US3260612A - Thermographic recording process and heat-sensitive elements therefor - Google Patents

Thermographic recording process and heat-sensitive elements therefor Download PDF

Info

Publication number
US3260612A
US3260612A US211927A US21192762A US3260612A US 3260612 A US3260612 A US 3260612A US 211927 A US211927 A US 211927A US 21192762 A US21192762 A US 21192762A US 3260612 A US3260612 A US 3260612A
Authority
US
United States
Prior art keywords
heat
sensitive
temperature
original
tackifying
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
US211927A
Other languages
English (en)
Inventor
William J Dulmage
Sterling S Sweet
William A Light
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.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
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
Priority to NL294592D priority Critical patent/NL294592A/xx
Priority to FRJ8061696*8A priority patent/FR95952E/fr
Priority to NL294591D priority patent/NL294591A/xx
Priority to DE19621421406 priority patent/DE1421406A1/de
Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co
Priority to US211927A priority patent/US3260612A/en
Priority to FR903911A priority patent/FR1472015A/fr
Priority to GB27283/62A priority patent/GB1015925A/en
Priority to GB23939/65A priority patent/GB1015926A/en
Priority to DK283963A priority patent/DK107814C/da
Priority to DK283863AA priority patent/DK115123B/da
Priority to AT485563A priority patent/AT264552B/de
Priority to AT662267A priority patent/AT290295B/de
Priority to AT789265A priority patent/AT265019B/de
Priority to DE19631471664 priority patent/DE1471664A1/de
Priority to ES289370A priority patent/ES289370A1/es
Priority to CH367666A priority patent/CH449065A/fr
Priority to CH793763A priority patent/CH428804A/fr
Priority to BE645645A priority patent/BE645645A/xx
Priority to CH1022364A priority patent/CH458412A/fr
Priority to US46335465 priority patent/US3342623A/en
Application granted granted Critical
Publication of US3260612A publication Critical patent/US3260612A/en
Priority to MY1966135A priority patent/MY6600135A/xx
Priority to US614571A priority patent/US3387974A/en
Priority to MY1969127A priority patent/MY6900127A/xx
Priority to MY257/74A priority patent/MY7400257A/xx
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/398—Processes based on the production of stickiness patterns using powders
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C1/00—Forme preparation
    • B41C1/10—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/025—Duplicating or marking methods; Sheet materials for use therein by transferring ink from the master sheet
    • B41M5/04—Duplicating or marking methods; Sheet materials for use therein by transferring ink from the master sheet using solvent-soluble dyestuffs on the master sheets, e.g. alcohol-soluble
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
    • G03C8/42—Structural details
    • G03C8/52—Bases or auxiliary layers; Substances therefor
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F10/00—Thin magnetic films, e.g. of one-domain structure
    • H01F10/08—Thin magnetic films, e.g. of one-domain structure characterised by magnetic layers
    • H01F10/10—Thin magnetic films, e.g. of one-domain structure characterised by magnetic layers characterised by the composition
    • H01F10/12—Thin magnetic films, e.g. of one-domain structure characterised by magnetic layers characterised by the composition being metals or alloys
    • H01F10/16—Thin magnetic films, e.g. of one-domain structure characterised by magnetic layers characterised by the composition being metals or alloys containing cobalt
    • 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
    • Y10S101/00—Printing
    • Y10S101/37—Printing employing electrostatic force

