Catalytic Oxidation of Soot and Volatile Organic Compounds over Cu and Fe Doped Manganese Oxides Prepared via Sol-Gel Synthesis
2021-24-0088
09/05/2021
- Features
- Event
- Content
- A set of manganese oxide catalysts was synthesized and doped with Cu and/or Fe by means of the citric acid sol-gel preparation method. The samples were studied by means of several characterization techniques: field-emission scanning electron microscopy (FESEM), X-ray powder diffraction (XRD), N2-physisorption at -196 °C, H2 and soot temperature-programmed reduction (H2-TPR, soot-TPR) and X-ray photoelectron spectroscopy (XPS). The catalytic performance of the prepared catalysts was investigated in the oxidation of a probe VOC molecule (propylene) and carbon soot singularly and simultaneously. The catalytic performances were studied as well assuring a content of 5 vol.% of water in the gaseous reactive mix. The investigations evidenced that the best soot catalytic oxidation rates occurred over the Mn2O3 sample, while the copper-doped manganese oxide (i.e. the MnCu15) showed the best performance in the decomposition of propylene. The soot conversion rates of the samples were positively correlated to the Mn3+/Mn2+ ratio of the samples, while the activity in the oxidation of propylene could be attributed to the reducibility enhancement caused by the insertion of Cu species in the structure of Mn2O3. The most active samples in soot oxidation demonstrated only a slight catalytic activity deactivation after thermal aging and practically no deactivation during the tests with humidity. Interestingly, the simultaneous soot-propylene oxidation tests evidenced an enhancement of the oxidation of soot particles in “tight” contact with the catalyst, likely due to a cooperative effect between soot and propylene oxidation.
- Pages
- 18
- Citation
- Marin Figueredo, M., Piumetti, M., Fino, D., Russo, N. et al., "Catalytic Oxidation of Soot and Volatile Organic Compounds over Cu and Fe Doped Manganese Oxides Prepared via Sol-Gel Synthesis," SAE Technical Paper 2021-24-0088, 2021, https://doi.org/10.4271/2021-24-0088.