JPH01191883A - Electrophotographic process - Google Patents
Electrophotographic processInfo
- Publication number
- JPH01191883A JPH01191883A JP1830988A JP1830988A JPH01191883A JP H01191883 A JPH01191883 A JP H01191883A JP 1830988 A JP1830988 A JP 1830988A JP 1830988 A JP1830988 A JP 1830988A JP H01191883 A JPH01191883 A JP H01191883A
- Authority
- JP
- Japan
- Prior art keywords
- photoreceptor
- layer
- resin
- charge
- image
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 23
- 230000008569 process Effects 0.000 title claims description 13
- 239000000463 material Substances 0.000 claims abstract description 14
- 239000010410 layer Substances 0.000 claims description 86
- 108091008695 photoreceptors Proteins 0.000 claims description 68
- 239000011241 protective layer Substances 0.000 claims description 12
- 230000006866 deterioration Effects 0.000 abstract description 7
- 238000009833 condensation Methods 0.000 abstract description 5
- 230000005494 condensation Effects 0.000 abstract description 5
- 230000002411 adverse Effects 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 36
- 239000011347 resin Substances 0.000 description 36
- 238000000576 coating method Methods 0.000 description 31
- 239000011248 coating agent Substances 0.000 description 30
- 239000000126 substance Substances 0.000 description 23
- 239000007788 liquid Substances 0.000 description 18
- 239000000049 pigment Substances 0.000 description 17
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 14
- 239000011230 binding agent Substances 0.000 description 13
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 12
- 238000010438 heat treatment Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- -1 chromium Chemical compound 0.000 description 9
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 8
- 229910052782 aluminium Inorganic materials 0.000 description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 7
- 230000007423 decrease Effects 0.000 description 7
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 238000007664 blowing Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 4
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 4
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 229910010272 inorganic material Inorganic materials 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229920006122 polyamide resin Polymers 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 229920002050 silicone resin Polymers 0.000 description 3
- 239000002356 single layer Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 238000004544 sputter deposition Methods 0.000 description 3
- 238000010186 staining Methods 0.000 description 3
- 238000007740 vapor deposition Methods 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000005525 hole transport Effects 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- 230000031700 light absorption Effects 0.000 description 2
- SXQCTESRRZBPHJ-UHFFFAOYSA-M lissamine rhodamine Chemical compound [Na+].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=C(S([O-])(=O)=O)C=C1S([O-])(=O)=O SXQCTESRRZBPHJ-UHFFFAOYSA-M 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000005033 polyvinylidene chloride Substances 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 229910001887 tin oxide Inorganic materials 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- NGQSLSMAEVWNPU-YTEMWHBBSA-N 1,2-bis[(e)-2-phenylethenyl]benzene Chemical group C=1C=CC=CC=1/C=C/C1=CC=CC=C1\C=C\C1=CC=CC=C1 NGQSLSMAEVWNPU-YTEMWHBBSA-N 0.000 description 1
- VERMWGQSKPXSPZ-BUHFOSPRSA-N 1-[(e)-2-phenylethenyl]anthracene Chemical compound C=1C=CC2=CC3=CC=CC=C3C=C2C=1\C=C\C1=CC=CC=C1 VERMWGQSKPXSPZ-BUHFOSPRSA-N 0.000 description 1
- JOERSAVCLPYNIZ-UHFFFAOYSA-N 2,4,5,7-tetranitrofluoren-9-one Chemical compound O=C1C2=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C2C2=C1C=C([N+](=O)[O-])C=C2[N+]([O-])=O JOERSAVCLPYNIZ-UHFFFAOYSA-N 0.000 description 1
- VHQGURIJMFPBKS-UHFFFAOYSA-N 2,4,7-trinitrofluoren-9-one Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=C2C3=CC=C([N+](=O)[O-])C=C3C(=O)C2=C1 VHQGURIJMFPBKS-UHFFFAOYSA-N 0.000 description 1
- HJCNIHXYINVVFF-UHFFFAOYSA-N 2,6,8-trinitroindeno[1,2-b]thiophen-4-one Chemical compound O=C1C2=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C2C2=C1C=C([N+](=O)[O-])S2 HJCNIHXYINVVFF-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- JNGDCMHTNXRQQD-UHFFFAOYSA-N 3,6-dioxocyclohexa-1,4-diene-1,2,4,5-tetracarbonitrile Chemical compound O=C1C(C#N)=C(C#N)C(=O)C(C#N)=C1C#N JNGDCMHTNXRQQD-UHFFFAOYSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- MKYQPGPNVYRMHI-UHFFFAOYSA-N Triphenylethylene Chemical class C=1C=CC=CC=1C=C(C=1C=CC=CC=1)C1=CC=CC=C1 MKYQPGPNVYRMHI-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 238000002679 ablation Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 238000002048 anodisation reaction Methods 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical class C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-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
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- MRQIXHXHHPWVIL-UHFFFAOYSA-N chembl1397023 Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC1=CC=CC=C1 MRQIXHXHHPWVIL-UHFFFAOYSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- IYYZUPMFVPLQIF-ALWQSETLSA-N dibenzothiophene Chemical group C1=CC=CC=2[34S]C3=C(C=21)C=CC=C3 IYYZUPMFVPLQIF-ALWQSETLSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- YLQWCDOCJODRMT-UHFFFAOYSA-N fluoren-9-one Chemical group C1=CC=C2C(=O)C3=CC=CC=C3C2=C1 YLQWCDOCJODRMT-UHFFFAOYSA-N 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 229930195712 glutamate Natural products 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000000113 methacrylic resin Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- GACNTLAEHODJKY-UHFFFAOYSA-N n,n-dibenzyl-4-[1-[4-(dibenzylamino)phenyl]propyl]aniline Chemical compound C=1C=C(N(CC=2C=CC=CC=2)CC=2C=CC=CC=2)C=CC=1C(CC)C(C=C1)=CC=C1N(CC=1C=CC=CC=1)CC1=CC=CC=C1 GACNTLAEHODJKY-UHFFFAOYSA-N 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- 229910001120 nichrome Inorganic materials 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical group C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 150000007978 oxazole derivatives Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229910003446 platinum oxide Inorganic materials 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920001470 polyketone Polymers 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 239000011116 polymethylpentene Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
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- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920006215 polyvinyl ketone Polymers 0.000 description 1
- 229920002102 polyvinyl toluene Polymers 0.000 description 1
- 150000004032 porphyrins Chemical group 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- RCYFOPUXRMOLQM-UHFFFAOYSA-N pyrene-1-carbaldehyde Chemical compound C1=C2C(C=O)=CC=C(C=C3)C2=C2C3=CC=CC2=C1 RCYFOPUXRMOLQM-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
- NLDYACGHTUPAQU-UHFFFAOYSA-N tetracyanoethylene Chemical group N#CC(C#N)=C(C#N)C#N NLDYACGHTUPAQU-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
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- 125000006617 triphenylamine group Chemical group 0.000 description 1
- 229920006163 vinyl copolymer Polymers 0.000 description 1
Landscapes
- Discharging, Photosensitive Material Shape In Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
〔技術分野〕
本発明は電子写真感光体に関し、更に詳しくは電子写真
プロセスの改良に関する。DETAILED DESCRIPTION OF THE INVENTION [Technical Field] The present invention relates to an electrophotographic photoreceptor, and more particularly to improvements in electrophotographic processes.
電子写真複写機に使用される感光体は、近年、安価、生
産性、無公害性を利点とする有機系の感光材料を用いた
ものが使用され始めている。In recent years, photoreceptors used in electrophotographic copying machines have begun to be made of organic photosensitive materials, which have the advantages of low cost, productivity, and non-polluting properties.
