Materiais com luminescência persistente são normalmente baseados em aluminatos e silicatos dopados com íons Eu2+, portanto buscam-se novos materiais com diferentes dopantes. Consequentemente, os materiais BaAl2O4:Eu2+,TR3+ (R: La-Lu) foram preparados pelo método de combustão com temperaturas de ignição entre 400 e 600 °C, assim como pelo método cerâmico a 1500 °C. Os sistemas mais versáteis CdSiO3:TR3+ foram preparados apenas pelo método cerâmico a 950 °C. Para estudar a estrutura e a pureza de fase dos materiais utilizou-se espectroscopia de absorção no infravermelho, difração de raios X (método do pó) e microscopia eletrônica de varredura. Os estados de oxidação e o ambiente ao redor dos íons terras raras foram investigados com a espectroscopia de absorção de raios X com radiação Síncrotron (XANES e EXAFS). As propriedades da luminescência persistente dos fósforos foram investigadas com as técnicas de termoluminescência (TL), fotoluminescência e espectroscopia com radiação Síncrotron na região do UV-UV vácuo. Baseado nas medidas de TL, a estrutura dos defeitos dos materiais BaAl2O4:Eu2+,TR3+ (TR: Nd e Dy) e CdSiO3:TR3+ (TR: Pr, Gd e Tb) mostrou-se ideal para a luminescência persistente a temperatura ambiente. Os espectros de XANES indicaram a presença dos estados divalente e trivalente do Eu dopado na matriz BaAl2O4, enquanto que apenas íons TR3+ co-dopantes foram observados (exceto CeIV). O íon Eu3+ pode estar presente devido ao processo de migração do elétron do íon Eu2+ para a banda de condução durante o processo de excitação. Em contraste, para o sistema CdSiO3:TR3+, foram observadas apenas as espécies trivalentes TR3+, excluindo, portanto, a oxidação direta TR3+→TRIV. Apenas a transição interconfiguracional 4f65d1→4f7 do íon Eu2+ foi observada na luminescência persistente dos materiais BaAl2O4:Eu2+,TR3+. Por outro lado, para a matriz CdSiO3 dopada com íons Pr3+ e Tb3+, apenas as transições 4fn-4fn foram observadas, sem a presença da banda de emissão defeitos observada tanto no espectro de emissão sob excitação no UV como no espectro de luminescência persistente do CdSiO3:Gd3+. O band gap das matrizes BaAl2O4 (6,5 eV) e CdSiO3 (5,28 eV) foi obtido com a espectroscopia de excitação no UV-UV vácuo. A posição dos níveis de energia dos íons TR2+/3+ determinada com o auxílio da banda de transferência de carga ligante metal (LMCT) O2-(2p)Eu3+ confirmou o papel dos elétrons como carregadores de carga no mecanismo da luminescência persistente dos íons Eu2+, Pr3+ e Tb3+. Por fim, os mecanismos da luminescência persistente foram desenvolvidos, e, apesar de serem diferentes, os mecanismos para os íons Eu2+, Tb3+ e Pr3+ apresentaram princípios similares. Esta semelhança confirma a solidez da interpretação dos dados experimentais dos materiais com luminescência persistentes dopados com Eu2+ e encoraja a expansão de modelos similares para outros materiais com luminescência persistente no futuro. Cálculos teóricos com, por exemplo, método DFT poderão no futuro ser utilizados para refinar o modelo, diminuir o trabalho experimental e para descobrir novos modelos para sistemas que o atual modelo não pode ser aplicado, como no caso dos materiais dopados com Eu3+. / Persistent luminescent materials are usually based on Eu2+ doped aluminates or silicates, though novel materials with different dopants are seeked for. Accordingly, BaAl2O4:Eu2+,R3+ (R: La-Lu) materials were prepared by the combustion method with ignition temperatures between 400 and 600 °C as well as with the solid state reaction at 1500 °C. The more versatile CdSiO3:R3+ systems were prepared only with the solid state reaction at 950 °C. Infrared absorption spectroscopy, X-ray powder diffraction and Scanning Electron Microscopy techniques were used to study the structure and phase purity of the materials. The oxidation states of the rare earths and their environment were investigated with synchrotron radiation X-ray absorption spectroscopy (XANES and EXAFS). The persistent luminescence properties of the phosphors were investigated with thermoluminescence (TL), photoluminescence and synchrotron radiation UV-VUV spectroscopy. Based on the TL measurements, the trap structure for BaAl2O4:Eu2+,R3+ (R: Nd and Dy) and CdSiO3:R3+ (R: Pr, Gd and Tb) is ideal for room temperature persistent luminescence. The XANES spectra indicated the presence of both divalent and trivalent europium doped in the BaAl2O4 host, while only trivalent rare earth co-dopants were observed (except CeIV). Eu3+ may be present because of in situ charging of persistent luminescence. In contrast for the CdSiO3:R3+ system, only the trivalent R3+ species were observed, thus excluding the direct R3+→RIV (R: Pr and Tb) oxidation. Only the typical interconfigurational 4f65d1→4f7 transition of Eu2+ ion was observed in the persistent luminescence of BaAl2O4:Eu2+,R3+ materials. On the other hand, for the Pr3+ and Tb3+ doped CdSiO3, only 4fn-4fn transitions were observed with no traces of the defect band emission observed in either the