Elucidation of the Catalytic Pathway for the Direct Conversion of Furfuryl Alcohol into γ-Valerolactone over Al2O3-SiO2 Catalysts.

The one-pot conversion of furfuryl alcohol (FA) into GVL was investigated over the sol-gel-synthesized Al2O3-SiO2 (AlSi) catalysts with various Al2O3 loadings (0.2-10 wt %) and commercial zeolites including MFI-1, H-ZSM5, H-beta, and HY-15 in a batch reactor under mild reaction conditions (130 °C, 1 bar N2, and 15-120 min). The reaction pathways depend largely on the acid properties of the catalysts, especially the types of Bronsted (B) and Lewis (L) acid sites. A tandem alcoholysis/hydrogenation/cyclization sequence is dominant on the AlSi catalysts (Al ≥ 4%) and all the zeolites except MFI-1, resulting in complete conversion of FA and GVL with an yield 64-75% with IPL as the major side-product, regardless of the differences in their B/L ratios 0.06-1.35. In the absence of B acid sites (i.e., 0.2% AlSi and MFI-1 catalysts), FA could be straightforwardly converted into GVL on the weak Lewis acid sites from the isolated silanol groups using 2-propanol as a hydrogen source. The AlSi catalysts are promising tunable catalysts for FA conversion with good recyclability.

Effects of TiO2 structure and Co addition as a second metal on Ru-based catalysts supported on TiO2 for selective hydrogenation of furfural to FA.

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 °C and 2 MPa H2). 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, H2-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.