US3173789A - Method and composition for inhibiting silver sludge in thiosulfate monobaths - Google Patents
Method and composition for inhibiting silver sludge in thiosulfate monobaths Download PDFInfo
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- US3173789A US3173789A US169668A US16966862A US3173789A US 3173789 A US3173789 A US 3173789A US 169668 A US169668 A US 169668A US 16966862 A US16966862 A US 16966862A US 3173789 A US3173789 A US 3173789A
- Authority
- US
- United States
- Prior art keywords
- silver
- silver halide
- monobath
- photographic
- thiosulfate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229910052709 silver Inorganic materials 0.000 title claims description 90
- 239000004332 silver Substances 0.000 title claims description 90
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 title claims description 35
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 title claims 2
- 239000000203 mixture Substances 0.000 title description 45
- 239000010802 sludge Substances 0.000 title description 16
- 238000000034 method Methods 0.000 title description 14
- 230000002401 inhibitory effect Effects 0.000 title description 2
- -1 SILVER HALIDE Chemical class 0.000 claims description 77
- 239000003795 chemical substances by application Substances 0.000 claims description 33
- 239000000839 emulsion Substances 0.000 claims description 22
- 239000000243 solution Substances 0.000 claims description 19
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims description 12
- 230000001603 reducing effect Effects 0.000 claims description 12
- 239000012670 alkaline solution Substances 0.000 claims description 10
- 238000011161 development Methods 0.000 claims description 8
- 229940100890 silver compound Drugs 0.000 claims description 4
- 150000003379 silver compounds Chemical class 0.000 claims description 4
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 20
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical compound O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 13
- 230000015572 biosynthetic process Effects 0.000 description 9
- 125000000623 heterocyclic group Chemical group 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 6
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 5
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- 229910021607 Silver chloride Inorganic materials 0.000 description 4
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 4
- 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 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- GGZHVNZHFYCSEV-UHFFFAOYSA-N 1-Phenyl-5-mercaptotetrazole Chemical compound SC1=NN=NN1C1=CC=CC=C1 GGZHVNZHFYCSEV-UHFFFAOYSA-N 0.000 description 2
- JAAIPIWKKXCNOC-UHFFFAOYSA-N 1h-tetrazol-1-ium-5-thiolate Chemical class SC1=NN=NN1 JAAIPIWKKXCNOC-UHFFFAOYSA-N 0.000 description 2
- VEUMBMHMMCOFAG-UHFFFAOYSA-N 2,3-dihydrooxadiazole Chemical compound N1NC=CO1 VEUMBMHMMCOFAG-UHFFFAOYSA-N 0.000 description 2
- RUBRCWOFANAOTP-UHFFFAOYSA-N 3h-1,3,4-oxadiazole-2-thione Chemical class S=C1NN=CO1 RUBRCWOFANAOTP-UHFFFAOYSA-N 0.000 description 2
- JLAMDELLBBZOOX-UHFFFAOYSA-N 3h-1,3,4-thiadiazole-2-thione Chemical class SC1=NN=CS1 JLAMDELLBBZOOX-UHFFFAOYSA-N 0.000 description 2
- FOHWXVBZGSVUGO-UHFFFAOYSA-N 5-phenyl-3h-1,3,4-oxadiazole-2-thione Chemical compound O1C(S)=NN=C1C1=CC=CC=C1 FOHWXVBZGSVUGO-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- ZSILVJLXKHGNPL-UHFFFAOYSA-L S(=S)(=O)([O-])[O-].[Ag+2] Chemical compound S(=S)(=O)([O-])[O-].[Ag+2] ZSILVJLXKHGNPL-UHFFFAOYSA-L 0.000 description 2
- 150000002391 heterocyclic compounds Chemical class 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 230000001376 precipitating effect Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 2
- 235000019345 sodium thiosulphate Nutrition 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 229960004418 trolamine Drugs 0.000 description 2
- FKASFBLJDCHBNZ-UHFFFAOYSA-N 1,3,4-oxadiazole Chemical compound C1=NN=CO1 FKASFBLJDCHBNZ-UHFFFAOYSA-N 0.000 description 1
- CBDMBBKKGFKNCA-UHFFFAOYSA-N 1,5-diphenylpyrazolidin-3-one Chemical compound N1C(=O)CC(C=2C=CC=CC=2)N1C1=CC=CC=C1 CBDMBBKKGFKNCA-UHFFFAOYSA-N 0.000 description 1
- HLESEOXHRZRIAG-UHFFFAOYSA-N 1-(1,3-benzothiazol-2-yl)pyrazolidin-3-one Chemical compound N1C(=O)CCN1C1=NC2=CC=CC=C2S1 HLESEOXHRZRIAG-UHFFFAOYSA-N 0.000 description 1
- MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-UHFFFAOYSA-N 0.000 description 1
- XWKAZXKJYHZGAI-UHFFFAOYSA-N 2-acetyl-4,4-dimethyl-1-phenylpyrazolidin-3-one Chemical compound C1C(C)(C)C(=O)N(C(=O)C)N1C1=CC=CC=C1 XWKAZXKJYHZGAI-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
- SJSJAWHHGDPBOC-UHFFFAOYSA-N 4,4-dimethyl-1-phenylpyrazolidin-3-one Chemical compound N1C(=O)C(C)(C)CN1C1=CC=CC=C1 SJSJAWHHGDPBOC-UHFFFAOYSA-N 0.000 description 1
- ZZEYCGJAYIHIAZ-UHFFFAOYSA-N 4-methyl-1-phenylpyrazolidin-3-one Chemical compound N1C(=O)C(C)CN1C1=CC=CC=C1 ZZEYCGJAYIHIAZ-UHFFFAOYSA-N 0.000 description 1
- HNFIJWNVPWXSOL-UHFFFAOYSA-N 5-(2-methylphenyl)-3h-1,3,4-oxadiazole-2-thione Chemical compound CC1=CC=CC=C1C1=NNC(=S)O1 HNFIJWNVPWXSOL-UHFFFAOYSA-N 0.000 description 1
- WRBROPFHVKCQKV-UHFFFAOYSA-N 5-(3-nitrophenyl)-3h-1,3,4-oxadiazole-2-thione Chemical compound [O-][N+](=O)C1=CC=CC(C=2OC(=S)NN=2)=C1 WRBROPFHVKCQKV-UHFFFAOYSA-N 0.000 description 1
