US3401037A - Electrostatic printing on metal substrates - Google Patents

Electrostatic printing on metal substrates Download PDF

Info

Publication number
US3401037A
US3401037A US414024A US41402464A US3401037A US 3401037 A US3401037 A US 3401037A US 414024 A US414024 A US 414024A US 41402464 A US41402464 A US 41402464A US 3401037 A US3401037 A US 3401037A
Authority
US
United States
Prior art keywords
coating
image
printing
metal substrates
electrostatic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US414024A
Inventor
Roteman Jerome
Sebastian T Brancato
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Interchemical Corp
Original Assignee
Interchemical Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Interchemical Corp filed Critical Interchemical Corp
Priority to US414024A priority Critical patent/US3401037A/en
Application granted granted Critical
Publication of US3401037A publication Critical patent/US3401037A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—Charge-receiving layers
    • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/05—Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
    • G03G5/0528—Macromolecular bonding materials
    • G03G5/0557—Macromolecular bonding materials obtained otherwise than by reactions only involving carbon-to-carbon unsatured bonds
    • G03G5/0567—Other polycondensates comprising oxygen atoms in the main chain; Phenol resins
    • 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
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—Charge-receiving layers
    • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/05—Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
    • G03G5/0528—Macromolecular bonding materials
    • G03G5/0532—Macromolecular bonding materials obtained by reactions only involving carbon-to-carbon unsatured bonds
    • G03G5/0546—Polymers comprising at least one carboxyl radical, e.g. polyacrylic acid, polycrotonic acid, polymaleic acid; Derivatives thereof, e.g. their esters, salts, anhydrides, nitriles, amides
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—Charge-receiving layers
    • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/05—Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
    • G03G5/0528—Macromolecular bonding materials
    • G03G5/0557—Macromolecular bonding materials obtained otherwise than by reactions only involving carbon-to-carbon unsatured bonds
    • G03G5/056—Polyesters
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—Charge-receiving layers
    • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/05—Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
    • G03G5/0528—Macromolecular bonding materials
    • G03G5/0557—Macromolecular bonding materials obtained otherwise than by reactions only involving carbon-to-carbon unsatured bonds
    • G03G5/0575—Other polycondensates comprising nitrogen atoms with or without oxygen atoms in the main chain
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00—Developers
    • G03G9/08—Developers with toner particles
    • G03G9/12—Developers with toner particles in liquid developer mixtures

