H/D reactivity and acidity of Bronsted acid sites of MWW zeolites: Comparison with MFI zeolite
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F19%3A39914312" target="_blank" >RIV/00216275:25310/19:39914312 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/61388955:_____/19:00517215 RIV/00216208:11310/19:10403681
Výsledek na webu
<a href="https://www.sciencedirect.com/science/article/pii/S0926860X19300675?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0926860X19300675?via%3Dihub</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.apcata.2019.02.024" target="_blank" >10.1016/j.apcata.2019.02.024</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
H/D reactivity and acidity of Bronsted acid sites of MWW zeolites: Comparison with MFI zeolite
Popis výsledku v původním jazyce
Acid site strength in MWW and MFI zeolites was investigated by isotopic exchange reaction between deuterated hydroxyl groups of zeolites and ethane molecules. The course of the reaction was monitored by FT-IR spectroscopy through time changes of integral intensities of the Si(OD)Al Bronsted acid sites represented by absorption bands at 2644, 2655, and 2657 cm(-1) for MFI, MWW and MCM-36 zeolite, respectively. The rate of the reaction was described by pseudo first order kinetics and acid site strength was compared using rate constants characteristic of individual zeolites at constant temperature. The exchange reaction is significantly faster over MFI zeolite compared with MWW zeolites, suggesting a higher acid strength of Bronsted sites in MN zeolite than in MWW. In our previous study (Arean et al. Phys. Chem. Chem. Phys. 16 (2014) 10,129), we found notable discrepancy in the relation between OH group frequency shift induced by adsorption of weak base molecules like CO and N-2 and the change of adsorption enthalpy of these probe molecules for MWW zeolites, which calls into question the use of frequency shifts as a measure of acidity. Our reported results based on isotopic exchange reaction rate measurement correlate with the change of the probe molecules adsorption enthalpy involved in hydrogen bonding. Therefore, we believe that enthalpy change or H/D exchange activity measurement is more reliable method for assessment of acid strength than O-H frequency shift probed by a weak base adsorbed at a low temperature.
Název v anglickém jazyce
H/D reactivity and acidity of Bronsted acid sites of MWW zeolites: Comparison with MFI zeolite
Popis výsledku anglicky
Acid site strength in MWW and MFI zeolites was investigated by isotopic exchange reaction between deuterated hydroxyl groups of zeolites and ethane molecules. The course of the reaction was monitored by FT-IR spectroscopy through time changes of integral intensities of the Si(OD)Al Bronsted acid sites represented by absorption bands at 2644, 2655, and 2657 cm(-1) for MFI, MWW and MCM-36 zeolite, respectively. The rate of the reaction was described by pseudo first order kinetics and acid site strength was compared using rate constants characteristic of individual zeolites at constant temperature. The exchange reaction is significantly faster over MFI zeolite compared with MWW zeolites, suggesting a higher acid strength of Bronsted sites in MN zeolite than in MWW. In our previous study (Arean et al. Phys. Chem. Chem. Phys. 16 (2014) 10,129), we found notable discrepancy in the relation between OH group frequency shift induced by adsorption of weak base molecules like CO and N-2 and the change of adsorption enthalpy of these probe molecules for MWW zeolites, which calls into question the use of frequency shifts as a measure of acidity. Our reported results based on isotopic exchange reaction rate measurement correlate with the change of the probe molecules adsorption enthalpy involved in hydrogen bonding. Therefore, we believe that enthalpy change or H/D exchange activity measurement is more reliable method for assessment of acid strength than O-H frequency shift probed by a weak base adsorbed at a low temperature.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10403 - Physical chemistry
Návaznosti výsledku
Projekt
<a href="/cs/project/GBP106%2F12%2FG015" target="_blank" >GBP106/12/G015: Vývoj nových nanoporézních adsorbentů a katalyzátorů</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2019
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Applied catalysis A: General
ISSN
0926-860X
e-ISSN
—
Svazek periodika
575
Číslo periodika v rámci svazku
April
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
7
Strana od-do
180-186
Kód UT WoS článku
000462801700020
EID výsledku v databázi Scopus
2-s2.0-85062030879