Definitions

  • thermographic materials and processes relate to improved thermographic materials and processes. More particularly, the invention relates to thermographic methods and materials in which a latent image can be produced on a heat-sensitive layer, and after activation can be either transferred or developed in situ at a temperature lower than the activating temperature.
  • thermogr-aphic processes there have been two rather widely used general types of thermogr-aphic processes.
  • the first of these comprises direct copying processes in which a visible image is produced directly on a heat-sensitive element which then becomes a final copy.
  • This has the disadvantage that the final copy remains heat-sensitive in the unactivated background area and is subject to subsequent activation.
  • the copy obtained is on a thin, coated heat-sensitive sheet that does not stand up well under ordinary use.
  • a second type of process now in general use comprises preferentially heating only the image areas of a heatsensitive layer of a waxy material to melting temperature, and while the image areas are preferentially heated, transferring melted Wax from the image areas to a receiving sheet. Wax in the lower temperature background areas is not melted, and so does not transfer.
  • a 3-ply combination comprising an original document, a receiving sheet, and a heat-sensitive matrix, is exposed to infrared radiation which heats the printed areas in the document. This then melts the material in corresponding image areas of the matrix.
  • the receiving sheet During exposure, the receiving sheet must be in contact with the heat-sensitive material in order to effect a transfer of material from the matrix while its image areas are preferentially heated above the melting point of the heat-sensitive material. To obtain a right-reading copy in processes of this type, the receiving sheet is usually placed between the original and the heat-sensitive layer. Because the receiving sheet must be between the document in which heat is generated, and the heat-sensitive material to which the heat must be conducted, there is some thermal diffusion through the receiving sheet, and this causes considerable detriment to image definition. Because the transfer material may harden before the receiving sheet and the matrix can be separated, the receiving sheet often has to be broken away or fractured from the residual resin or wax layer of the heat-sensitive element. This breaking away results in uneven density and poor definition in the final copy due to irregular breakage characteristics.
  • An object of the present invention is to provide novel thermographic materials and methods which overcome many of the disadvantages of prior-art methods and offer advantages not heretofore available in thermographic processes and materials.
  • Another object of the invention is to provide thermographic materials and processes employing a heat-sensitive layer in which image areas can be activated at a temperature well above room temperature .and after such activation can subsequently be either deice veloped in the image areas of the heat-sensitive layer or transferred to a receiving surface from image areas of the heat-sensitive layer, while the entire heat-sensitive element is at a uniform temperature substantially below the original activation temperature.
  • Certain embodiments of the invention provide a dry process for reproduction of multiple copies from a single activated heat-sensitive element. The copies can be on regular white stationery or the like.
  • the invention provides means by which a heatsensitive transfer matrix can be activated with its heatsensitive layer in direct face-to-face contact with the document being copied, thus avoiding thermal diffusion and obtaining a well resolved latent image in the layer. Copies can be made from a thermographic element after activation without the need for preferential heating of the image areas during the development or transfer step of the process.
  • the present invention enables preparation of multiple copies from a single thermographic heat-sensitive element. It enables production of prints of excellent quality and good stability, and at materially reduced costs per copy.
  • FIG. 1 is a schematic elevational view showing a method of producing an image directly on a heat-sensitive element of the present invention
  • FIG. 2 is a schematic elevational view of a method of exposing a heat-sensitive element of the present invention
  • FIG. 2A illustrates a method of transfer of material from the image areas of the exposed heat-sensitive element of FIG. 2 to a receiving copy sheet
  • FIG. 3 is a schematic elevational view showing a tandem arrangement for exposure of a heat-sensitive element with subsequent transfer of the image areas thereof to a receiving copy sheet.
  • FIG. 4 is a schematic cutaway view of a heat-sensitive element embodying certain preferred embodiments of the invention.
  • the novel heat-sensitive element according to the invention comprises a support, usually a flexible backing such as paper, on which is coated a layer of thermoplastic material in a state of partial or complete crystallization.
  • the thermoplastic material is substantially non-tacky, non-viscous, and dry at ambient temperatures.
  • the material in this layer undergoes transition to an amorphous state and thereafter, for a substantial period, has a tackifying temperature substantially below the original tackifying temperature.
  • the tackified image area can be developed directly on the heat-sensitive element by adhering powders having optical density to the tackified areas; or the tackified material can be transferred from the image areas to a receiving surface, and then developed on the receiving surface, and then developed on the receiving surface while still tacky; or, if the tacky material in the activated areas of the heatsensitive layer has optical density, it can be transferred from the image areas to a receiving surface to produce a printed image on the receiving surface.
  • the development or transfer step can be done after the activation step without the need for any preferential heating of the image areas during the development or transfer step.
  • Thermoplastic compositions useful in the heat-sensitive elements of the present invention have the characteristic property of remaining in a state having a reduced tackifying temperature for a substantial time after once being heated to the original tackifying temperature.
  • the thermoplastic materials most preferred for making the heat-sensitive thermoplastic layer are polymer-containing materials having this property.
  • thermoplastic material of the heat-sensitive layer A great variety of polymers are available for making the thermoplastic material of the heat-sensitive layer.
  • the polymer-containing thermoplastic materials useful in the invention can be divided into two general types: (a) those in which the polymer component itself is partially or completely crystallized (of course, a partially crystallized mixture of amorphous and crystalline polymers can be used) and (b) those in which the polymer component is substantially amorphous but non-tacky up to activation temperature, and non-polymeric crystalloid is the crystallized component. This crystalloid melts at the activating temperature and blends with the amorphous polymer to make a mixture having a lower tackifying temperature.
  • the heat-sensitive layer of the heat-sensitive element comprises a coating of one of these thermoplastic materials developed to a non-tacky state of complete, or at least partial crystallization. In this state of complete or partial crystallization, the material has a tackifying temperature substantially higher than the tackifying temperature of the same material in completely amorphous state.
  • these activated areas can usually be retackified at a temperature substantially below the original tackifying temperature.
  • a heat-sensitive layer having an original tackifying temperature of 120 C. might be activated in the image areas, and after some time material in these areas might partially recrystallize to a non-tacky state at room temperature.
  • these activated areas could be retackified at temperatures well below 120 C., say at 70 or 80 C, This could be done, for example, by calendering the heat-sensitive element through rolls heated to the lower tackifying temperature, or by any other means for uniformly heating the element to the lower tackifying temperature.
  • the background areas in the heat-sensitive layer remain unactivated at such lower temperatures.
  • the original tackifying temperature of some partially crystallized heat-sensitive layers can be increased by annealing.
  • annealing we refer to the process of relieving intercrystalline stresses and the ripening and perfection of the crystalline phase of the orystallizable polymers.
  • Such treatment can cause a substantial increase in the melting point of polymers.
  • Crystallization may be promoted in many ways such as heating or stretching so as to orient, or cooling to an efficient nuclea-ting temperature by passing through cold calender rolls followed by heating, etc. or by treating with solvent or solvent v-ap-or. Any of these treatments Will affect the tackifying point.
  • the annealing may be done with partially crystalline polymeric films like the heat sensitive coatings of our invention, by heat-ing the coated element above the glass transition temperature of the thermoplastic composition.
  • the annealing is started at a temperature below the initial tackifying temperature and the heat treatment temperature may be raised fairly rapidly since the annealing process immediately begins to raise the melting point. Consequently the highest temperature during annealing may be well above the initial tackifying point but at least a few degrees below the ultimate or highest melting point characteristic of the crystalline polymers.
  • the total annealing, or at least that much required to give the matrix the desired tackifying temperature, may be completed in less than a minute in some cases or it may require several hours in others.
  • a crystalline polymer-containing heat-sensitive layer during manufacture to a crystalline state having an original tackifying temperature higher than the tackifying temperature of the highest state of crystallization that the polymer will attain at temperatures below 50 C. upon recrystallization after being once activated by transition to the amorphous state.
  • a matrix with such an annealed layer can be re-activated, even after material in the activated image areas has recrystallized at room temperatures, simply by uniformly heating the matrix to a temperature below the original tackifying temperature of the heat-sensitive layer, but above the tackifying temperature of the recrystallized material in the image areas.
  • the annealing process can be used to reclaim used, that is, exposed matrices from which the number of prior transfers made has been sufficiently small not to have re-- moved all of the heat-sensitive coating in the image areas.
  • reclaim used that is, exposed matrices from which the number of prior transfers made has been sufficiently small not to have re-- moved all of the heat-sensitive coating in the image areas.
  • a heat-sensitive layer In order to prevent unintentional activation of the heatsensitive layer by extremely high climatic temperatures, we prefer to use a heat-sensitive layer with an original tackifying temperature above 50 C.
  • a heat-sensitive layer For use in most of the thermographic process machines now in use, which are designed to produce activating temperatures in a range between about 50 C. and 200 C., a heat-sensitive layer would be chosen with an original tackifying temperature in that range.
  • a heat-sensitive material In some processes, it is convenient to develop or transfer the material of the activated image areas at usual room temperature and in such cases, a heat-sensitive material would be chosen having a tackifying temperature after activation at least as low as about 15 C.
  • thermoplastic mate-rial in the heat-sensitive layer must, after activation, be tackifiable at a temperature substantially below the original tackifying temperature, that the material of the heat-sensitive layer must have a glass transition temperature after activation that is substantially below the original tackifying temperature of the heat-sensitive layer.
  • tackifying temperature is meant the lowest temperature (or temperature range) at which the material in the state being described .will become tacky.
  • the tackifying temperature is the first-order transition temper-ature, and for a completely amorphous thermoplastic polymer composition, it is the second-order transition temperature, sometimes called glass transition temperature.
  • the tackifying temperature will be a pseudo- :first-order transition temperature, more or less below the real first-order transition temperature depending upon the degree of crystallization.
  • tackifying temperature When a non-polymer crystalloid melts and blends with an amorphous polymer the glass transition temperature is lowered, as is the tackifying temperature. Because the same term is used herein with reference to thermoplastic compositions in all three states, amorphous, crystallized, and partly crystallized including partly crystallized compositions containing amorphous polymers and non-polymeric crystalloids, the general term tackifying temperature is most appropriate.
  • the thin, crystalline, heat-sensitive, polymeric films on which the utility of our heat-sensitive elements depends can be prepared using either crystalline or amorphous polymers chosen from a wide variety of linear, film-forming polymers and copolymers, such as polyvinyl derivatives, polyacrylic derivatives, polyesters, polyamides, polye-ster-amides, polycarbonates, polyethers (e.g., polyglycols), polyurethanes, polyureas, and the like.
  • amorphous polymers which can be used in admixture with nonpolymeric crystalloids to prepare the heat-sensitive layers of the present invention:
  • Atactic polystyrene (2) Poly(vinyl acetate), medium-viscosity grade. (3) Butadiene, styrene copolymer of 45:55 ratio, (Goodyear Tire and Rubber Co.s Pliolite S-7.
  • Poly(alkyl methacrylates), lowand mediumviscosity grade such as polymethyl methacrylate, polyethyl methacrylate, polybutyl methacrylate, etc.
  • Vinyl chloride, vinyl acetate copolymer of about 87: 13 ratio (Union Carbides Vinylite VYLF).
  • Phenol-formaldehyde resins (noncrosslinked), softening point range 70110 C. Novolacs).
  • the heat-sensitive layers of our invention can be coated from crystalline polymeric compositions comprising a combination of an amorphous, linear, filmforming polymer, representing for example one of the -above classes and a nonpolymeric crystalloid to yield a crystalline composition having tackifying point, glass transition temperature, and melt viscosity within the ranges specified for our heat-sensitive compositions.
  • the useful nonpolymeric crystalloids are compounds which melt in the range of 50 to 200 C.
  • Suitable nonpolymeric crystalloids can be chosen from the following representative examples, the specific composition and the ratio of polymer to crystalloid depending on the properties of the polymer with which it will be admixed and the temperature range, the desired tackifying point, glass transition point, melt viscosity, rate of crystallization and the like: Pentaerythritol tetraisobutyrate; 2,6 ditert-buyl-4-methylphenol; eugenol benzoate; triphenyl orthoformate; benzoin acetate; N- pentyl-1,8-naphthalimide; bis(o-methoxyphenyl) carbonate; eugenol cinnamate; 2,5,5-triphenyl-1,3-dioxalan-4- (Union Carbides one; bis(benzyloxy) diphenylmethane; 4-cyclohexylphenyl benzoate; 4-biphenylyl benzoate; pentachlorophenyl
