Extractive desulfurization of fuel using N-butylpyridinium-based ionic liquids

被引:58
作者
Gao, Hongshuai [1 ]
Zeng, Shaojuan [1 ]
Liu, Xiaomin [1 ]
Nie, Yi [1 ]
Zhang, Xiangping [1 ]
Zhang, Suojiang [1 ]
机构
[1] Chinese Acad Sci, Inst Proc Engn, Key Lab Green Proc & Engn, Beijing Key Lab Ion Liquids Clean Proc, Beijing 100190, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
VACUUM GAS OIL; DEEP-DESULFURIZATION; OXIDATIVE DESULFURIZATION; DIESEL FUEL; DIBENZOTHIOPHENE; DENITROGENATION; GASOLINE;
D O I
10.1039/c5ra03762j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Sulfur compounds in fuels have become one of the sources of serious environmental problems. The extractive desulfurization using ionic liquids (ILs) has attracted great attention in recent years. In this work, the pyridinium-based ionic liquids (ILs) N-butylpyridinium thiocyanate ([C4Py][SCN]), N-butylpyridinium bis(trifluoromethylsulfonyl) imide ([C4Py][NTf2]), and N-butylpyridinium dicyanamide ([C4Py][N(CN)(2)]) were used as extractants for desulfurization of model fuels. The results demonstrate that the structure of the anion influences the extractive performance of ILs, following the order of [NTf2] < [SCN] < [N(CN)(2)], which was proved by the electrostatic interaction between ions and DBT through molecular dynamics simulations (MD). In addition, the selectivity of sulfur compounds by the extraction process followed the order of dibenzothiophene (DBT) > benzothiophene (BT) > 4,6-dimethyldibenzothiophene (4,6-DMDBT). Moreover, the [C4Py][N(CN)(2)] can be recycled at least 4 times with little decrease in the desulfurization activity.
引用
收藏
页码:30234 / 30238
页数:5
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