Alkali and Phosphorus Resistant Zeolite-like Catalysts for NOx Reduction by NH3

被引:83
|
作者
Yan, Lijun [1 ]
Ji, Yunyun [1 ]
Wang, Penglu [1 ]
Feng, Chong [1 ]
Han, Lupeng [1 ]
Li, Hongrui [1 ]
Yan, Tingting [1 ]
Shi, Liyi [1 ]
Zhang, Dengsong [1 ]
机构
[1] Shanghai Univ, Res Ctr Nano Sci & Technol, State Key Lab Adv Special Steel, Sch Environm & Chem Engn,Dept Chem,Coll Sci, Shanghai 200444, Peoples R China
基金
国家重点研发计划; 中国博士后科学基金; 中国国家自然科学基金;
关键词
IN-SITU DRIFTS; NH3-SCR REACTION; MECHANISM; PERFORMANCE; OXIDES; PROTECTION; POTASSIUM; NANOTUBES; CU-SSZ-13; H3PW12O40;
D O I
10.1021/acs.est.0c03290
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
At present, the deactivation of selective catalytic reduction (SCR) catalysts caused by the coexistence of alkali metal and phosphorus (P) remains an urgent problem and lacks corresponding strategies against catalyst poisoning. Herein, a novel zeolite-like Ce-Si5Al2Ox catalyst derived from an ultrasmall nanozeolite EMT precursor was synthesized without organic templates at ambient temperature. This catalyst was able to maintain above 95% NOx conversion in the 270-540 degrees C temperature range. Moreover, 1 wt % potassium (K) and 5 wt % P loading had no influence on the SCR performance of the Ce-Si5Al2Ox catalyst at 300-480 degrees C. It was demonstrated that cerium (Ce) was highly dispersed in the amorphous aluminum (Al) silicate derived from EMT zeolites and expressed high catalytic performance. Besides, a large number of acid sites were reserved to absorb ammonia allowing effective participation in the SCR reaction and capturing alkali metals, thus improving the SCR performance and K resistance. Additionally, the strong interaction between Ce and aluminosilicate decreased cerium phosphate production, preventing deactivation of the catalysts. Thus, this novel low-cost zeolite-like Ce-Si5Al2Ox catalyst with a highly active ion-exchanged metal phase and abundant surface acid sites paves a way for designing new efficient and poisoning-resistant SCR catalysts for practical applications.
引用
收藏
页码:9132 / 9141
页数:10
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