GB616132A - Improvements in the production of cellulose derivatives - Google Patents

Improvements in the production of cellulose derivatives

Info

Publication number
GB616132A
GB616132A GB25830/46A GB2583046A GB616132A GB 616132 A GB616132 A GB 616132A GB 25830/46 A GB25830/46 A GB 25830/46A GB 2583046 A GB2583046 A GB 2583046A GB 616132 A GB616132 A GB 616132A
Authority
GB
United Kingdom
Prior art keywords
acetate
ester
parts
cellulose
butyrate
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
GB25830/46A
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.)
Acordis UK Ltd
Original Assignee
British Celanese 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 British Celanese Ltd filed Critical British Celanese Ltd
Publication of GB616132A publication Critical patent/GB616132A/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
    • C08B3/22Post-esterification treatments, including purification

Abstract

A process for the production of cellulose esters of increased acyl content comprises heating a mixture of a partially hydrolysed organic acid ester of cellulose and an organic acid anhydride dissolved in an organic solvent medium free from catalyst. The product is precipitated from solution in fibrous form and is relatively easily washed and dried. It possesses a degree of stability substantially greater than the hydrolysed cellulose ester from which it is prepared. The further esterification may be halted at any point short of the tri-ester. Esters which may be thus prepared include cellulose acetate, propionate, butyrate (including the triacetate, tri-propionate, tri-butyrate) and fully esterified mixed esters such as cellulose acetate-propionate, acetate-butyrate, acetate-stearate, acetate-laurate, acetate-crotonate and butyrate-crotonate. The hydrolysed ester (1 part by weight) may be dissolved in 3-10 parts by weight of organic acid and 0.1 to 2.0 parts of the anhydride added, depending on the degree of esterification desired, and heated from 60 DEG C. to 100 DEG C. or more for 6-200 hours. In an example 10 parts by weight of cellulose acetate of acetyl value 49 per cent (as acetic acid) are dissolved in 40 parts glacial acetic acid and 5 parts acetic anhydride added. Reaction is allowed to take place at 70 DEG C. for 24 hours. The ester is precipitated by addition of water, and has an acetyl value of 54.9 per cent.
GB25830/46A 1945-09-11 1946-08-28 Improvements in the production of cellulose derivatives Expired GB616132A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US616132XA 1945-09-11 1945-09-11

Publications (1)

Publication Number Publication Date
GB616132A true GB616132A (en) 1949-01-17

Family

ID=22036924

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25830/46A Expired GB616132A (en) 1945-09-11 1946-08-28 Improvements in the production of cellulose derivatives

Country Status (1)

Country Link
GB (1) GB616132A (en)

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