Performance of K and Ni substituted La1-xKxCo1-yNiyO3-δ perovskite catalysts used for soot combustion, NOx storage and simultaneous NOx-soot removal

被引:51
作者
Li, Zhaoqiang [1 ]
Meng, Ming [1 ]
Dai, Fangfang [1 ]
Hu, Tiandou [2 ]
Xie, Yaning [2 ]
Zhang, Jing [2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin Key Lab Appl Catalysis Sci & Engn, Tianjin 300072, Peoples R China
[2] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Soot combustion; NOx storage and reduction; Perovskite; K; Ni; DIESEL SOOT; OXIDATION;
D O I
10.1016/j.fuel.2011.10.040
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The nanometric substituted perovskite catalysts La1-xKxCo1-yNiyO3-delta (x = 0, 0.1; y = 0, 0.05, 0.1) were synthesized by citric acid complexation method, and employed for soot combustion, NOx storage and simultaneous NOx-soot removal. Their structures and physico-chemical properties were characterized by XRD, EXAFS, BET, SEM, H-2-TPR, and XPS techniques. When K and Ni are simultaneously introduced into LaCoO3 catalyst, soot combustion is largely accelerated, with the temperature (T-m) for maximal soot conversion lowered by at least 50 degrees C; moreover, NOx reduction by soot is also facilitated. The La0.9K0.1Co0.95Ni0.05O3-delta catalyst exhibits not only the lowest T-m (367 degrees C) temperature but also the highest soot combustion rate (67.3 mu g/s g catalyst). Meanwhile, the NOx reduction percentage over this catalyst can reach 21%. The kinetic results show that the activation energy for soot combustion over La0.9K0.1Co0.95Ni0.05O3-delta (81.34 kJ mol(-1)) is much lower than that over LaCoO3 (107.7 kJ mol(-1)). The H-2-TPR and XPS results show that the La0.9K0.1Co0.95Ni0.05O3-delta catalyst possesses better redox properties, more tetravalent cobalt ions and larger amount of surface adsorbed oxygen species, which determines its novel performance for soot combustion, NOx storage and soot-NOx removal. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:606 / 610
页数:5
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