EP0136582A2 - Developer compositions for silver halide photographic materials - Google Patents
Developer compositions for silver halide photographic materials Download PDFInfo
- Publication number
- EP0136582A2 EP0136582A2 EP84110559A EP84110559A EP0136582A2 EP 0136582 A2 EP0136582 A2 EP 0136582A2 EP 84110559 A EP84110559 A EP 84110559A EP 84110559 A EP84110559 A EP 84110559A EP 0136582 A2 EP0136582 A2 EP 0136582A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- acid
- grams per
- per liter
- amount
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 66
- -1 silver halide Chemical class 0.000 title claims abstract description 43
- 229910052709 silver Inorganic materials 0.000 title claims abstract description 28
- 239000004332 silver Substances 0.000 title claims abstract description 28
- 239000000463 material Substances 0.000 title claims abstract description 22
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 49
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims abstract description 38
- 239000002253 acid Substances 0.000 claims abstract description 16
- 239000003352 sequestering agent Substances 0.000 claims abstract description 16
- 239000003513 alkali Substances 0.000 claims abstract description 13
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 13
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 claims abstract description 11
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 30
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 27
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 18
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 17
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 14
- 239000012964 benzotriazole Substances 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- GGZHVNZHFYCSEV-UHFFFAOYSA-N 1-Phenyl-5-mercaptotetrazole Chemical compound SC1=NN=NN1C1=CC=CC=C1 GGZHVNZHFYCSEV-UHFFFAOYSA-N 0.000 claims description 12
- 235000011054 acetic acid Nutrition 0.000 claims description 10
- 229920000388 Polyphosphate Polymers 0.000 claims description 9
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 9
- 235000015165 citric acid Nutrition 0.000 claims description 9
- 239000004310 lactic acid Substances 0.000 claims description 9
- 235000014655 lactic acid Nutrition 0.000 claims description 9
- 235000011007 phosphoric acid Nutrition 0.000 claims description 9
- 239000001205 polyphosphate Substances 0.000 claims description 9
- 235000011176 polyphosphates Nutrition 0.000 claims description 9
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 8
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 7
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 claims description 7
- WSGURAYTCUVDQL-UHFFFAOYSA-N 5-nitro-1h-indazole Chemical compound [O-][N+](=O)C1=CC=C2NN=CC2=C1 WSGURAYTCUVDQL-UHFFFAOYSA-N 0.000 claims description 6
- AOCDQWRMYHJTMY-UHFFFAOYSA-N 5-nitro-2h-benzotriazole Chemical compound C1=C([N+](=O)[O-])C=CC2=NNN=C21 AOCDQWRMYHJTMY-UHFFFAOYSA-N 0.000 claims description 6
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical class O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 claims description 6
- NSYCNXOFRPQHGG-UHFFFAOYSA-N 1h-benzimidazole;nitric acid Chemical compound O[N+]([O-])=O.C1=CC=C2NC=NC2=C1 NSYCNXOFRPQHGG-UHFFFAOYSA-N 0.000 claims description 5
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 5
- XNIOWJUQPMKCIJ-UHFFFAOYSA-N 2-(benzylamino)ethanol Chemical compound OCCNCC1=CC=CC=C1 XNIOWJUQPMKCIJ-UHFFFAOYSA-N 0.000 claims description 4
- MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-UHFFFAOYSA-N 0.000 claims description 3
- RILLZYSZSDGYGV-UHFFFAOYSA-N 2-(propan-2-ylamino)ethanol Chemical compound CC(C)NCCO RILLZYSZSDGYGV-UHFFFAOYSA-N 0.000 claims description 3
- DPRMFUAMSRXGDE-UHFFFAOYSA-N ac1o530g Chemical compound NCCN.NCCN DPRMFUAMSRXGDE-UHFFFAOYSA-N 0.000 claims 1
- 230000003647 oxidation Effects 0.000 abstract description 11
- 238000007254 oxidation reaction Methods 0.000 abstract description 11
- 229910021645 metal ion Inorganic materials 0.000 abstract description 6
- 239000000470 constituent Substances 0.000 abstract description 2
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 28
- 238000009472 formulation Methods 0.000 description 10
- WYMDDFRYORANCC-UHFFFAOYSA-N 2-[[3-[bis(carboxymethyl)amino]-2-hydroxypropyl]-(carboxymethyl)amino]acetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)CN(CC(O)=O)CC(O)=O WYMDDFRYORANCC-UHFFFAOYSA-N 0.000 description 7
