US3201242A - Accelerators for reversal color development - Google Patents

Accelerators for reversal color development Download PDF

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US3201242A
US3201242A US137041A US13704161A US3201242A US 3201242 A US3201242 A US 3201242A US 137041 A US137041 A US 137041A US 13704161 A US13704161 A US 13704161A US 3201242 A US3201242 A US 3201242A
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color
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dithia
photographic
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US137041A
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Judith A Schwan
John R Dann
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Eastman Kodak Co
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Eastman Kodak Co
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Priority to US137041A priority patent/US3201242A/en
Priority to DEE23468A priority patent/DE1147845B/en
Priority to FR908771A priority patent/FR1351410A/en
Priority to GB22017/65A priority patent/GB1020033A/en
Priority to GB34357/62A priority patent/GB1020032A/en
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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
    • G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
    • G03C7/407—Development processes or agents therefor
    • G03C7/413—Developers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/145—Infrared
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/167—X-ray

Definitions

  • This invention relates to color photography, and more particularly, to a method of processing multi-layer color films or papers by the technique of reversal color development.
  • multi-layer photographic elements used for color photography there are generally three selectively sensitive emulsion layers (each of which may consist of several strata finished to different speed levels) coated on the same side of a photographic support, such as film or paper.
  • a photographic support such as film or paper.
  • the uppermost layer is frequently a blue-sensitive layer
  • the next light-sensitive layer is generally green-sensitive
  • the light-sensitive layer closest to the support is generally sensitized to the red region of the spectrum.
  • photographic elements inasmuch as many photographic silver halide emulsions have substantial inherent sensitivity in the blue spectral region, such photographic elements generally have a yellow filter layer coated beneath the blue-sensitive outermost layer for the purpose of absorbing substantially all blue radiation which would otherwise be transmitted to the green-sensitized and redsensitized layers.
  • Such multi-layer photographic elements can also have other layers for specialized purposes including light sensitive emulsion layers, gelatin or other subbing layers, antihalation layers, etc.
  • Typical multilayer photographic materials useful in our invention have been described in the prior art, such as Mannes et al. US. Patent 2,252,718, issued August 19, 1951.
  • Color materials of the type advantageously employed in the present invention are those intended primarily for reversal color processes, in which the photoexposed material is given a conventional black-and-white development to produce a negative silver image but no color image, followed by at least one reversal re-exposure and color development to produce positive dye (and silver) images.
  • the color materials used in our invention comprise those which contain the color-forming materials or couplers within the silver halide emulsions, or those materials designed for processing in developers which contain the color couplers or color-forming compounds within the color developer. The latter materials are particularly useful in practicing the present invention for reasons pointed out below.
  • an object of our invention to provide an improved process for producing photographic images in color by reversal color photography. Another object is to provide improved developers for such reversal color photographic processes. Still another object is to provide a method of increasing the color density in certain of the emulsion layers of photographic color elements, particularly in the red-sensitive of cyan-producing layer. Still another object is to provide a convenient means for avoiding re-eXposure by light, by simultaneously fogging and color developing photographic silver halide emulsion to produce a colored image of high maximum density. Other objects will become apparent from a consideration of the following description and examples.
  • the conventional procedure is to selectively re-expose with colored light (or chemicals) each of the selectively sensitized layers and to separately develop each of these layers to a colored image in a color developer which contains the appropriate color-forming ingredient in the color developer.
  • color processes of this type it is frequently desired to accelerate color development so that the rate of development is increased without fogging the silver halide grains which have not been exposed by the selective exposure.
  • Such accelerators increase the maximum color density with little or no increase in color fog.
  • the compounds of our invention can be used to increase the development rate of multi-layer photographic materials which are processed in developing solutions containing the color-forming components in the color developing solutions so that substantially all silver halide, which has been selectively re-exposed to a particular region of the spectrum, becomes developed in the subsequent color developing solution, thus preventing the formation of undesirable color fog as a consquence of further color development in a subsequent color developer for producing different colored images.
  • thioether compounds useful in practicing our invention by incorporation in the color developer comprise compounds represented by the following general formula:
  • X represents a divalent linkage, such as oxygen, sulfur,
  • R represents a hydroxyl group, an allcoxyl group (e.g.,' methoxyl, ethoxyl, propoxyl, butoxyl, etc), a carbamyl group (i.e., an aminocarbonyl group), or a carboxylic acyloxyl group, such as acetoxyl, bntyroxyl, etc.
  • R represents an ethylene radical, such as ethylene or ethylene Cs substituted by an alkyl radical, such as methyl, ethyl, etc, represents a positive integer of from 1 to 2 and n represents a positive integer of from 1 to 3.
  • R and R each represents an 'alky'lene group, such as ethylene, trimethylene, tetramethylene (butylene), methyl-substituted trimethylene, pentamethylene, ethyl-substituted tetramethylene, hexamethylene, 'heptamethylene, octa'methylene, nonamethylene, decamethylene, et-c. (e.g., a hydrocarbon alkylene group containing from about 2 to 11) carbon atoms), and d represents a positive integer of from 1 to 3.
  • dithiaalkylencd-iols such as those embraced by the following general formula:
  • n each represents a positive integer of from about 2 to 10.
  • the concentration of the thioether compound in the color developer is at least 0.1 gram per liter. Larger amounts of-thioether compounds can be employed in the color developers, and concentrations as high as 5 grams (or higher) per liter are useful.
  • the activity of the color developers will obviously depend upon the development temperature, duration of development and the like. All of these variables are Well understood by those skilled in the art of photography.
  • the most advantageous concentration for a particular developer can be determined by developing a series of test strips of silver halide emulsions wherein the concentration of thioether compound is varied.
  • the color developers useful in our invention can also contain conventional addenda, such as alkaline salts (e.g., sodium carbonate, potassium carbonate, sodium hydroxide, sodium, metaborate, etc.), restraining agents, such as potassium bromide, stain preventives, such as alkali metal sulfites, etc. i
  • photographic emulsions used in practicing our invention are of the developing-out type.
  • the emulsions can be chemically sensitized by any of the accepted procedures.
  • the emulsions can be digested with naturally active gelatin, or sulfur compounds can be added such as those described in Sheppard US. Patent 1,574,944, issued March 2, 1926, Sheppard et al. US. Patent 1,623,499, issued April 5, 1927, and Sheppard et al. US. Patent 2,410,689, issued November 5, 1946.
  • the emulsions can also be treated with salts of the noble metals such as ruthenium, rhodium, palladium, iridium, and platinum.
  • the noble metals such as ruthenium, rhodium, palladium, iridium, and platinum.
  • Representative compounds are ammonium chloropalladate, potassium chloroplatinate, and
  • sodium chloropall'adite which are used for sensitizing in amounts below that which produces any substantial fog inhibition, as described in Smith and Trivelli U.S. Patent 2,448,060, issued August 31, 1948, and as antifoggants in higher amounts, as described in Trivelli and Smith US. Patents 2,566,245, issued August 28, 1951, and 2,566,263, issued August 28, 1951.
  • the emulsions can also be chemically sensitized with gold salts as described in Waller et al. US. Patent 2,399,- 083, issued April 23, 1946, and Damschroder et al. US. Patent 2,642,361, issued June 16, 1953.
  • Suitable compounds are potassium chloroaurite, potassium aurithiocyanate, potassium chloroaurate, auric trichloride and 2- aurosulfobenzothiazole methochloride.
  • the emulsions can also be chemically sensitized with reducing agents such as stannous salts (Carroll U.S. Patent 2,487,850, issued November 15, 1949), polyamines, such as diethylene triamine (Lowe and Jones US. Patent 2,518,698, issued August 15, 1950), polyamines, such as spermine (Lowe and Allen U.S. Patent 2,521,925, issued September 12, 1950), or bis(fl-amiuoethyl) sulfide and its Water-soluble salts (Lowe and Jones US. Patent 2,521,926, issued September 12, 1950).
  • reducing agents such as stannous salts (Carroll U.S. Patent 2,487,850, issued November 15, 1949), polyamines, such as diethylene triamine (Lowe and Jones US. Patent 2,518,698, issued August 15, 1950), polyamines, such as spermine (Lowe and Allen U.S. Patent 2,521,925, issued September 12, 1950), or bis(fl-amiuoethyl) s
  • the emulsions can also be optically sensitized with cyanine and merocyanine dyes, such as those described in Brooker US. Patents 1,846,301, issued February 23, 1932; 1,846,302, issued February 23, 1932; and 1,942,854, issued January 9, 1934; White US. Patent 1,990,507, issued February 12, 1935; Brooker and White US. Patents 2,112,140, issued March 22, 1938; 2,165,338, issued July 11, 1939; 2,493,747 issued January 10, 1950, and 2,739,964, issued March 27, 1956; Brooker and Keyes US. Patent 2,493,748, issued January 10, 1950; Sprague US.
