Ionic liquid extraction and catalytic oxidative desulfurization of fuels using dialkylpiperidinium tetrachloroferrates catalysts

被引:122
作者
Jiang, Wei [1 ]
Zhu, Wenshuai [1 ]
Chang, Yonghui [1 ,2 ]
Chao, Yanhong [1 ]
Yin, Sheng [1 ]
Liu, Hui [1 ]
Zhu, Fengxia [1 ]
Li, Huaming [1 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[2] Hainan Normal Univ, Sch Chem & Chem Engn, Haikou 571158, Peoples R China
关键词
Dialkylpiperidinium; Tetrachloroferrates; Oxidative desulfurization; H2O2; Ionic liquid; ANDERSON-TYPE CATALYST; DEEP DESULFURIZATION; ROOM-TEMPERATURE; MOLECULAR-OXYGEN; DIESEL FUELS; OIL; DIBENZOTHIOPHENE; ACID; MECHANISM; OXIDANT;
D O I
10.1016/j.cej.2014.03.074
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A new family of dialkylpiperidinium tetrachloroferrate catalysts, such as [C(2)OHmpip]FeCl4, [C(4)mpip]FeCl4, [C(8)mpip]FeCl4, and [C(12)mPip]FeCl4, were synthesized and characterized by FT-IR, Raman, and ESI-MS. Their catalytic activities for oxidation of dibenzothiophene (DBT) in extraction and catalytic oxidative desulfurization system (ECODS) were evaluated using different ionic liquids. Results indicated that the 97.1% removal of DBT was obtained with [C(4)mpip]FeCl4 as catalyst in ionic liquid [C(8)mim]BF4 at 30 degrees C in 60 min. The optimal H2O2/sulfur molar ratio was only 3.5:1, which suggested that the catalyst was one of the most efficient catalysts reported so far. UV-Vis spectra provided an evidence that the lower desulfurization reactivity in PF6--containing ionic liquids was attributed to the strong interaction between ionic liquid and DBT. Through the gas chromatography-mass spectrometer (GC-MS) analysis, dibenzothiophene sulfone was proved to be the only product of oxidation of DBT. Furthermore, the process of ECODS system was confirmed by GC-MS. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:48 / 54
页数:7
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