US3865591A - General purpose developer - Google Patents
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- US3865591A US3865591A US358936A US35893673A US3865591A US 3865591 A US3865591 A US 3865591A US 358936 A US358936 A US 358936A US 35893673 A US35893673 A US 35893673A US 3865591 A US3865591 A US 3865591A
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- 239000000203 mixture Substances 0.000 claims abstract description 90
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims abstract description 40
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 31
- -1 silver halide Chemical class 0.000 claims abstract description 29
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical compound O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229910052709 silver Inorganic materials 0.000 claims abstract description 21
- 239000004332 silver Substances 0.000 claims abstract description 21
- 150000002083 enediols Chemical class 0.000 claims abstract description 20
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 9
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000003755 preservative agent Substances 0.000 claims abstract description 8
- 239000000837 restrainer Substances 0.000 claims abstract description 8
- 230000002335 preservative effect Effects 0.000 claims abstract description 7
- 239000006172 buffering agent Substances 0.000 claims abstract description 6
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 36
- 239000004615 ingredient Substances 0.000 claims description 27
- 239000002253 acid Substances 0.000 claims description 25
- 229960005070 ascorbic acid Drugs 0.000 claims description 16
- 235000010323 ascorbic acid Nutrition 0.000 claims description 15
- 239000011668 ascorbic acid Substances 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 15
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 claims description 14
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 13
- 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 claims description 13
- 239000011734 sodium Substances 0.000 claims description 13
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 11
- CRTGSPPMTACQBL-UHFFFAOYSA-N 2,3-dihydroxycyclopent-2-en-1-one Chemical compound OC1=C(O)C(=O)CC1 CRTGSPPMTACQBL-UHFFFAOYSA-N 0.000 claims description 10
- XIWMTQIUUWJNRP-UHFFFAOYSA-N amidol Chemical compound NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 claims description 10
- 150000003141 primary amines Chemical class 0.000 claims description 10
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 9
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-araboascorbic acid Natural products OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 claims description 9
- 229910021538 borax Inorganic materials 0.000 claims description 9
- 235000010350 erythorbic acid Nutrition 0.000 claims description 9
- 239000004328 sodium tetraborate Substances 0.000 claims description 9
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 9
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 8
- 239000004902 Softening Agent Substances 0.000 claims description 8
- JSYBAZQQYCNZJE-UHFFFAOYSA-N benzene-1,2,4-triamine Chemical compound NC1=CC=C(N)C(N)=C1 JSYBAZQQYCNZJE-UHFFFAOYSA-N 0.000 claims description 8
- 239000012964 benzotriazole Substances 0.000 claims description 8
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims description 8
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical group N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- XBDZRROTFKRVES-UHFFFAOYSA-N 2,3-dihydroxy-4,4,5,5-tetramethylcyclopent-2-en-1-one Chemical compound CC1(C)C(O)=C(O)C(=O)C1(C)C XBDZRROTFKRVES-UHFFFAOYSA-N 0.000 claims description 7
- BKMMTJMQCTUHRP-UHFFFAOYSA-N 2-aminopropan-1-ol Chemical compound CC(N)CO BKMMTJMQCTUHRP-UHFFFAOYSA-N 0.000 claims description 7
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 claims description 7
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 6
- SRCQQKFHSKCPGH-UHFFFAOYSA-N 2-amino-4-methyl-6-(methylamino)phenol Chemical compound CNC1=CC(C)=CC(N)=C1O SRCQQKFHSKCPGH-UHFFFAOYSA-N 0.000 claims description 6
- BLFRQYKZFKYQLO-UHFFFAOYSA-N 4-aminobutan-1-ol Chemical compound NCCCCO BLFRQYKZFKYQLO-UHFFFAOYSA-N 0.000 claims description 6
