National Repository of Grey Literature 153 records found  beginprevious93 - 102nextend  jump to record: Search took 0.01 seconds. 
Reactivity and controll of properties of metallic materials
Tkacz, Jakub ; Šoukal, František (referee) ; Zmrzlý, Martin (advisor)
This thesis is focused on corrosion protection of magnesium alloys AZ 91. Very important is material corrosion in some environments and last but not least surface treatment as grinding, polishing and etching. Theoretical part of this thesis is about magnesium and magnesium alloy. It focuses on properties, in order to determine the best procedure for corrosion protection. It characterize material corrosion- for example corrosion in special environment (atmosphere, water, etc.) or elektrolyte corrosion. Big part of theoretical part is focused on electrochemistry, in particular kinetic aspects (Tafel diagrams, corrosion current, etc.) and potentiostatic testing, where are observed properties of material in relation to potential: corrosion potential Ecorr, brakedown potential Ebd and repassivation potential Erp. This work present preparing, utilization and positive or negative aspects of corrosion protection. Metallography is important too since metallographical preparation is crucial for the research on the material. Described metallography procedures are mounting, grinding, polishing, etching and interpretation. Experimental part of this thesis is in particular about corrosion properties of magnesium alloy AZ 91. It focuses on calculation of corrosion rate in defferent environments. Principle is mass defekt of the alloy. The environments are: destilled water, hot service water and 3% NaCl solution (like sea water). Last but not least are important. procedure manipulation with materials. Very important are choice and composition of solutions, etching time, choice of polishing cloth, lubricant solution and good pressure. Beacuse of this aspects can be show corrosion action of environments on magnesium alloy AZ 91 by photographies.
Fabrication of Nanowires into Porous Alumina by Electrolysis
Staňo, Michal ; Čechal, Jan (referee) ; Škoda, David (advisor)
This thesis deals with preparation of metal nanowires based on electrodeposition from aqua solution of metallic salts into porous dielectric aluminium oxide templates. The theoretical part covers various bottom-up methods of nanowire preparation using a template, electrochemistry and electrodeposition overview. The Experimental part is focused on the nanowire (Ag, Cu, Ni-H) preparation by means of direct current and alternating current electrodepositon and geometrical characterization of fabricated nanowires by scanning electron and atomic force microscopy. Defects of commercially available and prepared porous alumina templates are mentioned. Branching and coalescence of nanowires are briefly discussed as well.
Unique Properties of Amalgam Electrodes
Josypčuk, Bohdan ; Josypčuk, Oksana
Depending on metal-mercury ratio and on the method of preparation amalgam can be: 1) solid compact; 2) paste; 3) liquid; 4) monocrystalline; 5) porous; 6) powdered. High potential of hydrogen overvoltage is observed on amalgam electrodes and it is comparable with one on Hg-electrodes. Another important benefit is the possibility to prepare amalgam electrode, detector or reactor of required size and shape. From amalgams have been prepared and tested many types of electrodes for batch and flow-through systems. The diversity of amalgam materials provides some unique electrochemical properties of electrodes, the most important of which are described in this paper.
Magnetic Beads-Based Electrochemical Techniques for DNA-Protein Interaction Monitoring
Fojta, Miroslav ; Pivoňková, Hana ; Němcová, Kateřina ; Horáková Brázdilová, Petra ; Havran, Luděk ; Orság, Petr ; Vidláková, Pavlína ; Macíčková-Cahová, Hana ; Balintová, Jana ; Hocek, Michal
Electrochemical techniques, in connection with separation of nucleoprotein complexes at magnetic beads, are suitable for the monitoring of DNA-protein interactions. For the detection of complexes captured at the beads it is possible to utilize intrinsic electrochemical activity of the protein, intrinsic structure-selective signals of the DNA, or indicator DNA substrates tail-labeled with electroactive moieties.
Electrochemistry of Polynitrocalix-[4]-arenes
Liška, Alan ; Ludvík, Jiří
Calix[4]arene is a suitable inert and stable frame for building "smart" molecules and supramolecular assemblies. Polynitrocalix[4]arenes where reducible nitro groups are located at the upper rim are promising precursors for aimed development of sensors. In this work a series of mono-, di-, tri- and tetra nitroderivatives was reduced, the sequence of individual steps was described and the mechanism discussed. It was found that in this molecule with several redox centers all nitro groups are electronically isolated and thus are reduced independently yielding poly-radical ions. Two different couples of equivalent nitro groups were proved in tetranitro derivatives. The experimental results were confirmed by quantum chemical calculations.
