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

0506758 - ÚFCH JH 2020 RIV US eng J - Článek v odborném periodiku
Gill, A. - Hong, C. - Gromadzki, Daniel - Marić, M.
Reactive compatibilization of poly(styrene-ran-acrylonitrile)/poly(ethylene) blends through the acid-epoxy reaction.
Journal of Applied Polymer Science. Roč. 133, č. 44 (2016), č. článku 44178. ISSN 0021-8995. E-ISSN 1097-4628
Institucionální podpora: RVO:61388955
Klíčová slova: nitroxide-mediated polymerization * styrene-acrylonitrile copolymers * glass-transition temperature * block-copolymers * interfacial-tension * poly(methyl methacrylate)
Obor OECD: Physical chemistry
Impakt faktor: 1.860, rok: 2016
Způsob publikování: Omezený přístup

Two 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.
Trvalý link: http://hdl.handle.net/11104/0297934