US3733199A - Photographic composition of sodium and potassium ions for treating direct positive emulsions - Google Patents
Photographic composition of sodium and potassium ions for treating direct positive emulsions Download PDFInfo
- Publication number
- US3733199A US3733199A US00152978A US3733199DA US3733199A US 3733199 A US3733199 A US 3733199A US 00152978 A US00152978 A US 00152978A US 3733199D A US3733199D A US 3733199DA US 3733199 A US3733199 A US 3733199A
- Authority
- US
- United States
- Prior art keywords
- sodium
- silver halide
- potassium
- silver
- composition
- 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 abstract description 39
- 239000000839 emulsion Substances 0.000 title abstract description 33
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group 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 title abstract description 19
- 239000011734 sodium Substances 0.000 title abstract description 19
- 229910001414 potassium ion Inorganic materials 0.000 title description 3
- 229910001415 sodium ion Inorganic materials 0.000 title description 2
- -1 SILVER HALIDE Chemical class 0.000 abstract description 57
- 229910052709 silver Inorganic materials 0.000 abstract description 57
- 239000004332 silver Substances 0.000 abstract description 57
- 239000003795 chemical substances by application Substances 0.000 abstract description 56
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract description 19
- 239000011591 potassium Substances 0.000 abstract description 19
- 229910052700 potassium Inorganic materials 0.000 abstract description 18
- 229910052708 sodium Inorganic materials 0.000 abstract description 18
- 239000000837 restrainer Substances 0.000 abstract description 15
- 238000011161 development Methods 0.000 abstract description 13
- 238000000034 method Methods 0.000 abstract description 11
- 238000009792 diffusion process Methods 0.000 abstract description 10
- 230000008569 process Effects 0.000 abstract description 10
- 238000012546 transfer Methods 0.000 abstract description 10
- 239000012964 benzotriazole Substances 0.000 abstract description 9
- 239000002904 solvent Substances 0.000 abstract description 9
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 abstract description 8
- 150000001875 compounds Chemical class 0.000 abstract description 5
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 18
- 238000012545 processing Methods 0.000 description 12
- 239000000463 material Substances 0.000 description 10
- 150000003839 salts Chemical group 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000000084 colloidal system Substances 0.000 description 9
- 230000001376 precipitating effect Effects 0.000 description 9
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 6
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 5
- 229910000510 noble metal Inorganic materials 0.000 description 5
- 239000000123 paper Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 5
- 235000019345 sodium thiosulphate Nutrition 0.000 description 5
- 229920002554 vinyl polymer Polymers 0.000 description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- 108010010803 Gelatin Proteins 0.000 description 4
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000008273 gelatin Substances 0.000 description 4
- 229920000159 gelatin Polymers 0.000 description 4
- 235000019322 gelatine Nutrition 0.000 description 4
- 235000011852 gelatine desserts Nutrition 0.000 description 4
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 239000002243 precursor Substances 0.000 description 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 3
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 3
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 239000008199 coating composition Substances 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- 125000000623 heterocyclic group Chemical group 0.000 description 3
- 229940071826 hydroxyethyl cellulose Drugs 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 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
- KJUGUADJHNHALS-UHFFFAOYSA-N 1H-tetrazole Substances C=1N=NNN=1 KJUGUADJHNHALS-UHFFFAOYSA-N 0.000 description 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 2
- LAQYHRQFABOIFD-UHFFFAOYSA-N 2-methoxyhydroquinone Chemical compound COC1=CC(O)=CC=C1O LAQYHRQFABOIFD-UHFFFAOYSA-N 0.000 description 2
- 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 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- CKJBFEQMHZICJP-UHFFFAOYSA-N acetic acid;1,3-diaminopropan-2-ol Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.NCC(O)CN CKJBFEQMHZICJP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- XIWMTQIUUWJNRP-UHFFFAOYSA-N amidol Chemical class NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 235000010323 ascorbic acid Nutrition 0.000 description 2
- 229960005070 ascorbic acid Drugs 0.000 description 2
- 239000011668 ascorbic acid Substances 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 229920003090 carboxymethyl hydroxyethyl cellulose Polymers 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 229940105329 carboxymethylcellulose Drugs 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 150000004676 glycans Chemical class 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
- 150000004820 halides Chemical class 0.000 description 2
- 150000002473 indoazoles Chemical class 0.000 description 2
- 150000002916 oxazoles Chemical class 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 2
- 235000019252 potassium sulphite Nutrition 0.000 description 2
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 2
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical compound O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 2
- 150000003230 pyrimidines Chemical class 0.000 description 2
- 239000012260 resinous material Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 2
- 150000003378 silver Chemical class 0.000 description 2
- 235000010265 sodium sulphite Nutrition 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- 230000007480 spreading Effects 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 150000003536 tetrazoles Chemical class 0.000 description 2
- 150000003557 thiazoles Chemical class 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 2
- 150000003852 triazoles Chemical class 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- WGJCBBASTRWVJL-UHFFFAOYSA-N 1,3-thiazolidine-2-thione Chemical compound SC1=NCCS1 WGJCBBASTRWVJL-UHFFFAOYSA-N 0.000 description 1
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 1
- DBCKMJVEAUXWJJ-UHFFFAOYSA-N 2,3-dichlorobenzene-1,4-diol Chemical compound OC1=CC=C(O)C(Cl)=C1Cl DBCKMJVEAUXWJJ-UHFFFAOYSA-N 0.000 description 1
- PFHTYDZPRYLZHX-UHFFFAOYSA-N 2-(2,5-dihydroxyphenyl)benzene-1,4-diol Chemical compound OC1=CC=C(O)C(C=2C(=CC=C(O)C=2)O)=C1 PFHTYDZPRYLZHX-UHFFFAOYSA-N 0.000 description 1
- JHKKTXXMAQLGJB-UHFFFAOYSA-N 2-(methylamino)phenol Chemical class CNC1=CC=CC=C1O JHKKTXXMAQLGJB-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- PHNGKIFUTBFGAG-UHFFFAOYSA-N 2-ethoxybenzene-1,4-diol Chemical compound CCOC1=CC(O)=CC=C1O PHNGKIFUTBFGAG-UHFFFAOYSA-N 0.000 description 1
- QWONTQCJGMKXHJ-UHFFFAOYSA-N 2-methyl-5-(piperidin-1-ylmethyl)benzene-1,4-diol Chemical compound CC1=C(O)C=C(C(=C1)O)CN1CCCCC1 QWONTQCJGMKXHJ-UHFFFAOYSA-N 0.000 description 1
- NYUTUWAFOUJLKI-UHFFFAOYSA-N 3-prop-2-enoyloxypropane-1-sulfonic acid Chemical compound OS(=O)(=O)CCCOC(=O)C=C NYUTUWAFOUJLKI-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
- DSVIHYOAKPVFEH-UHFFFAOYSA-N 4-(hydroxymethyl)-4-methyl-1-phenylpyrazolidin-3-one Chemical compound N1C(=O)C(C)(CO)CN1C1=CC=CC=C1 DSVIHYOAKPVFEH-UHFFFAOYSA-N 0.000 description 1
- KFDVPJUYSDEJTH-UHFFFAOYSA-O 4-ethenylpyridine;hydron Chemical compound C=CC1=CC=[NH+]C=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-O 0.000 description 1
- 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 1
- GDGIVSREGUOIJZ-UHFFFAOYSA-N 5-amino-3h-1,3,4-thiadiazole-2-thione Chemical compound NC1=NN=C(S)S1 GDGIVSREGUOIJZ-UHFFFAOYSA-N 0.000 description 1
- BQCIJWPKDPZNHD-UHFFFAOYSA-N 5-bromo-2h-benzotriazole Chemical compound C1=C(Br)C=CC2=NNN=C21 BQCIJWPKDPZNHD-UHFFFAOYSA-N 0.000 description 1
- MFXKJBZEEFHOQH-UHFFFAOYSA-N 5-methyl-1,3-oxazolidine-2-thione Chemical compound CC1CNC(=S)O1 MFXKJBZEEFHOQH-UHFFFAOYSA-N 0.000 description 1
- WSGURAYTCUVDQL-UHFFFAOYSA-N 5-nitro-1h-indazole Chemical class [O-][N+](=O)C1=CC=C2NN=CC2=C1 WSGURAYTCUVDQL-UHFFFAOYSA-N 0.000 description 1
- 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 1
- XVYRTNNALKOWGM-UHFFFAOYSA-N 6-amino-5-hydroxy-2-methyl-1h-pyrimidin-4-one Chemical compound CC1=NC(=O)C(O)=C(N)N1 XVYRTNNALKOWGM-UHFFFAOYSA-N 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 description 1
