Over fifty small sinkholes (~1 meter in depth and width) were found in conjunction with structural damage to homes in an area south of Cleveland, TX. The local geology lacks carbonate and evaporite deposits associated with normal sinkhole development through dissolution. The morphology and distribution of sinkholes, and the geologic setting of the site are consistent with piping erosion. However, the site lacked the significant hydraulic gradient or exit points for sediment associated with traditional piping erosion. In areas of sinkholes, geophysical measurements of apparent electrical conductivity delineated anomalously high conductivity levels that are interpreted as a brine release from a nearby oil-field waste injection well. The contaminated areas have sodium adsorption ratios (SAR) as high as 19, compared to background levels of 3. Sodium has been shown to cause dispersion of soil colloids, allowing for sediment transport at very low velocities. Thus, subsurface erosion of dispersed sediment could be possible without significant hydraulic gradients. This hypothesis is backed by the observation of the depletion of colloidal particles within the E-horizon of sinkholes. However, there is a lack of precedence of waste brines initiating colloid dispersion. Also, sodium dispersion is not thought to be an important process in piping erosion in humid settings such as this one. Therefore, laboratory experiments on samples from the site area, designed to simulate field conditions, were conducted to measure dispersion verses pH, SAR and electrical conductivity (EC). Analysis of the experimental data with neural networks showed that an increase in SAR did increase dispersion. A dispersion prediction map, constructed with the trained neural network and calibrated geophysical data, showed correlation between sinkhole locations and increased predicted dispersion. This research indicates that a contaminant high in sodium content has caused colloidal dispersion, which may have allowed nontraditional subsurface erosion to occur in an area lacking a significant hydraulic gradient.

Structure function changes of casein micelles were studied as a function of concentration using a non invasive concentration method, osmotic stressing. A combination of serum analysis, light scattering and rheological measurements were used to characterize the physico-chemical properties of casein micelles. In heated and unheated milk, rheological studies indicated that casein micelles behave as hard spheres of similar volume fractions, if the viscosity changes in the serum phase and the particle particle interactions are taken into account. The differences in the distribution of the heat induced complexes between colloidal and soluble phase affected the colloidal properties of casein micelles. Above 70 g L-1 protein, the protein particles were no longer free diffusing. Re-dilution of the suspensions showed no irreversible aggregation. The data suggested that in the range of concentration studied casein micelles behave as hard spheres. Age gelation was also investigated on heated and unheated concentrated milk. In unheated concentrated milk proteolysis played an important role in imparting an increase in viscosity by causing aggregation of the casein micelles. On the other hand, in heated milk, there was a significant effect of the whey protein aggregates, which increased their interaction with the casein micelles over time. This effect, together with proteolysis caused age gelation in heated concentrated milk. The method of concentration used in this research, osmotic stressing, was then compared to ultrafiltration. It was demostrated that these two methods are not equivalent, as shear and mixing during ultrafiltration cause rearrangements to the casein micells. The differences were clearly demonstrated by adding soluble caseins to the milk before or after concentration. This project brings a better understanding on the effects of concentration on the structure-function of casein micelles and the interactions occurring in milk proteins during concentration.

No description available.

