<p>A modified liquid phase epitaxy (LPE) technique, called lateral diffusion LPE (LDLPE), is invented for low cost and high efficiency solar cell applications. Potentially, LDLPE is able to produce single crystalline silicon wafers directly from the raw material, rather than cutting wafers from single crystalline silicon ingots, therefore reducing the cost by avoiding the cutting and polishing processes.</p> <p>By using a traditional LPE method, the silicon is epitaxially grown on the silicon substrate by cooling down the saturated silicon/indium alloy solution from a high temperature. The silicon precipitates on the substrate since its solubility in the indium solvent decreases during the cooling process. A SiO₂ mask is formed on the (111) substrate with 100µm wide opening windows as seedlines. Silicon is epitaxially grown on the seedline and forms thick epitaxial lateral overgrowth (ELO) layers on the oxide mask. The ELO layers are silicon strips with an aspect ratio of 1:1 (width: thickness), approximately. The strip grows both laterally in width and vertically in thickness.</p> <p>The concept of LDLPE is to intentionally block the silicon diffusion path from the top of the seedline, but leave the lateral diffusion path from the bulk indium melt to the seedline. Theoretically, by using the LDLPE method, the silicon strip should have a larger aspect ratio, because the laterally growth in width is allowed but the vertical growth in thickness is limited. In addition, single crystalline silicon wafers can be achieved if the strip grows continuously.</p> <p>A graphite slide boat is designed to place a plate over the seedline to block the diffusion path of silicon atoms from the top of the seedline. After one growth cycle, silicon strips grown by LDLPE are wider than LPE strips but have similar thicknesses. The aspect ratios are increased from 1:1 to a number larger than 2:1. A Monte-Carlo random walk model is used to simulate the change of LDLPE strip aspect ratio caused by placing a plate over the seedline.</p> <p>Wetting seedline by indium melt is very critical for a successful growth. Due to the small space between the plate and seedline and the surface tension of the indium melt, the indium melt cannot flow into the small space. A pre-wetting technique is used to fill the space prior to loading the graphite boat into the tube furnace and solve the wetting problem successfully.</p> <p>The structure of a LDLPE silicon strip is characterized by X-ray diffraction. The electrical properties are characterized by Hall Effect measurement and photoconductive decay measurement. LDLPE silicon strips are (111) orientated single crystal and are the same orientation as the substrate. For the growth temperature of 950°C, the LDLPE strip has an estimated effective minority carrier lifetime of 30.9µs. The experimental results demonstrate that LDLPE is feasible for photovoltaic application if continuous growth and scaling up can be achieved.</p> / Doctor of Philosophy (PhD)

Multiphase systems provide an opportunity to develop both novel processing methods and create advanced materials through combining the properties of dissimilar phases in a synergistic manner. In this work, we detail the halogenation of poly(ether ether ketone) (PEEK) through both solution-state and gel-state functionalization methods. The multiphase gel-state chemistry restricts functionalization to the amorphous regions of the semi-crystalline parent homopolymer and generates a copolymer with a blocky microstructure. Solution-state functionalization yields random copolymers which provide matched sets to the blocky analogs for fundamental investigations into the effects of polymer microstructure on material properties. Halogenating PEEK using N-halosuccinimides allows for direct installation of pendant halogens along the polymer backbone with facile control of halogen identity. For both bromination and iodination, blocky halogenation of PEEK provides faster crystallization kinetics, higher glass transition (Tg) and melting temperatures as well as superior crystallizability than random halogenation. When comparing halogen identity, increasing halogen size results in increased Tgs, decreased backbone planarity, and for copolymers with blocky microstructures, an earlier onset of phase separation. Increasing halogen size also results in decreased crystallizability and crystallization kinetics, however, these deleterious effects are mitigated in blocky microstructures due to colocalization of the pristine repeat units. Iodination also results in greater flame resistance than bromination for PEEK-based copolymers, and preserved crystallizability allows for the generation of flame retardant aerogels. Direct halogenation of PEEK in the gel-state also provided a reactive microstructural template for subsequent functionalization. Through the use of copper mediated cross-coupling chemistries, the aryl halide functionalities were leveraged to decorate the polymer backbone with pendant perfluoroalkyl chains. The blocky perfluoro alkyl PEEK demonstrated preserved crystallizability and serves as a candidate for compatibilization of poly(tetrafluoroethylene)-PEEK polymer blends. Superacid-modified PEEK was synthesized through a similar methodology and demonstrated over 50,000% increased hygroscopicity relative to the parent homopolymer, and exhibited preserved crystallizability. Multiphase