  • cyanine and merocyanine dyes such as those described in Brooker US. Patents 1,846,301, issued February 23, 1932; 1,846,302, issued February 23, 1932; and 1,942,854, issued January 9, 1934; White US. Patent 1,990,507, issued February 12, 1935; Brooker and White US. Patents 2,112,140, issued March 22, 1938; 2,165
  • the emulsions can also be stabilized with the mercury compounds of Allen, Byers and Murray U.S. Patent 2,728,663, issued December 27, 1955; Carroll and Murray US. Patent 2,728,664, issued December 27, 1955; and Leubner and Murray US. Patent 2,728,665, issued December 27, 1955; or with gold salts as described in Damschroder US. Patent 2,597,856, issued May 27, 1952,
  • the emulsions may also contain speed increasing com- 7 pounds of the quaternary ammonium type of Carroll U.S. Patent 2,271,623, issued February 3, 1942; Carroll and Allen U.S. Patent 2,288,226, issued June 30, 1942; and Carroll and Spence U.S. Patent 2,334,864, issued November 23, 1943; or the polyethylene. glycol type of Carroll and Beach U.S. Patent 2,708,162, issued May 10,195; or the quaternary ammonium salts and polyethylene glycols of Piper U.S. Patent 2,886,437, issued May 12,
  • T he emulsions may contain .a suitable gelatin plasticizer such as glycerin; a dihydroxy alkane such as 1,5-pentane diol as described in Milton and Murray U.S. application Serial No. 588,951, filed June 4, 1956 (now U.S. Patent 2,960,404, issued November 15, 1960); an ester of an ethylene bis-glycolic acid such as ethylene bis(methyl glycolate) as described in Milton U.S. Patent 2,904,434, issued September 15, 1959; bis-(ethoxy diethylene glycol) succinate as described in Gray U.S. application Serial No. 604,333, filed August 16, 1956 (now U.S.
  • the plasticizer may be added to the emulsion before or after the addition of a sensitizing dye, if used.
  • the emulsions may be hardened with any suitable hardener for gelatin such as formaldehyde; a halogen-substituted aliphatic acid such as mucobromic acid as described in White U.S. Patent 2,080,019, issued May 11, 1937; a compound having a plurality of acid anhydride groups such as 7,8-diphenylbicyclo(2,2,2) 7 octene- 2,3,5,6-tetra-carboxylic dianhydride, or a dica'rboxylic or adisulfonic acid chloride such as terephthaloylchloride as described in Allen and Carroll U.S.
  • any suitable hardener for gelatin such as formaldehyde
  • a halogen-substituted aliphatic acid such as mucobromic acid as described in White U.S. Patent 2,080,019, issued May 11, 1937
  • a compound having a plurality of acid anhydride groups such as 7,8-diphen
  • Patent 2,950,197 issued August 23, 1960
  • 2,3-dihydroxy dioxane as described in JelTreys
  • bisisocyanate as described in Henn et a1.
  • the emulsions may contain a coating aid such as saponin; a 'lauryl or oleyl monoether of polyethylene glycol as described in Knox and Davis U.S. Patent 2,831,766, issued April 22, 1958; a salt of a sultated and alkylated polyethylene glycol ether as described in Knox and Davis U.S. Patent 2,719,087, issued September 27, 1955; an acylated alkyl taurine such as the sodium salt of N-oleoyl-N-methyl taurine as described in Knox, Twardokus and Davis U.S.
  • a coating aid such as saponin
  • a 'lauryl or oleyl monoether of polyethylene glycol as described in Knox and Davis U.S. Patent 2,831,766, issued April 22, 1958
  • a salt of a sultated and alkylated polyethylene glycol ether as described in Knox and Davis U.S. Patent 2,719,087, issued September 27, 1955
  • Patent 2,739,891 issued March 27, 1956; the reaction product of a dianhydride of tetracar-- boxybutane with an alcohol or an aliphatic amine containing from 8 to 18 carbon atoms which is treated with a base, for example, the sodium salt of the monoester of tetracarboxybutane as described in Knox, Stenberg and Wilson U.S. Patent 2,843,487, issued July 15, 1958; a water-soluble maleopimarate as described in Knox and Fowler U.S. Patent 2,823,123, issued February 11, 1958; an alkali metal salt of a substituted amino acid such as disodium N-(carbo p tert.
  • a base for example, the sodium salt of the monoester of tetracarboxybutane as described in Knox, Stenberg and Wilson U.S. Patent 2,843,487, issued July 15, 1958; a water-soluble maleopimarate as described in Knox and Fowler U.S. Patent 2,823,123, issued February
  • the addenda which we have described may be used in various kinds of photographic emulsions. In addition to being useful in X-ray and other nonoptically sensitized emulsions they may also be used in orthochromatic, panchromatic, and infrared sensitive emulsions. They may be added to the emulsion before or after any sensitizing dyes which are used.
  • Various silver salts may be used as the sensitive salt such assilver bromide, silver iodide, silver chloride, or mixed silver halides such as silver chlorobromide or silver bromoiodide.
  • the agents maybe used in emulsions intended for color photography, for example, emulsions containing color-forming couplers or emulsions to be developed by solutions containing couplers or other color-generating materials, emulsions of the mixed-packet type, such as described in Godowsky U.S. Patent 2,698,794, issued January 4, 1955; or emulsions of the mixed-grain type, such as described in Carroll and Hanson U.S. Patent 2,592,243, issued April 8, 1952.
  • These agents can also be used in emulsions which form latent images predominantly on the surface of the silver halide crystal or in emulsions which form latent images predominantly inside the silver halide crystal, such as those described in Davey and Knott U.S. Patent 2,592,250, issued Apr-i1 8; 1952.
  • the dispersing agent for the silver halide in its preparation gelatin or some other colloidal material such as colloidal albumin, a cellulose derivative or a synthetic resin, for instance, a poyvinyl compound.
  • colloidal albumin a colloidal albumin
  • a cellulose derivative a synthetic resin
  • poyvinyl compound a colloidal compound which may 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,
  • Patent 2,768,154 issued October 23, 1956; or containing,
  • cyano-acetyl groups such as the vinyl alcohol-vinyl cyanoacetate copolymer as described in Unruh, Smith and Priest US. Patent 2,888,331, issued October 1, 1957; or a polymeric material which results from polymerizing a protein or a saturated acylated protein with a monomer having a vinyl group as described in Us. Patent 2,852,382, of Illingsworth, Dann and Gates, issued September 16, 1958.
  • compatible mixtures of two or more of these colloids may be employed for dispersing the silver halide in its preparation.
  • Combinations of these antifoggants, sensitizers, hardeners, etc., may be used.
  • Couplers or color-forming compounds which are soluble in the strongly alkaline developing solutions are well known to those skilled in the art.
  • Typical couplers include the following:
  • amylbenzenesulfonylamino) -5- pyrazolone (37) 1-phenyl-3-[p-(p-sec. amylbenzoyl) aminobenzoylamino]-5-pyrazolone (3 8) 1-m-tolyl-3-[m-(fi-phenylpropionyl) aminobenzoylamino] -5-pyrazolone (39) 1-m-tolyl-3-(2,4-di-tert.butyl-mtolyloxyacetylamino) -5-pyrazolone (40) 1-[p'-(p-tert.
  • amylphenoxyacetanilide (77) benzoylacetamido-3-methoxy-2,4'-di-tert.-
  • Couplers suitable for use in the emulsions of our invention comprise those disclosed in Spence and Carroll US. Patent 2,640,776, issued June 2, 1953, Weissberger et al. US. Patent 2,407,210, issued September 3, 1946, and Weissberger et al. US. Patent 2,474,293,
  • the color-forming developers useful in our invention have been previously described in the prior art, and our invention is not to be restricted to the use of any particular color-forming developer.
  • the color-forming developers previously mentioned which we have found to be especially useful in our invention. comprise aromatic primary amines containing an amino (substituted or not) or hydroxyl substituent. Phenylenediamines and substituted derivatives thereof containing a primary amino group have been found to provide excellent results when employed in combination with the formamidinothiomethyl compounds of our invention.
  • Typical of such color-forming developers are the sulfonamido substituted p-phenylenediamines disclosed in Weissberger US. Patent 2,548,574, issued April 10,
  • the first developer employed in the process of our invention is generally a rapid developer of the MO type
  • filter i.e., a filter transmitting only visible radiation beyond about 620 III/.1. with maximum transmittance of about 88 percent at 700 mu.
  • Each of the strips was developed for ten minutes at 80 F. in a cyan developer having the composition given below.
  • One of the film strips served as a control and contained no thioether compound, while the other strips were developed in cyan developers containing thioether compounds in amounts identified in the following table.
  • the compound numbers in the table correspond to the compound numbers given above for the thioether compounds.
  • the cyan developer which served as a control and to which the thioether compounds were added had the following formula:
  • a multi-layer color film of the type used in Example 1 was cut into several strips and each of these exposed for second to a SOD-watt 3000 K. light source on an Eastman Type Ib Sensitometer. Each of the strips was then developed for nine minutes at 80 F. to a black-andwhite negative developer of the type described in the above example and washed for five minutes in 80 F. water. Strips were then treated in an antifoggant bath of the type described in the above example for two minutes at 80 F. and washed for two minutes in 80 F.
  • R represents a member selected from the class consisting of a hydroxyl group, an alkoxyl group, and a carbamyl group
  • R represents an ethylene radical
  • X represents a divalent radical selected from the class consisting of an oxygen atom, a sulfur atom and the group X CH CH X X and X each represents a divalent radical selected from, the class consisting of an oxygen atom and a sulfur atom, provided at least one of the radicals selected from the class consisting of X, X and X represents a sulfur atom
  • X represents the divalent radical d represents a positive whole number of from 1 to 2 and n represents a positive whole number of from 1 to 3.