- 239000007788 liquid Substances 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 3
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-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
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- YDONNITUKPKTIG-UHFFFAOYSA-N [Nitrilotris(methylene)]trisphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CP(O)(O)=O YDONNITUKPKTIG-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 2
- CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 2
- 229910019931 (NH4)2Fe(SO4)2 Inorganic materials 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-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
- XGIKILRODBEJIL-UHFFFAOYSA-N 1-(ethylamino)ethanol Chemical compound CCNC(C)O XGIKILRODBEJIL-UHFFFAOYSA-N 0.000 description 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-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
- UBXZEGXUHNQQOF-UHFFFAOYSA-N 2-(2-aminoethyl)-2-(hydroxymethyl)propane-1,3-diol Chemical compound NCCC(CO)(CO)CO UBXZEGXUHNQQOF-UHFFFAOYSA-N 0.000 description 1
- UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 description 1
- REFDOIWRJDGBHY-UHFFFAOYSA-N 2-bromobenzene-1,4-diol Chemical compound OC1=CC=C(O)C(Br)=C1 REFDOIWRJDGBHY-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
- 239000001763 2-hydroxyethyl(trimethyl)azanium Substances 0.000 description 1
- PYSGFFTXMUWEOT-UHFFFAOYSA-N 3-(dimethylamino)propan-1-ol Chemical compound CN(C)CCCO PYSGFFTXMUWEOT-UHFFFAOYSA-N 0.000 description 1
- ZZEYCGJAYIHIAZ-UHFFFAOYSA-N 4-methyl-1-phenylpyrazolidin-3-one Chemical compound N1C(=O)C(C)CN1C1=CC=CC=C1 ZZEYCGJAYIHIAZ-UHFFFAOYSA-N 0.000 description 1
- 235000019743 Choline chloride Nutrition 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-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
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
- LXMPJPJANHMZCZ-UHFFFAOYSA-N SC1=CN=NN1C1=CC=CC=C1 Chemical compound SC1=CN=NN1C1=CC=CC=C1 LXMPJPJANHMZCZ-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- XIWMTQIUUWJNRP-UHFFFAOYSA-N amidol Chemical compound NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 150000001556 benzimidazoles Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- AJPXTSMULZANCB-UHFFFAOYSA-N chlorohydroquinone Chemical compound OC1=CC=C(O)C(Cl)=C1 AJPXTSMULZANCB-UHFFFAOYSA-N 0.000 description 1
- SGMZJAMFUVOLNK-UHFFFAOYSA-M choline chloride Chemical compound [Cl-].C[N+](C)(C)CCO SGMZJAMFUVOLNK-UHFFFAOYSA-M 0.000 description 1
- 229960003178 choline chloride Drugs 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
- BXJGUBZTZWCMEX-UHFFFAOYSA-N dimethylhydroquinone Natural products CC1=C(C)C(O)=CC=C1O BXJGUBZTZWCMEX-UHFFFAOYSA-N 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 229960002449 glycine Drugs 0.000 description 1
- 235000013905 glycine and its sodium salt Nutrition 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
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 159000000014 iron salts Chemical class 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- PCILLCXFKWDRMK-UHFFFAOYSA-N naphthalene-1,4-diol Chemical compound C1=CC=C2C(O)=CC=C(O)C2=C1 PCILLCXFKWDRMK-UHFFFAOYSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 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
- 238000002360 preparation method Methods 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000000837 restrainer Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229940001584 sodium metabisulfite Drugs 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000012224 working solution 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
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/29—Development processes or agents therefor
- G03C5/305—Additives other than developers
- G03C5/3053—Tensio-active agents or sequestering agents, e.g. water-softening or wetting agents
Definitions
- the present invention relates to a developer composition for silver halide photographic materials comprising:
- the single part concentrated developer composition above comprises an auxiliary developing agent selected from the class of substituted pyrazolidone and para-aminophenol compounds.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Abstract
Description
- The present invention relates to developer compositions for silver halide photographic materials and, particularly, to photographic silver halide developer compositions having improved resistance to aerial oxidation.
