JPH0353244A - Developing solution for silver halide photographic sensitive material - Google Patents
Developing solution for silver halide photographic sensitive materialInfo
- Publication number
- JPH0353244A JPH0353244A JP18626589A JP18626589A JPH0353244A JP H0353244 A JPH0353244 A JP H0353244A JP 18626589 A JP18626589 A JP 18626589A JP 18626589 A JP18626589 A JP 18626589A JP H0353244 A JPH0353244 A JP H0353244A
- Authority
- JP
- Japan
- Prior art keywords
- developer
- group
- silver
- developing
- silver halide
- 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.)
- Granted
Links
- 229910052709 silver Inorganic materials 0.000 title claims abstract description 44
- 239000004332 silver Substances 0.000 title claims abstract description 44
- 239000000463 material Substances 0.000 title claims abstract description 24
- -1 silver halide Chemical class 0.000 title claims description 29
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract 2
- 125000003396 thiol group Chemical group [H]S* 0.000 claims abstract 2
- 150000001875 compounds Chemical class 0.000 claims description 20
- 239000000126 substance Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 abstract description 24
- 239000010802 sludge Substances 0.000 abstract description 20
- 238000012545 processing Methods 0.000 abstract description 10
- 238000011109 contamination Methods 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 description 18
- 239000000243 solution Substances 0.000 description 17
- 239000003795 chemical substances by application Substances 0.000 description 11
- 238000011161 development Methods 0.000 description 11
- 239000000839 emulsion Substances 0.000 description 10
- 239000010410 layer Substances 0.000 description 9
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 5
- 239000010931 gold Substances 0.000 description 5
- 229910052737 gold Inorganic materials 0.000 description 5
- 229910021607 Silver chloride Inorganic materials 0.000 description 4
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical group [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 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 3
- 238000011282 treatment Methods 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 206010070834 Sensitisation Diseases 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 238000000586 desensitisation Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 239000008273 gelatin Substances 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 230000005070 ripening Effects 0.000 description 2
- 230000008313 sensitization Effects 0.000 description 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 235000010265 sodium sulphite Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
- CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 2
- 239000012224 working solution Substances 0.000 description 2
- LUMLZKVIXLWTCI-NSCUHMNNSA-N (e)-2,3-dichloro-4-oxobut-2-enoic acid Chemical compound OC(=O)C(\Cl)=C(/Cl)C=O LUMLZKVIXLWTCI-NSCUHMNNSA-N 0.000 description 1
- OHBQPCCCRFSCAX-UHFFFAOYSA-N 1,4-Dimethoxybenzene Chemical compound COC1=CC=C(OC)C=C1 OHBQPCCCRFSCAX-UHFFFAOYSA-N 0.000 description 1
- MEKOFIRRDATTAG-UHFFFAOYSA-N 2,2,5,8-tetramethyl-3,4-dihydrochromen-6-ol Chemical compound C1CC(C)(C)OC2=C1C(C)=C(O)C=C2C MEKOFIRRDATTAG-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
- YKUDHBLDJYZZQS-UHFFFAOYSA-N 2,6-dichloro-1h-1,3,5-triazin-4-one Chemical compound OC1=NC(Cl)=NC(Cl)=N1 YKUDHBLDJYZZQS-UHFFFAOYSA-N 0.000 description 1
- BDOYKFSQFYNPKF-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetic acid;sodium Chemical compound [Na].[Na].OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O BDOYKFSQFYNPKF-UHFFFAOYSA-N 0.000 description 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 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
- LRUDIIUSNGCQKF-UHFFFAOYSA-N 5-methyl-1H-benzotriazole Chemical compound C1=C(C)C=CC2=NNN=C21 LRUDIIUSNGCQKF-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- 208000002109 Argyria Diseases 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
- XCFIVNQHHFZRNR-UHFFFAOYSA-N [Ag].Cl[IH]Br Chemical compound [Ag].Cl[IH]Br XCFIVNQHHFZRNR-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 235000011126 aluminium potassium sulphate Nutrition 0.000 description 1
- XIWMTQIUUWJNRP-UHFFFAOYSA-N amidol Chemical compound NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 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
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- HDFRDWFLWVCOGP-UHFFFAOYSA-N carbonothioic O,S-acid Chemical compound OC(S)=O HDFRDWFLWVCOGP-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000002738 chelating 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
- 239000011248 coating agent Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- BXJGUBZTZWCMEX-UHFFFAOYSA-N dimethylhydroquinone Natural products CC1=C(C)C(O)=CC=C1O BXJGUBZTZWCMEX-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 150000002085 enols Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000035558 fertility Effects 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 150000004820 halides Chemical class 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
- 150000004679 hydroxides Chemical class 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- ZAKLKBFCSHJIRI-UHFFFAOYSA-N mucochloric acid Natural products OC1OC(=O)C(Cl)=C1Cl ZAKLKBFCSHJIRI-UHFFFAOYSA-N 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229940050271 potassium alum Drugs 0.000 description 1
- GNHOJBNSNUXZQA-UHFFFAOYSA-J potassium aluminium sulfate dodecahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.O.O.[Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GNHOJBNSNUXZQA-UHFFFAOYSA-J 0.000 description 1
- RWPGFSMJFRPDDP-UHFFFAOYSA-L potassium metabisulfite Chemical compound [K+].[K+].[O-]S(=O)S([O-])(=O)=O RWPGFSMJFRPDDP-UHFFFAOYSA-L 0.000 description 1
- 229940043349 potassium metabisulfite Drugs 0.000 description 1
- 235000010263 potassium metabisulphite Nutrition 0.000 description 1
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
- 235000019252 potassium sulphite Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、ハロゲン化銀写真感光材料の現像処埋方法に
関し、特にそれに用いる現像液に関するものである。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for developing silver halide photographic materials, and particularly to a developer used therein.
