Aldol condensation of furfural with acetone over ion-exchanged and impregnated potassium BEA zeolites
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22350%2F16%3A43901751" target="_blank" >RIV/60461373:22350/16:43901751 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/61388955:_____/16:00472522 RIV/62243136:_____/16:N0000005 RIV/00216275:25310/16:39902167
Výsledek na webu
<a href="http://www.sciencedirect.com.ezproxy.vscht.cz/science/article/pii/S1381116916303867" target="_blank" >http://www.sciencedirect.com.ezproxy.vscht.cz/science/article/pii/S1381116916303867</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.molcata.2016.09.014" target="_blank" >10.1016/j.molcata.2016.09.014</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Aldol condensation of furfural with acetone over ion-exchanged and impregnated potassium BEA zeolites
Popis výsledku v původním jazyce
Potassium-containing BEA zeolites were prepared by ion-exchange from NH4-BEA with potassium nitrateaqueous solution or ion-exchange combined with impregnation. The samples were used as basic catalystsfor aldol condensation of furfural and acetone studied in a batch reactor at 100°C, autogenous pressureand a reaction time of 2 h. To establish a relationship between physico-chemical properties and catalyticbehavior of BEA zeolites, the samples were characterized by XRD, N2adsorption, FTIR, calorimetry, andTGA. The ion-exchanged K-BEA catalysts exhibited low activity in the aldol condensation because of aweak strength of intrinsic basic sites. In contrast, the samples prepared by ion exchange combined withimpregnation possessed strong basic sites, plausibly K2O clusters, and demonstrated appreciable activityin the aldol condensation. TGA results proved that, in contrast to acidic zeolites, basic sites of impregnatedBEA samples hardly contribute to the formation of heavy carbonaceous deposits during the reaction whatcould be advantageous for the stable behavior of catalysts.
Název v anglickém jazyce
Aldol condensation of furfural with acetone over ion-exchanged and impregnated potassium BEA zeolites
Popis výsledku anglicky
Potassium-containing BEA zeolites were prepared by ion-exchange from NH4-BEA with potassium nitrateaqueous solution or ion-exchange combined with impregnation. The samples were used as basic catalystsfor aldol condensation of furfural and acetone studied in a batch reactor at 100°C, autogenous pressureand a reaction time of 2 h. To establish a relationship between physico-chemical properties and catalyticbehavior of BEA zeolites, the samples were characterized by XRD, N2adsorption, FTIR, calorimetry, andTGA. The ion-exchanged K-BEA catalysts exhibited low activity in the aldol condensation because of aweak strength of intrinsic basic sites. In contrast, the samples prepared by ion exchange combined withimpregnation possessed strong basic sites, plausibly K2O clusters, and demonstrated appreciable activityin the aldol condensation. TGA results proved that, in contrast to acidic zeolites, basic sites of impregnatedBEA samples hardly contribute to the formation of heavy carbonaceous deposits during the reaction whatcould be advantageous for the stable behavior of catalysts.
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
CA - Anorganická chemie
OECD FORD obor
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Návaznosti výsledku
Projekt
<a href="/cs/project/GBP106%2F12%2FG015" target="_blank" >GBP106/12/G015: Vývoj nových nanoporézních adsorbentů a katalyzátorů</a><br>
Návaznosti
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Ostatní
Rok uplatnění
2016
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal Of Molecular Catalysis A-Chemical
ISSN
1381-1169
e-ISSN
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Svazek periodika
424
Číslo periodika v rámci svazku
1 December 2016
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
11
Strana od-do
358-368
Kód UT WoS článku
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EID výsledku v databázi Scopus
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