Les états de charmonium fournissent une source de connaissances pertinente pour déterminer les paramètres fondamentaux du Modèle Standard. Un aspect important de la compréhension et des tests de la QCD est de faire des prédictions précises du spectre des hadrons et de les tester par rapport à des données expérimentales de haute qualité. Notre cadre théorique est Lattice QCD, qui est considéré comme le seul moyen connu de traiter le lagrangien QCD complet de manière non perturbative et bien adaptée au calcul numérique. En utilisant l'action Wilson-Clover avec N_f = 2 saveurs dynamiques, nous étudierons les deux mésons charmonium eta_c et J/\psi. Nous allons également étudier certaines propriétés de leur première excitation radiale eta_c (2S) et \psi(2S). / Charmonium states provide a relevant source of knowledge for determining fundamental parameters of the Standard Model. An important aspect of understanding Quantum ChromoDynamics (QCD) is to make precise predictions of the hadron spectrum and to test them against high-quality experimental data. Our theoretical framework is Lattice QCD, which is considered to be the only known way to treat the full QCD Lagrangian non perturbatively from first principles, in a manner well suited to numerical computation. By using the Wilson-Clover action with N_f = 2 dynamical flavors, we will study the two charmonium mesons eta_c and J/\psi. We will also investigate some properties of their first radial excitations eta_c(2S) and psi(2S).

Submitted by Emanuel Varela Cardoso (emanuel.varela@ufcg.edu.br) on 2018-08-07T20:04:03Z No. of bitstreams: 1 TUILLY DE FÁTIMA MACEDO FURTADO GUERRA – DISSERTAÇÃO (PPGECA) 2016.pdf: 2570702 bytes, checksum: dc3123f0ac79b6573767e39e1c19c4c4 (MD5) / Made available in DSpace on 2018-08-07T20:04:03Z (GMT). No. of bitstreams: 1 TUILLY DE FÁTIMA MACEDO FURTADO GUERRA – DISSERTAÇÃO (PPGECA) 2016.pdf: 2570702 bytes, checksum: dc3123f0ac79b6573767e39e1c19c4c4 (MD5) Previous issue date: 2017-03-17 / Capes / O processo Anammox essencialmente é a desnitrificação autotrófica na qual nitrogênio amoniacal é oxidado por nitrito para nitrogênio molecular. O nitrito pode ser produzido em águas residuárias pela oxidação da amônia pelas Nitrosomonas. Todavia, tem-se que evitar que as bactérias do gênero Nitrobacter se desenvolvam para evitar a oxidação do nitrito para nitrato. O processo Anammox se aplica particularmente em águas ricas em amônia e pobres em material orgânico, como por exemplo, efluentes de digestores anaeróbios. Na prática tem sido aplicado com sucesso para efluentes de digestores de lodo aquecidos a 37 °C, mas a aplicação à temperatura ambiente na Europa (5 a 15 °C) não tem sido eficiente, pela dificuldade de eliminação da etapa de nitratação. Na presente pesquisa, procurou-se estabelecer se a nitrificação parcial é factível para a faixa de temperatura de esgotos no Brasil, para uma possível aplicação do processo Anammox visando à remoção de nitrogênio dos efluentes de reatores UASB. Para tanto, foram determinadas as constantes cinéticas da nitritação e nitratação em um sistema de lodo ativado entre a faixa de temperaturas de 12,7°C a 31 °C e as constantes de meia saturação do oxigênio dissolvido. A respirometria foi a ferramenta utilizada para determinar as taxas de nitritação e de nitratação e estimar as outras constantes cinéticas relevantes, sendo mostrado pelos resultados que esta é uma ferramenta útil na determinação das constantes cinéticas. Os valores encontrados das constantes cinéticas de crescimento das nitritadoras e nitratadoras em função da temperatura mostraram uma tendência de prevalecimento da nitritação sobre a nitratação em toda a faixa avaliada. Através da determinação da idade lodo mínima para a nitritação e nitratação pode-se estimar que operando um sistema de lodo ativado a temperatura ambiente adotando uma idade de lodo de 4 dias é possível promover a nitrificação parcial. / The Anammox process is essentially autotrophic denitrification in which ammoniacal nitrogen is oxidized by nitrite to molecular nitrogen. Nitrite can be produced in wastewater by the oxidation of ammonia by Nitrosomonas. However, it has to be avoided that bacteria of the genus Nitrobacter develop to avoid the oxidation of nitrite to nitrate. The Anammox process is applied particularly in ammonium rich waters and poor in organic material, such as