conventional UV excited or persistent luminescence spectra of CdSiO3:Gd3+. The band gap energy for the hosts BaAl2O4 (6.5 eV) and CdSiO3 (5.28 eV) were obtained with the UV-VUV excitation spectroscopy. The R2+/3+ energy levels positions determined with the aid of the O2-(2p)→Eu3+ ligand to metal charge transfer transition (LMCT) confirmed the role of electrons as the charge carriers in the mechanism of Eu2+, Pr3+ and Tb3+ persistent luminescence. Finally, the persistent luminescence mechanisms were constructed and, despite the differences, the mechanisms for Eu2+, Tb3+ and Pr3+ proved to be rather similar. This similarity confirms the solidity of the interpretation of experimental data for the Eu2+ doped persistent luminescence materials and encourages the expansion of similar models for other persistent luminescence materials in the future. Theoretical calculations by e.g. DFT method can be used to refine the model, to decrease experimental work and to find different models for systems where the present model evidently fails, e.g. Eu3+ doped materials.

Orientadores: Abner de Siervo e Flavio Garcia / Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Fisica Gleb Wataghin. / Made available in DSpace on 2018-08-12T11:00:44Z (GMT). No. of bitstreams: 1 Figueiredo_JoseJadsomSampaiode_M.pdf: 4194889 bytes, checksum: 489e23ac30c4fa90808ef2de00ae46d4 (MD5) Previous issue date: 2008 / Resumo: Nanopartículas (NPs) metálicas, filmes ultrafinos e sistemas nano-estruturados têm motivado vários estudos teóricos e experimentais devido a novas propriedades eletrônicas, óticas e magnéticas destes materiais. Nas NPs, tais propriedades estão diretamente relacionadas aos efeitos de tamanho (size effect) e superfície, os quais afetam suas estruturas eletrônica e cristalográfica, concentrando um maior número de átomos na superfície em relação ao seu volume. Estudos recentes têm sugerido que alguns metais nobres sem nenhum tipo de ordenamento ferromagnético espontâneo podem apresentá-lo, mesmo a temperatura ambiente, quando segmentados em forma de nanopartículas. Exemplos desses metais são Au e Pd. Apesar dos esforços para provar a existência de comportamento ferromagnético nestes materiais, não existem medidas que demonstrem de forma não ambígua a polarização ferromagnética nos átomos de Pd. Na maioria dos trabalhos mostrados na literatura, o ferromagnetismo é quantificado por magnetometria SQUID. Faz-se necessário, portanto, verificar a existência de ferromagnetismo nestes materiais utilizando-se de técnicas elemento específicas, tais como XMCD (dicroísmo circular magnético de raios X). Esta técnica é muito importante para determinação quantitativa e seletiva dos momentos magnéticos de spin e orbital para cada elemento separadamente. O nosso trabalho se diferencia em relação a estes, pois ao invés de estudarmos cada elemento individualmente trabalhamos com nanopartículas do composto bimetálico Aux Pd1-x (x =0,00, 0,25, 0,50, 0,75) passivadas por tiol. Medidas de SQUID indicaram claramente um sinal magnético nestas nanopartículas, inclusive à temperatura ambiente. Neste trabalho apresentaremos os resultados preliminares da caracterização destas nanopartículas por medidas de SQUID, XANES, XPS, bem como XMCD nas bordas L2,3 do Pd e L3 do Au . Ressaltamos também, o desenvolvimento de uma instrumentação para medidas de XMCD em ambientes de UHV onde é possível submeter às amostras a altos campos magnéticos e condições de baixas temperaturas. Com base nos resultados obtidos discutiremos a possibilidade de ferromagnetismo nestas nanopartículas e sua origem. / Abstract: Metallic Nanoparticles (NP's), ultra-thin films and nano-structured systems have motivated several theoretical and experimental works because of their new electronic optical and magnetic properties of these materials. In NP's, such properties are directly related to the size and surface effects, which affect its electronic and crystallographic structures, by concentrating a larger number of atoms on the surface in relation to their volume. Recent studies have suggested that some noble metals without any kind of spontaneous ferromagnetic order can exhibit it, even at room temperature, when segmented as nanoparticles. Examples of these metals are Au and Pd. Despite the efforts to prove the existence of a ferromagnetic behavior in such materials, there are no measurements that demonstrate unambiguously the ferromagnetic polarization in Pd atoms, for example. Most of the works shown in the literature have used SQUID measurements to characterize the ferromagnetism in these materials. It is therefore necessary to verify the existence of ferromagnetism in these materials by using element specific techniques, such as XMCD (X-ray magnetic circular dichroism). XMCD is a very important technique, which is element selective and performs quantitative determination of the spin and orbital magnetic contributions for each element separately. Our work has a particular difference when compared to others in literature because