JP6358500B2 - Cleaning blade, image forming apparatus, and process cartridge - Google Patents

Description

  The present invention relates to a cleaning blade, an image forming apparatus, and a process cartridge.

2. Description of the Related Art Conventionally, in an electrophotographic image forming apparatus, unnecessary transfer residual toner adhering to a surface after transferring a toner image to a transfer paper or an intermediate transfer body is removed as a cleaning unit. Has been removed by.
As a cleaning member of this cleaning device, one that uses a strip-shaped cleaning blade is well known because it can generally be simplified in configuration and has excellent cleaning performance. The cleaning blade is made of an elastic member such as polyurethane rubber. Then, the base end of the cleaning blade is supported by a support member, the tip ridge line portion is pressed against the surface of the image carrier, and the toner remaining on the image carrier is damped and scraped off and removed.

  However, as shown in FIG. 7A, the polyurethane cleaning blade 62 is pressed against the surface of the image carrier 123 to increase the frictional force between the image carrier 123 and the cleaning blade 62, and the cleaning blade 62. Is pulled in the moving direction of the image carrier 123, the leading edge portion 62 c of the cleaning blade 62 is rolled. Further, if the cleaning is continued with the leading edge portion 62c of the cleaning blade 62 being curled, as shown in FIG. 7B, the cleaning blade 62 is separated from the leading edge portion 62c of the blade leading surface 62a by several [μm]. Local wear will occur at the spot. If the cleaning is further continued in such a state, the local wear increases, and the leading edge portion 62c is eventually lost as shown in FIG. 7C. If the leading edge portion 62c is missing, the toner cannot be properly cleaned, resulting in poor cleaning.

  Attempts have been made to increase the hardness of the tip ridge line portion so that the tip ridge line portion is not easily deformed in order to prevent the tip ridge line portion from coming into contact with the surface of the image carrier of the cleaning blade. For example, Patent Document 1 describes a cleaning blade in which a surface layer made of an ultraviolet curable resin harder than an elastic member is provided so as to cover the tip ridge line portion of the cleaning blade, and the tip ridge line portion has a high hardness. Patent Document 2 describes a cleaning blade in which an elastic member is impregnated with an ultraviolet curable material and then subjected to an ultraviolet irradiation treatment to form a hardened layer on a tip ridge. Further, Patent Document 3 discloses that a hardened layer formed by impregnating an ultraviolet curable material into a tip ridge line portion of an elastic member, and a surface layer made of an ultraviolet curable resin covering the tip ridge line portion of the elastic member on which the hardened layer is formed. A cleaning blade is described.

  However, since the cleaning blade proposed in Patent Documents 1 to 3 has a high crosslinking density of the ultraviolet curable resin used, the surface layer provided on the contact portion has a large curing shrinkage when cured, and the surface layer There is a problem that a crack occurs in the tip or the tip ridge line portion is worn by friction over time, and the surface layer is peeled off to cause a chip in the tip ridge line portion of the elastic member.

  The present invention has been made in view of the above-described problems, and its purpose is to prevent the tip edge line portion of the elastic member from curling and wearing in a cleaning blade having a hardened contact portion with a member to be cleaned, It is an object of the present invention to provide a cleaning blade that can maintain good cleaning properties for a long period of time.

In order to achieve the above object, the present invention comprises a strip-shaped elastic member, abuts against the surface of the member to be cleaned that moves the surface of the tip ridge line portion of the elastic member, and adheres to the surface of the member to be cleaned. In the cleaning blade for removing deposits, the ultraviolet curable composition containing a (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule of the contact portion of the elastic member with the surface of the member to be cleaned has a modified layer comprising a cured product of the composition, wherein the elastic member reforming repulsion in the portion other than the layer elastic Ri 72% der than 36% or more at 23 ° C., having 6 or more carbons in the molecule The (meth) acrylate compound having an alicyclic structure is at least one selected from a (meth) acrylate compound having a tricyclodecane structure and a (meth) acrylate compound having an adamantane structure And characterized in that.

  According to the present invention, in a cleaning blade whose contact portion with a member to be cleaned has a high hardness, the tip ridge line portion of the elastic member is prevented from curling and wearing, and good cleaning properties are maintained over a long period of time. Can do.

The perspective view of the cleaning blade of this embodiment. 1 is a schematic configuration diagram illustrating an example of an image forming apparatus according to an exemplary embodiment. 1 is a schematic configuration diagram of an image forming unit in an example of an image forming apparatus according to an embodiment. (A) is an enlarged sectional view showing a state in which the cleaning blade is in contact with the surface of the photoreceptor. (B) is an enlarged view of the vicinity of the edge portion of the cleaning blade. (A) And (b) is explanatory drawing for demonstrating the measuring method of the circularity of a toner. The schematic diagram which showed the measurement location of abrasion of the cleaning blade in an Example. (A) is a figure which shows the state where the front-end ridgeline part of the conventional cleaning blade was curled. (B) is a figure explaining the local abrasion of the front end surface of the conventional cleaning blade. (C) is a figure which shows the state which the front-end ridgeline part of the conventional cleaning blade was missing.

Hereinafter, an embodiment of a cleaning blade to which the present invention is applied will be described.
FIG. 1 is a perspective view of the cleaning blade of this embodiment.
The cleaning blade 62 of the present embodiment includes a strip-shaped elastic member 622, and includes a modified layer 62d for increasing the hardness of the tip ridge line portion 62c of the elastic member 622, and further supports the support member 621. Accordingly, other members are included. In the cleaning blade 62, one end of the elastic member 622 is connected to the support member 621, the other end has a free end portion having a predetermined length, and the tip ridge line portion 62c, which is one end on the free end side, is provided on the surface of the member to be cleaned It arrange | positions so that it may contact | abut to a longitudinal direction. Thereby, the deposit | attachment adhering to the said to-be-cleaned member surface is removed.

<To be cleaned>
The member to be cleaned is not particularly limited with respect to its material, shape, structure, size, etc., and can be appropriately selected according to the purpose. Examples of the shape of the member to be cleaned include a drum shape, a belt shape, a flat plate shape, and a sheet shape. There is no restriction | limiting in particular as a magnitude | size of the said member to be cleaned, Although it can select suitably according to the objective, The magnitude | size normally used is preferable.
There is no restriction | limiting in particular as a material of the said to-be-cleaned member, According to the objective, it can select suitably, A metal, a plastic, a ceramic, etc. are mentioned.
There is no restriction | limiting in particular as said member to be cleaned, According to the objective, it can select suitably, For example, when the said cleaning blade is applied to an image forming apparatus, an image carrier etc. are mentioned.

<Adherent>
The adhering matter is not particularly limited as long as it adheres to the surface of the member to be cleaned and is a removal target of the cleaning blade, and can be appropriately selected according to the purpose. For example, toner, lubricant, inorganic fine particles, organic fine particles, dust, dust, or a mixture thereof can be used.

<Supporting member>
The support member 621 is not particularly limited in shape, size, material, and the like, and can be appropriately selected depending on the purpose. Examples of the shape of the support member 621 include a flat plate shape, a strip shape, and a sheet shape. There is no restriction | limiting in particular as a magnitude | size of the said supporting member 621, According to the magnitude | size of the said member to be cleaned, it can select suitably.
Examples of the material of the support member 621 include metals, plastics, and ceramics. Among these, a metal plate is preferable from the viewpoint of strength, and a steel plate such as stainless steel, an aluminum plate, and a phosphor bronze plate are particularly preferable.

<Elastic member>
There is no restriction | limiting in particular about the shape, material, magnitude | size, structure, etc. as said elastic member 622, According to the objective, it can select suitably. The elastic member 622 may have a strip shape. There is no restriction | limiting in particular as a magnitude | size of the said elastic member, According to the magnitude | size of the said member to be cleaned, it can select suitably.
There is no restriction | limiting in particular as a material of the said elastic member 622, Although it can select suitably according to the objective, Polyurethane rubber, a polyurethane elastomer, etc. are suitable from the point which is easy to obtain high elasticity.

  The elastic member 622 is not particularly limited and can be appropriately selected depending on the purpose. For example, a polyurethane prepolymer is prepared using a polyol compound and a polyisocyanate compound, a curing agent and, if necessary, a curing catalyst are added to the polyurethane prepolymer, crosslinked in a predetermined mold, and placed in a furnace. And post-crosslink. This is manufactured by forming into a sheet form by centrifugal molding, leaving it at room temperature and aging, and then cutting it into a flat plate shape with a predetermined dimension.

There is no restriction | limiting in particular as said polyol compound, According to the objective, it can select suitably, For example, high molecular weight polyol, low molecular weight polyol, etc. are mentioned.
Examples of the high molecular weight polyol include a polyester polyol which is a condensate of an alkylene glycol and an aliphatic dibasic acid; ethylene adipate ester polyol, butylene adipate ester polyol, hexylene adipate ester polyol, ethylene propylene adipate ester polyol, ethylene butylene Polyester polyols such as polyester polyols of alkylene glycol and adipic acid such as adipate ester polyol and ethylene neopentylene adipate ester polyol; polycaprolactone polyols such as polycaprolactone ester polyol obtained by ring-opening polymerization of caprolactone; Polyethers such as oxytetramethylene) glycol and poly (oxypropylene) glycol Polyol, and the like. These may be used individually by 1 type and may use 2 or more types together.

  Examples of the low molecular weight polyol include 1,4-butanediol, ethylene glycol, neopentyl glycol, hydroquinone-bis (2-hydroxyethyl) ether, and 3,3′-dichloro-4,4′-diaminodiphenylmethane. Dihydric alcohols such as 4,4′-diaminodiphenylmethane; 1,1,1-trimethylolpropane, glycerin, 1,2,6-hexanetriol, 1,2,4-butanetriol, trimethylolethane, Examples thereof include trivalent or higher polyhydric alcohols such as 1,1,1-tris (hydroxyethoxymethyl) propane, diglycerin, and pentaerythritol. These may be used individually by 1 type and may use 2 or more types together.

There is no restriction | limiting in particular as said polyisocyanate compound, According to the objective, it can select suitably, For example, a methylene diphenyl diisocyanate (MDI), tolylene diisocyanate (TDI), xylylene diisocyanate (XDI), naphthylene 1,5 Diisocyanate (NDI), tetramethylxylene diisocyanate (TMXDI), isophorone diisocyanate (IPDI), hydrogenated xylylene diisocyanate (H ₆ XDI), dicyclohexylmethane diisocyanate (H ₁₂ MDI), hexamethylene diisocyanate (HDI), dimer acid diisocyanate (DDI), norbornene diisocyanate (NBDI), trimethylhexamethylene diisocyanate (TMDI), and the like. These may be used individually by 1 type and may use 2 or more types together.

The curing catalyst is not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include 2-methylimidazole and 1,2-dimethylimidazole.
The content of the curing catalyst is not particularly limited and may be appropriately selected depending on the intended purpose, but is preferably 0.01% by mass to 0.5% by mass, and 0.05% by mass to 0.3% by mass. Is more preferable.

The JIS-A hardness of the elastic member 622 is not particularly limited and may be appropriately selected depending on the intended purpose, but is preferably 60 degrees or more, and more preferably 65 degrees to 80 degrees. When the JIS-A hardness is less than 60 degrees, it is difficult to obtain the blade linear pressure, and the area of the contact portion with the member to be cleaned is likely to be enlarged.
The elastic member 622 is not particularly limited and may be appropriately selected depending on the purpose. However, it is possible to use a laminate in which two or more kinds of rubbers having different JIS-A hardness are integrally formed. It is preferable at the point which can follow simultaneously.
Here, the JIS-A hardness of the elastic member 622 can be measured using, for example, a micro rubber hardness meter MD-1 manufactured by Kobunshi Keiki Co., Ltd.

The elastic resilience of the elastic member 622 based on the JIS K6255 standard is 36% or more and 72% or less at 23 ° C. Moreover, it is preferably 52% or more and 72% or less. If the rebound resilience is less than 36%, the flexibility of the entire elastic member is lost, and it becomes impossible to follow the vibration of the member to be cleaned and the roughness of the surface of the member to be cleaned, resulting in poor cleaning. On the other hand, if the rebound resilience exceeds 72%, the rebound is generally too strong and blade squealing occurs.
Here, the rebound resilience coefficient of the elastic member 622 is, for example, No. manufactured by Toyo Seiki Seisakusho Co., Ltd. at 23 ° C. in accordance with JIS K6255 standard. It can be measured using a 221 resilience tester.
There is no restriction | limiting in particular in the average thickness of the said elastic member, Although it can select suitably according to the objective, 1.0 mm-3.0 mm are preferable.

