Polymers of various types are added to crude oils and oil products to prevent wax deposition, break water-in-oil emulsions, reduce drag in pipelines and to stabilize asphaltenes. In mixtures where a polymer does not adsorb on colloids, two stable liquid phases can arise due to depletion flocculation. Asphaltenes in heavy oils and toluene mixtures form sterically stabilized colloidal particles. In this work, the addition of a non-adsorbing polymer (polystyrene) to C5 Maya asphaltene + toluene mixtures was investigated experimentally and theoretically. As concentrated asphaltene + toluene mixtures are opaque to visible light, phase volumes and compositions were detected using ultrasound. The sensors comprised two commercial 64 element phased-array acoustic probes. The operation of the view cell, and kinetic and equilibrium data processing procedures were validated using mixtures of methanol + alkanes. Acoustic speed and attenuation profiles were found to provide independent measures of phase separation. At equilibrium, acoustic speed profiles are uniform in each phase with a step change at the interface. Acoustic wave attenuation profiles exhibit a sharp peak/spike at liquid-liquid interfaces. Mixtures of asphaltenes + polystyrene + toluene are shown to exhibit liquid-liquid phase behavior over broad ranges of composition. This is the first report of liquid-liquid phase behavior for such mixtures. One phase is asphaltene rich and the other phase is polystyrene rich. Liquid-liquid critical points were also identified along the liquid-liquid/liquid phase boundary for mixtures with two mean molar masses of polystyrene. Compositions of co-existing phases were computed using phase volume variations along dilution lines, acoustic speed data and a mass balance model. A parameter was introduced to improve the agreement between calculated and experimental speeds of sound. The results of the model indicate that more than half of the asphaltenes, by volume, participate in the depletion flocculation process. Phase compositions were measured independently using UV-visible spectrophotometry. The nominal size of asphaltene colloidal particles participating in the phase separation mechanism was estimated by comparing calculated phase boundaries with the experimental phase diagram. The estimated size of asphaltene colloidal particles is in agreement with the expected size of asphaltenes in toluene mixtures obtained exogenously. / Chemical and Materials Engineering

Friction forces between protein / polyelectrolyte layers, adsorption properties of proteins, and conformational changes due to variation in electrolyte concentration have been investigated. The aim was to obtain better understanding of adsorbed layer properties, with focus on the relation between layer structure and lubrication capabilities. The major techniques used were AFM (atomic force microscope) with colloidal probe for normal force and friction measurements together with QCM-D (quartz crystal microbalance with dissipation) for measurement of adsorption and conformational changes of adsorbed layers. A comparison between some techniques for calibration of the AFM instrument for friction measurements was made to find the most suitably one for colloidal probe friction measurements in aqueous solutions. It is suggested that the normal and torsional Sader methods are preferred in combination with torsional detector sensitivity measurement, for which one new methodology has been proposed. Adsorption was studied for bovine serum albumin, cytochrome c, myoglobin and mucin, whereas conformational changes of the adsorbed layer were monitored only for mucin. It was found that it was essential to take into account bulk density and viscosity changes for correct interpretations of QCM data when studying the effect of changes in electrolyte type and concentration on preadsorbed layers of mucin, and also when having different (high) concentrations of proteins in the measuring solution. The adsorbed amount of proteins appears to depend on the strength of the surface attachment, in such a manner that a too high affinity reduces the adsorbed amount. Friction properties in aqueous solution have been studied for adsorbed layers of PEO45MEMA:METAC co-polyelectrolytes, with varying density of grafted PEO45 side chains and varying charge density, as well as for a naturally occurring polyelectrolyte (chitosan) and the glycoprotein mucin. These polymers were used to cover a wide range of different types of adsorbed layers and interactions to gain a better understanding of friction mechanisms and demands on layer properties for achieving favourable lubrication. It was found that the common features of low friction layers are that no attractive forces are present, and that excluded volume and / or electrostatic forces counteract chain interpenetration under load. / QC 20100903