- In general, treatment of black and white silver halide photographic materials is carried out in the order of development, stopping, fixing and washing.
- Development is ordinarily carried out with alkaline developers containing hydroquinone as a developing agent and alkali metal sulfite as a preservative. Such developers tend to be oxidized by the air during preparation, working and storage. It is a well-known phenomenon that traces of certain metal ions, such as copper and iron, have a catalytic effect on the aerial oxidation of developers (the metal ions may have been introduced as an impurity into the water or into the chemicals used to compound the developing solution).
- Some compounds have been proposed to reduce or eliminate the catalytic effect of such metal ions, especially iron, on the aerial oxidation of developers by forming very stable complexes with said metal ions in alkaline solution, but their activity is reduced to a high degree when silver halide photographic materials are treated in continuous transport processing machines, especially at high temperatures. In that case, considerable quantities of air are introduced into developer solutions used in processing machines, this aeration oxidizing more of the developing agent than the real development process itself, causing a rapid degradation of the developer.
- A developer composition for silver halide photographic materials has been found which has improved resistance to air oxidation, even in the presence of metal ion traces. The composition can be left in continuous transport processing machines for several days, said developer compositions having the following constituents:
- (a) hydroquinone or a substituted hydroquinone,
- (b) an auxiliary superadditive developing agent,
- (c) an alkali metal sulfite,
- (d) an organic-antifoggant agent,
- (e) inorganic alkali agents,
- (f) an alkanolamine, and
- (g) a sequestering agent selected in the group of diethylenetetraminepentacetic acid (hereinafter referred to as DTPA), 1,3-diamino-2-propanoltetracetic acid (hereinafter referred to as DTPA) and 1-hydroxyethylidene-1,1'-diphosphonic acid (hereinafetr referred to as HEDP).
- The present invention relates to a developer composition for silver halide photographic materials comprising hydroquinone or a substituted hydroquinone, an alkali metal sulfite, an organic antifoggant agent and inorganic alkali agents, characterized by further comprising an alkanolamine and a sequestering agent selected in the group of DTPA, DPTA and HEDP.
- Preferably, the above described developer composition comprises an additional compound selected in the group of polyphosphates, phosphoric acid, acetic acid, lactic acid and citric acid.
- More preferably, the developer composition above comprises an auxiliary developing agent selected from the class of substituted pyrazolidone and p-aminophenol compounds.
- Still more preferably, the organic antifoggant agent is selected from the group of mixtures of 5-nitroindazole and benzimidazole nitrate, 5-nitrobenzotriazole and 1-phenyl-5-mercaptotetrazole, and benzotriazole and 1-phenyl-5-mercaptotetrazole and/or the alkanolamine is selected from the group of diethanolamine, triethanolamine, 2-benzylaminoethanol, 2-methylaminoethanol, 2-ethylaminoethanol and 2-isopropyl- aminoethanol.
