1 to 3 is different from the above-mentioned α- alumina particles, etc., it found that Raman intensity is weak in the Raman shift 1400cm ^-1 ~1600cm ^-1 did. In the alumina particles having a peak between Raman shift 1400cm ^-1 ~1600cm ^-1, the magnitude of the Raman intensity, the clear how having any relation with the leakage of the charge of the alumina fine particles can not be inferred, Transition alumina fine particles have more lattice defects such as oxygen defects than α-alumina particles, have excellent potential leakage (conductivity), and can be less scattered toner and dust. It was found that there was a lot of toner scattered without being captured by the electric field, resulting in a lot of dust.

Although the Raman spectrum generally shows the same tendency with respect to the measurement value of the same sample, the Raman signal intensity at the obtained CCD count varies considerably depending on the measurement device configuration, its setting conditions, sample form, etc. To do. Therefore, in the present invention, when specifying the peak intensity (I _al ) of the Raman intensity of the alumina fine particles, the Raman intensity (I _si ) of the Si wafer having extremely stable quality is simultaneously measured, and the obtained intensity ratio ( _Ial / _Isi ) was used to compare the Raman intensities of different alumina particles. FIG. 13 shows a Raman spectrum diagram of the alumina fine particles shown in Example 1, and FIG. 12 shows a Raman spectrum diagram of the Si crystal [110] orientation plane of the Si wafer measured simultaneously. FIG. 1 shows the relationship between the Raman intensity ratio (I _al / I _si ) and the Raman shift (cm ⁻¹ ) obtained based on FIGS. 12 and 13 for the alumina fine particles of the present invention shown in Example 1. The Raman intensity ratio (I _al / I _si ) and the Raman shift (cm ⁻¹ ) from which a Raman spectrum of the Si crystal [110] orientation plane of the Si wafer measured simultaneously with the Raman spectrum of the alumina fine particles shown in Example 2 was obtained. FIG. 2 shows the relationship. The same applies to FIG. As apparent from the comparison of FIGS. 1 to 3 with the alumina fine particles of the comparative example shown in FIG. 11, the alumina fine particles of the present invention shown in FIGS. 1 to 3 have a Raman intensity ratio (I _al / I _si ) of 0. In the range of 01 to 0.5, it can be seen that, unlike the alumina fine particles of the comparative example shown in FIG. 11, a toner having excellent potential leakage (conductivity) can be obtained.

The Raman spectrometer used in the present invention and the measurement conditions are as follows.
"JRS SYSTEM 2000" manufactured by Renishaw
Excitation laser: 630 nm
Laser power: 3mW
Laser sbot diameter: 1 μm ¹⁾ (Set so that the laser focus is minimized.
Measurement integration time: 30 sec
Objective lens: × 50
Si wafer: Si crystal [100] orientation, mirror finish (surface roughness 1 nm or less) ²⁾
The Si electric field polarization direction and the Si crystal [110] orientation plane coincide with each other.
Set the angle of the wafer ³⁾
Alumina fine particle sample shape: φ11mm × 1mm tablet shape (press pressure 2ton) ⁴⁾
Add 5% by mass of Yamato glue (mainly tapioca starch) as a binder.
24 hours after room molding
¹⁾ : Since the spectral intensity changes with the focus of the laser, from the viewpoint of measurement reproducibility, it is preferable to set the laser focus to be the smallest and to the extent that the laser diameter fluctuates by about 20%.

^2): not stable spectra obtained by sandblasting the wafer.

³⁾ : The Si wafer has a [100] orientation that is generally used, but the angle of the Si wafer is set so that the laser electric field polarization direction coincides with the [110] orientation plane of the Si crystal. If this setting is not made, the spectral intensity will be weakened to about 2/3.

⁴⁾ : If the alumina fine particles are in a powder form, the unevenness is severe and a stable spectral intensity cannot be obtained. Therefore, as described above, a specific tablet shape is used for measurement.
Further, it is added that there is an error of about 10% as the measurement accuracy of the spectrum intensity.

The alumina fine particles in Example 1 are “Tymicron TM-100, Al ₂ O ₃ , θ-alumina phase as a main phase, known as transition alumina particles, and have a primary particle size of 14 nm, a BET specific surface area of 132 m ² / In addition, the alumina fine particles in Example 2 have “Tymicron TM-300, Al ₂ O ₃ , γ-alumina phase as a main phase, manufactured by Daimei Chemical Co., Ltd., a primary particle size of 7 nm, and a BET specific surface area of 225 m ^2. a / g ', also alumina fine particles in example 3, CI Kasei Co., Ltd. _{"Nano · Tek, Al 2 O 3} , γ- alumina phase as a main phase, a crystalline containing a small amount of α- alumina phase Spherical fine particles with a primary particle size of 30 nm and a BET specific surface area of 49.3 m ² / g ”. Transition alumina fine particles are prepared by various production methods. For example, alumina fine particles having a Raman intensity ratio (I _al / I _si ) of 0.01 to 0.5 are obtained by pyrolyzing ammonium dowsonite. What is obtained is also obtained by evaporating metallic aluminum with a direct current arc plasma and oxidizing the vapor.

  The BET specific surface area in the external additive particles is determined using “Fully Automatic Specific Surface Area Meter Macsorb HM model-1201” manufactured by Mountec Co., Ltd.

  The “particle diameter” is observed with a transmission electron microscope, and 100 particle diameters in a visual field are measured to obtain an average particle diameter.

  The alumina fine particles in the present invention exhibit an effect of charge leakage under an AC electric field and stabilize the frictional charge of the toner, and also refresh the surface of the photoconductor by the polishing action of the alumina fine particles to charge the photoconductor. It is thought that it stabilizes. Furthermore, when the developing device can replenish toner, in a toner replenishing type developing device that is newly replenished toner in addition to residual toner, or when the developing device cannot replenish toner, In a toner-use type developing device that is newly filled toner in addition to residual toner, toner replenishment fogging is reduced and residual memory generated due to free external additives remaining on the photoreceptor is reduced. be able to.

  The alumina fine particles of the present invention are externally added at a ratio of 0.2 parts by mass to 5.0 parts by mass, preferably 0.5 parts by mass to 2.0 parts by mass with respect to 100 parts by mass of the toner base particles. Good. If the amount of treatment with respect to the toner base particles is larger than this, there is a problem that the charge leakage action is excessively generated or free external additives are generated, and if it is less, the desired polishing effect cannot be obtained.

  In the examples described later, the alumina fine particles which have not been hydrophobized are used, but may be hydrophobized with a silane organic compound such as alkylalkoxysilane, siloxane, silane, or silicone oil. It is particularly preferable to use alkylalkoxysilane, such as vinyltrimethoxysilane, vinyltriethoxysilane, γ-methacryloxypropyltrimethoxysilane, vinyltriacetoxysilane, methyltrimethoxysilane, methyltriethoxysilane, isobutyltrimethoxysilane, Examples include dimethyldimethoxysilane, dimethyldiethoxysilane, trimethylmethoxysilane, hydroxypropyltrimethoxysilane, phenyltrimethoxysilane, n-hexadecyltrimethoxysilane, and n-octadecyltrimethoxysilane.

