US3615507A - Photographic bleach-fix solutions - Google Patents
Photographic bleach-fix solutions Download PDFInfo
- Publication number
- US3615507A US3615507A US783750A US3615507DA US3615507A US 3615507 A US3615507 A US 3615507A US 783750 A US783750 A US 783750A US 3615507D A US3615507D A US 3615507DA US 3615507 A US3615507 A US 3615507A
- Authority
- US
- United States
- Prior art keywords
- bleach
- fix
- iodine
- silver
- solution
- 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
- 239000004332 silver Substances 0.000 claims abstract description 47
- 229910052709 silver Inorganic materials 0.000 claims abstract description 47
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 38
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 38
- 239000011630 iodine Substances 0.000 claims abstract description 38
- 239000007800 oxidant agent Substances 0.000 claims abstract description 23
- 230000001590 oxidative effect Effects 0.000 claims abstract description 22
- -1 silver ions Chemical class 0.000 claims description 30
- 238000000034 method Methods 0.000 claims description 26
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 22
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 150000002500 ions Chemical class 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical group [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 150000002009 diols Chemical group 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 238000013019 agitation Methods 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- 239000000203 mixture Substances 0.000 abstract description 13
- JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 abstract description 12
- 229910021612 Silver iodide Inorganic materials 0.000 abstract description 12
- 229940045105 silver iodide Drugs 0.000 abstract description 12
- 230000008929 regeneration Effects 0.000 abstract description 5
- 238000011069 regeneration method Methods 0.000 abstract description 5
- 238000006243 chemical reaction Methods 0.000 abstract description 4
- 239000002244 precipitate Substances 0.000 abstract description 4
- 239000000243 solution Substances 0.000 description 52
- 239000010410 layer Substances 0.000 description 16
- 239000000463 material Substances 0.000 description 15
- 238000004061 bleaching Methods 0.000 description 12
- 239000007844 bleaching agent Substances 0.000 description 8
- 230000001172 regenerating effect Effects 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 150000002430 hydrocarbons Chemical group 0.000 description 5
- 230000018109 developmental process Effects 0.000 description 4
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- YAGKRVSRTSUGEY-UHFFFAOYSA-N ferricyanide Chemical compound [Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] YAGKRVSRTSUGEY-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 229910001961 silver nitrate Inorganic materials 0.000 description 2
- 239000011593 sulfur Chemical group 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- PVMURSYOQVEKJP-UHFFFAOYSA-N 1-ethylimidazolidine-2-thione Chemical compound CCN1CCNC1=S PVMURSYOQVEKJP-UHFFFAOYSA-N 0.000 description 1
- FDDDTDSPQXLQFY-UHFFFAOYSA-N 1-methylimidazolidine-2-thione Chemical compound CN1CCNC1=S FDDDTDSPQXLQFY-UHFFFAOYSA-N 0.000 description 1
- HRBLHUVHOWWBEN-UHFFFAOYSA-N 1-n,4-n-diethylbenzene-1,4-diamine;hydrochloride Chemical compound Cl.CCNC1=CC=C(NCC)C=C1 HRBLHUVHOWWBEN-UHFFFAOYSA-N 0.000 description 1
- PXJHVKRLFWZUNV-UHFFFAOYSA-N 1-n,4-n-dimethylbenzene-1,4-diamine;hydron;dichloride Chemical compound Cl.Cl.CNC1=CC=C(NC)C=C1 PXJHVKRLFWZUNV-UHFFFAOYSA-N 0.000 description 1
- AFBBKYQYNPNMAT-UHFFFAOYSA-N 1h-1,2,4-triazol-1-ium-3-thiolate Chemical compound SC=1N=CNN=1 AFBBKYQYNPNMAT-UHFFFAOYSA-N 0.000 description 1
- SUVZGLSQFGNBQI-UHFFFAOYSA-N 2,5-bis(sulfanyl)hexanedioic acid Chemical compound OC(=O)C(S)CCC(S)C(O)=O SUVZGLSQFGNBQI-UHFFFAOYSA-N 0.000 description 1
