Abstract

Abstract Without external O2 supply and solution pH adjusting, commercial molybdenum sulfide (MoS2) was firstly applied as co-catalyst in intermittent electro-Fenton process for Rhodamine B (RhB) degradation. In this energy saving system, Fe2+/Fe3+ conversion was facilitated and H2O2 activating was accelerated by MoS2. Granular activated carbon wrapped with stainless steel mesh (GACSS) was used as cathode, from which, H2O2 and iron sources were in-situ generated. With 0.1 g/L MoS2, and 50 mA applied current with 10 min on-10 min off power frequency, RhB degradation rate constant in the MoS2 intermittent electro-Fenton was approximately 2.4 times as that without MoS2 system. Quenching experiments, electron spin resonance (ESR) characterization and free radical fluorescence tests demonstrated hydroxyl radicals (·OH) was the dominant reactive species, and the superiority of intermittent electrolysis mode for RhB degradation. During power on, H2O2 was constantly generated on cathode. In electricity interval, Fe2+/Fe3+ conversion was accelerated on the active sites (Mo4+) to activate residual H2O2 and more ·OH was generated to RhB degradation. Additionally, the characterization analysis (XPS, SEM and FT-IR) demonstrated MoS2 and GACSS cathode exhibited excellent catalytic and chemical stability in recyclability. Low-cost multifunctional cathode with a high efficiency co-catalyst was combined in this energy saving electro-Fenton operating system for RhB degradation.

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