EP0096726A1 - Emulsion d'halogenure d'argent et son procede de preparation - Google Patents

Emulsion d'halogenure d'argent et son procede de preparation Download PDF

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Publication number
EP0096726A1
EP0096726A1 EP83900061A EP83900061A EP0096726A1 EP 0096726 A1 EP0096726 A1 EP 0096726A1 EP 83900061 A EP83900061 A EP 83900061A EP 83900061 A EP83900061 A EP 83900061A EP 0096726 A1 EP0096726 A1 EP 0096726A1
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EP
European Patent Office
Prior art keywords
silver halide
emulsion
solvent
silver
grains
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.)
Withdrawn
Application number
EP83900061A
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German (de)
English (en)
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EP0096726A4 (fr
Inventor
Takeo Koitabashi
Toshifumi Iijima
Toshihiko Yagi
Yuji Hotta
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Konica Minolta Inc
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Konica Minolta Inc
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Publication date
Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc
Publication of EP0096726A1 publication Critical patent/EP0096726A1/fr
Publication of EP0096726A4 publication Critical patent/EP0096726A4/fr
Withdrawn legal-status Critical Current

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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
    • G03C1/005—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
    • G03C2001/0357—Monodisperse emulsion

Definitions

  • This invention relates to a light-sensitive silver halide emulsion for photography and more particularly to a light-sensitive silver halide emulsion of which the sensitivity, the antifogging property and the storability have been improved, and a method for preparing the same.
  • a monodispersed emulsion is advantageous not only for attainment of sensitization in a silver halide emulsion but also for an effective performance of high sensitivity with keeping a fogging property low in a step referred to as chemical sensitization which will be described in more detail below.
  • Silver halide emulsions prepared under such a condition as mentioned above comprise so called regular crystal grains which have any shape of cube, octahedron and tetradecahedron and have the face (100) and the face (111) at various proportions.
  • the present inventors prepared monodispersed emulsions comprising octahedral or tetradecahedral grains and conducted the generally known chemical sensitization thereon, however, they could merely obtain results equivalent or rather inferior indeed to those given by polydispersed emulsions generally used in the art.
  • octahedral grains have not heretofore been employed for nega type high sensitivity light-sensitive materials, although octahedral grains are assumed to have a good relationship between the antifogging property and the sensitivity according to Japanese Patent Publication No. 23443/1973, is that from view point of enchancement of sensitivity they have disadvantages in that a large amount of light-sensitive nuclei are produced through chemical sensitization and a large amount of silver ions are present between crystal lattices during exposure and hence they are inferior to grains having other shapes.
  • Such characteristics of octahedral grains can be understood from reports in Journal of Photographic Science 14; 181-184 (1966); ibid, 16: 102-113 (1968); Photographiche Korrespondenz, 106: 149-160 (1970) and Journal of Japanese Photographic Society, 42; 112-121 (1979). Further, since the progress of the chemical sensitization of tetradecahedral grains is expected to be dominated by the face (111), tetradecahedral grains are considered to exhibit the same characteristic as that of octahedral grains and actually our studies have revealed that tetradecahedral grains have a property similar to that of octahedral grains.
  • An object of the present invention is to provide a light-sensitive silver halide emulsion having a low fogging property and a high sensitivity.
  • Another object of the present invention is to provide a light-sensitive silver halide emulsion having an excellent storability.
  • Still another object of the present invention is to provide a method for preparing such a light-sensitive silver halide emulsion as described above.