effluent from anaerobic digesters. In practice it has been successfully applied to effluent from sludge digesters heated to 37 ° C, but application at room temperature in Europe (5 to 15 ° C) has not been efficient due to the difficulty of eliminating the nitration step. In the present research, it was tried to establish if the partial nitrification is feasible for the range of sewage temperature in Brazil, for a possible application of the Anammox process aiming at the removal of nitrogen from UASB reactor effluents. For this, the kinetic constants of nitriding and nitration were determined in an activated sludge system between the temperature range of 12.7 ° C to 31 ° C and the half-saturation constants of the dissolved oxygen. The respirometry was the tool used to determine nitration and nitration rates and to estimate the other relevant kinetic constants, and it is shown by the results that this is a useful tool in the determination of kinetic constants. The values of the kinetic constants of the nitriding and nitrating agents as a function of temperature showed a tendency of nitriding over nitration over the entire range. By determining the age minimum sludge for nitriding and nitration it can be estimated that operating a sludge activated system at room temperature adopting a sludge age of 4 days can promote partial nitrification.

Ce mémoire de thèse constitue une contribution à l'investigation des génératrices destinées à une application éolienne en mer. Le but est de rechercher les solutions optimales dans un domaine de recherche vaste contenant entre huit et onze variables d'optimisation, tout en respectant un cahier de charge bien précis. Afin d'y parvenir, un modèle multi-physique a été développé permettant la détermination des distributions du champ électromagnétique et de température dans les topologies de génératrices choisies avec prise en considération des non-linéarités des matériaux. La méthode des constantes localisées couplée aux fonctions d'interpolations a été choisie comme solution offrant un bon rapport temps de calculs/précision, prenant ainsi en considération les caractéristiques des matériaux (thermiques et magnétiques). Le modèle développé a été couplé à un algorithme d'optimisation génétique, NSGAII, permettant dans un premier temps ; d'investiguer le poids nécessaire des aimants permanents et des parties actives de deux topologies de génératrices synchrones à aimant permanent où dans la première les aimants sont montés en surfaces et dans la seconde insérés en concentration de flux, trois puissances différentes ont été investiguées 5, 8 et 15 [MW]. Dans un second temps, l'intégration d'un multiplicateur de vitesse magnétique dans la chaîne de conversion éolienne a été étudiée à travers la même approche optimale utilisée précédemment tout en comparant le poids nécessaires des aimants permanents pour ce type d'entrainement avec celle des topologies à attaque directe (sans multiplicateur de vitesse). / The aim of this PhD report is the investigation of electrical generators dedicated to an offshore wind turbine application. The main goal is to find optimal solutions in a vast research domain containing between eight and eleven optimization variables, while respecting a the imposed constraints. In order to achieve this goal, a multi-physics model was developed allowing the determination of the electromagnetic and temperature fields distributions in the selected topologies. Lumped models coupled to the interpolation functions were chosen as a solution offering a good computation time / precision ratio, thus taking into consideration the characteristics of the materials (thermal and magnetic). The developed model was coupled to a genetic optimization algorithm, NSGAII, allowing at first; the investigation of the necessary permanent magnets weight and the active parts one of two permanent magnet synchronous generator topologies where in the first the magnets are mounted in surfaces and in the second inserted in order to have flux concentration, three different powers have been investigated 5, 8 and 15 [MW]. Second, the integration of a magnetic gear in the wind energy conversion chain was studied using the same optimal approach previously used, while comparing the weight required of permanent magnets for this type of training with that of direct drive topologies (without gearbox).

