A Comparison of the Performance of Two Chromatographic and Three Extraction Techniques for the Analysis of PAHs in Sources of Drinking Water

The aim of this work is to establish a sensitive and reliable method for the analysis of the 16 priority Environmental Protection Agency-defined polycyclic aromatic hydrocarbons (PAHs) found in water samples. Gas chromatography (GC)-mass spectrometry (MS) and high-performance liquid chromatography (...

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Published inJournal of chromatographic science Vol. 45; no. 2; pp. 57 - 62
Main Authors Díaz-Moroles, Nora E., Garza-Ulloa, Humberto J., Castro-Ríos, Rocío, Ramírez-Villarreal, Elsa G., Barbarín-Castillo, Juan M., dela Luz Salazar-Cavazos, María, Waksman-de Torres, Noemí
Format Journal Article
LanguageEnglish
Published Niles, IL Oxford University Press 01.02.2007
Preston Publications
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Summary:The aim of this work is to establish a sensitive and reliable method for the analysis of the 16 priority Environmental Protection Agency-defined polycyclic aromatic hydrocarbons (PAHs) found in water samples. Gas chromatography (GC)-mass spectrometry (MS) and high-performance liquid chromatography (HPLC)-fluorescence detection (FLD)-UV techniques are optimized to obtain an adequate resolution of all compounds. Validation of the methods is carried out, and a good performance is observed for both techniques. The HPLC-FLD-UV technique is somewhat more sensitive than the GC-MS technique for the determination of PAHs; thus, the HPLC-FLD-UV method is used to follow up both the solid-phase extraction (SPE) analysis using cartridges and discs and the liquid-liquid extraction (LLE), which are also evaluated for the extraction of the PAHs. Low recoveries between 43% and 79% are obtained using SPE cartridges, and higher values are obtained using SPE discs (56-96%) and LLE (60-105%). Better results are obtained using the LLE technique, and, thus, analysis of real water samples is carried out using this technique. LODs between 0.6 and 21 ng/L and relative standard deviations less than 15% are obtained using a spiked water sample analyzed using the full LLE HPLC-FLD-UV method.
Bibliography:ark:/67375/HXZ-9CL91TTM-9
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ISSN:0021-9665
1945-239X
DOI:10.1093/chromsci/45.2.57