EP0610608B1 - Photographisches, lichtempfindliches Silberhalogenidmaterial zur Wiedergabe von medizinischen laseraufgezeichneten Bildern und Verfahren zur Verarbeitung - Google Patents

Photographisches, lichtempfindliches Silberhalogenidmaterial zur Wiedergabe von medizinischen laseraufgezeichneten Bildern und Verfahren zur Verarbeitung Download PDF

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Publication number
EP0610608B1
EP0610608B1 EP93200382A EP93200382A EP0610608B1 EP 0610608 B1 EP0610608 B1 EP 0610608B1 EP 93200382 A EP93200382 A EP 93200382A EP 93200382 A EP93200382 A EP 93200382A EP 0610608 B1 EP0610608 B1 EP 0610608B1
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EP
European Patent Office
Prior art keywords
hardcopy
silver halide
less
silver
emulsion
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EP93200382A
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English (en)
French (fr)
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EP0610608A1 (de
Inventor
Rudi August Goedeweeck
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Agfa Gevaert NV
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Agfa Gevaert NV
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Priority to EP93200382A priority Critical patent/EP0610608B1/de
Priority to DE69304675T priority patent/DE69304675T2/de
Priority to JP6037762A priority patent/JPH06250306A/ja
Publication of EP0610608A1 publication Critical patent/EP0610608A1/de
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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
    • G03C1/005—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
    • G03C1/30—Hardeners
    • 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
    • G03C1/035—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein characterised by the crystal form or composition, e.g. mixed grain
    • 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
    • G03C1/04—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
    • G03C1/043—Polyalkylene oxides; Polyalkylene sulfides; Polyalkylene selenides; Polyalkylene tellurides
    • 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
    • G03C1/035—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein characterised by the crystal form or composition, e.g. mixed grain
    • G03C2001/03511—Bromide content
    • 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
    • G03C1/035—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein characterised by the crystal form or composition, e.g. mixed grain
    • G03C2001/03558—Iodide content
    • 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
    • G03C2200/39—Laser exposure
    • 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
    • G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
    • G03C5/16—X-ray, infrared, or ultraviolet ray processes

Definitions

  • This invention relates to a method for reproducing images on a silver halide light-sensitive material for medical X-ray diagnosis for use as a hardcopy of electronically stored images.
  • a laser images is a digital system containing a high performance digital computer. Instead of just printing the images, the incoming images can be stored temporarily in an electronic memory and the data as well as the lay-out of the images can be manipulated before actually being printed on a film.
  • This electronic memory offers the possibility to buffer the incoming data from several diagnostic modalities by means of an image network, which is a real advantage in comparison with e.g. CRT imaging wherein the hard copy is exposed image by image. In that case, while one examination is taking place, the imager is unavailable for others and as a result, each diagnostic unit requires a separate CRT imager.
  • the photographic hardcopy material used in the laser imagers, combines an excellent image quality with the appropriate physical properties, necessary for an error free filmhandling by the imager.
  • image quality the photographic material preferably has high sharpness, a good image tone of the developed silver, and the appropriate contrast values to allow a high maximum density and crisp alfanumerics.
  • the access time of the laser hardcopy material should be as short as possible.
  • Factors responsible for delayed rates at which the process proceeds may be the exposure time of the film by the laser, the transport time before exposure to the system and after exposure to an automatic processor, and the processing time, dry-to-dry, of the hardcopy material.
  • the exposure time and transport time are dependant on specific features of the laser source, the mechanical construction of the system and the dimensions of the hardcopy material
  • the processing time is especially determined by the film characteristics and the chemicals used in the processing cycle. Typical modern processors have dry-to-dry cycles of less than 60 s, more preferable less than or equal to 50 seconds.
  • Hardener free chemistry offers higher convenience with regard to ecology, manipulation and regeneration of chemicals in the automatic processor provided that the hardcopy material has the expected sensitometric results as e.g. sensitivity, gradation and maximum density within restricted processing time limits.
  • the hardening agent reduces the drying time in the automatic processor by crosslinking the gelatin chains of the photographic material, thereby reducing the water adsorption of said material. Therefore, a photographic material suited for hardener free processing should be forehardened during emulsion coating in order to allow a short dry-to-dry processing cycle.
  • EP-A-0 360 616 claims a material designed for rapid processing after exposure with a laser printer. In order to reduced drying times water absorption on the emulsion side is less than 8.5 g/m 2 .
  • As light-sensitive silver halide emulsion crystals use is made, e.g., of monodisperse octahedric silverbromoiodide with a silver iodide content of 2 %.