Cette thèse se propose de définir les temps caractéristiques des processus d’altération à l'échelle de profil d'altération (bassin versant de Rio Icacos à Porto Rico) et de transfert sédimentaire subséquent dans les plaines alluviales (bassins du Gange et du Brahmapoutre). Cette problématique est abordée par l’analyse des nucléides des séries de désintégration radioactives de l’uranium-238. L’étude du système d’altération sphéroïdale développée sur le site de Porto Rico a permis de développer une méthode numérique de type quasi-Newton afin de résoudre le système d'équations qui rend compte du comportement des nucléides et du taux de formation de la saprolite et des couronnes d’altération.Pour les bassins du Gange et du Brahmapoutre, les sédiments ont été collectés sur différents affluents et à son exutoire. La variation des déséquilibres 238U-234U-230Th dans les sédiments, différente pour les sédiments en suspension et les sédiments à grains grossiers d’amont en aval, semble être une caractéristique générale des rivières himalayennes coulant dans la plaine Indo-gangétique. Par ce travail de thèse, nous avons montré l’utilité d’inclure l’analyse du 226Ra à l’analyse des autres nucléides de la chaîne de décroissance radioactive de l’238U (l’238U -234U-230Th 230Th) pour déterminer un taux d’altération dans un système bien défini. Néanmoins, l’étude du système du Brahmapoutre montre que la méthode proposée demande à être affinée car le transfert sédimentaire est un processus plus complexe dû à la variabilité minéralogique, granulométrique et à la dynamique sédimentaire (locale) des échantillons récoltés. / This thesis proposes to define the time-scales of weathering processes on a spheroidal weathering profile, (Rio Icacos watershed, Puerto Rico ) and the transfer time of sediments within alluvial plains (Ganges and Brahmaputra basins). This issue is addressed through the analysis of the nuclides of the 238U decay chain. The study of a spheroidal weathering system developed on the site of Puerto Rico permit to develop a limited memory quasi-Newton algorithm in order to solve the system of equations that reflects the behavior of nuclides and the rate of formation of the saprolite and the rindlet zone. For the Ganges and Brahmaputra basins, sediments were collected from different tributaries and their outlets. The variation of 238U - 234U - 230Th disequilibria in the sediments, with different variation trends for suspended and coarse-grained sediments, is probably a general feature of all Himalayan rivers flowing across the Indo-Gangetic plain. For this work, we have shown the usefulness of including the analysis of 226Ra analysis of other nuclides in the chain of radioactive decay of 238U (238U - 234U - 230Th) to determine the weathering rate in a well-defined system. Nevertheless, the study of the Brahmaputra system shows that proposed method needs to be refined as the sediment transfer is a complex process due to the mineralogical variability, size and (local) dynamics of sediments samples collected.

Dans le cadre de la conception des réacteurs, les schémas de calculs utilisant des codes de cal- culs neutroniques déterministes sont validés par rapport à un calcul stochastique de référence. Les biais résiduels sont dus aux approximations et modélisations (modèle d'autoprotection, développement en polynômes de Legendre des lois de choc) qui sont mises en oeuvre pour représenter les phénomènes physiques (absorption résonnante, anisotropie de diffusion respec- tivement). Ce document se penche sur la question de la pertinence de la modélisation de la loi de choc sur une base polynômiale tronquée. Les polynômes de Legendre sont utilisés pour représenter la section de transfert multigroupe dans les codes déterministes or ces polynômes modélisent mal la forme très piquée de ces sections, surtout dans le cadre des maillages énergétiques fins et pour les noyaux légers. Par ailleurs, cette représentation introduit aussi des valeurs négatives qui n'ont pas de sens physique. Dans ce travail, après une brève description des lois de chocs, les limites des méthodes actuelles sont démontrées. Une modélisation de la loi de choc par une fonction constante par morceaux qui pallie à ces insuffisances, a été retenue. Cette dernière nécessite une autre mod- élisation de la source de transfert, donc une modification de la méthode actuelle des ordonnées discrètes pour résoudre l'équation du transport. La méthode de volumes finis en angle a donc été développée et implantée dans l'environ- nement du solveur Sn Snatch, la plateforme Paris. Il a été vérifié que ses performances