Starch is a mixture of two polysaccharides, amylose (AM) and amylopectin, which occurs naturally in the form of microscopic granules that are abundantly found in tubers, roots, cereal grains and fruits. In order to bring out their functional properties as thickeners and texture enhancers, starch granules are often disrupted by heating in excess water. This process, which is referred to as gelatinisation, causes the granules to swell and exude a fraction of the starch polysaccharides, resulting in a dramatic increase in the viscosity of the starch suspension. Surfactants are known to affect the different aspects of the gelatinisation process and, in particular, the swelling properties of starch. Surfactants are also known to form helical inclusion complexes with AM, the formation of which plays an important role in many of the instances in which starch and surfactants interact. This work was carried out in order to gain insight into how the surfactant structure (head group and chain length) influences the swelling properties of starch and the molecular mechanisms behind these effects. The investigations involved the study of the temperature-induced gelatinisation of starch in the presence of surfactants as well as studies on the association of surfactants to AM in solution and the solubility of the resulting AM-surfactant complexes. Information on the extent of granule swelling upon heating was indirectly obtained by means of viscometry while insight on the molecular events taking place during gelatinisation was sought by means of differential scanning calorimetry (DSC) and confocal laser scanning microscopy (CLSM). Viscometric studies revealed that, with the exception of the cationic surfactants (alkyl trimethyl ammonium bromides), short-chain (C10, C12) surfactants induce an early swelling (swelling at lower temperatures than the control sample) in normal wheat starch granules, whereas their longer chain counterparts (C14, C16) have the opposite effect. Contrary to this finding, the effect of surfactants on the swelling of waxy wheat starch granules, an AM-free starch variety, is not influenced by the surfactant chain length but by the head group charge of the surfactant. The enhancing/restricting effect of surfactants on the swelling of normal wheat starch is not correlated to their effect on the early aspects of gelatinisation (onset of the gelatinisation transition) but is, in most cases, associated with the dissociation temperature of AM-surfactant complexes formed simultaneously as the granules gelatinise. CLSM studies revealed that, compared to a longer-chain surfactant (C16), a short-chain (C12) surfactant has the ability to penetrate further into the granule matrix during gelatinisation, which may favour its availability for interacting with different starch granule components during gelatinisation. Studies on the interactions between AM and surfactants with different chain length (C12 vs. C16) and head group (sodium sulphates vs. maltosides) revealed that the presence of a charged head group favours the water solubility of the resulting AM-surfactant complexes. However, this effect can be counteracted by the effect of the surfactant chain length: an increase in the chain length (C12 vs. C16) decreases the solubility of the complex. / QC 20100913

Colloid displacement lithography is proving to be very effective in the designing of nanometer scale electronic devices. Precise control of the structure of matter at the nanometer scale has brought a revolutionary change in science and technology. The use of these nanometer scale devices ranges from the diagnosis of various diseases to cell repair to ultra strong materials. This research focused on optimizing the conditions for gold colloid particle adsorption for colloid displacement lithography, an expansion on gold colloid particle manipulation techniques using a scanned probe microscope. The system consists of a scrupulously cleaned glass surface that is coated with poly(diallyldimethylammonium chloride) (PDDA) and then with 5- or 10- nm gold colloid particles. The optimum conditions include the use of very low molecular weight PDDA (Avg MW <100,000 g/mol) or low molecular weight PDDA (Avg MW 100,000-200,000 g/mol) with an exposure time to the glass substrate of 120 to 150 minutes. This is then followed by a 24-hour exposure to the colloid solution. An atomic force microscope (AFM) is used to pattern the thus prepared colloid coated slides. In this work a variety of salts are used as potential blocking agents to prevent or modify the colloid adsorption. These include potassium iodide, potassium bromide, potassium chloride, sodium fluoride, sodiumsulfate, potassium hydrogen phosphate, potassium hydrogen phthalate, and sodium citrate. In summary, the following were found as a result of this work: The optimum conditions that lead to efficient patterning are: Low molecular weight PDDA with a coating time of 120 to 150 minutes. Exposure to 5-nm gold colloid for 24 hours The most interesting potential blocking agents are the phosphate, sulfate and citrate salts, as they show some potential for modifying the adsorption of the gold colloids on the PDDA. The dispersion of the colloid particles on the PDDA does not change when using the potential blocking agents compared to direct adsorption on the unmodified PDDA layer. The use of the potential blocking agents reduces the force required to pattern by a factor of 100 to 300.

No description available.

The surface force apparatus (SFA) has been an important technique for making direct force measurements and has contributed enormously to our understanding of colloidal interactions. The conventional SFA has been limited to measuring forces between solid surfaces, until recently when a modified SFA was developed at the Ian Wark Research Institute [1]. A fluid drop (mercury) is introduced into the apparatus which allows a range of deformable surfaces to be studied in the SFA. This project is an extension of this technique. Interactions between a mica sheet and a mercury drop are studied, including the modification of mercury with self-assembled monolayers (SAMs) of thiol surfactants, and the drop deformation due to non-equilibrium adsorption effects and hydrodynamic forces.

