4.7 Article

Design of active phase structure with high activity and stability in residue hydrotreating reactions

期刊

FUEL
卷 360, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2023.130288

关键词

Residue; Hydrodesulfurization; Active phase; Evolution pattern; Stability

向作者/读者索取更多资源

By strengthening metal-support interaction (MSI) and metal dispersion, a catalyst with high activity and long-term stability was designed. The impacts of pseudo-boehmite and catalyst calcination temperature on surface properties were thoroughly investigated.
The catalyst with well-dispersed (Ni)MoS2 active phase characteristic of short slab length and low stacking numbers was designed by strengthening metal-support interaction (MSI) and metal dispersion, which displayed high activity and long-term stability in real-life residue hydrodesulfurization (HDS) reactions. Furthermore, the impacts of pseudo-boehmite and catalyst calcination temperature on surface properties were thoroughly investigated. Mo equilibrium adsorption method, Al27 NMR, XRD, Raman, UV-Vis DRS, and H2-TPR characterization showed that the hydroxyl groups concentration and tetrahedral cation vacancies increased upon reducing the pseudo-boehmite extrudates calcination temperature. Increasing calcination temperature of the catalysts further strengthened MSI, resulted in well-dispersed Mo species with enhanced MSI. Therefore, well-dispersed (Ni)MoS2 active phase was acquired on novel designed catalyst. XPS coupled with HRTEM indicated that the more potential active sites, less propensity for active phase evolution and gradual increase in sulfidation degree with processing time contributed to the high HDS performance of the designed active phase. This work can deepen our understanding toward evolution pattern of active phase during residue HDS catalysts, and give guidance for developing high performance catalyst by strengthening MSI and enhancing metal dispersion.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据