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Cross-linking kinetics study and high temperature mechanical properties of ethylene-octene copolymer (EOC)/dicumylperoxide(DCP) system

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dc.title Cross-linking kinetics study and high temperature mechanical properties of ethylene-octene copolymer (EOC)/dicumylperoxide(DCP) system en
dc.contributor.author Poongavalappil, Sameepa
dc.contributor.author Svoboda (FT), Petr
dc.contributor.author Theravalappil, Rajesh
dc.contributor.author Svobodová, Dagmar
dc.contributor.author Vašek, Vladimír
dc.contributor.author Jantanasakulwong, Kittisak
dc.contributor.author Ougizawa, Toshiaki
dc.relation.ispartof European Polymer Journal
dc.identifier.issn 0014-3057 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2011
utb.relation.volume 47
utb.relation.issue 10
dc.citation.spage 1949
dc.citation.epage 1955
dc.type article
dc.language.iso en
dc.publisher Pergamon Elsevier Science Ltd. en
dc.identifier.doi 10.1016/j.eurpolymj.2011.07.006
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0014305711002540
dc.subject creep en
dc.subject cross-linking en
dc.subject dicumylperoxide en
dc.subject DMA en
dc.subject ethylene-octene copolymer en
dc.subject RPA en
dc.description.abstract Ethylene-octene copolymer (EOC) was cross-linked by dicumyl peroxide (DCP) at various temperatures (150-200 °C). Six concentrations of DCP in range 0.2-0.7 wt.% were investigated. Cross-linking was studied by rubber process analyzer (RPA). From RPA data analysis real part modulus s′, tan(delta) and reaction rate constant K were investigated as a function of peroxide content and temperature. The highest s′max and the lowest tan(delta) were found for 0.7% of DCP at 150 °C. The quantitative analysis confirmed that the DCP-EOC cross-linking was occurring as first order reaction. The highest cross-linking kinetics constant K was found for 0.6% of peroxide at 200 °C. The activation energy of cross-linking EA obtained by Arrhenius plot had maximum at 0.5-0.6% of peroxide. While at 190-200 °C temperature range there was no detectable degradation for 0.2% of peroxide, for 0.4-0.7% of peroxide there was increasing level of degradation with increasing peroxide content. Generally, at low temperatures (150-180 °C) the increasing peroxide content caused increase in cross-linking kinetics. However at higher temperatures (190-200 °C) increase in kinetics (for 0.2-0.5% of peroxide) was followed by decrease. Especially in 0.6-0.7% peroxide level range the cross-linking is in competition with degradation which lowers the overall cross-linking kinetics. Gel content of the cross-linked EOC samples was found to be increasing with increase in peroxide content, which is caused by the increased cross-link network. Cross-linked samples were subjected to creep studies at elevated temperature (150 °C) and the result was found in agreement with the gel content and RPA results. Storage modulus and tan(delta) values obtained by Dynamic Mechanical Analysis (DMA) also support the RPA results. © 2011 Elsevier Ltd. All rights reserved. en
utb.faculty Faculty of Technology
utb.faculty Faculty of Applied Informatics
utb.faculty Faculty of Humanities
dc.identifier.uri http://hdl.handle.net/10563/1002644
utb.identifier.rivid RIV/70883521:28110/11:43865623!RIV13-MSM-28110___
utb.identifier.rivid RIV/70883521:28140/11:43865623!RIV13-MSM-28140___
utb.identifier.rivid RIV/70883521:28150/11:43865623!RIV13-MSM-28150___
utb.identifier.obdid 43865637
utb.identifier.scopus 2-s2.0-80052950986
utb.identifier.wok 000295659600010
utb.identifier.coden EUPJA
utb.source j-scopus
dc.date.accessioned 2012-02-10T13:15:22Z
dc.date.available 2012-02-10T13:15:22Z
utb.contributor.internalauthor Poongavalappil, Sameepa
utb.contributor.internalauthor Svoboda (FT), Petr
utb.contributor.internalauthor Theravalappil, Rajesh
utb.contributor.internalauthor Svobodová, Dagmar
utb.contributor.internalauthor Vašek, Vladimír
utb.fulltext.affiliation Sameepa Poongavalappil a, Petr Svoboda a,*, Rajesh Theravalappil a, Dagmar Svobodova a,Vladimir Vasek b, Kittisak Jantanasakulwong c, Toshiaki Ougizawa c a Centre of Polymer Systems, Faculty of Technology, Tomas Bata University in Zlin, Nam. T.G. Masaryka 5555, 760 01 Zlin, Czech Republic b Faculty of Applied Informatics, Tomas Bata University in Zlin, Nad Stranemi 4511, 760 05 Zlin, Czech Republic c Department of Organic and Polymeric Materials, Tokyo Institute of Technology, 2-12-1-S8-33, Ookayama, Meguro-ku, Tokyo 152-8552, Japan * Corresponding author. Tel.: +420 576 031 335; fax: +420 577 210 172. E-mail address: [email protected] (P. Svoboda).
utb.fulltext.dates Received 23 February 2011 Received in revised form 4 May 2011 Accepted 5 July 2011 Available online 23 July 2011
utb.fulltext.sponsorship This work has been supported by the Ministry of Education of the Czech Republic as a part of the project No. VZ MSM 7088352102, Internal Grant Agency (IGA/23/FT/11/ D) and also by Operational Programme Research and Development for Innovations co-funded by the European Regional Development Fund (ERDF) and national budget of Czech Republic within the framework of the Centre of Polymer Systems project (Reg. number: CZ.1.05/2.1.00/ 03.0111).
utb.fulltext.projects VZ MSM 7088352102
utb.fulltext.projects IGA/23/FT/11/D
utb.fulltext.projects CZ.1.05/2.1.00/ 03.0111
utb.fulltext.faculty Faculty of Technology
utb.fulltext.faculty Faculty of Applied Informatics
utb.fulltext.ou Centre of Polymer Systems
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