Deep eutectic solvents (DESs) have been extensively studied as promising green solvents to attain a better removal efficiency of sulfide. A new DES system formed from choline chloride (ChCl), benzene sulfonic acid (BSA), and ethylene glycol (EG) as a class of ternary DESs was prepared and used in the oxidative desulfurization (ODS) of different sulfides. Ternary DESs have distinct advantages such as volatility and high activity compared with organic acid-based binary DESs. Under the optimum conditions with VDES/VOil = 1 : 5, O/S (molar ratio of oxygen to sulfur) = 5, and T = 25 °C, the desulfurization efficiencies of dibenzothiophene (DBT), 4,6-dimethyldibenzothiophene (4,6-DMDBT), and benzothiophene (BT) were all achieved to 100% in 2 h. Through experimental and density functional theory (DFT) calculation methods, this new system as a class of ternary DESs shows good stability and excellent desulfurization performance at room temperature. The investigation of this study could supply a new idea of ternary DESs for oxidative desulfurization.
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