  • ratios of gelatin to silver halide and coating weights are disclosed in order to reduce the drying time without adversely affecting sensitometry.
  • Various types of silver halide emulsions may be used therein as well as any configuration of grains in the practice of rapid processing of materials exposed by CRT or laser imaging. More specific low coating amounts of hydrophilic colloid of less than 2.5 g/m 2 and hardening the corresponding hydrophilic colloid layers to a degree to attain a swelling rate of less than 200 % are described in EP 0 457 153.
  • a medical laser hardcopy material comprising a support and on only one side thereof at least one silver halide emulsion layer and at least one hydrophilic colloid layer, wherein said material has a hardening degree corresponding with a water absorption of less than or equal to 8 g/m 2 at the emulsion side, the said water absorption being measured as follows:
  • the method for the reproduction of a medical, electronically stored image on the silver halide light-sensitive hardcopy material disclosed hereinbefore comprises the steps of
  • the hardcopy material used in this invention is particularly useful for the reproduction of electronically stored medical images by means of a laser recorder.
  • Said hardcopy material essentially is a silver halide photographic material comprising a support and at least one silver halide emulsion layer on one side of said support.
  • Said at least one silver halide emulsion layer comprises cubic silver bromide or silver bromoiodide crystals with an amount of at most 3 mole% of iodide.
  • the silver halide emulsions have monodisperse silver bromide or silver bromoiodide crystals. A monodisperse size distribution is obtained when 95% of the grains have a size that does not deviate more than 30% from the average grain size.
  • Cubic crystals are used as they allow rapid processing. In principle the same is possible with flat tabular crystals but, due to their heterogeneous silver halide grain distribution, their gradation is too low and due to the light-reflection of the developed silver which is situated at longer wavelengths the image tone is not neutral but shifted to a reddish brown colour.
  • the silver bromide or silver bromoiodide emulsions used in accordance with this invention may be prepared by mixing the halide and silver salt solutions in partially or fully controlled conditions of temperature, concentrations, sequence of addition, and rates of addition.
  • the silver halide is preferably precipitated according to the double-jet method, in the presence of a colloid binder in a temperature controlled vessel provided with a solution inlet and stirring unit.
  • a preferred precipitation technique is the double-jet method, wherein the silver ion concentration is controlled during the precipitation and wherein the flow rate of the reacting solutions is enhanced as the precipitation proceeds, at such a rate that no renucleation appears.
  • This method offers the possiblity to get well-defined crystals having a regular cubic habit within a short precipitation time.
  • Preferred cubic silverbromide or silver bromoioidide crystals have a crystal size between 0.1 and 0.4 ⁇ m and even more preferably between 0.30 and 0.35 ⁇ m for reasons of image tone of the developed silver halide crystals. As a result a high covering power of the developed grains is obtained.
  • Colloidal binders used during the silver halide precipitation are hydrophilic binders such as the frequently used gelatin.
  • Gelatin may, however, be replaced in part or integrally by synthetic, semi-synthetic, or natural polymers.
  • Synthetic substitutes for gelatin are e.g. polyvinyl alcohol, poly-N-vinyl pyrrolidone, polyvinyl imidazole, polyvinyl pyrazole, polyacrylamide, polyacrylic acid, and derivatives thereof, in particular copolymers thereof.
  • Natural substitutes for gelatin are e.g. other proteins such as zein, albumin and casein, cellulose, saccharides, starch, and alginates.
  • the semi-synthetic substitutes for gelatin are modified natural products e.g. gelatin derivatives obtained by conversion of gelatin with alkylating or acylating agents, by grafting of polymerizable monomers on gelatin or prehardened gelatins with blocked functional groups as a consequence of this prehardening treatment, and cellulose derivatives such as hydroxyalkyl cellulose, carboxymethyl cellulose, phthaloyl cellulose, and cellulose sulphates.
  • modified natural products e.g. gelatin derivatives obtained by conversion of gelatin with alkylating or acylating agents, by grafting of polymerizable monomers on gelatin or prehardened gelatins with blocked functional groups as a consequence of this prehardening treatment
  • cellulose derivatives such as hydroxyalkyl cellulose, carboxymethyl cellulose, phthaloyl cellulose, and cellulose sulphates.
  • the binder should of course dispose of an acceptably high number of functional groups, which by reaction with an appropriate hardening agent can provide a sufficiently resistant layer.
  • functional groups are especially the amino groups, but also carboxylic groups, hydroxy groups, and active methylene groups.
