US2415666A - Ascorbic acid in photographic developing solutions - Google Patents
Ascorbic acid in photographic developing solutions Download PDFInfo
- Publication number
- US2415666A US2415666A US494246A US49424643A US2415666A US 2415666 A US2415666 A US 2415666A US 494246 A US494246 A US 494246A US 49424643 A US49424643 A US 49424643A US 2415666 A US2415666 A US 2415666A
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- United States
- Prior art keywords
- ascorbic acid
- developing
- tanning
- solution
- photographic
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- 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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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/29—Development processes or agents therefor
- G03C5/305—Additives other than developers
Definitions
- This invention relates to anti-oxidants in photographic developing solutions.
- tanning developers In the production of relief images in gelatin, one of the most rapid methods involves the use of so-called tanning developers. These develop-- ers are usually of the catechol-sodium hydroxide, or pyrogallol-sodium hydroxide type, which depend, for their operation, upon the fact that the reaction product of the development hardens the gelatin in the immediate vicinity of the silver halide being reduced. Because of the instability of these developing agents at the pH at which they are used, they oxidize quite rapidly, being useful only for a relatively short time. It has been the practice in the past to use these solutions a very short time, usually only for one development, then to discard the solution. Since the formulas of this type must be kept as two stock solutions, a great deal of time is lost mixing and cooling a fresh bath for each sample.
- Sodium sulfite which is the anti-oxidant cmmonly used in developing solutions, cannot be used in tanning developers since a quantity sufficient to prevent oxidation for any length of time would greatly reduce or completely destroy the hardening action of the developer (Neblette Photography Principles and Practice, 4th edition, 1942, page 766).
- Tanning developers may tolerate a small amount of sulfite but, when an amount greater than about 2 grams per liter is used, the tanning action is so slight as to render the solution impracticableas a tanning developer.
- an object of the present invention to provide a tanning photographic developer which is stable to aerial oxidation.
- a further object is to provide a novel anti-oxidant for photographic developing solutions.
- both the laevo ascorbic acid and the dextro-iso-ascorbic acid possess the property of reducing aerial oxidation of photographic developing solutions.
- laevo ascorbic acid a concentration of 4 grams per liter of developing solution was found to be satisfactory. Concentrations as low as 0.1 gram per liter were tested and showed some action and amounts as great as grams or more per liter were also found to be satisfactory.
- the ascorbic acids may also be used as their alkali metal salts, for example, as the sodium salts.
- Ascorbic acid is believed to have the following Iso ascorbic acid is an isomeric form of ascorbic acid and is believed to have the same structural formula.
- ascorbic acid In addition to its action in tanning developers, ascorbic acid also decreases the aerial oxidation of non-tanning developers. Developing solutions containing considerable sodium sulfite may be improved and their keeping time increased by the addition of ascorbic acid or isoascorbic acid to the developing solution. In such developing solutions containing sulfite, the addition to the solution of a small amount of ascorbic acid will provide better keeping properties than the addition of the same quantity of sodium sulfite.
- Ascorbic acid and isoascorbic acid may also be used to prevent the aerial oxidation of Elon-hydroquinone developers such as the Kodak D-72 developer but they are not so effective in these developers as in developers containing dihydroxy benzenes such as pyrogallol. pyrocatechol, or hydroquinone, as the developing agent.
- A is mixed with B and 50 cc. of formaldehyde are added.
- This developing solution was found to discolor and darken on mixing and standing for about one hour.
- 10 grains of the sodium salt of isoascorbic acid were added to one liter of the developing solution, the time required for the solution to darken was increased to more than 20 hours.
- ascorbic acid and its isomers are powerful anti-oxidants in solutions of dihydroxy benzene developing agents such as catechol, and that they are active even in the presence of considerable sulfite. They do not destroy the tanning action of tanning developers containing little or no sulfite and in such developers are very effective in improving the keeping properties of the developing solution. They may be used inaminophenol developing solutions but appear to be less efi'ective in such solutions than in solutions of phenolic developers such as catechol.
