← Back to Patent Explorer
US5093227A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for processing silver halide color photographic material

Assignee: Fujifilm Holdings Corp
•
Filing: 1989-10-03
•
Granted: 1992-03-03
•
Expires: 2009-10-03
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract There is disclosed a method for processing a silver halide color photographic material with a color developer containing at least one aromatic primary amine color-developing agent. In the method a silver halide color photographic material which comprises a pyrazoloazole-type coupler and an image-dye stabilizer, and has at least one of the layers comprising a silver halide emulsion of a high silver chloride and the total coating amount of silver of 0.75 g/m 2 or below is processed, after exposure to light, with a color developer containing a specified amount of chloride ions and bromide ions, to improve development treatment characteristics, desilvering ability, and stability of an image.

Inventors

  • 👤 Kiyoshi Nakazyo
  • 👤 Kazuaki Yoshida

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-09 13:34
CPC Classifications
G; G03; G03C; G03C7/00; G03C7/30; G03C7/3003; G03C7/3005; G03C7/3008; G03C7/301; G03C7/407; G03C7/413; G03C7/3022; G03C2007/3025; G03C7/32; G03C7/36; G03C7/38; Y; Y10; Y10S; Y10S430/00; Y10S430/164

Claims Analysis

Total Claims: 14
Claim 1
Independent Claim 823 words
A method for processing an imagewise exposed silver halide color photographic material with a color developer containing at least one aromatic primary amine color developing agent, comprising: providing as said silver halide color photographic material a material which contains at least one silver halide emulsion layer, said silver halide emulsion layer containing at least one pyrazoloazole coupler represented by the following formula (A): Formula (A) ##STR136## wherein R represents a hydrogen atom or a substituent, X represents a hydrogen atom or a group that can split off in a coupling reaction with an oxidized product of an aromatic primary amine developing agent, Za, Zb, and Zc each represent methine, substituted methine, ═N--, or --NH--, one of the Za--Zb bond and the Zb--Zc bond is a double bond, and the other is a single bond, and when Zb--Zc is a carbon-carbon double bond, the double bond may be part of the aromatic ring, a dimer or higher polymer may be formed through R or X, and when Za, Zb, or Zc is a substituted methine, a dimer or higher polymer may be formed through the substituted methine, said material further containing at least one compound represented by the following formula (I-a) or (III-a), wherein the compound represented by formula (I-a) is a compound that reacts with p-anisidine at the second-order reaction-specific rate k 2 (80° C.) of 1×10 -1 to 1×10 -5 l/mol.sec.: Formula (I-a) ##STR137## wherein R 1 represents an aliphatic group, an aromatic group, or a heterocyclic group; Link represents a single bond or --O--; Ar has the same meaning as that of the aromatic group defined for R 1 , except those that will react with the aromatic amine color developing agent to release a group useful as a reducer for photography, Formula (III-a) ##STR138## wherein M represents an atom or a radical that will form an inorganic salt or ##STR139## in which R 15 and R 16 , which may be the same or different, each represent a hydrogen atom, an aliphatic group, an aromatic group, or a heterocyclic group, R 15 and R 16 may be bond together to form a 5- to 7-membered ring, R 17 , R 18 , R 20 and R 21 , which may be the same or different, each represents a hydrogen atom, an aliphatic group, a heterocyclic group, an acyl group, an alkoxycarbonyl group, a sulfonyl group, a ureido group, or a urethane group, provided that at least one of R 17 and R 18 and at least one of R 20 and R 21 each is a hydrogen atom, R 19 and R 22 each represent a hydrogen atom, an aliphatic group, an aromatic group, or a heterocyclic group, R 19 may represent an alkylamino group, an arylamino group, an alkoxy group, an aryloxy group, an acyl group, an alkoxycarbonyl group, or an aryloxycarbonyl group, at least two of R 17 , R 18 , and R 19 may bond together to form a 5- to 7-membered ring, at least two of R 20 , R 21 , and R 22 may bond together to form a 5- to 7-membered ring, R 23 represents a hydrogen atom, an aliphatic group, an aromatic group, or a heterocyclic group, R 24 represents a hydrogen atom, an aliphatic group, an aromatic group, a halogen