Surface properties of Ru®particles supported on carbon materials: A microcalorimetric study of the effects over the CO chemisorptions of residual anionic species

被引:12
作者
Guerrero-Ruiz, A. [1 ,2 ]
Gallegos-Suarez, E. [1 ,3 ]
Gonzalo-Chacon, L. [3 ]
Rodriguez-Ramos, I. [3 ]
机构
[1] UNED, Dept Quim Inorgan & Tecn, Fac Ciencias, Madrid 28040, Spain
[2] Unidad Asociada UNED CSIC ICP, Grp Diseno & Aplicac Catalizadores Heterogeneos, Madrid, Spain
[3] CSIC, Inst Catalisis & Petroleoquim, E-28049 Madrid, Spain
关键词
Supported metal catalysts; Carbon supports; CO adsorption; Microcalorimetry; METALLIC CLUSTERS; ADSORPTION; CATALYSTS; HYDROGEN; RU;
D O I
10.1016/j.tca.2012.11.019
中图分类号
O414.1 [热力学];
学科分类号
摘要
Chemisorption of CO combined with microcalorimetry has been applied to study the nature, number and adsorption strength distribution of surface sites exposed by carbon-supported Ru catalysts. A comparative analysis of the CO chemisorption on different Ru catalysts, prepared using two different metal precursors, RuCl3 center dot xH(2)O and Ru(NO)(NO3)(3), has been carried out. An activated carbon and the corresponding derivative where oxygen surface groups were incorporated, as well as carbon nanotubes and a high surface area graphite, were used as catalytic supports. Based on previous temperature programmed reduction studies, all the catalysts were reduced under hydrogen flow at 523 K or at 573 K. The CO adsorption differential enthalpy profiles show that Ru(NO)(NO3)(3) precursor produces more homogeneous surface site distribution in the Ru nanocrystals, in comparison with those prepared from RuCl3, as well as higher values of enthalpies in the medium range of coverage. As a possible explanation for this effect, residual chloride species remaining after reduction treatment in the ex-chloride catalysts, that can be anchored to the Ru nanoparticles weakening the CO adsorption, have been considered. This behavior occurs for the three studied carbon supports. On the other hand, the oxygen surface groups incorporated on the activated carbon seem not to modify the CO adsorption properties of the catalysts, independently of the precursor employed. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:112 / 117
页数:6
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