  • Another substitute for gelatin may be silica as has been described in EP-Applications 392 092, 517 961 and EP 91202082.3 filed August 15,1991 (corresponding to EP-A-0 528 476, published 24.2.93).
  • gelatin may be lime-treated or acid-treated.
  • the preparation of such gelatin types has been described in e.g. "The Science and Technology of Gelatin", edited by A.G. Ward and A. Courts, Academic Press 1977, page 295 and next pages.
  • the gelatin may also be an enzyme-treated gelatin as described in Bull. Soc. Sci. Phot. Japan, N° 16, page 30 (1966).
  • use is made of photographically inert gelatin so as to add a reproducible amount of chemical sensitizers at the end of the precipitation or after flocculation or washing or redispersing the silver halide emulsion.
  • flocculating agents as e.g.
  • polystyrene sulphonic acid etc. may be added before or after acidifying the emulsion.
  • Other possibilities are offered by filtration techniques e.g. dialysis, ultrafiltration etc. so that the emulsion may be washed to a desired pAg value without the requirement to be redispersed afterwards.
  • Emulsion flocculates need to be washed out by the addition of well-determined amounts of demineralized water, whether or not doped with small amounts of water-soluble salts.
  • the light-sensitive silver halide emulsion is preferably chemically sensitized as to reach its required sensitivity as described i.a. in "Chimie et Physique Photographique” by P. Glafkides, in “Photographic Emulsion Chemistry” by G.F. Duffin, in “Making and Coating Photographic Emulsion” by V.L. Zelikman et al, and in "Die Grundlagen der Photographischen mit Silberhalogeniden” edited by H. Frieser and published by Akademische Verlagsgesellschaft (1968).
  • chemical sensitization may be carried out by effecting the ripening in the presence of small amounts of compounds containing sulphur e.g.
  • the emulsions may be sensitized also by means of gold-sulphur ripeners or by means of reductors e.g. tin compounds as described in GB-A 789,823, amines, hydrazine derivatives, formamidine-sulphinic acids, and silane compounds.
  • reductors e.g. tin compounds as described in GB-A 789,823, amines, hydrazine derivatives, formamidine-sulphinic acids, and silane compounds.
  • Chemical sensitization may also be performed with small amounts of Ir, Rh, Ru, Pb, Cd, Hg, Tl, Pd, Pt, or Au.
  • One of these chemical sensitization methods or a combination thereof may be used.
  • the silver halide crystals are predigested with weakly oxidizing compounds as e.g. thiosulphonic acids before being chemically ripened.
  • weakly oxidizing compounds as e.g. thiosulphonic acids
  • Chemical sensitization may occur in the presence of spectral sensitizers.
  • the said spectral sensitizers have been chosen as a function of the laser source, showing a high light absorption at the exposure wavelength of the said laser source.
  • Spectral sensitizers may be added partially before, partially after or integrally after chemical sensitization with a total amount needed to reach the optimal coverage degree.
  • the light-sensitive silver halide emulsions may be spectrally sensitized with methine dyes such as those described by F.M. Hamer in "The Cyanine Dyes and Related Compounds", 1964, John Wiley & Sons.
  • Dyes that may be used for the purpose of spectral sensitization include cyanine dyes, merocyanine dyes, complex cyanine dyes, complex merocyanine dyes, holopolar cyanine dyes, hemicyanine dyes, styryl dyes and hemioxonol dyes.
  • Particularly valuable dyes are those belonging to the cyanine dyes, merocyanine dyes, complex merocyanine dyes, rhodacyanine dyes.
  • rhodacyanine dyes are preferred with chemical structures as described e.g. in EP-Application 473 209.
  • Suitable supersensitizers are i.a. heterocyclic mercapto compounds containing at least one electronegative substituent as described e.g. in US-A 3,457,078, nitrogen-containing heterocyclic ring-substituted aminostilbene compounds as described e.g. in US-A 2,933,390 and US-A 3,635,721, aromatic organic acid/formaldehyde condensation products as described e.g. in US-A 3,743,510, cadmium salts, and azaindene compounds.
  • the silver halide emulsion for use in accordance with the present invention may comprise compounds preventing the formation of fog or stabilizing the photographic characteristics during the production or storage of photographic elements or during the photographic treatment thereof.
  • Many known compounds may be added as fog-inhibiting agent or stabilizer to the silver halide emulsion. Suitable examples are i.a.
