Mesoporous Ti–W oxide: synthesis, characterization, and performance in selective hydrogenolysis of glycerol

Mesoporous Ti-W oxides, bearing high surface area, large pore volume, uniform pore size and tunable W/Ti ratios in a wide range (10-40 mol%), were successfully fabricated viaan evaporation-induced self-assembly (EISA) strategy. In this approach, the incorporation of W species not only effectively re...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2013-01, Vol.1 (11), p.3724-3732
Hauptverfasser: Zhang, Yanhua, Zhao, Xiao-Chen, Wang, Yao, Zhou, Likun, Zhang, Junying, Wang, Jia, Wang, Aiqin, Zhang, Tao
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Mesoporous Ti-W oxides, bearing high surface area, large pore volume, uniform pore size and tunable W/Ti ratios in a wide range (10-40 mol%), were successfully fabricated viaan evaporation-induced self-assembly (EISA) strategy. In this approach, the incorporation of W species not only effectively resulted in well-ordered mesoporous structures when calcined below 400 degree C but also modified the acidic properties of the obtained oxide composites. The optimal acid amounts (0.47-0.67 mmol g super(-1) for 400 degree C calcinations, 0.25-0.27 mmol g super(-1) for 500 degree C calcinations) were obtained when the W concentration was between 10 and 20 mol%. When calcined at 500 degree C, Broensted acids were generated in Ti sub(90)W sub(10)-500 and Ti sub(80)W sub(20)-500. The catalytic performance of these mesoporous solid acids in glycerol hydrogenolysis was studied with a loading of 2 wt% Pt. Pt/Ti sub(100-n)W sub(n)-500s exhibited high selectivity to 1,3-propanediol (33.5% and 40.3%) and promising catalytic activities (18.4% and 24.2% glycerol conversion) when nis 10 and 20, respectively. This work presents a step forward in the development of highly efficient glycerol hydrogenolysis catalysts and a new understanding of the reaction mechanism of glycerol hydrogenolysis to 1,3-propanediol.
ISSN:2050-7488
2050-7496
DOI:10.1039/c3ta10217c