Enhanced performance and stability of Cu/ZnO catalyst by hydrophobic treatment for low-temperature methanol synthesis from CO2

Abstract

CO2 hydrogenation to methanol is an efficient way to utilize CO2 and store hydrogen. However, realizing high activity and methanol selectivity as well as excellent stability are still challenges due to the competitive reverse water-gas shift (RWGS) reaction and the accumulation of water on the catalyst surface. Herein, Cu/ZnO catalyst was prepared by oxalic acid-assisted solid-state grinding method and then was subjected to hydrophobic treatment using stearic acid as a functionalization agent. The effect of stearic acid concentration on the physicochemical properties of Cu/ZnO catalysts and the catalytic activity for low-temperature CO2 hydrogenation to methanol was investigated and discussed in detail. Detailed catalyst characterizations disclosed that hydrophobic treatment using suitable concentration of stearic acid removed residues from the decomposition of oxalic acid and also increased specific surface area, surface basicity, reducibility and hydrogen adsorption strength on Cu/ZnO catalysts, leading to the enhanced catalytic performance and methanol selectivity. Among all the catalysts, Cu/Zn-2 mM catalyst exhibited methanol selectivity and methanol space time yield (STY) of 78.8% and 87.17 g/kg·h−1 at 200 ℃, much higher than those of untreated Cu/ZnO catalyst (71.7% and 68.93 g/kg·h−1). The hydrophobic Cu/Zn-2 mM catalyst also exhibited outstanding stability for low-temperature CO2 hydrogenation to methanol, keeping its activity for 100 h without obvious deactivation when compared to untreated Cu/ZnO catalyst. This facile hydrophobic treatment using stearic acid not also enhanced catalytic activity, methanol selectivity and stability of Cu/ZnO catalysts for low-temperature methanol synthesis, but also enlightened the invention of more hydrophobic materials in the near future.