EP0836116B1 - A sensitivity-increasing recording process for a photosensitive thermally developable photographic material - Google Patents

A sensitivity-increasing recording process for a photosensitive thermally developable photographic material Download PDF

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Publication number
EP0836116B1
EP0836116B1 EP97202521A EP97202521A EP0836116B1 EP 0836116 B1 EP0836116 B1 EP 0836116B1 EP 97202521 A EP97202521 A EP 97202521A EP 97202521 A EP97202521 A EP 97202521A EP 0836116 B1 EP0836116 B1 EP 0836116B1
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EP
European Patent Office
Prior art keywords
thermally developable
photographic material
developable photographic
photosensitive
photosensitive thermally
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
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EP97202521A
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German (de)
French (fr)
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EP0836116A1 (en
Inventor
Luc Leenders
Jacobus Bosschaerts
Robert Overmeer
Eddie Daems
Leo Oelbrandt
Hans Strijckers
Thomas Zehetmaier
Jürgen Müller
Friedrich Stumpf
Gerald Halbedl
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Agfa Gevaert NV
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Agfa Gevaert NV
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Publication date
Priority claimed from DE19636235A external-priority patent/DE19636235A1/en
Priority claimed from US08/812,450 external-priority patent/US5804355A/en
Application filed by Agfa Gevaert NV filed Critical Agfa Gevaert NV
Publication of EP0836116A1 publication Critical patent/EP0836116A1/en
Application granted granted Critical
Publication of EP0836116B1 publication Critical patent/EP0836116B1/en
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Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/494—Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
    • G03C1/498—Photothermographic systems, e.g. dry silver
    • G03C1/49881—Photothermographic systems, e.g. dry silver characterised by the process or the apparatus
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03D—APPARATUS FOR PROCESSING EXPOSED PHOTOGRAPHIC MATERIALS; ACCESSORIES THEREFOR
    • G03D13/00—Processing apparatus or accessories therefor, not covered by groups G11B3/00 - G11B11/00
    • G03D13/002—Heat development apparatus, e.g. Kalvar
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/08—Sensitivity-increasing substances
    • G03C1/10—Organic substances
    • G03C1/12—Methine and polymethine dyes
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/08—Sensitivity-increasing substances
    • G03C1/10—Organic substances
    • G03C1/12—Methine and polymethine dyes
    • G03C1/14—Methine and polymethine dyes with an odd number of CH groups
    • G03C1/20—Methine and polymethine dyes with an odd number of CH groups with more than three CH groups
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/494—Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
    • G03C1/498—Photothermographic systems, e.g. dry silver
    • G03C1/49836—Additives
    • G03C1/49845—Active additives, e.g. toners, stabilisers, sensitisers
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/494—Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
    • G03C1/498—Photothermographic systems, e.g. dry silver
    • G03C1/4989—Photothermographic 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

Definitions

  • the present invention relates to a sensitivity-increasing recording process for photographic materials in which information-wise exposure is carried out during heating.
  • Thermal imaging or thermography is a recording process wherein images are generated by the use of imagewise modulated thermal energy.
  • thermography three approaches are known:
  • Thermographic materials of type 3 become photothermographic if a photosensitive agent is present which after exposure to UV, visible or IR light is capable of catalyzing or participating in a thermographic process bringing about changes in colour or optical density.
  • photothermographic materials are the so called “Dry Silver”photothermographic materials of the 3M Company, which are reviewed by D.A. Morgan in “Handbook of Imaging Science”, edited by A.R. Diamond, page 43, published by Marcel Dekker in 1991.
  • DOS 2 248 545 discloses a copying process characterized in that the whole surface of a thermally developable photosensitive silver material is subjected before the complete execution of the exposure to a uniform auxiliary thermal treatment at a temperature, that is within the suitable development temperature range for the photosensitive material, and to thermal development after exposure; and that, in a subclaim, the photosensitive material can also be subjected to auxiliary heating during the exposure thereof.
  • the specification and invention examples give no indication of the efficacity of auxiliary heating during exposure.
  • JP-A-61 196243 discloses a scan type exposure and development installation having as distinctive feature that it has a rotation drum which has a thermal development photosensitive material wound around it and uses the axis center as rotation axis, an exposure head which is positioned opposite the circumference face of the rotation drum and moves in the axis direction of the rotation drum in response to the rotation of the rotation drum, and a heating head which is positioned opposite the circumference face of the rotation drum and moves in the axis direction of the rotation drum in response to the rotation of the rotation drum.
  • the thermal heating head can be a laser heating head and heating development may be carried out while scanning the thermal development photosensitive material and as a result development and exposure may be carried out with the same installation at almost the same time thereby shortening the total treatment time of exposure and development.
  • a recording process comprising the steps of: information-wise exposing to radiation a photosensitive thermally developable photographic material, thereby producing a latent image; and heating the photosensitive thermally developable photographic material, characterized in that the photosensitive thermally developable photographic material is on one and the same holding or guiding means during both the information-wise exposure step and the heating step; the information-wise exposure step is carried out pixelwise during the heating step; the exposure step begins after the start of the heating step; and the duration of the exposure step is less than one tenth of the duration of the heating step.
  • a method of increasing the photosensitivity of a photosensitive thermally developable photographic material characterized in that the photosensitive thermally developable photographic material is on one and the same holding or guiding means during both the information-wise exposure step and the heating step; the information-wise exposure step is carried out pixelwise during said heating step; the exposure step begins after the start of the heating step; and the duration of said exposure step is less than one tenth of the duration of the heating step.
  • the inventors of the present invention surprisingly have found that the preheating of materials resulted in thermally developable photographic materials requiring shorter exposure times than with prior art processes in which unheated materials are exposed to recording radiation. This showed that materials upon heating are more sensitive to recording radiation and enables the apparatus to be simplified.
  • the duration of the exposure step be less than one hundredth of the duration of the heating step.
  • thermal development of the photosensitive thermally developable photographic material is carried out during the heating step, during which a visible image is produced from the latent image resulting from the exposure step.
  • the heating step begins before the start of the exposure step and ends after thermal development to produce a visible image is complete.
  • Photographic materials and photosensitive thermally developable photographic materials may, according to the present invention, be exposed with radiation of wavelength between an X-ray wavelength and a 5 microns wavelength with the image being obtained by pixel-wise exposure with a finely focused light source, such as a CRT light source; a UV, visible or IR wavelength laser, such as a He/Ne-laser or an IR-laser diode, e.g. emitting at 780nm, 830nm or 850nm; or a light emitting diode, for example one emitting at 659nm. Exposure with infra-red light or visible light is preferred, visible light in the wavelength range 600nm to 700nm being particularly preferred. Exposure with an infra-red emitting laser diode is preferred, according to the present invention.
  • a finely focused light source such as a CRT light source
  • a UV, visible or IR wavelength laser such as a He/Ne-laser or an IR-la
  • the photosensitive thermally developable photographic material may be heated during the exposure and the heating subsequent to the exposure by the same heating means. Furthermore, the photosensitive thermally developable photographic material may be heated prior to the exposure, during the exposure and during the heating subsequent to the exposure by the same heating means.
  • a heated drum is a preferred common heating means.
  • any sort of heat source can be used that enables the recording materials to be uniformly heated to the development temperature in a time acceptable for the application concerned e.g. contact heating with for example a heated roller, a heated drum, a thermal head, radiative heating, microwave heating etc.
  • the preferred temperature of the photosensitive thermally developable photographic material during thermal development is between 110°C and 130°C.
  • At least two radiation beams move simultaneously over the photosensitive thermally developable photographic material the first of the radiation beams carrying out the information-wise exposing of the photosensitive thermally developable photographic material and the second of which heats the information-wise exposed photosensitive thermally developable photographic material to a uniform development temperature.
  • the photosensitive thermally developable photographic material preferably contains an infrared sensitizer or a visible light sensitizer and particularly preferably further contains photosensitive silver halide, an organic reducing agent and a binder.
  • the use in the present invention of a photosensitive thermally developable photographic material including a gelatinous silver halide emulsion layer is preferred.
  • the use in the present invention of a photosensitive thermally developable photographic material further containing a substantially light-insensitive organic silver salt with which the photosensitive silver halide in catalytic association and an organic reducing agent for the substantially light-insensitive organic silver salt in thermal working relationship therewith is particularly preferred.
  • the photosensitive thermally developable photographic material may have a layer system in which the ingredients are dispersed in different layers, with the proviso that the image-forming process can take place.
  • the photosensitive silver halide or substantially light-insensitive organic silver salt in the case of photosensitive thermally developable photographic materials containing photosensitive silver halide and an organic reducing agent optionally further containing a substantially light-insensitive organic silver salt, the photosensitive silver halide or substantially light-insensitive organic silver salt, if present, must be in thermal working relationship with the organic reducing agent i.e. during the thermal development process the reducing agent must be present in such a way that it is able to diffuse to the photosensitive silver halide or the substantially light-insensitive organic silver salt particles so that reduction of the silver halide or organic silver salt can take place; and the photosensitive silver halide is in catalytic association with the substantially light-insensitive organic silver salt, if present.
