Bestimmung von Pflanzenbehandlungsmitteln in Wasser durch Online-Fest-Flüssig-Extraktion und HPLC-DAD
Autor: | R. Reupert, R. Schuster, G. Brausen |
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Rok vydání: | 1998 |
Předmět: | |
Zdroj: | Acta hydrochimica et hydrobiologica. 26:318-329 |
ISSN: | 1521-401X 0323-4320 |
DOI: | 10.1002/(sici)1521-401x(199811)26:6<318::aid-aheh318>3.0.co;2-5 |
Popis: | This paper describes an HPLC on-line procedure for the determination of 29 relevant pesticides in water by diode-array detection using a compact HPLC-system with integrated column-switching. The sample - 5 mL - is injected with a large volume injection system on a pre-column cartridge (RP-C18). Enriched compounds are eluted in front-flush mode by column-switching to a microbore column and separated with a gradient water/acetonitrile. During desorption the pre-column cartridge is heated at 80°C resulting in a comparable efficiency to the separation with direct injection. The procedure is fully automated for continuous monitoring of drinking-, ground-, and surface water with low contamination levels. Sample preparation is limited to a filtration step with an anion-exchange membrane filter to reduce natural contaminations e.g. humic acids simultaneously. For a concentration of 50 ng/L, the signal to noise ratio varies from 3:1 (Ethidimuron) up to 25:1 (Chloridazon). The standard deviations compare to the standardized HPLC-method DIN EN ISO 11369; the recovery rates are 100% and reproducible. The method was successfully tested on ruggedness with several sequences from a monitoring program. The pre-column cartridge needs replacement after 100 sample injections. Finally, this method was coupled with a benchtop mass-spectrometer (electrospray mode) without changing the chromatographic conditions. With selected ion monitoring (SIM) selectivity and detection sensitivity could be improved considerably compared to DAD-detection. |
Databáze: | OpenAIRE |
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