Modified W, Ti-doped IrO2 anode for efficient organic contaminant oxidation in livestock wastewater

阳极 化学 电解 废水 催化作用 化学需氧量 电化学 电催化剂 无机化学 电解质 化学工程 核化学 环境化学 电极 环境工程 有机化学 环境科学 工程类 物理化学
作者
Yiheng Zhang,Lin Zhu,Xin Guo,Wenjing Zhang,Xiang Shao,Ji Yang
出处
期刊:Journal of Electroanalytical Chemistry [Elsevier BV]
卷期号:931: 117192-117192 被引量:13
标识
DOI:10.1016/j.jelechem.2023.117192
摘要

The treatment of livestock wastewater is a major environmental challenge due to the presence of antibiotics from animal excreta, which may pass through conventional biological oxidation treatment and pose a threat to public health. Electro-oxidation method presents an opportunity to remove antibiotics in the livestock wastewater at the source of generation, and titanium-based IrO2 anode has been shown to have excellent electro-catalytic activity and stability. However, the soaring price of iridium limits the practical application. In this work, we showed that W, Ti-doped IrO2 anodes largely preserved the electro-catalytic activity while reducing the cost of electrode fabrication. The prepared Ti/Sb-SnO2/(Ir0.6W0.2Ti0.2)Ox anode was shown to achieve 94 % conversion of sulfadiazine in 1 min and 100 % conversion in 15 min. Additionally, complete removal of chemical oxygen demand (COD0 = 700–800 mg/L) was achieved in 1–3 h of electrolysis at 40 mA/cm2. Chlorine-mediated oxidation was demonstrated to be the main mechanism for organic contaminant degradation. The COD removal during galvanostatic electrolysis exhibited zero-order kinetics, indicating that the reaction rate was controlled by the heterogeneous reaction at the anode surface. In the stability test, >95 % COD removal was maintained after 5 cycles of electro-oxidation experiments. The accelerated life of the anode was tested to be 352 h (1000 mA/cm2, 1 M H2SO4 electrolyte, 60 °C).
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