EP1246001A1 - Thermographische Materialien und Aufzeichnungsverfahren dafür - Google Patents

Thermographische Materialien und Aufzeichnungsverfahren dafür Download PDF

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Publication number
EP1246001A1
EP1246001A1 EP01000097A EP01000097A EP1246001A1 EP 1246001 A1 EP1246001 A1 EP 1246001A1 EP 01000097 A EP01000097 A EP 01000097A EP 01000097 A EP01000097 A EP 01000097A EP 1246001 A1 EP1246001 A1 EP 1246001A1
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EP
European Patent Office
Prior art keywords
group
silver
recording material
thermographic
alkyl
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.)
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Application number
EP01000097A
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English (en)
French (fr)
Inventor
Horst Friedel
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.)
Agfa Gevaert NV
Agfa Gevaert AG
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Agfa Gevaert NV
Agfa Gevaert AG
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Publication date
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Priority to EP01000097A priority Critical patent/EP1246001A1/de
Priority to EP02100246A priority patent/EP1258775A3/de
Priority to US10/100,932 priority patent/US6686133B2/en
Publication of EP1246001A1 publication Critical patent/EP1246001A1/de
Withdrawn legal-status Critical Current

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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
    • G03C1/4989—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
    • 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
    • G03C1/49809—Organic silver compounds
    • 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
    • G03C2200/00—Details
    • G03C2200/42—Mixtures in general

Definitions

  • the present invention relates to thermographic recording materials and recording processes therefor.
  • Thermal imaging or thermography is a recording process wherein images are generated by the use of image-wise modulated thermal energy.
  • thermography three approaches are known:
  • Thermographic materials of type 3 can be rendered photothermographic by incorporating a photosensitive agent 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.
  • DE-OS 27 21 828 discloses a thermally developable light-sensitive material, consisting of a support, which contains thereon or in one or more layers at least (a) an organic silver salt, (b) a photocatalyst and (c) a reducing agent, wherein the organic silver salt (a) contains at least a silver salt with an uneven number of 21 or more carbon atoms; and examples with mixtures of two and three organic silver salts of monocarboxylic acids precipitated together, but all with 20 are more carbon atoms.
  • US-P 5,459,028 discloses a heat-developable photographic recording material comprising: (a) at least one binder layer coated on a support, said binder layer comprising at least one light-sensitive silver halide and a light-insensitive silver salt of a fatty acid; (b) at least one reducing agent; and (c) at least one auxiliary layer containing a developed image stabilizer selected from the group consisting of hexamethylene tetramine and salts thereof, triazaadamantane and salts thereof and compounds derived from hexamethylene tetramine wherein the compounds are derived from hexamethylene tetramine by exchanging one -CH 2 - group with -S-, -SO-, or -SO 2 -; (d) wherein said reducing agent and said developed image stabilizers are in a reactive relationship with the light-insensitive silver salt.
  • US-P 5,677,121 discloses a heat-developable silver halide infrared ray-sensitive material comprising a support having on one side of the support an emulsion layer containing a binder, a nonsensitive silver salt, a reducing agent for silver ion and silver halide grains spectrally sensitized at a wavelength within the region of from 750 to 1400nm, wherein the nonsensitive silver salt comprises a mixture of silver salts of at least three organic carboxylic acids, one of the acids is behenic acid, and the content of the behenic acid in the acids is from not less than 35 to less than 90 mol %.
  • EP-A 964 300 discloses a substantially light-insensitive black and white thermographic recording material having a support and a thermosensitive element containing a substantially light-insensitive organic silver salt, an organic reducing agent therefor in thermal working relationship therewith and a binder, characterized in that the thermosensitive element contains substantially light-insensitive mixed crystals of two or more silver salts of organic carboxylic acids with one or more carboxylic acid groups.
  • thermographic materials incorporating glutaric acid in the thermosensitive element have shown that, unlike substantially light-insensitive thermographic materials incorporating adipic acid or pimelic acid, silver glutarate could not be detected by X-ray diffraction spectroscopy during the thermal development process. Therefore there can be no question of incidental silver glutarate formation upon thermal development of substantially light-insensitive thermographic materials incorporating glutaric acid.
  • Thermographic recording materials are required which are thermally processable at lower temperatures to enable a higher throughput to be realized and which are capable of providing images with a higher gradation.