Definitions

  • This invention relates to electrostatic printing and particularly to electrostatic printing on metal substrates.
  • An electrostatic printing process is a process for producing a visibile image or copy by converting a light image or signal into an electrostatic charge pattern on an electrically insulating base. The charge pattern is then converted or developed into a visible image by the application thereto of electrically-attractable particles.
  • a typical electrostatic printing process utilizing a photoconducting insulating stratum includes first producing a blanket electrostatic charge on the surface of the photoconducting stratum. The electrostatic charge may be stored on th surface for a time in the dark. Within the period in which a substantial charge remains, a light image is focused on the charged surface, discharging the portions of the surface irradiated with light, leaving the remainder of the surface in a charged condition, and thereby forming an electrostatic image thereon.
  • the electrostatic image is rendered visible by applying to the electrostatic image a developer substance, such as a pigmented thermoplastic resin powder, which is held electrostatically to the charged areas of the surface.
  • a developer substance such as a pigmented thermoplastic resin powder
  • the visible image thus formed may be fixed directly to the surface, for example, by fusing the image thereto.
  • thermoplastic resin powder A process of electrostatic printing in which the thermoplastic resin powder is fused directly to the surface of the stratum is described in US. Patents 3,052,539 and 3,052,540, both to H. G. Greig.
  • thermosetting binders have been considered in place of the thermoplastic binders. However, these thermosetting binders have always been heated to effect'at leasta substantial portion of crosslinking or setting and usually a complete setting prior to the forming and printing of the image.
  • thermosetting protective overcoating when the el ctrostatic printing is done in the manner described above, a thermosetting protective overcoating must be applied or else the printed matter lacks abrasion resistance, being easily removed or marred by handling.
  • thermosetting overcoating We have now discovered a novel method of electrostatic printing on metal substrates which eliminates the need for the thermosetting overcoating.
  • Our method involves providing the metal substrate with a coating comprising a dispersion of photoconductive Zinc oxide in an electrically insulating solution in a volatile organic solvent of an electrically insulating thermosetting resin which does not cross-link on air-drying.
  • a coating comprising a dispersion of photoconductive Zinc oxide in an electrically insulating solution in a volatile organic solvent of an electrically insulating thermosetting resin which does not cross-link on air-drying.
  • air-drying is meant permitting the solvent to evap rate at the ambient temperature.
  • the resin must be one which requires heat in order to under.- go any degree of setting.
  • Such resins are well known to those skilled in the art. While air drying is the preferred method of eliminating the solvent, the elimination of solvent may also be carried out at elevated temperatures if the temperature is sufliciently low enough to prevent any appreciable cross-linking of the resin.
  • the applied coating is air-dried to a tack-free, uncrosslinked film.
  • the coated plate is then charged and eX- posed to the image in the conventional manner.
  • the developer is applied conventionally. After the application of the developer, the developed coating is heated for the temperature and time required to set the particular thermosetting resin binder.
  • the resulting coated panel has the printed or developed matter firmly fixed. The rub resistance is excellent. The panel may be bent and otherwise worked without affecting the printing.
  • the zinc oxide particles are conventional photoconductive zinc oxide particles of the type described in the aforementioned Greig patents.
  • the binder resins must be thermosetting and electrically insulating. That is they must have high dielectric strengths of the same order as those of the thermoplastic resins described in said Greig patents.
  • the thermosetting resin must be one which while air-drying to a tack-free film does not undergo any cross-linking unless heat is applied.
  • Classes of this type of thermosetting resin are well known in the art. They include ureaformaldehyde resins, triazine-formaldehyde resins, phenolic resins, epoxy resins, methylolated acrylamide resins, styrenated alkyds and m'ethacrylated alkyds.
  • the coated panels are often piled in stacks prior to printing. Accordingly, it is preferable that the coatings have good block resistance.
  • Block resistance is determined by placing the coated surfaces of two panels face to face and applying a given pressure per unit area at a given temperature. If the surfaces do not stick together, then the coating is said to have a block resistance greater than the appled pressure at the temperature. When the panels are to be stacked during the printing process, it is preferable that the coatings have a block resistance greater than 1.5 lbs./ sq. in. at 25 C.
  • the developers used in this invention are preferably liquid developers.
  • Conventional liquid developers e.g., the
  • liquid developers of Patent No. 2,907,674 which are' charged particles dispersed in an insulating liquid of high volume resistivity e.g., toluene, cyclohexane, n-pentane and carbon tetrachloride may be used.
  • insulating liquid of high volume resistivity e.g., toluene, cyclohexane, n-pentane and carbon tetrachloride
  • Other suitable liquid developers are those described in Patent No. 3,078,231.
  • a dispersion of 1 g. of peacock blue pigment in 9 g. of mineral oil is in turn dispersed in 10,000 ml.
  • the developed image appears as blue printing on the white background.
  • the panel is then baked at 350 F. for /2 hour to cure the thermosetting coating and to fuse the deposited developer to the coating.
  • the coating is hard, tough and well cured, and the developer which is incorporated into the cured coating displays excellent ad hesion and rub-resistance.
  • Methylon 75108 Phenolic resin consisting of a mixture of the alkyl ethers of mono-, diand trimethylol phenol, the tri-component predominating, prepared in accordance with US. Patent No. 2,579,330, par- A 1:1 mixture of toluene and ethyl acetate in an amount sufficient to reduce the viscosity of the composition to 25 seconds on a Ford No. 4 Cup.
  • Epon 1007 epoxy resin, formed by the reaction of epichlorohydrin and Bisphenol A, having an average molecular weight of 2625, an epoxide equivalent weight of l5502200, a hydroxyl equivalent weight of 200 and 1.3 to 1.7 epoxides per molecule
  • Epon 1007 epoxy resin, formed by the reaction of epichlorohydrin and Bisphenol A, having an average molecular weight of 2625, an epoxide equivalent weight of l5502200, a hydroxyl equivalent weight of 200 and 1.3 to 1.7 epoxides per molecule
  • Zinc oxide (photoconductive) 50 0.12% solution in methanol of methylene blue dye 2.0
  • Styrenated 60% oil length phthalic alkyd resin having a 1:1, styrenezmodified alkyd content, the oil modifying the alkyd being a 1:1, soya-dehydrated castor oil blend Zinc oxide (photoconductive) 50 0.12% solution in methanol of methylene blue dye 2.0 and, xylene, in an amount sufficient to reduce the viscosity of the composition to 25 seconds on a Ford No. 4 Cup.
  • the process of this invention may be used on a wide variety of metal substrates such as aluminum, copper, brass and steel plates.
  • a process for forming a visible image on metal substrates consisting of the steps of (A) coating a surface of the metal substrate with a composition comprising a dispersion of photo-conductive zinc oxide in an electrically insulating filmforming thermosetting resin, selected from the group consisting of urea-formaldehyde resins, triazineformaldehyde resins, phenolic resins, epoxy resins, methylolated acrylamide resins, styrenated alkyds and methacrylated alkyds, which does not cross-link on air-drying in a volatile organic solvent,
  • thermosetting resinous film then simultaneously fixing the deposited developer and setting said thermosetting resinous film by heating at 350 F. for 30 minutes.
  • thermosetting resin is one which gives uncross-linked films upon airdrying having a block resistance greater than 1.5 1bs./sq. in. at 25 C.
  • the resin is a copolymer comprising the polymerization product of 75% styrene, 15% acrylamide, 7% ethyl acrylate and 3% methacrylic acid.

