US3438773A - Flexible transparent electrophotographic film and method of development of said film - Google Patents
Flexible transparent electrophotographic film and method of development of said film Download PDFInfo
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- US3438773A US3438773A US492695A US3438773DA US3438773A US 3438773 A US3438773 A US 3438773A US 492695 A US492695 A US 492695A US 3438773D A US3438773D A US 3438773DA US 3438773 A US3438773 A US 3438773A
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- 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
- G03G5/14—Inert intermediate or cover layers for charge-receiving layers
- G03G5/142—Inert intermediate layers
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- 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
- G03G13/06—Developing
- G03G13/08—Developing using a solid developer, e.g. powder developer
- G03G13/09—Developing using a solid developer, e.g. powder developer using magnetic brush
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- 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
- G03G5/10—Bases for charge-receiving or other layers
- G03G5/104—Bases for charge-receiving or other layers comprising inorganic material other than metals, e.g. salts, oxides, carbon
-
- 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
- G03G5/14—Inert intermediate or cover layers for charge-receiving layers
- G03G5/147—Cover layers
- G03G5/14708—Cover layers comprising organic material
- G03G5/14713—Macromolecular material
- G03G5/14717—Macromolecular material obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G5/14721—Polyolefins; Polystyrenes; Waxes
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- 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
- G03G5/14—Inert intermediate or cover layers for charge-receiving layers
- G03G5/147—Cover layers
- G03G5/14708—Cover layers comprising organic material
- G03G5/14713—Macromolecular material
- G03G5/14717—Macromolecular material obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G5/14726—Halogenated polymers
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- 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
- G03G5/14—Inert intermediate or cover layers for charge-receiving layers
- G03G5/147—Cover layers
- G03G5/14708—Cover layers comprising organic material
- G03G5/14713—Macromolecular material
- G03G5/14717—Macromolecular material obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G5/1473—Polyvinylalcohol, polyallylalcohol; Derivatives thereof, e.g. polyvinylesters, polyvinylethers, polyvinylamines
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- 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
- G03G5/14—Inert intermediate or cover layers for charge-receiving layers
- G03G5/147—Cover layers
- G03G5/14708—Cover layers comprising organic material
- G03G5/14713—Macromolecular material
- G03G5/14747—Macromolecular material obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- G03G5/1476—Other polycondensates comprising oxygen atoms in the main chain; Phenol resins
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/10—Developers with toner particles characterised by carrier particles
- G03G9/107—Developers with toner particles characterised by carrier particles having magnetic components
- G03G9/1075—Structural characteristics of the carrier particles, e.g. shape or crystallographic structure
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/10—Developers with toner particles characterised by carrier particles
- G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
- G03G9/1132—Macromolecular components of coatings
- G03G9/1133—Macromolecular components of coatings obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/1134—Macromolecular components of coatings obtained by reactions only involving carbon-to-carbon unsaturated bonds containing fluorine atoms
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/10—Developers with toner particles characterised by carrier particles
- G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
- G03G9/1132—Macromolecular components of coatings
- G03G9/1135—Macromolecular components of coatings obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/1136—Macromolecular components of coatings obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon atoms
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- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
- Y10T428/2998—Coated including synthetic resin or polymer
Definitions
- the present invention is concerned with electrophotographic materials, i.e. materials useful in carrying out electrophotographic processes.
- the present invention is concerned with the constitution of electrophotographic films having a high transmittance and with toner compositions applicable to said films for the purpose of visible presentation of latent electrostatic images.
- Electrostatic processes for graphic reproduction and photography have been developed by many investigators for a long period of time, their goals being mainly limited to graphic reproductions on opaque papers.
- the bestknown system, called xerography has been disclosed in Journal of the Optical Society of America, vol. 38, No. 12, December 1948.
- transparent photography by an electrostatic process has not been achieved successfully, for the reason that transparent photographs, usually projected in large magnification onto a screen, require higher resolution, less fog and an exact reproduction covering half tone.
- the toner consist of finely dispersed pigment powder.
- Prior toner compositions, usually containing resin binder have a tendency to aggregate during developing and fixing.
- FIG. 1 is a cross-sectional view, on a highly exaggerated scale, of a transparent electrophotographic film in accordance with this invention
- FIG. 2 is a graphical illustration of an effect of additive amount of surface active agent on the charge intensities of toners in accordance with this invention.
- a transparent conductive layer 2 is coated on a transparent film base 1, and is laminated firmly to an organic photoconductive layer 4 through the medium of an adhesive 3.
- the organic photoconductive layer 4 is coated with a transparent resin 5 having a tonerfixing capacity Which is established upon curing the resin by heating or by treating with vapors of an appropriate organic solvent.
- the film is provided with a top coat layer 5 which fixes an imaged toner pigment.
- electrophotographic film comprising a top coat layer for fixing is not known; moreover, the toner itself has heretofore contained a resin for fixing imaged pigment.
- a top coated layer of nonphotoconductive material on the photoconductive material layer would act to lower the electrophotographic light sensitivity and the resolution of image. It has been discovered, according to the present invention, that a suitable non-photoconductive material of the top coated layer does not lower the sensitivity and/or the resolution.
- the top coated layer consist of a resin which has a specific electrical resistivity higher than 10 ohmcm. and a thickness less than 15 and that it easily cures into a transparent layer for fixing a toner pig ment by means of heating or treating with vapors of a resin-soluble solvent.
- copolymer of vinyl chloride and vinyl acetate is preferable for the production of the top coated layer.
- the preferable thickness is of 5 to 10,.
- the transparent conductive layer is required to exhibit 60 to of transmittance in incandescence and a surface resistivity lower than 10 ohms.
- a thin layer of vacuum evaporated metal such as copper or chromium can be employed.
