US3549364A - Photographic processes and compositions - Google Patents
Photographic processes and compositions Download PDFInfo
- Publication number
- US3549364A US3549364A US690728A US3549364DA US3549364A US 3549364 A US3549364 A US 3549364A US 690728 A US690728 A US 690728A US 3549364D A US3549364D A US 3549364DA US 3549364 A US3549364 A US 3549364A
- Authority
- US
- United States
- Prior art keywords
- silver halide
- silver
- image
- energy
- developing agent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title description 38
- 238000000034 method Methods 0.000 title description 23
- 229910052709 silver Inorganic materials 0.000 description 65
- 239000004332 silver Substances 0.000 description 65
- 239000003795 chemical substances by application Substances 0.000 description 51
- -1 silver halide Chemical class 0.000 description 45
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 28
- 238000012545 processing Methods 0.000 description 27
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 14
- 238000012546 transfer Methods 0.000 description 13
- 239000000839 emulsion Substances 0.000 description 11
- 239000011734 sodium Substances 0.000 description 11
- 229910052708 sodium Inorganic materials 0.000 description 11
- 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 10
- 229940081735 acetylcellulose Drugs 0.000 description 8
- 235000010323 ascorbic acid Nutrition 0.000 description 8
- 229920002301 cellulose acetate Polymers 0.000 description 8
- 238000011161 development Methods 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 6
- 239000012530 fluid Substances 0.000 description 6
- 229940046892 lead acetate Drugs 0.000 description 6
- 230000002195 synergetic effect Effects 0.000 description 6
- 229960005070 ascorbic acid Drugs 0.000 description 5
- 239000011668 ascorbic acid Substances 0.000 description 5
- LHQLJMJLROMYRN-UHFFFAOYSA-L cadmium acetate Chemical compound [Cd+2].CC([O-])=O.CC([O-])=O LHQLJMJLROMYRN-UHFFFAOYSA-L 0.000 description 5
- 238000005213 imbibition Methods 0.000 description 5
- PXTJLOZYMBNREW-UHFFFAOYSA-N 4,6-diamino-6-methylcyclohexa-1,3-dien-1-ol Chemical compound CC1(N)CC(N)=CC=C1O PXTJLOZYMBNREW-UHFFFAOYSA-N 0.000 description 4
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-isoascorbic acid Chemical compound OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 235000010350 erythorbic acid Nutrition 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 229940026239 isoascorbic acid Drugs 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 4
- 229910052979 sodium sulfide Inorganic materials 0.000 description 4
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 4
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 3
- 150000000996 L-ascorbic acids Chemical class 0.000 description 3
- 230000000536 complexating effect Effects 0.000 description 3
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 150000002443 hydroxylamines Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000001376 precipitating effect Effects 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
- PSJZYGKOSQRHPB-UHFFFAOYSA-N 4-amino-2,6-dimethoxyphenol Chemical compound COC1=CC(N)=CC(OC)=C1O PSJZYGKOSQRHPB-UHFFFAOYSA-N 0.000 description 2
- OMVFXCQLSCPJNR-UHFFFAOYSA-N 4-amino-2,6-dimethylphenol Chemical compound CC1=CC(N)=CC(C)=C1O OMVFXCQLSCPJNR-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
- 239000012736 aqueous medium Substances 0.000 description 2
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 2
- 229910001864 baryta Inorganic materials 0.000 description 2
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 2
- 235000018417 cysteine Nutrition 0.000 description 2
- FVCOIAYSJZGECG-UHFFFAOYSA-N diethylhydroxylamine Chemical compound CCN(O)CC FVCOIAYSJZGECG-UHFFFAOYSA-N 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NSSIZMPQSZKECB-UHFFFAOYSA-N (diethoxyamino)oxyethane Chemical compound CCON(OCC)OCC NSSIZMPQSZKECB-UHFFFAOYSA-N 0.000 description 1
- ABLAOHGMWKVEGE-UHFFFAOYSA-N (dimethoxyamino)oxyethane Chemical compound CCON(OC)OC ABLAOHGMWKVEGE-UHFFFAOYSA-N 0.000 description 1
- ZAMLGGRVTAXBHI-UHFFFAOYSA-N 3-(4-bromophenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid Chemical compound CC(C)(C)OC(=O)NC(CC(O)=O)C1=CC=C(Br)C=C1 ZAMLGGRVTAXBHI-UHFFFAOYSA-N 0.000 description 1
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 1
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- FGRVOLIFQGXPCT-UHFFFAOYSA-L dipotassium;dioxido-oxo-sulfanylidene-$l^{6}-sulfane Chemical compound [K+].[K+].[O-]S([O-])(=O)=S FGRVOLIFQGXPCT-UHFFFAOYSA-L 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 229910052981 lead sulfide Inorganic materials 0.000 description 1
- 229940056932 lead sulfide Drugs 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000005406 washing Methods 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
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/02—Photosensitive materials characterised by the image-forming section
- G03C8/04—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of inorganic or organo-metallic compounds derived from photosensitive noble metals
- G03C8/06—Silver salt diffusion transfer
Definitions
- Photographic processes for forming a silver image by diffusion transfer are well known.