有機系の電子写真感光体には、ポリビニルカルバゾール
(PVK)に代表される光導電性樹脂、PVK−TNF
(2,4,7トリニトロフルオレノン)に代表される電
荷移動錯体型、フタロシアニン−バインダーに代表され
る顔料分散型、電荷発生物質と電荷輸送物質とを組合せ
て用いる機能分離型の感光体などが知られており、特に
機能分離型の感光体が注目されている。Organic electrophotographic photoreceptors include photoconductive resins such as polyvinylcarbazole (PVK), and PVK-TNF.
There are charge transfer complex type photoreceptors represented by (2,4,7 trinitrofluorenone), pigment dispersion types represented by phthalocyanine binders, and functionally separated type photoreceptors that use a combination of a charge generating substance and a charge transporting substance. In particular, functionally separated type photoreceptors are attracting attention.
この様な、有機系感光体を、カールソンプロセスに適用
した場合、帯電性が低く、電荷保持性が悪い(暗減衰が
大きい)上、繰返し使用による、これら特性の劣化が大
きく、画像上に、濃度ムラ、カブリ、また反転現像の場
合地汚れを生ずるといいう欠点を有している。When such an organic photoreceptor is applied to the Carlson process, it has low chargeability and poor charge retention (high dark decay), and these characteristics deteriorate significantly with repeated use, causing problems such as It has the drawbacks of density unevenness, fog, and background smearing in the case of reverse development.
即ち、有機系感光体は、前露光疲労によって帯電性が低
下する。この前露光疲労は主に電荷発生材料が吸収する
光によって起こることから、光吸収によって発生した電
荷が移動可能な状態で感光体内に残留している時間が長
い程、またその電荷の数が多い程、前露光疲労による帯
電性の低下が著しくなると考えられる。即ち、光吸収に
よって発生した電荷が残留している状態で帯電操作をし
ても、残留しているキャリアの移動で表面電荷が中和さ
れる為、残留電荷が消費されるまで表面電位は上昇しな
い。従って、前露光疲労分だけ表面電位の上昇が遅れる
ことになり、見かけ上の帯電4位は低くなる。That is, the chargeability of organic photoreceptors decreases due to pre-exposure fatigue. This pre-exposure fatigue is mainly caused by light absorbed by the charge-generating material, so the longer the charges generated by light absorption remain in the photoconductor in a mobile state, the more the number of charges increases. It is thought that the lower the chargeability becomes, the more the chargeability decreases due to pre-exposure fatigue. In other words, even if a charging operation is performed while the charge generated by light absorption remains, the surface charge will be neutralized by the movement of the remaining carriers, so the surface potential will increase until the residual charge is consumed. do not. Therefore, the increase in surface potential is delayed by the amount of pre-exposure fatigue, and the apparent charge level 4 becomes lower.
これらの欠点を改良する方法として、支持体と電荷発生
層との間にSiOSlolA、等の無機材料を。As a method to improve these drawbacks, an inorganic material such as SiOSlolA is used between the support and the charge generation layer.
蒸着、スパッタリング、陽極酸化などの方法で設ける方
法が公知であり、電荷発生層中にUi、 o、を含有さ
せたり(特開昭55−142354号公報)、同じく電
荷発生層中に金属粉末を含有させることも公知である(
特開昭60−214364号公報)。Methods such as vapor deposition, sputtering, and anodic oxidation are known, and Ui, O, etc. are included in the charge generation layer (Japanese Unexamined Patent Publication No. 55-142354), and metal powder is also included in the charge generation layer. It is also known to contain (
(Japanese Patent Application Laid-Open No. 60-214364).
また、下引層としてポリアミド樹脂(特開昭58−30
757号公報、特開昭58−98739号公報)、アル
コール可溶性ナイロン樹脂(特開昭60−196766
号公報)、水溶性ポリビニルブチラール樹脂(特開昭6
0−232553号公報)、ポリビニルブチラール樹脂
(特開昭58−106549号公報)などの樹脂層が提
案されている。In addition, polyamide resin (Japanese Unexamined Patent Publication No. 58-30
No. 757, JP-A No. 58-98739), alcohol-soluble nylon resin (JP-A No. 60-196766)
Publication No.), water-soluble polyvinyl butyral resin (Japanese Unexamined Patent Publication No. 6
0-232553) and polyvinyl butyral resin (Japanese Unexamined Patent Publication No. 106549/1982).
しかしながら、繰返し使用による帯電性、電荷保持性の
低下について、感光体側の改善手段では、充分な感光体
は得られていなかった。However, with regard to the deterioration of chargeability and charge retention due to repeated use, improvement measures on the photoreceptor side have not been sufficient to provide a photoreceptor.
特開昭51−111338号公報には、As、Ss、感
光体を、室温より10〜30%高く、40℃を超えない
温度に維持すると疲労(暗減衰)の速度が緩速化される
ことが開示されいてる。JP-A-51-111338 discloses that if As, Ss, and a photoreceptor are maintained at a temperature 10 to 30% higher than room temperature and not exceeding 40°C, the rate of fatigue (dark decay) will be slowed down. is disclosed.
他方、複写装置の使用環境においても、高温高湿度下で
は1画像ボケ、画像ウスなどを生じ、また、低温時にお
いては、感光体の結露、地汚れ等の問題を有しいている
。On the other hand, in the operating environment of a copying apparatus, under high temperature and high humidity conditions, single image blurring, image distortion, etc. occur, and at low temperatures, there are problems such as dew condensation on the photoreceptor and scumming.
この環境依存性に関して、特開昭61−7843号公報
には、感光層の支持体を面状発熱体として、比較的低温
で加熱すると、高温高湿下における感光体の相対湿度を
減少できることが、また特開昭62−121483号公
報には感光体に温風、冷風をふきつける方法が開示され
ており、低温時の感光体への結露防止、高温時の感光体
の劣化を防止できる方法が開示されているが、必ずしも
満足すべき方法ではなかった。特に感光層の上に保護層
を設けた高耐久化電子写真感光体を用いた場合にはその
傾向が強く更なる改善が強く望まれていた。Regarding this environmental dependence, JP-A-61-7843 discloses that the relative humidity of the photoreceptor under high temperature and high humidity can be reduced by heating the support of the photoreceptor layer at a relatively low temperature using a planar heating element. , JP-A-62-121483 discloses a method of blowing hot or cold air onto a photoreceptor, which is a method that can prevent dew condensation on the photoreceptor at low temperatures and prevent deterioration of the photoreceptor at high temperatures. has been disclosed, but the method was not necessarily satisfactory. This tendency is particularly strong when a highly durable electrophotographic photoreceptor in which a protective layer is provided on the photosensitive layer is used, and further improvements have been strongly desired.
本発明は、高温高湿度下での相対湿度を下げ画像ボケ、
画像ウスを防止できるとともに低温時の感光体の結露防
止及び低温湿度下での地汚れを防止し得る電子写真プロ
セスを提供することを目的とする。The present invention reduces relative humidity under high temperature and high humidity conditions and reduces image blur.
An object of the present invention is to provide an electrophotographic process that can prevent image distortion, dew condensation on a photoreceptor at low temperatures, and background smear at low temperatures and humidity.
本発明によれば、導電性支持体上に少なくとも感光層を
設けてなる電子写真感光体を帯電、露光し静電潜像を形
成する工程を含む電子写真プロセスにおいて、該感光体
を常に50℃以上に保持することを特徴とする電子写真
プロセスが提供される。According to the present invention, in an electrophotographic process including a step of charging and exposing an electrophotographic photoreceptor having at least a photosensitive layer on a conductive support to form an electrostatic latent image, the photoreceptor is always kept at 50°C. Provided is an electrophotographic process characterized by the above-mentioned retention.