  • thermographic recording material with improved thermal developability without significant deterioration in other thermographic properties.
  • thermographic recording material capable of higher image gradation without significant deterioration in other thermographic properties.
  • thermo developability can be realized at lower temperatures without significant deterioration in other thermographic properties and images with higher gradation can be realized by using a mixture of particular substantially light-insensitive silver salts of monocarboxylic acids and particular light-insensitive silver salts of polycarboxylic acids. Particularly good results are obtained with a mixture of an equimolar mixture of silver glutarate and silver stearate.
  • thermographic recording process comprising the steps of: (i) providing a thermographic material as referred to above; (ii) bringing the side of the water resistant support with the thermosensitive element into contact with a thermal head; (iii) image-wise heating the thermographic material by pixel-wise heating with the thermal head under substantially water-free conditions; and (iv) removing the thermographic recording material from the thermal head.
  • thermothermographic recording material is also provided in an embodiment of the above-mentioned thermographic recording material in which the thermosensitive element further contains a photosensitive agent which after exposure to UV, visible or IR light is capable of catalyzing or participating in a thermographic process.
  • a photothermographic recording process comprising the steps of: (i) providing a photothermographic recording material as referred to above; (ii) image-wise exposing the photo-addressable thermosensitive element with actinic radiation; (iii) bringing the image-wise exposed photothermographic recording material into proximity with a heat source; (iv) uniformly heating the image-wise exposed photothermographic recording material under substantially water-free conditions; and (v) removing the photothermographic recording material from the source.
  • thermographic recording material includes photothermographic recording materials and substantially light-insensitive thermographic recording materials.
  • mixture of substantially light-insensitive silver salts of organic carboxylic acids includes a physical mixture of separately produced substantially light-insensitive silver salts of organic carboxylic acids, coprecipitated substantially light-insensitive silver salts of organic carboxylic acids and mixed crystals of substantially light-insensitive silver salts of organic carboxylic acids.
  • alkyl means all variants possible for each number of carbon atoms in the alkyl group i.e. for three carbon atoms: n-propyl and isopropyl; for four carbon atoms: n-butyl, isobutyl and tertiary-butyl; for five carbon atoms: n-pentyl, 1,1-dimethylpropyl, 2,2-dimethylpropyl and 2-methyl-butyl etc.
  • Gradation is the rate at which image density changes in response to heat in the case of substantially light-insensitive thermographic recording materials or in response to the logarithm of exposure in the case of photothermographic recording materials.
  • substantially light-insensitive is meant not intentionally light sensitive.
  • substantially water-free condition means heating at a temperature of 80 to 250°C.
  • substantially water-free condition means that the reaction system is approximately in equilibrium with water in the air, and water for inducing or promoting the reaction is not particularly or positively supplied from the exterior to the element. Such a condition is described in T.H. James, "The Theory of the Photographic Process", Fourth Edition, Macmillan 1977, page 374.
  • heat solvent in this invention is meant a nonhydrolyzable organic material which is in solid state in the recording layer at temperatures below 50°C but becomes a plasticizer for the recording layer in the heated region and/or liquid solvent for at least one of the redox-reactants, e.g. the reducing agent for the organic silver salt, at a temperature above 60°C.
  • thermographic recording material comprising a support and a thermosensitive element, the thermosensitive element containing a mixture of substantially light-insensitive silver salts of organic carboxylic acids with one or more carboxylic acid groups, an organic reducing agent for the mixture of substantially light-insensitive organic silver salts in thermal working relationship therewith and a binder, characterized in that the mixture of substantially light-insensitive organic silver salts contains a silver salt of a monocarboxylic acid and a compound represented by formula (I).
  • the compound according to formula (I) is present in a concentration of 30 to 70 mol% in the mixture of substantially light-insensitive silver salts.
  • a suspension of particles containing a substantially light-insensitive organic silver salt may be obtained by using processes disclosed in RD 17029, EP-A 754 969, US 5,891,616 and EP-A 848 286.
  • the substantially light-insensitive organic silver salt of a monocarboxylic acid in the mixture of substantially light-insensitive silver salts of organic carboxylic acids with one or more carboxylic acid groups is a silver salt of an aliphatic carboxylic acid known as a fatty acid, 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".
