二苯并噻吩
催化作用
烟气脱硫
X射线光电子能谱
傅里叶变换红外光谱
化学
扫描电子显微镜
介孔材料
核化学
材料科学
化学工程
有机化学
工程类
复合材料
作者
Yongcong Ding,Jian Wang,Mingyu Liao,Jiachun Li,Linfeng Zhang,Jia Guo,Huadong Wu
标识
DOI:10.1016/j.cej.2021.129470
摘要
Oxidative desulfurization (ODS) process is one of the most promising desulfurization technologies because of its energy-efficient and mild operation condition. In this study, a novel active phase POM-based IL-[Omim]3PMo12O40 was synthesized, and then it was supported on well-ordered KIT-6. [Omim]3PMo12O40/KIT-6 catalyst was used in the dibenzothiophene (DBT) and real diesel oxidative desulfurization with tertbutyl hydroperoxide (TBHP) as an oxidant. The composite materials [Omim]3PMo12O40 and [Omim]3PMo12O40/KIT-6 catalysts were characterized by means of Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), X-ray photo-electron spectroscopy (XPS) and nitrogen adsorption–desorption analysis. [Omim]3PMo12O40/KIT-6 catalyst showed high catalytic activity, at the optimal conditions of mcatalyst/VOil = 0.1 g/20 ml, m[Omim]3PMo12O40/mKIT-6 = 30%, O/S = 5 (molar ratio), 60 °C, S of 1000 ppm (DBT in n-octane) can be completely removed within 80 min due to the superior mass transfer ability of the cubic Ia3_d mesoporous structure of KIT-6 and excellent catalytic ability of [Omim]3PMo12O40. In addition, [Omim]3PMo12O40/KIT-6 could be easily separated and the catalytic activity remains stable after 9 cycles. The ODS reaction mechanism is also investigated.
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