本発明者らは、導電性支持体上に少なくとも感光層を設
けてなる電子写真感光体の有する従来の欠点を解消すべ
く検討した結果、電子写真感光体を常時50℃以上に保
持するプロセスを採用するならば、これらの欠陥が克服
できることを知見し、本発明を完成するに到った。The inventors of the present invention have conducted studies to solve the conventional drawbacks of electrophotographic photoreceptors in which at least a photosensitive layer is provided on a conductive support. The present inventors have found that these defects can be overcome if the present invention is adopted, and have completed the present invention.
本発明者らの研究によれば、電子写真感光体の使用時に
おいて、常に感光体を少なくとも50℃以上に加温して
おくと繰り返し使用によっても、初期と同じ程度の感光
体特性が発現することが知見された。この場合、加温す
る温度の上限は特に限定されないが、高温で加温する場
合は感光層中の有機物質が増化等の変質を生じたり、現
像部のトナーの融解、固着等を引き起こすため、本発明
における上限の加温温度、感光体、トナー等の構成材料
によって多少の差異はあるが、好ましくは100℃以下
、更に好ましくは80℃以下とすることが望ましい。According to research by the present inventors, when using an electrophotographic photoreceptor, if the photoreceptor is always heated to at least 50°C or higher, the same level of photoreceptor characteristics as the initial one will be developed even after repeated use. It was discovered that In this case, the upper limit of the heating temperature is not particularly limited, but heating at a high temperature may cause deterioration such as increase in organic substances in the photosensitive layer, or may cause melting or sticking of toner in the developing area. Although there are some differences depending on the upper limit heating temperature in the present invention and the constituent materials such as the photoreceptor and toner, it is preferably 100° C. or lower, and more preferably 80° C. or lower.
また、加温手段としては、電気抵抗加熱器(特開昭51
−111338号公報)、暖気を吹き付ける方法(特開
昭51−111338号公報、特開昭62−12148
2号公報)、支持体として面状発熱体を用いる(特開昭
61−7843号公報)、また支持体内側に面状発熱体
を貼り付ける等の手段が挙げられるが、これに限定され
ることはない。In addition, as a heating means, an electric resistance heater (Unexamined Japanese Patent Publication No. 51
-111338 Publication), a method of blowing warm air (Japanese Patent Application Laid-open No. 51-111338, Japanese Patent Application Laid-Open No. 62-12148)
2), using a sheet heating element as a support (Japanese Unexamined Patent Publication No. 61-7843), and pasting a sheet heating element on the inside of the support, but are not limited to these. Never.
本発明の電子写真プロセスは前記構成からなるものであ
るが、別の構成として上記構成要件に加えて冷却手段と
、冷却手段の作動手段を用いてもよい。即ち、必要温度
以上に感光体が加温された場合、あるいは加熱された感
光体を使用時に所定温度まで冷却する場合に、冷却手段
はを採用することは有用である。この場合の冷却手段と
しては、冷却空気を吹き付ける(特開昭62−1214
82号公報)、冷媒を用いる方法等が挙げられるがこれ
らに限定されることはない。Although the electrophotographic process of the present invention has the above configuration, a cooling means and an actuation means for the cooling means may be used in addition to the above configuration as another configuration. That is, it is useful to employ the cooling means when the photoreceptor is heated above a required temperature or when the heated photoreceptor is cooled to a predetermined temperature during use. In this case, the cooling means is to blow cooling air (Japanese Patent Laid-Open No. 62-1214
82), a method using a refrigerant, etc., but the method is not limited thereto.
上記の加温手段および冷却手段は感光体の内側に着装し
てもよく、同時に/あるいは感光体外側の適当な位置に
1個以上着装してもよい。The above-mentioned heating means and cooling means may be installed inside the photoreceptor, and/or one or more of them may be installed at appropriate positions outside the photoreceptor at the same time.
次に図面によって本発明で用いる電子写真感光体を説明
する。Next, the electrophotographic photoreceptor used in the present invention will be explained with reference to the drawings.
第1図は、本発明において使用する感光体の構成例を示
す断面図であり、導電性支持体11上に、感光層14を
設けたものである。FIG. 1 is a cross-sectional view showing an example of the structure of a photoreceptor used in the present invention, in which a photoreceptor layer 14 is provided on a conductive support 11. As shown in FIG.
第2図a、第2図すは、別の構成例を示す断面図であり
感光層が電荷発生層21と、電荷輸送M22との積層で
構成されている。FIGS. 2A and 2S are cross-sectional views showing another example of the structure, in which the photosensitive layer is composed of a stack of a charge generation layer 21 and a charge transport M22.
第3図は、更に別の構成例であって導電性支持体11と
感光Jt!14の間に下引層15を設けたものである。FIG. 3 shows yet another example of the structure, in which the conductive support 11 and the photosensitive Jt! A subbing layer 15 is provided between the layers 14.
第4図は第1図の感光層14の上に保ff層12を設け
たものであり、第5図は第4図において感光層14と保
護層12の間に中間M13を設けたものである。4 shows a structure in which an FF retention layer 12 is provided on the photosensitive layer 14 in FIG. 1, and FIG. 5 shows a structure in which an intermediate M13 is provided between the photosensitive layer 14 and the protective layer 12 in FIG. be.
第6図a及び第6図すは各々第2図a及び第2図すの上
に保W /ff 12を設けたものである。FIGS. 6a and 6s are respectively the same as FIGS.
第7図は第4図において導電性支持体11と感光層14
の間に下引層15を設けたものである。FIG. 7 shows the conductive support 11 and the photosensitive layer 14 in FIG.
A subbing layer 15 is provided in between.
導電性基体11としては、体積抵抗1010Ω1以下の
導電性を示すもの、例えば、アルミニウム、ニッケル、
クロム、ニクロム、銅、銀、金、白金などの金属、酸化
スズ、酸化インジウムなどの金属酸化物を、蒸着又はス
パッタリングにより、フィルム状もしくは円筒状のプラ
スチック、紙に被覆したもの、あるいは、アルミニウム
、アルミニウム合金、ニッケル、ステンレス等の板およ
びそれらをり、、1.1.、押出し、引抜き等の工法で
素管化後。The conductive substrate 11 may be one that exhibits conductivity with a volume resistance of 1010Ω1 or less, such as aluminum, nickel,
Metals such as chromium, nichrome, copper, silver, gold, and platinum, and metal oxides such as tin oxide and indium oxide are coated on film or cylindrical plastic or paper by vapor deposition or sputtering, or aluminum, Plates of aluminum alloy, nickel, stainless steel, etc. and their materials, 1.1. , after making it into a blank pipe using extrusion, drawing, etc. methods.
切削、超仕上げ、研摩等で表面処理した管等を使用する
ことができる。A pipe or the like whose surface has been treated by cutting, superfinishing, polishing, etc. can be used.
本発明における感光層14は、無機系、有機系のいずれ
もが使用でき、無機系感光層としては、たとえば無定形
Ss、 5e−Te化合物、5a−As化合物、5s−
Te−CD化合物、CdS、ZnO等が挙げられる。The photosensitive layer 14 in the present invention can be either inorganic or organic. Examples of the inorganic photosensitive layer include amorphous Ss, 5e-Te compound, 5a-As compound, 5s-
Examples include Te-CD compounds, CdS, ZnO, and the like.
次に有機系感光層14について説明するが、先ず積層感
光層について述べる。Next, the organic photosensitive layer 14 will be explained, but first, the laminated photosensitive layer will be described.
電荷発生層21は、電荷発生物質を主材料とした層で、
必要に応じてバインダー樹脂を用いることもある。The charge generation layer 21 is a layer mainly made of a charge generation substance,
A binder resin may be used if necessary.