- In particular the present invention relates to a developer composition for silver halide photographic materials comprising:
- (a) hydroquinone or a substituted hydroquinone in an amount from about 5 to 50, preferably 10 to 30 grams per liter;
- (b) an auxiliary developing agent in an amount from about 0.1 to 15, preferably 0.2 to 5 grams per liter;
- (c) an alkali metal sulfite in an amount from about 15 to 100, preferably 20 to 50 grams per liter;
- (d) an alkanolamine in an amount from about 10 to 30, preferably 5 to 20 grams per liter;
- (e) an organic antifoggant agent selected in the group of mixtures of 5-nitroindazole and benzimidazole nitrate, 5-nitrobenzotriazole and 1-phenyl-5-mercaptotetrazole, and benzotriazole and 1-phenyl-5-mercaptotetrazole, in an amount from about 0.1 to 3, preferably 0.2 to 1.5 grams per liter;
- (f) a sequestering agent selected from the group of DTPA, DPTA and HEDP in an amount from about 5 to 50, preferably 10 to 30 grams per liter;
- (g) a compound selected in the group of polyphosphates, phosphoric acid, acetic acid, lactic acid and citric acid in an amount from about 5 to 100, preferably 15 to 50 grams per liter;
- (h) inorganic alkali agents sufficient to provide a pH of at least 10 and
- (i) water sufficient to make up 1 liter.
- In another aspect the present invention relates to a single part concentrated developer composition for silver halide photographic materials, to be diluted with water and form a ready for use developer solution, comprising hydroquinone or a substituted hydroquinone, an alkali metal sulfite and inorganic alkali agents, characterized in that it contains an alkanolamine, an organic sequestering agent selected in the group of DTPA, DPTA and HEDP and a mixture of benzotriazole and 1-phenyl-5- mercaptotetrazole antifogging agents.
- Preferably, the single part concentrated developer composition above further comprises a compound selected in the group of polyphosphates, phosphoric acid, acetic acid, lactic acid and citric acid.
- More preferably the single part concentrated developer composition above comprises an auxiliary developing agent selected from the class of substituted pyrazolidone and para-aminophenol compounds.
- In particular the present invention relates to a single part concentrated developer composition for silver halide photographic materials, to be diluted with water and form a ready-for-use developer solution, comprising:
- (a) hydroquinone or a substituted hydroquinone in an amount from about 40 to 120 grams per liter;
- (b) an auxiliary developing agent in an amount from about 0.5 to 20 grams per liter;
- (c) an alkali metal sulfite in an amount from about 80 to 200 grams per liter;
- (d) an alkanolamine in an amout from about 40 to 120 grams per liter;
- (e) a mixture of benzotriazole and 1-phenyl-5-mercaptotetrazole antifoggant agents in an amount from about 0.8 to 6 grams per liter;
- (f) a sequestering agent selected in the group of DTPA, DPTA and HEDP in an amount from about 20 to 150 grams per liter;
- (g) a compound selected in the group of polyphosphates, phosphoric acid, acetic acid, lactic acid and citric acid, in an amount from about 50 to 150 grams per liter;
- (h) inorganic alkali agents sufficient to provide a pH of at least 11; and
- (i) water sufficient to make up 1 liter.
- The developing agents for silver halide photographic elements suitable for the purposes of the present invention include hydroquinone and substituted hydroquinones (e.g. t-butylhydroquinone, methylhydroquinone, dimethylhydroquinone, chlorohydroquinone, dichlorohydroquinone, bromohydroquinone, 1,4-dihydroxynaphthalene, methoxyhydroquinone, ethoxyhydroquinone, etc.). Hydroquinone, however, is preferred. Said silver halide developing agents are generally used in an amount from about 5 to 50, preferably 10 to 30 grams per liter of the developing solution.
- Such developing agents can be used alone or in combination with auxiliary developing agents which show a superadditive developing effect, such as p-aminophenol and substituted p-aminophenols (e.g. N-methyl-p-aminophenol or metol and 2,4-diaminophenol) and pyrazolidones (e.g. 1-phenyl-3-pyrazolidone or phenidone) and substituted pyrazolidones (e.g. 4-methyl-l-phenyl-3-pyrazolidone and 4,4'-dimethyl-1-phenyl--3-pyrazolidone). Phenidone, however, is preferred. These auxiliary developing agents are generally used in an amount from about 0.1 to 15, preferably 0.2 to 5 grams per liter of the developer.
