EP1422551A1 - Stabilisateurs pour emploi en matériaux thermographiques d' enregistrement sensiblement non-sensibles à la lumière - Google Patents

Stabilisateurs pour emploi en matériaux thermographiques d' enregistrement sensiblement non-sensibles à la lumière Download PDF

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Publication number
EP1422551A1
EP1422551A1 EP03104031A EP03104031A EP1422551A1 EP 1422551 A1 EP1422551 A1 EP 1422551A1 EP 03104031 A EP03104031 A EP 03104031A EP 03104031 A EP03104031 A EP 03104031A EP 1422551 A1 EP1422551 A1 EP 1422551A1
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EP
European Patent Office
Prior art keywords
group
substantially light
insensitive
optionally substituted
thermographic recording
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EP03104031A
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German (de)
English (en)
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EP1422551B1 (fr
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Ingrid AGFA-GEVAERT Geuens
Johan AGFA-GEVAERT Loccufier
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Agfa Gevaert NV
Agfa Gevaert AG
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Agfa Gevaert NV
Agfa Gevaert AG
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    • 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
    • G03C1/49836—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
    • G03C2200/00—Details
    • G03C2200/40—Mercapto compound

Definitions

  • the present invention concerns stabilizers for use in substantially light-insensitive thermographic recording materials.
  • Thermography is an image-forming process including a heating step and hence includes photothermography in which the image-forming process includes image-wise exposure and direct thermal processes in which the image-forming process includes an image-wise heating step.
  • direct thermal printing a visible image pattern is produced by image-wise heating of a recording material.
  • EP-A 0 218 385 discloses a thermally developable light-sensitive material which has at least one light-sensitive silver halide containing layer on a support and which further contains a compound represented by the general formula (I): X-(-(J) m -F) n wherein X is the residue of the development restrainer; J is a divalent linkage; F is an immobilizing group that is capable of reducing the diffusibility of the compound of formula (I) or a silver salt or silver complex thereof during thermal development; m is 0 or 1; and n is an integer of 1 to 3.
  • EP-A 0 218 385 discloses the following 2-mercapto-benzothiazole compounds:
  • EP-A 0 256 820 discloses a thermal developing light-sensitive material comprising a support and, provided thereon, photographic structural layers comprising at least one layer containing light-sensitive silver halide, said photographic structural layer comprising a compound represented (1): Formula (1) X 1 -L 1 -A wherein X 1 represents a residual group of a photographic restrainer, L 1 is a mere bonding hand or a divalent group and A is selected from the group consisting of a hydrogen atom, an amino group, a hydroxyl group, a carboxyl group or a salt thereof, a sulfo group or a salt thereof and a sulfin group or a salt thereof,and a compound represented by general formula (2): Formula (2) X 2 -L 2 -B wherein X 2 represents a residual group of a photographic restrainer, L 2 is a divalent group and B is a ballast group.
  • EP-A 0 256 820 discloses the following 2-mercapto-benzothiazo
  • EP-A 0 295 507 discloses a process for the production of colour images by the photographic dye diffusion process in which a first light-sensitive sheet material is imagewise exposed, at least one of said first light-sensitive sheet material and a second light-insensitive sheet material is moistened with an aqueous liquid and the two sheet materials are together heated to 50° to 100°C with their coated surfaces in contact and then separated, said first sheet material containing, on a layer support, at least one light-sensitive silver halide emulsion layer and at least one nondiffusible colour providing compound which is capable of being decomposed imagewise in the process of development to release a diffusible dye and said second sheet material containing a salt of a strong organic base and a weak acid, wherein said first sheet material contains a combination of compounds corresponding to the following formulae I and II: wherein R 1 denotes hydrogen, alkyl with up to 6 carbon atoms, halogen, hydroxy, alkoxy or substituents which together form a condensed benzene
  • EP-A 0 295 507 further disclosed that in the above-mentioned process the first, light-sensitive sheet material additionally contains at least one compound corresponding to one of the following formulae III or IV: wherein Q denotes the group required for completing a heterocyclic group containing a 5- or 6-membered heterocyclic ring, X denotes a carboxylic or sulphonic acid group or a residue containing a carboxylic or sulphonic acid group; and wherein R 4 denotes hydrogen, alkyl with up to 18 carbon atoms, alkoxy or halogen, R 5 denotes hydrogen or an alkyl group with up to 18 carbon atoms, R 6 denotes hydrogen or an alkyl group with up to 3 carbon atoms, and n denotes 0, 1 or 2.
