EP0534395B2 - Hochchloridhaltige Emulsionen hoher Tafelförmigkeit von aussergewöhnlicher Stabilität - Google Patents

Hochchloridhaltige Emulsionen hoher Tafelförmigkeit von aussergewöhnlicher Stabilität Download PDF

Info

Publication number
EP0534395B2
EP0534395B2 EP92116262A EP92116262A EP0534395B2 EP 0534395 B2 EP0534395 B2 EP 0534395B2 EP 92116262 A EP92116262 A EP 92116262A EP 92116262 A EP92116262 A EP 92116262A EP 0534395 B2 EP0534395 B2 EP 0534395B2
Authority
EP
European Patent Office
Prior art keywords
grain
tabular grains
silver
tabular
chloride
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
EP92116262A
Other languages
English (en)
French (fr)
Other versions
EP0534395B1 (de
EP0534395A1 (de
Inventor
Thomas B. c/o EASTMAN KODAK COMPANY Brust
Gary L. c/o EASTMAN KODAK COMPANY House
Joe E. c/o EASTMAN KODAK COMPANY Maskasky
Debra L. c/o EASTMAN KODAK COMPANY Hartsell
Donald L. c/o EASTMAN KODAK COMPANY Black
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.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27117531&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0534395(B2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co
Publication of EP0534395A1 publication Critical patent/EP0534395A1/de
Publication of EP0534395B1 publication Critical patent/EP0534395B1/de
Application granted granted Critical
Publication of EP0534395B2 publication Critical patent/EP0534395B2/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

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
    • G03C1/0051—Tabular grain emulsions
    • G03C1/0053—Tabular grain emulsions with high content of silver chloride
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/04—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
    • G03C1/047—Proteins, e.g. gelatine derivatives; Hydrolysis or extraction products of proteins
    • 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
    • G03C1/07—Substances influencing grain growth during silver salt formation
    • 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
    • G03C1/08—Sensitivity-increasing substances
    • G03C1/10—Organic substances
    • G03C1/12—Methine and polymethine dyes
    • G03C1/14—Methine and polymethine dyes with an odd number of CH groups
    • G03C1/16—Methine and polymethine dyes with an odd number of CH groups with one CH group
    • 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
    • G03C1/08—Sensitivity-increasing substances
    • G03C1/10—Organic substances
    • G03C1/12—Methine and polymethine dyes
    • G03C1/14—Methine and polymethine dyes with an odd number of CH groups
    • G03C1/18—Methine and polymethine dyes with an odd number of CH groups with three CH groups
    • 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
    • G03C1/0051—Tabular grain emulsions
    • G03C2001/0055—Aspect ratio of tabular grains in general; High aspect ratio; Intermediate aspect ratio; Low aspect ratio
    • 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
    • G03C1/015—Apparatus or processes for the preparation of emulsions
    • G03C2001/0156—Apparatus or processes for the preparation of emulsions pAg value; pBr value; pCl value; pI value
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/035—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein characterised by the crystal form or composition, e.g. mixed grain
    • G03C2001/03511—Bromide content
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/035—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein characterised by the crystal form or composition, e.g. mixed grain
    • G03C2001/03558—Iodide content
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • 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
    • G03C2001/03594—Size of the grains
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C2200/00—Details
    • G03C2200/01—100 crystal face

