Remarkable enhancement of the selective catalytic reduction of NO at low temperature by collaborative effect of ethanol and NH3 over silver supported catalyst

被引:40
作者
Barreau, M. [1 ]
Tarot, M-L. [1 ]
Duprez, D. [1 ]
Courtois, X. [1 ]
Can, F. [1 ]
机构
[1] Univ Poitiers, CNRS, Inst Chim Milieux Mat Poitiers IC2MP, UMR 7285, 4 Rue Michel Brunet,TSA 51106, F-86073 Poitiers 9, France
关键词
NOx; SCR; Ethanol; NH3; AG/AL2O3; CATALYSTS; SURFACE-PROPERTIES; ALUMINA CATALYST; H-2-ASSISTED SCR; NITROGEN-OXIDES; GAMMA-ALUMINA; MECHANISM; AMMONIA; SPECTROSCOPY; HYDROGEN;
D O I
10.1016/j.apcatb.2017.08.015
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 NOx selective catalytic reduction (SCR) is extensively studied as an effective process for air pollutants abatement from lean burn and Diesel vehicles. In the implemented Urea-SCR technology, the NO2/NOx ratio is a key parameter that limits the deNO(x) efficiency at low temperature (175-250 degrees C). We demonstrate that co-feeding of ammonia and ethanol on a Ag/Al2O3 catalyst enables a drastic enhancement of the NOx conversion at temperatures below 200 degrees C using only NO as NOx (standard SCR condition). Even if NO2 is provided at low temperature by the NO oxidation over Ag/Al2O3 in presence of EtOH, the NO. conversion improvement is not only due to a direct reaction between NH3 and NOx, but mainly attributed to the availability of hydrogen H* species resulting from EtOH oxidation (similar to a H-2 assisted NH3-SCR process). Due to the presence of remaining NH3 and NO2 (formed over Ag/Al2O3 catalyst), further deNO(x) efficiency improvement was obtained at low temperature by addition of a NH3-SCR catalyst (WO3/CeZr). The critical dependence of the SCR process on the Diesel Oxidation Catalyst (DOC) efficiency at low temperature is thus avoided. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:19 / 30
页数:12
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