催化作用
气凝胶
氧化还原
纳米孔
无机化学
化学
物理吸附
氧气
选择性催化还原
氨
色散(光学)
比表面积
硫酸盐
化学工程
材料科学
纳米技术
有机化学
物理
工程类
光学
作者
Jihène Arfaoui,Abdelhamid Ghorbel,Carolina Petitto,Gérard Delahay
标识
DOI:10.1016/j.inoche.2022.109494
摘要
Selective catalytic reduction (SCR) of nitrogen oxide (NO) by ammonia (NH3) was studied in this work over new sulfate (SO42-) or tungsta (WO3) modified CeO2-TiO2 aerogel catalysts. The catalytic systems were elaborated via sol gel method then characterized by: XRD, N2-Physisorption at 77 K, DRUV–vis, NH3-TPD and H2-TPR. It was revealed that the nature of acidic components influences differently the texture, surface oxygen concentration, acidity, reducibility and NH3-SCR activity of new Ce-based catalysts. Hence, the incorporation of sulfate modifies the nature of Ce species, improves their dispersion through the Ce-SO42- interactions and, particularly, generates new strong acid sites which display superior catalytic performance at high temperature NO reduction (NO conversion into N2 > 90 % between 450 and 500 °C over CeO2-TiO2-SO42- catalyst). However, the addition of tungsta affects slightly the surface acidity of CeO2-TiO2 catalyst but it induces the creation of more reactive surface oxygen and new redox sites at its surface (mainly due to the existence of W-Ce interactions) leading to highly active WO3-CeO2-TiO2 system for the low temperature NH3-SCR reaction with above 90 % NO conversion into N2 between 320 and 400 °C.
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