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首页> 外文期刊>New Journal of Chemistry >Miscibility, microstructure, and in situ cure analysis of epoxy-SAN-cloisite 20A nanocomposites
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Miscibility, microstructure, and in situ cure analysis of epoxy-SAN-cloisite 20A nanocomposites

机译:环氧树脂 - SAN-Cloisite 20A纳米复合材料的混溶性,微观结构和原位固化分析

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摘要

Reaction induced phase separation is a characteristic of thermoset/thermoplastic blend systems. Herein, we report the effect of organically modified cloisite 20A nanoclay on the miscibility and curing parameters of an epoxy blend system containing diglycidyl ether of bisphenol A (DGEBA) and poly(styrene-co-acrylonitrile) (SAN) and cured with diamino diphenyl sulphone (DDS). The examined blend compositions were chosen based on the difference in the microstructure. The epoxy/5 phr SAN blend and the epoxy/5 phr SAN/3 wt% cloisite 20A nanocomposite showed a dispered SAN phase in the epoxy matrix. The epoxy/15 phr SAN blend and the epoxy/15 phr SAN/3 wt% cloisite 20A nanocomposite showed a double phase structure. Quantitative analysis of the epoxide conversion during the curing reaction was done by in situ FTIR spectroscopy. The epoxide conversion obeyed first order kinetics in the initial stages of curing. Enhanced viscoelastic effects by the nanoclay decreased the rate of epoxide conversion, which is evident from the in situ cure analysis. Finally, the growth of the complex viscosity during curing was determined by in situ rheometry and theoretically analysed by fitting with the Williams-Landell-Ferry equation. An exponential growth in complex viscosity was observed which was induced by crosslinking. Acceleration of the curing reaction by the nanoclay contributed to the increase in the complex viscosity for the nanocomposites compared to the blends.
机译:反应诱导相分离是热固性/热塑性共混体系的一个特征。在此,我们报告了有机改性cloisite 20A纳米粘土对含有双酚A二缩水甘油醚(DGEBA)和聚(苯乙烯-丙烯腈共聚物)(SAN)并用二氨基二苯砜(DDS)固化的环氧树脂共混体系的相容性和固化参数的影响。根据微观结构的差异选择所检查的共混物成分。环氧树脂/5份SAN共混物和环氧树脂/5份SAN/3 wt%cloisite 20A纳米复合材料在环氧树脂基体中显示分散的SAN相。环氧树脂/15份SAN共混物和环氧树脂/15份SAN/3 wt%cloisite 20A纳米复合材料呈现双相结构。通过原位FTIR光谱对固化反应过程中的环氧化物转化进行了定量分析。在固化初期,环氧化合物的转化遵循一级动力学。原位固化分析表明,纳米粘土增强的粘弹性效应降低了环氧化物转化率。最后,通过现场流变仪测定固化过程中复合粘度的增长,并通过拟合Williams-Landell-Ferry方程进行理论分析。复合粘度呈指数增长,这是由交联引起的。与共混物相比,纳米粘土对固化反应的加速有助于纳米复合材料复合粘度的增加。

著录项

  • 来源
    《New Journal of Chemistry》 |2021年第3期|共9页
  • 作者单位

    Mahatma Gandhi Univ Int &

    Inter Univ Ctr Nanosci &

    Nanotechnol Kottayam 686560 Kerala India;

    Leibniz Inst Polymerforsch Dresden eV Hohe Str 6 D-01069 Dresden Germany;

    Leibniz Inst Polymerforsch Dresden eV Hohe Str 6 D-01069 Dresden Germany;

    Leibniz Inst Polymerforsch Dresden eV Hohe Str 6 D-01069 Dresden Germany;

    Mahatma Gandhi Univ Int &

    Inter Univ Ctr Nanosci &

    Nanotechnol Kottayam 686560 Kerala India;

    Mahatma Gandhi Univ Int &

    Inter Univ Ctr Nanosci &

    Nanotechnol Kottayam 686560 Kerala India;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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