  • the compound according to formula (I) is selected from the group consisting of silver glutarate, silver 2-methyl glutarate, silver 3-methyl glutarate, silver 1,1-cyclopentane diacetic acetate, silver 1,1-cyclohexane diacetate, silver 1,3-cyclohexane dicarboxylate, silver citrate, silver citramalate, silver 2-methyl-succinate, silver 1,2-cyclohexane dicarboxylate, silver 3,3-tetramethylene-glutarate, silver 1,2-cyclopentane dicarboxylate, silver malate, silver tartarate, silver tetrahydrofuran-2,3,4,5-tetracarboxylate and silver itaconate.
  • No image could be obtained with photothermographic recording materials with a mixture of a silver salt of a monocarboxylic acid and silver succinate.
  • the compound according to formula (I) is selected from the group consisting of silver glutarate, silver 2-methyl succinate, silver 2,2-dimethyl-glutarate, silver 3-methylglutarate, silver tetrahydrofuran-2,3,4,5-tetracarboxylate and silver itaconate.
  • dicarboxylic acids of which compounds according to formula (I) are silver salts are commercially available. If such dicarboxylic acids are not commercially available such compounds can be prepared according to standard synthetic techniques known to organic chemists.
  • thermosensitive element comprises a mixture of a substantially light-insensitive silver salt of a monocarboxylic acid and a compound according to formula (I), an organic reducing agent therefor in thermal working relationship therewith and a binder.
  • the element may comprise a layer system in which the ingredients may be dispersed in different layers, with the proviso that the substantially light-insensitive organic silver salts and the organic reducing agent are in thermal working relationship with one another 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 substantially light-insensitive organic silver salt particles so that reduction of the organic silver salt can take place.
  • thermosensitive element can be rendered photo-addressable by the presence of a photosensitive agent which after exposure to UV, visible or IR light is capable of catalyzing or participating in a thermographic process e.g. photosensitive silver halide in catalytic association with the mixture of substantially light-insensitive silver salts.
  • a photosensitive agent which after exposure to UV, visible or IR light is capable of catalyzing or participating in a thermographic process e.g. photosensitive silver halide in catalytic association with the mixture of substantially light-insensitive silver salts.
  • Suitable organic reducing agents for the reduction of the mixture of a substantially light-insensitive silver salt of a monocarboxylic acid and a compound according to formula (I) are organic compounds containing at least one active hydrogen atom linked to O, N or C, such as is the case with, aromatic di- and tri-hydroxy compounds.
  • the organic reducing agent is a 1,2-dihydroxybenzene derivative, such as catechol, 3-(3,4-dihydroxyphenyl) propionic acid, 1,2-dihydroxybenzoic acid, gallic acid and esters e.g. methyl gallate, ethyl gallate, propyl gallate, tannic acid, and 3,4-dihydroxy-benzoic acid esters.
  • 1,2-dihydroxybenzene derivative such as catechol, 3-(3,4-dihydroxyphenyl) propionic acid, 1,2-dihydroxybenzoic acid, gallic acid and esters e.g. methyl gallate, ethyl gallate, propyl gallate, tannic acid, and 3,4-dihydroxy-benzoic acid esters.
  • the organic reducing agent is a reducing agent described in EP-B 692 733 or EP-A 903 625.
  • the organic reducing agent is a polyphenol such as the bisphenols used in the 3M Dry SilverTM materials, a sulfonamide phenol such as used in the Kodak DacomaticTM materials or a naphthol.
  • Combinations of reducing agents may also be used that on heating become reactive partners in the reduction of the substantially light-insensitive organic silver salts.
  • the film-forming binder for the photo-addressable thermosensitive element according to the present invention may be coatable from a solvent or aqueous dispersion medium.
  • the film-forming binder for the photo-addressable thermosensitive element according to the present invention may be coatable from a solvent dispersion medium, according to 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.
  • polymers derived from ⁇ , ⁇ -ethylenically unsaturated compounds such as polyvinyl chloride, after-chlorinated polyvinyl chloride, copolymers of vinyl chloride and vinylidene chloride, copolymers of vinyl chloride and vinyl acetate, polyvinyl acetate and partially hydrolyzed polyvinyl acetate, polyvinyl acetals that are made from polyvinyl alcohol as starting material in which only a part of the repeating vinyl alcohol units may have reacted with an aldehyde, preferably polyvinyl butyral, copolymers of acrylonitrile and acrylamide, polyacrylic acid esters, polymethacrylic acid esters, polystyrene and polyethylene or mixtures thereof.
