Citation: Wen-Wu ZHOU, Shi-Yu HAN, Zhi-Ping CHEN, Ying-Feng DUAN, Jie KANG, Fei FAN, Chang TIAN, Xin-Meng ZHANG. Hierarchical TS-1 zeolite loaded with NiMo catalysts: Preparation and performance in hydrodesulfurization[J]. Chinese Journal of Inorganic Chemistry, ;2023, 39(5): 891-905. doi: 10.11862/CJIC.2023.049 shu

Hierarchical TS-1 zeolite loaded with NiMo catalysts: Preparation and performance in hydrodesulfurization

  • Corresponding author: Zhi-Ping CHEN, cupczp@163.com
  • Received Date: 5 December 2022
    Revised Date: 23 March 2023

Figures(9)

  • The sole micropores strictly restrict the wide utilization of TS-1 zeolite in the catalytic fields, especially in the catalytic conversion of compounds with large molecular sizes. Here, we report a feasible and economical method to overcome this drawback. In this work, the hierarchical TS-1 zeolite was constructed via post-acid treatment, postalkali etching, and a combination of postacid treatment and alkali etching methods, after which, the corresponding NiMo-supported catalysts were prepared via the incipient wetness impregnation method. Then, the aforementioned materials were fully characterized using X - ray diffraction (XRD), N2 adsorption - desorption, pyridine adsorbed Fourier transform infrared spectroscopy (Py - FTIR), H2 temperature programmed reduction (H2 - TPR), X-ray photoelectron spectroscopy (XPS), and high-resolution transition electron microscope (HR-TEM) to unravel the changes in the physicochemical properties caused by the post treatments. Finally, the hydrodesulfurization of dibenzothiophene (DBT) was used as a probe to assess the effects of the post-treatments on the catalytic performance of the hierarchical NiMo/TS-1 catalysts. The results showed that the MFI topology of TS-1 zeolite remained undamaged significantly and the serial hierarchical TS-1 zeolites exhibited higher specific surface areas and mesopore structures. Moreover, appropriate amounts of Br?nsted acid sites were formed at the surface of the serial hierarchical TS-1 zeolites. The interaction between the active metals and the support materials was also modulated by the posttreatment of TS-1 zeolite, which resulted in better dispersion of Ni promoted MoS2 slabs with a higher proportion of NiMoS active phase, further leading to the enhanced catalytic activity and direct desulfurization pathway selectivity of the corresponding serial hierarchical NiMo/TS-1 catalysts. Among all the prepared catalysts, the catalytic activity was enhanced by approximately 1.2 times over catalyst NiMo/AT-TS-1 obtained by post-acid treatment compared to that over catalyst NiMo/TS-1 without treatment and on which the selectivity of the DDS pathway was 22% higher compared to that over catalyst NiMo/TS-1.
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