EP0154920B1 - Emulsion à haute teneur en chlorure d'argent, matériel photographique pour l'enregistrement et procédé pour réaliser un enregistrement photographique - Google Patents

Emulsion à haute teneur en chlorure d'argent, matériel photographique pour l'enregistrement et procédé pour réaliser un enregistrement photographique Download PDF

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Publication number
EP0154920B1
EP0154920B1 EP85102439A EP85102439A EP0154920B1 EP 0154920 B1 EP0154920 B1 EP 0154920B1 EP 85102439 A EP85102439 A EP 85102439A EP 85102439 A EP85102439 A EP 85102439A EP 0154920 B1 EP0154920 B1 EP 0154920B1
Authority
EP
European Patent Office
Prior art keywords
silver halide
photographic
mol
emulsion
halide emulsion
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
Application number
EP85102439A
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German (de)
English (en)
Other versions
EP0154920A2 (fr
EP0154920A3 (en
Inventor
Sieghart Dipl.-Ing. Klötzer
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
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Agfa Gevaert AG
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Filing date
Publication date
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Publication of EP0154920A2 publication Critical patent/EP0154920A2/fr
Publication of EP0154920A3 publication Critical patent/EP0154920A3/de
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Publication of EP0154920B1 publication Critical patent/EP0154920B1/fr
Expired legal-status Critical Current

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Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/005—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
    • G03C1/035—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein characterised by the crystal form or composition, e.g. mixed grain
    • G03C2001/03535—Core-shell grains