  • a monodispersed silver halide emulsion comprising silver halide grains having a recess at the central part of the face (111) of octahedral crystals or tetradecahedral crystals; and a method for preparing a silver halide emulsion in which a monodispersed silver halide emulsion containing silver halide grains comprising octahedral crystals or tetradecahedral crystals is subjected, after formationof said silver halide grains, to treatment with a solvent for the silver halide to the degree that the recess is formed at the central part of the face (111) of crystals described above, followed by desalting.
  • a recess which is positioned at the central part of the case (111) of octahedral crystals or tetradecahedral crystals is a recess of which the depth is 0.20 Q to 0.05 Q at the deepest point thereof, wherein is a diameter of the circumsphere for the silver halide grain having said recess (octahedral or tetradecahedral crystals having such a recess are hereinafter referred to also as the "skeleton crystal of the present invention").
  • the silver halide emulsion according to the present invention includes emulsions in which a part or all of silver halide grain groups comprising octahedral or tetradecahedral crystals contained therein are grains having such a recess as described above, however, an emulsion in which 1 % or more (in terms of the number of grains) of said grain groups are grains having such a recess, and silver halide grain groups contained in said emulsion consist essentially of silver halide grains comprising octahedral crystals or tetradecahedral crystals is preferable, and also as to the degree to which the grains are subjected to treatment with a solvent for the silver halide (whereinafter referred to as "solvent treatment") in the manufacturing method of the present invention, such an emulsion as mentioned above is similarly preferable.
  • solvent treatment a solvent for the silver halide
  • the emulsion which has been subjected to the solvent treatment of the present invention has a lower fogging property and a higher sensitivity after chemical ripening as compared with an emulsion which has been subjected to solvent treatment so that the shapes of grainsbecome spherical forms, confetto-like forms (defined as such, when the depth of the recess as described above exceeds 0.20 l) or a potato-like forms (defined as such, when the outer crystal habit is indefinite and irregular, and the grains having the spherical form are indefinite also in the outer crystal habit but different from the potato-like form in the point that grain shapes are uniform).
  • the intensity of the diffracted ray for the face (220) is preferably less than 15 % of that for the face (111) and more preferably less than 8 %.
  • the monodispersed silver halide emulsion to be treated with a solvent may preferably such that the silver halide grains contained therein comprise essentially of octahedral or tetradecahedral silver halide crystals. Further, breadth of the grain size distribution of the silver halide grains contained in the monodispersed silver halide emulsion to be treated with a solvent is 15 % or less in terms of CV and more preferably 10 % or less.
  • solvent treatment may be conducted merely by adding a solvent for a silver halide (AgX) to a silver halide emulsion in which silver halide grains have been formed into the final size and shape through completion of a mixing or a mixing followed by a physical ripening procedure; and subsequently by mixing uniformly to act said solvent onto the surface of the silver halide grain. Therefore, there may be employed a procedure similar to a procedure for the conventional chemical ripening in which a solvent is used in place of a chemical sensitizer. Moreover, after formation of silver halide grains, there may be conducted desalting (including washing with water) prior to the solvent treatment.
  • desalting including washing with water
  • the solvent for a silver halide used in the manufacturing method of the present invention there may be employed any solvent capable of forming a recess at the central part of the face (111) of said grain surfaces when the solvent acts on the surface of said silver halide grains comprising octahedral or tetradecahedral crystals. Further, it is preferable that said solvent is not a compound capable of reacting with a silver halide to form silver sulfide.
