Multiresidue determination of pesticides in drinking and related waters by gas chromatography/mass spectrometry after solid-phase extraction: Interlaboratory study (original) (raw)
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Analytical and Bioanalytical Chemistry, 2008
European Council Directive 98/83/EC on the quality of water intended for human consumption brought a new challenge for water-quality control routine laboratories, mainly on pesticides analysis. Under the guidelines of ISO/ IEC 17025:2005, a multiresidue method was developed, validated, implemented in routine, and studied with real samples during a one-year period. The proposed method enables routine laboratories to handle a large number of samples, since 28 pesticides of 14 different chemical groups can be quantitated in a single procedure. The method comprises a solid-phase extraction step and subsequent analysis by liquid chromatography-mass spectrometry (LC-MS-MS). The accuracy was established on the basis of participation in interlaboratory proficiency tests, with encouraging results (majority |z-score| <2), and the precision was consistently analysed over one year. The limits of quantitation (below 0.050 μg L −1) are in agreement with the enforced threshold value for pesticides of 0.10 μg L −1. Overall method performance is suitable for routine use according to accreditation rules, taking into account the data collected over one year.
Journal of Liquid Chromatography & Related Technologies, 2005
Os pesticidas organofosforados são freqüentemente aplicados no cultivo de tomate no Brasil. No presente trabalho uma metodologia analítica foi desenvolvida e validada para a quantificação de resíduos dos pesticidas organofosforados acefato, chlorpyrifós, malation, metamidofós and paration metílico em tomate, empregando Cromatografia Gasosa com Detector de Nitrogênio e Fósforo (GC-NPD). A possibilidade de ocorrência de efeito matriz foi estudada. As curvas analíticas, preparadas nos extratos da matriz, foram lineares de 0,006 até 0,80 mg L -1 . Os estudos de precisão forneceram resultados com RSD <15%. As recuperações dos pesticidas, obtidas com as curvas preparadas no extrato da matriz, foram entre 88 e 118%. Com o procedimento proposto foram obtidos limites de quantificação entre 0,0132 e 0,135 mg kg -1 .
Journal of Chromatography A, 1990
An automated reversed-phase high-performance liquid chromatographic (HPLC) method has been developed for the determination of trace concentrations of propoxur, carbofuran, carbaryl, propham, captan, chloropropham, barban and butylate in drinking water. A lOO-ml of sample water is passed through a 3-cm precolumn, packed with 5-pm ODS sorbent, at a flow-rate of 5 ml/min. The HPLC system is then switched to an acetonitrile-water gradient elution program. The analytes, which are concentrated on the precolumn, are eluted and separated on a 25-cm C8 analytical column and determined by measuring the UV absorption at 220 nm. The resolution of analytes is excellent regardless of whether the elution from the precolumn is done unidirectionally or with backflushing. The precolumn can be used repeatedly for at least 30 samples without a significant decrease in efficiency. The total analytical time is 60 min. Tap, distilled, deionized, commercial spring and HPLC-grade waters were analyzed. The lowest detectable concentrations are in the range of 10. 10-'2-460 lo-r2 g/ml for the eight pesticides with 100 ml of sample.
Journal of the Brazilian Chemical Society, 2015
In this work, a method for multiclass determination of 70 pesticides residues with different properties in drinking water using solid phase extraction (SPE) with polymeric sorbent and determination by gas and liquid chromatography coupled to tandem mass spectrometry (GC-MS/MS and LC-MS/MS) was developed and validated. Different sample volumes, sorbents and elution solvents were evaluated. The best results were obtained using the sorbent Oasis ® HLB, sample acidified at pH 2.5 and a mixture of dichloromethane/methanol as eluent. The limit of quantification (LOD) of the method was 0.02 µg L-1 for aldrin, dieldrin and chlordane and 0.5 µg L-1 for the other compounds. Satisfactory accuracy, with recoveries between 70 and 117.3%, and good precision, with relative standard deviation (RSD) values below 19.7% for most of the compounds, were achieved. The validated method was applied to real water samples and results indicated that the proposed method is suitable for the determination of pesticide residues in water samples.
Journal of the Brazilian Chemical Society, 2010
Um método analítico baseado na extração em fase sólida e cromatografia líquida acoplada à espectrometria de massas tandem (LC-ESI-MS-MS) foi desenvolvido e validado para a determinação e confirmação de dezoito agrotóxicos (herbicidas, inseticidas e fungicidas) e dois metabólitos em amostras de água. Os limites de detecção variaram de 0,4 a 40,0 ng L -1 e os limites de quantificação de 4,0 a 100,0 ng L -1 . Foi obtida boa linearidade, com r 2 > 0,99 para todos os compostos. As recuperações, para 95% dos compostos, variaram de 70 a 120%, com RSDs menores que 21% para todos. Através do monitoramento de reações múltiplas (MRM), foram selecionadas duas diferentes transições íon precursor-íon produto para cada agrotóxico. A metodologia proposta pode ser usada para a determinação de resíduos de agrotóxicos em águas de superfície e potável, em concordância com a Lei n° 518 do Ministério da Saúde, Brasil, e com os parâmetros da União Européia para água potável (Directive 98/83/EC).
