US2628167A - Method of making colloid silver halide emulsions containing thallium - Google Patents
Method of making colloid silver halide emulsions containing thallium Download PDFInfo
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- US2628167A US2628167A US24102A US2410248A US2628167A US 2628167 A US2628167 A US 2628167A US 24102 A US24102 A US 24102A US 2410248 A US2410248 A US 2410248A US 2628167 A US2628167 A US 2628167A
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- silver
- emulsion
- thallous
- soluble
- water
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- 239000000839 emulsion Substances 0.000 title claims description 67
- 229910052709 silver Inorganic materials 0.000 title claims description 37
- 239000004332 silver Substances 0.000 title claims description 37
- -1 silver halide Chemical class 0.000 title claims description 28
- 239000000084 colloidal system Substances 0.000 title claims description 18
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 229910052716 thallium Inorganic materials 0.000 title description 9
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 title description 7
- 150000003839 salts Chemical class 0.000 claims description 22
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 12
- 150000004820 halides Chemical class 0.000 claims description 12
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 claims description 10
- 230000001376 precipitating effect Effects 0.000 claims description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 22
- 235000002639 sodium chloride Nutrition 0.000 description 22
- 239000008273 gelatin Substances 0.000 description 16
- 229920000159 gelatin Polymers 0.000 description 16
- 108010010803 Gelatin Proteins 0.000 description 15
- 235000019322 gelatine Nutrition 0.000 description 15
- 235000011852 gelatine desserts Nutrition 0.000 description 15
- 239000000243 solution Substances 0.000 description 14
- FYWSTUCDSVYLPV-UHFFFAOYSA-N nitrooxythallium Chemical compound [Tl+].[O-][N+]([O-])=O FYWSTUCDSVYLPV-UHFFFAOYSA-N 0.000 description 13
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Substances [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 11
- 230000005070 ripening Effects 0.000 description 11
- 229910001961 silver nitrate Inorganic materials 0.000 description 11
- 238000000586 desensitisation Methods 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 239000013078 crystal Substances 0.000 description 8
- 238000001556 precipitation Methods 0.000 description 6
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 5
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 4
- 229910001502 inorganic halide Inorganic materials 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 230000029087 digestion Effects 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 230000001235 sensitizing effect Effects 0.000 description 3
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- 238000001016 Ostwald ripening Methods 0.000 description 2
- 206010034960 Photophobia Diseases 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000004694 iodide salts Chemical class 0.000 description 2
- 208000013469 light sensitivity Diseases 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 150000003475 thallium Chemical class 0.000 description 2
- AGJZCWVTGOVGBS-UHFFFAOYSA-N 1,1'-diethyl-2,2'-cyanine Chemical compound C1=CC2=CC=CC=C2N(CC)\C1=C\C1=CC=C(C=CC=C2)C2=[N+]1CC AGJZCWVTGOVGBS-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 241000206672 Gelidium Species 0.000 description 1
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical class OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical class [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229920002494 Zein Polymers 0.000 description 1
- FQNGWRSKYZLJDK-UHFFFAOYSA-N [Ca].[Ba] Chemical compound [Ca].[Ba] FQNGWRSKYZLJDK-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 235000010419 agar Nutrition 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- OIDPCXKPHYRNKH-UHFFFAOYSA-J chrome alum Chemical compound [K]OS(=O)(=O)O[Cr]1OS(=O)(=O)O1 OIDPCXKPHYRNKH-UHFFFAOYSA-J 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- FDWREHZXQUYJFJ-UHFFFAOYSA-M gold monochloride Chemical compound [Cl-].[Au+] FDWREHZXQUYJFJ-UHFFFAOYSA-M 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- CBEQRNSPHCCXSH-UHFFFAOYSA-N iodine monobromide Chemical compound IBr CBEQRNSPHCCXSH-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229960002523 mercuric chloride Drugs 0.000 description 1
- LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 235000007715 potassium iodide Nutrition 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- CQLFBEKRDQMJLZ-UHFFFAOYSA-M silver acetate Chemical compound [Ag+].CC([O-])=O CQLFBEKRDQMJLZ-UHFFFAOYSA-M 0.000 description 1
- 229940071536 silver acetate Drugs 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical class [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- 229940071575 silver citrate Drugs 0.000 description 1
- YPNVIBVEFVRZPJ-UHFFFAOYSA-L silver sulfate Chemical compound [Ag+].[Ag+].[O-]S([O-])(=O)=O YPNVIBVEFVRZPJ-UHFFFAOYSA-L 0.000 description 1
- 229910000367 silver sulfate Inorganic materials 0.000 description 1
