JPH04306673A - Member for electrification - Google Patents
Member for electrificationInfo
- Publication number
- JPH04306673A JPH04306673A JP9604691A JP9604691A JPH04306673A JP H04306673 A JPH04306673 A JP H04306673A JP 9604691 A JP9604691 A JP 9604691A JP 9604691 A JP9604691 A JP 9604691A JP H04306673 A JPH04306673 A JP H04306673A
- Authority
- JP
- Japan
- Prior art keywords
- charging member
- resin layer
- parts
- layer
- conductive elastic
- 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.)
- Granted
Links
- 229920005989 resin Polymers 0.000 claims abstract description 80
- 239000011347 resin Substances 0.000 claims abstract description 80
- 229920000049 Carbon (fiber) Polymers 0.000 claims abstract description 25
- 239000004917 carbon fiber Substances 0.000 claims abstract description 25
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000010410 layer Substances 0.000 claims description 138
- 239000011241 protective layer Substances 0.000 claims description 9
- 239000000463 material Substances 0.000 abstract description 16
- 239000011230 binding agent Substances 0.000 abstract description 14
- 239000002689 soil Substances 0.000 abstract 2
- 230000001419 dependent effect Effects 0.000 abstract 1
- 239000013013 elastic material Substances 0.000 abstract 1
- 108091008695 photoreceptors Proteins 0.000 description 54
- 238000012546 transfer Methods 0.000 description 51
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 42
- 230000000052 comparative effect Effects 0.000 description 30
- 230000003068 static effect Effects 0.000 description 27
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 26
- 238000001035 drying Methods 0.000 description 23
- 238000000034 method Methods 0.000 description 23
- 238000003618 dip coating Methods 0.000 description 20
- 230000008030 elimination Effects 0.000 description 16
- 238000003379 elimination reaction Methods 0.000 description 16
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 14
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 13
- 239000000126 substance Substances 0.000 description 13
- 238000004140 cleaning Methods 0.000 description 10
- 239000000049 pigment Substances 0.000 description 10
- 239000004687 Nylon copolymer Substances 0.000 description 9
- 229910052782 aluminium Inorganic materials 0.000 description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 8
- 230000007547 defect Effects 0.000 description 8
- 238000005259 measurement Methods 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 238000011161 development Methods 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 230000005611 electricity Effects 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 229920000515 polycarbonate Polymers 0.000 description 6
- 239000004417 polycarbonate Substances 0.000 description 6
- 230000015556 catabolic process Effects 0.000 description 5
- -1 hydrazone compounds Chemical class 0.000 description 5
- 229920002635 polyurethane Polymers 0.000 description 5
- 239000004814 polyurethane Substances 0.000 description 5
- 239000010935 stainless steel Substances 0.000 description 5
- 229910001220 stainless steel Inorganic materials 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
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000004952 Polyamide Substances 0.000 description 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 230000006870 function Effects 0.000 description 4
- 229920002647 polyamide Polymers 0.000 description 4
- 229920001230 polyarylate Polymers 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- 229920002292 Nylon 6 Polymers 0.000 description 3
- 239000002033 PVDF binder Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 230000001050 lubricating effect Effects 0.000 description 3
- 238000005667 methoxymethylation reaction Methods 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 229920006287 phenoxy resin Polymers 0.000 description 3
- 239000013034 phenoxy resin Substances 0.000 description 3
- 229920002382 photo conductive polymer Polymers 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920001084 poly(chloroprene) Polymers 0.000 description 3
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 3
- 239000004810 polytetrafluoroethylene Substances 0.000 description 3
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 241000519995 Stachys sylvatica Species 0.000 description 2
- 239000005018 casein Substances 0.000 description 2
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical group 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 2
- 235000021240 caseins Nutrition 0.000 description 2
- 239000002800 charge carrier Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000113 methacrylic resin Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 238000001771 vacuum deposition Methods 0.000 description 2
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- 229920006370 Kynar Polymers 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- AZWHFTKIBIQKCA-UHFFFAOYSA-N [Sn+2]=O.[O-2].[In+3] Chemical compound [Sn+2]=O.[O-2].[In+3] AZWHFTKIBIQKCA-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy 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
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 238000009125 cardiac resynchronization therapy Methods 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000007770 graphite material Substances 0.000 description 1
- 150000008282 halocarbons 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
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002916 oxazoles Chemical class 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- 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 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 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
- INAAIJLSXJJHOZ-UHFFFAOYSA-N pibenzimol Chemical compound C1CN(C)CCN1C1=CC=C(N=C(N2)C=3C=C4NC(=NC4=CC=3)C=3C=CC(O)=CC=3)C2=C1 INAAIJLSXJJHOZ-UHFFFAOYSA-N 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920001197 polyacetylene Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 229920000123 polythiophene Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002717 polyvinylpyridine Polymers 0.000 description 1
- 150000003219 pyrazolines Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010186 staining Methods 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
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Landscapes
- Discharging, Photosensitive Material Shape In Electrophotography (AREA)
- Electrostatic Charge, Transfer And Separation In Electrography (AREA)
- Inorganic Fibers (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は帯電用部材に関し、特に
は電子写真法における一次帯電用、転写帯電用、除電帯
電用に用いられる帯電用部材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a charging member, and more particularly to a charging member used for primary charging, transfer charging, and static elimination charging in electrophotography.
【0002】0002
【従来の技術】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(DC5〜8kV)を印加して発生するコロ
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
、ワイヤーの汚れ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。一方、電力的にも、感
光体に向う電流は、全電流の5〜30%にすぎず、多く
はシールド板に流れるため、帯電手段としては効果の悪
いものであった。2. Description of the Related Art Conventionally, the charging process in an electrophotographic process using an electrophotographic photoreceptor has mostly been performed by applying a high voltage (DC 5 to 8 kV) to a metal wire and using corona generated. However, with this method, when corona occurs, the surface of the photoreceptor is altered by corona products such as ozone and NOx, causing image blurring and deterioration, and wire dirt affects image quality, resulting in white spots and black lines in the image. There were problems such as the occurrence of On the other hand, in terms of electric power, the current flowing to the photoreceptor is only 5 to 30% of the total current, and most of it flows to the shield plate, making it ineffective as a charging means.
【0003】こうした欠点を補うために、直接帯電させ
る方法が研究され、多数提案されている(たとえば特開
昭57−178267号公報、特開昭56−10435
1号公報、特開昭58−40566号公報、特開昭58
−139156号公報、特開昭58−150975号公
報等)。In order to compensate for these drawbacks, direct charging methods have been researched and many proposals have been made (for example, Japanese Patent Laid-Open Nos. 57-178267 and 1982-10435).
1 Publication, JP-A-58-40566, JP-A-58
-139156, JP-A-58-150975, etc.).
【0004】0004
【発明が解決しようとする課題】しかしながら上記のよ
うな直接帯電法によって感光体を帯電処理しても、実際
には感光体の表面全体にわたる均一な帯電はなされず、
斑点状の帯電ムラが生じるのを避けられない。このよう
な斑点状帯電ムラのある感光体に光像露光およびこれに
つづくプロセスを適用した場合、得られる出力画像は、
反転現像方式では、斑点状帯電ムラに対応した斑点状の
黒点画像、また正現像方式では斑点状の白点画像となり
、高品位な画像は得られない。[Problems to be Solved by the Invention] However, even if the photoreceptor is charged by the above-mentioned direct charging method, uniform charging is not achieved over the entire surface of the photoreceptor;
Spot-like charging unevenness cannot be avoided. When photoimage exposure and subsequent processes are applied to a photoconductor with such spotty charging unevenness, the resulting output image is
In the reversal development method, a speckled black dot image corresponding to spotty charging unevenness is produced, and in the normal development method, a speckled white dot image is produced, making it impossible to obtain a high-quality image.
【0005】また直接帯電法は、多数の提案があるにも
かかわらず、市場実績が全くない。その理由として、帯
電の不均一性、および電圧の直接印加による感光体の放
電による絶縁破壊の発生などが挙げられる。放電による
絶縁破壊で生じた破壊点は、たとえば円筒状感光体の場
合、帯電電荷がその破壊点に向かって軸方向に流れ、帯
電しなくなる欠点を生じる。[0005]Also, although there are many proposals for the direct charging method, there is no market experience at all. Reasons for this include non-uniform charging and occurrence of dielectric breakdown due to discharge of the photoreceptor due to direct application of voltage. For example, in the case of a cylindrical photoreceptor, a breakdown point caused by dielectric breakdown due to discharge causes the charged charge to flow in the axial direction toward the breakdown point, resulting in a disadvantage that the photoconductor is no longer charged.
【0006】この絶縁破壊を防止するために、表面に樹
脂層を設けた帯電用部材も報告されている(たとえば特
開平1−205180号および特開平1−211779
号公報)。しかしこれらの材料も低温低湿下での抵抗値
の変動が大きく、帯電性が不安定であったり、また有機
感光体と接触させて用いると、有機感光体と帯電用部材
との表面で樹脂同士が相溶化し、互いに固着してしまう
などの欠陥をもっていた。また帯電用部材表面にゴミ、
チリの付着が多く、これが耐久性の向上しない原因とな
っている。またクリーニング不良のトナーが帯電用部材
に付着して積み重なり、フィルミングの現象を発生して
帯電性能を低下させていた。トナーが帯電用部材表面を
滑り易くする方法として、樹脂粉体を使用することも検
討されている(特開平1−66673号公報)が、樹脂
の絶縁性のために、樹脂粉体そのものが帯電性能を劣化
させることになっていた。[0006] In order to prevent this dielectric breakdown, charging members having a resin layer provided on the surface have also been reported (for example, JP-A-1-205180 and JP-A-1-211779).
Publication No.). However, these materials also have large fluctuations in resistance at low temperatures and low humidity, and are unstable in their charging properties.Also, when used in contact with an organic photoreceptor, the resins may bond with each other on the surface of the organic photoreceptor and the charging member. They had defects such as becoming compatibilized and sticking to each other. In addition, there may be dust on the surface of the charging member.
There is a lot of dust attached, which is the reason why the durability does not improve. In addition, toner that has been poorly cleaned adheres to the charging member and accumulates, causing a filming phenomenon and deteriorating charging performance. The use of resin powder has been considered as a method for making it easier for toner to slide on the surface of the charging member (Japanese Patent Laid-Open No. 1-66673), but due to the insulating properties of the resin, the resin powder itself is not charged. It was supposed to degrade performance.
【0007】本発明は上述のような従来の帯電用部材が
有している課題を解決するためになされたもので、不均
一な帯電による斑点状カブリのない高品位の画像を安定
して供給でき、しかも耐久性にすぐれた帯電用部材を提
供することを目的とする。The present invention has been made to solve the above-mentioned problems with conventional charging members, and is capable of stably supplying high-quality images without spotty fog caused by non-uniform charging. To provide a charging member that can be used for charging and has excellent durability.
【0008】[0008]
【課題を解決するための手段】本発明は、導電性支持体
およびその上に設けられた導電性弾性体からなる帯電用
部材において、導電性弾性体の上に、炭素繊維を含有す
る樹脂層を設けたことを特徴とする。[Means for Solving the Problems] The present invention provides a charging member comprising a conductive support and a conductive elastic body provided thereon, in which a resin layer containing carbon fiber is provided on the conductive elastic body. It is characterized by having the following.
