Journal
CHEMOSPHERE
Volume 218, Issue -, Pages 895-906Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2018.11.131
Keywords
Hydrotalcite-derived oxides; KMnO4; Acetone and ethyl acetate; Catalytic oxidation
Categories
Funding
- National Key R&D Program of China [2016YFC0205300]
- National Engineering Laboratory for Mobile Source Emission Control Technology of China [NELMS2017A03]
- Natural National Science Foundation of China [21503144, 21690083]
- Tianjin Research Program of Application Foundation and Advanced Technique [15JCQNJC08500, 16JCQNJC05400]
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The MnOx was immobilized on the CoAl mixed oxides (CoAlO) derived from hydrotalcites with various anions (CO32-, Cl-, NO3- and SO42-) using the hydration and impregnation methods. The CoAIO oxides modified by KMnO4 were calcined in air at 300 degrees C to obtain stable oxides, which could be used as catalysts for VOCs (acetone and ethyl acetate) oxidation. CoAlO with CO32- and 30 h of hydration time (CoAlO-C-Mn-30) exhibited a promising catalytic activity (T-90 = 173 degrees C for acetone oxidation; T-90 = 175 degrees C for ethyl acetate), highly superior to CoAlO without KMnO4 modification. The improvement in acetone and ethyl acetate catalytic oxidation was ascribed to the Co3+ and surface adsorbed oxygen species. The increase of Co3+ in the CoAlO-C-Mn-30 oxide thanked to the self-decomposition of KMnO4 and reducibility of Co2+ in the CoAlO oxide during the hydration process. This was also confirmed by XRD and XPS characterization, which showed that Mn cations were enriched on the catalyst surface in the valences of +3 and +4. The catalytic activity of the catalyst remained unchanged in four cycles in the presence of 5.5 vol.% water vapor, which indicated a great potential for industrial application. (C) 2018 Elsevier Ltd. All rights reserved.
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