JP2003043817A - Electrophotographic device and process cartridge - Google Patents
Electrophotographic device and process cartridgeInfo
- Publication number
- JP2003043817A JP2003043817A JP2001229902A JP2001229902A JP2003043817A JP 2003043817 A JP2003043817 A JP 2003043817A JP 2001229902 A JP2001229902 A JP 2001229902A JP 2001229902 A JP2001229902 A JP 2001229902A JP 2003043817 A JP2003043817 A JP 2003043817A
- Authority
- JP
- Japan
- Prior art keywords
- developer
- photosensitive member
- charging
- electrophotographic photosensitive
- electrophotographic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
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- 238000012546 transfer Methods 0.000 claims abstract description 35
- 239000000463 material Substances 0.000 claims abstract description 26
- 108091008695 photoreceptors Proteins 0.000 claims abstract description 13
- 239000002344 surface layer Substances 0.000 claims abstract description 8
- 238000011144 upstream manufacturing Methods 0.000 claims abstract description 5
- 229920001230 polyarylate Polymers 0.000 claims description 21
- 239000000126 substance Substances 0.000 claims description 10
- 239000004431 polycarbonate resin Substances 0.000 claims description 7
- 229920005668 polycarbonate resin Polymers 0.000 claims description 7
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- 239000002904 solvent Substances 0.000 description 6
- 238000004140 cleaning Methods 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
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- 229920000297 Rayon Polymers 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
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- 229910052751 metal Inorganic materials 0.000 description 2
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- 150000002739 metals Chemical class 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920005990 polystyrene resin Polymers 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- LHENQXAPVKABON-UHFFFAOYSA-N 1-methoxypropan-1-ol Chemical compound CCC(O)OC LHENQXAPVKABON-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 101100321670 Fagopyrum esculentum FA18 gene Proteins 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 229910006404 SnO 2 Inorganic materials 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- ZTWQZJLUUZHJGS-UHFFFAOYSA-N Vat Yellow 4 Chemical compound C12=CC=CC=C2C(=O)C2=CC=C3C4=CC=CC=C4C(=O)C4=C3C2=C1C=C4 ZTWQZJLUUZHJGS-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- PGEHNUUBUQTUJB-UHFFFAOYSA-N anthanthrone Chemical compound C1=CC=C2C(=O)C3=CC=C4C=CC=C5C(=O)C6=CC=C1C2=C6C3=C54 PGEHNUUBUQTUJB-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
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- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- NKDDWNXOKDWJAK-UHFFFAOYSA-N dimethoxymethane Chemical compound COCOC NKDDWNXOKDWJAK-UHFFFAOYSA-N 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- -1 hydrazone compounds Chemical class 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002916 oxazoles Chemical class 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- 150000003219 pyrazolines Chemical class 0.000 description 1
- WVIICGIFSIBFOG-UHFFFAOYSA-N pyrylium Chemical compound C1=CC=[O+]C=C1 WVIICGIFSIBFOG-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 229920000638 styrene acrylonitrile Polymers 0.000 description 1
- 229920003066 styrene-(meth)acrylic acid ester copolymer Polymers 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 125000005259 triarylamine group Chemical group 0.000 description 1
- 238000001132 ultrasonic dispersion Methods 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
Landscapes
- Photoreceptors In Electrophotography (AREA)
- Dry Development In Electrophotography (AREA)
- Cleaning In Electrography (AREA)
- Electrostatic Charge, Transfer And Separation In Electrography (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、電子写真装置及び
プロセスカートリッジに関し、詳しくは、クリーナー手
段を必要としない電子写真装置及びプロセスカートリッ
ジに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrophotographic apparatus and a process cartridge, and more particularly to an electrophotographic apparatus and a process cartridge that do not require a cleaner.
【0002】[0002]
【従来の技術】従来、複写機あるいはプリンタやファク
シミリ等の電子写真方式を用いた電子写真装置は、潜像
担持体である電子写真感光体、その電子写真感光体を帯
電処理する帯電装置、電子写真感光体上に形成された静
電潜像を現像剤であるトナーにより顕像化する現像装
置、紙等の転写材に上記トナーを転写する転写装置、そ
の後の電子写真感光体上に残された残留トナーをクリー
ニングするクリーニング装置、転写材上のトナーを定着
させる定着装置等から構成されている。2. Description of the Related Art Conventionally, an electrophotographic apparatus using an electrophotographic system such as a copying machine, a printer or a facsimile is an electrophotographic photosensitive member which is a latent image carrier, a charging device for charging the electrophotographic photosensitive member, and an electronic device. A developing device that visualizes the electrostatic latent image formed on the photographic photoconductor with toner that is a developer, a transfer device that transfers the toner to a transfer material such as paper, and then remains on the electrophotographic photoconductor. It comprises a cleaning device for cleaning the residual toner, a fixing device for fixing the toner on the transfer material, and the like.
【0003】近年、環境保全や資源の有効利用の点か
ら、クリーニング装置にて回収されている転写残トナー
いわゆる廃トナーを現像装置に戻し再利用する電子写真
装置が開発されている。この一つの方式に、クリーニン
グ装置を廃し、転写残トナーの清掃は現像装置において
現像行程と同時に行うというクリーナーレス方式という
ものがある。In recent years, from the viewpoint of environmental protection and effective use of resources, an electrophotographic apparatus has been developed in which transfer residual toner, so-called waste toner, collected by a cleaning device is returned to a developing device for reuse. As one of the methods, there is a cleanerless method in which the cleaning device is eliminated and the transfer residual toner is cleaned in the developing device at the same time as the developing process.
【0004】転写後の電子写真感光体に残存する転写残
トナーは、クリーニング装置によって電子写真感光体面
から除去されて廃トナーとなるが、クリーナーを無く
し、転写後の電子写真感光体上の転写残トナーは現像装
置によって電子写真感光体上から除去し、現像装置に回
収・再使用する装置構成にしたクリーナーレスプロセス
の電子写真装置等が提案されている。例えば、特開平8
−137368号公報に示されているのは、帯電手段で
ある帯電ローラーの上流側に帯電手段と同極性でしかも
より高い電位に転写残トナーを帯電させる補助帯電手段
を設けて帯電ローラーへの転写残トナー付着による汚れ
を防止すると同時に、帯電ローラーにAC電圧を重畳す
ることで均一な帯電を行うと同時に転写残トナーの除電
を行い現像装置での回収を行うというものである。The transfer residual toner remaining on the electrophotographic photosensitive member after the transfer is removed from the surface of the electrophotographic photosensitive member by a cleaning device to become waste toner, but the cleaner is eliminated and the transfer residual toner on the electrophotographic photosensitive member after the transfer is removed. There is proposed a cleanerless process electrophotographic apparatus in which toner is removed from the electrophotographic photosensitive member by a developing apparatus and is collected and reused in the developing apparatus. For example, JP-A-8
Japanese Patent Laid-Open No. 137368 discloses that an auxiliary charging unit for charging transfer residual toner to the charging roller, which has the same polarity as the charging unit and has a higher potential, is provided on the upstream side of the charging roller which is the charging unit. While preventing the stain due to the adhesion of the residual toner, the AC voltage is superposed on the charging roller to perform uniform charging, and at the same time, the residual transfer toner is discharged to be collected by the developing device.