étaient similaires à la méthode collocative habituelle pour des sections représentées par des polynômes de Legendre. Par rapport à cette dernière, elle offre l'avantage de traiter les deux représenta- tions des sections de transferts multigroupes : polynômes de Legendre et fonctions constantes par morceaux. Dans le cadre des calculs des réacteurs, cette méthode mixte a été validée sur différents motifs : des cellules en réseau infini, des motifs hétérogènes et un calcul de réflecteur. Les principaux résultats sont : - un développement polynômial à l'ordre P 3 est suffisant par rapport aux biais résiduels dus aux autres modélisations (autoprotection, méthode de résolution spatiale). Cette modéli- sation est convergée au sens de l'anisotropie du choc sur les cas représentatifs des réacteurs à eau légère. - la correction de transport P 0c n'est pas adaptée, notamment sur les calculs d'absorbant B4 C. / In reactor physics, calculation schemes with deterministic codes are validated with respect to a reference Monte Carlo code. The remaining biases are attributed to the approximations and models induced by the multigroup theory (self-shielding models and expansion of the scattering law using Legendre polynomials) to represent physical phenomena (resonant absorption and scattering anisotropy respectively). This work focuses on the relevance of a polynomial expansion to model the scattering law. Since the outset of reactor physics, the latter has been expanded on a truncated Legendre polynomial basis. However, the transfer cross sections are highly anisotropic, with non-zero values for a very small range of the cosine of the scattering angle. Besides, the finer the energy mesh and the lighter the scattering nucleus, the more exacerbated is the peaked shape of this cross section. As such, the Legendre expansion is less suited to represent the scattering law. Furthermore, this model induces negative values which are non-physical. In this work, various scattering laws are briefly described and the limitations of the existing model are pointed out. Hence, piecewise-constant functions have been used to represent the multigroup scattering cross section. This representation requires a different model for the dif- fusion source. The discrete ordinates method which is widely employed to solve the transport equation has been adapted. Thus, the finite volume method for angular discretisation has been developed and imple- mented in Paris environment which hosts the Sn solver, Snatch. The angular finite volume method has been compared to the collocation method with Legendre moments to ensure its proper performance. Moreover, unlike the latter, this method is adapted for both the Legendre moments and the piecewise-constant functions representations of the scattering cross section. This hybrid-source method has been validated for different cases: fuel cell in infinite lattice, heterogeneous clusters and 1D core-reflector calculations. The main results are given below : - a P 3 expansion is sufficient to model the scattering law with respect to the biases due to the other approximations used for calculations (self-shielding, spatial resolution method). This order of expansion is converged for anisotropy representation in the modelling of light water reactors. - the transport correction, P 0c is not suited for calculations, especially for B4 C absorbant.

Made available in DSpace on 2016-06-02T20:27:40Z (GMT). No. of bitstreams: 1 TeseRJM.pdf: 817358 bytes, checksum: d24793e3f196b9f16b40acf7036bf817 (MD5) Previous issue date: 2004-12-15 / Financiadora de Estudos e Projetos / In this work we consider some nonlinear reaction-difusion equations with nonlinear Neumann boundary condition. The objective is to present conditions on the geometry of the domain, as well as on the reaction and diffusion terms, for the existence of stationary stable nonconstant solutions which develop internal and superficial transition layers. The main tools used are Gamma-convergence of functionals, variational techniques and results of dynamical systems in infinite dimension. / Neste trabalho consideramos algumas equações de reação-difusão não-lineares com condições de fronteira de Neumann não-lineares. O objetivo é apresentar condições sobre a geometria do domínio, bem como os coeficientes de reação e de difusão, para a existência de soluções estacionárias estáveis não-constantes que desenvolvem camadas de transição interna e superficial. Utilizamos como recursos principais a Gama-convergência de funcionais, técnicas variacionais e resultados de sistemas dinâmicos em dimensão infinita.