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 claims description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 6
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 6
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 claims description 6
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical group [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 claims description 6
- DPKOCFTZJRJTQL-UHFFFAOYSA-N 2,4-diamino-5-methylphenol Chemical compound CC1=CC(O)=C(N)C=C1N DPKOCFTZJRJTQL-UHFFFAOYSA-N 0.000 claims description 5
- WSVFDPKNANXQKM-UHFFFAOYSA-N 2,4-diamino-6-methylphenol Chemical compound CC1=CC(N)=CC(N)=C1O WSVFDPKNANXQKM-UHFFFAOYSA-N 0.000 claims description 5
- RWAOPZVGICHCOI-UHFFFAOYSA-N 2,4-diaminobenzene-1,3-diol Chemical compound NC1=CC=C(O)C(N)=C1O RWAOPZVGICHCOI-UHFFFAOYSA-N 0.000 claims description 5
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 claims description 5
- MAAWICPSBCHRQR-UHFFFAOYSA-N 4-amino-2-methyl-6-(methylamino)phenol Chemical compound CNC1=CC(N)=CC(C)=C1O MAAWICPSBCHRQR-UHFFFAOYSA-N 0.000 claims description 5
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 5
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 5
- NVIFVTYDZMXWGX-UHFFFAOYSA-N sodium metaborate Chemical group [Na+].[O-]B=O NVIFVTYDZMXWGX-UHFFFAOYSA-N 0.000 claims description 5
- DINKXUCRJBUQAZ-UHFFFAOYSA-N tert-butyl 5-bromopyridine-3-carboxylate Chemical compound CC(C)(C)OC(=O)C1=CN=CC(Br)=C1 DINKXUCRJBUQAZ-UHFFFAOYSA-N 0.000 claims description 5
- BNZCDZDLTIHJAC-UHFFFAOYSA-N 2-azaniumylethylazanium;sulfate Chemical group NCC[NH3+].OS([O-])(=O)=O BNZCDZDLTIHJAC-UHFFFAOYSA-N 0.000 claims description 4
- 229940026239 isoascorbic acid Drugs 0.000 claims description 4
- 235000019982 sodium hexametaphosphate Nutrition 0.000 claims description 4
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 claims description 4
- KQEIJFWAXDQUPR-UHFFFAOYSA-N 2,4-diaminophenol;hydron;dichloride Chemical group Cl.Cl.NC1=CC=C(O)C(N)=C1 KQEIJFWAXDQUPR-UHFFFAOYSA-N 0.000 claims description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 3
- 239000004327 boric acid Substances 0.000 claims description 3
- 239000000839 emulsion Substances 0.000 claims description 3
- 125000000687 hydroquinonyl group Chemical group C1(O)=C(C=C(O)C=C1)* 0.000 claims description 3
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Inorganic materials [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 claims description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 3
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims description 2
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 claims description 2
- 235000019252 potassium sulphite Nutrition 0.000 claims description 2
- 235000010265 sodium sulphite Nutrition 0.000 claims description 2
- ODCGBUMJJJMWBJ-UHFFFAOYSA-N 5-(dimethylamino)-2-(methylamino)phenol Chemical compound CNC1=CC=C(N(C)C)C=C1O ODCGBUMJJJMWBJ-UHFFFAOYSA-N 0.000 claims 3
- DUPRNVZNPMWDDU-UHFFFAOYSA-N 5-methylbenzene-1,2,4-triamine Chemical compound CC1=CC(N)=C(N)C=C1N DUPRNVZNPMWDDU-UHFFFAOYSA-N 0.000 claims 3
- ZNHBMOUCJIUSNM-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanol;ethane-1,2-diamine Chemical compound NCCN.OCCN(CCO)CCO ZNHBMOUCJIUSNM-UHFFFAOYSA-N 0.000 claims 1
- 239000002904 solvent Substances 0.000 abstract description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- 229960004337 hydroquinone Drugs 0.000 description 11
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 8
- 125000003118 aryl group Chemical group 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 150000003254 radicals Chemical class 0.000 description 6
- FJWJYHHBUMICTP-UHFFFAOYSA-N 4,4-dimethylpyrazolidin-3-one Chemical compound CC1(C)CNNC1=O FJWJYHHBUMICTP-UHFFFAOYSA-N 0.000 description 5
- 150000002790 naphthalenes Chemical class 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 229940116357 potassium thiocyanate Drugs 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 229910001514 alkali metal chloride Inorganic materials 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 229940005740 hexametaphosphate Drugs 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 2
- OZHIYEINSCNALY-UHFFFAOYSA-N 1-aminobutan-1-ol Chemical compound CCCC(N)O OZHIYEINSCNALY-UHFFFAOYSA-N 0.000 description 1
