Catalytic Activity of CoMo Sulfide Catalysts Supported on Natural and Synthetic Aluminosilicates in Hydrodesulfurization of 4,6-Dimethyldibenzothiophene

CoMo sulfide catalysts supported on an MCM-41-type ordered mesoporous silica and on a hierarchical aluminosilicate material based on halloysite nanotubes (MCM-41@HNT) were synthesized by incipient wetness impregnation. Both the supports and related catalysts were characterized by low-temperature nitrogen adsorption–desorption, energy dispersive X-ray fluorescence analysis, FTIR spectroscopy of adsorbed pyridine, transmission electron microscopy, and X-ray photoelectron spectroscopy. The catalyst samples were further tested in hydrodesulfurization of 4,6-dimethyldibenzothiophene. The MCM-41@HNT-supported catalyst exhibited the greatest activity in the main reaction (hydrodesulfurization) due to its hierarchical porous structure and the presence of high-temperature Brønsted acid sites.

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Journal
Petroleum Chemistry
Published
2025-04-01
DOI
https://doi.org/10.1134/s0965544125600778
Primary Topic
Catalysis and Hydrodesulfurization Studies
Type
article
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article

Catalytic Activity of CoMo Sulfide Catalysts Supported on Natural and Synthetic Aluminosilicates in Hydrodesulfurization of 4,6-Dimethyldibenzothiophene

N. A. Vinogradov, А. P. Glotov, А. В. Вутолкина, E. M. Smirnova et al.
Petroleum Chemistry
Catalysis and Hydrodesulfurization Studies
article

Catalytic Activity of CoMo Sulfide Catalysts Supported on Natural and Synthetic Aluminosilicates in Hydrodesulfurization of 4,6-Dimethyldibenzothiophene

N. A. Vinogradov, А. P. Glotov, А. В. Вутолкина, E. M. Smirnova, G. O. Zasypalov, А. А. Pimerzin, V. I. Elizarova, E. S. Abramov, V. A. Klimovskii
article en

Abstract

CoMo sulfide catalysts supported on an MCM-41-type ordered mesoporous silica and on a hierarchical aluminosilicate material based on halloysite nanotubes (MCM-41@HNT) were synthesized by incipient wetness impregnation. Both the supports and related catalysts were characterized by low-temperature nitrogen adsorption–desorption, energy dispersive X-ray fluorescence analysis, FTIR spectroscopy of adsorbed pyridine, transmission electron microscopy, and X-ray photoelectron spectroscopy. The catalyst samples were further tested in hydrodesulfurization of 4,6-dimethyldibenzothiophene. The MCM-41@HNT-supported catalyst exhibited the greatest activity in the main reaction (hydrodesulfurization) due to its hierarchical porous structure and the presence of high-temperature Brønsted acid sites.

Petroleum ChemistryVol. 65(4)
Gazprom (Russia) (RU), Gubkin Russian State University of Oil and Gas (RU), Samara State Technical University (RU)
Openalex Percentile: Top 85%
Catalysis and Hydrodesulfurization Studies
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