- Processes for forming a usable negative image along with the positive silver transfer image are also known.
- a lightsensitive silver halide emulsion which has been exposed to contain a developable image is typically contacted with an aqueous alkaline processing composition including a silver halide solvent and a silver halide developing agent; exposed and developable silver halide is reduced to image silver to form a negative image and at substantially the same time an imagewise distribution of a soluble silver complexe is formed in terms of unexposed areas of the emulsion.
- This imagewise distribution is transferred at least in part, by imbibition, to a superposed image-receiving layer where it is reduced to image silver to form a pOSitive silver transfer image.
- the present invention is directed to developing compositions which obviate or greatly reduce the need for aftertreatment.
- the present invention is directed to processing compositions for use in silver diffusion transfer processes for forming a usable negative image along with a positive silver transfer image, the compositions including the novel combination of a high energy aminophenol silver halide developing agent containing in one or both of the positions ortho to the phenolic hydroxyl group an amino, alkyl or alkoxy group; and a low energy ascorbic acid or hydroxylamine silver halide developing agent, the low energy developing agent being present in substantially greater concentration than the high energy developing agent, the amount of each of the developing agents alone being insufficient to develop appreciable negative density, but the respective amounts together providing a synergistic effect whereby the combination of developing agents in the processing compositions is capable of providing, upon development, a negative image having a desired usable density.
- the processing composition further includes at least one silver halide solvent and at least one alkaline material in sufiicient quantity to provide a pH of at least 10.5.
- the processing composition containing the aforementioned novel combination of silver halide developing agents further includes as the silver halide solvent or complexing ingredients the combination of cysteine and a nitrogenous base, as described and claimed in applicants US. Pat. No. 3,343,958.
- the processing composition is further characterized by having a pH of from 10.5 to about 12.5.
- the present invention is directed to novel processing compositions for use in diffusion transfer systems for preparing a usable negative silver image along with a positive silver transfer image and to photographic processes employing the same.
- a primary object of this invention is to provide novel products and processes of the foregoing description.
- Another object is to provide novel silver halide developing compositions which obviate or greatly reduce the need for after-treatment to obtain stable silver images.
- the invention accordingly comprises the several steps and the relation and order of one or more of such steps with respect to each of the others, and the product possessing the features, properties and the relation of elements which are exemplified in the following detailed disclosure, and the scope of the application of which will be indicated in the claims.
- high-energy silver halide developing agents are known.
- One class of these known high-energy developers are the aminophenols, e.g., 4-amino-phenols having a lower alkyl, lower alkoxy, and/ or an amino group in a position or the positions ortho to the phenolic hydroxyl group.
- Particularly useful examples of such high energy silver halide developing agents include 2,4-diamino-ortho-cresol, 4-amino-2,6-dimethyl-phenol and 2,6-dimethoxyl-4-aminophenol.
- Such a high-energy silver halide developing agent may be employed in extremely low concentrations if it is employed in combination with a high concentration of a low-energy silver halide developing agent.
- the synergistic effects so obtained greatly expands the usefulness of such high-energy silver halide developing agents.
- Particularly useful low-energy silver halide developing agents are those which have substantially colorless oxidation products and/or are volatilized from the image, particularly the ascorbic acids, such as ascorbic acid, isoascorbic acid, etc., and hydroxylamines,
- Suitable hydroxylamine silver halide developing agents include those disclosed in U.S. Patents Nos. 2,857,276, is sued to Edwin H. Land et al., and 3,287,125 issued to Milton Green, Adnan A. Sayigh and Henri Ulrich.
- compositions containing the novel synergistic combination of developing agents of this invention have been found, according to the present invention, to be particularly useful in photographic systems wherein one desires to obtain a fully developed and fixed negative silver image of good density, contrast and stability along with a positive silver transfer image.