  • Solvents for a silver halide employed in the present invention include (a) organic thioethers as described in U.S. Patent Nos. 3,271,157, 3,531,289 and 3,574,628, Japanese Provisional Patent Publication Nos. 1019/1979 and 158917/1979; (b) thiourea derivatives as described in Japanese Provisional Patent Publication Nos. 82408/1978, 77737/1980 and 2982/1980, (c) solvents for a silver halide having a thiocarbonyl group sandwiched between an oxygen atom or a sulfur atom and a nitrogen atom as discribed in Japanese Provisional Patent Publication No. 144319/1978 (d) imidazoles as described in Japanese Provisional Patent Publication No. 100717/1979, (e) sulfites, (f) thiocyanates and the like.
  • thiocyanates and sulfites.
  • Amount of the solvent used in the present invention may be, for example, in case of thiocyanate, preferably in the range of 0.5 to 5 g/mole AgX, though it is variable depending on the kind of a solvent and so on. In cases the amount is less than this range, substantial change in grain shape after solvent treatment is not observed, and in cases the amount exceeds this range, the progress of the physical ripening becomes remarkable and grain size distribution is liable to be broadened.
  • the radius of curvature of roundness at said vertex is less than 1/6 r, wherein r is a length of one side of a triangle supposedly formed by extending sides of an arbitrary triangle constituting the outer surface thereof; and for tetradecehedral crystals, when a polygon having the largest area selected from triangles, squares, hexagons and octagons which constitute the outer surface is noted, it is preferable that the radius of curvature of roundness at the vertex of said polygon is less than 1/6 r, wherein r is a length of one side of a polygon which is supposedly formed by extending sides thereof or r is a length of the longest side in case not a regular polygon.
  • n designates the number of measured grains and "ri” designates the grain size of a grain measured in order of i.
  • the effect of the method of the present invention is remarkably large as compared with the effect in case out of this range. It is inferred that this is attributable to the fact that the degree of the physical ripening becomes remarkable in case said difference is out of this range. If grain size distribution of the silver halide emulsion to be subjected to solvent treatment ranges within the value of CV described above, physical ripening is hard to occur and thereby the effect of the present invention can be sufficiently exhibited, with a result that the difference between grain size distributions before and after solvent treatment falls approximately within the range described above.
  • the silver halide emulsion of the present invention includes, as one of the embodiments, an emulsion comprising two or more kinds of the monodispersed emulsions according to the present invention having different average grain sizes in admixture with each other.
  • an emulsion comprising two or more kinds of the monodispersed emulsions according to the present invention having different average grain sizes in admixture with each other.
  • the grain groups containing the skelton crystals of the present invention or, the silver halide grain groups to be treated with a solvent comprise substantially grains which are octahedral crystals or tetradecahedral crystals and an effect given by grains having these crystal habits is unexpectedly large and remarkable as compared with that given by grains having other crystal habits than said habits.
  • tetradecahedral crystals constituted mainly of the face (111) (grains giving the external appearance of hexagon and square and grains giving the external appearance of square and triangle) is particularly preferable.
  • Tetradecahedral crystals constituted mainly of the face (100) is liable to become spherical when treated with a solvent.
  • the manufacturing method of the present invention is characterized in that after formation of silver halide grains, the grains are treated with a solvent for a silver halide to a specifically determined degree, before desalting and hence it is different from a technique in which a solvent for a silver halide, for example, ammonia is present at the time of formation of silver halide grains.
  • a monodispersed emulsion having silver halide grains comprising octahedral crystals or tetradecahedral crystals are preferably ones prepared according to the ammonia method.
  • This invention exhibits particularly large effect when it is applied to a silver halide emulsion for color development.
  • the sensitivity in an emulsion of the present invention reaches about six times the sensitivity given by an emulsion prepared without such solvent treatment of the present invention and further increase in fogging is scarecely observed even at such a high sensitivity.