  In addition to alumina fine particles, (1) hydrophobic small silica particles (hereinafter referred to as hydrophobic small silica particles), (2) hydrophobic monodispersed spherical large silica particles, and (3) positively charged silica as external toner additives Try particles.

(1) The hydrophobic small silica particles have a number average primary particle diameter of 7 to 16 nm, preferably 10 to 12 nm, a bulk specific gravity of 0.1 to 0.2 g / cm ³ and a two-component charge amount (5 min). Value) of −20 to −80 μC / g, “R8200” manufactured by Nippon Aerosil Co., Ltd., and “RX200 (bulk specific gravity of 0.02 to 0.06 g / cm ³ , two-component charge amount ( 5 min value) −100 to −300 μC / g) ”. Both are obtained by vapor phase oxidation (dry method) of silicon halogen compounds, and differ in bulk specific gravity and two-component charge amount (5 min value).

  The smaller the number average primary particle diameter of the hydrophobic small silica particles, the higher the fluidity of the obtained toner. However, when the number average primary particle diameter is smaller than 7 nm, the silica fine particles are embedded in the toner base particles when externally added. Conversely, if the number average primary particle diameter exceeds 16 nm, the fluidity may be deteriorated. The hydrophobic small silica particles are added in an amount of 0.5 to 3.0 parts by weight, preferably 1.0 to 2.0 parts by weight, based on 100 parts by weight of the toner base particles. Due to the charging property and high fluidity, the formation of the compressed agglomerates in the rubber thin layer regulating portion can be suppressed.

  The bulk specific gravity is obtained by pouring the powder through a funnel into a 100 ml measuring cylinder, stopping the injection when it reaches 100 ml, measuring the weight at this time, and substituting it into the following equation.

Bulk specific gravity (g / cm ³ ) = {(weight after sample injection) − (weight before sample injection)} / {volume of graduated cylinder (100 ml)}.

  Next, (2) the hydrophobic monodispersed spherical large silica particles have a number average primary particle size of 50 to 250 nm, preferably 80 to 150 nm. Hydrophobic monodisperse spherical large silica particles are spherical with a Wadell sphericity of 0.6 or more, preferably 0.8 or more. Monodispersed spherical silica fine particles are obtained by a sol-gel method that is a wet method, and have a specific gravity of 1.3 to 2.1. When the hydrophobic monodisperse spherical large silica particles have an average particle size of less than 50 nm, it becomes impossible to maintain the fluidity and charging stability by preventing the embedding of the fine particles of silica particles on the surface of the toner base particles. In addition, the spacer effect cannot be obtained, and if it is larger than 250 nm, it is difficult to adhere to the toner base particles and to be easily detached from the surface of the toner base particles.

Examples of the hydrophobic monodisperse spherical large silica particles include “Seahoster KE-P10S2” (number average primary particle diameter 100 nm) manufactured by Nippon Shokubai Co., Ltd. The number average primary particle diameter is 100 nm, hydrophobized (surface) treatment with silicone oil, the true specific gravity is 2.2, the bulk specific gravity is 0.25 to 0.35, the BET specific surface area is 10 to 14 m ² / g, two components Charge amount (5 min value) is 0 to −50 μC / g.

  The hydrophobic monodispersed spherical large silica particles are added in an amount of 0.2 to 2.0 parts by weight, preferably 0.5 to 1.5 parts by weight, based on 100 parts by weight of the toner base particles. When the amount of hydrophobic monodispersed spherical large silica particles is less than 0.2 parts by mass, the toner filling density increases, and the toner layer is reduced when the toner layer is regulated with a regulating blade when the developing roller rotates. It becomes difficult, and there are problems of regulation leakage and scattering. Further, if added more than 2.0 parts by mass, the toner layer filling density is too low, and when the toner layer passes through the regulating blade during rotation of the developing roller, a part of the toner leaks without being held by the developing roller, Further, due to the layer thickness formation unevenness that occurs in the developing roller cycle of the toner layer, when a full-color image is output, the density uniformity in the paper feeding direction is impaired, and the developing roller cycle unevenness appears.

  The addition ratio (mass ratio) of the large particle size silica (2) to the small particle size silica (1) may be 1: 4 to 4: 1, preferably 2: 3 to 3: 2. It is preferable for imparting fluidity to the film and obtaining long-term charging stability. The large particle size silica and the small particle size silica are in a total amount of 1.25 to 5.0 parts by mass, preferably 2.0 to 3.0 parts by mass with respect to 100 parts by mass of the toner base particles in consideration of the mixing ratio of both. Part by mass is added.

  The silica fine particles are preferably hydrophobized. By making the surface of the negatively chargeable silica fine particles hydrophobic, the fluidity and chargeability of the toner are further improved. Hydrophobization of silica fine particles is performed by using a silane compound such as hexamethyldisilazane or dimethyldichlorosilane; or a silicone oil such as dimethylsilicone, methylphenylsilicone, fluorine-modified silicone oil, alkyl-modified silicone oil, or epoxy-modified silicone oil. For example, a method commonly used by those skilled in the art, such as a wet method or a dry method.

(3) The positively chargeable silica particles have a number average primary particle diameter of 20 nm to 40 nm. The positively chargeable silica fine particles are preferably hydrophobized, and are added to reduce the change in chargeability with respect to changes in the external environment, maintain stable chargeability, and improve toner fluidity. The Hydrophobization of the positively chargeable silica fine particles is performed using an aminosilane coupling agent, amino-modified silicone oil, or the like. Hydrophobic positively chargeable silica fine particles are commercially available NA50H manufactured by Nippon Aerosil Co., Ltd. (crystal is amorphous, spherical, number average primary particle size is 30 nm, hydrophobized (surface) treated with hexamethyldisilazane and aminosilane. , The true specific gravity is 2.2, the bulk specific gravity is 0.0671, the BET specific surface area is 44.17 m ² / g, the carbon content is 2% or less, the two-component charge amount (5 min value) 40 μC / g), or manufactured by Cabot Corporation. TG820F and the like are exemplified.

  As a method for adding the above-mentioned external additives to the toner base particles, a Henschel mixer (made by Mitsui Miike Co., Ltd.), a Q-type mixer (made by Mitsui Mining Co., Ltd.), a mechano-fusion system (made by Hosokawa Micron Co., Ltd.), a mechano mill (Okada Seiko Co., Ltd.) Etc.). When multistage processing is performed using a Henschel mixer, the processing operation conditions at each stage are appropriately selected from the range of a rotational peripheral speed of 30 to 50 m / s and a processing time of 2 to 15 minutes.

  In addition, the order of addition of the external additives is preferably a multi-stage process consisting of three stages. The toner base particles are first treated with alumina fine particles as the first stage, and then with hydrophobic monodispersed spherical large silica particles as the second stage. Small silica particles are treated and adhered, and positively charged silica fine particles are preferably treated as the third stage. As a result, the charge distribution can be adjusted at the time of regulating the thin layer, and a negatively chargeable one-component non-magnetic toner that can suppress the formation of an electrostatic aggregate due to a charge-up phenomenon can be obtained.

