US3649286A - Process for spectrally sensitizing photographic silver halide emulsions - Google Patents
Process for spectrally sensitizing photographic silver halide emulsions Download PDFInfo
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- US3649286A US3649286A US761841A US3649286DA US3649286A US 3649286 A US3649286 A US 3649286A US 761841 A US761841 A US 761841A US 3649286D A US3649286D A US 3649286DA US 3649286 A US3649286 A US 3649286A
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- dye
- silver halide
- silica particles
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- silica
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- 239000000839 emulsion Substances 0.000 title claims abstract description 59
- -1 silver halide Chemical class 0.000 title claims abstract description 58
- 229910052709 silver Inorganic materials 0.000 title claims abstract description 52
- 239000004332 silver Substances 0.000 title claims abstract description 52
- 238000000034 method Methods 0.000 title claims abstract description 44
- 230000001235 sensitizing effect Effects 0.000 title claims abstract description 36
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 92
- 230000003595 spectral effect Effects 0.000 claims abstract description 15
- 239000007788 liquid Substances 0.000 claims abstract description 7
- 239000000377 silicon dioxide Substances 0.000 claims description 24
- 239000003960 organic solvent Substances 0.000 claims description 13
- 239000008119 colloidal silica Substances 0.000 claims description 9
- 108010010803 Gelatin Proteins 0.000 claims description 6
- 239000008273 gelatin Substances 0.000 claims description 6
- 229920000159 gelatin Polymers 0.000 claims description 6
- 235000019322 gelatine Nutrition 0.000 claims description 6
- 235000011852 gelatine desserts Nutrition 0.000 claims description 6
- DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 claims description 4
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims description 4
- 238000012546 transfer Methods 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 2
- 239000000975 dye Substances 0.000 description 56
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000035945 sensitivity Effects 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000004848 polyfunctional curative Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 229920002301 cellulose acetate Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- LUMLZKVIXLWTCI-NSCUHMNNSA-N (e)-2,3-dichloro-4-oxobut-2-enoic acid Chemical compound OC(=O)C(\Cl)=C(/Cl)C=O LUMLZKVIXLWTCI-NSCUHMNNSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- KRTDQDCPEZRVGC-UHFFFAOYSA-N 2-nitro-1h-benzimidazole Chemical compound C1=CC=C2NC([N+](=O)[O-])=NC2=C1 KRTDQDCPEZRVGC-UHFFFAOYSA-N 0.000 description 1
- VYDWQPKRHOGLPA-UHFFFAOYSA-N 5-nitroimidazole Chemical compound [O-][N+](=O)C1=CN=CN1 VYDWQPKRHOGLPA-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000206672 Gelidium Species 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- LEVWYRKDKASIDU-IMJSIDKUSA-N L-cystine Chemical compound [O-]C(=O)[C@@H]([NH3+])CSSC[C@H]([NH3+])C([O-])=O LEVWYRKDKASIDU-IMJSIDKUSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
- HOLVRJRSWZOAJU-UHFFFAOYSA-N [Ag].ICl Chemical compound [Ag].ICl HOLVRJRSWZOAJU-UHFFFAOYSA-N 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000010419 agar Nutrition 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 235000016720 allyl isothiocyanate Nutrition 0.000 description 1
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
- 229910001864 baryta Inorganic materials 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- 239000000298 carbocyanine Substances 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 229960003067 cystine Drugs 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000000326 densiometry Methods 0.000 description 1
- 150000002012 dioxanes Chemical class 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002344 gold compounds Chemical class 0.000 description 1
- RJHLTVSLYWWTEF-UHFFFAOYSA-K gold trichloride Chemical compound Cl[Au](Cl)Cl RJHLTVSLYWWTEF-UHFFFAOYSA-K 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- ZAKLKBFCSHJIRI-UHFFFAOYSA-N mucochloric acid Natural products OC1OC(=O)C(Cl)=C1Cl ZAKLKBFCSHJIRI-UHFFFAOYSA-N 0.000 description 1
- 150000002941 palladium compounds Chemical class 0.000 description 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- QWYZFXLSWMXLDM-UHFFFAOYSA-M pinacyanol iodide Chemical class [I-].C1=CC2=CC=CC=C2N(CC)C1=CC=CC1=CC=C(C=CC=C2)C2=[N+]1CC QWYZFXLSWMXLDM-UHFFFAOYSA-M 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical class O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 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
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical group C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 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
- G03C1/08—Sensitivity-increasing substances
- G03C1/10—Organic substances
- G03C1/102—Organic substances dyes other than methine dyes
Definitions
- ABSTRACT A process for spectrally sensitizing photographic silver halide which comprises: adsorbing a photographic spectral sensitizing dye onto finely divided silica particles; and adding the dyed silica particles to a liquid photographic silver halide emulsion.