  • Silver halide grains according to the present invention may coexist with a cadmium salt, a zinc salt, a lead salt, a thallium salt, a iridium salt or complex salts thereof, a rhodium salt or a complex salt thereof, or an ion complex salt and the like in the course of formation of grains, treatment with a solvent and so on.
  • silver halide emulsion there may be used, for example, silver bromide, silver iodide, silver chloride, silver chlorobromide, silver bromoiodide, silver chlorobromoiodide and the like.
  • the preferred silver halide emulsion comprises silver halobromide containing at least 50 mole % of silver bromide and the most preferred emulsion comprises silver iodobromide, particularly containing 10 mole % or less of silver iodide.
  • Silver halide grains of the present invention may be different in phases between inner portion and surface layer thereof or may comprise a uniform phase. Regardless of the distribution in composition of halogen within silver halide grains described above, reduction sensitization may be conducted at any stage before completion of grain growth and treatment with a solvent.
  • Silver halide grains according to the present invention have preferably an average grain size of 0.1 - 4 um and more preferably of 0.2 - 2 um.
  • the method for preparing the emulsion of the present invention there may be suitably employed, as means for desalting, the Nudel rinsing, dialysis or a coagulation technique, which is commonly employed in a general emulsion manufacture.
  • chemical ripening may be conducted by use in single or in combination of chemical sensitizers such as noble metal sensitizers, including water-solbule gold salts, water-soluble platinum salts, water-soluble palladium salts, water-soluble rhodium salts, water-soluble iridium salts and the like; a sulfur sensitizer; a selenium sensitizer; and reduction sensitizers including polyamine, stannous chloride and the like.
  • chemical sensitizers such as noble metal sensitizers, including water-solbule gold salts, water-soluble platinum salts, water-soluble palladium salts, water-soluble rhodium salts, water-soluble iridium salts and the like
  • sulfur sensitizer a selenium sensitizer
  • reduction sensitizers including polyamine, stannous chloride and the like.
  • the silver halide emulsion of the present invention can optically be sensitized to a desired wave length region.
  • a spectral sensitization method for the emulsion of the present invention is not particularly critical and can be accomplished, for example, by use in single or in combination (e.g., supersensitization) of spectral sensitizers such as cyanine dyes or merocyanine dyes including a zeromethine dye, a monomethine dye, a dimethine dye, a trimethine dye and the like.
  • the monodispersed silver halide emulsion of the present invention may be put to use keeping its grain size distribution intact or may be put to use in combination with two or more monodispersed emulsions having different average grain sizes by blending these emulsions at an arbitrary stage so as to obtain a disired gradation.
  • the emulsion of the present invention may include an emulsion containing silver halide grains other than those of the present invention to such an extent that the effectiveness of the present invention is not thereby impaired.
  • the emulsion of the present invention may include generally usable various additives depending on the purpose thereof.
  • additives described above there are mentioned, for example, stabilizers and antifogging agents such as azaindenes, triazoles, tetrazoles, imidazolium salts, tetrazolium salts, polyhydroxy compounds and the like; hardener such as aldehyde series, aziridine series, isoxazole series, vinylsulfonic series, acryloyl series, carbodiimide series, maleimide series, methanesulfonic ester series, triazine series and the like; development accelerators such as benzyl alcohol, polyoxyethylene series compounds and the like; image stabilizers such as chroman series, coumaran series, bisphenol series and phosphorous ester series; lubricants such as waxes, glycerides of higher fatty acids, higher esters of higher fatty acids and the like.
  • a coating agent improvers for permeability of a treatment solution, defoaming agents and agents for controlling various physical properties of light-sensitive materials
  • a various type of surfactants such as those of anionic type, cationic type, nonionic type or amphoteric type.
