Oxidative desulfurization of light gas oil and vacuum gas oil by oxidationand solvent extraction

Citation
S. Otsuki et al., Oxidative desulfurization of light gas oil and vacuum gas oil by oxidationand solvent extraction, ENERG FUEL, 14(6), 2000, pp. 1232-1239
Citations number
31
Categorie Soggetti
Environmental Engineering & Energy
Journal title
ENERGY & FUELS
ISSN journal
08870624 → ACNP
Volume
14
Issue
6
Year of publication
2000
Pages
1232 - 1239
Database
ISI
SICI code
0887-0624(200011/12)14:6<1232:ODOLGO>2.0.ZU;2-W
Abstract
The oxidation of model sulfur compounds (thiophene derivatives, benzothioph ene 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 con ducted with a mixture of hydrogen peroxide and formic acid. The thiophene d erivatives with 5.696 to 5.716 electron densities on the sulfur atoms could not be oxidized at 50 degreesC. Benzo[b]thiophene with 5.739 electron dens ity and other benzothiophene and dibenzothiophenes with higher electron den sities could be oxidized. The sulfur compounds in SR-LGO and VGO appeared t o 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 forme d by oxidation. The removal of sulfur compounds by extraction became more e ffective for the oxidized samples than for the original samples. Lighter su lfur compounds were preferentially extracted. The extraction efficiencies o f solvents, i.e., N,N'-dimethylformamide (DMF), acetonitrile (ACN), methano l, varied greatly. The most effective solvent for the removal of sulfur com pounds was DMF. The recovery of oil was, however, lowest with DMF.