EP0210868A1 - An organic photosensitive composition for electrophotography - Google Patents
An organic photosensitive composition for electrophotography Download PDFInfo
- Publication number
- EP0210868A1 EP0210868A1 EP86305899A EP86305899A EP0210868A1 EP 0210868 A1 EP0210868 A1 EP 0210868A1 EP 86305899 A EP86305899 A EP 86305899A EP 86305899 A EP86305899 A EP 86305899A EP 0210868 A1 EP0210868 A1 EP 0210868A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- parts
- weight
- photosensitive layer
- vinylcarbazole
- poly
- 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.)
- Withdrawn
Links
Images
Classifications
-
- 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
- G03G5/05—Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
- G03G5/0528—Macromolecular bonding materials
- G03G5/0532—Macromolecular bonding materials obtained by reactions only involving carbon-to-carbon unsatured bonds
- G03G5/0539—Halogenated polymers
-
- 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
- G03G5/07—Polymeric photoconductive materials
- G03G5/071—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G5/072—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising pending monoamine groups
- G03G5/073—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising pending monoamine groups comprising pending carbazole 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
- G03G5/05—Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
- G03G5/0528—Macromolecular bonding materials
- G03G5/0532—Macromolecular bonding materials obtained by reactions only involving carbon-to-carbon unsatured bonds
- G03G5/0546—Polymers comprising at least one carboxyl radical, e.g. polyacrylic acid, polycrotonic acid, polymaleic acid; Derivatives thereof, e.g. their esters, salts, anhydrides, nitriles, amides
Definitions
- This invention relates to an organic photosensitive composition for electrophotography which is superior in mechanical strength and which has an enhanced sensitivity.
- organic photosensitive materials poly-N-vinylcarbazole is generally used, but it is brittle so that the resulting photosensitive layer is inferior in abrasion-resistance.
- a conventional organic photosensitive material which contains poly-N-vinylcarbazole and polycarbonate as an additive functioning to improve the abrasion-resistance of the resulting photosensitive material is known, the abrasion-resistance is still insufficient, so that the organic photosensitive material cannot provide organic photosensitive compositions having excellent durability.
- the invention described herein makes possible the objects of (1) providing an organic photosensitive composition for electrophotography which is superior in mechanical strength; (2) providing an organic photosensitive composition for electrophotography from which a photosensitive layer having an extremely hard surface can be produced allowing for the minimization of a decrease in the surface potential of the photosensitive layer, resulting in a distinct and clear image; (3) providing an organic photosensitive composition for electrophotography which has an enhanced sensitivity; and (4) an organic photosensitive composition for electrophotography in which the reduction of the surface potential due to repeated light exposure is very much decreased.
- This invention provides a novel organic photosensitive layer having extremely superior abrasion-resistance and extremely high surface-hardness, compared with conventional photosensitive layers, notwithstanding that the photosensitive layer is made using vinylidene chloride-acrylonitrile copolymer which is neither hard nor binding. Therefore, resin materials having a high degree of hardness such as polycarbonate need not be used as an additive for improving a mechanical strength of poly-N-vinylcarbazole.
- vinylidene chloride-acrylonitrile copolymer is contained in an amount of 5 to 25 parts by weight, preferably 7 to 15 parts by weight, per 100 parts by weight of poly-N-vinylcarbazole.
- vinylidene chloride-acrylonitrile copolymer is contained in an amount of less than 5 parts by weight per 100 parts by weight of poly-N-vinylcarbazole, the resulting photosensitive layer has insufficient mechanical strength.
- Vinylidene chloride-acrylonitrile copolymer is synthesized by ordinal radical polymerization using radical polymerization initiators such as peroxides (e.g., benzoyl peroxide), azo-compounds (e.g., azobisisobutyronitrile), etc.
- radical polymerization initiators such as peroxides (e.g., benzoyl peroxide), azo-compounds (e.g., azobisisobutyronitrile), etc.
- known electron acceptors may be incorporated in an amount of 10 to 40 parts by weight, preferably 20 to 35 parts by weight, per 100 parts by weight of poly-N-vinylcarbazole.
- these electron acceptors chloranil, naphthoquinone, phthalic anhydride, nitrofluorenone, etc., can be used.