  • our heat-sensitive, crystalline, polymeric compositions can comprise crystalline polymers, chosen for example from one of the previously mentioned classes of linear, film-forming, polymers and copolymers.
  • crystalline polymeric materials useful in the present invention are given in Table I below along with the tackifying point, melt-viscosity at the tackifying point, and intrinsic viscosity for the polymers.
  • the tackifying point shown in Table I is approximately the first order transition temperature of the pure polymer. In the heat-sensitive layerthe tackifying temperature may be modified, as by developing only partial crystallization in the layer, for instance. Melt viscosities shown are at the tackifying temperatures shown.
  • the letter A indicates a melt-viscosity in the range from about 50 to about 500 poises
  • the letter B indicates a melt-viscosity in the range from about 500 to about 100,000 poises.
  • the intrinsic viscosity is given as a measure of the degree of polymerization of the polymer. Intrinsic viscosity, accordingly, also is a reflection of the molecular weight of the polymer; that is to say, as intrinsic viscosity goes up, the molecular weight of the polymer is also higher, and likewise, where the intrinsic viscosity goes down, the
  • Typical polymers representative of those suitably employed in the present invention include the following:
  • thermographic element comprises a heat-sensitive coatable composition containing a polymeric component coated on a suitable support in a well-known manner, such as extrusion, hopper coating, dip coating, doctorblade coating, etc.
  • Suitable supports include paper, e.g., grease-proof paper, such as Folio Transparent Copy Greaseproof Paper sold by the Rhinelander Paper Com- Oil Orange 2311, .Ultra Blue 9775 A, and A20 Oil Blue Black B.
  • film base e.g., cellulose acetate, cellulose acetate butyrate, cellulose acetate propionate, etc.
  • polyester film base e.g., polyethylene terephthalate; etc.
  • Solvents to which we refer can include a number of hydrocarbon solvents, for example, benzene, toluene, etc.; ketones, such as acetone, Z-butanone, 4-methyl-2-pentanone, etc.; chlorinated hydrocarbons, such as methylene chloride, ethylene chloride, carbontetrachloride, and the like.
  • addenda to accomplish a variety of purposes, such as agents to modify the flexibility of the layer, to modify the surface characteristics, to impart color to the layer, to modify the adhesivity of the heat-sensitive layer to its support, and solid particle extenders to decrease the amount of polymer required.
  • the above addenda may, without particularly affecting crystallization, have beneficial effects to both surfaces of the heat-sensitive layer, for example, increasing its adhesion to its support while on the exterior surface enabling intimate contact between it and the original document during exposure, while preventing optical contact.
  • added addenda examples include tricresyl phosphate, poly(alkyl acrylate), dibutyl fumarate, menthol, diethyl phthalate, eugenol, isoeugenol, dibutyl phthalate, eugenol methyl ether, isoeugenol methyl ether, clay, glass beads, ground quartz, crosslinked poly(methyl methacrylate) beads, tritanium dioxide, zinc oxide, and infrared transparent dyes.
  • Suitable coloring addenda of this latter type include the following materials available from the Allied Chemical and Dye Corporation, for example, Azo Oil Black, Oil Black BT, Alizarin Blue G.R.L. Base, Oil Scarlet 60, Oil Red GRO, Oil Red 0, Plasto Oil MGS, Isosol Black,
  • coloring addenda include Nile Blue Hydroxide, Methyl Red, Prussian Blue Pigment, Iron Oxide, etc.
  • a single coating of the polymer-containing composition is normally made onto the support at a thickness to give a predetermined thickness when dried.
  • the layer can be built up of two or more thin coats.
  • the dry thickness of the heat-sensitive layer can vary over a wide range.
  • a suitable coating thickness can be in the range from about 0.05 to about 2.0 mils.
  • a preferred coating thickness was found to be in the range from about 0.1 to about 1.0 mil.
  • An especially convienient method for preferentially heating image areas in the heat-sensitive element to activation temperature is to contact the heat-sensitive element with a document to be copied and, while the two are in contact, to expose the document to infrared radiation which generates heat in the printed areas of the document. This generated heat is then transmitted to the corresponding areas on the heat-sensitive element and raises the temperature of those areas to activation temperature.
  • a heat-sensitive element for use in infrared exposure processes must contain no infrared-absorbing materials, or at least no materials that would generate enough heat during the period of infrared radiation to raise the temperature of the background areas in the heat-sensitive layer to activation temperature. Such elements are defined herein by the term infraredtransparent.
  • the original document can be placed on the reverse side of the heat-sensitive element with graphic portions of the document in contact with the support side of the element.
  • radiation would be directed onto the side of the element having the heat-sensitive coating.
  • An exposure of this type is referred to as bi-reflex exposure.
  • reflex exposure comprises placing the graphic portions of the original in contact with the heat-sensitive surface of the element.
  • the infrared radiation is usually directed onto the support side of the heat-sensitive element.
  • a third method called direct exposure comprises placing the heat-sensitive layer in direct contact with the reverse side of the document.
  • thermographic exposure is then directed onto the graphic side of the original.
  • the support for the element be heat-insulated so that heat transmitted to the element from the image area of the document during exposure will not be dissipated through the support.
  • Heat-insulating supports are sometimes advantageous in direct exposure methods. Other heatinsulating means may be used if the support does not provide sufficient insulation.
  • Suitable radiant energy for exposing the heat-sensitive elements in methods of document reproduction according to the present invention can be obtained from a number of sources, for example, a carbon arc, tungsten filament lamp, overvoltaged standard infrared ray lamp, etc. Normally, it is advisable with most sources of infrared radiation to employ suitable reflectors, filters, etc., so that radiations of suitable wavelength and intensity are obtained in a manner to give sufficient radiation in an instantaneous manner.
  • a convenient source of infrared radiation comprises a standard 500-watt infrared bulb with internal reflector, operated under overload conditions of at least about 800-watt input, and at a distance of from about one-half to about three inches from the printed graphic original.
  • Other sources having a high output of radiant energy, particularly wavelengths of less than 25,000 A. and capable of uniformly irradiating larger areas can also be used.
  • FIG. 1 Illustration of the invention is given in FIG. 1 in which the graphic original 1 is placed in contact with the heatsensitive element 2 wherein the graphic portions of said original are in contact with the support of said element.
  • the 2-ply combination is passed behind the drag roll 3 and given a bi-reflex exposure from an infrared radiation source 4 while pressed against a hollow drum 5.
  • the hollow drum or main roller is usually rubber covered and provided with a clamp (C) for holding the heatsensitive element and graphic original.
  • the infrared exposure produces tackiness in the heat-sensitive layer in the areas corresponding to the image areas of the original.
  • the element is then developed by dusting with a developing powder 8 as carried out by developing roll 6 and feed roll 7. These rolls effectively brush the tackified image areas of the heat-sensitive element 2 with the developing powder.
  • the first clean-up brush 9 and the second clean-up brush 10 remove the powdered developer 8 from the nonimage areas of the heat-sensitive layer.
  • Suitable developer powders can include practically any pulverizable powder having optical density, for example, lycopodium powder, talcum powder, sulfur, carbon dust, aluminum bronze powder, etc.
  • Powdered dyes can also be used or a resin can be used which may be dyed any color desired. For example, Vinsol resin or gum copal may be melted with a small proportion of nigrosine dye,
  • dyes which can be used comprise such dyes as Rhodamine, Victoria Blue, Victoria Green, Crystal Violet, Nigrosine, Methyl Violet, etc.
  • thermographic process of the present type can be used in thermographic process of the present type to produce lithographic masters, hectographic masters, etc.
  • FIG. 2 a heat-sensitive element 2 is placed in contact with a graphic original 1 with the printed characters of the original in contact with the heat-sensitive surface of said element and passed into contiguous relationship with an infrared transparent carrier belt 3a with the copying element being on the exposure side of said original 1. Exposure is then given by an infrared radiation source 4 to produce tackified areas in the heatsensitive layer of element 2 corresponding to the image areas of the original 1. Rollers 5, 6, 7 and 8 afiord carrier means past the infrared radiation source 4.
  • FIG. 2 a heat-sensitive element 2 is placed in contact with a graphic original 1 with the printed characters of the original in contact with the heat-sensitive surface of said element and passed into contiguous relationship with an infrared transparent carrier belt 3a with the copying element being on the exposure side of said original 1. Exposure is then given by an infrared radiation source 4 to produce tackified areas in the heatsensitive layer of element 2 corresponding to the image areas of the original 1. Rollers 5, 6, 7 and 8 af
  • the exposed heat-sensitive element 2 is placed with the heat-sensitive layer in contact with a copying sheet 9 and passed between pressure rollers 10 and 11 past deflector means 12 to produce a right-reading copy of the graphic original 1 in the copying sheet 9.
  • the time elapsed, after exposure and before transfer as illustrated in FIG. 2a can vary widely, as pointed out previously, depending upon the compostion employed in the heat-sensitive layer of element 2. According to the invention, repeated transfers can be made from the exposed element 2 without requiring re-exposure. The number of copies to be obtained from a single exposure will depend largely upon composition of the heat-sensitive layer of element 2, the heat-sensitive polymer incorporated therein, total time involved in the transfer series, type of equipment used, etc.
  • the heat-sensitive element 2 is carried on a supply roll and passed in contact with a graphic original 1 wherein the heat-sensitive layer of said element is in contact with the graphic side of said original.
  • the 2-ply combination is then passed over roller 6 past an infrared radiation source 4 to produce a latent thermo graphic image in said heat-sensitive element 2.
  • the heat-sensitive element 2 after exposure is passed between pressure transferring rollers 7 and 8 in contact with a strip of copying paper 9.
  • Guide roller maintains continuation of movement to afford opportunities for the windup of the copying material.
  • An adequate supply of copy or receiving paper is supplied by supply roll 11.
  • Example 1 A heat-sensitive element of the present invention was prepared as follows for use in a directdevelopment process.
  • the solution was then doctor-blade coated at 2 mils thickness on a sheet of greaseproof paper (sold under the trade name Folio Transparent Copy Greaseproof Paper by the Rhinelander Paper Company). After coating, the element was then dried overnight at room temperature. After the solvent was removed from the coating by drying, the element was annealed for about 16 hours at 70 C.
  • an original document was placed on the reverse side of the heat-sensitive element with the printed characters of the original in contact with the support of said element.
  • the 2-ply assembly was then exposed by directing the infrared radiation onto the coated side of the element.
  • the exposure comprised intense infrared irradiation using a standard 1000-watt tubular General Electric infrared bulb with elliptical reflector, operated under overload conditions, for example, from about 800 to 1460 watts and at a distance of about /2 inch from the exposing surface.
  • the radiation was absorbed by the printed characters of the original and converted into heat.
  • the heat being generated in the graphic areas of the original was transmitted to the heat-sensitive layer of said element, causing the layer to become tackified in those areas corresponding to the printed character areas of the original.
  • the heat-sensitive element was separated from the graphic original and brushed with nigrosine dye as a developer.
  • Example 2 A heat-sensitive element was prepared as follows for use in a transfer process.
  • thermographic material was placed in contact with an original document so that the heat-sensitive layer of said material was in contact with the graphic portions of the original.
  • the 2-ply assembly was then exposed through the support side of said material.
  • the infrared exposing source was the same as that used in Example 1. The exposure produced tackey areas in said material corresponding to the image areas in the original. After exposure, the original and material of this example 'were separated.
  • the heat-sensitive element having tackiness in the image areas was then passed between pressure rollers exerting 30 pounds per linear inch of roller length and having a roller diameter of 2 /2 inches.
  • the coated side of the heat-sensitive element was in contact with a copy sheet of highly absorbent wet-strength paper.
  • the transfer produced good blue-black image reproduction of the original on the copy paper.
  • several high quality copies of the original were produced from the single thermographic exposure. The time which elapsed for the production of these several copies was approximately one minute.
  • Example 3 A heat-sensitive element was prepared as follows for use in preparing a lithographic printing plate.
  • a 10 percent solution of a heat-sensitive component, poly(2,2-dimethyltrimethylene succinate), said component having an inherent viscosity of 0.34 and a tackifying point of 79 C. was prepared in a 4:1 mixture of acetone and methylene chloride.
  • To the solution was added Azo Oil Blue Black B Dye at a concentration to give 5 percent (by weight) dye in the dry coated composition.
  • the composition was then coated by suitable means on to a parchment paper support. After the solvent was removed from the coating by drying, the element was annealed at 70 C. for 6 hours to give a final coating thickness of about 0.1 mil.
  • the heat-sensitive element was exposed as in Example 2, i.e., the heat-sensitive layer thereof was in contact with the printed characters of an original.
  • the infrared exposure produced tackified areas in the heat-sensitive layer of said element corresponding to the printed character areas of the original.
