US2458376A - Photographic developer antioxidants - Google Patents

Photographic developer antioxidants Download PDF

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Publication number
US2458376A
US2458376A US654527A US65452746A US2458376A US 2458376 A US2458376 A US 2458376A US 654527 A US654527 A US 654527A US 65452746 A US65452746 A US 65452746A US 2458376 A US2458376 A US 2458376A
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US
United States
Prior art keywords
bisulfite
sulfite
developer
antioxidants
cyclohexanone
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
Application number
US654527A
Inventor
Richard W Henn
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eastman Kodak Co
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Eastman Kodak Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co
Priority to US654527A priority Critical patent/US2458376A/en
Priority to FR944359D priority patent/FR944359A/en
Priority to GB7198/47A priority patent/GB626998A/en
Application granted granted Critical
Publication of US2458376A publication Critical patent/US2458376A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C5/00Photographic processes or agents therefor; Regeneration of such processing agents
    • G03C5/26Processes using silver-salt-containing photosensitive materials or agents therefor
    • G03C5/29Development processes or agents therefor
    • G03C5/305Additives other than developers

Definitions

  • the bisulfite addition compounds are believed to undergo partial hydrolysis in the developing solutions, yielding a supply of sulfite ions which, when destroyed by oxidation, is replaced as the result of further hydrolysis of the original complex in accordance with the normal equilibrium reactions.
  • This reaction may be represented as follows:
  • These developing agents can not develop at all when used by themselves. In order to be effective they must be employed in alkaline solution, and their energy depends upon the amount of alkali present. Since developers are reducing agents and have a great affinity for oxygen, developing solutions containin onl the developing agent and the alkali would be rapidly spoiled from oxidation by the air. In order to preserve the developer, there is added to the developing solution, in addition to the reducing agent and alkali, some sodium sulfite or sodium bisulfite, which protects the developer from the oxygen of the air.
  • a developing solution designed for maximum contrast with process materials must produce density readily in the photographic negative.
  • a high alkali concentration is necessary for such rapid development. But, the more strongly alkaline the developer, the more rapid the rate of oxidation, and therefore an increased amount of sodium bisulfite preservative is required.
  • an object of the gresent invention to provide a photographic developing solution having a high alkalinity, low sulfite ion concentration, and high resistance to oxidation.
  • a further object is to provide an improved developer antioxidant of the carbonyl-bisulfite addition product type.
  • the carbonyl-bisulfite addition compounds may be used in crystalline form or as mixtures of the carbonyl compound and an alkali metal sulfite or other sulfite. When using the mixture it is desirable to employ an excess of the carbonyl compound to shift the equilibrium to the left and further decrease the sulfite ion concentration. Since the concentration of the sulfite ion is controlling, sulfites other than sodium bisulfite may be used in forming the addition compounds, for example, sodium sulfite, potassium sulfite, and other alkali metal sulfites. Metabisulfites, bi-
  • sulfites and other soluble sulfites may also be employed.
  • Example II The following developer was found to give as much contrast as a developer containing only 1 gram of sodium sulfite per liter,
  • a composition of matter adapted to form a developing solution having a low sulfite ion concentration and a high resistance to oxidation when dissolved in water in the presence of a strong inorganic base comprising a photographic silver halide developing agent and a member selected from the class consisting of cyclohexanone-bisulfite, methyl cyclohexanone-bisulfites,
  • a composition of matter adapted to form a developing solution having a low sulfite ion concentration and a high resistance to oxidation when dissolved in water in the presence of a strong inorganic base comprising a photographic silver halide developing agent and a compound of cyclohexanone with sodium bisulfite.
  • a composition of matter adapted to form a developing solution having a low sulfite ion concentration and a high resistance to oxidation 5.
  • a photographic developer comprising hydroquinone, sodium hydroxide and oyclohexanoneg sodium bisulfite.
  • a photographic developer comprising hydroquinone, sodium hydroxida'and p-metliyl cyclohexanone-sodium bisulfite.

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  • 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

