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The deactivation of acidic sites of NiMo/B2O3–Al2O3 catalysts during vegetable oil hydrodeoxygenation studied by EPR spectroscopy Full article

Journal Magnetic Resonance in Chemistry
ISSN: 0749-1581 , E-ISSN: 1097-458X
Output data Year: 2021, Volume: 59, Pages: 600-607 Pages count : 8 DOI: 10.1002/mrc.5126
Tags EPR; acidic sites; carbon deposits; NiMo catalysts; modified alumina
Authors Yurpalov Vyacheslav L. 1 , Neponiashchii Aleksandr A. 1 , Drozdov Vladimir A. 1 , Antonicheva Nina V. 1 , Buluchevskiy Evgeniy A. 1 , Lavrenov Aleksandr V. 1
Affiliations
1 Center of New Chemical Technologies BIC, Boreskov Institute of Catalysis

Funding (1)

1 Ministry of Science and Higher Education of the Russian Federation V. 47

Abstract: This paper presents the study results of NiMo/B2O3-Al2O3 (0-30 % wt. of B2O3) catalysts for vegetable oil hydrodeoxygenation before and after catalytic tests by different EPR methodologies. For the initial catalysts, the concentration of Brønsted acidic sites (BAS) determined by probe EPR with perylene increases linearly with an increase in the modifier (B2O3) content in the samples. It was found that the isomerization activity of the catalysts is increases with increasing the concentration of determined BAS. As for the spent catalysts, linear correlation of paramagnetic species concentration with the content of carbon deposits (determined by TGA/DTA) was found. The main reasons for the NiMo/B2O3-Al2O3 catalysts deactivation over the formation of carbon deposits related to the participation of acidic sites (both Lewis and Brønsted) in the polycondensation of hydrocarbons via radical species are also proposed.
Cite: Yurpalov V.L. , Neponiashchii A.A. , Drozdov V.A. , Antonicheva N.V. , Buluchevskiy E.A. , Lavrenov A.V.
The deactivation of acidic sites of NiMo/B2O3–Al2O3 catalysts during vegetable oil hydrodeoxygenation studied by EPR spectroscopy
Magnetic Resonance in Chemistry. 2021. V.59. P.600-607. DOI: 10.1002/mrc.5126 WOS Scopus РИНЦ OpenAlex
Dates:
Submitted: Oct 14, 2020
Accepted: Dec 23, 2020
Published online: Jan 4, 2021
Published print: Apr 27, 2021
Identifiers:
Web of science: WOS:000604531000001
Scopus: 2-s2.0-85099034311
Elibrary: 45023209
OpenAlex: W3117330271
Citing:
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Web of science 2
Scopus 3
OpenAlex 2
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