Made available in DSpace on 2016-06-02T20:27:40Z (GMT). No. of bitstreams: 1 4915.pdf: 644377 bytes, checksum: 9d13a91ba2735cf11f922800554915d1 (MD5) Previous issue date: 2013-03-07 / Universidade Federal de Sao Carlos / In this work we study two distinct problems. The first is a parabolic problem with variable diffusivity on surfaces of revolution. The objective is to find mechanisms of interaction between the diffusivity function and the geometry of the domain ensuring the existence of stationary stable nonconstant solution as well as non-existence. The second is a problem of reaction and diffusion singularly perturbed in the case of intersecting roots of the degenerate equation. We prove the existence and geometric profile of four families of stationary stable non-constant solutions to the parabolic equation. In both problems the main tools used are T-convergence theory and techniques of variational calculus. / Neste trabalho estudamos dois problemas distintos. O primeiro é um problema parabólico com difusibilidade variável sobre superfícies de revolução. O objetivo é encontrar mecanismos de interação entre a difusibilidade e a geometria do domínio que garantam a existência de soluções estacionárias estáveis não-constantes, assim como a não-existência. O segundo é um problema de reação e difusão singularmente perturbado no caso de intersecção das raízes da equação degenerada. Provamos a existência e o perfil geométrico de quatro famílias de soluções estacionárias estáveis não constantes. Para os dois problemas utilizamos como recursos principais a teoria de T- convergência e técnicas de cálculo variacional.

Made available in DSpace on 2016-06-02T20:28:24Z (GMT). No. of bitstreams: 1 2384.pdf: 452214 bytes, checksum: 195b2db7d7c702da11694b94b33fbdf1 (MD5) Previous issue date: 2009-03-24 / Universidade Federal de Sao Carlos / In this work we study a reaction-difusion problem with nonlinear Neumann boundary condition. The objective is to present suficient conditions on the diffusion coeficient so that the problem has an stable nonconstant equilibrium solution. The main tools are some basic results of real analysis, techniques of variational calculus and properties of dynamical systems. / Neste trabalho estudamos um problema de reação e difusão com condição de fronteira de Neumann não linear. O objetivo é apresentar condições suficientes sobre o coeficiente de difusão, para que o problema possua solução de equilibrio estável e não constante. Nossos principais recursos são alguns resultados básicos de análise real, técnicas do cálculo variacional e resultados referentes a sistemas dinâmicos.

L’objectif de cette thèse est d’étudier les interactions entre polyélectrolytes (PE) de charges opposées par analyse frontale continue en électrophorèse capillaire (FACCE) et par titration calorimétrique isotherme (ITC), en fonction de la force ionique du milieu et des paramètres physico-chimiques relatifs aux deux partenaires (taux de charge chimique, masse molaire, ramification). Un copolymère statistique d’acrylamide et de 2-acrylamido-2-méthyl-propane sulfonate (PAMAMPS) de taux de charge variant entre 15% et 100% a été synthétisé et caractérisé pour cette étude. En tant que polycation modèle, la poly(L-lysine) a été retenue, sous sa forme linéaire (PLL) ou ramifiée / hyperbranchée (DGL). Des mesures par turbidimétrie ont permis d’étudier la stabilité des complexes de polyélectrolytes (PEC) en fonction de la force ionique du milieu. La détermination de la stœchiométrie des PEC par 1H-RMN a permis d’établir une règle générale pour prédire les stœchiométries de charge des PEC. Les paramètres thermodynamiques d’interactions (constantes et stœchiométries d’interaction, contribution entropique et enthalpique) ont été déterminés, par le tracé systématique des isothermes d’adsorption, en considérant le modèle d’interactions des sites indépendants de même énergie. Une dépendance linéaire entre le logarithme des constantes d’interactions et le logarithme de la force ionique a été observée. Cette dépendance en force ionique confirme le caractère entropique des interactions entre PE de charges opposées. Elle permet aussi de quantifier le nombre de contre-ions relargués lors de la formation du PEC. Cette quantité de contre-ions libérés a pu être comparée à la quantité totale de contre-ions condensés. Cette modélisation permet, en outre, de prédire les constantes d’interaction pour des taux de charge intermédiaires et à différentes forces ioniques. / The aim of this thesis is to study the interactions between oppositely charged polyelectrolytes (PE) by frontal analysis continuous capillary electrophoresis (FACCE) and isothermal titration calorimetry (ITC) as a function of the ionic strength of the medium and the physico-chemical properties related to the two partners (chemical charge density, molar mass, ramification). Statistical copolymers of acrylamide and 2-acrylamido-2-methyl-propane sulfonate (PAMAMPS) with chemical charge densities varying between 15% and 100% were synthesized and characterized for this study. Poly(L-lysine) under their linear (PLL) or ramified/hyperbranched (DGL) forms were used as model polycations. Turbidity measurements allowed the study of the stability of the polyelectrolyte complexes (PEC) as a function of the ionic strength of the medium. PEC charge stoichiometries were measured by 1H-NMR, and a general predictive rule that estimates the PEC charge stoichiometry was enounced. The thermodynamic binding parameters (binding constant, stoichiometry, enthalpic and entropic contributions) were determined, by systematically plotting the isotherms of adsorption, and using the model of independent and identical interacting sites. A linear dependence between the logarithm of the binding constants and the logarithm of the ionic strength was observed. This linear dependence confirmed the entropic character of the interactions between oppositely charged PE and allowed quantifying the number of released counter-ions that were compared to the total number of condensed counter-ions. Furthermore, this modelling allowed predicting the binding constants for intermediate chemical charge densities and at different ionic strengths.

