One-pot reductive liquefaction of sawdust to renewables over MoOx–Al2O3 variants: insight into structure–activity relationships

Abstract

Valorization of forest residual products can offer a vital pathway to derive bio-based chemicals and fuel components. Herein, we report the effective and direct conversion of sawdust biomass over a supported Mo-oxide catalyst that results in a dominant fraction of aliphatic/cyclic alkanes and alkylbenzenes with low residual solids. The reductive liquefaction was conducted in an autoclave reactor using a series of MoO_x–Al₂O₃ variants in the range of 340–400 °C with an initial H₂ pressure of 35 bar for 4 h. At 340 °C, a correlation between Mo-loadings and reactivity for depolymerization and hydrodeoxygenation was found optimal for a surface density of 3.2 Mo-atoms per nm² corresponding to 8 wt% Mo-loading. The liquefied fraction showed high selectivity (∼38%) for the formation of cycloalkanes and alkylbenzenes. At higher temperatures (400 °C) enhanced reactivity over the optimal catalyst showed higher cycloalkane and alkylbenzenes formation (∼57%) at a low biomass-to-catalyst feed mass ratio (3 : 1). At a higher ratio (10 : 1), alkylphenols (∼41%) are the leading product fraction followed by cycloalkanes and alkylbenzenes (∼34%) with a high liquefied monomer bio-oil product yield of 39.4 wt%. Catalyst characterization via XRD, Raman, H₂-TPR, and XPS analysis revealed that the origin for this reactivity arises from the Mo species formed and stabilized over the support surface. A well dispersed, octahedral, higher fraction of easily reducible Mo-species (Mo⁵⁺) was evident over the optimal catalyst which enables enhanced C–O cleavage facilitating the hydrodeoxygenation reaction. Moreover, the solid residue yield could be reduced to below 5 wt% by optimizing the reaction conditions and particle size of the sawdust.