Thesis (B.S.)--University of Missouri, School of Mines and Metallurgy, 1905. / Alfred A. Thomas determined to be Alfred Augustus Thomas from "Thirty-Ninth Annual Catalogue. School from Mines and Metallurgy. University of Missouri". The entire thesis text is included in file. Typescript. Illustrated by authors. Title from title screen of thesis/dissertation PDF file (viewed November 22, 2008)

Thesis (Professional Degree)--University of Missouri, School of Mines and Metallurgy, 1917. / The entire thesis text is included in file. Typescript. Illustrated by author. Title from title screen of thesis/dissertation PDF file (viewed May 11, 2009)

Thesis (B.S.)--University of Missouri, School of Mines and Metallurgy, 1904. / The entire thesis text is included in file. Typescript. Illustrated by authors. Title from title screen of thesis/dissertation PDF file (viewed January 23, 2009)

Thesis (M.S.)--West Virginia University, 1999. / Title from document title page. Document formatted into pages; contains xiii, 131 p. : ill. (some col.). Vita. Includes abstract. Includes bibliographical references (p. 61-64).

Thesis (Ph.D.(Materials Science & Metallurgical Engineering))--University of Pretoria, 2009. / Abstract in English. Includes bibliographical references.

Thesis (Ph.D.) - University of Queensland, 2004. / Includes bibliography.

Thesis (M. Sc.)(Chemistry)--University of Pretoria, 2003. / Title from opening screen (viewed March 22, 2006). Summaries in English and Afrikaans. Includes bibliographical references.

Thesis (MTech (Chemical Engineering))--Cape Peninsula University of Technology, 2016. / Nickel, a valuable base metal, is the predominant product from the Nkomati mine in South Africa. High-grade nickel mineral ores (2%) from the Massive Sulphide Body have been depleted leaving those of low grade (0.3%). The beneficiation of this ore presents a challenge to the minerals processing industry. In response, batch froth flotation tests were used to explore the effects of mixtures of potassium amyl xanthate (PAX) and IPETC (Isopropyl ethyl thionocarbamate) on the grades and recoveries of nickel. In the mixtures, the xanthate accounted for 95.5, 90, 85 and 80 mole% respectively. Generally an increase in the nickel grade and recovery was observed with the mixtures relative to PAX. IPETC gave a significant increase in the cumulative water recovery with a significant decrease in cumulative nickel grade relative to PAX. PAX gave the highest cumulative nickel grade for the singular collector tests (1.9%), while obtaining the lowest cumulative recovery (77%). Out of the collector mixtures, mixtures 85% PAX: 15% IPETC and 90% PAX: 10% IPETC produced the joint highest cumulative grades (1.8%). These mixtures both gave recoveries of 82%. Collector mixture 95.5% PAX: 4.5% IPETC gave the second highest grade (1.7%) and the highest nickel recovery (85%). Although there were differences in the cumulative nickel grades and recoveries there were statistically no significant improvements observed with the use of the mixtures of PAX and IPETC in comparison to the industry mixture (95.5% SIBX: 4.5% IPETC). Tests were performed using the three best performing collector mixtures at molar dosages of 1.3, 0.65 and 0.325mmol/t. The highest cumulative nickel grades were obtained at the lowest collector dosages (at a molar dosage of 0.325mmol/t of 95.5% SIBX: 4.5% IPETC) with collector mixture 95.5% PAX: 4.5% IPETC being the most selective with a nickel grade of 2%. It was also observed that an increase in collector dosage, generally increased the cumulative nickel recovery with collector mixture 95.5% PAX: 4.5% IPETC at a molar dosage of 1.3mmol/t gave the highest cumulative recovery out of the tested mixtures (85%). The study also indicated that an increase in selectivity (i.e. cumulative grade) was at the expense of cumulative recovery. With a decrease in dosage, there was no significant improvement in the cumulative nickel grade and recovery for the tested mixtures compared to the industry mixture. There was however a significant decrease in the water recoveries achieved with PAX and collector mixtures 95.5% PAX: 4.5% IPETC at a molar dosage of 1.3mmolg/t of as well as mixture 90% PAX: 10% IPETC at a molar dosage of 0.65mmol/t.

Complications during the healing process of skin wounds often arise due to infection by pathogenic bacteria. Bacterial hydrolytic enzymes degrade the host tissue while biofilms can shield the bacterial cells from the host's immune response. Wound dressings with bacteriostatic or bactericidal properties are a promising solution. This study investigated the potential of surface acetylated bacterial cellulose as a novel antibacterial wound dressing. Hydroxyl groups on the surface of bacterial cellulose were substituted with acetyl groups using acetic anhydride in a citric acid-catalyzed reaction. The resulting ester linkages between the acetyl groups and bacterial cellulose surface were hypothesized to be cleaved by bacterial esterases or other hydrolytic enzymes such that acetic acid, a well-known antibacterial compound, will be produced leading to the death of the bacterial cells. Surface acetylation was confirmed via FTIR and its effect on the morphology of bacterial cellulose was analyzed with FESEM and XRD while the degree of substitution was determined by HPLC-UV. Indirect contact human cell cytotoxicity assays using extracts from surface acetylated bacterial cellulose showed no cytotoxic effect on human umbilical vein endothelial cells. Two types of antibacterial assays were performed in which surface acetylated bacterial cellulose was exposed to Staphylococcus epidermidis, Escherichia coli, and Pseudomonas aeruginosa which were selected as model bacteria for Gram-positive, Gram-negative, and pathogenic bacterial species, respectively. Neither assay showed a reduction of bacterial cell viability. Further research is needed to determine if the acetyl ester linkages on the surface of bacterial cellulose are susceptible to cleavage by bacterial esterase enzymes. / Master of Science / The healing of skin wounds is frequently complicated by infection of the wound with harmful bacteria. A potential remedy could be wound dressings that kill such bacteria. Bacterial cellulose is a naturally occurring biomaterial with multiple properties that make it an ideal material for wound dressings. Pure bacterial cellulose has no inherent antibacterial properties but can be chemically modified with a separate substance that is antibacterial such as acetic acid. This study investigates the potential of chemically modified bacterial cellulose in antibacterial wound dressing applications. The material may release acetic acid in the presence of bacteria and cause cell death. A series of human cell and antibacterial assays were carried out to test the ability of the modified bacterial cellulose to inhibit bacterial growth as well as any potential harmful effect on human cells. While it showed no adverse effects on human cells, the modified bacterial cellulose did not reduce bacterial cell viability.

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