- TZMGLOFLKLBEFW-UHFFFAOYSA-M silver;sulfamate Chemical compound [Ag+].NS([O-])(=O)=O TZMGLOFLKLBEFW-UHFFFAOYSA-M 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- YTQVHRVITVLIRD-UHFFFAOYSA-L thallium sulfate Chemical compound [Tl+].[Tl+].[O-]S([O-])(=O)=O YTQVHRVITVLIRD-UHFFFAOYSA-L 0.000 description 1
- VNJJMQRBCYQGFL-UHFFFAOYSA-N thallium(1+);cyanide Chemical compound [Tl+].N#[C-] VNJJMQRBCYQGFL-UHFFFAOYSA-N 0.000 description 1
- HQOJMTATBXYHNR-UHFFFAOYSA-M thallium(I) acetate Chemical compound [Tl+].CC([O-])=O HQOJMTATBXYHNR-UHFFFAOYSA-M 0.000 description 1
- 229910000374 thallium(I) sulfate Inorganic materials 0.000 description 1
- CULOEOTWMUCRSJ-UHFFFAOYSA-M thallium(i) fluoride Chemical compound [Tl]F CULOEOTWMUCRSJ-UHFFFAOYSA-M 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- QUTYHQJYVDNJJA-UHFFFAOYSA-K trisilver;2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Ag+].[Ag+].[Ag+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QUTYHQJYVDNJJA-UHFFFAOYSA-K 0.000 description 1
- PBYZMCDFOULPGH-UHFFFAOYSA-N tungstate Chemical compound [O-][W]([O-])(=O)=O PBYZMCDFOULPGH-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000005019 zein Substances 0.000 description 1
- 229940093612 zein Drugs 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
Definitions
- This invention relates to photographic elements, to light-sensitive silver halide emulsions and to their preparation. More particularly it relates to photographic elements bearing a colloid silver halide emulsion layer which contains a small amount of thallium.
- An object of this invention is to provide photographic silver halide emulsion layers which are more resistant to local desensitization due to abrasive forces.
- a related object is to provide flexible photographic elements with silver halide emulsion layers which are more resistant to desensitization due to kinking.
- a further object is to provide such elements which have good speed and contrast. Still other objects will be apparent from the following description of the invention.
- Silver halide crystals when permitted to grow through Ostwald ripening in a pure system, present triangular and hexagonal outlines.
- a protective colloid binder sufficient forces are exerted in the binder to hold the crystals in a rigid position, and any strains set up in this protective media afiect the crystals in that portion of the matrix. Rupture of the bonds at the gelatin-crystal interface frequently results in desensitization. This is particularly true when a p e e of photographic film i sharply bent or kinked.
- the soluble thallous salts are incorporated with an aqueous solution of silver nitrate.
- This solution is added to a water solution of gelatin containing a water-soluble halide, e. g.,' an alkali metal or ammonium halid whereby silver and thallium halides are precipitated in the gelatin.
- a water-soluble halide e. g.,' an alkali metal or ammonium halid whereby silver and thallium halides are precipitated in the gelatin.
- the emulsions are then ripened, set, washed, digested and sensitized, etc., in the conventional manner.
- the water-soluble thallous salts are used in amounts corresponding to 0.005 to 0.05 and preferably 0.01 to 0.02 mol per cent of thallous nitrate based on thesilver nitrate used-in making the silver halide emulsion.
- an amount of such salt to yield thdcorispbr'id ing proper amount of thallium should. beused.
- the amounts of thallium salts just specified are very small and constitute a small fractional part of the amounts prescribed by prior-art investigators for toning, sensitization, fog reduction, etc., and yet give rather surprising and uniqueresults. The small amounts confer an increased contrast to the emulsion and they are markedly less susceptible to desensitization by kinking of "thin layers of the emulsions.
- Thallous nitrate is most active in gelatino silver iodobromide emulsions, and especially those which are dominantly bromide. They confer an increase in both speed and contrast in addition to the decrease in local desensitization du to kinking photographic films bearing such emulsions in the form of thin layers.
- Gelatin silver iodobromide emulsions were prepared with 1.7 mols per cent iodide, 0 and 0.01 mol per cent 'I'1NO3 (based on silver halide) being present in the silver nitrate solution. The precipitation was then made by the addition to 3N ammonium bromide and 0.5N KI solutions. The emulsions were given a ripening, washed, given a digestion to bring them to their maximum light sensitivity, and coated onto a cellulose acetate film base. The following effects on kink susceptibility and sensitometric properties were observed.
- Example II 22 3? Contrast Fog Control emulsion 100 3. 43 11 Emulsion containing .01 mol per- I 7 cent Tl 100 3. 89 13
- Example VI Three iodobromide photosensitive emulsions were prepared by the method of Example I except that one emulsion contained 0.02 mol per cent of thallous nitrate and one emulsion contained 0.02 mol per cent of hexa-thallium sorbitol. Each emulsion was given the usual ripening, wash, and digestion treatments. After coating, the following sensitometric properties were observed.