Este trabalho apresenta duas técnicas de ensaios não-destrutivos por ultra-som realizados em um tanque com água para determinar as constantes elásticas de materiais compostos de fibra de vidro/epóxi. A primeira técnica é a transmissão direta utilizando um par de transdutores. A segunda é a técnica de pulso-eco, utilizando um único transdutor. A água do tanque atua como um acoplante para transferir a energia mecânica do transdutor para a amostra. Como o transdutor não fica em contato direto com a amostra, pode-se garantir um acoplamento constante. O sistema de medição dota de um dispositivo que permite medir a velocidade da onda elástica sob diferentes ângulos de incidência, através da rotação manual da amostra. Devido ao fenômeno de conversão de modos com incidência oblíqua na interface amostra-água, ensaios por ultra-som em tanques com água fornecem as informações necessárias para o cálculo das constantes elásticas em amostras de materiais anisotrópicos, numa dada direção, a partir das medições das velocidades longitudinal e de cisalhamento. Numa dada direção de propagação em um meio anisotrópico, existem três ondas elásticas distintas: uma longitudinal e duas de cisalhamento. Se as constantes elásticas do material são conhecidas, é possível obter as três velocidades em uma dada direção bastando resolver a equação de Christoffel. Invertendo a equação de Christoffel, obtém-se as constantes elásticas a partir das velocidades medidas em uma dada direção. Os experimentos são realizados com amostras de fibra de vidro/epóxi unidirecionais e bidirecionais, utilizando transdutores com freqüências de 0,5 MHz, 1 MHz e 2,25 MHz. Os resultados experimentais obtidos utilizando ambas as técnicas são comparados com um modelo denominado “Regra das Misturas” e com resultados da literatura. / In this work, two ultrasonic non destructive techniques were implemented in a water tank and used to determine the elastic constants of glass-epoxy composites samples. The first is the through-transmission technique implemented with a pair of ultrasonic transducers. The second is the back-reflection technique that uses a single transducer in pulse-eco mode. The water acts as a couplant and transfers the mechanical energy from the transducer to the sample. As the transducer is not in direct contact with the sample, we can guarantee a good coupling with the immersion technique. With the system device, it is possible to measure the velocities of the elastic waves in different angles by manually rotating the sample. Due to wave mode conversion phenomenon at the sample-water interface with oblique incidence, ultrasonic immersion testing provides information to calculate the elastic constants of the specimen by measuring longitudinal and shear wave speeds. There are three different modes of waves, one longitudinal and two shear waves, for any given direction of propagation in an anisotropic medium. If the elastic constants of a medium are known, it is possible to obtain the three wave speeds in particular propagations directions by solving the Christoffel equation. Inverting the Christoffel equation, it is possible to obtain the elastic constants from the measured wave speed in several specific directions of the anisotropic material. Measurements were carried out on unidirectional and bidirectional glass-epoxy composite samples, using transducers with central frequency of 0.5 MHz, 1 MHz, and 2.25 MHz. The experimental results obtained with both techniques are compared with a model denominated “Rule of Mixture” estimation and with the literature.