- the conventional method of sensitizing silver halide emulsions consists of dissolving the sensitizing dye in an appropriate organic solvent such as methyl alcohol, ethyl alcohol, acetone, etc., and adding the resulting solution to the liquid emulsion. While this general method has provided a commercially feasible means for incorporating sensitizing dyes into silver halide emulsions, it introduces undesirable amounts of organic solvent into the emulsion, which can result in coating defects or wandering of the dye in various layers of a photographic element.
- an appropriate organic solvent such as methyl alcohol, ethyl alcohol, acetone, etc.
- an object of this invention to provide a new and improved method for incorporating sensitizing dyes into photographic silver halide emulsions.
- Another object of this invention is to provide an efficient, readily controllable means for incorporating sensitizing dyes into such emulsions.
- Another object is to provide novel silver halide emulsions and elements.
- silica finely divided silica
- the spectral sensitizing dye transfers to the silver halide crystals, and becomes effectively adsorbed thereto. This results in spectral sensitization of the silver halide grains in the emulsion.
- the silica remains in photographic layers produced with emulsions prepared in accordance with this invention. The residual silica in the layers inhibits dye wandering and provides tooth which facilitates retouching or writing thereon.
- the method of this invention fully overcomes the mentioned shortcomings of the prior art procedures.
- the need of using organic solvents in the prior art processes to incorporate the dyes into the emulsions is completely eliminated in the method ofthis invention.
- Suitable silicas for practicing this invention include silicon dioxide particles having an average diameter ranging from about 0.001 to microns.
- Useful materials of this kind are commercially available under various trade names, e.g., Cabo-Sil, a colloidal silica manufactured by Godfrey L. Cabot, lnc.; Celite, a diatomaceous silica manufactured by John- Manville Sales Corp.; Nalcosil, a colloidal silica manufactured by Nalco Chem. Co.; Hi-Sil, an ultra-fine silica manufactured by Pittsburgh Plate Glass Co.; Si-O-Lite, fine silica manufactured by Mallinkrodt Chem. Co.; powdered silica gels and the like.
- concentration of the silica which is most advantageously employed will depend, of course upon the silver halide emulsion employed and upon the sensitizing dye employed. Ordinarily, however, from about 10 to 150 g., but preferably from about to 50 g., of the silica per gram-mole of silver halide is advantageously used.
- Suitable spectral sensitizing dyes for practicing the invention include any of those known to sensitize silver halide emulsions.
- Typical useful dyes include any of the methine dyes, such as the cyanine dyes (including the carbocyanines, the dicarbocyanines and complex cyanines); merocyanine dyes (including complex merocyanine dyes) and, styryl dyes.
- Typical dyes which can be used in the practice of this invention include any of those disclosed in the following patents, the disclosure of which is incorporated herein by reference.
- the spectral sensitizing dye can be adsorbed to the silica in any convenient manner.
- a spectral sensitizing dye is dissolved in an organic solvent for the dye, and the silica is mixed therewith. After the dye has become adsorbed to the silica, the organic solvent is advantageously removed in any convenient manner. Removal of the organic solvent is not essential to the practice of this invention; however, removal of the organic solvent is the preferred mode of carrying out the invention. Solvent removal can be accomplished in any convenient manner, e.g., by evaporation, filtration or centrifugmg.
- the concentration of the sensitizing dye can with advantage range from about 0.001 to 0.200 g. per gram-mole ofsilver ha lide in the emulsion.
- the dye-containing silica particles are incorporated in the photographic silver halide emulsions at temperatures ranging about from 40 to 60 C.
- the process of this invention is useful in spectrally sensitizing any of the photographic silver halides, including silver bromide, silver chloride, silver bromoiodide, silver chlorobromide, silver chloroiodide or silver chlorobromoiodide.
- the photographic grains can be dispersed in any suitable binder, including such hydrophilic binders as gelatin, albumin, agaragar, gum arabic, alginic acid, polyvinyl alcohol, polyvinyl pyrrolidone, cellulose ethers, partially hydrolyzed cellulose acetate, and the like.
- the binding agents for the emulsion layer of the photographic element can also contain dispersed polymerized vinyl compounds. Such compounds are disclosed, for example, in U. S. Pat. Nos.
- 3,142,568; 3,193,386; 3,062,674 and 3,220,844 and include the water insoluble polymers of alkyl acrylates and methacrylates, acrylic acid, sulfoalkyl acrylates or methacrylates and the like.