- Example III After the start of the precipitation with an ammonium bromide and KI solution and ripening. but beforecompletion of the precipitation and ripening. ofone mol of silver iodobromide emulsion in gelatin, 0.0001 mol of thallous nitrate was added in solution form. The finished emulsion; compared toa control emulsion similarly prepared but without thallous nitrate present, possessed-the following properties.
- Emample IV An aqueous solution of TlNOs was added to separate portions of silver nitrate solution before precipitation of a silver iodobromide emulsion in gelatin after the manner set forth in Example-I.
- the emulsions and'one free from TlNO3 were mixed and ripened in the known manner and contained 2.2 mols per cent of AgI. After washing, the emulsion was digested and made orthochromatic by the addition of a pseudocyanine dye.
- TlNOa The quantity of TlNOa is given below along with photographic results.
- Example V g ggg Contrast Fog Standard Emulsion 100 .89 Emulsion containing 02 mol percent TiNOa 93 1.05 .20
- Example VII Silver iodobromide emulsions were. prepared with 0 and 0.02 mol per cent TlNOs based on silver halide. present in the silver nitrate. solution. After precipitation after the manner set forthin Example I and ripening,.the. emulsions were washed, sensitized with 0.12 mg. sodium thiosulfate per kg. of silver halide, treated with 0.27 mg. gold chloride and 0.09 mg. mercuric chloride, digested, brought to their maximum light sensitivity, and coated. The effects observed aretabulated below.
- Example VIII During the initial stages of preparation of one mol of chloro-bromide-gelatin emulsion by precipitation as set forth in Example I, 0.001 mol of thallous nitrate was added. At the same time a similar emulsion without thallous nitrate was The kink susceptibility of the photographic X-ray films described in the foregoing examples was determined as follows: The coated films were kinked in a stainless steel device which had two interfitting parts, each part consisting of a V- shaped groove and an inverted V-shaped projection. The apex of the projections were rounded and one had a radius of curvature of of an inch and the other of an inch. The base of the grooves were 20 mm.
- This tester produced two longitudinal bends in a 35 mm. test strip of film.
- the films were kinked before normal exposure and were then developed in a standard developer, fixed, washed and dried.
- the strips exhibited desensitization at the areas of curvature, and the amount of desensitization was a direct function of the susceptibility of the film to desensitization from handling kinks.
- To assign a numerical value to this susceptibility at the step having a normal net density of 1.0 the ratio of the minimum net density in a klnked area to the normal net density in the same step of the wedge was selected.
- the proportions of thallous salts in mol per cent of the silver nitrate correspond to 0.005 to 0.05 and preferably 0.01 to 0.02 mol per cent of thallium based on the silver present in the emulsions.
- the thallium is probably present in the form of thallous halide.
- the invention is not limited to the specific light-sensitive material described in the above-detailed examples.
- various other simple and mixed silver halides may be used as the light-sensitive materials in like manner.
- Mixtures of silver bromides, chlorides, and/or iodides can be made by adding mixtures of soluble salts of these halides in like manner.
- Other useful soluble halides include potassium bromide, potassium iodide, sodium and potassium chlorides and iodides, etc.
- Other useful soluble silver salts include silver sulfamate, silver sulfate, silver citrate, and silver acetate.
- thallous salts described in the examples one may use the following additional salts: thallous acetate, thallous chlorate, thallous sulfate, thallous cyanide, thallous fluoride, and thallous oxalate.
- This invention is not limited to the use of gelatin as the binding agent for the silver halides.
- other hydrophilic colloids can be used. Suitable colloids include agar-agar, polyglycuronic acids, zein, collodion, water-solubl cellulose derivatives, such as substantially hydrolyzed cellulose acetate, cellulose esters of hydroxy monocarboxylic acids, e.
- lactic or glycolic acids alkali metal salts of cellulose esters of dicarboxylic acids, such as phthalic acid, polyvinyl alcohol, partially hydrolyzed polyvinyl acetate and interpolymers thereof with unsaturated materials, such as styrene, maleic acid, etc., watersoluble polyvinyl acetals and other hydrophilic synthetic or natural resins and polymeric compounds.
- Suitable hydrophilic colloids of the above types are described in United States Patents 2,110,491, 2,276,322, 2,276,323, 2,286,215, and 2,211,323.
- sensitizing agents e. g., sulfur sensitizers, such as allylthioureas, thiocyanates, or allylthiocyanates
- sulfur sensitizers such as allylthioureas, thiocyanates, or allylthiocyanates
- optical sensitizing dyes which modify the spectral characteristics of the resulting emulsions can be added. Suitable sensitizing dyes are described in United States Patents 2,010,388, 2,079,376, 2,202,990, 2,202,991, 2,202,992, 2,278,461, 2,265,908, etc.
- An advantage of the invention is that it provides a simple and effective method for increasing the contrast of photographic silver halide emulsions. Another advantage is that it provides an effective and economical method for reducing the kink susceptibility of photographic films. This is important in large sheets of X-ray and portrait film. In the former, the markings may lead to confusion in the interpretation of radiographs.