Description

United States Patent 3,401,037 ELECTROSTATIC PRINTING 0N METAL SUBSTRATES Jerome Roteman, Freehold, N.J., and Sebastian T. Brancato, Queens Village, N.Y., assignors to Interchemical Corporation, New York, N.Y., a corporation of Ohio No Drawing. Filed Nov. 25, 1964, Ser. No. 414,024 5 Claims. (Cl. 96-1) ABSTRACT OF THE DISCLOSURE An electrostatic printing process for developing a visible image on a metal substrate carrying a coating comprising a dispersion of photoconductive zinc oxide in a vehicle of an electrically insulated, air-dried, tack free, uncross-linked film of a thermosetting resin in a volatile organic solvent. The coated film is charged and the image formed in the conventional manner. The image is developed and the film simultaneously cured by exposure to heat.
This invention relates to electrostatic printing and particularly to electrostatic printing on metal substrates.
An electrostatic printing process is a process for producing a visibile image or copy by converting a light image or signal into an electrostatic charge pattern on an electrically insulating base. The charge pattern is then converted or developed into a visible image by the application thereto of electrically-attractable particles. A typical electrostatic printing process utilizing a photoconducting insulating stratum includes first producing a blanket electrostatic charge on the surface of the photoconducting stratum. The electrostatic charge may be stored on th surface for a time in the dark. Within the period in which a substantial charge remains, a light image is focused on the charged surface, discharging the portions of the surface irradiated with light, leaving the remainder of the surface in a charged condition, and thereby forming an electrostatic image thereon. The electrostatic image is rendered visible by applying to the electrostatic image a developer substance, such as a pigmented thermoplastic resin powder, which is held electrostatically to the charged areas of the surface. The visible image thus formed may be fixed directly to the surface, for example, by fusing the image thereto.
A process of electrostatic printing in which the thermoplastic resin powder is fused directly to the surface of the stratum is described in US. Patents 3,052,539 and 3,052,540, both to H. G. Greig.
Attempts have been made to utilize recording elements of the type described in the Greig patents in printing on tinplate and other metal substrates with less than fully desirable results. In such methods, photoconductive zinc oxide particles are usually dispersed in an electrically insulating thermoplastic binder and coated on the metal substrate. The electrostatic image is then formed and developed or printed, after which a clear thermosetting protective overcoating is applied. There have been some instances where thermosetting binders have been considered in place of the thermoplastic binders. However, these thermosetting binders have always been heated to effect'at leasta substantial portion of crosslinking or setting and usually a complete setting prior to the forming and printing of the image.
Irrespective of whether the binder is thermoplastic or thermosetting, we have found that when the el ctrostatic printing is done in the manner described above, a thermosetting protective overcoating must be applied or else the printed matter lacks abrasion resistance, being easily removed or marred by handling.
We have now discovered a novel method of electrostatic printing on metal substrates which eliminates the need for the thermosetting overcoating.
Our method involves providing the metal substrate with a coating comprising a dispersion of photoconductive Zinc oxide in an electrically insulating solution in a volatile organic solvent of an electrically insulating thermosetting resin which does not cross-link on air-drying. (By air-drying, is meant permitting the solvent to evap rate at the ambient temperature.) In other words, the resin must be one which requires heat in order to under.- go any degree of setting. Such resins are well known to those skilled in the art. While air drying is the preferred method of eliminating the solvent, the elimination of solvent may also be carried out at elevated temperatures if the temperature is sufliciently low enough to prevent any appreciable cross-linking of the resin.
The applied coating is air-dried to a tack-free, uncrosslinked film. The coated plate is then charged and eX- posed to the image in the conventional manner. The developer is applied conventionally. After the application of the developer, the developed coating is heated for the temperature and time required to set the particular thermosetting resin binder. The resulting coated panel has the printed or developed matter firmly fixed. The rub resistance is excellent. The panel may be bent and otherwise worked without affecting the printing.
