GB337366A - Process for the manufacture of cellulose fatty acid esters - Google Patents

Process for the manufacture of cellulose fatty acid esters

Info

Publication number
GB337366A
GB337366A GB2292329A GB2292329A GB337366A GB 337366 A GB337366 A GB 337366A GB 2292329 A GB2292329 A GB 2292329A GB 2292329 A GB2292329 A GB 2292329A GB 337366 A GB337366 A GB 337366A
Authority
GB
United Kingdom
Prior art keywords
acid
methylene
acetates
cellulose
sulphuric acid
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
GB2292329A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB2292329A priority Critical patent/GB337366A/en
Publication of GB337366A publication Critical patent/GB337366A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B3/00Preparation of cellulose esters of organic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B3/00Preparation of cellulose esters of organic acids
    • C08B3/16Preparation of mixed organic cellulose esters, e.g. cellulose aceto-formate or cellulose aceto-propionate

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

337,366. Carpmael, A., (I. G. Farbenindustrie Akt.-Ges.). July 25, 1929. Cellulose acetates, aceto-propionates, acetobutyrates, &c.-Fatty acid esters of cellulose are produced by carrying out the esterification in the presence of methylene or ethylene chlorides as solvent instead of free acid. By effecting the reaction at temperatures of 20-60‹ C., degradation of the cellulose is avoided and clear solutions of unusual homogeneity and viscosity are obtained which may be spun directly or may be hydrolyzed, e.g. to give acetone solubility. The primary or secondary esters may be precipitated with aqueous or other liquids. The methylene or ethylene chlorides are recovered from the solutions or the precipitated ester by distillation and are returned to the cycle of manufacture. By the use of methylene or ethylene chloride, the quantity of catalyst may be reduced, e.g., 0.5 per cent of sulphuric acid may be employed. The invention is applicable to acetates, propionates, butyrates and mixed esters. Examples are given of the production of acetates from cotton wool and linters by the use of acetate anhydride, methylene or ethylene chloride, and a small quantity of sulphuric acid or sodium bisulphide ; and of aceto-propionates and aceto-butyrates, using acetic anhydride with propionic or butyric acid. Hydrolysis of the primary acetate is effected by addition of 50 per cent of acetic acid and sulphuric acid or of water and hydrochloric or sulphuric acid to give a acetone-soluble acetates which are precipitated with water, washed and dried. When precipitating by the use of non-aqueous liquids, e.g. benzene, the mixture of liquids is worked up by fractional distillation and acetic acid is obtained in concentrated form.
GB2292329A 1929-07-25 1929-07-25 Process for the manufacture of cellulose fatty acid esters Expired GB337366A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2292329A GB337366A (en) 1929-07-25 1929-07-25 Process for the manufacture of cellulose fatty acid esters

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2292329A GB337366A (en) 1929-07-25 1929-07-25 Process for the manufacture of cellulose fatty acid esters

Publications (1)

Publication Number Publication Date
GB337366A true GB337366A (en) 1930-10-27

Family

ID=10187240

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2292329A Expired GB337366A (en) 1929-07-25 1929-07-25 Process for the manufacture of cellulose fatty acid esters

Country Status (1)

Country Link
GB (1) GB337366A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2588051A (en) * 1949-08-09 1952-03-04 Courtaulds Ltd Production of cellulose esters
US2680693A (en) * 1949-08-31 1954-06-08 British Celanese Manufacture of cellulose esters

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2588051A (en) * 1949-08-09 1952-03-04 Courtaulds Ltd Production of cellulose esters
US2680693A (en) * 1949-08-31 1954-06-08 British Celanese Manufacture of cellulose esters

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