instead of studying each element individually we have worked with NP's of the bimetallic compound Aux Pd1-x (x = 0.00, 0.25, 0.50, 0.75) capped by thiol. SQUID measurements clearly showed ferromagnetic behavior in these nanoparticles, even at room temperature. In this thesis we will present results of a systematic characterization of these nanoparticles by a multi-technique approach which involves measurements with SQUID, XANES, XPS and XMCD in the L2,3 edges of the Pd and Au L3 edge. We also emphasize the development of a new instrumentation for XMCD measurements at UHV where samples can be submitted to high magnetic fields and conditions of low temperatures. Based on these findings we discuss the possibility of ferromagnetism in these nanoparticles and its origin. / Mestrado / Física da Matéria Condensada / Mestre em Física

Orientador: Silvana Moreira / Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Engenharia Civil, Arquitetura e Urbanismo / Made available in DSpace on 2018-08-21T11:33:48Z (GMT). No. of bitstreams: 1 Faria_BrunaFernandade_D.pdf: 4425637 bytes, checksum: 30ff237b5928cae8e162baf787219eb3 (MD5) Previous issue date: 2012 / Resumo: A grande geração de resíduos decorrente do acelerado crescimento populacional, da urbanização, do desenvolvimento industrial e de mudanças de hábitos de consumo da população trás como conseqüência diversos impactos ao ambiente e à saúde da população quando não gerenciados e destinados corretamente. Dentre as inúmeras formas de disposição final dos resíduos, os aterros sanitários são hoje os mais indicados às condições brasileiras, isso porque suas características construtivas permitem minimizar os impactos negativos do biogás e lixiviado produzidos. Entretanto, a garantia do confinamento dos poluentes oriundos dos aterros está ligada a sua construção e operação e quando mal construídos e/ou mal operados podem colocar em risco a qualidade do ar, da água subterrânea e águas superficiais. Diante disso, o objetivo principal deste trabalho foi analisar a concentração de metais pesados em amostras de água subterrânea, água superficial e chorume advindos de locais de disposição de resíduos sólidos da cidade de Campinas, SP - Aterro Delta, Aterro Parque Santa Bárbara e Lixão da Pirelli. As amostras foram analisadas no Laboratório Nacional de Luz Síncrotron pela técnica de Fluorescência de Raios X por Reflexão Total com Radiação Síncrotron, que se apresenta como uma metodologia multielementar e não destrutiva. A fim de quantificar o teor de metais totais as amostras de água superficial passaram por extração ácida de acordo com a metodologia EPA 200.8 e para quantificação dos metais dissolvidos as amostras foram filtradas. O mesmo ocorreu com as amostras de chorume, no entanto, para quantificação do teor dissolvido foi utilizada a metodologia de extração EPA 3050B. No Lixão da Pirelli, as maiores concentrações de metais foram encontradas em um dos poços localizados à jusante do aterro (em relação ao fluxo de água subterrâneo) - o poço de monitoramento PM04, extrapolando o valor de intervenção estipulado pela CETESB. Para o Aterro Santa Bárbara num dos poços localizados à montante do aterro, as concentrações de Ni, Mn, Pb e Cr, excederam o valor máximo permitido. No Aterro Delta as concentrações de manganês foram mais altas nos poços localizados a jusante do aterro e em relação ao chumbo, mais de 50% dos poços analisados superaram o valor máximo permitido para águas subterrâneas. Em se tratando das águas superficiais localizadas nas proximidades dos aterros estudados, os metais que extrapolaram o valor máximo permitido pela legislação na maioria dos pontos analisados foram Mn, Cu e Pb. Em relação às amostras de chorume coletadas no Aterro Delta, as concentrações médias de Mn, Ni, Cu, Zn e Pb não excederam os valores máximos permitidos. Já no Aterro Santa Bárbara as concentrações médias detectadas de Mn, Cu e Zn ultrapassaram os limites permitidos, bem como ocorrido no Aterro Pirelli para o Mn / Abstract: The great waste generation due to the accelerated population growth, urbanization and industrial developments and changes in consumer habits behind as a result many impacts to the environment and people's health if not properly managed and designed. Among the many forms of waste disposal, landfills today are best suited to Brazilian conditions, this because their construction allows minimizing the negative effects of landfill gas and slurry produced. However, the confinement of pollutants from landfills is linked to its construction and operation and when the construction and/or is wrong they can endanger air, groundwater and surface waters qualities. Thus, the main objective of this study was to analyze the concentration of heavy metals in samples of groundwater, surface water and slurry coming from solid waste disposal locations in the city of Campinas, SP - Delta, Santa Barbara and Pirelli Landfills. The samples were analyzed at the Brazilian Synchrotron Light Laboratory using Synchrotron Radiation Total