(従来技術)
一般に、ハロゲン化銀写真感光材料の現像処理に用いら
れる現像液中には現像液の保存安定性を高める目的で亜
硫酸塩を含むことは周知である。(Prior Art) It is well known that a developer used for developing silver halide photographic materials generally contains a sulfite salt for the purpose of improving the storage stability of the developer.
また場合によっては、例えば銀塩拡散転写用現像液や一
浴現像定着液のようにチオ硫酸塩のようなハロゲン化銀
に対して溶解作用の強い化合物を含む現像液も用いられ
る。In some cases, a developer containing a compound having a strong dissolving action on silver halide, such as thiosulfate, is also used, such as a developer for silver salt diffusion transfer or a one-bath development fixer.
これら亜硫酸塩やチオ硫酸塩のようなハロゲン化銀に対
して溶解作用を有する化合物を含む現像液で感光材料を
処理すると多量の銀錯体が現像液中に溶出し、溶出した
銀錯体は容易に還元されて銀スラツジとなって蓄積され
る。特に自動現像機を用いて継続的に感光材料を処理す
る場合には、銀スラツジが浮遊するだけでなく、ローラ
やベルト等に付着し,感光材料にローラ筋状の銀スティ
ンと称する光の反射により黄色あるいは褐色金呈する析
出銀による汚れが発生する。When a photosensitive material is processed with a developer containing a compound that has a dissolving effect on silver halide, such as sulfite or thiosulfate, a large amount of silver complex is eluted into the developer, and the eluted silver complex is easily removed. It is reduced and accumulated as silver sludge. In particular, when photosensitive materials are continuously processed using automatic processors, silver sludge not only floats, but also adheres to rollers, belts, etc., and reflects light on the photosensitive materials, called roller streaks, called silver stains. As a result, stains caused by precipitated silver that appear yellow or brown-gold occur.
銀スラツジや液汚れの防止剤として、2−メルカブ}
− 1. 3. 4−チアジアゾール類(英国特許第9
40169号BJI細誉)、2−メルカブト−1.3.
4−オキサジアゾール類あるいは1−7エニルー5−メ
ルカブトテトラゾール(米国特許13,173,789
号明細曹)、D.L.−6.8−ジチオオクタン酸(米
国特許弟3,3 1 8,7 0 1号明細書)、0メ
ルカブト安息香酸(英国特許第1144481号[男a
曹)、脂肪族メルカプトカルボン酸(米国特wr弟3,
6 2 8,9 5 5号明細書)、L−チ77”リジ
7−4−−jJkボン酸( J.Photogr. S
ci.,13.233rl965))、ジスルフイド化
合物C%開昭52−36029号明細省)、2−ペンゾ
オキサゾールチオール、2−ペンゾイミダゾールチオー
ル( Photogr. Sci. Eng.. 20
, 220 (197 6 ))、アセチレングリコー
ル類C%lltJ昭55−95947号明#IW)、2
−メルカプトペンゾチアゾール−5スルホン酸←特開昭
56−72441号四細8)等が知ら力,ている。2-Merkab} as an agent to prevent silver sludge and liquid stains
-1. 3. 4-Thiadiazoles (British Patent No. 9)
No. 40169 BJI Honor), 2-Merkabuto-1.3.
4-oxadiazoles or 1-7 enyl-5-mercabutotetrazole (U.S. Pat. No. 13,173,789)
D. L. -6,8-dithiooctanoic acid (U.S. Patent No. 3,318,701), 0-mercabutobenzoic acid (British Patent No. 1144481 [Male
Cao), aliphatic mercaptocarboxylic acid (US special wr brother 3,
6 2 8, 9 5 5), L-thi 77"lidi 7-4--jJk bolic acid (J. Photogr. S
ci. , 13.233rl965)), disulfide compound C% 1987-36029), 2-penzoxazolethiol, 2-penzimidazolethiol (Photogr. Sci. Eng.. 20
, 220 (1976)), Acetylene Glycols C%lltJ No. 55-95947 Akira #IW), 2
-Mercaptopenzothiazole-5 sulfonic acid ← JP-A-56-72441 8) etc. are known.
しかしながら、これらの化合物は、ハロゲン化銀に対し
て溶解作用を有する現像液、特に高濃度の亜硫酸塩(例
えば0.2モル/t以上)を含む現像液においてスラツ
ジ防止剤として使用した場合、空気酸化によりスラッジ
防止効果を失ったり、スラツジ防止効果が弱く多量の使
用が必要であったり、減感や軟調化、現像抑制などの写
真特性に悪影w’t与えたり、その他高価であったり、
不快臭を有していたりして、充分満足できるものとは言
い難いという問題があった。However, when these compounds are used as sludge inhibitors in a developer having a dissolving action on silver halide, especially a developer containing a high concentration of sulfite (e.g. 0.2 mol/t or more), air The sludge prevention effect may be lost due to oxidation, the sludge prevention effect may be weak and a large amount must be used, it may have negative effects on photographic properties such as desensitization, softening, and development suppression, or it may be expensive.