【0009】以下に本発明について図面を参照してさら
に詳しく説明する。The present invention will be explained in more detail below with reference to the drawings.
【0010】本発明の帯電用部材は、たとえば図1に示
すようなローラ状のもので、軸の形態をなす導電性支持
体1およびその周囲に設けられた導電性弾性層2を備え
、この導電性弾性層2上に樹脂層3が設けられている。
そしてこの樹脂層3は、バインダー樹脂に、炭素繊維を
混入した材料で構成される。The charging member of the present invention is, for example, roller-shaped as shown in FIG. 1, and includes a conductive support 1 in the form of a shaft and a conductive elastic layer 2 provided around the support. A resin layer 3 is provided on the conductive elastic layer 2. The resin layer 3 is made of a material in which carbon fibers are mixed into a binder resin.
【0011】すなわち本発明の帯電用部材は、導電性弾
性層2上に炭素繊維を混入した樹脂層3を有するので、
電子写真感光体との付着性が少なく、かつ柔軟性もある
ので、高画質の画像を与え、トナーの汚れも少なく、低
温低湿下でも樹脂層の体積抵抗の変動が少なく、かつ耐
久性のある帯電用部材として有利に使用することができ
る。That is, since the charging member of the present invention has the resin layer 3 mixed with carbon fiber on the conductive elastic layer 2,
It has low adhesion to the electrophotographic photoreceptor and is flexible, so it provides high-quality images, less toner stains, less variation in volume resistivity of the resin layer even under low temperature and low humidity, and is durable. It can be advantageously used as a charging member.
【0012】これに対して従来の帯電用部材は、表面が
ゴムあるいはポリウレタンで構成されていたため、電子
写真感光体と接触させたままでおくと、感光体と固着し
たり、表面が硬い場合には感光体にしわを発生させたり
して、画像欠陥を生じていた。本発明によれば、このよ
うな欠点はすべて解消される。In contrast, conventional charging members have surfaces made of rubber or polyurethane, so if they are left in contact with the electrophotographic photoreceptor, they may stick to the photoreceptor, or if the surface is hard, This caused wrinkles on the photoreceptor, resulting in image defects. According to the invention, all such drawbacks are eliminated.
【0013】本発明の帯電用部材において、樹脂層3の
厚さは、炭素繊維の混入量などの条件によっても異なる
が、5〜500μm、とくに20〜200μmの範囲が
好ましい。In the charging member of the present invention, the thickness of the resin layer 3 is preferably in the range of 5 to 500 μm, particularly 20 to 200 μm, although it varies depending on conditions such as the amount of carbon fiber mixed.
【0014】バインダー樹脂としては、ポリアミド、ポ
リウレタン、ポリメチルメタクリレートまたはポリブチ
ルメタクリレートのようなアクリル樹脂、ポリビニルブ
チラール、ポリビニルアセタール、ポリアリレート、ポ
リカーボネート、フェノキシ樹脂、ポリ酢酸ビニル、ポ
リビニルピリジン等を挙げることができる。Examples of the binder resin include polyamide, polyurethane, acrylic resin such as polymethyl methacrylate or polybutyl methacrylate, polyvinyl butyral, polyvinyl acetal, polyarylate, polycarbonate, phenoxy resin, polyvinyl acetate, polyvinylpyridine, and the like. can.
【0015】このバインダー樹脂に混入させる炭素繊維
は、ポリアクリロニトリル、レーヨン、ピッチ類の3種
の原料から製造されている。強度の点から低弾性率品(
LM)、中強度品(A)、高強度品(HS)、高弾性率
品(HM)、超高弾性率品(UHM)に分類される。The carbon fibers to be mixed into this binder resin are manufactured from three types of raw materials: polyacrylonitrile, rayon, and pitch. From the viewpoint of strength, low elastic modulus products (
LM), medium strength products (A), high strength products (HS), high modulus products (HM), and ultra high modulus products (UHM).
【0016】本発明に用いる炭素繊維はいずれの強度の
ものでも用いられる。特にはLMタイプでグラファイト
質のものが好ましい。Carbon fibers of any strength can be used in the present invention. In particular, LM type graphite materials are preferred.
【0017】本発明に用いる炭素繊維の繊維径は10μ
以下、繊維長は20μから10000μまでのものが用
いられる。[0017] The fiber diameter of the carbon fiber used in the present invention is 10μ.
Hereinafter, the fiber length used is from 20μ to 10,000μ.
【0018】樹脂層3は、106〜1012Ω・cmの
範囲の体積抵抗率を有していることが好ましい。また特
願昭第62−230334号に記載されているように、
樹脂層3の体積抵抗率は、これに接している弾性層2の
それよりも大きいことが好ましい。弾性層2の体積抵抗
率としては、100〜1011Ω・cm、とくに102
〜1010Ω・cmの範囲が好ましい。弾性層2として
は、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、カー
ボンまたは金属で導電性処理したゴムまたは絶縁性樹脂
、あるいはポリカーボネート、ポリエステル等の絶縁性
樹脂またはゴムの表面を金属などの導電性物質によって
ラミネートコートしたもの、等を用いることができる。
またこの弾性層2は、個々の機能を各層に分担させた多
層構成であってもよい。Preferably, the resin layer 3 has a volume resistivity in the range of 10 6 to 10 12 Ω·cm. Also, as stated in Japanese Patent Application No. 62-230334,
The volume resistivity of the resin layer 3 is preferably larger than that of the elastic layer 2 that is in contact with it. The volume resistivity of the elastic layer 2 is 100 to 1011 Ω·cm, particularly 102
A range of 1010 Ω·cm is preferable. As the elastic layer 2, metals such as aluminum, iron, copper, polyacetylene,
Conductive polymers such as polypyrrole and polythiophene, rubber or insulating resin treated with conductivity with carbon or metal, or insulating resin or rubber such as polycarbonate or polyester whose surface is laminated and coated with a conductive substance such as metal; etc. can be used. Further, the elastic layer 2 may have a multilayer structure in which each layer has a separate function.
【0019】導電性基体1の材料としては、鉄、銅、ス
テンレスなどを用いることができる。As the material of the conductive substrate 1, iron, copper, stainless steel, etc. can be used.
【0020】さらに図2に示すように、帯電用部材は、
樹脂層3を保護するための保護層4を最外層に有してい
てもよい。この保護層4は、その内部に、導電性を制御
するための導電粒子、あるいは表面粗さを制御するため
の不溶性の樹脂粒子などの粒子5を混入したものでもよ
い。また図3に示すように、平板状の導電性支持体1に
取り付けた導電性弾性層2を備え、この導電性弾性層2
上に樹脂層3を設けた構造のものでもよい。そしてこの
樹脂層3は、バインダー樹脂に、炭素繊維を混入した材
料で構成される。Furthermore, as shown in FIG. 2, the charging member is
A protective layer 4 for protecting the resin layer 3 may be provided as the outermost layer. This protective layer 4 may have particles 5 mixed therein, such as conductive particles for controlling conductivity or insoluble resin particles for controlling surface roughness. Further, as shown in FIG. 3, a conductive elastic layer 2 attached to a flat conductive support 1 is provided.
It may also have a structure in which a resin layer 3 is provided thereon. The resin layer 3 is made of a material in which carbon fibers are mixed into a binder resin.
【0021】帯電用部材の形状は、ローラー形状やブレ
ード形状などいずれでもよいが、均一帯電の点ではロー
ラー形状が好ましい。The charging member may have any shape such as a roller shape or a blade shape, but a roller shape is preferable in terms of uniform charging.
【0022】電子写真感光体は、導電性支持体上に感光
層を設けた構成を基本としている。導電性支持体として
は、支持体自体が導電性をもつもの、たとえばアルミニ
ウム、アルミニウム合金、ステンレス、クロム、チタン
などを用いることができ、そのほかにアルミニウム、ア
ルミニウム合金、酸化インジウム−酸化錫合金などを真
空蒸着によって被膜形成された層を有する前記導電性支
持体やプラスチック、導電性粒子(たとえばカーボンブ
ラック、酸化錫粒子など)を適当なバインダーとともに
プラスチックや紙に含浸した支持体、導電性バインダー
を有するプラスチックなどを用いることができる。The electrophotographic photoreceptor basically has a structure in which a photosensitive layer is provided on a conductive support. As the conductive support, materials whose support itself is conductive can be used, such as aluminum, aluminum alloy, stainless steel, chromium, titanium, etc. In addition, aluminum, aluminum alloy, indium oxide-tin oxide alloy, etc. can be used. The conductive support or plastic has a layer formed by vacuum deposition, a support in which plastic or paper is impregnated with conductive particles (e.g. carbon black, tin oxide particles, etc.) together with a suitable binder, or a conductive binder. Plastic or the like can be used.
【0023】導電性支持体と感光層の中間に、バリヤー
機能と接着機能をもつ下引層を設けることもできる。下
引層はカゼイン、ポリビニルアルコール、ニトロセルロ
ース、エチレン−アクリル酸コポリマー、ポリアミド、
ポリウレタン、ゼラチン、酸化アルミニウムなどによっ
て形成できる。下引層の膜厚は5μm以下、好ましくは
0.5〜3μmが適当である。下引層はその機能を発揮
するためには、107Ω・cm 以上であることが好
ましい。A subbing layer having barrier and adhesive functions can also be provided between the conductive support and the photosensitive layer. The subbing layer is casein, polyvinyl alcohol, nitrocellulose, ethylene-acrylic acid copolymer, polyamide,
It can be formed from polyurethane, gelatin, aluminum oxide, etc. The thickness of the undercoat layer is suitably 5 μm or less, preferably 0.5 to 3 μm. In order for the undercoat layer to perform its function, it is preferable that the undercoat layer has a resistance of 10 7 Ω·cm or more.
【0024】感光層はたとえば、有機光導電体、アモル
ファスシリコン、セレンなどの光導電体を必要に応じて
結着剤と共に塗料化して塗布形成または真空蒸着によっ
てされる。また、有機光導電体を用いる場合、露光によ
り電荷担体を発生する電荷発生層と発生した電荷担体を
輸送する能力を持つ電荷輸送層との組み合わせからなる
感光層も有効に用いることができる。The photosensitive layer is formed, for example, by coating a photoconductor such as an organic photoconductor, amorphous silicon, selenium, etc. together with a binder if necessary, or by vacuum deposition. Furthermore, when using an organic photoconductor, a photosensitive layer consisting of a combination of a charge generation layer that generates charge carriers upon exposure to light and a charge transport layer that has the ability to transport the generated charge carriers can also be effectively used.