- a method of making a colloid silver halide emulsion which comprises adding to an aqueous colloid solution a water-soluble silver salt and a water-soluble thallous salt, precipitating silver and thallous halides, ripending the resulting emulsion and preparing the ripened emulsion for coating, said water-soluble thallous salt being used in an amount of 0.005 to 0.05 mol per cent based on the water-soluble silver salt.
- a method of making a light-sensitive colloid silver halide emulsion which comprises adding to an aqueous water-permeable colloid solution containing at least one water-soluble inorganic halide, a water-soluble silver salt and a watersoluble thallous salt to precipitate silver and thallous halides in said colloid, ripening the resulting emulsion and preparing the ripened emulsion for coating, said water-soluble thallous salt being used in an amount of 0.005 to 0.05 mol per cent based on the water-soluble silver salt.
- a method of making a light-sensitive gelatino silver halide emulsion which comprises adding to an aqueous gelatin solution containing at least one water-soluble inorganic halide an aqueous solution of a water-soluble silver salt and a water-soluble thallous salt to precipitate silver and thallous halides in the gelatin, ripening the resulting gelatin emulsion and preparing the ripened emulsion for coating, said water-soluble thallous salt being present in an amount of 0.005 to 0.05 mol per cent based on the water-soluble silver salt.
- a method of making a light-sensitive gelatino silver halide emulsion which comprises adding to an aqueous gelatin solution containing ammonium bromide and potassium iodide, an aqueous solution of a water-soluble silver salt and a water-soluble thallous salt to precipitate silver and thallous halides in the gelatin, ripening the resulting gelatin emulsion and preparing the ripened emulsion for coating, said water-soluble thallous salt being present in an amount of 0.005 to 0.05 mol per cent based on the water-soluble silver salt.
- a method of making a colloid silver halide emulsion which comprises adding to an aqueous colloid solution containing a water-soluble inorganic halide silver nitrate and thallous nitrate in an amount of 0.005 to 0.05 mol per cent based on silver nitrate, to precipitate silver and thallous halides, ripening the resulting emulsion and preparing the resulting emulsion for coating.
- a method of making a light-sensitive gelatin silver halide emulsion which comprises adding to an aqueous solution of gelatin containing at least one water-soluble inorganic halide an aqueous solution of silver nitrate and thallous nitrate in an amount of 0.005 to 0.05 mol per cent based on silver nitrate to precipitate silver and thallous halides, ripening the resulting emulsion and preparing the resulting emulsion for coating.
- a method of making a light-sensitive gelatino silver halide emulsion which comprises adding to an aqueous solution of gelatin containing ammonium bromide and potassium iodide an 7 aqueous solution of silver nitrateand thallous nitrate in an amount of 0.005 to 0.05 mol per cent based on silver nitrate, to precipitate silver and thallous halides, ripening the resulting emulsion and preparing said emulsion for coating.
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- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Description
Patented Feb. 10, 1953 METHOD OF MAKING COLLOID SILVER HAL- IDE EMULSION S CONTAINING THALLIUM Joseph De Witt Overman, Milltown, N. J assignor to E. I. do Pont de Nemours & Company, Wilmington, Del., a corporation of Delaware No Drawing.
Application April 29, 1948,
Serial No. 24,102
'7 Claims.
This invention relates to photographic elements, to light-sensitive silver halide emulsions and to their preparation. More particularly it relates to photographic elements bearing a colloid silver halide emulsion layer which contains a small amount of thallium.
An object of this invention is to provide photographic silver halide emulsion layers which are more resistant to local desensitization due to abrasive forces. A related object is to provide flexible photographic elements with silver halide emulsion layers which are more resistant to desensitization due to kinking. A further object is to provide such elements which have good speed and contrast. Still other objects will be apparent from the following description of the invention.
Various metal salts have been added to silver halide emulsions for various purposes including toning of the developed silver image, reducing fog, increasing sensitivity, etc. Among such salts are the salts of thallium. However, the amounts proposed are quite different from those comprehended by the present invention.
It has been found that if very small amounts of thallous salts are present during the formation and growth of silver halide crystals in a colloidal system, the resulting emulsions have increased contrast and good speed. Thin emulsion layers made from such emulsions have a quite marked decrease in local desensitization caused by abrasive forces or kinking of the layers.
Silver halide crystals, when permitted to grow through Ostwald ripening in a pure system, present triangular and hexagonal outlines. In a sysitem using a protective colloid binder, sufficient forces are exerted in the binder to hold the crystals in a rigid position, and any strains set up in this protective media afiect the crystals in that portion of the matrix. Rupture of the bonds at the gelatin-crystal interface frequently results in desensitization. This is particularly true when a p e e of photographic film i sharply bent or kinked.
