"Swirling multiphase flows are found in a wide range of industrial processes. Such flows are used for separation of flows containing phases of different densities and for devices such as the spinning tensiometer. These flows are challenging to predict computationally, due to the presence of a phase boundary and the large pressure gradient generated by the swirl. In the present work the applicability of the front tracking method to swirling multi-phase flows is demonstrated by studying the evolution of a bubble in spinning tensiometer. Previous studies show that the evolution of a bubble in the spinning drop tensiometer can be used to measure the interfacial tension and other rheological properties. The front tracking method is applied to the spinning tensiometer problem to study several cases and verify the convergence of the solutions. The results are validated with other computational methods, theoretical models and experimental results. The length scales obtained from the front tracking method are in agreement with the corresponding values from experiments and other computational studies. The shape of the end of the elongated bubble obtained from the simulations is found to be similar to that suggested by a theoretical expression from previous studies. The simulations predict that the relaxation of bubble radius is exponential with time, at a rate that is found to be slightly greater than that predicted by the theoretical model."

Le principal objectif des travaux présentés dans ce manuscrit était d’étudier certains paramètres régissant l’efficacité et la durabilité de moustiquaires avec des molécules insecticides incorporées dans les fils de polyéthylène. Pour cela deux axes de travail ont été identifiés : l’étude des phénomènes de migration des molécules insecticide dans les fils de polyéthylène et l’étude des mécanismes de photo-dégradation de l’insecticide étudié : la deltaméthrine.L’étude de l’influence du procédé de fabrication des moustiquaires sur la morphologie du polyéthylène a permis de montrer que l’étape d’étirage à froid était critique dans la définition des propriétés morphologiques (cristallinité et orientation de la structure cristalline) et mécaniques des fils. L’effet du recuit observé est plus modéré (légère augmentation de l’épaisseur des lamelles cristallines). Néanmoins, il a été montré que les modifications induites par le recuit sur la morphologie du polyéthylène ont une influence sur les phénomènes de migration des molécules insecticides dans les fils. En effet, alors qu’un retard est observé dans les courbes de désorption des fils non recuits, ce retard disparaît pour les fils recuits. Il a été également montré que la faible vitesse d’évaporation de la deltaméthrine permet de limiter la migration de la deltaméthrine hors des fils.L’étude de la photo-dégradation de la deltaméthrine a permis de mettre en évidence les principaux mécanismes de dégradation (isomérisation, scission de la fonction ester et de la fonction cyclopropane). L’ajout d’additifs de type antioxydants ou filtres UV permet de limiter la vitesse de dégradation de la deltaméthrine / The main objective of the works presented in this manuscript was to study some of the parameters ruling the efficacy and the durability of the mosquito nets with incorporated insecticide in the polyethylene yarns. To achieve this goal, two lines of research were identified: the study of the insecticide migration phenomena in the yarns and the study of the photodegradation mechanisms of the molecule of interest: the deltamethrin.The study of the influence of the nets fabrication process on the polyethylene morphology showed that the cold-drawing step was critical to define the morphological (crystallinity and orientation of the crystalline structure) and mechanical properties. The observed influence of the heat-setting appeared less important (slight increase of the crystalline lamellae thickness). However, the heat-setting induced modifications which affected the migration of the insecticide molecules in the yarns. Indeed, while a delay is observed in the desorption curves of the non-heat-set yarns, this time-lag disappeared in the heat-set yarns. It was also shown that the low evaporation rate of deltamethrin permits to impede the migration of deltamethrin out of the yarns.The study of the photodegradation of deltamethrin permitted to highlight the main degradation mechanisms (isomerization, ester cleavage and cyclopropane cleavage). Antioxidant and UV absorber additives can be used to reduce the deltamethrin degradation rate

The efficacy of dispersed reduced graphene oxide (rGO) as a nucleation site for the growth of mesophase in an isotropic pitch was investigated and quantified in this study. Concentrations of rGO were systematically tested in an isotropic petroleum and coal-tar pitch during thermal treatments and compared to pitch without rGO. The mesophase content of each thermally treated pitch was quantified by polarized light point counting. Further characterization of softening temperature and insolubles were quantified. Additionally, the pitches with and without rGO were melt spun, graphitized, and tensile tested to determine the effects of rGO on graphitized fiber mechanical properties and fiber morphology.

