2012
DOI: 10.1016/j.talanta.2012.05.032
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Analysis of N-nitrosamines in water by isotope dilution gas chromatography–electron ionisation tandem mass spectrometry

Abstract: , S. J. (2012). Analysis of N-nitrosamines in water by isotope dilution gas chromatography-electron ionisation tandem mass spectrometry. Talanta, Analysis of N-nitrosamines in water by isotope dilution gas chromatography-electron ionisation tandem mass spectrometry a b s t r a c t A method has been developed for the determination of eight N-nitrosamines in drinking water and treated municipal effluent. The method uses solid phase extraction (SPE), gas chromatography (GC) and analysis by tandem mass spectrometr… Show more

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Cited by 74 publications
(42 citation statements)
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References 22 publications
(27 reference statements)
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“…N-nitrosamine concentrations were determined based on the analytical method previously developed by McDonald et al [24]. The analytical method includes solid phase extraction (SPE) followed by gas chromatography and quantification using tandem mass spectrometry and isotope dilution.…”
Section: Methodsmentioning
confidence: 99%
“…N-nitrosamine concentrations were determined based on the analytical method previously developed by McDonald et al [24]. The analytical method includes solid phase extraction (SPE) followed by gas chromatography and quantification using tandem mass spectrometry and isotope dilution.…”
Section: Methodsmentioning
confidence: 99%
“…McDonald et al [28], which involves solid phase extraction (SPE) and subsequent quantification by gas chromatography -tandem mass spectrometry (GC-MS/MS) with electron ionisation. Prior to GC-MS/MS analysis, 200 mL of sample was extracted to a Supelclean TM Coconut Charcoal (2 g) SPE cartridge (Supelco, St Louis, MO, USA).…”
Section: N-nitrosamine Analysismentioning
confidence: 99%
“…McDonald et al [13] dried sorbent cartridges using a gentle stream of nitrogen rather than a vacuum, but they did not mention the flow rate or pressure used, nor whether the sorbent became completely dry. It appears that the sorbent may not have become completely dry, because their recovery rates were lower than the recovery rates achieved using our method and because the recovery rates ranged widely, from 68% at 10 ng/L to 102% at 100 ng/L.…”
Section: Methods Validationmentioning
confidence: 99%