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Toughening mechanisms in interfacially modified HDPE/thermoplastic starch blends

机译:界面改性HDPE /热塑性淀粉混合物中的增韧机制

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摘要

The mechanical behavior of polymer blends containing 80 wt% of HDPE and 20 wt% of TPS and compatibilized with HDPE-g-MA grafted copolymer was investigated. Unmodified HDPE/TPS blends exhibit high fracture resistance, however, the interfacial modification of those blends by addition of HDPE-g-MA leads to a dramatic drop in fracture resistance. The compatibilization of HDPE/TPS blends increases the surface area of TPS particles by decreasing their size. It was postulated that the addition of HDPE-g-MA induces a reaction between maleic anhydride and hydroxyl groups of the glycerol leading to a decrease of the glycerol content in the TPS phase. This phenomenon increases the stiffness of the modified TPS particles and stiffer TPS particles leading to an important reduction in toughness and plastic deformation, as measured by the EWF method. It is shown that the main toughening mechanism in HDPE/TPS blends is shear-yielding. This article demonstrates that stiff, low diameter TPS particles reduce shear band formation and consequently decrease the resistance to crack propagation.
机译:研究了含有80wt%HDPE和20wt%TP的聚合物共混物的机械性能,并与HDPE-G-MA接枝共聚物进行了相容化。未经修改的HDPE / TPS共混物具有高裂缝性,然而,通过添加HDPE-G-MA对那些共混物的界面改性导致裂缝抗性的显着下降。 HDPE / TPS共混物的相容化通过降低其尺寸来增加TPS颗粒的表面积。假设HDPE-G-MA的加入诱导甘油的马来酸酐和羟基之间的反应,导致TPS相中甘油含量降低。这种现象增加了改性TPS颗粒的刚度,并且通过EWF法测量,导致韧性和塑性变形的重要降低。结果表明,HDPE / TPS共混物中的主要增韧机制是剪切屈服。本文演示了硬度,低直径TPS颗粒减少剪切带形成,从而降低了裂纹繁殖的抗性。

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