US3569803A - Electrophotographic process utilizing friction charging - Google Patents
Electrophotographic process utilizing friction charging Download PDFInfo
- Publication number
- US3569803A US3569803A US752472A US3569803DA US3569803A US 3569803 A US3569803 A US 3569803A US 752472 A US752472 A US 752472A US 3569803D A US3569803D A US 3569803DA US 3569803 A US3569803 A US 3569803A
- Authority
- US
- United States
- Prior art keywords
- liquid
- friction
- image
- layer
- photoconductive
- 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.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims abstract description 38
- 239000007788 liquid Substances 0.000 claims abstract description 30
- 239000002783 friction material Substances 0.000 claims abstract description 11
- 229920000742 Cotton Polymers 0.000 claims abstract description 7
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 24
- 239000000463 material Substances 0.000 claims description 14
- 239000011787 zinc oxide Substances 0.000 claims description 12
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 9
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 claims description 7
- 229910052980 cadmium sulfide Inorganic materials 0.000 claims description 7
- 229920002635 polyurethane Polymers 0.000 claims description 5
- 239000004814 polyurethane Substances 0.000 claims description 5
- 239000004408 titanium dioxide Substances 0.000 claims description 5
- 239000004677 Nylon Substances 0.000 claims description 3
- 229920000297 Rayon Polymers 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 239000013078 crystal Substances 0.000 claims description 3
- 229920001778 nylon Polymers 0.000 claims description 3
- 239000002964 rayon Substances 0.000 claims description 3
- 210000002268 wool Anatomy 0.000 claims description 3
- 239000005083 Zinc sulfide Substances 0.000 claims description 2
- 229910000011 cadmium carbonate Inorganic materials 0.000 claims description 2
- GKDXQAKPHKQZSC-UHFFFAOYSA-L cadmium(2+);carbonate Chemical compound [Cd+2].[O-]C([O-])=O GKDXQAKPHKQZSC-UHFFFAOYSA-L 0.000 claims description 2
- 239000010985 leather Substances 0.000 claims description 2
- 229910052984 zinc sulfide Inorganic materials 0.000 claims description 2
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 claims 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 abstract description 11
- 239000011230 binding agent Substances 0.000 abstract description 7
- 239000004744 fabric Substances 0.000 abstract description 6
- 230000004048 modification Effects 0.000 abstract description 5
- 238000012986 modification Methods 0.000 abstract description 5
- 239000000843 powder Substances 0.000 abstract description 5
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- 150000002148 esters Chemical class 0.000 description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 5
- 239000004593 Epoxy Substances 0.000 description 4
- 229920000180 alkyd Polymers 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 230000004300 dark adaptation Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- UQMZPFKLYHOJDL-UHFFFAOYSA-N zinc;cadmium(2+);disulfide Chemical compound [S-2].[S-2].[Zn+2].[Cd+2] UQMZPFKLYHOJDL-UHFFFAOYSA-N 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- IICCLYANAQEHCI-UHFFFAOYSA-N 4,5,6,7-tetrachloro-3',6'-dihydroxy-2',4',5',7'-tetraiodospiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C(C(=C(Cl)C(Cl)=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 IICCLYANAQEHCI-UHFFFAOYSA-N 0.000 description 1
- JCVDKAOETPMLTE-UHFFFAOYSA-L C([O-])([O-])=O.[Cd+2].[S-2].[Cd+2] Chemical compound C([O-])([O-])=O.[Cd+2].[S-2].[Cd+2] JCVDKAOETPMLTE-UHFFFAOYSA-L 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 230000000274 adsorptive effect Effects 0.000 description 1
- -1 alicyclic hydrocarbons Chemical class 0.000 description 1
- 239000001055 blue pigment Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- HGAZMNJKRQFZKS-UHFFFAOYSA-N chloroethene;ethenyl acetate Chemical compound ClC=C.CC(=O)OC=C HGAZMNJKRQFZKS-UHFFFAOYSA-N 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].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 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229930187593 rose bengal Natural products 0.000 description 1
- 229940081623 rose bengal Drugs 0.000 description 1
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
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
- G03G5/0542—Polyvinylalcohol, polyallylalcohol; Derivatives thereof, e.g. polyvinylesters, polyvinylethers, polyvinylamines
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/02—Sensitising, i.e. laying-down a uniform charge
- G03G13/025—Sensitising, i.e. laying-down a uniform charge by contact, friction or induction
-
- 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
-
- 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
- Y10S430/102—Electrically charging radiation-conductive surface
Definitions
- ABSTRACT A method for electro'statically charging the surface of a photoconductive insulative layer which is formed by dispersing an inorganic n-type photoconductive powder in a binder, which is primarily a vinyl chloride-vinyl acetate ELECTROPHOTOGHIC PROCESS UTILIZING FMQTION CHGING BACKGROUND OF Tl-IE INVENTION 1 Field of the Invention
- the present invention relates to an electrophotographic method for charging a photoconductive insulative layer utilizing friction.
