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Reactivity of internal vs. external Brønsted acid sites in nanosponge MFI: H/D exchange kinetic study
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SYSNO ASEP 0553192 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Reactivity of internal vs. external Brønsted acid sites in nanosponge MFI: H/D exchange kinetic study Author(s) Bulánek, R. (CZ)
Vaculík, J. (CZ)
Veselý, O. (CZ)
Přech, J. (CZ)
Kubů, M. (CZ)
Rubeš, Miroslav (UOCHB-X) RID, ORCID
Bludský, Ota (UOCHB-X) RID, ORCIDArticle number 111717 Source Title Microporous and Mesoporous Materials. - : Elsevier - ISSN 1387-1811
Roč. 332, February (2022)Number of pages 8 s. Language eng - English Country NL - Netherlands Keywords acidity ; zeolites ; MFI ; isotopic exchange ; two-dimensional ; nanosponge ; DFT ; theory ; external sites OECD category Physical chemistry R&D Projects GA19-19542S GA ČR - Czech Science Foundation (CSF) Research Infrastructure e-INFRA CZ - 90140 - CESNET, zájmové sdružení právnických osob Method of publishing Limited access Institutional support UOCHB-X - RVO:61388963 UT WOS 000761764300004 EID SCOPUS 85123740602 DOI 10.1016/j.micromeso.2022.111717 Annotation The strength of Brønsted acid sites (BAS) affects the properties of 2D and hierarchical zeolites, but the relative contribution of internal and external BAS remains unknown. Accordingly, this study aims to assess the acidity of external and internal BAS in nanosponge-like MFI zeolites by comparatively analyzing hydrogen–deuterium exchange kinetics between zeolitic deuteroxyl groups and C2H6 molecules monitored by in-situ FTIR spectroscopy. For this purpose, (i) a sample pre-treatment procedure was specifically developed to deuterate only internal or only external acid sites using 2,6-di-tert-butylpyridine (DTBP) as a masking agent and (ii) DFT modeling of surface BAS was performed. Theoretical models of the thin MFI layer revealed that the external surface of MFI crystals contains three types of BAS: (i) BAS positioned in 5-membered rings, either shielded by silanol nests, rendering the site inaccessible for DTBP or yielding a very low adsorption energy for ethane, (ii) BAS pointing into the pores, due to the presence of aluminol, which hinders DTBP accessibility, or the BAS undergoes transformation to a three-coordinate aluminium site, and (iii) BAS accessible to both DTBP and ethane. The results from our kinetics measurements showed that H/D exchange at external BAS of nanosponge MFI zeolites is faster than at internal BAS (rate constants at 425 °C: 3.8 10−3 vs. 2.4 10−3 s−1 for external and internal BAS, respectively), but this cannot be attributed to the effect of diffusion. Therefore, the differences in exchange kinetics between external and internal BAS are given by mutual interplay of subtle differences in the corresponding activation barriers (113 vs. 117 kJ/mol for external and internal BAS, respectively) and pre-exponential terms (1.09 106 vs. 1.45 106 s−1 for external and internal BAS, respectively). Workplace Institute of Organic Chemistry and Biochemistry Contact asep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Jana Procházková, Tel.: 220 183 418 Year of Publishing 2023 Electronic address https://doi.org/10.1016/j.micromeso.2022.111717
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