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Effect of support composition on acid properties and deactivation of Pt/WO3–Al2O3 catalysts for vegetable oil hydrodeoxygenation by different approaches of EPR spectroscopy Full article

Journal Research on Chemical Intermediates
ISSN: 0922-6168 , E-ISSN: 1568-5675
Output data Year: 2026, DOI: 10.1007/s11164-026-06070-4
Tags Hydrodeoxygenation of vegetable oil, surface acid sites, supported bifunctional Pt catalysts, electron paramagnetic resonance, thermal analysis
Authors Yurpalov Vyacheslav L. 1 , Nepomnyashchii Aleksandr A. 1 , Lavrenov Aleksandr V. 1
Affiliations
1 Center of New Chemical Technologies BIC, Boreskov Institute of Catalysis, 54 Neftezavodskaya St., Omsk, Russia, 644040

Funding (1)

1 Ministry of Science and Higher Education of the Russian Federation FWUR-2024-0039

Abstract: The effect of WO3 modifier content (0–25 wt%) for a series of bifunctional Pt/WO3–Al2O3 catalysts (0.5 wt% Pt) for the hydrodeoxygenation of vegetable oil on the concentration of acid sites and the tendency to deactivation was studied using classical and probe EPR methodologies, as well as thermal analysis. It was found that high Brønsted acid sites (BAS) concentration, determined by probe EPR with perylene molecules, promotes more intense side processes of carbon deposit formation with paramagnetic sites in the structure. A probable mechanism for the formation of EPR-detectable carbon sites through cracking, cyclization, condensation, and aromatization reactions involving carbocations is proposed. The possibility of oxidative regeneration of active BAS in catalysts with EPR monitoring is demonstrated.
Cite: Yurpalov V.L. , Nepomnyashchii A.A. , Lavrenov A.V.
Effect of support composition on acid properties and deactivation of Pt/WO3–Al2O3 catalysts for vegetable oil hydrodeoxygenation by different approaches of EPR spectroscopy
Research on Chemical Intermediates. 2026. DOI: 10.1007/s11164-026-06070-4 WOS Scopus
Dates:
Submitted: Jun 3, 2026
Accepted: Jul 19, 2026
Published online: Jul 25, 2026
Identifiers:
≡ Web of science: WOS:001829774600001
≡ Scopus: 2-s2.0-105045644287
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