JPH046567A - Electrophotographic method - Google Patents
Electrophotographic methodInfo
- Publication number
- JPH046567A JPH046567A JP10661390A JP10661390A JPH046567A JP H046567 A JPH046567 A JP H046567A JP 10661390 A JP10661390 A JP 10661390A JP 10661390 A JP10661390 A JP 10661390A JP H046567 A JPH046567 A JP H046567A
- Authority
- JP
- Japan
- Prior art keywords
- charging
- electrifying
- electrophotographic
- charging member
- temperature
- 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
- 238000000034 method Methods 0.000 title claims abstract description 46
- 108091008695 photoreceptors Proteins 0.000 claims description 43
- 230000002093 peripheral effect Effects 0.000 claims description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 abstract description 10
- 230000006866 deterioration Effects 0.000 abstract description 9
- 239000010410 layer Substances 0.000 description 19
- 239000000049 pigment Substances 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 11
- 239000000463 material Substances 0.000 description 10
- 239000000975 dye Substances 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 239000011241 protective layer Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- 239000004417 polycarbonate Substances 0.000 description 4
- 229920000515 polycarbonate Polymers 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000011669 selenium Substances 0.000 description 3
- 230000001235 sensitizing effect Effects 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 2
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 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
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 229920001940 conductive polymer Polymers 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 229940097275 indigo Drugs 0.000 description 2
- 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 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000012860 organic pigment Substances 0.000 description 2
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 2
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 229920001230 polyarylate Polymers 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 150000003219 pyrazolines Chemical class 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 229910052711 selenium Inorganic materials 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
- WNYHOOQHJMHHQW-UHFFFAOYSA-N 1-chloropyrene Chemical compound C1=C2C(Cl)=CC=C(C=C3)C2=C2C3=CC=CC2=C1 WNYHOOQHJMHHQW-UHFFFAOYSA-N 0.000 description 1
- IICCLYANAQEHCI-UHFFFAOYSA-N 4,5,6,7-tetrachloro-3',6'-dihydroxy-2',4',5',7'-tetraiodospiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C(C(=C(Cl)C(Cl)=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 IICCLYANAQEHCI-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000519995 Stachys sylvatica Species 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 150000001716 carbazoles Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000007857 hydrazones Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000000113 methacrylic resin Substances 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 150000002916 oxazoles Chemical class 0.000 description 1
- 229920002382 photo conductive polymer Polymers 0.000 description 1
- 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 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920001197 polyacetylene Polymers 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 229920000123 polythiophene 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
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229930187593 rose bengal Natural products 0.000 description 1
- 229940081623 rose bengal Drugs 0.000 description 1
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- PWEBUXCTKOWPCW-UHFFFAOYSA-N squaric acid Chemical compound OC1=C(O)C(=O)C1=O PWEBUXCTKOWPCW-UHFFFAOYSA-N 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- 125000005259 triarylamine group Chemical group 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
Landscapes
- Electrostatic Charge, Transfer And Separation In Electrography (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は電子写真感光体に帯電用部材を接触させて帯電
を行なう電子写真法に関し、さらに詳しくは、上記帯電
用部材の温度を比較的高温に保つことにより安定して帯
電を実施する電子写真法に関する。Detailed Description of the Invention [Field of Industrial Application] The present invention relates to an electrophotographic method in which charging is performed by bringing a charging member into contact with an electrophotographic photoreceptor, and more specifically, the present invention relates to an electrophotographic method in which charging is performed by bringing a charging member into contact with an electrophotographic photoreceptor. This invention relates to an electrophotographic method that performs stable charging by maintaining high temperatures.
[従来の技術]
従来、電子写真感光体に用いる光導電性材料として、セ
レン、硫化カドミウム、酸化亜鉛などの無機光導電性材
料が知られている。これらの光導電性材料は、数多くの
利点、例えば、暗所で適当な電位に帯電できること、暗
所で電荷の逸散が少ないこと、あるいは光照射によって
速やかに電荷を逸散できることなどの利点をもっている
反面各種の欠点を有している。例えば、セレン系感光体
では、温度、湿度、ごみ、圧力などの要因で容易に結晶
化が進み、特に雰囲気温度が40℃を越えると結晶化が
著しく成り、帯電性が低下したり画像に白い斑点が発生
するといった欠点がある。硫化カドミウム系感光体では
、多湿の環境下で安定した感度が得られないという欠点
がある。また酸化亜鉛系感光体ではローズベンガルに代
表される増感色素による増感効果を必要としているが、
このような増感色素が帯電による帯電劣化や露光光によ
る光接合を生じるため長期にわたって安定した画像を与
えることができないという欠点を有している。[Prior Art] Conventionally, inorganic photoconductive materials such as selenium, cadmium sulfide, and zinc oxide are known as photoconductive materials used in electrophotographic photoreceptors. These photoconductive materials have a number of advantages, such as being able to be charged to an appropriate potential in the dark, having little charge dissipation in the dark, or being able to quickly dissipate the charge when irradiated with light. On the other hand, it has various drawbacks. For example, in selenium-based photoreceptors, crystallization easily progresses due to factors such as temperature, humidity, dust, and pressure. Especially when the ambient temperature exceeds 40°C, crystallization occurs significantly, resulting in decreased charging properties and white images. It has the disadvantage of causing spots. Cadmium sulfide photoreceptors have the disadvantage that stable sensitivity cannot be obtained in humid environments. Furthermore, zinc oxide photoreceptors require the sensitizing effect of sensitizing dyes such as rose bengal.
