Thesis (M.Ing. (Chemical Engineering))--North-West University, Potchefstroom Campus, 2009.

Catalytic supercritical water gasification (SCWG) is a promising technology for hydrogen and methane production from wet organic feedstocks at relatively low temperatures (e.g. <500 oC). However, in order to make this process technically and economically viable, solid catalyst with enhanced activity and improved hydrogen selectivity should be developed. In this study, different aspects of catalytic SCWG have been investigated. The performance of several supported-nickel catalysts were examined to identify catalysts that lead to high carbon conversion and high hydrogen yields under near-critical conditions (i.e. near 374 oC). Moreover, for the first time, the effects of several parameters which dominated the activity of the supported nickel catalysts have been systematically investigated. Among the several different catalyst supports evaluated at 5% nickel loading, α-Al2O3, carbon nanotube (CNT), and MgO supports resulted in highest carbon conversions, while SiO2, Y2O3, hydrotalcite, yttria-stabilized zirconia (YSZ), and TiO2 showed modest activities. Comparing the XRD patterns for the support materials before and after the exposure to supercritical water, α-Al2O3, YSZ, and TiO2 were found to be hydrothermally stable among the metal oxide supports. Using the same amount of nickel on α-Al2O3, the methane yield decreased by increasing the nickel to support ratio whereas the carbon conversion was only slightly affected. At a given nickel to support ratio, a threefold increase in methane yield was observed by increasing the temperature from 350 to 410 oC. The catalytic activity also increased by the addition small quantity of potassium. The activity of Ni/γ-Al2O3 catalyst varied based on the affinity of the catalyst to form nickel aluminate spinel. This is also the first report on the role of oxidative pretreatment of the carbon nanotubes by nitric acid on the performance of these catalysts for the supercritical water gasification process. Using different lignocellulosic feeds, it was found that the gasification of glucose, fructose, cellulose, xylan and pulp resulted in comparable gas yields (± 10%) after 60 min, whereas alkali lignin was substantially harder to gasify. Interestingly, gasification yield of bark, which had a high lignin content, was comparable to those of cellulose. In summary, the Ni/α-Al2O3 catalyst had a higher hydrogen selectivity and comparable catalytic activity to the best commercially available catalysts for SCWG of carbohydrates.

Gasification technologies are expected to play a key role in the future of solid waste management since the conversion of municipal and industrial solid wastes to a gaseous fuel significantly increases its value. Municipal solid waste (MSW) gasification for electrical power generation was conducted in a fluidized bed gasifier and the feasibility of using a control system was evaluated to facilitate its management and operation. The performance of an engine using the gas produced was evaluated. A procedure was also tested to upgrade the quality of the gas and optimize its production. The devices installed and automated control system developed was able to achieve and maintain the set conditions for optimum gasification. The most important parameters of reaction temperature and equivalence ratio were fully controlled. Gas production went at a rate of 4.00 kg min-1 with a yield of 2.78 m3 kg-1 of fuel and a heating value (HV) of 7.94 MJ Nm-3. Within the set limits of the tests, the highest production of synthesis gas and the net heating value of 8.97 MJ Nm-3 resulted from gasification at 725°C and ER of 0.25 which was very close to the predicted value of 7.47 MJ Nm-3. This was not affected by temperature but significantly affected by the equivalence ratio. The overall engine-generator efficiency at 7.5 kW electrical power load was lower at 19.81% for gasoline fueled engine compared to 35.27% for synthesis gas. The pressure swing adsorption (PSA) system increased the net heating value of the product gas by an average of 38% gas over that of inlet gas. There were no traces of carbon dioxide in the product gas indicating that it had been completely adsorbed by the system. MSW showed relatively lower fouling and slagging tendencies than cotton gin trash (CGT) and dairy manure (DM). This was further supported by the compressive strength measurements of the ash of MSW, CGT and DM and the EDS elemental analysis of the MSW ash.

Thesis (M. Eng.(Industrial Engineering))-Universiteit van Pretoria, 2007. / Abstract in English. Includes bibliographical references.

Thesis (Ph. D.)--University of Adelaide, Dept. of Chemical Engineering, 1999. / Includes bibliographical references (leaves 322-335).

Thesis (M.S.)--West Virginia University, 2008. / Title from document title page. Document formatted into pages; contains x, 67 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 63-67).

Thesis (M. Sc.)--University of Alberta, 2009. / Title from pdf file main screen (viewed on July 10, 2009). "A thesis submitted to the Faculty of Graduate Studies and Research in partial fulfillment of the requirements for the degree of Master of Science, Department of Mechanical Engineering, University of Alberta." Includes bibliographical references.

Thesis (M.S.)--University of Alabama at Birmingham, 2006. / Description based on contents viewed Jan. 29, 2007; title from title screen. Includes bibliographical references (p. 42-44).

Thesis (Ph.D.) - University of Queensland, 2006. / Includes bibliography.

Thesis (M.E.)--University of Canterbury, 2006. / Typescript (photocopy). Includes bibliographical references (p. 108-112). Also available via the World Wide Web.