SO2- and H2O-Tolerant Catalytic Reduction of NOxat a LowTemperature via Engineering Polymeric VOxSpecies by CeO2

被引:67
作者
Hu, Weiwei [1 ]
He, Jiebing [1 ]
Liu, Xiangyu [1 ]
Yu, Huijun [1 ]
Jia, Xinyu [1 ]
Yan, Tingting [1 ]
Han, Lupeng [1 ]
Zhang, Dengsong [1 ]
机构
[1] Shanghai Univ, Coll Sci, Res Ctr Nano Sci & Technol, Dept Chem,Int Joint Lab Catalyt Chem,State Key La, Shanghai 200444, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
air pollution control; environmental catalysis;   selective catalytic reduction; NOxreduction; SO(2)tolerance; H2O tolerance; IN-SITU DRIFTS; LOW-TEMPERATURE NH3-SCR; ACTIVE-SITES; NO; NH3; SCR; PERFORMANCE; OXIDE; RESISTANCE; TIO2;
D O I
10.1021/acs.est.1c08715
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Selective catalytic reduction (SCR) of NOxoverV2O5-based oxide catalysts has been widely used, but it is still achallenge to efficiently reduce NOxat low temperatures under SO2and H2O co-existence. Herein, SO2- and H2O-tolerant catalyticreduction of NOxat a low temperature has been originallydemonstrated via engineering polymeric VOxspecies by CeO2. Thepolymeric VOxspecies were tactfully engineered on Ce-V2O5composite active sites via the surface occupation effect of Ce, andthe obtained catalysts exhibited remarkable low-temperatureactivity and strong SO2and H2O tolerance at 250 degrees C. The stronginteraction between Ce and V species induced the electron transferfrom V to Ce and tuned the SCR reaction via the E-R pathwaybetween the NH4+/NH3species and gaseous NO. In the presence of SO2and H2O, the polymeric VOxspecies had not been hardlyinfluenced, while the formation of sulfate species on Ce sites not only promoted the adsorption of NH4+species and the reactionbetween gaseous NO and NH4+but also facilitated the decomposition of ammonium bisulfate through weakening the strong bondbetween HSO4-and NH4+. This work provided a new strategy for SO2- and H2O-tolerant catalytic reduction of NOxat a lowtemperature.
引用
收藏
页码:5170 / 5178
页数:9
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