Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/24964
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dc.contributor.authorHAVEN, Joris-
dc.contributor.authorZAQUEN, Neomy-
dc.contributor.authorRUBENS, Maarten-
dc.contributor.authorJUNKERS, Tanja-
dc.date.accessioned2017-10-10T07:29:52Z-
dc.date.available2017-10-10T07:29:52Z-
dc.date.issued2017-
dc.identifier.citationMacromolecular Reaction Engineering, 11(4), p. 1-12 (Art N° 1700016)-
dc.identifier.issn1862-832X-
dc.identifier.urihttp://hdl.handle.net/1942/24964-
dc.description.abstractThe high-temperature trithiocarbonate-mediated reversible addition-fragmentation chain transfer (RAFT) polymerization of n-butyl acrylate is studied using a high-resolution mass spectrometric on-line monitoring method. Therefore, an Orbitrap mass spectrometer, ideally suited for polymer analysis, is coupled to a continuous flow microreactor. Via adjustment of flow rates in the reactor, time sweep experiments can be carried out to allow monitoring a whole polymerization in a single experiment. The n-butyl acrylate polymerization is monitored in a temperature interval between 100 and 190 degrees C for reaction times between 1 and 10 minutes. In all cases, full mono-mer conversions are reached and even at the highest temperatures still relatively good molecular weight control and reasonably low dispersities are obtained. End group analysis from mass spectrometry reveals, however, that the desired RAFT product is already at the lower temperatures less abundant than some side products. The herein described on-line monitoring technique gives access to quasi-continuous data acquisition, and is found to be very robust, and low in scattering when compared to classical batch sampling techniques.-
dc.description.sponsorshipN.Z. is grateful for the funding from the 'Agency for Innovation by Science and Technology' in Flanders (IWT). The authors are grateful for funding from the Fonds Wetenschappelijk Onderzoek (FWO) in the form of project grants and personal scholarships (M.R.). J.H. is grateful for support via the BOF funds of Hasselt University.-
dc.language.isoen-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.rights© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim-
dc.subject.otheracrylate polymerization; continuous flow; mass spectrometry; microreactor; online monitoring-
dc.subject.otheracrylate polymerization; continuous flow; mass spectrometry; microreactor; online monitoring-
dc.titleThe Kinetics of n-Butyl Acrylate Radical Polymerization Revealed in a Single Experiment by Real Time On-line Mass Spectrometry Monitoring-
dc.typeJournal Contribution-
dc.identifier.epage12-
dc.identifier.issue4-
dc.identifier.spage1-
dc.identifier.volume11-
local.format.pages12-
local.bibliographicCitation.jcatA1-
dc.description.notes[Haven, Joris J.; Zaquen, Neomy; Rubens, Maarten; Junkers, Tanja] Univ Hasselt, Polymer React Design Grp, Inst Mat Res IMO IMOMEC, Agoralaan Bldg D, B-3590 Diepenbeek, Belgium. [Junkers, Tanja] IMEC Associated Lab IMOMEC, Wetenschapspk 1, B-3590 Diepenbeek, Belgium.-
local.publisher.placeWEINHEIM-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.bibliographicCitation.artnr1700016-
dc.identifier.doi10.1002/mren.201700016-
dc.identifier.isi000409302700008-
item.contributorHAVEN, Joris-
item.contributorZAQUEN, Neomy-
item.contributorRUBENS, Maarten-
item.contributorJUNKERS, Tanja-
item.validationecoom 2018-
item.fullcitationHAVEN, Joris; ZAQUEN, Neomy; RUBENS, Maarten & JUNKERS, Tanja (2017) The Kinetics of n-Butyl Acrylate Radical Polymerization Revealed in a Single Experiment by Real Time On-line Mass Spectrometry Monitoring. In: Macromolecular Reaction Engineering, 11(4), p. 1-12 (Art N° 1700016).-
item.accessRightsRestricted Access-
item.fulltextWith Fulltext-
crisitem.journal.issn1862-832X-
crisitem.journal.eissn1862-8338-
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