US3218168A - Heat and photosensitive copy sheet - Google Patents

Heat and photosensitive copy sheet Download PDF

Info

Publication number
US3218168A
US3218168A US230735A US23073562A US3218168A US 3218168 A US3218168 A US 3218168A US 230735 A US230735 A US 230735A US 23073562 A US23073562 A US 23073562A US 3218168 A US3218168 A US 3218168A
Authority
US
United States
Prior art keywords
sheet
copy
heat
coating
temperature
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
US230735A
Inventor
Wesley R Workman
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.)
3M Co
Original Assignee
Minnesota Mining and Manufacturing 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
Application filed by Minnesota Mining and Manufacturing Co filed Critical Minnesota Mining and Manufacturing Co
Priority to US230735A priority Critical patent/US3218168A/en
Priority to US490621A priority patent/US3282692A/en
Application granted granted Critical
Publication of US3218168A publication Critical patent/US3218168A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B13/00Preparation of cellulose ether-esters
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/494Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
    • G03C1/498Photothermographic systems, e.g. dry silver
    • G03C1/4989Photothermographic systems, e.g. dry silver characterised by a thermal imaging step, with or without exposure to light, e.g. with a thermal head, using a laser
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/027Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G03F7/028Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
    • G03F7/031Organic compounds not covered by group G03F7/029
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/038Macromolecular compounds which are rendered insoluble or differentially wettable
    • G03F7/0388Macromolecular compounds which are rendered insoluble or differentially wettable with ethylenic or acetylenic bands in the side chains of the photopolymer
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/039Macromolecular compounds which are photodegradable, e.g. positive electron resists