【0025】電荷発生層は、アゾ顔料、キノン顔料、キ
ノンアニン顔料、ペリレン顔料、インジゴ顔料、ビスベ
ンゾイミダゾール顔料、フタロシアニン顔料、キナクド
リン顔料などの電荷発生材料の1種類あるいは2種類以
上を蒸着するか、または適当なバインダーと共に(バイ
ンダーが無くても可)分散し塗工によって形成できる。The charge generating layer may be formed by depositing one or more charge generating materials such as azo pigments, quinone pigments, quinone anine pigments, perylene pigments, indigo pigments, bisbenzimidazole pigments, phthalocyanine pigments, and quinacridine pigments, or Alternatively, it can be formed by dispersing and coating with a suitable binder (or without a binder).
【0026】バインダーは広範囲な絶縁性樹脂または有
機光導電性ポリマーから選択できる。たとえば絶縁性樹
脂としてはポリビニルブチラール、ポリアリレート(ビ
スファノールAとフタル酸の縮重合体等)、ポリカーボ
ネート、ポリエステル、フェノキシ樹脂、アクリル樹脂
、ポリアクリルアミド樹脂、ポリアミド、セルロース系
樹脂、ウレタン樹脂、エポキシ樹脂、カゼイン、ポリビ
ニルアルコールなどをあげることができる。また、有機
光導電性ポリマーとしては、カルバゾール、ポリビニル
アントラセン、ポリビニルピレンなどが挙げられる。The binder can be selected from a wide variety of insulating resins or organic photoconductive polymers. For example, insulating resins include polyvinyl butyral, polyarylate (condensation polymer of bisphanol A and phthalic acid, etc.), polycarbonate, polyester, phenoxy resin, acrylic resin, polyacrylamide resin, polyamide, cellulose resin, urethane resin, epoxy resin, Examples include casein and polyvinyl alcohol. Further, examples of the organic photoconductive polymer include carbazole, polyvinylanthracene, polyvinylpyrene, and the like.
【0027】電荷発生層の膜厚は0.01〜15μm、
好ましくは0.05〜5μmであり、電荷発生層と結着
剤との重量比は10:1〜1:20である。The thickness of the charge generation layer is 0.01 to 15 μm,
The thickness is preferably 0.05 to 5 μm, and the weight ratio of the charge generation layer to the binder is 10:1 to 1:20.
【0028】電荷発生層用塗料に用いる溶剤は、使用す
る樹脂や電荷輸送材料の溶解性や分散安定性から選択さ
れるが、有機溶剤としてはアルコール類、スルホキシド
類、エーテル類、エステル類、脂肪族ハロゲン化炭化水
素類あるいは芳香族化合物などを用いることができる。The solvent used in the paint for the charge generation layer is selected based on the solubility and dispersion stability of the resin and charge transport material used. Examples of organic solvents include alcohols, sulfoxides, ethers, esters, and fats. Group halogenated hydrocarbons or aromatic compounds can be used.
【0029】塗工は、浸漬コーティング法、スプレーコ
ーティング法、マイヤーバーコーフィング法、ブレード
コーティング法などのコーティング法を用いて行なうこ
とができる。Coating can be carried out using a coating method such as a dip coating method, a spray coating method, a Mayer-Barkofing method, or a blade coating method.
【0030】電荷輸送層は、電荷輸送材料を成膜性のあ
る樹脂に溶解させて形成される。本発明に用いられる有
機の電荷輸送材料の例としては、ヒドラゾン系化合物、
スチルベン系化合物、ピラゾリン系化合物、オキサゾー
ル系化合物、チアゾール系化合物、トリアリールメタン
系化合物などが挙げられる。これらの電荷輸送物質は1
種または2種以上組み合わせて用いることができる。The charge transport layer is formed by dissolving a charge transport material in a film-forming resin. Examples of organic charge transport materials used in the present invention include hydrazone compounds,
Examples include stilbene compounds, pyrazoline compounds, oxazole compounds, thiazole compounds, and triarylmethane compounds. These charge transport materials are 1
It can be used in one species or in combination of two or more.
【0031】電荷輸送層に用いる結着剤の例としては、
フェノキシ樹脂、ポリアクリルアミド、ポリビニルブチ
ラール、ポリアリレート、ポリスルホン、ポリアミド、
アクリル樹脂、アクリロニトル樹脂、メタクリル樹脂、
塩化ビニル樹脂、酢酸ビニル樹脂、フェノール樹脂、エ
ポキシ樹脂、ポリエステル、アルキド樹脂、ポリカーボ
ネット、ポリウレタンあるいはこれらの樹脂の繰返し単
位のうち2つ以上を含む共重合体、たとえばスチレン−
ブタジエンコポリマー、スチレン−アクリロニトルコポ
リマー、スチレン−マレイン酸コポリマーなどを挙げる
ことができる。また、ポリ−N−ビニルカルバゾール、
ポリビニルアントラセン、ポリビニルピレンなどの有機
光導電性ポリマーからも選択できる。Examples of binders used in the charge transport layer include:
Phenoxy resin, polyacrylamide, polyvinyl butyral, polyarylate, polysulfone, polyamide,
Acrylic resin, acrylonitrile resin, methacrylic resin,
Vinyl chloride resin, vinyl acetate resin, phenolic resin, epoxy resin, polyester, alkyd resin, polycarbonate, polyurethane, or a copolymer containing two or more repeating units of these resins, such as styrene-
Examples include butadiene copolymer, styrene-acrylonite copolymer, styrene-maleic acid copolymer, and the like. Also, poly-N-vinylcarbazole,
Organic photoconductive polymers such as polyvinylanthracene and polyvinylpyrene can also be selected.
【0032】電荷輸送層の膜厚は5〜50μm、好まし
くは8〜20μmであり、電荷輸送物質と結着剤との重
量比は5:1〜1:5、好ましくは3:1〜1:3程度
である。塗工は前述のようなコーティング法を行なうこ
とができる。The thickness of the charge transport layer is 5 to 50 μm, preferably 8 to 20 μm, and the weight ratio of the charge transport material to the binder is 5:1 to 1:5, preferably 3:1 to 1: It is about 3. The coating method described above can be used for coating.
【0033】さらに、色素、顔料、有機電荷輸送物質な
どは、一般に紫外線、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潜像を形成するためには表面抵抗
率が1011Ω以上であることが望ましい。Furthermore, dyes, pigments, organic charge transport substances, etc. are generally susceptible to stains caused by ultraviolet rays, ozone, oil, etc.
Since it is sensitive to metals, a protective layer may be provided as necessary. In order to form an electrostatic latent image on this protective layer, it is desirable that the surface resistivity is 10 11 Ω or more.
【0034】感光体の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、ポリアリレート、
ポリウレタン、スチレン−ブタジエンコポリマー、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
解した駅を感光層の上に塗布、乾燥して形成できる。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 of the photoreceptor is made of polyvinyl butyral,
Polyester, polycarbonate, acrylic resin, methacrylic resin, nylon, polyimide, polyarylate,
The photosensitive layer can be formed by applying a solution of a resin such as polyurethane, styrene-butadiene copolymer, styrene-acrylic acid copolymer, styrene-acrylonitrile copolymer, etc. in a suitable organic solvent onto the photosensitive layer and drying it. At this time, the thickness of the protective layer is generally in the range of 0.05 to 20 μm. This protective layer may contain an ultraviolet absorber or the like.
【0035】本発明の帯電用部材は、たとえば図4に示
すような電子写真装置に適用することができる。この装
置は、ドラム状の電子写真感光体12の周面上に一次帯
電用部材6、像露光手段7、現像手段8、転写帯電手段
9、クリーニング手段10、および前露光手段11が配
置されている。The charging member of the present invention can be applied to an electrophotographic apparatus as shown in FIG. 4, for example. In this apparatus, a primary charging member 6, an image exposure means 7, a developing means 8, a transfer charging means 9, a cleaning means 10, and a pre-exposure means 11 are arranged on the circumferential surface of a drum-shaped electrophotographic photoreceptor 12. There is.
【0036】電子写真感光体12上に接触配置されてい
る一次帯電用部材6に、外部より電圧(たとえば200
V以上2000V以下の直流電圧とピーク間電圧400
0V以下の交流電圧を重畳した脈流電圧)を印加し、電
子写真感光体12表面を帯電させ、像露光手段7によっ
て原稿上の画像を感光体に像露光して静電潜像を形成す
る。次に現像手段8中の現像剤を感光体に付着させるこ
とにより、感光体上の静電潜像を現像(可視像化)し、
さらに感光体上の現像剤を転写帯電手段9によって紙な
どの被転写部材13に転写し、クリーニング手段10に
よって転写時に紙に転写されずに感光体上に残った現像
剤を回収する。A voltage (for example, 200
DC voltage between V and 2000V and peak-to-peak voltage 400V
A pulsating current voltage superimposed with an AC voltage of 0 V or less is applied to charge the surface of the electrophotographic photoreceptor 12, and the image on the document is exposed to the photoreceptor by the image exposure means 7 to form an electrostatic latent image. . Next, by attaching the developer in the developing means 8 to the photoreceptor, the electrostatic latent image on the photoreceptor is developed (visualized),
Further, the developer on the photoreceptor is transferred to a transfer member 13 such as paper by a transfer charging means 9, and the developer remaining on the photoreceptor without being transferred to the paper during transfer is collected by a cleaning means 10.
【0037】このような電子写真プロセスによって画像
を形成することができるが、感光体に残留電荷が残るよ
うな場合には、一次帯電を行なう前に前露光手段11に
よって感光体に光を当て残留電荷を除電したほうがよい
。Although an image can be formed by such an electrophotographic process, if residual charges remain on the photoreceptor, the photoreceptor is exposed to light by the pre-exposure means 11 before primary charging to eliminate the residual charges. It is better to eliminate the charge.
【0038】本発明の帯電用部材を転写帯電に用いる場
合、たとえば、図5に示すような電子写真装置に適用す
ることができる。この装置では、電子写真感光体12の
周面上に一次帯電用コロナ帯電器14、像露光手段7、
現像手段8、転写帯電用帯電部材15、クリーニング手
段10、前露光手段11が配置されている。When the charging member of the present invention is used for transfer charging, it can be applied to, for example, an electrophotographic apparatus as shown in FIG. In this apparatus, a corona charger 14 for primary charging, an image exposure means 7,
A developing means 8, a charging member 15 for transfer charging, a cleaning means 10, and a pre-exposure means 11 are arranged.
【0039】電子写真感光体12上に接触配置されてい
る転写帯電用帯電部材15に電圧(たとえば直流電圧4
00〜1000V)を印加し電子写真感光体上の現像剤
を紙などの被転写部材に転写することができる。A voltage (for example, a DC voltage of 4
00 to 1000 V) can be applied to transfer the developer on the electrophotographic photoreceptor to a transfer member such as paper.
【0040】本発明の帯電用部材を除電帯電に用いる場
合、たとえば、図6に示すような電子写真装置に適用す
ることができる。この装置では、電子写真感光体12の
周面上に一次帯電用コロナ帯電器14、像露光手段7、
現像手段8、転写帯電用コロナ帯電器9、クリーニング
手段10が配置されている。When the charging member of the present invention is used for static elimination charging, it can be applied to, for example, an electrophotographic apparatus as shown in FIG. In this apparatus, a corona charger 14 for primary charging, an image exposure means 7,
A developing means 8, a corona charger 9 for transfer charging, and a cleaning means 10 are arranged.
