Kinetics and mechanism for oxidative desulfurization of fuels catalyzed by peroxo-molybdenum amino acid complexes in water-immiscible ionic liquids

被引:85
作者
Zhu, WenShuai [1 ]
Li, Huaming [1 ]
Gu, QingQing [1 ]
Wu, Peiwen [1 ]
Zhu, Guopeng [1 ]
Yan, Yongsheng [1 ]
Chen, Guangying [2 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[2] Hainan Normal Univ, Coll Chem & Chem Engn, Haikou 571158, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
Peroxo-molybdenum; Amino acid complexes; Ionic liquid; Extraction; Oxidative desulfurization; ULTRA-DEEP DESULFURIZATION; VACUUM GAS OIL; CHEMICAL OXIDATION; HYDROGEN-PEROXIDE; ROOM-TEMPERATURE; SELECTIVE OXIDATION; SOLVENT-EXTRACTION; EMULSION DROPLETS; MOLECULAR-OXYGEN; DIESEL FUELS;
D O I
10.1016/j.molcata.2010.12.003
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Three peroxo-molybdenum amino acid complexes (PMAACs) were synthesized and characterized. Their catalytic activities for oxidation of dibenzothiophene (DBT) in extraction and catalytic oxidative desulfurization system (ECODS) were evaluated using different ionic liquids. Comparing with simple catalyst Na(2)MoO(4)center dot 2H(2)O in ECODS, PMAACs were effective wide-ranging catalysts and exhibited high desulfurization efficiency not only in water-miscible IL [bmim]BF(4) but also in water-immiscible [bmim]PF(6), [omim]BF(4) and [omim]PF(6). Especially 4,6-dimethyldibenzothiophene (4,6-DMDBT), the most difficult refractory compound in HDS, could be completely removed under optimal conditions. The reaction mechanism and desulfurization differences between using Na(2)MoO(4)center dot 2H(2)O catalyst and PMAACs in water-miscible and water-immiscible ionic liquids have been investigated and explained by UV-vis. Kinetic parameters of the oxidation of DBT, BT and 4,6-DMDBT were studied. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:16 / 22
页数:7
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