Preparation of g-C3N4 supported phosphotungstate hybrid materials and their catalytic performance in the oxidative desulfurization
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Abstract
A series of supported Bmim3PW12O40/g-C3N4 catalysts (BPWO/g-C3N4) was prepared by coprecipitation, with 1-butyl-3-methylimidazole bromide, phosphotungstic acid and g-C3N4 as the raw materials. The morphology and structure of the BPWO/g-C3N4 catalysts were characterized by XRD, FT-IR, UV-vis, N2 physisorption, TEM and XPS; the effects of catalyst composition, oxygen to sulfur (O/S) ratio, catalyst amount and reaction temperature on the oxidative desulphurization efficiency were investigated by using n-heptane solution of dibenzothiophene (DBT) as a model oil and hydrogen peroxide as the oxidant. The results indicate that the BPWO/g-C3N4 catalysts have a Keggin-type heteropoly anionic structure and BPWO is well dispersed on g-C3N4. The BPWO(20%, mass ratio)/g-C3N4 catalyst exhibits the optimal oxidation performance towards DBT. Under 50℃ and with a O/S molar ratio of 6.0, DBT in the model oil with a concentration of 800 μg/g can be completely oxidized over the BPWO(20%, mass tatio)/g-C3N4 catalyst in 180 min. Moreover, the BPWO(20%, mass ratio)/g-C3N4 catalyst displays a good reusability and can be recycled for at least 8 cycles without any decrease in the DBT oxidation activity.
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