Highly Active Bulk Mo(W)S2 Hydrotreating Catalysts Synthesized by Etching out of the Carrier from Supported Mono- and Bimetallic Sulfides
- Authors: Kokliukhin A.S.1,2, Mozhaev A.V.1, Nikulshina M.S.1,2, Lancelot C.2, Blanchard P.2, Lamonier C.2, Nikulshin P.A.1,3
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Affiliations:
- Samara State Technical University
- Université Lille1, UCCS
- All-Russia Research Institute for Oil Refining
- Issue: Vol 59, No Suppl 1 (2019)
- Pages: S53-S59
- Section: Article
- URL: https://ogarev-online.ru/0965-5441/article/view/181038
- DOI: https://doi.org/10.1134/S0965544119130085
- ID: 181038
Cite item
Abstract
A bulk MoWS2 catalyst has been synthesized by acid etching of the carrier from the supported MoWS2/Al2O3 catalyst obtained on the basis of the mixed bimetallic heteropoly acid (HPA) H4[SiMo3W9O40]. As reference samples, monometallic MoS2 and WS2 catalysts have been prepared from the corresponding supported analogues, as well as a Mo + WS2 sample based on a mechanical mixture of monometallic HPA in the atomic ratio of Mo/W = 1/3. The catalytic properties of the synthesized catalysts have been studied in model reactions of hydrodesulfurization (HDS) of dibenzthiophene (DBT) and hydrogenation (HYD) of naphthalene in a flow unit. It has been shown that the catalytic activity of the samples in both the DBT HDS and naphthalene HYD reactions increases in the following order: MoS2 < WS2 < Mo + WS2\( \ll \) MoWS2. It has been found that the bulk tungsten-containing catalysts exhibit higher specific catalytic activity than the supported counterparts. Increased values of hydrogen uptake according to the results of hydrogen temperature-programmed reduction for the bulk catalysts indicate an increase in the number of active sites and the formation of a more effective active phase compared to supported catalysts.
Keywords
About the authors
A. S. Kokliukhin
Samara State Technical University; Université Lille1, UCCS
Email: aleks.mozhaev@gmail.com
Russian Federation, Samara, 443100; Cité Scientifique, Villeneuved’Ascq, Bat. C3, Lille, 59655
A. V. Mozhaev
Samara State Technical University
Author for correspondence.
Email: aleks.mozhaev@gmail.com
Russian Federation, Samara, 443100
M. S. Nikulshina
Samara State Technical University; Université Lille1, UCCS
Email: aleks.mozhaev@gmail.com
Russian Federation, Samara, 443100; Cité Scientifique, Villeneuved’Ascq, Bat. C3, Lille, 59655
C. Lancelot
Université Lille1, UCCS
Email: aleks.mozhaev@gmail.com
France, Cité Scientifique, Villeneuved’Ascq, Bat. C3, Lille, 59655
P. Blanchard
Université Lille1, UCCS
Email: aleks.mozhaev@gmail.com
France, Cité Scientifique, Villeneuved’Ascq, Bat. C3, Lille, 59655
C. Lamonier
Université Lille1, UCCS
Email: aleks.mozhaev@gmail.com
France, Cité Scientifique, Villeneuved’Ascq, Bat. C3, Lille, 59655
P. A. Nikulshin
Samara State Technical University; All-Russia Research Institute for Oil Refining
Email: aleks.mozhaev@gmail.com
Russian Federation, Samara, 443100; Moscow, 111116
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