Definitions

  • the invention relates to an emulsion rich in silver chloride, a photographic recording material and a method for producing photographic recordings.
  • Silver halide emulsions which contain chloride, bromide, iodide or mixtures thereof as the halide.
  • Silver bromide and silver bromide iodide emulsions are generally used for more sensitive recording materials.
  • a disadvantage of the last-mentioned emulsions is that they have an intrinsic sensitivity in the blue spectral range. Therefore, in color recording materials, green and red sensitive layers are generally placed behind a filter that absorbs blue light. Furthermore, such emulsions cannot be developed as quickly as silver chloride emulsions.
  • Chloride-containing silver halide emulsions are also known, the grains of which have a layered structure. Such grains have a core and at least one layer which surrounds the core and whose properties differ from the core. From DE-AS-1 169 290 and GB-1 027 146 it is known to coat a silver chloride shell on a silver bromide core.
  • DE-OS-2 308 239 and US-3,935,014 relate to emulsions for producing directly positive images with silver halide grains which have a localized phase with a high silver chloride content.
  • a photographic silver halide emulsion which essentially contains chloride as the halide and whose grains have a layered grain structure composed of at least two areas of different halide composition - e.g. B. a core and at least one shell - have.
  • the area B can be present both as a core and as a shell around a core.
  • the region B contains AgCI and optionally Agl, preferably up to a maximum of 10%.
  • the grains preferably contain a core enveloped by at least one region B. In this case, region B can be present as a shell within the silver halide grain or on the surface of the crystal.
  • the crystal nucleus is successively provided with two shells containing silver bromide, the bromide content of the two shells being significantly different.
  • a bromide-containing shell with a local concentration of 30 to 45 mol.-0 / o bromide is preferably located on the crystal surface of the chloride-rich silver halide crystal.
  • the bromide concentration is 3 to 8 mol%, based on the total halide.
  • the silver halide grains can have chloride, bromide, iodide or mixtures thereof in the core and in the areas other than halide.
  • the transition from one area to an adjacent area of a different composition can be sharp or continuous.
  • the chloride content of the total halide content is at least 85, in particular at least 90, mol%.
  • the silver halide emulsions according to the invention can be prepared by means of the customary procedures (eg single entry, double entry, with constant or accelerated material flow). It is particularly preferred to use the double-inlet process under control of the pAg value.
  • the precipitation can be carried out in the presence of conventional dopants, e.g. B. in the presence of Ir compounds.
  • the silver halide grains can be designed, for example, as cubes, octahedra or tetradecahedra.
  • the grain size is preferably between 0.1 and 2.5 J.1m, in particular between 0.2 and 1.0 ⁇ m.
  • the emulsion has a narrow grain size distribution.
  • at least 95% by weight of the grains have a diameter which does not deviate from the average grain diameter by more than 40%.
  • the emulsions can also have a broad grain size distribution.
  • at least 10%, preferably 20%, of the silver halide grains have a diameter which deviates from the average grain diameter by at least 40%.
  • the present invention further relates to a photographic recording material which contains at least one silver halide emulsion layer according to the invention on a support.
  • the invention further relates to a method for producing photographic recordings by developing an exposed recording material according to the invention.
  • the emulsions according to the invention are preferably chemically sensitized to a high surface sensitivity on the grain surface. They can be chemically sensitized using known methods, e.g. B. with active gelatin or with compounds of sulfur, selenium, tellurium, gold, palladium, platinum, iridium, the pAg values between 4 and 10, the pH values between 3.5 and 9 and the temperatures between 30 ° C. and can fluctuate 90 ° C; chemical sensitization can be carried out in the presence of heterocyclic nitrogen compounds such as imidazoles, azaindenes, azapyridazines and azapyrimidines and thiocyanate derivatives, thioethers and other silver halide solvents.
  • heterocyclic nitrogen compounds such as imidazoles, azaindenes, azapyridazines and azapyrimidines and thiocyanate derivatives, thioethers and other silver halide solvents.
  • the emulsions according to the invention can be subjected to a reduction sensitization, e.g. B. by hydrogen, by low pAg (z. B. less than 5) and / or high pH (z. B. above 8), by reducing agents such as tin (II) chloride, thiourea dioxide and aminoborane.
  • a reduction sensitization e.g. B. by hydrogen
  • low pAg z. B. less than 5
  • high pH z. B. above 8
  • reducing agents such as tin (II) chloride, thiourea dioxide and aminoborane.
  • the surface ripening nuclei can also be present as troglodyte nuclei (sub-surface nuclei) according to DE-OS-2 306 447 and US Pat. No. 3,966,476. If necessary, the grains can also be matured inside. Other methods are described in the above. Research Disclosure No. 17643 in Section 111.
  • the emulsions can be optically sensitized in a manner known per se, e.g. B. with the usual polymethine dyes such as neutrocyanines, basic or acid carbocyanines, rhodacyanines, hemicyanines, styryl dyes, oxonols and the like.
  • polymethine dyes such as neutrocyanines, basic or acid carbocyanines, rhodacyanines, hemicyanines, styryl dyes, oxonols and the like.