- the mixture was coated on an aluminum plate having a thickness of 80 ⁇ m by means of a wire bar and dried at 100°C for 1 hour, resulting in a photoconductor having a photosensitive layer thereon with a thickness of 14 ⁇ m.
- the photosensitive layer had a surface-hardness of 2H, which was determined by comparison with the hardness of pencils according to JIS (the Japanese Industrial Standards) scale of HB, F, H, 2H, ....
- the photoconductor was applied to an electrophotographic copying machine DC-191 (supplied by Mita Industrial Co., Ltd.) wherein an electrophotographic process was repeated 4 x 10 4 times.
- the accompanying figure shows the relationship between the aging cycle of the photosensitive layer and the thickness of the photosensitive layer, indicating that wear of the photosensitive layer of this invention was surprisingly minimized even though it was used in a electrophotographic copying machine for a long period of time, compared with a conventional photosensitive layer.
- the sensitivity of the photosensitive layer of this invention was 15 lux-second, which is the exposure quantity for half decay of the potential.
- the surface potentials of the photosensitive layer were 600 V and 550 V at the first and the 500th cycle, respectively. The difference therebetween was only 50 V, indicating that the reduction of the surface potential due to the repeated light exposure was surprisingly decreased (i.e., the aging characteristic is extremely improved).
- the residual potential of the photosensitive layer which was 20 V at the first, was largely retained even at the 500th cycle, indicating that the photosensitive layer supplied clear and distinct images over a long period of time.
- the sensitivity of the control photosensitive layer was about 32 lux ⁇ second, which contrasts strikingly with that of the photosensitive layer of this invention, 15 lux-second.
- the surface potential of the control photosensitive layer was 600 V at the first and it was almost unchanged even at the 500th cycle of a charging-discharging (exposure) process, but the residual potential of the control photosensitive layer, which was 100 V at the first, increased to 150 V at the 500th cycle.
- These values of the residual potential of the control layer are very much higher than that of the photosensitive layer of this invention, as low as 20 V.
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Photoreceptors In Electrophotography (AREA)
Abstract
An organic photosensitive composition for electrophotography comprising poly-N-vinylcarbazole as a charge-transfer medium and vinylidene chlorideacrylonitrile copolymer as an additive for improving the mechanical strength of said poly-N-vinylcarbazole.
Description
- This invention relates to an organic photosensitive composition for electrophotography which is superior in mechanical strength and which has an enhanced sensitivity.
- In order to obtain clear and distinct images, the surface of a photosensitive layer must be uniformly charged with static electricity. For this purpose, it is essential that the photosensitive layer is formed with a smoothness and an even thickness on the surface of a conductive substrate. Such a photosensitive layer is produced by a variety of inorganic or organic photosensitive materials. Inorganic photosensitive mate- rials provide a photosensitive layer the surface of which is hard and excellent in durability, so that they can be preferably used for photosensitive layers to be applied to large-scaled and high-speed copying machines. However, the inorganic photosensitive materials are expensive and some of them are harmful to human beings. Thus, in recent years, organic photosensitive materials are more popular than inorganic photosensitive materials for copying machines, especially low-speed copying machines.
- As organic photosensitive materials, poly-N-vinylcarbazole is generally used, but it is brittle so that the resulting photosensitive layer is inferior in abrasion-resistance. Although a conventional organic photosensitive material which contains poly-N-vinylcarbazole and polycarbonate as an additive functioning to improve the abrasion-resistance of the resulting photosensitive material is known, the abrasion-resistance is still insufficient, so that the organic photosensitive material cannot provide organic photosensitive compositions having excellent durability.
- Thus, wear of the photosensitive layer resulting from blade-cleaning and abrasion of the surface of the photosensitive layer resulting from paper-jamming cannot be prevented,
- In attempting to increase the mechanical strength of an organic photosensitive material such as poly-N-vinylcarbazole, the inventors of this invention discovered that the use of a gummy resin material as an additive can improve the mechanical strength of poly-N-vinylcarbazole. They finally succeeded in obtaining a novel organic photosensitive material having excellent abrasion-resistance and hardness.