【0005】[0005]
【発明が解決しようとする課題】しかしながらこのプロ
セスは、帯電ローラーに重畳するAC電圧が高いとその
振動電界により電子写真感光体表面が粗らされ、帯電ロ
ーラーと電子写真感光体のニップ部を転写残トナーが通
過する際、電子写真感光体表面に付着、いわゆるトナー
融着の現象が発生し、画像欠陥を起こしてしまう。一
方、AC電圧が低い場合には、転写残トナーの除電が上
手く行われないために現像装置での回収が難しくなりか
ぶり画像を発生させてしまう。すなわち、重畳するAC
電圧を正確に制御しなければこの2つの問題を両立させ
ることが難しい訳である。However, in this process, when the AC voltage superimposed on the charging roller is high, the surface of the electrophotographic photosensitive member is roughened by the oscillating electric field, and the nip portion between the charging roller and the electrophotographic photosensitive member is transferred. When the residual toner passes through, a phenomenon of adhesion, that is, toner fusion, occurs on the surface of the electrophotographic photosensitive member, causing an image defect. On the other hand, when the AC voltage is low, the charge of the transfer residual toner is not properly removed, so that it is difficult to collect in the developing device and a fog image is generated. That is, the superposed AC
Unless the voltage is accurately controlled, it is difficult to make these two problems compatible.
【0006】本発明の目的は、トナー融着とかぶりの問
題を両立できるクリーナーレスシステムの電子写真装置
及びプロセスカートリッジを提供することにある。An object of the present invention is to provide an electrophotographic apparatus and a process cartridge of a cleanerless system which can solve the problems of toner fusion and fogging.
【0007】[0007]
【課題を解決するための手段】本発明に従って、電子写
真感光体と、電子写真感光体を帯電する帯電手段と、帯
電処理された電子写真感光体に静電潜像を形成する情報
書き込み手段と、静電潜像に現像剤を供給し静電潜像を
可視化する現像手段と、可視化した現像剤像を転写材に
転写する転写手段と、該帯電手段より上流に位置してい
て、電子写真感光体面上の現像剤を帯電する現像剤帯電
量制御手段とを有し、転写工程後の電子写真感光体上に
残余する現像剤を、該現像剤帯電量制御手段で正規極性
に帯電処理し、該帯電手段で該電子写真感光体面を帯電
すると同時に、適正帯電量にする電子写真装置におい
て、該電子写真感光体が表面層にポリアリレート樹脂を
含有することを特徴とする電子写真装置及びプロセスカ
ートリッジが提供される。According to the present invention, an electrophotographic photosensitive member, a charging means for charging the electrophotographic photosensitive member, and an information writing means for forming an electrostatic latent image on the charged electrophotographic photosensitive member. A developing unit for supplying a developer to the electrostatic latent image to visualize the electrostatic latent image; a transferring unit for transferring the visualized developer image to a transfer material; and an electrophotographic apparatus located upstream of the charging unit. A developer charge amount control means for charging the developer on the surface of the photoconductor is provided, and the developer remaining on the electrophotographic photoconductor after the transfer step is charged to a normal polarity by the developer charge amount control means. An electrophotographic apparatus for charging the surface of the electrophotographic photosensitive member by the charging unit and at the same time providing an appropriate amount of charge, wherein the electrophotographic photosensitive member contains a polyarylate resin in a surface layer Cartridge provided That.
【0008】[0008]
【発明の実施の形態】以下に、本発明の実施の形態を詳
細に説明する。BEST MODE FOR CARRYING OUT THE INVENTION Embodiments of the present invention will be described in detail below.
【0009】本発明に係る電子写真感光体が表面層にポ
リアリレート樹脂、更にはシリコーン変性ポリカーボネ
ート樹脂とを同時に含有させることで、前記課題を解決
させることが可能となった。The above problem can be solved by allowing the electrophotographic photosensitive member according to the present invention to simultaneously contain a polyarylate resin and a silicone-modified polycarbonate resin in the surface layer.
【0010】ポリアリレート樹脂は、特開平10−20
519号公報や特開平10−20523号公報等に記載
されており、これら公報にも述べられている様に、機械
的な耐磨耗性に優れる熱可塑性樹脂である。すなわち、
帯電の振動電界がかかってもその表面の粗れの発生が少
ないため、トナーの付着が抑制されると考えられる。一
方、本発明におけるシリコーン変性ポリカーボネートは
特開平6−295075号公報等に記載されているよう
に、優れた潤滑性を有するということから、更にトナー
の付着を防止する優れた効果を発していると考えられ
る。The polyarylate resin is disclosed in JP-A-10-20.
As described in JP-A No. 519 and JP-A No. 10-20523, and as described in these publications, it is a thermoplastic resin having excellent mechanical abrasion resistance. That is,
Even if an oscillating electric field for charging is applied, the occurrence of surface roughness is small, and it is considered that toner adhesion is suppressed. On the other hand, since the silicone-modified polycarbonate of the present invention has excellent lubricity as described in JP-A-6-295075, etc., it has an excellent effect of preventing toner adhesion. Conceivable.
【0011】次に、このクリーナーレス方式の電子写真
装置について、図1を用いて説明する。図1において
は、帯電ローラーにマイナスのDC電圧とAC電圧を同
時に印加し感光ドラムをマイナスに帯電し、レーザー光
により静電潜像を書き込み、マイナスに帯電した現像剤
を現像装置により感光ドラム上の露光部に現像する、反
転現像方式の例を示した。Next, the cleanerless type electrophotographic apparatus will be described with reference to FIG. In FIG. 1, negative DC voltage and AC voltage are simultaneously applied to the charging roller to negatively charge the photosensitive drum, an electrostatic latent image is written by laser light, and the negatively charged developer is applied to the photosensitive drum by the developing device. An example of the reversal development method in which development is performed on the exposed portion of
【0012】図1において、まず感光ドラム1は矢印の
方向に回転し、帯電装置(帯電ローラー)2により帯電
処理される。その後、露光手段3により画像情報が静電
潜像として書き込まれ、現像装置4によりトナー像とし
て顕像化される。顕像化された感光ドラム上のトナー像
は、転写装置(転写ローラー)5により転写材6に転写
され、その後転写材6は不図示の定着装置へと搬送され
る。転写行程後、電子写真感光体1上に残った残留トナ
ーは、補助帯電装置7により帯電と同極性でかつより高
い電位に帯電され、上記帯電行程において交流による除
電が行われる。そして露光行程を通過した後、現像装置
により現像容器内に回収され、再び現像処理に用いられ
る。以後上記の行程が繰り返される。図1に記載されて
いる補助帯電手段は、固定のブラシ状部材を用いたが、
ブラシ回転体、弾性ローラー体又はシート状部材等の任
意の形態の部材にすることができる。また、この部材
は、電子写真感光体に対してその長手方向にスラストさ
せ、電位付与性をより均一にさせることもできる。In FIG. 1, the photosensitive drum 1 first rotates in the direction of the arrow and is charged by a charging device (charging roller) 2. After that, the image information is written as an electrostatic latent image by the exposure unit 3 and visualized as a toner image by the developing device 4. The visualized toner image on the photosensitive drum is transferred to a transfer material 6 by a transfer device (transfer roller) 5, and then the transfer material 6 is conveyed to a fixing device (not shown). After the transfer step, the residual toner remaining on the electrophotographic photosensitive member 1 is charged by the auxiliary charging device 7 to the same polarity as that of the charging and to a higher potential, and the charge is removed by alternating current in the charging step. After passing through the exposure process, it is collected in the developing container by the developing device and used again for the developing process. Thereafter, the above process is repeated. The auxiliary charging means shown in FIG. 1 uses a fixed brush-shaped member,
It may be a member of any form such as a brush rotating body, an elastic roller body or a sheet-like member. Further, this member can be made to thrust the electrophotographic photosensitive member in the longitudinal direction thereof to make the potential imparting property more uniform.