- 206010073306 Exposure to radiation Diseases 0.000 description 1
- 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 description 1
- SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 150000000996 L-ascorbic acids Chemical class 0.000 description 1
- 235000011779 Menyanthes trifoliata Nutrition 0.000 description 1
- 240000008821 Menyanthes trifoliata Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- 240000000528 Ricinus communis Species 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 229910021612 Silver iodide Inorganic materials 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
- HOLVRJRSWZOAJU-UHFFFAOYSA-N [Ag].ICl Chemical compound [Ag].ICl HOLVRJRSWZOAJU-UHFFFAOYSA-N 0.000 description 1
- NGDDCFINDCHPTF-UHFFFAOYSA-N [Br].[Ag] Chemical compound [Br].[Ag] NGDDCFINDCHPTF-UHFFFAOYSA-N 0.000 description 1
- FENRSEGZMITUEF-ATTCVCFYSA-E [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].OP(=O)([O-])O[C@@H]1[C@@H](OP(=O)([O-])[O-])[C@H](OP(=O)(O)[O-])[C@H](OP(=O)([O-])[O-])[C@H](OP(=O)(O)[O-])[C@H]1OP(=O)([O-])[O-] Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].OP(=O)([O-])O[C@@H]1[C@@H](OP(=O)([O-])[O-])[C@H](OP(=O)(O)[O-])[C@H](OP(=O)([O-])[O-])[C@H](OP(=O)(O)[O-])[C@H]1OP(=O)([O-])[O-] FENRSEGZMITUEF-ATTCVCFYSA-E 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 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
- 239000000872 buffer Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- JIRRNZWTWJGJCT-UHFFFAOYSA-N carbamothioylthiourea Chemical compound NC(=S)NC(N)=S JIRRNZWTWJGJCT-UHFFFAOYSA-N 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003638 chemical reducing agent 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
- 238000007796 conventional method Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- OAEGRYMCJYIXQT-UHFFFAOYSA-N dithiooxamide Chemical compound NC(=S)C(N)=S OAEGRYMCJYIXQT-UHFFFAOYSA-N 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 238000007757 hot melt coating Methods 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N hydroquinone methyl ether Natural products COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 125000000687 hydroquinonyl group Chemical group C1(O)=C(C=C(O)C=C1)* 0.000 description 1
- 150000002443 hydroxylamines Chemical class 0.000 description 1
- 238000005213 imbibition Methods 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 1
- 229960000367 inositol Drugs 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 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
- 150000002772 monosaccharides Chemical class 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- PLIKAWJENQZMHA-UHFFFAOYSA-N p-hydroxyphenylamine Natural products NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920006324 polyoxymethylene 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
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000033458 reproduction Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 150000003346 selenoethers Chemical class 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
- 229940045105 silver iodide Drugs 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
- HLWRUJAIJJEZDL-UHFFFAOYSA-M sodium;2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetate Chemical compound [Na+].OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC([O-])=O HLWRUJAIJJEZDL-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- WWNBZGLDODTKEM-UHFFFAOYSA-N sulfanylidenenickel Chemical compound [Ni]=S WWNBZGLDODTKEM-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 125000004354 sulfur functional group Chemical group 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 239000002562 thickening agent Substances 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
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000011787 zinc oxide Substances 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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/02—Photosensitive materials characterised by the image-forming section
- G03C8/04—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of inorganic or organo-metallic compounds derived from photosensitive noble metals
- G03C8/06—Silver salt diffusion transfer
Definitions
- a diffusion transfer process comprises developing ah exposed direct positive emulsion in the presence of a silver halide solvent, a silver halide developing agent, a development restrainer such as benzotriazole and sodium and potassium as ions or in combined form e.g. as compounds, including complexes.
- the sodium and potassium are present in a concentration of about 8 to about 27 mole percent potassium and about 92 to about 73 mole percent sodium, based on the total moles of sodium and potassium of about 5 to about 30%, by weight, dry basis of total developing composition.
- This invention concerns diffusion transfer processes, more particularly diffusion transfer processes involving the use of a direct positive silver halide emulsion in the presence of a photographic developing solution containing a development restrainer. It also concerns the processing solution containing a development restrainer and containing both potassium and sodium ions.
- a silver precipitating or nucleating layer generally comprises a binder containing nuclei such as nickel sulfide, colloidal metal and the like.
- Direct positive emulsions are also well known.
- Berriman US. Pat. 3,367,778 describes a direct positive emulsion containing grains comprising a central core of a water insoluble silver salt containing centers which promote the deposition of photolytic silver and an outer shell or covering for such core of a fogged or spontaneously developable water insoluble silver salt.
- Another type of direct positive emulsion is known as a Herschel reversal emulsion in which the silver halide grains have been fogged by previous exposure and are printed by using light of a long wave length which gives a positive image or latent image by destroying parts of the latent image of the fogged areas.
- the processing solution preferably comprises about 0.1 to about 0.44 moles potassium per liter, a thiosulfate silver halide solvent, hydroquinone, 1-phenyl-4,4dimethyl-3- pyrazolidone and about 3 to about 30% by weight based on the total developing agent, dry basis, of a development restrainer.
- the processing solution can be a viscous composition containing a film forming material such as sodium carboxyl methyl cellulose or hydroxyl ethyl cellulose in sufficient quantity to impart to the composition a viscosity of 1,000 to 200,000 centipoises at a temperature of 20 C. It will be appreciated, of course, that the processing composition can be prepared ready to use, in a dry form or in a concentrated form for convenience in handling.
- a transparent receiving sheet such as cellulose acetate, is used having thereon noble metal nuclei. It can also have a diffusion transfer toner such as a water soluble polyvinyl quaternary salt as described in Van Hoff et al. US. Pat. 3,174,858, 4-phenyl-5-imino thiourazole or phenylmercaptotetrazole.
- the processing is carried out by diffusion transfer in which a silver halide complex diffuses from the developing silver halide emulsion to the nucleated receiving sheet where an image is formed having good black tone.
- the process described above is used advantageously to provide a photographic print which is negative with respect to the original light image used to expose the silver halide emulsion and which has excellent transmission density.
- a silver salt direct positive emulsion such as that described in Berriman US. Pat. 3,367,778 issued Feb. 6, 1968 is employed.
- These emulsions contain grains comprising a central core of a water insoluble silver salt containing centers which promote the deposition of photolytic silver and an outer shell or covering for such core of a fogged or spontaneously developable water insoluble silver salt.
- the fogged shell of such grain develops to silver without exposure.
- Suitable direct positive or reversal emulsions include Herschel emulsions in which the emulsion layers have been fogged by a previous exposure to radiation such as ultraviolet, visible or infrared light, or X-rays. The layers give a positive copy by destroying parts of the I latent image of the fogged layer.
- the processing solution has the following components:
- a silver halide solvent such as, for example, sodium thiosulfate, sodium thiocyanate, ammonia or the like present in the quantity required to form a soluble silver complex which diffuses imagewise to the receiving support.
- Silver halide developing agents used for initiating development of the exposed sensitive element can be conventional types used for developing films or papers.