  • a particularly suitable polyvinyl butyrals containing a minor amount of vinyl alcohol units are marketed under the trade name BUTVARTM B76 and BUTVARTM B79 of Monsanto USA and provides a good adhesion to paper and properly subbed polyester supports
  • the film-forming binder for the photo-addressable thermosensitive element coatable from an aqueous dispersion medium 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 (e.g.
  • phthaloyl gelatin cellulose derivatives, such as carboxymethylcellulose, polysaccharides, such as dextran, starch ethers etc., galactomannan, polyvinyl alcohol, polyvinylpyrrolidone, acrylamide polymers, homo-or co-polymerized acrylic or methacrylic acid, latexes of water dispersible polymers, with or without hydrophilic groups, or mixtures thereof.
  • 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 thermosensitive element may comprise in addition at least one polycarboxylic acid and/or anhydride thereof in a molar percentage of at least 15 with respect to all the organic silver salt(s) present and in thermal working relationship therewith.
  • the polycarboxylic acid may be aliphatic (saturated as well as unsaturated aliphatic and also cycloaliphatic) or an aromatic polycarboxylic acid, such as ortho-phthalic acid, 3-nitro-phthalic acid, tetrachlorophthalic acid, mellitic acid, pyromellitic acid and trimellitic acid and anhydrides thereof. These acids may be substituted e.g. with alkyl, hydroxyl, nitro or halogen. They may be used in anhydride form or partially esterified on the condition that at least two free carboxylic acids remain or are available in the heat recording step.
  • thermosensitive element further contains a so-called toning agent in order to obtain a neutral black image tone in the higher densities and neutral grey in the lower densities.
  • Suitable toning agents are the phthalimides and phthalazinones within the scope of the general formulae described in US 4,082,901 and the toning agents described in US 3,074,809, 3,446,648 and 3,844,797.
  • Other particularly useful toning agents are the heterocyclic toner compounds of the benzoxazine dione or naphthoxazine dione type as disclosed in GB 1,439,478, US 3,951,660 and US 5,599,647 and pyridazone as disclosed in DE 19516349.
  • Antifoggants may be incorporated into the thermographic recording materials of the present invention in order to obtain improved shelf-life and reduced fogging.
  • thermosensitive element further contains at least one antifoggant selected from the group consisting of hexamethylene tetramine (see EP 557 859 and US 5,459,028), substituted pyridazones (see DE 195 16350), benzotriazole, substituted benzotriazoles, tetrazoles and mercaptotetrazoles.
  • at least one antifoggant selected from the group consisting of hexamethylene tetramine (see EP 557 859 and US 5,459,028), substituted pyridazones (see DE 195 16350), benzotriazole, substituted benzotriazoles, tetrazoles and mercaptotetrazoles.
  • thermosensitive element further contains hexamethylene tetramine.
  • the photosensitive silver halide used in the present invention may be employed in a range of 0.75 to 25 mol percent and, preferably, from 2 to 20 mol percent 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 photo-addressable thermosensitive element of the photothermographic recording material may contain a spectral sensitizer, optionally together with a supersensitizer, for the silver halide.
  • the silver halide may be spectrally sensitized with various known dyes including cyanine, merocyanine, styryl, hemicyanine, oxonol, hemioxonol and xanthene dyes optionally, particularly in the case of sensitization to infrared radiation, in the presence of a so-called supersensitizer.
  • Useful cyanine dyes include those having a basic nucleus, such as 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.
  • a basic nucleus such as 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.
  • Useful merocyanine dyes which are preferred include those having not only the above described basic nuclei but also acid nuclei, such as 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.
  • acid nuclei such as 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.
  • imino groups or carboxyl groups are particularly effective.
  • thermographic recording material of the present invention may contain anti-halation or acutance dyes which absorb light which has passed through the photosensitive layer, thereby preventing its reflection. Such dyes may be incorporated into the thermosensitive element or in any other layer comprising the thermographic recording material of the present invention.
