US2828203A - Method of increasing clayden desensitization of photographic emulsions - Google Patents

Method of increasing clayden desensitization of photographic emulsions Download PDF

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US2828203A
US2828203A US440283A US44028354A US2828203A US 2828203 A US2828203 A US 2828203A US 440283 A US440283 A US 440283A US 44028354 A US44028354 A US 44028354A US 2828203 A US2828203 A US 2828203A
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clayden
exposure
emulsion
intensity
density
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US440283A
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Edgar A Macwilliam
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Eastman Kodak Co
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Eastman Kodak Co
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Priority to US440283A priority patent/US2828203A/en
Priority to GB17105/55A priority patent/GB773388A/en
Priority to DEE10923A priority patent/DE1022090B/en
Priority to FR1126802D priority patent/FR1126802A/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
    • G03C1/00—Photosensitive materials
    • G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/36—Desensitisers
    • 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
    • G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/08—Sensitivity-increasing substances
    • G03C1/10—Organic substances
    • G03C1/12—Methine and polymethine dyes
    • G03C1/22—Methine and polymethine dyes with an even number of CH groups
    • 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
    • G03C1/485—Direct positive emulsions
    • G03C1/48592—Positive image obtained by various effects other than photohole bleaching or internal image desensitisation, e.g. Sabatier, Clayden effect
    • 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
    • Y10S430/141—Direct positive material

Definitions

  • This invention relates. to. photography and particularly to a method of increasing the susceptibility of silver halide emulsions to Clayden desensitization.
  • Clayden effect The feature which characterizes the Clayden effect is that the initial exposure of short duration to relatively high intensity light densensitizes the emulsion so that subsequent exposure to weak intensity light produces less effect than if the pre-exposure had not been given. As usually observed, .the density resulting from the two superposed exposures is less than that of the single exposure to the low intensity light.
  • the elfect known as the Clayden effect has a number of practical applications. Yule and Maurer have described in'their U. S. Patent 2,691,5 86 use of the Clayden effect in preparing a pre-screened photographic material With which halftone negatives may be prepared from a continuous tone original without the use of the conventional halftone screen.
  • the usefulness of such prescreened materials in the graphic arts for letterpress, lithographic and intaglio printing depends on the degree of desensitization obtainable and hence, on the degree of sensitivity of the material to the Clayden elfect.
  • the emulsions which I use are those which initially, that is, without merocyanine or hemioxonol dye, are Clayden desensitizable to some degree and by the addition of these dyes become Clayden desentitizable to a useful degree.
  • a silver halide emulsion which when exposed under a step tablet having 28 steps starting with approximately zero density and increasing in intervals of 0.3 density, to light from a high intensity flash lamp having 18,000 lumen seconds output in .0005 sec- 0nd, two feet from the emulsion, and without intermediate treatment is again exposed with the step tablet rotated 90,'to light from a 1000 watt tungsten lamp two feet from the emulsion, for two minutes, shows at least 0.10 log E or /3 step decrease in density between an area receiving only low intensity exposure and an area receiving the same level of low intensity exposure plus some level of high intensity exposure, when developed 1 rent 0 "ice for 2% minutes at 68 F. in a developer of the following composition:
  • a suitable emulsion at any stage before coating a merocyanine or hemioxonol dye having one of the following formulas where X represents the atoms necessary to complete one of the following nuclei:
  • R represents an alkyl radical, e. g., methyl or ethyl.
  • Compound 1 is Example a
  • compound 2 is Example 11
  • compound 4 is Example 9
  • compound 6 is Example 10 2,828,203 7 V c V"
