Worldwide demand for energy is increasing rapidly, partly driven by dramatic economic growth in developing countries. This growth has sparked concerns over the finite availability of fossil fuels and the impact of their combustion on climate change. Consequently, many recent research efforts have been devoted to the development of renewable fuels and sustainable energy systems. Interest in liquid biofuels, such as ethanol, has been particularly high because these fuels fit into the conventional infrastructure for the transportation sector. Ethanol is a renewable fuel produced through the anaerobic fermentation of sugars obtained from biomass. However, the relatively high energy demand of its production process is a major factor limiting the usefulness of ethanol as a fuel. Due to the dilute nature of the fermentation product stream and the presence of the ethanol-water azeotrope, the separation processes currently used to recover anhydrous ethanol are particularly inefficient. In fact, the ethanol separation processes account for a large fraction of the total process energy demand. In the conventional ethanol separation process, ethanol is recovered using several distillation steps combined with a dehydration process. In this dissertation, a new hybrid pervaporation-distillation system, named Membrane Dephlegmation, was proposed and investigated for use in ethanol recovery. In this process, countercurrent vapour-liquid contacting is carried out on the surface of a pervaporation membrane, leading to a combination of distillation and pervaporation effects. It was intended that this new process would lead to improved economics and energy efficiency for the entire ethanol production process. The Membrane Dephlegmation process was investigated using both numerical and experimental techniques. Multiphase Computational Fluid Dynamics (CFD) was used to study vapour-liquid contacting behaviour in narrow channels and to estimate heat and mass transfer rates. Results from the CFD studies were incorporated into a simplified design model and the Membrane Dephlegmation process was studied numerically. The results indicated that the Membrane Dephlegmation process was more efficient than simple distillation and that the ethanol-water azeotrope could be broken. Subsequently, a pilot-scale experimental system was constructed using commercially available, hydrophilic NaA zeolite membranes. Results obtained from the experimental system confirmed the accuracy of the simulations.

Lorsqu'un verre libère trop rapidement le gaz qu'il contient, la disparition des arômes véhiculés par la bulle est soudaine et irrémédiable. Ainsi, la connaissance des mécanismes physiques à l'origine de la libération du CO2 dans un verre de champagne doit permettre de mener à une forme de verre propice à un épanouissement des arômes et à une effervescence durable. La contribution des processus convectifs de brassage du vin sur la désorption du CO2 demeure assez mal connue. Pour approfondir notre compréhension de ces aspects, nous analysons les processus de libération du dioxyde de carbone au cours d'une dégustation. La démarche adoptée dans cette thèse consiste à étudier les mécanismes de transferts de masse (nucléation, diffusion, évaporation) entre les phases liquide et gazeuse. Par le biais de méthodes expérimentales (tomographie laser, PIV, thermographie IR) et numérique (code CFD), nous réalisons le suivi de l'évolution instationnaire de l'écoulement diphasique dans un verre de champagne. Nous mettons en évidence un écoulement complexe, composé de multiples instabilités hydrodynamiques. Les résultats montrent également que la libération du CO2 dépend intimement de la forme du verre et de la température de service du vin. En mettant en évidence le rôle de la forme du verre sur la libération du CO2, ces travaux ont permis d'améliorer la connaissance des paramètres qui affectent ou favorisent l'effervescence au cours d'une dégustation. Ces conclusions devront être confirmées par un panel de dégustation pour montrer que la libération des arômes est étroitement liée à la forme du verre qui reçoit le vin. / When a glass releases too quickly his dissolved gas, the loss of the aromas carried by the bubbles is sudden and irreversible. So, the knowledge of the physical mechanisms at the origin of CO2 release in a glass of champagne should lead to a glass shape conducive to aromas development and at a sustainable effervescence.The contribution of mechanisms of admixture of the wine on the CO2 desorption in a glass of champagne remains still unknown. To deepen our understanding of these aspects, we analyze the carbon dioxide release processes in tasting conditions. The approach adopted in this thesis consists in studying the mass transfer mechanisms (nucleation, diffusion, evaporation) between the liquid and gaseous phase. By experimental (laser tomography, PIV, IR thermography) and numerical ways (CFD), we follow the unsteady evolution of the two phase flow in a champagne glass. We highlight a complex flow, composed of multiple hydrodynamic instabilities. The results show also that the CO2 release strongly depends on the glass shape and on the wine temperature.By highlighting the glass shape on the carbon dioxide release, these works allowed to improve the parameters knowledge which affect or favor the effervescence process in tasting conditions. These conclusions must be confirmed by a tasting panel to show that the aromas release is closely related to the glass shape.