In addition, in the present invention, other hydrophobized external additives, for example, hydrophobic medium silica particles {fumed silica, “RX50” manufactured by Nippon Aerosil Co., Ltd., within a range that does not impair the purpose of adding the external additive particles described above. “True specific gravity 2.2, volume average particle diameter D ₅₀ = 40 nm (standard deviation = 20 nm)}, a metal salt selected from zinc, magnesium, calcium and aluminum of higher fatty acids which are metal soap particles, magnesium stearate, Calcium stearate, zinc stearate, monoaluminum stearate, trialuminum stearate, etc. may be added externally, and zinc oxide, strontium oxide, tin oxide, zirconia oxide, magnesium oxide, indium oxide, titanium oxide, oxidation Fine particles of metal oxide such as cerium, fine particles of nitride such as silicon nitride, carbon Fine particles of carbides such as silicon nitride, resin particles, fine particles of metal salts such as calcium sulfate, barium sulfate, calcium carbonate, strontium titanate, and inorganic fine particles such as a composite thereof may be added.

The toner of the present invention has a flow softening temperature (Tf1 / 2) of 90 ° C. to 140 ° C. and a glass transition temperature (Tg) in the range of 40 ° C. to 70 ° C. The flow softening temperature (Tf1 / 2) was measured using a flow tester (CFT-500) manufactured by Shimadzu Corporation with a nozzle diameter of 1.0 mmΦ × 1.0 mm, a load of 10 kg per unit area (cm ² ), and 6 ° C. per minute. It is a value measured at the rate of temperature rise. Further, the glass transition temperature (Tg) is a value measured at a rate of temperature increase of 10 ° C. per minute by a second run method using a “differential scanning calorimeter (DSC-220C)” manufactured by Seiko Instruments Inc.

Next, the image forming method and the image forming apparatus of the present invention will be described.
FIG. 4 is a diagram for explaining the outline of the image forming apparatus of the present invention. In FIG. 4, the printer 10 includes a charging unit 30, an exposure unit 40, and a developer holding unit 50 along the rotation direction of the photosensitive member 20. A primary transfer unit 60, an intermediate transfer member 70, a cleaning unit 75, and a secondary transfer unit 80, a fixing unit 90, and the like.

  The photoreceptor 20 has a cylindrical conductive substrate and a photosensitive layer formed on the outer peripheral surface thereof, is rotatable around a central axis, and rotates clockwise as indicated by an arrow. The charging unit 30 is a device for charging the photoconductor 20, and the exposure unit 40 is a device for forming a latent image on the photoconductor 20 charged by irradiating a laser. The exposure unit 40 irradiates the charged photoconductor 20 with a modulated laser beam based on the image signal. Then, the laser beam is turned on / off at a predetermined timing, and a dot-like latent image is formed in a grid-divided area on the photoreceptor 20 that rotates at a predetermined speed.

  The developing device holding unit 50 converts the latent image formed on the photoreceptor 20 into black (K) toner contained in the black developing device 51, magenta (M) toner contained in the magenta developing device 52, and cyan developing device. This is an apparatus for developing using cyan (C) toner accommodated in 53 and yellow (Y) toner accommodated in the yellow developing device 54. The developing device holding unit 50 can move the positions of the four developing devices 51, 52, 53, and 54 by rotating. Each time the photosensitive member 20 rotates once, one of the four developing devices 51, 52, 53, 54 is selectively opposed to the photosensitive member 20, and the opposed developing devices 51, 52, 53, 54, The latent images formed on the photoconductor 20 are sequentially developed with the toner accommodated in 54.

  The primary transfer unit 60 is a device for transferring a single color toner image formed on the photoconductor 20 to the intermediate transfer body 70. When four color toners are sequentially transferred in a superimposed manner, the full color toner is transferred to the intermediate transfer body 70. An image is formed. The intermediate transfer member 70 is an endless belt, and is driven to rotate at substantially the same peripheral speed as the photosensitive member 20. The secondary transfer unit 80 is a device for transferring a single color toner image or a full color toner image formed on the intermediate transfer body 70 to a recording medium such as paper, film, or cloth.

  The fixing unit 90 is a device for fusing a single color toner image or a full color toner image transferred onto a recording medium onto a recording medium such as paper to form a permanent image. The cleaning unit 75 is provided between the primary transfer unit 60 and the charging unit 30 and has a rubber cleaning blade 76 that is in contact with the surface of the photoconductor 20. The cleaning unit 75 is disposed on the intermediate transfer body 70 by the primary transfer unit 60. After the toner image is transferred, the toner T remaining on the photoconductor 20 is scraped off and removed by the cleaning blade 76.

  The developing device holding unit 50 includes a black developing device 51 containing black (K) toner, a magenta developing device 52 containing magenta (M) toner, a cyan developing device 53 containing cyan (C) toner, and yellow. (Y) A yellow developing unit 54 containing toner is provided. Since the developing units have the same configuration, the cyan developing unit 53 will be described below.

  FIG. 5 is a diagram for explaining the developing device as a representative of the cyan developing device, and is a cross-sectional view showing the main components of the developing device. The developing device 53 includes a housing 540 that contains toner T, a developing roller 510 as an example of a toner particle carrying roller for carrying toner, a toner supply roller 550 for supplying toner to the developing roller 510, and a developing roller 510. A regulating blade 560 as an example of a layer thickness regulating member for regulating the layer thickness of the carried toner, an upper seal 520 for sealing an upper gap between the housing 540 and the developing roller 510, a housing 540 and the developing roller An end seal 527 for sealing a gap on the end side with 510 is provided.

  The housing 540 is manufactured by welding an integrally molded resin upper housing portion 542 and lower housing portion 544, and a toner storage portion serving as a storage portion for storing the toner T therein. 530 is formed. The toner storage portion 530 has two toner storage portions, that is, a first toner storage portion 530a and a second toner, by a partition wall 545 for partitioning the toner T that protrudes inward from the inner wall (in the vertical direction in FIG. 5). It is divided into the accommodating portion 530b.

  The upper portions of the first toner storage portion 530a and the second toner storage portion 530b communicate with each other. In the state shown in FIG. 4, the movement of the toner T is restricted by the partition wall 545. However, when the developing device holding unit 50 rotates, the toner stored in the first toner storage portion 530a and the second toner storage portion 530b is temporarily moved to the upper communicating side of the developing position. When the toner is collected and returned to the state shown in FIG. 5, the toners are mixed and returned to the first toner container 530a and the second toner container 530b. That is, the toner T in the developing device is agitated by the rotation of the developing device holding unit 50. For this reason, in this embodiment, the stirring member is not provided in the toner storage portion 530, but a stirring member for stirring the toner T stored in the toner storage portion 530 may be provided. As shown in FIG. 5, the housing 540 has an opening 572 in the lower portion, and a developing roller 510 described later is provided so as to face the opening 572.

  The toner supply roller 550 includes an elastic roller portion 550a formed of, for example, urethane foam, and a shaft body 550b that serves as a rotation center of the roller portion 550a. The toner supply roller 550 is supported by the housing 540 at both ends of the shaft body 550b, so that the toner supply roller 550 is rotatably supported around the shaft body 550b. The roller portion 550a is accommodated in the first toner accommodating portion 530a (inside the housing 540) of the housing 540, and supplies the toner T accommodated in the first toner accommodating portion 530a to the developing roller 510. The toner supply roller 550 is provided vertically below the first toner storage portion 530a. The toner T accommodated in the first toner accommodating portion 530a is supplied to the developing roller 510 by the toner supply roller 550 below the first toner accommodating portion 530a. Further, the toner supply roller 550 peels off the excess toner T remaining on the developing roller 510 after development from the developing roller 510.

