US2419900A - Bleaching bath and process for bleaching color film - Google Patents
Bleaching bath and process for bleaching color film Download PDFInfo
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- US2419900A US2419900A US627527A US62752745A US2419900A US 2419900 A US2419900 A US 2419900A US 627527 A US627527 A US 627527A US 62752745 A US62752745 A US 62752745A US 2419900 A US2419900 A US 2419900A
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- bleaching
- silver
- color
- film
- bath
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- 238000004061 bleaching Methods 0.000 title description 36
- 238000000034 method Methods 0.000 title description 30
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 31
- 229910052709 silver Inorganic materials 0.000 description 31
- 239000004332 silver Substances 0.000 description 31
- 239000000243 solution Substances 0.000 description 20
- 239000000839 emulsion Substances 0.000 description 13
- 239000007844 bleaching agent Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 125000000217 alkyl group Chemical group 0.000 description 10
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 10
- 239000007800 oxidant agent Substances 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 238000009792 diffusion process Methods 0.000 description 7
- JYINMLPNDRBKKZ-UHFFFAOYSA-N hydroperoxybenzene Chemical compound OOC1=CC=CC=C1 JYINMLPNDRBKKZ-UHFFFAOYSA-N 0.000 description 7
- 229960005323 phenoxyethanol Drugs 0.000 description 7
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 7
- 239000000975 dye Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- 150000002431 hydrogen Chemical class 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- -1 bromine or chlorine Chemical class 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000875 corresponding effect Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 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 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- OIDPCXKPHYRNKH-UHFFFAOYSA-J chrome alum Chemical compound [K]OS(=O)(=O)O[Cr]1OS(=O)(=O)O1 OIDPCXKPHYRNKH-UHFFFAOYSA-J 0.000 description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 2
- 229910000397 disodium phosphate Inorganic materials 0.000 description 2
- 235000019800 disodium phosphate Nutrition 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- 235000010265 sodium sulphite Nutrition 0.000 description 2
- QNGVNLMMEQUVQK-UHFFFAOYSA-N 4-n,4-n-diethylbenzene-1,4-diamine Chemical compound CCN(CC)C1=CC=C(N)C=C1 QNGVNLMMEQUVQK-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 101150097504 LHX1 gene Proteins 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910000318 alkali metal phosphate Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- YAGKRVSRTSUGEY-UHFFFAOYSA-N ferricyanide Chemical compound [Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] YAGKRVSRTSUGEY-UHFFFAOYSA-N 0.000 description 1
- TVHALOSDPLTTSR-UHFFFAOYSA-H hexasodium;[oxido-[oxido(phosphonatooxy)phosphoryl]oxyphosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O TVHALOSDPLTTSR-UHFFFAOYSA-H 0.000 description 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 101150031270 mak-1 gene Proteins 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- RHUVFRWZKMEWNS-UHFFFAOYSA-M silver thiocyanate Chemical compound [Ag+].[S-]C#N RHUVFRWZKMEWNS-UHFFFAOYSA-M 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
- 239000000126 substance Substances 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
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/42—Bleach-fixing or agents therefor ; Desilvering processes
- G03C7/421—Additives other than bleaching or fixing agents
Definitions
- This invention relates to photographic bleaching baths, to such baths employed in multicolor photography, and especially to baths for the bleaching of the silver image in a multicolor film following color-forming development.
- An object of the present invention is to provide solutions for the removal of metallic silver from multicolored photographic layers.
- a further object is to provide a method and wherein R is an alkyl group, such as methyl, ethyl, propyl, and the like, X represents either hydrogen, an alkyl of the same value as R or a halogen, such as bromine or chlorine, and n represents a positive integer of from 1 to 3.
- R is an alkyl group, such as methyl, ethyl, propyl, and the like
- X represents either hydrogen, an alkyl of the same value as R or a halogen, such as bromine or chlorine
- n represents a positive integer of from 1 to 3.
