US3649279A - Photographic compositions with a thiosemicarbazone solubilizing agent - Google Patents
Photographic compositions with a thiosemicarbazone solubilizing agent Download PDFInfo
- Publication number
- US3649279A US3649279A US3174A US3649279DA US3649279A US 3649279 A US3649279 A US 3649279A US 3174 A US3174 A US 3174A US 3649279D A US3649279D A US 3649279DA US 3649279 A US3649279 A US 3649279A
- Authority
- US
- United States
- Prior art keywords
- silver halide
- formula
- photographic
- radicals
- thiosemicarbazone
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 90
- 239000002904 solvent Substances 0.000 title claims abstract description 78
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical compound CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 title claims description 22
- 229910052709 silver Inorganic materials 0.000 claims abstract description 171
- 239000004332 silver Substances 0.000 claims abstract description 171
- -1 silver halide Chemical class 0.000 claims abstract description 150
- 125000001424 substituent group Chemical group 0.000 claims abstract description 40
- 238000000034 method Methods 0.000 claims abstract description 29
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 13
- 125000003118 aryl group Chemical group 0.000 claims abstract description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 12
- 150000001299 aldehydes Chemical class 0.000 claims abstract description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 11
- 239000001257 hydrogen Substances 0.000 claims abstract description 11
- 238000012545 processing Methods 0.000 claims description 57
- 239000000839 emulsion Substances 0.000 claims description 44
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 40
- 239000003795 chemical substances by application Substances 0.000 claims description 30
- 238000012546 transfer Methods 0.000 claims description 22
- 239000000126 substance Substances 0.000 claims description 10
- 230000003381 solubilizing effect Effects 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- JOOXCMJARBKPKM-UHFFFAOYSA-N 4-oxopentanoic acid Chemical compound CC(=O)CCC(O)=O JOOXCMJARBKPKM-UHFFFAOYSA-N 0.000 claims description 8
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 claims description 8
- WOOLWGHQYCIONW-VAYJURFESA-N [[(2S,3R,4S)-2,3,4,5-tetrahydroxypentylidene]amino]thiourea Chemical group C([C@H](O)[C@@H](O)[C@@H](O)CO)=NNC(N)=S WOOLWGHQYCIONW-VAYJURFESA-N 0.000 claims description 5
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 claims description 5
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 4
- 229940040102 levulinic acid Drugs 0.000 claims description 4
- 239000001294 propane Substances 0.000 claims description 4
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical group O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 claims description 4
- OMQATPITDSAIFV-IEEROJAVSA-N [(e)-[(2s,3r,4r,5r)-2,3,4,5,6-pentahydroxyhexylidene]amino]thiourea Chemical compound NC(=S)N\N=C\[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO OMQATPITDSAIFV-IEEROJAVSA-N 0.000 claims description 3
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 claims description 3
- FAHQMNLLWZQONW-UHFFFAOYSA-N (1,1-dihydroxypropan-2-ylideneamino)thiourea Chemical compound OC(C(C)=NNC(N)=S)O FAHQMNLLWZQONW-UHFFFAOYSA-N 0.000 claims description 2
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 claims description 2
- BJLGMFGFJVYGIN-UHFFFAOYSA-N 2-[(carbamothioylhydrazinylidene)methyl]benzoic acid Chemical compound NC(=S)NN=CC1=CC=CC=C1C(O)=O BJLGMFGFJVYGIN-UHFFFAOYSA-N 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 2
- 239000000463 material Substances 0.000 description 23
- 150000003254 radicals Chemical class 0.000 description 17
- 239000000243 solution Substances 0.000 description 15
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 8
- 229920002301 cellulose acetate Polymers 0.000 description 8
- 238000009792 diffusion process Methods 0.000 description 6
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 6
- 108010010803 Gelatin Proteins 0.000 description 5
- 230000002378 acidificating effect Effects 0.000 description 5
- 229920003086 cellulose ether Polymers 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 229920000159 gelatin Polymers 0.000 description 5
- 239000008273 gelatin Substances 0.000 description 5
- 235000019322 gelatine Nutrition 0.000 description 5
- 235000011852 gelatine desserts Nutrition 0.000 description 5
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 5
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 4
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 229940042396 direct acting antivirals thiosemicarbazones Drugs 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 4
- 230000001376 precipitating effect Effects 0.000 description 4