- Emulsions sensitized as described herein can be coated on any suitable photographic support, such as glass, film base such as cellulose acetate, cellulose acetate butyrate, polyesters such as poly(ethylene terephthalate), paper, baryta coated paper, polyolefin coated paper, e.g., polyethylene or polypropylene coated paper, which may be electron bombarded to promote emulsion adhesion, to produce the novel photographic elements of the invention.
- film base such as cellulose acetate, cellulose acetate butyrate
- polyesters such as poly(ethylene terephthalate), paper, baryta coated paper, polyolefin coated paper, e.g., polyethylene or polypropylene coated paper, which may be electron bombarded to promote emulsion adhesion, to produce the novel photographic elements of the invention.
- Emulsions sensitized in accordance with this invention can contain addenda such as chemical sensitizers, e.g., sulfur sensitizers (e.g., allyl thiocarbamate, thiourea, allyl-isothiocyanate, cystine, etcv) various gold compounds (e.g., potassium chloroaurate, auric trichloride, etc. (see Baldsiefen, U.S. Pat. No. 2,540,085, issued Feb. 6, 1951, Damschroder, U.S. Pat. No. 2,597,856, issued May 27, 1952 and Yutzy et al. U.S. Pat. No.
- additiveenda such as chemical sensitizers, e.g., sulfur sensitizers (e.g., allyl thiocarbamate, thiourea, allyl-isothiocyanate, cystine, etcv) various gold compounds (e.g., potassium chloroaurate, auric trichloride,
- the silver halide emulsions of the invention can be hardened with any suitable hardener, including aldehyde hardeners such as formaldehyde, and mucochloric acid, aziridine hardeners, hardeners which are derivatives of dioxane, oxypolysaccharides such as oxy starch or oxy plant gums, and the like.
- aldehyde hardeners such as formaldehyde, and mucochloric acid
- aziridine hardeners hardeners which are derivatives of dioxane, oxypolysaccharides such as oxy starch or oxy plant gums, and the like.
- the emulsion layers can also contain additional additives, particularly those known to be beneficial in photographic emulsions, including, for example, lubricating materials, stabilizers speed increasing materials, absorbing dyes, plasticizers, and the like. These photographic emulsions can also contain in some cases additional spectral sensitizing dyes. Furthermore, these emulsions can contain color-forming couplers or can be developed in solutions containing couplers or other color generating materials.
- the useful color formers are the monomeric and polymeric color formers, e.g., pyrazolone color formers, as well as phenolic, heterocyclic and open chain couplers having a reactive methylene group.
- the color-forming couplers can be incorporated into the photographic silver halide emulsion using any suitable technique, e.g., techniques of the type shown in Jelley et a1.
- U.S. Pat. No. 2,322,027 issued June 15, 1943, Fierke et a1.
- U.S. Pat. No. 2,801,171, issued July 30, 1957 Fisher U.S. Pat. Nos. 1,055,155 and 1,102,028, issued Mar. 4, 1913 and June 30, 1914, respectively, and Wilmanns U.S. Pat. No. 2,186,849, issued Jan. 9, 1949.
- They can also be developed using incorporated developers such as polyhydroxybenzenes, aminophenols, 3-pyrazolidones, and the like.
- each solution is then added to 1.0 g. of finely divided silica (Cab-O-sil, a trade name for colloidal silica manufactured by Godfrey L Cabot, lnc.).
- Cab-O-sil a trade name for colloidal silica manufactured by Godfrey L Cabot, lnc.
- Each mixture is centrifuged to separate the dyes silica from the solvent.
- the samples of dyed silica are in each case dried and powdered.
- the ratio of dye to silica will vary depending on the starting dye concentration, on the absorbing time, etc. These conditions can be adjusted in each case to produce a dye concentration giving the optimum sensitizing results.
- the dyed silica in each instance is then added directly to a stirred aqueous gelatin silver bromoiodide emulsion at 40 C.
- N-rnethyl-p-aminophenol sulfate 2.0 g. Hydroquinone 8.0 g. Sodium sulfite (desiccated) 90.0 g. Sodium carbonate lmonohydrate) 52.5 5. Potassium bromide 5.0 g.
- Coating contained 1.66 g. 01 Loucophor Blmole of silver is stilbene type of brightening agent; colour index, 2nd edition, vol. 2, p. 2914).
- a process for spectrally sensitizing photographic silver halide which comprises: adsorbing a photographic spectral sensitizing dye onto finely divided silica particles; and, adding the dyed silica particles to a liquid photographic silver halide emulsion to transfer dye from the silica particles to the silver halide grains in said emulsion.
- silica particles have an average diameter of from about 0.001 to 10 microns.
- the photographic silver halide emulsion is an aqueous gelatin silver halide emulsion.
