Bimodal mesoporous AlMCM-41 supported NiMo catalysts for efficient hydrodesulfurization of 4,6-dimethyldibenzothiophene

IF 6.5 1区 化学 Q2 CHEMISTRY, PHYSICAL
Hao Zhang, Qing Zhang, Guang-Ren Qian, Hong Liu, Yang Yue
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Abstract

In this research, a bimodal mesoporous AlMCM-41 (B-AM41) material was prepared and applied to support NiMo catalysts for the hydrodesulfurization (HDS) of 4,6-dimethyldibenzothiophene. Additionally, catalysts supported on smaller and larger single-pore AlMCM-41 (S-AM41 and L-AM41) were also prepared as reference catalysts. Detailed characterizations show that the proportion, stacking degree, and length of the MoS2 active phase on the different catalysts are distinct. As a result, HDS evaluation indicates that the NiMo/B-AM41 catalyst exhibited better catalytic activity with a reaction rate constant of 10.4 × 10−8 mol g−1 s−1 and a turnover frequency of 7.0 × 10−4 s−1, significantly surpassing the S-AM41 and L-AM41 supported catalysts. The superior activity of the NiMo/B-AM41 catalyst can be attributed to a high sulfidation degree that provides sufficient highly dispersed type Ⅱ MoS2 phases with minimal stacking and moderate slab length. Moreover, the bimodal mesoporous structure promotes the diffusion of 4,6-DMDBT and benefits its contact with active sites.

Abstract Image

Abstract Image

用于 4,6-二甲基二苯并噻吩高效加氢脱硫的双峰介孔 AlMCM-41 支承镍钼催化剂
本研究制备了一种双峰介孔 AlMCM-41(B-AM41)材料,并将其应用于 4,6-二甲基二苯并噻吩加氢脱硫 (HDS) 的 NiMo 催化剂支撑。此外,还制备了支撑在较小和较大单孔 AlMCM-41 材料(S-AM41 和 L-AM41)上的催化剂作为参考催化剂。详细表征结果表明,不同催化剂上 MoS2 活性相的比例、堆叠度和长度各不相同。因此,HDS 评估表明,NiMo/B-AM41 催化剂具有更好的催化活性,反应速率常数为 10.4 × 10-8 mol g-1 s-1,翻转频率为 7.0 × 10-4 s-1,明显超过了 S-AM41 和 L-AM41 支持的催化剂。NiMo/B-AM41 催化剂的优异活性可归因于高硫化度,这种高硫化度提供了足够的高度分散的Ⅱ型 MoS2 相,这些相具有最小的堆叠和适中的板坯长度。此外,双峰介孔结构促进了 4,6-DMDBT 的扩散,有利于其与活性位点的接触。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Catalysis
Journal of Catalysis 工程技术-工程:化工
CiteScore
12.30
自引率
5.50%
发文量
447
审稿时长
31 days
期刊介绍: The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes. The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods. The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.
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