JP2009288786A - リン酸アミン含有電荷発生層光導電体 - Google Patents
リン酸アミン含有電荷発生層光導電体 Download PDFInfo
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- JP2009288786A JP2009288786A JP2009124956A JP2009124956A JP2009288786A JP 2009288786 A JP2009288786 A JP 2009288786A JP 2009124956 A JP2009124956 A JP 2009124956A JP 2009124956 A JP2009124956 A JP 2009124956A JP 2009288786 A JP2009288786 A JP 2009288786A
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- Prior art keywords
- phosphate
- bis
- layer
- charge
- diamine
- 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.)
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- -1 Amine phosphate Chemical class 0.000 title claims abstract description 55
- 229910019142 PO4 Inorganic materials 0.000 title claims abstract description 44
- 239000010452 phosphate Substances 0.000 title claims abstract description 42
- 239000000758 substrate Substances 0.000 claims abstract description 36
- 229910052757 nitrogen Inorganic materials 0.000 claims description 50
- 239000000203 mixture Substances 0.000 claims description 36
- SJHHDDDGXWOYOE-UHFFFAOYSA-N oxytitamium phthalocyanine Chemical compound [Ti+2]=O.C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 SJHHDDDGXWOYOE-UHFFFAOYSA-N 0.000 claims description 26
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 24
- 239000000049 pigment Substances 0.000 claims description 21
- 239000002253 acid Substances 0.000 claims description 16
- 230000002378 acidificating effect Effects 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 15
- ATHGHQPFGPMSJY-UHFFFAOYSA-N spermidine Chemical compound NCCCCNCCCN ATHGHQPFGPMSJY-UHFFFAOYSA-N 0.000 claims description 14
- PFNFFQXMRSDOHW-UHFFFAOYSA-N spermine Chemical compound NCCCNCCCCNCCCN PFNFFQXMRSDOHW-UHFFFAOYSA-N 0.000 claims description 14
- 239000000126 substance Substances 0.000 claims description 13
- NHFDKKSSQWCEES-UHFFFAOYSA-N dihydrogen phosphate;tris(2-hydroxyethyl)azanium Chemical group OP(O)(O)=O.OCCN(CCO)CCO NHFDKKSSQWCEES-UHFFFAOYSA-N 0.000 claims description 9
- 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 claims description 9
- NSTLSXSJOBWQLC-UHFFFAOYSA-N 1-aminopropan-2-ol;phosphoric acid Chemical compound CC(O)CN.OP(O)(O)=O NSTLSXSJOBWQLC-UHFFFAOYSA-N 0.000 claims description 7
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 claims description 7
- 229940063673 spermidine Drugs 0.000 claims description 7
- 229940063675 spermine Drugs 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- DCAYPVUWAIABOU-UHFFFAOYSA-N alpha-n-hexadecene Natural products CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- UNXNGGMLCSMSLH-UHFFFAOYSA-N dihydrogen phosphate;triethylazanium Chemical compound OP(O)(O)=O.CCN(CC)CC UNXNGGMLCSMSLH-UHFFFAOYSA-N 0.000 claims description 6
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 claims description 6
- 229960001340 histamine Drugs 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 150000004982 aromatic amines Chemical class 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- ATBNMWWDBWBAHM-UHFFFAOYSA-N n-decyl-n-methyldecan-1-amine Chemical compound CCCCCCCCCCN(C)CCCCCCCCCC ATBNMWWDBWBAHM-UHFFFAOYSA-N 0.000 claims description 5
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 claims description 4
- QVINBVLRRUFUKK-UHFFFAOYSA-N 4-butyl-n-[4-[4-[4-(4-butyl-n-(4-propan-2-ylphenyl)anilino)phenyl]phenyl]phenyl]-n-(4-propan-2-ylphenyl)aniline Chemical compound C1=CC(CCCC)=CC=C1N(C=1C=CC(=CC=1)C=1C=CC(=CC=1)C=1C=CC(=CC=1)N(C=1C=CC(CCCC)=CC=1)C=1C=CC(=CC=1)C(C)C)C1=CC=C(C(C)C)C=C1 QVINBVLRRUFUKK-UHFFFAOYSA-N 0.000 claims description 3
- ZUVCYFMOHFTGDM-UHFFFAOYSA-N hexadecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCOP(O)(O)=O ZUVCYFMOHFTGDM-UHFFFAOYSA-N 0.000 claims description 3
- PRMHOXAMWFXGCO-UHFFFAOYSA-M molport-000-691-708 Chemical compound N1=C(C2=CC=CC=C2C2=NC=3C4=CC=CC=C4C(=N4)N=3)N2[Ga](Cl)N2C4=C(C=CC=C3)C3=C2N=C2C3=CC=CC=C3C1=N2 PRMHOXAMWFXGCO-UHFFFAOYSA-M 0.000 claims description 3
- PUMLPTZCSBHSGK-UHFFFAOYSA-N n-[4-[4-[4-(4-butyl-n-(2-methylphenyl)anilino)phenyl]phenyl]phenyl]-n-(4-butylphenyl)-2-methylaniline Chemical compound C1=CC(CCCC)=CC=C1N(C=1C(=CC=CC=1)C)C1=CC=C(C=2C=CC(=CC=2)C=2C=CC(=CC=2)N(C=2C=CC(CCCC)=CC=2)C=2C(=CC=CC=2)C)C=C1 PUMLPTZCSBHSGK-UHFFFAOYSA-N 0.000 claims description 3
