US3656990A - Electrosolography - Google Patents
Electrosolography Download PDFInfo
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- US3656990A US3656990A US483675A US3656990DA US3656990A US 3656990 A US3656990 A US 3656990A US 483675 A US483675 A US 483675A US 3656990D A US3656990D A US 3656990DA US 3656990 A US3656990 A US 3656990A
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- layer
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- electrostatic image
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- image
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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
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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
- G03G13/22—Processes involving a combination of more than one step according to groups G03G13/02 - G03G13/20
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G17/00—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process
- G03G17/10—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process using migration imaging, e.g. photoelectrosolography
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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
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
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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
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/08—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being inorganic
- G03G5/082—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being inorganic and not being incorporated in a bonding material, e.g. vacuum deposited
- G03G5/08207—Selenium-based
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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
- 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
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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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/138—Corona discharge process
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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
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
- Y10T428/263—Coating layer not in excess of 5 mils thick or equivalent
- Y10T428/264—Up to 3 mils
- Y10T428/265—1 mil or less
Definitions
- ABSTRACT An imaging member comprising a fracturable layer contacting a solvent soluble layer overlying a substrate, said fracturable layer spaced apart from said substrate is imaged by forming an electrostatic image on said member and then contacting said member with a solvent for said solvent soluble layer to form an imagewise pattern of material from said fracturable layer on said substrate.
- the imaging process disclosed employs a plate comprising an easily fracturable (usually particulate) photosensitive layer overlying a softenable plastic layer on a support substrate.
- the plate is first uniformly electrostatically charged in darkness and then exposed to an optical image to cause selective charge flow in the photosensitive layer.
- the photosensitive layer is selectively moved to the substrate surface in accordance with the optical image.
- the plate is immersed in a liquid solvent resulting in, in addition to the selective particle migration, the washing away of the photosensitive material in non-image areas along with the plastic layer itself.
- the aforementionedprocess requires the use of a consumable layer which is photosensitive, and it also requires control of activating radiation during certain steps of the process.
- the uniform electrostatic charge must usually be applied in darkness, and exposure to activating radiation is controlled until the image is developed.
- the degree of photosensitivity of the particular materials used must be taken into consideration in determining a suitable duration and intensity of exposure.
- a somewhat similar plate structure is used in the present invention, but its fracturable layer need not be photosensitive. Controlled migration of conductive or insulating particles may be effected without regard to lighting conditions.
- the present invention is also adaptable for use with reusable photoconductive layers and conventional xerographic plates, and other means for forming an electrostatic image on the consumable layer.
- the imaging plate used comprises a fracturable layer of conductive or insulating particles on or near the surface of a softenable plastic layer coated on a conductive substrate.
- An electrostatic charge pattern is formed on the fracturable layer in image configuration.
- portions of the fracturable layer migrate to the substrate surface in image configuration.
- the nonimaging portions of the fracturable layer are then removed along with the plastic layer.
- FIG. 1 is a schematic representation in cross-section of the imaging plate used in the present invention
- FIG. 2 is a schematic representation of electrostatic image formation on the imaging plate
- FIG. 3 is a schematic representation of an alternate method of electrostatic image formation
- FIG. 4 illustrates image development
- FIG. 5 illustrates dissolving away undesired plate materials
- FIG. 6 is a schematic representation in cross-section of an image produced in accordance with the present invention.
- FIG. 7 illustrates selective exposure of the softenable layer to ultra-violet radiation
- FIG. 8 illustrates cascading a particle-carrier mixture across the surface of the softenable layer
- FIG. 9 illustrates the application of a substantially uniform electrostatic charge to an imaging plate.
- FIG. 1 shows a cross-section of plate 10 according to the invention comprising a thin easily fracturable layer 11 overlying a softenable layer 12 in intimate contact with conductive substrate 13.
- Layer 11 is desirably sufficiently permeable to pennit applied solvent vapor to soften layer 12.
- Layer 11 should be easily fracturable, nevertheless, and most conveniently comprises a thin layer of finely divided particles which may be either electrically conductive or nonconductive.
- Fracturable layer refers to any layer 11 and specifically all the layer 11 forms disclosed herein, including those layers comprising discrete particles and those comprising apparently more mechanically continuous layers with a microscopic network of lines of mechanical weakness or which are otherwise fracturable and not completely mechanically coherent in the process hereof, which in the imaging member configurations hereof and their equivalents; in response to having an electrostatic image fonned thereon followed by solvent contact are caused to selectively deposit in image configuration on a substrate.
- Layer 12 is preferably a plastic which may be easily softened to permit selective migration of portions of layer 11 to the surface of substrate 13 under the influence of electrical forces. Also, layer 12 is preferably electrically nonconductive.
- Substrate 13 of plate 10 is normally an electrical conductor, but procedures adapted from the xerographic art permit the use of nonconductive substrates as well.
- Substrate 13 may conveniently be a metallic sheet, web, foil, cylinder or the like; a sheet of glass with an electrically conductive coating, preferably transparent; or a conductively coated sheet of paper or stable plastic such as polyethylene terephthalate.
