JPH04171457A - Electrophotographic sensitized body, and copying machine and facsimile using the same sensitized body - Google Patents
Electrophotographic sensitized body, and copying machine and facsimile using the same sensitized bodyInfo
- Publication number
- JPH04171457A JPH04171457A JP2298063A JP29806390A JPH04171457A JP H04171457 A JPH04171457 A JP H04171457A JP 2298063 A JP2298063 A JP 2298063A JP 29806390 A JP29806390 A JP 29806390A JP H04171457 A JPH04171457 A JP H04171457A
- Authority
- JP
- Japan
- Prior art keywords
- intermediate layer
- electrophotographic
- electrophotographic photoreceptor
- layer
- substituted
- 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
- 239000000463 material Substances 0.000 claims abstract description 14
- 229920000642 polymer Polymers 0.000 claims abstract description 10
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 7
- 229920001577 copolymer Polymers 0.000 claims abstract description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 5
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 4
- 125000003118 aryl group Chemical group 0.000 claims abstract description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 4
- 108091008695 photoreceptors Proteins 0.000 claims description 57
- 239000000126 substance Substances 0.000 claims description 12
- 238000004140 cleaning Methods 0.000 claims description 7
- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 109
- 229920005989 resin Polymers 0.000 description 34
- 239000011347 resin Substances 0.000 description 34
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 239000000843 powder Substances 0.000 description 12
- 230000007547 defect Effects 0.000 description 10
- 239000003973 paint Substances 0.000 description 10
- 239000000049 pigment Substances 0.000 description 10
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 8
- 229910052782 aluminium Inorganic materials 0.000 description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 8
- -1 maleic anhydride ester Chemical class 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 239000006185 dispersion Substances 0.000 description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 239000004576 sand Substances 0.000 description 6
- 239000004677 Nylon Substances 0.000 description 5
- 230000004888 barrier function Effects 0.000 description 5
- 239000011324 bead Substances 0.000 description 5
- 238000003618 dip coating Methods 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 229920001778 nylon Polymers 0.000 description 5
- 229920002037 poly(vinyl butyral) polymer Polymers 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
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 5
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- 229910000410 antimony oxide Inorganic materials 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 4
- 239000005011 phenolic resin Substances 0.000 description 4
- 229920006122 polyamide resin Polymers 0.000 description 4
- 229920001225 polyester resin Polymers 0.000 description 4
- 239000004645 polyester resin Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 229920001187 thermosetting polymer Polymers 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 229910003437 indium oxide Inorganic materials 0.000 description 3
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000012046 mixed solvent Substances 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 239000002985 plastic film Substances 0.000 description 3
- 229920006255 plastic film Polymers 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 2
- 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 2
- 239000001856 Ethyl cellulose Substances 0.000 description 2
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- 229920002396 Polyurea Polymers 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-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
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000004917 carbon fiber Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 229920001249 ethyl cellulose Polymers 0.000 description 2
- 235000019325 ethyl cellulose Nutrition 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 229940097275 indigo Drugs 0.000 description 2
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 229920000767 polyaniline Polymers 0.000 description 2
- 229920005668 polycarbonate resin Polymers 0.000 description 2
- 239000004431 polycarbonate resin Substances 0.000 description 2
- 239000005518 polymer electrolyte Substances 0.000 description 2
- 229920000128 polypyrrole Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
- 238000001226 reprecipitation Methods 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-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
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- YFPSDOXLHBDCOR-UHFFFAOYSA-N Pyrene-1,6-dione Chemical compound C1=CC(C(=O)C=C2)=C3C2=CC=C2C(=O)C=CC1=C32 YFPSDOXLHBDCOR-UHFFFAOYSA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 206010064127 Solar lentigo Diseases 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 description 1
- 230000004397 blinking Effects 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- JBTHDAVBDKKSRW-UHFFFAOYSA-N chembl1552233 Chemical compound CC1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 JBTHDAVBDKKSRW-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 150000002085 enols Chemical class 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- HDERJYVLTPVNRI-UHFFFAOYSA-N ethene;ethenyl acetate Chemical group C=C.CC(=O)OC=C HDERJYVLTPVNRI-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 238000012690 ionic polymerization Methods 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
- 229920002382 photo conductive polymer Polymers 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- DNXIASIHZYFFRO-UHFFFAOYSA-N pyrazoline Chemical compound C1CN=NC1 DNXIASIHZYFFRO-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229940073450 sudan red Drugs 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Landscapes
- Fax Reproducing Arrangements (AREA)
- Photoreceptors In Electrophotography (AREA)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は電子写真感光体に関し、詳しくは導電性支持体
と感光層との間に設けられた中間層の改良に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to an electrophotographic photoreceptor, and more particularly to an improvement in an intermediate layer provided between a conductive support and a photosensitive layer.
[従来の技術]
一般に、カールソンタイプの電子写真感光体においては
、帯電−露光を繰り返したときに一定の画像濃度でカブ
リの見られない画像を形成する上で、暗部電位と明部電
位の安定性が重要になっている。[Prior Art] In general, in a Carlson type electrophotographic photoreceptor, stabilization of dark area potential and bright area potential is required to form an image with a constant image density and no fog when charging and exposure are repeated. Gender has become important.
この実現の為に、支持体から感光層への電荷注入性改良
、支持体と感光層との接着性改良、感光層の塗工性向上
、支持体上の欠陥の被覆などの機能を有する中間層を支
持体と感光層との間に設けることが提案されている。To achieve this, an intermediate layer with functions such as improving charge injection from the support to the photosensitive layer, improving adhesion between the support and the photosensitive layer, improving coatability of the photosensitive layer, and covering defects on the support is developed. It has been proposed to provide a layer between the support and the photosensitive layer.
また、感光層を電荷発生層と電荷輸送層に機能分離した
積層構造を有するものが提案されているが、一般に電荷
発生層は極めて薄い層として、例えば0.5μm程度で
設けられているため、支持体表面の欠陥、汚れ、付着物
または傷などが電荷、発生層の膜厚を不均一とする原因
となる。電荷発生層の膜厚が不均一であると感光体に感
度ムラを生じるので、電荷発生層をできるだけ均一なも
のとすることが要求されている。In addition, a layered structure in which the photosensitive layer is functionally separated into a charge generation layer and a charge transport layer has been proposed, but the charge generation layer is generally provided as an extremely thin layer, for example, about 0.5 μm. Defects, dirt, deposits, scratches, etc. on the surface of the support cause the thickness of the charge generation layer to be non-uniform. If the thickness of the charge generation layer is non-uniform, uneven sensitivity will occur in the photoreceptor, so it is required that the charge generation layer be made as uniform as possible.
このようなことから電荷発生層と支持体との間にバリヤ
ー層としての機能、接着層としての機能および支持体上
の欠陥を被覆する機能を有する中間層を設けることが提
案されている。For this reason, it has been proposed to provide an intermediate layer between the charge generating layer and the support, which functions as a barrier layer, an adhesive layer, and covers defects on the support.
これまで感光層と支持体との間に設ける層として、ポリ
アミド(特開昭46−47344号、特開昭52−25
638号、特開昭58−95351号)、ポリエステル
(特開昭52−20836号、特開昭54−26738
号)、ボリウレクン(特開昭49−10044号、特開
昭53−89435号)、カゼイン(特開昭55−10
3556号)、ポリペプチド(特開昭53−48523
号)、ポリビニルアルコール(特開昭52−10024
0号)、ポリビニルピロリドン(特開昭48−3093
6号)、酢酸ビニル−エチレン共重合体(特開昭48−
26141号)、無水マレイン酸エステル重合体(特開
昭52−10138号)、ポリビニルブチラール(特開
昭57−90639号、特開昭58−106549号)
、第四級アンモニウム塩含有重合体(特開昭51−12
6149号、特開昭56−60448号)、エチルセル
ロース(特開昭55−143564号)などを用いるこ
とが知られている。Until now, polyamide (JP-A-46-47344, JP-A-52-25) has been used as a layer between the photosensitive layer and the support.
