首页> 外文期刊>Journal of Applied Polymer Science >Dynamic Mechanical and Morphological Behavior ofBlends of Polystyrene and Polyacrylonitrile-g-(ethylene-co-propylene-co-diene)-g-styrene Prepared by in SituPolymerization of Styrene
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Dynamic Mechanical and Morphological Behavior ofBlends of Polystyrene and Polyacrylonitrile-g-(ethylene-co-propylene-co-diene)-g-styrene Prepared by in SituPolymerization of Styrene

机译:苯乙烯原位聚合制备的聚苯乙烯与聚丙烯腈-g-(乙烯-共丙烯-二烯)-g-苯乙烯共混物的动态力学和形貌行为

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摘要

PS/AES blends were prepared by in situpolymerization of styrene in the presence of AES elasto-mer, a grafting copolymer of poly(styrene-co-acrylonitrile)– SAN and poly(ethylene-co-propylene-co-diene)–EPDMchains. These blends are immiscible and present complexphase behavior. Selective extraction of the blends compo- degree between PS and AES was not high enough toensure the morphological stability against changes duringprocessing in the melting state. The drastic change ofEPDM morphology from continuous to disperse phase hasas consequence a decrease in the intensity of the loss mod-ulus peaks corresponding to the EPDM glass transition.However, the storage modulus at temperatures betweenthe glass transition of EPDM and PS/SAN phases doesnot change significantly. This effect was attributed to thepresence of the SAN rigid chains in the AES.
机译:PS/AES共混物是在AES弹性体存在下原位聚合制备的苯乙烯,AES弹性体是聚(苯乙烯-丙烯腈-丙烯腈)-SAN和聚(乙烯-共丙烯-共二烯)-EPDM链的接枝共聚物。这些混合物是不混溶的,并呈现复相行为。选择性提取 PS 和 AES 之间的混合物成分不够高,无法确保在熔融状态下对加工过程中变化的形态稳定性。三元乙丙(EPDM)形貌从连续相向分散相的剧烈变化导致了三元乙丙玻璃化转变对应的损失模量峰强度的降低。然而,在三元乙丙相和PS/SAN相的玻璃化转变温度下,储能模量没有显著变化。这种影响归因于AES中SAN刚性链的存在。

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