- The alkali metal sulfites, useful in the developer formulation of this invention as preservatives, include for example sodium and potassium metabisulfite. These are used in an amount from about 15 to 100, preferably 20 to 50 grams per liter of the developer solution.
- The organic antifoggant agents, known in the art to eliminate fog on the developed photographic silver halide films, useful in the developer formulations of this invention include derivatives of benzimidazole, benzotriazole, tetrazole, indazole, thiazole, etc. It has been found, however, that particular mixtures of these antifoggant agents are particularly useful in the developer formulations of this invention to assure low fog levels in any working condition and in case of fast silver halide emulsion films having a greater tendency to fog. Such preferred mixtures include mixtures of 5-nitroindazole and benzimidazole nitrate, 5-nitrobenzotriazole and I-phenyl-5-mercaptotetrazole and benzotriazole and 1-phenyl-5-mercaptotetrazole. The most preferred combination is benzotriazole and 1-phenyl-5-mercaptotriazole, especially when the developer composition ready for use undergoes a storage prolonged in time, for instance more than 15 days at room temperature, before being used. These mixtures are used in a total .amount of from about 0.1 to 3, preferably 0.2 to 1.5 grams per liter of the developer composition. Of course optimum quantities of each compound and proportions can be found by the skilled in the art to respond to specific technical needs. It has been observed, for example, that an excess of l-phenyl-5-tcercaptotetrazole may cause or induce some solarization process especially while developing a color reversal film in a conventional first black-and-white development within a color reversal process. Analogously, an excess of benzotriazole has been found to be related to a decrease of maximum density.
- It has been observed, as well, that 5-nitroindazole and benzimidazole give particularly good results when used together in mixtures which contain from 20 to 80 percent (in weight) of one of them with respect to the total mixture. Additionally, benzotriazole and 5-nitrobenzotriazole have been found to give the best results when used in mixture with 1-phenyl-5-mercaptotetrazole, the latter being present in minor amount with respect to the total mixture, for example in a percent of less than 20 percent, preferably less than 10 percent.
- Inorganic alkali agents are used in the developer formulations of this invention to achieve the preferred pH range which is above 10. Such inorganic alkali agents include KOH, NaOH, potassium and sodium carbonate, etc.
- Other adjuvants well known in the art can be used in the developer formulation of the present invention; these include restrainers, such as soluble halides (e.g. KBr and NaBr), solvents, buffers (e.g. borates and carbonates), development accelerators, and the like.
- In order to be stable to aerial oxidation even during working at high temperatures in continuous transport processing machines, the developer compositions according to the present invention are characterized by the combination of an alkanolamine with the selected sequestering agents above. Alkanolamines suitable for the purpose of the present invention include the hydroxyalkylamines having the general formula:
- Preferred alkanolamines include 2-benzylaminoethanol, ethanolamine, diethanolamine, triethanolamine, choline chloride, 3-amino-1-propanol, 1-amino-2-propanol, 2-amino-2-methyl-1,3-propanediol, tris-(hydroxymethyl)-aminopropane, 2-methylamino-ethanol, 2-dimethyl- amino-ethanol, 2-ethylamino-ethanol, bis-(2-hydroxypropyl)-amine, 3-dimethylamino-1-propanol and 2-isopropylaminomethanol. Most preferred alkanolamines include the ethanolamines such as diethanolamine, triethanolamine, methylaminoethanol, ethylaminoethanol, isopropylamino- ethanol and benzylaminoethanol. The alkanolamines are used in an amount from about 10 to 30, preferably 15 to 20 grams per liter of the developer composition.