Submitted by Rafael Santana (rafael.silvasantana@ufpe.br) on 2017-07-12T18:01:48Z No. of bitstreams: 2 license_rdf: 811 bytes, checksum: e39d27027a6cc9cb039ad269a5db8e34 (MD5) Aida Avendano_Dissertacao_Eng Mecanica_UFPE.pdf: 2879829 bytes, checksum: 90b10e461eb8407986cea09be582a591 (MD5) / Made available in DSpace on 2017-07-12T18:01:48Z (GMT). No. of bitstreams: 2 license_rdf: 811 bytes, checksum: e39d27027a6cc9cb039ad269a5db8e34 (MD5) Aida Avendano_Dissertacao_Eng Mecanica_UFPE.pdf: 2879829 bytes, checksum: 90b10e461eb8407986cea09be582a591 (MD5) Previous issue date: 2016-01-29 / PRH-PB203 EQUIPAMENTOS/PETROBRAS / O processo de transferência de calor e massa dentro de um absorvedor tubular em espiral de Brometo de Lítio-Água (LiBr/H2O), resfriado com água em contracorrente, foi simulado usando um modelo matemático não linear. Para a simulação criou-se um programa em Matlab, usando o método numérico iterativo. Na calibração da malha física foram utilizadas condições de trabalho do absorvedor e o coeficiente de transferência de massa efetivo, Kef, obtidos da literatura. O coeficiente de transferência de calor global, U, foi calculado usando a resistência térmica global dentro do absorvedor. Para o cálculo do coeficiente de transferência de massa e de calor da interface solução-vapor se utilizaram correlações de analogia de transferência de calor e massa. As distribuições da temperatura e concentração da solução de LiBr/H2O, e a temperatura da água de resfriamento ao longo do comprimento do absorvedor foram determinadas utilizando o programa desenvolvido e os resultados obtidos apresentaram uma boa concordância quando comparados com dados reportados na literatura. Finalmente, foi analisada a influência da variação de alguns dos parâmetros, tais como temperatura e vazão de entrada da água de resfriamento, comprimento do absorvedor e material do tubo absorvedor dentro do absorvedor utilizando o programa desenvolvido. Os resultados obtidos mostraram que o programa desenvolvido permite predizer o comportamento do processo de transferência de massa e calor dentro do absorvedor em espiral de LiBr/H2O, além de representar uma ferramenta para o dimensionamento e/ou otimização deste componente. / The mass and heat transfer process in a spiral tubular absorber of the Water/Lithium Bromide (LiBr/H2O), cooled with in counter-current, was simulated using a nonlinear mathematical model. For the simulation was developed a program in Matlab, using the iterative numerical method. For the calibration of physical mesh were used absorber working condition and effective mass transfer coefficient, Kef, obtained from the literature. The global heat transfer coefficient, U, was calculated using the global thermal resistance within the absorber. For the calculation of the mass and heat transfer coefficient of the interface vapor-solution are used analogy correlations of mass and heat transfer. The temperature distribution and concentration of LiBr/H2O, and the cooling water temperature along of the length of the absorber were determined using the program developed, and the result obtained showed good agreement when compared to the data reported in the literature. Finally, the influence of the variation the some parameters were analyzed, such as inlet temperature and mass flow of cooling water, length of the absorber and material absorber tube within the absorber using the developed program. The result obtained showed that this program allowed to predict the behavior of the mass and heat transfer process in the absorber spiral of the LiBr/H2O, also represents a tool for the design and/or optimization of this component.