- a tanning photographic developer free of sulfite containing an alkaline solution of a dihydroxy benzene developing agent and from about 0.1 gram to at least 10 grams per liter of ascorbic acid.
- a photographic developing solution possessin stability to aerial oxidation comprising an alkaline solution of an ortho-dihydroxy benzene photographic developing agent and an aerialoxidation-inhibiting amount of ascorbic acid.
- a photographic developing solution possessing stability to aerial oxidation comprising an aqueous sodium hydroxide solution of an orthodihydroxy benzene photographic developing agent and an aerial-oxidation-inhibiting amount of ascorbic acid.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Description
Patented Feb. 11, 1947 ASCORBIC ACID IN PHOTOGRAPH-HG DEVELOPING SOLUTIQNS Arnold Weissberger and Hugo A. Kurtzner, Rochester, N. Y., assignors to Eastman Kodak Company, Rochester, N. Y., a corporation of New Jersey No Drawing. Application July 10, 1943, Serial No. 494,246
'7 Claims.
This invention relates to anti-oxidants in photographic developing solutions.
In the production of relief images in gelatin, one of the most rapid methods involves the use of so-called tanning developers. These develop-- ers are usually of the catechol-sodium hydroxide, or pyrogallol-sodium hydroxide type, which depend, for their operation, upon the fact that the reaction product of the development hardens the gelatin in the immediate vicinity of the silver halide being reduced. Because of the instability of these developing agents at the pH at which they are used, they oxidize quite rapidly, being useful only for a relatively short time. It has been the practice in the past to use these solutions a very short time, usually only for one development, then to discard the solution. Since the formulas of this type must be kept as two stock solutions, a great deal of time is lost mixing and cooling a fresh bath for each sample.
Sodium sulfite, which is the anti-oxidant cmmonly used in developing solutions, cannot be used in tanning developers since a quantity sufficient to prevent oxidation for any length of time would greatly reduce or completely destroy the hardening action of the developer (Neblette Photography Principles and Practice, 4th edition, 1942, page 766). Tanning developers may tolerate a small amount of sulfite but, when an amount greater than about 2 grams per liter is used, the tanning action is so slight as to render the solution impracticableas a tanning developer.
It is, therefore, an object of the present invention to provide a tanning photographic developer which is stable to aerial oxidation. A further object is to provide a novel anti-oxidant for photographic developing solutions.
These objects are accomplished by incorporating in a silver halide developing solution, especially a solution of a tanning developer, one or more of the forms of ascorbic acid.
We have found that both the laevo ascorbic acid and the dextro-iso-ascorbic acid possess the property of reducing aerial oxidation of photographic developing solutions. With laevo ascorbic acid a concentration of 4 grams per liter of developing solution was found to be satisfactory. Concentrations as low as 0.1 gram per liter were tested and showed some action and amounts as great as grams or more per liter were also found to be satisfactory. The ascorbic acids may also be used as their alkali metal salts, for example, as the sodium salts.
Ascorbic acid is believed to have the following Iso ascorbic acid is an isomeric form of ascorbic acid and is believed to have the same structural formula.
In addition to its action in tanning developers, ascorbic acid also decreases the aerial oxidation of non-tanning developers. Developing solutions containing considerable sodium sulfite may be improved and their keeping time increased by the addition of ascorbic acid or isoascorbic acid to the developing solution. In such developing solutions containing sulfite, the addition to the solution of a small amount of ascorbic acid will provide better keeping properties than the addition of the same quantity of sodium sulfite.
Ascorbic acid and isoascorbic acid may also be used to prevent the aerial oxidation of Elon-hydroquinone developers such as the Kodak D-72 developer but they are not so effective in these developers as in developers containing dihydroxy benzenes such as pyrogallol. pyrocatechol, or hydroquinone, as the developing agent.
