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

过氧乙酸 降级(电信) 碳酸氢钠 化学 碳酸氢盐 污染 环境化学 无机化学 核化学 过氧化氢 生物化学 有机化学 计算机科学 生物 电信 生态学
作者
Linfeng He,Jing Zou,Jian‐Ying Wu,Sheng Li,Wu Zhi,Yixin Huang,修至 出口,Qingfeng Cheng,Panpan Wang,Jun Ma
出处
期刊:Environmental Science & Technology [American Chemical Society]
标识
DOI:10.1021/acs.est.4c06878
摘要

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 (NaHCO3), an economical and eco-friendly inorganic ligand, was introduced to enhance the degradation of emerging contaminants (ECs) in the Mn(II)/PAA process. NaHCO3 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 NaHCO3/Mn(II)/PAA process. HCO3– could complex with Mn(II) to generate Mn(II)-HCO3–, which has a lower redox potential to enhance the catalytic activity of Mn(II). Mn(II)-HCO3– reacted with PAA to produce Mn(III)-HCO3– and CH3C(O)O•. Mn(V)-HCO3– was generated via two-electron transfer between Mn(III)-HCO3– and PAA. Although organic radicals were detected in the NaHCO3/Mn(II)/PAA process, naproxen was mainly degraded by Mn(V)-HCO3– via one-electron transfer along with the formation of MnO2. Notably, the coexisting hydrogen peroxide was vital in the reduction of MnO2 to Mn(II/III), thereby enhancing the continuous generation of Mn(V)-HCO3–. NaHCO3/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.
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