- a developing agent and/or developing agent precursor can be employed in a viscous processing composition containing a thickener such as carboxy methyl cellulose or hydroxy ethyl cellulose imparting a viscosity from 1,000 to 200,000 centipoises at a temperature of 20 C.
- a typical developer composition is disclosed in U.S. Pat. 3,120,795 of Land et al. issued Feb. 11, 1964.
- Developing agents and/or developing agent precursors can be employed alone or in combination with each other, as well as with auxiliary developing agents.
- Suitable silver halide developing agents and developing agent precursors which can be employed include, for example, polyhydroxybenzenes, alkyl substituted hydroquinones, as exemplified by t-butyl hydroquinone, methyl hydroquinone and 2,S-dimethylhydroquinone, catechol and pyrogallol; chloro substituted hydroquinones such as chlorohydroquinone or dichlorohydroquinone; alkoxy substituted hydroquinones such as methoxy hydroquinone or ethoxy hydroquinone; aminophenol developing agents such as 2,4- diaminophenols and methylaminophenols. These include, for example 2,4-diaminophenol developing agents which contain a group in the 6 position, and related amino developing agents.
- the aminophenol developing agents can be employed as an acid salt, such as a hydrochloride or sulf
- silver halide developing agents include ascorbic acid, ascorbic acid derivatives, ascorbic acid ketals, such as those described in U.S. Pat. 3,337,342 of Green issued Aug. 22, 1967; hydroxylamines such as N,N-di(2-ethoxyethyl)-hydroxylarnine; 3-pyrazolidone developing agents such as l-phenyl-3-pyrazolidone, including those described in Kodak British Pat. 930,572 published July 3, 1963; and acyl derivatives of p-aminophenol such as described in Kodak British Patent 1,045,303 published Oct.
- aminomethyl hydroquinone silver halide developing agents such as 2- methyl-S-pyrrolidinomethyl hydroquinone, 2 methyl-S- morpholinomethyl hydroquinone, and 2-methyl-5-piperidinomethyl hydroquinone.
- aminomethyl hydroquinone silver halide developing agents are especially suitable incorporated in the negative photographic element.
- Another suitable silver halide developing agent which can be used in a reductone silver halide developing agent, especially an anhydro dihydroamino hexose reductone silver halide developing agent.
- Lactone derivative silver halide developing agents which have the property of forming a lactone silver halide developing agent precursor under neutral and acid conditions are particularly useful.
- Toning agents are generally present during the diffusion transfer step.
- various toning agents can be contained in the processing solution or even, in some instances, contained in the silver halide emulsion.
- Toning agents which can be included for improving the tone of the image to make the image blacker or more blue-black include selenotetrazoles, including selenotetrazoles substituted by aliphatic residues, as for example, l-allyl-S-seleno- 1,2,3,4-tetrazole, selenotetrazoles substituted by aromatic or heterocyclic residues having l-12 carbon atoms, as for example, l-phenyl-S-seleno-l,2,3,4-tetrazole, etc., sulfur compounds such as 2-mercaptothiazoline, 2-amino-5-mercapto-1,3,4-thiadiazole, 2-thionoimidazolidene, 2-mercapto-5-methyloxazoline, 2 mercapto-S-phenyl-1
- a polymeric toner is used.
- Polymers which are particularly useful are water soluble polyvinyl quaternary salts, as described in Van Hoff et al. U.S. Pat. 3,174,858 issued Mar. 23, 1965. These water soluble basic polymeric quaternary salts have a polyvinyl chain having 2 to 10,000 monomeric units each monomeric unit of which is linked directly to a five or six membered heterocyclic nucleus containing as heteroatoms only nitrogen atoms, one of which heteronitrogen atoms being a quaternary nitrogen atom.
- the polymer has the following structure:
- n is an integer from 2 to 10,000 and X is any suitable anion such as CH SO para toluene sulfonate-', iodide, etc.
- R represents H, and alkyl group having 1 to 10 carbon atoms such as, for example, methyl, ethyl, propyl, butyl, etc., halogen, N0 NH aralkyl, aryl, etc. R is selected from the same group as R, but can be a different group than R. It will be appreciated, of course,
- heterocyclic nucleus can contain additional nitrogen atoms and that the ring may be substituted with other groups.
- the substituents can be the same or different.
- Typical polymeric materials include poly(l,2-dimethyl-5-vinylpyridinium methylsulfate), poly 1,4-vinylpyridinium methylsulfate) poly(1-methyl-Z-vinylpyridinium iodide), poly(1-methyl-2-vinylpyridinium methylsulfate), poly( l-methyl-4-vinylpyridinium iodide), poly(1-methyl-4-vinylpyridinium methylsulfate), poly(1-vinyl-3-methyl imidazolium iodide) and poly(l-vinyl-3-methyl imidazolium methylsulfate).
- the polymer is employed from 0.1 to mg./ft. preferably 0.2 to about 5 mg/ft. In a typical embodiment, 30 mg. of the polyvinyl polymer are used for 1 g. of gel in the receiving layer.
- toners can be used in the amount of about 1.005 to about 5.0 mg./ft. preferably 0.01 to about 1 mg./ft. either in the receiving layer.
- a particularly useful combination employs phenyl mercaptotetrazole and potassium iodide in a developer or activator solution.
- Other toning agents which may be used inlude 5,5'-dithia-bis(l-phenyltetrazole), the S-mercaptotetrazoles of Abbott et al., U.S. Pat. 3,295,971 and Weyde, U.S. Pat. 2,699,393.
- Still other toning agents are disclosed in Tregillus et al. U.S. Pat. 3,017,270 such as 2-thionothiazolidone, 4-phenyliminothiourazo1e, 4-phenyl-1,2,4-triazolidene-3,5-dithione, etc.
- the processing composition contains a development restrainer in an amount of about 1 to about 8 grams per liter of solution or about 3 to about 30%, by weight, based on the total dry weight of silver halide developing agent.
- a development restrainer has a strong inhibiting action on development of latent image silver.
- development restrainers such as benzotriazole, 5-bromobenzotriazole, S-chlorobenzotriazole, S-methylbenzotriazole, 5-nitroindazoles, S-nitrobenzimidazole, etc. can be used.
- development restrainers may be used including triazoles, tetrazoles, oxazoles, thiazoles, pyrimidines, indazoles, tetrazaindenes, pyl'azole, pyrazolone, imidazole, etc.
- Both sodium and potassium are present, preferably in an amount of about 5 to about 30% by weight, dry basis of the total developing composition so that the composition contains about 8 to about 27 mole percent potassium and about 92 to about 73 mole percent sodium, based on total moles of sodium and potassium.
- the alkali metals are present as iOns or in combined form, e.g. as salts such as sodium thiosulfate, potassium sulfite and the like, which compounds may vary widely depending upon the particular purpose for which they are added.
- the pH of the developing solution is preferably within the range of about 10.5 to about 12.5.
- Various means may be used to provide the required pH such as organic bases including 2 methylaminoethanol, diethylaminoethanol and the like and inorganic bases such as sodium hydroxide, potassium hydroxide, and the like may also be used.
- Other addenda include sequestering agents such as ethylenediamine tetraacetic acid, sodium salt; 1,3-diamino 2 propanol tetraacetic acid, etc.
- Water softeners can be added or spreading agents including propylated naphthalene sulfonate, octyl phenoxy polyethyl oxide, sodium hexametaphosphate, etc.
- the receiving sheets which may be used in carrying out the invention include any suitable support having thereon one or more layers at least one layer of which contains a silver precipitant such as silver precipitating nuclei.
- Suitable supports include cellulose esters, polyolefins, polyesters, polyacetals, metal, glass, paper, etc.
- Transparent cellulose ester film support is preferred, such as cellulose acetate.
- Suitable paper supports include any of the conventional paper supports including those prepared from cotton, linen, and wood (sulfate and sulfite pulped). Such supports are typically about 5-60 pounds per 1000 square foot papers.
- the support can have thereon a polymeric material, typically coated in a thickness of about .3 to 5 mils.
