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Gas-solid chromatographic studies of two well-known catalysts

Bibliography:pages 116-120.

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Main Author: Mason, Robert Peter
Other Authors: Irving, H M N H
Format: Thesis
Language:English
Published: Department of Chemistry 2016
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access_status_str Open Access
author Mason, Robert Peter
author2 Irving, H M N H
author_browse Irving, H M N H
Mason, Robert Peter
author_facet Irving, H M N H
Mason, Robert Peter
author_sort Mason, Robert Peter
collection Thesis
description Bibliography:pages 116-120.
format Thesis
id oai:open.uct.ac.za:11427/22190
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:50:44.225Z
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 Chemistry
publisherStr Department of Chemistry
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source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/22190 Gas-solid chromatographic studies of two well-known catalysts Mason, Robert Peter Irving, H M N H Koch, Klaus R Chemistry Bibliography:pages 116-120. This work was initiated to explore the scope and feasibility of using a gas chromatograph to study catalytic reactions. Various methods have been proposed in the literature and it was decided to investigate various possible systems. Two catalysts were chosen for study. The dehydration of alcohols over alumina catalysts has been extensively studied and found to be ideally suited to studies by gas chromatography. The effect of modification of the catalyst by inorganic ions and by water was investigated. The dehydration of ethanol and pentanol were studied. Results indicated that alumina has two types of active sites responsible for the dehydration of alcohols. Zeolite catalysts are well-known and in this work the catalytic cracking of alkanes over zeolite Y was studied. The reaction mechanism was found to be complex and catalyst deactivation due to build-up of highly carbonaceous deposits occurred. All components of the reaction products were produced at similar rates to the overall reaction rate indicating that desorption of alkane product species was not the rate determining step. Between 150° and 300°C propane was the smallest product formed. Only alkanes were found in the product spectrum which was temperature dependent. Addition of hydrogen gas greatly increased the amount of detectable products. Heptane was found to react significantly above 200 °C, hexane about above 225°C and pentane above 250°C. Hexane and cyclohexane reacted at similar temperatures. 2016-10-19T03:58:03Z 2016-10-19T03:58:03Z 1983 Master Thesis Masters MSc http://hdl.handle.net/11427/22190 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
Mason, Robert Peter
Gas-solid chromatographic studies of two well-known catalysts
thesis_degree_str Master's
title Gas-solid chromatographic studies of two well-known catalysts
title_full Gas-solid chromatographic studies of two well-known catalysts
title_fullStr Gas-solid chromatographic studies of two well-known catalysts
title_full_unstemmed Gas-solid chromatographic studies of two well-known catalysts
title_short Gas-solid chromatographic studies of two well-known catalysts
title_sort gas solid chromatographic studies of two well known catalysts
topic Chemistry
url http://hdl.handle.net/11427/22190
work_keys_str_mv AT masonrobertpeter gassolidchromatographicstudiesoftwowellknowncatalysts