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US3099559A - Silver-free color reproduction process and composition therefor - Google Patents

Silver-free color reproduction process and composition therefor Download PDF

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US3099559A
US3099559A US836883A US83688359A US3099559A US 3099559 A US3099559 A US 3099559A US 836883 A US836883 A US 836883A US 83688359 A US83688359 A US 83688359A US 3099559 A US3099559 A US 3099559A
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color
gelatin
compound
coating
radical
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Robert F Coles
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GAF Chemicals Corp
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General Aniline and Film Corp
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    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/09—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers
    • G03F7/105—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers having substances, e.g. indicators, for forming visible images

Definitions

  • This invention relates to color photography. More particularly, this invent-ion'relates to a color process involving the production of hardened, colored gelatin relief images.
  • gelatin can be hardened by prolonged exposure to various types of radiations such as ultraviolet light or visible radiation. It is likewise known that the hardening of gelatin by radiation may be accelenated by incorporating in the gelatin certain inorganic compounds such as dichromates, i.e., sodium or potassium dichromate, metallic silver and the like. If the aforesaid radiation constitutes an optical image such as would be obtained by superimposing a pattern between the radiation source and the gelatin layer, then hardening is proportional to the intensity of the exposing radiation with the result that a hardened gelatin image is obtained. The unexposed and, therefore, unhardened gelatin portions can be removed, such as by washing, thereby leaving a hardened gelatin relief image. The image can be colored or used for the production of planographic prints.
  • radiations such as ultraviolet light or visible radiation.
  • a colored image is formed by developing a reducible silver salt image in the presence of a compound which couples during the development with the oxidation product of the developing agent and forms a dyestufi which deposits on the developed silver grains. After the metallic silver image is removed, a dyed gelatin image color forming component as the photographic element.
  • I produce a colored photographic image of hardened gelatin by irradiating gelatin in the presence of certain color couplers or color forming components characterized by the presence of a salt forming group followed by dyeing of the
  • the resulting photographic element comprising a base and light sensitive layer thereon of gelatin and color former is then exposed through a pattern to the radiations emanating from an ultraviolet lamp.
  • the so exposed coating is then immersed in a p-N,N-dialkylaminoaniline type color developer solution for a few minutes and then contacted with a solution of an oxidizing agent such as potassium ferrocyanide.
  • an oxidizing agent such as potassium ferrocyanide
  • the exposure may be carried out using visible light in which case the time of exposure required to effect hardening is somewhat longer.
  • oxidizing agents of a type commonly employed in the photographic art can be used in lieu of the potassium ferrocyanide and in this connection mention is made of such materials as ammonium and alkali metal persulfates, organic peroxides, metal perchlorates and the like. In fact, it has been my experience that any type of oxidizing agent can be used for the purpose of practicing the invention provided it does not have a destructive action on the hardened gelatinor the dye used in forming the colored image.
  • Color development of the hardened gelatin image can be achieved by means other than by the coupling reaction between the oxidation products of p-phenylenediamine color developers and the color coupling component.
  • a color developer in place of a color developer, there'may be substituted diazonium salts, aldehydes, sulfo hydrazides and the like, all of which react with the color coupler to produce a colored dye.
  • these compounds unlike the p-phenylenediamine color developers, do not require the presence of an oxidizing agent since they react directly with the color forming component.
  • R is halogen, i.e., bromine, chlorine, iodine or the like, nitro, sulfo, or an arsonic acid radical
  • R is hydrogen, alkyl or a mononuclear carbocyclic aromatic radical such as phenyl, nitrophenyl, aminophenyl, stearoylaminophenyl, octadecanesulfoamidophenyl, chlo rophenyl, tolyl, anisyl and the like
  • R is hydrogen, --COOH or -CONHR and R is a sulfonated aliphatic radical containing at least 10 carbon atoms or a sulfonated aromatic radical substituted by an aliphatic radical containing at least 10 carbon atoms.
