National Repository of Grey Literature 8 records found  Search took 0.00 seconds. 
Analysis of germanium in food
Musilová, Petra ; Moos, Martin (referee) ; Diviš, Pavel (advisor)
This bachelor‘s thesis deals with chemical, physical and medical characteristics of germanium. It also describes suitable analytical methods for determination of germanium.
Tin and his species in the environment
Bušinová, Markéta ; Moos, Martin (referee) ; Doležalová Weissmannová, Helena (advisor)
Presented bachelor thesis is background research on tin and his species in the environment. Mainly deals with the effects of inorganic and organic compounds of tin on elements of environment. The work resumes accessible information about properties of tin and his compounds, entry of tin and his compounds into the elements of environment, cycle and occurrence of tin speciation in water, soils, sediments and biological materials.
Preconcentration Techniques for Determination of Uranium Using the Modified Sorbents.
Moos, Martin ; Řehůřková, Irena (referee) ; Kanický, Viktor (referee) ; Kráčmar, Stanislav (referee) ; Sommer, Lumír (advisor)
The work has been focused on the preconcentration techniques for determination of uranium on the modified sorbent, with the final use of ICP-OES and ICP-MS. First ICP-OES at a wavelength of 385.958 nm was used for determination of uranium. Parameters were optimized and the effect of mineral acids (HCl, HNO3), tensides (Septonex, Ajatin) and organic reagents like (4-(2-pyridylazo)resorcinol, ammonium pyrrolidinedithiocarbamate, 8-hydroxyquinoline-5-sulphonic acid and 1,2-dihydroxyanthraquinone-3-sulphonic acid) was observed. For ICP-MS an isotope 238U was chosen. As an internal standard 209Bi (200 ?g•l-1) was used. Modified silica gel was used (Silicagel tethered with C18, C8 alkyls and phenyl) and two types of Amberlite XAD 4 and XAD 16 for the preconcentration of uranium (VI). Commercially produced Amberlite was modified as follows: Drying at 100 °C (24 hours), milled, minced sorbent was selected and fractionated to particles size ranging from 0.32 to 0.63 ?m and finally activated in methanol. The deionised water and Septonex (5•10-3 mol•l-1) at pH 8 were used for Amberlite conditioning. The optimal sorption of uranium (VI) proceeded at pH 8 in the presence of 4-(2-pyridylazo)resorcinol or ammonium pyrrolidinedithiocarbamate with Amberlite XAD-16 moreover with 1,2-dihydroxyanthraquinone-3-sulphonic acid. All organic reagents have mass concentration five time larger than uranium . For the elution of uranium the mixture of 1 mol•l-1 HNO3 with acetone (ratio of 1:1) was used. Acetone was evaporated and the final analysis performed using ICP-OES. The preconcentration of uranium (VI) using Silicagel-C18 conditioning was performed with ethanol, deionised water and Zephyraminu (5•10-4 mol•l-1) at pH 8. For the Silica-C8 and Silicagel-Phenyl the same conditioning procedure without zephyramin was used. Silica-C18 had the highest sorption efficiency with 1,2-dihydroxyanthraquinone-3-sulphonic acid, Silicagel-C8 with ammonium pyrrolidinedithiocarbamate and Silicagel-Phenyl with 8-hydroxyquinoline-5-sulfonic acid, all organic reagents have mass concentration five time larger than uranium concentration. As an optimal elution mixture acetone and ethanol (ratio of 1:1) in the presence of 1 mol•l-1 HCl was evaluated. Acetone and ethanol was evaporated and the final analysis was performed using ICP-MS. Silicagel-C18 was evaluate as the most effective in the presence of zephyramin and 1,2-dihydroxyanthraquinone-3-sulphonic acid. Sorption was also tested in the presence of 20 ?g•l-1 microelements (Be, V, Co, Ni, Y, Pb, Th, Cd) and in the presence of a defined concentrations of K, Na, Ca, Mg, Al and Fe. Direct analysis of uranium was carried out on samples of water from the river Ploucnice and Turonian aquifers containing uranium, 3,5 and 19,3 ?g•l-1. Different type of water required preconcentration of uranium (VI) on Silica-C18 in the presence of 1,2-dihydroxyanthraquinone-3-sulphonic acid and zephyramin. The analysis results gave statistically satisfactory results, which were confirmed using standard addition of 20 ?g•l-1.
Preconcentration Techniques for Determination of Uranium Using the Modified Sorbents.
