CA2437951A1 - Stabilized cd-4 one-part film developer concentrates - Google Patents
Stabilized cd-4 one-part film developer concentrates Download PDFInfo
- Publication number
- CA2437951A1 CA2437951A1 CA002437951A CA2437951A CA2437951A1 CA 2437951 A1 CA2437951 A1 CA 2437951A1 CA 002437951 A CA002437951 A CA 002437951A CA 2437951 A CA2437951 A CA 2437951A CA 2437951 A1 CA2437951 A1 CA 2437951A1
- Authority
- CA
- Canada
- Prior art keywords
- salt
- concentrate
- hydroxylamine
- composition
- part liquid
- 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.)
- Abandoned
Links
Landscapes
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Abstract
Photographic developer replenisher concentrates comprising more reactive developers, like 4(N-ethyl-N-2-hydroxyethyl)-2-methylphenylenediamine (CD-4) undergo rapid oxidation, and consequently, have shorten shelf-life stabilities. Hydroxylamine type derivatives, while disclosed as being useful as a class of antioxidants for stabilizing photographic developer replenishers, most were found to impart either inadequate shelf-life stability for CD-4 developer, or interfered with "satisfactory developer performance."
Surprisingly, it was discovered the shelf-life stability of replenisher concentrates comprising CD-4 photographic developer could be extended for periods of 2 years or longer, and also provide satisfactory developer performance when the hydroxylamine antioxidant comprises at least N,N-bis(2-sulfoethyl) hydroxylamine (SEHA) or a salt thereof.
Surprisingly, it was discovered the shelf-life stability of replenisher concentrates comprising CD-4 photographic developer could be extended for periods of 2 years or longer, and also provide satisfactory developer performance when the hydroxylamine antioxidant comprises at least N,N-bis(2-sulfoethyl) hydroxylamine (SEHA) or a salt thereof.
Description
TECHNICAL FIELD
The present invention relates in general to photographic development, and more particularly to compositions and methods of making concentrated replenishes compositions for color developing of photographic substrates, and especially photographic films, which concentrates possess improved shelf-life stability.
BACKGROUND OF THE INVENTION
In the processing of color films and papers the maintenance of developer activity is necessary for uniform development. In recent years, it has become the practice to introduce a replenishing solution to the developing solution in order to replace depleted chemicals and solution carried away. Unless this is done, there will be a depletion of active ingredients, and a build-up of reaction by-products formed as development progresses. Thus, the concentration of reaction by-products may in time exceed the concentration of the developing agent. As~the reaction by-products increase the probability of the developer agent being absorbed by the silver halide grain decreases, and the likelihood of uneven or incomplete development increases.
Accordingly, replenishment of developing solutions requires restoration of developing agents, preservatives, etc., since their concentrations normally fall in developing processes.
A wide range of photographic replenishers are known. One especially useful color developer replenishes concentrate composition is disclosed by Laszlo Papai in U.S. Pat. 5,891,609, which relates to one-part, multi-phase liquid concentrates comprising inter-alia a single ring heterocyclic amide solvent, such as e-caprolactam.
A further representative example of color developing replenishers is disclosed by Charles R. Darmon, et al in U. S .
- Pat. 6,017,687. The monophase solutions, however, require the developing agents to be exclusively in the free base form. The solutions do not employ developing agents customarily available in an acid salt form. The concentrates are featured for use in developing color paper substrates.
The Darmon et al patent discloses several embodiments of replenishing solutions for processing color paper substrates comprising a wide range of developing agents in free base form stabilized with a myriad of potentially useful antioxidants.
Included were the hydroxylamine type antioxidants. This inventor found that replenisher concentrates comprising 4(N-ethyl-N-2 hydroxyethyl)-2-methylphenylenediamine sulfate developing agent (also known as CD-4), was so sensitive to oxidation that stable concentrates with commercially acceptable, extended shelf-life, i.e., at least one year, could not be readily prepared with most of the antioxidants suggested by Darmon et al.
In particular, most hydroxylamine type derivatives, while disclosed by Darmon et al as being useful as a class of antioxidants for stabilizing photographic developer replenishers, were found to impart either inadequate shelf-life stability for more reactive type developers, like CD-4, or interfered with developer performance. That is, even those hydroxylamine type antioxidants which provided some improvement in shelf-life, often impaired satisfactory developer performance. Consequently, commercial development of one-part color film replenisher concentrates comprising more reactive CD-4 film developer has not been commercially successful.
