EP0345514B1 - Matériau photographique couleur à l'halogénure d'argent - Google Patents

Matériau photographique couleur à l'halogénure d'argent Download PDF

Info

Publication number
EP0345514B1
EP0345514B1 EP89109108A EP89109108A EP0345514B1 EP 0345514 B1 EP0345514 B1 EP 0345514B1 EP 89109108 A EP89109108 A EP 89109108A EP 89109108 A EP89109108 A EP 89109108A EP 0345514 B1 EP0345514 B1 EP 0345514B1
Authority
EP
European Patent Office
Prior art keywords
alkyl
hydrogen
aryl
halogen
alkoxy
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP89109108A
Other languages
German (de)
English (en)
Other versions
EP0345514A3 (en
EP0345514A2 (fr
Inventor
Werner Dr. Liebe
Johannes Dr. Sobel
Fritz Dr. Nittel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Agfa Gevaert AG
Original Assignee
Agfa Gevaert AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Agfa Gevaert AG filed Critical Agfa Gevaert AG
Publication of EP0345514A2 publication Critical patent/EP0345514A2/fr
Publication of EP0345514A3 publication Critical patent/EP0345514A3/de
Application granted granted Critical
Publication of EP0345514B1 publication Critical patent/EP0345514B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/815—Photosensitive materials characterised by the base or auxiliary layers characterised by means for filtering or absorbing ultraviolet light, e.g. optical bleaching

