An integrated on-line method for the preconcentration and simultaneous determination of metsulfuron methyl and chlorsulfuron using oxidized carbon nanotubes and second order fluorescent data
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11160%2F16%3A10326189" target="_blank" >RIV/00216208:11160/16:10326189 - isvavai.cz</a>
Výsledek na webu
<a href="http://www.sciencedirect.com/science/article/pii/S0026265X16300923" target="_blank" >http://www.sciencedirect.com/science/article/pii/S0026265X16300923</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.microc.2016.06.011" target="_blank" >10.1016/j.microc.2016.06.011</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
An integrated on-line method for the preconcentration and simultaneous determination of metsulfuron methyl and chlorsulfuron using oxidized carbon nanotubes and second order fluorescent data
Popis výsledku v původním jazyce
Trace amounts of two sulfonylurea herbicides widely used for crops protection, metsulfuron methyl (MSM) and chlorsulfuron (CSF) were simultaneously determined taking into account the different kinetic photodegradation behavior of their photoproducts in alkaline medium. As the analytes are present at trace concentration levels, a preconcentration by sorption on a mini-column packed with oxidized multiwall carbon nanotubes (ox-MWCNTs) at pH 3.0 was performed. The retained analytes were removed from the ox-MWCNTs mini-column with a mixture of ACN contained 10% (v/v) of NaOH pH 12.5. A total enrichment factor of 26-fold for a 14.50 mL sample volume was obtained. The eluate was photodegraded by UV radiation during 126 s and the fluorescent spectra corresponding to the analytes photoproducts were registered overtime between 300 and 500 nm. The kinetic second order data were analyzed by unfolded-partial least squares-residual bilinearization (U-PLS/RBL) and multidimensional-partial least squares-residual bilinearization (N-PLS/RBL) algorithms. The relative error of prediction (REP %) for N-PLS/RBL was 7.73% for MSM and 6.37% for CSF. In the case of U-PLS/RBL, this statistical parameter was 7.75% for MSM and 7.23% for CSF, respectively. The limits of detection (LOD) were 0.19 mu g L-1 for MSM and 1.14 mu g L-1 for CSF using N-PLS/RBL and 0.21 mu g L-1 for MSM and 1.03 mu g L-1 for CSF when U-PLS/RBL was applied. The entire procedure was performed in an on-line integrated fully automated flow system coupled to a low mercury UV lamp (15 W, 254 nm) and a spectrofluorometer. In this manner, the preconcentration, photodegradation and detection steps were performed in a reproducible way. After optimization, the method was successfully applied to the analysis of real water samples obtained in the south part of Buenos Aires province and used for irrigation and consumption.
Název v anglickém jazyce
An integrated on-line method for the preconcentration and simultaneous determination of metsulfuron methyl and chlorsulfuron using oxidized carbon nanotubes and second order fluorescent data
Popis výsledku anglicky
Trace amounts of two sulfonylurea herbicides widely used for crops protection, metsulfuron methyl (MSM) and chlorsulfuron (CSF) were simultaneously determined taking into account the different kinetic photodegradation behavior of their photoproducts in alkaline medium. As the analytes are present at trace concentration levels, a preconcentration by sorption on a mini-column packed with oxidized multiwall carbon nanotubes (ox-MWCNTs) at pH 3.0 was performed. The retained analytes were removed from the ox-MWCNTs mini-column with a mixture of ACN contained 10% (v/v) of NaOH pH 12.5. A total enrichment factor of 26-fold for a 14.50 mL sample volume was obtained. The eluate was photodegraded by UV radiation during 126 s and the fluorescent spectra corresponding to the analytes photoproducts were registered overtime between 300 and 500 nm. The kinetic second order data were analyzed by unfolded-partial least squares-residual bilinearization (U-PLS/RBL) and multidimensional-partial least squares-residual bilinearization (N-PLS/RBL) algorithms. The relative error of prediction (REP %) for N-PLS/RBL was 7.73% for MSM and 6.37% for CSF. In the case of U-PLS/RBL, this statistical parameter was 7.75% for MSM and 7.23% for CSF, respectively. The limits of detection (LOD) were 0.19 mu g L-1 for MSM and 1.14 mu g L-1 for CSF using N-PLS/RBL and 0.21 mu g L-1 for MSM and 1.03 mu g L-1 for CSF when U-PLS/RBL was applied. The entire procedure was performed in an on-line integrated fully automated flow system coupled to a low mercury UV lamp (15 W, 254 nm) and a spectrofluorometer. In this manner, the preconcentration, photodegradation and detection steps were performed in a reproducible way. After optimization, the method was successfully applied to the analysis of real water samples obtained in the south part of Buenos Aires province and used for irrigation and consumption.
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
CB - Analytická chemie, separace
OECD FORD obor
—
Návaznosti výsledku
Projekt
<a href="/cs/project/7AMB14AR029" target="_blank" >7AMB14AR029: Využití moderních průtokových metod pro stanovení biologicky aktivních látek v komplexních matricích</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2016
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Microchemical Journal
ISSN
0026-265X
e-ISSN
—
Svazek periodika
129
Číslo periodika v rámci svazku
November
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
8
Strana od-do
90-97
Kód UT WoS článku
000382595300014
EID výsledku v databázi Scopus
2-s2.0-84974856589