- ABSVCMBOXHMZPV-UHFFFAOYSA-N 5-(4-nitrophenyl)-3h-1,3,4-oxadiazole-2-thione Chemical compound C1=CC([N+](=O)[O-])=CC=C1C1=NN=C(S)O1 ABSVCMBOXHMZPV-UHFFFAOYSA-N 0.000 description 1
- AIZIJSLXZMNAGM-UHFFFAOYSA-N 5-cyclohexyl-3h-1,3,4-thiadiazole-2-thione Chemical compound S1C(=S)NN=C1C1CCCCC1 AIZIJSLXZMNAGM-UHFFFAOYSA-N 0.000 description 1
- FIARATPVIIDWJT-UHFFFAOYSA-N 5-methyl-1-phenylpyrazolidin-3-one Chemical compound CC1CC(=O)NN1C1=CC=CC=C1 FIARATPVIIDWJT-UHFFFAOYSA-N 0.000 description 1
- GQUZTSGWULGOLE-UHFFFAOYSA-N C(C)(=O)O[C-]1NN(CC1=O)C1=CC=CC=C1 Chemical compound C(C)(=O)O[C-]1NN(CC1=O)C1=CC=CC=C1 GQUZTSGWULGOLE-UHFFFAOYSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
- 229910052946 acanthite Inorganic materials 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- AJPXTSMULZANCB-UHFFFAOYSA-N chlorohydroquinone Chemical compound OC1=CC=C(O)C(Cl)=C1 AJPXTSMULZANCB-UHFFFAOYSA-N 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000004689 octahydrates Chemical class 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- XUARKZBEFFVFRG-UHFFFAOYSA-N silver sulfide Chemical compound [S-2].[Ag+].[Ag+] XUARKZBEFFVFRG-UHFFFAOYSA-N 0.000 description 1
- 229940056910 silver sulfide Drugs 0.000 description 1
- NVIFVTYDZMXWGX-UHFFFAOYSA-N sodium metaborate Chemical compound [Na+].[O-]B=O NVIFVTYDZMXWGX-UHFFFAOYSA-N 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/38—Fixing; Developing-fixing; Hardening-fixing
- G03C5/383—Developing-fixing, i.e. mono-baths
Definitions
- Monobaths containing a water-soluble thiosulfato, such as sodium thiosulfate, as the fixing agent has been known for a number of years.
- Monobath compositions offer in viting possibilities for processing an exposed photographic silver halide emulsion to produce a silver image because development and fixation or stabilization (of unexposed silver halide) can be accomplished in one simple operation.
- an object of our invention to provide a method of controllin the formation and deposition of silver sludge in monobath compositions for processing silver halide photographic materials. Another object is to provide a method of continuous processing of large amounts of photographic silver halide materials over extended periods of time without the disadvantages accompanying the formation of silver sludge. Still another object is to provide novel compositions of matter useful in monobath processing. Other objects will become apparent from a consideration of the following description and examples.
- photographic silver halide materials which have been exposed in the normal manner are subjected to monobath processing employing alkaline aqueous developing solutions containing one or more photographic developers capable of reducing exposed silver halide to metallic silver, a Water-soluble thiosulfate, in sufficient quantity to stabilize or remove substantially all unexposed silver halide, and a water-soluble heterocyclic mercapto compound.
- alkaline aqueous developing solutions containing one or more photographic developers capable of reducing exposed silver halide to metallic silver, a Water-soluble thiosulfate, in sufficient quantity to stabilize or remove substantially all unexposed silver halide, and a water-soluble heterocyclic mercapto compound.
- a number of heterocyclic compounds have been previously employed in photographic emulsions or developing compositions for the purpose of controlling image tone.
- the mercapto compounds useful in our invention are unique in controlling or preventing the formation of silver sludge during monobath processing.
- Heterocyclic mercapto compounds closely related to those used in our invention frequently have little or no useful activity in preventing the formation of silver sludge during monobath processing.
- Z-mercapto-5-o-hydroxyphenyll,3,4-thiadiazole is especially useful in our invention in preventing the formation of silver sludge, while the isomeric para hydroxy compound has little or no observable effect in preventing or controlling the formation of silver sludge.
- heterocyclic mercapto compounds of our invention comprise 1-phenyl-5-mercaptotetrazole, 2-mercapto-S-o-hydroxyphenyl-1,3,4 thiadiazole, 2 mercapto 5 o-tolyl-l,3,4-oxadiazole, 2-mercapto-5-phenyl- 1,3,4-oxadiazole, 2-mercapto-5-p-nitrophenyl-1,3,4-oxadiazole, 2-mercapto-5-cyclohexyl-1,3,4-thiadiazole, 2 mercapto5-m-nitrophenyl-1,3,4-oxadiazole, etc.
- Another useful heterocyclic compound for processing certain photographic silver halide emulsions is Z-benzoxazolethiol.
- This benzoxazole compound is useful in processing high speed negative photographic silver bromiodide emulsions.
- the monobath compositions of our invention are generally quite useful in processing a variety of photographic silver halide materials Where the silver halide can be, for example, silver chloride, silver bromide, silver chloro bromide, silver bromiodide, silver chlorobrorniodide, etc.
- the monobath compositions of our invention can comprise any of the conventional water-soluble thiosulfate fixing agents, such as the alkali metal, e.g., sodium, potassium, etc, thiosulfates, ammonium thiosulfate, etc.