Such sensitizing dyes have the disadvantage that they cannot provide stable images over a long period of time because they cause charging deterioration due to charging and photobonding due to exposure light.
一方、特定の有機化合物が光導電性を示すことが発見さ
れてきた。たとえばポリ−N−ビニルカルバゾール、ポ
リビニルアントラセンなどの有機光導電性ポリマー、カ
ルバゾール、アントラセン、ピラゾリン類、オキサジア
ゾール類、ヒドラゾン類、ボリアリールアルカン類など
の低分子の有機光導電体のばかフタロシアニン顔料、ア
ゾ顔料、シアニン染料、多環キノン顔料、ペリレン系顔
料、インジゴ染料、チオインジゴ染料あるいはスクエア
リック酸メチン染料などの有機顔料や染料が知られてい
る。特に光導電性を有する有機顔料や染料は無機材料に
比べて合成が容易で、しかも適当な波長域に光導電性を
示す化合物を選択できるバリエーションが拡大されたこ
となどから、数多く提案されている。例えば米国特許筒
4123270、同第4251613号、同第4251
614号、同第4256821号、同第4260672
号、同第4268596号、同第4278747号、同
第4293528号などに開示されているように、電荷
発生層と電荷輸送層に機能分離した感光層における電荷
発生物質として光導電性を示すジスアゾ顔料を用いた電
子写真感光体などが知られている。On the other hand, it has been discovered that certain organic compounds exhibit photoconductivity. For example, organic photoconductive polymers such as poly-N-vinylcarbazole and polyvinylanthracene, and low-molecular organic photoconductor bakaphthalocyanine pigments such as carbazole, anthracene, pyrazolines, oxadiazoles, hydrazones, and polyarylalkanes. Organic pigments and dyes such as , azo pigments, cyanine dyes, polycyclic quinone pigments, perylene pigments, indigo dyes, thioindigo dyes, and methine squaric acid dyes are known. In particular, many photoconductive organic pigments and dyes have been proposed because they are easier to synthesize than inorganic materials, and the variety of compounds that exhibit photoconductivity in an appropriate wavelength range has been expanded. . For example, U.S. Patent Nos. 4123270, 4251613, and 4251
No. 614, No. 4256821, No. 4260672
Disazo pigments that exhibit photoconductivity as a charge-generating substance in a photosensitive layer that is functionally separated into a charge-generating layer and a charge-transporting layer, as disclosed in Japanese Patent No. 4268596, No. 4278747, and No. 4293528. Electrophotographic photoreceptors using the same are known.
このような電子写真感光体を用いた電子写真プロセスに
おける帯電プロセスは、従来より殆ど金属ワイヤーに高
電圧(DC5〜8 kV)を印加し、発生するコロナに
より帯電を行なっている。しかしこの方法では、コロナ
発生時にオゾンやNOx等のコロナ生成物により感光体
表面を変質させ、画像ボケや劣化を進行させたり、ワイ
ヤーの汚わが画像品質に影響し、画像白抜けや黒スジを
生じる等の問題があった。In the charging process in an electrophotographic process using such an electrophotographic photoreceptor, a high voltage (DC 5 to 8 kV) is applied to a metal wire, and charging is performed using generated corona. However, with this method, when corona occurs, corona products such as ozone and NOx alter the surface of the photoreceptor, causing image blurring and deterioration, and dirty wires affect image quality, resulting in white spots and black lines in the image. There were some problems such as:
一方、電力的にも、感光体に向かう電流はその5〜30
%にすぎず、殆どがシールド板に流れ、帯電手段として
は効率の悪いものであった。On the other hand, in terms of electric power, the current flowing to the photoreceptor is 5 to 30
%, and most of it flowed to the shield plate, making it inefficient as a charging means.