バインダー樹脂としては、ポリアミド、ポリウレタン、
ポリエステル、エポキシ樹脂、ポリケトン、ポリカーボ
ネート、シリコーン樹脂、アクリル樹脂、ポリビニルブ
チラール、ポリビニルホルマール、ポリビニルケトン、
ポリスチレン、ポリ−N−ビニルカルバゾール、ポリア
クリルアミドなどが用いられる。Binder resins include polyamide, polyurethane,
Polyester, epoxy resin, polyketone, polycarbonate, silicone resin, acrylic resin, polyvinyl butyral, polyvinyl formal, polyvinyl ketone,
Polystyrene, poly-N-vinylcarbazole, polyacrylamide, etc. are used.
電荷発生物質としては、例えば、シーアイピグメントブ
ルー25〔カラーインデックス(CI)21180)、
シーアイピグメントレッド41(CI 21200)、
シーアイアシッドレッド52(CI 45100)、シ
ーアイベーシックレッド3(CI 45210)、さら
に、ポルフィリン骨格を有するフタロシアニン系顔料、
カルバゾール骨格を有するアゾ顔料(特開昭53−95
033号公報に記載)、ジスチリルベンゼン骨格を有す
るアゾ顔料(特開昭53−133455号公報に記載)
、トリフェニルアミン骨格を有するアゾ顔料(特開昭5
3−132547号公報に記載)、ジベンゾチオフェン
骨格を有するアゾ顔料(特開昭54−21728号公報
に記載)、オキサジアゾール骨格を有するアゾ顔料(特
開昭54−12742号公報に記載)、フルオレノン骨
格を有するアゾ顔料(特開昭54−22834号公報に
記載)、ビススチルベン骨格を有するアゾ顔料(特開昭
54−17733号公報に記載)、ジスチリルオキサジ
アゾール骨格を有するアゾ顔料(特開昭54−2129
号公報に記載)、ジスチリルカルバゾール骨格を有する
アゾ顔料(特開昭54−17734号公報に記載)、さ
らに、シーアイピグメントブルー16(CI 7410
0)等のフタ口シアニン系顔料、シーアイバットブラウ
ン5(CI 73410)、シーアイバットダイ(CI
73030)等のインジゴ系顔料、アルゴスカーレッ
トB(バイオレット社製)、インダンスレンスカーレッ
トR(バイエル社製)等のペリレン系顔料などが挙げら
れる。Examples of the charge generating substance include CI Pigment Blue 25 [Color Index (CI) 21180],
CI Pigment Red 41 (CI 21200),
C.I. Acid Red 52 (CI 45100), C.I. Basic Red 3 (CI 45210), and a phthalocyanine pigment having a porphyrin skeleton,
Azo pigments having a carbazole skeleton (JP-A-53-95)
033), an azo pigment having a distyrylbenzene skeleton (described in JP-A-53-133455)
, an azo pigment having a triphenylamine skeleton (Japanese Unexamined Patent Publication No. 5
3-132547), an azo pigment having a dibenzothiophene skeleton (described in JP-A-54-21728), an azo pigment having an oxadiazole skeleton (described in JP-A-54-12742), Azo pigments having a fluorenone skeleton (described in JP-A No. 54-22834), azo pigments having a bisstilbene skeleton (described in JP-A-54-17733), azo pigments having a distyryloxadiazole skeleton ( Japanese Patent Publication No. 54-2129
Azo pigments having a distyrylcarbazole skeleton (described in JP-A-54-17734), CI Pigment Blue 16 (CI 7410)
0), C.I. Butt Brown 5 (CI 73410), C.I. Butt Dye (CI
73030), and perylene pigments such as Argo Scarlet B (manufactured by Violet) and Indance Scarlet R (manufactured by Bayer).
これら電荷発生物質の中でも、アゾ顔料が好適である。Among these charge generating substances, azo pigments are preferred.
これらの電荷発生物質は、単独で、あるいは2種以上併
用して用いられる。These charge generating substances may be used alone or in combination of two or more.
バインダー樹脂は、電荷発生物質100重量部に対して
0〜100重量部用いるのが適当であり、好ましくは0
〜50重量部である。The binder resin is suitably used in an amount of 0 to 100 parts by weight, preferably 0 to 100 parts by weight, based on 100 parts by weight of the charge generating substance.
~50 parts by weight.
電荷発生層は、電荷発生物質を必要ならばバインダー樹
脂とともに、テトラヒドロフラン、シクロヘキサン、ジ
オキサン、ジクロルエタン等の溶媒を用いてボールミル
、アトライター、サンドミルなどにより分散し、分散液
を適度に希釈して塗布することにより形成できる。塗布
は、浸漬塗工法やスプレーコート、ビードコート法など
を用いて行なうことができる。The charge generation layer is prepared by dispersing a charge generation substance together with a binder resin if necessary using a ball mill, attritor, sand mill, etc. using a solvent such as tetrahydrofuran, cyclohexane, dioxane, dichloroethane, etc., diluting the dispersion liquid appropriately and applying it. It can be formed by Application can be performed using a dip coating method, a spray coating method, a bead coating method, or the like.
電荷発生層の膜厚は、0.01〜5μ備程度が適当であ
り、好ましくは0.1〜2−である。The thickness of the charge generation layer is suitably about 0.01 to 5 μm, preferably 0.1 to 2 μm.
電荷輸送層22は、電荷輸送物質およびバインダー樹脂
を適当な溶剤に溶解ないし分散し、これを電荷発生層上
に塗布、乾燥することにより形成できる。また、必要に
より可塑剤やレベリング剤等を添加することもできる。The charge transport layer 22 can be formed by dissolving or dispersing a charge transport substance and a binder resin in a suitable solvent, coating the solution on the charge generation layer, and drying the solution. Moreover, a plasticizer, a leveling agent, etc. can also be added if necessary.
電荷輸送物質には、正孔輸送物質と電子輸送物質とがあ
る。Charge transport materials include hole transport materials and electron transport materials.
正孔輸送物質としては、ポリ−N−ビニルカルバゾール
およびその誘導体、ポリーγ−カルバゾリルエチルグル
タメートおよびその誘導体、ピレン−ホルムアルデヒド
縮金物およびその誘導体、ポリビニルピレン、ポリビニ
ルフェナントレン、ポリビニルピレン、オキサゾール誘
導体、オキサジアゾール誘導体、イミダゾール誘導体、
トリフェニルアミン誘導体、9−(P−ジエチルアミノ
スチリル)アントラセン、1,1−ビス−(4−ジベン
ジルアミノフェニル)プロパン、スチリルアントラセン
、スチリルピラゾリン、フェニルヒドラゾン類、α−フ
ェニルスチルベン誘導体、ベンジジン誘導体等の電子供
与性物質が挙げられる。As hole transport substances, poly-N-vinylcarbazole and its derivatives, poly-γ-carbazolylethyl glutamate and its derivatives, pyrene-formaldehyde condensate and its derivatives, polyvinylpyrene, polyvinylphenanthrene, polyvinylpyrene, oxazole derivatives, Oxadiazole derivatives, imidazole derivatives,
Triphenylamine derivatives, 9-(P-diethylaminostyryl)anthracene, 1,1-bis-(4-dibenzylaminophenyl)propane, styrylanthracene, styrylpyrazoline, phenylhydrazones, α-phenylstilbene derivatives, benzidine derivatives Electron-donating substances such as
電子輸送物質としては、たとえば、クロルアニル、ブロ
ムアニル、テトラシアノエチレン、テトラシアノキノン
ジメタン、2,4.7−ドリニトロー9−フルオレノン
、2,4,5.7−テトラニトロ−9−フルオレノン、
2,4,5.7−チトラニトロキサントン、2.4.8
−トリニドロチオキサントン、2,6.8−トリニトロ
−4H−インデノ(1,2−b)チオフェン−4−オン
、1.3.7− トリニトロジベンゾチオフェン−5,
5−ジオキサイドなどの電子受容性物質が挙げられる。Examples of the electron transport substance include chloranil, bromoanil, tetracyanoethylene, tetracyanoquinone dimethane, 2,4,7-dolinitro-9-fluorenone, 2,4,5,7-tetranitro-9-fluorenone,
2,4,5.7-titranitroxanthone, 2.4.8
-trinidrothioxanthone, 2,6.8-trinitro-4H-indeno(1,2-b)thiophen-4-one, 1.3.7-trinitrodibenzothiophene-5,
Examples include electron-accepting substances such as 5-dioxide.
