In the summer of 2008 (June 2nd September 19th) detailed measurements of meteorological conditions and glacier surface properties were conducted in the Belcher Glacier catchment (718 km2), Devon Island Ice Cap, Nunavut, Canada. These measurements were used to force and validate a distributed surface energy balance and sub-surface snow model capable of calculating surface ablation rates and meltwater runoff. This study represents a contribution to the International Polar Year (IPY) Glaciodyn project, whose overall aim is to examine the role of hydrology and ice dynamics in the response of marine-terminating glaciers in the Arctic to climate change. Spatially-averaged total water equivalent (w.e.) ablation was 677 mm w.e., and total predicted runoff during the 2008 summer was 3.9 x 108 m3. Net radiation (87%) was the main source of energy over the study period, followed by the sensible heat flux (13%). Net longwave radiation and the latent heat flux represented an overall energy loss from the surface. Modelled melt season duration lasted from June 17th August 15th, and the majority of ablation occurred in two main periods, from June 26th July 18th, and from July 27th to August 14th. Snowfall and lower air temperatures limited ablation between these dates and after August 15th. Ice exposure at elevations below 1000 m occurred by July 1st. Periods of high ablation rates were associated with positive air temperatures and high net shortwave radiation receipts, and with near surface air temperature gradients that were shallow or inverted (i.e. higher air temperatures at higher elevations). Periods of minimum ablation rates occurred when net shortwave radiation receipts were reduced (e.g. following summer snowfall) and when air temperatures were negative. The largest changes in both the net surface energy balance and ablation rates were linked to changes in surface albedo associated with (i) snowpack removal and ice exposure, and (ii) summer snowfall events. Modelled time series of runoff from individual sub-catchments within the Belcher catchment will be used to force a coupled hydrology and ice flow dynamics model of the Belcher Glacier that will be used to investigate the dynamic response of tidewater-terminating glaciers to surface hydrological forcing.

The focus of this thesis is fundamental surface force and friction studies of silica and cellulose surfaces, performed mainly with the atomic force microscope (AFM). The normal interactions between model cellulose surfaces have been found to consist of a longer range double layer force with a short range steric interaction, the nature of which is extensively discussed. Both the surface charge and range of the steric force depend on the type of cellulose substrate used, as does the magnitude of the adhesion. Studies of friction on the same surfaces reveal that surface roughness is the determining factor for the friction coefficient, with which it increases monotonically. The absolute value, however, is determined by the surface chemistry. The above is illustrated by studies of the effect of adsorbed xyloglucan, a prospective paper additive, which is found in the cell wall of all plants. Xyloglucan is like cellulose a poly- saccharide but the effect of its adsorption was to reduce the friction significantly, while following the identical trend with surface roughness. Xyloglucan also increases the adhesion between cellulose surfaces in a time dependent manner, interpreted in terms of a diffusive bridging interaction. These facts combined provide a mechanistic explanation to contemporaneous findings about xyloglucans benefit in paper strength and formation. In air, the adhesion between e.g. particles or fibres, must be at least partially determined by the formation of capillary condensates. The dependence of capillary condensation on relative humidity is however not yet fully understood so studies have been performed to cast light on this phenomenon. Above about 60 % relative humidity the adhesion and friction increase dramatically due to the formation of large capillary condensates. The extent of the condensates depends both on the time the surfaces equilibrate, but also on the surface roughness. Harvesting of the condensate during shearing is also observed through hysteresis of the friction-load relationship. Measurements of surface forces and friction in surfactant systems show a clear relation between the adsorbed surfactant layer and the barrier force and adhesion, which in turn determine the friction. All of these interactions are critically dependent on the composition of the surfactant solution. A mixed surfactant system has been studied consisting of a trimethylammonium cationic surfactant and a polyoxyethylene nonionic surfactant. The results are interpreted in terms of current theories of adsorption and synergistic interactions. Finally, a novel technique for the in situ calibration and measurement of friction with the AFM is proposed. Comparison with lateral measurements show that the approach is successful. / QC 20100920