  • antistatic agents diacetylcellulose, styrene perfluoroalkyllithium maleate copolymer, an alkali salt of a reaction product between styrene maleic anhydride copolymer and p-aminobenzenesulfonic acid and the like are effective.
  • matting agents there may be mentioned methyl polymethacrylate, polystyrene, alkali-soluble polymers and the like.
  • colloidal silica As latexes which are added to improve the physical properties of the coated film, there may be mentioned acrylic esters, vinyl esters and the like and their copolymers with the other monomers having an ethylic group. As gelatin plasticizers there may be mentioned glycerin and glycol series compounds, and as thickening agents there may be mentioned styrene-sodium maleate copolymer, alkyl vinyl ether maleate copolymer and the like.
  • supports for the light-sensitive material manufactured by the use of the emulsion of the present invention which is prepared in the above-mentioned manner there may be mentioned, for example, baryta paper, polyethylene-coated paper, polypropylene synthetic paper, glass paper, cellulose acetate, cellulose nitrate, polyvinyl acetal, polypropylene, a polyester film, for example, poly- ethyleneterephthalate and the like, polystyrene and so on.
  • the support is suitably selected from them depending upon the use and the purpose of the silver halide light-sensitive photographic material, respectively.
  • Supports may be provided with undercoating if desired.
  • the emulsion of the present invention may be effectively used for a variety of light-sensitive materials for general black and white photography, X-ray photography, color photography, infrared photography, microphotography, silver dye bleach process, reversal development, diffusion transfer process and the like.
  • cyan, magenta and yellow couplers in a combination into the emulsion of the present invention which has previously been adjusted for red-sensitivity, green-sensitivity and blue-sensitivity.
  • yellow couplers there may be used open-chain ketomethylene series couplers known to the art, among which benzoylacetanilide series and pivaloylacetanilide series compounds are useful.
  • magenta couplers there may be used pyrazolone series compounds, indazolone series compounds and cyanoacetyl compounds and as cyan couplers, phenol series compounds, naphthol series compounds and the like.
  • the light-sensitive material prepared by the use of the emulsion of the present invention may be developed by a known method commonly used after exposure.
  • the black and white developer is an alkaline solution containing developing agents such as hydroxy benzenes, aminophenols, or aminobenzenes, and it may further contain alkali metal salts such as a sulfite, a carbonate, a bisulfite, a bromide and an iodide.
  • developing agents such as hydroxy benzenes, aminophenols, or aminobenzenes
  • alkali metal salts such as a sulfite, a carbonate, a bisulfite, a bromide and an iodide.
  • the light-sensitive material is for color photography, it may be developed by a color developing process which is commonly used. In a reversal process, it is firstly developed by a developer for a black and white negative and then subjected to white color exposure, or subjected to treatment in a bath containing an antifogging agent, and further developed for color development in an alkaline developing solution containing color developing agents.
  • any method may be applied.
  • the obtained emulsion was divided to each of which, ammonium rhodanide or tetramethylthiourea was added to conduct ripening at 50 °C, followed by desalting and washing with water according to the ordinary method and then pAg value was adjusted to 8.2 at 40 °C.
  • Table 1 added amounts of ammonium rhodanide and tetramethylthiourea and results with respect to grain shapes after treatment obtained by observation through an electron microscope. These emulsions were designated as Em - 1 to Em - 5.
  • Em - 1 is an emulsion for comparison, which has not been subjected to treatment.
  • 0.45 ml of a 0.2 % by weight aqueous solution of chloroauric acid tetrahydrate and 1.5 ml of a 0.25 % by weight aqueous solution of sodium thiosulfate dihydrate based on one mole of AgX were added and subjected to chemical ripening at 46 °C. After completion of the ripening, to these emulsions 4-hydroxy-6-methyl-1,3,3a,7-tetrazaindene and phenyl- mercaptotetra-zole were added.
