Rare‐earth Yttrium Exchanged Cu‐SSZ‐39 Zeolite with Superior Hydrothermal Stability and SO<sub>2</sub>‐Tolerance in NH<sub>3</sub>‐SCR of NO<i>x</i>
Rui Yu, Haiyu Kong, Zhenchao Zhao, Chuan Shi, Xiangju Meng, Feng‐Shou Xiao, Trees De Baerdemaeker, Andrei‐Nicolae Parvulescu, Ulrich Müller, Weiping Zhang
Abstract
Abstract With the increasingly stringent restrictions on engine exhaust gases, efforts to enhance the activity, hydrothermal stability, and SO 2 ‐tolerance of NH 3 ‐SCR catalysts are highly desirable and challenging. Here, we present the concept of controlled sitings of the metal active sites by modifying Cu‐SSZ‐39 with yttrium (Y) as the rare‐earth metal for enhanced NH 3 ‐SCR performances. Cu(0.25)‐Y(0.12)‐AEI(10) shows superior NO x conversion even after harsh hydrothermal aging at 900 °C, conditions under which standard Cu‐AEI cannot withstand. After long‐term SO 2 poisoning, Cu(0.25)‐Y(0.12)‐AEI(10) shows a significantly higher NO x conversion than both Cu‐AEI and conventional Cu‐CHA. The structure‐activity correlation obtained from multiple characterizations, kinetics analyses and DFT calculations reveal that the Y ions act to inhibit dealumination during hydrothermal aging, as a sacrificial agent for SO 2 ‐poisoning, and to stabilize catalytically active Cu centers within the zeolite framework. This synthesis concept provides insight into design of more stable and active NH 3 ‐SCR catalysts in future.