2023
Hydrophobicity Boosts Catalytic Activity: The Tailoring of Aluminosilicates with Trimethylsilyl Groups
LEONOVÁ, Lucie, Zdeněk MORAVEC, Petr SAZAMA, Jana PASTVOVA, Libor KOBERA et. al.Základní údaje
Originální název
Hydrophobicity Boosts Catalytic Activity: The Tailoring of Aluminosilicates with Trimethylsilyl Groups
Autoři
LEONOVÁ, Lucie (203 Česká republika, domácí), Zdeněk MORAVEC (203 Česká republika, domácí), Petr SAZAMA, Jana PASTVOVA, Libor KOBERA, Jiri BRUS a Aleš STÝSKALÍK (203 Česká republika, garant, domácí)
Vydání
ChemCatChem, Wiley-VCH GmbH, 2023, 1867-3880
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10402 Inorganic and nuclear chemistry
Stát vydavatele
Německo
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.500 v roce 2022
Kód RIV
RIV/00216224:14310/23:00131009
Organizační jednotka
Přírodovědecká fakulta
UT WoS
001005890400001
Klíčová slova anglicky
acid catalysis; aluminosilicate; epoxide ring opening; ethanol dehydration; hydrophobicity
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 15. 10. 2024 14:57, Ing. Jana Kuchtová
Anotace
V originále
Introducing organic groups into metal silicate catalysts and thus supposedly changing the surface hydrophobicity has been shown to enhance the catalyst performance in various reactions. However, the organic groups introduction does not unambiguously guarantee hydrophobicity control. Therefore, a thorough characterization is necessary to provide a complete view of the interaction between the catalyst surface, reactants, and products. Herein, an aluminosilicate catalyst with well-dispersed Al atoms was prepared via the non-hydrolytic sol-gel method. This material was post-synthetically modified with trimethylsilyl groups; their number on the catalyst surface was controlled via a temperature-vacuum pretreatment. In such a way, aluminosilicate materials with similar porosity, structure, and acid site strength and quality were obtained. Notably, the water sorption measurements showed that trimethylsilylated aluminosilicates adsorb 2.5–3 times less water than the parent material (p/p0=0.3). The turn-over-frequency in epoxide ring opening and ethanol dehydration scaled up with the number of trimethylsilyl groups grafted on the catalyst surface. Particularly, the heavily trimethylsilylated sample achieved three to five times higher turnover-frequency in styrene oxide aminolysis than the parent aluminosilicate material. To the best of the authors’ knowledge, it exhibited the most active Al sites for epoxide aminolysis in the present literature.
Návaznosti
GJ20-03636Y, projekt VaV |
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MUNI/A/1209/2022, interní kód MU |
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MUNI/J/0007/2021, interní kód MU |
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90127, velká výzkumná infrastruktura |
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