甲烷化
钼
化学
催化作用
碳化物
氮化物
硫化物
镍
无机化学
金属
加氢脱硫
二硫化钼
硫化镍
冶金
有机化学
材料科学
图层(电子)
标识
DOI:10.1016/0021-9517(81)90289-x
摘要
Several molybdenum compounds-oxides, sulfide, metal, carbide, and nitride—were prepared, and their catalytic properties in the hydrogenation of CO2 at 350 °C were investigated and compared with those of nickel and iron. The initial specific activities, rates per unit surface area of catalyst, decreased in the sequence Ni > Mo carbide > Mo metal > Mo nitride > MoO2 > MoS2 > MoO3. Iron deactivated so rapidly that its initial activity could not be determined. The molybdenum compounds produced very much smaller amounts of C2 and C3 hydrocarbons in the hydrogenation of CO2 than in that of CO. Iron produced the largest amount of higher hydrocarbons from CO2, and Ni only CH4. The molybdenum compounds, except MoS2 and MoO3, had high activities for watergas-shift reaction.
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