  • compound 9 is Example 15b of that patent.
  • Compound 5 is prepared as described in Brooker and White U. S. Patent 2,165,338, being Example 7 of that patent.
  • Compounds 11 and 12 are prepared as described in Keyes U. S. Patent 2,186,608.
  • Example 1 To portions of a gelatino-silver halide emulsion which showed minimum Clayden effect when coated without sensitizing dye, there was added increasing amounts of l carboxymethyl 5 [(3 ethyl 2(3H) benzoxazolylidene) ethylidene] 3 phenyl 2 thiohydantoin. The separate emulsions were coated on film support, dried and prefiashed to a short duration (.0001 second) exposure to a high intensity flash lamp of approximately 18,000 lumen seconds'output, followed by an intensity scale exposure of 30 seconds duration to light from a 1000 watt tungsten lamp two feet from the emulsion. The test strips were developed 2 /2 minutes at 68 F. in the developer listed above, and the sensitivity decreasewas determined in each of the samples with the following result:
  • sion according to my invention provides a useful increase in the degree of desensitization which can be obtained.
  • Example 2 A coating was made and treated as in Example 1, but using as the sensitizing dye 1-carboxymethyl-5-[(3- methyl 2(3H) thiazolinylidene)isopropylidene] 3- phenyl-Z-thiohydantoin. The following results were obtained:
  • Example 3 Desensitization Amount of dye, mgJmole Ag halide
  • Example 3 A coating was made as in Example 1 containing 0.2 g. of the sensitizing dye per mole of silver, dissolved in methyl amine and alcohol. This coating was exposed by contact through a positive transparency to light from a Kodatron flash lamp (high intensity electronic flash of duration about 0.0001 second) at 2 feet. It was then given a general exposure to a 40 watt incandescent .bulb at 5 feet for 20 seconds. 20 seconds in a developer of the following compositio and a positive copy resulted. l
  • Example 4 A series of coatings was made as in Example 1, containing the indicated amounts of the following sensitizing dyes per mole of silver halide. When exposed and processed as in Example 1, the following results were obtained:
  • the emulsions which I have prepared, while intended to produce a positive reproduction of the subject by means of the Clayden effect as des-cibed in the above examples, may also be used to produce a negative image by exposure either to the high intensity light source or to a low intensity light source but not both, and development in the customary manner.
  • the composition of the developing solution is not critical (as long as the emulsion has the required properties, that is, is Clayden desensitizable) and my results may even be obtained with color developers containing the customary coupling or color-forming components.
  • the method of obtaining a direct-positive image in a silver halide emulsion layer which comprises imagewise exposing to a high intensity short duration flash of suflicient intensity and sufficiently short duration to produce a Clayden desensitization a silver halide emulsion which when exposed under a step tablet having 28 steps starting with approximately zero density and increasing in intervals of 0.3 density, to a light from a high intensity flash lamp having 18,000 lumen seconds output in .0005 second, two feet from the emulsion, and again exposed with the step tablet rotated 90, to low intensity light from a 1000 watt tungsten lamp 2 feet from the emulsion for 2 minutes, shows at least 0.10 log E decrease in density between an area receiving only low intensity exposure and an area receiving the same level of low intensity exposure plus some level of high intensity exposure, when developed for 2% minutes at.68 F. in a developer of the following composition:
  • X representsthe atoms necessary to complete a nucleus selected from the class consisting of thiazole, thiazoline, benzothiazole, naphthothiazole, benzoxazole, naphthoxazole and quinoline
  • R is selected from the class consisting of hydrogen and'alkyl radicals
  • R is an alkyl radical
  • Y represents the atoms necessary to complete a nucleus selected from the class consisting of rhodanine, thiohydantoin and 2-thio-oxaz0lidinedione nuclei, then uniformly exposing said emulsion layer to a light source of sufiiciently low intensity and for a sufiiciently long time to produce a developable density in regions of said emulsion that received no high intensity exposure, and developing a positive image in said emulsion layer with a silver halide developing agent.