  • the photosensitive silver halide used in the present invention may be employed in a range of 0.1 to 100 mol percent; preferably, from 0.2 to 80 mol percent; particularly preferably from 0.3 to 50 mol percent; especially preferably from 0.5 to 35 mol %; and especially from 1 to 12 mol % of substantially light-insensitive organic silver salt.
  • the silver halide may be any photosensitive silver halide such as silver bromide, silver iodide, silver chloride, silver bromoiodide, silver chlorobromoiodide, silver chlorobromide etc.
  • the silver halide may be in any form which is photosensitive including, but not limited to, cubic, orthorhombic, tabular, tetrahedral, octagonal etc. and may have epitaxial growth of crystals thereon.
  • the silver halide used in the present invention may be employed without modification. However, it may be chemically sensitized with a chemical sensitizing agent such as a compound containing sulphur, selenium, tellurium etc., or a compound containing gold, platinum, palladium, iron, ruthenium, rhodium or iridium etc., a reducing agent such as a tin halide etc., or a combination thereof.
  • a chemical sensitizing agent such as a compound containing sulphur, selenium, tellurium etc., or a compound containing gold, platinum, palladium, iron, ruthenium, rhodium or iridium etc.
  • a reducing agent such as a tin halide etc.
  • the photosensitive thermally developable photographic material may contain an infra-red sensitizer or a visible light sensitizer.
  • Suitable sensitizers include cyanine, merocyanine, styryl, hemicyanine, oxonol, hemioxonol and xanthene dyes.
  • Useful cyanine dyes include those having a basic nucleus, for example a thiazoline nucleus, an oxazoline nucleus, a pyrroline nucleus, a pyridine nucleus, an oxazole nucleus, a thiazole nucleus, a selenazole nucleus and an imidazole nucleus.
  • Preferred merocyanine dyes include those having not only the above described basic nuclei but also acid nuclei, for example a thiohydantoin nucleus, a rhodanine nucleus, an oxazolidinedione nucleus, a thiazolidinedione nucleus, a barbituric acid nucleus, a thiazolinone nucleus, a malononitrile nucleus and a pyrazolone nucleus.
  • those having imino groups or carboxyl groups are particularly preferred.
  • Suitable infra-red sensitizers include those disclosed in EP-A's 465 078, 559 101, 616 014 and 635 756, JN's 03-080251, 03-163440, 05-019432, 05-072662 and 06-003763 and US-P's 4,515,888, 4,639,414, 4,713,316, 5,258,282 and 5,441,866.
  • IR-sensitizing dyes according to general formula (I) suitable for use according to the present invention are:
  • the photosensitive thermally developable photographic material further includes a supersensitizer.
  • Preferred supersensitzers are selected from the group of compounds consisting of: mercapto-compounds, disulfide-compounds, stilbene compounds, organoborate compounds and styryl compounds.
  • Suitable supersensitizers for use with infra-red spectral sensitizers are disclosed in EP-A 559 228, EP-A 587 338, US-P 3,877,943, US-P 4,873,184 and unpublished European Patent Application EP 96202107.7.
  • Preferred substantially light-insensitive organic silver salts used in the photosensitive thermally developable photographic material used in the present invention are silver salts of aliphatic carboxylic acids known as fatty acids, wherein the aliphatic carbon chain has preferably at least 12 C-atoms, e.g. silver laurate, silver palmitate, silver stearate, silver hydroxystearate, silver oleate and silver behenate, which silver salts are also called "silver soaps"; silver dodecyl sulphonate described in US-P 4,504,575; and silver di-(2-ethylhexyl)-sulfosuccinate described in EP-A 227 141.
  • Modified aliphatic carboxylic acids with thioether group as described e.g. in GB-P 1,111,492 and other organic silver salts as described in GB-P 1,439,478, e.g. silver benzoate and silver phthalazinone, may be used likewise to produce a thermosensitive silver image.
  • Silver imidazolates and the substantially light-insensitive inorganic or organic silver salt complexes described in US-P 4,260,677 are also suitable.
  • substantially light-insensitive organic silver salt for the purposes of the present invention also includes mixtures of organic silver salts.
  • the silver halide may be added to the photosensitive thermally developable photographic material in any fashion which places it in catalytic proximity to the substantially light-insensitive organic silver salt.
  • Photosensitive silver halide and substantially light-insensitive organic silver salt which are separately formed, i.e. ex-situ or "preformed", in a binder can be mixed prior to use to prepare a coating solution, but they may be blended for a long period of time prior to use.
  • a particularly preferred mode of preparing the emulsion of organic silver salt and photosensitive silver halide for coating of the photosensitive thermally developable photographic material from solvent media, according to the present invention is that disclosed in US-P 3,839,049, but other methods such as those described in Research Disclosure, June 1978, item 17029 and US-P 3,700,458 may also be used.
  • Suitable organic reducing agents for use in the photosensitive thermally developable photographic material used in the present invention are organic compounds containing at least one active hydrogen atom linked to 0, N or C, such as is the case with, mono-, bis-, tris- or tetrakis-phenols; mono- or bis-naphthols; di- or polyhydroxy-naphthalenes; di- or polyhydroxybenzenes; hydroxymonoethers such as alkoxynaphthols, e.g. 4-methoxy-1-naphthol described in US-P 3,094,41; pyrazolidin-3-one type reducing agents, e.g.
  • PHENIDONETM pyrazolin-5-ones; indan-1,3-dione derivatives; hydroxytetrone acids; hydroxytetronimides; 3-pyrazolines; pyrazolones; reducing saccharides; aminophenols e.g. METOLTM; p-phenylenediamines, hydroxylamine derivatives such as for example described in US-P 4,082,901; reductones e.g. ascorbic acids; hydroxamic acids; hydrazine derivatives; amidoximes; n-hydroxyureas; and the like, see also US-P 3,074,809, 3,080,254, 3,094,417 and 3,887,378.
  • Particularly preferred catechol-type reducing agents are described in EP-A 692 733 and EP-A 599 369.
  • Polyphenols such as the bisphenols used in the 3M Dry SilverTM materials, sulfonamide phenols such as used in the Kodak DacomaticTM materials, and naphthols are particularly preferred for photosensitive thermally developable photographic materials on the basis of silver halide/organic silver salt/reducing agent.
  • reducing agents being considered as primary or main reducing agents may be used in conjunction with so-called auxiliary reducing agents.
  • auxiliary reducing agents that may be used in conjunction with the above-mentioned primary reducing agents are sulfonamidophenols as described in the periodical Research Disclosure, February 1979, item 17842, in US-P 4,360,581 and 4,782,004, and in EP-A 423 891.
  • auxiliary reducing agents that may be used in conjunction with the above mentioned primary reducing agents are hydrazides such as disclosed in EP-A 762 196, sulfonyl hydrazide reducing agents such as disclosed in US-P 5,464,738; trityl hydrazides and formyl-phenyl-hydrazides such as disclosed in US-P 5,496,695; trityl hydrazides and formyl-phenyl-hydrazides with diverse auxiliary reducing agents such as disclosed in US-P 5,545,505, US-P 5.545.507 and US-P 5,558,983; acrylonitrile compounds as disclosed in US-P 5,545,515 and US-P 5,635,339; and organic reducing metal salts, e.g. stannous stearate described in US-P 3,460,946 and 3,547,648.
  • hydrazides such as disclosed in EP-A 762 196, sulfonyl hydrazi
  • the binder for the photosensitive thermally developable photographic material used in the present invention may be coatable from a solvent or aqueous dispersion and must themselves be film-forming or must be used in association with a film-forming binder.
  • Film-forming binders coatable from a solvent dispersion and usable in the present invention may be all kinds of natural, modified natural or synthetic resins or mixtures of such resins, wherein the organic silver salt can be dispersed homogeneously: e.g. polyurethanes, polyesters, polyamides, polycarbonates and polymers derived from ⁇ , ⁇ -ethylenically unsaturated compounds, polyvinyl acetals preferably polyvinylbutyral, and homopolymers and copolymers produced using monomers selected from the group consisting of: acrylonitrile, acrylamides, methacrylamides. methacrylates, acrylates, methacrylic acids, acrylic acids, vinyl esters, styrenes and alkenes; or mixtures thereof.
  • the organic silver salt can be dispersed homogeneously: e.g. polyurethanes, polyesters, polyamides, polycarbonates and polymers derived from ⁇ , ⁇ -ethylenically unsatur
  • the film-forming binder coatable from an aqueous dispersion used in the present invention may be all kinds of transparent or translucent water-dispersible or water soluble natural, modified natural or synthetic resins or mixtures of such resins, wherein the organic silver salt can be dispersed homogeneously for example proteins, such as gelatin and gelatin derivatives ; cellulose derivatives; polysaccharides; galactomannan; polyvinyl alcohol; polyvinylpyrrolidone; polyurethanes; polyesters; polyamides; polycarbonates; polymers derived from ⁇ , ⁇ -ethylenically unsaturated compounds, for example polyvinyl acetals, preferably polyvinylbutyral, and homopolymers and copolymers produced using monomers selected from the group consisting of: acrylonitrile, acrylamides, methacrylamides. methacrylates, acrylates, methacrylic acids, acrylic acids, vinyl esters, styrenes and alkenes; and latexe
  • binders or mixtures thereof may be used in conjunction with waxes or "heat solvents” also called “thermal solvents” or “thermosolvents” improving the reaction speed of the redox-reaction at elevated temperature.
