US3507657A - Light-developable direct-print silver halide emulsions - Google Patents

Light-developable direct-print silver halide emulsions Download PDF

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US3507657A
US3507657A US507233A US3507657DA US3507657A US 3507657 A US3507657 A US 3507657A US 507233 A US507233 A US 507233A US 3507657D A US3507657D A US 3507657DA US 3507657 A US3507657 A US 3507657A
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silver halide
emulsions
light
direct
developable
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Theodore J Kitze
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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
    • G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/49—Print-out and photodevelopable emulsions

Definitions

  • the present invention relates to photography, and more particularly, to light-developable, direct-print photographic silver halide emulsions.
  • Radiation-sensitive photographic elements adapted for light recording, e.g., oscillographic recording, are known. Typical of such photographic elements are the developingout and print-out type.
  • the developing-out type of photo graphic element requires that the exposed material be chemically developed and fixed in order to provide a stable visible image.
  • the print-out type of photographic element develops on exposure and requires no development step.
  • the print-out type is generally much slower than the developing-out type and the images are unstable and have a short life.
  • a third type of radiation-sensitive photographic element especially suitable for light-writing and oscillo graphic recording comprises a hydrophilic colloid-silver halide emulsion layer which, when exposed to a high intensity source of electromagnetic radiation, forms a latent image which can then be developed by subsequent general exposure to a second source of radiation of lower intensity.
  • Such direct-Writing or direct-print emulsions are faster than print-out emulsions and require no chemical development.
  • many of the recording photographic elements of this third type have a slow rate of photodevelopment and the background areas tend to build up to obscure the image on subsequent exposure to light at an undesirably high rate.
  • Particularly useful water-soluble thiocyanates utilized during the grain formation of the silver halide of the emulsions of the invention are alkali metal thiocyanates such as sodium thiocyanate and potassium thiocyanate.
  • the amount of water-soluble thiocyanate utilized can be widely varied depending on the effect desired, the nature of the water-soluble thiocyanate and related variables. Concentrations of about .1 to 50 grams of the thiocyanate per mole of silver halide are suitably utilized, with about 1 to 10 grams of the thiocyanate per mole of silver halide being more generally utilized.
  • Suitable organic thioether silver halide solvents that can be utilized during the grain formation of the silver halide emulsions of the invention are described in French Patent 1,368,647, issued June 22, 1964, and in copend ing McBride application Ser. No. 452,009 filed April 29, 1965.
  • Aqueous solutions of suitable organic thioether silver halide solvents utilized during the grain growth or formation of the silver halide grains of the present emulsions have a greater solubility for silver chloride than water. More specifically, such thioether silver halide solvents are those which, when utilized in aqueous solutions (60 C.) at 0.02 molar concentrations, are capable of dissolving more than twice the amount (by weight) of silver chloride than that which can be dissolved by water at 60 C.
  • the amount of thioether silver halide solvent utilized can be widely varied depending on the effect desired, the nature of the thioether utilized and related variables. Concentrations of about .1 to 50 grams of thioether per mole of silver halide are suitably utilized, with about 1 to 10 grams of thioether per mole of silver halide being more generally utilized.
  • Typical organic thioether silver halide solvents that can be suitably utilized in preparing the emulsions of the invention contain at least one moiety wherein oxygen and sulfur atoms are separated by an ethylene radical (e.g., -OCH CH --S).
  • the subject silver halide solvents have 1 to 3 thioether atoms (S) although silver halide solvents having more than 3 thioether atoms can be utilized.
  • organic thioether silver halide solvents can be represented by the formulas:
  • r and m are integers of 0 to 4; n is an integer of l to 2; k is an integer of 1 to 4; p and q are integers of 0 to 3;
  • X is an oxygen atoms (--O), a sulfur atom (S), a carbamyl radical a carbonyl radical or a carboxy radical i (O OH) R and R are ethylene oxide radicals (OCH CH Q and Z are hydroxy radicals (OH), carboxy radicals, or alkoxy radicals (-Oalkyl) wherein the alkyl group has 1 to carbon atoms; and Q and Z can also be the substituents described for X linked to form a cyclic compound.
  • Preferred organic thioether silver halide solvents suitable for forming the emulsions of the invention include compounds represented by the formulas:
  • r is an integer of 1 to 3; s is an integer of 1 to 2; R is an alkylene radical having 1 to 5 carbon atoms and is preferably ethylene '(-CH CH R is an alkyl radical having 1 to 5 carbon atoms and is preferably ethyl; and R is an alkylene radical having 1 to 5 carbon atoms and is preferably methylene (-CH).
  • Suitable silver halides include silver choride, silver bromide, silver bromoiodide, silver chloroiodide, and silver chlorobromoiodide.
  • the preferred emulsions are those wherein the silver halide contains at least 50% bromide, less than iodide and less than 50% chloride on a molar basis.
  • suitable emulsions reference is made to Davey et al., US. Patent 2,592,250, issued Apr. 8, 1952; and Glafkides, Photographic Chemistry, vol. 1, pp. 31-2, Fountain Press, London.
  • the so-called internal image emulsions are particularly useful in the invention, such having silver halide grains wherein a predominant amount of the sensitivity is internal to the grains.
  • Such internal image-forming emulsions are those which, when measured according to normal photographic techniques by coating a test portion of the emulsion on a transparent support, exposing to a light intensity scale having a fixed time between 1 1O and 1 second, bleaching 5 minutes in a 0.3% potassium ferricyanide solution at 65 F. and developing for about 5 minutes at 65 F. in Developer B below (an internaltype developed), having a sensitivity, measured at a density of 0.1 above fog, greater than the sensitivity of an identical test portion which has been exposed in the same way and developed for 6 minutes at 68 F. in Developer A below (a surface-type developer).
