Particulate and dissolved forms of arsenic and heavy metals are released from legacy mine tailings, particularly in (semi-) arid environments where tailings remain barren of vegetation and therefore highly susceptible to erosion. This leads to contamination of adjacent ecosystems and increased risk to public health. Establishment of a vegetative cap using amendments, such as composted organic matter to enhance plant growth, may be employed to reduce both physical erosion and leaching, but the impacts of such practices on molecular-scale mechanisms controlling metal(loid) speciation and lability remain poorly understood. Here we report on subsurface biogeochemical transformations of metal(loid)s in a phytostabilization field study at a Superfund site in Arizona, USA, where a legacy pyritic tailings (4,000 mg kg^-1 As, 2,438 mg kg^-1 Pb, 6,142 mg kg^-1 Zn, 13.25% Fe, and 11.71% S, averages for the top 0.5 m) has undergone oxidation in the top 1 m. Tailings were amended in the top 20 cm with 10%, 15%, and 20% composted organic matter by mass and seeded with native halotolerant plant species. All field treatments and the uncomposted control received irrigation of 0.36 ± 0.03 mm y^-1 in addition to 0.25 ± 0.16 mm y^-1 of precipitation, resulting in water input of 144% the annual precipitation rate. The field trial incorporated four annual samplings from 2010 – 2013. Sampling consisted of a single core of 90 cm in length and 2.54 cm in diameter collected from each field plot that was subsequently sectioned into 20 cm depth increments for analysis by synchrotron Fe and As X-ray absorption spectroscopy (XAS) coupled with quantitative chemical extraction methods. Subsurface stabilization of arsenic by Prosopis juliflora (mesquite) was investigated by bulk and micro synchrotron XAS and multiple-energy microscale fluorescence mapping combined with chemical digestion of plant samples following 1, 2, and 3 months of growth in greenhouse microcosms as well as 14 and 36 months of growth at the field site. Results indicate persistence of oxidizing conditions following compost amendment in surface tailings despite addition of organic matter, development of heterotrophic microbial communities and irrigation of a poorly draining medium. Compost amendment of 20% corresponded with evidence of higher oxidative pyrite weathering activity at 40-60 cm depth during phytostabilization compared to treatments of 0% or 10% compost for which the highest oxidative pyrite weathering activity was observed closer to the surface at 20-40 cm depth.. Despite observed downward transport of As, Fe, Zn, Mn, Pb, Ni, Cu, Cr, V, and Co during phytostabilization, ≥ 75% of total As was found to be attenuated by ferrihydrite in surface depths. Attenuation of Mn, Co, and Ni was observed below 40 depth by tailings receiving compost amendment relative to the irrigated control. Root associated As(V) was immobilized on the root epidermis bound to ferric sulfate precipitates and within root vacuoles as trivalent As(III)-thiol complexes. Rhizoplane associated ferric sulfate phases were dissimilar from the bulk tailings mineralogy shown by XAS and exhibited a high capacity to scavenge As(V) with As:Fe ratios 2x higher than the compost amended growth medium, indicating a root surface mechanism for their formation or accumulation. Results indicate that arsenate attenuation in semi-arid mine tailings during phytostabilization greatly depends on the presence of high concentrations of Fe(III) (oxyhydr)oxide minerals with a high capacity for arsenic adsorption.

