JP2003098818A - Developer carrier and developing machine - Google Patents
Developer carrier and developing machineInfo
- Publication number
- JP2003098818A JP2003098818A JP2001245468A JP2001245468A JP2003098818A JP 2003098818 A JP2003098818 A JP 2003098818A JP 2001245468 A JP2001245468 A JP 2001245468A JP 2001245468 A JP2001245468 A JP 2001245468A JP 2003098818 A JP2003098818 A JP 2003098818A
- Authority
- JP
- Japan
- Prior art keywords
- developer
- carrying member
- latent image
- elastic layer
- adsorbent
- 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
- 239000000126 substance Substances 0.000 claims abstract description 7
- 239000003463 adsorbent Substances 0.000 claims description 30
- 239000000463 material Substances 0.000 claims description 24
- 229920001971 elastomer Polymers 0.000 claims description 18
- 239000005060 rubber Substances 0.000 claims description 16
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 12
- 229920002379 silicone rubber Polymers 0.000 claims description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000004945 silicone rubber Substances 0.000 claims description 5
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- 239000006260 foam Substances 0.000 claims description 3
- 229910052749 magnesium Inorganic materials 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 2
- 239000004927 clay Substances 0.000 claims description 2
- 239000000499 gel Substances 0.000 claims description 2
- 239000000395 magnesium oxide Substances 0.000 claims description 2
- 239000000741 silica gel Substances 0.000 claims description 2
- 229910002027 silica gel Inorganic materials 0.000 claims description 2
- 150000004760 silicates Chemical class 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- 239000010457 zeolite Substances 0.000 claims description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims 1
- 229910021536 Zeolite Inorganic materials 0.000 claims 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims 1
- 238000011109 contamination Methods 0.000 abstract description 13
- 230000002745 absorbent Effects 0.000 abstract 1
- 239000002250 absorbent Substances 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 46
- 239000000203 mixture Substances 0.000 description 15
- 239000011162 core material Substances 0.000 description 12
- -1 polyol compound Chemical class 0.000 description 12
- 238000000034 method Methods 0.000 description 9
- 229910052799 carbon Inorganic materials 0.000 description 8
- 239000011247 coating layer Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 239000006258 conductive agent Substances 0.000 description 7
- 239000000356 contaminant Substances 0.000 description 7
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 230000001105 regulatory effect Effects 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 229920006311 Urethane elastomer Polymers 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229920002857 polybutadiene Polymers 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- 239000005062 Polybutadiene Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 229910000906 Bronze Inorganic materials 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 229920002943 EPDM rubber Polymers 0.000 description 2
- 239000004944 Liquid Silicone Rubber Substances 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Chemical class [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 2
- 239000010974 bronze Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 229920003244 diene elastomer Polymers 0.000 description 2
- VICYBMUVWHJEFT-UHFFFAOYSA-N dodecyltrimethylammonium ion Chemical compound CCCCCCCCCCCC[N+](C)(C)C VICYBMUVWHJEFT-UHFFFAOYSA-N 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 239000003344 environmental pollutant Substances 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 150000003840 hydrochlorides Chemical class 0.000 description 2
- ICIWUVCWSCSTAQ-UHFFFAOYSA-N iodic acid Chemical class OI(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 231100000719 pollutant Toxicity 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 102220057728 rs151235720 Human genes 0.000 description 2
- 239000003566 sealing material Substances 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 229920006132 styrene block copolymer Polymers 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- PDSVZUAJOIQXRK-UHFFFAOYSA-N trimethyl(octadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)C PDSVZUAJOIQXRK-UHFFFAOYSA-N 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000006237 Intermediate SAF Substances 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241000282320 Panthera leo Species 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- YOUGRGFIHBUKRS-UHFFFAOYSA-N benzyl(trimethyl)azanium Chemical compound C[N+](C)(C)CC1=CC=CC=C1 YOUGRGFIHBUKRS-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- RLGQACBPNDBWTB-UHFFFAOYSA-N cetyltrimethylammonium ion Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)C RLGQACBPNDBWTB-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229920005558 epichlorohydrin rubber Polymers 0.000 description 1
- NRJXUPLBIUZXLW-UHFFFAOYSA-N ethene;prop-1-ene;styrene Chemical compound C=C.CC=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 NRJXUPLBIUZXLW-UHFFFAOYSA-N 0.000 description 1
- 150000005452 ethyl sulfates Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920002681 hypalon Polymers 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- 239000003273 ketjen black Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000113 methacrylic resin Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- DAZXVJBJRMWXJP-UHFFFAOYSA-N n,n-dimethylethylamine Chemical compound CCN(C)C DAZXVJBJRMWXJP-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- MOFOBJHOKRNACT-UHFFFAOYSA-N nickel silver Chemical compound [Ni].[Ag] MOFOBJHOKRNACT-UHFFFAOYSA-N 0.000 description 1
- 239000010956 nickel silver Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 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
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 239000002296 pyrolytic carbon Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 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
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- PPPHYGCRGMTZNA-UHFFFAOYSA-N trifluoromethyl hydrogen sulfate Chemical class OS(=O)(=O)OC(F)(F)F PPPHYGCRGMTZNA-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Landscapes
- Dry Development In Electrophotography (AREA)
- Rolls And Other Rotary Bodies (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、複写機、ファクシ
ミリ、プリンター等の電子写真方式あるいは静電記録方
式の画像形成装置において、表面に現像剤を担持してこ
れを搬送し、感光ドラム等の潜像保持体に現像剤を供給
して潜像保持体上の静電潜像を現像するための現像剤担
持体、及び該現像剤担持体を用いた現像装置に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrophotographic or electrostatic recording type image forming apparatus such as a copying machine, a facsimile or a printer, which carries a developer on a surface thereof and conveys the developer, thereby forming a photosensitive drum or the like. The present invention relates to a developer carrier for supplying a developer to a latent image carrier to develop an electrostatic latent image on the latent image carrier, and a developing device using the developer carrier.
【0002】[0002]
【従来の技術】従来、複写機、プリンター等の電子写真
方式の画像形成装置等において、静電潜像を保持した感
光ドラム等の潜像保持体に、現像剤を供給し、現像剤を
潜像に付着させて可視化する現像方式として、加圧現像
法が知られている。2. Description of the Related Art Conventionally, in an electrophotographic image forming apparatus such as a copying machine or a printer, a developer is supplied to a latent image holding member such as a photosensitive drum that holds an electrostatic latent image, and the latent image holding member is used. A pressure developing method is known as a developing method in which an image is attached and visualized.
