Tuning the base properties of Mg-Al hydrotalcite catalysts using their memory effect

被引:78
作者
Kwon, Dahye [1 ]
Kang, Ji Yeon [1 ]
An, Suna [1 ]
Yang, Inchan [1 ]
Jung, Ji Chul [1 ]
机构
[1] Myongji Univ, Dept Chem Engn, Yongin 17058, South Korea
来源
JOURNAL OF ENERGY CHEMISTRY | 2020年 / 46卷
基金
新加坡国家研究基金会;
关键词
Mg-Al hydrotalcite; Structure; Base properties; Heat treatment; Rehydration; BIODIESEL PRODUCTION; SOYBEAN OIL; BIOMASS; GLUCOSE; ISOMERIZATION; CHEMICALS; CARBONATE; FUELS; OXIDE; TRANSESTERIFICATION;
D O I
10.1016/j.jechem.2019.11.013
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Herein, the relationship between the structure and base properties of Mg-Al hydrotalcite catalysts was comprehensively investigated in relation to heat treatment and rehydration processes, which are well known as memory effects of hydrotalcite. The structure of Mg-Al hydrotalcites changed from layered double hydroxide (LDH) to mixed metal oxide and subsequently to a spinel structure during heat treatment, and it was returned from mixed metal oxide to a LDH structure by rehydration. Based on various characterizations, we successfully proposed a detailed mechanism of memory effect. We also confirmed that the Mg-Al hydrotalcites had weak or strong base sites and that their base properties could be systematically tuned by heat treatment and rehydration. The prepared Mg-Al hydrotalcites were applied to a model reaction, isomerization of glucose to fructose, as base catalysts. Among the catalysts tested, the rehydrated Mg-Al hydrotalcite efficiently produced fructose due to its appropriate base and structure properties. We finally concluded that the base sites of Mg-Al hydrotalcites can be designed as desired by heat treatment and rehydration. Moreover, through systematic design of the base sites of Mg-Al hydrotalcites, these can be promising catalysts for various heterogeneous reactions over base catalysts, giving excellent catalytic performances. (C) 2019 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.
引用
收藏
页码:229 / 236
页数:8
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