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Alkylation of phenol with methanol over H-ZSM-5, H-Beta, H-Mordenite, H-USY and H-MCM-22

Bibliography: leaves 223-232.

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Bibliographic Details
Main Author: Moon, Gillian Catherine
Other Authors: O'Connor, Cyril
Format: Thesis
Language:English
Published: Department of Mechanical Engineering 2014
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access_status_str Open Access
author Moon, Gillian Catherine
author2 O'Connor, Cyril
author_browse Moon, Gillian Catherine
O'Connor, Cyril
author_facet O'Connor, Cyril
Moon, Gillian Catherine
author_sort Moon, Gillian Catherine
collection Thesis
description Bibliography: leaves 223-232.
format Thesis
id oai:open.uct.ac.za:11427/8595
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:33.381Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
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:11427/8595 Alkylation of phenol with methanol over H-ZSM-5, H-Beta, H-Mordenite, H-USY and H-MCM-22 Moon, Gillian Catherine O'Connor, Cyril Möller, Klaus Chemical Engineering Bibliography: leaves 223-232. Alkylphenols are intermediates used in the synthesis of many important substances. The most significant of the commercially important lower alkylphenols are cresols (methyl phenols) and xylenols (dimethyl phenols). The main markets for alkylphenol products are nonionic detergents, phenolic resins, polymer additives and agrochemicals. Of the western world cresol market, 55% originates from synthetic cresols whereas 45% originates from so-called “natural” cresols obtained from coal tars and refinery caustics. The methylation of phenol is the only process specifically developed to produce cresols and xylenols. There are three cresol isomers, namely ortho, para and meta. It is possible to produce a high selectivity to o-cresol by alkylation of phenol with methanol over a basic or a Al2O3 catalyst or a Fe/V catalyst. A mixture of the cresol isomers can be obtained over aluminium oxides with strong acid sites, silica alumina, zeolites, aluminium phosphates and phosphoric acid-Kieselguhr catalysts. However, direct synthesis of high purity m-cresol and p-cresol is desirable due to the high costs of separating these two isomers. Thus to synthesize p-cresol, a m-cresol free or very low m-cresol concentration in the product is desirable for purification reasons and a high p/o-cresol ratio is also desirable in the product for yield reasons since separation of the p- and the o-cresols is economically possible. 2014-10-18T05:57:51Z 2014-10-18T05:57:51Z 2003 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/8595 eng application/pdf Department of Mechanical Engineering Faculty of Engineering and the Built Environment University of Cape Town
spellingShingle Chemical Engineering
Moon, Gillian Catherine
Alkylation of phenol with methanol over H-ZSM-5, H-Beta, H-Mordenite, H-USY and H-MCM-22
thesis_degree_str Doctoral
title Alkylation of phenol with methanol over H-ZSM-5, H-Beta, H-Mordenite, H-USY and H-MCM-22
title_full Alkylation of phenol with methanol over H-ZSM-5, H-Beta, H-Mordenite, H-USY and H-MCM-22
title_fullStr Alkylation of phenol with methanol over H-ZSM-5, H-Beta, H-Mordenite, H-USY and H-MCM-22
title_full_unstemmed Alkylation of phenol with methanol over H-ZSM-5, H-Beta, H-Mordenite, H-USY and H-MCM-22
title_short Alkylation of phenol with methanol over H-ZSM-5, H-Beta, H-Mordenite, H-USY and H-MCM-22
title_sort alkylation of phenol with methanol over h zsm 5 h beta h mordenite h usy and h mcm 22
topic Chemical Engineering
url http://hdl.handle.net/11427/8595
work_keys_str_mv AT moongilliancatherine alkylationofphenolwithmethanoloverhzsm5hbetahmordenitehusyandhmcm22