  • R is a hydroxy aromatic radical, the hydroxy group being directly linked to a nuclear carbon atom, such as, hydroxy naphthyl, hydroxy phenyl and the like and such. radicals substituted by halogen, i.e., chlorine, bromine and the like, sulfo carboxy, lower alkyl, i.e., alkyl containing up to five carbon atoms, such as, methyl, ethyl, propyl, butyl and amyl, and lower alkoxy, the alkyl radical of which is as above, R is a long aliphatic chain containing at least ten carbon atoms, such as,
  • R has the value given above, R is zlmldazoleJ'sulfomq hydrogen or aliphatic acyl, e.g., acetyl, propionyl, bu- 5 tyryl, valeryl, capronyl, heptanoyl, caproyl, pelargonyl, i 0H undecylyl, lauroyl, myristoyl, steamy], etc., R represents a J-acid radical and A represents an arene radical, i.e., C p-phenylene, 1,4-naphthalene, etc. Hso Examples of compounds of the type embraced by 10 N Formula I are the following:
  • COMPOUND l COMPOUND 7 I 6-Slear0ylamino-2-(2-Phenyl-6-Br0mo-8-Hydroxy- 1 0 d l 2-(2'-(1 '-Hydroxy-4'-Chloro)Naphthyl) cinchoninoyl)Aminot0luene-4-Sulfonic Acid Benzimidazole 5 sulfonic Acid CH 9 r i h---N N-c-cm N OH (I H80 'smH V N i COMPOUND 2 COMPOUND 8 Z-Phenyl-6-Chl0ro-8-Hydr0cinchoninoyloctadecyli marine Benzimidazole-S-Sulfonic Acid 0 CIHASOQI C-N--C15Ha1 (IHEHW N 0H 01 Q C N use I N/ OH COMPOUND 3 S0111 6-Dec0x
  • COMPOUND 12 l-Lauryl- 2-(2'-(1'-Hydroxy)Naphthyl)BenzimidazoIe-S-Sulfonic Acid 111 on v . ⁇ C noas- N/ COMPOUND 13 1-Octadecyl-2-(2'-(1 '-Hydroxy-6'-Meth0xy )Phenyl) Benzimidazole-S-Sulfonic Acid COMPOUND 14 1 -0leyl-2- (2- (1 -Hydroxy)NaphthyDBenzimidazole-S-Carboxylic Acid I on: Q U ⁇ C 11000 N/ Examples of compounds of the type included within the ambit of Formula III are the following:
  • Couplers of the type embraced by formula III can be pre pared by conventional methods known to the art. These compounds can be synthesized by reacting a 4'- carboxyaryl-I-acid with an o-phenylenediamine of the following formula:
  • p-phenylenediamine color developers the oxidation products of which are used to couple with the couplers as set forth herein, are so well known in the photographic art that it is considered unnecessary to describe these materials in detail.
  • azine developing agents can also be used for practicing my invention.
  • the azinc developing agents are aromatic triamines which on color development with appropriate couplers give rise to phenazonium dyestutf images.
  • Such color developers are also well known in the art and in this connection reference is made to the following U.S. patents: 2,486,440, 2,522,802, 2,569,906, 2,570,116, 2,537,460.
  • an oxidizing agent in which case the p-phenylenediamine or azine developing agents can be replaced by an aromatic diazonium compound in order to form a colored image by coupling with a color forming component in order to produce the colored, hardened gelatin images.
  • aromatic diazonium com-pounds usually employed in the form of their stable diazonium sulfates, chlorobenzene sulfonates, chlorfluorides, etc., are known chemical compounds. In general, such diazonium compounds are prepared by diazotization of aromatic amines by the well known procolor aspects of the subject.
  • the method of producing hardened gelatin images as described herein is compatible with ancillary gelatin hardening agents and I have, in fact, ascertained that my hardening process can be augmented by such well known gelatin hardeners as the alkali metal dichromates, silver, silver salts and the like.
  • My method of forming colored, hardened gelatin images is eminently suitable for reproducing the colored aspects of a subject.
  • a light sensitive photographic element prepared in accordance with the present invention, is exposed to one of the primary colored aspects of a subject as represented for instance by a color separation negative or positive.
  • the resulting exposed and hardened gelatin image is then subtractively dyed and developed in accordance with the methods set forth above.
  • prepared photographic elements are then exposed to the remaining color aspects of the subject and dyed with the appropriate subtractive dye.
  • the resulting subtractively dyed color aspects are then placed in register which is then viewed through a white light source in order to reconstruct the complete color aspects of the subject.
  • a single photographic element can be used to record the In this method, a photographic element is prepared by the previous method and exposed and the image of hardened gelatin subtractively dyed to one of the color aspects of the subject. After removal of the unhardened gelatin in the non-irradiated areas, the same photographic element is given a second coating, exposed, subtractively dyed in order to record a second primary color aspect of the subject. The process of coating, exposing and dyeing is then repeated until all of the remaining color aspects of the subject have been reproduced. In this manner, all of the colors of the subject are thus recorded on a single layer.
  • This method has the advantage that once the color aspects are recorded, the problem of keeping three physically sep arate reproductions in register is eliminated.
  • My colored, hardened photographic images can be formed on a wide variety of surfaces including transparent, translucent and opaque supports such as ceramic ware, paper, glass, plastic, etc.
  • EXAMPLE I 1 gram of the compound CnHn was dissolved in 100 ml. of 3% gelatin and coated on a white opaque support to yield a coating of approximately 2-6 M. The coating thus obtained was exposed through a pattern such as a silver negative to ultraviolet radiation emanating from the lamp in a White Print Machine at slow speed (4 passes). The resulting exposed coating was then treated in the following manner:
  • a section of the coating was immersed in a p-N,N- dialkylaminoaniline type colordeveloper solution for 1-2 minutes. This was followed by immersing the coating in a potassium ferricyanide oxidizing bath for several minutes. As a result of this treatment. an indiscriminant color coupling occurred throughout the film.