- Particularly useful polymeric materials include the polyolefins prepared from the alpha-olefins having 2-10 carbon atoms, blends of these polyolefins and copolymers of the alpha-olefins.
- the coatings may be applied by extrusion or hot melt coating techniques as latexes, as solvent coatings, etc.
- titanium dioxide is incorporated as a pigment in an amount of up to 25%, preferably 10-15% by weight of the resin.
- Other pigments or dyes which may be useful include those commonly known as pigments or dyes for polymeric materials.
- Precipitating agents which are useful in receiving sheets include nuclei which are useful as precipitating agents with a silver halide complex, including all of those nuclei which are commonly useful in the diffusion transfer process.
- Suitable nuclei include silver precipitating agents known in the art such as sulfides, selenides, polysulfides, polyselenides, heavy metals, thiourea, Stannous halides, heavy metal salts, fogged silver halide, Carey Lea silver,
- Noble metal nuclei are particularly active and useful when formed by reducing a noble metal salt using a borohydride or hypophosphite in the presence of a colloid.
- the metal nuclei are prepared in the presence of a hydrophilic colloid such as gelatin and coated on the receiving sheet. The same or a different colloid may be added if desired.
- the coating composition generally contains not only nuclei, but also reaction products which are obtained from reducing the metal salt. Accordingly, the receiving layer can contain the re action by-products which are obtained during the reducing operation.
- the photographic emulsions employed can contain spectral sensitizing dyes such as described in US. Pats. 2,526,632 of Brooker et al. issued Oct. 24, 1950 and 2,503,776 of Sprague issued Apr. 11, 1950.
- Spectral sensitizers which can be used include cyanines, merocyanines, styryls and hemicyanines.
- the photographic emulsions can contain various photographic addenda, particularly those known to be beneficial in photographic compositions.
- Suitable photographic addenda include hardeners, e.g., those set forth in British Pat. 974,317; buffers which maintain the desired developing activity and/ or pH level; coating aids; plasticizers, speed increasing addenda, such as amines, quaternary ammonium salts, sulfonium salts and alkylene oxide polymers; and various stabilizing agents, such as sodium sulfite.
- the photographic silver salt emulsions can be chemically sensitized with compounds of the sulfur group such as sulfur, selenium and tellurium sensitizers, noble metal salts such as gold, or reduction sensitized with reducing agents or combinations of such materials.
- photographic silver salts can be used. These include photographic silver halides such as silver iodide, silver bromine, silver chloride, as well as mixed halides such as silver bromoiodide, silver chloroiodide, silver chlorobromide and silver bromochloroiodide.
- the photographic silver salts are typically contained in an emulsion layer comprising any binding materials suitable for photographic purposes.
- binding materials suitable for photographic purposes.
- These include natural and synthetic binding materials generally employed for this purpose, for example gelatin, colloidal albumin, watersoluble vinyl polymers, mono and polysaccharides, cellulose derivatives, proteins water-soluble polyacrylamides, polyvinyl pyrrolidone and the like, as well as mixtures of such binding agents.
- Stripping agents can be used either on or in the surface of the silver halide emulsion layer, on or in the receiving layer containing the nuclei, or can be contained in the developing or processing solutions. When added to the processing solution in concentrations of about 3% to about 10% by weight, the stripping agents prevent the processing solution from sticking to the receiver. Suitable stripping agents normally are used which have a composition different from the binder used in the silver halide emulsion.
- Typical stripping agents include alkali permeable polysaccharides such as, for example, carboxymethyl cellulose or hydroxyethyl cellulose, 4,4'-dihydroxybiphenol, glucose, sucrose, sorbitol (hexahydric alcohol C H (OH) inositol (hexahydroxy-cyclohexane s d R Z resorcinol, phytic acid sodium salt, thixcin (a castor bean product), zinc oxide, and finely divided polyethylene.
- alkali permeable polysaccharides such as, for example, carboxymethyl cellulose or hydroxyethyl cellulose, 4,4'-dihydroxybiphenol, glucose, sucrose, sorbitol (hexahydric alcohol C H (OH) inositol (hexahydroxy-cyclohexane s d R Z resorcinol, phytic acid sodium salt, thixcin (a castor bean product), zinc oxide, and finely
- a resinous mixed ester lactone release agent is employed as a binder for the silver precipitant in an amount of 1 rug/ft. to about 1 g./ft.
- the resinous material can be combined with a suitable colloid such as a proteinaceous material.
- the resinous material might be coated at a range of 1 mg./ ft. and be combined with gelatin in an amount of 13 mg./ft.
- colloids can be used as dispersing agents or as binders for the precipitating agents in the receiving layer.
- Any suitable colloid can be used.
- Particularly useful colloids are hydrophilic colloids which are used for binders in silver halide emulsions.
- they are coated in a range of about 5 to about 5,000 mg./ft.
- suitable colloids are gelatin, preferably coated at a level in the range of about 7-100 mg./ft.
- polymeric latices such as copoly(2-chloroethylmethacrylate-acrylic acid) preferably coated in the range of "15- 350 mg./ft.
- polymeric vehicle containing two components (1) polyvinyl alcohol, and (2) interpolymer of nbutylacrylate, 3-acryloyloxypropane-l-sulfonic acid, sodium salt and Z-acetoacetoxyethyl methacrylate, in a preferred range of about -300 mg./ft.
- Coating solutions which contain addenda other than a silver precipitant are also useful in preparing receiving layers.
- toners, surfactants, coating aids, developing agents, silver halide solvents, etc. may be added to improve the image quality in the receiving sheet.
- Particularly useful surfactants and spreading agents in receiver coatings include saponin, lauryl alcohol sulfate, p-tert octyl phenoxy ethoxy ethyl sodium sulfonate, etc.
- EXAMPLE 1 A direct positive silver halide emulsion prepared and coated according to Example 1 of Berriman US. Pat. 3,367,778 issued February 6, 1968 is exposed to a light image and contacted with a developer having the following composition:
- Example 3 The process of Example 1 is repeated except that in place of 1-phenyl-4-hydroxymethyl-4-1nethyl-3-pyrazolidone, p-methylamino phenol sulfate is used. A good image is obtained.
- Example 1 is repeated except that in place of l-phenyl- 4-hydroxymethyl-4-methyl-3-pyrazolidone, is used l-phenyl-4,4-dimethyl-3-pyrazolidone. A good image is obtained.
- Example 1 is repeated except that the silver halide emulsion is a Herschel reversal emulsion having layers which have been fogged by previous exposure and which are printed using long wave length light. An image of high transmission density is obtained.
- the silver halide emulsion is a Herschel reversal emulsion having layers which have been fogged by previous exposure and which are printed using long wave length light. An image of high transmission density is obtained.
- a photographic composition for treating a direct positive emulsion comprising a silver halide developing agent, a silver halide solvent, about 3 to about 30%, by weight, based on said developing agent, of a development restrainer and about 5 to about 30%, by weight, dry basis, of sodium and potassium as ions or in combined form, said composition containing about 8 to about 27 mole percent potassium and about 92 to about 73 mole percent sodium in combined or in ionic form, based on total moles of sodium and potassium in said composition.
- a composition of claim 1 in which said restrainer is a member selected from the class consisting of triazoles, indazoles, tetrazaindenes, imidazoles, mercapto compounds, oxazoles, thiazoles, tetrazoles, pyrimidines, pyrazoles and pyrazolones.
- composition of claim 1 in which said restrainer is a benzotriazole is a benzotriazole.
- a liquid composition of claim 1 having a pH in the range of about 10.5 to about 12.5.
- composition of claim 1 in which said silver halide developing agent is 1-phenyl-4-hydr0xymethyl-4-methyl- 3-pyrazolidone.
- composition of claim 1 in which said silver halide developing agent is hydroquinone.
- a composition of claim 1 in which said silver halide developing agent is 1-phenyl-4,4-dimethyl-3-pyrazolidone.