  • EP-A 0 295 507 also discloses as an effective compound.
  • EP-A 0 838 722 discloses a photothermographic material comprising (a) a reducible silver source, (b) a photocatalyst, (c) a reducing agent, (d) a binder, and (e) at least one compound of the following general formula (I): X-L 1 -D wherein D is an electron donative group of atoms, with the proviso that where D is a hydrazino group which is not a part of a semicarbazido group, no oxo group is substituted to the carbon atom which is directly attached to a nitrogen atom of the hydrazine, X ia a group capable of promoting adsorption to silver halide, and L 1 is a valence bond or a linking group.
  • EP-A 0 838 722 discloses at page 15 the following 2-mercapto-benzothiazole compound under the number 24:
  • US 5,922,529 discloses a photothermographic material comprising a binder, an organic silver salt, a reducing agent for silver ion, and photosensitive silver halide grains on at least one surface of a support, wherein a photosensitive layer containing the photosensitive silver halide grains further contains a compound of the formula (I) and a compound of the formula (II), and said photosensitive layer has an absorbance of 0.15 to 1.0 at an exposure wavelength, R-S(M) n wherein R is an aliphatic hydrocarbon, aryl or heterocyclic group, M is a hydrogen atom or cation, and letter n is a number determined so as to render the molecule neutral, wherein Z 1 is a group of atoms necessary to form a 5- or 6-membered nitrogenous heterocycle, each of D and D' ia a group of atoms necessary to form an acyclic or cyclic acidic nucleus, R 1 is an alkyl group, L 1 , L 2 , L 3
  • thermo development processes themselves are significantly different in that the whole material is heated at temperatures of less than 150°C for periods of seconds (e.g. 10s) in the case of photothermographic recording materials, whereas in the case of substantially light-insensitive thermographic recording materials the materials are image-wise heated at much higher temperatures for periods of ms (e.g. 3-20 ms).
  • thermal development in substantially light-insensitive thermographic recording materials involves the liquid crystalline phases of the organic silver salts, whereas this is not the case in the thermal development step in the case of photothermographic recording materials even when using the same organic silver salts. Realization of a neutral image tone is a major problem in the case of substantially light-insensitive thermographic recording materials due to the very short heating times, whereas it is much less of a problem in photothermographic recording materials due to the much longer heating times.
  • EP-A 0 713 133 discloses a thermal imaging system consisting of (i) a donor element comprising on a support a donor layer containing a binder and a thermotransferable reducing agent capable of reducing a silver source to metallic silver and (ii) a receiving element comprising on a support a receiving layer comprising a silver source, capable of being reduced by means of heat in the presence of a reducing agent, a binder and a stabiliser selected from the group consisting of benzotriazoles, heterocyclic mercaptanes, sulphinic acids, 1,3,4-triazo-indinolines, 1,3-dinitroaryl compounds, 1,2,3-triazoles, phthalic acids and phthalic acid derivatives.
