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

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F21%3A00120772" target="_blank" >RIV/00216224:14310/21:00120772 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1016/j.micromeso.2020.110682" target="_blank" >http://dx.doi.org/10.1016/j.micromeso.2020.110682</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.micromeso.2020.110682" target="_blank" >10.1016/j.micromeso.2020.110682</a>

Jazyk výsledku

angličtina

Název v původním jazyce

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

Popis výsledku v původním jazyce

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.

Název v anglickém jazyce

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

Popis výsledku anglicky

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.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10402 - Inorganic and nuclear chemistry

Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2021

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Microporous and Mesoporous Materials

ISSN

1387-1811

e-ISSN

1873-3093

Svazek periodika

311

Číslo periodika v rámci svazku

February 2021

Stát vydavatele periodika

NL - Nizozemsko

Počet stran výsledku

9

Strana od-do

1-9

Kód UT WoS článku

000600420800008

EID výsledku v databázi Scopus

2-s2.0-85093096235