systems were also designed to additively manufacture reinforced elastomers through vat photopolymerization using a degradable scaffold approach that challenged the current paradigm that the scaffold only serves as a geometrical template in vat photopolymerization. The scaffold crosslinks were cleaved through a reactive extraction process that liberated the glassy photopolymer backbone and resulted in over 200% increased ultimate strain and 50% increased ultimate stress relative to a control that was subjected to a neutral extraction. Lastly, thermoresponsive micellar ligands were synthesized as a multiphase approach to environmental remediation of metal-contaminated aqueous systems. / Doctor of Philosophy / Multiphase systems, such as a mixture of oil and water, are of great interest due to their ability to exhibit a multitude of properties from one material. Minimizing the size of the phases, through a technique called compatibilization, often improves the properties of the material. A common example is salad dressing, where the oil phase is compartmentalized into microscopic particles using surface-active molecules known as surfactants. Surfactants, also known as amphiphiles, partition to the interface between different phases due to the surfactants being comprised of dissimilar molecular constituents. One way to generate polymeric amphiphiles, where a polymer is a large molecule comprised of a molecular chain of repeating units, is through synthesizing block copolymers. Block copolymers have blocks of different constituents that are colocalized through covalent bonds in the polymer backbone and often exhibit phase separated structures, allowing for enhanced transport properties such as is seen in membranes. Using semi-crystalline polymers in membranes allows for enhanced mechanical integrity, as the crystallites act as physical crosslinks, or tie points, similar to the knots in a 3D rope ladder. These molecular knots limit the distance that the linear segments of the rope ladder can stretch, which in membranes leads to reduced swelling and increased mechanical performance. In this work we use semi-crystalline polymers to generate blocky copolymers through the use of halogenation. Halogenation installs halogen moieties as pendant groups on the polymer backbone, which can then by used as a chemical handle for subsequent reactions to further incorporate functionality into the copolymer and achieve desired properties such as proton (hydrogen nuclei) transport in fuel cell membranes. Halogenation also allows for the generation of blocky semi-crystalline copolymers for compatibilizing polymer blends of materials like poly(tetrafluoroethylene) and poly(ether ether ketone). Also in this work, we discuss the additive manufacturing of mechanically reinforced elastomers. An elastomer is another type of crosslinked network, and a mechanically reinforced elastomer can be through of as a 3D rope ladder where some of the linear segments of rope are replaced with steel bars, thus increasing the amount of work required to deform the network. The last multiphase systems discussed are similar to salad dressing, where there is a continuous water phase and a microscopic particle phase. The microscopic particles in this work are amphiphilic block copolymers that change their solubility in water with temperature and also have functionalities that should allow for the binding of metals from water-based systems.

In the presented thesis thin praseodymia films on non-passivated and passivated Si(111) substrates were investigated. The first part deals with PDA of praseodymia films with fluorite structure under UHV conditions in the temperature region from RT to 600°C. Here, a sophisticated model of the annealing process of praseodymia films is established. This is done by detailed analysis of XRD measurements using the kinematic diffraction theory in combination with the analysis of GIXRD, XRR and SPA-LEED measurements. It is shown that the untreated films, which are oxidized in 1 atm oxygen to obtain fluorite structure, do not exhibit pure PrO2 stoichiometry as it was assumed before. Instead, they decompose into two laterally coexisting species exhibiting a PrO2 and a Pr6O11. oxide phase, respectively. These species are laterally pinned to the lattice parameter of bulk Pr6O11. Homogeneous oxide films with Pr6O11 phase can be observed after annealing at 100°C and 150°C. Here, lateral strain caused by the pinning of the species is minimized and an increase of the crystallite sizes is determined. If higher annealing temperatures are applied, the film decomposes again into two coexisting species. Finally, after annealing at 300°C, a mixed crystalline film with both Pr2O3 and Pr2O3+Delta oxide phases is formed, where Delta denotes a considerable excess of oxygen within the sesquioxide phase. Again the lateral strain increases due to the tendency of praseodymia phases to increase their lattice parameters during oxygen loss combined with the lateral pinning. This is accompanied by a decrease of crystallite sizes, which are afterwards comparable to those of the untreated films. Further annealing at temperatures above 300°C does not significantly change the structure of the oxide film. However, the increase of the amorphous Pr-silicate interface between Si substrate and oxide at the expense of the crystalline oxide can be observed after