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Electron beam crosslinking of ethylene-octene copolymers

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dc.title Electron beam crosslinking of ethylene-octene copolymers en
dc.contributor.author Svoboda (FT), Petr
dc.contributor.author Svobodová, Dagmar
dc.contributor.author Mokrejš, Pavel
dc.contributor.author Vašek, Vladimír
dc.contributor.author Jantanasakulwong, Kittisak
dc.contributor.author Ougizawa, Toshiaki
dc.contributor.author Inoue, Takashi
dc.relation.ispartof Polymer
dc.identifier.issn 0032-3861 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2015
utb.relation.volume 81
dc.citation.spage 119
dc.citation.epage 128
dc.type article
dc.language.iso en
dc.publisher Elsevier
dc.identifier.doi 10.1016/j.polymer.2015.10.057
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0032386115303438
dc.subject Crosslinking en
dc.subject Electron beam irradiation en
dc.subject Ethylene-octene copolymer en
dc.description.abstract Seven ethylene-octene copolymers (EOC) with a wide range of octene content (17-45 wt. %) were crosslinked by e-beam radiation (in range 30-120 kGy). Testing methods included differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), high-temperature creep test, analysis of the gel content and rheology. It has been found that copolymers with higher initial molecular weight (or lower MFI) and higher branching density (or higher octene content) attain a higher level of crosslinking density. Increasing octene content brings about lower melting point (Tm), crystallization temperature (Tc), crystallinity (X), glass transition temperature (Tg) and storage modulus. Crosslinking influenced the properties below Tm only marginally. However, the properties above Tm were extremely influenced (high temperature creep). Above Tm (without the presence of crystals) only the chemical bonds hold the amorphous chains together which was manifested by creep gradually decreasing at 150 °C with an increasing irradiation level. Loss factor (tanδ at 0.1 Hz), which is a very important parameter in evaluation of molecular structure, was measured by rheology at 150 °C, and it revealed a decreasing trend (or increasing crosslinking level) with the increasing octene content, surprisingly regardless of the initial molecular weight (or MFI) at 120 kGy. © 2015 Elsevier Ltd. en
utb.faculty Faculty of Technology
utb.faculty Faculty of Humanities
utb.faculty Faculty of Applied Informatics
dc.identifier.uri http://hdl.handle.net/10563/1005765
utb.identifier.obdid 43874241
utb.identifier.scopus 2-s2.0-84948450978
utb.identifier.wok 000365813800014
utb.identifier.coden POLMA
utb.source j-scopus
dc.date.accessioned 2016-01-15T10:59:05Z
dc.date.available 2016-01-15T10:59:05Z
dc.description.sponsorship Internal Grant Agency of the Tomas Bata University in Zlin [IGA/FT/2015/007]
utb.contributor.internalauthor Svoboda (FT), Petr
utb.contributor.internalauthor Svobodová, Dagmar
utb.contributor.internalauthor Mokrejš, Pavel
utb.contributor.internalauthor Vašek, Vladimír
utb.fulltext.affiliation Petr Svoboda a*, Dagmar Svobodova b, Pavel Mokrejs a, Vladimir Vasek c, Kittisak Jantanasakulwong d, Toshiaki Ougizawa d, Takashi Inoue e a Department of Polymer Engineering, Faculty of Technology, Tomas Bata University in Zlin, Vavreckova 275, 762 72, Zlin, Czech Republic b Faculty of Humanities, Tomas Bata University in Zlin, Mostni 5139, 760 01, Zlin, Czech Republic c Faculty of Applied Informatics, Tomas Bata University in Zlin, Nad Stranemi 4511, 760 05, Zlin, Czech Republic d Department of Organic and Polymeric Materials, Tokyo Institute of Technology, 2-12-1-S8-33, Ookayama, Meguro-ku, Tokyo, 152-8552, Japan e Department of Polymer Sci. & Eng., Yamagata University, Yonezawa, 992-8510, Japan * Corresponding author. E-mail address: svoboda@ft.utb.cz (P. Svoboda).
utb.fulltext.dates Received 30 July 2015 Received in revised form 16 October 2015 Accepted 26 October 2015 Available online 4 November 2015
utb.fulltext.faculty Faculty of Technology
utb.fulltext.faculty Faculty of Humanities
utb.fulltext.faculty Faculty of Technology
utb.fulltext.faculty Faculty of Applied Informatics
utb.fulltext.ou Department of Polymer Engineering
utb.fulltext.ou Department of Polymer Engineering
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