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Fluorescence excitation emission matrices for rapid detection of polycyclic aromatic hydrocarbons and pesticides in surface waters

机译:荧光激发发射矩阵可快速检测地表水中的多环芳烃和农药

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摘要

Application of real-time fluorescence excitation emission matrices (EEM) as a tool for water quality assessment was investigated. A bench-scale fluorescence system with on-line monitoring capabilities was used to quantify several polycyclic aromatic hydrocarbons (PAHs) and pesticides in surface waters of Ontario, Canada. Parallel factors analysis (PARAFAC), an unsupervised multi-way analysis approach, was compared to a supervised peak-picking approach. Both approaches produced sensitive regression models capable of predicting contaminant concentration with mean absolute errors (MAE) that ranged from 0.032 to 0.293 mu g L-1 for lake water, and 0.052 to 0.921 mu g L-1 for river water. In addition, results showed accurate detection of contaminant concentrations exceeding 0.25 mu g L-1. However, concentration and variability of natural organic matter (NOM) in natural waters presented unique challenges to peak-picking, PARAFAC, and regression analysis, which were mitigated by expert supervision as well as site-specific and timely calibration.
机译:研究了实时荧光激发发射矩阵(EEM)作为水质评估工具的应用。具有在线监测功能的台式荧光系统用于定量加拿大安大略省地表水中的几种多环芳烃(PAH)和农药。并行因素分析(PARAFAC)是一种无监督的多向分析方法,与一种有监督的峰提取方法进行了比较。两种方法均产生了灵敏的回归模型,能够预测污染物浓度,其中湖水的平均绝对误差(MAE)在0.032至0.293μg L-1之间,河水在0.052至0.921μgL-1之间。此外,结果表明可以准确检测出超过0.25μg L-1的污染物浓度。但是,天然水中天然有机物(NOM)的浓度和变异性对采摘峰,PARAFAC和回归分析提出了独特的挑战,这些挑战可以通过专家监督以及针对具体地点的及时校准得到缓解。

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    Univ Toronto, Dept Civil & Mineral Engn, 35 St George St, Toronto, ON M5S 1A4, Canada;

    Univ British Columbia Okanagan, Sch Engn, 1137 Alumni Ave, Kelowna, BC V1V 1V7, Canada;

    Univ Waterloo, Dept Chem Engn, 200 Univ Ave W, Waterloo, ON N2L 3G1, Canada;

    Univ Toronto, Dept Civil & Mineral Engn, 35 St George St, Toronto, ON M5S 1A4, Canada;

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