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在室温条件下,MnO/石墨毡上的 O 的电激活用于高效氧化水中污染物。

Electro-activation of O on MnO/graphite felt for efficient oxidation of water contaminants under room condition.

机构信息

Anhui Province Key Laboratory of Advanced Catalytic Materials and Reaction, School of Chemistry and Chemical Engineering, Hefei University of Technology, Hefei, 230009, China.

Institute of Industry & Equipment Technology, Hefei University of Technology, Hefei, 230009, China.

出版信息

Chemosphere. 2019 Nov;234:269-276. doi: 10.1016/j.chemosphere.2019.06.083. Epub 2019 Jun 11.

Abstract

The activation of oxygen (O) under room condition is highly desirable for oxidative removal of organic pollutants in water. Herein, we report a graphite felt (GF)-supported α-MnO catalyst which is active for activating O with assistance of an anodic electric field. The electro-assisted catalytic wet air oxidation (ECWAO) process on MnO/GF is able to rapidly degrade a variety of dyes, pharmaceutics and personal care products (PPCPs) under room condition. The congo red, basic fuchsin, neutral red and methylene blue are completely mineralized in 160 min, and the bisphenol A, triclosan and ciprofloxacin are mineralized by 89.9%, 81.5% and 65.4%, respectively, in 300 min. Mechanistic study indicates a surface-catalyzed non-free radical pathway for the oxidation of organic pollutants by O in the ECWAO process. The oxygen vacancies on MnO are identified as the catalytically active sites, at which oxygen atom is transferred from O to organic molecule through chemisorbed oxygen species. The anodic electric field assists such an oxygen transfer pathway by activating the complex of chemisorbed oxygen species and organic molecule through electro-oxidation reaction. The ECWAO process on MnO/GF electrode exhibits a great potential for practical wastewater treatment under room condition.

摘要

在室温条件下激活氧气(O)对于水中有机污染物的氧化去除是非常理想的。在此,我们报告了一种石墨毡(GF)负载的α-MnO 催化剂,在阳极电场的辅助下,该催化剂能够有效地激活 O。MnO/GF 的电辅助催化湿式空气氧化(ECWAO)过程能够在室温条件下快速降解各种染料、药物和个人护理产品(PPCPs)。刚果红、碱性品红、中性红和亚甲基蓝在 160 分钟内完全矿化,双酚 A、三氯生和环丙沙星分别在 300 分钟内矿化 89.9%、81.5%和 65.4%。机理研究表明,在 ECWAO 过程中,O 通过表面催化非自由基途径氧化有机污染物。MnO 上的氧空位被确定为催化活性位,在该活性位上,氧原子通过化学吸附氧物种从 O 转移到有机分子。阳极电场通过电氧化反应激活化学吸附氧物种和有机分子的复合物,从而辅助这种氧转移途径。MnO/GF 电极上的 ECWAO 过程在室温条件下具有实际废水处理的巨大潜力。

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