  • the exposed element was then passed between pressure rollers, as in Example 2, with the coated side of said element in contact with a hydrophilic-type paper support.
  • the lithographic plate was swabbed with a conventional plateconditioning solution and placed on an offset printing press. About 150 copies were run off on the press. Each of the 150 copies was of outstanding quality, exhibiting black letter outlines and good definition with substantially no background strain. There appeared to be substantially no deterioration in quality toward the end of the run of 150 copies.
  • Example 4 A heat-sensitive element of the present invention was prepared as follows for use in preparing a spirit duplicating master.
  • Example 1 A heat-sensitive element of Example 1 was exposed as in Example 2. After exposure and separation from the original, the heat-sensitive element was brushed lightly with powdered methyl violet dye as a developer. The tacky areas of the exposed element corresponding to the image areas of the original document picked up the colored developer and very good density and definition was obtained in the tacky areas. The resulting product was then used as a spirit duplicating master in a conventional process wherein a spirit duplicating copy paper, dampened with methanol, was brought into contact with the duplicating master with slight pressure applied, for example, with a handroller. A methyl violet reproduction of the original document was obtained in the copy paper. Several high quality copies of the original were obtained by repeating the process.
  • Example 5 To prepare a heat-sensitive element of the present invention, 8.5 grams of isotactic poly(butene- 1) having an inherent viscosity of 0.24 and a tackifying point of 96 C. was dissolved in 50 grams of methylene chloride containing 0.5 gram of Oil Black ST Dye and 0.5 gram of glass beads having an average diameter of about 18 to about 40 This mixture was then coated at a wet thickness of about 3 mils on a strip of Folio Transparent Copy Greaseproof Paper. After the solvent was removed from the coating by drying, the element was annealed for 18 hours at 75 C. The resulting heatsensitive element 'was exposed in contact with an original document as in Example 2.
  • the tacky areas produced in the heat-sensitive layer of said element resulting from the exposure were then pressed in contact with a paper copy sheet as in Example 2 to produce an excellent copy of the original. Several copies were obtained in like manner from a single exposure of the heat-sensitive element.
  • Example 6 To prepare a heat-sensitive element of the present invention 7.5 grams of a heat-sensitive component, poly(1,4-cyclohexanedimethyl adipate), said component having an inherent viscosity of 0.38 and a tackifying point of 92 C. were added to a solution comprising 2.5 grams of methyl violet dye in 5 grams of ethanol and 25 grams of ethylene chloride. The resulting composition was blended in a Waring Blendor for 5 minutes and then coated on a sheet of Folio Transparent Copy Greaseproof Paper with a doctor blade having a gap width of about 3 mils. After drying to remove the solvent from said coating, the element was annealed at 75 C. for 1 hour.
  • thermographic material was given bi-reflex exposure as described in Example 1 to produce tacky areas in the heat-sensitive layer of said element corresponding to the image areas of the original.
  • the heat-sensitive element having tackyagcas corresponding to the image areas of the original was then passed between pressure rollers with the coated side of said element in contact with a sheet of parchment copying paper.
  • the rollers for use in the transfer process had a roller diameter of 2 /2 inches and exerted pounds pressure per linear inch of roller length.
  • the resulting reverse-reading image was then used as a spirit duplicating master in a conventional process of this type wherein a spirit duplicating copy paper, dampened with methanol, was brought into contact with the master and subjected to slight pressure, for example, with a handroller. After pressure contacting, a methyl violet reproduction of the graphic original was obtained in the duplicating copy paper. By repeated transfer, approximately 25 copies of good quality were obtained from a single duplicating master.
  • Example 7 Another heat-sensitive element of the present invention for use in a transfer process was prepared by the addition of 95 grams of the condensation product of polymerized linoleic acid and a diamine (sold under the trade name Versamide 930 by General Mills), and 142 grams of benzoin acetate to 83 grams of isopropanol and 667 grams of benzene which contained 13 grams of Azo Oil Blue Black B Dye.
  • the polymer of said composition had a tackifying point in the range from to C. and the benzoin acetate had a melting point of about 82 C.
  • the composition was doctor blade coated on a sheet of Folio Transparent Copy Greaseproof Paper at a thickness of about 2 mils. The coating was then dried to eliminate the tacky state. The crystallized coating was next overcoated with a 2-mil wet thickness aqueous layer of 5 weight percent of polyvinyl alcohol containing less than 0.1 weight percent of an aryl sulfonate surfactant. The overcoated element was dried at about 50 C. for 10 minutes. The purpose of a protective overcoat was to stabilize the heatsensitive element and to facilitate packaging, thermographic exposure and transfer.
  • thermographic material was then exposed and a transfer to a paper copying sheet was made substantially as shown in Example 2 to produce a copy of the original having good quality, except that the receiver sheet was moistened with water prior to transfer and the rollers for use in the transfer process exerted 60 pounds pressure per lineal inch of roller length.
  • Example 8-A heat-sensitive element of the present invention with a rapid rate of crystallization was prepared as follows for use in the integrated rapid transfer unit of FIGURE 3.
  • thermographic material After annealing, the resulting thermographic material was placed in contact with an original document and the 2-ply assembly was then exposed and the tacky image areas were transferred rapidly to a third (receiving) sheet as shown in FIG. 3. The transfer operation was begun within 3 to 5 seconds after exposure and completed within the subsequent 5 to 7 seconds. A copy of excellent quality was obtained.
  • Example 9A heat-sensitive element of the present invention for use in a transfer process was prepared by coating onto Folio Transparent Copy Greaseproof Paper, a composition consisting of 9.0 grams of a heat-sensitive component, poly( 1,4 cyclohexanedimethylene adipateazelate [3:1]) having an inherent viscosity of 0.42 and a tackifying point of about 92 C., 1.0 gram of Isosol Black Dye, and 30 grams of ethylene chloride. After coating, the element was dried at 80 C. to yield a coating of 1.1 g./ft.
  • This heat-sensitive element was overcoated with a 2 /2 weight percent solution of medium viscosity carboxymethyl cellulose to form a protective overcoat, such as the one described in Example 7.
  • the overcoat was dried to yield a coating of 0.1 g./ft.
  • the resulting thermographic material was then exposed and a transfer to a paper copying sheet was made substantially as shown in Example 2 to produce a copy of the original having good quality, with the exception that the watersoluble overcoat required softening before transfer either by wiping the surface of the exposed matrix with a damp sponge or by dampening each receiving sheet.
  • a color-forming reaction can be employed, for example, where separate color-forming components of a two-component system are incorporated in each of separate polymeric layers, on a single support, or in separate polymeric layers on separate supports.
  • An example of a color-forming reaction of this type comprises, for example, incorporating ferric stearate in one layer and propyl gallate in a separate layer and thermographically exposing the supported layers in surface contact with a graphic original having infrared absorptive printed characters thereon.
  • a twocomponent color system of this type is also adapted to a multiple copy system where propyl gallate is incorporated in a receiving sheet and repeated transfers of a polymeric stratum containing ferric stearate is made to the receiving sheet from a matrix sheet.
  • Example 10 A heat-sensitive element of the present invention was prepared by the addition of 57 grams of the condensation product of polymerized linoleic acid and a diamine (sold under the trade name Versamide 930 by General Mills), 133 grams of bis(o-methoxyphenyl carbonate, 47 grams of n-dodecylamine and 12 grams of glass beads (IS-40a), to 51 grams of isopropanol and 700 grams of benzene.
  • the polymer of said composition had a tackifying point in the range from 105 to 115 C. and the bis(o-methoxyphenyl) carbonate had a melting point of about 87 C.
  • the resulting dispersion was coated on Folio Transparent Copy Greaseproof Paper. After coating, the element was air-dried for 4 hours to yield a colorless matrix.
  • the resulting colorless heat-sensitive element was exposed in contact with an originaldocument as described in Example 2.
  • the colorless tacky image areas produced in the heat-sensitive layer of said element resulting from the exposure were then pressed, under'60 pounds pressure per lineal inch of roller length, in contact with Diazo Paper 481 L, Blue Line ('Keuffel and Esser) as in Example 2, to produce a blue color reproduction of the original in the diazo paper receiving sheet.
  • Diazo Paper 481 L, Blue Line ('Keuffel and Esser) as in Example 2
  • the elements produced by the present invention are permanent in storage; and during use, the heat-sensitive layers thereof are unusually resistant to wear, abrasion, cracking, etc.
  • the processes in which the elements are employed are normally completely dry, thus not requiring chemicals, solvents, and the like.
  • the processes for copy reproduction normally do not require a final fixing or stabilizing step.
  • the copies produced by processes of the invention are permanent in that they are not aifected by high temperature and/or humidity conditions, etc. The copies are ideally suited as permanent file copies for this reason.
  • Calender rolls may be used to provide the necessary contact pressure. These rolls may be heated to a temperature in order to raise the temperature of the heat-sensitive element during transfer, thereby lowering the viscosity to a considerable extent in the activated image areas to facilitate transfer. Transfer can be effected by feeding the activated heat-sensitive element, and a receiving sheet in contact with the heatsensitive layer, through the nip of calender rolls.
  • the heat-sensitive element it is preferable to provide as a part of the heat-sensitive element some means for regulating transfer of viscous material from the activated portions of the heat-sensitive layer.
  • some means for regulating transfer is especially advantageous for improving transfer results. It prevents excessive flow of material to the receiving surface during the transfer step, thus conserving material in the matrix for producing more additional copies from a single heatsensitive element. Because the flow is attenuated while first copies are being made, heavier coats of sensitive material can be used without causing excessive transfer while making the first copies. Thus, with heavier heatsensitive coatings, even more copies are possible from a single heat-sensitive element.
  • the flow regulating means usually facilitates separation of the matrix from the transfer surface after the transfer step.
  • glass beads or other solid particles preferably of an average diameter or size slightly greater than the thickness of the heat-sensitive layer, when incorporated in the heat-sensitive layer will perform this flow regulating function. These solid particles preferably extend outward slightly from the heat-sensitive layer above the surface of the layer. Examples of heatsensitive layers containing glass beads are given in the foregoing examples.
  • An especially preferred flow regulating means that can be incorporated in the heat-sensitive element is a thin, porous, outer layer (non-thermoplastic at the tackifying temperature of the underlayer) on the heat-sensitive element, overlying the heat-sensitive layer.
  • This outer layer is sufficiently porous that at the contact pressures used for the transfer step, viscous material in the image area of the heat-sensitive layer can permeate the porous outer layer and be transferred to a receiving surface.
  • FIG. 4 is a schematic cutaway view of a heat-sensitive element having such a porous outer layer coated over an inner layer of heat-sensitive material on a support.
  • a heat-sensitive element having no fluid transfer regulating'means can be coated for use in a transfer process with a typical thermoplastic material to a maximum coating density of about 0.05 to about 0.3 gram per square foot. Heavier coatings would cause excessive transfer to first copies and consequent loss of image definition.
  • the melt viscosity of the heat-sensitive material preferably should be above 200 poises at the activation temperature. At room temperature an activated material having high viscosity characteristics can be transferred to a receiving sheet by calendering the heat-sensitive element in contact with a receiving sheet through steel rolls having a nip pressure of about 50 pounds per linear inch.
  • the maximum coating density can be increased.
  • the solid particles preferably extending outward above the heat-sensitive layer, will inhibit the flow of viscous material from the heat-sensitive layer.
  • Heat-sensitive materials having lower melt viscosity can be used and a contact pressure less than that required for the more viscous material can be used for the transfer step.
  • a preferred outer porous layer for regulating the flow of activated material from the heat-sensitive layer comprises a continuous porous Web of polyvinyl alcohol (PVA) overlying the heat-sensitive layer.
  • PVA polyvinyl alcohol
  • Such a web can be formed on the matrix by a solution coating method. Porosity and permeability of the web can be closely predetermined by regulating the coating conditions. When properly applied, the polyvinyl alcohol coating will form a porous permeable overcoat that provides excellent means for regulating fiow of viscous materials from the underlying heat-sensitive material.
  • the porosity of the web can be regulated to accommodate any of a wide variety of viscous transfer materials having a wide range of viscosity and flow characteristics.
  • a heat-sensitive layer of low melt viscosity material can be coated to maximum density of from about 1.5 up to about 3.0 grams per square foot without causing excessive transfer to first copies, and less transfer pressure is needed than for transfer of more viscous materials.
  • One important factor in forming the necessary porous structure in a polyvinyl alcohol coating is the presence in the coating solution of a pore-forming agent, either a metal salt or a surfactant, or in preferred embodiments both a salt and a surfactant.
  • a pore-forming agent either a metal salt or a surfactant, or in preferred embodiments both a salt and a surfactant.
  • Another step that sometimes improves the porous structure is the immediate heating of the matrix to a predetermined temperature as soon as the coating solution is applied over the heat-sensitive layer.
