Key Laboratory of Applied Chemistry of Zhejiang Province, Department of Chemistry, Zhejiang University, Hangzhou 310028 PR China.
ChemSusChem. 2012 Apr;5(4):727-33. doi: 10.1002/cssc.201100476. Epub 2012 Feb 28.
Ordered mesoporous carbon (OMC)-supported molybdenum carbide catalysts were successfully prepared in one pot using a solvent-evaporation-induced self-assembly strategy accompanied by a carbothermal hydrogen reduction reaction. Characterization with nitrogen sorption, small-angle XRD, and TEM confirmed that the obtained materials had high surface areas, large pore volumes, ordered mesoporous structures, narrow pore size distributions, and uniform dispersions of molybdenum carbide particles. With nitrogen replaced by hydrogen in the carbothermal reduction reaction, the formation temperature of molybdenum carbide could be reduced by more than 100 °C. By changing the amount of molybdenum precursor added from less than 2 % to more than 5 %, molybdenum carbide structures could be easily regulated from Mo(2) C to MoC. The catalytic performance of OMC-supported molybdenum carbide catalysts was evaluated by hydrodeoxygenation of vegetable oils. Compared with Mo(2)C, MoC exhibited high product selectivity and excellent resistance to leaching in the conversion of vegetable oils into diesel-like hydrocarbons.
有序介孔碳(OMC)负载碳化钼催化剂采用溶剂挥发诱导自组装策略,伴随碳热氢还原反应,一锅法成功制备。氮气吸附、小角 XRD 和 TEM 表征证实,所获得的材料具有高比表面积、大孔体积、有序介孔结构、窄孔径分布和碳化钼颗粒的均匀分散。在碳热还原反应中用氢取代氮,可以将碳化钼的形成温度降低 100°C 以上。通过改变加入的钼前驱体的量(从小于 2%到大于 5%),可以很容易地将碳化钼结构从 Mo2C 调节到 MoC。通过加氢脱氧评价 OMC 负载碳化钼催化剂在植物油转化为柴油类烃中的催化性能。与 Mo2C 相比,MoC 在植物油转化为柴油类烃的过程中表现出较高的产物选择性和优异的抗浸出性。