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Reaction Kinetics, Mechanisms and Catalysis

, Volume 128, Issue 2, pp 763–778 | Cite as

Monodisperse mesoporous La2O3 flakes for the synthesis of glycerol carbonate by efficiently catalyzing the transesterification of dimethyl carbonate with glycerol

  • Chengguang Yue
  • Mingming Fan
  • Pingbo ZhangEmail author
  • Lihua Liu
  • Pingping Jiang
Article
  • 84 Downloads

Abstract

Monodisperse mesoporous La2O3 flakes were prepared by hydrothermal methods using polyethylene glycol as pore-expanding agent, the catalyst exhibited better catalytic activity than normal La2O3 in the reaction of glycerol and dimethyl carbonate to produce glycerol carbonate. The influence of the molecular weight of polyethylene glycol and the mass ratio of La(NO3)3·6H2O/polyethylene glycol on the catalyst was investigated. The results showed that the morphology of La2O3 was remolded to porous flakes interestingly by the suitable type and dosage of pore-expanding agent, this change made the La2O3 catalyst particles have higher alkalinity, better crystallinity, larger specific surface area and good dispersion, which greatly improved the catalytic performance of the catalyst. In addition, the optimal reaction conditions were studied. As a result, the as-prepared porous La2O3 modified by polyethylene glycol-20000 showed excellent catalytic performance with high glycerol carbonate yield of 99.4% under the optimal reaction conditions as follows: the glycerol/dimethyl carbonate molar ratio was 1:5, the catalyst dosage was 5.0 wt% to glycerol, the reaction temperature was 85 °C and the reaction time was 0.5 h. The catalyst had outstanding stability after six cycle reactions with almost no loss of catalytic activity. Thereby, the catalyst was considered to possess the promising potential in industrial production for catalyzing glycerol to the high value-added chemical glycerol carbonate.

Keywords

Lanthanum oxide Polyethylene glycol Glycerol Glycerol carbonate Dimethyl carbonate 

Notes

Acknowledgements

The financial supports from the National Natural Science Foundation of China (NSFC) (No. 21306063), the Fundamental Research Funds for the Central Universities (JUSRP51623A), the Key Research and Development Program of Jiangsu Province (Industry Outlook and Common Key Technologies) (BE2015204), the Fundamental Research Funds for the Central Universities (JUSRP51507), International Joint Research Laboratory for Biomass Conversion Technology at Jiangnan University and MOE & SAFEA for the 111 Project (B13025) are gratefully acknowledged.

Supplementary material

11144_2019_1635_MOESM1_ESM.doc (162 kb)
Supplementary material 1 (DOC 162 kb)

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Copyright information

© Akadémiai Kiadó, Budapest, Hungary 2019

Authors and Affiliations

  • Chengguang Yue
    • 1
  • Mingming Fan
    • 1
  • Pingbo Zhang
    • 1
    Email author
  • Lihua Liu
    • 1
  • Pingping Jiang
    • 1
  1. 1.Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material EngineeringJiangnan UniversityWuxiPeople’s Republic of China

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