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Manganese oxide nanorod catalysts for low-temperature selective catalytic reduction of NO with NH(3)

MnO(x) nanorod catalysts were successfully synthesized by two different preparation methods using porous SiO(2) nanorods as the template and investigated for the low-temperature selective catalytic reduction (SCR) of NO with NH(3). The catalysts were characterized by scanning electron microscopy, tr...

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Detalles Bibliográficos
Autores principales: Wang, Yifan, Wang, Yanli, Kong, Zhenkai, Kang, Ying, Zhan, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9180140/
https://www.ncbi.nlm.nih.gov/pubmed/35755592
http://dx.doi.org/10.1039/d1ra06758c
Descripción
Sumario:MnO(x) nanorod catalysts were successfully synthesized by two different preparation methods using porous SiO(2) nanorods as the template and investigated for the low-temperature selective catalytic reduction (SCR) of NO with NH(3). The catalysts were characterized by scanning electron microscopy, transmission electron microscopy, nitrogen adsorption, X-ray diffraction, X-ray photoelectron spectroscopy, and NH(3) temperature-programmed desorption. The results show that the obtained MnO(x)-P nanorod catalyst prepared by redox precipitation method exhibits higher NO removal activity than that prepared by the solvent evaporation method in the low temperature range of 100–180 °C, where about 98% NO conversion is achieved over MnO(x)(0.36)-P nanorods. The reason is mainly attributed to MnO(x)(0.36)-P nanorods possessing unique flower-like morphology and mesoporous structures with high pore volume, which facilitates the exposure of more active sites of MnO(x) and the adsorption of reactant gas molecules. Furthermore, there is a lower crystallinity of MnO(x), higher percentage of Mn(4+) species and a large amount of strong acid sites on the surface. These factors contribute to the excellent low-temperature SCR activity of MnO(x)(0.36)-P nanorods.