Electro-enhanced degradation of atrazine via Co-Fe oxide modified graphite felt composite cathode for persulfate activation

过硫酸盐 电化学 煅烧 化学 催化作用 阴极 氧化物 复合数 化学工程 羟基自由基 无机化学 激进的 材料科学 电极 有机化学 复合材料 物理化学 工程类
作者
Xiuping Sun,Zhibin Liu,Zhirong Sun
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:433: 133789-133789 被引量:49
标识
DOI:10.1016/j.cej.2021.133789
摘要

The synergistic activation of persulfate (PS) by electrochemical oxidation (EO) and transition metals has gradually attracted attention as an emerging wastewater method. In this work, a Co-Fe oxide modified graphite felt composite cathode (FeO-CoFeO/GF) was prepared by in-situ solvothermal growth and calcination for PS activation to degrade atrazine (ATZ). The surface morphology, phase composition, microstructure, specific surface area, element valence, and electrochemical properties of the materials were characterized. The EO/FeO-CoFeO/GF + PS system achieved 100% ATZ removal within 35 min and PS was effectively activated by the electrically enhanced FeO-CoFeO/GF compared with other control experiments. The FeO-CoFeO/GF composite cathode exhibited superior catalytic activity in a wide pH range (3–9) and demonstrated good stability in six consecutive cycles. Reactive oxide species were identified by radical quenching tests and electron paramagnetic resonance. Electrochemical oxidation, radical oxidation and non-radical oxidation jointly participate in attacking ATZ. A catalytic mechanism for this synergistic system was proposed to explain PS activation and subsequent ATZ degradation. Furthermore, potential ATZ degradation pathways were proposed. Toxicity changes were evaluated using the Ecological Structure Activity Relationships and Escherichia coli growth inhibition tests. This work provides a feasible strategy for synergistically strengthening PS activation and promoting the degradation of persistent organic pollutants.
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