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首页> 外文期刊>ACS catalysis >Structure-Activity Correlations in Hydrodesulfurization Reactions over Ni-Promoted MoxW(1-x)/Al2O3 Catalysts
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Structure-Activity Correlations in Hydrodesulfurization Reactions over Ni-Promoted MoxW(1-x)/Al2O3 Catalysts

机译:Ni促进的MoxW(1-x)/ Al2O3催化剂加氢脱硫反应的结构活性相关性

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In this work, we have investigated the activation process and structure of Ni-promoted MoxW(1-x)S2/Al2O3 hydrodesulfurization (HDS) catalysts. Conversion of Mo and W oxides to the catalytically active MS, (M = Mo, W) phase by sulfidation in gaseous H2S/1-12 proceeded via different pathways, as found by XPS and EXAFS. The slower sulfidation kinetics of W on the alumina support formed NiMoxWo_4 sulfides with a two-dimensional core shell structure. Mo was mostly located in the core and W in the shell, as evidenced by EXAFS. Increasing the H2S/H-2 pressure during sulfidation distributed Mo and W more homogeneously in the metal sulfide particles. This was attributed to the more favorable sulfidation of W under these conditions (i.e., below the temperature of MoS, formation). Catalytic testing was consistent with these findings and demonstrated that a core shell structure is the active phase in thiophene HDS (1 atm), whereas a homogeneously mixed MS, phase catalyzes the HDS of dibenzothiophene at 40 bar. This is the first example of a core shell structure in promoted MoxW(l-x)S, catalysts. Support interactions in the oxidic precursor, which affect the sulfidation kinetics, were determined to play a key role in the formation of these structures.
机译:在这项工作中,我们研究了镍促进的MoxW(1-x)S2 / Al2O3加氢脱硫(HDS)催化剂的活化过程和结构。通过XPS和EXAFS发现,通过气态H2S / 1-12中的硫化将Mo和W氧化物转化为催化活性MS(M = Mo,W)相的过程是通过不同的途径进行的。 W在氧化铝载体上的较慢的硫化动力学形成具有二维核壳结构的NiMoxWo_4硫化物。正如EXAFS所证明的,Mo主要位于核心,W位于壳中。硫化过程中H2S / H-2压力的增加使Mo和W在金属硫化物颗粒中分布更均匀。这归因于在这些条件下(即,低于MoS的温度,形成时)W更有利的硫化。催化测试与这些发现一致,并表明核壳结构是噻吩HDS(1 atm)中的活性相,而均匀混合的MS相则在40 bar下催化二苯并噻吩的HDS。这是促进的MoxW(1-x)S催化剂中核壳结构的第一个例子。确定了氧化前体中的载体相互作用会影响硫化动力学,在这些结构的形成中起关键作用。

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