Seismic hazard analyses require an estimate of earthquake ground motions from future events. These predictions are achieved through Ground Motion Prediction Equations, which include a prediction of the median and the standard deviation of ground motion parameters. The differences between observed and predicted ground motions, when normalized by the standard deviation, are referred to as epsilon (𝜖). For spectral accelerations, the correlation structure of normalized residuals across oscillator periods is important for guiding ground motion selection. Correlation structures for large global datasets have been studied extensively. These correlation structures reflect effects that are averaged over the entire dataset underlying the analyses. This paper considers the effects of site response, at given sites, on the correlation structure of normalized residuals. This is achieved by performing site response analyses for two hypothetical soil profiles using a set of 85 rock input motions. Results show that there is no significant difference between correlation coefficients for rock ground motions and correlation coefficients after considering the effects of site response for the chosen sites. / Master of Science

This master's thesis deals with the challenges of undesirable thermal expansion in lightweight materials. Thermal expansion of parts or components can lead to malfunction or breakdowns of complete systems in demanding environment where a large temperature gradient often exists. This work investigates a class of lightweight materials of which the thermal expansion coefficient can be controlled. Moreover, an additive manufacturing approach to produce these thermal management materials with high fidelity and reliability are critical to reach this goal. To achieve these two major research objectives analytic predictions, simulations, and measurement of thermal expansion coefficient with respect to temperature changes are conducted. Design and optimization of a high precision multi-material manufacturing apparatus has been conducted, leading to significant increase in production quality including reliability, efficiency, and costs. / Master of Science / This master’s thesis deals with the challenges of undesirable thermal expansion in lightweight materials. Under thermal load parts or components usually expand and this can lead to malfunction or breakdowns. To encounter this issue of the undesired expansion this work investigates a class of lightweight materials of which the thermal expansion coefficient can be controlled. Moreover, an additive manufacturing approach to produce these thermal management materials with high fidelity and reliability are critical to reach this goal. To achieve these two major research objectives analytic predictions, simulations, and measurement of thermal expansion coefficient with respect to temperature changes are conducted. Design and optimization of a high precision multi-material manufacturing apparatus has been conducted, leading to significant increase in production quality including reliability, efficiency, and costs.

The behavior of aluminum alloy ship deck panels under the thermal loads of Vertical Take-off-and Landing (VTOL) capable aircraft has become a question of interest with the introduction of new primarily aluminum alloy ships to the U.S. Naval Fleet. This study seeks to provide an initial investigation of this question by examining the transient transfer of heat through aluminum alloy ship deck panels under application of the local heat transfer similar to that of a VTOL aircraft exhaust plume core in typical operation. In this study, a jet stream intended to replicate the key physics of the core of a VTOL aircraft plume was impinged onto the upper surface of aluminum alloy corrugated deck panel test specimen. Temperature measurements are taken via thermocouples on the face of the specimen opposite the impingement to evaluate heat transfer through the specimen. This data is used to assess the effects of variation in the geometry of the corrugation between specimen. Qualitative temperature distributions were also gathered on the impingement surface via thermal imaging. A quantitative assessment of the heat paths for transverse and vertical heat transfer was made based on a thermal resistance model, leading to a conceptual description of predominant heat flow paths in the specimen, specifically weld lines between the corrugation and the flat plate surfaces. In support of this, thermal images indicated that the weld lines provided paths for heat to be pulled away from the center of heat application more rapidly than over the rest of the surface. Ultimately, heat transfer through the specimen was found to be more dependent on the flow conditions than the variations in geometry of the deck panels due to the low variation in thermal resistance across the plate. A recommendation is made based upon this observation to use the deck panels similarly to heat exchanges by adding a small amount of through-deck airflow in the areas of high heat load. / Master of Science

