NO selective reduction by hydrogen on potassium titanate supported palladium catalyst

被引:52
|
作者
Li, Landong [1 ,2 ]
Zhang, Fuxiang [1 ]
Guan, Naijia [1 ]
Schreier, Ellen [3 ]
Richter, Manfred [3 ]
机构
[1] Nankai Univ, Inst New Catalyt Mat Sci, Coll Chem, Tianjin 300071, Peoples R China
[2] Chinese Acad Sci, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R China
[3] Leibniz Inst Catalysis, Branch Berlin, D-12489 Berlin, Germany
基金
中国国家自然科学基金;
关键词
palladium; titanate; hydrogen; NO reduction;
D O I
10.1016/j.catcom.2008.02.019
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Potassium titanate (K2O-6TiO(2)) nanowires were successfully prepared by alkali treatment of TiO2 (79% anatase, 21% rutile) under autogenous pressure in a Teflon-lined autoclave at 200 degrees C. After further modification with 1 wt.% Pd by wet impregnation, the calcined and pre-reduced Pd/K2O-6TiO(2) catalyst was applied for selective reduction of NOx by H-2 (H-2-SCR) under lean conditions, together with Pd/Al2O3 and Pd/TiO2 as reference. The reference catalysts exhibited maximum NO conversion of about 50-60% at 100-130 degrees C, but with low N-2 selectivity. The N-2 selectivity on Pd/K2O-6TiO(2) was considerably high, reaching 80% at maximum, with only 11% conversion of the admixed hydrogen reductant. In situ DRIFT spectroscopy revealed surface-fixed nitrates and Pd-bound NO, but no NHx ad-species. It is concluded, that the beneficial effect of the K2O-6TiO(2) support is due mainly to a stabilization of high Pd dispersion with enhanced concentration of Pd-0-NO intermediates, and due to support alkalinity, that enhances nitrate fixation. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1827 / 1832
页数:6
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