- RMMPZDDLWLALLJ-UHFFFAOYSA-N 2,5-dimethoxy-1,4-benzoquinone Natural products COC1=CC(=O)C(OC)=CC1=O RMMPZDDLWLALLJ-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- DLLMHEDYJQACRM-UHFFFAOYSA-N 2-(carboxymethyldisulfanyl)acetic acid Chemical compound OC(=O)CSSCC(O)=O DLLMHEDYJQACRM-UHFFFAOYSA-N 0.000 description 1
- NJIAMNMXCYGBOW-UHFFFAOYSA-N 2-[2-[2-(carboxymethylsulfanyl)ethylsulfanyl]ethylsulfanyl]acetic acid Chemical compound OC(=O)CSCCSCCSCC(O)=O NJIAMNMXCYGBOW-UHFFFAOYSA-N 0.000 description 1
- WOGWYSWDBYCVDY-UHFFFAOYSA-N 2-chlorocyclohexa-2,5-diene-1,4-dione Chemical compound ClC1=CC(=O)C=CC1=O WOGWYSWDBYCVDY-UHFFFAOYSA-N 0.000 description 1
- VTWDKFNVVLAELH-UHFFFAOYSA-N 2-methylcyclohexa-2,5-diene-1,4-dione Chemical compound CC1=CC(=O)C=CC1=O VTWDKFNVVLAELH-UHFFFAOYSA-N 0.000 description 1
- ZIUZDRMIXJKUNY-UHFFFAOYSA-N 3-[2-carboxyethyl(ethyl)amino]propanoic acid Chemical compound OC(=O)CCN(CC)CCC(O)=O ZIUZDRMIXJKUNY-UHFFFAOYSA-N 0.000 description 1
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 1
- IJJSFSXLZYFTKV-UHFFFAOYSA-N 4-n-methylbenzene-1,4-diamine;hydrochloride Chemical compound Cl.CNC1=CC=C(N)C=C1 IJJSFSXLZYFTKV-UHFFFAOYSA-N 0.000 description 1
- 229910021581 Cobalt(III) chloride Inorganic materials 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- QEVGZEDELICMKH-UHFFFAOYSA-N Diglycolic acid Chemical compound OC(=O)COCC(O)=O QEVGZEDELICMKH-UHFFFAOYSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- MPLZNPZPPXERDA-UHFFFAOYSA-N [4-(diethylamino)-2-methylphenyl]azanium;chloride Chemical compound [Cl-].CC[NH+](CC)C1=CC=C(N)C(C)=C1 MPLZNPZPPXERDA-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910001513 alkali metal bromide Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- JAWGVVJVYSANRY-UHFFFAOYSA-N cobalt(3+) Chemical compound [Co+3] JAWGVVJVYSANRY-UHFFFAOYSA-N 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000011365 complex material Substances 0.000 description 1
- 229960003280 cupric chloride Drugs 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229960001484 edetic acid Drugs 0.000 description 1
- FXDWOKJYEDVJME-UHFFFAOYSA-N ethene;2-sulfanylacetic acid Chemical compound C=C.OC(=O)CS.OC(=O)CS FXDWOKJYEDVJME-UHFFFAOYSA-N 0.000 description 1
- UKFXDFUAPNAMPJ-UHFFFAOYSA-N ethylmalonic acid Chemical compound CCC(C(O)=O)C(O)=O UKFXDFUAPNAMPJ-UHFFFAOYSA-N 0.000 description 1
- 229910001447 ferric ion Inorganic materials 0.000 description 1
- VEPSWGHMGZQCIN-UHFFFAOYSA-H ferric oxalate Chemical compound [Fe+3].[Fe+3].[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O VEPSWGHMGZQCIN-UHFFFAOYSA-H 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- SUBFIBLJQMMKBK-UHFFFAOYSA-K iron(3+);trithiocyanate Chemical compound [Fe+3].[S-]C#N.[S-]C#N.[S-]C#N SUBFIBLJQMMKBK-UHFFFAOYSA-K 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Chemical group 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000012089 stop solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- JFSUDVTVQZUDOP-UHFFFAOYSA-N tetrasodium;iron(2+);hexacyanide;decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[Na+].[Na+].[Fe+2].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] JFSUDVTVQZUDOP-UHFFFAOYSA-N 0.000 description 1
- YARHBRUWMYJLHY-UHFFFAOYSA-Q triazanium;iron(3+);hexacyanide Chemical compound [NH4+].[NH4+].[NH4+].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] YARHBRUWMYJLHY-UHFFFAOYSA-Q 0.000 description 1
- DCXPBOFGQPCWJY-UHFFFAOYSA-N trisodium;iron(3+);hexacyanide Chemical compound [Na+].[Na+].[Na+].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCXPBOFGQPCWJY-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
- G03C5/395—Regeneration of photographic processing agents other than developers; Replenishers therefor
- G03C5/3952—Chemical, mechanical or thermal methods, e.g. oxidation, precipitation, centrifugation
Definitions
- compositions which are effective as photographic bleach-fixes can be prepared from solutions containing substantial amounts of reduced oxidant, e.g., ferrocyanide, and dissolved silver by reaction with iodine which oxidizes the reduced oxidant and precipitates silver as silver iodide This can be used for effective regeneration of photographic bleachfix compositions.
