EP0615633A1

EP0615633A1 - Developer solutions.

Info

Publication number: EP0615633A1
Application number: EP92924625A
Authority: EP
Inventors: Peter Jeffery Twist
Original assignee: Kodak Ltd; Eastman Kodak Co
Current assignee: Kodak Ltd; Eastman Kodak Co
Priority date: 1991-12-03
Filing date: 1992-11-30
Publication date: 1994-09-21
Anticipated expiration: 2012-11-30
Also published as: GB9125689D0; WO1993011460A1; EP0615633B1; DE69217557T2; DE69217557D1; JPH07502131A

Abstract

Solution d'amplification d'oxydoréduction comportant du peroxyde d'hydrogène ou une substance pouvant dégager du peroxyde d'hydrogène, ou bien un agent de réduction, par exemple un révélateur couleur, ainsi qu'au moins deux agents complexants associés l'un à l'autre et destinés à se complexer avec un ion d'élément de transition afin d'inhiber la catalyse des impuretés issues d'un enduit de pellicule photographique, et d'améliorer la stabilité de la solution; procédé de traitement photographique en couleurs comprenant l'utilisation de la solution d'amplification d'oxydoréduction; et son utlilisation à cette fin.Redox amplification solution comprising hydrogen peroxide or a substance which can release hydrogen peroxide, or else a reducing agent, for example a color developer, as well as at least two complexing agents combined with one the other and intended to complex with a transition element ion in order to inhibit the catalysis of impurities resulting from a coating of photographic film, and to improve the stability of the solution; a color photographic processing method comprising using the redox enhancement solution; and its use for this purpose.

Description

■ YF.VF.T.OPER SOLUTIONS

This invention relates to photographic developer solutions for use in photographic colour processing and in particular to redox developer solutions.

Redox (or RX) amplification processes have been described, for example, in British specification Nos 1,268,126, 1,399,481, 1,403,418 and 1,560,572. In such processes colour materials are developed to produce a silver image (which may contain only small amounts of silver) which then catalyses redox amplification to form a dye image. The redox amplifying solution contains a reducing agent, for example a colour developing agent, and an oxidising agent which is more powerful than silver halide and which will oxidise the colour developing agent in the presence of the silver image which acts as the catalyst. The oxidised colour developer reacts with a colour coupler (usually contained in the photographic material) to form image dye. The amount of dye formed depends on the time of treatment or the availability of colour coupler rather than the amount of silver in the image as is the case in conventional colour development processes. A particular application of this technology is in the processing of silver chloride colour paper, especially such paper with low silver levels.

Since the amplifying solution contains both an oxidising agent and a reducing agent it is, however, inherently unstable and will decompose on keeping. This instability is catalysed during the processing by the seasoning of species present in the gelatin layer in the photographic material, such as complex transition metal ions such as manganese (Mn) , and/or catechol disulphonate 'CDS¹, 'TIRON',T . In conventional RA-4 type developers this catalytic effect can be substantially reduced or nullified by the addition of one or more sequestering agents which can form a fairly stable soluble complex with the calcium ions or transition metal ions so that the free metal ions, especially ferric ions, are then present in only minute amounts. Such sequestering agents may include, for example, a polyacetic acid such as diethylaminetriamine pentaacetic acid 'DTPA¹ or an alkylidene -1,1-diphosphonic acid, such as 1-hydroxy- ethylidene-1,1-diphosphonic acid "HEPA* .

It is disclosed in co-pending U.K. application No. 9125687.5, filed on even date herewith, that a single sequestering agent but more particularly a combination of two or more sequestering agents can have a surprising stabilising effect in inhibiting catalytic decomposition of a photographic bleach solution.

It has now been found that in the redox developer field, whilst the addition of a single sequestering agent, such as 'DTPA* or a salt thereof, to a redox amplification solution has very little stabilising effect, the combination of two or more classes of sequestering agents may produce a synergistic effect, showing substantial inhibition of the catalytic effect caused by seasoning of the impurities inherent in or added to the photographic film coating. Moreover, the effect of this inhibition is greater than just the removal of the catalytic effect of, for example, Mn and/or 'CDS' and results unexpectedly in a significant improvement in the stability of RX developers compared to a control without species such as Mn and/or 'CDS'. Indeed the stability may be improved to an extent that the^' amount of Time Dependent Replenisher (TDR) normally needed to maintain such a solution in a satisfactory operating condition is significantly reduced, and may even be reduced to zero.

According to the present invention therefore there is provided a redox-amplification solution comprising hydrogen peroxide or a substance capable of releasing hydrogen peroxide, a reducing agent, such as a colour developing agent, and in combination two or more sequestering agents for complexing with a transition metal ion to inhibit catalysis of impurities emanating from a photographic film coating and enhance the stability of the solution.

