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碳酸氢钠增强 Mn(II)/过氧乙酸工艺高效降解新兴污染物:Mn(V)的形成与贡献。

Highly Efficient Degradation of Emerging Contaminants with Sodium Bicarbonate-Enhanced Mn(II)/Peracetic Acid Process: Formation and Contribution of Mn(V).

机构信息

Xiamen Key Laboratory of Municipal and Industrial Solid Waste Utilization and Pollution Control, College of Civil Engineering, Huaqiao University, Xiamen, Fujian 361021, P. R. China.

Department of Environmental Science & Engineering, Fudan University, Shanghai 200438, P. R. China.

出版信息

Environ Sci Technol. 2024 Nov 12;58(45):20313-20326. doi: 10.1021/acs.est.4c06878. Epub 2024 Nov 3.

DOI:10.1021/acs.est.4c06878
Abstract

Organic ligands have been extensively used to enhance the catalytic performance of manganese ion (Mn(II)) for peracetic acid (PAA). In this study, sodium bicarbonate (NaHCO), an economical and eco-friendly inorganic ligand, was introduced to enhance the degradation of emerging contaminants (ECs) in the Mn(II)/PAA process. NaHCO could significantly improve the oxidizing ability of the Mn(II)/PAA process over the initial pH range of 3.0-11.0. Mn(V) was identified as the primary reactive species for degrading naproxen in the NaHCO/Mn(II)/PAA process. HCO could complex with Mn(II) to generate Mn(II)-HCO, which has a lower redox potential to enhance the catalytic activity of Mn(II). Mn(II)-HCO reacted with PAA to produce Mn(III)-HCO and CHC(O)O. Mn(V)-HCO was generated via two-electron transfer between Mn(III)-HCO and PAA. Although organic radicals were detected in the NaHCO/Mn(II)/PAA process, naproxen was mainly degraded by Mn(V)-HCO via one-electron transfer along with the formation of MnO. Notably, the coexisting hydrogen peroxide was vital in the reduction of MnO to Mn(II/III), thereby enhancing the continuous generation of Mn(V)-HCO. NaHCO/Mn(II)/PAA process exhibited exceptional oxidation performance in actual water samples. This study proposed a strategy utilizing an eco-friendly inorganic ligand to address the inherent drawbacks of organic ligand-enhanced Mn(II)/PAA processes and highlighted its potential applications in the removal of ECs.

摘要

有机配体被广泛用于增强锰离子(Mn(II))对过氧乙酸(PAA)的催化性能。在这项研究中,碳酸氢钠(NaHCO),一种经济且环保的无机配体,被引入以增强 Mn(II)/PAA 过程中新兴污染物(ECs)的降解。NaHCO 可以显著提高 Mn(II)/PAA 过程在初始 pH 值 3.0-11.0 范围内的氧化能力。Mn(V)被确定为 NaHCO/Mn(II)/PAA 过程中降解萘普生的主要反应性物质。HCO 可以与 Mn(II)配合生成 Mn(II)-HCO,其还原电位较低,从而增强 Mn(II)的催化活性。Mn(II)-HCO 与 PAA 反应生成 Mn(III)-HCO 和 CHC(O)O。Mn(V)-HCO 通过 Mn(III)-HCO 和 PAA 之间的两电子转移生成。尽管在 NaHCO/Mn(II)/PAA 过程中检测到有机自由基,但萘普生主要通过 Mn(V)-HCO 进行单电子转移降解,同时形成 MnO。值得注意的是,共存的过氧化氢在将 MnO 还原为 Mn(II/III)方面至关重要,从而增强了 Mn(V)-HCO 的连续生成。NaHCO/Mn(II)/PAA 过程在实际水样中表现出出色的氧化性能。本研究提出了一种利用环保无机配体的策略来解决有机配体增强 Mn(II)/PAA 过程中的固有缺陷,并强调了其在去除 ECs 方面的潜在应用。

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