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Effect of filler loading on polymer chain confinement and thermomechanical properties of epoxy/boron nitride (h-BN) nanocomposites

机译:填料载荷对环氧/氮化物(H-BN)纳米复合材料的聚合物链限制和热机械性能的影响

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摘要

This article examines the effect of the addition of hexagonal boron nitride (h-BN) nanopowder on the polymer chain confinement, thermal, morphological and mechanical properties of the epoxy system. A series of epoxy resin/h-BN (EPBN) nanocomposites with varying compositions (0.1, 0.25, 0.5 and 1 wt%) of h-BN was prepared using 4,4 '-diaminodiphenyl sulfone (DDS) as the curing agent. The amount of epoxy chains confined at the h-BN nanofillers was determined and quantified using the results obtained by dynamic mechanical analysis (DMA). h-BN 0.5 wt%/epoxy (EPBN0.5) exhibited the highest volume fraction of the constrained region among the h-BN/epoxy nanocomposites and the presence of h-BN increases the glass transition temperature (T-g) of the epoxy matrix by 10 degrees C. Furthermore, h-BN/epoxy nanocomposites showed a higher storage modulus when compared to the neat epoxy. The incorporation of the h-BN nanopowder into the epoxy system resulted in an excellent improvement in the impact strength and tensile strength of the system, especially with 0.5 wt% h-BN concentration. This could be ascribed to the uniform distribution of the h-BN nanoparticle in the epoxy matrix. Although epoxy nanocomposites exhibited a higher activation energy (which is related to the thermal stability) compared to that of the neat epoxy, thermal analysis revealed that the incorporation of the h-BN nanopowder does not have much influence on the thermal stability of the system. However, fractured surface analysis of the nanocomposites indicated that the surface roughness increases with an increase in h-BN content.
机译:本文研究了六方氮化硼(H-BN)纳米液对环氧系统的聚合物链监禁,热,形态学和力学性能的影响。使用4,4'-二胺二庚烷砜(DDS)作为固化剂,制备具有不同组合物(0.1,0.25,0.5和1wt%)H-Bn的一系列环氧树脂/ H-BN(EPBN)纳米复合材料。使用通过动态机械分析(DMA)获得的结果测定并定量限制在H-BN纳米氧化物的环氧链的量。 H-BN 0.5wt%/环氧(EPBN0.5)在H-BN /环氧纳米复合材料中表现出约束区域的最高体积分数,H-BN的存在增加了环氧基质的玻璃化转变温度(Tg)此外,与整齐的环氧树脂相比,H-BN /环氧纳米复合材料显示出更高的储存量模。将H-BN纳米液掺入环氧系统中导致系统的冲击强度和抗拉强度的显着改善,特别是0.5wt%H-BN浓度。这可以归因于环氧基质中H-BN纳米粒子的均匀分布。尽管与整齐的环氧树脂相比,环氧纳米复合材料表现出较高的活化能量(与热稳定性有关),但热分析显示H-BN纳米液的掺入对系统的热稳定性没有太大影响。然而,纳米复合材料的裂缝表面分析表明表面粗糙度随着H-BN含量的增加而增加。

著录项

  • 来源
    《New Journal of Chemistry》 |2020年第11期|共10页
  • 作者单位

    Mahatma Gandhi Univ Sch Chem Sci Kottayam Kerala India;

    Mahatma Gandhi Univ Sch Chem Sci Kottayam Kerala India;

    Mahatma Gandhi Univ Sch Chem Sci Kottayam Kerala India;

    Mahatma Gandhi Univ Sch Chem Sci Kottayam Kerala India;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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