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用于高效活化过一硫酸盐的非晶态铁掺杂碳酸锰:降解橙黄 II 的机制与性能

Amorphous Fe-Doped Manganese Carbonate for Efficient Activation of Peroxymonosulfate: Mechanism and Performance Toward Orange II Degradation.

作者信息

Cheng Peng, Li Yuqing, Ma Yunlong, Qiu Cui, Fu Tengfei, Wang Yajie, Wu Feng

机构信息

Hubei Key Laboratory of Biomass Resource Chemistry and Environmental Biotechnology, School of Resources and Environmental Science, Wuhan University, Wuhan 430079, China.

Institut de Chimie de Clermont Ferrand (ICCF) UMR 6296, Université Clermont Auvergne, Centre National de la Recherche Scientifique (CNRS), Clermont Auvergne INP, BP 80026, F-63171 Clermont-Ferrand, France.

出版信息

Molecules. 2025 May 26;30(11):2325. doi: 10.3390/molecules30112325.

Abstract

A novel amorphous Fe-doped manganese carbonate (a-FeMn-1) was synthesized via a facile co-precipitation method and evaluated as an efficient heterogeneous catalyst for the activation of peroxymonosulfate (PMS) in the degradation of Orange II. Among various Fe/Mn molar ratios, the 1:1 composition (a-FeMn-1) showed optimal catalytic activity, achieving 98% removal efficiency within 60 min under near-neutral pH conditions. Characterization results indicated that Fe doping effectively induced an amorphous structure and increased surface area and oxygen defects, promoting PMS activation. The system displayed broad pH applicability and resistance to Cl and natural organic matter, while degradation was inhibited by HCO and PO. EPR and quenching experiments confirmed that surface-bound sulfate radicals (SO), hydroxyl radicals (OH), and singlet oxygen (O) were the primary reactive species. XPS analysis further revealed the redox cycling of Fe and Mn and the involvement of defect oxygen in the PMS activation process. The catalyst also demonstrated excellent reusability over five cycles without significant loss in efficiency. This work provides insights into the rational design of amorphous bimetallic materials for sulfate radical-based advanced oxidation processes.

摘要

通过简便的共沉淀法合成了一种新型非晶态铁掺杂碳酸锰(a-FeMn-1),并将其作为一种高效的非均相催化剂用于活化过一硫酸盐(PMS)以降解橙黄II。在各种铁/锰摩尔比中,1:1组成(a-FeMn-1)表现出最佳催化活性,在近中性pH条件下60分钟内实现了98%的去除效率。表征结果表明,铁掺杂有效地诱导了非晶态结构,增加了表面积和氧缺陷,促进了PMS的活化。该体系显示出广泛的pH适用性以及对Cl和天然有机物的抗性,而HCO和PO会抑制降解。电子顺磁共振(EPR)和猝灭实验证实,表面结合的硫酸根自由基(SO)、羟基自由基(OH)和单线态氧(O)是主要的活性物种。X射线光电子能谱(XPS)分析进一步揭示了铁和锰的氧化还原循环以及缺陷氧在PMS活化过程中的作用。该催化剂在五个循环中还表现出优异的可重复使用性,效率没有明显损失。这项工作为基于硫酸根自由基的高级氧化过程中无定形双金属材料的合理设计提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a14/12155956/e63cabd6f5ef/molecules-30-02325-g001.jpg

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