US3278303A - Process for the preparation of multicolored images by the silver dyestuff bleaching method - Google Patents

Process for the preparation of multicolored images by the silver dyestuff bleaching method Download PDF

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Publication number
US3278303A
US3278303A US240458A US24045862A US3278303A US 3278303 A US3278303 A US 3278303A US 240458 A US240458 A US 240458A US 24045862 A US24045862 A US 24045862A US 3278303 A US3278303 A US 3278303A
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Prior art keywords
bleaching
bath
catalyst
silver
dyestuff
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Expired - Lifetime
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US240458A
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English (en)
Inventor
Meyer Armin
Anderau Walter
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BASF Schweiz AG
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Ciba AG
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    • 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
    • G03C7/28Silver dye bleach processes; Materials therefor; Preparing or processing such materials

Definitions

  • this process is based on the principle that dyestuffs, especially azo dye stuffs, are destroyed by an appropriate treatment in the presence of metallic silver.
  • a treatment in a neutral to acid bath containing a complex-forming agent and a bleaching catalyst is known.
  • the bleaching of the dyestuff should take place stoichiometrically depending on the silver present, in which process tour atoms of silver are required to destroy one azo group. It should thus be assumed that in material containing sevenal silver component images the gradations of the component color images are solely dependent on the gradations of the developed silver images. However, this is not the case. The gradations of the component color images are dependent on many other factors. For example, they are dependent on the nature of the individual dyestuffs, on the layer colloid, on the thickness of the layer, on the manner in which the silver is distributed within the layer and on the composition and duration of action of the bleaching bath.
  • This invention is based on the surprising observation that in the preparation of multi-colored photographic images by the silver dyestuff bleaching process especially advantageous effects can be obtained with the use of catalysts if the exposed photographic material is treated, be-v fore bleaching, in a non-developing and non-bleaching bath to which has been added a dyestutf bleaching catalyst capable of diffusion.
  • the photographic material to be used may, for example, comprise a layer support, and three layers of a hydrophilic colloid such as gelatin, one layer being dyed cyan, one magenta and the other yellow, each of which contains a developed silver image.
  • the layers may also be in a different sequence.
  • the material may contain colored particles in the manner of the mixed grain emulsions; the support can be transparent or reflecting, and other layers such as adhesive layers, intermediate layers, filter layers and covering layers may also be present.
  • the said material can contain the usual emulsion additions such as wetting agents, optical and chemical sensitizers and, in one or more layers or intermediate layers, small amounts of bleaching catalyst.
  • the dyestuff bleaching bath consists normally of an acidic aqueous solution, for example, hydrochloric acid and at least one complex-forming agent, for example, potassium bromide or thiourea.
  • This bath can likewise contain a small amount of a bleaching catalyst.
  • the amounts of catalyst that may be present in the material and/ or in the bleaching bath must be calculated in such a manner that there is not enough to bring about complete bleaching of all dyestuffs by the image silver that is present in the time available.
  • the non-developing bath containing the bleaching catalyst can be, for example, a so-called stop bath, a hardening bath, a neutral or slightly acid fixing bath or a special bath.
  • the catalyst is added to the fixing bath or to the special bath that follows the fixing bath.
  • This special bath can consist of a neutral aqueous solution of the catalyst and a wetting agent. Since the catalyst diffuses slowly, the material can be washed with water after the bath containing the catalyst and before the bleaching bath.
