Abstract
Reforming of acetic acid was investigated on Rh supported on CeO2–ZrO2 modified with 3 wt % La. The active catalyst converted acetic acid to H2-rich gas and hardly formed coke. The low rate of coke formation is concluded to be related to the presence of redox-active oxygen limiting the concentration of coke precursors. Temperature-programmed 18O2 isotope exchange measurements showed that the La2O3 and Rh enhanced the mobility of lattice oxygen compared with that of the parent CeO2–ZrO2. Ketonization and decarboxylation of acetic acid are the dominating reactions over the latter up to 600 °C, whereas above 600 °C, steam reforming and water gas shift also contribute. Over 0.5 wt % Rh on La2O3/CeO2–ZrO2, reforming and water gas shift reactions dominate, even below 300 °C, producing mostly H2 and CO2. Using isotope labeling, it is shown that acetic acid adsorbs dissociatively on Rh, forming acetates, which sequentially decarboxylate and form surface methyl groups. The latter are in turn converted to CO, CO2, ...
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