- the concentration of the phenoxy alcohol required may vary considerably. For instance, as little as 5 grams per liter of bleach solution has been found to effect the complete conversion of metallic silver into a silver-salt soluble in the usual silver-salt solvent, and as much as 20 grams per liter can be used without interference with the properties of the bleaching solution. Amounts higher than 20 grams per liter can be employed, but the concentration actually employed should not exceed the solubility limits of the alcohol selected. For practical purposes, however, concentrations ranging from between 5 and 15 grams per liter are most desirable. 'I'hese alcohols are readily removed in the subsequent washing of the film and do not leave oily slicks on the surface, nor do they effect the film base in any way.
- a typical bleach solution consists of grams of an oxidizing agent per liter of solution, and may contain one or more of the following ingredients:
- Potassium bromide By an oxidizing agent I mean an inorganic chemical compound that will oxidize a metallic silver image to form a silver-salt. Most commonly used oxidizing agents are alkali metal ferricyanides, such as sodium, potassium, ammonium ferricyanides, the alkali metal persulfates, i. e., the sodium and potassium persulfates, or mixtures of these salts.
- a converting agent I mean a chemical compound such as potassium bromide or sodium thiocyanate which by reason of a difierence in solubility will replace the silver ferrocyanide formed in the bleaching reaction (when ferricyanide is used as the oxidizing agent) to form silver bromide or silver thiocyanate and thus impel the bleaching reaction to go to completion.
- Converting agents are sometimes called halogenizing agents.
- buflering agents I mean any substance that is added to bring the bleach solution to a. specified pH and to maintain this pI-I even though small amounts of acids or alkali may be carried into the bleach by the film.
- the pHs used in bleaching color films are generally maintained between 3 and 9.
- corrosion preventive I refer to those compounds which retard the corrosive effect of the bleach solution on developing tanks, trays, etc.
- alkali metal phosphates such as disodium phosphate, sodium tetraphosphate, and the like, have been found to do this effectively as well as dialkyl amino alcohols as described in United States Patent 2,327,813.
- solvent I refers to the liquid in which the above materials are dissolved which is usually water.
- Example I Two exposed 4 x 5" multilayer color film sheets, of the Ansco Color Film reversal type and containing color-formers fast to diffusion, were processed as follows:
- the first washed film was treated in solution No. 1 and the second washed film was treated in solution No. 2 of the following compositions:
- the two bleached film sheets were then washed in water for minutes, fixed for 5 minutes in a 20% aqueous hypo solution, washed for an additional 5 minutes and then dried.
- the film bleached in solution No. 1 showed objectionable haziness due to the presence of metallic silver in the layers, whereas the film bleached in solution No. 2 containing B-phenoxyethanol was clear and of the desired color rendition.
- the first washed film was treated in solution
- the two bleached sheet films were then washed for 5 minutes, fixed for 5 minutes in a 20% aqueous solution of hypo, washed an additional minutes and then dried.
- the film bleached in solution No. 1 containing no l-(p-bromophenoxy) -propanol-2 showed considerable haziness, whereas the film bleached in solution No. 2 was clear and of the desired color rendition.
- Example I [1 Example I was repeated with the exception that the bleach bath No. 2 contained 10 grams of s-phenoxypropanol instead of ,a-phenoxyethanol. The film bleached in the solution containing no ,i-phenoxypropanol showed objectionable haziness, while the film bleached with the solution containing e-phenoxy-propanol was clear and of the desired color rendition.
- R is alkyl
- X is a member selected from the class consisting of hydrogen, alkyl, and halogen
- n is a positive integer of from 1 to 3.
- R is alkyl
- X is a member selected from the class consisting of hydrogen, alkyl, and halogen
- n is a positive integer of from 1 to 3.
- a photographic bleaching bath comprising an aqueous solution of an inorganic oxidizing agent and a phenoxy alcohol selected from the class consisting of those corresponding to the following formulae:
- a photographic bleaching bath comprising an aqueous solution of an inorganic oxidizing agent and fi-phenoxyethanol.
- a photographic bleaching bath comprising an aqueous solution of an inorganic oxidizing agent and l-(p-methylphenoxy)-propanol-2.