- VOSLIUIVGWBSOK-UHFFFAOYSA-N 1-n-phenylbenzene-1,2,4-triamine Chemical compound NC1=CC(N)=CC=C1NC1=CC=CC=C1 VOSLIUIVGWBSOK-UHFFFAOYSA-N 0.000 description 1
- PCAXITAPTVOLGL-UHFFFAOYSA-N 2,3-diaminophenol Chemical class NC1=CC=CC(O)=C1N PCAXITAPTVOLGL-UHFFFAOYSA-N 0.000 description 1
- QSCDISPKCBTNDK-UHFFFAOYSA-N 5-phenylpyrazolidin-3-one Chemical compound N1NC(=O)CC1C1=CC=CC=C1 QSCDISPKCBTNDK-UHFFFAOYSA-N 0.000 description 1
- 101100448208 Human herpesvirus 6B (strain Z29) U69 gene Proteins 0.000 description 1
- 239000002211 L-ascorbic acid Substances 0.000 description 1
- 235000000069 L-ascorbic acid Nutrition 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 150000005205 dihydroxybenzenes Chemical class 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008233 hard water Substances 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000005429 oxyalkyl group Chemical group 0.000 description 1
- 239000006179 pH buffering agent Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 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
- G03C5/30—Developers
Definitions
- 96/66.3, 96/66 R, 96/66 HD agents a -py a dihydroxybenzene. and 511 1111. c1 603C 5/30 an enediol an inorganic Sulfite preservative. 9 buff- [58] Field Of Search 96/66.3, 66 HD, 66 R ering agent, a Silver halide Solvent 9 graininess reducing agent, and a restrainer.
- the developing agent When adjusted to the pH 5 References Cited range 8 to 9.5, the developing agent is effective to in- UNITED STATES PATENTS crease the exposure index of films by a factor of 3.2 2 685 515 H W1 96/66 3 4.2 while at the same time producing images having a 1son 3,276,875 10/1966 Schwalenstocker 1 96/66 R good denslty range and good Shadow detail 3,615,440 10/1971 Bloom 96/66 R 27 Claims, N0 Drawings GENERAL PURPOSE DEVELOPER BACKGROUND OF THE INVENTION 1.
- the present invention relates to silver halide photographic developer compositions and, more particularly, to developer compositions which increase the exposure index of film (EL).
- the Schwallenstocker composition when used to develop commercially available film emulsions, notwithstanding the unusually large quantity of antifoggant, the negative is commercially unacceptable due to gross fog. To reduce the fog to acceptable levels requires the addition of additional anti-foggant until the benzotriazole concentration level reaches about 28 grams per liter. Although at a developer level of 46 grams per liter and an anti-foggant level of 28 grams per liter acceptable images can be produced without appreciable fog, it will be appreciated that such a developer composition is totally impractical. Thus the composition was diluted to a reasonable l-phenyl-3- pyrazolidone concentration level of about one gram per liter, at which level although development and fog were satisfactory, there was no increase noted in the exposure index of films developed therein.
- the present invention in its preferred embodiment provides a developer composition
- a developer composition comprising three de veloping agents a 3-pyrazolidone, a dihydroxybenzene, and an enediol an inorganic sulfite preservative, a buffering agent, a silver halide solvent, a graininess reducing agent, and a restrainer.
- the developing agent When adjusted to the pH range 8 to 9.5, the developing agent is effective to increase the exposure index (E.l.) of films while at the same time producing images having a broad density range and good shadow detail.
- the present invention in its broadest form, provides an alkaline developer composition, pH 8 to 9.5, containing at least three developing agents.
- Table 1 sets forth the ingredients and proportion ranges at which useful results, in terms of increased exposure index without adverse side effects, are obtained.
- the silver halide developing agents employed in accordance with the present invention are selected, one
- R groups each represent various substitu- -bon atoms, or an aryl group such as phenyl.
- Phenidone is the preferred member of the 3-pyrazolidone class of agents for use in the present invention. Phenidone is preferred because it is commercially availablein large quantities while other known, related developing agents having similar structure and characteristics are not widely available.