  • thermosensitive element may contain other additives such as free fatty acids, surface-active agents, e.g. non-ionic antistatic agents including a fluorocarbon group as e.g. in F 3 C(CF 2 ) 6 CONH(CH 2 CH 2 O)-H, silicone oil, e.g. BAYSILONETM ⁇ l A (from BAYER AG, GERMANY), ultraviolet light absorbing compounds, white light reflecting and/or ultraviolet radiation reflecting pigments, silica, colloidal silica, fine polymeric particles [e.g. of poly(methylmethacrylate)] and/or optical brightening agents.
  • surface-active agents e.g. non-ionic antistatic agents including a fluorocarbon group as e.g. in F 3 C(CF 2 ) 6 CONH(CH 2 CH 2 O)-H
  • silicone oil e.g. BAYSILONETM ⁇ l A (from BAYER AG, GERMANY)
  • ultraviolet light absorbing compounds e.g. in BAYER AG,
  • the support for the thermographic recording material according to the present invention may be transparent or translucent and is a thin flexible carrier made of transparent resin film, e.g. made of a cellulose ester, cellulose triacetate, polypropylene, polycarbonate or polyester, e.g. polyethylene terephthalate.
  • transparent resin film e.g. made of a cellulose ester, cellulose triacetate, polypropylene, polycarbonate or polyester, e.g. polyethylene terephthalate.
  • the support may be in sheet, ribbon or web form and subbed if needs be to improve the adherence to the thereon coated thermosensitive element. Suitable pretreatments of supports are, for example, treatment with a corona discharge and/or attack by solvent(s), thereby providing a micro-roughening.
  • the support may be pigmented with a blue pigment as in so-called blue-base.
  • One or more backing layers may be provided to control physical properties such as curl and static.
  • thermosensitive element is provided with a protective layer to avoid local deformation of the thermosensitive element and to improve resistance against abrasion.
  • thermosensitive element is provided with a protective layer comprising a binder, which may be solvent-soluble, solvent-dispersible, water-soluble or water-dispersible.
  • thermosensitive element is provided with a protective layer comprising solvent-soluble polycarbonates as binders as described in EP-A 614 769.
  • thermosensitive element is provided with a protective layer comprising a water-soluble or water-dispersible binder, as coating can be performed from an aqueous composition and mixing of the protective layer with the immediate underlayer can be avoided by using a solvent-soluble or solvent-dispersible binder in the immediate underlayer.
  • the protective layer according to the present invention may be crosslinked.
  • Crosslinking can be achieved by using crosslinking agents such as described in WO 95/12495.
  • Solid or liquid lubricants or combinations thereof are suitable for improving the slip characteristics of the thermographic recording materials according to the present invention.
  • thermosensitive element is provided with a protective layer comprising a solid thermomeltable lubricant such as those described in WO 94/11199.
  • the protective layer of the thermographic recording material according to the present invention may comprise a matting agent.
  • the thermosensitive element is provided with a protective layer comprising a matting agent such as described in WO 94/11198, e.g. talc particles, and optionally protrude from the protective layer.
  • any layer of the (photo)thermographic recording materials of the present invention may proceed by any thin-film coating technique known in the art.
  • slide hopper coating is used advantageously, 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.
  • Thermographic imaging is carried out by the image-wise application of heat either in analogue fashion by direct exposure through an image of by reflection from an image, or in digital fashion pixel by pixel either by using an infra-red heat source, for example with a Nd-YAG laser or other infra-red laser, with a substantially light-insensitive thermographic material preferably containing an infra-red absorbing compound, or by direct thermal imaging with a thermal head.
  • thermal printing image signals are converted into electric pulses and then through a driver circuit selectively transferred to a thermal printhead.
  • the thermal printhead consists of microscopic heat resistor elements, which convert the electrical energy into heat via Joule effect.
  • the operating temperature of common thermal printheads is in the range of 300 to 400°C and the heating time per picture element (pixel) may be less than 1.0ms, the pressure contact of the thermal printhead with the recording material being e.g. 200-500g/cm 2 to ensure a good transfer of heat.
  • the image-wise heating of the recording material with the thermal printing heads may proceed through a contacting but removable resin sheet or web wherefrom during the heating no transfer of recording material can take place.
  • Activation of the heating elements can be power-modulated or pulse-length modulated at constant power.
  • EP-A 654 355 discloses a method for making an image by image-wise heating by means of a thermal head having energizable heating elements, wherein the activation of the heating elements is executed duty cycled pulsewise.