- the concentration of the thiosulfate compound can be varied, but it is important to have the concentration sufficiently high to fix or stabilize substantially all of the unexposed silver halide.
- the thiosulfate concentration should be at least about grams per liter.
- the maximum concentration of thiosulfate is primarily a function of the concentration of the silver halide in the emulsion being processed.
- concentrations as high as grams of thiosulfate per liter of monobath composition can be employed and good quality prints can be produced in 5 seconds or less using such compositions.
- concentration of silver halide in the emulsion is increased, then it is possible that amounts of thiosulfate in excess of 160 grams per liter can be employed.
- the concentration of heterocyclic mercaptan used in our invention can be varied, but We have found that especially useful results can be obtained Where the concentration varies from about 0.001 gram per liter to about 1.0 gram per liter, with especially useful results being obtained Within the range of about 0.1 to about 0.5 gram per liter.
- the heterocyclic mercaptan need not be employed in the form of the free mercaptan, but can be used in the form of a Water-soluble salt, such as sodium, potassium, etc.
- the pH of the monobath compositions of our invention can be varied, but especially useful results have been obtained at pHs of at least about 10' to pHs as high as about 12 or 12.5.
- any of the ordinarily employed silver halide developing agents for rapidly producing a silver image can be employed in our invention. Especially useful results have been obtained using the well known 3-pyrazolidone developing agents. A number of such developing agents are described in the copending application, Serial No. 134,014, filed August '5, 1961, now abandoned, of P. H. Steward, G. E. Fallesen and J. W. Reeves, Jr.
- Typical of pyrazolidone developing agents useful in the monobath compositions of our invention include l-phenyl 3 :pyrazolidone, 1 phenyl 4,4 dimethyl 3- pyrazolidone, 1-phenyl-5-methyl-3-pyrazolidone, l-phenyl 4 methyl 3 pyrazolidone, 1,5 diphenyl 3- pyrazolidone, 1-p to1yl-3-pyrazolidone, 1-phenyl-2-acetyl- 4,4-dimethyl-3-pyrazolidone (acetyl group hydrolyses off to yield active developing agent), l-p-hydroxyphenyl- 4,4 dimethyl 3 pyrazolidone, 1 (2 benzothiazolyl) 3 pyrazolidone, 3 acetoxy l phenyl 3- pyrazolidone (acetoxy group hydrolyses off to yield active developer), etc.
- 3-pyrazolidone developing agents are particularly useful and they can be incorporated partly or Wholly within the photographic element undergoing development. However, for rapid monobath processing, it is desirable to generally have sufficient pyrazolidone developing agent in the aqueous developing solution to effect rapid processing.
- black-and-white photographic developing agents which can be employed alone or in combination with the 3-pyrazolidone include hydroquinone, N-methyl-p-arninophenyl sulfate, chlorohydroquinone, etc.
- the concentration of the developing agent in the monobath composition can be varied, depending upon the particular photographic material undergoing development.
- the 3-pyrazolidone developing agents are particularly useful, since they can be incorporated directly into the photographic material either in a layer contiguous to the emulsion layer or in the emulsion layer itself (particularly where a development precursor is used, such as 3-acetoxy-l-phenyl-3-pyrazolidone).
- Example 1 The following photographic monobath composition was prepared:
- Example 2 Photographic papers comprising an ordinary photographic silver chloride emulsion were processed in a monobath composition similar to that described in Example 1 above, except that it contained 0.2 gram per liter of 2-mercapto-S-o-hydroxyphenyl-1,3,4-thiadiazole instead of the tetrazole compound. After 20 prints had been processed through this monobath composition and the composition allowedto stand for 24 hours, the monobath composition remained sludge-free.
- Example 3 The 1-phenyl-S-mercaptotetrazole of Example 1 was replaced with 0.2 gram per liter of Z-mercapto-S-o-tolyh 1,3,4-oxadiazole. After processing 20 photographic paper sheets comprising an ordinary photographic silver chloride emulsion in this monobath and allowing it to stand for 24 hours, no sludge could be detected.
- Example '4 The phenyl mercaptotetrazole of Example 1 was replaced with 0.2 gram per liter of Z-mercapto-S-phenyl- 1,3,4-oxadiazole. Again, the monobath composition remained sludge-free at least 24 hours after processing 20 photographic prints.
- One commercially available monobath preparation currently available contains sodium .thiosulfate, and it is recommended to use room temperature processing for 5 to 8 minutes. It is stated that a print capacity of 8000 square inches of paper per gallon of monobath is possible using this composition. 'In commercial processing, it has frequently been found that useful capacity of separate developers and fixers seldom exceeds 10,000 square inches per gallon of either developer or fixer. Contrasted with the foregoing, we have found that the useful tray capacity of the monobath compositions of our invention is extended to 70,000 square inches of paper per gallon for a period exceeding two weeks. This increased processing capacity is realized .without deleterious changes in photographic quality during this period.
- hydroxyalkylamine compounds useful in our invention include ethanolamine, 2,2'-irninodiethanol, 2,2,2"-nitrilotriethanol -(triethanolamine), N-monomethylethanolamine, N-monoethylethanolamine, N,N-dimethylethanolamine, N,N-diethylethanolamine, etc.
- Particularly useful hydroxyalkylamines include those represented by the following general formula:
- R and R each represents a hydrogen atom, a lower alkyl radical (e.g., methyl, ethyl, propyl, etc), or a hydroxyalkyl radical (e.g., fi-hydroxyethyl, [3-hydroxypropyl, etc.).
- a lower alkyl radical e.g., methyl, ethyl, propyl, etc
- a hydroxyalkyl radical e.g., fi-hydroxyethyl, [3-hydroxypropyl, etc.
