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过氧单硫酸盐对二氯乙腈和三氯乙腈消毒副产物的亲核水解:动力学与机理

Nucleophilic hydrolysis of dichloroacetonitrile and trichloroacetonitrile disinfection byproducts by peroxymonosulfate: Kinetics and mechanisms.

作者信息

Yu Yangyi, Li Juan, Zhou Junhui, Cao Ying, Guo Qin, Liu Yongze, Yang Yi, Jiang Jin

机构信息

Key Laboratory for City Cluster Environmental Safety and Green Development of the Ministry of Education, School of Ecology, Environment, and Resources, Guangdong University of Technology, Guangzhou 510006, China.

Advanced Interdisciplinary Institute of Environment and Ecology, Guangdong Provincial Key Laboratory of Wastewater Information Analysis and Early Warning, Beijing Normal University, Zhuhai 519087, China.

出版信息

Chemosphere. 2024 Sep;363:142875. doi: 10.1016/j.chemosphere.2024.142875. Epub 2024 Jul 15.

Abstract

In this work, it was found that peroxymonosulfate (PMS) could appreciably accelerate the transformation rates of dichloroacetonitrile (DCAN) and trichloracetonitrile (TCAN) in aqueous solutions, especially under alkaline pHs. The impact of reactive oxygen species scavengers (methyl alcohol for sulfate radical, tert-butyl alcohol for hydroxyl radical, and azide for singlet oxygen) and water matrices (chloride (Cl), bicarbonate (HCO), and natural organic matter (NOM)) on DCAN and TCAN transformation by PMS is evaluated, revealing negligible effects. A nucleophilic hydrolysis pathway, as opposed to an oxidation process, was proposed for the transformation of DCAN and TCAN by PMS, supported by the hydrolyzable characteristics of these compounds and validated through density functional theory calculations. Kinetic analysis indicated that the transformation of DCAN and TCAN by PMS adhered to a second-order kinetic law, with higher reaction rates observed at elevated pH levels within the range of 7.0-10.0. Kinetic modeling incorporating the hydrolytic contributions of water, hydroxyl ion, and protonated and deprotonated PMS (i.e., HSO and SO) effectively fitted the experimental data. Species-specific second-order rate constants reveal that SO exhibited significantly higher reactivity towards DCAN ((1.69 ± 0.22) × 10 Mh) and TCAN ((6.06 ± 0.18) × 10 Mh) compared to HSO ((2.14 ± 0.12) × 10 Mh) for DCAN; and (1.378 ± 0.11) × 10 Mh for TCAN). Comparative analysis of DCAN and TCAN transformation efficiencies by four different oxidants indicated that PMS rivaled chlorine but falls short of hydrogen peroxide, with peroxydisulfate displaying negligible reactivity. Overall, this study uncovers the nucleophilic hydrolysis characteristics of PMS, supplementing its recognized role as an oxidant precursor or mild oxidant, and underscores its significant implications for environmental remediation.

摘要

在本研究中发现,过氧单硫酸盐(PMS)能够显著加快二氯乙腈(DCAN)和三氯乙腈(TCAN)在水溶液中的转化速率,尤其是在碱性pH条件下。评估了活性氧清除剂(甲醇用于清除硫酸根自由基、叔丁醇用于清除羟基自由基、叠氮化物用于清除单线态氧)和水基质(氯离子(Cl)、碳酸氢根(HCO)和天然有机物(NOM))对PMS介导的DCAN和TCAN转化的影响,结果显示影响可忽略不计。与氧化过程不同,提出了一条亲核水解途径用于解释PMS对DCAN和TCAN的转化,这些化合物的可水解特性支持了该途径,并通过密度泛函理论计算得到验证。动力学分析表明,PMS对DCAN和TCAN的转化遵循二级动力学规律,在7.0 - 10.0范围内,pH升高时反应速率更高。纳入水、氢氧根离子以及质子化和去质子化的PMS(即HSO和SO)水解贡献的动力学模型有效地拟合了实验数据。物种特异性二级反应速率常数表明,与HSO相比,SO对DCAN((1.69 ± 0.22) × 10 Mh)和TCAN((6.06 ± 0.18) × 10 Mh)的反应活性显著更高;对于DCAN,HSO的二级反应速率常数为(2.14 ± 0.12) × 10 Mh;对于TCAN,为(1.378 ± 0.11) × 10 Mh)。对四种不同氧化剂介导的DCAN和TCAN转化效率的比较分析表明,PMS与氯相当,但不及过氧化氢,过二硫酸盐的反应活性可忽略不计。总体而言,本研究揭示了PMS的亲核水解特性,补充了其作为氧化剂前体或温和氧化剂的已知作用,并强调了其对环境修复的重要意义。

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