- layer 12 may be formed by dip coating, roll coating, or vacuum evaporation, as well as other well-known techniques.
- layer 12 having a thickness of between 1 to 4 microns.
- layer 11 is preferably about 0.2 to 10 microns in thickness and may be deposited on the plastic layer in various ways.
- particles may be ground up and dusted onto layer 12, or finely divided particles may be mixed with larger granules of the type known as xerographic carrier and poured or cascaded over the surface of layer 12.
- layer 12 may be softened slightly by heating, for example, to permit particles deposited on its surface to sink a short distance into the plastic after which additional particles may be cascaded across or dusted over the plate.
- Other techniques may also be used for applying layer 11, such as softeningplastic layer 12 slightly to make it tacky, and then adhesively transferring imaging particles from a substantially uniformly coated donor sheet.
- layer 11 must retain an electrostatic charge during part of the instant process, it conveniently comprises particles that are electrically insulating. Conductive particles may be used, however, if lateral conductivity is minimized by loose packing, for example, or by partly embedding only a thin layer of particles in layer 12 so that neighboring particles are in poor electrical contact.
- Layer 11 may comprise any conductive or insulating particles (preferably micron or submicron sized) which do not dissolve in the solvent applied during the development step and which do not react with layer 12 in a way that would prevent particle migration to the substrate surface.
- photosensitive particles such as disclosed in the aforementioned application Ser. No. 460,377, may be used in the instant process if it is carried out in the substantial absence of actinic radiation. Generally, subdued lighting would meet this requirement.
- the thickness of layer 12 is not extremely critical. However, for a given material, thicker layers require the application of a higher charging voltage in carrying out the instant imaging process, and are, therefore, less desirable from the standpoint of employing the process with equipment of minimum cost and complexity. On the other hand, extremely thin layers are difiicult to form with a suitable degree of uniformity. Two microns has proven to be a generally suitable thickness for layer 12.
- any one of a variety of softenable materials may be used for layer 12, including thermoplastic type materials which have been used in electrostatic deformation imaging as described, for example, in application Ser. No. 193,277, filed May 8, 1962.
- suitable materials are: Staybelite Ester 10, a 50 per cent hydrogenated glycerol rosin ester of the Hercules Powder Company; Piccotex 100, a styrene-type resin of Pennsylvania Industrial Chemical Company; Araldite 6060 and 6071, epoxy resins of Ciba; and Velsicol X-37 (Velsicol Chemical Corp.)
- FIGS. 2-5 The basic process steps of the present invention are schematically represented in FIGS. 2-5.
- an electrostatic charge pattern conforming to the image to be reproduced is formed on layer 11 of plate 10, and layer 12 is then softened to permit selective migration of portions of layer 11 to the surface of substrate 13.
- layer 12 and the nonimaged portions of layer 11 are removed after the development step, whereby an image 11 resides on the surface of substrate 13 as shown in FIG. 6.
- FIG. 2 The formation of an electrostatic image on layer 11 is schematically shown in FIG. 2.
- a surface electrostatic charge pattern is applied through stencil 17 by means of corona discharge device 18.
- corona device 18 is raised to a high potential with respect to substrate 13 by means of power supply 19 as it is moved back and forth a few times in charging proximity with layer 11 to apply a sufficient charge.
- the configuration of the electrostatic image formed on layer 11 is determined by the perforations in stencil 17, as represented by the X at reference numeral 21.
- FIG. 3 Another method for forming an electrostatic image is shown in FIG. 3.
- a xerographic plate 30, comprising substrate 31 and photoconductive layer 32, on which an electrostatic image has been formed by conventional xerographic techniques is brought into direct contact with layer 11 while a substantially uniform electrostatic charge is applied to substrate 31 by means of corona device 28 connected to power supply 29.
- the polarity of the electrostatic charge applied by corona device 28 may be the same as or opposite to that of the latent electrostatic image on the surface of xerographic plate 30. This will depend upon whether a negative or positive image (in the photographic sense) is to be formed on the surface of substrate 13.
- an electrostatic charge pattern on layer 11 of plate may also be used.
- a shaped electrode may be positioned in close proximity to layer 11 and then pulsed with a high voltage with respect to substrate 13.
- the charge pattern may also be formed by means of a low energy electron beam. Still other methods such as those known to the art of xerography may also be applied.
- layer 12 is softened to permit selective migration of portions of layer 11 to the surface of substrate 13.
- FIG. 4 illustrates image development with a solvent for layer 12.
- solvent vapor 33 from container 32 is applied to the electrostatic image-bearing plate 10.
- the charged portions of layer 11 are found to adhere to the surface of substrate 13.
- plate 10 may be exposed to the solvent vapor for an indefinite period of time without deleterious effect on image quality.
- development time is not critical.
- portions of layer 11 remain on the surface of layer 12 and other portions, having selectively migrated, reside on the surface of the substrate.
- layer 12 is relatively thin, the resultant image, although useful in certain applications, is not readily discemable without special viewing means. Therefore, it is ordinarily desirable to remove the nonimaged portions of layer 11 along with plastic layer 12. This can be done, for example, by abrading away the unwanted materials, or, more conveniently, by immersing the platein a liquid solvent for layer 12, as illustrated in FIG. 5.
