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Occurrence and fate of the angiotensin Ⅱ receptor antagonist transformation product valsartan acid in the water cycle - A comparative study with selected β-blockers and the persistent anthropogenic wastewater indicators carbamazepine and acesulfame

机译:血管紧张素Ⅱ受体拮抗剂转化产物缬沙坦酸在水循环中的发生和命运-选定的β受体阻滞剂和持久性人为废水指标卡马西平和乙酰磺胺嘧啶的比较研究

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摘要

The substantial transformation of the angiotensin II receptor antagonist ualsartan to the transformation product 2'-(2H-tetrazol-5-yl)-[l,l'-biphenyl]-4-carboxylic acid (referred to as ualsartan acid) during the activated sludge process was demonstrated in the literature and confirmed in the here presented study. However, there was a severe lack of knowledge regarding the occurrence and fate of this compound in surface water and its behavior during drinking water treatment. In this work a comparative study on the occurrence and persistency of valsartan acid, three frequently used β-blockers (meto-prolol, atenolol, and sotalol), atenolol acid (one significant transformation product of atenolol and metoprolol), and the two widely distributed persistent anthropogenic wastewater indicators carbamazepine and acesulfame in raw sewage, treated waste water, surface water, groundwater, and tap water is presented. Median concentrations of valsartan acid in the analyzed matrices were 101, 1,310, 69, <1.0, and 65 ng L ~1, respectively. Treated effluents from wastewater treatment plants were confirmed as significant source. Regarding concentration levels of pharmaceutical residues in surface waters valsartan acid was found just as relevant as the analyzed (3-blockers and the anticonvulsant carbamazepine. Regarding its persistency in surface waters it was comparable to carbamazepine and acesulfame. Furthermore, removal of valsartan acid during bank filtration was poor, which demonstrated the relevance of this compound for drinking water suppliers. Regarding drinking water treatment {Muelheim Process) the compound was resistant to ozonation but effectively eliminated (>90%) by subsequent activated carbon filtration. However, without applying activated carbon filtration the compound may enter the drinking water distribution system as it was demonstrated for Berlin tap water.
机译:在激活过程中,血管紧张素II受体拮抗剂ualsartan大量转化为2'-(2H-四唑-5-基)-[l,l'-联苯] -4-羧酸(称为ualsartan酸)转化产物污泥过程已在文献中得到证实,并在本文提出的研究中得到证实。但是,对于这种化合物在地表水中的发生和去向及其在饮用水处理过程中的行为,缺乏足够的知识。在这项工作中,比较了缬沙坦酸,三种常用的β受体阻滞剂(美托洛尔,阿替洛尔和索他洛尔),阿替洛尔酸(阿替洛尔和美托洛尔的一种重要转化产物)和缬沙坦酸的发生和持久性的比较研究。给出了持久性人为废水指标,包括原污水,经处理的废水,地表水,地下水和自来水中的卡马西平和乙酰磺胺酸。分析基质中缬沙坦酸的中位数浓度分别为101、1310、69,<1.0和65 ng L〜1。来自废水处理厂的处理后废水被确认为重要来源。关于地表水中药物残留物的浓度水平,发现缬沙坦酸与分析结果同样相关(3-阻滞剂和抗惊厥药卡马西平。就其在地表水中的持久性而言,与卡马西平和乙酰磺胺具有可比性。此外,在储存期间去除了缬沙坦酸过滤效果不佳,证明该化合物对饮用水供应商具有重要意义;就饮用水处理(穆尔海姆工艺)而言,该化合物具有抗臭氧化作用,但可通过随后的活性炭过滤有效去除(> 90%)。但是,如果不应用活性炭过滤,该化合物可能会进入饮用水分配系统,如柏林自来水所证明的那样。

著录项

  • 来源
    《Water Research》 |2013年第17期|6650-6659|共10页
  • 作者单位

    Geoscience Center of the University of Goettingen, Dept. Applied Geology, Goldschmidtstr. 3, 37077 Goettingen,Germany;

    Geoscience Center of the University of Goettingen, Dept. Applied Geology, Goldschmidtstr. 3, 37077 Goettingen,Germany;

    Geoscience Center of the University of Goettingen, Dept. Applied Geology, Goldschmidtstr. 3, 37077 Goettingen,Germany;

    IWW Water Centre, Dept. of Applied Microbiology, Moritzstrasse 26, 45476 Muelheim an der Ruhr, Germany;

    Technische Universitaet Berlin, Dept. of Applied Geosciences, Hydrogeology Research Group, Emst-Reuter-Platz 1,10587 Berlin, Germany;

    Technische Universitaet Berlin, Dept. of Applied Geosciences, Hydrogeology Research Group, Emst-Reuter-Platz 1,10587 Berlin, Germany;

    IWW Water Centre, Dept. of Applied Microbiology, Moritzstrasse 26, 45476 Muelheim an der Ruhr, Germany;

  • 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

    Valsartan acid; Beta-blockers; Acesulfame; Carbamazepine; Water treatment; Surface water;

    机译:缬沙坦酸;Beta阻滞剂;乙磺胺;卡马西平;水处理;地表水;
  • 入库时间 2022-08-17 13:45:41

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