【0003】この加圧現像法では、例えば、図2に示し
たように、羽根状又はロール状(図ではロール状)の現
像剤供給体1により現像剤担持体2に現像剤3が供給さ
れ、この現像剤が、現像剤担持体2の表面に担持されて
現像剤担持体2の回転により搬送され、現像剤担持体2
と圧接した状態に配設された現像剤量規制ブレード4と
の間を通過する際に適正厚さの薄層に規制されると同時
に現像剤量規制ブレード4との摩擦により適正電位に帯
電し、現像剤担持体2に接触した状態に配設された潜像
保持体5へと供給され、該潜像保持体5の表面に形成さ
れた静電潜像に付着して静電潜像が可視化(現像)され
るものである。なお、図2中6は現像剤担持体2の端部
に沿って配設された現像剤封止材であり、この現像剤封
止材6により現像剤3の洩れを防止するようになってい
る。In this pressure developing method, for example, as shown in FIG. 2, the developer 3 is supplied to the developer carrier 2 by the blade-shaped or roll-shaped (roll-shaped in the figure) developer supply body 1. The developer carrier 2 is carried on the surface of the developer carrier 2 and conveyed by the rotation of the developer carrier 2,
Is regulated to a thin layer having an appropriate thickness when passing between the developer amount regulating blade 4 arranged in pressure contact with the developer amount regulating blade 4 and at the same time charged to a proper potential by friction with the developer amount regulating blade 4. , Is supplied to the latent image holding member 5 arranged in contact with the developer carrying member 2 and adheres to the electrostatic latent image formed on the surface of the latent image holding member 5 to form an electrostatic latent image. It is what is visualized (developed). Incidentally, reference numeral 6 in FIG. 2 denotes a developer sealing material arranged along the end portion of the developer carrier 2, and the developer sealing material 6 prevents the developer 3 from leaking. There is.
【0004】ここで、近年、複写機、ファクシミリ、プ
リンター等の電子写真方式或いは静電記録方式の画像形
成装置では、カラー化や画像品質の向上のために現像剤
が微粒子化され、また機器の省電力化のために現像剤が
低融点化されることに伴って、上記現像剤担持体2上の
現像剤が、上記現像剤量規制ブレード4や現像剤供給体
1との当接面でダメージを受ける問題が深刻化してい
る。このため、この現像剤のダメージを低減する目的
で、現像剤担持体2の低硬度化が求められている。In recent years, in electrophotographic type or electrostatic recording type image forming apparatuses such as copiers, facsimiles, printers, etc., the developer is made into fine particles for the purpose of colorization and improvement of image quality. Along with the lowering of the melting point of the developer for power saving, the developer on the developer carrying member 2 is contacted with the developer amount regulating blade 4 and the developer supplying member 1 at the contact surface. The problem of taking damage is getting serious. Therefore, in order to reduce the damage of the developer, it is required to reduce the hardness of the developer carrier 2.
【0005】一般に、上記現像剤担持体2は、リン青
銅、ステンレス鋼、アルミニウム、鉄等の金属からなる
芯材の外周に、樹脂、ゴム、エラストマー等からなる弾
性体層が少なくとも1層形成された構成となっており、
該弾性体層を形成する主材料としては、ジエン系ゴム、
ウレタンゴム、EPDM、シリコーンゴム等のゴム材
や、ポリオール化合物をポリイソシアネート化合物で硬
化してなるウレタンエラストマー等が使用されている。Generally, in the developer carrying member 2, at least one elastic layer made of resin, rubber, elastomer or the like is formed on the outer periphery of a core material made of metal such as phosphor bronze, stainless steel, aluminum or iron. It is configured as
As a main material for forming the elastic layer, a diene rubber,
Rubber materials such as urethane rubber, EPDM, and silicone rubber, and urethane elastomers obtained by curing a polyol compound with a polyisocyanate compound are used.
【0006】しかしながら、上記材料で低硬度の弾性体
層を形成して現像材担持体を作製した場合、潜像保持体
等の密着部分を汚染してしまうという問題が発生する。
これは、上記材料で低硬度化を実現するために、低分子
量成分の導入や硬化物の反応点を少なくする方法が採ら
れるためで、これにより増加した、硬化物の形成時に反
応に寄与しない未反応成分や、材料自体に含まれる低分
子量成分が、潜像保持体等との密着部分にブリードアウ
トして汚染が発生するものである。However, when a developer bearing member is manufactured by forming an elastic layer having a low hardness with the above materials, there arises a problem that the contact portion such as the latent image holding member is contaminated.
This is because in order to achieve low hardness in the above materials, a method of introducing a low molecular weight component or reducing the reaction points of the cured product is adopted, which does not contribute to the reaction that is increased when the cured product is formed. Unreacted components and low-molecular-weight components contained in the material itself bleed out to the area where they are in close contact with the latent image carrier and cause contamination.
【0007】本発明は、上記事情に鑑みなされたもの
で、電子写真方式や静電記録方式の画像形成装置におい
て、現像剤供給部材から供給される現像剤を表面に担持
して搬送し、潜像保持体に形成された静電潜像に現像剤
を供給することにより、静電潜像を現像する現像剤担持
体について、弾性層の低硬度化を達成しえると共に、こ
れに密着する他部材の汚染を効果的に防止しえる技術を
提供することを目的とする。The present invention has been made in view of the above circumstances, and in an electrophotographic or electrostatic recording type image forming apparatus, the developer supplied from a developer supply member is carried on the surface and conveyed, By supplying a developer to the electrostatic latent image formed on the image carrier, the hardness of the elastic layer of the developer carrier for developing the electrostatic latent image can be reduced and the developer can be adhered to it. It is an object of the present invention to provide a technique capable of effectively preventing contamination of members.
【0008】[0008]
【課題を解決するための手段及び発明の実施の形態】本
発明者は、上記目的を達成するため鋭意検討を行った結
果、芯体の外周に少なくとも1層の弾性層を形成して現
像剤担持体を得る場合に、該弾性層中に汚染物質を吸着
する吸着剤を分散させて、該弾性層からの汚染物質のブ
リードアウトを防止することを見出し、更に検討を進め
た結果、上記吸着剤の比表面積を0.4m2/g以上と
し、この吸着剤の配合量を、弾性層を形成する高分子物
質成分100重量部に対して0.5〜100重量部の範
囲とすることにより、弾性層中の汚染物質を良好に吸着
して汚染物質のブリードアウトを効果的に防止し得、密
着部における他部材の汚染を可及的に防止し得て、低硬
度で汚染の問題を生じることのない現像剤担持体が得ら
れることを見出し、本発明を完成したものである。Means for Solving the Problems and Modes for Carrying Out the Invention As a result of earnest studies for achieving the above-mentioned object, the present inventor found that at least one elastic layer was formed on the outer periphery of a core body to form a developer. When obtaining a carrier, it was found that an adsorbent that adsorbs contaminants is dispersed in the elastic layer to prevent bleed-out of contaminants from the elastic layer, and as a result of further studies, the above adsorption The specific surface area of the agent is 0.4 m 2 / g or more, and the amount of the adsorbent compounded is in the range of 0.5 to 100 parts by weight with respect to 100 parts by weight of the polymeric substance component forming the elastic layer. , The contaminants in the elastic layer can be adsorbed well and the bleed-out of the contaminants can be effectively prevented, and the contamination of other members in the close contact part can be prevented as much as possible, and the problem of contamination with low hardness can be solved. We found that a developer carrier that does not occur can be obtained. One in which the present invention has been completed.
