In this study, natural pyrite (NP) was used to activate peroxydisulfate (PDS) for imidacloprid (IMD) degradation. NP was characterized by X-ray diffraction (XRD), X-ray fluorescence spectrometry (XRF), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). Effects of key reaction parameters (NP dosage, PDS concentration and initial pH) and co-existing ions on IMD degradation in the NP/PDS system were investigated. Quenching experiments and electron spin resonance (ESR) tests identified the existence of sulfate radical (SO4•-), hydroxyl radical (•OH), singlet oxygen (1O2) and superoxide radical (O2•-). The cumulative concentration of SO4•- and •OH were quantified by the formation of benzoquinone (BQ) and p-hydroxybenzoic acid (HBA), respectively. Meanwhile, more than 60% of methylphenyl sulfoxide (PMSO) was selectively converted to methylphenyl sulfone (PMSO2), revealing that Fe(IV) was dominant in the NP/PDS system. The order of contribution of the three reactive species in the NP/PDS system was Fe(IV) > •OH > SO4•- (contributions of 1O2 and O2•- were negligible). Fe(II) released from NP played a crucial role in PDS activation, and sulfur species in NP could also boost Fe(III)/Fe(II) cycle and contribute to the generation of reactive species. Further, the possible degradation pathways of IMD have been proposed based on the detected intermediates using high-performance liquid chromatography-mass spectrometry (HPLC-MS), and the toxicity (including acute toxicity, developmental toxicity and mutagenicity) of these intermediates have been predicted using Toxicity Estimation Software Tool (T.E.S.T). Moreover, NP/PDS system was applied in four natural water bodies and IMD degradation efficiency reached more than 97% after adjusting the pH to 3. The fluorescence excitation-emission matrix (EEM) spectra showed that in addition to IMD, NP/PDS system could also remove other impurities.
Keywords: Degradation pathway; Fe(III)/Fe(II) cycle; Fe(IV); Natural pyrite; Sulfur species.
Copyright © 2022. Published by Elsevier Ltd.