Reflection X-Ray Fluorescence technique (SR-TXRF), which is a multi-element and non-destructive methodology. To quantify the total concentration of metal the surface water samples were submitted to an extraction acid procedure based on EPA 200.8 method and for the determination of dissolved contents of metals the samples were only filtered. The same procedure was applied to slurry for the determination of total concentrations, however, to quantify the dissolved contents the extraction procedure used was EPA 3050B method. In Pirelli Landfill, the highest concentrations were observed in one of the wells located to downstream of the Landfill (in relation to the groundwater flux) - the monitoring well PM04, exceeding the intervention value defined by CETESB. For Santa Barbara landfill in one upstream monitoring well the concentrations of Ni, Mn, Pb and Cr, surpassed the maximum permissive values. The manganese in Landfill Delta showed to be higher in wells located downstream and 50% of the wells analyzed exceeded the maximum permissive value for groundwater samples. In the case of surface waters located in the vicinity of landfill sites, the metals that surpassed the maximum permissive values according the legislation in most of the points analyzed were Mn, Cu and Pb. For slurry samples collected in Delta Landfill, the average concentrations for Mn, Ni, Cu and Pb not exceeded the maximum permissive values during the period studied. Moreover for Santa Barbara the average concentration of Mn, Cu and Zn surpassed the permissive limits, as was observed for Mn in the Pirelli Landfill / Doutorado / Saneamento e Ambiente / Doutora em Engenharia Civil

La microdiffraction Laue permet l'estimation des déformations élastiques à l'échelle du micron. La procédure d'analyse standard, bien établie, utilisée pour extraire les déformations élastiques des images de Laue est limitée par deux sources d'erreurs : la détermination de la positions des taches de Laue sur le détecteur, et la sensibilité aux paramètres de calibration du montage. Pour améliorer la procédure, nous avons développé une procédure appelée Laue-DIC qui utilise la très bonne résolution de la technique de corrélation d'images numériques (DIC). Cette méthode utilise, pour la détermination de l'incrément de déformation élastique et de rotation, le déplacement des pics entre deux configurations mécaniques, estimé par DIC, au lieu de leur position. Nous montrons que cette méthode donne un profil de contrainte en meilleur accord avec les solutions analytiques et numériques, pour des échantillons monocristallins déformés en flexion 4-points. Nous proposons également une méthode Laue-DIC améliorée, dans laquelle les paramètres de calibration sont estimés à chaque point de mesure, simultanément à la déformation élastique.En parallèle à la formulation de la méthode Laue-DIC (améliorée), nos efforts ont porté sur l'estimation de l'incertitude obtenue sur les déformations élastiques. Nous avons développé un modèle de bruit pour les images de Laue mesurées en rayonnement synchrotron, qui a été validé sur des séries de données, et qui nous a permis d'estimer les erreurs statistiques de la DIC, à partir d'images de Laue synthétiques. Ces erreurs ont ensuite été propagées dans la méthode Laue-DIC afin d'estimer les incertitudes sur les déformations élastiques, que l'on trouve en bon accord avec la fluctuation des contraintes locales estimées. / Laue microdiffraction is a powerful technique to characterize the intragranular elastic strain field at the scale of micrometer. Although a standard procedure extracting elastic strain and crystal orientation from Laue image has been well-established, it can suffer from two sources of uncertainties: the determination of peaks' positions and the sensitivity to calibration parameters. In light of the high accuracy of digital image correlation (DIC), we developed the so-called Laue-DIC method which used the peaks' displacements measured by DIC instead of peaks' positions to determine the elastic strain increment and rotation between two mechanical configurations. This method has been proved more efficient than the standard procedure in terms of stress profiles of bended beam. We also developed the enhanced version of Laue-DIC. By using the term “enhanced”, we mean that we attempt to obtain both lattice matrices and calibration parameters of two configurations rather than solely the elastic strain increment and rotation from peaks' displacements.Aside from the formulation of Laue-DIC, we also developed a procedure of statistically estimating the errors of elastic strain/stress resulted from DIC errors and calibration accuracy. We have first validated a classical noise model, Poissonian-Gaussian model, from diffraction images acquired at synchrotron radiation facility. With the noise model, we could statistically estimate the DIC errors by synthesizing artificial spots. The estimated DIC errors were further transmitted into the errors of Laue-DIC through statistical tests.