  • Such sensitizers are from F.M. Hamer in "The Cyanine Dyes and related Compounds", (1964).
  • EP-A-0 082 649 and in particular to Ullmann's Encyclopedia of Industrial Chemistry, 4th edition, volume 18, pages 431 ff and to Research Disclosure No. 17643, section IV indicated above.
  • the spectral sensitization can be too at any time during the preparation of the emulsion, d
  • the commonly used antifoggants and stabilizers can be used.
  • Suitable stabilizers are azaindenes, preferably tetra- or penta-azaindenes, in particular those which are substituted by hydroxyl or amino groups. Such connections are e.g. B. in the article by Birr, Z.Wiss.Phot. 47, 1952), pp. 2-58. Other suitable stabilizers and antifoggants are given in Research Disclosure No. 17643 above in Section IV.
  • the recording material according to the invention is preferably a color photographic recording material.
  • the color image is generated using color couplers. It is possible to let the color coupler diffuse into the recording material only during development.
  • the photographic material itself contains the usual color couplers, which can react with the oxidation product of developers, generally p-phenylenediamines, to form dyes.
  • the red-sensitive layer can contain a non-diffusing color coupler for producing the blue-green partial color image, usually a coupler of the phenol or a-naphthol type.
  • the green-sensitive layer can contain, for example, at least one non-diffusing color coupler for producing the purple partial color image, color couplers of the 5-pyrazolone type usually being used.
  • the blue-sensitive layer can contain, for example, a non-diffusing color coupler for generating the yellow partial color image, usually a color coupler with an open-chain ketomethylene grouping.
  • a color coupler with an open-chain ketomethylene grouping usually a color coupler with an open-chain ketomethylene grouping.
  • the color couplers it can be, for. B. are 6-, 4- and 2-equivalent couplers, including the so-called white couplers, which do not give any dye when reacted with color developer oxidation products.
  • Suitable couplers are known, for example, from the publications "Color Coupler" by W. Pelz in "Messages from the Research Laboratories of Agfa, Leverkusen / Kunststoff", Volume 111, page 111 (1961), K. Venkataraman in "The Chemistry of Synthetic Dyes", Vol. 4, 341 to 387, Academic Press (1971) and TH James, “The Theory of the Photographic Process", 4th Ed., Pp. 353-362
  • the recording material can also contain DIR compounds.
  • DIR compounds are understood to mean those compounds which, when reacted with color developer oxidation products, release diffusing organic compounds which inhibit the development of silver halide.
  • the inhibitors can be eliminated directly or via non-inhibiting intermediates. Reference is made to GB-953 454, US-3 632 345, US-4 248 962 and GB-2 072 363.
  • the color couplers and DIR compounds can be incorporated into the materials according to the invention by customary, known methods. If the compounds are soluble in water or alkali, they can be added in the form of aqueous solutions, optionally with the addition of water-miscible organic solvents such as ethanol, acetone or dimethylformamide. Insofar as the color couplers and DIR connectors are insoluble in water or alkali, they can be prepared in a manner known per se dispersed form can be incorporated into the recording materials. For example, a solution of these compounds in a low-boiling organic solvent can be mixed directly with the silver halide emulsion or initially with an aqueous gelatin solution and the organic solvent can then be removed.
  • a solution of these compounds in a low-boiling organic solvent can be mixed directly with the silver halide emulsion or initially with an aqueous gelatin solution and the organic solvent can then be removed.
  • the dispersion of the respective compound thus obtained can then be mixed with the silver halide emulsion.
  • so-called oil formers are also used, usually higher-boiling organic compounds, which include the color couplers and DIR compounds to be dispersed in the form of oily droplets.
  • oil formers usually higher-boiling organic compounds, which include the color couplers and DIR compounds to be dispersed in the form of oily droplets.
  • the recording materials according to the invention preferably contain at least one silver halide emulsion layer unit for recording blue, green and red light.
  • the red-sensitive silver halide emulsion layer unit can be arranged closer to the layer support than the green-sensitive silver halide emulsion layer unit and this in turn can be arranged closer than the blue-sensitive one. In the case of copying materials in particular, however, the position of the blue and red sensitive layers can also be interchanged.
  • the recording material may optionally contain a yellow filter layer; However, this can be dispensed with in particular if at least the red- and green-sensitive layers contain an emulsion according to the invention.
  • At least one of the units for recording green, red and blue light consists of at least two sub-layers. It is possible to combine sub-layers of different spectral sensitization according to their sensitivity.
  • the usual substrates can be used for the materials according to the invention, e.g. B. carriers made of cellulose esters, for. B. cellulose acetate and polyester. Also suitable are paper supports, which can optionally be coated, for. B. with polyolefins, especially with polyethylene or polypropylene.
  • B. carriers made of cellulose esters, for. B. cellulose acetate and polyester.
  • paper supports which can optionally be coated, for. B. with polyolefins, especially with polyethylene or polypropylene.