Definitions

  • This invention relates to the copying of graphic originals and has particular reference to visibly heat-sensitive copy-sheets useful for such purposes. lore particularly, the invention is concerned with visibly heat-sensitive copy-sheets capable of being desensitized by exposure to actinic radiation.
  • thermographic copying process One well-known and commercially important method of making copies of typewritten correspondence and like graphic originals is known as the thermographic copying process. As commonly employed, it involves brief irradiation of the differentially radiation-absorptive original, while in heat-conductive association with the copy- 7 sheet, with high-intensity radiation. Image areas of the copy-sheet corresponding to the thus preferentially heated radiation-absorptive inked image areas of the original are visibly changed. Background areas remain unchanged and still visibly heat-sensitive.
  • Heat-sensitive copy-sheets useful in thermographic copying processes and capable of undergoing permanent visible change when briefly heated to a conversion temperature within the commercially desirable range of about 60-150 C. are well known in the graphic arts. In some of these products the visible change results from chemical reaction of inter-reactive components maintained in intimate association with each other by a film-forming binder. In others the visible change occurs upon the clarification of an opalescent layer of particulate or discontinuous components, held in place by minor amounts of film-forming binder, into a continuous transparent covering through which a colored background may be seen.
  • thermographic copy-sheets are useful for retaining the reactive or fusible components in proper relationship and on the supporting backing. These binder materials are also helpful in preventing transfer of active materials to surfaces with which the copy-sheet comes in contact during the thermographic copying process. For such purposes it has generally been found desirable to employ polymers which do not fuse at the conversion temperature employed in thermocopying, such conversion temperature being normally Within the previously indicated comxerically desirable range of about 60150 C.
  • the present invention provides heat-sensitive copyshects of both the physical and chemical types which like the earlier types require only the brief application of a heat-image, e.g., by thermographic copying processes, to produce a visible copy, but which in addition may be stabilized against further heat-induced change at their original conversion temperature by simple irradiation with actinic light.
  • copy-sheets of the present invention may first be exposed to a desensitizing light pattern, for example through a stencil or a photographic transparency, and then subjected to uniform overall heating to cause a visible change only in the unexposed areas.
  • liquids, solutions, vapors, additional sheet ate materials, or other aids are not essential in producing accurate, legible, and fully stable copies of a wide variety of graphic originals.
  • thermographic copying practice with copysheets of the prior art fusion of the binder component of the chemically inter-reactive or particulate fusible heat-sensitive layers does not appear to occur, and binder components for thermographic heat-sensitive copy-sheet products are indeed normally selected as being non-fusing at temperatures attained in the copying process.
  • the visible change occurs as a result of localized softening of the binder itself or of a blend of binder and other constitutents, or as a result of local shrinkage or solubilizing or chemical change or other heat-induced alteration of the binder component, or solely through fusion or fiuidification of non-binder components, or by some other mechanism, is not known with certainty.
  • thermoplastic photosensitive film-forming materials in heat-sensitive copy-sheet structures as herein described has now resulted in copy-sheet products which are fully heat-sensitive as required in the thermographic copying process While being capable of desensitization against further heat-induced change.
  • Example 1 Visibly opaque heat-transparentizable coatings utilizing a photocrosslinkable polymer material provide useful stabilizable heat-sensitive copy-sheet products.
  • the coating is allowed to dry slowly under normal room conditions and subdued light, resulting in an opalescent blush layer which effectively conceals or masks much of the color of the underlying black paper carrier sheet.
  • the polyvinyl cinnamate is a yellowish thermoplastic film-forming photosensitive polymer material soluble in methyl ethyl ketone. It is commercially obtainable from Eastman Kodak Company at the filing date of this application as a 10% solution under the trademark Photo Resist. As thus obtained, the polyvinyl cinnamate polymer has a saponification value of about 168.
  • the dry polymer obtained in the form of small crumb-like particles by precipitation with water from the 10% solution followed by drying, has a softening range of about C., which may be raised to about -145 C. by a two-minute exposure of the water-precipitated dried crumb-like polymer to radiation from a BH6 high pressure mercury arc lamp held six inches away. This radiation is predominantly within the ultraviolet portion of the spectrum.
  • the softening point is conveniently determined on a Fisher-Johns melting point apparatus, the samples being placed between two thin microscope cover glasses and observed through a binocular microscope. A five-gram weight is placed upon the upper cover glass. The softening point is taken as that temperature at which the solid particle just begins to flow out. The rate of temperature rise is about one degree per minute, and in no case greater than three degrees per minute.
  • the opalescent blush layer transparentizes when the heat-sensitive copy-sheet is held in momentary contact with a metal test bar heated to 120 C., permitting the colored backing to beseen through the transparentized coating. The colored areas remain clearly visible on cooling.
  • Ultraviolet light is applied for two minutes through the onion-skin original from a BH-S lamp held six inches away.
  • Contacting the thus irradiated copy-sheet for a few seconds with a metal roller or platen heated to 130 C. selectively transparentizes the non-irradiated image portions of the opalescent coating to form a positive copy having black images on a light gray background.
  • the ultraviolet irradiated background areas do not transparentize when briefly subjected to test bar temperatures up to at least about 155 C.
  • Example 2 Desensitizable heat-sensitive transparentizable coatings may alternatively be applied to transparent backings to provide heat-sensitive copy-sheets which are particularly useful in preparing projection transparencies from differentially radiation-absorptive graphic originals.
  • a photocrosslinkable polymer material is first prepared as follows:
  • the photocrosslinkable thermoplastic film-forming polymer material thus obtained is dried in vacuo for two hours at room temperature and then for two hours at 40 C., under dark conditions. During the process the color changes from white to light tan.
  • the N-cinnamyl polypropanesultam thus obtained has a softening range of about 110115 C., and is about 70 percent alkylated. The softening range is raised to about 140l50 C. after a two-minute exposure to the ultraviolet radiation from a BH6 lamp held six inches away.
  • N-cinnamyl polypropane sultam is dissolved in ten parts dimethyl formamide.
  • the solution is applied at a thickness of four mils on a Z'mil Mylar tensilized polyester film backing and allowed to dry under room conditions and subdued light for approximately five minutes. While the coated side is still tacky to the touch, it is exposed briefly to a jet of steam whereupon the coating develops a semi-opaque non-tacky blush. Further drying results in a semi-opaque dried blush layer which is permanently transparentized when the coated sheet material is held in momentary contact with a metal test bar heated to 110 C.
  • the coated side of the sheet material is placed against the typewritten side of an opaque original and is frontprinted by brief exposure to intense radiation applied through the copy-sheet in a thermographic copying machine; a negative transparency is obtained, having clarified image areas and white opaque background areas which are still transparentizable when briefly heated to C.
  • Ultraviolet light from a BH6 lamp held six inches away is applied for two minutes onto the coated side of the imaged transparency.
  • the background areas thereafter remain opaque and will not transparentize when subjected to test bar temperatures as high as C.
  • the copy is effective as a projection transparency for use in overhead projectors.
  • Example 3 The two previous examples have utilized as the soluble, solid thermoplastic photosensitive film-forming material an unsaturated polymer that is in and of itself inherently photocrosslinkable and undergoes an increase in softening temperature under the influence of actinic radiation.
  • normally lightstable saturated polymers may similarly be made increasingly resistant to heat-softening under the influence of actinic radiation and thus the mixture may serve as a photosensitive material useful for the purposes of this invention.
  • One photoactivatible auxiliary component which is useful in the further polymerization of many normally light-stable saturated polymeric materials, is Z-methyl anthraquinone.
  • a solution is prepared consisting of:
  • Ethyl cellulose 100 Denatured ethanol 1900 Water 600
  • the N-200 ethyl cellulose is a white granular thermo- 1 plastic normally light-stable film-forming saturated polymer soluble in ketones and other solvents. It has a 47 /z49% ethoxy content, a softening range of 155170 C., and a viscosity of 200 cps. at 25 C. measured as a 5% solution in an 80:20 mixture of toluene and ethanol.
  • a portion of the above solution is spread in a thin layer on an inert smooth substrate and allowed to dry under room conditions and subdued light, resulting in a white readily pulverizable homogeneous residue.
  • the residue is removed from the substrate and pulverized by grinding with a mortar and pestle. It has a softening point of C.
  • Ultraviolet light from a BH6 lamp held six inches away is applied for two minutes onto the pulverized residue material.
  • the irradiated material has a softening point within the range of 185190 C. showing that the combination of ethyl cellulose and Z-methyl anthraquinone is effectively a photocrosslinkable filmforrning material.
  • Another portion of the solution is applied at a thickness of three mils on a 2-mil Mylar tensilized polyester film backing and allowed to dry slowly under room conditions and subdued light, resulting in an opalescent blush layer.
  • the coated sheet material is held in momentary contact with a metal test bar heated to 155, C., the opalescent blush layer transparentizes.
  • the coated side of the sheet material is placed against the typewritten side of an opaque original and is frontprinted by brief exposure of the differentially radiationabsorptive printed original to intense radiation applied through the copy-sheet in a thermographic copying machine; a negative transparency is obtained, having clarified image areas and white opaque background areas which are still transparentizable when briefly heated to 155 C.
  • Ultraviolet light from a BH6 lamp held six inches away is applied for two minutes onto the coated side of the imaged transparency.
  • the background areas thereafter remain opaque and will not transparentize when subjected to test bar temperatures as high as C.
  • opalescent blush layer is applied at a thickness of three mils on a similar 2-mil Mylar film backing and allowed to dry slowly under room conditions and subdued light, resulting in an opalescent blush layer.
  • the coated sheet material is held in momentary contact with a metal test bar heated to 155 C., the opalescent blush layer transparentizes.
  • thermographic sheet material The coated side of the thermographic sheet material is placed against the typewritten side of an opaque original and is front-printed by brief exposure to intense radiation in a thermographic copying machine; a negative transparency is obtained, having clarified image areas and white opaque background areas which are still transparentizable when briefly heated to 155 C.
  • Ultraviolet light from a BH-6 lamp held six inches away is applied for two minutes onto the coated side of the imaged transparency.
  • the background areas thereafter remain opaque and will not transparentize when subjected to test bar temperatures as high as 190 C., a 20 C. increase in irradiated background transparentization temperature over the sheet material previously described in this example.
  • the increased stability of the background toward heat is believed due to the particular efficiency of the photoactivatible auxiliary component herein employed, i.e., the acrylamides in admixture with 2- methyl anthraquinone.
  • the copy is similarly effective as a projection transparency for use in overhead projectors.
  • a further modification employs a solution consisting of:
  • the coated side of the film is placed against the typewritten side of an opaque original and is subjected to front-printing as previously described; a negative transparency is obtained, having clarified image areas and white opaque background areas which are still transparentizable when briefly heated to 115 C.
  • the photoactivatible auxiliary component herein employed i.e. the mixture of Z-m'ethyl anthraquinone and tetraethylene glycol dimethacrylate, has the unusual ability both to lower the transparentization temperature of the preirradiated sheet material and to increase the transparent- 6 ization temperature of the irradiated background areas.
  • the copy is eifective as a projection transparency for use in overhead projectors.
  • the copy-sheets of the present example may first be exposed to a desensitizing light pattern through a positive transparency, and then subjected to uniform overall heating to cause a visible change in the unexposed and still heat-sensitive background areas.
  • a desensitizing light pattern For example, the coated side of the sheet material initially produced in this example is placed against the typewritten side of a translucent onion-skin original, and ultraviolet light is applied for two minutes through the onion-skin orignial from a BH-6 lamp held six inches away.
  • a platen heated to 165 C. selectively transparentizes the non-irradiated image portions of the opalescent coating; the light-exposed background areas remain white and opaque.
  • Example 4 A solution of parts of polyethyl methacrylate having a softening point of 180 C., 20 parts of tetramethylene glycol dimethacrylate, and 6 parts of 2-methyl anthraquinone in acetone sufiicient to provide a concentration of 8% non-volatiles is coated on 2-mil Mylar polyester film at a coating orifice of 3 mils and dried under subdued light. Just prior to complete evaporation and while still tacky to the touch, the coating is exposed briefly to a jet of steam to develop a semi-opaque blush surface. The dried coating transparentizes when heated by brief contact with a metal test bar at C.
  • the coating is exposed through a photographic negative to the radiations from a BH-6 lamp at 6 inches for 2 minutes and is then briefly heated at -l40 C. to transparentize the unexposed areas, forming an effective projection transparency.
  • the exposed areas are capable of withstanding temperatures up to about 160 C. without transparentizing.
  • Example 5 A copy-sheet is prepared and tested as described in Example 4 except that the polyethyl methacrylate is replaced with an equal weight of copolymer of vinylidene chloride and acrylonitrile having a softening point of 200 C.
  • the opaque coating transparentizes at C. After irradiation the coating withstands temperatures up to about 200 C. After irradiation through the photographic negative transparency, development of the projection transparency is conveniently achieved by heating the sheet at 160 C.
  • Example 6 An eight percent solution in acetone of 100 parts of N-200 ethyl cellulose, 10 parts of thiourea. and 1.5 parts of rose bengal is coated at 3 mils on Mylar polyester film, dried, and opacified with steam as described in Example 4. The coating transparentizes on heating to C. The sheet is exposed through a photographic negative to radiation from a 500 watt tungsten filament projection lamp for eight minutes at an intensity of 10,000 foot candles and is then heated at C. whereupon a copy of the negative is obtained having transparent areas corresponding to the opaque areas of the negative. The opaque areas of the copy withstand temperatures up to about 170 C. before transparentizing.
  • the radiation from the projection lamp employed in this example is largely in the visible region.
  • Example 7 Mixtures of conventional binder materials with thermoplastic photocrosslinkable polymer materials provide effective transparentizable opaque heat-sensitive coatings and stabilizable heat-sensitive copy-sheets.
  • An improved copy-sheet construction is made by applying a thin color coating over the heat-transparentizable coating, and drying at room temperature.
