US2983607A - Tetramethylolcyclohexanol treatment to trevent popping and fading of transparencies and fading of color prints - Google Patents
Tetramethylolcyclohexanol treatment to trevent popping and fading of transparencies and fading of color prints Download PDFInfo
- Publication number
- US2983607A US2983607A US788765A US78876559A US2983607A US 2983607 A US2983607 A US 2983607A US 788765 A US788765 A US 788765A US 78876559 A US78876559 A US 78876559A US 2983607 A US2983607 A US 2983607A
- Authority
- US
- United States
- Prior art keywords
- transparencies
- fading
- color
- tetramethylolcyclohexanol
- popping
- 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
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- SQHKJSPPFSVNDF-UHFFFAOYSA-N 1,2,2,3-tetrakis(hydroxymethyl)cyclohexan-1-ol Chemical compound OCC1CCCC(O)(CO)C1(CO)CO SQHKJSPPFSVNDF-UHFFFAOYSA-N 0.000 title description 9
- 238000011282 treatment Methods 0.000 title description 8
- 238000005562 fading Methods 0.000 title description 4
- 238000000034 method Methods 0.000 claims description 9
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 150000001923 cyclic compounds Chemical class 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000007788 liquid Substances 0.000 description 8
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 6
- 230000006866 deterioration Effects 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 229910052709 silver Inorganic materials 0.000 description 4
- 239000004332 silver Substances 0.000 description 4
- -1 silver halide Chemical class 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 229940051250 hexylene glycol Drugs 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229920006324 polyoxymethylene Polymers 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- SMZMEQKOUTVGJO-UHFFFAOYSA-N 2,2,3,3-tetrakis(hydroxymethyl)cyclohexan-1-one Chemical compound OCC1(CO)CCCC(=O)C1(CO)CO SMZMEQKOUTVGJO-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 229940093475 2-ethoxyethanol Drugs 0.000 description 1
- SXFJDZNJHVPHPH-UHFFFAOYSA-N 3-methylpentane-1,5-diol Chemical compound OCCC(C)CCO SXFJDZNJHVPHPH-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 238000004383 yellowing 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
- G03C11/00—Auxiliary processes in photography
-
- 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
- G03C5/268—Processing baths not provided for elsewhere, e.g. pre-treatment, stop, intermediate or rinse baths
-
- 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
- G03C7/3046—Processing baths not provided for elsewhere, e.g. final or intermediate washings
Definitions
- This invention concerns the treatment of colored photographs, more particularly to a final rinse bath to stabilize the dyes present in the image layers.
- a problem peculiar to transparent photographic elements is that of avoiding popping of colored photographic transparencies during optical projection. Popping is a characteristic of most transparencies which occurs when the transparency is placed in the slide changer through which the light is transmitted. Due to the heat, the transparency buckles with a resulting change in focus which necessitates refocusing. Many solutions have been suggested for the problem, including lacquering the transparency, redesigning the projector to provide a cooled light, and the like. However, it has been desirable to find a simple treatment for the transparencies which will prevent them from popping without deleteriously effecting the transparency itself.
- One object of this invention is to provide a method of stabilizing the colors in colored photographs. Another object is to provide stabilized colored transparencies which can be projected optically without popping. A further object is to provide a simple method of after-treatment for colored photographic elements which will stabilize the colors against deterioration or alteration.
- the above objects are obtained by treatment of the photographic elements with an aqueous solution containing 520% by weight of a tetramethylol cyclic alcohol or ketone having 5-8 carbon atoms in the ring.
- the photographic element whether a print, a transparency or a negative is dipped in the bath of the cyclic alcohol or ketone for 1-10 minutes, although this period is not critical.
- Surplus liquid can be removed with a squeegee, rapid water wash or other means.
- the photographic element may then be dried at room temperature or more rapidly in an oven.
- a polymethylene glycol having from 4 to 8 carbon 5 atoms such as 2-methylpentane-2,4-diol may be added as a plasticizer in the treatment bath at a concentration of about 2-3% by weight.
- Other polymet'hylene glycols which may be used include hexyleneglycol, hexamethy1ene-l,6-diol, 3-methylpentane-1,5-diol, tetrarnethylene-l,4-diol, Z-ethoxyethanol and the like.
