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Highly Active Nonpromoted Hydrotreating Catalysts through the Controlled Growth of a Supported Hexagonal WS2 Phase

机译:通过负载型六方WS2相的可控生长来制备高活性的非促进型加氢处理催化剂

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摘要

Highly active nonpromoted W-based hydrotreating catalysts are prepared through a molecular approach with a control of each step. This approach yields WS2 crystallites exhibiting hexagonal 2D morphology, which have been characterized by combining XPS and HR HAADF-STEM techniques and ab initio molecular modeling. The first step is the impregnation of a welldefined precursor, [W(OEt)5]2, grafted onto partially dehydroxylated amorphous silica-alumina (ASA) and characterized at the molecular level by spectroscopic techniques (NMR and IR). The use of increasing amounts of W precursor reveals the formation of (i) a layer of tungsten surface species grafted on the surface and (ii) layers of more mobile adsorbed species loosely bonded to the surface. Sulfidation of these materials provides WS2 supported on ASA, which shows unprecedented lower sulfidation temperatures down to ambient temperature and improved activity by comparison with conventional references (polyoxometalate route). In addition, these improved activities are explained not only by a better level of sulfidation but also by the 2D hexagonal-like morphology of WS2 crystallites (revealed by HR HAADFSTEM), in contrast to a truncated triangle-like morphology for conventional samples. This molecular approach thus opens new avenues to understand and improve the performances of hydrotreating catalysts.
机译:通过分子方法在控制每个步骤的情况下制备高活性,无助催化的W基加氢处理催化剂。这种方法产生了具有六角形2D形态的WS2微晶,这些微晶通过结合XPS和HR HAADF-STEM技术以及从头算分子模型进行了表征。第一步是浸渍定义明确的前体[W(OEt)5] 2,将其接枝到部分脱羟基的无定形二氧化硅-氧化铝(ASA)上,并通过光谱技术(NMR和IR)在分子水平上进行表征。使用增加量的W前驱物揭示了(i)嫁接在表面上的一层钨表面物质的形成和(ii)松散地结合到表面上的更多可移动吸附物质的层的形成。这些材料的硫化提供了在ASA上支持的WS2,与常规参考文献(多金属氧酸盐路线)相比,它显示了前所未有的更低的硫化温度,低至环境温度,活性得到改善。此外,这些改进的活性不仅可以通过更好的硫化水平来解释,还可以通过WS2晶体的2D六角形形态(由HR HAADFSTEM揭示)来解释,这与常规样品的截头三角形形态相反。因此,这种分子方法为理解和改善加氢处理催化剂的性能开辟了新途径。

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