京都大学 / 0048 / 新制・課程博士 / 博士(人間・環境学) / 甲第22859号 / 人博第967号 / 新制||人||229(附属図書館) / 2020||人博||967(吉田南総合図書館) / 京都大学大学院人間・環境学研究科相関環境学専攻 / (主査)教授 内本 喜晴, 教授 吉田 寿雄, 准教授 戸﨑 充男 / 学位規則第4条第1項該当 / Doctor of Human and Environmental Studies / Kyoto University / DFAM

El objetivo de esta tesis es estudiar la agrupación y el crecimiento de especies metálicas confinadas o soportadas en materiales porosos mediante espectroscopia de absorción de rayos X in situ. Para lograrlo, las especies de paladio y plata se han introducido en materiales porosos (¿-alúmina, carbón activo y zeolitas) mediante impregnación vía húmeda y métodos de intercambio iónico, respectivamente. Luego, el agrupamiento de estas especies metálicas se ha controlado mediante tratamientos de activación en diferentes atmósferas (inerte, oxidativa y reductiva) y seguido por XAS de manera detallada. El objetivo principal del trabajo actual es demostrar que tanto XANES como EXAFS pueden proporcionar información valiosa y, en cierto punto, innovadora durante el control de especies metálicas (en términos de tipo y tamaño de las especies). Aprovechando los procedimientos de análisis inusuales, como el análisis de los cumulantes, el ajuste de la parte imaginaria de la transformada de Fourier y otros, es posible obtener información refinada sobre los sistemas investigados. En la sección de introducción, se proporciona una compilación de estudios en los que se ha utilizado XAS como técnica importante para caracterizar especies metálicas en materiales porosos. Conscientes de que las personas pueden usar dicha introducción como base para estudios más complejos en el futuro, la discusión se ha dirigido tentativamente hacia este objetivo. El capítulo 4 se centra en el estudio de la influencia de los precursores de paladio y la naturaleza del soporte en las nanopartículas resultantes. El proceso de activación completo, es decir, la transformación precursor --> nanopartícula, ha sido seguido por XAS in situ. El análisis estuvo compuesto por el punto de partida (material impregnado), calcinación en flujo de O2 y reducción posterior con H2. La consecuencia del uso de diferentes precursores metálicos y soportes se ha discutido en términos del número de coordinación promedio obtenido a partir del análisis de datos de EXAFS, que fue respaldado por técnicas de caracterización de laboratorio. El capítulo 5 está dedicado al estudio de la agrupación de plata durante y después de los tratamientos de activación utilizando zeolitas de poro pequeño intercambiadas con plata como precursores y nanocontenedores. Se ha estudiado la influencia de la estructura y la composición química de los materiales basados en plata sobre las especies metálicas formadas en diferentes condiciones de agrupamiento y redispersión del metal (calcinación usando atmósferas distintas, reducción en H2, redispersión en O2) utilizando métodos de caracterización in situ o ex situ. Después, se discuten las consecuencias catalíticas de las zeolitas que contienen Ag en la reacción de SCO-NH3. En esta sección, la combinación de XAS in situ con varias técnicas de laboratorio ha demostrado ser fundamental para un completo entendimiento del trabajo. Finalmente, una lista de proyectos desarrollados en paralelo a esta tesis se proporciona al final de este documento. / The aim of this thesis is to study the clustering and growth of metallic species either confined or supported in porous materials by in situ X-ray absorption spectroscopy. To accomplish this task, palladium and silver species were introduced into porous materials (¿-alumina, activated carbon and zeolites) by wetness impregnation and ion-exchange methods, respectively. Then, the clustering of these metallic species was controlled by activation treatments in different atmospheres (inert, oxidative and reductive) and followed by XAS in a comprehensive way. The principal goal of current work is to demonstrate that both XANES and EXAFS can provide valuable and, at certain point, innovative information during tuning of metallic species (in terms of type and size). Taking advantage of unusual analysis procedures, such as cumulant approach, fitting of imaginary part of Fourier transform and others, it is possible to obtain refined information about the investigated systems. In the introduction section, a compilation of studies in which XAS was used as important technique to characterize metallic species in porous materials is provided. Conscious that people can use such introduction as a basis for more complex studies in the future, the discussion has been tentatively directed toward this goal. The chapter 4 is focused on the study of the influence of palladium precursors and the nature of support on the resultant nanoparticles. The whole activation process, i.e. the transformation precursor --> nanoparticle, was followed in situ by XAS. The analysis pathway was composed by the starting point (as-impregnated), calcination in O2 flow and posterior reduction with H2. The consequence of using distinct metal precursors and supports were discussed in terms of average coordination number obtained from EXAFS data analysis, which was co-supported by laboratory characterization techniques. The chapter 5 is dedicated to the study of silver clustering during and after activation treatments using Ag-containing small-pore zeolites as precursors and nanocontainers. The influence of framework