Definitions

  • the invention relates to a color photographic silver halide recording material, in particular one with a reflective base, which provides higher color densities.
  • Color photographic materials are known from EP 0 243 199 A2, in particular color negative paper, which contain in at least one light-sensitive layer a silver halide with at least 80 mol% of chloride, which have a layer with a UV light-absorbing agent which is liquid at room temperature, and which are hardened with a vinyl sulfone hardener.
  • This color negative paper can be used in the so-called short-term process, in which the development time is 45 seconds, to produce color image images.
  • the material is characterized by reduced pressure desensitization, but still does not provide really satisfactory maximum densities.
  • the invention thus relates to a color photographic silver halide recording material which, on a support, preferably a reflective support, contains at least one silver halide emulsion layer, the silver halide grains of which contain at least 80 mol% of silver chloride, and at least one layer, preferably a non-light-sensitive layer, which contains an ultraviolet light absorbent, which is liquid at 15 ° C, contains and the material is hardened with an instant hardener.
  • Immediate hardeners are understood to mean compounds which crosslink suitable binders in such a way that the hardening is completed to such an extent immediately after casting, at the latest after 24 hours, preferably at the latest after 8 hours, that no further change in the sensitometry caused by the crosslinking reaction and the swelling of the layer structure occurs .
  • Swelling is understood to mean the difference between the wet film thickness and the dry film thickness during the aqueous processing of the film (Photogr. Sci. Eng. 8 (1964); 275; Photogr. Sci. Eng. (1972), 449).
  • the instant hardener is used in particular in an amount of 0.1 to 5 mmol / m2, preferably 0.5 to 1.7 mmol / m2.
  • Alkyl is especially C1-C20-alkyl optionally substituted by halogen, hydroxy, sulfo, C1-C20-alkoxy.
  • Aryl unless otherwise defined, is in particular optionally substituted by halogen, sulfo, C1-C20-alkoxy or C1-C20-alkyl C6-C14 aryl.
  • Aralkyl unless otherwise defined, is in particular substituted by halogen, C1-C20-alkoxy, sulfo or C1-C20-alkyl C7-C20-aralkyl, alkoxy, unless otherwise defined, in particular is C1-C20-alkoxy.
  • X ⁇ is preferably a halide ion such as Cl ⁇ , Br ⁇ or BF4 ⁇ , NO3 ⁇ , (SO4 2 ⁇ ) 1/2 , ClO4 ⁇ , CH3OSO3 ⁇ , PF6 ⁇ , CF3SO3 ⁇ and in particular a -SO3 ⁇ covalently linked to the hardener molecule Group, where the -SO3 ⁇ group can be directly connected to the heterocycle via a substituent (see definitions alkyl, aryl, aralkyl) or in the formulas (a), (b), (c).
  • a substituent see definitions alkyl, aryl, aralkyl
  • Alkenyl is especially C2-C20 alkenyl
  • alkylene is especially C2-C20 alkylene
  • Arylene in particular phenylene, aralkylene in particular benzylene and alkaralkylene in particular xylylene.
  • Suitable N-containing ring systems that can represent Z are shown on the previous page.
  • the pyridine ring is preferred.
  • R36 and R37 together with the nitrogen atom to which they are attached, in particular form a pyrrolidine or piperidine ring bonded by 2 oxo groups in the o- and o'-position, which may be benzo, cyclohexeno- or [2.2.1] -bicyclohexenocondensed .
  • Acyl is especially C1-C10 alkylcarbonyl or benzoyl; Carbalkoxy is especially C1-C10 alkoxycarbonyl; Carbamoyl is especially mono- or di-C1-C4 alkylaminocarbonyl; Carbaroxy is especially phenoxycarbonyl.
  • Groups R24 which can be split off by nucleophilic agents are, for example, halogen atoms, C1-C15 alkylsulfonyloxy groups, C7-C15 aralkylsulfonyloxy groups, C6-C15 arylsulfonyloxy groups and 1-pyridinyl radicals.
  • the compounds can be prepared in a simple manner known from the literature.
  • the secondary amines are e.g. with phosgene, the carbamic acid chlorides, which are then reacted with aromatic, heterocyclic nitrogen-containing compounds in the absence of light.
  • the preparation of compound 3 is described in Chemical Reports 40, (1907), page 1831. Further information on the synthesis can be found in DE-OS 2 225 230, DE-OS 2 317 677 and DE-OS 2 439 551.
  • JP-OSs 44 140/82 and 46 538/82 and JP-PS 50 669/83 Methods for the synthesis of these compounds are described in more detail in JP-OSs 44 140/82 and 46 538/82 and JP-PS 50 669/83.
  • the compounds (a) are particularly preferred.
  • the binder to be cured used in the layers which are subjected to the curing process according to the invention is a proteinaceous binder which contains free amino groups and free carboxyl groups.
  • Gelatin is a preferred example. Gelatin is mainly used in photographic recording materials as a binder for the light-sensitive substances, the coloring compounds and, if appropriate, other additives. Such recording materials often have a large number of different layers.
