|
|
Removal of selected organic pollutants from water using advanced oxidation processes
Dalajková, Nikola ; Vávrová, Milada (referee) ; Repková, Martina (advisor)
The aim of this diploma thesis is the determination of selected organic pollutants with a focus on artificial sweeteners in waste water from wastewater treatment plant (WWTP) Modřice and the subsequent degradation of the thus obtained concentrations in model water using advanced oxidation processes (AOP). Two sweeteners were determined, namely sucralose and saccharin found in waste water. Synthetic sweeteners are not sufficiently cleaned in the WWTP and penetrate the environment. Effective processes for removing organic substances, including alternative sweeteners, are AOP processes. These processes are based on reactions of highly reactive hydroxyl radical (OH·), which is produced by many chemical reactions. Generally, they use ozone (O3) and hydrogen peroxide (H2O2). On sampling, wastewater samples were treated with Solid Phase Extraction (SPE) and then evaluated by HPLC/MS (High Performance Liquid Chromatography). In observing the degradation of selected sweeteners, three AOP methods were used: O3/UV, H2O2/UV and O3/H2O2. For each of these methods, the efficiency of degradation of sucralose and saccharin was investigated. From the evaluated data it was found that the most efficient AOP process for removing artificial sweeteners from water is the O3/H2O2 method.
|
|
|
Study of changes in the chemical composition of coffee during roasting
Kohoutová, Lenka ; Vítová, Eva (referee) ; Diviš, Pavel (advisor)
This bachelor thesis deals with monitoring of changes in acrylamide and hydroxymethylfurfural levels in coffee during the process of roasting. Green coffee was roasted using two separate roasting modes (medium roast: temperature 210 °C for duration of 14 minutes, City roast: temperature 220 °C for 17 minutes). Concentration of acrylamide and hydroxymethylfurfural for various roasting durations was determined by high performance liquid chromatography. For the determination of acrylamide, linear growth of the concentration was observed. The final levels of acrylamide corresponded with levels given by the literature, although the characteristic trend of acrylamide formation was not observed. Typical trend of hydroxymethylfurfural formation was observed in samples roasted with City roast mode, while the first part of the trend was also apparent in samples roasted with medium roast mode. Final levels of hydroxymethylfurfural in roasted coffee were within the limits given by the literature.
|
|
|
Optimalization of the extraction of bioactive compounds from herbs into different kind of oil bases
Chytil, Dalibor ; Zemanová, Jana (referee) ; Pořízka, Jaromír (advisor)
This diploma thesis deals with the optimization of processes for extraction of bioactive lipophilic compounds from fruits of sea buckthorn (Hippophae Rhamnoides) into various types of plant oil bases using simple maceration. The theoretical part of this thesis deals with the characterization of this herb, its botanical classification, traditional use, chemical composition and medicinal effects. Increased attention is also paid to the characterization of individual types of plant oils used, namely camellia, camellia organic, passionflower, kukui and kiwi oil. The experimental part of the thesis deals with application of theoretical knowledge. The profile of total and free fatty acids for individual plant oil bases was determined by GC/FID, furthet the basic fat numbers were also determined. When optimizing the extraction, emphasis was placed not only on the effect of the extraction agent used, but also on the extraction time (1, 3, 5, 7, 10, 14, 21 and 66 days). The macerates were continuously subjected to the determination of selected parameters (total amount of carotenoids, total amount of phytosterols, lutein, neoxanthin, astaxanthin, stigmasterol, -sitosterol and vitamin E) using UV-VIS spectroscopy and HPLC/PDA. Likewise, the peroxide number was monitored during maceration to assess the degree of oxidative degradation of macerates. The recovery of selected total parameters in individual oils did not differ significantly in most cases. On the contrary, the yield of individual monitored parameters differed significantly. At the same time, static maceration under our conditions was not very suitable for the extraction of vitamin E, stigmasterol and total phytosterols.
|
|
|
Determination of antibiotics in the soil ecosystem
Brož, Tomáš ; Zlámalová Gargošová, Helena (referee) ; Mravcová, Ludmila (advisor)
This work deals with a current issue of increasing drug concentrations and thus the growing number of resistant bacteria in the soil. One of the problem helping this issue is the fertilization of agricultural fields with animal faeces, in which antibiotics occur in an unchanged and still active form, as well as the insufficient effectiveness of conventional methods used in wastewater treatment plants. In an effort to improve the monitoring of this problem, a method for the determination of these antibacterial agents in the soil matrix, using solid phase extraction, and also a UPLC/MS method for their evaluation have been developed and optimized. From the group of sulfonamide antibiotics, sulfacetamide, sulfadiazole, sulfamerazine, sulfamethazine, sulfamethoxazole, sulfapyridine, sulfasalazine, sulfathiaosal and trimethoprim were selected. The lowest limit of detection for the method is 0.3 µg/g for sulfathiazole and the highest of 8.1 µg/g for sulfasalazine. The highest average yields were achieved with sulfamethoxazole, namely 63 ±8 %.
