The pre‐separation of oxygen containing compounds in oxidised heavy paraffinic fractions and their identification by GC‐MS with supersonic molecular beams

dc.contributor.authorPotgieter, Hein
dc.contributor.authorDe Coning, Piet
dc.contributor.authorBekker, Riaan
dc.contributor.authorRohwer, Egmont Richard
dc.contributor.authorAmirav, Aviv
dc.date.accessioned2019-07-24T07:37:44Z
dc.date.issued2019-04
dc.descriptionSupplementary material: Figure A: Mass spectra of n‐eicosane with conventional EI (bottom) and cold‐EI (top). Figure B: Mass spectra of n‐docosane with conventional EI (bottom) and cold‐EI (top). Figure C: Mass spectra of n‐eicosene with conventional EI (bottom) and cold‐EI (top). Figure D: Mass spectra of undecanoic acid with conventional EI (bottom) and cold‐EI (top). Figure E: Mass spectra of tetradecanoic acid with conventional EI (bottom) and cold‐EI (top). Figure F: Mass spectra of 1‐tetradecanol with conventional EI (bottom) and cold‐EI (top). Figure G: Mass spectra of 1‐hexadecanol with conventional EI (bottom) and cold‐EI (top). Figure H: Mass spectra of 1‐heptadecanol with conventional EI (bottom) and cold‐EI (top). Figure I: Mass spectra of 1‐octadecanol with conventional EI (bottom) and cold‐EI (top). Figure J: Mass spectra of 1‐eicosanol with conventional EI (bottom) and cold‐EI (top). Figure K: Mass spectra of 1‐docosanol with conventional EI (bottom) and cold‐EI (top). Figure L: Mass spectra of 2‐hexadecanone at 16.8 min (distribution 1) with conventional EI (bottom) and cold‐EI (top). Figure M: Mass spectra of 2‐heptadecanone at 18.8 min (distribution 1) with conventional EI (bottom) and cold‐EI (top). Figure N: Mass spectra of γ‐stearolactone at 25.1 min (distribution 2) with conventional EI (bottom) and cold‐EI (top). Figure O: Mass spectra of the oxygenate eluting at 45.5 min (distribution 3) with conventional EI (bottom) and cold‐EI (top). Figure P: Mass spectra of the oxygenate eluting at 46.5 min (distribution 3) with conventional EI (bottom) and cold‐EI (top).en_ZA
dc.description.abstractThe heavy petroleum fractions produced during refining processes need to be upgraded to useable products to increase their value. Hydrogenated heavy paraffinic fractions can be oxidised to produce high value products that contain a variety of oxygenates. These heavy oxygenated paraffinic fractions need to be characterised to enable the control of oxidation processes and to understand product properties. The accurate identification of the oxygenates present in these fractions by electron ionisation (EI) mass spectrometry is challenging due to the complexity of these heavy fractions. Adding to this challenge is the limited applicability of EI mass spectral libraries due to the absence of molecular ions from the EI mass spectra of many oxygenates. The separation of oxygenates from the complex hydrocarbon matrix prior to high temperature GC‐MS (HT‐GC‐MS) analysis reduces the complexity of these fractions and assists in the accurate identification of these oxygenates. Solid phase extraction (SPE) and supercritical fluid chromatography (SFC) were employed as prefractionation techniques. GC‐MS with supersonic molecular beams (SMBs) (also named GC‐MS with cold‐EI) utilises a SMB interface with which EI is done with vibrationally cold sample compounds in a fly‐through ion source (cold‐EI) resulting in a substantial increase in the molecular ion signal intensity in the mass spectrum. This greatly enhances the accurate identification of the oxygenates in these fractions. This study investigated the ionisation behaviour of oxygenated compounds using cold‐EI. The prefractionation by SPE and SFC and the subsequent analysis with GC‐MS with cold‐EI were applied to an oxygenated heavy paraffinic fraction.en_ZA
dc.description.departmentChemistryen_ZA
dc.description.embargo2020-04-01
dc.description.librarianhj2019en_ZA
dc.description.urihttp://wileyonlinelibrary.com/journal/jmsen_ZA
dc.identifier.citationPotgieter H, de Coning P, Bekker R, Rohwer E, Amirav A. The pre‐separation of oxygen containing compounds in oxidised heavy paraffinic fractions and their identification by GC‐MS with supersonic molecular beams. Journal of Mass Spectrometry 2019;54:328–341. https://doi.org/10.1002/jms.4340.en_ZA
dc.identifier.issn1076-5174 (print)
dc.identifier.issn1096-9888 (online)
dc.identifier.other10.1002/jms.4340
dc.identifier.urihttp://hdl.handle.net/2263/70783
dc.language.isoenen_ZA
dc.publisherWileyen_ZA
dc.rights© 2019 John Wiley & Sons, Ltd. This is the pre-peer reviewed version of the following article : The pre‐separation of oxygen containing compounds in oxidised heavy paraffinic fractions and their identification by GC‐MS with supersonic molecular beams. Journal of Mass Spectrometry 2019;54:328–341. https://doi.org/10.1002/jms.4340. The definite version is available at : http://wileyonlinelibrary.com/journal/jms.en_ZA
dc.subjectHeavy paraffinic fractionsen_ZA
dc.subjectMass spectrometry with supersonic molecular beamen_ZA
dc.subjectOxygen-containing compoundsen_ZA
dc.subjectElectron ionisation (EI)en_ZA
dc.subjectSolid phase extraction (SPE)en_ZA
dc.subjectSupercritical fluid chromatography (SFC)en_ZA
dc.subjectSupersonic molecular beam (SMB)en_ZA
dc.titleThe pre‐separation of oxygen containing compounds in oxidised heavy paraffinic fractions and their identification by GC‐MS with supersonic molecular beamsen_ZA
dc.typePostprint Articleen_ZA

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