  • the water-soluble silver salt and the water-soluble halide are reacted to precipitate the silver halide under acidic conditions.
  • the pH of the silver halide precipitation is typically less than 6 and preferably less than 5.
  • Such acids as phosphoric, trifiuoroacetic, hydrobromic, hydrochloric, sulfur and nitric are typically utilized in the silver halide. precipitating media to maintain acidic conditions.
  • An excess of water-soluble halide is more generally used.
  • the pAg during the silver halide precipitation is more generally about 8 to 10.
  • the water-soluble thiocyanate and the thioether silver halide solvent can be added to the silver halide emulsion at any stage of the preparation thereof before the silver halide grains have attained their ultimate size and shape, such as to the colloidal material in which the silver halide is precipitated, in combination with one of the watersoluble salts utlized to form the silver halide such as with the water-soluble silver salt (e.g., silver nitrate) or with a water-soluble halide such as an alkali metal halide, to the silver halide prior to or during the ripening of the silver halide, or during one or more of such emulsion preparation steps.
  • the water-soluble silver salt e.g., silver nitrate
  • a water-soluble halide such as an alkali metal halide
  • the present silver halide emulsions can be washed after precipitation such as by the methods described in US. Patents 2,614,929 and 2,618,556.
  • the silver halide grains of the emulsions of the invention generally have an average grain size of about .1 to 10 microns, and more generally about .5 to 2 microns, in diameter.
  • silver halide emulsions are generally made with an equivalent or slight excess of halide ion present, I have found it desirable to add additional water-soluble halide, particularly iodide, to the silver halide emulsion after its precipitation but before it is coated. More generally, about .1 to 50 mole percent, and preferably about 1 to 10 mole percent of water-soluble halide based on the silver halide in the emulsion are present in the subject emulsions.
  • Illustrative water-soluble halides include the ammonium, calcium, lithium, magnesium, potassium, and sodium salts.
  • Lead ions can be used in the precipitation or formation of the silver halide used in the emulsions of the invention.
  • Water-soluble lead salts are typically added with a water-soluble silver salt to an appropriate water-soluble halide to precipitate a lead-silver halide.
  • the amount of lead used in the present silver halide emulsions typically ranges from about .01 to 5 mole percent based on the silver.
  • the use of such lead ions in the formation of the silver halide facilitates the reduction of background density (D while exhibiting increased image density (D when exposed to a high intensity light source and photodeveloped by exposure to a lower intensity light source.
  • Halogen acceptors of the type utilized in conventional light-developable, direct-print silver halide emulsions can be incorporated in the present emulsions.
  • Typical halogen acceptors that can be utilized in the emulsions of the invention include stannous chloride, thiosalicyclic acid, 1-phenyl-3-pyrazolidone, thiourea, thiosemicarbazide, 1- methyl 2-imidazolethione, l-n-butyl-l,2,5,6-tetrahydro- 1,3,5-triazine-4-thiol, D-mannose thiosemicarbazone, lphenyI-S-mercaptotetrazole, 4-thiobarbituric acid, urazole, 3-thiourazole, l-phenylurazole, 4-ethylurazole, 3- iminothiourazole and the like halogen acceptors.
  • a Wide variety of hydrophilic, water-permeable organic colloids can be suitably utilized in preparing the silver halide emulsions or dispersions of the invention.
  • Gelatin is preferably utilized although other colloidal material such as colloidal albumin, cellulose derivatives, synthetic resins or the like can be utilized.
  • Suitable colloids that can be used are polyvinyl alcohol or a hydrolyzed polyvinyl acetate as described in Lowe, US. Patent 2,286,215, issued June 16, 1942; a far hydrolyzed cellulose ester such as cellulose acetate hydrolyzed to an acetyl content of 19 to 26% as described in US. Patent 2,327,808 of Lowe and Clark, issued Aug.
  • cyano-acetyl groups such as the vinyl alcohol-vinyl cyanoacetate copolymer as described in Unruh, Smith and Priest, US. Patent 2,808,331, issued Oct. 1, 1957; or a polymeric material which results from polymerizing a protein or a saturated acrylated protein with a monomer having a vinyl group as described in Illingsworth, Dann and Gates, US. Patent 2,852,382, issued Sept. 19, 1958.
  • the silver halide emulsions of my invention can be spectrally sensitized with cyanine and merocyanine dyes, such as those described in Brooker, US. Patents 1,846,- 301 (issued Feb. 23, 1932), 1,846,302 (issued Feb. 23, 1932), and 1,942,854 (issued Jan. 9, 1934); White, U.S. Patent 1,990,507 (issued Feb. 12, 1935); Brooker and White, US. Patents 2,112,140 (issued Mar. 22, 1938), 2,165,338 (issued July 11, 1939), 2,493,747 (issued Jan. 10, 1950), and 2,739,964 (issued Mar. 27, 1956); Brooker and Keyes, US. Patent 2,493,748 (issued Jan.
  • the silver halide emulsions of the invention can also contain any of the conventional addenda of light-developable, direct-print emulsions such as gelatin plasticizers, hardeners, coating aids and the like.
  • Typical supports for photographic elements of the invention include glass, metals, paper, polyethylene-coated paper, polypropylene-coated paper, cellulose nitrate film, cellulose acetate film, polycarbonate film, polyvinyl acetal film, polystyrene film, polyethyleneterephthalate film and related films of resinous materials and others.
  • the photographic element is initially exposed to a relatively short duration and high intensity source of electromagnetic radiation (e.g., at least about .1 footcandle second at an intensity of more than about 100 foot-candles) such as a high intensity light source such as are used in oscillographs described in Heiland, US. Patent 2,580,427, issued Jan. 1, 1952, high intensity visible light, x-radiation and the like, to form a latent image in the emulsion of the photographic element.
  • a relatively short duration and high intensity source of electromagnetic radiation e.g., at least about .1 footcandle second at an intensity of more than about 100 foot-candles