これらの電荷輸送物質は、単独又は2種以上混合して用
いられる。These charge transport substances may be used alone or in a mixture of two or more.
バインダー樹脂としてはポリスチレン、スチレン−アク
リロニトリル共重合体、スチレン−ブタジェン共重合体
、スチレン−無水マレイン酸共重合体、ポリエステル、
ポリ塩化ビニル、塩化ビニル−酢酸ビニル共重合体、ポ
リ酢酸ビニル、ポリ塩化ビニリデン、ポリアクリレート
樹脂、フェノキシ樹脂、ポリカーボネート、酢酸セルロ
ース樹脂、エチルセルロース樹脂、ポリビニルブチラー
ル、ポリビニルホルマール、ポリビニルトルエン、ポリ
−N−ビニルカルバゾール、アクリル樹脂、シリコーン
樹脂、エポキシ樹脂、メラミン樹脂、ウレタン樹脂、フ
ェノール樹脂、アルキッド樹脂等の熱可塑性または熱硬
化性樹脂が挙げられる。Binder resins include polystyrene, styrene-acrylonitrile copolymer, styrene-butadiene copolymer, styrene-maleic anhydride copolymer, polyester,
Polyvinyl chloride, vinyl chloride-vinyl acetate copolymer, polyvinyl acetate, polyvinylidene chloride, polyacrylate resin, phenoxy resin, polycarbonate, cellulose acetate resin, ethyl cellulose resin, polyvinyl butyral, polyvinyl formal, polyvinyl toluene, poly-N- Examples include thermoplastic or thermosetting resins such as vinyl carbazole, acrylic resin, silicone resin, epoxy resin, melamine resin, urethane resin, phenol resin, and alkyd resin.
溶剤としては、テトラヒドロフラン、ジオキサン、トル
エン、モノクロルベンゼン、ジクロルエタン、塩化メチ
レンなどが用いられる。As the solvent, tetrahydrofuran, dioxane, toluene, monochlorobenzene, dichloroethane, methylene chloride, etc. are used.
電荷輸送層22の厚さは、5〜50−程度が適当である
。The thickness of the charge transport layer 22 is suitably about 5 to 50 mm.
次に感光層14が単層構成の場合について述べる。Next, a case where the photosensitive layer 14 has a single layer structure will be described.
この場合も多くは電荷発生物質と電荷輸送物質よりなる
機能分離型のものが挙げられる。In this case as well, most of the materials are of a functionally separated type consisting of a charge generating substance and a charge transporting substance.
即ち、電荷発生物質および電荷輸送物質には先に示した
化合物を用いることができる。That is, the compounds shown above can be used as the charge generating substance and the charge transporting substance.
単層感光層は、電荷発生物質および電荷輸送物質および
バインダー樹脂を適当な溶剤に溶解ないし分散し、これ
を塗布、乾燥することによって形成できる。また、必要
により可塑剤やレベリング剤等を添加することもできる
。A single-layer photosensitive layer can be formed by dissolving or dispersing a charge generating substance, a charge transporting substance and a binder resin in a suitable solvent, coating the solution and drying the solution. Moreover, a plasticizer, a leveling agent, etc. can also be added if necessary.
バインダー樹脂としては、先に電荷輸送層22で挙げた
バインダー樹脂をそのまま用いるほかに、電荷発生層2
1で挙げたバインダー樹脂を混合して用いてもよい。As the binder resin, in addition to using the binder resin mentioned above for the charge transport layer 22 as is, the binder resin for the charge generation layer 2
The binder resins listed in 1 may be used in combination.
単層感光層は、電荷発生物質、電荷輸送物質およびバイ
ンダー樹脂をテトラヒドロフラン、ジオキサン、ジクロ
ルエタン、シクロヘキサノン等の溶媒を用いて分散機等
で分散した塗工液を浸漬塗工法やスプレーコート、ビー
ドコートなどで塗工して形成できる。The single-layer photosensitive layer is formed by dipping coating, spray coating, bead coating, etc. using a coating solution in which a charge generating substance, a charge transporting substance, and a binder resin are dispersed using a dispersion machine using a solvent such as tetrahydrofuran, dioxane, dichloroethane, or cyclohexanone. Can be formed by coating.
単層感光層の膜厚は、5〜50.程度が適当である。The thickness of the single photosensitive layer is 5 to 50. The degree is appropriate.
なお、本発明において感光層14の上にさらに絶a層を
設けることも可能である。In the present invention, it is also possible to further provide an ablation layer on the photosensitive layer 14.
また、本発明において第5図に示されるように、導電性
支持体と、感光層との間に中間層13を設けることによ
り1本発明の効果をいっそう向上させることが可能であ
り、また接着性を改良することもできる。Further, in the present invention, as shown in FIG. 5, by providing an intermediate layer 13 between the conductive support and the photosensitive layer, it is possible to further improve the effects of the present invention, and You can also improve your gender.
中間層13には、S10. AatOa等の無機材料を
蒸着、スパッタリング、陽極酸化などの方法で設けたも
のや、ポリアミド樹脂(特開昭58−30757号公報
、特開昭58−98739号公報)5アルコール可溶性
ナイロン樹脂(特開昭60−196766号公報)、水
溶性ポリビニルブチラール樹脂(特開昭60−2325
53号公報)、ポリビニルブチラール樹脂(特開昭58
−106549号公報)、ポリビニルアルコールなどの
樹脂層を用いることができる。The intermediate layer 13 includes S10. Those in which inorganic materials such as AatOa are applied by vapor deposition, sputtering, anodization, etc., polyamide resins (JP-A-58-30757, JP-A-58-98739) and alcohol-soluble nylon resin (JP-A-58-98739). Publication No. 60-196766), water-soluble polyvinyl butyral resin (Japanese Unexamined Patent Publication No. 60-2325)
No. 53), polyvinyl butyral resin (Japanese Unexamined Patent Publication No. 58
106549), a resin layer made of polyvinyl alcohol, etc. can be used.
また、上記樹脂中間層にZnO,TiO2、ZnS等の
顔料粒子を分散したものも、中間層として用いることが
できる。Furthermore, a resin intermediate layer in which pigment particles such as ZnO, TiO2, ZnS, etc. are dispersed can also be used as the intermediate layer.
更に本発明の中間層13として、シランカップリング剤
、チタンカップリング剤、クロムカップリング剤等を使
用することもできる。Furthermore, as the intermediate layer 13 of the present invention, a silane coupling agent, a titanium coupling agent, a chromium coupling agent, etc. can also be used.
中間層13の膜厚は0〜5psが適当である。The appropriate thickness of the intermediate layer 13 is 0 to 5 ps.
保護層12に使用される樹脂としては、 ABSII!