638, JP-A-58-95351), polyester (JP-A-52-20836, JP-A-54-26738)
No.), Boriurekun (Japanese Patent Application Laid-Open No. 10044-1982, No. 89435-1989), Casein (Japanese Patent Application Laid-Open No. 10-1989)
No. 3556), polypeptide (Japanese Unexamined Patent Publication No. 53-48523)
No.), polyvinyl alcohol (JP-A-52-10024
No. 0), polyvinylpyrrolidone (Japanese Patent Application Laid-open No. 48-3093
No. 6), vinyl acetate-ethylene copolymer (Japanese Patent Application Laid-open No. 1973-
26141), maleic anhydride ester polymer (JP 52-10138), polyvinyl butyral (JP 57-90639, JP 58-106549)
, quaternary ammonium salt-containing polymer (JP-A-51-12
6149, JP-A-56-60448), ethyl cellulose (JP-A-55-143564), and the like are known to be used.
[発明が解決しようとする課題]
しかしながら、前述の材料を中間層として用いた電子写
真感光体では、温湿度変化により中間層の抵抗が変化す
るために、低温低湿下から高温高湿下の全環境に対して
常に安定した電位特性、画質を得るのが困難であった。[Problems to be Solved by the Invention] However, in an electrophotographic photoreceptor using the above-mentioned material as an intermediate layer, the resistance of the intermediate layer changes due to changes in temperature and humidity. It was difficult to always obtain stable potential characteristics and image quality with respect to the environment.
例えば、中間層の電気抵抗が高くなる低温低湿下では感
光体を繰り返し使用した場合、中間層に電荷が残留する
ため明部電位、残留電位が上昇しコピーした画像にカブ
リを生じたり、反転現象を行なう電子写真方式のブリン
ク−にこのような感光体を用いた場合には画像の濃度が
薄くなったり、一定の画質を有するコピーが得られない
問題があった。For example, if a photoconductor is used repeatedly under low temperature and low humidity conditions where the electrical resistance of the intermediate layer increases, charges remain in the intermediate layer, resulting in an increase in the bright area potential and residual potential, causing fog in the copied image or reversal phenomenon. When such a photoreceptor is used for blinking in an electrophotographic method, there are problems in that the density of the image becomes low and copies with a certain image quality cannot be obtained.
また、高温高湿下になると中間層の低抵抗化によりバリ
ヤー機能が低下し、支持体側からのキャリアー注入が増
え暗部電位が低下してしまう。Furthermore, under high temperature and high humidity conditions, the barrier function decreases due to the lower resistance of the intermediate layer, and carrier injection from the support side increases, resulting in a decrease in dark area potential.
このため、高温高温下ではコピーした画像の濃度が薄く
なったり、反転現象を行なう電子写真方式のプリンター
にこのような感光体を用いた場合には、画像に黒点状の
欠陥(黒ポチ)、およびカブリを生じ易(なるといった
問題があった。For this reason, the density of copied images becomes lighter under high temperatures, and when such a photoreceptor is used in an electrophotographic printer that performs a reversal phenomenon, black dot-like defects (black spots) may appear on the image. There were also problems such as easy fogging.
したがって本発明の目的は低温低湿下から高温高湿下に
至る全環境に対して安定した電位特性と画像の得られる
電子写真感光体を提供することにある。Therefore, an object of the present invention is to provide an electrophotographic photoreceptor that can provide stable potential characteristics and images in all environments ranging from low temperature and low humidity to high temperature and high humidity.
また、本発明の別の目的は支持体上の欠陥を十分に被覆
できる中間層を形成して、欠陥のない良好な画像を形成
し得る電子写真感光体を提供することにある。Another object of the present invention is to provide an electrophotographic photoreceptor that can form an intermediate layer that can sufficiently cover defects on a support, thereby forming good images without defects.
[課題を解決するための手段]
すなわち、本発明の電子写真感光体は導電性支持体上に
、中間層を介して感光層を設けた電子写真感光体におい
て、該中間層が下記一般式[1]で示される単位成分を
有する重合体または共重合体を含有することを特徴とす
るものである。[Means for Solving the Problems] That is, the electrophotographic photoreceptor of the present invention is an electrophotographic photoreceptor in which a photosensitive layer is provided on a conductive support via an intermediate layer, and the intermediate layer has the following general formula [ It is characterized by containing a polymer or copolymer having the unit component shown in [1].
+cH2−C+
(式中R゛は水素原子又は低級アルキル基、R2は置換
又は非置換アルキル基、置換又は非置換アルケニル基、
置換又は非置換芳香族環、置換又は非置換複素環、置換
又は非置換シクロアルキル基を示す)。+cH2-C+ (wherein R' is a hydrogen atom or a lower alkyl group, R2 is a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group,
substituted or unsubstituted aromatic ring, substituted or unsubstituted heterocycle, substituted or unsubstituted cycloalkyl group).
第1表に実際に本発明に用いられる樹脂の例を示す。Table 1 shows examples of resins actually used in the present invention.
第1表
本発明の電子写真感光体は前述の樹脂を中間層に含有す
ることにより、低温低湿下における残留電位の上昇およ
び高温高温下におけるバリヤー機能の低下による暗部電
位の低下などの環境変動を防止することができる。Table 1 The electrophotographic photoreceptor of the present invention contains the above-mentioned resin in the intermediate layer to prevent environmental changes such as an increase in residual potential at low temperatures and low humidity and a decrease in dark area potential due to a decrease in barrier function at high temperatures. It can be prevented.
本発明における中間層用の樹脂は各環境下において体積
抵抗の変動をあまり起こさず、この樹脂を中間層とした
場合に、環境変動による特性変動の少ない電子写真感光
体を得ることができる。これに対して、通常の中間層に
用いられる樹脂は常温常温下より高温高湿下に移行する
と、抵抗が3ケタはど低くなったりするが、本発明に用
いられる中間層用の樹脂は余り変化を示さない。The resin for the intermediate layer in the present invention does not cause much variation in volume resistivity under various environments, and when this resin is used as the intermediate layer, it is possible to obtain an electrophotographic photoreceptor with little variation in characteristics due to environmental changes. On the other hand, the resistance of ordinary resins used for the intermediate layer decreases by as low as three digits when moving from normal temperature to high temperature and high humidity, but the resin for the intermediate layer used in the present invention has a low resistance. Shows no change.
本発明の電子写真感光体を構成する中間層の作成に用い
られる樹脂は一般式[1]で示される単位成分に相当す
るモノマーを適当な溶媒に溶かし、これにアゾビスイソ
ブチロニトリル(AIBN)、過酸化ベンゾイル等のラ
ジカル開始剤又は金属ナトリウムの様なイオン重合開始
剤を投入して反応を行なわせることによって製造し得る
。The resin used to create the intermediate layer constituting the electrophotographic photoreceptor of the present invention is prepared by dissolving a monomer corresponding to the unit component represented by the general formula [1] in an appropriate solvent, and adding azobisisobutyronitrile (AIBN) to the monomer corresponding to the unit component represented by the general formula [1]. ), it can be produced by adding a radical initiator such as benzoyl peroxide or an ionic polymerization initiator such as sodium metal to carry out the reaction.
また、製造後の樹脂中には、開始剤残分等の不純物が残
っている場合が多いので、その使用前に再沈殿、洗浄な
どの精製工程を加えることが好ましい。Further, since impurities such as initiator residues often remain in the resin after production, it is preferable to add purification steps such as reprecipitation and washing before use.
次に、本発明に用いられるグラフト化ポリアミド樹脂と
して前記樹脂例[]]の具体的製造例を示す。Next, a specific production example of the resin example []] as the grafted polyamide resin used in the present invention will be shown.
〈製造例〉
メタクリル酸メチルとアセトンとをナトリウムメチラー
トの存在下で縮合して得られた下記化合物60g、
H3
H2−c
」
AIBNo、8gをメタノール100g中に溶解し、7
0℃で12時間加熱撹拌し、重合反応を行なった。<Production Example> 60 g of the following compound obtained by condensing methyl methacrylate and acetone in the presence of sodium methylate, 8 g of H3 H2-c'' AIB No. was dissolved in 100 g of methanol, and 7
The mixture was heated and stirred at 0° C. for 12 hours to carry out a polymerization reaction.
