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Methanation of CO2 with H2-reduced magnetite
Authors:Takashi Yoshida  Kenichi Nishizawa  Masahiro Tabata  Hiroshi Abe  Tatsuya Kodama  Masamichi Tsuji  Yutaka Tamaura
Affiliation:(1) Department of Chemistry, Research Center for Carbon Recycling and Utilization, Tokyo Institute of Technology, Ookayama, Meguro-ku, Tokyo 152, Japan
Abstract:The methanation reaction of CO2 was studied with H2-reduced magnetite. A high conversion ratio of about 0.9 (in 30 min of the reaction time) with a selectivity of nearly 100% was obtained at 300°C and at 0.1 MPa for H2-reduced magnetite which had been prepared by passing H2 gas for 1–5 h at 300°C. From the results of X-ray diffractometry and Mössbauer spectroscopy, and from chemical analysis of the deposited carbon, H2-reduced magnetite is considered to decompose adsorbed CO2 into carbon, and to incorporate the oxygen of the CO2 into the spinel-type structure of the magnetite, associated with oxidation of the Fe2+ ion into Fe3+ ion in the magnetite. The high conversion ratio in the methanation reaction is considered to come from a higher reactivity of the elementary carbon deposited on the surface of the H2-reduced magnetite.
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