  • heterocyclic nitrogen-containing compounds such as benzothiazolium salts, nitroimidazoles, nitrobenzimidazoles, chlorobenzimidazoles, bromobenzimidazoles, mercaptothiazoles, mercaptobenzothiazoles , mercaptobenzimidazoles, mercaptothiadiazoles, aminotriazoles, benzotriazoles (preferably 5-methyl-benzotriazole), nitrobenzotriazoles, mercaptotetrazoles, in particular 1-phenyl-5-mercapto-tetrazole, mercaptopyrimidines, mercaptotriazines, benzothiazoline-2-thione, oxazoline-thione, triazaindenes, tetrazaindenes and pentazaindenes, especially those described by Birr in Z.
  • benzothiazolium salts such as benzothiazolium salts, nitroimidazoles, nitrobenzimidazoles,
  • Preferred stabilizers added to the emulsion in accordance with this invention are e.g. 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene, 1-phenyl-5- mercaptotetrazole etc., thioether substituted 1-phenyl-5-mercaptotetrazoles as described in EP-Spec. 53 851 being more preferable, especially if they have a solubilizable group as those described in Research Disclosure No. 24236 (1984).
  • the fog-inhibiting agents or stabilizers can be added to the silver halide emulsion prior to, during, or after the ripening thereof and mixtures of two or more of these compounds may be used.
  • a mixture of two or more silver halide emulsions having the same or different crystal sizes, a different or the same chemical ripening treatment and a different or the same coverage degree with one or more equal or different spectral sensitizers as described before may be added to at least one silver halide emulsion layer.
  • emulsion layer If more than one emulsion layer is coated onto one side of the support the same or different emulsions or emulsion mixtures may be present in the different layers. If the same emulsion or emulsion mixture is present in different emulsion layers it is a preferred embodiment to add distinct amounts of spectral sensitizer during chemical riping and/or preparation for coating so as to get a broader exposure latitude for the material according to the invention and less sensitometric fluctuations in the processing of the hardcopy material.
  • a total amount of coated silver halide crystals is preferably less than 6 g/m 2 , so as to enable the unexposed silver halide crystals to be fixed entirely in the fixation step of the rapid processing cycle.
  • the preferred homogeneous cubic crystals described hereinbefore enables the customer to reach the desired sensitometry (high gradation and high maximum density) within short processing times with such a low coating amount of silver. Besides the said crystals ensure the preferred black image tone.
  • ingredients added to the emulsion layer(s), to an antihalation undercoat layer and/or to an antistress layer and/or to one or more backing layers are antihalation dyes, developing accelerators, plasticizers, hardeners, matting agents, thickening agents, surface active agents, polymers, antistatic agents, lubricants etc.
  • Antihalation dyes are chosen as a function of the applied laser source.
  • Preferred antihalation dyes in accordance with this invention are red light absorbing dyes.
  • At least one antihalation dye is preferably added to at least one emulsion layer in amounts necessary to reduce light scattering phenomena leading to a better sharpness.
  • Preferably antihalation dyes are added in variable amounts during coating so as to adjust the sensitivity of the material. So it may be advantageous to introduce the antihalation dye or dyes by means of a dosing feeder just before coating to adjust the sensitivity of the photographic material as required by the product specifications.
  • the said antihalation dye or dyes may be present in the form of solutions thereof, in the form of a gelatinous dispersion or in a solid particle state.
  • the same or different or a mixture of different developing accelerators may be added to at least one of the hydrophilic layers at the emulsion side. More preferably at least one development accelerator is added to at least one of the protective layers, preferably to the topcoat layer.
  • Development acceleration may be accomplished with the aid of various compounds, as disclosed in Research Disclosure No. 308119, December 1989, Chapter XXI, preferably polyoxyalkylene derivatives having a molecular weight of at least 400 such as those described in e.g. US-A 3,038,805 - 4,038,075 - 4,292,400.
  • Especially preferred developing accelerators are polyoxyethylenes containing recurrent thioether groups as described in DE 2 360 878.
  • the photographic element used according to the present invention may further comprise various other additives such as e.g. compounds improving the dimensional stability of the photographic element, UV-absorbers, spacing agents, hardeners, and plasticizers.
  • additives such as e.g. compounds improving the dimensional stability of the photographic element, UV-absorbers, spacing agents, hardeners, and plasticizers.
  • Plasticizers suitable for incorporation in the emulsions according to the present invention are e.g. glycol, glycerine, or the latexes of neutral film forming polymers including polyvinylacetate, acrylates and methacrylates of lower alkanols, e.g. polyethylacrylate and polybutylmethacrylate.