  • a photographic color developer comprising an aquous alkaline solution of a p-phenylenediamine color developing agent, a color-forming compound capable of coupling with the oxidation products of said color developing agent to provide a colored image, and a non-pol l V ymeric compound selected from those represented by the following general formula:
  • R represents a member selected from the class consisting of a hydroxyl group, an alkoxyl group, and a carbamyl group
  • R represents an ethylene radical
  • X represents a divalent radical selected from the class consisting of an oxygen atom, a sulfur atom
  • X CH CH X1, X and X each represents a divalent radical selected from the class consisting of an oxygen atom and a sulfur atom, provided at least one of the radicals selected from the class consistmg of X, X and X represents a sulfur atom, X represents the divalent radical wherein R represents a member selected from the class consisting of a hydroxyl group, an alkoxyl group and a carbamyl group, X represents a divalent radical selected from the class consisting of an oxygen atom, a sulfur atom,
  • a photographic color developer comprising an aqueous alkaline solution, of a p-phenylenediamine color developing agent, a phenolic compound capable of coupling with the oxidation products of said color developing agent to provide a cyan photographic image, and a nonpolymeric compound selected from those represented by the following general formula:
  • R represents a member selected from the class consisting of a hydroxyl group, an :alkoxyl group, and a caroamyl group
  • R represents an ethylene radical
  • X represents a divalent radical selected from the class con- 'sisting of an oxygen atom, a sulfur atom
  • NHCI-I2NHC- and the radical X CH CH X X and X each represents a divalent radical selected from the class consisting of an oxygen atom and a sulfur atom, provided at least one of the radicals selected from the class consisting of X, X and X represents a sulfur atom, and n represents a positive whole number of from 1 to 3.
  • a photographic color developer comprising an aqueous alkalinesolution of a p-phenylenediamine color developing agent, a compound capable of coupling with the oxidation products of said color developing agent to produce a colored photographic image, and a non-polymeric compound selected from those represented by the following general formula:
  • R and R each represents a hydrocarbon alkylene group containing from about 2 to 10 carbon atoms and d represents a positive integer of from 1 to 3.
  • a photographic color developer comprising an aqueous alkaline solution of a p-phenylenediamine color de veloping agent, a compound capable of coupling with'the oxidation products of said color developing agent to produce a colored photographic image, and a non-polymeric compound selected from those represented by the following general formulai wherein m and it each represents a positive integer of from about 2 to 10.
  • a photographic color developer comprising an aqueous alkaline solution of a p-phenylenediamine color developing agent, a pyrazolone compound capable of coupling with the oxidation products of said color developing agent to produce a magenta photographic image and a non-polymeric sompound selected from those represented by the following general formula:
  • R and R each represents a hydrocarbon alkylene group containing from about 2 to 10 carbon atoms and d represents a positive integer of from 1 to 3.
  • a photographic color developer comprising an aqueous alkaline solution of an arylenediamine color developer and the compound having the formula:
  • a photographic color developer comprising an aqueous alkaline solution of an arylenediamine color developer and the compound having the formula:
  • a photographic color developer comprising an aqueous alkaline solution of an arylenediamine color developer and'the compound having'the formula:
  • a photographic color developer comprising an aqueous alkaline solution of an arylenediamine color deveioper and the compound having the formula:
  • a photographic color developer comprising an aqueous alkaline solution of an arylenediamine color de veloper and the compound having the formula:

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Description

United States Patent 3,2lll,242 accurnnarons t on nnvnnsar. coLon DEVELQP'MENT I ,ludith A. Schwan and .lohn R. Darin, both of Rochester,
This invention relates to color photography, and more particularly, to a method of processing multi-layer color films or papers by the technique of reversal color development.
In multi-layer photographic elements used for color photography, there are generally three selectively sensitive emulsion layers (each of which may consist of several strata finished to different speed levels) coated on the same side of a photographic support, such as film or paper. For example, the uppermost layer is frequently a blue-sensitive layer, the next light-sensitive layer is generally green-sensitive and the light-sensitive layer closest to the support is generally sensitized to the red region of the spectrum. inasmuch as many photographic silver halide emulsions have substantial inherent sensitivity in the blue spectral region, such photographic elements generally have a yellow filter layer coated beneath the blue-sensitive outermost layer for the purpose of absorbing substantially all blue radiation which would otherwise be transmitted to the green-sensitized and redsensitized layers. Such multi-layer photographic elements can also have other layers for specialized purposes including light sensitive emulsion layers, gelatin or other subbing layers, antihalation layers, etc. Typical multilayer photographic materials useful in our invention have been described in the prior art, such as Mannes et al. US. Patent 2,252,718, issued August 19, 1951.
Color materials of the type advantageously employed in the present invention are those intended primarily for reversal color processes, in which the photoexposed material is given a conventional black-and-white development to produce a negative silver image but no color image, followed by at least one reversal re-exposure and color development to produce positive dye (and silver) images. The color materials used in our invention comprise those which contain the color-forming materials or couplers within the silver halide emulsions, or those materials designed for processing in developers which contain the color couplers or color-forming compounds within the color developer. The latter materials are particularly useful in practicing the present invention for reasons pointed out below.
It is, therefore, an object of our invention to provide an improved process for producing photographic images in color by reversal color photography. Another object is to provide improved developers for such reversal color photographic processes. Still another object is to provide a method of increasing the color density in certain of the emulsion layers of photographic color elements, particularly in the red-sensitive of cyan-producing layer. Still another object is to provide a convenient means for avoiding re-eXposure by light, by simultaneously fogging and color developing photographic silver halide emulsion to produce a colored image of high maximum density. Other objects will become apparent from a consideration of the following description and examples.
in the processing of photographic multi-layer materials by the reversal technique using color couplers in the developing compositions rather than in the emulsion layers, the conventional procedure is to selectively re-expose with colored light (or chemicals) each of the selectively sensitized layers and to separately develop each of these layers to a colored image in a color developer which contains the appropriate color-forming ingredient in the color developer. In color processes of this type, it is frequently desired to accelerate color development so that the rate of development is increased without fogging the silver halide grains which have not been exposed by the selective exposure. Such accelerators increase the maximum color density with little or no increase in color fog.
In the processing of multi-layer photographic elements to produce a colored image, it is sometimes desired to have a color development bath which results in development of all silver halide remaining in the respective layers and to couple the color-forming compound with the oxidation products of the appropriate color developer to produce dye images in the respective photographic silver halide emulsion layers. Such results are desired principally in photographic multi-layer materials which contain the color-forming component or coupler within the silver halide emulsion layers, or in the final color development step in a color process in which the color formin" component is incorporated within the color developing solution.
We have now found that the afore-mentioned effects can be advantageously attained by incorporating certain non-polymeric, thioether compounds in color developers intended for use in reversal color development. The compounds of our invention can be used to increase the development rate of multi-layer photographic materials which are processed in developing solutions containing the color-forming components in the color developing solutions so that substantially all silver halide, which has been selectively re-exposed to a particular region of the spectrum, becomes developed in the subsequent color developing solution, thus preventing the formation of undesirable color fog as a consquence of further color development in a subsequent color developer for producing different colored images. Thus, it is possible to prevent the formation of cyan dye in the greenand bluesensitive layers of such multi-layer color elements and to form cyan dye substantially only in the red-sensitive layer. It is also possible according to our invention to render substantially all residual silver halide in such multi layer photographic elements developable by incorporating such thioether compounds in the color developers.
The thioether compounds useful in practicing our invention by incorporation in the color developer (or color developers) comprise compounds represented by the following general formula:
wherein X represents a divalent linkage, such as oxygen, sulfur,
R represents a hydroxyl group, an allcoxyl group (e.g.,' methoxyl, ethoxyl, propoxyl, butoxyl, etc), a carbamyl group (i.e., an aminocarbonyl group), or a carboxylic acyloxyl group, such as acetoxyl, bntyroxyl, etc., R represents an ethylene radical, such as ethylene or ethylene Cs substituted by an alkyl radical, such as methyl, ethyl, etc, represents a positive integer of from 1 to 2 and n represents a positive integer of from 1 to 3.
The compounds of Formula I above can be prepared according to methods which have been previously described in the technical literature. Preparations for a number of compounds coming within the scope of this formula are described in Dann, Chiesa and Lovett, U.S.
application Serial No. 846,230, filed October 14, 1959.
Another group of compounds coming with the scope of Formula I above which can advantageously be employed in our invention comprise compounds represented by the following general formula:
I ll CHgO CHzCHzO (i1 CHgSCHzC H O CH CHZ O CHZCIIQSCHQC O CIIQCHZO CH wherein R and R each represents an 'alky'lene group, such as ethylene, trimethylene, tetramethylene (butylene), methyl-substituted trimethylene, pentamethylene, ethyl-substituted tetramethylene, hexamethylene, 'heptamethylene, octa'methylene, nonamethylene, decamethylene, et-c. (e.g., a hydrocarbon alkylene group containing from about 2 to 11) carbon atoms), and d represents a positive integer of from 1 to 3. Especially useful sensitizing compounds, according to our invention, are dithiaalkylencd-iols, such as those embraced by the following general formula:
wherein m and n each represents a positive integer of from about 2 to 10.
Compounds represented by Formulas H and III above can be prepared according to methods which have been previously described in the technical literature. The preparation'having a number of such compounds i given in Williams and (lesser U.S. application Serial No. 843,- 638, filed October 1, 1959 (now US. Patent 3,021,215, issued February 13, 1962).
