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Morphological interpretations and micromechanical properties of polyamide-6/polypropylene-grafted-maleic anhydrideanoclay ternary nanocomposites

机译:聚酰胺-6 /聚丙烯接枝的马来酸酐/纳米粘土三元纳米复合材料的形态学解释和微机械性能

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摘要

Ternary nanocomposites were fabricated based on an optimized impact modified polyamide-6 (PA-6)/ polypropylene grafted maleic anhydride (PP-g-MA) blend composition with varied concentrations (0-6 wt.% at a step of 2 wt.%) of organoclay, Cloisite 30B?. The morphological attributes such as state of intercalation/exfoliation/crystalline organization and fractured surface topography of the nanocomposites were characterized by transmission electron microscopy (TEM), wide angle X-ray diffraction (WAXD) and scanning electron microscopy (SEM) while the thermal characterizations were done by conducting differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA). The WAXD/DSC studies have revealed that the crystallinity of the nanocomposites remained unaffected. DMA revealed an increase in glass transition temperature (T_g) of the nanocomposites by ~14-19 ℃ relative to the soft polypropylene (PP)-phase, by ~7-12 ℃ relative to the neat matrix PA-6 and by ~4-9 ℃ relative to the optimized impact toughened PA-6 matrix while simultaneously being accompanied by the appearance of a second phase T_g peak progressively at higher temperatures as a function of nanoclay content, indicating the reinforcement effects/restrictions imposed by the nanoclay layers to the polymer chain mobility. The bulk mechanical response of the nanocomposites such as tensile, flexural and impact properties were studied and its related micromechanics aspects have been investigated using composite theories such as Halpin-Tsai, Hui-Shia, Takayanagi and Pukanszky models to analyze the interfacial effects and its role on the stress transfer efficiency. SEM analysis of fractured surface indicated that the failure mode of the nanocomposites undergoes a switch-over from interfacial-effects assisted fibrillation controlled ductile deformation to nanoclay induced soft PP-phase stiffened semi-ductile response via shear-lips formation.
机译:基于优化的抗冲改性的聚酰胺6(PA-6)/聚丙烯接枝的马来酸酐(PP-g-MA)共混物组合物制备三元纳米复合材料,其浓度各不相同(步长为2 wt。%时为0-6 wt。%) )有机粘土,Cloisite 30B?。通过透射电子显微镜(TEM),广角X射线衍射(WAXD)和扫描电子显微镜(SEM)表征了纳米复合材料的形貌属性,例如插层/剥落/晶体组织状态和断裂的表面形貌,同时进行了热表征通过差示扫描量热法(DSC)和动态力学分析(DMA)完成。 WAXD / DSC研究表明,纳米复合材料的结晶度不受影响。 DMA显示,相对于软质聚丙烯(PP)相,纳米复合材料的玻璃化转变温度(T_g)升高了约14-19℃,相对于纯基质PA-6升高了约7-12℃,并且升高了约4-相对于优化的抗冲增韧PA-6基体为9℃,同时伴随着第二相T_g峰的出现,随着纳米粘土含量的增加,第二相T_g逐渐升高,表明纳米粘土层对聚合物产生的增强作用/限制链移动性。研究了纳米复合材料的整体力学响应,例如拉伸,弯曲和冲击性能,并使用诸如Halpin-Tsai,Hui-Shia,Takayanagi和Pukanszky模型的复合理论研究了其相关的微力学方面,以分析界面效应及其作用。关于应力传递效率。断裂表面的SEM分析表明,纳米复合材料的破坏模式经历了从界面效应辅助的原纤化控制的韧性变形到通过剪切唇的形成而引起的纳米粘土引起的软PP相变硬半韧性响应的转变。

著录项

  • 来源
    《Materials & design》 |2010年第10期|P.4693-4703|共11页
  • 作者单位

    Centre for Polymer Science and Engineering, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India;

    Centre for Polymer Science and Engineering, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    polymer matrix composites; mechanical; microstructure;

    机译:聚合物基复合材料;机械;微观结构;

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