The zinc oxide particles are conventional photoconductive zinc oxide particles of the type described in the aforementioned Greig patents.
The binder resins must be thermosetting and electrically insulating. That is they must have high dielectric strengths of the same order as those of the thermoplastic resins described in said Greig patents. In addition, the thermosetting resin must be one which while air-drying to a tack-free film does not undergo any cross-linking unless heat is applied. Classes of this type of thermosetting resin are well known in the art. They include ureaformaldehyde resins, triazine-formaldehyde resins, phenolic resins, epoxy resins, methylolated acrylamide resins, styrenated alkyds and m'ethacrylated alkyds.
During the printing of metals which are to be used in cans and containers, the coated panels are often piled in stacks prior to printing. Accordingly, it is preferable that the coatings have good block resistance.
Block resistance is determined by placing the coated surfaces of two panels face to face and applying a given pressure per unit area at a given temperature. If the surfaces do not stick together, then the coating is said to have a block resistance greater than the appled pressure at the temperature. When the panels are to be stacked during the printing process, it is preferable that the coatings have a block resistance greater than 1.5 lbs./ sq. in. at 25 C.
The developers used in this invention are preferably liquid developers. Conventional liquid developers e.g., the
liquid developers of Patent No. 2,907,674 which are' charged particles dispersed in an insulating liquid of high volume resistivity e.g., toluene, cyclohexane, n-pentane and carbon tetrachloride may be used. Other suitable liquid developers are those described in Patent No. 3,078,231.
While the preferred embodiments of this invention have been described in terms of liquid developers, it should be clear that the conventional powder developers may be used in place of the liquid developers. When powders are used the exposure and printing procedures of US. Patent No. 3,052,539 as well as the powder developers described in said patent may be used.
The following examples will further illustrate the practice of this invention. Unless otherwise set forth, all proportions in this specification and claims are by weight.
3 EXAMPLE 1- The following mixtureis ball milled to a smooth consistency:
Parts by weight A 48% solution in 1:1 xylene: butanol solvent of butoxy-methylolated acrylamide copolymer consisting of the reaction product of a 30% solution of formaldehyde in butanol with a copolymer of 75% styrene, acrylamide, 7% ethyl acrylate and 3% methacrylic acid; the formaldehyde solution: copolymer ratio is 1:3 Zinc oxide (photoconductive) A 0.12% solution in methanol of methylene blue dye 2.0
Then, sulficient xylene is added to reduce the viscosity of the mixture to 25 sec. on a Ford No. 4 Cup. The mixture is then sprayed by conventional apparatus on to tinplate panel and permitted to air-dry at the ambient temperature for about 2 to 3 hours. The resulting white coating is tack-free and has block resistance of about two pounds per square inch at room temperature. In order to print on the panel electrostatically, the coating on the panel is charged negatively in accordance with the procedure of US. Patent No. 2,907,674 and exposed to a positive transparency of the image to be printed. Then, following the procedure of said patent, a liquid developer of the following composition is applied to the plate:
A dispersion of 1 g. of peacock blue pigment in 9 g. of mineral oil is in turn dispersed in 10,000 ml. Isopar G solvent containing 7 g. of manganese naphthenate (aliphatic hydrocarbon solvent having a boiling range of 315-350 F. and a K. B. Value of 27.4.)
The developed image appears as blue printing on the white background. The panel is then baked at 350 F. for /2 hour to cure the thermosetting coating and to fuse the deposited developer to the coating. The coating is hard, tough and well cured, and the developer which is incorporated into the cured coating displays excellent ad hesion and rub-resistance.
EXAMPLE 2 Example 1 is repeated using the same procedure conditions, ingredients and proportions except that in the coating, the following formulation is used:
Parts by weight Methylon 75108 (Phenolic resin consisting of a mixture of the alkyl ethers of mono-, diand trimethylol phenol, the tri-component predominating, prepared in accordance with US. Patent No. 2,579,330, par- A 1:1 mixture of toluene and ethyl acetate in an amount sufficient to reduce the viscosity of the composition to 25 seconds on a Ford No. 4 Cup.