One class of sequestering agent that is present according to the invention is a polyalkylcarboxylic, phosphonic or sulphonic acid containing at least one amine group which has condensed with one or more alkyl hydrogens of the alkylcarboxylic, phosphonic, or sulphonic-acid, which may be represented by the formula (I)

wherein X 1 and X2 may be the same or different and each is a hydrogen atom, a straight or branched chain alkyl group having

1 to 6 carbon atoms, a hydroxyl, carboxyl, sulphonyl or phosphonyl group or the group Z, wherein Z =

,0H

\

! ϋ

I a b

wherein a, b, c and d are the same or different and each is a hydrogen atom, a straight or branched chain alkyl group having

1 to 6 carbon atoms, a hydroxyl, carboxyl, -

1 sulphonyl or phosphonyl group or either X

2 and/or X may be repeat units of A or B, Y is as defined for a, b, c and d or is the group Z or the group B,

wherein X 3 and X4 are the same or different and are as defined for X 1 and X2 wherein the sum of , n and r is an integer from 1 to 10 and wherein one or both of the hydrogen atoms in each of the (CH2)m. (CH2)n or (CH2)r groups may be replaced by a straight or branched chain alkyl group having 1 to 6 carbon atoms, with the proviso that at least one of X 1, X2, X 3 and X4 is or contains a carboxylic, sulphonyl or phosphonyl group, or a salt thereof.

Examples of compounds of formula (I) that are particularly suitable are ethylenediaminetetraacetic acid ΕDTA', propylenediaminetetraacetic acid 'PDTA', nitrilotetraacetic acid *NTA' but most preferably diethylenetriaminepentaacetic acid 'DTPA', these compounds generally being used in the form of their corresponding tetra- or penta-sodium salts.

For the practice of the invention, in a preferred mode, a compound of formula (I) , or a salt thereof, is combined with either an alkylidene-1, 1- diphosphonic acid, such as a compound of formula (II) , as defined hereinbelow and/or a polyhydroxyl phenyl, such as a compound of formula (III) , as defined hereinbelow.

A compound of formula (II) is defined as

O X O

II I II

HO p c P OH (II₎

I I I OH (CH₂)_nH OH wherein X = a hydrogen atom or a halogen or hydroxyl group, n = 0 - 12 and especially 1-hydroxy-ethylidene-l,1- diphosphonicacid (X = OH; n = 1)

The compound of formula (III) is defined as

wherein R 1, R2, R3and R4 are the same or diffe-rent and each is a hydrogen atom, a straight or branched chain alkyl group having 1 to 6 carbon atoms, a hydroxyl, sulphonyl or carboxyl group. and is especially dihydroxyphenyl sulphonate ('catechol' disulphonate ^»CDS*) or 'TIRO ^• .

According to the present invention therefore in a preferred aspect there is provided a redox- amplification solution comprising hydrogen peroxide or a substance capable of releasing hydrogen peroxide, a reducing agent, such as a colour developing agent, and a compound of formula (I) , as hereinbefore defined, or a salt thereof, in combination with either a compound of formula (II) , as hereinbefore defined and/or a compound of formula (III) , as hereinbefore defined, for complexing with a transition metal ion to inhibit catalysis of impurities emanating from a photographic film coating and enhance the stability of the solution. In a more preferred aspect of the invention the redox-amplification solution comprises a compound of formula (I) , or a salt thereof, in combination with both a compound of formula (II) and a compound of formula (III) . Most preferably the redox-amplification solution comprises diethylenetriaminepentaacetic acid, 'DTPA* or a salt thereof and l-hydroxy-ethylidene-1,1- diphosphonic acid, 'HEPA'

These sequestering agents may be combined with the ratio of a y two components being in the range 1:1 to 20:1 by volume, wherein either component may be present in the greater amount. Each sequestering agent is added in an amount of from .05ml to lOOml/litre of redox solution, preferably 1ml to 10ml, most preferably 2ml to 6.5ml. Compounds capable of releasing hydrogen peroxide include metal peroxides; compounds which include hydrogen peroxide in their crystal structure such as sodium percarbonate; other peroxy compounds such as sodium perborate and persulphate; or soluble organic peroxides, such as butyl peroxide or benzyl peroxide.

