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Compatibility of determination of antimony by UV-photochemical generation of volatile compounds and atomic fluorescence spectrometry with potential matrix components
Klečková, Adéla ; Červený, Václav (advisor) ; Nováková, Eliška (referee)
The root of this bachelor work is UV-photochemical generation (UV-PVG) of volatile substances of antimony. Problematics, with which we deal, are potential interferences, which can affect measurement. As model interferents when considering future speciation analysis of antimony using HPLC-UV-PVG-AFS were chosen acetonitrile, methanol, ethanol, L-cysteine and 2-mercaptoethanol. Detection was progressed using atomic fluorescence spectrometry (AFS). L-cysteine muffled the response. Methanol and ethanol were behaving alike. They were increasing and lowering the peaks in waves, when only at the highest concentration they completely disappeared. Acetonitrile was proved to be the most interesting one thanks to its specifical behaviour, which started to show off in higher concentration. 2-mercaptoethanol had in smaller amount similar interference properties as acetonitrile.
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Analysis of products of cardanol metathesis by HPLC-MS/MS method
Flenerová, Zuzana ; Čabala, Radomír (advisor) ; Vrkoslav, Vladimír (referee)
Cardanols are more and more used in the industry of polymers, resins, coatings, friction materials, etc. At right conditions, these lipid-like chemicals can undergo metathesis reaction. The main aim of the diploma thesis is an analysis of products of cardanol metathesis by HPLC-MS/MS. Standard 3,3'-hexadec-8-en-1,16-diyldiphenol, one of the main products of cardanol metathesis, was prepared for quantitative HPLC analysis. The standard was prepared in two steps. The first step was cardanol ethenolysis to give 3-(non-8-enyl)phenol. The second step was self-metathesis of 3-(non-8- enyl)phenol to give 3,3'-hexadec-8-en-1,16-diyldiphenol. The standard was characterised by HPLC/MS, MS/MS, EI-MS, UV/VIS, IR, Raman a NMR spectroscopy. The second part of the thesis is dedicated to the study of a mechanism of double-bond localization method in long chain hydrocarbons by acetonitrile APCI-MS. The formation of adducts [M + 55]+ , which are the key substances of this method, was studied using simple alkene models by MS and MS/MS. At the end, the structure and the mechanism of the formation of adducts [M + 55]+ were suggested. Key words: Cardanol, olefin metathesis, HPLC-MS, double-bond localization, APCI, acetonitrile
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Analysis of products of cardanol metathesis by HPLC-MS/MS method
Flenerová, Zuzana ; Čabala, Radomír (advisor) ; Vrkoslav, Vladimír (referee)
Cardanols are more and more used in the industry of polymers, resins, coatings, friction materials, etc. At right conditions, these lipid-like chemicals can undergo metathesis reaction. The main aim of the diploma thesis is an analysis of products of cardanol metathesis by HPLC-MS/MS. Standard 3,3'-hexadec-8-en-1,16-diyldiphenol, one of the main products of cardanol metathesis, was prepared for quantitative HPLC analysis. The standard was prepared in two steps. The first step was cardanol ethenolysis to give 3-(non-8-enyl)phenol. The second step was self-metathesis of 3-(non-8- enyl)phenol to give 3,3'-hexadec-8-en-1,16-diyldiphenol. The standard was characterised by HPLC/MS, MS/MS, EI-MS, UV/VIS, IR, Raman a NMR spectroscopy. The second part of the thesis is dedicated to the study of a mechanism of double-bond localization method in long chain hydrocarbons by acetonitrile APCI-MS. The formation of adducts [M + 55]+ , which are the key substances of this method, was studied using simple alkene models by MS and MS/MS. At the end, the structure and the mechanism of the formation of adducts [M + 55]+ were suggested. Key words: Cardanol, olefin metathesis, HPLC-MS, double-bond localization, APCI, acetonitrile
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