Room-temperature efficient oxidative desulfurization over tungsten doped defective UiO-66 catalyst

被引:3
作者
Shen, Jialing [1 ]
Lv, Guojun [1 ]
Deng, Juan [1 ]
Su, Shihao [1 ]
Wang, Fuxin [1 ]
Xu, Shengnan [1 ]
Oussama, Lachgar [1 ]
Liu, Zhongmin [2 ]
机构
[1] Jiangsu Univ Sci & Technol, Sch Environm & Chem Engn, Zhenjiang 212003, Peoples R China
[2] Dezhou Univ, Sch Chem & Chem Engn, Dezhou 253023, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
UiO-66; Oxidative desulfurization; Zr-O-W bond; METAL-ORGANIC FRAMEWORKS; FUNCTIONALIZED UIO-66; ADSORPTION; REMOVAL; FUEL; OIL;
D O I
10.1016/j.seppur.2025.132299
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
UiO-66 materials have the benefit of excellent stability, porosity, huge surface area, and presence of flaws, hence designing oxidative desulfurization (ODS) catalysts based on UiO-66 is very appealing. Herein, tungsten doped UiO-66 materials were synthesized with post-doping and in situ synthesis methods, and used as heterogeneous catalysts for the room-temperature oxidative desulfurization reactions. The successful doping of tungsten into the UiO-66 framework was demonstrated by FT-IR, UV-Vis, Raman and TGA characterizations. XAS characterization disclosed that tungsten element formed Zr-O-W bond on the defect sites for the tungsten doped UiO-66 materials. At the same time, the in situ synthesized W2@U-150 catalyst revealed the highest 98.5% of dibenzothiophene (DBT) elimination within 1h of desulfurization reaction as well as the biggest catalytic efficiency of 17727.3 h- 1 mol-1 at room temperature due to its smallest band gap energy of 3.32 eV, highest tungsten content of 9.8%, and most Lewis acid amount of 47.1 mu mol/g. In addition, the synthesized W2@U-150 catalyst showed excellent reusability for five cycles.
引用
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页数:12
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