- The sequestering agents which combined with alkanolamines render the developer composition more stable to aerial oxidation are selected from the group of diethylenetetraminepentacetic acid (DTPA), 1,3-diamino-2-propanoltetracetic acid (DPTA) and l-hydroxyethyliden-1,1'-diphosphonic acid (HEDP). A still more stable combination in addition includes a compound selected from the group of polyphosphates, phosphoric acid, acetic acid, lactic acid and citric acid. The sequestering agents of the former group are used in an amount from about 5 to 50, preferably 10 to 30 grams per liter of the developer solution and the compounds of the latter are used in an amount from about 5 to 100, preferably 15 to 50 grams per liter of the developer solution. Sequestering agents such as ethylenediaminotetracetic acid (EDTA), nitrilotriacetic acid (NTA) and nitrilotrimethylenephosphonic acid (NTPA), having chemical structures similar to those of some compounds of the former group, and compounds such as aminoacetic acid, oxalic acid, glycolic acid, malic acid, aspartic acid, glutammic acid and tartaric acid, having chemical structures similar to those of some compounds of the latter group, used in combination with alkanolamines, did not prove to be as effective as the selected ones in order to prevent developer degradation.
-
- Exposed black-and-white silver halide photographic films (e.g. Rapid Access films, X-ray films, Printing Papers, Reversal films) can be satisfactorily processed in machines containing the above reported developer solutions to yield high consistency in terms of sensitometric properties (speed, contrast, fog and maximum density) even if the developer solution is left in the machine processor for several days.
- The developer formulation of the present invention may also be prepared from concentrated parts to be diluted with water and form the working solution just prior to its use. Such concentrated parts must be stable in the various storage conditions; problems may arise in making a single concentrated part of the developer solution as such for stability and it is normal practice in the art to divide and package it in two concentrated parts. These parts are combined and diluted with water to the desired strength and placed in the developing tank of the machine.
- We have found that the developer formulations of the present invention may be advantageously prepared in a single concentrated part comprising a mixture of benzotriazole and 1-phenyl-5-mercaptotetrazole as antifoggant agent. When such single concentrated part is diluted with water to a working strength, a developer solution is obtained which assures low fog levels in any working conditions. The greater tendency of fast emulsion films to fog when processed at high temperature in continuous transport processing machines has been more effectively countered by said mixture of organic antifoggant agents. Of course, when the developer solution is made by two concentrated parts (a first part comprising the developing agents, the alkali metal sulfite, the alkanolamine and the sequestering agents and a second part comprising the organic antifoggant agents) the choice of such organic antifoggant agents appears not so critical and any mixture of antifoggant agents above described may be used.
-
- The following examples, which further illustrate the present invention, report some experimental data in order to show the stability to aerial oxidation of the developer formulation of the present invention. In particular, the wavelength (in nm) at which the absorption of 100 ml of developer solution stored 3 days in a 1,000 ml conical flask in contact with air became 100% and the variation of pH between fresh and stored developer solution were measured. It is in fact well known that aerial oxidation of alkaline developers containing hydroquinone results in the liberation of alkali (and hence the pH will tend to rise) and in the darkening of the solution. In order to render more critical the aerial oxidation, in some experiments the developer solutions were added with small amounts of iron salts in addition to metal traces that may be present in water or in the chemicals used to compound the solutions. Examples of the present invention indicated with have been prepared and/or evaluated together with examples of comparative nature indicated with " 1.
-
-
- The developer solutions containing diethanolamine alone or in combination with EDTA and NTA and the solutions containing DTPA, DPTA, EDTA, NTA and HEDP alone, at the end of the experiment, resulted to be strongly colored and all showed a pH increase higher than 0.5. The solutions containing diethanolamine in combination with DTPA, DPTA and HEDP, on the contrary, resulted to be substantially colorless and showed a pH increase lower than 0.5.
-
- The developer solution containing DTPA alone, at the end of the experiment, resulted to be strongly colored and showed a pH increase higher than 0.5. The solutions containing DTPA in combination with diethanolamine or triethanolamine, on the contrary, resulted to be substantially colorless and showed a pH increase lower than 0.5.
-
-
-
-
- 1,000 ml of developers XVII and XVIII were each stored in a 1,500 ml porcelain capsule at room temperature for 3 days.
-
-
- A liquid concentrated developer (Concentrated Developer XIX), consisting of two parts, was prepared as follows:
-
-
- A third liquid concentrated developer (Concentrated Developer XXI), consisting of two parts, was prepared as follows:
-
-
-
- pH at 20°C = 10.97.
