US2923627A - Colour photography - Google Patents

Colour photography Download PDF

Info

Publication number
US2923627A
US2923627A US724931A US72493158A US2923627A US 2923627 A US2923627 A US 2923627A US 724931 A US724931 A US 724931A US 72493158 A US72493158 A US 72493158A US 2923627 A US2923627 A US 2923627A
Authority
US
United States
Prior art keywords
developing
colour
dye
hydroxylamine
photographic
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.)
Expired - Lifetime
Application number
US724931A
Other languages
English (en)
Inventor
Mason Leslie Frederick Alfred
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ilford Imaging UK Ltd
Original Assignee
Ilford Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Ilford Ltd filed Critical Ilford Ltd
Application granted granted Critical
Publication of US2923627A publication Critical patent/US2923627A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C7/00Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/30Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
    • G03C7/407Development processes or agents therefor
    • G03C7/413Developers

Definitions

  • This invention relates to colour photography and more particularly to developing compositions for use in colour photographic processes.
  • a colour image is formed by developing a silver salt image in a photographic element by means of a developing solution which contains an aromatic primary amino developing agent and a dye intermediate (hereinafter referred to as a colour coupler) such that the oxidation products of the developing agent formed during its developing action couple with the colour coupler to constitute a dye in situ with the developed silver image, the dye commonly being anazomethine or quinone-imine dye.
  • a developing solution which contains an aromatic primary amino developing agent and a dye intermediate (hereinafter referred to as a colour coupler) such that the oxidation products of the developing agent formed during its developing action couple with the colour coupler to constitute a dye in situ with the developed silver image, the dye commonly being anazomethine or quinone-imine dye.
  • the developing agents used in this type of process are usually derivatives of p-phenylene diamine, well-known examples being N.N-diethyl p-phenylene diamine and 2- nited States Patent amino-S-diethyl amino toluene and their salts and sulphur dioxide reaction products.
  • These agents unfortunately have a tendency to oxidise in the air and, since the oxidation products will combine with the colour coupler present, the solutions in use acquire, more or less rapidly, a scum consisting mainly of the dye thus formed. This is so serious a difficulty that such developers must frequently be discarded long before they have outlived their useful activity.
  • the extent of scum formation depends on the extent of aerial oxidation which occurs, and this in turn is found to be greatest at higher pH values. Accordingly, a balance must be struck between the activity of the developer, which is reduced by lowering the pH of the solution, and the liability of the developer to oxidation, which is increased by increasing the pH of the solution, i.e. some sacrifice of developer activity must be made in order to aviod undue oxidation. Generally, the pH of the solutions is adjusted to about 10.5.
  • a photographic developing composition for use in colour developing a developable sliver salt image in a photographic element may comprise an aromatic primary amino developing agent, a colour coupler which is capable of combining with the oxidation products of such developer to form a dye, and hydroxylamine or .a salt thereof, the said. composition on dissolution in water having a pH of .at least 11.25.
  • aryl group -R may be a phenyl'or naphthyl group or a corresponding group containing, for example, alkyl, aralkyl, aryl, sulphonic acid or halogen substituents. Specific compounds of value are: 1'
  • a photographic developing composition for use in colour developing a developable silver salt image in a photographic element comprises an aqueous alkaline solution of an aromatic. primary amino developing agent, a colour coupler which is capable of combining with the oxidation products of such developer to form a dye, hydroxylamine or, a 'salt thereof and ascorbic acid and/ or a tetronic compound of the formula above set forth.
  • the invention further includes processes of colour development employing such solutions.
  • hydroxylamine and ascorbic acid or tetronic compound are not unduly critical. Generally a quantity of the orderof 0.5 to 1.5 g./litre of hydroxylfective in reducing, or even eliminating, dye scum. It
  • agents. are N.N.-diethyl p-plienylene diamine or '2-a'mino- 5'-diethyl amino .toluene, or:theirsalts. or sulphur dioxide Patented Feb. 2, 1960 reaction products.
  • a suitable alkalinity in the developing composition is conveniently achieved by the use of alkali carbonates or, where a high pH is desired, mixtures of tribasic sodium phosphate and dibasic sodium phosphate, these latter compounds being particularly useful owing to their good buffering properties.
  • thedeveloping compositions of the invention may include other ingredients common to photographic developers, e.g. alkali, ammonium or amine sulphites and alkali or ammonium bromides. it is also frequently of advantage to include a proportion of ethyl alcohol in the developer.
