以介孔分子筛SBA-15为载体,乙酸钴为钴源,采用浸渍法制备了2wt％、4wt％、8wt％、10wt％和20wt％Co负载量的Co/SBA-15介孔材料.采用FT-IR、XRD、N2物理吸附、UV-Vis、SEM、TEM、H2-TPR等技术对催化材料的结构进行表征,并将其应用于环己基过氧化氢分解反应.结果表明:负载金属钴后,载体的介孔结构保持完好,随着负载量的增加,Co/SBA-15的比表面积、总孔体积和平均孔径不断减小,Co由骨架内均匀分散状态向氧化物Co3O4的形式转变.不同负载量的Co/SBA-15在环己基过氧化氢分解反应中均表现出较好的催化性能,其中8wt％Co/SBA-15催化环己基过氧化氢的转化率达到98.1％,环己醇和环己酮的选择性分别为70.9％和27.9％.当负载量相对较低时,钴的流失使催化性能下降明显,只有当钴负载量增加到20wt％,主要以Co3O4形式存在时,钴的流失速率得到抑制,连续使用五次后仍能保持较高的活性和选择性.
A series of mesoporous material Co/SBA-15 with Co loading of 2wt％,4wt％,8wt％,10wt％,and 20wt％ were prepared through incipient wetness impregnation method using SBA-15 as support and cobalt acetate as Co source.The structures of obtained samples were characterized by FT-IR,X-ray diffraction (XRD),N2 adsorption-desorption,Diffuse reflectance UV-Vis,SEM,TEM,and hydrogen temperature programmed reduction (H2-TPR) techniques.Their catalytic performance in decomposition of cyclohexyl hydroperoxide were also studied.Results show that the mesoporous structure of support remains intact after loading with Co.The specific surface area,pore volume and pore diameter of Co/SBA-15 are gradually decreased with the increase of loading amount.All the samples showed excellent catalytic activity in the decomposition of cyclohexyl hydroperoxide.The 8％Co/SBA-15 showed the highest catalytic performance with a conversion of 98.1％ and selectivity of cyclohexanone 70.9％ and cyclohexanol 27.9％.However,the loss of Co from the lower loading amount samples resulted in catalytic performance decreased significantly after reuse.Only when the loading of Co increases to 20％ mainly in the form of Co3O4,the loss rate of Co can be inhibited and the catalytic activity and selectivity of recovered catalyst remain constant after using for five times.
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