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Borate-assisted liquid-phase selective oxidation of n-pentane

dc.contributor.authorAworinde, SM
dc.contributor.authorWang, K
dc.contributor.authorLapkin, AA
dc.contributor.orcidAworinde, Samson [0000-0001-5774-9782]
dc.contributor.orcidLapkin, Alexei [0000-0001-7621-0889]
dc.date.accessioned2018-10-10T05:19:46Z
dc.date.available2018-10-10T05:19:46Z
dc.date.issued2018
dc.description.abstractOxidation of n-pentane with molecular oxygen to sec-pentanols was performed in the presence of a free radical initiator (di-tert-butyl peroxide) and a boron compound (sec-butyl metaborate), with in situ adsorption of water on molecular sieve 3A. Kinetics of the reaction was studied in a laboratory-scale batch reactor over a broad range of conditions (130‒150°C, 20‒30 bar, 5‒10 vol% "O" _"2" ) in order to establish the optimum parameters for maximising the selectivity and yield of sec-pentanols. Results show that the initiator markedly improves the rate of oxidation, and hence yield, compared to thermal oxidation without an initiator, while the boron species enhances the selectivity to sec-pentanols. Under the conditions investigated, maximum sec-pentanol selectivity is 56% with an alcohol-to-ketone ratio of 3.6:1 for the borate-assisted oxidation compared to 33% and 1.1:1, respectively, for the oxidation without borate. This work demonstrates the feasibility of oxyfunctionalization of n-pentane with industrially relevant selectivity and yield.
dc.description.sponsorshipExxonMobil
dc.identifier.doi10.17863/CAM.30827
dc.identifier.eissn1873-3875
dc.identifier.issn0926-860X
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/283460
dc.language.isoeng
dc.publisherElsevier BV
dc.publisher.urlhttp://dx.doi.org/10.1016/j.apcata.2018.06.023
dc.subjectSelective oxidation
dc.subjectn-Pentane
dc.subjectBorate ester
dc.subjectInitiator
dc.subjectSelectivity
dc.titleBorate-assisted liquid-phase selective oxidation of n-pentane
dc.typeArticle
dcterms.dateAccepted2018-06-12
prism.endingPage42
prism.publicationDate2018
prism.publicationNameApplied Catalysis A: General
prism.startingPage28
prism.volume563
rioxxterms.licenseref.startdate2018-08-05
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.typeJournal Article/Review
rioxxterms.versionAM
rioxxterms.versionofrecord10.1016/j.apcata.2018.06.023

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