- a thin layer of cuprous iodide in a thickness of 200 to 800 m is most preferable for this purpose and can be prepared as follows: Copper is vacuum-evaporated on a sheet of commercial transparent cellulose acetate film and is iodized with iodine vapor in a similar way to that of the prior art; cf. method described in US. Pat. No. 2,756,165, patented July 24, 1956.
- the thickness of the cuprous iodide layer can be controlled by checking its transmittance. Any defects, such as pin holes and scratches, must be avoided because they give undesirable defects to resultant images.
- a transparent adhesive to laminate the cuprous iodide layer and organic photoconductive layer plays an important role on the quality of image.
- Polyvinyl acetate in a solvent inert to cuprous iodide and to the base material is preferable for obtaining an excellent resultant image, and is coated on the cuprous iodide layer by a per se Well known method, for example, by roller coating, spraying or squeezing in a thickness of 3 to 7p.
- the photoconductive layer can be formed of any material having photoconductivity characterized by a dark electric resistivity higher than 10 ohm-cm. It is necessary that the surface of the photoconductive layer be as smooth as that of plate glass.
- a thin layer of vacuum evaporated inorganic photoconductive material such as selenium or cadmium sulfide, can be employed but is of inferior transparency.
- Many organic materials having photoconductivity are superior to said inorganic materials from the standpoint of transparency.
- Organic polymeric materials such as p-oly-N-vinylcarbazole, polyacenaphthylene and polyvinyl triphenylpyrazoline can be employed without addition of binders.
- binders for formation of transparent thin layers oxadiazole compounds, leuco malachitegreen, tetrahydroimidazole deriva ives, pyrazoline derivatives, 4,5-diphenyl irnidazolthion derivatives and 1,3,4-triazole derivatives.
- the photoconductive layer be formed of poly-N-vinylcarbazole having incorporated therein a a small amount of Rhodamin 6G and Z-methyl-anthraquinone in a thickness of 20
- the coating method for the poly-N-vinylcarbazole solution is the same as that of polyvinyl acetate adhesive solution.
- the toner compositions of this invention are characterized by an elimination of i.e. absence of, resin for fixing the pigment powders.
- the toner comprises pigment powders and organic compounds which are employed to achieve uniform distribution of the electrostatic charge of the toner pigment. Since a conventional toner contains resin, such as coumarone-indene resin, piccopale resin or polystyrol, for fixing the pigment powders, these pigment powders have a tendency to aggregate during curing of the resin and result in an inferior image. This disadvantage is removed by using a top coated layer in the film constitution as described above and eliminating the resin in the toner compositions. This is a great feature of this invention.
- the toner is brushed onto the top coating layer having a latent electrostatic image by means of a magnetic brush which reveals the image immediately as the brush is swept across the top coated layer.
- the magnetic brush is per se art-known and consists of a permanent magnet carrying at one end a mass of iron powder loaded with the toner pigment. According to the present invention, it has been discovered that fogs of the visual images are reduced by using a toner pigment comprising fine powders of magnetic material.
- the magnetic brush picks up these powders and renders the resultant image clean when the magnetic force exceeds the Coulomb force.
- the operable magnetic materials in a fine powder form are (1) magnetic metal, such as iron, nickel, cobalt and their alloys, (2) magneitc oxide compound, such as magnetite, cobalt oxide (C 0 and ferrites, and (3) magnetic sulfide, such as FeS and C08.
- magnetic metal or alloy powder be coated with compound thereof such as oxide, hydroxide or sulfide for obtaining a high insulating coating by means of per se usual chemical techniques.
- the pigment be in a finely divided powder form of 0.5;; to 5 particle size.
- the preferable pigment consists of magnetite in 0.5 to 2, particle size in accordance with the present invention.
- the amount of electrostatic charge of pigment powder be high and be uniformly distributed throughout the powder and that there exist no positively charged pigment powder during the brushing process.
- Addition of surface active agents such as stearic acid or palmitic acid are known to be useful for this purpose.
- preferable surface active agents are fatty acids containing more than carbon atoms in the molecule. The more carbon atoms in the fatty acid, the more desirable the effect.
- the weight proportion of surface active agent to toner pigment is also required to be controlled.
- the preferable addition amount of stearic acid or palmitic acid is less than 5% by weight. An addition of more than 5% by weight of fatty acid results in an unhomogeneous mixture which produces undesirable images.
- the magnetic brush comprises a permanent magnet and a mass of iron powder called a carrier. It is of importance that the carrier be negatively charged and the toner pigment positively charged during brushing.
- the electrostatic process relating to the toner and the carrier has not yet been definitively clarified. It has been discovered according to the present invention that desirable amounts of negative charge of carrier are are satisfactorily achieved by coating the surface of the carrier iron powder with fiuorowax.
- preferable wax is poly trifluoro-chloro-ethylene wax having an average molecular weight of 1000 to 1300. Besides the preferable electrostatic properties, excellent lubricating properties between toner and carrier are also produced by applying the said wax in the developing process. From a consideration of fluidity, it is preferred that the carrier iron powder be in the form of spherical particles of 100 to 200 in diameter. A preferable weight proportion of trifluorochloro-ethylene polymer wax to the iron powder is 2 to 4% by weight.
- bonding of the fluorowax to the surface of the carrier iron powder is remarkably enhanced by treating the iron powder with a solution of free phosphoric acid, phosphate compound, such as ZnHPO or Na PO and a promoter, prior to the application of the fluor'owax.
- a solution of free phosphoric acid, phosphate compound such as ZnHPO or Na PO and a promoter
- the surface of the iron powder is firmly coated with a thin layer of Zn (PO which is not dissolved by any conventional solvents, such as water, alcohol or organic solvent, and is responsible for the strong adhesion of the fiuorowax.
- EXAMPLE l.-TO NER PREPARATION Metallic cobalt powder in an average particle size of 1.4 is heated at 800 C. in air to obtain a partly oxidized black powder.