- FIG. 5 shows plate 10 immersed inliquid solvent 36 contained in tray 37.
- Layer. 12 is dissolved away and, deprived of mechanical support, the nonimaged portions of layer 11 disperse in the liquid leaving only the migrated portions of layer 11 on the substrate surface in image configuration.
- the electrostatic image formed on layer 11 may be developed by immersing the latent image-bearing plate in the liquid solvent directly.
- the liquid solvent should then be sufficiently electrically insulating to permit the charged portions of layer 11 to migrate to the surface of substrate 13 before the charge is dissipated by the liquid. If, on the other hand, vapor development precedes immersion in the liquid, the liquid need not be insulating. Migration having taken place before immersion, the washing away of unwanted materials by a conductive liquid will not deleteriously affect the image.
- the solvent used should be a solvent for layer 12, but not for layers 11 or 13.
- suitable solvents include, for example: cyclohexane, pentane, heptane, toluene, trichloroethylene, Sohio odorless solvent 3440 (Standard Oil Co. of Ohio), Freon 113 (E. I. duPont de Nemours Co., Inc.), and the like.
- FIG. 6 schematically represents the developed image in accordance with the present invention after removal of layer 12, and unwanted portions of layer 11.
- the migrated portions of layer 11, designated 11, are shown residing on the surface of substrate 13.
- a plate 10 is madeby first roll-coating a sheet of aluminized Mylar polyester film (E. l. duPont de Nemours Co., Inc.) with a layer of Piccotex (Pennsylvania Industrial Chemical Company) approximately 2 microns in thickness.
- a mixture of air spun graphite particles (Type 200-19, The Joseph Dixon Crucible Co., Jersey City, NJ.) and 50 micron glass beads is then cascaded across the surface of the resin layer to form a layer 13 (FIG. 1) approximately 1 micron in thickness.
- An electrostatic image is applied to the plate by means of a corona discharge device and a stencil, as illustrated in FIG. 2.
- the image areas are positively charged to about 60 volts.
- the latent image-bearing plate is then treated with cyclohexane vapor resulting in migration of the charged areas of layer 13 to the surface of the polyester film.
- Nonimaged portions of layer 13 and the layer of Piccotex 100 are then removed by immersing the developed plate in liquid cyclohexane for about 10 seconds. The result is a faithful visible replica of electrostatic image.
- Example I The procedure of Example I was carried out with a series of plates to which were applied electrostatic images of 2, 20, 40 and volts, respectively, instead of 60 volts as in Example I.
- faithful visible replicas of the electrostatic image were produced.
- the magnitude of the electrostatic image applied to the imaging plate is not critical as long as it is above the threshold to produce migration with the particular combination of materials used. As a practical matter, however, the magnitude of the electrostatic image applied will conveniently be far in excess of the threshold value. Generally, it is preferred to apply a potential of at least about 20 volts to assure high quality images. Below that value image contrast diminishes, but useful results are nevertheless produced.
- particle migration is controlled by an imagewise modification of the softenable layer prior to the above described development process.
- This approach obviates the formation of an electrostatic image and permits, instead, the use of a substantially uniform charge to impart the electrical forces required for particle migration. It also permits the use of electrically conductive particles without regard to lateral conductivity of layer 11.
- FIG. 7 showing the modification of the softenable layer by means of ultra-violet radiation.
- layer 12 of Staybelite 10 (2 microns in thickness) overlying aluminized Mylar substrate 13 is exposed for several minutes through image mask 21 to an image pattern of ultra-violet radiation from lamp 22.
- Layer 11 is then formed on layer 12 by cascading across it a mixture 41 of finely divided zinc oxide, or other marking particles and glass beads of the type suitable for xerographic carrier, as schematically illustrated in FIG. 8.
- the three-layer structure thereby formed is ready for the charging and developing steps for forming a visible image.
- actinic radiation may be used (either before or after formation of layer 11) to selectively modify the permeability of layer 12 to particle migration. Suitable methods include: X-ray treatment, Beta ray treatment, Gamma ray treatment and high energy electron bombardment.
- a substantially uniform electrostatic charge may be applied to layer 11 by moving corona discharge device 18 energized by high voltage power supply 19 in charging relation thereto.
- the corona device preferably applies a potential of at least about 20 volts to layer 11 with respect to substrate 13 to produce images of superior quality, especially as regards contrast.
- the instant process is operable, however, with much lower voltages, as the foregoing examples indicate.
- the charged plate may then be developed as described in connection with FIG. 4 and FIG. 5.
- An imaging method comprising the steps of:
- an imaging member comprising a fracturable layer contacting a solvent soluble layer overlying a substrate, said fracturable layer spaced apart from said substrate;
- An imaging method wherein the electrostatic image is formed on said imaging member by positioning a shaped electrode in close proximity to said member then pulsing said electrode with a high voltage.
- said fracturable layer comprises predominantly particles and is between about 0.2 to about 10 microns thick.
Abstract
An imaging member comprising a fracturable layer contacting a solvent soluble layer overlying a substrate, said fracturable layer spaced apart from said substrate is imaged by forming an electrostatic image on said member and then contacting said member with a solvent for said solvent soluble layer to form an imagewise pattern of material from said fracturable layer on said substrate.
Description
United States Patent U.S.Cl. ..117/l7.5, 1 17/8, 117/37 R, 96/1 R, 346/1, 204/181 Int. Cl. ..G03g 13/00 Field ofSearch ..96/1,1.3,1.4,1.5;117/17.5, 117/16, 29, 31, 33, 201, 265, 268, 72, 75, 132,
References Cited UNITED STATES PATENTS Mayo ..ll7/17.S
Goffe 1451 Apr. 18, 1972 154] ELECTROSOLOGRAPHY 2,901,374 8/1959 Gundlach ..117/17.5 2,924,519 2/1960 BefIelSIl...; ..96/l.4 [72] Invenmr- 2,968,553 1/1961 Gundlach ..96/1.4 [73] Assignee: Xerox Corporation, Rochester, NY. 2,996,400 8/1961 Rudd et al .117/17.5 I 3,121,006 '2/1964 Middleton m1 ..96/l.5 [221 Aug-3011965 3,154,415 10/1964 Kaulen ..96/38 x 21 Appl.No.: 483,675 3,166,432 1/1965 Gundlach.. ..117/17.5 3,254,997 6/1966 Schaffert ..96/1 Related Pp 3,284,224 11/1966 -Lehmann .117/175 3 318697 5/1967 Shrewsbu ..96/1
[63] Cont1nuat1on-1n-part of Ser. No. 403,002, Oct. 12, 1 1 Ty I 1964abandonad and a continuatiomimpart of 5 2,618,552 1l/l952 W188 .252/62.1 X N0. 460,377, June 1, 1965,1231. NO. 3,520,681,wh1ch 2,855,324 10/1958 is a continuationdmpart of N 403 002 2,909,443 10/1959 Wolll'lskl ..1 17/13 X 3,102,026 8/1963 Metcalfe et al ..96/1
Primary Examiner-Charles E. Van Horn Attorney-Stanley Z. Cole and James J. Ralabate [5 7] ABSTRACT An imaging member comprising a fracturable layer contacting a solvent soluble layer overlying a substrate, said fracturable layer spaced apart from said substrate is imaged by forming an electrostatic image on said member and then contacting said member with a solvent for said solvent soluble layer to form an imagewise pattern of material from said fracturable layer on said substrate.
8 Claims, 9 Drawing Figures ELECTROSOLOGRAPHY This application is a continuation-in-part of copending application Ser. No. 403,002, filed Oct. 12, 1964 now abandoned and a continuation-in-part of copending application Ser. No. 460,377 filed June 1, 1965 (now Goffe US. Pat. No. 3,520,681 which is a continuation-in-part of 403,002, and relates to a new imaging technique in which recording material is selectively moved through a softenable medium under the influence of electrical forces.
In the above-mentioned application and copending application Ser. No. 460,377, filed June 1, 1965, the imaging process disclosed employs a plate comprising an easily fracturable (usually particulate) photosensitive layer overlying a softenable plastic layer on a support substrate. According to one embodiment of that invention the plate is first uniformly electrostatically charged in darkness and then exposed to an optical image to cause selective charge flow in the photosensitive layer. Upon solvent or heat softening of the plastic layer, the photosensitive layer is selectively moved to the substrate surface in accordance with the optical image. Ordinarily, the plate is immersed in a liquid solvent resulting in, in addition to the selective particle migration, the washing away of the photosensitive material in non-image areas along with the plastic layer itself.
Thus, the aforementionedprocess requires the use of a consumable layer which is photosensitive, and it also requires control of activating radiation during certain steps of the process. The uniform electrostatic charge must usually be applied in darkness, and exposure to activating radiation is controlled until the image is developed. In addition, the degree of photosensitivity of the particular materials used must be taken into consideration in determining a suitable duration and intensity of exposure.
A somewhat similar plate structure is used in the present invention, but its fracturable layer need not be photosensitive. Controlled migration of conductive or insulating particles may be effected without regard to lighting conditions. The present invention is also adaptable for use with reusable photoconductive layers and conventional xerographic plates, and other means for forming an electrostatic image on the consumable layer.
Briefly summarizing the present invention in terms of a preferred embodiment: The imaging plate used comprises a fracturable layer of conductive or insulating particles on or near the surface of a softenable plastic layer coated on a conductive substrate. An electrostatic charge pattern is formed on the fracturable layer in image configuration. Upon softening of the plastic layer, for example by the application of a solvent therefor, portions of the fracturable layer migrate to the substrate surface in image configuration. Ordinarily, the nonimaging portions of the fracturable layer are then removed along with the plastic layer. Many variations of this process are within the scope of the present invention which is disclosed in detail in connection with the accompanying drawing.
