Efficient Promotional Effects of Mo on the Catalytic Hydrogenation of Methyl Acrylate over Ni-Based Catalysts under Mild Conditions

被引:7
|
作者
Sun, Taolue [1 ,2 ]
Wu, Zhenyu [2 ,3 ]
Wang, Gang [2 ,3 ]
Li, Zengxi [1 ,2 ]
Li, Chunshan [2 ]
Wang, Emiang [3 ]
机构
[1] Univ Chinese Acad Sci, Sino Danish Coll, Beijing 100049, Peoples R China
[2] Chinese Acad Sci, Inst Proc Engn Innovat Acad Green Manufacture, Key Lab Multiphase Complex Syst, Beijing Key Lab Ion Liquids Clean Proc, Beijing 100190, Peoples R China
[3] Univ Chinese Acad Sci, Sch Chem Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
NI-MO/AL2O3; CATALYSTS; NI-MO/GAMMA-AL2O3; NI/AL2O3; NICKEL; HYDRODEOXYGENATION; PERFORMANCE; METHANATION; MOLYBDENUM; OIL; NANOPARTICLES;
D O I
10.1021/acs.iecr.1c02447
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A series of Ni/gamma-Al2O3 and Ni-Mo/gamma-Al2O3 catalysts were prepared and evaluated for the hydrogenation of methyl acrylate to methyl propionate in a fixed-bed reactor. Physicochemical characterizations of these catalysts were carried out with Brunauer-Emmett-Teller analysis, X-ray diffraction, UV-vis diffuse reflectance spectroscopy, Raman spectroscopy, hydrogen temperature programed reduction, X-ray photoelectron spectroscopy, and transmission electron microscopy. It was noticed that Mo loaded onto the Ni/gamma-Al2O3 catalyst could not only promote the dispersion of Ni particles but also weaken the interaction between NiO and the gamma-Al2O3 support. The effect of the calcination temperature on Ni-Mo/gamma-Al2O3 catalysts is mainly due to the enhancement of the interaction between Ni species and gamma-Al2O3. The influence of the reduction temperature on the Ni-Mo/gamma-Al2O3 catalysts, as well as the reaction conditions, was also studied in detail. As a result, this hydrogenation process could be efficiently promoted on the optimal 10Ni-10Mo/gamma-Al2O3 catalyst with the highest yield of 94% and selectivity of 99.9%, and no deactivation behavior was observed after 130 h time-on-stream at 100 degrees C and 1.0 MPa.
引用
收藏
页码:152 / 163
页数:12
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