School of Chemistry - Theses
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ItemThe structure of the oxide/aqueous electrolyte interface( 1975)The structure of the oxide/aqueous electrolyte interface has been studied. The surface porosity of several oxides to ions is evaluated and the contribution of such porosity to the double layer properties determined by surface charge measurements. The oxides studied are B.D.H. precipitated silica, before and after heat treatment, rutile, goethite, hematite and amorphous ferric oxide. The surface porosity was evaluated using nitrogen adsorption for physical porosity, tritium exchange for surface hydration and dissolution for surface crystallinity. It is found that the surfaces of metal oxides may be divided into two categories; those that are porous to ions and those that are non-porous. Of those studied only the precipitated silica and the amorphous ferric oxide are porous. The porosity is probably due to an easily permeated layer of hydrolysed oxidic material. It does lead to exceptionally high surface charges. However the non-porous oxides also exhibit high surface charges so that while surface porosity may, in some cases, contribute to oxide double layer properties, it cannot be a general explanation of the high differential capacities observed. A site-binding model for non-porous oxide/aqueous electrolyte interfaces is introduced, in which it is proposed that the adsorbed counter ions form interfacial ion pairs with discrete charged surface groups. This model is used to calculate theoretical surface charge densities and potentials at the Outer Helmholtz Plane. The calculated values are consistent with experimental data for oxides provided a high value of the inner zone capacity is accepted. An explanation is provided for the difference between silica and most other oxides in terms of the dissociation constants of the surface groups.
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ItemInterfacial effects on aqueous sonochemistry and sonoluminescence( 1999-06)The dissolution of quantum sized CdS and MnO2 particles in water was conducted using 20 kHz ultrasound. CdS particles were found to dissolve chemically via an oxidation process while MnO2 particles dissolved via a reductive process. It was found that the dissolution of the colloids could be controlled via the addition of surface active chemicals to solution and by varying the saturation gas type. In the presence of Na2S or propan-2-ol and argon gas, the dissolution of CdS was inhibited, whereas the addition of alcohols (methanol, ethanol, propan-2-ol, butan-1-ol and pentan-1-ol) to the MnO2 system led to an increase in the amount of dissolution for a given time of sonication. This increase in dissolution was found to be dependent on the ability of the surface active radical scavenger to accumulate around the bubble interface during the cavitation process. Eventually, at higher alcohol concentration there was a plateau or a limiting value reached for the efficiency of colloid dissolution which was common for each alcohol. (For complete abstract open document)
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ItemInterfacial tension study and rheological characterisation of water-in-oil emulsion explosives( 2007)Highly concentrated emulsion explosives are complex colloidal systems that remain robust for very many years after production. In this work a poly-isobutyl succinic anhydride (PIBSA) derived emulsions have been studied to understand the extraordinary nature of the stability and flow of these emulsions. In this study a model sodium oleate emulsion system is developed to further confirmation of the nature emulsion explosives. Two PIBSA based emulsifiers were used to prepare the emulsions. The main emulsifier of interest was comprised of an amide, ester and imide head group attached to a PIBSA chain, the second was entirely comprised of an imide head group attached to a PIBSA chain. The pendant drop method was used to obtain dynamic interfacial tension measurements for an interface between of paraffin oil/PIBSA-imide and ammonium nitrate, and dodecane/sodium oleate and sodium nitrate. The IsoFit-WardTordai computer package that incorporated Langmuir, Frumkin, Reorientation and Aggregation adsorption isotherms was used to calculate diffusion coefficients for total time adsorption. Diffusion coefficients for short time adsorption with Langmuir and Frumkin isotherms were determined and long time adsorption with the Langmuir isotherm were calculated. All of the diffusion coefficients results suggested that direct diffusion controlled adsorption was not the mechanism these surface active agents employed, rather, the results suggested that an activation barrier controlled adsorption process dominated the kinetics of the interfacial adsorption. There is much evidence to suggest that rheological properties of highly concentrated emulsions have not been characterised correctly for some time. This is mainly due to wall depletion or wall slip effect phenomenon inherent to rheological investigations performed on smooth stainless steel surfaces. The effect of wall slip was eliminated through physical means by performing rheological investigations with a sand blasted cone and plate, and the use of the vane geometry as a rheomter. Another method to eliminate wall slip effects in steady shear for highly concentrated emulsions was formulated and established in this investigation. A two-stage Tikhonov regularisation procedure that converts steady shear data into rheological property functions has been developed. The two-stage method is able to obtain not only the shear-stress shear-rate function but also the slip velocity as a function of wall shear- stress. The method is such that it obtains the rheological functions over the maximum range of shear-rate covered by the data. The results obtained using the new method were compared to those obtained using the sand blasted cone and plate and vane geometry with good agreement being observed. Over a 17 month period, a PIBSA based emulsion was observed in order to determine if any dramatic rheological changes were taking place with time, the results obtained in both shear and dynamic analysis effectively concluded that the PIBSA emulsion explosive was extremely stable and the minor changes observed were within experimental uncertainty of the measurements. Various microscopy techniques were used to determine the droplet structure and size distribution within various emulsions. Optical microscopy, Qualitative Phase Imaging, Differential Interference Contrast imaging were employed, and it was found that the PIBSA and PIBSA-imide emulsions had a spherical shape rather than a hexagonal close packed structure that was previously assumed for these emulsion explosives. Images of the sodium oleate emulsion indicated that there were obvious destabilising mechanisms at work, affecting the longevity of the emulsion.