こうした欠点を補うために従来から直接帯電させる方法
が研究され、多数提案されている(特開昭57−178
267号、同56−104351号、同5g−4056
6号、同58−139156号、同58−150975
号等)。In order to compensate for these drawbacks, direct charging methods have been researched and many proposals have been made (Japanese Patent Laid-Open No. 57-178
No. 267, No. 56-104351, No. 5g-4056
No. 6, No. 58-139156, No. 58-150975
No. etc.).
[発明が解決しようとする課題]
しかし実際には感光体を上記のような接触帯電法により
帯電処理しても、感光体表面の各部の均一な帯電はなさ
れず、斑点状帯電ムラを生じる。[Problems to be Solved by the Invention] However, in reality, even when a photoreceptor is charged by the contact charging method as described above, each part of the surface of the photoreceptor is not uniformly charged, resulting in spot-like charging unevenness.
特に環境の変化によって帯電特性が変化し、低温状態に
おいては均一な帯電はなされず、斑点状の帯電ムラが激
しくなる。また接触帯電方法に於ても帯電の際に放電が
おこり、コロナ帯電の場合よりもl/l O〜1/10
0と少ないがオゾンやNOx等が発生する。オゾンやN
Ox等は感光体及び帯電用部材を劣化させる。In particular, the charging characteristics change due to changes in the environment, and at low temperatures, uniform charging is not achieved and uneven charging becomes severe. In addition, even in the contact charging method, discharge occurs during charging, which is 1/l O to 1/10 lower than in the case of corona charging.
Ozone, NOx, etc. are generated, although the amount is small (0). Ozone and N
Ox and the like deteriorate the photoreceptor and the charging member.
本発明の目的は上述の如き欠点を解決し、温度、湿度等
の環境の変化に対しても安定した帯電特性を維持し、オ
ゾン等の影響を受けにく(する電子写真法を提供するこ
とにある。An object of the present invention is to provide an electrophotographic method that solves the above-mentioned drawbacks, maintains stable charging characteristics even with changes in the environment such as temperature and humidity, and is less susceptible to the effects of ozone, etc. It is in.
[課題を解決するための手段]
本発明の電子写真法は電子写真感光体に帯電用部材を接
触させて電圧を印加することにより該感光体表面を帯電
させる帯電プロセスを用いる電子写真法において、該帯
電用部材の温度を35℃〜55℃の範囲に維持して実施
することを特徴とする。[Means for Solving the Problems] The electrophotographic method of the present invention uses a charging process in which the surface of the photoreceptor is charged by bringing a charging member into contact with the electrophotographic photoreceptor and applying a voltage. The method is characterized in that the temperature of the charging member is maintained in the range of 35°C to 55°C.
本発明の電子写真法における直接帯電の方法は特定の方
法に限定されるものではない。帯電用部材の形状として
はローラー、ブラシ(磁気ブラシも含む)、ブレード、
ベルトなどいずれの形状であってもよく、電子写真装置
の仕様、形態にあわせて選択可能である。またこの帯電
用部材の材質として、アルミニウム、鉄、銅等の金属;
ポリアセチレン、ポリピロール、ポリチオフェン等の導
電性高分子材料;カーボン、金属等を分散させて導電性
処理したゴムや人工繊維;又はポリカーボネート、ポリ
エチレン、ポリプロピレン、ポリ塩化ビニル、ポリエチ
レンテレフタレート、アクリル樹脂等の絶縁性物質の表
面を金属や他の導電性物質によってコートしたものなど
を用いることができる。電子写真感光体に接触させるこ
れらの帯電用部材の抵抗率は良好な帯電と絶縁、破壊防
止の点から好ましくは10°〜10′2ΩCm、最適に
は10”〜10I0Ω・cmの範囲である。The method of direct charging in the electrophotographic method of the present invention is not limited to a specific method. The shapes of charging members include rollers, brushes (including magnetic brushes), blades,
It may be of any shape, such as a belt, and can be selected according to the specifications and form of the electrophotographic apparatus. Also, as the material of this charging member, metals such as aluminum, iron, copper;
Conductive polymer materials such as polyacetylene, polypyrrole, and polythiophene; Rubber and artificial fibers treated to be conductive by dispersing carbon, metal, etc.; Or insulating materials such as polycarbonate, polyethylene, polypropylene, polyvinyl chloride, polyethylene terephthalate, and acrylic resin. A material whose surface is coated with metal or other conductive material can be used. The resistivity of these charging members brought into contact with the electrophotographic photoreceptor is preferably in the range of 10 DEG to 10'2 ΩCm, and optimally 10'' to 10I0 Ω·cm, from the viewpoint of good charging, insulation, and destruction prevention.