  • the hardening by means of an immediate hardener is usually carried out in such a way that the hardening agent is applied as the last layer to the layers to be hardened, whereby further substances, such as the UV absorbers, antistatic agents, matting agents and polymeric organic particles, can be added to the hardening coating solution.
  • the layer containing the hardening agent can be applied simultaneously with or after the casting of the remaining layers by means of cascade or curtain coaters.
  • the casting temperature can be varied over a wide range, e.g. B. between 45 and 5 ° C, preferably between 38 and 18 ° C.
  • UV absorbers which are liquid according to the invention are given below.
  • the UV absorbers that are liquid at room temperature can be used individually or as a mixture with one another.
  • UV absorbers that are liquid at room temperature with UV absorbers that are solid at room temperature, or to produce mixtures of UV absorbers that are solid at room temperature, as long as the mixture is liquid even at 15 ° C.
  • the 2- (2-hydroxyphenyl) benzotriazole compounds are known and are described, for example, in US Pat. Nos. 3,754,919, 4,220,711 and 4,518,686.
  • UV absorber it can also be advantageous to divide up the total amount of UV absorber, to use a part in the uppermost, non-light-sensitive protective layer and a part in a non-light-sensitive intermediate layer, in particular over the purple layer or in a light-sensitive layer over the purple layer.
  • the photographic material according to the invention contains in particular at least one blue-sensitive layer, to which at least one yellow coupler is assigned, at least a green-sensitive layer to which at least one magenta coupler is assigned and at least one red-sensitive layer to which at least one cyan coupler is assigned.
  • the at least one blue-sensitive layer is preferably located closest to the support and the at least one red-sensitive layer is most distant from the support.
  • the silver halides of all light-sensitive layers preferably contain at least 80 mol% of chloride, in particular 95 to 100 mol% of chloride, 0 to 5 mol% of bromide and 0 to 1 mol% of iodide.
  • the silver halide can be predominantly compact crystals, e.g. are regular cubic or octahedral or can have transitional forms.
  • platelet-shaped crystals may preferably also be present, the average ratio of diameter to thickness of which is preferably at least 5: 1, the diameter of a grain being defined as the diameter of a circle with a circle content corresponding to the projected area of the grain.
  • the layers can also have tabular silver halide crystals in which the ratio of diameter to thickness is greater than 5: 1, e.g. 12: 1 to 30: 1.
  • the silver halide grains can also have a multi-layered grain structure, in the simplest case with an inner and an outer grain area (core / shell), the halide composition and / or other modifications, such as doping the one individual grain areas are different.
  • the average grain size of the emulsions is preferably between 0.2 ⁇ m and 2.0 ⁇ m, the grain size distribution can be either homodisperse or heterodisperse.
  • the emulsions can also contain organic silver salts, for example silver benzotriazolate or silver behenate.
  • Two or more kinds of silver halide emulsions, which are prepared separately, can be used as a mixture.
  • the photographic emulsions can be prepared using various methods (e.g. P. Glafkides, Chimie et Physique Photographique, Paul Montel, Paris (1967), GF Duffin, Photographic Emulsion Chemistry, The Focal Press, London (1966), VL Zelikman et al, Making and Coating Photographic Emulsion, The Focal Press, London (1966) from soluble silver salts and soluble halides.
  • various methods e.g. P. Glafkides, Chimie et Physique Photographique, Paul Montel, Paris (1967), GF Duffin, Photographic Emulsion Chemistry, The Focal Press, London (1966), VL Zelikman et al, Making and Coating Photographic Emulsion, The Focal Press, London (1966) from soluble silver salts and soluble halides.
  • the silver halide is preferably precipitated in the presence of the binder, for example the gelatin, and can be carried out in the acidic, neutral or alkaline pH range, silver halide complexing agents preferably being additionally used.
  • the latter include, for example, ammonia, thioether, imidazole, ammonium thiocyanate or excess halide.
  • the water-soluble silver salts and the halides are combined either in succession by the single-jet process or simultaneously by the double-jet process or by any combination of the two processes. Prefers the dosage increases with increasing inflow rates, whereby the "critical" feed rate, at which no new germs are just emerging, should not be exceeded.
  • the pAg range can vary within wide limits during the precipitation, preferably the so-called pAg-controlled method is used, in which a certain pAg value is kept constant or a defined pAg profile is traversed during the precipitation.