  • the photosensitive thermally developable photographic material used according to the present invention may also contain at least one polycarboxylic acid and/or anhydride thereof in a molar percentage of at least 20 with respect to all the organic silver salt(s) present and in thermal working relationship therewith.
  • Preferred aromatic polycarboxylic acids are ortho-phthalic acid and 3-nitro-phthalic acid, tetrachlorophthalic acid, mellitic acid, pyromellitic acid and trimellitic acid and the anhydrides thereof.
  • the photosensitive thermally developable photographic material preferably contains in admixture with the organic silver salts and reducing agents a so-called toning agent known from thermography or photothermography.
  • Suitable toning agents are succinimide, phthalazine and the phthalimides and phthalazinones within the scope of the general formulae described in US-P 4,082,901 and the toning agents described in US-P 3,074,809, 3,446,648 and 3,844,797.
  • Particularly useful toning agents are the heterocyclic toner compounds of the benzoxazine dione or naphthoxazine dione type as described in GB-P 1,439,478, US-P 3,951,660 and US-P 5,599,647.
  • the photosensitive thermally developable photographic materials used in the present invention may also contain antihalation or acutance dyes which absorb light which has passed through the photosensitive thermally developable photographic material, thereby preventing its reflection. Such dyes may be incorporated into the photosensitive thermally developable photographic material or in any other layer of the photographic material of the present invention.
  • the photosensitive thermally developable photographic material used in the present invention may also contain additives such as free fatty acids, surface-active agents, silicone oil, e.g. BAYSILONETM ⁇ l A (from BAYER AG, GERMANY) ; ultraviolet light absorbing compounds; silica; colloidal silica; fine polymeric particles, e.g. of poly(methylmethacrylate); and/or optical brightening agents.
  • silicone oil e.g. BAYSILONETM ⁇ l A (from BAYER AG, GERMANY)
  • ultraviolet light absorbing compounds e.g. BAYSILONETM ⁇ l A (from BAYER AG, GERMANY)
  • silica colloidal silica
  • fine polymeric particles e.g. of poly(methylmethacrylate)
  • optical brightening agents e.g., optical brightening agents.
  • the support for the photosensitive thermally developable photographic material used in the present invention may be transparent, translucent or opaque, e.g. having a white light reflecting aspect and is preferably a thin flexible carrier made e.g. from paper, polyethene coated paper or transparent resin material, e.g. made of a cellulose ester, e.g. cellulose triacetate, corona and flame treated polypropylene, polystyrene, polymethacrylic acid ester, polycarbonate or polyester, e.g. polyethylene terephthalate or polyethylene naphthalate as disclosed in GB 1,293,676, GB 1,441,304 and GB 1,454,956.
  • a thin flexible carrier made e.g. from paper, polyethene coated paper or transparent resin material, e.g. made of a cellulose ester, e.g. cellulose triacetate, corona and flame treated polypropylene, polystyrene, polymethacrylic acid ester, polycarbonate or
  • the support may be in sheet, ribbon or web form and subbed if need be to improve the adherence to the thereon coated thermosensitive recording layer.
  • One or more backing layers may be provided to control physical properties such as curl or static.
  • the outermost layer of the side of the photosensitive thermally developable photographic material which is photosensitive may be a protective layer to avoid local deformation of the photosensitive thermally developable photographic material and to improve resistance against abrasion.
  • the protective layer preferably comprises a binder, which may be hydrophobic (solvent soluble) or hydrophilic (water soluble) e.g. as described in EP-A 614 769.
  • Hydrophilic binders are, however, preferred for the protective layer, as coating can be performed from an aqueous composition and mixing of the hydrophilic protective layer with the immediate underlayer can be avoided by using a hydrophobic binder in the immediate underlayer.
  • a protective layer used in the present invention may also contain at least one solid lubricant having a melting point below 150°C and at least one liquid lubricant at least one of these lubricants being a phosphoric acid derivative; and additional dissolved lubricating material and/or particulate material, e.g. talc particles, optionally protruding from the outermost layer.
  • the lubricant may be applied with or without a polymeric binder.
  • Such protective layers may also contain particulate material, e.g. talc particles, optionally protruding from the protective outermost layer as described in WO 94/11198.
  • particulate material e.g. talc particles
  • Other additives can also be incorporated therein e.g. colloidal particles such as colloidal silica.
  • the photosensitive thermally developable photographic materials used in the present invention may further include an antistatic layer.
  • Suitable antistatic layers are described in EP-A's 444 326, 534 006 and 644 456, US-P's 5,364,752 and 5,472,832 and DOS 4125758.
  • Particularly preferred antistatic layers are those based on polythiophene as disclosed in EP-A 628 560, US-P 5,354,613, US-P 5,372,924, US-P 5,370,981 and US-P 5,391,472.
  • any layer of the photosensitive thermally developable photographic materials used in the present invention may proceed by any thin-film coating technique known in the art.
  • any thin-film coating technique known in the art.
  • slide hopper coating is preferred, but other coating techniques such as dip coating and air knife coating may also be used. Details about such coating techniques can be found in "Modern Coating and Drying Technology" by Edward D. Cohen and Edgar B. Gutoff, published by VCH Publishers, Inc. 220 East 23rd Street, Suite 909 New York, NY 10010.
  • the photosensitive thermally developable photographic materials used in the present invention can be used for both the production of transparencies and reflection type prints.
  • the support will be transparent or opaque, e.g. having a white light reflecting aspect.
  • a paper base substrate is present which may contain white reflecting pigments, optionally also applied in an interlayer between the recording material and the paper base substrate. Should a transparent base be used, the base may be colourless or coloured, e.g. has a blue colour.
  • a polyethylene terephthalate (PET) foil pigmented with a blue pigment was first coated on both sides with a subbing layer consisting of a terpolymer latex of vinylidene chloride-methyl acrylate-itaconic acid (88/10/2) in admixture with colloidal silica (surface area 100m 2 /g). After stretching the foil in the transverse direction the foil had a thickness of 175 ⁇ m with coverages of the terpolymer and of the silica in the subbing layers of 170mg/m 2 and 40mg/m 2 respectively on each side of the PET-foil.
  • PET polyethylene terephthalate
  • the antihalation/antistatic layer was prepared by first adsorbing antihalation dye D01 onto the polymethyl methacrylate particles of LATEX01 by adding 55mg of D01 dissolved in ethyl acetate/g polymethyl methacrylate and then evaporating off the ethyl acetate.
  • a silver halide emulsion consisting of 3.11% by weight of silver halide particles consisting of 97mol% silver bromide and 3mol% silver iodide with a weight average particle size of 50nm, 0.47% by weight of GEL as dispersing agent in deionized water was prepared using conventional silver halide preparation techniques such as described, for example, in T.H. James, "The Theory of the Photographic Process", Fourth Edition, Macmillan Publishing Co. Inc., New York (1977), Chapter 3, pages 88-104.
  • the silver behenate/silver halide emulsion was prepared by adding a solution of 6.8kg of behenic acid in 67L of 2-propanol at 65°C to a 400L vessel heated to maintain the temperature of the contents at 65°C, converting 96% of the behenic acid to sodium behenate by adding with stirring 76.8L of 0.25M sodium hydroxide in deionized water, then adding with stirring 10.5kg of the above-described silver halide emulsion at 40°C and finally adding with stirring 48L of a 0.4M solution of silver nitrate in deionized water. Upon completion of the addition of silver nitrate the contents of the vessel were allowed to cool and the precipitate filtered off, washed, slurried with water, filtered again and finally dried at 40°C for 72 hours.
  • the emulsion layer coating composition for the photosensitive thermally developable photographic material was prepared by adding the following solutions or liquids to 40.86g of the above-mentioned silver behenate/silver halide emulsion in the following sequence with stirring: 10.87g of 2-butanone, 0.75g of a 9% solution of TMABP in methanol followed by 2 hours stirring, 1.3g of 2-butanone, 0.2g of a 11% solution of calcium bromide in methanol and 1.3g of 2-butanone followed by 30 minutes stirring, a solution consisting of 0.21g of LOWINOXTM 22IB46, 0.5g of TMPS and 9.24g of 2-butanone followed by 10 minutes stirring, 1.84g of a 0.11% methanol solution of SENSI followed by 30 minutes stirring and finally 4.35g of ButvarTM B76 were added followed by 45 minutes of stirring and then 4.79g of 2-butanone.
  • the PET-support subbed and coated with an antihalation/antistatic layer as described above was then doctor blade-coated at a blade setting of 150 ⁇ m on the side of the support not coated with a backside layer with the coating composition to a wet layer thickness of 80 ⁇ m followed by drying for 5 minutes at 80°C on an aluminium plate in a drying cupboard.
  • a protective layer coating composition for the photosensitive thermally developable photographic material was prepared by dissolving 4.08g of CAB and 0.16g of PMMA in 36.3g of 2-butanone and 4.16g of methanol adding the following solids or solution with stirring in the following sequence: 0.5g of phthalazine, 0.2g of 4-methylphthalic acid, 0.1g of tetrachlorophthalic acid, 0.2g of tetrachlorophthalic acid anhydride and a solution consisting of 2.55g of LOWINOXTM 22IB46 and 5.95g 2-butanone.