The arrangement of soft materials through solution processing techniques is a topic of profound importance for next generation solar cells; the resulting morphology has a major influence on construction, performance and lifetime. This thesis investigates the connections between the soft matter physics of colloidal systems and solid state dye sensitised (SSDS) and bulk heterojunction (BHJ) solar cells. A study of aqueous titanium dioxide nanoparticulate suspensions was carried out in order to observe how suspension structure can be controlled by altering the inter-colloid potential via pH-induced electrostatic charging. Measurements were performed at volume fractions between 0.025% and 8.2% with the solution pH set to 3.1, 3.5 or 4.5 before mixing. Suspensions with a volume fraction above 4% formed self-supporting gels regardless of the set pre-mix pH. These gels displayed shear thinning behaviour with a power law exponent of 0.8, a yield stress of 11(1) Pa and rheological response consistent with an aggregated fractal network. At lower volume fractions, suspensions exhibited consolidation interpreted as the collapse of a gel of fractal clusters with a fractal dimension of 2.36. The velocity of the suspension/supernatant interface exhibited delayed sedimentation behaviour, as well as further fractal-based power law scalings with volume fraction. Lower volume fraction suspensions were explored using dynamic light scattering. Limited aggregation of ‘stable’ suspensions was observed when compared to primary aggregate radii measured from electron microscopy images. To connect suspension structure and cell manufacture, the behaviour of more concentrated suspensions was observed during the drying of thin films, a process which forms an essential part of a SSDS solar cell. Lowering the pH of the suspension after mixing from 4 to 3 resulted in an ordering of observed crack domains. An increase in film delamination was also observed. Rates of mass loss during drying followed the expected three phase process, although there was an unexpected increase in rate during the initial phase (where rate is usually constant in time). Dynamic light scattering was found to be a useful but demanding technique for studying cluster formation in titanium dioxide suspensions. A non-linear fitting technique utilising the method of moments was thoroughly explored using computer simulated datasets. The algorithm reduced the systematic error in fitted parameters for moderately polydisperse (0:2 < < 0:4) datasets as compared to the commonly applied linear algorithm. The fitting algorithm was also robust to bad initial estimates of parameters. Finally, test solar cells have been built using blends of titanium dioxide and poly-3-hexylthiophene. Device performance was reduced with blend standing time after mixing but could be improved by remixing the blend before spin coating, implicating a reversible process (e.g. aggregation of titanium dioxide or crystallisation of P3HT) in the loss of performance. Addition of a titanium dioxide hole blocking layer before spin coating reduced cell performance. Combining the above studies and these device designs provides a future platform for continuation of this work in the context of real devices.

Liquid crystals (LCs) are an interesting class of materials that are attracting significant attention due to their ever-growing applications in a wide variety of fields such as liquid crystal display (LCD) technology, materials science and bioscience. In recent years, along with the developments of materials at the nanoscale, doping LCs with nanoparticles (NPs) has emerged as a very promising approach for improving LC properties. Nanoparticle additives can introduce novel effects on optical and electro-optical properties of nematic liquid crystals (N-LCs), such as altered molecular alignment, faster response time and increased efficiency. This thesis studies the impacts that the inclusion of metallic NPs made of gold or semiconductor CdSe quantum dots (QDs), have on optical and electro-optical properties of N-LCs. Using polarized optical microscopy and detailed capacitance and transmittance measurements of nematic mixtures in electro-optic test cells, characteristics such as optical texture, phase transition temperatures, switching voltages and dielectric anisotropy are investigated in pure as well as doped samples. Surface ligands in NPs and their chemical functionalization play an important role in the LC-NP interactions, largely by determining the dispersibility of NPs and stability of the nanocomposites. One important objective of this thesis is to investigate and prepare a series of gold nanoparticles (Au NPs) with specially formulated robust coatings that maximizes solubility and stability in LC medium. Silanization of NPs is developed as a method to overcome the stability challenge. The functionalization of silanized NPs with aliphatic ligands or liquid crystalline molecules, provides chemically and thermally stable NPs with hydrophobic and structurally compatible surfaces required for dispersion in N-LCs. After complete characterization the synthesized particles are used to make the new nematic nanocomposites. By analysis of the structure-property relationships governing LC-nanomaterial composites and by comparison of new results and data from previous studies on other types of NPs, this thesis will further reveal the mechanism of the interrelations between host LC molecules and NP, considering the role of variables such as core composition, size and surface chemistry of NPs (e.g. siloxane shell, aliphatic ligand vs. liquid crystalline ligand) in achieving stable LC composites with desired optical and electro-optical properties.

