Chen Guoliang, Xie Wenpeng, Li Qinghong, Wang Wentai, Bing Liancheng, Wang Fang, Wang Guangjian, Fan Chunyan, Liu Shaomin, Han Dezhi
State Key Laboratory Base of Eco-chemical Engineering, College of Chemical Engineering, Qingdao University of Science and Technology Qingdao 266042 China
WA School of Mines: Minerals, Energy and Chemical Engineering, Curtin University GPO Box U1987 Perth WA 6845 Australia.
RSC Adv. 2020 Oct 8;10(61):37280-37286. doi: 10.1039/d0ra07153f. eCollection 2020 Oct 7.
The introduction of surfactants during the fabrication of hydrodesulfurization catalysts could not only tune the microstructure but also promote the dispersion of active components. In this work, CoMo bulk catalysts with the hierarchical structure of three-dimensionally ordered macro-mesopores were successfully fabricated by using a colloidal crystal template with the addition of PEG 400 and/or F127 surfactants. The obtained samples were characterized by various techniques, and the possible mechanism of the structure formation was also discussed. The characterization and evaluation results reveal that the addition of surfactants can promote the formation of the mesopores (3-4 nm) inside the macroporous walls of these bulk catalysts, which is essential for the increase of catalyst surface area, and the active sites for reaction. The CoMo-PF-1 catalyst displayed superior catalytic performance for thiophene hydrodesulfurization with the thiophene conversion of 99.4% under 1 MPa at 360 °C, which is much higher than that (77.8%) at 0.1 MPa. This result is even comparable to our previous report with the thiophene conversion of 99.2% over the 3DOM CoMo catalyst under 3 MPa.
在加氢脱硫催化剂制备过程中引入表面活性剂,不仅可以调节微观结构,还能促进活性组分的分散。在本工作中,通过使用胶体晶体模板并添加聚乙二醇400和/或F127表面活性剂,成功制备了具有三维有序大孔-介孔分级结构的CoMo整体催化剂。采用多种技术对所得样品进行了表征,并探讨了结构形成的可能机理。表征和评价结果表明,表面活性剂的添加能够促进这些整体催化剂大孔壁内部介孔(3-4纳米)的形成,这对于增加催化剂表面积和反应活性位点至关重要。CoMo-PF-1催化剂在360℃、1MPa条件下对噻吩加氢脱硫表现出优异的催化性能,噻吩转化率达99.4%,远高于0.1MPa时的转化率(77.8%)。该结果甚至与我们之前的报道相当,即在3MPa下,3DOM CoMo催化剂上噻吩转化率为99.2%。