【0013】更に、補助帯電手段として現像剤を帯電す
る現像剤帯電量制御手段(上述の補助帯電装置7)より
上流、かつ転写手段より下流に残留現像剤像を均一化す
る残留現像剤像均一化手段としての補助帯電装置8を追
加することもできる。図2は補助帯電装置を2つ有する
電子写真装置を示す。Further, the residual developer image is uniformed upstream of the developer charge amount control means (the above-mentioned auxiliary charging device 7) for charging the developer as the auxiliary charging means and downstream of the transfer means. It is also possible to add an auxiliary charging device 8 as a charging means. FIG. 2 shows an electrophotographic apparatus having two auxiliary charging devices.
【0014】補助帯電手段(残留現像剤像均一化手段)
8の部材にはこの図では固定のブラシ状部材を用いた
が、ブラシ回転体、弾性ローラー体又はシート状部材等
の任意の形態の部材にすることができる。また、この部
材は電子写真感光体に対してその長手方向にスラストさ
せ、電位付与性をより均一にさせることもできる。更
に、補助帯電装置7は接地させても、必要に応じてバイ
アスを印加させることもできる。Auxiliary charging means (means for uniforming residual developer image)
Although a fixed brush-like member is used for the member 8 in this figure, it may be any member such as a brush rotating body, an elastic roller body, or a sheet-like member. Further, this member can be thrust in the longitudinal direction of the electrophotographic photosensitive member to make the potential imparting property more uniform. Furthermore, the auxiliary charging device 7 can be grounded or a bias can be applied as necessary.
【0015】次に、本発明に係わる電子写真感光体につ
いて詳しく説明する。Next, the electrophotographic photosensitive member according to the present invention will be described in detail.
【0016】本発明に係る電子写真感光体として、電荷
輸送層と電荷発生層に分離した積層型で、表面層は電荷
輸送層であるものについて図3を用いて説明する。この
電子写真感光体には、導電性支持体11の上に干渉縞防
止等を目的とする下引き層13、電荷発生層14、電荷
輸送層15が順に設けられている。また、導電性支持体
11と下引き層13の間に導電層12を設けてもよい。As the electrophotographic photosensitive member according to the present invention, a laminated type in which a charge transport layer and a charge generation layer are separated and the surface layer is a charge transport layer will be described with reference to FIG. In this electrophotographic photosensitive member, an undercoat layer 13, a charge generation layer 14, and a charge transport layer 15 for the purpose of preventing interference fringes and the like are sequentially provided on a conductive support 11. Further, the conductive layer 12 may be provided between the conductive support 11 and the undercoat layer 13.
【0017】使用する支持体は、導電性を有するもので
あればよく、アルミニウム、ステンレス等の金属、ある
いは導電層を設けた金属、紙及びプラスチック等が挙げ
られ、形状はシート状や円筒状等が挙げられる。The support to be used may be any one having conductivity, and examples thereof include metals such as aluminum and stainless steel, metals provided with a conductive layer, paper, plastic, and the like, and the shape is a sheet or a cylinder. Is mentioned.
【0018】支持体の傷を被覆することを目的とした導
電層を設けてもよい。これは、カーボンブラック、金属
粒子等の導電性粉体を結着樹脂に分散させて形成するこ
とができる。導電層の膜厚は5〜40μmが好ましく、
特には10〜30μmが好ましい。A conductive layer may be provided for the purpose of covering scratches on the support. This can be formed by dispersing a conductive powder such as carbon black or metal particles in a binder resin. The thickness of the conductive layer is preferably 5 to 40 μm,
Particularly, 10 to 30 μm is preferable.
【0019】その上に接着機能を有する下引き層を設け
る。下引き層の材料としては、ポリアミド、ポリビニル
アルコール、ポリエチレンオキシド、エチルセルロー
ス、カゼイン、ポリウレタン及びポリエーテルウレタン
等が挙げられる。これらは、適当な溶剤に溶解して塗布
される。下引き層の膜厚は0.05〜5μmが好まし
く、特には0.3〜1μmが好ましい。An undercoat layer having an adhesive function is provided thereon. Examples of the material of the undercoat layer include polyamide, polyvinyl alcohol, polyethylene oxide, ethyl cellulose, casein, polyurethane and polyether urethane. These are dissolved in a suitable solvent and applied. The thickness of the undercoat layer is preferably 0.05 to 5 μm, and particularly preferably 0.3 to 1 μm.
【0020】下引き層の上には電荷発生層が形成され
る。本発明に用いられる電荷発生層としては、電荷発生
材料及び結着樹脂を溶剤中に分散させた塗料を塗工乾燥
して形成する。機能分離型の場合、電荷発生層は電荷発
生材料を結着剤樹脂及び溶剤と共にホモジナイザー、超
音波分散、ボールミル、振動ボールミル、サンドミル、
アトライター、ロールミル又は液衝突型高速分散機等の
方法で均一に分散する。ここで用いる電荷発生材料とし
ては、ピリリウム、チアピリリウム系染料、フタロシア
ニン、アントアントロン、ジベンズピレンキノン、トリ
スアゾ、シアニン、ジスアゾ、モノアゾ、インジゴ、キ
ナクリドン及び非対称キノシアニン系の各顔料が挙げら
れる。A charge generation layer is formed on the undercoat layer. The charge generation layer used in the present invention is formed by applying and drying a coating material in which a charge generation material and a binder resin are dispersed in a solvent. In the case of the function separation type, the charge generation layer includes a charge generation material together with a binder resin and a solvent, a homogenizer, ultrasonic dispersion, a ball mill, a vibrating ball mill, a sand mill,
Disperse evenly by a method such as an attritor, a roll mill or a liquid collision type high speed disperser. Examples of the charge generating material used here include pyrylium, thiapyrylium dye, phthalocyanine, anthanthrone, dibenzpyrenequinone, trisazo, cyanine, disazo, monoazo, indigo, quinacridone and asymmetric quinocyanine pigments.
