加氢脱氧
双金属片
化学
钼
催化作用
镍
氮化物
过渡金属
加氢脱硫
无机化学
有机化学
选择性
图层(电子)
作者
Chenxi Zhao,Jiequan Wang,Xiao Chen,Changhai Liang
标识
DOI:10.1002/ejic.202300073
摘要
Abstract Highly efficient catalysts play an important role in the effective use of biomass oil to produce clean fuel. In this work, pure‐phase Ni−Mo bimetallic nitrides (Ni 2 Mo 3 N and Ni 3 Mo 3 N) with different stoichiometric ratios are prepared by temperature‐programmed nitridation of the metal oxide precursors in ammonia, which are investigated in the hydrodeoxygenation of methyl palmitate in the fixed‐bed reactor at moderate conditions. The physical and chemical properties of catalysts were evaluated by H 2 ‐TPR, XRD, SEM, TEM, XPS, and CO chemisorption. The Ni 2 Mo 3 N catalyst presents the best methyl palmitate hydrogenation activity (con.%=95.4 %) and the maximum hexadecane selectivity (95.0 %), which is obviously higher than those of Ni 3 Mo 3 N and Mo 2 N catalysts. By introducing transition metal Ni into the Mo 2 N lattice to form nickel‐molybdenum bimetallic nitride, the lattice structure and electronic structure of the Mo active center have been changed, which greatly enhances the hydrodeoxygenation performances for the transformation of biomass oil to clean fuel.
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