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Photodegradation of sulfasalazine and its human metabolites in water by UV and UV/peroxydisulfate processes

机译:UV和UV /过氧化二硫酸盐光降解柳氮磺胺吡啶及其人体代谢物

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摘要

The widespread occurrence of pharmaceuticals and their metabolites in natural waters has raised great concerns about their potential risks on human health and ecological systems. This study systematically investigates the degradation of sulfasalazine (SSZ) and its two human metabolites, sulfapyridine (SPD) and 5-aminosalicylic acid (5-ASA), by UV and UV/peroxydisulfate (UV/PDS) processes. Experimental results show that SPD and 5-ASA were readily degraded upon UV 254 nm direct photolysis, with quantum yields measured to be (8.6 +/- 0.8) x 10(-3) and (2.4 +/- 0.1) x 10(-2) mol Einstein(-1), respectively. Although SSZ was resistant to direct UV photolysis, it could be effectively removed by both UV/H2O2 and UV/PDS processes, with fluence-based pseudo-first-order rate constants determined to be 0.0030 and 0.0038 cm(2) mJ(-1), respectively. Second-order rate constant between SO4 center dot- and SSZ was measured as (1.33 +/- 0.01) x 10(9) M-1 s(-1) by competition kinetic method. A kinetic model was established for predicting the degradation rate of SSZ in the UV/PDS process. Increasing the dosage of PDS significantly enhanced the degradation of SSZ in the UV/PDS process, which can be well predicted by the developed kinetic model. Natural water constituents, such as natural organic matter (NOM) and bicarbonate (HCO3-), influenced the degradation of SSZ differently. The azo functional group of SSZ molecule was predicted as the reactive site susceptible to electrophilic attack by SO4 center dot- by frontier electron densities (FEDs) calculations. Four intermediate products arising from azo bond cleavage and SO2 extrusion were identified by solid phase extraction-liquid chromatography-triple quadrupole mass spectrometry (SPE-LC-MS/MS). Based on the products identified, detailed transformation pathways for SSZ degradation in the UV/PDS system were proposed. Results reveal that UV/PDS could be an efficient approach for remediation of water contaminated by SSZ and its metabolites. (C) 2018 Elsevier Ltd. All rights reserved.
机译:天然水域中药物及其代谢产物的广泛存在引起了人们对其潜在危害人类健康和生态系统的担忧。这项研究系统地研究了通过UV和UV /过氧二硫酸盐(UV / PDS)工艺降解柳氮磺吡啶(SSZ)及其两种人体代谢物磺胺吡啶(SPD)和5-氨基水杨酸(5-ASA)的过程。实验结果表明,SPD和5-ASA在254 nm UV直接光解后很容易降解,量子产率分别为(8.6 +/- 0.8)x 10(-3)和(2.4 +/- 0.1)x 10(- 2)分别是mol Einstein(-1)。尽管SSZ可以抵抗直接的UV光解,但可以通过UV / H2O2和UV / PDS工艺将其有效去除,基于注量的拟一级反应速率常数确定为0.0030和0.0038 cm(2)mJ(-1) ), 分别。 SO4中心点和SSZ之间的二阶速率常数通过竞争动力学方法测量为(1.33 +/- 0.01)x 10(9)M-1 s(-1)。建立了动力学模型以预测SS / Z在UV / PDS过程中的降解速率。增加PDS的剂量显着增强了UV / PDS过程中SSZ的降解,这可以通过开发的动力学模型很好地预测。天然水成分,例如天然有机物(NOM)和碳酸氢盐(HCO3-),对SSZ的降解有不同的影响。通过前沿电子密度(FED)计算,将SSZ分子的偶氮官能团预测为易受SO4中心点电性攻击的反应位点。通过固相萃取-液相色谱-三重四极杆质谱(SPE-LC-MS / MS)鉴定了偶氮键断裂和SO2挤出产生的四种中间产物。根据鉴定出的产物,提出了在UV / PDS系统中SSZ降解的详细转化途径。结果表明,UV / PDS可能是修复被SSZ及其代谢物污染的水的有效方法。 (C)2018 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Water Research》 |2018年第15期|299-309|共11页
  • 作者单位

    Nanjing Agr Univ, Coll Resources & Environm Sci, Nanjing 210095, Jiangsu, Peoples R China;

    Nanjing Agr Univ, Coll Resources & Environm Sci, Nanjing 210095, Jiangsu, Peoples R China;

    Univ Claude Bernard Lyon 1, Univ Lyon, CNRS, IRCELYON, F-69626 Villeurbanne, France;

    Nanjing Agr Univ, Coll Resources & Environm Sci, Nanjing 210095, Jiangsu, Peoples R China;

    Nanjing Agr Univ, Coll Resources & Environm Sci, Nanjing 210095, Jiangsu, Peoples R China;

    Univ Claude Bernard Lyon 1, Univ Lyon, CNRS, IRCELYON, F-69626 Villeurbanne, France;

    Univ Claude Bernard Lyon 1, Univ Lyon, CNRS, IRCELYON, F-69626 Villeurbanne, France;

  • 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

    Peroxydisulfate; Photolysis; Sulfasalazine; Sulfate radical; UV 254 nm;

    机译:过氧二硫酸盐;光解;柳氮磺胺吡啶;硫酸根;UV 254 nm;

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