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  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
  • Plural Heterocyclic Compounds (AREA)

Description

States NIETHOD OF INCREASING CLAYDEN DES ENSI- TIZATION OF PHOTOGRAPHIC EMULSIONS No Drawing. Application June 29, 1954 Serial No..440,283
Claims. (Cl. 96-27) This invention relates. to. photography and particularly to a method of increasing the susceptibility of silver halide emulsions to Clayden desensitization.
It has been shown that the sensitivity of some photographic materials when exposed by a relatively long duration exposure may be reduced if the materials have first been exposed to illumination of short duration, i. e. 0.001 second or less. This effect has been called the Clayden effect. The feature which characterizes the Clayden effect is that the initial exposure of short duration to relatively high intensity light densensitizes the emulsion so that subsequent exposure to weak intensity light produces less effect than if the pre-exposure had not been given. As usually observed, .the density resulting from the two superposed exposures is less than that of the single exposure to the low intensity light.
The elfect known as the Clayden effect has a number of practical applications. Yule and Maurer have described in'their U. S. Patent 2,691,5 86 use of the Clayden effect in preparing a pre-screened photographic material With which halftone negatives may be prepared from a continuous tone original without the use of the conventional halftone screen. The usefulness of such prescreened materials in the graphic arts for letterpress, lithographic and intaglio printing depends on the degree of desensitization obtainable and hence, on the degree of sensitivity of the material to the Clayden elfect.
Frequently the Clayden effect desensitization produced in an emulsion is not sufiiciently great to give a commercially useful result. It is therefore the principal object of my invention to provide a novel method of increasing thesusceptibility of the emulsion to Clayden desen sitization. Other objects will appear from the following description of my invention. 7 r
' These objects are accomplished, by incorporating in a silver halide emulsion which shows at least some susceptibility to Clayden desensitization, a merocyanine or hemioxonol dye of the class hereinafter defined.
The emulsions which I use are those which initially, that is, without merocyanine or hemioxonol dye, are Clayden desensitizable to some degree and by the addition of these dyes become Clayden desentitizable to a useful degree. By Clayden desensitizable to some degree, I mean that a silver halide emulsion is used which when exposed under a step tablet having 28 steps starting with approximately zero density and increasing in intervals of 0.3 density, to light from a high intensity flash lamp having 18,000 lumen seconds output in .0005 sec- 0nd, two feet from the emulsion, and without intermediate treatment is again exposed with the step tablet rotated 90,'to light from a 1000 watt tungsten lamp two feet from the emulsion, for two minutes, shows at least 0.10 log E or /3 step decrease in density between an area receiving only low intensity exposure and an area receiving the same level of low intensity exposure plus some level of high intensity exposure, when developed 1 rent 0 "ice for 2% minutes at 68 F. in a developer of the following composition:
Grams Hydroquinone 22.2 Sodium sulfite, desiccated 30 Paraformaldehyde 7.5 Potassium metabisulfite 2.6 Boric acid, crystals 7.5 Potassium bromide 1.6
Water to 1 liter.
According to my inventionl add to a suitable emulsion at any stage before coating a merocyanine or hemioxonol dye having one of the following formulas where X represents the atoms necessary to complete one of the following nuclei:
and R represents an alkyl radical, e. g., methyl or ethyl.
The following dyes may be used according to my invention: V r
1-carhoxymethyl-5-[ (3-ethy1-2 3H )'-benzoxazolylidene) ethylidene1-3-phenyl- -thiohydantoin 1-carboxymethy1-5-[ fi3-ethyl-2 (3H) -benzothiazo1y11dene )1 ethylidene -3-pheny1-2-thiohydantolu 3-carboxymethy1-5-[B- 3-ethyl-2 (3H) -benzothiazo1y11dene) ethylidene] -rhodanine 3-ethyl-5-(3-ethyl-2 (3H -benzothiazolylidene-isopropylidene) 2-thio-.-,4 (3,5 -oxazoledione C=CHCH=C N-CHzCO OH =s C2115 3ca.rboxymethyl-5-[B- (8-ethyl-2(3H)-benzoxazo1y1idene)- ethylidene] -rhodanine 1-carb0xymethy1-5-[ (3-methyl-2 3H -thiazolinylidene) isopropylidenej-3-phenyl-2-thiohydantoin 3-carboxymethyl-5J 3-methyl-2 (3H -thiazoly1idene) isopropylidene] -rl1odamne 3-ethyl-1-phenyl-5- ['y- (l-plperldyl) allylidene] -2-thiohydantoin Compounds 1 to 4 and 6 to are prepared as described in Brooker and Keyes U. S. Patent 2,493,748. Compound 1 is Example a, compound 2 is Example 11, compound 4 is Example 9, compound 6 is Example 10 2,828,203 7 V c V" and compound 9 is Example 15b of that patent. Compound 5 is prepared as described in Brooker and White U. S. Patent 2,165,338, being Example 7 of that patent. Compounds 11 and 12 are prepared as described in Keyes U. S. Patent 2,186,608.
My invention will be further illustrated by reference to the following examples:
Example 1 To portions of a gelatino-silver halide emulsion which showed minimum Clayden effect when coated without sensitizing dye, there was added increasing amounts of l carboxymethyl 5 [(3 ethyl 2(3H) benzoxazolylidene) ethylidene] 3 phenyl 2 thiohydantoin. The separate emulsions were coated on film support, dried and prefiashed to a short duration (.0001 second) exposure to a high intensity flash lamp of approximately 18,000 lumen seconds'output, followed by an intensity scale exposure of 30 seconds duration to light from a 1000 watt tungsten lamp two feet from the emulsion. The test strips were developed 2 /2 minutes at 68 F. in the developer listed above, and the sensitivity decreasewas determined in each of the samples with the following result:
sion according to my invention provides a useful increase in the degree of desensitization which can be obtained.
Example 2 A coating was made and treated as in Example 1, but using as the sensitizing dye 1-carboxymethyl-5-[(3- methyl 2(3H) thiazolinylidene)isopropylidene] 3- phenyl-Z-thiohydantoin. The following results were obtained:
Desensitization Amount of dye, mgJmole Ag halide Example 3 A coating was made as in Example 1 containing 0.2 g. of the sensitizing dye per mole of silver, dissolved in methyl amine and alcohol. This coating was exposed by contact through a positive transparency to light from a Kodatron flash lamp (high intensity electronic flash of duration about 0.0001 second) at 2 feet. It was then given a general exposure to a 40 watt incandescent .bulb at 5 feet for 20 seconds. 20 seconds in a developer of the following compositio and a positive copy resulted. l
Grams- N-rnethyl-p-aminophenol sulfate 2.2- Hydroquinone 9 Sodium sulfite (desiccated) 96 Sodium carbonate (desiccated) 48 Potassium bromide 5 Water to 1 liter.
The film was developed for Example 4 A series of coatings was made as in Example 1, containing the indicated amounts of the following sensitizing dyes per mole of silver halide. When exposed and processed as in Example 1, the following results were obtained:
Desens. mg. Log E Dye Dye/mole Measured Ag Halide at a Density of 1.0
No dye 0. 05 1 Oarboxymethyl -5- [(3 ethyl 2(3H) benzoxazolylidene) ethylidene} 3 -phenyl 2 thiohydantoin 75 0. 75 Do 150 1. 3-Carboxymethyl 5 [B (3 ethyl 2(3H) benzoxazolylidene) -ethylidene]rhodanine 75 0. 55 Do 150 2. 30 3 Garboxymethyl 5 [(3 methyl 2(3H)- thiazolylidene)iso-propylidene1rhodanine. 75 0. 32 Do 150 2. 50
The emulsions which I have prepared, while intended to produce a positive reproduction of the subject by means of the Clayden effect as des-cibed in the above examples, may also be used to produce a negative image by exposure either to the high intensity light source or to a low intensity light source but not both, and development in the customary manner. The composition of the developing solution is not critical (as long as the emulsion has the required properties, that is, is Clayden desensitizable) and my results may even be obtained with color developers containing the customary coupling or color-forming components.
It will be understood that the examples included herein are illustrative only and that my invention is to be taken as limited only by the scope of the appended claims.
I. claim:
1. The method of obtaining a direct-positive image in a silver halide emulsion layer, which comprises imagewise exposing to a high intensity short duration flash of suflicient intensity and sufficiently short duration to produce a Clayden desensitization a silver halide emulsion which when exposed under a step tablet having 28 steps starting with approximately zero density and increasing in intervals of 0.3 density, to a light from a high intensity flash lamp having 18,000 lumen seconds output in .0005 second, two feet from the emulsion, and again exposed with the step tablet rotated 90, to low intensity light from a 1000 watt tungsten lamp 2 feet from the emulsion for 2 minutes, shows at least 0.10 log E decrease in density between an area receiving only low intensity exposure and an area receiving the same level of low intensity exposure plus some level of high intensity exposure, when developed for 2% minutes at.68 F. in a developer of the following composition:
. Grams Hydroquinone 22.2 Sodium sulfite, desi d 30 Paraformaldehyde 7.5 Potassium metahisnlfite 2 Boric acid, crystals 7.5 1.6
Potassium bromide Water to 1 liter.
6 said emulsion containing an appreciable amount of a dye selected from dyes having the general formulas:
where X representsthe atoms necessary to complete a nucleus selected from the class consisting of thiazole, thiazoline, benzothiazole, naphthothiazole, benzoxazole, naphthoxazole and quinoline, R is selected from the class consisting of hydrogen and'alkyl radicals, R is an alkyl radical, and Yrepresents the atoms necessary to complete a nucleus selected from the class consisting of rhodanine, thiohydantoin and 2-thio-oxaz0lidinedione nuclei, then uniformly exposing said emulsion layer to a light source of sufiiciently low intensity and for a sufiiciently long time to produce a developable density in regions of said emulsion that received no high intensity exposure, and developing a positive image in said emulsion layer with a silver halide developing agent.
2. The method of claim 1, in which the dye is l-carboxymethyl 5 [(3 ethyl 2(3H) benzoxazolylidene)ethylidene]-3-phenyl-2-thiohydantoin.
3. The method of claim 1, in which the dye is 3-carboxymethyl 5 [B (3 ethyl 2(3H) benzoxazolylidene) -ethylidene] -rhodanine.
4. The method of claim 1, in which the dye is l-carboxymethyl 5 (3 methyl 2(3H) thiazolinyl idene)isopropylidene]-3-pheny1-2-thiohydantoin.
5. The method of claim 1, in which the dye is 3-carboxymethyl 5 [(3 methyl 2(3H) thiazolylidene) isopropylidene]-rhodanine.
References Cited in the file of this patent UNITED STATES PATENTS 2,078,233 Brooker Apr. 27, 1937 2,263,757 1 Brooker et al. Nov. 25, 1941 2,282,116 Brooker May 5, 1942 OTHER REFERENCES Mees, Theory of the Photographic Process, pages 254-257, published by Macmillan Co., New York, 1942.