II脂、ACS樹脂、オレフィンビニル共重合体樹脂、
塩素化ポリエーテル、アリル樹脂、フェノール樹脂、ポ
リアセタール、ポリアミド、ポリアミドイミド、ボリア
リレート、ポリアリルスルホン、ポリブチレン、ポリブ
チレンテレフタレート、ポリカーボネート、ポリエーテ
ルスルホン、ポリエチレン、ポリエチレンテレフタレー
ト、ポリイミド、メタクリル樹脂、ポリメチルペンテン
、ポリプロピレン、ポリフェニレンオキシド、ポリスル
ホン、ポリスチレン、AS樹脂、ブタジェン−スチレン
樹脂、ポリウレタン、ポリ塩化ビニル、ポリ塩化ビニリ
デン、エポキシ樹脂等が挙げられる。The resin used for the protective layer 12 is ABSII!
II fat, ACS resin, olefin vinyl copolymer resin,
Chlorinated polyether, allyl resin, phenolic resin, polyacetal, polyamide, polyamideimide, polyarylate, polyallylsulfone, polybutylene, polybutylene terephthalate, polycarbonate, polyether sulfone, polyethylene, polyethylene terephthalate, polyimide, methacrylic resin, polymethylpentene , polypropylene, polyphenylene oxide, polysulfone, polystyrene, AS resin, butadiene-styrene resin, polyurethane, polyvinyl chloride, polyvinylidene chloride, epoxy resin, and the like.
また、耐摩耗性の観点から添加剤としてポリテトラフロ
ロエチレン樹脂、フッ素系樹脂、シリコーン系樹脂を添
加し、摩耗係数を下げ、耐摩耗性並びに耐傷化性の向上
を図ることでき、また酸化チタン、酸化錫、チタン酸カ
リウムの無機化合物を前記樹脂中に分散しても耐摩耗性
が向上する。In addition, from the viewpoint of wear resistance, polytetrafluoroethylene resin, fluorine resin, and silicone resin can be added as additives to lower the wear coefficient and improve wear resistance and scratch resistance. The wear resistance can also be improved by dispersing inorganic compounds such as , tin oxide, and potassium titanate into the resin.
この表面保護層の膜厚は0.5−10.、好ましくは1
〜5psである。The thickness of this surface protective layer is 0.5-10. , preferably 1
~5 ps.
また、本発明においては第3図及び第7図に示されるよ
うに導電性支持体llと感光層14の間に下引層15を
設けることもできる。この場合、下引層を形成する樹脂
として中間層で用いられる樹脂がそのまま適用される。Furthermore, in the present invention, as shown in FIGS. 3 and 7, a subbing layer 15 can be provided between the conductive support 11 and the photosensitive layer 14. In this case, the resin used in the intermediate layer is used as is as the resin forming the undercoat layer.
次に実施例によって本発明を更に詳しく説明するが1本
発明は以下の実施例に限定されるものではない。Next, the present invention will be explained in more detail with reference to examples, but the present invention is not limited to the following examples.
実施例1
外径40m+a、長さ250mmのアルミニウムシリン
ダー上に、下記組成の電荷発生層塗工液、電荷輸送層塗
工液を塗布、乾燥し電荷発生層(0,1μs)、電荷輸
送層(20μ、)を形成した。Example 1 On an aluminum cylinder with an outer diameter of 40 m+a and a length of 250 mm, a charge generation layer coating liquid and a charge transport layer coating liquid having the following compositions were applied and dried to form a charge generation layer (0.1 μs) and a charge transport layer ( 20μ,) was formed.
下記構造式のトリスアゾ顔料 2重量部シクロヘ
キサノン 70〃メチルエチルケ
トン 28〃[電荷輸送層塗工液〕
下記構造式の電荷輸送物質 10重量部テトラ
ヒドロフラン 80〃以上の様に作成し
た有機感光体を、レーザープリンター(リコーpcレー
ザー6000)に塔載し、帯電直後の感光体の表面電位
が測定できる位置に表面電位計のプローブをセットした
。また、感光体加温用のヒーターはアルミニウムドラム
の内側に発熱体を貼りつけ、ドラム温度が25℃(室温
)、40℃、45℃、50℃、60℃、70℃になるよ
うにコントロールした。各条件をセットした後、レーザ
ープリンターを繰り返し使用し、現像直前の非露光部の
表面電位を測定した。Trisazo pigment with the following structural formula: 2 parts by weight Cyclohexanone 70〃Methyl ethyl ketone 28〃[Charge transport layer coating liquid] Charge transport material with the following structural formula: 10 parts by weight Tetrahydrofuran 80〃The organic photoreceptor prepared as above was printed using a laser printer ( The probe of the surface electrometer was set at a position where the surface potential of the photoreceptor immediately after charging could be measured. In addition, the heater for heating the photoreceptor was a heating element attached to the inside of the aluminum drum, and the drum temperature was controlled to be 25°C (room temperature), 40°C, 45°C, 50°C, 60°C, and 70°C. . After setting each condition, the laser printer was used repeatedly and the surface potential of the unexposed area immediately before development was measured.
第8図に3000枚時の表面電位と感光体温度の関係を
示す(初期は一800V)。FIG. 8 shows the relationship between the surface potential and the photoreceptor temperature after 3,000 sheets were printed (-800 V at the initial stage).
第8図から、繰り返し使用を行なっても50℃以上の領
域においては非露光部の表面電位の低下が少なく、経時
による帯電特性の劣化が有効に防止されていることが判
る。From FIG. 8, it can be seen that even after repeated use, there is little decrease in the surface potential of the non-exposed area in the region of 50° C. or higher, and deterioration of charging characteristics over time is effectively prevented.
実施例2
〔電荷発生層塗工液〕
X型無金属フタロシアニン 10重量部シクロ
へキサノン 185重量部からなる組
成物をボールミルで48時間分散、混合して電荷発生層
塗工液を得た。この塗工液を、アルミニウム導電層を有
するポリエステルフィルム支持体上に塗布、乾燥して膜
厚0.2IJmの電荷発生層を形成した。この上に以下
の組成の電荷輸送層塗工液を塗布乾燥し、膜厚20μs
の電荷輸送層を形成して電子写真感光体を作成した。Example 2 [Charge generation layer coating liquid] A composition consisting of 10 parts by weight of X-type metal-free phthalocyanine and 185 parts by weight of cyclohexanone was dispersed and mixed in a ball mill for 48 hours to obtain a charge generation layer coating liquid. This coating solution was applied onto a polyester film support having an aluminum conductive layer and dried to form a charge generating layer having a thickness of 0.2 IJm. On top of this, a charge transport layer coating solution with the following composition was applied and dried, and the film thickness was 20 μs.
An electrophotographic photoreceptor was prepared by forming a charge transport layer.
下記構造式の電荷輸送物質 10重量部テトラ
ヒドロフラン 80重量部次に、この電
子写真感光体に導電層塗工およびベルト接合を行ない、
ついで、温風空気を吹きつけられる様な装置をつけられ
るべく改造を行なって、実装用の感光体とした。レーザ
ープリンター(リコーLP−4080)に塔載した。こ
のレーザープリンターを(10℃、40%)、(25℃
、45%)及び(25℃、90%)の環境下にて繰り返
し使用を行ない、3000枚目の画像を評価した。尚感
光体温度は50℃に保った。結果を表−1に示す。A charge transport material having the following structural formula: 10 parts by weight Tetrahydrofuran: 80 parts by weight Next, this electrophotographic photoreceptor was coated with a conductive layer and bonded with a belt,
Next, we modified it so that it could be equipped with a device that could blow warm air onto it, and used it as a photoreceptor for mounting. It was loaded onto a laser printer (Ricoh LP-4080). This laser printer (10℃, 40%), (25℃
, 45%) and (25° C., 90%), and the 3000th image was evaluated. The temperature of the photoreceptor was maintained at 50°C. The results are shown in Table-1.