  • EP-A 0 901 040 discloses a substantially light-insensitive monosheet recording material comprising 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 said thermosensitive element further contains an unsaturated carbocyclic or heterocyclic stabilizer compound substituted with a -SA group where A is hydrogen, a counterion to compensate the negative charge of the thiolate group or a group forming a symmetrical or an asymmetrical disulfide and said recording material is capable of producing prints with a numerical gradation value defined as the quotient of the fraction (2.5 - 0.1)/(E 2.5 - E 0.1 ) greater than 2.3, where E 2.5 is the energy in Joule applied in a dot area of 87 ⁇ m x 87 ⁇ m of the imaging layer that produces an optical density value of 2.5, and E 0.1 is the energy in Joule applied in a dot area of the
  • WO 94/16361 discloses a multilayer heat-sensitive material which comprises: a color-forming layer comprising: a color-forming amount of finely divided, solid colorless noble metal or iron salt of an organic acid distributed in a carrier composition; a color-developing amount of a cyclic or aromatic organic reducing agent, which at thermal copy and printing temperatures is capable of a color-forming reaction with the noble metal or iron salt; and an image-toning agent; characterized in that (a) the carrier composition comprises a substantially water-soluble polymeric carrier and a dispersing agent for the noble metal or iron salt and (b) the material comprises a protective overcoating layer for the color-forming layer.
  • WO 94/16361 discloses that suitable antifoggants are well-known photographic anti-foggants such as mercaptobenzotriazole, chromate, oxalate, citrate, carbonate, benzotriazole (BZT), 5-methylbenzotriazole, 5,6-dimethylbenzotriazole, 5-bromobenzotriazole, 5-chlorobenzotriazole, 5-nitro-benzotriazole, 4-nitro-6-chlorobenzotriazole, 5-nitro-6-chlorobenzotriazole, 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene, benzimidazole, 2-methylbenzimidazole, 5-nitrobenzimidazole, 1-phenyl-5-mercaptotetrazole, 2-mercaptobenzimidazole, 2-mercaptobenzothiazole, 2-mercaptobenzoxazole, 2-mercaptothiazoline, 2-mercapto-4-methyl-6,6'-dimethylpyr
  • thermographic imaging element comprising a substrate having coated on at least one surface thereof a thermographic imaging system comprising at least one layer comprising light-insensitive organic silver salt; reducing agent for silver ion; binder; toner; and a dye which absorbs radiation in the wavelength range of 750-1100 nm, wherein said at least one layer comprising said light-insensitive organic silver salt forms an image density greater than about 1.0 when exposed to 0.10 - 2.0 joules/cm 2 of said radiation in 0.20 to 200 microseconds.
  • WO 96/10213 does not disclose a stabilizer against the influence of light, but mentions the optional incorporation of benzotriazole in the thermographic imaging element, but only exemplifies the incorporation of benzotriazole.
  • thermographic recording materials contain the imaging-forming components both before and after image formation and unwanted image-forming must be hindered both during storage prior to printing and in prints exposed to light on light-boxes e.g. during examination by radiologists. Furthermore, such stabilization must take place without adverse effects upon the image quality particularly the image tone. Thermographic printers are being introduced with ever higher throughputs, which require thermographic recording materials able to provide stabilization without an adverse effect on the image quality at such faster throughputs. There is therefore a need for stabilizers which fulfil these requirements.
  • thermosensitive element containing a substantially light-insensitive organic silver salt, an organic reducing agent therefor in thermal working relationship therewith, a binder and at least one 2-mercapto-benzothiazole compound represented by formula (I): wherein R 1 , R 2 , R 3 and R 4 are independently hydrogen, an optionally substituted alkyl group, an optionally substituted aryl group, an alkoxy group, an ester group, a carbamate group, a carbonato group, a SO 2 R 5 group, a -NR 6 R 7 group, a nitro group, a cyano group, an acyl group, a halogen atom, an optionally alkyl or alkoxy-substituted -SO 2 NH-phenyl group, a perfluoro-alkyl group, a -CONHR 8 group, a
  • 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.
  • the L*, a* and b* CIELAB-values are defined in ASTM Norm E179-90 in a R(45/0) geometry with evaluation according to ASTM Norm E308-90.
  • Substantially light-insensitive means 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.
  • thermosensitive element as used herein is that element which contains all the ingredients, which contribute to image formation.