  • the flow regulating proper-ties of the polyvinyl alcohol can be improved for use in some embodiments by adding fine grain particles of solid material distributed throughout the porous outer layer. Coatings containing such added particles are especially advantageous for inhibiting flow of very low viscosity transfer materials.
  • F ollowi-ng is an example of preferred heat-sensitive element incorporating a porous polyvinyl alcohol overcoat.
  • Example 1 1.8.6 g. of a 25% solution of sodium su-lfate in water was stirred into 100 g. of a 5% solution of polyvinyl alcohol (Elvanol 5042) in water which contained 0.1 g. of a surfactant, Aerosol OT. 1.8 g. of zinc oxide was dispersed in the resulting solution using a food blendor. After the dispersion had defoamed, it was coated over a dyed heat-sensitive layer on a support of map overlay paper. The heat-sensitive layer comprised a 1.5 g./ft.
  • the transfers were made at a rate of 0.172 in./sec. using transfer rolls which were maintained at a temperature of 7075 C. and were loaded at 52 pounds per lineal inch.
  • the polyvinyl alcohol composition used in the above example is a commercially available aqueous solution of 87% hydrolyzed polyvinyl alcohol.
  • Other aqueous solutions of polyvinyl alcohol can be used, and solutions of PVA and other volatile surfactants, e.g., methanol, can be used, provided such other solvents will not attack the heat-sensitive layer during the coating process.
  • the total solids content of the coating solution, including PVA, salt, and insoluble particles is preferably in the range from about 5%9% by weight, based on the total weight of the solution. The remainder consists essentially of solvent.
  • Metal salts other than sodium sulfate which are soluble in the solvent medium can be substituted as pore-forming agents in the coating solution, for instance, such salts as Na PO Na2HPO4, KA1SO4, and NaC H O and the like, can be used.
  • Any of a wide variety of commercially available surface active agents can be used in the coating solution as web-forming agents, for example, Aerosol 22, sold by American Cyanamid Company, is especially suitable and a host of other surface active agents may be used.
  • Porous webs suitable as flow regulating means for heatsensitive elements have been formed from coating solutions containing from 10 to 60 parts by weight of salt per parts PVA, using no surfactant in the solution. However, presence of a surfactant up to a maximum of about 3% of .the weight of the coating solution will improve the porous structure for most embodiments.
  • a porous structure can be obtained by using only a surfactant without salt. However, the structure obtained using both a salt and a surfactant is preferred for most embodiments.
  • the temperature of the coating solution be raised above a certain minimum temperature immediately upon application of the coating solution over the heat-sensitive layer, and it is necessary that the temperature be held above this minimum until the porous structure has formed and the coating has substantially dried.
  • This minimum temperature which varies depending upon the composition of the solution will in most instances be in the range from about 35 to about 75 F. Without such immediate heating, the coating will dry as a nonporous film. Heating of the coating solution to this minimum temperature can be accomplished by applying the coating solution to the matrix while the matrix is in contact with a heated block or roll. Further heating to higher temperatures may be used to facilitate drying of the solvent from the coating, but with caution not to activate the heat-sensitive layer during high temperature drying.
  • Fine grain insoluble particles such as particles of zinc oxide
  • this coating has been applied and has dried as a porous layer, the fine grain particles will be evenly distributed throughout the porous web.
  • other fine grain materials suitable for this use are colloidal silica, titanium and zirconium dioxides, clays, and the like. For use in infrared processes, this material must be substantially infrared transparent. Fine grain insoluble particles are most effective when present in concentrations from about to 8 /2 by Weight based on the weight of PVA in the solution, and concentrations from 0 to 10% may be used.
  • the preferred coating density for the porous overcoating layer is in the range from about 0.3 to 0.7 gram per square foot, when dried. Below 0.2 gram per square foot density, the layer usually cannot provide adequate flow control. Coating densities for the porous outer layer up to about 1.0 gram per square foot (dry) may be used.
  • the porous outer layer may range in thickness from about 0.0001 inch to 0.002 inch thick and the individual openings may comprise from about to about 75% of the total area.
  • the openings are preferably evenly distributed over the matrix but some random fluctuation in distribution and size is permissible.
  • the optimum average size of the pores, or openings will vary depending on the viscosity of the heat-sensitive material and the conditions to be used for activation and transfer. Generally, optimum average pore size will range from about 0.1 micron .to about 500 microns and in most embodiments from about 1 to about microns.
  • porous outer layers may be used as flow regulating means.
  • thin films of cellulose esters, polyesters, polyamides, polycarbonates, thin metal foils and the like, that have been perforated or preformed to obtain the desired porosity and permeability, and then applied over the heatsensitive layer will function adequately in some embodiments.
  • porous papers, felted webs, and woven fabrics, having the necessary permeability and porosity requirements can be used as the porous outer layer for inhibiting flow of viscous material from the heat-sensitive layer in some embodiments.
  • Porous outer coatings for regulating flow of viscous material from the matrix may be used to advantage on matrices for use in other methods of document copying that embody the general principle of transferring viscous material from image areas of a matrix to a receiving surface.
  • the flow characteristics of whatever viscous fluid is being transferred can be regulated by the porous overlying layer to obtain the desired transfer characteristics.
  • a porous outer coating could be used to prevent excessive flow of melted Wax to the transfer surface.
  • the porous outer layer would be designed With the necessary porosity and permeability to permit permeation by only a desired amount of wax under prescribed process conditions.
  • porous overlying layer in which a porous overlying layer could be used to advantage are those for use in photographic diffusion transfer processes, image dye diffusion transfer processes, residual developer diffusion transfer processes, and photographic and thermographic colloid transfer processes. Some processes of these types are described in US. Patent No. 2,596,756, U.S. Patent 2,769,391 and 2,808,777.
  • a substantially infrared transparent heat-sensitive element for use in a thermographic process comprising in combination (A) a support,
  • thermoplastic material in a non-tacky state of at least partial crystallization and having an original tackifying temperature from 50 to 200 C. at which original tackifying temperature said thermoplastic material will undergo transition to an essentially non-crystalline state having a substantially lower tackifying temperature, said material having the property of remaining for a substantial period of time after said transition in a state having a reduced tackifying temperature substantially below said original tackifying temperature and having the property in such a state of being transferable by pressure at said reduced tackifying temperature, and
  • said porous outer layer comprising a continuous porous web of polyvinyl alcohol that has been coated over said heat-sensitive layer from a solution comprising parts by Weight of polyvinyl alcohol, from 10 to 60 parts by weight of a soluble metal salt and from 0 to 3 parts by weight of a surface-active agent.
  • a substantially infrared transparent heat-sensitive element for use in a thermographic process comprising in combination (A) a support,
  • thermoplastic material in a non-tacky state of at least partial crystallization and having an original tackifying temperature above 50 C. at which original tackifying temperature said thermoplastic material will undergo transition to an essentially non crystalline state having a substantially lower tackifying temperature, said material having the property of remaining for a substantial period of time after said transistion in a state having a reduced tackifying temperature substantially below said original tackifying temperaure and having the property in such state of being transferable by pressure at said reduced tackifying temperature, and
  • (C) means incorporated in said element for regulating transfer of tackified material from the heat-sensitive layer to a surface in contact with the heat-sensitive side of said element said means comprising solid inert particles having average diameter slightly greater than the thickess of said layer dispersed in said layer in a quantity sufficient to regulate said transfer.
  • thermoplastic 19 materal will undergo transition to an essentially noncrystalline state having a substantially reduced tackifying temperature, said material having the property of remaining for a substantial period of time after said transition in a state having a reduced tackifying temperature substantally below sad original tackifying temperature and having the property in such state of being transferable by pressure at a temperature above said reduced tackifying temperature and below said original tackifying temperature; said process comprising the steps of (l) preferentially heating only image areas on said heat-sensitive layer to at least said original tackifying temperature, and (2) after said preferential heating step and during said substantial period of time, with image areas and background areas of said heat-sensitve layer at a uniform temperature at least as high as said reduced tackifying temperature and below said original tackifying temperaure, pressing the heatsensitive side of the matrix at said areas of uniform temperature against a receivn-g surface wth pressure suificient to transfer tackified material from image areas of the heat sensitive layer to the
  • said heat-sensitive matrix sheet further comprises a dry, non-tacky, porous outer layer coated over said heat-sensitive layer, said porous outer layer being sufficiently permeable by said thermoplastic material in a viscous tacky state to permit limited transfer of such material in such state through said outer layer when the heat-sensitive side of the matrix is pressed against a receiving surface.
  • porous outer layer comprises a continuous porous Web of polyvinyl alcohol.
  • thermoplastic material consists essentially of a member selected from the group consisting of poly butene- 1), poly(pentene-l), poly(tert-butyl acrylate), poly(tetramethylene carbonate), poly(pentamethylene carbonate), oly(2,2-dinfethyltrirnethylene succinate), poly( 1,4-cyclohexanedimethylene succinate), poly(1,4-cyclohexanedimethylene adipate), poly(ethylene succinate), poly(.pentamethylene terephthalate), poly(ethylene 1,4-cyclohexanedicarboxylate), poly(ethylene glycol) and cyclohexanedimethylene adipate-azelate copolymers.
  • thermoplastic material consists essentially of a polymeric resin component intimately mixed with a non-polymeric crystalloid, which crystalloid will melt at an original tackifying temperature above 50 C. and upon melting will blend with said resin component to form a non-crystaline mixture that will remain for a substantial period in a state having a reduced tackifying temperature substantially below said original tackifying temperature.
  • thermoplastic material comprises a polymeric resin component which is at least partially crystallized in said layer and which at said original tackifying temperature will undergo transition to a substantially amorphous state having a second order transition temperature substantially below said original tackifying temperature.
  • said preferential heating step is accomplished by exposing to infrared radiation a graphic original having image areas that are infrared absorptive and background areas that are substantally infrared transparent while said original is in contact with the heat-sensitive matrix, for a time sufiicient to generate heat in the image areas of the original and thereby heat only the areas in the heat-sensitive matrix adjacent said image areas to at least said original tackifying temperature.
  • thermoplastic material at which original tackifying temperature said thermoplastic material will undergo transition to an essentially non-crystalline state having a substantially reduced tackifying temperature, said material having the property of remaining for a substantial period of time after said transition in a state having a reduced tackifying temperature and having the property in such state of being transferable by pressure at a temperature above said reduced tackifying temperature and below said original tackifying temperature, said process comprising the steps of (1) preferentially heating only image areas on said heat-sensitive layer to at least said original tackifying temperature, and (2) after said preferential heating step and during said sub stantial period of time, with image areas and background areas of said heat-sensitive layer at a uniform temperature at least as high as said reduced tackifying temperature and below said original tackifying temperature, pressing the heat-sensitive side of the matrix at said areas of uniform temperature against a receiving surface with pressure sufiicient to transfer tackified material from image areas of the heat-sensitive layer to the receiving surface, and (3) after such transfer of tackified material to the receiving
  • said preferential heating step is accomplished by exposing to infrared radiation a graphic original having image areas that are infrared absorptive and background areas that are substantially infrared transparent while said original is in contact with the heat-sensitive matrix, for a time sufficient to generate heat in the image areas of the original and thereby heat only the areas in the heat-sensitve matrix adjacent said image areas to at least said original tackifying temperature.
  • thermoplastic material at which original tackifying temperature said thermoplastic material will undergo transition to an essentially non-crystalline state having a substantially reduced tackifying temperature, said material having the property of remaining for a substantial period of time after said transition in a state having 2.1 a reduced tackifying temperature substantially below said original tackifying temperature and having the property in such a state of being transferable by pressure at a temperature above said reduced tackifying temperature and below said original tackifying temperature, said thermoplastic material having uniformly distributed therethrough a substantially infrared transparent color material, said process comprising the steps of (1) exposing to infrared radiation a graphic original having image areas that are infrared absorbent and background areas that are substantially infrared transparent, said orignal being in heat-conductive association with said heat-sensitive matrix for a time sufficient to generate heat in the image areas of said original and thereby to heat the areas in said heat-sensitive matrix adjacent said image areas to at least said original tackifying temperature, and (2) after said exposure and during said substantial period of time, with image areas