比較例1
感光体温度を50℃に保つ操作をしない他は実施例2と
同様の評価を行なった。結果を表−1に示す。Comparative Example 1 Evaluation was conducted in the same manner as in Example 2, except that the photoreceptor temperature was not maintained at 50°C. The results are shown in Table-1.
表−1 0;濃度低下及び地汚れが認められない。Table-1 0: No decrease in density or background staining observed.
Δ;濃度低下が認められないが地汚れが顕著となる。Δ: No decrease in density is observed, but background staining becomes noticeable.
X;濃度低下が著しく、また地汚れも顕著となる。X: Density decreases significantly, and background stains also become noticeable.
実施例3
〔電荷発生層塗工液〕
ポリビニルブチラール樹脂 2重量部シクロヘ
キサノン 120重量部シクロヘキサ
ン 60重量部からなる組成物をボ
ールミルで48時間、分散、混合して電荷発生層塗工液
を得た。これを外径80mm、長さ340mmのアルミ
ニウムドラムに下引層として、ポリアミド樹脂を塗工し
たもの(0,3μff1)の上に約0゜1μl塗工した
。Example 3 [Charge generation layer coating liquid] A composition consisting of 2 parts by weight of polyvinyl butyral resin, 120 parts by weight of cyclohexanone, and 60 parts by weight of cyclohexane was dispersed and mixed in a ball mill for 48 hours to obtain a charge generation layer coating liquid. This was applied as a subbing layer to an aluminum drum having an outer diameter of 80 mm and a length of 340 mm, and approximately 0.1 μl of this was coated on top of the polyamide resin coating (0.3 μff1).
(下引用塗工液〕
メタノール 96重社部更にこ
の上に以下の組成からなる電荷輸送層用の塗工液で20
pI11塗工し、感光体を得た。(Coating liquid quoted below) Methanol 96 Jyushabu Further on top of this, apply a coating liquid for the charge transport layer having the following composition.
A photoreceptor was obtained by coating pI11.
下記構造式の電荷輸送物質 10重社部塩化メ
チレン 80重量部以上の様に作
成した感光体を複写機リコピーFT551Oを負帯電す
る様に改造したものにセットし、実施例2と同様な温風
吹き付は装置をセットし、実施例1と同様な方法で現像
直前の非露光部の表面電位を測定した。感光体温度は5
5℃に保ちながらコピー5000枚までくり返し使用を
行った〔なお、条件は室温(25℃、45%)下で行な
った〕。結果を第9図に示す。Charge transport material having the following structural formula: 10 parts methylene chloride 80 parts by weight or more The photoreceptor prepared as above was set in a copying machine Ricopy FT551O modified to be negatively charged, and heated with hot air as in Example 2. For spraying, the apparatus was set, and the surface potential of the non-exposed area immediately before development was measured in the same manner as in Example 1. Photoreceptor temperature is 5
It was repeatedly used for up to 5,000 copies while maintaining the temperature at 5°C [note that the conditions were room temperature (25°C, 45%)]. The results are shown in Figure 9.
比較例2
感光体温度を制御せずに繰り返し使用した他は実施例3
全く同じ評価をした。結果を第9図に記す。Comparative Example 2 Same as Example 3 except that the photoreceptor temperature was repeatedly used without controlling it.
I gave the exact same evaluation. The results are shown in Figure 9.
実施例4
直径80mm、長さ340mmのアルミニウムドラム上
に、下記組成からなる電荷輸送層を20μa+塗工した
。Example 4 On an aluminum drum having a diameter of 80 mm and a length of 340 mm, a charge transport layer having the following composition was coated in an amount of 20 μa.
テトラヒドロフラン 80重量部モノク
ロロベンゼン 80重量部しh3
この上に下記組成からなる電荷発生層を約2声塗工した
。Tetrahydrofuran: 80 parts by weight Monochlorobenzene: 80 parts by weight h3 Approximately two charge generation layers having the following composition were coated thereon.
ポリビニルブチラール樹脂 4重量部シクロへ
キサノン 120重量部メチルイソブ
チルケトン 60重量部以上の様にスプレー
コーティングにより作成した感光体を複写機リコピーF
T5510にセットし、実施例2と同様な温風吹き付は
装置を塔載し、実施例2と同じ環境条件にて画像評価を
行なった(温度は60℃)。Polyvinyl butyral resin: 4 parts by weight Cyclohexanone: 120 parts by weight Methyl isobutyl ketone: 60 parts by weight or more
T5510 was set, a hot air blowing device similar to that in Example 2 was installed, and image evaluation was performed under the same environmental conditions as in Example 2 (temperature: 60° C.).
4000枚時の画像サンプルを評価した結果、実施例4
の場合の画像は、ボケ、地よごれのない鮮明な画像が得
られたが、施さない場合には低温時の地よごれ、高湿時
のボケが発生した。As a result of evaluating image samples after 4000 sheets, Example 4
In the case of , clear images with no blurring or background stains were obtained, but in the case of no application, background stains occurred at low temperatures and blurring at high humidity.
実施例5
実施例1で用いた感光体の有機感光層の上に下記組成か
らなる保護層塗工液を4μ閣塗工した。Example 5 On the organic photosensitive layer of the photoreceptor used in Example 1, 4μ of a protective layer coating solution having the following composition was coated.
導電性チタン(三菱金属社製)100重量部トルエン
240重斌部ブタノール
60重量部以上の液を混合した
後、ボールミルで72時間分散した後、トルエン/ブタ
ノール=4/l(重電比)になるように固形分濃度1%
に希釈したもの。Conductive titanium (manufactured by Mitsubishi Metals) 100 parts by weight toluene
240 parts butanol
After mixing 60 parts by weight or more of the liquid and dispersing it in a ball mill for 72 hours, the solid content concentration is 1% so that toluene/butanol = 4/l (heavy electric ratio).
diluted with.
以上の様に作成した感光体を実施例1と同様なレーザー
プリンターに塔載し、実施例1と同じ条件でプリントし
た。第1O図に3000枚時の表面電位と感光体温度の
関係を示す(初期は一800V)。The photoreceptor prepared as described above was placed on a laser printer similar to that in Example 1, and printed under the same conditions as in Example 1. FIG. 1O shows the relationship between the surface potential and the photoreceptor temperature when 3000 sheets were printed (initially -800 V).
第10図からも判る様に、繰り返し使用を行なっても、
50℃以上の領域においては、非露光部の表面電位の低
下が少なく、経時により帯電特性の劣化が有効に防止さ
れている事が判る。As can be seen from Figure 10, even after repeated use,
It can be seen that in the temperature range of 50° C. or higher, the surface potential of the non-exposed area decreases little, and deterioration of the charging characteristics over time is effectively prevented.
実施例6
実施例2で用いた感光体の有機感光層の上に実施例5で
使用した保護層塗工液を約3p塗工した以外は実施例2
と同様にして電子写真感光体を作成した。ついで、この
感光体を用いて実施例2と同様なプリント試験を行なっ
た。その結果を表−2に示す。Example 6 Example 2 except that about 3p of the protective layer coating solution used in Example 5 was applied on the organic photosensitive layer of the photoreceptor used in Example 2.
An electrophotographic photoreceptor was prepared in the same manner as described above. Next, a printing test similar to that in Example 2 was conducted using this photoreceptor. The results are shown in Table-2.
比較例3
感光体温度を50℃に保つ操作をしない他は実施例6と
同様な評価を行なった。結果を表−2に示す。Comparative Example 3 Evaluation was conducted in the same manner as in Example 6, except that the photoreceptor temperature was not maintained at 50°C. The results are shown in Table-2.
