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通过微弧氧化法制备 ZnSnO@Ti 陶瓷膜阳极用于 2e WOR 降解不对称二甲肼(UDMH)。

ZnSnO@Ti ceramic film anode preparation by microarc oxidation for 2e WOR degradation of unsymmetrical dimethylhydrazine (UDMH).

机构信息

School of Light Industry and Chemical Engineering, Dalian Polytechnic University, No. 1 Qinggongyuan, Ganjinzi District, Dalian, 116034, PR China.

College of Marine Science-Technology and Environment, Dalian Ocean University, No. 52 Heishijiao, Shahekou District, Dalian, 116023, PR China.

出版信息

J Environ Manage. 2024 Apr;356:120724. doi: 10.1016/j.jenvman.2024.120724. Epub 2024 Mar 24.

DOI:10.1016/j.jenvman.2024.120724
PMID:38527385
Abstract

The main challenge facing the anodic electro-Fenton through the 2e water oxidation reaction (WOR) for toxics degradation lies in the electrode's stability, because the anodic oxygen evolution (OER) generated O will inevitably exfoliate the electro-active components loaded on the electrode substrate. To address this point, two aspects need attention: 1) Identifying a catalyst that exhibits both excellent electrocatalytic activity and selectivity can improve the faradaic efficiency of hydrogen peroxide (HO); 2) Employing novel methods for fabricating highly stable electrodes, where active sites can be firmly coated. Consequently, this study utilized microarc oxidation (MAO) to prepare a ceramic film electrode ZnSnO@Ti at 300 V. ZnSnO acts as an WOR electrocatalyst and further improved the generation of HO for treating real wastewater containing Unsymmetrical Dimethylhydrazine (UDMH). From the perspective of characterization of electrode structure, ZnSnO@Ti forms a stable active coating, the electrochemical yield of HO is high up to 78.4 μmol h cm, and the selectivity of HO is over 80% at 3.3 V vs. RHE, which can be fully applied to scenarios where it is inconvenient to transport HO and need in-situ safe production. Additionally, the prepared electrodes exhibit significant stability, suitable for various applications, providing insightful preparation strategies and experiences for constructing highly stable anodes.

摘要

阳极电芬顿通过 2e 水氧化反应 (WOR) 进行毒物降解所面临的主要挑战在于电极的稳定性,因为阳极氧气的产生 (OER) 会不可避免地剥离负载在电极基底上的电活性组件。为了解决这一点,需要注意两个方面:1) 找到一种同时具有优异电催化活性和选择性的催化剂,可以提高过氧化氢(HO)的法拉第效率;2) 采用新型方法制备高度稳定的电极,其中活性位点可以被牢固地覆盖。因此,本研究利用微弧氧化 (MAO) 在 300 V 下制备了陶瓷膜电极 ZnSnO@Ti。ZnSnO 作为 WOR 电催化剂,进一步提高了 HO 的生成,用于处理含有偏二甲基肼(UDMH)的实际废水。从电极结构的表征角度来看,ZnSnO@Ti 形成了稳定的活性涂层,HO 的电化学产率高达 78.4 μmol h cm,在 3.3 V vs. RHE 时 HO 的选择性超过 80%,可完全应用于不方便运输 HO 且需要原位安全生产的场景。此外,所制备的电极表现出显著的稳定性,适用于各种应用,为构建高度稳定的阳极提供了有价值的制备策略和经验。

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