EP0672943A1 - Matériau pour l'enregistrement d'images à l'halogénure d'argent et procédé d'obtention d'une image selon le procédé de diffusion-transfert de sel d'argent - Google Patents
Matériau pour l'enregistrement d'images à l'halogénure d'argent et procédé d'obtention d'une image selon le procédé de diffusion-transfert de sel d'argent Download PDFInfo
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- EP0672943A1 EP0672943A1 EP95200289A EP95200289A EP0672943A1 EP 0672943 A1 EP0672943 A1 EP 0672943A1 EP 95200289 A EP95200289 A EP 95200289A EP 95200289 A EP95200289 A EP 95200289A EP 0672943 A1 EP0672943 A1 EP 0672943A1
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- Prior art keywords
- layer
- image
- silver halide
- coverage
- waterpermeable
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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
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/7614—Cover layers; Backing layers; Base or auxiliary layers characterised by means for lubricating, for rendering anti-abrasive or for preventing adhesion
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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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/42—Structural details
- G03C8/52—Bases or auxiliary layers; Substances therefor
Definitions
- the present invention relates to an imaging element having a silver halide emulsion layer and to a method for obtaining an image therewith using the silver salt diffusion transfer method.
- DTR process The principle of the silver complex diffusion transfer process (hereinafter referred to as DTR process) is well known from the description in US-P 2,352.014 and in the book “Photographic Silver Halide Diffusion Processes” by André Rott and Edith Weyde - The Focal Press - London and New York, (1972).
- the silver complex is imagewise transferred by diffusion from a silver halide emulsion layer to an image receptive layer and transformed therein into a silver image generally in the presence of physical development nuclei.
- the imagewise exposed silver halide emulsion layer is arranged so as to be in contact with or is brought into contact with the image receptive layer in the presence of a developing agent and a solvent for the silver halide, thereby to convert the unexposed silver halide into a soluble silver complex.
- the silver halide In the exposed areas of the silver halide emulsion layer, the silver halide is developed into silver which is insoluble and hence cannot diffuse.
- the unexposed areas of the silver halide emulsion layer the silver halide is converted into a soluble silver complex and is transferred to an image receptive layer wherein the silver complex forms a silver image generally in the presence of development nuclei.
- the DTR-image can be formed in the image-receiving layer of a sheet or web material which is a separate element with respect to the photographic silver halide emulsion material (a so-called two-sheet DTR element) or in the image-receiving layer of a so-called single-support-element. also called mono-sheet element, which contains at least one photographic silver halide emulsion layer integral with an image-receiving layer in water permeable relationship therewith.
- the DTR process can be utilized in a wide field such as reproduction of documents, making of printing plates, preparation of black copies, and instant photography.
- an imaging material hereinafter also called negative material, having a photosensitive silver halide emulsion layer is brought into close contact with an image-receiving material, hereinafter also called positive material having an image receptive layer in a DTR processing solution generally containing a silver-complexing agent, thereby to form a silver image in the receptive layer of the positive material.
- the silver image in these cases is required to be pure black or bluish black in color and sufficiently high in density. It is also important that the silver image be high in contrast and sharpness, excellent in image reproducibility, and preferably formed with a high transfer speed.
- EP-A 402.523 it has been described that the running characteristics of a processing liquid can be improved by setting the total amount of hydrophilic colloid on the photosensitive side of an imaging element consisting of a base-layer and an emulsion layer between 6 and 8g/m2 while keeping the swelling ratio between 3.5:1 and 5.5:1.
- EP-A 93200410.4 it has been described that the running characteristics of a processing liquid can be improved by using a imaging element, conprising a base-layer and an emulsion layer with a specified composition.
- an imaging material comprising on a support a waterpermeable base layer comprising a hydrophilic colloid, a photosensitive silver halide emulsion layer comprising a hydrophilic colloid and being in waterpermeable contact with said waterpermeable base layer and a waterpermeable top layer, that is essentially free from silver halide emulsion, comprising a hydrophilic colloid and being in waterpermeable contact with said photosensitive layer characterized in that the coverage of the hydrophilic colloids comprised in said top layer is not more than 0.4 g/m2.
- an imaging material comprising on a support a photosensitive silver halide emulsion layer comprising a hydrophilic colloid and a waterpermeable top layer, essentially free from silver halide emulsion, comprising a hydrophilic colloid and being in waterpermeable contact with said photosensitive layer characterized in that the coverage of the hydrophilic colloids comprised in said top layer is not more than 0.4 g/m2 and in that the coverage of the hydrophilic colloids comprised in said photosensitive layer is not more than 2.4 g/m2, the quality of the obtained image using the DTR-process is improved. Especially the density and the speed of transfer are improved.
