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通过电化学生成的过氧化氢和原子氢反应产生羟基自由基:一种有效的污染物氧化过程?

Hydroxyl Radical Production via a Reaction of Electrochemically Generated Hydrogen Peroxide and Atomic Hydrogen: An Effective Process for Contaminant Oxidation?

机构信息

UNSW Centre for Transformational Environmental Technologies (CTET), Yixing, Jiangsu 214206, P. R. China.

School of Civil and Environmental Engineering, UNSW Sydney, Sydney, NSW 2052, Australia.

出版信息

Environ Sci Technol. 2022 May 3;56(9):5820-5829. doi: 10.1021/acs.est.2c00405. Epub 2022 Apr 20.

DOI:10.1021/acs.est.2c00405
PMID:35442646
Abstract

An electrochemical advanced oxidation process (EAOP) is demonstrated with a catalytic cathode capable of simultaneously catalyzing the hydrogen evolution reaction (HER) and the oxygen reduction reaction (ORR) with resultant in situ generation of atomic hydrogen (H*) and hydrogen peroxide (HO). A palladium-coated carbon-PTFE gas diffusion electrode (Pd/C GDE) was used as a catalytic cathode with hydroxyl radical (OH) formed as a result of the reaction of electrogenerated H* with HO. As both the HER and ORR can be induced to occur at the same cathode, the H*/GDE process results in more effective degradation of organic contaminants than can be achieved by a conventional H*/HO process involving direct addition of HO. At circumneutral pH, 82.7% of added formate was degraded after 2 h treatment at an applied potential of -1.0 V vs Ag/AgCl with relatively low concentrations of generated HO remaining in the solution. We also show that H* and HO (and thus OH) can be electrogenerated effectively over a wide range of pH (3.2-7.0). These results suggest that by in situ generation of H* and HO, the H*/GDE process is able to produce significant amounts of OH without external chemical addition and thus offers an alternative method for abatement of aqueous organic contaminants.

摘要

电化学高级氧化工艺(EAOP)通过一种催化阴极得以实现,该阴极能够同时催化析氢反应(HER)和氧还原反应(ORR),从而原位生成原子氢(H*)和过氧化氢(HO)。使用涂有钯的碳-PTFE 气体扩散电极(Pd/C GDE)作为催化阴极,由于电生成的 H与 HO 反应而形成羟基自由基(OH)。由于 HER 和 ORR 都可以在同一阴极上引发,因此 H/GDE 工艺导致有机污染物的降解比涉及直接添加 HO 的传统 H*/HO 工艺更有效。在中性 pH 下,在施加的-1.0 V 相对于 Ag/AgCl 的电位下处理 2 小时后,添加的甲酸盐中有 82.7%被降解,溶液中剩余的生成的 HO 浓度相对较低。我们还表明,H和 HO(因此 OH)可以在很宽的 pH 范围内(3.2-7.0)有效地电生成。这些结果表明,通过原位生成 H和 HO,H*/GDE 工艺能够在无需外部化学添加的情况下产生大量 OH,从而为消除水中有机污染物提供了一种替代方法。

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