E. V. Matus, E. N. Kovalenko, O. B. Sukhova, S. A. Yashnik, I. Z. Ismagilov, M. A. Kerzhentsev, S. R. Khairulin
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引用次数: 0
Abstract
Efficient production of H2 by combined (steam/CO2; steam/O2) reforming of CH4 was comparatively studied over perovskite-derived promoted Ni catalysts. The process performance was improved by regulating the redox and structural properties of the LaNi0.99M0.01O3 catalysts through promotion (M = Pt, Pd, Re, Mo, Sn). The catalysts were synthesized using the citrate sol–gel method, tested in combined reforming of methane and studied by X-ray fluorescence analysis, thermal analysis, N2 adsorption, X-ray diffraction, electron microscopy, temperature-programed hydrogen reduction to elucidate the impact of catalyst properties on their activity and resistance to re-oxidation and formation of carbon deposits under reaction conditions. It was shown that LaNi0.99M0.01O3 catalysts after calcination at 850 °C in air have a perovskite structure that was destroyed after reductive activation with formation of metal Nio particles with an average size of ~ 25 nm on the surface of lanthanum oxide/hydroxide. The resistance to re-oxidation of Nio particles depends on the type of promoter and is maximum in the case of M = Re. It was established that the type of promoter affects the conversion of reagents (CH4, CO2) and the H2 yield, which at 700 °C increases in the series of promoters Sn < Mo < Pt < Pd < Re in the case of steam/CO2 reforming and Pt < Sn < Mo < Pd < Re with steam/O2 reforming. The optimal composition of catalyst was identified: among the studied samples, LaNi0.99Re0.01O3 is characterized by a higher specific surface area, average reduction ability and high resistance to re-oxidation and coking. At 850 °C it provides the H2 yield of 95 and 50% at complete CH4 conversion in steam/CO2 and steam/O2 reforming, respectively.
期刊介绍:
Catalysis Letters aim is the rapid publication of outstanding and high-impact original research articles in catalysis. The scope of the journal covers a broad range of topics in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis.
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