4.7 Article

Enhanced oxidative desulfurization of liquid model fuel under microwave irradiation over W2N@C catalyst nanoarchitectonics

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 440, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.135841

Keywords

Microwave; Oxidative desulfurization; Porous carbon; Thiophene; Tungsten-nitride

Funding

  1. National Research Foundation of Korea (NRF) - Korean government (MSIT) [NRF-2020R1A4A1018393]

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The quantitative contribution of microwave in oxidative desulfurization (ODS) of liquid fuel was evaluated and found to enhance the reaction rate and lower the activation energy. The catalyst W2N@C exhibited the highest ODS performance under microwave irradiation, with a 3.4 times higher oxidation rate of thiophene compared to conventional electric heating.
Oxidative desulfurization (ODS) of liquid fuel was conducted using a series of W-based catalysts like WO3/ZrO2, WO3/AC, and tungsten-nitride@porous carbon (W2N@C), under both microwave (MW) and conventional electric heating to estimate firstly the quantitative contribution of MW in ODS kinetics. At first, because of the favorable effect of MW on ODS, the most stubborn thiophenic compound, thiophene (Th), could be eliminated (97%) within only 30 min at 60 degrees C under MW irradiation in the presence of the W2N@C catalyst (that showed the highest ODS performance among the studied catalysts). Importantly, the activation energies of Th oxidation over the W2N@C were 22 and 38 kTmol(-1) with microwave and conventional heating, respectively. Moreover, the kinetic constant of Th oxidation with MW was about 3.4 times that of the oxidation with the electric heating at the same temperature (60 degrees C). The rapid kinetics and low E-a under microwave irradiation might be because of the facile formation of reactive superoxide radicals (center dot O-2(-)) (different from the conventional heating where non-radical mechanism prevails) that could be suggested from the oxidations in the presence of radical scavengers and electron spin resonance experiments. The recyclability of the catalyst, after regeneration from oxidation reactions under MW, was also secured, supporting the possible application of W2N@C in removing of thiophenics (especially under MW) from fuel. Finally, MW heating, compared with conventional electric heating, could be recommended as a highly effective strategy for ODS with rapid kinetics and low E-a because of the ready formation of active radicals.

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