Our invention will be further illustrated by reference to the following specific examples:
EXAMPLE 1 A tanning photographic developer of the following composition was found to have greatly improved keeping properties over the same solution containing no ascorbic acid:
Sodium sulfate grams 150 Pyrocatechol do 8 Potassium bromide do 1 Laevo ascorbic acid do 4 Water to cubic centimeters" 900 Sodium hydroxide (10% solution) cubic centimeters" EXAMPLE 2 The sodium salt of isoascorbic acid was added in various amounts to the following high-energy Elon-catechol developer which had a pH of 9.5.
Combine A and B immediately before using. When this developer was mixed and allowed to stand, it showed darkening in about 10 minutes' The addition of increasing amounts of sodium salt of isoascorbic acid to portions of the solution improved the keeping of the developer as follows:
Time for developer Grams per liter to darken min. min. min. 40 min.
Over 1 hour. 2 hours.
EXAMPLE 3 The sodium salt of isoascorbic acid was found to improve the keeping of the following non-tan.- ning developing solution:
For use, A is mixed with B and 50 cc. of formaldehyde are added.
This developing solution was found to discolor and darken on mixing and standing for about one hour. When 10 grains of the sodium salt of isoascorbic acid were added to one liter of the developing solution, the time required for the solution to darken was increased to more than 20 hours.
We have found, therefore, that ascorbic acid and its isomers are powerful anti-oxidants in solutions of dihydroxy benzene developing agents such as catechol, and that they are active even in the presence of considerable sulfite. They do not destroy the tanning action of tanning developers containing little or no sulfite and in such developers are very effective in improving the keeping properties of the developing solution. They may be used inaminophenol developing solutions but appear to be less efi'ective in such solutions than in solutions of phenolic developers such as catechol.
The examples and modifications included herein are illustrative only and it will be understood that our invention is to be taken as limited only by the scope of the appended claims.
We claim:
1. A tanning photographic developer substantially free of sulfite, containing an alkaline solution of a dihydroxy benzene developing agent and an aerial-oxidation-inhibiting amount of ascorbic acid.
2. A tanning photographic developer free of sulfite, containing an alkaline solution of a dihydroxy benzene developing agent and from about 0.1 gram to at least 10 grams per liter of ascorbic acid.
3. A tanning photographic developer free of sulfite, containing an alkaline solution of pyrocatechol as a developing agent and from about 0.1 gram to at least 10 grams per liter of ascorbic acid.
4. A tanning photographic developer free of suliite, containing an alkaline solution of pyrocatechol as a developing agent and about 4 grams per liter of ascorbic acid.
5. A tanning photographic developer free of sulfite, containing an alkaline solution of pyrocatechol as a developing agent and about 4 grams per liter of isoascorbic acid.
6. A photographic developing solution possessin stability to aerial oxidation, comprising an alkaline solution of an ortho-dihydroxy benzene photographic developing agent and an aerialoxidation-inhibiting amount of ascorbic acid.
'7. A photographic developing solution possessing stability to aerial oxidation, comprising an aqueous sodium hydroxide solution of an orthodihydroxy benzene photographic developing agent and an aerial-oxidation-inhibiting amount of ascorbic acid.
ARNOLD WEISSBERGER. HUGO A, KURTZNER.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Name Date Christensen Oct. 30, 1923 Number ess, MacMillan Co., New York, 1942 (pages 357,
381 and 383 cited). (Copy in Division '7.)
Henney and Dudley, Handbook of Photography, McGraw-Hill, New York, 1939 (pp. 333, 338 and 339 cited). (Copy in Division 7.)
Bills Science, V01. 81, p. 257-8, March 8, 1935. (Photostat copy in -88-AA, Division 7).
Cuisinier, Rev. Franc. Pilot, vol. 10, June 15, 1929, pp. -6. (Photostat copy in 95-88AA, Division '7.)
