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Study on chemisorption of H2, O2, CO and C2H4on Pt-Ag/SiO2catalysts by microcalorimetry and FTIR
Authors:L. Li  X. Wang  J. Shen  L. Zhou  T. Zhang
Affiliation:1.State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences;2.State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences;3.Department of Chemistry, Nanjing University;4.State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences;5.State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences
Abstract:
Adsorption microcalorimetry has been employed to study the interaction of ethylene with the reduced and oxidized Pt-Ag/SiO2catalysts with different Ag contents to elucidate the modified effect of Ag towards the hydrocarbon processing on platinum catalysts. In addition, microcalorimetric adsorption of H2, O2, CO and FTIR of CO adsorption were conducted to investigate the influence of Ag on the surface structure of Pt catalyst. It is found from the microcalorimetric results of H2and O2adsorption that the addition of Ag to Pt/SiO2leads to the enrichment of Ag on the catalyst surface which decreases the size of Pt surface ensembles of Pt-Ag/SiO2catalysts. The microcalorimetry and FTIR of CO adsorption indicates that there still exist sites for linear and bridged CO adsorption on the surface of platinum catalysts simultaneously although Ag was incorporated into Pt/SiO2. The ethylene microcalorimetric results show that the decrease of ensemble size of Pt surface sites suppresses the formation of dissociative species (ethylidyne) upon the chemisorption of C2H4on Pt-Ag/SiO2. The differential heat vs. uptake plots for C2H4adsorption on the oxygen-preadsorbed Pt/SiO2and Pt-Ag/SiO2catalysts suggest that the incorporation of Ag to Pt/SiO2could decrease the ability for the oxidation of C2H4.
Keywords:
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