- GVFRJEQSPPYVMT-UHFFFAOYSA-N n-[4-[4-[4-(4-butyl-n-(3-methylphenyl)anilino)phenyl]phenyl]phenyl]-n-(4-butylphenyl)-3-methylaniline Chemical compound C1=CC(CCCC)=CC=C1N(C=1C=C(C)C=CC=1)C1=CC=C(C=2C=CC(=CC=2)C=2C=CC(=CC=2)N(C=2C=CC(CCCC)=CC=2)C=2C=C(C)C=CC=2)C=C1 GVFRJEQSPPYVMT-UHFFFAOYSA-N 0.000 claims description 3
- BFNYZDOLJUQOGT-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCC)N.P(=O)(OCCCCCCCCCCCCCCCC)(O)O Chemical compound C(CCCCCCCCCCCCCCCCC)N.P(=O)(OCCCCCCCCCCCCCCCC)(O)O BFNYZDOLJUQOGT-UHFFFAOYSA-N 0.000 claims description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
- FNSUFQUHOSSRJL-UHFFFAOYSA-N n-[4-[4-[4-(4-butyl-n-(2,5-dimethylphenyl)anilino)phenyl]phenyl]phenyl]-n-(4-butylphenyl)-2,5-dimethylaniline Chemical compound C1=CC(CCCC)=CC=C1N(C=1C(=CC=C(C)C=1)C)C1=CC=C(C=2C=CC(=CC=2)C=2C=CC(=CC=2)N(C=2C=CC(CCCC)=CC=2)C=2C(=CC=C(C)C=2)C)C=C1 FNSUFQUHOSSRJL-UHFFFAOYSA-N 0.000 claims description 2
- AFHTYONPPKJCIT-UHFFFAOYSA-N 4-[4-[4-(3-chloroanilino)phenyl]phenyl]-n-(3-chlorophenyl)-2,3-diphenylaniline Chemical compound ClC1=CC=CC(NC=2C=CC(=CC=2)C=2C=CC(=CC=2)C=2C(=C(C=3C=CC=CC=3)C(NC=3C=C(Cl)C=CC=3)=CC=2)C=2C=CC=CC=2)=C1 AFHTYONPPKJCIT-UHFFFAOYSA-N 0.000 claims 1
- 238000003384 imaging method Methods 0.000 abstract description 32
- 108091008695 photoreceptors Proteins 0.000 abstract description 4
- 230000002950 deficient Effects 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 164
- 235000021317 phosphate Nutrition 0.000 description 33
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 27
- 230000000903 blocking effect Effects 0.000 description 27
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 21
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- 238000000576 coating method Methods 0.000 description 21
- 239000012790 adhesive layer Substances 0.000 description 18
- 239000011248 coating agent Substances 0.000 description 17
- 239000000523 sample Substances 0.000 description 17
- 238000000034 method Methods 0.000 description 13
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 13
- 229920000515 polycarbonate Polymers 0.000 description 12
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 11
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 11
- 150000001412 amines Chemical class 0.000 description 10
- 239000011230 binding agent Substances 0.000 description 10
- 239000004417 polycarbonate Substances 0.000 description 9
- 239000005011 phenolic resin Substances 0.000 description 8
- 229920001568 phenolic resin Polymers 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 239000002019 doping agent Substances 0.000 description 7
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- 239000007787 solid Substances 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 6
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 229920002635 polyurethane Polymers 0.000 description 6
- 239000004814 polyurethane Substances 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 5
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- 238000006243 chemical reaction Methods 0.000 description 5
- 229910044991 metal oxide Inorganic materials 0.000 description 5
- 150000004706 metal oxides Chemical class 0.000 description 5
- 150000002989 phenols Chemical class 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- 239000002861 polymer material Substances 0.000 description 5
- 238000000634 powder X-ray diffraction Methods 0.000 description 5
- NAJNIFLHKZVKRU-UHFFFAOYSA-N 2-methyl-n-[4-[4-(2-methylanilino)phenyl]phenyl]aniline Chemical compound CC1=CC=CC=C1NC1=CC=C(C=2C=CC(NC=3C(=CC=CC=3)C)=CC=2)C=C1 NAJNIFLHKZVKRU-UHFFFAOYSA-N 0.000 description 4
- 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
- 239000004952 Polyamide Substances 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 4
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- 150000003014 phosphoric acid esters Chemical class 0.000 description 4
- 229920002647 polyamide Polymers 0.000 description 4
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- JTPNRXUCIXHOKM-UHFFFAOYSA-N 1-chloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1 JTPNRXUCIXHOKM-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 3