  • the emulsion layer was then doctor blade-coated at a blade setting of 100 ⁇ m with the protective layer coating composition to a wet layer thickness of 57 ⁇ m, which after drying for 8 minutes at 80°C on an aluminium plate in a drying cupboard produced a layer with the following composition: CAB 4.08g/m 2 PMMA 0.16g/m 2 Phthalazine 0.50g/m 2 4-methylphthalic acid 0.20g/m 2 tetrachlorophthalic acid 0.10g/m 2 tetrachlorophthalic acid anhydride 0.20g/m 2 LOWINOXTM 22IB46 2.55g/m 2
  • Sheets of the photosensitive thermally developable photographic material were information-wise exposed and thermally developed in an apparatus in which information-wise exposure and thermal development took place on the same heatable drum 198 mm in diameter and the photosensitive thermally developable photographic material was transported at a speed of 20.73 mm/s with its antistatic/antihalation-layer in contact with the drum i.e. with the protective layer for the silver behenate/silver halide emulsion layer outermost.
  • the optical densities of the resulting images were measured in transmission with a MacBethTM TR924 densitometer through a visible filter to produce a sensitometric curve for the photosensitive thermally developable photographic materials from which the maximum and minimum optical densities, D max and D min , and the relative photosensitivities for D min + 1.0 determined.
  • DRYVIEWTM photosensitive thermally developable photographic material from IMATION was used instead of the photosensitive thermally developable photographic material of COMPARATIVE EXAMPLE 1 and INVENTION EXAMPLES 1 to 4.
  • the DRYVIEWTM material is based on a conventional silver halide/silver behenate/reducing agent concept and is spectrally sensitized to infra-red radiation. Information-wise exposure and thermal processing were carried out using the apparatus used for COMPARATIVE EXAMPLE 1 and INVENTION EXAMPLES 1 to 4 with thermal development carried out at 123.9°C for 17.5 s instead of for 15 s at 121°C.

Description

Field of the invention
The present invention relates to a sensitivity-increasing recording process for photographic materials in which information-wise exposure is carried out during heating.
Background of the invention.
Thermal imaging or thermography is a recording process wherein images are generated by the use of imagewise modulated thermal energy.
In thermography three approaches are known:
  • 1. Image-wise or information-wise transfer of an ingredient necessary for the chemical or physical process bringing about changes in colour or optical density to a receptor element.
  • 2. Thermal dye transfer printing wherein a visible image pattern is formed by transfer of a coloured species from an imagewise heated donor element onto a receptor element.
  • 3. Direct thermal formation of a visible image pattern by image-wise or information-wise heating of a recording material containing matter that by chemical or physical process changes colour or optical density.
    • Thermographic materials of type 3 become photothermographic if a photosensitive agent is present which after exposure to UV, visible or IR light is capable of catalyzing or participating in a thermographic process bringing about changes in colour or optical density.
    Examples of photothermographic materials are the so called "Dry Silver"photothermographic materials of the 3M Company, which are reviewed by D.A. Morgan in "Handbook of Imaging Science", edited by A.R. Diamond, page 43, published by Marcel Dekker in 1991.
    DOS 2 248 545 discloses a copying process characterized in that the whole surface of a thermally developable photosensitive silver material is subjected before the complete execution of the exposure to a uniform auxiliary thermal treatment at a temperature, that is within the suitable development temperature range for the photosensitive material, and to thermal development after exposure; and that, in a subclaim, the photosensitive material can also be subjected to auxiliary heating during the exposure thereof. The specification and invention examples give no indication of the efficacity of auxiliary heating during exposure.
    JP-A-61 196243 discloses a scan type exposure and development installation having as distinctive feature that it has a rotation drum which has a thermal development photosensitive material wound around it and uses the axis center as rotation axis, an exposure head which is positioned opposite the circumference face of the rotation drum and moves in the axis direction of the rotation drum in response to the rotation of the rotation drum, and a heating head which is positioned opposite the circumference face of the rotation drum and moves in the axis direction of the rotation drum in response to the rotation of the rotation drum. The thermal heating head can be a laser heating head and heating development may be carried out while scanning the thermal development photosensitive material and as a result development and exposure may be carried out with the same installation at almost the same time thereby shortening the total treatment time of exposure and development.
    Yu. E. Usanov, T. B. Kolesova, L. P. Burleva, M. R. V. Sahyun and D. R. Whitcomb in the preprints of the Society for Imaging Science and Technology (I.S.& T.) 50th Annual Conference held at Cambridge, Massachusetts, USA between the 18th and 23rd May 1997, pages 42 to 45 reported that: Experiments carried out with thermally developed Dry Silver™ type 7858 photothermographic materials from 3M and spectrally sensitized model photothermo-graphic materials showed that preheating at temperatures higher than 100°C followed by cooling prior to flash lamp or sensitometer exposure results in decreased speed during development. Consequently, a decrease in the photosensitivity was observed. Analogous results were also obtained if the materials were exposed during the preheating process. The higher the pre-heating temperature above 100°C and the longer the time of preheating, the lower the material photosensitivity. It was determined that this phenomenon depends neither on the composition of the silver halides nor on the method of incorporating them into the thermally developable composition.
    It is desirable to increase the photosensitivity of photosensitive thermally developable photographic materials to be able to use less powerful heat sources. It is also desirable to achieve such an increase in photosensitivity, while enabling the simplification of photothermographic processing equipment, for example as disclosed in DE-A 196 36 235.0.
    Objects of the Invention
    It is therefore an object of the present invention to provide a method of increasing the photosensitivity of photosensitive thermally developable photographic materials.
    It is a further object of the present invention to provide an improved recording process enabling an increase in sensitivity, while enabling the use of simplified photothermographic processing equipment.
    Other objects and advantages of the present invention will become clear from the further description and examples.
    Summary of the Invention
    A recording process is provided comprising the steps of:
    information-wise exposing to radiation a photosensitive thermally developable photographic material, thereby producing a latent image; and heating the photosensitive thermally developable photographic material, characterized in that the photosensitive thermally developable photographic material is on one and the same holding or guiding means during both the information-wise exposure step and the heating step; the information-wise exposure step is carried out pixelwise during the heating step; the exposure step begins after the start of the heating step; and the duration of the exposure step is less than one tenth of the duration of the heating step.
    A method of increasing the photosensitivity of a photosensitive thermally developable photographic material is provided, characterized in that the photosensitive thermally developable photographic material is on one and the same holding or guiding means during both the information-wise exposure step and the heating step; the information-wise exposure step is carried out pixelwise during said heating step; the exposure step begins after the start of the heating step; and the duration of said exposure step is less than one tenth of the duration of the heating step.
    Preferred embodiments of the present invention are disclosed in the detailed description of the invention.
    Detailed Description of the Invention
    The inventors of the present invention surprisingly have found that the preheating of materials resulted in thermally developable photographic materials requiring shorter exposure times than with prior art processes in which unheated materials are exposed to recording radiation. This showed that materials upon heating are more sensitive to recording radiation and enables the apparatus to be simplified.
    However, upon prolonged preheating the sensitivity to wavelengths to which the photosensitive thermally developable photographic materials had been spectrally sensitized is reduced and in the case of some materials destroyed altogether, in all cases the UV-photosensitivity, i.e. intrinsic photosensitivity, of the materials remaining substantially unchanged. This indicates an inability of the spectral sensitizer alone or together with a supersensitizer to sensitize the materials to IR-radiation after prolonged preheating, for whatever reason.
    Recording process for and method of increasing photosensitivity of photosensitive thermally developable photographic materials
    According to the present invention it is preferred that the duration of the exposure step be less than one hundredth of the duration of the heating step.
    In a particular embodiment of the present invention thermal development of the photosensitive thermally developable photographic material is carried out during the heating step, during which a visible image is produced from the latent image resulting from the exposure step.
    In a particularly preferred embodiment of the present invention the heating step begins before the start of the exposure step and ends after thermal development to produce a visible image is complete.
    Photographic materials and photosensitive thermally developable photographic materials may, according to the present invention, be exposed with radiation of wavelength between an X-ray wavelength and a 5 microns wavelength with the image being obtained by pixel-wise exposure with a finely focused light source, such as a CRT light source; a UV, visible or IR wavelength laser, such as a He/Ne-laser or an IR-laser diode, e.g. emitting at 780nm, 830nm or 850nm; or a light emitting diode, for example one emitting at 659nm. Exposure with infra-red light or visible light is preferred, visible light in the wavelength range 600nm to 700nm being particularly preferred. Exposure with an infra-red emitting laser diode is preferred, according to the present invention.
    The photosensitive thermally developable photographic material may be heated during the exposure and the heating subsequent to the exposure by the same heating means. Furthermore, the photosensitive thermally developable photographic material may be heated prior to the exposure, during the exposure and during the heating subsequent to the exposure by the same heating means. A heated drum is a preferred common heating means.
    For the thermal development of information-wise exposed photosensitive thermally developable photographic materials, according to the recording process of the present invention, any sort of heat source can be used that enables the recording materials to be uniformly heated to the development temperature in a time acceptable for the application concerned e.g. contact heating with for example a heated roller, a heated drum, a thermal head, radiative heating, microwave heating etc. The preferred temperature of the photosensitive thermally developable photographic material during thermal development is between 110°C and 130°C.
