Number of the records: 1  

Origin of toughness in .beta.-polypropylene: the effect of molecular mobility in the amorphous phase

  1. 1.
    SYSNO ASEP0440934
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleOrigin of toughness in .beta.-polypropylene: the effect of molecular mobility in the amorphous phase
    Author(s) Policianová, Olivia (UMCH-V) RID
    Hodan, Jiří (UMCH-V)
    Brus, Jiří (UMCH-V) RID, ORCID
    Kotek, Jiří (UMCH-V) RID
    Source TitlePolymer. - : Elsevier - ISSN 0032-3861
    Roč. 60, 9 March (2015), s. 107-114
    Number of pages8 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsisotactic polypropylene ; β-modification ; toughness
    Subject RIVJI - Composite Materials
    R&D ProjectsGA13-29009S GA ČR - Czech Science Foundation (CSF)
    Institutional supportUMCH-V - RVO:61389013
    UT WOS000351117300014
    EID SCOPUS84930487388
    DOI10.1016/j.polymer.2015.01.047
    AnnotationThis study aims to explore the origin of toughness in β-phase isotactic polypropylene (i-PP). Samples of commercial-grade i-PP, both neat and nucleated with a specific β-nucleating agent (N,N′-dicyclohexylnaphthalene-2,6-dicarboxamide), were subjected to a combination of structure-sensitive methods and fracture mechanical testing. In addition to common structural characterisation methods, solid-state NMR data were collected to obtain information about the dynamics of the polymer segments as well as the structure. In particular, temperate-induced transformation between the free and constrained amorphous phase was monitored by variable-temperature 13C MAS NMR, whereas T1ρ(1H) relaxation was used to estimate correlations times of segmental motions. Lower thermodynamic stability of rigid amorphous fraction was found in the β-crystalline systems. In contrast helical chains in crystalline and constrained amorphous phase were found to be more restrained in the α-crystalline system. Overall, the results indicate larger restrictions in chain mobility in the amorphous phase of the α-polymorphic PP system than in that of the β-crystalline ones.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2016
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.