This invention relates to photographic bleach compositions and to methods of photographic processing employing such compositions.

Bleach baths are widely used in photographic colour processing to remove image silver so that only dye image remains. In many instances it is convenient to use a combined bleach and fix bath and this is known as a bleach-fix bath.

Most conventionally used bleach baths are based on alkali metal ferricyanide because it gives the fastest and most effective bleaching. However ferricyanides are not used in commercial bleach-fix baths; they tend to employ ferric ions co plexed with either ethylene- diaminetetracetic acid (EDTA) or nitrilotriacetic acrd (NTA) even though many other complexing agents have been proposed.

Ferric EDTA and NTA are not always suitable for bleach baths as they are slower than ferricyanide bleaches ^' and not sufficiently strong to oxidize some image dyes leaving them in their less strongly'coloured leuco form.

British Patent Specification 1,394,357 describes photographic bleach solutions which essentially contain a thioamide compound in addition to a ferric ion complex bleaching agent. On page 2 of the specification iminodi- acetic acid (IDA) is listed as a possible complexing agent for the ferric ions.

Bleach-fix baths are also widely used in photographic colpur processing and, as their name suggests, combine the functions of a bleach and a fix bath. German Patent Specification 866,605 (published in 1953) describes bleach-fix baths in which the bleaching agent is a ferric complex of an organic ^' acid of the general formula:

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or H00C-R ₄ -N-R ₃ -C00H

HOOC-R ₄ -N-R ₅ -COOH in which X represents

and , R and R^ represent hydrocarbon radicals which may be substituted and R may also represent hydrogen, and in which Ε.. , R,- and Rg represent bivalent hydrocarbon radicals which may again be substituted. Among the specific examples of such acids listed are EDTA, NTA and ethyliminodipropionic acid (EIDPA). Of all the organic acids specified in the German Specificati only EDTA has been widely used in practice. The acid EID is unattractive commercially as it is expensive to produc and not otherwise readily available.

There are environmental objections to both ferricyanides and ferric EDTA and NTA. ^' The decomposition products of ferricyanide wastes can be toxic especially to fish. EDTA and NTA, if discharged into some environ¬ ments which contain precipitated heavy metals, e.g. on se beds or in lakes, can redissolve these heavy metals. The metals are then able to enter the food chain of aquatic animals. The present invention,provides photographic bleach compositions _^ which are more active than ferric EDT NTA or IDA compositions and which are free from the envir mental and commercial objections to the photographic . bleaching agents mentioned above. According to the present invention, there is provided a photographic bleach composition which comprise

as bleaching agent a ferric complex of an alkyliminodi¬ acetic acid the alkyl group of which may be substituted.

Alkyliminodiacetic acids are available commercially but may be prepared cheaply and easily 5 by a method described for the preparation of methylimino- acetic acid (MIDA) -by G.J.Berchet.found in Blatt, Organic Synthesis, Vol. 11 397-398 which is described in Example 2 below.

The present invention further provides a 10 method of processing a photographic colour material which comprises the steps of bleaching the material containing both a silver image and a dye image with a bleach composition according to the present invention and either simultaneously or subsequently fixing the 15 material.

Any photographic silver halide ^' emulsions may be used in the materials to be processed with the present bleach compositions. These emulsions may comprise silver chloride, silver bromide, silver bro oiodide, silver

20 chlorobromide or mixtures thereof. Coarse grain or fine grain emulsions prepared by any of the well-known procedures may be used. The emulsions may contain any of the known chemical sensitizers, colour couplers, spectral sensitizers, antifoggants, stabilizers,- coating aids and

25 other addenda used in photographic materials. The silver halide emulsions may contain a hydrophilic colloid, for example, gelatin, gelatin derivatives, cellulose derivatives, polysaccharides such as dextrose or gum arabic, or synthetic polymeric substances, for example, the

^' 30 water-soluble polyvinyl compounds, poly(vinylpyrrolidone) and acrylamide polymers.

The alkyliminodiacetic acids which may be employed herein preferably have an alkyl group having 1-6 carbon atoms. The substituent on the alkyl group

3.5 (if present) may be, for example, a hydroxy group. Examples of particular alkyl and substituted alkyl groups which may

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be present on the alkyliminodiacetic acid are methyl, ethyl, n-propyl, n-butyl, n-amyl, hydroxyethyl and hydroxy-n-hexyl.