La connaissance du comportement mécanique à l’échelle du micron est déterminante pour arriver à prédire la dégradation des matériaux. Dans le cas des polycristaux, les lois de plasticité cristalline sont généralement utilisées pour décrire le comportement d’un grain. Ces lois possèdent de nombreux paramètres qui doivent être ajustés à l’état métallurgique et mécanique du matériau.Le travail rapporté ici explore une manière originale d’identifier ces paramètres à partir du comportement observé expérimentalement à l’échelle microscopique, sans recourir à un maillage éléments finis. Cette observation est réalisée en couplant (i) une évaluation du champ de contrainte locale par les techniques de microdiffraction Laue et d’EBSD à haute résolution angulaire et (ii) la mesure du champ de déformation total par corrélation d’images numériques.Afin de garantir la fiabilité des résultats, la justesse des mesures par microdiffraction Laue (Laue-DIC) et HR-EBSD est évaluée, pour la première fois, dans un matériau plastifié à moins de 0,5% de déformation. Les champs de déformation et de contrainte sont ensuite déterminés simultanément en surface d’une éprouvette monocristalline, sollicitée in-situ en flexion quatre points. Le comportement local est ainsi mesuré puis utilisé pour identifier deux paramètres d’une loi de plasticité cristalline, dans un acier austénitique monocristallin de type 316L. / The prediction of damage occurring in metallic materials is dependent on the knowledge of the mechanical behavior at a micron scale. Crystal plasticity laws are often used to describe the behavior of a single grain in polycrystals. Such laws include many parameters which should be tuned according to the metallurgical and mechanical state of the material.An original way to identify theses parameters is presented in this work. The local constitutive behavior is measured at the local scale. It is used to adjust the parameters’ value on a single point calculation without the need for a finite element mesh. To observe the local behavior two types of full filed measurements are carried out: (i) stress measurements using diffraction-based Laue microdiffraction and high angular resolution EBSD – HR-EBSD – and (ii) strain measurements by digital image correlation.To ensure trustworthy results, the accuracy of Laue microdiffraction (Laue-DIC) and HR-EBSD measurements are determined for the first time in a plastically deformed material. Then, stress and strain fields are monitored at the surface of a single crystal bent in-situ in the low deformation regime (0.5%). The local behavior is determined and used to identify two parameters of a crystal plasticity law, in a 316L stainless steel single crystal.