  • the coating was then bathed in warm water (40-50 C.). The unhardened gelatin plus dye in the unexposed areas was thus removed by washing and a positive blue-green dye plus gelatin image remained in the areas exposed to radiation.
  • the color developer formulation used above had the following composition:
  • Example II A coating was made the manner described in Example I with the exception that instead of the hardening compound used therein a hardening compound having the formula 1sHa1 it E so H 3 was used. The film was exposed as in Example I and the exposed coating was treated in the following manner:
  • a section of the exposed coating was immersed in a color developing solution containing a 6-phenylamino-4- dimethylaminometanilic acid type as a color developer.
  • the coating was then processed in a ferricyanide oxidizing bath as before to yield an overall blue-green azine dye.
  • the processed strip was then washed as in Example I to yield a positive hardened gelatin plus blue-green azine dye in the exposed areas of the film.
  • Example IIB A section of the exposed film was bathed in diamtized sulfanilic acid and treated as in Example IB to yield a reddish magenta azo positive dye image.
  • the developer formulation used above was the same as given in Example I of U.S.P. 2,522,802 except that an equivalent amount of 6-phenylamino-4-dimethylaminometanilic acid was used in place of the developing agent of the example of the patent.
  • Example III A coating was prepared as in Example I using the hardening compound instead of the hardening compound of Example I. The material was then treated as in Example IIA. A magenta azine dye image was produced.
  • EXAMPLE iv 9 s' the greatest hardening in the gelatin next to the base which promotes better adhesion of the hardened gelatin to the base.
  • EXAMPLE v A coating of 0.5 g. of 3-(1-hydroxy-2-naphthoyl) N'-octadecylamidoisophthalic acid and 0.5 g. of sodium dichromate in 100 ml. of 3% gelatin was coated on transparent film base. The material was exposed through the base and developed as in Example I. In this case, a bluish-green dye image is obtained with p-phenylenediamine type developer and an orange with-diazotized sulfanilic acid.
  • a radiation sensitive photographic element comprising a base and a radiation sensitive coating thereon, said coating being free of silver halide and consisting essentially of gelatin and a color coupler selected from those represented by the following general formulae:
  • R is a member selected form the class consisting of halogen, nitro, sulfo and arsonic acid radicals, R is a member selected from the class consisting of hydrogen,
  • R is a member selected from the class consisting of H, COOH and CONH-R and R, is a member selected from the class consisting of sulfonated aliphatic radicals containing at least 10 carbon atoms and sulfonated aromatic radicals substituted by an aliphatic radical containing at least 10 carbon atoms;
  • R; is a water solubilizing group, R is an hydroxy aromatic radical, the hydroxy group being nuclearly attached and said radical being linked to the benzimidazole radical in the ortho position to said hydroxy group, R is a long aliphatic chain capable of rendering said compound fast to diffusion in a photographic colloid,
  • R is a member selected from the class consisting of hydrogen and aliphatic acyl radicals, R7 represents a I-acid radical and A- is an arylene group selected from the class consisting of a p-phenylene radical and a naphthylene radical.
  • a method of producing a hardened gelatin colored photographic reproduction which comprises exposing to an optical image a radiation sensitive photographic element comprising a base and a radiation sensitive coating thereon, said coating consisting essentially of gelatin and a color coupler selected from those represented by the following general formulae:
  • R is a member selected from the class consisting of halogen, nitro, sulfo and arsonic acid radicals
  • R is a member selected from the class consisting of hydrogen, alkyl and a mononuclear carbocyclic aromatic radical
  • R is a member selected from the class consisting of H, COOH and CONHR
  • R is a member selected from the class consisting of sulfonated aliphatic radicals containing at least 10 carbon atoms and sulfonated aromatic radicals substituted by an aliphatic radical containing at least 10 carbon atoms
  • R is a water solubilizing group
  • R is a hydroxy aromatic radical, the hydroxy group being nuclearly attached and said radical being linked to the benzimidazole radical in the ortho position to said hydroxy group
  • R is a long aliphatic chain capable of rendering said compound fast to diffusion in a photographic colloid
  • R is a member selected from the class consisting of hydrogen and aliphatic acyl radicals,

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Description

hardened gelatin in the exposed areas.
United States Patent eral Aniline & Film Corporation, New York, N.Y., a
corporation of Delaware No Drawing. Filed Aug. 31, 1959, Ser. No. 836,883 16 Claims. (CI. 96-48) This invention relates to color photography. More particularly, this invent-ion'relates to a color process involving the production of hardened, colored gelatin relief images.
