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Chromatographic determination and toxicological potential evaluation of selected micropollutants in aquatic environment-analytical problems

机译:水环境分析问题中某些微量污染物的色谱测定和毒理学潜力评估

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In this study, the analytical procedures for the improved extraction and determination of the selected micropollutants (anthracene, pentachlorophenol, octylphenol, benzo(a)pyrene, and diclofenac) in aqueous environment are proposed. These methods were based on application of gas chromatography coupled with mass spectrometry and solid phase extraction for isolation of tested analytes from water samples. Compared to standard procedures currently used in the range presented in this paper, the authors' modifications of analytical procedures allowed increasing the recovery rate of analytes. Within modification of procedures, hyamine, methanol were used. The substances increase solubility of analytes in water, for instance. Toxicological potential of samples containing tested micropollutants in different environmental matrix was evaluated. Proposed analytical procedures allow the quantitative determination of five different compounds in aquatic environment with satisfactory repeatability and precision of measurements. Applied modifications of analytical procedures had an influence on the increase of recovery degree of compounds. Extraction of micropollutants from effluent exceeded 60% and depended on compounds concentration in the samples, excluding the determination for lower concentration of anthracene. The limits of quantitation LOQ (in ng/L) were as follows: 6.5 for anthracene and octylphenol, 8.5 for diclofenac, and 10 for pentachlorophenol and benzo(a)pyrene. It was found that Microtox((R)) assay allows the quick evaluation of toxicological potential of selected micropollutants. The toxicological potential (expressed as EC50, in mg/L) of deionized water samples containing micropollutants was equal to: 12.8; 2.2; 1.4; 6.6; 23.1 for anthracene, pentachlorophenol, octylphenol, benzo(a)pyrene, and diclofenac, respectively. However, the toxicity was also dependent on environmental matrix. The explanation of this phenomenon requires further research.
机译:在这项研究中,提出了在水性环境中改进萃取和测定所选微量污染物(蒽,五氯苯酚,辛基苯酚,苯并(a)py和双氯芬酸)的分析程序。这些方法基于气相色谱结合质谱和固相萃取的应用,用于从水样中分离出被测分析物。与本文中介绍的当前标准程序相比,作者对分析程序的修改允许提高分析物的回收率。在修改程序的范围内,使用了氨基,甲醇。例如,这些物质会增加分析物在水中的溶解度。评估了在不同环境基质中含有测试的微污染物的样品的毒理学潜力。拟议的分析程序可以定量测定水生环境中的五种不同化合物,并具有令人满意的重复性和测量精度。分析方法的应用修改对化合物回收率的提高有影响。从废水中提取微污染物的比例超过60%,并取决于样品中化合物的浓度,其中不包括较低浓度蒽的测定。 LOQ的定量限(以ng / L为单位):蒽和辛基苯酚为6.5,双氯芬酸为8.5,五氯苯酚和苯并(a)re为10。发现Microtox(R)测定法可以快速评估所选微污染物的毒理学潜力。含有微量污染物的去离子水样品的毒理学潜力(以mg / L表示为EC50)等于:12.8; 2.2; 1.4; 6.6;蒽,五氯苯酚,辛基苯酚,苯并(a)py和双氯芬酸分别为23.1。但是,毒性也取决于环境基质。对这种现象的解释需要进一步研究。

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