- said spectral sensitizing dye is selected from the group consisting of a cyanine dye and a merocyanine dye.
- a process for spectrally sensitizing photographic silver halide which comprises: dissolving a photographic spectral sensitizing dye in an organic solvent; mixing finely divided silica particles with a solution of dye in organic solvent to adsorb the dye onto the silica particles; removing the organic solvent; and, adding the dyed silica particles to a liquid photographic silver halide emulsion to transfer dye from the silica particles to the silver halide grains in said emulsion.
- silica particles have an average diameter of from about 0.001 to microns.
- silica particles comprise colloidal silica and said dye is a 1,1- diethyl-2,2-cyanine salt.
- silica particles comprise colloidal silica and said dye is anhydro- 5,5,6,6 1,! '-diethyl-3,3'-di(3-sulfobutyl)- benzimidazolocarbocyanine hydroxide.
- silica particles comprise colloidal silica and said dye is 3-( 3- dimethylaminopropyl )-5- -2-thio-2,4-oxazolidinedione.
- a photographic element comprising a support having thereon a layer containing a photographic silver halide emulsion prepared by the process of claim 1.
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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)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Abstract
A process for spectrally sensitizing photographic silver halide which comprises: adsorbing a photographic spectral sensitizing dye onto finely divided silica particles; and adding the dyed silica particles to a liquid photographic silver halide emulsion.
Description
States atent Ogilvie [S4] PRUCESS FOR SPECTRALLY SENSITIZING PHOTOGRAPHIC SILVER HALIDE EMULSIONS 21 Appl. No.: 761,841
[52] US. Cl ..96l120, 96/50 [51] Int. Cl. ..G03C 1/08, G03c 5/26 [58] Field of Search ..96/102, 50, 85, 86, 87, 106
[56] References Cited UNITED STATES PATENTS 3,469,987 Owens et a1. ..96/102 Mar. 14, 1972 OTHER PUBLICATIONS Allingham et al., Adsorption of Dyes and Related Compounds by Silica, Journal of Applied Chemistry," Vol. 8, February, 1958,1 108-116 Primary ExaminerDavid Klein Assistant Examiner-Edward C Kimlin Att0meyW. H. J. Kline, J. R. Frederick and O. H. Webster [5 7] ABSTRACT A process for spectrally sensitizing photographic silver halide which comprises: adsorbing a photographic spectral sensitizing dye onto finely divided silica particles; and adding the dyed silica particles to a liquid photographic silver halide emulsion.
14 Claims, No Drawings PROCESS FOR SPECTRALLY SENSITIZING PHOTOGRAPHIC SILVER HALIDE EMULSIONS This invention relates to novel photographic processes, and more particularly to novel processes for spectrally sensitizing photographic silver halide emulsions. It also relates to novel photographic emulsions and elements prepared by the process of this invention.
The conventional method of sensitizing silver halide emulsions consists of dissolving the sensitizing dye in an appropriate organic solvent such as methyl alcohol, ethyl alcohol, acetone, etc., and adding the resulting solution to the liquid emulsion. While this general method has provided a commercially feasible means for incorporating sensitizing dyes into silver halide emulsions, it introduces undesirable amounts of organic solvent into the emulsion, which can result in coating defects or wandering of the dye in various layers of a photographic element.
It is therefore, an object of this invention to provide a new and improved method for incorporating sensitizing dyes into photographic silver halide emulsions.
Another object of this invention is to provide an efficient, readily controllable means for incorporating sensitizing dyes into such emulsions.
Another object is to provide novel silver halide emulsions and elements.
Other objects of this invention will be apparent from this disclosure and the appended claims.
1 have made the important discovery that photographic spectral sensitizing dyes can be reversibly adsorbed to finely divided silica (SiO particles. When the dyed silica particles are incorporated into a liquid photographic silver halide emulsion, the spectral sensitizing dye transfers to the silver halide crystals, and becomes effectively adsorbed thereto. This results in spectral sensitization of the silver halide grains in the emulsion. The silica remains in photographic layers produced with emulsions prepared in accordance with this invention. The residual silica in the layers inhibits dye wandering and provides tooth which facilitates retouching or writing thereon.
The method of this invention fully overcomes the mentioned shortcomings of the prior art procedures. The need of using organic solvents in the prior art processes to incorporate the dyes into the emulsions is completely eliminated in the method ofthis invention.
