Selective Conversion of Ethanol and Acetaldehyde to 1,3-Butadiene Over Zr-HMS Catalysts

被引:1
作者
Li, Shuying [1 ,2 ]
Huang, Bin [1 ]
Jin, Changzi [1 ]
Wang, Rui [1 ]
Jiang, Heng [1 ]
Yang, Guang-Sheng [2 ]
Huang, Shengjun [3 ]
机构
[1] Liaoning Petrochem Univ, Sch Petrochem Engn, Fushun 113001, Peoples R China
[2] Liaoning Normal Univ, Sch Chem & Chem Engn, Dalian 116029, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, Div Fossil Energy Convers, Dalian 116023, Peoples R China
基金
中国国家自然科学基金;
关键词
Ethanol; Acetaldehyde; 1; 3-Butadiene; Zr-HMS; Reaction mechanism; BUTADIENE; SITES; BIOETHANOL;
D O I
10.1007/s10563-023-09390-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The conversion of ethanol and acetaldehyde to 1,3-butadiene has been an emerging process to produce key chemicals. The preparation of highly efficient catalysts and the understanding of reaction mechanism are current research priority. Herein, mesoporous silica framework confining zirconia (Zr-HMS) was prepared and act as catalyst for 1,3-butadiene production from ethanol and acetaldehyde. The prepared catalysts were characterized by Low-angle X-ray powder diffraction, transmission electron microscopy, N-2 physical adsorption-desorption, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy and UV-vis spectra. It has been shown that the Zr-HMS exhibits similar textural properties to supported catalyst (ZrO2/HMS). However, regardless of their comparable activities, higher 1,3-butadiene selectivity is obtained over Zr-HMS, which can be due to the different active zirconia species in two catalysts. Mesoporous framework confining character of Zr-HMS can achieve uniformly dispersed zirconia species. Further investigation toward the reaction process has presented new viewpoints for formation and consumption of some typical intermediates and byproducts, which will help to understand the reaction mechanism and construct efficient catalysts for conversion of ethanol and acetaldehyde to 1,3-butadiene.
引用
收藏
页码:207 / 216
页数:10
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