- PDGBJJIOGJPBLC-UHFFFAOYSA-N 3-chloro-n-[4-[4-[4-(n-(3-chlorophenyl)anilino)phenyl]phenyl]phenyl]-n-phenylaniline Chemical compound ClC1=CC=CC(N(C=2C=CC=CC=2)C=2C=CC(=CC=2)C=2C=CC(=CC=2)C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=C(Cl)C=CC=2)=C1 PDGBJJIOGJPBLC-UHFFFAOYSA-N 0.000 description 3
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 3
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- HCNHNBLSNVSJTJ-UHFFFAOYSA-N 1,1-Bis(4-hydroxyphenyl)ethane Chemical compound C=1C=C(O)C=CC=1C(C)C1=CC=C(O)C=C1 HCNHNBLSNVSJTJ-UHFFFAOYSA-N 0.000 description 2
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- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/05—Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
- G03G5/0503—Inert supplements
- G03G5/051—Organic non-macromolecular compounds
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- G—PHYSICS
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- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/05—Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
- G03G5/0503—Inert supplements
- G03G5/051—Organic non-macromolecular compounds
- G03G5/0514—Organic non-macromolecular compounds not comprising cyclic groups
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0601—Acyclic or carbocyclic compounds
- G03G5/0612—Acyclic or carbocyclic compounds containing nitrogen
- G03G5/0614—Amines
- G03G5/06142—Amines arylamine
- G03G5/06144—Amines arylamine diamine
- G03G5/061443—Amines arylamine diamine benzidine
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0601—Acyclic or carbocyclic compounds
- G03G5/0612—Acyclic or carbocyclic compounds containing nitrogen
- G03G5/0614—Amines
- G03G5/06142—Amines arylamine
- G03G5/06144—Amines arylamine diamine
- G03G5/061446—Amines arylamine diamine terphenyl-diamine
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0664—Dyes
- G03G5/0696—Phthalocyanines
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/001—Electric or magnetic imagery, e.g., xerography, electrography, magnetography, etc. Process, composition, or product
- Y10S430/103—Radiation sensitive composition or product containing specified antioxidant
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Photoreceptors In Electrophotography (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/129,969 US7968263B2 (en) | 2008-05-30 | 2008-05-30 | Amine phosphate containing photogenerating layer photoconductors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009288786A true JP2009288786A (ja) | 2009-12-10 |
| JP2009288786A5 JP2009288786A5 (cg-RX-API-DMAC7.html) | 2012-07-12 |
Family
ID=41020857
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009124956A Withdrawn JP2009288786A (ja) | 2008-05-30 | 2009-05-25 | リン酸アミン含有電荷発生層光導電体 |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US7968263B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2128708B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2009288786A (cg-RX-API-DMAC7.html) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7985521B2 (en) * | 2008-05-30 | 2011-07-26 | Xerox Corporation | Anthracene containing photoconductors |
| US7968261B2 (en) * | 2008-05-30 | 2011-06-28 | Xerox Corporation | Zirconocene containing photoconductors |
| US8048601B2 (en) * | 2008-05-30 | 2011-11-01 | Xerox Corporation | Aminosilane and self crosslinking acrylic resin hole blocking layer photoconductors |
| US8012656B2 (en) * | 2008-05-30 | 2011-09-06 | Xerox Corporation | Backing layer containing photoconductor |
| US8003289B2 (en) * | 2008-05-30 | 2011-08-23 | Xerox Corporation | Ferrocene containing photoconductors |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1020506A (en) | 1960-12-29 | 1966-02-16 | Gevaert Photo Prod Nv | Photoconductive recording materials |
| US3245786A (en) * | 1964-06-08 | 1966-04-12 | Gevaert Photo Prod Nv | Photoconductive recording materials |
| US4265990A (en) * | 1977-05-04 | 1981-05-05 | Xerox Corporation | Imaging system with a diamine charge transport material in a polycarbonate resin |
| US4298697A (en) | 1979-10-23 | 1981-11-03 | Diamond Shamrock Corporation | Method of making sheet or shaped cation exchange membrane |
