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Silver-based catalytic materials for the simultaneous removal of soot and NOx

机译:同时去除烟灰和NOx的银基催化材料

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The potential of silver-based catalysts in the simultaneous removal of particulate matter (soot) and NO is investigated in this work and compared with that of a model Pt-Ba/Al2O3 catalyst. The Ag (5 wt%) - Ba (10 wt%)/MO (MO = CeO2, ZrO2, Al2O3) and Ag (5 wt%) - Sr (10 wt%)/CeO2 catalysts have been prepared by incipient wetness impregnation and characterized by BET, XRD, HRTEM, XPS and temperature-programmed reduction (TPR) experiments. The behavior of the catalyst in the soot combustion (under loose conditions) and NO removal has been separately analyzed by means of temperature programmed oxidation (TPO) and isothermal concentration step change (ICSC) experiments, respectively. The results show that all the catalysts are active in soot combustion with a significant decrease of oxidation onset temperature compared to uncatalyzed soot oxidation. The removal of NO in the absence and in the presence of soot was investigated under cycling conditions, i.e. alternating lean-rich phases according to the LNT strategy. It has been found that the Ag-based samples are able to simultaneously remove soot and NOR. In particular, comparing the behavior of the prepared catalysts, the Ba-containing systems showed higher NO storage capacity than Sr-catalyst; also, the nitrogen selectivity increased even if resulted lower than the traditional LNT Pt-based catalyst. A detrimental effect of soot on the NO storage activity has been also observed. (C) 2015 Elsevier B.V. All rights reserved.
机译:在这项工作中,研究了银基催化剂同时去除颗粒物(烟灰)和NO的潜力,并将其与模型Pt-Ba / Al2O3催化剂的潜力进行了比较。 Ag(5 wt%)-Ba(10 wt%)/ MO(MO = CeO2,ZrO2,Al2O3)和Ag(5 wt%)-Sr(10 wt%)/ CeO2催化剂是通过初湿浸渍和通过BET,XRD,HRTEM,XPS和程序升温还原(TPR)实验进行表征。分别通过程序升温氧化(TPO)和等温浓度阶跃变化(ICSC)实验分别分析了烟灰燃烧(在松散条件下)和NO去除过程中催化剂的行为。结果表明,与未催化的烟灰氧化相比,所有催化剂均在烟灰燃烧中具有活性,氧化开始温度显着降低。在循环条件下,即根据LNT策略,在交替的贫浓相中研究了在不存在和存在烟灰的情况下去除NO的方法。已经发现,基于Ag的样品能够同时去除烟灰和NOR。特别地,比较所制备的催化剂的行为,含Ba的体系显示出比Sr-催化剂更高的NO存储能力。同样,即使结果低于传统的LNT Pt基催化剂,氮的选择性也会提高。还观察到烟灰对NO储存活性的有害作用。 (C)2015 Elsevier B.V.保留所有权利。

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