JP2001034062A - Developer carrier and image forming apparatus - Google Patents
Developer carrier and image forming apparatusInfo
- Publication number
- JP2001034062A JP2001034062A JP11205683A JP20568399A JP2001034062A JP 2001034062 A JP2001034062 A JP 2001034062A JP 11205683 A JP11205683 A JP 11205683A JP 20568399 A JP20568399 A JP 20568399A JP 2001034062 A JP2001034062 A JP 2001034062A
- Authority
- JP
- Japan
- Prior art keywords
- developer
- image forming
- developer carrier
- coating layer
- resin
- 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
- 239000011247 coating layer Substances 0.000 claims abstract description 62
- 229920005989 resin Polymers 0.000 claims abstract description 38
- 239000011347 resin Substances 0.000 claims abstract description 38
- 239000010410 layer Substances 0.000 claims abstract description 34
- 239000000843 powder Substances 0.000 claims abstract description 23
- 239000000463 material Substances 0.000 claims abstract description 12
- 239000010409 thin film Substances 0.000 claims abstract description 8
- 239000002904 solvent Substances 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 14
- 230000003746 surface roughness Effects 0.000 claims description 10
- 229920001971 elastomer Polymers 0.000 claims description 8
- 239000005060 rubber Substances 0.000 claims description 8
- 229920000877 Melamine resin Polymers 0.000 claims description 7
- 230000009477 glass transition Effects 0.000 claims description 7
- 229920002050 silicone resin Polymers 0.000 claims description 6
- 229920000178 Acrylic resin Polymers 0.000 claims description 5
- 239000004925 Acrylic resin Substances 0.000 claims description 5
- 239000004640 Melamine resin Substances 0.000 claims description 5
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 5
- 229920000181 Ethylene propylene rubber Polymers 0.000 claims description 4
- 239000002174 Styrene-butadiene Substances 0.000 claims description 4
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 4
- 229920002857 polybutadiene Polymers 0.000 claims description 4
- 229920001225 polyester resin Polymers 0.000 claims description 4
- 239000004645 polyester resin Substances 0.000 claims description 4
- 239000011115 styrene butadiene Substances 0.000 claims description 4
- 239000005062 Polybutadiene Substances 0.000 claims description 3
- 229920006311 Urethane elastomer Polymers 0.000 claims description 3
- 239000013013 elastic material Substances 0.000 claims description 3
- 230000007774 longterm Effects 0.000 abstract description 9
- 239000011248 coating agent Substances 0.000 description 30
- 238000000576 coating method Methods 0.000 description 30
- 239000007788 liquid Substances 0.000 description 18
- 239000000203 mixture Substances 0.000 description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 12
- 239000006258 conductive agent Substances 0.000 description 11
- 239000007787 solid Substances 0.000 description 9
- 238000011161 development Methods 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- 239000010408 film Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 235000019241 carbon black Nutrition 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- -1 borofluoride Chemical compound 0.000 description 5
- 239000006229 carbon black Substances 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 230000007547 defect Effects 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 5
- 229910001887 tin oxide Inorganic materials 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 229920000180 alkyd Polymers 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 239000005011 phenolic resin Substances 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 239000005453 ketone based solvent Substances 0.000 description 3
- 238000005065 mining Methods 0.000 description 3
- 239000012046 mixed solvent Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 108091008695 photoreceptors Proteins 0.000 description 3
- 229920006122 polyamide resin Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical class C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical group CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000011354 acetal resin Substances 0.000 description 2
- 239000006230 acetylene black Substances 0.000 description 2
- 229920006243 acrylic copolymer Polymers 0.000 description 2
- 125000004849 alkoxymethyl group Chemical group 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- VICYBMUVWHJEFT-UHFFFAOYSA-N dodecyltrimethylammonium ion Chemical compound CCCCCCCCCCCC[N+](C)(C)C VICYBMUVWHJEFT-UHFFFAOYSA-N 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920006324 polyoxymethylene Polymers 0.000 description 2
- 229920003225 polyurethane elastomer Polymers 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 229920002379 silicone rubber Polymers 0.000 description 2
- 239000004945 silicone rubber Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- PDSVZUAJOIQXRK-UHFFFAOYSA-N trimethyl(octadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)C PDSVZUAJOIQXRK-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical class [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 101100287595 Caenorhabditis elegans kin-2 gene Proteins 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-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
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920001744 Polyaldehyde Chemical class 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- JMMMQMYUUHNYPO-UHFFFAOYSA-N [amino(isocyanato)hydrazinylidene]-oxomethane Chemical compound O=C=NN(N)N=C=O JMMMQMYUUHNYPO-UHFFFAOYSA-N 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000004018 acid anhydride group Chemical group 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 125000003172 aldehyde group Chemical group 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 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
- 125000005370 alkoxysilyl group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 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
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-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
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- RLGQACBPNDBWTB-UHFFFAOYSA-N cetyltrimethylammonium ion Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)C RLGQACBPNDBWTB-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 239000002482 conductive additive Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 239000012024 dehydrating agents Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000007606 doctor blade method Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 229920005558 epichlorohydrin rubber Polymers 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- ICIWUVCWSCSTAQ-UHFFFAOYSA-M iodate Chemical compound [O-]I(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-M 0.000 description 1
- 235000013675 iodine Nutrition 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- 239000003273 ketjen black Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- DAZXVJBJRMWXJP-UHFFFAOYSA-N n,n-dimethylethylamine Chemical compound CCN(C)C DAZXVJBJRMWXJP-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- BMGNSKKZFQMGDH-FDGPNNRMSA-L nickel(2+);(z)-4-oxopent-2-en-2-olate Chemical compound [Ni+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O BMGNSKKZFQMGDH-FDGPNNRMSA-L 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000768 polyamine Chemical class 0.000 description 1
- 229920001228 polyisocyanate Chemical class 0.000 description 1
- 239000005056 polyisocyanate Chemical class 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000002296 pyrolytic carbon Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000013517 stratification Methods 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000002345 surface coating layer Substances 0.000 description 1
- 238000012360 testing method Methods 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
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- PPPHYGCRGMTZNA-UHFFFAOYSA-M trifluoromethyl sulfate Chemical compound [O-]S(=O)(=O)OC(F)(F)F PPPHYGCRGMTZNA-UHFFFAOYSA-M 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Dry Development In Electrophotography (AREA)
- Rolls And Other Rotary Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
(57)【要約】
【課題】 長期耐久性に優れ、かつ高品質の画像を形成
し得る現像剤担持体を提供すること。
【解決手段】 表面に現像剤を担持してその薄膜を形成
し、この状態で画像形成体に接触又は近接して、該画像
形成体表面に該現像剤を供給することにより、画像形成
体表面に可視画像を形成させる現像剤担持体において、
現像剤担持体が、導電性弾性層の表面に、樹脂100重
量部及び70重量部を超え200重量部以下の100 〜
105 Ω・cmの導電性粉体を含有する材料からなる被
覆層を有するものである現像剤担持体、及びこの現像剤
担持体を装着した画像形成装置である。
(57) [Problem] To provide a developer carrier excellent in long-term durability and capable of forming a high-quality image. SOLUTION: The developer is carried on the surface to form a thin film thereof, and in this state, the developer is supplied to the surface of the image forming body by contacting or approaching the image forming body, whereby the surface of the image forming body is supplied. In a developer carrier for forming a visible image on the
Developer carrying member, the surface of the conductive elastic layer, the resin 100 parts by weight and 70 parts by weight of more than 200 parts by weight or less of 10 0 -
A developer carrier having a coating layer made of a material containing a conductive powder of 10 5 Ω · cm, and an image forming apparatus equipped with the developer carrier.
Description
【0001】[0001]
【発明の属する技術分野】本発明は、現像剤担持体及び
画像形成装置に関し、さらに詳しくは、複写機、ファク
シミリ、プリンター等の画像形成装置において、静電潜
像を保持した感光体や紙等の画像形成体に現像剤を供給
して、該画像形成体表面に可視像を形成させるための現
像剤担持体であって、画像むらのない高品質の画像を与
え、かつ長期使用における特性変化が小さく耐久性に優
れた現像剤担持体、及びそれを装着した画像形成装置に
関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a developer carrier and an image forming apparatus, and more particularly, to an image forming apparatus such as a copying machine, a facsimile, a printer, and the like. A developer carrying member for supplying a developer to the image forming body to form a visible image on the surface of the image forming body, providing a high-quality image without image unevenness, and a characteristic in long-term use. The present invention relates to a developer carrier having small changes and excellent durability, and an image forming apparatus equipped with the same.
【0002】[0002]
【従来の技術】従来、複写機やプリンター等の電子写真
方式の画像形成装置などにおいて、静電潜像を保持した
感光体等の画像形成体に一成分トナー(現像剤)を供給
し、該トナーを潜像に付着させて可視化する画像形成方
法として、加圧現像法が知られている(米国特許第31
52012号明細書、同第3731146号明細書
等)。この加圧現像法は、トナーを担持したトナー担持
体(現像剤担持体)を、静電潜像を保持した画像形成体
(感光体)に接触させて、トナーを該画像形成体の潜像
に付着させることにより画像形成を行うもので、このた
め上記トナー担持体を導電性と弾性を有する導電性弾性
体で形成することが必要である。すなわち、この加圧現
像法では、例えば図2に示すように、トナーを供給する
ためのトナー塗布用ローラ5と静電潜像を保持した画像
形成体(感光体)6との間に、トナー担持体(現像ロー
ラ)1が配設され、これらトナー担持体1、画像形成体
6及びトナー塗布用ローラ5がそれぞれ図中矢印方向に
回転することにより、トナー7がトナー塗布用ローラ5
によりトナー担持体1の表面に供給され、このトナーが
成層ブレード8により均一な薄膜に整えられる。そし
て、この状態でトナー担持体1が画像形成体6と接触し
ながら回転することにより、薄層に形成されたトナーが
トナー担持体1から画像形成体6の潜像に付着して、該
潜像が可視化するようになっている。図中9は転写部で
あり、ここで紙等の記録媒体にトナー画像を転写するよ
うになっている。また、10はクリーニング部であり、
そのクリーニングブレード11により転写後に画像形成
体6表面に残存するトナーを除去するようになってい
る。2. Description of the Related Art Conventionally, in an electrophotographic image forming apparatus such as a copying machine or a printer, a one-component toner (developer) is supplied to an image forming body such as a photoconductor holding an electrostatic latent image. A pressure development method is known as an image forming method for visualizing toner by attaching toner to a latent image (US Pat.
No. 52012, No. 3731146, etc.). In this pressure development method, a toner carrier (developer carrier) carrying a toner is brought into contact with an image forming body (photoreceptor) holding an electrostatic latent image, and the toner is transferred to the latent image of the image forming body. The toner carrier is formed of a conductive elastic material having conductivity and elasticity. That is, in this pressure development method, as shown in FIG. 2, for example, a toner is applied between a toner applying roller 5 for supplying toner and an image forming body (photoconductor) 6 holding an electrostatic latent image. A carrier (development roller) 1 is disposed, and the toner 7 is rotated by the toner carrier 1, the image forming body 6, and the toner application roller 5 in the direction of the arrow in FIG.
Is supplied to the surface of the toner carrier 1, and the toner is formed into a uniform thin film by the layering blade 8. Then, in this state, when the toner carrier 1 rotates while being in contact with the image forming body 6, the toner formed in a thin layer adheres from the toner carrier 1 to the latent image of the image forming body 6, and The image is made visible. In the drawing, reference numeral 9 denotes a transfer unit, which transfers a toner image to a recording medium such as paper. Reference numeral 10 denotes a cleaning unit,
The cleaning blade 11 removes the toner remaining on the surface of the image forming body 6 after the transfer.
【0003】このような加圧現像法による画像形成装置
においては、トナー担持体1は、画像形成体6に密着し
た状態を保持しながら回転しなければならず、このた
め、図1の概略断面図に示すように、金属等の良導電性
材料からなるシャフト2の外周に、シリコーンゴム,ア
クリロニトリルブタジエンゴム,エチレンプロピレンゴ
ム,ポリウレタンゴム等の弾性ゴムやフォームなどに導
電剤を配合して導電性を付与した導電性弾性体からなる
導電性弾性層3を形成した構造となっている。さらに、
トナー7に対する帯電性や付着性の制御のために、画像
形成体6及び成層ブレード8との摩擦力制御のために、
あるいは弾性体による画像形成体の汚染防止などのため
に、樹脂等からなる被覆層4が導電性弾性層3の表面に
設けられている。一方、紙やOHP用紙などの紙葉類か
らなる画像形成体に、トナー担持体上に担持させたトナ
ーを孔状の制御電極を介して直線飛翔せしめて、画像を
形成させる画像形成法も提案されている。また、画像形
成体(感光体)に近接して非接触状態に配設されたスリ
ーブ状のトナー担持体の表面に、薄層に成層した非磁性
トナーを担持し、これを画像形成体上に飛翔させて現像
を行い、画像を形成させる方法も提案されている(特開
昭58−116559号公報)。In such an image forming apparatus using the pressure development method, the toner carrier 1 must rotate while maintaining a state in which the toner carrier 1 is in close contact with the image forming body 6. As shown in the figure, a conductive agent is blended with an elastic rubber or foam such as silicone rubber, acrylonitrile butadiene rubber, ethylene propylene rubber, polyurethane rubber, etc. around the outer periphery of the shaft 2 made of a good conductive material such as metal. The structure is such that a conductive elastic layer 3 made of a conductive elastic body provided with is formed. further,
To control the chargeability and adhesion of the toner 7, and to control the frictional force between the image forming body 6 and the layering blade 8,
Alternatively, a coating layer 4 made of a resin or the like is provided on the surface of the conductive elastic layer 3 in order to prevent contamination of the image forming body by the elastic body. On the other hand, an image forming method for forming an image by causing a toner carried on a toner carrier to fly in a straight line through an aperture-shaped control electrode on an image forming body made of paper such as paper or OHP paper is also proposed. Have been. Also, a thin layer of non-magnetic toner is carried on the surface of a sleeve-shaped toner carrier disposed in a non-contact state close to the image forming body (photoreceptor), and this is placed on the image forming body. A method of forming an image by developing by flying is also proposed (JP-A-58-116559).
【0004】いずれの場合も、トナー担持体上には、ト
ナーに対する帯電性や付着性の制御のために、あるいは
画像形成体,成層ブレード,制御電極等の他の部材との
摩擦力低減などのために、樹脂等からなる被覆層が導電
性弾性層の表面に設けられている。ところで、現像剤担
持体は、現像剤担持体上に保持した現像剤を画像形成体
に移行させる推進力となるバイアス電圧を得るために、
現像担持体全体の抵抗値は106 〜1011Ω程度となっ
ている。そして多くの場合、抵抗の調整を容易にするた
めに、導電性弾性層の固有抵抗を低抵抗とし、樹脂から
なる被覆層の固有抵抗を高抵抗としている。その際、被
覆層の固有抵抗の調整は、被覆層を形成する樹脂にカー
ボンや金属酸化物等の導電性粉体を含有せしめることに
より行っている。本発明者らは、これまでに、メラミン
樹脂,フェノール樹脂,アルキッド樹脂,フッ素樹脂,
ポリアミド樹脂等の樹脂を被覆層に用いた現像剤担持体
を、摩擦や画像を改良し得る現像剤担持体として提案し
てきた。[0004] In any case, the toner carrier is provided on the toner carrier for controlling the chargeability and adhesion of the toner or for reducing the frictional force with other members such as an image forming body, a layered blade, and a control electrode. To this end, a coating layer made of a resin or the like is provided on the surface of the conductive elastic layer. By the way, in order to obtain a bias voltage which is a driving force for transferring the developer held on the developer carrier to the image forming body,
The resistance value of the entire development carrier is about 10 6 to 10 11 Ω. In many cases, in order to easily adjust the resistance, the specific resistance of the conductive elastic layer is set to be low, and the specific resistance of the coating layer made of resin is set to be high. At this time, the adjustment of the specific resistance of the coating layer is performed by adding a conductive powder such as carbon or metal oxide to the resin forming the coating layer. The present inventors have previously developed melamine resins, phenol resins, alkyd resins, fluororesins,
A developer carrier using a resin such as a polyamide resin for the coating layer has been proposed as a developer carrier capable of improving friction and an image.
【0005】[0005]
【発明が解決しようとする課題】しかしながら、最近に
至って、プリンターなどが高速化されたり、微細画像が
要求されたり、あるいはカラー画像化されたりすること
により、画像形成に対する要求が厳しくなり、従来の現
像剤担持体では対応できない種々の問題が顕在化してき
た。すなわち、現像剤担持体をプリンターなどに組み込
み、長期間使用し、印刷枚数が増加した場合、白地画像
において画像のかぶりが発生し、黒画像において濃度低
下ムラが発生するなどの問題が顕在化してきた。本発明
は、上記事情に鑑みてなされたもので、長期間使用して
も白地画像におけるかぶり、黒画像における濃度低下ム
ラなどの画像不良が発生しない、耐久性に優れた現像剤
担持体及びそれを装着した画像形成装置を提供すること
を目的とするものである。However, recently, the demand for image formation has become strict due to the speeding up of printers and the like, the demand for fine images, and the development of color images. Various problems that cannot be dealt with by the developer carrier have become apparent. In other words, when the developer carrier is incorporated in a printer or the like and used for a long period of time and the number of printed sheets increases, problems such as image fogging in a white background image and unevenness in density reduction in a black image become apparent. Was. The present invention has been made in view of the above circumstances, and does not cause image defects such as fog on a white background image and uneven density reduction in a black image even when used for a long period of time. It is an object of the present invention to provide an image forming apparatus equipped with a.
【0006】[0006]
【課題を解決するための手段】本発明者らは、長期耐久
性に優れ、かつ高品質の画像を形成し得る現像剤担持体
について鋭意研究を行った結果、下記の知見を得た。す
なわち、上述した白地画像のかぶりや黒画像の濃度低下
ムラは、現像剤担持体を長期使用した場合に、現像剤担
持体と、現像剤、現像剤塗布用ローラあるいは成層ブレ
ード等との摩擦により、現像剤担持体表面被覆層が摩耗
したり、被覆層表面に多量の現像剤フィルミングが生じ
たりし、その結果、現像剤担持体の表面が変化して、現
像剤の帯電量が低下することにより発生することを見出
した。そして、本発明者らは、さらに研究を進めた結
果、導電性弾性層の表面に、特定範囲の固有抵抗を有す
る導電性粉体を適量含有する樹脂からなる被覆層を設け
た現像剤担持体が、長期耐久性に優れ、かつ高品質の画
像を形成し得ることを見出した。本発明は、かかる知見
に基づいて完成したものである。すなわち、本発明は、
表面に現像剤を担持してその薄膜を形成し、この状態で
画像形成体に接触又は近接して、該画像形成体表面に該
現像剤を供給することにより、画像形成体表面に可視画
像を形成させる現像剤担持体において、現像剤担持体
が、導電性弾性層の表面に、樹脂100重量部及び70
重量部を超え200重量部以下の100 〜105 Ω・c
mの導電性粉体を含有する材料からなる被覆層を有する
ものであることを特徴とする現像剤担持体を提供するも
のである。また、本発明は、現像剤担持体が装着されて
なり、かつ現像剤担持体の表面に現像剤を担持してその
薄膜を形成し、この現像剤担持体を画像形成体に接触又
は近接させて、該画像形成体表面に現像剤を供給するこ
とにより、画像形成体表面に可視画像を形成させる画像
形成装置において、現像剤担持体として、上記現像剤担
持体を用いたことを特徴とする画像形成装置を提供する
ものである。Means for Solving the Problems The present inventors have conducted intensive studies on a developer carrying member which is excellent in long-term durability and can form a high-quality image, and as a result, has obtained the following knowledge. That is, the fogging of the white background image and the density unevenness of the black image are caused by friction between the developer carrier and the developer, the developer application roller or the laminating blade when the developer carrier is used for a long time. In addition, the developer carrier surface coating layer is worn out, and a large amount of developer filming occurs on the surface of the coating layer. As a result, the surface of the developer carrier changes, and the charge amount of the developer decreases. It has been found that this can occur. As a result of further research, the present inventors have found that a developer carrier having a coating layer made of a resin containing an appropriate amount of conductive powder having a specific range of specific resistance is provided on the surface of the conductive elastic layer. However, it was found that it was possible to form a high quality image with excellent long-term durability. The present invention has been completed based on such findings. That is, the present invention
A developer is supported on the surface to form a thin film, and in this state, the visible image is formed on the surface of the image forming body by supplying the developer to the surface of the image forming body by contacting or approaching the image forming body. In the developer carrier to be formed, 100 parts by weight of the resin and 70 parts by weight of the
Of 200 parts by weight or less than the weight part 10 0 ~10 5 Ω · c
a developer carrying member having a coating layer made of a material containing a conductive powder of m. Further, the present invention provides a method in which a developer carrier is mounted, and a developer is carried on the surface of the developer carrier to form a thin film of the developer, and the developer carrier is brought into contact with or close to the image forming body. An image forming apparatus that forms a visible image on the surface of the image forming body by supplying a developer to the surface of the image forming body, wherein the developer supporting body is used as the developer supporting body. An image forming apparatus is provided.
【0007】[0007]
【発明の実施の形態】本発明の現像剤担持体は、図1に
示すように、良導電性シャフト2の外周に導電性弾性層
3が形成され、導電性弾性層3の表面に被覆層4を形成
したものである。シャフト2としては、良好な導電性を
有するものであればいずれのものも使用し得るが、通常
は、金属製の中実体からなる芯金や内部を中空にくりぬ
いた金属製円筒体等の金属製シャフトが用いられる。上
記導電性弾性層3には、適当なゴム材料に導電剤を添加
して導電性を付与した弾性材料が用いられる。ここで、
ゴム材料としては、特に制限はなく、例えばニトリルゴ
ム,エチレンプロピレンゴム,エチレンプロピレンジエ
ンゴム,スチレンブタジエンゴム,ブタジエンゴム,イ
ソプレンゴム,天然ゴム,シリコーンゴム,ウレタンゴ
ム,アクリルゴム,クロロプレンゴム,ブチルゴム,エ
ピクロルヒドリンゴム等が挙げられ、これらは一種用い
てもよく、二種以上を組み合わせて用いることができる
が、これらの中で、特にブタジエンゴム,エチレンプロ
ピレンゴム及びウレタンゴムから選ばれる一種又は二種
以上の混合物が好ましい。DESCRIPTION OF THE PREFERRED EMBODIMENTS As shown in FIG. 1, a developer carrier of the present invention has a conductive elastic layer 3 formed on the outer periphery of a good conductive shaft 2 and a coating layer formed on the surface of the conductive elastic layer 3. 4 is formed. As the shaft 2, any material having good conductivity can be used, but usually, a metal such as a metal core bar made of a solid metal body or a metal cylindrical body having a hollow inside is used. A shaft made of is used. The conductive elastic layer 3 is made of an elastic material obtained by adding a conductive agent to an appropriate rubber material to impart conductivity. here,
There is no particular limitation on the rubber material. For example, nitrile rubber, ethylene propylene rubber, ethylene propylene diene rubber, styrene butadiene rubber, butadiene rubber, isoprene rubber, natural rubber, silicone rubber, urethane rubber, acrylic rubber, chloroprene rubber, butyl rubber, Epichlorohydrin rubber and the like may be used, and these may be used alone or in combination of two or more. Among them, one or more selected from among butadiene rubber, ethylene propylene rubber and urethane rubber are particularly preferred. Are preferred.
【0008】一方、これらのゴム材料に添加される導電
剤は、イオン導電剤と電子導電剤とがあり、前者のイオ
ン導電剤の例としては、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
ウム等の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,ステアリルトリメチルアン
ミニウム等のオクタ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,変性脂肪族ジメチルエ
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,
アルキル硫酸塩,カルボン酸塩,スルホン酸塩などのア
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又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
ホン酸塩などが挙げられる。また、電子導電剤の例とし
ては、ケッチェンブラック,アセチレンブラック等の導
電性カーボンブラック;SAF,ISAF,HAF,F
EF,GPF,SRF,FT,MT等のゴム用カーボン
ブラック;酸化処理を施したインク用カーボンブラッ
ク,熱分解カーボンブラック,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,銅等の金属などの粉末が挙げられる。On the other hand, conductive agents added to these rubber materials include an ionic conductive agent and an electronic conductive agent. Examples of the former ionic conductive agent include tetraethylammonium, tetrabutylammonium, lauryltrimethylammonium and the like. Perchlorate, chlorate, hydrochloride, such as octadecyltrimethylammonium, benzyltrimethylammonium, modified aliphatic dimethylethylammonium, such as dodecyltrimethylammonium, hexadecyltrimethylammonium, stearyltrimethylammonium;
Bromate, iodate, borofluoride, sulfate,
Ammonium salts such as alkyl sulfates, carboxylates, and sulfonates; perchlorates, chlorates, hydrochlorides, bromates, and iodines of alkali metals or alkaline earth metals such as lithium, sodium, calcium, and magnesium Acid salt,
Borofluoride, trifluoromethyl sulfate, sulfonate and the like can be mentioned. Examples of the electronic conductive agent include conductive carbon blacks such as Ketjen black and acetylene black; SAF, ISAF, HAF, F
Carbon black for rubber such as EF, GPF, SRF, FT, and MT; carbon black for ink after oxidation treatment, pyrolytic carbon black, graphite; conductive metal oxide such as tin oxide, titanium oxide, and zinc oxide; nickel And powders of metals such as copper.
【0009】これらの導電剤は一種用いてもよく、二種
以上を組み合わせて用いてもよい。また、その添加量は
特に制限されるものではないが、イオン導電剤の場合、
上記ゴム材料100重量部に対して、0.01〜5重量
部、好ましくは0.05〜2重量部の範囲とすることがで
き、電子導電剤の場合、1〜50重量部、好ましくは5
〜40重量部の範囲とすることができる。この導電剤添
加量の調整により、導電性弾性層の固有抵抗値を、10
3 〜10 12Ω・cm、特に104 〜108 Ω・cmの範
囲に調整するのが好ましい。なお、この導電性弾性層に
は、上記導電剤以外に必要に応じ、従来公知の充填剤,
架橋剤など、その他のゴム用添加剤を適宜添加すること
ができる。この導電性弾性層の硬度は、アスカーC型で
40〜80°、特に50〜75°の範囲とすることが好
ましい。この硬度が80°を超えると現像剤担持体が硬
くなり、画像形成等との接触面積が小さくなって、良好
な画像形成が行えなくなる恐れがある上、現像剤に損傷
を与えて画像形成体や成層ブレードへのトナー固着など
が発生して、画像不良が生じる原因となる。逆に低硬度
になりすぎると、画像形成体や成層ブレードとの摩擦が
大きくなり、ジッター等の画像不良が発生する恐れがあ
る。These conductive agents may be used alone,
You may use it combining the above. The amount of addition
Although not particularly limited, in the case of an ion conductive agent,
0.01 to 5 parts by weight based on 100 parts by weight of the rubber material
Parts, preferably in the range of 0.05 to 2 parts by weight.
1 to 50 parts by weight, preferably 5
It can be in the range of 4040 parts by weight. This conductive additive
By adjusting the addition amount, the specific resistance of the conductive elastic layer is reduced to 10
Three-10 12Ω · cm, especially 10Four-108Ω ・ cm range
It is preferable to adjust to the surroundings. In addition, this conductive elastic layer
May be a conventionally known filler, if necessary, in addition to the conductive agent.
Add other rubber additives, such as crosslinking agents, as appropriate
Can be. This conductive elastic layer has a hardness of Asker C type.
The angle is preferably in the range of 40 to 80 °, especially 50 to 75 °.
Good. When the hardness exceeds 80 °, the developer carrier becomes hard.
And the contact area with image formation etc. becomes smaller,
Image formation may not be possible and the developer may be damaged.
To fix toner on the image forming body or layering blade
Occurs, which causes image defects. Conversely, low hardness
If it becomes too high, friction with the image forming body and
Large, and image defects such as jitter may occur.
You.
【0010】導電性弾性層は、画像形成体や成層ブレー
ド等と当接して使用されることから、圧縮永久歪みが小
さいことが好ましく、具体的には20%以下、特に10
%以下が好ましい。特にポリウレタンゴムは、この圧縮
永久歪みを小さく設計できるので、特に好ましい。ま
た、この導電性弾性層の表面粗さは、JIS10点平均
粗さで、15μmRz以下、特に3〜10μmRzとす
ることが好ましい。この平均粗さが15μmRzを超え
ると現像剤担持体の表面を形成する被覆層を厚く形成す
る必要があり、その結果、現像剤担持体表面が硬くな
り、現像剤に損傷を与えて画像形成体や成層ブレードへ
の現像剤固着などが発生して、画像不良となるので好ま
しくない。また、Rzが小さすぎると該被覆層を形成し
たときに、現像剤担持体の表面のRzが小さくなりす
ぎ、現像剤担持量が少なくなり画像濃度が低下する恐れ
が生じる。なお、この表面粗さは、表面粗さ計「サーフ
コム590A」(東京精密社製)を用いて、円周方向に
測定長さ2.4mm、測定速さ0.3mm/秒、カットオフ
波長0.8mmでローラのシャフト方向及び円周方向で偏
りがないように300箇所以上測定して求めた値である
(以下においても同様)。Since the conductive elastic layer is used in contact with an image forming body, a layered blade or the like, it is preferable that the compression set is small, specifically, 20% or less, particularly 10% or less.
% Or less is preferable. In particular, polyurethane rubber is particularly preferable because the compression set can be designed to be small. The surface roughness of the conductive elastic layer is preferably 15 μmRz or less, particularly preferably 3 to 10 μmRz in terms of JIS 10-point average roughness. If the average roughness exceeds 15 μmRz, it is necessary to form a thick coating layer forming the surface of the developer carrying member, and as a result, the surface of the developer carrying member becomes hard and damages the developer, resulting in an image forming member. And the developer adheres to the stratification blade, which results in image failure, which is not preferable. On the other hand, if the Rz is too small, when the coating layer is formed, the Rz on the surface of the developer carrying member becomes too small, and the amount of the developer carried becomes small, so that the image density may be reduced. The surface roughness was measured using a surface roughness meter “Surfcom 590A” (manufactured by Tokyo Seimitsu Co., Ltd.) in the circumferential direction at a measurement length of 2.4 mm, a measurement speed of 0.3 mm / sec, and a cutoff wavelength of 0 mm. It is a value obtained by measuring 300 points or more at 0.8 mm so that there is no deviation in the shaft direction and circumferential direction of the roller (the same applies to the following).
