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掺硼金刚石用于羟自由基和硫酸根自由基的电生成、转化及无电压可持续氧化。

Boron-Doped Diamond for Hydroxyl Radical and Sulfate Radical Anion Electrogeneration, Transformation, and Voltage-Free Sustainable Oxidation.

机构信息

School of Chemical Science and Engineering, Shanghai Key Lab of Chemical Assessment and Sustainability, Tongji University, Shanghai, 200092, P. R. China.

Shanghai Key Laboratory of Materials Protection and Advanced Materials in Electric Power, Shanghai University of Electric Power, Shanghai, 200090, P. R. China.

出版信息

Small. 2019 Nov;15(48):e1900153. doi: 10.1002/smll.201900153. Epub 2019 Mar 8.

Abstract

Boron-doped diamond-based electrochemical advanced oxidation processes (BDD-EAOPs) have attracted much attention. However, few systematic studies concerning the radical mechanism in BDD-EAOPs have been published. In situ electron paramagnetic resonance spectrometry is used to confirm that SO is directly electrogenerated from SO . Then, excess SO dimerizes to form S O and accumulates in the BDD-EAOP system. But no S O accumulates at pH = 10 owing to the rapid transformation of SO and S O . Above the overpotential of water oxidation, OH is electrogenerated and cooperated with SO . In the power-off phase, the accumulated S O can be reactivated to SO via specific degradation intermediates to achieve sustainable degradation. Di-n-butyl phthalate (DnBP), a typical endocrine disruptor, is selected as a model contaminant. Surprisingly, 99.8% of DnBP (initial concentration of 1 mg L ) is removed, using an intermittent power supply strategy with a periodic 10 min power-on phase at a duty ratio of 1:2, reducing the electrical energy consumption (1.8 kWh m ) by more than 30% compared with continuous power supply consumption. These radical electrogeneration transformation mechanisms reveal an important new strategy for sustainable oxidation, especially for in situ water restoration, and are expected to provide a theoretical basis for BDD applications.

摘要

基于硼掺杂金刚石的电化学高级氧化工艺(BDD-EAOPs)受到了广泛关注。然而,关于 BDD-EAOPs 中自由基机制的系统研究却很少见诸报道。本研究采用现场电子顺磁共振波谱技术证实了 SO 是直接由 SO 4 2-电化学生成的。然后,过量的 SO 2 二聚化形成 S 2 O 3 2-并在 BDD-EAOP 体系中积累。但是在 pH = 10 时由于 SO 2 和 S 2 O 3 2-的快速转化,没有 S 2 O 3 2-积累。在超过水氧化的过电位后, OH 被电化学生成并与 SO 2 结合。在关断阶段,通过特定的降解中间产物可以将积累的 S 2 O 3 2-重新激活为 SO 2 ,从而实现可持续降解。邻苯二甲酸二丁酯(DnBP)作为一种典型的内分泌干扰物,被选为模型污染物。令人惊讶的是,采用间歇供电策略,以 1:2 的占空比周期性地开启 10 min(周期时间为 10 min),与连续供电相比,电能消耗(1.8 kWh m )降低了 30%以上,即可去除 99.8%的初始浓度为 1 mg L 的 DnBP。这些自由基电生成转化机制揭示了一种可持续氧化的重要新策略,特别是对于原位水修复,有望为 BDD 的应用提供理论基础。

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