次に、室温まで冷却した反応混合物にアセトン250g
加えたのち、脱塩水中で再沈殿精製を行なった。その後
、真空乾燥を行なったところ28gの樹脂(1)を得た
。Next, 250 g of acetone was added to the reaction mixture cooled to room temperature.
After addition, reprecipitation purification was performed in demineralized water. Thereafter, vacuum drying was performed to obtain 28 g of resin (1).
本発明の中間層は前述の樹脂(下記構造式)%式%
1 一般式[1〕
(式中R1は水素原子又は低級アルキル基、好ましくは
水素原子又はメチル基であり、R2は置換又は非置換ア
ルキル基、置換又は非置換アルケニル基、置換又は非置
換芳香族環、置換又は非置換複素環、置換又は非置換シ
クロアルキル基を示す)のみで構成されていても、必要
に応じて他の脂、添加剤、導電性物質等を加えた系で構
成されていでもよい。The intermediate layer of the present invention has the above-mentioned resin (the following structural formula)% formula% 1 general formula [1] (wherein R1 is a hydrogen atom or a lower alkyl group, preferably a hydrogen atom or a methyl group, and R2 is a substituted or unsubstituted Substituted alkyl group, substituted or unsubstituted alkenyl group, substituted or unsubstituted aromatic ring, substituted or unsubstituted heterocycle, substituted or unsubstituted cycloalkyl group), if necessary, other It may be composed of a system to which fat, additives, conductive substances, etc. are added.
ここで、加える他の樹脂の例としては、共重合ナイロン
、N−アルコキシメチル化ナイロンなどのポリアミド樹
脂、ポリエステル樹脂、ポリウレタン樹脂、ポリウレア
樹脂、フェノール樹脂などが挙げられる。Here, examples of other resins to be added include polyamide resins such as copolymerized nylon and N-alkoxymethylated nylon, polyester resins, polyurethane resins, polyurea resins, and phenol resins.
添加剤の例としては、酸化チタン、アルミナ、樹脂など
の粉体類、界面活性剤、シリコーンレベリング剤、シラ
ンカップリング剤、チタネートカップリング剤などが挙
げられる。Examples of additives include powders such as titanium oxide, alumina, and resins, surfactants, silicone leveling agents, silane coupling agents, and titanate coupling agents.
導電性物質を用いる場合、アルミニウム、銅、ニッケル
、銀などの金属粉体、鱗片状金属粉体および、金属短繊
維:酸化アンチモン、酸化インジウム、酸化スズなどの
導電性金属酸化物;ポリピロール、ポリアニリン、高分
子電解質などの高分子導電材;カーボンファイバー、カ
ーボンブラック、グラファイト粉体またはこれらの導電
性物質で表面を被覆した導電性粉体などが挙げられる。When using conductive substances, metal powders such as aluminum, copper, nickel, and silver, scaly metal powders, short metal fibers: conductive metal oxides such as antimony oxide, indium oxide, and tin oxide; polypyrrole, polyaniline, etc. , polymeric conductive materials such as polymer electrolytes; carbon fiber, carbon black, graphite powder, or conductive powder whose surface is coated with these conductive substances.
本発明の中間層の厚さは電子写真特性および支持体上の
欠陥を考慮して設定されるものであり、0.1〜50μ
m程度まで設定し得るが、通常は05〜5μm、導電性
物質を添加したときは1〜30μmが好適である。The thickness of the intermediate layer of the present invention is set in consideration of electrophotographic characteristics and defects on the support, and is 0.1 to 50 μm.
The thickness can be set up to about m, but it is usually 05 to 5 μm, and preferably 1 to 30 μm when a conductive substance is added.
中間層の塗工は浸漬コーティング、スプレーコーティン
グ、ロールコーティングなどの方法で行なうことができ
る。The intermediate layer can be applied by dip coating, spray coating, roll coating, or the like.
また、本発明ではバリヤー性のコントロールなどの必要
に応じて、中間層上に樹脂を主°成分とする第二の中間
層を設けることができる。Further, in the present invention, a second intermediate layer containing a resin as a main component can be provided on the intermediate layer as necessary for controlling barrier properties.
第二の中間層に用いられる樹脂材料としては、ポリアミ
ド樹脂、ポリエステル樹脂、ポリウレタン樹脂、ポリウ
レア樹脂、フェノール樹脂などが挙げられる。Examples of the resin material used for the second intermediate layer include polyamide resin, polyester resin, polyurethane resin, polyurea resin, and phenol resin.
第二の中間層の厚さは0.1〜5μmが好適であり、前
述の中間層と同様の方法により塗工され得る。The thickness of the second intermediate layer is preferably 0.1 to 5 μm, and can be coated by the same method as the above-mentioned intermediate layer.
本発明においては、感光層は単一層型でも、電荷発生層
と電荷輸送層とに機能分め〃した積層構造型でも良い。In the present invention, the photosensitive layer may be of a single layer type or a laminated structure type in which functions are divided into a charge generation layer and a charge transport layer.
積層構造型感光体の電荷発生層はスーダンレッド、グイ
アンプル−などのアゾ顔料、ピレンキノン、アントアン
トロンなどのキノン顔料、キノシアニン顔料、ベニレン
顔料、インジゴ、チオインジゴなどのインジゴ顔料、ア
ズレニウム塩顔料、銅フタロシアニン、チタニルオキソ
フタロシアニンなどのフタロシアニン顔料などの電荷発
生物質をポリビニルブチラール、ポリスチレン、ポリ酢
酸ビニル、アクリル樹脂、ポリビニルピロリドン、エチ
ルセルロース、酢酸酪酸セルロースなどの結着剤樹脂を
含有する溶液に分散させ、この分散液を前述の中間層の
上に塗工することによって作成できる。The charge generation layer of the laminated photoreceptor contains azo pigments such as Sudan red and Guianpuru, quinone pigments such as pyrenequinone and anthinthrone, quinocyanine pigments, benylene pigments, indigo pigments such as indigo and thioindigo, azlenium salt pigments, copper phthalocyanine, A charge generating material such as a phthalocyanine pigment such as titanyl oxophthalocyanine is dispersed in a solution containing a binder resin such as polyvinyl butyral, polystyrene, polyvinyl acetate, acrylic resin, polyvinyl pyrrolidone, ethyl cellulose, cellulose acetate butyrate, and this dispersion can be created by coating on the aforementioned intermediate layer.
このような、電荷発生層の膜厚は5μm以下、好ましく
は0.05〜2μmである。The thickness of such a charge generation layer is 5 μm or less, preferably 0.05 to 2 μm.
電荷発生層の上に設ける電荷輸送層は主鎖または側鎖に
ビフェニレン、アントラセン、ピレン、フェナントレン
などの構造を有する多環芳香族化合物、インドール、カ
ルバゾール、オキサジアゾール、ピラゾリンなどの含窒
素環式化合物、ヒドラゾン化合物、スチリル化合物など
の電荷輸送性物質を成膜性を有する樹脂に溶解させた塗
工液を用いて形成される。The charge transport layer provided on the charge generation layer is a polycyclic aromatic compound having a structure such as biphenylene, anthracene, pyrene, or phenanthrene in the main chain or side chain, or a nitrogen-containing cyclic compound such as indole, carbazole, oxadiazole, or pyrazoline. It is formed using a coating liquid in which a charge transporting substance such as a compound, a hydrazone compound, or a styryl compound is dissolved in a resin having film-forming properties.
このようにして作成する理由は電荷輸送性物質が一般に
低分子量で、それ自身では成膜性に乏しい点を補うこと
にある。The reason for preparing the film in this manner is to compensate for the fact that charge transporting substances generally have a low molecular weight and are poor in film forming properties by themselves.
このような成膜性を有する樹脂としては、ポリエステル
樹脂、ポリカーボネート樹脂、ポリメタクリル酸エステ
ル樹脂、ポリスチレン樹脂などが挙げられる。Examples of resins having such film-forming properties include polyester resins, polycarbonate resins, polymethacrylate resins, and polystyrene resins.