- the following compounds are representative of 3-pyrazolidone silver halide developing agents which are useful in the developer compositions of this invention:
- Z is a divalent aliphatic grouping which, with the carbon atoms in 4 and 5 positions of the pyrazolidone ring, completes a five membered or sixmembered cycloaliphatic ring and R is an aryl group e.g., phenyl or naphthyl group.
- aryl groups may be substituted with 'hydroxy, alkoxy, oxyalkyl, amino, substituted amino, nitro, sulphonic or carboxylic groups or halogen atoms.
- These compounds include, for example, l-phenyl- 4,5-tetramethylene-3-pyrazolidone, l-phenyl-4,5- trimethylene-3-pyrazolidone and l-mchlorophenyl-4,5-tetramethylene-3-pyrazolidone.
- dihydroxybenzene silver halide developing agents which are useful in the developer compositions of this invention are hydroquinone, resorcinol and pyrocatechol.
- the developer composition includes an inorganic sulfite preservative agent for the developers, such as the sulfites of sodium or potassium; a silver halide solvent, such as sodium or potassium thiocyanate; a graininess reducing salt, such as sodium or lithium chloride; a restrainer, which also serves as a grain reducer, such as sodium or potassium bromide; and a pH buffering agent, such as sodium metaborate, boric acid, acetic acid, sodium carbonate and the like in quantities and combinations sufficient to adjust the developer pH to the desired level within the 8 to 9.5 range.
- an inorganic sulfite preservative agent for the developers such as the sulfites of sodium or potassium
- a silver halide solvent such as sodium or potassium thiocyanate
- a graininess reducing salt such as sodium or lithium chloride
- a restrainer which also serves as a grain reducer, such as sodium or potassium bromide
- a pH buffering agent such as sodium metaborate, boric acid
- a fourth developing agent selected from the aminophenol class may be employed.
- the preferred aminophenol (the term aminophenol will be em ployed hereinafter as generic to amino substituted phenols, including diaminophenols for use in the present invention is 2,4 diaminophenol dihydrochloride, commonly known as amidol.
- amidol is the only member of the class that is manufactured and commercially available in quantity.
- antifoggants such as benzotriazole, borax, which serves both as a fine grain agent and an alkaline buffer; and a water softener where hard water conditions cause flocculation in the developer.
- antifoggants such as benzotriazole, borax, which serves both as a fine grain agent and an alkaline buffer
- borax which serves both as a fine grain agent and an alkaline buffer
- water softener where hard water conditions cause flocculation in the developer.
- sodium hexametaphosphate which may be provided as the commercially available product Calgon, manufactured by the Calgon Corporation. 5
- the primary amines optionally useful in the present invention include ethylamine, monoethanolamine, triethanolamine, ethylenediamine, 2-amino-l-butanol, 2-aminopropanol, 3-aminopropanol and 4.-aminobutanol. Even more desirable are the acid salts of these primary amines formed by reaction with such acids as hydrochloric, nitric, sulfuric, acetic, citric, tartaric, benzoic and ascorbic. Specifically, ethylenediamine sulfate is the preferred amine acid salt component of the developer.
- the useful concentration range of ethylenediamine sulfate is 0 to 10 grams per liter to contribute the indicated 0 to 4 grams per liter of primary amine.
- Table I shows the amine to be an optional ingredient, when included it is effective to reduce silvering on the film, particularly medium and fast Panchromatic films, caused by the presence of silver halide solvents, such as potassium thiocyanate, in the developer. It should be appreciated, however, that when present the amines contribute added fog density to the developed film.
- Example II The developer composition of Example I and a conventional developer, Microdol-X, available commercially from the Eastman Kodak Company, were used to develop the films of Table II after exposure at the listed ASA values (see Table II, column II).
- the images produced by the Microdol-X exhibited good contrast and density and appeared properly developed.
- the images produced by the composition of Example I were much too dark (over exposed) and were generally unacceptable.
- the films listed in Table II were then exposed at exposure settings progressively greater than the listed ASA and the exposed film developed in both Microdol- X and the composition of Example I until an exposure setting was reached when the images produced by the composition of Example I were comparable in quality (i.e., contrast, density, shadow detail, and the like) to the images produced by the Microdol-X at the listed ASA value for each film.
