4.7 Article

Simultaneous electrochemical oxidation and ferrate generation for the treatment of atrazine: A novel process for water treatment applications

期刊

JOURNAL OF HAZARDOUS MATERIALS
卷 411, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.jhazmat.2021.125167

关键词

Electrochemical oxidation; Ferrate; Atrazine; Water treatment; Boron doped diamond; Electro-oxidation

资金

  1. Imperial College London
  2. Natural Sciences and Engineering Research Council of Canada (NSERC) [PGSD3516562-2018]

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A novel process involving simultaneous electrochemical-oxidation and electrosynthesis of ferrate was investigated for the treatment of atrazine, a commonly detected and recalcitrant pesticide. The synthesis of ferrate was affected by initial iron concentration, with higher concentrations resulting in higher ferrate generation. Additionally, the degradation of atrazine using electrochemically-generated ferrate showed a higher degradation rate constant compared to solely electrochemical oxidation processes.
A novel process involving the simultaneous electrochemical-oxidation (EO) and electrosynthesis of ferrate has been investigated for the treatment of the commonly detected and recalcitrant pesticide, atrazine. The present study considered the electrosynthesis of ferrate, in neutral pH, using low concentration iron (Fe2+) representative of raw water levels and its subsequent effect on atrazine degradation. Ferrate synthesis was unaffected by current density (10?80 mA cm-2), indicating mass transport limitations. Synthesis was affected by the initial iron concentration, whereby 0.051, 0.108 and 0.332 mg L-1 was generated with an Fe2+ concentration of 0.5, 1.0 and 3.0 mg L-1, respectively. When operating under simultaneous EO and ferrate oxidation, atrazine degradation exceeded that of a solely EO process. From an initial concentration of 2.00 mg L-1, atrazine was degraded to 1.34, 1.05 and 0.51 mg L-1 during 10, 40 and 80 mA cm-2, characterised by pseudo-first-order kinetics. Degradation with electrochemically-generated ferrate could be described by second-order kinetics, and yielded a degradation rate constant of 23.5 M-1 s-1. The effect of natural organic matter (NOM) on atrazine degradation was also investigated. Ferrate was observed to be mostly scavenged by resorcinol, a representative NOM compound, having a second-order reaction rate constant of 9.71 ? 102 M-1 s-1.

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