structure and chemical composition of Ag-based materials on formed Ag species at different clustering and metal redispersion conditions (calcination using distinct atmospheres, reduction in H2, redispersion in O2) were studied using either in situ or ex situ characterization methods. After, the catalytic consequences of tuned Ag-containing zeolites in SCO-NH3 are discussed. In this section, the combination of in situ XAS with several laboratory techniques proved to be pivotal to have a full picture of the investigated system. Finally, a list of projects developed in parallel to this thesis is provided at the end of this document. / L'objectiu d'aquesta tesi és estudiar l'agrupació i el creixement d'espècies metàl·liques confinades o suportades en materials porosos mitjançant espectroscòpia d'absorció de raigs X in situ. Per a això, les espècies de pal·ladi i plata s'han introduït en materials porosos (¿-alúmina, carbó activat i zeolites) per mitjà de la impregnació via humida i mètodes d'intercanvi iònic, respectivament. Una vegada preparats els materials, l'agrupament de les espècies metàl·liques s'ha controlat fent ús de tractaments d'activació en diferents atmosferes (inert, oxidant i reductora) s'ha estudiat exhaustivament per XAS. L'objectiu principal del treball és demostrar que tant el XANES com l'EXAFS proporcionen informació rellevant i, en certa manera, innovadora per al control d'espècies metàl·liques (en termes de tipus i grandària d'aquestes espècies). Fent ús de procediments de tractament de dades no molt habituals com l'anàlisi de cumulants, l'ajust de la part imaginària de la transformada de Fourier i altres, és possible obtenir informació detallada sobre els sistemes estudiats. En l'apartat de la introducció, es proporciona una recopilació d'estudis en els quals s'ha utilitzat XAS com a tècnica principal per a caracteritzar les anomenades espècies metàl·liques en materials porosos. Aquesta introducció ha estat redactada per a que puga servir com a punt de partida per a futurs estudis que requereixen la utilització de XAS per a la caracterització de les espècies metàl·liques presents en els catalitzadors. El capítol 4 es centra en l'estudi de la influència dels precursors de pal·ladi i la naturalesa del suport front a les nanopartícules resultants. El procés d'activació, és a dir, la transformació precursor --> nanopartícula, ha sigut estudiat per XAS in situ. L'anàlisi per XAS va comprendre els següents passos: punt de partida (material impregnat), calcinació en flux d'O2 i reducció posterior amb H2. La utilització de diferents precursors i suports metàl·lics ha permès dur a terme una discussió, referent al nombre de coordinació mitjà obtingut a partir de l'anàlisi de dades de la zona EXAFS, que ha estat recolzat per altres tècniques de caracterització. El capítol 5 s'ha dedicat a l'estudi de l'agrupació de plata intercanviada en els catalitzadors durant i després dels tractaments d'activació. S'han utilitzat zeolites de porus xicotet, com la CHA i RHO, intercanviades amb plata. L'estudi de la influència de l'estructura zeolítica i la composició química dels materials enfront dels diferents tractaments d'activació (calcinació utilitzant diferents atmosferes, reducció en presència d'H2, re-dispersió en atmosfera d'O2) es va realitzar fent ús de mètodes de caracterització in situ o ex situ. A continuació, es discuteix la influència d'aquestes espècies metàl·liques formades, utilitzant els diferents mètodes d'activació, per a la reacció d'SCO-NH3. En aquest sentit, s'ha demostrat que la combinació de XAS in situ amb diverses tècniques habituals de laboratori és fonamental per al desenvolupament d'aquest treball. Finalment, es presenta una llista de projectes, en els quals també s'ha treballat paral·lelament, on s'ha utilitzat XAS com a tècnica de caracterització. / Wittee Lopes, C. (2018). Characterization of metallic species on porous materials by in situ XAS [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/107953

L'objectif de ce travail était d'étudier de manière approfondie l'effet de l'indium dans des catalyseurs trimétalliques de reformage catalytique à base de platine, étain et indium. Des catalyseurs ont ainsi été synthétisés selon différents protocoles de préparation et de multiples caractérisations (spectroscopies Mössbauer d'étain, XANES, EXAFS, IR-CO, MEBT, chimisportion du CO, TPR et TPD) ont été mises en oeuvre afin d'élucider l'impact de l'indium sur la nature des phases métalliques présentes au sein du catalyseur. Il a ainsi été montré que la nature des sites métalliques dépend de la méthode d'introduction de l'indium. Quand l'indium est précipité avec la source d'alumine des alliages de type PtxSn sont obtenus alors que lorsque les métaux sont imprégnés sur la surface de l'alumine des espèces subsitutionnelles Pt-Sn sont formées. Il a aussi été montré que l'augmentation de la teneur en indium entraine une augmentation de la concentration atomique d'étain dans les alliage PtxSn et un remplacement de l'étain par l'indium dans les espèces substitutionnelles. Nous avons également réussi à préparer des catalyseurs avec des quantités élevées d'alliage Pt3Sn sur la base des connaissances acquises sur l'impact de l'indium et en déposant l'étain par une réaction organométallique contrôlée de surface. D'un point de vue catalytique, les tests de reformage du n-heptane mettent en