- Example 1 Fully processed colored transparencies of the type described in 11.8.
- Patent 2,304,939 containing three layers of light-sensitive emulsion, each layer being sensitive to a particular color, such as the blue-sensitive silver halide layer, green-sensitive silver halide layer, and red-sensitive silver halide layer were dipped in a solution of 8% tetramethylol cyclohexanol and 2% 2-methylpentaue2,4-diol for 2 minutes, squeegeed and dried at room temperature.
- These transparencies did not pop in a Kodaslide projector with a 250-watt lamp during 3 minutes. An untreated slide popped within 15 seconds.
- Slides were also treated with 5, 10, 15 and 20% solutions of tetramethylolcyclohexanol, and with mixtures of 5%+2%, 10%+2%, 15%+2% and 10%+2.5% con centrations of tetramethylolcyclohexanol and 2-rnethylpentane-2,4-diol. None of the slides treated popped during 1 /2 minutes.
- Example 2 Color transparencies of the type described in Example 1 were fully processed and washed. These transparencies were immersed in an aqueous solution of tetramethylolcyclohexanol for 10 minutes, squeegeed and dried. Together with a water-washed slide they were exposed to light from a SOD-watt tungsten filament lamp at a distance of 8.5 inches for hours in a Fadorneter, and at the same time cooled by a current of air blown through the Fadometer. The following table gives the approximate percentage loss of density (from an original density of 1.0) for the yellow and magenta images.
- the cyan dye Example Color prints prepared according to US. Patent 2,272,191, were processed, washed, and immersed for 10 minutes in an aqueous solution of tetramethylolcyclohexanol. The prints were squeegeed and dried. To-
- Example 4 Color transparencies of the type described in Example 1 are immersed in a 7.5% solution of 2:2:52S-tetramethylolcyclopentanone in water for 10 minutes, then removed from the solution, surplus liquid squeegeed oil, and dried.
- Example 5 Color transparencies of the type described in Example 1 are immersed in a 7.5% solution of 2:2:6z6-tetramethylolcyclohexanone in water for minutes, then removed from the solution, surplus liquid squeegeed off, and dried.
- Example 6 Color prints of the type of Example 3 are immersed in a 10% solution of 2:2:5:S-tetramethylolcyclopentanone in water for 10 minutes, then removed from the solution, surplus squeegeed oh, and dried.
- Example 7 Color prints of the type of Example 3 are immersed in a 10% solution of 2:2:6:6rtetramethylolcyclohexanone in water for 10 minutes, then removed from the solution, surplus liquid squeegeed off, and dried.
- Example 8 Color transparencies of the type described in Example 1 are immersed in an 8% solution of 2:2:6z6-tetramethylolcyclohexanol and 2% of 2-ethoxyethanol in water for 10 minutes, then removed from the solution, surplus liquid squeegeed off, and dried.
- Example 9 Color transparencies of the type described in Example l are immersed in an 8% solution of 2:216:6-tetramethylolcyclohexanol and 2% tetramethylene-1z4-diol in water for 10 minutes, then removed from. the solution, surplus liquid squeegeed off, and dried.
- Example 10 Color transparencies of the type described in Example 1 are immersed in a 10% solution of a mixture of 3- methyland 4-methyl-2: 2: 6 6-tetramethylolcyclohexanol in water for 10 minutes, then removed from the solution, surplus liquid squeegeed 011?, and dried.
- Example 11 Color transparencies of the type described in Example 1 are immersed in an aqueous solution of 8% 2:2:6z6-
- Photographic colored elements which are operative in our invention include those-illustrated in the examples as well as those disclosed in U.S. Patent 2,296,306. They also include color positive print material coated on paper in which the color formers are present in the emulsion or are obtained using a selective second exposure'followed by development by developing solutions containing color formers and color developing agents. Other color elements include color reversible film, color negative film, and color reversible white printing mate: rial coated on an opaque base. M v 4 An example .of. a developing. process for colored photographic elements known as the E2 Process is disclosed in copending U.S. patent application. Serial No. 699,478, filed November 29, 1957,1'in the name of Henn et a1. Following this color developing process, the colored photographs are rinsed in a tetramethylolcyclohexanol bath.