Moos, Martin ; Řehůřková, Irena (referee) ; Kanický, Viktor (referee) ; Kráčmar, Stanislav (referee) ; Sommer, Lumír (advisor)
The work has been focused on the preconcentration techniques for determination of uranium on the modified sorbent, with the final use of ICP-OES and ICP-MS. First ICP-OES at a wavelength of 385.958 nm was used for determination of uranium. Parameters were optimized and the effect of mineral acids (HCl, HNO3), tensides (Septonex, Ajatin) and organic reagents like (4-(2-pyridylazo)resorcinol, ammonium pyrrolidinedithiocarbamate, 8-hydroxyquinoline-5-sulphonic acid and 1,2-dihydroxyanthraquinone-3-sulphonic acid) was observed. For ICP-MS an isotope 238U was chosen. As an internal standard 209Bi (200 ?g•l-1) was used. Modified silica gel was used (Silicagel tethered with C18, C8 alkyls and phenyl) and two types of Amberlite XAD 4 and XAD 16 for the preconcentration of uranium (VI). Commercially produced Amberlite was modified as follows: Drying at 100 °C (24 hours), milled, minced sorbent was selected and fractionated to particles size ranging from 0.32 to 0.63 ?m and finally activated in methanol. The deionised water and Septonex (5•10-3 mol•l-1) at pH 8 were used for Amberlite conditioning. The optimal sorption of uranium (VI) proceeded at pH 8 in the presence of 4-(2-pyridylazo)resorcinol or ammonium pyrrolidinedithiocarbamate with Amberlite XAD-16 moreover with 1,2-dihydroxyanthraquinone-3-sulphonic acid. All organic reagents have mass concentration five time larger than uranium . For the elution of uranium the mixture of 1 mol•l-1 HNO3 with acetone (ratio of 1:1) was used. Acetone was evaporated and the final analysis performed using ICP-OES. The preconcentration of uranium (VI) using Silicagel-C18 conditioning was performed with ethanol, deionised water and Zephyraminu (5•10-4 mol•l-1) at pH 8. For the Silica-C8 and Silicagel-Phenyl the same conditioning procedure without zephyramin was used. Silica-C18 had the highest sorption efficiency with 1,2-dihydroxyanthraquinone-3-sulphonic acid, Silicagel-C8 with ammonium pyrrolidinedithiocarbamate and Silicagel-Phenyl with 8-hydroxyquinoline-5-sulfonic acid, all organic reagents have mass concentration five time larger than uranium concentration. As an optimal elution mixture acetone and ethanol (ratio of 1:1) in the presence of 1 mol•l-1 HCl was evaluated. Acetone and ethanol was evaporated and the final analysis was performed using ICP-MS. Silicagel-C18 was evaluate as the most effective in the presence of zephyramin and 1,2-dihydroxyanthraquinone-3-sulphonic acid. Sorption was also tested in the presence of 20 ?g•l-1 microelements (Be, V, Co, Ni, Y, Pb, Th, Cd) and in the presence of a defined concentrations of K, Na, Ca, Mg, Al and Fe. Direct analysis of uranium was carried out on samples of water from the river Ploucnice and Turonian aquifers containing uranium, 3,5 and 19,3 ?g•l-1. Different type of water required preconcentration of uranium (VI) on Silica-C18 in the presence of 1,2-dihydroxyanthraquinone-3-sulphonic acid and zephyramin. The analysis results gave statistically satisfactory results, which were confirmed using standard addition of 20 ?g•l-1.
Tin and his species in the environment
Bušinová, Markéta ; Moos, Martin (referee) ; Doležalová Weissmannová, Helena (advisor)
Presented bachelor thesis is background research on tin and his species in the environment. Mainly deals with the effects of inorganic and organic compounds of tin on elements of environment. The work resumes accessible information about properties of tin and his compounds, entry of tin and his compounds into the elements of environment, cycle and occurrence of tin speciation in water, soils, sediments and biological materials.
Analysis of germanium in food
Musilová, Petra ; Moos, Martin (referee) ; Diviš, Pavel (advisor)
This bachelor‘s thesis deals with chemical, physical and medical characteristics of germanium. It also describes suitable analytical methods for determination of germanium.
The relationships of soil CO2 flux with selected Norway spruce root parameters and sterol content in the soil
Holub, Filip ; Fabiánek, Tomáš ; Večeřová, Kristýna ; Moos, Martin ; Oravec, Michal ; Tříska, Jan ; Marková, I. ; Edwards, Magda ; Cudlín, Pavel
The flow of CO2 from the soil is a very important part of the carbon cycle in an ecosystem. The aim of our work was to determine how roots and rhizospheric fungi contribute to CO2 flux from the soil. Preliminary results from two years of research are presented. The research on how root biomass as well as ergosterol and phytosterol contents in roots and soil affected CO2 flux from the soil was conducted in a 108-year-old Norway spruce (Picea abies (L.) Karst.) forest in the Drahany Highlands during 2010 and 2011. CO2 flow was measured using a LI-8100 portable closed gasometric system (Li-Cor, USA). The dry weight and volume of individual root categories (< 1 mm, 1–2 mm, 2–5 mm, > 5 mm), C and N contents in the roots, as well as ergosterol, β-sitosterol, and campesterol contents in the soil and roots were determined from root-containing soil samples located in the circular measurement chamber. In addition, sterol content was determined in the soil only. Our soil respiration results correspond with the findings of Buchman (2000) who found respiration values between 5–7 μmol CO2 m−2 s−1 in a 111-year-old spruce forest. A significant influence on soil respiration was proven only for sitosterol content in the soil. The relationships among soil CO2 flux, root characteristics, and nitrogen and sterol contents in the roots and soil are discussed.
Occurence of lignans in environmental waters
Tříska, Jan ; Moos, Martin ; Marešová, I. ; Vrchotová, Naděžda
The content of lignans, especially hydroxymatairesinol (HMR) was investigated in different types of natural waters from the environment. Collected water samples were extracted with methyl tert. butylether, derivatized and analysed by means of GC-MS. HMR was found in different amount in all water samples beside the other lignans.

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