  • the second coating serves to protect the heat-sensitive layer and to provide a visible color at image-forming transparentized areas when the copy is viewed through the transparent glassine paper. irradiation of the heat-transparentizable coating with ultraviolet through the glassine paper backing renders the normally heat-transparentizable background areas stable against further heating up to temperatures of at least 150 C.
  • the color coating is prepared by mixing together Parts Diane blue intra-red transmitting blue lake pigment 2 Ethyl cellulose 2 Commercial grade heptane ll Toluene 77 Glacial acetic acid 0.003
  • the coated side of the sheet material is placed against the typewritten side of an opaque original and the composite is subjected to front-printing in a thermographic copying machine; a positive copy is obtained, having blueappearing image areas and White opaque background areas which are still capable of assuming a colored appearance when briefiy heated to 110 C.
  • Ultraviolet light from a Bid-6 lamp held six inches away is applied for two minutes through the transparent film backing of the imaged copy-sheet.
  • the background areas thereafter remain white in appearance and do not convert to the blue appearance when subjected to test bar temperatures as high as 155 C.
  • An extremely thin and highly heat-sensitive modification of the copy-sheet of Example 7 is obtained by applying the coatings to a temporary carrier, such as a polished metal drum, from which the thin dried self-sustaining heatsensitive film product is subsequently removed by stripping.
  • a temporary carrier such as a polished metal drum
  • infra-redtransmitting colorants are required where front-printing with infra-red radiation is employed.
  • Example 8 Photocrosslinkable materials are effective in providing for the desensitization of normally heat-sensitive copysheet products which operate through the heat-induced localized physical oifsetting of colored materials.
  • a typewritten onion-skin paper original is placed with its reverse or unprinted side smoothly in contact with the wax-coated surface of the transfer sheet. Ultraviolet light from a Bil-6 lamp held six inches away is directed for two minutes through the onion-skin original onto the wax-coated surface.
  • the typewritten original is then replaced by a -lb. map overlay tracing paper receptor sheet, and the composite is subjected briefly to intense radiation in a thermographic copying machine. The two sheets are then separated. There is obtained a copy of the original consisting of blue images on the back surface of the receptor, and forming a right-reading copy as viewed through the transparent paper.
  • Three additional high contrast copies on separate sheets of the transparent receptor paper are similarly prepared tom the same transfer sheet.
  • the transfer sheet prepared in accordancewith this example provides copies of exceptionally clean background areas to thus increase overall copy contrast.
  • the photosensitive material may be present with one or another or both of the color-forming reactants to provide a heat-sensitive copy-sheet which is stabilizable by actinic irradiation.
  • a l-mil coating of a solution consisting of one part by weight ethyl cellulose, one part freshly prepared spiroindane, and ten parts methyl ethyl ketone is applied upon the first coating and the product is dried under subdued light at room temperature to provide a white heat-sensitive copy-sheet.
  • a graphic original typewritten on thin translucent onion-skin paper is placed smoothly in contact with the white copy-sheet prepared as just described and briefly exposed to intense radiant energy in accordance with the thermographic copying process, producing a copy of the original having blue-black letters on a white background.
  • Two identical copies are thus prepared.
  • the ultraviolet radiation of a BH-fi lamp held six inches away is applied for one minute to the imaged side of one of the copies.
  • the copies are then tested for sensitivity to heat.
  • the white background area of the ultraviolet exposed copy does not become visibly changed upon momentary contact with a metal test bar heated to 180 C. or to heat-images as conventionally developed during the thermographic copying process.
  • the white background area of the unexposed copy is visibly darkened immediately upon contact with a C. test bar.
  • Additional desensitized copies are prepared from the same thin translucent original by first exposing the white copy-sheet through the original to ultraviolet radiation of the intensity and duration previously described and then uniformly heating the selectivel irradiated copy-sheet to C.
  • a similarly useful copy-sheet is obtained by thoroughly mixing 30 parts of the silver soap dispersion with 14 parts of the spiroindane solution and coating the resultant mixture at a thickness of 3 mils onto 50-lb. basis weight opaque bond paper, and drying under subdued light at room temperature.
  • Example 1 illustrates the effectiveness of the photosensitive material in admixture with a conventional inert polymeric binder in a two-member desensitizable heatsensitive copy-sheet product of the chemically reactive type.
  • a graphic original typewritten on thin translucent onionskin paper is held smoothly in contact over the coated side of the image-sheet, and a portion of the sheet is selectively irradiated for one minute through the graphic original with the ultraviolet radiation of a BH-6 lamp held 6 inches away. The remaining portion of the twosheet combination is protected from the ultraviolet radiation with a suitable opaque shield.
  • a source sheet is provided by coating one-mil Mylar tensilized polyester film at 3 mils with a solution consisting of:
  • the coated side of the selectively irradiated imageshect is placed in heat-conductive contact with the coated side of the source sheet and the combination is held in contact with a metal platen heated to 140 C.
  • a highcontrast reproduction of the typewritten original appears on the irradiated portion of the White image sheet.
  • the non-irradiated protected portion becomes uniformly discolored with no evidence of discernible images thereon.
  • Image formation may alternatively be achieved by first heating a composite of source sheet and image sheet at image areas to obtain localized reaction and provide a visible copy, and then desensitizing the background areas of the image sheet by overall exposure to ultraviolet.
  • Example 11 In this example a photosensitive material is placed as a spacing or separating layer between layers of visibly inter-reactive chemical components in conventional inert polymeric binders in the preparation of a heat-sensitive copy-sheet which may subsequently be employed as an image transfer sheet in making further reproductions.
  • Ten parts by weight of a mixture of equal mol percent of silver behenate and behenic acid, one part of 1-(2H)- phthalazinone, three parts of Parapol S50L styreneisobutylene copolymer, and 86 parts of commercial grade heptane are ball-milled together for 16 hours to provide a uniform fine dispersion.
  • This dispersion is coated at a thickness of 1 mil onto a l-mil transparent Mylar tensilized polyester film backing, and dried.
  • a coating of a 20% solution of photosensitive polyvinyl cinnamate in methyl ethyl ketone is applied at a thickness of 1.5 mils over the first coating, and dried under conditions of subdued light.
  • a third coating is then applied at a thickness of 3 mils and consisting of a uniform mixture of 2 parts freshly prepared spiroindane, 2 parts of dithiooxamide, 4 parts of Siloid 244 finely powdered silicon dioxide, 7.4 parts Pliolite VT polyvinyl toluene resin, and 86 parts of commercial grade heptane.
  • the sheet is again dried under conditions of subdued light at room temperature to produce a heat-sensitive copy-sheet material which is desensitizable by actinic radiation.
  • the coated copy-sheet material is placed with its coated surface in contact with a graphic original of which a copy is desired, in this case an original typewritten on opaque paper, and the composite is subjected briefly to intense radiation rich in infra-red, applied through the sheet in accordance with therrnographic front-printing procedures.
  • a portion of the imaged surface of the copy is next irradiated for three minutes with ultraviolet light from a BH-6 high pressure mercury arc lamp held six inches away.
  • the remaining area is protected from the ultraviolet radiation with a suitable shield.
  • the protected background areas remain visibly heat-sensitive when briefiy subjected to a C. test bar; the irradiated background areas are found to be stabilized against visible change on brief contact with a test bar heated to C.
  • the copy thus formed has further utility in the preparation of additional reproductions on prepared receptor paper.
  • the imaged coated surface of the sheet is placed in contact with the coated surface of a receptor sheet consisting of SO-lb. basis white opaque bond paper having a coating of the dried residue of a l-mil layer of a ballrnilled mixture of 3 parts of nickel stearate, 2 parts of Siloid 244 silicon dioxide, 4 parts of Lemac 1000 polyvinyl acetate resin, and 46 parts of methyl ethyl ketone.
  • the composite is subjected to brief exposure to intense irradiation applied through the transparent film surface of the imaged copy-sheet and in accordance with the thermographic copying process, producing a further copy, in the form of black image areas against a clean white background, on the receptor sheet.
  • the letter images obtained from the ultraviolet treated and the non-treated areas of the copy-sheet are of identical high quality.
  • soluble solid thermoplastic photocrosslinkable polycondensation products of glycols such as decamethylene glycol
  • unsaturated dicarhoxylic acids such as cinnamylidenemalonic acid, crotonylidenemalonic acid, o-nitrocinnamylidenemalonic acid, naphthyl allylidenemalonic acid, and
  • N-methylquinolidene-Z-ethylidenemalonic acid the soluble solid thermoplastic photocrosslinkable reaction product of vinyl acetate and vinylazidophthalate with or without small proportions of vinyl alcohol residues; the soluble solid thermoplastic photocrosslinkable polymeric reaction products of acetophenone with styrene-maleic anhydridel-(betahydroxy ethoxyjbenzaldehyde or with methacrylic acid-4-(gammahydroxy propoxy)benzaldehyde intermediate products; the soluble solid thermoplastic photocrosslinkable polymeric reaction products of 4- hydroxyethoxy cinnamic acid with styrene-maleic anhydride copolymer; and the soluble solid thermoplastic photocrosslinkable polymeric reaction products of polyaminostyrene and cinnamoyl chloride.
  • the photosensitive material must be capable of retaining its initial physical form under normal storage and use conditions, must be susceptible of visible alteration, by appropriate modification of physical form, when briefly heated to a temperature within the range available in the thermoplastic copying process, and must be readily polymerized or cross-linked and rendered heat-resistant on exposure to actinic radiation.
  • fusible components such as particulate waxes or other light-diffusing materials are to be included, it'is ordinarily desirable to select particulate and polymeric materials having as nearly as possible the same refractive index and which in addition form non-crystallizing compatible blends.
  • a heat-sensitive copy-sheet product capable of undergoing permanent visible change on momentary contact with a heated metal test bar at a conversion temperature within the approximate range of 60 to 150 C. and of being stabilized against a said change on said contact by moderate exposure to actinic radiation, said product consisting of a composite of a source sheet and a receptor sheet component in face-to-face contact, said receptor sheet component including a surface layer comprising a normally solid organic acid salt of a noble metal, said source sheet component including a surface layer comprising an organic reducing agent for the noble metal ions, and at least one of said layers including a soluble solid thermoplastic photocrosslinkable organic film-forming polymer material which undergoes an increase in softening temperature of at least about 10 C.
  • the softening temperature being determined with the sample between cover-glasses under a weight of grams and under a uniform rate of temperature increase of 1-3 C. per minute.
  • a heat-sensitive copy-sheet consisting essentially of a strongly colored thin flexible paper backing and an optically discontinuous and non-transparent heat-transparentizable blushed coating of a soluble solid thermoplastic transparent photocrosslinkable organic film-forming polymer materials which undergoes an increase of at least about 10 C. irr softening temperature on exposure to actinic radiation from a BH6 high pressure mercury arc lamp at 6 inches for 2 minutes, the softening temperature being determined with the sample between cover glasses under a weight of 5 grams and under a uniform rate of temperature increase of l3 C. per minute.
  • a heat-sensitive copy-sheet consisting essentially of a transparent thin flexible backing and an optically discontinuous and non-transparent heat-transparentizable blushed coating of a soluble solid thermoplastic transparent photocrosslinkable organic film-forming polymer material which undergoes an increase of at least about 10 C. in softening temperature on exposure to actinic radiation from a Bil-6 hi h pressure mercury arc lamp at 6 inches for 2 minutes, the softening temperature being determined with the sample between cover glasses under a weight of 5 grams and under a uniform rate of temperature increase of l3 C. per minute.
  • a heat-sensitive copy-sheet consisting essentially of a thin flexible paper-like backing and a visibly heatsensitive chemically reactive coating capable on brief heating to a conversion temperature within the approximate range of to C. of converting to a permanently visibly distinct appearance by chemical reaction and capable of being rendered resistant to such action by moderate exposure to actinic radiation, said coating being further characterized as including a soluble solid thermoplastic photocrosslinkable organic film-forming polymeric binder material which undergoes an increase of at least about 10 C. in softening temperature on exposure to actinic radiation from a BH6 high pressure mercury arc lamp at 6 inches for 2 minutes, the softening temperature being determined with the sample between cover glasses under a weight of 5 grams andunder a uniform rate of temperature increase of 13 C. per minute.
  • a heat-sensitive copy-sheet consisting essentially of a thin flexible pa er-like backing and a visibly heatsensitive chemically reactive coating capable on brief heating to a conversion temperature within the approximate range of 60 to 150 C. of converting to a permanently visibly distinct appearance by chemical reaction and capable of being rendered resistant to such action by moderate exposure to actinic radiation, said coating comprising a uniform mixture of components consisting essentially of chemical co-reactants capable of undergoing visible co-reaction at said conversion temperature maintained in heat-reactive relationship by a soluble solid thermoplastic transparent photocrosslinkable organic filmforming polymeric binder material which undergoes an increase of at least about 10 C.
  • the softening temperature on exposure to actinic radiation from a Eli-6 high pressure mercury arc lamp at 6 inches for 2 minutes, the softening temperature being determined with the sample between cover glasses under a weight of 5 grams and under a uniform rate of temperature increase of 13 C. per minute.
  • a heat-sensitive copy-sheet consisting essentially of a thin flexible paper-like backing and a visibly heatsensitive chemically reactive coating capable on brief heating to a conversion temperature within the approximate range of 60 to 150 C. of converting to a permanently visibly distinct appearance by chemical reaction and capable of being rendered resistant to such action by moderate exposure to actinic radiation, said coating comprising in order a layer of a first chemical reactant material, a thin separating layer of a soluble solid thermoplastic photosensitive organic film-forming polymeric binder material which undergoes an increase in softening temperature of at least about C.
  • the softening temperature of the binder material being determined with the sample between cover glasses under a weight of 5 grams and under a uniform rate of temperature increase of 1-3" C. per minute.
  • a heat-sensitive copy-sheet consisting essentially of a thin flexible paper-like backing and a visibly heatsensitive chemically reactive coating capable on brief heating to a conversion temperature within the approximate range of 60 to 150 Ci of converting to a permanently visibly distinct appearance by chemical reaction and capable of being rendered resistant to such action by moderate exposure to actinic radiation, said coating comprising a normally solid organic acid salt of a noble metal ion, an organic reducing agent for said metal ion, and a soluble solid thermoplastic photosensitive organic film-forming polymeric binder material which undergoes an increase in softening temperature :of at least about 10 C. on exposure to actinic radiation from a BH-6 high pressure mercury arc lamp at 6 inches for 2 minutes, the softening temperature being determined with the sample between cover glasses under a weight of 5 grams and under a uniform rate of temperature increase of 13 C. per minute.