- a particularly useful monobath composition was prepared according to the method described in Example 1 above by including about 9 grams of ethanolamine in the composition.
- the combination of the mercaptotetrazole compound and the ethanolamine compound gave particularly useful results, insofar as freedom from sludge and development speed were concerned. Excellent photographic quality was obtained using such combinations.
- the amount of hydroxyalkyl compound used can be varied. We have found that from about 5 to 20 grams per liter give quite useful effects.
- a monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thiosulfate, a Water-soluble hydroxyalkylamine, and from about 0.001 to about 1.0 gram per liter of solution of a heterocyclic mercaptan capable of adsorbing silver compounds formed by photographic development to solubilize such silver compounds, said heterocyclic mercaptan being selected from the class consisting of mercaptotetrazoles, mercapto-1,3,4-oxadiazoles and mercapto-1,3,4-thiadiazoles.
- a monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thiosulfate, and from about 0.001 to about 10 gram per liter of a water-soluble heterocyclic mercaptan which renders silver containing precipitating nuclei soluble upon adsorption of said mercaptan thereto, said heterocyclic mercaptan being selected from the class consisting of mercaptotetrazoles, mercapto-1,3,4-oxadiazoles and mercapto- 1,3,4-thiadiazoles.
- a monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thiosulfate, and from about 0.001 to about 1.0 gram per liter of 1- phenyl-S-mercaptotetrazole.
- a monobath composition for simultaneously developing andfixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thiosulfate, and from about 0.001 to about 1.0 gram per liter of 2- mercapto-S-o-hydroxyphenyl-1,3,4-thiadiazole.
- a monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least grams per liter of solution of a water-soluble thiosulfate, and from about 0.001 to about 1.0 gram per liter of 2- mercapto-S-o-tolyl-1,3,4-oxadiazole.
- a monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thiosulfate, and from about 0.001 to about 1.0 gram per liter of 2- mercapto-5-phenyl-1,3,4-oxadiazole.
- a monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a Water-soluble thiosulfate, and from about 0.001 to about 1.0 gram per liter of Z-mercapto-S-p-nitrophenyl-1,3,4-oxadiazole.
- a monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thiosulfate, and from about 0.001 to about 1.0 gram per liter of Z-mercapto-S-cyclohexyl-1,3,4-thiadiazole.
- a monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thicsulfate, and from about 0.001 to about 1.0 gram per liter of 2-mercapto-S-m-nitrophenyl-1,3,4-oxadiazole.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Description
United States Patent 3,173,789 METHOD AND COMPGSITEGN FUR INHEBI'HNG SILVER SLUDGE IN THIGSULFATE MONOBATHS James R. King and demos R. Moran, Rochester, N-Y assignors to Eastman Kodak QOmpany, Rochester, N.Y., a corporation of New .ierscy No Drawing. Filed Jan. 29, 1962, Ser. No. teases 18 Claims. (Cl. 66ll) This invention relates to photography and, more particularly, to a method and composition for preventing and/or inhibiting the formation of silver sludge during photographic processing employing a monobath containing a thiosulfate fixing agent.
Monobaths containing a water-soluble thiosulfato, such as sodium thiosulfate, as the fixing agent has been known for a number of years. Monobath compositions offer in viting possibilities for processing an exposed photographic silver halide emulsion to produce a silver image because development and fixation or stabilization (of unexposed silver halide) can be accomplished in one simple operation.
However, one of the major disadvantages accompanying the use of such monobath compositions is the formation and deposition of silver sludge when the monobath composition is employed to process photographic silver halide materials in a continuous manner. See H. A. Miller and J. I. Crabtree-Amer. Phot, vol. 42. (1948), page 76 and W. M. Drumm-Phot. Sci. and Eng, vol. 1 (1958), page 147. If the monobath is warmed slightly to increase the rate of processing, this has the further disadvantage of accelerating the deposition of the undesir able silver sludge. More often than not, these silver deposits cling to equipment as well as processed materials, and are difficult to remove.
Attempts have been previously made to control silver sludging in monobaths by a variety of techniques, one method being to employ coagulants to cause the silver sludge to settle to the bottom of the processing solution. Another technique is to use active nuclei, or silver precipitating agents, such as Carey-Lea silver. While these methods do have some eifect upon the degree of sludging, they are not able to substantially eliminate the sludge, or to inhibit the formation of such sludge for a period of time sufiiciently long to make continuous processing possible.
We have now found that the problem of silver sludging in thiosulfate monobaths can be substantially eliminated or controlled by using certain mercapto compounds in the monobath composition.
It is, therefore, an object of our invention to provide a method of controllin the formation and deposition of silver sludge in monobath compositions for processing silver halide photographic materials. Another object is to provide a method of continuous processing of large amounts of photographic silver halide materials over extended periods of time without the disadvantages accompanying the formation of silver sludge. Still another object is to provide novel compositions of matter useful in monobath processing. Other objects will become apparent from a consideration of the following description and examples.
According to our invention, photographic silver halide materials which have been exposed in the normal manner are subjected to monobath processing employing alkaline aqueous developing solutions containing one or more photographic developers capable of reducing exposed silver halide to metallic silver, a Water-soluble thiosulfate, in sufficient quantity to stabilize or remove substantially all unexposed silver halide, and a water-soluble heterocyclic mercapto compound. A number of heterocyclic compounds have been previously employed in photographic emulsions or developing compositions for the purpose of controlling image tone. However, we have found that the mercapto compounds useful in our invention are unique in controlling or preventing the formation of silver sludge during monobath processing. Heterocyclic mercapto compounds closely related to those used in our invention frequently have little or no useful activity in preventing the formation of silver sludge during monobath processing. For example, Z-mercapto-5-o-hydroxyphenyll,3,4-thiadiazole is especially useful in our invention in preventing the formation of silver sludge, while the isomeric para hydroxy compound has little or no observable effect in preventing or controlling the formation of silver sludge.