The results are substantially the same as in Example 1.
EXAMPLE 3 Example 1 is repeated using the same procedure, conditions, ingredients and proportions except that in the coating, the following formulation is used:
Parts by weight Epon 1007 (Epoxy resin, formed by the reaction of epichlorohydrin and Bisphenol A, having an average molecular weight of 2625, an epoxide equivalent weight of l5502200, a hydroxyl equivalent weight of 200 and 1.3 to 1.7 epoxides per molecule Urea-formaldehyde 30 Zinc oxide (photoconductive) 50 0.12% solution in methanol of methylene blue dye 2.0
and, A 1:1 mixture of xylene and methyl isobutyl ketone in an amount sufiicient to reduce the viscosity of the composition to 25 seconds on a Ford No. 4 Cup.
The results are substantially the same as in Example 1.
EXAMPLE 4 Example 1 is repeated using the same procedure, conditions, ingredients and proportions except that in the coating, the following formulation is used:
Parts by weight Styrenated 60% oil length phthalic alkyd resin having a 1:1, styrenezmodified alkyd content, the oil modifying the alkyd being a 1:1, soya-dehydrated castor oil blend Zinc oxide (photoconductive) 50 0.12% solution in methanol of methylene blue dye 2.0 and, xylene, in an amount sufficient to reduce the viscosity of the composition to 25 seconds on a Ford No. 4 Cup.
The results are substantially the same as in Example 1.
EXAMPLE 5 Example 1 is repeated using the same procedure, conditions, ingredients and proportions, except that in the coating, the following formulation is used:
Parts by weight A methacrylated 30% oil length alkyd resin, the methyl methacrylate content of which is 35% and the modifying oil of which is dehydrated castor oil 100 Zinc oxide (photoconductive) 50 0.12% solution in methanol of Methylene Blue dye 2.0 and, Xylene in an amount sufficient to reduce the viscosity of the composition to 25 seconds on a Ford No. 4 Cup.
The results are substantially the same as in Example 1.
In addition to tin-plate as described in the examples, the process of this invention may be used on a wide variety of metal substrates such as aluminum, copper, brass and steel plates.
While there have been described what is at present considered to be the preferred embodiments of this invention, it will be obvious to those skilled in the art that various changes and modifications may be made therein without departing from the invention, and it is, therefore, aimed to cover all such changes and modifications as fall within the true spirit and scope of the invention.
We claim:
1. A process for forming a visible image on metal substrates consisting of the steps of (A) coating a surface of the metal substrate with a composition comprising a dispersion of photo-conductive zinc oxide in an electrically insulating filmforming thermosetting resin, selected from the group consisting of urea-formaldehyde resins, triazineformaldehyde resins, phenolic resins, epoxy resins, methylolated acrylamide resins, styrenated alkyds and methacrylated alkyds, which does not cross-link on air-drying in a volatile organic solvent,
(B) air-drying the applied coating to a tack-free uncross-linked film,
(C) forming a pattern of electrostatic charges corresponding to said image on the surface of said coating,
(D) developing said pattern by depositing a finelydivided developer substance on the surface bearing said pattern in a configuration conforming with said pattern, and
5 (E) then simultaneously fixing the deposited developer and setting said thermosetting resinous film by heating at 350 F. for 30 minutes.
2. The process of claim 1, wherein the developer is a dispersion of finely-divided charged pigment particles in an electrically insulating liquid.
3. The process of claim 1, wherein the thermosetting resin is one which gives uncross-linked films upon airdrying having a block resistance greater than 1.5 1bs./sq. in. at 25 C.
4. The process of claim '1, wherein the resin is a copolymer comprising the polymerization product of 75% styrene, 15% acrylamide, 7% ethyl acrylate and 3% methacrylic acid.
plate.
6 References Cited UNITED STATES PATENTS Van Dorn et al 961.8 Kucera 961.8 Semegen 117-76 Middleton et al 96-15 Metcalfe et a1 961 Wolff u 96-l.8 Sciambi 961.5 Gray 961.5 Fox 96--1.5
NORMAN G. TORCHIN, Primary Examiner. 5. The proces of claim 1, wherein said metal is tin- 15 C. E, VAN HORN, Assistant Examiner.
US414024A 1964-11-25 1964-11-25 Electrostatic printing on metal substrates Expired - Lifetime US3401037A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US414024A US3401037A (en) 1964-11-25 1964-11-25 Electrostatic printing on metal substrates

