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Catalytic Oxidation of n-Decane, n-Hexane, and Propane over Pt/CeO2 Catalysts
Xiaohui Gao1, Yuting Bai1, Hao Zhang1
1Research Institute of Industrial Catalysis, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, PR China.
Abstract:
Pt species with different chemical states and structures were supported on CeO2 by solution reduction (Pt/CeO2-SR) and wet impregnation (Pt/CeO2-WI) and investigated in catalytic oxidation of n-decane (C10H22), n-hexane (C6H14), and propane (C3H8). Characterization by X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, H2-temperature programming reduction, and oxygen temperature-programmed desorption showed that Pt0 and Pt2+ existed on Pt nanoparticles of the Pt/CeO2-SR sample, which promoted redox, oxygen adsorption, and activation. On Pt/CeO2-WI, Pt species were highly dispersed on CeO2 as the Pt-O-Ce structure, in which surface oxygen decreased significantly. The Pt/CeO2-SR catalyst presents high activity in oxidation of C10H22 with a rate of 0.164 μmol min-1 m-2 at 150 °C. The rate increased with oxygen concentration. Moreover, Pt/CeO2-SR presents high stability on feed stream containing 1000 ppm C10H22 at gas hour space velocity = 30,000 h-1 as low as 150 °C for 1800 min. The low activity and stability of Pt/CeO2-WI were probably related to its low availability of surface oxygen. In situ Fourier transform infrared results showed that the adsorption of alkane occurred through the interaction with Ce-OH. The adsorption of C6H14 and C3H8 was much weaker than that of C10H22, which resulted in the decrease in activity for C6H14 and C3H8 oxidation of Pt/CeO2 catalysts.
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