En conditions saines, le tissu osseux est constamment remodelé pour s’adapter aux différentes contraintes mécaniques, réparer les microfissures et maintenir l’homéostasie minérale. Ce remodelage est effectué par les ostéoblastes et les ostéoclastes, responsables de la formation et de la résorption du tissu osseux. Leurs activités sont orchestrées par les ostéocytes, cellules osseuses les plus abondantes, via la mechanotransduction. Dans cette thèse, nous avons utilisé la microtomographie par rayonnement synchrotron afin d’étudier la morphologie du réseau lacuno-canaliculaire (LCN), ainsi que la distribution 3D de la densité massique des tissus osseux minéralisés, sur des sujets sains ou atteints d’ostéonécrose de la mâchoire suite à un traitement par bisphosphonates (BP). Les BP sont utilisés pour le traitement de l’ostéoporose et des métastases osseuses, limitant la résorption osseuse par les ostéoclastes. Nous avons supposé que les patients ainsi traités présentaient un volume de lacunes ostéocytaires plus grand, dû à la résorption du tissu péri-lacunaire par ostéolyse ostéocytaire. Le sujet affecté par un manque de minéraux induit par la réduction du remodelage ostéoclastique, maintiendrait ainsi son homéostasie minérale. Cette hypothèse n’a pas été confirmée, mais nous avons toutefois remarqué que les lacunes larges étaient plus abondantes dans la mâchoire que dans le tibia et le fémur. Cela s’expliquerait par l’accumulation préférentielle des BP dans la mâchoire, au taux de remodelage élevé. De plus, si ces BP sont déposés dans les lacunes ostéocytaires pendant le processus de minéralisation, des concentrations toxiques pourraient être atteintes en cas d’infection, conduisant alors à une diminution du pH, et à la dissolution des minéraux. Nous avons également utilisé la nanotomographie par rayonnement synchrotron avec reconstruction de phase pour analyser la morphologie du LCN et les propriétés du tissu avoisinant, sur mâchoires de sujets sains et traités par BP. Nous supposons qu’une minéralisation secondaire a lieu via la diffusion des minéraux à travers l’interface fluide-matrice, à la surface des lacunaire et des canalicules. Cela devrait conduire à une variation de la densité massique en fonction de la distance par rapport au bord des porosités, que nous avons effectivement observé. Ainsi, l’échange minéral entre le fluide extracellulaire et la matrice minéralisée s’effectue à la frontière des lacunes et des canalicules. Nos données suggèrent que la capacité d’échange de minéraux entre le réseau poreux et la matrice osseuse augmenterait d’un ordre de grandeur si la surface canaliculaire était prise en compte. Le modèle de diffusion résultant de nos études devrait contribuer à une meilleure compréhension puis optimisation du traitement. Toutefois, des études complémentaires sur les modifications des propriétés du tissu pendant la minéralisation secondaire et les fluctuations des concentrations du minéral dans le sang sont nécessaires. / Under healthy conditions, human bone undergoes permanent remodeling to adjust to mechanical demands, to repair micro-cracks and to maintain mineral homeostasis. This process of remodeling is performed by osteoblasts and osteoclasts: bone-forming and bone-resorbing cells. The activity of osteoclasts and osteoblasts is triggered by osteocytes, the most frequently occurring type of bone cell, via mechanosensation processes. Bisphosphonates (BP) prescribed during treatment for osteoporosis or bone metastasis inhibit osteoclast activity and thus decrease the bone turnover. In this work, the distribution and morphology of osteocyte lacunae of human cortical jaw bone was investigated in 3D, and a comparison between healthy and BP-treated donors was performed using synchrotron radiation (SR) µCT. In a second approach, we used SR nano-CT with phase contrast to investigate the morphology of the canalicular network and the bone tissue properties in the vicinity of the lacuna-canalicular network of human jaw bone, originating from both healthy subjects and patients treated with BPs. We hypothesized that secondary mineralization takes place via a diffusion process through the fluid-matrix interface at both the lacunar and the canalicular surfaces. This should result in mass density gradients with respect to the distance to the pore boundary. Such mass density gradients were indeed observed at both lacunar and canalicular interfaces. We concluded that mineral exchange between extracellular fluid and mineralized matrix occurs at all bone surfaces, including the canaliculi. Our data suggested that the capacity of the pore network to exchange mineral with the bone matrix would increase by one order of magnitude if the canalicular surface is taken into account. However, more studies should be performed, targeting not only the changes of tissue properties during secondary mineralization, but also during fluctuations of mineral concentration in periods of high mineral demand.

