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钨负载量对用于甲烷脱氢芳构化的沸石基催化剂活化的影响

Impact of Tungsten Loading on the Activation of Zeolite-Based Catalysts for Methane Dehydroaromatization.

作者信息

Kromwijk Josepha J G, Vloedgraven Job G A, Neijenhuis Fleur, van der Stam Ward, Monai Matteo, Weckhuysen Bert M

机构信息

Inorganic Chemistry and Catalysis Group, Institute for Sustainable and Circular Chemistry, Department of Chemistry, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, Netherlands.

出版信息

ACS Catal. 2025 Apr 18;15(9):7241-7253. doi: 10.1021/acscatal.4c07228. eCollection 2025 May 2.

Abstract

To improve the performance of zeolite-based catalysts for the methane dehydroaromatization (MDA) reaction, it is of importance to understand the nature of the catalytically active phase. Although many studies have been devoted to unraveling the structure of the active site, there is still no consensus. Monomeric, dimeric, and/or clusters of molybdenum oxide or tungsten oxide are proposed precatalyst structures. This precatalyst is activated under reaction conditions, to form (oxy)carbidic species which are believed to be the active site. In this study, we investigated the effect of tungsten dispersion on the activation of W/ZSM-5 catalysts. We observed unexpected long activation times that could be shortened by inert or reductive pretreatment. Based on our investigations, we hypothesize that W/ZSM-5 catalysts with low weight loadings (i.e., 2 wt %) cannot be activated due to the presence of monomeric tungsten. For catalysts with medium weight loadings (i.e., 5 and 7 wt %), restructuring of the tungsten is required for the formation of the active site, which can be achieved through performing a thermal pretreatment. For higher weight loadings (i.e., 10 wt %), reduction plays a key role in the activation of the catalyst. We show that the activation of the catalyst is impacted by the precatalyst structure. These insights aid in the development of suitable activation treatments which could save time and energy if the reaction would be performed at an industrial scale.

摘要

为提高用于甲烷脱氢芳构化(MDA)反应的沸石基催化剂的性能,了解催化活性相的本质很重要。尽管许多研究致力于揭示活性位点的结构,但仍未达成共识。氧化钼或氧化钨的单体、二聚体和/或簇被认为是预催化剂结构。这种预催化剂在反应条件下被活化,形成被认为是活性位点的(氧)碳化物物种。在本研究中,我们研究了钨分散度对W/ZSM-5催化剂活化的影响。我们观察到意想不到的长活化时间,惰性或还原预处理可以缩短该时间。基于我们的研究,我们假设低负载量(即2 wt%)的W/ZSM-5催化剂由于单体钨的存在而无法被活化。对于中等负载量(即5 wt%和7 wt%)的催化剂,形成活性位点需要钨的重构,这可以通过进行热预处理来实现。对于更高的负载量(即10 wt%),还原在催化剂的活化中起关键作用。我们表明催化剂的活化受预催化剂结构的影响。这些见解有助于开发合适的活化处理方法,如果该反应在工业规模上进行,这些方法可以节省时间和能源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22f4/12053828/efdf117c5a68/cs4c07228_0001.jpg

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