Catalytic Oxidative Desulfurization of Fuel by H2O2 In Situ Produced via Oxidation of 2-Propanol

被引:34
|
作者
Zhang, Hong-Xing [1 ,2 ]
Gao, Jia-Jun [1 ,2 ]
Meng, Hong [2 ]
Lu, Ying-zhou [2 ]
Li, Chun-Xi [1 ,2 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Coll Chem Engn, Beijing 100029, Peoples R China
关键词
DEEP DESULFURIZATION; EXTRACTIVE DESULFURIZATION; MOLECULAR-OXYGEN; GASOLINE; EPOXIDATION; THIOPHENE; POLYMERIZATION; OIL; ADSORPTION; GENERATION;
D O I
10.1021/ie300035c
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A novel integrated process is proposed for the catalytic oxidative desulfurization of fuel oil, in which the oxidant H2O2 is in situ generated by oxidizing 2-propanol with oxygen, and its feasibility is evaluated in terms of the S-conversion of 3-methylthiophene (3-MT), benzothiophene (BT), and dibenzothiophene (DBT) in octane under varying conditions. The catalysis of [pi-C5H5NC16H33](3)[PW4O16] is found to be much superior to H3PW12O40 and [(C4H9)(4)N](3)[PW12O40] due to its good dispersivity in oil and adsorptivity for S-compounds. Some influencing factors for the S-conversion were studied, viz., time, temperature, various S-compounds, and the amount of 2-propanol, initiator, oxygen, and catalyst. All factors that favor the production of the 2-propanol radicals affect the desulfurization rate remarkably. Both BT and DBT can be removed efficiently at mild conditions (1.4 MPa O-2, 90 degrees C) in 6 h with S-conversion above 96%, and the resulting sulfones can be separated via settling or filtration.
引用
收藏
页码:4868 / 4874
页数:7
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