Cette étude a été dédiée au développement d’une nouvelle approche de modélisation de la phytodisponibilité des éléments traces. Cette approche a été employée pour prédire l’adsorption du cuivre (Cu) sur des racines de blé et de tomate. Plusieurs techniques analytiques (titrages acido-basiques, résonance magnétique nucléaire, spectroscopie d’absorption X) ont été employées et croisées avec des résultats de modélisation. Dans un premier temps, la réactivité des racines a été caractérisée. Les racines étant constituées de parois apoplasmiques et de membranes plasmiques, la contribution respective de ces deux compartiments végétaux aux propriétés de complexation des racines a été évaluée. L’étude a ensuite été focalisée sur la complexation du Cu au sein des racines et sur l’évolution de cette complexation en fonction des conditions physico-chimiques du milieu. Grâce aux résultats obtenus sur la caractérisation des racines et à l’acquisition d’un jeu varié de données expérimentales sur la complexation du Cu, le modèle a pu être paramétré. Il a été montré que les propriétés de complexation des racines de blé et de tomate proviennent conjointement des membranes plasmiques et des parois apoplasmiques. La spéciation du Cu au sein des racines était partagée entre les composés pectiques des parois apoplasmiques et les protéines enchâssées à la fois dans les parois apoplasmiques et les membranes plasmiques. Un modèle propre aux racines a pu être développé sur la base d’un modèle existant dédié à la réactivité des substances humiques. Le modèle WHAM-THP, présenté dans cette étude, est un premier pas vers un nouvel outil d’évaluation de la phytodisponibilité des éléments traces. / This study has been dedicated to the development of a new modeling approach of trace element phytoavailability, focusing on binding reactions between trace element and plant roots. This approach was used to predict copper (Cu) adsorption on wheat and tomato roots. Several analytical techniques (acid-base titrations, nuclear magnetic resonance of carbon 13, X-ray absorption spectroscopy) were used and crossed with modeling results. At first, plant root reactivity was characterized. Because plant roots are consist of cell walls and plasma membranes, the relative contribution of these two compartments in root binding properties was evaluated. The study was then focused on Cu binding reactions on roots and the effects of physico-chemical conditions (pH, ionic strength, presence of cations) on copper binding. The model has been set thanks to results on root characterization obtained and the acquisition of a set of experimental data on Cu binding. It has been shown that binding properties of wheat and tomato roots came from both cell walls and plasma membranes. Copper speciation in roots was shared, almost evenly, between cell wall pectic compounds and proteins embedded in cell walls and plasma membranes. A model, specific to plant roots, has been developed on the basis of a current model dedicated to the humic substances reactivity. The WHAM-Terrestrial Higher Plants model presented in this study is a first step towards a new tool for assessing the availability of trace elements for plants.

Orientador: Silvana Moreira / Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Engenharia Civil, Arquitetura e Urbanismo / Made available in DSpace on 2018-08-22T06:30:46Z (GMT). No. of bitstreams: 1 Souza_LucianaCarlaFerreirade_D.pdf: 23739098 bytes, checksum: 19ea527d066d2fff5ef81495ee85ff0f (MD5) Previous issue date: 2013 / Resumo: O rápido crescimento urbano e industrial nas ultimas décadas provocou alterações no meio ambiente, dentre eles a poluição dos corpos d'água, principalmente por metais que podem causar danos a saúde humana. Os municípios de Campinas e Jaguariúna estão inseridos na Região Metropolitana de Campinas (RMC), uma das regiões mais dinâmicas no cenário econômico brasileiro. Portanto, visando estudar a influencia antropogenica das cidades, foi avaliada a qualidade do efluente bruto e tratado e, do lodo gerado na estação de tratamento de esgoto de Anhumas, no município de Campinas e na estação de tratamento Camanducaia no município de Jaguariúna, ambas no estado de São Paulo, principalmente no que se refere à contaminação por metais. As analises foram realizadas pela técnica de Fluorescência de Raios X por Reflexão Total com Radiação Sincrotron (SR-TXRF) e os resultados comparados com as legislações vigentes. Para o efluente tratado os dados foram comparados as legislações CONAMA 357 e 430 que estabelecem limites para o descarte de efluentes nos corpos d'água e todos os elementos Cr, Mn, Fe, Ni, Cu, Zn, Ba e Pb apresentaram concentrações em conformidade com a legislação. Para o reuso na agricultura, cujos limites são definidos pela Instrução Técnica CETESB alguns dos elementos apresentaram concentrações acima do permitido e desta forma o efluente tratado não pode ser empregado para reuso. No caso do lodo os teores de Cr, Ni, Cu, Zn, Ba e Pb foram comparados aos valores máximos permitidos das legislações CONAMA 357 e 430 e os teores de todos os elementos ficaram abaixo do valor Maximo permitido, e desta forma existe a possibilidade de aplicação do lodo no solo agrícola, para as duas estações de tratamento de esgoto estudadas, Anhumas (Campinas) e Camanducaia (Jaguariúna) / Abstract: The rapid urban and industrial growth in recent decades caused changes in the environment, including pollution of water bodies, mainly of metals that can cause harm to human health. The cities of Campinas and Jaguariuna are inserted in the Metropolitan Region of Campinas (MRC), one of the most dynamic regions in the Brazilian economy. Therefore, to