The hydrogen peroxide or a compound such as mentioned above is added in a sufficient quantity to oxidise the colour developing agent in a suitable length of time. Conveniently commercially available 30% hydrogen peroxide is used in an amount of from 0.5 to lOOml/litre amplification bath, preferably about 5ml/litre, but equivalent amounts of, for example, 8% or 3% hydrogen peroxide may also be used. The reducing agent, which is generally a colour developing agent, may be any primary aromatic amine, such as a p-aminophenol or p-phenylenediamine. Colour developing agents which can be used include 4-amino-N,N-diethylaniline hydrochloride, 4-amino-3- methyl-N,N-diethylaniline hydrochloride, 4-amino-3- methyl-N-ethyl-N-β-hydroxyethylaniline sulphate and preferably N-ethyl-N-β-methanesulphon-amidoethyl-3- methyl-4-aminoaniline (CD3) .

The reducing agent is added in an amount of from about 1 to 20 g/litre, preferably 2 to 5 g/litre. The redox amplification solution preferably has one or more acids, alkalis or buffers , such as an alkali metal carbonate, carbonate/hydrogen carbonate buffer or phosphate buffer to maintain the pH at the required level, which is usually at about pH 10. The solution must be well buffered to provide a large reservoir of hydroxyl ions as a hydrogen ion is produced for each atom of metallic silver formed. As the pH rises the colour developing agent becomes a more powerful reducing agent with respect to the silver and therefore there is a higher rate of photographic development. However a high pH makes the developer more susceptible to aerial oxidation and hence more developing agent or protection from oxygen is required. Conveniently an anti-oxidant such as diethylhydroxylamine may be used.

The redox amplification solutions of the present invention may be used with any type of photographic silver halide colour material. Such materials and their possible constituents are described, for example, in Research Disclosure Item 308119, December 1989, published by Kenneth Mason Publications, Emsworth, Hants, United Kingdom. However materials based on predominantly silver chloride emulsions are preferred.

The present invention also provides a method of photographic colour processing including a redox amplification step, which comprises the addition of hydrogen peroxide, or a compound capable of releasing hydrogen peroxide, a reducing agent, such as a colour developing agent, a compound formula (I) , as hereinbefore defined, with either a compound of formula (II) , as hereinbefore defined and/or a compound of formula (III) as hereinbefore defined, for complexing with a transition metal ion to inhibit catalysis of impurities emanating from a photographic film coating and enhance the stability of the solution.

The redox amplification stage may be followed directly by a bleach step or an intermediate stop bath may be employed. The photographic material to be processed preferably contains low levels of silver to reduce light scattering and is preferably based on emulsions which comprise at least 80%, preferably at leat 90%, silver chloride and especially substantially pure silver chloride.

The invention will now be described with reference to the following examples which in no way limit the scope of the invention.

Example 1

A developer-amplifier (DEVAMP) of the following composition was prepared:-

Component Concentration Potassium carbonate 10.0 g/1

Potassium bromide 1.0 mg/1

Potassium chloride 0.35 g/1

Diethylhydroxylamine 4.0 ml/1 (anti-oxidant) CD3(colour developing 3.5 g/1 agent)

H2O2 (30%) 5.0 ml/1 pH 10.3

Temperature 35°C

A solution of each of the following in tap water containing approximately 200 ppm of equivalent calcium carbonate was prepared and transferred to glass cylinders maintained at 35°C in a water thermostat. 1 The solution as above

+ 0.6 g/1 of a 60% solution in water of 1- hydroxy-ethylidene-1,-1-diphosphonic acid

^•HEPA¹

2 1 + 6.5 ml/1 of a 40% solution in water of the penta-sodium salt of diethylenetriaminepentaacetic acid 'DTPA' 3 1 + 5 ppm manganese (as manganese sulphate) + 0.5 g/1 catechol disulphonate 'CDS'

4 2 + 5 ppm Mn + 0.5 g/1 'CDS'

5 The solution as above + 6.5 ml/1 40% solution in water of the penta-sodium salt of 'DTPA'

6 5 + 5 ppm Mn + 0.5 g/1 'CDS¹

Small strips of exposed photographic paper were processed from time to time to monitor the activity of the DEVAMP solution.

The results of the stability test in terms of red Dmax reflection density for a neutral exposure are shown graphically in Figure 1.

The stability of solution 1, with sequestrant 'HEPA' only declined steadily, losing 20% Dmax in 1.5 hours and similarly solution 5 with sequestrant 'DTPA' only fell to less than 50% Dmax in the first 2 hours. The Dmax of solution 3 fell even more sharply, losing its activity entirely in about 20 minutes. However, no apparent stability loss occurred for over 3 hours with solutions 2, 4 and 6, with solution 4 surprisingly being the most stable and retaining 80% activity even after 7.5 hours, solution 2 having tailed off to 50% activity after this time and solution 6 retaining 85% after 5 hours.

Similar results were found for green and blue Dmax and these are shown in Figures 2 and 3 respectively, results for green Dmax mirroring these for red Dmax and those for blue Dmax showing a similar trend except that there was an unexpected upsurge in activity after 6 hours with solution 4 close to maximum activity after 7.5 hours.These results clearly show that when 'DTPA' is present in combination with either ^•HEPA¹ (solution 2) or 'CDS' (solution 6) a significant improvement in stability results, which is not found with a solution containing both 'HEPA' and 'CDS' with no 'DTPA' (solution 3) . However, the most stable

DEVAMP solution is one in which 'DTPA', 'HEPA' .and

^•CDS' are all present (solution 4).

Example 2

A developer-amplifier of the composition shown in Example 1 was prepared and a solution of each of the following in tap water containing approximately 200ppm of equivalent calcium carbonate prepared and transferred to glass cylinders maintained at 35°C in a water thermostat.

1. Solution 1 as in Example 1, including 0.6 g/1 of a 60% solution in water of 'HEPA' 2. 1 + 2ml/l 'DTPA'

3. 1 + 4ml/l 'DTPA'

4. 1 + 6.5ml/l 'DTPA¹

5. 4 + lOppm manganese (as manganese sulphate) + 0.6g/l 'CDS'.

In the above solutions 2-4, the 'DTPA' is used in the form of a 40% solution of its penta-sodium salt.

As before, small strips of exposed photographic paper were processed from time to time over a total of 7.5 hours to monitor the stability effect of the 'DTPA', and Mn/'CDS'.

The results of the stability test in terms of red Dmax reflection density for a neutral exposure are shown graphically in Figure 4.

The stability of solution 1, deteriorated steadily from the start, losing 20% Dmax in less than 2 hours, thence declining rapidly to 30% of the original after 7.5 hours. There was only insignificant stability loss with solutions 2-5 until 4 hours had elapsed, whereupon each solution then declined to 65%, 62%, 55% and 69% respectively after 7.5 hours. It will be noted that in this instance the most enhanced stability was found with the least amount of 'DTPA' showing the surprisingly small quantity of 'DTPA' required to provide a significant increase in stability, in the presence of 'HEPA' . As with Example 1 however, unexpectedly the addition of Mn/'CDS* provided an even better result despite the recognised disadvantageous catalysis normally associated with those impurities in the absence of 'DTPA', indicating the optimum result is obtainable with all three sequestering agents present.

In a similar experiment for blue Dmax the results are depicted graphically in Figure 5. Again solution 1 was the least stable falling to 54% after the end of the monitoring but in this instance no significant difference was observed between solutions 2, 3 and 4, all having declined to only about 75% at the end of the period. Once more solution 5 proved to have the greatest stability, falling only insignificantly to 88% even after 7.5 hours. Example. 3

A similar experiment was set up to try and establish whether it was the Mn or *CDS', in combination with the 'DTPA' and 'HEPA' that was primarily responsible for the unexpected enhancement in stability in comparing solutions 2 and 4 of Figure 1. The solutions tested for stability in terms of red Dmax reflection were 1. The solution as in Example 1 + 0.6 g/1 60% solution in water of 'HEPA' + 2 m/1 of a 40% solution of the penta-sodium salt of 'DTPA' 2. 1 + 'CDS' (0.6g/l)

3. 1 + 'CDS' (0.6g/l) + 2.5ppm Mn

4. 1 + 'CDS' (0.6g/l) + lOppm Mn

5. 1 + 2.5ppm Mn 6. 1 + lOppm Mn

The results, which are shown graphically in Figure 6, show that there is no significant decline in stability for any of the solutions until after 5 hours have elapsed. Thereafter those solutions containing Mn but no 'CDS' mirrored closely solution 1 falling to just below 60% after 8 hours, whereas those to which 'CDS* but no Mn had been added retained 85% stability after this time. These results show that it is the presence of the 'CDS' 'impurity', artificially added to the gelatin layer in the photographic material, together with the 'DTPA' and 'HEPA' that is apparently responsible, for the surprisingly high stability of solutions containing 'DTPA', 'HEPA' and 'CDS'/Mn.

Claims

CLAIMS.

1. A redox-amplification solution comprising hydrogen peroxide, or a substance capable of releasing hydrogen peroxide, a reducing agent, such as a colour developing agent, and in combination two or more sequestering agents for complexing with a transition metal ion to inhibit catalysis of impurities emanating from a photographic film coating and enhance the stability of the solution.

