Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/19864
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dc.contributor.authorWENN, Benjamin-
dc.contributor.authorREEKMANS, Gunter-
dc.contributor.authorADRIAENSENS, Peter-
dc.contributor.authorJUNKERS, Tanja-
dc.date.accessioned2015-12-01T09:27:19Z-
dc.date.available2015-12-01T09:27:19Z-
dc.date.issued2015-
dc.identifier.citationMACROMOLECULAR RAPID COMMUNICATIONS, 36 (16), p. 1479-1485-
dc.identifier.issn1022-1336-
dc.identifier.urihttp://hdl.handle.net/1942/19864-
dc.description.abstractThe branching stemming from midchain radical formation in n-butyl acrylate polymerization is investigated via melt-state C-13 NMR measurements. The dependence of the degree of branching (DB) on the monomer conversion of the system is examined for photoinduced polymerizations, revealing a steady increase in branching with conversion. For polymerization at moderate light intensities, an increase in branching from 0.03% to 0.37% is observed for polymerizations at 60 degrees C, which is fivefold below the level of branching observed in thermally initiated polymerizations under otherwise identical reaction conditions. The reason for this overall reduction in branching remains momentarily unclear; yet, a strong dependence of branching on light intensity is observed. While polymerization under a 1 W LED lamp results at almost full monomer conversion in branching degrees of 0.22%, polymerization under a 400 W lamp yields 1.81% of chain branches.-
dc.description.sponsorshipThe authors are grateful for funding in the framework of the European Science Foundation-Precision Polymer Materials (P2M) program. Additional support by the Belgian Science Policy via the Interuniversity Attraction Poles Program IAP-PAI P7/05 "Functional Supramolecular Systems" is also kindly acknowledged.-
dc.language.isoen-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.rights© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim-
dc.subject.otheracrylates; kinetics (polym.); midchain radicals; NMR spectroscopy; photopolymerizations-
dc.titlePhotoinduced Acrylate Polymerization: Unexpected Reduction in Chain Branching-
dc.typeJournal Contribution-
dc.identifier.epage1485-
dc.identifier.issue16-
dc.identifier.spage1479-
dc.identifier.volume36-
local.format.pages7-
local.bibliographicCitation.jcatA1-
dc.description.notes[Wenn, Benjamin; Junkers, Thomas] Univ Hasselt, Inst Mat Res IMO, Polymer React Design Grp, B-3590 Diepenbeek, Belgium. [Reekmans, Gunter; Adriaensens, Peter] Univ Hasselt, Inst Mat Res IMO, Nucl Magnet Resonance Spect Grp, B-3590 Diepenbeek, Belgium. [Adriaensens, Peter; Junkers, Thomas] IMEC, Associated Lab IMOMEC, B-3590 Diepenbeek, Belgium.-
local.publisher.placeWEINHEIM-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1002/marc.201500198-
dc.identifier.isi000359793200004-
item.contributorWENN, Benjamin-
item.contributorREEKMANS, Gunter-
item.contributorADRIAENSENS, Peter-
item.contributorJUNKERS, Tanja-
item.validationecoom 2016-
item.fullcitationWENN, Benjamin; REEKMANS, Gunter; ADRIAENSENS, Peter & JUNKERS, Tanja (2015) Photoinduced Acrylate Polymerization: Unexpected Reduction in Chain Branching. In: MACROMOLECULAR RAPID COMMUNICATIONS, 36 (16), p. 1479-1485.-
item.accessRightsRestricted Access-
item.fulltextWith Fulltext-
crisitem.journal.issn1022-1336-
crisitem.journal.eissn1521-3927-
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