  • Em - 1 to Em - 5 in Example 1 0.45 ml of a 0.2 % by weight aqueous chloroauric acid tetrahydrate solution and 1.5 ml of a 0.25 % by weight aqueous sodium thiosulfate dihydrate solution based on one mole of AgX were added respectively and the thus obtained emulsions were subjected to chemical ripening at 46 °C for 110, 60, 50, 30 and 30 minutes, respectively and divided into three portions.
  • spectral sensitizing dyes (1) to (3) as shown below were added in a amount so as to be 150 mg based on one mole of AgX in the form of a methanolic solution and stirred for 10 minutes.
  • emulsion No. period of time for chemical ripening and a kind of sensitizing dye corresponding to each samples.
  • Sample Nos. 12, 13, 15, 16, 18, 19, 21, 22, 24 and 25 were, however, exposed through a glass filter Y-48 (manufactured by Toshiba Glass Co., Ltd.). Results in sensitometry are shown in Table 6. As apparent from Table 6, the effectiveness of the present invention could be also recognized in case where a spectral sensitizing dye was added.
  • an emulsion having the same value of latitude as in the thus obtained emulsion was prepared according to the following method.
  • two kinds of monodispersed octahedral series silver iodobromide emulsions Em - 7 and Em - 8, which have an average grain size of 1.0 ⁇ m and 0.5 pm, respectively, and contain 2 mole % of silver iodide and the resultant emulsions were subjected to solvent treatment with 600 mg/ mole AgX of ammonium rhodanide at 50 °C for 60 minutes, followed by washing with water and then further subjected to the optimum sensitization with chloroauric acid and sodium thiosulfate, respectively.
  • Em - 7 : Em - 8 7 : 3 in terms of the ratio between weights of silver halide in Em - 7 and Em - 8, additives were added in the same manner as discribed in Example 1, and the mixture was coated to obtain Sample No. 28.
  • Sample Nos. 27 and 28 observation of silver halide grains in Sample Nos. 27 and 28 by the use of an electron microscopic photography revealed that Sample No. 27 has potato-shaped grains and Sample No. 28 has octahedral grains containing 1 % of skeleton crystals of the present invention.
  • Table 8 an emulsion prepared by blending monodispersed emulsions according to the present invention was superior to a polydispersed emulsion treated with a solvent, in the antifogging property and the sensitivity.
  • a monodispersed tetradecahedral series emulsion (giving appearances of hexagon and square) which comprises silver iodobromide containing 2 mole% of silver iodide and has an average grain size of 0.70 pm and a grain size distribution s of 8 % was prepared.
  • This emulsion was divided and to each emulsion ammonium rhodanide or tetramethylthiourea was added and the resultant emulsions were subjected to ripening at 50 °c for 60 minutes and adjusted to pAg 8.2 at 40 °C after desalting and washing with water according to the ordinary method. These emulsions were designated as Em - 9 to Em - 12.
  • Added amounts of ammonium rhodanide and tetramethylthiourea and results of observation on grain shapes after solvent treatment obtained through an electron microscope are shown in Table 9.
  • the silver halide emulsion according to the present invention exhibits a remarkably higher sensitivity as compared with an emulsion having ordinary tetradecahedral crystal grains, though only a slight change in grain shapes was observed, and further is able to reach a higher level of sensitivity and gives a mild increase in fogging generated by chemical ripening as compared with Em - 11 in which crystals are formed into approximately shperical shapes by solvent treatment with increased amount of solvent and Em - 12 comprising perfectly spherical grains, and thereby the degree of progressive for fogging was decreased.
  • Emulsions thus obtained were designated as Em - 13 to Em - 16.
  • Table 12 are shown added amounts of solvents and result of observation on grain shapes after treatment obtained through an electron microscope.
  • 0.3 ml of a 0.2 % by weight aqueous chloroauric acid tetrahydrate solution and 10.8 ml of a 0.25 % by weight aqueous sodium thiosulfate dihydrate solution based on 1 mole AgX were added and the resultant emulsions were subjected to chemical ripening at 51 ° C . Thereafter, addition of additives, coating, drying, development and sensitometry were conducted in the same manner as in Example 1. Samples thus obtained were designated as Sample Nos. 37 to 44. There are shown particulars of samples in Table 13 and results obtained by sensitometry in Table 14.

