US3717463A - Electrophotographic multicolor copy developed receptor employing solubilizable dyes - Google Patents
Electrophotographic multicolor copy developed receptor employing solubilizable dyes Download PDFInfo
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- US3717463A US3717463A US00157024A US3717463DA US3717463A US 3717463 A US3717463 A US 3717463A US 00157024 A US00157024 A US 00157024A US 3717463D A US3717463D A US 3717463DA US 3717463 A US3717463 A US 3717463A
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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
- G03G13/01—Electrographic processes using a charge pattern for multicoloured copies
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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
- G03G5/12—Recording members for multicolour processes
Definitions
- This invention relates to an electrophotographic process, materials and elements for the production of true color copies from multi-color originals with but a single exposure to light.
- FIG. 1 is a top plan view of a portion of a receptor embodying the coatings applied in accordance with a preferred practice of this invention
- FIG. 2 is an enlarged sectional view through a portion of the receptor sheet shown in FIG. 1;
- FIG. 3 is a schematic sectional view similar to that of FIG. 2, illustrating the conditions existing in response to exposure to a multi-color original;
- FIG. 4 is a schematic sectional view of the exposed receptor of FIG, 3 after treatment with a developer composition
- FIG. 5 is a schematic diagram showing the transfer of the multi-color image from the receptor to a copy sheet.
- FIG. 6 is a top plan view of the multi-color copy produced from the exposed receptor of FIG. 5.
- the concepts of this invention are practiced with a receptor provided with a number of photoconductive coatings each of which is formulated to contain (1) an organic insulating binder, such as an organo- Patented Feb. 20, 1973 silicon resin, a butadiene-styrene copolymer resin, a modified alkyd resin and the like; (2) a photoconductor such as photoconductive zinc oxide or other photoconductive material such as described in the Middleton et al. Pat. No.
- an organic insulating binder such as an organo- Patented Feb. 20, 1973 silicon resin, a butadiene-styrene copolymer resin, a modified alkyd resin and the like
- a photoconductor such as photoconductive zinc oxide or other photoconductive material such as described in the Middleton et al. Pat. No.
- a sensitizing component such as a sensitizing dye which sensitizes the photoconductor to light of a selected wave length within the visible light spectrum while reflecting wave lengths outside said range, with each coating containing a sensitizing ingredient which sensitizes the photoconductive coating to a dilferent portion of the visible light range, whereby the total of the coating provides sensitivity which covers the entire visible light range, and (4) a soluble dye component in each coating having a color transfer value corresponding to the subtractive color for which the particular coating is sensitized, as represented by a color produced by the combination of ranges of light reflected by the sensitized photoconductor of the particular coating composition and in which the concepts of this invention include the use of a developer which is formulated with a component, normally identified as a toner, which comprises a solid material in finely divided form which, in response to activation as by heat, solvent, vapors or the like, functions as a solvent for the soluble dye component (4) of the photoconductive coating to
- the visible spectrum may be subdivided into contiguous segments, preferably three or more segments, such as subdivision of the visible light spectrum, assumed to be included within the range of 400-700 am, into segments of about 400-500, 500-600 and 600-700 nm.
- the sensitizing component for one coating would then be selected to sensitize the photoconductor to light of within the range of 400-500 nm. (blue sensitivity) and to reflect light within the range of 500-700 nm.
- This particular effect can be achieved by the use of a dyestuff corresponding to the yellow layer in the well known photographic color processes based upon the subtractive tri-pack, such as Auramine 0 (Cl. 41,000).
- the soluble dye component formulated into the described coating composition is selected of a dyestutf having a yellow color or a color which represents the combination of the reflected light range of 500-700 nm.
- Another or second coating is formulated with a sensitizing component effective to sensitize the photoconductor in the light range of 500-600 nm. (green sensitivity), while reflecting light within the range of 400-500 nm. and 600-700 nm.
- a sensitizing component effective to sensitize the photoconductor in the light range of 500-600 nm. (green sensitivity), while reflecting light within the range of 400-500 nm. and 600-700 nm.
- This can be achieved by the use of a magenta coating, when reference is made to the subtracti ve tri-pack system, such as by formulating the coating composition to contain acridine red (C.l. 45,000).
- the soluble dye component formulated into the described coating would be selected of a dyestuff having preferably a blue-red color corresponding to the combination of the reflected light within the range of 400-500 and 600- 700 nm.
- the third coating would be formulated to contain a sensitizing component which sensitizes the photoconductor to absorbed light within the range of 600-700 nm. (red sensitivity), while reflecting light within the range of 400-600 nm. This can be achieved by a cyan coat, such as with Patent Blue (C.I. 42,045).
- the soluble dye component in the third coating would be selected of a dyestuff giving a blue-green color corresponding to the range of reflected light or the combination of colors within the range of 400-600 nm.
- the described coating compositions can be formulated to contain the resinous binder in an amount within the range of 10-40 parts by weight of resinous binder per 100 parts by weight of zinc oxide, and preferably in an amount within the range of 15-30 parts by weight of resinous binder per 100 parts by weight of zinc oxide.
- the sensitizing component or dyestuif is formulated in the coating composition in an amount within the range of 0.001 to 5.0 part by weight per 100 parts by weight zinc oxide and preferably within the range of 0.01 to 2.5 part by weight per 100 parts by weight of zinc oxide, the amount depending somewhat upon the sensitizing dye, such as 0.13% by weight magenta color, as in the form of acridine red having a spectral response in the range of 495-620 A., 0.06% of the cyan color, as represented by Patent Blue having a spectral response in the range of 600700 A. and 1.2% by weight of the yellow color as represented by Auramine having a spectral response within the range of 405-500 A.
- sensitizer per 100 parts by weight zinc oxide
- the soluble dye component can be formulated into each coating in an amount within the range of 0.5-20.0 parts by weight per 100 parts by weight of zinc oxide and preferably in an amount within the range of 1-5 parts by weight per 100 parts by weight of zinc oxide.
- sensitizer and soluble dye components specified in parts by weight may be taken as corresponding to the percent by weight of the photoconductive coatings formulated of photoconductive zinc oxide or a photoconductor other than zinc oxide, but in which the percentage is adjusted by the weight ratio of zinc oxide to said other photoconductive material in the coating.
- the soluble dye component is preferably formulated in the respective coating compositions as a dispersed dye but it will be understood that the soluble dye component can be incorporated in other states.
- the coatings are produced from compositions containing the described components in combination with a diluent which is a solvent for the resinous binder and ap plication may be made to the substrate in coating weights, when formulated of a zinc oxide photoconductor, within the range of 8-40 pounds per 3,000 square feet of surface area, and preferably within the range of -30 pounds per 3,000 square feet of surface area.
- the separate coating compositions are applied or otherwise imprinted on the surface of the substrate in various patterns.
- the essential requirement is that the face of the coated substrate define a final pattern of separate, small light responsive areas of each coating interspersed one with another substantially uniformly over the surface of the substrate in closely spaced relation.
- the separate coating compositions can be applied in a pattern of dots, circles, beads, spheres, squares, lines or the like configurations. Since it is not essential that the separate light responsive areas be arranged coplanar, it is preferred to apply the coating compositions either in the form of lines which criss-cross one another over the surface of the substrate or more preferably to apply one coating composition as a continuous coating over the surface of the substrate and to apply the remaining coatings as lines which criss-cross over the underlying base coat as islands or dots of various configuration which overlie the base coat.
- the receptor sheet will be formed of a substrate having portions coated with only one layer of the first coating, other portions with two layers formed of the first and second coats and first and third coats; and still other portions formed of three layers of the first, second and third coating, etc.
- the resinous binder, zinc oxide and solvent are first blended together by mixing for about five minutes.
- the sensitizing dye, in solution in methanol, is added and blended by mixing for about one minute.
- the dispersed dye is finally added and blended with mixing for about one to two minutes.
- the first coating 20, which may be the magenta coat of Example 1, is applied either by a roller coater, by a metering rod, or by hand draw-down a wire wound rod, onto Weyerhauser Base A paper 10 in a coating weight of about 20 pounds per 3,000 square feet, and then dried.
- the yellow coating composition of Example 2 is applied, as by silk screen, in a coating weight of about 15 pounds per 3,000 square feet of surface area in a pattern of closely spaced parallel lines 22 which extend crosswise over the surface of the first coating 20.
- coatings can be applied in various other sequences such as a first coating of the yellow coat of Example 2 followed by second and third coatings of Examples 1 and 3, or a first coat of Example 3 and second and third coatings of Examples 3 and 2 or 2 and 3, etc.
- the cyan coating composition of Example 3 is also applied, as by silk screen, in a coating weight of about 15 pounds per 3,000 square feet of surface area in a pattern of closely spaced parallel lines 24 which extend lengthwise over the first and second coatings to provide cross-over points 26 having three thicknesses of coating with the third coating 24 uppermost on the face of the substrate or paper base sheet.
- the final coated sheet constitutes a receptor suitable for use in the practice of this invention with separate sections 28 having a single coating thickness of the magenta coating, separate sections 3 having a double coating thickness formed of a lowermost magenta coating 20 and an uppermost yellow coating 22 and a lowermost magenta coating 20 and an uppermost cyan coating 24 and still other sections 32 having a triple coating thickness formed of a lowermost magenta coating 20, an intermediate yello-w coating 22 and an uppermost cyan coating 24.
- the exposed face of the receptor presents separate sections of each of the coatings in substantially uniformly dispersed relation over the face of the receptor sheet.
- the receptor sheet is charged in the usual manner, now well known to the electrostatic copy art, as by subjecting the face of the receptor to a corona spray as it is exposed to corona discharge from wires operating at a potential of about 6000 to 8000 volts.
- the charged wires which extend across the face of the receptor, are either transported over the face of the receptor or the receptor is displaced beneath the wires.
- the electrostatic charge is deposited over the entire receptor covered by one or more of the photoconductive coatings.
- the charged receptor is next exposed to the multicolor original.
