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Improved electroanalytical characteristics for flumetralin determination in the presence of surface active compound

ABSTRACT: The use of square wave voltammetry (SWV) and square wave adsorptive stripping voltammetry (SWAdSV) in conjunction with a cyclic renewable silver amalgam film electrode for the determination of flumetralin is presented. Poor separation of two overlapped reduction peaks is significantly impr...

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Detalles Bibliográficos
Autores principales: Guziejewski, Dariusz, Smarzewska, Sylwia, Metelka, Radovan, Nosal-Wiercińska, Agnieszka, Ciesielski, Witold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346150/
https://www.ncbi.nlm.nih.gov/pubmed/28344364
http://dx.doi.org/10.1007/s00706-017-1918-8
Descripción
Sumario:ABSTRACT: The use of square wave voltammetry (SWV) and square wave adsorptive stripping voltammetry (SWAdSV) in conjunction with a cyclic renewable silver amalgam film electrode for the determination of flumetralin is presented. Poor separation of two overlapped reduction peaks is significantly improved when hexadecyltrimethylammonium bromide is used as a component of the supporting electrolyte solution (together with BR buffer pH 9.5). The SW technique parameters were investigated and found optimal as follows: frequency 50 Hz, amplitude 40 mV, and step potential 5 mV. Accumulation time and potential were studied to select the optimal conditions in adsorptive voltammetry. The analytical curve was linear for the flumetralin concentration range from 1.0 × 10(−6) to 1.0 × 10(−5) mol dm(−3) and from 5.0 × 10(−9) to 1.0 × 10(−7) mol dm(−3) for SWV and SWAdSV, respectively. Detection limit of 6.5 × 10(−10) mol dm(−3) was calculated for accumulation time 60 s at −0.2 V. The repeatability of the method was determined at a flumetralin concentration level equal to 5.0 × 10(−9) mol dm(−3) and expressed as %RSD = 5.0% (n = 6). The proposed method was applied and validated successfully by studying the recovery of herbicide content in spiked environmental samples. GRAPHICAL ABSTRACT: [Image: see text]