Determination of phenoxyacid herbicides and their phenolic metabolites in surface and drinking water
Stefano Marchese1, Daniela Perret, Alessandra Gentili
1Laboratorio Chimico per la Sicurezza, Dipartimento di Chimica, Università La Sapienza di Roma, Piazzale Aldo Moro n degrees 5, P.O. Box 34, Posta 62, 00185 Roma, Italy. stefano.marchese@uniroma.1.it
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).

