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In-situ tailoring of the electrocatalytic properties of screen-printed graphite electrodes with sparked generated molybdenum nanoparticles for the simultaneous voltammetric determination of sunset yellow and tartrazine

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F20%3A00115122" target="_blank" >RIV/00216224:14310/20:00115122 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://www.sciencedirect.com/science/article/pii/S0925400519314674" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0925400519314674</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.snb.2019.127268" target="_blank" >10.1016/j.snb.2019.127268</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    In-situ tailoring of the electrocatalytic properties of screen-printed graphite electrodes with sparked generated molybdenum nanoparticles for the simultaneous voltammetric determination of sunset yellow and tartrazine

  • Popis výsledku v původním jazyce

    This work describes the development of a “green” electrocatalytic surface based on molybdenum-sparked screen-printed graphite electrodes (sparked Mo-SPEs) for the voltammetric determination of azo synthetic colorants. Sparked Mo-SPEs were produced by an in-situ, liquid-free metal-to-SPE electric discharge approach at 1.2 kV under atmospheric conditions. Morphological studies with scanning electron microscopy and energy dispersive X-ray spectroscopy revealed the formation of Mo nanoparticles that have been evenly distributed over the entire surface of the electrodes. X-ray photoelectron spectroscopy showed that the atomic percentage of Mo over the electrode surface is only 0.5 ± 0.1% in the form of metallic Mo (25.3%) and Mo(VI) (74.7%). In 0.1 M acetate buffer solution, pH 5 sparked Mo-SPEs exhibited well-defined oxidation peaks at 0.730 V for sunset yellow (SY) and 0.973 V for tartrazine (TAR) versus Ag/AgCl/3 M KCl. Sparked Mo-SPE demonstrated remarkably increased responses compared with plain or electrodeposited MoxOy modified-graphite SPEs and enabled the simultaneous determination of the targets in the nano molar range. Under selected experimental variables a linear calibration curve over the concentration range from 5 to 250 nM SY/TAR was constructed. The limits of detection (S/N 3) were 2 nM. The response of Mo-SPE in the presence of other azo colorants was also investigated. The developed electrodes were successfully applied to the determination of SY and TAR in real-world samples. The accuracy of the method was established by recovery studies. Recovery was between 94–109%.

  • Název v anglickém jazyce

    In-situ tailoring of the electrocatalytic properties of screen-printed graphite electrodes with sparked generated molybdenum nanoparticles for the simultaneous voltammetric determination of sunset yellow and tartrazine

  • Popis výsledku anglicky

    This work describes the development of a “green” electrocatalytic surface based on molybdenum-sparked screen-printed graphite electrodes (sparked Mo-SPEs) for the voltammetric determination of azo synthetic colorants. Sparked Mo-SPEs were produced by an in-situ, liquid-free metal-to-SPE electric discharge approach at 1.2 kV under atmospheric conditions. Morphological studies with scanning electron microscopy and energy dispersive X-ray spectroscopy revealed the formation of Mo nanoparticles that have been evenly distributed over the entire surface of the electrodes. X-ray photoelectron spectroscopy showed that the atomic percentage of Mo over the electrode surface is only 0.5 ± 0.1% in the form of metallic Mo (25.3%) and Mo(VI) (74.7%). In 0.1 M acetate buffer solution, pH 5 sparked Mo-SPEs exhibited well-defined oxidation peaks at 0.730 V for sunset yellow (SY) and 0.973 V for tartrazine (TAR) versus Ag/AgCl/3 M KCl. Sparked Mo-SPE demonstrated remarkably increased responses compared with plain or electrodeposited MoxOy modified-graphite SPEs and enabled the simultaneous determination of the targets in the nano molar range. Under selected experimental variables a linear calibration curve over the concentration range from 5 to 250 nM SY/TAR was constructed. The limits of detection (S/N 3) were 2 nM. The response of Mo-SPE in the presence of other azo colorants was also investigated. The developed electrodes were successfully applied to the determination of SY and TAR in real-world samples. The accuracy of the method was established by recovery studies. Recovery was between 94–109%.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2020

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Sensors and Actuators B: Chemical

  • ISSN

    0925-4005

  • e-ISSN

  • Svazek periodika

    304

  • Číslo periodika v rámci svazku

    February 1

  • Stát vydavatele periodika

    CH - Švýcarská konfederace

  • Počet stran výsledku

    8

  • Strana od-do

    1-8

  • Kód UT WoS článku

    000500702500087

  • EID výsledku v databázi Scopus

    2-s2.0-85074225222