It is known that gelatin can be hardened by prolonged exposure to various types of radiations such as ultraviolet light or visible radiation. It is likewise known that the hardening of gelatin by radiation may be accelenated by incorporating in the gelatin certain inorganic compounds such as dichromates, i.e., sodium or potassium dichromate, metallic silver and the like. If the aforesaid radiation constitutes an optical image such as would be obtained by superimposing a pattern between the radiation source and the gelatin layer, then hardening is proportional to the intensity of the exposing radiation with the result that a hardened gelatin image is obtained. The unexposed and, therefore, unhardened gelatin portions can be removed, such as by washing, thereby leaving a hardened gelatin relief image. The image can be colored or used for the production of planographic prints.
An important application of the hardening of gelatin is in the field of color photography wherein colored images of hardened gelatin are placed in register in order to reproduce the color aspectsvof a subject. In this process, a colored image is formed by developing a reducible silver salt image in the presence of a compound which couples during the development with the oxidation product of the developing agent and forms a dyestufi which deposits on the developed silver grains. After the metallic silver image is removed, a dyed gelatin image color forming component as the photographic element.
Drawbacks of such photographic elements are the need for expensive light sensitive silver halide emulsion and complex manufacturing facilities and equipment.
It has now been discovered that colored photographic dye images of hardened gelatin can be produced without recourse to expensive light sensitive silver halide emulsions and the provision of such dye images constitute the objects and purposes of this invention.
In accordance with the present invention, I produce a colored photographic image of hardened gelatin by irradiating gelatin in the presence of certain color couplers or color forming components characterized by the presence of a salt forming group followed by dyeing of the In practicing the invention, I prefer to coat, on a suitable base or support, a mixture of aqueous gelatin and color coupler.
The resulting photographic element comprising a base and light sensitive layer thereon of gelatin and color former is then exposed through a pattern to the radiations emanating from an ultraviolet lamp. The so exposed coating .is then immersed in a p-N,N-dialkylaminoaniline type color developer solution for a few minutes and then contacted with a solution of an oxidizing agent such as potassium ferrocyanide. As a result of the aforesaid treatment, indiscriminate color coupling occurs throughout the film. The coating is then developed by washing 5 ice in warm water which treatment removes the unhardened gelatin plus dye in the unexposed .areas leaving a dyed, hardened gelatin image corresponding to the areas exposed to radiation.
If desired, the exposure may be carried out using visible light in which case the time of exposure required to effect hardening is somewhat longer.
Other oxidizing agents of a type commonly employed in the photographic art can be used in lieu of the potassium ferrocyanide and in this connection mention is made of such materials as ammonium and alkali metal persulfates, organic peroxides, metal perchlorates and the like. In fact, it has been my experience that any type of oxidizing agent can be used for the purpose of practicing the invention provided it does not have a destructive action on the hardened gelatinor the dye used in forming the colored image.
Color development of the hardened gelatin image can be achieved by means other than by the coupling reaction between the oxidation products of p-phenylenediamine color developers and the color coupling component. Thus, in place of a color developer, there'may be substituted diazonium salts, aldehydes, sulfo hydrazides and the like, all of which react with the color coupler to produce a colored dye. Furthermore, these compounds, unlike the p-phenylenediamine color developers, do not require the presence of an oxidizing agent since they react directly with the color forming component.
The color forming components of the type suitable for practicing the invention are depicted by the following general formulae:
C-Ra
III
In Formula I, R is halogen, i.e., bromine, chlorine, iodine or the like, nitro, sulfo, or an arsonic acid radical, R is hydrogen, alkyl or a mononuclear carbocyclic aromatic radical such as phenyl, nitrophenyl, aminophenyl, stearoylaminophenyl, octadecanesulfoamidophenyl, chlo rophenyl, tolyl, anisyl and the like, R is hydrogen, --COOH or -CONHR and R is a sulfonated aliphatic radical containing at least 10 carbon atoms or a sulfonated aromatic radical substituted by an aliphatic radical containing at least 10 carbon atoms.
In Formula II, R, is a hydroxy aromatic radical, the hydroxy group being directly linked to a nuclear carbon atom, such as, hydroxy naphthyl, hydroxy phenyl and the like and such. radicals substituted by halogen, i.e., chlorine, bromine and the like, sulfo carboxy, lower alkyl, i.e., alkyl containing up to five carbon atoms, such as, methyl, ethyl, propyl, butyl and amyl, and lower alkoxy, the alkyl radical of which is as above, R is a long aliphatic chain containing at least ten carbon atoms, such as,
3 A 4 decyl, lauryl, oleyl, octadecyl and the like and R is a COMPOUND 6 water solubihzmg group, such as, sulfo, cal-boxy, .hy- 1 0ctadecyl 2 (2, (1, Hydmxy)NaPhthYDBem droxy, hydroxy polyethenoxy ether radical and the like.