There was a problem that it was difficult to say that it was completely satisfactory because it had an unpleasant odor.
(発明が解決しようとする課題)
従って、本発明の目的は、ハロゲン化銀に対して溶解作
用を有する現像液、特に高濃度の亜&t酸塩を含む安定
な現像液により自動現像機金用いて感光材料を処理する
ときに、銀スラツジによる液汚れや現像機のローラやベ
ルトの汚れを防ぎ、銀ステインのない仕上り品質の優れ
た写真画像を得ることが出来る現像液を提供することに
ある。(Problems to be Solved by the Invention) Therefore, an object of the present invention is to use a developing solution having a dissolving action on silver halide, particularly a stable developing solution containing a high concentration of &t salt, for use in an automatic developing machine. The purpose of the present invention is to provide a developing solution that prevents liquid stains caused by silver sludge and stains on the rollers and belts of a developing machine when processing photosensitive materials, and that can obtain photographic images with excellent finished quality and no silver stains. .
本発明の別の目的は、前述した問題が無く銀スラツジの
発生を防止した現像液でハロゲン化銀黒白写真感光材料
を処理する方法を提供することにある。Another object of the present invention is to provide a method for processing silver halide black-and-white photographic materials with a developer that does not have the above-mentioned problems and prevents the generation of silver sludge.
(課題を解決するためO手段)
本発明の上記目的は、ハロゲンイヒ銀写真感光材料用現
像液に下記一般式〔I〕で表わされる化合物を含有する
ことによって達成された。(O Means for Solving the Problems) The above object of the present invention was achieved by containing a compound represented by the following general formula [I] in a developer for silver halide photographic light-sensitive materials.
C式中、A及びBは、メルヵブト基、ヒドロキシす。R
1及び凡2は、水素原子、−X−Y基を表わし、Xは2
価基を表わし、Yはカルボキシル基、ヒドロキシル基金
表わす。)
以下に前記一般式(1)で表わされる化合物の具体例を
示す。但し、A及びBのみを示している。In formula C, A and B are a mercabuto group and a hydroxy group. R
1 and 2 represent a hydrogen atom or a -X-Y group, and X is 2
Y represents a carboxyl group or a hydroxyl group. ) Specific examples of the compound represented by the general formula (1) are shown below. However, only A and B are shown.
これらの化合物は、公知であり、例えば特聞昭58−1
05231号、同昭59−9661号明aI誓などを参
照することができる。These compounds are publicly known, for example,
Reference may be made to No. 05231 and No. 59-9661 of the same.
一般式CI)で表わされる化合物の添加証は、現像液1
t当り約o.oos〜約52、好筐し〈は約0.01〜
約22の範囲である。The proof of addition of the compound represented by the general formula CI) is as follows: developer solution 1
Approximately o. oos ~ approx. 52, good case < approx. 0.01 ~
The range is approximately 22.
本発四の現低処理液は、通常の黒白写真用現像生薬例え
ばハイドロキノン、アルキルノ1イドロキノン(例えば
t−ブチルノ1イドロキノン、メチルハイドロキノン、
ジメチルノ\イドロキノン)、カテコール、ピラゾール
、クロロハイドロキノン、ジクロロハイドロキノン、ア
ルコキシノ・イドロキノン(例えばメトキシ又はエトキ
シノ・イドロキノン)、アミノンエノール現像生薬C例
えばN−メチルーp−アミノンエノール、2.4−ジア
ミノフェノール)、アスコルビン酸現像主朶、N−メチ
ルーp−アミノフェノールサルフエート、ビラゾロン類
(例えば4−アミノビラゾロン)、3−ビラゾリドン現
像王薬(例えば1−7エニル−3−ビラゾリドン、1−
フエニル−4.4−ジメチル−3−ビラソリドン,1−
7エニルー5−メチル−3 − ヒラ7” IJドン、
1−7エニルー4−メチルー3−ビラゾリドン、1.5
−ジ7エニル−3−ビラゾリドン,1−p−}リルー3
−ビラゾリドン、1−フエニル−2−アセチルー4.4
−ジメチル−3−ピ5ゾ)ドン,1−p−ヒドロキシフ
エニルー4.4−ジメチル−3−ビラゾリドン、1−(
2一ベンゾチアゾリル)−3−ビラゾリドン、3一ア七
Fキシ−1−フエニルー3−ビラゾリドン)等を単独も
しくは組合せて含有したアルカリ水浴液であることが灯
ましい。The developer processing solution of this invention is a conventional developing agent for black and white photography, such as hydroquinone, alkylnohydroquinone (e.g. t-butylnohydroquinone, methylhydroquinone,
dimethylhydroquinone), catechol, pyrazole, chlorohydroquinone, dichlorohydroquinone, alkoxynohydroquinone (e.g. methoxy or ethoxynohydroquinone), aminone enol developing crude drugs (e.g. N-methyl-p-aminoneenol, 2,4-diaminophenol), Ascorbic acid developer bath, N-methyl-p-aminophenol sulfate, virazolones (e.g. 4-aminovirazolone), 3-virazolidone developing agents (e.g. 1-7enyl-3-virazolidone, 1-
Phenyl-4,4-dimethyl-3-birasolidone, 1-
7enyl-5-methyl-3-hira7” IJ don,
1-7enyl-4-methyl-3-virazolidone, 1.5
-di7enyl-3-virazolidone, 1-p-}lilu 3
-Vyrazolidone, 1-phenyl-2-acetyl 4.4
-dimethyl-3-pi5zo)done, 1-p-hydroxyphenyl-4,4-dimethyl-3-virazolidone, 1-(
Preferably, it is an alkaline water bath solution containing 2-benzothiazolyl)-3-virazolidone, 31-a7Fx-1-phenyl-3-virazolidone), etc. alone or in combination.
