An evaluation was made of the feasibility of using reversed-phase liquid chromatography/tandem mass spectrometry with an electrospray interface (LC/ESI-MS/MS) to measure traces of phenoxyacid herbicides and their metabolites in surface and drinking water samples. The procedure involved passing 0.5 L of river and drinking water samples through a 0.5 g graphitized carbon black (GCB) extraction cartridge. Recovery was higher than 85% irrespective of the aqueous matrix in which the analytes were dissolved. A conventional 4.6-mm i.d. reversed-phase LC C-18 column operating with a mobile phase flow rate of 1 mL/min was used to chromatograph the analytes. A flow of 200 microL/min of the column effluent was diverted to the ESI source. The limits of detection (signal-to-noise ratio = 3) of the method for the pesticides considered in drinking and surface water samples are less than 0.1 ng/L for phenoxyacid herbicides, and about 5-10 ng/L for their metabolites (2,4-dichlorophenol and 4-chloro-2-methylphenol). Copyright 2001 John Wiley & Sons, Ltd.

DETERMINATION OF PHENOXYACIDS HERBICIDES AND THEIR PHENOLIC METABOLITES IN SURFACE AND DRINKING WATER / Marchese, Stefano; Perret, Daniela; Gentili, Alessandra; D'Ascenzo, Giuseppe; A., Faberi. - In: RAPID COMMUNICATIONS IN MASS SPECTROMETRY. - ISSN 0951-4198. - STAMPA. - 16:2(2002), pp. 134-141. [10.1002/rcm.557]

DETERMINATION OF PHENOXYACIDS HERBICIDES AND THEIR PHENOLIC METABOLITES IN SURFACE AND DRINKING WATER

MARCHESE, Stefano;PERRET, Daniela;GENTILI, Alessandra;D'ASCENZO, Giuseppe;
2002

Abstract

An evaluation was made of the feasibility of using reversed-phase liquid chromatography/tandem mass spectrometry with an electrospray interface (LC/ESI-MS/MS) to measure traces of phenoxyacid herbicides and their metabolites in surface and drinking water samples. The procedure involved passing 0.5 L of river and drinking water samples through a 0.5 g graphitized carbon black (GCB) extraction cartridge. Recovery was higher than 85% irrespective of the aqueous matrix in which the analytes were dissolved. A conventional 4.6-mm i.d. reversed-phase LC C-18 column operating with a mobile phase flow rate of 1 mL/min was used to chromatograph the analytes. A flow of 200 microL/min of the column effluent was diverted to the ESI source. The limits of detection (signal-to-noise ratio = 3) of the method for the pesticides considered in drinking and surface water samples are less than 0.1 ng/L for phenoxyacid herbicides, and about 5-10 ng/L for their metabolites (2,4-dichlorophenol and 4-chloro-2-methylphenol). Copyright 2001 John Wiley & Sons, Ltd.
2002
Phenoxyacid herbicides; Surface water; Drinking water; SPE; LC-MS/MS
01 Pubblicazione su rivista::01a Articolo in rivista
DETERMINATION OF PHENOXYACIDS HERBICIDES AND THEIR PHENOLIC METABOLITES IN SURFACE AND DRINKING WATER / Marchese, Stefano; Perret, Daniela; Gentili, Alessandra; D'Ascenzo, Giuseppe; A., Faberi. - In: RAPID COMMUNICATIONS IN MASS SPECTROMETRY. - ISSN 0951-4198. - STAMPA. - 16:2(2002), pp. 134-141. [10.1002/rcm.557]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/252403
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