Landscapes

  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Power Engineering (AREA)
  • Architecture (AREA)
  • Structural Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Manufacturing & Machinery (AREA)
  • Thermal Transfer Or Thermal Recording In General (AREA)
  • Photosensitive Polymer And Photoresist Processing (AREA)
  • Printing Plates And Materials Therefor (AREA)
  • Developing Agents For Electrophotography (AREA)
US211927A 1961-07-14 1962-06-27 Thermographic recording process and heat-sensitive elements therefor Expired - Lifetime US3260612A (en)

Priority Applications (24)

Application Number Priority Date Filing Date Title
NL294592D NL294592A (de) 1961-07-14
FRJ8061696*8A FR95952E (de) 1961-07-14
NL294591D NL294591A (de) 1961-07-14
DE19621421406 DE1421406A1 (de) 1961-07-14 1962-06-01 Thermographisches Reproduktionsverfahren und thermographisches Kopiermaterial zur Durchfuehrung desselben
US211927A US3260612A (en) 1961-07-14 1962-06-27 Thermographic recording process and heat-sensitive elements therefor
FR903911A FR1472015A (fr) 1961-07-14 1962-07-13 Nouveaux produit et procédé thermosensibles pour la reproduction de documents
GB27283/62A GB1015925A (en) 1961-07-14 1962-07-16 Thermographic process and materials
GB23939/65A GB1015926A (en) 1961-07-14 1962-07-16 Thermographic process and materials
DK283863AA DK115123B (da) 1961-07-14 1963-06-14 Varmefølsomt kopieringsmateriale og fremgangsmåde til fremstilling af et porøst lag dertil.
DK283963A DK107814C (da) 1962-06-27 1963-06-14 Fremgangsmåde og materiale til termografisk kopiering af dokumenter.
AT789265A AT265019B (de) 1962-06-27 1963-06-17 Wärmeempfindliches Kopiermaterial für ein Trockenumdruckverfahren
AT662267A AT290295B (de) 1961-07-14 1963-06-17 Wärmeempfindliches Kopiermaterial für ein Trockenumdruckverfahren
AT485563A AT264552B (de) 1962-06-27 1963-06-17 Thermographisches Reproduktionsverfahren
DE19631471664 DE1471664A1 (de) 1961-07-14 1963-06-19 Thermographisches Reproduktionsverfahren und Material zur Durchfuehrung desselben
ES289370A ES289370A1 (es) 1962-06-27 1963-06-26 Método de copiar un documento
CH367666A CH449065A (fr) 1961-07-14 1963-06-27 Matériel thermosensible
CH793763A CH428804A (fr) 1961-07-14 1963-06-27 Procédé de copie thermographique
BE645645A BE645645A (de) 1961-07-14 1964-03-24
CH1022364A CH458412A (fr) 1961-07-14 1964-08-05 Procédé de copie thermographique par transfert à sec
US46335465 US3342623A (en) 1961-07-14 1965-06-11 Heat-sensitive elements for use in thermography
MY1966135A MY6600135A (en) 1961-07-14 1966-12-31 Thermographic process and materials
US614571A US3387974A (en) 1961-07-14 1967-02-08 Coatings for regulating transfer in photosensitive transfer elements
MY1969127A MY6900127A (en) 1961-07-14 1969-12-31 Thermographic process and materials
MY257/74A MY7400257A (en) 1961-07-14 1974-12-30 Thermographic process and materials

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US12403761A 1961-07-14 1961-07-14
US211927A US3260612A (en) 1961-07-14 1962-06-27 Thermographic recording process and heat-sensitive elements therefor
US614571A US3387974A (en) 1961-07-14 1967-02-08 Coatings for regulating transfer in photosensitive transfer elements

Publications (1)

Publication Number Publication Date
US3260612A true US3260612A (en) 1966-07-12

Family

ID=27383037

Family Applications (2)

Application Number Title Priority Date Filing Date
US211927A Expired - Lifetime US3260612A (en) 1961-07-14 1962-06-27 Thermographic recording process and heat-sensitive elements therefor
US614571A Expired - Lifetime US3387974A (en) 1961-07-14 1967-02-08 Coatings for regulating transfer in photosensitive transfer elements

Family Applications After (1)

Application Number Title Priority Date Filing Date
US614571A Expired - Lifetime US3387974A (en) 1961-07-14 1967-02-08 Coatings for regulating transfer in photosensitive transfer elements

Country Status (10)

Country Link
US (2) US3260612A (de)
AT (1) AT290295B (de)
BE (1) BE645645A (de)
CH (2) CH449065A (de)
DE (2) DE1421406A1 (de)
DK (1) DK115123B (de)
FR (1) FR95952E (de)
GB (2) GB1015926A (de)
MY (3) MY6600135A (de)
NL (2) NL294591A (de)