Suitable silicas for practicing this invention include silicon dioxide particles having an average diameter ranging from about 0.001 to microns. Useful materials of this kind are commercially available under various trade names, e.g., Cabo-Sil, a colloidal silica manufactured by Godfrey L. Cabot, lnc.; Celite, a diatomaceous silica manufactured by John- Manville Sales Corp.; Nalcosil, a colloidal silica manufactured by Nalco Chem. Co.; Hi-Sil, an ultra-fine silica manufactured by Pittsburgh Plate Glass Co.; Si-O-Lite, fine silica manufactured by Mallinkrodt Chem. Co.; powdered silica gels and the like. The concentration of the silica which is most advantageously employed will depend, of course upon the silver halide emulsion employed and upon the sensitizing dye employed. Ordinarily, however, from about 10 to 150 g., but preferably from about to 50 g., of the silica per gram-mole of silver halide is advantageously used.
Suitable spectral sensitizing dyes for practicing the invention include any of those known to sensitize silver halide emulsions. Typical useful dyes include any of the methine dyes, such as the cyanine dyes (including the carbocyanines, the dicarbocyanines and complex cyanines); merocyanine dyes (including complex merocyanine dyes) and, styryl dyes. Typical dyes which can be used in the practice of this invention include any of those disclosed in the following patents, the disclosure of which is incorporated herein by reference.
Zeh et al. U.S. Pat. No. 2,068,047 issued l/l9/37 Brooker U.S. Pat. No. 2,078,233 issued 4/27/37 Koslowsky U.S. Pat. No. 2,107,279 issued 2/8/38 Mees U.S. Pat. No. 2,158,883 issued 5/16/39 Brooker et al. U.S. Pat. No. 2,161,331 issued 6/6/39 Brooker U.S. Pat. No. 2,170,807 issued 8/29/39 Brooker U.S. Pat. No. 2,177,402 issued 10/24/39 Brooker U.S. Pat. No. 2,177,403 issued 10/24/39 Carroll et al. U.S. Pat. No. 2,177,635 issued 10/31/39 Carroll U.S. Pat. No. 2,206,076 issued 7/2/40 Brooker U.S. Pat. No. 2,21 1,762 issued 8/20/40 Brooker et al. U.S. Pat. No. 2,213,238 issued 9/3/40 Brooker U.S. Pat. No. 2,307,916 issued 1/12/43 Brooker et al. U.S. Pat. No. 2,313,922 issued 3/16/43 Schneider U.S. Pat. No. 2,374,505 issued 4/24/45 Falleson et al. U.S. Pat. No. 2,378,917 issued 6/26/45 Brooker U.S. Pat. No. 2,454,629 issued 11/23/48 Thompson U.S. Pat. No. 2,535,993 issued 12/26/50 Carroll et al. U.S. Pat. No. 2,950,196 issued 8/23/60 Brooker et al. U.S. Pat. No. 2,955,939 issued 10/11/60 Jones U.S. Pat. No. 2,961,318 issued l1/22/60 Brooker et al. U.S. Pat. No. 3,194,805 issued 7/13/65 Tabor et al. U.S. Pat. No. 3,335,010 issued 8/8/67 Brooker et al. U.S. Reissue No. 24,292 reissued 3/19/57 I.G., British Pat. No. 434,235 accepted 8/28/35 The spectral sensitizing dye can be adsorbed to the silica in any convenient manner. Preferably, a spectral sensitizing dye is dissolved in an organic solvent for the dye, and the silica is mixed therewith. After the dye has become adsorbed to the silica, the organic solvent is advantageously removed in any convenient manner. Removal of the organic solvent is not essential to the practice of this invention; however, removal of the organic solvent is the preferred mode of carrying out the invention. Solvent removal can be accomplished in any convenient manner, e.g., by evaporation, filtration or centrifugmg.
The concentration of the sensitizing dye can with advantage range from about 0.001 to 0.200 g. per gram-mole ofsilver ha lide in the emulsion. Advantageously, the dye-containing silica particles are incorporated in the photographic silver halide emulsions at temperatures ranging about from 40 to 60 C.
The process of this invention is useful in spectrally sensitizing any of the photographic silver halides, including silver bromide, silver chloride, silver bromoiodide, silver chlorobromide, silver chloroiodide or silver chlorobromoiodide. The photographic grains can be dispersed in any suitable binder, including such hydrophilic binders as gelatin, albumin, agaragar, gum arabic, alginic acid, polyvinyl alcohol, polyvinyl pyrrolidone, cellulose ethers, partially hydrolyzed cellulose acetate, and the like. The binding agents for the emulsion layer of the photographic element can also contain dispersed polymerized vinyl compounds. Such compounds are disclosed, for example, in U. S. Pat. Nos. 3,142,568; 3,193,386; 3,062,674 and 3,220,844 and include the water insoluble polymers of alkyl acrylates and methacrylates, acrylic acid, sulfoalkyl acrylates or methacrylates and the like.
