Voltammetric Behaviour and Determination of 8-Hydroxyquinoline Using a Glassy Carbon Paste Electrode and the Theoretical Study of its Electrochemical Oxidation Mechanism
Нема приказа
Аутори
Stevic, Milica C.Ignjatovic, Ljubisa M.
Ćirić-Marjanović, Gordana
Stanišić, Svetlana M.
Stanković, Dalibor
Zima, Jiri
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
The 8-Hydroxyquinoline (8HQ) oxidation process has been investigated by Cyclic Voltammetry using a Glassy Carbon Paste Electrode (GCPE) as a working electrode. The theoretical study of the mechanism of electrochemical oxidation of 8HQ has been based on the AM1 semi-empirical quantum chemical computations of the heats of formation of the reaction intermediates, taking into account the influence of pH and solvation effects. We proposed that a two-electron irreversible process, controlled by diffusion of electroactive species, is responsible for an oxidation peak of 8HQ that appears in all cyclic voltammograms recorded on a clean electrode in the solutions of pH in the range 2-12 with a supporting electrolyte of Britton-Robinson Buffer/methanol. A single-electron oxidation of 8HQ leads, depending on pH, to the formation of various free radical species that combine to make dimers which, after being oxidized once more, give quinonoid-type compounds. Recording continuous cyclic voltammograms... on the GCPE, pre-peaks appear as a consequence of dimer and quinonoid compounds formation. By applying Differential Pulse Voltammetry for 8HQ determination it was calculated that the limit of detection was 5.2x10(-8) mol/L. For more sensitive quantitative determination of the investigated substance Adsorptive Stripping Differential Pulse Voltammery can be used since it was found that after 300s-deposition time at 0.0 V vs. Saturated Calomel Electrode, a 2.1 times higher peak current than without deposition was obtained.
Кључне речи:
8-Hydroxyquinoline / Glassy Carbon Paste Electrode / Cyclic Voltammetry / Differential Pulse Voltammetry / Computational methodИзвор:
International Journal of Electrochemical Science, 2011, 6, 7, 2509-2525Издавач:
- Electrochemical Science Group, Belgrade
Финансирање / пројекти:
- Примена унапређених оксидационих процеса и наноструктурисаних оксидних материјала за уклањање загађивача из животне средине, развој и оптимизација инструменталних техника за праћење ефикасности (RS-MESTD-Basic Research (BR or ON)-172030)
- Електропроводни и редокс-активни полимери и олигомери: синтеза, структура, својства и примена (RS-MESTD-Basic Research (BR or ON)-172043)
Колекције
Институција/група
Inovacioni centar / Innovation CentreTY - JOUR AU - Stevic, Milica C. AU - Ignjatovic, Ljubisa M. AU - Ćirić-Marjanović, Gordana AU - Stanišić, Svetlana M. AU - Stanković, Dalibor AU - Zima, Jiri PY - 2011 UR - https://cherry.chem.bg.ac.rs/handle/123456789/1171 AB - The 8-Hydroxyquinoline (8HQ) oxidation process has been investigated by Cyclic Voltammetry using a Glassy Carbon Paste Electrode (GCPE) as a working electrode. The theoretical study of the mechanism of electrochemical oxidation of 8HQ has been based on the AM1 semi-empirical quantum chemical computations of the heats of formation of the reaction intermediates, taking into account the influence of pH and solvation effects. We proposed that a two-electron irreversible process, controlled by diffusion of electroactive species, is responsible for an oxidation peak of 8HQ that appears in all cyclic voltammograms recorded on a clean electrode in the solutions of pH in the range 2-12 with a supporting electrolyte of Britton-Robinson Buffer/methanol. A single-electron oxidation of 8HQ leads, depending on pH, to the formation of various free radical species that combine to make dimers which, after being oxidized once more, give quinonoid-type compounds. Recording continuous cyclic voltammograms on the GCPE, pre-peaks appear as a consequence of dimer and quinonoid compounds formation. By applying Differential Pulse Voltammetry for 8HQ determination it was calculated that the limit of detection was 5.2x10(-8) mol/L. For more sensitive quantitative determination of the investigated substance Adsorptive Stripping Differential Pulse Voltammery can be used since it was found that after 300s-deposition time at 0.0 V vs. Saturated Calomel Electrode, a 2.1 times higher peak current than without deposition was obtained. PB - Electrochemical Science Group, Belgrade T2 - International Journal of Electrochemical Science T1 - Voltammetric Behaviour and Determination of 8-Hydroxyquinoline Using a Glassy Carbon Paste Electrode and the Theoretical Study of its Electrochemical Oxidation Mechanism VL - 6 IS - 7 SP - 2509 EP - 2525 UR - https://hdl.handle.net/21.15107/rcub_cherry_1171 ER -
@article{ author = "Stevic, Milica C. and Ignjatovic, Ljubisa M. and Ćirić-Marjanović, Gordana and Stanišić, Svetlana M. and Stanković, Dalibor and Zima, Jiri", year = "2011", abstract = "The 8-Hydroxyquinoline (8HQ) oxidation process has been investigated by Cyclic Voltammetry using a Glassy Carbon Paste Electrode (GCPE) as a working electrode. The theoretical study of the mechanism of electrochemical oxidation of 8HQ has been based on the AM1 semi-empirical quantum chemical computations of the heats of formation of the reaction intermediates, taking into account the influence of pH and solvation effects. We proposed that a two-electron irreversible process, controlled by diffusion of electroactive species, is responsible for an oxidation peak of 8HQ that appears in all cyclic voltammograms recorded on a clean electrode in the solutions of pH in the range 2-12 with a supporting electrolyte of Britton-Robinson Buffer/methanol. A single-electron oxidation of 8HQ leads, depending on pH, to the formation of various free radical species that combine to make dimers which, after being oxidized once more, give quinonoid-type compounds. Recording continuous cyclic voltammograms on the GCPE, pre-peaks appear as a consequence of dimer and quinonoid compounds formation. By applying Differential Pulse Voltammetry for 8HQ determination it was calculated that the limit of detection was 5.2x10(-8) mol/L. For more sensitive quantitative determination of the investigated substance Adsorptive Stripping Differential Pulse Voltammery can be used since it was found that after 300s-deposition time at 0.0 V vs. Saturated Calomel Electrode, a 2.1 times higher peak current than without deposition was obtained.", publisher = "Electrochemical Science Group, Belgrade", journal = "International Journal of Electrochemical Science", title = "Voltammetric Behaviour and Determination of 8-Hydroxyquinoline Using a Glassy Carbon Paste Electrode and the Theoretical Study of its Electrochemical Oxidation Mechanism", volume = "6", number = "7", pages = "2509-2525", url = "https://hdl.handle.net/21.15107/rcub_cherry_1171" }
Stevic, M. C., Ignjatovic, L. M., Ćirić-Marjanović, G., Stanišić, S. M., Stanković, D.,& Zima, J.. (2011). Voltammetric Behaviour and Determination of 8-Hydroxyquinoline Using a Glassy Carbon Paste Electrode and the Theoretical Study of its Electrochemical Oxidation Mechanism. in International Journal of Electrochemical Science Electrochemical Science Group, Belgrade., 6(7), 2509-2525. https://hdl.handle.net/21.15107/rcub_cherry_1171
Stevic MC, Ignjatovic LM, Ćirić-Marjanović G, Stanišić SM, Stanković D, Zima J. Voltammetric Behaviour and Determination of 8-Hydroxyquinoline Using a Glassy Carbon Paste Electrode and the Theoretical Study of its Electrochemical Oxidation Mechanism. in International Journal of Electrochemical Science. 2011;6(7):2509-2525. https://hdl.handle.net/21.15107/rcub_cherry_1171 .
Stevic, Milica C., Ignjatovic, Ljubisa M., Ćirić-Marjanović, Gordana, Stanišić, Svetlana M., Stanković, Dalibor, Zima, Jiri, "Voltammetric Behaviour and Determination of 8-Hydroxyquinoline Using a Glassy Carbon Paste Electrode and the Theoretical Study of its Electrochemical Oxidation Mechanism" in International Journal of Electrochemical Science, 6, no. 7 (2011):2509-2525, https://hdl.handle.net/21.15107/rcub_cherry_1171 .