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
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.