GB585758A - Improvements in or relating to the production of photographic emulsions - Google Patents

Improvements in or relating to the production of photographic emulsions

Info

Publication number
GB585758A
GB585758A GB21091/44A GB2109144A GB585758A GB 585758 A GB585758 A GB 585758A GB 21091/44 A GB21091/44 A GB 21091/44A GB 2109144 A GB2109144 A GB 2109144A GB 585758 A GB585758 A GB 585758A
Authority
GB
United Kingdom
Prior art keywords
emulsion
acid
added
anion
water
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
Application number
GB21091/44A
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.)
KENNETH GEORGE ALFRED PANKHURS
Original Assignee
KENNETH GEORGE ALFRED PANKHURS
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
Application filed by KENNETH GEORGE ALFRED PANKHURS filed Critical KENNETH GEORGE ALFRED PANKHURS
Priority to GB21091/44A priority Critical patent/GB585758A/en
Priority to US623445A priority patent/US2527261A/en
Priority to FR916615D priority patent/FR916615A/en
Publication of GB585758A publication Critical patent/GB585758A/en
Priority to DEP30274D priority patent/DE825202C/en
Expired legal-status Critical Current

Links

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

Landscapes

  • 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)
  • Compositions Of Macromolecular Compounds (AREA)
  • Photosensitive Polymer And Photoresist Processing (AREA)