また、電子写真感光体に絶縁破壊等の欠陥がある場合に
過剰電流が流れて電圧降下が生じるのを低減させるため
に帯電用部材の表面層をたとえばアルコキシメチル化ナ
イロンなどのような体積抵抗率106〜1012Ω・c
m程度の樹脂層として多層構成とすることもできる。特
に導電性高分子材料やアルコキシメチル化ナイロンなど
を用いた場合には低温環境下において帯電特性の低下が
起こりやすいので、それを防止するのに本発明は有効で
ある。In addition, in order to reduce the voltage drop caused by excessive current flowing when the electrophotographic photoreceptor has defects such as dielectric breakdown, the surface layer of the charging member is made of a material with a volume resistivity such as alkoxymethylated nylon. 106~1012Ω・c
It is also possible to have a multilayer structure with about m resin layers. In particular, when a conductive polymer material, alkoxymethylated nylon, or the like is used, charging characteristics tend to deteriorate in a low-temperature environment, so the present invention is effective in preventing this.
本発明の電子写真法において電子写真感光体に接触させ
る帯電用部材の設置方式についても特定の方法に限定さ
れるものではなく、帯電用部材は固定方式、あるいは電
子写真感光体と同方向または逆方向等の回転等による移
動方式のいずれの方式を用いて設置してもよい。さらに
帯電用部材を電子写真感光体上のトナークリーニング装
置として機能させることも可能である。In the electrophotographic method of the present invention, the method of installing the charging member that is brought into contact with the electrophotographic photoreceptor is not limited to a specific method, and the charging member may be fixed, or may be placed in the same direction or opposite to the electrophotographic photoreceptor. It may be installed using any method of movement, such as rotation in direction, etc. Furthermore, it is also possible for the charging member to function as a toner cleaning device on the electrophotographic photoreceptor.
本発明の電子写真法における直接帯電による帯電用部材
への印加電圧は直流、交流のいずれも採用でき、直流に
交流を重畳させた形で印加することもできる。さらにそ
の印加方法に関しては各々の電子写真装置の仕様にもよ
るが、瞬時に所望する電圧を印加する方式の他に、電子
写真感光体の保護の目的で段階的に印加電圧を上げてい
く方式、直流に交流を重畳させた形で印加の場合ならば
直流−交流または交流−直流の順序で電圧を印加する方
式をとることができる。電子写真感光体表面の各部を均
一に帯電させるために、また斑点状の帯電ムラなどを防
ぐために直流に交流を重畳させた形で印加する方式が好
ましい。The voltage applied to the charging member by direct charging in the electrophotographic method of the present invention may be either direct current or alternating current, or may be applied in the form of superimposing alternating current on direct current. Furthermore, the application method depends on the specifications of each electrophotographic device, but in addition to the method of instantaneously applying the desired voltage, there is also a method of increasing the applied voltage in stages for the purpose of protecting the electrophotographic photoreceptor. If the voltage is applied in the form of direct current and alternating current superimposed, a method can be adopted in which the voltage is applied in the order of direct current-alternating current or alternating current-direct current. In order to uniformly charge each part of the surface of the electrophotographic photoreceptor and to prevent spot-like charging unevenness, it is preferable to apply a superimposed alternating current to a direct current.
直流に交流を重畳させた形で印加する場合には、電流が
ふえるため、オゾン、NOx等の生成物が直流印加の場
合よりも多く発生し、電子写真感光体の劣化及び帯電用
部材の劣化をおこしやすいので、これを防止するのに本
発明はさらに有効である。When direct current is applied in the form of superimposed alternating current, the current increases and more products such as ozone and NOx are generated than when direct current is applied, resulting in deterioration of the electrophotographic photoreceptor and charging member. The present invention is more effective in preventing this from occurring.
また、近年複写機及びレーザープリンター等は、高速化
へとすすんでおり、速いプロセススピード(電子写真感
光体の周速)の場合には、電子写真感光体表面を均一に
帯電させるのに必要な電流が増え、その結果オゾン、N
Ox等が多く発生し、電子写真感光体の劣化、帯電用部
材の劣化を起こしやすくなり、また帯電用部材の帯電特
性の変化の影響をうけやすくなる。これを防止するのに
本発明は有効であり、特に電子写真感光体の周速(プロ
セススピード)が40 mm/sec以上である場合に
非常に有効である。In recent years, copying machines, laser printers, etc. have become faster, and in the case of high process speeds (peripheral speed of the electrophotographic photoreceptor), it is necessary to uniformly charge the surface of the electrophotographic photoreceptor. The current increases, resulting in ozone, N
A large amount of Ox, etc. is generated, which tends to cause deterioration of the electrophotographic photoreceptor and charging member, and also makes it susceptible to changes in the charging characteristics of the charging member. The present invention is effective in preventing this, and is particularly effective when the peripheral speed (process speed) of the electrophotographic photoreceptor is 40 mm/sec or more.