The research presented in this dissertation explores the possibility of using colloidal indium tin oxide (ITO) nanoparticle solutions to direct write transparent conducting coatings (TCCs), as an alternative route for TCC fabrication. ITO nanoparticles with narrow size distribution of 5-7 nm were synthesized using a non-aqueous synthesis technique, and fabricated into films using spin coating on substrates made from glass and fused quartz. The as-coated films were very transparent (>95% transmittance), but highly resistive, with sheet resistances around 10¹³ Ω/sq . Pre-annealing plasma treatments were investigated in order to improve the electrical properties while avoiding high temperature treatments. Composite RIE treatment recipes consisting of alternating RIE treatments in O₂ plasma and in Ar plasma were able to reduce the sheet resistance of as spin coated ITO films by 4-5 orders of magnitude, from about 10¹³ Ω/sq in as-coated films to about 3 x 10⁸ Ω/sq without any annealing. Plasma treatment, in combination with annealing treatments were able to decrease the sheet resistance by 8-9 orders of magnitude down to almost 10 kΩ/sq , equivalent to bulk resistivity of ~0.67 Ω.cm. Investigation into effectiveness of various RIE parameters in removing residual organics and in reducing the sheet resistance of colloidal ITO films suggested that while reactive ion annealing (RIE) pressure is an important parameter; parameters like plasma power, number of alternating O₂-Ar RIE cycles were also effective in reducing the residual organic content. Impedance spectroscopy analysis of the colloidal ITO films indicated the dominance of the various interfaces, such as grain boundaries, insulating secondary phases, charge traps, and others in determining the observed electrical properties.

Nanometer-scale silicon shows extraordinary electronic and optical properties that are not available for bulk silicon, and many investigations toward applications in optoelectronic devices are being pursued. Silicon nanoparticle films made from solution are a promising candidate for low-cost solar cells. However, controlling the properties of silicon nanoparticles is quite a challenge, in particular shape and size distribution, which effect device performance. At present, none of the solar cells made from silicon nanoparticle films have an efficiency exceeding the efficiency of those based on crystalline silicon. To address the challenge of controlling silicon nanoparticle properties, both theoretical and experimental investigations are needed. In this thesis, we investigate silicon nanoparticle properties via quantum mechanical modeling of silicon nanoparticles and synthesis of silicon nanoparticle films via colloidal grinding. Silicon nanoparticles with shapes including cubic, rectangular, ellipsoidal and flat disk are modeled using semi-empirical methods and configuration interaction. Their electronic properties with different surface passivation were also studied. The results showed that silicon nanoparticles with hydrogen passivation have higher HOMOLUMO gaps, and also the HOMO-LUMO gap depends on the size and the shape of the particle. In contrast, silicon nanoparticles with oxygen passivation have a lower HOMO-LUMO gap. Raman spectroscopy calculation of silicon nanoparticles show peak shift and asymmetric broadening similar to what has been observed in experiment. Silicon nanoparticle synthesis via colloidal grinding was demonstrated as a straightforward and inexpensive approach for thin film solar cells. Data analysis of silicon particles via SEM images demonstrated that colloidal grinding is effective in reducing the Si particle size to sub-micron in a short grinding time. Further increases in grinding time, followed by filtration demonstrated a narrowing of the Si particle size and size-distribution to an average size of 70 nm. Raman spectroscopy and EDS data demonstrated that the Si nanoparticles contain oxygen due to exposure to air during grinding. I-V characterization of the milled Si nanoparticles showed an ohmic behaviour with low current at low biases then Schottky diode behaviour or a symmetric curve at large biases. / Graduate / 0794 / 0544 / zahraalbu@hotmail.com

