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Dissertations / Theses on the topic 'Rychlá diferenční pulsní voltametrie'
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1
Laníková, Petra. "Studium vlivu lipozomálních platinových cytostatik na nádorové buňky pomocí voltametrických metod." Master's thesis, Vysoké učení technické v Brně. Fakulta elektrotechniky a komunikačních technologií, 2017. http://www.nusl.cz/ntk/nusl-316850.
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Aim of this thesis is voltammetric study influence of liposomal platinum cytostatics on cancer cells. One of the goals is summarize available informations about influence of cisplatine on cancer cells, its encapsulation into liposome and affection of this cytostatic cisplatin encapsulated in liposome on cancer cell lines. In literary recherche is detail description of these issues. Than is there specification of voltammetric methods, which serve to electrochemical detection of cisplatin. Based on literary recherche was chosen the best method for detection and subsequently the method was optimalized and than was applied to measuring itself.
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Koudelková, Zuzana. "Studium vlivu kvantových teček na biologické systémy a jejich komponenty." Master's thesis, Vysoké učení technické v Brně. Fakulta elektrotechniky a komunikačních technologií, 2015. http://www.nusl.cz/ntk/nusl-221351.
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The aim of this thesis is to summarize the available evidence about quantum dots and their effects on living systems. The text describes methods for the preparation of quantum dots with respect to their characteristics (size, fluorescence wavelength) and methods of quantum dots bio-functionalization of biomolecules. In living organisms is a large number of proteins, because these are considered as one of the main components of the interaction of organisms. Therefore, the work also provides basic information about proteins. Finally, there are described various methods by which the quantum dots may be characterized mainly by differential pulse voltammetry measurement zeta potential and fluorescence measurement. The main objective of this work is to propose models of different environments in which will be degradation of quantum dots with regard to the evaluation of acquired kinetic parameters for predicting the stability of individual quantum dots.
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Bavol, Dmytro. "Využití potenciálových programů při průtokovém elektrochemickém stanovení biologicky aktivních organických látek." Doctoral thesis, 2018. http://www.nusl.cz/ntk/nusl-388061.
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9 Abstract In this Ph.D. thesis possibilities of using our proposed potential programs for a multiple-pulse amperometry and a fast scan differential pulse voltammetry in combination with flow systems are presented. The development of new sensitive amperometric and voltammetric methods for the determination of oxidisable biologically active organic compounds is another aim of this work. In the first part of the work, the flow injection system and multiple-pulse amperometric detection were employed to develop and optimize a simple, low-cost, and rapid method for the simultaneous determination of natural and synthetic antioxidants. This technique involves the application of an appropriate potential waveform consisting of a suitable sequence of pulses on a single working electrode, thus allowing distinguish the analytes in a mixture with no need of separation. Conditions for the determination of antioxidants and modelling of the potential program were tested and studied, respectively. Second part of the work describes and characterizes the application of the fast scan differential pulse voltammetry (FSDPV) in combination with the flow systems. FSDPV is the electroanalytical technique that use high scan rate to record voltammograms within several milliseconds and ensures high temporal resolution. This technique...
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Venusová, Eva. "Využití elektrochemických technik pro studium apoferritinu." Master's thesis, 2019. http://www.nusl.cz/ntk/nusl-427673.
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Theme of this diploma thesis is usage of electrochemical techniques for study of apoferritin, which is artificially synthetized protein derived from ferritin. Apoferritin has empty cavity which can be used for completion of broad amount of substances. Encapsulation of anticancer drugs can decrease their unwanted side effects such as strong toxicity and therefore increase it’s effectiveness at the tumor site. Substances chosen in this diploma thesis were standard platinum and platinum drugs cisplatin and it’s analogy oxaliplatin. Measurement was performed by electrochemical method differential pulse voltammetry by which was determined encapsulation capacity of apoferritin for chosen anticancer drugs. For determination size and zeta potential of nanoparticles was used colloid analyzator ZetaSizer Nano.
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Tvrdíková, Jana. "Voltametrické stanovení dinitronaftalenů pomocí krystalové stříbrné amalgámové elektrody." Master's thesis, 2011. http://www.nusl.cz/ntk/nusl-297233.