【0009】従って、本発発明は、表面に現像剤を担持
して該現像剤の薄層を形成し、これを搬送して潜像保持
体表面に形成された静電潜像に供給し、該静電潜像を現
像するための現像剤担持体において、芯体の外周に少な
くとも1層の弾性層を有し、該弾性層を構成する弾性体
中に、比表面積0.4m2/g以上の吸着剤が該弾性体
を形成する高分子物質成分100重量部に対して0.5
〜100重量部の割合で分散していることを特徴とする
現像剤担持体、及び、該現像剤担持体を具備してなるこ
とを特徴とする現像装置を提供する。Therefore, according to the present invention, a developer is carried on the surface to form a thin layer of the developer, which is conveyed and supplied to the electrostatic latent image formed on the surface of the latent image carrier, In a developer carrier for developing the electrostatic latent image, at least one elastic layer is provided on the outer periphery of a core body, and the elastic body constituting the elastic layer has a specific surface area of 0.4 m 2 / g. The amount of the above adsorbent is 0.5 with respect to 100 parts by weight of the polymeric substance component forming the elastic body.
Disclosed is a developer carrying member characterized by being dispersed in an amount of 100 to 100 parts by weight, and a developing device comprising the developer carrying member.
【0010】以下、本発明につき更に詳しく説明する。
本発明の現像剤担持体は、芯体の外周に吸着剤を分散し
た弾性層を少なくとも1層形成したものであり、例え
ば、図1に示したように、芯体7の外周に、吸着剤を分
散した弾性層8を積層形成したローラ状の現像担持体を
例示することができる。The present invention will be described in more detail below.
The developer carrying member of the present invention is one in which at least one elastic layer in which an adsorbent is dispersed is formed on the outer periphery of a core, and for example, as shown in FIG. An example is a roller-shaped development carrier in which the elastic layer 8 in which is dispersed is formed.
【0011】上記芯体7は、特に制限はなく、各種金属
や樹脂からなる中実又は中空の芯体が用いられ、例え
ば、金属としては、鉄、銅、洋白、ステンレススチー
ル、リン青銅などが例示され、また樹脂としては、ポリ
エチレン、ポリアミド、ポリアセタール、ポリカーボネ
ート、ポリエチレンテレフタレート、ポリイミド、ポリ
アミドイミド、ポリエステル、フェノール樹脂、メラミ
ン樹脂、シリコーン樹脂、エポキシ樹脂、アクリル樹
脂、メタクリル樹脂、尿素樹脂などの合成樹脂が例示さ
れる。The core body 7 is not particularly limited and may be a solid or hollow core body made of various metals or resins. Examples of the metal include iron, copper, nickel silver, stainless steel, phosphor bronze and the like. The resin is exemplified by polyethylene, polyamide, polyacetal, polycarbonate, polyethylene terephthalate, polyimide, polyamide imide, polyester, phenol resin, melamine resin, silicone resin, epoxy resin, acrylic resin, methacrylic resin, urea resin and the like. A resin is exemplified.
【0012】また、上記弾性体8を形成する主材料とし
ては、イソプレンゴム、ブタジエンゴム、スチレン・ブ
タジエンゴム、アクリロニトリル・ブタジエンコム、ク
ロロプレンゴム、エチレン・プロピレンゴム、エチレン
・プロピレンターポリマー、ブチルゴム、アクリルゴ
ム、クロルスルフォン化ポリエチレン、シリコーンゴ
ム、フッ素ゴム、ポリエーテルゴム、エピクロルヒドリ
ンゴム、ウレタンゴム等のゴム材料や、ポリオール化合
物等をポリイシソアネート化合物で硬化してなるポリウ
レタンエラストマー材料や、ポリウレタン、シリコー
ン、ポリスチレン・ポリブタジエンブロック重合体(S
BS)、スチレンエチレンブチレンスチレンブロック共
重合体(SEBS)、スチレンエチレンプロピレンスチ
レンブロック共重合体(SEPS)、ポリオレフィン、
ポリエチレン、塩素化ポリエチレン、エチレン・酢酸ビ
ニル共重合体等の熱可塑性エラストマー、及びこれらの
混合物などが例示される。中でも、弾性層をできるだけ
低硬度化するために、特にジエン系ゴム、ウレタンゴ
ム、EPDM等の有機ゴム材料やシリコーンゴム、又は
ウレタン、SBS、SEBS、SEPS等のエラストマ
ー材料が好ましく用いられ、更にこれらの中でも、容易
に低硬度で低圧縮永久歪の弾性体を形成し得ることか
ら、シリコーンゴムがより好ましく用いられる。As the main material for forming the elastic body 8, isoprene rubber, butadiene rubber, styrene / butadiene rubber, acrylonitrile / butadiene com, chloroprene rubber, ethylene / propylene rubber, ethylene / propylene terpolymer, butyl rubber, acrylic resin. Rubber materials such as rubber, chlorosulfonated polyethylene, silicone rubber, fluororubber, polyether rubber, epichlorohydrin rubber, urethane rubber, and polyurethane elastomer materials obtained by curing polyol compounds with a polyisocyanate compound, polyurethane, silicone , Polystyrene / polybutadiene block polymer (S
BS), styrene ethylene butylene styrene block copolymer (SEBS), styrene ethylene propylene styrene block copolymer (SEPS), polyolefin,
Examples thereof include thermoplastic elastomers such as polyethylene, chlorinated polyethylene, ethylene / vinyl acetate copolymer, and mixtures thereof. Among them, in order to reduce the hardness of the elastic layer as much as possible, organic rubber materials such as diene rubber, urethane rubber, EPDM and silicone rubber, or elastomer materials such as urethane, SBS, SEBS and SEPS are preferably used. Among them, silicone rubber is more preferably used because it can easily form an elastic body having a low hardness and a low compression set.
【0013】これら弾性体には、必要に応じて公知の添
加剤を配合することができ、例えばカーボン等の充填
剤、各種オイル等の可塑剤、帯電制御剤等の添加剤を本
発明の目的を逸脱しない範囲で、必要に応じて適量添加
することができる。If desired, known additives may be added to these elastic bodies. For example, fillers such as carbon, plasticizers such as various oils, and additives such as charge control agents may be used for the purpose of the present invention. An appropriate amount can be added if necessary within the range not deviating from the above.
【0014】この弾性層8は、単層でも2層以上の複数
層で構成されていてもよい。また、弾性層8の厚さ方向
の一部又は全部を発泡体としてもよく、このように発泡
体層を設けることにより、弾性層8の構成材料である上
記高分子材料自体を大幅に低硬度化する必要がなくな
り、又は上記高分子材料の低硬度化を不要にすることも
可能であり、低硬度化に伴って発生する未反応成分や低
分子量分の発生を効果的に低減化し得、より効果的に汚
染防止を図ることができる。The elastic layer 8 may be composed of a single layer or a plurality of layers of two or more layers. Further, a part or the whole of the elastic layer 8 in the thickness direction may be a foam, and by providing the foam layer in this way, the polymer material itself which is a constituent material of the elastic layer 8 has a significantly low hardness. It is also possible to eliminate the need to reduce the hardness, or to eliminate the need to reduce the hardness of the polymer material, it is possible to effectively reduce the generation of unreacted components and low molecular weight components that occur with the reduction in hardness, Contamination can be prevented more effectively.
