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The investigation of active sites on nickel oxide based catalysts towards the in-situ reactions of methanation and desulfurization

机译:氧化镍基催化剂上甲烷化和脱硫原位反应的活性位研究

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摘要

Supported nickel oxide based catalysts of Fe/ Co/ Ni (10: 30: 60)-Al2O3 and Pr/ Co/ Ni (5: 35: 60)-Al2O3 that were prepared by wetness impregnation method showed potential catalysts for the in-situ reactions of H2S desulfurization and CO2 methanation from ambient temperature up to 300 oC. X-ray Photoelectron Spectroscopy revealed Ni2O3 and Fe3O4 as the surface active components on the Fe/ Co/ Ni (10: 30: 60)-Al2O3 catalyst, while Ni2O3 and Co3O4 on the Pr/ Co/ Ni (5: 35: 60)-Al2O3 catalyst. Energy Dispersive X-ray analysis indicated the presence of 2.7 % and 0.9 % of sulfur on the spent Fe/ Co/ Ni (10: 30: 60)-Al2O3 and Pr/ Co/ Ni (5: 35: 60)-Al2O3 catalysts, respectively. N2 adsorption-desorption analysis showed reduction of 5.5 % on the surface area of the spent Fe/ Co/ Ni (10: 30: 60)-Al2O3 catalyst. However, the surface area of the spent Pr/ Co/ Ni (5: 35: 60)-Al2O3 catalyst increased by 8.6 %.
机译:Fe / Co / Ni(10:30:60)-Al2O3和Pr / Co / Ni(5:35:60)-Al2O3的负载型氧化镍基催化剂显示了潜在的原位催化剂H2S脱硫和CO2甲烷化在环境温度高达300 oC时的反应。 X射线光电子能谱显示,Ni2O3和Fe3O4是Fe / Co / Ni(10:30:60)-Al2O3催化剂上的表面活性成分,而Ni2O3和Co3O4在Pr / Co / Ni(5:35:60)上-Al2O3催化剂。能量色散X射线分析表明,废Fe / Co / Ni(10:30:60)-Al2O3和Pr / Co / Ni(5:35:60)-Al2O3催化剂上存在2.7%和0.9%的硫, 分别。 N 2吸附-解吸分析表明,废Fe / Co / Ni(10:30:60)-Al2O3催化剂的表面积减少了5.5%。但是,用过的Pr / Co / Ni(5:35:60)-Al2O3催化剂的表面积增加了8.6%。

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