【0021】結着樹脂としては、例えば、ポリエステル
樹脂、ポリアクリル樹脂、ポリビニルカルバゾール樹
脂、フェノキシ樹脂、ポリカーボネート樹脂、ポリスチ
レン樹脂、ポリビニルアセテート樹脂、ポリサルフォン
樹脂、ポリアリレート樹脂、塩化ビニルデン、ポリビニ
ルベンザール樹脂及びポリブチラール樹脂等が挙げられ
る。顔料と結着樹脂の比率は1/0.1〜1/10が好
ましく、より好ましくは1/1〜3/1である。分散液
を塗布、乾燥させて形成される電荷発生層の膜厚は5μ
m以下が好ましく、特には0.1〜2μmが好ましい。Examples of the binder resin include polyester resin, polyacrylic resin, polyvinylcarbazole resin, phenoxy resin, polycarbonate resin, polystyrene resin, polyvinyl acetate resin, polysulfone resin, polyarylate resin, vinyldene chloride, polyvinylbenzal resin, and the like. Examples thereof include polybutyral resin. The ratio of the pigment to the binder resin is preferably 1 / 0.1 to 1/10, more preferably 1/1 to 3/1. The thickness of the charge generation layer formed by coating and drying the dispersion is 5μ.
m or less is preferable, and 0.1 to 2 μm is particularly preferable.
【0022】電荷輸送層は、主として電荷輸送材料と結
着樹脂としての本発明のポリアリレート樹脂、更にはポ
リアリレート樹脂とシリコーン変性ポリカーボネートと
をこれらを溶解させる適当な溶媒に溶解させた塗料を塗
工/乾燥して形成する。The charge transport layer is mainly coated with a coating material prepared by dissolving the charge transport material and the polyarylate resin of the present invention as a binder resin, and further, dissolving the polyarylate resin and the silicone-modified polycarbonate in a suitable solvent that dissolves them. Work / dry to form.
【0023】本発明のポリアリレートの構成例として
は、特開平10−20519号公報や特開平10−20
523号公報等に記載されており、これらの例を以下に
示すが、これらに限定されるものではないが、本発明で
は構成単位例6で表わされる構造のものが好ましい。Examples of the constitution of the polyarylate of the present invention include JP-A-10-20519 and JP-A-10-20.
Examples of these are described below, but the present invention is not limited to these, and those having the structure represented by Structural Unit Example 6 are preferable in the present invention.
【0024】[0024]
【化3】 [Chemical 3]
【0025】本発明に用いられるシリコーン変性ポリカ
ーボネートにおいて式(2)で示される構成単位を有す
る重合体と式(2)、(3)及び(4)で示される構成
単位を有する共重合体の割合は、耐ソルベントクラック
性、耐久性及び電気特性に対する環境安定性、溶液安定
性に依存する製造安定性を考慮して制御しなければなら
ないが、式(2)、(3)及び(4)で示される構成単
位を有する共重合体が式(2)で示される構成単位を有
する重合体に対して質量割合で0.1〜95質量%の範
囲で有ることが好ましく、0.5〜80質量%の範囲が
特に好ましい。In the silicone-modified polycarbonate used in the present invention, the proportion of the polymer having the constitutional unit represented by the formula (2) and the copolymer having the constitutional units represented by the formulas (2), (3) and (4). Must be controlled in consideration of solvent crack resistance, environmental stability with respect to durability and electrical characteristics, and manufacturing stability depending on solution stability. However, in equations (2), (3) and (4), The copolymer having the structural unit shown is preferably in the range of 0.1 to 95% by mass with respect to the polymer having the structural unit represented by the formula (2), and 0.5 to 80% by mass. The range of% is particularly preferable.
【0026】特に、式(2)及び(3)で示される構成
単位の質量をαとし、式(4)で示される構成単位をβ
とした時にβ/(α+β)の値が0.01〜0.1の範
囲である時は、前記重合体の割合は1〜15質量%の範
囲であることが好ましく、3〜10質量%の範囲が特に
好ましい。In particular, let α be the mass of the constitutional units represented by the formulas (2) and (3), and β be the constitutional unit represented by the formula (4).
When the value of β / (α + β) is in the range of 0.01 to 0.1, the proportion of the polymer is preferably in the range of 1 to 15% by mass and 3 to 10% by mass. Ranges are particularly preferred.
【0027】また、式(2)及び(4)で示される構成
単位の質量をγとし、式(3)で示される構成単位をδ
とした時にδ/(γ+δ)の値が0.3〜0.8の範囲
であることが好ましく、0.4〜0.8の範囲が特に好
ましい。The mass of the constitutional units represented by the formulas (2) and (4) is γ, and the constitutional unit represented by the formula (3) is δ.
The value of δ / (γ + δ) is preferably 0.3 to 0.8, particularly preferably 0.4 to 0.8.
【0028】[0028]
【化4】 [Chemical 4]
【0029】本発明においてポリアリレート樹脂とシリ
コーン変性ポリカーボネート樹脂とを混合する場合はそ
れぞれの質量をA、Bとした時、A/B≧1とすること
が好ましい。When the polyarylate resin and the silicone-modified polycarbonate resin are mixed in the present invention, it is preferable that A / B ≧ 1 when the masses of A and B are A and B, respectively.
【0030】シリコーン変性ポリカーボネートは発泡性
を持っているため、混合量を多くして行くと成膜が上手
く出来なくなってしまうので上記混合比の範囲で使用す
ることが好ましい。Since the silicone-modified polycarbonate has a foaming property, if the mixing amount is increased, the film formation cannot be successful, so that it is preferable to use within the above mixing ratio range.
【0031】本発明に用いられる電荷輸送材料として
は、トリアリールアミン系化合物、ヒドラゾン化合物、
スチルベン化合物、ピラゾリン系化合物、オキサゾール
系化合物、トリアリールメタン系化合物、チアゾール系
化合物等の低分子化合物が挙げられる。電荷輸送層の結
着としては、本発明のポリアリレート樹脂とシリコーン
変性ポリカーボネートの他に、ポリカーボネート樹脂を
ブレンドしたり、その他の樹脂、例えば、ポリアクリレ
ート樹脂、ポリエステル樹脂、ポリスチレン樹脂、スチ
レン−アクリルニトリル共重合体樹脂、ポリメタクリル
酸エステル樹脂又はスチレン−メタクリル酸エステル共
重合体樹脂等を更に混合してもよい。As the charge transport material used in the present invention, triarylamine compounds, hydrazone compounds,
Examples thereof include low molecular weight compounds such as stilbene compounds, pyrazoline compounds, oxazole compounds, triarylmethane compounds and thiazole compounds. As the binding of the charge transport layer, in addition to the polyarylate resin of the present invention and the silicone-modified polycarbonate, a polycarbonate resin is blended, or other resins such as polyacrylate resin, polyester resin, polystyrene resin, styrene-acrylonitrile. You may further mix a copolymer resin, a polymethacrylic acid ester resin, a styrene-methacrylic acid ester copolymer resin, or the like.
【0032】電荷輸送材は、0.5〜2倍量の結着樹脂
と組み合わされ塗工、乾燥し、電荷輸送層を形成する。
電荷輸送層の膜厚は5〜40μmが好ましく、特には1
5〜30μmが好ましい。The charge transport material is combined with 0.5 to 2 times the amount of the binder resin, coated and dried to form the charge transport layer.
The thickness of the charge transport layer is preferably 5 to 40 μm, and particularly 1
It is preferably 5 to 30 μm.