    In a preferred recording process, according to the present invention, at least two radiation beams move simultaneously over the photosensitive thermally developable photographic material the first of the radiation beams carrying out the information-wise exposing of the photosensitive thermally developable photographic material and the second of which heats the information-wise exposed photosensitive thermally developable photographic material to a uniform development temperature.
    Photosensitive thermally developable photographic material
    The photosensitive thermally developable photographic material preferably contains an infrared sensitizer or a visible light sensitizer and particularly preferably further contains photosensitive silver halide, an organic reducing agent and a binder. The use in the present invention of a photosensitive thermally developable photographic material including a gelatinous silver halide emulsion layer is preferred. The use in the present invention of a photosensitive thermally developable photographic material further containing a substantially light-insensitive organic silver salt with which the photosensitive silver halide in catalytic association and an organic reducing agent for the substantially light-insensitive organic silver salt in thermal working relationship therewith is particularly preferred. The photosensitive thermally developable photographic material may have a layer system in which the ingredients are dispersed in different layers, with the proviso that the image-forming process can take place.
    For example, in the case of photosensitive thermally developable photographic materials containing photosensitive silver halide and an organic reducing agent optionally further containing a substantially light-insensitive organic silver salt, the photosensitive silver halide or substantially light-insensitive organic silver salt, if present, must be in thermal working relationship with the organic reducing agent i.e. during the thermal development process the reducing agent must be present in such a way that it is able to diffuse to the photosensitive silver halide or the substantially light-insensitive organic silver salt particles so that reduction of the silver halide or organic silver salt can take place; and the photosensitive silver halide is in catalytic association with the substantially light-insensitive organic silver salt, if present.
    Photosensitive silver halide
    The photosensitive silver halide used in the present invention may be employed in a range of 0.1 to 100 mol percent; preferably, from 0.2 to 80 mol percent; particularly preferably from 0.3 to 50 mol percent; especially preferably from 0.5 to 35 mol %; and especially from 1 to 12 mol % of substantially light-insensitive organic silver salt.
    The silver halide may be any photosensitive silver halide such as silver bromide, silver iodide, silver chloride, silver bromoiodide, silver chlorobromoiodide, silver chlorobromide etc. The silver halide may be in any form which is photosensitive including, but not limited to, cubic, orthorhombic, tabular, tetrahedral, octagonal etc. and may have epitaxial growth of crystals thereon.
    The silver halide used in the present invention may be employed without modification. However, it may be chemically sensitized with a chemical sensitizing agent such as a compound containing sulphur, selenium, tellurium etc., or a compound containing gold, platinum, palladium, iron, ruthenium, rhodium or iridium etc., a reducing agent such as a tin halide etc., or a combination thereof. The details of these procedures are described in T.H. James, "The Theory of the Photographic Process", Fourth Edition, Macmillan Publishing Co. Inc., New York (1977), Chapter 5, pages 149 to 169.
    Spectral sensitizer
    The photosensitive thermally developable photographic material, according to the present invention, may contain an infra-red sensitizer or a visible light sensitizer. Suitable sensitizers include cyanine, merocyanine, styryl, hemicyanine, oxonol, hemioxonol and xanthene dyes. Useful cyanine dyes include those having a basic nucleus, for example a thiazoline nucleus, an oxazoline nucleus, a pyrroline nucleus, a pyridine nucleus, an oxazole nucleus, a thiazole nucleus, a selenazole nucleus and an imidazole nucleus. Preferred merocyanine dyes include those having not only the above described basic nuclei but also acid nuclei, for example a thiohydantoin nucleus, a rhodanine nucleus, an oxazolidinedione nucleus, a thiazolidinedione nucleus, a barbituric acid nucleus, a thiazolinone nucleus, a malononitrile nucleus and a pyrazolone nucleus. Of the above described cyanine and merocyanine dyes, those having imino groups or carboxyl groups are particularly preferred.
    Suitable infra-red sensitizers include those disclosed in EP-A's 465 078, 559 101, 616 014 and 635 756, JN's 03-080251, 03-163440, 05-019432, 05-072662 and 06-003763 and US-P's 4,515,888, 4,639,414, 4,713,316, 5,258,282 and 5,441,866.
    Infra-red sensitizers according to general formula (I) are especially preferred for use in the photosensitive thermally-developable photographic material used in the present invention:
    Figure 00080001
    with an anion if necessary for charge compensation, wherein Z1 and Z2 independently represent S, O or Se; R1 and R13 independently represent an alkylene group; X1 and X2 independently represent a -(C=O)-R18, a (SO2)-R19 or a - (S=O) -R20 group where R18, R19 and R20 independently represent an alkoxy-, aryloxy-, amino- or substituted amino-group; R2, R3, R4, R5, R14, R15, R16 and R17 independently represent hydrogen, chlorine, bromine, fluorine, iodine or a keto-, sulfo-, carboxy-, ester-, sulfonamide-, amide-, dialkylamino-, nitro-, cyanoalkyl-, alkenyl-, hetero-aromatic, aryl-, alkoxy- or aryloxy-group, which groups may be substituted; or each of R2 together with R3, R3 together with R4, R4 together with R5, R14 together with R15, R15 together with R16 and R16 together with R17 may independently constitute the atoms necessary to complete a benzene ring which may be substituted; R6, R7, R8, R9, R10, R11 and R12 independently represent hydrogen, chlorine, bromine, fluorine, iodine, an alkyl group, a substituted alkyl group, an alkoxy group, an aryloxy group, a thioalkyl group, a disubstituted amino group, where the substituents may constitute the atoms necessary to complete a 5-ring atom or 6ring atom heterocyclic ring, or each of R6 together with R8, R8 together with R10, R10 together with R12, R7 together with R9 and R9 together with R11 may independently constitute the atoms necessary to complete a 5-atom or 6-atom carbocylic or heterocyclic ring which may be substituted; and each of R1 together with R6 and R13 together with R12 may independently constitute the atoms necessary to complete a 5-ring atom or 6-ring atom heterocyclic ring which may be substituted. In the general formula (I) the substituted amino group represented by the R18, R19 and R20 groups may be all possible substitutions of the amino group, including thereby, -NH- (C=O)-R21, -NH-(SO2)-R22, -NH-(S=O)-R23.
    -N'-CN, -N-(C=O)-R24, -N-(SO2)-R25, -N-(S=O)-R26 and -N -CN groups where R21, R22, R23, R24, R25 and R26 independently represent an alkl, substituted alkyl, aryl or a substituted aryl group.
    In particularly preferred dyes corresponding to general formula (I), used according to the present invention, R18, R19 and R20 independently represent a -NH-(C=O)-R21, -NH-(SO2)-R22, -NH-(S=0)-R23 or a -NH-CN group which may be deprotonated, where R21, R22 and R23 independently represent an alkyl, substituted alkyl, aryl or substituted aryl group.
    IR-sensitizing dyes according to general formula (I) suitable for use according to the present invention are:
    Figure 00100001
    Figure 00100002
    Figure 00110001
    Figure 00110002
    Figure 00120001
    Figure 00120002
    Figure 00130001
    Figure 00130002
    Figure 00140001
    Figure 00140002
    Figure 00150001
    Supersensitizers
    According to the present invention the photosensitive thermally developable photographic material further includes a supersensitizer. Preferred supersensitzers are selected from the group of compounds consisting of: mercapto-compounds, disulfide-compounds, stilbene compounds, organoborate compounds and styryl compounds. Suitable supersensitizers for use with infra-red spectral sensitizers are disclosed in EP-A 559 228, EP-A 587 338, US-P 3,877,943, US-P 4,873,184 and unpublished European Patent Application EP 96202107.7.
    Substantially light-insensitive organic silver salts
    Preferred substantially light-insensitive organic silver salts used in the photosensitive thermally developable photographic material used in the present invention are silver salts of aliphatic carboxylic acids known as fatty acids, wherein the aliphatic carbon chain has preferably at least 12 C-atoms, e.g. silver laurate, silver palmitate, silver stearate, silver hydroxystearate, silver oleate and silver behenate, which silver salts are also called "silver soaps"; silver dodecyl sulphonate described in US-P 4,504,575; and silver di-(2-ethylhexyl)-sulfosuccinate described in EP-A 227 141. Modified aliphatic carboxylic acids with thioether group as described e.g. in GB-P 1,111,492 and other organic silver salts as described in GB-P 1,439,478, e.g. silver benzoate and silver phthalazinone, may be used likewise to produce a thermosensitive silver image. Silver imidazolates and the substantially light-insensitive inorganic or organic silver salt complexes described in US-P 4,260,677 are also suitable.
    The term substantially light-insensitive organic silver salt for the purposes of the present invention also includes mixtures of organic silver salts.
    Emulsion of organic silver salt and photosensitive silver halide
    The silver halide may be added to the photosensitive thermally developable photographic material in any fashion which places it in catalytic proximity to the substantially light-insensitive organic silver salt. Photosensitive silver halide and substantially light-insensitive organic silver salt which are separately formed, i.e. ex-situ or "preformed", in a binder can be mixed prior to use to prepare a coating solution, but they may be blended for a long period of time prior to use. A particularly preferred mode of preparing the emulsion of organic silver salt and photosensitive silver halide for coating of the photosensitive thermally developable photographic material from solvent media, according to the present invention is that disclosed in US-P 3,839,049, but other methods such as those described in Research Disclosure, June 1978, item 17029 and US-P 3,700,458 may also be used.