2. A redox-amplification solution as claimed in claim 1 comprising a compound of formula (I) ,

1 to 6 carbon atoms, a hydroxyl, carboxyl, sulphonyl or phosphonyl group or the group Z,

wherein Z =

wherein a, b, c ard d are the same or different and each is a hydrogen atom, a straight or branched chain alkyl group having 1 to 6 carbon atoms, a hydroxyl, carboxyl,

5 sulphonyl or phosphonyl group or either X 1 and/or X2 may be repeat units of A or B,

Y is as defined for a, b, c and d or is the group Z or the group B,

10

20 wherein X 3 and X4 are the same or different and are as defined for X 1 and X2 wherein the sum of m, n and r is an integer from 1 to 10 and wherein one or both of the hydrogen atoms in

25 each of the (CH2)m. (CH2)n or (CH2)r groups may be replaced by a straight or branched chain alkyl group having 1 to 6 carbon atoms, with the proviso that at least one of X 1, X2, X 3 and X4 is or contains a carboxylic,

30 sulphonyl or phosphonyl group or a salt thereof, in combination with either a compound of formula (II)

wherein X is a hydrogen atom, a halogen atom or a hydroxyl group, n is 0 -12, and/or a compound of formula (III)

OH

^ OH

II (III)

.3/ \ / \_R1

R2

wherein R 1, R2, R3and R4 are the same or different and each is a hydrogen atom, a straight or branched chain alkyl group having 1 to 6 carbon atoms, a hydroxyl, sulphonyl or carboxyl group.

3. A redox-amplification solution as claimed in Claim 2, comprising in combination a compound of formula (I),, or a salt thereof, a compound of formula (II) and a compound of formula (III) .

4. A redox-amplification solution as claimed in either of claims 2 and 3, comprising a compound of formula (I,) wherein at least one of X 1, X2, X3 and X4 is a carboxylic acid group.

5. A redox-amplification solution as claimed in any one of the claims 2 to 4, wherein the compound of formula (I) is diethylenetriaminepentaacetic acid, or a salt thereof.

6. A redox-amplification solution as- claimed in any one of claims 2 to 4, wherein the compound of formula (I) is ethylenediaminetetraacetic acid, or a salt thereof.

7. A redox-amplification solution as claimed in any one of claims 2 to 4, wherein the compound of formula (I) is propylenediaminetetraacetic acid, or a salt thereof.

8. A redox-amplification solution as claimed in any one of claims 2 to 4, wherein the compound of formula (I) is nitrilotetraacetic acid, or a salt thereof.

9. A redox-amplification solution as claimed in either of claims 2 and 3, wherein the compound of formula (II) is 1-hydroxy-ethylidene-l,1-diphosphonic acid.

10. A redox-amplification solution as claimed in either of claims 2 and 3, wherein the compound of formula (III) is dihydroxyphenyl sulphonate.

11. A redox-amplification solution as claimed in any one of claims 1 to 5, 9 and 10, comprising in combination, diethylenetriaminepentaacetic acid, or a salt thereof, 1-hydroxy-ethylidene-l,1-diphosphonic acid and dihydroxyphenyl sulphonate.

12. A redox-amplification solution as claimed in any one of the preceding claims, wherein the ratio of any two components is in the range 1:1 to 20:1 by volume, wherein either component may be present in the greater amount.

13. A redox-amplification solution as claimed in any one of the preceding claims, wherein each compound is added in an amount of from .05 ml to 100 ml/litre of redox-amplification solution.

14. A redox-amplification solution as claimed in claim 13, wherein the amount of each compound is from 2 ml to 6.5 ml.

15. A redox-amplification solution as claimed in any one of the preceding claims, wherein 30% hydrogen peroxide is used in an amount of from 0.5 to 100 ml/litre, preferably about 5 ml/litre of solution.

16. A redox-amplification solution as claimed in any one of the preceding claims, wherein the reducing agent is N-ethyl-N-β-methanesulphon- amidoethyl-3-methyl-4-amino-aniline.

17. A redox-amplification solution as claimed in any one of the preceding claims, wherein the reducing agent is added in an amount of from about 1 to 20 g/litre, preferably 2 to 5 g/litre.

18. A method of photographic colour processing including a redox amplification step which comprises the addition of hydrogen peroxide, or a compound capable of releasing hydrogen peroxide, a reducing agent, such as a colour developing agent, and in combinatio two or more sequestering agents for complexing with a transition metal ion to inhibit catalysis of impurities emanating from a photographic film coating and enhance the stability of the solution.

19. A method as claimed in claim 18, wherein the redox-amplification solution is as claimed in any one of Claims 1 to 17.

20. The use of a redox-amplification solution as claimed in any one of claims 1 to 17 in a method of photographic colour processing as claimed in claim 18.