  • EP-A 622 217 discloses a method for making an image using a direct thermal imaging element producing improvements in continuous tone reproduction.
  • Image-wise heating of the recording material can also be carried out using an electrically resistive ribbon incorporated into the material.
  • Image- or pattern-wise heating of the recording material may also proceed by means of pixel-wise modulated ultra-sound.
  • Photothermographic recording materials may be exposed with radiation of wavelength between an X-ray wavelength and a 5 microns wavelength with the image either being obtained by pixel-wise exposure with a finely focussed 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; or by direct exposure to the aspect itself or an image therefrom with appropriate illumination e.g. with UV, visible or IR light.
  • a finely focussed 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
  • a light emitting diode for
  • 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 or a thermal head, radiative heating, microwave heating etc.
  • thermographic recording materials of 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.
  • the base may be colourless or coloured, e.g. has a blue colour.
  • Application of the present invention is envisaged in the fields of both graphics images requiring high contrast images with a very steep print density applied dot energy dependence and continuous tone images requiring a weaker print density applied dot energy dependence, such as required in the medical diagnostic field.
  • thermosensitive element
  • Solution A was prepared by mixing 1000g of deionized water, 85g (0.5 moles) of silver nitrate, 15g of 6.5% nitric acid and 2.0g of mercuric nitrate at 60°C.
  • Solution B was prepared by mixing 2000g of deionized water, 26.4g (0.2 moles) of glutaric acid and 22.7g (0.57 moles) of sodium hydroxide and 50.0g of stearic acid (0.176 moles) at 70°C and had a pH of 8.8.
  • Solution A at 60°C was added to solution B at 70°C in 10s and the resulting Mixture 01 stirred for 2 minutes and then cooled to room temperature.
  • the precipitate was then filtered off, washed and dried yielding 120g of solids consisting of silver glutarate, silver stearate, stearic acid, glutaric acid and mercuric stearate-glutarate.
  • Solution C was prepared by mixing 1000g of deionized water, 85g (0.5 moles) of silver nitrate, 15g of 6.5% nitric acid and 2.0g of mercuric nitrate at 60°C.
  • Solution D was prepared by mixing 2000g of deionized water, 8.5g (0.14 moles) of glutaric acid and 22.7g (0.57 moles) of sodium hydroxide and 79.7g of stearic acid (0.28 moles) at 70°C and had a pH of 9.0.
  • Solution C at 60°C was added to solution D at 70°C in 10s and the resulting mixture stirred for 2 minutes and then cooled to room temperature.
  • the precipitate was then filtered off, washed and dried yielding 122.5g of solids consisting of silver glutarate, silver stearate, stearic acid, glutaric acid and mercuric stearate-glutarate.
  • a mixture of 76 mol% of silver behenate and 24 mol% of silver glutarate was produced by adding 0.75M aqueous sodium hydroxide to a mixture of 0.456 mol of behenic acid and 0.144 mol of glutaric acid in 750 mL to a pH of 8.7 and a UAg of 167mV and then converting the resulting sodium salts into silver salts by adding 0.8M aqueous silver nitrate until a UAg of 425mV and pH of 6.08 was realized, whereupon the mixture of silver salts precipitated out was washed and dried producing Mixture 03. The yield was 100%.
  • a mixture of 66.7 mol% of silver behenate and 33.3 mol% of silver glutarate was produced by adding 0.75M aqueous sodium hydroxide to a mixture of 0.375 mol of behenic acid and 0.1875 mol of glutaric acid in 750 mL to a pH of 8.5 and a UAg of 207mV and then converting the resulting sodium salts into silver salts by adding 0.8M aqueous silver nitrate until a UAg of 422mV and pH of 6.7 was realized, whereupon the mixture of silver salts precipitated out was washed and dried producing Mixture 03. The yield was 100%.
  • X-ray diffraction spectra carried out on Mixtures 01 to 04 showed the presence of the silver salt of a monocarboxylic acid (i.e. silver stearate in the cases of Mixtures 01 and 02 and silver behenate in the cases of Mixtures 03 and 04 and that of silver glutarate (characterized by a 2 ⁇ peak at 8.53°) and provided no evidence for the presence of mixed salts. Furthermore, the crystallinity of the mixtures of silver stearate and silver glutarate and silver behenate and silver glutarate was fairly low.
