Effect of Cu content on the catalytic activity of CuSiBEA zeolite in the SCR of NO by ethanol: Nature of the copper species

被引:74
|
作者
Janas, Janusz [2 ]
Gurgul, Jacek [2 ]
Socha, Robert P. [2 ]
Dzwigaj, Stanislaw [1 ,3 ]
机构
[1] Univ Paris 06, UMR 7197, Lab React Surface, F-75252 Paris 05, France
[2] Polish Acad Sci, Inst Catalysis & Surface Chem, PL-30239 Krakow, Poland
[3] CNRS, UMR 7197, Lab React Surface, F-75252 Paris 05, France
关键词
SiBEA zeolite; Copper; NO; Ethanol; XRD; DR UV-vis-NIR; XPS; Catalysis; X-RAY PHOTOELECTRON; SELECTIVE REDUCTION; FE-ZSM-5; CATALYSTS; CU-ZSM-5; EXCHANGED ZSM-5; NITROGEN-OXIDES; BEA ZEOLITE; METAL-IONS; DECOMPOSITION; SPECTROSCOPY;
D O I
10.1016/j.apcatb.2009.05.028
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
The effect of Cu content on the catalytic activity of Cu(x)SiBEA zeolites in the selective catalytic reduction (SCR) of NO by ethanol is investigated, The Cu(x)SiBEA zeolites (x = 0.3, 1.5 and 3.3 Cu wt%) are prepared by a two-step postsynthesis method which allows to control the introduction of copper into BEA zeolite and thus to obtain catalysts with isolated tetrahedral Cu(II) species. The incorporation of Cu into the vacant T-sites of SiBEA framework is evidenced by XRD. The presence of isolated tetracoordinated Cu(II) as the main copper species is evidenced by DR UV-vis and XPS investigations. Cu(03)SiBEA, Cu(1.5)SiBEA and Cu(3.3)SiBEA with isolated Cu(II) species are active in SCR of NO by ethanol with the maximum No conversion of 33%, 45.5% and 50% and selectivity towards N-2 Of 90%. 97% and 75%, respectively. These results indicate that activity of Cu,SiBEA in the SCR process increases with Cu content and the main reaction route is the reduction of NO toward N-2. The decreases of selectivity toward N-2 and increases toward NO2 with Cu content, is probably related to formation of small amount of octacoordinated Cu(II) as suggested by XPS data. A possible pathway for the formation of tetracoordinated Cu(II) in the framework of Cu(x)SiBEA is proposed. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:217 / 224
页数:8
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