- the DTR-material according to the present invention further offers the advantage that it can be used in a wide range of processing conditions without a substantial loss of image quality.
- a waterpermeable layer is such that it does not substantially inhibit or restrain the diffusion of water or of compounds contained in an aqueous solution e.g. developing agents or the complexed silver.
- Layers being in waterpermeable contact with each other are layers that are contiguous to each other or only separated from each other by (a) waterpermeable layer(s).
- the coverage of the hydrophilic colloid(s) of the waterpermeable top layer depends on the nature of the colloid(s) used and the required mechanical strength but is in the present invention not more than 0.4 g/m2.
- Essentially free from silver halide emulsion means that said top layer contains less than 0.1 g/m2 , preferably none silver halide emulsion.
- Such top layer does not inhibit or restrain the diffusion transfer of the complexed silver but acts as an anti-stress layer, as a protective layer against mechanical damage of the imaging element during handling, as a layer improving the contact between the negative and the positive materials during processing, etc..
- Such layer may be transferred at least partially to the image-receiving layer without deleterious action on the image formation.
- the photosensitive silver halide emulsion layer can be coated from any photosensitive silver halide emulsion comprising a hydrophilic colloid binder provided the coverage of hydrophilic colloid contained in said layer is not more than 2.4 g/m2, more preferably not more than 2.2 g/m2.
- the weight ratio of hydrophilic colloid binder to silver halide expressed as equivalent amount of silver nitrate to binder is preferably in the range of 3:1 to 1:3 .
- the sum of the coverage of the hydrophilic colloids contained in said top layer, that is essentially free from silver halide emulsion and the emulsion layer is not more than 2.5 g/m2, more preferred not more than 2.2 g/m2.
- the photosensitive silver halide used in the present invention may be any type of photographic silver halide emulsion material suited for use in diffusion transfer reversal processing, preference being given to silver halide emulsion layers the silver halide of which is mainly silver chloride because of its relatively easy complexing with thiosulphate ions.
- the silver halide grains can have any size or shape and may be prepared by any technique known in the art, e.g. by single-jet or double jet precipitation. Negative type or direct-positive type silver halide grains may be used. Negative and positive working type silver halide emulsions are known in the art and are described e.g. in Research Disclosure, November 1976, item 15162.
- the spectral photosensitivity of the silver halide can be adjusted by proper spectral sensitization by means of the usual mono- or polymethine dyes such as acidic or basic cyanines, hemicyanines, oxonols, hemioxonols, styryl dyes or others, also tri-or polynuclear methine dyes e.g. rhodacyanines or neocyanines.
- Such spectral sensitizers have been described by e.g. F.M. HAMER in "The Cyanine Dyes and Related Compounds" (1964) Interscience Publishers, John Wiley & Sons, New York.
- the silver halide emulsions may contain the usual stabilizers Suitable stabilizers are azaindenes, preferably tetra- or penta-azaindenes, especially those substituted with hydroxy or amino groups. Compounds of this kind have been described by BIRR in Z. Wiss. Photogr. Photophys. Photochem. 47, 2-27 (1952). Other suitable stabilizers are i.a. heterocyclic mercapto compounds e.g. phenylmercaptotetrazole, quaternary benzothiazole derivatives and benzotriazole.
- the silver halide emulsions may further contain either or not in combination with one or more developing agents pH controlling ingredients, and other ingredients such as antifogging agents, development accelerators, wetting agents, and hardening agents for gelatin.
- the silver halide emulsion layer may comprise light-screening dyes that absorb scattering light and thus promote the image sharpness and, as a consequence thereof, the sharpness of the final printed copy.
- Light-absorbing dyes that can be used as light-screening dyes have been described in i.a. US-P 4,092,168, 4,311,787, DE-A 2,453,217 and GB-A 1,907,440. More details about the composition, preparation and coating of silver halide emulsions can be found in e.g. Product Licensing Index, Vol. 92, December 1971, publication 9232, p. 107-109.
- the imaging element of the present embodiment may contain other additional layers comprising a hydrophilic colloid in waterpermeable relationship with the silver halide emulsion layer.
- the total sum of the coverage of the hydrophilic colloids comprised in the photosensitive layer and in all other layers of the imaging material comprising a hydrophilic colloid and being in waterpermeable contact with the photosensitive layer is not more than 6.3 g/m2, more preferably not more than 5.6 g/m2.
- the base-layer between the support and the photosensitive silver halide emulsion layer.
- the sum of the coverage of the hydrophilic colloids contained in said base layer, the top layer, that is essentially free from silver halide emulsion and and the emulsion layer is not more than 6 g/m2, more preferably not more than 5.5 g/m2.