L’objectif de ce projet était l’étude systématique des interactions, de la microstructure et de la dynamique de suspensions de colloïdes qui imitent les mouvements de systèmes auto-propulsés (actifs), au moyen de techniques de diffusion : diffusion des rayons X aux (ultra) petits angles (USAXS/SAXS) et spectroscopie de corrélation de photons X (XPCS).À la différence des colloïdes passifs conventionnels (particules browniennes), les colloïdes actifs sont des systèmes hors équilibre faits d’objets auto-propulsés. Ces systèmes montrent une dynamique fascinante qui s’apparente aux mouvements de volée d'oiseaux, d’essaim d’insectes, etc.Les micro-organismes mobiles sont des exemples types de colloïdes actifs, notamment certaines variétés de bactéries, ou les colloïdes de type Janus caractérisé par une composition asymétrique de leur surface qui peux engendrer une propulsion, l’auto-diffusiophorèse. Les thèmes principaux de cette thèse sont les interactions inter-particule, les interactions particule-solvant et les dynamiques phorétiques des systèmes actifs.En premier lieu, la structure et la mobilité de la bactérie Escherichia coli ont été étudiées au moyen de SAXS/USAXS . Comme projet secondaire, l’obtention de données couvrant une très large gamme de vecteur de diffusion (q) a permis de dériver un modèle structural multi-échelle de la bactérie, en combinant les caractéristiques de colloïdes (corps cellulaire), de membranes (enveloppe cellulaire) et de polymères (flagelles). Ce modèle a été affiné au moyen de mesures complémentaires de diffusion de neutrons aux petits angles (SANS) sur des suspensions de la bactérie E. coli en variant le contraste externe (remplacement isotopique partielle du solvant) afin d’aboutir à une détermination quantitative de la densité électronique des membranes et des distances entre membranes.Ces bactéries ont ensuite été utilisées comme éléments actifs en mélange avec des colloïdes passifs de silice de taille sub-micrométrique, pour comprendre comment la présence de bactéries actives mobiles affecte les interactions effectives et la dynamique des colloïdes passifs. Des mesures USAXS et XPCS simultanées ont permis de déduire les propriétés statiques et hydrodynamiques de ces colloïdes passifs. Les données suggèrent que les bactéries actives se comportent comme un fluidifiant pour les colloïdes passifs, en réduisant leurs interactions attractives et en augmentant leur dynamique ; réciproquement, ces derniers sont affectés par la solution tampon et par la présence de bactéries augmente la viscosité environnante effective.Enfin, les mouvements phorétiques de colloïdes de silice et de type Janus (silice partiellement recouvert de nickel) suspendus dans un mélange de 3-methylpyridine (3MP) + eau/eau lourde pendant la séparation de phase liquide-liquide ont été investigués par USAXS et XPCS. Les mouvements des colloïdes sont fortement corrélés à la dynamique de la séparation de phase du fait de l’absorption préférentielle de 3MP à la surface de silice. Les colloïdes de silice montrent une dynamique advective avec une diffusion amélioré en direction des microdomaines riches en 3MP, évoquant la dynamique des systèmes auto-propulsés, jusqu’à l’aboutissement de la séparation de phase. Les suspensions de colloïdes de type Janus ont un comportement beaucoup plus complexe, la dynamique étant fortement corrélée aux interactions asymétriques avec le solvant. Cette dynamique est soit augmentée soit supprimée en fonction de la concentration en 3MP qui modifie aussi la micro-structure du système. Au lieu que les colloïdes de silice migrent vers la phase riche en 3MP, les colloïdes de type Janus agissent comme des tensioactifs en se plaçant à l’interface.Cette thèse démontre l’intérêt des techniques de diffusion pour explorer les propriétés des systèmes actifs et examiner leur comportement en thermodynamique hors équilibre afin de compléter les informations obtenues par observations microscopique. / This project aimed to systematically investigate the interactions, microstructure and dynamics in suspensions of colloidal particles that mimic active motions, using (Ultra) Small- Angle X-ray Scattering (USAXS/SAXS) and X-ray Photon Correlation Spectroscopy (XPCS). As opposed to the conventional passive colloids (Brownian particles), active colloids are non-equilibrium systems consisting of self-propelled particles that display many fascinating dynamics, such as streaming, swarming, flocking, etc. in appropriate media. Practical examples of active systems are motile microorganisms, such as some species of bacteria, or synthetic Janus colloids – characterized by an asymmetric chemical composition of their surface – that can induce a propulsion mechanisms, like self-diffusiophoresis. The foci of this thesis are on interparticle interactions, particle-medium interactions and the phoretic dynamics in active systems.Firstly, the structure and motility of Escherichia coli bacteria were investigated by combined USAXS and SAXS methods. As an offshoot, the scattering data spanning a broad scattering vector (q)-range permitted the derivation of a multiscale structural model by combining colloidal (cell-body), membrane (cell-envelope) and polymer (flagella) features. This model was further refined by contrast-variation Small Angle Neutron Scattering (SANS) measurements on E. coli suspensions at three match points and the full contrast which allowed the determination of the membrane electron-density and the inter-membrane distances on a quantitative scale.These bacteria were then used as active component in a mixture with micron-sized passive silica colloids, with the aim of investigating how the effective interactions and dynamics of passive colloids are affected by the presence and the motility of active E. coli. Both static and hydrodynamic information were obtained via the simultaneous use of USAXS and XPCS techniques. Data suggested active bacteria act as a fluidizing agent in such systems, reducing attractive interactions and enhancing the dynamics of passive colloids, which, at the same time, are affected by the buffer and more viscous environment due to the bacterial presence.Finally, the phoretic motions of micron-sized silica colloids and half-coated silica/nickel Janus colloids suspended in a mixture of 3-methylpyridine (3MP) and water/heavy water undergoing liquid-liquid phase separation were investigated using USAXS and XPCS. Due to the preferential wetting of 3MP on the silica surface, the motion of the colloids is strongly correlated to the dynamics of phase separation.Silica colloids displayed advective motion with enhanced diffusion toward the 3MP-rich phase reminiscent of self-propelled motion until the phase separation is completed. Suspensions of Janus colloids showed a much richer scenario, where colloid dynamics are strongly influenced by the asymmetric interactions with the solvent. The dynamics of Janus colloids were either enhanced or suppressed depending on the 3MP concentration, which, concurrently, affected the microstructure of the system. As opposed to the partitioning in 3MP-rich phase in the case of silica colloids, Janus particles behave like surfactants at the interface.The thesis demonstrates the ability of studying active systems by means of scattering methods and probe their behaviour in the thermodynamic limit and complement the information derived from direct microscopy observations.