- Processing compositions in which the combination of developing agents of this invention are intended to be employed in such processes in general further include a silver halide solvent or fixing agent, e.g., sodium or potassium thiosulfate, etc. and an alkaline material such as sodium hydroxide, diethylamine, sodium carbonate, etc. in an amount suflicient to provide a pH of at least 10.5, preferably from 10.5 to about 12.5 With a pH below about 10.5 the development time is appreciably slower.
- a silver halide solvent or fixing agent e.g., sodium or potassium thiosulfate, etc.
- an alkaline material such as sodium hydroxide, diethylamine, sodium carbonate, etc.
- any of the known complexing ingredients may be contained in the processing compositions contemplated by this invention, of particular use is the combination of complexing ingredients disclosed in my U.S. Patent No. 3,343,958.
- a nitrogenous base e.e., diethylamine
- the processing compositions may also contain additional reagents performing specific desired functions, e.g., viscosity-increasing, film-forming materials such as sodium carboxymethyl cellulose, hydroxyethyl cellulose, etc.; antifoggants, preservatives, toning agents, etc.
- the respective ingredients of the processing composition may be present initially in the aqueous medium therefor, or any or all of them may be present initially in the photographic product, e.g., the photosentitive element or the image-receiving element, in which case the desired composition may be formed by applying thereto the aqueous medium, e.g., during the development step.
- EXAMPLE 1 A photosensitive element having a silver iodobromide emulsion on a film base was exposed and then developed by spreading between the thus exposed emulsion and a superposed surface hydrolyzed cellulose acetate sheet a processing composition comprising the following proportions of ingredients:
- Aqueous solution of sodium sulfide (156mg. Na S/cc.)-
- Aqueous solution of lead acetate and cadmium acetate (100 cc. H O, 2.9 g. lead acetate; 2.1 g. cadmium acetate)0.34 cc.
- the spreader sheet was removed to reveal a fully developed and fixed negative on the photosensitive element and a good quality positive silver transfer image in the solidified layer of processing fluid adhered to the hydrolyzed surface of the cellulose acetate sheet.
- EXAMPLE 2 A photosensive element having a silver iodobromide emulsion on film base was exposed and processed by spreading a layer of processing fluid, approximately 0.0020 thick, between the exposed negative and a surface hydrolyzed sheet of cellulose acetate.
- the processing fluid comprised:
- Aqueous solution of sodium sulfide of sodium sulfide (156 mg. Na S/cc.)0.0l1 cc.
- the cellulose ace tate sheet was separated from the exposed negative to provide a negative silver image, and a positive silver transfer image in a solidified layer of processing fluid adhered to the hydrolyzed surface of the cellulose acetate sheet.
- Aqueous solution of lead acetate and cadmium acetate (100 cc. H O, 2.9 g. lead acetate; 2.1 g. cadmium acetate)0.36 cc.
- EXAMPLE 4 The procedures described in the preceding examples were repeated using baryta paper instead of the cellulose acetate sheet. The solidified layer of processing fluid adhered to the baryta paper when it was separated from the developed negative.
- the silver precipitating nuclei for initiating and facilitating reduction of silver halide to image silver were present initially in the processing fluid.
- Such procedures are described, forexample, in U.S. Patent No. 2,662,822 issued to Edwin H. Land.
- the silver precipitating nuclei may alternatively be present in the silverreceptive stratum, e.g., to provide one of the vigorous silver precipitating environments described, for example, in U.S. Pats. Nos. 2,698,237 and 2,698,245 issued to Edwin H. Land.
- EXAMPLE 5 A photosensitive element having a silver iodobromide emulsion on a film base was exposed and then developed by spreading between the thus-exposed emulsion and a superposed surface hydrolyzed cellulose acetate sheet a processing composition comprising the following proportions of ingredients:
- Example 5 was repeated eliminating the ascorbic acid from the developing composition. An extremely faint (D 0.15 above base density) image was obtained.
- Example 5 was repeated eliminating the 2,4diaminoorthocresol from the developing composition. The resulting image was even fainter or had an even lower density (D 0.05 above base density) than the negative prepared in Example 6.
- the following example represents developing time series analyses illustrating the effect of pH upon development time.
- EXAMPLE 8 A light-sensitive silver iodobromide emulsion was exposed and then developed with a first processing composition having a pH above 11.0 and comprising the following proportions of ingredients:
- a second set of development times were run by exposing and developing a similar light-sensitive emulsion with a second processing composition in which the amounts of sodium hydroxide and diethylamine were adjusted so that the processing composition had a pH of 8.5 to 9.0.