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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)

Abstract

Emulsion d'halogénure d'argent pour une utilisation photographique et son procédé de préparation. Une émulsion d'halogénure d'argent mono-dispersée contenant des grains d'halogénure d'argent de cristaux en forme d'octahèdre ou de tétradécahèdre et possédant un renfoncement dans le centre de la face (1 1 1) est sujette à un ternissement réduit et présente une sensibilité élevée. Cette émulsion est préparée en traitant une émulsion d'halogénure d'argent mono-dispersée contenant des grains d'halogénure d'argent de cristaux en forme d'octahèdre ou de tétradécahèdre avec un solvant pour l'halogénure d'argent.
EP19830900061 1981-12-19 1982-12-20 Emulsion d'halogenure d'argent et son procede de preparation. Withdrawn EP0096726A4 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP20552281A JPS58106532A (ja) 1981-12-19 1981-12-19 ハロゲン化銀乳剤およびその製造方法
JP205522/81 1981-12-19

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EP0096726A1 true EP0096726A1 (fr) 1983-12-28
EP0096726A4 EP0096726A4 (fr) 1984-08-08

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EP19830900061 Withdrawn EP0096726A4 (fr) 1981-12-19 1982-12-20 Emulsion d'halogenure d'argent et son procede de preparation.

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JP (1) JPS58106532A (fr)
WO (1) WO1983002173A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3737962A1 (de) * 1987-11-07 1989-05-18 Agfa Gevaert Ag Fotografisches material
US5385818A (en) * 1994-02-25 1995-01-31 Eastman Kodak Company Process for the preparation of silver halide emulsions and photographic elements containing hollow silver halide grains

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6080840A (ja) * 1983-10-07 1985-05-08 Fuji Photo Film Co Ltd ハロゲン化銀写真感光材料
JPS6175337A (ja) * 1984-09-20 1986-04-17 Konishiroku Photo Ind Co Ltd ハロゲン化銀乳剤の製造方法
JPH0820690B2 (ja) * 1986-02-03 1996-03-04 コニカ株式会社 ハロゲン化銀粒子及び核ハロゲン化銀粒子を含む写真感光材料
JPH0513943Y2 (fr) * 1986-04-01 1993-04-14
JP2529853B2 (ja) * 1987-06-12 1996-09-04 富士写真フイルム株式会社 ハロゲン化銀写真乳剤の製造方法
EP0300258B1 (fr) * 1987-07-24 1993-10-20 Minnesota Mining And Manufacturing Company Eléments photographiques comprenant des émulsions sensibles à la lumière au bromoiodure d'argent
DE69328884T2 (de) 1992-03-19 2000-12-07 Fuji Photo Film Co Ltd Verfahren zur Herstellung einer photographischen Silberhalogenidemulsion
DE69329509T2 (de) 1992-03-19 2001-05-03 Fuji Photo Film Co Ltd Verfahren zur Herstellung einer photographischen Silberhalogenidemulsion
JP2777949B2 (ja) 1992-04-03 1998-07-23 富士写真フイルム株式会社 ハロゲン化銀カラー写真感光材料
US5541053A (en) * 1993-10-20 1996-07-30 Eastman Kodak Company Process for the preparation of silver halide photographic emulsions containing grains having (100) faces with cavities and photographic emulsions so prepared
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

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Publication number Priority date Publication date Assignee Title
FR2114030A5 (fr) * 1970-11-13 1972-06-30 Kodak Pathe
FR2354574A1 (fr) * 1976-06-10 1978-01-06 Ciba Geigy Ag Procede de fabrication d'emulsions photographiques d'halogenure d'argent contenant des cristaux d'halogenure d'argent du type macle

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Publication number Priority date Publication date Assignee Title
DE2306447C2 (de) * 1973-02-09 1986-10-02 Agfa-Gevaert Ag, 5090 Leverkusen Fotografisches Aufzeichnungsmaterial
JPS57182730A (en) * 1981-05-06 1982-11-10 Konishiroku Photo Ind Co Ltd Photosensitive silver halide emulsion

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Publication number Priority date Publication date Assignee Title
FR2114030A5 (fr) * 1970-11-13 1972-06-30 Kodak Pathe
FR2354574A1 (fr) * 1976-06-10 1978-01-06 Ciba Geigy Ag Procede de fabrication d'emulsions photographiques d'halogenure d'argent contenant des cristaux d'halogenure d'argent du type macle

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* Cited by examiner, † Cited by third party
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3737962A1 (de) * 1987-11-07 1989-05-18 Agfa Gevaert Ag Fotografisches material
US5385818A (en) * 1994-02-25 1995-01-31 Eastman Kodak Company Process for the preparation of silver halide emulsions and photographic elements containing hollow silver halide grains

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WO1983002173A1 (fr) 1983-06-23
JPS58106532A (ja) 1983-06-24
EP0096726A4 (fr) 1984-08-08

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