Emulsions sensitized as described herein can be coated on any suitable photographic support, such as glass, film base such as cellulose acetate, cellulose acetate butyrate, polyesters such as poly(ethylene terephthalate), paper, baryta coated paper, polyolefin coated paper, e.g., polyethylene or polypropylene coated paper, which may be electron bombarded to promote emulsion adhesion, to produce the novel photographic elements of the invention.
Emulsions sensitized in accordance with this invention can contain addenda such as chemical sensitizers, e.g., sulfur sensitizers (e.g., allyl thiocarbamate, thiourea, allyl-isothiocyanate, cystine, etcv) various gold compounds (e.g., potassium chloroaurate, auric trichloride, etc. (see Baldsiefen, U.S. Pat. No. 2,540,085, issued Feb. 6, 1951, Damschroder, U.S. Pat. No. 2,597,856, issued May 27, 1952 and Yutzy et al. U.S. Pat. No. 2,597,915 issued May 27, 1952), various palladium compounds such as palladium chloride (Baldsiefen, U.S. Pat. No. 2,540,086, issued Feb. 6, 1951), potassium chloropalladate (Stauffer et al., U.S. Pat. No. 2,598,079, issued May 27, 1952), etc., or mixtures of such sensitizers, antifoggants such as ammonium chloroplatinate Trivelli et al. U.S. Pat. No. 2,566,245, issued Aug. 28, 1951), ammonium chloroplatinite (Trivelli et al., U.S. Pat. No. 2,566,263, issued Aug. 28, 1951), benzotriazole, nitrobenzimidazole, 5-nitroimidazole,
benzidine, mercaptans, etc. (see MeesThe Theory of the Photographic Process, MacMillan Pub., 1942, page 460), or mixtures thereof. The silver halide emulsions of the invention can be hardened with any suitable hardener, including aldehyde hardeners such as formaldehyde, and mucochloric acid, aziridine hardeners, hardeners which are derivatives of dioxane, oxypolysaccharides such as oxy starch or oxy plant gums, and the like. The emulsion layers can also contain additional additives, particularly those known to be beneficial in photographic emulsions, including, for example, lubricating materials, stabilizers speed increasing materials, absorbing dyes, plasticizers, and the like. These photographic emulsions can also contain in some cases additional spectral sensitizing dyes. Furthermore, these emulsions can contain color-forming couplers or can be developed in solutions containing couplers or other color generating materials. Among the useful color formers are the monomeric and polymeric color formers, e.g., pyrazolone color formers, as well as phenolic, heterocyclic and open chain couplers having a reactive methylene group. The color-forming couplers can be incorporated into the photographic silver halide emulsion using any suitable technique, e.g., techniques of the type shown in Jelley et a1. U.S. Pat. No. 2,322,027, issued June 15, 1943, Fierke et a1. U.S. Pat. No. 2,801,171, issued July 30, 1957, Fisher U.S. Pat. Nos. 1,055,155 and 1,102,028, issued Mar. 4, 1913 and June 30, 1914, respectively, and Wilmanns U.S. Pat. No. 2,186,849, issued Jan. 9, 1949. They can also be developed using incorporated developers such as polyhydroxybenzenes, aminophenols, 3-pyrazolidones, and the like.
The following examples are included for a further understanding of this invention. Dyes used in the examples are identified in Table 1.
TABLE 1 Dye No. Dye Compound 1 l. 1 '-Diethyl-2,2'-cyunine chloride 11 Anhydro-5.5 '.6.6'-tetrachloro-l l-diethyl-3,3'-di( 3- sulfohutyl)benzirnidazolocarbocynnine hydroxide 111 3-( Il-Dimethylaminopropyl) $-l( 3-methyl-2- thiazolidinylidene )ethylidene ]-2-thi0-2.4- oxazolidinedione EXAMPLES l to 5 4 to 8 g. of each dye is dissolved in ml. of an appropriate solvent such as methyl alcohol. and each solution is then added to 1.0 g. of finely divided silica (Cab-O-sil, a trade name for colloidal silica manufactured by Godfrey L Cabot, lnc.). Each mixture is centrifuged to separate the dyes silica from the solvent. The samples of dyed silica are in each case dried and powdered. The ratio of dye to silica will vary depending on the starting dye concentration, on the absorbing time, etc. These conditions can be adjusted in each case to produce a dye concentration giving the optimum sensitizing results. The dyed silica in each instance is then added directly to a stirred aqueous gelatin silver bromoiodide emulsion at 40 C. containing 0.77 mole percent iodide of the type described by Trivelli and Smith, Phot. Journal, 79, 330 (1939). The same batch of emulsion is used in each sample. The melts are held in each case at 52 C., cooled to 40 C., hand coated onto a cellulose acetate film support at a coverage of 432 mg. silver per square foot, chill set and dried. A sample of each coating is-exposed to a wedge spectrograph, processed for 3 minutes in Kodak Developer D-l9 which has the following composition:
N-rnethyl-p-aminophenol sulfate 2.0 g. Hydroquinone 8.0 g. Sodium sulfite (desiccated) 90.0 g. Sodium carbonate lmonohydrate) 52.5 5. Potassium bromide 5.0 g.