【0033】本発明の電子写真感光体の表面層に用いら
れるシリコーン系粉末潤滑材としては、電子写真感光体
の表面の滑り性を向上させ、電子写真特性を悪化させな
いものであればどのようなものを使ってもかまわない
が、特には東亞合成化学工業(株)製の「商品名:アロ
ンGS−101CP」が好ましい。The silicone powder lubricant used in the surface layer of the electrophotographic photosensitive member of the present invention may be any one as long as it improves the slipperiness of the surface of the electrophotographic photosensitive member and does not deteriorate the electrophotographic characteristics. The product may be used, but "Product Name: Aron GS-101CP" manufactured by Toagosei Kagaku Kogyo Co., Ltd. is particularly preferable.
【0034】更に、電荷輸送層中には酸化防止剤、紫外
線吸収剤及び可塑剤等の添加剤を必要に応じ添加するこ
ともできる。Further, additives such as an antioxidant, an ultraviolet absorber and a plasticizer may be added to the charge transport layer if necessary.
【0035】[0035]
【実施例】以下に、具体的な実施例を挙げて本発明をよ
り詳細に説明する。なお、実施例中の「部」は質量部を
示す。EXAMPLES The present invention will be described in more detail below with reference to specific examples. In addition, "part" in an Example shows a mass part.
【0036】(実施例1)図1は本発明における電子写
真装置の断面図である。本実施例における電子写真装置
は、マイナスのDC電圧にAC電圧を重畳した電圧を帯
電ローラーに印加し感光ドラムをマイナスに帯電するA
C帯電装置を用い、レーザー光により静電潜像を書き込
み、マイナスに帯電したトナーを現像装置により感光ド
ラム上の露光部に現像する反転現像方式の電子写真装置
において、上記現像剤帯電制御手段7に導電性ブラシを
用いたものである。しかし、機能としてはトナーの電荷
を正規側に制御できればよいので、表面性や抵抗均一性
は要求されず、構造は簡単なものでよい。本実施例では
導電性レーヨンを使用した。この導電性ブラシには、電
源によりマイナスのDC電圧Vtcが印加してあり感光
ドラム表面に向かって放電するようになっている。転写
行程後、電子写真感光体1上に残った転写残トナーは、
導電性ブラシからの放電又は導電性ブラシとの摺擦・接
触により正規の帯電極性であるマイナスに帯電し、現像
剤帯電制御行程を通過する。導電性ブラシにはプラスト
ナーが付着するが、トナーの帯電極性を正規側に制御す
る機能にはあまり影響しない。導電性ブラシに印加する
電圧Vtcの範囲は、現像剤帯電制御行程にはいる前の
表面電位をVdbとした場合VtcはVdbよりもマイ
ナス側であること、
Vdb>Vtc
現像剤帯電制御行程にて放電を受けた後の表面電位をV
daとした場合、Vdaがその下流にある帯電行程にお
いて得たい電位Vdに収束できる範囲にあること、とい
う2つの条件により決まる。後者の条件は、帯電装置の
種類により次のようになる。本実施例のように、帯電装
置がDC電圧にAC電圧を重畳させた電圧を帯電ローラ
ーに印加するAC帯電装置の場合、現像剤帯電制御行程
後の感光ドラムの表面電位Vdaが得たい電位Vdより
プラス側であろうとマイナス側であろうと、帯電行程に
おいて電位Vdに収束させることができるので、印加電
圧Vtcには上記
Vdb>Vtc
以外に特に制限はない。(Embodiment 1) FIG. 1 is a sectional view of an electrophotographic apparatus according to the present invention. In the electrophotographic apparatus in this embodiment, a voltage obtained by superimposing an AC voltage on a negative DC voltage is applied to the charging roller to negatively charge the photosensitive drum A.
In the reversal development type electrophotographic apparatus in which an electrostatic latent image is written by a laser beam using a C charging device, and negatively charged toner is developed on an exposed portion on a photosensitive drum by a developing device, the developer charging control means 7 is used. It uses a conductive brush. However, as the function, it is sufficient that the charge of the toner can be controlled to the normal side, so that the surface property and the resistance uniformity are not required, and the structure may be simple. In this example, conductive rayon was used. A negative DC voltage Vtc is applied to the conductive brush by a power source so that the conductive brush is discharged toward the surface of the photosensitive drum. After the transfer process, the transfer residual toner remaining on the electrophotographic photosensitive member 1 is
The discharge from the conductive brush or the rubbing / contact with the conductive brush charges the developer to a negative charge, which is a regular charge polarity, and passes through the developer charge control process. Although positive toner adheres to the conductive brush, it does not affect the function of controlling the charging polarity of the toner to the regular side. The range of the voltage Vtc applied to the conductive brush is that Vtc is on the negative side of Vdb when the surface potential before entering the developer charge control step is Vdb. Vdb> Vtc In the developer charge control step The surface potential after being discharged is V
In the case of da, it is determined by two conditions that Vda is in a range where it can converge to the potential Vd desired to be obtained in the charging process downstream thereof. The latter condition is as follows depending on the type of charging device. When the charging device is an AC charging device that applies a voltage obtained by superimposing an AC voltage on a DC voltage to the charging roller as in this embodiment, the surface potential Vda of the photosensitive drum after the developer charging control process is the desired potential Vd. Regardless of the positive side or the negative side, the potential Vd can be converged in the charging process, and therefore the applied voltage Vtc is not particularly limited except Vdb> Vtc.
【0037】本実施例では、次のような電圧設定におい
て実験を行った。In this example, an experiment was conducted under the following voltage settings.
【0038】帯電装置の印加電圧;DC−600V+A
C1000〜2500Vpp
帯電行程後の表面電位Vd;−600V
露光後の表面電位Vl;−600V
現像スリーブの印加電圧Vdev;DC−400V
転写ローラーの印加電圧Vt;DC+1000V
現像剤帯電制御行程前の表面電位Vdb;+100〜−
500V
導電性ブラシ(現像剤帯電量制御手段)の印加電圧Vt
c;DC−1200V
導電性ブラシ(現像剤帯電量制御手段)の帯電開始電圧
Vth;600V
現像剤帯電制御行程後の表面電位Vda;−800VVoltage applied to the charging device: DC-600V + A
C1000 to 2500Vpp Surface potential Vd after charging process; -600V Surface potential after exposure Vl; -600V Applied voltage to developing sleeve Vdev; DC-400V Applied voltage to transfer roller Vt; DC + 1000V Surface potential Vdb before developer charging control process + 100 ~-
Applied voltage Vt of 500V conductive brush (developer charge amount control means)
c; DC-1200V Charge start voltage Vth of conductive brush (developer charge amount control means); 600V Surface potential Vda after developer charge control process; -800V
【0039】本発明における電子写真感光体はアルミニ
ウムシリンダーを支持体とし、それに、以下の材料より
構成される塗料を支持体上に浸漬法で塗布し、140℃
で30分間熱硬化し、膜厚が15μmの導電層を形成し
た。The electrophotographic photosensitive member of the present invention uses an aluminum cylinder as a support, and a coating material composed of the following materials is applied to the support by a dipping method, and the temperature is 140 ° C.
And heat-cured for 30 minutes to form a conductive layer having a thickness of 15 μm.
