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GB436885A - Improved process for the production of mixed esters of polyhydric alcohols and of carbohydrates - Google Patents

Improved process for the production of mixed esters of polyhydric alcohols and of carbohydrates

Info

Publication number
GB436885A
GB436885A GB11995/34A GB1199534A GB436885A GB 436885 A GB436885 A GB 436885A GB 11995/34 A GB11995/34 A GB 11995/34A GB 1199534 A GB1199534 A GB 1199534A GB 436885 A GB436885 A GB 436885A
Authority
GB
United Kingdom
Prior art keywords
acid
ketene
esterified
cellulose
cotton linters
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
GB11995/34A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and 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
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB436885A publication Critical patent/GB436885A/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
    • C08B3/16Preparation of mixed organic cellulose esters, e.g. cellulose aceto-formate or cellulose aceto-propionate

Landscapes

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

Abstract

Mixed esters of polyhydric alcohols, for example cellulose, are prepared by reacting the polyhydric alcohol with ketene in the presence of one or more organic carboxylic acids in amount substantially in excess of the polyhydric alcohol. Examples of suitable polyhydric alcohols are cotton, wood pulp, low esterified or etherified celluloses, sorbitol, glycerol, glucamine, penta-erythritol, inositol, quebrachitol, starches, and sugars. Organic acids specified are formic, propionic, butyric, valeric, caproic, heptoic, lauric, stearic, oleic, palmitic, erucic, linoleic, pyrivic, levulinic, acrylic, crotonic, isovaleric, benzoic, naphthoic, toluic, furoic, chlorobenzoic, picolinic, phenylacetic, cinnamic, linseed oil acids, chinawood oil acids, cottonseed oil acids, and fatty oil acids generally. The following examples are given: (1) Cotton linters are esterified by means of propionic acid and ketene in presence of sulphuric acid. The primary acetate-propionate may be partially hydrolyzed. (2) Cotton linters are mixed with hydrofluoric acid and n-butyric acid, and ketene is passed into the mixture. The cellulose acetate-n-butyrate may be subjected to hydrolysis. (3) Cotton linters are esterified in a mixture containing hydrofluoric acid, pyruvic acid, and ketene. (4) Cotton linters are esterified by means of propionic acid, coconut oil acids, and ketene in the presence of sulphuric acid. The product may be partially hydrolyzed. (5) Monoethyl cellulose is esterified by means of propionic acid and ketene in the presence of sulphuric acid. (6) Cotton linters are pretreated with formic acid and esterified as in the first example. The reaction may be carried out in the presence of solvent or non-solvent diluents. The cellulose esters may be used in the preparation of coating compositions, films, fibres, and plastics, while the products obtained from polyhydric alcohols are suitable for adhesives and plasticizers, and for use in coating and impregnating compositions. The Specification as open to inspection under Sect. 91 refers also to the treatment of cellulose with a mixture of ketene and nitric acid which has been dehydrated by means of acetic anhydride. This subject-matter does not appear in the Specification as accepted.
GB11995/34A 1933-04-20 1934-04-20 Improved process for the production of mixed esters of polyhydric alcohols and of carbohydrates Expired GB436885A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US436885XA 1933-04-20 1933-04-20

Publications (1)

Publication Number Publication Date
GB436885A true GB436885A (en) 1935-10-21

Family

ID=21928378

Family Applications (1)

Application Number Title Priority Date Filing Date
GB11995/34A Expired GB436885A (en) 1933-04-20 1934-04-20 Improved process for the production of mixed esters of polyhydric alcohols and of carbohydrates

Country Status (1)

Country Link
GB (1) GB436885A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2970513A4 (en) * 2013-03-14 2016-11-30 Celanese Acetate Llc Naturally derived mixed cellulose esters and methods relating thereto

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2970513A4 (en) * 2013-03-14 2016-11-30 Celanese Acetate Llc Naturally derived mixed cellulose esters and methods relating thereto

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