Neste projeto foram abordados procedimentos analíticos para extração, separação e identificação de espécies de arsênio encontradas normalmente em quantidades de traços e ultra-traços em amostras biológicas e ambientais. Entre as amostras alvo deste estudo, teve-se alimentos de origem marinha como por exemplo camarão. Foi avaliada a estabilidade das espécies de arsênio nas soluções geradas pelos processos de extração. Para separação das espécies inorgânicas (arsenito e arsenato), metiladas (ácidos mono e dimetil arsênio) e orgânicas (arsenobetaina) empregaram-se as técnicas eletroforese capilar (CE) e cromatografia líquida (LC). Os sistemas de separação para a determinação das espécies de arsênio foram acoplados com os espectrômetros massas (ICP-MS), e de fluorescência atômica (AFS). Os sistemas acoplados apresentaram resolução e sensibilidade na determinação das espécies de arsênio nas amostras estudadas neste trabalho. A extração com água de espécies de As utilizando-se banho de ultra-som apresentou eficiência acima de 78%. A estabilidade das espécies nas soluções padrão e nos extratos das amostras foi mantida por um período de até uma semana quando armazenadas em geladeira (+4°C). Visando uma política de química limpa, foi desenvolvida uma metodologia para evitar desperdiço preparando micro-volumes de amostras e soluções padrão, para especiação de arsênio por eletroforese capilar. Para tal se empregou um injetor seqüencial, também foi desenvolvido um dispositivo de injeção hidrodinâmica para eletroforese capilar. Além disto, as soluções residuais geradas durante a pesquisa analítica foram tratadas para a recuperação de arsênio e boro. A extração no ponto nuvem foi empregada para recuperar As entanto que a precipitação por mineralização hidrotérmica foi aplicada para a recuperação de B . A aplicação deste procedimento resultou na extração de 80% de arsênio e 75% de boro. Isto, permitiu converter grandes volumes de resíduos líquidos perigosos em um pequeno volume de resíduos sólidos / Analytical procedures for extraction, separation and identification of arsenic species at ultra-trace levels in biological and environmental samples were investigated. Stability studies of arsenic species in sample extracts and standard solutions were carried out. Separation of arsenite, arsenate, monomethylarsonic and dimethylarsinic acids and also arsenobetaine were carried out by capillary electrophoresis or liquid chromatography. Determination of the separated arsenic species was accomplished by coupling the separation techniques to inductively coupled plasma mass spectrometry (ICP-MS) or atomic fluorescence spectrometry (AFS). Satisfactory resolution and sensibility were achieved by the coupled systems described. Extraction efficiency better than78% were achieved with water in an ultrasonic bath at the laboratory temperature (23-27°C). Whereas, stability of species in solutions stored in refrigerator at +4°C was efficient for aperiod up to one week. Micro-volumes of standards and sample solutions mixed in a sequential injector were prepared for arsenic speciation by capillary electrophoresis, aiming green chemistry. A time controlled micro-volume injector device for hydrodinamic injections was also developed. Finally, waste solutions from arsenic speciation analysis in a system with hydride generation were treated for arsenic and boron removal. Cloud point extraction for recovery of arsenic and hydrothermal mineralization of boron by calcium hydroxide were employed. Satisfactory removal of 80% of arsenic and 75% of boron from waste solution was achieved. These procedures allowed to reduce volumes of hazardous waste solutions

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No description available.

