Stabilized bleaching compositions and method of processing color elements

• US 6,077,650 A
• Filed: 06/28/1999
• Issued: 06/20/2000
• Est. Priority Date: 06/28/1999
• Status: Expired due to Fees

• Current Assignee: Eastman Kodak Company
• Original Assignee: Eastman Kodak Company
• Inventors: Price, Harry J.
• Primary Examiner(s): Le, Hoa Van
• Application Number:
  US09/340,876
• Time in Patent Office: 358 Days
• Field of Search: 430/461
• US Class Current: 430/461
• CPC Class Codes: G03C 5/44 Bleaching; Bleach-fixing
• CPC Class Codes: G03C 7/42 Bleach-fixing or agents therefor ; Desilvering processes
• CPC Class Codes: G03C 7/421 Additives other than bleaching or fixing agents

Abstract

Color photographic elements can be effectively processed to provide color images using biodegradable bleaching compositions in which the bleaching agent includes a pyridinecarboxylic acid or 2,6-pyridinedicarboxylic acid chelating ligand. The bleaching composition is stabilized by incorporation of an organic amine base instead of the conventional inorganic base.

Claims

1. A photographic bleaching composition comprising:

a) at least 0.01 mol/l of a bleaching agent that comprises ferric ion chelated with a first chelating ligand comprising an aromatic nitrogen heterocycle, and

b) at least 0.01 mol/l of an organic amine base,

said bleaching composition being substantially free of inorganic bases and the molar ratio of said organic amine base to said first chelating ligand being at least 1;

1, said organic amine base is ethanolamine, triethanolamine, ethylenediamine, diethylamine, triethylamine, morpholine, tetramethylethylenediamine, piperazine, diethanolamine or 2-methylaminoethanol.

2. The composition of claim 1 wherein said bleaching agent comprises ferric ion chelated only with said first chelating ligand.

3. The composition of claim 1 that is a bleach-fixing composition that further comprises a photographic fixing agent.

4. The composition of claim 1 wherein said first ligand is represented by the following structure I or II:

##STR6## wherein R, R'"'"', R" and R'"'"'" are independently hydrogen, a substituted or unsubstituted alkyl of 1 to 5 carbon atoms, substituted or unsubstituted aryl group of 6 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl of 5 to 10 carbon atoms, hydroxy, nitro, sulfo, amino, carboxy, sulfamoyl, sulfonamido, phospho or halo (such as chloro or bromo), or any two of R, R'"'"', R" and R'"'"'" can comprise the carbon atoms necessary to form a substituted or unsubstituted 5 to 7-membered ring fused with the pyridinyl nucleus.

5. The composition of claim 4 wherein R, R'"'"', R" and R'"'"'" are independently hydrogen, hydroxy or carboxy.

6. The composition of claim 1 wherein said first chelating ligand is unsubstituted 2-pyridinecarboxylic acid or 2,6-pyridinedicarboxylic acid.

7. The composition of claim 1 wherein said organic amine base has a water solubility of at least 0.01 mol/l.

8. The composition of claim 1 wherein said organic amine base is ethanolamine, diethanolamine or triethanolamine.

9. The composition of claim 8 wherein said organic amine base is ethanolamine.

10. The composition of claim 1 wherein said bleaching agent is present in an amount to provide ferric ions in an amount of from about 0.01 to about 1 mol/l, and said organic amine base is present in an amount of from about 0.01 to about 3 mol/l.

11. The composition of claim 1 further comprising rehalogenating agent or buffer, or both.

12. The composition of claim 1 wherein said bleaching agent comprises ferric ion chelated with said first chelating ligand and a second chelating ligand, the molar ratio of said first chelating ligand to ferric ion being from about 0.6:

1 to about 2;

1, and the molar ratio of said second chelating ligand to ferric ion being from about 0.2;

1 to about 2;

1.

13. The composition of claim 12 wherein said second chelating ligand is a biodegradable aminopolycarboxylic acid or polycarboxylic acid chelating ligand.

14. The composition of claim 13 wherein said second chelating ligand is an iminodiacetic acid or a derivative thereof, an aminodisuccinic acid, an aminomonosuccinic acid, alaninediacetic acid, β

-alaninediacetic acid, nitrilotriacetic acid, glycinesuccinic acid, 2-pyridylmethyliminodiacetic acid, tartaric acid or citric acid.

15. The composition of claim 13 wherein said second chelating ligand is represented by Structure III or IV:

##STR7## wherein m and n are independently 1, 2 or 3, R₁ is hydrogen, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group having from 5 to 10 carbon and heteroatoms, ##STR8## wherein p and q are independently 1, 2 and 3, the linking group X is any divalent group that does not bind ferric ion and does not cause the resulting ligand to be water-insoluble.

16. The composition of claim 15 wherein said second chelating ligand of Structure III is:

##STR9## and said second chelating ligand of Structure IV is;

##STR10##

17. The composition of claim 13 wherein said aminopolycarboxylic acid chelating ligand is methyliminodiacetic acid, iminodiacetic acid, ethyliminodiacetic acid or nitrilotriacetic acid.

20. A method of photographic processing comprising bleaching an imagewise exposed and color developed photographic silver halide element with the bleaching composition of claim 1.

21. The method of claim 20 wherein said photographic silver halide element is a color reversal photographic silver halide film.

18. A photographic bleaching composition comprising:

a) at least 0.1 mol/l of a bleaching agent that comprises ferric ion chelated with a first chelating ligand that is unsubstituted 2-pyridinecarboxylic acid or 2,6-pyridinedicarboxylic acid, and a second chelating ligand that is methyliminodiacetic acid or nitrilotriacetic acid, the molar ratio of said first chelating ligand to ferric ion being from about 0.8;

1 to about 2;

1, and the molar ratio of said second chelating ligand to ferric ion being from about 0.5;

1 to about 2;

1, and

b) at least 0.1 mol/l of ethanotamine, diethanolamine or triethanolamine, or a mixture of any of these,

said bleaching composition being substantially free of inorganic bases and the molar ratio of ethanolamine, diethanolamine or triethanolamine, or a mixture of any of these, to said second chelating ligand being at least 1;

1.

19. The composition of claim 18 wherein said second chelating ligand is nitrilotriacetic acid, and said organicamine base is ethanolamine.