Substitution of WO3 in V2O5/WO3–TiO2 by Fe2O3 for selective catalytic reduction of NO with NH3
Substitution of WO3 in V2O5/WO3–TiO2 by Fe2O3 for selective catalytic reduction of NO with NH3
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DOI:
10.1039/c2cy20383a
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发表时间:
2012-12
影响因子:
5
通讯作者:
Shijian Yang;Chizhong Wang;Lei Ma;Yue Peng;Zan Qu;N. Yan;Jinghuan Chen;Huazhen Chang;Junhua Li
中科院分区:
文献类型:
--
作者:
Shijian Yang;Chizhong Wang;Lei Ma;Yue Peng;Zan Qu;N. Yan;Jinghuan Chen;Huazhen Chang;Junhua Li
To improve N2 selectivity and lower the cost, WO3 in V2O5/WO3–TiO2 was substituted by a low cost composition Fe2O3 for selective catalytic reduction (SCR) of NO with NH3. The SCR reaction over V2O5/Fe2O3–TiO2 mainly followed the Eley–Rideal mechanism (i.e. the reaction between activated ammonia species and gaseous NO). There were two active components on V2O5/WO3–TiO2 for the activation of adsorbed NH3 (i.e. V5+ and Fe3+). The acid sites on V2O5/Fe2O3–TiO2 mainly resulted from the support Fe2O3–TiO2, so the adsorbed NH3 preferred to be activated by Fe3+ rather than by V5+. V5+ on V2O5/Fe2O3–TiO2 could accelerate the regeneration of Fe3+ on Fe2O3–TiO2 due to the rapid electron transfer between V5+ and Fe2+ on the surface, so the activation of adsorbed NH3 by Fe3+ was promoted. As some NH3 adsorbed on V2O5/Fe2O3–TiO2 was not activated by Fe3+, the inactivated NH3 could then be activated by V5+ on the surface. As a result, 2% V2O5/Fe2O3–TiO2 showed excellent SCR activity, N2 selectivity and H2O/SO2 durability at 300–450 °C. Furthermore, the emission of 2% V2O5/Fe2O3–TiO2 to the fly ash can be prevented by an external magnetic field due to its inherent magnetization. Therefore, 2% V2O5/Fe2O3–TiO2 could be a promising low-cost catalyst in NO emission control.