- composition 3 afforded lower D s and required longer development times than did composition 1.
- EXAMPLE 10 The negative image prepared in Example 5 was subjected to accelerated tests for stability to light, heat and humidity (ultraviolet lamp for 72 hours; relative humidity at F. for 40 hours; 80% relative humidity at F. for 16 hours in the presence of powdered sulfur), and was found to be exceptionally stable although perhaps not of archival stability.
- a fully developed and fixed negative prepared as described in Example 1 has been found to be stable, e.g., no density fading and density increase in highlights, when stored at room temperature and humidity for over two years.
- a photographic process comprising the steps of contacting an exposed light-sensitive silver halide emulsion containing a developable image with an aqueous alkaline processing composition having a pH above 10.5 and including a silver halide solvent, a high energy aminophenol silver halide developing agent containing in a position ortho to the phenolic hydroxyl group at least one substituent selected from the group consisting of amino, lower alkyl and lower alkoxy groups and a low-energy silver halide developing agent selected from the group consisting of ascorbic acids and hydroxylamines, said low-energy developing agent being present in substantially greater concentration than said high-energy developing agent, the amount of each of said low-energy and high-energy developing agents alone being insuflicient to develop appreciable negative density, but said respective amounts together providing a synergistic effect whereby said combined developing agents are capable of developing exposed silver halide to a desired usable density;
- a process as defined in claim 1 wherein said highenergy silver halide developing agent is 4-amino-2,6-dimethyl-phenol and said low-energy silver halide developing agent is isoascorbic acid.
- a photographic processing composition for use in processes for forming silver transfer images comprising an aqueous alkaline solution containing a silver halide solvent, a high-energy aminophenol silver halide developing agent containing in a position ortho to the phenolic hydroxyl group at least one substituent selected from the group consisting of amino, lower alkyl and lower alkoxy groups and a low-energy silver halide developing agent selected from the group consisting of ascorbic acids and hydroxyl amines, said low-energy developing agent being present in substantially greater concentration than said high-energy developing agent, the amount of each of said low-energy and high-energy silver halide developing agent alone being insufiicient to develop appreciable negative density, but said respective amounts together providing a synergistic effect whereby said combined developing agents are capable of developing exposed silver halide to a desired usable density, said processing composition having a pH above 10.5.
- composition as defined in claim 9 wherein the pH of said composition is between 10.5 and about 12.5.
- composition as defined in claim 9 wherein said high-energy silver halide developing agent is 2,4-diaminoortho-cresol.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US43804465A | 1965-03-08 | 1965-03-08 | |
US69072867A | 1967-12-15 | 1967-12-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3549364A true US3549364A (en) | 1970-12-22 |
Family
ID=27031523
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US690728A Expired - Lifetime US3549364A (en) | 1965-03-08 | 1967-12-15 | Photographic processes and compositions |
Country Status (2)
Country | Link |
---|---|
US (1) | US3549364A (fr) |
NL (1) | NL6602944A (fr) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3723117A (en) * | 1969-10-27 | 1973-03-27 | Agfa Gevaert | Method for developing silver halide emulsions |
EP0476613A2 (fr) * | 1990-09-19 | 1992-03-25 | Dainippon Ink And Chemicals, Inc. | Procédé pour former des images négatives à très haut contraste |
US5399457A (en) * | 1993-10-15 | 1995-03-21 | Minnesota Mining And Manufacturing Company | Process for reducing sludge in diffusion transfer printing plates |
WO2004001504A1 (fr) * | 2002-05-15 | 2003-12-31 | Dianne Iverglynne | Solution de developpement biodegradable et son procede d'utilisation |
FR3076214A1 (fr) * | 2017-12-28 | 2019-07-05 | L'oreal | Procede de coloration d'oxydation mettant en œuvre un substrat portant au moins un colorant d'oxydation, plusieurs conservateurs, et une composition aqueuse oxydante |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2060596A (en) * | 1934-06-09 | 1936-11-10 | Agfa Ansco Corp | Photographic developer |