- 150000003584 thiosemicarbazones Chemical class 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000005083 Zinc sulfide Substances 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000000084 colloidal system Substances 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 239000002667 nucleating agent Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 150000004763 sulfides Chemical class 0.000 description 3
- 229910052984 zinc sulfide Inorganic materials 0.000 description 3
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 3
- WQZGKKKJIJFFOK-SVZMEOIVSA-N (+)-Galactose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-SVZMEOIVSA-N 0.000 description 2
- ZVNPWFOVUDMGRP-UHFFFAOYSA-N 4-methylaminophenol sulfate Chemical compound OS(O)(=O)=O.CNC1=CC=C(O)C=C1.CNC1=CC=C(O)C=C1 ZVNPWFOVUDMGRP-UHFFFAOYSA-N 0.000 description 2
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- SRBFZHDQGSBBOR-HWQSCIPKSA-N L-arabinopyranose Chemical compound O[C@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-HWQSCIPKSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 229930182830 galactose Natural products 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- BRWIZMBXBAOCCF-UHFFFAOYSA-N hydrazinecarbothioamide Chemical compound NNC(N)=S BRWIZMBXBAOCCF-UHFFFAOYSA-N 0.000 description 2
- 230000002452 interceptive effect Effects 0.000 description 2
- 239000011133 lead Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 150000007659 semicarbazones Chemical class 0.000 description 2
- 238000000926 separation method Methods 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
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- VKGQPUZNCZPZKI-UHFFFAOYSA-N (diaminomethylideneamino)azanium;sulfate Chemical compound NN=C(N)N.NN=C(N)N.OS(O)(=O)=O VKGQPUZNCZPZKI-UHFFFAOYSA-N 0.000 description 1
- YBDSNEVSFQMCTL-UHFFFAOYSA-N 2-(diethylamino)ethanethiol Chemical compound CCN(CC)CCS YBDSNEVSFQMCTL-UHFFFAOYSA-N 0.000 description 1
- ZQLIJRZJTLXEMQ-UHFFFAOYSA-N 3,4-diaminophenol;hydrochloride Chemical compound Cl.NC1=CC=C(O)C=C1N ZQLIJRZJTLXEMQ-UHFFFAOYSA-N 0.000 description 1
- VPIXQGUBUKFLRF-UHFFFAOYSA-N 3-(2-chloro-5,6-dihydrobenzo[b][1]benzazepin-11-yl)-N-methyl-1-propanamine Chemical compound C1CC2=CC=C(Cl)C=C2N(CCCNC)C2=CC=CC=C21 VPIXQGUBUKFLRF-UHFFFAOYSA-N 0.000 description 1
- FJWJYHHBUMICTP-UHFFFAOYSA-N 4,4-dimethylpyrazolidin-3-one Chemical compound CC1(C)CNNC1=O FJWJYHHBUMICTP-UHFFFAOYSA-N 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- MNQZXJOMYWMBOU-VKHMYHEASA-N D-glyceraldehyde Chemical compound OC[C@@H](O)C=O MNQZXJOMYWMBOU-VKHMYHEASA-N 0.000 description 1
- SHZGCJCMOBCMKK-UHFFFAOYSA-N D-mannomethylose Natural products CC1OC(O)C(O)C(O)C1O SHZGCJCMOBCMKK-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- PNNNRSAQSRJVSB-UHFFFAOYSA-N L-rhamnose Natural products CC(O)C(O)C(O)C(O)C=O PNNNRSAQSRJVSB-UHFFFAOYSA-N 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- BZKLDUBXTMDNMW-FACPPWRESA-N [(e)-[(2e)-2-(carbamothioylhydrazinylidene)ethylidene]amino]thiourea Chemical compound NC(=S)N\N=C\C=N\NC(N)=S BZKLDUBXTMDNMW-FACPPWRESA-N 0.000 description 1
- UYHCMAZIKNVDSX-POHAHGRESA-N [(z)-benzylideneamino]thiourea Chemical compound NC(=S)N\N=C/C1=CC=CC=C1 UYHCMAZIKNVDSX-POHAHGRESA-N 0.000 description 1
- OMQATPITDSAIFV-SLPGGIOYSA-N [[(2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexylidene]amino]thiourea Chemical compound NC(=S)NN=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO OMQATPITDSAIFV-SLPGGIOYSA-N 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- FQUDPIIGGVBZEQ-UHFFFAOYSA-N acetone thiosemicarbazone Chemical compound CC(C)=NNC(N)=S FQUDPIIGGVBZEQ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- PNNNRSAQSRJVSB-BXKVDMCESA-N aldehydo-L-rhamnose Chemical compound C[C@H](O)[C@H](O)[C@@H](O)[C@@H](O)C=O PNNNRSAQSRJVSB-BXKVDMCESA-N 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- XIWMTQIUUWJNRP-UHFFFAOYSA-N amidol Chemical compound NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines 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
- 238000004458 analytical method Methods 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- JIRRNZWTWJGJCT-UHFFFAOYSA-N carbamothioylthiourea Chemical compound NC(=S)NC(N)=S JIRRNZWTWJGJCT-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- AJPXTSMULZANCB-UHFFFAOYSA-N chlorohydroquinone Chemical compound OC1=CC=C(O)C(Cl)=C1 AJPXTSMULZANCB-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- KYRUBSWVBPYWEF-UHFFFAOYSA-N copper;iron;sulfane;tin Chemical compound S.S.S.S.[Fe].[Cu].[Cu].[Sn] KYRUBSWVBPYWEF-UHFFFAOYSA-N 0.000 description 1
- KTTMEOWBIWLMSE-UHFFFAOYSA-N diarsenic trioxide Chemical compound O1[As](O2)O[As]3O[As]1O[As]2O3 KTTMEOWBIWLMSE-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- OAEGRYMCJYIXQT-UHFFFAOYSA-N dithiooxamide Chemical compound NC(=S)C(N)=S OAEGRYMCJYIXQT-UHFFFAOYSA-N 0.000 description 1
- 125000001242 enediol group Chemical group 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- MNQZXJOMYWMBOU-UHFFFAOYSA-N glyceraldehyde Chemical compound OCC(O)C=O MNQZXJOMYWMBOU-UHFFFAOYSA-N 0.000 description 1