Cited By (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3342623A (en) * 1961-07-14 1967-09-19 Eastman Kodak Co Heat-sensitive elements for use in thermography
US3362380A (en) * 1964-10-08 1968-01-09 Minnesota Mining & Mfg Developer powder applicator unit having a supply roll with a magnetized working surface
US3364858A (en) * 1963-09-20 1968-01-23 Konishiroku Photo Ind Method for the preparation of an offset printing master
US3387974A (en) * 1961-07-14 1968-06-11 Eastman Kodak Co Coatings for regulating transfer in photosensitive transfer elements
US3395014A (en) * 1963-06-07 1968-07-30 Du Pont Preparation of printing plates by heat plus a pressure gradient
US3404994A (en) * 1965-02-11 1968-10-08 Arnold G. Gulko Thermographic copying process utilizing recording member with dispersed oil particles
US3442681A (en) * 1967-07-20 1969-05-06 Columbia Ribbon Carbon Mfg Transfer elements and method of making same
US3444809A (en) * 1965-06-05 1969-05-20 Fuji Photo Film Co Ltd Reproduction process
US3458335A (en) * 1967-02-14 1969-07-29 Columbia Ribbon Carbon Mfg Heat sensitive transfer sheet having screen layer and method of making
US3458336A (en) * 1967-02-14 1969-07-29 Columbia Ribbon Carbon Mfg Pressure sensitive transfer sheet having screen layer and method of making
US3463654A (en) * 1962-12-31 1969-08-26 Imagic Ltd Copying processes
US3473923A (en) * 1965-04-14 1969-10-21 Fuji Photo Film Co Ltd Reproduction process including transfer and redevelopment of electrostatically formed images
US3481761A (en) * 1967-03-15 1969-12-02 Columbia Ribbon Carbon Mfg Transfer elements and method of making same
US3491684A (en) * 1966-07-05 1970-01-27 Fallstaff Office Products Inc Unitary master and copy machine
US3493412A (en) * 1965-12-30 1970-02-03 Xerox Corp Transferring xerographic toner images to a solid crystalline plasticizer coated receiving surface
US3510336A (en) * 1965-08-12 1970-05-05 Gaf Great Britain Ltd Reflex copying method
US3515570A (en) * 1965-12-20 1970-06-02 Matsushita Electric Ind Co Ltd Heat-sensitive sheet and method of thermographic reproduction using the same
US3519464A (en) * 1967-03-01 1970-07-07 Ncr Co Master paper for thermal page printer
US3537872A (en) * 1963-02-26 1970-11-03 Hisako Kishida Thermographic process
US3632377A (en) * 1969-01-06 1972-01-04 Minnesota Mining & Mfg Image transfer sheet and method
US3637414A (en) * 1967-12-20 1972-01-25 Columbia Ribbon & Carbon Thermographic transfer sheet
US3715267A (en) * 1969-10-08 1973-02-06 Ricoh Kk Heat-sensitive stencil sheet
US3833441A (en) * 1962-10-24 1974-09-03 Du Pont Thermographic processes
US3902062A (en) * 1973-12-27 1975-08-26 Xerox Corp Reverse path imaging and transfixing copying method
US3904875A (en) * 1973-12-27 1975-09-09 Xerox Corp Single radiation ray path for thermographic imaging and transfixing or fusing
US3908125A (en) * 1973-12-27 1975-09-23 Xerox Corp Reverse path imaging and transfixing copying machine
US3941596A (en) * 1962-10-24 1976-03-02 E. I. Du Pont De Nemours And Company Thermographic processes using polymer layer capable of existing in metastable state
US3946230A (en) * 1973-12-27 1976-03-23 Xerox Corporation Copy method utilizing single radiant ray path for imaging and transfixing
US4007372A (en) * 1975-03-26 1977-02-08 Xerox Corporation Method and article for image reproduction
US4096294A (en) * 1977-04-04 1978-06-20 Xerox Corporation Process for preparing waterless printing masters comprising copolymer of siloxane and crystallized thermoplastic blocks
US4179532A (en) * 1976-04-09 1979-12-18 Polygram Gmbh Process for producing a disc-shaped information carrier which has information in the form of a beam-reflecting structure
US4263386A (en) * 1980-03-06 1981-04-21 Rca Corporation Method for the manufacture of multi-color microlithographic displays
US4263385A (en) * 1980-03-06 1981-04-21 Rca Corporation Method for the manufacture of multi-color microlithographic displays
EP0099731A2 (de) * 1982-07-16 1984-02-01 Minnesota Mining And Manufacturing Company Verfahren zur Erhaltung von permanenten Bildern
US4869996A (en) * 1987-12-18 1989-09-26 E. I. Du Pont De Nemours And Company Process for preparing negative images on a positive-type tonable photosensitive element
US4881084A (en) * 1986-07-25 1989-11-14 Canon Kabushiki Kaisha Image recording method using fluid ink electrochemically imparted with adhesiveness
US5039588A (en) * 1989-10-16 1991-08-13 E. I. Du Pont De Nemours And Company Non-electroscopic prolonged tack toners
US5049472A (en) * 1986-11-26 1991-09-17 Canon Kabushiki Kaisha Method and apparatus of recording image
WO1993008508A1 (en) * 1991-10-21 1993-04-29 Agfa-Gevaert Naamloze Vennootschap Method for producing images using a photopolymerizable composition
EP0522616B1 (de) * 1991-07-12 1995-10-04 Agfa-Gevaert N.V. Verfahren zur Herstellung von Bildern mittels einer photopolymerisierbaren Zusammensetzung
US5576074A (en) * 1995-08-23 1996-11-19 Minnesota Mining And Manufacturing Company Laser write process for making a conductive metal circuit
EP1472097B1 (de) * 2002-02-06 2007-09-12 E.I. Du Pont De Nemours And Company Bildübertragungselement, lasersystem, und verfahren zur herstellung von farbfilterelementen und flüssigkristallanzeigevorrichtungen
CN114929485A (zh) * 2020-01-08 2022-08-19 大日本印刷株式会社 剥离片、以及该剥离片与中间转印介质的组合

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3487764A (en) * 1966-12-14 1970-01-06 Eastman Kodak Co Photothermographic process and element
US4374691A (en) * 1980-05-09 1983-02-22 Minnesota Mining And Manufacturing Company Material and method for forming pressure transferable graphics
JPS57160691A (en) * 1981-03-31 1982-10-04 Fujitsu Ltd Ink composition for heat transfer recording and heat transfer recording ink sheet employing said composition
US4523207A (en) * 1983-03-30 1985-06-11 Ncr Corporation Multiple copy thermal record sheet
JPS60224590A (ja) * 1984-04-23 1985-11-08 Mitsubishi Chem Ind Ltd 昇華転写記録用シ−ト
US4732815A (en) * 1984-08-20 1988-03-22 Dai Nippon Insatsu Kabushiki Kaisha Heat transfer sheet
JPS6159448A (ja) * 1984-08-23 1986-03-26 ザ、ミード、コーポレーシヨン 改善された色調品質を有するカプセル化感放射線組成物を使用する感光画像形成材料
US4628000A (en) * 1984-12-28 1986-12-09 Ncr Corporation Thermal transfer formulation and medium
US4692395A (en) * 1986-01-29 1987-09-08 International Business Machines Corporation Transfer element and process for radiation defined images
US5108859A (en) * 1990-04-16 1992-04-28 Eastman Kodak Company Photoelectrographic elements and imaging method
DE4205713C2 (de) * 1992-02-25 1994-08-04 Siegwerk Druckfarben Gmbh & Co Druckfarbe, Verfahren zu ihrer Herstellung und deren Verwendung

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2462029A (en) * 1945-05-25 1949-02-15 Nashua Gummed & Coated Paper Adhesive compositions
US2503758A (en) * 1947-08-16 1950-04-11 Eastman Kodak Co Fusion photothermography
US2573881A (en) * 1948-11-02 1951-11-06 Battelle Development Corp Method and apparatus for developing electrostatic images with electroscopic powder
US2616961A (en) * 1946-09-23 1952-11-04 Groak Josef Printing
US2653880A (en) * 1949-09-15 1953-09-29 Minnesota Mining & Mfg Heat-activated temporarily pressure-sensitive adhesive tape
US2655453A (en) * 1952-04-23 1953-10-13 Ncr Co Manifold sheet having a crushresistant transfer film
US2678284A (en) * 1949-06-24 1954-05-11 Brown Bridge Mills Method of producing a thermoplastic adhesive and product thereof
GB722023A (en) * 1950-11-01 1955-01-19 Dick Co Ab Improvements in or relating to method for preparing copy
US2769391A (en) * 1951-11-14 1956-11-06 Dick Co Ab Method of manufacturing imaged hectograph spirit master
US2803579A (en) * 1954-09-01 1957-08-20 Buckeye Ribbon & Carbon Compan Method of making an impression medium
US2808777A (en) * 1952-02-26 1957-10-08 Dick Co Ab Method for manufacturing duplicating masters
US2954311A (en) * 1957-09-25 1960-09-27 Weel Walter H Vander Method for copying indicia by particle transfer
US2970534A (en) * 1952-03-27 1961-02-07 Dick Co Ab Planographic printing plates and methods for manufacturing same
US3060023A (en) * 1959-08-05 1962-10-23 Du Pont Image reproduction processes
US3080954A (en) * 1960-05-20 1963-03-12 Columbia Ribbon & Carbon Supercoated transfer elements
US3081699A (en) * 1958-12-22 1963-03-19 Arnold G Gulko Thermal reproduction

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL294592A (de) * 1961-07-14
BE625606A (de) * 1961-12-01

