Key Laboratory of Water and Sediment Sciences of Ministry of Education, State Key Laboratory of Water Environment Simulation, School of Environment, Beijing Normal University, Beijing, 100875, PR China; Key Laboratory of Coastal Biology and Utilization, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai, Shandong, 264003, PR China.
Key Laboratory of Water and Sediment Sciences of Ministry of Education, State Key Laboratory of Water Environment Simulation, School of Environment, Beijing Normal University, Beijing, 100875, PR China.
Chemosphere. 2019 Feb;217:800-807. doi: 10.1016/j.chemosphere.2018.11.077. Epub 2018 Nov 13.
Advanced oxidation process (AOP) based on peroxymonosulfate (PMS) activation was established in microbial fuel cell (MFC) system with MnFeO cathode (MFC-MnFeO/PMS) aimed to enhance azo dye degradation and catalyst regeneration. The effects of loading amount of MnFeO catalyst, applied voltage, catholyte pH and PMS dosage on the degradation of Orange II were investigated. The stability of the MnFeO cathode for successive PMS activation was also evaluated. The degradation of Orange was accelerated in the MFC-MnFeO/PMS with apparent degradation rate constant increased to 1.8 times of that in the MnFeO/PMS control. A nearly complete removal of Orange II (100 mg L) was attained in the MFC-MnFeO/PMS under the optimum conditions of 2 mM PMS, 10 mg cm MnFeO loading, pH 7-8 and 480 min reaction time. MFC driven also extended the longevity of the MnFeO catalyst for PMS activation due to the in-situ regeneration of ≡Mn and ≡Fe through accepting electrons from the cathode, and over 80% of Orange II was still removed in the 7 run. Additionally, the MFC-MnFeO/PMS system could recover electricity during Orange II degradation with a maximum power density of 206.2 ± 3.1 mW m. PMS activation by MnFeO was the primary pathway for SO generation, and SO based oxidation was the primary mechanism for Orange II degradation. MFCs driven coupled with PMS activated AOP systems provides a novel strategy for efficient and persistent azo dye degradation.
基于过一硫酸盐 (PMS) 活化的高级氧化工艺 (AOP) 在微生物燃料电池 (MFC) 系统中与 MnFeO 阴极 (MFC-MnFeO/PMS) 结合,旨在增强偶氮染料降解和催化剂再生。研究了 MnFeO 催化剂负载量、施加电压、阴极液 pH 值和 PMS 剂量对橙色 II 降解的影响。还评估了 MnFeO 阴极对连续 PMS 活化的稳定性。在 MFC-MnFeO/PMS 中,橙色的降解速度明显加快,表观降解速率常数提高到 MnFeO/PMS 对照的 1.8 倍。在最佳条件下,即 2 mM PMS、10 mg cm MnFeO 负载量、pH 值 7-8 和 480 min 反应时间,MFC-MnFeO/PMS 可实现 Orange II 的近乎完全去除(100 mg L)。由于通过从阴极接受电子,≡Mn 和 ≡Fe 原位再生,MFC 驱动还延长了 MnFeO 催化剂用于 PMS 活化的寿命,在 7 次运行中,仍有超过 80%的 Orange II 被去除。此外,MFC-MnFeO/PMS 系统可以在 Orange II 降解过程中回收电能,最大功率密度为 206.2 ± 3.1 mW m。MnFeO 对 PMS 的活化是 SO 生成的主要途径,SO 基氧化是 Orange II 降解的主要机制。MFC 驱动与 PMS 激活的 AOP 系统相结合,为高效持久地降解偶氮染料提供了一种新策略。