Alkaline conventional and in situ transesterification of cottonseed oil for the production of biodiesel

dc.contributor.authorGeorgogianni, K. G.en
dc.contributor.authorKontominas, A. G.en
dc.contributor.authorPomonis, P. J.en
dc.contributor.authorAvlonitis, D.en
dc.contributor.authorGergis, V.en
dc.date.accessioned2015-11-24T16:44:45Z
dc.date.available2015-11-24T16:44:45Z
dc.identifier.issn0887-0624-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8832
dc.rightsDefault Licence-
dc.subjectacid methyl-estersen
dc.subjectsoybean oilen
dc.subjectvegetable-oilsen
dc.subjectcatalyzed transesterificationen
dc.subjectrapeseed oilen
dc.subjectseed oilen
dc.subjectkineticsen
dc.subjectfuelsen
dc.subjectphaseen
dc.titleAlkaline conventional and in situ transesterification of cottonseed oil for the production of biodieselen
heal.abstractIn the present work, the transesterification of cottonseed oil with methanol and ethanol, in the presence of alkali catalyst (NaOH), using low-frequency ultrasonication (24 KHz) and mechanical stirring (600 rpm) for the production of biodiesel fuel was studied. Both conventional and in situ transesterification were investigated. Use of ultrasonication in conventional transesterification with methanol gave high yields of methyl esters (95%) after a short reaction time (20 min) similar to those using mechanical stirring. Higher concentrations of NaOH (2.0%) gave higher ester yields. Use of ultrasonication in conventional transesterification with ethanol gave similar yields to those using mechanical stirring but significantly lower than respective yields using methanol. In the in situ transesterification, the use of ultrasonication and mechanical stirring led to similar high yields (95%) of methyl esters after approximately 20 min of reaction time. In the presence of ethanol, use of ultrasonication led to high ester yields (98%) in only 40 min of reaction time while use of mechanical stirring gave low yields (78%) even after 4 h of reaction time. In situ transesterification gave similar ester yields to those obtained by conventional transesterification being an efficient and economical process. Reaction rate constants were calculated, using first-order reaction kinetics, to be equal to 3.1 x 10(-3) s(-1) for conventional transesterification using methanol and 2.0% NaOH, and 7.0 x 10(-4) s(-1) using ethanol.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDoi 10.1021/Ef700784j-
heal.identifier.secondary<Go to ISI>://000256057600096-
heal.identifier.secondaryhttp://pubs.acs.org/doi/abs/10.1021/ef700784j-
heal.journalNameEnergy & Fuelsen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2008-
heal.publisherAmerican Chemical Societyen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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