- the black powder in an amount of 100 grams is immersed in 20 milliliters of benzene containing 0.5 gram of palmitic acid, and mixed sufficiently in a ball mill.
- the mixture in cream state is dried with hot air at 60 C., and is then evacuated in a vacuum chamber at room temperature (about 20 to about 30 C.) for about five hours, producing a toner free from benzene.
- EXAMPLE 2.-TONER PREPARATION A solution of 2.0 milliliters of ethanol and various amounts of stearic acid are added to 100 grams of magnetite in an average particle size of 0.2a and mixed in a ball mill. The magnetite is obtained by a per se well known chemical technique. The mixture in a cream state is dried with hot air at 60 C. and is then evacuated in a vacuum chamber at room temperature for about five hours, producing a toner free from ethanol.
- EXAMPLE 3.-CARRIER PREPARATION An aqueous solution of 3% by weight of sodium phosphate is added to 1 kilogram of electrolyzed iron powder in an average particle size of 100 to 200 The mixture is heated at C. for 30 minutes under stirring for cleaning the surface of the iron powder. After being washed with water, the cleaned powder is steeped in a hot aqueous solution of 3% by weight of monobasic zinc phosphate and 0.2% by weight of sodium nitrite.
- the iron powder in the solution is stirred for 50 minutes in 'order to form an active phosphate layer on the surface of the iron powder, and then is thoroughly washed with Water.
- the treated powder is steeped in an aqueous solution of 0.05% by weight of bichromic acid for 1 minute at room temperature and is quickly dried after being separated from the solution.
- Poly-trifiuoro-monochloro-ethylene having an average molecular weight of 1500 is added to 100 grams of the iron powder thus obtained.
- the mixture is heated at 80 C. with stirring. It is desirable for obtaining a homogeneous mixture to add 50 milliliters of methanol, which evaporates off completely during the mixing.
- EXAMPLE 4'COMPLETE EXEMPLARY PROCEDURE Metallic copper is evaporated onto a sheet of commercial cellulose diacetate film of 150 1. in thickness.
- the white light transmittance of evaporated film is 63%.
- the copper evaporated film is placed immediately in a glass chamber containing a small amount of crystalline iodine powder. As the air of the chamber is evacuated, there is a diminishing 'of the copper color, and finally the film becomes transparent.
- the transmittance of the cuprous iodide laminated film is 90% with white light and the surface resistance is ohm-cm.
- a toluene solution of by weight of polyvinyl acetate is coated onto said cuprous iodide film by a Baker type applicator and is dried thoroughly. The dried lacquering layer is 4 in thickness.
- Coating of both the photoconductive layer and the top layer is carried out in a manner similar to that of the polyvinyl acetate adhesive layer.
- the compositions of both solutions are given in Tables 1 and 2, respectively.
- the thickness of the two dried layers are 18 and 10 respectively.
- top layer Material Parts by weight Polyvinylchloride acetate 1 (top coating matrix) 100 Epoxy resin (plasticizer) 25 Chlorinated paraflin (plasticizer) l5 Methyl isobutyl ketone (solvent) 150 Toluene 350 1
- Polyvinylchloride acetate 1 top coating matrix
- Epoxy resin plasticizer
- Chlorinated paraflin plasticizer
- l5 Methyl isobutyl ketone
- Toluene 350 Commercially available e.g. under the trade name "AGH .C.
- the pale orange transparent electrophotographic film thus obtained is mounted on a 7 kv. corona generation apparatus and is charged up to 1000 negative volts in the dark, after which a static latent image of a subject to be reproduced is created by the conventional exposure method.
- the optimum exposure is 500 lux-sec.
- the developer consisting of one part by weight of toner and ten parts by weight of carrier, obtained by the process according to Example 2 and Example 3 respectively, is mixed thoroughly with a permanent magnetic stick and a magnetic brush is formed. By sweeping the brush onto said latent image, an excellent visual image is developed.
- the visual imaged film is placed in a glass chamber containing dense vapors of carbon tetrachloride for a period of time less than 2 seconds.
- the image is fixed stably.
- the resolution of the resultant fixed image is 50 lines per mm., and its reproduction of half tone is 7 steps by the Eastman Kodak No. 2 grey scale; and no fog is observed.
- An electrophotographic film capable of being developed by a magnetic brush, comprising, in lamination in the following order from the bottom up, a transparent polymer sheet, a transparent conductive layer, an organic photoconductive layer and a curable top coated resin layer which fixes a toner consisting of a pigment powder and a surface active agent and has a specific resistivity higher than 10 ohm-cm, said transparent conductive layer and said organic photoconductive layer being joined together by a transparent adhesive polyvinylacetate.
- top coated resin layer is formed of vinylchloride/vinylacetate copolymer in a thickness of 5 to 10 1.
- a method for electrophotographic reproduc ion comprising (1) sweeping a toner consisting of 1 to 5% by welght of surface active agent selected from the group consisting of stearic acid and palmitic acid and to 99% by Weight of magne ite of particle size less than 5n by means of a magnetic brush consisting of a permanent magnet and iron powder in a diameter of 100 to 200 which is coated initially with zinc phosphate and finally with poly-triflnoro-mono-chloro-ethylene wax onto an electrophotographic film consisting, in lamination, of a transparent polymer sheet, a transparent conductive layer of cuprous iodide, an organic photoconductive material layer and a top coated vinylchloride/vinylacetate copolymer, and (2) heating a combination of said film and said magnetically brushed toner thereon for fixing said magnetite powder.
- An transparent electrophoto raphic film comprising, in lamination in the following order from the bottom up, a transparent polymer backing sheet, a transparent electrically conductivelayer and a transparent layer of organic photoconductive material. said transparent conductlve layer and said organic photoconductive layer being oined together by a transparent layer of polyvinyl acetate adhesive.