【0011】本発明の現像剤担持体においては、現像剤
に対する帯電性や付着性の制御のために、画像形成体や
成層ブレードなどとの摩擦力低減のために、あるいは、
弾性体による画像形成体の汚染防止などのために、上記
導電性弾性層の表面に樹脂等からなる被覆層が設けられ
ている。この被覆層は、ガラス転移点が10℃以下の樹
脂を含有する材料で形成することが好ましく、この樹脂
のガラス転移点は−50〜0℃であることが特に好まし
い。ガラス転移点が10℃を超え40℃以下の樹脂を用
いると、使用環境温度によって被覆層の物理的特性が大
きく変化し、現像剤の搬送量及び帯電量がばらついてし
まう恐れがある。また、ガラス転移点が40℃を超える
樹脂を用いると、被覆層が脆くなるため、導電性弾性層
の変形に追従することができず、このため被覆層が割れ
やすくなる。また、被覆層の動的弾性率E’は107 〜
109.8 dyn/cm2 であることが好ましく、特に好
ましくは108 〜109.6 dyn/cm2 である。被覆
層の損失正接tanδは0.7以下であることが好まし
く、特に好ましくは0.05〜0.5である。ここで、損失
正接tanδとは、(サンプルに応力を与えた際の)動
的弾性率E’に対する動的損失E”の比をいう。被覆層
の動的弾性率E’が107 〜109.8 dyn/cm
2 で、かつ損失正接tanδが0.7以下であると、耐久
印刷時に現像剤のフィルミングや被覆層の割れが発生せ
ず、現像剤担持体を長期間使用した場合に、白地画像に
おける画像のかぶりを防止することができ、黒ベタ画像
において濃度不足が生じることなく、かつ画像ノイズの
発生を防止することができる。In the developer carrying member of the present invention, in order to control the chargeability and adhesion of the developer, to reduce the frictional force with an image forming member, a layered blade, or the like, or
In order to prevent the image forming body from being contaminated by the elastic body, a coating layer made of a resin or the like is provided on the surface of the conductive elastic layer. This coating layer is preferably formed of a material containing a resin having a glass transition point of 10 ° C. or lower, and the resin preferably has a glass transition point of −50 to 0 ° C. When a resin having a glass transition point of more than 10 ° C. and 40 ° C. or less is used, the physical properties of the coating layer greatly change depending on the use environment temperature, and there is a possibility that the transport amount and charge amount of the developer may vary. When a resin having a glass transition point exceeding 40 ° C. is used, the coating layer becomes brittle, so that it cannot follow the deformation of the conductive elastic layer, and thus the coating layer is easily broken. The dynamic elastic modulus E ′ of the coating layer is 10 7 to
It is preferably 10 9.8 dyn / cm 2 , particularly preferably 10 8 to 109.6 dyn / cm 2 . The loss tangent tan δ of the coating layer is preferably 0.7 or less, particularly preferably 0.05 to 0.5. Here, the loss tangent tan δ refers to the ratio of the dynamic loss E ″ to the dynamic elastic modulus E ′ (when stress is applied to the sample). The dynamic elastic modulus E ′ of the coating layer is 10 7 to 10. 9.8 dyn / cm
2 , and the loss tangent tan δ is 0.7 or less, no filming of the developer or cracking of the coating layer occurs during the durable printing, and the image on the white background image is obtained when the developer carrier is used for a long time. Fogging can be prevented, and the occurrence of image noise can be prevented without causing insufficient density in a solid black image.
【0012】本発明に係る被覆層の形成に用いる樹脂と
しては、架橋性樹脂等が挙げられる。ここで、架橋性樹
脂とは、熱,触媒,空気(酸素),湿気(水),電子線
などにより自己架橋する樹脂あるいは架橋剤や他の架橋
性樹脂との反応により架橋する樹脂をいう。このような
架橋性樹脂の例としては、水酸基,カルボキシル基,酸
無水物基,アミノ基,イミノ基,イソシアネート基,メ
チロール基,アルコキシメチル基,アルデヒド基,メル
カプト基,エポキシ基,不飽和基等の反応基を持つフッ
素樹脂,ポリアミド樹脂,アクリルウレタン樹脂,アル
キッド樹脂,フェノール樹脂,メラミン樹脂,シリコー
ン樹脂,ウレタン樹脂,ポリエステル樹脂,ポリビニル
アセタール樹脂,エポキシ樹脂,ポリエーテル樹脂,ア
ミノ樹脂,尿素樹脂,アクリル樹脂,アクリル変性シリ
コーン樹脂,スチレンブタジエン樹脂等及びこれらの混
合物が挙げられる。これらの中で、フッ素樹脂,ポリア
ミド樹脂,アクリルウレタン樹脂,アルキッド樹脂,フ
ェノール樹脂,メラミン樹脂,シリコーン樹脂,ウレタ
ン樹脂,ポリエステル樹脂,ポリビニルアセタール樹
脂,エポキシ樹脂,アクリル樹脂,アクリル変性シリコ
ーン樹脂,スチレンブタジエン樹脂及びこれらの混合物
が好ましく、特にアルキッド樹脂,フェノール樹脂,メ
ラミン樹脂,ポリエステル樹脂,アクリル樹脂,アクリ
ル変性シリコーン樹脂,スチレンブタジエン樹脂及びこ
れらの混合物が、現像剤の帯電能、現像剤に対する非汚
染性、他の部材との摩擦力低減、画像形成体に対する非
汚染性などの点から好適である。The resin used for forming the coating layer according to the present invention includes a crosslinkable resin. Here, the crosslinkable resin refers to a resin that is self-crosslinked by heat, a catalyst, air (oxygen), moisture (water), an electron beam, or the like, or a resin that is crosslinked by a reaction with a crosslinking agent or another crosslinkable resin. Examples of such crosslinkable resins include hydroxyl, carboxyl, acid anhydride, amino, imino, isocyanate, methylol, alkoxymethyl, aldehyde, mercapto, epoxy, and unsaturated groups. Resin, polyamide resin, acrylic urethane resin, alkyd resin, phenol resin, melamine resin, silicone resin, urethane resin, polyester resin, polyvinyl acetal resin, epoxy resin, polyether resin, amino resin, urea resin Acrylic resins, acrylic-modified silicone resins, styrene-butadiene resins, and the like, and mixtures thereof, may be used. Among them, fluorine resin, polyamide resin, acrylic urethane resin, alkyd resin, phenol resin, melamine resin, silicone resin, urethane resin, polyester resin, polyvinyl acetal resin, epoxy resin, acrylic resin, acrylic modified silicone resin, styrene butadiene Resins and mixtures thereof are preferred. Particularly, alkyd resins, phenol resins, melamine resins, polyester resins, acrylic resins, acryl-modified silicone resins, styrene-butadiene resins and mixtures thereof are suitable for the chargeability of the developer and the non-staining property to the developer. This is preferable from the viewpoints of reduction in frictional force with other members, non-contamination of the image forming body, and the like.
【0013】上記触媒としては、例えば過酸化物やアゾ
化合物などのラジカル触媒,酸触媒,塩基性触媒などが
挙げられる。また、上記架橋剤としては、は水酸基,カ
ルボキシル基,酸無水物基,アミノ基,イミノ基,イソ
シアネート基,メチロール基,アルコキシメチル基,ア
ルデヒド基,メルカプト基,エポキシ基,不飽和基等の
反応基を1分子中に2個以上もつ分子量1000以下の
化合物、好ましくは分子量500以下の化合物であり、
例えば、ポリオール化合物,ポリイソシアネート化合
物,ポリアルデヒド化合物,ポリアミン化合物,ポリエ
ポキシ化合物等が挙げられる。本発明に係る被覆層は、
溶剤に対する不溶率が70重量%以上のものが好まし
く、この不溶率が70重量%未満では、長期間の放置に
より、画像形成体や成層ブレードなど、トナー担持体と
接触している部材の圧接痕ができ、その結果、画像に黒
横線などの不具合が生じる恐れがある。特に、溶剤不溶
率が80重量%以上のものが好適である。Examples of the catalyst include radical catalysts such as peroxides and azo compounds, acid catalysts, and basic catalysts. Examples of the crosslinking agent include a hydroxyl group, a carboxyl group, an acid anhydride group, an amino group, an imino group, an isocyanate group, a methylol group, an alkoxymethyl group, an aldehyde group, a mercapto group, an epoxy group, and an unsaturated group. A compound having a molecular weight of 1,000 or less having two or more groups in one molecule, preferably a compound having a molecular weight of 500 or less,
For example, polyol compounds, polyisocyanate compounds, polyaldehyde compounds, polyamine compounds, polyepoxy compounds and the like can be mentioned. The coating layer according to the present invention,
A solvent having an insolubility of 70% by weight or more is preferable. If the insolubility is less than 70% by weight, a contact mark of a member which is in contact with a toner carrier, such as an image forming member or a layered blade, after being left for a long period of time. As a result, a problem such as a horizontal black line may occur in the image. Particularly, those having a solvent insolubility of 80% by weight or more are preferable.
