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Fate of pharmaceuticals in drinking water utilities.

机译:饮用水公用事业中药品的命运。

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摘要

Studies suggest that drinking water treatment is effective at decreasing the amount of pharmaceuticals present in source water. Primary treatment processes such as coagulation and sedimentation are not effective on their own, while a combination of filtration and disinfection processes is effective at reducing the concentrations of most pharmaceuticals. The type of oxidant used also determines the degree at which a pharmaceutical is removed from source water. Ozone or the combination of ultraviolet (UV) light with hydrogen peroxide seem to be the most effective oxidation processes. Chlorine oxidation is known to produce chlorinated byproducts when it reacts with organic compounds. In bench-scale studies, the reaction of the pharmaceutical, acetaminophen with free chlorine was studied. Acetaminophen reacts with free chlorine to produce the byproduct 1,4-benzoquinone. Results indicate that acetaminophen is most reactive with free chlorine at pH 9.0 and least reactive at pH 6.0. As pH increased, degradation of acetaminophen also increased. The formation of 1,4-benzoquinone was also affected by pH and reached a maximum of 68.7% of the initial acetaminophen concentration when the pH was at 6.0, the molar ratio at 1,275, and after a contact time of 30 minutes. At all pH values the rate of degradation of acetaminophen was slowest at a molar ratio of about 100, and the highest at a molar ratio of about 10,000.
机译:研究表明,饮用水处理可有效减少源水中存在的药物量。诸如凝结和沉淀之类的初级处理过程本身并不有效,而过滤和消毒过程相结合可有效降低大多数药物的浓度。所用氧化剂的类型还决定了从水源中去除药物的程度。臭氧或紫外线(UV)与过氧化氢的结合似乎是最有效的氧化过程。当氯氧化与有机化合物反应时,它会产生氯代副产物。在实验室规模的研究中,研究了对乙酰氨基酚与游离氯的反应。对乙酰氨基酚与游离氯反应生成副产物1,4-苯醌。结果表明,对乙酰氨基酚在pH 9.0时与游离氯反应最快,在pH 6.0时反应最少。随着pH的增加,对乙酰氨基酚的降解也增加。 1,4-苯醌的形成也受到pH的影响,当pH为6.0时,摩尔比为1,275,且接触时间为30分钟后,最大达到对乙酰氨基酚初始浓度的68.7%。在所有pH值下,对乙酰氨基酚的降解速率在约100的摩尔比下最慢,而在约10,000的摩尔比下最高。

著录项

  • 作者

    Hullman, Rebecca.;

  • 作者单位

    Michigan State University.;

  • 授予单位 Michigan State University.;
  • 学科 Engineering Environmental.
  • 学位 M.S.
  • 年度 2009
  • 页码 90 p.
  • 总页数 90
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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