The incorporation of small amounts of watersoluble thallium salts in the silver halide crystal distorts the lattice so that during the Ostwald ripening the normal habit of the crystal is no longer discernible under a microscope of 430x magnification, and the crystal appears to be more nearly spherical in shape. These more nearly spherical grains are held by the protective colloid with forces equal to that encountered with the hexagonal grains, but are less affected by bends or kinks in films containing them.
The soluble thallous salts are incorporated with an aqueous solution of silver nitrate. This solution is added to a water solution of gelatin containing a water-soluble halide, e. g.,' an alkali metal or ammonium halid whereby silver and thallium halides are precipitated in the gelatin. The emulsions are then ripened, set, washed, digested and sensitized, etc., in the conventional manner.
The water-soluble thallous salts are used in amounts corresponding to 0.005 to 0.05 and preferably 0.01 to 0.02 mol per cent of thallous nitrate based on thesilver nitrate used-in making the silver halide emulsion. When salts other than thallous nitrate and silver nitrate are used, an amount of such salt to yield thdcorispbr'id ing proper amount of thallium should. beused. The amounts of thallium salts just specified are very small and constitute a small fractional part of the amounts prescribed by prior-art investigators for toning, sensitization, fog reduction, etc., and yet give rather surprising and uniqueresults. The small amounts confer an increased contrast to the emulsion and they are markedly less susceptible to desensitization by kinking of "thin layers of the emulsions. V 1
Thallous nitrate is most active in gelatino silver iodobromide emulsions, and especially those which are dominantly bromide. They confer an increase in both speed and contrast in addition to the decrease in local desensitization du to kinking photographic films bearing such emulsions in the form of thin layers.
The invention will be further described but is not intended to be limited by the following examples. The operations are carried out in the absence of actinic light. H
Example] y:
Gelatin silver iodobromide emulsions were prepared with 1.7 mols per cent iodide, 0 and 0.01 mol per cent 'I'1NO3 (based on silver halide) being present in the silver nitrate solution. The precipitation was then made by the addition to 3N ammonium bromide and 0.5N KI solutions. The emulsions were given a ripening, washed, given a digestion to bring them to their maximum light sensitivity, and coated onto a cellulose acetate film base. The following effects on kink susceptibility and sensitometric properties were observed.
Kink Mol Percent TlNOs jggg Contrast Suscepti iv.
Example II 22 3? Contrast Fog Control emulsion 100 3. 43 11 Emulsion containing .01 mol per- I 7 cent Tl 100 3. 89 13 Example VI Three iodobromide photosensitive emulsions were prepared by the method of Example I except that one emulsion contained 0.02 mol per cent of thallous nitrate and one emulsion contained 0.02 mol per cent of hexa-thallium sorbitol. Each emulsion was given the usual ripening, wash, and digestion treatments. After coating, the following sensitometric properties were observed.
Kink Relative Contrast Suscepti- Speed bility Control Emulsion 100 3.18 .66 Emulsion containing .02 mol percent TlNOa 114 3. 33 .75 Emulsion containing 0.02 mol percent TIBCBHBOs 114 3.36 .85
Example III After the start of the precipitation with an ammonium bromide and KI solution and ripening. but beforecompletion of the precipitation and ripening. ofone mol of silver iodobromide emulsion in gelatin, 0.0001 mol of thallous nitrate was added in solution form. The finished emulsion; compared toa control emulsion similarly prepared but without thallous nitrate present, possessed-the following properties.
Film 322? Contrast Fog Control.....-... 100 2.93 .08 Emulsion containing .01 mol percent lhallous Nitrate as a" separate solution 126 2. 96
Emample IV An aqueous solution of TlNOs was added to separate portions of silver nitrate solution before precipitation of a silver iodobromide emulsion in gelatin after the manner set forth in Example-I. The emulsions and'one free from TlNO3 were mixed and ripened in the known manner and contained 2.2 mols per cent of AgI. After washing, the emulsion was digested and made orthochromatic by the addition of a pseudocyanine dye.
The quantity of TlNOa is given below along with photographic results.
' MOIsAgNm Mols TING gg Control Fog 1.0 comer 100 1.77 .11 1,0, 010..... 130 1.9 .14 1.0. ooozo 145 2.21 .18
Example V g ggg Contrast Fog Standard Emulsion 100 .89 Emulsion containing 02 mol percent TiNOa 93 1.05 .20
Example VII Silver iodobromide emulsions were. prepared with 0 and 0.02 mol per cent TlNOs based on silver halide. present in the silver nitrate. solution. After precipitation after the manner set forthin Example I and ripening,.the. emulsions were washed, sensitized with 0.12 mg. sodium thiosulfate per kg. of silver halide, treated with 0.27 mg. gold chloride and 0.09 mg. mercuric chloride, digested, brought to their maximum light sensitivity, and coated. The effects observed aretabulated below.
