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dc.contributor.advisorBlom, P.W.E.
dc.contributor.authorNgeleka, Tholakele Prisca
dc.date.accessioned2011-04-08T12:00:53Z
dc.date.available2011-04-08T12:00:53Z
dc.date.issued2008
dc.identifier.urihttp://hdl.handle.net/10394/4108
dc.descriptionThesis (M.Sc. (Nuclear Engineering))--North-West University, Potchefstroom Campus, 2009.
dc.description.abstractAn investigation was undertaken to determine the feasibility of increasing the hydrogen production rate by coupling the water gas shift (WGS) process to the hybrid sulphur process (HyS). This investigation also involved the technical and economical analysis of the water gas shift and the H2 separation by means of Pressure swing adsorption (PSA) process. A technical analysis of the water gas shift reaction was determined under the operating conditions selected on the basis of some information available in the literature. The high temperature system (HTS) and low temperature system (LTS) reactors were assumed to be operated at temperatures of 350°C and 200°C, respectively. The operating pressure for both reactors was assumed to be 30 atmospheres. The H2 production rate of the partial oxidation (POX) and the WGS processes was 242T/D, which is approximately two times the amount produced by the HyS process alone. The PSA was used for the purification process leading to a hydrogen product with a purity of 99.99%. From the total H2 produced by the POX and the WGS processes only 90 percent of H2 is recovered in the PSA. The unrecovered H2 leaves the PSA as a purge gas together with C02 and traces of CH4, CO, and saturated H20.
dc.publisherNorth-West University
dc.subjectPartial oxidation of methaneen
dc.subjectWater gas shift reactionen
dc.subjectIncreasing H₂ productionen
dc.subjectHigh and low temperatureen
dc.subjectReactor sizingen
dc.subjectEconomic analysisen
dc.subjectPressure swing adsorptionen
dc.titleAn investigation into the feasibility of applying the watergas shift process to increase hydrogen production rate of the hybrid sulphur processen
dc.typeThesisen
dc.description.thesistypeMasters


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