The effects SIBX/C10 (or C12) TTC mixtures on flotation response of pyrite, gold and uranium from Anglogold Ashanti’s No 2 Gold Plant feed were investigated. In batch flotation tests where TTC was dosed from aged 1% wt stock solutions, synergism was shown to occur in gold flotation at 25 mole percent C12 TTC and in uranium flotation at a similar dosage of C10 TTC. With commercial C12 TTC, 8 mole percent recorded the highest uranium and gold recoveries. The SIBX/C12 TTC mixture had a greater effect on gold than on uranium. When C12 mercaptan replaced the TTC in SIBX mixtures, rates and recoveries decreased at all levels. Kinetics and recovery with a mixture of 92 mole percent SIBX and 8 mole percent commercial C12 TTC gave a better flotation activity than obtained with SIBX alone. A combination of SIBX and an aged 1% wt solution of TTC lost activity when compared to that of SIBX and commercial TTC. This was attributed to the hydrolysis of TTC. Micro-probe analysis, back-scattered electron images, and EDS analysis showed that all the uranium recovered in flotation concentrates was associated with either pyrite, galena or a carbonaceous material (karogen). This was attributed to the flotation of the uranium oxide minerals brannerite and uraninite. Conditioning at pH values between 1.9-3.7 improved kinetics of gold, sulphur and uranium collection, but sulphur and uranium final recoveries were lower and gold final recovery was higher than the standard. In the presence of 0.001M cyanide, equivalent to 70g/t copper sulphate failed to activate pyrite at both pH 5.5 and pH 7.2. At a similar molar dosage lead nitrate did activate pyrite at pH 5.5 but not at pH 7.2. / Dissertation (MEng(Metallurgical))--University of Pretoria, 2005. / Materials Science and Metallurgical Engineering / unrestricted

The objectives of this project have been to characterise the biooxidation of an auriferous pyrite/arsenopyrite flotation concentrate, and to interpret laboratory batch and continuous pilot plant data in the light of the logistic model. Furthermore, the possibility of predicting continuous biooxidation plant performance from batch data was considered. The batch testing was carried out on five narrowly sized fractions of Fairview concentrate, as well as on the bulk concentrate. Extents of removal of iron, arsenic and sulphide-sulphur were described by the logistic equation and values of the kinetic parameters obtained. Maximum rates of removal of these components, predicted by the logistic parameters, correlated well with experimentally determined rates of removal obtained from the linear portions of the fractional removal versus time curves. Bibliography: pages 93-98.

Magister Scientiae (Medical Bioscience) - MSc(MBS) / Recently nanoparticles (NPs) have been introduced and used in combination with therapeutic approaches to develop nanotechnology-enabled medicine. These nanostructures allow for the exploitation of the physiochemical properties which may be beneficial in cancer treatment. The use of NPs in nanomedicine has proven successful in modern chemotherapeutics and has demonstrated promising potential in in vivo and in vitro radiosensitization studies. This is a baseline study aimed to determine the cytotoxic effects of AuNPs for potential radiosensitization analysis. The study analysed the effects of different AuNP sizes (30, 50 and 80nm), concentrations (5, 10 and 15 μg/ml) over various time periods in CHOK1 and A549 cells. AuNPs were characterised by DLS and ZP analysis and showed that particles were moderately polydispersed and moderately to highly stable in charge. The effects on viability and metabolic activity of cells were determined using crystal violet and the WST-1 assay.

Removing pyrite from coal and pyrrhotite from pentlandite play a critical role in coal and nickel production, respectively, to meet the stringent restriction on SO2 emission. The present project investigates first the mechanism of xanthate adsorption on gold using Atomic Force Microscope (AFM), then the depression of pyrite and pyrrhotite using the synthetic polymers developed by Cytec Industries. The results show that for xanthate/gold system, dixanthogen is the only species that renders the surface hydrophobic. Chemisorbed xanthate is observed on the gold surface but is hydrophilic. The synthetic polymers may adsorb on pyrite and pyrrhotite possibly through the hydrophobic interaction between the hydrophobic moiety of the polymer and the mineral surface that has been hydrophobized by collector adsorption. The hydrophilic moieties of the polymer are exposed to the aqueous phase and render the surface hydrophilic. / Master of Science

Electrolyte interactions with colloidal nanoparticles (NPs) in aqueous solutions have been implicated in a wide range of research and applications. Existing studies on electrolyte interactions with NPs are primarily based on the electrical double layer (EDL) theory. However, the EDL model provides very limited information on how electrolytes directly bind to NPs, electrolyte impact on charge distribution on NPs, and NP morphological modification upon electrolyte binding. Furthermore, the previous reports have mainly focused on either cations or anions binding onto NPs, while the potential cation and anion coadsorption onto NPs and NPacilitated cation-anion interactions remain largely uncharted. Filling these knowledge gaps are critical to enhance the fundamental understanding of interfacial interactions of electrolytes with NPs. Experimental characterization of cations and anions at the solid/liquid interface is a challenging analytical task. In the first study, we demonstrated the first direct experimental evidence of ion pairing on gold nanoparticles (AuNPs) in water by using surface enhanced Raman spectroscopy (SERS) in combination with electrolyte washing. Unlike ion pairing in aqueous solutions where the oppositely charged ions are either in direct contact or separated by a solvation shell, the ion pairing on AuNPs refers to cation and anion coadsorption onto the same NP surface regardless of separation distance. Ion pairing reduces the electrolyte threshold concentration in inducing AuNP aggregation and enhances the competitiveness of electrolyte over neutral molecules in binding to AuNPs. In the second study, we demonstrated that binding, structure, and properties of an ionic species on AuNPs are significantly dependent on the counterion adsorbed on AuNPs. These counterion effects include electrolyte-induced AuNP aggregation and fusion, quantitative cation and anion coadsorption on AuNPs, and SERS spectral distortion induced by the ionic species on AuNP surfaces. In the final study, we proposed that ion pairing as the main mechanism for reducing electrostatic repulsion among organothiolates self-assembled on AuNPs in water by using a series of experimental and computational studies. The work described in this dissertation provides a series of new insights into electrolyte interfacial interactions with AuNPs.

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Gold nanoparticles (AuNPs) have been of interest due to their biocompatibility and surface plasmon resonance. Biomolecules can spontaneously adsorb to their surface, a trait that could be exploited for drug targeting. It is unclear, however, whether protein-AuNP interactions at the nanoparticle surface are dependent on nanoparticle size. In this project, we investigate whether surface curvature can induce protein unfolding and multilayer binding in citrate-coated AuNPs of various sizes. An NMR-based approach was utilized to determine the adsorption capacity, and protein NMR spectra were compared to determine whether nanoparticle size influences protein interactions. Transmission electron microscopy (TEM) was used to support the results. Over a range of AuNP sizes (15-100 nm) proteins appear globular on the nanoparticle surface. Additionally, a single layer of proteins is adsorbed regardless of AuNP size. Our results are consistent for two differently sized proteins, GB3 (6 kDa) and bovine carbonic anhydrase (BCA, 29 kDa).

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