- reduced oxidant e.g., ferrocyanide
- This invention relates to photographic processing. In one aspect this invention relates to combined bleach and fix solutions commonly known as bleach-fix solutions. in another aspect this invention relates to methods for regenerating bleach-fix solutions.
- Combined bleach-fix compositions are used in processing of silver halide color photographic materials after color development to convert metallic silver to its cationic state (bleaching) and to dissolve otherwise insoluble silver salts from the photographic element (fixing).
- the combination of the bleaching and fixing operations into a single step simplifies processing and processing machines and decreases processing time thereby offering potential cost savings in processing and also in solution storage and handling.
- this invention provides methods for regenerating bleach-fixes whereby costs associated with the use of bleach-fix solutions can be substantially decreased.
- This invention also provides regenerated bleach-fixes and methods for using these bleach-fixes in the processing of silver halide color photographic materials.
- this invention provides simple methods for removing silver from used bleach-fixes containing complexed silver ions and reduced oxidant while substantially simultaneously oxidizing the reduced oxidant thereby regenerating the bleach-fix, i.e., restoring substantially all of the original bleaching and fixing capabilities of the bleach-fix.
- iodine is combined with an exhausted bleach-fix solution, that is, a combined bleaching and fixing solution, which has been used to such an extent that it no longer reliably performs both its bleaching and fixing function or a combined bleaching and fixing solution which contains substantial amounts of reduced bleaching agent (oxidant) and substantial amounts of dissolved silver ions.
- the iodine can, for example, be added as a solid, a gas, or advantageously as a solution desirably in a water immiscible solvent.
- the amount of iodine used will depend to some degree of the type of bleach-fix, the extent the bleach-fix has been used, the type of photographic material processed, etc.
- a weight of iodine somewhat in excess of the calculated weight of ionized silver present in the solution.
- the amount of iodine added is desirably no greater than about l.2 g. iodine per gram of silver present in the solution and advantageously no greater than about l.l8 g. iodine per gram of silver present in the solution.
- Lesser quantities of iodine may be desirable but usually only result in bleach-fix solutions which are not completely regenerated unless, of course, some halide has previously been generated or used in the bleach-fix itself.
- the time necessary for the regeneration varies widely.
- the reaction takes somewhat longer than when the iodine is added as a solution in a nonwater miscible solvent, such as benzene or chloroform.
- a nonwater miscible solvent such as benzene or chloroform.
- water miscible solvents may be employed provided they do not deleteriously affect the basic character of the bleach-fix.
- the temperature for the regeneration step also may vary with the upper limits determined to a large degree by the stability of the bleaching and fixing agents selected.
- the combined stable bleaching and fixing solution can be prepared by combining a number of silver bleaching agents, i.e., materials which oxidize silver to silver ions and silver halide fixing agents, i.e., so-called silver halide solvents.
- silver bleaching agents i.e., materials which oxidize silver to silver ions
- silver halide fixing agents i.e., so-called silver halide solvents.
- the bleaching agents or oxidants, used in the combined bleaching and fixing solutions according to the present invention have a reduced state sufficiently stable that degradation will not occur but which can be oxidized to the original state, that is, as it existed in a fresh bleach-fix, by reaction with molecular iodine.