    Organic reducing agent
    Suitable organic reducing agents for use in the photosensitive thermally developable photographic material used in the present invention are organic compounds containing at least one active hydrogen atom linked to 0, N or C, such as is the case with, mono-, bis-, tris- or tetrakis-phenols; mono- or bis-naphthols; di- or polyhydroxy-naphthalenes; di- or polyhydroxybenzenes; hydroxymonoethers such as alkoxynaphthols, e.g. 4-methoxy-1-naphthol described in US-P 3,094,41; pyrazolidin-3-one type reducing agents, e.g. PHENIDONE™; pyrazolin-5-ones; indan-1,3-dione derivatives; hydroxytetrone acids; hydroxytetronimides; 3-pyrazolines; pyrazolones; reducing saccharides; aminophenols e.g. METOL™; p-phenylenediamines, hydroxylamine derivatives such as for example described in US-P 4,082,901; reductones e.g. ascorbic acids; hydroxamic acids; hydrazine derivatives; amidoximes; n-hydroxyureas; and the like, see also US-P 3,074,809, 3,080,254, 3,094,417 and 3,887,378. Particularly preferred catechol-type reducing agents are described in EP-A 692 733 and EP-A 599 369.
    Polyphenols such as the bisphenols used in the 3M Dry Silver™ materials, sulfonamide phenols such as used in the Kodak Dacomatic™ materials, and naphthols are particularly preferred for photosensitive thermally developable photographic materials on the basis of silver halide/organic silver salt/reducing agent.
    Auxiliary reducing agents
    The above mentioned reducing agents being considered as primary or main reducing agents may be used in conjunction with so-called auxiliary reducing agents. Auxiliary reducing agents that may be used in conjunction with the above-mentioned primary reducing agents are sulfonamidophenols as described in the periodical Research Disclosure, February 1979, item 17842, in US-P 4,360,581 and 4,782,004, and in EP-A 423 891. Other auxiliary reducing agents that may be used in conjunction with the above mentioned primary reducing agents are hydrazides such as disclosed in EP-A 762 196, sulfonyl hydrazide reducing agents such as disclosed in US-P 5,464,738; trityl hydrazides and formyl-phenyl-hydrazides such as disclosed in US-P 5,496,695; trityl hydrazides and formyl-phenyl-hydrazides with diverse auxiliary reducing agents such as disclosed in US-P 5,545,505, US-P 5.545.507 and US-P 5,558,983; acrylonitrile compounds as disclosed in US-P 5,545,515 and US-P 5,635,339; and organic reducing metal salts, e.g. stannous stearate described in US-P 3,460,946 and 3,547,648.
    Binder
    The binder for the photosensitive thermally developable photographic material used in the present invention may be coatable from a solvent or aqueous dispersion and must themselves be film-forming or must be used in association with a film-forming binder.
    Film-forming binders coatable from a solvent dispersion and usable in the present invention may be all kinds of natural, modified natural or synthetic resins or mixtures of such resins, wherein the organic silver salt can be dispersed homogeneously: e.g. polyurethanes, polyesters, polyamides, polycarbonates and polymers derived from α,β-ethylenically unsaturated compounds, polyvinyl acetals preferably polyvinylbutyral, and homopolymers and copolymers produced using monomers selected from the group consisting of: acrylonitrile, acrylamides, methacrylamides. methacrylates, acrylates, methacrylic acids, acrylic acids, vinyl esters, styrenes and alkenes; or mixtures thereof.
    The film-forming binder coatable from an aqueous dispersion used in the present invention may be all kinds of transparent or translucent water-dispersible or water soluble natural, modified natural or synthetic resins or mixtures of such resins, wherein the organic silver salt can be dispersed homogeneously for example proteins, such as gelatin and gelatin derivatives ; cellulose derivatives; polysaccharides; galactomannan; polyvinyl alcohol; polyvinylpyrrolidone; polyurethanes; polyesters; polyamides; polycarbonates; polymers derived from α,β-ethylenically unsaturated compounds, for example polyvinyl acetals, preferably polyvinylbutyral, and homopolymers and copolymers produced using monomers selected from the group consisting of: acrylonitrile, acrylamides, methacrylamides. methacrylates, acrylates, methacrylic acids, acrylic acids, vinyl esters, styrenes and alkenes; and latexes of water dispersible polymers, with or without hydrophilic groups, or mixtures thereof.
    The above-mentioned binders or mixtures thereof may be used in conjunction with waxes or "heat solvents" also called "thermal solvents" or "thermosolvents" improving the reaction speed of the redox-reaction at elevated temperature.
    Polycarboxylic acids and anhydrides thereof
    The photosensitive thermally developable photographic material used according to the present invention may also contain at least one polycarboxylic acid and/or anhydride thereof in a molar percentage of at least 20 with respect to all the organic silver salt(s) present and in thermal working relationship therewith. Preferred aromatic polycarboxylic acids are ortho-phthalic acid and 3-nitro-phthalic acid, tetrachlorophthalic acid, mellitic acid, pyromellitic acid and trimellitic acid and the anhydrides thereof.
    Toning agents
    In order to obtain a neutral black image tone in the higher densities and neutral grey in the lower densities the photosensitive thermally developable photographic material preferably contains in admixture with the organic silver salts and reducing agents a so-called toning agent known from thermography or photothermography. Suitable toning agents are succinimide, phthalazine and the phthalimides and phthalazinones within the scope of the general formulae described in US-P 4,082,901 and the toning agents described in US-P 3,074,809, 3,446,648 and 3,844,797. Particularly useful toning agents are the heterocyclic toner compounds of the benzoxazine dione or naphthoxazine dione type as described in GB-P 1,439,478, US-P 3,951,660 and US-P 5,599,647.
    Antihalation dyes
    In addition to the ingredients, the photosensitive thermally developable photographic materials used in the present invention may also contain antihalation or acutance dyes which absorb light which has passed through the photosensitive thermally developable photographic material, thereby preventing its reflection. Such dyes may be incorporated into the photosensitive thermally developable photographic material or in any other layer of the photographic material of the present invention.
    Other additives
    In addition to the ingredients the photosensitive thermally developable photographic material used in the present invention may also contain additives such as free fatty acids, surface-active agents, silicone oil, e.g. BAYSILONE™ Öl A (from BAYER AG, GERMANY) ; ultraviolet light absorbing compounds; silica; colloidal silica; fine polymeric particles, e.g. of poly(methylmethacrylate); and/or optical brightening agents.
    Support
    The support for the photosensitive thermally developable photographic material used in the present invention may be transparent, translucent or opaque, e.g. having a white light reflecting aspect and is preferably a thin flexible carrier made e.g. from paper, polyethene coated paper or transparent resin material, e.g. made of a cellulose ester, e.g. cellulose triacetate, corona and flame treated polypropylene, polystyrene, polymethacrylic acid ester, polycarbonate or polyester, e.g. polyethylene terephthalate or polyethylene naphthalate as disclosed in GB 1,293,676, GB 1,441,304 and GB 1,454,956.
    The support may be in sheet, ribbon or web form and subbed if need be to improve the adherence to the thereon coated thermosensitive recording layer. One or more backing layers may be provided to control physical properties such as curl or static.
    Protective layer
    The outermost layer of the side of the photosensitive thermally developable photographic material which is photosensitive may be a protective layer to avoid local deformation of the photosensitive thermally developable photographic material and to improve resistance against abrasion.
    The protective layer preferably comprises a binder, which may be hydrophobic (solvent soluble) or hydrophilic (water soluble) e.g. as described in EP-A 614 769. Hydrophilic binders are, however, preferred for the protective layer, as coating can be performed from an aqueous composition and mixing of the hydrophilic protective layer with the immediate underlayer can be avoided by using a hydrophobic binder in the immediate underlayer.
    A protective layer used in the present invention may also contain at least one solid lubricant having a melting point below 150°C and at least one liquid lubricant at least one of these lubricants being a phosphoric acid derivative; and additional dissolved lubricating material and/or particulate material, e.g. talc particles, optionally protruding from the outermost layer. The lubricant may be applied with or without a polymeric binder.
    Such protective layers may also contain particulate material, e.g. talc particles, optionally protruding from the protective outermost layer as described in WO 94/11198. Other additives can also be incorporated therein e.g. colloidal particles such as colloidal silica.
    Antistatic layer
    The photosensitive thermally developable photographic materials used in the present invention may further include an antistatic layer. Suitable antistatic layers are described in EP-A's 444 326, 534 006 and 644 456, US-P's 5,364,752 and 5,472,832 and DOS 4125758. Particularly preferred antistatic layers are those based on polythiophene as disclosed in EP-A 628 560, US-P 5,354,613, US-P 5,372,924, US-P 5,370,981 and US-P 5,391,472.
    Coating
    The coating of any layer of the photosensitive thermally developable photographic materials used in the present invention may proceed by any thin-film coating technique known in the art. In the coating of web type supports for photographic materials slide hopper coating is preferred, but other coating techniques such as dip coating and air knife coating may also be used. Details about such coating techniques can be found in "Modern Coating and Drying Technology" by Edward D. Cohen and Edgar B. Gutoff, published by VCH Publishers, Inc. 220 East 23rd Street, Suite 909 New York, NY 10010.
