US3033677A - Photographic processes utilizing photolytic halogen - Google Patents

Photographic processes utilizing photolytic halogen Download PDF

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US3033677A
US3033677A US821427A US82142759A US3033677A US 3033677 A US3033677 A US 3033677A US 821427 A US821427 A US 821427A US 82142759 A US82142759 A US 82142759A US 3033677 A US3033677 A US 3033677A
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photolytic
dye
layer
halogen
image
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US821427A
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Thomas I Abbott
Edward C Yackel
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Eastman Kodak Co
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Eastman Kodak Co
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    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/494—Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
    • G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
    • G03C5/50—Reversal development; Contact processes

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  • the invention involves exposing imagewise a layer containing a compound which releases photolytic halogen upon exposure to light, in the presence of a substance changing color upon oxidation by the halogen.
  • One embodiment of the invention includes exposing a photographic silver halide emulsion layer so as to release a photolytic halogen imagewise and using the resultant halogen through an oxidation reaction, to produce a visible image.
  • photolytic halogen e.g. halogen released upon exposure of silver halide to light
  • photolytic halogen was capable of effecting an imagewise change in color of a layer of dye such as fiuorescein. This was demonstrated by exposure of a film having a layer of silver bromide, in contact with a sheet impregnated with fluorescein dye with the result that as the bromine was released from the silver bromide in the region of exposure, it diffused to the fluorescein dye layer and oxidized the dye to a purple image.
  • the dye was replaced with other compositions which responded with a color change on oxidation, such as starch-iodide, a similar result was obtained.
  • a preferred process of our invention utilizing photolytic bromine and leuco bases of dyes embodies a lightsensitive element comprising a hydrophilic organic colloid layer containing silver halide, leuco base and polymeric materials adapted to control the formation of the photolytic halogen image.
  • a lightsensitive element comprising a hydrophilic organic colloid layer containing silver halide, leuco base and polymeric materials adapted to control the formation of the photolytic halogen image.
  • the resultant dye image is transferred to a reception layer by thermographic means.
  • a dispersion of silver bromide in a hydrophilic organic colloid such as gum arabic is exposed imagewise in the presence of a polyalkylene oxide such as Carbowax 4000 and in the presence of a soft acrylate polymer dispersion and a leuco base.
  • the photolytic halogen generated by exposure of the silver bromide to light oxidizes the leuco base to a dye.
  • the exposed layer is heated in contact with a reception sheet, the dye image dissolved in the polyalkylene oxide transfers imagewise to the sheet yielding a negative reproduction of the subject.
  • Example 1 The following composition was prepared. To 5 cc. of a 25 percent aqueous dispersion of percent polyethylacrylate and 10 cercent polyacrylonitrile was first added with stirring 10 cc. of water followed by 10 cc. of an emulsion prepared by adding 50 cc. of 1 N silver nitrate and 50 cc. of 1 N potassium bromide to 60 cc. of 2 percent aqueous gum arabic solution. Thereafter 5 cc. of a 30 percent aqueous solution of Carbowax 4000 (polyethylene oxide of approximate molecular weight 4000) and 2 cc. of a 3.3 percent solution of leuco Malachite Green in ethyl alcohol was added.
  • Carbowax 4000 polyethylene oxide of approximate molecular weight 4000
  • the resulting composition was coated upon a paper support which had previously been rendered water-resistant by coating with a cellulose ester.
