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Isothermal crystallization in polypropylene/ethylene-octene copolymer blends

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dc.title Isothermal crystallization in polypropylene/ethylene-octene copolymer blends en
dc.contributor.author Svoboda (FT), Petr
dc.contributor.author Trivedi, Krunal
dc.contributor.author Svobodová, Dagmar
dc.contributor.author Mokrejš, Pavel
dc.contributor.author Vašek, Vladimír
dc.contributor.author Mori, Keisuke
dc.contributor.author Ougizawa, Toshiaki
dc.contributor.author Inoue, Takashi
dc.relation.ispartof Materials Chemistry and Physics
dc.identifier.issn 0254-0584 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2011
utb.relation.volume 131
utb.relation.issue 1-2
dc.citation.spage 84
dc.citation.epage 93
dc.type article
dc.language.iso en
dc.publisher Elsevier Science SA en
dc.identifier.doi 10.1016/j.matchemphys.2011.07.058
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0254058411006523
dc.subject crystallization en
dc.subject electron microscopy (TEM) en
dc.subject optical microscopy en
dc.subject nucleation en
dc.description.abstract Crystallization kinetics of polypropylene (PP)/ethylene-octene copolymer (EOC) blends was measured by differential scanning calorimetry (DSC) and by optical microscopy at various temperatures (123-140 degrees C). By DSC it was found that small amounts of EOC (10-30%) increase the bulk crystallization kinetics; in some cases even 80% increase was observed. Larger amounts of EOC (50-80%) have caused a decrease in crystallization kinetics. Optical microscopy has revealed that crystallization kinetics of a single spherulite is decreased by the presence of EOC, and at the same time there are more spherulites in the blend. EOC acts as a nucleation agent increasing the bulk crystallization rate and at the same time it acts as an obstacle to the growing front of a spherulite when the PP lamellae have to go around the EOC obstacle. This was confirmed by detailed analyses according to Avrami and Hoffman-Lauritzen. Structure was also observed by transmission electron microscopy (TEM). At low PP content (20%) PP forms very small isolated particles with size smaller than 1 micrometer. At 40% of PP a structure resembling a co-continuous one was found. When the PP is a majority phase (20-40% of EOC) rather large EOC particles were found. TEM also revealed presence of PP lamellae in EOC regions that together with T(g) shift of PP and also EOC suggested partial miscibility. While at low temperatures the crystallization is very fast, at higher temperatures there is a competition of phase separation and crystallization. (C) 2011 Elsevier B.V. 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/10563/1002702
utb.identifier.rivid RIV/70883521:28110/11:43867026!RIV12-MSM-28110___
utb.identifier.rivid RIV/70883521:28140/11:43867026!RIV12-MSM-28140___
utb.identifier.rivid RIV/70883521:28150/11:43867026!RIV12-MSM-28150___
utb.identifier.obdid 43866472
utb.identifier.scopus 2-s2.0-84865766833
utb.identifier.wok 000298764800017
utb.identifier.coden MCHPD
utb.source j-wok
dc.date.accessioned 2012-02-13T11:09:16Z
dc.date.available 2012-02-13T11:09:16Z
utb.contributor.internalauthor Svoboda (FT), Petr
utb.contributor.internalauthor Trivedi, Krunal
utb.contributor.internalauthor Svobodová, Dagmar
utb.contributor.internalauthor Mokrejš, Pavel
utb.contributor.internalauthor Vašek, Vladimír
utb.fulltext.affiliation Petr Svobodaa,∗, Krunal Trivedi a, Dagmar Svobodovaa, Pavel Mokrejs a, Vladimir Vasek b, Keisuke Mori c, Toshiaki Ougizawac, Takashi Inoue d 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 d Dept. of Polymer Sci. & Eng., Yamagata University, Yonezawa 992-8510, Japan
utb.fulltext.dates Received 27 September 2010 Received in revised form 11 July 2011 Accepted 24 July 2011
utb.fulltext.sponsorship This work has been supported by theMinistry 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 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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