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Reactive compatibilization of poly(methyl acrylate‐ran‐acrylonitrile)/poly(ethylene) blends through amine–anhydride coupling
Authors:Amardeep Gill  Milan Mari?
Affiliation:Department of Chemical Engineering, McGill University, McGill Institute of Advanced Materials (MIAM), Center for Self‐Assembled Chemical Structures (CSACS), Montreal, QC, Canada
Abstract:Methyl acrylate/acrylonitrile copolymers (MA/AN) were reactively compatibilized as the dispersed phase into poly(ethylene) (PE) for potential hydrocarbon barrier materials. The MA/AN was made reactive by including p‐aminostyrene (PAS), yielding terpolymers (MA/AN/PAS) with pendant primary amine functionality (number average molecular weight urn:x-wiley:00218995:media:app44177:app44177-math-0001 = 65–133 kg mol?1, dispersity (?)=1.83–2.53, molar composition of PAS in copolymer FPAS = 0.03–0.14, molar composition of AN = FAN = 0.27–0.52). The non‐functional MA/AN and amino functional MA/AN/PAS were each melt blended into PE that was grafted with maleic anhydride (PE‐g‐MAnn) at 200 °C at 70:30 wt % PE‐g‐MAnn:co/terpolymer. After extrusion, the dispersed phase particle size (volume to surface area diameter, urn:x-wiley:00218995:media:app44177:app44177-math-0002) was coarse (12.6 μm) for the non‐reactive blend whereas it was much lower for the reactive blend ( urn:x-wiley:00218995:media:app44177:app44177-math-0003= 1.2 μm). Coarsening after annealing at 150 °C was slow, but the domain sizes increased only slightly for both cases. The reactive blend was deemed sufficiently stable and thus was suitable as a candidate barrier material for further testing against olefins. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44177.
Keywords:blends  compatibilization  copolymers  functionalization of polymers  radical polymerization
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