The main aim of this thesis work is to investigate the electrical, optical and thermal impact characteristics of cobalt oxide doped antimony tin oxide (CoO-ATO) in the form of thin films and nanofiber membranes. CoO-ATO is a novel composite material that has the potential to be used as reinforced aircraft coatings, military garment coatings, or more specifically as an anti-reflective (AR) top coating for photovoltaic (PV) cells. This work will be critical in determining the effectiveness of using a CoO-ATO layer in these applications. Electrospun nanofibers and spin coated thin films consisting of a polymeric solution of CoO-ATO will be used. Thin films are created using spin coating techniques, and nanofiber membranes are created using an electrospinning technique. Polystyrene (PS) will be used as a solute, and chloroform as a solvent, to create the solution. It is hypothesized that coatings of this material will have improved optical characteristics as compared to traditional ATO coatings and minimum impact from thermal cycling making it a favorable candidate for PV cells. This work will do an electrical, optical and thermal cycling impact characterization of CoO-ATO thin films and nanofiber membranes for a doping range of x% CoO where x ranged from 0.2

Stimuli responsive coatings offer a versatile method by which to manipulate interfacial interactions of proteins in a desired way. However, there exists little guidance as to how the structure of a responsive polymer coating influences adsorption of proteins. In this dissertation, the adsorption behavior of immuglobulin G (IgG) on poly (N-isopropylacryamide) (PNIPAAm) hydrogel coatings was investigated as a function of film thickness. PNIPAAm exhibits a hydrophilic to hydrophobic transition above a critical temperature of ~32°C in aqueous solutions. In this research, through the use of quartz crystal microbalance with dissipation (QCM-D) it was observed that the adsorption was thickness dependent and became non-reversible as the temperature was decreased. Interestingly, QCM-D results also suggested a similar amount of protein adsorption on both hydrated and dehydrated PNIPAAm surfaces. A rigid film analysis using Sauerbrey equation revealed a multi-layer formation on the collapsed PNIPAAm coatings. Although it is allegedly reported that PNIPAAm favors adsorption above the critical temperature due to hydrophobic interactions, there have been several studies that reported adsorption of proteins below the critical temperature. To better understand the QCM-D results, hydrodynamic shear force assays in a spinning disk configuration were performed in order to quickly measure and quantify adhesion of polystyrene (PS) probe spheres (10μm) to the PNIPAAm coatings in both the solvated (hydrophilic) and collapsed (hydrophobic) state. The influence of polymer coating thickness, polymer chain cross-link density, microsphere concentration and adsorption time on the adhesion characteristics of the coatings was investigated in relation with volume phase transition of the polymer coatings. A series of experiments on quantification of the temperature dependent adhesion of proteins adsorbed on surface attached PNIPAAm coatings of thicknesses was performed as the surface chemistry was switched from hydrophilic to hydrophobic. First, adhesion of polystyrene (PS) microspheres on PNIPAAm coatings was quantified in order to have a guideline for temperature dependent adhesion performance of these coatings. PS particles were subjected to a range of detachment shear stresses through hydrodynamic flow in a spinning disk configuration. These experiments provide an indirect method to determine the force of adhesion since it is proportional to the hydrodynamic force. Model protein, IgG, was then linked to PS microspheres and the mean adhesion strength of the IgG coated PS microspheres were determined through the detachment shear stresses. The influence of PS deposition time, PS bead concentration, PNIPAAm coating thickness and PNIPAAm cross-link density on the adhesion strength were addressed. The results indicated that in the collapsed state, the adhesion of bare hydrophobic PS microspheres depends strongly on coating thickness. For hydrophilic charged PS microspheres the adhesion was always higher on the hydrated PNIPAAm surfaces and appeared not to be strongly affected by the increase in PNIPAAm coating thickness. The adhesion of IgG was higher on the collapsed PNIPAAm surfaces and the adhesion trend did not significantly change as the PNIPAAm film thickness was increased. For PNIPAAm coatings with the cross-link density reduced by factor of 10, the adhesion was again higher on the collapsed PNIPAAm surface and scaled linearly with thickness. Moreover, the