Relative Film speed Contrast Fog Without thallous nitrate 2. 51 02 With thallous nitrate 2; 53 .02
Example VIII During the initial stages of preparation of one mol of chloro-bromide-gelatin emulsion by precipitation as set forth in Example I, 0.001 mol of thallous nitrate was added. At the same time a similar emulsion without thallous nitrate was The kink susceptibility of the photographic X-ray films described in the foregoing examples was determined as follows: The coated films were kinked in a stainless steel device which had two interfitting parts, each part consisting of a V- shaped groove and an inverted V-shaped projection. The apex of the projections were rounded and one had a radius of curvature of of an inch and the other of an inch. The base of the grooves were 20 mm. wide and the depth of the grooves 10 mm. This tester produced two longitudinal bends in a 35 mm. test strip of film. The films were kinked before normal exposure and were then developed in a standard developer, fixed, washed and dried. The strips exhibited desensitization at the areas of curvature, and the amount of desensitization was a direct function of the susceptibility of the film to desensitization from handling kinks. To assign a numerical value to this susceptibility at the step having a normal net density of 1.0, the ratio of the minimum net density in a klnked area to the normal net density in the same step of the wedge was selected.
The six-inch 35 mm. X-ray film strips were exposed in contact with a barium-calcium tungstate X-ray intensifying screen which fiuoresces chiefly in the blue region of the spectrum. It was excited by radiation from a General Electric KX-B Model X-ray machine at 70 kvp., 150 ma. for second at 64 inches through a 1.5 mm. aluminum filter, using an XP4.5 tube. Development was for 4 minutes at 68 in a metol-hydroquinone developer. Fixation was for minutes in a thiosulfate fixer containing chrome alum as a hardener. Densities were determined on a stroboscopic photoelectric densitometer (J. Soc. Mot. Picture Engrs., 33, 403 (1939)).
The proportions of thallous salts in mol per cent of the silver nitrate correspond to 0.005 to 0.05 and preferably 0.01 to 0.02 mol per cent of thallium based on the silver present in the emulsions. The thallium is probably present in the form of thallous halide.
The invention, moreover, is not limited to the specific light-sensitive material described in the above-detailed examples. On the contrary, various other simple and mixed silver halides may be used as the light-sensitive materials in like manner. Mixtures of silver bromides, chlorides, and/or iodides can be made by adding mixtures of soluble salts of these halides in like manner. Other useful soluble halides include potassium bromide, potassium iodide, sodium and potassium chlorides and iodides, etc. Other useful soluble silver salts include silver sulfamate, silver sulfate, silver citrate, and silver acetate. Similarly, in place of the thallous salts described in the examples one may use the following additional salts: thallous acetate, thallous chlorate, thallous sulfate, thallous cyanide, thallous fluoride, and thallous oxalate.
This invention is not limited to the use of gelatin as the binding agent for the silver halides. On the contrary, other hydrophilic colloids can be used. Suitable colloids include agar-agar, polyglycuronic acids, zein, collodion, water-solubl cellulose derivatives, such as substantially hydrolyzed cellulose acetate, cellulose esters of hydroxy monocarboxylic acids, e. g., lactic or glycolic acids, alkali metal salts of cellulose esters of dicarboxylic acids, such as phthalic acid, polyvinyl alcohol, partially hydrolyzed polyvinyl acetate and interpolymers thereof with unsaturated materials, such as styrene, maleic acid, etc., watersoluble polyvinyl acetals and other hydrophilic synthetic or natural resins and polymeric compounds. Suitable hydrophilic colloids of the above types are described in United States Patents 2,110,491, 2,276,322, 2,276,323, 2,286,215, and 2,211,323.
During the digestion Stage or prior thereto, various types of sensitizing agents, e. g., sulfur sensitizers, such as allylthioureas, thiocyanates, or allylthiocyanates, can be used. In addition, various types of optical sensitizing dyes which modify the spectral characteristics of the resulting emulsions can be added. Suitable sensitizing dyes are described in United States Patents 2,010,388, 2,079,376, 2,202,990, 2,202,991, 2,202,992, 2,278,461, 2,265,908, etc.
An advantage of the invention is that it provides a simple and effective method for increasing the contrast of photographic silver halide emulsions. Another advantage is that it provides an effective and economical method for reducing the kink susceptibility of photographic films. This is important in large sheets of X-ray and portrait film. In the former, the markings may lead to confusion in the interpretation of radiographs.
As many widely different embodiments of this invention can be made without departing from th spirit and scope thereof, it is to be understood that the invention is not to be limited except as defined by the claims.
What is claimed is:
1. A method of making a colloid silver halide emulsion which comprises adding to an aqueous colloid solution a water-soluble silver salt and a water-soluble thallous salt, precipitating silver and thallous halides, ripending the resulting emulsion and preparing the ripened emulsion for coating, said water-soluble thallous salt being used in an amount of 0.005 to 0.05 mol per cent based on the water-soluble silver salt.
