| Literature DB >> 29807239 |
Yuanyuan Chu1, Xiaoyao Tan2, Zhangfeng Shen3, Pengyun Liu3, Ning Han3, Jian Kang3, Xiaoguang Duan3, Shaobin Wang4, Lihong Liu5, Shaomin Liu3.
Abstract
Removal of toxic organics and bacterial disinfection are important tasks in wastewater treatment. Most heavy metal-based catalysts for degradation of aqueous organic pollutants in heterogeneous Fenton-like processes suffer from the toxicity of leached metals. The present work reports environmentally benign systems for both degradation of organics and bacterial disinfection. Calcium substituted LaFeO3-δ perovskite was demonstrated as an efficient catalyst to activate peroxymonosulfate (PMS) for degradation of phenol, methylene blue and rhodamine 6 G. Compared to LaFeO3-δ and nanocrystal Fe3O4, the lattice oxygen vacancies in B-site cation-deficient perovskite of La0.8Ca0.2Fe0.94O3-δ (LaCaFeO3-δ) particles renders this material a greatly improved catalytic performance. Electron paramagnetic resonance (EPR) suggested that both sulfate (SO4-) and hydroxyl radicals (OH) played critical roles in the advanced oxidation processes. Moreover, silver doped perovskite (Ag-LaCaFeO3-δ)/PMS successfully inhibited the growth of waterborne pathogen Escherichia coli and Methicillin-resistant Staphylococcus aureus (MRSA) at a lower dose than silver ions, proving a synergetic effect between free radicals and Ag+ in killing the bacteria. Therefore, Ag-LaCaFeO3-δ/PMS would be promising for practical wastewater treatment.Entities:
Keywords: Cobalt-free perovskite catalyst; Microbial disinfection; Organic degradation; Peroxymonosulfate oxidation
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Year: 2018 PMID: 29807239 DOI: 10.1016/j.jhazmat.2018.05.044
Source DB: PubMed Journal: J Hazard Mater ISSN: 0304-3894 Impact factor: 10.588