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Room-temperature efficient oxidative desulfurization over tungsten doped defective UiO-66 catalyst
被引:0
|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:
中国博士后科学基金;
中国国家自然科学基金;
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.
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页数:12
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