電荷輸送層の厚さは5〜40μm、好ましくは10〜3
0μmである。The thickness of the charge transport layer is 5 to 40 μm, preferably 10 to 3 μm.
It is 0 μm.
また、本発明ではポリビニルカルバゾール、ポリビニル
アントラセンなどの有機光導電性ポリマー層;セレン蒸
着層、セレン−テルル蒸着層、アモルファスシリコン層
なども感光層に用いることができる。Further, in the present invention, an organic photoconductive polymer layer such as polyvinylcarbazole or polyvinylanthracene; a selenium vapor deposition layer, a selenium-tellurium vapor deposition layer, an amorphous silicon layer, etc. can also be used as the photosensitive layer.
本発明においては光導電層の構成として前記の層構成以
外に電荷輸送層上に電荷発生層を設けた層構成も可能で
ある。In the present invention, as the structure of the photoconductive layer, in addition to the layer structure described above, a layer structure in which a charge generation layer is provided on a charge transport layer is also possible.
一方、本発明で用いる導電性支持体は導電性を有するも
のであれば何れでもよく、例えばアルミニウム、銅、ク
ロム、ニッケル、亜鉛、耐食鋼(ステンレス)などの金
属をドラムまたはシート状に成型したもの、アルミニウ
ムや銅などの金属箔をプラスチックフィルムにラミネー
トしたもの、アルミニウム、酸化インジウム、酸化スズ
などをプラスチックフィルムに蒸着したもの、あるいは
導電性物質を単独または適当なバインダー樹脂とともに
塗布して導電層を設けたプラスチックフィルム、紙など
が挙げられる。On the other hand, the conductive support used in the present invention may be any material as long as it has conductivity, such as a drum or sheet made of metal such as aluminum, copper, chromium, nickel, zinc, or corrosion-resistant steel (stainless steel). A conductive layer can be formed by laminating a metal foil such as aluminum or copper onto a plastic film, by vapor-depositing aluminum, indium oxide, tin oxide, etc. onto a plastic film, or by coating a conductive substance alone or with a suitable binder resin. Examples include plastic films and paper provided with
この導電層に用いられる導電性物質としては、アルミニ
ウム、銅、ニッケル、銀等の金属粉体、金属箔及び金属
短繊維;酸化アンチモン、酸化インジウム、酸化スズな
どの導電性金属酸化物;ポリピロール、ポリアニリン、
高分子電解質などの高分子導電材:カーボンファイバー
、カーボンブラック、グラファイト粉体;有機および無
機の電解質;またはこれらの導電性物質で表面を被覆し
た導電性粉体などが挙げられる。The conductive substances used in this conductive layer include metal powders such as aluminum, copper, nickel, and silver, metal foils, and short metal fibers; conductive metal oxides such as antimony oxide, indium oxide, and tin oxide; polypyrrole, polyaniline,
Polymer conductive materials such as polymer electrolytes: carbon fiber, carbon black, graphite powder; organic and inorganic electrolytes; or conductive powder whose surface is coated with these conductive substances.
また、導電層に用いられるバインダー樹脂としては、ポ
リアミド樹脂、ポリエステル樹脂、アクリル樹脂、ポリ
アミノ酸エステル樹脂、ポリ酢酸ビニル樹脂、ポリカー
ボネート樹脂、ポリビニルホルマール、ポリビニルブチ
ラール、ポリビニルアルキルエーテル、ポリアルキレン
エーテル、ポリウレタンエラストマーなどの熱可塑性樹
脂、熱硬化性ポリウレタン、フェノール樹脂、熱硬化性
エポキシ樹脂などの熱硬化性樹脂が挙げられる。Binder resins used in the conductive layer include polyamide resin, polyester resin, acrylic resin, polyamino acid ester resin, polyvinyl acetate resin, polycarbonate resin, polyvinyl formal, polyvinyl butyral, polyvinyl alkyl ether, polyalkylene ether, and polyurethane elastomer. Examples include thermosetting resins such as thermoplastic resins such as thermosetting resins, thermosetting polyurethanes, phenolic resins, and thermosetting epoxy resins.
導電性物質とバインダー樹脂の混合比は5:1〜1:5
程度である。この混合比は導電層の電気抵抗値、表面性
、塗布適性などを考慮して決められる。The mixing ratio of conductive material and binder resin is 5:1 to 1:5
That's about it. This mixing ratio is determined in consideration of the electrical resistance value, surface properties, coating suitability, etc. of the conductive layer.
導電性物質が粉体の場合にはボールミル、ロールミル、
サンドミルなどを用いて常法により混合物を調製して用
いる。If the conductive substance is a powder, use a ball mill, roll mill,
A mixture is prepared and used in a conventional manner using a sand mill or the like.
また、他の添加剤として界面活性剤、シランカップリン
グ剤、チタネートカップリング剤、シリコーンオイル、
シリコーンレベリング剤などを添加してもよい。In addition, other additives include surfactants, silane coupling agents, titanate coupling agents, silicone oil,
A silicone leveling agent or the like may also be added.
本発明の電子写真感光体は電子写真複写機に使用するの
みならず、レーザービームプリンター、CRTプリンタ
ー、LEDプリンター、液晶プリンター、レーザー製版
及びファクシミリ用のプリンター等の電子写真応用分野
にも広く用いることができる。The electrophotographic photoreceptor of the present invention can be used not only in electrophotographic copying machines, but also in a wide range of electrophotographic applications such as laser beam printers, CRT printers, LED printers, liquid crystal printers, laser plate making, and facsimile printers. I can do it.
第1図に本発明の電子写真感光体を装着したドラム型感
光体を用いた一般的な転写式電子写真装置の概略構成を
示す。FIG. 1 shows a schematic configuration of a general transfer type electrophotographic apparatus using a drum type photoreceptor equipped with the electrophotographic photoreceptor of the present invention.
第1図において、11は像担持部材としてのドラム型感
光体であり、軸11aを中心に矢印方向に所定の周速度
で回転駆動される。該感光体11はその回転過程で、帯
電手段12によって、その周面に正又は負の所定電位の
均一帯電を受け、次いで露光部13において、不図示の
像露光手段により、光像露光しくスリット露光、レーザ
ービーム走査露光等)を受ける。これにより、感光体周
面に露光像に対応した静電潜像が順次形成される。In FIG. 1, reference numeral 11 denotes a drum-type photoreceptor as an image bearing member, which is rotated at a predetermined circumferential speed in the direction of the arrow around a shaft 11a. During the rotation process, the photoreceptor 11 is uniformly charged to a predetermined positive or negative potential on its circumferential surface by the charging means 12, and then in the exposure section 13, it is exposed to a slit by an image exposure means (not shown). exposure, laser beam scanning exposure, etc.). As a result, electrostatic latent images corresponding to the exposed images are sequentially formed on the circumferential surface of the photoreceptor.
その静電潜像は次いで現像手段14でトナー現像され、
そのトナー現像像が転写手段15により、不図示の給紙
部から感光体11と転写手段15との開に感光体11の
回転と同期取りされて給送された転写材Pの面に順次転
写される。The electrostatic latent image is then developed with toner by the developing means 14,
The toner developed image is sequentially transferred by the transfer means 15 onto the surface of the transfer material P fed from a paper feeding section (not shown) in synchronization with the rotation of the photoreceptor 11 between the photoreceptor 11 and the transfer means 15. be done.
像転写を受けた転写材Pは感光体面から分離されて像定
着手段18へ導入されて像定着を受け、複写物(コピー
)として機外ヘプリントアウトされる。The transfer material P that has undergone the image transfer is separated from the photoreceptor surface, introduced into the image fixing means 18, where the image is fixed, and is printed out outside the machine as a copy.
像転写後の感光体11の表面はクリーニング手段16に
よって転写残りトナーの除去を受けて清浄面化されて繰
り返して像形成に使用される。After the image has been transferred, the surface of the photoreceptor 11 is cleaned by a cleaning means 16 to remove residual toner and is repeatedly used for image formation.