- The organic photosensitive composition for electrophotography of this invention, which overcomes the above-discussed and numerous other disadvantages and deficiencies of the prior art, comprises poly-N-vinylcarbazole as a charge-transfer medium and vinylidene chloride-acrylonitrile copolymer as an additive for improving the mechanical strength of said poly-N-vinylcarbazole.
- The vinylidene chloride-acrylonitrile copolymer is, in a preferred embodiment, contained in an amount of 5 to 25 parts by weight per 100 parts by weight of poly-N-vinylcarbazole.
- The organic photosensitive composition further comprises, in a preferred embodiment, an electron acceptor in an amount of 10 to 40 parts by weight per 100 parts by weight of poly-N-vinylcarbazole and/or an electron donor in an amount of 10 to 60 parts by weight per 100 parts by weight of poly-N-vinylcarbazole.
- Thus, the invention described herein makes possible the objects of (1) providing an organic photosensitive composition for electrophotography which is superior in mechanical strength; (2) providing an organic photosensitive composition for electrophotography from which a photosensitive layer having an extremely hard surface can be produced allowing for the minimization of a decrease in the surface potential of the photosensitive layer, resulting in a distinct and clear image; (3) providing an organic photosensitive composition for electrophotography which has an enhanced sensitivity; and (4) an organic photosensitive composition for electrophotography in which the reduction of the surface potential due to repeated light exposure is very much decreased.
- This invention provides a novel organic photosensitive layer having extremely superior abrasion-resistance and extremely high surface-hardness, compared with conventional photosensitive layers, notwithstanding that the photosensitive layer is made using vinylidene chloride-acrylonitrile copolymer which is neither hard nor binding. Therefore, resin materials having a high degree of hardness such as polycarbonate need not be used as an additive for improving a mechanical strength of poly-N-vinylcarbazole.
- According to this invention, vinylidene chloride-acrylonitrile copolymer is contained in an amount of 5 to 25 parts by weight, preferably 7 to 15 parts by weight, per 100 parts by weight of poly-N-vinylcarbazole. When vinylidene chloride-acrylonitrile copolymer is contained in an amount of less than 5 parts by weight per 100 parts by weight of poly-N-vinylcarbazole, the resulting photosensitive layer has insufficient mechanical strength. When vinylidene chloride-acrylonitrile copolymer is contained in an amount of more than 25 parts by weight per 100 parts by weight of poly-N-vinylcarbazole, the content of poly-N-vinylcarbazole is relatively reduced so that poly-N-vinylcarbazole cannot sufficiently function as a charge-transfer medium.
- Vinylidene chloride-acrylonitrile copolymer is synthesized by ordinal radical polymerization using radical polymerization initiators such as peroxides (e.g., benzoyl peroxide), azo-compounds (e.g., azobisisobutyronitrile), etc.
- For the purpose of an enhancement of the sensitivity of the photosensitive layer and a decrease in the residual potential of the photosensitive layer, known electron acceptors may be incorporated in an amount of 10 to 40 parts by weight, preferably 20 to 35 parts by weight, per 100 parts by weight of poly-N-vinylcarbazole. As these electron acceptors, chloranil, naphthoquinone, phthalic anhydride, nitrofluorenone, etc., can be used.
- In order to further improve the sensitivity of the photosensitive layer and decrease the reduction of the surface potential of the photosensitive layer due to the repeated light exposure (i.e., to improve the aging characteristic), known electron donors, for example, phenanthren, diethyl aminophenylbenzaldehyde diphenylhydrazone, ethyl carbazolealdehyde diphenylhydrazone, triphenyl amine, etc., may be incorporated in an amount of 10 to 60 parts by weight, preferably 20 to 50 parts by weight, per 100 parts by weight of poly-N-vinylcarbazole.
- A vinylidene chloride-acrylonitrile copolymer synthesized by polymerization is dissolved in an appropriate solvent such as tetrahydrofuran, cyclohexane or the like, together with poly-N-vinylcarbazole and, as desired, an electron acceptor and/or an electron donor. The resulting solution is coated with a certain thickness on a conductive substrate, resulting in an organic photoconductor for electrophotography.