- said base-layer serves as an antihalation layer so that the reflectance of the support containing said antihalation layer is not more than 25% and preferably not more than 15%.
- This layer can therefore contain the same light-absorbing dyes as described above for the emulsion layer; as alternative finely divided carbon black can be used for the same antihalation purposes as described in US-P 2,327,828.
- the support it self may be selected such that it can serve as antihalation means as described in e.g. US-P 4,165,237.
- light reflecting pigments e.g. titaniumdioxide can be present.
- this layer can contain hardening agents, matting agents, e.g. silica particles, and wetting agents.
- these matting agents and/or light reflection pigments may also be present in the silver halide emulsion layer the most part however preferably being present in said base-layer.
- the light reflecting pigments may be present in a separate layer provided between the antihalation layer and the photosensitive silver halide emulsion layer.
- the hydrophilic colloid binder which is comprised in the various layers of the imaging material, is usually gelatin. But instead of or together with gelatin, use can be made of one or more other natural and/or synthetic hydrophilic colloids, e.g. albumin, casein, zein, polyvinyl alcohol, alginic acids or salts thereof, cellulose derivatives such as carboxymethyl cellulose, modified gelatin, e.g. phthaloyl gelatin etc..
- the nature of the binder is such that the amount of liquid taken up by the imaging element when soaked for 1 min. in a 0.1 N aqueous solution of NaOH is preferably between 3.5 ml and 7 ml for 1 g binder.
- the support for the imaging element may be any opaque or transparent support.
- Transparent supports are made e.g. of cellulose triacetate, polyvinyl chloride, polycarbonates, polystyrene or polyesters such as polyethylene terephthalate being provide with a suitable subbing layer(s) for adhering thereto a hydrophilic colloid layer.
- Opaque paper supports are usually made of paper coated with a water-impermeable layer of a polyolefine such as polyethylene.
- a backing layer is provided at the non-light sensitive side of the support.
- This layer which can serve as anti-curl layer can contain i.a. matting agents e.g. silica particles, lubricants, antistatic agents, light absorbing dyes, opacifying agents, e.g. titanium oxide and the usual ingredients like hardeners and wetting agents.
- the backing layer can consist of one single layer or a double layer pack.
- the imaging material can be used in conjunction with any type of image-receiving material suited for use in diffusion transfer reversal processing, said image-receiving material comprising on at least one side of the support an image receiving layer containing physical development nuclei.
- the support of the image-receiving material may be opaque or transparent, e.g. a paper support or resin support.
- Suitable physical development nuclei for use in accordance with the present invention are those commonly employed in the DTR-process e.g. noble metal nuclei of e.g. silver, palladium, gold, platinum and sulphides, selenides or tellurides of heavy metals e.g. PdS, Ag2S, AgNiS, CoS etc.. Preferably used are Ag2S or AgNiS nuclei.
- the image receiving layer comprises for best imaging results the physical development nuclei in the presence of a protective hydrophilic colloid, e.g. gelatin and/or colloidal silica, polyvinyl alcohol etc.
- a protective hydrophilic colloid e.g. gelatin and/or colloidal silica, polyvinyl alcohol etc.
- the coverage of said nuclei is preferably in the range of 0.1 mg/m2 to 10 mg/m2, and the coverage of binder is preferably in the range of 0.4 to 1.5 g/m2.
- the image-receiving element may contain in operative contact with the development nuclei thioether compounds, e.g. those described in DE-P 1,124,354, in US-P 4,013,471 and 4,072,526, and in EP-A 026,520.
- DTR-positive materials now available on the market comprises two or even three layers on the side of the support that contains an image receiving layer .
- Such materials normally contain on top of a nuclei containing layer a layer which itself preferably contains no nuclei and mainly serves to ensure good contact between the negative and positive material during transfer.
- a matting agent as is disclosed in e.g. EP-A 584407.
- the transfer behaviour of the complexed silver largely depends on the thickness of the image-receiving layer and upperlying layers and on the kind of binding agent or the mixture of binding agents used in said layers.
- the reduction of the silver salts diffusing into the image receiving layer must take place rapidly before lateral diffusion becomes substantial.
- the sum of the coverage of the hydrophilic colloids contained in said image receiving layer and said top layer is preferably less than 2 g/m2 and most preferably not more than 1.8 g/m2 and the coverage of the hydrophilic colloids contained in said top layer is preferably less than 0.45 g/m2.
- the sum of the coverage of the hydrophilic colloids contained in the top layers of the image-receiving element and the imaging element is preferably not more than 0.80 g/m2.
