Abstract

In this work, the thermal stability and catalytic activity of Fe2O3 catalyst for Hg0 oxidation were improved by the introduction of CeO2 and Pt. During high-temperature calcination at 400 °C, the mesoporous structure of Pt/CeO2/Fe2O3 remained stable, and it also retained higher specific surface area and lower average pore size than Fe2O3. The X-ray diffraction, transmission electron microscopy, and thermal gravimetric-differential scanning calorimetry results revealed that the modification of CeO2 and Pt retarded the crystallization and growth of Fe2O3 grains during high-temperature calcination, limiting Fe2O3 particles to a smaller size. Temperature-programmed desorption experiments showed that Hg0 adsorption of Pt/CeO2/Fe2O3 was promoted. In addition, X-ray photoelectron spectroscopy spectra suggested that adding CeO2 and Pt also increased the content of chemisorbed oxygen and transformed Fe2O3 into an electron-rich state, which consequently improved its catalytic performance for Hg0 oxidation.

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