évidence l'impact positif de l'indium puisque les catalyseurs à base de Pt-Sn-In sont moins sélectifs pour les réactions parasites d'hydrogénolyse et d'hydrocraquage et plus sélectifs pour l'isomérisation que les catalyseurs à base de Pt-Sn. / This work consists of a detailed study on the effect of indium in alumina supported trimetallic PtSnIn-based naphtha reforming catalysts. These catalysts were reproduced using different preparation protocols and the indium effect was investigated using 119Sn Mössbauer spectroscopy, XANES, EXAFS spectroscopies, IR-CO, STEM, CO chemisorption, TPR and TPD. It appears that the nature of the metallic active centres depends on the method with which indium was introduced. When co-precipitating the indium precursor with the Al source, PtxSn alloys were formed, whereas when metals were impregnated on the surface, substitutional Pt-Sn alloys were observed. Increasing the In content in the frst type of catalysts leads to an increase in the Sn concentration in PtxSn alloys, whereas a gradual replacement of Sn by indium in susbstitutinal alloys is observed in the second type of catalysts. These results allowed preparing catalysts with high Pt3Sn alloy contents using the effect of indium in catalysts prepared by Sn organometallic controlled surface reactions (CSR). From a catalytic point of view, n-heptane reforming tests show that trimetallic PtSnIn-based catalysts are less selective to hydrogenolysis and hydrocracking reactions, and highly selective to isomerisation, compared to the bimetallic PtSn-based catalyst.

A busca por fontes alternativas de energia é uma tendência mundial e, neste contexto, as células a combustível alimentadas com hidrogênio obtido pela reforma de biocombustíveis constitui uma das alternativas mais promissoras. Entretanto, o desempenho das células a combustível de membrana de troca protônica (PEMFC) com ânodos baseados em Pt é drasticamente reduzido quando se utiliza hidrogênio contaminado por CO, o qual é produzido no processo de reforma. Neste trabalho, a eletrocatálise da tolerância ao CO e a estabilidade de Pt/C, PtRu/C, PtFe/C, PtMo/C e PtW/C como eletrocatlisadores anódicos de célula a combustível PEM foram investigadas através de curvas de polarização e medidas on line de espectrometria de massas (EMS), análises de voltametria cíclica, difração de raios X (DRX) e absorção de raios X (XAS). Para todos os eletrocatalisadores bimetálicos, os quais apresentaram alta tolerância ao CO, os resultado de EMS mostraram que a produção de CO2 inicia-se a menores sobrepotenciais em relação ao eletrodo de hidrogênio quando comparado a Pt/C, confirmando a ocorrência do conhecido mecanismo bifuncional. Por outro lado, os resultados de XANES indicam um aumento de vacância da banda 5d da Pt para todos os catalisadores bimetálicos, particularmente para PtFe/C, o que leva a um enfraquecimento da ligação Pt-CO e conseqüente aumento da tolerância ao CO (efeito eletrônico). Para PtMo/C e PtRu/C alimentado com H2/CO, a formação de CO2 é observada mesmo quando a célula opera em circuito aberto, confirmando alguma eliminação de CO por um processo químico, muito provavelmente uma reação de deslocamento gás-água. Uma deterioração do desempenho de célula a combustível foi observada em uma função do tempo de operação. As causas desta degradação durante a operação a longo prazo fazem parte de um processo complexo que envolve diversos mecanismos paralelos, tais como: perda ou redistribuição do eletrocatalisador, corrosão do suporte de carbono e degradação do eletrólito (Nafion®). / The search for alternative sources of energy is a global trend, and in this context, the fuel cell supplied with hydrogen obtained by biofuels reforming is one of the most promising alternative. However, the performance of proton exchange membrane fuel cells (PEMFC) with Pt-based anode is drastically lowered when using CO-contain hydrogen, as that produced by reform. In this work, the electrocatalysis of CO tolerance and the stability of Pt/C, PtRu/C, PtFe/C, PtMo/C, and PtW/C electrocatalysts at a PEM fuel cell anode has been investigated using single cell polarization and on line electrochemical mass spectrometry (EMS) measurements, and cyclic voltammetry, X-ray diffraction (XRD), and X-ray absorption near edge structure (XANES) analyses of the electrocatalysts. For all bimetallic electrocatalysts, which presented higher CO tolerance, EMS results have shown that the production of CO2 starts at lower hydrogen electrode overpotentials as compared to Pt/C, confirming the occurrence of the so-called bifunctional mechanism. On the other hand, XANES results indicate an increase in the Pt 5d-band vacancies for the bimetallic catalysts, particularly for PtFe/C, this leading to a weakening of the Pt-CO bond, helping to increase the CO tolerance (the so-called electronic effect). For PtMo/C and PtRu/C supplied with H2/CO, the formation of CO2 is observed even when the cell is at open circuit, confirming some elimination of CO by a chemical process, most probably the water gas shift reaction. A decay of the fuel cell performance was observed as a function of the operation time. The causes of degradation during long-term operation were found to be a complex process that involves several parallel mechanisms, including: electrocatalyst loss or redistribution, carbon corrosion, and electrolyte (Nafion®) degradation.