    Industrial application
    The photosensitive thermally developable photographic materials used in the present invention can be used for both the production of transparencies and reflection type prints. This means that the support will be transparent or opaque, e.g. having a white light reflecting aspect. For example, a paper base substrate is present which may contain white reflecting pigments, optionally also applied in an interlayer between the recording material and the paper base substrate. Should a transparent base be used, the base may be colourless or coloured, e.g. has a blue colour.
    In the graphics hard copy field photosensitive thermally developable photographic materials on a white opaque base are used, whereas in the medical diagnostic field black-imaged transparencies are widely used in inspection techniques operating with a light box.
    The following ingredients were used in the INVENTION & COMPARATIVE EXAMPLES of the present invention:
  • a) antihalation/antistatic layer ingredients:
    D01:
    Figure 00220001
    KELZAN™ S:
    a xanthan gum from MERCK & CO., Kelco Division, USA, which according to Technical Bulletin DB-19 is a polysaccharide containing mannose, glucose and glucuronic repeating units as a mixed potassium, sodium and calcium salt;
    PT-dispersion:
    a dispersion of poly(3,4-ethylenedioxythiophene)/ polystyrene sulphonic acid produced by the polymerization of 3,4-ethylenedioxy-thiophene in the presence of polystyrene sulphonic acid and ferric sulphate as described in US-P 5,354,613;
    ULTRAUON™ W:
    an aryl sulfonate from CIBA-GEIGY;
    PERAPRET™ PE40:
    a 40% aqueous dispersion of polyethylene wax from BASF;
    KIESELSOL™ 100F:
    a 36% aqueous dispersion of colloidal silica from BAYER;
    MAT01:
    20% aqueous dispersion of particles of methylmethacrylate(98% by weight)-stearylmethacrylate(2% by weight)-copolymeric beads with an average particle size of 5.9µm as described in US-P 4,861,812;
    LATEX01:
    a 12% by weight dispersion of polymethylmethacrylate with an average particle size of 88.8nm as described in US-P 5,354,613;
  • b) photosensitive layer:
  • i) silver behenate/silver halide emulsion layer:
    GEL:
    phthaloylgelatin, type 16875 from ROUSSELOT;
    Butvar™ B76:
    polyvinylbutyral from MONSANTO;
    LOWINOX™ 22IB46:
    2-propyl-bis(2-hydroxy-3,5-dimethylphenyl)methane from CHEM. WERKE LOWI;
    TMABP:
    tetramethylammonium bromide perbromide;
    TMPS:
    tribromomethyl benzenesulfinate;
    MBI:
    2-mercaptobenzimidazole;
    SENSI:
    SENSI 01
  • ii) protective layer:
    CAB:
    cellulose acetate butyrate, CAB-171-15S from EASTMAN;
    PMMA:
    polymethylmethacrylate, Acryloid™ K120N from ROHM & HAAS.
    LOWINOX™ 22IB46:
    2-propyl-bis(2-hydroxy-3,5-dimethylphenyl)methane from CHEM. WERKE LOWI;
    • The following examples illustrate the present invention without however limiting it thereto. All percentages, parts and ratios are by weight unless otherwise mentioned.
    COMPARATIVE EXAMPLE 1 & INVENTION EXAMPLES 1 to 4 Photosensitive thermally developable photographic materials Support
    A polyethylene terephthalate (PET) foil pigmented with a blue pigment was first coated on both sides with a subbing layer consisting of a terpolymer latex of vinylidene chloride-methyl acrylate-itaconic acid (88/10/2) in admixture with colloidal silica (surface area 100m2/g). After stretching the foil in the transverse direction the foil had a thickness of 175µm with coverages of the terpolymer and of the silica in the subbing layers of 170mg/m2 and 40mg/m2 respectively on each side of the PET-foil.
    Antihalation/antistatic layer
    The antihalation/antistatic layer was prepared by first adsorbing antihalation dye D01 onto the polymethyl methacrylate particles of LATEX01 by adding 55mg of D01 dissolved in ethyl acetate/g polymethyl methacrylate and then evaporating off the ethyl acetate.
    One side of the thus subbed PET-foil was then coated with an antistatic composition obtained by dissolving 0.30g of KELZAN™ S in a stirred mixture of 22.4mL of N-methylpyrrolidone, 0.84g of ULTRAVON™ W, 1g of PERAPRET™ PE40 and 2.22g of KIESELSOL 100F in 74.3mL of deionized water and then adding with stirring: 0.2mL of 25% NH4OH, 0.6g of dried PT-dispersion, 66.7mL of LATEX01 after adsorption of D01, 1.2mL of MAT01 and 30mL of 2-propanol to produce a layer after drying at 120°C consisting of:
    KELZAN™ S 7.5mg/m2
    Dried PT-dispersion 15 mg/m2
    ULTRAVON™ W 21 mg/m2
    polyethylene wax (from PERAPRET™ PE40) 10 mg/m2
    colloidal silica (from KIESELSOL™ 100F) 20 mg/m2
    5.9µm beads of crosslinked methylmethacrylate-stearylmethacrylate copolymer (from MAT01) 6 mg/m2
    polymethylmethacrylate (from LATEX01) 200 mg/m2
    Antihalation dye D01 11 mg/m2
    Silver halide emulsion
    A silver halide emulsion consisting of 3.11% by weight of silver halide particles consisting of 97mol% silver bromide and 3mol% silver iodide with a weight average particle size of 50nm, 0.47% by weight of GEL as dispersing agent in deionized water was prepared using conventional silver halide preparation techniques such as described, for example, in T.H. James, "The Theory of the Photographic Process", Fourth Edition, Macmillan Publishing Co. Inc., New York (1977), Chapter 3, pages 88-104.
    Silver behenate/silver halide emulsion
    The silver behenate/silver halide emulsion was prepared by adding a solution of 6.8kg of behenic acid in 67L of 2-propanol at 65°C to a 400L vessel heated to maintain the temperature of the contents at 65°C, converting 96% of the behenic acid to sodium behenate by adding with stirring 76.8L of 0.25M sodium hydroxide in deionized water, then adding with stirring 10.5kg of the above-described silver halide emulsion at 40°C and finally adding with stirring 48L of a 0.4M solution of silver nitrate in deionized water. Upon completion of the addition of silver nitrate the contents of the vessel were allowed to cool and the precipitate filtered off, washed, slurried with water, filtered again and finally dried at 40°C for 72 hours.
    7kg of the dried powder containing 9mol% silver halide and 4mol% behenic acid with respect to silver behenate were then dispersed in a solution of 700g of Butvar™ B76 in 15.6kg of 2-butanone using conventional dispersion techniques yielding a 33% by weight dispersion. 7.4kg of 2-butanone were then added and the resulting dispersion homogenized in a microfluidizer. Finally 2.8kg of Butvar™ B76 were added with stirring to produce a dispersion with 31% by weight of solids.
    Coating and drying of silver behenate/silver halide emulsion layer
    The emulsion layer coating composition for the photosensitive thermally developable photographic material was prepared by adding the following solutions or liquids to 40.86g of the above-mentioned silver behenate/silver halide emulsion in the following sequence with stirring: 10.87g of 2-butanone, 0.75g of a 9% solution of TMABP in methanol followed by 2 hours stirring, 1.3g of 2-butanone, 0.2g of a 11% solution of calcium bromide in methanol and 1.3g of 2-butanone followed by 30 minutes stirring, a solution consisting of 0.21g of LOWINOX™ 22IB46, 0.5g of TMPS and 9.24g of 2-butanone followed by 10 minutes stirring, 1.84g of a 0.11% methanol solution of SENSI followed by 30 minutes stirring and finally 4.35g of Butvar™ B76 were added followed by 45 minutes of stirring and then 4.79g of 2-butanone.
    The PET-support subbed and coated with an antihalation/antistatic layer as described above was then doctor blade-coated at a blade setting of 150µm on the side of the support not coated with a backside layer with the coating composition to a wet layer thickness of 80µm followed by drying for 5 minutes at 80°C on an aluminium plate in a drying cupboard.