The ratio of alkyliminodiacetic acid to 5 ferric ions in the present compositions may vary widely, for example from 1:1 to 15:1 ^' , optimally from 1:1 to 5:1 on a molar basis.

The present bleach compositions may also contain other bleaching agents, for example, ferric

10 EDTA, or any of those listed in British Specification No. 1,340,131 or U.S. Patent No. 3,694,462, in addition to the bleaching agents specified above. The working strength bleach solutions may have a pH in the range 5 to 7 preferably pH 6.0 and will preferably contain -a

15 water-soluble halide, e.g., for colour films, potassium bromide in a concentration of more than 40 g litre, preferably from more than 60 g litre up to the limit of solubility.

The present bleach solutions are more effective

20. than ferric EDTA bleach solutions due to•the higher oxidation potential of the ferric alkyliminodiacetic acid complex. Consequently either faster bleaching can be obtained from an equivalent solution or equivalent bleaching c-an be obtained from a solution containing less

25 halide or bleaching agent. The present compositions may be stored in very concentrated solution, e.g. containing from up to 540 g/litre of bleaching agent, enabling kits of processing chemicals to be compact.

The present bleach solutions may contain 0 a silver halide solyent, preferably an ammonium or alkali metal thiosulphate, in which case they become bleach-fix solutions.

Other silver halide solvents which may be used include thiocyanates, .thioureas and thioethers, for exampl 5 those mentioned in British Specification 1,340,131.

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The following Examples illustrate the invention. Figures 1 to 4 of the accompanying drawings illustrate the results. Example 1 A series of bleach solutions was prepared according to the following formulations: 0.02M ferric chloride 0.1 M potassium bromide 0.25M alkyliminodiacetic acid The alkyl of the alkyliminodiacetic acid was methyl (MIDA), ethyl(EIDA), n-propyl (PIDA) or n-butyl (BIDA). These solutions were adjusted to pH 6.0 with ammonia and were used to bleach strips of exposed and developed medium speed black and white film, for varying times. After bleaching the strips were washed, fixed, washed and dried in the conventional manner. These strips were compared with strips bleached in a similar solution to the above except the alkyliminodiacetic acid was replaced with an equivalent molar concentration of EDTA. Pig. 1 shows the results. Example 2

To 2 moles of chloroacetic acid in 150 ml of water, were added 4 moles sodium hydroxide in 500 ml of water, the reaction mixture being cooled on ice and kept below 30°C. After this the ice bath was removed and 1 mole methyla ine (as 30 aqueous solution) was added slowly. The solution temperature was not allowed to rise above 50°C. No further purification of the MIDA is essential although for a commercial bleach the chloride should preferably be. removed*to prevent corrosion of equipment.

Half the solution prepared above was added slowly to 110 g hydrated ferric nitrate dissolved in small quantity of water. The solution was then buffered to pH _ 6.0 by adding ammonia solution. To this was added 50 g ammonium bromide and the solution was made up to 1 litre

with water.

This solution was used as bleach in the C-41 process described in the British Journal of Photography Annual 1977 pages 204-5 and compared to the bleach employed therein in the processing of sensitometrically exposed medium speed colour negative film. The control bleach had the formula:

EDTA PeNa 100 g

Potassium bromide 50 g Ammonia 20$ 6 ml

Water to make 1000 ml

(pH 5.9 - 6.1)

The results in the form of relative log exposu vs>. density through blue, green and red filters are ^* shown in Pig. 2. The two red filter curves are identical

No silver was detected by X-ray fluorescence in either sensitometric step wedges although ^' there is a slight increase in blue and green densities in the film bleached in iron (III) MIDA. Example 3

The photographic testing procedure of Example using a black and white microfilm,was repeated using a series of bleach solutions of the formula: 0.02M ferric chloride- 0.1 M potassium bromide

0.25M acid pH adjusted to 6.5 in which the acid was EDTA, NTA, IDA (iminodiacetic acid) (all comparative) or.MIDA (the invention). The results are shown in Figure 3. Example 4

The photographic testing procedure of Example was repeated except that the bleach and fix solutions wer replaced by a single bleach-fix solution of the formula:

0.25M ferric chloride 0.25M acid

0.62M ammonium thiosulphate pH adjusted to 6.8 in which the acid was EDTA (comparative) or MIDA ( ^' invention). The results are shown in Figure 4.

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