- Column ill of Table ll tabulates the exposure settings at which the comparable results were obtained.
- the images produced by the Microdol-X were extremely thin (under exposed).
- Example I effectively increased the exposure index of the tested films by a factor of not less than about 3.2 and as high as about 4.2 (column lV) without adversely affecting image quality.
- 3-pyrazolidone developer 0.8 m 3 grams dihydroxybenzene developer selected from the group consisting of hydroquinone, resorcinol and pyrocatecl ol,..,.. 8to l4 grams enediol developer selected from the group consisting of ascorbic acid, d-araboascorbic acid, reductic acid, 2-oxytetronic acid, 4-aryl-2-oxytetronic acid, 4-aryl-2-oxytetronimide, isoascorbic acidand enediols having the chemical structure represented by the formula R4 OH R.. c c
- R,, R R and R are selected from the group consisting of hydrogen and the radical CH R R is selected from hydrogen and a monovalent radical selected from the group consisting of amino, cyano, halo, hydroxyl, carboxyl, sulfonyl, alkyl, cycloalkyl, aryl of the benzene or naphthalene series and alkaryl of the benzene or naphthalene series, at least one of said R R R and R being the radical CH2R ..2 to grams inorganic sulfite preservative to 75 grams silver halide solvent selected from sodium and potassium thiocyanate to 2% grams graininess reducer selected from the alkali metal chlorides ..410 30 grams restrainer v. m 2 grams buffering agent 2 to 40 grams.
- composition as claimed in claim 1, wherein said 3-pyrazolidone developer is selected from the developing agents having the following chemical structure:
- R R R R and R are selected from hydrogen, alkyl groups containing from l to 4 carbon atoms and aryl groups selected from the benzene and naphthalene series.
- composition, as claimed in claim 2, wherein said 3-pyrazolidone is l-phenyl-3-pyrazolidone.
- composition, as claimed in claim 1, wherein said enediol is selected from tetramethyl reductic acid and ascorbic acid.
- composition as claimed in claim 5, wherein said inorganic sulfite preservative is selected from sodium and potassium sulfite.
- composition as claimed in claim 5, wherein said graininess reducer is selected from sodium and lithium chloride.
- composition as claimed in claim 5, wherein said restrainer is selected from sodium and potassium bromide.
- composition as claimed in claim 5, wherein said buffering agent is selected from sodium metaborate, boric acid, acetic acid, sodium carbonate and mixtures thereof.
- composition as claimed in claim 5, further including at least one of the following ingredients:
- an aminophenol developer selected from the group consisting of paminophenol, N-methyl-p-amino phenol, 2,4- diaminophenol, 2,4-diaminoresorcinol, 6-methyl- 2,4-diaminophenol, 5-methyl-2,4-diaminophenol, 4-amino-6-methyl-2-methylaminophenol, 6-amino- 4-methyl-2-methylaminophenol, S-dimethylamino- 2-methylaminophenol, 1,2,4-triaminobenzene, 5- methyl-l,2,4-t:iaminobenzene, 4-hydroxy,2',4- diaminodiphenylamine, 4,2',4'- triaminodiphenylamine, l,3-diamino-4,7- dihydroxybenzene, and the acid salts thereof;
- a primary amine selected from the group consisting of ethylamine, monoethanolamine, triethanolamine, ethylenediamine, 2- amino-l-butanol, 2-aminopropanol, 3- aminopropanol, 4-amino-butanol and the acid salts thereof;
- a composition, as claimed in claim 11 wherein said additional ingredient is an aminophenol developer selected from the group consisting of p-aminophenol, N-methyl-paminophenol, 2,4-diaminophenol, 2,4- diaminoresorcinol, 6-methyl-2,4-diaminophenol, 5-methyl-2,4-diaminophenol, 4-amino-6-methyl-2- methylaminophenol, 6-amino-4-methyl-2- methylaminophenol, S-dimethylamino-Z- methylaminophenol, l,2,4-triaminobenzene, 5methyl l,2,4-triaminobenzene, 4-hydroxy,2 ,4- diaminodiphenylamine, 4,2',4'- triaminodiphenylamine, l,3-diamino-4,7- dihydroxybenzene, and the acid salts thereof.