- One hundred parts by weight of poly-N-vinylcarbazole (manufactured by Anan Kohryo Co., Japan), 10 parts by weight of vinylidene chloride-acrylonitrile copolymer (Saran resin F-310; a number average molecular weight of 43,000; a weight average molecular weight of 120,000; manufactured by Asahi Dow Co.), 8 parts by weight of N,N'-di(3,5-dimethylphenyl)perylene-3,4,9,10-tetracarboxic acid diimide, 20 parts by weight of 2,3-dichloro-1,4-naphthoquinone, 40 parts by weight of phenanthrene,and 20 parts by weight of tetrahydrofuran were mixed in a stainless ball mill for 24 hours. The mixture was coated on an aluminum plate having a thickness of 80 µm by means of a wire bar and dried at 100°C for 1 hour, resulting in a photoconductor having a photosensitive layer thereon with a thickness of 14 µm. The photosensitive layer had a surface-hardness of 2H, which was determined by comparison with the hardness of pencils according to JIS (the Japanese Industrial Standards) scale of HB, F, H, 2H, ....
- The photoconductor was applied to an electrophotographic copying machine DC-191 (supplied by Mita Industrial Co., Ltd.) wherein an electrophotographic process was repeated 4 x 104 times.
- The accompanying figure shows the relationship between the aging cycle of the photosensitive layer and the thickness of the photosensitive layer, indicating that wear of the photosensitive layer of this invention was surprisingly minimized even though it was used in a electrophotographic copying machine for a long period of time, compared with a conventional photosensitive layer.
- The sensitivity of the photosensitive layer of this invention was 15 lux-second, which is the exposure quantity for half decay of the potential. The smaller the value of the exposure quantity for the half decay of the potential, the higher the sensitivity becomes. Moreover, the surface potentials of the photosensitive layer were 600 V and 550 V at the first and the 500th cycle, respectively. The difference therebetween was only 50 V, indicating that the reduction of the surface potential due to the repeated light exposure was surprisingly decreased (i.e., the aging characteristic is extremely improved). The residual potential of the photosensitive layer, which was 20 V at the first, was largely retained even at the 500th cycle, indicating that the photosensitive layer supplied clear and distinct images over a long period of time.
- One hundred parts by weight of poly-N-vinylcarbazole (manufactured by Anan Kohryo Co., Japan), 10 parts by weight of polycarbonate (panlight L manufactured by Teijin Co., Japan), 8 parts by weight of N,N'-di(3,5-dimethylphenyl)perylene-3,4,9,10-tetracar- boxic acid diimide, 20 parts by weight of 2,3-dichloro-1,4-naphthoquinone, 40 parts by weight of phenanthrene, and 20 parts by weight of tetrahydrofuran were mixed in a stainless ball mill for 24 hours.
- A control photoconductor was prepared usipg the mixture in the same manner as the photoconductor in the above-mentioned example. The surface-hardness of the photosensitive layer of the control photoconductor was determined to be F according to JIS.
- The photoconductor was applied to an electrophotographic copying machine in the same manner as in the above-mentioned example. The relationship between the aging cycle of the control photosensitive layer and the thickness of the control photosensitive layer is shown in the accompanying figure, indicating that the thickness of the control photosensitive layer was significantly reduced, while that of the photosensitive layer of this invention was almost unchanged. This means that the photoconductor of this invention is superior in abrasion-resistance and surface-hardness.
- Ten parts by weight of poly-N-vinylcarbazole (manufactured by Anan Kohryo Co., Japan), 10 parts by weight of polyester (biron 200 manufactured by Toyobo Co., Japan), 8 parts by weight of N,N'-di(3;5-dimethylphenyl)perylene-3,4,9,10-tetracarboxic acid diimide, 20 parts by weight of 2.3-dichloro-1,4-naphthoquinone, 40 parts by weight of phenanthrene, and 20 parts by weight of tetrahydrofuran were mixed in a stainless ball mill for 24 hours.
- A control photoconductor was prepared using the mixture in the same manner as in the above-mentioned example. The surface-hardness of the control photosensitive layer was determined to be F according to JIS, which indicates that the surface-hardness of the control photosensitive layer was inferior to that of the photosensitive layer of this invention.
