Mahmoudabadi Zohal Safaei, Rashidi Alimorad, Tavasoli Ahmad, Esrafili Mehdi, Panahi Mohammad, Askarieh Mojtaba, Khodabakhshi Saeed
School of Chemistry, College of Science, University of Tehran, Tehran, Iran.
Nanotechnology Research Center, Research Institute of Petroleum Industry, Tehran, Iran.
Ultrason Sonochem. 2021 Jun;74:105558. doi: 10.1016/j.ultsonch.2021.105558. Epub 2021 Apr 22.
In this study, a novel, simple, high yield, and scalable method is proposed to synthesize highly porous MoS/graphene oxide (M-GO) nanocomposites by reacting the GO and co-exfoliation of bulky MoS in the presence of polyvinyl pyrrolidone (PVP) under different condition of ultrasonication. Also, the effect of ultrasonic output power on the particle size distribution of metal cluster on the surface of nanocatalysts is studied. It is found that the use of the ultrasonication method can reduce the particle size and increase the specific surface area of M-GO nanocomposite catalysts which leads to HDS activity is increased. These nanocomposite catalysts are characterized by XRD, Raman spectroscopy, SEM, STEM, HR-TEM, AFM, XPS, ICP, BET surface, TPR and TPD techniques. The effects of physicochemical properties of the M-GO nanocomposites on the hydrodesulfurization (HDS) reactions of vacuum gas oil (VGO) has been also studied. Catalytic activities of MoS-GO nanocomposite are investigated by different operating conditions. M9-GO nanocatalyst with high surface area (324 m/g) and large pore size (110.3 Å), have the best catalytic performance (99.95%) compared with Co-Mo/γAlO (97.91%). Density functional theory (DFT) calculations were also used to elucidate the HDS mechanism over the M-GO catalyst. It is found that the GO substrate can stabilize MoS layers through weak van der Waals interactions between carbon atoms of the GO and S atoms of MoS. At both Mo- and S-edges, the direct desulfurization (DDS) is found as the main reaction pathway for the hydrodesulfurization of DBT molecules.
在本研究中,提出了一种新颖、简单、高产且可扩展的方法,即在聚乙烯吡咯烷酮(PVP)存在下,于不同超声条件下使氧化石墨烯(GO)与块状二硫化钼(MoS)共剥离,以合成高度多孔的二硫化钼/氧化石墨烯(M-GO)纳米复合材料。此外,研究了超声输出功率对纳米催化剂表面金属簇粒径分布的影响。结果发现,使用超声方法可减小粒径并增加M-GO纳米复合催化剂的比表面积,从而提高加氢脱硫(HDS)活性。这些纳米复合催化剂通过X射线衍射(XRD)、拉曼光谱、扫描电子显微镜(SEM)、扫描透射电子显微镜(STEM)、高分辨率透射电子显微镜(HR-TEM)、原子力显微镜(AFM)、X射线光电子能谱(XPS)、电感耦合等离子体质谱(ICP)、比表面积(BET)、程序升温还原(TPR)和程序升温脱附(TPD)技术进行表征。还研究了M-GO纳米复合材料的物理化学性质对减压瓦斯油(VGO)加氢脱硫(HDS)反应的影响。通过不同操作条件研究了MoS-GO纳米复合材料的催化活性。与Co-Mo/γ-Al₂O₃(97.91%)相比,具有高比表面积(324 m²/g)和大孔径(110.3 Å)的M9-GO纳米催化剂具有最佳催化性能(99.95%)。密度泛函理论(DFT)计算也用于阐明M-GO催化剂上的HDS机理。结果发现,GO基底可通过GO的碳原子与MoS的S原子之间的弱范德华相互作用来稳定MoS层。在Mo和S边缘处,直接脱硫(DDS)被发现是DBT分子加氢脱硫的主要反应途径。