- a method of treating gelatino fully processed colored photographic transparencies comprising wetting the gelatino image carrying layer for 1-l0 minutes with an aqueous solution of 520% of a cyclic compound having the general formula:
- R is selected from the class consist ing of CO and COH, Y is methylol, and 2-3% by weight of a polymethylene glycol having 4-8 carbon atoms.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Unite States Patent TETRAMETHYLOLCYCLOHEXANOL TREAT- MENT TO PREVENT POPPING AND FAD- PING or TRANSPARENCIES AND FADING "or COLOR PRINTS Norman D. Clarke, Roy A. Jelfreys, and David G. Saunders, Harrow, England, assignors to Eastman Kodak Company, Rochester, NY, a corporation of New Jersey *No Drawing. Filed Jan. 26, 1959, Ser. No. 788,765
7 3 Claims. (CI. 96-55) This invention concerns the treatment of colored photographs, more particularly to a final rinse bath to stabilize the dyes present in the image layers.
Many of the colored photographic elements which are in use are subject to fading and the like due to light and heat during optical projection, and extreme humidity condition. Inasmuch as the colors alter unevenly, the color balance can be changed so that the color portrayal is no longer accurate. Often a deterioration of the colored image takes place resulting in the yellowing or browning of the colored photograph when stored in a heated atmosphere. In .some instances, staining or browning of the white areas occurs due to the deterioration of residual unused couplers left in the light sensitive areas after processing. This coupler deterioration arises due to the action of light and also due to the action of heat and high humidity. Another result of color instability is loss of the yellow or other color.
A problem peculiar to transparent photographic elements is that of avoiding popping of colored photographic transparencies during optical projection. Popping is a characteristic of most transparencies which occurs when the transparency is placed in the slide changer through which the light is transmitted. Due to the heat, the transparency buckles with a resulting change in focus which necessitates refocusing. Many solutions have been suggested for the problem, including lacquering the transparency, redesigning the projector to provide a cooled light, and the like. However, it has been desirable to find a simple treatment for the transparencies which will prevent them from popping without deleteriously effecting the transparency itself.
We have found a simple method of treating colour photographs after they have been processed which results in remarkable color stability even when subjected to ad verse conditions.
One object of this invention is to provide a method of stabilizing the colors in colored photographs. Another object is to provide stabilized colored transparencies which can be projected optically without popping. A further object is to provide a simple method of after-treatment for colored photographic elements which will stabilize the colors against deterioration or alteration.
The above objects are obtained by treatment of the photographic elements with an aqueous solution containing 520% by weight of a tetramethylol cyclic alcohol or ketone having 5-8 carbon atoms in the ring. The photographic element whether a print, a transparency or a negative is dipped in the bath of the cyclic alcohol or ketone for 1-10 minutes, although this period is not critical. Surplus liquid can be removed with a squeegee, rapid water wash or other means. The photographic element may then be dried at room temperature or more rapidly in an oven.
Patented May 9, 1961 n=13 R=CO or CHOH W, X, Y, Z=methylol groups A polymethylene glycol having from 4 to 8 carbon 5 atoms such as 2-methylpentane-2,4-diol may be added as a plasticizer in the treatment bath at a concentration of about 2-3% by weight. Other polymet'hylene glycols which may be used include hexyleneglycol, hexamethy1ene-l,6-diol, 3-methylpentane-1,5-diol, tetrarnethylene-l,4-diol, Z-ethoxyethanol and the like.
The following examples illustrate our invention but are not intended to limit it in any way.
Example 1 Fully processed colored transparencies of the type described in 11.8. Patent 2,304,939, containing three layers of light-sensitive emulsion, each layer being sensitive to a particular color, such as the blue-sensitive silver halide layer, green-sensitive silver halide layer, and red-sensitive silver halide layer were dipped in a solution of 8% tetramethylol cyclohexanol and 2% 2-methylpentaue2,4-diol for 2 minutes, squeegeed and dried at room temperature. These transparencies did not pop in a Kodaslide projector with a 250-watt lamp during 3 minutes. An untreated slide popped within 15 seconds.