  The toner supply roller 550 and the developing roller 510 are assembled to the housing 540 while being pressed against each other. Therefore, the roller portion 550a of the toner supply roller 550 is in contact with the developing roller 510 in an elastically deformed state. The toner supply roller 550 rotates in a direction (clockwise in FIG. 4) opposite to the rotation direction of the developing roller 510 (counterclockwise in FIG. 5). The shaft body 550b is below the rotation center axis of the developing roller 510.

  The developing roller 510 carries the toner T and conveys it to a developing position facing the photoconductor 20. The developing roller 510 is made of metal and is made of an aluminum alloy such as 5056 aluminum alloy or 6063 aluminum alloy, or an iron alloy such as STKM, and is subjected to nickel plating, chrome plating, or the like as necessary. May be. On the surface of the developing roller 510, a spiral groove is provided at the center in the axial direction of the developing roller 510. The surface shape of the developing roller 510 will be described in detail later.

  Further, the developing roller 510 is supported at both ends in the longitudinal direction, and is rotatable about the central axis. As shown in FIG. 5, the developing roller 510 rotates in a direction (counterclockwise in FIG. 5) opposite to the rotation direction of the photoconductor 20 (clockwise in FIG. 5). The central axis is below the central axis of the photoconductor 20.

  Further, as shown in FIG. 5, there is a gap between the developing roller 510 and the photosensitive member 20 in a state where the yellow developing device 54 faces the photosensitive member 20. That is, the yellow developing device 54 develops the latent image formed on the photoconductor 20 in a non-contact state. When developing the latent image formed on the photoconductor 20, an alternating electric field is formed between the developing roller 510 and the photoconductor 20.

  The regulating blade 560 applies a charge to the toner T carried on the developing roller 510 and regulates the layer thickness of the toner T carried on the developing roller 510. The regulation blade 560 has a rubber part 560a and a rubber support part 560b. The rubber part 560a is made of silicon rubber, urethane rubber or the like, and the rubber support part 560b is a thin plate having spring properties such as phosphor bronze or stainless steel. The rubber part 560a is supported on the short side of the rubber support part 560b along the longitudinal direction of the rubber support part 560b, and the other end side of the rubber support part 560b is supported by the blade support metal plate 562. In this state, it is attached to the housing 540 via the blade support sheet metal 562. Further, a blade back member 570 made of malt plane or the like is provided on the side opposite to the developing roller 510 side of the regulating blade 560.

  Here, the rubber portion 560 a is pressed from the central portion of the developing roller 510 to both ends by the elastic force due to the bending of the rubber support portion 560 b. Further, the blade back member 570 prevents the toner T from entering between the rubber support portion 560b and the housing 540, stabilizes the elastic force due to the bending of the rubber support portion 560b, and provides rubber from the back of the rubber portion 560a. The rubber portion 560 a is pressed against the developing roller 510 by urging the portion 560 a toward the developing roller 510. Therefore, the blade back member 570 improves the uniform contact property of the rubber portion 560a to the developing roller 510.

  The end of the regulating blade 560 opposite to the side supported by the blade support metal plate 562, that is, the tip is not in contact with the developing roller 510, and a portion away from the tip by a predetermined distance is the developing roller. 510 is in contact with a width. In other words, the regulating blade 560 is not in contact with the developing roller 510 at the edge, but is in contact with the antinode on the flat surface of the rubber portion 560a. The regulating blade 560 is disposed so that the tip thereof faces the upstream side in the rotation direction of the developing roller 510, and is in a so-called counter contact. The contact position where the regulating blade 560 contacts the developing roller 510 is below the central axis of the developing roller 510 and below the central axis of the toner supply roller 550.

  The rubber support portion 560b is longer than the rubber portion 560a in the axial direction of the developing roller 510, and extends outward from both ends of the rubber portion 560a. An end seal 527 made of, for example, a nonwoven fabric having a thickness thicker than that of the rubber portion 560a is attached to the same surface as the rubber portion and 560a at the extended portion of the rubber support portion 560b. At this time, the end surface of the rubber portion 560 a in the axial direction is in contact with the side surface of the end seal 527.

  The end seal 527 is provided so as to come into contact with both end portions of the surface of the developing roller 510 where no groove portion is provided when the developing roller 510 is attached, and has a width extending from the end portion of the developing roller 510 to the outside. is doing. Further, the end seal 527 extends sufficiently longer than the tip of the rubber portion 560 a of the regulating blade 560. When the regulating blade 560 is attached to the housing 540, the end seal 527 is placed along a portion of the housing 540 formed so as to face the outer peripheral surface of the developing roller 510, and closes the gap between the housing 540 and the developing roller 510. .

  The upper seal 520 prevents the toner T in the yellow developing device 54 from leaking out of the device, and collects the toner T on the developing roller 510 that has passed through the developing position into the developing device without being scraped off. The upper seal 520 is a seal made of a polyethylene film or the like. The upper seal 520 is supported by a seal support sheet metal 522 and is attached to the housing 540 via the seal support sheet metal 522. A seal urging member 524 made of malt plain or the like is provided on the opposite side of the upper seal 520 from the developing roller 510 side. The upper seal 520 is developed by the elastic force of the seal urging member 524. 510 is pressed. The contact position at which the upper seal 520 contacts the developing roller 510 is above the central axis of the developing roller 510.

(Operation of cyan developing device 53)
In the cyan developing device 53 configured in this manner, and supplies the toner T to the toner supplying roller 550 is accommodated in the toner accommodating portion 530 to the developing roller 510. The toner T supplied to the developing roller 510 reaches the contact position of the regulating blade 560 as the developing roller 510 rotates, and when passing through the contact position, an electric charge is applied and the layer thickness is regulated. Is done.

  The charged toner T on the developing roller 510 reaches a developing position facing the photoconductor 20 by further rotation of the developing roller 510, and a latent image formed on the photoconductor 20 under an alternating electric field at the developing position. For development. The toner T on the developing roller 510 that has passed the developing position by further rotation of the developing roller 510 passes through the upper seal 520 and is collected in the developing device without being scraped off by the upper seal 520. Further, the toner T still remaining on the developing roller 510 can be peeled off by the toner supply roller 550.

(Development roller surface shape)
FIG. 6 is a conceptual diagram for explaining the surface shape of the developing roller. FIG. 7 is a cross-sectional view for explaining a cross section when the developing roller is cut along a plane passing through an axis. In FIG. 6, the groove on the surface of the developing roller 510 is shown as a straight line for convenience, but since the groove is formed in a spiral shape, it is formed so that it looks exactly like a curve.

  The developing roller 510 is provided with a concavo-convex portion for supporting toner particles in the central portion 510a in the axial direction, and both end portions 510b have smooth peripheral surfaces so that the end seals 527 are in close contact with each other.

