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Publication numberUS3623872 A
Publication typeGrant
Publication dateNov 30, 1971
Filing dateApr 16, 1970
Priority dateApr 29, 1969
Also published asDE1921740A1
Publication numberUS 3623872 A, US 3623872A, US-A-3623872, US3623872 A, US3623872A
InventorsWerner Berthold, Anita Von Konig
Original AssigneeAgfa Gevaert Ag
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Stabilisation of developed photographic images
US 3623872 A
Abstract  available in
Previous page
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Claims  available in
Description  (OCR text may contain errors)

United States Patent *Olfice 3,623,872 Patented Nov. 30, 1971 US. C]. 96-61 4 Claims ABSTRACT OF THE DISCLOSURE Exposed and developed photographic silver images can be stabilised by treating the layer containing the exposed image with a compound which reacts with the silver halide in the unexposed and undeveloped areas of the layer to form a light-insensitive reaction product. Fading of the silver images thus produced is prevented by performing the development in the presence of heterocyclic carboxylalkyl mercapto compounds.

Stabilisation of developed photographic images The invention relates to a process for the production of photographic images by exposure, development and subsequent stabilisation, development being carried out in the presence of heterocyclic carboxyalkyl mercapto compounds which improve the stability of the silver image even after prolonged storage under extreme climatic conditions.

It is known to stabilise developed photographic images with complex forming compounds in rapid photographic reproduction processes as a substitute for conventional fixing with sodium thiosulfate followed by washing. In contrast to the method of fixing with sodium thiosulfate, in these stabilizing processes the silver salts remain in the unexposed and undeveloped parts of the layer in the form of a light-insensitive reaction product of the stabilising compound with the original silver halides. Stabilization of developed photographic materials has, however, certain disadvantages. One disadvantage is that nearly all substances which form complexes with silver halides attack metallic silver and hence the photographic image, converting the silver into a complex compound or simple silver salt. This leads to fading of the silver image or to a change in the color of the image silver from black to a. brownish tone. This undesired elfect occurs particularly in a moist atmosphere.

Fading of the black image area can be prevented by adding to the stabilising bath heterocyclic mercapto compounds such as 1-phenyl-S-mercaptotetrazole. However, the usual compounds of this type are only sparingly soluble in the acid stabiliser solutions so that it is difiicult to apply a sufiicient quantity of these compounds. They cannot be added in the required quantity to the emulsions because of their development inhibiting effect.

Fading of the black image areas can also be prevented by adding to the emulsion compounds which only decompose in alkaline solution to yield a mercapto compound. Such compounds, however, cannot be added to the emulsion in sufiicient quantities to improve satisfactorily the keeping quality of the stabilised image on prolonged storage under extreme climatic conditions.

It is among the objects of the present invention to provide compounds which do not show the disadvantages referred to above, and which are stabilising black silver images particularly upon prolonged storage under extreme climatic conditions.

We now have found a process for the production of photographic images including the steps of exposing a supported silver halide emulsion layer, developing and stabilising the exposed and developed layer wherein development is carried out with a bath which contains at least one heterocyclic compound of the following formulae:

wherein n is 1 to 3.

Suitable compounds are summarized in the following table:

The preparation of these compounds is described in US. Patent No. 3,330,663.

For operating the process according to the invention, conventional light-sensitive photographic materials having at least one silver halide emulsion layer are suitable. The light-sensitive emulsions may contain any silver halides, such as silver chloride or silver bromide, if desired with a small proportion of silver iodide. Emulsions which have a high silver chloride content are preferred.

The binders for the light-sensitive layers may be the usual water-permeable layer-forming substances, particularly proteins, preferably gelatine.

Furthermore, the emulsions may contain alkylene oxide polymerisation products as chemical sensitizers. They may also contain the known stabilizers.

In addition, the emulsions may contain developers or developer combinations of the type hydroquinone, pyrocatechol, aminophenol, compounds of the pyrazolidone series, phenylene diamine derivatives and the like, antioxidants for the developer, e.g. potassium metalbisulfite, aldehyde and ketone bisulfite, matting agents and brightening agents.

Development is carried out in the usual manner, using known developers. According to a preferred method of carrying out the invention, the developer is added to the photographic material and development is initiated by treatment with an alkaline aqueous bath, hereinafter referred to as an activator bath.

The concentration of the compounds for use according to the invention in the development bath may vary within wide limits. The concentration depends upon the photographic material used and the nature of the developer. The optimum concentrations for a particular reproduction process can be determined by a few simple laboratory tests. Amounts of 0.5 to 10 g. per liter of treatment bath, preferably 1 to 5 g. per liter, have generally been found to be sufficient.