【0041】電子写真感光体12上に接触配置されてい
る除電帯電用帯電部材16に電圧(たとえば交流ピーク
間電圧500〜2000V)を印加し電子写真感光体上
の電荷を除電することができる。Electric charges on the electrophotographic photoreceptor 12 can be removed by applying a voltage (for example, AC peak-to-peak voltage of 500 to 2000 V) to the charging member 16 for charge removal that is placed in contact with the electrophotographic photoreceptor 12 .
【0042】本発明の帯電用部材は、機械的強度、化学
的安定性の点で劣化しやすい、有機光導電体を含有する
感光層を有する電子写真感光体に適用することにより、
その特性を顕著に発揮することができる。The charging member of the present invention can be applied to an electrophotographic photoreceptor having a photosensitive layer containing an organic photoconductor, which easily deteriorates in terms of mechanical strength and chemical stability.
Its characteristics can be clearly demonstrated.
【0043】本発明における感光体に接触させる帯電用
部材の設置については特定の方法に限らず、帯電用部材
は固定方式、感光体と同方向または逆方向で回転等の移
動方式いずれの方式を用いることもできる。さらに帯電
用部材に感光体上の現像剤クリーニング装置として機能
させることも可能である。[0043] The method of installing the charging member in contact with the photoreceptor in the present invention is not limited to a specific method; the charging member may be fixed or moved by rotating in the same direction or opposite direction to the photoreceptor. It can also be used. Furthermore, it is also possible to cause the charging member to function as a developer cleaning device on the photoreceptor.
【0044】本発明の直接帯電における帯電用部材への
印加電圧、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
にも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。Regarding the voltage applied to the charging member and the application method in the direct charging of the present invention, it depends on the specifications of each electrophotographic apparatus, but in addition to the method of instantly applying the desired voltage, there is also a method for protecting the photoreceptor. For this purpose, the applied voltage can be increased in stages, or in the case of applying a superimposed alternating current on direct current, the voltage can be applied in the order of direct current → alternating current or alternating current → direct current.
【0045】本発明の帯電用部材を電子写真装置の一次
帯電に用いる場合、画像出力領域の電子写真感光体に対
して直流電圧と交流電圧を重畳することが必要である。When the charging member of the present invention is used for primary charging of an electrophotographic apparatus, it is necessary to superimpose a DC voltage and an AC voltage on the electrophotographic photoreceptor in the image output area.
【0046】一次帯電を直流電圧のみで印加した場合、
均一に帯電することができない。[0046] When primary charging is applied only with DC voltage,
Unable to charge uniformly.
【0047】転写帯電に用いる場合、直流電圧のみでも
直流電圧と交流電圧を重畳しても良い。When used for transfer charging, a DC voltage alone or a DC voltage and an AC voltage may be superimposed.
【0048】除電帯電に用いる場合、交流電圧のみを印
加することが必要である。[0048] When used for static electricity removal charging, it is necessary to apply only an alternating current voltage.
【0049】また、本発明においては、画像露光、現像
およびクリーニング等のプロセスは静電写真の分野に公
知の任意の方法を採用することができ、現像剤の種類な
ど特定のものに限定されるものではない。本発明の帯電
用部材は複写器だけでなく、レザープリンターやCRT
プリンター、電子写真式製版システムなどの電子写真応
用分野にも用いることができる。Furthermore, in the present invention, processes such as image exposure, development, and cleaning can be performed using any method known in the field of electrostatic photography, and are limited to specific methods such as the type of developer. It's not a thing. The charging member of the present invention is applicable not only to copiers but also to laser printers and CRTs.
It can also be used in electrophotographic applications such as printers and electrophotographic plate making systems.
【0050】図7にドラム型感光体を用いた一般的な転
写式電子写真装置の概略構成を示した。FIG. 7 shows a schematic configuration of a general transfer type electrophotographic apparatus using a drum-type photoreceptor.
【0051】図において、101は像担持体としてのド
ラム型感光体であり軸101aを中心に矢印方向に所定
の周速度で回転駆動される。該感光体101はその回転
過程で本発明の帯電手段102によりその周面に正また
は負の所定電位の均一帯電を受け、次いで露光部103
にて不図示の像露光手段により光像露光L(スリット露
光、レーザービーム走査露光など)を受ける。これによ
り感光体周面に露光像に対応した静電潜像が順次形成さ
れていく。In the figure, reference numeral 101 denotes a drum-type photoreceptor as an image carrier, which is rotated at a predetermined circumferential speed in the direction of the arrow around a shaft 101a. The photoreceptor 101 is uniformly charged at a predetermined positive or negative potential on its circumferential surface by the charging means 102 of the present invention during its rotation process, and then charged at the exposure section 103.
At this point, a light image exposure L (slit exposure, laser beam scanning exposure, etc.) is applied by an image exposure means (not shown). As a result, electrostatic latent images corresponding to the exposed images are sequentially formed on the circumferential surface of the photoreceptor.
【0052】その静電潜像はついで現像手段104でト
ナー現像されたそのトナー現像が転写手段105により
不図示の給紙部から感光体101と転写手段105との
間に感光体101の回転と同期取りされて給送された転
写材Pの面に順次転写されていく。The electrostatic latent image is then developed with toner by the developing means 104, and the toner image is transferred by the transfer means 105 from a paper feeding section (not shown) between the photoreceptor 101 and the transfer means 105 as the photoreceptor 101 rotates. The images are sequentially transferred onto the surface of the transfer material P that is fed in synchronization.
【0053】像転写を受けた転写材Pは感光体面から分
離されて像定着手段8へ導入されて像定着を受けて複写
物(コピー)として機外へプリントアウトされる。The transfer material P that has undergone the image transfer is separated from the photoreceptor surface and introduced into the image fixing means 8, where the image is fixed and printed out as a copy to the outside of the machine.
【0054】像転写後の感光体101の表面はクリーニ
ング手段106にて転写残りトナーの除去を受けて清浄
面化されて繰り返して像形成に使用される。After the image has been transferred, the surface of the photoreceptor 101 is cleaned by a cleaning means 106 to remove residual toner and is repeatedly used for image formation.
【0055】感光体101の均一帯電手段102として
は本発明の帯電部材が使用されている。また転写装置1
05もコロナ転写手段が一般に広く使用されている。電
子写真装置として、上述の感光体や現像手段、クリーニ
ング手段などの構成要素のうち、複数のものを装置ユニ
ットとして一体に結合して構成し、このユニットを装置
本体に対して着脱自在に構成しても良い。たとえば、感
光体101とクリーニング手段106とを一体化してひ
とつの装置ユニットとし、装置本体のレールなどの案内
手段を用いて着脱自在の構成にしても良い。このとき、
上記の装置ユニットのほうに帯電手段および/または現
像手段を伴って構成しても良い。As the uniform charging means 102 for the photoreceptor 101, the charging member of the present invention is used. Also, the transfer device 1
Corona transfer means for 05 is also generally widely used. An electrophotographic apparatus is constructed by combining a plurality of components such as the above-mentioned photoreceptor, developing means, and cleaning means into an apparatus unit, and this unit is configured to be detachable from the apparatus main body. It's okay. For example, the photoreceptor 101 and the cleaning means 106 may be integrated into one device unit, and configured to be detachable using a guide means such as a rail on the main body of the device. At this time,
The above device unit may be configured with a charging means and/or a developing means.
【0056】また、光像露光Lは、電子写真装置を複写
機やプリンターとして使用する場合には、原稿からの反
射光や透過光、あるいは、原稿を読取り信号化し、この
信号によりレーザビームの走査、発光ダイオードアレイ
の駆動、または液晶シャッターアレイの駆動などにより
行なわれる。When the electrophotographic apparatus is used as a copying machine or a printer, the light image exposure L is performed using reflected light or transmitted light from a document, or by converting the document into a signal and scanning the laser beam using this signal. , driving a light emitting diode array, or driving a liquid crystal shutter array.
【0057】また、ファクシミリのプリンターとして使
用する場合には、光像露光Lは受信データをプリントす
るための露光になる。図8はこの場合の1例をブロック
図で示したものである。Furthermore, when used as a facsimile printer, the optical image exposure L is exposure for printing received data. FIG. 8 is a block diagram showing an example of this case.
【0058】コントローラ111は画像読取部110と
プリンター119を制御する。コントローラ111の全
体はCPU117により制御されている。画像読取部か
らの読取データは、送信回路113を通して相手局に送
信される。相手局から受けたデータは受信回路112を
通してプリンター119に送られる。画像メモリには所
定の画像データが記憶される。プリンタコントローラ1
18はプリンター119を制御している。114は電話
である。A controller 111 controls an image reading section 110 and a printer 119. The entire controller 111 is controlled by a CPU 117. The read data from the image reading section is transmitted to the partner station through the transmitting circuit 113. Data received from the partner station is sent to the printer 119 through the receiving circuit 112. Predetermined image data is stored in the image memory. Printer controller 1
18 controls a printer 119. 114 is a telephone.
【0059】回線115から受信された画像(回線を介
して接続されたリモート端末からの画像情報)は、受信
回路112で復調された後、CPU117は画像情報の
復号処理を行ない順次画像メモリ116に格納される。
そして、少なくとも1ページの画像がメモリ116に格
納されると、そのページの画像記録を行なう。CPU1
17は、メモリ116より1ページの画像情報を読み出
しプリンタコントローラ118に復号化された1ページ
の画像情報を送出する。プリンタコントローラ118は
、CPU117からの1ページの画像情報を受け取ると
そのページの画像情報記録を行なうべく、プリンタ11
9を制御する。After the image received from the line 115 (image information from a remote terminal connected via the line) is demodulated by the receiving circuit 112, the CPU 117 decodes the image information and sequentially stores it in the image memory 116. Stored. When the image of at least one page is stored in the memory 116, the image of that page is recorded. CPU1
17 reads one page of image information from the memory 116 and sends the decoded one page of image information to the printer controller 118. Upon receiving one page of image information from the CPU 117, the printer controller 118 controls the printer 11 to record the image information of that page.
Control 9.
【0060】尚、CPU117は、プリンタ119によ
る記録中に、次のページの受信を行なっている。Note that the CPU 117 is receiving the next page while the printer 119 is recording.
【0061】以上の様に、画像の受信と記録が行なわれ
る。[0061] As described above, images are received and recorded.
【0062】以下に本発明の実施例を示す。Examples of the present invention are shown below.
【0063】[0063]
【実施例】実施例1
導電性支持体として、肉厚0.5mmで60φ×260
mmのアルミニウムシリンダーを用意した。[Example] Example 1 As a conductive support, 60φ×260 with a wall thickness of 0.5 mm
A mm aluminum cylinder was prepared.
【0064】共重合ナイロン(商品名:CM8000、
東レ(株)製)4部およびタイプ8ナイロン(商品名:
ラッカマイド5003、大日本インキ(株)製)4部を
メタノール50部、n−ブタノール50部に溶解し、上
記支持体上に浸漬塗布して0.6μm厚の下引層を形成
した。Copolymerized nylon (product name: CM8000,
Toray Industries, Inc.) Part 4 and Type 8 Nylon (Product name:
4 parts of Laccamide 5003 (manufactured by Dainippon Ink Co., Ltd.) was dissolved in 50 parts of methanol and 50 parts of n-butanol, and the solution was dip coated onto the above support to form a 0.6 μm thick subbing layer.