- a corona discharge is commonly applied, and a charging method utilizing a simple mechanical device is also available, i.e., the surface of a recording layer is rubbed with an appropriate material to achieve triboelectric charging.
- a charging method utilizing a simple mechanical device is also available, i.e., the surface of a recording layer is rubbed with an appropriate material to achieve triboelectric charging.
- Such a method is described in US. Pat. No. 2,297,691.
- a photoconductive insulative layer comprising an ntype n-type photoconductive powder, such as ZnO, which is dispersed in a vinyl chloride vinyl acetate copolymer'with a composition ratio of vinyl chloride to vinyl acetate of from 95:5 to 55:45 parts by weight, is rubbed with a friction material, such as a cotton velvet cloth, to negatively charge the layer.
- a friction material such as a cotton velvet cloth
- the invention utilizes the differences in the triboelectric properties of the materials involved.
- the friction charging is performed while the surface of the insulative layer is maintained in contact with a highly insulative liquid, such as an aliphatic hydrocarbon.
- the invention thus has as its object the provision of a process which will yield an improved image of extremely high quality when developedDESCRIPTlON OF THE PREFERRED EMBODIMENTS
- a light sensitive layer comprising an n-type photoconductive semiconductor, such as photoconductive zinc oxide, titanium dioxide, ect., dispersed in a binder comprising a vinyl chloride-vinyl acetate copolymer as its main constituent, is rubbed with a friction material which is positive in the triboelectric series with respect to said layer, a copy which is superior in quality to other combinations can be obtained.
- Suitable prior art insulative binders for use with zinc oxide are poiysiloxane resins alkyd resins, epoxy esters, polyacrylic esters, polymethacrylic esters, styrene containing polymers, and the like. With respect to triboelectric characteristics, all of these resins are relatively positive, and powdery zinc oxide is extremely positive. Extremely positive "as used above, means that using ethylcellulose (ethoxized percentage: 47.5- 49.0 percent) as an empirically typical positively chargeable resin, zinc oxide is very positive in comparison. Nitrocellulose can be selected as a typical negatively chargeable resin.
- An image of high density is also hard to obtain even if an insulative material is applied as a supporting material or provides a relatively thick insulative layer between a conductive supporting material and a sensitive layer, or even where (for the purpose of minimizing the effect of leakage) an image-exposure is first applied to a light sensitive layer and its surface is then rubbed with a friction material in a liquid developer comprising an insulative liquid as carrier liquid.
- the binder used may contain a small quantity of plasticizer, but such a component is liable to stain the surface of a friction material when used repeatedly, and therefore it is preferably preferable that a plasticize not be used.
- plasticizer a component which may be present
- polymers of nonmigrating characteristics are desirable, for instance, vegetable oil modified alkyd resins, epoxy ester resins, vinyl monomer modified alkyd resin, and thelike, are available.
- a composition of 60 parts by weight of vinyl chloride-vinyl acetate copolymer and 40 parts of other components may be regarded as being the upper limit of binder composition. If a liquid development is utilized, it is desirable to cure the aforesaid alkyd resins, epoxy ester resins and the like by means of curing agent prior to development so as to improve the charge decay characteristics in the liquid.