Definitions

  • the invention relates to silver halide photography. More specifically, the invention relates to radiation sensitive silver halide emulsions useful in photography.
  • tabular grain emulsions To distinguish tabular grain emulsions from those that contain only incidental tabular grain inclusions it is also the recognized practice of the art to require that a significant percentage (e.g., greater than 30 percent and more typically greater than 50 percent) of total grain projected area be accounted for by tabular grains.
  • An emulsion is generally understood to be a "high aspect ratio tabular grain emulsion" when tabular grains having a thickness of less than 0.3 ⁇ m have an average aspect ratio of greater than 8 and account for greater than 50 percent of total grain projected area.
  • the difficulty in achieving high average aspect ratios in high chloride tabular grain emulsions has often led to accepting average aspect ratios of greater than 5 as the best available approximations of high average aspect ratios.
  • the term "thin tabular grain” is generally understood to be a tabular grain having a thickness of less than 0.2 ⁇ m.
  • the term “ultrathin tabular grain” is generally understood to be a tabular grain having a thickness of 0.06 ⁇ m or less. High chloride thin tabular grain emulsions have been difficult to prepare and ultrathin high chloride tabular grain emulsions have been completely unknown.
  • tabular grain emulsions satisfying grain thickness (t), average aspect ratio (ECD/t), average tabularity (ECD/t 2 ) and projected area aims have been formed by introducing two or more parallel twin planes into octahedral grains during their preparation.
  • Regular octahedral grains are bounded by ⁇ 111 ⁇ crystal faces.
  • the predominant feature of tabular grains formed by twinning are opposed parallel ⁇ 111 ⁇ major crystal faces.
  • the major crystal faces have a three fold symmetry, typically appearing triangular or hexagonal.
  • tabular grain emulsions containing parallel twin planes is most easily accomplished in the preparation of silver bromide emulsions.
  • the art has developed the capability of including photographically useful levels of iodide.
  • the inclusion of high levels of chloride as opposed to bromide, alone or in combination with iodide, has been difficult.
  • Silver chloride differs from silver bromide in exhibiting a much stronger propensity toward the formation of grains with faces lying in ⁇ 100 ⁇ crystographic planes. Unfortunately, twinning of grains bounded by ⁇ 100 ⁇ crystal faces does not produce grains having a tabular shape.
  • Maskasky U.S. Patent 4,400,463 developed a strategy for preparing a high chloride emulsion containing tabular grains with parallel twin planes and ⁇ 111 ⁇ major crystal faces with the significant advantage of tolerating significant internal inclusions of the other halides.
  • the strategy was to use a particularly selected synthetic polymeric peptizer in combination with a grain growth modifier having as its function to promote the formation of ⁇ 111 ⁇ crystal faces.
  • Adsorbed aminoazaindenes, preferably adenine, and iodide ions were disclosed to be useful grain growth modifiers.
  • Maskasky U.S. Patent 4,713,323 significantly advanced the state of the art by preparing high chloride emulsions containing tabular grains with parallel twin planes and ⁇ 111 ⁇ major crystal faces using an aminoazaindene growth modifier and a gelatino-peptizer containing up to 30 micromoles per gram of methionine. Since the methionine content of a gelatino-peptizer, if objectionably high, can be readily reduced by treatment with a strong oxidizing agent (or alkylating agent, King et al U.S. Patent 4,942,120), Maskasky II placed within reach of the art high chloride tabular grain emulsions with significant bromide and iodide ion inclusions prepared starting with conventional and universally available peptizers.
  • a strong oxidizing agent or alkylating agent, King et al U.S. Patent 4,942,120
  • Bogg U.S. Patent 4,063,951 reported the first emulsions to contain tabular grains having parallel ⁇ 100 ⁇ major crystal faces.
  • the tabular grains of Bogg exhibited square or rectangular major faces, thus lacking the three fold symmetry of conventional tabular grain ⁇ 111 ⁇ major crystal faces.
  • Bogg employed an ammoniacal ripening process for preparing the tabular grains, thereby encounter-ing the grain thickening and pH disadvantages discussed above in connection with Wey.
  • Bogg observed tabular grains having aspect ratios ranging from 1.5:1 to 7:1.
  • the tabular grains in the emulsion of Figure 3 of Bogg are stated to have an average aspect ratio of 2:1.
  • Mignot U.S. Patent 4,386,156 represents an improvement over Bogg in that the disadvantages of ammoniacal ripening were avoided in preparing a silver bromide emulsion containing tabular grains with square and rectangular major faces.
  • Mignot specifically requires ripening in the absence of silver halide ripening agents other than bromide ion (e.g., thiocyanate, thioether or ammonia).
  • Mignotrelies on excess bromide ion for ripening Since silver bromide exhibits a solubility approximately two orders of magnitude lower than that of silver chloride, reliance on excess bromide ion for ripening precludes the formation of high chloride tabular grains.
  • this invention is directed to a radiation sensitive emulsion containing a silver halide grain population comprised of at least 50 mole percent chloride, based on total silver forming the grain population, in which greater than 50 percent of the grain population projected area is accounted for by tabular grains having a mean thickness of less than 0.3 ⁇ m, and wherein the tabular grains have parallel major faces lying in ⁇ 100 ⁇ crystallographic planes.
  • tabular grains bounded by ⁇ 100 ⁇ major faces a portion accounting for 50 percent of total grain projected area selected on the criteria of adjacent major face edge ratios of less than 10 and thicknesses of less than 0.3 ⁇ m and having higher aspect ratios than any remaining tabular grains satisfying these criteria have an average aspect ratio of greater than 8.
  • this invention is directed to the process of claim 10.
  • the process is characterized in that of the tabular grains bounded by ⁇ 100 ⁇ major faces a portion accounting for 50 percent of total grain projected area selected on the criteria of adjacent major face edge ratios of less than 10 and thicknesses of less than 0.3 ⁇ m and having higher aspect ratios than any remaining tabular grains satisfying these criteria (1) have an average aspect ratio of greater than 8 and (2) internally at their nucleation site contain iodide and at least 50 mole percent chloride, at least the selected portion of the tabular grains being formed by nucleation in the presence of iodide with chloride accounting for at least 50 mole percent of the halide present in the dispersing medium and the pCl of the dispersing medium being maintained in the range of from 0.5 to 3.5.
  • the invention in one preferred form is based on the discovery of a novel approach to forming tabular grains. Instead of introducing parallel twin planes in grains as they are being formed to induce tabularity and thereby produce tabular grains with ⁇ 111 ⁇ major faces, it has been discovered that the presence of iodide in the dispersing medium during a high chloride nucleation step coupled with maintaining the chloride ion in solution within a selected pCl range results in the formation of a high aspect ratio tabular grain emulsion in which the tabular grains are bounded by ⁇ 100 ⁇ crystal faces.
  • the preferred form of the invention represent the discovery of a novel process for preparing tabular grain emulsions, the emulsions that are produced by the process are novel. Further, alternative processes of preparation are disclosed that do not require the presence of iodide during grain nucleation and hence render iodide incorporation within the high chloride tabular grains of the invention a matter of choice.
  • the invention places within the reach of the art tabular grains bounded by ⁇ 100 ⁇ crystal faces with halide contents, halide distributions and grain thicknesses that have not been heretofore realized.
  • the present invention provides the first ultrathin tabular grain emulsion in which the grains are bounded by ⁇ 100 ⁇ crystal faces.
  • the invention provides high aspect ratio tabular grain high chloride emulsions exhibiting high levels of grain stability. Unlike high chloride tabular grain emulsions in which the tabular grains have ⁇ 111 ⁇ major faces, the emulsions of the invention do not require a morphological stabilizer adsorbed to the major faces of the grains to maintain their tabular form. Finally, while clearly applicable to high chloride emulsions, the present invention extends beyond high chloride emulsions to those containing a wide range of bromide, iodide and chloride concentrations.
  • the invention is directed to a photographically useful, radiation sensitive emulsion containing a silver halide grain population comprised of at least 50 mole percent chloride, based on total silver forming the grain population, in which greater than 50 percent of the grain population projected area is accounted for by tabular grains tabular grains having a mean thickness of less than 0.3 ⁇ m.
  • the tabular grains have parallel major faces lying in ⁇ 100 ⁇ crystallographic planes.
  • tabular grains bounded by ⁇ 100 ⁇ major faces those accounting for 50 percent of the total grain projected area, selected on the criteria of (1) adjacent major face edge ratios of less than 10, (2) thicknesses of less than 0.3 ⁇ m and (3) higher aspect ratios than any remaining tabular grains satisfying criteria (1) and (2), have an average aspect ratio of greater than 8.
  • Figure 1 is a shadowed photomicrograph of carbon grain replicas of a representative emulsion of the invention, described in detail in Example 1 below. It is immediately apparent that most of the grains have orthogonal tetragonal (square or rectangular) faces. The orthogonal tetragonal shape of the grain faces indicates that they are ⁇ 100 ⁇ crystal faces.
  • rods acicular or rod-like grains
  • These grains are more than 10 times longer in one dimension than in any other dimension and can be excluded from the desired tabular grain population based on their high ratio of edge lengths.
  • the projected area accounted for by the rods is low, but, when rods are present, their projected area is noted for determining total grain projected area.
  • the grains remaining all have square or rectangular major faces, indicative of ⁇ 100 ⁇ crystal faces.
  • Some of these grains are regular cubic grains. That is, they are grains that have three mutually perpendicular edges of equal length. To distinguish cubic grains from tabular grains it is necessary to measure the grain shadow lengths. From a knowledge of the angle of illumination (the shadow angle) it is possible to calculate the thickness of a grain from a measurement of its shadow length. The projected areas of the cubic grains are included in determining total grain projected area.
  • Each of the grains having a square or rectangular face and a thickness of less than 0.3 ⁇ m is examined.
  • the projected area (the product of edge lengths) of the upper surface of each grain is noted. From the grain projected area the ECD of the grain is calculated.
  • the thickness (t) of the grain and its aspect ratio (ECD/t) of the grain are next calculated.