- FDWREHZXQUYJFJ-UHFFFAOYSA-M gold monochloride Chemical compound [Cl-].[Au+] FDWREHZXQUYJFJ-UHFFFAOYSA-M 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 125000000687 hydroquinonyl group Chemical group C1(O)=C(C=C(O)C=C1)* 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- CBEQRNSPHCCXSH-UHFFFAOYSA-N iodine monobromide Chemical compound IBr CBEQRNSPHCCXSH-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- TYQCGQRIZGCHNB-JLAZNSOCSA-N l-ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(O)=C(O)C1=O TYQCGQRIZGCHNB-JLAZNSOCSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- PJUIMOJAAPLTRJ-UHFFFAOYSA-N monothioglycerol Chemical compound OCC(O)CS PJUIMOJAAPLTRJ-UHFFFAOYSA-N 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- BTFQKIATRPGRBS-UHFFFAOYSA-N o-tolualdehyde Chemical compound CC1=CC=CC=C1C=O BTFQKIATRPGRBS-UHFFFAOYSA-N 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 150000004989 p-phenylenediamines Chemical class 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- ZWLUXSQADUDCSB-UHFFFAOYSA-N phthalaldehyde Chemical compound O=CC1=CC=CC=C1C=O ZWLUXSQADUDCSB-UHFFFAOYSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003346 selenoethers Chemical class 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
- 229940001593 sodium carbonate Drugs 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- PPASLZSBLFJQEF-RKJRWTFHSA-M sodium erythorbate Chemical compound [Na+].OC[C@@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RKJRWTFHSA-M 0.000 description 1
- 235000010352 sodium erythorbate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- RBWFXUOHBJGAMO-UHFFFAOYSA-N sulfanylidenebismuth Chemical class [Bi]=S RBWFXUOHBJGAMO-UHFFFAOYSA-N 0.000 description 1
- WWNBZGLDODTKEM-UHFFFAOYSA-N sulfanylidenenickel Chemical compound [Ni]=S WWNBZGLDODTKEM-UHFFFAOYSA-N 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- YUKQRDCYNOVPGJ-UHFFFAOYSA-N thioacetamide Chemical compound CC(N)=S YUKQRDCYNOVPGJ-UHFFFAOYSA-N 0.000 description 1
- DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- 229940035024 thioglycerol Drugs 0.000 description 1
- CWERGRDVMFNCDR-UHFFFAOYSA-M thioglycolate(1-) Chemical compound [O-]C(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-M 0.000 description 1
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
- 229910001432 tin ion Inorganic materials 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
- C07H5/04—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium to nitrogen
- C07H5/06—Aminosugars
-
- 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
-
- 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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/32—Development processes or agents therefor
- G03C8/36—Developers
- G03C8/365—Developers containing silver-halide solvents
Definitions
- VISCOUS PROCESSING COMPOSITION SILVER HALIDE EMULSION SUPPORT 22 I SILVER HALIDE EMULSION LAYER 2 2
- the present invention relates to novel silver halide solubilizing agents and photographic compositions containing said agent.
- Silver halide solubilizing materials are also utilized in chemical transfer processes wherein unexposed and undeveloped silver halide is transferred to a receiving sheet or a web, the solubilizing agent facilitating the transfer of such silver halide.
- Silver halide solubilizing agents also have utility in so-called monobaths wherein a single processing solution can be utilized to both develop and fix a photographic silver halide emulsion layer.
- silver halide solubilizing agents are known in the art.
- One example is the thiosugar silver halide solubilizing agents ha in g t he g eneral formula:
- the silver halide solubilizing agents of the present invention are not to be confused with the antifading materials noted in US. Pat. 3,239,340 issued Mar. 8, 1966, (see column 3).
- Those antifading materials including acetonethiosemicarbazone and benzaldehydethiosemicarbazone are used to prevent fading of an image under high humidity conditions and then only in combination with conventional fixing agents such as the alkali thiosulfates, alkali thiocyanates, ammonium thiosulfate and ammonium thiocyanate.
- R is a substituent selected from the group consisting of hydrogen, substituted and unsubstituted alkyl, aryl and heterocyclic radicals, and radicals derived from polyhydroxy aldehydes, said radicals having the formula:
- R is a substituent selected from the group consisting of R and radicals having the formula:
- a photographic chemical transfer method for processing an image-exposed silver halide emulsion layer which comprises developing said silver halide to produce a negative silver image, treating the resulting developed silver halide emulsion layer with an aqueous composition, transferring unexposed and undeveloped silver halide to a reception layer containing a silver halide precipitant, and reducing the said transferred silver halide to silver, said aqueous composition containing at least about 3 grams per liter of said composition of a silver halide solubilizing agent having the formula shown above.
