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Evaluation of ozone-based treatment processes for wastewater containing microcontaminants using LC-QTRAP-MS and LC-TOF/MS

机译:使用LC-QTRAP-MS和LC-TOF / MS评估含微污染物废水的臭氧处理工艺

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This article describes the development of an enhanced liquid chromatography-mass spectrometry (LC-MS) method for the analysis of a selected group of 57 organic contaminants in wastewater This. group comprises 39 pharmaceuticals belonging to different therapeutical classes and 10 of their most frequent metabolites. Six pesticides and two disinfectants were also included. The LC-MS method was developed using a hybrid quad rupole/linearion trap (Q TRAP) analyzer operating in selected reaction monitoring (SRM) mode (in both positive and negative electrospray ionization) in combination with a time-of flight (TOF) mass analyser. The application of both techniques provided very good results in terms of accurate quantification and unequivocal identification. Quantification was based on the use of a linearly accelerating (LINAC) high-pressure collision cell, which enable the analysis of a high number of compounds with enough acquisition data points for an optimal peak definition in SRM. Unequivocal identification was provided by the acquisition of at least two SRM transitions and by obtaining accurate mass measurements of the identified compounds with errors lower than 2 ppm. As an alternative for compounds where a second transition cannot be detected by Q-Trap-MS, the application of survey scans in enhanced product ion (EPI) was evaluated. The analytical performance of the method was evaluated in effluent wastewater samples. Linearity of response over three orders of magnitude was demonstrated (R-2 > 0.99 for most compounds). matrix effects resulting in suppression of the response were frequently observed, between 2-50% for most of compounds, except 4-DAA and 4-AA, which exhibit higher values (68%). Signal enhancement was also detected in 16 compounds. Method limits of detection (LOD) were between 0.1-50 ng L-1. Finally, the methodology was successfully applied to the evaluation of the efficiency of two ozone-based treatments applied to the effluent from the secondary clarifier of a municipal wastewater treatment facility. Preliminary results are presented demonstrating that ozonation of wastewaters degrade pharmaceuticals with a high efficiency. Removals higher than 90% were reached for most of target analytes.
机译:本文介绍了一种增强型液相色谱-质谱(LC-MS)方法的开发方法,该方法用于分析废水中选定的57种有机污染物。该组包括39种属于不同治疗类别的药物和10种最常见的代谢物。还包括六种农药和两种消毒剂。 LC-MS方法是使用混合四极杆/线性离子阱(Q TRAP)分析仪开发的,该分析仪以选定的反应监测(SRM)模式(正电喷雾和负电喷雾电离)结合飞行时间(TOF)质量运行分析器。两种技术的应用在准确定量和明确鉴定方面都提供了很好的结果。定量基于线性加速(LINAC)高压碰撞池的使用,该池可分析大量化合物,并具有足够的采集数据点,以实现SRM中的最佳峰定义。通过采集至少两个SRM跃迁以及通过获得误差小于2 ppm的已鉴定化合物的准确质量测量值,可以进行明确鉴定。作为无法通过Q-Trap-MS检测到第二次跃迁的化合物的替代方法,评估了扫描扫描在增强产物离子(EPI)中的应用。在废水样品中评估了该方法的分析性能。证实了三个数量级以上的响应线性(大多数化合物的R-2> 0.99)。经常观察到导致抑制响应的基质效应,大多数化合物的2-50%除外,除了4-DAA和4-AA表现出更高的值(68%)。在16种化合物中也检测到信号增强。方法的检出限(LOD)在0.1-50 ng L-1之间。最后,该方法成功地应用于评估两种臭氧处理方法的效率,该方法适用于市政废水处理设施二级澄清池的废水。初步结果表明,废水的臭氧化可高效降解药物。大多数目标分析物的去除率均高于90%。

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