GB679764A - Improvements in or relating to cellulose derivative emulsions - Google Patents

Improvements in or relating to cellulose derivative emulsions

Info

Publication number
GB679764A
GB679764A GB1402950A GB1402950A GB679764A GB 679764 A GB679764 A GB 679764A GB 1402950 A GB1402950 A GB 1402950A GB 1402950 A GB1402950 A GB 1402950A GB 679764 A GB679764 A GB 679764A
Authority
GB
United Kingdom
Prior art keywords
emulsion
water
cellulose acetate
cellulose
mixture
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
GB1402950A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB1402950A priority Critical patent/GB679764A/en
Publication of GB679764A publication Critical patent/GB679764A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L1/00Compositions of cellulose, modified cellulose or cellulose derivatives
    • C08L1/08Cellulose derivatives
    • 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

Abstract

A water-insoluble cellulose ester or ether is formed into an emulsion by adding it in a dry solid condition, preferably in p chips, shreds, or powder form, to a previously made "water-in-oil" type of emulsion, the continuous phase being formed by an organic solvent for the cellulose derivative or a mixture of solvents, with or without plasticizers, the solvents and plasticizers being insoluble or only sparingly soluble in water, and then effecting colloiding, dissolving, and emulsifying of the cellulose derivative in one operation by simple stirring. If desired, the plasticizers may be added to the emulsion subsequently to dissolving and emulsifying the cellulose derivative. The cellulose derivative may be cellulose acetate, propionate, butyrate, stearate, palmitate, or laurate, or it may be ethyl, propyl, butyl, benzyl, hexyl, or ethyl-hexyl cellulose ether. The plasticizer may be tricresyl phosphate, acetophenone, or benzophenone. In an example, nonaethylene glycol oleate is dissolved in water and then a mixture of benzyl alcohol and methylene chloride is added and mixed to form an emulsion. Shredded cellulose acetate film scrap is then mixed with the emulsion. A stable emulsion is formed. If diluted to 1 per cent concentration of cellulose acetate by addition of water it may be changed from a water-in-oil type of emulsion to an oil-in-water type by adding a sulphonated fatty alcohol. In another example gelatine is used as emulsifier. The gelatine is dissolved in water and an emulsion is made by adding a mixture of methylene chloride and benzyl alcohol and stirring. Shredded cellulose acetate is added, and stirring is continued till an emulsion of the cellulose acetate is obtained. An emulsion in the form of a thick cream is obtained. Silver bromide and other light-sensitive salts may be incorporated in the production of a photographic emulsion. The emulsion may be used in the production of films. Instead of gelatine, gums or alginates may be used. In another example, nonaethylene glycol oleate and a sulphonated fatty alcohol are dissolved in water rendered alkaline with potassium carbonate. The solution is poured into a mixture of methylene chloride, benzyl alcohol and benzophenone, and the mixture is stirred until an emulsion is formed. Shredded cellulose acetate is added and stirring is continued till the cellulose acetate is dissolved and emulsified. A creamy emulsion is obtained. Emulsions in acid, neutral, or alkaline condition may be obtained. They may be applied to paper, cloth, leather, rope, walls or floors, by dipping, rubbing, spreading by knife or roller or by other methods.
GB1402950A 1950-06-05 1950-06-05 Improvements in or relating to cellulose derivative emulsions Expired GB679764A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1402950A GB679764A (en) 1950-06-05 1950-06-05 Improvements in or relating to cellulose derivative emulsions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1402950A GB679764A (en) 1950-06-05 1950-06-05 Improvements in or relating to cellulose derivative emulsions

Publications (1)

Publication Number Publication Date
GB679764A true GB679764A (en) 1952-09-24

Family

ID=10033701

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1402950A Expired GB679764A (en) 1950-06-05 1950-06-05 Improvements in or relating to cellulose derivative emulsions

Country Status (1)

Country Link
GB (1) GB679764A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4663077A (en) * 1984-06-11 1987-05-05 Morton Thiokol Inc. Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein
US4683080A (en) * 1984-06-11 1987-07-28 Morton Thiokol, Inc. Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4663077A (en) * 1984-06-11 1987-05-05 Morton Thiokol Inc. Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein
US4683080A (en) * 1984-06-11 1987-07-28 Morton Thiokol, Inc. Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein

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