【0015】本発明の現像剤担持体は、上記弾性層8を
構成する弾性体中に吸着剤を配合分散させたものであ
り、弾性層8を形成する低硬度材料中の未反応成分や低
分子量分の汚染物質をこの吸着剤に吸着させて、これら
汚染物質のブリードアウトを可及的に防止するものであ
る。The developer carrying member of the present invention is prepared by mixing and dispersing an adsorbent in the elastic body forming the elastic layer 8, and the unreacted component and the low content in the low hardness material forming the elastic layer 8 are reduced. By adsorbing pollutants having a molecular weight to this adsorbent, bleed-out of these pollutants is prevented as much as possible.
【0016】この吸着剤は、比表面積が0.4m2/g
以上のもが用いられ、好ましくは1m2/g以上、より
好ましくは5m2/g以上のものが用いられる。この吸
着剤としては、上記比表面積を満足するものであればい
ずれのものを用いてよく、特に制限されるものではない
が、例えば各種活性炭、ゼオライト、酸性白土、シリ
カ、シリカゲル、シリカ−アルミナゲル、アルミナ、マ
クネシアや、Mg,Al又はSiの酸化物、珪酸塩、炭
酸塩などが挙げられ、これらの1種又は2種以上を組み
合わせて用いることができる。この吸着剤の配合分散量
は、弾性層8を形成する上記高分子物質材料100重量
部に対して0.5〜100重量部とされ、好ましくは2
〜80重量部、より好ましくは5〜50重量部とされ
る。This adsorbent has a specific surface area of 0.4 m 2 / g
The above is used, preferably 1 m 2 / g or more, more preferably 5 m 2 / g or more. As the adsorbent, any adsorbent may be used as long as it satisfies the specific surface area, and is not particularly limited, and examples thereof include various activated carbons, zeolites, acid clay, silica, silica gel, silica-alumina gel. , Alumina, magnesia, oxides of Mg, Al or Si, silicates, carbonates, and the like, and one or more of these may be used in combination. The amount of the adsorbent compounded and dispersed is 0.5 to 100 parts by weight, preferably 2 to 100 parts by weight of the polymeric material forming the elastic layer 8.
˜80 parts by weight, more preferably 5 to 50 parts by weight.
【0017】ここで、上記吸着剤の比表面積が0.4m
2/g未満であると、吸着剤表面に存在する汚染物質の
吸着サイトを必要量確保するために、100重量部を超
える多量の吸着剤を必要とし、弾性層8を形成する弾性
体の物性変化を引き起こすこととなってしまう。具体的
には、低硬度材料により弾性層8を形成しても、多量の
吸着剤添加によって硬度が高くなってしまったり、圧縮
永久歪の悪化によって、現像剤量規制部材や潜像保持体
との長期圧接により現像剤担持体が変形してしまい、結
果として画像不良を発生させてしまうなどの不都合を発
生させることとなる。一方、吸着剤の配合分散量が0.
5重量部未満であると、汚染物質を十分に吸着するには
吸着サイトの総量が足りず、潜像保持体等の汚染が発生
して、本発明の目的を達成し得ない。Here, the specific surface area of the adsorbent is 0.4 m.
If it is less than 2 / g, a large amount of adsorbent exceeding 100 parts by weight is required to secure a necessary amount of adsorption sites for contaminants existing on the surface of the adsorbent, and the physical properties of the elastic body forming the elastic layer 8 are required. It will cause a change. Specifically, even if the elastic layer 8 is formed of a low-hardness material, the hardness becomes high due to the addition of a large amount of an adsorbent, or the compression set deteriorates, so that the developer amount control member or the latent image holding member is formed. Due to the long-term pressure contact, the developer bearing member is deformed, resulting in inconvenience such as image failure. On the other hand, the admixture dispersion amount of the adsorbent is 0.
If the amount is less than 5 parts by weight, the total amount of adsorption sites is insufficient to sufficiently adsorb the contaminants, and the latent image holding member or the like is contaminated, and the object of the present invention cannot be achieved.
【0018】この弾性層8は、図1では1層の例を示し
たが、複数層形成することもでき、この場合少なくとも
1層の弾性層を構成する弾性体中に上記吸着剤が分散さ
れていればよい。The elastic layer 8 is shown as an example of one layer in FIG. 1, but it is also possible to form a plurality of layers. In this case, the adsorbent is dispersed in at least one elastic body constituting the elastic layer. If you have.
【0019】また、この弾性層8には、導電性の付与又
は導電性調節のため、必要に応じて導電剤を配合するこ
とができる。導電剤としては、テトラエチルアンモニウ
ム、テトラブチルアンモニウム、ラウリルトリメチルア
ンモニウム、ステアリルトリメチルアンモニウム、オク
タデシルトリメチルアンモニウム、ドデシルトリメチル
アンモニウム、ヘキサデシルトリメチルアンモニウム、
ベンジルトリメチルアンモニウム、変性脂肪酸ジメチル
エチルアンモニウム等の過塩素酸塩、塩素酸塩、塩酸
塩、臭素酸塩、ヨウ素酸塩、ホウフッ化水素酸塩、硫酸
塩、エチル硫酸塩、カルボン酸塩、スルフォン酸塩等の
アンモニウム塩;リチウム、ナトリウム、カルシウム、
マグネシウム等のアルカリ金属或いはアルカリ土類金属
の過塩素酸塩、塩素酸塩、塩酸塩、臭素酸塩、ヨウ素酸
塩、ホウフッ化水素酸塩、トリフルオロメチル硫酸塩、
スルフォン酸塩などのイオン導電剤;ケッチェンブラッ
ク、アセチレンブラック等の導電性カーボン;SAF、
ISAF、HAF、FEF、GPF、SRF、FT、M
T等のゴム用カーボン;酸化処理を施したインク用カー
ボン、熱分解カーボン、グラファイト;酸化スズ、酸化
チタン、酸化亜鉛等の導電性金属酸化物;ニッケル、銅
等の金属などの電子導電剤が例示され、特に導電性カー
ボン、ゴム用カーボン、インク用カーボンが好適に用い
られる。In addition, a conductive agent may be added to the elastic layer 8 as needed to impart conductivity or adjust conductivity. As the conductive agent, tetraethylammonium, tetrabutylammonium, lauryltrimethylammonium, stearyltrimethylammonium, octadecyltrimethylammonium, dodecyltrimethylammonium, hexadecyltrimethylammonium,
Perchlorates such as benzyltrimethylammonium and modified fatty acid dimethylethylammonium, chlorates, hydrochlorides, bromates, iodates, borofluorides, sulfates, ethylsulfates, carboxylates, sulfonic acids Ammonium salts such as salts; lithium, sodium, calcium,
Perchlorates, chlorates, hydrochlorides, bromates, iodates, borofluorides, trifluoromethylsulfates of alkali metals or alkaline earth metals such as magnesium,
Ion conductive agents such as sulfonates; conductive carbon such as Ketjen black and acetylene black; SAF,
ISAF, HAF, FEF, GPF, SRF, FT, M
Carbon for rubber such as T; carbon for ink subjected to oxidation treatment, pyrolytic carbon, graphite; conductive metal oxide such as tin oxide, titanium oxide and zinc oxide; electronic conductive agent such as metal such as nickel and copper For example, conductive carbon, carbon for rubber, and carbon for ink are preferably used.
