增容
材料科学
极限抗拉强度
艾氏冲击强度试验
复合材料
结晶度
差示扫描量热法
扫描电子显微镜
聚丙烯
热稳定性
马来酸酐
热重分析
聚合物混合物
聚合物
化学工程
共聚物
热力学
物理
工程类
作者
Nora Gharzouli,Rachida Doufnoune,Farid Riahi,Samir Bouchareb
标识
DOI:10.1080/01694243.2018.1539157
摘要
Polypropylene/ethylene-propylene rubber/nanosilica (PP/EPR/nano-SiO2) composites were prepared by a melt blending masterbatch process using a Brabender mixer. In order to improve the interfacial adhesion and achieve diverse desired properties of the composites, nanosilica surface silylation by means of two silane coupling agents: N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane (AEAPTMS) and 3-methacryloxypropyltrimethoxysilane (MPTMS) was explored. The composites were also compatibilized using three compatibilizers: methyl methacrylate grafted PP (MMA-g-PP), glycidylmethacrylate grafted PP (GMA-g-PP) and maleic anhydride grafted PP (MAH-g-PP). The properties of the blends and the composites were examined using tensile and Izod impact tests, differential scanning calorimetry (DSC), thermogravimetric analysis (ATG) and scanning electron microscopy (SEM). According to the mechanical property evaluations, the incorporation of nano-SiO2 particles into PP/EPR blend improved the tensile strength and Young's modulus of the composites. The elongation and Izod impact strength were adversely affected. A significant improvement in the mechanical properties was obtained for the composites with AEAPTMS-SiO2 and MAH-g-PP. The DSC results indicated that the incorporation of the modified silica and MAH-g-PP increased the crystallinity of the composites. However, no significant variation in the crystallinity was observed as a result of the addition of MMA-g-PP and GMA-g-PP. The TGA results revealed that the composites exhibit a higher thermal stability than that of the neat matrix. SEM micrographs of the fractured surfaces revealed a two-phase morphology with EPR nodules being dispersed in the PP matrix. SEM also indicated that the incorporation of MAH-g-PP into PP/EPR composites contributes to a better dispersion of the EPR phase and nano-SiO2 particles in the polymer matrix.
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