Electrochemical Reduction of 1,3-Alt-tetranitrothiacalix[4]arenes
Liška, Alan ; Ludvík, Jiří
Calixarenes are organic molecules which contain several aromatic units (in this work four) connected by methylene („calixarenes“) or sulfur („thiacalixarenes“) bridges. Calix[4]arenes can exist in four defined conformations: cone-, partial cone-, 1,2- and 1,3-alternating (Fig. 1). The conformational stability of a (thia)calix[4]arene is controlled by the size of the substituents on the upper or the lower rim, or by other interactions (e.g. hydrogen bonds). These compounds are very attractive for supramolecular chemists, since they have the shape of a cavity, being able to exhibit host-guest interaction according to the substitution 1,2. The calixarene skeleton itself is not reducible. Therefore it´s necessary to introduce a suitable redox probe in the calixarene frame in order to use electrochemical methods for investigations of calixarene properties. For the purpose of this study the nitro group was chosen because its electrochemical reduction proceeds easily in a well-defined way.
Diagnostické biosenzory pro encefalopatie způsobené priony
Šobrová, Pavlína
Prion diseases are fatal transmisible neurodegenerative and infectious disorders (TSEs) of humans and animals, characterized by structural transition of the host-encoded cellular prion protein (PrPC) into the aberrantly folded pathologic isoform PrPSc. The main aim of this work is to summarize present information about prion diseases and their possibilities of determination pointed to electrochemical techniques. For this purpose cyclic voltammetry (CV), differential pulse voltammetry, differential pulse voltammetry Brdicka reaction and chronopotentiometric stripping analysis (CPSA) were used. The estimated detection limits were 32 ug/ml by CV, 16 ug/ml by DPV, 16 ug/ml by DPV -- Brdicka reaction and 8 ug/ml by CPSA. Subsequently, the influence of heat denaturation was observed. It clearly follows from the obtained results that signals of prion decreased linearly depending on the duration of the heat treatment at 99°C for various time intervals 0, 15, 30, 45, and 60 min. Moreover, we aimed our attention on studying of prion protein interaction with CdTe quantum dots (QDs) using electrochemistry. Primarily, we characterized electrochemical properties of QDs and the detection limit at 100 fg/ml was estimated. Further, electrochemical study of prion and QD interactions was carried out to find the most suitable conditions for sensitive detection of prion proteins. Detection limit (3 S/N) was estimated as 1 fg in 5 ul. This makes labeling of proteins with QDs of great importance due to easy applicability and possibility to use in miniaturized devices, which can be used in situ. This should open new possibilities how to determine the presence of these proteins on surgical equipment and other types of materials, which could be contagious.
Mechanism of Li-storage in TiO2(B) and TiO2(anatase)
Zukalová, Markéta ; Lásková, Barbora ; Kavan, Ladislav
Due to their ability to accommodate Li+, non toxicity, low cost and cycling stability TiO2(B) and anatase represent promising condidates for Li-ion batteries [1,2]. TiO2(B) is metastable modification of titanium dioxide, adopting the nanoclinic structure [3,4].
Electrochemical Characterization of TiO2 Blocking Layers for Dye-Sensitized Solar Cells
Kavan, Ladislav
Thin compact layers of TiO2 are grown by thermal oxidation of Ti, by spray pyrolysis, by electrochemical deposition, and by atomic layer deposition. These layers are used in dye-sensitized solar cells to prevent recombination of electrons from the substrate (FTO or Ti) with the hole-conducting medium at this interface. The quality of blocking is evaluated electrochemically by methylviologen, ferro/ferricyanide, and spiro-OMeTAD as the model redox probes. Two types of pinholes in the blocking layers are classified, and their effective area is quantified. Frequency-independent Mott–Schottky plots are fitted from electrochemical impedance spectroscopy. Certain films of the thicknesses of several nanometers allow distinguishing the depletion layer formation both in the TiO2 film and in the FTO substrate underneath the titania film. The excellent blocking function of thermally oxidized Ti, electrodeposited film (60 nm), and atomic-layer-deposited films (>6 nm) is documented by the relative pinhole area of less than 1%. However, the blocking behavior of electrodeposited and atomic-layer-deposited films is strongly reduced upon calcination at 500 °C. The blocking function of spray-pyrolyzed films is less good but also less sensitive to calcination. The thermally oxidized Ti is well blocking and insensitive to calcination.
Electrochemistry as a Tool for an Enzyme Characterization
Gál, M. ; Krahulec, J. ; Jiríčková, K. ; Sokolová, Romana ; Híveš, J.
Basic biochemical properties such as Michaelis constant (KM) and turnover number (kcat) of enzyme enteropeptidase was measured by electrochemical impedance spectroscopy. Both values determined by impedance measurements are in good agreement with those obtained by traditional spectroscopic techniques. Therefore one can suppose that electrochemical methods might be successful for such measurements also in the case where usual ones (UV-Vis, fluorescence spectroscopy) are not able to determine these enzyme characteristics.

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