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首页> 外文期刊>Electrochimica Acta >Mechanism for enhancing biodegradability of antibiotic pharmacy wastewater by in-situ generation of H2O2 and radicals over MnOxano-G/2-EAQ/AC cathode
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Mechanism for enhancing biodegradability of antibiotic pharmacy wastewater by in-situ generation of H2O2 and radicals over MnOxano-G/2-EAQ/AC cathode

机译:MnOx / nano-G / 2-EAQ / AC阴极原位生成H2O2和自由基增强抗生素制药废水生物降解性的机理

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To improve the oxidation efficiency of cathode in the electrochemical advanced oxidation processes (EAOPs), the manganese oxideano-graphite (MnOxano-G) was synthesized via a liquid-phase precipitation method. Structure and property of MnOxano-G calcined at different temperatures (350, 450 and 550 degrees C) were investigated. Results showed that nano-G ashing and MnOx agglomeration were happened at 550 degrees C. MnOxano-G calcined at 450 degrees C was proved to have the highest efficiency for phenol degradation. The valences of Mn in the MnOxano-G (450 degrees C) were + 3 (Mn2O3) and + 4 (MnO2). Activity of the prepared MnOxano-G/2-ethylanthraquinone/activated carbon (MnOxano-G/2-EAQ/AC) cathode was investigated through evaluating H2O2 and (OH)-O-center dot yields, phenol degradation with scavengers, and impedances. 2-EAQ and MnOx could promote the two-electron reduction of O-2 (H2O2) and the generation of (OH)-O-center dot radicals, respectively. After 6 h electrolysis, the biodegradability (BOD5/COD) of antibiotic pharmacy wastewater was improved from 0.01 to 0.31, indicating that MnOxano-G/2-EAQ/ AC cathode had promise for further application. (C) 2016 Elsevier Ltd. All rights reserved.
机译:为了提高电化学高级氧化工艺(EAOPs)中阴极的氧化效率,通过液相沉淀法合成了锰氧化物/纳米石墨(MnOx /纳米-G)。研究了在不同温度(350、450和550摄氏度)下煅烧的MnOx /纳米G的结构和性能。结果表明,在550摄氏度时发生了纳米G灰化和MnOx附聚。事实证明,在450摄氏度下煅烧的MnOx /纳米G具有最高的苯酚降解效率。 MnOx / nano-G(450摄氏度)中的Mn价为+ 3(Mn2O3)和+4(MnO2)。通过评估H2O2和(OH)-O-中心点产率,酚与清除剂的降解,研究了制备的MnOx /纳米-G / 2-乙基蒽醌/活性炭(MnOx /纳米-G / 2-EAQ / AC)阴极的活性。和阻抗。 2-EAQ和MnOx分别可以促进O-2(H2O2)的双电子还原和(OH)-O-中心点自由基的产生。电解6小时后,抗​​生素制药废水的生物降解性(BOD5 / COD)从0.01提高到0.31,表明MnOx / nano-G / 2-EAQ / AC阴极有望进一步应用。 (C)2016 Elsevier Ltd.保留所有权利。

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