【0020】この導電剤の配合量は、導電剤の種類等に
応じて適宜選定され、特に制限されるものではないが、
通常は弾性層8の主材料である上記高分子物質100重
量部に対して0.01〜50重量部、特に1〜30重量
部とすることが好ましく、これにより弾性層8の電気抵
抗を102〜1011Ω・cm程度、特に104〜109Ω
・cm程度に調整することが好ましい。The amount of the conductive agent blended is appropriately selected according to the type of the conductive agent and is not particularly limited,
Usually, it is preferably 0.01 to 50 parts by weight, particularly 1 to 30 parts by weight, relative to 100 parts by weight of the above-mentioned polymer substance, which is the main material of the elastic layer 8, whereby the electric resistance of the elastic layer 8 is 10 parts by weight. 2 to 10 11 Ω · cm, especially 10 4 to 10 9 Ω
-It is preferable to adjust to about cm.
【0021】また、この弾性層8には、上記吸着剤、導
電剤の他にも、必要に応じて公知の充填剤、加硫剤、そ
の他の添加剤を本発明の目的を逸脱しない範囲で適宜添
加して差し支えない。In addition to the above-mentioned adsorbent and conductive agent, known fillers, vulcanizing agents, and other additives may be added to the elastic layer 8 if necessary, within the scope of the present invention. It may be added appropriately.
【0022】この弾性層8の硬度は、特に制限されるも
のではないが、アスカーC硬度計で20〜85、特に4
0〜75であることが好ましく、本発明の現像剤担持体
は、このような低硬度に設定しても、上記吸着剤の作用
により汚染の問題を生じることなく、良好な現像操作を
確実に行うことできるものである。The hardness of the elastic layer 8 is not particularly limited, but is 20 to 85, particularly 4 as measured by an Asker C hardness meter.
0 to 75 is preferable, and the developer carrying member of the present invention ensures a good developing operation without causing a problem of contamination due to the action of the adsorbent even when set to such a low hardness. It is something you can do.
【0023】この弾性層8の形成方法は、特に制限はな
く公知の方法を採用することができ、一般には塗布、一
体成形、押出成形、或いは予め円筒状に形成され適当な
寸法に裁断された弾性体に芯体7を挿入し接着する方法
などが採用される。なお、芯体7と弾性層8との間には
必要に応じて接着剤層を設けてもよい。The elastic layer 8 can be formed by any known method without particular limitation. Generally, it is applied, integrally molded, extruded, or previously formed into a cylindrical shape and cut into a suitable size. A method of inserting the core body 7 into the elastic body and adhering it is adopted. An adhesive layer may be provided between the core body 7 and the elastic layer 8 if necessary.
【0024】本発明の現像剤担持体は、上述のように、
芯体7の外周に吸着剤を分散した上記弾性層8を形成し
たものであるが、図1に一点鎖線で示したように、上記
弾性層8上に耐密着性向上、帯電性の最適化、摩擦係数
低減などを目的として、被覆層9を必要に応じて形成す
ることができる。The developer carrier of the present invention is, as described above,
The elastic layer 8 in which an adsorbent is dispersed is formed on the outer periphery of the core body 7. As shown by the one-dot chain line in FIG. 1, the adhesion resistance is improved and the charging property is optimized on the elastic layer 8. The coating layer 9 can be formed as necessary for the purpose of reducing the friction coefficient.
【0025】この被覆層を形成する材料としては、ポリ
エステル樹脂、ポリエーテル樹脂、フッ素樹脂、エポキ
シ樹脂、アミノ樹脂、ポリアミド樹脂、アクリル樹脂、
アクリルウレタン樹脂、ウレタン樹脂、アルキッド樹
脂、フェノール樹脂、メラミン樹脂、尿素樹脂、シリコ
ーン樹脂、ポリビニルブチラール樹脂、及びこれらの混
合物等が挙げられる。As the material for forming this coating layer, polyester resin, polyether resin, fluororesin, epoxy resin, amino resin, polyamide resin, acrylic resin,
Examples thereof include acrylic urethane resin, urethane resin, alkyd resin, phenol resin, melamine resin, urea resin, silicone resin, polyvinyl butyral resin, and mixtures thereof.
【0026】この被覆層9には、必要に応じて、カーボ
ン等の充填剤、オイル等の可塑剤、帯電制御剤等の添加
剤を本発明の目的を逸脱しない範囲で、適宜添加して差
し支えない。この被覆層9を上記弾性層8上に形成する
方法に特に制限はなく、例えば塗布、インモールドコー
ト法、或いは予め円筒状に形成されたシュリンクチュー
ブを過熱収縮させて被覆する方法などが適宜選択され
る。なお、弾性層8とこの被覆層9との間に必要に応じ
て接着剤層を設けることもできる。If necessary, a filler such as carbon, a plasticizer such as oil, an additive such as a charge control agent may be appropriately added to the coating layer 9 within a range not departing from the object of the present invention. Absent. The method for forming the coating layer 9 on the elastic layer 8 is not particularly limited, and for example, coating, in-mold coating method, or a method of coating by shrinking a shrink tube previously formed in a cylindrical shape by overheat shrinkage is appropriately selected. To be done. An adhesive layer may be provided between the elastic layer 8 and the coating layer 9 if necessary.
【0027】本発明の現像剤担持体は、電子写真装置や
静電記録装置において、潜像保持体に現像剤を供給して
潜像保持体上の静電潜像を現像するためのものであり、
例えば、図2に示された機構の現像装置に現像担持体2
として用いられるものである。なお、図2の現像装置に
ついては先に説明しているので、その詳細は省略する。The developer carrying member of the present invention is for supplying a developer to a latent image holding member to develop an electrostatic latent image on the latent image holding member in an electrophotographic apparatus or an electrostatic recording apparatus. Yes,
For example, in the developing device having the mechanism shown in FIG.
Is used as. Since the developing device in FIG. 2 has been described above, its details are omitted.
【0028】なお、本発明の現像剤担持体は、図1,2
に示されているようなローラ状の部材に限定されるもの
ではなく、用いられる現像装置の構造等に応じて適宜な
形態とすることができる。また、本発明の現像装置も、
上記図2に示したものに限定されず、表面に現像剤を担
持して該現像剤の薄層を形成し、これを搬送して潜像保
持体に供給する現像剤担持体を具備するものであれば、
その構造は図2の現像装置と異なっていてもよい。The developer carrier of the present invention is shown in FIGS.
The present invention is not limited to the roller-shaped member as shown in (1), but may have an appropriate form depending on the structure of the developing device used. Also, the developing device of the present invention,
The present invention is not limited to the one shown in FIG. 2 above, and is provided with a developer carrier that carries a developer on the surface to form a thin layer of the developer, and conveys the developer to supply it to the latent image carrier. If,
Its structure may be different from that of the developing device of FIG.
