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The Investigation of Active Sites on Nickel Oxide Based Catalysts towards the In-situ Reactions of Methanation and Desulfurization
Author(s) -
Wan Azelee Wan Abu Bakar,
Mohd. Yusuf Othman,
Rusmidah Ali,
Ching Kuan Yong,
Susilawati Toemen
Publication year - 2009
Publication title -
modern applied science
Language(s) - English
Resource type - Journals
eISSN - 1913-1852
pISSN - 1913-1844
DOI - 10.5539/mas.v3n2p35
Subject(s) - catalysis , methanation , nickel , flue gas desulfurization , x ray photoelectron spectroscopy , incipient wetness impregnation , oxide , materials science , adsorption , inorganic chemistry , desorption , sulfur , nuclear chemistry , chemistry , chemical engineering , metallurgy , organic chemistry , engineering , selectivity

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 %.

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