Le système des nano-colonnes auto-assemblées de GeMn, riches en Mn et entourées d'une matrice de germanium quasi pure, est un matériau prometteur pour la spintronique. Selon les paramètres de croissance, les échantillons contiennent des nano-colonnes de type cohérents sur la matrice de Ge, de type amorphe, ou/et des nano-inclusions de Ge3Mn5. Ce manuscrit présente notre étude des propriétés électroniques, magnétiques et structurales des nano-colonnes de GeMn à l'aide du rayonnement synchrotron. Les mesures de la diffusion et diffraction des rayons X en incidence rasante dans des échantillons contenant des nano-colonnes cohérentes et sans précipités de Ge3Mn5 montrent un certain désordre dans les nano-colonnes. Les cartographies de l'espace réciproque ont pu être quantitativement expliquées en considérant la déformation de la matrice de germanium due à l'inclusion des nano-colonnes dans celle-ci, ainsi que par leurs corrélations de position, sans avoir recours à d'autres phases cristallines. La spectroscopie d'absorption et le dichroïsme circulaire magnétique de rayons X ont permis de sonder spécifiquement les propriétés magnétiques des atomes de Mn dans des échantillons sans précipités de Ge3Mn5. On observe une allure des spectres XAS-XMCD des nano-colonnes très similaire à celle observée dans le cas de Ge3Mn5. Le moment magnétique local sur le manganèse possède une composante orbitale faible mais non-nulle et une amplitude totale (0.8 +/- 0.1 µB) plus faible que celle attendue pour Ge3Mn5 (~2.6 µB) ou pour des atomes de Mn substitutionnels (~3 µB). Ceci indique une origine différente de la phase des nano-colonnes. Les spectres XAS-XMCD ont été calculés pour différentes structures modèles, incluant des défauts simples ainsi de nouvelles phases cristallines, les paramètres critiques des calculs ayant été identifiés. Le meilleur accord est observé pour une nouvelle phase de type Ge2Mn. / The system of self-assembled Mn-rich GeMn nanocolumns embedded in a Mn-poor germanium matrix is a promising material for spintronics applications. Depending on the growth parameters, coherent GeMn nanocolumns, amorphous GeMn nanocolumns and/or Ge3Mn5 nanoclusters can be observed. In this manuscript, we report on the investigation on the electronic, magnetic and structural properties of the GeMn nanocolumns using synchrotron techniques. Measurements using grazing incidence x-ray scattering techniques in samples containing coherent nanocolumns, free from Ge3Mn5 precipitates, show some disorder in the nanocolumns. Reciprocal space maps are quantitatively explained by considering the scattering of the Ge matrix strained by the inclusion of the nanocolumns in the matrix and their correlations in position, without requiring the consideration of different additional phases. X-ray absorption spectroscopy and x-ray magnetic circular dichroism allow for the specific probing of the Mn magnetic properties in samples free of Ge3Mn5 clusters. The lineshapes of the XAS-XMCD spectra in the nanocolumns are found to be very similar to those in Ge3Mn5. The local magnetic moment on the Mn atom possess a small but non-zero orbital component and its total magnitude is much smaller (0.8 +/- 0.1 µB) than that in Ge3Mn5 (~2.6 µB) or than that expected for fully substitutional Mn atoms (~3 µB). This points to a different nature of the nanocolumns. The XAS-XMCD spectra have been calculated for several structural models, including simple defects and new crystalline phases, and critical parameters for the calculations have been identified. The best agreement is found for a new Ge2Mn crystalline phase.

