GB565929A - Improvements in the production of coloured photographs - Google Patents

Improvements in the production of coloured photographs

Info

Publication number
GB565929A
GB565929A GB456943A GB456943A GB565929A GB 565929 A GB565929 A GB 565929A GB 456943 A GB456943 A GB 456943A GB 456943 A GB456943 A GB 456943A GB 565929 A GB565929 A GB 565929A
Authority
GB
United Kingdom
Prior art keywords
naphthol
disulphonic acid
diacetylaminostilbene
cyanacetylcoumarone
disodium
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
GB456943A
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.)
Kodak Ltd
Original Assignee
Kodak 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 Kodak Ltd filed Critical Kodak Ltd
Priority to GB456943A priority Critical patent/GB565929A/en
Publication of GB565929A publication Critical patent/GB565929A/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
    • G03C1/815Photosensitive materials characterised by the base or auxiliary layers characterised by means for filtering or absorbing ultraviolet light, e.g. optical bleaching
    • G03C1/8155Organic compounds therefor

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Heat Sensitive Colour Forming Recording (AREA)
  • Color Printing (AREA)

Abstract

A colour photograph comprises a layer containing a dye image and unused colour coupler employed for forming the dye image and inseparably superimposed on such layer, an outermost non-sensitive layer which transmits not more than 30 per cent, preferably not more than 15 per cent, at and below 350 mm , and not less than 70 per cent at and above 450mm . The light-fastness of the image dye is improved and deterioration due to decomposition of the coupler prevented. The ultra-violet absorbing layer is preferably coated over the colour photograph after the dye image has been formed. The coupler may be contained in fine discrete particles as described in Specifications 524,154, 524,554, 524,555 and 541,589, [all in Group XX]. Ultra-violet absorbing substances specified are 3 : 31-dialkyloxacyanine halides, diacylaminostilbene derivatives (e.g. the disodium and the bis-dioctylamine salts of 4 : 41-diacetylaminostilbene - 2 : 21 - disulphonic acid and disodium 4 : 41-di-(m-aminobenzoyl)-aminostilbene-2 : 21-disulphonate), 1 : 11-dihydroxy - 6 : 61-dinaphthylamine 3 : 31-disulphonic acid, aesculin, p - hydroxybenzaldehyde, 3 - methoxy - 4 - hydroxybenzaldehyde, 2 : 4 - dihydroxybenzaldehyde, quinine, primuline, di-4-(p-aminobenzoyl)-aminodiphenylurea-2 : 21-disulphonic acid and disalicylbenzidide. The ultra-violet absorbing coating (a) prepared from an aqueous solution of gelatin and disodium 4 : 41-diacetylaminostilbene-2 : 21-disulphonate; (b) from a composition obtained by dispersing a sodium hydroxide-ethyl alcohol solution of disalicylbenzidide in gelatin and neutralizing with citric acid; (c) from an ethyl alcohol solution of polyvinyl acetate containing the bis-dioctylamine salt of 4 : 41-diacetylaminostilbene 2 : 2-disulphonic acid; or (d) from an ethyl alcohol solution of ethyl cellulose containing n-butyl propionate and the bis-dioctylamine salt of 4 : 41 - diacetylaminostilbene - 2 : 21-disulphonic acid. In an example, exposed, colour developed, fixed, washed and dried material comprising a support coated with a light-sensitive layer made according to example (2) of Specification 541,589, [Group XX], (except that the emulsion is red-sensitive) and a light-sensitive layer made according to example (4) of Specification 541,589, [Group XX], (except that the emulsion is green - sensitive and the coupler is 2-cyanacetylcoumarone - 5 - sulphon - N - (n-amyltert-amylsulphanilide) is coated with one of the coatings specified. Other couplers specified are 5-diamylnaphthalenesulphonamido-1-naphthol, 5 - [N - (p - toluenesulphonyl)] - (N1 - b - hydroxy - ethyl) - amino - 1 - naphthol, 5-diphenylethersulphonamido-1-naphthol, 5-phenoxyacetamino-1-naphthol, 5 - (N - benzoyl - N - b - hydroxyethyl) - amino - 1 - naphthol, 5 - amyldiphenylethersul - phonamido - 1 - naphthol, 2 : 4 - dichloro - 4 - (p - nitrobenzoyl-b -hydroxyethylamino) - 1 - naphthol, 5-(p-amylphenoxybenzenesulphonamido)-1-naphthol, 5-(N-benzyl-N-n-valerylamino)-1-naphthol, 5-caproylamino - 1 - naphthol, 2-chloro-5-(N - n - valeryl: N - p - isopropylbenzylamino) - 1 - naphthol, 2 : 4 - dichloro - 5 - palmitylamino - 1 - naphthol, 5-b -phenylpropionylamino-1-naphthol, and monochlor-5-(N-g -phenylpropyl-n-p-sec-amylbenzoylamino) -1-naphthol for cyan and 2-cyanacetylcoumarone-5-sulphon-N-methylanilide, 2 - cyanacetylcourmarone - 5 - sulphon - dimethylamide, 2-cyanacetyl-5-benzoylaminocoumarone, 2-cyanacetyl-5-(p-sec-amylbenzoylamino)-coumarone, 2-cyanacetylcoumarone-N-n-amyl: p-sec-amylsulphanilide, 2-cyanacetylcoumarone - 5 - sulphon - N - n - butylanilide, and 2-cyanacetylcoumarone-5-(N-g -phenylpropyl)-p-tert amylsulphonanilide for magenta. Disodium - 4 : 41 - diacetylaminostilbene - 2 : 21-disulphonate is prepared by dissolving 4 : 41-diaminostilbene - 2 : 21 - disulphonic acid in aqueous sodium carbonate solution reacting with acetic anhydride, adding further sodium carbonate solution and recrystallising the precipitate. The bis-dioctylamine salt is prepared by adding to an aqueous solution of the disodium salt a solution of dioctylamine in glacial acetic acid, ethyl alcohol, and water. 1 : 11-Dihydroxy-6 : 61-dinaphthylamine-3 : 31-disulphonic acid is prepared by adding aqueous sodium bisulphite to a caustic soda solution of J-acid. Specifications 493,308, 501,190, 524,320, 524,377, 524,379 and 555,508, [Group XX], also are referred to.
GB456943A 1943-03-20 1943-03-20 Improvements in the production of coloured photographs Expired GB565929A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB456943A GB565929A (en) 1943-03-20 1943-03-20 Improvements in the production of coloured photographs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB456943A GB565929A (en) 1943-03-20 1943-03-20 Improvements in the production of coloured photographs