- vinyl chloride vinyl acetate copolymer one containing more than 5 percent and less than 45 percent (by weight) vinyl acetate is suitable. It is difficult to dissolve polyvinyl chloride homopolymer in many solvents, while a content of more than 45 percent vinyl acetate lowers the insulating properties and the advantageous friction charge characteristic of polyvinyl chloride.
- a supporting material generally one possessing good conductivity may be used, but an insulative supporting material can be utilized when the friction step occurs after exposure.
- n-type photoconductive materials useful in the present invention there are titanium dioxide, zinc oxide, cadmium sulfide, cadmium sulfide-cadmium carbonate mixtures, cadmium sulfide-zinc sulfide mialed crystals, and the like. Mixtures of these substances may also be used.
- friction charging materials for the light sensitive material the most positive in comparison to a photoconductive layer in the triboelectric series are preferred
- proper mechanical properties are preferable. For instance, cotton velvet cloth, rayon, wool, tannedleathcr, nylon cloth, polyurethane sponge, and the like are especially desirable.
- an image with high resolution can be obtained by means of a liquid development, but this type of developing process is liable to be accompanied by fog in the image element background.
- this fog the following is a specially desirable modification of the present invention. Specifically, the friction generated between the friction material and the light sensitive layer is caused to take place under an insulative liquid. This process may be carried out either prior or subsequent to image exposure. If this method is followed, the fog density will be remarkably reduced.
- the mechanism of this aspect of the invention can be explained as of follows: when a thin layer of insulative liquid is formed on the surface of the light sensitive layer, the adhesion of toners to the surface of the light sensitive layer due to forces other than electrostatic forces (i.e., adsorptive attraction, trapping" into surface irregularities, etc.) in the subsequent developing process will be remarkably reduced.
- the charge acceptance of the light sensitive layer in the insulative liquid is higher than the carrier liquid of the developer, the lifetime" of a latent image will be extended, and the image 'density will be increased due to the presence of such a thin liquid layer.
- the liquid initially applied is a purified, highly insulative nonpolar liquid, and since the developer carried liquid contains resin and other components, the above requirement is satisfied.
- the liquid which is applied at the time of the generation of the friction should be such one that can be mixed with a developer which is applied subsequently and which will not attack a light sensitive layer.
- Typical examples are aliphatic hydrocarbons, alicyclic hydrocarbons and fluorinated hydrocarbons.
- the present invention makes an extremely simple electrography possible.
- the process may be practical in a compact copying machine and therefore it has a high value from an industrial viewpoint.
- the process of this invention (herein friction charging is employed) is more profitably used in an electrophotographic process in which the photoconductive layer is charged after the image-exposure, than in the process wherein a corona discharge is employed.
- This is due to the fact that when the photoconductive layer is image-exposed prior to charging and is then charged by a corona discharge utilizing a photoconductive after effect, sharp images will not usually be obtained.
- This result may be explained as follows: at the boundary of an exposed and an unexposed area, the conductivity of the former remains high, while the latter is low, so that when both of these ares areas are subjected to a corona discharge, the charge is barely accumulated in the former area, while the potential of the latter area absorbs the charge rapidly.
- the corona discharge is continued, this will cause the preferential deposition of corona-produced ions onto the exposed area, which will be repelled by the adjacent charged area which has the same polarity as the ions. Accordingly, the exposed areas which are adjacent the unexposed areas receive a higher concentration of con corona-produced ions and recover from light fatigue more rapidly than other exposed areas. Since such a phenomenon results immediately after the beginning of the charging by the corona, an image with an indefinite edge results.
- EXAMPLE 1 A light sensitive layer comprising 100 parts of photoconductive ZnO powder and 25 parts of vinyl chloride-vinyl acetate copolymer (containing 35 percent by weight of vinyl acetate) was coated to a thickness of 5 [LOB a sheet of paper which has had been rendered conductive. After the dark adaptation of the layer, an image exposure was applied by means of a contact exposure. The light sensitive paper was then clipped into a liquid developer comprising a paste of a kneaded mixture of phthalocyanine blue pigment and rosin-modified phenol-formaldehyde resin dispersed in cyclohexane. The surface of the light sensitive layer was then lightly rubbed several times with a polyurethane sponge.