A multiresidue method for determination of trace levels of pesticides in air and water
Archives of Environmental Contamination and Toxicology, 1996
A multiresidue analytical method is described for the analysis of 13 pesticides in fogwater, rainwater, gas, and particles. This method is based upon solid-liquid extraction using Sep-Pak TM tC~8 light cartridges for aqueous samples, soxhlet for gas (adsorbed on XAD-2 ®) and particles (on glass fiber filters), HPLC-based fractionation of the extracted residues using a silica column, and a linear gradient of n-hexane/tert butyl methyl ether followed by GC-ECD and HPLC-UV analyses of each fraction. Prior to analysis with GC-ECD, a methylation procedure using BFJmethanol was developed for the analysis of the fraction which contains chlorophenoxy acid herbicides. The recoveries of the extraction procedure of liquid samples and of the methylation were greater than 92 and 97% with a standard deviation lower than 8 and 5%, respectively. The detection limits varied between 0.1 and 0.01 I~g • ml t for the 13 pesticides studied with a standard deviation less than 9%. This method was used for the determination of pesticides in 18 fogwater samples (soluble + insoluble), 31 rainwater samples, and 17 air (gas + particles) samples collected between 1991 and 1993 in Colmar (east of France).
Analytical and Bioanalytical Chemistry, 2011
Effluent from wastewater treatment plants have been identified as an important source of micro-organic contaminants in the environment. An online highperformance liquid chromatography-heated electrospray ionization tandem mass spectrometric method was developed and validated for the determination of basic pesticides in effluent wastewaters. Most available methods for pesticide analysis of wastewater samples are time-consuming, require complex clean-up steps and are difficult to automate. The method developed used a simple solid-phase extraction clean-up for salt and lipid reduction. On-line sample pre-concentration was performed using a reversed phase (C 18 ) column, and analytes were separated by back-flushing onto an analytical column (C 8 ) with detection using QqQ MS. An option to increase MS resolution was exploited to minimize interference from endogenous compounds in the matrix. A better than unit mass resolution was used (Q1 full width half maximum (FWHM)=0.2 Da and Q3 FWHM=0.7 Da), which was as rugged as a unit resolution method, and improved signal/noise and better detection limits were achieved for the targeted basic pesticides. This method was applied to the determination of 11 pesticides, including methoxytriazine, chlorotriazines, chloroacetanilides, phenylurea and carbamate pesticides. The percentage recovery values for these pesticides using the online trapping column were within the range, 73-95%, with relative standard deviation (RSD) values <8.9%. The highest concentrations of these pesticides in wastewater effluents in County Cork, Ireland, were simazine (0.51 μg/L), prometon (0.14 μg/L), diuron (0.21 μg/L) and atrazine (0.19 μg/L).
Analytical and Bioanalytical Chemistry, 2010
An optimised extraction and cleanup method for the analysis of pesticide in natural water samples is presented. Sixteen pesticides of different polarity and from the different chemical classes (organophosphates, triazines, benzimidazoles, carbamates, carbamides, neonicotinoides, methylureas, phenylureas and benzohydrazides), most frequently used in Serbia, were selected for the analysis. Liquid-phase microextraction in a single hollow fibre (HF-LPME) has been applied for sample preparation. The concentrations of pesticides were determined using HPLC-MS/MS method with electrospray ionisation. The extraction behaviour and selection of the experimental conditions was predicted based on log D and pK a values of targeted pesticides, which were calculated applying the computer software ACD/Labs PhysChem Suite v12. The influence of the donor pH and concentration of pesticides, organic phase composition as well as the extraction time on the extraction efficiency was investigated. Optimum extraction conditions were evaluated with respect to the investigated parameters of the extraction. The extraction method was validated for 10 out of 16 studied pesticides. Linear range of the pesticides was 0.1-5 µg L −1 with the correlation coefficient from 0.991 to 0.9998, and the relative standard deviation for three standard measurements was between 0.2 and 11.8%. The limits of detections ranged from 0.026 to 0.237 µg L −1 and the limits of quantifications from 0.094 to 0.793 µg L −1 . The optimised two-phase HF-LPME method was successfully applied for determination of moderately polar as well low-polar pesticides in the environmental water samples.