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Oxidation of nitric oxide to nitrogen dioxide over Ru catalysts

机译:在Ru催化剂上将一氧化氮氧化为二氧化氮

摘要

A series of TiO(2) supported catalysts were prepared by impregnation method in a rotary evaporator and evaluated for the oxidation of NO to NO(2). Among all catalysts studied, Ru/TiO(2) catalyst exhibited the best activity and a maximal NO conversion of c.a. 94% could be achieved at c.a. 275 degrees C at a high GHSV of 180,000 h(-1). For ruthenium catalysts, the effects of supports, ruthenium loadings, pretreatment conditions and experiment conditions (feed gas composition, GHSV) on NO oxidation to NO(2) were investigated in detail. The ruthenium catalysts were characterized by means of X-ray diffraction (XRD), CO pulse chemisorption, transmission electron microscopy (TEM) and temperature-programmed reduction (TPR) techniques. The active ruthenium species for NO oxidation were discussed based on the catalytic and characterization results. Moreover, the reaction mechanism for NO oxidation over Ru/TiO(2) catalyst was studied by means of in situ diffuse reflectance Fourier transform infrared spectroscopy (DRIFTS). (C) 2008 Elsevier B.V. All rights reserved.
机译:通过浸渍法在旋转蒸发仪中制备了一系列TiO(2)负载的催化剂,并评估了NO氧化为NO(2)的能力。在所有研究的催化剂中,Ru / TiO(2)催化剂表现出最佳的活性和c.a的最大NO转化率。大约94%可以达到在GHSV为180,000 h(-1)的情况下为275摄氏度。对于钌催化剂,详细研究了载体,钌负载量,预处理条件和实验条件(进料气组成,GHSV)对NO氧化为NO(2)的影响。通过X射线衍射(XRD),CO脉冲化学吸附,透射电子显微镜(TEM)和程序升温还原(TPR)技术对钌催化剂进行了表征。根据催化和表征结果,讨论了用于氧化NO的活性钌。此外,通过原位漫反射傅里叶变换红外光谱(DRIFTS)研究了Ru / TiO(2)催化剂上NO氧化的反应机理。 (C)2008 Elsevier B.V.保留所有权利。

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