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Voltammetric methods for determination of 1,3-dinitronaphthalene (1,3-DNN), 1,5-dinitronaphthalene (1,5-DNN) and 1,8-dinitronaphthalene (1,8-DNN) using DC voltammetry (DCV) and differential pulse voltammetry (DPV) at novel single crystal silver amalgam electrode (CAgAE) were developed in this work. Developed methods may be used for determination of 1,3-DNN within a concentration range 2 - 10 μmol.L-1 with LoQ 2 μmol.L-1 using DCV and 1 - 100 μmol.L-1 with LoQ 1 μmol.L-1 by DPV; 1,5-DNN wihin a concentration range 2 - 10 μmol.L-1 with LoQ 2 μmol.L-1 using DCV and 1 - 10 μmol.L-1 with LoQ 1 μmol.L-1 by DPV and 1,8-DNN within a concentration range 2 - 10 μmol.L-1 with LoQ 2 μmol.L-1 using DCV and 0,3 - 1 μmol.L-1 with LoQ 0,3 μmol.L-1 by DPV. An attepmt to decrease LoQ by adsorptive stripping differential pulse voltammetry was not successful. Process of electrochemical reduction of selected dinitronaphthalenes on the working electrode was also studied by cyclic voltammetry. This work verified the use of CAgAE as alternative electrode material to mercury electrodes for determination of electrochemically reducible organic compounds in aqueous-methanolic media. Small dimensions of the CAgAE are the main advantages which predetermine its use in voltammetric microvolume batch analysis and amperometric detection in...
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Murcková, Klára. "Voltametrické stanovení herbicidu Aclonifenu pomocí rtuťových elektrod." Master's thesis, 2012. http://www.nusl.cz/ntk/nusl-307470.
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Presented Diploma Thesis is focused on electroanalytical determination of the herbicide Aclonifen, which belongs to a group of herbicides derived from diphenylether. These herbicides are used due to their effects - inhibition of protoporfyrinogen oxidase synthesis and also inhibition of biosynthesis of carotenoids. Due to its widespread use in agricultural, toxical effects on humans and because of its negative impacts particularly on aquatic ecosystems there is a need for methods capable of determining the presence of Aclonifen in the environment to monitor its ecological impacts. Optimal conditions for the determination of Aclonifen have been investigated in BR buffer - methanolic solution and in BR buffer. Electrochemical behavior of the substance has been studied using direct current voltammetry (DCV), differential pulse voltammetry (DPP) and adsorptive stripping voltammetry (AdSV) on the hanging mercury drop electrode (HMDE) and by using TAST polarography and differential pulse polarography (DPP) on the dropping mercury electrode (DME). UV/VIS spectrophotometric detection was used for comparison to electrochemical detection. Used wavelengths were 308 nm and 388 nm. For electrochemical determination of Aclonifen the above mentioned techniques were used and following results were obtained: DCV...
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Bergerová, Michaela. "Stanovení indikanu na uhlíkové pastové elektrodě a uhlíkové kompozitní elektrodě." Master's thesis, 2017. http://www.nusl.cz/ntk/nusl-356149.
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This thesis is focused on the application of two working electrodes of graphite suitable for determination of oxidizable tumour biomarkers. It deals with the study of electrochemical behavior of urinary indican. For the determination the technique of differential pulse voltammetry (DPV) was used on carbon paste electrode and film composite paste electrode in Britton-Robinson (BR) buffer. In the first step optimal conditions were determined to find the lowest limit of determination (LQ) of this substance. BR buffer of pH 3 was chosen as the optimum medium for determination on a carbon paste electrode and BR buffer of pH 2 was used as the optimum medium for the determinaton using a film composite electrode. Performance for both electrodes was observed in a concentration range of from 1 · 10-6 to 5 · 10-5 mol·l-1 . The limit of determination for measurements on a carbon paste electrode was 0.7 µmol·l-1 and the film composite electrode was 1.7 µmol·l-1 . Possibility of the acummulation of indican was examined in order to increase sensitivity and decrease of limit of quantification. However, after 5 minute sorption, no increase in response was observed and the accumulation step was not inserted. Developed method was tested on the determination of urinary indican in human urine matrix after solid phase...