- a process for solubilizing unexposed and undeveloped silver halide on a photographic element which comprises treating said silver halide with an aqueous composition comprising at least about 3 grams per liter of said composition of a silver halide solubilizing agent having the formula shown above.
- an aqueous composition containing a silver halide developing agent and at least about 3 grams per liter of said composition of a silver halide solubilizing agent having the formula shown above.
- an aqueous photographic monobath composition being suitable for both developing and fixing photographic silver halide emulsions and comprising a photographic silver halide developing agent and at least about 3 grams per liter of said composition of a silver halide solubilizing agent having the formula shown above.
- an aqueous viscous photographic monobath composition being suitable for both developing and fixing photographic silver halide emulsions comprising a photographic silver halide developing agent, a viscosity-increasing material and at least about 3 grams per liter of said composition of a silver halide solubilizing agent having the formula shown above.
- the alkyl radicals from which the R substituent may be selected generally have one to carbon atoms and can include such non-interfering substituents as alkyl, aryl, sulfonyl, carboxyl, amino, and the like.
- the aryl radicals from which the R substituents may be selected are of the phenyl or naphthyl series and can include various non-interfering substituents such as alkyl, sulfonyl, carboxyl, amino, and the like.
- Various heterocyclic radicals contemplated within the scope of this invention are preferably rings having five to six atoms such as morpholino, oxapentamethylene, pyridyl, thiazolyl, and the like.
- hydroxyl radical is preferred as it generally tends to enhance the water solubility of the solubilizing agents.
- a particularly useful class of solubilizing agents according to the present invention are water soluble compounds prepared by reacting polyhydroxy aldehydes such as mannose, glucose, galactose, glyceraldehyde and the like with thiosemicarbazide, and which can be represented by the formula:
- x is an integer of l to 4 and R is hydrogen and R is as defined hereinabove.
- said solubilizing agents generally comprise a particular class of thiosemicarbazones and thiocarbohydrazones. Synthesis of these thiosemicarbazones and thiocarbohydrazones can be prepared by reaction techniques and methods well known to those skilled in the art.
- the thiosemicarbazone solubilizing agents of the present invention can be prepared by reacting a thiosemicarbazide with an aldehyde or a ketone in accordance with usual practice.
- Typical suitable solubilizing agents that can be utilized in the present invention include:
- D,L-glyceraldehyde thiosemicarbazone D-m annose thiosemicarbazone D galactose thiosemicarbazone morpholino-Z-propanone thiosemicarbazone o-phthaldehyde monoacid thiosemicarbazone glyoxal bis(thiosemicarbazone) benzaldehyde (4-phenyl-3-thio)-semicarbazone o-tolylaldehyde thiosemicarbazone D-xylose thiosemicarbazone L-arabinose thiosemicarbazone propionaldehyde thiosemicarbazone p-dimethylaminobenzaldehyde thiosemicarbazone B-morpholinoethylthio-Z-propanone thiosemicarbazone diethylamino-2-propanone thiosemicarbazone pyridy
- carbohydrazones which can be used include:
- D-galactose thiocarbohydrazone D-mannose thiocarbohydrazone L-rhamnose thiocarbohydrazone Double-ended thiocarbohydrazones which may be used include:
- the subject silver halide solubilizing agents are typically utilized in aqueous compositions containing at least about 3 grams of solubilizing agent per liter of composition.
- the amount of such silver halide solubilizing agent utilized can be widely varied, the amount used being readily ascertainable by one skilled in the art for the particular photographic application. Generally, however, the amount of solubilizing agent utilized would vary between about 3 grams and 200 grams per liter of processing composition.
- the subject solubilizing agents are utilized in baths for clearing or fixing developed photographic film, at least 5 or 10 to 200 grams of solubilizing agent per liter of processing solution are more generally utilized to obtain fixing within a practical time interval. Lower concentrations, down to about 3 grams of the subject solubilizing agent per liter, are more generally utilized as the silver halide solvent in chemical transfer processing.
- solubilizing agent of the present invention exhibit fixing or clearing activity in acidic and neutral aqueous media as well as alkaline solution.
- the subject solubilizing agents may be utilized in aqueous solutions having a pH less than about 12.0.
- the pH of I processing compositions may be varied to a pH higher than about 12.0, it is generally not preferred to do so because the very high pH of such aqueous compositions may tend to fog the silver halide emulsion.
- Various acidic materials and alkaline materials may be utilized to acquire the desired acidity or alkalinity. Acidic materials such as acetic acid, hydrochloric acid, and the like may be used to achieve the desired acidity.
- Alkali metal carbonates and hydroxides and amines can be utilized to acquire the desired alkalinity.
- Monobaths which can be utilized to both develop and fix an exposed photographic silver halide emulsion are well known in the art.