In Formula III, R has the value given above, R is zlmldazoleJ'sulfomq hydrogen or aliphatic acyl, e.g., acetyl, propionyl, bu- 5 tyryl, valeryl, capronyl, heptanoyl, caproyl, pelargonyl, i 0H undecylyl, lauroyl, myristoyl, steamy], etc., R represents a J-acid radical and A represents an arene radical, i.e., C p-phenylene, 1,4-naphthalene, etc. Hso Examples of compounds of the type embraced by 10 N Formula I are the following:
COMPOUND l COMPOUND 7 I 6-Slear0ylamino-2-(2-Phenyl-6-Br0mo-8-Hydroxy- 1 0 d l 2-(2'-(1 '-Hydroxy-4'-Chloro)Naphthyl) cinchoninoyl)Aminot0luene-4-Sulfonic Acid Benzimidazole 5 sulfonic Acid CH 9 r i h---N N-c-cm N OH (I H80 'smH V N i COMPOUND 2 COMPOUND 8 Z-Phenyl-6-Chl0ro-8-Hydr0cinchoninoyloctadecyli marine Benzimidazole-S-Sulfonic Acid 0 CIHASOQI C-N--C15Ha1 (IHEHW N 0H 01 Q C N use I N/ OH COMPOUND 3 S0111 6-Dec0xy-3-(Z-Phenyl-6-Bromo-8-Hydroxycinchoninoyl) 40 COMPOUND 9 Ammobenzenesulfomc 1-0leyl-2-(2'-(1'-Hydraxy)NaphthyDBenzimidi (I? I}! azole-S-Sulfonic Acid C N CuHu Br O-GmHn N\ OH sonar 0 5 N Hsofl H N COMPOUND 4 COMPOUND 10 1-0Ieyl-2- (2"-(1 -Hydroxy-4-Chl0r0)Naphlhyl) Benzimidazole-5-Sulfonic Acid 2- (3-Stearoylamin0phenyl)-6-Br0m0-8-Hydroxycinchoninic Acid 7 C O OH fl) 65 CiBHll Br NEG-(M z:
1 0H N C COMPOUND 5 l 2- (3-0ctadecanesulfonamidophenyl) -6-Broma- 8-Hydroxycinchoninic Acid C MPOUND 11 C o OH 1-0ctddecyl- -(2'-(1'-Hydroxy-6'-Methyl)Phenyl) 0 0 BenzimidazoIe-S-Sulfonic Acid B- IlIHs- CH" |8 a7 v 0H C CH; HSO Examples of compounds of the type included under N Formula II are the following:
COMPOUND 12 l-Lauryl- 2-(2'-(1'-Hydroxy)Naphthyl)BenzimidazoIe-S-Sulfonic Acid 111 on v .\C noas- N/ COMPOUND 13 1-Octadecyl-2-(2'-(1 '-Hydroxy-6'-Meth0xy )Phenyl) Benzimidazole-S-Sulfonic Acid COMPOUND 14 1 -0leyl-2- (2- (1 -Hydroxy)NaphthyDBenzimidazole-S-Carboxylic Acid I on: Q U \C 11000 N/ Examples of compounds of the type included within the ambit of Formula III are the following:
COMPOUND 15 7 OH O la av Hogs N/COE COMPOUND 16 SOaH COCHs' HOaS COMPOUND 17 OH (llia a-l COMPOUND 18 HOaS OCzHs SOaH HOaS- 6 COMPOUND 19 OH CmHn CnHns COMPOUND 20 COMPOUND 21 Cu a I l a \C Nmsom H98 9 860GB:
It is to be noted that the aforelisted color couplers con tain a long aliphatic chain, the purpose of which is to prevent diffusion or migration of such compounds when they are incorporated in a multilayer photographic element. For the most part, the color couplers disclosed herein are known compounds and their preparation and prop erties are given in the chemical literature. Thus, compounds of Formulae I and II are referred to respectively in U.S. Patents 2,524,741 and 2,530,349.
Couplers of the type embraced by formula III, while i not specifically referred to in the literature, can be pre pared by conventional methods known to the art. These compounds can be synthesized by reacting a 4'- carboxyaryl-I-acid with an o-phenylenediamine of the following formula:
wherein R and R have the values given above, the method used being generally that disclosed in the aforementioned U.S. Patent 2,530,349. The carboxyarylI-acids are described in U.S.P. 2,591,642.
The p-phenylenediamine color developers, the oxidation products of which are used to couple with the couplers as set forth herein, are so well known in the photographic art that it is considered unnecessary to describe these materials in detail.
I have also ascertained that azine developing agents can also be used for practicing my invention. The azinc developing agents are aromatic triamines which on color development with appropriate couplers give rise to phenazonium dyestutf images. Such color developers are also well known in the art and in this connection reference is made to the following U.S. patents: 2,486,440, 2,522,802, 2,569,906, 2,570,116, 2,537,460.