In the drawing:
FIG. 1 is a schematic representation in cross-section of the imaging plate used in the present invention;
FIG. 2 is a schematic representation of electrostatic image formation on the imaging plate;
FIG. 3 is a schematic representation of an alternate method of electrostatic image formation;
FIG. 4 illustrates image development;
FIG. 5 illustrates dissolving away undesired plate materials;
FIG. 6 is a schematic representation in cross-section of an image produced in accordance with the present invention;
FIG. 7 illustrates selective exposure of the softenable layer to ultra-violet radiation;
FIG. 8 illustrates cascading a particle-carrier mixture across the surface of the softenable layer; and,
FIG. 9 illustrates the application of a substantially uniform electrostatic charge to an imaging plate.
Referring to the drawing, FIG. 1 shows a cross-section of plate 10 according to the invention comprising a thin easily fracturable layer 11 overlying a softenable layer 12 in intimate contact with conductive substrate 13.
Fracturable layer as used herein refers to any layer 11 and specifically all the layer 11 forms disclosed herein, including those layers comprising discrete particles and those comprising apparently more mechanically continuous layers with a microscopic network of lines of mechanical weakness or which are otherwise fracturable and not completely mechanically coherent in the process hereof, which in the imaging member configurations hereof and their equivalents; in response to having an electrostatic image fonned thereon followed by solvent contact are caused to selectively deposit in image configuration on a substrate.
Starting with substrate 13, any known method may be used to apply layer 12 substantially unifonn thickness. For example, layer 12 may be formed by dip coating, roll coating, or vacuum evaporation, as well as other well-known techniques. For most applications of the present invention, it has been found preferable to use a layer 12 having a thickness of between 1 to 4 microns.
For use in the present invention, layer 11 is preferably about 0.2 to 10 microns in thickness and may be deposited on the plastic layer in various ways. For example, particles may be ground up and dusted onto layer 12, or finely divided particles may be mixed with larger granules of the type known as xerographic carrier and poured or cascaded over the surface of layer 12. If thicker coatings are desired, layer 12 may be softened slightly by heating, for example, to permit particles deposited on its surface to sink a short distance into the plastic after which additional particles may be cascaded across or dusted over the plate. Other techniques may also be used for applying layer 11, such as softeningplastic layer 12 slightly to make it tacky, and then adhesively transferring imaging particles from a substantially uniformly coated donor sheet.
As layer 11 must retain an electrostatic charge during part of the instant process, it conveniently comprises particles that are electrically insulating. Conductive particles may be used, however, if lateral conductivity is minimized by loose packing, for example, or by partly embedding only a thin layer of particles in layer 12 so that neighboring particles are in poor electrical contact.
The thickness of layer 12 is not extremely critical. However, for a given material, thicker layers require the application of a higher charging voltage in carrying out the instant imaging process, and are, therefore, less desirable from the standpoint of employing the process with equipment of minimum cost and complexity. On the other hand, extremely thin layers are difiicult to form with a suitable degree of uniformity. Two microns has proven to be a generally suitable thickness for layer 12.
Any one of a variety of softenable materials may be used for layer 12, including thermoplastic type materials which have been used in electrostatic deformation imaging as described, for example, in application Ser. No. 193,277, filed May 8, 1962. Representative of suitable materials are: Staybelite Ester 10, a 50 per cent hydrogenated glycerol rosin ester of the Hercules Powder Company; Piccotex 100, a styrene-type resin of Pennsylvania Industrial Chemical Company; Araldite 6060 and 6071, epoxy resins of Ciba; and Velsicol X-37 (Velsicol Chemical Corp.)
The basic process steps of the present invention are schematically represented in FIGS. 2-5. In general, an electrostatic charge pattern conforming to the image to be reproduced is formed on layer 11 of plate 10, and layer 12 is then softened to permit selective migration of portions of layer 11 to the surface of substrate 13. Qptionally, but preferably for most applications of the present invention, layer 12 and the nonimaged portions of layer 11 are removed after the development step, whereby an image 11 resides on the surface of substrate 13 as shown in FIG. 6.
The formation of an electrostatic image on layer 11 is schematically shown in FIG. 2. According to the method illustrated, a surface electrostatic charge pattern is applied through stencil 17 by means of corona discharge device 18. Illustratively, corona device 18 is raised to a high potential with respect to substrate 13 by means of power supply 19 as it is moved back and forth a few times in charging proximity with layer 11 to apply a sufficient charge. The configuration of the electrostatic image formed on layer 11 is determined by the perforations in stencil 17, as represented by the X at reference numeral 21. v
Another method for forming an electrostatic image is shown in FIG. 3. According to this method, a xerographic plate 30, comprising substrate 31 and photoconductive layer 32, on which an electrostatic image has been formed by conventional xerographic techniques is brought into direct contact with layer 11 while a substantially uniform electrostatic charge is applied to substrate 31 by means of corona device 28 connected to power supply 29. The polarity of the electrostatic charge applied by corona device 28 may be the same as or opposite to that of the latent electrostatic image on the surface of xerographic plate 30. This will depend upon whether a negative or positive image (in the photographic sense) is to be formed on the surface of substrate 13.