Typical compounds useful in our invention embraced by the above general formulas include the following:
( 1) HOCH CH SCH CI EOCH 01-1 0 CH CH SCH CH OI-1 1,14-dihydroxy-6,9-dioxa-3,IQ-dithiatetradecane CH CH O CH CH OCH CH SCH CH 3,6,12,18,21-pentoXa-9,1S-dithiatricosane C H OCH -CH OCH CH SCH CH OCH CH O C H 3,6,12,15-tetraoxa-lO-thiaheptadecane CH OCH CH SCH CH OCH CH OCH CH SCH CH OCH 2,8,1 1,17-tetroxa-5,14-dithiaoctadecane CH CH OCH CH OCH CH OCH CH SCH OH OCH C'H OCH CH OCH CH 3 ,6,9,15,18,2-1-hexoxadZ-thiatricosane CH CH OCH CH SCH CH OCH CH OCH CH SCH CH O CH CH 3 ,9,12,184tetroxa 6, 15-dithiaeicosane CI1' CH OCH CH SCH CI-1 OCI-I CH SCH CH G CH CH 3 ,9, 15-trioxa-6,12-dithiaheptadecane CH CH O CH CH OOH OH SCH CH SCH CH OCH CH OCH CH 3,6,15,1'8-tetroXa-9,1Z-dithiaeicosane qOCH CH O O'CCH SCH C H OCH CH SCH COOCH CH OH 1,17-dihydroxy-3 ,9, 1 5-trioxa-6, l2- dithiaheptadeeane-4,l 4-dione 1 l HOCH CH GOCCH SCH CH OCH C11 0CH CH SCH COOCH OH OH 1,20-dihydroxy-3,9,12,l8-tetroxa-6,15-
dithiaeicosanel,17-dione 7,10-dioxa-4,13-dithiaheXadecane-Z,1S-dicarboxamide 2,5,11,14,20,23-hexoxa-8,17-dithiatetracosane-6,l9-dione i i. C1130 CHzCHzO C H23 CHzCHzO CHzCHzSCHzG O CHzCI-IzOO H 2,5,1 1, 17,20-pentoXa-8,14-dithiaheneicorsane-6,l6-dione 2)z t zh l zh "1,8-dihydroxy-3,6-dithiaoctane' (16) HO(CH S(OH S(CH OH 4,7-dithia1,10-decanediol (17) HO(CH S(CH S-(CH 0H 5,8-dithia-1,12-dodecanediol (18) HO(CH S(CH S(CH 0H 6,9-dithia1,4-tetradecanediol (19) HOKC'HQ S(CH 80C11 0H 7,10-dit hia-1,16-hexadecanediol (20) HO:(CH S(CH S(CH OH 10,13-dithia-1,22-docosanediol HO(CH2) 10 z)2 z)m 1 1,14-dithia- 1 ,24-tetracosanediol 3 ,7-dithia-1,9-nonanediol (23) HG (CH S(CH S=(CH GH 4,8-dithia-1,1l-undecanediol W M 2)3 (H2)4 5,9-dithia-l,13-tridecanediol (25) HO(CH S(CH S(CH) 0H 6,10-dithia-1,15-pentadecanediol (26) HO(CH S(CH S(CH OH 7,1l-dithia-1,17-heptadecanediol (27) HO(CH S(CH S(CH OH 10,14-dithia-1,2,3-tricosanedi0l HO(CH S(CH S(CH OH 1 1, 1S-dithia-1,25-pentacosanediol (29) HO(CH S(CH C(CI-I OH 3,8-dithia-1,10-decanedio1 (30) HO(CH S(CH S(CH 0H 4,9-dithia-1,12-dodecanediol (31) HO(CH S(CH S(CH OH 5,10-dithia-1, l4-tetradecanediol 2)5 2)4 2)5 6,1l-dithia-1,16-hexadecanediol (33) HO(CH S(CH S(H OH 7,12-dithia-1,l8-octadecanedio1 (34) HO(CH S(CH S(CH OH 10, 1S-dithia-1,24-tetracosanediol V I- 2)m 2)4 2)m 1 1,16-clithia-1,26-heXacosanediol (36) HO(CH S(CH S(CH OH 3,9-dithia-1,1l-undecanediol 2)3 2)5 2)3 4,10-dithia-1,13-tridecanediol s (38) HO(CH S(CH S(CH OH 6,12-dithia-1,17-heptadecanedio1 (39) HO(CH S(CH S(CH OH 7 ,13-dithia-1,19-nonadecanediol (40) HO(CH S(CH S(CH H 10,16-dithia-1,25-pentacosanediol (41) HO(CH S(CH S(CH 01-1 11,17-dithia-1,27-heptacosanediol (42) HO(CH S(CH S(CH OH 3, 1 O-dithia- 1 12-dodecanediol (43) HO(CH S(CH S(CH OH 4,1 l-dithia-l,14-tetradecanediol (44) HO(CH S (CH S(CH OH 5,12-dithia-1,16-hexadecanediol (45) H0(CH S(CH S(CH OH 6,13-dithia-1,18-octadecanediol (46) HO(CH S(CH S(CH OH 7,14-dithia-1,20-eicosanediol (47) HO(CH S(CH S(CH OI-l 10,17-dithia-1,26hexacosanediol 2)1o 2)e z)10 11,18-dithia-1,28-octacosanedi0l (49) HO(CH S(CH S(CH OH 3-13-dithia-1,1S-pentadecanediol (50) HO(CH S(CH) S(CH OH 4,14-dithia-1,17-heptadecanedio1 HO(CH2)4S(CH2)9S(CH2)40H 5,15-dithia-1,19-nonadecanediol (52) HO(CH S (CH S(CH OH 7,17-dithia-1,23-tricosanediol (53) HO(CH S(CH S(CH OH 10,20-dithia-1,29-nonacosanediol 2)l0 2)9 2)10 1 1,2 l-dithia- 1,3 l-hentriacoutanediol HO(CH2)2S(CH2)10S(CH2)2OH 3,14-dithia-1,16-hexadecanedio1 (56) HO(CH S(CH S(CH 0H 4,16-dithia-1,18-0ctadecanediol 2)4 2)10 2)4 5,16-dithia-1,20-eicosanediol 2)5 2)l0 2)5 6,17-dithia-1,22-docosanediol (59) HO(CH S(CH S(CH 0H 10,21-dithia-1,3 O-tricontanediol 2)1o 2)1o 2)10 1 1,22-dithia-1,32-dotriacontanedio1 The above thioether compounds useful in practicing our invention can be utilized in various concentrations,
depending upon the particular silverhalide emulsions employed, the thickness of the emulsion layers, the concentration of silver halides in the emulsions, the concentration of developing agents in the color developers, the pH of the color developers, etc. In general, We have found that useful results are obtained when the concentration of the thioether compound in the color developer is at least 0.1 gram per liter. Larger amounts of-thioether compounds can be employed in the color developers, and concentrations as high as 5 grams (or higher) per liter are useful. The activity of the color developers will obviously depend upon the development temperature, duration of development and the like. All of these variables are Well understood by those skilled in the art of photography. The most advantageous concentration for a particular developer can be determined by developing a series of test strips of silver halide emulsions wherein the concentration of thioether compound is varied. The color developers useful in our invention can also contain conventional addenda, such as alkaline salts (e.g., sodium carbonate, potassium carbonate, sodium hydroxide, sodium, metaborate, etc.), restraining agents, such as potassium bromide, stain preventives, such as alkali metal sulfites, etc. i
The photographic emulsions used in practicing our invention are of the developing-out type.
The emulsions can be chemically sensitized by any of the accepted procedures. The emulsions can be digested with naturally active gelatin, or sulfur compounds can be added such as those described in Sheppard US. Patent 1,574,944, issued March 2, 1926, Sheppard et al. US. Patent 1,623,499, issued April 5, 1927, and Sheppard et al. US. Patent 2,410,689, issued November 5, 1946.
The emulsions can also be treated with salts of the noble metals such as ruthenium, rhodium, palladium, iridium, and platinum. Representative compounds are ammonium chloropalladate, potassium chloroplatinate, and
sodium chloropall'adite, which are used for sensitizing in amounts below that which produces any substantial fog inhibition, as described in Smith and Trivelli U.S. Patent 2,448,060, issued August 31, 1948, and as antifoggants in higher amounts, as described in Trivelli and Smith US. Patents 2,566,245, issued August 28, 1951, and 2,566,263, issued August 28, 1951.
The emulsions can also be chemically sensitized with gold salts as described in Waller et al. US. Patent 2,399,- 083, issued April 23, 1946, and Damschroder et al. US. Patent 2,642,361, issued June 16, 1953. Suitable compounds are potassium chloroaurite, potassium aurithiocyanate, potassium chloroaurate, auric trichloride and 2- aurosulfobenzothiazole methochloride.
The emulsions can also be chemically sensitized with reducing agents such as stannous salts (Carroll U.S. Patent 2,487,850, issued November 15, 1949), polyamines, such as diethylene triamine (Lowe and Jones US. Patent 2,518,698, issued August 15, 1950), polyamines, such as spermine (Lowe and Allen U.S. Patent 2,521,925, issued September 12, 1950), or bis(fl-amiuoethyl) sulfide and its Water-soluble salts (Lowe and Jones US. Patent 2,521,926, issued September 12, 1950).
The emulsions can also be optically sensitized with cyanine and merocyanine dyes, such as those described in Brooker US. Patents 1,846,301, issued February 23, 1932; 1,846,302, issued February 23, 1932; and 1,942,854, issued January 9, 1934; White US. Patent 1,990,507, issued February 12, 1935; Brooker and White US. Patents 2,112,140, issued March 22, 1938; 2,165,338, issued July 11, 1939; 2,493,747 issued January 10, 1950, and 2,739,964, issued March 27, 1956; Brooker and Keyes US. Patent 2,493,748, issued January 10, 1950; Sprague US. Patents 2,503,776, issued April 11, 1950, and 2,519,001, issued August 15, 1950; Heseltine and Brooker U.S. Patent 2,666,761, issued January 19, 1954; Heseltine U.S. Patent 2,734,900, issued February 14, 1956; Van Lare US. Patent 2,739,149, issued March 20, 1956; and Kodak Limited British Patent 450,958, accepted July 15, 1936.