- the nuclei containing layer is present on a nuclei-free waterpermeable underlying undercoat layer or undercoat layer system comprising a hydrophilic colloid and having preferably a coverage in the range of 0.05 to 1 g/m2 of hydrophilic colloid
- the undercoat optionally incorporates substances that improve the image quality, e.g. incorporates a substance improving the image-tone or the whiteness of the image background.
- the undercoat may contain a fluorescent substance, silver complexing agent(s) and/or development inhibitor releasing compounds known for improving image sharpness.
- the image-receiving layer is applied on an undercoat playing the role of a timing layer in association with an acidic layer serving for the neutralization of alkali of the image-receiving layer.
- a timing layer By the timing layer the time before neutralization occurs is established, at least in part, by the time it takes for the alkaline processing composition to penetrate through the timing layer.
- Materials suitable for neutralizing layers and timing layers are disclosed in Research Disclosure July 1974, item 12331 and July 1975, item 13525.
- gelatin is used preferably as hydrophilic colloid.
- gelatin is present preferably for at least 60 % by weight and is optionally used in conjunction with an other hydrophilic colloid, e.g. polyvinyl alcohol, cellulose derivatives, preferably carboxymethyl cellulose, dextran, gallactomannans, alginic acid derivatives, e.g. alginic acid sodium salt and/or watersoluble polyacrylamides.
- Said other hydrophilic colloid may be used also in the top layer for at most 10 % by weight and in the undercoat in an amount lower than the gelatin content.
- the image-receiving layer and/or a hydrophilic colloid layer in water-permeable relationship therewith may comprise a silver halide developing agent and/or silver halide solvent, e.g. sodium thiosulphate in an amount of approximately 0.1 g to approximately 4 g per m2.
- a silver halide developing agent and/or silver halide solvent e.g. sodium thiosulphate in an amount of approximately 0.1 g to approximately 4 g per m2.
- the image-receiving layer or a hydrophilic colloid layer in water-permeable relationship therewith may comprise colloidal silica.
- At least one of the layers of the present image-receiving material substances can be contained, which play a role in the determination of the colour tone of the diffusion transfer silver image.
- Substances providing a neutral colour tone are called black-toning agents, e.g. as described in GB A 561,875 and BE A 502,525.
- the processing liquid that will be described in detail below and/or the image-receiving material contains at least one image toning agent.
- the image toning agent(s) may gradually transfer by diffusion from said image-receiving element into the processing liquid and keep therein the concentration of said agents almost steady.
- concentration of said agents almost steady.
- such can be realized by using the silver image toning agents in a coverage in the range from 1 mg/m2 to 20 mg/m2 in a hydrophilic waterpermeable colloid layer.
- Still further toning agents suitable for use in accordance with the preferred embodiment of the present invention are the toning agents described in EP-A 218752, 208346, 218753, 546599 and US-P 4.683189.
- the development nuclei containing layer and/or hydrophilic colloid layer in waterpermeable relationship therewith or a back layer at the side of the support opposite to that carrying the image receiving layer contains at least part of the silver image toning agents.
- Such procedure results actually in automatic replenishment of toning agent in the processing liquid.
- an optical brightening agent in the present image-receiving material preference is given to an optical brightening agent that is inherently by its structure resistant to diffusion or is made resistant to diffusion by use in conjunction with another substance wherein it is dissolved or whereto it is adsorbed.
- the hydrophilic colloid comprising layers of the present image-receiving material and imaging material may have been hardened to achieve enhanced mechanical strength.
- Appropriate hardening agents for hardening the natural and/or synthetic hydrophilic colloid binding agents in the image-receiving layer include e.g. formaldehyde, glyoxal, mucochloric acid, and chrome alum.
- Hardening can also be effected by incorporating a hardener precursor in said layers, the hardening of the hydrophilic colloid therein being triggered by the treatment with the alkaline processing liquid.
- Other suitable hardening agents for hardening the hydrophilic colloid binding agents in the image-receiving layer are vinylsulphonyl hardeners, e.g. as described in Research Disclosure 22,507 of Jan. 1983.
- the silver complex diffusion transfer reversal processing is by nature a wet processing including development of the exposed silver halide in the emulsion layer of the photosensitive element, the complexing of residual undeveloped silver halide and the diffusion transfer of the silver complexes into the image-receiving material wherein physical development takes place.
- the processing proceeds in alkaline aqueous medium.
- the developing agent or a mixture of developing agents can be incorporated into the alkaline processing solution and/or into the imaging material.
- the developing agent(s) can be present in the silver halide emulsion layer or is (are) preferably present in a hydrophilic colloid layer in water-permeable relationship therewith, e.g. in the anti-halation layer adjacent to the silver halide emulsion layer of the photosensitive element.
- the processing solution is merely an aqueous alkaline solution that initiates and activates the development.
