Synthesis of high surface area aluminophosphate and -phosphonate xerogels by non-hydrolytic sol-gel reactions

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Publikace nespadá pod Filozofickou fakultu, ale pod Přírodovědeckou fakultu. Oficiální stránka publikace je na webu muni.cz.
Název česky Syntéza alumofosfátových a fosfonátových xerogelů s vysokým měrným povrchem pomocí nehydrolytických sol-gelových metod.
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MACHÁČ Petr ALAUZUN Johan G STÝSKALÍK Aleš DEBECKER Damien P MUTIN Hubert P PINKAS Jiří

Rok publikování 2021
Druh Článek v odborném periodiku
Časopis / Zdroj Microporous and Mesoporous Materials
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www http://dx.doi.org/10.1016/j.micromeso.2020.110682
Doi http://dx.doi.org/10.1016/j.micromeso.2020.110682
Klíčová slova Aluminophosphates; Aluminophosphonates; Non-hydrolytic; Sol-gel; Silylamine elimination; Mesoporous; Hybrid; Xerogel; Surface area; Catalysis
Popis We disclose the preparation of high-surface-area mesoporous aluminophosphates and aluminophosphonates by the non-hydrolytic sol-gel reactions (NHSG) of Al(NMe2)3 with trimethylsilylated phosphate, phosphonates, and bis-phosphonates) in dry toluene. The reactions proceed by silylamine elimination of Me3SiNMe2 to provide organic-inorganic hybrid xerogels with properties influenced by organic substituents and the Al:P ratio of the precursors.Dried xerogels exhibit large surface areas (up to 1000 m2 g-1) and matrices based on condensed Al-O-P networks. They stay stable under relatively harsh thermal conditions. 27Al, 13C, and 29Si solid-state NMR spectroscopy was employed to characterize the aluminum coordination and the residual amido and trimethylsilyl groups. The catalytic performance of NHSG prepared material was examined in gas-phase dehydration of ethanol to ethylene exhibiting conversion and selectivity comparable to weak solid acid benchmark catalysts. The number of unreacted surface groups was determined by gravimetric measurements and by thermal analysis (TG-DSC). These residual groups have the potential to be used in post-synthetic grafting of catalytically active metal centers.
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