- a transparent electrophotographic film comprising, 1n lamination in the following order from the bottom up, a transparent polymer backing sheet, a transparent electrically conductive layer, a transparent layer of organic photoconductive material and a curable top coated resin layer which fixes a visible-imaged fine powder without binder material and which is formed of vinylchloride/ vinylacetate copolymer in a thickness of 5 to 10p, said transparent conductive layer and said organic photoconductive insulating layer being joined together by a transparent layer of polyvinyl acetate adhesive.
- a method for electrophotographic reproduction comprising (1) sweeping a toner which contains no binder material by means of a magnetic brush consisting of a 7 8 magnetic magnet and iron powder onto a top coated 2,857,271 10/1958 Sugarman 961 surface of an electrophotographic film according to claim 2,986,467 5/1961 Kostelec et a1. 96-1 9, and (2) heating a combination of said top coated 3,338,710 8/1967 Goffe 96-1.1 surface and said magnetically brushed toner thereon for FOREIGN PATENTS fixing said toner. 5
- said transparent conductive layer is formed of cuprous Signed and sealed this 6th day of July 1971.
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Description
April 15, 1969 YOsH|K| HAYASHi ET AL 3,438,773
FLEXIBLE TRANSPARENT ELECTROPHOTOGRAPHIC FILM AND METHOD OF DEVELOPMENT OF SAID FILM- Filed 001'). l, 1965 5 TOP COATED LAYER PHOTO CONDUCTIVE LAYER ADHESIVE LAYER TRANSPARENT CONDUCTIVE LAYER FILM BASE AMOUNT OF STEARIC ACID IN MAGNETITE (WEIGHT PERCENTAGE) INVENTOR ATTORNEY;
United States Patent 3 438,773 FLEXIBLE TRANSPARENT ELECTROPHOTO- GRAPHIC FILM AND METHOD OF DE- VELOPMENT OF SAID FILM Yoshiki Hayashi, Hirakata-shi, and Hikofumi Oido, Osaka-fu, Japan, assignors to Matsushita Electric Industrial Co., Ltd., Osaka, Japan Filed Oct. 4, 1965, Ser. No. 492,695 Claims priority, application Japan, Oct. 2, 1964, 39/515,714; Oct. 29, 1964, 39/61,927; Nov. 9, 1964, 39/63,913; Mar. 26, 1965, 40/17,946
Int. Cl. G03g 5/06 US. Cl. 961.5 13 Claims ABSTRACT OF THE DISCLOSURE Flexible and transparent electrophotographic film characterized by less fog and high resolution covering half tone is prepared with a polyvinylacetate adhesive layer of from 3 to 7,u in thickness between a transparent conductive layer and an organic photoconductive layer. Toner is brushed onto a top coating layer having a latent electrostatic image by means of a magnetic brush which reveals an image immediately as the brush is swept across the top coated layer.
The present invention is concerned with electrophotographic materials, i.e. materials useful in carrying out electrophotographic processes.
More especially, the present invention is concerned with the constitution of electrophotographic films having a high transmittance and with toner compositions applicable to said films for the purpose of visible presentation of latent electrostatic images.
Electrostatic processes for graphic reproduction and photography have been developed by many investigators for a long period of time, their goals being mainly limited to graphic reproductions on opaque papers. The bestknown system, called xerography has been disclosed in Journal of the Optical Society of America, vol. 38, No. 12, December 1948. However, transparent photography by an electrostatic process has not been achieved successfully, for the reason that transparent photographs, usually projected in large magnification onto a screen, require higher resolution, less fog and an exact reproduction covering half tone. It is important for obtaining excellent images that the toner consist of finely dispersed pigment powder. Prior toner compositions, usually containing resin binder, have a tendency to aggregate during developing and fixing.
It is an object of the present invention to provide an electrophotographic image with high resolution, less fog and an exact reproduction covering half tone.
It is another object of the invention to provide compositions of toner producing visual images formed of finely dispersed particles.
It is a further object of the invention to provide transparent electrophotographic film constitutions characterized by less fog and high resolution covering half tone.
It is a still further object of the invention to provide a method of fixing toner in excellent images.
These and other objects of this invention will become apparent upon consideration of the following description taken together with accompanying drawings in which:
FIG. 1 is a cross-sectional view, on a highly exaggerated scale, of a transparent electrophotographic film in accordance with this invention, and FIG. 2 is a graphical illustration of an effect of additive amount of surface active agent on the charge intensities of toners in accordance with this invention.
Referring to FIG. 1, a transparent conductive layer 2 is coated on a transparent film base 1, and is laminated firmly to an organic photoconductive layer 4 through the medium of an adhesive 3. The organic photoconductive layer 4 is coated with a transparent resin 5 having a tonerfixing capacity Which is established upon curing the resin by heating or by treating with vapors of an appropriate organic solvent. It is an additional feature of this invention that the film is provided with a top coat layer 5 which fixes an imaged toner pigment. According to the prior art, electrophotographic film comprising a top coat layer for fixing is not known; moreover, the toner itself has heretofore contained a resin for fixing imaged pigment. It has heretofore been believed that a top coated layer of nonphotoconductive material on the photoconductive material layer would act to lower the electrophotographic light sensitivity and the resolution of image. It has been discovered, according to the present invention, that a suitable non-photoconductive material of the top coated layer does not lower the sensitivity and/or the resolution.
It is necessary that the top coated layer consist of a resin which has a specific electrical resistivity higher than 10 ohmcm. and a thickness less than 15 and that it easily cures into a transparent layer for fixing a toner pig ment by means of heating or treating with vapors of a resin-soluble solvent. According to the invention, copolymer of vinyl chloride and vinyl acetate is preferable for the production of the top coated layer. The preferable thickness is of 5 to 10,.