  • the resultant sensitive element is shown in stage 1 of the drawings wherein layer 10 represents the support carrying the sensitive layer 11 prepared as described above. After drying the sensitive element was exposed in area 12 under a line negative for 20 seconds using a photoflood lamp at a distance of 8 inches. A green dye image appeared in the exposed area 12- as shown in stage 2 of the drawing. The exposed layer was then placed in contact with a paper reception sheet and the sandwich heated for 2 seconds at approximately 80 C.
  • the leuco base may be replaced by other leuco bases such as leuco Pararosaniline, leuco Auramine, etc.
  • the Carbowax 4000 may be replaced by similar amounts of other polyalkylene oxides such as polypropylene oxide and polybutylene oxides.
  • the lower mol-uecular weight polyalkylene oxides containing an average of from about 35 to alkoxyl units in the polymer chain, are best suited to the process since they more readily facilitate transfer of the dye image to the reception sheet.
  • the acrylic polymers of the sensitive element may be prepared in a well-known manner by polymerization in water of alltyl acrylates such as methylacrylate, ethylacrylate, methylmethacrylate in the presence of a dispersing agent alone or together with other acrylic monomers including acrylonitrile so as to obtain hydrosol dispersions of the soft, water insoluble acrylate polymers suited to the process.
  • a film carrying an internal latent image silver halide emulsion such as described in Davey et al. US. Patent 2,592,250.
  • a photographic paper base which had been dipped in an aqueous solution containing 5 percent soluble starch and 1 percent potassium iodide.
  • Coating A was soaked for 30 seconds in distilled water and held in contact with B in a photographic printing a frame with the emulsion in contact with the starch layer while exposure was made by a photoflood lamp 8 inches above a line positive.
  • Example 3 A water resistant paper base was coated with the following composition:
  • the coated paper was used in the process of Example 2 in place of film B with the result that the image produced in this experiment was cyan in color and positive by Virture of dye bleaching in the areas in which photolytic halogen oxidized the potassium iodide to iodine.
  • a film carrying a fine-grain silver chloride emulsion A film carrying a fine-grain silver chloride emulsion.
  • Coating B was fogged by exposing it for 4 seconds to a photofiood lamp at a distance of 8 inches.
  • Coatings A and B were each immersed in distilled water for 30 seconds and placed together as described in Example 2 and exposed in like manner.
  • coating B was placed for 1 minute in a conventional silver halide developing solution, rinsed in running water and fixed. A positive image of high density and very low background was obtained in film B. The photolytic halogen formed in the exposed areas had removed the latent image from the fogged silver chloride emulsion.
  • Example 1 The use in the invention of an organic compound releasing halogen upon exposure to light is illustrated by this example. The following elements were provided:
  • Elements A and B were exposed 20 seconds to a photofiood lamp at 6 inches through a line subject. A green image was obtained only in A. When the geltain layer of A thus exposed was removed with warm water a green image remained in the support.
  • a photographic process which comprises exposing to a subject a supported layer of a mixture of, a soft water-insoluble acrylate polymer of the class consisting of alkyl acrylate and alkyl methacrylate polymers, a polyalkylene om'de, a leuco base of a triphenylmethane dye soluble in said polyalkylene oxide and silver bromide, until an appreciable amount of photolytic bromine has been released from the exposed silver bromide and has oxidized the leuco base to a dye in the region of exposure, heating the layer in contact with a reception sheet to transfer at least a portion of the dye imagewise from the layer to the sheet.

