K. Hadjiivanov, M. Mihaylov, N. Abadjieva, D. Klissurski
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引用次数: 26
摘要
通过浸渍(Ni-i- ti样品)、碱性介质中Ni2+离子在TiO2 (Ni-1- ti样品)和还原Ni-1- ti (Ni-2- ti样品)上吸附制备了3种Ni/TiO2样品。用TPR、吸附CO的红外光谱和x射线衍射对样品进行了表征。与吸附技术相比,浸渍导致活性相分布不均匀,还原温度可忽略不计。Ni-i-Ti的还原形成了平均直径为22 nm的镍颗粒。用CO法测定表面氮。还原后的Ni-1-Ti样品中镍颗粒的平均直径约为20 nm。然而,在这种情况下,表面没有检测到金属镍,即金属颗粒被封装在支架中。在Ni-1-Ti中镍的还原过程中,大部分吸附活性位点得以再生,使得Ni2+离子再次吸附在样品上。结果,镍的浓度增加。还原后的Ni-2-Ti上镍颗粒的平均直径保持在20 nm左右,与还原后的Ni-1-Ti样品相似。而Ni-2-Ti则通过CO吸附法检测表面金属镍。结果表明,通过Ni2+离子的连续吸附还原,可以制备出具有理想镍浓度的二氧化钛负载型镍催化剂,并使金属颗粒不被包裹在载体中。本文还讨论了强金属-支撑相互作用(SMSI)机理的一些新方面。
Characterization of Ni/TiO2 catalysts prepared by successive adsorption–reduction of Ni2+ ions
Three Ni/TiO2 samples have been synthesized by impregnation (sample Ni-i-Ti), adsorption of Ni2+ ions from alkaline media on TiO2 (sample Ni-1-Ti) and on reduced Ni-1-Ti (sample Ni-2-Ti). The samples have been characterized by TPR, IR spectroscopy of adsorbed CO and X-ray diffraction. Impregnation leads to a less homogeneous distribution of the active phase and a negligibly lower temperature of reduction as compared with the adsorption technique. Reduction of Ni-i-Ti results in the formation of nickel particles with an average diameter of 22 nm. Surface N was detected by CO testing. The average diameter of the nickel particles in the reduced Ni-1-Ti sample is about 20 nm. In this case, however, no metal nickel was detected on the surface, i.e. the metal particles are encapsulated in the support. The majority of the active sites for adsorption are regenerated during the reduction of nickel in Ni-1-Ti, which allows Ni2+ ions to be adsorbed again on the sample. As a result, the nickel concentration increases. The mean diameter of the nickel particles on reduced Ni-2-Ti remains of the order of 20 nm, similar to the case of the reduced Ni-1-Ti sample. With Ni-2-Ti, however, surface metal nickel was detected by CO adsorption. It is concluded that successive absorption–reduction of Ni2+ ions might be used to prepare titania supported nickel catalyst with a desired nickel concentration and metal particles that are not encapsulated in the support. Some new aspects of the strong metal–support interaction (SMSI) mechanism are also discussed.