New method for the determination of carbamate and pyrethroid insecticides in water samples using on-line SPE fused core column chromatography
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25127636
DOI
10.1016/j.talanta.2014.06.037
PII: S0039-9140(14)00493-7
Knihovny.cz E-resources
- Keywords
- Carbamates, Chromatography, Large volume sample injection, On-line solid phase extraction (on-line SPE), Pyrethroids, Surface water,
- MeSH
- Water Pollutants, Chemical analysis MeSH
- Chromatography, Liquid MeSH
- Solid Phase Extraction methods MeSH
- Insecticides analysis MeSH
- Lakes MeSH
- Carbamates analysis MeSH
- Environmental Monitoring methods MeSH
- Online Systems MeSH
- Organic Chemicals analysis MeSH
- Pyrethrins analysis MeSH
- Rivers MeSH
- Reproducibility of Results MeSH
- Spectrophotometry, Ultraviolet MeSH
- Water chemistry MeSH
- Chromatography, High Pressure Liquid methods MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
- Names of Substances
- Water Pollutants, Chemical MeSH
- Insecticides MeSH
- Carbamates MeSH
- Organic Chemicals MeSH
- Pyrethrins MeSH
- Water MeSH
A new HPLC column-switching method using large volume sample injection and fused-core columns for on-line solid phase extraction have been developed for the determination of the following carbamates and pyrethroids: aldicarb, carbaryl, pirimicarb, carbofuran, kadethrin, flumethrin, fenpropathrin, fenoxycarb, tau-fluvalinate and fenvalerate, in surface water samples. Sudan I was used as internal standard. The proposed method was performed using 100 µl sample injection followed by an on-line solid phase extraction procedure and finally the compounds were identified and quantified by liquid chromatography with ultraviolet detection. The separation was carried out on C-18 reversed phase column based on fused-core particle technology. The influence of the injected sample volume, the variables affecting to SPE process and the conditions for the separation on an analytical column, were studied and optimized. The limits of detection ranged from 5.5 to 8.9 µg L(-1), and limits of quantification from 18.4 to 29.7 µg L(-1), while inter- and intra-day variability was under 15%. This new analytical procedure was satisfactorily applied for the determination of these organic pollutants in surface water samples located in Czech Republic. Concentration levels were found for some of these pollutants up to 26.11 µg L(-1) in the river Elbe and up to 34.53 µg L(-1) in the closed lakes samples.
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