Abstract

585,758. Photographic emulsions. HART, J. A. H., PANKHURST, K.'G. A., and SMITH, R. C. M. Oct. 30, 1944, Nos. 21091 and 24778. [Class 98 (ii)] . A photographic emulsion contains a complex of gelatin formed with an anion soap or a sulphonic acid containing a highly hydrophobic anion, the complex containing dispersed silver halide, dispersed in a predominantly organic solvent medium. The emulsion may have incorporated therein a proportion of another colloid which is soluble in the solvent medium already present in the emulsion or which is soluble in a solvent medium which is miscible with the solvent medium already present: The anion soap solution or a solution of the free acid corresponding thereto may be added to a gelatino silver halide emulsion and the gelatin complex allowed to sediment out. The emulsion may have a pH value (e.g. 2.5 to 3.0, or even as low as 2.0) below the isoelectric point of the gelatin, or a higher pH value and contain an electrolyte. A method is described of determining the optimum ratio of the soap to the gelatin which results in a gelatin complex of the highest solubility in organic solvents. The anion of the anion soap should be as hydrophobic as possible, and the electrolyte concentration in the solution should be as low as possible. The emulsion may be used at a pH below the isoelectric point of the gelatin and either the free acid of the anion soap added or the anion soap itself together with sufficient mineral acid to neutralize the cation of the anion soap. Anion soaps specified are soluble salts of (a) long-chain alkyl carboxylic acids, e.g. of fatty acids containing 8 or more carbon, atoms such as oleic, ricinoleic, linoleic, stearic and palmitic acids ; (b) of long-chain alkyl sulphonic acids ; (c) of sulphated higher fatty alcohols, e.g. in which the alkyl group contains at least 8 carbon atoms such as lauryl and oleyl hydrogen sulphates; (d) of sulphated secondary alcohols containing at least 8 carbon atoms in the chain ; (e) of alkylated aromatic sulphuric acids, e.g. alkyl benzene, alkyl naphthalene, and alkylated hydroxydiphenyl sulphonic acids ; and (f) of long-chain alkyl esters of sulphated succinic acid. Alkali metal (sodium or potassium), ammonium, or amine (triethanolamine or cyclohexylamine) salts may be used. The anion may contain an amino residue as in sodium oleoylaminoethanesulphonate. Numerous commercial anion soaps are specified. Sulphonic acids specified are 2 - naphthol - 1 - sulphonic acid, 1 - naphthol - 4 - sulphonic acid, anthraquinone-2-sulphonic acid, Kiton Fast Yellow 3G and Naphthalene Orange GS. The aqueous gelatino silver halide emulsion may have already been washed and digested. The organic solvent may contain hydroxy groups, e.g. methyl or ethyl alcohol, ethylene glycol.monomethyl ether, ethyl lactate, or diacetone alcohol, or may be acetone, methyl ethyl ketone, dioxane, methylene chloride, chloroform, or mesityl oxide, with or without water or methyl alcohol. Esters such as methyl .or butyl acetate, ethers such as diethyl ether, or hydrocarbons such as benzene or toluene may be added. The complex may be swollen in the organic solvent medium and dispersion facilitated by gentle warming. The additional colloid may be a cellulose ester such as cellulose nitrate or acetate or a far-hydrolysed cellulose acetate, a polyvinyl acetate or acetal, a methyl methacrylate polymer or a partially hydrolysed derivative thereof, an alkyd resin, or a interpolymer of maleic acid or anhydride with styrene or methyl methacrylate. In example 1, to a diluted aqueous gelatino silver iodobromide emulsion is added an aqueous solution of " Agral N " (Registered Trade Mark), which is essentially a sodium alkylnaphthalene sulphonate, followed by dilute hydrochloric acid. The precipitated complex is washed, dissolved in warm methyl alcohol, reprecipitated by adding water, and redissolved in warm methyl alcohol. In example 2, ethylene glycol monomethyl ether, a methyl alcohol solution of cellulose nitrate and acetone are successively added to the solution prepared according to example 1, to give an emulsion suitable for spraying on to cellulose nitrate lacquered metal. In example 3, to portions of a diluted digested and stabilized gelatino silver halide emulsion whose pH is adjusted to 3.0 by addition of acid, are added the following anion soaps: sodium dodecyl sulphate, " Gardinol 30 (Registered Trade Mark), " Agral N " (Registered Trade Mark), "Perminal N" (Registered Trade Mark), " Aresklene 375," " Teepol X," " Santomerse D," "Aresket 240 " and " Igepon T " (Registered Trade Marks). The precipitated complexes are washed, dissolved in methyl alcohol, reprecipitated with water, redissolved in methyl alcohol and coated on to glass or other supports. In example 4, Aresket 240 is added to portions of a gelatino silver halide emulsion at different dilutions. In example 5, complexes are formed with the soaps Teepol X and Santomerse D and an emulsion whose pH has been adjusted to 7.3 and to which ammonium nitrate has been added. In example 6, Aresket 240 is added to an emulsion made with an acid-processed gelatin of high isoelectric point whose pH has been adjusted to 6.0, and the pH is maintained at 6.0 by addition of hydrochloric acid. The complexes may also be dissolved in ethyl alcohol or ethylene glycol monomethyl ether. - Sensitizing dyes, sulphur sensitizers such as allyl isothiocyanate, gold salts as in Specification 570,393, stabilizers, anti-fogging agents and other agents for modifying the speed, contrast, graininess, fog level and developed image colour may be added. The emulsions may be prepared in a dry form for later redispersion in the spray-coating of lacquered metal sheets for use in the production of photographic templates by film drying, spray drying, or air drying of the emulsion in the form of a shredded set jelly, or by air-drying of the precipitate obtained by addition to water. In example 7, to a melted gelatino silver halide emulsion are successively added " Celite 204 " (purified diatomaceous earth) dispersed in aqueous gelatin solution, " Teepol X " (Registered Trade Mark) and hydrochloric acid. The precipitate is washed, dissolved in warm methyl alcohol, reprecipitated by adding water, redissolved in warm methyl alcohol, and cellulose nitrate and acetone added. The emulsion is reprecipitated by pouring into water, is shredded, soaked in water, and spread out to dry. In example 8, an emulsion prepared as in example 7 is set to a jelly, shredded into water, washed, drained and dried. The emulsion is reconstituted by allowing to swell in methyl alcohol and melting at 125‹ F. The cellulose nitrate may be omitted and the emulsion reconstituted in water or aqueous alcohol, e.g. by soaking in water containing sufficient sodium bicarbonate to neutralize the acid, and melting at 120‹ F. An emulsion for spraying may be made using the dried emulsion shreds, sodium bicarbonate, water and ethyl alcohol. In the production of silk screen stencils, the emulsion is sprayed on to stretched' silk, dried, exposed, developed in a tanning developer and washed in hot water. The development may be effected in alkaline pyrocatechol, the silk plunged into hot water and the wash-out relief image fixed in an acid fixing bath. The wash-out relief image may be prepared on a separate support and transferred to the silk. For colour photography, the emulsions may contain dyes or dyeintermediates, e.g. colour formers. Colour formers may be included in the original emulsion and precipitated with the complex, or may be added to the final emulsion. By suitable selection of an additional colloid (e.g. cellulose nitrate or a hydrophobic colloid containing acid groups), emulsions of varying degrees of developer-permeability may be made for use in multi-layer material in which the layers are developed separately by adjusting the constitution of the developers, e.g. by adding organic solvents. Colour developers containing different colour formers may be used, The emulsions, which may contain other colloids, e.g. cellulose nitrate or a methyl.methacrylatemethacrylic acid copolymer, may be used in the production of negatives to be printed from while wet. A supercoat of a plain gelatinanion soap complex, as described in Specification 585,759 may be provided. Specification 580,504 also is referred to.
GB21091/44A 1944-10-30 1944-10-30 Improvements in or relating to the production of photographic emulsions Expired GB585758A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
GB21091/44A GB585758A (en) 1944-10-30 1944-10-30 Improvements in or relating to the production of photographic emulsions
US623445A US2527261A (en) 1944-10-30 1945-10-19 Production of photographic silver halide emulsions from gelatinanion soap complexes
FR916615D FR916615A (en) 1944-10-30 1945-10-29 photographic emulsions and their preparation process
DEP30274D DE825202C (en) 1944-10-30 1949-01-01 Photographic emulsions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB21091/44A GB585758A (en) 1944-10-30 1944-10-30 Improvements in or relating to the production of photographic emulsions