  As shown in FIG. 6, in the central portion 510 a of the developing roller 510 in this embodiment, a spiral groove 511 that is inclined with respect to the axial direction and the circumferential direction of the developing roller 510 and is formed at an equal pitch in the axial direction. Is formed. The groove portion 511 is formed in two types with different inclination angles with respect to the axial direction and the circumferential direction of the developing roller 510. The two types of groove portions 511 intersect with each other to form a lattice shape, and the top surface 512a of the convex portion 512 surrounded by the two types of groove portions 511 is formed in a substantially square shape. Further, the two types of the groove portions 511 are formed so that one of the two diagonal lines of the square of the top surface 512a of the convex portion 512 is along the circumferential direction.

  That is, one of the two types of grooves 511 is formed in a spiral shape so as to form an angle of 45 ° clockwise with the axis of the developing roller 510, and the other is counterclockwise with the axis of the developing roller 510. It is formed in a spiral shape so as to form an angle of 45 ° in the direction. For this reason, the angle at which one groove 511a and the other groove 511b intersect is 90 °. In addition, since the pitch in the axial direction of the developing roller 510 of the one groove portion 511a and the other groove portion 511b is equal, the shape of the top surface 512a of the convex portion 512 surrounded by the two types of groove portions is substantially square. It becomes.

  As shown in FIG. 7, the two types of groove portions 511 are each formed at an interval of 80 μm in the axial direction of the developing roller 510, and an inclined portion 511 d extending from the top surface 512 a of the convex portion 512 to the bottom surface 511 c of the groove portion 511. Is formed such that the intersecting angle α of the virtual plane obtained by extending the two inclined surfaces forming the groove 511 in the direction of the axis C is 90 °.

  Further, the depth of the groove portion 511, that is, the distance from the top surface 512a of the convex portion 512 to the bottom surface 511c of the groove portion 511 is formed to be constant at about 10 μm. Here, the depth of the groove 511 is preferably set to 1.5 times or more and 3.0 times or less of the average volume particle diameter of the toner. When the volume average particle diameter of the toner is 5.5 μm, It is good to set so that it may be 8 micrometers or more and 17 micrometers or less.

  Such a developing roller 510 is formed by rolling. FIG. 8 is a diagram for explaining how the developing roller 510 is formed by rolling. FIG. 9 is a diagram illustrating a procedure for forming the developing roller.

  The developing roller 510 is formed from a cylindrical hollow material. The cylindrical material is first cut to a length that can form a central portion 510a for carrying toner as the developing roller 510 and an end portion 510b with which the end seal 527 abuts, and the cylindrical member 515 is cut out. (S001). In the cylindrical member 515, a step portion 510c (FIG. 6) for fitting the flange 513 having the shaft of the developing roller 510 is formed in the inner peripheral portion of both end portions by cutting (S002). Here, the flange 513 includes a disk-shaped flange main body 513a having a diameter that is press-fitted into the formed stepped portion 510c, and a shaft portion 513b that protrudes perpendicularly to the disk surface from the center thereof. ing.

  Next, the flange 513 having the shaft portion 513b is fitted into the cylindrical member 515 having the step portion 510c formed inside the both end portions so that the shaft portion 513b protrudes outward of the cylindrical member (S003). .

  Thereafter, the cylindrical member 515 in which the flange 513 is fitted is supported by the shaft portions 513b at both ends and rotated around the shaft, and the outer peripheral surface of the cylindrical member 515 is slightly cut over the entire circumference, thereby The surface of the cylindrical member 515 is polished so that the entire region is concentric with the shaft, that is, a certain distance L from the shaft, thereby forming the non-rolled developing roller 509 (S004).

  The cylindrical member 515 whose surface has been polished is rolled by an apparatus having a die 900 as two types of processing tools as shown in FIG. 8 to form two types of grooves 511a and 511b on the surface (S005). ). The rolling device arranges the workpiece (here, the non-rolled processing developing roller 509) while the two types of dies 900 arranged at opposite positions are rotating in the same direction, and the two types of dies 900 are arranged. The unrolled developing roller 509 is pressed, and the unrolled developing roller 509 is conveyed in the axial direction while rotating in the direction opposite to the die 900. The die 900 is provided with blades 900a for forming the above-described grooves 511a and 511b. The blades 900a are formed on the surface of the non-roll processed developing roller 509 with the blades. An inclination is provided so that the grooves 511a and 511b are orthogonal. Here, the part where the die 900 is brought into contact with the surface of the non-rolling processing developing roller 509 is a blade 900a. However, in rolling, the work is not actively cut, and the work is crushed by pressing force. Acts to form a depression. Further, during this rolling, the non-rolled developing roller 509 is not contacted with the die 900 at both ends 510b, leaving a smooth surface without unevenness at both ends 510b. deep. That is, the distance L from the axis C is constant between the top surface 512a of the convex portion 512 where the die 900 is not in contact with the central portion 510a of the developing roller 510 and the both end portions 510b not to be processed by rolling. Since it has been cut as is, it is located at an equal distance from the axis C. The surface 510d of the developing roller 510 is substantially covered with the bottom surfaces 511c of the grooves 511a and 511b that are recessed by contacting the die 900 and the non-processed surface that the die 900 does not contact. The developing roller 510 formed by rolling may be subjected to, for example, electroless Ni—P plating, electroplating, or hard chrome plating, if necessary.

  To such a developing roller 510, toner is supplied from the toner supply roller 550 between the end seals 527 abutted at both ends 510b, and the thickness of the toner layer is regulated at the pressing position of the regulation blade 560. Is done. At this time, the regulating blade 560 is pressed across the both end portions 510b and the central portion 510a of the developing roller 510, but the both end portions 510b of the developing roller 510 and the top surface 512a of the convex portion 512 are at a distance L from the axis C. Therefore, the regulating blade 560 presses the developing roller 510 in a substantially flat state without being largely bent. For this reason, for example, an extremely large gap does not occur between the surface 510d of the developing roller 510 and the regulating blade 560 even in the vicinity of the boundary between the both end portions 510b and the central portion 510a.

  Further, since the depth of the groove portion 511 is 1.5 times or more and 3.0 times or less of the volume average particle diameter of the toner particles, the toner particles that have entered the groove portion 511 are in the depth direction at any position in the groove portion 511. No more than three. That is, a large amount of toner particles do not enter the groove portion 511, and most of the toner particles come into contact with either the surface 510 d of the developing roller 510 or the surface of the regulating blade 560 when pressed by the regulating blade 560. Therefore, each toner particle T is easy to roll, and the toner particles do not easily stay in the groove 511, so that the toner particles T can be charged well. For this reason, the toner particles are reliably carried on the developing roller 510 and used for development, and in combination with the fact that no extremely large gap is generated between the surface 510d of the developing roller 510 and the regulating blade 560, It is possible to prevent the toner particles T from leaking outside the developing devices 51, 52, 53, 54.

  FIG. 10 is a view for explaining a state in which the regulating blade is in contact with the developing roller carrying toner particles. In particular, the groove 511 of the developing roller 510 of the present embodiment has a depth of 10 μm, and is set to 1.5 times or more and 3.0 times or less as compared with the volume average particle diameter (5.5 μm) of the toner particles T. ing. For this reason, since the regulating blade 560 is made of rubber and follows the unevenness of the surface 510d of the developing roller 510, each toner particle T is reliably charged in the entire area including the convex portion 512 and the groove portion 511 of the central portion 510d. It is possible to make it. It is possible to reliably carry the toner on the developing roller 510 to improve transferability during development and to prevent toner from leaking outside the developing device.