  • the thermosensitive element contains one or more substantially light-insensitive organic silver salts, one or more reducing agents therefor in thermal working relationship therewith and a binder.
  • the element may comprise a layer system in which the above-mentioned ingredients may be dispersed in different layers, with the proviso that the substantially light-insensitive organic silver salts are in reactive association with the reducing agents 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 particles of substantially light-insensitive organic silver salt so that reduction to silver can occur.
  • Such materials include the possibility of one or more substantially light-insensitive organic silver salts and/or one of more organic reducing agents therefor being encapsulated in heat-responsive microcapsules, such as disclosed in EP-A 0 736 799 herein incorporated by reference.
  • a substantially light-insensitive black and white monosheet thermographic recording material of the present invention can contain at least one 2-mercapto-benzothiazole compound represented by formula (I): wherein R 1 , R 2 , R 3 and R 4 are independently hydrogen, an optionally substituted alkyl group, an optionally substituted aryl group, an alkoxy group, an ester group, a carbamate group, a carbonato group, a SO 2 R 5 group, a -NR 6 R 7 group, a nitro group, a cyano group, an acyl group, a halogen atom, an optionally alkyl or alkoxy-substituted -SO 2 NH-phenyl group, a perfluoro-alkyl group, a -CONHR 8 group, a -NHOCR 9 group, a -OCOOR 10 group or a -NHCOOR 11 group; R 5 , R 9 , R 10 and R 11 are independently hydrogen, an optionally substituted al
  • the at least one benzothiazole compound according to formula (I) is a 2-mercapto-benzothiazole compound substituted by an alkyl, an aryl, an alkoxy, a nitro, a cyano or an acyl group or a halogen atom.
  • the at least one stabilizer is
  • the at least one stabilizer is
  • the 2-mercapto-benzothiazole compounds represented by formula (I), according to the present invention can be prepared from readily available starting materials using standard organic chemistry techniques known to one skilled in the art and available in such reference books such as Houben-Weyl.
  • Suitable 2-mercapto-benzothiazole (MBT) compounds include:
  • the organic silver salts are not double organic salts containing a silver cation associated with a second cation e.g. magnesium or iron ions.
  • At least one of the organic silver salts is a substantially light-insensitive silver salt of an organic carboxylic acid.
  • At least one of the organic silver salts is a substantially light-insensitive silver salt of an aliphatic carboxylic acids 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".
  • Other silver salts of an organic carboxylic acid as described in GB-P 1,439,478, e.g. silver benzoate may likewise be used to produce a thermally developable silver image.
  • Combinations of different silver salt of an organic carboxylic acids may also be used in the present invention, as disclosed in EP-A 964 300.
  • Organic silver salts may be dispersed by standard dispersion techniques. Ball mills, bead mills, microfluidizers, ultrasonic apparatuses, rotor stator mixers etc. have been found to be useful in this regard. Mixtures of organic silver salt dispersions produced by different techniques may also be used to obtain the desired thermographic properties e.g. of coarser and more finely ground dispersions of organic silver salts.
  • the reducing agent is an organic compound 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.
  • 1,2-dihydroxybenzene derivatives 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 are preferred, with those described in EP-A 0 692 733 and EP-A 0 903 625 being particularly preferred.
  • Combinations of reducing agents may also be used that on heating become reactive partners in the reduction of the one or more substantially light-insensitive organic silver salt.
  • combinations of sterically hindered phenols with sulfonyl hydrazide reducing agents such as disclosed in US 5,464,738; trityl hydrazides and formyl-phenyl-hydrazides such as disclosed in US 5,496,695; trityl hydrazides and formyl-phenyl-hydrazides with diverse auxiliary reducing agents as disclosed in US 5,545,505, US 5,545,507 and US 5,558,983; acrylonitrile compounds as disclosed in US 5,545,515 and US 5,635,339; and 2-substituted malonodialdehyde compounds as disclosed in US 5,654,130.
