Fe2O3 nanoparticles anchored in situ on carbon nanotubes via an ethanol-thermal strategy for the selective catalytic reduction of NO with NH3
Fe2O3 nanoparticles anchored in situ on carbon nanotubes via an ethanol-thermal strategy for the selective catalytic reduction of NO with NH3
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DOI：
10.1039/c4cy00789a
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发表时间：
2015
影响因子：
5
通讯作者：
Jinlong Han;Dengsong Zhang;P. Maitarad;Liyi Shi;Sixiang Cai;Hongrui Li;Lei Huang;Jian-ping Zhang-Jian-ping-Zha
中科院分区：
文献类型：
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作者：
Jinlong Han;Dengsong Zhang;P. Maitarad;Liyi Shi;Sixiang Cai;Hongrui Li;Lei Huang;Jian-ping Zhang-Jian-ping-Zha
Fe2O3 nanoparticles were anchored in situ on carbon nanotubes (CNTs) via an ethanol-thermal route, for the selective catalytic reduction (SCR) of NO with NH3. The structure and surface characteristics of the obtained catalysts were measured by transmission electron microscopy, X-ray diffraction, N2 adsorption–desorption isotherms, Raman, X-ray photoelectron spectroscopy, H2-temperature programmed reduction, and NH3-temperature programmed desorption. Compared with catalysts prepared via impregnation or co-precipitation methods, the synthesized catalyst showed better catalytic activity and a more extensive operating-temperature window. The TEM and XRD results suggested that the iron species was uniformly anchored on the surface of the CNTs. The Raman and XPS results indicated that the catalyst has a relatively higher number of defects, a higher atomic concentration of Fe present on the surface of the CNTs and a higher content of chemisorbed oxygen species. The H2-TPR and NH3-TPD results demonstrated that the catalyst possesses a more powerful reducibility and stronger acid strength than the other two catalysts. Based on the above-mentioned physicochemical properties, the obtained catalyst showed an excellent performance in the SCR of NO to N2 with NH3. Additionally, the catalyst also presented outstanding stability, H2O resistance and SO2 tolerance.
