GB695875A - Photographic process - Google Patents

Photographic process

Info

Publication number
GB695875A
GB695875A GB1494650A GB1494650A GB695875A GB 695875 A GB695875 A GB 695875A GB 1494650 A GB1494650 A GB 1494650A GB 1494650 A GB1494650 A GB 1494650A GB 695875 A GB695875 A GB 695875A
Authority
GB
United Kingdom
Prior art keywords
filter layer
aqueous solution
solution
pyrazolone
colour
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
Application number
GB1494650A
Inventor
Karl Otto Ganguin
Eric Macdonald
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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
Priority to BE503947D priority Critical patent/BE503947A/xx
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB1494650A priority patent/GB695875A/en
Priority to FR1044777D priority patent/FR1044777A/en
Publication of GB695875A publication Critical patent/GB695875A/en
Expired 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
    • G03C1/00Photosensitive materials
    • G03C1/76Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/825Photosensitive materials characterised by the base or auxiliary layers characterised by antireflection means or visible-light filtering means, e.g. antihalation
    • G03C1/83Organic dyestuffs therefor
    • G03C1/832Methine or polymethine dyes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)

Abstract

695,875. Colour photography. IMPERIAL CHEMICAL INDUSTRIES, Ltd. June 15, 1951 [June 15, 1950], No. 14946/50. Class Class 98 (ii). An exposed multilayer colour photographic material comprising differently colour sensitized silver halide emulsion layers, at least one filter layer containing a yellow non-diffusible styryl dye, is developed and the filter layer is subsequently decolorized by treatment with an aqueous solution of an amino compound of the formula R-NH 2 , wherein R is an alkyl, aralkyl, amino, alkylamino, aralkylamino, arylamino, aminoalkylene or hydroxy group. The styryl dye may be non-diffusible owing to its molecular structure or owing to treatment with a precipitating agent or owing to the method of forming the coating composition. The solution of the amino compound preferably also contains a surface-active agent, e.g. a condensation product of a phenol or alkylphenol with ethylene oxide, a condensation product of an aliphatic alcohol, e.g. cetyl alcohol, with ethylene oxide, an alkylated sulphonated aromatic hydrocarbon, or a quaternary ammonium salt containing a long alkyl chain, e.g. cetyltrimethylammonium bromide. The free amino compound may be formed in situ by adding alkali to a salt thereof, but a preformed free amino compound or hydrate thereof, e.g. an aqueous solution of ethylene diamine, 4- sulphophenylhydrazine or hydrazine hydrate is preferably used. The material may be subsequently treated with a dilute alkali solution. The styryl dye may be one formed by condensing a reactive methylene compound with an anil of a substituted benzaldehyde, preferably containing solubilizing groups. Numerous substituted benzaldehydes are specified, and the reactive methylene compound may be 1-#- octadecenylsuccinamido - 4 - w - cyanoacetbenzene, a thioindoxyl, 1-(4<SP>1</SP>-phenoxy-3<SP>1</SP>-sulphophenyl) - 3 - heptadecyl - 5 - pyrazolone, 3- heptadecyl- 5 - pyrazolone, or 1 - (31 - carboxyphenyl) - 3 - p - stearamidophenyl - 5 - pyrazolone. A soluble salt of the dye may be incorporated in a gelatin solution and the composition coated as a filter layer. Diffusible dyes may be precipitated, e.g. with a high molecular weight base, in the gelatin, or may be dissolved together with a water-insoluble waterpermeable resin, e.g. polyvinyl acetate in a volatile organic water-miscible solvent, and the solution dispersed in the gelatin and the solvent evaporated off. In example 1, a support is successively coated with a red-sensitive emulsion layer containing the sodium salt of 1- hydroxy - 2 - naphthoylamino - 2<SP>1</SP> - (methyloctadecylamino) - benzene - 5<SP>1</SP> - sulphonic acid, a green-sensitive emulsion layer containing the sodium salt of 1-(4<SP>1</SP>-phenoxy-3<SP>1</SP>-sulphophenyl)- 3 - heptadecyl - 5 - pyrazolone, a yellow gelatin filter layer containing the sodium salt of 1- (41 - phenoxy - 31 - sulphophenyl) - 3 - heptadecyl - 4 - p - N - methyl : N - # - sulphoethylaminobenzylidene) - 5 - pyrazolone, and a blue-sensitive emulsion layer containing the colour coupler described in example 3 of Specification 486,848. After exposure, colour development, rinsing, treating in a stop bath consisting of an aqueous solution of potassium dihydrogen phosphate, washing, removing silver, washing, fixing, and again washing, the filter layer is decolorized by treatment in an aqueous solution of hydrazine hydrate containing a condensation product of octyl cresol with about 10 molecular proportions of ethylene oxide or with an aqueous solution of ethylene diamine or with a solution obtained by adding aqueous ammonia to aqueous hydroxylamine hydrochloride. In example 2, the material and procedure are similar, but the filter layer is decolorized by treatment in an aqueous solution of sodium thiosulphate and hydrazine hydrate. In example 3, the material is similar, except that the filter layer contains as the dye the sodium salt of 1-#-octadecenylsuccinamido- 4 - w - (p - - p : #<SP>1</SP> - di - carboxyethyl) - aminobenzylidene) - # - cyanoacetobenzene, and the decolorization is effected as in example 2.
GB1494650A 1950-06-15 1950-06-15 Photographic process Expired GB695875A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
BE503947D BE503947A (en) 1950-06-15
GB1494650A GB695875A (en) 1950-06-15 1950-06-15 Photographic process
FR1044777D FR1044777A (en) 1950-06-15 1951-06-14 Photographic process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1494650A GB695875A (en) 1950-06-15 1950-06-15 Photographic process

Publications (1)

Publication Number Publication Date
GB695875A true GB695875A (en) 1953-08-19

Family

ID=10050313

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1494650A Expired GB695875A (en) 1950-06-15 1950-06-15 Photographic process

Country Status (3)

Country Link
BE (1) BE503947A (en)
FR (1) FR1044777A (en)
GB (1) GB695875A (en)

Also Published As

Publication number Publication date
FR1044777A (en) 1953-11-20
BE503947A (en)

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