- Such monobaths contain both a photographic developing agent suitable for developing or reducing latent silver halide images to silver and a silver halide solubilizing or fixing agent such as ammonium thiocyanate, sodium thiosulfate, and the like.
- the subject solubilizing agents can be utilized in lieu of the conventional sodium thiosulfate and the like silver halide solubilizing agents in such monobath compositions.
- Typical silver halide developing agents that can be employed in monobath compositions include such hydroquinonyl compounds as hydroquinone, N-methyl-p-aminophenolsulfate, chlorohydroquinone, 2,4-diaminophenol and 3,4- diaminophenol hydrochloride; 3-pyrazolidones such as lphenyl-3-pyrazolidone, 4-m ethyll-phenyl-3 -py razolidone and l-phenyl-4,4-dimethyl-3-pyrazolidone; ene-dioles such as ascorbic acid; catechol; pyrogallol; gallic acid; p-phenylene diamines; and the like, as well as mixtures of such developing agents.
- hydroquinonyl compounds as hydroquinone, N-methyl-p-aminophenolsulfate, chlorohydroquinone, 2,4-diaminophenol and 3,4- diaminophenol hydrochloride; 3-
- Monobaths of the invention that have high viscosity are particularly useful processing compositions.
- High viscosity monobath compositions are desirable as they can be readily spread in a uniform layer on the film to be processed.
- Such compositions desirably have viscosities in excess of about 500 centipoises at a temperature of approximately 24 C. and preferably of the order of 1,000 to 20,000 centipoises at this temperature.
- a wide variety of thickening agents can be added to monobath compositions to impart high viscosities.
- Such viscosity-imparting materials are film-forming materials that retain this property and their viscosity in aqueous solution. Suitable viscositydncreasing materials include sodium carboxymethylcellulose, hydroxyethylcellulose, polyvinyl alcohol, sodium salts of polymethacrylic acid and polyacrylic acid, and the like.
- the subject thiosugars have particular utility as silver halide solvents in photographic chemical transfer processes.
- Such transfer processes are well known in the art.
- Rott in US. Pat. No. 2,352,014 described such a transfer process for preparing reversal images.
- an exposed photographic silver halide emulsion is impregnated with a developer and pressed in contact with a receiving sheet in the presence of a silver halide solvent and a fogging agent.
- the undeveloped silver halide in the emulsion layer is transferred by means of the silver halide solvent to the receiving sheet, this transferred silver halide developing to silver to form a positive image on the receiving sheet.
- Land suggested the use of various specific fogging agents or nuclei that could be used in the reception layer to facilitate the formation of a silver image therein and the use of viscous processing materials to facilitate the utilization of processing materials in pods positioned between the light-sensitive negative layer and the reception layer.
- Land patents as US. Pat. Nos. 2,543,181, 2,584,029 and 2,698,236 for suitable photographic silver halide transfer processes in which the present silver halide solvents can be effectively utilized.
- nuclei or silver halide precipitating agents can be utilized in the reception layers used in silver halide solvent transfer processes.
- Such nuclei are incorporated into conventional photographic organic hydrophilic colloid layers and include such physical nuclei or chemical precipitants as:
- salts the anions of which form silver salts less soluble than the silver halide of the photographic emulsion to be processed
- nondiffusing polymeric materials with functional groups capable of combining with and in solubilizing silver ions.
- Typical useful silver precipitating agents include sulfides, selenides, polysulfides, polyselenides, thiourea and its derivatives, mercaptans, stannous halides, silver, gold, platinum, palladium, mercury, colloidal silver, aminoguanidine sulfate, aminoguanidine carbonate, arsenous oxide, sodium stannite, substituted hydrazines, zanthates, and the like.
- Polyvinyl mercaptoacetate is an example of a suitable nondiffusing polymeric silver precipitant.
- Heavy metal sulfides such as lead, silver, zinc, aluminum, cadmium and bismuth sulfides are useful, particularly the sulfides of lead and zinc alone or in an admixture, or complex salts of these with thioacetamide, dithio-oxamide or dithio-biuret.
- the heavy metals and the novel metals particularly in colloidal form are especially effective.
- Other silver precipitating agents will occur to those skilled in the present art.
- Such silver precipitating or nucleating agents can be utilized in reception layers that are separate elements from the lightsensitive silver halide negative element being processed, or they can be utilized as reception layers integral with the lightsensitive negative element.
- the reception layer is typically in the form ofa web imbibed with processing material of the type suitable for processing long units of film such as motion picture film, or in the form of a support for receiving positive images of the snapshot type that are processed in accordance with the Land patents referred to above.
- Belgian Pat. No. 472,243 and Tregillus et al. US. Pat. Ser. No. 835,473 filed Aug. 24, 1959 describe typical solvent transfer processes utilizing webs as a silver halide reception means.
- reception layer When the reception layer is integral with the light-sensitive negative element, such reception layer is generally a sublayer over which is coated the silver halide in a vehicle that is readily removable during processing such as a hydrophilic colloid soluble in aqueous alkali like cellulose ether phthalate.