- the pigment maintained a positive charge in the liquid, while the light sensitive layer which was rubbed with polyurethane was negatively charged. Thus, an attractive" development could be achieved.
- the resultant image was quite sharp, and showed no indistinct outline along the circumference of image as would be observed in an ordinary image involving the Kalmann method of electrophotography.
- the image density was also excellent.
- EXAMPLE 2 A light sensitive layer consisting of 50 parts of photocom ductive titanium dioxide, 50 parts of photoconductive zinc oxide, 27.5 parts of a vinyl chloride-vinyl acetate copolymer (the same type as used in example I) 2.5 parts of the epoxy ester of dehydrated castor oil fatty acid (oil length 40 percent and 10 parts per 1000 parts of rosebengal, was coated to a thickness of 5 p. on a sheet of the same type base paper as used in example 1.
- the surface of the light sensitive layer was rubbed several times with a piece of cotton velvet cloth and an image exposure was applied by the projection method.
- a positive line image was chosen as the original.
- the electrostatic latent image was developed by a cascade developer containing positivelycharged toners, and a positive reproduction of the original was obtained.
- cotton velvet cloth impregnated with purified kerosene was used to rub the surface of the light sensitive layer in the same manner as described above. After subsequent exposure and development, a homogeneous image with a low fog density was obtained.
- An electrophotographic method for electrostatically charging the surface of a photoconductive insulative layer formed by dispersing an inorganic n-type photoconductive powder in a binder comprising as its main constituent a vinyl chloride-vinyl acetate copolymer with a composition ratio of vinyl chloride to vinyl acetate ranging from about :5 to about 55:45 parts by weight which comprises rubbing said insulative layer with a friction material so as to produce a negative charge on the surface of said insulative layer by friction while maintaining a highly insulative liquid on the surface of said insulative layer so that the generated friction is caused to take place within the insulative liquid.
- n-type photoconductive material is selected from the group consisting of titanium dioxide, zinc oxide, cadmium sulfide, a mixture of cadmium sulfide and cadmium carbonate, and a mixed crystal of cadmium sulfide and zinc sulfide.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Photoreceptors In Electrophotography (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5231867 | 1967-08-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3569803A true US3569803A (en) | 1971-03-09 |
Family
ID=12911420
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US752472A Expired - Lifetime US3569803A (en) | 1967-08-15 | 1968-08-14 | Electrophotographic process utilizing friction charging |
Country Status (6)
Country | Link |
---|---|
US (1) | US3569803A (enrdf_load_stackoverflow) |
BE (1) | BE719365A (enrdf_load_stackoverflow) |
CA (1) | CA925561A (enrdf_load_stackoverflow) |
DE (1) | DE1797099A1 (enrdf_load_stackoverflow) |
FR (1) | FR1577647A (enrdf_load_stackoverflow) |
GB (1) | GB1232470A (enrdf_load_stackoverflow) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3804660A (en) * | 1970-08-17 | 1974-04-16 | Commw Of Australia | Dielectric recording on insulator surfaces |
US3941594A (en) * | 1970-09-09 | 1976-03-02 | Rank Xerox Ltd. | Electrophotographic element with ZnO and TiO2 |
US3969113A (en) * | 1971-10-28 | 1976-07-13 | Rank Xerox Ltd. | Photosensitive binder layer for xerography containing titanium oxide and a cadmium pigment |
US3971658A (en) * | 1973-03-14 | 1976-07-27 | Xerox Corporation | Imaging process employing friction charging in the presence of an electrically insulating liquid |
US5406356A (en) * | 1993-08-09 | 1995-04-11 | Lexmark International, Inc. | Liquid toner imaging with contact charging |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2297691A (en) * | 1939-04-04 | 1942-10-06 | Chester F Carlson | Electrophotography |
