Journal
SCIENTIFIC REPORTS
Volume 11, Issue 1, Pages -Publisher
NATURE PORTFOLIO
DOI: 10.1038/s41598-021-89082-x
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Funding
- Rachadapisek Sompote Endowment Fund for the Postdoctoral Fellowship, Chulalongkorn University
- National Research Council of Thailand
- International Research Network [IRN62W0001]
- CAT-REAC Industrial Project from the Thailand Science Research Council of Thailand [RDG6250033]
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The TiO2-supported Ru-based catalysts with different crystallographic compositions exhibited varying catalytic activities and selectivities in the liquid-phase hydrogenation of furfural to furfuryl alcohol. The bimetallic Ru-Co catalysts showed improved performance with increasing Co loading, attributed to the synergistic effect of the Ru-Co alloying system and the enhanced reducibility of Co oxides. The Ru-0.6Co/TiO2 catalyst demonstrated the best performance in the selective hydrogenation of furfural to furfuryl alcohol under the studied conditions.
The TiO2 supported Ru-based catalysts were prepared with 1.5 wt% Ru and 0-0.8 wt% Co on various TiO2 (anatase, rutile, P-25, and sol-gel TiO2) and studied in the liquid-phase selective hydrogenation of furfural to furfuryl alcohol (FA) under mild conditions (50 degrees C and 2 MPa H-2). The presence of high anatase crystallographic composition on TiO2 support was favorable for enhancing hydrogenation activity, while the strong interaction between Ru and TiO2 (Ru-TiOx sites) was required for promoting the selectivity to FA. The catalytic performances of bimetallic Ru-Co catalysts were improved with increasing Co loading due to the synergistic effect of Ru-Co alloying system together with the strong interaction between Ru and Co as revealed by XPS, H-2-TPR, and TEM-EDX results. The enhancement of reducibility of Co oxides in the bimetallic Ru-Co catalysts led to higher hydrogenation activity with the Ru-0.6Co/TiO2 catalyst exhibited the best performances in FA selective hydrogenation of furfural to FA under the reaction conditions used.
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