催化作用
热液循环
氮氧化物
化学吸附
烧结
物理吸附
X射线光电子能谱
化学工程
化学
氧气
降级(电信)
材料科学
无机化学
冶金
物理化学
有机化学
燃烧
计算机科学
工程类
电信
作者
Beom‐Sik Kim,Hojin Jeong,Junemin Bae,Pyung Soon Kim,Chang Hwan Kim,Hyunjoo Lee
标识
DOI:10.1016/j.apcatb.2020.118871
摘要
A combination of the Pt-BaO/CeO2 and Cu/CeO2 (PBC + CC) catalyst offers high NOx storage and reduction (NSR) performance at low temperatures; however, the PBC + CC catalyst is prone to deactivation upon hydrothermal aging. In this study, we used a reduced γ-Al2O3 support with unsaturated penta-coordinated Al3+ sites, which can anchor catalytic materials (Pt, Cu, BaO, and CeO2). The physical mixture of Pt-BaO-CeO2 and Cu-CeO2 deposited on the reduced Al2O3 (PBCrA + CCrA) was prepared and tested for the NOx removal. The PBCrA + CCrA catalyst showed little degradation after hydrothermal aging at 750 °C. XRD, HR-TEM, CO chemisorption, N2O chemisorption, and N2 physisorption results showed that catalytically active phases were barely changed even after the hydrothermal aging, particularly preventing ceria sintering. CO-TPR and XPS results demonstrated that the PBCrA + CCrA catalyst has a superior reducibility of lattice oxygen on CeO2, leading to excellent low-temperature activity.
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