When a gas turbine operates in a particle laden environment, such as a desert, small solid particles are ingested into the engine. The ingested sand particles can cause damage to engine components and reduce the service life of the engine. Particle ingestion causes the erosion of metal blades and vanes, and, if the firing temperature is hot enough, deposition of molten particles in the hot sections of the engine. Both deposition and erosion phenomena can severely reduce overall engine performance. The Coefficient of Restitution (COR) is a measure of the particle-wall interaction, and has been widely used to quantify particle rebound characteristics in past particle impact studies. This work investigates the effects of temperature on sand particle impact characteristics by measuring the COR and other deposition related impact parameters. The first study presented as part of the dissertation contains a description of a novel method used to measure COR using a Particle Tracking Velocimetry (PTV) method. This is combined with Computational Fluid Dynamics (CFD) flow field to allow for an accurate determination of the particle impact velocity. The methodology described in this paper allows for measurement of the COR in a wide range of test conditions in a relatively simple manner. The COR data for two different sizes of Arizona Road Dust (ARD) and one size of glass beads are presented in this paper. Target material was stainless steel 304 and the impact angle was varied from 25 to 85 degrees. The second study details the first quantification of the COR of san particles at elevated temperatures. Temperatures used in this study were 533 K, 866 K, and 1073 K. In this study the mass flow rate through the experimental setup was fixed. This meant that velocity and temperature were coupled. Target material for this study was stainless steel 304 and the impact angle was varied from 30° to 80°. The COR was found to decrease substantially at the temperatures and velocity increased. It was determined that the decrease in COR was almost certainly caused by the increase in velocity, and not the decrease in temperature. The third study contains COR results at elevated temperatures. Significant improvements from the method used to calculate COR in the first paper are described. The particle used for these tests was an ARD sand of 20-40 μm size. Target materials used were stainless steel 304 and Hastelloy X. The particles impinged on the target coupon at a velocity of 28m/s. Tests were performed at three different temperatures, 300 K (ambient), 873 K, and 1073 K to simulate temperatures seen in gas turbine cooling flows. The angle of impingement of the bulk flow sand on the coupon was varied between 30° and 80°. A substantial decrease in COR was discovered at the elevated temperatures of this experiment. Hastelloy X exhibited a much larger decrease in COR than does stainless steel 304. The results were compared to previously published literature. The final study also used the ARD size of 20-40 μm. The target material was a nickel alloy Hastelloy X. Experiments for this study were performed at a constant velocity of 70m/s. Various temperatures ranging from 1073 K up to and including 1323 K were studied. Particle angle of impact was varied between 30° and 80°. Significant deposition was observed and quantified at the highest two temperatures. The COR of the ARD sand at the highest temperatures was found not to change despite the occurrence of deposition. At elevated temperatures, many of the particles are not molten due to sand's non-homogenous and crystalline nature. These particles rebound from the target with little if any change in COR. / Ph. D.

The dynamic of cavitation in hydraulic components cannot be computed accurately yet and therefore cavitation is hard to predict. The cavitation phenomenon can be divided in three sub-phenomenona: Pseudo-cavitation, Gas-cavitation and Vapour-cavitation. Pseudo-cavitation discribes the enlargement of an air bubble due to a pressure drop. Gas-cavitation refers to bubble growth which is driven by diffusion of dissolved air from the surrounding fluid into the bubble, when the solubility of air in the fluid is lowered by a pressure drop. Vapor-cavitation is the evaporation of the liquid phase on the bubble surface. Usually all three sub-phenomenona occur simultaneously when the pressure decreases and are summarised as cavitation in general. To implement the physics of gas-cavitation in a dynamic mathematical model it is necessary to know the diffusion coefficient of air in the hydraulic liquid and the maximum amount of air which can be dissolved in the liquid. The calculation can be accomplished by using the Bunsen coefficient. In this paper both coefficients for three different hydraulic oils are calculated based on experimental results.

Most drugs undergo passive transport during absorption and distribution in the body. It is desirable to predict passive permeation of future drug candidates in order to increase the productivity of the drug discovery process. Unlike drug-receptor interactions, there is no receptor map for passive permeability because the process of transport across the lipid bilayer involves multiple mechanisms. This work intends to increase the understanding of permeation of drug-like molecules through lipid bilayers. Drug molecules in solution typically form various species due to ionization, complexation, etc. Therefore, species specific properties must be obtained to bridge the experiment and simulations. Due to the volume contrast between intra- and extravesicular compartments of liposomes, minor perturbations in ionic and binding equilibria become significant contributors to transport rates. Using tyramine as a model amine, quantitative numerical models were developed to determine intrinsic permeability coefficients. The microscopic ionization and binding constants needed for this were independently measured. The partition coefficient in 1,9-decadiene was measured for a series of compounds as a quantitative surrogate for the partitioning into the hydrocarbon region of the bilayer. These studies uncovered an apparent long-range interaction between the two polar substituents that caused deviations in the microscopic pKa values and partition coefficient of tyramine from the expected values. Additionally the partition coefficients in the preferred binding region of the bilayer were also measured by equilibrium uptake into liposomes. All-atom molecular dynamics simulations of lipid bilayers containing tyramine, 4- ethylphenol, or phenylethylamine provided free energies of transfer of these solutes from water to various locations on the transport path. The experimentally measured partition coefficients were consistent with the free energy profiles in showing the barrier in the hydrocarbon region and preferred binding region near the interface. The substituent contributions to these free energies were also quantitatively consistent between the experiments and simulations. Specific interactions between solutes and the bilayer suggest that amphiphiles are likely to show preferred binding in the head group region and that the most of hydrogen bonds involving solutes located inside the bilayer are with water molecules. Solute re-orientation inside the bilayer lowers the partitioning barrier by allowing favorable interactions.

