Etherification of glycerol withtert-butyl alcohol catalysed by ion-exchange resins
✍ Scribed by K. Klepáčová; D. Mravec; M. Bajus
- Book ID
- 111490966
- Publisher
- Versita
- Year
- 2006
- Tongue
- English
- Weight
- 286 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0366-6352
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✦ Synopsis
Abstract
The reaction of glycerol with tert-butyl alcohol in the liquid phase on acid Amberlyst-type ion-exchange resins was studied. The influence of temperature, mole ratio n(TBA)/n(G), water and swelling of gel, and macroreticular type of polymer catalysts on etherification reaction was investigated. The most favourable reaction temperature is 75°C. The conversion of glycerol and yield of glycerol tert-butyl ethers has increased with the mole ratio n(TBA)/n(G). Dry form of macroreticular catalysts provided the best results. Etherification reaction of glycerol with isobutylene in non-aqueous conditions gives the highest yield of desired ethers. The influence of water was studied. The gel forms of ion-exchange resins have very low catalytic activity. It can be concluded that water has an inhibition effect on ion-exchange resins. By comparing the gel and macroreticular forms of Amberlyst ion-exchange resins it can be concluded that very acid forms of macroreticular ion-exchange resins with a high degree of crosslinking are more active catalysts for the studied reaction due to their pores which are sufficiently large so that the voluminous tert-butyl ethers of glycerol can be formed. It was estimated that tert-butyl alcohol as tert-butylation agent is not suitable for etherification of glycerol with the formation of di-and triethers.
📜 SIMILAR VOLUMES
Etherification of ethylene and propylene glycols with isobutylene was carried out in the presence of cation exchange resin catalysts, Amberlyst-15, Indion-130, and a homogeneous catalyst, p-toluene sulfonic acid. Kinetics of these reactions was studied in a magnetically stirred 1.0 x 10 -4 m 3 capac