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dc.contributor.authorHallman, Christian
dc.contributor.authorVan Aarssen, Bernardus
dc.contributor.authorGrice, Kliti
dc.date.accessioned2017-01-30T14:45:52Z
dc.date.available2017-01-30T14:45:52Z
dc.date.created2009-05-14T02:17:13Z
dc.date.issued2008
dc.identifier.citationHallman, Christian and Van Aarssen, Bernardus and Grice, Kliti. 2008. Relative efficiency of free fatty acid butyl esterification: choice of catalyst and derivatisation procedure. Journal of Chromatography A. 1198-1199: pp. 14-20.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/40815
dc.identifier.doi10.1016/j.chroma.2008.05.030
dc.description.abstract

The conversion efficiency of alkanoic, alkenoic, branched, alicyclic, aromatic, keto-substituted, and dioic carboxylic acids to their corresponding butyl esters was compared under different reaction conditions (time, temperature, catalyst). We show that boron trifluoride is generally a more efficient catalyst than sulphuric acid. However, optimum derivatisation conditions vary strongly for different acids and no single derivatisation protocol can be employed without certain losses. Therefore, care must be taken when the simultaneous quantitative analysis of different types of carboxylic acids in one sample is envisaged.Addition of water-scavenging reagents to the reaction mixture caused the formation of artefacts andselectively decreased reaction yields.

dc.publisherElsevier
dc.subjectboron trifluoride
dc.subjectbutyl ester
dc.subjectfischer esterification
dc.subjectderivatisation
dc.subjectcarboxylic acid
dc.titleRelative efficiency of free fatty acid butyl esterification: choice of catalyst and derivatisation procedure
dc.typeJournal Article
dcterms.source.volume1198-1199
dcterms.source.startPage14
dcterms.source.endPage20
dcterms.source.issn00219673
dcterms.source.titleJournal of Chromatography A
curtin.note

The link to the journal's home page is: http://www.elsevier.com/wps/find/journaldescription.cws_home/502688/description#description

curtin.note

Copyright © 2008 Elsevier B.V. All rights reserved.

curtin.accessStatusFulltext not available
curtin.facultyDepartment of Applied Chemistry
curtin.facultySchool of Science
curtin.facultyFaculty of Science and Engineering


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