The emulsions can also be stabilized with the mercury compounds of Allen, Byers and Murray U.S. Patent 2,728,663, issued December 27, 1955; Carroll and Murray US. Patent 2,728,664, issued December 27, 1955; and Leubner and Murray US. Patent 2,728,665, issued December 27, 1955; or with gold salts as described in Damschroder US. Patent 2,597,856, issued May 27, 1952,
and Yutzy and Leermakers U.S. Patent 2,597,915, issued 7 May 27, 1952;.the triazoles of Heimbach and Kelly U.S. Patent 2,444,608, issued July 6, 1948; the azaindenes of Heimbach and Kelly U.S. Patents 2,444,605 and 2,444,606, issued July 6', 1948; Heimbach U.S. Patents 2,444,607, issued July 6, 1948, and 2,450,397, issued September 28, 1948; Heimbach and Clark U.S. Patent 2,444,609, issued July 6, 1948; Allen and Reynolds U.S. Patents 2,713,541, issued July 19, 1955, and 2,743,181, issued April 24, 1956; Canroll and Beach U.S. Patent 2,716,062, issued August 23, 1955; Allen and Beilfuss U.S. Patent 2,735,769, issued February 21, 1956; Reynolds and Sagal U.S. Patent 2,756,147, issued July 24, 1956; Allen and Sagura U.S. Patent 2,772,164, issued November 27, 1956, and those disclosed by Birr in Z. Wiss. Phat, vol. 47, 1952, pages 2-28; the disulfides of Kodak Belgian Patent 569,317, issued July 31, 1958; the quaternary benzothiazolium compounds of Brookcr and Stand US. Patent 2,131,038, issued September 27, 1938, or the polymethylene bis-benzothiazolium salts of Allen and Wilson U.S. Patent 2,694,716, issued November 16, 1954; the zinc and cadmium salts of Jones U.S. Patent 2,839,405, issued June 17, 1958; and the carboxymethylmercapto compounds of Murray, Reynolds and Van Allan U.S. Patent 2,819,965, issued January 14, 1958.
The emulsions may also contain speed increasing com- 7 pounds of the quaternary ammonium type of Carroll U.S. Patent 2,271,623, issued February 3, 1942; Carroll and Allen U.S. Patent 2,288,226, issued June 30, 1942; and Carroll and Spence U.S. Patent 2,334,864, issued November 23, 1943; or the polyethylene. glycol type of Carroll and Beach U.S. Patent 2,708,162, issued May 10,195; or the quaternary ammonium salts and polyethylene glycols of Piper U.S. Patent 2,886,437, issued May 12,
1959; as well as the thiopolyrners of Graham and Sagal U.S. application Serial No. 779,839, 'filed December 12, 1958 (now U.S. Patent 3,046,129, issued July 24, 1962), and the Dannv and Chechak U.S. application Serial No. 779,874, filed December 12, 1958 (now U.S. 'Patent 3,046,134, issued July 24, 1962).
T he emulsions may contain .a suitable gelatin plasticizer such as glycerin; a dihydroxy alkane such as 1,5-pentane diol as described in Milton and Murray U.S. application Serial No. 588,951, filed June 4, 1956 (now U.S. Patent 2,960,404, issued November 15, 1960); an ester of an ethylene bis-glycolic acid such as ethylene bis(methyl glycolate) as described in Milton U.S. Patent 2,904,434, issued September 15, 1959; bis-(ethoxy diethylene glycol) succinate as described in Gray U.S. application Serial No. 604,333, filed August 16, 1956 (now U.S. Patent 2,940,854, issued June 14, 1960), or a polymeric hydrosol as results from the emulsion polymerization of a mixture of an amide of an acid of the acrylic acid series, an acrylic acid ester'and a styrene-type compound as described in Tong U.S. Patent 2,852,386, issued September 16, 1958. The plasticizer may be added to the emulsion before or after the addition of a sensitizing dye, if used.
The emulsions may be hardened with any suitable hardener for gelatin such as formaldehyde; a halogen-substituted aliphatic acid such as mucobromic acid as described in White U.S. Patent 2,080,019, issued May 11, 1937; a compound having a plurality of acid anhydride groups such as 7,8-diphenylbicyclo(2,2,2) 7 octene- 2,3,5,6-tetra-carboxylic dianhydride, or a dica'rboxylic or adisulfonic acid chloride such as terephthaloylchloride as described in Allen and Carroll U.S. Patents 2,725,294, and 2,725,295, both issued November 29, 1955; a cyclic 1,2-diketne such as cyclopentane-1,2-dione as described 7 in Allen and Byers U.S. Patent 2,725,305, issued November 29, 1955; (a bisester of methane-sulfonic acid such as 1,2-di-(methanesulfonoxy)-ethane as described in Allen and Laakso U.S. Patent 2,726,162, issued December 6,
1955 1,3 dihydroxymethylbenzimidazol 2 one as described in July, Knott and Pollak U.S. Patent 2,732,316, issued January 24, 1956; a dialdehyde or a sodium bisulfite derivative thereof, such as [i-rnethyl glutaraldehyde 8 V bis-sodium bisulfite as described in Allen and Burness U.S. patent application Serial Nov 556,031, filed December 29, 1955 (now abandoned); a bis-aziridine carboxamide such as trimethylene bis(1-aziridine ca-rboxamide) as described in Allen and Webster U.S. patent application Serial No. 599,891, filed July 25, 1956 (now U.S. Patent 2,950,197, issued August 23, 1960); 2,3-dihydroxy dioxane as described in JelTreys U.S. Patent 2,870,013, issued January 20, 1959; or bisisocyanate as described in Henn et a1. U.S. patent application Serial No. 805,357, filed April 10, 1959. e
The emulsions may contain a coating aid such as saponin; a 'lauryl or oleyl monoether of polyethylene glycol as described in Knox and Davis U.S. Patent 2,831,766, issued April 22, 1958; a salt of a sultated and alkylated polyethylene glycol ether as described in Knox and Davis U.S. Patent 2,719,087, issued September 27, 1955; an acylated alkyl taurine such as the sodium salt of N-oleoyl-N-methyl taurine as described in Knox, Twardokus and Davis U.S. Patent 2,739,891, issued March 27, 1956; the reaction product of a dianhydride of tetracar-- boxybutane with an alcohol or an aliphatic amine containing from 8 to 18 carbon atoms which is treated with a base, for example, the sodium salt of the monoester of tetracarboxybutane as described in Knox, Stenberg and Wilson U.S. Patent 2,843,487, issued July 15, 1958; a water-soluble maleopimarate as described in Knox and Fowler U.S. Patent 2,823,123, issued February 11, 1958; an alkali metal salt of a substituted amino acid such as disodium N-(carbo p tert. octylphenoxypentaethoxy)- glutamate as described in Knox and Wilson U.S. patent application Serial No. 600,679, filed July 30, 1956 (now U.S. Patent 3,038,804, issued June 12, 1962); or a sulfosuccinamate such as tetrasodiurn N-(1,2-dicarboxyethyl)- N-octadecyl sulfosuccinamate as described in Knox and I St-enberg U.S. Patent Application Serial No. 691,125, filed October 21, 1957 (now U.S. Patent 2,992,108, issued July 11, 1961), or a sodium salt of an alkylarylpolyether sulfonate of Baldsiefen U.S. Patent 2,600,831, issued June 17, 1952.
The addenda which we have describedmay be used in various kinds of photographic emulsions. In addition to being useful in X-ray and other nonoptically sensitized emulsions they may also be used in orthochromatic, panchromatic, and infrared sensitive emulsions. They may be added to the emulsion before or after any sensitizing dyes which are used. Various silver salts may be used as the sensitive salt such assilver bromide, silver iodide, silver chloride, or mixed silver halides such as silver chlorobromide or silver bromoiodide. The agents maybe used in emulsions intended for color photography, for example, emulsions containing color-forming couplers or emulsions to be developed by solutions containing couplers or other color-generating materials, emulsions of the mixed-packet type, such as described in Godowsky U.S. Patent 2,698,794, issued January 4, 1955; or emulsions of the mixed-grain type, such as described in Carroll and Hanson U.S. Patent 2,592,243, issued April 8, 1952. These agents can also be used in emulsions which form latent images predominantly on the surface of the silver halide crystal or in emulsions which form latent images predominantly inside the silver halide crystal, such as those described in Davey and Knott U.S. Patent 2,592,250, issued Apr-i1 8; 1952.
These may also be used in emulsions intended for use in diffusion transfer processes which utilize the undeveloped silver halide in the nonirnage areas of the negative to form a positive by dissolving the undeveloped silver halideand precipitating it on a receiving layer in 'close proximity to the original silver halide emulsion layer. Such processes are described in Rott U.S. Patent 2,352,014, issued June 20, 1944, and Land U.S. Patents 2,584,029, issued January 29, 1952; 2,698,236, issuedDecember 28, 1 954, and 2,543,181, issued February 27, 19 51; and Yackel' et al. patent application. Serial No.v
586,705, filed May 23, use (now Us. Patent 3,020,155,
issued February 6, 1962). They may also be used in color transfer processes which utilize the diifusion transfer of an image-wise distribution of developer, coupler or dye, from a lightsensitive layer to a second layer, while the two layers are in close proximity to one another. ;Coior processes of this type are described in Land US. Patents 2,559,643, issued July 10, 1951, and 2,698,798, issued January 4, 1955; Land and Rogers Belgian Patents 554,933 and 554,934, granted August 12, 1957; International Polaroid Belgian Patents 554,212, granted July 16, 1957, and 554,935, granted August 12, 1957; Yutzy US. Patent 2,756,142, granted July 24, 1956 and Whitmore and Mader US. patent application Serial No. 734,141; filed May 9, 1958 (now abandoned). They may also be used in emulsions intended for use in a monobath process such as described in Haist et al. US. Patent 2,875,048, issued February 24, 1959, and in webtype processes, such as the one described in Tregillus et al. US. patent application Serial No. 835,473, filed August 24,1959.