  • Suitable additives for improving the dimensional stability of the photographic element may be i.a. dispersions of a water-soluble or hardly soluble synthetic polymer e.g. polymers of alkyl (meth)acrylates , alkoxy(meth)acrylates , glycidyl (meth)acrylates, (meth)acrylamides , vinyl esters, acrylonitriles, olefins , and styrenes, or copolymers of the above with acrylic acids, methacrylic acids, Alpha-Beta-unsaturated dicarboxylic acids, hydroxyalkyl (meth)acrylates , sulphoalkyl (meth)acrylates , and styrene sulphonic acids.
  • a water-soluble or soluble synthetic polymer e.g. polymers of alkyl (meth)acrylates , alkoxy(meth)acrylates , glycidyl (meth)acrylates, (meth)acryl
  • Suitable UV-absorbers may be i.a. aryl-substituted benzotriazole compounds as described in US-A 3,533,794, 4-thiazolidone compounds as described in US-A 3,314,794 and 3,352,681, benzophenone compounds as described in JP-A 2784/71, cinnamic ester compounds as described in US-A 3,705,805 and 3,707,375, butadiene compounds as described in US-A 4,045,229, and benzoxazole compounds as described in US-A 3,700,455.
  • the average particle size of spacing agents is comprised between 0.2 and 10 ⁇ m.
  • Spacing agents may be soluble or insoluble in alkali. Alkali-insoluble spacing agents usually remain permanently in the photographic element, whereas alkali-soluble spacing agents usually are removed therefrom in an alkaline processing bath.
  • Suitable spacing agents may be made i.a. of polymethyl methacrylate, of copolymers of acrylic acid and methyl methacrylate, and of hydroxypropylmethyl cellulose hexahydrophthalate. Other suitable spacing agents have been desribed in US-A 4,614,708.
  • Matting agents used in the material in accordance with this invention are polymethylmethacrylate and/or silicium dioxide particles with a particle size diameter from 0.01 to 5 ⁇ m that are added to protective topcoat layer and more preferably from 0.025 to 2 ⁇ m.
  • any thickening agent Prior to coating any thickening agent may be used so as to regulate the viscosity of the coating solution, provided that they do not particularly affect the photographic characteristics of the silver halide light-sensitive photographic material.
  • Preferred thickening agents include aqueous polymers such as polystyrene sulphonic acid, dextran, sulphuric acid esters, polysaccharides, polymers having a sulphonic acid group, a carboxylic acid group or a phosphoric acid group as well as colloidal silicas.
  • Polymeric thickeners well-known from the literature resulting in thickening of the coating solution may be used independently or in combination, even with colloidal silicas. Amounts may be suitably selected according to the kinds of silver halide and the kinds of layers or compounds to which these thickening agents are to be added. Patents concerning thickening agents are U.S. Patent No. 3.167.410, Belgian Patent No. 558.143 and JP OPI Nos. 53-18687 and 58-36768. Negative effects on physical stability possibly resulting from the addition of polymeric compounds can be avoided by exclusion of those compounds and restricting extra additions of colloidal silica.
  • the emulsions prepared and coated in the photographic material for use in accordance with the present invention are particularly advantageous for the formation of very thin emulsion layers, e.g. layers with a layer thickness of less than 5 ⁇ m, containing less than 5 g of gelatin, preferably about 3 g/m 2 .
  • Such thin coated layers offer the advantage that besides the rapid processing applicability and the rapid drying of the wet processed material an improvement in sharpness is observed.
  • the photographic element of the present invention may further comprise various kinds of surface-active agents in the photographic emulsion layer or in at least one other hydrophilic colloid layer.
  • Suitable surface-active agents include non-ionic agents such as saponins, alkylene oxides e.g.
  • polyethylene glycol polyethylene glycol/polypropylene glycol condensation products, polyethylene glycol alkyl ethers or polyethylene glycol alkylaryl ethers, polyethylene glycol esters, polyethylene glycol sorbitan esters, polyalkylene glycol alkylamines or alkylamides, silicone-polyethylene oxide adducts, glycidol derivatives, fatty acid esters of polyhydric alcohols and alkyl esters of saccharides; anionic agents comprising an acid group such as a carboxy, sulpho, phospho, sulphuric or phosphoric ester group; ampholytic agents such as aminoacids, aminoalkyl sulphonic acids, aminoalkyl sulphates or phosphates, alkyl betaines, and amine-N-oxides; and cationic agents such as alkylamine salts, aliphatic, aromatic, or heterocyclic quaternary ammonium salts, aliphatic or heterocyclic ring
  • drying characteristics in the processor are mainly determined by the water adsorption of the hydrophylic layers of the photographic material, and since the water adsorption is directly proportional to the gelatin content of the layers and inversely proportional to the amount of hardener, added to the layer, its composition is optimized with a low gelatin content and a high hardening degree so as to attain the object of this invention to allow hardener free processing within 50 seconds dry-to-dry cycle time.
