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Complexes of 2,6-bis[(N-methylpiperazine-1-yl)methyl]-4-formyl phenol
Marečková, Vendula ; Vojtíšek, Pavel (advisor) ; Kubíček, Vojtěch (referee)
Thirteen new dinuclear complexes of ligand 2,6-bis[(N-methylpiperazine-1- yl)methyl]-4-formyl phenol (L1) were prepared. Copper(II) and palladium(II) salts were used for the syntheses. Following compounds were prepared: [Cu2L1(CH3COO)2]ClO4, [Cu2L1(CF3COO)2(ClO4)][Cu2L1(CF3COO)2]ClO4, [Pd2L1(CH3COO)3], [Pd2L1(CF3COO)3], [Pd2L1(Cl)4]. These ones should act as anion receptors. The acetates were exchanged for phenylphosphinates in the case of the complex cation [Cu2L1(CH3COO)2]+ and the structure of [Cu2L1(phPO2H)2]ClO4 was obtained. Geometry of coordination shell of Cu2+ - ions in prepared complexes is tetragonal pyramid. The UV-VIS spectroscopy was used for study of interactions in system of the ligand - metal - anion. Interactions between the ligand and metals in oxidation state 2 were observed as well as interactions between the complex [Cu2L1(CH3COO)2]ClO4 and sodium salts.
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The tetrathiofulvalene derivatives: Their synthesis and properties
Nejedlý, Jindřich ; Starý, Ivo (advisor) ; Hocek, Michal (referee)
The goal of the diploma thesis was to prepare a spectrum of electron-rich macrocyclic derivatives of tetrathiafulvalene (TTF), which should serve as electron donors in interactions with electron-deficient acceptor molecules. A two-step synthesis was used for their preparation. First, a non-cyclic three-segment precursor was prepared by a reaction of a thiolate TTF construction block with a bis(bromomethyl)aromate. Then, a reaction of this precursor with another molecule of bis(bromomethyl)derivative closed the macrocycle. The latter reaction produced mainly [2+2] macrocycles containing two TTF and two aromatic units. In most cases, larger [4+4] macrocycles were also isolated from the reaction mixture. Besides thiolate TTF unit two other thiolate units, one with extended TTF core and other with smaller trithiafulvene ring, were used analogically in synthesis. By a combination of three thiolate blocks and five bis(bromomethyl)aromates 11 three-segment components were prepared and these were converted to 11 structural types of macrocycles with [2+2] and 7 macrocycles with [4+4] stoichiometry. The resulting macrocycles were characterized by 1 H a 13 C NMR spectroscopy and analyzed by a gel permeation chromatography. Their structures were also confirmed by high-resolution mass spectroscopy. Interaction...
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Optimizing the determination of distribution of surfactant at phase separation in polymer-surfactant system
Sátorová, Kateřina ; Pekař, Miloslav (referee) ; Mravec, Filip (advisor)
This diploma thesis is focused on the determination of distribution a surfactant at phase separation in polymer-surfactant system. Sodium hyaluronate of three molecular weights was chosen as a polymer, CTAB was used as a surfactant. The experiments were performed in an environment of 0,15 M NaCl. The measurement of the CTAB concentration in samples was based on the formation of coloured complexes of CTAB and picric acid in chloroform. UV-VIS spectroscopy was used for the detection of these complexes. The content of CTAB was determined in four gels of different composition (2% Hya + 200 mM CTAB, 2 % Hya + 50 mM CTAB, 0,5 % Hya + 200 mM CTAB, 0,5 % Hya + 50 mM CTAB). All gels were gradually washed five times with 0,15 M NaCl. The content of CTAB was determined for newly prepared gels and for gels after 2 and 4 months since the preparation. Initial concentrations of CTAB and hyaluronan have greater influence on the distribution of CTAB after phase separation, than the molecular weight of hyaluronan. The content of CTAB in newly prepared gels and after 4 months since preparation is very similar and demonstrates the stability of the system.
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Dialysis study of hyaluronan-surfactant interactions
Šejnohová, Michaela ; Venerová, Tereza (referee) ; Pekař, Miloslav (advisor)
This diploma thesis is concentrated on the interactions between polyelectrolyte (hyaluronan) and cationic surfactant (CTAB). The experiments were performed in an aqueous solution and in an environment of physiological ionic strength (0,15mmoldm-3 NaCl). The determination of the surfactant concentration in solutions was based on the formation of colored complexes of CTAB and picric acid in chloroform. The concentrations of surfactant were measured by UV-VIS spectroscopy. The stability of CTAB+HyA was examined by a dialysis method. The results showed that, regardless of the environment, the presence of HyA in solution reduces the number of free molecules of CTAB which can be determined in the sample. It has been proved that there is an interaction between HyA and surfactant and that CTAB has greater affinity for HyA then for the picric acid. The stability of CTAB+HyA was determined by dialysis of 120 hours. After that time, the concentrations of the retentate and permeate were settled. The results showed that in the membrane remains a certain amount of CTAB bounded to hyaluronan. The system can be suitable for the preparation of targeted carriers of biologically active substances.
