Počet záznamů: 1  

Reactivity of internal vs. external Brønsted acid sites in nanosponge MFI: H/D exchange kinetic study

  1. 1.
    SYSNO ASEP0553192
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevReactivity of internal vs. external Brønsted acid sites in nanosponge MFI: H/D exchange kinetic study
    Tvůrce(i) 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, ORCID
    Číslo článku111717
    Zdroj.dok.Microporous and Mesoporous Materials. - : Elsevier - ISSN 1387-1811
    Roč. 332, February (2022)
    Poč.str.8 s.
    Jazyk dok.eng - angličtina
    Země vyd.NL - Nizozemsko
    Klíč. slovaacidity ; zeolites ; MFI ; isotopic exchange ; two-dimensional ; nanosponge ; DFT ; theory ; external sites
    Obor OECDPhysical chemistry
    CEPGA19-19542S GA ČR - Grantová agentura ČR
    Výzkumná infrastrukturae-INFRA CZ - 90140 - CESNET, zájmové sdružení právnických osob
    Způsob publikováníOmezený přístup
    Institucionální podporaUOCHB-X - RVO:61388963
    UT WOS000761764300004
    EID SCOPUS85123740602
    DOI10.1016/j.micromeso.2022.111717
    AnotaceThe 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).
    PracovištěÚstav organické chemie a biochemie
    Kontaktasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Jana Procházková, Tel.: 220 183 418
    Rok sběru2023
    Elektronická adresahttps://doi.org/10.1016/j.micromeso.2022.111717
Počet záznamů: 1  

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