| US4338390A (en) | 1980-12-04 | 1982-07-06 | Xerox Corporation | Quarternary ammonium sulfate or sulfonate charge control agents for electrophotographic developers compatible with viton fuser |
| US4464450A (en) | 1982-09-21 | 1984-08-07 | Xerox Corporation | Multi-layer photoreceptor containing siloxane on a metal oxide layer |
| US4560635A (en) | 1984-08-30 | 1985-12-24 | Xerox Corporation | Toner compositions with ammonium sulfate charge enhancing additives |
| US4587189A (en) * | 1985-05-24 | 1986-05-06 | Xerox Corporation | Photoconductive imaging members with perylene pigment compositions |
| US4921773A (en) | 1988-12-30 | 1990-05-01 | Xerox Corporation | Process for preparing an electrophotographic imaging member |
| US5164276A (en) | 1990-11-27 | 1992-11-17 | Xerox Corporation | Charge generation layers and charge transport, layers for electrophotographic imaging members, and processes for producing same |
| US5473064A (en) * | 1993-12-20 | 1995-12-05 | Xerox Corporation | Hydroxygallium phthalocyanine imaging members and processes |
| US5521306A (en) * | 1994-04-26 | 1996-05-28 | Xerox Corporation | Processes for the preparation of hydroxygallium phthalocyanine |
| US5482811A (en) * | 1994-10-31 | 1996-01-09 | Xerox Corporation | Method of making hydroxygallium phthalocyanine type V photoconductive imaging members |
| US5703487A (en) | 1996-01-11 | 1997-12-30 | Xerox Corporation | Detection of charge deficient spot susceptibility |
| US6150824A (en) | 1997-10-30 | 2000-11-21 | Xerox Corporation | Contactless system for detecting subtle surface potential charge patterns |
| US6008653A (en) | 1997-10-30 | 1999-12-28 | Xerox Corporation | Contactless system for detecting microdefects on electrostatographic members |
| DE60141562D1 (de) * | 2000-11-08 | 2010-04-29 | Ricoh Kk | Elektrophotographischer Photorezeptor, Verfahren zur Herstellung des Photorezeptors, und bildformendes Verfahren sowie Apparat worin der Photorezeptor eingesetzt wird |
| US7005222B2 (en) * | 2002-12-16 | 2006-02-28 | Xerox Corporation | Imaging members |
| US6913863B2 (en) * | 2003-02-19 | 2005-07-05 | Xerox Corporation | Photoconductive imaging members |
| US7291432B2 (en) * | 2004-03-23 | 2007-11-06 | Xerox Corporation | Imaging members |
| US7651827B2 (en) * | 2005-07-28 | 2010-01-26 | Xerox Corporation | Photoreceptor layer having phosphorus-containing lubricant |
| US7527902B2 (en) * | 2005-07-28 | 2009-05-05 | Xerox Corporation | Photoreceptor layer having solid and liquid lubricants |
| US7951514B2 (en) * | 2008-05-30 | 2011-05-31 | Xerox Corporation | Polymer anticurl backside coating (ACBC) photoconductors |
| US8012656B2 (en) * | 2008-05-30 | 2011-09-06 | Xerox Corporation | Backing layer containing photoconductor |
| US8062816B2 (en) * | 2008-05-30 | 2011-11-22 | Xerox Corporation | Phosphonate hole blocking layer photoconductors |
| US8048601B2 (en) * | 2008-05-30 | 2011-11-01 | Xerox Corporation | Aminosilane and self crosslinking acrylic resin hole blocking layer photoconductors |
| US7968261B2 (en) * | 2008-05-30 | 2011-06-28 | Xerox Corporation | Zirconocene containing photoconductors |
| US8003289B2 (en) * | 2008-05-30 | 2011-08-23 | Xerox Corporation | Ferrocene containing photoconductors |
| US8005410B2 (en) * | 2008-05-30 | 2011-08-23 | Xerox Corporation | Polyimide intermediate transfer components |
| US7985521B2 (en) * | 2008-05-30 | 2011-07-26 | Xerox Corporation | Anthracene containing photoconductors |
| US8012657B2 (en) * | 2008-05-30 | 2011-09-06 | Xerox Corporation | Phenol polysulfide containing photogenerating layer photoconductors |
-
2008
- 2008-05-30 US US12/129,969 patent/US7968263B2/en not_active Expired - Fee Related
-
2009
- 2009-03-12 EP EP09154999A patent/EP2128708B1/en not_active Expired - Fee Related
- 2009-05-25 JP JP2009124956A patent/JP2009288786A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| US20090297966A1 (en) | 2009-12-03 |
| EP2128708A1 (en) | 2009-12-02 |
| US7968263B2 (en) | 2011-06-28 |
| EP2128708B1 (en) | 2011-09-07 |
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Legal Events
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