- FIGS. 1 to 4 illustrate fragmentary views in sectional elevation of typical light-sensitive elements that can be processed in accordance with the invention as well as typical processing methods of the invention utilizing the present silver halide solubilizing agents.
- FIG. 1 illustrates a typical light-sensitive element comprising support 10 having coated thereon silver halide emulsion layer 11.
- the above-described monobath compositions containing both a developing agent and a solubilizing agent of the invention thickened to a high viscosity with a thickening material can be spread on the surface of layer 11 as illustrated by viscous composition 12 in the drawings.
- the viscous processing composition thereafter is typically removed from the silver halide emulsion layer by wiping, squeegeeing or by washing.
- FIG. 2 of the drawings illustrates a typical light-sensitive element having an integral nucleated reception layer that can be utilized to prepare positive images without the necessity of a separate image receiving sheet.
- nucleated reception layer 21 which is typically an organic hydrophilic colloid material such as hardened gelatin containing any of the nucleating agents described above.
- silver halide emulsion layer 22 comprising silver halide dispersed in a substrate that can be readily removed during or after processing. In the processing of a light-sensitive element of the type illustrated in FIG. 2, a latent image is formed in silver halide emulsion layer 22 on exposure.
- the resulting exposed element can thereafter be treated with a monobath composition of the type described above either by immersing the element in a solution of the monobath or by coating the surface of the element with a viscous monobath processing composition, such monobaths containing the present silver halide solubilizing agents.
- a silver negative image is developed in silver halide emulsion layer 22 and unexposed and undeveloped silver halide in this emulsion layer is transferred to nucleated reception layer 21.
- the transferred silver halide develops to form a positive silver image.
- Silver halide emulsion layer 22 containing the negative silver image is removed either during the course of the processing by the aqueous processing composition or by subsequently washing off.
- FIG. 3 of the drawing illustrates a typical light-sensitive negative element and a sheet for receiving images transferred from the negative element. Also included in FIG. 3 is a pod containing a viscous processing composition positioned between the light-sensitive negative element and the receiving sheet.
- a viscous processing composition positioned between the light-sensitive negative element and the receiving sheet.
- silver halide emulsion layer 31 which serves as the light-sensitive negative element or film material.
- the receiving sheet comprises support 35 having coated thereon nucleated reception layer 34. Typical nucleating agents are described in detail hereinabove.
- pod 31 containing viscous processing composition 32 Positioned between the receiving sheet and the light-sensitive negative element is pod 31 containing viscous processing composition 32. Viscous processing composition 32 can be any of the viscous monobaths described above.
- a latent image is formed in layer 31.
- Processing of this light-sensitive element is effected by drawing the sandwiched layers illustrated in FIG. 3 through rollers to rupture pod 33 and spread a uniform layer of viscous processing composition 32 between silver halide emulsion layer 31 and nucleated reception layer 34.
- the latent negative image is developed to silver in layer 31 and remaining unexposed and undeveloped silver halide in layer 31 is transferred to nucleated reception layer 34 wherein it is developed to form a positive silver image.
- nucleated reception layer 34 On separation of the receiving sheet from the light-sensitive negative element, a positive silver image remains on the receiving sheet.
- Such a chemical transfer process has particular utility for rapid incamera processing applications.
- FIG. 4 of the drawings illustrates a typical processing web spooled or sandwiched with a photographic film to be processed.
- the processing web comprises web support 40 having coating thereon nucleated reception layer 41.
- nucleated reception layer comprises an organic hydrophilic substrate having therein development nuclei of the type described above.
- the photographic film to be processed comprises support 43 having coated thereon silver halide emulsion layer 44.
- the web and the photographic film are sandwiched together so that nucleated reception layer 41 of the web is in intimate contact with silver halide emulsion layer 44 of the film on spool 42.
- a diffusion transfer processing composition including a solubilizing agent of the invention as a silver halide solvent is imbibed onto the web.
- the web and the film are left in the sandwiched or wound form on spool 42 until the processing of the silver halide emulsion layer is complete.
- a negative silver image is formed in silver halide emulsion layer 44 corresponding to regions of exposure, and unexposed and undeveloped silver halide in this layer is transferred to nucleated reception layer 42 and developed to silver.
- Such web processing techniques have particular utility for processing strips of film such as microfilm and motion picture film up to 100 feet or more in length.
- the subject silver halide solubilizing agents have many superior properties over currently used agents for this purpose.
- the subject agents do not have the strong characteristic odors which characterize many of the conventional sulfur-containing fixing agents, such as thioglycerol, mercaptoacetic acid, diethylaminoethanethiol and others.
- the present fixing agents produce silver images having colder image tones than conventional fixing agents. Further, emulsions fixed with the present thiosugars exhibit improved detail in shadow areas and desirable light edge effects.
- EXAMPLE 1 Each of the following thiosemicarbazones are dissolved in the media noted in Table 1 below.