annealing at higher temperatures. Furthermore, an increased mosaic spread of the crystallites occurs, which reduces the lateral strain caused by the oxygen loss. Nevertheless, the crystalline structure is stable against further annealing up to temperatures of 600°C. Transportation of the sample under ambient conditions after annealing at 200°C and 300°C leads to the formation of an additional crystalline structure at the surface which cannot be allocated to any praseodymia phase and may be explained by the contamination of the topmost crystalline layers with Pr-hydroxides. The results obtained from praseodymia films annealed in 1 atm nitrogen show that these films are good candidates to form homogeneous oxide films with pure cub-Pr2O3 structure by subsequent annealing in UHV. Here, a single oxide species is already observed after annealing at 300°C by SPA-LEED measurements which is in contrast to praseodymia films with fluorite structure where higher annealing temperatures (600°C) are necessary. In this case, negative effects like interface growth or increased defect density (mosaics, grain boundaries) can be minimized. Investigations on oxygen plasma-treated praseodymia films to obtain pure PrO2 stoichiometry are presented in the second part. Oxygen plasma-treated samples are compared with samples oxidized in 1 atm oxygen regarding the structure of the crystalline film. For this purpose, XRR and XRD measurements are performed to get structural information of the oxide film, which can be used to identify the corresponding oxide phases. Here, significantly smaller lattice constants of the crystalline oxide species can be observed after plasma treatment, which points to the incorporation of additional oxygen atoms. This verifies former studies, where a higher oxidation state of the oxide film was found by XPS measurements and it shows that plasma-treated films exhibit a higher oxidation state than films oxidized in 1 atm oxygen due to the availability of reactive atomic oxygen in the plasma. Furthermore, the Pr-silicate interface between crystalline film and Si substrate is not increased during plasma treatment. In the last part of the presented thesis, first results from the epitaxy of praseodymia films on Cl-passivated Si substrates are shown. The aim is to suppress the Pr-silicate formation during the growth process. Thus, praseodymia films are grown on passivated and non-passivated substrates to compare the crystallinity of both samples using XSW and LEED measurements. The structure of the oxide films on Cl-passivated Si is determined afterwards by XRR. It is shown that crystalline films with cub-Pr2O3 structure and several nanometer thickness can be successfully grown on Cl-passivated substrates. Here, the Pr-silicate interface layer are restricted to a single mono-layer. In contrast, the films grown on non-passivated substrates are completely amorphous containing Pr-silicates and Pr-silicides.

Current strategies for designing biomaterials involve creating materials and interfaces that interact with biomolecules, cells and tissues.  This thesis aims to investigate several bioactive surfaces, such as nanocrystalline diamond (NCD), hydroxyapatite (HA) and single crystalline titanium dioxide, in terms of material synthesis, surface functionalization and characterization. Although cochlear implants (CIs) have been proven to be clinically successful, the efficiency of these implants still needs to be improved. A CI typically only has 12-20 electrodes while the ear has approximately 3400 inner hair cells. A type of micro-textured NCD surface that consists of micrometre-sized nail-head-shaped pillars was fabricated. Auditory neurons showed a strong affinity for the surface of the NCD pillars, and the technique could be used for neural guidance and to increase the number of stimulation points, leading to CIs with improved performance. Typical transparent ceramics are fabricated using pressure-assisted sintering techniques. However, the development of a simple energy-efficient production method remains a challenge. A simple approach to fabricating translucent nano-ceramics was developed by controlling the morphology of the starting ceramic particles. Translucent nano-ceramics, including HA and strontium substituted HA, could be produced via a simple filtration process followed by pressure-less sintering. Furthermore, the application of such materials as a window material was investigated. The results show that MC3T3 cells could be observed through the translucent HA ceramic for up to 7 days. The living fluorescent staining confirmed that the MC3T3 cells were visible throughout the culture period. Single crystalline rutile possesses in vitro bioactivity, and the crystalline direction affects HA formation. The HA growth on (001), (100) and (110) faces was investigated in a simulated body fluid in the presence of fibronectin (FN) via two different processes. The HA layers on each face were analysed using different characterization techniques, revealing that the interfacial energies could be altered by the pre-adsorbed FN, which influenced HA formation. In summary, micro textured NCD, and translucent HA and FN functionalized single crystalline rutile, and their interactions with cells and biomimetic HA were studied. The results showed that controlled surface properties are important for enhancing a material’s biological performance.