Description

3,218,168 HEAT AND PHOTOSENSITIVE COPY SHEET Wesley R. Workman, St. Paul, Minn., assignor to Minnesota Mining and Manufacturing Company, St. Paul, Minn., a corporation of Delaware N Drawing. Filed Oct. 15, 1962, Ser. No. 230,735 9 Claims. (Cl. 96-85) This invention relates to the copying of graphic originals and has particular reference to visibly heat-sensitive copy-sheets useful for such purposes. lore particularly, the invention is concerned with visibly heat-sensitive copy-sheets capable of being desensitized by exposure to actinic radiation.
One well-known and commercially important method of making copies of typewritten correspondence and like graphic originals is known as the thermographic copying process. As commonly employed, it involves brief irradiation of the differentially radiation-absorptive original, while in heat-conductive association with the copy- 7 sheet, with high-intensity radiation. Image areas of the copy-sheet corresponding to the thus preferentially heated radiation-absorptive inked image areas of the original are visibly changed. Background areas remain unchanged and still visibly heat-sensitive.
Heat-sensitive copy-sheets useful in thermographic copying processes and capable of undergoing permanent visible change when briefly heated to a conversion temperature within the commercially desirable range of about 60-150 C. are well known in the graphic arts. In some of these products the visible change results from chemical reaction of inter-reactive components maintained in intimate association with each other by a film-forming binder. In others the visible change occurs upon the clarification of an opalescent layer of particulate or discontinuous components, held in place by minor amounts of film-forming binder, into a continuous transparent covering through which a colored background may be seen.
The art has recognized that the film-forming binders employed in both the chemical and the physical type thermographic copy-sheets are useful for retaining the reactive or fusible components in proper relationship and on the supporting backing. These binder materials are also helpful in preventing transfer of active materials to surfaces with which the copy-sheet comes in contact during the thermographic copying process. For such purposes it has generally been found desirable to employ polymers which do not fuse at the conversion temperature employed in thermocopying, such conversion temperature being normally Within the previously indicated comxerically desirable range of about 60150 C.
While copies prepared on these heat-sensitive copysheets are stable and hence permanent under normal handling and storage, the still unchanged background areas obviously remain sensitive to further heating at the original conversion temperature within the stated approximate 60-150 C. range.
The present invention provides heat-sensitive copyshects of both the physical and chemical types which like the earlier types require only the brief application of a heat-image, e.g., by thermographic copying processes, to produce a visible copy, but which in addition may be stabilized against further heat-induced change at their original conversion temperature by simple irradiation with actinic light. Alternatively, copy-sheets of the present invention may first be exposed to a desensitizing light pattern, for example through a stencil or a photographic transparency, and then subjected to uniform overall heating to cause a visible change only in the unexposed areas. In either case, liquids, solutions, vapors, additional sheet ate materials, or other aids are not essential in producing accurate, legible, and fully stable copies of a wide variety of graphic originals.
Under thermographic copying practice with copysheets of the prior art, fusion of the binder component of the chemically inter-reactive or particulate fusible heat-sensitive layers does not appear to occur, and binder components for thermographic heat-sensitive copy-sheet products are indeed normally selected as being non-fusing at temperatures attained in the copying process. Whether the visible change occurs as a result of localized softening of the binder itself or of a blend of binder and other constitutents, or as a result of local shrinkage or solubilizing or chemical change or other heat-induced alteration of the binder component, or solely through fusion or fiuidification of non-binder components, or by some other mechanism, is not known with certainty. Unexpectedly, and regardless of theoretical mechanisms, the use of soluble, solid organic thermoplastic photosensitive film-forming materials in heat-sensitive copy-sheet structures as herein described has now resulted in copy-sheet products which are fully heat-sensitive as required in the thermographic copying process While being capable of desensitization against further heat-induced change.
The practice of the invention will now be described for convenience in terms of specific illustrative but nonlimiting examples in which proportions are designated as parts or percentages by weight.
Example 1 Visibly opaque heat-transparentizable coatings utilizing a photocrosslinkable polymer material provide useful stabilizable heat-sensitive copy-sheet products.
A solution consisting of Parts Polyvinyl cinnamate 10 Chloroform 298 Normal butanol 41 is applied at a thickness of five mils onto 50 lb. basis weight black radiation-absorptive cellulosic paper containing approximately one quarter its weight of carbon black and about 4% of a butadiene-styrene copolymer serving as a polymeric binder for the radiation-absorptive pigment. The coating is allowed to dry slowly under normal room conditions and subdued light, resulting in an opalescent blush layer which effectively conceals or masks much of the color of the underlying black paper carrier sheet.
The polyvinyl cinnamate is a yellowish thermoplastic film-forming photosensitive polymer material soluble in methyl ethyl ketone. It is commercially obtainable from Eastman Kodak Company at the filing date of this application as a 10% solution under the trademark Photo Resist. As thus obtained, the polyvinyl cinnamate polymer has a saponification value of about 168. The dry polymer, obtained in the form of small crumb-like particles by precipitation with water from the 10% solution followed by drying, has a softening range of about C., which may be raised to about -145 C. by a two-minute exposure of the water-precipitated dried crumb-like polymer to radiation from a BH6 high pressure mercury arc lamp held six inches away. This radiation is predominantly within the ultraviolet portion of the spectrum.
In this and similar cases the softening point is conveniently determined on a Fisher-Johns melting point apparatus, the samples being placed between two thin microscope cover glasses and observed through a binocular microscope. A five-gram weight is placed upon the upper cover glass. The softening point is taken as that temperature at which the solid particle just begins to flow out. The rate of temperature rise is about one degree per minute, and in no case greater than three degrees per minute.
The preparation of suitable polyvinyl cinnamate is described in British Patent 713,947. Essentially it comprises the esterification at moderately elevated temperature of highly saponified polyvinyl acetate in pyridine with cinnamoyl chloride added in small portions. The reaction product is extracted with methyl ethyl ketone, precipitated and washed with water, dried, and again dissolved to the desired consistency.
The opalescent blush layer transparentizes when the heat-sensitive copy-sheet is held in momentary contact with a metal test bar heated to 120 C., permitting the colored backing to beseen through the transparentized coating. The colored areas remain clearly visible on cooling.
A graphic original, typewritten on one side of trans lucent onion-skin paper, is placed smoothly upon the coated surface of the copy-sheet. Ultraviolet light is applied for two minutes through the onion-skin original from a BH-S lamp held six inches away. Contacting the thus irradiated copy-sheet for a few seconds with a metal roller or platen heated to 130 C. selectively transparentizes the non-irradiated image portions of the opalescent coating to form a positive copy having black images on a light gray background. The ultraviolet irradiated background areas do not transparentize when briefly subjected to test bar temperatures up to at least about 155 C.
Example 2 Desensitizable heat-sensitive transparentizable coatings may alternatively be applied to transparent backings to provide heat-sensitive copy-sheets which are particularly useful in preparing projection transparencies from differentially radiation-absorptive graphic originals.
A photocrosslinkable polymer material is first prepared as follows:
Twenty ml. of an aqueous solution containing 0.01 moles of the tetramethyl ammonium salt of polypropanesultam (formed from stoichiometric amounts of tetramethyl ammonium hydroxide and polypropane sultam) is heated to 80 C. while stirring, and to the hot solution is added 0.01 mole of cinnamyl chloride. The reaction mixture is maintained under mild agitation at 80 C. for minutes, whereupon the solution is made slightly acid by the controlled addition of concentrated hydrochloric acid. A rubbery mass of polymer thereupon separates' from the solution. The rubbery product is washed with water, ethanol and water, separately and in that order. The photocrosslinkable thermoplastic film-forming polymer material thus obtained is dried in vacuo for two hours at room temperature and then for two hours at 40 C., under dark conditions. During the process the color changes from white to light tan. The N-cinnamyl polypropanesultam thus obtained has a softening range of about 110115 C., and is about 70 percent alkylated. The softening range is raised to about 140l50 C. after a two-minute exposure to the ultraviolet radiation from a BH6 lamp held six inches away.
One part of the N-cinnamyl polypropane sultam is dissolved in ten parts dimethyl formamide. The solution is applied at a thickness of four mils on a Z'mil Mylar tensilized polyester film backing and allowed to dry under room conditions and subdued light for approximately five minutes. While the coated side is still tacky to the touch, it is exposed briefly to a jet of steam whereupon the coating develops a semi-opaque non-tacky blush. Further drying results in a semi-opaque dried blush layer which is permanently transparentized when the coated sheet material is held in momentary contact with a metal test bar heated to 110 C.
The coated side of the sheet material is placed against the typewritten side of an opaque original and is frontprinted by brief exposure to intense radiation applied through the copy-sheet in a thermographic copying machine; a negative transparency is obtained, having clarified image areas and white opaque background areas which are still transparentizable when briefly heated to C.
Ultraviolet light from a BH6 lamp held six inches away is applied for two minutes onto the coated side of the imaged transparency. The background areas thereafter remain opaque and will not transparentize when subjected to test bar temperatures as high as C. The copy is effective as a projection transparency for use in overhead projectors.
Example 3 The two previous examples have utilized as the soluble, solid thermoplastic photosensitive film-forming material an unsaturated polymer that is in and of itself inherently photocrosslinkable and undergoes an increase in softening temperature under the influence of actinic radiation.
However, when a photoactivatible auxiliary component is employed in conjunction therewith, normally lightstable saturated polymers may similarly be made increasingly resistant to heat-softening under the influence of actinic radiation and thus the mixture may serve as a photosensitive material useful for the purposes of this invention. One photoactivatible auxiliary component, which is useful in the further polymerization of many normally light-stable saturated polymeric materials, is Z-methyl anthraquinone.
A solution is prepared consisting of:
Parts 2-methyl anthraquinone 6 Ethyl cellulose (N200) 100 Denatured ethanol 1900 Water 600 The N-200 ethyl cellulose is a white granular thermo- 1 plastic normally light-stable film-forming saturated polymer soluble in ketones and other solvents. It has a 47 /z49% ethoxy content, a softening range of 155170 C., and a viscosity of 200 cps. at 25 C. measured as a 5% solution in an 80:20 mixture of toluene and ethanol.
A portion of the above solution is spread in a thin layer on an inert smooth substrate and allowed to dry under room conditions and subdued light, resulting in a white readily pulverizable homogeneous residue. The residue is removed from the substrate and pulverized by grinding with a mortar and pestle. It has a softening point of C. Ultraviolet light from a BH6 lamp held six inches away is applied for two minutes onto the pulverized residue material. The irradiated material has a softening point within the range of 185190 C. showing that the combination of ethyl cellulose and Z-methyl anthraquinone is effectively a photocrosslinkable filmforrning material.
Another portion of the solution is applied at a thickness of three mils on a 2-mil Mylar tensilized polyester film backing and allowed to dry slowly under room conditions and subdued light, resulting in an opalescent blush layer. When the coated sheet material is held in momentary contact with a metal test bar heated to 155, C., the opalescent blush layer transparentizes.
The coated side of the sheet material is placed against the typewritten side of an opaque original and is frontprinted by brief exposure of the differentially radiationabsorptive printed original to intense radiation applied through the copy-sheet in a thermographic copying machine; a negative transparency is obtained, having clarified image areas and white opaque background areas which are still transparentizable when briefly heated to 155 C.
Ultraviolet light from a BH6 lamp held six inches away is applied for two minutes onto the coated side of the imaged transparency. The background areas thereafter remain opaque and will not transparentize when subjected to test bar temperatures as high as C. The
copy is effective as a projection transparency for use in overhead projectors.
In a modification of the foregoing copy-sheet, a solution consisting of:
is applied at a thickness of three mils on a similar 2-mil Mylar film backing and allowed to dry slowly under room conditions and subdued light, resulting in an opalescent blush layer. When the coated sheet material is held in momentary contact with a metal test bar heated to 155 C., the opalescent blush layer transparentizes.
The coated side of the thermographic sheet material is placed against the typewritten side of an opaque original and is front-printed by brief exposure to intense radiation in a thermographic copying machine; a negative transparency is obtained, having clarified image areas and white opaque background areas which are still transparentizable when briefly heated to 155 C.
