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Hormones in waste waters
Petrušová, Pavlína ; Vávrová, Milada (referee) ; Čáslavský, Josef (advisor)
This bachelor thesis gives the overview of waste water contaminants of steroid hormones type. A short description of these compounds and of their physical-chemical properties is given and sources of these substances in the environment are characterized, as well as their impact on organisms The fate of these compounds and methods used for their isolation from environmental compartments methods of their final analysis are characterized.
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Multicomponental Preconcentration of As, Sb, Se and Te on Modified Silica, Their Determination by ICP-AES (ICP-MS) and Application for Waters
Urbánková, Kristýna ; Řehůřková, Irena (referee) ; Kanický, Viktor (referee) ; Ventura, Karel (referee) ; Sommer, Lumír (advisor)
The determination of inorganic speciations of arsenic, antimony, selenium and tellurium in natural waters demands often separation and preconcentration. Solid phase extraction is a very effective method for these purposes. In this paper the separation and preconcentration of these microelements is realised on the basis of modified silica Separon SGX C18, SGX C8, SGX CN, SGX NH2, SGX Phenyl and strongly basic anion Exchanger SGX AX. The sorption was provided in the presence of cationic surfactants such as benzyldimethyl dodecylammonium bromide (Ajatin), benzyldimethyltetradecylammonium chloride (Zephyramine), 1-ethoxycarbonylpentadecyltrimetrhylammonium bromide (Septonex) and selected complexing agents 4-(2-pyridylazo)resorcinol (PAR), 8-hydroxyquinoline-5-sulphonic acide (8-HQS), 1,2-dihydroxybenzene (PYR), amonium 1-pyrrolidinecarbodithioate (APDC), sodium diethyldithiocarbamate (DTC) or thiourea(Thur). The interactions of the formed ion associate with the sorbent shows a complicated character which has not been cleared as yet. The previous conditioning of the sorbent plays an outstanding role. Thus, the sorption efficiency was studied in the presence and absence of surfactant and of selected organic complexing agents. Moreover, the influence of pH of the sorbed solution as well as the speed and the volume of the solution running through the sorbent and the type and volume of the eluent on the resulting sorption efficiency was evaluated. The sorption was successfully carried out from 50-1000 ml of solution which allows the 100 fold increase of the preconcentration factor and the determination of the microelements in g.l-1 instead of mg.l-1 by using the common ICP-AES. The influence of macroelements occurring in waters as well as B, Be, Bi, Cd, Co, Cr, Cu, Mn, Mo, Ni, Pb, Sr, Ti, V and Zn in comparable concentrations involve less than 5% error. After the quantitative elution of microelements, the organic solvents were evaporated under IR lamps prior to the determination by ICP-AES and |ICP-MS. The conditions for the direct determination of arsenic, antimony, selenium and tellurium in g.l-1 with ICP-MS were also described in detail in the absence and presence of internal standards Ge and Bi. However, even in this case the preconcentration on silica in the presence of surfactant and selected organic complexants was also tested. When the sorption was followed from 500 ml a 50 fold enrichment factor is reached and the sensitivity for the microelements is improved. The direct determination and the sorption of microelements were applied on synthetic and real waters (dirinking, surface, mineral and sea waters). Instrumental and practical detection limits for various water samples were evaluated according to IUPAC. The results from 1000 ml solution of real waters after sorption on modified silica and the final determination of microelements with ICP-AES were compared with those from ICP-MS without sorption using the method of standards addition in the presence of suitable internal standards. By comparison of results for synthetic and real water samples the error of the determination of microelements was evaluated.
