Palladium catalysts supported on sulfated ceria-zirconia for the selective catalytic reduction of NOx by methane: Catalytic performances and nature of active Pd species

被引:18
作者
Azambre, B. [1 ]
Zenboury, L. [1 ]
Da Costa, P. [2 ]
Capela, S. [3 ]
Carpentier, S. [3 ]
Westermann, A. [1 ]
机构
[1] Univ Paul Verlaine Metz, IUT Chim, LCME, Inst Jean Barriol, F-57500 St Avold, France
[2] Univ Paris 06, Inst Jean Le Rond Alembert, CNRS, UMR 7190, F-78210 St Cyr Lecole, France
[3] CRIGEN, GDF SUEZ, F-93211 St Denis, France
关键词
No-x; CexZr1-xO2; CH4-SCR; Sulfates; NO2; CO adsorption; Palladium; NITRIC-OXIDE; SURFACE; SCR; CH4; CO; HYDROCARBONS; ADSORPTION; EXCESS; O-2; TGA;
D O I
10.1016/j.cattod.2010.12.026
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Novel Pd sulfated ceria-zirconia catalysts for the SCR of NOx by methane were prepared by impregnation of a PdCl2 precursor dissolved in ammonia solution on a sulfated Ce0.21Zr0.79O2 support, itself obtained by direct sulfation of a ceria-zirconia nanopowder in 0.5 M H2SO4. Best CH4-SCR performances under the conditions 150 ppm NO; 1500 ppm CH4; 7 vol.% O-2 were achieved using Pd loadings in the range 0.24-0.53 wt.% with 30-35% NO conversion to N-2 around 350-400 degrees C. By contrast, the formation of a PdOx phase at superior Pd loadings was found detrimental for the SCR activity because it promotes also the non-selective methane oxidation. Increasing CH4 concentrations or adding H2O to the feed have opposite trends on DeNO(x), activity, the latter being detrimental at low-medium temperatures due to inhibiting effects on adsorption. As evidenced by DRIFTS of CO and pyridine adsorption, UV-Vis, HRTEM-EDX and XRD, the nature of the Pd species active in SCR could be [Pd(O)-H](x+) isolated species and/or small [(PdO)(n)-H](x+) clusters possessing a high Lewis acidity and a low reducibility. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:242 / 249
页数:8
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