Ultraviolet light from a BH-6 lamp held six inches away is applied for two minutes onto the coated side of the imaged transparency. The background areas thereafter remain opaque and will not transparentize when subjected to test bar temperatures as high as 190 C., a 20 C. increase in irradiated background transparentization temperature over the sheet material previously described in this example. The increased stability of the background toward heat is believed due to the particular efficiency of the photoactivatible auxiliary component herein employed, i.e., the acrylamides in admixture with 2- methyl anthraquinone. The copy is similarly effective as a projection transparency for use in overhead projectors.
A further modification employs a solution consisting of:
Parts Z-methyl anthraquinone 6 Ethyl cellulose (N200) 100 Tetraethylene glycol dimethacrylate 20 Denatured ethanol 1900 Water 600 The solution is applied at a thickness of three mils on a Z-mil Mylar polyester film backing and allowed to dry slowly under room conditions and subdued light, resulting in an opalescent blush layer. The coating transparentizes when the sheet is placed in contact with a metal test bar at 115 C., i.e. to a temperature some 40 C. lower than is required to transparentize the coating prepared of ethyl cellulose in the absence of the tetraethylene glycol dimethacrylate.
The coated side of the film is placed against the typewritten side of an opaque original and is subjected to front-printing as previously described; a negative transparency is obtained, having clarified image areas and white opaque background areas which are still transparentizable when briefly heated to 115 C.
Ultraviolet light from a BH-6 lamp held six inches away is applied for two minutes onto the coated side of the imaged transparency. The background areas thereafter remain opaque and will not transparentize when subjected to test bar temperatures as high as 190 C., again a 20 C. increase in the transparentization temperature of the irradiated background areas over the initially produced sheet material of this example. Thus, the photoactivatible auxiliary component herein employed i.e. the mixture of Z-m'ethyl anthraquinone and tetraethylene glycol dimethacrylate, has the unusual ability both to lower the transparentization temperature of the preirradiated sheet material and to increase the transparent- 6 ization temperature of the irradiated background areas. The copy is eifective as a projection transparency for use in overhead projectors.
Alternatively, the copy-sheets of the present example may first be exposed to a desensitizing light pattern through a positive transparency, and then subjected to uniform overall heating to cause a visible change in the unexposed and still heat-sensitive background areas. For example, the coated side of the sheet material initially produced in this example is placed against the typewritten side of a translucent onion-skin original, and ultraviolet light is applied for two minutes through the onion-skin orignial from a BH-6 lamp held six inches away. Contacting the thus irradiated sheet material for a few seconds with a platen heated to 165 C. selectively transparentizes the non-irradiated image portions of the opalescent coating; the light-exposed background areas remain white and opaque.
Example 4 A solution of parts of polyethyl methacrylate having a softening point of 180 C., 20 parts of tetramethylene glycol dimethacrylate, and 6 parts of 2-methyl anthraquinone in acetone sufiicient to provide a concentration of 8% non-volatiles is coated on 2-mil Mylar polyester film at a coating orifice of 3 mils and dried under subdued light. Just prior to complete evaporation and while still tacky to the touch, the coating is exposed briefly to a jet of steam to develop a semi-opaque blush surface. The dried coating transparentizes when heated by brief contact with a metal test bar at C. The coating is exposed through a photographic negative to the radiations from a BH-6 lamp at 6 inches for 2 minutes and is then briefly heated at -l40 C. to transparentize the unexposed areas, forming an effective projection transparency. The exposed areas are capable of withstanding temperatures up to about 160 C. without transparentizing.
Example 5 A copy-sheet is prepared and tested as described in Example 4 except that the polyethyl methacrylate is replaced with an equal weight of copolymer of vinylidene chloride and acrylonitrile having a softening point of 200 C. The opaque coating transparentizes at C. After irradiation the coating withstands temperatures up to about 200 C. After irradiation through the photographic negative transparency, development of the projection transparency is conveniently achieved by heating the sheet at 160 C.
Example 6 An eight percent solution in acetone of 100 parts of N-200 ethyl cellulose, 10 parts of thiourea. and 1.5 parts of rose bengal is coated at 3 mils on Mylar polyester film, dried, and opacified with steam as described in Example 4. The coating transparentizes on heating to C. The sheet is exposed through a photographic negative to radiation from a 500 watt tungsten filament projection lamp for eight minutes at an intensity of 10,000 foot candles and is then heated at C. whereupon a copy of the negative is obtained having transparent areas corresponding to the opaque areas of the negative. The opaque areas of the copy withstand temperatures up to about 170 C. before transparentizing.
The radiation from the projection lamp employed in this example is largely in the visible region.
Example 7 Mixtures of conventional binder materials with thermoplastic photocrosslinkable polymer materials provide effective transparentizable opaque heat-sensitive coatings and stabilizable heat-sensitive copy-sheets.
A solution consisting of:
Parts Polyvinyl cinnamate 10 Polymethyl methacrylate Acryloid Kl20 10 Butyl stearate 1 Methyl ethyl ketone 380 aarsnss is applied at a thickness of four mils onto 25-lb. transparent glassine paper and dried at room temperature. The resultant coating is substantially opaque, The coated sheet is adaptable for tront-printing in a thermographic copying machine to provide a copy of a graphic original in the form of a positive transparency having light-scattering white-appearing background areas. The nearly opaque background clarifies when held in momentary contact with a 125 C. test bar. Exposure to ultraviolet radiation as described in Example 1 increases the temperature requirement for transparentization to at least about 150 C.
An improved copy-sheet construction is made by applying a thin color coating over the heat-transparentizable coating, and drying at room temperature. The second coating serves to protect the heat-sensitive layer and to provide a visible color at image-forming transparentized areas when the copy is viewed through the transparent glassine paper. irradiation of the heat-transparentizable coating with ultraviolet through the glassine paper backing renders the normally heat-transparentizable background areas stable against further heating up to temperatures of at least 150 C.
The color coating is prepared by mixing together Parts Diane blue intra-red transmitting blue lake pigment 2 Ethyl cellulose 2 Commercial grade heptane ll Toluene 77 Glacial acetic acid 0.003
The coated side of the sheet material is placed against the typewritten side of an opaque original and the composite is subjected to front-printing in a thermographic copying machine; a positive copy is obtained, having blueappearing image areas and White opaque background areas which are still capable of assuming a colored appearance when briefiy heated to 110 C.
Ultraviolet light from a Bid-6 lamp held six inches away is applied for two minutes through the transparent film backing of the imaged copy-sheet. The background areas thereafter remain white in appearance and do not convert to the blue appearance when subjected to test bar temperatures as high as 155 C.
An extremely thin and highly heat-sensitive modification of the copy-sheet of Example 7 is obtained by applying the coatings to a temporary carrier, such as a polished metal drum, from which the thin dried self-sustaining heatsensitive film product is subsequently removed by stripping.
Other pigments, dyes or other coloring agents may be used in place of the specific pigment named. infra-redtransmitting colorants are required where front-printing with infra-red radiation is employed.
Example 8 Photocrosslinkable materials are effective in providing for the desensitization of normally heat-sensitive copysheet products which operate through the heat-induced localized physical oifsetting of colored materials.
The following mixture consisting of:
Polyvinyl cinnamate Castor wax Triphenyl phosphate 4 Diane Blue pigment 1 Methyl ethyl ketone u Methanol 10 translucent durable blue coating on the black radiationabsorptive backing provides a transfer sheet.
A typewritten onion-skin paper original is placed with its reverse or unprinted side smoothly in contact with the wax-coated surface of the transfer sheet. Ultraviolet light from a Bil-6 lamp held six inches away is directed for two minutes through the onion-skin original onto the wax-coated surface. The typewritten original is then replaced by a -lb. map overlay tracing paper receptor sheet, and the composite is subjected briefly to intense radiation in a thermographic copying machine. The two sheets are then separated. There is obtained a copy of the original consisting of blue images on the back surface of the receptor, and forming a right-reading copy as viewed through the transparent paper. Three additional high contrast copies on separate sheets of the transparent receptor paper are similarly prepared tom the same transfer sheet.
The transfer sheet prepared in accordancewith this example provides copies of exceptionally clean background areas to thus increase overall copy contrast.
Other visually transparent or translucent flexible heatresistant receptor sheets, e.g., thin paper, cellulosic films, vinyl films and the like are similarly useful.
With ethyl cellulose, polyvinyl toluene, polymethyl methacrylate or other conventional inert binder materials substituted for the polyvinyl cinnamate photosensitive material in the wax coating of the transfer sheet, under.
the copying procedure just described, no copy of the typewritten original results; instead, the entire surface of the wax coating transfers to the receptor.
Example 9 In the chemical type copy-sheet the photosensitive material may be present with one or another or both of the color-forming reactants to provide a heat-sensitive copy-sheet which is stabilizable by actinic irradiation.
Twenty-five parts by weight of a mixture of equal mol percent of silver behenate and behenic acid, forty-five parts of polyvinyl cinnamate as described in Example 1, two and one-half parts of 1-(2l-l)-phthalazinone and five hundred parts of methyl ethyl ketone are ball-milled together for 16 hours to provide a uniform finedispersion. This dispersion is coated at a thickness of 2 mils onto lb. basis weight opaque bond paper, and dried in subdued light. A l-mil coating of a solution consisting of one part by weight ethyl cellulose, one part freshly prepared spiroindane, and ten parts methyl ethyl ketone is applied upon the first coating and the product is dried under subdued light at room temperature to provide a white heat-sensitive copy-sheet.
A graphic original typewritten on thin translucent onion-skin paper is placed smoothly in contact with the white copy-sheet prepared as just described and briefly exposed to intense radiant energy in accordance with the thermographic copying process, producing a copy of the original having blue-black letters on a white background. Two identical copies are thus prepared. The ultraviolet radiation of a BH-fi lamp held six inches away is applied for one minute to the imaged side of one of the copies. The copies are then tested for sensitivity to heat. The white background area of the ultraviolet exposed copy does not become visibly changed upon momentary contact with a metal test bar heated to 180 C. or to heat-images as conventionally developed during the thermographic copying process. However, the white background area of the unexposed copy is visibly darkened immediately upon contact with a C. test bar.
Additional desensitized copies are prepared from the same thin translucent original by first exposing the white copy-sheet through the original to ultraviolet radiation of the intensity and duration previously described and then uniformly heating the selectivel irradiated copy-sheet to C.
A similarly useful copy-sheet is obtained by thoroughly mixing 30 parts of the silver soap dispersion with 14 parts of the spiroindane solution and coating the resultant mixture at a thickness of 3 mils onto 50-lb. basis weight opaque bond paper, and drying under subdued light at room temperature.
Analogous results are obtained by repeating this entire example with nickel stearate, stearic acid and dibenzyl dithiooxamide substituted for the silver behenate, behenic acid and spiroindane, respectively.
Example This example illustrates the effectiveness of the photosensitive material in admixture with a conventional inert polymeric binder in a two-member desensitizable heatsensitive copy-sheet product of the chemically reactive type.
Six parts by weight of a mixture of equal mol percent of silver behenate and behenic acid is dispersed in a solution of four parts of polystyrene resin in fifty parts ethyl acetate by grinding in a ball mill for 16 hours to provide a uniform and very fine dispersion. This dispersion is coated at a thickness of 2 mils onto 50-lb. basis weight opaque bond paper and dried. A coating consisting of one part polyvinyl cinnamate, one part polyvinyl toluene, and four parts methyl ethyl ketone is applied at a thickness of one mil over the first coating and dried in subdued light to complete the preparation of a white receptor or image-sheet.
A graphic original typewritten on thin translucent onionskin paper is held smoothly in contact over the coated side of the image-sheet, and a portion of the sheet is selectively irradiated for one minute through the graphic original with the ultraviolet radiation of a BH-6 lamp held 6 inches away. The remaining portion of the twosheet combination is protected from the ultraviolet radiation with a suitable opaque shield.
A source sheet is provided by coating one-mil Mylar tensilized polyester film at 3 mils with a solution consisting of:
Parts 4-methoxy-l-hydroxy naphthalene 10 Ethyl cellulose 40 Methyl ethyl ketone 350 The coating is dried in subdued light at room temperaturc.
The coated side of the selectively irradiated imageshect is placed in heat-conductive contact with the coated side of the source sheet and the combination is held in contact with a metal platen heated to 140 C. A highcontrast reproduction of the typewritten original appears on the irradiated portion of the White image sheet. The non-irradiated protected portion becomes uniformly discolored with no evidence of discernible images thereon.
Image formation may alternatively be achieved by first heating a composite of source sheet and image sheet at image areas to obtain localized reaction and provide a visible copy, and then desensitizing the background areas of the image sheet by overall exposure to ultraviolet.