The transparent conductive layer is required to exhibit 60 to of transmittance in incandescence and a surface resistivity lower than 10 ohms. A thin layer of vacuum evaporated metal such as copper or chromium can be employed. A thin layer of cuprous iodide in a thickness of 200 to 800 m is most preferable for this purpose and can be prepared as follows: Copper is vacuum-evaporated on a sheet of commercial transparent cellulose acetate film and is iodized with iodine vapor in a similar way to that of the prior art; cf. method described in US. Pat. No. 2,756,165, patented July 24, 1956. The thickness of the cuprous iodide layer can be controlled by checking its transmittance. Any defects, such as pin holes and scratches, must be avoided because they give undesirable defects to resultant images.
A transparent adhesive to laminate the cuprous iodide layer and organic photoconductive layer plays an important role on the quality of image. Polyvinyl acetate in a solvent inert to cuprous iodide and to the base material is preferable for obtaining an excellent resultant image, and is coated on the cuprous iodide layer by a per se Well known method, for example, by roller coating, spraying or squeezing in a thickness of 3 to 7p.
The photoconductive layer can be formed of any material having photoconductivity characterized by a dark electric resistivity higher than 10 ohm-cm. It is necessary that the surface of the photoconductive layer be as smooth as that of plate glass. A thin layer of vacuum evaporated inorganic photoconductive material, such as selenium or cadmium sulfide, can be employed but is of inferior transparency. Many organic materials having photoconductivity are superior to said inorganic materials from the standpoint of transparency. Organic polymeric materials, such as p-oly-N-vinylcarbazole, polyacenaphthylene and polyvinyl triphenylpyrazoline can be employed without addition of binders. The following are operable only when accompanied by the addition of binders for formation of transparent thin layers: oxadiazole compounds, leuco malachitegreen, tetrahydroimidazole deriva ives, pyrazoline derivatives, 4,5-diphenyl irnidazolthion derivatives and 1,3,4-triazole derivatives. It
3 is preferable that the photoconductive layer be formed of poly-N-vinylcarbazole having incorporated therein a a small amount of Rhodamin 6G and Z-methyl-anthraquinone in a thickness of 20 The coating method for the poly-N-vinylcarbazole solution is the same as that of polyvinyl acetate adhesive solution.
In connection with the novel constitution of the electrophotographic film, the toner compositions of this invention are characterized by an elimination of i.e. absence of, resin for fixing the pigment powders. According to this invention, the toner comprises pigment powders and organic compounds which are employed to achieve uniform distribution of the electrostatic charge of the toner pigment. Since a conventional toner contains resin, such as coumarone-indene resin, piccopale resin or polystyrol, for fixing the pigment powders, these pigment powders have a tendency to aggregate during curing of the resin and result in an inferior image. This disadvantage is removed by using a top coated layer in the film constitution as described above and eliminating the resin in the toner compositions. This is a great feature of this invention.
The toner is brushed onto the top coating layer having a latent electrostatic image by means of a magnetic brush which reveals the image immediately as the brush is swept across the top coated layer. The magnetic brush is per se art-known and consists of a permanent magnet carrying at one end a mass of iron powder loaded with the toner pigment. According to the present invention, it has been discovered that fogs of the visual images are reduced by using a toner pigment comprising fine powders of magnetic material. When the toner contains pigment powders charged with an unfavorable sign or quantity or pigment powders free from electrostatic charge, the magnetic brush picks up these powders and renders the resultant image clean when the magnetic force exceeds the Coulomb force. The operable magnetic materials in a fine powder form are (1) magnetic metal, such as iron, nickel, cobalt and their alloys, (2) magneitc oxide compound, such as magnetite, cobalt oxide (C 0 and ferrites, and (3) magnetic sulfide, such as FeS and C08. In producing a toner pigment, it is desirable that the magnetic metal or alloy powder be coated with compound thereof such as oxide, hydroxide or sulfide for obtaining a high insulating coating by means of per se usual chemical techniques.
It is necessary that the pigment be in a finely divided powder form of 0.5;; to 5 particle size. The preferable pigment consists of magnetite in 0.5 to 2, particle size in accordance with the present invention.
Of importance is that the amount of electrostatic charge of pigment powder be high and be uniformly distributed throughout the powder and that there exist no positively charged pigment powder during the brushing process. Addition of surface active agents such as stearic acid or palmitic acid are known to be useful for this purpose. According to the invention, preferable surface active agents are fatty acids containing more than carbon atoms in the molecule. The more carbon atoms in the fatty acid, the more desirable the effect. The weight proportion of surface active agent to toner pigment is also required to be controlled. The preferable addition amount of stearic acid or palmitic acid is less than 5% by weight. An addition of more than 5% by weight of fatty acid results in an unhomogeneous mixture which produces undesirable images.
As described above, the magnetic brush comprises a permanent magnet and a mass of iron powder called a carrier. It is of importance that the carrier be negatively charged and the toner pigment positively charged during brushing. The electrostatic process relating to the toner and the carrier, however, has not yet been definitively clarified. It has been discovered according to the present invention that desirable amounts of negative charge of carrier are are satisfactorily achieved by coating the surface of the carrier iron powder with fiuorowax. The
preferable wax is poly trifluoro-chloro-ethylene wax having an average molecular weight of 1000 to 1300. Besides the preferable electrostatic properties, excellent lubricating properties between toner and carrier are also produced by applying the said wax in the developing process. From a consideration of fluidity, it is preferred that the carrier iron powder be in the form of spherical particles of 100 to 200 in diameter. A preferable weight proportion of trifluorochloro-ethylene polymer wax to the iron powder is 2 to 4% by weight. An application of trifluoro-monochloro-ethylene polymer wax to the carrier powder is made in a per se well-known manner, for example, the iron powder is immersed in the molten fluorowax or in a solution thereof in an inert solvent and subsequently dried.
Further, according to the present invention, bonding of the fluorowax to the surface of the carrier iron powder is remarkably enhanced by treating the iron powder with a solution of free phosphoric acid, phosphate compound, such as ZnHPO or Na PO and a promoter, prior to the application of the fluor'owax. When the iron powder is immersed into a solution of, for example, zinc phosphate, the surface of the iron powder is firmly coated with a thin layer of Zn (PO which is not dissolved by any conventional solvents, such as water, alcohol or organic solvent, and is responsible for the strong adhesion of the fiuorowax.
The following examples are given to illustrate presently preferred details of the invention, it being understood that the details of the examples are not to be taken as in any way limiting the invention thereto.
EXAMPLE l.-TO NER PREPARATION Metallic cobalt powder in an average particle size of 1.4 is heated at 800 C. in air to obtain a partly oxidized black powder. The black powder in an amount of 100 grams is immersed in 20 milliliters of benzene containing 0.5 gram of palmitic acid, and mixed sufficiently in a ball mill. The mixture in cream state is dried with hot air at 60 C., and is then evacuated in a vacuum chamber at room temperature (about 20 to about 30 C.) for about five hours, producing a toner free from benzene.
EXAMPLE 2.-TONER PREPARATION A solution of 2.0 milliliters of ethanol and various amounts of stearic acid are added to 100 grams of magnetite in an average particle size of 0.2a and mixed in a ball mill. The magnetite is obtained by a per se well known chemical technique. The mixture in a cream state is dried with hot air at 60 C. and is then evacuated in a vacuum chamber at room temperature for about five hours, producing a toner free from ethanol.
Referring to FIG. 2 wherein the charge intensity is represented in an arbitrary unit, it will be seen that the charge intensity increases with increase in the additive amount of stearic acid.
EXAMPLE 3.-CARRIER PREPARATION An aqueous solution of 3% by weight of sodium phosphate is added to 1 kilogram of electrolyzed iron powder in an average particle size of 100 to 200 The mixture is heated at C. for 30 minutes under stirring for cleaning the surface of the iron powder. After being washed with water, the cleaned powder is steeped in a hot aqueous solution of 3% by weight of monobasic zinc phosphate and 0.2% by weight of sodium nitrite.
The iron powder in the solution is stirred for 50 minutes in 'order to form an active phosphate layer on the surface of the iron powder, and then is thoroughly washed with Water. In order to increase the durability of the bonding, the treated powder is steeped in an aqueous solution of 0.05% by weight of bichromic acid for 1 minute at room temperature and is quickly dried after being separated from the solution. Poly-trifiuoro-monochloro-ethylene having an average molecular weight of 1500 is added to 100 grams of the iron powder thus obtained. The mixture is heated at 80 C. with stirring. It is desirable for obtaining a homogeneous mixture to add 50 milliliters of methanol, which evaporates off completely during the mixing.
EXAMPLE 4.'COMPLETE EXEMPLARY PROCEDURE Metallic copper is evaporated onto a sheet of commercial cellulose diacetate film of 150 1. in thickness. The white light transmittance of evaporated film is 63%. The copper evaporated film is placed immediately in a glass chamber containing a small amount of crystalline iodine powder. As the air of the chamber is evacuated, there is a diminishing 'of the copper color, and finally the film becomes transparent. The transmittance of the cuprous iodide laminated film is 90% with white light and the surface resistance is ohm-cm. A toluene solution of by weight of polyvinyl acetate is coated onto said cuprous iodide film by a Baker type applicator and is dried thoroughly. The dried lacquering layer is 4 in thickness.
Coating of both the photoconductive layer and the top layer is carried out in a manner similar to that of the polyvinyl acetate adhesive layer. The compositions of both solutions are given in Tables 1 and 2, respectively. The thickness of the two dried layers are 18 and 10 respectively.
Table 1.-Compositions of photosensitive layer Material: Parts by Weight Poly N vinylcarbazole 1 (photoconduc tive matrix) 100 Z-methyl-anthraquinone (sensitizer) 10 Rhodamine 6G (sensitizer) 0.04 Diphenyl chloride (plasticizer) 50 Toluene (solvent) 700 Poly-n-vinylcarbazole is commercially available e.g. as Luvican M-170; BASF. I
*See Schultz Farbstotttabellen," 71th edltion, 1st vol., 1931, p. 366, No. 866.
Table 2.-Compositions of top layer Material: Parts by weight Polyvinylchloride acetate 1 (top coating matrix) 100 Epoxy resin (plasticizer) 25 Chlorinated paraflin (plasticizer) l5 Methyl isobutyl ketone (solvent) 150 Toluene 350 1 Commercially available e.g. under the trade name "AGH .C.
2 Commercially available e.g. as Eplkote 828 Shell.
The pale orange transparent electrophotographic film thus obtained is mounted on a 7 kv. corona generation apparatus and is charged up to 1000 negative volts in the dark, after which a static latent image of a subject to be reproduced is created by the conventional exposure method. The optimum exposure is 500 lux-sec.
The developer consisting of one part by weight of toner and ten parts by weight of carrier, obtained by the process according to Example 2 and Example 3 respectively, is mixed thoroughly with a permanent magnetic stick and a magnetic brush is formed. By sweeping the brush onto said latent image, an excellent visual image is developed.
Finally the visual imaged film is placed in a glass chamber containing dense vapors of carbon tetrachloride for a period of time less than 2 seconds. The image is fixed stably. The resolution of the resultant fixed image is 50 lines per mm., and its reproduction of half tone is 7 steps by the Eastman Kodak No. 2 grey scale; and no fog is observed.