Publications (1)

Publication Number Publication Date
GB585758A true GB585758A (en) 1947-02-24

Family

ID=10157056

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21091/44A Expired GB585758A (en) 1944-10-30 1944-10-30 Improvements in or relating to the production of photographic emulsions

Country Status (4)

Country Link
US (1) US2527261A (en)
DE (1) DE825202C (en)
FR (1) FR916615A (en)
GB (1) GB585758A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2618556A (en) * 1947-11-19 1952-11-18 Eastman Kodak Co Process for preparing photographic emulsions
US2624673A (en) * 1948-03-01 1953-01-06 Warren S D Co Photosensitive printing plate having a light-sensitive coating consisting of a nonprotein colloid, a phosphate, and a chromium compound

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2737500A (en) * 1950-11-30 1956-03-06 Monsanto Chemicals Process of precipitating anionic substances and precipitated compositions
US2701238A (en) * 1952-03-11 1955-02-01 Bates Mfg Co Silver protecting cloth and process of making the same
BE556138A (en) * 1956-03-26
US2976150A (en) * 1957-10-16 1961-03-21 Du Pont Preparation of silver halide emulsions
US3201250A (en) * 1959-01-12 1965-08-17 Eastman Kodak Co Dimensionally stable gelatincontaining film product
US3067035A (en) * 1959-04-01 1962-12-04 Du Pont Gelatin-anion soap complex dispersion in polyvinyl alcohol photographic emulsions
US3207603A (en) * 1960-06-09 1965-09-21 Dietzgen Co Eugene Diazotype and blueprint photoprinting materials having a coating of waterinsoluble metallic fatty acid soap thereon
US3335011A (en) * 1962-03-23 1967-08-08 Pavelle Corp Production of stabilized dispersions of color couplers for photographic materials
US3372030A (en) * 1962-12-14 1968-03-05 Pavelle Corp Method of shortening the processing time of color photography
EP4210942A1 (en) * 2020-09-14 2023-07-19 Saint-Gobain Glass France Process for producing a composite pane having a hologram

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1290794A (en) * 1917-05-24 1919-01-07 Eastman Kodak Co Colored photographic element and process of making the same.
US1844716A (en) * 1929-04-19 1932-02-09 Eastman Kodak Co Process of making photographic emulsions
FR831199A (en) * 1934-03-15 1938-08-25 Process for the production of reliefs by dissolution
BE434981A (en) * 1938-06-23
BE440854A (en) * 1939-01-23
GB537256A (en) * 1939-09-13 1941-06-16 Eastman Kodak Co Process employing non-diffusing compounds for use in colour photography and other photographic processes
BE441871A (en) * 1940-07-09
GB556360A (en) * 1942-01-28 1943-10-01 Thomas Thorne Baker Improvements in or relating to photographic processes
GB580504A (en) * 1944-07-04 1946-09-10 Cecil Waller Improvements in or relating to the production of photographic silver halide emulsions

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2618556A (en) * 1947-11-19 1952-11-18 Eastman Kodak Co Process for preparing photographic emulsions
US2624673A (en) * 1948-03-01 1953-01-06 Warren S D Co Photosensitive printing plate having a light-sensitive coating consisting of a nonprotein colloid, a phosphate, and a chromium compound

Also Published As

Publication number Publication date
DE825202C (en) 1951-12-17
FR916615A (en) 1946-12-11
US2527261A (en) 1950-10-24

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