Ce travail s’inscrit dans le cadre de nos recherches sur les écoulements à bulles. C’est l’étude expérimentale du mélange d’un traceur très peu diffusif (fluoresceine dans l’eau) dans l’écoulement instationnaire engendré par le passage d’un écoulement uniforme au travers d’un réseau d’obstacles sphériques (2% de fraction volumique) répartis aléatoirement dans l’espace. Cet écoulement reproduit correctement les caractéristiques de l’agitation dans un essaim de bulles en ascension. La vitesse du fluide est mesurée par PIV de manière assez classique. Le traceur est injecté en amont du réseau et l’´evolution de sa concentration est mesurée par PLIF. L’utilisation de la PLIF pour mesurer des champs de grande extension (15 cm) et avec une grande dynamique d’intensité lumineuse fluorescée constitue une contribution importante de ce travail. Les résultats ainsi obtenus montrent que, à petit nombre de Reynolds, le mélange est régi par les forts gradients de vitesse qui existent dans le voisinage des sphères. A grand nombre de Reynolds, il est maîtrisé par la turbulence qui se développe alors. L’analyse des résultats comporte deux parties principales : (1) une analyse statistique des profils de concentration aboutissant à la détermination d’un coefficient de diffusion effectif et (2) une description de la distribution spectrale des fluctuations de vitesse et de concentration. / This research is a part of our research about bubbly flows. Experiments are performed about mixing of a high Schmidt scalar component (fluorescein in water) by the agitation generated by the flow through a random array of fixed spheres (at high Re and with a volume fraction of solid equal to 2%). This flow mimics for a great part the agitation in the liquid phase of a bubble swarm rising in a liquid otherwise at rest. The velocity of the liquid is estimated from PIV measurements. The scalar is injected through a point source in the array and the evolution of its concentration is estimated by PLIF method. An important part of this research is the measurement of large fields of concentration (15 cm) with a good precision by PLIF. The results show that, at moderate Reynolds number (100), mixing is controled by the steep velocity gradients located near the spheres, while, at large Reynolds number, it is controled by the turbulence that develops. The analysis of the results is composed of two parts : (1) the statistical analysis of the spatial distribution of scalar concentration, and the determination of an effective diffusion coefficient, (2) a spectral analysis of the velocity and concentration fields.

Charles University in Prague, Faculty of Pharmacy in Hradec Kralove Department of biophysics and physical chemistry Candidate: Bc. Jana Palátová Supervisor: Mgr. Monika Kuchařová, Ph.D. Title of thesis: The effect of natural cosmetics on chase the mechanical properties of the skin This thesis in theoretical part deals with the structure of skin, its biochemistry and functions. Discusses the changes that the skin undergoes during development and aging. It describes the mechanical properties of the skin and the discipline that deals with these characteristics. The practical part deals with the measurement of mechanical parameters of human skin after application of a natural cream. The trial involved a total of ten women were about the same age. Measurements were performed on a dynamic elastomers being developed at the Department of Biophysics and Physical Chemistry of the Faculty of Pharmacy at Charles University in Hradec Kralove. The investigated parameters were Hooke and Newton factor. Hooke's coefficient indicates the elasticity of the skin, Newton coefficient of its viscosity. The results show that the test cream affected as skin elasticity, and its viscosity. In 90 % of the test persons there was a significant increase in the values of the Hooke and Newton coefficient and the resulting effect...