  • a high intensity light source such as are used in oscillographs described in Heiland, US. Patent 2,580,427, issued Jan. 1, 1952, high intensity visible light, x-radiation and the like
  • Typical suitable high-intensity light sources are mercury vapor lamps that have high blue and ultraviolet emission, xenon lamps that emit light of wavelengths similar to daylight, and tungsten lamps that have high red light emission.
  • the resulting latent image is photodeveloped by overall exposure of the emulsion to a radiation source (e.g., at least about .0001 foot-candle second) of lower intensity than the original exposure, such as to a conventional fluorescent light, light from incandescent lamps commonly used for general illumination, or even ordinary daylight.
  • a radiation source e.g., at least about .0001 foot-candle second
  • the latent image formed in the emulsion in the first instance is not visible and does not become visible until photodevelopment.
  • Heat is desirably utilized during the photodevelopment step.
  • the subject emulsions are heated to a temperature of about 6 C. to 200 C. for about 1 to 30 seconds and photodeveloped after the initial high intensity exposure.
  • photographic elements containing the emulsions of the invention can be developed and fixed in aqueous chemical developing-out and fixing solutions after the initial exposure forming the latent image, or after the above-described photodevelopment, to make archivalquality records.
  • Developing agents can be incorporated in the emulsions of the invention including such developing agents as hydroquinones, catechols, amino-phenols, 3-pyrazolidones and the like.
  • Photographic elements having the light-developable, direct-print silver halide emulsions coated thereon are particularly characterized in possessing a combination of properties desired of such materials, particularly, relatively high speed, resistance to image fading and good chemical development characteristics.
  • Photodeveloped images can be conveniently overcoated with such filter materials by means of an aerosol spray comprising a fast drying dyed lacquer (eg, a cellulose lacquer) which does not transmit substantial light in the spectral region causing photochemical action in the underlyin silver halide emulsion.
  • photographic elements containing the emulsions of the invention can contain an overcoated mordant layer, and a photodeveloped image in such emulsions inhibited from fading 'by bathing the photographic image in a solution of a suitable mordantable dye such as C. 1. Acid Yellow 1, C, I. Acid Yellow 23, C. I. Direct Yellow 50, C. I. Acid Yellow 27, C. 1. Acid Yellow 17 and the like.
  • EXAMPLE 1 A series of light-developable, direct-print, light-sensitive gelatino silver chlorobromide (5 mole percent chloride and mole percent bromide) emulsions were prepared by slowly adding an aqueous solution of silver nitrate containing 0.85 g. of lead nitrate per mole of silver nitrate and a solution of potassium bromide and sodium chloride to an agitated 1.1% aqueous gelatin solution at 60 C. with the pH adjusted to about 2.0 with nitric acid.
  • Various addenda were added to be present during the precipitation oft he silver halide in the preparation of the various emulsions as summarized below in Table A. The concentrations of the respective addenda are indicated in Table A in terms of grams per mole of silver halide,
  • each of the prepared emulsions was added about .4 mole percent based on the silver halide of a thiourea halogen acceptor, and about 2 mole percent based on the silver halide of potassium iodide.
  • Each of the emulsions was also spectrally sensitized with a thiazoline-thiohydantoin merocyanine dye as described in copending Jones application Ser. No. 380,044 filed July 2, 1964.
  • the emulsions were then coated on a photographic paper support at a silver coverage of 260 mg. per square foot and at a gelatin coverage of 480 mg. per square foot.
  • the coatings were exposed through a 0.15 log E neutral density step wedge for 10 seconds in an EG&G Mark VI sensitometer.
  • the resulting latent images in the coated emulsions were photo-developed with an overall exposure to daylight fluorescent illumination for minutes, 35 footcandles. Maximum and minimum density readings were observed as well as the number of visible 0.15 log E steps.
  • the maximum densities (D are the densities in the areas of exposure and the minimum densities (D are the densities in background or nonimage areas,
  • the number of visible 0.15 log E steps is an indication of the photographic speed of the respective emulsions.
  • the resulting photodeveloped coatings were then subjected for 63 hours to 70 foot-candles of daylight fluorescent light and D D and number of 0.15 density steps observed to measure print permanence of the images. The results are summarized by the data set out in Table B below.
  • the photographic emulsions of the invention can also be chemically developed after imagewise exposure and photo-development if such is desired to make archival quality records.
  • a photographic element having coated thereon Emulsion A described in Example 1 was exposed and photodeveloped as described in Example 1.
  • the resulting photographic element was chemically developed in Kodak D-72 developer for 60 seconds at 70- F., and thereafter fixed in hypo, washed and dried in the usual manner.
  • the original D areas of the photodeveloped emulsion did not chemically develop to a substantial density while the original D areas of the photodeveloped emulsion did chemically develop to a high density. A reversal image was obtained.
  • the present invention thus provides a new and useful class of light-developable, direct-print silver halide emulsions.
  • Such emulsions are particularly characterized as possessing a combination of properties highly desirable in the present field, including high photodeveloped image discrimination, high print permanence, high sensitivity, and good chemical processing capability.
  • the present emulsions have high sensitivity for both high speed and low speed recording.
  • r is an integer of 1 to 3.
  • the improvement which comprises forming the grains of said silver halide in an acidic media in the presence of a water-soluble thiocyanate and an organic thioether silver halide solvent, an aqueous solution of said thioether at a 0.02 molar concentration being capable of dissolving more than twice the amount of silver chloride than that which can be dissolved by water at C.