【0014】本発明に係る被覆層は、上記架橋性樹脂等
を主成分とするものであるが、その他に、現像剤への帯
電能のさらなる向上、他の部材との摩擦力低減や導電性
付与等の目的で、荷電制御剤,滑材,導電剤、その他の
樹脂等の種々の添加剤を含有させることができる。本発
明の現像剤担持体においては、このような被覆層の抵抗
を、導電性弾性層の抵抗より高くすることが、現像剤担
持体の抵抗を調整する上で好ましく、この被覆層の好ま
しい固有抵抗値は107 〜1016Ω・cmの範囲であ
り、特に10 9 〜1014Ω・cmの範囲が好ましい。被
覆層の固有抵抗をこのような範囲とするには、樹脂10
0重量部及び70重量部を超え200重量部以下の10
0 〜105 Ω・cmの導電性粉体を含有する材料で被覆
層を形成することにより達成できる。導電性粉体の固有
抵抗は、好ましくは100 〜103 Ω・cmであり、樹
脂100重量部に対する導電性粉体の含有量は、好まし
くは80〜170重量部である。固有抵抗が105 Ω・
cmを超える導電性粉体を用いると、被覆層の固有抵抗
が高くなりすぎ、所望の固有抵抗を得るためには導電性
粉体量が過剰となるので、被覆層が脆くなり、使用時に
被覆層が割れることがある。また、100 Ω・cm未満
の導電性粉体を用いると、現像剤担持体を長期間使用し
た場合、被覆層が摩耗して導電性粉体が表面に露出し、
このため、被覆層の表面抵抗が著しく低下し、現像剤担
持体上の現像剤の帯電量が不足し、白地画像のかぶりや
黒画像の濃度低下ムラなどの画像不良の原因となり、本
発明の目標が達成されない。このような導電性粉体とし
て具体的には、硫酸バリウム表面に酸化スズ系導電層が
形成されたパストランTYPE−IV4410B[三井金
属鉱業株式会社製,2×10Ω・cm]やパストランT
YPE−IV4350[三井金属鉱業株式会社製,3×1
04 Ω・cm],酸化チタンの表面に酸化スズ系導電膜
が形成されたW−1−P[三菱マテリアル株式会社製,
101 Ω・cm],酸化スズ系のT−1[三菱マテリア
ル株式会社製,100 Ω・cm],導電性酸化亜鉛の2
3−K[白水化学工業株式会社製,2×102 Ω・c
m]等及びこれらの混合物などが挙げられる。なお、導
電性粉体の固有抵抗は、安藤電気株式会社製のAS−2
0646及びSE−43型粉体用電極を用い、10gの
粉体を電極間に入れ、100kg/cm2 で電極間を加
圧し、電気抵抗をテスターにて測定し、電極面積と、加
圧時の粉体の厚さを換算することにより求めた値であ
る。The coating layer according to the present invention comprises the above-mentioned crosslinkable resin or the like.
The main component is
Further improvement of power, reduction of frictional force with other members and conductivity
Charge control agent, lubricant, conductive agent, etc.
Various additives such as resin can be contained. Departure
In a light developer carrier, the resistance of such a coating layer
Is higher than the resistance of the conductive elastic layer.
It is preferable to adjust the resistance of the holding body, and this coating layer is preferable.
New specific resistance is 107-1016Ω · cm
Especially 10 9-1014The range of Ω · cm is preferable. Suffered
In order to set the specific resistance of the covering layer in such a range, the resin 10
0 parts by weight and more than 70 parts by weight and not more than 200 parts by weight
0-10FiveCoated with material containing conductive powder of Ωcm
This can be achieved by forming a layer. Inherent of conductive powder
The resistance is preferably 100-10ThreeΩ · cm, tree
The content of the conductive powder to 100 parts by weight of the fat is preferably
Or 80 to 170 parts by weight. Specific resistance is 10FiveΩ
cm or less, the resistivity of the coating layer
Is too high and conductive to achieve the desired resistivity
As the amount of powder becomes excessive, the coating layer becomes brittle and
The coating layer may crack. Also, 100Less than Ω · cm
The use of conductive powder makes it possible to use the developer
If the coating layer wears, the conductive powder is exposed on the surface,
As a result, the surface resistance of the coating layer is significantly reduced, and
Insufficient charge of the developer on the carrier, fog on white background
This may cause image defects such as uneven density reduction of black images,
The goal of the invention is not achieved. Such conductive powder
Specifically, a tin oxide conductive layer is formed on the surface of barium sulfate.
Formed Pastoran TYPE-IV4410B [Mitsui Kin
2 × 10Ω · cm] and Pastoran T
YPE-IV4350 [Mitsui Metal Mining Co., Ltd., 3 × 1
0FourΩ · cm], tin oxide conductive film on the surface of titanium oxide
Formed with W-1-P [Mitsubishi Materials Corporation,
101Ω · cm], tin oxide T-1 [Mitsubishi Materia
Le Co., Ltd., 100Ω · cm], 2 of conductive zinc oxide
3-K [2 × 10 by Hakusui Chemical Industry Co., Ltd.TwoΩ ・ c
m] and mixtures thereof. In addition,
The specific resistance of the conductive powder is AS-2 manufactured by Ando Electric Co., Ltd.
Using 0646 and SE-43 type powder electrodes
Put powder between electrodes, 100kg / cmTwoBetween the electrodes with
And measure the electrical resistance with a tester.
This is the value obtained by converting the thickness of the powder when pressed.
You.
【0015】現像剤担持体の抵抗としては106 〜10
12Ωが好ましく、107 〜1010Ωが特に好ましい。ま
た、被覆層を形成した現像剤担持体の表面粗さは、JI
S10点平均粗さで、10μmRz以下、特に0.3〜8
μmRzとすることが好ましい。この平均粗さが10μ
mRzを超えると、現像剤の帯電量が小さくなったり逆
帯電現像剤が生じて、画像かぶりを生じるので好ましく
ない。また、Rzが小さすぎると現像剤担持量が少なく
なり、画像濃度が低下する恐れが生じる。本発明の現像
剤担持体における被覆層の形成方法については特に制限
はないが、通常は、架橋性樹脂、架橋剤、及び必要に応
じて各種添加剤を溶解又は分散させてなる塗工液をディ
ッピング法,ロールコーター法,ドクターブレード法,
スプレー法などにより、導電性弾性層上に塗布した後、
常温あるいは50〜170℃程度の温度で乾燥し、架橋
硬化させて形成する。The resistance of the developer carrying member is 10 6 to 10
12 Ω is preferred, and 10 7 to 10 10 Ω is particularly preferred. Further, the surface roughness of the developer carrying member on which the coating layer is formed is determined by JI
S10 average roughness of 10 points or less, particularly 0.3 to 8
It is preferably set to μmRz. This average roughness is 10μ
If it exceeds mRz, the amount of charge of the developer becomes small or a reverse-charged developer is generated, which causes image fog, which is not preferable. On the other hand, if Rz is too small, the amount of developer carried is reduced, and the image density may be reduced. The method for forming the coating layer on the developer carrier of the present invention is not particularly limited, but usually, a coating solution obtained by dissolving or dispersing a crosslinkable resin, a crosslinker, and various additives as necessary. Dipping method, roll coater method, doctor blade method,
After applying it on the conductive elastic layer by spraying, etc.,
It is formed by drying at room temperature or at a temperature of about 50 to 170 ° C., and crosslinking and curing.
【0016】この被覆層の厚さは、1〜50μm程度と
することができるが、特に2〜30μmの範囲が好まし
い。この被覆層の厚さが薄すぎると局所的な放電が起こ
り、画像に白横線が発生しやすくなる。また、厚すぎる
と現像剤担持体が硬くなり、現像剤に損傷を与えて画像
形成体や成層ブレードへの現像剤固着などが発生して画
像不良の原因となる。上記塗工液の調製に用いられる溶
媒としては、例えばメタノール,エタノール,イソプロ
パノール,ブタノール等のアルコール系溶媒、アセト
ン,メチルエチルケトン,シクロヘキサノン等のケトン
系溶媒、トルエン,キシレン等の芳香族炭化水素系溶
媒、ヘキサン等の脂肪族炭化水素系溶媒、シクロヘキサ
ン等の脂環式炭化水素系溶媒、酢酸エチル等のエステル
系溶媒、イソプロピルエーテル,テトラヒドロフラン等
のエーテル系溶媒、ジメチルホルムアミド等のアミド系
溶媒、クロロホルム,シクロロエタン等のハロゲン化炭
化水素系溶媒等、及びこれらの混合溶媒などが挙げられ
る。本発明においては、ケトン系溶媒及びケトン系溶媒
と芳香族系炭化水素との混合溶媒が特に好ましく用いら
れる。The thickness of the coating layer can be about 1 to 50 μm, but is particularly preferably in the range of 2 to 30 μm. If the thickness of the coating layer is too small, local discharge occurs, and horizontal white lines are likely to occur in the image. On the other hand, if the thickness is too large, the developer carrying member becomes hard and damages the developer, causing the developer to adhere to the image forming body or the layered blade, thereby causing an image defect. Examples of the solvent used for preparing the coating liquid include alcohol solvents such as methanol, ethanol, isopropanol and butanol; ketone solvents such as acetone, methyl ethyl ketone and cyclohexanone; aromatic hydrocarbon solvents such as toluene and xylene; Aliphatic hydrocarbon solvents such as hexane; alicyclic hydrocarbon solvents such as cyclohexane; ester solvents such as ethyl acetate; ether solvents such as isopropyl ether and tetrahydrofuran; amide solvents such as dimethylformamide; Examples thereof include halogenated hydrocarbon solvents such as chloroethane and the like, and mixed solvents thereof. In the present invention, ketone solvents and mixed solvents of ketone solvents and aromatic hydrocarbons are particularly preferably used.
【0017】本発明の現像剤担持体は、電子写真装置に
おける現像装置などの画像形成装置に現像ローラ等とし
て組み込まれて用いられるものであり、例えば、図2に
示したように、トナーを供給するためのトナー塗布用ロ
ーラ5と静電潜像を保持した感光ドラム(画像形成体)
6との間に、本発明の現像剤担持体を現像ローラ1とし
て配置し、トナー塗布用ローラ5によりトナー7を担持
し、これを成層ブレード8により均一な薄層に整え、さ
らにこの薄層からトナーを感光ドラム(画像形成体)6
に供給し、感光ドラム(画像形成体)6の静電潜像にト
ナーを付着させて潜像を可視化するものである。図2に
示した画像形成装置の詳細については、上述の従来技術
において説明したので省略する。なお、本発明の現像剤
担持体を装着する画像形成装置は、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、この状態で画像形成体に接触又は近接して、該
画像形成体表面に現像剤を供給することにより、画像形
成体表面に可視画像を形成するものであればいずれのも
のでもよい。例えば、紙やOHP用紙等の紙葉類を画像
形成体とし、ごれらに現像剤担持体上に担持させた現像
剤を制御電極に形成した孔を通して直接飛翔せしめ、紙
やOHP用紙に直接画像を形成させるものであってもよ
い。The developer carrying member of the present invention is used by being incorporated as a developing roller or the like in an image forming apparatus such as a developing device in an electrophotographic apparatus. For example, as shown in FIG. Drum (image forming body) holding toner applying roller 5 and electrostatic latent image
6, the developer carrying member of the present invention is disposed as a developing roller 1, and a toner 7 is carried by a toner applying roller 5, which is formed into a uniform thin layer by a layering blade 8. From the photosensitive drum (image forming body) 6
And makes toner adhere to the electrostatic latent image on the photosensitive drum (image forming body) 6 to visualize the latent image. The details of the image forming apparatus shown in FIG. Note that the image forming apparatus to which the developer carrying member of the present invention is attached is not limited to the one shown in FIG. 2, and the developer is carried on the surface to form a thin layer of the developer. Any material may be used as long as it forms a visible image on the surface of the image forming body by supplying a developer to the surface of the image forming body in contact with or close to the forming body. For example, paper such as paper or OHP paper is used as an image forming body, and the developer carried on the developer carrier is directly scattered through the holes formed in the control electrodes, and directly onto the paper or OHP paper. It may be one that forms an image.
【0018】また、本発明の現像剤担持体に担持させる
現像剤としては、非磁性の一成分トナーが好適に用いら
れるが、磁性タイプの一成分現像剤を用いることもで
き、例えば磁性一成分トナーを用いて白黒画像印字を行
う場合にも、本発明の現像剤担持体及び画像形成装置を
好適に用いることができる。As the developer carried on the developer carrier of the present invention, a non-magnetic one-component toner is preferably used, but a magnetic one-component developer can also be used. Even when monochrome image printing is performed using toner, the developer carrier and the image forming apparatus of the present invention can be suitably used.
【0019】[0019]
【実施例】次に、本発明を実施例によりさらに具体的に
説明するが、本発明は、これらの例によってなんら限定
されるものではない。なお、実施例及び比較例で得られ
たトナー担持体について、下記の要領で特性試験を行っ
た。 (1)被覆層の層厚 被試験ローラの垂直切断面を走査型電子顕微鏡により観
察して測定した。 (2)被覆層の溶剤不溶率 被試験ローラとは別に、ガラス板を用意して、各ローラ
の被覆層形成に用いた塗工液をガラス板に塗布し、各ロ
ーラの作製と同一の条件で塗膜を加熱し、硬化させて塗
膜試料を作製した。このガラス板を、塗工液の調製に用
いたものと同様の溶媒中に常温で24時間浸漬した後、
乾燥させて、浸漬前後の塗膜の重量を測定し、下記の式
により溶剤不溶率を算出し、ローラの被覆層の溶剤不溶
率とし、この被覆層の溶剤不溶率が70重量%以上かど
うかを確認した。溶剤不溶率はいずれも90重量%以上
であった。 溶剤不溶率=〔(溶剤に浸漬、乾燥後の塗膜重量)/
(溶剤に浸漬前の塗膜重量)〕×100(重量%)EXAMPLES Next, the present invention will be described more specifically with reference to examples, but the present invention is not limited to these examples. In addition, the toner carrier obtained in each of Examples and Comparative Examples was subjected to a characteristic test in the following manner. (1) Layer Thickness of Coating Layer A vertical section of the roller to be tested was observed and measured with a scanning electron microscope. (2) Solvent insolubility of the coating layer A glass plate was prepared separately from the roller to be tested, and the coating liquid used for forming the coating layer of each roller was applied to the glass plate. The coating film was heated and cured to prepare a coating film sample. After immersing this glass plate in a solvent similar to that used for preparing the coating liquid at room temperature for 24 hours,
After drying, the weight of the coating film before and after immersion is measured, the solvent insolubility is calculated by the following equation, and the solvent insolubility of the coating layer of the roller is determined. Whether the solvent insolubility of the coating layer is 70% by weight or more It was confirmed. The solvent insolubility was 90% by weight or more in each case. Solvent insolubility = [(coating weight after immersion in solvent and drying) /
(Coating weight before immersion in solvent)] x 100 (% by weight)
【0020】(3)被覆層のガラス転移点の測定 JIS K7121のプラスチックの転移温度測定方法
に従って示差走査熱量(DSC)により測定し、得られ
たDSC曲線より中間点ガラス転移温度Tg(℃)を求
めた。 (4)被覆層の動的粘弾性の測定 動的弾性率E’〔Log(dyn/cm2 )〕及び損失
正接tanδは、動的粘弾性測定装置レオログラフSO
LID(東京精密社製)により測定した。測定条件は、
室温(約25℃)でSET STRAIN:0.5%、S
TATICSTRAIN:1.0%、周波数:5Hzとし
た。 (5)表面粗さ(Rz) 被試験ローラについて、表面粗さ計サーフコム590A
(東京精密社製)を用い、軸方向に対して直行した向き
(円周方向)に測定長さ2.4mm、測定速さ0.3mm/
sec、カットオフ波長0.8mmで、ローラのシャフト
方向及び円周方向で偏りがないように、300箇所以上
測定した値を平均してJIS10点平均粗さを求めた。 (6)被覆層の抵抗(膜抵抗) ローラとは別に、銅板を用意して、各ローラの被覆層形
成に用いた塗料膜を用いて、銅板上に該塗料液をバーコ
ータ塗布機で塗布し、各ローラと同条件で塗膜を加熱
し、硬化を行ない均一な薄膜を作成した。抵抗率計R8
340A(アドバンテスト社製)を用い、作製した薄膜
の厚さより電界強度5000V/cmになるように電圧
を印加して体積固有抵抗を求めた。 (7)ローラの抵抗 被試験ローラの両端に各500gの荷重をかけて銅板上
に押し付け、抵抗率計R8340A(アドバンテスト社
製)を用い、100Vの電圧を印加して抵抗値を測定し
た。 (8)長期間運転 各トナー担持体を現像ローラとして図2に示した現像ユ
ニットに装着し、現像バイアス−400V、ブレードバ
イアス−600Vとし、平均粒径7μmの非磁性一成分
負帯電トナーを用い、線速50mm/秒の周速で回転さ
せながら反転現像で画像出しを行った。初期には各トナ
ー担持体で白地画像及び黒字画像において良好な画像が
出ることを確認した。長期間運転条件として5%印字パ
ターンにおいてA4サイズ用紙を横方向に1万枚の印刷
を行った。 (9)トナー帯電量 上記の同装置条件にて長期間運転を行った後に、現像ロ
ーラ表面に形成された均一なトナー薄層を吸引してファ
ラディゲージ内に導入し、電荷量を測定した。これと同
時に吸引されたトナー重量も測定し、単位重量当たりの
トナー帯電量(μC/g)を求めた。 (10)画像評価 長期間運転を行った後に、白地画像及び黒地画像におけ
る画像評価を行った。白地画像において画像のかぶりが
多く生じた場合を×、画像のかぶりが発生せず良好であ
った場合を○で示した。黒地画像では、濃度低下ムラに
ついて、黒濃度ムラが発生した場合を×、黒濃度ムラが
発生せず良好であった場合を○で示した。また、マクベ
ス濃度計RD918(Kollmorgen Instruments Corpora
tion製)を用いて黒濃度を測定し数値化した。(3) Measurement of Glass Transition Temperature of Coating Layer The glass transition temperature Tg (° C.) of the intermediate point was measured by differential scanning calorimetry (DSC) in accordance with the method for measuring the transition temperature of plastic according to JIS K7121. I asked. (4) Measurement of Dynamic Viscoelasticity of Coating Layer The dynamic elastic modulus E ′ [Log (dyn / cm 2 )] and the loss tangent tan δ were measured by a dynamic viscoelasticity measuring apparatus rheograph SO.
It was measured by LID (Tokyo Seimitsu Co., Ltd.). The measurement conditions are
At room temperature (about 25 ° C) SET STRAIN: 0.5%, S
TATICSTRAIN: 1.0%, frequency: 5 Hz. (5) Surface roughness (Rz) For the roller to be tested, use a surface roughness meter Surfcom 590A.
(Manufactured by Tokyo Seimitsu Co., Ltd.) in a direction perpendicular to the axial direction (circumferential direction), measuring length 2.4 mm, measuring speed 0.3 mm /
The values measured at 300 points or more were averaged to obtain the JIS 10-point average roughness so that the cut-off wavelength was 0.8 mm and there was no deviation in the shaft direction and circumferential direction of the roller. (6) Resistance of coating layer (film resistance) A copper plate is prepared separately from the roller, and the coating liquid is applied to the copper plate by a bar coater using a coating film used for forming the coating layer of each roller. Then, the coating film was heated under the same conditions as those of each roller, and cured to form a uniform thin film. Resistivity meter R8
Using 340A (manufactured by Advantest), a voltage was applied so that the electric field strength became 5000 V / cm from the thickness of the formed thin film, and the volume resistivity was obtained. (7) Resistance of Roller A load of 500 g was applied to both ends of the roller to be tested, pressed against a copper plate, and a resistance value was measured by applying a voltage of 100 V using a resistivity meter R8340A (manufactured by Advantest). (8) Long-term operation Each toner carrier is attached to the developing unit shown in FIG. 2 as a developing roller, a developing bias is -400 V, a blade bias is -600 V, and a non-magnetic one-component negatively charged toner having an average particle diameter of 7 μm is used. An image was formed by reversal development while rotating at a linear speed of 50 mm / sec. Initially, it was confirmed that a good image appeared in a white background image and a black image on each toner carrier. As long-term operation conditions, 10,000 sheets of A4 size paper were printed in the horizontal direction in a 5% print pattern. (9) Toner Charge Amount After a long-term operation under the same apparatus conditions as described above, a uniform thin layer of toner formed on the surface of the developing roller was sucked and introduced into a Faraday gauge to measure the charge amount. At the same time, the weight of the sucked toner was also measured, and the toner charge per unit weight (μC / g) was determined. (10) Image evaluation After long-term operation, image evaluation was performed on a white background image and a black background image. The symbol x indicates that a large amount of image fog occurred in the white background image, and the symbol o indicates that the image was satisfactory without image fog. In the black background image, regarding the density reduction unevenness, the case where black density unevenness occurred was indicated by x, and the case where black density unevenness did not occur and was good was indicated by ○. In addition, Macbeth densitometer RD918 (Kollmorgen Instruments Corpora)
The density of the black was measured using the method described in the above section and was quantified.