Other methods of forming an electrostatic charge pattern on layer 11 of plate may also be used. For example, a shaped electrode may be positioned in close proximity to layer 11 and then pulsed with a high voltage with respect to substrate 13. The charge pattern may also be formed by means of a low energy electron beam. Still other methods such as those known to the art of xerography may also be applied.
After the electrostatic image has been formed on layer 11, layer 12 is softened to permit selective migration of portions of layer 11 to the surface of substrate 13.
FIG. 4 illustrates image development with a solvent for layer 12. As illustrated, solvent vapor 33 from container 32 is applied to the electrostatic image-bearing plate 10. As a result, the charged portions of layer 11 are found to adhere to the surface of substrate 13. As long as the solvent does not dissolve the material comprising layer 13, plate 10 may be exposed to the solvent vapor for an indefinite period of time without deleterious effect on image quality. Hence, development time is not critical.
At this stage in the instant process, portions of layer 11 remain on the surface of layer 12 and other portions, having selectively migrated, reside on the surface of the substrate. However, as layer 12 is relatively thin, the resultant image, although useful in certain applications, is not readily discemable without special viewing means. Therefore, it is ordinarily desirable to remove the nonimaged portions of layer 11 along with plastic layer 12. This can be done, for example, by abrading away the unwanted materials, or, more conveniently, by immersing the platein a liquid solvent for layer 12, as illustrated in FIG. 5.
FIG. 5 shows plate 10 immersed inliquid solvent 36 contained in tray 37. Layer. 12 is dissolved away and, deprived of mechanical support, the nonimaged portions of layer 11 disperse in the liquid leaving only the migrated portions of layer 11 on the substrate surface in image configuration.
It is noted that the electrostatic image formed on layer 11 may be developed by immersing the latent image-bearing plate in the liquid solvent directly. However, the liquid solvent should then be sufficiently electrically insulating to permit the charged portions of layer 11 to migrate to the surface of substrate 13 before the charge is dissipated by the liquid. If, on the other hand, vapor development precedes immersion in the liquid, the liquid need not be insulating. Migration having taken place before immersion, the washing away of unwanted materials by a conductive liquid will not deleteriously affect the image.
The solvent used should be a solvent for layer 12, but not for layers 11 or 13. Typically suitable solvents include, for example: cyclohexane, pentane, heptane, toluene, trichloroethylene, Sohio odorless solvent 3440 (Standard Oil Co. of Ohio), Freon 113 (E. I. duPont de Nemours Co., Inc.), and the like.
FIG. 6 schematically represents the developed image in accordance with the present invention after removal of layer 12, and unwanted portions of layer 11. Thus, the migrated portions of layer 11, designated 11, are shown residing on the surface of substrate 13.
The basic process can be further illustrated by means of the following examples.
An electrostatic image is applied to the plate by means of a corona discharge device and a stencil, as illustrated in FIG. 2. The image areas are positively charged to about 60 volts. The latent image-bearing plate is then treated with cyclohexane vapor resulting in migration of the charged areas of layer 13 to the surface of the polyester film. Nonimaged portions of layer 13 and the layer of Piccotex 100 are then removed by immersing the developed plate in liquid cyclohexane for about 10 seconds. The result is a faithful visible replica of electrostatic image.
EXAMPLES Il-V The procedure of Example I was carried out with a series of plates to which were applied electrostatic images of 2, 20, 40 and volts, respectively, instead of 60 volts as in Example I. Faithful visible replicas of the electrostatic image were produced.
EXAMPLES VI-XXII Applied Potential Solvent +40 volts Sohio odorless solvent 3440 +60 volts +90 volts +1 10 volts volts +40 volts +50 volts +60 volts +70 volts +80 volts +l volts +60 volts +150 volts 40 volts 50 volts l80 volts -300 volts cyclohexane Freon 1 l3 Sohio odorless solvent 3440 cyclohexane The instant imaging process has also been carried out with the materials and values shown in Table I. In each instance, the substrate comprised aluminized Mylar over which layer 12 was roll coated. Layer 11 was formed by the cascade method described above. Development was by immersion in solvent liquid. The garnet particles used had an average diameter of about 5 microns.
Cyclohexano.
Thus, the magnitude of the electrostatic image applied to the imaging plate is not critical as long as it is above the threshold to produce migration with the particular combination of materials used. As a practical matter, however, the magnitude of the electrostatic image applied will conveniently be far in excess of the threshold value. Generally, it is preferred to apply a potential of at least about 20 volts to assure high quality images. Below that value image contrast diminishes, but useful results are nevertheless produced.
According to another aspect of the present invention, particle migration is controlled by an imagewise modification of the softenable layer prior to the above described development process. This approach obviates the formation of an electrostatic image and permits, instead, the use of a substantially uniform charge to impart the electrical forces required for particle migration. It also permits the use of electrically conductive particles without regard to lateral conductivity of layer 11.