- Suitable developing agents for the exposed silver halide are e.g. hydroquinone-type and 1-phenyl-3-pyrazolidone-type developing agents as well as p-monomethylaminophenol.
- a hydroquinone-type and 1-phenyl-3-pyrazolidone-type developing agent whereby the latter is preferably incorporated in one of the layers comprised on the support of the imaging material.
- a preferred class of 1-phenyl-3-pyrazolidone-type developing agents is disclosed in EP-A 498968.
- the silver halide solvent preferably sodium or ammonium thiosulphate, may be supplied from the non-light-sensitive image-receiving element as mentioned above, but it is normally at least partly already present in the alkaline processing solution.
- the amount of silver halide solvent is in the range of e.g. 10 g/l to 50 g/l.
- Preferred alkaline substances are inorganic alkali e.g. sodium hydroxide, sodium or potassium carbonate, sodium phosphate, sodium borate or alkanolamines or mixtures thereof.
- Preferably used alkanolamines are tertiary alkanolamines e.g. those described in EP-A 397925, 397926, 397927, 398435 and US-P 4,632,896.
- a combination of alkanolamines having both a pK a above or below 9 or a combination of alkanolamines whereof at least one has a pK a above 9 and another having a pK a of 9 or less may also be used as disclosed in the Japanese patent applications laid open to the public numbers 73949/61, 73953/61, 169841/61, 212670/60, 73950/61, 73952/61, 102644/61, 226647/63, 229453/63, US-P 4,362,811, 4,568,634 etc..
- the concentration of these alkanolamines is preferably from 0.1 mol/l to 0.9 mol/l.
- the alkaline processing solution usually contains preserving agents e.g. sodium sulphite, thickening agents e.g. hydroxyethylcellulose and carboxymethylcellulose, fog-inhibiting agents such as potassium bromide, black-toning agents especially heterocyclic mercapto compounds, detergents e.g. acetylenic detergents such as SURFYNOL 104, SURFYNOL 465, SURFYNOL 440 etc. all available from Air Reduction Chemical Company, New York, USA.
- preserving agents e.g. sodium sulphite
- thickening agents e.g. hydroxyethylcellulose and carboxymethylcellulose
- fog-inhibiting agents such as potassium bromide
- black-toning agents especially heterocyclic mercapto compounds
- detergents e.g. acetylenic detergents such as SURFYNOL 104, SURFYNOL 465, SURFYNOL 440 etc. all available from Air
- the DTR-process is normally carried out at a temperature in the range of 10°C to 35°C.
- the pH of the processing solution is preferably in the range of 9 to 14, more preferably in the range of 10 to 13.
- the image receiving elements according to the present invention are particularly suited for the reproduction of documents or the preparation of black copies. They can be used likewise for the reproduction of line and screen images and for the production of identification documents according to the DTR-process as described in EP-A 584407.
- a paper support having a weigth of 110 g/m2 being coated at both sides with a polyethylene layer and provided at one side with a pack of two backing layers was coated at the other side with an antihalation layer containing carbon black in such an amount that the optical density for visual light corresponded to 0.6 and gelatin in an amount of 3.9 g/m2 and wherein also hydroquinone and 1-phenyl-4-methyl-pyrazolidin-3-one were present in a coverage of 0.57 g/m2 and 0.32 g/m2.
- an orthochromatically sensitized negative working gelatino silver halide emulsion layer was coated containing an amount of silver chlorobromide (1.8 mol % bromide) equivalent to 2.0 g/m2 of silver nitrate and an amount of gelatin of 2.66 g/m2.
- the average grain size of the silver chlorobromide was 0.3 ⁇ m.
- the silver halide emulsion layer was overcoated with a thin protective gelatin layer at a coverage of 0.5 g/m2.
- the layer nearest to the support of the backing layer pack contained 4 g/m2 of gelatin, 1.5 g/m2 of a colloidal silica and 0.021 g/m2 of wetting agent F15C7-COONH4.
- the second backing layer contained 0.3 g/m2 of gelatin, 0.5 g/m2 of the antistatic agent co(tetraallyloxyethane / methacrylate / acrylic acid-K-salt) polymer and 0.05 g/m2 of hardening agent triacrylformal.
- Imaging material N2 was prepared similar to imaging material N1 with the exception that the gelatine coverage in the top layer was 0.4 g/m2.
- Imaging material N3 was prepared similar to imaging material N1 with the exception that the gelatine coverage in the antihalation layer, the silver halide emulsion layer and the top layer were respectively 2.5 g/m2, 1.0 g/m2 and 0.4 g/m2.