  • An emulsion for the first layer of the photo-addressable thermosensitive elements of INVENTION EXAMPLES 1 and 2 was prepared by mixing the following ingredients and solvents in the following order: Mixture 01: silver stearate/silver glutarate/stearic acid/glutaric acid/mercuric stearate-glutarate mixture 120g Methanol 720g TRITONTM X100 4.8g behenic acid 3.6g 5-nitro-indazole 1.2g phthalic anhydride 16.8g Polyvinylpyrrolidone K30 30g Methanol 90g mercuric bromide 0.48g Methanol 20g and then pearl milling the resulting mixture at 0°C for 8 hours. The photothermographic emulsion was then coated onto a subbed polyethylene terephthalate support to a wet layer thickness of 100 ⁇ m thereby producing after drying the first layer of the photo-addressable thermosensitive element.
  • the emulsion for the second layer of the photo-addressable thermosensitive elements of INVENTION EXAMPLES 1 and 2 were prepared by mixing: INVENTION EXAMPLE 1 INVENTION EXAMPLE 2 Ethyl acetate 480g 480g Cellulose propionate 40g 40g isobutanol 160g 160g Hexamethylene tetramine - 12g FC 430, a non-ionic fluorosurfactant 1g 1g bis(2-hydroxy-3,5-dimethyl-phenyl)methane 14g 14g Pyridazone 5g 5g Hydrazino-methylene-malonic acid ester 2.5g 2.5g Phthalic acid 2.5g 2.5g then coating the mixture on the first layer of the photo-addressable thermosensitive element to a wet thickness of 100 ⁇ m and finally drying to form the second layer of the photo-addressable thermosensitive element thereby producing a photothermographic recording material.
  • the photothermographic recording materials of INVENTION EXAMPLES 1 and 2 were exposed through a wedge in a KLINSCH VACUPRINTTM apparatus fitted with a mercury lamp to UV light for 10s and then the exposed material was uniformly heated at 105°C for 15s to produce a wedge image.
  • An emulsion for the first layer of the photo-addressable thermosensitive element of the high sensitivity photothermographic recording material was prepared by adding 10g of a 52.2% by weight emulsion with respect to silver of 0.1 ⁇ m edge-length cubic silver bromide grains in which the gelatin had been removed by degradation beforehand by enzymatic degradation using the enzyme trypsin, which was obtained from MERCK.
  • the resulting emulsion was coated onto a subbed polyethylene terephthalate support to a wet thickness of 100 ⁇ m. After drying it was overcoated as described in INVENTION EXAMPLE 2 to a wet thickness of 100 ⁇ m.
  • the photothermographic recording material prepared as described above was exposed through a wedge in a KLINSCH VACUPRINTTM apparatus filled with a mercury lamp to UV light for 1s at 100 lux and then the exposed material was uniformly heated at 105°C for 15s to produce a wedge image.
  • the photo-addressable element of INVENTION EXAMPLE 4 was coated as described for the photo-addressable element of INVENTION EXAMPLE 3 except that Mixture 02 of silver stearate and silver glutarate was used instead of Mixture 01 and the resulting photothermographic recording material evaluated as described for the photothermographic recording materials of INVENTION EXAMPLES 1 and 2.
  • Solution A was prepared by mixing 1000g of deionized water, 85g (0.5 moles) of silver nitrate, 15g of 6.5% nitric acid and 2.0g of mercuric nitrate at 60°C.
  • Solution B was prepared by mixing 2000g of deionized water, 162.0g of stearic acid (0.57 moles) and 22.7g (0.57 moles) of sodium hydroxide at 70°C and had a pH of 9.0.
  • Solution A at 60°C was added to solution B at 70°C in 10s and the resulting mixture stirred for 2 minutes and then cooled to room temperature.
  • the precipitate was then filtered off, washed and dried yielding 120g of solids consisting of silver stearate, stearic acid, and mercuric stearate.
  • thermosensitive element of the high sensitivity photothermographic recording material was prepared as described in INVENTION EXAMPLE 3 except that the above-described silver stearate emulsion was used instead of the silver stearate/silver glutarate emulsion of INVENTION EXAMPLES 1 and 2.
