GB402733A - Improvement in colloidised mixed cellulose ester products - Google Patents

Improvement in colloidised mixed cellulose ester products

Info

Publication number
GB402733A
GB402733A GB645132A GB645132A GB402733A GB 402733 A GB402733 A GB 402733A GB 645132 A GB645132 A GB 645132A GB 645132 A GB645132 A GB 645132A GB 402733 A GB402733 A GB 402733A
Authority
GB
United Kingdom
Prior art keywords
esters
colloidized
higher fatty
acids
fatty acids
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
GB645132A
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.)
Kodak Ltd
Original Assignee
Kodak Ltd
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 Kodak Ltd filed Critical Kodak Ltd
Priority to GB645132A priority Critical patent/GB402733A/en
Publication of GB402733A publication Critical patent/GB402733A/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
    • C08L1/10Esters of organic acids, i.e. acylates
    • C08L1/14Mixed esters, e.g. cellulose acetate-butyrate

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Treatment And Processing Of Natural Fur Or Leather (AREA)

Abstract

Colloidised cellulosic materials are produced by dissolving a mixed cellulose ester containing less than 4 and more than \ba1/3\be higher fatty acid groups per 24 carbon atoms in the cellulose molecule, and removing the solvent by evaporation. The number of lower fatty acid groups present is preferably less than 11\ba2/3\be and more than 8. As higher fatty acids there are mentioned pelargonic, capric, lauric, myristic, palmitic, stearic, and oleic acids, and as lower fatty acids, acetic, propionic, and butyric acids. There may be present plasticizers, other plastic materials, gums, waxes, heavy metal soaps, higher fatty acids or their esters, resins, or oils. On account of the waterproof properties of the colloidized esters, they are useful for the production of films or sheets for wrapping foodstuffs; as a substitute for rubber in the manufacture of raincoats or the like; for waterproofing surfaces e.g., nitrocellulose lacquer surfaces, for impregnating fabrics, threads, paper, or fabric-insulated wire. The colloidized esters may also be used in the manufacture of lacquers, artificial leather, insulated wires, shatter-proof glass, bottles, or other glassware, knife handles, combs, insulators, cigarette holders, &c. Artificial silk may be produced by spinning a solution of one or several of the mixed esters, either into a hot inert gas, or into a non-solvent.ALSO:Colloidized, cellulosic materials are produced by dissolving a mixed cellulose ester containing less than 4 and more than 1/3 higher fatty acid groups per 24 carbon atoms in the cellulose molecule, and removing the solvent by evaporation. The number of lower fatty acid groups present is preferably less than 112 and more than 8. As higher fatty acids there are mentioned pelargonic, capric, lauric, myristic, palmitic, stearic, and oleic acids, and as lower fatty acids, acetic, propionic, and butyric acids. There may be present plasticizers, other plastic materials, gums, waxes, heavy metal soaps, higher fatty acids or their esters, resins, or oils. On account of the waterproof properties of the colloidized esters, they are useful for the production of films or sheets for wrapping food-stuffs; as a substitute for rubber in the manufacture of raincoats or the like; for impregnating fabrics, threads, paper, or fabric-insulated wire. The colloidized esters may also be used in the manufacture of artificial leather, insulated wires, shatter-proof glass, bottles, or other glassware, knife handles, combs, insulators, cigarette holders, &c.
GB645132A 1932-03-03 1932-03-03 Improvement in colloidised mixed cellulose ester products Expired GB402733A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB645132A GB402733A (en) 1932-03-03 1932-03-03 Improvement in colloidised mixed cellulose ester products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB645132A GB402733A (en) 1932-03-03 1932-03-03 Improvement in colloidised mixed cellulose ester products

Publications (1)

Publication Number Publication Date
GB402733A true GB402733A (en) 1933-12-07

Family

ID=9814707

Family Applications (1)

Application Number Title Priority Date Filing Date
GB645132A Expired GB402733A (en) 1932-03-03 1932-03-03 Improvement in colloidised mixed cellulose ester products

Country Status (1)

Country Link
GB (1) GB402733A (en)

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