Cuisinier, Photographe, vol. 16, July 6, 1929, p. 288. (Photostat copy in 95-88AA, Division 7.) Golumbic et al., The Antioxygenic Action of Ascorbic Acid with Hydroquinone and related Compounds, Journal American Chemical Society, May, 1941, vol. 63, pp. 1279-80. (Photostatic copy in Div. 43 167-81 (box 9).)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US494246A US2415666A (en) | 1943-07-10 | 1943-07-10 | Ascorbic acid in photographic developing solutions |
| FR938575D FR938575A (en) | 1943-07-10 | 1946-08-26 | Antioxidants for developers and developers containing them |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US494246A US2415666A (en) | 1943-07-10 | 1943-07-10 | Ascorbic acid in photographic developing solutions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2415666A true US2415666A (en) | 1947-02-11 |
Family
ID=23963683
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US494246A Expired - Lifetime US2415666A (en) | 1943-07-10 | 1943-07-10 | Ascorbic acid in photographic developing solutions |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US2415666A (en) |
| FR (1) | FR938575A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2607686A (en) * | 1949-10-18 | 1952-08-19 | Gen Aniline & Film Corp | Process of obtaining cold sepia tones |
| US2626215A (en) * | 1950-03-03 | 1953-01-20 | Miracol R Ltd | Method of developing multilayer color films |
| US2635048A (en) * | 1948-07-06 | 1953-04-14 | Polaroid Corp | Photographic transfer product and process |
| US2644756A (en) * | 1947-02-08 | 1953-07-07 | Polaroid Corp | Photographic process for forming a positive transfer image |
| US2653872A (en) * | 1947-01-28 | 1953-09-29 | Polaroid Corp | Photographic product comprising a rupturable container carrying a liquid for processing said product |
| US3305363A (en) * | 1962-11-13 | 1967-02-21 | Eastman Kodak Co | Photographic development promoters |
| US3330661A (en) * | 1962-11-13 | 1967-07-11 | Eastman Kodak Co | Photographic development precursors |
| US3512981A (en) * | 1968-02-05 | 1970-05-19 | Pako Corp | Stable photographic developers containing ascorbic acid |
| US4324853A (en) * | 1979-07-18 | 1982-04-13 | Polaroid Corporation | Photographic processing composition containing polyol |
| US4699868A (en) * | 1984-03-02 | 1987-10-13 | Minnesota Mining And Manufacturing Company | Photographic tanning developer formulation |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1472048A (en) * | 1918-11-20 | 1923-10-30 | Christensen Jens Herman | Method of hardening of photographic films |
-
1943
- 1943-07-10 US US494246A patent/US2415666A/en not_active Expired - Lifetime
-
1946
- 1946-08-26 FR FR938575D patent/FR938575A/en not_active Expired
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1472048A (en) * | 1918-11-20 | 1923-10-30 | Christensen Jens Herman | Method of hardening of photographic films |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2653872A (en) * | 1947-01-28 | 1953-09-29 | Polaroid Corp | Photographic product comprising a rupturable container carrying a liquid for processing said product |
| US2644756A (en) * | 1947-02-08 | 1953-07-07 | Polaroid Corp | Photographic process for forming a positive transfer image |
| US2635048A (en) * | 1948-07-06 | 1953-04-14 | Polaroid Corp | Photographic transfer product and process |
| US2607686A (en) * | 1949-10-18 | 1952-08-19 | Gen Aniline & Film Corp | Process of obtaining cold sepia tones |
| US2626215A (en) * | 1950-03-03 | 1953-01-20 | Miracol R Ltd | Method of developing multilayer color films |
| US3305363A (en) * | 1962-11-13 | 1967-02-21 | Eastman Kodak Co | Photographic development promoters |
| US3330661A (en) * | 1962-11-13 | 1967-07-11 | Eastman Kodak Co | Photographic development precursors |
| US3512981A (en) * | 1968-02-05 | 1970-05-19 | Pako Corp | Stable photographic developers containing ascorbic acid |
| US4324853A (en) * | 1979-07-18 | 1982-04-13 | Polaroid Corporation | Photographic processing composition containing polyol |
| US4699868A (en) * | 1984-03-02 | 1987-10-13 | Minnesota Mining And Manufacturing Company | Photographic tanning developer formulation |
Also Published As
| Publication number | Publication date |
|---|---|
| FR938575A (en) | 1948-10-19 |
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