  • polyolefins especially with polyethylene or polypropylene.
  • hydrophilic film-forming agents are suitable as protective colloid or binder for the layers of the recording material, e.g. B. proteins, especially gelatin, alginic acid or their derivatives such as esters, amides or salts, cellulose derivatives such as carboxymethyl cellulose and cellulose sulfates, starch or their derivatives or hydrophilic synthetic binders such as polyvinyl alcohol, partially saponified polyvinyl acetate, polyvinyl pyrrolidone and others.
  • B. proteins especially gelatin, alginic acid or their derivatives such as esters, amides or salts, cellulose derivatives such as carboxymethyl cellulose and cellulose sulfates, starch or their derivatives or hydrophilic synthetic binders such as polyvinyl alcohol, partially saponified polyvinyl acetate, polyvinyl pyrrolidone and others.
  • the layers can also contain other synthetic binders in dissolved or dispersed form, such as homopolymers or copolymers of acrylic or methacrylic acid or their derivatives, such as esters, amides or nitriles, and also vinyl polymers, such as vinyl esters or vinyl ethers.
  • binders specified in Research Disclosure 17643 above in Section IX.
  • the layers of the photographic material can be hardened in the usual manner, for example with hardeners of the epoxy type, the heterocyclic ethylene imine and the acryloyl type. Furthermore, it is also possible to harden the layers in accordance with the process of German laid-open specification 2 218 009 in order to obtain color photographic materials which are suitable for high-temperature processing. It is also possible to harden the photographic layers or the color photographic multilayer materials with hardeners of the diazine, triazine or 1,2-dihydroquinoline series or with hardeners of the vinyl sulfone type. Further suitable hardening agents are known from German laid-open documents 2 439 551, 2 225 230, 2 317 672 and from Research Disclosure 17643, section XI given above.
  • the photographic materials according to the invention may also contain other substances, in particular plasticizers, wetting agents, screen dyes, light scattering agents, light reflecting agents, lubricants, antistatic agents, matting agents, etc.
  • plasticizers in particular plasticizers, wetting agents, screen dyes, light scattering agents, light reflecting agents, lubricants, antistatic agents, matting agents, etc.
  • Suitable color developer substances for the material according to the invention are in particular those of the p-phenylenediamine type, e.g. B. 4-amino-N, N-diethyl-aniline hydrochloride; 4-amino-3-methyl-N-ethyl-N- ⁇ - (methanesulfonamido) ethylaniline sulfate hydrate; 4-amino-3-methyl-N-ethyl-N- ⁇ -hydroxyethylaniline sulfate; 4-amino-N-ethyl-N- (2-methoxyethyl) -m-toluidine-di-p-toluenesulfonic acid and N-ethyl-N-ß-hydroxyethyl-p-phenylenediamine.
  • B 4-amino-N, N-diethyl-aniline hydrochloride; 4-amino-3-methyl-N-ethyl-N- ⁇ - (
  • color developers are described, for example, in J.Amer.Chem.Soc. 73, 3100 (1951) and in G. Haist, Modern Photographic Processing, 1979, John Wiley and Sons, New York, pages 545 ff.
  • the color developers may contain the usual other ingredients, e.g. B. lime and antioxidants and anti-fogging agents such. B. bromide or stabilizers known per se.
  • 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. B. Fe 3 + salts and Fe 3 + - complex salts such as ferricyanides, dichromates, water-soluble cobalt complexes, etc.
  • Particularly preferred are iron III complexes of aminopolycarboxylic acids, especially z.
  • Persulphates are also suitable as bleaching agents.
  • a silver chloride emulsion is produced within 25 minutes by pAg-controlled double entry of a 0.3 N NaCl and a 0.3 N AgNO 3 solution to a 2.5% gelatin solution brought to a temperature of 55 ° C.
  • the average particle size is 0.15 ⁇ m and the emulsion has a monodisperse distribution.
  • the crystals of this starting emulsion are enlarged to 36 times the volume by further addition of 2 n NaCl and 2 n AgNO 3 solutions.
  • the pAg value is kept constant at 6.8.
  • the crystals of the emulsion produced in this way have a monodisperse particle size distribution and an average particle diameter of 0.53 ⁇ m; the volume fraction of the Br / CI shell is 10% based on the total volume of the silver halide crystals.
  • the AgBr content is 4 mol%, based on the total halide.
  • a silver halide emulsion such as emulsion A is prepared by pAg-controlled double enema.
  • the KBr / NaCI solution is replaced by a pure KBr solution of identical concentration.
  • An AgBr shell is applied to the silver chloride crystals by controlled double entry in such a way that the bromide concentration is 5 mol%, based on the total halide.
  • the average particle diameter of the emulsion produced in this way is 0.55 ⁇ m and the crystals have a monodisperse particle size distribution.
  • Emulsions A and B are freed from the soluble salts by flocculation and washing in the usual way and then adjusted to a pAg of 7.6. All emulsions are then chemically sensitized by adding sodium thiosulfate at 55 ° C for 120 minutes. For the sensitometric test, the ripened emulsions are mixed with a sensi dye that absorbs in the green spectral range and a usual magenta coupler emulsate and applied to a layer support, the silver application being kept constant for all layers.
  • Table 1 shows the significantly higher sensitivity and a steeper gradation with an otherwise identical sensitometry.
  • both emulsions are mixed with a sensi dye that absorbs in the blue spectral range and a conventional yellow coupler emulsate and applied to a layer carrier with a silver coating corresponding to 3.2 g AgN0 3 per m 2 .