Reference is made to FIG. 7 showing the modification of the softenable layer by means of ultra-violet radiation. Illustratively, layer 12 of Staybelite 10 (2 microns in thickness) overlying aluminized Mylar substrate 13 is exposed for several minutes through image mask 21 to an image pattern of ultra-violet radiation from lamp 22.
Depending upon specific materials employed in the plate structure, other forms of actinic radiation may be used (either before or after formation of layer 11) to selectively modify the permeability of layer 12 to particle migration. Suitable methods include: X-ray treatment, Beta ray treatment, Gamma ray treatment and high energy electron bombardment.
As illustrated in FIG. 9, a substantially uniform electrostatic charge may be applied to layer 11 by moving corona discharge device 18 energized by high voltage power supply 19 in charging relation thereto. The corona device preferably applies a potential of at least about 20 volts to layer 11 with respect to substrate 13 to produce images of superior quality, especially as regards contrast. The instant process is operable, however, with much lower voltages, as the foregoing examples indicate. The charged plate may then be developed as described in connection with FIG. 4 and FIG. 5.
The foregoing description set forth for purposes of description and illustration is not intended to limit the invention as defined in the appended claims.
What is claimed is:
1. An imaging method comprising the steps of:
a. providing an imaging member comprising a fracturable layer contacting a solvent soluble layer overlying a substrate, said fracturable layer spaced apart from said substrate;
b. forming an electrostatic image on said member by imagewise depositing charge on said imaging member; and
c. applying a solvent for said solvent soluble layer to said member wherein said solvent is sufiiciently electrically insulating to prevent fracturable material from losing its charge before reaching said substrate and wherein said fracturable layer and said substrate are not entirely soluble in said solvent, whereby said solvent soluble layer and portions of said fracturable layer which are not charged are substantially removed and whereby portions of said fracturable layer which are charged are deposited on said substrate in image configuration.
2. An imaging method according to claim 1 wherein the electrostatic image is formed on said member by imagewise depositing corona discharge through an image cut stencil.
3. An imaging method according to claim 2 wherein said substrate is electrically conductive and is grounded at least during said stencil charging operation.
4. An imaging method according to claim 1 wherein the electrostatic image is formed on said imaging member by bringing an electrostatic image carrying member into electrical contact with said imaging member.
5. An imaging method according to claim 4 wherein said electrostatic image carrying member comprises a xerographic plate.
6. An imaging method according to claim 1 wherein the electrostatic image is formed on said imaging member by positioning a shaped electrode in close proximity to said member then pulsing said electrode with a high voltage.
7. An imaging method according to claim 1 wherein the electrostatic image is formed on said imaging member by writing on it with a low energy electron beam.
8. An imaging method according to claim 1 wherein said fracturable layer comprises predominantly particles and is between about 0.2 to about 10 microns thick.
Claims (7)
- 2. An imaging method according to claim 1 wherein the electrostatic image is formed on said member by imagewise depositing corona discharge through an image cut stencil.
- 3. An imaging method according to claim 2 wherein said substrate is electrically conductive and is grounded at least during said stencil charging operation.
- 4. An imaging method according to claim 1 wherein the electrostatic image is formed on said imaging member by bringing an electrostatic image carrying member into electrical contact with said imaging member.
- 5. An imaging method according to claim 4 wherein said electrostatic image carrying member comprises a xerographic Plate.
- 6. An imaging method according to claim 1 wherein the electrostatic image is formed on said imaging member by positioning a shaped electrode in close proximity to said member then pulsing said electrode with a high voltage.
- 7. An imaging method according to claim 1 wherein the electrostatic image is formed on said imaging member by writing on it with a low energy electron beam.
- 8. An imaging method according to claim 1 wherein said fracturable layer comprises predominantly particles and is between about 0.2 to about 10 microns thick.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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US40300264A | 1964-10-12 | 1964-10-12 | |
US42316765A | 1965-01-04 | 1965-01-04 | |
US46037765A | 1965-06-01 | 1965-06-01 | |
US48367565A | 1965-08-30 | 1965-08-30 |
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US460377A Expired - Lifetime US3520681A (en) | 1964-10-12 | 1965-06-01 | Photoelectrosolography |
US483675A Expired - Lifetime US3656990A (en) | 1964-10-12 | 1965-08-30 | Electrosolography |
