Application of a fully integrated photodegradation-detection flow-batch analysis system with an on-line preconcentration step for the determination of metsulfuron methyl in water samples
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25127589
DOI
10.1016/j.talanta.2014.05.024
PII: S0039-9140(14)00408-1
Knihovny.cz E-zdroje
- Klíčová slova
- Flow-batch analysis, Fluorescence, Metsulfuron methyl, On-line solid phase extraction, Photoinduced degradation,
- MeSH
- arylsulfonany analýza MeSH
- extrakce na pevné fázi MeSH
- fluorescenční spektrometrie MeSH
- fotochemie metody MeSH
- fotolýza MeSH
- herbicidy analýza MeSH
- kalibrace MeSH
- koncentrace vodíkových iontů MeSH
- látky znečišťující vodu analýza MeSH
- limita detekce MeSH
- reprodukovatelnost výsledků MeSH
- sulfonylmočovinové sloučeniny analýza MeSH
- světlo MeSH
- technologie zelené chemie MeSH
- voda chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- arylsulfonany MeSH
- herbicidy MeSH
- látky znečišťující vodu MeSH
- metsulfuron methyl MeSH Prohlížeč
- sulfonylmočovinové sloučeniny MeSH
- voda MeSH
This work presents the development of a fully automated flow-batch analysis (FBA) system as a new approach for on-line preconcentration, photodegradation and fluorescence detection in a lab-constructed mixing chamber that was designed to perform these processes without sample dispersion. The system positions the mixing chamber into the detection system and varies the instrumental parameters according to the required photodegradation conditions. The developed FBA system is simple and easily coupled with any sample pretreatment without altering the configuration. This FBA system was implemented to photodegrade and determine the fluorescence of the degradation products of metsulfuron methyl (MSM), a naturally non-fluorescent herbicide of the sulfonylurea׳s family. An on-line solid phase extraction (SPE) and clean up procedure using a C18 minicolumn was coupled to the photodegradation-detection mixing chamber (PDMC) that was located in the spectrofluorometer. An enrichment factor of 27 was achieved. Photodegradation conditions have been optimized by considering the influence of the elution solvent on both the formation of the photoproduct and on the fluorescence signal. Under optimal conditions, the calibration for the MSM determination was linear over the range of 1.00-7.20 µg L(-1). The limit of detection (LOD) was 0.28 µg L(-1); the relative standard deviation was 2.0% and the sample throughput for the entire process was 3h(-1). The proposed method was applied to real water samples from the Bahía Blanca׳s agricultural region (Bahía Blanca, Buenos Aires, Argentina). This method obtained satisfactory recoveries with a range of 94.7-109.8%.
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