- composition of claim 1 in which the composition is a viscous solution having a viscosity of about 1,000 to about 200,000 centipoises at a temperature of 3,257,205 6/ 1966 Cassiers et a1. 9 695 20 C. 3,418,124 12/1968 Hunt -96-'64 13.
- a composition of claim 1 which further contains 3,458,317 7/1969 Ditzer 9695 an alkylaminoethanol.
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
Abstract
A DIFFUSION TRANSFER PROCESS COMPRISES DEVELOPING AN EXPOSED DIRECT POSITIVE EMULSION IN THE PRESENCE OF A SILVER HALIDE SOLVENT, A SILVER HALIDE DEVELOPING AGENT, A DEVELOPMENT RESTRAINER SUCH AS BENZOTRIAZOLE AND SODIUM AND POTASSIUM AS IONS OR IN COMBINED FORM E.G. AS COMPOUNDS, INCLUDING COMPLEXES. THE SODIUM AND POTASSIUM ARE PRESENT IN A CONCENTRATION OF ABOUT 8 TO ABOUT 27 MOLE PERCENT POTASSIUM AND ABOUT 92 TO ABOUT 73 MOLE PERCENT SODIUM, BASED ON THE TOTAL MOLES OF SODIUM AND POTASSIUM OF ABOUT 5 TO A ABOUT 30%, BY WEIGHT, DRY BASIS OF TOTAL DEVELOPING COMPOSITION.
Description
"United States Patent Ofice 3,733,199 Patented May 15, 1973 3 733 199 PHOTOGRAPHIC COMPOSITION F SODIUM AND POTASSIUM .IONS FOR TREATING DIRECT POSITIVE EMULSIONS Paul E. Crough and Henry J. Snyder, Rochester, N.Y., assignors to Eastman Kodak Company, Rochester, N .Y. No Drawing. Filed June 14, 1971, Ser. No. 152,978 Int. Cl. G03c 5/24 US. CI. 96-64 13 Claims ABSTRACT OF THE DISCLOSURE A diffusion transfer process comprises developing ah exposed direct positive emulsion in the presence of a silver halide solvent, a silver halide developing agent, a development restrainer such as benzotriazole and sodium and potassium as ions or in combined form e.g. as compounds, including complexes. The sodium and potassium are present in a concentration of about 8 to about 27 mole percent potassium and about 92 to about 73 mole percent sodium, based on the total moles of sodium and potassium of about 5 to about 30%, by weight, dry basis of total developing composition.
BACKGROUND OF THE INVENTION This invention concerns diffusion transfer processes, more particularly diffusion transfer processes involving the use of a direct positive silver halide emulsion in the presence of a photographic developing solution containing a development restrainer. It also concerns the processing solution containing a development restrainer and containing both potassium and sodium ions.
Diffusion transfer processes are well known. For example, Rott US. Pat. 2,352,014 describes such a process wherein undeveloped silver halide of an exposed photographic emulsion layer is transferred in a silver complex imagewise by imbibition to a silver precipitating or nucleating layer generally to form a positive image therein. A silver precipitating or nucleating layer generally comprises a binder containing nuclei such as nickel sulfide, colloidal metal and the like.
Direct positive emulsions are also well known. For e ample, Berriman US. Pat. 3,367,778 describes a direct positive emulsion containing grains comprising a central core of a water insoluble silver salt containing centers which promote the deposition of photolytic silver and an outer shell or covering for such core of a fogged or spontaneously developable water insoluble silver salt. Another type of direct positive emulsion is known as a Herschel reversal emulsion in which the silver halide grains have been fogged by previous exposure and are printed by using light of a long wave length which gives a positive image or latent image by destroying parts of the latent image of the fogged areas.
It has been customary to use negative images for various graphic reproductions in which the negative is preposed to the light image after which a suitable transferred image is obtained on a nucleated transparent support. However, an attempt to use a direct positive emulsion resulted in no image being transferred from the direct positive emulsion to the receiving layer using conventional methods.
SUMMARY OF THE INVENTION It has now been found that the aforementioned problems are overcome when the diffusion transfer process employing a direct positive emulsion is carried out in the presence of a silver halide developing agent, a silver halide solvent such as sodium thiosulfate, and a development restrainer such as benzotriazole provided the solution comprises about 8-27 mole percent potassium and about 92- 73 mole percent sodium based on the total moles of potassium and sodium which is generally about 3 to about 30% by weight dry basis of developing composition. The processing solution preferably comprises about 0.1 to about 0.44 moles potassium per liter, a thiosulfate silver halide solvent, hydroquinone, 1-phenyl-4,4dimethyl-3- pyrazolidone and about 3 to about 30% by weight based on the total developing agent, dry basis, of a development restrainer. The processing solution can be a viscous composition containing a film forming material such as sodium carboxyl methyl cellulose or hydroxyl ethyl cellulose in sufficient quantity to impart to the composition a viscosity of 1,000 to 200,000 centipoises at a temperature of 20 C. It will be appreciated, of course, that the processing composition can be prepared ready to use, in a dry form or in a concentrated form for convenience in handling.
In a particularly useful embodiment of the invention, a transparent receiving sheet such as cellulose acetate, is used having thereon noble metal nuclei. It can also have a diffusion transfer toner such as a water soluble polyvinyl quaternary salt as described in Van Hoff et al. US. Pat. 3,174,858, 4-phenyl-5-imino thiourazole or phenylmercaptotetrazole. The processing is carried out by diffusion transfer in which a silver halide complex diffuses from the developing silver halide emulsion to the nucleated receiving sheet where an image is formed having good black tone.
The process described above is used advantageously to provide a photographic print which is negative with respect to the original light image used to expose the silver halide emulsion and which has excellent transmission density.
DESCRIPTION OF PREFERRED EMBODIMENTS In a preferred embodiment, a silver salt direct positive emulsion such as that described in Berriman US. Pat. 3,367,778 issued Feb. 6, 1968 is employed. These emulsions contain grains comprising a central core of a water insoluble silver salt containing centers which promote the deposition of photolytic silver and an outer shell or covering for such core of a fogged or spontaneously developable water insoluble silver salt. The fogged shell of such grain develops to silver without exposure.
Other suitable direct positive or reversal emulsions include Herschel emulsions in which the emulsion layers have been fogged by a previous exposure to radiation such as ultraviolet, visible or infrared light, or X-rays. The layers give a positive copy by destroying parts of the I latent image of the fogged layer.
In a preferred embodiment, the processing solution has the following components:
Water, 1.00 liter. pH, 10.5-12.5.
The components in the above formulation can be varied widely, but it will be appreciated that it is necessary to have a silver halide solvent such as, for example, sodium thiosulfate, sodium thiocyanate, ammonia or the like present in the quantity required to form a soluble silver complex which diffuses imagewise to the receiving support.
Silver halide developing agents used for initiating development of the exposed sensitive element can be conventional types used for developing films or papers. A developing agent and/or developing agent precursor can be employed in a viscous processing composition containing a thickener such as carboxy methyl cellulose or hydroxy ethyl cellulose imparting a viscosity from 1,000 to 200,000 centipoises at a temperature of 20 C. A typical developer composition is disclosed in U.S. Pat. 3,120,795 of Land et al. issued Feb. 11, 1964.
Developing agents and/or developing agent precursors can be employed alone or in combination with each other, as well as with auxiliary developing agents. Suitable silver halide developing agents and developing agent precursors which can be employed include, for example, polyhydroxybenzenes, alkyl substituted hydroquinones, as exemplified by t-butyl hydroquinone, methyl hydroquinone and 2,S-dimethylhydroquinone, catechol and pyrogallol; chloro substituted hydroquinones such as chlorohydroquinone or dichlorohydroquinone; alkoxy substituted hydroquinones such as methoxy hydroquinone or ethoxy hydroquinone; aminophenol developing agents such as 2,4- diaminophenols and methylaminophenols. These include, for example 2,4-diaminophenol developing agents which contain a group in the 6 position, and related amino developing agents. The aminophenol developing agents can be employed as an acid salt, such as a hydrochloride or sulfate salt.