Particularly useful heterocyclic mercapto compounds of our invention comprise 1-phenyl-5-mercaptotetrazole, 2-mercapto-S-o-hydroxyphenyl-1,3,4 thiadiazole, 2 mercapto 5 o-tolyl-l,3,4-oxadiazole, 2-mercapto-5-phenyl- 1,3,4-oxadiazole, 2-mercapto-5-p-nitrophenyl-1,3,4-oxadiazole, 2-mercapto-5-cyclohexyl-1,3,4-thiadiazole, 2 mercapto5-m-nitrophenyl-1,3,4-oxadiazole, etc. Another useful heterocyclic compound for processing certain photographic silver halide emulsions is Z-benzoxazolethiol. This benzoxazole compound is useful in processing high speed negative photographic silver bromiodide emulsions. The monobath compositions of our invention are generally quite useful in processing a variety of photographic silver halide materials Where the silver halide can be, for example, silver chloride, silver bromide, silver chloro bromide, silver bromiodide, silver chlorobrorniodide, etc.
The monobath compositions of our invention can comprise any of the conventional water-soluble thiosulfate fixing agents, such as the alkali metal, e.g., sodium, potassium, etc, thiosulfates, ammonium thiosulfate, etc. The concentration of the thiosulfate compound can be varied, but it is important to have the concentration sufficiently high to fix or stabilize substantially all of the unexposed silver halide. For the purposes of our invention, we have found that the thiosulfate concentration should be at least about grams per liter. The maximum concentration of thiosulfate is primarily a function of the concentration of the silver halide in the emulsion being processed. Frequently, concentrations as high as grams of thiosulfate per liter of monobath composition can be employed and good quality prints can be produced in 5 seconds or less using such compositions. Of course, if the concentration of silver halide in the emulsion is increased, then it is possible that amounts of thiosulfate in excess of 160 grams per liter can be employed.
The concentration of heterocyclic mercaptan used in our invention can be varied, but We have found that especially useful results can be obtained Where the concentration varies from about 0.001 gram per liter to about 1.0 gram per liter, with especially useful results being obtained Within the range of about 0.1 to about 0.5 gram per liter. The heterocyclic mercaptan need not be employed in the form of the free mercaptan, but can be used in the form of a Water-soluble salt, such as sodium, potassium, etc.
The pH of the monobath compositions of our invention can be varied, but especially useful results have been obtained at pHs of at least about 10' to pHs as high as about 12 or 12.5.
Any of the ordinarily employed silver halide developing agents for rapidly producing a silver image can be employed in our invention. Especially useful results have been obtained using the well known 3-pyrazolidone developing agents. A number of such developing agents are described in the copending application, Serial No. 134,014, filed August '5, 1961, now abandoned, of P. H. Steward, G. E. Fallesen and J. W. Reeves, Jr. Typical of pyrazolidone developing agents useful in the monobath compositions of our invention include l-phenyl 3 :pyrazolidone, 1 phenyl 4,4 dimethyl 3- pyrazolidone, 1-phenyl-5-methyl-3-pyrazolidone, l-phenyl 4 methyl 3 pyrazolidone, 1,5 diphenyl 3- pyrazolidone, 1-p to1yl-3-pyrazolidone, 1-phenyl-2-acetyl- 4,4-dimethyl-3-pyrazolidone (acetyl group hydrolyses off to yield active developing agent), l-p-hydroxyphenyl- 4,4 dimethyl 3 pyrazolidone, 1 (2 benzothiazolyl) 3 pyrazolidone, 3 acetoxy l phenyl 3- pyrazolidone (acetoxy group hydrolyses off to yield active developer), etc. These 3-pyrazolidone developing agents are particularly useful and they can be incorporated partly or Wholly within the photographic element undergoing development. However, for rapid monobath processing, it is desirable to generally have sufficient pyrazolidone developing agent in the aqueous developing solution to effect rapid processing. black-and-white photographic developing agents which can be employed alone or in combination with the 3-pyrazolidone include hydroquinone, N-methyl-p-arninophenyl sulfate, chlorohydroquinone, etc. The concentration of the developing agent in the monobath composition can be varied, depending upon the particular photographic material undergoing development. As indicated above, the 3-pyrazolidone developing agents are particularly useful, since they can be incorporated directly into the photographic material either in a layer contiguous to the emulsion layer or in the emulsion layer itself (particularly where a development precursor is used, such as 3-acetoxy-l-phenyl-3-pyrazolidone).
The following examples will serve to illustrate briefly the operation'of our invention.
Example 1 The following photographic monobath composition was prepared:
' Grams 4-methyl-1-phenyl-3-pyrazolidone 4.0 Hydroquinone 12.0 Sodium sulfite, desiccated 70.0 Sodium hydroxide 3.0 Sodium metaborate, octahydrate 40.0 Sodium thiosulfate, crystalline 100.0 Water to make 10.2 pH=10.2.
' One liter of the above monobath was used to process '20 sheets, 8 /2 x 1-1 inches, of exposed silver chloride document copying photographic paper for a period of 10 seconds at room temperature. upon standing for one hour, the used monobath solution produced'a heavy gray to. black precipitate which deposited upon the ves- Other of black particles could be seen. The prints had image density, fog and stability characteristics equal or superior to those processed in the monobath containing no mercaptotetrazole compound.
Example 2 Photographic papers comprising an ordinary photographic silver chloride emulsion were processed in a monobath composition similar to that described in Example 1 above, except that it contained 0.2 gram per liter of 2-mercapto-S-o-hydroxyphenyl-1,3,4-thiadiazole instead of the tetrazole compound. After 20 prints had been processed through this monobath composition and the composition allowedto stand for 24 hours, the monobath composition remained sludge-free.
