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Silver Amalgam Electrodes in Electroanalysis of Selected Agrochemicals
Daňhel, Aleš ; Barek, Jiří (advisor) ; Vytřas, Karel (referee) ; Ludvík, Jiří (referee)
4 ABSTRACT Development and testing of novel non-toxic electrode materials, detection arrangements and analytical methods applicable in determination of selected agrochemicals is the main aim of this Ph.D. Thesis. New working electrodes based on silver solid amalgam paste (AgSA-PE) with organic pasting liquid and other based on crystallic silver amalgam (CAgAE) were developed, their electrochemical behaviour investigated and further used in voltammetric determination of widespread and toxic environmental pollutant 4-nitrophenol (4-NP). This analyte could be determined by DPV at AgSA-PE with limit of detection (LD) 1×10í6 mol lí1 and using CAgAE with LD 4×10í7 mol lí1 , both in 0.2 mol lí1 acetate buffer pH 4.8. Attempts to decrease LDs by utilization of adsorptive stripping voltammetry were not successful in either case. Crystallic silver amalgam was also successfully used for construction of microcylindric flow-through cell and tested for amperometric determination of nitrophenol mixture in HPLC-ED system. Both novel electrodes were found to be suitable alternatives to toxic mercury electrodes and the CAgAE seems to be promising working electrode for flowing systems. Method for sample preparation and voltammetric determination of broad-spectrum herbicide Glyphosate in contaminated soil samples was also...
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Electrochemical sensor for ascorbic acid detection
Hlavička, Michal ; Kynclová, Hana (referee) ; Majzlíková, Petra (advisor)
This work deals with electrochemical detection of ascorbic acid using screen-printed three-electrode sensors. The work is divided into three parts, where the first describes the theory of thick-film technology, including the types and compositions of the pastes, fabrication and firing. The second part deals with the methods, measurement principles and the electrochemical detection of ascorbic acid. Experiments were done using screen-printed carbon electrodes in a solution of phosphate buffer and ascorbic acid. In conclusion the results are evaluated.
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Biosensors based on modified carbon nanotubes
Ferdusová, Helena ; Majzlík, Petr (referee) ; Hubálek, Jaromír (advisor)
The aim of this work is to describe biosensors for detection of substances in liquids using modified carbon nanotubes. This work reports on knowledge about nanotubes and electrochemical analysis methods which were used. The matter of direct electrochemical detection of insulin using CNTs modified thick layer planar carbon nanotubes is discussed. The elementary working electrodes were created by using of commercial carbon paste and were modified by thin film CNTs, CNTs/ruthenium oxide and CNTs/chitosan then. The best results of the insulin detection were achieved with the working electrodes modified by low concentration non-purified CNTs which had low elementary response in electrolyte and good response to increasing concentration of insulin in the concentration range from 0, 25 to 10 mol/L. The other modifications caused increasing of the electrode elementary response, but they did not significantly affect the detection.
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Testing of the electrochemical properties of flow-through diamond detector
Pecák, Jakub ; Dejmková, Hana (advisor) ; Vyskočil, Vlastimil (referee)
In the presented bachelor thesis, the functionality of a flow-through multitubular boron- doped diamond electrode (mtBDDE) was verified on two selected neurotransmitters, DA and NE, using the HPLC technique with isocratic elution. An aqueous solution of Britton-Robinson (B-R) buffer was chosen as the mobile phase and a Kinetex EVO C18 reverse column (150 x 4.6 mm) as the stationary phase. The flow rate of the mobile phase was set at 1 ml/min. For electrochemical detection, mtBDDE was used and UV detection at 280 nm was applied as an assistant to the main detector. The electrochemical response of the DA and NE solution (cΘ = 1.10-4 mol/dm3 ) was investigated in the form of hydrodynamic voltammograms over a potential range from 0.1 V to 1.3 V in different pH ranges of the mobile phase (2.5; 4.0; 6.0; 8.0 and 10.0). It was found that the potential wave shifts to lower potentials with increasing pH of the mobile phase, while the response of individual analytes does not change significantly with pH. Under optimal conditions, i.e., mobile phase B-R buffer at pH = 6 and a potential loaded on the mtBDDE of 0.6 V, the repeatability and reproducibility of the measurement results were verified. The electrode gave repeatable results (RSD < 4 %) comparable to the UV detector used (RSD ≤ 4 %) over the series of...
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Voltammetric and amperometric determination of homovanillic, vanillylmandelic, and 5-hydroxyindole-3-acetic acid
Němečková, Anna ; Barek, Jiří (advisor) ; Labuda, Ján (referee) ; Skopalová, Jana (referee)
Presented dissertation thesis is focused on the development of electrochemical methods for the determination of three important tumour biomarkers, namely homovanillic acid (HVA), vanillylmandelic acid (VMA), and 5-hydroxyindole-3-acetic acid (5-HIAA). First part of the study is focused on electrochemical behaviour of these analytes in batch arrangement using differential pulse voltammetry (DPV) at screen-printed carbon electrodes (SPCEs). It has been proved that presented method is sufficiently sensitive for monitoring above mentioned analytes. Moreover, it can be used for determination of HVA and VMA in mixture. Obtained limits of detection (LODs) were 0.24 µmol·L-1 for HVA, 0.06 µmol·L-1 for VMA, and 0.12 µmol·L-1 for 5-HIAA. The requirements to speed up the analysis and at the same time to reduce its price initialized our study of the determination of tested biomarkers in flow systems. Firstly, flow injection analysis with amperometric detection was investigated for the determination of all three biomarkers at the same SPCE, and then an analogous determination of structural more similar pair, HVA and VMA, was performed at a boron doped diamond electrode (BDDE). Obtained LODs of optimized methods were as follows: at SPCE 0.07 µmol·L-1 for HVA, 0.05 µmol·L-1 for VMA, and 0.03 µmol·L-1 for 5-HIAA,...
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