What is claimed is:
1. An electrophotographic film, capable of being developed by a magnetic brush, comprising, in lamination in the following order from the bottom up, a transparent polymer sheet, a transparent conductive layer, an organic photoconductive layer and a curable top coated resin layer which fixes a toner consisting of a pigment powder and a surface active agent and has a specific resistivity higher than 10 ohm-cm, said transparent conductive layer and said organic photoconductive layer being joined together by a transparent adhesive polyvinylacetate.
2. An electrophotographic film according to claim 1, wherein said top coated resin layer is formed of vinylchloride/vinylacetate copolymer in a thickness of 5 to 10 1..
3. An electrophotographic film according to claim 1, chloride vinylacetate copolymer in a thickness of 5 to lO t. cuprous iodide in a thickness of 200 rm to 800 m 4. An electrophotographic film according to claim 1, wherein said transparent adhesive is formed of polymer of vinyl acetate in a thickness of 3 to 7 5. An electrophotographic film according to claim 1, wherein said top coated resin layer is formed of vinylchloride/vinylacetate copolymer in a thickness of 7a, said transparent conductive layer is formed of cuprous iodide in a thickness of 400 m with a transmittance of percent by incandescence, and said transparent adhesive layer is formed of polymer of vinyl acetate in a thickness of 5a.
6. A method for electrophotographic reproduc ion comprising (1) sweeping a toner consisting of 1 to 5% by welght of surface active agent selected from the group consisting of stearic acid and palmitic acid and to 99% by Weight of magne ite of particle size less than 5n by means of a magnetic brush consisting of a permanent magnet and iron powder in a diameter of 100 to 200 which is coated initially with zinc phosphate and finally with poly-triflnoro-mono-chloro-ethylene wax onto an electrophotographic film consisting, in lamination, of a transparent polymer sheet, a transparent conductive layer of cuprous iodide, an organic photoconductive material layer and a top coated vinylchloride/vinylacetate copolymer, and (2) heating a combination of said film and said magnetically brushed toner thereon for fixing said magnetite powder.
7. A method for electrophotographic reprodutcion according to claim 6, wherein said fixing of magnetite powder is effected by treating said combination of film and toner with vapors of an organic solvent for said copolymer.
8. An transparent electrophoto raphic film comprising, in lamination in the following order from the bottom up, a transparent polymer backing sheet, a transparent electrically conductivelayer and a transparent layer of organic photoconductive material. said transparent conductlve layer and said organic photoconductive layer being oined together by a transparent layer of polyvinyl acetate adhesive.
9. A transparent electrophotographic film comprising, 1n lamination in the following order from the bottom up, a transparent polymer backing sheet, a transparent electrically conductive layer, a transparent layer of organic photoconductive material and a curable top coated resin layer which fixes a visible-imaged fine powder without binder material and which is formed of vinylchloride/ vinylacetate copolymer in a thickness of 5 to 10p, said transparent conductive layer and said organic photoconductive insulating layer being joined together by a transparent layer of polyvinyl acetate adhesive.
10. An electrophotographic film according to claim 8 wherein the polyvinyl acetate adhesive layer is from 3 to 7 in thickness.
11. An electrophotographic film according to claim 9 wherein the polyvinyl acetate adhesive layer is from 3 to 7 in thickness.
12. A method for electrophotographic reproduction comprising (1) sweeping a toner which contains no binder material by means of a magnetic brush consisting of a 7 8 magnetic magnet and iron powder onto a top coated 2,857,271 10/1958 Sugarman 961 surface of an electrophotographic film according to claim 2,986,467 5/1961 Kostelec et a1. 96-1 9, and (2) heating a combination of said top coated 3,338,710 8/1967 Goffe 96-1.1 surface and said magnetically brushed toner thereon for FOREIGN PATENTS fixing said toner. 5
13. A method for electrophotographic image reproduc- 598,591 12/1960 Belglumtion according to claim 12, wherein said fixing of toner OTHER REFERENCES is effected by treating said combination of film and toner with vapors of organic solvent which can soften said gi g g g ii zg gji translated by top coated surface. 10 p References Cited J. TRAVIS BROWliI, Primary Examiner. UNITED STATES PATENTS J. C. COPPER, Assistant Examiner.
2,663,636 12/1953 Middleton 961 US. Cl. X.R.
2,756,165 7/1956 Lyon M 117211 15 96-1; 117 17.5
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,438,773 Dated April 15, 1969 l YOSHIKI HAYASHI and HIKOFUMI OIDO It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
- wherein said transparent conductive layer is formed of cuprous Signed and sealed this 6th day of July 1971.
(SEAL) Attest:
EDWARD M.FLETCHER,JR. WILLIAM E. SCHUYLER, JR. Attesting Officer Commissioner of Patents n r n l A r 1 n r s n a v n i n 1.