- Such portions of the original which are blue in color, for example, will cause discharge of the corresponding areas on the face of the receptor formed of the yellow coating which is sensitized to blue, leaving the charges in the corresponding areas on the exposed face sections of the magenta and cyan coatings for subsequent development.
- the portions of the original which are green in color cause discharge of the corresponding areas 28 on the face of the receptor formed of the magenta coating, which are sensitized to green, leaving the charge 34 on the corresponding areas on the face sections 32 of cyan and sections 30 of yellow coating for subsequent development, as depicted in FIG. 3.
- the portions of the original which have the color red will cause discharge in the corresponding areas of the receptor of the cyan sections 32 on the exposed face of the receptor sheet which are sensitized to red, leaving the charges on the corresponding areas in the exposed face sections of magenta and yellow for subsequent development.
- the exposed receptor sheet is developed in the conventional manner either with a dry powder developer or with a liquid developer, but in which the conventional particles of toner in the dry powder developer suspended in the liquid developer are substituted by finely divided particles of a compound which, when activated as by heat or solvent, vapor and the like, becomes a solvent for the dispersed dye in the coating.
- EXAMPLE 4 5.0 grams toner (Antipyrine) 400 ml. liquid carrier (Isopar GHumble Oil Co.) 5 grams charge director (Fuel Oil Additive #2DuPont)
- EXAMPLE 5 5.0 grams toner (l-allyl-Z-thiourea) 400 ml. liquid carrier 5 grams charge director
- the Isopar G used as the liquid carrier in the above example is a paraffinic hydrocarbon liquid having 11.8% C hydrocarbons, 56.2% C hydrocarbons, 31.7% C hydrocarbons, less than .3 aromatics and less than .1 olefins, a boiling point within the range of 3l8350 F., a flash point of 104 F. and a specific gravity of 0.748.
- the Fuel Oil Additive #2 is a solution of a methacrylate copolymer having an average molecular weight of 50,000. Again, other conventional charge directors can be employed.
- the antipyrine of Example 4 and the l-allyl-Z-thiourea 6 of Example 5 are merely representative of suitable toner particles which may be used for development of the latent electrostatic image of the charged sections that remain after exposure.
- suitable toner particles may be used which meet the requirements:
- a solvent for the soluble dye component in the coatings when the toner is in a molten or activated state capable of being reduced to a finely divided form in which it is retained in the liquid or powdered developer composition
- toner particles can be employed in various concentrations in the developer composition, such as within the range of 2-20% by weight, and preferably 3-l0% by weight, in a dry powder developer and within the range of 0.220% by weight and preferably 2-10% by weight in a liquid developer.
- the toner concentration can range up to percent by weight toner in the developer.
- toner particles 36 will be retained on the portions on the face of the receptor which remain charged to define the latent electrostatic image after exposure while the discharge sections on the face of the receptor will remain substantially free of the toner particles, as depicted in FIG. 4.
- the developer receptor sheet is pressed into surface contact with a copy sheet 40, as by passage of the composite assembly between compression rollers heated to a temperature above the melting point tem-- perature for the toner, such as at a temperature above 1l1l13 C. which is the melting point for antipyrine, or above a temperature of 7778 C. which is the melting point for 1-allyl-2-thiourea, and preferably by heating the toner particles to a temperature which exceeds their melting point by a slight amount preferably about 5-10 F.
- the toner particles are reduced to a fluidized state to enable solution of the dispersed dye in the underlying portions of the photoconductive coating in the face of the receptor for transfer of the corresponding dye color, as by diffusion, from the receptor to the copy sheet 40.
- the cyan and yellow coatings 32 and 30, respectively which remain charged and retain the toner particles 34 on development, solubilize the Calcofast Spirit Yellow TG and the Spirit Soluble Fast Blue 6G to cause transfer to the copy sheet with resultant reproduction 50 of the green color of the original.
- areas of the original which are black such as the printed areas, none of the sections in the face of the coated receptor would become discharged upon exposure.
- each of the areas accept toner for transfer of dyestuffs from all of the three basic color sections which together appear black in the copy sheet.
- the copy produced by the combination of colors transferred from the developed receptor sheet will correspond to the colored original and that the developed receptor can function in a manner of a spirit master to produce multiple copies of the multi-color original, as by the successive passage of copy sheets into pressure contact with the developed receptor until the soluble dyestutf in the toned face segments are exhausted.
- a developed receptor for electrophotographic production of multi-color copies of a multi-color original comprising a conductive substrate in the form of a sheet and two or more photoconductive sections interspersed on the face of the substrate, each section containing a photoconductive component and each different section containing a sensitizing component for sensitizing the photoconductor to a segment of the visible light range for absorption of light within said range and reflection of light outside said range, and a dye color component which corresponds to the color of the reflected range of light, with the sensitizing component in one section dilfering from the sensitizing component in other sections to cover substantially the entire visible light range, and toner particles electrostatically attracted to sections of the receptor which have retained a latent electrostatic image in response to exposure to an original whereby the toner particles are attracted to sections of the receptor in areas of the receptor corresponding to areas of the original having the same color as the dye color component of the sections, said toner particles being formed of a material which, when in activated state, serves as a solvent for the dye
- a receptor sheet as claimed in claim 1 in which the golor dye correspoding to the reflected light is a dispersed 6.