This dissertation focuses on the effects of heating on superhydrophobic (SHPo) surfaces. The work is divided into two main categories: heat transfer without mass transfer and heat transfer in conjunction with mass transfer. Numerical methods are used to explore the prior while experimental methods are utilized for the latter. The numerical work explores convective heat transfer in SHPo parallel plate microchannels and is separated into two stand-alone chapters that have been published archivally. The first considers surfaces with a rib/cavity structure and the second considers surfaces patterned with a square lattice of square posts. Laminar, fully developed, steady flow with constant fluid properties is considered where the tops of the ribs and posts are maintained at a constant heat flux boundary condition and the gas/liquid interfaces are assumed to be adiabatic. For both surface configurations the overall convective heat transfer is reduced. Results are presented in the form of average Nusselt number as well as apparent temperature jump length (thermal slip length). The heat transfer reduction is magnified by increasing cavity fraction, decreasing Peclet number, and decreasing channel size relative to the micro-structure spacing. Axial fluid conduction is found to be substantial at high Peclet numbers where it is classically neglected. The parameter regimes where prior analytical works found in the literature are valid are delineated. The experimental work is divided into two stand-alone chapters with one considering channel flow and the other a pool scenario. The channel work considers high aspect ratio microchannels with one heated SHPo wall. If water saturated with dissolved air is used, the air-filled cavities of SHPo surfaces act as nucleation sites for mass transfer. As the water heats it becomes supersaturated and air can effervesce onto the SHPo surface forming bubbles that align to the underlying micro-structure if the cavities are comprised of closed cells. The large bubbles increase drag in the channel and reduce heat transfer. Once the bubbles grow large enough, they are expelled from the channel and the nucleation and growth cycle begins again. The pool work considers submerged, heated SHPo surfaces such that the nucleation behavior can be explored in the absence of forced fluid flow. The surface is maintained at a constant temperature and a range of temperatures (40 - 90 °C) are explored. Similar nucleation behavior to that of the microchannels is observed, however, the bubbles are not expelled. Natural convection coefficients are computed. The surfaces with the greatest amount of nucleation show a significant reduction in convection coefficient, relative to a smooth hydrophilic surface, due to the insulating bubble layer.

A caractérisation de l’écoulement, du transfert de chaleur et de masse lors du déplacement de gouttelettes de diamètre inferieur au millimètre dans un milieu extérieur font l’objet de notre étude. La première partie présente l’état de l’art des connaissances théoriques et expérimentales des comportements aérodynamiques ainsi que les mécanismes de transfert thermiques et massiques intervenant entre une phase dispersée et une phase continue. La deuxième partie est consacrée à l’étude du phénomène d’évaporation d’une gouttelette mono-dispersée en chute libre dans l’air. Pour cela, nous avons réalisé un dispositif expérimental. Les mesures, nous permettent de prédire l’évaporation de la gouttelette en fonction des caractéristiques physico-chimiques et de l’hygrométrie du milieu extérieur. Pour la modélisation du transfert de chaleur et de masse nous avons utilisé un modèle simple qui tient en compte du couplage entre le mouvement et les phénomènes de transferts, validé dans une précédente étude au sein du laboratoire. Un bon accord est observé. La troisième partie traite de la simulation numérique de l’interaction entre les particules sphériques dans un régime laminaire. Tout d’abord, nous avons proposé et validé un modèle simple qui ne tient pas en compte des phénomènes d’interaction. Les résultats obtenus sont en concordance avec la littérature. Par la suite, nous avons étudié l’interaction entre trois particules identiques et co-alignées. Ce modèle tient compte de la nature de la particule, du nombre du Reynolds et de la distance de séparation. Nous avons validé ce travail par une comparaison avec une étude précédente que nous avons généralisé. La dernière partie est cernée sur l’étude de la dispersion des gouttelettes dans un écoulement turbulent homogène et isotrope. Pour cela, nous avons proposé un modèle Lagrangien de suivi des trajectoires. La production de la turbulence est assurée par une condition de turbulence de grille. Nous avons considéré que les caractéristiques moyennes de l’écoulement fluide sont connues. La sélection des fluctuations de vitesse turbulente est assurée par une méthode probabiliste gaussienne que nous avons développée. La fluctuation est conservée durant un certain temps lié à turbulence, elle est renouvelée au cours du calcul. Ce renouvellement est donné par le temps caractéristique de turbulence. / The characterization of flow, mass and heat transfer during moving droplets of diameter inferior to the millimetre makes the object of our study. In the first part, we present the theoretical and experimental knowledge. In the second part, we studied the evaporation of a free falling droplet in the air. In the third part, we make a simulation of the interaction between the spherical particles in laminar flow. This model takes into account the nature of the particle, the Reynolds number and the separation distance. In the last part, we study the dispersion of droplets in a homogeneous and isotropic turbulent flow.