2. A method of making a light-sensitive colloid silver halide emulsion which comprises adding to an aqueous water-permeable colloid solution containing at least one water-soluble inorganic halide, a water-soluble silver salt and a watersoluble thallous salt to precipitate silver and thallous halides in said colloid, ripening the resulting emulsion and preparing the ripened emulsion for coating, said water-soluble thallous salt being used in an amount of 0.005 to 0.05 mol per cent based on the water-soluble silver salt.
3. A method of making a light-sensitive gelatino silver halide emulsion which comprises adding to an aqueous gelatin solution containing at least one water-soluble inorganic halide an aqueous solution of a water-soluble silver salt and a water-soluble thallous salt to precipitate silver and thallous halides in the gelatin, ripening the resulting gelatin emulsion and preparing the ripened emulsion for coating, said water-soluble thallous salt being present in an amount of 0.005 to 0.05 mol per cent based on the water-soluble silver salt.
4. A method of making a light-sensitive gelatino silver halide emulsion which comprises adding to an aqueous gelatin solution containing ammonium bromide and potassium iodide, an aqueous solution of a water-soluble silver salt and a water-soluble thallous salt to precipitate silver and thallous halides in the gelatin, ripening the resulting gelatin emulsion and preparing the ripened emulsion for coating, said water-soluble thallous salt being present in an amount of 0.005 to 0.05 mol per cent based on the water-soluble silver salt.
5. A method of making a colloid silver halide emulsion which comprises adding to an aqueous colloid solution containing a water-soluble inorganic halide silver nitrate and thallous nitrate in an amount of 0.005 to 0.05 mol per cent based on silver nitrate, to precipitate silver and thallous halides, ripening the resulting emulsion and preparing the resulting emulsion for coating.
6. A method of making a light-sensitive gelatin silver halide emulsion which comprises adding to an aqueous solution of gelatin containing at least one water-soluble inorganic halide an aqueous solution of silver nitrate and thallous nitrate in an amount of 0.005 to 0.05 mol per cent based on silver nitrate to precipitate silver and thallous halides, ripening the resulting emulsion and preparing the resulting emulsion for coating.
7. A method of making a light-sensitive gelatino silver halide emulsion which comprises adding to an aqueous solution of gelatin containing ammonium bromide and potassium iodide an 7 aqueous solution of silver nitrateand thallous nitrate in an amount of 0.005 to 0.05 mol per cent based on silver nitrate, to precipitate silver and thallous halides, ripening the resulting emulsion and preparing said emulsion for coating.
JOSEPH DE WITT OVERMAN.
REFERENCES CITED The following references are of record in the file of this patent:
8 UNITED STATES, PATENTS Number Number
Claims (1)
1. A METHOD OF MAKING A COLLOID SILVER HALIDE EMULSION WHICH COMPRISES ADDING TO AN AQUEOUS COLLOID SOLUTION A WATER-SOLUBLE SILVER SALT AND A WATER-SOLUBLE THALLOUS SALT, PRECIPITATING SILVER AND THALLOUSE HALIDES, RIPENDING THE RESULTING EMULSION AND PREPARING THE RIPENED EMULSION FOR COATEING, SAID WATER-SOLUBLE THALLOUSE SALT BEING USED IN AN AMOUNT OF 0.005 TO 0.05 MOL PER CENT BASED ON THE WATER-SOLUBLE SILVER SALT.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
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US24102A US2628167A (en) | 1948-04-29 | 1948-04-29 | Method of making colloid silver halide emulsions containing thallium |
GB11211/49A GB658434A (en) | 1948-04-29 | 1949-04-27 | Improvements in or relating to light-sensitive silver halide emulsions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US24102A US2628167A (en) | 1948-04-29 | 1948-04-29 | Method of making colloid silver halide emulsions containing thallium |
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US2628167A true US2628167A (en) | 1953-02-10 |
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US24102A Expired - Lifetime US2628167A (en) | 1948-04-29 | 1948-04-29 | Method of making colloid silver halide emulsions containing thallium |
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GB (1) | GB658434A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3201255A (en) * | 1959-08-19 | 1965-08-17 | Gen Aniline & Film Corp | Photopolymerization of vinyl monomers by means of thallium compounds as catalysts |
US3852067A (en) * | 1971-11-04 | 1974-12-03 | Polaroid Corp | Photosensitive element with silver halide, a semiconductor and a sensitizing dye |
US3852066A (en) * | 1971-11-04 | 1974-12-03 | Polaroid Corp | Silver halide with an orthorhombic lead monoxide and sensitizing dye |