Le coefficient de couplage électromécanique (CCEM) est un paramètre essentiel pour la description des matériaux piézoélectriques, il traduit la conversion d’énergie électrique en énergie mécanique et vice versa. Ce coefficient de couplage est étudié et déterminé dans le cadre de cette thèse pour des céramiques piézoélectriques. Ces dernières sont utilisées pour trois structures différentes ; la première structure étudiée est constituée d’une poutre longue et mince avec des petits patchs collés symétriquement sur les deux faces de la poutre en Aluminium, la seconde structure se compose d’une poutre courte et épaisse avec deux grands patchs. La dernière structure étudiée est une plaque composite multicouche du type aéronautique avec un seul grand patch. Ces trois structures ont été étudiées afin de déterminer le coefficient de couplage électromécanique effectif qui est considéré comme un indicateur de performance de l’amortissement passif shunté. Ce coefficient de couplage a été évalué de différentes manières en utilisant différents paramètres dont les conditions limites électriques, les propriétés élastiques des patchs, les propriétés modales de la poutre seule ainsi que les facteurs de couplages piézoélectriques. Une première étude expérimentale a été menée sur la poutre longue pour deux types de configurations en court circuit et circuit ouvert pour identifier ses propriétés modales. La poutre longue a été simulée pour deux types de polarisations, identiques et opposées, et simulée dans les deux codes Ansys® et Abaqus®. L’influence de la condition d’équipotentielle sur le coefficient de couplage a été étudiée. Une seconde campagne expérimentale et numérique sur une autre structure a été nécessaire pour valider les résultats obtenus. Pour pouvoir atteindre cet objectif, il était nécessaire de travailler sur une structure plus courte et plus rigide. Ainsi, la poutre courte a été simulée dans Ansys® et les résultats obtenus ont confirmé la nécessité de prendre en compte l’équipotentialité sur les faces des patchs. Cette condition a pour effet de réduire le couplage électromécanique et parfois de découpler certains modes. L’écart résultant de la corrélation expérimentale / numérique des deux poutres instrumentées a incité à recaler les modèles numériques. Ce recalage peut se présenter sous trois formes : mécanique en remplaçant l’encastrement par des ressorts linéaires, électrique en remplaçant les capacités fournies par le fabricant par les valeurs mesurées expérimentalement et électromécanique en utilisant les deux recalages précédents simultanément. Les deux poutres ont ensuite été simulées en déformations planes et contraintes planes et recalées afin d’approcher les résultats expérimentaux. L’étude de ces deux structures a permis de confronter les différentes méthodes d’évaluation du CCEM effectif, d’évaluer l’influence de l’équipotentialité sur les faces des électrodes et de comparer les simulations bidimensionnelles aux tridimensionnelles. Une plaque composite multicouche du type aéronautique a été ensuite étudiée pour généraliser la méthode d’évaluation du CCEM effectif pour les structures minces composites. La plaque seule a d’abord été simulée dans Ansys® pour valider le modèle numérique. Des tests sur la structure adaptative ont ensuite été menés pour l’évaluation du CCEM expérimental. La position choisie du patch a été déterminée par une analyse de l’énergie de déformation de la plaque seule pour les modes d’intérêt. Cette méthode de placement du patch s’est avérée efficace dans le sens où elle a conduit à des CCEM effectifs élevés pour certains modes de la bande de fréquence retenue. / The electromechanical coupling coefficient (EMCC) is an important parameter for the description of piezoelectric materials; it measures the conversion of electrical energy into mechanical one and vice versa. The coupling coefficient is studied and determined in this dissertation for piezoelectric ceramics. The latter are used for different structures: the first studied one is a long and thin Aluminium beam with small patches bonded symmetrically on its faces, the second one is a short and thick Aluminium beam with symmetrically bonded two large patches, and the third structure is considered more complex because it is an aeronautic-type multilayer composite plate with a single large patch. These three structures were studied to determine the electromechanical coupling coefficient which is considered as a performance indicator for passive shunted damping. The coupling coefficient was evaluated in different ways using different parameters, including the electrical boundary conditions, the elastic properties of the patches, the modal properties of the base beam and the piezoelectric coupling factor. A first experimental study was conducted on the long beam for two configurations, short circuit and open circuit, to identify its modal properties. The long beam was simulated for two configurations of polarization, same and opposite, in Ansys® and Abaqus® commercial codes. The equipotential condition influence on the coupling coefficient has been studied. A second experimental and numerical campaign for a different structure was necessary to validate the obtained results. For this purpose, it was necessary to work on a shorter and more stiff structure. Thus, the short beam was simulated in Ansys® which results have confirmed the necessity to consider the equipotentiality of the patches faces. This condition was found to reduce the electromechanical coupling and to uncouple some modes. The difference between experimental and numerical results of both adaptive structures was reduced by updating the numerical models. This updating is made in three ways: mechanically, by replacing the theoretical clamp conditions by linear springs, electrically, by replacing the capacities provided by the supplier by the experimental measured values, and electromechanically by considering previous updatings simultaneously. Both beams were simulated in 2D plane-strain and plane-stress and updated in order to approximate the experimental results. The study of these two structures allowed to assess different methods for the evaluation of the EMCC, to evaluate the influence of the equipotentiality constraints on the electroded faces, and to compare two-dimensional simulations to three-dimensional ones. Finally, an aeronautic-type multilayer plate composite has been studied in order to generalize the evaluation method of the EMCC for thin composite structures. The base plate was first simulated in Ansys® in order to validate the numerical model, then tests of the adaptive plate were conducted in order to evaluate the experimental EMCC. The selected position of the patch results from a strain energy analysis of the base plate for the mode of interest. The patch placement method was efficient in the sense that it provided high EMCC for some modes in the retained frequency range.

