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Combustion Synthesis of Non-Precious CuO-CeO₂ Nanocrystalline Catalysts with Enhanced Catalytic Activity for Methane
Abdallah F Zedan1, Amina S AlJaber2
1Department of Laser Applications in Metrology, Photochemistry and Agric., National Institute of Laser Enhanced Sciences, Cairo University, Giza 12613, Egypt. azedan@niles.edu.eg.
Abstract:
In this study, xCuO-CeO₂ mixed oxide catalysts (Cu weight ratio x = 1.5, 3, 4.5, 6 and 15 wt.%) were prepared using solution combustion synthesis (SCS) and their catalytic activities towards the methane (CH₄) oxidation reaction were studied. The combustion synthesis of the pure CeO₂ and the CuO-CeO₂ solid solution catalysts was performed using copper and/or cerium nitrate salt as an oxidizer and citric acid as a fuel. A variety of standard techniques, including scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), thermo-gravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy were employed to reveal the microstructural, crystal, thermal and electronic properties that may affect the performance of CH₄ oxidation. The CuO subphase was detected in the prepared solid solution and confirmed with XRD and Raman spectroscopy, as indicated by the XRD peaks at diffraction angles of 35.3° and 38.5° and the Ag Raman mode at 289 cm-1, which are characteristics of tenorite CuO. A profound influence of Cu content was evident, not only affecting the structural and electronic properties of the catalysts, but also the performance of catalysts in the CH₄ oxidation. The presence of Cu in the CeO₂ lattice obviously promoted its catalytic activity for CH₄ catalytic oxidation. Among the prepared catalysts, the 6% CuO-CeO₂ catalyst demonstrated the highest performance, with T50 = 502 °C and T80 = 556 °C, an activity that is associated with the availability of a fine porous structure and the enhanced surface area of this catalyst. The results demonstrate that nanocrystalline copper-ceria mixed oxide catalysts could serve as an inexpensive and active material for CH₄ combustion.
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