Example 3 The 1-phenyl-S-mercaptotetrazole of Example 1 was replaced with 0.2 gram per liter of Z-mercapto-S-o-tolyh 1,3,4-oxadiazole. After processing 20 photographic paper sheets comprising an ordinary photographic silver chloride emulsion in this monobath and allowing it to stand for 24 hours, no sludge could be detected.
Example '4 The phenyl mercaptotetrazole of Example 1 was replaced with 0.2 gram per liter of Z-mercapto-S-phenyl- 1,3,4-oxadiazole. Again, the monobath composition remained sludge-free at least 24 hours after processing 20 photographic prints.
In a manner described in the above examples, other tetrazole, thiadiazole and oxadiazole compounds of this type described above can be employed to prevent silver sludging in monobath compositions comprising both developing agent and fixing or stabilizing agent. While the mechanism of our invention is not fully understood, it is believed that it is concerned with rendering silver and/or silver sulfide nuclei, produced on development and fixation, incapable of catalyzing the reduction of the silver thiosulfate complex 'by'strong adsorption of the heterocyclic mercaptan to the nuclei; If the adsorbed nuclei are soluble, no sludging occurs, but if these adsorbed nuclei are not sufficiently soluble in the monobath, a white or near white precipitate is immediately formed.
One commercially available monobath preparation currently available contains sodium .thiosulfate, and it is recommended to use room temperature processing for 5 to 8 minutes. It is stated that a print capacity of 8000 square inches of paper per gallon of monobath is possible using this composition. 'In commercial processing, it has frequently been found that useful capacity of separate developers and fixers seldom exceeds 10,000 square inches per gallon of either developer or fixer. Contrasted with the foregoing, we have found that the useful tray capacity of the monobath compositions of our invention is extended to 70,000 square inches of paper per gallon for a period exceeding two weeks. This increased processing capacity is realized .without deleterious changes in photographic quality during this period. The normal reduction in developing activity due to aerial oxidation and exhaustion is counterbalanced in our system by .withholding a part of the thiosulfate content in the form of silver thiosulfate complex. When the complex is evcnt ually destroyed, re-entry of the thiosulfate causes severe degradation of the developed image. This effect does not occur when processed with our novel monobath compositions. 7
It has also been found that the developing rate of our novel monobaths can be accelerated by adding a small quantity of a water-soluble hydroxyalkylamine compound. Moreover, such hydroxyalkylamine compounds frequently give improved solution life and greater image stabilityJ Typical hydroxyalkylamine compounds useful in our invention include ethanolamine, 2,2'-irninodiethanol, 2,2,2"-nitrilotriethanol -(triethanolamine), N-monomethylethanolamine, N-monoethylethanolamine, N,N-dimethylethanolamine, N,N-diethylethanolamine, etc. Particularly useful hydroxyalkylamines include those represented by the following general formula:
wherein R and R each represents a hydrogen atom, a lower alkyl radical (e.g., methyl, ethyl, propyl, etc), or a hydroxyalkyl radical (e.g., fi-hydroxyethyl, [3-hydroxypropyl, etc.).
A particularly useful monobath composition was prepared according to the method described in Example 1 above by including about 9 grams of ethanolamine in the composition. The combination of the mercaptotetrazole compound and the ethanolamine compound gave particularly useful results, insofar as freedom from sludge and development speed were concerned. Excellent photographic quality was obtained using such combinations. The amount of hydroxyalkyl compound used can be varied. We have found that from about 5 to 20 grams per liter give quite useful effects.
The invention has been described in detail with particular reference to preferred embodiments thereof, but it will be understood that variations and modifications can be efiected within the spirit and scope of the invention as described hereinabove and as defined in the appended claims.
What we claim as our invention and desire secured by Letters Patent of the United States is:
l. A monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thiosulfate, a Water-soluble hydroxyalkylamine, and from about 0.001 to about 1.0 gram per liter of solution of a heterocyclic mercaptan capable of adsorbing silver compounds formed by photographic development to solubilize such silver compounds, said heterocyclic mercaptan being selected from the class consisting of mercaptotetrazoles, mercapto-1,3,4-oxadiazoles and mercapto-1,3,4-thiadiazoles.
2. A monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thiosulfate, and from about 0.001 to about 10 gram per liter of a water-soluble heterocyclic mercaptan which renders silver containing precipitating nuclei soluble upon adsorption of said mercaptan thereto, said heterocyclic mercaptan being selected from the class consisting of mercaptotetrazoles, mercapto-1,3,4-oxadiazoles and mercapto- 1,3,4-thiadiazoles.
3. A monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thiosulfate, and from about 0.001 to about 1.0 gram per liter of 1- phenyl-S-mercaptotetrazole.
4. A monobath composition according to claim 3 wherein said silver halide developing agent is a 3-pyrazolidone.
5. A monobath composition for simultaneously developing andfixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thiosulfate, and from about 0.001 to about 1.0 gram per liter of 2- mercapto-S-o-hydroxyphenyl-1,3,4-thiadiazole.
6. A monobath composition as defined in claim 5 wherein said silver halide developing agent is a S-pyrazolidone.
7. A monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least grams per liter of solution of a water-soluble thiosulfate, and from about 0.001 to about 1.0 gram per liter of 2- mercapto-S-o-tolyl-1,3,4-oxadiazole.
8. A monobath composition as defined in claim 7 wherein said silver halide developing agent is a 3-pyrazolidone.
9. A monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thiosulfate, and from about 0.001 to about 1.0 gram per liter of 2- mercapto-5-phenyl-1,3,4-oxadiazole.
10. A monobath composition as defined in claim 9 wherein said silver halide developing agent is a 3- pyrazolidone.
11. A monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a Water-soluble thiosulfate, and from about 0.001 to about 1.0 gram per liter of Z-mercapto-S-p-nitrophenyl-1,3,4-oxadiazole.