帯電用部材の温度は35℃〜55℃の範囲が適当である
。なぜなら35℃未満であると低温特性を良好にする効
果が薄く、また55℃を超えるとクリーナーよりすりぬ
けた現像剤(トナー)の帯電用部材及び電子写真感光体
への融着の問題がでてくるからである。The temperature of the charging member is suitably in the range of 35°C to 55°C. This is because if the temperature is below 35°C, the effect of improving low-temperature properties will be weak, and if it exceeds 55°C, there will be a problem of the developer (toner) that has slipped through the cleaner adhering to the charging member and the electrophotographic photoreceptor. This is because it comes.
帯電用部材の温度を35℃〜55℃に加温して使用する
ことにより、低温、低湿環境においての帯電不良を防止
し、環境の変化に対しても安定した性能を維持すること
ができる。また、35℃〜55℃に加温して使用するこ
とにより、放電により発生したオゾンやNOxの帯・重
用部材への付着を防ぎ、分解を促進し、帯電用部材及び
電子写真感光体の汚染、劣化を防ぐことができる。By heating the charging member to a temperature of 35° C. to 55° C., charging failures can be prevented in low-temperature, low-humidity environments, and stable performance can be maintained even under environmental changes. In addition, by heating the temperature between 35°C and 55°C, ozone and NOx generated by discharge can be prevented from adhering to the belt and heavy-duty parts, promoting decomposition, and contaminating charging parts and electrophotographic photoreceptors. , deterioration can be prevented.
本発明の電子写真法において帯電用部材を加温する手段
としてはその温度を前記の範囲とすることができる限り
任意の手段を採用し得る。例えば、帯電用部材近傍に、
又はその内部に熱源を設ける方法や、熱定着装置等から
の熱を熱源として帯電用部材を加温する手段等を採用し
得る。温度の調節はサーモスタット等の公知の温度調節
部材を使用して行なえばよい。In the electrophotographic method of the present invention, any means can be used to heat the charging member as long as the temperature can be kept within the above range. For example, near the charging member,
Alternatively, a method of providing a heat source inside the charging member, or a means of heating the charging member using heat from a heat fixing device or the like as a heat source may be adopted. The temperature may be adjusted using a known temperature adjusting member such as a thermostat.
本発明の電子写真法における電子写真感光体はSe、
CdS、アモルファスシリコンなどの無機系感光体でも
有機系感光体でもよい。例えば、有機系感光体の場合に
は、導電性支持体としてアルミニウム、アルミニウム合
金、ステンレスなどの金属;導電性物質を単独又は適当
なバインダーと共に塗布して導電層を設けた金属;ある
いは導電処理したプラスチックや紙などをドラム状又は
シート状に成形したものなど、従来公知のいずれのもの
も用いることができる。The electrophotographic photoreceptor in the electrophotographic method of the present invention is Se,
It may be an inorganic photoreceptor such as CdS or amorphous silicon, or an organic photoreceptor. For example, in the case of an organic photoreceptor, a metal such as aluminum, aluminum alloy, or stainless steel is used as the conductive support; a metal coated with a conductive substance alone or with an appropriate binder to form a conductive layer; Any conventionally known material can be used, such as a drum-shaped or sheet-shaped material made of plastic or paper.
電荷発生層は、アゾ顔料、キノン顔料、キノシアニン顔
料、ペリレン顔料、インジゴ顔料、フタロシアニン顔料
などの電荷発生物質を、ポリビニルブチラール、ポリス
チレン、アクリル樹脂、ポリエステル、ポリ酢酸ビニル
、ポリカーボネートなどの結着性樹脂に分散含有させて
形成することができ、また、真空蒸着装置によって真空
蒸着膜として形成することもできる。電荷発生層の膜厚
は0.01〜3μmが好ましい。The charge generation layer contains a charge generation substance such as an azo pigment, a quinone pigment, a quinocyanine pigment, a perylene pigment, an indigo pigment, or a phthalocyanine pigment, and a binding resin such as polyvinyl butyral, polystyrene, acrylic resin, polyester, polyvinyl acetate, or polycarbonate. It can be formed by dispersing and containing the film, or it can also be formed as a vacuum deposited film using a vacuum deposition apparatus. The thickness of the charge generation layer is preferably 0.01 to 3 μm.
