Potassium-modified bifunctional MgAl-SBA-15 for aldol condensation of furfural and acetone
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F23%3A43926666" target="_blank" >RIV/60461373:22310/23:43926666 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/60461373:22320/23:43926666 RIV/60461373:22350/23:43926666
Výsledek na webu
<a href="https://pubs.rsc.org/en/content/articlehtml/2023/se/d3se00444a?page=search" target="_blank" >https://pubs.rsc.org/en/content/articlehtml/2023/se/d3se00444a?page=search</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/d3se00444a" target="_blank" >10.1039/d3se00444a</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Potassium-modified bifunctional MgAl-SBA-15 for aldol condensation of furfural and acetone
Popis výsledku v původním jazyce
The aldol condensation of furfural and acetone followed by hydrodeoxygenation into bio-jet fuel range alkanes and bio-polyester diols has attracted intensive interest in recent years. Such sequential reactions require a careful tailoring of one or more catalysts consisting of metal and acid–base active sites that can efficiently promote the two step cascade aldol condensation and hydrodeoxygenation. Here, we have begun developing a prominent base catalyst for mild aldol condensation of furfural and acetone by synthesizing acid–base bifunctional MgAl-SBA-15 and further modifying it with potassium. The catalyst with the highest basic site loading of 0.27 mmol g−1 showed a furfural conversion of 83% and 99% total selectivity to products comprising 54% 4-(2-furyl)-4-hydroxy-butan-2-one (FAc-OH, a C8 alcohol intermediate) and 23% of each 4-(2-furyl)-3-buten-2-one (FAc) and 1,4-pentadiene-3-one,1,5-di-2-furanyl (F2Ac) (C8 and C13 aldol condensation products, respectively) after 3 hours of reaction, at 50 °C. Though a higher loading of potassium causes severe blockages of mesopores and inaccessible acid sites, the catalyst could still be regenerated by open-air calcination and be re-used for considerable cycles with fair catalytic performances. Overall, the present study can be the stepping stone for future investigations on further tuning of non-interfering active sites in SBA-15 to promote an efficient one-pot transformation of furfural and acetone via the two-step cascade aldol condensation and hydrodeoxygenation.
Název v anglickém jazyce
Potassium-modified bifunctional MgAl-SBA-15 for aldol condensation of furfural and acetone
Popis výsledku anglicky
The aldol condensation of furfural and acetone followed by hydrodeoxygenation into bio-jet fuel range alkanes and bio-polyester diols has attracted intensive interest in recent years. Such sequential reactions require a careful tailoring of one or more catalysts consisting of metal and acid–base active sites that can efficiently promote the two step cascade aldol condensation and hydrodeoxygenation. Here, we have begun developing a prominent base catalyst for mild aldol condensation of furfural and acetone by synthesizing acid–base bifunctional MgAl-SBA-15 and further modifying it with potassium. The catalyst with the highest basic site loading of 0.27 mmol g−1 showed a furfural conversion of 83% and 99% total selectivity to products comprising 54% 4-(2-furyl)-4-hydroxy-butan-2-one (FAc-OH, a C8 alcohol intermediate) and 23% of each 4-(2-furyl)-3-buten-2-one (FAc) and 1,4-pentadiene-3-one,1,5-di-2-furanyl (F2Ac) (C8 and C13 aldol condensation products, respectively) after 3 hours of reaction, at 50 °C. Though a higher loading of potassium causes severe blockages of mesopores and inaccessible acid sites, the catalyst could still be regenerated by open-air calcination and be re-used for considerable cycles with fair catalytic performances. Overall, the present study can be the stepping stone for future investigations on further tuning of non-interfering active sites in SBA-15 to promote an efficient one-pot transformation of furfural and acetone via the two-step cascade aldol condensation and hydrodeoxygenation.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
20704 - Energy and fuels
Návaznosti výsledku
Projekt
—
Návaznosti
O - Projekt operacniho programu
Ostatní
Rok uplatnění
2023
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Sustainable Energy and Fuels
ISSN
2398-4902
e-ISSN
—
Svazek periodika
7
Číslo periodika v rámci svazku
13
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
13
Strana od-do
3047-3059
Kód UT WoS článku
000998994900001
EID výsledku v databázi Scopus
2-s2.0-85164963925