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Bystrianský, Martin. "Voltametrické stanovení anilazinu na stříbrné tuhé amalgámové elektrodě." Master's thesis, 2012. http://www.nusl.cz/ntk/nusl-307787.
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Anilazine (4,6-dichloro-N-(2-chlorophenyl)-1,3,5-triazin-2-amine) is a fungicide from a group of triazine pesticides. These have been very widely used but for their toxicity for water environment they are being cancelled. Use of anilazine is not allowed anymore in the European Union. However, traces of its residues are able to find in environmental samples. The diploma thesis deals with determination of anilazine using silver solid amalgam electrode modified by mercury meniscus (m-AgSAE). Differential pulse voltammetry was used. For the determination, an acidic solution is necessary. In the work Britton-Roninson buffer pH = 2 was used. This is because of electrochemical reduction of anilazine (and other triazines) which is started by protonization of heterocycle ring. Anilazine exhibits one single well-defined peak, the potential of the peak was about Ep = -827 mV (vs. 3 mol l-1 argentochloride electrode). The limit of quantification achieved in surface water was 2 µmol.l-1. Other two possibilities of getting lower limit of quantification were examined - Adsorptive Stripping Voltammetry (AdSV) and preconcentration by Solid Phase Extraction (SPE). Using AdSV the limit of quantification LQ = 0,5 µmol.l-1. Conditions of adsorption were as following: Eacc = -100 mV, tacc = 60 s. For SPE, 200-mg columns...
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Maška, Jan. "Elektrochemické stanovení Fomesafenu." Master's thesis, 2013. http://www.nusl.cz/ntk/nusl-323466.
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The submitted work deals with the application of voltammetric determination of Fomesafen using non-traditional mercury meniscus modified silver solid amalgam electrode on model samples of Fomesafen in real aqueous matrices of drinking and river water. This method of measurement has been developed and optimized in my bachelor thesis, which the diploma thesis is related to. Fomesafen belongs to a group of herbicides used on a mass scale in the late 20th century in the USA and in many countries around the world still used even today. Among its side effects according to the EPA include, among others, potential carcinogenicity to humans and confirmed carcinogenicity to some mammals (such as rats) which led to a legislative regulation on its use in many countries around the world including the USA, the European Union and many others. Silver solid amalgam electrode has been developed with the intention to limit the use of mercury in accordance with new legislation of the European Union and the concept of green analytical chemistry. Despite the low levels of mercury mainly bound in the form of virtually harmless silver amalgam electrode retains very similar electrochemical properties with proven mercury electrodes. As part of the thesis, direct determination of a number of partial extraction of Fomesafen...
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Yosypchuk, Oksana. "Voltametrická a amperometrická detekce genotoxických derivátů pyrenu pomocí bórem dopované diamantové filmové elektrody." Master's thesis, 2010. http://www.nusl.cz/ntk/nusl-296643.
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This thesis is concentrated on the optimization of conditions for determination of genotoxic environmental pollutants whitch belong to derivatives of polycyclic aromatic hydrocarbons − 1-nitropyrene (1-NP), 1-aminopyrene (1-AP) and 1-hydroxypyrene (1-HP). All three compounds were determined by differential pulse voltammetry (DPV) at boron-doped diamond film electrode in water-methanolic solutions. Further, 1-AP and 1-HP were determined in a model sample of urine. For this purpose, effective separative techniques such as solid phase extraction and high performance liquid chromatography with reverse phase and amperometric detection at above mentioned type of electrode were used. Limits of detection of all tested compounds in water-methanolic solutions are 9⋅10−8 −3⋅10−7 mol dm−3 using DPV and 1⋅10−8 mol dm−3 for 1-HP and 1-AP in model sample of urine determined by HPLC with amperometric detection.
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Houšková, Lucie. "Elektrochemické stanovení chlortoluronu na uhlíkové pastové elektrodě." Master's thesis, 2012. http://www.nusl.cz/ntk/nusl-310501.
