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Nature Communications· 2018Q1

Electrochemically-mediated selective capture of heavy metal chromium and arsenic oxyanions from water

Xiao Su, Akihiro Kushima, Cameron Halliday, Jian Zhou et al.

Short summary

Redox-active metallopolymer electrodes electrochemically capture chromium and arsenic oxyanions with high selectivity, achieving >100 mg Cr/g adsorbent and 99% reversible capacity.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Metallopolymer electrodes electrochemically capture chromium and arsenic oxyanions.
  • Uptake capacity exceeds 100 mg Cr/g adsorbent with 99% reversible working capacity.
  • Chromium is released in the less harmful trivalent form.
  • Selective removal is achieved at concentrations as low as 100 ppb, even with >200-fold excess salts.
  • Mechanism involves strong charge transfer to heavy metal oxyanions.

AI-generated from the title and abstract; the full text is not read.

Abstract

The removal of highly toxic, ultra-dilute contaminants of concern has been a primary challenge for clean water technologies. Chromium and arsenic are among the most prevalent heavy metal pollutants in urban and agricultural waters, with current separation processes having severe limitations due to lack of molecular selectivity. Here, we report redox-active metallopolymer electrodes for the selective electrochemical removal of chromium and arsenic. An uptake greater than 100 mg Cr/g adsorbent can be achieved electrochemically, with a 99% reversible working capacity, with the bound chromium ions released in the less harmful trivalent form. Furthermore, we study the metallopolymer response during electrochemical modulation by in situ transmission electron microscopy. The underlying mechanisms for molecular selectivity are investigated through electronic structure calculations, indicating a strong charge transfer to the heavy metal oxyanions. Finally, chromium and arsenic are remediated efficiently at concentrations as low as 100 ppb, in the presence of over 200-fold excess competing salts.

The authors' abstract, as published at the source. Nature Communications, 2018 · DOI ↗

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Field: Electrochemistry

ElectrochemistryChemistry