  • so-called inverse precipitation with an excess of silver ions is also possible.
  • the silver halide crystals can also grow by physical ripening (Ostwald ripening) in the presence of excess halide and / or silver halide complexing agent.
  • the growth of the emulsion grains can even take place predominantly by Ostwald ripening, preferably a fine-grained, so-called Lippmann emulsion, mixed with a less soluble emulsion and redissolved on the latter.
  • Salts or complexes of metals such as Cd, Zn, Pb, Tl, Bi, Ir, Rh, Fe may also be present during the precipitation and / or physical ripening of the silver halide grains.
  • the precipitation can also be carried out in the presence of sensitizing dyes.
  • Complexing agents and / or dyes can be rendered ineffective at any time, for example by changing the pH or by an oxidative treatment.
  • Gelatin is preferably used as the binder. However, this can be replaced in whole or in part by other synthetic, semi-synthetic or naturally occurring polymers. Synthetic gelatin substitutes are, for example, polyvinyl alcohol, poly-N-vinylpyrolidone, polyacrylamides, polyacrylic acid and their derivatives, in particular their copolymers.
  • Naturally occurring gelatin substitutes are, for example, other proteins such as albumin or casein, cellulose, sugar, starch or alginates, semi-synthetic gelatin substitutes are generally modified natural products, cellulose derivatives such as hydroxyalkyl cellulose, carboxymethyl cellulose and phthalyl cellulose as well as gelatin derivatives, which are reacted with alkylating or acylating agents or by grafting of polymerizable monomers are examples of this.
  • the binders should have a sufficient amount of functional groups so that enough resistant layers can be produced by reaction with suitable hardening agents.
  • functional groups are in particular amino groups, but also carboxyl groups, hydroxyl groups and active methylene groups.
  • the gelatin which is preferably used can be obtained by acidic or alkaline digestion.
  • the production of such gelatins is described, for example, in The Science and Technology of Gelatine, published by AG Ward and A. Courts, Academic Press 1977, page 295 ff.
  • the gelatin used in each case should contain the lowest possible level of photographically active impurities (inert gelatin). High viscosity, low swelling gelatins are particularly advantageous.
  • the gelatin can be partially or completely oxidized.
  • the soluble salts are removed from the emulsion, e.g. by pasta and washing, by flakes and washing, by ultrafiltration or by ion exchangers.
  • the photographic emulsions may contain compounds to prevent fogging or to stabilize the photographic function during production, storage or photographic processing.
  • Azaindenes are particularly suitable, preferably tetra- and penta-azaindenes, in particular those which are substituted by hydroxyl or amino groups.
  • Such connections are e.g. B. von Birr, Z. Wiss. Phot. 47 (1952), pp. 2-58.
  • Salts of metals such as mercury or cadmium, aromatic sulfonic or sulfinic acids such as benzenesulfinic acid, or nitrogen-containing heterocycles such as nitrobenzimidazole, nitroindazole, (subst.) Benzotriazoles or benzothiazolium salts can also be used as antifoggants.
  • Heterocycles containing mercapto groups e.g. B.
  • mercaptobenzthiazoles mercaptobenzimidazoles, Mercaptotetrazoles, mercaptothiadiazoles, mercaptopyrimidines, these mercaptoazoles also containing a water-solubilizing group, for example a carboxyl group or sulfo group.
  • a water-solubilizing group for example a carboxyl group or sulfo group.
  • the stabilizers can be added to the silver halide emulsions before, during or after their ripening.
  • the compounds can also be added to other photographic layers which are assigned to a halogen silver layer.
  • the silver halide emulsions are usually chemically ripened, for example by the action of gold compounds or compounds of divalent sulfur.
  • the photographic emulsion layers or other hydrophilic colloid layers of the light-sensitive material produced according to the invention can contain surface-active agents for various purposes, such as coating aids, to prevent electrical charging, to improve the sliding properties, to emulsify the dispersion, to prevent adhesion and to improve the photographic characteristics (eg acceleration of development, high contrast, sensitization etc.).
  • the photographic emulsions can be spectrally sensitized using methine dyes or other dyes.
  • Particularly suitable dyes are cyanine dyes, merocyanine dyes and complex merocyanine dyes.
  • Color couplers for producing the blue-green partial color image are usually couplers of the phenol or ⁇ -naphthol type; suitable examples of this are known in the literature.
  • Color couplers for producing the yellow partial color image are generally couplers with an open-chain ketomethylene group, in particular couplers of the ⁇ -acylacetamide type; Suitable examples are ⁇ -benzoylacetanilide couplers and ⁇ -pivaloylacetanilide couplers, which are also known from the literature.