  That is, if unevenness having a non-uniform size, depth, shape, or the like is formed on the surface 510d of the developing roller 510, the toner particles that enter the deep recesses of the carried toner particles are difficult to roll and are not easily charged. . In addition, when grooves along the circumferential direction are formed at predetermined intervals in the axial direction, the position in the axial direction of the photoconductor 20 facing the groove does not change even when the photoconductor 20 rotates. In the developed toner image, there is a tendency that only the portion facing the groove portion has a high density. On the other hand, when the groove portion is formed along the axial direction, the rotation direction of the toner particle carrying roller and the direction of the groove portion are almost orthogonal to each other, so that the carried toner particles are difficult to roll and are not easily charged.

  According to the developing devices 51, 52, 53, and 54 and the developing roller 510 of the present embodiment, the surface 510d of the developing roller 510 is inclined with respect to the axial direction and the circumferential direction and has a spiral groove portion at an equal pitch in the axial direction. Since 511 is formed, the toner particles T are moved while being rotated as the developing roller 510 rotates, so that the toner particles T can be charged satisfactorily. Further, as the developing roller 510 rotates, the position where the photoconductor 20 and the groove 511 face each other changes sequentially in the axial direction and the circumferential direction, so that it is possible to suppress the occurrence of density unevenness in the developed toner image. Is possible.

  Further, since the developing roller 510 of the present embodiment has two types of groove portions 511a and 511b having different inclination angles, the toner particles T are moved in two types of directions along the groove portions 511a and 511b. It will be. For this reason, it is possible to prevent the toner particles T from moving and being biased in only one predetermined direction. Further, since the two types of the groove portions 511a and 511b intersect each other to form a lattice shape, the toner particles T that have started to roll along the one groove portion 511a (511b) are transferred from the middle to the other. It is possible to roll along the groove part 511b (511a). For this reason, it is possible to more effectively suppress the deviation of the moving direction of the toner particles T.

  Furthermore, since the top surface 512a of the convex portion 512 surrounded by the two types of groove portions 511 is a square, and one diagonal line of the square is along the circumferential direction, the convex portion 512 is positioned along the circumferential direction. The two apex angles and the two apex angles positioned along the axial direction are both right angles, and the two types of grooves 511a and 511b have the same angle of inclination with respect to the circumferential direction and the axial direction. . For this reason, the toner particles T can be easily moved in the circumferential direction and the axial direction as well. For this reason, it is possible to uniformly charge the toner particles by rolling them more uniformly.

  Further, the toner particle T carried on the surface of the developing roller 510 has its layer thickness restricted by the plane of the rubber part 560 a of the restriction blade 560, so that the toner particle T is carried on the surface of the developing roller 510, particularly the convex part 512. The toner particles T are not completely scraped off by the regulating blade 560. That is, it is possible to regulate the layer thickness of the toner particles T in a state where the toner particles T are carried on the groove portions 511 and the convex portions 512 of the developing roller 510. Further, since the toner particles T carried on the surface 510d are pressed by the flat surface of the regulating blade 560, any one of the surface of the developing roller 510, the regulating blade 560, and the toner particles and the toner particles T are mutually connected. It is possible to charge well by rubbing.

  In addition, when the toner can be replenished, the developing device uses a mixed toner with the newly replenished toner in addition to the residual toner, or when the toner cannot be replenished, the residual toner In addition to this, a mixed toner with newly filled toner is used.

  Hereinafter, the present invention will be described in more detail with reference to examples.

Example 1
(Toner preparation)
After 2 kg of the toner base particles obtained by the above-mentioned emulsion aggregation method were charged into a Henschel mixer (20 L), alumina fine particles (“Tymicron TM-” manufactured by Daimei Chemical Co., Ltd.) were added at an added amount per 100 g of toner base particles (hereinafter the same). 100, Al ₂ O ₃ , θ-alumina phase as the main phase, primary particle size 14 nm, BET specific surface area 132 m ^{2 /} g ”) 1.5 g was added and treated at a peripheral speed of 40 m / s for 2 minutes.

  Next, 1.5 g of hydrophobic monodispersed spherical large silica particles (“KEP10S2” manufactured by Nippon Shokubai Co., Ltd., primary particle size 100 nm, silicone oil-treated product), and hydrophobic small silica particles (“RX200” manufactured by Nippon Aerosil Co., Ltd.) primary particle size A 12 nm, HMDS (hexamethylsilazane) treated product) 2.0 g was added and treated at a peripheral speed of 40 m / s for 2 minutes.

  After the treatment, coarse particles were removed with a sonic sieve using a metal mesh having a mesh size of 63 μm to obtain the toner of the present invention.

(Example 2)
In the preparation of the toner of Example 1, alumina fine particles manufactured by Daimei Chemical Co., Ltd. “Tymicron TM-300, Al ₂ O ₃ , γ-alumina phase as the main phase, primary particle size 7 nm, BET specific surface area 225 m ² / g” The toner of Example 2 was obtained in the same manner as in Example 1 except that the amount was changed to 0.5 g.

(Example 3)
The toner of Example 1 was prepared except that the alumina fine particles were replaced with 1.5 g of “Nano Tek, Al ₂ O ₃ , primary particle size 30 nm, BET specific surface area 49.3 m ^{2 /} g” manufactured by Cai Kasei Co., Ltd. The toner of Example 3 was obtained in the same manner as Example 1.

(Comparative Example 1)
In the preparation of the toner of Example 1, alumina fine particles “AEROXIDE C805, crystal system (ratio): γ phase 2/3, δ phase 1/3, primary particle size 13 nm, BET specific surface area 100 m ² / g” manufactured by Nippon Aerosil Co., Ltd. The toner of Comparative Example 1 was obtained in the same manner as in Example 1 except that 0.8 g was used.

(Image formation)
Each obtained toner was mounted on the image forming apparatus (LP9000C, manufactured by Seiko Epson Corporation) shown in FIG.

  The developing roller is a roll-formed product, and the surface of an iron hollow shell having a diameter of φ = 18 mm and a length of 370 mm is formed in the shape shown in FIGS. 6 and 7, that is, with an angle of 45 ° in the axial and circumferential directions and a pitch of 80 μm. The groove has a top width of 30 μm, a non-top width of 50 μm, and a depth of 10 μm.

  The layer thickness regulating member is made of silicon rubber, urethane rubber or the like having a thickness of 2 mm and a rubber hardness of JIS-A of 65 degrees, and is supported by the layer thickness regulating member support member. The layer thickness regulating member support member is composed of a thin plate and a thin plate supporting member, and supports the layer thickness regulating member at the short side-end portion. The thin plate is made of phosphor bronze, stainless steel or the like having a thickness of 0.15 mm and has a spring property. The thin plate directly supports the layer thickness regulating member, and presses the layer thickness regulating member against the developing roller by its urging force. As a regulation form of the layer thickness regulating member, a regulation form (so-called edge regulation) is adopted in which the leading end in the short direction and the thickness direction of the layer thickness regulating member is located in the contact nip having a predetermined width. The supply roller was made of urethane sponge having an outer diameter of φ19 and Asker F hardness of 70 °, and was pressed against the developing roller at a contact depth of 1.0 mm.

