TY - JOUR
T1 - On the deactivation of alkali solid catalysts for the synthesis of glycerol carbonate from glycerol and dimethyl carbonate
AU - Li, Jiabo
AU - Wang, Tao
PY - 2011/2
Y1 - 2011/2
N2 - The deactivation of alkali solid catalysts for the synthesis of glycerol carbonate from glycerol and dimethyl carbonate was investigated. Calcium oxide, calcium hydroxide and calcium methoxide were chosen as the representatives of the alkali solid catalysts. When the catalysts were recycled, the yield of glycerol carbonate decreased dramatically. The alkali solid catalyst was converted to the basic calcium carbonate Cax(OH)y(CO 3)z, which was the cause of the decrease of glycerol carbonate yield. It was found that the chemical interactions of the alkali solid catalyst with glycerol and glycerol carbonate led to the formation of the basic calcium carbonate Cax(OH)y(CO3)z, for which the mechanism was proposed. Based on the deactivation mechanism, calcium diglyceroxide was adopted as a new catalyst for the transesterification of glycerol and dimethyl carbonate. Compared to calcium oxide, calcium hydroxide and calcium methoxide, calcium diglyceroxide showed excellent reusability for the transesterification of glycerol and dimethyl carbonate. For calcium oxide, calcium methoxide and calcium diglyceroxide, there were dissolution losses of the catalysts in the reaction medium. For calcium hydroxide, the catalyst dissolution loss in the reaction medium was nearly negligible. For calcium diglyceroxide, the dissolution of the catalyst in the reaction medium did not influence the yield of glycerol carbonate significantly.
AB - The deactivation of alkali solid catalysts for the synthesis of glycerol carbonate from glycerol and dimethyl carbonate was investigated. Calcium oxide, calcium hydroxide and calcium methoxide were chosen as the representatives of the alkali solid catalysts. When the catalysts were recycled, the yield of glycerol carbonate decreased dramatically. The alkali solid catalyst was converted to the basic calcium carbonate Cax(OH)y(CO 3)z, which was the cause of the decrease of glycerol carbonate yield. It was found that the chemical interactions of the alkali solid catalyst with glycerol and glycerol carbonate led to the formation of the basic calcium carbonate Cax(OH)y(CO3)z, for which the mechanism was proposed. Based on the deactivation mechanism, calcium diglyceroxide was adopted as a new catalyst for the transesterification of glycerol and dimethyl carbonate. Compared to calcium oxide, calcium hydroxide and calcium methoxide, calcium diglyceroxide showed excellent reusability for the transesterification of glycerol and dimethyl carbonate. For calcium oxide, calcium methoxide and calcium diglyceroxide, there were dissolution losses of the catalysts in the reaction medium. For calcium hydroxide, the catalyst dissolution loss in the reaction medium was nearly negligible. For calcium diglyceroxide, the dissolution of the catalyst in the reaction medium did not influence the yield of glycerol carbonate significantly.
KW - Alkali solid catalyst
KW - Deactivation
KW - Dimethyl carbonate
KW - Glycerol
KW - Glycerol carbonate
UR - http://www.scopus.com/inward/record.url?scp=79551687270&partnerID=8YFLogxK
U2 - 10.1007/s11144-010-0259-y
DO - 10.1007/s11144-010-0259-y
M3 - Article
AN - SCOPUS:79551687270
SN - 1878-5190
VL - 102
SP - 113
EP - 126
JO - Reaction Kinetics, Mechanisms and Catalysis
JF - Reaction Kinetics, Mechanisms and Catalysis
IS - 1
ER -