  • thermosensitive element Binder of the thermosensitive element
  • the film-forming binder of the thermosensitive element may be all kinds of natural, modified natural or synthetic resins or mixtures of such resins, in which the at least one organic silver salt can be dispersed homogeneously either in aqueous or solvent media: e.g.
  • cellulose derivatives starch ethers, galactomannan, 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 alcohol, 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, polyacrylates, polymethacrylates, polystyrene and polyethylene or mixtures thereof.
  • aldehyde preferably polyvinyl butyral
  • copolymers of acrylonitrile and acrylamide copolymers of acrylonitrile and
  • thermographic recording materials are: polyvinyl alcohol, polyacrylamide, polymethacrylamide, polyacrylic acid, polymethacrylic acid, polyvinylpyrrolidone, polyethyleneglycol, proteinaceous binders, polysaccharides and water-soluble cellulose derivatives.
  • a preferred water-soluble binder for use in the thermographic recording materials of the present invention is gelatine.
  • the binder to organic silver salt weight ratio is preferably in the range of 0.2 to 7, and the thickness of the thermosensitive element is preferably in the range of 5 to 50 ⁇ m. Binders are preferred which do not contain additives, such as certain antioxidants (e.g. 2,6-di-tert-butyl-4-methylphenol), or impurities which adversely affect the thermographic properties of the thermographic recording materials in which they are used.
  • additives such as certain antioxidants (e.g. 2,6-di-tert-butyl-4-methylphenol), or impurities which adversely affect the thermographic properties of the thermographic recording materials in which they are used.
  • thermosensitive element contains a toning agent, which enables a neutral black image tone to be obtained in the higher densities and neutral grey in the lower densities.
  • thermosensitive element further contains a toning agent selected from the group consisting of phthalimides, phthalazinones, benzoxazine diones and naphthoxazine diones e.g.
  • phthalimides and phthalazinones within the scope of the general formulae described in US 4,082,901; the toning agents described in US 3,074,809, 3,446,648 and 3,844,797; and 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, herein incorporated by reference.
  • the substantially light-insensitive thermographic material contains a thermosensitive element, the thermosensitive element containing one or more toning agents selected from the group consisting of phthalazinone, benzo[e][1,3]oxazine-2,4-dione, 7-methyl-benzo[e][1,3]oxazine-2,4-dione, 7-methoxy-benzo[e][1,3]oxazine-2,4-dione and 7-(ethylcarbonato)-benzo[e][1,3]oxazine-2,4-dione.
  • phthalazinone benzo[e][1,3]oxazine-2,4-dione
  • 7-methyl-benzo[e][1,3]oxazine-2,4-dione 7-methoxy-benzo[e][1,3]oxazine-2,4-dione
  • thermographic recording material further contains an auxiliary antifoggant to obtain improved shelf-life and reduced fogging.
  • the thermographic recording material further contains an antifoggant selected from the group consisting of benzotriazole, substituted benzotriazoles and aromatic polycarboxylic acid such as ortho-phthalic acid, 3-nitro-phthalic acid, tetrachlorophthalic acid, mellitic acid, pyromellitic acid and trimellitic acid and anhydrides thereof.
  • an antifoggant selected from the group consisting of benzotriazole, substituted benzotriazoles and aromatic polycarboxylic acid such as ortho-phthalic acid, 3-nitro-phthalic acid, tetrachlorophthalic acid, mellitic acid, pyromellitic acid and trimellitic acid and anhydrides thereof.
  • thermosensitive element further contains an optionally substituted benzotriazole.
  • the thermosensitive element further contains 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, may be substituted and 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.
  • the substantially light-insensitive thermographic material used in the present invention may contain one or more surfactants, which may be anionic, non-ionic or cationic surfactants and/or one or more dispersants.
  • Suitable dispersants are natural polymeric substances, synthetic polymeric substances and finely divided powders, e.g. finely divided non-metallic inorganic powders such as silica.