    Protective layer
    A protective layer coating composition for the photosensitive thermally developable photographic material was prepared by dissolving 4.08g of CAB and 0.16g of PMMA in 36.3g of 2-butanone and 4.16g of methanol adding the following solids or solution with stirring in the following sequence: 0.5g of phthalazine, 0.2g of 4-methylphthalic acid, 0.1g of tetrachlorophthalic acid, 0.2g of tetrachlorophthalic acid anhydride and a solution consisting of 2.55g of LOWINOX™ 22IB46 and 5.95g 2-butanone. The emulsion layer was then doctor blade-coated at a blade setting of 100µm with the protective layer coating composition to a wet layer thickness of 57µm, which after drying for 8 minutes at 80°C on an aluminium plate in a drying cupboard produced a layer with the following composition:
    CAB 4.08g/m2
    PMMA 0.16g/m2
    Phthalazine 0.50g/m2
    4-methylphthalic acid 0.20g/m2
    tetrachlorophthalic acid 0.10g/m2
    tetrachlorophthalic acid anhydride 0.20g/m2
    LOWINOX™ 22IB46 2.55g/m2
    Information-wise exposure and thermal processing
    Sheets of the photosensitive thermally developable photographic material were information-wise exposed and thermally developed in an apparatus in which information-wise exposure and thermal development took place on the same heatable drum 198 mm in diameter and the photosensitive thermally developable photographic material was transported at a speed of 20.73 mm/s with its antistatic/antihalation-layer in contact with the drum i.e. with the protective layer for the silver behenate/silver halide emulsion layer outermost. Information-wise exposure took place with a 200mW laser diode from SDL at a speed of 20.73 mm/s at 10.85 lines/mm with a maximum laser intensity of 71 mW/spot (diameter 120µm), each 355.6 x 431.8 mm2 sheet requiring 20.8 s for exposure. Thermal development was carried out for 15 s at 121°C, the sheet being in contact with the heatable drum over 311.02 mm of the circumference thereof. For COMPARATIVE EXAMPLE 1, the sheet was neither heated before nor during exposure and for INVENTION EXAMPLES 1 to 4 the sheets were preheated via the drum for different times and heated during exposure.
    The optical densities of the resulting images were measured in transmission with a MacBeth™ TR924 densitometer through a visible filter to produce a sensitometric curve for the photosensitive thermally developable photographic materials from which the maximum and minimum optical densities, Dmax and Dmin, and the relative photosensitivities for Dmin + 1.0 determined.
    The Dmax- and Dmin-values and the relative photosensitivity values to obtain an optical density of Dmin + 1.0 obtained upon information-wise exposure and thermal processing of the photosensitive thermally developable photographic material together with the preheating conditions and thermal processing conditions used are summarized in table 1.
    Comparative example number preheating thermal processing conditions D max D min Relative photosensitivity at D min + 1.0 [J/m 2 ]
    temperature [°C] time [s] temperature [°C] time [s]
    1 - - 121 15 2.34 0.32 1.05
    Invention example number preheating thermal processing conditions D max D min Relative photosensitivity at D min + 1.0 [J/m 2 ]
    temperature [°C] time [s] temperature [°C] time [s]
    1 121 0.52 121 15 2.50 0.32 0.92
    2 121 1.56 121 15 2.56 0.32 0.71
    3 121 2.60 121 15 2.78 0.32 0.71
    4 121 3.64 121 15 3.00 0.32 0.52
    A comparison of the photosensitivities attained upon heating during exposure with different preheating conditions compared with the results obtained with the COMPARATIVE EXAMPLE 1 for which exposure took place with a cold material and no preheating was carried out show a pronounced increase in Dmax for the same exposure and a significant increase in photosensitivity. Furthermore, this increase in photosensitivity was achieved with exposure taking place during heating with the photosensitive thermally developable photographic material on one and the same holding or guiding means, in this instance a drum, thereby enabling a more compact processing unit to be used.
    COMPARATIVE EXAMPLE 2 & INVENTION EXAMPLE 5
    In INVENTION EXAMPLE 5 DRYVIEW™ photosensitive thermally developable photographic material from IMATION was used instead of the photosensitive thermally developable photographic material of COMPARATIVE EXAMPLE 1 and INVENTION EXAMPLES 1 to 4. The DRYVIEW™ material is based on a conventional silver halide/silver behenate/reducing agent concept and is spectrally sensitized to infra-red radiation. Information-wise exposure and thermal processing were carried out using the apparatus used for COMPARATIVE EXAMPLE 1 and INVENTION EXAMPLES 1 to 4 with thermal development carried out at 123.9°C for 17.5 s instead of for 15 s at 121°C.
    The Dmax- and Dmin-values and the relative photosensitivity values to obtain an optical density of Dmin + 1.0 obtained upon information-wise exposure and thermal processing of the photosensitive thermally developable photographic material together with the preheating conditions and thermal processing conditions used are summarized in table 2.
    Comparative example number preheating thermal processing conditions Dmax Dmin Relative photosensitivity at Dmin + 1.0 [J/m2]
    temperature [°C] time [s] temperature [°C] time [s]
    2 - - 123.9 17.5 2.93 0.26 0.67
    Invention example number
    5 123.9 0.52 123.9 17.5 3.07 0.26 0.57
    A comparison of the photosensitivities attained upon heating during exposure with preheating compared with the results obtained with the COMPARATIVE EXAMPLE 2 for which exposure took place with a cold material and no preheating was carried out show an increase in Dmax for the same exposure and an increase in photosensitivity. Again, this increase in photosensitivity was achieved with exposure taking place during heating with the photosensitive thermally developable photographic material on one and the same holding or guiding means, in this instance a drum, thereby enabling a more compact processing unit to be used.
    Having described in detail preferred embodiments of the present invention, it will be now apparent to those skilled in the art that numerous modifications can be made therein without departing from the scope of the invention as defined in the following claims.

    Claims (10)

    1. A recording process comprising the steps of: information-wise exposing to radiation a photosensitive thermally developable photographic material, thereby producing a latent image; and heating said photosensitive thermally developable photographic material, characterized in that said photosensitive thermally developable photographic material is on one and the same holding or guiding means during both said information-wise exposure step and said heating step; said information-wise exposure step is carried out pixelwise during said heating step; said exposure step begins after the start of said heating step; and the duration of said exposure step is less than one tenth of the duration of said heating step.
    2. Recording process according to claim 1, wherein thermal development of said photosensitive thermally developable photographic material is carried out during said heating step.
    3. Recording process according to claim 1 or 2, wherein the duration of said exposure step is less than one hundredth of the duration of said heating step.
    4. Recording process according to any of the preceding claims, wherein said photosensitive thermally developable photographic material contains an infra-red sensitizer.
    5. Recording process according to claim 4, wherein said infra-red sensitizer is represented by general formula (I):
      Figure 00300001
      with an anion if necessary for charge compensation, wherein Z1 and Z2 independently represent S, O or Se; R1 and R13 independently represent an alkylene group; X1 and X2 independently represent a -(C=O) -R18, a -(SO2)-R19 or a -(S=O)-R20 group where R18, R19 and R20 independently represent an alkoxy-, aryloxy-, amino- or substituted amino-group; R2, R3, R4, R5, R14, R15, R16 and R17 independently represent hydrogen, chlorine, bromine, fluorine, iodine or a keto-, sulfo-, carboxy-, ester-, sulfonamide-, amide-, dialkylamino-, nitro-, cyano-, alkyl-, alkenyl-, hetero-aromatic, aryl-, alkoxy- or aryloxy-group, which groups may be substituted; or each of R2 together with R3, R3 together with R4, R4 together with R5, R14 together with R15, R15 together with R16 and R16 together with R17 may independently constitute the atoms necessary to complete a benzene ring which may be substituted; R6, R7, R8, R9, R10, R11 and R12 independently represent hydrogen, chlorine, bromine, fluorine, iodine, an alkyl group, a substituted alkyl group, an alkoxy group, an aryloxy group, a thioalkyl group, a disubstituted amino group, where the substituents may constitute the atoms necessary to complete a 5-ring atom or 6-ring atom heterocyclic ring, or each of R6 together with R8, R8 together with R10, R10 together with R12, R7 together with R9 and R9 together with R11 may independently constitute the atoms necessary to complete a 5-atom or 6-atom carbocylic or heterocyclic ring which may be substituted; and each of R1 together with R6 and R13 together with R12 may independently constitute the atoms necessary to complete a 5-ring atom or 6-ring atom heterocyclic ring which may be substituted.
    6. Recording process according to any of claims 1 to 3, wherein said photosensitive thermally developable photographic material contains a visible light sensitizer.
    7. Recording process according to any of the preceding claims, wherein said photosensitive thermally developable photographic material further contains photosensitive silver halide, an organic reducing agent and a binder.
    8. Recording process according to any of the preceding claims, wherein said photosensitive thermally developable photographic material further contains a substantially light-insensitive organic silver salt.
    9. Recording process according to any of the preceding claims, wherein at least two radiation beams move simultaneously over said photosensitive thermally developable photographic material the first of said radiation beams carrying out said information-wise exposing of said photosensitive thermally developable photographic material and the second of which heats said information-wise exposed photosensitive thermally developable photographic material to a uniform development temperature.
    10. A method of increasing the photosensitivity of a photosensitive thermally developable photographic material, characterized in that said photosensitive thermally developable photographic material is on one and the same holding or guiding means during both said information-wise exposure step and said heating step; said information-wise exposure step is carried out pixelwise during said heating step; said exposure step begins after the start of said heating step; and the duration of said exposure step is less than one tenth of the duration of said heating step.
    EP97202521A 1996-09-06 1997-08-14 A sensitivity-increasing recording process for a photosensitive thermally developable photographic material Expired - Lifetime EP0836116B1 (en)

    Applications Claiming Priority (4)

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    US812450 1985-12-23
    DE19636235A DE19636235A1 (en) 1996-09-06 1996-09-06 Method and device for recording information on thermally developable photographic material
    DE19636235 1996-09-06
    US08/812,450 US5804355A (en) 1996-03-14 1997-03-06 Producing a contone image by sequentially exposing a thermo-sensitive imaging material by means of a set of radiation beams

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