- a photographic bleaching bath comprising an aqueous solution of an inorganic oxidizing agent and c-phenoxypropanol.
- R is alkyl
- X is a member selected from the class consisting of hydrogen, alkyl, and halogen
- n is a positive integer of from 1 to 3.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Description
Be ti/999W") Search Root Patented Apr. 29, 1947 BLEACHING BATH AND PROCESS FOR BLEACHING COLOR FILM Frank J. Kaszuba, Binghamton, N. Y., assignor to General Aniline & Film Corporation, New York, N. Y., a corporation of Delaware No Drawing. Application November 8, 1945, Serial No. 627,527
17 Claims.
This invention relates to photographic bleaching baths, to such baths employed in multicolor photography, and especially to baths for the bleaching of the silver image in a multicolor film following color-forming development.
It is known that in the processing of multicolor reversal film and multicolor negative film, the silver present in all the layers following development is converted into a salt by any of the well-known silver-salt formers, commonly known as bleaching baths, and the silver-salt thus formed is then removed by dissolving it in a silversalt solvent such as, for example, hypo. In certain color photographic emulsions containing an organic solvent for color-couplers, such as a water-insoluble but water permeable cellulose binder or a high-boiling crystalloidal material as described in United States Patents 2,304,940 and 2,322,027, respectively, there is a tendency for these solvents to occlude the metallic silver following development and to prevent its conversion into a silver salt by the customary bleaching bath. In the processes described in these patents, the coupler originally present in the emulsion layer and the dye formed from it are dissolved in globules of the organic solvent which traps or wets the particles of metallic silver as it is formed during the development step and then encloses portions of it which can no longer be affected by the bleaching bath. In order to obviate this diificulty, it has been proposed in United States Patent 2,378,265 to incorporate into a bleach bath an organic solvent such as a monohydroxy alcohol or an aliphatic ketone. These solvents permit the bleach bath to penetrate any organic material in the emulsion so that the bleach bath is able to act on the metallic silver formed therein during development.
It has been found that in removing metallic silver from multicolor photographic layers, which are prepared by the direct dispersion of colorformers fast to diffusion in silver-halide emulsions as disclosed in United States Patents means for the complete removal of metallic silver from silver-halide emulsion layers containing dispersed color-formers fast to diffusion.
Other objects and features of the invention will become apparent as the description proceeds.
I have found that the above objects are accomplished by incorporating into a bleach solution commonly known and used in color photography,. a phenoxy alcohol represented by the following general formulae:
(I)(CH2)nOH and o-orucn-n 2,179,228: 2,l79,2389; 2,179,234; 2,178,612; 2,179.244; 2,186.719; 2.l86,8512; 2,186,732-3-4: 2,186,849; 2,186,045; 2,200,306; 2,280,722; 2,292,575; 2.303928; and 2,307,399, bleaching in which it is located with the result that even the poor color rendition is finally obliterated.
An object of the present invention is to provide solutions for the removal of metallic silver from multicolored photographic layers.
A further object is to provide a method and wherein R is an alkyl group, such as methyl, ethyl, propyl, and the like, X represents either hydrogen, an alkyl of the same value as R or a halogen, such as bromine or chlorine, and n represents a positive integer of from 1 to 3.
This discovery makes it possible to enable the bleach bath to oxidize all of the metallic silver in the developed color film, and to permit its complete removal from the photographic layers. Furthermore, it has been found that such alcohols may be utilized in the bleaching of silver from any color film whether the dyestuff images be formed while employing the color-formers in the layer or while forming the dyestufi images by the methods known as the controlled diffusion method or the selected second exposure and color development method, as disclosed in United States Patents 1,897,866; 1,900,870; 1,928,709 and 1,980,941. In the latter cases, better results are often achieved when using bleaching baths containing these alcohols than when using the monohydroxy alcohols and aliphatic ketones referred to in United States Patert 2,378,265. The invention is accordingly generic to the removal of silver from any photographic color film where the dyestufi images are produced by colorforming development.