  • these grains are rank ordered according to aspect ratio.
  • the grain with the highest aspect ratio is rank ordered first and the grain with the lowest aspect ratio is rank ordered last.
  • the aspect ratios of the selected tabular grain population are then averaged.
  • the average aspect ratio of the selected tabular grain population is greater than 8.
  • average aspect ratios of the selected tabular grain population are greater than 12 and optimally at least 20.
  • the average aspect ratio of the selected tabular grain population ranges up to 50, but higher aspect ratios of 100, 200 or more can be realized.
  • the selected tabular grain population accounting for 50 percent of total grain projected area preferably exhibits major face edge length ratios of less than 5 and optimally less than 2.
  • the tabular grain population is selected on the basis of tabular grain thicknesses of less than 0.2 ⁇ m instead of 0.3 ⁇ m.
  • the emulsions are in this instance thin tabular grain emulsions.
  • ultrathin tabular grain emulsions have been prepared satisfying the requirements of the invention.
  • Ultrathin tabular grain emulsions are those in which the selected tabular grain population is made of up tabular grains having thicknesses of less than 0.06 ⁇ m.
  • the only ultrathin tabular grain emulsions of a halide content exhibiting a cubic crystal lattice structure known in the art contained tabular grains bounded by ⁇ 111 ⁇ major faces. In other words, it was thought essential to form tabular grains by the mechanism of parallel twin plane incorporation to achieve ultrathin dimensions.
  • Emulsions according to the invention can be prepared in which the selected tabular grain population has a mean thickness down to 0.02 ⁇ m and even 0.01 ⁇ m.
  • Ultrathin tabular grains have extremely high surface to volume ratios. This permits ultrathin grains to be photographically processed at accelerated rates. Further, when spectrally sensitized, ultrathin tabular grains exhibit very high ratios of speed in the spectral region of sensitization as compared to the spectral region of native sensitivity. For example, ultrathin tabular grain emulsions according to the invention can have entirely negligible levels of blue sensitivity, and are therefore capable of providing a green or red record in a photographic product that exhibits minimal blue contamination even when located to receive blue light.
  • the selected tabular grain population can exhibit an average ECD of any photographically useful magnitude compatible with a tabularity of greater than 25.
  • ECD's for photographic utility average ECD's of less than 10 ⁇ m are contemplated, although average ECD's in most photographic applications rarely exceed 6 ⁇ m.
  • a minimum ECD to satisfy minimum tabularity requirements with a minimum grain thickness of the selected tabular grain population is just greater than 0.25 ⁇ m.
  • emulsions with selected tabular grain populations having higher ECD's are advantageous for achieving relatively high levels of photographic sensitivity while selected tabular grain populations with lower ECD's are advantageous in achieving low levels of granularity.
  • the advantageous properties of the emulsions of the invention are increased as the proportion of tabular grains having thicknesses of less than 0.3 ⁇ m and ⁇ 100 ⁇ major faces is increased.
  • the emulsions according to the invention are those in which at least 50 percent, most preferably at least 70 percent and optimally at least 90 percent of total grain projected area is accounted for by tabular grains having ⁇ 100 ⁇ major faces. It is specifically contemplated to provide emulsions satisfying the grain descriptions above in which the selection of the rank ordered tabular grains extends to sufficient tabular grains to account for 70 percent or even 90 percent of total grain projected area.
  • the emulsion does not satisfy the requirements of the invention and isa photographically inferior emulsion.
  • emulsions are photographically inferior in which many or all of the tabular grains are relatively thick--e.g., emulsions containing high proportions of tabular grains with thicknesses in excess of 0.3 ⁇ m.
  • inferior emulsions failing to satisfy the requirements of the invention have an excessive proportion of total grain projected area accounted for by cubes, twinned nontabular grains, and rods. Such an emulsion is shown in Figure 2. Most of the grain projected area is accounted for by cubic grains. Also the rod population is much more pronounced than in Figure 1. A few tabular grains are present, but they account for only a minor portion of total grain projected area.
  • the tabular grain emulsion of Figure 1 satisfying the requirements of the invention and the predominantly cubic grain emulsion of Figure 2 were prepared under conditions that were identical, except for iodide management during nucleation.
  • the Figure 2 emulsion is a silver chloride emulsion while the emulsion of Figure 1 additionally includes a small amount of iodide.
  • emulsions satisfying the requirements of the invention has been achieved by the discovery of a novel precipitation process.
  • grain nucleation occurs in a high chloride environment in the presence of iodide ion under conditions that favor the emergence of ⁇ 100 ⁇ crystal faces.
  • iodide ion the inclusion of iodide into the cubic crystal lattice being formed by silver ions and the remaining halide ions is disruptive because of the much larger diameter of iodide ion as compared to chloride ion.
  • the incorporated iodide ions introduce crystal irregularities that in the course of further grain growth result in tabular grains rather than regular (cubic) grains.
  • cubic grain nuclei being formed having one or more screw dislocations in one or more of the cubic crystal faces.
  • the cubic crystal faces that contain at least one screw dislocation thereafter accept silver halide at an accelerated rate as compared to the regular cubic crystal faces (i.e., those lacking a screw dislocation).
  • the regular cubic crystal faces i.e., those lacking a screw dislocation.
  • any two contiguous cubic crystal faces contain a screw dislocation
  • continued growth accelerates growth on both faces and produces a tabular grain structure.
  • the tabular grains of the emulsions of this invention are produced by those grain nuclei having two, three or four faces containing screw dislocations.
  • a reaction vessel containing a dispersing medium and conventional silver and reference electrodes for monitoring halide ion concentrations within the dispersing medium.
  • Halide ion is introduced into the dispersing medium that is at least 50 mole percent chloride--i.e., at least half by number of the halide ions in the dispersing medium are chloride ions.
  • the pCl of the dispersing medium is adjusted to favor the formation of ⁇ 100 ⁇ grain faces on nucleation--that is, within the range of from 0.5 to 3.5, preferably within the range of from 1.0 to 3.0 and, optimally, within the range of from 1.5 to 2.5.
  • the grain nucleation step is initiated when a silver jet is opened to introduce silver ion into the dispersing medium.
  • Iodide ion is preferably introduced into the dispersing medium concurrently with or, optimally, before opening the silver jet.
  • Effective tabular grain formation can occur over a wide range of iodide ion concentrations ranging up to the saturation limit of iodide in silver chloride.
  • the saturation limit of iodide in silver chloride is reported by H. Hirsch, "Photographic Emulsion Grains with Cores: Part I. Evidence for the Presence of Cores", J. of Photog. Science, Vol. 10 (1962), pp. 129-134, to be 13 mole percent.
  • iodide grains in which equal molar proportions of chloride and bromide ion are present up to 27 mole percent iodide, based on silver, can be incorporated in the grains. It is preferred to undertake grain nucleation and growth below the iodide saturation limit to avoid the precipitation of a separate silver iodide phase and thereby avoid creating an additional category of unwanted grains. It is generally preferred to maintain the iodide ion concentration in the dispersing medium at the outset of nucleation at less than 10 mole percent. In fact, only minute amounts of iodide at nucleation are required to achieve the desired tabular grain population. Initial iodide ion concentrations of down to 0.001 mole percent are contemplated. However, for convenience in replication of results, it is preferred to maintain initial iodide concentrations of at least 0.01 mole percent and, optimally, at least 0.05 mole percent.
  • silver iodochloride grain nuclei are formed during the nucleation step. Minor amounts of bromide ion can be present in the dispersing medium during nucleation. Any amount of bromide ion can be present in the dispersing medium during nucleation that is compatible with at least 50 mole percent of the halide in the grain nuclei being chloride ions.
  • the grain nuclei preferably contain at least 70 mole percent and optimally at least 90 mole percent chloride ion, based on silver.
  • Grain nuclei formation occurs instantaneously upon introducing silver ion into the dispersing medium.
  • silver ion introduction during the nucleation step is preferably extended for a convenient period, typically from 5 seconds to less than a minute. So long as the pCl remains within the ranges set forth above no additional chloride ion need be added to the dispersing medium during the nucleation step. It is, however, preferred to introduce both silver and halide salts concurrently during the nucleation step.
  • the advantage of adding halide salts concurrently with silver salt throughout the nucleation step is that this permits assurance that any grain nuclei formed after the outset of silver ion addition are of essentially similar halide content as those grain nuclei initially formed.
  • Iodide ion addition during the nucleation step is particularly preferred. Since the deposition rate of iodide ion far exceeds that of the other halides, iodide will be depleted from the dispersing medium unless replenished.
  • Silver ion is preferably introduced as an aqueous silver salt solution, such as a silver nitrate solution.
  • Halide ion is preferably introduced as alkali or alkaline earth halide, such as lithium, sodium and/or potassium chloride, bromide and/or iodide.
  • the dispersing medium contained in the reaction vessel prior to the nucleation step is comprised of water, the dissolved halide ions discussed above and a peptizer.
  • the dispersing medium can exhibit a pH within any convenient conventional range for silver halide precipitation, typically from 2 to 8. It is preferred, but not required, to maintain the pH of the dispersing medium on the acid side of neutrality, preferably in a pH range of from 5,0 to 7.0.
  • Mineral acids such as nitric acid or hydrochloride acid
  • bases such as alkali hydroxides
  • the peptizer can take any convenient conventional form known to be useful in the precipitation of photographic silver halide emulsions and particularly tabular grain silver halide emulsions.
  • a summary of conventional peptizers is provided in Research Disclosure , Vol. 308, December 1989, Item 308119, Section IX, the disclosure of which is here incorporated by reference. Research Disclosure is published by Kenneth Mason Publications, Ltd., Emsworth, Hampshire P010 7DD, England. While synthetic polymeric peptizers of the type disclosed by Maskasky I, cited above and here incorporated by reference, can be employed, it is preferred to employ gelatino peptizers (e.g., gelatin and gelatin derivatives).