Slides were also treated with 5, 10, 15 and 20% solutions of tetramethylolcyclohexanol, and with mixtures of 5%+2%, 10%+2%, 15%+2% and 10%+2.5% con centrations of tetramethylolcyclohexanol and 2-rnethylpentane-2,4-diol. None of the slides treated popped during 1 /2 minutes.
Example 2 Color transparencies of the type described in Example 1 were fully processed and washed. These transparencies were immersed in an aqueous solution of tetramethylolcyclohexanol for 10 minutes, squeegeed and dried. Together with a water-washed slide they were exposed to light from a SOD-watt tungsten filament lamp at a distance of 8.5 inches for hours in a Fadorneter, and at the same time cooled by a current of air blown through the Fadometer. The following table gives the approximate percentage loss of density (from an original density of 1.0) for the yellow and magenta images. The cyan dye Example Color prints prepared according to US. Patent 2,272,191, were processed, washed, and immersed for 10 minutes in an aqueous solution of tetramethylolcyclohexanol. The prints were squeegeed and dried. To-
Percent Density Loss In creased From 1.0 Stain (Blue reflection Prnit Treatment Density) Cyan Magenta Yellow Control 7 33 g 45 0.11 to 0.25 Water wash 7 46 50 0. 11 to O. 25 10% tetramethylol clohexanol 2 14 0. 12 to 0. 10
Example 4 Color transparencies of the type described in Example 1 are immersed in a 7.5% solution of 2:2:52S-tetramethylolcyclopentanone in water for 10 minutes, then removed from the solution, surplus liquid squeegeed oil, and dried.
Example 5 Color transparencies of the type described in Example 1 are immersed in a 7.5% solution of 2:2:6z6-tetramethylolcyclohexanone in water for minutes, then removed from the solution, surplus liquid squeegeed off, and dried.
Example 6 Color prints of the type of Example 3 are immersed in a 10% solution of 2:2:5:S-tetramethylolcyclopentanone in water for 10 minutes, then removed from the solution, surplus squeegeed oh, and dried.
Example 7 Color prints of the type of Example 3 are immersed in a 10% solution of 2:2:6:6rtetramethylolcyclohexanone in water for 10 minutes, then removed from the solution, surplus liquid squeegeed off, and dried.
Example 8 Color transparencies of the type described in Example 1 are immersed in an 8% solution of 2:2:6z6-tetramethylolcyclohexanol and 2% of 2-ethoxyethanol in water for 10 minutes, then removed from the solution, surplus liquid squeegeed off, and dried.
Example 9 Color transparencies of the type described in Example l are immersed in an 8% solution of 2:216:6-tetramethylolcyclohexanol and 2% tetramethylene-1z4-diol in water for 10 minutes, then removed from. the solution, surplus liquid squeegeed off, and dried.
Example 10 Color transparencies of the type described in Example 1 are immersed in a 10% solution of a mixture of 3- methyland 4-methyl-2: 2: 6 6-tetramethylolcyclohexanol in water for 10 minutes, then removed from the solution, surplus liquid squeegeed 011?, and dried.
Example 11 Color transparencies of the type described in Example 1 are immersed in an aqueous solution of 8% 2:2:6z6-
4 tetramethylolcyclohexanone and 2% hexyleneglycol in water for 10 minutes, then removed from the solution, surplus'liquid squeegeed OE, and dried.
Photographic colored elements which are operative in our invention include those-illustrated in the examples as well as those disclosed in U.S. Patent 2,296,306. They also include color positive print material coated on paper in which the color formers are present in the emulsion or are obtained using a selective second exposure'followed by development by developing solutions containing color formers and color developing agents. Other color elements include color reversible film, color negative film, and color reversible white printing mate: rial coated on an opaque base. M v 4 An example .of. a developing. process for colored photographic elements known as the E2 Process is disclosed in copending U.S. patent application. Serial No. 699,478, filed November 29, 1957,1'in the name of Henn et a1. Following this color developing process, the colored photographs are rinsed in a tetramethylolcyclohexanol bath.