O objetivo deste estudo foi avaliar parâmetros tais como, moagem, tamanho de partículas, homogeneidade, segregação, dissolução de amostras e amostragem de suspensão, visando o desenvolvimento de método para a determinação de Ir, Pd, Pt e Rh por espectrometria de emissão óptica com plasma indutivamente acoplado (ICP OES) em sílica mesoporosa para uso catalítico. Após a moagem em moinho eletrônico de almofariz e pistilo, a análise do tamanho e distribuição das partículas revelou que 89% das partículas apresentam tamanhos <100 &#181;m e 23% com tamanho <5 &#181;m. Na avaliação de segregação dos analitos na amostra, os resultados obtidos para amostra com moagem grosseira, indicaram que os elementos estão distribuídos de maneira heterogênea entre as frações. Entretanto, a moagem fina aumentou a homogeneidade e esta pode ser uma etapa importante e necessária no sentido de evitar segregação da amostra. A análise por difração e de Raios-X mostrou que não ocorreram reações mecanoquímicas durante a moagem e por fluorescência de Raios-X forneceu resultados discrepantes entre os laboratórios, o pode estar relacionado com a heterogeneidade que induziu erros de amostragem. A avaliação de desempenho do ICP OES foi feita a partir do estabelecimento de parâmetros de mérito como seletividade, repetibilidade, estabilidade, robutez e limite de detecção. Na otimização foram considerados os parâmetros potência, vazão de nebulização e vazão de gás auxiliar. Foi feito um estudo em solução aquosa e em meio da amostra para escolha das linhas de emissão dos elementos Ir, Pd, Pt, Rh e dos candidatos a padrões internos. Apesar dos bons resultados encontrados em solução aquosa, o aumento do sinal de fundo em meio da amostra restringiu a escolha dos comprimentos de onda. Para o estudo da dissolução das amostras foram avaliados quatro procedimentos em forno de micro-ondas com frasco fechado. Os melhores resultados foram obtidos com 150 mg de amostra, 6 mL de água régia e 210 ºC de aquecimento durante 60 min. As determinações por ICP OES usando padrões internos Ru para Pd, Yb para Pt e Dy para Rh foram aquelas que forneceram os resultados mais coerentes com aqueles obtidos por fluorescência de Raios-X. Nos estudos visando à introdução de amostra na forma de suspensão foram avaliados: a massa de amostra para o preparo da suspensão, o efeito da concentração de ácido nítrico e o uso de padrão interno na tentativa de corrigir erros de matriz. 60 mg de amostra com um volume final de 20 mL de ácido nítrico 0,5% (v v-1) foram os escolhidos. Entretanto, a determinação dos elementos via suspensão mostrou resultados muito inferiores aos valores de concentrações esperados. Irídio foi investigado somente para otimização de ICP OES porque a sílica mesoporosa para uso de catalisador automotivo tem não esse elemento em sua composição. / The aim of this study was to evaluate parameters such as grinding, particle size, homogeneity, segregation, sample dissolution and slurry sampling for method development for the determination of Ir, Pd, Pt and Rh in silica mesoporosa for catalyst using inductively coupled plasma optical emission spectrometry (ICP OES). After the grind in an electronic grider with mill and pistil, the analysis of the particle size distribution showed 89% of particles with sizes <100 &#181;m and 23% of particles with sizes <5&#181;m. The separation in different particle size fractions showed that the sample with coarse grind (as sent to the lab) is not homogenous for the elements in comparison with that submitted to grind. X-Ray Diffraction and X-Ray Fluorescence analysis did not showed chemical reactions during the grinding, however a discrepancy between results of different laboratories. The performance of ICP OES was made by using figures of merit such as selectivity, repeatability, stability, robustness and limit of detection. In the optimization of ICP OES power supply, nebulizer flow rate and auxiliary gas flow rate were considered. Studies were conducted in aqueous and in the sample solution to choose emission wavelengths for Ir, Pd, Pt, Rh and internal standard candidates. Despite the good results obtained in aqueous solution, increasing the background signal in sample media restricted the choice of the emission wavelengths. For sample dissolution four procedures using microwave oven with closed-vessel were evaluated. The best results were obtained with 150 mg of the sample, 6 mL of aqua-regia and 210 ºC of heating, during 60 min. Determinations by ICP OES using internal standards Ru for Pd, Yb for Pt, and Dy for Rh were those who provided more consistent results in comparison with those obtained by x-ray fluorescence. For slurry sampling introduction sush parameters were evaluated: the mass of sample to prepare the slurry, the effect of the nitric acid concentration and the use of internal standard to correct matrix effects. 60 mg of the sample with a final volume of 20 mL of nitric acid 0.5% (v v-1) were chosen. However, the determination of Pd, Pt and Rh via suspension showed concentrations below to those expected, as determined by ICP OES in solution. Iridium was investigated only for ICP OES optimization because the silica mesoporosa for automobile catalyst use have not this element in its composition.