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  • Chemical & Material Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)

Claims (12)

1. Emulsion d'halogénure d'argent photographique contenant essentiellement, en tant qu'halogénure, le chlorure, et dont les grains ont une structure lamellaire, caractérisée en ce que:
1. au moins 60 mol.-% de l'halogénure d'argent de l'émulsion consistent en chlorure d'argent, et
2. au moins une région B contient au moins 10 mol.-% d'AgBr mais moins de 50 mol.-% d'AgBr.
2. Emulsion d'halogénure d'argent photographique selon la revendication 1, caractérisée en ce que les grains comportent un noyau enrobé dans au moins une région B.
3. Emulsion d'halogénure d'argent photographique selon la revendication 1, caractérisée en ce que 85 mol.- % au moins de l'halogénure total consistent en chlorure d'argent.
4. Emulsion d'halogénure d'argent photographique selon la revendication 2, caractérisée en ce que la région B contient au moins 25 mol.-% de bromure d'argent.
5. Emulsion d'halogénure d'argent photographique selon la revendication 1, caractérisée en ce que la dimension de grain moyenne se situe entre 0,1 et 2,5 µm.
6. Emulsion d'halogénure d'argent photographique selon la revendication 1, caractérisée en ce qu'elle présente une répartition étroite des dimensions de grains.
7. Emulsion d'halogénure d'argent photographique selon la revendication 1, caractérisée en ce qu'elle présente une large répartition des dimensions de grains.
8. Emulsion d'halogénure d'argent photographique selon la revendication 1, caractérisée en ce que les grains sont sensibilisés chimiquement et/ou ont été soumis à sensibilisation spectrale en surface.
9. Matériau d'enregistrement photographique comprenant un support et au moins une couche d'émulsion d'halogénure d'argent appliquée sur ce support, caractérisé en ce qu'il contient au moins une émulsion selon la revendication 1.
10. Procédé pour obtenir des enregistrements photographiques par développement d'un matériau d'enregistrement exposé à la lumière, caractérisé en ce que l'on utilise le matériau d'enregistrement selon la revendication 9.
EP85102439A 1984-03-15 1985-03-05 Emulsion à haute teneur en chlorure d'argent, matériel photographique pour l'enregistrement et procédé pour réaliser un enregistrement photographique Expired EP0154920B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19843409445 DE3409445A1 (de) 1984-03-15 1984-03-15 Silberchloridreiche emulsion, fotografisches aufzeichnungsmaterial und verfahren zur herstellung fotografischer aufzeichnungen
DE3409445 1984-03-15

Publications (3)

Publication Number Publication Date
EP0154920A2 EP0154920A2 (fr) 1985-09-18
EP0154920A3 EP0154920A3 (en) 1988-01-13
EP0154920B1 true EP0154920B1 (fr) 1989-01-04

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EP85102439A Expired EP0154920B1 (fr) 1984-03-15 1985-03-05 Emulsion à haute teneur en chlorure d'argent, matériel photographique pour l'enregistrement et procédé pour réaliser un enregistrement photographique

Country Status (4)

