Svancara, Ivan

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  • Svancara, Ivan (2)
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Author's Bibliography

Voltammetric Determination of the Herbicide Linuron Using a Tricresyl Phosphate-Based Carbon Paste Electrode

Đorđević, Jelena S.; Papp, Zsigmond; Guzsvany, Valeria; Svancara, Ivan; Trtić-Petrović, Tatjana M.; Purenović, Milovan M.; Vytras, Karel

(2012)

TY  - JOUR
AU  - Đorđević, Jelena S.
AU  - Papp, Zsigmond
AU  - Guzsvany, Valeria
AU  - Svancara, Ivan
AU  - Trtić-Petrović, Tatjana M.
AU  - Purenović, Milovan M.
AU  - Vytras, Karel
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4660
AB  - This paper summarises the results of voltammetric studies on the herbicide 3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea (Linuron), using a carbon paste electrode containing tricresyl phosphate (TCP-CPE) as liquid binder. The principal experimental conditions, such as the pH effect, investigated in Britton-Robinson buffer solutions (pH 2.0-7.0), the peak characteristics for the analyte of interest, or instrumental parameters for the differential pulse voltammetric mode were optimized for the method. As found out, the best electroanalytical performance of the TCP-CPE was achieved at pH 2.0, whereby the oxidation peak of Linuron appeared at ca. + 1.3 V vs. SCE. The analytical procedure developed offers good linearity in the concentration range of 1.25-44.20 mu g mL(-1) (1.77 x 10(-4)-5.05 x 10(-6) mol L-1), showing-for the first time-the applicability of the TCP-CPE for anodic oxidations in direct voltammetry (without accumulation). The method was then verified by determining Linuron in a spiked river water sample and a commercial formulation and the results obtained agreed well with those obtained by the reference HPLC/UV determination.
T2  - Sensors
T1  - Voltammetric Determination of the Herbicide Linuron Using a Tricresyl Phosphate-Based Carbon Paste Electrode
VL  - 12
IS  - 1
SP  - 148
EP  - 161
DO  - 10.3390/s120100148
ER  - 
@article{
author = "Đorđević, Jelena S. and Papp, Zsigmond and Guzsvany, Valeria and Svancara, Ivan and Trtić-Petrović, Tatjana M. and Purenović, Milovan M. and Vytras, Karel",
year = "2012",
abstract = "This paper summarises the results of voltammetric studies on the herbicide 3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea (Linuron), using a carbon paste electrode containing tricresyl phosphate (TCP-CPE) as liquid binder. The principal experimental conditions, such as the pH effect, investigated in Britton-Robinson buffer solutions (pH 2.0-7.0), the peak characteristics for the analyte of interest, or instrumental parameters for the differential pulse voltammetric mode were optimized for the method. As found out, the best electroanalytical performance of the TCP-CPE was achieved at pH 2.0, whereby the oxidation peak of Linuron appeared at ca. + 1.3 V vs. SCE. The analytical procedure developed offers good linearity in the concentration range of 1.25-44.20 mu g mL(-1) (1.77 x 10(-4)-5.05 x 10(-6) mol L-1), showing-for the first time-the applicability of the TCP-CPE for anodic oxidations in direct voltammetry (without accumulation). The method was then verified by determining Linuron in a spiked river water sample and a commercial formulation and the results obtained agreed well with those obtained by the reference HPLC/UV determination.",
journal = "Sensors",
title = "Voltammetric Determination of the Herbicide Linuron Using a Tricresyl Phosphate-Based Carbon Paste Electrode",
volume = "12",
number = "1",
pages = "148-161",
doi = "10.3390/s120100148"
}
Đorđević, J. S., Papp, Z., Guzsvany, V., Svancara, I., Trtić-Petrović, T. M., Purenović, M. M.,& Vytras, K.. (2012). Voltammetric Determination of the Herbicide Linuron Using a Tricresyl Phosphate-Based Carbon Paste Electrode. in Sensors, 12(1), 148-161.
https://doi.org/10.3390/s120100148
Đorđević JS, Papp Z, Guzsvany V, Svancara I, Trtić-Petrović TM, Purenović MM, Vytras K. Voltammetric Determination of the Herbicide Linuron Using a Tricresyl Phosphate-Based Carbon Paste Electrode. in Sensors. 2012;12(1):148-161.
doi:10.3390/s120100148 .
Đorđević, Jelena S., Papp, Zsigmond, Guzsvany, Valeria, Svancara, Ivan, Trtić-Petrović, Tatjana M., Purenović, Milovan M., Vytras, Karel, "Voltammetric Determination of the Herbicide Linuron Using a Tricresyl Phosphate-Based Carbon Paste Electrode" in Sensors, 12, no. 1 (2012):148-161,
https://doi.org/10.3390/s120100148 . .
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Trace Determination of Carbendazim Fungicide Using Adsorptive Stripping Voltammetry with a Carbon Paste Electrode Containing Tricresyl Phosphate

Ashrafi, Amir M.; Đorđević, Jelena S.; Guzsvany, Valeria; Svancara, Ivan; Trtić-Petrović, Tatjana M.; Purenović, Milovan M.; Vytras, Karel

(2012)

TY  - JOUR
AU  - Ashrafi, Amir M.
AU  - Đorđević, Jelena S.
AU  - Guzsvany, Valeria
AU  - Svancara, Ivan
AU  - Trtić-Petrović, Tatjana M.
AU  - Purenović, Milovan M.
AU  - Vytras, Karel
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/5235
AB  - In this study, a carbon paste electrode based on tricresyl phosphate (TCP-CPE) as a binder has been applied to the voltammetric characterization and determination of Carbendazim fungicide (methyl-1H-benzimidazol-2-yl-carbamate, MBC). The pH effect (in Britton-Robinson buffers, pH 2.0-8.0), as well as the presence of 2-hydroxypropyl-beta-cyclodextrin (HPCD) on the electrochemical behavior of MBC were investigated. In the potential range of interest, the oxidation signal was observed with the overall shape strongly dependent upon pH and exhibiting the most favorable signal-to-noise ratio in mild acidic solutions (pH 4.0). This has indicated that also protons are involved in the electrode transformation of MBC. Furthermore, it was confirmed that addition of 3.6.10(-5) mol L-1 HPCD significantly enhanced the sensitivity towards the target analyte. The experimental conditions optimised for the determination of MBC in the differential pulse adsorptive stripping voltammetric mode (DPAdSV) were as follows: initial potential, -0.10 V vs. Ag/AgCl; final potential, +1.30 V; accumulation potential, -0.35 V; accumulation time, 120 s, and the scan rate, 100 mV s(-1). The method developed offers linearity in the concentration range of 5.0 .10(-7) - 1.0.10(-5) mol L-1 MBC, with r = 0.995 and the limit of detection of about 3.0.10(-7) mol L-1. In a model sample of spiked river water, the recovery rate achieved was 101.9 % (at the concentrations from 1.0.10(-6) to 3.0.10(-6) mol L-1 MBC), suggesting one that the procedure can be applied in analysis of real samples.
T2  - International Journal of Electrochemical Science
T1  - Trace Determination of Carbendazim Fungicide Using Adsorptive Stripping Voltammetry with a Carbon Paste Electrode Containing Tricresyl Phosphate
VL  - 7
IS  - 10
SP  - 9717
EP  - 9731
UR  - https://hdl.handle.net/21.15107/rcub_vinar_5235
ER  - 
@article{
author = "Ashrafi, Amir M. and Đorđević, Jelena S. and Guzsvany, Valeria and Svancara, Ivan and Trtić-Petrović, Tatjana M. and Purenović, Milovan M. and Vytras, Karel",
year = "2012",
abstract = "In this study, a carbon paste electrode based on tricresyl phosphate (TCP-CPE) as a binder has been applied to the voltammetric characterization and determination of Carbendazim fungicide (methyl-1H-benzimidazol-2-yl-carbamate, MBC). The pH effect (in Britton-Robinson buffers, pH 2.0-8.0), as well as the presence of 2-hydroxypropyl-beta-cyclodextrin (HPCD) on the electrochemical behavior of MBC were investigated. In the potential range of interest, the oxidation signal was observed with the overall shape strongly dependent upon pH and exhibiting the most favorable signal-to-noise ratio in mild acidic solutions (pH 4.0). This has indicated that also protons are involved in the electrode transformation of MBC. Furthermore, it was confirmed that addition of 3.6.10(-5) mol L-1 HPCD significantly enhanced the sensitivity towards the target analyte. The experimental conditions optimised for the determination of MBC in the differential pulse adsorptive stripping voltammetric mode (DPAdSV) were as follows: initial potential, -0.10 V vs. Ag/AgCl; final potential, +1.30 V; accumulation potential, -0.35 V; accumulation time, 120 s, and the scan rate, 100 mV s(-1). The method developed offers linearity in the concentration range of 5.0 .10(-7) - 1.0.10(-5) mol L-1 MBC, with r = 0.995 and the limit of detection of about 3.0.10(-7) mol L-1. In a model sample of spiked river water, the recovery rate achieved was 101.9 % (at the concentrations from 1.0.10(-6) to 3.0.10(-6) mol L-1 MBC), suggesting one that the procedure can be applied in analysis of real samples.",
journal = "International Journal of Electrochemical Science",
title = "Trace Determination of Carbendazim Fungicide Using Adsorptive Stripping Voltammetry with a Carbon Paste Electrode Containing Tricresyl Phosphate",
volume = "7",
number = "10",
pages = "9717-9731",
url = "https://hdl.handle.net/21.15107/rcub_vinar_5235"
}
Ashrafi, A. M., Đorđević, J. S., Guzsvany, V., Svancara, I., Trtić-Petrović, T. M., Purenović, M. M.,& Vytras, K.. (2012). Trace Determination of Carbendazim Fungicide Using Adsorptive Stripping Voltammetry with a Carbon Paste Electrode Containing Tricresyl Phosphate. in International Journal of Electrochemical Science, 7(10), 9717-9731.
https://hdl.handle.net/21.15107/rcub_vinar_5235
Ashrafi AM, Đorđević JS, Guzsvany V, Svancara I, Trtić-Petrović TM, Purenović MM, Vytras K. Trace Determination of Carbendazim Fungicide Using Adsorptive Stripping Voltammetry with a Carbon Paste Electrode Containing Tricresyl Phosphate. in International Journal of Electrochemical Science. 2012;7(10):9717-9731.
https://hdl.handle.net/21.15107/rcub_vinar_5235 .
Ashrafi, Amir M., Đorđević, Jelena S., Guzsvany, Valeria, Svancara, Ivan, Trtić-Petrović, Tatjana M., Purenović, Milovan M., Vytras, Karel, "Trace Determination of Carbendazim Fungicide Using Adsorptive Stripping Voltammetry with a Carbon Paste Electrode Containing Tricresyl Phosphate" in International Journal of Electrochemical Science, 7, no. 10 (2012):9717-9731,
https://hdl.handle.net/21.15107/rcub_vinar_5235 .
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