| Literature DB >> 31855755 |
Yanbiao Liu1, Jie Zhang2, Fuqiang Liu2, Chensi Shen3, Fang Li4, Manghong Huang3, Bo Yang2, Zhiwei Wang5, Wolfgang Sand6.
Abstract
Environmental pollution caused by antimony (Sb) has attracted worldwide attention recently. Here, we employed a flow-through electro-Fenton system for the rapid and efficient detoxification of highly toxic Sb(III). A FeOCl modified carbon nanotube (CNT) filter served as functional cathode, where FeOCl as nanocatalyst promoted the generation of HO by facilitating effective Fe3+/Fe2+ cycling. Upon application of a proper potential, an ultra-rapid conversion of Sb(III) to less toxic Sb(V) can be achieved in situ just by a single-pass filtration (>99% within 2 s). Compared with the conventional batch reactor, the proposed system demonstrated ultra-rapid Sb(III) detoxification kinetics due to the convection-enhanced mass transport. The proposed flow-through E-Fenton system works effectively across a wide pH range (e.g., 3-9). EPR technique and radical quenching experiments indicate that HO and HO2 were the dominant radical species responsible for Sb(III) detoxification. At -0.4 V vs. Ag/AgCl, a >96.4% Sb(III) conversion efficiency still can be achieved when challenged with 500 μg L-1 Sb(III)-spiked tap water. The as-produced Sb(V) can be removed effectively by another Sb(V)-specific CNT filter functionalized with nanoscale iron oxides. The outcome of this research provides a promising strategy by integrating state-of-the-art electro-Fenton, membrane separation, carboncatalysis and nanotechnology for detoxification of Sb(III) and other similar heavy metal ions in polluted water.Entities:
Keywords: Antimony; Electro-fenton; Flow-through; Hydroxyl radical; Iron oxychloride
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Year: 2019 PMID: 31855755 DOI: 10.1016/j.chemosphere.2019.125604
Source DB: PubMed Journal: Chemosphere ISSN: 0045-6535 Impact factor: 7.086