Physical stress such as the surface roughness of the implants may activate the NFkB signalling pathway in macrophages. This activation is intimately related to the mechanism(s) by which the macrophage interacts with the surface through serum proteins and/or the formation of membrane rafts. This thesis examines the role of surface topography on activation of the NFkB signalling pathway in macrophages. We examined the effect of implant surface topography on activating the NFkB signalling pathway in the RAW 264.7 macrophage cell line. We also examined the effect surface roughness had on the adhesion of the macrophages using the different media. To finish, we observed the effect the different media and the surface roughness had on the morphology of the macrophages by Scanning Electron Microscopy. Activation of the NFkB pathway was surface topography dependent. The Smooth surface showed the highest level of activation followed by the Etched then the SLA. Addition of suboptimal concentrations of LPS mildly enhanced the response by signalling through the Toll receptor. Activation of NFKB occurred in the absence of fetal calf sera, although to a lesser extent. All three surfaces had very few cells with nuclear translocation at the 5 minutes time point with no significant statistical differences between the surfaces. After 30 minutes, translocation reached comparable levels to those surfaces tested with complete medium. Disruption of the lipid rafts affected the triggering and signalling of the NFkB pathway. This inhibitory effect was concentration and time dependent. Smooth surfaces bound more macrophages in the 30 minutes assay. Fetal calf serum appeared to be very critical for adhesion and spreading of the macrophages on the various surfaces examined. Removal of cholesterol did not affect adhesion or spreading on their respective surfaces. We have clearly demonstrated that the lipid rafts along with surface topography play a role in the activation on NFKB. This in-vitro study has demonstrated that surface topography modulated activation of the NFKB signalling pathway in a time-dependent manner. However, at present, it is unclear through which receptor(s) / surface structure the signal pathway is initiated.

The understanding of mechanical properties of thin films at the nano/sub micron level is important for rational selection of coatings for critical applications. In this thesis, the nanomechanical properties of plasma polymerised thin films were investigated in detail. The principal aim of the present work is to gain a fundamental understanding of the nanomechanical properties of plasma polymerised siloxane thin films, and the influence of the substrate on those properties. / Thesis (MApSc(MineralsandMaterials)--University of South Australia, 2006

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. / SAMs can form spontaneously onto a surface by immersing the substrate into an appropriate surfactant solution. They have been used, generally formed on gold surfaces, for biosensors, chemical sensors, micro-electronics and detection of DNA and protein adsorption. In our study, mercury was chosen as the substrate, for its defect-free, renewable and molecularly smooth surface. The additional advantage of being an ideal polarisable electrode allows a potential to be applied to the mercury, and hence control of the surface forces. The charging behaviour of the mercury is changed by introducing a SAM onto the surface. An uncharged SAM (11-mercapto-1-undecanol or 11-mercaptoundecane) modifies the dipole potential of the mercury by replacing the water molecules oriented on the surface, whereas a charge SAM (11-mecapto-1-undecanoic acid) brings additional charges to the surface. / Drop deformation is an important factor when deformable surfaces are involved in colloidal systems, e.g. emulsions, foams, in mineral flotation and in biological systems. Drop profiles of a mercury surface which is already close ( ̃50 nm) to a flat mica sheet, with or without a SAM, were measured using the SFA technique. For the SAM-modified mercury, the negatively charged functional group (-COO⁻) yields a repulsion against mica, and a thin film is formed between the surfaces. When the applied potential was scanned negatively, desorption of thiols occurred at certain potentials, increasing the local solute concentration in the solution. The restricted flow of the solute within the small gap creates an excess osmotic pressure in the thin film compared to the bulk solution. As a result, the film pressure exceeds the internal pressure of the drop, inverting the drop curvature and forming a dimple. We propose that the drainage of the dimple is a diffusion-controlled process, which is supported by the comparison of the data with a simple model calculation. / For the bare mercury drop, a negative potential was applied to the mercury to provide a repulsion to form a thin film. Mica was then driven towards the mercury with an abrupt step. Beyond certain step sizes, a rippled shape - which we dub a “wimple” - was observed before it evolved into a classical hydrodynamic dimple. At small step sizes, no wimple was observed, but curiously the film in the central part thickens before eventually thinning out. This shows that fluid first flows towards the central axis before reversing its flow direction and flowing radially outwards. / Thesis ([PhDApSc(MineralsandMaterials)])--University of South Australia, 2005.

