E-peroxone with a novel GDE decorated with hydrophobic membrane for the degradation of pyridine: Stability, byproducts and toxicity
E-peroxone process is an emerging electrochemical oxidation process, based on ozone and the in-situ cathodic generation of H2O2, but the stability of cathode is one of the key restraining factors. In this study, we designed a multilayer gas diffusion electrode (GDE) decorated with a commercial hydro...
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Veröffentlicht in: | Chemosphere (Oxford) 2024-09, Vol.363, p.142789, Article 142789 |
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Sprache: | eng |
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Zusammenfassung: | E-peroxone process is an emerging electrochemical oxidation process, based on ozone and the in-situ cathodic generation of H2O2, but the stability of cathode is one of the key restraining factors. In this study, we designed a multilayer gas diffusion electrode (GDE) decorated with a commercial hydrophobic membrane for the degradation of pyridine. It was found that a proper control of membrane pore sizes and hot-pressing temperature can significantly promote the GDE stability. Subsequently, key operational parameters of the constructed E-peroxone system were investigated, including the ozone concentration, current density, pH value, electrolyte type and initial concentration of pyridine. The degradation pathways were proposed according to six identified transformation products. The toxicity variation along the degradation progress was evaluated with microbial respiration tests and Toxicity Estimation Software Tool (T.E.S.T.) calculation and an efficient detoxification capacity of E-peroxone was observed. This research provides a theoretical basis and technical support for the development of highly efficient and stable E-peroxone system for the elimination of toxic organic contaminants.
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•The multilayer gas diffusion electrode decorated with PP membrane (0.45μm) shows a stable performance generating H2O2.•The reaction parameters of gas diffusion electrode (GDE) on pyridine degradation were investigated.•The degradation pathways were proposed according to the six identified transformation products.•The acute toxicity of the transformation products was evaluated by the microbial respiration and T.E.S.T. calculation. |
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ISSN: | 0045-6535 1879-1298 1879-1298 |
DOI: | 10.1016/j.chemosphere.2024.142789 |