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