-
- Ten ready-for-use developers were prepared from the above concentrated developers according to the following Table 10:
- (follows Table 10)
- Sheets of unexposed 3M LOC4 Contact Film were developed in the above described ready-for-use developers for 60" at 35°C, treated in a stop bath comprising 4% acetic acid for 15" at 35°C, fixed in 3M Fix Roll M for 30" at 35°C and finally washed for 5' at 35°C.
-
- Six black-and-white developers were prepared according to the following formula. The sequestering power versus Fe++ (tested with (NH4)2Fe(SO4)2) were measured: the values thereof are reported hereinbelow in Table 12.
- (follows Table 12)
-
- Seven developer compositions for rapid access processing machines were prepared according to the following Table 13:
- (follows Table 13)
- 100 ml of each developer were stored at room conditions in a 1,000 ml conical flask in contact with air. ΔpH after 24 hour storage; absorption λmax after 72 hour storage; time to reach W100 = 600; and fog of an unexposed 3M LOC4 Film, developed for 60" at 35°C in the above fresh developers (fixed as described in Example 8), were measured. The values are reported in the following Table 14.
- The above times to have W100=600 are well sufficient to maintain the stability of the developer solution left in the processing machine without working during interruptions (e.g. during week-ends). Of course, in the normal working conditions a much longer stability of the developer solution (e.g. one or two months) is secured by the replenishment operation; said stability results in any case higher in the presence of the combination of the alkanolamines and the selected sequestering agents according to the present invention.
Claims (11)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT65213/83A IT1175017B (en) | 1983-09-20 | 1983-09-20 | DEVELOPMENT COMPOSITIONS FOR PHOTOGRAPHIC MATERIALS WITH SILVER HALIDES |
IT6521383 | 1983-09-20 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0136582A2 true EP0136582A2 (en) | 1985-04-10 |
EP0136582A3 EP0136582A3 (en) | 1987-09-23 |
EP0136582B1 EP0136582B1 (en) | 1989-07-19 |
Family
ID=11297753
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP84110559A Expired EP0136582B1 (en) | 1983-09-20 | 1984-09-05 | Developer compositions for silver halide photographic materials |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0136582B1 (en) |
AR (1) | AR244894A1 (en) |
CA (1) | CA1264976A (en) |
DE (1) | DE3479063D1 (en) |
IT (1) | IT1175017B (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0223883A1 (en) * | 1985-11-26 | 1987-06-03 | Agfa-Gevaert N.V. | Method for developing an exposed photographic silver halide emulsion material |
EP0286874A1 (en) * | 1987-04-13 | 1988-10-19 | Minnesota Mining And Manufacturing Company | Developer compositions for silver halide photographic materials |
US4987060A (en) * | 1989-04-03 | 1991-01-22 | Minnesota Mining And Manufacturing Company | Concentrated photographic developer composition and method of making it |
EP0446457A3 (en) * | 1990-03-12 | 1992-02-26 | Minnesota Mining And Manufacturing Company | Alkaline black-and-white photographic developer |
EP0518627A1 (en) * | 1991-06-10 | 1992-12-16 | International Paper Company | Reducing silver sludging during photographic processing |
EP0580041A2 (en) | 1992-07-10 | 1994-01-26 | Fuji Photo Film Co., Ltd. | Method of processing silver halide photographic material and composition for processing |
EP0589460A1 (en) | 1992-09-24 | 1994-03-30 | Fuji Photo Film Co., Ltd. | Method for processing a black & white silver halide light-sensitive material |
EP0654705A2 (en) | 1993-11-24 | 1995-05-24 | Fuji Photo Film Co., Ltd. | Photographic processing composition and method of photographic processing using the same |