- Preparation and examination were carried out in the same manner as in the above-mentioned example except that naphthoquinone was not used. The surface-hardness of the photosensitive layer of the resulting control photoconductor was 2H.
- However, the sensitivity of the control photosensitive layer was about 32 lux·second, which contrasts strikingly with that of the photosensitive layer of this invention, 15 lux-second. The surface potential of the control photosensitive layer was 600 V at the first and it was almost unchanged even at the 500th cycle of a charging-discharging (exposure) process, but the residual potential of the control photosensitive layer, which was 100 V at the first, increased to 150 V at the 500th cycle. These values of the residual potential of the control layer are very much higher than that of the photosensitive layer of this invention, as low as 20 V. These facts indicate that the sensitivity of the photosensitive layer of this invention containing an electron acceptor such as naphthoquinone is superior to that of the control layer lacking such an electron acceptor.
- Preparation and examination were carried out in the same manner as in the above-mentioned example except that phenanthrenewas not used. The surface-hardness of the photosensitive layer of the resulting control photoconductor was 2H. The sensitivity of the control photosensitive layer was 17 lux·second. The surface potentials of the control photosensitive layer, which were 600 V at the first, decreased to as low as 300 V at the 500th cycle, which contrasts strikingly with that of the photosensitive layer of this invention mentioned above. Moreover, the residual potential of the photosensitive layer from the first to the 500th cycle was aoproximately the same value, 40 V, which is somewhat higher than that of the photosensitive layer of this invention, 20V. These facts mean that the sensitivity of the photosensitive layer of this invention containing an electron donor such as phenanthrene is superior to that of the control layer lacking such an electron donor.
Claims (6)
1. An organic photosensitive composition for electrophotography comprising poly-N-vinylcarbazole as a charge-transfer medium and vinylidene chloride- acrylonitrile copolymer as an additive for improving the mechanical strength of said poly-N-vinylcarbazole.
2. An organic photosensitive composition for electrophotography according to claim 1, wherein said vinylidene chloride-acrylonitrile copolymer is contained in an amount of 5 to 25 parts by weight per 100 parts by weight of poly-N-vinylcarbazole.
3. An organic photosensitive composition for electrophotography according to claim 1, which further comprises an electron acceptor.
4. An organic photosensitive composition for electrophotography according to claim 1, 2 or 3, which further comprises an electron donor.
5. An organic photosensitive composition for electrophotography according to claim 3, wherein said electron acceptor is contained in an amount of 10 to 40 parts by weight per 100 parts by weight of poly-N-vinylcarbazole.
6. An organic photosensitive composition for electrophotography according to claim 4 or 5, wherein said electron donor is contained in an amount of 10 to 60 parts by weight per 100 parts by weight of poly-N-vinylcarbazole.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP170263/85 | 1985-07-31 | ||
| JP60170263A JPS6230253A (en) | 1985-07-31 | 1985-07-31 | Electrophotographic organic photosensitive body |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0210868A1 true EP0210868A1 (en) | 1987-02-04 |
Family
ID=15901692
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP86305899A Withdrawn EP0210868A1 (en) | 1985-07-31 | 1986-07-31 | An organic photosensitive composition for electrophotography |
Country Status (2)
| Country | Link |
|---|---|
| EP (1) | EP0210868A1 (en) |
| JP (1) | JPS6230253A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2649039B1 (en) * | 1989-06-30 | 1995-06-30 | Shachihata Industrial | RIGID PRINTING CHARACTER AND METHOD FOR PREPARING A RIGID POROUS MATERIAL USED FOR THE PRODUCTION THEREOF |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3917482A (en) * | 1970-11-09 | 1975-11-04 | Canon Kk | Photoconductive polymers of thiocyano-substituted-9-vinylcarbazoles |