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Diaphragm discharge in organic dye solutions
Pajurková, Jana ; Možíšková, Petra (referee) ; Kozáková, Zdenka (advisor)
This Diploma thesis was focused on the degradation of dyes Saturn Red L4B (Direct Red 79) and Saturn Blue LB (Direct Blue 106) by DC diaphragm discharge (DC-DD). Supplied power was between 160 and 180 W. Conductivity and pH were changing at each electrode area during the DC diaphragm discharge, therefore the effect of pH and conductivity changes on the dye solution itself were examined. All samples were measured by UV-VIS spectrometer in the wavelength range of 300–800 nm. No significant dependence of dye absorption spectra on conductivity was observed, while pH significantly affected the absorption curves of dyes. Ageing of dye spectra showed significant changes of Saturn Red L4B. Next task was the comparison of dyes destruction efficiency by DC-DD, audiofrequency diaphragm discharge (AF-DD) and electrolysis. Dye decomposition by AF-DD was not observed at set conditions (voltage of 80–120 V, current of 2.2 A and frequency of 2 kHz). In the case of DC diaphragm discharge the electrolysis played an important role. Decomposition efficiency of the dyes by electrolysis was up to 15 %. The pumping effect in the DC diaphragm discharge was also investigated. Although the individual electrode areas were linked only by a small pinhole in a nonconductive barrier (the pinhole diameter of 0.3 mm), solutions of the anode and cathode compartment interacted with each other up to 10 %. Finally, the degradation products of Saturn Red L4B treated by DC-DD in two electrodes parts are also described. Decomposition products were determined by high performance liquid chromatography (HPLC) combined with the mass spectrometer.
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Diaphragm discharge in organic dye solutions with focus on electrolytic decomposition
Davidová, Jaroslava ; Brablec, Antonín (referee) ; Kozáková, Zdenka (advisor)
This Diploma thesis is focused on physical and chemical effects which contribute to the decomposition of organic dyes by diaphragm discharge generated in water solutions. Due to the application of DC high voltage source in continuous regime, there is an effect of electrolysis contributing to the dye decomposition by diaphragm discharge. The aim of this work was to find out when the electrolysis is running (or when is the moment of discharge breakdown) and which factors influence the breakdown. The other goal was decomposition of selected textile and food organic dyes by electrolysis itself. In the theoretical part, theory about creation of electrical discharges in aqueous solutions is noted and various types of underwater discharges are described. Background researches about underwater electrical discharges used in the world are mentioned as well as the use of diaphragm discharges and various ways how to remove organic dyes from wastewater. Finally, theories of electrolysis, UV-VIS spectroscopy and basis of other analytical methods useful for detection of organic molecules are described. Experimental part is oriented to experiment procedure which was carried out in a reactor with separated electrode areas. Separation was made by dielectric diaphragm with a pinhole in the centre. Its initial diameter was 0.4 mm. Used chemicals and course of experiments are described in this part, too. First, the breakdown moment in the reactor was investigated (i. e. determination, when only electrolysis was operating) by formation of hydrogen peroxide and measurement of dynamic (time resolved) electrical characteristics. Next, decomposition of selected dyes by electrolysis was carried out. As the decomposition was related to decolorization of the solution, UV-VIS spectroscopy in the range of 350–700 nm was used for determination of dye concentration. Next part focused on results presents various factors which had an effect on breakdown of diaphragm discharge. These factors are kind of used electrolyte, initial conductivity of solution, kind of dye, temperature of solution and type of reactor (or solution volume). From the result, the most important factor is initial solution conductivity. After the determination of the breakdown moment, the electrolysis of organic dyes was performed. The applied current was 10 mA, initial conductivity was 500 µS/cm and used electrolyte was NaCl. Moreover comparison of dye decomposition in dependence on the different applied power was realized. From this comparison one can assume, there is no significant contribution of electrolysis (the efficiency is approximately 15 %) to the diaphragm discharge in aqueous solution.