A busca por fontes alternativas de energia é uma tendência mundial e, neste contexto, as células a combustível alimentadas com hidrogênio obtido pela reforma de biocombustíveis constitui uma das alternativas mais promissoras. Entretanto, o desempenho das células a combustível de membrana de troca protônica (PEMFC) com ânodos baseados em Pt é drasticamente reduzido quando se utiliza hidrogênio contaminado por CO, o qual é produzido no processo de reforma. Neste trabalho, a eletrocatálise da tolerância ao CO e a estabilidade de Pt/C, PtRu/C, PtFe/C, PtMo/C e PtW/C como eletrocatlisadores anódicos de célula a combustível PEM foram investigadas através de curvas de polarização e medidas on line de espectrometria de massas (EMS), análises de voltametria cíclica, difração de raios X (DRX) e absorção de raios X (XAS). Para todos os eletrocatalisadores bimetálicos, os quais apresentaram alta tolerância ao CO, os resultado de EMS mostraram que a produção de CO2 inicia-se a menores sobrepotenciais em relação ao eletrodo de hidrogênio quando comparado a Pt/C, confirmando a ocorrência do conhecido mecanismo bifuncional. Por outro lado, os resultados de XANES indicam um aumento de vacância da banda 5d da Pt para todos os catalisadores bimetálicos, particularmente para PtFe/C, o que leva a um enfraquecimento da ligação Pt-CO e conseqüente aumento da tolerância ao CO (efeito eletrônico). Para PtMo/C e PtRu/C alimentado com H2/CO, a formação de CO2 é observada mesmo quando a célula opera em circuito aberto, confirmando alguma eliminação de CO por um processo químico, muito provavelmente uma reação de deslocamento gás-água. Uma deterioração do desempenho de célula a combustível foi observada em uma função do tempo de operação. As causas desta degradação durante a operação a longo prazo fazem parte de um processo complexo que envolve diversos mecanismos paralelos, tais como: perda ou redistribuição do eletrocatalisador, corrosão do suporte de carbono e degradação do eletrólito (Nafion®). / The search for alternative sources of energy is a global trend, and in this context, the fuel cell supplied with hydrogen obtained by biofuels reforming is one of the most promising alternative. However, the performance of proton exchange membrane fuel cells (PEMFC) with Pt-based anode is drastically lowered when using CO-contain hydrogen, as that produced by reform. In this work, the electrocatalysis of CO tolerance and the stability of Pt/C, PtRu/C, PtFe/C, PtMo/C, and PtW/C electrocatalysts at a PEM fuel cell anode has been investigated using single cell polarization and on line electrochemical mass spectrometry (EMS) measurements, and cyclic voltammetry, X-ray diffraction (XRD), and X-ray absorption near edge structure (XANES) analyses of the electrocatalysts. For all bimetallic electrocatalysts, which presented higher CO tolerance, EMS results have shown that the production of CO2 starts at lower hydrogen electrode overpotentials as compared to Pt/C, confirming the occurrence of the so-called bifunctional mechanism. On the other hand, XANES results indicate an increase in the Pt 5d-band vacancies for the bimetallic catalysts, particularly for PtFe/C, this leading to a weakening of the Pt-CO bond, helping to increase the CO tolerance (the so-called electronic effect). For PtMo/C and PtRu/C supplied with H2/CO, the formation of CO2 is observed even when the cell is at open circuit, confirming some elimination of CO by a chemical process, most probably the water gas shift reaction. A decay of the fuel cell performance was observed as a function of the operation time. The causes of degradation during long-term operation were found to be a complex process that involves several parallel mechanisms, including: electrocatalyst loss or redistribution, carbon corrosion, and electrolyte (Nafion®) degradation.