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The use of SPE methods for determination of ultratrace concentrations of platinum metals in environmental matrices
Ježek, Stanislav ; Zlámalová Gargošová, Helena (referee) ; Gregor, Tomáš (referee) ; Komendová, Renata (advisor)
This dissertation is focused on the study of sorption techniques for the determination of platinum and palladium on modified solid sorbents and ion exchangers. The final determination was made using atomic absorption spectrometry with electrothermal atomization (ET-AAS). Six modified sorbents were selected for the sorption study. Four modified non-polar silica gels were studied and two sorbents were based on styrene divinylbenzene copolymer. Furthermore, three cation exchange resins and three anion exchange resins were studied. The sorption efficiency of platinum and palladium was studied with modified sorbents and anion exchange resins. Furthermore, the influence of interfering elements (Fe, Cu, Zn, Pb, K, Na, Ca and Mg). Another parameter for evaluating the effectiveness of sorbents is the volume of the elution mixture required for effective elution of platinum and palladium from the sorbents. Based on the results, a sorbent was selected for the preconcentration of platinum and palladium from real environmental samples from the environment. The study of the concentration of platinum and palladium in environmental components is divided into two parts. The first part compares two cities with different sizes and vehicle concentrations. It is a regional capital in the Czech Republic – Jihlava and the capital of Austria – Vienna. For soil matrix sampling, locations near frequent traffic junctions were selected. In Jihlava, the concentration of platinum ranged from 16.93 to 38.72 ng.g-1 and for palladium from 2.705 to 8.452 ng.g-1. In Vienna, the detected concentrations were higher. Platinum concentrations ranged from 39.22 ng.g-1 to 159.2 ng.g-1 and for palladium from 18.45 ng.g-1 to 98.21 ng.g-1. The second part was focused on the busiest traffic junction in the Czech Republic - the D1 highway, focusing on the section near the Švihov water reservoir, which serves as one of the main sources of drinking water for the capital of the Czech Republic - Prague. Rain retention tanks - "lapolas" - are installed in this section. A soil sample was always taken in the vicinity of these lapolas, and from the lapolas the sediment in the reservoir and settled water at the outlet from the reservoir. These rain retention tanks proved to be suitable places for monitoring pollutants from automobile traffic.
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Modular design for in-atomizer preconcentration of hydride forming elements with AAS detection
Novák, Petr ; Kratzer, Jan (advisor) ; Korunová, Vlasta (referee)
Modular design of hydride trap-and-atomizer device for AAS is constructed and tested. Modular design enables to test different preconcentration surfaces easily. Efficient in- atomizer preconcentration allows to reach detection limits of hydride forming elements at ultratrace levels. Bismuth and arsenic were chosen as model analytes and their preconcentration efficiencies were quantified employing quartz and sapphire as preconcentration surfaces. The results reached in the modular design were compared to those found previously in the compact quartz trap-and-atomizer device. The performance of the modular design is fully comparable with that of compact trap-and-atomizer design. Modular design can thus be employed for testing of novel preconcentration surfaces.
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A novel AAS atomizer based on a dielectric barrier plasma discharge
Novák, Petr ; Kratzer, Jan (advisor) ; Kanický, Viktor (referee)
Atomization of arsine in a novel hydride atomizer for atomic absorption spectrometry (HG-AAS) was thoroughly optimized. This plasma atomizer is based on a dielectric barrier discharge (DBD). Sensitivity and detection limit reached 0.48 s ng-1 As and 0.16 ng ml-1 As, respectively, under optimum atomization conditions (Ar discharge using a flow rate of 60 ml min-1 Ar, DBD power 17 W). Analytical figures of merit reached in DBD are comparable to those found in an externally heated quartz tube multiatomizer (MMQTA) that was chosen as a model of conventional approach to hydride atomization in HG-AAS. An extent of interferences (Se, Sb, Bi) during As determination was investigated comparing both MMQTA and DBD atomizers. The later one was found to be more resistant towards interferences. A simple preconcentration of As in a DBD atomizer was reached after oxygen introduction into the Ar plasma in the DBD resulting in analyte retention in the atomizer followed by its volatilization once the oxygen flow is switched off. Preconcentration efficiency of 100 % was reached and detection limit improvement by a factor of ten was achieved (0.01 ng ml-1 As, preconcentration period 300 s).
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Speciation analysis of mercury in liquid and gaseous samples
Žídek, Radek ; Kratzer, Jan (advisor) ; Spěváčková, Věra (referee)
Generation efficiency of four mercury species, namely elemental mercury and hydrides of methyl-, ethyl- and phenylmercury from liquid samples was quantified. The species chemically generated were quantitatively trapped on a gold-coated amalgamator to be subsequently determined by AMA-254 technique. Three types of construction of volatile species generators were compared. Generation effciciency among the species was comparable, fluctuating around 60% in the conventional flow injection generator equipped with a gas liquid separator with forced outlet. Better results were reached for elemental mercury and methylmercury hydride in an automated batch generator system. Generation efficiency was higher than 90% for these two species and between 60 to 80% for ethyl- and phenylmercury hydrides, respectively. Speciation analysis of elemental mercury and sublimate in gaseous samples was optimized. These two species dominate in flue gases produced during coal combustion or waste incineration. Combination of two sorbent tubes packed with alumina and gold-coated alumina enables selective and quantitative retention of both species. Sublimate is trapped on a column packed with alumina while elemental mercury is retained on gold-coated alumina. The capacity of both sorbents was investigated as well as the effect of...
