电合成
聚苯胺
过氧化氢
蒽醌
化学
化学工程
聚吡咯
电化学
电催化剂
材料科学
有机化学
电极
聚合
聚合物
工程类
物理化学
作者
Qianhong Zhu,Marlena Hinkle,David J. Kim,Jae‐Hong Kim
标识
DOI:10.1021/acsestengg.0c00173
摘要
Advanced oxidation processes (AOPs) target the chemical destruction of a wide range of nonbiodegradable, toxic, and recalcitrant organic pollutants instead of removal via physical separation, which produces contaminant-laden concentrates or solids. Hydrogen peroxide (H 2 O 2 ) is the most widely used precursor that produces a highly reactive and nonselective hydroxyl radical at the site of an AOP through activation by UV irradiation. The potential for AOPs to meet the growing demand of transforming a centralized treatment and distribution practice into a modular, small-scale, and decentralized treatment paradigm can be maximized by innovative technologies that can synthesize precursor chemicals also at the site of water treatment, eliminating the need for a continuous chemical supply. We here present an electrochemical H 2 O 2 generation cell that produces a large quantity of H 2 O 2 while consuming only 0.2 to 20% of the total electricity consumption of AOPs in various AOP application scenarios employing UV activation. We achieve high electrochemical H 2 O 2 production efficiency by synthesizing an anthraquinone-modified polyaniline composite that enables an efficient two-electron oxygen reduction reaction. Polyaniline functions as a conductive support with abundant attachment sites, and anthraquinone ensures selective H 2 O 2 generation. In a flow cell equipped with a gas diffusion cathode, H 2 O 2 can be produced at a rate of 1.80 mol g catalyst –1 hr –1 at 100 mA with a Faradaic efficiency of 95.83%. Finally, we examined the H 2 O 2 production capability of the device with simulated drinking water and wastewater as feed electrolytes to demonstrate its potential for real-world operation scenarios.
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