- a subbed polyethylene terephthalate film support was coated at both sides at a dry coverage of 1.77 g/m2 with an image-receiving layer containing silver-nickel sulphide nuclei dispersed in gelatin. This layer was applied by slide hopper coating so that the nuclei were in an undermost coating of 1.22 g gelatin/m2 and a top layer was provided of 0.55 g gelatin/m2.
- the image-receiving material P2 was prepared similar to the image-receiving material P1 with the exception that the gelatine coverage in the image-receiving layer and the top layer were respectively 0.5 g/m2 and 0.4 g/m2.
- the photographic materials were exposed through a sensitometric wedge in a contact exposure apparatus operating with a light source having a colour temperature of 3200 °K.
- the exposed photographic materials were pre-moistened with a processing liquid, the contact time with said liquid being 6 seconds before being pressed together with an image-receiving material as defined above.
- the transfer processor employed was a COPYPROOF (registered trade name of AGFA-GEVAERT N.V.) type CP 380.
- COPYPROOF registered trade name of AGFA-GEVAERT N.V.
- the imaging elements N1 and N2 (comparative imaging materials) having a gelatine coverage in the top layer of 0.5 g/m2 respectively 0.4 g/m2 and a gelatine coverage in the emulsion layer of 2.66 g/m2 show at different contact times a lower transfer speed and give images with a lower D max than the imaging element N3 (imaging material according to the invention) having a gelatine coverage in the top layer of 0.4 g/m2 and in the emulsion layer of 1.0 g/m2 .
- Using a positive material with a thinner top layer also helps in obtaining these properties, but not to the same extent.
- a polyethyleneterephthalate film support (with a hydrophilic adhesion layer) of 0.1mm thickness and provided at one side with a pack of two backing layers was coated at the other side with an antihalation layer containing carbon black in such an amount that the optical density for visual light corresponded to 0.8 and gelatin in an amount of 4.7 g/m2.
- an orthochromatically sensitized direct-positive working gelatino silver halide emulsion layer was coated containing an amount of silver chlorobromide (1.8 mol % bromide) equivalent to 2.75 g/m2 of silver nitrate and an amount of gelatin of 3.26 g/m2.
- the average grain size of the silver chlorobromide was 0.25 ⁇ m.
- the silver halide emulsion layer was overcoated with a thin protective gelatin layer at a coverage of 0.5 g/m2.
- the backing layer nearest to the support contained 4.5 g/m2 of gelatin and 1.5 g/m2 of carbon black.
- the second backing layer contained 0.6 g/m2 of gelatin, 1 g/m2 of the antistatic agent co(tetraallyloxyethane / methacrylate / acrylic acid-K-salt) polymer and 0.1 g/m2 of hardening agent triacrylformal
- Imaging material N5 was prepared similar to imaging material N4 with the exception that the gelatine coverage in the antihalation layer, the silver halide emulsion layer and the top layer were respectively 3.0 g/m2, 2.0 g/m2 and 0.4 g/m2, Composition of the processing liquid: A3 A4 Hydroxyethylcellulose (g) 1 1 EDTA (g) 2 2 Na2SO3 (anhydrous) (g) 45 45 Na2S203 (anhydrous) (g) 14 21 Hydroquinone 13 13 1-Phenyl-4-methyl- pyrazolidin-3-one 4.7 4.7 KBr (g) 0.5 0.5 1-Phenyl-5-mercapto-tetrazole (g) 0.08 0.1 1-(3,4 dichlorophenyl)-1-H-tetrazole-5-thiol (g) 0.04 0.02 MMEA (ml) 30 0 Boric acid 0 31 Sodium hydroxide 1.9 66 Water up to 1 litre 1 litre pH 10.9 1
- the photographic materials were exposed, processed and the obtained test wedge prints in the image-receiving materials evaluated as described in example 1 with the exception that the transfers were carried out at a processing temperature of 32 °C at contact times of 15 and 30 seconds.
- the imaging element N4 (comparative imaging material) having a gelatine coverage in the top layer of 0.5 g/m2 and in the emulsion layer of 3.26 g/m2 shows at different contact times a lower transfer speed and gives images with a lower D max than the imaging element N5 (imaging material according to the invention) having a gelatine coverage in the top layer of 0.4 g/m2 and in the emulsion layer of 2.0 g/m2 .
- a positive material with a thinner top layer also helps in obtaining these properties, but not to the same extent.
- the best results are obtained with the combination of the imaging element N5 (imaging material according to the invention) with the thin-layer positive material P2. These results are obtained not only by using the processing liquid A3, containing an alkanolamine, but also by using the processing liquid A4, which is free of alkanolamines and comprises as alkaline substance sodium borate.
- a polyethyleneterephthalate film support (with a hydrophilic adhesion layer) of 0.1mm thickness and provided at one side with a pack of two backing layers was coated at the other side with an antihalation layer containing carbon black in such an amount that the optical density for visual light corresponded to 0.6 and gelatin in an amount of 3.9 g/m2.
- an orthochromatically sensitized negative working gelatino silver halide emulsion layer was coated containing an amount of silver chlorobromide (1.8 mol % bromide) equivalent to 2.5 g/m2 of silver nitrate and an amount of gelatin of 3.0 g/m2.
- the average grain size of the silver chlorobromide was 0.3 ⁇ m.
- the silver halide emulsion layer further contained hydroquinone and 1-phenyl-4-methyl-pyrazolidone at a coverage of 0.9 g and 0.25 g/m2 respectively.
- the silver halide layer was then covered with a gelatin layer containing 0.5 g/m2 of gelatin.
- the backing layer packet was identical to the backing layer packet of imaging material N1
- Imaging material N7 was prepared similar to imaging material N6 with the exception that the gelatine coverage in the antihalation layer, the silver halide emulsion layer and the top layer were respectively 3.06 g/m2, 2.14 g/m2 and 0.33 g/m2,
- Imaging material N8 was prepared similar to imaging material N1 with the exception that the gelatine coverage in the antihalation layer, the silver halide emulsion layer and the top layer were respectively 2.6 g/m2, 1.86 g/m2 and 0.35 g/m2,
- the image-receiving material P3 was prepared similar to the image-receiving material P1 with the exception that the gelatine coverage in the image-receiving layer and the top layer were respectively 1.4 g/m2 and 0.4 g/m2,
- One side of a paper support having a weight of 110 g/m2 and being coated at both sides with a polyethylene layer was coated at a dry coverage of 1.7 g/m2 with an image-receiving layer containing silver-nickel sulphide nuclei and gelatin.
- This layer was applied by slide hopper coating so that the nuclei were in an undermost coating of 1.3 g gelatin/m2 and a top layer was provided of 0.4 g of gelatin/m2.
- the photographic materials were exposed, processed and the obtained test wedge prints in the image-receiving materials evaluated as described in example 1 with the exception that the transfer contact time was 20 seconds for the paper type image receiving material P4 and 60 seconds for the resin film type image receiving materials P1 and P3 and that transfers were carried out at different processing liquid temperatures being 16, 22 and 32 °C respectively.
- the imaging element N6 (comparative imaging material) having a gelatine coverage in the top layer of 0.5 g/m2 and in the emulsion layer of 3.0 g/m2 shows at different contact times a lower transfer speed and gives images with a lower D max than the imaging element N7 (imaging material according to the invention) having a gelatine coverage in the top layer of 0.33 g/m2 and in the emulsion layer of 2.14 g/m2 .
- Using a positive material with a thinner top layer increases these effects. Particularly good results are obtained with the combination of the imaging element N7 (imaging material according to the invention) with the thin-top layer positive material P3.
- exhaustion of the processing liquid has a less detrimental effect on D max of the images, obtained from the imaging element N7 (imaging material according to the invention) than on D max of the images, obtained from the imaging element N6 (comparative imaging material) which allows a longer use of the processing liquid while still obtaining images of acceptable quality.
- imaging materials N7 and N8 are obtained by using the processing liquids A5 (a developing solution) or A6 (an activating solution) , which are free of alkanolamines and comprises as alkaline substance sodium phosphate and/or sodium carbonate.