Patented Jan. 4, 1949 UNlTED STATES PATENT OFFICE PHOTOGRAPHIC DEVELOPER AN TIOXIDAN T S Richard W. Henn, Rochester, N. Y., assignor to Eastman Kodak Company, Rochester, N. Y., a corporation of New Jersey No Drawing. Application March 14, 1946, Serial No. 654,527
7 Claims.
The bisulfite addition compounds are believed to undergo partial hydrolysis in the developing solutions, yielding a supply of sulfite ions which, when destroyed by oxidation, is replaced as the result of further hydrolysis of the original complex in accordance with the normal equilibrium reactions. This reaction may be represented as follows:
Carbonyl-NaHSOi Carbonyl compound+Na++H++SOr fate and glycin. These developing agents can not develop at all when used by themselves. In order to be effective they must be employed in alkaline solution, and their energy depends upon the amount of alkali present. Since developers are reducing agents and have a great affinity for oxygen, developing solutions containin onl the developing agent and the alkali would be rapidly spoiled from oxidation by the air. In order to preserve the developer, there is added to the developing solution, in addition to the reducing agent and alkali, some sodium sulfite or sodium bisulfite, which protects the developer from the oxygen of the air.
A developing solution designed for maximum contrast with process materials must produce density readily in the photographic negative. A high alkali concentration is necessary for such rapid development. But, the more strongly alkaline the developer, the more rapid the rate of oxidation, and therefore an increased amount of sodium bisulfite preservative is required. There are occasions when it is desirable to maintain an extremely high concentration of alkali in the developer with pH over 12, and yet at the same time keep the sulfite ion concentration low to allow high contrast development. This is the case, for example, when using tanning developers, and high contrast process developers. To accomplish this it has already been proposed to add to developers carbonyl-bisulfite addition products of the acetone-bisulfite and formaldehyde-bisulfite types.
It is, therefore, an object of the gresent invention to provide a photographic developing solution having a high alkalinity, low sulfite ion concentration, and high resistance to oxidation. A further object is to provide an improved developer antioxidant of the carbonyl-bisulfite addition product type.
I have found that highly improved oxidation resisting developing solutions may be obtained by the addition to such solutions of cyclohexanonebisulfite and substituted cyclohexanone-bisulfite addition products.
The carbonyl-bisulfite addition compounds may be used in crystalline form or as mixtures of the carbonyl compound and an alkali metal sulfite or other sulfite. When using the mixture it is desirable to employ an excess of the carbonyl compound to shift the equilibrium to the left and further decrease the sulfite ion concentration. Since the concentration of the sulfite ion is controlling, sulfites other than sodium bisulfite may be used in forming the addition compounds, for example, sodium sulfite, potassium sulfite, and other alkali metal sulfites. Metabisulfites, bi-
sulfites, and other soluble sulfites may also be employed.
In determining the effectiveness of my new developer antioxidants I have compared them with other carbonyl-bisulfite addition products added to highly alkaline hydroquinone developing solutions. The developing solution in each case was exposed to air and the time taken'to darken to a given level determined with the aid of a colorimeter. The concenrations of the carbonylbisulfite addition compounds added were found equivalent in allowing similar high contrast development.
Example I.Oa:z'dation test-To a developer containing 5 grams of hydroquinone, 25 grams of sodium hydroxide and 1000 cc. of water, the following concentrations of carbonyl-bisulfite addition compounds were added:
Example II.The following developer was found to give as much contrast as a developer containing only 1 gram of sodium sulfite per liter,
yet to oxidize as slowly as one containing 5 grams of sulfite per liter:
Hydroquinone grams 5.0 Sodium hydroxide do 25.0 Methyl benzotriazole do 0.2' Cyclohexanonesodium bisulfite do 20.0 Water to cc 1000 The developers prepared according to myinvention give exceptionally high contrast. Gamma values of from 6 to 10 have been achieved,
the H. and D. curve having a very short toe.v
High contrast of this order can be obtained only when the sulfite ion concentration is kept to a minimum as in the case of developers containing the cyclohexanone-bisulfite antioxidants.
I claim:
1. A composition of matter adapted to form a developing solution having a low sulfite ion concentration and a high resistance to oxidation when dissolved in water in the presence of a strong inorganic base, comprising a photographic silver halide developing agent and a member selected from the class consisting of cyclohexanone-bisulfite, methyl cyclohexanone-bisulfites,
mixtures of cyclohexanone and a soluble sulfite,
and mixtures of cyclohexanone and asoluble bisulfite.
2. A composition of matter adapted to form a developing solution having a low sulfite ion concentration and a high resistance to oxidation when dissolved in water in the presence of a strong inorganic base, comprising a photographic silver halide developing agent and a compound of cyclohexanone with sodium bisulfite.
3. A composition of matter adapted to form a developing solution having a low sulfite ion concentration and a high resistance to oxidation 5. A photographic developer comprising hydroquinone, sodium hydroxide and oyclohexanoneg sodium bisulfite. 6, A composition of matter adapted to form a developing solution having a low sulfite ion concentration and a high resistance to oxidation when dissolved in water in the presence of a base comprising a silver halide developing agent, cyclohexanone, and a soluble sulfite.
7. A photographic developer comprising hydroquinone, sodium hydroxida'and p-metliyl cyclohexanone-sodium bisulfite.
RICHARD W.
REFERENCES CITED The following references are of record inthe file of this patent:
UNITED STATES PATENTS Number Name Date 2,313,523 Donovan et a1. Mar. 9, 1943 OTHER REFERENCES Lumiere et al.,,Ueber die Verwendung der Aldehyde und der Acetone usw. Eders J ahrbuch tor Photographic, 1897, 11 pages, 30 to 36, inclusive. (Copyin ,S. L.)
US654527A 1946-03-14 1946-03-14 Photographic developer antioxidants Expired - Lifetime US2458376A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US654527A US2458376A (en) 1946-03-14 1946-03-14 Photographic developer antioxidants
FR944359D FR944359A (en) 1946-03-14 1947-02-26 Antioxidant enhancements for photographic developers
GB7198/47A GB626998A (en) 1946-03-14 1947-03-14 Improvements in photographic developers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US654527A US2458376A (en) 1946-03-14 1946-03-14 Photographic developer antioxidants

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US2458376A true US2458376A (en) 1949-01-04

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Country Link
US (1) US2458376A (en)
FR (1) FR944359A (en)
GB (1) GB626998A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2675318A (en) * 1951-06-27 1954-04-13 Eastman Kodak Co Hydroquinone monosulfonate in direct positive photographic developers
US2843483A (en) * 1955-10-03 1958-07-15 Eastman Kodak Co Photographic developer
US3079858A (en) * 1956-02-25 1963-03-05 Agfa Ag Process for the production of printing forms

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2313523A (en) * 1940-06-18 1943-03-09 Eastman Kodak Co Photographic material

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2313523A (en) * 1940-06-18 1943-03-09 Eastman Kodak Co Photographic material

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2675318A (en) * 1951-06-27 1954-04-13 Eastman Kodak Co Hydroquinone monosulfonate in direct positive photographic developers
US2843483A (en) * 1955-10-03 1958-07-15 Eastman Kodak Co Photographic developer
US3079858A (en) * 1956-02-25 1963-03-05 Agfa Ag Process for the production of printing forms

Also Published As

Publication number Publication date
FR944359A (en) 1949-04-04
GB626998A (en) 1949-07-25

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