The electrocatalytic degradation of 1,4-dioxane by Co–Bi/GAC particle electrode
Efficient degradation of industrial organic wastewater has become a significant environmental concern. Electrochemical oxidation technology is promising due to its high catalytic degradation ability. In this study, Co-Bi/GAC particle electrodes were prepared and characterized for degradation of 1,4-dioxane. The electrochemical process parameters were optimized by response surface methodology (RSM), and the influence of water quality factors on the removal rate of 1,4-dioxane was investigated. The results showed that the main influencing factors were the Co/Bi mass ratio and calcination temperature. The carrier metals, Co and Bi, existed mainly on the GAC surface as Co<sub>3</sub>O<sub>4</sub> and Bi<sub>2</sub>O<sub>3</sub>. The removal of 1,4-dioxane was predominantly achieved through the synergistic reaction of electrode adsorption, anodic oxidation, and particle electrode oxidation, with ·OH playing a significant role as the main active free radical. Furthermore, the particle electrode was demonstrated in different acid-base conditions (pH = 3, 5, 7, 9, and 11). However, high concentrations of Cl<sup>-</sup> and NO<sub>3</sub><sup>-</sup> hindered the degradation process, potentially participating in competitive reactions. Despite this, the particle electrode exhibited good stability after five cycles. The results provide a new perspective for constructing efficient and stable three-dimensional (3D) electrocatalytic particle electrodes to remove complex industrial wastewater.
Authors
- Chao Ma (ORCID: https://orcid.org/0000-0001-8599-9340)
- Zhineng Dai
- Rui Wang (ORCID: https://orcid.org/0009-0007-5995-2099)
- Wenqi Zhang (ORCID: https://orcid.org/0009-0002-5530-0353)
Institutions
- Xiamen University (CN)
- Xiamen University of Technology (CN)
Publication Details
- Journal
- Water Science & Technology
- Published
- 2024-08-12
- DOI
- https://doi.org/10.2166/wst.2024.274
- Primary Topic
- Advanced oxidation water treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00