  • gelatino peptizers e.g., gelatin and gelatin derivatives.
  • peptizers are low methionine gelatino peptizers (i.e., those containing less than 30 micromoles of methionine per gram of peptizer), optimally less than 12 micromoles of methionine per gram of peptizer, these peptizers and their preparation are described by Maskasky II and King et al, cited above, the disclosures of which are here incorporated by reference.
  • the grain growth modifiers of the type taught for inclusion in the emulsions of Maskasky I and II are not appropriate for inclusion in the dispersing media of this invention, since these grain growth modifiers promote twinning and the formation of tabular grains having ⁇ 111 ⁇ major faces.
  • adenine e.g., adenine
  • the grain growth modifiers promote twinning and the formation of tabular grains having ⁇ 111 ⁇ major faces.
  • at least about 10 percent and typically from 20 to 80 percent of the dispersing medium forming the completed emulsion is present in the reaction vessel at the outset of the nucleation step. It is conventional practice to maintain relatively low levels of peptizer, typically from 10 to 20 percent of the peptizer present in the completed emulsion, in the reaction vessel at the start of precipitation.
  • the concentration of the peptizer in the dispersing medium be in the range of from 0.5 to 6 percent by weight of the total weight of the dispersing medium at the outset of the nucleation step. It is conventional practice to add gelatin, gelatin derivatives and other vehicles and vehicle extenders to prepare emulsions for coating after precipitation. Any naturally occurring level of methionine can be present in gelatin and gelatin derivatives added after precipitation is complete.
  • the nucleation step can be performed at any convenient conventional temperature for the precipitation of silver halide emulsions. Temperatures ranging from near ambient--e.g., 30°C up to about 90°C are contemplated, with nucleation temperatures in the range of from 35 to 70°C being preferred.
  • a grain growth step follows the nucleation step in which the grain nuclei are grown until tabular grains having ⁇ 100 ⁇ major faces of a desired average ECD are obtained.
  • the objective of the nucleation step is to form a grain population having the desired incorporated crystal structure irregularities
  • the objective of the growth step is to deposit additional silver halide onto (grow) the existing grain population while avoiding or minimizing the formation of additional grains. If additional grains are formed during the growth step, the polydispersity of the emulsion is increased and, unless conditions in the reaction vessel are maintained as described above for the nucleation step, the additional grain population formed in the growth step will not have the desired tabular grain properties described above.
  • the process of preparing emulsions according to the invention can be performed as a single jet precipitation without interrupting silver ion introduction from start to finish.
  • a spontaneous transition from grain formation to grain growth occurs even with an invariant rate of silver ion introduction, since the increasing size of the grain nuclei increases the rate at which they can accept silver and halide ion from the dispersing medium until a point is reached at which they are accepting silver and halide ions at a sufficiently rapid rate that no new grains can form.
  • single jet precipitation limits halide content and profiles and generally results in more polydisperse grain populations.
  • emulsions In the preparation of emulsions according to the invention it is preferred to interrupt silver and halide salt introductions at the conclusion of the nucleation step and before proceeding to the growth step that brings the emulsions to their desired final size and shape.
  • the emulsions are held within the temperature ranges described above for nucleation for a period sufficient to allow reduction in grain dispersity.
  • a holding period can range from a minute to several hours, with typical holding periods ranging from 5 minutes to an hour.
  • relatively smaller grain nuclei are Ostwald ripened onto surviving, relatively larger grain nuclei, and the overall result is a reduction in grain dispersity.
  • the rate of ripening can be increased by the presence of a ripening agent in the emulsion during the holding period.
  • a conventional simple approach to accelerating ripening is to increase the halide ion concentration in the dispersing medium. This creates complexes of silver ions with plural halide ions that accelerate ripening. When this approach is employed, it is preferred to increase the chloride ion concentration in the dispersing medium. That is, it is preferred to lower the pCl of the dispersing medium into a range in which increased silver chloride solubility is observed.
  • ripening can be accelerated by employing conventional ripening agents.
  • Preferred ripening agents are sulfur containing ripening agents, such as thioethers and thiocyanates.
  • Typical thiocyanate ripening agents are disclosed by Nietz et al U.S. Patent 2,222,264, Lowe et al U.S. Patent 2,448,534 and Illingsworth U.S. Patent 3,320,069, the disclosures of which are here incorporated by reference.
  • Typical thiocyanate ripening agents are disclosed by McBride U.S. Patent 3,271,157, Jones U.S. Patent 3,574,628 and Rosencrantz et al U.S. Patent 3,737,313, the disclosures of which are here incorporated by reference. More recently crown thioethers have been suggested for use as ripening agents.
  • grain growth to obtain the emulsions of the invention can proceed according to any convenient conventional precipitation technique for the precipitation of silver halide grains bounded by ⁇ 100 ⁇ grain faces.
  • any halide or combination of halides known to form a cubic crystal lattice structure can be employed during the growth step.
  • iodide nor chloride ions need be incorporated in the grains during the growth step, since the irregular grain nuclei faces that result in tabular grain growth, once introduced, persist during subsequent grain growth independently of the halide being precipitated, provided the halide or halide combination is one that forms a cubic crystal lattice.
  • silver bromide or silver iodobromide When silver bromide or silver iodobromide is being deposited during the growth step, it is preferred to maintain a pBr within the dispersing medium in the range of from 1.0 to 4.2, preferably 1.6 to 3.4.
  • a pBr When silver chloride, silver iodochloride, silver bromochloride or silver iodobromochloride is being deposited during the growth step, it is preferred to maintain the pCl within the dispersing medium within the ranges noted above in describing the nucleation step.
  • both silver and halide salts are preferably introduced into the dispersing medium.
  • double jet precipitation is contemplated, with added iodide salt, if any, being introduced with the remaining halide salt or through an independent jet.
  • the rate at which silver and halide salts are introduced is controlled to avoid renucleation--that is, the formation of a new grain population. Addition rate control to avoid renucleation is generally well known in the art, as illustrated by Wilgus German OLS No. 2,107,118, Irie U.S. Patent 3,650,757, Kurz U.S. Patent 3,672,900, Saito U.S.
  • peptizers that exhibit reduced adhesion to grain surfaces.
  • low methionine gelatin of the type disclosed by Maskasky II is less tightly absorbed to grain surfaces than gelatin containing higher levels of methionine.
  • Further moderated levels of grain adsorption can be achieved with so-called “synthetic peptizers"--that is, peptizers formed from synthetic polymers.
  • the maximum quantity of peptizer compatible with limited coalescence of grain nuclei is, of course, related to the strength of adsorption to the grain surfaces.
  • the emulsions of the invention include silver chloride, silver bromochloride, silver iodochloride, silver iodobromochloride and silver bromoiodochloride emulsions, where halides are named in order of increasing concentrations.
  • the invention is advantageous in providing high chloride (greater than 50 mole percent chloride) tabular grain emulsions, since conventional high chloride tabular grain emulsions having tabular grains bounded by ⁇ 111 ⁇ are inherently unstable and require the presence of a morphological stabilizer to prevent the grains from regressing to nontabular forms.
  • Particularly preferred high chloride emulsions are according to the invention that are those that contain more than 70 mole percent (optimally more than 90 mole percent) chloride.
  • a further procedure that can be employed to maximize the population of tabular grains having ⁇ 100 ⁇ major faces is to incorporate an agent capable of restraining the emergence of non- ⁇ 100 ⁇ grain crystal faces in the emulsion during its preparation.
  • the restraining agent when employed, can be active during grain nucleation, during grain growth or throughout precipitation.
  • Useful restraining agents under the contemplated conditions of precipitation are organic compounds containing a nitrogen atom with a resonance stabilized ⁇ electron pair. Resonance stabilization prevents protonation of the nitrogen atom under the relatively acid conditions of precipitation.
  • Aromatic resonance can be relied upon for stabilization of the ⁇ electron pair of the nitrogen atom.
  • the nitrogen atom can either be incorporated in an aromatic ring, such as an azole or azine ring, or the nitrogen atom can be a ring substituent of an aromatic ring.
  • the restraining agent can satisfy the following formula: where Z represents the atoms necessary to complete a five or six membered aromatic ring structure, preferably formed by carbon and nitrogen ring atoms.
  • Preferred aromatic rings are those that contain one, two or three nitrogen atoms.
  • Specifically contemplated ring structures include 2H-pyrrole, pyrrole, imidazole, pyrazole, 1,2,3-triazole, 1,2,4-triazole, 1,3,5-triazole, pyridine, pyrazine, pyrimidine, and pyridazine.
  • Ar is an aromatic ring structure containing from 5 to 14 carbon atoms and R 1 and R 2 are independently hydrogen, Ar, or any convenient aliphatic group or together complete a five or six membered ring.
  • Ar is preferably a carbocyclic aromatic ring, such as phenyl or naphthyl.
  • any of the nitrogen and carbon containing aromatic rings noted above can be attached to the nitrogen atom of formula II through a ring carbon atom. In this instance, the resulting compound satisfies both formulae I and II. Any of a wide variety of aliphatic groups can be selected.
  • the simplest contemplated aliphatic groups are alkyl groups, preferably those containing from 1 to 10 carbon atoms and most preferably from 1 to 6 carbon atoms. Any functional substituent of the alkyl group known to be compatible with silver halide precipitation can be present. It is also contemplated to employ cyclic aliphatic substituents exhibiting 5 or 6 membered rings, such as cycloalkane, cycloalkene and aliphatic heterocyclic rings, such as those containing oxygen and/or nitrogen hetero atoms. Cyclopentyl, cyclohexyl, pyrrolidinyl, piperidinyl, furanyl and similar heterocyclic rings are specifically contemplated.
  • Selection of preferred restraining agents and their useful concentrations can be accomplished by the following selection procedure:
