催化作用
选择性
丁醇
化学
双金属片
合金
离子半径
无机化学
乙醇
材料科学
化学工程
有机化学
工程类
离子
作者
Zhinuo Wang,Ming Yin,Jifeng Pang,Xianquan Li,Yanan Xing,Yang Su,Shimin Liu,Xiaoyan Liu,Pengfei Wu,Mingyuan Zheng,Tao Zhang
标识
DOI:10.1016/j.jechem.2022.04.049
摘要
Upgrading ethanol to n-butanol is an attractive way for renewable n-butanol production. Herein, Cu was selected to modify NiMgAlO catalysts for improving ethanol conversion and n-butanol selectivity. Over the optimized 2%Cu-NiMgAlO catalyst, ethanol conversion and n-butanol selectivity were enhanced to 30.0% and 64.2%, respectively, in 200 h time on stream at 523 K. According to physicochemical characterizations and theoretical calculations, the key role of multiple active sites in this reaction was extensively investigated. The plate-like structure of hydrotalcite was maintained over 2%Cu-NiMgAlO catalysts, with an average Ni particle size of ca. 5.4 nm. The presence of Cu species created CuNi alloy sites and Lewis acid-base pairs, and increased hydrogen transfer and condensation reactions, resulting in elevated ethanol conversion and n-butanol selectivity. Additionally, CuNi alloy had a strong interaction with CuNiMgAl oxides, forming homogeneous boundary due to their close ionic radius and lattice matching, and afforded the long time stability in the ethanol to n-butanol reaction.
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