Other silver halide developing agents include ascorbic acid, ascorbic acid derivatives, ascorbic acid ketals, such as those described in U.S. Pat. 3,337,342 of Green issued Aug. 22, 1967; hydroxylamines such as N,N-di(2-ethoxyethyl)-hydroxylarnine; 3-pyrazolidone developing agents such as l-phenyl-3-pyrazolidone, including those described in Kodak British Pat. 930,572 published July 3, 1963; and acyl derivatives of p-aminophenol such as described in Kodak British Patent 1,045,303 published Oct. 12, 1966; pyrimidine developing agents, such as 4-amino- 5,6-dihydroxy-2-methyl pyrimidine; and aminomethyl hydroquinone silver halide developing agents, such as 2- methyl-S-pyrrolidinomethyl hydroquinone, 2 methyl-S- morpholinomethyl hydroquinone, and 2-methyl-5-piperidinomethyl hydroquinone. The aminomethyl hydroquinone silver halide developing agents are especially suitable incorporated in the negative photographic element.
Another suitable silver halide developing agent which can be used in a reductone silver halide developing agent, especially an anhydro dihydroamino hexose reductone silver halide developing agent.
Lactone derivative silver halide developing agents which have the property of forming a lactone silver halide developing agent precursor under neutral and acid conditions are particularly useful.
Toning agents are generally present during the diffusion transfer step. For example, various toning agents can be contained in the processing solution or even, in some instances, contained in the silver halide emulsion. Toning agents which can be included for improving the tone of the image to make the image blacker or more blue-black include selenotetrazoles, including selenotetrazoles substituted by aliphatic residues, as for example, l-allyl-S-seleno- 1,2,3,4-tetrazole, selenotetrazoles substituted by aromatic or heterocyclic residues having l-12 carbon atoms, as for example, l-phenyl-S-seleno-l,2,3,4-tetrazole, etc., sulfur compounds such as 2-mercaptothiazoline, 2-amino-5-mercapto-1,3,4-thiadiazole, 2-thionoimidazolidene, 2-mercapto-5-methyloxazoline, 2 mercapto-S-phenyl-1,3,4-oxadiazole and 2-thionoimidazoline. It will be appreciated that these toners can be used either alone or in conjunction with other toning agents.
In a preferred embodiment, a polymeric toner is used. Polymers which are particularly useful are water soluble polyvinyl quaternary salts, as described in Van Hoff et al. U.S. Pat. 3,174,858 issued Mar. 23, 1965. These water soluble basic polymeric quaternary salts have a polyvinyl chain having 2 to 10,000 monomeric units each monomeric unit of which is linked directly to a five or six membered heterocyclic nucleus containing as heteroatoms only nitrogen atoms, one of which heteronitrogen atoms being a quaternary nitrogen atom.
In one embodiment, the polymer has the following structure:
in which n is an integer from 2 to 10,000 and X is any suitable anion such as CH SO para toluene sulfonate-', iodide, etc. R represents H, and alkyl group having 1 to 10 carbon atoms such as, for example, methyl, ethyl, propyl, butyl, etc., halogen, N0 NH aralkyl, aryl, etc. R is selected from the same group as R, but can be a different group than R. It will be appreciated, of course,
0 that the heterocyclic nucleus can contain additional nitrogen atoms and that the ring may be substituted with other groups. The substituents can be the same or different.
Typical polymeric materials include poly(l,2-dimethyl-5-vinylpyridinium methylsulfate), poly 1,4-vinylpyridinium methylsulfate) poly(1-methyl-Z-vinylpyridinium iodide), poly(1-methyl-2-vinylpyridinium methylsulfate), poly( l-methyl-4-vinylpyridinium iodide), poly(1-methyl-4-vinylpyridinium methylsulfate), poly(1-vinyl-3-methyl imidazolium iodide) and poly(l-vinyl-3-methyl imidazolium methylsulfate).
In a particularly useful coating composition the polymer is employed from 0.1 to mg./ft. preferably 0.2 to about 5 mg/ft. In a typical embodiment, 30 mg. of the polyvinyl polymer are used for 1 g. of gel in the receiving layer.
Typically, other toners can be used in the amount of about 1.005 to about 5.0 mg./ft. preferably 0.01 to about 1 mg./ft. either in the receiving layer. A particularly useful combination employs phenyl mercaptotetrazole and potassium iodide in a developer or activator solution. Other toning agents which may be used inlude 5,5'-dithia-bis(l-phenyltetrazole), the S-mercaptotetrazoles of Abbott et al., U.S. Pat. 3,295,971 and Weyde, U.S. Pat. 2,699,393. Still other toning agents are disclosed in Tregillus et al. U.S. Pat. 3,017,270 such as 2-thionothiazolidone, 4-phenyliminothiourazo1e, 4-phenyl-1,2,4-triazolidene-3,5-dithione, etc.
The processing composition contains a development restrainer in an amount of about 1 to about 8 grams per liter of solution or about 3 to about 30%, by weight, based on the total dry weight of silver halide developing agent. A development restrainer has a strong inhibiting action on development of latent image silver. In the preferred embodiments, development restrainers such as benzotriazole, 5-bromobenzotriazole, S-chlorobenzotriazole, S-methylbenzotriazole, 5-nitroindazoles, S-nitrobenzimidazole, etc. can be used. However, other development restrainers may be used including triazoles, tetrazoles, oxazoles, thiazoles, pyrimidines, indazoles, tetrazaindenes, pyl'azole, pyrazolone, imidazole, etc.
Both sodium and potassium are present, preferably in an amount of about 5 to about 30% by weight, dry basis of the total developing composition so that the composition contains about 8 to about 27 mole percent potassium and about 92 to about 73 mole percent sodium, based on total moles of sodium and potassium. It will be appreciated that the alkali metals are present as iOns or in combined form, e.g. as salts such as sodium thiosulfate, potassium sulfite and the like, which compounds may vary widely depending upon the particular purpose for which they are added.
The pH of the developing solution is preferably within the range of about 10.5 to about 12.5.
Various means may be used to provide the required pH such as organic bases including 2 methylaminoethanol, diethylaminoethanol and the like and inorganic bases such as sodium hydroxide, potassium hydroxide, and the like may also be used. Other addenda include sequestering agents such as ethylenediamine tetraacetic acid, sodium salt; 1,3-diamino 2 propanol tetraacetic acid, etc. Water softeners can be added or spreading agents including propylated naphthalene sulfonate, octyl phenoxy polyethyl oxide, sodium hexametaphosphate, etc.
The receiving sheets which may be used in carrying out the invention include any suitable support having thereon one or more layers at least one layer of which contains a silver precipitant such as silver precipitating nuclei. Suitable supports include cellulose esters, polyolefins, polyesters, polyacetals, metal, glass, paper, etc. Transparent cellulose ester film support is preferred, such as cellulose acetate.
Suitable paper supports include any of the conventional paper supports including those prepared from cotton, linen, and wood (sulfate and sulfite pulped). Such supports are typically about 5-60 pounds per 1000 square foot papers.
The support can have thereon a polymeric material, typically coated in a thickness of about .3 to 5 mils. Particularly useful polymeric materials include the polyolefins prepared from the alpha-olefins having 2-10 carbon atoms, blends of these polyolefins and copolymers of the alpha-olefins. The coatings may be applied by extrusion or hot melt coating techniques as latexes, as solvent coatings, etc.
In some instances it is desirable to incorporate in the polymeric material at least one pigment or dye, especially where a white background is required but this is not required. In a particularly useful embodiment, titanium dioxide is incorporated as a pigment in an amount of up to 25%, preferably 10-15% by weight of the resin. Other pigments or dyes which may be useful include those commonly known as pigments or dyes for polymeric materials.
