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Título
Mesoporous tantalum oxide as catalyst for dehydration of glucose to 5-hydroxymethylfurfural
Autor(es)
Palabras clave
Mesoporous tantalum oxide
5-Hydroxymethylfurfural
Glucose dehydration
Levulinic acid
Clasificación UNESCO
2210.28 Química del Estado Sólido
2303 Química Inorgánica
2391 Química Ambiental
Fecha de publicación
2014
Editor
Elsevier
Citación
I. Jiménez-Morales, M. Moreno-Recio, J. Santamaría-González, P. Maireles-Torres, A. Jiménez-López, Mesoporous tantalum oxide as catalyst for dehydration of glucose to 5-hydroxymethylfurfural, Applied Catalysis B: Environmental, Volumes 154–155, 2014, Pages 190-196, ISSN 0926-3373, https://doi.org/10.1016/j.apcatb.2014.02.024. (https://www.sciencedirect.com/science/article/pii/S0926337314001179)
Resumen
[EN]Mesoporous tantalum oxide was prepared by acid hydrolysis of tantalum penta-ethoxide in the presence of a triblock co-polymer Pluronic L-121, a non-ionic surfactant, at room temperature and subsequent calcination at 550 °C for 6 h. This solid exhibits a suitable specific surface area (79 m2 g−1) and a high acidity (353 μmol NH3 g−1) with the presence of both Brönsted and Lewis acid sites, demonstrating to be active as solid acid catalyst in the dehydration of glucose to 5-hydroxymethylfurfural (HMF), in a biphasic water/methyl-iso-butyl ketone (MIBK) system. Thus, by using a glucose:catalyst weight ratio of 3:1, a glucose conversion of 69% and a HMF yield of 23% were achieved at 175 °C, and after only 90 min of reaction time. The catalytic process is selective toward HMF, which is preserved from ulterior hydration to levulinic acid. Fructose was also detected as by-product of glucose isomerisation with 14% of selectivity. The catalyst is very stable, since no leaching of tantalum species to the liquid phase was found; moreover, the catalytic performance of this acid solid is well recovered after calcination at 550 °C for 2 h.
URI
ISSN
0926-3373
DOI
10.1016/j.apcatb.2014.02.024
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