US2857276A (en) * | 1954-11-23 | 1958-10-21 | Polaroid Corp | Photographic processes and compositions useful therein |
US3022168A (en) * | 1958-06-28 | 1962-02-20 | Pharmacia Ab | Photographic developer |
US3041170A (en) * | 1959-10-29 | 1962-06-26 | Eastman Kodak Co | New class of development promoter precursors for dry processing self-developing silver halide coatings |
US3134673A (en) * | 1960-02-19 | 1964-05-26 | Ilford Ltd | Photographic developers |
-
1966
- 1966-03-07 NL NL6602944A patent/NL6602944A/xx unknown
-
1967
- 1967-12-15 US US690728A patent/US3549364A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2060596A (en) * | 1934-06-09 | 1936-11-10 | Agfa Ansco Corp | Photographic developer |
US2857276A (en) * | 1954-11-23 | 1958-10-21 | Polaroid Corp | Photographic processes and compositions useful therein |
US3022168A (en) * | 1958-06-28 | 1962-02-20 | Pharmacia Ab | Photographic developer |
US3041170A (en) * | 1959-10-29 | 1962-06-26 | Eastman Kodak Co | New class of development promoter precursors for dry processing self-developing silver halide coatings |
US3134673A (en) * | 1960-02-19 | 1964-05-26 | Ilford Ltd | Photographic developers |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3723117A (en) * | 1969-10-27 | 1973-03-27 | Agfa Gevaert | Method for developing silver halide emulsions |
EP0476613A2 (fr) * | 1990-09-19 | 1992-03-25 | Dainippon Ink And Chemicals, Inc. | Procédé pour former des images négatives à très haut contraste |
EP0476613A3 (en) * | 1990-09-19 | 1992-06-03 | Dainippon Ink And Chemicals, Inc. | Superhigh contrast negative image forming process |
US5217842A (en) * | 1990-09-19 | 1993-06-08 | Dainippon Ink And Chemical, Inc. | Superhigh contrast negative image forming process |
US5399457A (en) * | 1993-10-15 | 1995-03-21 | Minnesota Mining And Manufacturing Company | Process for reducing sludge in diffusion transfer printing plates |
EP0649062A2 (fr) * | 1993-10-15 | 1995-04-19 | Minnesota Mining And Manufacturing Company | Procédé pour réduire la formation de boue dans des plaques d'impression pour le procédé de diffusion-transfert |
EP0649062A3 (fr) * | 1993-10-15 | 1995-08-16 | Minnesota Mining & Mfg | Procédé pour réduire la formation de boue dans des plaques d'impression pour le procédé de diffusion-transfert. |
WO2004001504A1 (fr) * | 2002-05-15 | 2003-12-31 | Dianne Iverglynne | Solution de developpement biodegradable et son procede d'utilisation |
FR3076214A1 (fr) * | 2017-12-28 | 2019-07-05 | L'oreal | Procede de coloration d'oxydation mettant en œuvre un substrat portant au moins un colorant d'oxydation, plusieurs conservateurs, et une composition aqueuse oxydante |
Also Published As
Publication number | Publication date |
---|---|
NL6602944A (fr) | 1966-09-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2592368A (en) | Gelatine silver halide emulsion layer containing a dihydroxy diphenyl tanning developing agent | |
US2647056A (en) | One step photographic transfer process | |
US2500421A (en) | Photographic silver halide transfer process | |
US2635048A (en) | Photographic transfer product and process | |
GB714412A (en) | Improvements in or relating to photographic process and agent | |
US2725298A (en) | Transfer process of photographic printing | |
GB454622A (en) | Improvements in colour photography | |
US3549364A (en) | Photographic processes and compositions | |
US3087816A (en) | Photographic diffusion transfer process | |
US3769014A (en) | Beta-disulfone silver halide solubilizing agents | |
US2449153A (en) | Photographic silver bromide emulsion sensitized with cysteine | |
GB687751A (en) | Process and material for the direct production of positive photographic images | |
US3189454A (en) | Method of photographic development and fixing | |
US3721562A (en) | Integral laminate photographic units comprising developing composition-spreader sheets containing a polymeric acidifying layer | |
US3740221A (en) | Development of photographic material | |
US3265502A (en) | Photographic developing compositions | |
US3265501A (en) | Water-swellable colloidal magnesium aluminum silicate photographic composition | |
GB800772A (en) | Improvements in processes of photographic reproduction | |
US3343958A (en) | Monobath containing cysteine-nitrogenous base combination | |
US3515555A (en) | Toning composition for direct positive paper | |
US3640713A (en) | Photographic processes and compositions therefor | |
US2939788A (en) | Novel photographic developers | |
US2984565A (en) | Photographic process and composition | |
US3563740A (en) | Use of dicyanamides in and with photosensitive systems | |
US3620728A (en) | Receiving sheet for diffusion transfer processes |