FORM FO-1050 [IO-59]
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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JP5671464 | 1964-10-02 | ||
JP6192764 | 1964-10-29 | ||
JP6391364 | 1964-11-09 | ||
JP1794665 | 1965-03-26 |
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US3438773A true US3438773A (en) | 1969-04-15 |
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US492695A Expired - Lifetime US3438773A (en) | 1964-10-02 | 1965-10-04 | Flexible transparent electrophotographic film and method of development of said film |
US00834181A Expired - Lifetime US3796664A (en) | 1964-10-02 | 1969-01-28 | Materials in electrophotographic process |
US834182*A Expired - Lifetime US3598648A (en) | 1964-10-02 | 1969-01-28 | Materials in electrophotographic process |
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Application Number | Title | Priority Date | Filing Date |
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US00834181A Expired - Lifetime US3796664A (en) | 1964-10-02 | 1969-01-28 | Materials in electrophotographic process |
US834182*A Expired - Lifetime US3598648A (en) | 1964-10-02 | 1969-01-28 | Materials in electrophotographic process |
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US (3) | US3438773A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3753709A (en) * | 1971-02-25 | 1973-08-21 | Eastman Kodak Co | Crosslinked resin overcoated electrophotographic elements useful in lithography |
FR2169326A1 (en) * | 1972-01-28 | 1973-09-07 | Addressograph Multigraph | |
US3909258A (en) * | 1972-03-15 | 1975-09-30 | Minnesota Mining & Mfg | Electrographic development process |
US3920453A (en) * | 1972-01-28 | 1975-11-18 | Addressograph Multigraph | Method of electrostatic duplicating by image transfer |
US4062681A (en) * | 1972-07-27 | 1977-12-13 | Eastman Kodak Company | Electrophotographic element having a hydrophobic, cured, highly cross-linked polymeric overcoat layer |
US4097617A (en) * | 1977-09-07 | 1978-06-27 | Addressograph-Multigraph Corporation | Phosphonitrile fluoroelastomer coated carrier particles for use in electrophotographic process |
US4173472A (en) * | 1976-06-15 | 1979-11-06 | Eastman Kodak Company | Polyester interlayer and binder component in multilayer photoconductive element |
US4191568A (en) * | 1977-03-15 | 1980-03-04 | Ricoh Co., Ltd. | Photosensitive material for electrophotography with dye containing overlayer |
US4284699A (en) * | 1977-02-14 | 1981-08-18 | Eastman Kodak Company | Polyester binder component in multilayer photoconductive element |
US4358519A (en) * | 1977-12-05 | 1982-11-09 | Honeywell Inc. | Technique of introducing an interface layer in a thermoplastic photoconductor medium |
US5512403A (en) * | 1994-08-05 | 1996-04-30 | Eastman Kodak Company | Mixture of carrier particles useful in electrographic developers |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3947271A (en) * | 1972-02-14 | 1976-03-30 | International Business Machines Corporation | Electrostatic imaging method using a polytetrafluoroethylene coated carrier particle |
US3922381A (en) * | 1974-06-14 | 1975-11-25 | Addressorgrap Multigraph Corp | Chemically treated carrier particles for use in electrophotographic process |
CA1080534A (en) * | 1976-01-23 | 1980-07-01 | Pitney-Bowes | Carrier particle with core of metal, sand or glass and coating of telomer of tetrafluoroethylene |
US4287281A (en) * | 1979-10-22 | 1981-09-01 | Xerox Corporation | Magnetic toner composition and a method of making the same |
JP2815613B2 (en) * | 1989-03-24 | 1998-10-27 | 株式会社リコー | Toner for developing electrostatic images |
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US2663636A (en) * | 1949-05-25 | 1953-12-22 | Haloid Co | Electrophotographic plate and method of producing same |
US2756165A (en) * | 1950-09-15 | 1956-07-24 | Dean A Lyon | Electrically conducting films and process for forming the same |
US2857271A (en) * | 1954-09-28 | 1958-10-21 | Rca Corp | Electrostatic printing process for producing photographic transparencies |
US2986467A (en) * | 1958-12-17 | 1961-05-30 | Gen Aniline & Film Corp | Photoconductive layer for recording element and method of producing same |
US3338710A (en) * | 1965-06-07 | 1967-08-29 | Xerox Corp | Frost thermography |
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US2663636A (en) * | 1949-05-25 | 1953-12-22 | Haloid Co | Electrophotographic plate and method of producing same |
US2756165A (en) * | 1950-09-15 | 1956-07-24 | Dean A Lyon | Electrically conducting films and process for forming the same |
US2857271A (en) * | 1954-09-28 | 1958-10-21 | Rca Corp | Electrostatic printing process for producing photographic transparencies |
US2986467A (en) * | 1958-12-17 | 1961-05-30 | Gen Aniline & Film Corp | Photoconductive layer for recording element and method of producing same |
BE598591A (en) * | 1959-12-28 | |||
US3338710A (en) * | 1965-06-07 | 1967-08-29 | Xerox Corp | Frost thermography |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3753709A (en) * | 1971-02-25 | 1973-08-21 | Eastman Kodak Co | Crosslinked resin overcoated electrophotographic elements useful in lithography |
FR2169326A1 (en) * | 1972-01-28 | 1973-09-07 | Addressograph Multigraph | |
US3920453A (en) * | 1972-01-28 | 1975-11-18 | Addressograph Multigraph | Method of electrostatic duplicating by image transfer |
US3909258A (en) * | 1972-03-15 | 1975-09-30 | Minnesota Mining & Mfg | Electrographic development process |
US4062681A (en) * | 1972-07-27 | 1977-12-13 | Eastman Kodak Company | Electrophotographic element having a hydrophobic, cured, highly cross-linked polymeric overcoat layer |
US4173472A (en) * | 1976-06-15 | 1979-11-06 | Eastman Kodak Company | Polyester interlayer and binder component in multilayer photoconductive element |
US4284699A (en) * | 1977-02-14 | 1981-08-18 | Eastman Kodak Company | Polyester binder component in multilayer photoconductive element |
US4191568A (en) * | 1977-03-15 | 1980-03-04 | Ricoh Co., Ltd. | Photosensitive material for electrophotography with dye containing overlayer |
US4097617A (en) * | 1977-09-07 | 1978-06-27 | Addressograph-Multigraph Corporation | Phosphonitrile fluoroelastomer coated carrier particles for use in electrophotographic process |
US4358519A (en) * | 1977-12-05 | 1982-11-09 | Honeywell Inc. | Technique of introducing an interface layer in a thermoplastic photoconductor medium |
US5512403A (en) * | 1994-08-05 | 1996-04-30 | Eastman Kodak Company | Mixture of carrier particles useful in electrographic developers |
Also Published As
Publication number | Publication date |
---|---|
US3796664A (en) | 1974-03-12 |
US3598648A (en) | 1971-08-10 |
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