In some instances, it may be undesirable to use an oxidizing agent in which case the p-phenylenediamine or azine developing agents can be replaced by an aromatic diazonium compound in order to form a colored image by coupling with a color forming component in order to produce the colored, hardened gelatin images. Such aromatic diazonium com-pounds usually employed in the form of their stable diazonium sulfates, chlorobenzene sulfonates, chlorfluorides, etc., are known chemical compounds. In general, such diazonium compounds are prepared by diazotization of aromatic amines by the well known procolor aspects of the subject.
cedure of diazotizing the particular amine with sodium nitrite in the presence of an acid. For a comprehensive treatise on the diazotization of aromatic amines, reference is made to The Aromatic Diazo Compounds and Their Technical Applications, 2nd edition, 1949, by Saunders.
The method of producing hardened gelatin images as described herein is compatible with ancillary gelatin hardening agents and I have, in fact, ascertained that my hardening process can be augmented by such well known gelatin hardeners as the alkali metal dichromates, silver, silver salts and the like.
My method of forming colored, hardened gelatin images is eminently suitable for reproducing the colored aspects of a subject. Thus, a light sensitive photographic element, prepared in accordance with the present invention, is exposed to one of the primary colored aspects of a subject as represented for instance by a color separation negative or positive. The resulting exposed and hardened gelatin image is then subtractively dyed and developed in accordance with the methods set forth above. Similarly prepared photographic elements are then exposed to the remaining color aspects of the subject and dyed with the appropriate subtractive dye. The resulting subtractively dyed color aspects are then placed in register which is then viewed through a white light source in order to reconstruct the complete color aspects of the subject.
In place of making physically separate coatings for each primary color aspect of the subject as above, a single photographic element can be used to record the In this method, a photographic element is prepared by the previous method and exposed and the image of hardened gelatin subtractively dyed to one of the color aspects of the subject. After removal of the unhardened gelatin in the non-irradiated areas, the same photographic element is given a second coating, exposed, subtractively dyed in order to record a second primary color aspect of the subject. The process of coating, exposing and dyeing is then repeated until all of the remaining color aspects of the subject have been reproduced. In this manner, all of the colors of the subject are thus recorded on a single layer. This method has the advantage that once the color aspects are recorded, the problem of keeping three physically sep arate reproductions in register is eliminated.
My colored, hardened photographic images can be formed on a wide variety of surfaces including transparent, translucent and opaque supports such as ceramic ware, paper, glass, plastic, etc.
The following examples are given in order to illustrate the invention in greater detail. It is to be understood, however, that these examples are given by way of illustration only and are not to be taken as limiting the invention.
EXAMPLE I 1 gram of the compound CnHn was dissolved in 100 ml. of 3% gelatin and coated on a white opaque support to yield a coating of approximately 2-6 M. The coating thus obtained was exposed through a pattern such as a silver negative to ultraviolet radiation emanating from the lamp in a White Print Machine at slow speed (4 passes). The resulting exposed coating was then treated in the following manner:
A. A section of the coating was immersed in a p-N,N- dialkylaminoaniline type colordeveloper solution for 1-2 minutes. This was followed by immersing the coating in a potassium ferricyanide oxidizing bath for several minutes. As a result of this treatment. an indiscriminant color coupling occurred throughout the film. The coating was then bathed in warm water (40-50 C.). The unhardened gelatin plus dye in the unexposed areas was thus removed by washing and a positive blue-green dye plus gelatin image remained in the areas exposed to radiation.
B. A section of the exposed coating was bathed in a solution of diazotized sulfanilic acid which was adjusted to a pH of about 6 with acetic acid. Color coupling again occurred indiscrimin-antly to yield a red dye. The processed coating was then washed as before to yield a positive red azo dye plus gelatin image in the regions hardened by exposure.
The color developer formulation used above had the following composition:
EXAMPLE II A coating was made the manner described in Example I with the exception that instead of the hardening compound used therein a hardening compound having the formula 1sHa1 it E so H 3 was used. The film was exposed as in Example I and the exposed coating was treated in the following manner:
A. A section of the exposed coating was immersed in a color developing solution containing a 6-phenylamino-4- dimethylaminometanilic acid type as a color developer. The coating was then processed in a ferricyanide oxidizing bath as before to yield an overall blue-green azine dye. The processed strip was then washed as in Example I to yield a positive hardened gelatin plus blue-green azine dye in the exposed areas of the film.
B. A section of the exposed film was bathed in diamtized sulfanilic acid and treated as in Example IB to yield a reddish magenta azo positive dye image.
The developer formulation used above was the same as given in Example I of U.S.P. 2,522,802 except that an equivalent amount of 6-phenylamino-4-dimethylaminometanilic acid was used in place of the developing agent of the example of the patent.