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US414024A US3401037A (en) 1964-11-25 1964-11-25 Electrostatic printing on metal substrates

Publications (1)

Publication Number Publication Date
US3401037A true US3401037A (en) 1968-09-10

Family

ID=23639649

Family Applications (1)

Application Number Title Priority Date Filing Date
US414024A Expired - Lifetime US3401037A (en) 1964-11-25 1964-11-25 Electrostatic printing on metal substrates

Country Status (1)

Country Link
US (1) US3401037A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3519421A (en) * 1967-09-26 1970-07-07 Gaf Corp Electrophotographic recording material
US3620729A (en) * 1969-08-28 1971-11-16 Nat Starch Chem Corp Electrophotographic coating compositions employing styrene terpolymers as binders
US3671646A (en) * 1968-07-27 1972-06-20 Mitsubishi Paper Mills Ltd Liquid developers for electrostatic photography
US4105448A (en) * 1974-08-23 1978-08-08 Fuji Photo Film Co., Ltd. Electrophotographic photosensitive layer and marking method
US4748099A (en) * 1978-02-07 1988-05-31 Konishiroku Photo Industry Co., Ltd. Process for forming printing plate using an electrophotographic material for obtaining toner image
US20130017405A1 (en) * 2010-05-28 2013-01-17 The Johns Hopkins University Self-Healing Coatings

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2937944A (en) * 1957-11-20 1960-05-24 Haloid Xerox Inc Xerographic light-sensitive member and process therefor
US2959481A (en) * 1958-12-18 1960-11-08 Bruning Charles Co Inc Electrophotographic recording member and process of producing same
US2973284A (en) * 1957-04-30 1961-02-28 Goodrich Co B F Leather-like material
US3121006A (en) * 1957-06-26 1964-02-11 Xerox Corp Photo-active member for xerography
US3174855A (en) * 1961-02-23 1965-03-23 Xerox Corp Method for a production of a xerographic plate
US3197043A (en) * 1962-03-15 1965-07-27 Brewster Machine Co Bale buncher attachment for hay balers
US3226227A (en) * 1960-09-02 1965-12-28 Rca Corp Method of producing a solvent-resistant pattern using developed electrostatic image formation techniques
US3231374A (en) * 1960-09-02 1966-01-25 Rca Corp Methods for preparing etch resists using an electrostatic image developer composition
US3240597A (en) * 1961-08-21 1966-03-15 Eastman Kodak Co Photoconducting polymers for preparing electrophotographic materials

