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缺陷富里界面 Mo/MoO 的简便合成用于高效过一硫酸盐活化和难降解污染物降解。

Facile synthesis of defect-rich interfacial Mo/MoO for efficient peroxymonosulfate activation and refractory pollutants degradation.

机构信息

Key Laboratory of Mesoscopic Chemistry, MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China.

Key Laboratory of Mesoscopic Chemistry, MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China.

出版信息

Environ Pollut. 2024 Nov 15;361:124788. doi: 10.1016/j.envpol.2024.124788. Epub 2024 Aug 20.

DOI:10.1016/j.envpol.2024.124788
PMID:39173860
Abstract

Peroxymonosulfate-based advanced oxidation process (PMS-AOP) has shown great potential in sewage purification, and catalyst development capable of efficient PMS activation is a key while challenging element. Herein we reported a facile electro-explosive route to synthesize the oxygen vacancy (Vo)-enriched Mo/MoO without using chemical reagents. The detailed studies suggested that the synergy of Mo active site and Vo in the catalyst significantly boosted the activation kinetics of PMS. Evidently, the Mo site of different oxidation states contributed to chemical activation of PMS, while the Vo favored the activation of PMS and the generation of non-radical O species. As a result, the Mo/MoO-10 h/PMS system delivered a complete removal of acid orange 7 (AO7) within 4 min, significantly exceeding the activity of Mo/PMS (16%), MoO-H/PMS (25%) and most of other PMS-based systems. Moreover, the current system showed high potential for removal of different pollutants including antibiotics and organic dyes. Radical quenching experiments and electron paramagnetic resonance (EPR) studies revealed that the O species was significant for AO7 decomposition. This work provided a novel strategy to a batch-scale synthesis of high-performance PMS activator for water remediation in practice.

摘要

基于过一硫酸盐的高级氧化工艺(PMS-AOP)在污水净化方面显示出巨大的潜力,而能够高效激活 PMS 的催化剂的开发是关键也是具有挑战性的因素。本文报道了一种简便的电爆炸方法,无需使用化学试剂即可合成富含氧空位(Vo)的 Mo/MoO。详细研究表明,催化剂中 Mo 活性位和 Vo 的协同作用显著提高了 PMS 的活化动力学。显然,不同氧化态的 Mo 位有助于 PMS 的化学活化,而 Vo 有利于 PMS 的活化和非自由基 O 物种的生成。因此,Mo/MoO-10 h/PMS 体系在 4 min 内可完全去除酸性橙 7(AO7),其活性明显超过 Mo/PMS(16%)、MoO-H/PMS(25%)和大多数其他基于 PMS 的体系。此外,该体系对去除不同污染物(包括抗生素和有机染料)具有很高的潜力。自由基猝灭实验和电子顺磁共振(EPR)研究表明,O 物种对 AO7 的分解很重要。这项工作为实际水修复中高性能 PMS 活化剂的批量化合成提供了一种新策略。

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