Neste projeto foram abordados procedimentos analíticos para extração, separação e identificação de espécies de arsênio encontradas normalmente em quantidades de traços e ultra-traços em amostras biológicas e ambientais. Entre as amostras alvo deste estudo, teve-se alimentos de origem marinha como por exemplo camarão. Foi avaliada a estabilidade das espécies de arsênio nas soluções geradas pelos processos de extração. Para separação das espécies inorgânicas (arsenito e arsenato), metiladas (ácidos mono e dimetil arsênio) e orgânicas (arsenobetaina) empregaram-se as técnicas eletroforese capilar (CE) e cromatografia líquida (LC). Os sistemas de separação para a determinação das espécies de arsênio foram acoplados com os espectrômetros massas (ICP-MS), e de fluorescência atômica (AFS). Os sistemas acoplados apresentaram resolução e sensibilidade na determinação das espécies de arsênio nas amostras estudadas neste trabalho. A extração com água de espécies de As utilizando-se banho de ultra-som apresentou eficiência acima de 78%. A estabilidade das espécies nas soluções padrão e nos extratos das amostras foi mantida por um período de até uma semana quando armazenadas em geladeira (+4°C). Visando uma política de química limpa, foi desenvolvida uma metodologia para evitar desperdiço preparando micro-volumes de amostras e soluções padrão, para especiação de arsênio por eletroforese capilar. Para tal se empregou um injetor seqüencial, também foi desenvolvido um dispositivo de injeção hidrodinâmica para eletroforese capilar. Além disto, as soluções residuais geradas durante a pesquisa analítica foram tratadas para a recuperação de arsênio e boro. A extração no ponto nuvem foi empregada para recuperar As entanto que a precipitação por mineralização hidrotérmica foi aplicada para a recuperação de B . A aplicação deste procedimento resultou na extração de 80% de arsênio e 75% de boro. Isto, permitiu converter grandes volumes de resíduos líquidos perigosos em um pequeno volume de resíduos sólidos / Analytical procedures for extraction, separation and identification of arsenic species at ultra-trace levels in biological and environmental samples were investigated. Stability studies of arsenic species in sample extracts and standard solutions were carried out. Separation of arsenite, arsenate, monomethylarsonic and dimethylarsinic acids and also arsenobetaine were carried out by capillary electrophoresis or liquid chromatography. Determination of the separated arsenic species was accomplished by coupling the separation techniques to inductively coupled plasma mass spectrometry (ICP-MS) or atomic fluorescence spectrometry (AFS). Satisfactory resolution and sensibility were achieved by the coupled systems described. Extraction efficiency better than78% were achieved with water in an ultrasonic bath at the laboratory temperature (23-27°C). Whereas, stability of species in solutions stored in refrigerator at +4°C was efficient for aperiod up to one week. Micro-volumes of standards and sample solutions mixed in a sequential injector were prepared for arsenic speciation by capillary electrophoresis, aiming green chemistry. A time controlled micro-volume injector device for hydrodinamic injections was also developed. Finally, waste solutions from arsenic speciation analysis in a system with hydride generation were treated for arsenic and boron removal. Cloud point extraction for recovery of arsenic and hydrothermal mineralization of boron by calcium hydroxide were employed. Satisfactory removal of 80% of arsenic and 75% of boron from waste solution was achieved. These procedures allowed to reduce volumes of hazardous waste solutions

