Abstract

Layered double hydroxides are a promising platform material which can be combined with a variety of active species based on their characteristic features. Silicon@P123-templated Ce-doped layered double hydroxide (SiO2@CeMgAl-LDH(P123)) composites were synthesized via a facile in situ co-precipitation method, and characterized by TEM, X-ray diffraction, FTIR, XPS, CO2-, etc. in detail. Meanwhile, the calcined powder (SiO2@CeMgAl-LDO(P123)) possessed an excellent core–shell structure and a high surface area inherited from the LDH structure, which led to an outstanding catalytic activity (99.7% conversion of propylene oxide, 92.4% selectivity of propylene glycol methyl ether) under mild reaction conditions (120 °C). Cerium oxide provides a large number of oxygen vacancies and significantly improves the medium basic strength of the material, which facilitates the selective ring-opening of PO. Furthermore, the introduction and removal of P123 make the cerium oxide uniformly dispersed on the LDH layers, providing more reaction sites for the reaction of methanol and propylene oxide. The core–shell structure prepared by the in situ co-precipitation method could solve the shortcomings of agglomeration of layered double hydroxides and prolong the catalytic life evidently.

Highlights

  • Low toxicity, high efficiency, and a stable solvent are indispensable features in a green chemical process

  • The obtained material (SiO2@CeMgAl-layered double oxides (LDOs)(P123)) was fully characterized and its catalytic activity was evaluated in the synthesis of Propylene glycol methyl ether (PGME) (Fig. 1)

  • Due to the introduction of P123 and its removal at a high temperature, it can be seen that small CeO2 grains are scattered on the LDO surface, and their average particle sizes are 4 and 4.5 nm, respectively

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Summary

Introduction

High efficiency, and a stable solvent are indispensable features in a green chemical process. The highest conversion and selectivity toward PGME were observed in the presence of materials with mediumstrength basic sites, because high-strength basic sites can lead to a strong stabilization of methoxide and propylene-like species on the surface of the solid.

Results
Conclusion
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