This thesis presents an investigation of pH-responsive, redox-sensitive poly(MMA-co- MAA) and poly(EA-co-MAA) hollow particles for the repair of load-bearing soft tissues, such as articular cartilage and the intervertebral disc. Hollow particles continue to attract major interest due to their numerous potential applications. The new method for hollow particle preparation presented in this thesis does not require the use of a colloidal template and is well suited for scaling up. Hollow particles were formed using linear poly(MMA-co-MAA) and poly(EA-co-MAA) aliphatic copolymers synthesised using free-radical chain copolymerisation performed in solution. These copolymers were dissolved in dichloromethane using methanol as a cosolvent and emulsified in water. Diffusion of the methanol into the aqueous phase prompts precipitation of the copolymer at the droplet/water interface. The more hydrophobic copolymers containing less MAA showed improved morphology compared to copolymers containing more MAA. Also, poly(EA-co-MAA) hollow particles had a more spherical morphology than poly(MMA-co-MAA) hollow particles with equivalent MAA contents. This was attributed to the lower Tg of the EA structural monomer, which resulted in more flexible particle shells. Unusually, during potentiometric titration of uncrosslinked hollow particles, the pH of the system decreased with increasing neutralisation. This behaviour is thought to be due to the unfolding of copolymer chains, exposing shielded carboxyl groups. The random structure of the copolymers is believed to be necessary for this behaviour. Crosslinked particles became swollen when the pH was increased using buffers. Concentrated dispersions formed self supporting gels, due to steric confinement, at 5 wt.%. The crosslinking process was performed by functionalising with cystamine using carbodiimide chemistry. This introduced disulphide crosslinks; which could be cleaved under reducing conditions at high pH, dissolving the gels. This ability to reduce the hollow particle shells to their constituent linear copolymer chains gives potential for natural removal from the body via extraction by the renal system. pH-triggered loading and release of a hydrophilic dye using crosslinked hollow particles was demonstrated. The similarity of the particle formation process to traditional solvent evaporation also allowed the loading of a hydrophobic dye. However, these particles were not crosslinked so release following swelling could not be investigated. Cystamine-crosslinked systems suffered from degradation due to thiol-disulphide exchange at high pH (~ pH 8). Crosslinking of one system was performed using 2-amino ethyl methacrylate (AEM). This introduced covalent, vinyl intra-shell crosslinking; which did not break down at high pH. Additional AEM was also used to allow inter-particle UVcrosslinking to form doubly crosslinked (DX) hollow-particle hydrogels. These gels did not re-disperse in buffer. To our knowledge, this is the first example of a covalent hydrogel formed from pH-responsive hollow particles. The DX gels offer improved mechanical properties compared to the singly crosslinked, physical gels. Freeze-dried samples of all of the gels produced during this study showed highly porous structures when observed using SEM. The rapid diffusion of FITC-dextran through a sample of DX gel indicates that these pores were interconnected. This is beneficial as it encourages tissue ingrowth, in addition to allowing the rapid diffusion of nutrients, oxygen and cell waste in vivo.

