This article describes a new method for the determination of ultra trace levels of 12 N-methylcarbamates in drinking water via micellar electrokinetic Ž . chromatography MEKC . Two steps were employed to enhance the detection sensitivity. The sample was first preconcentrated by C bonded SPE cartridg
Separation and determination of pesticides by capillary electrophoresis. I. Rapid separation of fifteen N-methylcarbamate insecticides via micellar electrokinetic chromatography
✍ Scribed by Y.S. Wu; H.K. Lee; S.F.Y. Li
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 191 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1040-7685
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✦ Synopsis
In this article, micellar electrokinetic chromatography MEKC separation of 15 N-methylcarbamate insecticides with a wide span of hydrophobicity was studied. Influences of various buffer parameters such as sodium dodecyl sulfate Ž . Ž . SDS concentration, ionic strength, and modifiers urea, cyclodextrins on separation selectivity and analysis time were investigated. Under the optimized running Ž condition 40 mM phosphate with 60 mM SDS and 23 mM hydroxypropyl--cyclo-. dextrin, pH 7, voltage 18 kV , satisfactory separation of all 15 analytes was achieved in less than 14 min. Using this new method, residues of carbaryl and its metabolite in a paddy water sample were successfully determined. This new alternative for the separation of N-methylcarbamates is superior to conventional Ž . reversed-phase high-performance liquid chromatography HPLC approaches in terms of speed of separation and flexibility of selectivity manipulation.
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