Accordingly, it would be highly desirable to have a CD-4-containing one-part film developer concentrate for replenishing developing solutions for photographic film, wherein the concentrates possess extended shelf-life stability, i.e., at least about 12 months, and more preferably, from above about 12 to 24 months, or more, and not impede satisfactory film development. Such concentrates should be available either as a monophase or multiphase system and be suitable for use with CD-4 developing agents as mixtures which contain either the salt form of CD-4 or the free base.
DETAILED DESCRIPTION OF THE INVENTION
It is therefore a principle object of the invention to provide a series of one-part photographic replenisher concentrates with extended shelf-life stability, which are especially useful in development of color films, as well as photographic color papers.
Generally, the one-part liquid concentrated color developer replenisher concentrates of the invention are compositions comprising at least a CD-4 developing agent, namely a 4(N-ethyl-N-2-hydroxyethyl)-2-methylphenylenediamine sulfate as a free base or free base-salt combinations, and a sufficient amount of the specific hydroxylamine antioxidant suitable for extending the useful shelf-life of the composition, and do so without impairing "satisfactory developer performance."
For purposes of this invention the expression "satisfactory developer performance," as appearing in the specification and claims is intended to mean complete and balanced development of the full color dye image, at industry-standard processing conditions (time, temperature, agitation, etc.), to industry-norm statistical standards as measured by densitometric readings of processed control strips.
More specifically the expression "satisfactory developer performance" as appearing in the specification and claims is intended to mean complete and balanced development of the full color image to industry-norm statistical standards as measured by densitometric readings of processed control strips, to within 2 to 3 points of variation from corrected reference aims, including the parameter of base-plus-fog, or Dmin~
The antioxidant found to possess the desired properties for stabilizing CD-4 developer without impairing satisfactory developer performance comprises at least N,N-bis (2-sulfoethyl) hydroxylamine (SERA) or a salt thereof. Virtually any of the known commercially available salts of this hydroxylamine may be used.
Both the CD-4 (4(N-ethyl-N-2-hydroxyethyl)-2-methylhenylene-diamine sulfate)-containing developer and the specific hydroxylamine, generally known as SERA are known chemical compounds, commercially available through ordinary channels of commerce. Most CD-4 developer comprises a mixture of the free base and the sulfate salt thereof. SERA and methods of manufacture are disclosed, for example, in U.S. Pat. 5,646,327 (Burns et al) and published European patent application 0 761 647.
The hydroxylamine antioxidant is usually employed as the disodium salt of N,N-bis(2-sulfoethyl)hydroxylamine.
Surprisingly, the particular antioxidant employed herein was found to be unique for simultaneously extending the shelf life of the CD-4 containing developer replenisher concentrates, and providing satisfactory developer performance. This inventor found that SERA is capable of stabilizing concentrates of CD-4 developing agent for 24 months, and more, without engendering the formation of unacceptably high levels of Dmin dye density.
Related anti-oxidants did not provide equivalent results with the highly sensitive CD-4 developing agent.
It was also discovered that optionally other hydroxylamine antioxidants may be used in combination with the N,N-bis(2-sulfoethyl)hydroxylamine (SERA). In each case, however, such combinations are required to have present at least the SERA
hydroxylamine antioxidant, N,N-bis(2-sulfoethyl) hydroxylamine.
A representative example of a hydroxylamine combination would be the N,N-bis(2-sulfoethyl) hydroxylamine and diethylhydroxylamine (DEHA), or salts thereof. When DEHA is used in combination with SERA reduced amounts of DEHA are preferred to keep the Dmin "stain" down to acceptable levels.
The present invention relates in general to photographic development, and more particularly to compositions and methods of making concentrated replenishes compositions for color developing of photographic substrates, and especially photographic films, which concentrates possess improved shelf-life stability.
BACKGROUND OF THE INVENTION
In the processing of color films and papers the maintenance of developer activity is necessary for uniform development. In recent years, it has become the practice to introduce a replenishing solution to the developing solution in order to replace depleted chemicals and solution carried away. Unless this is done, there will be a depletion of active ingredients, and a build-up of reaction by-products formed as development progresses. Thus, the concentration of reaction by-products may in time exceed the concentration of the developing agent. As~the reaction by-products increase the probability of the developer agent being absorbed by the silver halide grain decreases, and the likelihood of uneven or incomplete development increases.
Accordingly, replenishment of developing solutions requires restoration of developing agents, preservatives, etc., since their concentrations normally fall in developing processes.
A wide range of photographic replenishers are known. One especially useful color developer replenishes concentrate composition is disclosed by Laszlo Papai in U.S. Pat. 5,891,609, which relates to one-part, multi-phase liquid concentrates comprising inter-alia a single ring heterocyclic amide solvent, such as e-caprolactam.
A further representative example of color developing replenishers is disclosed by Charles R. Darmon, et al in U. S .
- Pat. 6,017,687. The monophase solutions, however, require the developing agents to be exclusively in the free base form. The solutions do not employ developing agents customarily available in an acid salt form. The concentrates are featured for use in developing color paper substrates.
The Darmon et al patent discloses several embodiments of replenishing solutions for processing color paper substrates comprising a wide range of developing agents in free base form stabilized with a myriad of potentially useful antioxidants.
Included were the hydroxylamine type antioxidants. This inventor found that replenisher concentrates comprising 4(N-ethyl-N-2 hydroxyethyl)-2-methylphenylenediamine sulfate developing agent (also known as CD-4), was so sensitive to oxidation that stable concentrates with commercially acceptable, extended shelf-life, i.e., at least one year, could not be readily prepared with most of the antioxidants suggested by Darmon et al.
In particular, most hydroxylamine type derivatives, while disclosed by Darmon et al as being useful as a class of antioxidants for stabilizing photographic developer replenishers, were found to impart either inadequate shelf-life stability for more reactive type developers, like CD-4, or interfered with developer performance. That is, even those hydroxylamine type antioxidants which provided some improvement in shelf-life, often impaired satisfactory developer performance. Consequently, commercial development of one-part color film replenisher concentrates comprising more reactive CD-4 film developer has not been commercially successful.
Accordingly, it would be highly desirable to have a CD-4-containing one-part film developer concentrate for replenishing developing solutions for photographic film, wherein the concentrates possess extended shelf-life stability, i.e., at least about 12 months, and more preferably, from above about 12 to 24 months, or more, and not impede satisfactory film development. Such concentrates should be available either as a monophase or multiphase system and be suitable for use with CD-4 developing agents as mixtures which contain either the salt form of CD-4 or the free base.
DETAILED DESCRIPTION OF THE INVENTION
It is therefore a principle object of the invention to provide a series of one-part photographic replenisher concentrates with extended shelf-life stability, which are especially useful in development of color films, as well as photographic color papers.
Generally, the one-part liquid concentrated color developer replenisher concentrates of the invention are compositions comprising at least a CD-4 developing agent, namely a 4(N-ethyl-N-2-hydroxyethyl)-2-methylphenylenediamine sulfate as a free base or free base-salt combinations, and a sufficient amount of the specific hydroxylamine antioxidant suitable for extending the useful shelf-life of the composition, and do so without impairing "satisfactory developer performance."
For purposes of this invention the expression "satisfactory developer performance," as appearing in the specification and claims is intended to mean complete and balanced development of the full color dye image, at industry-standard processing conditions (time, temperature, agitation, etc.), to industry-norm statistical standards as measured by densitometric readings of processed control strips.
More specifically the expression "satisfactory developer performance" as appearing in the specification and claims is intended to mean complete and balanced development of the full color image to industry-norm statistical standards as measured by densitometric readings of processed control strips, to within 2 to 3 points of variation from corrected reference aims, including the parameter of base-plus-fog, or Dmin~
The antioxidant found to possess the desired properties for stabilizing CD-4 developer without impairing satisfactory developer performance comprises at least N,N-bis (2-sulfoethyl) hydroxylamine (SERA) or a salt thereof. Virtually any of the known commercially available salts of this hydroxylamine may be used.
Both the CD-4 (4(N-ethyl-N-2-hydroxyethyl)-2-methylhenylene-diamine sulfate)-containing developer and the specific hydroxylamine, generally known as SERA are known chemical compounds, commercially available through ordinary channels of commerce. Most CD-4 developer comprises a mixture of the free base and the sulfate salt thereof. SERA and methods of manufacture are disclosed, for example, in U.S. Pat. 5,646,327 (Burns et al) and published European patent application 0 761 647.
The hydroxylamine antioxidant is usually employed as the disodium salt of N,N-bis(2-sulfoethyl)hydroxylamine.
Surprisingly, the particular antioxidant employed herein was found to be unique for simultaneously extending the shelf life of the CD-4 containing developer replenisher concentrates, and providing satisfactory developer performance. This inventor found that SERA is capable of stabilizing concentrates of CD-4 developing agent for 24 months, and more, without engendering the formation of unacceptably high levels of Dmin dye density.
Related anti-oxidants did not provide equivalent results with the highly sensitive CD-4 developing agent.
It was also discovered that optionally other hydroxylamine antioxidants may be used in combination with the N,N-bis(2-sulfoethyl)hydroxylamine (SERA). In each case, however, such combinations are required to have present at least the SERA
hydroxylamine antioxidant, N,N-bis(2-sulfoethyl) hydroxylamine.
A representative example of a hydroxylamine combination would be the N,N-bis(2-sulfoethyl) hydroxylamine and diethylhydroxylamine (DEHA), or salts thereof. When DEHA is used in combination with SERA reduced amounts of DEHA are preferred to keep the Dmin "stain" down to acceptable levels.
It is still a further object of the invention to provide for one-part liquid concentrated color developer replenisher compositions with extended shelf-life stability comprising at least the CD-4 developing agent, containing 4(N-ethyl-N-2-hydroxyethyl)-2-methylphenylenediamine sulfate, a shelf-life extending amount of the hydroxylamine antioxidant, N,N-bis(2-sulfoethyl) hydroxylamine or a salt thereof; a buffer for maintaining the pH of the composition in a range from about 10 to about 12, and a photographically acceptable solvent system.
The buffer system and other components of the solutions may comprise any of the salts and solutions familiar among persons skilled in the art, and which are known to be compatible with other ingredients of the compositions. The solvent system is preferably an organic solvent system. Representative preferred organic solvents include the caprolactams, such as those disclosed by Laszlo Papai in U.S. Pat. 5,891,609, the contents of which are incorporated herein by reference. Various polyhydric alcohols, such as ethylene glycol, diethylene glycol may also be employed, such as those described in US Pat.
6,017,687, the contents of which are incorporated herein-by-reference.
The one-part developer concentrates may be prepared in monophase format using. the above mentioned polyhydric alcohols, for example, or in a multiphase system using such solvents as caprolactam.
The CD-4 developing agent is employed in the concentrates of this invention in a range generally from about 10 to about 100 g/L, and more specifically, from about 25 to about 75 g/L. The hydroxylamine antioxidant, N,N-bis(2-sulfoethyl) hydroxylamine or salt thereof can be employed in a range generally from about 5 to about 75 g/L. When used in combinations with other antioxidants, such as diethylhydroxylamine, the combined antioxidants may be used in a range from about 5 to about 75 g/L.
Useful buffers and other adjuvant ingredients may be included as taught by Papai in his U.S. Pat. 5,891,609.
The buffer system and other components of the solutions may comprise any of the salts and solutions familiar among persons skilled in the art, and which are known to be compatible with other ingredients of the compositions. The solvent system is preferably an organic solvent system. Representative preferred organic solvents include the caprolactams, such as those disclosed by Laszlo Papai in U.S. Pat. 5,891,609, the contents of which are incorporated herein by reference. Various polyhydric alcohols, such as ethylene glycol, diethylene glycol may also be employed, such as those described in US Pat.
6,017,687, the contents of which are incorporated herein-by-reference.
The one-part developer concentrates may be prepared in monophase format using. the above mentioned polyhydric alcohols, for example, or in a multiphase system using such solvents as caprolactam.
The CD-4 developing agent is employed in the concentrates of this invention in a range generally from about 10 to about 100 g/L, and more specifically, from about 25 to about 75 g/L. The hydroxylamine antioxidant, N,N-bis(2-sulfoethyl) hydroxylamine or salt thereof can be employed in a range generally from about 5 to about 75 g/L. When used in combinations with other antioxidants, such as diethylhydroxylamine, the combined antioxidants may be used in a range from about 5 to about 75 g/L.
Useful buffers and other adjuvant ingredients may be included as taught by Papai in his U.S. Pat. 5,891,609.
The color developing replenisher concentrates of this invention may be prepared using the following protocol:
The color developing agent (CD-4) is dissolved in an alkaline solution of potassium or sodium hydroxide, for example, and antioxidant/preservative, at least N,N-bis(2-sulfoethyl) hydroxyl-amine or a salt thereof (SERA), added thereto. The organic solvent, such as ethylene glycol, caprolactam, etc., is added to the alkaline-CD-4 antioxidant solution. In this solution, the salt of the CD-4 developer, such as the sulfate can be filtered out of the solution. To the filtrate, the other usual ingredients of the film developer, like sequestering agents, buffering agents, bromide salt, etc., are added.
If the organic solvent is a glycol or other polyhydric alcohol, a single or monophase developer is prepared. If the organic solvent is a caprolactam multiple distinct liquid phases are formed. The top layer is the organic solvent layer, whereas the bottom layer is the aqueous phase. By omitting a filtration step, a diphase or triphase developer concentrate depending on the organic solvent can also be prepared.
The invention also contemplates the use of CD-4 salt, and more preferably, the use of the CD-4 base. Use of the CD-4 base will eliminate the filtration step.
In order to demonstrate the invention, the following experiments were conducted:
For purposes of comparison a CD-4 developer replenisher concentrate was prepared with hydroxylamine sulfate (HAS), the traditional antioxidant used in mufti-part CD-4-containing developers:
Water............................800 ml KBr.............................Ø8 g/L
caprolactam.....................12.0 g/L
Potassium sulfite @ 690 g/L......8.33 ml/L
CD-4 developer...................5.6 g/L
Additional surfactant............3.0 ml/L
Hardness sequestrant.............1.0 ml/L
Potassium carbonate (800 g/L)...46.75 ml/L
HAS..............................2.8 g/L
Water to.........................1.0 L
pH..............................10.20 In the one-part developer environment of alkaline pH, the HAS decomposes, leaving no residual antioxidant to protect the highly reactive CD-4. This formula darkened in three days, an indicator that the CD-4 had decomposed, leaving insufficient active ingredient to provide satisfactory developer performance.
To demonstrate the performance of a one-part CD-4 developer replenisher concentrate stabilized with diethylhydroxylamine (DEHA) the following solution was prepared:
Water......................._..._800 ml KBR.............................Ø8 g/L
caprolactam.....................12.0 g/L~
Potassium metabisulfite..........2.9 g/L
Potassium sulfite @ 690 g/L......2.3 ml/L
CD-4 developer...................5.6 g/L
Additional surfactant............3.0 ml/L
Hardness sequestrant..............2.6 g/L
Potassium carbonate (800 g/L)....46.75 ml/L
DEHA (850)........................7.0 ml/L
Water to..........................1.0 L
pH...............................10.20 ~ 0.02 This solution was found to have a shelf life of about one year or less, based on elevated-temperature accelerated aging tests.
In addition, this developer solution preserved with DEHA only, did not provide satisfactory developer performance, in that it yielded a high Dmin densitometric result (high stain). This _7-example illustrates the sensitivity of the CD-4 developing agent to competing developer-acting compounds such as DEHA.
To further compare the performance of CD-4 developer replenisher stabilized with hydroxylamine antioxidant, a solution was prepared with SEHA disodium salt (sulfonatoethylhydroxylamine disodium salt, monohydrate) with the following formulation:
Water............................800 ml KBR.............................Ø8 g/L
caprolactam.....................12.0 g/L
Potassium metabisulfite..........4.0 g/L
CD-4 developer...................5.6 g/L
Hardness sequestrant.............2.6 g/L
KOH (500)..........................1.5 ml/L
Potassium carbonate (800 g/L).....46.75 ml/L
SEHA disodium (monohydrate).........5.0 g/L
Water to...........................1.0 L
pH.................................10.10 +/-0.05 This SEHA-only-preserved formula demonstrated a stable shelf life approaching two years, in elevated-temperature accelerated aging tests, and also provided satisfactory developer performance, in particular as regards stain, or Dmin, being kept at acceptably low levels.
Additionally, the stability and performance of CD-4 developer replenisher was tested using a combination o~f hydroxylamine antioxidants. A solution was prepared with SEHA
disodium salt (sulfonatoethylhydroxylamine disodium salt, monohydrate) and diethylhydroxylamine (DEHA) in the following formulation:
-g_ Water............................800 ml KBR.............................Ø8 g/L
caprolactam.....................12.0 g/L
Potassium metabisulfite..........4.0 g/L
CD-4 developer...................5.6 g/L
Hardness sequestrant.............2.6 g/L
KOH (500)........................1.5 ml/L
Potassium carbonate (800 g/L)...46.75 ml/L
SEHA disodium (monohydrate)......3.0 g/L
DEHA (850).......................3.0 ml/L
Water to.. .....................1.0 L
pH:.............................10.10 ~ 0.05 This combination SEHA-DEHA-preserved formula demonstrated a stable shelf life of greater than one year in elevated-temperature accelerated aging tests, and also provided satisfactory developer performance, in particular as regards stain, or Din, provided the DEHA level is kept sufficiently low as to stimulate its competing development activity in comparison to the CD-4 color developing agent.
