On-line solid phase extraction-liquid chromatography-mass spectrometry for trace determination of nerve agent degradation products in water samples

Forfatter
Røen, Bent Tore
Sellevåg, Stig Rune
Lundanes, Elsa
Publisert
2013
Emneord
Nervemidler
Permalenke
https://ffi-publikasjoner.archive.knowledgearc.net/handle/20.500.12242/467
DOI
10.1016/j.aca.2012.11.053
Samling
Articles
Description
Røen, Bent Tore; Sellevåg, Stig Rune; Lundanes, Elsa. On-line solid phase extraction-liquid chromatography-mass spectrometry for trace determination of nerve agent degradation products in water samples. Analytica Chimica Acta 2013 ;Volum 761. s. 109-116
1024568.pdf
Size: 743k
Sammendrag
Three primary nerve agent degradation products (ethyl-, isopropyl- and pinacolyl methylphosphonic acid) have been determined in water samples using on-line solid phase extraction-liquid chromatography and mass spectrometry (SPE-LC–MS) with electrospray ionisation. Porous graphitic carbon was employed for analyte enrichment followed by hydrophilic interaction chromatography. Diethylphosphate was applied as internal standard for quantitative determination of the alkyl methylphosphonic acids (AMPAs). By treating the samples with strong cation-exhange columns on Ba, Ag and H form, the major inorganic anions in water were removed by precipitation prior to the SPE-LC–MS determination. The AMPAs could be determined in tap water with limits of detection of 0.01–0.07 μg L−1 with the [M−H]− ions extracted at an accuracy of ±5 mDa. The within and between assay precisions at analyte concentrations of 5 μg L−1 were 2–3%, and 5–9% relative standard deviation, respectively. The developed method was employed for determination of the AMPAs in three natural waters and a simulated waste water sample, spiked at 5 μg L−1. Recoveries of ethyl-, isopropyl- and pinacolyl methylphosphonic acid were 80–91%, 92–103% and 99–106%, respectively, proving the applicability of the technique for natural waters of various origins.
View Meta Data