- a strip of Fine Grain Positive Film (a bromoiodide film of 350 mg. Ag/ft?) is attached to the arm ofa mechanical agitator which completes 2 up-anddown cycles per second, each of the four strokes being onehalf inch in length.
- the fixing activity of these various thiosemicarbazone solubilizing agents is measured as the time it takes the film to clear. Clearing time is measured visually and this time is recorded in Table 1 shown below.
- the above formulation is heated to 120 F. to dissolve the above materials.
- the pH of the above formulation is about 10.0.
- a photographic film of the type described in Example 1 above is exposed to a photographic step tablet and processed for 3 minutes at 75 F. in the above illustrated monobath formulation.
- a black silver image is formed and the silver halide is fixed from the unexposed areas.
- the developed silver image has a minimum density of0.04, a maximum density of 1.32, and a gamma of 1.58.
- the above diffusion transfer solution exhibits a pH of about 10.3.
- a strip of a photographic film as described in Example 1 above is exposed, then immersed in the above shown diffusion transfer solution for 30 seconds at 75 F.
- the film emulsion is then pressed in contact with a nucleated receiver containing zinc sulfide nuclei in a gelatin matrix for 60 seconds before stripping apart. The result is only a very faint, light tan positive image.
- EXAMPLE 4 A viscous diffusion transfer solution may be made by adding a viscosity imparting material to the solution described above in Example 3. This may be accomplished by making a l-liter aqueous solution containing the same components listed in Example 3 above and in addition adding grams of L- arabinose thiosemicarbazone solubilizing agent and 10 grams of hydroxyethylcellulose as a viscosity imparting material.
- the viscosity of the resulting l-liter composition is about 25 c.p.s.
- Pods may be prepared for the above processing composition from aluminum foil lined with polyethylene. Ten-milliliter portions of the processing composition may then be heat sealed into the pods.
- a negative film comprising a high-speed, coarse-grain, negative-type, developing-out gelatino-silver bromoiodide emulsion on a cellulose acetate film support and a receiving sheet comprising a white-colored cellulose acetate film support having coated thereon a gelatin layer containing nickel sulfide nuclei are then readied for use. Processing may be carried out by positioning a pod containing the processing composition between the receiving sheet and the negative film as illustrated in FIG. 3 of the drawings.
- the resulting sandwich may then be pulled between rollers to rupture the pod and spread a uniform layer of processing solution between the negative film and the receiving sheet.
- the layers of the sandwich may be left in contact for about 2 minutes at about 75 F.
- a positive silver image is present on the receiving sheet.
- the silver halide solubilizing agents of the invention may also be used in producing direct-positive images without the aid of a separate receiving sheet or element.
- a light-sensitive photographic film of the type illustrated by FIG. 2 in the drawings is prepared by coating on a transparent cellulose acetate base a sublayer of hardened gelation containing zinc sulfide nuclei. Over the resulting layer is coated a high-speed, coarse-grain, negative-type, developing-out emulsion of silver bromoiodide in a soluble cellulose ether phthalate substrate. The resulting film is exposed in an intensity scale sensitometer and thereafter processed for about 4 minutes at 75 F. in the following processing composition:
- sodium sulfite desiccated 75 g potassium bromide 1.0 g 4-methyl-l-phenyl-3-pyrazolidone 1.0 g sodium isoascorbate 3.0 g hydroquinone 8.0 g L-arabinose lhiosemicarbazone 15.0 g sodium carbonate 30.0 g. water to make 1 1.
- a negative silver image is developed in the silver halide cellulose ether phthalate layer.
- Unexposed and undeveloped silver halide in this layer is dissolved by the solubilizing agent in the processing composition and is transferred to the hardened gelatin zinc sulfide nuclei-containing underlayer wherein the silver halide is developed or is reduced to silver to form a positive silver image.
- the cellulose ether phthalate is soluble in aqueous media, the cellulose ether phthalate containing the negative silver layer is readily washed away leaving a positive silver image.
- EXAMPLE 6 The subject thiosugars can also be utilized in viscous monobath processing compositions as silver halide solvents in processes not utilizing silver halide reception elements.
- the following processing composition was prepared:
- methylaminoethanol-sulfur dioxide-addition product (17.8% 50,) 75.0 g. 4.4-dimethyll -phenyl-3- pyrazolidone 2.0 g. hydroquinone 10.0 g L-arabinose thiosemicarbazone 45.0 g. potassium iodide 0.5 g pH 10.5 water to make 10 l. colloidal silver (Carey Lea Silver) 0.2 g natrosol (hydroxyethylcellulose) 0.2 g
- the prepared viscous processing composition is used to process a light-sensitive film comprising a high-speed, coarsegrain, negative-type, developing-out, gelatino-silver bromoiodide emulsion on a cellulose acetate film base.
- the film is exposed in an intensity scale sensitometer and a layer of the viscous processing composition is spread over the emulsion surface of the film as illustrated in FIG. 1 in the drawings.
- the processing composition is squeegeed from the film.
- a fully processed film having a lightand heat-stable negative silver image results.
- Unexposed silver halide is removed during the processing.