In the preparation of the silver halide dispersions employed for preparing silver halide emulsions, there may be employed as the dispersing agent for the silver halide in its preparation, gelatin or some other colloidal material such as colloidal albumin, a cellulose derivative or a synthetic resin, for instance, a poyvinyl compound. Some colloids which may 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 19-26% as described in US. Patent 2,327,808 of Lowe and Clark, issued August 24, 1943; a Water-soluble ethanolamine cellulose acetate as described in Yutzy US. Patent 2,322,685, issued June 15, 1943; a polyacrylamide or an imidized polyacrylamide as described in Lowe, Minsk and Kenyon US. Patent 2,541,474, issued February 13, 1951; zein as described in Lowe US. Patent 2,563,791, issued August 7, 1951; a vinyl alcohol polymer containing urethane carboxylic acid groups of the type described .in Unruh and Smith US.
Patent 2,768,154, issued October 23, 1956; or containing,
cyano-acetyl groups such as the vinyl alcohol-vinyl cyanoacetate copolymer as described in Unruh, Smith and Priest US. Patent 2,888,331, issued October 1, 1957; or a polymeric material which results from polymerizing a protein or a saturated acylated protein with a monomer having a vinyl group as described in Us. Patent 2,852,382, of Illingsworth, Dann and Gates, issued September 16, 1958.
If desired, compatible mixtures of two or more of these colloids may be employed for dispersing the silver halide in its preparation. Combinations of these antifoggants, sensitizers, hardeners, etc., may be used.
As mentioned above, the advantages of our invention are particularly outstanding in reversal color photographic processes. Couplers or color-forming compounds which are soluble in the strongly alkaline developing solutions are well known to those skilled in the art. Typical couplers include the following:
COUPLERS FOR USE IN COLOR DEVELOPERS Cyan couplers:
( 1) S-benzenesulfonamino-l-naphthol (2) 2,4-dichloro-S-benzenesulfamino-l-naphthol (3) 2,4-dichloro-5- (p-toluenesulfamino) -1-naphthol (4) 5-(1,2,3,4-tetrahydronaphthalene 6 sulfonamin)- 1-naphthol 2,4 dichloro-5-(4'-bromodiphenyl-4-sulfonan1ino)- l-naphthol (6) o- B-Naphthalenesulfonamino phenol (7) 5 -(m-nitrohenzenesulfonamino)-1-naphthol (8) 5-(quinolin-S-sulfonamino)-1-naphthol (9) Z-acetylamino-S-methylphenol (10) 2-benzoylamino-3,S-dimethylphenol (1 l) 2-04-(13-1611. amlphenoxy) -n-butyrylan1ino-5- Inethylphenol (12) Z-a- (p-tert. amylphenoxy) -n-butryrylarnino-4- Chloro-S-methylphenol (13) 2-(p-tert. amylphenoxy-pbenzoyl)amino-4-chloro- 5-methylphenol (l4) 2-(4"-tert. amyl-3-phenoxybenzoylamiuo)-3,5-
dimethyl-l-phenol (15) Z-phenylacetylamino-4chloro-5-methylphenol (l6) Z-b-enzoylamino-4-chloro-S-methylphenol (17) 2-anilinoacetylamino-4-chloro-5-methylphenol l8) 2-{4'- [oc- 4"-tert. amylphenoxy) -n-butyry1amino] benzoylamino}-4-chloro-5-methylphenol (19) 2-{4-[3"-(4'-tert. amylphcnoxy)-benzoylamino]- benzoylamino}-4-chloro-5-methylphenol (20) 2-p-nitrobenzoylamino-4-chloro-S-methylphenol (21) 2-m-aminobenzoyl-4-chloro-5-methylphenol (22) 2-acetamino-4-chloro-S-methylphenol (23) 2- (4'-sec. amylbenzamino)-4-chloro-5-- methylphenol (24) 2-(4'-n-amyloxybenzarnino)-4-chloro5- methylphenol Magenta couplers:
(25) 1-phenyl-3-acetylamino-S-pyrazolone (26) 1-phenylo-3propionylamino-S-pyrazolone (27) 1-pheuyl-3-dichloroacetylarnino-S-pyrazolone (28) 1-phenyl-3-benzoylamino-5-pyrazolone (29) 1-phenyl-3 (m-aminobenzoyl) -amino-5-pyrazolone hydrochloride (30) 1-phenyl-3-(diamylbenzoyl)amino-5-pyrazolone (3 1) 1-pl1enylo-3 -phenylcarbamylamino-S-pyrazolone (32) 1-phenyl-3-phenoxyacetylamino-S-pyrazolone (33) 1-phenyl-3-p-aminohenzoylamino-5-pyrazolone (3 4) 1-phenyl-3 o-carboxybenzoyl) amino-S-pyrazolone (35 1-phenyl-3-palmitylamino-S-pyrazolone (36) 1-phenyl-3-(p-sec. amylbenzenesulfonylamino) -5- pyrazolone (37) 1-phenyl-3-[p-(p-sec. amylbenzoyl) aminobenzoylamino]-5-pyrazolone (3 8) 1-m-tolyl-3-[m-(fi-phenylpropionyl) aminobenzoylamino] -5-pyrazolone (39) 1-m-tolyl-3-(2,4-di-tert.butyl-mtolyloxyacetylamino) -5-pyrazolone (40) 1-[p'-(p-tert. butylphenoxy)phenyl] -3-3 [p- (benzoyl-amino -benz0ylamino] -5-pyrazolone (41 1-( p-tert. butylphenoxyphenyl) -3-(p-mamyloxybenzoyl-amino -5-pyrazolone (42) 1- [p-(p'-tert. butlphenoxy)phenyl]-3-(3,5-
dimethoXy-benzoyl) amino-S-pyrazolone (43) 1- [p-(p'-tert. butylphenoxy) phenyl] -3- [m-(ptoluene-sulfonylamino benzoylamino] -5-pyrazolone (44) 1-[p-(3,5-dimethylphenoxy)phenyl]-3--(4-r1- amyloxy-3-methylbenzoylamino -5-pyrazolone (45) 3-(p-nitrophenoxyacetylamino)-1-(2',4',6,-
trichloro-phenyl -5-pyrazolone Yellow couplers:
(46) pa(w-Benz oylacetamino)bcnzenesulfonamide (47) p-(w-Benzoylacetamino) benzenesulfionmethylamide (48) pw-Benzoylacetamino benzenesulfonanilide (49) 4-benzenesulfonamino-w-benzoylacetanilide 50) 4- (p-toluenesulfonamino) w-benzoylacetanilide (51 4- (p-laurybenzenesultonamino)-wbenzoylacetanilide 52) 1,4-di- [pbenzoylacetamino benzenesulfonamino] benzene (53) N,N-di-(p-benzoylacetaminophenyl)benzene- 1,3-disulfonamide (5 4) N- (p-benzoylacetaminophenyl) -4- [p- (benzoylacetamino)-benzenesulfonamido] benzenesulfonamide (55 N -benzoylacetyl-N- Z-benzoylthiazolyl) sulfanilamide (5 6) p-Acetoacetarninobenzenesulfonfi-naphthalide (57) p-Furoylacetaminobenzenesulfon-N- cyclohexylarnide (58) p-(4-ethoxybenzoylaoetamino)benzenesulfonamide (59) Terephthaloyl-bis(p-N-amylsulfonamido) acetanilide (60) p-(Quinoline-8-sulfonamino)-wbenzoylacetanilide (61 p-Acetoacetarnino-o-methylbenzenesulfon-N- anilide (62) N,N-di- (p-benzoylacetaminophenol) naphthalene-1,5-disulfonamide (63 p-(Benzenesulfonamino)benzoylacetone (6 4) N-benzoylaceto-o-anisidine Typical couplers that are primarily useful in the photographic silver halide emulsion layers of our invention comprise the following:
Coupler:
(65) l-hydroxy-Z [6- 2,4'-di-tert. amylphenoxy) -n- -butyl]-naphthamide (U.S. Patent 2,474,293)
(66) 1-hydroxy-4-phenylazo-4'- (p-tert. butylphenoxy)- Z-naphthanilide (U.S. Patent 2,521,908)
(67) 2- (2,4-di-tert. amylphenoxyacetamino -4,6-
dichloro-S-methylphenol (U.S. Patent 2,725,291)
(68) 2- Ot-di-tel't. amylphenoxy-n-butyrylamino) -4,6-
dichloro-t-methylphenol (69) 6-{64- {4-[06-(2,4-dl-L6Yt. amylphenoxy)butyrarnido]- phenoxy}acetamido}-2,4-dichloro-3-methylphenol (70) 2-[3-(2",4"-diamylphenoxy)-acetamid-o]- benzamido-4-chloro-5-methylphenol (71) 1-(2,4',6'-trichlorophenyl)-3-[3"-(2,4-ditert.-amylphenoxyaoetamido) -benzamido pyrazolone (U.S. Patent 2,600,788)
(72) 1-(2,4,6'-tricholrophenyl)-3-[3"-(2",4"-ditert.-amylphenoxyacetamido -benzarnido -4- (pmethoxyphenylazo) -5-pyrazolone (73 N-(4-benzoylacetaminobenzenesulfonyl)-N- (vphenylpropyl) -ptoluidine (U.S. Patent 2,298,443)
(74) wo-Methoxybenzoyl-ot-chloro-4- oc- (2,4-di-tert.-
amy-l-phenoxy)-n-butyrarnido]-acetanilide (McCrossen US. Patent 2,728,658)
(75) oc-{Z- [or-(2,4-di-tert. amylphenoxy) acetamido]- benzoyl}-2-methoxyacetanilide (76) 3-benzoylacetamido-4-methoxy-2,4'-di-tert.-
amylphenoxyacetanilide (77) benzoylacetamido-3-methoxy-2,4'-di-tert.-
amylphenoxyacetanilide Other couplers suitable for use in the emulsions of our invention comprise those disclosed in Spence and Carroll US. Patent 2,640,776, issued June 2, 1953, Weissberger et al. US. Patent 2,407,210, issued September 3, 1946, and Weissberger et al. US. Patent 2,474,293,
issued June 28, 1949.
