Hubei Key Laboratory of Coal Conversion and New Carbon Material, School of Chemical Engineering and Technology, Wuhan University of Science and Technology, Wuhan 430081, China.
Key Laboratory of Catalysis and Materials Science of the State Ethnic Affairs Commission & Ministry of Education, South-Central University for Nationalities, Wuhan 430074, China.
Nanoscale. 2017 Jan 5;9(2):570-581. doi: 10.1039/c6nr07529k.
A series of nanofibrous alumina materials with diameters of 4-6 nm and with different aspect ratios ranging from 3 to 16 were prepared. Cobalt impregnated catalysts were prepared by means of incipient wetness impregnation on alumina nanofibers while the 'rearranged' catalysts were prepared by using ultrasonication assistance to mix the fibers with the CoO nanoparticles. The effects of the alumina nanofiber aspect ratios on the Co catalyst structure and performance for Fischer-Tropsch synthesis were studied. The pore size of the two series of catalysts increased as the aspect ratio of the alumina nanofiber increased. For impregnated catalysts, large CoO particles were formed on the external surface of the alumina support when the aspect ratio was 3 and 5, while the crystallite sizes of CoO increased from 13.3 nm to 15.6 nm with the increase of the aspect ratio from 7 to 16. The four 'rearranged' catalysts possessed similar and homogeneously dispersed CoO crystallites of 9.5 nm. As expected the reduction behavior of the two series of catalysts was primarily influenced by the CoO crystallite size and structure. The FT data of the two series of catalysts indicate that dispersed Co catalysts on alumina nanofibers with large aspect ratios having large inter-crystallite pores significantly improve the catalyst activity and C selectivity. The FT data of the 'rearranged' catalysts strongly demonstrated that the internal mass transfer of reactants and products increased with a decrease in inter-crystallite pore size, resulting in a decrease of C selectivity and C olefin/paraffin ratio, and an increase of CH selectively, while the CO consumption rate was little altered. Furthermore, catalytic stability tests showed that the alumina nanofibers with larger aspect ratios inhibited Co migration and coalescence in the matrices of the nanofibrous alumina, and this significantly enhanced the stability of the catalyst. The Co/AlO-16 catalyst possessing uniformly distributed cobalt, improved reducibility and large pores is the preferred choice to generate high catalytic activity, stability and C selectivity.
一系列直径为 4-6nm 且具有不同纵横比(3-16)的纳米纤维氧化铝材料被制备。通过在氧化铝纳米纤维上进行初始湿浸渍制备钴浸渍催化剂,而“重排”催化剂则通过使用超声处理来混合纤维与 CoO 纳米颗粒来制备。研究了氧化铝纳米纤维纵横比对费托合成用 Co 催化剂结构和性能的影响。随着氧化铝纳米纤维纵横比的增加,两系列催化剂的孔径均增大。对于浸渍催化剂,当纵横比为 3 和 5 时,大的 CoO 颗粒在氧化铝载体的外表面形成,而 CoO 的晶粒尺寸从 13.3nm 增加到 15.6nm,随着纵横比从 7 增加到 16。四个“重排”催化剂具有相似且均匀分散的 9.5nm CoO 结晶。正如预期的那样,两系列催化剂的还原行为主要受 CoO 结晶度和结构的影响。两系列催化剂的 FT 数据表明,在具有大纵横比的氧化铝纳米纤维上分散的 Co 催化剂具有大的晶间孔,显著提高了催化剂的活性和 C 选择性。“重排”催化剂的 FT 数据强烈表明,随着晶间孔径的减小,反应物和产物的内部传质增加,导致 C 选择性和 C 烯烃/烷烃比降低,CH 选择性增加,而 CO 消耗速率几乎没有变化。此外,催化稳定性测试表明,具有较大纵横比的氧化铝纳米纤维抑制了 Co 在纳米纤维氧化铝基质中的迁移和聚集,这显著提高了催化剂的稳定性。具有均匀分布钴、改善的还原性和大孔的 Co/AlO-16 催化剂是产生高催化活性、稳定性和 C 选择性的首选。