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Preconcentration of hydride forming elements in quartz trap in connection with ICP-MS
Kašpar, Miroslav ; Matoušek, Tomáš (advisor) ; Rychlovský, Petr (referee)
Charles Uviversity in Prague Faculty of Science Department of Analytical Chemistry Student: Miroslav Kašpar Supervisor: RNDr. Tomáš Matoušek, Ph.D. Name of Thesis: Preconcentration of hydride forming elements in quartz trap with ICP-MS detection The aim of this thesis are pilot experiments employing quartz trap (QT) for preconcentration of hydride forming elements and their subsequent detection by inductively coupled plasma mass spectrometry (HG-QT-ICP-MS). Arsenic and antimony were chosen as model analytes. Preconcentration efficiency on quartz surface was studied in a trap, which was integrated into an interface between spray chamber and plasma torch. We have identified a critical loss of analyte during transportation, instability of the plasma due to sudden change of gas composition, poor repeatability and very quick release of Sb from the trap resulting in difficult quantification of Sb signal. Despite the efforts to resolve these experimental problems, so far we were unable to achieve improvements in analytical parameters compared to standard analytical methods. Keywords: Preconcentration, quartz trap, mass spectrometry with inductively coupled plasma, hydride generation, arsenic, antimony
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Selenium determination by HG-AAS with preconcentration and atomization in a dielectric barrier plasma discharge
Duben, Ondřej ; Kratzer, Jan (advisor) ; Rychlovský, Petr (referee)
The aim of this thesis was to optimize atomization conditions for selenium hydride in a novel plasma atomizer based on dielectric barrier discharge (DBD) using atomic absorption spectrometry as a detector. Analytical characteristics have been subsequently determined and compared to those reached in a conventional externally heated quartz tube atomizer which was replaced by a sofisticated design of a multiatomizer (MMQTA) in this work. The limit of detection reached in DBD (0,24 ng ml−1 Se) is slightly worse to that observed in MMQTA (0,15 ng ml−1 Se). On the contrary, slightly better resistance towards interferences of Sb, Bi and As was observed in DBD atomizer in comparison with MMQTA. Possibility of selenium preconcentration in a DBD atomizer was studied reaching an overall preconcentration efficiency of 75 ± 5%. The detection limit in a preconcentration mode employing preconcentration period of 300 s has reached 0,012 ng ml−1 Se. Key words: hydride generation atomic absorption spectrometry, dielectric barrier discharge, hydride atomization, hydride trapping, selenium
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A novel AAS atomizer based on a dielectric barrier plasma discharge
Novák, Petr ; Kratzer, Jan (advisor) ; Kanický, Viktor (referee)
Atomization of arsine in a novel hydride atomizer for atomic absorption spectrometry (HG-AAS) was thoroughly optimized. This plasma atomizer is based on a dielectric barrier discharge (DBD). Sensitivity and detection limit reached 0.48 s ng-1 As and 0.16 ng ml-1 As, respectively, under optimum atomization conditions (Ar discharge using a flow rate of 60 ml min-1 Ar, DBD power 17 W). Analytical figures of merit reached in DBD are comparable to those found in an externally heated quartz tube multiatomizer (MMQTA) that was chosen as a model of conventional approach to hydride atomization in HG-AAS. An extent of interferences (Se, Sb, Bi) during As determination was investigated comparing both MMQTA and DBD atomizers. The later one was found to be more resistant towards interferences. A simple preconcentration of As in a DBD atomizer was reached after oxygen introduction into the Ar plasma in the DBD resulting in analyte retention in the atomizer followed by its volatilization once the oxygen flow is switched off. Preconcentration efficiency of 100 % was reached and detection limit improvement by a factor of ten was achieved (0.01 ng ml-1 As, preconcentration period 300 s).
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Modular design for in-atomizer preconcentration of hydride forming elements with AAS detection
Novák, Petr ; Kratzer, Jan (advisor) ; Korunová, Vlasta (referee)
Modular design of hydride trap-and-atomizer device for AAS is constructed and tested. Modular design enables to test different preconcentration surfaces easily. Efficient in- atomizer preconcentration allows to reach detection limits of hydride forming elements at ultratrace levels. Bismuth and arsenic were chosen as model analytes and their preconcentration efficiencies were quantified employing quartz and sapphire as preconcentration surfaces. The results reached in the modular design were compared to those found previously in the compact quartz trap-and-atomizer device. The performance of the modular design is fully comparable with that of compact trap-and-atomizer design. Modular design can thus be employed for testing of novel preconcentration surfaces.
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