感光体11の均一帯電手段12としてはコロナ帯電装置
が一般に広く使用されている。また、転写装置15とし
ても、コロナ転写手段が広(一般に使用されている。電
子写真装置として、上述の感光体11、現像手段14及
びクリーニング手段16等の構成要素のうち、複数のも
のを装置ユニットとして一体に結合して構成し、このユ
ニットを装置本体に対して着脱自在に構成しても良い。As the uniform charging means 12 for the photoreceptor 11, a corona charging device is generally widely used. In addition, as the transfer device 15, a corona transfer device is widely used (generally used). They may be constructed by being combined together as a unit, and this unit may be configured to be detachably attached to the main body of the apparatus.
例えば、感光体41とクリーニング手段16とを一体化
して草−の装置ユニットとし、装置本体のレール等の案
内手段を用いて着脱自在の構成にしても良い。この際に
、上記の装置ユニットの方に帯電手段12及び/又は現
像手段14を伴って構成しても良い。For example, the photoreceptor 41 and the cleaning means 16 may be integrated into a single device unit, which can be attached and detached using guide means such as rails on the main body of the device. At this time, the above-mentioned device unit may be configured to include the charging means 12 and/or the developing means 14.
また、光像露光しは電子写真装置を複写機又はプリンタ
ーとして使用する場合には、原稿からの反射光、透過光
又は原稿を読み取り信号化し、この信号によってレーザ
ービームの走査、発光ダイオードアレイの駆動又は液晶
シャッターアレイの駆動等によって行なわれる。In addition, when an electrophotographic device that exposes a light image is used as a copying machine or a printer, the reflected light from the original, the transmitted light, or the original is read and converted into a signal, and this signal is used to scan the laser beam and drive the light emitting diode array. Alternatively, this may be performed by driving a liquid crystal shutter array or the like.
また、ファクシミリのプリンターとして使用する場合に
は、光像露光しは受信データをプリントする為の露光に
なる。第2図はこの場合の1例をブロック図で示したも
のである。Furthermore, when used as a facsimile printer, the optical image exposure is exposure for printing received data. FIG. 2 is a block diagram showing an example of this case.
第2図において、コントローラ21は画像読み取り部2
0とプリンター29を制御する。コントローラ21の全
体はCPU27によって制御されている。画像読み取り
部からの読み取りデータは送信回路23を通して相手局
に送信される。In FIG. 2, the controller 21 is the image reading section 2.
0 and printer 29. The entire controller 21 is controlled by a CPU 27. The read data from the image reading section is transmitted to the other party's station through the transmitting circuit 23.
相手局から受けたデータは受信回路22を通してプリン
ター29に送られる。画像メモリ26には、所定の画像
データが記憶される。プリンタコントローラ28はプリ
ンター29を制御している。24は電話である。Data received from the partner station is sent to the printer 29 through the receiving circuit 22. Image memory 26 stores predetermined image data. A printer controller 28 controls a printer 29. 24 is a telephone.
回線25から受信された画像(回線を介して接続された
リモート端末からの画像情報)は受信回路22で復調さ
れた後に、CPU27で画像情報の復号処理が行なわれ
て順次画像メモリ26に格納される。そして、少な(と
も1頁分の画像が画像メモリ26に格納されると、その
頁の画像記録を行なう。CPU27は画像メモリ26か
ら1頁分の画像情報を読み出してプリンターコントロー
ラ28に復号化された1頁分の画像情報を送出する。プ
リンターコントローラ28はCPTJ27からの1頁分
の画像情報を受は取ると、その頁の画像情報記録を行な
うべく、プリンター29を制御する。なお、CPU27
はプリンター29による記録中に次の頁分の受信を行な
っている。Images received from the line 25 (image information from a remote terminal connected via the line) are demodulated by the receiving circuit 22, and then decoded by the CPU 27 and sequentially stored in the image memory 26. Ru. Then, when one page worth of image information is stored in the image memory 26, the image information for that page is recorded. When the printer controller 28 receives the image information for one page from the CPTJ 27, it controls the printer 29 to record the image information for that page.
The next page is being received while the printer 29 is recording.
以上の様に、本発明の像保持部材を装着した電子写真装
置をプリンターとして、画像の受信と記録とが行なわれ
得る。As described above, an electrophotographic apparatus equipped with the image holding member of the present invention can be used as a printer to receive and record images.
以下に、具体的実施例を挙げて本発明をさらに詳しく説
明する。The present invention will be explained in more detail below by giving specific examples.
実施例1
導電性酸化チタン粉体(酸化アンチモン10%含有酸化
スズで被覆)50部、フェノール樹脂25部、メチルセ
ロソルブ20部、メタノール5部およびシリコーンオイ
ル(ポリジメチルシロキサン−ポリオキシアルキレン共
重合体、平均分子量3000)0.002部を直径1m
mのガラスピーズを収容したサンドミル装置で2時間混
合分散して導電層用塗料を調製した。Example 1 50 parts of conductive titanium oxide powder (coated with tin oxide containing 10% antimony oxide), 25 parts of phenolic resin, 20 parts of methyl cellosolve, 5 parts of methanol, and silicone oil (polydimethylsiloxane-polyoxyalkylene copolymer) , average molecular weight 3000) 0.002 parts in diameter 1 m
A conductive layer coating material was prepared by mixing and dispersing the mixture for 2 hours in a sand mill device containing m glass beads.
アルミニウムシリンダー(外径30mmX長さ260m
m)上に上記塗料を浸漬塗布し、140℃で30分間乾
燥させて、膜厚20μmの導電層を形成させた。Aluminum cylinder (outer diameter 30mm x length 260m)
m) The above paint was applied by dip coating and dried at 140° C. for 30 minutes to form a conductive layer with a thickness of 20 μm.
次に、第1表に例示の重合体(1)5部をメタノール9
5部に溶解し、中間層作成用塗料を調製した。Next, 5 parts of the polymer (1) shown in Table 1 was added to 9 parts of methanol.
The mixture was dissolved in 5 parts to prepare a paint for forming an intermediate layer.
この塗料を上記導電層上に浸漬塗布し、100℃で20
分間乾燥させて、膜厚0.5μmの中間層を形成させた
。This paint was dip-coated on the conductive layer and heated at 100°C for 20 minutes.
It was dried for a minute to form an intermediate layer with a thickness of 0.5 μm.
次に下記構造式のジスアゾ顔料3部、
ポリビニルベンザール(ベンザール化率70%、重量平
均分子量13000)2部およびシクロへキサノン35
部を直径1mmのガラスピーズを収容したサンドミル装
置で12時間混合分散した後に、メチルエチルケトン(
MEK)60部を加えて電荷発生層形成用分散液を調製
した。この分散液を上記それぞれの中間層上に浸漬塗布
し、80℃で20分間乾燥させ、膜厚0.15μmの電
荷発生層を形成させた。Next, 3 parts of a disazo pigment with the following structural formula, 2 parts of polyvinylbenzal (benzalization rate 70%, weight average molecular weight 13000), and 35 parts of cyclohexanone.
After mixing and dispersing for 12 hours in a sand mill device containing glass beads with a diameter of 1 mm, methyl ethyl ketone (
A dispersion liquid for forming a charge generation layer was prepared by adding 60 parts of MEK. This dispersion was dip-coated onto each of the above intermediate layers and dried at 80° C. for 20 minutes to form a charge generation layer with a thickness of 0.15 μm.
次に、下記構造式のスチリル化合物10部及びポリカー
ボネート(重量平均分子量46000)10部をジクロ
ルメタン20部、モノクロルベンゼン40部の混合溶媒
中に溶解し、この溶液を上記の電荷発生層上に浸漬塗布
して120″Cで60分間乾燥させ、膜厚18μmの電
荷輸送層を形成させた。Next, 10 parts of a styryl compound having the following structural formula and 10 parts of polycarbonate (weight average molecular weight 46,000) were dissolved in a mixed solvent of 20 parts of dichloromethane and 40 parts of monochlorobenzene, and this solution was dip-coated onto the above charge generation layer. This was dried at 120''C for 60 minutes to form a charge transport layer with a thickness of 18 μm.