The concentration of the phenoxy alcohol required may vary considerably. For instance, as little as 5 grams per liter of bleach solution has been found to effect the complete conversion of metallic silver into a silver-salt soluble in the usual silver-salt solvent, and as much as 20 grams per liter can be used without interference with the properties of the bleaching solution. Amounts higher than 20 grams per liter can be employed, but the concentration actually employed should not exceed the solubility limits of the alcohol selected. For practical purposes, however, concentrations ranging from between 5 and 15 grams per liter are most desirable. 'I'hese alcohols are readily removed in the subsequent washing of the film and do not leave oily slicks on the surface, nor do they effect the film base in any way.
The following are examples of phencxy alcohols employed in accordance with the present invention:
OCH2.CH2OH B-phenoxyetlmnol fl-(p-chloropheuoxy) ethanol (3) OCH.CH.CH:
l-(p-methylphenoxy)-propanol-2 (4) O-GHaCHsOH OCH:.CH.CH:
l-plieuoxy propanol-2 0CHz.CHlCHi 1-(p-bromophenoxy)-propsnol-2 0-CHz-CHICH1OH B-phenoxypropenol vent, such as, for example, water, with or without the presence of other adjuvants. A typical bleach solution consists of grams of an oxidizing agent per liter of solution, and may contain one or more of the following ingredients:
Potassium bromide (converting agent) By an oxidizing agent I mean an inorganic chemical compound that will oxidize a metallic silver image to form a silver-salt. Most commonly used oxidizing agents are alkali metal ferricyanides, such as sodium, potassium, ammonium ferricyanides, the alkali metal persulfates, i. e., the sodium and potassium persulfates, or mixtures of these salts.
By a converting agent I mean a chemical compound such as potassium bromide or sodium thiocyanate which by reason of a difierence in solubility will replace the silver ferrocyanide formed in the bleaching reaction (when ferricyanide is used as the oxidizing agent) to form silver bromide or silver thiocyanate and thus impel the bleaching reaction to go to completion. Converting agents are sometimes called halogenizing agents.
By buflering agents I mean any substance that is added to bring the bleach solution to a. specified pH and to maintain this pI-I even though small amounts of acids or alkali may be carried into the bleach by the film. The pHs used in bleaching color films are generally maintained between 3 and 9.
By corrosion preventive I refer to those compounds which retard the corrosive effect of the bleach solution on developing tanks, trays, etc. Large quantities (20-80 grams per liter) of alkali metal phosphates such as disodium phosphate, sodium tetraphosphate, and the like, have been found to do this effectively as well as dialkyl amino alcohols as described in United States Patent 2,327,813.
By solvent I refer to the liquid in which the above materials are dissolved which is usually water.
The following examples describe in detail methods for accomplishing the above objects, but it is to be understood that they are inserted merely for purposes of illustration and are not to be construed as limiting the scope of the invention.
Example I Two exposed 4 x 5" multilayer color film sheets, of the Ansco Color Film reversal type and containing color-formers fast to diffusion, were processed as follows:
First development for 10 minutes at 68 F. in a developer of the following composition:
Short stopped for 3 minutes in a 3% aqueous solution of acetic acid.
Washed for 2 minutes in running water.
Second exposure for 3 minutes to light of a No. 1 photo-flood lamp 30 inches away from the film.
Color development for 15 inmutes in a developer of the following composition:
Sodium sulfite grams 5 p-Amino diethyl aniline HCl do 4 Sodium carbonate do 40 Potassium bromide do 1 Water to make up liter 1 Rinsed for 1 minute in running water.
Hardened for 5 minutes in a 3% aqueous solution of chrome alum.
Washed for 5 minutes in running water.
The first washed film was treated in solution No. 1 and the second washed film was treated in solution No. 2 of the following compositions:
No. l .\'o. 2
Disodium monopotassiuni fon'icyaniriu grams. 1H0 100 Potassium bromide. (UL ml 10 Sodium tetraphosphatc. 20 20 Disodium pho phate .7 40 Sodium bisulfite.. r 25 25 B-phenoxyethanoL v l0 Water to mak1. .up lim- 1 l The two bleached film sheets were then washed in water for minutes, fixed for 5 minutes in a 20% aqueous hypo solution, washed for an additional 5 minutes and then dried. The film bleached in solution No. 1 showed objectionable haziness due to the presence of metallic silver in the layers, whereas the film bleached in solution No. 2 containing B-phenoxyethanol was clear and of the desired color rendition.