Le besoin pour des biocapteurs à haute sensibilité mais simples à préparer et à utiliser est en constante augmentation, notamment dans le domaine biomédical. Les cristaux colloïdaux formés par des microsphères de polymère ont déjà prouvé leur fort potentiel en tant que biocapteurs grâce à l’association des propriétés des polymères et à la diffraction de la lumière visible de la structure périodique. Toutefois, une meilleure compréhension du comportement de ces structures est primordiale avant de pouvoir développer des capteurs efficaces et polyvalents. Ce travail propose d’étudier la formation et les propriétés des cristaux colloïdaux résultant de l’auto-assemblage de microsphères de polymère en milieu aqueux. Dans ce but, des particules avec différentes caractéristiques ont été synthétisées et caractérisées afin de corréler les propriétés des particules et le comportement de la structure cristalline. Dans un premier temps, des microsphères réticulées de polystyrène anioniques et cationiques ont été préparées par polymérisation en émulsion sans tensioactif. En variant la quantité de comonomère chargé, le chlorure de vinylbenzyltriméthylammonium ou le sulfonate styrène de sodium, des particules de différentes tailles, formes, polydispersités et charges surfaciques ont été obtenues. En effet, une augmentation de la quantité du comonomère ionique permet de stabiliser de façon électrostatique une plus grande surface et de diminuer ainsi la taille des particules. Cependant, au-dessus d’une certaine concentration, la polymérisation du comonomère en solution devient non négligeable, provoquant un élargissement de la distribution de taille. Quand la polydispersité est faible, ces microsphères chargées, même celles non parfaitement sphériques, peuvent s’auto-assembler et former des cristaux colloïdaux diffractant la lumière visible. Il semble que les répulsions électrostatiques créées par les charges surfaciques favorisent la formation de la structure périodique sur un grand domaine de concentrations et améliorent leur stabilité en présence de sel. Dans un deuxième temps, le besoin d’un constituant stimulable nous a orientés vers les structures cœur-écorce. Ces microsphères, synthétisées en deux étapes par polymérisation en émulsion sans tensioactif, sont formées d’un cœur de polystyrène et d’une écorce d’hydrogel. Différents hydrogels ont été utilisés afin d’obtenir des propriétés différentes : le poly(acide acrylique) pour sa sensibilité au pH, le poly(N-isopropylacrylamide) pour sa thermosensibilité, et, enfin, le copolymère poly(N-isopropylacrylamide-co-acide acrylique) donnant une double sensibilité. Ces microsphères forment des cristaux colloïdaux diffractant la lumière visible à partir d’une certaine concentration critique et pour un large domaine de concentrations. D’après les changements observés dans les spectres de diffraction, les stimuli ont un impact sur la structure cristalline mais l’amplitude de cet effet varie avec la concentration. Ce comportement semble être le résultat des changements induits par la transition de phase volumique sur les interactions entre particules plutôt qu’une conséquence du changement de taille. Les interactions attractives de van der Waals et les répulsions stériques sont clairement affectées par la transition de phase volumique de l’écorce de poly(N-isopropylacrylamide). Dans le cas des microsphères sensibles au pH, les interactions électrostatiques sont aussi à considérer. L’effet de la concentration peut alors être mis en relation avec la portée de ces interactions. Finalement, dans l’objectif futur de développer des biocapteurs de glucose, les microsphères cœur-écorce ont été fonctionnalisées avec l’acide 3-aminophénylboronique afin de les rendre sensibles au glucose. Les effets de la fonctionnalisation et de la complexation avec le glucose sur les particules et leur empilement périodique ont été examinés. La structure cristalline est visiblement affectée par la présence de glucose, même si le mécanisme impliqué reste à élucider. / The need for biosensors with high sensibility but simple preparation and use has been increasing, especially in the biomedical field. Crystalline colloidal arrays (CCAs) formed by polymer microspheres have already demonstrated great potential for biosensing applications, combining the polymer properties to the visible light diffraction caused by their periodic structure. However, a better understanding of the behavior of such structures is essential in the objective to develop efficient and versatile biosensors. This work proposes to investigate the formation and properties of CCAs created by the self-assembly of polymer microspheres in aqueous medium. For that purpose, particles with different features have been synthesized and studied to highlight the correlation between the properties of the particles and the behavior of the CCAs. First, anionic and cationic cross-linked polystyrene microspheres have been prepared by surfactant-free emulsion polymerization. Different sizes, shapes, polydispersities and surface charge densities have been obtained by the use of various amounts of charged comonomers, either vinylbenzyltrimethylammonium chloride or sodium styrenesulfonate. Indeed, an increasing amount of the ionic comonomer leads to a decreasing particle size because of the ability to electrostatically stabilize more surfaces. However, above a certain concentration, the polymerization of the comonomer in solution increases the polydispersity of the particle size. When allowed by a low polydispersity, the charged microspheres can self-assemble into CCAs with intense visible light diffraction, even for particles not quite spherical. It appears that the electrostatic repulsions created by the charges help in the formation of the periodic structure over a wide range of particle concentrations and improve their stability towards ionic strength. Secondly, the need for a sensitive component brought us to investigate core-shell structures. These microspheres, synthesized by a two-step surfactant-free emulsion polymerization, are made of a polystyrene core and a hydrogel shell. Different hydrogels have been used to achieve different properties: poly(acrylic acid) for pH-sensitivity, poly(N-isopropylacrylamide) for thermosensitivity and poly(N-isopropylacrylamide-co-acrylic acid) for double sensitivity to both stimuli. Above a certain critical concentration, and over a wide range of concentrations, these microspheres also form CCAs with visible light diffraction. The resulting crystalline structures also display a response to the stimuli, visible through changes in the diffraction spectra, but the response appears to be dependent on the microsphere concentration. This behavior seems to be the result of a change in the interactions between particles rather than the outcome of the volume change of the particles. Attractive van der Waals and repulsive steric interactions are clearly affected by the temperature-induced volume phase transition of poly(N-isopropylacrylamide) microspheres. In the case of pH-sensitive, electrostatic interactions are also to be considered. The effect of concentration can then related to the range of the interactions. Finally, in the objective to develop glucose sensors, the previous microspheres have been functionalized with 3-aminophenylboronic acid to make them responsive to glucose. The effects of the functionalization and complexation with glucose on the particles and their CCAs have been investigated. The crystalline structure is clearly affected by the presence of glucose, even though the mechanism involved remains to be clarified.