【0065】下記構造式のジスアゾ顔料を10部、10 parts of a disazo pigment having the following structural formula,
【0
066】0
066]
【化1】
及びポリビニルブチラール樹脂(商品名:エスレックB
M2積水化学(株)製)10部を、シクロヘキサノン1
20部と共にサンドミル装置で10時間分散した。分散
液にメチルエチルケトン30部を加えて上記下引層上に
塗布し、0.15μ厚の電荷発生層を形成した。[Chemical formula 1] and polyvinyl butyral resin (product name: S-LEC B
10 parts of M2 (manufactured by Sekisui Chemical Co., Ltd.), 1 part of cyclohexanone
Dispersion was carried out with 20 parts in a sand mill apparatus for 10 hours. 30 parts of methyl ethyl ketone was added to the dispersion and coated on the undercoat layer to form a charge generation layer with a thickness of 0.15 μm.
【0067】重量平均分子量12万のポリカーボネート
Z樹脂(三菱瓦斯化学(株)製)10部を用意し、下記
構造式のヒドラゾン化合物10 parts of polycarbonate Z resin (manufactured by Mitsubishi Gas Chemical Co., Ltd.) having a weight average molecular weight of 120,000 was prepared, and a hydrazone compound having the following structural formula was prepared.
【0068】[0068]
【化2】
10部と共にモノクロルベンゼン80部に溶解した。こ
れを上記電荷発生層上に塗布して、16μm厚の電荷輸
送層を形成し、電子写真感光体No.1を製造した。embedded image 10 parts and 80 parts of monochlorobenzene were dissolved. This was applied onto the charge generation layer to form a charge transport layer with a thickness of 16 μm. 1 was manufactured.
【0069】次にクロロプレンゴム100重量部に導電
性カーボン5重量部を熔融混練し、中心にφ8×260
mmのステンレス軸を通してφ20×240mmになる
ように成型し、ローラー形状帯電用部材の導電性弾性層
を設けた。Next, 5 parts by weight of conductive carbon was melted and kneaded with 100 parts by weight of chloroprene rubber, and a φ8×260
It was molded into a diameter of 20 mm x 240 mm through a stainless steel shaft of mm, and a conductive elastic layer of a roller-shaped charging member was provided.
【0070】この帯電用部材の導電性弾性層の体積抵抗
を、温度22℃、湿度60%の環境で測ると3×104
Ωcmである。The volume resistivity of the conductive elastic layer of this charging member is 3×10 4 when measured in an environment with a temperature of 22° C. and a humidity of 60%.
It is Ωcm.
【0071】次にLMタイプグラファイト質炭素繊維(
径2μm,長200μm)3重量部及びナイロン共重合
体(CM8000東レ)7重量部をエタノール90重量
部に加え、ボールミルにて分散した。Next, LM type graphitic carbon fiber (
3 parts by weight (2 μm in diameter, 200 μm in length) and 7 parts by weight of a nylon copolymer (CM8000 Toray) were added to 90 parts by weight of ethanol and dispersed in a ball mill.
【0072】前記帯電用部材の導電性弾性層の上に浸漬
塗工し、乾燥後膜厚200μmの樹脂層を設け、ローラ
ー形状帯電用部材を製造した。アルミシート上に同様に
して樹脂層を設け、体積抵抗を測定した。A roller-shaped charging member was manufactured by dip coating on the conductive elastic layer of the charging member and providing a resin layer with a thickness of 200 μm after drying. A resin layer was similarly provided on an aluminum sheet, and the volume resistance was measured.
【0073】この帯電用部材を図4のように正現像方式
複写機PC−20(キヤノン製)一次コロナ帯電器の代
わりに取り付け、電子写真感光体と従動回転させ、一次
帯電電圧は直流電圧−750Vと交流ピーク間電圧15
00Vの重畳を行ない、電子写真感光体の暗電位と明電
位の電位測定及び画像を検討した。結果を表1に示した
。As shown in FIG. 4, this charging member was attached in place of the primary corona charger of a normal development type copying machine PC-20 (manufactured by Canon), and rotated in accordance with the electrophotographic photoreceptor, so that the primary charging voltage was set to a DC voltage of - 750V and AC peak-to-peak voltage 15
00V was superimposed, and the dark potential and bright potential of the electrophotographic photoreceptor were measured and the images were examined. The results are shown in Table 1.
【0074】さらに、10000枚の画像を繰り返しと
って、耐久後の電位測定及び画像を検討した。Furthermore, 10,000 images were repeatedly taken to measure the potential and examine the images after durability.
【0075】実施例2
実施例1と同様に帯電用部材の導電性弾性層を用意した
。次にLMタイプグラファイト質炭素繊維(径4μ,長
500μ)4重量部及びメトキシメチル化ナイロン−6
(メトキシメチル化率28%)6重量部をエタノール9
0重量部に加え、ボールミル分散した。Example 2 A conductive elastic layer of a charging member was prepared in the same manner as in Example 1. Next, 4 parts by weight of LM type graphitic carbon fiber (diameter 4μ, length 500μ) and methoxymethylated nylon-6
(Methoxymethylation rate 28%) 6 parts by weight to 9 parts by weight of ethanol
0 parts by weight and ball mill dispersion.
【0076】前記帯電用部材の導電性弾性層の上に浸漬
塗工し、乾燥後膜厚200μmの樹脂層を設け、ローラ
ー形状帯電用部材を製造した。これを実施例1と同様に
評価し、表1に示した。A roller-shaped charging member was manufactured by dip coating on the conductive elastic layer of the charging member and providing a resin layer with a thickness of 200 μm after drying. This was evaluated in the same manner as in Example 1 and is shown in Table 1.
【0077】実施例3
実施例1と同様に帯電用部材の導電性弾性層を用意した
。次にHSタイプ炭素繊維(径4μm,長1000μm
)2重量部及びポリビニルブチラール(BX−1積水化
学)8重量部をエタノール90重量部に加え、ボールミ
ル分散した。Example 3 A conductive elastic layer of a charging member was prepared in the same manner as in Example 1. Next, HS type carbon fiber (diameter 4 μm, length 1000 μm
) and 8 parts by weight of polyvinyl butyral (BX-1 Sekisui Chemical) were added to 90 parts by weight of ethanol and dispersed in a ball mill.
【0078】前記帯電用部材の導電性弾性層の上に浸漬
塗工し、乾燥後膜厚200μmの樹脂層を設け、ローラ
ー形状帯電用部材を製造した。これを実施例1と同様に
評価し、表1に示した。A roller-shaped charging member was manufactured by dip coating on the conductive elastic layer of the charging member and providing a resin layer with a thickness of 200 μm after drying. This was evaluated in the same manner as in Example 1 and is shown in Table 1.
【0079】実施例4
実施例1と同様に帯電用部材の導電性弾性層を用意した
。次にHMタイプ炭素繊維(径8μm,長5000μm
)5重量部及び塩ビ、酢ビ共重合体(VMCH、UCC
製)5重量部をメチルエチルケトン90重量部に加えボ
ールミル分散した。Example 4 A conductive elastic layer of a charging member was prepared in the same manner as in Example 1. Next, HM type carbon fiber (diameter 8 μm, length 5000 μm
) 5 parts by weight and vinyl chloride, vinyl acetate copolymer (VMCH, UCC
5 parts by weight of methyl ethyl ketone were added to 90 parts by weight of methyl ethyl ketone and dispersed in a ball mill.
【0080】前記帯電用部材の導電性弾性層の上に浸漬
塗工し、乾燥後膜厚200μmの樹脂層を設け、ローラ
ー形状帯電用部材を製造した。これを実施例1と同様に
評価し、表1に示した。A roller-shaped charging member was manufactured by dip coating on the conductive elastic layer of the charging member and providing a resin layer with a thickness of 200 μm after drying. This was evaluated in the same manner as in Example 1 and is shown in Table 1.
【0081】比較例1
実施例1と同様に帯電用部材の導電性弾性層を用意した
。次に導電性カーボン(コンダクテックスC−900コ
ロンビアンカーボン製)3重量部及びナイロン共重合体
(CM8000東レ)7重量部をエタノール90重量部
に加え、ボールミル分散した。Comparative Example 1 A conductive elastic layer of a charging member was prepared in the same manner as in Example 1. Next, 3 parts by weight of conductive carbon (Conductex C-900 manufactured by Columbia Carbon) and 7 parts by weight of nylon copolymer (CM8000 manufactured by Toray) were added to 90 parts by weight of ethanol and dispersed in a ball mill.
【0082】前記帯電用部材の導電性弾性層の上に浸漬
塗工し、乾燥後膜厚200μmの樹脂層を設け、ローラ
ー形状帯電用部材を製造した。これを実施例1と同様に
初期の電位測定及び画像を評価し、表1に示した。さら
に5000枚の画像を繰り返しとって耐久後の電位測定
及び画像を検討した。A roller-shaped charging member was manufactured by dip coating on the conductive elastic layer of the charging member and providing a resin layer with a thickness of 200 μm after drying. The initial potential measurement and images were evaluated in the same manner as in Example 1, and the results are shown in Table 1. Furthermore, 5,000 images were repeatedly taken, and the potential measurement and images after durability were examined.
【0083】比較例2
実施例1と同様に帯電用部材の導電性弾性層を用意した
。次にポリテトラフルオロエチレン微粉末(ルブロンL
−2ダイキン製)2重量部及びナイロン共重合体(CM
8000東レ製)8重量部をエタノール90重量部に加
えボールミル分散した。Comparative Example 2 A conductive elastic layer of a charging member was prepared in the same manner as in Example 1. Next, polytetrafluoroethylene fine powder (Luburon L)
-2 Daikin) 2 parts by weight and nylon copolymer (CM
8000 manufactured by Toray Industries) was added to 90 parts by weight of ethanol and dispersed in a ball mill.
【0084】前記帯電用部材の導電性弾性層の上に浸漬
塗工し、乾燥後膜厚200μmの樹脂層を設け、ローラ
ー形状帯電用部材を製造した。これを比較例1と同様に
評価し、表1に示した。A roller-shaped charging member was manufactured by dip coating on the conductive elastic layer of the charging member and providing a resin layer with a thickness of 200 μm after drying. This was evaluated in the same manner as Comparative Example 1 and shown in Table 1.
【0085】比較例3
実施例1と同様に帯電用部材の導電性弾性層を用意した
。次にポリフッ化ビニリデン微粉末(カイナー巴工業)
2重量部及びポリビニルブチラール(エスレックBX−
1積水化学製)8重量部をメチルエチルケトン90重量
部に加え、ボールミル分散した。Comparative Example 3 A conductive elastic layer of a charging member was prepared in the same manner as in Example 1. Next, polyvinylidene fluoride fine powder (Kyner Tomoe Industries)
2 parts by weight and polyvinyl butyral (S-LEC BX-
1 (manufactured by Sekisui Chemical) was added to 90 parts by weight of methyl ethyl ketone and dispersed in a ball mill.