【0029】[0029]
【実施例】以下、実施例,比較例を示して本発明をより
具体的に説明するが、本発明は下記実施例に制限される
ものではない。
[実施例1]下記配合(1)の有機ゴム材料をニーダー
で混合し、モールドにて成形,加熱硬化させた後、脱
型、研磨して円筒状の芯体外周に弾性層を形成し、図1
に示した構造の現像剤担持体を得た。但し、図2中に一
点鎖線で示された被覆層9は形成しなかった。また、吸
着剤として用いたアルミナ(住友化学工業社製:「AL
M43」)の比表面積は1.2m2/gであった。更に
得られた現像剤担持体の表面硬度は、アスカーC硬度計
で68°であった。配合(1)
ポリブタジエンゴム(JSR社製:「BR18」) 75.0g
液状ポリイソプレン(クラレ社製:「LIR30」) 25.0g
導電性カーボンブラック(ライオン社製:「ケッチェンEC600JD」)
3.2g
酸化亜鉛(ハクスイテック社製:「亜鉛華1号」) 1.0g
アルミナ(住友化学工業社製:「ALM43」) 20.0g
ステアリン酸(ミヨシ油脂社製) 1.0g
加硫剤(日本油脂社製:「パーヘキサ3M−40」) 1.5gEXAMPLES The present invention will be described in more detail with reference to Examples and Comparative Examples, but the present invention is not limited to the following Examples. Example 1 An organic rubber material having the following composition (1) was mixed with a kneader, molded with a mold, cured by heating, and then demolded and polished to form an elastic layer on the outer periphery of a cylindrical core, Figure 1
A developer carrier having the structure shown in was obtained. However, the coating layer 9 indicated by the alternate long and short dash line in FIG. 2 was not formed. Alumina used as an adsorbent (manufactured by Sumitomo Chemical Co., Ltd .: “AL
The specific surface area of M43 ") was 1.2 m 2 / g. Further, the surface hardness of the obtained developer bearing member was 68 ° with an Asker C hardness meter. Blend (1) Polybutadiene rubber (JSR: “BR18”) 75.0 g Liquid polyisoprene (Kuraray: “LIR30”) 25.0 g Conductive carbon black (Lion: “Ketjen EC600JD”) 3.2 g Zinc oxide (manufactured by Huxui Tech: "Zinc Hua No. 1") 1.0 g Alumina (manufactured by Sumitomo Chemical Co., Ltd .: "ALM43") 20.0 g Stearic acid (manufactured by Miyoshi Yushi Co., Ltd.) 1.0 g Vulcanizing agent (Nippon Yushi Co., Ltd.) Product: "Perhexa 3M-40") 1.5 g
【0030】得られた現像剤担持体を、図2と同様の現
像装置に組み込んで、高温高湿下(50℃,90%)に
7日間放置したところ、潜像担持体との当接面に汚染は
見られなかった。一方、この現像装置を画像形成装置に
装着して印刷テストを行ったところ、良好な画像が得ら
れた。また、別途同様にして作製した現像剤担持体を現
像装置に組み込んで潜像保持体に圧接した状態で4週間
放置した後、印刷テストを行ったところ、良好な画像が
得られた。The obtained developer bearing member was installed in a developing device similar to that shown in FIG. 2 and left under high temperature and high humidity (50 ° C., 90%) for 7 days. No pollution was found in the. On the other hand, when the developing device was attached to the image forming apparatus and a printing test was conducted, a good image was obtained. Further, a developer carrying member prepared in the same manner as described above was incorporated into a developing device, allowed to stand for 4 weeks in a state of being in pressure contact with the latent image holding member, and a printing test was carried out. As a result, a good image was obtained.
【0031】[比較例1]吸着剤のアルミナ(住友化学
工業社製:「ALM43」)を配合せず、架橋剤(日本
油脂社製:「パーヘキサ3M−40」)を2.0gに増
量した以外は上記配合(1)と同様の組成の有機ゴム材
料を用い、実施例1と同様にして現像剤担持体を得た。
得られた現像剤担持体の表面硬度は、アスカーC硬度計
で68°であった。[Comparative Example 1] The amount of the cross-linking agent (Nippon Yushi Co., Ltd .: "Perhexa 3M-40") was increased to 2.0 g without adding the adsorbent alumina (Sumitomo Chemical Co., Ltd .: "ALM43"). A developer carrying member was obtained in the same manner as in Example 1 except that the organic rubber material having the same composition as the above-mentioned formulation (1) was used except for the above.
The surface hardness of the obtained developer carrying member was 68 ° by an Asker C hardness meter.
【0032】得られた、現像剤担持体につき、実施例1
と同様の試験を行ったところ、高温高湿下での放置テス
トでは、潜像保持体との当接面に明らかな汚染が見ら
れ、また印刷テストではかかる当接部に相当する位置に
画像不良が発生した。The developer carrier thus obtained was used in Example 1.
When the same test was performed, a clear contamination was found on the contact surface with the latent image holder in the storage test under high temperature and high humidity, and in the printing test, the image was found at the position corresponding to the contact part. A defect has occurred.
【0033】[比較例2]吸着剤のアルミナを昭和電工
社製:「AS−10」に変更し、その配合量を40.0
gにした以外は上記配合(1)と同様の組成の有機ゴム
材料を用い、実施例1と同様にして現像剤担持体を得
た。吸着剤として添加した上記アルミナの比表面積は、
0.3m2/gであった。また、得られた現像剤担持体
の表面硬度は、アスカーC硬度計で68°であった。[Comparative Example 2] The adsorbent alumina was changed to "AS-10" manufactured by Showa Denko KK, and the compounding amount was 40.0.
A developer carrying member was obtained in the same manner as in Example 1 except that the organic rubber material having the same composition as the above-mentioned formulation (1) was used except that the amount was changed to g. The specific surface area of the alumina added as an adsorbent,
It was 0.3 m 2 / g. The surface hardness of the obtained developer bearing member was 68 ° with an Asker C hardness meter.
【0034】得られた、現像剤担持体につき、実施例1
と同様の試験を行ったところ、高温高湿下での放置テス
トでは、潜像保持体との当接面に明らかな汚染が見ら
れ、また印刷テストではかかる当接部に相当する位置に
画像不良が発生した。The developer carrier thus obtained was used in Example 1.
When the same test was performed, a clear contamination was found on the contact surface with the latent image holder in the storage test under high temperature and high humidity, and in the printing test, the image was found at the position corresponding to the contact part. A defect has occurred.
【0035】[比較例3]吸着剤のアルミナ(昭和電工
社製:「AS−10」)を120.0gに増量し、架橋
剤(日本油脂社製:「パーヘキサ3M−40」)を0.
8gに減量した以外は比較例2で用いた有機ゴム材料と
同様の組成の有機ゴム材料を用い、実施例1と同様にし
て現像剤担持体を得た。得られた現像剤担持体の表面硬
度は、アスカーC硬度計で70°であった。[Comparative Example 3] The adsorbent alumina (Showa Denko KK: "AS-10") was added to 120.0 g, and the cross-linking agent (NOF CORPORATION: "Perhexa 3M-40") was added to 0.