このようにして製造した電子写真感光体を反転現像方式
のレーザープリンター(帯電−露光一現像一転写一クリ
ーニングのプロセスを1.5秒サイクルで繰り返す)に
取り付け、常温常温下(23℃、50%RH)および高
温高湿下(30℃、85%RH)の環境で電子写真特性
の評価を行なった。The electrophotographic photoreceptor thus manufactured was attached to a reversal development type laser printer (the process of charging-exposure-development-transfer-cleaning is repeated in a 1.5-second cycle) at room temperature (23°C, 50% The electrophotographic properties were evaluated in a high temperature and high humidity environment (30° C., 85% RH).
この結果、第2表に示すように実施例1の感光体では、
暗部電位(v n)と明部電位(■L)との差が太き(
、十分な電位コントラストが得られたと共に、高温高温
下でも暗部電位(V D)が安定し、黒点上の欠陥(黒
ポチ)、カブリの認められない良好な画像が得られた。As a result, as shown in Table 2, in the photoreceptor of Example 1,
The difference between the dark potential (v n) and the bright potential (■L) is large (
In addition to obtaining sufficient potential contrast, the dark area potential (VD) was stable even under high temperature conditions, and good images with no defects on black spots (black spots) or fog were obtained.
実施例2〜5
中間層形成用塗料として、第1表に例示の重合体(2)
、(4)、(6)又は(8)をそれぞれ用いた外には、
実施例1と同様にして電子写真感光体を製造し、それぞ
れ実施例2〜5とした。Examples 2 to 5 Polymer (2) exemplified in Table 1 as a paint for forming an intermediate layer
, (4), (6) or (8), respectively.
Electrophotographic photoreceptors were manufactured in the same manner as in Example 1, and named as Examples 2 to 5, respectively.
これらの各感光体を実施例1と同様にして評価したとこ
ろ、いずれも高温高温下でも暗部電位(V、)が安定し
、黒点上の欠陥(黒ポチ)、カブリの認められない良好
な画像を形成し得たこの結果を第2表に示す。When each of these photoreceptors was evaluated in the same manner as in Example 1, the dark potential (V, ) was stable even under high temperature conditions, and good images were obtained with no defects on sunspots (black spots) or fog. The results are shown in Table 2.
比較例1
中間層形成用塗料として、第1表に例示の樹脂(1)の
代わりに、N−メトキシメチル化6ナイロン(重量平均
分子量150000、メトキシメチル基置換率28%)
を用いた外には、実施例1と同様にして電子写真感光体
を製造した。Comparative Example 1 As a paint for forming an intermediate layer, N-methoxymethylated 6-nylon (weight average molecular weight 150,000, methoxymethyl group substitution rate 28%) was used instead of resin (1) illustrated in Table 1.
An electrophotographic photoreceptor was manufactured in the same manner as in Example 1 except that the following was used.
この感光体を実施例1と同様にして評価したところ、高
温高湿下になると帯電能が悪化し、暗部電位(V o)
の低下が見られ、画像上には黒点上の欠陥(黒ポチ)が
発生するようになった。When this photoreceptor was evaluated in the same manner as in Example 1, the charging ability deteriorated under high temperature and high humidity conditions, and the dark area potential (V o )
A decrease in image quality was observed, and defects on black spots (black spots) began to appear on the image.
この結果を第2表に示す。The results are shown in Table 2.
実施例6
第1表に例示の樹脂(3)5部をメタノール95部に溶
解し、中間層形成用塗料を調製した。Example 6 A paint for forming an intermediate layer was prepared by dissolving 5 parts of the resin (3) shown in Table 1 in 95 parts of methanol.
この塗料をアルミニウムシリンダー(外径30mmx長
さ360μmm)上に浸漬塗布し、100°Cで20分
間乾燥させて、膜厚1.0μmの中間層を形成させた。This paint was dip-coated onto an aluminum cylinder (outer diameter 30 mm x length 360 μm) and dried at 100° C. for 20 minutes to form an intermediate layer with a thickness of 1.0 μm.
次に、下記構造式のて型チクニルフタロシアニン顔料4
部、
ポリビニルブチラール(ブチラール化率68%、重量平
均分子量24000)2部およびシクロへキサノン34
部を直径1mmのガラスピーズを収容したサンドミル装
置で100時間混分散した後、テトラヒドロフラン(T
HF)60部を加えて電荷発生層形成用分散液を調製し
た。この分散液を上記それぞれの中間層上に浸漬塗布し
、80℃で20分間乾燥させ、膜厚0.2μmの電荷発
生層を形成した。Next, a type chichnylphthalocyanine pigment 4 with the following structural formula
1 part, 2 parts of polyvinyl butyral (butyralization rate 68%, weight average molecular weight 24,000) and 34 parts of cyclohexanone
After mixing and dispersing for 100 hours in a sand mill device containing glass beads with a diameter of 1 mm, tetrahydrofuran (T
A dispersion liquid for forming a charge generation layer was prepared by adding 60 parts of HF). This dispersion was dip coated onto each of the above intermediate layers and dried at 80° C. for 20 minutes to form a charge generation layer with a thickness of 0.2 μm.
次に、実施例1で用いたスチリル化合物10部およびポ
リカーボネート (重量平均分子量63000)10部
をジクロルメタン15部、モノクロルベンゼン45部の
混合溶媒中に溶解し、この溶液を上記の電荷発生層上に
浸漬塗布し、120℃で60分間乾燥させて、膜厚25
μmの電荷輸送層を形成させた。Next, 10 parts of the styryl compound used in Example 1 and 10 parts of polycarbonate (weight average molecular weight 63,000) were dissolved in a mixed solvent of 15 parts of dichloromethane and 45 parts of monochlorobenzene, and this solution was applied onto the above charge generation layer. Dip coating and drying at 120°C for 60 minutes to achieve a film thickness of 25
A charge transport layer of μm was formed.
このようにして製造した電子写真感光体を複写機(帯電
−露光−現像−転写−クニーニングのプロセスを1.0
秒サイクルで繰り返す)に装着した。The electrophotographic photoreceptor produced in this manner was transferred to a copying machine (charging-exposure-development-transfer-cleaning process to 1.0
(repeated in second cycles).
この感光体に対して低温低湿下(15°C115%RH
)の環境で電子写真特性の評価を行なったところ、表2
に示すようにこの感光体では、暗部電位(V D)と明
部電位(VL)との差が大きく、十分な電位コントラス
トが得られた。更に、連続1000枚の画像を出したと
ころ、明部電位(V L)の上昇も少なく安定した画像
が得られた。This photoconductor was tested under low temperature and low humidity (15°C, 115%RH).
), the electrophotographic characteristics were evaluated in the environment shown in Table 2.
As shown in FIG. 2, in this photoreceptor, the difference between the dark area potential (VD) and the light area potential (VL) was large, and sufficient potential contrast was obtained. Furthermore, when 1000 images were continuously produced, stable images were obtained with little increase in bright area potential (VL).
実施例7〜10
中間層形成用塗料として、第1表に例示の重合体樹脂(
9)、(5)、(7)又は(11)をそれぞれ用いた外
には、実施例6と同様にして電子写真感光体を製造して
、それぞれ実施例7〜10とした。Examples 7 to 10 As a paint for forming an intermediate layer, polymer resins (
Electrophotographic photoreceptors were manufactured in the same manner as in Example 6 except that 9), (5), (7), or (11) were used, respectively, to give Examples 7 to 10, respectively.
これらの各感光体を実施例6と同様にして評価したとこ
ろ、いずれの感光体でも暗部電位 (V O)と暗部電
位(VL)との差が大きく、十分な電位コントラストが
得られると共に、連続1000枚の画像を出しても、明
部電位(VL)の上昇が少なく、安定した画像を形成し
得た
この結果を第3表に示す。When each of these photoreceptors was evaluated in the same manner as in Example 6, the difference between the dark area potential (V O) and the dark area potential (VL) was large for each photoreceptor, and sufficient potential contrast was obtained, as well as continuous Even after printing 1000 images, stable images were formed with little increase in bright area potential (VL). The results are shown in Table 3.