  • a total amount of gelatin of less than 3 g/m 2 per side is present.
  • Hardeners may be added to the antistress layer before or during the coating procedure.
  • the binders of the photographic element especially when the binder used is gelatin, can be hardened with appropriate hardening agents such as those of the epoxide type, those of the ethylenimine type, those of the vinylsulfone type e.g. 1-3-vinylsulphonyl-2-propanol, chromium salts e.g. chromium acetate and chromium alum, aldehydes e.g. formaldehyde, glyoxal, and glutaraldehyde, N-methylol compounds e.g.
  • dimethylolurea and methyloldimethylhydantoin dioxan derivatives e.g. 2,3-dihydroxy-dioxan, active vinyl compounds e.g. 1,3,5-triacryloyl-hexahydro-s-triazine, active halogen compounds e.g. 2,4-dichloro-6-hydroxy-s-triazine, and mucohalogenic acids e.g. mucochloric acid and mucophenoxychloric acid.
  • These hardeners can be used alone or in combination.
  • the binders can also be hardened with fast-reacting hardeners such as carbamoylpyridinium salts.
  • Preferred hardening agents in accordance with this invention are formaldehyd and phloroglucinol, added respectively to the protective layer(s) and to the emulsion layer(s).
  • a hardening degree corresponding with a water absorption of the unexposed material of less than 8 g/m 2 after immersion in demineralized water at 24°C during 10 minutes is employed.
  • Backing layers applied to the material having at least one emulsion layer at one side of the hardcopy material used in accordance with this invention essentially contain hydrophilic colloids, one or more antihalation dye(s), matting agent(s), surfactant(s), antistatic agent(s), lubricant(s) and hardening agent(s).
  • a common support of the photographic silver halide emulsion material in accordance with this invention may be a hydrophobic resin support.
  • Hydrophobic resin supports are well known to those skilled in the art and are made e.g. of polyester, polystyrene, polyvinyl chloride, polycarbonate, preference being given to polyethylene terephthalate.
  • the hydrophobic resin support may be provided with one or more subbing layers known to those skilled in the art for adhering thereto a hydrophilic colloid layer.
  • subbing layers for polyethylene terephthalate supports are described e.g. in US-P 3,397,988, 3,649,336, 4,123,278 and 4,478,907.
  • Coating of the different layers of the photographic element may occur according to any of the known techniques for applying photographic coatings.
  • modern slide hopper and especially curtain coating techniques are applied.
  • polyacrylamides which are known to increase the shear viscosity can be added to the coating composition of the emulsion layer and/or protective antistress layer.
  • Suitable polyacrylamides are copoly(acrylamide-(meth)acrylic acid) e.g. COPOLY(acrylamide-acrylic acid-sodium acrylate) (87.5:4.1:8.4) in particular the commercial products ROHAFLOC SF710 and ROHAFLOC SF 580 from ROHM.
  • polyacrylamides are preferably used in amounts of 10 to 500 ppm in the coating composition of the antistress layer and coating occurs simultaneously with the emulsion layer by curtain coating. In this way the emulsion layer thickness can be reduced and coating can occur at increased speed.
  • the said convenient imaging system in accordance with this invention is characterized by the following consecutive handling steps of the hardcopy material described hereinbefore:
  • the imaging system provides at least 4 consecutive sheets per minute of a silver halide light-sensitive hardcopy material of medical, electronically stored images.
  • a short exposure time with a laser source taking less than or equal to 10 seconds for the said film format size for the hardcopy material is necessary to reach the objectives of this invention.
  • Suitable lasers may be gas lasers or solid state lasers.
  • a suitable gas laser a helium/neon gas laser is preferred.
  • a preferred laser imager fulfilling the mentioned advantages we refer to the laser imager MATRIX LR 3300, trade name product marketed by Agfa-Gevaert.
  • a particularly suitable developer solution for use in developing the hardcopy material within the scope of this invention is a developer which comprises an amount of less than 65 g of potassium sulphite per liter so as to reduce the smell of the developer to an acceptable level.
  • a suitable fixer solution for use in fixing the hardcopy material within the scope of this invention is a fixer which comprises an amount of less than 25 g of potassium sulphite per liter without the presence of acetic acid and wherein said fixer has a pH value of at least 4.5, again so as to make the fixer solution quasi odourless.