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Chlortoluron is a herbicide from the group of substituted ureas and it is used for weed control in production of cereals and poppy. Substituted ureas are widely used but these substances are known for their high mobility in soil, persistence and contamination of underground water. Therefore, the development of analytical methods suitable for residual concentrations determination is necessary. This thesis deals with the determination of chlortoluron using carbon paste electrode (CPE) by the methods of differential pulse voltammetry and high-performance liquid chromatography with electrochemical (HPLC-ED) and spectrophotometric (HPLC-UV) detection. The aim of the work was to find optimal conditions suitable for chlortoluron determination. Further, the possibility of using miniaturized carbon paste electrode (mCPE) and usability of tested methods for determination of chlortoluron in model samples of river water and soil were studied. Concentration dependences in deionized water were measured by the method of DPV in the Britton-Robinson (BR) buffer (pH = 3) and methanol (10 %, v/v). The limit of detection was 3,7∙10-7 mol∙dm-3 in the case of CPE and 8,7∙10-8 mol∙dm-3 in the case of mCPE. Also, concentration dependences were measured using HPLC with mobile phase containing BR buffer (pH = 4) and...
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Gajdár, Július. "Využití antimonových filmových elektrod pro stanovení pesticidu trifluralin." Master's thesis, 2015. http://www.nusl.cz/ntk/nusl-339509.
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Antimony film electrode was studied for the use in a voltammetric analysis of organic compounds. The substance chosen as an analyte was trifluralin, which is used as a pesticide. The comparison of different substrate electrodes was carried out between five electrodes, which were gold, silver, copper, polished amalgam and glassy carbon electrode (GCE). Best performance was observed on antimony film glassy carbon electrode (SbFGCE). It provided higher sensitivity and lower limit of quantification in comparison with bare GCE. The antimony film was stable and it provided good reproducibility (RSD = 5.2 %). Parameters of an electrochemical preparation of SbFGCE were optimized. Conditions for determination of concentration of trifluralin were optimized on newly prepared SbFGCE. The best conditions were in a solution of methanol and 0.1 M hydrochloric acid in 1:1 ratio measured by differential pulse voltammetry. The limit of quantification was determined as 1.2·10-6 mol·l-1 . A direct voltammetric measurement on SbFGCE was carried out in a model river sample. Lower limits of quantification were achieved with solid phase extraction (SPE). Recovery values were 86 ± 8 % in deionized water with a preconcentration factor of 125. The limit of quantification was lowered to value 1.1·10-8 mol·l-1 . The extraction...
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Krejčová, Zuzana. "Voltametrické studium interakce genotoxického 2-nitrofluorenu s DNA na visící rtuťové kapkové elektrodě." Master's thesis, 2011. http://www.nusl.cz/ntk/nusl-297579.
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In this Diploma Thesis, an interaction of genotoxic environmental pollutant 2-nitrofluorene with a double-stranded calf thymus DNA has been studied using a hanging mercury drop electrode (HMDE) as an electrochemical sensor. Two types of DNA damage were investigated and electrochemically detected (using cyclic voltammetry and differential pulse voltammetry): (i) The DNA damage caused by the direct interaction with 2-nitrofluorene and (ii) the DNA damage caused by short-lived radicals generated by the electrochemical reduction of the nitro group in 2-nitrofluorene. For the study of direct interaction, HMDE was modified by DNA and the interaction of DNA with 2-nitrofluorene was studied, after their incubation, right at the HMDE surface (adsorptive transfer stripping technique) or the DNA was preincubated with 2-nitrofluorene and, subsequently, the interaction was studied voltammetrically (DNA titration technique). Using both detection techniques, the formation of DNA - 2-nitrofluorene complex was observed and the mutual interaction was interpreted as an intercalation between the DNA base pairs, although such interaction was not clearly confirmed by UV-visible absorption spectroscopy. An electrostatic binding of 2-nitrofluorene on DNA sugar-phosphate backbone was partially formed at low concentrations of...
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Prchal, Vít. "Využití chemicky modifikovaných elektrod při voltametrické analýze nitroaromatických sloučenin." Master's thesis, 2011. http://www.nusl.cz/ntk/nusl-313237.