  • Color couplers for producing the purple partial color image are generally couplers of the 5-pyrazolone, indazolone or pyrazoloazole type; Suitable examples of this are described in large numbers in the literature.
  • the color couplers can be 4-equivalent couplers, but also 2-equivalent couplers.
  • the latter are derived from the 4-equivalent coupler in that they contain a substituent in the coupling site, which is split off during the coupling.
  • the 2-equivalent couplers include those that are colorless and those that have an intense inherent color have, which disappears during the color coupling or is replaced by the color of the image dye produced (mask coupler) and white couplers which, when reacted with color developer oxidation products, essentially give colorless products.
  • the 2-equivalent couplers also include couplers that contain a detachable residue at the coupling point, which is released upon reaction with color developer oxidation products and thereby either directly or after one or more further groups have been split off from the primarily split off residue (e.g. DE-A-27 03-145, DE-A-28 55 697, DE-A-31 05 026, DE-A-33 19 428), a certain desired photographic activity unfolds, for example as a development inhibitor or accelerator.
  • Examples of such 2-equivalent couplers are the known DIR couplers as well as DAR or. FAR coupler.
  • DIR, DAR or FAR couplers mainly the effectiveness of the residue released during coupling is desired and the color-forming properties of these couplers are less important, such DIR, DAR or FAR couplers are also suitable, which give essentially colorless products on coupling (DE-A-1 547 640).
  • the cleavable residue can also be a ballast residue, so that upon reaction with color developer oxidation products coupling products are obtained which are diffusible or at least have a weak or restricted mobility (US Pat. No. 4,420,556).
  • High molecular weight color couplers are described, for example, in DE-C-1 297 417, DE-A-24 07 569, DE-A-31 48 125, DE-A-32 17 200, DE-A-33 20 079, DE-A-33 24 932, DE-A-33 31 743, DE-A-33 40 376, EP-A-27 284, US-A-4 080 211.
  • the high molecular weight color couplers are usually produced by polymerizing ethylenically unsaturated monomeric color couplers. However, they can also be obtained by polyaddition or polycondensation.
  • the couplers or other compounds can be incorporated into silver halide emulsion layers by first preparing a solution, a dispersion or an emulsion of the compound in question and then adding it to the casting solution for the layer in question.
  • the selection of the suitable solvent or dispersing agent depends on the solubility of the compound.
  • Hydrophobic compounds can also be introduced into the casting solution using high-boiling solvents, so-called oil formers. Corresponding methods are described for example in US-A-2 322 027, US-A-2 801 170, US-A-2 801 171 and EP-AO 043 037.
  • oligomers or polymers instead of the high-boiling solvents, oligomers or polymers, so-called polymeric oil formers, can be used.
  • the compounds can also be introduced into the casting solution in the form of loaded latices.
  • anionic water-soluble compounds e.g. dyes
  • pickling polymers e.g. acrylic acid
  • Suitable oil formers for other couplers and other compounds are e.g. Alkyl phthalates, phosphoric acid esters, citric acid esters, benzoic acid esters, alkylamides, fatty acid esters and trimesic acid esters.
  • Each of the light-sensitive layers can consist of a single layer or can also comprise two or more silver halide emulsion partial layers (DE-C-1 121 470).
  • the red-sensitive silver halide emulsion layers can be arranged closer to the support than the green-sensitive silver halide emulsion layers and these in turn closer than the blue-sensitive layers, a non-light-sensitive yellow filter layer generally being located between green-sensitive layers and blue-sensitive layers.
  • the green or Red-sensitive layers can be chosen without the yellow filter layer, other layer arrangements in which e.g. the blue-sensitive, then the green-sensitive and finally the red-sensitive layers follow.
  • the non-light-sensitive intermediate layers which are generally arranged between layers of different spectral sensitivity, can contain agents which prevent an undesired diffusion of developer oxidation products from one light-sensitive layer into another light-sensitive layer with different spectral sensitization.
  • sub-layers of the same spectral sensitization can differ with regard to their composition, in particular with regard to the type and amount of the silver halide grains.
  • the sublayer with higher sensitivity will be located further away from the support than the sublayer with lower sensitivity.
  • Partial layers of the same spectral sensitization can be adjacent to one another or separated by other layers, for example by layers of different spectral sensitization.