  • the compound being considered for use as a restraining agent is added to a silver chloride emulsion consisting essentially of cubic grains with a mean grain edge length of 0.3 ⁇ m.
  • the emulsion is 0.2 M in sodium acetate, has a pCl of 2.1, and has a pH that is at least one unit greater than the pKa of the compound being considered.
  • the emulsion is held at 75°C with the restraining agent present for 24 hours.
  • the compound introduced is performing the function of a restraining agent.
  • the significance of sharper edges of intersection of the ⁇ 100 ⁇ crystal faces lies in the fact that grain edges are the most active sites on the grains in terms of ions reentering the dispersing medium.
  • the restraining agent is acting to restrain the emergence of non- ⁇ 100 ⁇ crystal faces, such as are present, for example, at rounded edges and corners.
  • Optimum restraining agent activity occurs when the new grain population is a tabular grain population in which the tabular grains are bounded by ⁇ 100 ⁇ major crystal faces.
  • This example demonstrates the preparation of an ultrathin tabular grain silver iodochloride emulsion satisfying the requirements of this invention.
  • a 2030 mL solution containing 1.75% by weight low methionine gelatin, 0.011 M sodium chloride and 1.48 x 10 -4 M potassium iodide was provided in a stirred reaction vessel.
  • the contents of the reaction vessel were maintained at 40°C and the pCl was 1.95.
  • the mixture was then held 10 minutes with the temperature remaining at 40°C. Following the hold, a 1.0 M silver nitrate solution and a 1.0 M NaCl solution were then added simultaneously at 2 mL/min for 40 minutes with the pCl being maintained at 1.95.
  • the resulting emulsion was a tabular grain silver iodochloride emulsion containing 0.5 mole percent iodide, based on silver.
  • Fifty percent of total grain projected area was provided by tabular grains having ⁇ 100 ⁇ major faces having an average ECD of 0.84 mm and an average thickness of 0.037 ⁇ m, selected on the basis of an aspect ratio rank ordering of all ⁇ 100 ⁇ tabular grains having a thickness of less than 0.3 ⁇ m and a major face edge length ratio of less than 10.
  • the selected tabular grain population had an average aspect ratio (ECD/t) of 23 and an average tabularity (ECD/t 2 ) of 657.
  • the ratio of major face edge lengths of the selected tabular grains was 1.4.
  • tabular grains having ⁇ 100 ⁇ major faces and aspect ratios of at least 7.5. These tabular grains had a mean ECD of 0.75 ⁇ m, a mean thickness of 0.045 ⁇ m, a mean aspect ratio of 18.6 and a mean tabularity of 488.
  • This emulsion demonstrates the importance of iodide in the precipitation of the initial grain population (nucleation).
  • This emulsion was precipitated identically to that of Example 1, except no iodide was intentionally added.
  • the resulting emulsion consisted primarily of cubes and very low aspect ratio rectangular grains ranging in size from about 0.1 to 0.5 ⁇ m in edge length. A small number of large rods and high aspect ratio ⁇ 100 ⁇ tabular grains were present, but did not constitute a useful quantity of the grain population.
  • This example demonstrates an emulsion according to the invention in which 90% of the total grain projected area is comprised of tabular grains with ⁇ 100 ⁇ major faces and aspect ratios of greater than 7.5.
  • a 2030 mL solution containing 3.52% by weight low methionine gelatin, 0.0056 M sodium chloride and 1.48 x 10 -4 M potassium iodide was provided in a stirred reaction vessel.
  • the contents of the reaction vessel were maintained at 40°C and the pCl was 2.25.
  • the mixture was then held 10 minutes with the temperature remaining at 40°C. Following the hold, a 0.5 M silver nitrate solution and a 0.5 M NaCl solution were then added simultaneously at 8 mL/min for 40 minutes with the pCl being maintained at 2.25. The 0.5 M AgNO 3 solution and the 0.5 M NaCl solution were then added simultaneously with a ramped linearly increasing flow from 8 mL per minute to 16 mL per minute over 130 minutes with the pCl maintained at 2.25.
  • the resulting emulsion was a tabular grain silver iodochloride emulsion containing 0.06 mole percent iodide, based on silver.
  • Fifty percent of total grain projected area was provided by tabular grains having ⁇ 100 ⁇ major faces having an average ECD of 1.86 ⁇ m and an average thickness of 0.082 ⁇ m, selected on the basis of an aspect ratio rank ordering of all ⁇ 100 ⁇ tabular grains having a thickness of less than 0.3 ⁇ m and a major face edge length ratio of less than 10.
  • the selected tabular grain population had an average aspect ratio (ECD/t) of 24 and an average tabularity (ECD/t 2 ) of 314.
  • the ratio of major face edge lengths of the selected tabular grains was 1.2.
  • tabular grains having ⁇ 100 ⁇ major faces and aspect ratios of at least 7.5. These tabular grains had a mean ECD of 1.47 ⁇ m, a mean thickness of 0.086 ⁇ m, a mean aspect ratio of 17.5 and a mean tabularity of 222.
  • This example demonstrates an emulsion prepared similarly as the emulsion of Example 3, but an initial 0.08 mole percent iodide and a final 0.04% iodide.
  • a 2030 mL solution containing 3.52% by weight low methionine gelatin, 0.0056 M sodium chloride and 3.00 x 10 -5 M potassium iodide was provided in a stirred reaction vessel.
  • the contents of the reaction vessel were maintained at 40°C and the pCl was 2.25.
  • the mixture was then held 10 minutes with the temperature remaining at 40°C. Following the hold, a 0.5 M silver nitrate solution and a 0.5 M sodium chloride solution were then added simultaneously at 8 mL/min for 40 minutes with the pCl being maintained at 2.25.
  • the resulting emulsion was a tabular grain silver iodochloride emulsion containing 0.04 mole percent iodide, based on silver. Fifty percent of the total grain projected area was provided by tabular grains having ⁇ 100 ⁇ major faces having an average ECD of 0.67 ⁇ m and an average thickness of 0.035 ⁇ m, selected on the basis of an aspect ratio rank ordering of all ⁇ 100 ⁇ tabular grains having a thickness of less than 0.3 ⁇ m and a major face edge length ratio of less than 10.
  • the selected tabular grain population had an average aspect ratio (ECD/t) of 20 and an average tabularity (ECD/t 2 ) of 651. The ratio of major face edge lengths of the selected tabular grains was 1.9.
  • tabular grains having ⁇ 100 ⁇ major faces and aspect ratios of at least 7.5. These tabular grains had a mean ECD of 0.63 ⁇ m, a mean thickness of 0.036 ⁇ m, a mean aspect ratio of 18.5 and a mean tabularity of 595.
  • This example demonstrates an emulsion in which the initial grain population contained 6.0 mole percent iodide and the final emulsion contained 1.6% iodide.
  • a 2030 mL solution containing 3.52% by weight low methionine gelatin, 0.0056 M sodium chloride and 3.00 x 10 -5 M potassium iodide was provided in a stirred reaction vessel.
  • the contents of the reaction vessel were maintained at 40°C and the pCl was 2.25.
  • the mixture was then held 10 minutes with the temperature remaining at 40°C. Following the hold, a 1.00 M silver nitrate solution and a 1.00 M sodium chloride solution were then added simultaneously at 2 mL/min for 40 minutes with the pCl being maintained at 2.25.
  • the resulting emulsion was a tabular grain silver iodochloride emulsion containing 1.6 mole percent iodide, based on silver.
  • Fifty percent of total grain projected area was provided by tabular grains having ⁇ 100 ⁇ major faces having an average ECD of 0.57 ⁇ m and an average thickness of 0.036 ⁇ m, selected on the basis of an aspect ratio rank ordering of all ⁇ 100 ⁇ tabular grains having a thickness of less than 0.3 ⁇ m and a major face edge length ratio of less than 10.
  • the selected tabular grain population had an average aspect ratio (ECD/t) of 16.2 and an average tabularity (ECD/t 2 ) of 494.
  • the ratio of major face edge lengths of the selected tabular grains was 1.9.
  • tabular grains having ⁇ 100 ⁇ major faces and aspect ratios of at least 7.5. These tabular grains had a mean ECD of 0.55 ⁇ m, a mean thickness of 0.041 ⁇ m, a mean aspect ratio of 14.5 and a mean tabularity of 421.
  • This example demonstrates an ultrathin high aspect ratio ⁇ 100 ⁇ tabular grain emulsion in which 2 mole percent iodide is present in the initial population and additional iodide is added during growth to make the final iodide level 5 mole percent.
  • a 2030 mL solution containing 1.75% by weight low methionine gelatin, 0.0056 M sodium chloride and 1.48 x 10 -4 M potassium iodide was provided in a stirred reaction vessel.
  • the contents of the reaction vessel were maintained at 40°C and the pCl was 2.3.
  • the mixture was then held 10 minutes with the temperature remaining at 40°C. Following the hold, a 1.00 M silver nitrate solution and a 1.00 M sodium chloride solution were then added simultaneously at 8 mL/min while a 3.75 x 10 -3 M potassium iodide was simultaneously added at 14.6 mL/min for 10 minutes with the pCl being maintained at 1.95.
  • the resulting emulsion was a tabular grain silver iodochloride emulsion containing 5 mole percent iodide, based on silver. Fifty percent of total grain projected area was provided by tabular grains having ⁇ 100 ⁇ major faces having an average ECD of 0.58 ⁇ m and an average thickness of 0.030 ⁇ m, selected on the basis of an aspect ratio rank ordering of all ⁇ 100 ⁇ tabular grains having a thickness of less than 0.3 ⁇ m and a major face edge length ratio less than 10.
  • the selected tabular grain population had an average aspect ratio (ECD/t) of 20.6 and an average tabularity (ECD/t 2 ) of 803. The ratio of major face edge lengths of the selected tabular grains was 2.
  • This example demonstrates a high aspect ratio ⁇ 100 ⁇ tabular emulsion where 1 mole percent iodide is present in the initial grain population and 50 mole percent bromide is added during growth to make the final emulsion 0.3 mole percent iodide, 36 mole percent bromide and 63.7 mole percent chloride.
  • a 2030 mL solution containing 3.52% by weight low methionine gelatin, 0.0056 M sodium chloride and 1.48 x 10 -4 M potassium iodide was provided in a stirred reaction vessel.
  • the contents of the reaction vessel were maintained at 40°C and the pCl was 2.25.
  • the resulting emulsion was a tabular grain silver iodobromochloride emulsion containing 0.27 mole percent iodide and 36 mole percent bromide, based on silver, the remaining halide being chloride.
  • Fifty percent of total grain projected area was provided by tabular grains having ⁇ 100 ⁇ major faces having an average ECD of 0.4 ⁇ m and an average thickness of 0.032 ⁇ m, selected on the basis of an aspect ratio rank ordering of all ⁇ 100 ⁇ tabular grains having a thickness of less than 0.3 ⁇ m and a major face edge length ratio of less than 10.
  • the selected tabular grain population had an average aspect ratio (ECD/t) of 12.8 and an average tabularity (ECD/t 2 ) of 432.
  • the ratio of major face edge lengths of the selected tabular grains was 1.9. Seventy one percent of total grain projected area was made up of tabular grains having ⁇ 100 ⁇ major faces and aspect ratios of at least 7.5. These tabular grains had a mean ECD of 0.38 mm, a mean thickness of 0.034 ⁇ m, a mean aspect ratio of 11.3 and a mean tabularity of 363.
  • This example demonstrates the preparation of an emulsion satisfying the requirements of the invention employing phthalated gelatin as a peptizer.