The wettability of materials is important in many natural and industrial processes. In this thesis, the wettability of chemically heterogeneous surfaces was investigated with respect to the size, shape and orientation of individual defects. Heterogeneous surfaces were structured by photolithography, using self-assembled monolayers (SAMs) of diverse functionality and, thus, wettability. In order to maximise any possible departure from theory, the wettability of the high-and low-energy regions of these heterogenous surfaces was chosen to differ substantially. The purity of the defects was optimized by studying the SAM formation and the patterning processes, whilst the influence of roughness was minimized. The focus of this work is therefore on chemical heterogeneity. The Wilhelmy plate method was employed to ascertain the wetting behaviour of individual high- and low-energy defects. Simultaneous measurement of the capillary force and the plate position allowed full characterization of the wettability at the defect boundaries. In addition, integration of the Wilhelmy trace enabled the work associated with advancing or receding a liquid over these defects to be quantified. / The defect boundary orientation was of critical importance to the wetting behaviour. Wetting boundaries perpendicular to the liquid front did not result in any deviation from theoretical predictions. Wetting boundaries that were arranged parallel to the liquid front, however, caused contact line pinning which, in turn, caused contact angle hysteresis. Therefore these boundaries are directly responsible for the departure from wetting theory for heterogeneous surfaces (i.e. the Cassie Equation). These observations are consistent with earlier studies of wetting hysteresis by Johnson and Dettre (1964) and Neumann and Good (1972). Extending their work, this thesis examined the extent of wetting hysteresis at individual rectangular defects with respect to the defect dimensions. The nature of wetting hysteresis was studied quantitatively and, as a result, a simple model for hysteresis was proposed. This model predicts that, for a high-energy defect, the work associated with an advancing liquid will always be less than the theoretical value due to capillary rise within the effect. However, the work associated with a receding liquid will be equal to the theoretical prediction (the opposite is true for low-energy defects). The proposed model was validated for two different liquids (water and ethylene glycol) rectangular and circular defects of macroscopic dimensions. For these surfaces, the empirical data and the proposed model showed excellent agreement for both high- and low-energy defects. This agreement is strong evidence that high- and low-energy defects induce distinctly different wetting behaviour on heterogeneous surfaces. / The proposed model for hysteresis was qualitatively applied to heterogeneous surfaces containing micro- and nanoscopic defects. For micropatterns of high- and low-energy defects, of identical composition, the wettability was entirely different. High-energy defects induced a deviation from theory for only the advancing contact angles, whilst low-energy defects only influenced the receding angles. These observations were qualitatively consistent with the outcomes predicted by the proposed model for hysteresis. For nanoscopic defects, however, the advancing contact angles were consistent with Cassie's law within reasonable error. The derivation of Cassie's equation assumes that there is no capillary rise within the chemical defects. The capillary rise within a nanoscopic defect must be extremely small, according to extrapolation of measurements performed on macro and microscopic defects. Therefore, consistency between the wettability of nanoscopic defects and Cassie equation predictions might be expected. The hysteresis mechanism outlined within this thesis can be quantitatively applied to macroscopic defects, whereas its application to micro and nanoscopic defects is qualitative. / Finally, several applications of this fundamental research, which are directly related to real systems, have been outlined. These include mineral flotation, oil recovery, liquid movement, directed crystallization, Secondary Ion Mass Spectrometry for flotation analysis and patterning of inorganic surfaces. / Thesis (PhDApSc(MineralsandMaterials))--University of South Australia, 2004.

Thesis (PhD)--University of South Australia, 2004.

Thesis (PhD)--University of South Australia, 2003.

Thesis (PhDAppliedScience)--University of South Australia, 2002.

Thesis (PhD)--University of South Australia, 2000