| US3938994A (en) * | 1972-03-17 | 1976-02-17 | Eastman Kodak Company | Pyrylium dyes for electrophotographic composition and element |
| US4160666A (en) * | 1977-05-25 | 1979-07-10 | Eastman Kodak Company | Polymeric chemical sensitizers for organic photoconductive compositions |
| US4302522A (en) * | 1974-01-21 | 1981-11-24 | Garnett John L | Method of making polymeric photoconductive material involves partial polymerization step |
| DE3329054A1 (en) * | 1982-08-12 | 1984-02-16 | Canon K.K., Tokyo | LIGHT SENSITIVE RECORDING ELEMENT FOR ELECTROPHOTOGRAPHIC PURPOSES |
| US4451548A (en) * | 1981-03-13 | 1984-05-29 | Konishiroku Photo Industry Co., Ltd. | Electrophotographic photoreceptor |
-
1985
- 1985-07-31 JP JP60170263A patent/JPS6230253A/en active Pending
-
1986
- 1986-07-31 EP EP86305899A patent/EP0210868A1/en not_active Withdrawn
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3917482A (en) * | 1970-11-09 | 1975-11-04 | Canon Kk | Photoconductive polymers of thiocyano-substituted-9-vinylcarbazoles |
| US3938994A (en) * | 1972-03-17 | 1976-02-17 | Eastman Kodak Company | Pyrylium dyes for electrophotographic composition and element |
| US4302522A (en) * | 1974-01-21 | 1981-11-24 | Garnett John L | Method of making polymeric photoconductive material involves partial polymerization step |
| US4160666A (en) * | 1977-05-25 | 1979-07-10 | Eastman Kodak Company | Polymeric chemical sensitizers for organic photoconductive compositions |
| US4451548A (en) * | 1981-03-13 | 1984-05-29 | Konishiroku Photo Industry Co., Ltd. | Electrophotographic photoreceptor |
| DE3329054A1 (en) * | 1982-08-12 | 1984-02-16 | Canon K.K., Tokyo | LIGHT SENSITIVE RECORDING ELEMENT FOR ELECTROPHOTOGRAPHIC PURPOSES |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6230253A (en) | 1987-02-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4584253A (en) | Electrophotographic imaging system | |
| EP0187013B1 (en) | Photoconductive imaging member | |
| EP0186303A1 (en) | Electrophotographic imaging members | |
| DE3878181T2 (en) | ELECTROPHOTOGRAPHIC ELEMENT. | |
| CA2010564A1 (en) | Process for preparation of crystalline oxytitanium phthalocyanine | |
| US3634079A (en) | Substrate layer for dichroic photoconductors | |
| EP0210868A1 (en) | An organic photosensitive composition for electrophotography | |
| DE69535175T2 (en) | An electrophotographic photoreceptor and its use in an image forming process | |
| US3885961A (en) | Polymeric binder material for use in a photoconductive layer employed in electrophotography | |
| DE2355389A1 (en) | PHOTO-SENSITIVE BODY FOR ELECTROPHOTOGRAPHY | |
| US5550000A (en) | Process for producing electrophotographic photoreceptor | |
| US5192633A (en) | Laminate type photosensitive material for electrophotography | |
| GB2061541A (en) | Complex type electrophotographic plate and electrophotographic method using the same | |
| EP0402979A1 (en) | Electrophotographic recording material | |
| US3705032A (en) | Electrophotographic materials | |
| US5763126A (en) | Electrophotographic photoreceptor and production process for same | |
| US5460912A (en) | Electrophotography type lithographic form plate for laser beam | |
| US4376943A (en) | Record carrier for an electro-erosion printer and method for making same | |
| US6245471B1 (en) | Charge generation layers comprising at least one titanate and photoconductors including the same | |
| JP2000143788A (en) | Terminal blocked type polyester, its production and film formed product | |
| US4415642A (en) | Electrophotographic member of Se-Te-As with halogen | |
| US5116707A (en) | Laminated organic photosensitive material | |
| JPH0437762A (en) | Electrophotographic sensitive body | |
| AU622522B2 (en) | Process for preparation of crystalline oxytitanium phthalocyanine | |
| EP0738933B1 (en) | Photosensitive member and method of producing the same |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): DE FR GB NL |
|
| 17P | Request for examination filed |
Effective date: 19870223 |
|
| 17Q | First examination report despatched |
Effective date: 19880704 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
| 18D | Application deemed to be withdrawn |
Effective date: 19881115 |
|
| RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: NAKAZAWA, TORU Inventor name: AMAKAWA, YUUMI |