12. A monobath composition as defined in claim 11 wherein said silver halide developing agent is a 3- pyrazolidone.
13. A monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thiosulfate, and from about 0.001 to about 1.0 gram per liter of Z-mercapto-S-cyclohexyl-1,3,4-thiadiazole.
14. A monobath composition as defined in claim 13 wherein said silver halide developing agent is a 3- pyrazolidone.
15. A monobath composition for simultaneously developing and fixing an exposed photographic silver halide emulsion layer comprising an aqueous alkaline solution of a photographic silver halide developing agent for reducing exposed silver halide to metallic silver, at least 80 grams per liter of solution of a water-soluble thicsulfate, and from about 0.001 to about 1.0 gram per liter of 2-mercapto-S-m-nitrophenyl-1,3,4-oxadiazole.
16. A monobath composition as defined in claim 15 wherein said silver halide developing agent is a 3- pyrazolidone.
17. In a method of processing in a continuous fashion large quantities of exposed photographic silver halide emulsion layers coated on a paper support by developing said emulsion layers in a monobath composition containing a photognaphic silver halide developing agent for reducing exposed silver halide to metallic silver and at least 80 grams per liter of solution of a water-soluble thiosulfate, the improvement comprising adding to said monobath from about 0.001 to about 1.0 gram per liter of solution of a heterocyclic mercaptan selected from the class consisting of 1-phenyl-S-mercaptotetrazole, 2-mercapto-S-o-hydroxyphenyl-1,3,4-thiadiazole, 2-mercapto-5- o-tolyl-1,3,4-oxadiazole, Z-mercapto-S-phenyl-l,3,4-oxadiazole, Z-mer-capto-5-p-nitrophenyl-1,3,4-oxadiazole, 2-
7 3 mercapto-S-cycildhexyl-l,3,4-thiadiazole, and 'Z-mercapto- 3,130,155 Ya ckel 'et a1 Feb. 2, 1962 5-.m-;nitrophcnyl-1,3,4oxadiazole. 3,063,837 Lassig et al. Nov. 13, 1962 18. In a .process according 'to claim 17, the improvement comprising adding a small quantity of a water- FOREIGN PATENTS soluble:hydro-xyalkylamine to said monobath. V 5 573,105 Great Britain 6, 1945 973,818 Gcarnany June 15, 1960 References Cited in 'the file of this patent 7 OTHER REFERENCES UNITED STATES PATENTS Newman: Seventy Years of Progress in Photographic 2,453,346 Russell Nov. 9, 1948 Monob aths, The British Journal of Photography, Jan. 2,699,393 Weyde Tan. 11, 1955 23, 1959, pp. 44-58.
Claims (1)
1. A MONOBATH COMPOSTION FOR SIMULTANEOUSLY DEVELOPING AND FIXING AN EXPOSED PHTOGRAPHIC SILVER HALIDE EMULSION LAYER COMPRISING AN AQUEOUS ALKALINE SOLUTION OF A PHOTOGRAPHIC SILVER HALIDE DEVELOPING AGENT FOR REDUCING EXPOSED SILVER HALIDE TO METALLIC SILVER, AT LEAST 80 GRAMS PER LITER OF SOLUTION OF A WATER-SOLUBLE THIOSULFATE, A WATER-SOLUBLE HYDROXYALKYLAMINE, AND FROM ABOUT 0.001 TO ABOUT 1.0 GRAM PER LITER OF SOLUTION OF A HETEROCYCLIC MERCAPTAN CAPABLE OF ADSORBING SILVER COMPOUNDS FORMED BY PHOTOGRAPHIC DEVELOPMENT TO SOLUBILIZE SUCH SILVER COMPOUNDS, SAID HETEROCYCLIC MERCAPTAN BEING SELECTED FROM THE CLASS CONSISTING OF MERCAPTOTETRAXOLES, MERCAPTO-1,3,4-OXADIAZOLES AND MERCAPTO-1,3,4-THIADIAZOLES.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US169668A US3173789A (en) | 1962-01-29 | 1962-01-29 | Method and composition for inhibiting silver sludge in thiosulfate monobaths |
| GB3162/63A GB1030442A (en) | 1962-01-29 | 1963-01-25 | Photographic monobath compositions |
| FR922833A FR1345516A (en) | 1962-01-29 | 1963-01-28 | Development-fixing bath avoiding the formation of silver sludge |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US169668A US3173789A (en) | 1962-01-29 | 1962-01-29 | Method and composition for inhibiting silver sludge in thiosulfate monobaths |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3173789A true US3173789A (en) | 1965-03-16 |
Family
ID=22616666
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US169668A Expired - Lifetime US3173789A (en) | 1962-01-29 | 1962-01-29 | Method and composition for inhibiting silver sludge in thiosulfate monobaths |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US3173789A (en) |
| GB (1) | GB1030442A (en) |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3318701A (en) * | 1964-10-21 | 1967-05-09 | Technical Operations Inc | Photographic monobaths containing a dl 6-8 dithio-octanoic acid antisludging agent |
| US3390998A (en) * | 1965-10-04 | 1968-07-02 | Eastman Kodak Co | Stabilized physical developers |
| US3392019A (en) * | 1963-04-08 | 1968-07-09 | Eastman Kodak Co | Viscous silver halide photographid monobath solutions |
| US3542554A (en) * | 1967-11-30 | 1970-11-24 | Eastman Kodak Co | Mercapto-substituted hydroquinone developing agents |
| US3769015A (en) * | 1969-08-18 | 1973-10-30 | Mitsubishi Paper Mills Ltd | Developer monobath free from formation of colored sludge |
| US4371610A (en) * | 1980-07-24 | 1983-02-01 | Fuji Photo Film Co., Ltd. | Process for development-processing silver halide light-sensitive material |
| JPS6173950A (en) * | 1984-09-20 | 1986-04-16 | Mitsubishi Paper Mills Ltd | Processing solution for silver complex diffusion transfer |
| US5188662A (en) * | 1991-06-28 | 1993-02-23 | Eastman Kodak Company | Silver recovery process |
| US5210009A (en) * | 1991-06-28 | 1993-05-11 | Eastman Kodak Company | Silver recovery element and process |