The color-forming developers useful in our invention have been previously described in the prior art, and our invention is not to be restricted to the use of any particular color-forming developer. The color-forming developers previously mentioned which we have found to be especially useful in our invention. comprise aromatic primary amines containing an amino (substituted or not) or hydroxyl substituent. Phenylenediamines and substituted derivatives thereof containing a primary amino group have been found to provide excellent results when employed in combination with the formamidinothiomethyl compounds of our invention. Typical of such color-forming developers are the sulfonamido substituted p-phenylenediamines disclosed in Weissberger US. Patent 2,548,574, issued April 10,
1951, the substituted p-phenylenediamines disclosed in,
Weissberger et al. US. Patent 2,566,271, issued August 28, 1951. Other phenylenediamine color-forming developers can be employed to like advantage in the process of our invention.
The first developer employed in the process of our invention is generally a rapid developer of the MO type,
i2. i.e., a combination of hydroquinone and Elon (p-N-methylaminophenyl) developer.
The following examples will serve to illustrate the manner of obtaining improved images in multi-layer photographic elements according to our invention.
An ordinary photographic multi-layer color film of the type described in Mannes et al. US. Patent 2,252,718
and containing no color-formers or couplers in the selec i tively sensitized photographic silver halide emulsion layers (i.e., blue, green and red) was cut into a number of strips. Each of the strips was then exposed for A second on an Eastman Type Ib Sensitometer to a 500- watt light source equipped with a 0.6 neutral density filter in combination with a Wratten No. 29 filter (i.e., a filter transmitting only visible light beyond about 600 m with maximum transmitttance at about 700 m so that the illuminant had a color temperature of about 3000 K. Each of the strips was then developed to a black-andwhite negative image by development for 10 minutes at 80 F. in an ordinary hydroquinone-Elon developer, such as one having the following formula:
Kodak developer D-19 Grams N-methyl-p-aminophenol sulfate 2.0 Sodium sulfite, desiccated 90.0 Hydroquinone 8.0 Sodium carbonate, monohydrated 52.5 Potassium bromide 5.0
Cold water to make 1.0 liter.
The strips were then washed for 2 minutes at 80 F., followed by an additional two minutes treatment at 80 F. in a fog-reducing bath having the following composition:
3- (2-benzothiazolylmethyl benzothioazolin p-toluenesulfonate "grams" 0.5 Methanol cc Water cc 900 Each of the strips was then again washed for two minutes with water heated to 80 F. and given reversal reexposure for 15 seconds to a RFL No. 2 Lamp placed at a distance of one meter through a Wratten No. 92
filter (i.e., a filter transmitting only visible radiation beyond about 620 III/.1. with maximum transmittance of about 88 percent at 700 mu.
Each of the strips was developed for ten minutes at 80 F. in a cyan developer having the composition given below. One of the film strips served as a control and contained no thioether compound, while the other strips were developed in cyan developers containing thioether compounds in amounts identified in the following table. The compound numbers in the table correspond to the compound numbers given above for the thioether compounds. The cyan developer which served as a control and to which the thioether compounds were added had the following formula:
Sulfuric acid (concentrated) ce 1.5 Calgon (sodium hexametaphosphate) grams 0.5 Sodium sulfite do 5.0 2-amino-5-diethylamino toluene.HCl do 0.6 Sodium carbonate monohydrate do 15.0 Sodium bromide do 0.25 Potassium iodide "do-.." .002 Color coupler 1 -do 1.2 H acid do 0.5
Water to 1 liter. (Sufficient sodium hydroxide added to give a pH of 10.5.)
1 5-pt0lueue sulfonamido-Z,4-dichloro-a-naphthol.
Each of the strips was then washed for 10 minutes in l3 water heated to 80 F. and bleached for two minutes at 80 F. in a bath having the following composition:
Grams Calgon 1.0 Potassium ferricyanide 80.0 Sodium bromide 34.4
Water to 1 liter.
The strips were then fixed for two minutes at 80 F. in a bath having the following composition:
Grams Calgon 10.0 Soduim sulfite 10.0 Sodium thiosulfate pentahydrate 320 Water to make 1 liter.
The strips were then washed for five minutes in 80 F. water and dried. The following results were obtained.
+ exceeds scale of densitometer.
During the development of a color film such as described above in a black-and-white developer, fog centers are introduced in the unexposed regions which then develop in the coupler containing developers. For example, after negative development and red re-exposure, development in a color developer containing a cyan coupler results not only in development of the red sensitive layer, but also in development of cyan fog in the blueand green-sensitive layers. Such cyan fog is tabulated in the table above.
The following example will serve to illustrate the useful effect of our thioether compound in a magenta reversal developer.
A multi-layer color film of the type used in Example 1 was cut into several strips and each of these exposed for second to a SOD-watt 3000 K. light source on an Eastman Type Ib Sensitometer. Each of the strips was then developed for nine minutes at 80 F. to a black-andwhite negative developer of the type described in the above example and washed for five minutes in 80 F. water. Strips were then treated in an antifoggant bath of the type described in the above example for two minutes at 80 F. and washed for two minutes in 80 F.
water. The strips were then given a reversal re-exposure to red illumination as described in Example 1 and developed for minutes at 80 F. in the above cyan developer containing no thioether compound. The strips were then washed for five minutes at 80 F. in water and exposed to blue illumination through the emulsion side of the support and developed for minutes at 80 F. in a yellow-forming developer having the following composition:
Water to make 1 liter. (Suliicient sodium hydroxide to give a pH of 11.5.)
14 The strips were again Washed for 5 minutes at F. in Water and given a flash exposure to white light and developed in a magenta developer for the times indicated in the following table, the developing composition being as follows:
Grams Sulfuric acid (concentrated) 1.5 Calgou 0.5 Sodium sulfite 5.0 Z-aminO-Sdiethylamino toluene HCI 1.6 Sodium carbonate monohydrate 15.0 Sodium bromide 0.25 Potassium iodide 0.002 Coupler 4.0 H acid 0.2
Water to make 1 liter. (Suflicient sodium hydroxide to give a pH of 11.0.)
1 1-(2,4,6-trichloropheny1) 3[a nitrophenoxy)-acetamide 5-py1'azolone. The strips were then washed for 5 minutes in 80 F. Water, bleached for 2 minutesat 80 F. in the bleach bath of the above example, fixed for two minutes at 80 F. in a fixing bath or" the type used in the above example, washed for five minutes at 80 F. and dried. The following data were obtained:
0 TABLE 11 Gone. in Magenta Magenta Compound Number Magenta Dev. max
Dev., g./l. Time,
Minutes Control- 20 2. 26 2. 0 l5 3. 30
wherein R represents a member selected from the class consisting of a hydroxyl group, an alkoxyl group, and a carbamyl group, R represents an ethylene radical, X represents a divalent radical selected from the class consisting of an oxygen atom, a sulfur atom and the group X CH CH X X and X each represents a divalent radical selected from, the class consisting of an oxygen atom and a sulfur atom, provided at least one of the radicals selected from the class consisting of X, X and X represents a sulfur atom, X represents the divalent radical d represents a positive whole number of from 1 to 2 and n represents a positive whole number of from 1 to 3.
2. A photographic color developer comprising an aquous alkaline solution of a p-phenylenediamine color developing agent, a color-forming compound capable of coupling with the oxidation products of said color developing agent to provide a colored image, and a non-pol l V ymeric compound selected from those represented by the following general formula:
wherein R represents a member selected from the class consisting of a hydroxyl group, an alkoxyl group, and a carbamyl group, R represents an ethylene radical, X represents a divalent radical selected from the class consisting of an oxygen atom, a sulfur atom,
and the group X CH CH X1, X and X each represents a divalent radical selected from the class consisting of an oxygen atom and a sulfur atom, provided at least one of the radicals selected from the class consistmg of X, X and X represents a sulfur atom, X represents the divalent radical wherein R represents a member selected from the class consisting of a hydroxyl group, an alkoxyl group and a carbamyl group, X represents a divalent radical selected from the class consisting of an oxygen atom, a sulfur atom,
lNHCH NH( iand the radical -X CH CH X X and X each represents a divalent radical selected from the class consisting of an oxygen atom and a sulfur atom, provided at least one of the radicals selected from the class consisting of X, X and X represents a sulfur atom, and n represents a positive Wholenumber of from 1 to 3.