特にハイドロキノンと3−ビラゾリドン類あるいはハイ
ドロキノンとアミノフェノール類との組合せが烏温迅速
な処理には有用である。In particular, a combination of hydroquinone and 3-virazolidones or a combination of hydroquinone and aminophenols is useful for rapid treatment at Ooto.
但し、現像主薬を実質的に含有しない、所f.’fJア
クチペータタイプの現像液であってもよい。However, f. which does not substantially contain a developing agent. 'fJ actipator type developer may be used.
本発明に用いられる一般式〔1〕で表わされる化合物を
含有した現像液は、多菫の亜硫酸イオン金含有している
ときに、スラツジ防止効果を特VC顕著に発揮する。こ
のとき具体的には、現像液1t当り0.1モル以上、好
筐し〈は0.2モルから1.0モルの亜硫酸イオンを含
有している。亜硫酸イオンを与える亜硫酸塩としては、
具体的には亜硫酸塩ナトリウム、亜硫酸カリウム、メタ
重亜硫酸カリウムなどのアルカリ金属の亜硫酸塩を用い
ることができる。The developer containing the compound represented by the general formula [1] used in the present invention exhibits a remarkable sludge-preventing effect especially when it contains polysulfite ion gold. At this time, specifically, the developing solution contains 0.1 mol or more, preferably 0.2 mol to 1.0 mol, of sulfite ions per ton of developer. As a sulfite that gives sulfite ions,
Specifically, alkali metal sulfites such as sodium sulfite, potassium sulfite, and potassium metabisulfite can be used.
現像液中に発生する銭スラツジは、%に現像機中のロー
ラーやベルトに沈着しやすく、しかもローラーやベルト
に付着した銀スラツジは感光材料を汁染しやすい。した
がって本晃IJI]は自動現保樋で処理する場合K特に
有効に用いられる。The silver sludge generated in the developer tends to deposit on the rollers and belts in the developing machine, and the silver sludge that adheres to the rollers and belts tends to stain the photosensitive material. Therefore, this method is particularly effective when processing with an automatic maintenance gutter.
かかる自動現像機としては、例えば対向ローラ一方式(
例えばPA.KO社Pakorol Super 02
4−2、富士写真フイルム社G−14L%PG−24
SQ,RNなど)、千鳥ローラ一方式(例えばEast
man Kodak社Kodalith Proces
sor, M6 Processor, g±写真フ
イルム社RUなと)、ベルト搬送方式(例えばLog−
E − tronics社LD−241Dなど)そ0)
Ilb ( d upon t社Cronalith
24Lなど)たごがある。As such an automatic developing machine, for example, a one-type facing roller type (
For example, P.A. KO company Pakorol Super 02
4-2, Fuji Photo Film Co., Ltd. G-14L%PG-24
SQ, RN, etc.), staggered roller one type (e.g. East
man Kodak Kodalith Processes
sor, M6 Processor, g±Photo Film Co., Ltd. RU), belt conveyance method (e.g. Log-
E-tronics LD-241D etc.) 0)
Ilb (dupont company coronalith
24L, etc.) There is an egg.
現像液には、その他必証により緩衝剤(例えば、炭酸塩
、硼酸、硼酸塩、アルカノールアミン)、アルカリ剤(
例えば、水酸化物、炭酸塩)、溶跡助剤(例えば、ポリ
エチレングリコール類、これらのエステル)、p}1調
整剤(例えば、酢酸の如き有機酸)、増感剤(例えば、
四級アンモニウム塩)、現像促進剤、界曲活性剤、硬脱
剤などを罰有させることができる。The developer may contain other buffering agents (e.g., carbonates, boric acid, borates, alkanolamines), alkaline agents (
(e.g. hydroxides, carbonates), solvent aids (e.g. polyethylene glycols, esters thereof), p}1 regulators (e.g. organic acids such as acetic acid), sensitizers (e.g.
Quaternary ammonium salts), development accelerators, interfacial activators, hardening agents, etc. can be added.
現像液には更に、カブリ防止剤(例えは、5一二トロイ
ンダゾール、5−ニトローペンツイミダゾール、5−メ
チルーベンゾトリアゾール、5一二トロベンゾトリアゾ
ールの如きペンゾトリアゾール、ペンゾチアゾール、l
−7エニルー5−メルカブトーテトラゾールの如きテト
ラゾール、チアゾール或いは英国W許1t,2ac+,
2ss号に記載の化合物など)、キレート化剤(例えは
、エチレンジアミン四酢酸、これらのアルカリ金域塩、
ポリリン酸塩、ニトリロ酢酸塩)f:含有させることが
できる。The developer further contains antifoggants (for example, penzotriazoles such as 5-1 ditroindazole, 5-nitropenzimidazole, 5-methyl-benzotriazole, 5-1 ditrobenzotriazole, penzothiazole, l).