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

Description

May 8, 1962 T. l. ABBOTT ETAL 3,033,677
PHOTOGRAPHIC PROCESSES UTILIZING PHOTOLYTIC HALOGEN Filed June 19, 1959 srage EXPOSURE l l l /2 SILVER BROMIDE, LE UOODASE,
POLmLK YLE IVE OXIDE, AORYLA TE POLYMER /0 /-suPP0/?r THOMAS ABBOTT EDWARD O. VAC/(EL INVENTORS BY flax/M ATTORNEY 8A6E/V7' United States Patent Ofilce 3,033,677 Patented May 8, 1962 This invention relates to photographic processes utilizing photolytic halogen to bring about the formation, and more particularly, the thermographic transfer of a colored image.
The invention involves exposing imagewise a layer containing a compound which releases photolytic halogen upon exposure to light, in the presence of a substance changing color upon oxidation by the halogen.
One embodiment of the invention includes exposing a photographic silver halide emulsion layer so as to release a photolytic halogen imagewise and using the resultant halogen through an oxidation reaction, to produce a visible image.
In a search for a practical photographic reproduction process utilizing photolytic halogen (e.g. halogen released upon exposure of silver halide to light) for the formation of a colored image, it was found that photolytic halogen was capable of effecting an imagewise change in color of a layer of dye such as fiuorescein. This was demonstrated by exposure of a film having a layer of silver bromide, in contact with a sheet impregnated with fluorescein dye with the result that as the bromine was released from the silver bromide in the region of exposure, it diffused to the fluorescein dye layer and oxidized the dye to a purple image. When the dye was replaced with other compositions which responded with a color change on oxidation, such as starch-iodide, a similar result was obtained.
in a similar manner, it was found that a silver bromide emulsion layer could be exposed to an image in the presence of a leuco base with the result that the photolytic bromine released from the silver bromide oxidized the leuco base to the dye. This was demonstrated in one case by coating a gelatino-silver bromide emulsion containing leuco Malachite Green on a cellulose ester surface, such as paper coated with cellulose ester, followed by wetting the emulsion layer and exposing it to a subject for a time sufficient to yield photolytic bromine imagewise which oxidized the leuco base to the dye. Upon removal of the emulsion with warm water, a green dye image was found on the cellulose ester surface. A rnagenta image was obtained in a similar manner by use of leuco Pararosaniline.
A preferred process of our invention utilizing photolytic bromine and leuco bases of dyes, embodies a lightsensitive element comprising a hydrophilic organic colloid layer containing silver halide, leuco base and polymeric materials adapted to control the formation of the photolytic halogen image. Upon oxidation of the leuco base by the photolytic halogen the resultant dye image is transferred to a reception layer by thermographic means.
The accompanying drawing shows in greatly enlarged cross-sectional view a representative sensitive element useful in the preferred process of the invention and the various stages of the process of obtaining a photographic reproduction t. erefrom.
In this preferred process of the invention, a dispersion of silver bromide in a hydrophilic organic colloid such as gum arabic is exposed imagewise in the presence of a polyalkylene oxide such as Carbowax 4000 and in the presence of a soft acrylate polymer dispersion and a leuco base. The photolytic halogen generated by exposure of the silver bromide to light oxidizes the leuco base to a dye. When the exposed layer is heated in contact with a reception sheet, the dye image dissolved in the polyalkylene oxide transfers imagewise to the sheet yielding a negative reproduction of the subject.
The following examples will serve to illustrate our invention.
Example 1 The following composition was prepared. To 5 cc. of a 25 percent aqueous dispersion of percent polyethylacrylate and 10 cercent polyacrylonitrile was first added with stirring 10 cc. of water followed by 10 cc. of an emulsion prepared by adding 50 cc. of 1 N silver nitrate and 50 cc. of 1 N potassium bromide to 60 cc. of 2 percent aqueous gum arabic solution. Thereafter 5 cc. of a 30 percent aqueous solution of Carbowax 4000 (polyethylene oxide of approximate molecular weight 4000) and 2 cc. of a 3.3 percent solution of leuco Malachite Green in ethyl alcohol was added. The resulting composition was coated upon a paper support which had previously been rendered water-resistant by coating with a cellulose ester. The resultant sensitive element is shown in stage 1 of the drawings wherein layer 10 represents the support carrying the sensitive layer 11 prepared as described above. After drying the sensitive element was exposed in area 12 under a line negative for 20 seconds using a photoflood lamp at a distance of 8 inches. A green dye image appeared in the exposed area 12- as shown in stage 2 of the drawing. The exposed layer was then placed in contact with a paper reception sheet and the sandwich heated for 2 seconds at approximately 80 C. Upon separation of the two sheets, it was found that a portion of the green dye image had transferred to the paper to provide a sharp image of the subject shown in stage 3 wherein layer 13 represents the paper reception sheet and image 14 the green dye image which had transferred thereto. The stability of this dye print was tested by exposing it to a high intensity light source which resulted in the background areas remaining white indicating that in the transfer step no silver halide had transferred.