EXAMPLE III A coating was prepared as in Example I using the hardening compound instead of the hardening compound of Example I. The material was then treated as in Example IIA. A magenta azine dye image was produced.
EXAMPLE iv 9 s' the greatest hardening in the gelatin next to the base which promotes better adhesion of the hardened gelatin to the base.
EXAMPLE v A coating of 0.5 g. of 3-(1-hydroxy-2-naphthoyl) N'-octadecylamidoisophthalic acid and 0.5 g. of sodium dichromate in 100 ml. of 3% gelatin was coated on transparent film base. The material was exposed through the base and developed as in Example I. In this case, a bluish-green dye image is obtained with p-phenylenediamine type developer and an orange with-diazotized sulfanilic acid.
My invention is not limited to the detailed description thereof contained herein, but includes all modifications that fall within the scope of the appended claims.
I claim:
1. A radiation sensitive photographic element comprising a base and a radiation sensitive coating thereon, said coating being free of silver halide and consisting essentially of gelatin and a color coupler selected from those represented by the following general formulae:
wherein R is a member selected form the class consisting of halogen, nitro, sulfo and arsonic acid radicals, R is a member selected from the class consisting of hydrogen,
, alkyl and a mononuclear carbocyclic aromatic radical, R
is a member selected from the class consisting of H, COOH and CONH-R and R, is a member selected from the class consisting of sulfonated aliphatic radicals containing at least 10 carbon atoms and sulfonated aromatic radicals substituted by an aliphatic radical containing at least 10 carbon atoms; R; is a water solubilizing group, R is an hydroxy aromatic radical, the hydroxy group being nuclearly attached and said radical being linked to the benzimidazole radical in the ortho position to said hydroxy group, R is a long aliphatic chain capable of rendering said compound fast to diffusion in a photographic colloid, R, is a member selected from the class consisting of hydrogen and aliphatic acyl radicals, R7 represents a I-acid radical and A- is an arylene group selected from the class consisting of a p-phenylene radical and a naphthylene radical.
2. The product asr'ecited in claim 1 wherein the base is transparent.
3. The product as recited in claim 1 wherein the base is opaque.
10 4. The product as recited in claim 1 wherein the coupler is represented by the following formula:
N osH 5. The product as recited in claim 1 wherein the color coupler is represented by the following general formula:
7. The product as recited in claim 1 wherein the color coupler is represented by the following formula:
OH H a:
SOaH H0:
8. A method of producing a hardened gelatin colored photographic reproduction which comprises exposing to an optical image a radiation sensitive photographic element comprising a base and a radiation sensitive coating thereon, said coating consisting essentially of gelatin and a color coupler selected from those represented by the following general formulae:
wherein R is a member selected from the class consisting of halogen, nitro, sulfo and arsonic acid radicals, R is a member selected from the class consisting of hydrogen, alkyl and a mononuclear carbocyclic aromatic radical, R is a member selected from the class consisting of H, COOH and CONHR and R is a member selected from the class consisting of sulfonated aliphatic radicals containing at least 10 carbon atoms and sulfonated aromatic radicals substituted by an aliphatic radical containing at least 10 carbon atoms; R is a water solubilizing group, R is a hydroxy aromatic radical, the hydroxy group being nuclearly attached and said radical being linked to the benzimidazole radical in the ortho position to said hydroxy group, R is a long aliphatic chain capable of rendering said compound fast to diffusion in a photographic colloid, R; is a member selected from the class consisting of hydrogen and aliphatic acyl radicals, R represents a J-acid radical and A-- is an arylene group selected from the class consisting of a p-phenylene radical and a naphthylene radical, hardening by said exposure the gelatin layer in the exposed areas treating the exposed photographic element with a primary aromatic amino color developer in the presence of a water soluble oxidizing agent in order to effect color coupling between the said color coupler and said color developer, removing by washing the unexposed and unhardened gelatin in the unexposed areas of the coating thereby leaving a colored, hardened gelatin relief image corresponding to the exposed areas.
9. The process as defined in claim 8 wherein the base is transparent.
- 10. The process as defined in claim 8 wherein the base is opaque.
11. The' process as defined in claim 8 wherein the pphenylenediamine color developer contains in the position ortho to the free amino group an amino group having at least one free hydrogen.
12. The process as defined in claim 8 wherein the coupler is represented by the following formula:
C ONE-- 12 13. The process as defined in claim 8 wherein the color coupler is represented by the fOllOWing general formula:
- I l 0H \C Hols N/ 15. -The process as defined in claim 8 wherein the color coupler is represented by the following formula:
OH (IJisHu Ill N\ N C SOaH HO S 16. The method as defined by claim 8 wherein the light used in exposing the photographic element to an optical image is provided by an ultraviolet light source;
References Cited in the file of this patent UNITED STATES PATENTS 2,386,167 Murray .Q Oct. 2, 1945 2,426,984 McQueen Sept. 2, 1947 2,522,802 Sargent et a1. Sept. 19, 1950 2,524,741 Tulagin et al. Oct. 3, 1950 2,530,349 Craig Nov. 14, 1950 2,570,116 Gunther Oct. 2, 1951 2,591,642 Tulagin et a1. Apr. 1, 1952 2,623,821 1952 'Isherwood et a1. Dec. 30,
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,099,559 July 30, 1963 Robert F. Coles It is hereby certified that error appears in the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.