電荷輸送層は、スチリル系化合物、ヒドラゾン系化合物
、トリアリールアミン系化合物、カルバゾール系化合物
、オキサゾール系化合物、ピラゾリン系化合物などの電
荷輸送物質を、ボリアリレート、ポリスチレン、アクリ
ル樹脂、ポリエステル、ポリカーボネートなどの結着性
樹脂に分散含有させて形成することができる。電荷輸送
層の好ましい膜厚は10〜30μmである。The charge transport layer contains charge transport substances such as styryl compounds, hydrazone compounds, triarylamine compounds, carbazole compounds, oxazole compounds, and pyrazoline compounds, and polyarylates, polystyrene, acrylic resins, polyesters, polycarbonates, etc. It can be formed by being dispersed in a binding resin. The preferred thickness of the charge transport layer is 10 to 30 μm.
また、感光層の構成としては電荷発生層、電荷輸送層の
順、又は、その逆に積層する。または、前述の電荷発生
物質と電荷輸送物質とを一緒に含有させた単一層型であ
ってもよい。さらに、導電性支持体と感光層との間には
、接着性及びバリヤ性を向上させるために下引き層など
の中間層を設けてもよい。Further, the structure of the photosensitive layer is such that the charge generation layer and the charge transport layer are laminated in this order, or vice versa. Alternatively, it may be a single layer type in which the charge generating material and the charge transporting material described above are contained together. Furthermore, an intermediate layer such as a subbing layer may be provided between the conductive support and the photosensitive layer in order to improve adhesiveness and barrier properties.
又、色素、顔料、有機電荷輸送物質などは、般に紫外線
、オゾン、オイルなどによる汚れ、金属などに弱いため
、必要に応じて保護層を設けてもよい。この保護層上に
静電潮像を形成するためには表面抵抗率がIQIIΩ・
0111以上であることが望ましい。Furthermore, dyes, pigments, organic charge transport substances, and the like are generally susceptible to ultraviolet rays, ozone, stains caused by oil, and metals, so a protective layer may be provided as necessary. In order to form an electrostatic tide image on this protective layer, the surface resistivity must be IQIIΩ・
It is desirable that the value is 0111 or more.
本発明で用いる保護層はポリビニルブチラール、ポリエ
ステル、ポリカーボネート、アクリル樹脂、メタクリル
樹脂、ナイロン、ポリイミド、ボリアリレート、ポリウ
レタン、スチレン−ブタジェンコポリマー、スチレン−
アクリル酸コポリマー、スチレン−アクリロニトリルコ
ポリマーなどの樹脂を適当な有機溶剤によって溶解した
液を感光層の上に塗布、乾燥して形成することができる
。この際、保護層の膜厚は、一般に0.05〜20μm
の範囲である。この保護層中に紫外線吸収剤などを含ま
せてもよい。The protective layer used in the present invention is made of polyvinyl butyral, polyester, polycarbonate, acrylic resin, methacrylic resin, nylon, polyimide, polyarylate, polyurethane, styrene-butadiene copolymer, styrene-
The photosensitive layer can be formed by applying a solution prepared by dissolving a resin such as an acrylic acid copolymer or a styrene-acrylonitrile copolymer in a suitable organic solvent onto the photosensitive layer and drying it. At this time, the thickness of the protective layer is generally 0.05 to 20 μm.
is within the range of This protective layer may contain an ultraviolet absorber or the like.
有機系感光体は、無機系感光体に比べてオゾン、NOx
等の影響をうけやすいので、これを防止するのに本発明
は特に有効である。Organic photoreceptors produce less ozone and NOx than inorganic photoreceptors.
The present invention is particularly effective in preventing this.
本発明の電子写真法は、複写機だけでなく、レーザープ
リンタ、LEDプリンタやCRTプリンター、電子写真
式製版システムなど電子写真応用分野に広く用いること
ができる。The electrophotographic method of the present invention can be widely used not only in copying machines but also in electrophotographic application fields such as laser printers, LED printers, CRT printers, and electrophotographic plate making systems.
[実施例]
次に、本発明を実施例により具体的に説明するが本発明
はこれらによって限定されるものではない。[Examples] Next, the present invention will be specifically explained with reference to Examples, but the present invention is not limited thereto.
実施例1,2.3及び比較例1.2
キヤノン製レーザビームプリンタ[レーザショットLB
P−A408]を第1図に示すように改造した。第1図
において1はレーザショット用有機感光体、2は直接帯
電を行なうための帯電用部材、3は半導体レーザ露光、
4は現像器、5は給紙ローラーと給紙ガイド、6は転写
帯電器、7はクリーナー、8は前露光である。Examples 1, 2.3 and Comparative Example 1.2 Canon laser beam printer [Laser Shot LB
P-A408] was modified as shown in FIG. In FIG. 1, 1 is an organic photoreceptor for laser shot, 2 is a charging member for direct charging, 3 is a semiconductor laser exposure member,
4 is a developing device, 5 is a paper feed roller and a paper feed guide, 6 is a transfer charger, 7 is a cleaner, and 8 is a pre-exposure.