Tetrazole such as -7enyl-5-mercabutotetetrazole, thiazole or British W license 1t, 2ac+,
2ss), chelating agents (e.g., ethylenediaminetetraacetic acid, alkali metal salts thereof,
Polyphosphate, nitriloacetate) f: Can be contained.
この様にしてルM整された現像液のp■値は所望の濃度
とコントラストヲ与えるに充分な程度に選択されるが、
約8〜12の範囲にあることが望lしい。The p value of the developer prepared in this way is selected to be sufficient to provide the desired density and contrast.
Desirably, it is in the range of about 8-12.
現像処理温度及び時間は相互に関係し、且つ全処理時間
との関係において決定され、一般に約20〜50℃で1
0秒〜3分であるが、高温迅速処理の場合には約30〜
60℃の温度である。Processing temperature and time are interrelated and determined in relation to the total processing time, generally at about 20-50°C.
0 seconds to 3 minutes, but in the case of high temperature rapid processing, it takes about 30 seconds to 3 minutes.
The temperature is 60°C.
本発明に於では、現像液のかかる成分は、使用時に必要
な成分が含有されてかれはよく、使用に際して使用液と
して調合する前の処理前の形態は例えば固体成分の混合
物、濃厚物、溶液、エマルジョンまたは懸濁物など如何
なるものでもよい。In the present invention, the components of the developing solution may contain any necessary components at the time of use, and the form before processing before preparing the working solution for use may be, for example, a mixture of solid components, a concentrate, or a solution. , emulsion or suspension.
例えば、現像液の戒分をいくつかの部分に分けて同一の
形態又は異った形態にされた現像液でもよ〈、これらを
予め調合した粉状又は液状の調合液の形態であってもよ
い。For example, it may be a developer that is divided into several parts and made into the same form or different forms. good.
調合剤は使用に際して必要により、水に溶解又は水で希
釈して使用液とすることが出来る。The preparation can be dissolved in water or diluted with water to prepare a working solution, if necessary.
他方、定着液はチオ硫酸塩、水浴性アルミニウム化合物
を含む水溶液であり、望ましくはpH約3.8〜5.5
(20℃)を有する。本発明の方法において、現像の後
に停止工程を設けることもできるが、一般にローラー搬
送型の自動現像機には停止工程が省略されている。その
ために現像液が定着液K持ち込まれ、定着液のpHが上
昇する。そのために、定N族のpHは約3.8〜5.0
(20℃)に洲整してシ〈ことが望ましい。On the other hand, the fixing solution is an aqueous solution containing thiosulfate and a water-bathable aluminum compound, and preferably has a pH of about 3.8 to 5.5.
(20°C). In the method of the present invention, a stopping step may be provided after development, but the stopping step is generally omitted in roller conveyance type automatic developing machines. Therefore, the developer is brought into the fixer K, and the pH of the fixer increases. Therefore, the pH of the constant N group is about 3.8 to 5.0.
It is desirable to adjust the temperature to (20°C).
定着剤はチオ硫酸アンモニウム、チオ硫酸ナトリウムな
どのチオ硫酸塩であり、定着速度の点からチオ硫酸アン
モニウムが特に灯1しい。定着剤の使用量は適宜変える
ことができ、一般には約0.1〜5モル/tである〇
定着液中で主として硬膜剤として作用する水溶性アルミ
ニウム塩は一般に酸性硬膜定着液の硬膜剤として知られ
ている化合物であり、例えば塩化アルミニウム、硫酸ア
ルミニウム、カリ明ばんなどがある。The fixing agent is a thiosulfate salt such as ammonium thiosulfate or sodium thiosulfate, and ammonium thiosulfate is particularly preferred from the viewpoint of fixing speed. The amount of the fixing agent used can be changed as appropriate, and is generally about 0.1 to 5 mol/t. Water-soluble aluminum salt, which mainly acts as a hardening agent in the fixing solution, generally improves the hardness of the acidic hardening fixer. It is a compound known as a film agent, such as aluminum chloride, aluminum sulfate, and potassium alum.
本発明の方法によれば、現像、定着された写真材料は水
洗及び乾燥される。水洗は定着によって溶解した銀塩を
ほぼ完全に除くために行なわれ、約5〜50℃で10秒
〜3分が好筐しい。乾燥は約30〜80℃で行なわれ、
乾燥時間は周囲の状態によって適宜変えられるが、通常
は約5秒〜3分30秒でよい。According to the method of the invention, the developed and fixed photographic material is washed and dried. Washing with water is carried out to almost completely remove the silver salt dissolved during fixing, and is preferably carried out at about 5 to 50° C. for 10 seconds to 3 minutes. Drying is carried out at approximately 30-80°C,
Although the drying time can be changed as appropriate depending on the surrounding conditions, it is usually about 5 seconds to 3 minutes and 30 seconds.
