研究马来酸酐接枝乙烯-辛烯共聚物弹性体(POE-g-MAH)和热塑性树脂(PC)协同增韧聚对苯二甲酸丁二酯的脆韧转变,借助扫描电镜(SEM)观察分析增韧体系的相形态和断口形貌,并对增韧机理进行探讨。结果表明,添加PC后,共混体系的脆韧转变在较低POE-g-MAH含量下发生。当PBT与PC质量配比为50/50时,共混物在POE-g-MAH含量为10%时获得超高韧性,达到78kJ/m2,同时拉伸强度达到52.5MPa。SEM分析认为,PC含量较高时,呈现极不规则的近似条状或片状的分散相结构,以及柔性界面层的存在是共混体系在较低弹性体含量下出现脆韧转变而获得高强韧性的主要机制。
Abstract
The brittle-to-ductile transition of poly(butylene terephthalate) synergistically toughened by anhydride grafted poly(ethylene-octene) copolymer elastomer(POE-g-MAH) and thermoplastic resin(PC) was investigated.The morphologies of dispersion phase and fractured surfaces were observed and analyzed with the help of scanning electron microscope(SEM).And the toughening mechanism was also approached.The brittle-to-ductile transition of the blends was observed at a lower POE-g-MAH content for the addition of PC.When POE-g-MAH content was up to 10%,the notched impact strength of the blend with PBT/PC mass ratio of 50/50 was up to 78kJ/m2,with the tensile strength up to 52.5MPa.SEM micrographs showed that the dispersed phase of PC took a very irregular microstructure of slat-like or plate-like shape at higher content of PC.It should be noted that the particular phase morphology of PC covered with a soft layer of POE-g-MAH was the principal mechanisms of strengthening and toughening of the ternary blends.
关键词
聚对苯二甲酸丁二酯 /
POE-g-MAH /
聚碳酸酯 /
脆韧转变 /
微观结构
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Key words
poly(butylene tereph /
POE-g-MAH /
polycarbonate /
brittle-to-ductile t /
microstructure
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脚注
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