In this project we aim to produce a thermally triggered PLGA particulate gel, which is injectable and biocompatible. This will act as a scaffold for soft tissue repair. Three coating polymers were tested: Pluronics (PEG-PPG-PEG), poly(PPGMA-co-PEGMA) and poly(PNIPAm-DMA+). These were first tested as a dilute solution for clouding behaviour and then added to PLGA nanoparticles dispersions and tested rheologically for gel behaviour. These three polymers were chosen for their amphiphilic nature which may allow for surface attachment and decreasing miscibility with temperature. The PLGA copolymer in this work contained 75% lactic acid and 25% glycolic acid, and was made into a nanoparticle dispersion by interfacial deposition. The Pluronic L62 showed a promising cloud point temperature (Tclpt) of 37 °C, but did not show gel behaviour with the PLGA dispersions. It conferred thermally triggered aggregation, which may be useful as a drug delivery system. The poly(PPGMA-PEGMA) was synthesised using a free radical polymerisation feed method. These copolymers showed promising Tclpt values (20-37 °C) but only showed increased viscosity when heated at high concentration and when mixed with a PLGA dispersion. The structure-property relationships for these copolymers were analysed. Poly(NIPAM-DMA+) showed gelation at low concentrations without the particles, when the particle dispersion was added the gel maintained its strength up to 300% strain. This is unlike most particulate gels which tend to be brittle. Using cell culture the biocompatibility of these gels was tested. After 72 hours the cells appeared healthy and to be proliferating.

Au cours des vingt dernières années, les nanomatériaux (caractérisés par des dimensions de l’ordre de 10 à 100 nm) ont attiré une attention croissante de par leurs propriétés optoélectroniques uniques. C’est tout particulièrement vrai pour les nanomatériaux inorganiques, tels que les quantum dots, les nanoparticules métalliques ou encore les nanoparticules à base de silice. Par contre, l’étude des nanomatériaux obtenus à partir de molécules organiques est un domaine d’intérêt beaucoup plus récent. Cette thèse présente une étude détaillée de nanoparticules organiques fluorescentes originales et des nanostructures organiques préparées à partir de deux ou trois types de chromophores distincts (nanocomposites binaires et ternaires). En particulier, l'attention est focalisée sur la préparation, la caractérisation et la stabilisation de ces nouveaux nanomatériaux, ainsi que leurs applications dans le domaine biologique et de l’opto-electronique. / During the past two decades, increasing research attention has been devoted to nanomaterials (materials in the range of 10-100 nm) because of their unique optoelectronic properties. In particular, inorganic nanomaterials, such as quantum dots, metal-based nanoparticles and silica nanoparticles, have been investigated extensively. Instead, nanomaterials based on organic molecules are been subject of research only since very recent years. This thesis presents an extensive study of novel fluorescent organic nanoparticles and fluorescent organic binary and ternary nanoassemblies. In particular the attention is focused on the preparation and characterization of organic nanoparticles and new nanocomposites obtained from different types of small organic chromophores, their stabilization and the use of these materials for biological and optoelectronics applications.