US2756148A - Photographic emulsion having clayden effect susceptibility - Google Patents

Photographic emulsion having clayden effect susceptibility Download PDF

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Publication number
US2756148A
US2756148A US440282A US44028254A US2756148A US 2756148 A US2756148 A US 2756148A US 440282 A US440282 A US 440282A US 44028254 A US44028254 A US 44028254A US 2756148 A US2756148 A US 2756148A
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US
United States
Prior art keywords
emulsion
bromide
clayden
addition
minutes
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US440282A
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English (en)
Inventor
Edgar A Macwilliam
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to BE539322D priority Critical patent/BE539322A/xx
Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co
Priority to US440282A priority patent/US2756148A/en
Priority to GB17104/55A priority patent/GB777181A/en
Priority to DEE10861A priority patent/DE1008570B/de
Priority to FR1126711D priority patent/FR1126711A/fr
Application granted granted Critical
Publication of US2756148A publication Critical patent/US2756148A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/015Apparatus or processes for the preparation of emulsions

Definitions

  • This invention relates to photography and particularly to a method of making a photographic emulsion which shows high susceptibility to the Clayden effect.
  • Clayden effeet The feature which characterizes the Clayden effeet is that the initial exposure of short duration to relatively high intensity light desensitizes the emulsion so that subsequent exposure to weak intensity light produces less effect than if the pro-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 on making it appear that the effect is a reversal.
  • the elfect known as the Clayden effect has a number of practical applications. Yule and Maurer have described in their application Serial No. 291,623, now U. S. Patent No. 2,691,586, use of the Clayden eifect in preparing a pro-screened photographic material with which halftone negatives may be prepared-from a continuous tone positive without the use of the conventional halftone screen.
  • the usefulness of such pro-screened 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 effect.
  • the susceptibiilty of the emulsion to the Clayden effect is increased.
  • a gelatin solution of an alkali metal chloride and an alkali metal bromide is first prepared, in whichthe solution contains more than about one-half molar proportion of the alkali metal chloride and less than 0.1 molar proportion of the alkali metal bromide.
  • the alkali metal halides customarily used are the sodium, potassium or ammonium salts.
  • the concentration of alkali metal halide in the gelatin may vary considerably; however, the range from 0.4 gram to 3.0 grams of alkali metal halide per gram of gelatin has been found to give satisfactory results.
  • the precipitation of the silver halide should be carried out at a temperature of from 50 to C. in order to obtain the enhanced Clayden effect susceptibility.
  • a temperature of approximately 70 C. is preferred.
  • the emulsion may be sensitized with an optical sensitizing dye of the merocyanine or hemioxonol class as described in my application Serial No. 440,283, filed concurrently herewith, and this also increases the Clayden efiect susceptibility.
  • Example 1 A solution of grams of silver nitrate in 65000. of distilled water at 60 C. was added during 6 /3 minutes to a solution of 50 grams of gelatin, 42 grams of sodium chloride and 1.75 grams of potassium bromide in 1287 cc. of distilled water at 71 C. Four and one-quarter minutes after the commencement of the silver nitrate addition, the additionof a solution of 37 grams of potassium bromide in 127 cc. of distilled waterat 40 C. was begun and continued for the remaining two minutes of the silver run. The resulting emulsion was stirred for '10 minute s at 71 C. before the addition of 25 grams of dry gelatin soaked in water. The emulsion was stirred a further four minutes at 71 C.
  • the emulsion was sensitized with a sulfur sensitizer such as disclosed in Sheppard U. S. Patent 1,574,944 to its maximum contrast. A further portion of 86grams of gelatin was then added and stirred until it was dispersed. Before coating there was mixed with the emulsion from 0.1 to 0.2 gram of l'carboxymethyl-5-[(3-ethy1'2-( 1)- benzotxazolylidene)--ethylidene]-3-phenyl-2-thiohydantoin dissolved in 1% alcoholic'tiethylamine solution.
  • a sulfur sensitizer such as disclosed in Sheppard U. S. Patent 1,574,944
  • Example 3 Three chlorobromide emulsions were made as described in Example 1 exceptthat the second potassium bromide solution was added during the last six minutes, the last four minutes and the last two minutes, respectively, of the silver nitrate run, so that the silver and bromide runs ended at approximately the same time.
  • susceptibility to Clayden elfect was found to be increased as "more of the additional potassium bromide was added during the latter part of the run, as shown in the following table:
  • What I claim is: 1. The method of making a photographic emulsion having a high susceptibility to, Clayden desensitization,

