US2341372A - Process for the production of photographic color images - Google Patents

Process for the production of photographic color images Download PDF

Info

Publication number
US2341372A
US2341372A US341180A US34118040A US2341372A US 2341372 A US2341372 A US 2341372A US 341180 A US341180 A US 341180A US 34118040 A US34118040 A US 34118040A US 2341372 A US2341372 A US 2341372A
Authority
US
United States
Prior art keywords
color
silver halide
production
photographic
color images
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
US341180A
Other languages
English (en)
Inventor
Frohlich Alfred
Schneider Wilhelm
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.)
GAF Chemicals Corp
Original Assignee
General Aniline and Film Corp
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 General Aniline and Film Corp filed Critical General Aniline and Film Corp
Application granted granted Critical
Publication of US2341372A publication Critical patent/US2341372A/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
    • G03C7/32Colour coupling substances
    • G03C7/327Macromolecular coupling substances

Definitions

  • This invention relates tographic color images.
  • This invention has as an object. an improved method for making photographic color images.
  • A. further object is a method for improving the manufacture of color formers fast to diffusion.
  • condensation products are feebly colored powders, easily soluble in diluted alkalies.
  • the solutions showing a pH-value of 912 may be added to the photographic emulsion at any point of the manufacturing process. If necessary, these compounds may be added previously to a gelatin solution, whereupon this gelatin may be subjected to a washing process before it has soliditied and before it is cut into small cubes, in order to dissolve out eventually uncondensed parts of the reaction components. The gelatin thus treated is then added to the photographic emulsion.
  • the silver halide emulsion thus obtained which, before casting, may be subjected to a short washing process, is worked up into photographic layers in a manner known per se, said layers being arranged on one or both sides of a support, if necessary, on top of one another and being sensitized for diflerent spectral regions.
  • the silver halide emulsions may be worked up also in a different manner. According to U. S. Patent 2,186,730, there may be arranged for instance on a support differently sensitized emulsions bearing various colorformers in the form of minute particles.
  • the manufacture of the color images can be accomplished in'various ways, for instance ac-- cording to U. S. patent application Ser. No. 111, 250, filed November 17, 1936, and U. S. Patents 2,179,228, 2,179,238, 2,186,730, 2,178,612 and 2,186,849.
  • the images may be formed in the exposed emulsion layers by simple color forming development or reversal development according to U. S. Patents 2,229,137 and 2,179,234.
  • the color formers according to this invention may be employed together with other color formers fast to difiusion within the different emulsion layers, according to U. S. Patents 2,179,- 238, 2,178,612, 2,186,849, 2,186,850, 2,179,244 and 2,186,732.
  • Example I 94 grams of phenol and 84 grams of salicylic aldehyde are heated to boiling and after adding 1 gram of gaseous hydrochloric acid, the whole is boiled under reflux for three hours. The condensation product thus obtained is dissolved in 200 cc. of glacial acetic acid and precipitated with 3 liters of ether. A feebly red powder soluble in alkalies is obtained.
  • Example I! condensation product thus obtained is diluted with 100 cc. of ether and precipitated with 1 liter of benzine. Dissolution in a small amount of ether and precipitation with benzine are repeated three times. A grey powder is then obtained, soluble in alkalies with a feebly yellow color.
  • Example III 100 grams of m-cresol and 84 grams of salicylic aldehyde are heated to boiling under reflux for 5 hours and a feeble current of gaseous HCl is slowly conducted through the reaction mixture.
  • the condensation product thus obtained is diluted with 100 cc. of ether and precipitated with 1 liter of benzine. Dissolution in a small amount of ether and precipitation with benzine are repeated three times. A grey powder is then obtained, which is soluble in alkalies with a feebly yellow color.
  • Example IV 100 grams of 1-2-3-xylenol and 84 grams of salicylic aldehyde are heated to boiling under reflux for 5 hours and a feeble current of gaseous HCl is conducted therethrough.
  • the con densation product thus obtained is diluted with 100 cc. of ether and precipitated with 1 liter of benzine. Dissolution in a small amount of ether and precipitation with benzine are repeated three times. A grey powder is then obtained which is soluble in alkalies with a feebly yellow color.
  • a silver halide emulsion for color photography containing as a color former the product obtained by the condensation of a substance selected from the class consisting of phenol and its nuclear substituted alkyl derivatives with an aromatic hydroxy aldehyde.
  • compositions as defined in claim 4 wherein the hydroxyaldehyde is an ortho-aldehyde of the benzene series.
  • the improvement which comprises developing an exposed silver halide emulsion with an aromatic primary amino developer in the presence of the condensation products of a substance selected from the class consisting of phenol and its nuclear substituted alkyl derivatives with a hydroxybenzaldehyde.

Landscapes

  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • General Physics & Mathematics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Color Printing (AREA)
US341180A 1939-06-27 1940-06-18 Process for the production of photographic color images Expired - Lifetime US2341372A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI0064965 1939-06-27

Publications (1)

Publication Number Publication Date
US2341372A true US2341372A (en) 1944-02-08

Family

ID=7196224

Family Applications (1)

Application Number Title Priority Date Filing Date
US341180A Expired - Lifetime US2341372A (en) 1939-06-27 1940-06-18 Process for the production of photographic color images

Country Status (4)

Country Link
US (1) US2341372A (enrdf_load_stackoverflow)
BE (1) BE439564A (enrdf_load_stackoverflow)
CH (1) CH232632A (enrdf_load_stackoverflow)
FR (1) FR872440A (enrdf_load_stackoverflow)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2541727A (en) * 1947-12-17 1951-02-13 Gen Analine & Film Corp Diazotypes containing aldehyde reaction products of dihydroxy aryl compounds

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2541727A (en) * 1947-12-17 1951-02-13 Gen Analine & Film Corp Diazotypes containing aldehyde reaction products of dihydroxy aryl compounds

Also Published As

Publication number Publication date
CH232632A (de) 1944-06-15
BE439564A (enrdf_load_stackoverflow)
FR872440A (fr) 1942-06-08

Similar Documents

Publication Publication Date Title
US2367531A (en) Acylaminophenol photographic couplers
US2525503A (en) Production of phenazonium dyestuff images
US2424256A (en) Color developers comprising arylsulfonhydrazides and methods of developing with same
US3002836A (en) Cyan color former for color photography
US2221793A (en) Method of producing photograph dyestuff pictures
US2342620A (en) Azo-reversal process of color photography
US2341372A (en) Process for the production of photographic color images
US2569906A (en) Light-sensitive emulsions containing color formers capable of yielding nonmigratory azine dyestuffs
US2186736A (en) Coupling compounds for color forming development
US2357395A (en) Photographic emulsion
US2331326A (en) Production of colored photographic images
US2875052A (en) Photographic material for the direct production of positive photographic images
US3056674A (en) Color formers for producing yellow dye images by color development
US2154918A (en) Coupling compounds for color forming development
US2196734A (en) Colored photographic image from hydrazine compounds
US2979405A (en) Light-sensitive photographic element containing a 1-hydroxy-2-naphthoic acid anilidecolor coupler
US2411951A (en) 4,4'-bis (pyrazolone) couplers for color photography
US2147112A (en) Antihalation layer and filter layer
US2186733A (en) Color photography
US2313138A (en) Production of color photographic images
US2186719A (en) Photographic silver halide emulsions
US2186732A (en) Silver halide emulsion for color photography
US3028237A (en) Masking of cyan images in color photography
US2366324A (en) Production of color photographic images
US2186735A (en) Silver halide emulsions for color photography