Le Pb est omniprésent dans les échantillons terrestres et sa relation avec ses ascendants radioactifs, l’U et le Th, en fait un marqueur de choix des processus géodynamiques.L’équipe lyonnaise de Janne Blichert-Toft et Francis Albarède a démontré, à travers une vaste compilation de données bibliographiques accompagnée de la production de nouvelles mesures, une correspondance entre la répartition des valeurs de composition isotopique du Pb dans la croûte continentale et la localisation de figures tectoniques majeures sur plusieurs continents (Bouchet et al., 2014 ; Blichert-Toft et al., 2016 ; Delile et al., 2014). L’existence de ces "provinces géochimiques" démontre l’intérêt des isotopes du Pb comme outil pour mieux comprendre comment l’histoire tectonique d’une région façonne la géochimie de ses continents. Un premier volet de ces travaux de thèse visait à compléter la base de données existante des compositions isotopiques du Pb dans la croûte continentale européenne, grâce à l’analyse de 104 échantillons de feldspaths potassiques issus de granites principalement originaires de Catalogne, de Corse, de Galice et de Kabylie, jusqu’ici restées en blanc sur les cartes précédemment établies. Les cartes ainsi obtenues, illustrant la répartition à travers l’Europe et le bassin méditerranéen des valeurs des "paramètres géochimiques" définis par Albarède et al. (2012), exprimant à partir des rapports isotopiques du Pb mesurés l’âge modèle de la roche et les fractionnements entre l’U, le Th et le Pb enregistrés en son sein, confirment le potentiel des isotopes du Pb comme traceurs robustes de l’héritage tectonique d’une région.Mais le cœur de cette thèse a été d’appliquer cet outil reliant chimie et histoire géodynamique que sont les isotopes du Pb à un type d’échantillon géologique pour lequel des analyses de haute précision de la compositions isotopique en Pb n’avaient jamais été entreprises jusqu’à maintenant : les pétroles bruts. Pour cela, il a fallu développer une méthode analytique novatrice permettant d’extraire le Pb de quelques millilitres de pétrole brut vers une solution aqueuse adaptée aux protocoles habituels de purification indispensables à des analyses isotopiques du Pb à haute précision par MC-ICP-MS (Fetter et al., 2019). Cette méthode a ensuite été appliquée à un total de 211 échantillons de pétrole brut issus de partout dans le monde. Des échantillons de roches mères d’hydrocarbures (schistes noirs) ont également été analysés afin de compléter les premières interprétations des résultats. Ce jeu de données unique met en évidence que le Pb contenu dans les pétroles bruts résultait du mélange d’au moins trois composantes d’âges modèles distincts : le pôle le plus radiogénique a été identifié comme associé aux roches mères des pétroles, tandis que les deux autres, d’âges modèles paléozoïque et protérozoïque, suggèrent des interactions conséquentes entre le pétrole et les roches encaissantes et sous-jacentes. Un nouveau modèle de migration du pétrole depuis sa roche mère a donc été proposé (Fetter et al., soumis), prenant en compte la forte implication des eaux circulant en profondeur dans les bassins sédimentaires en faisant intervenir un phénomène grandement négligé jusqu’à maintenant : la solubilité mutuelle de l’eau et du pétrole à haute température.La mise en évidence d’une dynamique complexe du Pb dans les pétroles bruts invalide une utilisation de ces derniers comme alternative aux feldspaths potassiques pour obtenir des données isotopiques en Pb fiables sur la croûte continentale européenne située sous les bassins sédimentaires. Cependant, elle ouvre de nouvelles portes quant à l’utilisation jusqu’ici inexplorée des isotopes du Pb comme traceurs de phénomènes de pollution associés à une prospection pétrolière peu responsable. / Lead is ubiquitous in terrestrial samples and its relationship to its radioactive ascendants, U and Th, makes it a prime tracer of geodynamic processes.The team of Janne Blichert-Toft and Francis Albarède, based in Lyon (France), has demonstrated on several continents, through large compilations of literature data supplemented by new measurements, a correspondence between the distribution of Pb isotopic compositions in the continental crust and major tectonic features (Bouchet et al., 2014 ; Blichert-Toft et al., 2016 ; Delile et al., 2014). The existence of these "geochemical provinces" has firmly established the potential of Pb isotopes as a tool for understanding how the tectonic history of a given region shaped its geochemistry. A first aspect of this PhD aimed at complementing the existing database of Pb isotopic compositions of the European continental crust through