Nous avons étudié in situ et en temps réel la structure de grains du silicium multi-cristallin issue de la solidification dirigée en utilisant l’imagerie X synchrotron. La radiographie X permet de suivre l’évolution de l’interface solide/liquide et de caractériser sa dynamique et sa morphologie. La topographie X nous donne des informations sur la structure de grains formée, les contraintes et les défauts issus de la solidification. Nous avons montré l’importance la préparation de l’état initial de la solidification en particulier pour les expériences de reprise sur germe. L’analyse de la morphologie de l’interface solide/liquide nous a permis de caractériser la surfusion cinétique du front de solidification, de comprendre l’évolution des sillons de joints de grains et d’analyser les mécanismes de compétition de grains ainsi que de révéler l’impact des impuretés sur la structure de grains formée à l’issue de la solidification. Le phénomène de maclage a aussi été observé dans nos expériences et nous avons démontré que les macles dans le silicium multi-cristallin peuvent être des macles de croissance. Deux types de macles ont été identifiés et le phénomène de compétition de grains en présence de macles étudié. / We studied in situ and real-time the grain structure of multi-crystalline silicon from directional solidification using synchrotron X-ray imaging techniques. X-ray Radiography gives information on the evolution, dynamics and morphology of the solid/liquid interface. X- ray Topography gives more information on the grain structure, strains and defects that occur during solidification step. We showed the importance of the preparation of the initial stage of solidification in particular in the experiments where solidification is initiated from seed. The analysis of the solid/liquid interface morphology allowed us to characterize the kinetic undercooling of the solidification front, to understand the evolution of the grains boundary grooves and to analyze the mechanisms of grain competition and also to reveal the impurities impact on the grain structure formed at the end of the solidification. We also observed twinning phenomenon in our experiments and we demonstrated that twins in multi-crystalline silicon can be growth twins. Two kinds of silicon twins have been identified and the grain competition phenomenon with twins studied.

Ce travail concerne l'étude du polymorphisme, de la dynamique et des transitions de phases de cinq dérivés de l' adamantane : 1-fluoroadamantane, 1-adamantaneméthanol, 1,3-diméthyladamantane, 1,3-dibromoadamantane et 1,3-adamantanediol.Les diagrammes pression -température ont été établis pour la majorité de ces dérivés. Ces matériaux peuvent présenter une, voire plusieurs, transitions de phases. Le 1-fluoroadamantane, le 1,3-diméthyladamantane et le 1,3-adamantanediol possèdent une phase plastique avant fusion.Les structures de toutes les phases non plastiques ont été résolues principalement à partir de diagrammes de diffraction des rayons X sur poudre. Celles du 1,3-dibromoadamantane, et du 1,3-diméthyladamantane sont ordonnées. L'existence d'un désordre statistique concernant l'occupation du site d'un atome a été montrée pour les autres phases. L'atome de fluor du 1-fluoroadamantane peut occuper 4 (phases III et II) ou 8 sites (phase I). Dans le cas de la phase I du 1-adamantaneméthanol et de la phase II du 1,3-adamantanediol, la symétrie du réseau implique que l'atome d'hydrogène lié à l'oxygène se partage sur deux sites.Deux mécanismes de transition ordre-désordre par une relation de groupe à sous-groupe ont été montrés pour le cas du 1-fluoroadamantane et du 1-adamantaneméthanol en utilisant des techniques expérimentales complémentaires (DSC, DRX, RAMAN, GSH...). Le paramètre d'ordre de la transition résulte de la variation continue en fonction de la température de l'inclinaison du dipôle C-F pour le premier et, de la diminution de l'angle beta de la phase monoclinique jusqu'à 90°, pour le second.La dynamique moléculaire dans le cas du 1-fluoroadamantane a été étudiée par spectroscopie diélectrique. L'existence d'une double relaxation associée à deux mouvements de réorientations compatibles avec le réseau et la symétrie a été révélée. / This work deals with the study of the polymorphism, dynamics and phases transitions of five adamantane derivatives : 1-fluoroadamantane, 1-adamantanemethanol, 1,3-dimethyladamantane, 1,3-dibromoadamantane and 1,3-adamantanediol.Pressure-Temperature phase diagrams have been established for the majority of these derivatives. These materials may have one or more phase transitions. Plastic phases are observed before melting for 1-fluoroadamantane, 1,3-dimethyladamantane and 1,3-adamantanediol.The structures of all the non plastic phases have been solved, mainly from powder X-ray diffraction patterns. It is shown that 1,3-dibromoadamantane and 1,3-dimethyladamantane structures are ordered. Statistical disorder concerning the occupation of the site of one atom has been revealed in the other structures. The fluorine atom in 1-fluoroadamantane has four (phase III and II) or eight (phase I) possible equivalent sites. Due to the crystal symmetry of 1-adamantanemethanol (phase I ) and 1,3-adamantanediol (phase II), the hydrogen atom related to the oxygen atom is spitted on two sites.Two mechanisms of continuous order-disorder transitions through a group-subgroup relationship have been shown for the case of 1-fluoroadamantane and 1-adamantanemethanol using complementary experimental techniques (DSC, XRD, RAMAN, SHG ...). The order parameter of the transition results, by a continuous variation of the orientation of the C-F dipole for the first and, for the second, the continuous variation of the beta monoclinic angle down to 90°.Molecular dynamics in the case of 1-fluoroadamantane has been studied using dielectric spectroscopy. We have highlighted the existence of a double relaxation associated with two movements of reorientations compatible with the network and the symmetry.