【0040】 導電性顔料:SnO2コート処理硫酸バリウム 10部 抵抗調節用顔料:酸化チタン 2部 結着樹脂:フェノール樹脂 6部 レベリング材:シリコーンオイル 0.001部 溶剤:メタノール/メトキシプロパノール(質量比0.2/0.8) 20部Conductive pigment: SnO 2 coated barium sulfate 10 parts Resistance adjusting pigment: titanium oxide 2 parts Binder resin: phenol resin 6 parts Leveling material: silicone oil 0.001 part Solvent: methanol / methoxy propanol (mass ratio 0.2 / 0.8) 20 parts
【0041】次に、この上にN−メトキシメチル化ナイ
ロン4.5部及び共重合ナイロン1.5部をメタノール
65部/n−ブタノール30部の混合溶媒に溶解した溶
液を浸漬法で塗布し、膜厚が0.6μmの中間層を形成
した。Next, a solution prepared by dissolving 4.5 parts of N-methoxymethylated nylon and 1.5 parts of copolymerized nylon in a mixed solvent of 65 parts of methanol / 30 parts of n-butanol was applied onto this by a dipping method. An intermediate layer having a film thickness of 0.6 μm was formed.
【0042】次に、CuKα特性X線回折におけるブラ
ッグ角(2θ±0.2°)の7.4°及び28.2°に
強いピークを有するヒドロキシガリウムフタロシアニン
結晶3.5部とポリビニルブチラール樹脂(商品名:エ
スレックBH−S、積水化学工業社製)1部をシクロヘ
キサノン120部に添加し、1mmφガラスビーズを用
いたサンドミルで3時間分散し、これにメチルエチルケ
トン120部を加えて希釈して電荷発生層用塗料を調製
した。下引き層上に、この電荷発生層用塗料を浸漬塗布
し、100℃で10分間乾燥して、膜厚0.15μmの
電荷発生層を形成した。Next, 3.5 parts of hydroxygallium phthalocyanine crystal having strong peaks at Bragg angles (2θ ± 0.2 °) of 7.4 ° and 28.2 ° in CuKα characteristic X-ray diffraction and polyvinyl butyral resin ( (Product name: S-REC BH-S, manufactured by Sekisui Chemical Co., Ltd.) 1 part was added to 120 parts of cyclohexanone and dispersed for 3 hours in a sand mill using 1 mmφ glass beads, and 120 parts of methyl ethyl ketone was added to dilute it to generate a charge A layer coating was prepared. This charge generation layer coating material was applied onto the undercoat layer by dip coating and dried at 100 ° C. for 10 minutes to form a charge generation layer having a thickness of 0.15 μm.
【0043】次に、下記式(5)で示されるの電荷輸送
材8部Next, 8 parts of the charge transport material represented by the following formula (5)
【0044】[0044]
【化5】
及び前記式(1)で示されるポリアリレート樹脂(重量
平均分子量Mw=11万)10部をジメトキシメタン3
3部/モノクロロベンゼン60部の混合溶媒に溶解させ
て電荷輸送層用塗布液とした。[Chemical 5] And 10 parts of the polyarylate resin represented by the above formula (1) (weight average molecular weight Mw = 110,000) with dimethoxymethane 3
It was dissolved in a mixed solvent of 3 parts / 60 parts of monochlorobenzene to obtain a charge transport layer coating liquid.
【0045】この塗料で浸漬法で塗布(塗布速度一定)
し、120℃で1時間乾燥し、膜厚が20μm(中心付
近)の電荷輸送層を形成した。Coating with this coating by dipping method (constant coating speed)
Then, it was dried at 120 ° C. for 1 hour to form a charge transport layer having a film thickness of 20 μm (near the center).
【0046】この様にして作製した電子写真感光体を上
述の電子写真装置に装着し、30℃/80%の環境下に
おいて帯電装置の印加電圧のAC電圧を1000、12
50、1500、2000及び2500Vp−pの5段
階に変化させて、それぞれの条件で5000枚の通紙耐
久を行い、ドラム上のトナー融着とトナー回収性に起因
するかぶりの評価を行った。結果は表1に示す。なお評
価は、トナー融着においては、○:問題なし、△:耐久
中にトナー融着発生、×:初期数枚でトナー融着発生、
カブリにおいては、○:問題なし、△:耐久中にカブリ
発生、×:初期数枚からカブリ発生で行った。The electrophotographic photosensitive member thus produced was mounted on the above-mentioned electrophotographic apparatus, and the AC voltage applied to the charging device was set to 1000 or 12 in an environment of 30 ° C./80%.
It was changed to five levels of 50, 1500, 2000 and 2500 Vp-p, and 5000 sheets were passed under each condition, and fogging due to toner fusion on the drum and toner recoverability was evaluated. The results are shown in Table 1. In the evaluation, in toner fusion, ◯: no problem, Δ: toner fusion occurred during durability, ×: toner fusion occurred in the initial several sheets,
Regarding fogging, ◯: no problem, Δ: fogging occurred during durability, ×: fogging occurred from the initial several sheets.
【0047】(実施例2)実施例1において電荷輸送材
を下記式(6)の化合物に代えた以外は、実施例1と同
様にして電子写真感光体を作製し、実施例1と同様な設
定として評価を行った。結果は表1に示す。Example 2 An electrophotographic photosensitive member was prepared in the same manner as in Example 1 except that the charge transporting material in Example 1 was replaced by the compound of the following formula (6). The setting was evaluated. The results are shown in Table 1.
【0048】[0048]
【化6】 [Chemical 6]
【0049】(実施例3)実施例1においてポリアリレ
ート樹脂を9.5部と上記式(2)、(3)、(4)で
示されるシリコーン変性ポリカーボネート(粘度平均分
子量Mv=4万)0.5部とした以外は、実施例1と同
様にして電子写真感光体を作製し、実施例1と同様な設
定として評価を行った。結果は表1に示す。(Example 3) 9.5 parts of polyarylate resin in Example 1 and the silicone-modified polycarbonate represented by the above formulas (2), (3) and (4) (viscosity average molecular weight Mv = 40,000) 0 An electrophotographic photosensitive member was produced in the same manner as in Example 1 except that the amount was set to 0.5 part, and the same settings as in Example 1 were evaluated. The results are shown in Table 1.
【0050】(実施例4)実施例3においてシリコーン
系粉末潤滑材(商品名:アロンGS−101CP、東亞
合成化学工業(株)製)を0.1部添加した以外は、実
施例1と同様にして電子写真感光体を作製し、実施例1
と同様な設定として評価を行った。結果は表1に示す。(Example 4) The same as Example 1 except that 0.1 part of the silicone powder lubricant (trade name: Aron GS-101CP, manufactured by Toagosei Chemical Industry Co., Ltd.) was added in Example 3. To prepare an electrophotographic photosensitive member, and
Evaluation was performed with the same setting as. The results are shown in Table 1.
【0051】(実施例5)実施例4において式(5)で
示される電荷輸送材を7.2部、式(6)で示される電
荷輸送材を0.8部とした以外は、実施例1と同様にし
て電子写真感光体を作製し、実施例1と同様な設定とし
て評価を行った。結果は表1に示す。Example 5 Example 5 is the same as Example 4, except that the charge transport material represented by the formula (5) was changed to 7.2 parts and the charge transport material represented by the formula (6) was changed to 0.8 part. An electrophotographic photosensitive member was produced in the same manner as in Example 1 and evaluated in the same setting as in Example 1. The results are shown in Table 1.
