TY - JOUR
T1 - Promotion effect of coexistent hydromagnesite in a highly active solid base hydrotalcite catalyst for transesterifications of glycols into cyclic carbonates
AU - Kumar, Amit
AU - Iwatani, Ken
AU - Nishimura, Shun
AU - Takagaki, Atsushi
AU - Ebitani, Kohki
N1 - Funding Information:
The work was supported by a Grant-in-Aid for Scientific Research (C) (no. 22560764 ) of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan . A. K. thanks to Delhi University and JAIST for the M. Tech dual degree program.
PY - 2012/5/20
Y1 - 2012/5/20
N2 - Mg-Al hydrotalcites (HTs) prepared with a co-precipitation method in the different conditions were examined for the selective synthesis of carbonates via transesterification of glycols including glycerol, propylene glycol and ethylene glycol. The prepared HT aged for 18 h exhibited a significant catalytic activity over the reaction. XRD and nitrogen adsorption measurements indicate the formation of the hydromagnesite (HM) possessing a high surface area after aging, however, the HM itself is inactive for the reaction. Additionally, progress of the reaction suggests the HT involving HM (HT-HM) shows a gradual increase of glycerol carbonate yield following large uptake of glycerol. The catalyst exhibited a significant catalytic activity in the reaction under the low concentration of glycerol. Therefore, we concluded that the HT-HM acts as a highly active solid base catalyst for the selective synthesis of carbonates via transesterification since the coexistent HM increased the catalytic activity by increasing both surface area and adsorption sites for substrate during the reaction.
AB - Mg-Al hydrotalcites (HTs) prepared with a co-precipitation method in the different conditions were examined for the selective synthesis of carbonates via transesterification of glycols including glycerol, propylene glycol and ethylene glycol. The prepared HT aged for 18 h exhibited a significant catalytic activity over the reaction. XRD and nitrogen adsorption measurements indicate the formation of the hydromagnesite (HM) possessing a high surface area after aging, however, the HM itself is inactive for the reaction. Additionally, progress of the reaction suggests the HT involving HM (HT-HM) shows a gradual increase of glycerol carbonate yield following large uptake of glycerol. The catalyst exhibited a significant catalytic activity in the reaction under the low concentration of glycerol. Therefore, we concluded that the HT-HM acts as a highly active solid base catalyst for the selective synthesis of carbonates via transesterification since the coexistent HM increased the catalytic activity by increasing both surface area and adsorption sites for substrate during the reaction.
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U2 - 10.1016/j.cattod.2011.08.016
DO - 10.1016/j.cattod.2011.08.016
M3 - Article
AN - SCOPUS:84860215874
SN - 0920-5861
VL - 185
SP - 241
EP - 246
JO - Catalysis Today
JF - Catalysis Today
IS - 1
ER -