Determination of Selected Pesticide Residues in River Water Using SBSE Technique
The analytical procedure based on stir‑bar sorptive extraction technique, for the determination of selected pesticide residues (diazinon, malathion, cyprodinyl, penconazole, fludioxonyl, pyriproxyfen, boscalid, pyraclostrobin) is described. Analysis was performed using the commercial TwisterTM stir...
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Online Access: | https://acta.mendelu.cz/65/5/1595/ |
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doaj-2d983f3df104493ebf945bc5d63d9b872020-11-24T22:31:23ZengMendel University PressActa Universitatis Agriculturae et Silviculturae Mendelianae Brunensis1211-85162464-83102017-01-016551595159910.11118/actaun201765051595Determination of Selected Pesticide Residues in River Water Using SBSE TechniqueAndrea Purdešová0Slovak University of Technology, Faculty of Chemical and Food Technology, Institute of Analytical Chemistry, Radlinského 9, 812 37 Bratislava, Slovak RepublicThe analytical procedure based on stir‑bar sorptive extraction technique, for the determination of selected pesticide residues (diazinon, malathion, cyprodinyl, penconazole, fludioxonyl, pyriproxyfen, boscalid, pyraclostrobin) is described. Analysis was performed using the commercial TwisterTM stir bar for sorptive extraction. It consists of a 2.0‑cm‑long glass‑encapsulated magnetic stir bar externally coated with PDMS. The extracts were off‑line analyzed using fast GC‑MS in SIM mode. Optimized conditions were established as follows concerning extraction time, stirring speed, aqueous medium characteristics (ionic strength and polarity) respectively: 120 min (700 rpm), addition of 4 g of sodium chloride, no addition of methanol as organic modifier, and 30 min ultrasonic desorption in acetonitrile. Recoveries ranged from 38 % to 58 % (RSD < 15 %, n = 6). Validated limits of quantification in matrix were between 1.6 ngL−1 and 548.8 ngL−1, depending on the compound.https://acta.mendelu.cz/65/5/1595/Fast gas chromatography‑mass spectrometrywaterpesticideselectron ionizationSBSE |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Andrea Purdešová |
spellingShingle |
Andrea Purdešová Determination of Selected Pesticide Residues in River Water Using SBSE Technique Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis Fast gas chromatography‑mass spectrometry water pesticides electron ionization SBSE |
author_facet |
Andrea Purdešová |
author_sort |
Andrea Purdešová |
title |
Determination of Selected Pesticide Residues in River Water Using SBSE Technique |
title_short |
Determination of Selected Pesticide Residues in River Water Using SBSE Technique |
title_full |
Determination of Selected Pesticide Residues in River Water Using SBSE Technique |
title_fullStr |
Determination of Selected Pesticide Residues in River Water Using SBSE Technique |
title_full_unstemmed |
Determination of Selected Pesticide Residues in River Water Using SBSE Technique |
title_sort |
determination of selected pesticide residues in river water using sbse technique |
publisher |
Mendel University Press |
series |
Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis |
issn |
1211-8516 2464-8310 |
publishDate |
2017-01-01 |
description |
The analytical procedure based on stir‑bar sorptive extraction technique, for the determination of selected pesticide residues (diazinon, malathion, cyprodinyl, penconazole, fludioxonyl, pyriproxyfen, boscalid, pyraclostrobin) is described. Analysis was performed using the commercial TwisterTM stir bar for sorptive extraction. It consists of a 2.0‑cm‑long glass‑encapsulated magnetic stir bar externally coated with PDMS. The extracts were off‑line analyzed using fast GC‑MS in SIM mode. Optimized conditions were established as follows concerning extraction time, stirring speed, aqueous medium characteristics (ionic strength and polarity) respectively: 120 min (700 rpm), addition of 4 g of sodium chloride, no addition of methanol as organic modifier, and 30 min ultrasonic desorption in acetonitrile. Recoveries ranged from 38 % to 58 % (RSD < 15 %, n = 6). Validated limits of quantification in matrix were between 1.6 ngL−1 and 548.8 ngL−1, depending on the compound. |
topic |
Fast gas chromatography‑mass spectrometry water pesticides electron ionization SBSE |
url |
https://acta.mendelu.cz/65/5/1595/ |
work_keys_str_mv |
AT andreapurdesova determinationofselectedpesticideresiduesinriverwaterusingsbsetechnique |
_version_ |
1725737401250217984 |