Afin de réduire les effets nocifs des inclusions d'alumine et d'améliorer la coulabilité de l'acier en fusion, le traitement au calcium est largement utilisé pour transformer les inclusions solides en inclusions liquides. Cependant, le traitement au calcium donne des résultats très irréguliers, difficilement explicables. Même si de nombreux efforts ont été déployés pour comprendre le comportement du calcium dans l’acier liquide, il n’a pas encore été prédit avec précision. Par conséquent, le mécanisme par lequel le calcium se dissout dans la masse fondue et transforme les inclusions solides doit être compris pour optimiser les conditions de traitement tels que la vitesse d'injection, la profondeur d'injection, le diamètre du fil d'injection, le temps d'agitation, etc. Afin de comprendre le mécanisme par lequel le calcium se dissout dans l'acier liquide, des expériences en laboratoire ont été effectuées dans un petit four à induction d'une capacité de 2,5 kg de métal. L'objectif est de confronter les résultats expérimentaux avec les résultats du modèle numérique développé. La remontée des gouttelettes de calcium ou des bulles dans l’acier liquide est un problème à trois phases (gouttelettes ou bulles de calcium/acier liquide/air au sommet). Par conséquent, une plateforme de calcul scientifique interne (ICI-tech) basée sur des méthodes par éléments finis est adaptée pour permettre la modélisation de telles solutions. Les écoulements triphasiques sont validés à l’aide de références classiques issues de la littérature. Le modèle de dissolution a été mis en oeuvre dans notre logiciel et la validation du modèle de dissolution a été réalisée. Les gouttelettes et les bulles de calcium sont étudiées dans l’acier liquide et leur coefficient de transfert de masse moyen est indiqué. Afin d'étudier le changement de phase calcium liquide/gaz, un modèle de nucléation a été implémenté dans le code ICI-tech. Un test typique est effectué où la croissance d'une bulle (vapeur d'eau) dans une eau uniformément surchauffée et la croissance d'une bulle de calcium dans du calcium liquide uniformément surchauffé sont calculées. / In order to diminish the harmful effects of aluminate inclusions and improve the castability of molten steel, calcium treatment is widely used in Aluminum killed steels. However, calcium treatment gives irregular results. Even with many efforts done to understand the behavior of calcium in liquid steel, it is not yet accurately predicted. Therefore, the mechanism by which the calcium dissolves into the liquid steel and transforms the solid inclusions must be understood to optimize the process conditions such as injection speed, injection depth, injection wire diameter, stirring time, etc. In order to understand the mechanism by which the calcium dissolves into the liquid steel, laboratory scale experiments have been performed in a small induction furnace of 2.5 kg metal capacity. The calcium injections are performed at the temperature below and above the boiling point of calcium. Then, the corresponding yields (calcium recovery) are compared. Rise of calcium droplet or bubble in liquid steel is a three-phase problem (calcium droplet or calcium bubble/liquid steel/air at the top). Therefore, an in-house scientific computational platform (ICI-tech) based on finite element methods is adapted to allow the modeling of such three-phase flows, which is validated using the classical benchmark issued from the literature. The dissolution model has been implemented in our software, and their validation has been performed. Thereafter, the rise of Calcium droplets and bubbles are studied in the liquid steel, and their respective average mass transfer coefficient in the liquid steel is reported. In order to study the calcium liquid/gas phase change, the nucleation model has been implemented in the code (ICI-tech). A typical test is performed where the growth of a bubble (water vapor) in uniformly superheated water and growth of a calcium bubble in uniformly superheated Ca liquid is computed.