【0086】前記帯電用部材の導電性弾性層の上に浸漬
塗工し、乾燥後膜厚200μmの樹脂層を設け、ローラ
ー形状帯電用部材を製造した。これを比較例1と同様に
評価し、表1に示した。A roller-shaped charging member was manufactured by dip coating on the conductive elastic layer of the charging member and providing a resin layer with a thickness of 200 μm after drying. This was evaluated in the same manner as Comparative Example 1 and shown in Table 1.
【0087】比較例4
実施例1と同様に帯電用部材の導電性弾性層を用意した
。次にポリビニルブチラール(エスレックBX−1積水
化学)10重量部をメチルエチルケトン90重量部に溶
解し、前記帯電用部材の導電性弾性層の上に浸漬塗工し
、乾燥後膜厚200μmの樹脂層を設け、ローラー形状
帯電用部材を製造とした。これを比較例1と同様に評価
し、表1に示した。Comparative Example 4 A conductive elastic layer of a charging member was prepared in the same manner as in Example 1. Next, 10 parts by weight of polyvinyl butyral (S-LEC BX-1 Sekisui Chemical) was dissolved in 90 parts by weight of methyl ethyl ketone, and the solution was dip coated onto the conductive elastic layer of the charging member, and after drying, a resin layer with a thickness of 200 μm was formed. and manufactured a roller-shaped charging member. This was evaluated in the same manner as Comparative Example 1 and shown in Table 1.
【0088】実施例1、2、3、4と比較例1、4を比
較してわかるように本発明では耐久時の帯電部材のトナ
ー汚れによるフィルミングを防止し、画像欠陥の発生を
防止できる。As can be seen by comparing Examples 1, 2, 3, and 4 with Comparative Examples 1 and 4, the present invention can prevent filming due to toner stains on the charging member during durability, and can prevent image defects from occurring. .
【0089】また、実施例1、2、3、4と比較例4を
比較してわかるように帯電部材と感光体との融着を防止
し、横スジ欠陥画像の発生を抑えることができる。Furthermore, as can be seen by comparing Examples 1, 2, 3, and 4 with Comparative Example 4, it is possible to prevent fusion between the charging member and the photoreceptor, and to suppress the occurrence of horizontal stripe defect images.
【0090】比較例2、3では樹脂の潤滑性添加剤を用
いており、耐久時に帯電性能が劣化し、濃度低下を発生
している。次に転写帯電器としての特性を調べた。In Comparative Examples 2 and 3, a resin lubricating additive was used, and the charging performance deteriorated during durability, resulting in a decrease in concentration. Next, we investigated its characteristics as a transfer charger.
【0091】実施例5
実施例1と同様にして感光体を作製した。次にクロロプ
レンゴム100重量部に導電性カーボン5重量部を熔融
混練し、中心にφ8×260mmのステンレス軸を通し
てφ30×240mmになるように成型し、ローラー形
状帯電用部材の導電性弾性層を設けた。Example 5 A photoreceptor was produced in the same manner as in Example 1. Next, 100 parts by weight of chloroprene rubber was melted and kneaded with 5 parts by weight of conductive carbon, passed through a stainless steel shaft of 8 x 260 mm in the center, and formed into a 30 x 240 mm diameter, and a conductive elastic layer of a roller-shaped charging member was provided. Ta.
【0092】この転写帯電用部材の体積抵抗を温度22
℃、湿度60%の環境で測ると4×104Ωcmである
。The volume resistance of this transfer charging member was determined at a temperature of 22
When measured in an environment of ℃ and 60% humidity, it is 4 x 104 Ωcm.
【0093】次にLMタイプグラファイト質炭素繊維(
径2μm,長200μm)4重量部及びナイロン共重合
体(CM8000東レ)6重量部をエタノール90重量
部に溶解し、前記転写帯電用部材の導電性弾性層の上に
浸漬塗工し、乾燥後膜厚100μmの樹脂層を設け、ロ
ーラー形状転写帯電用部材を製造した。アルミシート上
に同様に樹脂層を設け、体積抵抗を測定した。Next, LM type graphitic carbon fiber (
2 μm in diameter, 200 μm in length) and 6 parts by weight of nylon copolymer (CM8000 Toray) were dissolved in 90 parts by weight of ethanol, dip coated onto the conductive elastic layer of the transfer charging member, and after drying. A resin layer with a thickness of 100 μm was provided to produce a roller shape transfer charging member. A resin layer was similarly provided on the aluminum sheet, and the volume resistance was measured.
【0094】この転写帯電用部材を図5のように正現像
方式複写機PC−20(キャノン製)の転写コロナ帯電
器の代わりに取り付け、転写帯電は直流−500Vを印
加し、画像及び転写帯電部材の状態を検討した。結果を
表2に示した。さらに、10000枚の画像を繰り返し
とって、耐久後の電位測定及び画像を検討した。This transfer charging member was installed in place of the transfer corona charger of the normal development type copying machine PC-20 (manufactured by Canon) as shown in FIG. The condition of the parts was examined. The results are shown in Table 2. Furthermore, 10,000 images were repeatedly taken, and the potential measurements and images after durability were examined.
【0095】実施例6
実施例5と同様に転写帯電用部材の導電性弾性層を用意
した。次にLMタイプグラファイト質炭素繊維(径4μ
m,長500μm)5重量部及びメトキシメチル化ナイ
ロン−6(メトキシメチル化率28%)5重量部をエタ
ノール90重量部に加えボールミル分散した。Example 6 A conductive elastic layer of a transfer charging member was prepared in the same manner as in Example 5. Next, LM type graphitic carbon fiber (diameter 4μ
500 μm in length) and 5 parts by weight of methoxymethylated nylon-6 (methoxymethylation rate 28%) were added to 90 parts by weight of ethanol and dispersed in a ball mill.
【0096】前記転写帯電用部材の導電性弾性層の上に
浸漬塗工し、乾燥後膜厚100μmの樹脂層を設け、ロ
ーラー形状転写帯電用部材を製造した。これを実施例5
と同様に評価し、表2に示した。A roller-shaped transfer charging member was manufactured by dip coating on the conductive elastic layer of the transfer charging member and providing a resin layer with a thickness of 100 μm after drying. Example 5
The results are shown in Table 2.
【0097】実施例7
実施例5と同様に転写帯電用部材の導電性弾性層を用意
した。次にHSタイプ炭素繊維(径4μm,長1000
μm)3重量部及びポリビニルブチラール(BX−1積
水化学)7重量部をメチルエチルケトン90重量部に加
え、ボールミル分散した。Example 7 A conductive elastic layer of a transfer charging member was prepared in the same manner as in Example 5. Next, HS type carbon fiber (diameter 4 μm, length 1000
3 parts by weight of polyvinyl butyral (BX-1 Sekisui Chemical) were added to 90 parts by weight of methyl ethyl ketone and dispersed in a ball mill.
【0098】前記転写帯電用部材の導電性弾性層の上に
浸漬塗工し、乾燥後膜厚100μmの樹脂層を設け、ロ
ーラー形状転写帯電用部材を製造した。これを実施例5
と同様に評価し、表2に示した。A roller-shaped transfer charging member was manufactured by dip coating on the conductive elastic layer of the transfer charging member and providing a resin layer with a thickness of 100 μm after drying. Example 5
The results are shown in Table 2.
【0099】実施例8
実施例5と同様に転写帯電用部材の導電性弾性層を用意
した。次にHMタイプ炭素繊維(径8μm,長500μ
m)5重量部及び塩ビ、酢ビ共重合体(VMCH、UC
C)5重量部をメチルエチルケトン90重量部に加えボ
ールミル分散した。Example 8 A conductive elastic layer of a transfer charging member was prepared in the same manner as in Example 5. Next, HM type carbon fiber (diameter 8 μm, length 500 μm
m) 5 parts by weight and vinyl chloride, vinyl acetate copolymer (VMCH, UC
C) 5 parts by weight were added to 90 parts by weight of methyl ethyl ketone and dispersed in a ball mill.
【0100】前記転写帯電用部材の導電性弾性層の上に
浸漬塗工し、乾燥後膜厚100μmの樹脂層を設け、ロ
ーラー形状転写帯電用部材を製造した。これを実施例5
と同様に評価し、表2に示した。A roller-shaped transfer charging member was manufactured by dip coating on the conductive elastic layer of the transfer charging member and providing a resin layer with a thickness of 100 μm after drying. Example 5
The results are shown in Table 2.
【0101】比較例5
実施例5と同様に転写帯電用部材の導電性弾性層を用意
した。次に導電性カーボン(コンダクテックスC−90
0コロンビアンカーボン製)3重量部及びナイロン共重
合体(CM8000東レ)7重量部をエタノール90重
量部に加え、ボールミル分散した。Comparative Example 5 A conductive elastic layer of a transfer charging member was prepared in the same manner as in Example 5. Next, conductive carbon (Conductex C-90
0 (manufactured by Columbia Carbon) and 7 parts by weight of a nylon copolymer (CM8000 manufactured by Toray Industries) were added to 90 parts by weight of ethanol and dispersed in a ball mill.
【0102】前記転写帯電用部材の導電性弾性層の上に
浸漬塗工し、乾燥後膜厚200μmの樹脂層を設け、ロ
ーラー形状転写帯電用部材を製造した。A roller-shaped transfer charging member was manufactured by dip coating on the conductive elastic layer of the transfer charging member and providing a resin layer with a thickness of 200 μm after drying.
【0103】これを実施例5と同様に初期の電位測定、
及び画像を評価し、表2に示した。さらに5000枚の
画像を繰り返しとって耐久後の電位測定及び画像を検討
した。[0103] In the same manner as in Example 5, initial potential measurement,
and images were evaluated and shown in Table 2. Furthermore, 5,000 images were repeatedly taken, and the potential measurement and images after durability were examined.
【0104】比較例6
実施例5と同様に転写帯電用部材の導電性弾性層を用意
した。次にポリテトラフルオロエチレン微粉末(ルブロ
ンL−2ダイキン製)2重量部及びナイロン共重合体(
CM8000東レ製)8重量部をエタノール90重量部
に加えボールミル分散した。Comparative Example 6 A conductive elastic layer of a transfer charging member was prepared in the same manner as in Example 5. Next, 2 parts by weight of polytetrafluoroethylene fine powder (Luburon L-2 manufactured by Daikin) and nylon copolymer (
CM8000 (manufactured by Toray)) was added to 90 parts by weight of ethanol and dispersed in a ball mill.
【0105】前記転写帯電用部材の導電性弾性層の上に
浸漬塗工し、乾燥後膜厚200μmの樹脂層を設け、ロ
ーラー形状転写帯電用部材を製造した。これを比較例5
と同様に評価し、表2に示した。A roller-shaped transfer charging member was manufactured by dip coating on the conductive elastic layer of the transfer charging member and providing a resin layer with a thickness of 200 μm after drying. Comparative example 5
The results are shown in Table 2.
【0106】比較例7
実施例5と同様に転写帯電用部材の導電性弾性層を用意
した。次にポリフッ化ビニリデン微粉末(カイナー巴工
業)2重量部及びポリビニルブチラール(エスレックB
X−1積水化学製)8重量部をメチルエチルケトン90
重量部に加え、ボールミル分散した。Comparative Example 7 A conductive elastic layer of a transfer charging member was prepared in the same manner as in Example 5. Next, 2 parts by weight of polyvinylidene fluoride fine powder (Kyner Tomoe Industries) and polyvinyl butyral (S-LEC B) were added.
8 parts by weight of X-1 Sekisui Chemical) and 90 parts by weight of methyl ethyl ketone
In addition to parts by weight, the mixture was dispersed in a ball mill.
【0107】前記転写帯電用部材の導電性弾性層の上に
浸漬塗工し、乾燥後膜厚200μmの樹脂層を設け、ロ
ーラー形状転写帯電用部材を製造した。これを比較例5
と同様に評価し、表2に示した。A roller-shaped transfer charging member was manufactured by dip coating on the conductive elastic layer of the transfer charging member and providing a resin layer with a thickness of 200 μm after drying. Comparative example 5
The results are shown in Table 2.
【0108】比較例8
実施例5と同様に転写帯電用部材の導電性弾性層を用意
した。次にポリビニルブチラール(エスレックBX−1
積水化学)10重量部をメチルエチルケトン90重量部
に溶解し、前記転写帯電用部材の導電性弾性層の上に浸
漬塗工し、乾燥後膜厚200μmの樹脂層を設け、ロー
ラー形状転写帯電用部材を製造した。これを比較例5と
同様に評価し、表2に示した。Comparative Example 8 A conductive elastic layer of a transfer charging member was prepared in the same manner as in Example 5. Next, polyvinyl butyral (S-LEC BX-1
Sekisui Chemical) 10 parts by weight was dissolved in 90 parts by weight of methyl ethyl ketone, dip coated on the conductive elastic layer of the transfer charging member, and after drying, a resin layer with a film thickness of 200 μm was provided to form a roller shape transfer charging member. was manufactured. This was evaluated in the same manner as Comparative Example 5 and shown in Table 2.
【0109】実施例5、6、7、8と比較例5、8を比
較してわかるように本発明では耐久時の帯電部材のトナ
ー汚れによるフィルミングを防止し、濃度薄、白ヌケ等
の画像欠陥の発生を防止できる。As can be seen by comparing Examples 5, 6, 7, and 8 with Comparative Examples 5 and 8, the present invention prevents filming due to toner stains on the charging member during durability, and prevents problems such as thin density and white spots. Image defects can be prevented from occurring.
【0110】また、実施例5、6、7、8と比較例8を
比較してわかるように帯電部材と感光体との融着を防止
し、横スジ欠陥画像の発生を抑えることができる。Furthermore, as can be seen by comparing Examples 5, 6, 7, and 8 with Comparative Example 8, it is possible to prevent fusion between the charging member and the photoreceptor, and to suppress the occurrence of horizontal stripe defect images.
【0111】比較例6、7では樹脂の潤滑性添加剤を用
いており、耐久時に転写性能が劣化し、濃度低下を発生
している。次に除電帯電器としての特性を調べた。In Comparative Examples 6 and 7, a resin lubricating additive was used, and the transfer performance deteriorated during durability, resulting in a decrease in density. Next, we investigated its characteristics as a static eliminator.
【0112】実施例9
実施例1と同様にして感光体を作製した。次にクロロプ
レンゴム100重量部に導電性カーボン5重量部を熔融
混練し、中心に2mm×260mmのステンレス板の上
に図3のように自由長10mm×240mmになるよう
に成型し、ブレード形状帯電用部材の導電性弾性層を設
けた。この除電帯電用部材の体積抵抗を温度22℃、湿
度60%の環境で測ると4×104Ωcmである。Example 9 A photoreceptor was produced in the same manner as in Example 1. Next, 100 parts by weight of chloroprene rubber and 5 parts by weight of conductive carbon were melt-kneaded and molded onto a stainless steel plate of 2 mm x 260 mm in the center to have a free length of 10 mm x 240 mm as shown in Figure 3, and the blade shape was charged. A conductive elastic layer was provided for the member. The volume resistivity of this charge-eliminating member is 4×10 4 Ωcm when measured in an environment of a temperature of 22° C. and a humidity of 60%.
【0113】次にLMタイプグラファイト質炭素繊維(
径2μm,長200μm)3重量部及びナイロン共重合
体(CM8000東レ)7重量部をエタノール90重量
部に加え、ボールミルにて分散した。Next, LM type graphitic carbon fiber (
3 parts by weight (2 μm in diameter, 200 μm in length) and 7 parts by weight of a nylon copolymer (CM8000 Toray) were added to 90 parts by weight of ethanol and dispersed in a ball mill.
【0114】前記除電帯電用部材の導電性弾性層の上に
浸漬塗工し、乾燥後膜厚100μmの樹脂層を設け、図
3に示すようなブレード形状除電帯電用部材を製造した
。アルミシート上に同様に樹脂層を設け、体積抵抗を測
定した。[0114] A resin layer having a thickness of 100 μm was applied by dip coating on the conductive elastic layer of the above-mentioned static elimination/charging member, and after drying, a blade-shaped static elimination/charging member as shown in FIG. 3 was manufactured. A resin layer was similarly provided on the aluminum sheet, and the volume resistance was measured.
【0115】この除電帯電用部材を図6のように正現像
方式複写機PC−20キヤノン製)の前露光除電器の代
わりに取り付け、除電帯電は交流ピーク間電圧1000
Vを印加し、画像及び除電帯電部材の状態を検討した。
結果を表3に示した。さらに10000枚の画像を繰り
返しとって耐久後の電位測定及び画像を検討した。[0115] As shown in Fig. 6, this static eliminator charging member is attached in place of the pre-exposure static eliminator of a normal development type copying machine PC-20 (manufactured by Canon), and the static eliminator is charged at an AC peak-to-peak voltage of 1000.
V was applied, and the image and the state of the static eliminating charging member were examined. The results are shown in Table 3. Further, 10,000 images were repeatedly taken, and the potential measurement and images after durability were examined.
【0116】実施例10
実施例9と同様に除電帯電用部材の導電性弾性層を用意
した。次にLMタイプグラファイト質炭素繊維(径4μ
m,長500μm)4重量部及びメトキシメチル化ナイ
ロン−6(メトキシメチル化率28%)6重量部をエタ
ノール90重量部に加え、ボールミル分散した。Example 10 In the same manner as in Example 9, a conductive elastic layer of a static electricity removal/charging member was prepared. Next, LM type graphitic carbon fiber (diameter 4μ
6 parts by weight of methoxymethylated nylon-6 (methoxymethylation rate 28%) were added to 90 parts by weight of ethanol and dispersed in a ball mill.
【0117】前記除電帯電用部材の導電性弾性層の上に
浸漬塗工し、乾燥後膜厚100μmの樹脂層を設け、ブ
レード形状除電帯電用部材を製造した。これを実施例9
と同様に評価し、表3に示した。[0117] A blade-shaped static elimination/charging member was manufactured by dip coating on the conductive elastic layer of the static elimination/charging member and providing a resin layer with a thickness of 100 μm after drying. Example 9
The results were evaluated in the same manner as above and shown in Table 3.
【0118】実施例11
実施例9と同様に除電帯電用部材の導電性弾性層を用意
した。次にHSタイプ炭素繊維(径4μm,長1000
μm)2重量部及びポリビニルブチラール(BX−1積
水化学)8重量部をメチルエチルケトン90重量部に加
え、ボールミル分散した。Example 11 In the same manner as in Example 9, a conductive elastic layer of a static electricity removal/charging member was prepared. Next, HS type carbon fiber (diameter 4 μm, length 1000
2 parts by weight of polyvinyl butyral (BX-1 Sekisui Chemical) were added to 90 parts by weight of methyl ethyl ketone and dispersed in a ball mill.
【0119】前記除電帯電用部材の導電性弾性層の上に
浸漬塗工し、乾燥後膜厚100μmの樹脂層を設け、ブ
レード形状転写帯電用部材を製造した。これを実施例9
と同様に評価し、表3に示した。[0119] A resin layer having a thickness of 100 μm was provided by dip coating on the conductive elastic layer of the above-mentioned charge-eliminating charging member to produce a blade shape transfer charging member. Example 9
The results were evaluated in the same manner as above and shown in Table 3.
【0120】実施例12
実施例9と同様に除電帯電用部材の導電性弾性層を用意
した。次にHMタイプ炭素繊維(径8μm,長5000
μm)4重量部及び塩ビ、酢ビ共重合体(VMCH,U
CC製)6重量部をメチルエチルケトン90重量部に加
えボールミル分散した。Example 12 In the same manner as in Example 9, a conductive elastic layer of a static elimination/charging member was prepared. Next, HM type carbon fiber (diameter 8 μm, length 5000
μm) 4 parts by weight and vinyl chloride, vinyl acetate copolymer (VMCH, U
(manufactured by CC) were added to 90 parts by weight of methyl ethyl ketone and dispersed in a ball mill.
【0121】前記除電帯電用部材の導電製弾性層の上に
浸漬塗工し、乾燥後膜厚100μmの樹脂層を設け、ブ
レード形状除電帯電用部材を製造した。これを実施例9
と同様に評価し、表3に示した。[0121] A blade-shaped static elimination/charging member was manufactured by dip coating on the conductive elastic layer of the static elimination/charging member and providing a resin layer with a thickness of 100 μm after drying. Example 9
The results were evaluated in the same manner as above and shown in Table 3.
【0122】比較例9
実施例9と同様に除電帯電用部材の導電製弾性層を用意
した。次に導電性カーボン(コンダクテックスC−90
0コロンビアンカーボン製)3重量部及びナイロン共重
合体(CM8000東レ)7重量部をエタノール90重
量部に加えボールミル分散した。これを実施例9と同様
に初期の電位測定及び画像評価し、表3に示した。さら
に5000枚の画像を繰り返しとって耐久後の電位測定
及び画像を検討した。Comparative Example 9 In the same manner as in Example 9, a conductive elastic layer of a static electricity removal/charging member was prepared. Next, conductive carbon (Conductex C-90
0 (manufactured by Columbia Carbon) and 7 parts by weight of a nylon copolymer (CM8000 manufactured by Toray Industries) were added to 90 parts by weight of ethanol and dispersed in a ball mill. This was subjected to initial potential measurement and image evaluation in the same manner as in Example 9, and the results are shown in Table 3. Furthermore, 5,000 images were repeatedly taken, and the potential measurement and images after durability were examined.
【0123】比較例10
実施例9と同様に除電帯電用部材の導電性弾性層を用意
した。次にポリテトラフルオロエチレン微粉末(ルブロ
ンL−2ダイキン製)2重量部及びナイロン共重合体(
CM8000東レ製)8重量部をエタノール90重量部
に加え、ボールミル分散した。Comparative Example 10 In the same manner as in Example 9, a conductive elastic layer of a static electricity removal/charging member was prepared. Next, 2 parts by weight of polytetrafluoroethylene fine powder (Luburon L-2 manufactured by Daikin) and nylon copolymer (
CM8000 (manufactured by Toray Industries)) was added to 90 parts by weight of ethanol and dispersed in a ball mill.
【0124】前記除電帯電用部材の導電性弾性層の上に
浸漬塗工し、乾燥後膜厚100μmの樹脂層を設け、ブ
レード形状除電帯電用部材を製造した。これを比較例9
と同様に評価し、表3に示した。[0124] A blade-shaped static elimination/charging member was manufactured by dip coating on the conductive elastic layer of the static elimination/charging member and providing a resin layer with a thickness of 100 μm after drying. Comparative Example 9
The results were evaluated in the same manner as above and shown in Table 3.
【0125】比較例11
実施例9と同様に除電帯電用部材の導電性弾性層を用意
した。次にポリフッ化ビニリデン微粉末(カイナー,巴
工業製)2重量部及びポリビニルブチラール(エスレッ
クBX−1積水化学製)8重量部をメチルエチルケトン
90重量部に加えボールミル分散した。Comparative Example 11 In the same manner as in Example 9, a conductive elastic layer of a static electricity removal/charging member was prepared. Next, 2 parts by weight of polyvinylidene fluoride fine powder (Kynar, manufactured by Tomoe Kogyo) and 8 parts by weight of polyvinyl butyral (S-LEC BX-1 manufactured by Sekisui Chemical) were added to 90 parts by weight of methyl ethyl ketone and dispersed in a ball mill.
【0126】前記除電帯電用部材の導電性弾性層の上に
浸漬塗工し、乾燥後膜厚100μmの樹脂層を設け、ブ
レード形状除電帯電用部材を製造した。これを比較例9
と同様に評価し、表3に示した。[0126] A blade-shaped static elimination/charging member was manufactured by dip coating on the conductive elastic layer of the static elimination/charging member and providing a resin layer with a thickness of 100 μm after drying. Comparative Example 9
The results were evaluated in the same manner as above and shown in Table 3.
【0127】比較例12
実施例9と同様に除電帯電用部材の導電性弾性層を用意
した。次にポリビニルブチラール(エスレックBX−1
積水化学製)10重量部をメチルエチルケトン90重量
部に溶解し、前記除電帯電用部材の導電性弾性層の上に
浸漬塗工し、乾燥後膜厚100μmの樹脂層を設け、ブ
レード状除電帯電用部材を製造した。これを比較例9と
同様に評価し、表3に示した。Comparative Example 12 In the same manner as in Example 9, a conductive elastic layer of a static elimination/charging member was prepared. Next, polyvinyl butyral (S-LEC BX-1
Sekisui Chemical) 10 parts by weight of methyl ethyl ketone was dissolved in 90 parts by weight of methyl ethyl ketone, dip coated on the conductive elastic layer of the static elimination charging member, and after drying, a resin layer with a film thickness of 100 μm was provided. The parts were manufactured. This was evaluated in the same manner as Comparative Example 9 and shown in Table 3.
【0128】実施例9、10、11、12と比較例9、
12を比較してわかるように本発明では耐久時の帯電部
材のトナー汚れによるフィルミングを防止し、残留電位
をおさえ、地カブリの発生を防止できる。また、実施例
9、10、11、12と比較例12を比較してわかるよ
うに帯電部材と感光体との融着を防止し、横スジ欠陥画
像の発生を抑えることができる。比較例10、11では
樹脂の潤滑性添加剤を用いており、耐久時に除電性能が
劣化し、縦スジ欠陥画像を発生している。Examples 9, 10, 11, 12 and Comparative Example 9,
As can be seen by comparing No. 12, the present invention can prevent filming due to toner stains on the charging member during durability, suppress residual potential, and prevent background fogging. Furthermore, as can be seen by comparing Examples 9, 10, 11, and 12 with Comparative Example 12, it is possible to prevent the charging member from fusing with the photoreceptor and to suppress the occurrence of horizontal streak defect images. In Comparative Examples 10 and 11, a resin lubricating additive was used, and the static elimination performance deteriorated during durability, resulting in vertical streak defect images.
【0129】[0129]
【表1】[Table 1]
【0130】[0130]
【表2】[Table 2]
【0131】[0131]
【表3】 抵抗測定方法。[Table 3] How to measure resistance.
【0132】導電性弾性層の抵抗は図9に示す方法で測
定した:すなわち帯電部材を導電性の枠型にはさみ、芯
金と枠型に直流電圧1kVを印加して抵抗を測定し、堆
積抵抗値を求める。The resistance of the conductive elastic layer was measured by the method shown in FIG. 9: the charging member was sandwiched between conductive frames, the resistance was measured by applying a DC voltage of 1 kV to the core metal and the frame, and Find the resistance value.
【0133】図9中で、201は帯電部材の芯金、20
2は帯電部材の導電性弾性層、203は枠型、204は
導線、205は抵抗計である。In FIG. 9, 201 is a core metal of a charging member;
2 is a conductive elastic layer of the charging member, 203 is a frame, 204 is a conductive wire, and 205 is a resistance meter.
【0134】樹脂層の体積抵抗は、アルミニウムシート
上に樹脂層材料を設け、ヒューレット・パッカード社製
抵抗計(16008A)にて、直流電圧1kVを印加し
て、体積抵抗値を求める。The volume resistance of the resin layer is determined by providing the resin layer material on an aluminum sheet and applying a DC voltage of 1 kV using a resistance meter (16008A) manufactured by Hewlett-Packard.
【0135】[0135]
【発明の効果】以上に説明したように、本発明の帯電用
部材は、導電性弾性層上に炭素繊維を混入した樹脂層を
設けたことにより、電子写真感光体との付着性が少なく
、かつ良好な柔軟性を有し、このため電子写真装置ある
いは複写機に適用した場合、トナーの汚れも少なく、低
温低湿下でも樹脂層の体積抵抗の変動が少ないため、高
画質の画像を与える。また耐久性にも優れ、上記の効果
を長期にわたって持続することができる。As explained above, the charging member of the present invention has a resin layer mixed with carbon fiber on the conductive elastic layer, so that it has less adhesion to the electrophotographic photoreceptor. It also has good flexibility, and therefore, when applied to an electrophotographic device or a copying machine, there is little toner staining and there is little variation in the volume resistivity of the resin layer even under low temperature and low humidity, so it provides high quality images. It also has excellent durability and can maintain the above effects for a long period of time.
【図1】本発明の一実施例によるローラー形状の帯電用
部材を示す縦断面図。FIG. 1 is a longitudinal sectional view showing a roller-shaped charging member according to an embodiment of the present invention.
【図2】本発明の他の実施例による他のローラー形状の
帯電用部材を示す縦断面図。FIG. 2 is a longitudinal sectional view showing another roller-shaped charging member according to another embodiment of the present invention.
【図3】本発明さらに他の実施例によるブレード形状の
帯電用部材を示す縦断面図。FIG. 3 is a longitudinal sectional view showing a blade-shaped charging member according to still another embodiment of the present invention.
【図4】図1または図2に示した本発明の帯電用部材を
設けた電子写真装置の概略的縦断面図。4 is a schematic vertical sectional view of an electrophotographic apparatus provided with the charging member of the present invention shown in FIG. 1 or 2. FIG.
【図5】図1または図2に示した本発明の帯電用部材を
転写帯電用として設けた電子写真装置の概略的縦断面図
。FIG. 5 is a schematic vertical sectional view of an electrophotographic apparatus provided with the charging member of the present invention shown in FIG. 1 or 2 for transfer charging.
【図6】図3の帯電用部材を設けた正現像方式複写機の
概略的縦断面図。6 is a schematic vertical sectional view of a normal development type copying machine provided with the charging member of FIG. 3; FIG.
【図7】ドラム型感光体を用いた一般的な転写式電子写
真装置の概略的縦断面図。FIG. 7 is a schematic vertical cross-sectional view of a general transfer type electrophotographic apparatus using a drum-type photoreceptor.
【図8】図7の装置の構成を示すブロック図。FIG. 8 is a block diagram showing the configuration of the device in FIG. 7.
【図9】導電性弾性層の体積抵抗を求める方法を示す説
明図。FIG. 9 is an explanatory diagram showing a method for determining the volume resistance of a conductive elastic layer.
1 導電性支持体 2 導電性弾性層 3 樹脂層 4 保護層 5 粒子 6 一次帯電用部材 7 像露光手段 8 現像手段 9 転写帯電手段 10 クリーニング手段 11 前露光手段 12 感光体 13 被転写部材 14 一次帯電用コロナ帯電器 15,16 帯電部材 1 Conductive support 2 Conductive elastic layer 3 Resin layer 4 Protective layer 5 Particles 6 Primary charging member 7 Image exposure means 8 Developing means 9 Transfer charging means 10 Cleaning means 11 Pre-exposure means 12 Photoreceptor 13 Transferred member 14 Corona charger for primary charging 15, 16 Charging member
Claims (4)
た導電性弾性体からなる帯電用部材において、導電性弾
性体の上に、炭素繊維を含有する樹脂層を設けたことを
特徴とする帯電用部材。[Claim 1] A charging member comprising a conductive support and a conductive elastic body provided thereon, characterized in that a resin layer containing carbon fiber is provided on the conductive elastic body. Charging member.
最外層に有している請求項1記載の帯電用部材。2. The charging member according to claim 1, further comprising a protective layer as an outermost layer for protecting the resin layer.
mの範囲の体積抵抗率を有している請求項1または2に
記載の帯電用部材。3. The resin layer has a resistance of 10 6 to 10 12 Ω·c.
The charging member according to claim 1 or 2, having a volume resistivity in the range of m.
範囲内である請求項1から3のいづれか1項に記載の帯
電用部材。4. The charging member according to claim 1, wherein the thickness of the resin layer is within a range of 5 to 500 μm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9604691A JP2929558B2 (en) | 1991-04-03 | 1991-04-03 | Charging member |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9604691A JP2929558B2 (en) | 1991-04-03 | 1991-04-03 | Charging member |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04306673A true JPH04306673A (en) | 1992-10-29 |
JP2929558B2 JP2929558B2 (en) | 1999-08-03 |
Family
ID=14154537
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9604691A Expired - Fee Related JP2929558B2 (en) | 1991-04-03 | 1991-04-03 | Charging member |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2929558B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004081671A1 (en) * | 1995-09-05 | 2004-09-23 | Hiroshi Nagame | Device for electrically charging photosensitive body |
JP2021091553A (en) * | 2019-12-03 | 2021-06-17 | 株式会社トライテック | Transport roller and method of manufacturing the same |
-
1991
- 1991-04-03 JP JP9604691A patent/JP2929558B2/en not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004081671A1 (en) * | 1995-09-05 | 2004-09-23 | Hiroshi Nagame | Device for electrically charging photosensitive body |
JP2021091553A (en) * | 2019-12-03 | 2021-06-17 | 株式会社トライテック | Transport roller and method of manufacturing the same |
Also Published As
Publication number | Publication date |
---|---|
JP2929558B2 (en) | 1999-08-03 |
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