【0021】実施例1 グリセリンにプロピレンオキサイドとエチレンオキサイ
ドを付加し、分子量5000としたポリエーテルポリオ
ール(OH価:33mgKOH/g)100部(重量
部、以下同じ)に1,4−ブタンジオール1.0部、ニッ
ケルアセチルアセトナト0.5部、ジブチルチンジラウレ
ート0.01部及びアセチレンブラック2.0部を添加し、
混合機を用いて混合してポリオール組成物を調製した。
このポリオール組成物を減圧下に攪拌して脱泡した後、
ウレタン変性MDI(ジフェニルメタンジイソシアネー
ト)を17.5部加えて2分間攪拌し、これを、ニッケル
メッキ鋼製のシャフトを配置し予め110℃に加熱した
金型に注型し、110℃で2時間硬化させてシャフトの
外周に導電性弾性層を形成してローラを得た。得られた
ローラの表面を研磨して、表面をJIS10点平均粗さ
10.5μmRz に調整した。なお、この表面粗さは、上
述したように、表面粗さ計「サーフコム590A」(東
京精密社製)を用いて測定した(以下の例においても同
様)。バインダー樹脂としてアルコキシシリル基含有ア
クリル共重合体であるゼムラックYC3372(鐘淵化
学工業株式会社製,固形分率50重量%)、脱水剤とし
て有機エステル類のZW806Z(鐘淵化学工業株式会
社製)、硬化触媒として有機スズ系のゼムラックBT1
20S(鐘淵化学工業株式会社製)、導電性粉体として
硫酸バリウム表面に酸化スズ系導電層が形成されたパス
トランTYPE−IV4410B(三井金属鉱業株式会社
製)を用い、溶媒としてMEK(メチルエチルケトン)
を用い、第1表に示す組成(第1表において配合量は重
量部で示す、以下同じ)の塗工液を調製した。当該塗工
液中に、上記ローラを浸漬して引き上げ、これを110
℃にて4時間加熱し、架橋硬化した被覆層を有する図1
と同様のローラ状トナー担持体を得た。Example 1 Propylene oxide and ethylene oxide were added to glycerin to give 100 parts (parts by weight, hereinafter the same) of a polyether polyol (OH value: 33 mgKOH / g) having a molecular weight of 5,000. 0 parts, nickel acetylacetonate 0.5 parts, dibutyltin dilaurate 0.01 parts and acetylene black 2.0 parts,
The mixture was mixed using a mixer to prepare a polyol composition.
After degassing by stirring this polyol composition under reduced pressure,
17.5 parts of urethane-modified MDI (diphenylmethane diisocyanate) was added, and the mixture was stirred for 2 minutes. The mixture was poured into a mold having a nickel-plated steel shaft placed therein and heated to 110 ° C. in advance, and cured at 110 ° C. for 2 hours. Then, a conductive elastic layer was formed on the outer periphery of the shaft to obtain a roller. The surface of the obtained roller was polished, and the surface was adjusted to a JIS 10-point average roughness of 10.5 μmRz. As described above, the surface roughness was measured using a surface roughness meter “Surfcom 590A” (manufactured by Tokyo Seimitsu Co., Ltd.) (the same applies to the following examples). Zemlac YC3372, an alkoxysilyl group-containing acrylic copolymer (manufactured by Kanegafuchi Chemical Co., Ltd., solid content: 50% by weight) as a binder resin, ZW806Z of organic esters as a dehydrating agent (Kanebuchi Chemical Industry Co., Ltd.), Organotin Zemrak BT1 as curing catalyst
20S (manufactured by Kanegafuchi Chemical Industry Co., Ltd.), Pastran TYPE-IV4410B (manufactured by Mitsui Mining & Smelting Co., Ltd.) having a tin oxide-based conductive layer formed on the surface of barium sulfate as a conductive powder, and MEK (methyl ethyl ketone) as a solvent.
Was used to prepare a coating liquid having the composition shown in Table 1 (the blending amount in Table 1 is shown in parts by weight, the same applies hereinafter). The roller is immersed in the coating liquid and pulled up.
FIG. 1 having a coating layer cured by crosslinking at 4 ° C. for 4 hours
The same roller-shaped toner carrier as in Example 1 was obtained.
【0022】実施例2 バインダー樹脂として、アルコキシシリル基含有アクリ
ル共重合体であるゼムラックYC3372(鐘淵化学工
業株式会社製、固形分率50重量%)及びメラミン樹脂
であるスーパーペッカミンL117(大日本インキ化学
工業株式会社製、固形分率60重量%)を用いて第1表
に示す組成の塗工液を調製し、この塗工液を用いて被覆
層を形成した以外は実施例1と同様にしてローラ状トナ
ー担持体を作製した。 実施例3 実施例2において、導電性粉体パストランTYPE−IV
4410B(三井金属鉱業株式会社製)を減量し、第1
表に示す組成の塗工液を調製し、この塗工液を用いて被
覆層を形成した以外は実施例1と同様にしてローラ状ト
ナー担持体を作製した。 実施例4 実施例3において、導電性粉体をパストランTYPE−
IV4410Bに比べて抵抗が高いIV4350(三井金属
鉱業株式会社製)に代え、第1表に示す組成の塗工液を
調製し、この塗工液を用いて被覆層を形成した以外は実
施例1と同様にしてローラ状トナー担持体を作製した。Example 2 As a binder resin, Zemlac YC3372 (alkane silyl group-containing acrylic copolymer, manufactured by Kanegafuchi Chemical Co., Ltd., solid content: 50% by weight) and melamine resin Superpecamine L117 (Dainippon) Ink Chemical Industry Co., Ltd., solid content ratio 60% by weight) was used to prepare a coating liquid having the composition shown in Table 1, and the coating liquid was used to form a coating layer. Thus, a roller-shaped toner carrier was produced. Example 3 In Example 2, the conductive powder pastelan TYPE-IV was used.
4410B (Mitsui Metal Mining Co., Ltd.)
A coating liquid having the composition shown in the table was prepared, and a roller-shaped toner carrier was produced in the same manner as in Example 1 except that a coating layer was formed using this coating liquid. Example 4 In Example 3, the conductive powder was replaced with Pastoran TYPE-
Example 1 was repeated except that a coating solution having the composition shown in Table 1 was prepared in place of IV4350 (manufactured by Mitsui Mining & Smelting Co., Ltd.), which had higher resistance than IV4410B, and a coating layer was formed using this coating solution. In the same manner as in the above, a roller-shaped toner carrier was produced.
【0023】実施例5 バインダー樹脂として、官能基を有するポリスチレンブ
タジエン樹脂であるタフテックM1962(旭化成工業
株式会社製)及びメラミン樹脂であるスーパーベッカミ
ンL145(大日本インキ化学工業株式会社製,固形分
率60重量%)を用い、導電性粉体としてパストランT
YPE−IV4410B(三井金属鉱業株式会社製)を用
い、硬化促進剤として燐酸エステルであるP198(大
日本インキ化学工業株式会社製)を、分散剤としてスル
パースS3000(ゼネカ株式会社製)を添加し、溶媒
としてトルエンを用い、第1表に示す組成の塗工液を調
製し、この塗工液を用いて被覆層を形成した以外は実施
例1と同様にしてローラ状トナー担持体を作製した。Example 5 As binder resins, Tuftec M1962, a polystyrene butadiene resin having a functional group (manufactured by Asahi Kasei Kogyo Co., Ltd.), and Super Beckamine L145, a melamine resin (manufactured by Dainippon Ink and Chemicals, Inc., solid content ratio) 60% by weight) and pastelan T as a conductive powder.
Using YPE-IV4410B (manufactured by Mitsui Mining & Smelting Co., Ltd.), P198 (manufactured by Dainippon Ink and Chemicals, Inc.) as a curing accelerator and Sulpers S3000 (manufactured by Zeneca Corporation) as a dispersant were added. A coating liquid having the composition shown in Table 1 was prepared using toluene as a solvent, and a roller-shaped toner carrier was produced in the same manner as in Example 1 except that a coating layer was formed using this coating liquid.
【0024】実施例6 実施例5において、タフテックM1962に代えて熱可
塑性の飽和共重合ポリエステル樹脂であるエリーテルU
E3400(ユニチカ株式会社製)を用い、分散剤とし
てソルパースS24000(ゼネカ株式会社製)を用
い、溶媒としてMEKを用い、第1表に示す組成の塗工
液を調製し、この塗工液を用いて被覆層を形成した以外
は実施例1と同様にしてローラ状トナー担持体を作製し
た。 実施例7 実施例6において、エリーテルUE3400に代えて熱
可塑性のアクリル樹脂であるダイヤナールLR−258
2(三菱レイヨン株式会社製、固形分率60重量%)を
用い、溶媒としてトルエンとエタノールの混合溶媒を用
い、第1表に示す組成の塗工液を調製し、この塗工液を
用いて被覆層を形成した以外は実施例1と同様にしてロ
ーラ状トナー担持体を作製した。Example 6 In Example 5, a thermoplastic saturated copolyester resin, Elitel U, was used in place of Tuftec M1962.
Using E3400 (manufactured by Unitika Corporation), Solpers S24000 (manufactured by Zeneca Corporation) as a dispersant, MEK as a solvent, and preparing a coating solution having the composition shown in Table 1, and using this coating solution. A roller-shaped toner carrier was produced in the same manner as in Example 1 except that the coating layer was formed by the above method. Example 7 In Example 6, Dynal LR-258 which is a thermoplastic acrylic resin in place of Elitel UE3400 is used.
2 (manufactured by Mitsubishi Rayon Co., Ltd., solid content: 60% by weight), a mixed solvent of toluene and ethanol was used as a solvent to prepare a coating liquid having the composition shown in Table 1, and this coating liquid was used. A roller-shaped toner carrier was produced in the same manner as in Example 1 except that the coating layer was formed.