Der Bericht beschäftigt sich mit spontaner Grenzflächenkonvektion und -turbulenz beim Stoff- und Wärmeübergang an fluiden Phasengrenzen zwischen zwei nicht mischbaren Phasen. Solche Effekte sind von großer industrieller Bedeutung, da die erzielten Stoffübergangsraten um ein Vielfaches über den bei gewöhnlicher Diffusion auftretenden liegen. Zwei unterschiedliche Mechanismen sind der "Motor" für die Instabilitäten: Marangoni-Instabilität: Die Grenzflächenspannung ist eine Funktion der Temperatur und der Grenzflächenkonzentration des ausgetauschten Stoffes. Schwankungen der Temperatur und der Konzentration entlang der Phasengrenze führen folglich zu Grenzflächenspannungsgradienten. Grenzflächenspannungsgetriebene Instabilitäten äußern sich durch rollenförmige oder polygonale Konvektionszellen, Eruptionen oder Turbulenz an der Phasengrenze. Schwerkraftgetriebene Instabilität: Die Dichte ist ebenfalls eine Funktion der Temperatur und der Konzentration des gelösten Stoffes. Der Transport eines Stoffes über eine fluide Phasengrenze verändert die Zusammensetzung und die Dichte der angrenzenden Flüssigkeitsschichten, sodass instabile Dichteschichtungen auftreten können. Temperaturgradienten entstehen dabei durch Freisetzung von Reaktions- und/oder Lösungsenthalpie. Auftriebsbewegungen haben die Form von Thermiken (engl. plumes, thermals). Die Phänomene der Grenzflächenkonvektion werden in einer vertikalen Kapillarspaltgeometrie untersucht. Neben Stoffsystemen mit reaktivem Stoffübergang (Neutralisation von Karbonsäuren, Hydrolyse und Veresterung von Alkanoylhloriden) kamen auch solche mit reaktionsfreiem Stoffübergang (Karbonsäuren, Tensid) zur Anwendung. Die instabile Dichteschichtung, die durch den Konzentrationsgradienten infolge der Stoffdiffusion erzeugt wird, führt zu Auftriebskonvektion in Form von Thermiken. Die Anwesenheit einer exothermen Reaktion bewirkt eine Vergrößerung des Längenwachstums der Thermiken in der oberen Phase durch Aufprägung eines zusätzlich destabilisierenden Temperaturgradienten. In der unteren Phase kommt es dagegen zum Entstehen des doppeldiffusiven Fingerregimes bei Überlagerung des destabilisierenden Konzentrationsgradienten durch den stabilisierenden Temperaturgradienten. Beim Übergang eines Tensids konnten die für diese Stoffklasse charakteristischen Rollzellen, die durch Grenzflächenspannungsgradienten angetrieben werden, beobachtet werden. Diese Konvektionsstrukturen bleiben auf einen schmalen Bereich ober- und unterhalb der Phasengrenze beschränkt. Die Transportgleichungen für Impuls, Stoff und Wärme wurden in ihrer 2-dimensionalen Form in einen Rechenkode umgesetzt und der Übergang einer einzelnen Komponente simuliert. Die hydrodynamischen Bedingungen an der Phasengrenze wurden so formuliert, dass lokale Änderungen der Zusammensetzung und der Temperatur zu Grenzflächenspannungsgradienten führen und die Phasengrenze damit dem Marangonieffekt unterliegt. Die Stoffeigenschaften wurden mit Ausnahme der Dichte im Volumenkraftterm der Impulsgleichung als konstant angenommen, sodass dichtegetriebene Konvektionen simuliert werden können. Die verschiedenen Konvektionsformen werden durch die Simulation qualitativ gut wiedergegeben. Bei Marangonikonvektion kommt es zu einer Verschiebung des steilen Konzentrationsgradienten von der Phasengrenze in die Kerne der Phasen, was zum schnellen Absterben der Marangonikonvektion führt. Die Wiedergabe des Längenwachstums der Thermiken durch Simulation eines realen Stoffsystems ist zufriedenstellend. Ebenso gibt die Simulation eine realistische Abschätzung zu erwartender Stoffströme bei Anwesenheit hydrodynamischer Instabilitäten. Größere Abweichungen zwischen Simulation und Experiment sind jedoch bei der horizontalen Größenskala der Fingerstruktur festzustellen, die wahrscheinlich auf die Boussinesq-Approximation zurückzuführen sind.

The limiting current technique has widely been used to study liquid-solid mass transfer in various reactor configurations. In the present contribution several underlying physical aspects have been investigated in order to improve the design of mass transfer experiments. Experimentally, the significant influence of electrolyte composition and hydrodynamic conditions have been studied and quantified to ensure conditions of high reproducibility. In the course of single phase COMSOL simulations, different electrode configurations have been examined with emphasis on concentration fields and electric current distribution showing a large sensitivity of the experimental configuration on the absolute current values.

