Heterogeneous Catalytic Hydrogenation of Levulinic Acid to γ-Valerolactone with Formic Acid as Internal Hydrogen Source

Abstract

As one of the most promising biomass-based platform molecules, γ-valerolactone (GVL) can be synthesized from a variety of lignocellulosic feedstocks through different hydrogen supply pathways. Among these transformation routes, the hydrogenation of levulinic acid (LA) to GVL by using formic acid (FA) as the internal hydrogen source is regarded as a critical path for the sustainable development of renewable energy systems. Although a large number of studies on the synthesis of GVL have been reported, the FA/LA catalytic system has not been interpreted as thoroughly as it should be. In this Minireview, core concerns are focused on key issues and their effects in this FA/LA catalytic system. The catalytic mechanism, together with competitive adsorption behavior between FA and LA on heterogeneous catalysts, is presented. The effects of active metal species and catalyst supports on the overall catalytic performance are summarized, and the influences of key condition parameters, including the time, temperature, FA/LA molar ratios, and aqueous solvent, are discussed. In particular, impacts and improvements of coke deposition and metal leaching, which could greatly affect the catalyst stability, are analyzed in detail. Additionally, several feasible suggestions for the enhancement of the catalytic efficiency and stability are also proposed.

Keywords: biofuels; biomass; heterogeneous catalysis; hydrogenation; sustainable chemistry.