Les microscopes en champ proche permettent d'obtenir la topographie d'un échantillon avec une résolution pouvant atteindre la résolution atomique. Les spectroscopies de rayons-X sont des méthodes de caractérisation qui permettent de déterminer la composition et la structure élémentaire de l'échantillon avec une précision inférieure à l'Ångström. Nous avons choisi de coupler ces deux techniques en collectant localement la luminescence visible issue de l'échantillon par la pointe-sonde d'un microscope à force de cisaillement, constituée d'une fibre optique effilée de faible ouverture. Cette technique a été utilisée pour caractériser des échantillons semiconducteurs micro- et nano-structurés afin d'en obtenir simultanément la topographie et la cartographie de luminescence locale. Afin de pouvoir étendre ce concept à d'autres types de matériaux, la faisabilité de la collecte de la fluorescence X locale a été évaluée avec la microsource. Pour cela la fluorescence X émise par un échantillon a été collectée par un capillaire cylindrique équipant un détecteur EDX. L'influence du diamètre du capillaire sur le niveau de signal a été mesurée. Une simulation numérique a été développée afin d'estimer le niveau de signal obtenu en utilisant un capillaire de 1 µm de diamètre et d'optimiser la géométrie du système. En couplant la microscopie en champ proche et l'analyse XRF, à la lumière de ces résultats, il sera possible d'atteindre 100 nm de résolution latérale en environnement synchrotron et moins de 1 µm à l'aide d'une source de laboratoire. Il serait alors possible de sélectionner un objet particulier sur une surface et d'en faire l'analyse élémentaire. / Scanning Probe Microscopes allow to obtain sample topography up to atomic resolution. X-ray spectroscopies allow elemental and structural analysis of a sample with accuracy better than 1 Å. The lateral resolution is limited by the primary beam diameter, currently a few µm². We have chosen to couple this two technics. Local sample visible luminescence is collected through a low aperture sharp optical fibre, probe of a shear force microscope. This technique was used to characterize microstructured semiconducting samples to achieve simultaneously the surface topography and luminescence mapping. The results were obtained using either synchrotron radiation or a laboratory microsource equipped with a polycapillary lens. To extend this concept to a wider variety of materials, local XRF collection by an EDX detector equipped with a cylindrical X-ray capillary was tested. A cobalt sample irradiated with the microsource was used for technique evaluation. The signal magnitude dependence with the capillary diameter was measured. Modelling and numerical calculations were developed to estimate the signal magnitude that could be detected using a 1 µm diameter capillary. The optimal system geometry was determined. Scanning Probe Microscopy combined to XRF analysis could thereby lead to simultaneous acquisition of sample topography and chemical mapping. The expected lateral resolution using synchrotron radiation is 100 nm while sub 1 µm resolution is realistic with a laboratory source. This technique would allow to point a peculiar micro- or nano-object on the surface and to perform its chemical analysis.

Made available in DSpace on 2014-12-17T15:41:47Z (GMT). No. of bitstreams: 1 WashingtonCMGpdf.pdf: 1072479 bytes, checksum: d37434aed1d2ae898ee7a9fd3701e0d7 (MD5) Previous issue date: 2009-04-29 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior / This work deals with the application of X-Ray Absorption Spectroscopy on the study of the behavior of Cu2+ ions in inverse micelles. The formation of copper nanoparticles in water-in-oil microemulsions in pseudo-ternary systems of cetyl trimethylammonium Bromide (CTAB) surfactant, butanol co-surfactant, heptane as oil phase and aqueous solutions of CuSO4.5H2O, and NaBH4. The microemulsions were prepared with a fixed percentage (60 %) of oil phase and a variable water to tensoative proportion. It was observed an increase on Cu2+ reduction by the sodium borohydride in microemulsions with 13 % of aqueous phase, independent of the reaction time. For the microemulsions in which the aqueous phase is composed only by the CuSO4 solution, it was observed that the color of the solution depends on the water to surfactant ratio. These changes in color were attributed to a competition for the hidratation water between the polar head