La perméabilité aux gaz et aux liquides des matériaux polymères est une propriété qui est mise à profit dans de nombreux domaines industriels. Cette thèse est effectuée dans l'optique de mieux appréhender la problématique de l'étanchéité des conduites flexibles par les polymères. Ainsi, les perméabilités de H2S, CO2 et CH4 dans le polyéthylène (PE) ont fait l'objet d'une étude effectuée dans le contexte de cette thèse. La perméabilité est une propriété qui résulte de la solubilisation des gaz dans le polymère puis de la diffusion de ces produits à travers la matière. La solubilité, qui caractérise l’aptitude d’un gaz à pouvoir s’absorber dans le polymère, est une propriété d’équilibre, qui pourra être étudiée par les techniques de Monte Carlo. La diffusion, qui caractérise l’aptitude d’un gaz à se mouvoir plus ou moins rapidement dans le réseau polymère, sera quant à elle, étudiée par dynamique moléculaire. Au dessous de la température de fusion, le polyéthylène est à l'état semi-cristallin. Cet état est composé de régions contenant des chaînes orientées aléatoirement (régions amorphes) et des régions contenant des chaînes orientées sur un réseau (régions cristallines). La morphologie complexe des polymères semi-cristallins présente des hétérogénéités de dimensions nanométriques, ce qui est difficilement accessible par la simulation moléculaire. A fin d'étudier la solubilité et la diffusion de gaz dans le polyéthylène semi-cristallin, nous modéliserons uniquement la phase amorphe au cours de ce travail. Par contre, l’effet des régions cristallines sur la phase amorphe sera pris en compte dans la simulation par une contrainte ad-hoc. / The gas permeability through the polymers is a property that is exploited in many industrial fields. The objective of this thesis is to better understand the problem of sealing of flexible pipes with polymers. Thus, the permeability of H2S, CO2 and CH4 in polyethylene (PE) was studied during this work. Permeability is a property resulting from the dissolution of gases in the polymer and then diffusion of these products through the material. Solubility, which characterizes the ability of a gas to be absorbed in the polymer, is a property of equilibrium, which can be studied by Monte Carlo techniques. Diffusion coefficient, which characterizes the ability of a gas to move more or less rapidly into the polymer network, will in turn studied by molecular dynamics.Below the melting temperature, polyethylene is in semi-crystalline state. This state is composed of regions containing randomly oriented chains (amorphous regions) and regions containing chains oriented regularly on a network (crystalline regions). The complex morphology of semi-crystalline polymers has nanometric heterogeneities, which is not easily accessible by molecular simulation. In order to study the solubility and diffusion coefficient of gases in semi-crystalline polyethylene, we model only the amorphous phase in this work. However, the effect of crystalline regions on the amorphous phase will be taken into account in the simulation by an ad-hoc constraint.