| JPH05249623A (en) * | 1991-03-19 | 1993-09-28 | Fuji Photo Film Co Ltd | Development processing method for silver halde photographic sensitive material |
| US5310629A (en) * | 1991-06-28 | 1994-05-10 | Eastman Kodak Company | Silver recovery element and method |
| US5660972A (en) * | 1994-03-16 | 1997-08-26 | Mitsubishi Paper Mills Limited | Method for photographic development using a filter to inhibit occurrence of silver sludges |
| EP0834768A1 (en) | 1996-10-02 | 1998-04-08 | Konica Corporation | Method for processing silver halide photographic light-sensitive material |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59188641A (en) | 1983-04-11 | 1984-10-26 | Fuji Photo Film Co Ltd | Silver halide photographic emulsion |
| EP2619628B1 (en) | 2010-09-17 | 2014-03-26 | Fujifilm Manufacturing Europe BV | Photographic paper and its use in a photo album |
| GB202006061D0 (en) | 2020-04-24 | 2020-06-10 | Fujifilm Mfg Europe Bv | Photographic paper |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB573105A (en) * | 1943-11-26 | 1945-11-06 | Leonard Vincent Chilton | Improvements in or relating to photographic materials |
| US2453346A (en) * | 1945-10-25 | 1948-11-09 | Eastman Kodak Co | Stabilization of processed photographic emulsions to high temperatures and humidities |
| US2699393A (en) * | 1950-04-15 | 1955-01-11 | Agfa Ag Fur Photofabrikation | Photographic process for the direct production of positive images |
| DE973818C (en) * | 1953-07-18 | 1960-06-15 | Leonar Werke Ag | Process for the production of photographic images by simultaneously developing and fixing or stabilizing exposed halide silver layers by means of a developer substance and a fixing or stabilizing agent and optionally an alkali sulfite and / or an alkali-containing solution |
| US3020155A (en) * | 1956-05-23 | 1962-02-06 | Eastman Kodak Co | Photographic diffusion transfer process |
| US3063837A (en) * | 1958-11-07 | 1962-11-13 | Agfa Ag | Photographic diffusion transfer process for planographic printing |
-
1962
- 1962-01-29 US US169668A patent/US3173789A/en not_active Expired - Lifetime
-
1963
- 1963-01-25 GB GB3162/63A patent/GB1030442A/en not_active Expired
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB573105A (en) * | 1943-11-26 | 1945-11-06 | Leonard Vincent Chilton | Improvements in or relating to photographic materials |
| US2453346A (en) * | 1945-10-25 | 1948-11-09 | Eastman Kodak Co | Stabilization of processed photographic emulsions to high temperatures and humidities |
| US2699393A (en) * | 1950-04-15 | 1955-01-11 | Agfa Ag Fur Photofabrikation | Photographic process for the direct production of positive images |
| DE973818C (en) * | 1953-07-18 | 1960-06-15 | Leonar Werke Ag | Process for the production of photographic images by simultaneously developing and fixing or stabilizing exposed halide silver layers by means of a developer substance and a fixing or stabilizing agent and optionally an alkali sulfite and / or an alkali-containing solution |
| US3020155A (en) * | 1956-05-23 | 1962-02-06 | Eastman Kodak Co | Photographic diffusion transfer process |
| US3063837A (en) * | 1958-11-07 | 1962-11-13 | Agfa Ag | Photographic diffusion transfer process for planographic printing |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3392019A (en) * | 1963-04-08 | 1968-07-09 | Eastman Kodak Co | Viscous silver halide photographid monobath solutions |
| US3318701A (en) * | 1964-10-21 | 1967-05-09 | Technical Operations Inc | Photographic monobaths containing a dl 6-8 dithio-octanoic acid antisludging agent |
| US3390998A (en) * | 1965-10-04 | 1968-07-02 | Eastman Kodak Co | Stabilized physical developers |
| US3542554A (en) * | 1967-11-30 | 1970-11-24 | Eastman Kodak Co | Mercapto-substituted hydroquinone developing agents |
| US3769015A (en) * | 1969-08-18 | 1973-10-30 | Mitsubishi Paper Mills Ltd | Developer monobath free from formation of colored sludge |
| US4371610A (en) * | 1980-07-24 | 1983-02-01 | Fuji Photo Film Co., Ltd. | Process for development-processing silver halide light-sensitive material |
| JPS6173950A (en) * | 1984-09-20 | 1986-04-16 | Mitsubishi Paper Mills Ltd | Processing solution for silver complex diffusion transfer |
| JPH05249623A (en) * | 1991-03-19 | 1993-09-28 | Fuji Photo Film Co Ltd | Development processing method for silver halde photographic sensitive material |
| JP2684257B2 (en) | 1991-03-19 | 1997-12-03 | 富士写真フイルム株式会社 | Developing method of silver halide photographic material |
| US5188662A (en) * | 1991-06-28 | 1993-02-23 | Eastman Kodak Company | Silver recovery process |
| US5210009A (en) * | 1991-06-28 | 1993-05-11 | Eastman Kodak Company | Silver recovery element and process |
| US5310629A (en) * | 1991-06-28 | 1994-05-10 | Eastman Kodak Company | Silver recovery element and method |
| US5660972A (en) * | 1994-03-16 | 1997-08-26 | Mitsubishi Paper Mills Limited | Method for photographic development using a filter to inhibit occurrence of silver sludges |
| EP0834768A1 (en) | 1996-10-02 | 1998-04-08 | Konica Corporation | Method for processing silver halide photographic light-sensitive material |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1030442A (en) | 1966-05-25 |
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