<Modified layer>
The tip ridge line part (contact part) 62c that contacts the surface of the member to be cleaned of the elastic member 622 contains a (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule. Contains a cured product.
The “contact portion includes a cured product of an ultraviolet curable composition containing a (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule” means that the tip ridge portion (contact portion) ) It may be included not only on the surface of 62c but also inside, and when a surface layer is formed on the tip ridge line portion (contact portion) 62c, it is included inside the tip ridge line portion (contact portion) 62c. And a case where a surface layer is formed at the contact portion.
In addition, if at least the tip ridge line portion (contact portion) 62c of the elastic member 622 contains a cured product of the ultraviolet curable composition, the ultraviolet curable composition is also applied to portions other than the contact portion of the elastic member. The cured product may be included.

<< UV curable composition >>
The ultraviolet curable composition contains a (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule, and further contains other components as necessary.

-(Meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule-
Since the (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule has a bulky special alicyclic structure in the molecule, the number of functional groups is small and the molecular weight is small (meth). Since an acrylate compound can be used, the tip ridge line portion 62c of the elastic member 622 can be easily impregnated, and the hardness of the tip ridge line portion 62c can be improved efficiently. Further, when a surface layer is provided on the tip ridge line portion 62c, the surface layer can be prevented from being cracked or peeled off.

6-12 are preferable and, as for carbon number of the alicyclic structure of the (meth) acrylate compound which has a C6 or more alicyclic structure in the said molecule | numerator, 8-10 are more preferable. If the number of carbon atoms is less than 6, the hardness of the contact portion may be weakened, and if it exceeds 12, steric hindrance may occur.
The number of functional groups of the (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule is preferably 2 to 6, and more preferably 2 to 4. If the number of functional groups is less than 2, the acrylic group can be bonded only on one side, and a bonding network cannot be formed, and the hardness of the tip ridge line portion (contact portion) 62c may be weakened. On the other hand, when the number of the functional groups exceeds 6, the acrylic groups are too many to bond with each other, and steric hindrance may occur.
The molecular weight of the (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule is preferably 450 or less. When the molecular weight exceeds 450, the molecular size increases, so that it is difficult to impregnate the elastic member, and it may be difficult to increase the hardness.

  As the (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule, a tricyclodecane structure can be used because a shortage of crosslinking points can be compensated by a special cyclic structure even if there are few functional groups. At least one selected from a (meth) acrylate compound having an adamantane structure and a (meth) acrylate compound having an adamantane structure is preferable.

The (meth) acrylate compound having a tricyclodecane structure is not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include tricyclodecane dimethanol diacrylate and tricyclodecane dimethanol dimethacrylate. Is mentioned.
As the (meth) acrylate compound having the tricyclodecane structure, an appropriately synthesized compound or a commercially available product may be used. As this commercial item, brand name: A-DCP (made by Shin-Nakamura Chemical Co., Ltd.) etc. are mentioned, for example.

The (meth) acrylate compound having an adamantane structure is not particularly limited and may be appropriately selected depending on the intended purpose. For example, 1,3-adamantane dimethanol diacrylate, 1,3-adamantane dimethanol dimethacrylate 1,3,5-adamantane trimethanol triacrylate, 1,3,5-adamantane trimethanol trimethacrylate, and the like.
As the (meth) acrylate compound having an adamantane structure, an appropriately synthesized one or a commercially available product may be used. As this commercial item, a brand name: X-DA (made by Idemitsu Kosan Co., Ltd.), a brand name: X-A-201 (made by Idemitsu Kosan Co., Ltd.), a brand name: ADTM (made by Mitsubishi Gas Chemical Co., Ltd.) , Etc.

The content of the (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule is not particularly limited and may be appropriately selected depending on the intended purpose. 20 mass%-100 mass% are preferable, and 50 mass%-100 mass% are more preferable. When the content is less than 20% by mass, high hardness due to a special cyclic structure may be impaired.
The (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule (in particular, a (meth) acrylate compound having a tricyclodecane structure or a (meth) acrylate compound having an adamantane structure) is preferable. It can be analyzed by, for example, an infrared microscope or liquid chromatography that the elastic member 622 is included in the tip ridge line portion 62c that contacts the surface of the member to be cleaned.

The ultraviolet curable composition may contain a (meth) acrylate compound having a molecular weight of 100 to 1,500 in addition to the (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule. .
The (meth) acrylate compound having a molecular weight of 100 to 1,500 is not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include dipentaerythritol hexa (meth) acrylate and pentaerythritol tetra (meth). Acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol ethoxytetra (meth) acrylate, trimethylolpropane tri (meth) acrylate, trimethylolpropane ethoxytri (meth) acrylate, 1,6-hexanediol di (meth) acrylate, Ethoxylated bisphenol A di (meth) acrylate, propoxylated ethoxylated bisphenol A di (meth) acrylate, 1,4-butanediol di (meth) acrylate, 1,5-pentanediol di ( Acrylate), 1,6-hexanediol di (meth) acrylate, 1,7-heptanediol di (meth) acrylate, 1,8-octanediol di (meth) acrylate, 1,9-nonanediol di (meth) Acrylate, 1,10-decanediol di (meth) acrylate, 1,11-undecanediol di (meth) acrylate, 1,18-octadecanediol di (meth) acrylate, glycerin propoxytri (meth) acrylate, dipropylene glycol di (Meth) acrylate, tripropylene glycol di (meth) acrylate, PO-modified neopentyl glycol di (meth) acrylate, PEG600 di (meth) acrylate, PEG400 di (meth) acrylate, PEG200 di (meth) acrylate, Opentyl glycol hydroxypivalate ester di (meth) acrylate, octyl / decyl (meth) acrylate, isobornyl (meth) acrylate, ethoxylated phenyl (meth) acrylate, 9,9-bis [4- (2- (meth) acryloyl) Oxyethoxy) phenyl] fluorene, and the like. These may be used individually by 1 type and may use 2 or more types together. Among these, a compound having a pentaerythritol triacrylate structure having 3 to 6 functional groups is preferable.
Examples of the compound having a pentaerythritol triacrylate structure having 3 to 6 functional groups include pentaerythritol triacrylate and dipentaerythritol hexaacrylate.

<Other ingredients>
There is no restriction | limiting in particular as said other component, According to the objective, it can select suitably, For example, a photoinitiator, a polymerization inhibitor, a diluent, etc. are mentioned.

-Photopolymerization initiator-
The photopolymerization initiator is not particularly limited as long as it generates active species such as radicals and cations by light energy and initiates polymerization, and can be appropriately selected according to the purpose. A radical polymerization initiator, a photocationic polymerization initiator, etc. are mentioned. Among these, a photo radical polymerization initiator is particularly preferable.

  Examples of the radical photopolymerization initiator include aromatic ketones, acylphosphine oxide compounds, aromatic onium salt compounds, organic peroxides, thio compounds (thioxanthone compounds, thiophenyl group-containing compounds, etc.), hexaarylbiimidazoles, and the like. Examples thereof include compounds, ketoxime ester compounds, borate compounds, azinium compounds, metallocene compounds, active ester compounds, compounds having a carbon halogen bond, and alkylamine compounds.

  The radical photopolymerization initiator is not particularly limited and may be appropriately selected depending on the intended purpose. For example, acetophenone, acetophenone benzyl ketal, 1-hydroxycyclohexyl phenyl ketone, 2,2-dimethoxy-2-phenylacetophenone , Xanthone, fluorenone, benzaldehyde, fluorene, anthraquinone, triphenylamine, carbazole, 3-methylacetophenone, 4-chlorobenzophenone, 4,4'-dimethoxybenzophenone, 4,4'-diaminobenzophenone, Michler's ketone, benzoin propyl ether , Benzoin ethyl ether, benzyldimethyl ketal, 1- (4-isopropylphenyl) -2-hydroxy-2-methylpropan-1-one, 2-hydroxy-2-methyl-1 Phenylpropan-1-one, thioxanthone, diethylthioxanthone, 2-isopropylthioxanthone, 2-chlorothioxanthone, 2-methyl-1- [4- (methylthio) phenyl] -2-morpholino-propan-1-one, bis (2 , 4,6-trimethylbenzoyl) -phenylphosphine oxide, 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide, 2,4-diethylthioxanthone, bis- (2,6-dimethoxybenzoyl) -2,4 , 4-trimethylpentylphosphine oxide, and the like. These may be used individually by 1 type and may use 2 or more types together.

  Commercially available products can be used as the photoradical polymerization initiator. Examples of the commercially available products include Irgacure 651, Irgacure 184, DAROCUR 1173, Irgacure 2959, Irgacure 127, Irgacure 907, Irgacure 369, Irgacure 379, and DAROCUR. TPO, IRGACURE 819, IRGACURE 784, IRGACURE OXE 01, IRGACURE OXE 02, IRGACURE 754 (above, manufactured by Ciba Specialty Chemicals); Speedcure TPO (manufactured by Lambson); KAYACURE DETX-S Co., Ltd. Lucirin TPO, LR 8893, LR 8970 (above, manufactured by BASF); Ubekrill P36 (manufactured by UCB), etc. It is below. These may be used individually by 1 type and may use 2 or more types together.

  The content of the photopolymerization initiator is not particularly limited and may be appropriately selected depending on the intended purpose, but is preferably 1% by mass to 20% by mass with respect to the ultraviolet curable composition.

-Polymerization inhibitor-
The polymerization inhibitor is not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include p-methoxyphenol, cresol, t-butylcatechol, di-t-butylparacresol, hydroquinone monomethyl ether, α Naphthol, 3,5-di-tert-butyl-4-hydroxytoluene, 2,2'-methylenebis (4-methyl-6-tert-butylphenol), 2,2'-methylenebis (4-ethyl-6-butylphenol) ), 4,4′-thiobis (3-methyl-6-t-butylphenol); p-benzoquinone, anthraquinone, naphthoquinone, phenanthraquinone, p-xyloquinone, p-toluquinone, 2,6-dichloro Quinone, 2,5-diphenyl-p-benzoquinone, 2,5-diacetoxy-p-benzox 2,5-dicaproxy-p-benzoquinone, 2,5-diacyloxy-p-benzoquinone, hydroquinone, 2,5-di-butylhydroquinone, mono-t-butylhydroquinone, monomethylhydroquinone, 2,5-di-t A quinone compound such as amylhydroquinone; an amine compound such as phenyl-β-naphthylamine, p-benzylaminophenol, di-β-naphthylparaphenylenediamine, dibenzylhydroxylamine, phenylhydroxylamine, diethylhydroxylamine; Nitro compounds such as nitrotoluene and picric acid; oxime compounds such as quinone dioxime and cyclohexanone oxime; and sulfur compounds such as phenothiazine. These may be used individually by 1 type and may use 2 or more types together.

-Diluent-
The diluent is not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include hydrocarbon solvents such as toluene and xylene; ethyl acetate, n-butyl acetate, methyl cellosolve acetate, propylene glycol monomethyl ether Ester solvents such as acetate; ketone solvents such as methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, cyclohexanone, cyclopentanone; ether solvents such as ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, propylene glycol monomethyl ether; ethanol, Examples thereof include alcohol solvents such as propanol, 1-butanol, isopropyl alcohol, and isobutyl alcohol. These may be used individually by 1 type and may use 2 or more types together.

As a method of including the cured product of the ultraviolet curable composition containing the (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule in the tip ridge line portion 62c of the elastic member 622, there is a particular limitation. For example, (1) after impregnating the ultraviolet curable composition into the tip ridge line portion 62c of the elastic member 622 by brushing, dip coating or the like, (2) The tip ridge line portion 62c of the elastic member 622 is coated with an ultraviolet curable composition by brushing, impregnating by dip coating, and the like, and then the tip ridge line portion 62c is ultraviolet curable composition. A method of spraying an object to form a surface layer and irradiating and curing ultraviolet rays; (3) an ultraviolet curable composition is applied to the tip ridge line portion 62c of the elastic member 622 by brushing, dip coating or the like. After ultraviolet irradiation and cured, after which a method of forming a surface layer by spray coating an ultraviolet curable composition to the edge line 62c, and the like. Among these, the method (1) is preferable.
The irradiation condition of the ultraviolet rays is not particularly limited and may be appropriately selected depending on the purpose, integrated light quantity preferable ^{500mJ / cm 2 ~5,000mJ / cm 2} .

  A (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule (in particular, a (meth) acrylate compound having a tricyclodecane structure or an adamantane structure (meta ) An acrylate compound is preferable.) By including a cured product of an ultraviolet curable composition containing), the tip ridge line portion 62c of the elastic member is increased in hardness, and the tip ridge line portion 62c is bent or deformed. Can be suppressed. Further, even when the inside is exposed due to wear of the tip ridge line portion 62c with time, the dripping and deformation can be similarly suppressed by the impregnation action.

  The cleaning blade 62 of the present invention can suppress the curl and wear of the tip ridge line portion 62c that contacts the surface of the member to be cleaned of the elastic member, and can maintain a good cleaning property for a long period of time. For this reason, it can be widely used in various fields, but it is particularly suitably used for the image forming apparatus, the image forming method, and the process cartridge of the present invention described below.