- a receptor sheet as claimed in claim 5 in which the soluble dye component is present in an amount within the range of 0.5 to 20 percent by weight per parts by weight of the photoconductive component when that photoconductive component is zinc oxide.
- a receptor sheet as claimed in claim 1 in which the separate sections are selected of three difierent compositions with each of the compositions containing a separate member of the subtractive tri-pack colors of magenta, cyan and yellow.
- a receptor sheet as claimed in claim 1 in which the sections are formed in a pattern of criss crossing lines of the diflerent compositions.
- a receptor sheet as claimed in claim 1 in which the sections on the substrate comprise a coating of one composition extending over the surface of the substrate with the other compositions arranged in criss-cross pattern of lines over the surface of the coating.
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Abstract
FOG-01 AN ELECTROPHOTOGRAPHIC PROCESS AND MATERIALS FOR THE PRODUCTION OF MULTI-COLOR COPIES OF A MULTI-COLOR ORGINAL IN WHICH AN ELECTROSTATIC CHARGE IS APPLIED TO A RECEPTOR SHEET HAVING A FACE PORTION SUBDIVIDED INTO PHOTOCONDUCTIVE SEGMENTS CONTAINING SENSITIZING COMPONENTS IN INTERSPERSED SEGMENTS WHICH COVER DIFFERENT PORTIONS OF THE VISIBLE LIGHT SPECTRUM AND IN WHICH EACH SUCH SEGMENT CONTAINS A SOLUBILIZABLE DYE COLOR CORRESPONDING TO THE COLOR OF THE SPECTRUM OTHER THAN THAT TO WHICH THE SEGMENT IS SENSITIZED AND IN WHICH THE EXPOSED RECEPTOR IS DEVELOPED WITH A TONER IN WHICH THE DYE COMPONENT IS SOLUBLE IN RESPONSE TO TONER ACTIVATION FOR TRANSFER OF DYE COLOR FROM THE DEVELOPED RECEPTOR TO COPY SHEETS BROUGHT INTO SURFACE CONTACT THEREWITH.
Description
Feb. 20, 1973 F. 0. EACH ETAL ELECTROPHOTOGRAPHIC MULTIGOLOR COPY DEVELOPED RECEPTOR EMPLOYING SOLUBILIZABLE DYES Original Filed June 25, 1969 FIG. Z
FIG, 4
Fire: 5
FIG. 6
United States Patent U.S. Cl. 96-15 11 Claims ABSTRACT OF THE DISCLOSURE An electrophotographic process and materials for the production of multi-color copies of a multi-color original in which an electrostatic charge is applied to a receptor sheet having a face portion subdivided into photoconductive segments containing sensitizing components in interspersed segments which cover diiferent portions of the visible light spectrum and in which each such segment contains a solubilizable dye color corresponding to the color of the spectrum other than that to which the segment is sensitized and in which the exposed receptor is developed with a toner in which the dye component is soluble in response to toner activation for transfer of dye color from the developed receptor to copy sheets brought into surface contact therewith.
This is a division of U.S. application Ser. No. 836,415, filed June 25, 1969, now U.S. Pat. No. 3,630,729.
This invention relates to an electrophotographic process, materials and elements for the production of true color copies from multi-color originals with but a single exposure to light.
It is an object of this invention to provide a process for producing true color copies of multi-color originals by use of an electrophotographic technique which requires but a single exposure to light; which makes use of a single receptor sheet from which one or a number of multicolor copies can be produced; in which the multi-color copy is produced by transfer from the receptor sheet to copy sheets for true color reproductions, and it is a related object to provide a composition and elements for use in the practice of same.
These and other objects and advantages of this invention will hereinafter appear and for purposes of illustration, but not of limitation, an embodiment of the invention is illustrated in the accompanying drawings in which:
FIG. 1 is a top plan view of a portion of a receptor embodying the coatings applied in accordance with a preferred practice of this invention;
FIG. 2 is an enlarged sectional view through a portion of the receptor sheet shown in FIG. 1;
FIG. 3 is a schematic sectional view similar to that of FIG. 2, illustrating the conditions existing in response to exposure to a multi-color original;
FIG. 4 is a schematic sectional view of the exposed receptor of FIG, 3 after treatment with a developer composition;
FIG. 5 is a schematic diagram showing the transfer of the multi-color image from the receptor to a copy sheet; and
FIG. 6 is a top plan view of the multi-color copy produced from the exposed receptor of FIG. 5.