the analysis of 104 K-feldspar samples separated from granites originating mainly from Catalonia, Corsica, Galicia, and Kabylie, up until this PhD blank areas on the compiled map. The resulting updated maps showing the distribution throughout Europe and the circum-Mediterranean area of the "geochemical parameters" defined by Albarède et al. (2012), which derive a model age and fractionations between U, Th, and Pb from measured Pb isotopic ratios, confirm the potential of Pb isotopes as powerful tracers of the tectonic heritage of a given region.The core of this PhD, however, was to apply this tool connecting chemistry and geodynamic history to a type of geological sample so far never analyzed for high-precision Pb isotopic compositions: crude oil. To achieve this goal, a novel analytical method was developed which allows the extraction of Pb from a few milliliters of crude oil into an aqueous solution suitable for the standard Pb purification protocol essential for high-precision Pb isotope analysis by MC-ICPMS (Fetter et al., 2019). This method was then applied to a total of 211 crude oil samples from around the world. Hydrocarbon source rocks (black shales) also were analyzed. This unique data set reveals that Pb in crude oil results from the mixing of at least three endmembers of distinct model ages: the more radiogenic endmember is identified as the oil source rocks, while the other two components, of Paleozoic and Proterozoic ages, suggest considerable interactions between crude oil and the surrounding and underlying rocks. A new model was hence proposed for oil migration (Fetter et al., submitted), taking into account the key role of deep-seated waters circulating through the sedimentary basin by calling on a long-neglected phenomenon: mutual solubility of water and oil at high temperatures.Bringing to light the complex dynamics of Pb in crude oil invalidates the use of crude oil as an alternative to K-feldspars to obtain the Pb isotopic signature of the continental crust underlying sedimentary basins. However, it opens up new promising avenues for the yet unexplored use of Pb isotopes as tracers of irresponsible oil prospection related pollution.

Liquid chromatography (LC) coupled to mass spectrometry (MS) offers highly selective and sensitive analysis of a wide variety of compounds. However, the use of hyphenated experimental set-ups implies that many parameters may have an effect on the studied response. Therefore, in order to determine optimized experimental conditions it is of vital importance to incorporate systematic procedures during method development. In this thesis, a generic stepwise optimization strategy is proposed that aims at high chromatographic quality, as well as high mass spectrometric response. The procedure comprises (i) screening experiments to identify the most important parameters, (ii) LC studies to ensure sufficient chromatographic separation, (iii) extended infusion experiments in order to maximize precursor signal(s), and in the case of tandem MS (iv) extended infusion experiments to determine optimal conditions for collision induced dissociation and when applicable also ion trap settings. Experimental design and response surface methodology is used throughout the procedure. Further, the general applicability of LC-MS is demonstrated in this thesis. Specifically, a novel quantitative column-switched LC-MS method for ferrichrome, ferrichrysin and ferricrocin determination is presented. Using the method it was shown how the siderophore content varies with depth in podzolic soil profiles in the north and south of Sweden. The parallel approach using LC coupled to both inductively coupled plasma (ICP) mass spectrometry, and electrospray ionization (ESI) tandem MS is also evaluated as a tool to identify unknown siderophores in a sample. Additionally, different trypsin digestion schemes used for LC-ESI-MS peptide mapping were compared. By multivariate data analysis, it was clearly shown that the procedures tested induce differences that are detectable using LC-ESI-MS. Finally, the glutathione S-transferase catalyzed bioactivation of the prodrug azathioprine was verified using LC-MS.