  • the said laser imager MATRIX LR 3300 is linked with the CURIX HT 330 processing unit, on top of it, as has e.g. be realized in the laser imager processor MATRIX LR 3300P Laser Imager Processor, trade name product marketed by Agfa-Gevaert, the objectives of this invention can be fully realized.
  • CURIX 330 again is a trade name product marketed by Agfa-Gevaert.
  • a monodisperse negative working 100% silverbromide emulsion of cubic crystal structure having an average diameter of 0.35 ⁇ m was prepared by means of the double-jet technique with pAg-control. After flocculation, washing and redispersion said emulsion was chemically sensitized with optimum amounts of sulphur and gold compounds to reach the best possible fog-sensitivity relationship.
  • the emulsion was divided into three parts, called respectively part A, B and C. To each of these parts, inert gelatin was added in amounts to reach ratio values of gelatin to silver halide, the silver halide expressed as the equivalent amount of silver nitrate, of 0.4, 0.6 and 0.8 for the parts A, B and C respectively. Before coating the following ingredients were added per mole of silver halide:
  • a protective coating composition was prepared containing per liter the following ingredients in demineralized water:
  • Both the emulsion layer and the antistress layer were coated simultaneously at one side onto a substrated 175 ⁇ m thick polyethylene terephtalate support.
  • the emulsion layer was coated at a concentration of silver halide corresponding to 4.8 g of silver nitrate per m 2 , the protective layer at 1 g of gelatin/m 2 . Due to the high amount the hardening agent should be added to the coating composition of the protective topcoat layer just before coating.
  • the coated materials were exposed with a He-Ne laser as a light source in a sensitometer with an exposure time of 90 ns per pixel.
  • the processing was performed in a 90 seconds dry-to-dry cycle with conventional hardening X-ray chemicals (developer G138, trade name product of Agfa-Gevaert; fixer G 334, trade name product of Agfa-Gevaert). It is clear that it is not the normal procedure to process forehardened films in hardener containing processing solutions. In this example it has only been performed so for comparative purposes.
  • the sensitivity was determined at a density of 1; the gradation between densities 1.8 and 2.4 above fog and support density.
  • the amount of water absorption, expressed in g/m 2 was determined as follows:
  • Samples No. 1, 2 and 3 from example No. 1 were processed after exposure in a dry-to-dry processing cycle of 45 ⁇ with a one-part chemistry developer and fixer without hardening agents.
  • the composition of said developer and fixer is given hereinafter.
  • composition of the developer is composition of the developer:
  • composition of the fixer is Composition of the fixer:
  • the processing machine was the CURIX HT 330, trade name product marketed by Agfa-Gevaert, with the following time (in seconds) and temperature (in °C) characteristics: Since shorter development times in the hardener-free developer and fixer solutions described hereinbefore lead to unacceptable low gradations three additional samples (No. 10, 11 and 12, see table 2) were made having the same compositions as the samples No. 1, 2 and 3 respectively of Table 1 except that 2.5 ml of an aqueous solution of the copolymer of epichloorhydrine-monoglyceryl-thiomethylethylene oxide were added as development accelerator to the coating composition of the protective layers.
  • Table 2 shows that this development accelerator is compensating very well for the loss in gradation due to shorter development times. It is clearly illustrated in the last column of Table 2 that the samples with the lowest water absorption are drying very well in the hardener-free rapid processing cycle. Said last column contains figures that are indicative for a better drying quality as the figures are lower. A "*" -sign indicates that even in extreme drying situations it was not possible to get a good drying quality for the sample. Table 2. Sensitometric results and drying quality for materials with a different degree of hardening. Sample Development Accelerator Formaldehyd Sensitivity Gradation Drying quality No. Em.