US4013469A (en) * | 1974-07-05 | 1977-03-22 | Teruhide Haga | Chemical development of a silver halide emulsion containing an arylonium salt on a polyester film support |
EP0198634A2 (en) | 1985-04-04 | 1986-10-22 | EASTMAN KODAK COMPANY (a New Jersey corporation) | Quaternized tellurium salt fog inhibiting agents for silver halide photography |
EP0239363A2 (en) | 1986-03-25 | 1987-09-30 | Konica Corporation | Light-sensitive silver halide photographic material feasible for high speed processing |
US4826758A (en) * | 1986-04-19 | 1989-05-02 | Konishiroku Photo Industry Co., Ltd. | Silver halide emulsion and process for preparing it, and light-sensitive halide photographic material employing said silver halide emulsion |
USH874H (en) * | 1986-06-04 | 1991-01-01 | Konishiroku Photo Industry Co., Ltd. | Process for manufacturing a silver halide photographic material having a support and at least one hydrophilic colloid layer |
EP0699944A1 (en) | 1994-08-26 | 1996-03-06 | Eastman Kodak Company | Tabular grain emulsions with sensitization enhancements |
EP0699946A1 (en) | 1994-08-26 | 1996-03-06 | Eastman Kodak Company | Ultrathin tabular grain emulsions with sensitization enhancements (II) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3620750A (en) * | 1969-01-09 | 1971-11-16 | Agfa Gevaert Ag | Direct positive silver halide emulsions containing thallium salt and mercury salt |
CN115506062B (en) * | 2022-10-21 | 2024-09-06 | 石狮市益明染织有限公司 | Environment-friendly flame-retardant polyester yarn and preparation method thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE428898C (en) * | 1925-11-13 | 1926-05-12 | Robert Schwarz Dr | Process for sensitizing photographic silver halide layers to X-rays |
US2105274A (en) * | 1935-12-13 | 1938-01-11 | Felix Sager & Dr Gossler Gmbh | Process of preventing yellow stain in photographic preparations and regulation of the halogen content thereof |
US2432865A (en) * | 1944-02-03 | 1947-12-16 | Ilford Ltd | Photographic elements having light-sensitive silver halide layers containing iron, cobalt and nickel derivatives of mercapto tetrazoles, triazoles or diazoles |
-
1948
- 1948-04-29 US US24102A patent/US2628167A/en not_active Expired - Lifetime
-
1949
- 1949-04-27 GB GB11211/49A patent/GB658434A/en not_active Expired
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE428898C (en) * | 1925-11-13 | 1926-05-12 | Robert Schwarz Dr | Process for sensitizing photographic silver halide layers to X-rays |
US2105274A (en) * | 1935-12-13 | 1938-01-11 | Felix Sager & Dr Gossler Gmbh | Process of preventing yellow stain in photographic preparations and regulation of the halogen content thereof |
US2432865A (en) * | 1944-02-03 | 1947-12-16 | Ilford Ltd | Photographic elements having light-sensitive silver halide layers containing iron, cobalt and nickel derivatives of mercapto tetrazoles, triazoles or diazoles |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3201255A (en) * | 1959-08-19 | 1965-08-17 | Gen Aniline & Film Corp | Photopolymerization of vinyl monomers by means of thallium compounds as catalysts |
US3852067A (en) * | 1971-11-04 | 1974-12-03 | Polaroid Corp | Photosensitive element with silver halide, a semiconductor and a sensitizing dye |
US3852066A (en) * | 1971-11-04 | 1974-12-03 | Polaroid Corp | Silver halide with an orthorhombic lead monoxide and sensitizing dye |
US4013469A (en) * | 1974-07-05 | 1977-03-22 | Teruhide Haga | Chemical development of a silver halide emulsion containing an arylonium salt on a polyester film support |
EP0198634A2 (en) | 1985-04-04 | 1986-10-22 | EASTMAN KODAK COMPANY (a New Jersey corporation) | Quaternized tellurium salt fog inhibiting agents for silver halide photography |
EP0239363A2 (en) | 1986-03-25 | 1987-09-30 | Konica Corporation | Light-sensitive silver halide photographic material feasible for high speed processing |
US4826758A (en) * | 1986-04-19 | 1989-05-02 | Konishiroku Photo Industry Co., Ltd. | Silver halide emulsion and process for preparing it, and light-sensitive halide photographic material employing said silver halide emulsion |
USH874H (en) * | 1986-06-04 | 1991-01-01 | Konishiroku Photo Industry Co., Ltd. | Process for manufacturing a silver halide photographic material having a support and at least one hydrophilic colloid layer |
EP0699944A1 (en) | 1994-08-26 | 1996-03-06 | Eastman Kodak Company | Tabular grain emulsions with sensitization enhancements |
EP0699946A1 (en) | 1994-08-26 | 1996-03-06 | Eastman Kodak Company | Ultrathin tabular grain emulsions with sensitization enhancements (II) |
Also Published As
Publication number | Publication date |
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GB658434A (en) | 1951-10-10 |
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