- aminophenol developer selected from the group consisting of p-aminophenol, N-
- a composition, as claimed in claim 11 wherein said additional ingredient is a primary amine selected from the group consisting of ethylamine, monoethanolamine, triethanolamine, ethylenediamine, 2-aminolbutanol, 2-aminopropanol, 3-aminopropanol, 4-aminobutanol and the acid salts thereof.
- composition as claimed in claim 11, wherein said additional ingredient is benzotriazole.
- composition as claimed in claim 11, wherein said additional ingredient is borax.
- composition as claimed in claim 11, wherein said additional ingredient is a water softening agent.
- a silver halide photographic developing composition comprising the following ingredients in the weight.
- a silver halide photographic developing composition comprising the following ingredients in the weight proportion ranges indicated per liter of composition:
- a photographic developing process for increasing the exposure index of an imagewise exposed silver halide emulsion film comprising developing said film in an aqueous silver halide photographic developing composition having a pH in the range 8 9.5.
- said developing composition comprising the following ingredients in the weight proportion ranges indicated per liter of composition:
- B-pyrazolidone developer 0.8 to 3 grams dihydroxybenzene developer selected from the group consisting of hydroquinone, resorcinol and pyrocatechol 8 to l4 grams enediol developer selected from the group consisting of ascorbic acid, d-araboascorbic acid, reductic acid, 2-oxytetronic acid, 4-aryl-2-oxytetronic acid, 4-aryl-2-oxytetronimide, isoascorbic acid and enediols having the chemical structure represented by the formula wherein R R R and R, are selected from the group consisting of hydrogen and the radical -Cl-l R R is selected from hydrogen and a monovalent radical selected from the group consisting of amino, cyano, halo, hydroxyl, carboxyl, sulfonyl, alkyl, cycloalkyl, aryl of the benzene or naphthalene series and alkaryl of the benzene or naphthalene series, at least one
- R R R R and R are selected from hydrogen, alkyl groups containing from 1 to 4 carbon atoms and aryl groups selected from the benzene and naphpyrazolidone is l-phenyl-3-pyrazolidone and said enea diol is selected from the group consisting of tetramethyl reductic acid and ascorbic acid.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Abstract
Description
Claims (27)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US358936A US3865591A (en) | 1973-05-10 | 1973-05-10 | General purpose developer |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US358936A US3865591A (en) | 1973-05-10 | 1973-05-10 | General purpose developer |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3865591A true US3865591A (en) | 1975-02-11 |
Family
ID=23411643
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US358936A Expired - Lifetime US3865591A (en) | 1973-05-10 | 1973-05-10 | General purpose developer |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3865591A (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2344874A1 (en) * | 1976-03-15 | 1977-10-14 | Anneman William | Low contrast developer for high contrast silver halide emulsion - with (micro)fine grains contains pyrazolidone, hydroquinone, metol etc. |
| US4083722A (en) * | 1976-03-15 | 1978-04-11 | William Alexander Anneman | Developer composition and process for developing photographic film |
| WO1993012463A1 (en) * | 1991-12-12 | 1993-06-24 | Kodak Limited | Photographic developer stabilisation |
| US5385811A (en) * | 1993-04-27 | 1995-01-31 | Fuji Photo Film Co., Ltd. | Method for processing silver halide photographic materials |
| US5419997A (en) * | 1993-03-05 | 1995-05-30 | Fuji Photo Film Co., Ltd. | Method for processing silver halide photographic material |