Precipitating agents which are useful in receiving sheets include nuclei which are useful as precipitating agents with a silver halide complex, including all of those nuclei which are commonly useful in the diffusion transfer process. Suitable nuclei include silver precipitating agents known in the art such as sulfides, selenides, polysulfides, polyselenides, heavy metals, thiourea, Stannous halides, heavy metal salts, fogged silver halide, Carey Lea silver,
and complex salts of heavy metals with a compound such as thioacetamide, dithiooxamide and dithiobiuret. As examples of suitable silver precipitating agents and of imagereceiving elements containing such silver precipitating agents, reference may be made to US. Pats. 2,698,237, 2,698,238 and 2,698,245 issued to Edwin H. Land on Dec. 28, 1954, US. Pat. 2,774,667 issued to Edwin H. Land and Meroe M. Morse on Dec. 18, 1956, US. Pat. 2,823,122 issued to Edwin H. Land on Feb. 11, 1958, U8. Pat. 3,396,018 issued to Beavers et a1. Aug. 6, 1968 and also US. Pat. 3,369,901 issued to Fogg et al. Feb. 20, 196 8. The noble metals, silver, gold, platinum, palladium, etc., in the colloidal form are particularly useful.
Noble metal nuclei are particularly active and useful when formed by reducing a noble metal salt using a borohydride or hypophosphite in the presence of a colloid. The metal nuclei are prepared in the presence of a hydrophilic colloid such as gelatin and coated on the receiving sheet. The same or a different colloid may be added if desired. It will be appreciated that the coating composition generally contains not only nuclei, but also reaction products which are obtained from reducing the metal salt. Accordingly, the receiving layer can contain the re action by-products which are obtained during the reducing operation.
The photographic emulsions employed can contain spectral sensitizing dyes such as described in US. Pats. 2,526,632 of Brooker et al. issued Oct. 24, 1950 and 2,503,776 of Sprague issued Apr. 11, 1950. Spectral sensitizers which can be used include cyanines, merocyanines, styryls and hemicyanines.
The photographic emulsions can contain various photographic addenda, particularly those known to be beneficial in photographic compositions. Various addenda and concentrations to be employed can be determined by those skilled in the art. Suitable photographic addenda include hardeners, e.g., those set forth in British Pat. 974,317; buffers which maintain the desired developing activity and/ or pH level; coating aids; plasticizers, speed increasing addenda, such as amines, quaternary ammonium salts, sulfonium salts and alkylene oxide polymers; and various stabilizing agents, such as sodium sulfite. The photographic silver salt emulsions can be chemically sensitized with compounds of the sulfur group such as sulfur, selenium and tellurium sensitizers, noble metal salts such as gold, or reduction sensitized with reducing agents or combinations of such materials.
Various photographic silver salts can be used. These include photographic silver halides such as silver iodide, silver bromine, silver chloride, as well as mixed halides such as silver bromoiodide, silver chloroiodide, silver chlorobromide and silver bromochloroiodide.
The photographic silver salts are typically contained in an emulsion layer comprising any binding materials suitable for photographic purposes. These include natural and synthetic binding materials generally employed for this purpose, for example gelatin, colloidal albumin, watersoluble vinyl polymers, mono and polysaccharides, cellulose derivatives, proteins water-soluble polyacrylamides, polyvinyl pyrrolidone and the like, as well as mixtures of such binding agents.
Stripping agents can be used either on or in the surface of the silver halide emulsion layer, on or in the receiving layer containing the nuclei, or can be contained in the developing or processing solutions. When added to the processing solution in concentrations of about 3% to about 10% by weight, the stripping agents prevent the processing solution from sticking to the receiver. Suitable stripping agents normally are used which have a composition different from the binder used in the silver halide emulsion. Typical stripping agents include alkali permeable polysaccharides such as, for example, carboxymethyl cellulose or hydroxyethyl cellulose, 4,4'-dihydroxybiphenol, glucose, sucrose, sorbitol (hexahydric alcohol C H (OH) inositol (hexahydroxy-cyclohexane s d R Z resorcinol, phytic acid sodium salt, thixcin (a castor bean product), zinc oxide, and finely divided polyethylene. These coatings are relatively thin having a preferred coverage of about 6.0 mg./ft. However, a useful range may be from 1.0 mg. to 1.0 g./ft.
In one embodiment a resinous mixed ester lactone release agent is employed as a binder for the silver precipitant in an amount of 1 rug/ft. to about 1 g./ft. It will be appreciated that when smaller amounts are used, that the resinous material can be combined with a suitable colloid such as a proteinaceous material. For example, the resinous material might be coated at a range of 1 mg./ ft. and be combined with gelatin in an amount of 13 mg./ft.
Various colloids can be used as dispersing agents or as binders for the precipitating agents in the receiving layer. Any suitable colloid can be used. Particularly useful colloids are hydrophilic colloids which are used for binders in silver halide emulsions. Advantageously, they are coated in a range of about 5 to about 5,000 mg./ft. Included among suitable colloids are gelatin, preferably coated at a level in the range of about 7-100 mg./ft. polymeric latices such as copoly(2-chloroethylmethacrylate-acrylic acid) preferably coated in the range of "15- 350 mg./ft. a polymeric vehicle containing two components (1) polyvinyl alcohol, and (2) interpolymer of nbutylacrylate, 3-acryloyloxypropane-l-sulfonic acid, sodium salt and Z-acetoacetoxyethyl methacrylate, in a preferred range of about -300 mg./ft.
Coating solutions which contain addenda other than a silver precipitant are also useful in preparing receiving layers. In addition to various components contained in the coating composition according to this invention, toners, surfactants, coating aids, developing agents, silver halide solvents, etc., may be added to improve the image quality in the receiving sheet.
Particularly useful surfactants and spreading agents in receiver coatings include saponin, lauryl alcohol sulfate, p-tert octyl phenoxy ethoxy ethyl sodium sulfonate, etc.
The following examples are included for a further understanding of the invention:
EXAMPLE 1 A direct positive silver halide emulsion prepared and coated according to Example 1 of Berriman US. Pat. 3,367,778 issued February 6, 1968 is exposed to a light image and contacted with a developer having the following composition:
2-methylaminoethanol ml 27 Diethylaminoethanol ml 74 Potassium sulfite 45% solution ml 27 Sodium hydroxide gm 7 Sodium sulfite gm 46 Hydroquinone gm 18 1-phenyl-4-hydroxymethyl-4 methyl 3 pyrazolidone gm 3.0 1,3-diamino-2-propanol tetraacetic acid gm 0.5 Benzotriazole gm 3.0 Sodium thiosulfate gm 35.0 2-mercapto-5-phenyl-1,3,4-oxadiazole gm 0.10 Natrosol 250H (hydroxyethylcellulose) gm 1.5 Water, 1.00 liter. pH 1135305 While the emulsion is developing, it is contacted against a transparent receiving sheet having thereon palladium nuclei. The resulting image has a high transmission density and good contrast.
When benzotriazole is omitted from the above formulation, no image is obtained. When benzotriazole is included in an amount of about 2% by weight based on total developing agent, no image is obtained. When potassium ion is omitted from the formulation, no image is obtained.
EXAMPLE 2 Example 1 is repeated using the same formulation except instead of benzotriazole each of the following is used in the same amount:
5-brombenzotriazole 5-chlorobenzotriazole S-methylbenzotriazole S-nitroindazole S-nitrobenzimidazole Good images are obtained.
EXAMPLE 3 The process of Example 1 is repeated except that in place of 1-phenyl-4-hydroxymethyl-4-1nethyl-3-pyrazolidone, p-methylamino phenol sulfate is used. A good image is obtained.
EXAMPLE 4 Example 1 is repeated except that in place of l-phenyl- 4-hydroxymethyl-4-methyl-3-pyrazolidone, is used l-phenyl-4,4-dimethyl-3-pyrazolidone. A good image is obtained.
EXAMPLE 5 Example 1 is repeated except that the silver halide emulsion is a Herschel reversal emulsion having layers which have been fogged by previous exposure and which are printed using long wave length light. An image of high transmission density is obtained.
