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Photochemical Fate and Advanced Oxidation Treatment of Pharmaceuticals in Water.

机译:水中药物的光化学命运和高级氧化处理。

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摘要

This work focuses on two broad areas: the photochemical fate of pharmaceutical compounds in the environment and advanced oxidation technologies designed to remove them from the water supply.;Advanced oxidation processes have been shown to hold potential for the removal of emerging contaminants of concern from water samples in an efficient and economical manner. These processes are based on the production of a reactive species, such as the hydroxyl radical or hydrated electron, which then reacts with, and breaks down, the pharmaceutical molecule. Using fluoroquinolones and antidepressants as representative sets of pharmaceuticals, the hydroxyl radical and hydrated electron were both found to rapidly react with these compounds (∼109-1010 M-1 s-1). Several byproducts and degradation pathways were identified.;While the hydroxyl radical and hydrated electron both react rapidly with organic compounds, the hydroxyl radical plays a larger role in the degradation of pharmaceuticals in surface waters, due to its higher steady state concentration in the natural environment. This was demonstrated for three antidepressant compounds. Experiments were also performed to analyze the role of singlet oxygen, whose contribution to the degradation is approximately an order of magnitude lower than that of the hydroxyl radical.;In addition to reactive oxygen species, excited state natural organic matter may also contribute to the photochemical degradation of pharmaceutical compounds. To measure the rate constants between excited triplet state natural organic matter and pharmaceutical compounds, the excited state was generated by laser flash photolysis at 355 nm and the decay of the transient excited state species absorption was monitored at 525 nm. Rate constants were found to be on the order of 108-109 M-1 s-1, indicating that excited triplet state natural organic matter reacts rapidly with these pharmaceuticals and, if present in the environment, may contribute substantially to their photochemical degradation.;This work represents a small step in the quest to describe and understand the behavior of pharmaceutical compounds in the natural environment and in engineered treatment systems. It is hoped that this knowledge will contribute to the eventual ability to ensure that these compounds are removed from our water supply.
机译:这项工作着眼于两个广泛的领域:环境中药物化合物的光化学命运以及旨在将其从供水系统中去除的先进氧化技术。业已表明,先进的氧化工艺具有从水中去除新出现的污染物的潜力以有效且经济的方式进行采样。这些过程基于反应性物质(例如羟基自由基或水合电子)的产生,然后与药物分子发生反应并分解。使用氟喹诺酮类和抗抑郁药作为代表性药物,发现羟基自由基和水合电子均会与这些化合物快速反应(〜109-1010 M-1 s-1)。鉴定了几种副产物和降解途径。羟自由基和水合电子均与有机化合物快速反应,但羟自由基在地表水中的药物降解由于其在自然环境中的较高稳态浓度而起较大作用。 。对于三种抗抑郁化合物已证明了这一点。还进行了实验以分析单线态氧的作用,其对降解的贡献比羟基自由基的贡献低约一个数量级。除了活性氧以外,激发态天然有机物也可能对光化学有贡献。药物化合物的降解。为了测量激发的三重态天然有机物与药物化合物之间的速率常数,通过在355 nm处进行激光闪光光解产生激发态,并在525 nm处监测瞬态激发态物质吸收的衰减。发现速率常数约为108-109 M-1 s-1,表明激发的三重态天然有机物与这些药物迅速反应,如果存在于环境中,则可能对其光化学降解有很大贡献。这项工作代表了描述和理解药物化合物在自然环境和工程处理系统中的行为的一小步。希望这些知识将有助于确保从我们的供水中清除这些化合物的最终能力。

著录项

  • 作者

    Santoke, Hanoz.;

  • 作者单位

    University of California, Irvine.;

  • 授予单位 University of California, Irvine.;
  • 学科 Engineering Environmental.;Chemistry Physical.;Environmental Health.;Water Resource Management.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 99 p.
  • 总页数 99
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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