Column 3, "COMPOUND 2", in the heading, for "Hydrocinchoninoyloctadecyltaurine", in italics, read Hydroxycinchoninoyloctadecyltaurine in italics; column 6, line 39, for "to read in column 9, line 52, for "form" read from column 10, lines 31 to 38, the formula should appear as shown below instead of as in the patent:
column 12, line 43, for "2,426,984" read 2,426,894
Signed and sealed this 16th day of June 1964,
(SEAL) Attest:
ERNEST W. SWIDER EDWARD J, BRENNER Attesting Officer Commissioner of Patents

Claims (1)

1. A RADIATION SENSITIVE PHOTOGRAPHUC ELEMENT COMPRISING A BASE FREE OF RADIATION SENSITIVE THEREON, SAID COATING BEING FREE OF SILVER HALIDE AND CONSISTING ESSENTIALLY OF GELATIN AND A COLOR COUPLER SELECTED FROM THOSE REPRESENTED BY THE FOLLOWING GENERAL FORMULAE:
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3248220A (en) * 1961-11-22 1966-04-26 Grinten Chem L V D Two-component diazotype material
US3282693A (en) * 1960-02-05 1966-11-01 Eastman Kodak Co Photographic printout methods and materials utilizing organic azide compounds and coupler compounds therefor
US3294542A (en) * 1963-12-23 1966-12-27 Keuffel & Esser Co Photosensitive diazo compositions
US3499902A (en) * 1967-08-09 1970-03-10 Minnesota Mining & Mfg Organic hydrazone compound containing azo coupler moiety

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Publication number Priority date Publication date Assignee Title
US2386167A (en) * 1943-08-28 1945-10-02 Du Pont Photographic article of manufacture
US2426984A (en) * 1940-10-30 1947-09-09 Jeannette Hoehne Expanding hose reel
US2522802A (en) * 1948-12-22 1950-09-19 Gen Aniline & Film Corp Production of yellow dye images by color development
US2524741A (en) * 1946-01-10 1950-10-03 Gen Aniline & Film Corp Magenta phenazonium dyestuff images from 6-substituted-8-hydroxyquinoline couplers
US2530349A (en) * 1947-04-30 1950-11-14 Gen Aniline & Film Corp Cyan color formers capable of yielding fine grain images
US2591642A (en) * 1950-01-10 1952-04-01 Gen Aniline & Film Corp Nondiffusing color formers comprising aryl j-acids in which the aryl radical is provided with a nondiffusing group
US2623821A (en) * 1948-07-14 1952-12-30 Calico Printers Ass Ltd Photographic development of color on textile and other materials

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* Cited by examiner, † Cited by third party
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US2426984A (en) * 1940-10-30 1947-09-09 Jeannette Hoehne Expanding hose reel
US2386167A (en) * 1943-08-28 1945-10-02 Du Pont Photographic article of manufacture
US2524741A (en) * 1946-01-10 1950-10-03 Gen Aniline & Film Corp Magenta phenazonium dyestuff images from 6-substituted-8-hydroxyquinoline couplers
US2570116A (en) * 1946-01-10 1951-10-02 Gen Aniline & Film Corp Color developers for the production of azine dye images
US2530349A (en) * 1947-04-30 1950-11-14 Gen Aniline & Film Corp Cyan color formers capable of yielding fine grain images
US2623821A (en) * 1948-07-14 1952-12-30 Calico Printers Ass Ltd Photographic development of color on textile and other materials
US2522802A (en) * 1948-12-22 1950-09-19 Gen Aniline & Film Corp Production of yellow dye images by color development
US2591642A (en) * 1950-01-10 1952-04-01 Gen Aniline & Film Corp Nondiffusing color formers comprising aryl j-acids in which the aryl radical is provided with a nondiffusing group

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3282693A (en) * 1960-02-05 1966-11-01 Eastman Kodak Co Photographic printout methods and materials utilizing organic azide compounds and coupler compounds therefor
US3248220A (en) * 1961-11-22 1966-04-26 Grinten Chem L V D Two-component diazotype material
US3294542A (en) * 1963-12-23 1966-12-27 Keuffel & Esser Co Photosensitive diazo compositions
US3499902A (en) * 1967-08-09 1970-03-10 Minnesota Mining & Mfg Organic hydrazone compound containing azo coupler moiety

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