Claims (5)

  1. Verfahren zur Reproduktion eines elektronisch gespeicherten, medizinischen Bildes auf einem medizinischen Hartkopiematerial zur Wiedergabe eines laseraufgezeichneten medizinischen Bildes,
    dadurch gekennzeichnet, daß das Hartkopiematerial einen Träger und auf einer Trägerseite wenigstens eine Silberhalogenidemulsionsschicht und wenigstens eine hydrophile Kolloidschicht enthält, wobei der Härtungsgrad des Materials einer Wasserabsorption von weniger als oder gleich 8 g/m2 auf der Emulsionsseite entspricht, die Wasserabsorption wie in dieser Patentschrift beschrieben gemessen wird und die Silberhalogenidemulsion hauptsächlich aus homogenen kubischen Silberbromid- oder Silberbromiodidkristallen mit höchstens 3 Mol-% Iodidionen besteht, wobei dieses Verfahren die folgenden Stufen umfaßt :
    - die Belichtung des Hartkopiematerials mit einer Laserquelle innerhalb einer Zeit von weniger als oder gleich 10 s für ein Schnittformat von 35,6 x 43,2 cm
    - den Transport des Hartkopiematerials zu einem automatischen Entwicklungsgerät innerhalb einer Zeit von weniger als oder gleich 5 s
    - die Trocken/Trocken-Verarbeitung des Hartkopiematerials im automatischen Entwicklungsgerät innerhalb einer Zeit von weniger als 50 s, wobei Entwickler- und Fixierlösungen ohne Härtungsmittel eingesetzt werden, und
    - das Herstellen, pro Minute, von wenigstens 4 aufeinanderfolgenden Bogen mit einem Schnittformat von 35,6 x 43,2 cm.
  2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß das Hartkopiematerial homogene kubische Silberbromid- oder silberbromioididkristalle mit einem durchschnittlichen Kristalldurchmesser zwischen 0,1 und 0,4 µm enthält.
  3. Verfahren nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß der Gesamtgelatinegehalt auf der Emulsionsseite nicht mehr als 3 g/m3 beträgt und der als die äquivalente Silbernitratmenge ausgedrückte Silbergehalt auf der Emulsionsseite weniger as 5 g/m2 beträgt.
  4. Verfahren nach irgendeinem der Ansprüche 1 bis 3, dadurch gekennzeichnet, daß das photographische Silberhalogenidmaterial in wenigstens einer hydrophilen Kolloidschicht auf der Emulsionsseite wenigstens einen Entwicklungsbeschleuniger enthält.
  5. Verfahren nach Anspruch 4, dadurch gekennzeichnet, daß der Entwicklungsbeschleuniger ein Polyoxyethylenpolymeres mit sich wiederholenden Thioethergruppen ist.
EP93200382A 1993-02-12 1993-02-12 Photographisches, lichtempfindliches Silberhalogenidmaterial zur Wiedergabe von medizinischen laseraufgezeichneten Bildern und Verfahren zur Verarbeitung Expired - Lifetime EP0610608B1 (de)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP93200382A EP0610608B1 (de) 1993-02-12 1993-02-12 Photographisches, lichtempfindliches Silberhalogenidmaterial zur Wiedergabe von medizinischen laseraufgezeichneten Bildern und Verfahren zur Verarbeitung
DE69304675T DE69304675T2 (de) 1993-02-12 1993-02-12 Photographisches, lichtempfindliches Silberhalogenidmaterial zur Wiedergabe von medizinischen laseraufgezeichneten Bildern und Verfahren zur Verarbeitung
JP6037762A JPH06250306A (ja) 1993-02-12 1994-02-10 レーザー記録医療用ハードコピー材料として使用するためのハロゲン化銀感光性写真材料及び処理方法

Applications Claiming Priority (1)

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EP93200382A EP0610608B1 (de) 1993-02-12 1993-02-12 Photographisches, lichtempfindliches Silberhalogenidmaterial zur Wiedergabe von medizinischen laseraufgezeichneten Bildern und Verfahren zur Verarbeitung

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EP0610608A1 EP0610608A1 (de) 1994-08-17
EP0610608B1 true EP0610608B1 (de) 1996-09-11

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EP0679937A3 (de) * 1994-04-14 1997-10-08 Agfa Gevaert Nv Material und Verfahren zum Herstellen von Abzügen radiologischer Bilder.
EP0794456B1 (de) 1996-03-07 2003-01-29 Agfa-Gevaert Verfahren zur Wiedergabe eines elektronisch gespeicherten medizinischen Bildes auf lichtempfindlichen photographischem Material

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0738073B2 (ja) * 1987-04-14 1995-04-26 富士写真フイルム株式会社 ハロゲン化銀写真感光材料の現像方法
CA1337675C (en) * 1988-09-12 1995-12-05 James B. Philip, Jr. Ultra rapid processed, photographic element
DE68920936T2 (de) * 1988-09-22 1995-06-22 Konishiroku Photo Ind Lichtempfindliches, photographisches, zur Schnellverarbeitung geeignetes Silberhalogenidmaterial mit reduzierter Krümmung.
JP2835638B2 (ja) * 1990-05-08 1998-12-14 富士写真フイルム株式会社 ハロゲン化銀写真感光材料

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DE69304675T2 (de) 1997-03-20

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