|
|
|
Determination of macrolides in wastewater during the technology applied to wastewater treatment plants
Landová, Pavlína ; Čáslavský, Josef (referee) ; Vávrová, Milada (advisor)
Diploma thesis is focused on determination of macrolide antibiotics in wastewater. Environmental contamination with drugs currently represents a major problem. To determine the level of contamination is necessary to develop the appropriate analytical techniques. From the group of macrolide antibiotics were selected four representatives: erythromycin, clarithromycin, azithromycin and roxithromycin due to their frequent use in Czech Republic. For their isolation from wastewater was selected solid phase extraction and for analysis high performance liquid chromatography with mass spectrometric detection was chosen. Under optimized conditions, the ten days analysis of wastewater from the WWTP Brno-Modřice, two days analysis of wastewater from the WWTP Mikulov and one day analysis of wastewater from WWTP of University of Veterinary and Pharmaceutical Sciences Brno was performed.
|
|
|
Study of sorption properties of biochar
Kocinger, Oskar ; Řezáčová, Veronika (referee) ; Mravcová, Ludmila (advisor)
This diploma thesis deals with sorption properties of biochar produced from wood biomass treated with concentrated hydrochloric acid and activated carbon with respect to the triazine pesticide propazine. Although pesticides are widely used in both agriculture and the private sector worldwide, they pose a significant risk to ecosystems and human health. Propazine belongs to the group of chlorinated triazine herbicides, which pose a risk mainly as endocrine disruptors. The sorption of organic pollutants using pyrogenic carbonaceous materials promises an efficient and economically affordable solution, which has recently received increasing attention from the scientific community. In this work, we used isotherms to describe the equilibria of propazine sorption to given sorbents during vial experiments. Analysis of the propazine content in the model water solutions after reaching equilibrium was performed using high-performance liquid chromatography with mass detection.
|
|
| |
|
|
PCP sorption of lignite
Šnédarová, Gabriela ; Taraba, Boleslav (referee) ; Pekař, Miloslav (advisor)
Within the framework of this diploma thesis, the sorptive capability of a lignite as a natural adsorbent was applied on an aqueous solution of pentachlorophenol. The aqueous solution of this substance, which is very dangerous for the environment, was prepared in various concentration ranges according to reached solubility. The solubility is noticed in different literatures variously and then is not applicable. That is why it was necessary to find out the ”real“ solubility. The aqueous solution of pentachlorophenol of given concentration was subsequently put to adsorption with exactly defined quantity of the lignite and as a result the adsorptive isotherms were obtained. These isotherms represent the adsorption capability in dependence on the adsorption duration, quantity of used lignite and concentration of pentachlorophenol solution. By the adsorption with duration longer than one hour, the quantity of adsorbed PCP does not increase markedly.
|
|
|
Multidimensional Liquid Phase Separations
Šesták, Jozef ; Čáslavský, Josef (referee) ; Pulkrabová, Jana (referee) ; Česla, Petr (referee) ; Kahle, Vladislav (advisor)
This dissertation is dedicated to the topic of multidimensional liquid phase separations. This separation techniques are developed for analysis of complex samples containing thermally labile, low volatile or high molecular weight components that can´t be analysed by two-dimensional (2D) gas chromatography. Concepts of peak capacity and orthogonality are explained and various methods of their determination are stated in theoretical part of dissertation. High performance column liquid chromatography (HPLC) and high performance capillary electrophoresis (HPCE) are suggested as the most suitable methods for automated multidimensional liquid phase separations on-line coupled to mass spectrometry. Configuration of simplified miniaturized liquid chromatograph is described in experimental part of this thesis. Original concept of the system has been extended by simple mobile phase gradient generation technique. Correct function was demonstrated on repeatable separation of alkylphenones, peptides, nitroaromatics, and nitroesters. This system has been utilized as a base for a couple of simple two-dimensional separation platforms for HILIC-MALDI-MS analysis of glycans, for separation of peptides based on off-line coupling of isoelectric focusing and capillary liquid chromatography, and finally for on-line IEC×RPLC, RPLC×RPLC, and HILIC×RPLC two-dimensional liquid chromatography. Correct operation of submitted platforms has been proved.
|
|
|
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...
|
guest ::