Nanometer-scale silicon shows extraordinary electronic and optical properties that are not available for bulk silicon, and many investigations toward applications in optoelectronic devices are being pursued. Silicon nanoparticle films made from solution are a promising candidate for low-cost solar cells. However, controlling the properties of silicon nanoparticles is quite a challenge, in particular shape and size distribution, which effect device performance. At present, none of the solar cells made from silicon nanoparticle films have an efficiency exceeding the efficiency of those based on crystalline silicon. To address the challenge of controlling silicon nanoparticle properties, both theoretical and experimental investigations are needed. In this thesis, we investigate silicon nanoparticle properties via quantum mechanical modeling of silicon nanoparticles and synthesis of silicon nanoparticle films via colloidal grinding. Silicon nanoparticles with shapes including cubic, rectangular, ellipsoidal and flat disk are modeled using semi-empirical methods and configuration interaction. Their electronic properties with different surface passivation were also studied. The results showed that silicon nanoparticles with hydrogen passivation have higher HOMOLUMO gaps, and also the HOMO-LUMO gap depends on the size and the shape of the particle. In contrast, silicon nanoparticles with oxygen passivation have a lower HOMO-LUMO gap. Raman spectroscopy calculation of silicon nanoparticles show peak shift and asymmetric broadening similar to what has been observed in experiment. Silicon nanoparticle synthesis via colloidal grinding was demonstrated as a straightforward and inexpensive approach for thin film solar cells. Data analysis of silicon particles via SEM images demonstrated that colloidal grinding is effective in reducing the Si particle size to sub-micron in a short grinding time. Further increases in grinding time, followed by filtration demonstrated a narrowing of the Si particle size and size-distribution to an average size of 70 nm. Raman spectroscopy and EDS data demonstrated that the Si nanoparticles contain oxygen due to exposure to air during grinding. I-V characterization of the milled Si nanoparticles showed an ohmic behaviour with low current at low biases then Schottky diode behaviour or a symmetric curve at large biases. / Graduate / 0794 / 0544 / zahraalbu@hotmail.com

An improved crystallisation spectrometer has been designed, built and tested. It is to be used by others to gain new knowledge about the solidification of matter by study of the crystallisation of hard sphere colloid samples that are an established model for the behaviour of some aspects of atoms. In this crystallisation spectrometer, expanded and collimated green laser light is Bragg scattered from the colloidal crystals as they form, and the diffracted light is focused by a liquid filled hollow glass hemispherical lens onto low cost CCD array detectors that are rotated about the optical axis to average the intensities around the whole Debye-Scherrer cone of scattered light. The temperature of the sample is controlled to +/-0.1„a, and because of the ability to change the refractive index of the sample particles with temperature, this is utilised to control the amount of scattering from the sample Also, this spectrometer uniquely exploits the refractive index match of the colloidal particles, the solvent, the bath liquid, and the glass used for both the sample bottle and the hollow glass hemisphere. A unique facility has been incorporated to permit tumbling of the sample prior to the measurement commencing to shear-melt any pre-existing crystals. This ensures that the sample is completely fluid and is at the correct temperature at the start of the measurement. The instrument is assembled on an optical table and is computer controlled. Results presented show that this new spectrometer with its use of the whole Debye-Scherrer cone of Bragg scattered light and other enhancements gives insight into the crystallisation process more than one order of magnitude of time earlier than previous light scattering experiments, providing new knowledge about the crystallisation process.

This thesis reports on a comprehensive experimental study of the collective dynamics of colloidal hard sphere suspensions. The main quantity measured is the coherent Intermediate Scattering Function (ISF) using a range of techniques based on Dynamic Light Scattering (DLS). The collective dynamics are measured as a function of scattering vector for volume fractions spanning from dilute samples, through the fluid phase and the metastable region, up until deep in the glass region. This work describes two major explorations: (i) the effect of volume of fraction on the q-dependency of the collective dynamics; and (ii) a study of the ageing processes in colloidal glasses. The present work is unique in the application of several advanced experimental techniques, and in the level of averaging that has been carried out, enabling a more sophisticated analysis than has previously been possible. This includes the characterization of non-Fickian processes and the determinatio n of the current-current correlation function (CCCF) in the metastable fluid, and the quantitative characterization of the ageing process in the hard sphere glass. In addition, by combining aspects of the coherent and incoherent ISFs, this work also allows the expression of the collective dynamics in terms of the single particle displacement. The results show a dynamical change at the freezing point (f), which exposes the incapacity of the system to dissipate thermal energy via diffusing momentum currents, i.e. viscous flow. The structural impediments responsible for this, associated with dynamical heterogeneities, begin at the structure factor peak, and spread to other spatial modes as the volume fraction increases. Above the glass transition (g), structural relaxation becomes arrested at all spatial modes probed, i.e. flow is arrested. It is found that, following the quench, samples above the glass volume fraction approach some final