Synergistic activation of persulfate by natural chalcocite and ferrous ions by promoting the cycling of Fe3+/Fe2+ couple for degradation of organic pollutants

Natural chalcocite (NCC) was chosen as a co-catalyst for activation of persulfate (PS) to degrade organic contaminants in this study. A synergistic effect between NCC and ferrous ions (Fe2+) was found in catalyzing PS for degradation of orange G (OG). The main role of NCC in the NCC/Fe2+/PS system was to facilitate Fe3+ reduction back to Fe2+ and thus improve the stoichiometric efficiency of PS. The results of scavenging experiments and electron paramagnetic resonance tests proved that both sulfate and hydroxyl radicals were the primary reactive oxidants in the NCC/Fe2+/PS system. Twelve potential intermediate products of OG were identified, and the degradation pathway was proposed. Experiment parameters, such as NCC dose, Fe2+ concentration, initial pH, and the presence of anions (H2PO4- and Cl-) all had important impacts on OG degradation. NCC had good reusability in synergistic activation of PS with Fe2+ for OG degradation for five cycles. This study demonstrated a natural sulfide mineral as an efficient co-catalyst towards PS activation for destruction of organic contaminants in water.

Automated summary

This study demonstrated that natural chalcocite can serve as an efficient co-catalyst for the activation of persulfate in degrading organic contaminants. The synergistic effect between NCC and Fe2+ in catalyzing PS for degradation of orange G was identified. Parameters such as NCC dose, Fe2+ concentration, initial pH, and the presence of anions were found to have important impacts on OG degradation. NCC showed good reusability in synergistic activation of PS with Fe2+ for OG degradation over five cycles.