Fabrication of MnO-CeO/cordierite catalysts doped with FeO and CuO for preferable catalytic oxidation of chlorobenzene.

Environ Technol

Jiangsu Collaborative Innovation Center of Atmospheric Environment and Equipment Technologies, Jiangsu Key Laboratory of Atmospheric Environmental Monitoring & Pollution Control, School of Environmental Science & Engineering, Nanjing University of Information Science & Technology, Nanjing, People's Republic of China.

Published: May 2020

AI Article Synopsis

  • MnO-CeO catalysts doped with metals like Cu, Fe, Co, and La demonstrated effective catalytic oxidation of chlorobenzene when supported on cordierite.
  • The properties of these catalysts varied significantly based on the different molar ratios of Mn/Ce and M/Mn, which were analyzed using various characterization techniques.
  • CuO-MnO-CeO catalysts showed superior chlorobenzene conversion with a light-off temperature around 400°C, while FeO-MnO-CeO catalysts produced more carbon monoxide due to incomplete oxidation; both types remained stable without deactivation at high temperatures.

Article Abstract

A series of MnO-CeO catalysts with MO doping (M = Cu, Fe, Co and La) supported on cordierite were synthesized by the citric acid complex method, showing preferable catalytic oxidation of chlorobenzene. The distribution of active oxides, surface areas, as well as the structural morphology of M-MnO-CeO catalysts varied with the different Mn/Ce and M/Mn molar ratios. Meanwhile, physicochemical properties of these catalysts were characterized by XRD, BET, SEM, TEM, H-TPR and IR. More importantly, the catalytic oxidation routes were also investigated where the process was from chlorobenzene to CO, HO, HCl and other by-products for the FeO-MnO-CeO and CuO-MnO-CeO catalysts. The CuO-MnO-CeO catalysts showed a higher chlorobenzene conversion, and the measured light-off temperature was approximately 400°C. However, a large amount of chloropropane as main by-products was observed. For the FeO-MnO-CeO catalysts, more carbon monoxide could be found with inadequate oxidation. Comparative analyses of two catalysts indicated that the main cause of the oxidation activities and mechanisms were different in the oxidation capacity and water absorbability of FeO and CuO. Nevertheless, all of these catalysts did not exhibit any deactivation due to chloride with a high reaction temperature, with chloride transformed to form HCl in the off-gas stream.

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Source
http://dx.doi.org/10.1080/09593330.2018.1543359DOI Listing

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