| US5478706A (en) * | 1991-04-03 | 1995-12-26 | Minnesota Mining And Manufacturing Company | Alkaline black-and-white developer for silver halide photographic material |
| EP0731382A1 (en) * | 1995-02-21 | 1996-09-11 | Agfa-Gevaert N.V. | Method for processing an exposed photographic silver halide material |
| EP0731381A1 (en) * | 1995-02-21 | 1996-09-11 | Agfa-Gevaert N.V. | Developing solution and method for developing an exposed silver halide photographic material |
| EP0732619A1 (en) * | 1995-02-21 | 1996-09-18 | Agfa-Gevaert N.V. | Developing method and method for developing an exposed photographic silver halide material |
| EP0716338A3 (en) * | 1994-12-09 | 1996-09-25 | Fuji Photo Film Co Ltd | Fine polymer particles having heterogeneous phase structure, silver halide photographic light- sensitive material containing the fine polymer particles and image-forming method |
| EP0794456A1 (en) * | 1996-03-07 | 1997-09-10 | Agfa-Gevaert N.V. | Method of reproducing an electronically stored medical image on a light-sensitive photographic material |
| FR2750225A1 (en) * | 1996-06-24 | 1997-12-26 | Kodak Pathe | PHOTOGRAPHIC DEVELOPMENT COMPOSITION |
| US5702875A (en) * | 1996-06-28 | 1997-12-30 | Eastman Kodak Company | Weakly alkaline ascorbic acid developing composition, processing kit and method using same |
| EP0877287A1 (en) * | 1997-05-09 | 1998-11-11 | Konica Corporation | Developer for silver halide light sensitive photographic material and processing method by use thereof |
| US6083673A (en) * | 1996-01-23 | 2000-07-04 | Eastman Kodak Company | Organic/inorganic developer composition |
| US6379877B1 (en) | 1995-02-21 | 2002-04-30 | Agfa-Gevaert | Method for developing an exposed photographic silver halide material |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2685515A (en) * | 1953-08-03 | 1954-08-03 | Eastman Kodak Co | Photographic developer composition |
| US3276875A (en) * | 1963-12-02 | 1966-10-04 | Du Pont | Developing composition with pyrrolidone anti-sludging agent |
| US3615440A (en) * | 1968-10-25 | 1971-10-26 | Polaroid Corp | Novel photographic compositions and processes |
| US3615513A (en) * | 1965-11-01 | 1971-10-26 | Eastman Kodak Co | Inhibition of silvering in photographic processing solutions |
| US3730716A (en) * | 1971-05-19 | 1973-05-01 | Polaroid Corp | Silver image stabilization with noble metal compounds and alpha,beta-enediol developer |
-
1973
- 1973-05-10 US US358936A patent/US3865591A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2685515A (en) * | 1953-08-03 | 1954-08-03 | Eastman Kodak Co | Photographic developer composition |
| US3276875A (en) * | 1963-12-02 | 1966-10-04 | Du Pont | Developing composition with pyrrolidone anti-sludging agent |
| US3615513A (en) * | 1965-11-01 | 1971-10-26 | Eastman Kodak Co | Inhibition of silvering in photographic processing solutions |
| US3615440A (en) * | 1968-10-25 | 1971-10-26 | Polaroid Corp | Novel photographic compositions and processes |
| US3730716A (en) * | 1971-05-19 | 1973-05-01 | Polaroid Corp | Silver image stabilization with noble metal compounds and alpha,beta-enediol developer |
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4083722A (en) * | 1976-03-15 | 1978-04-11 | William Alexander Anneman | Developer composition and process for developing photographic film |
| FR2344874A1 (en) * | 1976-03-15 | 1977-10-14 | Anneman William | Low contrast developer for high contrast silver halide emulsion - with (micro)fine grains contains pyrazolidone, hydroquinone, metol etc. |
| US5478706A (en) * | 1991-04-03 | 1995-12-26 | Minnesota Mining And Manufacturing Company | Alkaline black-and-white developer for silver halide photographic material |
| WO1993012463A1 (en) * | 1991-12-12 | 1993-06-24 | Kodak Limited | Photographic developer stabilisation |
| JP3249521B2 (en) | 1991-12-12 | 2002-01-21 | イーストマン コダック カンパニー | Stabilization of photographic developer |