study the influence of anthropogenic citiesit was evaluated the quality of raw and treated wastewater and sludge generated in the wastewater treatment plant of Anhumas, in Campinas and the treatment plant in the municipality of Camanducaia Jaguariuna, both in state of Sao Paulo, particularly with regard to metal contamination. Analyses were performed by the technique of X-ray Fluorescence by Total Reflection with Synchrotron Radiation (SR-TXRF) and the results compared with existing laws. For the treated effluent data were compared laws CONAMA 357 and 430 that set limits for the discharge of effluents into water bodies and all the elements Cr, Mn, Fe, Ni, Cu, Zn, Pb and Ba concentrations presented in accordance with legislation. To reuse in agriculture, whose limits are defined by the Technical Instruction CETESB some elements had concentrations above the permitted and thus the treated effluent can't be used for reuse. In the case of sludge contents of Cr, Ni, Cu, Zn, Ba and Pb were compared with maximum permissible values of the laws CONAMA 357 and 430 and the contents of all elements were below the maximum allowable value, and thus it is possible application of sludge to agricultural soil, for the two sewage treatment stations studied, Anhumas (Campinas) and Camanducaia (Jaguariuna) / Doutorado / Saneamento e Ambiente / Doutora em Engenharia Civil

La thèse est axée sur l'étude des effets collectifs dans un anneau de stockage d'électrons de 50 MeV, ThomX, en l'absence d'amortissement synchrotron et d’adaptation longitudinale. Cette thèse est divisée en deux parties distinctes. La première partie correspond à la conception du modèle d'impédance (champ de sillage géométrique, résistif et rayonnement synchrotron cohérent) de l'anneau de stockage afin de simuler la dynamique faisceau. Le modèle d'impédance géométrique de l'anneau de stockage a été obtenu par la simulation des éléments individuels et a été vérifié en utilisant des mesures RF sur des prototypes. Le rayonnement synchrotron cohérent a été simulé en tenant compte d'une chambre à vide rectangulaire. Des simulations de la dynamique faisceau, de la cathode de canon RF à l'anneau de stockage, comprenant les effets collectifs sont présentées. Les simulations sont utilisées pour optimiser la dynamique faisceau dans l'anneau de stockage dans le régime de micro-paquet. La deuxième partie concerne l'étude du nuage d'ions produit par l'ionisation des molécules du vide résiduel et l'optimisation des techniques de nettoyage des ions. Les points d'accumulation longitudinaux des ions et le piégeage dans les champs magnétiques sont tous les deux étudiés analytiquement et en utilisant un programme développé à cet effet. Les électrodes de nettoyage et les espaces de nettoyages sont simulés et optimisés en utilisant ce code et la stratégie choisie pour la limitation des effets induits par les ions est décrite. Enfin, les effets de la multi-ionisation et de la dissociation ionique sont pris en compte et l'effet des ions sur le faisceau d'électrons est estimé. / The thesis is focused on the study of collective effects in a 50 MeV electron storage ring, ThomX, in the absence of synchrotron radiation damping and of longitudinal matching. This thesis is divided in two distinct parts. The first part corresponds to the design of the impedance model (geometric and resistive wakefields, coherent synchrotron radiation) of the storage ring in order to simulate the beam dynamics. The geometric impedance model of the storage ring was obtained via simulation of the individual elements and was checked using wire measurements on prototypes. The coherent synchrotron radiation was simulated taking into account a rectangular vacuum chamber. Beam dynamics simulations, from the RF gun cathode to the storage ring, including collective effects are presented. The simulations are used to optimise the beam dynamics in the storage ring in the micro-bunching regime. The second part is the study of the ion cloud produced by the ionisation of the residual vacuum molecules and the optimisation of the ion clearing techniques. The longitudinal ion accumulation points and the trapping in magnetic fields are both studied analytically and by using a tracking code developed for this purpose. Clearing electrodes and clearing gaps are simulated and optimised using this code and the strategy chosen for the limitation of ion induced effects is described. Finally, the effect of multi-ionisation and ion dissociation is taken into account and the ion effect on the electron beam is estimated.

A new closed cell is presented for in situ X-ray ptychography which allows studies under gas flow and at elevated temperature. In order to gain complementary information by transmission and scanning electron microscopy, the cell makes use of a Protochips E-chipTM which contains a small, thin electron transparent window and allows heating. Two gold-based systems, 50 nm gold particles and nanoporous gold as a relevant catalyst sample, were used for studying the feasibility of the cell. Measurements showing a resolution around 40 nm have been achieved under a flow of synthetic air and during heating up to temperatures of 933 K. An elevated temperature exhibited little influence on image quality and resolution. With this study, the potential of in situ hard X-ray ptychography for investigating annealing processes of real catalyst samples is demonstrated. Furthermore, the possibility to use the same sample holder for ex situ electron microscopy before and after the in situ study underlines the unique possibilities available with this combination of electron microscopy and X-ray microscopy on the same sample.