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The preferential oxidation (PrOx) activity of two Ru/Al2O3 catalysts prepared using different methods was tested. The first catalyst was prepared by wetness impregnation at a high pH and the second was prepared by incipient wetness impregnation. Catalytic activity was measured at varying temperature...
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| Format: | Thesis |
| Language: | English |
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Department of Chemical Engineering
2016
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| _version_ | 1867613245979754496 |
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| access_status_str | Open Access |
| author | Muziki, Sibongile |
| author2 | Fletcher, Jack |
| author_browse | Fletcher, Jack Muziki, Sibongile |
| author_facet | Fletcher, Jack Muziki, Sibongile |
| author_sort | Muziki, Sibongile |
| collection | Thesis |
| description | The preferential oxidation (PrOx) activity of two Ru/Al2O3 catalysts prepared using different methods was tested. The first catalyst was prepared by wetness impregnation at a high pH and the second was prepared by incipient wetness impregnation. Catalytic activity was measured at varying temperatures, space velocities as well as O2/CO ratio. The Ru catalyst catalyst prepared using wetness impregnation at high pH was found to exhibit higher CO conversion despite having a lower Ru dispersion compared to the Ru catalyst prepared using incipient wetness impregnation at the tested temperature range. For both Ru catalysts the trends observed with varying temperature, space velocity as well as O2/CO ratio were similar. Increasing temperature increased CO conversion up to a maximum after which a further increase in temperature led to a decrease in CO conversion. At low temperatures, increasing space velocity resulted in a decrease in CO conversion. An increase in CO conversion was observed with increasing space velocity at higher temperatures. Increasing space velocity led to a decrease in CH4 formation at high temperatures. Furthermore it was determined that mass transfer limitations played a role during the catalytic process. The effects of mass transfer limitations could be reduced by increase the linear space velocity. A Pt-Fe/mordenite catalyst was prepared in this study using solid state ion exchange to deposit Fe and competitive ion exchange to deposit Pt. This method was proposed in order to try and improve the preparation method reported in literature. The synthesised catalyst did not perform as well as the Pt-Fe/Mordenite reported in literature. A maximum CO conversion of 99 % with 47 % CO2 selectivity at 180 °C, 120 000 ml/(h gcat) and O2/CO ratio of 1 was achieved. |
| format | Thesis |
| id | oai:open.uct.ac.za:11427/20090 |
| institution | University of Cape Town (South Africa) |
| language | eng |
| last_indexed | 2026-06-10T12:33:05.164Z |
| license_str | Not specified — see source repository |
| provenance_str_mv | Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository |
| publishDate | 2016 |
| publishDateRange | 2016 |
| publishDateSort | 2016 |
| publisher | Department of Chemical Engineering |
| publisherStr | Department of Chemical Engineering |
| record_format | dspace |
| source_str | UCTD — University of Cape Town Open Access Repository |
| spelling | oai:open.uct.ac.za:11427/20090 Carbon monoxide clean-up of reformate gas by preferential oxidation Muziki, Sibongile Fletcher, Jack Brosius, Roald Chemical Engineering The preferential oxidation (PrOx) activity of two Ru/Al2O3 catalysts prepared using different methods was tested. The first catalyst was prepared by wetness impregnation at a high pH and the second was prepared by incipient wetness impregnation. Catalytic activity was measured at varying temperatures, space velocities as well as O2/CO ratio. The Ru catalyst catalyst prepared using wetness impregnation at high pH was found to exhibit higher CO conversion despite having a lower Ru dispersion compared to the Ru catalyst prepared using incipient wetness impregnation at the tested temperature range. For both Ru catalysts the trends observed with varying temperature, space velocity as well as O2/CO ratio were similar. Increasing temperature increased CO conversion up to a maximum after which a further increase in temperature led to a decrease in CO conversion. At low temperatures, increasing space velocity resulted in a decrease in CO conversion. An increase in CO conversion was observed with increasing space velocity at higher temperatures. Increasing space velocity led to a decrease in CH4 formation at high temperatures. Furthermore it was determined that mass transfer limitations played a role during the catalytic process. The effects of mass transfer limitations could be reduced by increase the linear space velocity. A Pt-Fe/mordenite catalyst was prepared in this study using solid state ion exchange to deposit Fe and competitive ion exchange to deposit Pt. This method was proposed in order to try and improve the preparation method reported in literature. The synthesised catalyst did not perform as well as the Pt-Fe/Mordenite reported in literature. A maximum CO conversion of 99 % with 47 % CO2 selectivity at 180 °C, 120 000 ml/(h gcat) and O2/CO ratio of 1 was achieved. 2016-06-22T08:58:00Z 2016-06-22T08:58:00Z 2015 Master Thesis Masters MSc (Eng) http://hdl.handle.net/11427/20090 eng application/pdf Department of Chemical Engineering Faculty of Engineering and the Built Environment University of Cape Town |
| spellingShingle | Chemical Engineering Muziki, Sibongile Carbon monoxide clean-up of reformate gas by preferential oxidation |
| thesis_degree_str | Master's |
| title | Carbon monoxide clean-up of reformate gas by preferential oxidation |
| title_full | Carbon monoxide clean-up of reformate gas by preferential oxidation |
| title_fullStr | Carbon monoxide clean-up of reformate gas by preferential oxidation |
| title_full_unstemmed | Carbon monoxide clean-up of reformate gas by preferential oxidation |
| title_short | Carbon monoxide clean-up of reformate gas by preferential oxidation |
| title_sort | carbon monoxide clean up of reformate gas by preferential oxidation |
| topic | Chemical Engineering |
| url | http://hdl.handle.net/11427/20090 |
| work_keys_str_mv | AT muzikisibongile carbonmonoxidecleanupofreformategasbypreferentialoxidation |