Oxidative Desulfurization of Light Gas Oil and Vacuum Gas Oil by Oxidation and Solvent Extraction

苯并噻吩 二苯并噻吩 噻吩 化学 硫黄 减压蒸馏 烟气脱硫 有机化学 溶剂 过氧化氢 甲酸 蒸馏 核化学 无机化学
作者
Shujiro Otsuki,Takeshi NONAKA,Noriko Takashima,Eika W. Qian,Atsushi Ishihara,Tamotsu Imai,Toshiaki Kabe
出处
期刊:Energy & Fuels [American Chemical Society]
卷期号:14 (6): 1232-1239 被引量:928
标识
DOI:10.1021/ef000096i
摘要

The oxidation of model sulfur compounds (thiophene derivatives, benzothiophene derivatives, and dibenzothiophene derivatives), straight run-light gas oil (SR-LGO, S: 1.35 wt %), and vacuum gas oil (VGO, S: 2.17 wt %) were conducted with a mixture of hydrogen peroxide and formic acid. The thiophene derivatives with 5.696 to 5.716 electron densities on the sulfur atoms could not be oxidized at 50 °C. Benzo[b]thiophene with 5.739 electron density and other benzothiophene and dibenzothiophenes with higher electron densities could be oxidized. The sulfur compounds in SR-LGO and VGO appeared to be oxidized to a detectable levels (c.a., 0.01 wt % S) by GC-FPD analysis. The IR spectra of oxidized SR-LGO and VGO showed that sulfones were formed by oxidation. The removal of sulfur compounds by extraction became more effective for the oxidized samples than for the original samples. Lighter sulfur compounds were preferentially extracted. The extraction efficiencies of solvents, i.e., N,N'-dimethylformamide (DMF), acetonitrile (ACN), methanol, varied greatly. The most effective solvent for the removal of sulfur compounds was DMF. The recovery of oil was, however, lowest with DMF.
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