US2987660A (en) * | 1955-06-06 | 1961-06-06 | Haloid Xerox Inc | Xerographic charging |
US3052539A (en) * | 1953-10-01 | 1962-09-04 | Rca Corp | Electrostatic printing |
US3121006A (en) * | 1957-06-26 | 1964-02-11 | Xerox Corp | Photo-active member for xerography |
US3172024A (en) * | 1960-03-17 | 1965-03-02 | Xerox Corp | Charge induction |
-
1968
- 1968-08-10 CA CA027071A patent/CA925561A/en not_active Expired
- 1968-08-12 BE BE719365D patent/BE719365A/xx unknown
- 1968-08-14 US US752472A patent/US3569803A/en not_active Expired - Lifetime
- 1968-08-14 FR FR1577647D patent/FR1577647A/fr not_active Expired
- 1968-08-15 GB GB1232470D patent/GB1232470A/en not_active Expired
- 1968-08-16 DE DE19681797099 patent/DE1797099A1/de active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2297691A (en) * | 1939-04-04 | 1942-10-06 | Chester F Carlson | Electrophotography |
US3052539A (en) * | 1953-10-01 | 1962-09-04 | Rca Corp | Electrostatic printing |
US2987660A (en) * | 1955-06-06 | 1961-06-06 | Haloid Xerox Inc | Xerographic charging |
US3121006A (en) * | 1957-06-26 | 1964-02-11 | Xerox Corp | Photo-active member for xerography |
US3172024A (en) * | 1960-03-17 | 1965-03-02 | Xerox Corp | Charge induction |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3804660A (en) * | 1970-08-17 | 1974-04-16 | Commw Of Australia | Dielectric recording on insulator surfaces |
US3941594A (en) * | 1970-09-09 | 1976-03-02 | Rank Xerox Ltd. | Electrophotographic element with ZnO and TiO2 |
US3969113A (en) * | 1971-10-28 | 1976-07-13 | Rank Xerox Ltd. | Photosensitive binder layer for xerography containing titanium oxide and a cadmium pigment |
US3971658A (en) * | 1973-03-14 | 1976-07-27 | Xerox Corporation | Imaging process employing friction charging in the presence of an electrically insulating liquid |
US5406356A (en) * | 1993-08-09 | 1995-04-11 | Lexmark International, Inc. | Liquid toner imaging with contact charging |
Also Published As
Publication number | Publication date |
---|---|
BE719365A (enrdf_load_stackoverflow) | 1969-01-16 |
DE1797099A1 (de) | 1971-11-11 |
FR1577647A (enrdf_load_stackoverflow) | 1969-08-08 |
CA925561A (en) | 1973-05-01 |
GB1232470A (enrdf_load_stackoverflow) | 1971-05-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3041167A (en) | Xerographic process | |
US3666363A (en) | Electrophotographic process and apparatus | |
US3573906A (en) | Electrophotographic plate and process | |
US3575505A (en) | Automatic bias control | |
US2965481A (en) | Electrostatic charging and image formation | |
US3649262A (en) | Simultaneous development-cleaning of the same area of an electrostatographic image support surface | |
JP3155915B2 (ja) | 画像形成装置 | |
US3615395A (en) | Electrostatic and electrophotographic variable contrast image-forming methods | |
US3216844A (en) | Method of developing electrostatic image with photoconductive donor member | |
US2954291A (en) | Method for preparing a spirit duplicating master | |
US2990280A (en) | Electrostatic printing | |
US3719481A (en) | Electrostatographic imaging process | |
JPS6148150B2 (enrdf_load_stackoverflow) | ||
US3569803A (en) | Electrophotographic process utilizing friction charging | |
JPH02141761A (ja) | 電子写真装置 | |
US3928036A (en) | Flexible xerographic photoreceptor element | |
US3764315A (en) | Ambipolar electrophotographic plate | |
CA1044067A (en) | Use of fluorinated resins to tailor the triboelectric properties of photoconductive insulating layers | |
US3926824A (en) | Electrostatographic developer composition | |
US3540885A (en) | Reduction of fog formation in an electrophotographic light sensitive sheet | |
US4551003A (en) | Electrophotographic process and apparatus therefor | |
US5686214A (en) | Electrostatographic imaging members | |
US4600668A (en) | Electrophotographic process | |
US4060415A (en) | Electrophotographic process | |
US4038076A (en) | Process for producing electrostatographic prints |