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在钴(II)/过氧乙酸体系中,意外的副反应主导了芳香胺的氧化转化。

Unexpected side reactions dominate the oxidative transformation of aromatic amines in the Co(II)/peracetic acid system.

作者信息

Wu Jing-Hang, Yang Tian-Hao, Chen Fei, Yu Han-Qing

机构信息

Department of Environmental Science and Engineering, CAS Key Laboratory of Urban Pollutant Conversion, University of Science and Technology of China, Hefei 230026, China.

出版信息

PNAS Nexus. 2024 Jan 30;3(2):pgae040. doi: 10.1093/pnasnexus/pgae040. eCollection 2024 Feb.

Abstract

Aromatic amines (AAs), ubiquitous in industrial applications, pose significant environmental hazards due to their resistance to conventional wastewater treatments. Peracetic acid (PAA)-based advanced oxidation processes (AOPs) have been proposed as effective strategies for addressing persistent AA contaminants. While the organic radicals generated in these systems are believed to be selective and highly oxidative, acetate residue complicates the evaluation of AA removal efficiency. In this work, we explored transformation pathways of AAs in a representative Co(II)-catalyzed PAA system, revealing five side reactions (i.e. nitrosation, nitration, coupling, dimerization, and acetylation) that yield 17 predominantly stable and toxic by-products. The dominant reactive species was demonstrated as Co-OOC(O)CH, which hardly facilitated ring-opening reactions. Our findings highlight the potential risks associated with PAA-based AOPs for AA degradation and provide insights into selecting suitable catalytic systems aimed at efficient and by-product-free degradation of pollutants containing aromatic -NH.

摘要

芳香胺(AAs)在工业应用中普遍存在,由于其对传统废水处理具有抗性,因而对环境构成重大危害。基于过氧乙酸(PAA)的高级氧化工艺(AOPs)已被提议作为解决持久性AA污染物的有效策略。虽然这些体系中产生的有机自由基被认为具有选择性且氧化性很强,但乙酸盐残留物使评估AA去除效率变得复杂。在这项工作中,我们探索了AAs在典型的钴(II)催化PAA体系中的转化途径,揭示了五个副反应(即亚硝化、硝化、偶联、二聚化和乙酰化),这些反应产生了17种主要稳定且有毒的副产物。主要的活性物种被证明是Co - OOC(O)CH,它几乎不促进开环反应。我们的研究结果突出了基于PAA的AOPs降解AA所带来的潜在风险,并为选择合适的催化体系以实现含芳香 -NH污染物的高效且无副产物降解提供了见解。

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