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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:镍基催化剂上甲烷化和脱硫原位反应活性位的研究

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Supported nickel oxide based catalysts of Fe/ Co/ Ni (10: 30: 60)-Al 2 O 3 and Pr/ Co/ Ni (5: 35: 60)-Al 2 O 3 that were prepared by wetness impregnation method showed potential catalysts for the in-situ reactions of H 2 S desulfurization and CO 2 methanation from ambient temperature up to 300 o C. ? X-ray Photoelectron Spectroscopy revealed Ni 2 O 3 and Fe 3 O 4 as the surface active components on the Fe/ Co/ Ni (10: 30: 60)-Al 2 O 3 catalyst, while Ni 2 O 3 and Co 3 O 4 on the Pr/ Co/ Ni (5: 35: 60)-Al 2 O 3 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)-Al 2 O 3 and Pr/ Co/ Ni (5: 35: 60)-Al 2 O 3 catalysts, respectively. ? N 2 adsorption-desorption analysis showed reduction of 5.5 % on the surface area of the spent Fe/ Co/ Ni (10: 30: 60)-Al 2 O 3 catalyst. However, the surface area of the spent Pr/ Co/ Ni (5: 35: 60)-Al 2 O 3 catalyst increased by 8.6 %.
机译:通过湿式浸渍法制备的负载型Fe / Co / Ni(10:30:60)-Al 2 O 3和Pr / Co / Ni(5:35:60)-Al 2 O 3的氧化镍基催化剂显示出潜力H 2 S脱硫和CO 2甲烷化从环境温度到300 o C的原位反应的催化剂。 X射线光电子能谱表明,Ni 2 O 3和Fe 3 O 4是Fe / Co / Ni(10:30:60)-Al 2 O 3催化剂上的表面活性成分,而Ni 2 O 3和Co 3 O 4在Pr / Co / Ni(5:35:60)-Al 2 O 3催化剂上。 ?能量色散X射线分析表明,废Fe / Co / Ni(10:30:60)-Al 2 O 3和Pr / Co / Ni(5:35:60)中存在2.7%和0.9%的硫-Al 2 O 3催化剂分别。 ? N 2吸附-解吸分析表明,废Fe / Co / Ni(10:30:60)-Al 2 O 3催化剂的表面积减少了5.5%。但是,用过的Pr / Co / Ni(5:35:60)-Al 2 O 3催化剂的表面积增加了8.6%。

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