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The catalytic conversion of low chain length hydrocarbons to liquid fuels using ion exchange resin

Includes bibliographical references.

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Bibliographic Details
Main Author: Schumann, Werner Karl
Other Authors: O'Connor, Cyril T
Format: Thesis
Language:English
Published: Department of Mechanical Engineering 2016
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access_status_str Open Access
author Schumann, Werner Karl
author2 O'Connor, Cyril T
author_browse O'Connor, Cyril T
Schumann, Werner Karl
author_facet O'Connor, Cyril T
Schumann, Werner Karl
author_sort Schumann, Werner Karl
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/21419
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:52:31.972Z
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 Mechanical Engineering
publisherStr Department of Mechanical Engineering
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/21419 The catalytic conversion of low chain length hydrocarbons to liquid fuels using ion exchange resin Schumann, Werner Karl O'Connor, Cyril T Mechanical Engineering Includes bibliographical references. The use of ion exchange resins in the polymerization of a c 4 -mixture to liquid fuels has shown that the catalyst is highly active, deactivates at a slow rate and selectively produces mainly dimers. Macropore diffusion resistance strongly influences the overall rate of the reaction. An increase in liquid production rate is obtained with increasing macroporosity, increasing degree of functionalization and decreasing catalyst bead size. A minimum acid strength of pKA = -2.4 is required. The liquid production rate is increased by increasing the reaction temperature and weight hourly space velocity. Moreover, longer chain length product are obtained with increasing reaction temperature and at reaction conditions, which result in the complete conversion of monomers. Recycling liquid product reduces the liquid production and increases the production of trimer at the expense of dimer. At moderate reaction temperatures ion exchange resins are regenerable but the activity of the catalyst is destroyed at reaction temperatures greater than approximately 130°C. Deactivation occurs parallel to the main reaction and is due to cationic fouling. The liquid product obtained is highly branched. The R.O.N. of the -180°C fraction is approximately 97 and the cetane number of the +180°C fraction approximately 35. 2016-08-22T12:24:01Z 2016-08-22T12:24:01Z 1984 Master Thesis Masters MSc http://hdl.handle.net/11427/21419 eng application/pdf Department of Mechanical Engineering Faculty of Engineering and the Built Environment University of Cape Town
spellingShingle Mechanical Engineering
Schumann, Werner Karl
The catalytic conversion of low chain length hydrocarbons to liquid fuels using ion exchange resin
thesis_degree_str Master's
title The catalytic conversion of low chain length hydrocarbons to liquid fuels using ion exchange resin
title_full The catalytic conversion of low chain length hydrocarbons to liquid fuels using ion exchange resin
title_fullStr The catalytic conversion of low chain length hydrocarbons to liquid fuels using ion exchange resin
title_full_unstemmed The catalytic conversion of low chain length hydrocarbons to liquid fuels using ion exchange resin
title_short The catalytic conversion of low chain length hydrocarbons to liquid fuels using ion exchange resin
title_sort catalytic conversion of low chain length hydrocarbons to liquid fuels using ion exchange resin
topic Mechanical Engineering
url http://hdl.handle.net/11427/21419
work_keys_str_mv AT schumannwernerkarl thecatalyticconversionoflowchainlengthhydrocarbonstoliquidfuelsusingionexchangeresin
AT schumannwernerkarl catalyticconversionoflowchainlengthhydrocarbonstoliquidfuelsusingionexchangeresin