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Study of influence of organic dye structure on their decomposition in the diaphragm discharge in liquids
Pajurková, Jana ; Fasurová, Naděžda (referee) ; Kozáková, Zdenka (advisor)
The main goal of presented thesis is to study the influence of organic dyes structure on its degradation in diaphragm discharge in liquids. Diaphragm discharge is a kind of non-thermal plasma that can be generated in liquids by the application of high voltage. In plasma channels (so-called streamers), many physical and chemical processes are formed. High electrical field, shock waves and last but not least emission of electromagnetic waves in the range of visible and ultra-violet radiation appear among physical processes. The most important chemical process is generation of active species. These species initiate chemical reactions and could attack molecules of organic compounds contained in water solution. The reason why organic dyes were chosen in this study is its visible destruction, because it is related to its decolouration. Further, UV-VIS spectroscopy for the determination of concentration during the experiment can be used. Organic dyes are good models of organic substance often contained in waste water and for which removal classical biological, chemical and physical methods aren’t sufficient. Selected dyes were mostly from the group of azo-dyes: Acid Red 14, Acid Red 18, Acid Yellow 23, Direct Blue 53, Direct Red 79, Direct Red 80, Direct Yellow 29, Food Yellow 3 and further, Acid Blue 74 (indigotic dye) and Direct Blue 106 (oxazine dye). Experiments were carried out in a special batch discharge reactor with the anode and the cathode spaces divided by a non-conductive barrier, where the diaphragm with a pin-hole was placed. Measurement showed different removal in the anode and cathode space. We have supposed it was caused by different streamers features and energetic conditions. Dyes were decomposed with higher efficiency in the anode space where the final concentration reached 40 % of the initial concentration while it remained about 90 % in the cathode space. In this thesis the influence of dyes structure on the dye decomposition by electrical discharge was investigated. Dyes consisted of small molecules and dyes with many substitutes bounded on aromatic ring were decomposed more easily than dyes consisted of big molecules. The shift of characteristic wavelength on both directions (to shorter as well as longer wavelength) was observed during the experiments especially when the Direct dyes were decomposed. This phenomenon was probably due to the formation of intermediate product, which have different characteristic wavelength than the primary compound. In general, colourfulness is given by long conjugated systems of double bonds with substitutes bounded on an aromatic ring. Each change in the molecule structure provides the colour change and this could be the possible reason of the shift of characteristic wavelength. The other task was the comparison of degradation process efficiency by the mean of electrolysis and diaphragm discharge. Results showed that electrolysis (30 W) was more convenient for degradation of dyes consisted of small molecules while diaphragm discharge (130170 W) suited for complex molecules. For degradation of small molecules, oxidation on the anode assumed to be the most effective process that is initiated by electrolysis. For degradation of big molecules, attack of active species produced by the discharge is necessary.
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Study of electrolytic influence on organic dye decomposition in the diaphragm discharge in liquids
Davidová, Jaroslava ; Rašková, Zuzana (referee) ; Kozáková, Zdenka (advisor)
This Bachelor thesis is focused on study of chemical and physical influences which are proceed in diaphragm discharge in water solution. These processes could be used in water treatment. If DC non-pulsed voltage is applied, a significant influence of electrolysis must be taken into account. The main goal of this thesis is the estimation of electrolytic contribution to processes in the discharge. Theoretical part describes basic theory about creation of electrical discharges in water and electrolysis with emphasis on processes leading to destruction of organic compounds. Production of reactive particles (radicals, hydrogen peroxide, ozone, etc.) and electrochemical reactions on electrodes mainly belongs among these processes. This part describes analytical method (UV-VIS spectroscopy) which was used for determination of organic dyes concentration as well. Experimental part is oriented to experiment procedure which was carried out in an apparatus with separated anode and cathode area. Separation was made by dielectric diaphragm with a pinhole in the centre. Its initial diameter was 0.25 mm. Electrolytic decomposition was carried out at constant current of 30 mA and supplied power was about 14–32 W. Two Saturn dyes (Direct Blue 106 and Direct Red 79) were selected for experiments. As the decomposition was related to decoloration of the solution, UV-VIS spectroscopy in the range of 350–700 nm was used for determination of dye concentration. Next part focused on results presents various factors which had remarkable effect on decomposition of organic dyes. These factors were: various polarities of electrodes, conductivity and pH of solution, applied power, kind of electrolyte and structure of organic dye. The electrolysis had the significant influence on decomposition of small organic molecules. Decomposition was running mainly in the anode area where so called negative discharge was created. Optimal conditions were set by NaCl electrolyte with concentration providing initial conductivity of 500 S·cm-1. By the NaNO3 electrolyte half decomposition efficiency was achieved and in Na3PO4 electrolyte, the decomposition even didn’t run. The decomposition in the anode area was stimulated by the low pH value, which was decreasing during electrolysis. Generally, higher decomposition was achieved by the discharge than by pure electrolysis but the electrolysis had higher efficiency. In pure electrolysis, high rate of removal can be achieved by the application of a relatively low power. When bigger organic molecules were decomposed, the efficiency was higher by applying the discharge.
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Absorbance humusových látek černozemí v ultrafialové a viditelné oblasti spektra
Brychtová, Martina
Abstract In bachelor thesis we aimed at evaluation of humic substances quality using visible and ultraviolet spectroscopy. Object of our study were ten subtypes of Chernozems. UV-VIS spectra were recorded within the range 200 nm to 700 nm. Absorbance indexes were calculated at: 253/203, 253/230, 250/365, 253/410, 465/665 a 255/465 nm. Results showed differences in absorbance indexes values between chernozem subtypes. Lower absorbance was characteristic Arenic Chernozemkých and higher for Phaeoic Chernozem. One of most important was the absorbance index at 465/665 nm.
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