Example 11 In this example a photosensitive material is placed as a spacing or separating layer between layers of visibly inter-reactive chemical components in conventional inert polymeric binders in the preparation of a heat-sensitive copy-sheet which may subsequently be employed as an image transfer sheet in making further reproductions.
Ten parts by weight of a mixture of equal mol percent of silver behenate and behenic acid, one part of 1-(2H)- phthalazinone, three parts of Parapol S50L styreneisobutylene copolymer, and 86 parts of commercial grade heptane are ball-milled together for 16 hours to provide a uniform fine dispersion. This dispersion is coated at a thickness of 1 mil onto a l-mil transparent Mylar tensilized polyester film backing, and dried. A coating of a 20% solution of photosensitive polyvinyl cinnamate in methyl ethyl ketone is applied at a thickness of 1.5 mils over the first coating, and dried under conditions of subdued light. A third coating is then applied at a thickness of 3 mils and consisting of a uniform mixture of 2 parts freshly prepared spiroindane, 2 parts of dithiooxamide, 4 parts of Siloid 244 finely powdered silicon dioxide, 7.4 parts Pliolite VT polyvinyl toluene resin, and 86 parts of commercial grade heptane. The sheet is again dried under conditions of subdued light at room temperature to produce a heat-sensitive copy-sheet material which is desensitizable by actinic radiation.
The coated copy-sheet material is placed with its coated surface in contact with a graphic original of which a copy is desired, in this case an original typewritten on opaque paper, and the composite is subjected briefly to intense radiation rich in infra-red, applied through the sheet in accordance with therrnographic front-printing procedures. A right-reading copy as viewed through the transparent backing, having infra-red-absorptive blueblack image areas on a translucent background, is obtained.
A portion of the imaged surface of the copy is next irradiated for three minutes with ultraviolet light from a BH-6 high pressure mercury arc lamp held six inches away. The remaining area is protected from the ultraviolet radiation with a suitable shield. The protected background areas remain visibly heat-sensitive when briefiy subjected to a C. test bar; the irradiated background areas are found to be stabilized against visible change on brief contact with a test bar heated to C.
The copy thus formed has further utility in the preparation of additional reproductions on prepared receptor paper. The imaged coated surface of the sheet is placed in contact with the coated surface of a receptor sheet consisting of SO-lb. basis white opaque bond paper having a coating of the dried residue of a l-mil layer of a ballrnilled mixture of 3 parts of nickel stearate, 2 parts of Siloid 244 silicon dioxide, 4 parts of Lemac 1000 polyvinyl acetate resin, and 46 parts of methyl ethyl ketone. The composite is subjected to brief exposure to intense irradiation applied through the transparent film surface of the imaged copy-sheet and in accordance with the thermographic copying process, producing a further copy, in the form of black image areas against a clean white background, on the receptor sheet. In this first reproduction of the initial copy, the letter images obtained from the ultraviolet treated and the non-treated areas of the copy-sheet are of identical high quality.
Additional reproductions are made on further receptor sheets by repetition of the process described. After the first few copies, the letter images in the areas corresponding to the areas of the copy-sheet shielded from ultraviolet irradiation are found to be noticeably thickened and the background areas partially darkened, the deterioration of quality becoming increasingly apparent in further copies; whereas in the areas corresponding to the ultraviolet-treated areas of the copy-sheet, the images remain clear and sharp and the background areas remain unchanged through as many as twenty or more of such reproductions.
Many normally non-liquid polymeric organic filmforming materials which are further polymerized or crosslinked on exposure to actinic radiation have previously been described, and such polymers which are in addition normally thermoplastic, stable under prolonged storage in the absence of such radiation, non-volatile and nondecomposing under copy-sheet storage and use conditions, and preferably colorless or only slightly colored, are all found to be useful photosensitive materials in the practice of the invention. These include: soluble solid thermoplastic photocrosslinkable polycondensation products of glycols, such as decamethylene glycol, with unsaturated dicarhoxylic acids such as cinnamylidenemalonic acid, crotonylidenemalonic acid, o-nitrocinnamylidenemalonic acid, naphthyl allylidenemalonic acid, and
N-methylquinolidene-Z-ethylidenemalonic acid; the soluble solid thermoplastic photocrosslinkable reaction product of vinyl acetate and vinylazidophthalate with or without small proportions of vinyl alcohol residues; the soluble solid thermoplastic photocrosslinkable polymeric reaction products of acetophenone with styrene-maleic anhydridel-(betahydroxy ethoxyjbenzaldehyde or with methacrylic acid-4-(gammahydroxy propoxy)benzaldehyde intermediate products; the soluble solid thermoplastic photocrosslinkable polymeric reaction products of 4- hydroxyethoxy cinnamic acid with styrene-maleic anhydride copolymer; and the soluble solid thermoplastic photocrosslinkable polymeric reaction products of polyaminostyrene and cinnamoyl chloride.
Examples of illustrative classes and species of chemically inter-reactive image-forming materials have been provided. Many other classes of reactants suitable for heat-sensitive copy-sheet formulation have been described and are equally useful. The several components must of course be selected and applied so as to prevent or minimize pro-reaction. For example, the use of solvents or solvent systems which permit mutual solution and prereaction of chemical inter-reactants during coating is to be avoided. Also to be avoided are such components as tend to greatly alter or completely inhibit the desired radiation-induced polymerization or cross-linking reaction, such for example as materials having negative catalytic or inhibitor characteristics for a particular polymer or excessive amounts of opaque pigments.
Much the same considerations apply with respect to the physically convertible copy-sheets. The photosensitive material must be capable of retaining its initial physical form under normal storage and use conditions, must be susceptible of visible alteration, by appropriate modification of physical form, when briefly heated to a temperature within the range available in the thermoplastic copying process, and must be readily polymerized or cross-linked and rendered heat-resistant on exposure to actinic radiation. Where fusible components such as particulate waxes or other light-diffusing materials are to be included, it'is ordinarily desirable to select particulate and polymeric materials having as nearly as possible the same refractive index and which in addition form non-crystallizing compatible blends.
Many, if not all, of the presently available photosensitive polymeric binder materials useful in the practiceof the invention are highly sensitive to actinic radiation in the ultraviolet range, being somewhat less readily susceptible to visible light. The incorporation of appropriate activating dyes or the like is known to shift the sensitivity range of such materials and such modification is contemplated as coming within the ambit of the invention. Other variations and modifications will be apparent from the foregoing description.
What is claimed is as follows:
1. A heat-sensitive copy-sheet product capable of undergoing permanent visible change on momentary contact with a heated metal test bar at a conversion temperature within the approximate range of 60 to 150 C. and of being stabilized against a said change on said contact by moderate exposure to actinic radiation, said product consisting of a composite of a source sheet and a receptor sheet component in face-to-face contact, said receptor sheet component including a surface layer comprising a normally solid organic acid salt of a noble metal, said source sheet component including a surface layer comprising an organic reducing agent for the noble metal ions, and at least one of said layers including a soluble solid thermoplastic photocrosslinkable organic film-forming polymer material which undergoes an increase in softening temperature of at least about 10 C. under exposure to actinic radiation from a BH6 high pressure mercury arc lamp at 6 inches for 2 minutes, the softening temperature being determined with the sample between cover-glasses under a weight of grams and under a uniform rate of temperature increase of 1-3 C. per minute.
2. The copy-sheet product of claim 1 in which said receptor sheet component includes a surface layer comprising a normally solid organic acid salt of silver and a protective coating of the soluble solid thermoplastic photocrosslinkable organic film-forming polymer material.
3. A receptor sheet suitable for use as a component of the heatsensitive copy-sheet product of claim 1 and comprising a thin flexible sheet backing having a surface layer comprising a normally solid organic acid salt of silver and a protective coating of the soluble solid thermoplastic photocrosslinkable organic film-forming polymer material.
A heat-sensitive copy-sheet consisting essentially of a strongly colored thin flexible paper backing and an optically discontinuous and non-transparent heat-transparentizable blushed coating of a soluble solid thermoplastic transparent photocrosslinkable organic film-forming polymer materials which undergoes an increase of at least about 10 C. irr softening temperature on exposure to actinic radiation from a BH6 high pressure mercury arc lamp at 6 inches for 2 minutes, the softening temperature being determined with the sample between cover glasses under a weight of 5 grams and under a uniform rate of temperature increase of l3 C. per minute.
5. A heat-sensitive copy-sheet consisting essentially of a transparent thin flexible backing and an optically discontinuous and non-transparent heat-transparentizable blushed coating of a soluble solid thermoplastic transparent photocrosslinkable organic film-forming polymer material which undergoes an increase of at least about 10 C. in softening temperature on exposure to actinic radiation from a Bil-6 hi h pressure mercury arc lamp at 6 inches for 2 minutes,,the softening temperature being determined with the sample between cover glasses under a weight of 5 grams and under a uniform rate of temperature increase of l3 C. per minute.
6. A heat-sensitive copy-sheet consisting essentially of a thin flexible paper-like backing and a visibly heatsensitive chemically reactive coating capable on brief heating to a conversion temperature within the approximate range of to C. of converting to a permanently visibly distinct appearance by chemical reaction and capable of being rendered resistant to such action by moderate exposure to actinic radiation, said coating being further characterized as including a soluble solid thermoplastic photocrosslinkable organic film-forming polymeric binder material which undergoes an increase of at least about 10 C. in softening temperature on exposure to actinic radiation from a BH6 high pressure mercury arc lamp at 6 inches for 2 minutes, the softening temperature being determined with the sample between cover glasses under a weight of 5 grams andunder a uniform rate of temperature increase of 13 C. per minute.
7. A heat-sensitive copy-sheet consisting essentially of a thin flexible pa er-like backing and a visibly heatsensitive chemically reactive coating capable on brief heating to a conversion temperature within the approximate range of 60 to 150 C. of converting to a permanently visibly distinct appearance by chemical reaction and capable of being rendered resistant to such action by moderate exposure to actinic radiation, said coating comprising a uniform mixture of components consisting essentially of chemical co-reactants capable of undergoing visible co-reaction at said conversion temperature maintained in heat-reactive relationship by a soluble solid thermoplastic transparent photocrosslinkable organic filmforming polymeric binder material which undergoes an increase of at least about 10 C. in softening temperature on exposure to actinic radiation from a Eli-6 high pressure mercury arc lamp at 6 inches for 2 minutes, the softening temperature being determined with the sample between cover glasses under a weight of 5 grams and under a uniform rate of temperature increase of 13 C. per minute.
8. A heat-sensitive copy-sheet consisting essentially of a thin flexible paper-like backing and a visibly heatsensitive chemically reactive coating capable on brief heating to a conversion temperature within the approximate range of 60 to 150 C. of converting to a permanently visibly distinct appearance by chemical reaction and capable of being rendered resistant to such action by moderate exposure to actinic radiation, said coating comprising in order a layer of a first chemical reactant material, a thin separating layer of a soluble solid thermoplastic photosensitive organic film-forming polymeric binder material which undergoes an increase in softening temperature of at least about C. on exposure to actinic radiation from a BH6 high pressure mercury arc lamp at 6 inches for 2 minutes, and a layer of a second chemical reactant material, said first and second chemical reactant materials being capable of undergoing Visible co-reaction at said conversion temperature, the softening temperature of the binder material being determined with the sample between cover glasses under a weight of 5 grams and under a uniform rate of temperature increase of 1-3" C. per minute.
9. A heat-sensitive copy-sheet consisting essentially of a thin flexible paper-like backing and a visibly heatsensitive chemically reactive coating capable on brief heating to a conversion temperature within the approximate range of 60 to 150 Ci of converting to a permanently visibly distinct appearance by chemical reaction and capable of being rendered resistant to such action by moderate exposure to actinic radiation, said coating comprising a normally solid organic acid salt of a noble metal ion, an organic reducing agent for said metal ion, and a soluble solid thermoplastic photosensitive organic film-forming polymeric binder material which undergoes an increase in softening temperature :of at least about 10 C. on exposure to actinic radiation from a BH-6 high pressure mercury arc lamp at 6 inches for 2 minutes, the softening temperature being determined with the sample between cover glasses under a weight of 5 grams and under a uniform rate of temperature increase of 13 C. per minute.
References Cited by the Examiner UNITED STATES PATENTS 2,859,351 11/1958 Clark et al. 11736.7 2,880,110 3/1959 Miller l1736.7 2,919,349 12/ 1959 Kuhrmeyer 250- 2,927,039 3/1960 Vander Weel 250-65 3,057,999 10/1962 Newman et al. 11736.7 3,060,024 10/1962 Berg et a1 1173 6.1 3,094,417 6/1963 Workman 11736.2 XR 3,094,619 6/1963 Grant 11736.8 XR 3,097,096 7/1963 Oster 250-65.1 3,100,702 8/1963 Rauner et al 11736.1 3,107,174 10/1963 Wartman 11736.2
WILLIAM D. MARTIN, Primary Examiner.
MURRAY KATZ, Examiner.

Claims (1)

1. A HEAT-SENSITIVE COPY-SHEET PRODUCT CAPABLE OF UNDERGOING PERMANENT VISIBLE CHANGE ON MOMENTARY CONTACT WITH A HEATED METAL TEST BAR AT A CONVERSION TEMPERATURE WITHIN THE APPROXIMATE RANGE OF 60 TO 150*C. AND OF BEING STABILIZED AGAINST A SAID CHANGE ON SAID CONTACT BY MODERATE EXPOSURE TO ACTINIC RADIATION, SAID PRODUCT CONSISTING OF A COMPOSITE OF A SOURCE SHEET AND A RECEPTOR SHEET COMPONENT IN FACE-TO-FACE CONTACT, SAID RECEPTOR SHEET COMPONENT INCLUDING A SURFACE LAYER COMPRISING A NORMALLY SOLID ORGANIC ACID SALT OF A NOBLE METAL, SAID SOURCE SHEET COMPONENT INCLUDING A SURFACE LAYER COMPRISING AN ORGANIC REDUCING AGENT FOR THE NOBLE METAL IONS, AND AT LEAST ONE OF SAID LAYERS INCLUDING A SOLUBLE SOLID THERMOPLASTIC PHOTOCROSSLINKABLE ORGANIC FILM-FORMING POLYMER MATERIAL WHICH UNDERGOES AN INCREASE IN SOFTENING TEMPERATURE OF AT LEAST ABOUT 10*C. UNDER EXPOSURE TO ACTINIC RADIATION FROM A BH-6 HIGH PRESSURE MERCURY ARC LAMP AT 6 INCHES FOR 2 MINUTES, THE SOFTENING TEMPERATURE BEING DETERMINED WITH THE SAMPLE BETWEEN COVER-GLASSES UNDER A WEIGHT OF 5 GRAMS AND UNDER A UNIFORM RATE OF TEMPERATURE INCREASE OF 1-3*C. PER MINUTE.
US230735A 1962-10-15 1962-10-15 Heat and photosensitive copy sheet Expired - Lifetime US3218168A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US230735A US3218168A (en) 1962-10-15 1962-10-15 Heat and photosensitive copy sheet
US490621A US3282692A (en) 1962-10-15 1965-09-27 Photocrosslinkable material and method of copying

