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Reactive compatibilization of poly(styrene-ran-acrylonitrile)/poly(ethylene) blends through the acid-epoxy reaction

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    SYSNO ASEP0506758
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleReactive compatibilization of poly(styrene-ran-acrylonitrile)/poly(ethylene) blends through the acid-epoxy reaction
    Author(s) Gill, A. (CA)
    Hong, C. (CA)
    Gromadzki, Daniel (UFCH-W)
    Marić, M. (CA)
    Article number44178
    Source TitleJournal of Applied Polymer Science. - : Wiley - ISSN 0021-8995
    Roč. 133, č. 44 (2016)
    Number of pages12 s.
    Languageeng - English
    CountryUS - United States
    Keywordsnitroxide-mediated polymerization ; styrene-acrylonitrile copolymers ; glass-transition temperature ; block-copolymers ; interfacial-tension ; poly(methyl methacrylate)
    Subject RIVCF - Physical ; Theoretical Chemistry
    OECD categoryPhysical chemistry
    Method of publishingLimited access
    Institutional supportUFCH-W - RVO:61388955
    UT WOS000383356200005
    EID SCOPUS84979752646
    DOI10.1002/app.44178
    AnnotationTwo families of acid functional styrene/acrylonitrile copolymers (SAN) for application as dispersed phase barrier materials in poly(ethylene) (PE) were studied. One type is SAN made by nitroxide mediated polymerization (NMP), which was subsequently chain extended with a styrene/tert-butyl acrylate (S/tBA) mixture to provide a block copolymer (number average molecular weight M-n = 36.6 kg mol 21 and dispersity D = 1.34, after which the tert-butyl protecting groups were converted to acid groups (SAN-b-S/AA). The other acid functional SAN is made by conventional radical terpolymerization (SAN-AA). SAN-AA and SAN-b-S/AA were each melt blended with PE grafted with epoxy functional glycidyl methacrylate (PE-GMA) at 160 degrees C in a twin screw extruder (70: 30 wt % PE-GMA: SAN co/terpolymer). The non-reactive PE-g-GMA/SAN blend had a volume to surface area diameter D (vs) 53.0 mu m while the reactive blends (via epoxy/acid coupling) (PE-GMA/SAN-b-SAA and PE-GMA/SAN-AA) had D (vs) 51.7 mu m and 1.1 mu m, respectively. After thermal annealing, the non-reactive blend coarsened dramatically while the reactive blends showed little signs of coarsening, suggesting that the acid/epoxy coupling was effective for morphological stability. (C) 2016 Wiley Periodicals, Inc.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2020
    Electronic addresshttp://hdl.handle.net/11104/0297934
Number of the records: 1  

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