US5846687A (en) * | 1995-03-21 | 1998-12-08 | Agfa-Gevaert N.V. | Kit for preparing a processing liquid to be used for making a lithographic printing plate according to the silver salt diffusion transfer process |
EP1227366A1 (en) * | 2001-01-24 | 2002-07-31 | Eastman Kodak Company | Black-and-white developing compositions and methods of use |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1216854A (en) * | 1967-05-05 | 1970-12-23 | Kodak Ltd | Photographic developer composition |
US3576633A (en) * | 1967-06-27 | 1971-04-27 | Eastman Kodak Co | Photographic process and compositions |
GB1376600A (en) * | 1971-02-15 | 1974-12-04 | Agfa Gevaert | Photographic developer compositions |
US4172728A (en) * | 1977-12-16 | 1979-10-30 | E. I. Du Pont De Nemours And Company | High contrast continuous tone developer and process of use |
GB2027920B (en) * | 1978-08-11 | 1983-02-02 | Kodak Ltd | Photographic silver halide developer composition |
-
1983
- 1983-09-20 IT IT65213/83A patent/IT1175017B/en active
-
1984
- 1984-09-05 DE DE8484110559T patent/DE3479063D1/en not_active Expired
- 1984-09-05 EP EP84110559A patent/EP0136582B1/en not_active Expired
- 1984-09-19 CA CA000463575A patent/CA1264976A/en not_active Expired
- 1984-09-19 AR AR84298008A patent/AR244894A1/en active
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0223883A1 (en) * | 1985-11-26 | 1987-06-03 | Agfa-Gevaert N.V. | Method for developing an exposed photographic silver halide emulsion material |
EP0286874A1 (en) * | 1987-04-13 | 1988-10-19 | Minnesota Mining And Manufacturing Company | Developer compositions for silver halide photographic materials |
US4873180A (en) * | 1987-04-13 | 1989-10-10 | Minnesota Mining And Manufacturing Company | Developer compositions for silver halide photographic materials comprising cyclic amino methane diphosphonic acid compounds |
US4987060A (en) * | 1989-04-03 | 1991-01-22 | Minnesota Mining And Manufacturing Company | Concentrated photographic developer composition and method of making it |
EP0391154A3 (en) * | 1989-04-03 | 1991-10-09 | Minnesota Mining And Manufacturing Company | Concentrated photographic developer composition and method of making it |
EP0446457A3 (en) * | 1990-03-12 | 1992-02-26 | Minnesota Mining And Manufacturing Company | Alkaline black-and-white photographic developer |
EP0518627A1 (en) * | 1991-06-10 | 1992-12-16 | International Paper Company | Reducing silver sludging during photographic processing |
EP0580041A2 (en) | 1992-07-10 | 1994-01-26 | Fuji Photo Film Co., Ltd. | Method of processing silver halide photographic material and composition for processing |
EP0589460A1 (en) | 1992-09-24 | 1994-03-30 | Fuji Photo Film Co., Ltd. | Method for processing a black & white silver halide light-sensitive material |
EP0654705A2 (en) | 1993-11-24 | 1995-05-24 | Fuji Photo Film Co., Ltd. | Photographic processing composition and method of photographic processing using the same |
US5846687A (en) * | 1995-03-21 | 1998-12-08 | Agfa-Gevaert N.V. | Kit for preparing a processing liquid to be used for making a lithographic printing plate according to the silver salt diffusion transfer process |
EP1227366A1 (en) * | 2001-01-24 | 2002-07-31 | Eastman Kodak Company | Black-and-white developing compositions and methods of use |
US6602655B2 (en) | 2001-01-24 | 2003-08-05 | Eastman Kodak Company | Black-and-white developing compositions and methods of use |
Also Published As
Publication number | Publication date |
---|---|
EP0136582B1 (en) | 1989-07-19 |
IT1175017B (en) | 1987-07-01 |
DE3479063D1 (en) | 1989-08-24 |
EP0136582A3 (en) | 1987-09-23 |
IT8365213A0 (en) | 1983-09-20 |
AR244894A1 (en) | 1993-11-30 |
CA1264976A (en) | 1990-01-30 |
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