表−2 *;画像が発現しない。Table-2 *: No image appears.
実施例7
実施例3において、感光層の上に実施例5と同じ保護層
塗工液を4μm塗工した以外は実施例3と同様にして電
子写真感光体を作成した。ついでこの感光体を用いて実
施例3と同様な条件でコピーを行なった。その結果を第
11図に示す。Example 7 An electrophotographic photoreceptor was prepared in the same manner as in Example 3, except that the same protective layer coating solution as in Example 5 was coated on the photosensitive layer to a thickness of 4 μm. Copying was then carried out using this photoreceptor under the same conditions as in Example 3. The results are shown in FIG.
比較例4
実施例6において、感光体温度を制御せずに繰り返し使
用した他は全く同じ評価をした。その結果を第11図に
示す。Comparative Example 4 The same evaluation as in Example 6 was carried out except that the photoreceptor temperature was not controlled and the photoreceptor was used repeatedly. The results are shown in FIG.
実施例8
実施例4において、電荷発生層の上に下記組成からなる
中間層0.3μmを設け、更にこの中間層の上に実施例
5と同様な保護層を4μm塗工した。Example 8 In Example 4, a 0.3 μm thick intermediate layer having the composition shown below was provided on the charge generation layer, and a 4 μm thick protective layer similar to Example 5 was further coated on this intermediate layer.
テトラヒドロフラン 40重量部シクロ
へキサノン 50重社部以上の様な
スシレーコーティングにより作成した感光体を複写機リ
コピーFT5510にセットし、実施例2と同様な温風
吹き付は装置を塔載し、実施例2と同じ環境条件にて、
画像評価を行なった(感光体温度は60℃)。Tetrahydrofuran: 40 parts by weight Cyclohexanone: 50 parts by weight A photoreceptor prepared by Sushiray coating was set in a copying machine, Ricopy FT5510, and hot air blowing similar to that in Example 2 was carried out by mounting the apparatus on the tower. Under the same environmental conditions as Example 2,
Image evaluation was performed (photoreceptor temperature was 60° C.).
4ooo鞍時の画像サンプルを評価した結果、実施例8
の画像はボケ、地汚れのない鮮明な画像が得られたが、
施さない場合には低温湿時に地汚れ、高湿時のボケが発
生した。As a result of evaluating the image sample when 4ooo saddled, Example 8
A clear image with no blur or background stains was obtained, but
When not applied, background staining occurred at low temperatures and humidity, and blurring occurred at high humidity.
本発明方法は前記構成からなるので次のような顕著な作
用効果を奏する。Since the method of the present invention has the above-mentioned configuration, it has the following remarkable effects.
(1)保護層を設けた場合に特に問題となる高温湿の画
像ボケ、画像ウスを防止する事ができる。(1) Image blurring and image distortion caused by high temperature and humidity, which are particularly problematic when a protective layer is provided, can be prevented.
(2)低温時の感光体の納置及び低温湿時の画像地汚れ
を防止できる。(2) It is possible to prevent the storage of the photoreceptor at low temperatures and the background smearing of images at low temperatures and humidity.
(3)有機系感光体においては、感光体のくり返し使用
後の帯電特性の劣化を防ぐことが出来る。(3) In organic photoreceptors, deterioration of charging characteristics after repeated use of the photoreceptor can be prevented.
すなわち、複写機、プリンター等の画像濃度低下2画像
濃度ムラ、カブリ、あるいは反転現像時においては地肌
汚れのない良好な画像を得る事が出来る。That is, it is possible to obtain a good image without background stains during image density reduction, image density unevenness, fog, or reverse development in copying machines, printers, etc.
第1図、第2図a、第2図す、第3図、第4図、第5図
、第6図a、第6項す及び第7図は本発明で用いる電子
写真感光体の模式断面図である。
第8図及び第10図は電子写真プロセスにおける感光体
温度と表面電位の関係を表わすグラフであり、第9図及
び第11図は電子写真プロセスにおける感光体温度、表
面電位及びコピー枚数の相関関係を表わすグラフである
。
11・・・導電性支持体
12・・・保護層
13・・・中間層
14・・・感光層
15・・・下引1台
21・・・電荷発生層
22・・・電荷輸送層
特許出願人 株式会社 リ コ −第1図
第2図(0) 第2図(b)
第3図
第4図 第5図
第7図
第8図
感光体5&友(’C)
第9図
コピー&数(枚)
第1O図
/@孔#−渫厳(’C)
第1I図
コピー枚数(旅)Figures 1, 2a, 2s, 3, 4, 5, 6a, 6s and 7 are schematic diagrams of the electrophotographic photoreceptor used in the present invention. FIG. Figures 8 and 10 are graphs showing the relationship between photoreceptor temperature and surface potential in the electrophotographic process, and Figures 9 and 11 are graphs showing the correlation between photoreceptor temperature, surface potential, and number of copies in the electrophotography process. This is a graph representing 11... Conductive support 12... Protective layer 13... Intermediate layer 14... Photosensitive layer 15... 1 undercoat 21... Charge generation layer 22... Charge transport layer Patent application People Rico Co., Ltd. - Figure 1 Figure 2 (0) Figure 2 (b) Figure 3 Figure 4 Figure 5 Figure 7 Figure 8 Photoconductor 5 & friend ('C) Figure 9 Copy & number (sheets) Figure 1O/@hole #-Yuyan ('C) Number of copies of Figure 1I (travel)
Claims (3)
電子写真感光体を帯電、露光し静電潜像を形成する工程
を含む電子写真プロセスにおいて、該感光体を常に50
℃以上に保持することを特徴とする電子写真プロセス。(1) In an electrophotographic process that includes a step of charging and exposing an electrophotographic photoreceptor comprising at least a photosensitive layer on a conductive support to form an electrostatic latent image, the photoreceptor is always
An electrophotographic process characterized by being held at temperatures above ℃.
のである特許請求の範囲第1項記載の電子写真プロセス
。(2) The electrophotographic process according to claim 1, wherein the electrophotographic photoreceptor has a protective layer provided on the photosensitive layer.
れる特許請求の範囲第1項又は第2項記載の電子写真プ
ロセス。(3) The electrophotographic process according to claim 1 or 2, wherein the photosensitive layer is formed from a charge generating material and a charge transporting material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1830988A JPH01191883A (en) | 1988-01-27 | 1988-01-27 | Electrophotographic process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1830988A JPH01191883A (en) | 1988-01-27 | 1988-01-27 | Electrophotographic process |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01191883A true JPH01191883A (en) | 1989-08-01 |
Family
ID=11968014
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1830988A Pending JPH01191883A (en) | 1988-01-27 | 1988-01-27 | Electrophotographic process |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01191883A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7979003B2 (en) | 2007-09-28 | 2011-07-12 | Fuji Xerox Co., Ltd. | Image forming apparatus and image forming method |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6095467A (en) * | 1983-07-06 | 1985-05-28 | Fuji Photo Film Co Ltd | Preventing method of deterioration of electrophotographic sensitive body |
JPS62296180A (en) * | 1986-06-17 | 1987-12-23 | Canon Inc | Electrophotographic method |
-
1988
- 1988-01-27 JP JP1830988A patent/JPH01191883A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6095467A (en) * | 1983-07-06 | 1985-05-28 | Fuji Photo Film Co Ltd | Preventing method of deterioration of electrophotographic sensitive body |
JPS62296180A (en) * | 1986-06-17 | 1987-12-23 | Canon Inc | Electrophotographic method |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7979003B2 (en) | 2007-09-28 | 2011-07-12 | Fuji Xerox Co., Ltd. | Image forming apparatus and image forming method |
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