Preparation of di-[EMIM]CoCl3 Ionic Liquid Catalyst and Coupling with Oxone for Desulfurization at Room Temperature

Author:

Wang Shaokang1,Xu Hang12

Affiliation:

1. School of Chemistry and Chemical Engineering, Henan University of Science and Technology, Luoyang 471023, China

2. Provincial and Ministerial Co-Construction of Collaborative Innovation Center for Non-Ferrous Metal New Materials and Advanced Processing Technology, Luoyang 471023, China

Abstract

The intermediate di-[EMIM]Cl was synthesized from methyl imidazole and 1,4-dichlorobutane and then reacted with cobalt chloride at 105 °C to prepare a bi-[EMIM]CoCl3 ionic liquid catalyst. The di-[EMIM]CoCl3 catalyst coupled with oxone to remove sulfur-containing organics in octane. The di-[EMIM]CoCl3 catalyst was characterized by HNMR, FTIR, TG, and SEM–EDS. The dibenzothiophene (DBT) was dissolved in octane to prepare a model oil with an initial sulfur content of 500 ppm. Six grams of the model oil was added. The results showed that the optimal dosages of di-[EMIM]CoCl3, oxone (20 wt%), and [BMIM]BF4 extractant were 1 g, 2 g, and 2 g, respectively. At the optimum temperature of 45 °C, 100% of sulfur was removed after 40 min. After di-[EMIM]CoCl3 was recycled five times, the sulfur removal percentage remained above 91%. The sulfur removal percentages for different sulfur-containing organics followed the order of dibenzothiophene (DBT) > benzothiophene (BT) > 4,6-dimethyldibenzothiophene (4,6-DMDBT). The oxidation product was determined to be DBTO2 by GC–MS analysis, and the oxidation mechanism was discussed. The active oxygen atoms of oxone oxidized DBT to form DBTO, and then persulfate oxidized DBTO to DBTO2 via an identical oxidation mechanism.

Funder

Nature Science Foundation of Henan Province

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Catalysis,General Environmental Science

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