The process speed (photoconductor peripheral speed) is 210 mm / s, the photoconductor dark potential is −550 V, the photoconductor light potential is −50 V, the developing roller peripheral speed is 336 mm / s, and the supply roller peripheral speed is 504 mm / s. The photosensitive member-developing roller peripheral speed ratio is 1.6, the developing roller-supply roller peripheral speed ratio is 1.5,
Photoconductor-developing roller gap 100 μm
Photoconductor-developing roller AC bias component Vpp: 1100 V
Photoconductor-developing roller DC bias component Vdc: -300 V
Photoconductor-developing roller AC frequency (f): 6 kHz
Photoconductor-developing roller AC Duty (stripping side application time ratio): 60%
Under these conditions, a color image was formed by the AC jumping development method. Note that the toner amount adjustment patch sensor was not operated. Moreover, the test environment was 22-24 degreeC / 45-55% RH.

  Next, evaluation items and evaluation methods in actual machines for the toners of Examples 3 to 3 and Comparative Examples 1 and 2 will be described, and the evaluation results are shown in Table 1.

(1) Flight characteristics (OD value)
This indicates the level of development capability when forming a full-color (solid) image, and is expressed by the size of the image density and its uniformity. An average OD value and a minimum OD value of a total of nine points combining the three positions of the front / center / rear of the image and the left / center / right of the image are used.
Lv4 (◯): State where average OD value is 1.30 or more and minimum OD value is 1.20 or more Lv3 (Δ): State LV2 where average OD value is 1.20 or more and minimum OD value is 1.10 or more ( X): State where average OD value is 1.10 or more and less than 1.20 Lv1 (x): state where average OD value is less than 1.10.

(2) Supply delay The uniformity of the image density in the paper feed direction (exposure sub-scanning direction) decreases from the second round of the developing roller to the rear edge with respect to the first round of the developing roller cycle, which is the leading edge of the solid (solid) image. A phenomenon in which a decrease in density (scratch) occurs and was judged visually.
Lv4 (◯): A state in which there is no density decrease in the region from the first rotation of the developing roller cycle, which is the leading edge of the image, to the trailing edge of the image (not distinguishable even through watermarking)
Lv3 (◯): a state in which there is no decrease in density in the region from the first rotation of the developing roller cycle, which is the leading edge of the image, to the trailing edge of the image (can be determined by seeing through)
Lv2 (Δ): A state in which density reduction due to supply delay occurs in a part after the second rotation of the developing roller cycle Lv1 (Δ): Density reduction due to supply delay exceeds half of the development roller cycle in the second and subsequent cycles The state that occurred.

(3) Regulation passing molet This is a phenomenon in which when the toner layer on the developing roller passes through the regulating blade, a part of the toner leaks without being held by the developing roller, and was visually evaluated in the following four stages. 3 or more is acceptable according to the following criteria.
Lv4 (◯): No toner leakage from the regulating blade onto the developing roller, and no contamination with toner.
Lv3 (Δ): A state in which toner leakage occurs intermittently when the developing roller rotates, and a toner amount smaller than the size of sesame particles is adhered to such an extent that the ground can be seen.
Lv2 (x): A state in which toner leakage occurs intermittently when the developing roller rotates, and the toner amount adheres and accumulates to such an extent that the background cannot be seen.
Lv1 (x): Toner leakage occurs intermittently when the developing roller rotates, and toner continues to leak without restriction.

(4) Upper seal scattering When the toner layer on the developing roller passes through the upper seal, it means that a part of the toner is scattered without being held by the developing roller. The judgment criteria are as follows.
Lv4 (◯): toner scattering on the developing roller does not occur at the upper seal collecting portion and the toner is not soiled Lv3 (Δ): the scattered toner is thin enough to see the ground on a part of the holder / housing Adhered state Lv2 (x): Scattered toner is accumulated until part of the base on the holder / housing is no longer visible Lv1 (x): Scattered toner appears on the holder / housing over half the area of the base Accumulated until it disappears.

(5) Scattering of developing gap When the toner on the developing roller is transferred to the photosensitive member due to the alternating electric field applied between the photosensitive member and the developing roller, a part of the toner activated by the reciprocating motion in the alternating electric field is Phenomenon that is not trapped by the developing electric field but is scattered by the surrounding air current. The quantification of the scattering is based on the adhesion state of the toner trapped on the 1 cm square adhesive tape surface located at the point moved 10 mm in the vertical direction of the line connecting the central axes from the closest point between the photoconductor and the developing roller. The following score is determined against the limit sample of the microscope magnified image to be created.
Lv4 (◯): The state where the toner trapped on the adhesive surface is 5 pieces / cm ² or less Lv3 (Δ): The toner trapped on the adhesive surface is more than 5 pieces / cm ² , 20 states / cm ² or less lv2 (×): more than adhesive trapped toner 20 on surface / 1 cm ^2, 100/1 cm ² or less states Lv1 (×): a state in which the toner captured on the adhesive surface exceeds 100/1 cm ² .

(6) Fog (OD value)
The amount of fog on the photoconductor (OPC) is determined by forcibly stopping the image formation process halfway when printing a white solid pattern, and the white solid (background) fog toner remaining on the photoconductor is removed from the mending tape (Sumitomo). Transfer and collect with 3M). After the transfer and recovery of the tape is affixed to J paper (Fuji Xerox Co., Ltd.), the OD value (optical reflection density) is measured with a Macbeth densitometer. The OD value of the tape alone was about 0.1, and the difference of the OD value was taken as the fog toner density.
Lv4 (◯): State in which the OD value for fog toner is 0.10 or less Lv3 (Δ): State in which the OD value for fog toner is 0.15 or less, and exceeds 0.10 Lv2 (×): fog toner The OD value for the minute is 0.20 or less and is more than 0.15 Lv1 (×): The OD value for the fog toner is more than 0.20.

(7) More than a toner supply regulation passage After forming a white solid image corresponding to 6000 sheets of A4 size and consuming the fog toner amount, new toner is supplied to the developing device by an amount corresponding to 10 of the remaining toner weight. Immediately after the new toner is replenished to the developing device, the regulation passage leakage of the toner layer on the developing roller is temporarily increased. The determination of the toner replenishment regulation passage mole is a method for determining the normal fog regulation passage mole. Follow the same procedure.
Lv4 (◯): No toner leakage from the regulating blade onto the developing roller, and no contamination with toner.
Lv3 (Δ): A state in which toner leakage occurs intermittently when the developing roller rotates, and a toner amount smaller than the size of sesame particles is adhered to such an extent that the ground can be seen.
Lv2 (x): A state in which toner leakage occurs intermittently when the developing roller rotates, and the toner amount adheres and accumulates to such an extent that the background cannot be seen.
Lv1 (×): A state in which toner leakage occurs continuously when the developing roller rotates, and toner continues to leak without restriction.