- oxidants effective in combined bleaches and fixes are those metals which have ions of multiple oxidation states, for example, cupric ions (supplied to the solution as water soluble salts, such as cupric chloride, nitrate, sulfate, etc.); cob'altic ions (supplied to the solution as water soluble salts, such as cobaltic chloride, cobaltic ammonium nitrate, etc.); and especially ferric ions (supplied to the solution as a simple water-soluble ferric salt, e.g., ferric chloride, ferric nitrate, ferric thiocyanate, ferric oxalate, etc.
- cupric ions supplied to the solution as water soluble salts, such as cupric chloride, nitrate, sulfate, etc.
- cob'altic ions supplied to the solution as water soluble salts, such as cobaltic chloride, cobaltic ammonium nitrate, etc.
- ferric ions supplied to
- bleaching agents include water-soluble quinones (e.g., quinone, sulfophenylquinone, chloroquinone, methoxyquinone, 2,5-dimethoxyquinone, methylquinone, etc.); complex salts of an alkali metal and a polyvalent cation with an organic acid having one of the formulas:
- R, R", R, R", and R" each represent a substitutedhydrocarbon residue and an unsubstituted hydrocarbon residue
- R represents hydrogen, an unsubstituted hydrocarbon residue and a substituted hydrocarbon residue
- the polyvalent cation is selected from the class of ferric ion, cobaltic ion and cupric ions.
- the organic acids are ethylene diamine tetraacetic acid, nitrilotriacetic acid, malonic acid, ethyl malonic acid, tartaric acid, maleic acid, fumaric acid, diglycolic acid, ethyliminodipropionic acid, ethylene dithioglycolic acid, dithioglycolic acid, etc.
- the reduced oxidant contains a ferrous moiety.
- the fixing agents, or silver halide solvents, utilized in the present invention include those fixing agents which do not dissolve an appreciable quantity of silver iodide usually less than a few grams per liter, ideally less than one-half gram per liter.
- Highly suitable fixing agents are water-soluble organic diol fixing agents containing sulfur atoms interspersed along the carbon chain (e.g., 3-thia-l-5-pentanediol, 3,6-dithia-l,8-octanediol,3 ,6,9-trithial ,l l-undecanediol,3 ,6, 9, l Ztetrathia-I l4-tetradecanediol, 9-oxa-3 ,6,9,12,l5-tretathial ,17-heptadecanediol, 3,6,9,l2,2l,30,33,36,39-nonaoxa-l5,l8,24,27
- water-soluble sulfur-containing organic dibasic-acids which are especially useful, e.g., ethylene bis-thioglycolic acid, 3,6,9-trithiahendecanedioic acid, 3,6,9,lZ-tetrathiatetradecanedioic acid and their water-soluble salts (e.g., sodium salts, potassium salts, etc.), an imidazolidinthione (e.g., methyl imidazolidinthione, ethyl imidazolidinthione, etc. etc.
- Addenda commonly used in bleach-fix solutions may be used in bleach-fixes which can be regenerated according to the present invention including phosphates, alkali metal bromide, ammonium bromide, amines, mercapto derivatives of 5- membered heterocyclic rings, such as mercaptotriazole, etc.
- the pH of the solution is usually maintained at about 7 or desirably at about 6.8, slightly on the acid side of neutral.
- iodine is added to a combined bleaching and fixing solution which has been utilized in processing photographic materials having colorforming couplers contained in respective layers of a multilayer photographic element.
- Materials of this type have been described in a number of U.S. and foreign patents, for example, in U.S. Patents 2,322,027, June 15, 1943; 2,407,210, Sept. 3, 1946; 2,474,293, June 28, 1949; 2,640,776, June 2, 1953; and 2,956,876, Oct. 18, 1960. Included are the socalled negative-positive type materials as well as reversal materials.
- the photographic multilayer color materials comprise elements having usually three selectively sensitive emul sion layers coated on one side of a photographic support.
- Sensitive layers of the elements contain color-forming couplers to form the complementary dye to which a particular layer is sensitive.
- the uppermost layer can be blue-sensitive and normally incorporates a yellowforming coupler.
- the next layer generally comprises a filter layer which is yellow in color and blue absorbing and being placed under the top layer absorbs most of the blue light thus preventing unwanted blue exposure below the filter layer.
- the next layer is generally green-sensitive and usually incorporates a magenta-dye forming coupler.