比較例2
中間層形成用塗料として第1表に例示の樹脂(3)の代
わりに、アルコール可溶性共重合ナイロン(重量平均分
子量81000)を用いたほかには、実施例6と同様に
して電子写真感光体を製造して、比較例2とした。Comparative Example 2 Electrophotography was carried out in the same manner as in Example 6, except that alcohol-soluble copolymerized nylon (weight average molecular weight 81,000) was used instead of resin (3) shown in Table 1 as the paint for forming the intermediate layer. A photoreceptor was manufactured as Comparative Example 2.
この感光体を実施例6と同様にして評価したところ、連
続1000枚の繰り返しで明部電位(VL)が上昇して
、画像上にカブリを生じるようになった。When this photoreceptor was evaluated in the same manner as in Example 6, it was found that the bright area potential (VL) increased after 1000 continuous sheets were printed, causing fog on the image.
この結果を表2に示す。The results are shown in Table 2.
実施例11
導電性酸化チタン粉体(10%酸化アンチモンを含有す
る酸化スズで被覆)30部、ルチルギ酸化チクン粉体2
0部、第1表に例示の重合体[10]を20部、メタノ
ール20部、2−プロパツール10部を直径1mmのガ
ラスピーズを収容したサンドミル装置で1時間混合分散
して導電層用塗料を調製した。Example 11 30 parts of conductive titanium oxide powder (coated with tin oxide containing 10% antimony oxide), 2 parts of rutile formate powder
0 parts, 20 parts of the polymer [10] illustrated in Table 1, 20 parts of methanol, and 10 parts of 2-propertool were mixed and dispersed for 1 hour in a sand mill containing glass beads with a diameter of 1 mm to prepare a coating material for a conductive layer. was prepared.
アルミニウムシリンダー(外径60 m m X長さ2
60mm)上に上記塗料を浸漬塗布し、160℃で30
分間乾燥させ、膜厚16μmの中間層を形成させた。Aluminum cylinder (outer diameter 60 mm x length 2
60mm), apply the above paint by dip coating and heat it at 160℃ for 30 minutes.
It was dried for minutes to form an intermediate layer with a thickness of 16 μm.
次に、アルコール可溶性共重合ナイロン(重量平均分子
量75000)5部をメタノール95部に溶解し、上記
中間層上に浸漬塗布後、80℃で10分間乾燥させ、膜
厚0.3μmの第二の中間層を形成させた。Next, 5 parts of alcohol-soluble copolymerized nylon (weight average molecular weight 75,000) was dissolved in 95 parts of methanol, and after coating on the above intermediate layer by dip coating, it was dried at 80°C for 10 minutes to form a second layer with a film thickness of 0.3 μm. An intermediate layer was formed.
次に下記構造式のジスアゾ顔料2部、
ポリビニルブチラール(ブチラール化率72%、重量平
均分子量18000)1部およびシクロへキサノン30
部を直径1mmのガラスピーズを収容したサンドミル装
置で244時間混分散した後に、メチルエチルケトン(
MEK)65部を加えて電荷発生層形成用分散液を調製
した。この分散液を第二の中間層上に浸漬塗布し、80
℃で20分間乾燥させて、膜厚0.25μmの電荷発生
層を形成させた。Next, 2 parts of a disazo pigment with the following structural formula, 1 part of polyvinyl butyral (butyral conversion rate 72%, weight average molecular weight 18,000) and 30 parts of cyclohexanone.
After mixing and dispersing for 244 hours in a sand mill device containing glass beads with a diameter of 1 mm, methyl ethyl ketone (
A dispersion liquid for forming a charge generation layer was prepared by adding 65 parts of MEK. This dispersion was dip coated onto the second intermediate layer and
It was dried at .degree. C. for 20 minutes to form a charge generation layer with a thickness of 0.25 .mu.m.
次に、下記構造式のヒドラゾン化合物11部及ポリカー
ボネート(重量平均分子量46000)12部をジクロ
ルメタン20部、モノクロルベンゼン40部の混合溶媒
中に溶解し、この溶液を上記の電荷発生層上に浸漬塗布
し、120℃で60分間乾燥させて、膜厚204zmの
電荷輸送層を形成させた。Next, 11 parts of a hydrazone compound of the following structural formula and 12 parts of polycarbonate (weight average molecular weight 46,000) were dissolved in a mixed solvent of 20 parts of dichloromethane and 40 parts of monochlorobenzene, and this solution was dip-coated onto the above charge generation layer. Then, it was dried at 120° C. for 60 minutes to form a charge transport layer with a thickness of 204 zm.
このようにして製造した電子写真感光体を複写機(帯電
−露光−現像−転写−クリーニングのプロセスを0.8
秒サイクルで繰り返す)に装着した。The electrophotographic photoreceptor produced in this manner was transferred to a copying machine (charging-exposure-development-transfer-cleaning process of 0.8
(repeated in second cycles).
この感光体に対して低温低湿下(15℃、lO%RH)
の環境で電子写真特性の評価を行なったところ、表3に
示すようにこの感光体では暗部電位 (V o)と明部
電位 (V L)の差が太き(、十分な電位コントラス
トが得られた。さらに、連続1000枚の画像を出した
処、明部電位 (■L)の上昇も少なく安定した画像が
得られた。For this photoreceptor, under low temperature and low humidity (15°C, 10%RH)
When the electrophotographic characteristics were evaluated in an environment of Furthermore, when 1000 images were printed in succession, stable images were obtained with little increase in bright area potential (L).
結果を第4表に示す。The results are shown in Table 4.
実施例12
第二の中間層を設けなかった外には実施例11と同様に
して中間層、電荷発生層及び電荷輸送層を形成させ、実
施例12の電子写真感光体を製造した。Example 12 An electrophotographic photoreceptor of Example 12 was manufactured by forming an intermediate layer, a charge generation layer, and a charge transport layer in the same manner as in Example 11 except that the second intermediate layer was not provided.
この感光体を実施例11と同様にして評価したところ、
暗部電位(V O)と明部電位(V L)との差が大き
く、十分な電位コントラストが得られると共に連続10
00枚の画像を出しても、明部電位(V L)の上昇が
少な(、安定した画像が得られた。この結果を第4表に
示す。When this photoreceptor was evaluated in the same manner as in Example 11,
The difference between the dark area potential (V O) and the light area potential (V L) is large, sufficient potential contrast is obtained, and continuous 10
Even when 00 images were produced, stable images were obtained with little increase in bright area potential (VL). The results are shown in Table 4.
比較例3及び4
導電性酸化チタン粉体およびルチル型酸化チタン粉体を
含む中間層用塗料樹脂として、)エノール樹脂を用いた
外には、実施例11および12と同様にして電子写真感
光体を製造し、それぞれ比較例3及び4とした。Comparative Examples 3 and 4 An electrophotographic photoreceptor was prepared in the same manner as in Examples 11 and 12, except that an enol resin was used as the coating resin for the intermediate layer containing conductive titanium oxide powder and rutile-type titanium oxide powder. were produced and designated as Comparative Examples 3 and 4, respectively.
これらの各感光体を実施例11と同様にして評価したと
ころ、比較例3では連続1000枚の繰り返しで明部電
位(V L)が上昇し、画像上にはカブリを生じるよう
になった。また、中間層上に直接に電荷発生層、電荷輸
送層を設けた比゛較例4では、中間層のバリヤー性が不
足して、支持体側からの電荷注入が大きく、暗部電位(
■Il+)が低いため、画像形成に必要な電位コントラ
ストが得られなかった。この結果を表3に示す。When each of these photoreceptors was evaluated in the same manner as in Example 11, it was found that in Comparative Example 3, the bright area potential (VL) increased after 1000 continuous sheets were printed, and fog appeared on the image. In addition, in Comparative Example 4 in which a charge generation layer and a charge transport layer were provided directly on the intermediate layer, the barrier properties of the intermediate layer were insufficient, the charge injection from the support side was large, and the dark potential (
(2) Due to the low Il+), the potential contrast necessary for image formation could not be obtained. The results are shown in Table 3.