The performance of commercial Radio Frequency Identification (RFID) tags is primarily limited by present techniques used for tag antenna design. Currently, industry techniques rely on identifying the RFID tag application (books, clothing, etc.) and then building antenna prototypes of different configurations in order to satisfy minimum read range requirements. However, these techniques inherently lack an electromagnetic basis and are unable to provide a low cost solution to the tag antenna design process. RFID tag performance characteristics (read-range, chip-antenna impedance matching, surrounding environment) can be very complex, and a thorough understanding of the RFID tag antenna design may be gained through an electromagnetic approach in order to reduce the tag antenna size and the overall cost of the RFID system. The research presented in this thesis addresses RFID tag antenna design process for passive RFID tags. With the growing number of applications (inventory, supply-chain, pharmaceuticals, etc), the proposed RFID antenna design process demonstrates procedures to design tag antennas for such applications. Electrical/geometrical properties of the antennas designed were investigated with the help of computer electromagnetic simulations in order to achieve optimal tag performance criteria such as read range, chip-impedance matching, antenna efficiency, etc. Experimental results were performed on the proposed antenna designs to compliment computer simulations and analytical modelling.

The main goal of the work presented in this thesis is to improve the reliability of existing methods for speciation analysis of organotin compounds Species-specific isotope dilution (SSID) calibration in combination with gas chromatography – inductively coupled plasma mass spectrometry was used to investigate the transformation of phenyltin species during sample preparation. Isotope-enriched phenyltin species were synthesized from corresponding isotope-enriched tin metals. SSID with a mixture of phenyltin species (PhTs) from one isotope was used to evaluate different extraction procedures for the determination of PhTs in fresh water sediment. Preparative liquid chromatography was used to produce single isotope-enriched phenyltin species making a multi-isotope spike (MI) SSID calibration possible. Different extraction procedures for the analysis of phenyltin species in biological samples were evaluated by applying MI-SSID. Degradation of TPhT and DPhT during sample extraction was observed and quantified. Accurate results were therefore obtained. A sample preparation procedure using mild extraction conditions with reasonable recoveries is described. The stability of organotin standards was investigated under different storage conditions. Mono- and diphenyltin were found to be redistributed and degraded during storage in methanol but were stabilized in sodium acetate/ acetic acid. A fast redistribution between monobutyl- and diphenyl tin has been observed and therefore it is therefore recommended that standards be derivatized as soon as possible after butyl- and phenyltin standards are mixed. Included in the thesis is also an investigation of the analytical potential of using instrumentation based on atomic absorption spectrometry (AAS) for speciation analysis of organotin compounds. The method was based on gas chromatographic separation, atomization in a quartz tube and detection by line source (LS) AAS and for comparison, by state of the art continuum source (CS) AAS. Analytical performances of CSAAS system were found to be better compared to LSAAS.

This research investigates how to draw energy from a distant emanating and alternating (i.e., AC) magnetic source and deliver it to a battery (i.e., DC). The objective is to develop, design, simulate, build, test, and evaluate a CMOS charger integrated circuit (IC) that wirelessly charges the battery of a microsystem. A fundamental challenge here is that a tiny receiver coil only produces mV's of AC voltage, which is difficult to convert into DC form. Although LC-boosted diode-bridge rectifiers in the literature today extract energy from similar AC sources, they can do so only when AC voltages are higher than what miniaturized coils can produce, unless tuned off-chip capacitors are available, which counters the aim of integration. Therefore, rather than rectify the AC voltage, this research proposes to rectify the current that the AC voltage induces in the coil. This way, the system can still draw power from voltages that fall below the inherent threshold limit of diode-bridge rectifiers. Still, output power is low because, with these low currents, small coils can only extract a diminutive fraction of the magnetic energy available, which is why investing battery energy is also part of this research. Ultimately, the significance of increasing the power that miniaturized platforms can output is higher integration and functionality of micro-devices, like wireless microsensors and biomedical implants.