本発明の方法によって処理される感光材料はいかたる用
途のものであっても差し支えないが、好筐しくは、白黒
用感材すなわち,Xレイ感材、マィクロ感材、アンリス
用感材、写植用感材、一般アマチア用白黒感材などに適
用される。感光層のハロゲン化銀は塩化銀、塩兵化銀、
塩沃臭化銀、英化銀,沃臭化銀などである。1た本発明
に使用する感光材料はネガ型又は直接ポジ型いずれであ
ってもよい。The photosensitive material processed by the method of the present invention may be used for any purpose, but preferably black and white photosensitive materials, such as X-ray photosensitive materials, micro photosensitive materials, Anrith photosensitive materials, and phototypesetting photosensitive materials. Applicable to photosensitive materials, general amateur black and white photosensitive materials, etc. The silver halide in the photosensitive layer is silver chloride, silver chloride,
These include silver chloroiodobromide, silver oxide, and silver iodobromide. The photosensitive material used in the present invention may be of either negative type or direct positive type.
本発明の方法に適用できるハロゲン化銀写真感光材料は
支持体とその上に塗布された少なくとも一つのハロゲン
化銀乳剤層からなる。また、ハロゲン化銀乳剤層は支持
体の片面だけでなく両面に塗而されることもできる。も
ちろん,必要によりパック層、アンチハレーション層、
中間層、最上層(例えば、保護層〕たごを有することが
できる。A silver halide photographic material applicable to the method of the present invention comprises a support and at least one silver halide emulsion layer coated thereon. Further, the silver halide emulsion layer can be coated not only on one side of the support but also on both sides. Of course, if necessary, pack layer, anti-halation layer, etc.
It can have an intermediate layer and a top layer (eg, a protective layer).
ハロゲン化銀乳剤はハロゲン化銀を親水性コロイド(例
えば、ゼラチン、変性ゼラチン,コロイト状アルプミン
、カゼイン、カルボキシメチルセルロース、ヒドロキシ
エチルセルロース、アルギン酸ンーダ、ポリビニルアル
コール、ポリビニルビロリドン又はこれらの混合物など
)に分散したものである。ハロゲン化銀乳剤は、通常当
業界でよ?知られた方法(例えば、シングルジェット法
、ダブルジェット法、コントロールジェット法など)に
工って水溶性銀塩(例えば、硝酸銀)と水浴性ハロゲン
塩とを水及び親水性コロイドの存在下で混合し、物理熟
成及び金増感及び/又は硫黄増感たどの化学熟成を経て
製造される。ハロゲン化銀乳剤には、その製造工程中又
は塗布直前で、分光増感剤(例えば、シアニン色素、メ
ロシアニン色素又はその混合物)、安定剤(例えば、4
−ヒドロキシ−6−メチル−1. 3. 3a, 7−
テトラザインデン)、増感剤(例えば、米国特許第3,
619,198号明細書に記載の化合物)、カプリ防止
剤(例,t}f,ペン/− } IJアゾール、5−ニ
トロベンツイ■ダゾール、ポリエチレンオキサイド)、
硬膜剤(例えば、ホルマリン、グリオキザール、ムコク
ロル酸、2−ヒドロキシ−4.6−ジクロローS−トリ
アジン)、塗布助剤(例えば、サボニン、ソジウムラウ
リルサルフエート、ドデシルフェノールポリエチレンオ
キサイドエーテル、ヘキサデシルトリメチルアンモニウ
ムブロマイド)などを添加することができる。この様に
して製造されたハロゲン化銀乳剤はパライタ紙、レジン
コーテッド紙、セルロースアセテートフィルム、ポリエ
チレンテレフタレートフイルムなどの支持体にデイフプ
法、エアーナイフ法、ピード法,エクストルージョンド
クター法、両面塗父法などによって塗イ[乾燥される。Silver halide emulsions are silver halide emulsions dispersed in hydrophilic colloids such as gelatin, modified gelatin, colloidal albumin, casein, carboxymethylcellulose, hydroxyethylcellulose, alginate, polyvinyl alcohol, polyvinylpyrrolidone, or mixtures thereof. This is what I did. Silver halide emulsions are commonly used in the industry. A water-soluble silver salt (e.g., silver nitrate) and a bathable halide are mixed in the presence of water and a hydrophilic colloid using known methods (e.g., single-jet method, double-jet method, controlled-jet method, etc.). It is produced through physical ripening and chemical ripening such as gold sensitization and/or sulfur sensitization. Silver halide emulsions may contain spectral sensitizers (e.g. cyanine dyes, merocyanine dyes or mixtures thereof), stabilizers (e.g.
-Hydroxy-6-methyl-1. 3. 3a, 7-
tetrazaindene), sensitizers (e.g., U.S. Pat.
619,198), anti-capri agents (e.g., t}f, pen/-} IJ azole, 5-nitrobenzydazole, polyethylene oxide),
Hardeners (e.g. formalin, glyoxal, mucochloric acid, 2-hydroxy-4,6-dichloro-S-triazine), coating aids (e.g. sabonin, sodium lauryl sulfate, dodecylphenol polyethylene oxide ether, hexadecyl trimethyl Ammonium bromide) etc. can be added. The silver halide emulsion produced in this manner is coated on a support such as Paraita paper, resin-coated paper, cellulose acetate film, or polyethylene terephthalate film using the dihupping method, air knife method, pead method, extrusion doctor method, double-sided coating method, etc. It is coated [dry] by etc.
(実施例)
次に、本発明を実施例を挙げて詳細に説明するが勿論こ
れらに限定されるものではない。(Example) Next, the present invention will be explained in detail by giving examples, but of course it is not limited to these.
実施例1
下記の現像液(A)〜(F)を調製した。いずれもpH
10.65であった。Example 1 The following developing solutions (A) to (F) were prepared. Both pH
It was 10.65.