| US5419997A (en) * | 1993-03-05 | 1995-05-30 | Fuji Photo Film Co., Ltd. | Method for processing silver halide photographic material |
| US5385811A (en) * | 1993-04-27 | 1995-01-31 | Fuji Photo Film Co., Ltd. | Method for processing silver halide photographic materials |
| EP0716338A3 (en) * | 1994-12-09 | 1996-09-25 | Fuji Photo Film Co Ltd | Fine polymer particles having heterogeneous phase structure, silver halide photographic light- sensitive material containing the fine polymer particles and image-forming method |
| US6027805A (en) * | 1994-12-09 | 2000-02-22 | Fuji Photo Film Co., Ltd. | Fine polymer particles having heterogeneous phase structure |
| US5804357A (en) * | 1994-12-09 | 1998-09-08 | Fuji Photo Film Co., Ltd. | Fine polymer particles having heterogeneous phase structure, silver photographic light sensitive material containing the fine polymer particles and image-forming method |
| US6087081A (en) * | 1994-12-09 | 2000-07-11 | Fuji Photo Film Co., Ltd. | Fine polymer particles having heterogeneous phase structure, silver halide photographic light-sensitive material containing the fine polymer particles and image-forming method |
| EP0731382A1 (en) * | 1995-02-21 | 1996-09-11 | Agfa-Gevaert N.V. | Method for processing an exposed photographic silver halide material |
| EP0731381A1 (en) * | 1995-02-21 | 1996-09-11 | Agfa-Gevaert N.V. | Developing solution and method for developing an exposed silver halide photographic material |
| EP0732619A1 (en) * | 1995-02-21 | 1996-09-18 | Agfa-Gevaert N.V. | Developing method and method for developing an exposed photographic silver halide material |
| US6379877B1 (en) | 1995-02-21 | 2002-04-30 | Agfa-Gevaert | Method for developing an exposed photographic silver halide material |
| US6083673A (en) * | 1996-01-23 | 2000-07-04 | Eastman Kodak Company | Organic/inorganic developer composition |
| EP0794456A1 (en) * | 1996-03-07 | 1997-09-10 | Agfa-Gevaert N.V. | Method of reproducing an electronically stored medical image on a light-sensitive photographic material |
| US5780212A (en) * | 1996-06-24 | 1998-07-14 | Eastman Kodak Company | Photographic developing composition |
| EP0816916A1 (en) * | 1996-06-24 | 1998-01-07 | Eastman Kodak Company | Photographic developing composition |
| FR2750225A1 (en) * | 1996-06-24 | 1997-12-26 | Kodak Pathe | PHOTOGRAPHIC DEVELOPMENT COMPOSITION |
| US5702875A (en) * | 1996-06-28 | 1997-12-30 | Eastman Kodak Company | Weakly alkaline ascorbic acid developing composition, processing kit and method using same |
| US5756271A (en) * | 1996-06-28 | 1998-05-26 | Eastman Kodak Company | Weakly alkaline ascorbic acid developing composition, processing kit and method using same |
| US5998112A (en) * | 1997-05-09 | 1999-12-07 | Konica Corporation | Developer for silver halide light sensitive photographic material and processing method by use thereof |
| EP0877287A1 (en) * | 1997-05-09 | 1998-11-11 | Konica Corporation | Developer for silver halide light sensitive photographic material and processing method by use thereof |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: KATZ, JEROME; ROCHESTER, NY. Free format text: CONDITIONAL ASSIGNMENT;ASSIGNOR:DELAWARE PHOTOGRAPHIC PRODUCTS, INC.;REEL/FRAME:004157/0821 Effective date: 19830321 Owner name: KATZ, JEROME, NEW YORK Free format text: CONDITIONAL ASSIGNMENT;ASSIGNOR:DELAWARE PHOTOGRAPHIC PRODUCTS, INC.;REEL/FRAME:004157/0821 Effective date: 19830321 |
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| AS | Assignment |
Owner name: DELAWARE CAMERA MART, INC.; BUFFALO, NY. Free format text: ASSIGNMENT OF 1/2 OF ASSIGNORS INTEREST;ASSIGNOR:DELAWARE PHOTOGRAPHIC PRODUCTS. INC.;REEL/FRAME:004157/0825 Effective date: 19821120 Owner name: DELAWARE CAMERA MART, INC., NEW YORK Free format text: ASSIGNMENT OF 1/2 OF ASSIGNORS INTEREST;ASSIGNOR:DELAWARE PHOTOGRAPHIC PRODUCTS. INC.;REEL/FRAME:004157/0825 Effective date: 19821120 |