Example [I Two exposed 4" x 5" multilayer color film sheets of Ansco Color" negative film and containing color-formers fast to diffusion were processed as follows:
Developed for minutes at 68 F. in a developer of the following composition:
Sodium sulfite grams 0.5 2 amino-5-diethylarninotoluene hydrochloride do 2.5 Hydroxylamine HCl do 1 Sodium carbonate d0 65 Potassium bromide d0 2.5 Water to make up liter- 1 Short stopped for 5 minutes in a solution of the following composition:
Monopotassium phosphate grams 80 Disodium phosphate do 20 Water to make up liter 1 Hardened for 3 minutes in a 3% chrome alum solution.
Washed for 5 minutes in running Water.
The first washed film was treated in solution The two bleached sheet films were then washed for 5 minutes, fixed for 5 minutes in a 20% aqueous solution of hypo, washed an additional minutes and then dried. As in Example I, the film bleached in solution No. 1, containing no l-(p-bromophenoxy) -propanol-2 showed considerable haziness, whereas the film bleached in solution No. 2 was clear and of the desired color rendition.
Example I [1 Example I was repeated with the exception that the bleach bath No. 2 contained 10 grams of s-phenoxypropanol instead of ,a-phenoxyethanol. The film bleached in the solution containing no ,i-phenoxypropanol showed objectionable haziness, while the film bleached with the solution containing e-phenoxy-propanol was clear and of the desired color rendition.
The above specific examples are to be regarded as merely illustrative of the invention, and not in any sense restrictive. It will be obvious to anyone skilled in the art that many modifications such as substituting equivalent materials and varying the proportions of materials used are within the spirit and scope of the invention as defined in the appended claims.
I claim:
1. In a process of color photography the method of removing silver from the film after dyestuff image formation by the action of a bleaching bath which comprises treating said film with such a bath containing a phenoxy alcohol selected from the class consisting of those corresponding to the following formulae:
and
(]) CH2CHR wherein R is alkyl, X is a member selected from the class consisting of hydrogen, alkyl, and halogen, and n is a positive integer of from 1 to 3.
2. In a process of color photography the method of removing silver from a color film containing dyestuff images which are produced by color-forming development of an emulsion containing a dyestuff former fast to diffusion, the improvement which comprises subjecting said film to the action of a bleaching bath containing a phenoxy alcohol selected from the class consisting of those corresponding to the following formulae:
wherein R is alkyl, X is a member selected from the class consisting of hydrogen, alkyl, and halogen, and n is a positive integer of from 1 to 3.
3. In a process of cOlOr photography the method of removing silver from a color film containing dyestufi images which are produced by colorforming development of an emulsion containing a dyestufl former fast to difiusion, the improvement which comprises subjecting said film to the action of a bleaching bath containing ,B-phenoxyethanol.
4. In a process of color photography the method of removing silver from a color film containing dyestuif images which are produced by colorforming development of an emulsion containing a dyestuiT former fast to diffusion, the improvement which comprises subjecting said film to the action of a bleaching bath containing l-(p-methylphenoxy) -propanol-2.
5. In a process of color photography the method of removing silver from a color film containing dyestuff images Which are produced by colorforming development of an emulsion containing a dyestufi former fast to difiusion, the improvement which comprises subjecting said film to the action of a bleaching bath containing fi-phenoxypropanol.
6. In a process of color photography the method of removing silver by the action of a bleaching bath which comprises adding to said bath 5- phenoxyethanol.
'7. In a process of color photography the meth- 0d of removing silver by the action of a bleaching bath which comprises adding to said bath 1- (p-methylphenoxy) -propanol-2.
