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以未硅烷化和硅烷化的SBA-15为载体,采用满孔浸渍法制备了钴基费-托合成催化剂,通过元素分析、N_2吸附-脱附、X射线衍射、H_2程序升温还原、H_2程序升温脱附以及氧滴定等手段对催化剂进行了表征.催化剂的费-托合成活性测试在固定床反应器上进行.研究表明,对于SBA-15硅烷化后制备的催化剂,金属钴与载体之间的相互作用降低,氧化钴的还原度增加.随着三甲基氯硅烷用量的增加,三甲基硅基的表面覆盖度增加,钴的晶粒直径增大.硅烷化后的催化剂的高活性归因于高的还原度.而C_(5+)选择性的增加则归因于钴晶粒直径的增大.

Cobalt catalysts supported on unsilylated and silylated SBA-1S were prepared by incipient wetness impregnation and characterized by elemental analysis, N_2 adsorption-desorption, X-ray diffraction, H_2 temperature-programmed reduction, H_2 temperature-programmed desorption, and oxygen titration. Their catalytic properties for Fischer-Tropsch synthesis were evaluated in a fixed-bed reactor. The results show that the interaction between cobalt and the support was decreased, and the reducibility of the cobalt oxide species was more facile on the silylated Co/SBA-15 catalyst. With increasing (CH_3)_3SiCl loading, the surface coverage of the trimethylsilyl group increased, and the cobalt cluster size was larger. The higher activity of the silylated 10%Co/SBA-15 catalysts was ascribed to its improved reducibility. The increase in selectivity for C_(5+) hydrocarbons was attributed to the increase in cobalt cluster size.

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