In the above process the leuco base may be replaced by other leuco bases such as leuco Pararosaniline, leuco Auramine, etc. The Carbowax 4000 may be replaced by similar amounts of other polyalkylene oxides such as polypropylene oxide and polybutylene oxides. The lower mol-uecular weight polyalkylene oxides containing an average of from about 35 to alkoxyl units in the polymer chain, are best suited to the process since they more readily facilitate transfer of the dye image to the reception sheet.
The acrylic polymers of the sensitive element may be prepared in a well-known manner by polymerization in water of alltyl acrylates such as methylacrylate, ethylacrylate, methylmethacrylate in the presence of a dispersing agent alone or together with other acrylic monomers including acrylonitrile so as to obtain hydrosol dispersions of the soft, water insoluble acrylate polymers suited to the process.
Another photographic reproduction process utilizing photolytic'halogen for effecting a color change in contiguous oxidizable substances is as follows:
Example 2 The following elements were provided:
A. A film carrying an internal latent image silver halide emulsion such as described in Davey et al. US. Patent 2,592,250.
B. A photographic paper base which had been dipped in an aqueous solution containing 5 percent soluble starch and 1 percent potassium iodide.
Coating A was soaked for 30 seconds in distilled water and held in contact with B in a photographic printing a frame with the emulsion in contact with the starch layer while exposure was made by a photoflood lamp 8 inches above a line positive.
After separating of the elements, a purplish image was formed which is characteristic of the color of the starch iodine complex. The exposure produced photolytic halogen which oxidized the potassium iodide producing iodine which reacted with the starch to form the color.
Example 3 A water resistant paper base was coated with the following composition:
0.1 g. [1,1-diethyl-4,4'-carbocyanine iodide] dissolved in 10 cc. methyl alcohol added to 40 cc. 3 percent aqueous photographic gelatin solution containing 1 percent potassium iodide.
The coated paper was used in the process of Example 2 in place of film B with the result that the image produced in this experiment was cyan in color and positive by Virture of dye bleaching in the areas in which photolytic halogen oxidized the potassium iodide to iodine.
Example 4 Two films were provided as follows:
A. A film such as film A of Example 2.
B. A film carrying a fine-grain silver chloride emulsion.
Coating B was fogged by exposing it for 4 seconds to a photofiood lamp at a distance of 8 inches.
Coatings A and B were each immersed in distilled water for 30 seconds and placed together as described in Example 2 and exposed in like manner.
After separating A and B, coating B was placed for 1 minute in a conventional silver halide developing solution, rinsed in running water and fixed. A positive image of high density and very low background was obtained in film B. The photolytic halogen formed in the exposed areas had removed the latent image from the fogged silver chloride emulsion.
Example The use in the invention of an organic compound releasing halogen upon exposure to light is illustrated by this example. The following elements were provided:
A. 0.1 g. of leuco Malachite Green in 10 ml. of ethyl alcohol and 0.05 g. of 2-iodo-1,3-diphenyl-1,3-propanedione in 10 ml. ethyl alcohol were added to 50 ml. of 4 percent aqueous gelatin solution and the final solution coated upon a water resistant paper support at a coverage of 5.6 ml. per sq. ft.
B. Same as A but the iodo compound omitted.
Elements A and B were exposed 20 seconds to a photofiood lamp at 6 inches through a line subject. A green image was obtained only in A. When the geltain layer of A thus exposed was removed with warm water a green image remained in the support.
What we claim is:
l. A photographic process which comprises exposing to a subject a supported layer of a mixture of, a soft water-insoluble acrylate polymer of the class consisting of alkyl acrylate and alkyl methacrylate polymers, a polyalkylene om'de, a leuco base of a triphenylmethane dye soluble in said polyalkylene oxide and silver bromide, until an appreciable amount of photolytic bromine has been released from the exposed silver bromide and has oxidized the leuco base to a dye in the region of exposure, heating the layer in contact with a reception sheet to transfer at least a portion of the dye imagewise from the layer to the sheet.
2. The process of claim 1 wherein the transfer of dye imagewise from the layer to the reception sheet is followed by heating the layer in contact with another reception sheet to transfer a further portion of the dye imagewise to the sheet.
3. The process of claim 1 wherein the polyalkylene oxide is polyethylene oxide.
References Cited in the file of this patent UNITED STATES PATENTS 2,543,181 Land Feb. 27, 1951 2,784,091 Carroll et al Mar. 5, 1957 2,892,710 Cohler et a1 June 30, 1959 2,909,430 Rogers Oct. 20, 1959 FOREIGN PATENTS 212,177 Australia Jan. 3, 1958 790,811 Great Britain Feb. 9', 1958 498,871 Great Britain Jan. 10, 1939 OTHER REFERENCES Mees: The Theory of the Photographic Process, 2nd ed, The Macmillan Company, New York, 1954, pages 584-589.