【0052】(実施例6)実施例5においてポリアリレ
ート樹脂を8部、シリコーン変性ポリカーボネートの含
有量を2部した以外は、実施例1と同様にして電子写真
感光体を作製し、実施例1と同様な設定として評価を行
った。結果は表1に示す。Example 6 An electrophotographic photoreceptor was prepared in the same manner as in Example 1 except that 8 parts of polyarylate resin and 2 parts of silicone-modified polycarbonate were used in Example 5. Evaluation was performed with the same setting as. The results are shown in Table 1.
【0053】(実施例7)実施例5においてポリアリレ
ート樹脂を5部、シリコーン変性ポリカーボネートの含
有量を5部した以外は、実施例1と同様にして電子写真
感光体を作製し、実施例1と同様な設定として評価を行
った。結果は表1に示す。Example 7 An electrophotographic photoreceptor was prepared in the same manner as in Example 1 except that 5 parts of polyarylate resin and 5 parts of silicone-modified polycarbonate were used in Example 5. Evaluation was performed with the same setting as. The results are shown in Table 1.
【0054】(実施例8)実施例5においてポリアリレ
ート樹脂を9.5部と上記式(2)、(3)、(4)で
示されるシリコーン変性ポリカーボネート(粘度平均分
子量Mv=4万)0.5部とした以外は、実施例1と同
様にして電子写真感光体を作製し、実施例1と同様な設
定として評価を行った。結果は表1に示す。Example 8 In Example 5, 9.5 parts of the polyarylate resin and the silicone-modified polycarbonate represented by the above formulas (2), (3) and (4) (viscosity average molecular weight Mv = 40,000) were used. An electrophotographic photosensitive member was produced in the same manner as in Example 1 except that the amount was set to 0.5 part, and the same settings as in Example 1 were evaluated. The results are shown in Table 1.
【0055】(実施例9)図2に示すような残留現像剤
均一化手段としてブラシ状部材を用いた補助帯電手段8
を有する電子写真装置を用い、実施例5の電子写真感光
体を用いて実施例1と同様な評価を行った。(Embodiment 9) Auxiliary charging means 8 using a brush-like member as a residual developer uniformizing means as shown in FIG.
The same evaluation as in Example 1 was performed using the electrophotographic apparatus of Example 5 and the electrophotographic photosensitive member of Example 5.
【0056】補助帯電手段(残留現像剤均一化手段)の
部材は、導電性レーヨンのブラシ状部材を用い、接地し
ている。結果は表1に示す。As a member of the auxiliary charging means (residual developer uniformizing means), a conductive rayon brush member is grounded. The results are shown in Table 1.
【0057】(比較例1)実施例1においてポリアリレ
ート樹脂をポリカーボネートA(商品名:テイジンパン
ライトL−1250、帝人化成(株)製)に代えた以外
は、実施例1と同様にして電子写真感光体を作製し、実
施例1と同様な設定として評価を行った。結果は表1に
示す。(Comparative Example 1) An electron was produced in the same manner as in Example 1 except that the polyarylate resin in Example 1 was changed to polycarbonate A (trade name: Teijin Panlite L-1250, manufactured by Teijin Chemicals Ltd.). A photographic photosensitive member was produced and evaluated under the same settings as in Example 1. The results are shown in Table 1.
【0058】(比較例2)実施例5においてポリアリレ
ート樹脂をポリカーボネートA(商品名:テイジンパン
ライトL−1250、帝人化成(株)製)に代えた以外
は、実施例1と同様にして電子写真感光体を作製し、実
施例1と同様な設定として評価を行った。結果は表1に
示す。(Comparative Example 2) An electron was obtained in the same manner as in Example 1 except that the polyarylate resin in Example 5 was replaced with polycarbonate A (trade name: Teijin Panlite L-1250, manufactured by Teijin Chemicals Ltd.). A photographic photosensitive member was produced and evaluated under the same settings as in Example 1. The results are shown in Table 1.
【0059】(比較例3)実施例2においてポリアリレ
ート樹脂をポリカーボネートA(商品名:テイジンパン
ライトL−1250、帝人化成(株)製)に代えた以外
は、実施例1と同様にして電子写真感光体を作製し、実
施例1と同様な設定として評価を行った。結果は表1に
示す。(Comparative Example 3) An electron was prepared in the same manner as in Example 1 except that Polycarbonate A (trade name: Teijin Panlite L-1250, manufactured by Teijin Chemicals Ltd.) was used as the polyarylate resin in Example 2. A photographic photosensitive member was produced and evaluated under the same settings as in Example 1. The results are shown in Table 1.
【0060】[0060]
【表1】 [Table 1]
【0061】[0061]
【発明の効果】以上説明したように、本発明によれば電
子写真感光体の表面層にポリアリレート樹脂、もしくは
ポリアリレート樹脂とシリコーン変性ポリカーボネート
樹脂とを同時に含有することで、従来まで課題であった
トナー融着とかぶりの問題を両立できるクリーナーレス
システムの電子写真装置、プロセスカートリッジを提供
することが可能となった。As described above, according to the present invention, it has been a problem until now that the surface layer of an electrophotographic photoreceptor contains a polyarylate resin or a polyarylate resin and a silicone-modified polycarbonate resin at the same time. It has become possible to provide a cleaner-less system electrophotographic apparatus and a process cartridge that can solve the problems of toner fusion and fogging.
【図1】本発明の電子写真装置の概略構成を示す図であ
る。FIG. 1 is a diagram showing a schematic configuration of an electrophotographic apparatus of the present invention.
【図2】補助帯電手段を2つ有する本発明の電子写真装
置の概略構成を示す図である。FIG. 2 is a diagram showing a schematic configuration of an electrophotographic apparatus of the present invention having two auxiliary charging means.
【図3】電子写真感光体の層構成を示す図である。FIG. 3 is a diagram showing a layer structure of an electrophotographic photosensitive member.
【符号の説明】 1 電子写真感光体 2 帯電装置 3 露光手段 4 現像装置 5 転写装置 6 転写材 7 補助帯電装置(現像剤帯電量制御手段) 8 補助帯電装置(残留現像剤均一化手段) S1〜S5 バイアス電圧印加電源 11 支持体 12 導電層 13 下引き層 14 電荷発生層 15 電荷輸送層[Explanation of symbols] 1 Electrophotographic photoreceptor 2 Charging device 3 exposure means 4 Developing device 5 Transfer device 6 Transfer material 7 Auxiliary charging device (developer charge amount control means) 8 Auxiliary charging device (residual developer uniformizing means) S1 to S5 Bias voltage application power supply 11 Support 12 Conductive layer 13 Undercoat layer 14 Charge generation layer 15 Charge transport layer
───────────────────────────────────────────────────── フロントページの続き (72)発明者 辻 晴之 東京都大田区下丸子3丁目30番2号 キヤ ノン株式会社内 (72)発明者 高木 進司 東京都大田区下丸子3丁目30番2号 キヤ ノン株式会社内 (72)発明者 齊藤 宏 東京都大田区下丸子3丁目30番2号 キヤ ノン株式会社内 Fターム(参考) 2H068 AA03 AA06 BB27 BB33 FA27 FC01 2H077 AA37 AC16 AD06 AD13 AD31 AD35 DB08 GA04 2H134 GA01 GB02 HF13 KG01 KG03 KG07 KG08 KH01 MA02 MA11 MA19 2H200 FA03 FA08 FA18 GA16 GA23 GA34 GA44 GA49 GB32 GB37 HA02 HA28 HB07 HB12 HB22 HB41 HB48 JA02 JA28 JB10 NA02 NA06 ─────────────────────────────────────────────────── ─── Continued front page (72) Inventor Haruyuki Tsuji 3-30-2 Shimomaruko, Ota-ku, Tokyo Non non corporation (72) Inventor Shinji Takagi 3-30-2 Shimomaruko, Ota-ku, Tokyo Non non corporation (72) Inventor Hiroshi Saito 3-30-2 Shimomaruko, Ota-ku, Tokyo Non non corporation F-term (reference) 2H068 AA03 AA06 BB27 BB33 FA27 FC01 2H077 AA37 AC16 AD06 AD13 AD31 AD35 DB08 GA04 2H134 GA01 GB02 HF13 KG01 KG03 KG07 KG08 KH01 MA02 MA11 MA19 2H200 FA03 FA08 FA18 GA16 GA23 GA34 GA44 GA49 GB32 GB37 HA02 HA28 HB07 HB12 HB22 HB41 HB48 JA02 JA28 JB10 NA02 NA06
Claims (8)
電する帯電手段と、帯電処理された電子写真感光体に静
電潜像を形成する情報書き込み手段と、静電潜像に現像
剤を供給し静電潜像を可視化する現像手段と、可視化し
た現像剤像を転写材に転写する転写手段と、該帯電手段
より上流に位置していて、電子写真感光体面上の現像剤
を帯電する現像剤帯電量制御手段とを有し、転写工程後
の電子写真感光体上に残余する現像剤を、該現像剤帯電
量制御手段で正規極性に帯電処理し、該帯電手段で該電
子写真感光体面を帯電すると同時に、適正帯電量にする
電子写真装置において、該電子写真感光体が表面層にポ
リアリレート樹脂を含有することを特徴とする電子写真
装置。1. An electrophotographic photosensitive member, charging means for charging the electrophotographic photosensitive member, information writing means for forming an electrostatic latent image on the electrophotographic photosensitive member that has been subjected to charging processing, and a developer for the electrostatic latent image. And a transfer means for transferring the visualized developer image to a transfer material and a charging means for charging the developer on the surface of the electrophotographic photosensitive member. The developer remaining on the electrophotographic photosensitive member after the transfer step is charged to a normal polarity by the developer charge amount controlling means, and the electrophotography is performed by the charging means. An electrophotographic apparatus which charges a surface of a photoreceptor at the same time as an appropriate amount of charge, wherein the electrophotographic photoreceptor contains a polyarylate resin in a surface layer.
する現像剤帯電量制御手段より上流、かつ転写手段より
下流に位置していて、該現像剤像を転写材に転写した後
の電子写真感光体面上に残留する残留現像剤像を均一化
する残留現像剤像均一化手段を有し、現像剤像転写後の
電子写真感光体面上に残留する残留現像剤像を該残留現
像剤像均一化手段で均一化し、その均一化された電子写
真感光体面上の残留現像剤を該現像剤帯電量制御手段で
正規極性に帯電処理し、該帯電手段で電子写真感光体面
上を帯電すると同時に、適正帯電量にする請求項1に記
載の電子写真装置。2. An electron after the developer image is transferred to a transfer material, which is located upstream of the developer charge amount control means for charging the developer on the surface of the electrophotographic photosensitive member and downstream of the transfer means. A residual developer image uniformizing means for uniformizing the residual developer image remaining on the surface of the photographic photosensitive member is provided, and the residual developer image remaining on the surface of the electrophotographic photosensitive member after the transfer of the developer image is converted to the residual developer image. The residual developer on the surface of the electrophotographic photosensitive member, which is uniformized by the uniformizing means, is charged to a normal polarity by the developer charge amount controlling means, and the surface of the electrophotographic photosensitive member is charged by the charging means. The electrophotographic apparatus according to claim 1, wherein an appropriate charge amount is set.
つ振動電界を印加する請求項1又は2に記載の電子写真
装置。3. The electrophotographic apparatus according to claim 1, wherein the charging unit is of a contact charging type and applies an oscillating electric field.
(1)で示される請求項1〜3のいずれかに記載の電子
写真装置。 【化1】 4. The electrophotographic apparatus according to claim 1, wherein the structure of the polyarylate resin is represented by the following formula (1). [Chemical 1]
リカーボネート樹脂が含有されている請求項1〜4のい
ずれかに記載の電子写真装置。5. The electrophotographic apparatus according to claim 1, wherein the electrophotographic photosensitive member contains a silicone-modified polycarbonate resin.
脂が下記式(2)(3)及び(4)で示される構成単位
の共重合体である請求項5に記載の電子写真装置。 【化2】 6. The electrophotographic apparatus according to claim 5, wherein the silicone-modified polycarbonate resin is a copolymer of structural units represented by the following formulas (2), (3) and (4). [Chemical 2]
ン系粉末潤滑材を含有する請求項5に記載の電子写真装
置。7. The electrophotographic apparatus according to claim 5, wherein the surface layer of the electrophotographic photosensitive member contains a silicone powder lubricant.
手段及び現像手段からなる群より選択される少なくとも
一つの手段を共に一体に支持し、請求項1〜7のいずれ
かに記載の電子写真装置本体に着脱自在であることを特
徴とするプロセスカートリッジ。8. The electron according to claim 1, wherein the electrophotographic photosensitive member and at least one unit selected from the group consisting of a charging unit, an auxiliary charging unit and a developing unit are integrally supported. A process cartridge that is removable from the main body of the photographic device.
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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US7175955B2 (en) | 2003-06-30 | 2007-02-13 | Fuji Xerox Co., Ltd. | Electrophotographic photoreceptor, electrophotographic process cartridge and image forming apparatus |
JP2015191166A (en) * | 2014-03-28 | 2015-11-02 | 三菱化学株式会社 | Electrophotographic photoreceptor, electrophotographic photoreceptor cartridge, and image forming apparatus |
JP2021021943A (en) * | 2019-07-25 | 2021-02-18 | キヤノン株式会社 | Process cartridge and electrophotographic device |
-
2001
- 2001-07-30 JP JP2001229902A patent/JP2003043817A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7175955B2 (en) | 2003-06-30 | 2007-02-13 | Fuji Xerox Co., Ltd. | Electrophotographic photoreceptor, electrophotographic process cartridge and image forming apparatus |
JP2015191166A (en) * | 2014-03-28 | 2015-11-02 | 三菱化学株式会社 | Electrophotographic photoreceptor, electrophotographic photoreceptor cartridge, and image forming apparatus |
JP2021021943A (en) * | 2019-07-25 | 2021-02-18 | キヤノン株式会社 | Process cartridge and electrophotographic device |
JP7494030B2 (en) | 2019-07-25 | 2024-06-03 | キヤノン株式会社 | Process cartridge and electrophotographic apparatus |
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