  • Suitable bleaching catalysts are known; quinoxalines, phenazines, quinolines, alloxazines and cinnoline can be used as bleaching catalysts.
  • an advantageous method of carrying out the process consists in exposing and developing a light-sensitive, rnulti-layer material colored with azo dyestuffs but not containing a bleaching catalyst in the usual manner, fixing it in a bath containing a thiosulfate and a bleaching catalyst and then, after intermediate washing with water, bleaching it in a bath free from a catalyst, and finally freeing it from the remaining silver in the usual manner.
  • the catalyst acts in a very even manner in the various layers and behaves favourably in respect of diffusion, so that no over bleaching of the top layers takes place, as is the case in the usual processes.
  • the gradations of the single dyestuffs in the process of the invention are adjusted in such a manner that flat, parallel color gradation curves are obtained on exposure to white light, and steep gradation curves are obtained on exposure to the light of only one color of the spectrum.
  • Example 1 To a cellulose acetate film provided with an adhesive layer the following layers are applied one after the other:
  • a red-sensitive silver bromide emulsion in gelatine containing the cyan dyestulf of the formula (2) Agelatine intermediate layer. bath containing the catalyst was omitted and the same (3) A green-sensitive silver bromide emulsion in catalyst (2 mg. per liter of bleaching bath) was added gelatine containing the magenta dyestutf of the formula to the dyestuif bleaching bath. In this case, 7 minutes (2) NH; H038 SOIH HZN OH HO HOi S SOzH (4) A yellow filter layer containing the dyestuif of were necessary in the dyestuff bleaching bath in order the formula to just complete the bleaching.
  • the color densities were measured in transmitted light by means of a Macbeth-Ansco Desitom- (5 A blue-sensitive silver bromide emulsion in gelatine containing the dyestutf of the formula Has 0 s 0 H soul Ho s and, as precipitating agent, a mixture consisting of a eter; the gamma values correspond to the straight sections reaction product of dicyanodiamidine and formaldehyde, of the gradation curves. a small proportion of sodium forinate and sodium bisulfate.
  • the images obtained are hereinafter called red wedge, Red wedge ai 09 1 A 1 1 green Wedge, e Wedge and grey Wedge.
  • the Bluewedge Blue-m film is developed in a Metol hydroquinone developer, and then treated in an acetic acid stop bath and fixing l bath containing thiosulfate. After being washed with Results analo to ihosfi Obtalned 1n the experlmel'lt water, the film is treated for 10 minutes in a bath conwith the catalyst in the intermediate bath are obtained taining 3 mg.
  • dyestulf bleaching bath 198 parts of 1-amino-2:5-dimethoxy-4-nitrobenzene are diazotized in a suspension acidified with hydrochloric rigizi s bromlde '"I i8 acid and the diazo compound so obtained is coupled with Hydrochloric acid (36% Strength) "cc" 361 parts of 1-acetylamino-8-hydroxynaphthalene-3zo-dt- 1.25% solution of the addition product of 35 mols 6O .Sulfonic i
  • the p q dyestufi so Obtamed of ethylene oxide and 1 mol of octadecyl is reduced in an alkaline bath with sodlum sulfide to form alcohol cc" 10 the amlnomonoazo dyestuff.
  • ThlS dyestuff 1s purified by Made up with water to 1000 recrystallization, diazotized, and the diazo compound coupled with 542 parts of l-(4-benzoylamino-benzoylamino)-
  • the film is then Washed with Water, the residual silver 5 8-hydroxynaphthalene-3:6-disulfonic acid in a mixture of rehalogenated with a copper nitrate hath made strongly pyridine and aqueous ammonia.
  • the disazo dyestuif so acidic with hydrochloric acid the film washed again with obtained is freed from violet-colored impurities by rewater, fixed a second time, again washed with water and peated recrystallization.
  • the dyestulf in the green-sensitive layer is prepared by mined by experiment and is just sufficient to bleach the 70 coupling diazotized 1-amino-4-nitrobenzene-2 -sulfonic dyestuffs completely in all the layers at areas that. had acid with 2-amino-8-hydroxynaphthalene-6-sulfonic acid been highly exposed.
  • the dyestutf in the yellow filter layer is prepared as follows:
  • Example 2 The same procedure is adopted as described in Example 1, but using, after fixing and subsequent washing with Water, instead of the bath containing 2-amino-3-hydroxy phenazine hydrochloride, a bath containing 4 cc. of a 1.25% solution of the addition compound of 35 rnols of ethylene oxide and 1 mol of octadecyl alcohol per liter, and one of the following catalysts:
  • the 2-amino-3-hydroxyphenazine-x-sulfonic acid (e) can be obtained by sulfonating 2-amino-3-hydroxyphenazine with fuming sulfuric acid.
  • the azine compound of the Formula 6 is obtained when the monoazo dyestuff prepared by coupling diazotized l-aminobenzene-4-sulfonic acid and Z-phenylamino-S-hydroxynaphthalene-7-sulfonic acid in an acid medium is heated in a strongly acid medium (hydrochloric acid,
  • the azine compound of the Formula 7 may be prepared as follows: 0.1 mol of the compound of Formula 6 is dissolved in 860 cc. of 1 N-sodium hydroxide and 78 g. of 82% sodium hydrosulfite added at 70 C. in the course of 5 minutes. As soon as the reaction mixture is turned yellow-brown, concentrated hydrochloric acid is added until a strong Congo-acid reaction is obtained. The resulting precipitate is filtered off and washed free from acid with water. The gray-green residue is dissolved in a dilute solution of sodium hydroxide, and the pH value adjusted to 6.5 with acetic acid.
  • the product is then salted out with sodium acetate, filtered off, dissolved in water to purify it further, the impurities filtered off and sodium chloride added.
  • the crystalline precipitate is suction-filtered and then dried in vacuo at 40 to 50 C. A dark-brown powder is obtained. The yield is about 85% of the theoretical.
  • the step which comprises treating the exposed photographic material before the dyestuff bleaching operation in a non-developing and non-bleaching bath to which has been added a dyestuff bleaching catalyst that is capable of diffusing.
  • the step which comprises treating the exposed photographic material before the dyestutf bleaching operation in a bath for fixing the silver image which bath contains a dyestuff bleaching catalyst that is capable of diffusing.
  • the step which comprises treating the exposed photographic material before the dyestulf bleaching operation in a hardening bath which contains a dyestuif bleaching catalyst that is capable of diffusing.
  • the step which comprises treating the exposed photographic material before the dyestuff bleaching operation in a bath for fixing the silver image which bath contains as .a dyestulf bleaching catalyst an azine compound that is capable of diffusing.
  • the step which comprises treating the exposed photographic material before the dyestuif bleaching operation in a hardening bath which contains as a dyestulf bleaching catalyst an azine compound that is capable of diffusing.
  • the step which comprises treating the exposed photographic material after the treatment with the fixing bath and before the dyestufi bleaching operation in a special bath which contains as a dyestuff bleaching catalyst an azine compound that is capable of diffusing.
  • the step which comprises treating the exposed photographic material before the dyestulf bleaching operation in a bath for fixing the silver image which bath contains 2-amino-3-hydroxyphenazine as a dyestulf bleaching catalyst.
  • the step which comprises treating the exposed photographic material before the dyestutf bleaching operation in a bath for fixing the silver image which bath contains 2:3-diaminophenazine as a dyestufi" bleaching catalyst.
  • the step which comprises treating the exposed photographic material before the dyestuff bleaching operation in a bath for fixing the silver image which bath contains riboflavin as a dyestuff bleaching catalyst.
  • the step which comprises treating the exposed photographic material before the dyestuff bleaching operation in a bath for fixing the silver image which bath contains Z-methylquinoxaline as a dyestuff bleaching catalyst.
  • the step which comprises treating the exposed photographic material before the dyestuff bleaching operation in a bath for fixing the silver image which bath contains the azine compound of the formula ,as a dyestuflf bleaching catalyst.
  • the step which comprises treating the exposed photographic material before the dyestutf bleaching operation in a bath for fixing the silver image which bath contains the azine compound of the formula HOaS as a dyestufi bleaching catalyst.
  • the step which comprises treating' the exposed photographic material before the dyestuff bleaching operation in a bath for fixing the silver image which bath contains the azine compound of the formula as a dyestutf bleaching catalyst.