Claims (1)

1. A PHOTOGRAPHIC PROCESS WHICH COMPRISES EXPOSING TO A SUBJECT A SUPPORTED LAYER OF A MIXTURE OF, A SOFT WATER-INSOLUBLE ACRYLATE POLYMER OF THE CLASS CONSISTING OF ALKYL ACRYLATE AND ALKYL METHACRYLATE POLYMERS, A POLYALKYLENE OXIDE, A LEUCO BASE OF A TRIPHENYLMETHANE DYE SOLUBLE IN SAID POLYALKYLENE OXIDE AND SILVER BROMIDE UNTIL AN APPRECIABLE AMOUNT OF PHOTOLYTIC BROMIDE HAS BEEN RELEASED FROM THE EXPOSED SILVER BROMIDE HAS OXIDIZED THE LEUCO BASE TO A DYE IN THE REGION OF EXPOSURE, HEATING THE LAYER IN CONTACT WITH A RECEPTION SHEET TO TRANSFER AT LEAST A PORTION OF THE DYE IMAGEWISE FROM THE LAYER TO THE SHEET.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3102810A (en) * 1961-04-05 1963-09-03 Horizons Inc Print-out cyanine and styryl dye bases and process of producing litho masters and the like therewith
US3275437A (en) * 1963-01-24 1966-09-27 Du Pont Image transfer process and elements therefor
US3305361A (en) * 1962-12-28 1967-02-21 Gen Electric Information recording
US3309991A (en) * 1961-02-07 1967-03-21 Agfa Ag Reproduction process by means of heat

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB498871A (en) * 1936-05-09 1939-01-10 Kodak Ltd Process of colour photographic development
US2543181A (en) * 1947-01-15 1951-02-27 Polaroid Corp Photographic product comprising a rupturable container carrying a photographic processing liquid
US2784091A (en) * 1953-07-01 1957-03-05 Eastman Kodak Co 4-hydroxy-6-alkyl-1, 3, 3alpha, 7-tetrazaindene stabilizers for photographic emulsions sensitized with polyalkylene esters, amides, and ethers
GB790811A (en) * 1955-02-11 1958-02-19 Agfa Ag Fur Photofabrikation Process for the production of laterally non-reversed positive copies by heat development
US2892710A (en) * 1957-07-10 1959-06-30 Polaroid Corp Photographic products and processes
US2909430A (en) * 1958-10-08 1959-10-20 Polaroid Corp Photographic processes

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB498871A (en) * 1936-05-09 1939-01-10 Kodak Ltd Process of colour photographic development
US2543181A (en) * 1947-01-15 1951-02-27 Polaroid Corp Photographic product comprising a rupturable container carrying a photographic processing liquid
US2784091A (en) * 1953-07-01 1957-03-05 Eastman Kodak Co 4-hydroxy-6-alkyl-1, 3, 3alpha, 7-tetrazaindene stabilizers for photographic emulsions sensitized with polyalkylene esters, amides, and ethers
GB790811A (en) * 1955-02-11 1958-02-19 Agfa Ag Fur Photofabrikation Process for the production of laterally non-reversed positive copies by heat development
US2892710A (en) * 1957-07-10 1959-06-30 Polaroid Corp Photographic products and processes
US2909430A (en) * 1958-10-08 1959-10-20 Polaroid Corp Photographic processes

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3309991A (en) * 1961-02-07 1967-03-21 Agfa Ag Reproduction process by means of heat
US3102810A (en) * 1961-04-05 1963-09-03 Horizons Inc Print-out cyanine and styryl dye bases and process of producing litho masters and the like therewith
US3305361A (en) * 1962-12-28 1967-02-21 Gen Electric Information recording
US3275437A (en) * 1963-01-24 1966-09-27 Du Pont Image transfer process and elements therefor

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