Water to make 1.0 l.
and then fixed in a conventional sodium thiosulfate fixing bath, washed and dried. Densitometric measurements are then made of the developed images of each coating. The results are listed in the following Table 2 for sensitizing ranges and maximum sensitivities together with the respective concentrations of dye and silica corresponding to each of the examples.
Coating contained 1.66 g. 01 Loucophor Blmole of silver is stilbene type of brightening agent; colour index, 2nd edition, vol. 2, p. 2914).
Referring to the above table, it will be seen that in each of Examples 1 to 5 containing the indicated Dye Nos. 1, 11 and 111 the sensitivity is extended to the region of 560 to 615 nm. with maximum sensitivity occuring in the region of 5 l 5 to 580 nm., whereas the control example containing approximately the same amount of silica but containing no sensitizing dye shows sensitivity up to about 515 nm. with a maximum sensitivity at 440 nm. Accordingly, these results clearly indicate that the novel process of this invention provides a new, effective and very convenient means for incorporating sensitizing dyes in photographic silver halide emulsions. These results further show that the resulting emulsions and elements faithfully extend the sensitivity in accordance with the sensitizing characteristics of each of the individual dyes.
It will be apparent from the foregoing disclosure that practically any spectral sensitizing cyanine dye can be substituted in the above examples to given generally similar good quality, spectrally sensitized silver halide emulsions and elements.
Although the invention has been described in considerable detail with particular reference to certain preferred embodiments thereof, it will be understood that variations and modifications can be effected within the spirit and scope of the invention as described hereinabove, and as defined in the appended claims.
1 claim:
1. A process for spectrally sensitizing photographic silver halide which comprises: adsorbing a photographic spectral sensitizing dye onto finely divided silica particles; and, adding the dyed silica particles to a liquid photographic silver halide emulsion to transfer dye from the silica particles to the silver halide grains in said emulsion.
2. The process in accordance with claim 1 wherein said silica particles have an average diameter of from about 0.001 to 10 microns.
3. The process in accordance with claim 1 wherein said dye and said silica particles are present in proportions of about from 0.001 to 0.200 gram of said dye and about from 10 to grams of said silica per gram-mole of silver halide in said emulsion.
4. the process in accordance with claim 3 wherein the photographic silver halide emulsion is an aqueous gelatin silver halide emulsion.
5. The process in accordance with claim 1 wherein said spectral sensitizing dye is selected from the group consisting of a cyanine dye and a merocyanine dye.
6. A process for spectrally sensitizing photographic silver halide which comprises: dissolving a photographic spectral sensitizing dye in an organic solvent; mixing finely divided silica particles with a solution of dye in organic solvent to adsorb the dye onto the silica particles; removing the organic solvent; and, adding the dyed silica particles to a liquid photographic silver halide emulsion to transfer dye from the silica particles to the silver halide grains in said emulsion.
7. The process in accordance with claim 6, wherein said silica particles have an average diameter of from about 0.001 to microns.
8. The process in accordance with claim 6 wherein said dye and said silica particles are present in the proportions of about from 0.001 to 0.200 gram of said dye and about from 10 to 150 grams of said silica per gram-mole of silver halide in said emulsion.
9. The process in accordance with claim 8 wherein the photographic silver halide emulsion in an aqueous gelatin silver halide emulsion.
10. The process in accordance with claim 3 wherein said silica particles comprise colloidal silica and said dye is a 1,1- diethyl-2,2-cyanine salt.
1 1. The process in accordance with claim 3 wherein said silica particles comprise colloidal silica and said dye is anhydro- 5,5,6,6 1,! '-diethyl-3,3'-di(3-sulfobutyl)- benzimidazolocarbocyanine hydroxide.
12. The process in accordance with claim 3 wherein said silica particles comprise colloidal silica and said dye is 3-( 3- dimethylaminopropyl )-5- -2-thio-2,4-oxazolidinedione.
13. A photographic silver halide emulsion prepared by the process of claim 1.
14. A photographic element comprising a support having thereon a layer containing a photographic silver halide emulsion prepared by the process of claim 1.
Claims (13)
- 2. The process in accordance with claim 1 wherein said silica particles have an average diameter of from about 0.001 to 10 microns.
- 3. The process in accordance with claim 1 wherein said dye and said silica particles are present in proportions of about from 0.001 to 0.200 gram of said dye and about from 10 to 150 grams of said silica per gram-mole of silver halide in said emulsion.
- 4. the process in accordance with claim 3 wherein the photographic silver halide emulsion is an aqueous gelatin silver halide emulsion.
- 5. The process in accordance with claim 1 wherein said spectral sensitizing dye is selected from the group consisting of a cyanine dye and a merocyanine dye.
- 6. A process for spectrally sensitizing photographic silver halide which comprises: dissolving a photographic spectral sensitizing dye in an organic solvent; mixing finely divided silica particles with a solution of dye in organic solvent to adsorb the dye onto the silica particles; removing the organic solvent; and, adding the dyed silica particles to a liquid photographic silver halide emulsion to transfer dye from the silica particles to the silver halide grains in said emulsion.
- 7. The process in accordance with claim 6, wherein said silica particles have an average diameter of from about 0.001 to 10 microns.
- 8. The process in accordance with claim 6 wherein said dye and said silica particles are present in the proportions of about from 0.001 to 0.200 gram of said dye and about from 10 to 150 grams of said silica per gram-mole of silver halide in said emulsion.
- 9. The process in accordance with claim 8 wherein the photographic silver halide emulsion is an aqueous gelatin silver halide emulsion.
- 10. The process in accordance with claim 3 wherein said silica particles comprise colloidal silica and said dye is a 1,1''-diethyl-2,2''-cyanine salt.
- 11. The process in accordance with claim 3 wherein said silica particles comprise colloidal silica and said dye is anhydro-5,5'', 6,6''-tetrachloro-1,1''-diethyl-3,3''-di(3-sulfobutyl) -benzimidazolocarbocyanine hydroxide.
- 12. The process in accordance with claim 3 wherein said silica particles comprise colloidal silica and said dye is 3-(3-dimethylaminopropyl)-5- -2-thio-2,4-oxazolidinedione.
- 13. A photographic silver halide emulsion prepared by the process of claim 1.
- 14. A photographic element comprising a support having thereon a layer containing a photographic silver halide emulsion prepared by the process of claim 1.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US76184168A | 1968-09-23 | 1968-09-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3649286A true US3649286A (en) | 1972-03-14 |
Family
ID=25063391
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US761841A Expired - Lifetime US3649286A (en) | 1968-09-23 | 1968-09-23 | Process for spectrally sensitizing photographic silver halide emulsions |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3649286A (en) |
| BE (1) | BE739220A (en) |
| DE (1) | DE1947935A1 (en) |
| FR (1) | FR2018644A1 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4134769A (en) * | 1976-08-10 | 1979-01-16 | Mitsubishi Paper Mills, Ltd. | Offset printing plate |
| US4771866A (en) * | 1986-04-03 | 1988-09-20 | Enertrols, Inc. | Shock absorber with proximity switch |
| US5077183A (en) * | 1987-12-24 | 1991-12-31 | Agfa Gevaert Aktiengesellschaft | Color photographic recording material and a process for the preparation of a photographic silver halide emulsion |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3469987A (en) * | 1965-06-21 | 1969-09-30 | Eastman Kodak Co | Method of spectrally sensitizing photographic silver halide emulsions |
-
1968
- 1968-09-23 US US761841A patent/US3649286A/en not_active Expired - Lifetime
-
1969
- 1969-09-22 DE DE19691947935 patent/DE1947935A1/en active Pending
- 1969-09-22 FR FR6932099A patent/FR2018644A1/fr not_active Withdrawn
- 1969-09-22 BE BE739220D patent/BE739220A/xx unknown
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3469987A (en) * | 1965-06-21 | 1969-09-30 | Eastman Kodak Co | Method of spectrally sensitizing photographic silver halide emulsions |
Non-Patent Citations (1)
| Title |
|---|
| Allingham et al., Adsorption of Dyes and Related Compounds by Silica, Journal of Applied Chemistry, Vol. 8, February, 1958, pp. 108 116 * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4134769A (en) * | 1976-08-10 | 1979-01-16 | Mitsubishi Paper Mills, Ltd. | Offset printing plate |
| US4771866A (en) * | 1986-04-03 | 1988-09-20 | Enertrols, Inc. | Shock absorber with proximity switch |
| US5077183A (en) * | 1987-12-24 | 1991-12-31 | Agfa Gevaert Aktiengesellschaft | Color photographic recording material and a process for the preparation of a photographic silver halide emulsion |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2018644A1 (en) | 1970-06-26 |
| BE739220A (en) | 1970-03-02 |
| DE1947935A1 (en) | 1970-04-23 |
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