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
  • Coloring (AREA)
  • Catalysts (AREA)
  • Cosmetics (AREA)
US240458A 1961-12-20 1962-11-27 Process for the preparation of multicolored images by the silver dyestuff bleaching method Expired - Lifetime US3278303A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH1483761A CH405929A (de) 1961-12-20 1961-12-20 Verfahren zur Herstellung mehrfarbiger Bilder nach der Silberfarbbleichmethode

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US (1) US3278303A (US20020128544A1-20020912-P00008.png)
BE (1) BE626198A (US20020128544A1-20020912-P00008.png)
CH (1) CH405929A (US20020128544A1-20020912-P00008.png)
DE (1) DE1154345B (US20020128544A1-20020912-P00008.png)
ES (1) ES283541A1 (US20020128544A1-20020912-P00008.png)
FR (1) FR1341169A (US20020128544A1-20020912-P00008.png)
GB (1) GB969134A (US20020128544A1-20020912-P00008.png)
NL (1) NL286940A (US20020128544A1-20020912-P00008.png)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3340060A (en) * 1963-09-24 1967-09-05 Ciba Ltd Process for the production of color images by the silver dyestuff bleaching method
US3443949A (en) * 1964-10-22 1969-05-13 Ciba Ltd Dyestuff bleaching catalysts for the silver dyestuff bleaching process
US3455690A (en) * 1965-03-02 1969-07-15 Ciba Ltd Photographic material for the silver dyestuff bleaching process
US3656953A (en) * 1969-03-13 1972-04-18 Ciba Geigy Ag Silver dyestuff bleaching process using quinoxaline catalyst
US3957516A (en) * 1973-05-17 1976-05-18 Ciba-Geigy Ag Preparation for the processing of photographic materials

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1257569B (de) * 1965-04-15 1967-12-28 Agfa Gevaert Ag Verfahren zur Herstellung farbphotographischer Bilder nach dem Silberfarbbleichverfahren

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB466290A (en) * 1935-01-12 1937-05-26 Cinecolor Inc Improvements in or relating to the mordanting of photographic silver images
US2183395A (en) * 1938-12-12 1939-12-12 Gaspar Bela Light-sensitive material for producing photographic dye images
US2221793A (en) * 1938-05-17 1940-11-19 Gaspar Bela Method of producing photograph dyestuff pictures
US2304987A (en) * 1940-02-22 1942-12-15 Eastman Kodak Co Method of lowering contrast of dye images
US2322084A (en) * 1940-01-11 1943-06-15 Eastman Kodak Co Simultaneous bleaching and fixing bath
US2518710A (en) * 1948-03-27 1950-08-15 Gen Aniline & Film Corp Lumazines and alloxazines as catalysts in dye bleach baths for color photography
US2564238A (en) * 1946-12-14 1951-08-14 Gen Aniline & Film Corp Silver azo dye bleach-out process and bleaching baths for use therein
US2699394A (en) * 1950-12-15 1955-01-11 Gaspar Bela Production of photographic dye images

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB466290A (en) * 1935-01-12 1937-05-26 Cinecolor Inc Improvements in or relating to the mordanting of photographic silver images
US2221793A (en) * 1938-05-17 1940-11-19 Gaspar Bela Method of producing photograph dyestuff pictures
US2183395A (en) * 1938-12-12 1939-12-12 Gaspar Bela Light-sensitive material for producing photographic dye images
US2322084A (en) * 1940-01-11 1943-06-15 Eastman Kodak Co Simultaneous bleaching and fixing bath
US2304987A (en) * 1940-02-22 1942-12-15 Eastman Kodak Co Method of lowering contrast of dye images
US2564238A (en) * 1946-12-14 1951-08-14 Gen Aniline & Film Corp Silver azo dye bleach-out process and bleaching baths for use therein
US2518710A (en) * 1948-03-27 1950-08-15 Gen Aniline & Film Corp Lumazines and alloxazines as catalysts in dye bleach baths for color photography
US2699394A (en) * 1950-12-15 1955-01-11 Gaspar Bela Production of photographic dye images

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3340060A (en) * 1963-09-24 1967-09-05 Ciba Ltd Process for the production of color images by the silver dyestuff bleaching method
US3443949A (en) * 1964-10-22 1969-05-13 Ciba Ltd Dyestuff bleaching catalysts for the silver dyestuff bleaching process
US3455690A (en) * 1965-03-02 1969-07-15 Ciba Ltd Photographic material for the silver dyestuff bleaching process
US3656953A (en) * 1969-03-13 1972-04-18 Ciba Geigy Ag Silver dyestuff bleaching process using quinoxaline catalyst
US3957516A (en) * 1973-05-17 1976-05-18 Ciba-Geigy Ag Preparation for the processing of photographic materials

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NL286940A (US20020128544A1-20020912-P00008.png)
FR1341169A (fr) 1963-10-25
GB969134A (en) 1964-09-09
CH405929A (de) 1966-01-15
DE1154345B (de) 1963-09-12
BE626198A (US20020128544A1-20020912-P00008.png)
ES283541A1 (es) 1963-07-01

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