influence of thickness became prominent at the higher thickness values (165 nm-185 nm). In addition, the adhesion of carboxylated microspheres on PNIPAAm did not reach equilibrium and increased linearly with microsphere deposition time. A study on the sensing characteristics of PNIPAAm coatings in response to heavy metal ions was also conducted in this dissertation. The temperature-dependent swelling behavior of poly(N-isopropylacrylamide) and tripeptide Gly-Gly-His/poly(NIPAAm) conjugate hydrogel coatings were investigated using a quartz crystal microbalance with dissipation (QCM-D) while in contact with NaCl, ZnCl2, NiCl2, and CuCl2 solutions. To fabricate the tripeptide conjugated gels, precursor gels of poly(NIPAAm-co-3-aminopropylmethacrylamide[3.5 mole%]) were synthesized via free radical polymerization. The metal binding tripeptide, Gly-Gly-His, was subsequently synthesized in the gel via a Merrifield solid phase peptide synthesis (SPPS) technique, in which the amino group of the copolymer gel provided a functional site to support peptide synthesis. It was found that the logarithm of the transition temperature of the tripeptide Gly-Gly-His/poly(NIPAAm) conjugate hydrogel was proportional to the ionic strength, showing two distinct regions at low and high ionic strengths for the divalent ions. In the low ionic strength regime, the salting out constants were 0.08 M-1, 0.07 M-1, and 0.06 M-1 for Cu2+, Ni2+, and Zn2+, respectively, which follows the known trend for binding of the ions to Gly-Gly-His. In the high ionic strength region, when the metal-ion binding sites in the tripeptide conjugate hydrogel were saturated, the salting out constants were similar to the salting out constants associated with pure poly(NIPAAm).

« La solidification rapide : relation Elaboration – Microstructure et Propriétés d'un alliage » RESUME Si les propriétés intrinsèques des matériaux dépendent de la force des liaisons chimiques, qui ne peuvent être modifiées, il est bien connu que leurs propriétés extrinsèques dépendent de la microstructure. Les métallurgistes disposent de moyens techniques pour contrôler relativement bien cette microstructure et aussi faire en sorte que les propriétés associées correspondent aux besoins du cahier des charges de l'application. Classiquement, partant du lingot élaboré par fusion, des traitements thermomécaniques plus ou moins complexes engendrent la microstructure. Mais il est bien clair que les possibilités d'évolution de la microstructure dépendent dramatiquement de l'état initial de l'alliage. C'est ici qu'interviennent les techniques basées sur la solidification rapide. Elles vont engendrer des microstructures initiales pouvant être très différentes de celles qui sont conventionnelles, et qui pourront, par traitements thermomécaniques, aboutir à des microstructures finales également très différentes. Les méthodes de solidification rapide d'alliages métalliques ou céramiques ont pour but principal d'étendre ou de modifier les limites des domaines d'équilibre thermodynamique, ou d'obtenir de nouvelles structures atomiques, ce qui n'est généralement pas accessible par des méthodes dites conventionnelles de solidification. Les produits élaborés se caractérisent par exemple par réduction de taille de grains, par la précipitation d'une phase secondaire plus fine et homogène Ces procédés permettent dans le même temps d'obtenir les matériaux directement à partir de l'état fondu, sous la forme de produits minces finis ou dans un état intermédiaire, tels que des rubans (10 à 80 μm) par « planar flow casting PFC » (flot planaire), des tôles fines (de 200 μm à 3 mm d'épaisseur (en production industrielle) par « twin roll casting TRC» (coulée entre rouleaux) ou encore mais plus rarement des fils (100 à 200 μm de diamètre) par « In rotating water melt spinning INROWASP». J'ai dans ce manuscript décrit les méthodes et techniques d'élaboration que j'utilise en développant quelques aspects thermodynamiques et cinétiques tout en révélant l'essentiel des informations techniques. Un ensemble d'exemples tirés de mes travaux en collaboration et dans le cadre de projets de recherche internes au laboratoire, nationaux et internationaux illustrent ces techniques, notamment les verres métalliques massifs, les quasicristaux, les alliages à magnétorésistance géante, et particulièrement les alliages à mémoire de forme. Les relations entre d'une part la méthode de préparation, qui inclut la technique de fusion, de solidification, les traitements associés thermo-mécaniques, et d'autre part les caractéristiques structurales, microstructurales ainsi que les propriétés mécaniques et fonctionnelles ont été mises en évidence. Le choix de méthodes de production par solidification rapide, comme je l'ai écrit, peut dans certaines conditions autoriser l'obtention d'une phase qu'on ne peut pas obtenir par refroidissement classique (< 103 KS-1) ou, par l'abaissement de la taille de grains, optimiser certaines caractéristiques mécaniques. Néanmoins comme le montrent certains résultats mitigés sur les alliages à mémoire de forme, ces méthodes ne sont en aucun cas une panacée aux problèmes rencontrés comme le manque de ductilité à température ambiante. Le problème de la mise en forme à froid qu'on rencontre dans nombres d'alliages intermétalliques ou les verres métalliques ne sont pas ou seulement partiellement résolus par ces procédés. Mais la production en une seule ou un nombre limité d'étapes d'objets finis ou semi-finis reste un élément économique appréciable de ces méthodes. Les phases quasicristallines stables thermodynamiquement ainsi que les verres métalliques massifs ne nécessitent pas des vitesses de refroidissement supérieures à 103 KS-1 et peuvent être obtenus par des méthodes de préparation ce qui nécessite certaines précautions (c.a.d. par exemple sans contamination chimique) mais à vitesse de refroidissement classique. Néanmoins dans ce cas il a été démontré que seule une méthode de solidification rapide (telle que le melt spinning ou l'atomisation gazeuse) permet d'une part d'obtenir la précision compositionnelle requise et d'autre part d'atteindre, après traitement thermique, une qualité structurale de la phase optimale (cas des quasicristaux). En ce qui concerne les verres métalliques ces techniques nous permettent d'étudier plus facilement la capacité à l'amorphisation, la formulation et la déformation à froid de ces alliages : par exemple les essais de nanoindentations sur les rubans ou les tôles hypertrempées qui nous autorisent à remonter aux mécanismes de déformation des alliages massifs. L'obtention d'une précipitation de dispersoïdes nanométriques dans la matrice amorphe (VMM) ou la matrice paramagnétique des alliages magnétorésistifs à l'étude, n'est possible qu'en utilisant ces techniques.

Numerous publications are available on the structure and properties correlation of fibers spun from polymers with flexible chains such as polyethylene terephthalate (PET), nylon, polypropylene. Also considerable amount of work is reported in fibers spun from rigid rod polymers like poly(p-phenylene terephthalamide) due to their value in high performance fibers category. However, very limited literature is available on the structure-properties relationship in fibers manufactured from poly(phenylene sulfide) (PPS), a high performance polymer which possesses chain flexibility between above two classes of polymers. A few researchers have studied crystallization kinetics and the fibers by extruding the polymer using capillary rheometers. However, there is a lack of in-depth study of conversion of PPS into fibers through melt spinning and further enhancement of properties by drawing and annealing experiments. The purpose of the present research was to fill this void by systematically studying the fiber manufacture from PPS polymers. Four variances of proprietary Fortron® linear PPS resins differing in MW were analyzed for their characteristics such as molecular weight (MW) and MW distribution (MWD) using gel permeation chromatography (GPC), rheological properties using melt flow indexer (MFI) and capillary extrusion rheometer, and crystallization kinetics using differential scanning calorimetry (DSC). The fibers were spun on a pilot melt spinning facility, using a multi-hole spinneret, under different processing conditions. As-spun fibers were drawn and annealed subsequently by varying draw-annealing conditions. Thorough characterization of the as-spun and drawn-annealed fibers was carried out using various analytical techniques such as tensile testing, DSC, polarized light optical microscopy (POM), wide angle X-ray scattering (WAXS), and small angle X-ray scattering (SAXS). Relationship between polymer characteristics, process conditions and structure-properties in the fibers was analysed statistically. A strong correlationship between polymer molecular weight, processing conditions during melt spinning and draw-annealing, processing behavior during melt spinning and drawing, fiber tensile properties and fiber morphology is reported herein. Interaction effects of material and process variables in evolving fiber structure and properties are also discussed. Through optimal combination of material and process variables, PPS fibers of tenacity close to six gpd were obtained. With the help of several characterization tools listed earlier, melting behavior of PPS polymers and fibers is decoded, and probable structural model of high tenacity PPS fibers is proposed.