2は本発明の電子写真法において直接帯電を実施するの
に用いる帯電用部材であり、クロロピレンゴム100重
量部に導電性カーボン5重量部を溶融混練し、中心にス
テンレス軸を通し、成型して帯電用部材とした。また帯
電用部材の近傍に熱源9を設けた。レーザビームプリン
タのプロセススピードは47 mm/seeであった。2 is a charging member used for direct charging in the electrophotographic method of the present invention, which is made by melting and kneading 100 parts by weight of chloropyrene rubber with 5 parts by weight of conductive carbon, passing a stainless steel shaft through the center, and molding. It was used as a charging member. Further, a heat source 9 was provided near the charging member. The process speed of the laser beam printer was 47 mm/see.
帯電用部材の温度を35℃、40℃、50℃に変化させ
た。表1に種々の温度環境における初期電位、初期の画
像及び5000枚耐久後の画像について示す。比較例1
として加温手段を用いないものも同様に評価した。The temperature of the charging member was changed to 35°C, 40°C, and 50°C. Table 1 shows the initial potentials, initial images, and images after 5000 sheets in various temperature environments. Comparative example 1
Similar evaluations were made for those that did not use heating means.
表1に示すとおり、帯電用部材を35℃〜50℃に加温
使用した場合には、各環境とも初期画像も5000枚耐
久画像も良好なものが得られた。As shown in Table 1, when the charging member was heated to 35 DEG C. to 50 DEG C., good initial images and 5,000-sheet durable images were obtained in each environment.
一方、比較例1として示した加温手段を設けないものは
、低温低湿においては帯電能が悪く、帯電不良となり、
画像に砂地状の黒ポチが生じた。On the other hand, the one shown as Comparative Example 1 without the heating means had poor charging ability at low temperature and low humidity, resulting in poor charging.
Sand-like black spots appeared on the image.
23℃、60%の環境においても耐久により帯電性が悪
くなっている。Even in an environment of 23° C. and 60%, the charging property deteriorates due to durability.
比較例2として帯電用部材を60℃に加温したものを同
様に評価したが、初期より帯電用部材上及び電子写真感
光体上に、クリーナーよりすりぬけたトナーが融着した
。Comparative Example 2, in which the charging member was heated to 60° C., was similarly evaluated, but the toner that had slipped through the cleaner was fused onto the charging member and the electrophotographic photoreceptor from the beginning.
実施例4及び比較例3
実施例1で用いた帯電用部材を以下のものに代え、帯電
用部材の温度を40℃に加温して使用した以外は実施例
1と同様にして評価を行なった。Example 4 and Comparative Example 3 Evaluation was carried out in the same manner as in Example 1, except that the charging member used in Example 1 was replaced with the one below and the temperature of the charging member was heated to 40°C. Ta.
帯電用部材として、クロロプレンゴム100重量部に導
電性カーボン10重量部を溶融混練し、中心にステンレ
ス軸を通して成型したものを帯電用部材の基層として用
い、次にメトキシメチル化ナイロン10重量部をメタノ
ール90重量部に溶解し、これを基層上に浸漬塗工し、
乾燥して膜厚を100μとしたものを使用した。As a charging member, 100 parts by weight of chloroprene rubber and 10 parts by weight of conductive carbon were melt-kneaded, and a stainless steel shaft was passed through the center to form the base layer. Next, 10 parts by weight of methoxymethylated nylon was mixed with methanol. Dissolved in 90 parts by weight and dip coated on the base layer,
The film used was dried to a film thickness of 100 μm.
比較例3として、同様の帯電用部材を用いたが加温手段
を用いないものを評価した。As Comparative Example 3, a sample was evaluated in which a similar charging member was used but no heating means was used.
表
表2に示すとうり、実施例4においては、各環境とも初
期及び5000枚耐久においても良好なものが得られた
が、加温手段を設けない比較例3では低温低湿において
帯電能が悪(、帯電不良となり画像に砂地状の黒ポチが
生じた。そのレベルは比較例1と(らべても悪くなって
いる。As shown in Table 2, in Example 4, good performance was obtained in each environment both at the initial stage and in the 5,000-sheet durability test, but in Comparative Example 3, in which no heating means was provided, charging performance was poor at low temperature and low humidity. () Due to charging failure, sandy black spots appeared on the image.The level of this was worse than that of Comparative Example 1.
