Synthesis of glycerol carbonate from the transesterification of dimethyl carbonate with glycerol using DABCO and DABCO-anchored Merrifield resin

Authors
Simanjuntak, Fidelis Stefanus HubertsonChoi, Ji SikLee, GunukLee, Hye JeongLee, Sang DeukCheong, MinserkKim, Hoon SikLee, Hyunjoo
Issue Date
2015-04
Publisher
ELSEVIER SCIENCE BV
Citation
APPLIED CATALYSIS B-ENVIRONMENTAL, v.165, pp.642 - 650
Abstract
Both DABCO (1,4-diazabicyclo[2.2.2]octane) and Merrifield resin-anchored DABCO ([p-DABCO]Cl), prepared from the reaction of DABCO and Merrifield resin, were found to exhibit high activities for the transesterification of dimethyl carbonate (DMC) with glycerol to produce glycerol carbonate (GLC). FT-IR and NMR spectroscopic results suggest that such a high transesterification activity of DABCO could be attributed to its superior ability to activate glycerol via a strong hydrogen bond formation between a hydroxyl group of glycerol and an amino group of DABCO. Meanwhile, the activation of glycerol by [p-DABCO]Cl proceeds mainly through the hydrogen bond interaction between a hydroxyl group or groups of glycerol and Cl- of [p-DABCO]Cl. The catalytic activity of [p-DABCO]Cl was maintained up to 5 reuses, demonstrating that [p-DABCO]Cl could be used as a recyclable heterogeneous catalyst. (C) 2014 Elsevier B.V. All rights reserved.
Keywords
HETEROGENEOUS CATALYST; HIGHLY EFFICIENT; IONIC LIQUIDS; DIOXIDE; HETEROGENEOUS CATALYST; HIGHLY EFFICIENT; IONIC LIQUIDS; DIOXIDE; Glycerol; Dimethyl carbonate; Glycerol carbonate; Immobilization; DABCO
ISSN
0926-3373
URI
https://pubs.kist.re.kr/handle/201004/125635
DOI
10.1016/j.apcatb.2014.10.071
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KIST Article > 2015
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