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  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
US507233A 1965-11-10 1965-11-10 Light-developable direct-print silver halide emulsions Expired - Lifetime US3507657A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3957490A (en) * 1973-04-26 1976-05-18 Agfa-Gevaert N.V. Method of preparing photographic silver halide emulsions
US4695535A (en) * 1986-12-29 1987-09-22 Eastman Kodak Company Silver halide photosensitive material
US5252455A (en) * 1992-03-04 1993-10-12 Eastman Kodak Company Photographic silver halide material comprising gold (I) complexes comprising sulfur- and/or selenium-substituted macrocyclic polyether ligands

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3260605A (en) * 1962-01-05 1966-07-12 Eastman Kodak Co Method for preparing light-sensitive silver halide emulsions suitable for print-out recording materials
US3271157A (en) * 1962-09-11 1966-09-06 Eastman Kodak Co Light-developable direct-print silver halide emulsions

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1368647A (fr) * 1962-09-11 1964-07-31 Kodak Pathe Nouvelle émulsion photodéveloppable

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3260605A (en) * 1962-01-05 1966-07-12 Eastman Kodak Co Method for preparing light-sensitive silver halide emulsions suitable for print-out recording materials
US3271157A (en) * 1962-09-11 1966-09-06 Eastman Kodak Co Light-developable direct-print silver halide emulsions

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3957490A (en) * 1973-04-26 1976-05-18 Agfa-Gevaert N.V. Method of preparing photographic silver halide emulsions
US4695535A (en) * 1986-12-29 1987-09-22 Eastman Kodak Company Silver halide photosensitive material
US5252455A (en) * 1992-03-04 1993-10-12 Eastman Kodak Company Photographic silver halide material comprising gold (I) complexes comprising sulfur- and/or selenium-substituted macrocyclic polyether ligands
US5391727A (en) * 1992-03-04 1995-02-21 Eastman Kodak Company Photographic silver halide material comprising novel gold compound

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BE689515A (enrdf_load_stackoverflow) 1967-04-14
GB1166074A (en) 1969-10-01

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