  • the photothermographic recording material prepared as described above was exposed through a wedge in a KLINSCH VACUPRINTTM apparatus fitted with a mercury lamp to UV light for 1s at 100 lux and then the exposed material was uniformly heated at 105°C for 15s to produce a wedge image.
  • COMPARATIVE EXAMPLE 1 was repeated with silver palmitate and silver glutarate being used respectively instead of silver stearate.
  • the photothermographic recording material of COMPARATIVE EXAMPLE 2 with silver palmitate was grey and fogged after 3 days in the refrigerator.
  • the photothermographic recording material of COMPARATIVE EXAMPLE 3 with silver glutarate was difficult to prepare because the silver glutarate is formed in large crystals which are difficult to grind. Furthermore, although the fresh photothermographic recording material had a high D max and normal speed, after aging for 7 days only a very low D max of ca. 0.5 could be attained after prolonged processing (ca, 30-60s at 105°C).
  • D max was ca. 0.1 even after thermal development times at 105°C of 120s. Therefore thermal development at 105°C is not possible with these mixtures of substantially light-insensitive silver salts of carboxylic acids. This indicates that the melting point of the corresponding acids to the organic silver salts cannot explain the exceptional properties of the silver glutarate/silver stearate mixture of silver salts.
  • the photothermographic recording materials of INVENTION EXAMPLE 5 and COMPARATIVE EXAMPLES 8 and 9 were exposed through a wedge in a KLINSCH VACUPRINTTM apparatus filled with a mercury lamp to UV light for 1s at 100 lux and then the exposed material was uniformly heated at 105°C at different times to produce a wedge image.
  • thermographic recording material substantially light-insensitive thermographic recording material
  • the substantially light-insensitive thermographic recording material of INVENTION EXAMPLE 6 consisted of a layer having the following composition on a subbed polyethylene terephthalate support.
  • Mixture 01 equimolar mixture of silver glutarate and silver 3.68g/m 2 stearate K7598 6.93g/m 2 ethyl 3,4-dihydroxybenzoate 1.36g/m 2 7-(ethylcarbonato)benzo[e][1,3]oxazine-2,4-dione 1.47g/m 2 Boric acid 0.42g/m 2
  • thermographic recording material of INVENTION EXAMPLE 6 the printhead was separated from the imaging layer by a thin intermediate material contacted with a slipping layer of a separable 5 ⁇ m thick polyethylene terephthalate ribbon coated successively with a subbing layer, heat-resistant layer and the slipping layer (anti-friction layer) giving a ribbon with a total thickness of 6 ⁇ m.
  • the printer was equipped with a thin film thermal head with a resolution of 300 dpi and was operated with a line time of 19ms (the line time being the time needed for printing one line). During this line time the printhead received constant power.
  • the average printing power being the total amount of electrical input energy during one line time divided by the line time and by the surface area of the heat-generating resistors was 1.6 mJ/dot, being sufficient to obtain maximum optical density in the thermographic material of INVENTION EXAMPLE 6.

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  • Engineering & Computer Science (AREA)
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  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Heat Sensitive Colour Forming Recording (AREA)
EP01000097A 2001-03-29 2001-03-29 Thermographische Materialien und Aufzeichnungsverfahren dafür Withdrawn EP1246001A1 (de)

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EP01000097A EP1246001A1 (de) 2001-03-29 2001-03-29 Thermographische Materialien und Aufzeichnungsverfahren dafür
EP02100246A EP1258775A3 (de) 2001-03-29 2002-03-13 Photothermographische Materialien und Aufzeichnungsverfahren dafür
US10/100,932 US6686133B2 (en) 2001-03-29 2002-03-19 Photothermographic materials processable at lower temperatures and recording processes therefor

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1953592A1 (de) 2007-02-02 2008-08-06 Konica Minolta Medical & Graphic, Inc. Photothermographisches Material

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0964300A1 (de) * 1998-06-08 1999-12-15 Agfa-Gevaert N.V. Thermographisches Schwarz-Weiss-Aufzeichnungsmaterial mit verbessertem Bildton

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0964300A1 (de) * 1998-06-08 1999-12-15 Agfa-Gevaert N.V. Thermographisches Schwarz-Weiss-Aufzeichnungsmaterial mit verbessertem Bildton

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1953592A1 (de) 2007-02-02 2008-08-06 Konica Minolta Medical & Graphic, Inc. Photothermographisches Material

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