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

被引:0
作者
Yang, Ye Z. [1 ]
Peleato, Nicolas M. [2 ]
Legge, Raymond L. [3 ]
Andrews, Robert C. [1 ]
机构
[1] Univ Toronto, Dept Civil & Mineral Engn, 35 St George St, Toronto, ON M5S 1A4, Canada
[2] Univ British Columbia Okanagan, Sch Engn, 1137 Alumni Ave, Kelowna, BC V1V 1V7, Canada
[3] Univ Waterloo, Dept Chem Engn, 200 Univ Ave W, Waterloo, ON N2L 3G1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
DISSOLVED ORGANIC-MATTER; PARALLEL FACTOR; NEURAL-NETWORKS; CALIBRATION; SPECTRA; SPECTROSCOPY; WASTE; RIVER; QUANTIFICATION; PARAFAC;
D O I
10.1039/c8ew00821c
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
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.
引用
收藏
页码:315 / 324
页数:10
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