  • the invention accordingly further includes in solid form or in strong aqueous solution a composition of aromatic primary amino developing agent, hydroxylamine and ascorbic acid and/or tetronic compound as defined.
  • photographic element which comprises anaqueous alkaline solution of an aromatic primary amino developing agent, a colour coupler which is capable of combining with the oxidation products of such developer to form a dye, a. compound selected fromthe class consisting of hydroxylamine and its salts in a concentration of 0.5 to 1.5 g./litre and a compound selected from the class consisting of ascorbic acid and tetronic compounds of the formula:
  • the pH of the developer was in all cases approximately 10.50. It will be seen that while hydroxylamine alone is ineifective at this pH, and both ascorbic acid and a typical tetronic compound afiord only limited protection against scum formation, the combination of the two (developers D, E, F, G and H) shows a very much enhanced protective eflect.
  • a photographic developing composition for use in colour developing a developable silver salt image in a photographic element which comprises an aqueous alkaline solution of an aromatic primary amino developing agent, a colour coupler which is capable of combining with the oxidation products of such developer to form a dye, a compound selected from the class consisting of hydroxylamine and its salts and a compound selected from the class consisting of ascorbic acid and tetronic compounds of the formula:
  • R is selected from the class consisting of phenyl and naphthyl groups, and phenyl and. naphthyl groups containing alkyl, aralkyl, aryl, sulphonic acid and halogen substituents, and X is selected from the class consisting of the oxygen atom and the imino group.
  • a photographic developing composition for use in colour developing a developable silver salt image in a photographic element which comprises an aqueous solution of pH 9 to 11.25 of an aromatic primary amino developing agent, a colour coupler which is capable of combining with the oxidation products of such developing agent to form a dye, hydroxylamine in a concentration of 0.5 to 1.5 g./litre, and 4-phenyl-2 oxytetronimide in a concentration of 0.1 to 0.5 g./litre.
  • a photographic developing composition for use in colour developing a developable silver salt image in a photographic element which comprises an aqueous solution of pH 9 to 11.25 of an aromatic primary amino developing agent, a colour coupler which is capable of combining with the oxidation products of such developing agent to form a dye, hydroxylamine in a concentration of 0.5 to 1.5 g./litre, and 4-phenyl-2-oxytetronic acid in a concentration of 0.1 to 0.5 g./ litre.
  • a photographic developing composition for use in colour developing a developable silver salt image in a photographic element which comprises an aqueous solution of pH 9 to 11.25 of an aromatic primary amino developing agent, a colour coupler which is capable of combining with the oxidation products of such developing agent'to form a dye, alkali carbonate, hydroxylamine in a concentration of 0.5 to 1.5 g./litre, and ascorbicacid in a concentration of 0.1 to 0.5 g./ litre.
  • a photographicdeveloping. composition for use-in colour developing a developable silver salt image in a photographic element which comprises an aqueous solution of pH 9 to 11.25 of an aromatic primary amino developing agent, a colour coupler which is capable of combining with the oxidation products of such developing agent to form a dye, alkali carbonate, hydroxylamine in a concentration of 0.5 to 1.5 g./litre, and 4-phenyl-2- oxytetronimide in a concentration of 0.1 to 0.5 g./litre.
  • a photographic developing composition for use in colour developing a developable silver salt image in a photographic element which comprises an aqueous solution of pH 9 to 11.25 of an aromatic primary amino developing agent, a colour coupler which is capable of combining with the oxidation products of such developing agent to form a dye, alkali carbonate, hydroxylamine in a concentration of 0.5 to 1.5 g./1itre, and 4-phenyl-2- oxytetronic acid in a concentration of 0.1 to 0.5 g./litre.
  • a photographic developing composition for use in colour developing a developable silver salt image in a photographic element which comprises an aqueous solution of pH 9 to 11.25 of an aromatic primary amino developing agent, a colour coupler which is capable of combining with the oxidation products of such developing agent to form a dye, tribasic sodium phosphate, dibasic sodium phosphate, hydroxylamine in a concentration of concentration of 0.1 to 0.5 g./litre.
  • a photographic developing composition for use in colour developing a developable silver salt image in a photographic element which comprises an aqueous solution of pH 9 to 11.25 of an aromatic primary amino developing agent, a colour coupler which is capable of combining with the oxidation products of such developing 0.5 to 1.5 g./litre, and ascorbic acid in a concentration of 0.1 to 0.5 g./litre.
  • a photographic developing composition for use in colour developing a developable silver salt image in a agent to form a dye tribasic sodium phosphate, dibasic sodium phosphate, hydroxylamine in a concentration of 0.5 to 1.5 g./litre, and 4-pheny1-2-oxytetronic acid in a concentration of 0.1 to 0.5 g./1itre.