  • the support is transparent or translucent. It is preferably a thin flexible carrier made transparent resin film, e.g. made of a cellulose ester, e.g. 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.
  • the support may be dyed or pigmented to provide a transparent coloured background for the image.
  • the thermosensitive element is provided with a protective layer.
  • a protective layer In general this protects the thermosensitive element from atmospheric humidity and from surface damage by scratching etc. and prevents direct contact of printheads or heat sources with the recording layers.
  • Protective layers for thermosensitive elements which come into contact with and have to be transported past a heat source under pressure, have to exhibit resistance to local deformation and good slipping characteristics during transport past the heat source during heating.
  • a slipping layer being the outermost layer, may comprise a dissolved lubricating material and/or particulate material, e.g. talc particles, optionally protruding from the outermost layer. Examples of suitable lubricating materials are a surface active agent, a liquid lubricant, a solid lubricant or mixtures thereof, with or without a polymeric binder.
  • any layer of the substantially light-insensitive thermographic material used in the present invention may proceed by any coating technique e.g. such as described in Modern Coating and Drying Technology, edited by Edward D. Cohen and Edgar B. Gutoff, (1992) VCH Publishers Inc., 220 East 23rd Street, Suite 909 New York, NY 10010, USA. Coating may proceed from aqueous or solvent media with overcoating of dried, partially dried or undried layers.
  • Thermographic imaging is carried out by the image-wise application of heat either in analogue fashion by direct exposure through an image or 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. 200-1000g/linear cm, i.e. with a contact zone (nip) of 200 to 300 ⁇ m a pressure of 5000 to 50,000 g/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 ultrasound.
  • Thermographic imaging can be used for the production of reflection type prints and transparencies, in particular for use in the medical diagnostic field in which black-imaged transparencies are widely used in inspection techniques operating with a light box.
  • Subbing layer Nr. 01 has the composition: copolymer of 88% vinylidene chloride, 10% methyl acrylate and 2% itaconic acid 79.1 mg/m 2 Kieselsol® 100F, a colloidal silica from BAYER 18.6 mg/m 2 Mersolat® H, a surfactant from BAYER 0.4 mg/m 2 Ultravon® W, a surfactant from CIBA-GEIGY 1.9 mg/m 2 Subbing layer Nr.
  • 02 has the composition: copolymer of 88% vinylidene chloride, 10% methyl acrylate and 2% itaconic acid 151 mg/m 2 Kieselsol® 100F, a colloidal silica from BAYER 35 mg/m 2 Mersolat® H, a surfactant from BAYER 0.75 mg/m 2
  • thermosensitive element Ingredients in the thermosensitive element in addition to the above-mentioned ingredients:
  • thermographic materials of COMPARATIVE EXAMPLES 1 and 2 and INVENTION EXAMPLE 1 and 2 were prepared by coating a dispersion with the following ingredients in 2-butanone onto a 175 ⁇ m thick blue-pigmented polyethylene terephthalate support with CIELAB a*- and b*- values of -9.5 and -17.9 respectively subbed on the emulsion-coated side with subbing layer 01 giving layers after drying at 50°C for 1h in a drying cupboard with the compositions given in Table 1.
  • thermosensitive elements were then coated with an aqueous composition with the following ingredients, which was adjusted to a pH of 3.8 with 1N nitric acid, to a wet layer thickness of 85 ⁇ m and then dried at 50°C for 15 minutes to produce a protective layer PRO-L with the composition:
  • thermographic recording materials of COMPARATIVE EXAMPLES 1 and 2 and INVENTION EXAMPLE 1 and 2 were printed using a DRYSTARTM 4500 printer from AGFA-GEVAERT with a resolution of 508 dpi which had been modified to operate at a printing speed of 14 mm/s and a line-time of 3.5 ms instead of 7.1 ms and in which the 75 ⁇ m long (in the transport direction) and 50 ⁇ m wide thermal head resistors were power-modulated to produce different image densities.
  • the maximum densities of the images (D max ) measured through a visible filter with a MACBETHTM TR924 densitometer were all greater than 2.2.
  • the stainless steel light-box used was 650mm long, 600mm wide and 120mm high with an opening 610mm long and 560mm wide with a rim 10mm wide and 5mm deep round the opening, thereby forming a platform for a 5mm thick plate of white PVC 630mm long and 580mm wide, making the white PVC-plate flush with the top of the light-box and preventing light loss from the light-box other than through the white PVC-plate.
  • This light-box was fitted with 9 Planilux?
  • TLD 36W/54 fluorescent lamps 27mm in diameter mounted length-wise equidistantly from the two sides, with the lamps positioned equidistantly to one another and the sides over the whole width of the light-box and with the tops of the fluorescent tubes 30mm below the bottom of the white PVC plate and 35mm below the materials being tested.
  • the shifts in CIELAB a*- and b*-values at an optical density, D, of 1.0 and the shift in the CIELAB b*-value were determined for COMPARATIVE EXAMPLES 1 and 2 and INVENTION EXAMPLE 1 and 2 and the results are also given in Table 2.
  • the substantially light-insensitive thermographic recording materials of INVENTION EXAMPLES 1 and 2 containing the compounds MBT-1 and MBT-2 respectively, according to the present invention exhibit substantially lower shifts in CIELAB b*-values at an optical density, D, of 1.0 and in CIELAB b*-value at Dmin than that of COMPARATIVE EXAMPLE 2 containing the compound MBT-C1.
  • the substituted 2-mercapto-benzothiazoles MBT-1 and MBT-2 endow substantially light-insensitive thermographic recording materials with a substantially higher light stability than unsubstituted 2-mercapto-benzothiazole, MBT-C1. Comparative Example nr.
  • thermographic material of COMPARATIVE EXAMPLES 3 and 4 were prepared by coating a dispersion with the following ingredients in 2-butanone onto the support described for COMPARATIVE EXAMPLES 1 and 2 and INVENTION EXAMPLE 1 and 2 giving layers after drying at 85°C for 3 minutes in a drying cupboard with the compositions given in Table 3. Comparative example nr.
  • thermosensitive elements were then provided with a protective layer as described for COMPARATIVE EXAMPLES 1 and 2 and INVENTION EXAMPLE 1 and 2.
  • thermographic properties of the substantially light-insensitive thermographic recording materials of COMPARATIVE EXAMPLES 3 and 4 were evaluated as described for COMPARATIVE EXAMPLES 1 and 2 and INVENTION EXAMPLE 1 and 2. The results are given in Table 4.
  • a negative CIELAB b*-value indicates a bluish tone which becomes increasingly bluer as b* becomes more negative and a positive b*-value indicates a yellowish image-tone becoming more yellow as b* becomes more positive.
  • the image tone of elements of the image with a density of 1.0 have a stronger effect than the image tone of elements with lower or higher optical density.
  • thermographic material of COMPARATIVE EXAMPLES 5 to 7 and INVENTION EXAMPLES 3 to 11 were prepared by coating a dispersion with the following ingredients in 2-butanone onto the support described for COMPARATIVE EXAMPLES 1 and 2 and INVENTION EXAMPLE 1 and 2 giving layers after drying at 85°C for 3 minutes in a drying cupboard with the compositions given in Table 6. Comparative example nr.
  • thermosensitive elements were then provided with a protective layer as described for COMPARATIVE EXAMPLES 1 and 2 and INVENTION EXAMPLE 1 and 2.
  • thermographic properties of the substantially light-insensitive thermographic recording materials of COMPARATIVE EXAMPLE 5 to 7 and INVENTION EXAMPLES 3 to 11 were evaluated as described for COMPARATIVE EXAMPLES 1 and 2 and INVENTION EXAMPLE 1 and 2. The results are given in Table 7.