The color developing agent (CD-4) is dissolved in an alkaline solution of potassium or sodium hydroxide, for example, and antioxidant/preservative, at least N,N-bis(2-sulfoethyl) hydroxyl-amine or a salt thereof (SERA), added thereto. The organic solvent, such as ethylene glycol, caprolactam, etc., is added to the alkaline-CD-4 antioxidant solution. In this solution, the salt of the CD-4 developer, such as the sulfate can be filtered out of the solution. To the filtrate, the other usual ingredients of the film developer, like sequestering agents, buffering agents, bromide salt, etc., are added.
If the organic solvent is a glycol or other polyhydric alcohol, a single or monophase developer is prepared. If the organic solvent is a caprolactam multiple distinct liquid phases are formed. The top layer is the organic solvent layer, whereas the bottom layer is the aqueous phase. By omitting a filtration step, a diphase or triphase developer concentrate depending on the organic solvent can also be prepared.
The invention also contemplates the use of CD-4 salt, and more preferably, the use of the CD-4 base. Use of the CD-4 base will eliminate the filtration step.
In order to demonstrate the invention, the following experiments were conducted:
For purposes of comparison a CD-4 developer replenisher concentrate was prepared with hydroxylamine sulfate (HAS), the traditional antioxidant used in mufti-part CD-4-containing developers:
Water............................800 ml KBr.............................Ø8 g/L
caprolactam.....................12.0 g/L
Potassium sulfite @ 690 g/L......8.33 ml/L
CD-4 developer...................5.6 g/L
Additional surfactant............3.0 ml/L
Hardness sequestrant.............1.0 ml/L
Potassium carbonate (800 g/L)...46.75 ml/L
HAS..............................2.8 g/L
Water to.........................1.0 L
pH..............................10.20 In the one-part developer environment of alkaline pH, the HAS decomposes, leaving no residual antioxidant to protect the highly reactive CD-4. This formula darkened in three days, an indicator that the CD-4 had decomposed, leaving insufficient active ingredient to provide satisfactory developer performance.
To demonstrate the performance of a one-part CD-4 developer replenisher concentrate stabilized with diethylhydroxylamine (DEHA) the following solution was prepared:
Water......................._..._800 ml KBR.............................Ø8 g/L
caprolactam.....................12.0 g/L~
Potassium metabisulfite..........2.9 g/L
Potassium sulfite @ 690 g/L......2.3 ml/L
CD-4 developer...................5.6 g/L
Additional surfactant............3.0 ml/L
Hardness sequestrant..............2.6 g/L
Potassium carbonate (800 g/L)....46.75 ml/L
DEHA (850)........................7.0 ml/L
Water to..........................1.0 L
pH...............................10.20 ~ 0.02 This solution was found to have a shelf life of about one year or less, based on elevated-temperature accelerated aging tests.
In addition, this developer solution preserved with DEHA only, did not provide satisfactory developer performance, in that it yielded a high Dmin densitometric result (high stain). This _7-example illustrates the sensitivity of the CD-4 developing agent to competing developer-acting compounds such as DEHA.
To further compare the performance of CD-4 developer replenisher stabilized with hydroxylamine antioxidant, a solution was prepared with SEHA disodium salt (sulfonatoethylhydroxylamine disodium salt, monohydrate) with the following formulation:
Water............................800 ml KBR.............................Ø8 g/L
caprolactam.....................12.0 g/L
Potassium metabisulfite..........4.0 g/L
CD-4 developer...................5.6 g/L
Hardness sequestrant.............2.6 g/L
KOH (500)..........................1.5 ml/L
Potassium carbonate (800 g/L).....46.75 ml/L
SEHA disodium (monohydrate).........5.0 g/L
Water to...........................1.0 L
pH.................................10.10 +/-0.05 This SEHA-only-preserved formula demonstrated a stable shelf life approaching two years, in elevated-temperature accelerated aging tests, and also provided satisfactory developer performance, in particular as regards stain, or Dmin, being kept at acceptably low levels.
