4.5 Article

Improved catalytic activity and N-2 selectivity of Fe-Mn-O (x) catalyst for selective catalytic reduction of NO by NH3 at low temperature

Journal

RESEARCH ON CHEMICAL INTERMEDIATES
Volume 44, Issue 4, Pages 2703-2717

Publisher

SPRINGER
DOI: 10.1007/s11164-018-3255-x

Keywords

Fe-Mn-O-x; Selective catalytic reduction; N-2 selectivity; Fe-O-M-n species; Acid sites

Funding

  1. Natural Science Fund item of Yunnan Province [2013FD033]
  2. National Natural Science Foundation of China [21567030, 11447191]
  3. National Program on Key Basic Research Project of China (973 Program) [2014CB643404]

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FeO (x) , MnO (x) and Fe-Mn-O (x) catalysts were prepared by the co-precipitation method and used for the selective catalytic reduction (SCR) of NO (x) by NH3 at low temperature. Fe-Mn-O (x) catalyst showed the best catalytic activity and above 80% NO (x) conversion was obtained at 50-150 A degrees C. Nearly 80% N-2 selectivity of Fe-Mn-O (x) catalyst was acquired at the whole temperature range. The excellent low-temperature SCR activity and N-2 selectivity were ascribed to the abundant surface acid sites, the formation of Fe-O-Mn species, co-existence of multiple valence states (Mn4+, Mn3+ and Mn2+) and the proper redox ability. In addition, the interaction between Fe and Mn species over the Fe-Mn-O (x) catalyst was responsible for the improvement of SCR performance and N-2 selectivity. Fe-Mn-O (x) catalysts were prepared by the co-precipitation method and used for the selective catalytic reduction (SCR) of NO (x) by NH3 at low temperature. The formation of Fe-O-Mn species contributed to the co-existence of multiple valence states (Mn4+, Mn3+, Mn2+, Fe3+ and Fe2+), resulting in an increase in catalytic activity and N-2 selectivity. Besides, the abundance of acid sites was responsible for the superior N-2 selectivity. [GRAPHICS] .

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