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The main objective of this Diploma Thesis is studying the possibility of detection of nitro derivatives of aromatic hydrocarbons by using chemically modified working electrodes in electrochemical analysis. Compounds analyzed in this work were 1-nitronaphthalene and 6- nitrochrysene - these compounds were chosen on previous experience with surface modified working electrodes (the chemical/physical properties of these substances). All the analyses were performed by using differential pulse voltammetry (DPV) on hanging mercury drop electrode (HMDE) in classic three-electrode system. The original premise of chemical modification of electrode surface is the change of its selectivity towards different compounds - meaning the change of the electrochemical response. The modification agent used in this thesis is 1-octanethiol. Its thiol group offers great potential of strong interaction with the metal surface of the mercury electrode. Voltammetric responses of both compounds were recorded in acidic, neutral and basic solutions (pH=2, pH=7, pH=12) including the responses when the electrode surface was modified. Next objective was the optimization of the modification procedure itself (transferring of the mercury drop from one media to another without damaging or tearing it off from the capillary orifice)....
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Chládková, Barbora. "Voltametrické stanovení 5-nitrobenzimidazolu za využití netradičních elektrodových materiálů." Master's thesis, 2012. http://www.nusl.cz/ntk/nusl-307436.
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5 Abstract This Diploma Thesis is targeted on the determination of 5-nitrobenzimidazole (5-NBIA) using following techniques: DC voltammetry (DCV) and differential pulse voltammetry (DPV). As working electrodes, a silver amalgam paste electrode (AgA-PE), which was constructed for this determination in the form of a new prototype, a bismuth film electrode (BiFE), at which the optimum conditions for the deposition of the bismuth film at a suitable substrate (glassy carbon electrode and gold electrode were tested for this purpose) were initially optimized, and a glassy carbon electrode (GCE) were used. The optimum conditions for the voltammetric determination of 5-NBIA at the AgA-PE (in a medium of Britton-Robinson buffer (BR-buffer) of pH 7.0 for both DCV and DPV), at the BiFE with gold substrate (BR-buffer of pH 9.0 for both DCV and DPV; the film was deposited "ex situ" in a stirred plating solution (1000 mg L-1 Bi(III) solution in 0.1 mol L-1 acetate buffer of pH 4.5) for 300 s), and at the GCE (BR-buffer of pH 5,0 for both DCV and DPV). Under these conditions, calibration dependences were measured in the concentration ranges of 0.1 - 100 µmol L-1 (pro DCV a DPV na AgA-PE) and 1 - 100 µmol L-1 (pro DCV a DPV na BiFE a GCE), and the limits of quantification (LQs) were calculated for particular methods: LQ ≈...
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Karaová, Jana. "Voltametrické a amperometrické stanovení nitrofenolů pomocí borem dopované diamantové filmové elektrody." Doctoral thesis, 2018. http://www.nusl.cz/ntk/nusl-391379.
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Presented Ph.D. Thesis is focused on the use of the boron-doped diamond (BDD) electrodes for voltammetric and amperometric determination of selected nitrophenols: 2-nitrophenol (2NP), 4-nitrophenol (4NP), and 2,4-dinitrophenol (2,4DNP). These compounds are listed as "priority pollutants" by United States Environmental Protection Agency (US EPA) due to their negative impact on living organisms and are mainly used in agriculture as plant growth stimulators. BDD electrodes are used for determination of wide range of electrochemically both reducible and oxidisable organic compounds and have become a popular electrode material thanks to its commercial availability and excellent mechanical and electrochemical properties. A differential pulse voltammetric method was developed for the determination of 2NP, 4NP and 2,4DNP at a BDD film electrode using electrochemical reduction and of 4NP and 2,4DNP using electrochemical oxidation. The method was successfully applied for the direct determination of these compounds in drinking and river water in the concentration range from 4×10-7 to 2×10-5 mol.L-1 . To improve the limit of quantification, a preconcentration by solid phase extraction from 100 mL (drinking and river water) and 1000 mL (drinking water) of water samples was used with limit of determination...
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Němečková, Anna. "Voltametrické a amperometrické stanovení homovanilové, vanilmandlové a 5-hydroxy-3-indoloctové kyseliny." Doctoral thesis, 2020. http://www.nusl.cz/ntk/nusl-434498.
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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,...