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High performing and stable supported nano-alloys for the catalytic hydrogenation of levulinic acid to γ-valerolactone

Authors :
Luo, Wenhao
Meenakshisundaram, Sankar
Beale, Andrew M.
He, Qian
Kiely, Christopher J.
Bruijnincx, Pieter C. A.
Weckhuysen, Bert M.
Inorganic Chemistry and Catalysis
Sub Inorganic Chemistry and Catalysis
Source :
Nature Communications, Nature Communications [E], 6. Nature Publishing Group, 'Nature Communications ', vol: 6, pages: 6540-1-6540-10 (2015)
Publication Year :
2015
Publisher :
Springer Science and Business Media LLC, 2015.

Abstract

The catalytic hydrogenation of levulinic acid, a key platform molecule in many biorefinery schemes, into γ-valerolactone is considered as one of the pivotal reactions to convert lignocellulose-based biomass into renewable fuels and chemicals. Here we report on the development of highly active, selective and stable supported metal catalysts for this reaction and on the beneficial effects of metal nano-alloying. Bimetallic random alloys of gold-palladium and ruthenium-palladium supported on titanium dioxide are prepared with a modified metal impregnation method. Gold-palladium/titanium dioxide shows a marked,~27-fold increase in activity (that is, turnover frequency of 0.1 s−1) compared with its monometallic counterparts. Although ruthenium-palladium/titanium dioxide is not only exceptionally active (that is, turnover frequency of 0.6 s−1), it shows excellent, sustained selectivity to γ-valerolactone (99%). The dilution and isolation of ruthenium by palladium is thought to be responsible for this superior catalytic performance. Alloying, furthermore, greatly improves the stability of both supported nano-alloy catalysts.<br />The hydrogenation of leuvinic acid to γ-valerolactone is an important step in the conversion of lignocellulose to high value chemicals. Here, the authors report that bimetallic alloys are active and stable catalysts for this reaction, and attribute this to geometric and electronic effects.

Details

ISSN :
20411723
Volume :
6
Database :
OpenAIRE
Journal :
Nature Communications
Accession number :
edsair.doi.dedup.....b92319e3859202df07744dfbc0bbfae2
Full Text :
https://doi.org/10.1038/ncomms7540