Monitoring of pesticides in agricultural water and soil samples from Andalusia by liquid chromatography coupled to mass spectrometry

被引:166
作者
Vega, AB [1 ]
Frenich, AG [1 ]
Vidal, JLM [1 ]
机构
[1] Univ Almeria, Dept Analyt Chem, Almeria 04071, Spain
关键词
pesticides; liquid chromatography; mass spectrometry; water; soils analysis;
D O I
10.1016/j.aca.2005.02.003
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This work describes the development of an analytical method for determining 32 pesticides, widely used in agricultural areas from the south of Spain, by liquid chromatography-mass spectrometry (LC-MS) with electrospray ionization (ESI) in positive mode. The chromatographic and the MS parameters of the studied compounds were optimized in order to improve selectivity and sensitivity. The separation was carried out in a C, g column using as mobile phase methanol (MeOH) with 0.01 % acetic acid (A) and 0.01 % acetic acid (B) with a flow of 0.2 mL/min in gradient mode. The molecular ion was selected for the quantification in selective ion monitoring (SIM) mode. A solid-phase extraction (SPE) method with HLB Oasis cartridges was applied to allow preconcentration of the target analytes from water samples. However, extraction of the compounds from soil samples was carried out by sonication using liquid-solid extraction with methanol/water. In addition, a clean-up step by SPE using also HLB Oasis cartridges was necessary for soils. The proposed analytical methodology was validated in the target environmental matrices by the analysis of spiked blank matrix samples. Detection limits (LOD) varied between 10 and 50 ng/L for water and 0.5-2.5 mu g/kg for soils, while quantification limits (LOQ) ranged from 25 to 50 ng/L for water and 1.5 to 5.0 mu g/kg for soils. Good recoveries (60-110%) and precision values (< 15%) were obtained for all compounds in the target matrices. This methodology has been successfully applied to the analysis of incurred water and soil samples from agricultural areas of Andalusia (south Spain). The results revealed the presence of some pesticides at several concentration levels both in the soil and water samples. Carbendazim, simazine and diuron were the pesticides most frequently detected in water samples, while only the herbicides simazine, diuron and terbutylazine were found in soil samples. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:117 / 127
页数:11
相关论文
共 25 条
[1]   Monitoring of pesticides in river water based on samples previously stored in polymeric cartridges followed by on-line solid-phase extraction liquid chromatography diode array detection and confirmation by atmospheric pressure chemical ionization mass spectrometry [J].
Aguilar, C ;
Ferrer, I ;
Borrull, F ;
Marcé, RM ;
Barceló, D .
ANALYTICA CHIMICA ACTA, 1999, 386 (03) :237-248
[2]   Determination of pesticides and their degradation products in soil:: critical review and comparison of methods [J].
Andreu, V ;
Picó, Y .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2004, 23 (10-11) :772-789
[3]  
[Anonymous], ENV ANAL CHEM
[4]  
*COUNC EUR COMM, 2001, OFF J EUR COMM L, V331
[5]  
*COUNC EUR COMM, 2000, OFF J EUR COMMUN L, V327
[6]   Hot phosphate-buffered water extraction coupled on line with liquid chromatography/mass spectrometry for analyzing contaminants in soil [J].
Crescenzi, C ;
Di Corcia, A ;
Nazzari, M ;
Samperi, R .
ANALYTICAL CHEMISTRY, 2000, 72 (14) :3050-3055
[7]   Solid-phase extraction followed by high-performance liquid chromatography-ionspray interface-mass spectrometry for monitoring of herbicides in environmental water [J].
Curini, R ;
Gentili, A ;
Marchese, S ;
Marino, A ;
Perret, D .
JOURNAL OF CHROMATOGRAPHY A, 2000, 874 (02) :187-198
[8]   Solid-phase extraction clean-up of soil and sediment extracts for the determination of various types of pollutants in a single run [J].
Dabrowska, H ;
Dabrowski, L ;
Biziuk, M ;
Gaca, J ;
Namiesnik, J .
JOURNAL OF CHROMATOGRAPHY A, 2003, 1003 (1-2) :29-42
[9]  
*EC GUID, 2000, 9188VI97REV8 EC GUID
[10]  
Frenich AG, 2001, J AOAC INT, V84, P1751