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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2017
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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 |
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author | Guziejewski, Dariusz Smarzewska, Sylwia Metelka, Radovan Nosal-Wiercińska, Agnieszka Ciesielski, Witold |
author_facet | Guziejewski, Dariusz Smarzewska, Sylwia Metelka, Radovan Nosal-Wiercińska, Agnieszka Ciesielski, Witold |
author_sort | Guziejewski, Dariusz |
collection | PubMed |
description | 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] |
format | Online Article Text |
id | pubmed-5346150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-53461502017-03-22 Improved electroanalytical characteristics for flumetralin determination in the presence of surface active compound Guziejewski, Dariusz Smarzewska, Sylwia Metelka, Radovan Nosal-Wiercińska, Agnieszka Ciesielski, Witold Monatsh Chem Original Paper 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] Springer Vienna 2017-02-08 2017 /pmc/articles/PMC5346150/ /pubmed/28344364 http://dx.doi.org/10.1007/s00706-017-1918-8 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Paper Guziejewski, Dariusz Smarzewska, Sylwia Metelka, Radovan Nosal-Wiercińska, Agnieszka Ciesielski, Witold Improved electroanalytical characteristics for flumetralin determination in the presence of surface active compound |
title | Improved electroanalytical characteristics for flumetralin determination in the presence of surface active compound |
title_full | Improved electroanalytical characteristics for flumetralin determination in the presence of surface active compound |
title_fullStr | Improved electroanalytical characteristics for flumetralin determination in the presence of surface active compound |
title_full_unstemmed | Improved electroanalytical characteristics for flumetralin determination in the presence of surface active compound |
title_short | Improved electroanalytical characteristics for flumetralin determination in the presence of surface active compound |
title_sort | improved electroanalytical characteristics for flumetralin determination in the presence of surface active compound |
topic | Original Paper |
url | 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 |
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