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通过配合的 Mn(II)增强过一硫酸盐活化:一种涉及锰中间体的新型非自由基氧化机制。

Enhanced peroxymonosulfate activation via complexed Mn(II): A novel non-radical oxidation mechanism involving manganese intermediates.

机构信息

Key Laboratory for City Cluster Environmental Safety and Green Development of the Ministry of Education, Institute of Environmental and Ecological Engineering, Guangdong University of Technology, Guangzhou 510006, China; Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Guangzhou 511458, China.

Key Laboratory of Songliao Aquatic Environment, Ministry of Education, School of Municipal and Environmental Engineering, Jilin Jianzhu University, Changchun 130118, China.

出版信息

Water Res. 2021 Apr 1;193:116856. doi: 10.1016/j.watres.2021.116856. Epub 2021 Jan 19.

Abstract

In recent years, the activation of persulfates (peroxydisulfate (PDS) and peroxymonosulfate (PMS)) via transition metal ions for contaminants degradation has received extensive attention in water treatment. There has been growing interest on the mechanism (radical versus non-radical pathway) of activation processes. Interestingly, in contrast to copper, iron or cobalt ions regarded as effective activators for persulfates, manganese ion (Mn(II)) is inefficient for persulfates activation. Inspired by the enhanced stability of manganese species by ligands, this study for the first time systematically investigated the Mn(II)/persulfates with different ligands as a novel oxidation technology. UV-vis spectrometry, chemical probing method and mass spectrometry were used to explore the reactive intermediate (free radical versus high-valent manganese species) therein. It was surprisingly found that the oxidation efficiency of Mn(II)/ligand/persulfates system was highly dependent on the nature of persulfates and ligands. Mn(II) chelated by amino ligands such as ethylenediaminetetraacetic acid (EDTA) and nitrilotriacetate (NTA) could efficiently trigger the oxidation of contaminants (e.g., recalcitrant compounds nitrophenol, benzoic acid and atrazine) by PMS, suggesting a promising Mn(II)/ligand/PMS technology for environmental decontamination especially under manganese-rich conditions. High-valent Mn species (Mn(V)) but not free radicals was demonstrated to be the dominant reactive intermediate, where Mn(III) species played a vital role in Mn(V) generation. The formation of Mn(III) species was found to be affected by the reactivity of persulfates and the type of ligands, thus influencing its further oxidation to Mn(V) species. This study presents a new oxidation process based on the combination of PMS and Mn(II) complex and broadens the knowledge of persulfates activation as well as manganese chemistry for decontamination in water treatment.

摘要

近年来,通过过渡金属离子激活过硫酸盐(过二硫酸盐(PDS)和过一硫酸盐(PMS))来降解污染物在水处理中受到了广泛关注。人们对其激活过程的机制(自由基途径与非自由基途径)越来越感兴趣。有趣的是,与被认为是过硫酸盐有效激活剂的铜、铁或钴离子不同,锰离子(Mn(II))对过硫酸盐的激活效率较低。受配体增强锰物种稳定性的启发,本研究首次系统地研究了不同配体的 Mn(II)/过硫酸盐作为一种新型氧化技术。使用紫外可见光谱法、化学探测法和质谱法来探究其中的反应中间体(自由基与高价锰物种)。令人惊讶的是,发现 Mn(II)/配体/过硫酸盐体系的氧化效率高度依赖于过硫酸盐和配体的性质。Mn(II)与乙二胺四乙酸(EDTA)和氮三乙酸(NTA)等氨基配体螯合,可以有效地引发 PMS 对污染物(如难降解化合物硝基酚、苯甲酸和莠去津)的氧化,这表明 Mn(II)/配体/PMS 技术在环境去污方面具有广阔的应用前景,特别是在富锰条件下。实验证明,高价锰物种(Mn(V))而非自由基是主要的反应中间体,其中 Mn(III)物种在 Mn(V)的生成中起着至关重要的作用。发现 Mn(III)物种的形成受到过硫酸盐的反应活性和配体类型的影响,从而影响其进一步氧化为 Mn(V)物种。本研究提出了一种基于 PMS 和 Mn(II)配合物结合的新氧化过程,拓宽了过硫酸盐激活以及锰化学在水处理中用于去污的知识。

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