  • all highly sensitive and all low-sensitive layers can be combined to form a layer package (DE-A 1 958 709, DE-A 2 530 645, DE-A 2 622 922).
  • the photographic material may further contain whites, spacers, formalin scavengers and others.
  • Suitable whiteners are e.g. in Research Disclosure December 1978, page 22 ff, Unit 17 643, Chapter V.
  • binder layers in particular the most distant layer from the support, but also occasionally intermediate layers, especially if they are the most distant layer from the support during manufacture, may contain photographically inert particles of inorganic or organic nature, e.g. as a matting agent or as a spacer (DE-A 3 331 542, DE-A 3 424 893, Research Disclosure December 1978, page 22 ff, Unit 17 643, Chapter XVI).
  • photographically inert particles of inorganic or organic nature e.g. as a matting agent or as a spacer (DE-A 3 331 542, DE-A 3 424 893, Research Disclosure December 1978, page 22 ff, Unit 17 643, Chapter XVI).
  • the average particle diameter of the spacers is in particular in the range from 0.2 to 10 ⁇ m.
  • the spacers are water-insoluble and can be alkali-insoluble or alkali-soluble, the alkali-soluble ones generally being removed from the photographic material in the alkaline development bath.
  • suitable polymers are polymethyl methacrylate, copolymers of acrylic acid and methyl methacrylate and hydroxypropyl methyl cellulose hexahydrophthalate.
  • polyethylene-coated paper can be used as a reflective support.
  • the color photographic recording material according to the invention is developed with a color developer compound.
  • All developer compounds which have the ability to react in the form of their oxidation product with color couplers to form azomethine dyes can be used as the color developer compound.
  • Suitable color developer compounds are aromatic compounds of the p-phenylenediamine type containing at least one primary amino group, for example N, N-dialkyl-p-phenylenediamines, such as N, N-diethyl-p-phenylenediamine, 1- (N-ethyl-N-methylsulfonamidoethyl) -3 -methyl-p-phenylenediamine, 1- (N-ethyl-N-hydroxyethyl-3-methyl-p-phenylenediamine and 1- (N-ethyl-N-methoxyethyl) -3-methyl-p-phenylenediamine.
  • N, N-dialkyl-p-phenylenediamines such as N, N-diethyl-p-phenylenediamine, 1- (N-ethyl-N-methylsulfonamidoethyl) -3 -methyl-p-phenylenediamine, 1- (N-eth
  • the recording material according to the invention is particularly suitable for processing in an abbreviated processing process, for example in a processing process whose development step at temperatures between 25 and 45 ° C. lasts less than 3 minutes, preferably less than 1 minute. Particularly when developing with developer baths free of benzyl alcohol, advantageous results are obtained.
  • the color developer solution preferably contains ⁇ 0.01 mol / l bromide and ⁇ 5 ml / l benzyl alcohol.
  • the material is usually bleached and fixed. Bleaching and fixing can be carried out separately or together.
  • the usual compounds can be used as bleaching agents, e.g. Fe3+ salts and Fe3+ complex salts such as ferricyanides, dichromates, water-soluble cobalt complexes, etc.
  • Particularly preferred are iron III complexes of aminopolycarboxylic acids, in particular e.g. Ethylenediaminetetraacetic acid, N-hydroxyethylethylenediamine triacetic acid, alkyliminodicarboxylic acids and corresponding phosphonic acids.
  • Persulphates are also suitable as bleaching agents.
  • compositions and processing times of the developing and bleach-fixing bath in which the material according to the invention is processed are given below. Watering is followed by usual drying.
  • the material can also be treated with a conventional stabilizing bath.
  • a color photographic recording material which is suitable for a rapid processing process was produced by applying the following layers in the order given to a support on paper coated on both sides with polyethylene.
  • the quantities given relate to 1 m2.
  • the corresponding amounts of AgNO3 are given.
  • UV-15 is used as a UV absorber with 0.4 g DBP as an oil former.
  • 0.15 g UV-15 with 0.1 g DBP are used.
  • 0.4 g UV-15 and 0.2 g UV-9 with 0.4 g DBP are used as oil formers and in layer 7 0.1 g UV-15 with 0.05 g UV-9 with 0 , 1 g DBP used.
  • the five structures are exposed behind a blue color separation filter with a 3 / 2 wedge and developed according to the above information.
  • the yellow color separation wedges obtained are measured with a densitometer, thereby determining sensitivity, shoulder gradation and maximum color density. The results are shown in the following overview:
  • a wedge in which all three color separations were exposed in such a way that a neutral gray wedge was obtained showed in the yellow the gradation and density in the same way depending on the UV layer composition.
  • the maximum density of purple was also 0.1 - 0.2 higher for superstructures 2 - 5.
  • UV layers composed according to the invention result in a substantially better color density in the color structures.