La mousse métallique a des propriétés mécaniques et thermodynamiques uniques qui pourraient s'avérer utiles dans de nombreux domaines, tels que la construction légère et ingénierie automobile. Cependant, la mousse métallique n'est pas encore établie en génie.Une des raisons sont les difficultés et les prix élevés dans le processus de fabrication. Causée par drainage gravitaire en état liquide, peuvent se produire des distributions de matériel non homogènes. En outre, dépassant le drainage peut provoquer rupture de bulle et la génération de soufflures. Ces effets négatifs potentiellement peuvent être évités en ajoutant magnétique ou champs électromagnétiques au cours du processus de génération.Dans cette thèse, l'influence de ces champs est donc étudié en réalisant la phase de résolution des simulations. Ces simulations sont effectuées avec le code interne premier. Une modification de la modélisation de la collision était nécessaire pour enquêter sur l'agglomération de bulles dans le métal liquide.Calcul d'une configuration statique-drainage, les mécanismes de l'agglomération sont étudiés sans la présence de champs électriques ou magnétiques. Aux vitesses élevées de drainage, les bulles flottent. À des vitesses inférieures de drainage, les bulles s'agglomèrent dans la partie supérieure du domaine, formant des structures cristallines compacte.La préférence expérimentalement bien connue de commande cubes axés sur le visage, plus hexagonale compacte vous passez votre commande de volume égal bulles est reproduit numériquement. Appliquant davantage des simulations et expériences, un mécanisme de l'instabilité de la commande de façon hexagonale compacte est identifié, ayant pour résultat la préférence de commande de cubes axés sur le visage.Afin de déterminer les propriétés mécaniques de la mousse métallique solide avec la fraction de gaz faibles et aux fonctionnalités avantageuses et désavantageuses d'état d'arrangements de bulle, simulations par éléments finis de la mousse métallique solide avec cavités sphériques sont réalisées et comparées. Une influence significative de la quantité de cristaux de bulle sur la mécanique de la mousse se trouve. Le type de l'ordre cristallin est moins important.On étudie l'influence d'un champ magnétique horizontal sur l'agglomération de bulle. La résistance de drainage peut être augmentée sensiblement en ajoutant un champ magnétique. La structure résultante des bulles est moins sensible à un champ magnétique.Combinant un courant électrique horizontal et une perpendiculaire, champ magnétique horizontal se traduit par une force verticale de Lorentz. Cette force peut équilibrer la gravitation et donc, provoquer la rotation des bulles. Simuler cet État révèle une distribution homogène de bulle. Dans le même temps, friser les champs de force dans le voisinage de chaque bulle induire un mouvement continu en remuant. Petit champ électromagnétique forces n'empêchent pas les bulles d'agglomération, mais peuvent varier le montant de la commande cristallisé et par conséquent, les propriétés mécaniques de la mousse solide qui en résulte.En conclusion, un champ magnétique horizontal augmente la résistance de drainage, tandis que sa combinaison avec un courant électrique provoque des distributions de bulle homogène et peut modifier la structure de la mousse et la fraction de gaz. Les résultats de cette thèse pourraient aider à améliorer le processus de fabrication industrielle de mousse métallique ou même permettre la production de métal poreux avec la fraction de gaz définie par l'utilisateur. / Metal foam has unique mechanical and thermodynamic properties which could prove useful in many fields, such as light-weight construction and automotive engineering. However, metal foam is not yet established in engineering. One reason are the difficulties and high prices in the fabrication process. Caused by gravity-driven drainage in liquid state, inhomogeneous material distributions can occur. Also, exceeding drainage might cause bubble rupture and the generation of blow-holes. These negative effects potentially can be avoided by adding magnetic or electromagnetic fields during the generation process. In this thesis, the influence of these fields is therefore investigated by conducting phase resolving simulations. These simulations are carried out with the in-house code PRIME. A modification of the collision modelling was necessary in order to investigate the agglomeration of bubbles within liquid metal. Computing a static-drainage setup, the agglomeration mechanisms are investigated without the presence of electric or magnetic fields. At high drainage velocities the bubbles float. At lower drainage velocities the bubbles agglomerate in the upper part of the domain, forming close-packed crystalline structures. The experimentally well known preference of face-centred cubic ordering, over hexagonally close-packed ordering of equal-volume bubbles is reproduced numerically. Applying further simulations and experiments, an instability mechanism of hexagonally close-packed ordering is identified, resulting in the preference of face-centred cubic ordering. In order to determine the mechanical properties of solid metal foam with low gas fraction and to state advantageous and disadvantageous features of bubble arrangements, Finite-Element simulations of solid metal foam with spherical voids are carried out and compared. A significant influence of the amount of bubble crystals on the foam mechanics is found. The type of the crystalline ordering is less important. The influence of a horizontal magnetic field on the bubble agglomeration is investigated. The drainage resistance can be increased significantly by adding a magnetic field. The resulting structure of the bubbles is less sensitive to a magnetic field. Combining a horizontal electric current and a perpendicular, horizontal magnetic field results in a vertical Lorentz force. This force can balance gravitation and thus, cause rotation of the bubbles. Simulating this state reveals a homogeneous bubble distribution. At the same time, curling force fields in the vicinity of each bubble induce a continuous stirring motion. Small electromagnetic field strengths do not prevent the bubbles from agglomerating, but can vary the amount of crystallized ordering and therefore, the mechanical properties of the resulting solid foam. In conclusion, a horizontal magnetic field increases the drainage resistance, while its combination with an electric current causes homogeneous bubble distributions and can alter the foam structure and the gas fraction. The results of this thesis could help improve the industrial fabrication process of metal foam or even allow production of porous metal with user-defined gas fraction.