現像戚(A)
現像}夜(B)
現像液(A)に例示化合物(1)k500η添加したも
の。Development (A) Development (B) Exemplary compound (1) k500η was added to developer (A).
現像液(C)
現像液(A)に例示化合物(2) ′jt500η添加
したもの。Developer (C) Exemplified compound (2) was added to developer (A) in an amount of 500η.
現像液CD)
現像液(A)に例示化合物(6)を500η添加したも
の。Developer solution CD) 500η of exemplified compound (6) was added to developer (A).
現イ象゛63ξ(E)
比較化合物として、一般式〔I〕でA=8H,B=N
H C 6H 5の化合物fr.500η添加したもの
。Phenomenon ゛63ξ(E) As a comparative compound, in the general formula [I], A=8H, B=N
H C 6H 5 compound fr. Added 500η.
現像i (F)
比較化合物として、一般式〔I〕でA=SH,B=N(
C2H5)2の化合物を5009添加したもの。Development i (F) As a comparative compound, A=SH, B=N(
Added 5009 of C2H5)2 compound.
1た、定着液としては下記のものを用いた。1. The following fixer was used.
チオ硫酸アンモニウム 200.Of亜硫酸ナ
トリウム(無水) 20.O r硼酸
8.02
エチレンジアミン四酢酸二ナトリウム 0.12
硫酸アルミニウム 15.Of硫酸
2,of
氷酢酸 22.of水を加えて
1.Ot(p}1は4.2に
調整する)
次に、このようにして調製した現像液(A)〜(F)に
ついてそれぞれ以下の実験を行なった。Ammonium thiosulfate 200. Of Sodium Sulfite (Anhydrous) 20. Boric acid
8.02 Ethylenediaminetetraacetic acid disodium 0.12
Aluminum sulfate 15. Ofsulfuric acid
2, of glacial acetic acid 22. Add water 1. Ot(p}1 is adjusted to 4.2) Next, the following experiments were conducted on the developers (A) to (F) prepared in this manner.
現13!液221をローラ搬送型の自動現像機中に入れ
、ポリエチレンテレフタレート上に塩臭化銀(塩化銀5
0モル%)乳剤層金有する黒白写真フ゛イルム(@量4
、51/n?)f画像露光したのち上記現像機に送入し
て現像した。な訃現保温度は38℃、現像時間は20秒
で行ない、大全紙サイズ(20インチ×24インチ)1
枚現像するごとに現像液を100−の割合で自動的に補
充した。Currently 13! Liquid 221 was put into a roller conveyance type automatic developing machine, and silver chlorobromide (silver chloride 5
0 mol%) black and white photographic film with emulsion layer gold (@ amount 4
, 51/n? ) After exposing the f image, it was fed into the above-mentioned developing machine and developed. The development temperature was 38℃, the development time was 20 seconds, and the large paper size (20 inches x 24 inches) 1
Each time a sheet was developed, the developer was automatically replenished at a rate of 100.
1日に大全紙サイズのフイルム100枚を5時間にわた
って現像、この処理操作を1週間続けてあ・こなった。I developed 100 sheets of paper-sized film in one day for five hours, and continued this process for a week.
本発明の一般式CDの化合物を加えてない現像i(A液
)では、最初のフイルム100枚を現像している間に、
最初無色透明であった現像液がすぐにとり始め、銀スラ
ツジの沈積が認められるようになった。In developing i (liquid A) to which the compound of the general formula CD of the present invention is not added, while developing the first 100 films,
The developing solution, which was initially colorless and transparent, soon began to dissolve, and deposits of silver sludge began to be observed.
フイルムにはしま状の銀汚れが生じ始めた。1週間の処
理中にこの汚れは1す甘すひど〈t[つた。Striped silver stains began to appear on the film. During the one-week treatment, this stain became very bad.
現像液中にはひどい濁りと銀スラッジの沈積があり、自
動現像機のローラーにもひどい銀汚れがあった。フイル
ムにもし1状の銀汚れが処理教数が増えるにしたがって
ひどくなっていった。There was severe turbidity and silver sludge deposits in the developer, and there was also severe silver staining on the rollers of the automatic processor. The silver stains on the film became more severe as the number of treatments increased.
筐たフイルムの表面にはローラーに付着したスラツジへ
の接触によって生じたと思われる損傷も認められた。Damage that appeared to have been caused by contact with the sludge adhering to the rollers was also observed on the surface of the encased film.
1た比較化合物金加えた現像液〔E〕及び〔F〕では、
1週間の現像処理でも銀スラツジは殆んど認められなか
ったが、現像液の調製直後から、現像液[A]での写X
特性に比べて激しい減感軟調化、最高濃度の低下があっ
た。In developer solutions [E] and [F] containing comparative compound gold,
Almost no silver sludge was observed even after one week of development, but immediately after the developer was prepared,
Compared to the characteristics, there was severe desensitization and softening, and a decrease in the maximum density.
一方、本発明に係る化合物を加えた現像液[B)、〔C
〕及び[D]では、1週間の現像処理でも銀スラツジは
全く認められず、透明性を維持していた。On the other hand, developing solutions [B] and [C
] and [D], no silver sludge was observed even after one week of development, and transparency was maintained.