Briefly described, the concepts of this invention are practiced with a receptor provided with a number of photoconductive coatings each of which is formulated to contain (1) an organic insulating binder, such as an organo- Patented Feb. 20, 1973 silicon resin, a butadiene-styrene copolymer resin, a modified alkyd resin and the like; (2) a photoconductor such as photoconductive zinc oxide or other photoconductive material such as described in the Middleton et al. Pat. No. 3,121,006; (3) a sensitizing component, such as a sensitizing dye which sensitizes the photoconductor to light of a selected wave length within the visible light spectrum while reflecting wave lengths outside said range, with each coating containing a sensitizing ingredient which sensitizes the photoconductive coating to a dilferent portion of the visible light range, whereby the total of the coating provides sensitivity which covers the entire visible light range, and (4) a soluble dye component in each coating having a color transfer value corresponding to the subtractive color for which the particular coating is sensitized, as represented by a color produced by the combination of ranges of light reflected by the sensitized photoconductor of the particular coating composition and in which the concepts of this invention include the use of a developer which is formulated with a component, normally identified as a toner, which comprises a solid material in finely divided form which, in response to activation as by heat, solvent, vapors or the like, functions as a solvent for the soluble dye component (4) of the photoconductive coating to effect transfer of the dye color from the portions of the coating immediately underlying the activated solvent for transfer to copy sheets pressed into surface contact with the receptor to produce true color copies of multi-color originals in response to a single exposure.
By way of illustration, the visible spectrum may be subdivided into contiguous segments, preferably three or more segments, such as subdivision of the visible light spectrum, assumed to be included within the range of 400-700 am, into segments of about 400-500, 500-600 and 600-700 nm. The sensitizing component for one coating would then be selected to sensitize the photoconductor to light of within the range of 400-500 nm. (blue sensitivity) and to reflect light within the range of 500-700 nm. This particular effect can be achieved by the use of a dyestuff corresponding to the yellow layer in the well known photographic color processes based upon the subtractive tri-pack, such as Auramine 0 (Cl. 41,000). The soluble dye component formulated into the described coating composition is selected of a dyestutf having a yellow color or a color which represents the combination of the reflected light range of 500-700 nm.
Another or second coating is formulated with a sensitizing component effective to sensitize the photoconductor in the light range of 500-600 nm. (green sensitivity), while reflecting light within the range of 400-500 nm. and 600-700 nm. This can be achieved by the use of a magenta coating, when reference is made to the subtracti ve tri-pack system, such as by formulating the coating composition to contain acridine red (C.l. 45,000). The soluble dye component formulated into the described coating would be selected of a dyestuff having preferably a blue-red color corresponding to the combination of the reflected light within the range of 400-500 and 600- 700 nm.
The third coating would be formulated to contain a sensitizing component which sensitizes the photoconductor to absorbed light within the range of 600-700 nm. (red sensitivity), while reflecting light within the range of 400-600 nm. This can be achieved by a cyan coat, such as with Patent Blue (C.I. 42,045). The soluble dye component in the third coating would be selected of a dyestuff giving a blue-green color corresponding to the range of reflected light or the combination of colors within the range of 400-600 nm.
When based upon the amount of photoconductive zinc oxide, the described coating compositions can be formulated to contain the resinous binder in an amount within the range of 10-40 parts by weight of resinous binder per 100 parts by weight of zinc oxide, and preferably in an amount within the range of 15-30 parts by weight of resinous binder per 100 parts by weight of zinc oxide. The sensitizing component or dyestuif is formulated in the coating composition in an amount within the range of 0.001 to 5.0 part by weight per 100 parts by weight zinc oxide and preferably within the range of 0.01 to 2.5 part by weight per 100 parts by weight of zinc oxide, the amount depending somewhat upon the sensitizing dye, such as 0.13% by weight magenta color, as in the form of acridine red having a spectral response in the range of 495-620 A., 0.06% of the cyan color, as represented by Patent Blue having a spectral response in the range of 600700 A. and 1.2% by weight of the yellow color as represented by Auramine having a spectral response within the range of 405-500 A. It will be understood that, except for cost, more than .0 parts by weight of sensitizer per 100 parts by weight zinc oxide can be used. The soluble dye component can be formulated into each coating in an amount within the range of 0.5-20.0 parts by weight per 100 parts by weight of zinc oxide and preferably in an amount within the range of 1-5 parts by weight per 100 parts by weight of zinc oxide. The foregoing amounts of sensitizer and soluble dye components specified in parts by weight may be taken as corresponding to the percent by weight of the photoconductive coatings formulated of photoconductive zinc oxide or a photoconductor other than zinc oxide, but in which the percentage is adjusted by the weight ratio of zinc oxide to said other photoconductive material in the coating.
The soluble dye component is preferably formulated in the respective coating compositions as a dispersed dye but it will be understood that the soluble dye component can be incorporated in other states.
The coatings are produced from compositions containing the described components in combination with a diluent which is a solvent for the resinous binder and ap plication may be made to the substrate in coating weights, when formulated of a zinc oxide photoconductor, within the range of 8-40 pounds per 3,000 square feet of surface area, and preferably within the range of -30 pounds per 3,000 square feet of surface area.
The separate coating compositions are applied or otherwise imprinted on the surface of the substrate in various patterns. The essential requirement is that the face of the coated substrate define a final pattern of separate, small light responsive areas of each coating interspersed one with another substantially uniformly over the surface of the substrate in closely spaced relation.
