Thesis (Ph. D.)--West Virginia University, 2004. / Title from document title page. Document formatted into pages; contains xiv, 187 p. : ill. (some col.). Vita. Includes abstract. Includes bibliographical references (p. 181-186).

Thesis (M.S.)--West Virginia University, 2004. / Title from document title page. Document formatted into pages; contains xv, 99 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 85-86).

Thesis (Ph. D.)--University of Washington, 1999. / Vita. Includes bibliographical references (leaves 71-75).

Thesis (Ph. D.)--Virginia Polytechnic Institute and State University, 1993. / Vita. Abstract. Includes bibliographical references (leaves 205-214). Also available via the Internet.

Thesis (Ph. D.)--University of Alberta, 2010. / Title from pdf file main screen (viewed on June 18, 2010). A thesis submitted to the Faculty of Graduate Studies and Research in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Chemical Engineering, Department of Chemical and Materials Engineering, University of Alberta. Includes bibliographical references.

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

Thesis (Ph. D.)--University of Alberta, 2010. / Title from pdf file main screen (viewed on June 29, 2010). A thesis submitted to the Faculty of Graduate Studies and Research in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Bioresource and Food Engineering, Department of Agricultural, Food and Nutritional Science, University of Alberta. Includes bibliographical references.

Thesis (M.S.)--West Virginia University, 2006. / Title from document title page. Document formatted into pages; contains ix, 81 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 68-69).

Submitted in fulfillment of the academic requirements for the degree of Master of Engineering in Engineering, Durban University of Technology, Durban, South Africa, 2018. / Many separation processes in the chemical and petrochemical industries are energy intensive, and unfortunately, involve a range of solvents that are environmentally harmful and destructive. Alternative, sustainable separation techniques are desired to replace these conventional methods used in the separation of azeotropic as well as close-boiling mixtures, with the intention of reducing energy costs and adverse impact on the environment. In the present study, a new class of solvents called deep eutectic solvents (DESs) of Type III were investigated as alternatives to conventional solvents currently employed in separation processes. DESs are classified as ‘green’ solvents because of a range of favourable properties including lower cost, desirable solubility properties and reduced environmental impact (Abbott et al., 2003b; Smith et al., 2014). The infinite dilution activity coefficients (IDACs) values of 24 solutes – including alk-1-anes, alk-1-enes, alk-1-ynes, cycloalkanes, alkanols, alkylbenzenes, heterocyclics, esters, and ketones – were measured at 313.15, 323.15, 333.15 and 343.15 K by gas-liquid chromatography (GLC) in DESs. The four investigated DESs were as follows: 1) Tetramethylammonium chloride + Glycerol (DES1); 2) Tetramethylammonium chloride + Ethylene Glycerol (DES2); 3) Tetramethylammonium chloride + 1,6 Hexanediol (DES3); and 4) Tetrapropylammonium bromide + 1,6 Hexanediol (DES4). This work focused on the performance of DESs as extractive solvents for selected azeotropic and close-boiling binary mixtures. The two key performance criteria for these extractive solvents – selectivity and capacity – were determined from experimental infinite dilution activity coefficients (IDACs) of various solutes. The effect of solute molecular structure on IDAC values was investigated. Moreover, the effect of varying the hydrogen bond donors (HBDs) in DESs on IDAC values was examined. Partial excess molar enthalpies at infinite dilution were determined from the experimental IDAC data. Moreover, common industrial separation problems were selected to investigate DES potential to separate various mixtures by determining selectivity and capacity at infinite dilution. The results obtained in this study indicate that the use of a long carbon chain HBDs greatly decreases miscibility of DESs with organic solutes. For systems such as n-heptane - toluene, acetone - ethanol, cyclohexane - benzene and n-hexane - benzene systems, DES4 was the best solvent regarding the separation performance index. However, further investigation for DES4 by measurements of vapour-liquid equilibria (VLE) and liquid-liquid equilibria (LLE) data is suggested, as these data would provide additional pertinent information regarding the separation of such mixtures using DES4. The data produced from this study can be used to extend the applicability range of predictive models such as Universal Quasi- Chemical Functional Group Activity Coefficients (UNIFAC) and modified UNIFAC (Do) which are already incorporated in some chemical engineering process simulators. / M

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.