(8) Toner replenishment on the sticker scattering A solid white image corresponding to 6000 sheets of A4 size is formed, and after the amount of fog toner is consumed, new toner is replenished to the developing device by an amount corresponding to 10 of the remaining toner weight. To see the phenomenon that the upper seal scattering on the toner roller on the developing roller temporarily increases immediately after the new toner is replenished to the developing device. Follow the same procedure.
Lv4 (◯): toner scattering on the developing roller does not occur at the upper seal collecting portion and the toner is not soiled Lv3 (Δ): the scattered toner is thin enough to see the ground on a part of the holder / housing Adhered state Lv2 (x): Scattered toner is accumulated until part of the base on the holder / housing is no longer visible Lv1 (x): Scattered toner appears on the holder / housing over half the area of the base Accumulated until it disappears.

(9) Toner replenishment / development gap scattering After forming a solid white image corresponding to 6000 sheets of A4 size and consuming the fog toner amount, new toner is replenished to the developing device by an amount corresponding to 10% of the remaining toner weight. A phenomenon in which the development gap scattering that occurs in a white solid image formed immediately after new toner is supplied to the developing device temporarily increases. The determination of toner replenishment / development gap scattering is carried out in the same procedure as the normal fog determination method.
Lv4 (◯): The state where the toner trapped on the adhesive surface is 5 pieces / cm ² or less Lv3 (Δ): The toner trapped on the adhesive surface is more than 5 pieces / cm ² , 20 states / cm ² or less lv2 (×): more than adhesive trapped toner 20 on surface / 1 cm ^2, 100/1 cm ² or less states Lv1 (×): a state in which the toner captured on the adhesive surface exceeds 100/1 cm ² .

(10) Toner replenishment fog A white solid image corresponding to 6000 sheets of A4 size is formed, and after the amount of fog toner is consumed, new toner is replenished to the developing device by an amount corresponding to 10% of the remaining toner weight. This is a phenomenon in which the fog generated in the solid white image formed immediately after the new toner is supplied to the developing device is temporarily increased. The determination of the toner supply fog amount is performed in the same procedure as the normal fog determination method. .
Lv4 (◯): State in which the OD value for fog toner is 0.10 or less Lv3 (Δ): State in which the OD value for fog toner is 0.15 or less, and exceeds 0.10 Lv2 (×): fog toner The OD value for the minute is 0.20 or less and is more than 0.15 Lv1 (×): The OD value for the fog toner is more than 0.20.

  As can be seen from Table 1, the toner of the present invention has less development gap scattering and less fogging, and also less toner development gap scattering and less fogging even when toner is replenished.

  INDUSTRIAL APPLICABILITY The present invention can reduce development gap scattering and fog, and can provide toner with little development gap scattering and little fog even when toner is replenished. Can provide.

10 printers, 20 photoconductors, 30 charging units, 40 exposure units, 50 developing device holding units, 60 primary transfer units, 70 intermediate transfer units, 75 cleaning units, 80 secondary transfer units, 90 fixing units, 509 non-rolling processing Development roller, 510 development roller, 510a center, 510b end (both ends), 510c step, 510d surface, 511 groove,
511a One groove portion, 511b The other groove portion, 511c bottom surface, 511d inclined portion, 512 convex portion, 512a top surface, 513 flange, 513a flange body, 513b shaft portion, 515 cylindrical member, 520 upper seal, 522 seal support sheet metal, 524 Seal urging member, 527 end seal, 530 toner accommodating portion, 530a first toner accommodating portion, 530b second toner accommodating portion, 540 housing, 542 upper housing portion, 544 lower housing portion, 545 partition wall, 550 toner supply roller 550a roller part, 550b shaft body, 560 regulating blade, 560a rubber part, 560b rubber support part, 562 blade support sheet metal, 570 blade back member, 572 opening, T is toner

Claims (8)

At least a binder resin, and toner base particles containing a colorant and a releasing agent, silicon crystal of the silicon wafer obtained by the Raman scattering spectrum [110] orientation plane Raman shifts: peak intensity at 400cm ^-1 ~600cm ^-1 (I _si ) and Raman shift of alumina fine particles: alumina fine particles having a Raman intensity ratio (I _al / I _si ) of 0.01 to 0.5, which is a ratio of peak intensity (I _al ) at 1400 cm ^{−1 to} 1600 cm ⁻¹ . A toner characterized by containing. The toner according to claim 1, wherein the alumina fine particles are obtained by evaporating metallic aluminum with a direct current arc plasma and oxidizing the vapor, or obtained by pyrolyzing ammonium dowsonite. The toner according to claim 1, wherein the toner base particles have a volume average particle diameter (D ₅₀ ) of 2.0 to 12.0 μm and are obtained by an emulsion aggregation method. Alumina particles, the toner of claim 1, wherein the BET specific surface area 30m ² / g~250m ² / g, and a number average particle size 5 to 80 nm. A photosensitive member carrying an electrostatic latent image; and a developing device arranged to face the photosensitive member in a non-contact state, and the developing device develops the electrostatic latent image carried on the photosensitive member. And a developing roller having a spiral groove formed on the surface at an equal pitch in the axial direction and an inclined surface with respect to the axial direction and the circumferential direction. A toner roller including at least a binder resin, a colorant, and a release agent as the toner, and a silicon crystal of a silicon wafer obtained by a Raman scattering spectrum [110] Raman shift of the orientation surface: 400 cm ^-1 peak at ～600Cm ^-1 intensity (I _si) and Raman shift of fine alumina particles: Oh a ratio of peak intensity at 1400cm ^-1 ~1600cm ^-1 (I _al) A toner containing alumina fine particles having a Raman intensity ratio (I _al / I _si ) of 0.01 to 0.5 is supplied to develop the electrostatic latent image carried on the photoreceptor under an alternating electric field. An image forming method. When the developing device is a toner replenishing type that allows toner to be replenished, development is performed with newly replenished toner in addition to residual toner, and the developing device is a toner use-up type that does not allow toner to be replenished. 6. The image forming method according to claim 5, wherein the development is performed with a newly filled toner in addition to the residual toner. The photosensitive member carrying the electrostatic latent image is disposed opposite to the photosensitive member in a non-contact state, and the electrostatic latent image carried on the photosensitive member includes at least a binder resin, a colorant, and a release agent. toner mother particles and, a silicon wafer obtained by the Raman scattering spectrum silicon crystal [110] orientation plane Raman shifts: 400 cm peak intensity at ^{-1 ~600cm -1} (I _si) and Raman shift of alumina particles: 1400 cm ^-1 ~ A toner for development is carried by a toner containing alumina fine particles having a Raman intensity ratio (I _al / I _si ) of 0.01 to 0.5, which is a ratio of peak intensity (I _al ) at 1600 cm ⁻¹ . A developing roller having a surface and a helical groove formed at an equal pitch in the axial direction and inclined to the axial direction and circumferential direction on the surface; It is location, and a developing device having a supply roller for supplying the toner, an image forming apparatus, characterized in that developed by the developing roller under AC electric field to the electrostatic latent image carried on the photoreceptor. When the developing device is of a toner replenishing type that allows toner to be replenished, the developing device uses a newly replenished toner in addition to the residual toner, and the developing device is a toner exhausting type that does not allow the toner to be replenished. 8. The image forming apparatus according to claim 7, wherein the developing is performed with a newly filled toner in addition to the residual toner.

Images