Oxidation of lean methane over cobalt catalysts supported on ceria/alumina

催化作用 尖晶石 物理吸附 材料科学 无机化学 氧化钴 甲烷 拉曼光谱 X射线光电子能谱 氢溢流 化学工程 化学 冶金 有机化学 工程类 物理 光学 生物化学
作者
Andoni Choya,Beatriz de Rivas,Juan R. González‐Velasco,Jose Ignacio Gutiérrez-Ortiz,Rubén López‐Fonseca
出处
期刊:Applied Catalysis A-general [Elsevier]
卷期号:591: 117381-117381 被引量:33
标识
DOI:10.1016/j.apcata.2019.117381
摘要

Cobalt (30 %wt.) oxide catalysts supported over ceria-modified (3–18 %wt.) alumina supports were examined for the combustion of lean methane. The prepared samples were characterised by wavelength dispersive X-ray fluorescence, N2 physisorption, X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, temperature-programmed reduction with hydrogen and temperature-programmed reaction with methane. A significant enhancement of the activity was evidenced with respect to the catalyst supported over bare alumina, with an optimal cerium loading of 12 %wt. and a resultant T50 value of 480 °C. The ceria modification was found to induce a dual positive effect on the performance of the cobalt catalysts. On one hand, it acted as a physical barrier between deposited cobalt and alumina, thus inhibiting the cobalt-alumina interaction and the subsequent cobalt aluminate formation. On the other hand, the insertion of cerium ions in the spinel lattice led to a distortion of the structure that in turn resulted in an enhanced mobility of the oxygen species. The optimised catalyst exhibited a relatively good thermal stability for prolonged reaction time intervals (150 h) under dry conditions. The presence of water vapour markedly affected the catalytic performance although this negative effect was partially reversible.

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