We claim:
1. In a process of producing gelatino colored photographic images in a multicolor photographic element by exposing a silver halide photographic emulsion, color developing, bleaching, fixing and washing the photographic element, the improvement which comprises sta bilizing the dyes and preventing the discoloration of the photographic image and preventing popping, comprising rinsing the processed photographic image with an aqueous solution containing 520% of tetramethylolcyclohexanol for l-l0 minutes. 7 g
2. A method of treating gelatino fully processed colored photographic transparencies comprising wetting the gelatino image carrying layer for 1-l0 minutes with an aqueous solution of 520% of a cyclic compound having the general formula:
H don. Y' in which n is 0-2, R is selected from the class consist ing of CO and COH, Y is methylol, and 2-3% by weight of a polymethylene glycol having 4-8 carbon atoms.
References Cited in the file of this patent UNITED STATES PATENTS 2,725,305 Allen et al. Nov. 29, 1955 2,870,013 Jefireys Jan. 20, 1959 2,895,827
Callear et a1 July 21, 1959
Claims (1)
- 2. A METHOD OF TREATING GELATINO FULLY PROCESSED COLORED PHOTOGRAPHIC TRANSPARENCIES COMPRISING WETTING THE GELATINO IMAGE CARRYING LAYER FOR 1-10 MINUTES WITH AN AQUEOUS SOLUTION OF 5-20% OF A CYCLIC COMPOUND HAVING THE GENERAL FORMULA:
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US788765A US2983607A (en) | 1959-01-26 | 1959-01-26 | Tetramethylolcyclohexanol treatment to trevent popping and fading of transparencies and fading of color prints |
| GB2415/60A GB926284A (en) | 1959-01-26 | 1960-01-22 | Method of improving photographic transparencies and prints |
| FR816578A FR1246008A (en) | 1959-01-26 | 1960-01-25 | Photographic processing method and processing bath useful for the implementation of this method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US788765A US2983607A (en) | 1959-01-26 | 1959-01-26 | Tetramethylolcyclohexanol treatment to trevent popping and fading of transparencies and fading of color prints |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2983607A true US2983607A (en) | 1961-05-09 |
Family
ID=25145481
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US788765A Expired - Lifetime US2983607A (en) | 1959-01-26 | 1959-01-26 | Tetramethylolcyclohexanol treatment to trevent popping and fading of transparencies and fading of color prints |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US2983607A (en) |
| FR (1) | FR1246008A (en) |
| GB (1) | GB926284A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4786583A (en) * | 1987-06-22 | 1988-11-22 | Eastman Kodak Company | Stabilizing bath for use in photographic processing |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2725305A (en) * | 1952-01-02 | 1955-11-29 | Eastman Kodak Co | Hardening gelatin emulsions and gelatin solutions |
| US2870013A (en) * | 1956-11-29 | 1959-01-20 | Eastman Kodak Co | Hardening of gelatin with 2,3 dihydroxy dioxane |
| US2895827A (en) * | 1956-10-24 | 1959-07-21 | Eastman Kodak Co | Photographic paper base |
-
1959
- 1959-01-26 US US788765A patent/US2983607A/en not_active Expired - Lifetime
-
1960
- 1960-01-22 GB GB2415/60A patent/GB926284A/en not_active Expired
- 1960-01-25 FR FR816578A patent/FR1246008A/en not_active Expired
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2725305A (en) * | 1952-01-02 | 1955-11-29 | Eastman Kodak Co | Hardening gelatin emulsions and gelatin solutions |
| US2895827A (en) * | 1956-10-24 | 1959-07-21 | Eastman Kodak Co | Photographic paper base |
| US2870013A (en) * | 1956-11-29 | 1959-01-20 | Eastman Kodak Co | Hardening of gelatin with 2,3 dihydroxy dioxane |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4786583A (en) * | 1987-06-22 | 1988-11-22 | Eastman Kodak Company | Stabilizing bath for use in photographic processing |
Also Published As
| Publication number | Publication date |
|---|---|
| GB926284A (en) | 1963-05-15 |
| FR1246008A (en) | 1960-11-10 |
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