4. A photographic color developer comprising an aqueous alkaline solution, of a p-phenylenediamine color developing agent, a phenolic compound capable of coupling with the oxidation products of said color developing agent to provide a cyan photographic image, and a nonpolymeric compound selected from those represented by the following general formula:
X[-oH C1-I2X2ort ii 0 (CH2CH2 )nl l ]2 wherein R represents a member selected from the class consisting of a hydroxyl group, an :alkoxyl group, and a caroamyl group, R represents an ethylene radical, X represents a divalent radical selected from the class con- 'sisting of an oxygen atom, a sulfur atom,
I ll 7 -C|NHCI-I2NHC- and the radical X CH CH X X and X each represents a divalent radical selected from the class consisting of an oxygen atom and a sulfur atom, provided at least one of the radicals selected from the class consisting of X, X and X represents a sulfur atom, and n represents a positive whole number of from 1 to 3.
' 5. A photographic color developer comprising an aqueous alkalinesolution of a p-phenylenediamine color developing agent, a compound capable of coupling with the oxidation products of said color developing agent to produce a colored photographic image, and a non-polymeric compound selected from those represented by the following general formula:
wherein R and R each represents a hydrocarbon alkylene group containing from about 2 to 10 carbon atoms and d represents a positive integer of from 1 to 3.
6. A photographic color developer comprising an aqueous alkaline solution of a p-phenylenediamine color de veloping agent, a compound capable of coupling with'the oxidation products of said color developing agent to produce a colored photographic image, and a non-polymeric compound selected from those represented by the following general formulai wherein m and it each represents a positive integer of from about 2 to 10.
7. A photographic color developer comprising an aqueous alkaline solution of a p-phenylenediamine color developing agent, a pyrazolone compound capable of coupling with the oxidation products of said color developing agent to produce a magenta photographic image and a non-polymeric sompound selected from those represented by the following general formula:
v I-lO-R(-'SR S'-ROH wherein R and R each represents a hydrocarbon alkylene group containing from about 2 to 10 carbon atoms and d represents a positive integer of from 1 to 3.
8. A photographic color developer comprising an aqueous alkaline solution of an arylenediamine color developer and the compound having the formula:
HOCH CH SCH CI-l OCH CH 0CH CH SCH CH OH 9. A photographic color developer comprising an aqueous alkaline solution of an arylenediamine color developer and the compound having the formula:
V cn crr oon,cn ocn cn scn cn OQH CH SCH CH OCH CH OCH CH ltl. A photographic color developer comprising an aqueous alkaline solution of an arylenediamine color developer and'the compound having'the formula:
CH OCH CH SCH CH OCH 11. A photographic color developer comprising an aqueous alkaline solution of an arylenediamine color deveioper and the compound having the formula:
CH CH OCH CH SCH CH OCH CH GCH CH SCH CH OCPL,
12. A photographic color developer comprising an aqueous alkaline solution of an arylenediamine color de veloper and the compound having the formula:
ll ((3 5 0 OH CH SCH CH CNI-I) OH;
References Cited by the Examiner UNITED STATES PATENTS NORMAN o. roacnns, Primary Eramiizer HAROLD N. BURSTEIN, Examiner.
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,201,242 August 17, 196
Judith A. Schwan et a1.
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 16, lines 53 and 54, the right-hand portion of th formula reading CH OCH CH SCH CH OCH read CH OCH CH SCH CH OCH CH Signed and sealed this 8th day of March 1966.
(SEAL) Attcst:
ERNEST W. SWIDER EDWARD J. BRENNER Attesting Officer Commissioner of Patents

Claims (1)

1. A PHOTOGRAPHIC COLOR DEVELOPER COMPRISING AN AQUEOUS ALKALINE SOLUTION OF AN ARYLENEDIAMINE COLOR DEVELOPER AND A NON-POLYMERIC COMPOUND SELECTED FROM THOSE REPRESENTED BY THE FOLLOWING GENERAL FORMULA:
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DEE23468A DE1147845B (en) 1961-09-11 1962-09-01 Color developer for reverse color development of photographic material
FR908771A FR1351410A (en) 1961-09-11 1962-09-06 New developer for color photography
GB22017/65A GB1020033A (en) 1961-09-11 1962-09-07 Photographic silver halide colour developers and processes of producing reversed colour developed photographic images
GB34357/62A GB1020032A (en) 1961-09-11 1962-09-07 Photographic colour developers and processes of producing reversed colour developed photographic images

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US3419392A (en) * 1965-02-24 1968-12-31 Ilford Ltd Thioether silver halide development accelerators
JPS5763530A (en) * 1980-10-03 1982-04-17 Fuji Photo Film Co Ltd Method of development processing of color photographic material
US4525449A (en) * 1982-11-01 1985-06-25 Fuji Photo Film Company, Limited Method of treatment of color photographic materials
WO1987004533A1 (en) 1986-01-23 1987-07-30 Fuji Photo Film Company Limited Process for forming colored image
WO1988000724A1 (en) * 1986-07-10 1988-01-28 Konica Corporation Process for processing silver halide color photographic materials and color developer for use in said process
US4752560A (en) * 1985-09-24 1988-06-21 Eastman Kodak Company Photographic element containing a cyclic thioether compound
US5079133A (en) * 1986-04-11 1992-01-07 Fuji Photo Film Co., Ltd. Silver halide color photographic material
USH1020H (en) 1989-09-25 1992-02-04 Konica Corporation Developing solution for light-sensitive silver halide photographic material and method of forming photographic image making use of it
US5344750A (en) * 1992-05-12 1994-09-06 Fuji Photo Film Co., Ltd. Color development processing method of silver halide color photographic material using a color developer where the color developing agent concentration and processing temperature are a function of bromide ion concentration
US5633124A (en) * 1992-05-08 1997-05-27 Eastman Kodak Company Acceleration of silver removal by thioether compounds
US5789143A (en) * 1997-04-30 1998-08-04 Eastman Kodak Company Thioethers in photographic elements

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US3581146A (en) * 1969-07-29 1971-05-25 Alan E Hill Ballast for a plurality of parallel gaseous discharges
US4254919A (en) * 1980-05-12 1981-03-10 Polaroid Corporation Method of loading film cassette
JPS59188641A (en) 1983-04-11 1984-10-26 Fuji Photo Film Co Ltd Silver halide photographic emulsion
US4960683A (en) * 1987-06-29 1990-10-02 Fuji Photo Film Co., Ltd. Method for processing a black-and-white photosensitive material
US5616446A (en) 1994-09-29 1997-04-01 Konica Corporation Silver halide photographic light-sensitive material
JP3448724B2 (en) 1995-11-29 2003-09-22 コニカ株式会社 Developer for silver halide photographic material and processing method thereof
WO2012035314A1 (en) 2010-09-17 2012-03-22 Fujifilm Manufacturing Europe Bv Photographic paper
GB202006061D0 (en) 2020-04-24 2020-06-10 Fujifilm Mfg Europe Bv Photographic paper

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US3021215A (en) * 1959-10-01 1962-02-13 Eastman Kodak Co Polythialkylenediols as sensitizers for photographic silver halide emulsions
US3038805A (en) * 1959-10-14 1962-06-12 Eastman Kodak Co Non-polymeric open-chain sensitizers
US3046129A (en) * 1958-12-12 1962-07-24 Eastman Kodak Co Sensitization of photographic silver halide emulsions containing colorforming compounds with polymeric thioethers

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US3046129A (en) * 1958-12-12 1962-07-24 Eastman Kodak Co Sensitization of photographic silver halide emulsions containing colorforming compounds with polymeric thioethers
US3021215A (en) * 1959-10-01 1962-02-13 Eastman Kodak Co Polythialkylenediols as sensitizers for photographic silver halide emulsions
US3038805A (en) * 1959-10-14 1962-06-12 Eastman Kodak Co Non-polymeric open-chain sensitizers

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3419392A (en) * 1965-02-24 1968-12-31 Ilford Ltd Thioether silver halide development accelerators
JPS5763530A (en) * 1980-10-03 1982-04-17 Fuji Photo Film Co Ltd Method of development processing of color photographic material
JPS6232463B2 (en) * 1980-10-03 1987-07-15 Fuji Photo Film Co Ltd
US4525449A (en) * 1982-11-01 1985-06-25 Fuji Photo Film Company, Limited Method of treatment of color photographic materials
US4752560A (en) * 1985-09-24 1988-06-21 Eastman Kodak Company Photographic element containing a cyclic thioether compound
WO1987004533A1 (en) 1986-01-23 1987-07-30 Fuji Photo Film Company Limited Process for forming colored image
US5079133A (en) * 1986-04-11 1992-01-07 Fuji Photo Film Co., Ltd. Silver halide color photographic material
WO1988000724A1 (en) * 1986-07-10 1988-01-28 Konica Corporation Process for processing silver halide color photographic materials and color developer for use in said process
AU597408B2 (en) * 1986-07-10 1990-05-31 Konishiroku Photo Industry Co., Ltd. Processing silver halide colour photographic materials
US4937178A (en) * 1986-07-10 1990-06-26 Konica Corporation Processing method for silver halide color photographic light-sensitive material and color developer used therein
USH1020H (en) 1989-09-25 1992-02-04 Konica Corporation Developing solution for light-sensitive silver halide photographic material and method of forming photographic image making use of it
US5633124A (en) * 1992-05-08 1997-05-27 Eastman Kodak Company Acceleration of silver removal by thioether compounds
US5344750A (en) * 1992-05-12 1994-09-06 Fuji Photo Film Co., Ltd. Color development processing method of silver halide color photographic material using a color developer where the color developing agent concentration and processing temperature are a function of bromide ion concentration
US5789143A (en) * 1997-04-30 1998-08-04 Eastman Kodak Company Thioethers in photographic elements

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