of the tensoative and Cu2+ ions with the eventual substitution of oxygen by bromine atoms in the first coordination shell of Cu2+ ions / Neste trabalho estudou-se aplica??o da espectroscopia de absor??o de raios x no estudo do comportamento dos ?ons Cu2+ em micelas inversas. Estudou-se a forma??o de nanopart?culas de cobre em microemuls?es ?gua-em-?leo de sistemas pseudo-tern?rios tensoativo (brometo de hexadeciltrimetilam?nio, CTAB)-cotensoativo (butanol) / fase oleosa (heptano) / fase aquosa (solu??es de CuSO4.5H2O, e NaBH4). As microemuls?es foram preparadas fixando em 60% a fase ?leo (Heptano) e variando 40% de fase aquosa com tensoativo/cotensoativo na mesma propor??o, sendo que a fase aquosa do agente redutor NaBH4 foi usada em excesso de 0,4 mol.L-1 e 0,8 mol.L-1 em rela??o 0,2 mol.L-1 de fase aquosa de CuSO4.5H2O. Observou-se uma maior redu??o dos ?ons Cu2+ pelo boridreto de s?dio em microemuls?es com 13% de ?gua, independente do tempo de rea??o. Para as microemuls?es em que a fase aquosa corresponde a solu??o de CuSO4, observou-se uma depend?ncia na colora??o em fun??o da rela??o entre as concentra??es de ?gua/tensoativo. Essa mudan?a de colora??o foi atribu?da a uma competi??o pelas mol?culas de ?guas entre a cabe?a polar do tensoativo e os ?ons Cu2+ com uma eventual substitui??o do oxig?nio da primeira esfera de coordena??o por bromo

Ce projet s’inscrit dans le cadre d’une étude fondamentale sur la spéciation du technétium en milieu fortement acide. Le comportement de Tc(VII) en milieu HTFMS a été étudié en absence et en présence d’irradiation α. Dans ces deux conditions différentes, les résultats spectrophotométriques de réduction de Tc (VII) obtenus pour les mélanges HTFMS-xH₂O sont similaires. L’analyse par SAX indique la formation d’un dimère cyclique de Tc(IV) complexé aux ligands triflates et formulé Tc₂O₂(CF₃SO₃)₄(H₂O)₄. Ce composé est linéarisé en TcIV-O-TcIV quand la concentration de HTFMS augmente. Dans HTFMS à +98% (CHTFMS=11,15 M), le Tc(VII) protoné, de formule TcO₃(OH)(H₂O)₂, stabilisé en absence de rayonnements ionisants externes est réduit en Tc(V) sous irradiation α. La caractérisation structurale par la spectroscopie EXAFS sur la base des calculs DFT suggère la formation d’un complexe monomère de Tc(V) avec les ligands triflates. Les deux composés [OTc(F₃CSO₃)₂(H₂O)₂]⁺ et [OTc(F₃CSO₃)₂(OH)₂]⁻ ont été proposées. En milieu H₂SO₄ concentré (CH₂SO₄ ≥ 12 M), des expériences de radiolyse α de Tc(VII) ont été menées afin de pouvoir comparer le comportement radiolytique de Tc(VII) dans les deux milieux apparentés HTFMS et H₂SO₄. Les études XANES montrent que la réduction radiolytique de Tc(VII) contribue à la formation d’un mélange de Tc(V) et Tc(VII) dans H₂SO₄ 13 M et à Tc(V) à 18 M en H₂SO₄. L’analyse des spectres EXAFS indique la formation de complexes monomères [TcO(HSO₄)₃(H₂O)₂] et [TcO(HSO₄)₃(H₂O)(OH)]⁻ en milieu H₂SO₄ 13 M et des espèces [Tc(HSO₄)₃(SO₄)(H₂O)] et [Tc(HSO₄)₃(SO₄)(OH)]⁻. / This project is part of the fundamental study of technetium speciation in highly acidic medium. The behaviour of technetium in HTFMS was carried out in the absence then in the presence of α irradiation. Given these two different conditions, spectrophotometric results of Tc(VII) reduction are similar. XAS analysis indicates the formation of a cyclic dimer of Tc(IV) complexed to triflate ligands and formulated asTc₂O₂(CF₃SO₃)₄(H₂O)₄. This compound is linearized to TcIV-O-TcIV with the increase of HTFMS concentration. At high concentration of HTFMS +98% (11.15 M), the protonated species TcO₃(OH)(H₂O)₂ which is formed in the absence of external ionizing radiations, is reduced to the V oxidation state under α irradiation. Structural characterization by EXAFS spectroscopy and DFT calculations suggests the formation of monomer species of Tc(V)-triflate complexes where [OTc(F₃CSO₃)₂(H₂O)₂]⁺ and [OTc(F₃CSO₃)₂(OH)₂]⁻ compounds were proposed. In concentrated H₂SO₄ (CH₂SO₄ ≥ 12 M), α-radiolysis experiments of Tc(VII) were performed in order to compare the radiolytic behaviour of Tc(VII) in both comparable media HTFMS and H₂SO₄. XANES studies show that radiolytic reduction of Tc(VII) leads to the formation of Tc(V)-Tc(VII) mixture in H₂SO₄ 13 M and just Tc(V) in 18 M of H₂SO₄. The analysis of EXAFS spectra is consistent with the formation of [TcO(HSO₄)₃(H₂O)₂] and [TcO(HSO₄)₃(H2O)(OH)]⁻ monomer complexes in H₂SO₄ 13 M and [Tc(HSO₄)₃(SO₄)(H₂O)] and [Tc(HSO₄)₃(SO₄)(OH)]⁻ species at 18 M of H₂SO₄.