Tissue engineering is a multidisciplinary field that is rapidly emerging as a promising new approach in the restoration and reconstruction of tissues. In this approach, three dimensional (3D) scaffolds are of great importance. Scaffolds function both as supports for cell growth and depot for sustained release of required active agents (e.g. enzymes, genes, antibiotics, growth factors). Scaffolds should possess certain properties in accordance with usage conditions. Wet-spinning is a simple technique that has been widely used for the fabrication of porous scaffolds for tissue engineering applications. Natural polymers can effectively be used in scaffold fabrication due to their biocharacteristics. Among natural polymers, chitosan and alginate are two of the most studied ones in tissue engineering and drug delivery fields because of being biologically renewable, biodegradable, biocompatible, non-antigenic, non-toxic and biofunctional. In this study, two kinds of porous scaffolds were produced as chitosan and alginate coated chitosan fibrous scaffolds by wet-spinning technique In order to investigate the delivery characteristics of the scaffolds, loading of gentamicin as a model antibiotic and bovine serum albumin (BSA) as a model protein was carried out in different loading models. Resultant scaffolds were characterized in terms of their structural formation, biodegradation, biomineralization, water uptake and retention ability and mechanical properties. Additionally, release kinetics of gentamicin and BSA were examined. Efficiency of gentamicin on Escherichia coli (E.coli) was examined. Characterization of scaffolds revealed their adequacy to be used in bone tissue engineering applications and capability to be employed as bioactive agent delivery systems.

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This PhD thesis presents structural investigations of amorphous inorganic materials: oxide and oxynitride glasses and mesoporous bioactive glasses (MBGs), by solid-state Nuclear Magnetic Resonance (NMR). Lanthanum oxide and oxynitride [La-Si-(Al)-O-(N)] glasses have a large number of potential applications due to their physical properties. In our work we have studied, compared to previous investigations, significantly expanded ranges of glass compositions (for oxynitride glasses, including samples of very high nitrogen content, up to 53 % out of the anions). We have estimated local environments of 29Si and 27Al structural units (their coordination, polymerization degree and number of N incorporated into tetrahedral units) in the materials. We have suggested a random Al/Si distribution along with almost uniform non-bridging oxygen atoms distribution in aluminosilicate glasses. Silicon nitride was used as precursor in the oxynitride glass synthesis. We studied both α- and β-modifications of silicon nitride, 15N-enriched, as well as fully (29Si, 15N)-enriched samples. We have shown that the linewidths of 15N NMR spectra are dominated by J(29Si-15N) coupling in 29Si315N4 sample. Mesoporous bioactive glasses in the CaO-SiO2-P2O5 system show superior bioactivity (the ability to form a hydroxycarbonate apatite layer on the glass surface when exposed to body fluids) compared to conventional bioactive glasses due to their large surface area and uniform pore-size distribution. Previous studies suggested a homogeneous cation distribution over the MBG samples on a 10−20 nm length-scale. From our results, on the other hand, we may conclude that Si and P is not intimately mixed. We propose a structural model, in which the pore walls of MBGs are composed of a silica network, and a phosphate phase is present as nanometer-sized clusters that are dispersed on the pore wall.