Suitable stabilising agents, i.e. compounds which are capable of converting the silver halide remaining after development into a compound which is not sensitive to light, have been described e.g. in British Patents Nos. 631,184 or 959,807 and in U.S. Patent No. 2,525,532 or French Patent No. 1,237,454. Ammonium thiocyanate, and alkali metal thiocyanates, e.g. sodium or potassium thiocyanate, have been found to be particularly suitable.

These stabilising baths may also contain the usual other additives such as alkali metal sulfites or metabisulfites or cycloalkanone bisulfites, acetic acid or its salts and organic compounds, particularly additional heterocyclic compounds which contain mercapto groups, such as l-phenyl- S-mercaptotetrazole, which form sparingly soluble silver salts.

3 EXAMPLE 1 A light-sensitive photographic material comprising a supported silver chloride gelatin emulsion layer which emulsion layer contains 0.2 mol of silver halide with a silver iodide content of less than 0.1 mol percent of silver iodide per kg. of emulsion (amount of silver in the form of silver halide 1.3 g./m. and hydroquinone (12 g. of hydroquinone per kg. of emulsion) is exposed to form an image and developed in the following activator solution:

50 g. of sodium hydroxide 40 g. of anhydrous sodium sulfite 2 g. of potassium bromide 1 g. of 1-phenylpyrazolidone-(3) made up to 1 liter with water.

The compounds shown in the following table are added to the above activator solution. The quantities added are shown in the table.

The developed material is then treated with the following stabilising solution:

250 g. of ammonium thiocyanate 145 g. of potassium metabisulfite 100 ml. of a 3% aqueous solution of formaldehyde 25 ml. of 60% acetic acid,

made up to 1 liter with water.

The samples are processed in a two-bath development apparatus customarily employed. The treatment time is about 1 t 5 seconds in the activator bath and about 2 to seconds in the stabilising bath.

To test the stability in storage of the silver image, a portion of the copy is kept over water in a vessel for 24 hours.

Several of these uniformly moist portions of the copy are inserted into a polyethylene container and this container is placed in a bag containing 30 ml. of water and sealed. The sealed containers are stored in a heating cupboard at 60 C. for 5, 24 and 48 hours, respectively, and the change of the silver image which has taken place after this time is examined.

Whereas the silver image of the copies produced according to the invention remains black or dark brown to black depending on the time of storage, under the above condition the comparison sample shows discoloration varying from brown to pale brown. The maximum density of .4 the various fresh, air-dried materials and those which have been stored in moist heat is measured in a densitometer. The following results are obtained:

TABLE Maximum density after storage Concenin moist heat for- Compound added tration, Air N o. g./l. dried 5 hours 24 hours 48 hours We claim:

1. A process for the production of photographic images by exposure of a photographic material which has at least one silver halide emulsion layer, development and stabilisation of the unexposed and undeveloped silver halide, wherein development is performed with a bath containing at least one compound of the following formula or salts thereof:

References Cited UNITED STATES PATENTS 3,330,663 7/1967 Weyde 96-114.3

NORMAN G. TORCHIN, Primary Examiner M. F. KELLEY, Assistant Examiner US. Cl. X.R. 96-66, 95

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3981731 *Nov 4, 1975Sep 21, 1976Agfa-Gevaert, A.G.Stabilization of developed photographic images
US4371610 *Jul 24, 1981Feb 1, 1983Fuji Photo Film Co., Ltd.Process for development-processing silver halide light-sensitive material
US4675274 *Jul 19, 1985Jun 23, 1987Fuji Photo Film Co., Ltd.Method for developing color reversal photographic materials
DE3525900A1 *Jul 19, 1985Jan 23, 1986Fuji Photo Film Co LtdVerfahren zur entwicklung von photographischen farbumkehrmaterialien
DE3525900B4 *Jul 19, 1985Dec 29, 2005Fuji Photo Film Co., Ltd., Minami-AshigaraVerfahren zur Verarbeitung eines bildweise belichteten photographischen Farbumkehrsilberhalogenidmaterials
U.S. Classification430/405, 430/429, 430/963
International ClassificationG03C5/305, G03C5/39, G03C1/43
Cooperative ClassificationG03C5/305, G03C5/39, Y10S430/164, G03C1/43
European ClassificationG03C5/305, G03C5/39, G03C1/43