(Image forming apparatus and image forming method)
The image forming apparatus of the present invention comprises at least an image carrier, a charging unit, an exposure unit, a developing unit, a transfer unit, a fixing unit, and a cleaning unit, and further appropriately selected as necessary. Other means. The charging unit and the exposure unit may be collectively referred to as an electrostatic latent image forming unit.

  The image forming method used in the present invention includes at least a charging step, an exposure step, a development step, a transfer step, a fixing step, and a cleaning step, and further includes other steps appropriately selected as necessary. It becomes. The charging process and the exposure process may be collectively referred to as an electrostatic latent image forming process.

  The image forming method used in the present invention can be preferably implemented by the image forming apparatus of the present invention, the charging step can be performed by the charging unit, and the exposure step can be performed by the exposing unit. The developing step can be performed by the developing unit, the transferring step can be performed by the transferring unit, the fixing step can be performed by the fixing unit, and the cleaning step can be performed by the cleaning unit. The other steps can be performed by the other means.

<Image carrier>
The image carrier (hereinafter sometimes referred to as “electrophotographic photoreceptor” or “photoreceptor”) is not particularly limited in terms of material, shape, structure, size, etc., and is appropriately selected from known ones. can do. Examples of the shape of the image carrier include a drum shape and a belt shape. Examples of the material of the image carrier include inorganic photoreceptors such as amorphous silicon and selenium, and organic photoreceptors (OPC) such as polysilane and phthalopolymethine.

<Charging step and charging means>
The charging step is a step of charging the surface of the image carrier, and is performed by a charging unit.
The charging can be performed, for example, by applying a voltage to the surface of the image carrier using the charging unit.
The charging means is not particularly limited and may be appropriately selected depending on the purpose. For example, the charging means known per se provided with a conductive or semiconductive roller, brush, film, rubber blade, etc. And non-contact chargers using corona discharge such as corotrons and corotrons.

The shape of the charging means may take any form, such as a roller, a magnetic brush, or a fur brush, and can be selected according to the specifications and form of the electrophotographic image forming apparatus. When using a magnetic brush, the magnetic brush is composed of, for example, various ferrite particles such as Zn-Cu ferrite as a charging means, a non-magnetic conductive sleeve for supporting it, and a magnet roll included therein. . Or when using a brush, for example, as the material of the fur brush, a fur treated with carbon, copper sulfide, metal or metal oxide is used, and this is wound around a metal or other conductive core. Make it a charger by sticking.
The charger is not limited to the contact charger as described above, but has an advantage that an image forming apparatus in which ozone generated from the charger is reduced can be obtained.
It is preferable that the charger is arranged in contact or non-contact with the image carrier and charges the surface of the image carrier by applying a direct current and an alternating voltage.
In addition, there is a charging roller in which a charging roller having a gap tape on the image carrier and arranged in a non-contact manner and charging the surface of the image carrier by applying a direct current and an alternating voltage to the charging roller in a superimposed manner. preferable.

<Exposure process and exposure means>
The exposure step is a step of exposing the charged image carrier surface, and is performed by the exposure means.
The exposure can be performed, for example, by exposing the surface of the image carrier imagewise using the exposure unit.
The optical system in the exposure is roughly classified into an analog optical system and a digital optical system. The analog optical system is an optical system that projects a document directly onto an image carrier by an optical system, and the digital optical system receives image information as an electrical signal, converts this into an optical signal, and converts it into an electrophotographic photosensitive device. It is an optical system that exposes and forms a body.
The exposure means is not particularly limited as long as it can be exposed like an image to be formed on the surface of the image carrier charged by the charging means, and can be appropriately selected according to the purpose. Examples thereof include various exposure devices such as a copying optical system, a rod lens array system, a laser optical system, a liquid crystal shutter optical system, and an LED optical system.
In the present invention, an optical back side system in which imagewise exposure is performed from the back side of the image carrier may be adopted.

<Development process and development means>
The developing step is a step of developing the electrostatic latent image with the toner to form a visible image.
The visible image can be formed, for example, by developing the electrostatic latent image using the toner, and can be performed by the developing unit.
The developing unit is not particularly limited as long as it can be developed using, for example, the toner, and can be appropriately selected from known ones. For example, the developing unit stores the toner and forms the electrostatic latent image Preferable examples include those having at least a developing unit capable of applying the toner in contact or non-contact.

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

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

  The toner stored in the developing device may be a developer containing the toner, and the developer may be a one-component developer or a two-component developer.

-Toner-
The toner contains toner base particles and an external additive, and further contains other components as necessary.
The toner may be a monochrome toner or a color toner.
The toner base particles include at least a binder resin and a colorant and, if necessary, other components such as a release agent and a charge control agent.

---- Binder resin ---
The binder resin is not particularly limited and may be appropriately selected depending on the intended purpose. Polymer, styrene-propylene copolymer, styrene-vinyltoluene copolymer, styrene-methyl acrylate copolymer, styrene-ethyl acrylate copolymer, styrene-butyl acrylate copolymer, styrene-methyl methacrylate Copolymer, styrene-ethyl methacrylate copolymer, styrene-butyl methacrylate copolymer, styrene-α-chloromethyl methacrylate copolymer, styrene-acrylonitrile copolymer, styrene-vinyl methyl ether copolymer, Styrene-vinyl methyl ketone copolymer, styrene-butadiene Polymer, styrene-isoprene copolymer, styrene-maleic acid copolymer, styrene-maleic acid ester copolymer, polymethyl methacrylate, polybutyl methacrylate, polyvinyl chloride resin, polyvinyl acetate resin, polyethylene resin, Polypropylene resin, polyester resin, polyurethane resin, epoxy resin, polyvinyl butyral resin, polyacrylic acid resin, rosin, modified rosin, terpene resin, phenol resin, aliphatic hydrocarbon, aromatic petroleum resin, chlorinated paraffin, paraffin wax, Etc. These may be used individually by 1 type and may use 2 or more types together. Among these, polyester resins are particularly preferable in that the melt viscosity can be lowered while ensuring the stability during storage of the toner as compared with styrene resins and acrylic resins.

  The polyester resin can be obtained, for example, by a polycondensation reaction between an alcohol component and a carboxylic acid component.

  There is no restriction | limiting in particular as said alcohol component, According to the objective, it can select suitably, For example, polyethyleneglycol, diethyleneglycol, triethyleneglycol, 1,2-propyleneglycol, 1,3-propyleneglycol, 1,4 -Diols such as propylene glycol, neopentyl glycol, 1,4-butenediol; 1,4-bis (hydroxymethyl) cyclohexane, bisphenol A, hydrogenated bisphenol A, polyoxyethylenated bisphenol A, polyoxypropylenated bisphenol Etherified bisphenols such as A; divalent alcohol units in which these are substituted with a saturated or unsaturated hydrocarbon group having 3 to 22 carbon atoms; other divalent alcohol units; sorbitol, 1, 2, 3 , 6-Hexaneteto , 1,4-sorbitan, pentaesitol, dipentaerythritol, tripentaerythritol, sucrose, 1,2,4-butanetriol, 1,2,5-pentanetriol, glycerol, 2 -Trivalent or higher polyhydric alcohol monomers such as methylpropanetriol, 2-methyl-1,2,4-butanetriol, trimethylolethane, trimethylolpropane, 1,3,5-trihydroxymethylbenzene, etc. Is mentioned.

  The carboxylic acid component is not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include monocarboxylic acids such as palmitic acid, stearic acid, and oleic acid; maleic acid, fumaric acid, mesaconic acid, citraconic acid , Terephthalic acid, cyclohexanedicarboxylic acid, succinic acid, adipic acid, sebacic acid, malonic acid, divalent organic acid monomers in which these are substituted with a saturated or unsaturated hydrocarbon group having 3 to 22 carbon atoms, these Acid anhydride, lower alkyl ester and dimer acid from linolenic acid; 1,2,4-benzenetricarboxylic acid, 1,2,5-benzenetricarboxylic acid, 2,5,7-naphthalenetricarboxylic acid, 1 , 2,4-Naphthalenetricarboxylic acid, 1,2,4-butanetricarboxylic acid, 1,2,5-hexanetricarboxylic acid, 3,3-dicarbo Shimechirubutan acid, tetra carboxymethyl methane, 1,2,7,8-octane tetracarboxylic acid Enboru trimer acid, a trivalent or higher polycarboxylic acid monomers anhydrides of these acids, and the like.

--- Colorant ---
The colorant is not particularly limited and may be appropriately selected from known dyes and pigments according to the purpose. For example, carbon black, nigrosine dye, iron black, naphthol yellow S, Hansa yellow (10G, 5G, G), Cadmium yellow, Yellow iron oxide, Ocher, Yellow lead, Titanium yellow, Polyazo yellow, Oil yellow, Hansa yellow (GR, A, RN, R), Pigment yellow L, Benzidine yellow (G, GR) , Permanent Yellow (NCG), Vulcan Fast Yellow (5G, R), Tartrazine Lake, Quinoline Yellow Lake, Anthrazan Yellow BGL, Isoindolinone Yellow, Bengala, Red Dan, Lead Zhu, Cadmium Red, Cadmium Mercury Red, Antimony Zhu, Permanent Red 4R, Parallel , Faise red, parachlor ortho nitroaniline red, Resol Fast Scarlet G, Brilliant Fast Scarlet, Brilliant Carmine BS, Permanent Red (F2R, F4R, FRL, FRLL, F4RH), Fast Scarlet VD, Belkan Fast Rubin B, Brilliant Scarlet G, Risor Rubin GX, Permanent Red F5R, Brilliant Carmine 6B, Pigment Scarlet 3B, Bordeaux 5B, Toluidine Maroon, Permanent Bordeaux F2K, Helio Bordeaux BL, Bordeaux 10B, Bon Maroon Light, Bon Maroon Medium, Eosin Lake, Rhodamine Lake B , Rhodamine lake Y, alizarin lake, thioindigo red B, thioindigo maroon, oil Quinacridone red, pyrazolone red, polyazo red, chrome vermilion, benzidine orange, perinone orange, oil orange, cobalt blue, cerulean blue, alkaline blue rake, peacock blue rake, Victoria blue rake, metal-free phthalocyanine blue, phthalocyanine blue, Fast Sky Blue, Indanthrene Blue (RS, BC), Indigo, Ultramarine Blue, Bitumen, Anthraquinone Blue, Fast Violet B, Methyl Violet Lake, Cobalt Purple, Manganese Purple, Dioxane Violet, Anthraquinone Violet, Chrome Green, Zinc Green, Oxidation Chrome, Pyridian, Emerald Green, Pigment Green B, Naphthol Green B, Green Gold, Acid Guri And enamel lake, malachite green lake, phthalocyanine green, anthraquinone green, titanium oxide, zinc white, litbon, and the like. These may be used individually by 1 type and may use 2 or more types together.

  There is no restriction | limiting in particular as content in the said toner of the said coloring agent, Although it can select suitably according to the objective, 1 mass%-15 mass% are preferable, and 3 mass%-10 mass% are more preferable.

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

---- Release agent ---
There is no restriction | limiting in particular as said mold release agent, According to the objective, it can select suitably, For example, waxes etc. are mentioned.
Examples of the waxes include carbonyl group-containing waxes, polyolefin waxes, and long-chain hydrocarbons. These may be used individually by 1 type and may use 2 or more types together. Among these, a carbonyl group-containing wax is preferable.
Examples of the carbonyl group-containing wax include polyalkanoic acid esters, polyalkanol esters, polyalkanoic acid amides, polyalkylamides, dialkyl ketones, and the like. Examples of the polyalkanoic acid ester include carnauba wax, montan wax, trimethylolpropane tribehenate, pentaerythritol tetrabehenate, pentaerythritol diacetate dibehenate, glycerin tribehenate, and 1,18-octadecane. And diol distearate. Examples of the polyalkanol ester include tristearyl trimellitic acid, distearyl maleate, and the like. Examples of the polyalkanoic acid amide include dibehenyl amide. Examples of the polyalkylamide include trimellitic acid tristearylamide. Examples of the dialkyl ketone include distearyl ketone. Among these carbonyl group-containing waxes, polyalkanoic acid esters are particularly preferable.
Examples of the polyolefin wax include polyethylene wax and polypropylene wax.
Examples of the long chain hydrocarbon include paraffin wax and sazol wax.
The content of the release agent in the toner is not particularly limited and may be appropriately selected depending on the intended purpose, but is preferably 5% by mass to 15% by mass.

---- Charge control agent ---
The charge control agent is not particularly limited and may be appropriately selected depending on the intended purpose.For example, nigrosine dyes, triphenylmethane dyes, chromium-containing metal complex dyes, molybdate chelate pigments, rhodamine dyes, Alkoxy amines, quaternary ammonium salts (including fluorine-modified quaternary ammonium salts), alkylamides, phosphorus simple substances or compounds, tungsten simple substances or compounds, fluorine activators, salicylic acid metal salts, metal salts of salicylic acid derivatives, etc. Can be mentioned.

