碳酸氢盐
刚果红
降级(电信)
氯化物
化学
过氧化氢
激进的
单线态氧
阳极
盐(化学)
膜
离子交换
阴极
核化学
阳离子聚合
电子顺磁共振
吸附
碳纤维
氧气
无机化学
水处理
离子
光催化
光化学
电极
催化作用
电容去离子
电化学
活性染料
水溶液
作者
Tian Zhao,Jiarong Gu,Ziyan Lang,Junjun Ma,Jing Zhang,Jianrui Niu,Situ Mu,Ruina Zhang,Chun Liu,Xiaoxuan CHEN
出处
期刊:ACS ES&T water
[American Chemical Society]
日期:2026-01-16
卷期号:6 (2): 976-988
被引量:1
标识
DOI:10.1021/acsestwater.5c01034
摘要
A novel hybrid semimembrane capacitive deionization (SM-MCDI) system is proposed for the efficient degradation of anionic dye wastewater. Unlike conventional membrane capacitive deionization (MCDI), the SM-MCDI device employs a single cation exchange membrane (CEM) positioned on the cathode side, enabling the direct enrichment of anionic dyes on the anode surface while maintaining charge efficiency. Iron oxide-loaded carbon felt electrodes were used to enhance dye enrichment and catalytic activity. The SM-MCDI system was coupled with peroxymonosulfate (PMS) to promote the in situ oxidative degradation of Congo Red (CR). The effects of the applied voltage, PMS dosage, pH, dye concentration, and coexisting salt ions on CR removal were systematically evaluated. Under optimal conditions (1.2 V, pH 7, 500 mg/L PMS, flow rate of 3 mL/min), 80.84% of 100 mg/L CR was removed within 15 min. Chloride and dihydrogen phosphate ions slightly inhibited CR removal, whereas bicarbonate promoted degradation. Electron paramagnetic resonance analysis confirmed that sulfate radicals (SO 4 ·– ), singlet oxygen ( 1 O 2 ), and hydroxyl radicals ( · OH) were the dominant reactive species. This study demonstrates that the SM-MCDI–PMS strategy enables effective dye degradation and simultaneous salt removal, offering a promising approach for treating complex dye wastewater.
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