Claims (9)

  1. Matériau photographique en couleurs à l'halogénure d'argent, qui est durci par un durcisseur immédiat et qui contient sur un support au moins une couche d'émulsion d'halogénure d'argent dont les grains d'halogénure d'argent contiennent au moins 80 mol% de chlorure d'argent et au moins une couche qui contient une substance absorbant la lumière ultraviolette, qui est liquide à 15°C.
  2. Matériau photographique en couleurs selon la revendication 1, caractérisé en ce qu'il contient au moins une couche sensible au bleu à laquelle est associé un coupleur pour jaune, au moins une couche sensible au vert à laquelle est associé au moins un coupleur pour magenta et au moins une couche sensible au rouge à laquelle est associé un coupleur pour cyan.
  3. Matériau photographique en couleurs selon la revendication 1, caractérisé en ce qu'il contient un support réfléchissant.
  4. Matériau photographique en couleurs selon la revendication 1, caractérisé en ce que les halogénures d'argent de toutes les couches photosensibles contiennent au moins 80 mol% de chlorure.
  5. Matériau photographique en couleurs selon la revendication 1, caractérisé en ce que les halogénures d'argent de toutes les couches photosensibles contiennent 95 à 100 mol% de chlorure, 0 à 5 mol% de bromure et 0 à 1 mol% d'iodure.
  6. Matériau photographique en couleurs selon la revendication 1, caractérisé en ce que les absorbeurs d'UV liquides répondent à la formule générale :
    Figure imgb0194
     dans laquelle
    R₁ et R₂   représentent chacun un groupe alkyle, aryle, alcoxy ou aryloxy et
    R₃   représente un atome d'hydrogène ou d'halogène ou un groupe alkyle, aryle, alcoxy, aryloxy, alcényle, nitro ou hydroxy.
  7. Matériau photographique en couleurs selon la revendication 6, dans lequel les substituants R₁, R₂ et R₃ présentent les combinaisons de définitions I, II, III, IV et V suivantes :
    I:   R₁: méthyle, éthyle, propyle,
    R₂ : sec-alkyle en C₄-C₁₂,
    R₃ : hydrogène, halogène, alkyle en C₁-C₈, alcoxy en C₁-C₈,
    II :   R₁, R₂ et R₃ : alkyle en C₄-C₁₂, l'un d'eux étant un reste sec-alkyle,
    III:   R₁: alkyle en C₁-C₁₂,
    R₂ : (alcoxy en C₁-C₁₂)carbonyl-alkyle en C₁-C₆,
    R₃ : hydrogène, halogène, alkyle en C₁-C₈, alcoxy en C₁-C₈,
    IV:   R₁, R₂ : sec-alkyle en C₄-C₁₂,
    R₃ : hydrogène, halogène, alkyle en C₁-C₈, alcoxy en C₁-C₈,
    V:   R₁: alkyle en C₁₀-C₁₅ ramifié,
    R₂ : alkyle en C₁-C₄,
    R₃ : hydrogène, halogène, alkyle en C₁-C₈, alcoxy en C₁-C₈.
  8. Matériau photographique en couleurs selon la revendication 1, caractérisé en ce que le durcisseur immédiat répond à la formule générale :
    Figure imgb0195
     dans laquelle
    R₁   représente un groupe alkyle, aryle ou aralkyle,
    R₂   a la même signification que R₁ ou représente un groupe alkylène, arylène, aralkylène ou alcaralkylène, la seconde liaison étant reliée à un groupe de formule :
    Figure imgb0196
    ou bien
    R₁ et R₂   représentent ensemble les atomes nécessaires pour compléter un noyau hétérocyclique éventuellement substitué, par exemple, un noyau pipéridine, pipérazine ou morpholine, le noyau pouvant être substitué par exemple par alkyle en C₁-C₃ ou halogène,
    R₃   représente un atome d'hydrogène ou un groupe alkyle, aryle, alcoxy, -NR₄-COR₅, -(CH₂)m-NR₈R₉, -(CH₂)n-CONR₁₃R₁₄ ou
    Figure imgb0197
     ou un chaînon de pontage ou une liaison directe sur une chaîne polymère, dans lesquels
    R₅   représente un atome d'hydrogène ou un groupe alkyle en C₁-C₄ ou -NR₆R₇,
    R₈   représente un groupe -COR₁₀
    R₁₀   représente un groupe -NR₁₁R₁₂
    R₁₁   représente un groupe alkyle en C₁-C₄ ou aryle, en particulier phényle,
    R₁₂   représente un atome d'hydrogène ou un groupe alkyle en C₁-C₄ ou aryle, en particulier phényle,
    R₁₃   représente un atome d'hydrogène ou un groupe alkyle en C₁-C₄ ou aryle, en particulier phényle,
    R₁₆   représente un atome d'hydrogène ou un groupe alkyle en C₁-C₄,-COR₁₈ ou -CONHR₁₉,
    m   est un nombre de 1 à 3,
    n   est un nombre de 0 à 3,
    p   est un nombre de 2 à 3 et
    Y   représente -O- ou 〉NR₁₇,
    R₄, R₆, R₇, R₉, R₁₄, R₁₅, R₁₇, R₁₈ et R₁₉ représentent un atome d'hydrogène ou un groupe alkyle en C₁-C₄,
    R₁₃ et R₁₄,   pris ensemble, représentent les atomes nécessaires pour compléter un noyau hétérocyclique éventuellement substitué, par exemple un noyau pipéridine, pipérazine ou morpholine, le noyau pouvant être substitué par exemple par alkyle en C₁-C₃ ou halogène,
    Z   représente les atomes de carbone nécessaires pour compléter un noyau hétérocyclique aromatique à 5 ou 6 chaînons, éventuellement condensé avec un noyau benzénique, et
    X⊖   représente un anion qui peut être relié par une liaison covalente au reste de la molécule.
  9. Matériau photographique en couleurs selon la revendication 1, caractérisé en ce que le durcisseur immédiat est utilisé en quantité de 0,1 à 5 mmol/m².
EP89109108A 1988-06-04 1989-05-20 Matériau photographique couleur à l'halogénure d'argent Expired - Lifetime EP0345514B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3819082 1988-06-04
DE3819082A DE3819082A1 (de) 1988-06-04 1988-06-04 Farbfotografisches silberhalogenidmaterial