Additionally, the stability and performance of CD-4 developer replenisher was tested using a combination o~f hydroxylamine antioxidants. A solution was prepared with SEHA
disodium salt (sulfonatoethylhydroxylamine disodium salt, monohydrate) and diethylhydroxylamine (DEHA) in the following formulation:
-g_ Water............................800 ml KBR.............................Ø8 g/L
caprolactam.....................12.0 g/L
Potassium metabisulfite..........4.0 g/L
CD-4 developer...................5.6 g/L
Hardness sequestrant.............2.6 g/L
KOH (500)........................1.5 ml/L
Potassium carbonate (800 g/L)...46.75 ml/L
SEHA disodium (monohydrate)......3.0 g/L
DEHA (850).......................3.0 ml/L
Water to.. .....................1.0 L
pH:.............................10.10 ~ 0.05 This combination SEHA-DEHA-preserved formula demonstrated a stable shelf life of greater than one year in elevated-temperature accelerated aging tests, and also provided satisfactory developer performance, in particular as regards stain, or Din, provided the DEHA level is kept sufficiently low as to stimulate its competing development activity in comparison to the CD-4 color developing agent.
Claims (19)
1. A one-part liquid concentrated color developer replenisher composition, characterized by comprising a 4(N-ethyl-N-2-hydroxyethyl)-2-methylphenylenediamine-containing developer, and a sufficient amount of a hydroxylamine antioxidant to extend the shelf-life of said composition comprising at least N,N-bis(2-sulfoethyl) hydroxylamine or a salt thereof, said composition further characterized by satisfactory developer performance.
2. The one-part liquid concentrate color developer replenisher composition of claim 1 characterized by the hydroxylamine antioxidant which is a disodium salt of N,N-bis(2-sulfoethyl) hydroxylamine.
3. The one-part liquid concentrate color developer replenisher composition of claim 1 characterized by the hydroxylamine antioxidant which comprises at least a salt of the N,N-bis(2-sulfoethyl) hydroxylamine in combination with at least one other hydroxylamine antioxidant.
4. The one-part liquid concentrate color developer replenisher composition of claim 3, characterized by the one other hydroxylamine antioxidant which is diethylhydroxylamine or a salt thereof.
5. The one-part liquid concentrate color developer replenisher composition of Claim 1 characterized wherein the developer is a member selected from the group consisting of 4(N-ethyl-N-2-hydroxyethyl)-2-methylphenylenediamine free base, a salt of 4(N-ethyl-N-2-hydroxyethyl)-2-methylphenylenediamine and mixtures thereof.
6. The one-part liquid concentrate color developer replenisher composition of Claim 1 characterized wherein the composition is a monophase concentrate.
7. The one-part liquid concentrate color developer replenisher composition of Claim 1 characterized wherein the composition is a multiphase concentrate.
8. A one-part liquid concentrated color developer replenisher composition, characterized by comprising a 4(N-ethyl-N-2-hydroxy-ethyl)-2-methylphenylenediamine-containing developer, a shelf-life extending amount of a hydroxylamine antioxidant comprising at least N,N-bis(2-sulfoethyl) hydroxylamine or a salt thereof;
a buffer for maintaining the pH of the composition in a range from about 10 to about 12, and a photographically acceptable solvent system, said composition further characterized by satisfactory developer performance.
a buffer for maintaining the pH of the composition in a range from about 10 to about 12, and a photographically acceptable solvent system, said composition further characterized by satisfactory developer performance.
9. The one-part liquid concentrated color developer replenisher composition of Claim 8 further characterized as a monophase concentrate.
10. The one-part liquid concentrated color developer replenisher composition of Claim 8 further characterized as a multiphase concentrate.
11. The one-part liquid concentrated color developer replenisher composition of Claim 9 characterized by the monophase concentrate which comprises a polyhydric alcohol.
12. The one-part liquid concentrated color developer replenisher composition of Claim 10 characterized by the multiphase concentrate which comprises an upper caprolactam-containing phase comprising the 4(N-ethyl-N-2-hydroxyethyl)-2-methylphenylene-diamine-containing developer and the N,N-bis(2-sulfoethyl) hydroxylamine antioxidant or salt thereof, and a lower aqueous phase comprising the buffer.
13. The one-part liquid concentrated color developer replenisher composition of Claim 12 characterized by the caprolactam-containing multiphase concentrate comprising a third phase in the form of a solid precipitate comprising a salt.
