No description available.

No description available.

A high resolution capillary gas chromatography technique has been adapted to the analysis of polydisperse non-ionic surfactants. This technique has enabled the complete characterization of the oligomer distributions of very small samples of surfactants (typically 0.1 µg to 0.5 µg). It has made possible the determination of changes in the oligomer distribution on adsorption of surfactant at the solid/aqueous interface. Isotherms have been measured for the adsorption of a series of polyoxyethylene nonylphenol surfactants from aqueous solution on to various solids. These isotherms indicate that the surfactant – surface interaction increases with an increase in the hydrophobicity of the adsorbent. They also show a dependence upon the average length of the ethylene oxide chain and the ratio of the surface area/solution volume. These latter factors affect both the total partition of surfactant between the surface and the solution, and also the selectivity of the solid surface. A detailed study of the adsorption of N8 (a commercial non-ionic surfactant) by a precipitated silica at various surface area/solution ratios, has been undertaken, where the equilibrium surfactant oligomer distributions in the adsorbed and solution phases have been determined. At surfactant concentrations above the critical micelle concentration, the phase separation approach has been used to estimate the surfactant oligomer distributions in free monomer solution and in micelles. This information has been combined with a surface phase model to interpret the results of the adsorption distribution studies.

No description available.

Surface spectroscopic techniques have been applied to facets of the flotation beneficiation and hydrometallurgical extraction of sulfide minerals to enhance the fundamental understanding of these industrially important processes. As a precursor to the determination of surface chemical composition, the sub-surface properties of some sulfide minerals that have not previously been fully characterised were also investigated. The electronic properties of ??-NiS and ??-NiS (millerite), Ni3S2 (heazlewoodite), (Ni,Fe)9S8 (pentlandite), CuFe2S3 (cubanite), CuFeS2 (chalcopyrite), Cu5FeS4 (bornite) and CuS (covellite) were investigated by conventional and synchrotron X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy augmented by ab initio density of state calculations and NEXAFS spectral simulations. Particular aspects studied included the relationship between sulfur coordination number and core electron binding energies, the higher than expected core electron binding energies for the sulfur in the metal-excess nickel sulfides, and the formal oxidation states of the Cu and Fe in Cu-Fe sulfides. It was concluded that the binding energy dependence on coordination number was less than previously believed, that Ni-Ni bonding was the most likely explanation for the unusual properties of the Ni sulfides, and that there was no convincing evidence for Cu(II) in sulfides as had been claimed. Most of the NEXAFS spectra simulated by the FEFF8 and WIEN2k ab initio codes agreed well with experimental spectra, and the calculated densities of states were useful in rationalising the observed properties. XPS, static secondary ion mass spectrometry (SIMS) and NEXAFS spectroscopy were used to investigate thiol flotation collector adsorption on several sulfides in order to determine the way in which the collector chemisorbs to the mineral surface, to differentiate monolayer from multilayer coverage, and to characterise the multilayer species. It was found that static SIMS alone was able to differentiate monolayer from multilayer coverage, and together with angle-resolved NEXAFS spectroscopy, was also able to confirm that 2-mercaptobenzothiazole interacted through both its N and exocyclic S atoms. The altered layers formed on chalcopyrite and heazlewoodite during acid leaching were examined primarily by means of threshold S KLL Auger electron spectroscopy, but no evidence for buried interfacial species was obtained.

Surface spectroscopic techniques have been applied to facets of the flotation beneficiation and hydrometallurgical extraction of sulfide minerals to enhance the fundamental understanding of these industrially important processes. As a precursor to the determination of surface chemical composition, the sub-surface properties of some sulfide minerals that have not previously been fully characterised were also investigated. The electronic properties of ??-NiS and ??-NiS (millerite), Ni3S2 (heazlewoodite), (Ni,Fe)9S8 (pentlandite), CuFe2S3 (cubanite), CuFeS2 (chalcopyrite), Cu5FeS4 (bornite) and CuS (covellite) were investigated by conventional and synchrotron X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy augmented by ab initio density of state calculations and NEXAFS spectral simulations. Particular aspects studied included the relationship between sulfur coordination number and core electron binding energies, the higher than expected core electron binding energies for the sulfur in the metal-excess nickel sulfides, and the formal oxidation states of the Cu and Fe in Cu-Fe sulfides. It was concluded that the binding energy dependence on coordination number was less than previously believed, that Ni-Ni bonding was the most likely explanation for the unusual properties of the Ni sulfides, and that there was no convincing evidence for Cu(II) in sulfides as had been claimed. Most of the NEXAFS spectra simulated by the FEFF8 and WIEN2k ab initio codes agreed well with experimental spectra, and the calculated densities of states were useful in rationalising the observed properties. XPS, static secondary ion mass spectrometry (SIMS) and NEXAFS spectroscopy were used to investigate thiol flotation collector adsorption on several sulfides in order to determine the way in which the collector chemisorbs to the mineral surface, to differentiate monolayer from multilayer coverage, and to characterise the multilayer species. It was found that static SIMS alone was able to differentiate monolayer from multilayer coverage, and together with angle-resolved NEXAFS spectroscopy, was also able to confirm that 2-mercaptobenzothiazole interacted through both its N and exocyclic S atoms. The altered layers formed on chalcopyrite and heazlewoodite during acid leaching were examined primarily by means of threshold S KLL Auger electron spectroscopy, but no evidence for buried interfacial species was obtained.

The DC casting process used for the production of cast aluminium alloy products intended for processing by rolling, extrusion or forging is an economically important process with approximately 10 million tonnes of DC cast product being produced annually world wide [1]. Process productivity, particularly with respect to elimination of casting defects and hence process scrap is an important factor to DC cast product producers. The literature reporting the DC casting process, particularly with respect to the formation of defects on the cast surface, is reviewed and the mechanisms for the formation of such defects examined. A universally understood and accepted explanation was found for only one of the normal surface defects encountered in practice. A number of samples of commercially cast DC products were subject to detailed cast surface examination, particularly surface microstructures. The results of this examination and the literature survey identified molten metal surface tension as a possible contributing factor affecting the molten metal meniscus stability within the DC casting mould. Meniscus instability is linked with the formation of surface defects. The literature on surface tension of aluminium alloys provided only limited information hence the surface tension of a range of binary and ternary alloys, including commercial alloys was determined, producing data hitherto not available. Of the common alloying elements used in commercial aluminium alloys, iron and magnesium were found to significantly reduce the surface tension. Surface fracture also resulted in a reduction in surface tension for the majority of alloys tested. The surface tension data is combined with mould thermal and physical model calculations to propose a mechanism for the formation of the cast surface defects. The model proposes a maximum stable size for the meniscus according to the alloy and mould conditions. Conditions outside these limits result in meniscus instability and the formation of cast surface defects. The model suggests possible operating changes that may reduce the incidence of surface defect formation. The work also identifies a number of areas requiring further investigation before major practical process changes aimed at cast surface defect elimination, may be formulated.

Thesis (Ph. D.)--University of Texas at Austin, 2007. / Vita. Includes bibliographical references.

Thesis (Ph. D.)--McMaster University (Canada), 1988. / Source: Dissertation Abstracts International, Volume: 49-11, Section: B, page: 4838. Supervisor: Michael L. Klein.

Diss. (sammanfattning) Luleå : Luleå tekniska univ., 2004. / Härtill 5 uppsatser.