8. In a process of color photography the meth- 0d of removing silver by the action of a bleaching bath which comprises adding to said bath 5- phenoxypropanol.
9. The method according to claim 1 wherein the concentration of the phenoxy alcohol ranges from 5 to 20 grams per liter of bleach.
10. A photographic bleaching bath comprising an aqueous solution of an inorganic oxidizing agent and a phenoxy alcohol selected from the class consisting of those corresponding to the following formulae:
. Q-(CHzMOH.
and
(|)CH:CH--R wherein R is alkyl, X is a member selected from the class consisting of hydrogen, alkyl, and halogen, and n is a positive integer of from 1 to 3.
11. A photographic bleaching bath comprising an aqueous solution of an inorganic oxidizing agent and fi-phenoxyethanol.
12. A photographic bleaching bath comprising an aqueous solution of an inorganic oxidizing agent and l-(p-methylphenoxy)-propanol-2.
13. A photographic bleaching bath comprising an aqueous solution of an inorganic oxidizing agent and c-phenoxypropanol.
14. In a process of producing photographic color images in a silver-halide emulsion by colorforming development in which silver images produced in the process are removed by the action of a bleaching bath applied subsequent to the color development step, the improvement which comprises removing the silver by the action of a bleaching bath containing a phenoxy alcohol selected from the class consisting of those corre sponding to the following formulae:
wherein R is alkyl, X is a member selected from the class consisting of hydrogen, alkyl, and halogen, and n is a positive integer of from 1 to 3.
15. In a process of producing photographic color images in a silver-halide emulsion by colorforming development in which silver images produced in the process are removed by the action of a bleaching bath applied subsequent to the color development step, the improvement which comprises removing silver by the action of a bleaching bath containing p-phenoxyethanol.
16. In a process of producing photographic color images in a silver-halide emulsion by colorforming development in which silver images produced in the process are removed by the action of a bleaching bath applied subsequent to the color development step, the improvement which comprises removing silver by the action of a bleaching bath containing 1-(p-methylphenoxy) -propanol-2.
17. In a process of producing photographic color images in a silver-halide emulsion by colorforming development in which silver images produced in the process are removed by the action of a bleaching bath applied subsequent to the color development step, the improvement which comprises removing silver by the action of a bleaching bath containing B-phenoxypropanol.
FRANK J. KASZUBA.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22977D USRE22977E (en) | 1945-11-08 | Bleaching bath and process for | |
| US627527A US2419900A (en) | 1945-11-08 | 1945-11-08 | Bleaching bath and process for bleaching color film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US627527A US2419900A (en) | 1945-11-08 | 1945-11-08 | Bleaching bath and process for bleaching color film |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2419900A true US2419900A (en) | 1947-04-29 |
Family
ID=24515022
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US22977D Expired USRE22977E (en) | 1945-11-08 | Bleaching bath and process for | |
| US627527A Expired - Lifetime US2419900A (en) | 1945-11-08 | 1945-11-08 | Bleaching bath and process for bleaching color film |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US22977D Expired USRE22977E (en) | 1945-11-08 | Bleaching bath and process for |
Country Status (1)
| Country | Link |
|---|---|
| US (2) | US2419900A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1062114B (en) * | 1957-05-15 | 1959-07-23 | Gen Aniline & Film Corp | Stable photographic bleach |
| US3042520A (en) * | 1959-04-23 | 1962-07-03 | Gen Aniline & Film Corp | Bleaching bath for processing color film |
-
0
- US US22977D patent/USRE22977E/en not_active Expired
-
1945
- 1945-11-08 US US627527A patent/US2419900A/en not_active Expired - Lifetime
Non-Patent Citations (1)
| Title |
|---|
| None * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1062114B (en) * | 1957-05-15 | 1959-07-23 | Gen Aniline & Film Corp | Stable photographic bleach |
| US3042520A (en) * | 1959-04-23 | 1962-07-03 | Gen Aniline & Film Corp | Bleaching bath for processing color film |
Also Published As
| Publication number | Publication date |
|---|---|
| USRE22977E (en) | 1948-02-24 |
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