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Application Number | Title | Priority Date | Filing Date |
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US460377A Expired - Lifetime US3520681A (en) | 1964-10-12 | 1965-06-01 | Photoelectrosolography |
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US (2) | US3520681A (en) |
CH (3) | CH509615A (en) |
DE (1) | DE1497219C3 (en) |
DK (1) | DK129303B (en) |
FR (1) | FR1466349A (en) |
GB (1) | GB1152365A (en) |
IL (1) | IL24435A (en) |
SE (1) | SE315804B (en) |
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US3839030A (en) * | 1967-06-01 | 1974-10-01 | Xerox Corp | Migration imaging process with uniform exposure before or during the softening step |
US3839031A (en) * | 1969-09-02 | 1974-10-01 | Xerox Corp | Electrode development migration imaging method |
USB327363I5 (en) * | 1973-01-29 | 1975-01-28 | ||
US3975195A (en) * | 1964-10-12 | 1976-08-17 | Xerox Corporation | Migration imaging system |
US3975739A (en) * | 1964-10-12 | 1976-08-17 | Xerox Corporation | Migration imaging system using shaped electrode |
US3976483A (en) * | 1970-01-02 | 1976-08-24 | Xerox Corporation | Erasing process |
US3985560A (en) * | 1969-08-21 | 1976-10-12 | Xerox Corporation | Migration imaging member with fusible particles |
US4012250A (en) * | 1970-01-02 | 1977-03-15 | Xerox Corporation | Imaging system |
US4072517A (en) * | 1975-04-29 | 1978-02-07 | Xerox Corporation | Migration imaging method |
US4081273A (en) * | 1970-01-02 | 1978-03-28 | Xerox Corporation | Migration imaging method |
US4101321A (en) * | 1967-01-27 | 1978-07-18 | Xerox Corporation | Imaging system |
US4157259A (en) * | 1974-03-25 | 1979-06-05 | Xerox Corporation | Erasure in migration imaging system |
US4281050A (en) * | 1966-07-21 | 1981-07-28 | Xerox Corporation | Migration imaging system |
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US3791822A (en) * | 1964-10-12 | 1974-02-12 | Xerox Corp | Removal of background from an imaged migration layer |
US3719482A (en) * | 1964-10-12 | 1973-03-06 | Xerox Corp | Imaging system |
US3982936A (en) * | 1966-01-13 | 1976-09-28 | Xerox Corporation | Deformation imaging system |
GB1200094A (en) * | 1966-10-31 | 1970-07-29 | Rank Xerox Ltd | Electrostatographic imaging method |
BE709131A (en) * | 1967-01-13 | 1968-07-09 | Rank Xerox Ltd | |
GB1204749A (en) * | 1967-10-17 | 1970-09-09 | Xerox Corp | Electrophotographic transfer process |
FR1587252A (en) * | 1967-11-01 | 1970-03-13 | ||
US3854943A (en) * | 1969-07-30 | 1974-12-17 | Xerox Corp | Manifold imaging method and member employing fundamental particles of alpha metal-free phthalocyanine |
US3720513A (en) * | 1969-08-21 | 1973-03-13 | Xerox Corp | Migration imaging method involving solvent wash-away of unmigrated particles |
US3648607A (en) * | 1969-08-21 | 1972-03-14 | Xerox Corp | Imaging system |
US3753706A (en) * | 1969-10-29 | 1973-08-21 | Xerox Corp | A photoelectrosolographic imaging method wherein an absorbent material is used |
US3901702A (en) * | 1969-10-29 | 1975-08-26 | Xerox Corp | Imaging element with absorbent blotter overlayer migration |
US3836364A (en) * | 1970-03-23 | 1974-09-17 | Xerox Corp | Method of making multiple images from a migration imaged member |
US3873309A (en) * | 1970-06-18 | 1975-03-25 | Xerox Corp | Imaging method using migration material |
US3894869A (en) * | 1970-06-18 | 1975-07-15 | Xerox Corp | Polychromatic migration imaging system |
US3912505A (en) * | 1972-08-16 | 1975-10-14 | Xerox Corp | Color imaging method employing a monolayer of beads |
US4168163A (en) * | 1975-05-08 | 1979-09-18 | Fuji Photo Film Co., Ltd. | Particle migration type sensitive materials and method of using the same |
US4278335A (en) * | 1980-01-25 | 1981-07-14 | Xerox Corporation | Camera with development and viewing means |
EP1033706B1 (en) | 1988-05-17 | 2004-03-03 | Dai Nippon Printing Co., Ltd. | Electrostatic information recording medium and electrostatic information recording and reproducing method |
US5731116A (en) * | 1989-05-17 | 1998-03-24 | Dai Nippon Printing Co., Ltd. | Electrostatic information recording medium and electrostatic information recording and reproducing method |
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US3975195A (en) * | 1964-10-12 | 1976-08-17 | Xerox Corporation | Migration imaging system |
US3975739A (en) * | 1964-10-12 | 1976-08-17 | Xerox Corporation | Migration imaging system using shaped electrode |
US4281050A (en) * | 1966-07-21 | 1981-07-28 | Xerox Corporation | Migration imaging system |
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US4072517A (en) * | 1975-04-29 | 1978-02-07 | Xerox Corporation | Migration imaging method |
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Also Published As
Publication number | Publication date |
---|---|
SE315804B (en) | 1969-10-06 |
CH493868A (en) | 1970-07-15 |
CH509615A (en) | 1971-06-30 |
GB1152365A (en) | 1969-05-14 |
CH1396065A4 (en) | 1970-11-13 |
DK129303B (en) | 1974-09-23 |
IL24435A (en) | 1969-12-31 |
DK129303C (en) | 1975-02-10 |
DE1497219B2 (en) | 1975-04-24 |
DE1497219A1 (en) | 1969-05-08 |
US3520681A (en) | 1970-07-14 |
DE1497219C3 (en) | 1975-12-18 |
FR1466349A (en) | 1967-01-20 |
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