
@Article{jrm.2022.018474,
AUTHOR = {Jinglong Huai, Xiaoxue Liu, Yinhai Zhang, Yang Yang, Yan Gou, Li Qin, Jinling Shan, Yancheng Zheng, Hao Li},
TITLE = {Synthesis of Hierarchical TS-1 and Its Recycling Catalytic Property for Oxidative Desulfurization},
JOURNAL = {Journal of Renewable Materials},
VOLUME = {10},
YEAR = {2022},
NUMBER = {6},
PAGES = {1711--1726},
URL = {http://www.techscience.com/jrm/v10n6/46589},
ISSN = {2164-6341},
ABSTRACT = {Because of its unique pore structure, good hydrothermal stability and high specific surface area, hierarchical TS-1 zeolite (HTS-1) has become an important catalyst for the deep oxidative desulfurization of fuel oils. In this work, HTS-1 has been successfully synthesized by a hydrothermal crystallization method using the C-SiO<sub>2</sub> composite as both silicon source and mesoporous template, tetrapropylammonium hydroxide as microporous template, and tetrabutylorthotitanate as titanium source. The C-SiO<sub>2</sub> composite is obtained by mild carbonization of the SiO<sub>2</sub>/T-40 (Tween 40) xerogel, which is prepared by the two step sol-gel method. The reaction conditions for the oxidative desulfurization (ODS) of dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (4,6-DMDBT) over HTS-1 are optimized systematically, and the recycling performances of HTS-1 are investigated in detail. After the 15th run, HTS-1 still maintains high DBT conversion (90.6%) and 4,6-DMDBT conversion (86.0%) without deactivation. The samples before and after recycle tests are characterized by XRD, FT-IR, CHN analysis, UV-Vis and SEM techniques. The results indicate that the crystal structure and morphology of regenerated HTS-1 samples are well kept, which accounts for the good structural stability and reusability of HTS-1. In addition, active intermediates for the ODS of bulky organic sulfides over HTS-1, i.e., Ti-peroxo (Ti-OO<sup>t</sup>Bu) species, are captured by the UV-Vis technique. Finally, a possible reaction mechanism for the ODS process over HTS-1 is proposed.},
DOI = {10.32604/jrm.2022.018474}
}