This dissertation presents the development of two unique measurement platforms. <br><br>The first system is a high-temperature Z-Meter. This system is designed to simultaneously measure the electrical resistivity, Seebeck coefficient, and thermal conductivity of a thermoelectric sample to accurately determine the figure of merit, ZT, for that material. It is designed to operated at sample temperatures of up to 1000C, and with temperature gradients on the order of 500C across the sample. This system also provides <i>in situ</i> load monitoring for contact pressure and allows the user to adjust loading during the experiment. <br><br>The second part of this dissertation focuses on the development of enhanced composite phase change material (PCM) heat sinks to improve passive thermal management in mobile electronics. We present a new design for a composite PCM heat sink and utilize off-the-shelf PCMs to show characterize the performance. In order to accurately investigate the performance enhancement of these designs, we develop a turn-key thermal management evaluation platform to allow the user complete control over the power profiles and cycling applied to the test chip, as well as providing <i>in situ</i> temperature monitoring within the chip. The proposed package designs show significant improvement in the length of time extended before reaching the cut-off temperature within the heatfluxes tested, 6 - 14 W/cm^2, and accomplish this while weighing less than the equivalent sensible heat storage design.<br><br><br><br>

The influence of operation parameters on the drying of spherical porous particles containing a mixture of solvents evaporating into nitrogen in a continuously worked vibrated fluid-bed dryer was studied. A simulation based on the analytical solution to heat and mass transfer equations was applied and modifications were suggested.   Four different ternary liquid mixtures were selected: Acetone-Chloroform-Methanol (ACM), Ethanol- 2-propanol-Water (EIpW), Water-Ethanol-Ethyl Acetate (WEEa) and Ethanol-Methylethylketone- Toluene (EMekT). For the solid, physical properties of Pyrex was used.   Comparison of composition- and temperature- profiles indicated that there is no resistance against heat transfer within the solid and that the heat transfer is much faster than mass transfer.   Selectivity diagrams were drawn. The results indicated that selectivity is an important parameter in predicting the drying behavior.   The retention ratio was studied as performance parameter. Its variation was studied in response to changes in operation parameters, including gas velocity and temperature, as well as solid temperature and particle size.   A  modification  to  the  model  was  examined  by  assuming  a  liquid-content-dependent  diffusion resistance factor. It was observed that implementing such an assumption yields decreased values for retention ratios.   The  effect  of  vibration  on  heat  and  mass  transfer  coefficients  was  included  using  a  correlation suggested by Sbrodov and the resulting effect on retention ratio was examined. / Inverkan   av   driftparameter  på  torkning  av   sfäriska  porösa  partiklar  som   innehåller lösningsmedelblandningar som avdunstar i kväve i en kontinuerligt viberande fluidbädd-tork studerades.  En  simuleringsmodell  baserad  på  den  analytiska  lösningen  till  värme-  och materieöverföringsekvationerna användes och ändringar föreslogs.   Fyra  olika  tärnar  vätskeblandningar  valdes:  aceton-kloroform-metanol(ACM),  etanol-2- propanolvatten,(EIpW),     vatten-etanol-etylacetat     (WEEa)     och     etanol-metyletylketon- toluen(EMekT). För den fasta fasen användes fysikaliska egenskaper liknande Pyrex.   Sammansättnings-  och  temperatur-profiler  visade  att  det  inte  finns  något  motstånd  mot värmeöverföring  i  den  fasta  fasen  och  att  värmeöverföringen  sker  mycket  snabbare  än materieöverförningen.   Selektivitetsdiagram ritades. Resultaten indikerar att selektivititen är en viktig parmeter för att förutsäga beteendet vid torkning.   Retentionsförhållandet  användes  som  ett  prestandamått.  Dess  variation  med  avseende  på förändringar av  driftsparmetrar,  bland  annat  gasen  hastighet  och  temperatur  samt  den  fasta  fasens temperatur och partikelstorlek, studerades.   En modifiering av modellen undersöktes genom att införa en vätskehalts-beroende faktor för diffusionsmotståndet. Detta minskade värdena på retentionsförhållandena.   Vibrationens inverkan på värme- och materieöverföring infördes genom att använda Sbrodov samband, och den resulterande effekten på retentionsförhållandet observerades.