更に現像液〔A〕での写真特性と比べても何ら劣るとこ
ろは無く、良好な写真特性を有していた。Furthermore, when compared with the photographic properties using developer [A], there was no inferiority in the photographic properties, and the photographic properties were good.
実施例2 下記の現像液CP) ’k調製した。Example 2 The following developer solution CP) was prepared.
現像液〔P〕
現像液〔P〕に例示化合物(1)〜(10)を各々30
0my添加した10種類の現像液。Developer [P] Add 30% each of Exemplified Compounds (1) to (10) to Developer [P].
10 types of developer with 0my added.
ポリエチレンテレフタレート上に塩化銀乳剤層を有する
黒白写真フイルム(銀i3.!M/m”)を用いる以外
は実施例1の条件に準じて試験した。A test was conducted according to the conditions of Example 1, except that a black and white photographic film (silver i3.!M/m'') having a silver chloride emulsion layer on polyethylene terephthalate was used.
現像液[Plは,著しい銀スラツジが発生したが、現像
液〔Q〕〜〔Z〕はいずれも銀スラッジの発生が認めら
れず、写真特性も伺ら異常なかった。Although significant silver sludge was generated in the developer [Pl], no silver sludge was observed in any of the developers [Q] to [Z], and the photographic properties showed no abnormality.
(発明の効果)
本発明は、亜硫酸塩のようなハロゲン化銀の溶剤を含む
現像液で生じる銀スラッジを、一般式〔I〕のメルヵブ
}fヒ合物を使用することにより、写真特性′li−損
なうことなく極めて良妊に防止できる。(Effects of the Invention) The present invention improves the photographic properties of silver sludge produced in a developer containing a silver halide solvent such as sulfite by using a mercab compound of the general formula [I]. li - can prevent very good fertility without causing any damage.
Claims (1)
ことを特徴とするハロゲン化銀写真感光材料用現像液。 一般式〔 I 〕 ▲数式、化学式、表等があります▼ (式中、A及びBは、メルカプト基、ヒドロキシル基、
ヒドロキシアルキル基、▲数式、化学式、表等がありま
す▼基を表わす。R_1及びR_2は、水素原子、−X
−Y基を表わし、Xは2価基、Yはカルボキシル基、ヒ
ドロキシル基を表わす。)[Scope of Claims] 1. A developer for silver halide photographic materials, which contains a compound represented by the following general formula [I]. General formula [I] ▲There are mathematical formulas, chemical formulas, tables, etc.▼ (In the formula, A and B are mercapto group, hydroxyl group,
Represents a hydroxyalkyl group, ▲ mathematical formula, chemical formula, table, etc. ▼ group. R_1 and R_2 are hydrogen atoms, -X
-Y group, where X is a divalent group and Y is a carboxyl group or a hydroxyl group. )
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18626589A JPH0623830B2 (en) | 1989-07-21 | 1989-07-21 | Developer for silver halide photographic materials |
DE19904023143 DE4023143C2 (en) | 1989-07-21 | 1990-07-20 | Developer for a silver halide photographic light-sensitive material |
US08/020,458 US5300410A (en) | 1989-07-21 | 1993-02-22 | Developer for silver halide photographic light-sensitive material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18626589A JPH0623830B2 (en) | 1989-07-21 | 1989-07-21 | Developer for silver halide photographic materials |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0353244A true JPH0353244A (en) | 1991-03-07 |
JPH0623830B2 JPH0623830B2 (en) | 1994-03-30 |
Family
ID=16185260
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18626589A Expired - Fee Related JPH0623830B2 (en) | 1989-07-21 | 1989-07-21 | Developer for silver halide photographic materials |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0623830B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04362942A (en) * | 1991-04-02 | 1992-12-15 | Fuji Photo Film Co Ltd | Method for development of silver halide photographic sensitive material and its developer |
JPH05303179A (en) * | 1991-04-18 | 1993-11-16 | Fuji Photo Film Co Ltd | Developing method for silver halide photographic sensitive material and developer composition |
EP0789272A1 (en) | 1996-02-07 | 1997-08-13 | Fuji Photo Film Co., Ltd. | Developer for silver halide photographic photosensitive material |
JP2017048159A (en) * | 2015-09-04 | 2017-03-09 | 四国化成工業株式会社 | Triazine compound, method for the synthesis of the compound and use therefor |
-
1989
- 1989-07-21 JP JP18626589A patent/JPH0623830B2/en not_active Expired - Fee Related
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04362942A (en) * | 1991-04-02 | 1992-12-15 | Fuji Photo Film Co Ltd | Method for development of silver halide photographic sensitive material and its developer |
JPH05303179A (en) * | 1991-04-18 | 1993-11-16 | Fuji Photo Film Co Ltd | Developing method for silver halide photographic sensitive material and developer composition |
EP0789272A1 (en) | 1996-02-07 | 1997-08-13 | Fuji Photo Film Co., Ltd. | Developer for silver halide photographic photosensitive material |
US5840472A (en) * | 1996-02-07 | 1998-11-24 | Fuji Photo Film Co., Ltd. | Developer for silver halide photographic photosensitive material |
JP2017048159A (en) * | 2015-09-04 | 2017-03-09 | 四国化成工業株式会社 | Triazine compound, method for the synthesis of the compound and use therefor |
Also Published As
Publication number | Publication date |
---|---|
JPH0623830B2 (en) | 1994-03-30 |
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