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Updated: May 25, 2025

Temperature-programmed Deoxygenation of Acetic Acid on Molybdenum Carbide Catalysts
Published on: February 7, 2017
Stoichiometric Selective Carbonylation of Methane to Acetic Acid by Chemical Looping
Yinghao Wang1, Chunyang Dong1,2, Mariya Shamzhy3
1UCCS-Unité de Catalyse et Chimie du Solide, Université de Lille, CNRS, Centrale Lille, ENSCL, Université d'Artois, UMR, 8181 Lille, France.
Abstract:
The conversion of methane to valuable products is one of the main challenges of modern chemistry. Acetic acid (AcOH) is a key chemical reagent in industry, produced nowadays by the carbonylation of methanol over homogeneous Rh and Ir catalysts. Here, we propose a stepwise chemical looping approach for the highly selective stoichiometric synthesis of AcOH by carbonylation of methane with CO using single-site Pt over isolated phosphotungstic anions on a titania support (Pt-HPW-TiO2). The reaction proceeds by methane activation, which coincides with the reduction of initially oxidized Pt species in the presence of CO at 423 K and results in surface acetates attached to TiO2. Subsequent hydrolysis by water at ambient temperature results in the synthesis of AcOH in a stoichiometric amount corresponding to 1.5 Pt. Spent Pt-HPW-TiO2 is restored to the initial state by subsequent calcination in air. This approach provides an opportunity for the selective synthesis of AcOH (>99% in liquid phase) from methane, carbon monoxide, and air. A high concentration of AcOH (1.1 wt %) in an aqueous solution can be obtained at a high conversion of methane (4.5%).
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