  • the mixture was then held 10 minutes with the temperature remaining at 40°C. Following the hold, the silver and salt solutions were added simultaneously with a linearly accelerated flow from 3.0 mL/min to 9.0 mL/min over 15 minutes with the pCl of the mixture being maintained at 2.7.
  • the resulting emulsion was a high aspect ratio tabular grain silver iodochloride emulsion.
  • Fifty percent of total grain projected area was provided by tabular grains having ⁇ 100 ⁇ major faces having an average ECD of 0.37 ⁇ m and an average thickness of 0.037 ⁇ m, selected on the basis of an aspect ratio rank ordering of all ⁇ 100 ⁇ tabular grains having a thickness of less than 0.3 ⁇ m and a major face edge length ratio of less than 10.
  • the selected tabular grain population had an average aspect ratio (ECD/t) of 10 and an average tabularity (ECD/t 2 ) of 330.
  • Seventy percent of total grain projected area was made up of tabular grains having ⁇ 100 ⁇ major faces and aspect ratios of at least 7.5. These tabular grains had a mean ECD of 0.3 ⁇ m, a mean thickness of 0.04 ⁇ m, and a mean tabularity of 210.
  • Electron diffraction examination of the square and rectangular surfaces of the tabular grains confirmed major face ⁇ 100 ⁇ crystallographic orientation.
  • This example demonstrates the preparation of an emulsion satisfying the requirements of the invention employing an unmodified bone gelatin as a peptizer.
  • the mixture was then held for 5 minutes during which a 5000 mL solution that is 16.6 g/L of low methionine gelatin was added and the pH was adjusted to 6.5 and the pCl to 2.25. Following the hold, the silver and salt solutions were added simultaneously with a linearly accelerated flow from 10 mL/min to 25.8 mUmin over 63 minutes with the pCl of the mixture being maintained at 2.25.
  • the resulting emulsion was a high aspect ratio tabular grain silver iodochloride emulsion containing 0.01 mole % iodide. About 65% of the total projected grain area was provided by tabular grains having an average diameter of 1.5 ⁇ m and an average thickness of 0.18 ⁇ m.
  • This example compares the photographic performance of a ⁇ 100 ⁇ silver chloride tabular emulsion according to the invention to a silver chloride cubic grain emulsion of similar average grain volume.
  • Emulsion A Silver chloride tabular emulsion with ⁇ 100 ⁇ major faces
  • a 6090 ml solution containing 3.52% by weight of low methionine gelatin, 0.0056 M sodium chloride and 1.48 x 10 -4 potassium iodide was provided in a stirred reaction vessel at 40°C. While the solution was vigorously stirred, 90 mL of 2.0 M silver nitrate and 90 mL of a 1.99 M sodium chloride and 0.01 M potassium iodide solution were added simultaneously at a rate of 180 mL/min each. The mixture was then held for 10 minutes with the temperature remaining at 40°C.
  • a 0.5 M silver nitrate solution and a 0.5 M sodium chloride solution were added simultaneously at 24 mL/min for 40 minutes followed by a linear acceleration from 24 mL/min to 48 mL/min over 130 minutes, while maintaining the pCl at 2.25.
  • the pCl was then adjusted to 1.30 with sodium chloride then washed using ultrafiltration to a pCl of 2.0 then adjusted to a pCl of 1.65 with sodium chloride.
  • the resulting emulsion was a tabular grain silver chloride emulsion contained 0.06 mole percent iodide and had a mean equivalent circular grain diameter of 1.45 ⁇ m and a mean grain thickness of 0.13 ⁇ m.
  • Emulsion A An optimum green light sensitization was found for Emulsion A by conducting numerous small scale finishing experiments where the level of sensitizing dye, sodium thiosulfate pentahydrate, aurous dithiosulfate dihydrate and the hold time at 65°C were varied.
  • the optimum finish was as follows: to a 0.5 mole portion of Emulsion A melted at 40°C and well stirred, 0.800 mmol/mole of green light sensitizing dye A was added followed by a 20 minute hold. To this was added 0.10 mg/mole of sodium thiosulfate pentahydrate and 0.20 mg/mole of sodium aurous dithiosulfate dihydrate. The temperature was then increased to 65°C over 9 minutes and then held for 4 minutes at 65°C and rapidly cooled to 40°C.
  • Emulsion B Silver chloride cubic grain emulsion (Control)
  • a monodisperse silver chloride cube with a cubic edge length of 0.59 ⁇ m was prepared by simultaneous addition of 3.75 M silver nitrate and 3.75 M sodium chloride to a well stirred solution containing 8.2 g/l of sodium chloride, 28.2 g/l of bone gelatin and 0.212 g/liter of 1,8-dithiadioctanediol while maintaining the temperature at 68.3°C and the pCl at 1.0.
  • the temperature was reduced to 40°C and the emulsion was washed by ultrafiltration to a pCl of 2.0, then adjusted to a pCl of 1.65 with sodium chloride.
  • Emulsion A An optimum green light sensitization was found in the same manner as described for Emulsion A.
  • the conditions for the optimum were as follows: to a 0.05 mole quantity of Emulsion B melted at 40°C and well stirred, 0.2 mmol/mole of sensitizing dye A was added followed by a 20 minute hold. To this was added 0.25 mg/mole of sodium thiosulfate pentahydrate and 0.50 mg/mole of sodium aurous dithiosulfate dihydrate. The temperature was then increased to 65°C over 9 minutes and held for 10 minutes followed by rapid cooling to 40°C.
  • Each of the sensitized emulsions was coated on antihalation support at 0.85 g/m 2 of silver along with 1.1 g/m 2 of cyan dye-forming coupler C and 2.7 g/m 2 of gelatin. This was overcoated with 1.6 g/m 2 of gelatin and hardened with 1.7 weight percent, based on total gelatin, of bis(vinyl-sulfonylmethyl)ether.
  • the coatings were evaluated for intrinsic sensitivity by exposing for 0.02 seconds in a step wedge sensitometer with the 365 nm line of a mercury vapor lamp as the light source.
  • Sensitivity to green light was measured by exposing the coatings for 0.02 seconds using a step wedge sensitometer with a 3000°K tungsten lamp filtered to simulate a Daylight V light source and filtered to transmit only green and red light by a Kodak WrattenTM 9 filter (transmitting wavelengths longer than 450 nm).
  • the coatings were processed using a standard C-41TM color negative process and the dye density was measured using status M red filtration.
  • Table I The photographic results are summarized in Table I.
  • Table I 365 line exposure Wratten 9TM exposure Emulsion Dmin speed contrast Dmin speed contrast Emulsion A (tab.) unsensitized 0.06 10 1.75 --- --- green sensitized 0.22 129 1.96 .22 371 2.08 Emulsion B (cubic) unsensitized 0.06 7 4.03 --- --- green sensitized 0.22 120 2.89 .16 128 2.86
  • Table I shows that for intrinsic sensitivity as measured by the 365 line exposure, both Emulsions A and B are very similar as would be expected based on their similar grain volume. Comparing the green light sensitivity as measured by the Wratten 9 exposures shows that the tabular emulsion is 2.9 times more sensitive to green light than the cubic emulsion. This clearly shows the advantage of the tabular morphology.
  • a stirred reaction vessel containing 400 mL of a solution which was 0.5% in bone gelatin, 6mM in 3-amino-1H-1,2,4-triazole, 0.040 M in NaCl, and 0.20 M in sodium acetate was adjusted to pH 6.1 at 55°C.
  • To this solution at 55°C were added simultaneously 5.0 mL of 4 M AgNO 3 and 5.0 mL of 4 M NaCl at a rate of 5 mL/min each. The temperature of the mixture was then increased to 75°C at a constant rate requiring 12 min and then held at this temperature for 5 min.
  • the pH was adjusted to 6.2 and held to within ⁇ 0.1 of this value, and the flow of the AgNO 3 solution was resumed at 5 mL/min until 0.8 mole of Ag had been added.
  • the flow of the NaCl solution was also resumed at a rate needed to maintain a constant pAg of 6.64.
  • the resulting AgCl emulsion consisted of tabular grains having ⁇ 100 ⁇ major faces which made up 65% of the projected area of the total grain population.
  • This tabular grain population had a mean equivalent circular diameter of 1.95 ⁇ m and a mean thickness of 0.165 ⁇ m.
  • the average aspect ratio and tabularity were 11.8 and 71.7, respectively.
  • This emulsion is shown in Fig. 3.
  • This emulsion was prepared similar to that of Example 11A except that the precipitation was stopped when 0.4 mole of Ag had been added.
  • the resulting emulsion consisted of tabular grain having ⁇ 100 ⁇ major faces which made up 65% of the projected area of the total grain population.
  • This tabular grain population had a mean equivalent circular diameter of 1.28 ⁇ m and a mean thickness of 0.130 ⁇ m.
  • the average aspect ratio and tabularity were 9.8 and 75.7, respectively.
  • This emulsion is shown in Figs. 4 and 5.
  • This example was prepared similar to that of Example 11B except that the pH of the reaction vessel was adjusted to 3.6 for the last 95% of the AgNO 3 addition.
  • the resulting emulsion consisted of ⁇ 100 ⁇ tabular grains making up 60% of the projected area of the total grain population.
  • This tabular grain population had a mean equivalent circular diameter of 1.39 ⁇ m, and a mean thickness of 0.180 ⁇ m.
  • the average aspect ratio and tabularity were 7.7 and 43.0, respectively.
  • This emulsion was prepared similar to that of Example 11B except that the salt solution was 3.6 M in NaCl and 0.4 M in NaBr.
  • the resulting AgBrCl (10% Br) emulsion consisted of ⁇ 100 ⁇ tabular grain making up 52% of the projected area of the total grain population.
  • This tabular grain population had a mean equivalent circular diameter of 1.28 ⁇ m, and a mean thickness of 0.115.
  • the average aspect ratio and tabularity were 11.1 and 96.7, respectively.
  • Example 11 A An emulsion was prepared similar to that of Example 11 A except that the precipitation was scaled-up five times so that 4.0 moles of AgCl were precipitated.
  • the resulting ⁇ 100 ⁇ tabular grain emulsion was cooled to 40°C, poured into 4 L of distilled water and allowed to gravity settle for 24 hours at 2°C. The settled phase was discarded.
  • To the supernatant was added 12 g of phthalated gelatin and the emulsion was washed by the coagulation method of U.S. Patent 2,614,929.
  • the resulting 2.2 moles of emulsion consisted of tabular grains having ⁇ 100 ⁇ major faces which made up 80% of the projected area of the total grain population.
  • This tabular grain population had a mean equivalent circular diameter of 1.81 ⁇ m and a mean thickness of 0.173 ⁇ m (measuring >10 6 grains).
  • the average aspect ratio and tabularity were 10.5 and 60.5, respectively.
  • the emulsion was diluted to 1 Kg emulsion/mole AgCl and adjusted to a pAg of 7.42 with NaCl solution and pH of 5.3 at 40°C. It was divided into portions for spectral and chemical sensitizations.
  • portions C and D were then added 10 mg Au 2 S/mole AgCl.
  • 2.0 mole% NaBr as a 1 M solution, was added to portions A, B, C and D.
  • Portions C and D were heated for 20 minutes at 60°C. Scanning electron images show that all portions retained their ⁇ 100 ⁇ tabular grain content, and portion B had AgClBr epitaxial growths at the grains edges and corners.
  • These portions were coated on polyester film support at 2.6 g silver/m 2 and 3.4 g gelatin/m 2 to make coatings A, B, C, and D, respectively.
  • the coatings were exposed for 0.5 sec to a 600W 3,000 K tungsten light source through a 0-4.0 density step tablet and a Kodak WrattenTM filter.
  • Coatings A and C were exposed through a Kodak WrattenTM 99 green filter while Coatings B an D were exposed through a Kodak WrattenTM 2B yellow filter. Another set of coatings were exposed on a variable wavelength, variable intensity wedge spectrograph.