Publications (1)

Publication Number Publication Date
GB565929A true GB565929A (en) 1944-12-05

Family

ID=9779617

Family Applications (1)

Application Number Title Priority Date Filing Date
GB456943A Expired GB565929A (en) 1943-03-20 1943-03-20 Improvements in the production of coloured photographs

Country Status (1)

Country Link
GB (1) GB565929A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2632701A (en) * 1949-05-04 1953-03-24 Eastman Kodak Co Ultraviolet filter on photographic layers
US2747996A (en) * 1952-10-31 1956-05-29 Eastman Kodak Co Photographic element protected against action of ultraviolet radiation
DE1135756B (en) * 1959-01-14 1962-08-30 Polaroid Corp Process for the production of colored transfer images protected against the harmful effects of ultraviolet light
DE1155673B (en) * 1959-01-14 1963-10-10 Polaroid Corp Process for the production of color photographic images with improved resistance to ultraviolet light

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2632701A (en) * 1949-05-04 1953-03-24 Eastman Kodak Co Ultraviolet filter on photographic layers
US2747996A (en) * 1952-10-31 1956-05-29 Eastman Kodak Co Photographic element protected against action of ultraviolet radiation
DE1135756B (en) * 1959-01-14 1962-08-30 Polaroid Corp Process for the production of colored transfer images protected against the harmful effects of ultraviolet light
DE1155673B (en) * 1959-01-14 1963-10-10 Polaroid Corp Process for the production of color photographic images with improved resistance to ultraviolet light

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