Publications (3)

Publication Number Publication Date
EP0345514A2 EP0345514A2 (fr) 1989-12-13
EP0345514A3 EP0345514A3 (en) 1990-09-26
EP0345514B1 true EP0345514B1 (fr) 1994-08-31

Family

ID=6355882

Family Applications (1)

Application Number Title Priority Date Filing Date
EP89109108A Expired - Lifetime EP0345514B1 (fr) 1988-06-04 1989-05-20 Matériau photographique couleur à l'halogénure d'argent

Country Status (3)

Country Link
EP (1) EP0345514B1 (fr)
JP (1) JPH0237339A (fr)
DE (2) DE3819082A1 (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5601971A (en) * 1991-06-18 1997-02-11 Sterling Diagnsotic Imaging, Inc. Hardening of hydrophilic colloids with imidazolium and triazine combinations
DE4119982C2 (de) * 1991-06-18 1993-09-30 Du Pont Deutschland 1,3-Bis-carbamoylimidazoliumverbindungen und Verfahren zum Härten von Gelatine enthaltenden Schichten
KR100833057B1 (ko) * 2005-11-23 2008-05-27 주식회사 엘지화학 관형 고정층 촉매 반응기에서 온도를 측정하는 도구 및방법
US10574014B2 (en) 2017-03-27 2020-02-25 Aptiv Technologies Limited Method for sealing electric terminal assembly
US10017659B1 (en) 2017-10-09 2018-07-10 Delphi Technologies, Inc Robust sealed electric terminal assembly

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2439551C2 (de) * 1974-08-17 1985-11-21 Agfa-Gevaert Ag, 5090 Leverkusen Verfahren zur Härtung photographischer Schichten
DE3781311T2 (de) * 1986-04-24 1993-04-01 Konishiroku Photo Ind Lichtempfindliches photographisches silberhalogenidmaterial.
DE3744004A1 (de) * 1987-12-24 1989-07-06 Agfa Gevaert Ag Farbfotografisches aufzeichnungsmaterial und verfahren zur herstellung einer fotografischen silberhalogenidemulsion

Also Published As

Publication number Publication date
JPH0237339A (ja) 1990-02-07
DE3819082A1 (de) 1989-12-14
DE58908257D1 (de) 1994-10-06
EP0345514A3 (en) 1990-09-26
EP0345514A2 (fr) 1989-12-13

Similar Documents

Publication Publication Date Title
DE3736410A1 (de) Farbfotografisches silberhalogenidmaterial
EP0358071B1 (fr) Matériau de reproduction photographique
EP0345514B1 (fr) Matériau photographique couleur à l'halogénure d'argent
EP0537545B1 (fr) Produit photographique à l'halogénure d'argent
EP0351588B1 (fr) Matériau de reproduction photographique couleur
EP0370226B1 (fr) Matériel photographique à l'halogénure d'argent et sa méthode de traitement
EP0607801A1 (fr) Matériau photographique couleur d'enregistrement
EP0363820A2 (fr) Matériau photographique couleur à l'halogénure d'argent
EP0377889B1 (fr) Matériel d'enregistrement à l'halogénure d'argent
EP0607800A1 (fr) Matériau photographique couleur d'enregistrement
EP0369235B1 (fr) Matériau d'enregistrement photographique
DE4318438A1 (de) Fotografisches Aufzeichnungsmaterial
EP0345553B1 (fr) Matériau de reproduction photographique
EP0373339B1 (fr) Matériau d'enregistrement photosensible à l'halogénure d'argent
EP0377181A2 (fr) Matériau photographique couleur
DE4320828A1 (de) Farbfotografisches Aufzeichnungsmaterial
EP0312837A2 (fr) Procédé de traitement photographique sans lavage à l'eau et bain de stabilisation utilisé pour ce procédé
EP0317825B1 (fr) Matériau de reproduction photographique couleur
DE3744004A1 (de) Farbfotografisches aufzeichnungsmaterial und verfahren zur herstellung einer fotografischen silberhalogenidemulsion
EP0267523B1 (fr) Matériau photographique couleur à l'halogénure d'argent sensible à la lumière
EP0447657B1 (fr) Matériau d'enregistrement photographique
DE3806629A1 (de) Verfahren zur erzeugung von colorbildern
DE3838467A1 (de) Fotografisches aufzeichnungsmaterial
EP0286913A2 (fr) Matériau d'enregistrement photographique couleur
EP0616256A1 (fr) Matériau photographique couleur d'enregistrement

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19890520

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): DE FR GB NL

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): DE FR GB NL

17Q First examination report despatched

Effective date: 19930804

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR GB NL

REF Corresponds to:

Ref document number: 58908257

Country of ref document: DE

Date of ref document: 19941006

GBT Gb: translation of ep patent filed (gb section 77(6)(a)/1977)

Effective date: 19941028

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
REG Reference to a national code

Ref country code: GB

Ref legal event code: 746

Effective date: 19951016

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19980414

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19980511

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 19980520

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19980531

Year of fee payment: 10

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19990520

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19991201

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 19990520

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20000131

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 19991201

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20000301

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST