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The Transformation of Microcystin-LR during Tap Water Treatment Process

机译:自来水处理过程中微囊藻毒素-LR的转化

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Objective To establish a liquid chromatography-tandem mass spectrometry (LC/MS/MS) method for the determination of microcystin-LR (MC-LR) in drinking water, investigate its removal efficiency during tap water advanced treatment process and analyze its degradation products in the tap water. Methods Water samples were collected from each point of tap water advanced treatment process and treated by mixing, filtration, concentration, elution, nitrogen blow and re-dissolvement. The samples were analyzed by LC/MS/MS to determine the MC-LR concentration and its removal efficiency during treatment process. The combination of actual water enrichment and laboratory simulated water were used to qualitative analyze the MC-LR degradation products by Orbitrap mass spectrometry. Results The linearity of MC-LR ranged from 2 pg/L to 200 pg/L with the detection limit of 0.0079 pg/L and the limit of quantification of 0.0263 pg/L. The recovery rate of MC-LR from different contration in drinking water were from 94.88% to 101.47%. The intra-day precision was 2.51%-7.93% and the intra-day precision was 3.24%-8.41%. The average concentration of MC-LR in source water was 0.631 pg/L, 94.0% of which can be removed by ozone exposure, biological pre-treatment and chlorination. The remaining can hardly be removed by sand filtration, ozone exposure, activated carbon, ultrafiltration and other processes. The MC-LR average concentration in the finished water maintained at about 0.036 pg/L. Four degradation products were identified in the laboratory simulated water of the mixture of MC-LR and liquid chlorine in the mass ratio of 1:10. Conclusion the established MC-LR detection method can be well applied to the monitoring of MC-LR in drinking water due to its simple pre-treatment process and good methodological validation parameters. The removal efficiency of treatment processes was different.
机译:目的建立液相色谱-串联质谱(LC / MS / MS)测定饮用水中微囊藻毒素(MC-LR)的方法,研究其在自来水深度处理过程中的去除率,并分析其降解产物。自来水。方法从自来水深度处理过程的每个点收集水样,并通过混合,过滤,浓缩,洗脱,吹氮和再溶解进行处理。通过LC / MS / MS分析样品,以确定在处理过程中MC-LR浓度及其去除效率。结合实际水富集和实验室模拟水,通过Orbitrap质谱法对MC-LR降解产物进行定性分析。结果MC-LR的线性范围为2 pg / L至200 pg / L,检出限为0.0079 pg / L,定量限为0.0263 pg / L。不同饮用水中MC-LR的回收率从94.88%到101.47%。日内精确度为2.51%-7.93%,日内精确度为3.24%-8.41%。原水中MC-LR的平均浓度为0.631 pg / L,其中94.0%可通过暴露于臭氧,生物预处理和氯化来去除。残留物很难通过沙滤,暴露于臭氧,活性炭,超滤和其他工艺除去。最终水中的MC-LR平均浓度保持在约0.036 pg / L。在实验室模拟水中,质量比为1:10的MC-LR和液氯的混合物中鉴定出四种降解产物。结论所建立的MC-LR检测方法预处理过程简单,方法学验证参数良好,可以很好地应用于饮用水中MC-LR的监测。处理过程的去除效率不同。

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