- the emulsion layer adjacent to the support is then red-sensitive and according to the present invention normally contains a cyan-dye forming coupler.
- multilayer photographic elements used in the present invention contain additional silver halide emulsion layers or other interlayers for specialized purposes. In photographic print materials, frequently the yellow filter layer is omitted and the arrangement of silver halide emulsion layers may be changed for the purpose of obtaining more accurate recording of the color negative.
- any color-forming developer containing a primary amino group may be used.
- These compounds are usually used in the salt form, such as the hydrochloride or the sulfate which are more stable than the amines themselves.
- Suitable compounds are diethyl-p-phenylenediamine hydrochloride, monomethylp-phenylenediamine hydrochloride, dimethyl-p-phenylenediamine hydrochloride, and 2-amino-5- diethylaminotoluene hydrochloride.
- the p-amino phenols and their substitution products may also be used where the amino group is unsubstituted. All of these developers have an unsubstituted amino group which enables the oxidation products of the developer to couple with the color-forming compounds to form a dye image.
- the processing procedure usually comprises the following steps:
- the regenerated bleach-fixes of the present invention are utilized in processing of reversal photographic materials in which the color development is preceded by a black and white development step which, of course, involves well-known black and white developers, e.g., hydroquinone type.
- iodine in the indicated manner results in a method for regenerating photographic bleach-fix compositions or to restore to a used bleach-fix a substantial amount of the bleaching and fixing capabilities which it exhibited as a fresh bleach-fix, which method comprises a. combining (admixing), desirably with agitation or stirring, a bleach-fix containing: i. substantial amounts of reduced oxidant, advantageously ferrocyanide ions; and ii.
- silver ions which in one advantageous embodiment are rendered soluble by the presence of organic diols or diacid functional groups having one or more -S-" moieties interspersed in a hydrocarbon chain separating the functional groups, highly efiicacious examples of which are 2,2- ethylenedithiadiethanol, thiadiethanol, and 2,2- ethylenedithiaacetic acid; with iodine, desirably by adding iodine as a solid or advantageously dissolved in water immiscible solvent to the bleach-fix and mixing for a sufficient period of time to allow the iodine to convert reduced oxidant to its oxidized state, e.g., ferrocyanide to ferricyanide, with the iodide formed thereby precipitating as silver iodide; and
- the reaction mixture is vigorously agitated for about 2 minutes.
- a precipitate of silver iodide is formed which is removed by filtration.
- the amount of silver halide that is removed corresponds to the removal of about 0.45 g. silver.
- the treated solution functions surprisingly effectively as a bleach-fix for use in processing photographic materials as described hereinabove, especially with reversal color photographic materials which are processed in a conventional manner except for the use of the treated bleach-fix in lieu of a fresh bleach-fix.
- the ferrocyanide was stoichiometrically oxidized by the iodine to ferricyanide.
- EXAMPLE 2 The procedure of example 1 is followed except that 1.18 g. iodine is added instead of 0.6 g. The quantity of silver removed as silver halide is about 0.9 g. The treated solution functions as a bleach-fix in a manner and to an extent analogous to that of example 1.
- EXAMPLE 3 The procedure of example 1 is followed except that about 1.8 g. iodine is added instead of 0.6 g. The silver is removed quantitatively as silver iodide. The regenerated solution is effective in its bleaching capacity but less satisfactory in capacity as a fixing solution when compared to that of example 1.
- EXAMPLE 4 The procedure according to example 4 is followed except that about 5.9 g. iodine is added to a liter of solution and about 4.7 g. silver is precipitated as silver iodide.
- the regenerated bleach-fix is as effective as that of example 1.
- EXAMPLE 7 The procedure according to example 1 is followed except that 2,2'-ethylenedithiadiacetic acid is used in lieu of 2,2- ethylenedithiadiethanol. Results similar to example l are achieved.
- EXAMPLE 8 The procedure according to example 1 is followed except that 200 ml. (about C.) thiadiethanol is used in lieu of 70 g. 2,2-ethylenedithiadiethanol. Results analogous to example 1 are achieved.