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
US724931A 1957-04-17 1958-03-31 Colour photography Expired - Lifetime US2923627A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB12581/57A GB830625A (en) 1957-04-17 1957-04-17 Improvements in or relating to colour photography

Publications (1)

Publication Number Publication Date
US2923627A true US2923627A (en) 1960-02-02

Family

ID=10007269

Family Applications (1)

Application Number Title Priority Date Filing Date
US724931A Expired - Lifetime US2923627A (en) 1957-04-17 1958-03-31 Colour photography

Country Status (5)

Country Link
US (1) US2923627A (enrdf_load_stackoverflow)
DE (1) DE1057875B (enrdf_load_stackoverflow)
FR (1) FR1205498A (enrdf_load_stackoverflow)
GB (1) GB830625A (enrdf_load_stackoverflow)
NL (1) NL226676A (enrdf_load_stackoverflow)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3489566A (en) * 1966-02-01 1970-01-13 Eastman Kodak Co Magneta color developer solutions

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2286662A (en) * 1938-09-02 1942-06-16 Gen Aniline & Film Corp Color photography
US2401713A (en) * 1941-07-31 1946-06-04 Eastman Kodak Co Color photography
US2656272A (en) * 1950-11-30 1953-10-20 Gen Aniline & Film Corp Stabilized azine photographic developers containing sodium metaborate as the sole alkali
GB751304A (en) * 1953-09-04 1956-06-27 Polaroid Corp Improvements in photographic processing compositions and in photographic silver image transfer processes

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB782304A (en) * 1955-06-20 1957-09-04 Ilford Ltd Improvements in or relating to the stabilisation of photographic developers

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2286662A (en) * 1938-09-02 1942-06-16 Gen Aniline & Film Corp Color photography
US2401713A (en) * 1941-07-31 1946-06-04 Eastman Kodak Co Color photography
US2656272A (en) * 1950-11-30 1953-10-20 Gen Aniline & Film Corp Stabilized azine photographic developers containing sodium metaborate as the sole alkali
GB751304A (en) * 1953-09-04 1956-06-27 Polaroid Corp Improvements in photographic processing compositions and in photographic silver image transfer processes

Also Published As

Publication number Publication date
FR1205498A (fr) 1960-02-03
NL226676A (enrdf_load_stackoverflow)
DE1057875B (de) 1959-05-21
GB830625A (en) 1960-03-16

Similar Documents

Publication Publication Date Title
US3520690A (en) Process for controlling dye gradation in color photographic element
EP0039752B1 (en) Photographic color developer solutions
US4015990A (en) Color photographic lightsensitive material
US2902367A (en) Photographic developer antioxidant
US4155764A (en) Photographic color developer composition
US2384592A (en) Single-powder photographic developers
US2923627A (en) Colour photography
GB924320A (en) Gelatin compositions for coating
US3615503A (en) Color-developing composition containing an antioxidant
US2618558A (en) Photographic developers comprising an n,n - dialkyl-p-phenylenediamine and a benzenesulfonate
GB1313469A (en) Bis-triazinylamino-stilbene derivatives
US2845349A (en) Photographic developers
US1925557A (en) Photographic developer with alkali substitute
GB687311A (en) Regeneration of exhausted photographic silver bleaching solutions
US3256092A (en) Corrosion inhibitors in bleach solutions
GB1251558A (enrdf_load_stackoverflow)
US2515147A (en) Photographic developer containing an aralkylamine and process of development
US2384593A (en) Antifoggant
US3809563A (en) Method for processing light-sensitive silver halide color photographic materials
US2311428A (en) Photographic developer
US3801322A (en) Improved process for preventing the discoloration of a color image and improving image stability
GB1495504A (en) Photographic colour developer compositions
US3178284A (en) Photographic developer compositions
US2649376A (en) Single powder developers containing stabilized alkali hydroxides
US3615534A (en) Photographic silver halide light-sensitive elements useful in preventing yellow fog