Zeolite physical mixing restores the high temperature NH3-SCR of CeO2: The crucial role of NOx activation

被引:0
作者
Zhou, Qinyu [1 ]
Tan, Chong [1 ]
Tang, Tianfa [1 ]
Wang, Yu [1 ]
Li, Siyuan [1 ]
Tao, Meilin [1 ,2 ]
Zhang, Hongliang [3 ,4 ]
Yang, Liu [1 ,2 ]
Tang, Changjin [1 ,2 ]
机构
[1] Nanjing Normal Univ, Sch Environm, Nanjing 210023, Peoples R China
[2] Jiangsu Prov Engn Res Ctr Environm Risk Prevent &, Nanjing 210023, Peoples R China
[3] Anhui Univ Technol, Key Lab Met Emiss Reduct & Resources Recycling, Minist Educ, Maanshan 243002, Peoples R China
[4] Anhui Univ Technol, Anal & Testing Cent Facil, Maanshan 243002, Peoples R China
关键词
High-temperatureNH3-SCR; NH3; over-oxidation; NO activation; CeO2; ZSM-5; SELECTIVE CATALYTIC-REDUCTION; OXIDATION; AMMONIA; OXIDES; NH3; CERIA; PERFORMANCE; STABILITY; MECHANISM; PROMOTION;
D O I
10.1016/j.seppur.2025.133009
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The occurrence of NH3 over-oxidation represents one intractable challenge for the effective application of NH3-SCR technology. Herein, a rational NOx activation strategy was innovatively proposed to counteract NH3 over oxidation during high temperature NH3-SCR. As a proof of concept, the hybrid catalyst of CeO2-ZSM-5 was explored. It was shown that the activity of CeO2 in NH3-SCR was profoundly improved via physically mixing with ZSM-5, achieving more than 85 % NO at 500 degrees C, in sharp contrast to the negative NO conversion present for pristine CeO2. Comprehensive characterizations from NH3-TPD, NO-TPD and in situ DRIFTS verified the negligible modification of NH3 oxidation but significant alteration of surface NOx. Due to the facile NOx activation, the reaction of NH3 + NOx overwhelms that of NH3 + O2, leading to the obtainment of excellent high temperature NH3-SCR performance. The novel strategy reported here is expected to provide valuable guidance for designing NH3-SCR catalysts with superior high temperature performance.
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页数:9
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