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Degradation of sulfamethoxazole by UV, UV/H2O2 and UV/persulfate (PDS): Formation of oxidation products and effect of bicarbonate

机译:UV,UV / H2O2和UV /过硫酸盐(PDS)降解磺胺甲恶唑:氧化产物的形成和碳酸氢盐的影响

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摘要

The frequent detection of sulfamethoxazole (SMX) in wastewater and surface waters gives rise of concerns about their ecotoxicological, effects and potential risks to induce antibacterial resistant genes. UV/hydrogen peroxide (UV/H2O2) and UV/persulfate (UV/PDS) advanced oxidation processes have been demonstrated to be effective for the elimination of SMX, but there is still a need for a deeper understanding of product formations. In this study, we identified and compared the transformation products of SMX in UV, UV/H2O2 and UV/PDS processes. Because of the electrophilic nature of SO4 center dot-, the second-order rate constant for the reaction of sulfate radical (SO4 center dot-) with the anionic form of SMX was higher than that with the neutral form, while hydroxyl radical (center dot OH) exhibited comparable reactivity to both forms. The direct photolysis of SMX predominately occurred through cleavage of the N-S bond, rearrangement of the isoxazole ring, and hydroxylation mechanisms. Hydroxylation was the dominant pathway for the reaction of center dot OH with SMX. SO4 center dot- favored attack on -NH2 group of SMX to generate a nitro derivative and dimeric products. The presence of bicarbonate in UV/H2O2 inhibited the formation of hydroxylated products, but promoted the formation of the nitro derivative and the dimeric products. In UV/PDS, bicarbonate increased the formation of the nitro derivative and the dimeric products, but decreased the formation of the hydroxylated dimeric products. The different effect of bicarbonate on transformation products in UV/H2O2 vs. UV/PDS suggested that carbonate radical (CO3 center dot-) oxidized SMX through the electron transfer mechanism similar to SO4 center dot- but with less oxidation capacity. Additionally, SO4 center dot- and CO3 center dot- exhibited higher reactivity to the oxazole ring than the isoxazole ring of SMX. Ecotoxicity of transformation products was estimated by ECOSAR program based on the quantitative structure-activity relationship analysis as well as by experiments using Vibrio fischeri, and these results indicated that the oxidation of SO4 center dot- or CO3 center dot- with SMX generated more toxic products than those of (OH)-O-center dot. (C) 2017 Elsevier Ltd. All rights reserved.
机译:废水和地表水中的磺胺甲恶唑(SMX)的频繁检测引起人们对它们的生态毒理学,影响以及诱导抗菌素耐药基因的潜在风险的关注。 UV /过氧化氢(UV / H2O2)和UV /过硫酸盐(UV / PDS)先进的氧化工艺已被证明可有效消除SMX,但仍需要对产品形成有更深入的了解。在这项研究中,我们确定并比较了SMX在UV,UV / H2O2和UV / PDS工艺中的转化产物。由于SO4中心点的亲电性质,硫酸根(SO4中心点)与SMX阴离子形式的反应的二级速率常数高于中性形式,而羟基自由基(中心点)的反应速率常数高OH)对这两种形式均表现出相当的反应性。 SMX的直接光解主要通过N-S键的断裂,异恶唑环的重排和羟基化机制发生。羟基化是中心点OH与SMX反应的主要途径。 SO4中心点有利于攻击SMX的-NH2基团,生成硝基衍生物和二聚体产物。 UV / H2O2中碳酸氢盐的存在抑制了羟基化产物的形成,但促进了硝基衍生物和二聚产物的形成。在UV / PDS中,碳酸氢盐增加了硝基衍生物和二聚体产物的形成,但减少了羟基化的二聚体产物的形成。碳酸氢盐对UV / H2O2与UV / PDS转化产物的不同影响表明,碳酸盐自由基(CO3中心点)通过类似于SO4中心点的电子转移机理氧化了SMX,但氧化能力较低。此外,SO4中心点和CO3中心点对恶唑环的反应性均高于SMX的异恶唑环。通过ECOSAR程序,基于定量构效关系分析以及费氏弧菌的实验,估算了转化产物的生态毒性,这些结果表明,SMX对SO4中心点或CO3中心点的氧化产生了更多的毒性产物。比(OH)-O-中心点的(C)2017 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Water Research》 |2017年第1期|196-207|共12页
  • 作者单位

    Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China;

    Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China;

    Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China;

    Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China;

    Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China;

    Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China;

    Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China;

    Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China;

    Harbin Univ Sci & Technol, Coll Chem & Environm Engn, Key Lab Green Chem Engn & Technol Coll Heilongjia, Harbin 150040, Heilongjiang, Peoples R China;

    Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China;

    Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Sulfamethoxazole; Hydroxyl radical; Sulfate radical; Carbonate radical; Transformation products;

    机译:磺胺甲恶唑;羟基自由基;硫酸根自由基;碳酸根自由基;转化产物;

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