14. The one-part liquid concentrated color developer replenisher composition of Claim 8 characterized as a diphase concentrate comprising a polyhydric alcohol-containing liquid phase and a solid phase comprising a salt.
15. The one-part liquid concentrate color developer replenisher composition of Claim 8 characterized wherein the developer is a member selected from the group consisting of 4(N-ethyl-N-2-hydroxyethyl)-2-methylphenylenediamine free base, a salt of 4(N-ethyl-N-2-hydroxyethyl}-2-methylphenylenediamine and mixtures thereof.
16. A method far preparing a stabilized one-part liquid concentrated color developer replenisher composition, characterized by the steps which comprise (i) dissolving a 4(N-ethyl-N-2-hydroxyethyl)-2-methyl-phenylenediamine-containing developer in an alkaline solution comprising a base, and an antioxidant comprising at least N,N-bis(2-sulfoethyl)hydroxylamine or a salt thereof:
(ii) introducing a photographically compatible organic solvent, and (iii) introducing a buffering agent to maintain the pH of the solution in a range from about 14 to about 12, said composition further characterized by satisfactory developer performance.
(ii) introducing a photographically compatible organic solvent, and (iii) introducing a buffering agent to maintain the pH of the solution in a range from about 14 to about 12, said composition further characterized by satisfactory developer performance.
17. The method of Claim 16 characterized by the photographically compatible organic solvent which is a polyhydric alcohol, and the one-part liquid concentrated developer replenisher composition is a monophase concentrate, said method including the step of removing a salt precipitate.
18. The method of Claim 16 characterized by the photographically compatible organic solvent which is a polyhydric alcohol, and the developer concentrate is a diphase system comprising a liquid phase and a solid phase comprising a salt.
19. The method of Claim 16 characterized by the photographically compatible organic solvent which is a caprolactam forming a diphase system comprising an upper caprolactam-containing solvent and a lower aqueous phase, said method including the step of removing a salt.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26734701P | 2001-02-08 | 2001-02-08 | |
| US60/267,347 | 2001-02-08 | ||
| PCT/US2002/021652 WO2003003116A1 (en) | 2001-02-08 | 2002-02-06 | Stabilized cd-4 one-part film developer concentrates |
| USUNKNOWN | 2003-08-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2437951A1 true CA2437951A1 (en) | 2003-01-09 |
Family
ID=29250338
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002437951A Abandoned CA2437951A1 (en) | 2001-02-08 | 2002-02-06 | Stabilized cd-4 one-part film developer concentrates |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2437951A1 (en) |
-
2002
- 2002-02-06 CA CA002437951A patent/CA2437951A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0980024B1 (en) | Homogeneous single-part photographic color developing concentrate and method of making | |
| US6017687A (en) | Low replenishment color development using chloride ion-free color developer concentrate | |
| EP1099980B1 (en) | Calcium ion stable photographic color developing concentrate and method of manufacture | |
| US5891609A (en) | Photographic color developer replenishing concentrates | |
| US6416940B2 (en) | Calcium ion stable photographic color developing composition and method of use | |
| US2845349A (en) | Photographic developers | |
| US20020150845A1 (en) | Stabilized CD-4 one-part film developer concentrates | |
| US4298681A (en) | N,N Disubstituted p-phenylenediamine phosphates to form a color developer working solution, a color developer concentrate containing such a phosphate and a method of using said working solution for color development of color film | |
| CA2437951A1 (en) | Stabilized cd-4 one-part film developer concentrates | |
| US6770429B2 (en) | Single part color photographic developer concentrate | |
| JPH0410059B2 (en) | ||
| EP0118693A2 (en) | Photographic color developer composition packaged in two or more concentrated parts, particularly solutions, and concentrated color developer water solution | |
| US6599688B1 (en) | Stable photographic color developing composition and method of use | |
| EP1389743A1 (en) | Stable photographic color developing composition and method of use | |
| US6468724B2 (en) | Color photographic developer concentrate | |
| JPH023040A (en) | Color photographic developing agent | |
| US20060093970A1 (en) | Combinations of preservatives and sequestrants to avoid formation of isonitrile malodor | |
| JPH0452455B2 (en) | ||
| US20010041312A1 (en) | Photographic processing solutions | |
| EP1061416A1 (en) | Colour photographic developer concentrate |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued | ||
| FZDE | Discontinued |
Effective date: 20060206 |