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US (1) US4605610A (fr)
EP (1) EP0154920B1 (fr)
JP (1) JPS60222845A (fr)
DE (2) DE3409445A1 (fr)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62194252A (ja) * 1986-02-20 1987-08-26 Fuji Photo Film Co Ltd カラ−画像形成方法
DE3606086A1 (de) * 1986-02-26 1987-08-27 Agfa Gevaert Ag Farbfotografisches aufzeichnungsmaterial
JP2561088B2 (ja) * 1986-04-25 1996-12-04 コニカ株式会社 ハロゲン化銀カラー写真感光材料
JPH07113741B2 (ja) * 1986-04-26 1995-12-06 コニカ株式会社 高感度で経時保存性が改善されたハロゲン化銀カラ−写真感光材料
JP2530861B2 (ja) * 1986-07-31 1996-09-04 コニカ株式会社 迅速処理可能なハロゲン化銀写真感光材料
JP2627150B2 (ja) * 1986-07-31 1997-07-02 コニカ株式会社 迅速処理可能なハロゲン化銀カラー写真感光材料
EP0256537B1 (fr) * 1986-08-15 1992-12-30 Fuji Photo Film Co., Ltd. Epreuve couleur et méthode pour sa production
JPS6363044A (ja) * 1986-09-04 1988-03-19 Fuji Photo Film Co Ltd カラ−画像形成方法
DE3787088T2 (de) * 1986-12-26 1993-12-09 Fuji Photo Film Co Ltd Photographische Emulsionen mit Silberhalogenid vom Eckenentwicklungstyp.
EP0273430B1 (fr) * 1986-12-26 1993-03-17 Fuji Photo Film Co., Ltd. Matériaux photographiques à l'halogénure d'argent et procédé de production de ceux-ci
JPH07119937B2 (ja) * 1986-12-26 1995-12-20 富士写真フイルム株式会社 ハロゲン化銀写真感光材料
JPH0738068B2 (ja) * 1986-12-26 1995-04-26 富士写真フイルム株式会社 写真感光材料およびその現像処理方法
JPS646942A (en) * 1987-02-28 1989-01-11 Konishiroku Photo Ind Production of photographic sensitive silver halide emulsion
JPS6444938A (en) * 1987-08-13 1989-02-17 Fuji Photo Film Co Ltd Method for forming amplification of color image
JPH0734103B2 (ja) * 1987-10-19 1995-04-12 富士写真フイルム株式会社 ハロゲン化銀写真感光材料
JPH0814682B2 (ja) * 1988-01-18 1996-02-14 富士写真フイルム株式会社 ハロゲン化銀感光材料
DE68925144T2 (de) * 1988-04-15 1996-06-13 Fuji Photo Film Co Ltd Lichtempfindliches photographisches Silberhalogenidmaterial
US5035986A (en) * 1989-01-30 1991-07-30 Fuji Photo Film Co., Ltd. Silver halide color photographic material
US5035992A (en) * 1989-11-30 1991-07-30 E. I. Du Pont De Nemours And Company Process for the stabilization of high-chloride crystals with modified crystal habit using bromide shells
WO1993010482A2 (fr) * 1991-11-12 1993-05-27 International Paper Company Emulsions et materiaux photographiques avec sensibilite reduite a la pression
EP0562476B1 (fr) 1992-03-19 2000-10-04 Fuji Photo Film Co., Ltd. Procédé pour la préparation d' une émulsion photographique à l' halogénure d' argent
US5525460A (en) 1992-03-19 1996-06-11 Fuji Photo Film Co., Ltd. Silver halide photographic emulsion and light-sensitive material using the same
JPH09152696A (ja) 1995-11-30 1997-06-10 Fuji Photo Film Co Ltd ハロゲン化銀カラー写真感光材料
US6746832B2 (en) * 2001-12-28 2004-06-08 Fuji Photo Film Co., Ltd. Color image forming method using silver halide color photosensitive material
CN106076371B (zh) * 2016-06-03 2019-05-10 通化师范学院 一种AgCl/Ag核壳结构纳米可见光催化剂的制备方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE636801A (fr) * 1962-09-01
GB1468286A (en) * 1973-09-03 1977-03-23 Du Pont Process for producing photographic silver halide emulsions
US4070190A (en) * 1973-09-03 1978-01-24 E. I. Du Pont De Nemours And Company Process for producing photographic silver halide emulsions having a core/shell structure
JPS5218311A (en) * 1975-08-01 1977-02-10 Fuji Photo Film Co Ltd Super high contrast silver halide photographic emulsion
US4335199A (en) * 1980-02-19 1982-06-15 E. I. Du Pont De Nemours And Company High contrast by imagewise iodide infection in a mixed silver halide system
JPS5779940A (en) * 1980-11-06 1982-05-19 Konishiroku Photo Ind Co Ltd Direct positive silver halide color photographic material
JPS5862652A (ja) * 1981-10-08 1983-04-14 Konishiroku Photo Ind Co Ltd 直接ポジカラ−画像の形成方法
JPS58108533A (ja) * 1981-12-02 1983-06-28 Konishiroku Photo Ind Co Ltd ハロゲン化銀カラ−写真感光材料
DE3229999A1 (de) * 1982-08-12 1984-02-16 Agfa-Gevaert Ag, 5090 Leverkusen Fotografische silberhalogenidemulsion

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JPS60222845A (ja) 1985-11-07
EP0154920A2 (fr) 1985-09-18
DE3409445A1 (de) 1985-09-19
EP0154920A3 (en) 1988-01-13
DE3567290D1 (en) 1989-02-09
US4605610A (en) 1986-08-12

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