  The content of the charge control agent is not particularly limited and may be appropriately selected depending on the intended purpose, but is preferably 0.1 parts by mass to 10 parts by mass with respect to 100 parts by mass of the toner. 2 mass parts-5 mass parts are more preferable.

--External additive--
The external additive is not particularly limited as long as it contains at least silica particles, and can be appropriately selected according to the purpose. Also, for example, inorganic particles such as silica, titanium oxide, alumina, silicon carbide, silicon nitride, boron nitride; polymethyl methacrylate particles and polystyrene particles having an average particle size of 0.05 μm to 1 μm obtained by a soap-free emulsion polymerization method Such resin particles may be included. These may be used individually by 1 type and may use 2 or more types together. Among these, silica whose surface is hydrophobized is particularly preferable.

Examples of the silica include silicone-treated silica. The silicone-treated silica is silica whose surface has been surface-treated (hydrophobized) with silicone oil.
The surface treatment method is not particularly limited and can be appropriately selected depending on the purpose.
Examples of the silicone oil include dimethyl silicone oil, methyl hydrogen silicone oil, and methylphenyl silicone oil.
A commercially available product can be used as the silicone-treated silica. As said commercial item, RY200, R2T200S, NY50, RY50 (above, Nippon Aerosil Co., Ltd. product) etc. are mentioned, for example.

-Other ingredients-
The other components in the toner are not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include a fluidity improver, a cleaning improver, a magnetic material, and a metal soap.

The fluidity improver can be surface-treated to increase hydrophobicity and prevent deterioration of fluidity and charging characteristics even under high humidity. For example, a silane coupling agent, a silylating agent, and a fluoride can be used. Examples thereof include silane coupling agents having an alkyl group, organic titanate coupling agents, aluminum coupling agents, silicone oils, and modified silicone oils.
The cleaning property improver is added to the toner in order to remove the toner after transfer remaining on the image carrier or intermediate transfer member. For example, a fatty acid metal salt such as zinc stearate, calcium stearate, stearic acid; Examples thereof include polymer fine particles produced by soap-free emulsion polymerization such as methyl methacrylate fine particles and polystyrene fine particles. The polymer fine particles preferably have a relatively narrow particle size distribution, and those having a volume average particle size of 0.01 μm to 1 μm are suitable.
There is no restriction | limiting in particular as said magnetic material, According to the objective, it can select suitably, For example, iron powder, magnetite, a ferrite, etc. are mentioned. Among these, white is preferable in terms of color tone.

--Method of manufacturing toner--
The method for producing the toner is not particularly limited, and can be appropriately selected from conventionally known toner production methods according to the purpose. Examples thereof include a kneading / pulverizing method, a polymerization method, a dissolution suspension method, and a spraying method. Granulation method and the like. Among these, in order to improve the image quality, a polymerization method such as a suspension polymerization method, an emulsion polymerization method, or a dispersion polymerization method, which can easily increase the circularity and reduce the particle size, is preferable.

---- Kneading and grinding method ---
The kneading and pulverizing method is, for example, a method of manufacturing the toner base particles by melt-kneading a toner material containing at least a binder resin and a colorant, pulverizing and classifying the obtained kneaded material. is there.
In the melt kneading, the toner materials are mixed, and the mixture is charged into a melt kneader and melt kneaded. As the melt kneader, for example, a uniaxial or biaxial continuous kneader or a batch kneader using a roll mill can be used. For example, a KTK type twin screw extruder manufactured by Kobe Steel, a TEM type extruder manufactured by Toshiba Machine Co., Ltd., a twin screw extruder manufactured by Casey Kay, a PCM type twin screw extruder manufactured by Ikegai Iron Works, a Kneader manufactured by Buss, etc. are suitable. Used for. This melt-kneading is preferably performed under appropriate conditions so as not to cause the molecular chains of the binder resin to be broken. Specifically, the melt-kneading temperature is determined with reference to the softening point of the binder resin. If the temperature is higher than the softening point, cutting is severe, and if the temperature is too low, dispersion may not proceed.

  In the pulverization, the kneaded material obtained by the melt-kneading is pulverized. In this pulverization, it is preferable that the kneaded material is first coarsely pulverized and then finely pulverized. At this time, a method of pulverizing by colliding with a collision plate in a jet stream, pulverizing particles by colliding with each other in a jet stream, or pulverizing with a narrow gap between a rotor and a stator that rotate mechanically is preferably used. .

In the classification, the pulverized product obtained by the pulverization is classified and adjusted to particles having a predetermined particle diameter. The classification can be performed, for example, by removing the fine particle portion with a cyclone, a decanter, a centrifuge, or the like.
After the pulverization and classification are completed, the pulverized product is classified into an air stream by centrifugal force or the like, and toner base particles having a predetermined particle diameter can be produced.

  Next, the external additive is externally added to the toner base particles. By mixing and stirring the toner base particles and the external additive using a mixer, the surface of the toner base particles is coated while being crushed. At this time, it is important in terms of durability that the external additive such as silica particles is uniformly and firmly attached to the toner base particles.

--- Polymerization method ---
As a method for producing a toner by the polymerization method, for example, a toner material containing a modified polyester resin capable of at least urea or urethane bond and a colorant is dissolved or dispersed in an organic solvent. Then, this dissolved or dispersed material is dispersed in an aqueous medium, subjected to a polyaddition reaction, and the solvent of this dispersion is removed and washed.

  Examples of the modified polyester resin capable of being bonded with urea or urethane include, for example, a polyester prepolymer having an isocyanate group, obtained by reacting a carboxyl group or a hydroxyl group at the terminal of a polyester with a polyvalent isocyanate compound (PIC). Etc. The modified polyester resin obtained by crosslinking and / or extending the molecular chain by the reaction of this polyester prepolymer and amines can improve the hot offset property while maintaining the low temperature fixability.

Examples of the polyvalent isocyanate compound (PIC) include aliphatic polyisocyanates (for example, tetramethylene diisocyanate, hexamethylene diisocyanate, 2,6-diisocyanatomethyl caproate); alicyclic polyisocyanates (for example, Isophorone diisocyanate, cyclohexylmethane diisocyanate, etc.); aromatic diisocyanate (eg, tolylene diisocyanate, diphenylmethane diisocyanate, etc.); aromatic aliphatic diisocyanate (eg, α, α, α ′, α′-tetramethylxylylene diisocyanate, etc.); And those obtained by blocking the polyisocyanate with a phenol derivative, oxime, caprolactam or the like. These may be used individually by 1 type and may use 2 or more types together.
The ratio of the polyvalent isocyanate compound (PIC) is not particularly limited and may be appropriately selected depending on the intended purpose. ] / [OH] is preferably 5/1 to 1/1, more preferably 4/1 to 1.2 / 1, and still more preferably 2.5 / 1 to 1.5 / 1.

  The isocyanate group contained per molecule in the polyester prepolymer (A) having an isocyanate group is not particularly limited and may be appropriately selected depending on the intended purpose. 5 to 3 is more preferable, and an average of 1.8 to 2.5 is more preferable.

Examples of amines (B) to be reacted with the polyester prepolymer include divalent amine compounds (B1), trivalent or higher polyvalent amine compounds (B2), amino alcohols (B3), amino mercaptans (B4), and amino acids. (B5), and those obtained by blocking the amino groups of B1 to B5 (B6).
Examples of the divalent amine compound (B1) include aromatic diamines (eg, phenylenediamine, diethyltoluenediamine, 4,4′-diaminodiphenylmethane); alicyclic diamines (eg, 4,4′-diamino-). 3,3′-dimethyldicyclohexylmethane, diaminecyclohexane, isophoronediamine, etc.); aliphatic diamines (eg, ethylenediamine, tetramethylenediamine, hexamethylenediamine, etc.), and the like.
Examples of the trivalent or higher polyvalent amine compound (B2) include diethylenetriamine and triethylenetetramine.
Examples of the amino alcohol (B3) include ethanolamine and hydroxyethylaniline.
Examples of the amino mercaptan (B4) include aminoethyl mercaptan and aminopropyl mercaptan.
Examples of the amino acid (B5) include aminopropionic acid and aminocaproic acid.
Examples of the blocked B1-B5 amino group (B6) include ketimine compounds and oxazolidine compounds obtained from the amines of B1-B5 and ketones (for example, acetone, methyl ethyl ketone, methyl isobutyl ketone, etc.) Is mentioned. Among these amines (B), B1 and a mixture of B1 and a small amount of B2 are particularly preferable.

  The ratio of the amines (B) is not particularly limited and may be appropriately selected depending on the intended purpose. The isocyanate group [NCO] in the polyester prepolymer (A) having an isocyanate group and the amines (B The equivalent ratio [NCO] / [NHx] of the amino group [NHx] is preferably 1/2 to 2/1, more preferably 1.5 / 1 to 1 / 1.5, and 1.2 / 1. -1 / 1.2 is more preferable.

  According to the method for producing a toner by the polymerization method as described above, a toner having a small particle diameter and a spherical shape can be produced at low cost with little environmental load.

The disperser for the dispersion is not particularly limited and can be appropriately selected according to the purpose. For example, a low-speed shear disperser, a high-speed shear disperser, a friction disperser, and a high-pressure jet disperser. And an ultrasonic disperser.
Among these, a high-speed shearing disperser is preferable in that the particle size of the dispersion (oil droplets) can be controlled to 2 μm to 20 μm.
When the high-speed shearing disperser is used, conditions such as the number of rotations, the dispersion time, and the dispersion temperature can be appropriately selected according to the purpose.
There is no restriction | limiting in particular as said rotation speed, Although it can select suitably according to the objective, 1,000 rpm-30,000 rpm are preferable, and 5,000 rpm-20,000 rpm are more preferable.
There is no restriction | limiting in particular as said dispersion | distribution time, Although it can select suitably according to the objective, In the case of a batch system, 0.1 minute-5 minutes are preferable.
There is no restriction | limiting in particular as said dispersion | distribution temperature, Although it can select suitably according to the objective, 0 degreeC-150 degreeC is preferable under pressure, and 40 degreeC-98 degreeC is more preferable. In general, dispersion is easier when the dispersion temperature is higher.

  The amount of the aqueous medium used when the toner material is dispersed in the aqueous medium is not particularly limited and may be appropriately selected depending on the intended purpose, but is 50 masses per 100 mass parts of the toner material. Parts to 2,000 parts by mass are preferable, and 100 parts to 1,000 parts by mass are more preferable.

The method for removing the organic solvent from the dispersion is not particularly limited and may be appropriately selected according to the purpose. For example, the temperature of the entire reaction system is gradually raised to evaporate the organic solvent in the oil droplets. And a method of spraying the dispersion into a dry atmosphere to remove the organic solvent in the oil droplets.
When the organic solvent is removed, toner base particles are formed. The toner base particles can be washed, dried, etc., and further classified. The classification may be performed by removing fine particle portions in a liquid by a cyclone, a decanter, centrifugation, or the like, or may be performed after drying.

The obtained toner base particles may be mixed with the external additive and, if necessary, particles such as the charge control agent. At this time, by applying a mechanical impact force, it is possible to prevent the particles such as the external additive from detaching from the surface of the toner base particles.
The method for applying the mechanical impact force is not particularly limited and can be appropriately selected depending on the purpose. For example, a method for applying the impact force to the mixture using blades rotating at high speed, For example, a method may be used in which the mixture is charged and accelerated to cause the particles or particles to collide with an appropriate collision plate.
There is no restriction | limiting in particular as an apparatus used for the said method, According to the objective, it can select suitably, For example, remodeling and grind | pulverizing an Ong mill (made by Hosokawa Micron Corporation) and an I type mill (made by Nippon Pneumatic Co., Ltd.) Examples include an apparatus in which the air pressure is lowered, a hybridization system (manufactured by Nara Machinery Co., Ltd.), a kryptron system (manufactured by Kawasaki Heavy Industries, Ltd.), and an automatic mortar.

The average circularity of the toner is not particularly limited and may be appropriately selected depending on the intended purpose, but is preferably 0.97 or more, more preferably 0.97 to 0.98. If the average circularity is less than 0.97, satisfactory transferability and high-quality images without dust may not be obtained.
The average circularity of the toner can be measured using, for example, a flow type particle image analyzer FPIA-1000 manufactured by Sysmex Corporation.

The volume average particle diameter of the toner is not particularly limited and may be appropriately selected depending on the intended purpose, but is preferably 5.5 μm or less.
There is no restriction | limiting in particular as ratio (Dv / Dn) of the said volume average particle diameter (Dv) and number average particle diameter (Dn), Although it can select suitably according to the objective, 1.00-1. 40 is preferred. The closer the ratio (Dv / Dn) is to 1.00, the sharper the particle size distribution. With such a toner having a small particle size and a narrow particle size distribution, the toner charge amount distribution is uniform, a high-quality image with little background fogging can be obtained, and the electrostatic transfer method has a high transfer rate. can do.

  The volume average particle size and particle size distribution of the toner are measured by, for example, Coulter Counter TA-II, Coulter Multisizer II (both manufactured by Coulter Co., Ltd.) and the like as a measurement device for the particle size distribution of toner particles by the Coulter Counter method. can do.

The toner can be mixed with a magnetic carrier and used as a two-component developer. In this case, the mass ratio of the carrier and the toner in the two-component developer is not particularly limited and can be appropriately selected according to the purpose. Part is preferred.
Examples of the magnetic carrier include iron powder, ferrite powder, magnetite powder, and magnetic resin carrier having a particle diameter of about 20 μm to 200 μm.
The coating resin is not particularly limited and may be appropriately selected depending on the intended purpose. For example, urea-formaldehyde resin, melamine resin, benzoguanamine resin, urea resin, polyamide resin, epoxy resin, polyvinyl and polyvinylidene resin , Halogenated olefin resins such as acrylic resin, polymethyl methacrylate resin, polyacrylonitrile resin, polyvinyl acetate resin, polyvinyl alcohol resin, polyvinyl butyral resin, polystyrene resin, styrene-acrylic copolymer resin, polyvinyl chloride; polyethylene terephthalate resin, Polyester resins such as polybutylene terephthalate resin; polycarbonate resins, polyethylene resins, polyvinyl fluoride resins, polyvinylidene fluoride resins, polytrifluoroethylene resins, polyester resins Hexafluoropropylene resin, copolymer of vinylidene fluoride and acrylic monomer, copolymer of vinylidene fluoride and vinyl fluoride, terpolymer of tetrafluoroethylene, vinylidene fluoride and non-fluorinated monomer And fluoroterpolymers such as silicone resins.
Furthermore, you may make conductive powder etc. contain in coating resin as needed. Examples of the conductive powder include metal powder, carbon black, titanium oxide, tin oxide, and zinc oxide.
These conductive powders preferably have an average particle diameter of 1 μm or less. When the average particle diameter exceeds 1 μm, it may be difficult to control electric resistance.
The toner can also be used as a one-component magnetic toner that does not use a carrier, or a non-magnetic toner.

<Transfer process and transfer means>
The transfer step is a step of transferring the visible image onto a recording medium. After the primary transfer of the visible image onto the intermediate transfer member using an intermediate transfer member, the visible image is transferred onto the recording medium. A primary transfer step of forming a composite transfer image by transferring a visible image onto an intermediate transfer body using two or more colors, preferably full color toner as the toner, and a composite transfer image; A mode including a secondary transfer step of transferring the transfer image onto the recording medium is more preferable.
The transfer can be performed, for example, by charging the image carrier with the visible image using a transfer unit, and can be performed by the transfer unit. The transfer means includes a primary transfer means for transferring a visible image onto an intermediate transfer member to form a composite transfer image, and a secondary transfer means for transferring the composite transfer image onto a recording medium. Embodiments are preferred.
The intermediate transfer member is not particularly limited and may be appropriately selected from known transfer members according to the purpose. Examples thereof include a transfer belt.

The transfer unit (the primary transfer unit and the secondary transfer unit) preferably includes at least a transfer unit that peels and charges the visible image formed on the image carrier to the recording medium side. . There may be one transfer means or two or more transfer means. Examples of the transfer device include a corona transfer device using corona discharge, a transfer belt, a transfer roller, a pressure transfer roller, and an adhesive transfer device.
The recording medium is typically plain paper, but is not particularly limited as long as it can transfer an unfixed image after development, and can be appropriately selected according to the purpose. A PET base or the like can also be used.

<Fixing process and fixing means>
The fixing step is a step of fixing the toner image transferred to the recording medium, and can be fixed using a fixing unit. When two or more color toners are used, the toner may be fixed each time the toner of each color is transferred to the recording medium, or the toner of all colors may be transferred to the recording medium and fixed in a stacked state. Also good. The fixing unit is not particularly limited, and a heat fixing method using a known heating and pressing unit can be employed. Examples of the heating and pressing means include a combination of a heating roller and a pressure roller, a combination of a heating roller, a pressure roller, and an endless belt. At this time, the heating temperature is not particularly limited and may be appropriately selected depending on the intended purpose, but is preferably 80 ° C to 200 ° C. If necessary, for example, a known optical fixing device may be used together with the fixing means.

<Cleaning process and cleaning means>
The cleaning step is a step of removing the toner remaining on the image carrier and can be suitably performed by a cleaning unit.
As the cleaning means, the cleaning blade of the present invention is used.
The elastic member of the cleaning blade is not particularly limited and may be appropriately selected according to the purpose. However, it is preferable that the elastic member is in contact with the surface of the image carrier with a pressing force of 10 N / m to 100 N / m. . When the pressing force is less than 10 N / m, a cleaning failure due to the passage of toner at the contact portion where the elastic member of the cleaning blade contacts the surface of the image carrier is likely to occur. The cleaning blade may be swung up due to an increase in the frictional force of the part. The pressing force is preferably 10 N / m to 50 N / m.
The pressing force can be measured using, for example, a measuring apparatus incorporating a small compression type load cell manufactured by Kyowa Denki Co., Ltd.

The angle formed between the tangent at the portion where the elastic member of the cleaning blade abuts on the surface of the image carrier and the end face of the cleaning blade is not particularly limited and can be appropriately selected according to the purpose. It is preferable that the angle is not more than °.
When the angle θ formed is less than 65 °, the cleaning blade may be swung up, and when it exceeds 85 °, a cleaning failure may occur.

<Other processes and other means>
Examples of the other means include a static elimination means, a recycling means, and a control means.
Examples of the other processes include a static elimination process, a recycling process, and a control process.

-Static elimination process and static elimination means-
The neutralization step is a step of performing neutralization by applying a neutralization bias to the image carrier, and can be suitably performed by a neutralization unit.
The neutralization means is not particularly limited, and may be appropriately selected from known neutralizers as long as it can apply a neutralization bias to the image carrier. For example, a neutralization lamp or the like is preferable. It is done.

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

-Control process and control means-
The control step is a step of controlling each of the steps, and can be suitably performed by a control unit.
The control means is not particularly limited as long as the movement of each means can be controlled, and can be appropriately selected according to the purpose. Examples thereof include devices such as a sequencer and a computer.

Here, an example of the image forming apparatus of the present invention will be described with reference to the drawings.
FIG. 2 is a schematic configuration diagram showing an example of the image forming apparatus 500 of the present invention. The image forming apparatus 500 includes four image forming units 1Y, 1C, 1M, and 1K for yellow, magenta, cyan, and black (hereinafter sometimes referred to as Y, C, M, and K). These use Y, C, M, and K toners of different colors as image forming substances for forming an image, but the other configurations are the same.

Above the four image forming units 1, a transfer unit 60 including an intermediate transfer belt 14 as an intermediate transfer member is disposed. The toner images of the respective colors formed on the surfaces of the photoreceptors 3Y, 3C, 3M, and 3K included in the image forming units 1Y, 1C, 1M, and 1K, which will be described in detail later, are superimposed on the surface of the intermediate transfer belt. It is a configuration to be transferred.
Further, an optical writing unit 40 is disposed below the four image forming units 1. The optical writing unit 40 serving as a latent image forming unit irradiates the photoconductors 3Y, 3C, 3M, and 3K of the image forming units 1Y, 1C, 1M, and 1K with the laser light L emitted based on the image information. Thereby, electrostatic latent images for Y, C, M, and K are formed on the photoreceptors 3Y, 3C, 3M, and 3K. The optical writing unit 40 polarizes the laser light L emitted from the light source by the polygon mirror 41 that is rotationally driven by a motor, and passes the photosensitive members 3Y, 3C, 3M, and 3K through a plurality of optical lenses and mirrors. Is irradiated. Instead of the configuration described above, it is also possible to employ one that performs light scanning with an LED array.

  Below the optical writing unit 40, a first paper feed cassette 151 and a second paper feed cassette 152 are arranged to overlap in the vertical direction. In each of these paper feed cassettes, a plurality of recording media P are stored in a stack of sheets, and the top recording medium P includes a first paper feed roller 151a and a second paper feed. The rollers 152a are in contact with each other. When the first paper feed roller 151a is driven to rotate counterclockwise in FIG. 2 by driving means (not shown), the uppermost recording medium P in the first paper feed cassette 151 is vertically oriented on the right side of the cassette in FIG. The paper is discharged toward a paper feed path 153 disposed so as to extend to the front. Further, when the second paper feeding roller 152a is rotated counterclockwise in FIG. 2 by a driving means (not shown), the uppermost recording medium P in the second paper feeding cassette 152 is discharged toward the paper feeding path 153. Is done.

  A plurality of conveying roller pairs 154 are arranged in the paper feed path 153. The recording medium P sent to the paper feed path 153 is conveyed from the lower side to the upper side in FIG. 2 while being sandwiched between the rollers of the conveyance roller pair 154.

  A registration roller pair 55 is disposed at the downstream end of the paper feed path 153 in the transport direction. The registration roller pair 55 temporarily stops the rotation of both rollers as soon as the recording medium P sent from the conveying roller pair 154 is sandwiched between the rollers. Then, the recording medium P is sent out toward a secondary transfer nip described later at an appropriate timing.

FIG. 3 is a configuration diagram showing a schematic configuration of one of the four image forming units 1.
As shown in FIG. 3, the image forming unit 1 includes a drum-shaped photoconductor 3 as an image carrier. The photoconductor 3 has a drum shape, but may have a sheet shape or an endless belt shape.
Around the photoreceptor 3, a charging roller 4, a developing device 5, a primary transfer roller 7, a cleaning device 6, a lubricant application device 10, a static elimination lamp (not shown), and the like are disposed. The charging roller 4 is a charging member provided in a charging device as a charging unit, and the developing device 5 is a developing unit that converts a latent image formed on the surface of the photoreceptor 3 into a toner image. The primary transfer roller 7 is a primary transfer member provided in a primary transfer device as a primary transfer unit that transfers a toner image on the surface of the photoreceptor 3 to the intermediate transfer belt 14. The cleaning device 6 is a cleaning unit that cleans the toner remaining on the photoreceptor 3 after the toner image is transferred to the intermediate transfer belt 14. The lubricant application device 10 is a lubricant application unit that applies a lubricant onto the surface of the photoreceptor 3 after the cleaning device 6 performs cleaning. A neutralizing lamp (not shown) is a neutralizing unit that neutralizes the surface potential of the photoreceptor 3 after cleaning.

The charging roller 4 is arranged in a non-contact manner with a predetermined distance from the photoconductor 3, and charges the photoconductor 3 to a predetermined polarity and a predetermined potential. The surface of the photoreceptor 3 uniformly charged by the charging roller 4 is irradiated with laser light L from an optical writing unit 40 serving as a latent image forming unit based on image information, thereby forming an electrostatic latent image.
The developing device 5 has a developing roller 51 as a developer carrier. A developing bias is applied to the developing roller 51 from a power source (not shown). In the casing of the developing device 5, a supply screw 52 and a stirring screw 53 are provided for stirring the developer contained in the casing while conveying the developer in opposite directions. A doctor 54 for regulating the developer carried on the developing roller 51 is also provided. The toner in the developer stirred and conveyed by the two screws of the supply screw 52 and the stirring screw 53 is charged to a predetermined polarity. The developer is pumped up on the surface of the developing roller 51, and the pumped-up developer is regulated by the doctor 54, and the toner adheres to the latent image on the photoconductor 3 in the development area facing the photoconductor 3. .

The cleaning device 6 includes a fur brush 101, a cleaning blade 62, and the like. The cleaning blade 62 is in contact with the photoconductor 3 in the counter direction with respect to the surface movement direction of the photoconductor 3. Details of the cleaning blade 62 will be described later.
The lubricant application device 10 includes a solid lubricant 103, a lubricant pressure spring 103 a, and the like, and uses a fur brush 101 as an application brush for applying the solid lubricant 103 onto the photoreceptor 3. The solid lubricant 103 is held by the bracket 103b and is pressed toward the fur brush 101 by a lubricant pressurizing spring 103a. Then, the solid lubricant 103 is scraped by the fur brush 101 that rotates in the rotational direction with respect to the rotation direction of the photoconductor 3, and the lubricant is applied onto the photoconductor 3. By applying lubricant to the photoreceptor, the friction coefficient on the surface of the photoreceptor 3 is maintained at 0.2 or less during non-image formation.

  The charging device is a non-contact proximity arrangement system in which the charging roller 4 is brought close to the photosensitive member 3, and as the charging device, known devices such as a corotron, a scorotron, and a solid state charger (solid state charger) are known. A configuration can be used. Among these charging methods, the contact charging method or the non-contact proximity arrangement method is more desirable, and has advantages such as high charging efficiency, a small amount of ozone generation, and miniaturization of the apparatus.

The light source of the laser light L of the optical writing unit 40 and the light source such as a static elimination lamp include a fluorescent lamp, a tungsten lamp, a halogen lamp, a mercury lamp, a sodium lamp, a light emitting diode (LED), a semiconductor laser (LD), and an electroluminescence (EL). ) And other luminescent materials can be used.
In addition, various types of filters such as a sharp cut filter, a band pass filter, a near infrared cut filter, a dichroic filter, an interference filter, and a color temperature conversion filter can be used to irradiate only light in a desired wavelength range.
Among these light sources, light emitting diodes and semiconductor lasers are used favorably because they have high irradiation energy and long wavelength light of 600 nm to 800 nm.

  2 includes a belt cleaning unit 162, a first bracket 63, a second bracket 64, and the like in addition to the intermediate transfer belt 14. In addition, four primary transfer rollers 7Y, 7C, 7M, and 7K, a secondary transfer backup roller 66, a driving roller 67, an auxiliary roller 68, a tension roller 69, and the like are also provided. The intermediate transfer belt 14 is endlessly moved counterclockwise in FIG. 2 by the rotational driving of the driving roller 67 while being stretched around these eight roller members. The four primary transfer rollers 7Y, 7C, 7M, and 7K sandwich the intermediate transfer belt 14 that is moved endlessly between the photoreceptors 3Y, 3C, 3M, and 3K to form primary transfer nips. . Then, a transfer bias having a polarity opposite to that of the toner (for example, plus) is applied to the back surface (loop inner peripheral surface) of the intermediate transfer belt 14. The intermediate transfer belt 14 sequentially passes through the primary transfer nips for Y, C, M, and K along with the endless movement thereof, and on the front surface thereof, the intermediate transfer belt 14 is on the photoreceptors 3Y, 3C, 3M, and 3K. Y, C, M, and K toner images are superimposed and primarily transferred. As a result, a four-color superimposed toner image (hereinafter sometimes referred to as a four-color toner image) is formed on the intermediate transfer belt 14.

  The secondary transfer backup roller 66 sandwiches the intermediate transfer belt 14 with the secondary transfer roller 70 disposed outside the loop of the intermediate transfer belt 14 to form a secondary transfer nip. The registration roller pair 55 described above feeds the recording medium P sandwiched between the rollers toward the secondary transfer nip at a timing at which the recording medium P can be synchronized with the four-color toner image on the intermediate transfer belt 14. The four-color toner image on the intermediate transfer belt 14 is affected by the secondary transfer electric field formed between the secondary transfer roller 70 to which the secondary transfer bias is applied and the secondary transfer backup roller 66, and the influence of the nip pressure. Then, the secondary transfer is batch-transferred onto the recording medium P in the secondary transfer nip. Then, combined with the white color of the recording medium P, a full color toner image is obtained.

  Untransferred toner that has not been transferred to the recording medium P adheres to the intermediate transfer belt 14 after passing through the secondary transfer nip. This is cleaned by the belt cleaning unit 162. The belt cleaning unit 162 has a belt cleaning blade 162a in contact with the front surface of the intermediate transfer belt 14, thereby scraping off and removing the transfer residual toner on the intermediate transfer belt 14.

  The first bracket 63 of the transfer unit 60 swings at a predetermined rotation angle about the rotation axis of the auxiliary roller 68 as the solenoid (not shown) is turned on / off. When forming a monochrome image, the image forming apparatus 500 slightly rotates the first bracket 63 counterclockwise in FIG. 2 by driving the solenoid described above. By this rotation, the primary transfer rollers 7Y, 7C, and 7M for Y, C, and M are revolved counterclockwise in FIG. , M is separated from the photoconductors 3Y, 3C, 3M. Of the four image forming units 1Y, 1C, 1M, and 1K, only the K image forming unit 1K is driven to form a monochrome image. Accordingly, it is possible to avoid wear of each member constituting the image forming unit 1 due to wasteful driving of the Y, C, M image forming unit 1 during monochrome image formation.

  A fixing unit 80 is disposed above the secondary transfer nip in FIG. The fixing unit 80 includes a pressure heating roller 81 that contains a heat source such as a halogen lamp, and a fixing belt unit 82. The fixing belt unit 82 includes a fixing belt 84 as a fixing member, a heating roller 83 containing a heat source such as a halogen lamp, a tension roller 85, a driving roller 86, a temperature sensor (not shown), and the like. Then, the endless fixing belt 84 is endlessly moved in the counterclockwise direction in FIG. 2 while being stretched by the heating roller 83, the tension roller 85, and the driving roller 86. In the process of endless movement, the fixing belt 84 is heated from the back side by the heating roller 83. A pressurizing and heating roller 81 that is driven to rotate clockwise in FIG. 2 is in contact with the surface of the fixing belt 84 that is heated in this manner from the front surface side. Thus, a fixing nip where the pressure heating roller 81 and the fixing belt 84 abut is formed.

  A temperature sensor (not shown) is disposed outside the loop of the fixing belt 84 so as to face the front surface of the fixing belt 84 with a predetermined gap, and the fixing belt 84 just before entering the fixing nip. Detect surface temperature. This detection result is sent to a fixing power supply circuit (not shown). The fixing power supply circuit performs on / off control of power supply to the heat generation source included in the heating roller 83 and the heat generation source included in the pressure heating roller 81 based on the detection result of the temperature sensor.

  The recording medium P that has passed through the secondary transfer nip described above is separated from the intermediate transfer belt 14 and then sent into the fixing unit 80. Then, in the process of being conveyed from the lower side to the upper side in FIG. 2 while being sandwiched by the fixing nip in the fixing unit 80, the full-color toner image is fixed on the recording medium P by being heated and pressed by the fixing belt 84. Is done.

  The recording medium P on which the fixing process has been performed in this manner is discharged outside the apparatus after passing between the rollers of the discharge roller pair 87. A stack portion 88 is formed on the upper surface of the casing of the image forming apparatus 500 main body, and the recording media P discharged to the outside by the discharge roller pair 87 are sequentially stacked on the stack portion 88.

  Above the transfer unit 60, four toner cartridges 100Y, 100C, 100M, and 100K that store Y, C, M, and K toners are disposed. The Y, C, M, and K toners in the toner cartridges 100Y, 100C, 100M, and 100K are appropriately supplied to the developing devices 5Y, 5C, 5M, and 5K of the image forming units 1Y, 1C, 1M, and 1K. These toner cartridges 100Y, 100C, 100M, and 100K are detachable from the image forming apparatus main body independently of the image forming units 1Y, 1C, 1M, and 1K.

Next, an image forming operation in the image forming apparatus 500 will be described.
First, when a print execution signal is received from an operation unit (not shown) or the like, a predetermined voltage or current is sequentially applied to the charging roller 4 and the developing roller 51 at predetermined timings. Similarly, a predetermined voltage or current is sequentially applied to the optical writing unit 40 and a light source such as a static elimination lamp at a predetermined timing. In synchronism with this, the photosensitive member 3 is rotationally driven in the direction of the arrow in FIG. 2 by a photosensitive member driving motor (not shown) as driving means.

When the photoconductor 3 rotates in the direction of the arrow in FIG. 2, first, the surface of the photoconductor 3 is uniformly charged to a predetermined potential by the charging roller 4. Then, the laser beam L corresponding to the image information is irradiated onto the photoconductor 3 from the optical writing unit 40, and the portion irradiated with the laser light L on the surface of the photoconductor 3 is neutralized to form an electrostatic latent image. .
The surface of the photoreceptor 3 on which the electrostatic latent image is formed is rubbed by a developer magnetic brush formed on the developing roller 51 at a portion facing the developing device 5. At this time, the negatively charged toner on the developing roller 51 is moved to the electrostatic latent image side by a predetermined developing bias applied to the developing roller 51 to be converted into a toner image (development). In each image forming unit 1, the same image forming process is executed, and a toner image of each color is formed on the surface of each photoconductor 3Y, 3C, 3M, 3K of each image forming unit 1Y, 1C, 1M, 1K. .
As described above, in the image forming apparatus 500, the electrostatic latent image formed on the photoreceptor 3 is reversely developed by the developing device 5 with the negatively charged toner. In this embodiment, an example using a non-contact charging roller system of N / P (negative positive: toner adheres to a place where the potential is low) has been described, but the present invention is not limited to this.

The toner images of the respective colors formed on the surfaces of the photoreceptors 3Y, 3C, 3M, and 3K are sequentially primary-transferred so as to overlap on the surface of the intermediate transfer belt 14. As a result, a four-color toner image is formed on the intermediate transfer belt 14.
The four-color toner image formed on the intermediate transfer belt 14 is fed from the first paper feed cassette 151 or the second paper feed cassette 152, passed between the rollers of the registration roller pair 55, and fed to the secondary transfer nip. To the recording medium P to be transferred. At this time, the recording medium P is temporarily stopped while being sandwiched between the registration roller pair 55, and is supplied to the secondary transfer nip in synchronization with the leading edge of the image on the intermediate transfer belt 14. The recording medium P onto which the toner image has been transferred is separated from the intermediate transfer belt 14 and conveyed to the fixing unit 80. Then, the recording medium P to which the toner image is transferred passes through the fixing unit 80, whereby the toner image is fixed on the recording medium P by the action of heat and pressure, and the recording medium P on which the toner image is fixed is an image. It is discharged out of the forming apparatus 500 and stacked on the stack unit 88.

On the other hand, the transfer residual toner on the surface of the intermediate transfer belt 14 that has transferred the toner image onto the recording medium P at the secondary transfer nip is removed by the belt cleaning unit 162.
Further, the surface of the photoreceptor 3 on which the toner images of the respective colors are transferred to the intermediate transfer belt 14 at the primary transfer nip, the residual toner after the transfer is removed by the cleaning device 6, and the lubricant is applied by the lubricant applying device 10. Thereafter, the charge is removed by a charge removal lamp.

  As shown in FIG. 2, the image forming unit 1 of the image forming apparatus 500 includes a photoconductor 3 and a charging roller 4, a developing device 5, a cleaning device 6, a lubricant applying device 10, and the like as process means. It has been. The image forming unit 1 can be integrally attached to and detached from the main body of the image forming apparatus 500 as a process cartridge. In the image forming apparatus 500, the image forming unit 1 integrally replaces the photosensitive member 3 as a process cartridge and the process means, but the photosensitive member 3, the charging roller 4, the developing device 5, and the cleaning device 6. Alternatively, the lubricant application device 10 may be replaced with a new one in units. Further, the lubricant application device may not be used.

  As the toner used in the image forming apparatus 500, a polymerized toner manufactured by a suspension polymerization method, an emulsion polymerization method, or a dispersion polymerization method, which is easy to increase the circularity and reduce the particle size from the viewpoint of improving the image quality, is used. Is preferred. Among these, it is preferable to use a polymerized toner having a volume average particle size of 5.5 μm or less from the viewpoint of forming a high-resolution image.

  In the case of the high-circular and small particle size polymerized toner, the polymerized toner is sufficiently removed from the surface of the photoconductor 3 even if the cleaning blade 62 is used to remove the pulverized toner from the surface of the photoconductor 3 in the same manner as in the conventional case. Cannot be completely removed, resulting in poor cleaning. Therefore, when the contact pressure of the cleaning blade 62 to the photosensitive member 3 is increased to improve the cleaning performance, there is a problem that the cleaning blade 62 is worn out early. Further, the frictional force between the cleaning blade 62 and the photoconductor 3 is increased, and the contact portion (tip ridge line portion) 62c of the cleaning blade 62 that is in contact with the photoconductor 3 is pulled in the moving direction of the photoconductor 3, The contact portion 62c is bent (see FIGS. 7A to 7C). When the contact portion 62c of the cleaning blade 62 is rolled, various problems such as abnormal noise, vibration, and lack of the contact portion occur.

  As described above, the cleaning blade 62 of the present embodiment has been described with reference to FIG. 4A and 4B are enlarged sectional views of the cleaning blade 62 of FIG. 4A is an explanatory diagram of a state in which the cleaning blade 62 is in contact with the surface of the photoreceptor 3, and FIG. 4B is a diagram in the vicinity of the tip ridge line portion (contact portion) 62c of the cleaning blade 62. FIG. Hereinafter, description will be made using the image carrier 3 as a member to be cleaned and toner as a deposit.

As shown in FIG. 1, the cleaning blade 62 includes a flat support member 621 made of a rigid material such as metal or hard plastic, and a strip-shaped elastic member 622. The elastic member 622 is fixed to one end side of the support member 621 by an adhesive or the like, and the other end side of the support member 621 is cantilevered by the case of the cleaning device 6.
As shown in FIG. 4A, the cleaning blade 62 includes a support member 621 and a strip-shaped elastic member 622 having one end connected to the support member and the other end having a free end of a predetermined length. . A tip ridge line portion 62c, which is one end on the free end side of the elastic member 622, is disposed so as to contact the surface of the photosensitive member (image carrier) 3 along the longitudinal direction.

  The elastic member 622 preferably has a high resilience rate so that it can follow the eccentricity of the photosensitive member 3 and minute undulations on the surface of the photosensitive member 3, and a polyurethane rubber or the like is preferable. The elastic member preferably has a JIS-A hardness of 60 degrees or more. Moreover, the rebound resilience rate based on the JIS K6255 standard of the elastic member is 36% to 72% at 23 ° C.

The tip ridge line portion (contact portion) 62c that contacts the surface of the image carrier of the elastic member 622 has a (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule (particularly, a tricyclodecane structure). A cured product of an ultraviolet curable composition containing a (meth) acrylate compound or a (meth) acrylate compound having an adamantane structure is preferred.
After impregnating the contact portion of the elastic member with an ultraviolet curable composition containing a (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule, irradiation with ultraviolet rays results in FIG. ) Is formed, the hardness of the tip ridge line portion (contact portion) 62c is increased, the durability is improved, and the elastic member is deformed in the direction of movement of the image carrier 3 surface. Can be suppressed. Furthermore, even when the inside is exposed due to wear of the surface layer over time, the modification layer 62d can similarly suppress deformation.

(Process cartridge)
The process cartridge of the present invention comprises at least an image carrier and cleaning means for removing toner remaining on the image carrier, and further comprises other means as necessary.
As the cleaning means, the cleaning blade of the present invention is used.
The process cartridge includes an image carrier and the cleaning blade of the present invention, and further includes at least one of a charging unit, an exposure unit, a developing unit, a transfer unit, a cleaning unit, and a charge eliminating unit. An apparatus (part) that is detachable from the image forming apparatus.

  Examples of the present invention will be described below, but the present invention is not limited to these examples.

<JIS-A hardness of elastic member>
The JIS-A hardness of the elastic member was measured according to JIS K6253 using a micro rubber hardness meter MD-1 manufactured by Kobunshi Keiki Co., Ltd. In addition, about the elastic member of 2 layer structure, it measured from each surface side.

<Rebound resilience of elastic member>
The rebound resilience of the elastic member is No. manufactured by Toyo Seiki Seisakusho Co., Ltd. The measurement was performed according to JIS K6255 using a 221 regilynester. The measurement sample was obtained by superposing sheets having a thickness of about 2 mm so that the thickness was 4 mm or more. At the time of measurement, the part other than the reforming part was measured.

<Average circularity of toner>
The average circularity of the toner was measured by a flow type particle image analyzer (FPIA-2000, manufactured by Sysmex Corporation). Specifically, 0.1 mL to 0.5 mL of a surfactant (alkylbenzene sulfonate) is added as a dispersant to 100 mL to 150 mL of water from which impure solids have been removed in advance, and a measurement sample (toner) About 0.1 to 0.5 g was added. Thereafter, the suspension in which the toner is dispersed is subjected to a dispersion treatment with an ultrasonic disperser for 1 to 3 minutes so that the concentration of the dispersion becomes 3,000 / μL to 10,000 / μL. Was set in the analyzer, and the shape and distribution of the toner were measured. Based on the measurement result, the outer peripheral length of the actual toner projection shape shown in FIG. 5A is C1, and the projection area is S. The outer circumference of the perfect circle shown in FIG. C2 / C1 was determined when the length was C2, and the average value was defined as the average circularity.

<Volume average particle diameter of toner>
The volume average particle diameter of the toner was determined by a Coulter counter method. Specifically, toner number distribution and volume distribution data measured by a Coulter Multisizer 2e type (manufactured by Beckman Coulter) were sent to a personal computer via an interface (manufactured by Nikkiki Co., Ltd.) for analysis. More specifically, a 1% by mass NaCl aqueous solution using primary sodium chloride was prepared as an electrolytic solution. Then, 0.1 mL to 5 mL of a surfactant (alkyl benzene sulfonate) was added as a dispersant to 100 mL to 150 mL of the electrolytic aqueous solution. Further, 2 mg to 20 mg of toner as a test sample was added thereto, and dispersed with an ultrasonic disperser for 1 minute to 3 minutes. Then, 100 mL to 200 mL of the electrolytic aqueous solution was put into another beaker, and the solution after the dispersion treatment was added therein to a predetermined concentration, and applied to the Coulter Multisizer 2e type.
The aperture is 100 μm, and the particle size of 50,000 toner particles is measured. As a channel, it is 2.00 micrometers or more and less than 2.52 micrometers; 2.52 micrometers or more and less than 3.17 micrometers; 3.17 micrometers or more and less than 4.00 micrometers; 4.00 micrometers or more and less than 5.04 micrometers; 5.04 micrometers or more and less than 6.35 micrometers; .35 μm or more and less than 8.00 μm; 8.00 μm or more and less than 10.08 μm; 10.08 μm or more and less than 12.70 μm; 12.70 μm or more and less than 16.00 μm; 16.00 μm or more and less than 20.20 μm; Less than 40 μm; 25.40 μm or more and less than 32.00 μm; 13 channels of 32.00 μm or more and less than 40.30 μm were used, and toner particles having a particle size of 2.00 μm or more and 32.0 μm or less were targeted.
The volume average particle diameter was calculated based on the relational expression “volume average particle diameter = ΣXfV / ΣfV”. However, “X” is the representative diameter in each channel, “V” is the equivalent volume in the representative diameter of each channel, and “f” is the number of particles in each channel.

Next, a verification experiment conducted by the applicants will be described.
The verification experiment shown below was performed by changing the physical properties of the elastic member 622 and the impregnation treatment material (effect material) of the modified layer 62d.
(Production Example 1)
-Production of elastic members 1-5-
As the elastic member, five polyurethane rubbers having the following physical properties at 23 [° C.] were prepared. Each of the five polyurethane rubbers has a flat plate shape with an average thickness of 1.8 mm, 11.5 mm × 32.6 mm.
Elastic member 1: hardness 76 degrees, rebound resilience 36 [%] (manufactured by Toyo Tire & Rubber Co., Ltd.)
-Elastic member 2: hardness 70 degrees, rebound resilience 52 [%] (manufactured by Toyo Tire & Rubber Co., Ltd.)
Elastic member 3: hardness 78 degrees, rebound resilience 54 [%] (manufactured by Toyo Tire & Rubber Co., Ltd.)
Elastic member 4: hardness 63 degrees, rebound resilience 72 [%] (manufactured by Toyo Tire & Rubber Co., Ltd.)
-Elastic member 5: hardness 68 degrees, rebound resilience 30 [%] (manufactured by Toyo Tire & Rubber Co., Ltd.)

・重合開始剤（チバ・スペシャリティーケミカルズ社製、イルガキュア１８４）・・・５質量部
・溶媒（シクロヘキサノン）・・・５５質量部 (Preparation Example 1)
-Preparation of UV curable composition 1-
From the following composition, an ultraviolet curable composition 1 was prepared by a conventional method.
Tricyclodecane dimethanol diacrylate represented by the following structural formula (manufactured by Shin-Nakamura Chemical Co., Ltd., trade name: A-DCP, functional group number 2, molecular weight 304): 50 parts by mass

・ Polymerization initiator (Ciba Specialty Chemicals, Irgacure 184) ・ ・ ・ 5 parts by mass ・ Solvent (cyclohexanone) ... 55 parts by mass

ただし、式中、Ｒは水素原子、又はメチル基を表す。
・重合開始剤（チバ・スペシャリティーケミカルズ社製、イルガキュア１８４）・・・５質量部
・溶媒（シクロヘキサノン）・・・５５質量部 (Preparation Example 2)
-Preparation of UV curable composition 2-
From the following composition, an ultraviolet curable composition 2 was prepared by a conventional method.
-(Meth) acrylate compound 1 having an adamantane structure represented by the following structural formula (Idemitsu Kosan Co., Ltd., X-DA, functional group number 2, molecular weight 276 to 304, reaction of 1,3-adamantanediol with acrylic acid Product) ... 50 parts by mass

However, in the formula, R represents a hydrogen atom or a methyl group.
・ Polymerization initiator (Ciba Specialty Chemicals, Irgacure 184) ・ ・ ・ 5 parts by mass ・ Solvent (cyclohexanone) ... 55 parts by mass

・重合開始剤（チバ・スペシャリティーケミカルズ社製、イルガキュア１８４）・・・
５質量部
・溶媒（シクロヘキサノン）・・・５５質量部 (Preparation Example 3)
-Preparation of UV curable composition 3-
From the following composition, an ultraviolet curable composition 3 was prepared by a conventional method.
(Meth) acrylate compound 2 having an adamantane structure represented by the following structural formula (1,3-adamantane dimethanol diacrylate, manufactured by Idemitsu Kosan Co., Ltd., X-A-201, functional group number 2, molecular weight 304)・ 50 parts by mass

・ Polymerization initiator (Irgacure 184, manufactured by Ciba Specialty Chemicals)
5 parts by mass-Solvent (cyclohexanone) 55 parts by mass

・重合開始剤（チバ・スペシャリティーケミカルズ社製、イルガキュア１８４）・・・５質量部
・溶媒（シクロヘキサノン）・・・５５質量部 (Preparation Example 4)
-Preparation of UV curable composition 4-
From the following composition, an ultraviolet curable composition 4 was prepared by a conventional method.
-(Meth) acrylate compound 3 having an adamantane structure represented by the following structural formula (Mitsubishi Gas Chemical Co., Ltd., Dia Purest ADTM, functional group number 3, molecular weight 388): 50 parts by mass

・ Polymerization initiator (Ciba Specialty Chemicals, Irgacure 184) ・ ・ ・ 5 parts by mass ・ Solvent (cyclohexanone) ... 55 parts by mass

・重合開始剤（チバ・スペシャリティーケミカルズ社製、イルガキュア１８４）・・・５質量部
・溶媒（シクロヘキサノン）・・・５５質量部 (Preparation Example 5)
-Preparation of UV curable composition 5-
From the following composition, an ultraviolet curable composition 5 was prepared by a conventional method.
-Tricyclodecane dimethanol diacrylate represented by the above structural formula (manufactured by Shin-Nakamura Chemical Co., Ltd., A-DCP, functional group number 2, molecular weight 304) ... 25 parts by mass-Penta represented by the following structural formula Erythritol triacrylate (Daicel Cytec, PETIA, functional group number 3, molecular weight 298): 25 parts by mass

・ Polymerization initiator (Ciba Specialty Chemicals, Irgacure 184) ・ ・ ・ 5 parts by mass ・ Solvent (cyclohexanone) ... 55 parts by mass

(Preparation Example 6)
-Preparation of UV curable composition 6-
From the following composition, an ultraviolet curable composition 6 was prepared by a conventional method.
(Meth) acrylate compound 2 having an adamantane structure represented by the above structural formula (1,3-adamantane dimethanol diacrylate, manufactured by Idemitsu Kosan Co., Ltd., X-A-201, functional group number 2, molecular weight 304) 25 parts by mass Pentaerythritol triacrylate represented by the above structural formula (Daicel Cytec, PETIA, functional group number 3, molecular weight 298) ... 25 parts by mass Polymerization initiator (Ciba Specialty Chemicals, Irgacure 184) ... 5 parts by mass Solvent (cyclohexanone) ... 55 parts by mass

(Preparation Example 7)
-Preparation of UV curable composition 7-
From the following composition, an ultraviolet curable composition 7 was prepared by a conventional method.
Pentaerythritol triacrylate represented by the above structural formula (Daicel Cytec, PETIA, functional group number 3, molecular weight 298): 50 parts by mass Polymerization initiator (Ciba Specialty Chemicals, Irgacure 184)・ ・ 5 parts by mass ・ Solvent (cyclohexanone): 55 parts by mass

・重合開始剤（チバ・スペシャリティーケミカルズ社製、イルガキュア１８４）・・・５質量部
・溶媒（シクロヘキサノン）・・・５５質量部 (Preparation Example 8)
-Preparation of UV curable composition 8-
From the following composition, an ultraviolet curable composition 8 was prepared by a conventional method.
Dipentaerythritol hexaacrylate represented by the following structural formula (manufactured by Daicel Cytec, DPHA, functional group number 6, molecular weight 578) ... 59 parts by mass

・ Polymerization initiator (Ciba Specialty Chemicals, Irgacure 184) ・ ・ ・ 5 parts by mass ・ Solvent (cyclohexanone) ... 55 parts by mass

・重合開始剤（チバ・スペシャリティーケミカルズ社製、イルガキュア１８４）・・・５質量部
・溶媒（シクロヘキサノン）・・・５５質量部 (Preparation Example 9)
-Preparation of UV curable composition 9-
From the following composition, an ultraviolet curable composition 9 was prepared by a conventional method.
-Ethoxylated bisphenol A diacrylate represented by the following structural formula (manufactured by Shin-Nakamura Chemical Co., ABE-300, functional group number 2, molecular weight 466): 50 parts by mass

・ Polymerization initiator (Ciba Specialty Chemicals, Irgacure 184) ・ ・ ・ 5 parts by mass ・ Solvent (cyclohexanone) ... 55 parts by mass

<Example of toner production>
Toner base particles having an average circularity of 0.98 and a volume average particle size of 4.9 μm were prepared by a polymerization method. With respect to 100 parts by mass of the obtained toner base particles, 1.5 parts by mass of silica fine particles having a small particle size (manufactured by Clariant Co., Ltd., H2000), titanium oxide fine particles having a small particle size (manufactured by Teika Co., Ltd., MT-150AI) 0 A toner was prepared by stirring and mixing 5 parts by mass of silica particles having a large particle diameter (manufactured by Denki Kagaku Kogyo Co., Ltd., UFP-30H) with a Henschel mixer.