- EXAMPLE 9 The procedure according to example 8 is followed except that 8 g. silver nitrate are used to produce a simulated seasoned bleach containing 5 g. dissolved silver per liter of solution. The addition of 5 g. iodine resulted in the precipitation of about 3.9 g. silver as silver iodide. Also, ferrocyanide is oxidized by iodine stoichiometrically to ferricyanide. The
- EXAMPLE 10 A photographic bleach-fix composition containing dissolved silver and ferrocyanide and other materials in quantities generally analogous to the ingredients indicated in example 5 but silver ions resulting from the use of the solution as a bleach-fix composition is treated in accordance with the procedures outlined in example 5. Results similar to those of example 5 are achieved.
- step (a) is accompanied by vigorous agitation and iodine is added to the bleach-fix as crystalline iodine.
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Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US78375068A | 1968-12-13 | 1968-12-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3615507A true US3615507A (en) | 1971-10-26 |
Family
ID=25130284
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US783750A Expired - Lifetime US3615507A (en) | 1968-12-13 | 1968-12-13 | Photographic bleach-fix solutions |
Country Status (6)
Country | Link |
---|---|
US (1) | US3615507A (enrdf_load_stackoverflow) |
BE (1) | BE742943A (enrdf_load_stackoverflow) |
DE (1) | DE1961997A1 (enrdf_load_stackoverflow) |
FR (1) | FR2026061A1 (enrdf_load_stackoverflow) |
GB (1) | GB1229077A (enrdf_load_stackoverflow) |
SE (1) | SE352967B (enrdf_load_stackoverflow) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3772194A (en) * | 1972-06-21 | 1973-11-13 | Eastman Kodak Co | Silver catalyzed oxidation of complex metal cyanides |
US3839043A (en) * | 1972-04-27 | 1974-10-01 | Agfa Gevaert Ag | Process for regenerating spent photographic silver bleaching solutions |
US3904412A (en) * | 1972-10-04 | 1975-09-09 | Agfa Gevaert Nv | Method for the preparation of planographic printing plates from silver images |
US5633124A (en) * | 1992-05-08 | 1997-05-27 | Eastman Kodak Company | Acceleration of silver removal by thioether compounds |
US5716766A (en) * | 1995-05-18 | 1998-02-10 | Fuji Photo Film Co., Ltd. | Method and apparatus for the electrolytic treatment of bleach-fix baths, as well as an apparatus for processing photographic materials |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1269260A4 (en) * | 2000-01-06 | 2003-06-25 | Trebla Chemical Company | ONE-PIECE CONCENTRATE OF A WHITE FIXING SOLUTION |
-
1968
- 1968-12-13 US US783750A patent/US3615507A/en not_active Expired - Lifetime
-
1969
- 1969-12-10 BE BE742943D patent/BE742943A/xx unknown
- 1969-12-10 FR FR6942650A patent/FR2026061A1/fr not_active Withdrawn
- 1969-12-10 DE DE19691961997 patent/DE1961997A1/de active Pending
- 1969-12-12 GB GB1229077D patent/GB1229077A/en not_active Expired
- 1969-12-15 SE SE17294/69A patent/SE352967B/xx unknown
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3839043A (en) * | 1972-04-27 | 1974-10-01 | Agfa Gevaert Ag | Process for regenerating spent photographic silver bleaching solutions |
US3772194A (en) * | 1972-06-21 | 1973-11-13 | Eastman Kodak Co | Silver catalyzed oxidation of complex metal cyanides |
US3904412A (en) * | 1972-10-04 | 1975-09-09 | Agfa Gevaert Nv | Method for the preparation of planographic printing plates from silver images |
US5633124A (en) * | 1992-05-08 | 1997-05-27 | Eastman Kodak Company | Acceleration of silver removal by thioether compounds |
US5716766A (en) * | 1995-05-18 | 1998-02-10 | Fuji Photo Film Co., Ltd. | Method and apparatus for the electrolytic treatment of bleach-fix baths, as well as an apparatus for processing photographic materials |
Also Published As
Publication number | Publication date |
---|---|
DE1961997A1 (de) | 1970-06-25 |
SE352967B (enrdf_load_stackoverflow) | 1973-01-15 |
GB1229077A (enrdf_load_stackoverflow) | 1971-04-21 |
FR2026061A1 (enrdf_load_stackoverflow) | 1970-09-11 |
BE742943A (enrdf_load_stackoverflow) | 1970-05-14 |
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