EP03104031A 2002-11-14 2003-10-30 Stabilisateurs pour emploi en matériaux thermographiques d' enregistrement sensiblement non-sensibles à la lumière Expired - Fee Related EP1422551B1 (fr)

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US4201582A (en) * 1974-05-02 1980-05-06 Eastman Kodak Company Photothermographic and thermographic element, composition and process
EP0218385A2 (fr) * 1985-09-17 1987-04-15 Konica Corporation Matériau sensible à la lumière développable à la chaleur
EP0256820A2 (fr) * 1986-08-08 1988-02-24 Konica Corporation Matériau sensible à la lumière développable par la chaleur
EP0353724A1 (fr) * 1988-08-05 1990-02-07 Fuji Photo Film Co., Ltd. Matériau photosensible développable à la chaleur
JPH03238453A (ja) * 1990-02-15 1991-10-24 Fuji Photo Film Co Ltd 熱現像カラー感光材料
EP0559228A1 (fr) * 1992-03-06 1993-09-08 Minnesota Mining And Manufacturing Company Eléments photothermographiques
US5686228A (en) * 1996-07-25 1997-11-11 Imation Corp. Substituted propenitrile compounds as antifoggants for black-and-white photothermographic and thermographic elements
EP0838722A2 (fr) * 1996-10-22 1998-04-29 Fuji Photo Film Co., Ltd. Matériau photothermographique, nouveau composé de 2,3-dihydrothiazole et matériau photographique photosensible à l'halogénure d'argent
EP0897130A1 (fr) * 1997-08-11 1999-02-17 Fuji Photo Film Co., Ltd. Elément d'enregistrement thermographique
US5922529A (en) * 1996-12-26 1999-07-13 Fuji Photo Film Co., Ltd. Photothermographic material
US5958668A (en) * 1996-05-22 1999-09-28 Fuji Photo Film Co., Ltd. Recording material
US20020155401A1 (en) * 2001-01-16 2002-10-24 Tetsuo Yamaguchi Photothermographic material

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6297000B1 (en) * 1997-10-14 2001-10-02 Fuji Photo Film Co., Ltd. Thermographic recording element

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4201582A (en) * 1974-05-02 1980-05-06 Eastman Kodak Company Photothermographic and thermographic element, composition and process
EP0218385A2 (fr) * 1985-09-17 1987-04-15 Konica Corporation Matériau sensible à la lumière développable à la chaleur
EP0256820A2 (fr) * 1986-08-08 1988-02-24 Konica Corporation Matériau sensible à la lumière développable par la chaleur
EP0353724A1 (fr) * 1988-08-05 1990-02-07 Fuji Photo Film Co., Ltd. Matériau photosensible développable à la chaleur
JPH03238453A (ja) * 1990-02-15 1991-10-24 Fuji Photo Film Co Ltd 熱現像カラー感光材料
EP0559228A1 (fr) * 1992-03-06 1993-09-08 Minnesota Mining And Manufacturing Company Eléments photothermographiques
US5958668A (en) * 1996-05-22 1999-09-28 Fuji Photo Film Co., Ltd. Recording material
US5686228A (en) * 1996-07-25 1997-11-11 Imation Corp. Substituted propenitrile compounds as antifoggants for black-and-white photothermographic and thermographic elements
EP0838722A2 (fr) * 1996-10-22 1998-04-29 Fuji Photo Film Co., Ltd. Matériau photothermographique, nouveau composé de 2,3-dihydrothiazole et matériau photographique photosensible à l'halogénure d'argent
US5922529A (en) * 1996-12-26 1999-07-13 Fuji Photo Film Co., Ltd. Photothermographic material
EP0897130A1 (fr) * 1997-08-11 1999-02-17 Fuji Photo Film Co., Ltd. Elément d'enregistrement thermographique
US20020155401A1 (en) * 2001-01-16 2002-10-24 Tetsuo Yamaguchi Photothermographic material

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