Example 1
<Preparation of cleaning blade 1>
In a liquid diluted with a diluent (cyclohexanone) so that the solid content concentration of the ultraviolet curable composition 1 is 50% by mass, a portion 2 mm from the tip of the elastic member 1 on the side in contact with the image carrier is placed. After soaking for 2 hours, it was air-dried for 3 minutes. After air drying, ultraviolet irradiation (140 W / cm × 5 m / min × 5 passes) was performed using an ultraviolet irradiation device (manufactured by USHIO INC., UVC-2534 / 1MNLC3). Next, drying was performed for 15 minutes at an internal temperature of 100 ° C. using a heat dryer.
Next, the elastic member 1 after the surface curing treatment was fixed to a sheet metal holder as a support member with an adhesive, and the cleaning blade 1 was produced.

Next, the produced cleaning blade 1 was attached to a color multifunction machine (image MPC5001, manufactured by Ricoh Co., Ltd.) with a predetermined tip biting amount (linear pressure) and attachment angle. The linear pressure and the mounting angle differ depending on the cleaning blade sample type.
Also, the lubricant application device was removed.
A chart with an image area ratio of 20% (A4 size horizontal), in which the toner is mounted on the color multifunction peripheral (image MPC5001, manufactured by Ricoh Co., Ltd.) and a vertical belt portion is provided in an environment of 55% RH at 23 ° C. After printing 10,000 sheets at 3 prints / job, the contact state observation, the cleaning property, and the wear amount of the contact portion were evaluated as follows. The results are shown in Table 1.

<A contact state observation>
The contact state of the cleaning blade when the cleaning blade is rubbed with the predetermined edge biting amount (linear pressure) and the mounting angle on the glass plate coated with the material used for the surface layer of the photoreceptor. The length of the contact portion of the elastic member of the cleaning blade was observed using the image output from the CCD camera (Nikon CM-5, manufactured by Nikon Corporation).

<Cleanability>
After the output of 10,000 sheets, the vertical band pattern (with respect to the paper traveling direction) is 43 mm wide, and the output image after 20 images at the time of evaluation of 3 charts (A4 size landscape) are visually observed. The cleaning properties were evaluated according to the following criteria. Note that an abnormal image means an image or white spot image that appears in a streak or strip shape in a printed image.
〔Evaluation criteria〕
○: No abnormal image ×: There is an abnormal image

<Abrasion amount of contact part>
After the output of 10,000 sheets, the amount of wear at the contact portion of the elastic member, as shown in FIG. Measured by 9510.

(Examples 2 to 10 and Comparative Examples 1 to 4)
In Example 1, cleaning blades of Examples 2 to 10 and Comparative Examples 1 to 4 were prepared in the same manner as Example 1 except that the elastic member and the ultraviolet curable composition shown in Table 1 were used. .
For each of the obtained cleaning blades, the contact state between the cleaning blade and the photosensitive member, the cleaning property, and the wear amount of the contact portion were evaluated in the same manner as in Example 1. The results are shown in Table 1.

Table 1 shows the results of the verification experiments of the examples and comparative examples.

From the result of Table 1, since the comparative example 1 does not have the modified layer by the ultraviolet curable resin in the front-end | tip ridgeline part 62c of the elastic member 622, generation | occurrence | production of the front-end | tip ridgeline part 62c or the front-end | tip ridgeline part by this wrinkle A vibration of 62c was generated. As a result, good cleaning performance on the surface of the member to be cleaned could not be maintained, and white spots due to deposits on the surface of the member to be cleaned occurred in the printed image.
Further, in Comparative Example 2, the elastic member has a rebound resilience of 36% or less, so the flexibility of the entire elastic member is lost, and it becomes impossible to follow the vibration of the member to be cleaned and the roughness of the surface of the member to be cleaned. A defect occurred and some vertical streaks occurred in the printed image.

  Moreover, the comparative example 3 and the comparative example 4 contain the (meth) acrylate compound which has a C6 or more alicyclic structure in a molecule | numerator in the modified layer by the ultraviolet curable resin of the front-end | tip ridgeline part 62c of the elastic member 622. It does not contain a cured product of the ultraviolet curable composition. For this reason, the leading edge ridge line portion of the elastic member is bent due to friction over time, and vertical stripes are generated in the printed image.

On the other hand, in Examples 1-10, the hardened | cured material of the ultraviolet curable composition containing the (meth) acrylate compound which has a C6 or more alicyclic structure in a molecule | numerator in the front-end ridgeline part 62c of the elastic member 622 is used. The rebound resilience of the elastic member 622 other than the reforming layer 62d is 36% or more and 72% or less at 23 ° C. For this reason, the edge ridge line part 62c of which the hardness of the elastic member 622 is increased can maintain the flexibility that can follow the shake and surface roughness of the photoreceptor, and the tip of the elastic member can be compared with Comparative Examples 1 to 4. The ridgeline portion was prevented from curling and wearing, and good cleaning properties could be maintained over a long period of time.
In Example 10, although slight crease occurred in the tip ridge line portion 62c of the elastic member 622, the cleaning property could be maintained by the elasticity of the elastic member 622.

  Moreover, in Examples 1-9, the molecular weight of the (meth) acrylate compound which has a C6 or more alicyclic structure in the said molecule | numerator is 450 or less. For this reason, it becomes easy to impregnate the elastic member with a (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule, and compared with Example 10 in which the molecular weight exceeds 450, the tip ridge portion 62c It was possible to increase the hardness and suppress the amount of wear.

What has been described above is merely an example, and the present invention has a specific effect for each of the following modes.
(Aspect A)
A toner which is made of an elastic member such as a strip-shaped elastic member 622 and contacts the surface of the member to be cleaned such as the photosensitive member 3 moving on the front end ridge line portion 62c of the elastic member and adheres to the surface of the member to be cleaned. In a cleaning blade such as the cleaning blade 62 that removes deposits such as the above, the contact portion 62c of the elastic member with the surface of the member to be cleaned has an alicyclic structure having 6 or more carbon atoms in the molecule (meta). It has a modified layer such as a modified layer 62d containing a cured product of an ultraviolet curable composition containing an acrylate compound, and the resilience elastic modulus at a portion other than the modified layer of the elastic member is 36% or more 72% at 23 ° C. % Or less.

In this embodiment, the tip ridge line portion (contact portion) 62c of the elastic member 622 includes a cured product of an ultraviolet curable composition containing a (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule. It has a modified layer 62d. Thereby, the tip ridge line part (contact part) 62c of the elastic member 622 is increased in hardness, and the contact part can be prevented from being bent or deformed.
In this embodiment, the resilience modulus at a portion other than the modified layer 62d of the elastic member 622 is not less than 36% and not more than 72% at 23 ° C. As a result, as shown in the verification experiment, the elastic member can maintain the flexibility that can follow the shake and surface roughness of the photosensitive member, and in the cleaning blade in which the contact portion with the member to be cleaned has a high hardness. Further, it is possible to prevent the tip ridge line portion of the elastic member from being curled and worn, and to maintain good cleaning properties for a long period of time.

(Aspect B)
In Aspect A, the number of functional groups of the (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule is 2 to 6. According to this, as described in the above embodiment, when the number of functional groups is less than 2, the hardness of the contact portion may be weak, and when it exceeds 6, steric hindrance may occur.

(Aspect C)
In the aspect A or the aspect B, the molecular weight of the (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule is 450 or less. According to this, as described in the above embodiment, when the molecular weight exceeds 500, the molecular size increases, so that it is difficult to impregnate the elastic member, and high hardness may be difficult.

(Aspect D)
In any of Aspects A to C, the (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule, a (meth) acrylate compound having a tricyclodecane structure, and a (meth) acrylate having an adamantane structure It is at least one selected from compounds. According to this, as described in the above embodiment, the lack of crosslinking points can be compensated for by a special cyclic structure even if there are few functional groups.

(Aspect E)
In aspect D, the (meth) acrylate compound having a tricyclodecane structure is at least one selected from tricyclodecane dimethanol diacrylate and tricyclodecane dimethanol dimethacrylate.

(Aspect F)
In aspect D, the (meth) acrylate compound having an adamantane structure is 1,3-adamantane dimethanol diacrylate, 1,3-adamantane dimethanol dimethacrylate, 1,3,5-adamantane trimethanol triacrylate, and 1 , 3,5-adamantane trimethanol trimethacrylate.

(Aspect G)
In any of Embodiments A to F, the ultraviolet curable composition further contains a (meth) acrylate compound having a pentaerythritol tri (meth) acrylate structure having 3 to 6 functional groups.

(Aspect H)
An image carrier, a charging unit for charging the surface of the image carrier, an exposure unit for exposing the charged image carrier to form an electrostatic latent image, and developing the electrostatic latent image using toner Developing means for forming a visible image, transfer means for transferring the visible image to a recording medium, fixing means for fixing the transferred image transferred to the recording medium, and remaining on the image carrier. An image forming apparatus having a cleaning unit that removes toner, wherein the cleaning blade according to any one of aspects A to F is used as the cleaning unit.
With such a configuration, it is possible to maintain good cleaning properties and obtain a good image.

(Aspect I)
8. A process cartridge comprising at least an image carrier and a cleaning unit for removing toner remaining on the image carrier, wherein the cleaning blade according to claim 1 is used as the cleaning unit. According to this, as described in the above embodiment, a good cleaning property can be obtained. In addition, operability can be improved by taking the form of a process cartridge.

DESCRIPTION OF SYMBOLS 1 Image forming unit 3 Photoconductor 4 Charging roller 5 Developing device 6 Cleaning device 14 Intermediate transfer belt 60 Transfer unit 62 Cleaning blade 62c Tip edge part 62d Modified layer 80 Fixing unit 100 Toner cartridge 500 Image forming device 621 Support member 622 Elastic member

Japanese Patent No. 3602898 JP 2004-233818 A JP 2010-152295 A

Claims (8)

In a cleaning blade that consists of a strip-shaped elastic member, abuts against the surface of the member to be cleaned that moves the tip ridge line portion of the elastic member, and removes adhering matter attached to the surface of the member to be cleaned.
Modification in which the contact portion of the elastic member with the surface of the member to be cleaned contains a cured product of an ultraviolet curable composition containing a (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule a layer state, and it is impact resilience less 72% 36% or more at 23 ° C. in a portion other than the modified layer of the elastic member,
The (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule is at least one selected from a (meth) acrylate compound having a tricyclodecane structure and a (meth) acrylate compound having an adamantane structure The cleaning blade characterized by being. The cleaning blade of claim 1.
The cleaning blade, wherein the number of functional groups of the (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule is 2 to 6. The cleaning blade according to claim 1 or 2,
A cleaning blade, wherein the molecular weight of a (meth) acrylate compound having an alicyclic structure having 6 or more carbon atoms in the molecule is 450 or less . In the cleaning blade of 請 Motomeko 1,
The cleaning blade according to claim 1, wherein the (meth) acrylate compound having a tricyclodecane structure is at least one selected from tricyclodecane dimethanol diacrylate and tricyclodecane dimethanol dimethacrylate. The cleaning blade of claim 1 .
The (meth) acrylate compound having an adamantane structure includes 1,3-adamantane dimethanol diacrylate, 1,3-adamantane dimethanol dimethacrylate, 1,3,5-adamantane trimethanol triacrylate, and 1,3,5. -A cleaning blade, which is at least one selected from adamantanetrimethanol trimethacrylate. The cleaning blade according to any one of claims 1 to 5 ,
The cleaning blade, wherein the ultraviolet curable composition further contains a (meth) acrylate compound having a pentaerythritol tri (meth) acrylate structure having 3 to 6 functional groups. An image carrier, a charging unit for charging the surface of the image carrier, an exposure unit for exposing the charged image carrier to form an electrostatic latent image, and developing the electrostatic latent image using toner Developing means for forming a visible image, transfer means for transferring the visible image to a recording medium, fixing means for fixing the transferred image transferred to the recording medium, and remaining on the image carrier. an image forming apparatus having a cleaning means for removing the toner, an image forming apparatus, wherein the cleaning means is any one of a cleaning blade according to claim 1 to 6. A process cartridge having at least an image carrier and a cleaning unit for removing toner remaining on the image carrier, wherein the cleaning unit is the cleaning blade according to any one of claims 1 to 6. Feature process cartridge.

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