Claims (1)

1. THE METHOD OF OBTAINING A DIRECT-POSITIVE IMAGE IN A SILVER HALIDE EMULSION LAYER, WHICH COMPRISED IMAGEWISE EXPOSING TO A HIGH INTENSITY SHORT DURATION FLASH OF SUFFICIENT INTENSITY AND SUFFICIENTLY SHORT DURATION TO PRODUCE A CLAYDEN DESENSITATIZATION A SILVER HALIDE EMULSION WHICH WHEN EXPOSED UNDER A STEP TABLE HAVING 28 STEPS STARTING WITH APPROXIMATELY ZERO DENSITY AND INCREASING IN INTERVALS OF 0.3 DENSITY, TO A LIGHT FROM A HIGH INTENSITY FLASH LAMP HAVING 18.000 LUMEN SECONDS OUTPUT IN .0005 SECOND, TO FEET FROM THE EMULSION, AND AGAIN EXPOSED WITH THE STEP TABLET ROTATED 90*, TO LOW INTENSITY LIGHT FROM A 1000 WATT TUNGSTEN LAMP 2 FEET FROM THE EMULSION FOR 2 MINUTES, SHOWS AT LEAST 0.10 LOG E DECREASE IN DENSITY BETWEEN AN AREA RECEIVING ONLY LOW INTENSITY EXPOSURE AND AN AREA RECEIVING THE SAME LEVEL OF LOW IN TENSITY EXPOSURE PLUS SOME LEVEL OF IGH INTENSITY EXPOSURE, WHEN DEVELOPED FOR 2 1/4 MINUTES AT 68*F. IN A DEVELOPER OF THE FOLLOWING COMPOSITION:
US440283A 1954-06-29 1954-06-29 Method of increasing clayden desensitization of photographic emulsions Expired - Lifetime US2828203A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
BE539345D BE539345A (en) 1954-06-29
US440283A US2828203A (en) 1954-06-29 1954-06-29 Method of increasing clayden desensitization of photographic emulsions
GB17105/55A GB773388A (en) 1954-06-29 1955-06-14 Method of obtaining a direct-positive image in a silver halide emulsion layer
DEE10923A DE1022090B (en) 1954-06-29 1955-06-27 Process for generating a direct positive image in a halogen silver emulsion utilizing the clay desensitization effect
FR1126802D FR1126802A (en) 1954-06-29 1955-06-29 Method for obtaining positive photographic images directly

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3063350A (en) * 1958-08-11 1962-11-13 Honeywell Regulator Co Recorder
US3765900A (en) * 1970-02-17 1973-10-16 Agfa Gevaert Nv Spectrally sensitized silver halide emulsions

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2078233A (en) * 1934-09-14 1937-04-27 Eastman Kodak Co Photographic emulsion
US2263757A (en) * 1937-12-16 1941-11-25 Eastman Kodak Co Ketone dye and process for preparing it
US2282116A (en) * 1939-04-14 1942-05-05 Eastman Kodak Co Photographic element

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2078233A (en) * 1934-09-14 1937-04-27 Eastman Kodak Co Photographic emulsion
US2263757A (en) * 1937-12-16 1941-11-25 Eastman Kodak Co Ketone dye and process for preparing it
US2282116A (en) * 1939-04-14 1942-05-05 Eastman Kodak Co Photographic element

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3063350A (en) * 1958-08-11 1962-11-13 Honeywell Regulator Co Recorder
US3765900A (en) * 1970-02-17 1973-10-16 Agfa Gevaert Nv Spectrally sensitized silver halide emulsions

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GB773388A (en) 1957-04-24
BE539345A (en)
DE1022090B (en) 1958-01-02

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