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Nickel-foam-supported β-Ni(OH)2 as a green anodic catalyst for energy efficient electrooxidative degradation of azo-dye wastewater

  • Shan Sun
  • , Peng Diao*
  • , Cuiyun Feng
  • , Eleonora Mihaela Ungureanu
  • , Yi Tang
  • , Bin Hu
  • , Qing Hu
  • *Corresponding author for this work
  • School of Materials Science and Engineering
  • Beihang University
  • Department of Physical Chemistry and Electrochemistry
  • National University of Science and Technology POLITEHNICA Bucharest
  • Southern University of Science and Technology

Research output: Contribution to journal › Article › peer-review

Abstract

Electrochemical oxidative degradation (EOD) is a particularly promising technique for removing organic pollutants from wastewater. However, due to the high overpotential of EOD in conventional anode materials, the energy cost of EOD is usually very high, which greatly promotes the search for highly active, stable, and energy-efficient anodic catalysts. Herein, we demonstrated that nickel-foam-supported (NF-supported) β-Ni(OH)2 (NF/β-Ni(OH)2) prepared via a facile hydrothermal method could be used as an energy efficient anode for EOD. The as-prepared 3D porous NF/β-Ni(OH)2 exhibited high activity toward the electrochemical oxidation of methyl orange (MO) in the low potential region (<1.07 V vs. SCE). This property differs greatly from those of the conventional anode materials that require a high positive potential to keep them active for EOD, making NF/β-Ni(OH)2 an energy-efficient and active anode material for EOD. With an oxidation current density of 0.25 mA cm-2, the decolorization of MO was completed within 30 min, and the COD removal after 3h of reaction was 63.0%. The normalized energy consumption for the 3 h degradation of MO was 22.2 kW h (kg COD)-1, which is only a fraction of (or even one tenth of) the values reported in the literature. Moreover, NF/β-Ni(OH)2 had a good stability and recyclability for EOD. No activity decay was observed during 10 h of EOD and the COD removal remained almost unchanged after four consecutive reaction cycles. We demonstrated experimentally that the NF/β-Ni(OH)2 anode could generate large amounts of hydroxyl radicals and that the oxidation of MO by hydroxyl radicals was the main mechanism during EOD. We believe that this work opens a new avenue for developing highly active and energy-efficient anode materials that can work in the low potential region for EOD.

Original languageEnglish
Pages (from-to)19776-19785
Number of pages10
JournalRSC Advances
Volume8
Issue number35
DOIs
StatePublished - 2018

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

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