atom, an acyloxy group, or a sulfonyl group, and R 25 represents a hydrogen atom or a hydrolyzable group; R 10 , R 11 , R 12 , R 13 , and R 14 , which may be the same or different, each represent a hydrogen atom, an aliphatic group, an aromatic group, a heterocyclic group, a halogen atom, --SR 26 , --OR 26 , ##STR140## an aryloxycarbonyl group, a sulfonyl group, a a sulfonamide group, a sulfamoyl group, a ureido group, a urethane group, a carbamoyl group, a sulfo group, a carboxyl group, a nitro group, a cyano group, an alkoxalyl group, an aryloxalyl group, a sulfonyl group ##STR141## or a formyl group, in which R 26 and R 27 , which may be the same or different, each represent a hydrogen atom, an aliphatic group, an aromatic group, an acyl group, or a sulfonyl group, and R 28 and R 29 , which may be the same or different, each represent a hydrogen atom, an aliphatic group, an aromatic group, an alkoxy group, or an aryloxy group, said at least one silver halide emulsion layer containing said coupler represented by formula (A) comprising 80 mol % or over of silver chloride and the total coating amount of silver in the material is 0.75 g/m 2 or below; and developing said material, after it has been image exposed, with a color developer which contains chlorine ions in an amount of 3.5×10 -2 to 1.5×10 -1 mol/l, bromine ions in an amount of 3.0×10 -5 to 1.0×10 -3 mol/l, and said at least one aromatic primary amine color developing agent.
Claim 2
Independent Claim 823 words
A method for processing an imagewise exposed silver halide color photographic material with a color developer containing at least one aromatic primary amine color developing agent, comprising: providing as said silver halide color photographic material a material which contains at least one silver halide emulsion layer, said silver halide emulsion layer containing at least one pyrazoloazole coupler represented by the following formula (A): Formula (A) ##STR136## wherein R represents a hydrogen atom or a substituent, X represents a hydrogen atom or a group that can split off in a coupling reaction with an oxidized product of an aromatic primary amine developing agent, Za, Zb, and Zc each represent methine, substituted methine, ═N--, or --NH--, one of the Za--Zb bond and the Zb--Zc bond is a double bond, and the other is a single bond, and when Zb--Zc is a carbon-carbon double bond, the double bond may be part of the aromatic ring, a dimer or higher polymer may be formed through R or X, and when Za, Zb, or Zc is a substituted methine, a dimer or higher polymer may be formed through the substituted methine, said material further containing at least one compound represented by the following formula (I-a) or (III-a), wherein the compound represented by formula (I-a) is a compound that reacts with p-anisidine at the second-order reaction-specific rate k 2 (80° C.) of 1×10 -1 to 1×10 -5 l/mol.sec.: Formula (I-a) ##STR137## wherein R 1 represents an aliphatic group, an aromatic group, or a heterocyclic group; Link represents a single bond or --O--; Ar has the same meaning as that of the aromatic group defined for R 1 , except those that will react with the aromatic amine color developing agent to release a group useful as a reducer for photography, Formula (III-a) ##STR138## wherein M represents an atom or a radical that will form an inorganic salt or ##STR139## in which R 15 and R 16 , which may be the same or different, each represent a hydrogen atom, an aliphatic group, an aromatic group, or a heterocyclic group, R 15 and R 16 may be bond together to form a 5- to 7-membered ring, R 17 , R 18 , R 20 and R 21 , which may be the same or different, each represents a hydrogen atom, an aliphatic group, a heterocyclic group, an acyl group, an alkoxycarbonyl group, a sulfonyl group, a ureido group, or a urethane group, provided that at least one of R 17 and R 18 and at least one of R 20 and R 21 each is a hydrogen atom, R 19 and R 22 each represent a hydrogen atom, an aliphatic group, an aromatic group, or a heterocyclic group, R 19 may represent an alkylamino group, an arylamino group, an alkoxy group, an aryloxy group, an acyl group, an alkoxycarbonyl group, or an aryloxycarbonyl group, at least two of R 17 , R 18 , and R 19 may bond together to form a 5- to 7-membered ring, at least two of R 20 , R 21 , and R 22 may bond together to form a 5- to 7-membered ring, R 23 represents a hydrogen atom, an aliphatic group, an aromatic group, or a heterocyclic group, R 24 