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- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Architecture (AREA)
- Structural Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP19950200289 EP0672943B1 (fr) | 1994-03-04 | 1995-02-07 | Matériau pour l'enregistrement d'images à l'halogénure d'argent et procédé d'obtention d'une image selon le procédé de diffusion-transfert de sel d'argent |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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EP94200552 | 1994-03-04 | ||
EP94200552 | 1994-03-04 | ||
EP19950200289 EP0672943B1 (fr) | 1994-03-04 | 1995-02-07 | Matériau pour l'enregistrement d'images à l'halogénure d'argent et procédé d'obtention d'une image selon le procédé de diffusion-transfert de sel d'argent |
Publications (2)
Publication Number | Publication Date |
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EP0672943A1 true EP0672943A1 (fr) | 1995-09-20 |
EP0672943B1 EP0672943B1 (fr) | 2000-01-12 |
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Application Number | Title | Priority Date | Filing Date |
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EP19950200289 Expired - Lifetime EP0672943B1 (fr) | 1994-03-04 | 1995-02-07 | Matériau pour l'enregistrement d'images à l'halogénure d'argent et procédé d'obtention d'une image selon le procédé de diffusion-transfert de sel d'argent |
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EP (1) | EP0672943B1 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0816922A1 (fr) * | 1996-07-04 | 1998-01-07 | Agfa-Gevaert N.V. | Elément formateur d'images pour la production d'une plaque d'impression améliorée suivant le procédé diffusion-transfert de sel d'argent |
Citations (12)
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GB869190A (en) * | 1958-01-20 | 1961-05-31 | Agfa Ag | A process for the production of direct positives by the silver salt diffusion process |
US3383211A (en) * | 1963-04-26 | 1968-05-14 | Gevaert Photo Prod Nv | Lithographic printing plates |
US3396018A (en) * | 1963-05-17 | 1968-08-06 | Eastman Kodak Co | Diffusion transfer system |
US3893855A (en) * | 1973-01-29 | 1975-07-08 | Polaroid Corp | Photographic ligand for inducing disproportionation of silver {30 1 and processes of use thereof |
GB2110400A (en) * | 1981-09-21 | 1983-06-15 | Fuji Photo Film Co Ltd | Silver halide photographic light-sensitive material |
US4530898A (en) * | 1984-02-29 | 1985-07-23 | Polaroid Corporation | Photographic products and processes providing a negative image |
EP0208346A2 (fr) * | 1985-06-11 | 1987-01-14 | Agfa-Gevaert N.V. | Procédé d'inversion par diffusion-transfert |
JPS62222250A (ja) * | 1986-03-24 | 1987-09-30 | Mitsubishi Paper Mills Ltd | 銀錯塩拡散転写法 |
EP0306561A1 (fr) * | 1987-09-08 | 1989-03-15 | Agfa-Gevaert N.V. | Matériau récepteur d'image |
EP0383283A2 (fr) * | 1989-02-17 | 1990-08-22 | Konica Corporation | Matériau photographique à l'halogénure d'argent sensible à la lumière |
EP0402523A2 (fr) * | 1989-06-16 | 1990-12-19 | Mitsubishi Paper Mills, Ltd. | Produit photosensible pour procédé de transfert |
US5272046A (en) * | 1990-10-25 | 1993-12-21 | Fuji Photo Film Co., Ltd. | Processing method for a silver halide photographic material |
-
1995
- 1995-02-07 EP EP19950200289 patent/EP0672943B1/fr not_active Expired - Lifetime
Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB869190A (en) * | 1958-01-20 | 1961-05-31 | Agfa Ag | A process for the production of direct positives by the silver salt diffusion process |
US3383211A (en) * | 1963-04-26 | 1968-05-14 | Gevaert Photo Prod Nv | Lithographic printing plates |
US3396018A (en) * | 1963-05-17 | 1968-08-06 | Eastman Kodak Co | Diffusion transfer system |
US3893855A (en) * | 1973-01-29 | 1975-07-08 | Polaroid Corp | Photographic ligand for inducing disproportionation of silver {30 1 and processes of use thereof |
GB2110400A (en) * | 1981-09-21 | 1983-06-15 | Fuji Photo Film Co Ltd | Silver halide photographic light-sensitive material |
US4530898A (en) * | 1984-02-29 | 1985-07-23 | Polaroid Corporation | Photographic products and processes providing a negative image |
EP0208346A2 (fr) * | 1985-06-11 | 1987-01-14 | Agfa-Gevaert N.V. | Procédé d'inversion par diffusion-transfert |
JPS62222250A (ja) * | 1986-03-24 | 1987-09-30 | Mitsubishi Paper Mills Ltd | 銀錯塩拡散転写法 |
EP0306561A1 (fr) * | 1987-09-08 | 1989-03-15 | Agfa-Gevaert N.V. | Matériau récepteur d'image |
EP0383283A2 (fr) * | 1989-02-17 | 1990-08-22 | Konica Corporation | Matériau photographique à l'halogénure d'argent sensible à la lumière |
EP0402523A2 (fr) * | 1989-06-16 | 1990-12-19 | Mitsubishi Paper Mills, Ltd. | Produit photosensible pour procédé de transfert |
US5272046A (en) * | 1990-10-25 | 1993-12-21 | Fuji Photo Film Co., Ltd. | Processing method for a silver halide photographic material |
Non-Patent Citations (1)
Title |
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PATENT ABSTRACTS OF JAPAN vol. 12, no. 88 (P - 678)<2935> 23 March 1988 (1988-03-23) * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0816922A1 (fr) * | 1996-07-04 | 1998-01-07 | Agfa-Gevaert N.V. | Elément formateur d'images pour la production d'une plaque d'impression améliorée suivant le procédé diffusion-transfert de sel d'argent |
Also Published As
Publication number | Publication date |
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EP0672943B1 (fr) | 2000-01-12 |
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