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Boreskov Institute of Catalysis of the Siberian Branch of Russian ...

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PP-III-37performed under atmospheric pressure with a quartz-made tubular reactor. The effluents from<strong>the</strong> reactor, containing reaction products were analyzed by gas chromatography.Results and Discussion: The X-ray diffraction peaks <strong>of</strong> Ce 1–x Pr x O 2 samples correspondto <strong>the</strong> face-centered cubic fluorite structure type CeO 2 and PrO 2 . A very homogeneousmaterials with spherical morphology and an insignificantly variation <strong>of</strong> lattice parameter wereevidenced by XRD and SEM microscopy <strong>of</strong> <strong>the</strong> WCe 1–x Pr x O 2 samples with various Prcontent. This may be due to <strong>the</strong> uniformity <strong>of</strong> Pr 4+ : Pr 3+ ratio and oxygen vacancy in <strong>the</strong>sematerials. The lattice parameter systematically increases with <strong>the</strong> Pr content for ECe 1–x Pr x O 2samples and formation <strong>of</strong> two phases was evidenced by SEM microscopy at high Pr percent.The oxidation states <strong>of</strong> cerium and praseodymium ions have been determined by XP and UV-Vis spectroscopy. While cerium is mainly in <strong>the</strong> +4 oxidation state, about one-half <strong>of</strong> <strong>the</strong>praseodymium ions were found to be in <strong>the</strong> +3 state. The large amount <strong>of</strong> Pr 3+ cations seemsto be a particularity <strong>of</strong> <strong>the</strong> doped ceria samples.A high variation <strong>of</strong> <strong>the</strong> surface stoichiometry and Pr 4+ : Pr 3+ ratio was evidenced for <strong>the</strong> Wand E type samples. The catalytic performance <strong>of</strong> oxides depends strongly on <strong>the</strong> precipitateC CH4, %10080604020Ce0,9Pr0,1O2(W)Ce0,1Pr0,9O2(W)Ce0,5Pr0,5O2(W)Ce0,9Pr0,1O2(E)Ce0,5Pr0,5O2(E)washing. The catalytic activity is probablyattributable to <strong>the</strong> migration <strong>of</strong> Pr ions and<strong>the</strong>ir distribution at interface or into <strong>the</strong>ceria network. The activity <strong>of</strong> allWCe 1–x Pr x O 2 samples in oxidation <strong>of</strong> CH 4is very high (Fig. 1). In contrast,ECe 1–x Pr x O 2 samples exhibit lower0370 420 470 520Temperature, o Cactivity. The activity <strong>of</strong> ECe 1–x Pr x O 2increases with Pr content.Fig. 1. The variation <strong>of</strong> CH 4 conversion with temperature.Acknowledgements: The financial support by <strong>the</strong> Romanian Ministry <strong>of</strong> Education andResearch -CEEX-AMCSIT 267 is highly appreciated.References1. A. Hartridge, M. Ghanashyam Krishna, A.K. Bhattacharya, Mat. Sci. Eng. B57 (1999) 173.2. L. Gerward, J. Staun Olsen, L. Petit, G. Vai<strong>the</strong>eswaran, V. Kanchana, A. Svane, J. Alloys Compounds, 400(2005) 56.3. S. Colussi, C. de Leitenburg, G. Dolcetti, A. Trovarelli, J. Alloys Compounds, 374 (2004) 387.374

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