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US230735A US3218168A (en) 1962-10-15 1962-10-15 Heat and photosensitive copy sheet
US490621A US3282692A (en) 1962-10-15 1965-09-27 Photocrosslinkable material and method of copying

Publications (1)

Publication Number Publication Date
US3218168A true US3218168A (en) 1965-11-16

Family

ID=26924504

Family Applications (2)

Application Number Title Priority Date Filing Date
US230735A Expired - Lifetime US3218168A (en) 1962-10-15 1962-10-15 Heat and photosensitive copy sheet
US490621A Expired - Lifetime US3282692A (en) 1962-10-15 1965-09-27 Photocrosslinkable material and method of copying

Family Applications After (1)

Application Number Title Priority Date Filing Date
US490621A Expired - Lifetime US3282692A (en) 1962-10-15 1965-09-27 Photocrosslinkable material and method of copying

Country Status (1)

Country Link
US (2) US3218168A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3350205A (en) * 1964-04-27 1967-10-31 Xerox Corp Method of image reproduction by photopolymerization and blushing
US3377165A (en) * 1964-01-22 1968-04-09 Minnesota Mining & Mfg Process of copying utilizing a blush lacquer coating and a photodecomposable progenitor of a plasticizer
US3460946A (en) * 1966-02-03 1969-08-12 Minnesota Mining & Mfg Image receptor sheets containing organic silver salts and metal ion image
US3481738A (en) * 1966-09-21 1969-12-02 Ball Brothers Co Inc Presensitized photoengraving plate and method of making same
US3514305A (en) * 1965-10-20 1970-05-26 Us Plywood Champ Papers Inc Reproduction of images from printed surfaces
US3529963A (en) * 1966-08-23 1970-09-22 Du Pont Image-yielding elements and processes
DE1671571B1 (en) * 1966-09-15 1971-07-08 Phonocopy Inc ELECTROTHERMOGRAPHIC RECORDING METHOD AND THE LAYER CARRIER USED IN IT
US3617289A (en) * 1966-12-10 1971-11-02 Fuji Photo Film Co Ltd Stabilization process for thermally developable light-sensitive elements
US3630732A (en) * 1966-06-24 1971-12-28 Agfa Gevaert Nv Thermographic recording material
US3645739A (en) * 1966-02-21 1972-02-29 Fuji Photo Film Co Ltd Thermally developable light-sensitive elements
EP0230992A2 (en) * 1986-01-29 1987-08-05 Lexmark International, Inc. Transfer element and process for printing radiation defined images using said element

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2859351A (en) * 1951-02-02 1958-11-04 Minnesota Mining & Mfg Method of making permanent facsimile copies
US2880110A (en) * 1954-12-02 1959-03-31 Minnesota Mining & Mfg Heat-sensitive copying-paper
US2919349A (en) * 1956-04-02 1959-12-29 Minnesota Mining & Mfg Shadow thermoprinting
US2927039A (en) * 1957-03-07 1960-03-01 Labelon Tape Co Inc Heat sensitive copying sheet
US3057999A (en) * 1960-03-31 1962-10-09 Columbia Ribbon & Carbon Thermographic copy paper and process
US3060024A (en) * 1959-09-11 1962-10-23 Du Pont Photopolymerization process for reproducing images
US3094619A (en) * 1961-01-03 1963-06-18 Minnesota Mining & Mfg Ultra-violet radiation-desensitizable thermographic copy-sheet and method
US3094417A (en) * 1961-01-03 1963-06-18 Minnesota Mining & Mfg Heat sensitive copy sheet, process of making and using
US3097096A (en) * 1955-01-19 1963-07-09 Oster Gerald Photopolymerization with the formation of relief images
US3100702A (en) * 1960-03-30 1963-08-13 Eastman Kodak Co Dry processed photothermographic printing plate and process
US3107174A (en) * 1958-10-20 1963-10-15 Minnesota Mining & Mfg Heat sensitive copy sheet and method of making

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2859351A (en) * 1951-02-02 1958-11-04 Minnesota Mining & Mfg Method of making permanent facsimile copies
US2880110A (en) * 1954-12-02 1959-03-31 Minnesota Mining & Mfg Heat-sensitive copying-paper
US3097096A (en) * 1955-01-19 1963-07-09 Oster Gerald Photopolymerization with the formation of relief images
US2919349A (en) * 1956-04-02 1959-12-29 Minnesota Mining & Mfg Shadow thermoprinting
US2927039A (en) * 1957-03-07 1960-03-01 Labelon Tape Co Inc Heat sensitive copying sheet
US3107174A (en) * 1958-10-20 1963-10-15 Minnesota Mining & Mfg Heat sensitive copy sheet and method of making
US3060024A (en) * 1959-09-11 1962-10-23 Du Pont Photopolymerization process for reproducing images
US3100702A (en) * 1960-03-30 1963-08-13 Eastman Kodak Co Dry processed photothermographic printing plate and process
US3057999A (en) * 1960-03-31 1962-10-09 Columbia Ribbon & Carbon Thermographic copy paper and process
US3094619A (en) * 1961-01-03 1963-06-18 Minnesota Mining & Mfg Ultra-violet radiation-desensitizable thermographic copy-sheet and method
US3094417A (en) * 1961-01-03 1963-06-18 Minnesota Mining & Mfg Heat sensitive copy sheet, process of making and using

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3377165A (en) * 1964-01-22 1968-04-09 Minnesota Mining & Mfg Process of copying utilizing a blush lacquer coating and a photodecomposable progenitor of a plasticizer
US3350205A (en) * 1964-04-27 1967-10-31 Xerox Corp Method of image reproduction by photopolymerization and blushing
US3514305A (en) * 1965-10-20 1970-05-26 Us Plywood Champ Papers Inc Reproduction of images from printed surfaces
US3460946A (en) * 1966-02-03 1969-08-12 Minnesota Mining & Mfg Image receptor sheets containing organic silver salts and metal ion image
US3645739A (en) * 1966-02-21 1972-02-29 Fuji Photo Film Co Ltd Thermally developable light-sensitive elements
US3630732A (en) * 1966-06-24 1971-12-28 Agfa Gevaert Nv Thermographic recording material
US3529963A (en) * 1966-08-23 1970-09-22 Du Pont Image-yielding elements and processes
DE1671571B1 (en) * 1966-09-15 1971-07-08 Phonocopy Inc ELECTROTHERMOGRAPHIC RECORDING METHOD AND THE LAYER CARRIER USED IN IT
US3481738A (en) * 1966-09-21 1969-12-02 Ball Brothers Co Inc Presensitized photoengraving plate and method of making same
US3617289A (en) * 1966-12-10 1971-11-02 Fuji Photo Film Co Ltd Stabilization process for thermally developable light-sensitive elements
EP0230992A2 (en) * 1986-01-29 1987-08-05 Lexmark International, Inc. Transfer element and process for printing radiation defined images using said element
EP0230992A3 (en) * 1986-01-29 1989-03-29 International Business Machines Corporation Transfer element and method for radiation defined images

Also Published As

Publication number Publication date
US3282692A (en) 1966-11-01

Similar Documents

Publication Publication Date Title
US3094619A (en) Ultra-violet radiation-desensitizable thermographic copy-sheet and method
US3793025A (en) Thermorecording
US3514597A (en) Thermographic recording processes and materials
US3619157A (en) Thermo recording
US3218166A (en) Heat sensitive copy sheet
US3094417A (en) Heat sensitive copy sheet, process of making and using
US3628953A (en) Thermorecording
US3280735A (en) Heat-copying process
US4588674A (en) Laser imaging materials comprising carbon black in overlayer
US3260612A (en) Thermographic recording process and heat-sensitive elements therefor
US3218168A (en) Heat and photosensitive copy sheet
US3107174A (en) Heat sensitive copy sheet and method of making
US3859094A (en) Sheet material useful in image transfer techniques
US2967784A (en) Thermographic copying paper
US3685993A (en) Lithographic plate with resin binder containing silver soap oxidizing agent
US3898086A (en) Sheet material useful in image transfer techniques
US3941596A (en) Thermographic processes using polymer layer capable of existing in metastable state
US3418468A (en) Process for the production of projection transparencies
US4389473A (en) Production of transfer material
US3679410A (en) Heat-sensitive recording material
US3795532A (en) Wide latitude copy sheet
US2916395A (en) Heat-sensitive copy-paper
US3833441A (en) Thermographic processes
US3664858A (en) Heat-sensitive copy-sheet
US3360367A (en) Copying of graphic images