Neste trabalho, foram depositadas sobre lâminas de silício camadas de zeólitos cristalinos, formados por cadeias de átomos de zinco e bases conjugadas do imidazol (ZIF: Zeolitic Imidazolate Framework), com o objetivo de avaliar os processos de adsorção e absorção do CO2 e aplicar essas camadas como pré-concentradores para a detecção de CO2. Para a deposição das camadas ZIF através dos processos Spinning e casting, foi proposta uma solução química alternativa que emprega etanol como solvente em vez de metanol como reportado na literatura, a fim de proporcionar um processo menos tóxico ao ser humano e viabilizar o armazenamento de CO2 para aplicações envolvendo não apenas a sua detecção mas também a sua remoção do ambiente. As camadas ZIF foram depositadas utilizando uma solução obtida a partir da mistura de nitrato de zinco (4,3g) e 2-metilimidazol (9,7g) em etanol com diversas diluições com a finalidade de variar o pH na faixa de 7,2 a 8,2. Como resultado, verificou-se que as camadas obtidas apresentaram estrutura cristalina ZIF-8 ou ZIF-90 apenas na situação de pH próximo de 7. Além disso, as camadas depositadas através da técnica Spinning apresentaram baixa aderência sobre lâminas de silício e não foi possível depositar camadas com espessuras na faixa de micrômetros. Por outro lado, camadas repetitivas com aproximadamente 7, 5µm de espessura foram depositadas nas lâminas de silício através do processo casting em solução de pH = 7,2 (50ml). Após o recozimento dessas camadas na temperatura de 150 ºC por 48h em ambiente de nitrogênio ultrapuro, obtiveram-se distribuições repetitivas de nanocristais com tamanhos na faixa de 5 a 400nm e estrutura cristalina tipo ZIF-90. Das medidas de espectroscopia IR nas camadas de ZIF-90, observou-se que a banda localizada em 2337cm-1 intensifica com o aumento da pressão do CO2 e com o tempo em que a pressão é mantida. Além da banda em 2337cm-1, foi observada uma segunda banda em 2360cm-1, indicando dois diferentes tipos de resposta: (i) a banda em 2337cm-1 foi associada a uma porção substancial de moléculas de CO2 absorvidas dentro da camada junto aos contornos dos nanocristais ou dentro da sua estrutura cristalina, e (ii) a banda em 2360cm-1 foi atribuída à porção de moléculas de CO2 adsorvidas na superfície. Além disso, se o tempo de exposição da camada de ZIF-90 ao CO2, na pressão atmosférica for de pelomenos 2h, atinge-se sensibilidade de 100ppm ao CO2, considerando a leitura mínima de absorbância como sendo igual a 0,02 para 0,5 l/min de CO2 fluindo sobre a amostra. / In this work, layers of crystalline zeolites formed by chains of zinc atoms and conjugate bases of the imidazole (ZIF: zeolitic Imidazolate Framework) were deposited to evaluate the desorption and absorption of CO2 and apply these layers as pre-concentrators for CO2 detection. For the deposition of ZIF layers by means of spinning or casting, it was proposed an alternative chemical solution which employs ethanol as solvent instead of methanol, as reported in the literature, to provide a less toxic process to humans and allow one the CO2 storage applications involving not just detection but also its removal from the environment. The ZIF layers were deposited using a solution prepared from a mixture of zinc nitrate (4.3g) and 2-methylimidazole (9.7g) with several dilutions in ethanol to vary the pH in the range of 7.2 to 8.2. As a result, the crystalline structure of the layers was ZIF-8 or ZIF-90 only for pH next to 7. Furthermore, the layers deposited by spinning showed low adhesion to the silicon wafers and it was not possible to deposit layers for thickness in the micrometer range. Moreover, repetitive layers of approximately 7.5µm in thickness were deposited on the silicon wafers by casting for pH = 7.2 (50ml). After annealing these layers at a temperature of 150 ºC for 48h in ultra-pure nitrogen, it was obtained repetitive nanocrystals with size distributions in the range of 5 to 400 nm having a ZIF-90 crystal structure. From infrared (IR) measurements of the ZIF-90 layers, it was observed a band located at 2337cm-1 that increases with the increase of the CO2 pressure and with the exposure time to this pressure. In addition to the band at 2337cm-1, it was observed a second band at 2360cm-1 indicating two different responses: (i) the band at 2337cm-1 is related to a substantial portion of the CO2 molecules absorbed into the layer along the contours of the nanocrystals or within the crystal structure and (ii) the band at 2360cm-1 is related to the portion of CO2 molecules adsorbed on the surface. Also, if the ZIF-90 layer is exposed to CO2 at atmospheric pressure for at least 2h, a 100ppm sensitivity to CO2 is achieved considering the minimum absorbance as being 0.02 when 0.5 l/min of CO2 is flowing on the sample.