An organic rubber material having the same composition as the organic rubber material used in Comparative Example 2 was used except that the amount was reduced to 8 g, and a developer carrying member was obtained in the same manner as in Example 1. The surface hardness of the obtained developer carrying member was 70 ° on an Asker C hardness meter.
【0036】得られた、現像剤担持体につき、実施例1
と同様の試験を行ったところ、高温高湿下での放置テス
トでは、潜像保持体との当接面に汚染は見られず、印刷
テストでも良好な画像が得られた。しかしながら、潜像
保持体に圧接した状態で4週間放置した後の印刷テスト
では、印刷画像の現像剤担持体と潜像保持体との当接部
相当位置に、現像剤担持体の残留歪を原因とする画像不
良が発生した。The developer carrier thus obtained was used in Example 1.
When a test similar to the above was performed, no contamination was found on the contact surface with the latent image holding member in the standing test under high temperature and high humidity, and a good image was obtained in the printing test. However, in the printing test after leaving the latent image carrier in pressure contact for 4 weeks, the residual strain of the developer carrier was found at the position corresponding to the contact portion between the developer image carrier and the latent image carrier. The cause is a defective image.
【0037】[比較例4]吸着剤のアルミナを昭和電工
社製:「AL−43−L」に変更し、その配合量を0.
3gに減量した以外は実施例1で用いた上記配合(1)
と同様の組成の有機ゴム材料を用い、実施例1と同様に
して現像剤担持体を得た。吸着剤として添加した上記ア
ルミナの比表面積は、3.2m2/gであった。また、
得られた現像剤担持体の表面硬度は、アスカーC硬度計
で68°であった。[Comparative Example 4] The alumina of the adsorbent was changed to "AL-43-L" manufactured by Showa Denko KK, and the compounding amount was adjusted to 0.
The above formulation (1) used in Example 1 except that the amount was reduced to 3 g.
A developer carrying member was obtained in the same manner as in Example 1, using an organic rubber material having the same composition as in (1). The specific surface area of the alumina added as the adsorbent was 3.2 m 2 / g. Also,
The surface hardness of the obtained developer carrying member was 68 ° by an Asker C hardness meter.
【0038】得られた、現像剤担持体につき、実施例1
と同様の試験を行ったところ、高温高湿下での放置テス
トでは、潜像保持体との当接面に明らかな汚染が見ら
れ、また印刷テストではかかる当接部に相当する位置に
画像不良が発生した。The developer carrier thus obtained was used in Example 1.
When the same test was performed, a clear contamination was found on the contact surface with the latent image holder in the storage test under high temperature and high humidity, and in the printing test, the image was found at the position corresponding to the contact part. A defect has occurred.
【0039】[実施例2]下記配合(2)の液状シリコ
ーンゴム原料を混合し、モールドに注型して、成形,加
熱硬化させた後、脱型、研磨して円筒状の芯体外周に弾
性層を形成し、図1に示した構造の現像剤担持体を得
た。但し、図2中に一点鎖線で示された被覆層9は形成
しなかった。また、吸着剤として用いたアルミナ(住友
化学工業社製:「ALM43」)の比表面積は1.2m
2/gであった。更に得られた現像剤担持体の表面硬度
は、アスカーC硬度計で70°であった。配合(2)
液状シリコーン(東レ・ダウ・コーニング社製:「DY35−4046A」)
50.0g
液状シリコーン(東レ・ダウ・コーニング社製:「DY35−4046B」)
50.0g
アルミナ(住友化学工業社製:「ALM43」) 20.0gExample 2 A liquid silicone rubber raw material having the following composition (2) was mixed, cast into a mold, molded and heat-cured, and then demolded and polished to form a cylindrical core outer periphery. An elastic layer was formed to obtain a developer carrier having the structure shown in FIG. However, the coating layer 9 indicated by the alternate long and short dash line in FIG. 2 was not formed. Further, the specific surface area of alumina (Sumitomo Chemical Co., Ltd .: "ALM43") used as an adsorbent is 1.2 m.
It was 2 / g. Further, the surface hardness of the obtained developer bearing member was 70 ° with an Asker C hardness meter. Formulation (2) Liquid silicone (Toray Dow Corning: “DY35-4046A”) 50.0 g Liquid silicone (Toray Dow Corning: “DY35-4046B”) 50.0 g Alumina (Sumitomo Chemical Co., Ltd.) Made: "ALM43") 20.0 g
【0040】得られた、現像剤担持体につき、実施例1
と同様の試験を行ったところ、高温高湿下での放置テス
トでは、潜像保持体との当接面に汚染は見られず、印刷
テストでも良好な画像が得られた。更に潜像保持体に圧
接した状態で4週間放置した後の印刷テストでも、良好
な画像が得られた。The developer carrier thus obtained was used in Example 1.
When a test similar to the above was performed, no contamination was found on the contact surface with the latent image holding member in the standing test under high temperature and high humidity, and a good image was obtained in the printing test. Further, a good image was obtained in the printing test after leaving the latent image carrier in pressure contact for 4 weeks.
【0041】[比較例5]吸着剤のアルミナ(住友化学
工業社製:「ALM43」)を配しないこと以外は上記
配合(2)と同様の組成の液状シリコーンゴム原料を用
い、実施例2と同様にして現像剤担持体を得た。得られ
た現像剤担持体の表面硬度は、アスカーC硬度計で68
°であった。[Comparative Example 5] A liquid silicone rubber raw material having the same composition as that of the above-mentioned formulation (2) was used, except that alumina as an adsorbent ("ALM43" manufactured by Sumitomo Chemical Co., Ltd.) was not used. Similarly, a developer carrying member was obtained. The surface hardness of the obtained developer bearing member is 68 by an Asker C hardness meter.
It was °.
【0042】得られた、現像剤担持体につき、実施例1
と同様の試験を行ったところ、高温高湿下での放置テス
トでは、潜像保持体との当接面に明らかな汚染が見ら
れ、また印刷テストではかかる当接部に相当する位置に
画像不良が発生した。The developer carrier thus obtained was used in Example 1.
When the same test was performed, a clear contamination was found on the contact surface with the latent image holder in the storage test under high temperature and high humidity, and in the printing test, the image was found at the position corresponding to the contact part. A defect has occurred.
【0043】[0043]
【発明の効果】以上説明したように、本発明の現像剤担
持体は、電子写真方式や静電記録方式の画像形成装置に
用いた場合、画像形成装置のカラー化や画像品質向上の
ための現像剤の微粒子化、或いは省電力のための現像剤
の低融点化などに拘わらず、現像剤の破壊や固着を使用
時させない程度に低硬度で、かつ低硬度化に伴う汚染物
質のブリードアウトを防止して、潜像保持体や現像剤供
給部材を汚染することなく、良好な画像が確実に得られ
るものである。As described above, when the developer carrying member of the present invention is used in an electrophotographic type or electrostatic recording type image forming apparatus, it is used for colorizing the image forming apparatus and improving the image quality. Despite the fine particles of the developer or the low melting point of the developer to save power, the hardness is low enough not to break or stick the developer when it is used, and bleed-out of contaminants accompanying the low hardness Therefore, a good image can be reliably obtained without contaminating the latent image holding member or the developer supply member.