Landscapes

  • Chemical & Material Sciences (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)
  • Peptides Or Proteins (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Claims (16)

  1. Strahlungsempfindliche Emulsion, enthaltend eine Silberhalogenid-Kornpopulation, die mindestens 50 Mol-% Chlorid, bezogen auf das gesamte Silber, das die projizierte Fläche der Kornmpopulation ausmacht, enthält, in der mehr als 50 % der projizierten Fläche der Kornpopulation zurückzuführen sind auf tafelförmige Körner mit einer mittleren Dicke von weniger als 0,3 µm, und worin die tafelförmigen Körner parallele Hauptflächen aufweisen, die in {100} kristallographischen Ebenen liegen.
  2. Strahlungsempfindliche Emulsion nach Anspruch 1, in der mehr als 70 % der gesamten projizierten Kornfläche auf tafelförmigen Körnern beruhen, die {100} Hauptflächen aufweisen und die eine Dicke von weniger als 0,3 µm haben.
  3. Strahlungsempfindliche Emulsion nach Anspruch 1, in der mehr als 50 % der gesamten projizierten Kornfläche auf tafelförmige Körner entfallen, die {100} Hauptflächen aufweisen und eine Dicke von weniger als 0,2 µm haben.
  4. Strahlungsempfindliche Emulsion nach Anspruch 1 oder 2, weiter dadurch gekennzeichnet, daß von den tafelförmigen Körnern, die durch {100} Hauptflächen begrenzt sind, ein Teil, der 50 % der gesamten projizierten Kornfläche ausmacht, ausgewählt nach den Kriterien der Kantenverhältnisse der benachbarten Hauptflächen von weniger als 10 und Dicken von weniger als 0,3 µm und mit höheren Aspektverhältnissen als irgendwelche übrigen tafelförmigen Körner, die diesen Kriterien genügen, haben (1) ein mittleres Aspektverhältnis von mehr als 8 und (2) intern an ihren Keimbildungszentren Iodid enthalten und mindestens 50 Mol-% Chlorid.
  5. Strahlungsempfindliche Emulsion nach Anspruch 4, weiter dadurch gekennzeichnet, daß der ausgewählte Teil der tafelförmigen Körner ein mittleres Aspektverhältnis von größer als 12 aufweist.
  6. Strahlungsempfindliche Emulsion nach Anspruch 4 oder 5, weiter dadurch gekennzeichnet, daß der ausgewählte Teil der tafelförmigen Körner Kantenverhältnisse von benachbarten Hauptflächen von weniger als 5 aufweist.
  7. Strahlungsempfindliche Emulsion nach Anspruch 6, weiter dadurch gekennzeichnet, daß der ausgewählte Teil der tafelförmigen Körner Kantenverhältnisse der benachbarten Hauptflächen von weniger als 2 hat.
  8. Strahlungsempfindliche Emulsion nach einem der Ansprüche 4 bis 7 einschließlich, weiter dadurch gekennzeichnet, daß der ausgewählte Teil der tafelförmigen Körner ultradünne tafelförmige Körner mit Dicken von weniger als 0,06 µm sind.
  9. Strahlungsempfindliche Emulsion nach einem der Ansprüche 1 bis 8 einschließlich, weiter dadurch gekennzeichnet, daß die tafelförmigen Körner mindestens 90 Mol-% Chlorid enthalten.
  10. Verfahren zur Herstellung von Silberhalogenidemulsionen nach Anspruch 4, bestehend aus den Schritten
    (1) Einführung von Silber- und Halogenidsalzen in ein Dispersionsmedium derart, daß eine Keimbildung der tafelförmigen Körner in Gegenwart von Iodid erfolgt, wobei Chlorid mindestens 50 Mol-% des Halogenides ausmacht, das in dem Dispersionsmedium vorhanden ist und wobei der pCl-Wert des Dispersionsmediums im Bereich von 0,5 bis 3,5 gehalten wird, und
    (2) nachfolgende, das Kornwachstum vervollständigende Keimbildung, durch Zusatz von Silber- und Halogenidsalzen in das Dispersionsmedium unter Bedingungen, die die {100} Hauptflächen der tafelförmigen Körner aufrechterhalten.
  11. Verfahren nach Anspruch 10, weiter dadurch gekennzeichnet, daß Bromidionen in dem Dispersionsmedium nach der Kornkeimbildung vorhanden sind.
  12. Verfahren nach Anspruch 10 oder 11, weiter dadurch gekennzeichnet, daß die Kornkeimbildung in Gegenwart von Halogenidionen durchgeführt wird, die im wesentlichen aus Chlorid- und Iodidionen bestehen, wobei der pCl-Wert des Dispersionsmediums im Bereich von 1,0 bis 3,0 gehalten wird und ein Gelatino-Peptisationsmittel vorliegt mit einem Methioningehalt von weniger als 30 Mikromolen pro Gramm Peptisationsmittel.
  13. Verfahren nach Anspruch 12, weiter dadurch gekennzeichnet, daß die Kornkeimbildung in Gegenwart von Halogenidionen erfolgt, die im wesentlichen aus Chlorid- und Iodidionen bestehen, wobei der pCl-Wert des Dispersionsmediums im Bereich von 1,5 bis 2,5 liegt und ein Gelatino-Peptisationsmittel mit einem Methioningehalt von weniger als 12 Mikromolen pro Gramm Peptisationsmittel vorliegt.
  14. Verfahren nach den Ansprüchen 10 bis 13, weiter dadurch gekennzeichnet, dass die Zugabe der Silber- und Halogenidsalzlösungen nach der Kornkeimbildung suspendiert wird, um eine Ostwald-Reifung der Kornkeime zu ermöglichen, und dann wieder aufgenommen wird.
  15. Verfahren nach Anspruch 14, weiter dadurch gekennzeichnet, dass die Chlorid- und Iodidsalzlösungen in das Dispersionsmedium während der Kornkeimbildung eingeführt werden.
  16. Verfahren nach Anspruch 14 oder 15, weiter dadurch gekennzeichnet, dass Bromidsalzlösungen in das Dispersionsmedium eingeführt wird, nachdem die Salzlösungseinführung wieder aufgenommen wurde, nachdem die Zugabe der Silber- und Halogenidsalzlösungen suspendiert wurde, um eine Ostwald-Reifung der Kornkeime zu ermöglichen.
EP92116262A 1991-09-24 1992-09-23 Hochchloridhaltige Emulsionen hoher Tafelförmigkeit von aussergewöhnlicher Stabilität Expired - Lifetime EP0534395B2 (de)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US76486891A 1991-09-24 1991-09-24
US764868 1991-09-24
US82633892A 1992-01-27 1992-01-27
US826338 1992-01-27

Publications (3)

Publication Number Publication Date
EP0534395A1 EP0534395A1 (de) 1993-03-31
EP0534395B1 EP0534395B1 (de) 1998-11-11
EP0534395B2 true EP0534395B2 (de) 2006-04-12

Family

ID=27117531

Family Applications (1)

Application Number Title Priority Date Filing Date
EP92116262A Expired - Lifetime EP0534395B2 (de) 1991-09-24 1992-09-23 Hochchloridhaltige Emulsionen hoher Tafelförmigkeit von aussergewöhnlicher Stabilität

Country Status (8)

Country Link
EP (1) EP0534395B2 (de)
JP (1) JP3243010B2 (de)
AT (1) ATE173341T1 (de)
AU (1) AU2599492A (de)
DE (1) DE69227567T3 (de)
DK (1) DK0534395T3 (de)
ES (1) ES2123532T3 (de)
WO (1) WO1993006521A1 (de)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5298385A (en) * 1992-06-15 1994-03-29 Eastman Kodak Company High chloride folded tabular grain emulsions
US5275930A (en) * 1992-08-27 1994-01-04 Eastman Kodak Company High tabularity high chloride emulsions of exceptional stability
EP0616255B1 (de) * 1993-03-18 1999-09-15 Kodak Limited Farbphotographisches Element mit niedrigem Silbergehalt und Verfahren zur Farbbildherstellung
US5310635A (en) * 1993-03-22 1994-05-10 Eastman Kodak Company Photographic camera film containing a high chloride tabular grain emulsion with tabular grain {100} major faces
JP3270614B2 (ja) * 1993-03-22 2002-04-02 イーストマン コダック カンパニー 中位アスペクト比平板状粒子乳剤
US5451490A (en) * 1993-03-22 1995-09-19 Eastman Kodak Company Digital imaging with tabular grain emulsions
US5443943A (en) * 1993-03-22 1995-08-22 Eastman Kodak Company Method of processing originating photographic elements containing tabular silver chloride grains bounded by {100} faces
WO1994022054A1 (en) * 1993-03-22 1994-09-29 Eastman Kodak Company Dye image forming photographic elements
DE69421838T2 (de) * 1993-03-22 2000-06-15 Eastman Kodak Co Verarbeitungsverfahren für photographische Originalelemente, die tafelförmige Silberchloridkörner begrenzt mit (100) Kornoberfläche enthalten
EP0617320A3 (de) * 1993-03-22 1995-02-01 Eastman Kodak Co Emulsionen mit tafelförmigen Körnern, die Antischleiermittel und Stabilisatoren enthalten.
US5264337A (en) * 1993-03-22 1993-11-23 Eastman Kodak Company Moderate aspect ratio tabular grain high chloride emulsions with inherently stable grain faces
JP2982097B2 (ja) * 1993-04-02 1999-11-22 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
JP3151094B2 (ja) * 1993-04-02 2001-04-03 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の画像形成方法
JP3058545B2 (ja) * 1993-04-02 2000-07-04 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
US5314798A (en) * 1993-04-16 1994-05-24 Eastman Kodak Company Iodide banded tabular grain emulsion
JPH07146522A (ja) * 1993-09-29 1995-06-06 Fuji Photo Film Co Ltd ハロゲン化銀乳剤
US5498511A (en) * 1993-10-25 1996-03-12 Fuji Photo Film Co., Ltd. Silver halide photographic material
DE69316899T2 (de) * 1993-11-16 1998-09-10 Agfa Gevaert Nv Chloridreiche Tafelkornemulsion mit (100)-Hauptflächen
US5593820A (en) * 1993-12-20 1997-01-14 Fuji Photo Film Co., Ltd. Silver halide emulsion and silver halide photographic material using the same
JPH07219100A (ja) * 1994-02-04 1995-08-18 Fuji Photo Film Co Ltd ハロゲン化銀乳剤およびこれを用いたハロゲン化銀写真感光材料
EP0670514A3 (de) * 1994-02-25 1996-01-17 Eastman Kodak Co Emulsionen, die chloridreiche, tafelförmige (100) Körner mit modifizierten Kantenstrukturen enthalten.
US5399477A (en) * 1994-02-25 1995-03-21 Eastman Kodak Company Silver halide photographic elements
US5395746A (en) * 1994-02-25 1995-03-07 Eastman Kodak Company Inherently stable high chloride tabular grains with improved blue absorption
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
US5413904A (en) * 1994-03-18 1995-05-09 Eastman Kodak Company High chloride [100] tabular grain emulsions improved emulsions and improved precipitation processes
US5434038A (en) * 1994-03-31 1995-07-18 Eastman Kodak Company Photographic image display material
EP0678772A1 (de) * 1994-04-06 1995-10-25 Agfa-Gevaert N.V. Lichtempfindliches Silberchlorobromojodid- oder Silbuchlorojodid-Tafelkörner enthaltendes Material
US5457021A (en) * 1994-05-16 1995-10-10 Eastman Kodak Company Internally doped high chloride {100} tabular grain emulsions
US5660974A (en) 1994-06-09 1997-08-26 Eastman Kodak Company Color developer containing hydroxylamine antioxidants
JPH08101477A (ja) 1994-08-01 1996-04-16 Eastman Kodak Co 水性写真用コーティング組成物
US5665530A (en) * 1994-08-30 1997-09-09 Fuji Photo Film Co., Ltd. Silver halide emulsion and photographic material using the same
US5807665A (en) * 1995-04-14 1998-09-15 Fuji Photo Film Co., Ltd. Silver halide emulsion
US5707793A (en) * 1995-04-19 1998-01-13 Fuji Photo Film Co., Ltd. Silver halide emulsion and silver halide photographic material using the same
JP3543047B2 (ja) * 1996-09-09 2004-07-14 富士写真フイルム株式会社 ハロゲン化銀乳剤およびハロゲン化銀カラー写真感光材料
JPH11271900A (ja) * 1998-01-20 1999-10-08 Fuji Photo Film Co Ltd ハロゲン化銀乳剤

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1507989A (en) * 1974-12-19 1978-04-19 Ciba Geigy Ag Photographic emulsions
US4386156A (en) * 1981-11-12 1983-05-31 Eastman Kodak Company Silver bromide emulsions of narrow grain size distribution and processes for their preparation
JPH0789203B2 (ja) * 1987-04-30 1995-09-27 富士写真フイルム株式会社 ハロゲン化銀乳剤および写真感光材料
JPH0242A (ja) * 1987-10-19 1990-01-05 Fuji Photo Film Co Ltd ハロゲン化銀写真感光材料

Also Published As

Publication number Publication date
ATE173341T1 (de) 1998-11-15
DK0534395T3 (da) 1999-07-26
EP0534395B1 (de) 1998-11-11
ES2123532T3 (es) 1999-01-16
JP3243010B2 (ja) 2002-01-07
WO1993006521A1 (en) 1993-04-01
EP0534395A1 (de) 1993-03-31
AU2599492A (en) 1993-04-27
DE69227567D1 (de) 1998-12-17
DE69227567T2 (de) 1999-05-06
JPH05204073A (ja) 1993-08-13
DE69227567T3 (de) 2006-10-26

Similar Documents

Publication Publication Date Title
EP0534395B2 (de) Hochchloridhaltige Emulsionen hoher Tafelförmigkeit von aussergewöhnlicher Stabilität
EP0672940B1 (de) Emulsionen enthaltend (1,0,0) tafelförmige hochchloridhaltige Körner: verbesserte Emulsionen und verbesserte Fällungsprozesse
EP0584815B1 (de) Emulsionen mit hoher Tafelförmigkeit und hohem Chloridgehalt von ungewöhnlicher Stabilität
EP0620479B1 (de) Emulsion mit Iodid-Streifen aufweisenden tafelförmigen Körnern
EP0534325B1 (de) Emulsionen mit ultradünnen tafelförmigen Körnern eines hohen Chloridgehaltes
EP0513724B1 (de) Verfahren zur Herstellung einer Emulsion mit tafelförmigen Körnern von verminderter Dispersität
US5389509A (en) Ultrathin high chloride tabular grain emulsions
EP0617318B1 (de) Digitale Bildherstellung mit Emulsionen tafelförmiger Körner
JP3025585B2 (ja) ハロゲン化銀乳剤
EP0430196B1 (de) Verfahren zur Stabilisierung von chloridreichen Kristallen mit modifiziertem Kristallhabitus durch Anwendung von Bromidhüllen
CA2076991A1 (en) Process for the preparation of high chloride tabular grain emulsions (iii)
EP0617319B1 (de) Film und Kamera
EP0616255B1 (de) Farbphotographisches Element mit niedrigem Silbergehalt und Verfahren zur Farbbildherstellung
JP3270614B2 (ja) 中位アスペクト比平板状粒子乳剤
EP0617322A1 (de) Verarbeitungsverfahren für photographische Originalelemente, die tafelförmige Silberchloridkörner begrenzt mit (100) Kornoberfläche enthalten
EP0645022B1 (de) Verfahren zur herstellung von tafelkornemulsionen
EP0617317A1 (de) Mit Oligomeren modifizierte Emulsionen tafelförmiger Körner
EP0577173B1 (de) Emulsionen mit chloridreichen gefalteten Tafelkörnern und Verfahren zu ihrer Herstellung
EP0871063B1 (de) Verfahren zur Herstellung einer Silberhalogenidemulsion
EP0678774A2 (de) Ablagerungssensibilisierte Emulsionen
EP0670514A2 (de) Emulsionen, die chloridreiche, tafelförmige (100) Körner mit modifizierten Kantenstrukturen enthalten

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

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LI LU MC NL PT SE

17P Request for examination filed

Effective date: 19930908

17Q First examination report despatched

Effective date: 19931028

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LI LU MC NL PT SE

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

Ref country code: CH

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19981111

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19981111

Ref country code: LI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19981111

REF Corresponds to:

Ref document number: 173341

Country of ref document: AT

Date of ref document: 19981115

Kind code of ref document: T

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REF Corresponds to:

Ref document number: 69227567

Country of ref document: DE

Date of ref document: 19981217

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2123532

Country of ref document: ES

Kind code of ref document: T3

ITF It: translation for a ep patent filed

Owner name: MODIANO & ASSOCIATI S.R.L.

REG Reference to a national code

Ref country code: CH

Ref legal event code: NV

Representative=s name: KIRKER & CIE SA

ET Fr: translation filed
REG Reference to a national code

Ref country code: PT

Ref legal event code: SC4A

Free format text: AVAILABILITY OF NATIONAL TRANSLATION

Effective date: 19981112

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

PLBQ Unpublished change to opponent data

Free format text: ORIGINAL CODE: EPIDOS OPPO

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

26 Opposition filed

Opponent name: FUJI PHOTO FILM CO., LTD.

Effective date: 19990811

NLR1 Nl: opposition has been filed with the epo

Opponent name: FUJI PHOTO FILM CO., LTD.

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

RDAH Patent revoked

Free format text: ORIGINAL CODE: EPIDOS REVO

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

Ref country code: MC

Payment date: 20010914

Year of fee payment: 10

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

Ref country code: MC

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

Effective date: 20010923

APAC Appeal dossier modified

Free format text: ORIGINAL CODE: EPIDOS NOAPO

APAE Appeal reference modified

Free format text: ORIGINAL CODE: EPIDOS REFNO

APAC Appeal dossier modified

Free format text: ORIGINAL CODE: EPIDOS NOAPO

REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

APBU Appeal procedure closed

Free format text: ORIGINAL CODE: EPIDOSNNOA9O

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

Ref country code: PT

Payment date: 20050622

Year of fee payment: 14

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

Ref country code: IE

Payment date: 20050630

Year of fee payment: 14

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

Ref country code: AT

Payment date: 20050701

Year of fee payment: 14

Ref country code: LU

Payment date: 20050701

Year of fee payment: 14

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

Ref country code: GR

Payment date: 20050726

Year of fee payment: 14

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

Ref country code: DK

Payment date: 20050808

Year of fee payment: 14

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

Ref country code: SE

Payment date: 20050905

Year of fee payment: 14

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

Ref country code: ES

Payment date: 20050916

Year of fee payment: 14

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

Ref country code: CH

Payment date: 20050927

Year of fee payment: 14

APAH Appeal reference modified

Free format text: ORIGINAL CODE: EPIDOSCREFNO

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

Ref country code: BE

Payment date: 20051006

Year of fee payment: 14

PUAH Patent maintained in amended form

Free format text: ORIGINAL CODE: 0009272

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

Free format text: STATUS: PATENT MAINTAINED AS AMENDED

27A Patent maintained in amended form

Effective date: 20060412

AK Designated contracting states

Kind code of ref document: B2

Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LI LU MC NL PT SE

REG Reference to a national code

Ref country code: CH

Ref legal event code: AEN

Free format text: MAINTIEN DU BREVET DONT L'ETENDUE A ETE MODIFIEE

NLR2 Nl: decision of opposition

Effective date: 20060412

NLR3 Nl: receipt of modified translations in the netherlands language after an opposition procedure
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20060712

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

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20060723

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

Ref country code: IE

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

Effective date: 20060925

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

Ref country code: IT

Payment date: 20060930

Year of fee payment: 15

ET3 Fr: translation filed ** decision concerning opposition
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

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

Effective date: 20070323

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: PT

Ref legal event code: MM4A

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

Effective date: 20070323

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

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

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20060713

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

Ref country code: LU

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

Effective date: 20060923

Ref country code: SE

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

Effective date: 20060924

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

Ref country code: BE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19981111

Ref country code: IT

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

Effective date: 20070923

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

Ref country code: DE

Payment date: 20100930

Year of fee payment: 19

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

Ref country code: FR

Payment date: 20110901

Year of fee payment: 20

Ref country code: GB

Payment date: 20110826

Year of fee payment: 20

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

Ref country code: NL

Payment date: 20110912

Year of fee payment: 20

REG Reference to a national code

Ref country code: DE

Ref legal event code: R071

Ref document number: 69227567

Country of ref document: DE

REG Reference to a national code

Ref country code: DE

Ref legal event code: R071

Ref document number: 69227567

Country of ref document: DE

REG Reference to a national code

Ref country code: NL

Ref legal event code: V4

Effective date: 20120923

REG Reference to a national code

Ref country code: GB

Ref legal event code: PE20

Expiry date: 20120922

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 EXPIRATION OF PROTECTION

Effective date: 20120922

Ref country code: DE

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20120925