【0025】比較例1 実施例1において、導電性粉体パストランTYPE−IV
4410Bに代えて、予め溶剤に分散させたカーボンブ
ラック#220(御国色素株式会社製,固形分率40重
量%)を用い、溶媒としてトルエンを用いて第1表に示
す組成の塗工液を調製し、この塗工液を用いて被覆層を
形成した以外は実施例1と同様にしてローラ状トナー担
持体を作製した。 比較例2 実施例2において、導電性粉体パストランTYPE−IV
4410Bに代えて、予め溶剤に分散させたカーボンブ
ラック#220(御国色素株式会社製,固形分率40重
量%)を用い、溶媒としてトルエンを用いて第1表に示
す組成の塗工液を調製し、この塗工液を用いて被覆層を
形成した以外は実施例1と同様にしてローラ状トナー担
持体を作製した。Comparative Example 1 In Example 1, the conductive powder Pastrun TYPE-IV was used.
Instead of 4410B, a coating liquid having the composition shown in Table 1 was prepared using carbon black # 220 (manufactured by Mikuni Dye Co., Ltd., solid content: 40% by weight) previously dispersed in a solvent and using toluene as a solvent. Then, a roller-shaped toner carrier was produced in the same manner as in Example 1 except that a coating layer was formed using this coating liquid. Comparative Example 2 In Example 2, conductive powder pastelan TYPE-IV
Instead of 4410B, a coating liquid having the composition shown in Table 1 was prepared using carbon black # 220 (manufactured by Mikuni Dye Co., Ltd., solid content: 40% by weight) previously dispersed in a solvent and using toluene as a solvent. Then, a roller-shaped toner carrier was produced in the same manner as in Example 1 except that a coating layer was formed using this coating liquid.
【0026】[0026]
【表1】 [Table 1]
【0027】[0027]
【表2】 [Table 2]
【0028】第1表に示す結果から、実施例のトナー担
持体は、長期間使用しても著しいローラ抵抗の変化もな
く、良好なトナー帯電性を示し、白地画像のかぶり、黒
画像の濃度低下ムラも発生せず、良好な画像が安定的に
得られるものであることが確認できた。From the results shown in Table 1, it can be seen that the toner carriers of the examples show good toner chargeability without significant change in roller resistance even after long-term use, fog of white background images, and density of black images. It was confirmed that no deterioration unevenness was generated and a good image was stably obtained.
【0029】[0029]
【発明の効果】本発明の現像剤担持体は、長期間使用し
ても良好な現像剤帯電性を示し、白地画像のかぶり、黒
画像の濃度低下ムラも発生せず、良好な画像が安定的に
得られるものでありて、各種画像形成装置の現像剤担持
体として好適に用いられる。According to the present invention, the developer carrier of the present invention exhibits good developer chargeability even when used for a long period of time. And is suitably used as a developer carrier of various image forming apparatuses.
【図1】 本発明の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 sectional view showing an example of a developer carrying member of the present invention.
【図2】 本発明の画像形成装置の一例を示す概略断面
図である。FIG. 2 is a schematic sectional view showing an example of the image forming apparatus of the present invention.
1:トナー担持体(現像ローラ) 2:シャフト 3:導電性弾性層 4:被覆層 5:トナー塗布用ローラ 6:画像形成体(感光体) 7:トナー 8:成層ブレード 9:転写部 10:クリーニング部 11:クリーニングブレード 1: toner carrier (developing roller) 2: shaft 3: conductive elastic layer 4: coating layer 5: toner applying roller 6: image forming body (photoreceptor) 7: toner 8: layered blade 9: transfer unit 10: Cleaning section 11: Cleaning blade
フロントページの続き Fターム(参考) 2H077 AD06 EA13 EA14 EA15 EA16 FA01 FA13 FA22 FA25 3J103 AA02 AA14 AA23 AA51 BA41 FA12 FA30 GA02 GA52 GA57 GA58 GA60 HA03 HA12 HA20 HA41 HA45 HA47 HA53 4J002 AA011 AC011 AC031 AC061 AC071 AC081 AC091 BB151 BB171 BC051 BG031 CC181 CF001 CH041 CK021 CP031 DA026 DA036 DE096 DE106 DE136 DE186 DE196 DK006 EN136 EV186 EV256 FA086 FD116 Continued on front page F term (reference) 2H077 AD06 EA13 EA14 EA15 EA16 FA01 FA13 FA22 FA25 3J103 AA02 AA14 AA23 AA51 BA41 FA12 FA30 GA02 GA52 GA57 GA58 GA60 HA03 HA12 HA20 HA41 HA45 HA47 HA53 4J002 AA011 AC011 AC031 AC06 BC1 BG031 CC181 CF001 CH041 CK021 CP031 DA026 DA036 DE096 DE106 DE136 DE186 DE196 DK006 EN136 EV186 EV256 FA086 FD116
Claims (12)
し、この状態で画像形成体に接触又は近接して、該画像
形成体表面に該現像剤を供給することにより、画像形成
体表面に可視画像を形成させる現像剤担持体において、
現像剤担持体が、導電性弾性層の表面に、樹脂100重
量部及び70重量部を超え200重量部以下の100 〜
105 Ω・cmの導電性粉体を含有する材料からなる被
覆層を有するものであることを特徴とする現像剤担持
体。An image forming member is formed by carrying a developer on the surface to form a thin film thereof, and in this state, contacting or approaching the image forming member and supplying the developer to the surface of the image forming member. In a developer carrier that forms a visible image on the surface,
Developer carrying member, the surface of the conductive elastic layer, the resin 100 parts by weight and 70 parts by weight of more than 200 parts by weight or less of 10 0 -
A developer carrier having a coating layer made of a material containing a conductive powder of 10 5 Ω · cm.
80°の硬度を有するものである請求項1記載の現像剤
担持体。2. The method according to claim 1, wherein the conductive elastic layer is of Asker C type having a thickness of 40 to 40.
The developer carrier according to claim 1, wherein the developer carrier has a hardness of 80 °.
レンプロピレンゴム及びウレタンゴムの中から選ばれる
少なくとも一種のゴム弾性体からなる請求項1又は2記
載の現像剤担持体。3. The developer carrier according to claim 1, wherein the conductive elastic layer is made of at least one rubber elastic material selected from butadiene rubber, ethylene propylene rubber, and urethane rubber.
010Ω・cm及び表面粗さがJIS10点平均粗さで1
5μmRz以下である請求項1〜3のいずれかに記載の
現像剤担持体。4. The conductive elastic layer has a specific resistance of 10 3 to 1
0 10 Ω · cm and surface roughness of JIS 10 point average roughness of 1
The developer carrier according to claim 1, wherein the developer carrier is 5 μmRz or less.
脂,スチレンブタジエン樹脂,ポリエステル樹脂,アク
リル変性シリコーン樹脂及びメラミン樹脂から選ばれる
少なくとも一種である請求項1〜4のいずれかに記載の
現像剤担持体。5. The developer according to claim 1, wherein the resin constituting the coating layer is at least one selected from an acrylic resin, a styrene-butadiene resin, a polyester resin, an acryl-modified silicone resin, and a melamine resin. Carrier.
ガラス転移点を持つものである請求項1〜5のいずれか
に記載の現像剤担持体。6. The developer carrier according to claim 1, wherein the resin constituting the coating layer has a glass transition point of 10 ° C. or less.
09.8 dyn/cm 2 であり、損失正接tanδが0.7
以下のものである請求項1〜6のいずれかに記載現像剤
担持体。7. The coating layer having a dynamic elastic modulus E ′ of 107~ 1
09.8dyn / cm TwoAnd the loss tangent tan δ is 0.7
The developer according to any one of claims 1 to 6, which is:
Carrier.
る請求項1〜7のいずれかに記載の現像剤担持体。8. The developer carrier according to claim 1, wherein the coating layer has a thickness of 1 to 50 μm.
量%以上のものである請求項1〜8のいずれかに記載の
現像剤担持体。9. The developer carrier according to claim 1, wherein the coating layer has an insolubility in a solvent of 70% by weight or more.
Ω・cmのものである請求項1〜9のいずれかに記載の
現像剤担持体。10. The coating layer has a specific resistance of 10 7 to 10 16.
The developer carrier according to any one of claims 1 to 9, wherein the developer carrier is Ω · cm.
Ω及び表面粗さがJIS10点平均粗さで10μmRz
以下である請求項1〜10のいずれかに記載の現像剤担
持体。11. The developer carrying member has a resistance of 10 3 to 10 12.
Ω and surface roughness are 10 μm Rz in JIS 10 point average roughness
The developer carrier according to claim 1, wherein:
現像剤担持体の表面に現像剤を担持してその薄膜を形成
し、この現像剤担持体を画像形成体に接触又は近接させ
て、該画像形成体表面に現像剤を供給することにより、
画像形成体表面に可視画像を形成させる画像形成装置に
おいて、上記現像剤担持体として、請求項1〜11のい
ずれかに記載の現像剤担持体を用いたことを特徴とする
画像形成装置。12. A developer carrier is mounted, and a developer is carried on the surface of the developer carrier to form a thin film, and the developer carrier is brought into contact with or close to the image forming body. By supplying a developer to the surface of the image forming body,
An image forming apparatus for forming a visible image on the surface of an image forming body, wherein the developer holding body according to claim 1 is used as the developer holding body.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20568399A JP4233691B2 (en) | 1999-07-21 | 1999-07-21 | Developer carrying member and image forming apparatus |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20568399A JP4233691B2 (en) | 1999-07-21 | 1999-07-21 | Developer carrying member and image forming apparatus |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2001034062A true JP2001034062A (en) | 2001-02-09 |
| JP4233691B2 JP4233691B2 (en) | 2009-03-04 |
Family
ID=16510979
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20568399A Expired - Fee Related JP4233691B2 (en) | 1999-07-21 | 1999-07-21 | Developer carrying member and image forming apparatus |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4233691B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006267244A (en) * | 2005-03-22 | 2006-10-05 | Tokai Rubber Ind Ltd | Semiconductive composition for electrophotographic equipment and semiconductive member for electrophotographic equipment obtained by using the same |
-
1999
- 1999-07-21 JP JP20568399A patent/JP4233691B2/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006267244A (en) * | 2005-03-22 | 2006-10-05 | Tokai Rubber Ind Ltd | Semiconductive composition for electrophotographic equipment and semiconductive member for electrophotographic equipment obtained by using the same |
Also Published As
| Publication number | Publication date |
|---|---|
| JP4233691B2 (en) | 2009-03-04 |
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