【図1】本発明にかかる現像剤担持体の一例を示す概略
断面図である。FIG. 1 is a schematic cross-sectional view showing an example of a developer carrying member according to the present invention.
【図2】現像装置の一例を示す概略図である。FIG. 2 is a schematic view showing an example of a developing device.
1 現像剤供給部材 2 現像剤担持体 3 現像剤 4 現像剤量規制ブレード 5 潜像保持体 6 現像剤封止材 7 芯体 8 弾性層 9 被覆層 1 Developer supply member 2 Developer support 3 developer 4 Developer amount control blade 5 Latent image holder 6 Developer sealant 7 core 8 elastic layer 9 coating layer
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) B01J 20/10 B01J 20/10 A D 20/12 20/12 C 20/16 20/16 20/20 20/20 F F16C 13/00 F16C 13/00 B Fターム(参考) 2H077 AC04 AD06 AD13 AD17 FA12 FA22 FA26 FA27 3J103 AA02 AA13 AA14 AA23 BA41 GA02 GA58 GA60 HA03 HA12 HA20 HA53 4G066 AA05B AA16B AA20B AA22B AA30B AA64B AC10C BA26 CA01 FA37 ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 7 Identification code FI theme code (reference) B01J 20/10 B01J 20/10 A D 20/12 20/12 C 20/16 20/16 20/20 20 / 20 F F16C 13/00 F16C 13/00 B F term (reference) 2H077 AC04 AD06 AD13 AD17 FA12 FA22 FA26 FA27 3J103 AA02 AA13 AA14 AA23 BA41 GA02 GA58 GA60 HA03 HA12 HA20 HA53 4G066 AA05B AA16B AA20B30AA22B10A30B AA22B10A30B AA22B10A30A10A30A10A30A30A
Claims (6)
を形成し、これを搬送して潜像保持体表面に形成された
静電潜像に供給し、該静電潜像を現像するための現像剤
担持体において、芯体の外周に少なくとも1層の弾性層
を有し、該弾性層を構成する弾性体中に、比表面積0.
4m2/g以上の吸着剤が該弾性体を形成する高分子物
質成分100重量部に対して0.5〜100重量部の割
合で分散していることを特徴とする現像剤担持体。1. A developer is carried on the surface to form a thin layer of the developer, which is conveyed to be supplied to the electrostatic latent image formed on the surface of the latent image holding member to obtain the electrostatic latent image. In a developer carrying member for developing the toner, at least one elastic layer is provided on the outer periphery of the core, and the elastic body constituting the elastic layer has a specific surface area of 0.
4. A developer carrier, wherein 4 m 2 / g or more of an adsorbent is dispersed in a proportion of 0.5 to 100 parts by weight with respect to 100 parts by weight of a polymeric substance component forming the elastic body.
機ゴム材料である請求項1記載の現像剤担持体。2. The developer carrier according to claim 1, wherein the polymer substance forming the elastic body is an organic rubber material.
リコーンゴム材料である請求項1記載の現像剤担持体。3. The developer carrying member according to claim 1, wherein the polymer substance forming the elastic body is a silicone rubber material.
化物、珪酸塩或いは炭酸塩;珪酸塩活性炭;ゼオライ
ト;酸性白土;シリカ;シリカゲル;シリカ−アルミナ
ゲル;アルミナ;マグネシアから選ばれる1種又は2種
以上である請求項1〜3のいずれか1項に記載の現像剤
担持体。4. The adsorbent is selected from oxides, silicates or carbonates of Mg, Al or Si; silicate activated carbon; zeolite; acid clay; silica; silica gel; silica-alumina gel; alumina; magnesia 1 The developer carrying member according to claim 1, wherein the developer carrying member is one kind or two or more kinds.
は全部が、発泡体で形成された請求項1〜4のいずれか
1項に記載の現像剤担持体。5. The developer carrying member according to claim 1, wherein a part or all of the elastic body layer along the thickness direction is formed of a foam.
像剤担持体を具備してなることを特徴とする現像装置。6. A developing device comprising the developer carrying member according to claim 1. Description:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001245468A JP2003098818A (en) | 2001-07-19 | 2001-08-13 | Developer carrier and developing machine |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001-219179 | 2001-07-19 | ||
| JP2001219179 | 2001-07-19 | ||
| JP2001245468A JP2003098818A (en) | 2001-07-19 | 2001-08-13 | Developer carrier and developing machine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2003098818A true JP2003098818A (en) | 2003-04-04 |
Family
ID=26618978
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001245468A Pending JP2003098818A (en) | 2001-07-19 | 2001-08-13 | Developer carrier and developing machine |
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| Country | Link |
|---|---|
| JP (1) | JP2003098818A (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2008304845A (en) * | 2007-06-11 | 2008-12-18 | Canon Inc | Developing roller having porous inorganic particles adhered thereto, process cartridge for electrophotography, and image forming apparatus for electrophotography |
| JP2010186104A (en) * | 2009-02-13 | 2010-08-26 | Canon Inc | Developing roller, developing method, electrophotographic process cartridge, and electrophotographic image forming apparatus |
| WO2011074610A1 (en) * | 2009-12-15 | 2011-06-23 | 株式会社ブリヂストン | Conductive roller and manufacturing method thereof |
| JP2013200503A (en) * | 2012-03-26 | 2013-10-03 | Fuji Xerox Co Ltd | Charging member, charging device, image forming apparatus, and process cartridge |
-
2001
- 2001-08-13 JP JP2001245468A patent/JP2003098818A/en active Pending
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008304845A (en) * | 2007-06-11 | 2008-12-18 | Canon Inc | Developing roller having porous inorganic particles adhered thereto, process cartridge for electrophotography, and image forming apparatus for electrophotography |
| JP2010186104A (en) * | 2009-02-13 | 2010-08-26 | Canon Inc | Developing roller, developing method, electrophotographic process cartridge, and electrophotographic image forming apparatus |
| WO2011074610A1 (en) * | 2009-12-15 | 2011-06-23 | 株式会社ブリヂストン | Conductive roller and manufacturing method thereof |
| CN102656525A (en) * | 2009-12-15 | 2012-09-05 | 株式会社普利司通 | Conductive roller and manufacturing method thereof |
| CN102656525B (en) * | 2009-12-15 | 2014-10-08 | 株式会社普利司通 | Conductive roller and manufacturing method thereof |
| JP5635012B2 (en) * | 2009-12-15 | 2014-12-03 | 株式会社ブリヂストン | Conductive roller and manufacturing method thereof |
| EP2515180A4 (en) * | 2009-12-15 | 2015-10-14 | Bridgestone Corp | Conductive roller and manufacturing method thereof |
| US9535354B2 (en) | 2009-12-15 | 2017-01-03 | Bridgestone Corporation | Conductive roller and manufacturing method thereof |
| JP2013200503A (en) * | 2012-03-26 | 2013-10-03 | Fuji Xerox Co Ltd | Charging member, charging device, image forming apparatus, and process cartridge |
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