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 effected within the spirit and scope of the invention.
We claim:
1. A photographic composition for treating a direct positive emulsion comprising a silver halide developing agent, a silver halide solvent, about 3 to about 30%, by weight, based on said developing agent, of a development restrainer and about 5 to about 30%, by weight, dry basis, of sodium and potassium as ions or in combined form, said composition containing about 8 to about 27 mole percent potassium and about 92 to about 73 mole percent sodium in combined or in ionic form, based on total moles of sodium and potassium in said composition.
2. A composition of claim 1 in which said restrainer is a member selected from the class consisting of triazoles, indazoles, tetrazaindenes, imidazoles, mercapto compounds, oxazoles, thiazoles, tetrazoles, pyrimidines, pyrazoles and pyrazolones.
3. A composition of claim 1 in which said restrainer is a benzotriazole.
4. A composition of claim 1 in which said restrainer is an indazole.
5. A composition of claim 1 in which said restrainer is an imidazole.
6. A liquid composition of claim 1 having a pH in the range of about 10.5 to about 12.5.
7. A composition of claim 1 in which said developing agent is a mixture of a polyhydroxybenzene developing agent and a 3-pyrazolidone developing agent.
8. A composition of claim 1 in which said silver halide developing agent is 1-phenyl-4-hydr0xymethyl-4-methyl- 3-pyrazolidone.
9. A composition of claim 1 in which said silver halide developing agent is hydroquinone.
10. A composition of claim 1 in which said silver halide developing agent is 1-phenyl-4,4-dimethyl-3-pyrazolidone.
11. A composition of claim 1 in which said silver halide solvent is sodium thiosulfate.
12. A composition of claim 1 in which the composition is a viscous solution having a viscosity of about 1,000 to about 200,000 centipoises at a temperature of 3,257,205 6/ 1966 Cassiers et a1. 9 695 20 C. 3,418,124 12/1968 Hunt -96-'64 13. A composition of claim 1 which further contains 3,458,317 7/1969 Ditzer 9695 an alkylaminoethanol.
5 NORMAN G. TORCHIN, Primary Examiner References Cted J. L. GOODROW, Assistant Examiner UNITED STATES PATENTS 3,260,598 7/1966 Yutzy et a1. 9 6-95 3,345,174 10/1967 Dotson e161. 9695 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15297871A | 1971-06-14 | 1971-06-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3733199A true US3733199A (en) | 1973-05-15 |
Family
ID=22545259
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00152978A Expired - Lifetime US3733199A (en) | 1971-06-14 | 1971-06-14 | Photographic composition of sodium and potassium ions for treating direct positive emulsions |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3733199A (en) |
| CA (1) | CA962500A (en) |
| FR (1) | FR2141885B1 (en) |
| GB (1) | GB1401044A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4309499A (en) * | 1978-11-14 | 1982-01-05 | Fuji Photo Film Co., Ltd. | Formation of black-and-white silver-containing negative images by a diffusion transfer process |
| US4359397A (en) * | 1980-12-31 | 1982-11-16 | Polaroid Corporation | Benzotriazole complexes and film units employing same |
| US4418139A (en) * | 1980-12-31 | 1983-11-29 | Polaroid Corporation | Film units containing thermally induced water-releasing benzotriazole complex |
| JPS6173953A (en) * | 1984-09-20 | 1986-04-16 | Mitsubishi Paper Mills Ltd | Processing solution for silver complex diffusion transfer |
| JPS6173951A (en) * | 1984-09-20 | 1986-04-16 | Mitsubishi Paper Mills Ltd | Processing solution for silver complex diffusion transfer |
| JPS6173950A (en) * | 1984-09-20 | 1986-04-16 | Mitsubishi Paper Mills Ltd | Processing solution for silver complex diffusion transfer |
| US4987060A (en) * | 1989-04-03 | 1991-01-22 | Minnesota Mining And Manufacturing Company | Concentrated photographic developer composition and method of making it |
-
1971
- 1971-06-14 US US00152978A patent/US3733199A/en not_active Expired - Lifetime
-
1972
- 1972-05-08 CA CA141,543A patent/CA962500A/en not_active Expired
- 1972-06-14 FR FR7221312A patent/FR2141885B1/fr not_active Expired
- 1972-06-14 GB GB2774172A patent/GB1401044A/en not_active Expired
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4309499A (en) * | 1978-11-14 | 1982-01-05 | Fuji Photo Film Co., Ltd. | Formation of black-and-white silver-containing negative images by a diffusion transfer process |
| US4359397A (en) * | 1980-12-31 | 1982-11-16 | Polaroid Corporation | Benzotriazole complexes and film units employing same |
| US4418139A (en) * | 1980-12-31 | 1983-11-29 | Polaroid Corporation | Film units containing thermally induced water-releasing benzotriazole complex |
| JPS6173953A (en) * | 1984-09-20 | 1986-04-16 | Mitsubishi Paper Mills Ltd | Processing solution for silver complex diffusion transfer |
| JPS6173951A (en) * | 1984-09-20 | 1986-04-16 | Mitsubishi Paper Mills Ltd | Processing solution for silver complex diffusion transfer |
| JPS6173950A (en) * | 1984-09-20 | 1986-04-16 | Mitsubishi Paper Mills Ltd | Processing solution for silver complex diffusion transfer |
| US4987060A (en) * | 1989-04-03 | 1991-01-22 | Minnesota Mining And Manufacturing Company | Concentrated photographic developer composition and method of making it |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1401044A (en) | 1975-07-16 |
| FR2141885A1 (en) | 1973-01-26 |
| FR2141885B1 (en) | 1977-12-23 |
| CA962500A (en) | 1975-02-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3647440A (en) | Photographic diffusion transfer product and process | |
| JPS5931694B2 (en) | Method for forming black and white negative silver images using diffusion transfer photography | |
| US4242436A (en) | Photographic material for continuous tone reproduction | |
| GB2132371A (en) | Spectrally sensitized inner latent image type silver halide photographic emulsions | |
| US3733199A (en) | Photographic composition of sodium and potassium ions for treating direct positive emulsions | |
| JPS5851257B2 (en) | Processing liquid composition for silver complex diffusion transfer | |
| US4147543A (en) | Developer compositions for high contrast diffusion transfer photographic materials and process therefor | |
| US4436805A (en) | Silver complex diffusion transfer process using two toning agents | |
| US3985561A (en) | Diffusion transfer process using silver halide emulsions with 90% chloride and high binder to silver halide ratios | |
| US3619186A (en) | Photographic diffusion transfer product and process | |
| EP0397925A1 (en) | Processing liquid for use in DTR-photography | |
| US3706568A (en) | Photographic diffusion transfer product and process | |
| US3723126A (en) | Photographic developers with titanous diethylenetriaminepentaacetic acid | |
| US3698900A (en) | Diffusion transfer process utilizing 2-mercapto imidazoles | |
| US3563740A (en) | Use of dicyanamides in and with photosensitive systems | |
| EP0187879A1 (en) | Method and material for the production of continuous tone silver images by the silver complex diffusion transfer reversal process | |
| US3236642A (en) | Process for producing direct positives by the silver salt diffusion process | |
| EP0135786B1 (en) | Photographic image receiving elements for silver salt diffusion transfer processes | |
| US3620728A (en) | Receiving sheet for diffusion transfer processes | |
| US3672891A (en) | Photographic element and process comprising a pyrimidine silver halide developing agent | |
| US3565619A (en) | Photographic image transfer process utilizing imidazolidine-2-thione | |
| US3655380A (en) | Diffusion transfer product and process containing 5-seleno-1,2,3,4-tetrazole | |
| US4310613A (en) | Liquid processing composition for silver complex diffusion transfer process | |
| US3600171A (en) | Sulfonamides in diffusion transfer systems | |
| US4298677A (en) | Diffusion transfer photographic process |