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2973284A (en) * 1957-04-30 1961-02-28 Goodrich Co B F Leather-like material
US3121006A (en) * 1957-06-26 1964-02-11 Xerox Corp Photo-active member for xerography
US2937944A (en) * 1957-11-20 1960-05-24 Haloid Xerox Inc Xerographic light-sensitive member and process therefor
US2959481A (en) * 1958-12-18 1960-11-08 Bruning Charles Co Inc Electrophotographic recording member and process of producing same
US3226227A (en) * 1960-09-02 1965-12-28 Rca Corp Method of producing a solvent-resistant pattern using developed electrostatic image formation techniques
US3231374A (en) * 1960-09-02 1966-01-25 Rca Corp Methods for preparing etch resists using an electrostatic image developer composition
US3174855A (en) * 1961-02-23 1965-03-23 Xerox Corp Method for a production of a xerographic plate
US3240597A (en) * 1961-08-21 1966-03-15 Eastman Kodak Co Photoconducting polymers for preparing electrophotographic materials
US3197043A (en) * 1962-03-15 1965-07-27 Brewster Machine Co Bale buncher attachment for hay balers

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3519421A (en) * 1967-09-26 1970-07-07 Gaf Corp Electrophotographic recording material
US3671646A (en) * 1968-07-27 1972-06-20 Mitsubishi Paper Mills Ltd Liquid developers for electrostatic photography
US3620729A (en) * 1969-08-28 1971-11-16 Nat Starch Chem Corp Electrophotographic coating compositions employing styrene terpolymers as binders
US4105448A (en) * 1974-08-23 1978-08-08 Fuji Photo Film Co., Ltd. Electrophotographic photosensitive layer and marking method
US4748099A (en) * 1978-02-07 1988-05-31 Konishiroku Photo Industry Co., Ltd. Process for forming printing plate using an electrophotographic material for obtaining toner image
US20130017405A1 (en) * 2010-05-28 2013-01-17 The Johns Hopkins University Self-Healing Coatings

Similar Documents

Publication Publication Date Title
US4314013A (en) Particle formation by double encapsulation
US3411936A (en) Developing electrostatic images with a liquid developer containing tetraphenyl tin or zirconyl 2-ethylhexoate
US2946682A (en) Electrostatic printing
EP0289348B1 (en) Photoresponsive imaging members with high molecular weight polysilylene hole transporting compositions
US2993787A (en) Electrostatic printing
US4105448A (en) Electrophotographic photosensitive layer and marking method
JPS6172256A (en) Manufacture of overcoated xerographic image forming member
US3207601A (en) Methods of preparing etch resists using an electrostatic image developer composition including a resin hardener
US3401037A (en) Electrostatic printing on metal substrates
US3215527A (en) Method for preparing cured polymeric etch resists using a xerographic developer containing a curable polymer
US3226227A (en) Method of producing a solvent-resistant pattern using developed electrostatic image formation techniques
US3926629A (en) Electrophotographic method and plate employing a phthaldcyanine polymer
US4062681A (en) Electrophotographic element having a hydrophobic, cured, highly cross-linked polymeric overcoat layer
US3373140A (en) Thermoplastic epoxy resin photoconductors
US5264312A (en) Charge transporting layers formed from curable compositions
US3617265A (en) Method for preparing a resin overcoated electrophotographic plate
US3152895A (en) Coating composition for the production of electrophotographic recording members
US3447957A (en) Method of making a smooth surfaced adhesive binder xerographic plate
JPH11271991A (en) Electrophotographic photoreceptor having charge generating layer by blending polymer
US3368893A (en) Electrophotographic method of preparing etchable printing plates
US3928655A (en) Electrostatic powder coating method
US3511648A (en) Electrophotographic coatings
US3041168A (en) Electrostatic printing
US3682631A (en) Method of forming an electrophotographic layer containing a benzoguanamine resin binder
US3192043A (en) Method for developing and fixing electrostatic images in initially partially cured base elements