O presente trabalho investiga o fenômeno termodifusivo em dispersões coloidais de nanopartículas magnéticas de óxidos de ferro em água (ferrofluidos), com a formação de dupla camada elétrica em torno das partículas. A estabilidade da partícula em solução é controlada pela concentração de íons. Ao estabelecer uma diferença de temperatura através da amostra líquida, ocorre o efeito de termodifusão (efeito Soret) das partículas e de íons em solução. Este efeito é o movimento das partículas para o lado frio ou quente do gradiente de temperatura. O acúmulo para um dos lados do gradiente de temperatura depende das características da solução. O efeito Soret de ferrofluidos em soluções ácidas e básicas é descrito a partir da determinação experimental das grandezas físicas envolvidas na difusão das partículas. O coeficiente Soret ST e o coeficiente de difusão são determinados em experimentos ópticos de lente de matéria, utilizando o aparato experimental de Varredura-Z, e de espalhamento Rayleigh forçado para termodifusão. Para investigar a resposta dos íons ao gradiente de temperatura, são realizadas medidas do potencial termoelétrico em uma célula termoelétrica, gerado a partir da difusão das cargas dispersas no líquido. O potencial superficial das partículas também é investigado experimentalmente, para descrever a interação das partículas com o campo termoelétrico. Os experimentos são realizados em função da temperatura da amostra e usados para descrever os resultados ST(T) das partículas, a partir de equações dos principais modelos teóricos. Os resultados mostram as diferenças e semelhanças do efeito Soret das nanopartículas em soluções ácidas e básicas, e que em ambos os casos a termodifusão de nanopartículas reflete o comportamento termodifusivo dos íons dispersos em solução. / This work investigates the thermal diffusion phenomena in colloidal dispersions of iron oxide magnetic nanoparticles dispersed in water (ferrofluid). The particles are stable in water due to electrical double layer around the particles, controlled by the ionic concentration. A temperature gradient throughout the ferrofluid sample causes the thermodiffusion (Soret effect) of dispersed particles and ions. This effect is the movement of particles to the cold or hot side of the temperature gradient. The particles migration for a given side depends on the characteristics of the sample. The Soret effect of ferrofluids in acidic and basic solutions is described by the experimental measurements of the physical parameters associated to particles diffusion. The Soret coefficient ST and the mass diffusion coefficient are measured in the matter lens experiment in the Z-scan experimental setup, and by the use of Thermal Diffusion Forced Rayleigh Scattering experiments. Concerning the ionic response to the temperature gradient the thermoelectric field generated by charges diffusion is measured in a thermoelectric cell. The surface potential of the particles is also measured to describe its interactions with the thermoelectric field. These experiments are made as function of the temperature of the sample and the results are applied to describe the ST(T) of particles by the use of equations from the main theoretical models. The results show differences and resemblances of the Soret effect in acidic and basic nanoparticles solutions. In both kind of solutions the thermodiffusion of nanoparticles is mainly ruled by the thermodiffusion of ions dispersed in solution.