第2表
第3表
第4表
[発明の効果]
本発明の電子写真感光体は導電性支持体と感光層との間
の中間層形成用樹脂中に、前記の重合体又は共重合体樹
脂を含有させることにより、低温低湿下から高温高温下
に至る全環境において安定した電位特性を示すと共に良
好な画像を形成させることができる。Table 2 Table 3 Table 4 [Effects of the Invention] The electrophotographic photoreceptor of the present invention contains the above polymer or copolymer resin in the resin for forming an intermediate layer between the conductive support and the photosensitive layer. By containing , stable potential characteristics can be exhibited in all environments ranging from low temperature and low humidity to high temperature and high temperature, and a good image can be formed.
第1図は本発明の電子写真感光体を装着した転写式複写
機の模式的断面図、第2図は本発明の電。
子写真感光体をプリンターとしたファクシミリシステム
のブロック図である。
[図中の主な符号]
]l・・・ドラム型感光体
12・・・帯電手段
13・・・露光部
14・・・現像手段
15・・・転写手段
16・・・クリーニング手段
18・・・像定着手段
L・・・光像露光
P・・・転写材
代理人 弁理士 山 下 穣 平FIG. 1 is a schematic sectional view of a transfer type copying machine equipped with the electrophotographic photoreceptor of the present invention, and FIG. FIG. 2 is a block diagram of a facsimile system in which a secondary photographic photoreceptor is used as a printer. [Main symbols in the figure] l...Drum type photoreceptor 12...Charging means 13...Exposure section 14...Developing means 15...Transfer means 16...Cleaning means 18...・Image fixing means L...Light image exposure P...Transfer material agent Patent attorney Johei Yamashita
Claims (1)
電子写真感光体において、該中間層が下記一般式[1]
で示される単位成分を有する重合体又は共重合体を主材
として含有することを特徴とする電子写真感光体: ▲数式、化学式、表等があります▼一般式[1] (式中R^1は水素原子又は低級アルキル基、R^2は
置換又は非置換アルキル基、置換又は非置換アルケニル
基、置換又は非置換芳香族環、置換又は非置換複素環、
置換又は非置換シクロアルキル基を示す)。 (2)中間層が導電性物質を含有することを特徴とする
請求項1に記載の電子写真感光体。 (3)電子写真感光体、潜像形成手段、形成された潜像
を現像する手段及び現像された像を転写材に転写する手
段を有する電子写真装置において、該電子写真感光体が
請求項1に記載のものであることを特徴とする電子写真
装置。 (5)請求項1に記載の電子写真感光体並びに帯電手段
、現像手段及びクリーニング手段の少なくとも1つを一
体に支持してユニットを形成し、装置本体に着脱自在の
単一ユニットとしたことを特徴とする装置ユニット。 (6)請求項1に記載の電子写真感光体、潜像形成手段
、形成した潜像を現像する手段及び現像した像を転写材
に転写する手段を有することを特徴とする電子写真装置
。 (7)請求項1に記載の電子写真感光体、潜像形成手段
及び現像した像を転写材に転写する手段を備えた電子写
真装置並びにリモート端末からなる画像情報を受信する
受信手段を有することを特徴とするファクシミリ。[Scope of Claims] (1) In an electrophotographic photoreceptor having a photosensitive layer on a conductive support via an intermediate layer, the intermediate layer has the following general formula [1]
An electrophotographic photoreceptor characterized by containing as a main material a polymer or copolymer having a unit component represented by: ▲There are mathematical formulas, chemical formulas, tables, etc.▼General formula [1] is a hydrogen atom or a lower alkyl group, R^2 is a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aromatic ring, a substituted or unsubstituted heterocycle,
(represents a substituted or unsubstituted cycloalkyl group). (2) The electrophotographic photoreceptor according to claim 1, wherein the intermediate layer contains a conductive substance. (3) An electrophotographic apparatus comprising an electrophotographic photoreceptor, a latent image forming means, a means for developing the formed latent image, and a means for transferring the developed image to a transfer material, wherein the electrophotographic photoreceptor is the one according to claim 1. An electrophotographic device characterized by being as described in . (5) The electrophotographic photoreceptor according to claim 1 and at least one of the charging means, the developing means, and the cleaning means are integrally supported to form a unit, and the single unit is detachably attached to the main body of the apparatus. Characteristic equipment unit. (6) An electrophotographic apparatus comprising the electrophotographic photoreceptor according to claim 1, a latent image forming means, a means for developing the formed latent image, and a means for transferring the developed image onto a transfer material. (7) The electrophotographic photoreceptor according to claim 1, an electrophotographic apparatus comprising a latent image forming means and a means for transferring a developed image to a transfer material, and a receiving means for receiving image information from a remote terminal. A facsimile machine featuring
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2298063A JPH04171457A (en) | 1990-11-02 | 1990-11-02 | Electrophotographic sensitized body, and copying machine and facsimile using the same sensitized body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2298063A JPH04171457A (en) | 1990-11-02 | 1990-11-02 | Electrophotographic sensitized body, and copying machine and facsimile using the same sensitized body |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04171457A true JPH04171457A (en) | 1992-06-18 |
Family
ID=17854657
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2298063A Pending JPH04171457A (en) | 1990-11-02 | 1990-11-02 | Electrophotographic sensitized body, and copying machine and facsimile using the same sensitized body |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04171457A (en) |
-
1990
- 1990-11-02 JP JP2298063A patent/JPH04171457A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPH0540360A (en) | Electrophotographic sensitive body | |
JPH06208238A (en) | Electrophotographic receptor and electrophotographic device using the same | |
JPH0345961A (en) | Electrophotographic sensitive body | |
EP0497523B1 (en) | Image-holding member, and electrophotographic apparatus, apparatus unit, and facsimile machine employing the same | |
JPH04353860A (en) | Photosensitive material for electrophotography, electrophotographic device and facsimille equiped with this photosensitive material for electrophotography | |
EP0421888B1 (en) | Electrophotographic sensitive medium and apparatus using the same | |
JPH04170552A (en) | Electrophotosensitive material and copying machine and facsimile using this material | |
JP3226110B2 (en) | Electrophotographic photoreceptor | |
JP2801427B2 (en) | Electrophotographic photoreceptor, electrophotographic apparatus and facsimile using the same | |
JP2692962B2 (en) | Electrophotographic photoreceptor | |
JPH04171457A (en) | Electrophotographic sensitized body, and copying machine and facsimile using the same sensitized body | |
JPH0619176A (en) | Electrophotographic sensitive body, and electrophotographic apparatus and facsimile provided with the same | |
JP3050673B2 (en) | Electrophotographic photoreceptor and electrophotographic apparatus having the same | |
JP3192018B2 (en) | Electrophotographic photoreceptor and electrophotographic apparatus having the same | |
JP3697038B2 (en) | Electrophotographic photoreceptor, process cartridge and electrophotographic apparatus having the electrophotographic photoreceptor | |
JPH04170550A (en) | Electrophotosensitive material and copying machine and facsimile using this material | |
JPH08179542A (en) | Electrophotographic photoreceptor and process cartridge having same and electrophotographic apparatus | |
JP2839112B2 (en) | Electrophotographic photosensitive member, copying machine and facsimile using the same | |
JP3684043B2 (en) | Electrophotographic photoreceptor, process cartridge and electrophotographic apparatus having the electrophotographic photoreceptor | |
JP3287595B2 (en) | Electrophotographic photoreceptor, electrophotographic apparatus using the same, apparatus unit and facsimile | |
JPH04350664A (en) | Electrophotographic sensitive body, electrophotographic device and facsimile having this electrophotographic sensitive body | |
JP2700009B2 (en) | Electrophotographic photoreceptor | |
JP2637563B2 (en) | Electrophotographic photoreceptor | |
JPH04171458A (en) | Electrophotographic sensitized body, and copying machine and facsimile using the same sensitized body | |
JP3101469B2 (en) | Electrophotographic photoreceptor, electrophotographic apparatus and apparatus unit having the electrophotographic photoreceptor |