GB356665A - - Google Patents

Info

Publication number
GB356665A
GB356665A GB7073/30A GB707330A GB356665A GB 356665 A GB356665 A GB 356665A GB 7073/30 A GB7073/30 A GB 7073/30A GB 707330 A GB707330 A GB 707330A GB 356665 A GB356665 A GB 356665A
Authority
GB
United Kingdom
Prior art keywords
parts
acid
anhydride
cellulose
treating
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
GB7073/30A
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
Publication of GB356665A publication Critical patent/GB356665A/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
    • C08B3/18Aceto-butyrates

Abstract

Carboxylates.-Mixed carbohydrate esters are formed by treating the carbohydrate or a conversion product thereof with a quantity of fatty acid anhydride calculated for the formation of triacidylate in combination with a quantity of a fatty acid different from that corresponding with the anhydride, with or without a catalyst. The products may be hydrolyzed in known manner. The reaction may be carried out in the presence of acetic acid, propionic acid, benzene or the like as a diluent. In examples, (1) a cellulose acetobutyrate is produced by introducing 100 parts of cellulose into a mixture of 100 parts acetic anhydride, 100 parts butyric acid, 600 parts liquid sulphur dioxide and 12 parts of sulphuric acid at a temperature of 18-23 DEG C., followed by addition of 85-90 parts acetic anhydride and completion of the esterification at 23-24 DEG C.; hydrolysis is effected by a mixture of 100 parts 30 per cent butyric acid and 3 parts sulphuric acid: (2) a cellulose butyropropionate is obtained by treating 100 parts cellulose at 40 DEG C. with 245-250 parts of propionic anhydride, 400 parts of butyric acid and 100 parts of zinc chloride: (3) a starch acetobutyrate is obtained by treating 100 parts of starch with 185 parts of acetic anhydride, 150 parts of butyric acid, 400-600 parts of benzene and 3 parts of sulphuric acid in a rotating drum at 40-60 DEG C.; the product is isolated by centrifuging and washed with water and dried; it is soluble in acetone.
GB7073/30A 1929-03-04 1930-03-04 Expired GB356665A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE356665T 1929-03-04

Publications (1)

Publication Number Publication Date
GB356665A true GB356665A (en) 1931-09-10

Family

ID=31895292

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7073/30A Expired GB356665A (en) 1929-03-04 1930-03-04

Country Status (1)

Country Link
GB (1) GB356665A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2462210A (en) * 1945-05-30 1949-02-22 Gen Mills Inc Starch esters

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2462210A (en) * 1945-05-30 1949-02-22 Gen Mills Inc Starch esters

Similar Documents

Publication Publication Date Title
Malm et al. Preparation of cellulose acetate-Action of sulfuric acid
GB356665A (en)
JPH0582841B2 (en)
US2329705A (en) Organic esters of cellulose
US1613451A (en) Process of making acylated cellulose ethers
US2372565A (en) High viscosity cellulose propionate and method of making
US2338587A (en) Method of treating cellulose esters
US1731299A (en) Treatment of cellulose prior to esterification
US1701229A (en) Ucts therefrom
US1857183A (en) Treatment of cellulose preparatory to esterification
GB275641A (en) Process for the production of cellulose esters
US1912189A (en) Manufacture of cellulose butyric esters
US1869307A (en) Treatment of cellulose prior to esterification
GB368271A (en) Manufacture of cellulose derivatives
US2022446A (en) Process of preparing organic cellulose esters
GB301036A (en)
US1829822A (en) Manufacture of cellulose acetate
GB217168A (en) Process for the production of cellulose conversion products
GB321575A (en) Process for the manufacture of cellulose esters
SU24314A1 (en) Acetyl Cellulose Production Method
GB364794A (en) Improved process of acetylating cellulose
GB343655A (en) Improvements in the manufacture of esters of cellulose or of its transformation products or of other carbohydrates
US1655870A (en) Process for the manufacture of cellulose acetate
GB303493A (en) Process for the preparation of sulphuric esters of cellulose
GB400249A (en) Improvements in organic esters of cellulose and method of preparing the same