represents a hydrogen atom, an aliphatic group, an aromatic group, a halogen atom, an acyloxy group, or a sulfonyl group, and R 25 represents a hydrogen atom or a hydrolyzable group; R 10 , R 11 , R 12 , R 13 , and R 14 , which may be the same or different, each represent a hydrogen atom, an aliphatic group, an aromatic group, a heterocyclic group, a halogen atom, --SR 26 , --OR 26 , ##STR140## an aryloxycarbonyl group, a sulfonyl group, a a sulfonamide group, a sulfamoyl group, a ureido group, a urethane group, a carbamoyl group, a sulfo group, a carboxyl group, a nitro group, a cyano group, an alkoxalyl group, an aryloxalyl group, a sulfonyl group ##STR141## or a formyl group, in which R 26 and R 27 , which may be the same or different, each represent a hydrogen atom, an aliphatic group, an aromatic group, an acyl group, or a sulfonyl group, and R 28 and R 29 , which may be the same or different, each represent a hydrogen atom, an aliphatic group, an aromatic group, an alkoxy group, or an aryloxy group, said at least one silver halide emulsion layer containing said coupler represented by formula (A) comprising 80 mol % or over of silver chloride and the total coating amount of silver in the material is 0.75 g/m 2 or below; and developing said material, after it has been image exposed, with a color developer which contains chlorine ions in an amount of 3.5×10 -2 to 1.5×10 -1 mol/l, bromine ions in an amount of 3.0×10 -5 to 1.0×10 -3 mol/l, and said at least one aromatic primary amine color developing agent.
Claim 3
Dependent Claim 29 words
The method as claimed in claim 1, wherein the coupler represented by formula (A) is selected from the group consisting of 1H-imidazo[1,2-b]pyrazoles, 1H-pyrazolo[1,5-b]pyrazoles, 1H-pyrazolo[5,1-c][1,2,4]triazoles, 1H-pyrazolo[1,5-b][1,2,4]triazoles, 1H-pyrazolo[1,5-b]tetrazoles, and 1H-pyrazolo [1,5a]benzimidazoles.
Claim 4
Dependent Claim 32 words
The method as claimed in claim 1, wherein the amount of the coupler represented by formula (A) is 2×10 -3 to 5×10 -1 mol per mol of silver in the emulsion layer.
Claim 5
Dependent Claim 27 words
The method as claimed in claim 1, wherein the silver halide emulsion layer containing a coupler represented by formula (A) is a green-sensitive emulsion layer comprising high-silver-halide.
Claim 6
Dependent Claim 29 words
The method as claimed in claim 1, wherein the compounds represented by formula (III-a) have a second-order reaction-specific rate k 2 (80° C.) with p-anisidine of 1.0×1×10 -5 l/mol.sec.
Claim 7
Dependent Claim 25 words
The method as claimed in claim 1, wherein the compound represented by formula (I-a) is used in combination with the compound represented by formula (III-a).
Claim 8
Dependent Claim 33 words
The method as claimed in claim 1, wherein the compound represented by formula (I-a) or (III-a) is added to a hydrophilic colloid layer of the photographic material when the photographic material is produced.
Claim 9
Dependent Claim 35 words
The method as claimed in claim 1, wherein the compound represented by formula (I-a) or (III-a) is used with a coupler in an amount of 5×10 -3 to 5 mols per mol of the coupler.
Claim 10
Dependent Claim 39 words
The method as claimed in claim 1, wherein the compound represented by formula (I-a) or (III-a) is added into one of the layers of the photographic material in an amount of 1×10 -2 to 1×10 -7 mol/m 2 .
Claim 11
Dependent Claim 24 words
The method as claimed in claim 1, wherein the content of chloride ions in the color developer is 4.0×10 -2 to 1.0×10 -1 mol/l.
Claim 12
Dependent Claim 24 words
The method as claimed in claim 1, wherein the content of bromide ions in the color developer is 5.0×10 -5 to 5.0×10 -4 mol/l.
Claim 13
Dependent Claim 27 words
The method as claimed in claim 1, wherein the color developer contains benzyl alcohol in an amount of 2.0 ml or below per liter of the developer.
Claim 14
Dependent Claim 15 words
The method as claimed in claim 1, wherein the color developer contains an organic preservative.

References Cited (Backward Citations)

US4770987A Cited
US4851326A Cited
US4880728A Cited
US4830955A Cited
US4853321A Cited
EP0258662A2 Cited
EP0277589A2 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1995-03-03 1995-09-02 1996-03-03 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1999-03-03 1999-09-02 2000-03-03 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2003-03-03 2003-09-02 2004-03-03 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag