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Voltammetric determination of sulfathiazole on boron doped diamond electrode
Zich, Mikuláš ; Fischer, Jan (advisor) ; Schwarzová, Karolina (referee)
This bachelor thesis is dedicated to study of the electrochemically active substance sulfathiazole. Sulfathiazole is an antibacterial agent added to animal feed. As a result, it contaminates soil, water bodies and food. A boron-doped diamond electrode was chosen as the working electrode for voltammetric determination. First, the optimal pH for the study of sulfathiazole in the range of 2 to 12 by the technique differential pulse voltammetry was determined and the optimal pretreatment of the electrode before measurements. Subsequently, the calibration dependence was measured. Sulfathiazole was successfully dissolved in water at a concentration of c = 1·10-3 mol l-1 and Britton-Robinson buffer was used as the electrolyte. As the optimal pH was determined pH 6,0. At this pH, a relative standard deviation of sr = 5% was achieved. Standart deviation of 5 % has been achieved when the working electrode was polished before each measurement. Under these conditions, was calibration dependence measured in concentration range from 0,1 to 100 μmol l-1 . Linear dynamic range was calculated between 0,1 - 20 μmol l-1 . Limit of quantitation was found to be 97 nmol l-1 .
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Voltammetric detection of 7α-hydroxycholesterol on boron doped diamond electrode
Serbanová, Lucie ; Schwarzová, Karolina (advisor) ; Nesměrák, Karel (referee)
This bachelor's thesis is dedicated to the electrochemical determination of 7α-hydroxycholesterol (7α-OHC) using boron-doped diamond electrode (BDDE). The work includes the optimization of experimental conditions and the measurement of the concentration dependence of 7α-OHC. The influence of various factors, such as water content in the solution and scan rate, on the electrochemical response of 7α-OHC was investigated. Various electrochemical methods, including cyclic voltammetry and differential pulse voltammetry, were used in the experiments. The electrochemical behavior of 7α-OHC in a solution of chloric acid and acetonitrile were analyzed. Important factors such as electrode passivation and response stability were carefully evaluated. The measurement of concentration dependence of 7α-OHC exhibited a linear response within the concentration range from 2∙10−5 mol l−1 to 1∙10−4 mol l−1 . Limits of detection (LOD) and quantification (LOQ) of 1,33 µmol l−1 and 4,43 µmol l−1 were determined. Comparison with other methods revealed that the electrochemical determination of 7α-OHC on BDDE achieves comparable sensitivity. The results of this work provide crucial insights into the electrochemical behavior of 7α-OHC, highlighting the advantages of BDDE for sensitive and reliable determination of...
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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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Development of voltammetric methods for detection of phytosterols on carbon-based electrodes
Zelenský, Michal ; Schwarzová, Karolina (advisor) ; Fischer, Jan (referee)
The aim of this diploma thesis was to develop an electrochemical method for three phytosterols, namely stigmasterol β-sitosterol and ergosterol using voltammetry techniques on glassy carbon electrode and boron doped diamond electrode. The work builds on previous results, where it was shown that the electrochemical oxidation of phytosterols requires perchloric acid in acetonitrile. When this acid is used, a dehydration reaction occurs. Calibration dependences were measured here for all phytosterols in an environment with a water content of 0.43%. The stability of the signal with increasing distilled water content was further investigated. Then the calibration dependences in the increased water content were measured again. If we want to use HPLC-type separation techniques, we must first find out how the phytosterols will behave in this environment, and therefore the signal stability on the buffer content was investigated. The buffers used were phosphate and acetate buffer. Subsequently, the concentration dependence was measured in an environment with a higher content of phosphate buffer. Furthermore, the possibility of detecting two phytosterols at once was investigated. Key words: dehydration, glassy carbon electrode, boron doped diamond electrode, oxidation, phytosterols, voltammetry
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Development of electroanalytical methods for detection of bile acids possessing 7α hydroxyl group
Jelšíková, Kristýna ; Schwarzová, Karolina (advisor) ; Dejmková, Hana (referee)
This master's thesis contains a study of electrochemical processes of selected bile acids possessing 7 hydroxyl group (cholic, chenodeoxycholic and −muricholic). The measurements were performed on boron−doped diamond electrode in the non-aqueous medium of acetonitrile and perchloric acid (water content 0.55 %) by cyclic voltammetry. It is known that the electrochemical activity of 7 bile acids is increased by a dehydration reaction between perchloric acid and the 7 bile acid. The subject of the study was the stability of the voltammetric response of chemically activated bile acids in the region of negative potentials. It was found that the presence of oxygen in the measured solution is an important factor for obtaining the cathodic signal of 7 bile acids. It probably performs a regenerative function; the product of the electrochemical reduction is re-oxidized in its presence, which leads to an increase in the voltammetric response. At the same time, it is important that the direction of the scan in cyclic voltammetry first proceeds to positive values. A potential of +2.0 V (vs. Ag/AgNO3 in acetonitrile) must be reached for the HO● radicals to be formed. It is these radicals that presumably lead to the formation of the product(s) of bile acids electrochemical oxidation that can be subsequently...
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Optimization of anodic and cathodic pre-treatments of boron doped diamond electrode surfaces for electroanalysis
Baudisová, Kateřina ; Fischer, Jan (advisor) ; Dejmková, Hana (referee)
This bachelor thesis deals with the optimization of anodic and cathodic pretreatment of BDD electrodes and subsequent comprehensive characterization and comparison of electrochemical parameters of unmodified, O-terminated and H-terminated BDD electrodes. The study was carried out using cyclic voltammetry of two model inner sphere redox systems [Fe(CN)6]4−/3− and dopamine/dopamine-o-quinone. Boron concentrations in the BDD films ranged from 500 ppm to 8000 ppm. O-termination of the electrode surface was most effectively achieved when an activation potential of Eakt = +3.0 V was inserted for 10 min into 0.5 mol l−1 H2SO4. For the dopamine/dopamine-o-quinone system, the O-terminated BDD electrodes caused deceleration of electron transfer compared to the unmodified BDD electrodes, which was accompanied by an increase in the potential difference with the highest ΔEp at 500 ppm BBD electrode (ΔEp = 711 mV). To achieve the H-terminal surface, single and cumulative reduction was tested by inserting Eakt = −3.0 V. A sufficient single reduction time for the [Fe(CN)6]4−/3− system was determined to be 60 s, whereas in the case of dopamine, the electrochemical parameters did not stabilize at the selected reduction times, but the cathodic and anodic peak signal at the H-terminated 1000 ppm BDD electrode was up...
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Determination of cholesterol, 7-dehydrocholesterol and cholecalciferol by HPLC with spectrophotometric and electrochemical detection
Dostálková, Lucie ; Schwarzová, Karolina (advisor) ; Vyskočil, Vlastimil (referee)
The aim of this thesis is to verify the possibility of simultaneous determination of three structurally related biologically active substances (cholesterol, 7-dehydrocholesterol and cholecalciferol) after previous separation by high-performance liquid chromatography followed by electrochemical (on a boron-doped diamond electrode) and spectrophotometric detection, which were compared in this work. The influence of the water content in the mobile phase (in the range of 0-10 %) on the retention factor of the analytes and their response for both types of detectors was investigated. Using all mentioted water contents, the analytes baseline-separated. As the water content increased, the retention factor of the analytes increased as well as the background current for higher positive detection potentials. Based on the recorded hydrodynamic voltammograms, the optimum detection potential + 1.8 V was chosen. The optimum wavelength for spectrophotometric detection was 200 nm. The concentration dependence was measured in an of 50 mmol l−1 sodium perchlorate in acetonitrile mixed with water (95:5, v/v). The spectrophotometric detector provided lower detection limits compared with the electrochemical detector, which had detection limits of 2.3 μmol l−1 for cholesterol, 1.4 μmol l−1 for 7-dehydrocholesterol and...
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Development of voltammetric methods for detection of bile acids and their conjugates
Petráňová, Karolína ; Schwarzová, Karolina (advisor) ; Nesměrák, Karel (referee)
The aim of this thesis is to study the electrochemical properties of bile acids and their conjugates. Specifically, cholic acid, chenodeoxycholic acid, taurocholic acid, taurochenodeoxycholic acid, glycocholic acid, and glycochenodeoxycholic acid were studied. The measurements were carried out on a boron-doped diamond electrode in an environment of acetonitrile and perchloric acid, with a water content of 0.55% in the solution by method of cyclic voltammetry. In order for bile acids to be electrochemically active, they must first be dehydrated, which takes place in a reaction with perchloric acid. This reaction requires a relatively long time, so it was accelerated by heating the compounds. The goal of this work was to determine the conditions under which the dehydration products of bile acids can be detected. The water content that can be added to the solution after dehydration to keep the voltammetric signal stable was determined. Furthermore, it was found that the voltammetric determination can be carried out even at a pH that is not extremely acidic in which is the the dehydration carried out. Finally, calibration dependencies were compiled.
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Study of degradation behavior of abacavir using a diamond film electrode
Pražáková, Lucie ; Kubíčková, Anna (advisor) ; Kozlík, Petr (referee)
In this work the electrochemical degradation behavior of the drug abacavir is studied with the use of boron-doped diamond electrode. Oxidative degradation of the active substance abacavir, used to treat patients with HIV disease, was studied in a batch of three-electrode and two-electrode settings. In this work, the characteristics of five working boron-doped diamond electrodes, differing in a boron/carbon doping ratio of 500 ppm, 1000 ppm, 2000 ppm, 4000 ppm and 8000 ppm, were studied. The degradation in the three-electrode arrangement took place under potenciostatic electrolysis at potentials from 0,6 V to 2,0 V. The degradation in the two-electrode arrangement took place under conditions of potenciostatic electrolysis at higher potentials from 2,0 to 4,5 V. Optimal degradation, to the required values up to 25 %, was achieved at a potential of 3,5 V for an oxidation time of 10 minutes on a boron-doped diamond electrode with a boron/carbon doping ratio of 500 ppm and 1000 ppm. Separation and determination of abacavir and its degradation products were performed by ultra-high performance liquid chromatography with a mass detector. The degradation of abacavir produced two known degradation products, DP1 with relative retention times of 0,40 and DP2 with relative retention times of 0,45. The...
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Voltammetric detection of stigmasterol at boron-doped diamond electrode in mixed media
Benešová, Lenka ; Schwarzová, Karolina (advisor) ; Nesměrák, Karel (referee)
V o l t a m m e t r i c d e t e c t i o n o f s t i g m a s t e r o l a t b o r o n d o p e d d i a m o n d e l e c t r o d e i n m i x e d m e d i a L e n k a B e n e š o v á Univerzita Karlova v Praze Přírodovědecká fakulta Praha 2015 Abstract The aims of the study thesis was to suggest suitable solvent for oxidation of stigmasterol on boron doped diamond electrode. Cyclic voltammetry in mixed media of water and organic solvents was used for this purpose. First of all, the effect of organic solvent on potential window of boron doped diamond electrode was studied. Solvents used were methanole, isopropanole, N-dimethylformamide and acetonitrile; the water components was phosphate buffer (0,075 mol.l-1, pH 3,0). It was deduced from the results, that suitable solvent for detection of stigmasterol on was the acetonitrile, which provided sufficiently large potential window in anodic area. Keywords: boron doped diamond electrode, cyclic voltammetry, organic solvent, oxidation, stigmasterol
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