期刊
JOURNAL OF HAZARDOUS MATERIALS
卷 205, 期 -, 页码 164-170出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.jhazmat.2011.12.054
关键词
Oxidative desulfurization; Dibenzothiophene; N-methyl-pyrrolidone; SnCl2; Coordinated ionic liquid; Activation energy
资金
- National Natural Science Foundation of China [21076060, 20806021]
- Natural Science Foundation of Hebei Province [B2009000678]
- Hebei Province Education Department [CPRC022]
A new C5H9NO center dot SnCl2 coordinated ionic liquid (IL) was prepared by reacting N-methyl-pyrrolidone with anhydrous SnCl2. Desulfurization of dibenzothiophene (DBT) via extraction and oxidation with C5H9NO center dot SnCl2 IL as extractant, H2O2 and equal mol of CH3COOH as oxidants was investigated. The Nernst partition coefficients k(N) ofC(5)H(9)NO center dot SnCl2 IL for the DBT in n-octane was above 5.0, showing its excellent extraction ability. During the oxidative desulfurization process, the optimal molar ratio of H2O2/DBT was six. Sulfur removal of DBT in n-octane was 94.8% in 30 min at 30 degrees C under the conditions of H2O2/DBT molar ratio of six and V (IL):V (oil) = 1:3. Moreover, the sulfur removal increased with increasing temperature because of the high reaction rate constant, low viscosity, and high solubility of dibenzothiophene-sulfone in the IL The kinetics of oxidative desulfurization of DBT was also investigated, and the apparent activation energy was found to be 32.5 kJ/mol. The IL could be recycled six times without a significant decrease in activity. (C) 2011 Elsevier B.V. All rights reserved.
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