金红石
锐钛矿
催化作用
氧化还原
初湿浸渍
X射线光电子能谱
热稳定性
材料科学
氧气
吸附
兴奋剂
无机化学
化学工程
化学
物理化学
选择性
有机化学
光电子学
光催化
工程类
作者
Wenzhe Si,Haiyan Liu,Tao Yan,Hui Wang,Chi Fan,Shangchao Xiong,Ziqi Zhao,Yue Peng,Jianjun Chen,Junhua Li
标识
DOI:10.1016/j.apcatb.2020.118797
摘要
Sn-doped rutile TiO2 supports (SnxTi1−xO2, X = 0.1, 0.2, 0.5) were designed and V2O5/SnxTi1−xO2 catalysts were synthesized by incipient wetness impregnation. The V2O5/Sn0.2Ti0.8O2 exhibited higher low-temperature SCR activity and better H2O and SO2 resistance than the traditional V2O5/TiO2 (anatase) catalyst. In situ DRIFTs, XPS, H2-TPR and NH3/NO+O2-TPD results showed that Sn doping improved the redox property, NH3/NO adsorption and the amount of surface chemisorbed oxygen. The kinetic study indicated that Sn doping had little effect on SCR reaction pathways, but promoted SCR reaction, mainly through Eley-Rideal mechanism. More importantly, the V2O5/Sn0.2Ti0.8O2 showed better thermal stability than V2O5/TiO2. For V2O5/TiO2, the aggregation and sintering of the catalyst occurred, and the surface area decreased significantly after thermal aging. The monomeric vanadyl species partially transferred to crystalline V2O5. But for V2O5/Sn0.2Ti0.8O2, the surface area did not decrease as much as that for V2O5/TiO2, and the monomeric vanadyl species partially transferred to the polymeric vanadyl species.
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