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2462029A (en) * 1945-05-25 1949-02-15 Nashua Gummed & Coated Paper Adhesive compositions
US2616961A (en) * 1946-09-23 1952-11-04 Groak Josef Printing
US2503758A (en) * 1947-08-16 1950-04-11 Eastman Kodak Co Fusion photothermography
US2573881A (en) * 1948-11-02 1951-11-06 Battelle Development Corp Method and apparatus for developing electrostatic images with electroscopic powder
US2678284A (en) * 1949-06-24 1954-05-11 Brown Bridge Mills Method of producing a thermoplastic adhesive and product thereof
US2653880A (en) * 1949-09-15 1953-09-29 Minnesota Mining & Mfg Heat-activated temporarily pressure-sensitive adhesive tape
GB722023A (en) * 1950-11-01 1955-01-19 Dick Co Ab Improvements in or relating to method for preparing copy
US2769391A (en) * 1951-11-14 1956-11-06 Dick Co Ab Method of manufacturing imaged hectograph spirit master
US2808777A (en) * 1952-02-26 1957-10-08 Dick Co Ab Method for manufacturing duplicating masters
US2970534A (en) * 1952-03-27 1961-02-07 Dick Co Ab Planographic printing plates and methods for manufacturing same
US2655453A (en) * 1952-04-23 1953-10-13 Ncr Co Manifold sheet having a crushresistant transfer film
US2803579A (en) * 1954-09-01 1957-08-20 Buckeye Ribbon & Carbon Compan Method of making an impression medium
US2954311A (en) * 1957-09-25 1960-09-27 Weel Walter H Vander Method for copying indicia by particle transfer
US3081699A (en) * 1958-12-22 1963-03-19 Arnold G Gulko Thermal reproduction
US3060023A (en) * 1959-08-05 1962-10-23 Du Pont Image reproduction processes
US3080954A (en) * 1960-05-20 1963-03-12 Columbia Ribbon & Carbon Supercoated transfer elements

Cited By (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3387974A (en) * 1961-07-14 1968-06-11 Eastman Kodak Co Coatings for regulating transfer in photosensitive transfer elements
US3342623A (en) * 1961-07-14 1967-09-19 Eastman Kodak Co Heat-sensitive elements for use in thermography
US3833441A (en) * 1962-10-24 1974-09-03 Du Pont Thermographic processes
US3941596A (en) * 1962-10-24 1976-03-02 E. I. Du Pont De Nemours And Company Thermographic processes using polymer layer capable of existing in metastable state
US3463654A (en) * 1962-12-31 1969-08-26 Imagic Ltd Copying processes
US3537872A (en) * 1963-02-26 1970-11-03 Hisako Kishida Thermographic process
US3395014A (en) * 1963-06-07 1968-07-30 Du Pont Preparation of printing plates by heat plus a pressure gradient
US3364858A (en) * 1963-09-20 1968-01-23 Konishiroku Photo Ind Method for the preparation of an offset printing master
US3362380A (en) * 1964-10-08 1968-01-09 Minnesota Mining & Mfg Developer powder applicator unit having a supply roll with a magnetized working surface
US3404994A (en) * 1965-02-11 1968-10-08 Arnold G. Gulko Thermographic copying process utilizing recording member with dispersed oil particles
US3473923A (en) * 1965-04-14 1969-10-21 Fuji Photo Film Co Ltd Reproduction process including transfer and redevelopment of electrostatically formed images
US3444809A (en) * 1965-06-05 1969-05-20 Fuji Photo Film Co Ltd Reproduction process
US3510336A (en) * 1965-08-12 1970-05-05 Gaf Great Britain Ltd Reflex copying method
US3515570A (en) * 1965-12-20 1970-06-02 Matsushita Electric Ind Co Ltd Heat-sensitive sheet and method of thermographic reproduction using the same
US3619279A (en) * 1965-12-30 1971-11-09 Xerox Corp Toner receiving member
US3493412A (en) * 1965-12-30 1970-02-03 Xerox Corp Transferring xerographic toner images to a solid crystalline plasticizer coated receiving surface
US3491684A (en) * 1966-07-05 1970-01-27 Fallstaff Office Products Inc Unitary master and copy machine
US3458335A (en) * 1967-02-14 1969-07-29 Columbia Ribbon Carbon Mfg Heat sensitive transfer sheet having screen layer and method of making
US3458336A (en) * 1967-02-14 1969-07-29 Columbia Ribbon Carbon Mfg Pressure sensitive transfer sheet having screen layer and method of making
US3519464A (en) * 1967-03-01 1970-07-07 Ncr Co Master paper for thermal page printer
US3519463A (en) * 1967-03-01 1970-07-07 Ncr Co Adhesive ink
US3481761A (en) * 1967-03-15 1969-12-02 Columbia Ribbon Carbon Mfg Transfer elements and method of making same
US3442681A (en) * 1967-07-20 1969-05-06 Columbia Ribbon Carbon Mfg Transfer elements and method of making same
US3637414A (en) * 1967-12-20 1972-01-25 Columbia Ribbon & Carbon Thermographic transfer sheet
US3632377A (en) * 1969-01-06 1972-01-04 Minnesota Mining & Mfg Image transfer sheet and method
US3715267A (en) * 1969-10-08 1973-02-06 Ricoh Kk Heat-sensitive stencil sheet
US3902062A (en) * 1973-12-27 1975-08-26 Xerox Corp Reverse path imaging and transfixing copying method
US3904875A (en) * 1973-12-27 1975-09-09 Xerox Corp Single radiation ray path for thermographic imaging and transfixing or fusing
US3908125A (en) * 1973-12-27 1975-09-23 Xerox Corp Reverse path imaging and transfixing copying machine
US3946230A (en) * 1973-12-27 1976-03-23 Xerox Corporation Copy method utilizing single radiant ray path for imaging and transfixing
US4007372A (en) * 1975-03-26 1977-02-08 Xerox Corporation Method and article for image reproduction
US4179532A (en) * 1976-04-09 1979-12-18 Polygram Gmbh Process for producing a disc-shaped information carrier which has information in the form of a beam-reflecting structure
US4096294A (en) * 1977-04-04 1978-06-20 Xerox Corporation Process for preparing waterless printing masters comprising copolymer of siloxane and crystallized thermoplastic blocks
US4263385A (en) * 1980-03-06 1981-04-21 Rca Corporation Method for the manufacture of multi-color microlithographic displays
US4263386A (en) * 1980-03-06 1981-04-21 Rca Corporation Method for the manufacture of multi-color microlithographic displays
EP0099731A2 (de) * 1982-07-16 1984-02-01 Minnesota Mining And Manufacturing Company Verfahren zur Erhaltung von permanenten Bildern
EP0099731A3 (en) * 1982-07-16 1985-11-27 Minnesota Mining And Manufacturing Company Improved method for providing permanent images
US4881084A (en) * 1986-07-25 1989-11-14 Canon Kabushiki Kaisha Image recording method using fluid ink electrochemically imparted with adhesiveness
US5049472A (en) * 1986-11-26 1991-09-17 Canon Kabushiki Kaisha Method and apparatus of recording image
US4869996A (en) * 1987-12-18 1989-09-26 E. I. Du Pont De Nemours And Company Process for preparing negative images on a positive-type tonable photosensitive element
US5039588A (en) * 1989-10-16 1991-08-13 E. I. Du Pont De Nemours And Company Non-electroscopic prolonged tack toners
EP0522616B1 (de) * 1991-07-12 1995-10-04 Agfa-Gevaert N.V. Verfahren zur Herstellung von Bildern mittels einer photopolymerisierbaren Zusammensetzung
WO1993008508A1 (en) * 1991-10-21 1993-04-29 Agfa-Gevaert Naamloze Vennootschap Method for producing images using a photopolymerizable composition
US5576074A (en) * 1995-08-23 1996-11-19 Minnesota Mining And Manufacturing Company Laser write process for making a conductive metal circuit
EP1472097B1 (de) * 2002-02-06 2007-09-12 E.I. Du Pont De Nemours And Company Bildübertragungselement, lasersystem, und verfahren zur herstellung von farbfilterelementen und flüssigkristallanzeigevorrichtungen
CN114929485A (zh) * 2020-01-08 2022-08-19 大日本印刷株式会社 剥离片、以及该剥离片与中间转印介质的组合

Also Published As

Publication number Publication date
CH449065A (fr) 1967-12-31
DE1471664A1 (de) 1970-04-16
DE1421406A1 (de) 1968-10-24
NL294592A (de)
MY6900127A (en) 1969-12-31
GB1015925A (en) 1966-01-05
DK115123B (da) 1969-09-08
BE645645A (de) 1964-09-24
CH428804A (fr) 1967-01-31
AT290295B (de) 1971-05-25
US3387974A (en) 1968-06-11
MY7400257A (en) 1974-12-31
NL294591A (de)
FR95952E (de) 1972-05-19
MY6600135A (en) 1966-12-31
GB1015926A (en) 1966-01-05

Similar Documents

Publication Publication Date Title
US3260612A (en) Thermographic recording process and heat-sensitive elements therefor
US2710263A (en) Heat-sensitive copying-paper
JPS6111293A (ja) 熱転写記録用受像シ−ト
US3149563A (en) Stencil-forming sheet material assembly
US3592644A (en) Thermorecording and reproduction of graphic information
US3795532A (en) Wide latitude copy sheet
US3922438A (en) Supercoated transfer elements and process for preparing and using same
DE4336164A1 (de) Thermisches Bildübertragungs-Aufzeichnungsmaterial
US3120611A (en) Method and apparatus for the negative reproduction of masters on a copy bearer utilizing a heat absorbing layer
US3852091A (en) Thermographic transfer sheets
US4411451A (en) Pressure sensitive copying paper
US3682684A (en) Wide latitude heat-sensitive copy-sheet and method of making
US3103881A (en) Method of copying
US3342623A (en) Heat-sensitive elements for use in thermography
US3539376A (en) Method of making copying paper
US3628979A (en) Transfer elements and method of making same
US3261023A (en) Thermographic recording process wherein the heat-sensitive sheet is used in plural processes
US3632377A (en) Image transfer sheet and method
JPS61228993A (ja) 熱溶融転写記録媒体
US3736873A (en) Planographic printing plate assembly and method of making
US5089371A (en) Heat development type diazo copying material containing a light insensitive intermediate layer provided between the support and the photosensitive layer
US3935362A (en) Image control means and structured transfer sheet for thermal reproduction processes
EP0060122B1 (de) Verfahren zur Herstellung von dauerhaften Bildern
JPS6122992A (ja) 熱転写記録シ−ト
US5976675A (en) Process for producing thermal transfer recording medium having near end mark