- the viscosity of the above solution may be varied by the addition of higher amounts of thickening agents. Useful viscosity ranges cover between 1,000 to 200,000 centipoises.
- EXAMPLE 7 The subject thiosugar silver halide solubilizing agents can be utilized in monobaths which are imbibed on processing webs used to develop and fix silver halide emulsion layers.
- a typical suitable processing composition has the following formulatron:
- a process web is prepared by coating on a cellulose acetate support a layer comprising 2 g. of gelatin and 8 mg. of Carey Lea silver per square foot. This web is soaked for about 5 minutes in the monobath processing composition described above at F. prior to winding or coiling in contact with the film to be processed in the manner illustrated in FIG. 4 of the drawings.
- a high-speed, coarse-grain, negative-type, developing-out, gelatino-silver bromoiodide emulsion coated on a cellulose acetate film support that has been exposed is processed by bringing the silver halide emulsion layer of the film in intimate contact with the nucleated layer of the soaked web and by allowing the resulting rolled sandwich to be maintained for 10 minutes at 75 F.
- An aqueous composition consisting essentially of a silver halide developing agent and at least about 3 grams per liter of said composition of a silver halide solubilizing agent having the formula:
- R is a substituent selected from the group consisting of hydrogen, substituted and unsubstituted alkyl, aryl and heterocyclic radicals, and radicals derived from polyhydroxy aldehydes, said radicals having the formula:
- x is an integer l to 4; wherein R is a substituent selected from the group consisting of R and radicals having the formula:
- An photographic monobath composition being suitable for both developing and fixing photographic silver halide emulsions comprising a photographic silver halide developing agent and at least about 3 grams per liter of said composition of a silver halide solubilizing agent having the formula:
- R R- 3 N-NH-i -Nn-R'
- R is a substituent selected from the group consisting of hydrogen, substituted and unsubstituted alkyl, aryl and heterocyclic radicals, and radicals derived from polyhydroxy aldehydes, said radicals having the formula:
- a photographic monobath composition as described in claim 3 wherein at least one of the R substituents of the solubilizing agent has the formula:
- x is an integer l to 4.
- a photographic monobath composition according to claim 7 which has a viscosity of about 1,000 to 200,000 centipoises at 24 C. and wherein the developing agent is a 3- pyrazolidone.
- a photographic chemical transfer method for processing an image-exposed silver halide emulsion layer which comprises developing said silver halide to produce a negative silver image, treating the resulting developed silver halide emulsion layer with an aqueous composition, transferring unexposed and undeveloped silver halide to a reception layer containing a silver halide precipitant, and reducing the said transferred silver halide to silver, said aqueous composition containing at least about 3 grams per liter of said composition of a silver halide solubilizing agent having the formula:
- R is a substituent selected from the group consisting of hydrogen, substituted and unsubstituted alkyl, aryl and heterocyclic radicals, and radicals derived from polyhydroxy aldehydes, said radicals having the formula:
- R is a substituent selected from the group consisting of hydrogen, substituted and unsubstituted alkyl, aryl and heterocyclic radicals, and radicals derived from polyhydroxy aldehydes, said radicals having the formula:
- silver halide solubilizing agent is a member selected from the group consisting of:
- a process according to claim 11 wherein at least one of the R substituents of the silver halide solubilizing agent has the structural formula:
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---|---|---|---|---|
ZA81418B (en) * | 1980-02-06 | 1982-08-25 | Gulf Oil Corp | Substituted thiosemicarbazones and use as plant growth regulants |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2543181A (en) * | 1947-01-15 | 1951-02-27 | Polaroid Corp | Photographic product comprising a rupturable container carrying a photographic processing liquid |
US3326689A (en) * | 1964-01-20 | 1967-06-20 | Eastman Kodak Co | Photographic direct-print silver halide emulsions |
-
1970
- 1970-01-15 US US3174A patent/US3649279A/en not_active Expired - Lifetime
- 1970-12-04 CA CA099839A patent/CA928127A/en not_active Expired
-
1971
- 1971-01-13 FR FR7100882A patent/FR2090478A5/fr not_active Expired
- 1971-01-14 BE BE761593A patent/BE761593A/xx unknown
- 1971-01-14 GB GB183371A patent/GB1333292A/en not_active Expired
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2543181A (en) * | 1947-01-15 | 1951-02-27 | Polaroid Corp | Photographic product comprising a rupturable container carrying a photographic processing liquid |
US3326689A (en) * | 1964-01-20 | 1967-06-20 | Eastman Kodak Co | Photographic direct-print silver halide emulsions |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011022347A1 (en) | 2009-08-18 | 2011-02-24 | The Lubrizol Corporation | Antiwear composition and method of lubricating an internal combustion engine |
Also Published As
Publication number | Publication date |
---|---|
FR2090478A5 (enrdf_load_stackoverflow) | 1972-01-14 |
CA928127A (en) | 1973-06-12 |
BE761593A (fr) | 1971-06-16 |
GB1333292A (en) | 1973-10-10 |
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