This can be accomplished by application of the separate coating compositions in a pattern of dots, circles, beads, spheres, squares, lines or the like configurations. Since it is not essential that the separate light responsive areas be arranged coplanar, it is preferred to apply the coating compositions either in the form of lines which criss-cross one another over the surface of the substrate or more preferably to apply one coating composition as a continuous coating over the surface of the substrate and to apply the remaining coatings as lines which criss-cross over the underlying base coat as islands or dots of various configuration which overlie the base coat. Thus the receptor sheet will be formed of a substrate having portions coated with only one layer of the first coating, other portions with two layers formed of the first and second coats and first and third coats; and still other portions formed of three layers of the first, second and third coating, etc.
Having described the basic concepts of the invention from the standpoint of compositions and construction of the elements employed, illustration will now be made by way of examples which represent the practice of the invention and in the utilization thereof in carrying out the new and novel process for multi-color reproduction of multi-color originals by the electrophotographic technique. The description will hereinafter be made with respect to a system of compositions based upon the substractive tripack, but it will be understood that the visible light spectrum can be otherwise divided for the selection of component identified as the sensitizing component and corresponding soluble dye component embodied in each of the separate coating formulations.
EXAMPLE 1 Magenta coating composition: (green sensitive):
100 grams photoconductive zinc oxide (Photox New Jersey Zinc Company) 25 grams modified alkyd resin (DeSoto E-l04-13A DeSoto Chemical Coatings, Inc.)
0.13 gram sensitizing dyeAcridine RedC.I. 45,000
(Allied Chemical Corp.)
1.5 grams dispersed dyespirit soluble Fast Red 33 (Allied Chemical Corp.)
60 ml. toluene EXAMPLE 2 Yellow coating composition (blue sensitive):
grams photoconductive zinc oxide (Photox 80) 25 grams modified alkyd resin (DeSoto E-104-13A) 0.05 gram sensitizing dyeAuramine OC.I. 41,000
(Allied Chemical Corp.)
1.5 grams dispersed dyeCalcofast Spirit Yellow TG (American Cyanamid Company) 60 ml. solvent-toluene EXAMPLE 3 Cyan coating composition (red sensitive):
100 grams photoconductive zinc oxide (Photox 80) 25 grams modified alkyd resin (DeSoto E-104-13A) 0.05 gram sensitizing dyePateut BlueC.I. 42,045
(Allied Chemical Corp.)
1.5 grams dispersed dyespirit soluble Fast Blue 66 (Allied Chemical Corp.)
60 ml. solvent-toluene In each of the examples, the resinous binder, zinc oxide and solvent are first blended together by mixing for about five minutes. The sensitizing dye, in solution in methanol, is added and blended by mixing for about one minute. The dispersed dye is finally added and blended with mixing for about one to two minutes.
The first coating 20, which may be the magenta coat of Example 1, is applied either by a roller coater, by a metering rod, or by hand draw-down a wire wound rod, onto Weyerhauser Base A paper 10 in a coating weight of about 20 pounds per 3,000 square feet, and then dried. The yellow coating composition of Example 2 is applied, as by silk screen, in a coating weight of about 15 pounds per 3,000 square feet of surface area in a pattern of closely spaced parallel lines 22 which extend crosswise over the surface of the first coating 20. It will be understood that the described coatings can be applied in various other sequences such as a first coating of the yellow coat of Example 2 followed by second and third coatings of Examples 1 and 3, or a first coat of Example 3 and second and third coatings of Examples 3 and 2 or 2 and 3, etc.
The cyan coating composition of Example 3 is also applied, as by silk screen, in a coating weight of about 15 pounds per 3,000 square feet of surface area in a pattern of closely spaced parallel lines 24 which extend lengthwise over the first and second coatings to provide cross-over points 26 having three thicknesses of coating with the third coating 24 uppermost on the face of the substrate or paper base sheet.
The final coated sheet constitutes a receptor suitable for use in the practice of this invention with separate sections 28 having a single coating thickness of the magenta coating, separate sections 3 having a double coating thickness formed of a lowermost magenta coating 20 and an uppermost yellow coating 22 and a lowermost magenta coating 20 and an uppermost cyan coating 24 and still other sections 32 having a triple coating thickness formed of a lowermost magenta coating 20, an intermediate yello-w coating 22 and an uppermost cyan coating 24. Thus the exposed face of the receptor presents separate sections of each of the coatings in substantially uniformly dispersed relation over the face of the receptor sheet.
The receptor sheet is charged in the usual manner, now well known to the electrostatic copy art, as by subjecting the face of the receptor to a corona spray as it is exposed to corona discharge from wires operating at a potential of about 6000 to 8000 volts. The charged wires, which extend across the face of the receptor, are either transported over the face of the receptor or the receptor is displaced beneath the wires. The electrostatic charge is deposited over the entire receptor covered by one or more of the photoconductive coatings.
The charged receptor is next exposed to the multicolor original. Such portions of the original which are blue in color, for example, will cause discharge of the corresponding areas on the face of the receptor formed of the yellow coating which is sensitized to blue, leaving the charges in the corresponding areas on the exposed face sections of the magenta and cyan coatings for subsequent development.
The portions of the original which are green in color cause discharge of the corresponding areas 28 on the face of the receptor formed of the magenta coating, which are sensitized to green, leaving the charge 34 on the corresponding areas on the face sections 32 of cyan and sections 30 of yellow coating for subsequent development, as depicted in FIG. 3.
Similarly, the portions of the original which have the color red will cause discharge in the corresponding areas of the receptor of the cyan sections 32 on the exposed face of the receptor sheet which are sensitized to red, leaving the charges on the corresponding areas in the exposed face sections of magenta and yellow for subsequent development.
The exposed receptor sheet is developed in the conventional manner either with a dry powder developer or with a liquid developer, but in which the conventional particles of toner in the dry powder developer suspended in the liquid developer are substituted by finely divided particles of a compound which, when activated as by heat or solvent, vapor and the like, becomes a solvent for the dispersed dye in the coating.
The following examples are given by way of illustration, but not by way of limitation, of liquid developing compositions embodying the features of this invention.
EXAMPLE 4 5.0 grams toner (Antipyrine) 400 ml. liquid carrier (Isopar GHumble Oil Co.) 5 grams charge director (Fuel Oil Additive #2DuPont) EXAMPLE 5 5.0 grams toner (l-allyl-Z-thiourea) 400 ml. liquid carrier 5 grams charge director The Isopar G used as the liquid carrier in the above example is a paraffinic hydrocarbon liquid having 11.8% C hydrocarbons, 56.2% C hydrocarbons, 31.7% C hydrocarbons, less than .3 aromatics and less than .1 olefins, a boiling point within the range of 3l8350 F., a flash point of 104 F. and a specific gravity of 0.748. Other liquid carriers used in liquid developers may be used as long as the toner compound is not dissolved therein. The Fuel Oil Additive #2 is a solution of a methacrylate copolymer having an average molecular weight of 50,000. Again, other conventional charge directors can be employed.
The antipyrine of Example 4 and the l-allyl-Z-thiourea 6 of Example 5 are merely representative of suitable toner particles which may be used for development of the latent electrostatic image of the charged sections that remain after exposure. Other toner particles may be used which meet the requirements:
(1) a solvent for the soluble dye component in the coatings when the toner is in a molten or activated state; (2) capable of being reduced to a finely divided form in which it is retained in the liquid or powdered developer composition;
(3) capable of taking on a charge, such as a positive charge when used with a charged photoconductive coating of zinc oxide;
(4) suitably located within the triboelectric series to produce the desirable charge development.
Representative of other suitable compounds which meet these requirements and can be used as toners are vanillin. 1,6-hexanediol, 1,10-decanediol, ethyl urea, acetamide, benzohydrol, 2,2-dimethyl-l, 3-propanediol, ammonium acetate, ammonium formate and pyrazine. The toner particles can be employed in various concentrations in the developer composition, such as within the range of 2-20% by weight, and preferably 3-l0% by weight, in a dry powder developer and within the range of 0.220% by weight and preferably 2-10% by weight in a liquid developer. When use is made of a dry powdered developer which is applied by brushing or the like, the toner concentration can range up to percent by weight toner in the developer.
Continuing with the development process, in response to the application of the developer composition, toner particles 36 will be retained on the portions on the face of the receptor which remain charged to define the latent electrostatic image after exposure while the discharge sections on the face of the receptor will remain substantially free of the toner particles, as depicted in FIG. 4.
Thereafter the developer receptor sheet is pressed into surface contact with a copy sheet 40, as by passage of the composite assembly between compression rollers heated to a temperature above the melting point tem-- perature for the toner, such as at a temperature above 1l1l13 C. which is the melting point for antipyrine, or above a temperature of 7778 C. which is the melting point for 1-allyl-2-thiourea, and preferably by heating the toner particles to a temperature which exceeds their melting point by a slight amount preferably about 5-10 F. As a result, the toner particles are reduced to a fluidized state to enable solution of the dispersed dye in the underlying portions of the photoconductive coating in the face of the receptor for transfer of the corresponding dye color, as by diffusion, from the receptor to the copy sheet 40.
In the example illustrated in FIGS. 4 and 5, the cyan and yellow coatings 32 and 30, respectively, which remain charged and retain the toner particles 34 on development, solubilize the Calcofast Spirit Yellow TG and the Spirit Soluble Fast Blue 6G to cause transfer to the copy sheet with resultant reproduction 50 of the green color of the original. In such areas of the original which are black, such as the printed areas, none of the sections in the face of the coated receptor would become discharged upon exposure. As a result, each of the areas accept toner for transfer of dyestuffs from all of the three basic color sections which together appear black in the copy sheet.
It will be apparent that the copy produced by the combination of colors transferred from the developed receptor sheet will correspond to the colored original and that the developed receptor can function in a manner of a spirit master to produce multiple copies of the multi-color original, as by the successive passage of copy sheets into pressure contact with the developed receptor until the soluble dyestutf in the toned face segments are exhausted.
It will be apparent from the foregoing that I have provided a new and novel electrophotographic process for the production of true color copies of multi-color originals by the use of but a single exposure for the development of a master from which one or more multi-colored copies can be produced.
