Dataset for electrochemical oxidation of triticonazole published in Electrochemical Oxidation of Triticonazole on Boron-Doped Diamond-Based Electrodes for Analysis of Real Matrices
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F26%3A00647164" target="_blank" >RIV/61388955:_____/26:00647164 - isvavai.cz</a>
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Dataset for electrochemical oxidation of triticonazole published in Electrochemical Oxidation of Triticonazole on Boron-Doped Diamond-Based Electrodes for Analysis of Real Matrices
Popis výsledku v původním jazyce
The voltammetric behavior of the triazole fungicide triticonazole (TTC) was investigated for the first time using a boron-doped diamond electrode (BDDE). TTC showed an irreversible oxidation peak at +1.5 V, a weak second oxidation near +2.0 V, and a reduction peak around 0 V (vs. Ag/AgCl/KCl, sat.). The oxidation mechanism was proposed based on electrochemical experiments, theoretical calculations, and LC/MS analysis after exhaustive electrolysis. A square-wave voltammetric method was developed with a detection limit of 0.125 µmol L⁻¹ and a linear range of 0.5–20 µmol L⁻¹. For natural waters, solid-phase extraction preconcentration was applied. The method was successfully transferred to screen-printed BDDE sensors, extending the linear range to 0.25–60 µmol L⁻¹ and improving sensitivity by 1.68–1.85×.
Název v anglickém jazyce
Dataset for electrochemical oxidation of triticonazole published in Electrochemical Oxidation of Triticonazole on Boron-Doped Diamond-Based Electrodes for Analysis of Real Matrices
Popis výsledku anglicky
The voltammetric behavior of the triazole fungicide triticonazole (TTC) was investigated for the first time using a boron-doped diamond electrode (BDDE). TTC showed an irreversible oxidation peak at +1.5 V, a weak second oxidation near +2.0 V, and a reduction peak around 0 V (vs. Ag/AgCl/KCl, sat.). The oxidation mechanism was proposed based on electrochemical experiments, theoretical calculations, and LC/MS analysis after exhaustive electrolysis. A square-wave voltammetric method was developed with a detection limit of 0.125 µmol L⁻¹ and a linear range of 0.5–20 µmol L⁻¹. For natural waters, solid-phase extraction preconcentration was applied. The method was successfully transferred to screen-printed BDDE sensors, extending the linear range to 0.25–60 µmol L⁻¹ and improving sensitivity by 1.68–1.85×.
Klasifikace
Druh
X - Nezařazeno
CEP obor
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OECD FORD obor
10403 - Physical chemistry
Návaznosti výsledku
Projekt
<a href="/cs/project/EH22_008%2F0004558" target="_blank" >EH22_008/0004558: Pokročilé víceškálové materiály pro nosné klíčové technologie</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2026
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů