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dc.citation.endPage 3600 -
dc.citation.number 22 -
dc.citation.startPage 3593 -
dc.citation.title JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY -
dc.citation.volume 54 -
dc.contributor.author Kim, Beomjin -
dc.contributor.author Lee, Dong Geun -
dc.contributor.author Kim, Dong Yeon -
dc.contributor.author Kim, Hyeok Jin -
dc.contributor.author Kong, Nam Sik -
dc.contributor.author Kim, Jin Chul -
dc.contributor.author Noh, Seung Man -
dc.contributor.author Jung, Hyun Wook -
dc.contributor.author Park, Young Il -
dc.date.accessioned 2023-12-21T23:08:29Z -
dc.date.available 2023-12-21T23:08:29Z -
dc.date.created 2016-10-07 -
dc.date.issued 2016-11 -
dc.description.abstract The new thermal radical initiators (TRIs) with linear and cyclic type groups based on derivatives of O-imino-isourea have been designed and synthesized. The radical polymerization property of the synthesized TRI derivatives as a radical initiator in n-butyl acrylate was monitored by differential scanning calorimetry analysis. TRI derivatives with linear type groups, such as 3-PenDCC, 3-HexDCC, and 4-HepDCC, showed peak temperatures (T-peak) of 80-84 degrees C, whereas those with cyclic type groups, such as C-PenDCC, C-HexDCC, and C-HepDCC, exhibited a wide T-peak distribution in the 74-87 degrees C range. The polymerization efficiency using new TRIs in n-butyl acrylate was elaborately identified from the molecular weights and conversion obtained using gel permeation chromatography analysis and NMR spectroscopy. To consider their possible application to automotive clearcoats, the real-time evolution of the rheological properties of clearcoat resins during the crosslinking process with newly synthesized TRI derivatives was measured, confirming the different crosslinking kinetics of TRI derivatives in real thermal curing process. The results were found to be well correlated with data from the radical polymerization experiments of TRIs. -
dc.identifier.bibliographicCitation JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, v.54, no.22, pp.3593 - 3600 -
dc.identifier.doi 10.1002/pola.28244 -
dc.identifier.issn 0887-624X -
dc.identifier.scopusid 2-s2.0-84988920692 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/20550 -
dc.identifier.url http://onlinelibrary.wiley.com/doi/10.1002/pola.28244/abstract -
dc.identifier.wosid 000386658400005 -
dc.language 영어 -
dc.publisher WILEY-BLACKWELL -
dc.title Thermal radical initiator derivatives based on O-imino-isourea: Synthesis, polymerization, and characterization -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Polymer Science -
dc.relation.journalResearchArea Polymer Science -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor DFT method -
dc.subject.keywordAuthor low temperature curing -
dc.subject.keywordAuthor O-imino-isourea -
dc.subject.keywordAuthor radical polymerization -
dc.subject.keywordAuthor rheology -
dc.subject.keywordAuthor initiators -
dc.subject.keywordAuthor thermal radical -
dc.subject.keywordAuthor initiator -
dc.subject.keywordPlus AUTOMOTIVE CLEARCOATS -
dc.subject.keywordPlus ACRYLATE -
dc.subject.keywordPlus DENSITY -
dc.subject.keywordPlus REDOX -

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