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Application of excitation-emission matrix fluorescence combined with second-order calibration algorithm for the determination of five polycyclic aromatic hydrocarbons simultaneously in drinking water

机译:激发发射矩阵荧光结合二阶校正算法在同时测定饮用水中五种多环芳烃中的应用

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摘要

Direct determination of five polycyclic aromatic hydrocarbons including fluorene, anthracene, phenanthrene, pyrene and fluoranthene was accomplished by excitation-emission matrix fluorescence coupled with chemometric methods based on an alternating trilinear decomposition (ATLD) algorithm. A uniform design and orthogonal design are proposed for the creation of the calibration set. Results showed that no significant difference in the recoveries for each of the PAHs was observed. Thus, both of the designs can be used for the calibration set. In addition, some statistical parameters and figures of merit, such as average recovery, root-mean-square error of prediction, sensitivity, and selectivity were investigated to evalute the performance of the proposed method. The results showed that fluoranthene was the most selective, whereas fluorene was more sensitive than any other compound. This method was also employed for the determination of samples of drinking water spiked with all these PAHs. It can be observed that the results were not as satisfying as those in synthetic samples due to the negative effects of humic acid or fulvic acid in drinking water.
机译:通过基于交替三线性分解(ATLD)算法的激发发射矩阵荧光与化学计量学方法结合,直接测定了包括芴,蒽,菲,pyr和荧蒽在内的五种多环芳烃。提出了统一的设计和正交设计以创建校准集。结果表明,每种多环芳烃的回收率均无显着差异。因此,这两种设计都可以用于校准集。此外,还研究了一些统计参数和优值,例如平均回收率,预测的均方根误差,灵敏度和选择性,以评估该方法的性能。结果表明,荧蒽的选择性最高,而芴比其他任何化合物都要敏感。该方法还用于测定所有这些多环芳烃加标的饮用水样品。可以看出,由于饮用水中腐殖酸或黄腐酸的负面影响,结果不如合成样品令人满意。

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