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Properties and morphology of interpenetrating polymer networks based on poly(urethane-imide) and epoxy resin

机译:聚氨基甲酸酯与环氧树脂互穿的聚合物网络的形貌

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摘要

Incorporating elastic polyurethane in epoxy resin (EP) can enhance the physico-chemical properties but deteriorate the thermal stability. Poly(urethane-imide) (PUI) with a high reactive function group (-NCO), which combines the advantages of polyurethane and polyimide, was synthesized to simultaneously improve the toughness and thermal stability of epoxy resin. EP/PUI composites were prepared based on epoxy resin and poly(urethaneimide) with 4,4-diaminodiphenylmethane as the curing agent using a simultaneous polymerization method. FTIR analysis confirmed the formation of EP-g-PUI interpenetrating polymer networks via a reaction between -NCO of poly(urethane-imide) and -OH of epoxy resin. The thermal stability and mechanical properties were examined by thermogravimetric analysis (TGA), dynamic mechanical analysis (DMA) and stress-tensile method, respectively. Corresponding to the pure epoxy resin, which has three stage thermal decomposition, the resulting PUI/EP composite exhibits only one stage and has a much higher initial decomposition temperature (323.8°C) than that (189.8°C) of the epoxy resin. Moreover, the EP/PUI composite has a higher glass transition temperature, tensile strength and breaking elongation when 30 phr PUI was added. With increasing PUI content to 70 phr, the breaking elongation was 213 times higher than that of the neat epoxy resin. The morphology of these composites was also investigated further by scanning electronic microscopy (SEM) and transmission electron microscopy (TEM). The results showed that a grafted interpenetrating polymer network was formed.
机译:在环氧树脂(EP)中掺入弹性聚氨酯可以增强物理化学性质,但会降低热稳定性。合成了具有高反应活性官能团(-NCO)的聚氨基甲酸酯(PUI),它结合了聚氨酯和聚酰亚胺的优点,同时提高了环氧树脂的韧性和热稳定性。采用同时聚合的方法,以4,4-二氨基二苯甲烷为固化剂,以环氧树脂和聚氨基甲酸酯为基础,制备了EP / PUI复合材料。 FTIR分析证实了通过聚(氨基甲酸酯-酰亚胺)的-NCO和环氧树脂的-OH之间的反应形成了EP-g-PUI互穿聚合物网络。分别通过热重分析(TGA),动态力学分析(DMA)和应力拉伸方法检查了热稳定性和机械性能。对应于具有三阶段热分解的纯环氧树脂,所得的PUI / EP复合材料仅表现出一个阶段,并且具有比环氧树脂的初始分解温度(189.8°C)高得多的初始分解温度(323.8°C)。此外,当添加30 phr PUI时,EP / PUI复合材料具有更高的玻璃化转变温度,拉伸强度和断裂伸长率。随着PUI含量增加到70 phr,断裂伸长率是纯环氧树脂的213倍。还通过扫描电子显微镜(SEM)和透射电子显微镜(TEM)进一步研究了这些复合材料的形态。结果表明,形成了接枝互穿的聚合物网络。

著录项

  • 来源
    《Macromolecular Research》 |2010年第10期|p.944-950|共7页
  • 作者单位

    State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing, 100029, China;

    State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing, 100029, China;

    State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing, 100029, China;

    State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing, 100029, China;

    Key Laboratory on Preparation and Processing of Novel Polymer Materials of Beijing, Beijing, 100029, China;

    State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing, 100029, China;

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

    poly(urethane-imide); epoxy resin; thermal stability; morphology; interpenetrating polymer networks;

    机译:聚酰亚胺;环氧树脂;热稳定性;形貌;互穿聚合物网络;

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