実施例5.6及び比較例4.5
実施例1で使用したキャノン製レーザビームプリンタ[
レーザショットLBP−A408]を改造し、プロセス
スピードを2 OrIlrn/sec、90+am/s
ecに変え、実施例4と同様に評価を行ない、それぞれ
実施例5,6とした。また、加温手段を設けないものを
それぞれ比較例4,5とした。Example 5.6 and Comparative Example 4.5 Canon laser beam printer used in Example 1 [
Lasershot LBP-A408] was modified to increase the process speed to 2 OrIrn/sec, 90+am/s
ec was used, and the same evaluation as in Example 4 was carried out, resulting in Examples 5 and 6, respectively. Further, comparative examples 4 and 5 were prepared without a heating means, respectively.
表3に示すとうり、本発明による効果はプロセススピー
ドの速い場合に一層大きいことがわかる。即ち、プロセ
ススピード90 mm/seeの場合には、比較例5に
おいて低温における帯電特性が一層悪くなり、高温高温
環境下においても本発明の範囲外の条件であると感光体
の劣化により濃度ウス、画像流れは悪くなっている。ま
た、23℃、60%環境においても耐久による帯電用部
材の劣化、帯電特性の悪化はプロセススピードの速いも
のほど悪い。一方1本発明による実施例5,6において
は、各環境とも速いプロセスス
ピードにおいても良好な画像が得られた。As shown in Table 3, it can be seen that the effect of the present invention is even greater when the process speed is high. That is, when the process speed is 90 mm/see, the charging characteristics at low temperatures in Comparative Example 5 become worse, and even in high-temperature environments, under conditions outside the range of the present invention, the photoreceptor deteriorates and the density decreases. The image flow is getting worse. Further, even in a 23° C., 60% environment, the deterioration of the charging member due to durability and the deterioration of charging characteristics are worse as the process speed is faster. On the other hand, in Examples 5 and 6 according to the present invention, good images were obtained in each environment and even at high process speeds.
[発明の効果]
以上に説明したように帯電用部材の濃度を35℃〜55
℃の範囲に維持して使用すると安定した性能を維持する
ことができる。また、帯電用部材及び感光体の劣化を防
ぐことができる。[Effect of the invention] As explained above, the concentration of the charging member is set at 35°C to 55°C.
Stable performance can be maintained if the temperature is maintained within the temperature range. Further, deterioration of the charging member and the photoreceptor can be prevented.
第1図は本発明の電子写真法に用いる装置の一例を示す
概略図である。
図中、lはレーザーショット用有機感光体、2は帯電用
部材、3は半導体レーザ露光、4は現像器、5は給紙ロ
ーラーと給紙ガイド、6は転写帯電器、7はクリーナー
、8は前露光、9は熱源である。FIG. 1 is a schematic diagram showing an example of an apparatus used in the electrophotographic method of the present invention. In the figure, l is an organic photoreceptor for laser shots, 2 is a charging member, 3 is a semiconductor laser exposure, 4 is a developing device, 5 is a paper feed roller and paper feed guide, 6 is a transfer charger, 7 is a cleaner, 8 is pre-exposure, and 9 is a heat source.
Claims (2)
印加することにより該感光体表面を帯電させる帯電プロ
セスを用いる電子写真法において、該帯電用部材の温度
を35℃〜55℃の範囲に維持して実施することを特徴
とする電子写真法。(1) In an electrophotographic method that uses a charging process in which a charging member is brought into contact with an electrophotographic photoreceptor and a voltage is applied to charge the surface of the photoreceptor, the temperature of the charging member is set at 35°C to 55°C. An electrophotographic method characterized by maintaining and performing within a range.
して帯電プロセスを実施する請求項(1)記載の電子写
真法。(2) The electrophotographic method according to claim 1, wherein the charging process is carried out at a peripheral speed of the electrophotographic photoreceptor of 40 mm/sec or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10661390A JPH046567A (en) | 1990-04-24 | 1990-04-24 | Electrophotographic method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10661390A JPH046567A (en) | 1990-04-24 | 1990-04-24 | Electrophotographic method |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH046567A true JPH046567A (en) | 1992-01-10 |
Family
ID=14437974
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10661390A Pending JPH046567A (en) | 1990-04-24 | 1990-04-24 | Electrophotographic method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH046567A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0652492A1 (en) * | 1993-11-09 | 1995-05-10 | Ricoh Company, Ltd | Image forming apparatus with a contact member contacting an image carrier |
US6449449B1 (en) | 1999-07-19 | 2002-09-10 | Ricoh Company, Ltd. | Apparatus for image forming and charging capable of effectively maintaining a charge potential |
-
1990
- 1990-04-24 JP JP10661390A patent/JPH046567A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0652492A1 (en) * | 1993-11-09 | 1995-05-10 | Ricoh Company, Ltd | Image forming apparatus with a contact member contacting an image carrier |
US6449449B1 (en) | 1999-07-19 | 2002-09-10 | Ricoh Company, Ltd. | Apparatus for image forming and charging capable of effectively maintaining a charge potential |
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