It will be understood that changes may be made in the details of formulations, application and process steps, without departing from the spirit of the invention, especially as defined in the following claims.
We claim:
1. A developed receptor for electrophotographic production of multi-color copies of a multi-color original comprising a conductive substrate in the form of a sheet and two or more photoconductive sections interspersed on the face of the substrate, each section containing a photoconductive component and each different section containing a sensitizing component for sensitizing the photoconductor to a segment of the visible light range for absorption of light within said range and reflection of light outside said range, and a dye color component which corresponds to the color of the reflected range of light, with the sensitizing component in one section dilfering from the sensitizing component in other sections to cover substantially the entire visible light range, and toner particles electrostatically attracted to sections of the receptor which have retained a latent electrostatic image in response to exposure to an original whereby the toner particles are attracted to sections of the receptor in areas of the receptor corresponding to areas of the original having the same color as the dye color component of the sections, said toner particles being formed of a material which, when in activated state, serves as a solvent for the dye color component.
2. A receptor sheet as claimed in claim 1 in which the photoconductive component comprises photoconductive zinc oxide.
3. A receptor sheet as claimed in claim 1 in which the sensitizing component is a sensitizing dye.
4. A receptor sheet as claimed in claim 3 in which the sensitizing dye is present in an amount within the range of 0.001 to 5.0 percent by weight per 100 parts by weight of the photoconductive component when that photoconductive component is zinc oxide.
5. A receptor sheet as claimed in claim 1 in which the golor dye correspoding to the reflected light is a dispersed 6. A receptor sheet as claimed in claim 5 in which the dispersed dye is a spirit soluble dye.
7. A receptor sheet as claimed in claim 5 in which the soluble dye component is present in an amount within the range of 0.5 to 20 percent by weight per parts by weight of the photoconductive component when that photoconductive component is zinc oxide.
8. A receptor sheet as claimed in claim 1 in which the separate sections are selected of three difierent compositions with each of the compositions containing a separate member of the subtractive tri-pack colors of magenta, cyan and yellow.
9. A receptor sheet as claimed in claim 1 in which the sections are formed in a pattern of criss crossing lines of the diflerent compositions.
10. A receptor sheet as claimed in claim 1 in which the sections are formed of a pattern of separate islands of the different compositions.
11. A receptor sheet as claimed in claim 1 in which the sections on the substrate comprise a coating of one composition extending over the surface of the substrate with the other compositions arranged in criss-cross pattern of lines over the surface of the coating.
References Cited UNITED STATES PATENTS 3,212,887 10/1965 Miller et al 961.2 X 3,329,590 7/1967 Renfrow 961.2 X 2,940,847 6/1960 Kaprelian 96l.2 X 3,147,699 9/ 1964 Land 96l.2 X 2,962,374 11/1960 Dessauer 961.2 X 3,549,359 12/1970 Honjo et al. 961.2 3,556,783 1/ 1971 Kyriakakis 96l.2
GEORGE F. LESMES, Primary Examiner J. R. MILLER, Assistant Examiner U.S. C1. X.R.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US15702471A | 1971-06-25 | 1971-06-25 |
Publications (1)
Publication Number | Publication Date |
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US3717463A true US3717463A (en) | 1973-02-20 |
Family
ID=22562065
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US00157024A Expired - Lifetime US3717463A (en) | 1971-06-25 | 1971-06-25 | Electrophotographic multicolor copy developed receptor employing solubilizable dyes |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3879196A (en) * | 1971-11-15 | 1975-04-22 | Canon Kk | Electrophotographic method for colored images |
US3880656A (en) * | 1971-10-02 | 1975-04-29 | Canon Kk | Electrophotographic method for colored images |
US4040828A (en) * | 1975-01-06 | 1977-08-09 | Xerox Corporation | Multicolor imaging method and imaged member employing combinations of transparent toner and colorant |
FR2550036A1 (en) * | 1983-07-30 | 1985-02-01 | Sony Corp | METHOD FOR FORMING A COLOR IMAGE |
US4911999A (en) * | 1988-12-13 | 1990-03-27 | E. I. Du Pont De Nemours And Company | Electrostatic master containing thiourea or thioamide electrostatic decay additive for high speed xeroprinting |
-
1971
- 1971-06-25 US US00157024A patent/US3717463A/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3880656A (en) * | 1971-10-02 | 1975-04-29 | Canon Kk | Electrophotographic method for colored images |
US3879196A (en) * | 1971-11-15 | 1975-04-22 | Canon Kk | Electrophotographic method for colored images |
US4040828A (en) * | 1975-01-06 | 1977-08-09 | Xerox Corporation | Multicolor imaging method and imaged member employing combinations of transparent toner and colorant |
FR2550036A1 (en) * | 1983-07-30 | 1985-02-01 | Sony Corp | METHOD FOR FORMING A COLOR IMAGE |
US4911999A (en) * | 1988-12-13 | 1990-03-27 | E. I. Du Pont De Nemours And Company | Electrostatic master containing thiourea or thioamide electrostatic decay additive for high speed xeroprinting |
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