Understanding deNOx mechanisms in transition metal exchanged zeolites

被引:3
|
作者
Nasir, Jamal Abdul [1 ]
Beale, Andrew M. [1 ,2 ]
Catlow, C. Richard A. [1 ,2 ,3 ]
机构
[1] UCL, Dept Chem, 20 Gordon St, London WC1H 0AJ, England
[2] Rutherford Appleton Lab, UK Catalysis Hub, Res Complex Harwell, R92, Harwell OX11 0FA, Oxfordshire, England
[3] Cardiff Univ, Cardiff Catalysis Inst, Sch Chem, Cardiff CF10 3AT, Wales
基金
英国工程与自然科学研究理事会;
关键词
SELECTIVE CATALYTIC-REDUCTION; NITROUS-OXIDE DECOMPOSITION; ISOLATED CU2+ IONS; X-RAY-ABSORPTION; ACTIVE-SITES; NOX REDUCTION; NITRIC-OXIDE; HYDROTHERMAL STABILITY; CU/SAPO-34; CATALYSTS; NH3-SCR CATALYSTS;
D O I
10.1039/d3cs00468f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition-metal-containing zeolites have wide-ranging applications in several catalytic processes including the selective catalytic reduction (SCR) of NOx species. To understand how transition metal ions (TMIs) can effect NOx reduction chemistry, both structural and mechanistic aspects at the atomic level are needed. In this review, we discuss the coordination chemistry of TMIs and their mobility within the zeolite framework, the reactivity of active sites, and the mechanisms and intermediates in the NH3-SCR reaction. We emphasise the key relationship between TMI coordination and structure and mechanism and discuss approaches to enhancing catalytic activity via structural modifications.
引用
收藏
页码:11657 / 11691
页数:35
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