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Colloid Chemistry (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
US440282A 1954-06-29 1954-06-29 Photographic emulsion having clayden effect susceptibility Expired - Lifetime US2756148A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
BE539322D BE539322A (fr) 1954-06-29
US440282A US2756148A (en) 1954-06-29 1954-06-29 Photographic emulsion having clayden effect susceptibility
GB17104/55A GB777181A (en) 1954-06-29 1955-06-14 Improvements in photographic sensitive materials
DEE10861A DE1008570B (de) 1954-06-29 1955-06-14 Verfahren zur Herstellung einer photographischen Emulsion
FR1126711D FR1126711A (fr) 1954-06-29 1955-06-25 émulsions photographiques sensibles à l'effet clayden

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US440282A US2756148A (en) 1954-06-29 1954-06-29 Photographic emulsion having clayden effect susceptibility

Publications (1)

Publication Number Publication Date
US2756148A true US2756148A (en) 1956-07-24

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
US440282A Expired - Lifetime US2756148A (en) 1954-06-29 1954-06-29 Photographic emulsion having clayden effect susceptibility

Country Status (5)

Country Link
US (1) US2756148A (fr)
BE (1) BE539322A (fr)
DE (1) DE1008570B (fr)
FR (1) FR1126711A (fr)
GB (1) GB777181A (fr)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3030209A (en) * 1958-07-02 1962-04-17 Eastman Kodak Co High-contrast photographic silver chloride emulsions and method of processing
US3128180A (en) * 1958-07-02 1964-04-07 Eastman Kodak Co Hardened high-contrast photographic silver chloride emulsions and method of processing
US3189456A (en) * 1961-06-19 1965-06-15 Du Pont Radiation-sensitive emulsions and elements and their preparation
US3201250A (en) * 1959-01-12 1965-08-17 Eastman Kodak Co Dimensionally stable gelatincontaining film product
US3364026A (en) * 1963-02-14 1968-01-16 Eastman Kodak Co Fogged silver halide direct positive solarizing elements containing merocyanine dyes
US3477852A (en) * 1965-11-08 1969-11-11 Eastman Kodak Co Direct-positive silver halide emulsion resistant to kink-marking desensitization
US3482982A (en) * 1965-09-22 1969-12-09 Fuji Photo Film Co Ltd Process for producing silver iodobromide photographic emulsion
DE2112729A1 (de) * 1970-03-20 1971-09-30 Eastman Kodak Co Farbphotographisches Aufzeichnungsmaterial
WO1983002174A1 (fr) * 1981-12-19 1983-06-23 Takiguchi, Hideki Procede de preparation d'une emulsion d'halogenure d'argent

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR545944A (fr) * 1922-01-16 1922-10-24 émulsion sensible pour applications photographiques et son procédé de préparation
US1574944A (en) * 1924-06-06 1926-03-02 Eastman Kodak Co Photographic light-sensitive material and process of making the same
GB580173A (en) * 1943-03-15 1946-08-29 Kodak Ltd Improvements in or relating to photographic processes
GB690997A (en) * 1949-07-04 1953-05-06 Bayer Ag Process and photographic material for the direct production of positive photographic images

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR545944A (fr) * 1922-01-16 1922-10-24 émulsion sensible pour applications photographiques et son procédé de préparation
US1574944A (en) * 1924-06-06 1926-03-02 Eastman Kodak Co Photographic light-sensitive material and process of making the same
GB580173A (en) * 1943-03-15 1946-08-29 Kodak Ltd Improvements in or relating to photographic processes
GB690997A (en) * 1949-07-04 1953-05-06 Bayer Ag Process and photographic material for the direct production of positive photographic images

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3030209A (en) * 1958-07-02 1962-04-17 Eastman Kodak Co High-contrast photographic silver chloride emulsions and method of processing
US3128180A (en) * 1958-07-02 1964-04-07 Eastman Kodak Co Hardened high-contrast photographic silver chloride emulsions and method of processing
US3201250A (en) * 1959-01-12 1965-08-17 Eastman Kodak Co Dimensionally stable gelatincontaining film product
US3189456A (en) * 1961-06-19 1965-06-15 Du Pont Radiation-sensitive emulsions and elements and their preparation
US3364026A (en) * 1963-02-14 1968-01-16 Eastman Kodak Co Fogged silver halide direct positive solarizing elements containing merocyanine dyes
US3482982A (en) * 1965-09-22 1969-12-09 Fuji Photo Film Co Ltd Process for producing silver iodobromide photographic emulsion
US3477852A (en) * 1965-11-08 1969-11-11 Eastman Kodak Co Direct-positive silver halide emulsion resistant to kink-marking desensitization
DE2112729A1 (de) * 1970-03-20 1971-09-30 Eastman Kodak Co Farbphotographisches Aufzeichnungsmaterial
WO1983002174A1 (fr) * 1981-12-19 1983-06-23 Takiguchi, Hideki Procede de preparation d'une emulsion d'halogenure d'argent

Also Published As

Publication number Publication date
GB777181A (en) 1957-06-19
DE1008570B (de) 1957-05-16
FR1126711A (fr) 1956-11-29
BE539322A (fr)

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