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Orientation of HDPE inclusions within solid-state drawn rubber-modified isotactic polypropylene: DSC insight

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dc.title Orientation of HDPE inclusions within solid-state drawn rubber-modified isotactic polypropylene: DSC insight en
dc.contributor.author Sližová, Marta
dc.contributor.author Raab, Miroslav
dc.relation.ispartof Journal of Applied Polymer Science
dc.identifier.issn 0021-8995 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2013
utb.relation.volume 130
utb.relation.issue 1
dc.citation.spage 603
dc.citation.epage 609
dc.type article
dc.language.iso en
dc.publisher John Wiley & Sons, Inc. en
dc.identifier.doi 10.1002/app.39207
dc.relation.uri http://onlinelibrary.wiley.com/doi/10.1002/app.39207/pdf
dc.subject blends en
dc.subject differential scanning calorimetry en
dc.subject orientation en
dc.subject polyolefins en
dc.subject structure-property relations en
dc.description.abstract Effect of drawing temperature on the melting behavior of oriented isotactic polypropylene (PP) modified with ethylene-propylene-diene monomer rubber with a small amount of high-density polyethylene (HDPE) is explored in this study. Injection-molded specimens both neat and 8 vol % modified PP were solid-state drawn to natural drawing ratio and characterized by X-ray diffraction, dynamic mechanical analysis (DMA), Charpy impact test and differential scanning calorimetry (DSC). A synergy of orientation and embedding rubber particles caused a significant increase of low-temperature notched impact strength of oriented blends. It was shown, that the DSC method can be used successfully for the indirect but very sensitive characterization of orientation on a nanometre scale. At the drawing temperature of 120°C, the DSC data indicated an incomplete transition of the PP crystalline structure: This is reflected by splitting and shifting of the melting peak of PP. An increase of the melting temperature of the HDPE inclusions by 3.5°C reflects the high orientation. © 2013 Wiley Periodicals, Inc. en
utb.faculty Faculty of Technology
dc.identifier.uri http://hdl.handle.net/10563/1003362
utb.identifier.obdid 43869977
utb.identifier.scopus 2-s2.0-84879896083
utb.identifier.wok 000321305500072
utb.identifier.coden JAPNA
utb.source j-scopus
dc.date.accessioned 2013-07-27T14:55:26Z
dc.date.available 2013-07-27T14:55:26Z
utb.contributor.internalauthor Sližová, Marta
utb.fulltext.affiliation Kucharczyk Pavel,1,2* Urbankova Miroslava, 1 Stloukal Petr,2,3 Koutny Marek,2,3 Sedlarik Vladimir1,2 1 Polymer Centre, Faculty of Technology, Tomas Bata University in Zlin, Nam. T.G. Masaryka 275, 76272 Zlín, Czech Republic 2 Centre of Polymer Systems, Polymer Centre, Tomas Bata University in Zlin, nam. T.G. Masaryka 5555, 760 01 Zlin,Czech Republic 3 Department of Environmental Protection Engineering, Centre of Polymer Systems, Tomas Bata University in Zlin, nam. T.G. Masaryka 5555, 76001 Zlin, Czech Republic *Correspondence to: K. Pavel (E-mail: p_kucharczyk@ft.utb.cz)
utb.fulltext.dates Received 16 October 2012 accepted 10 January 2013 published online 8 March 2013
utb.fulltext.sponsorship This work was funded by the Internal Grant Agency of Tomas Bata University in Zlin ( IGA/FT/2012/005) and Operational Program Research and Development for Innovations co-funded by the European Regional Development Fund (ERDF, project No. CZ.1.05/2.1.00/03.0111).
utb.scopus.affiliation Sližová M., Department of Physics and Materials Engineering, Faculty of Technology, Tomas Bata University in Zlin, 760 05 Zlin, Nad Stranemi 4511, Czech Republic; Raab M., Institute of Macromolecular Chemistry, AS CR, V.v.i., 162 06 Prague 6, Heyrovsky Sq. 2, Czech Republic
utb.fulltext.faculty Faculty of Technology
utb.fulltext.ou Centre of Polymer Systems
utb.fulltext.ou Polymer Centre
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