Construction of Interpenetrating Networks Structure in Epoxy Resin With Both High Modulus and High Toughness and Research on Properties of Polymers

IF 2.7 3区 化学 Q2 POLYMER SCIENCE
Xiongfei Zhang, Xiang Shi, Yana Shi, Chunxiao Qu, Qianya Tan
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Abstract

The high-performance development of advanced resin-based composite materials imposes higher demands on the modulus and toughness of epoxy resins. Enhancing the mechanical strength of epoxy resin materials and maintaining their comprehensive performance remain challenging. In recent years, hyperbranched epoxy resins have emerged as an outstanding material for enhancing epoxy resin systems' modulus, toughness, and thermal performance. This study utilizes bisphenol A and trimellitic anhydride as precursors to synthesize a multi-epoxy-terminated hyperbranched epoxy resin through esterification reactions and the incorporation of functional groups. The intermediate terminal carboxylic hyperbranched-modified polyester (TCMP) and the final product high-performance hyperbranched-modified epoxy resin (HP-HMEP) were characterized using FT-IR and 1H NMR spectroscopy, followed by curing with curing agent JH-45. The mechanical and thermal properties of the cured products were subsequently investigated. For the samples cured with JH-45, whose tensile strength, elongation at break, compressive strength, impact strength, and tensile modulus of the E51/HP-HMEP (20 wt%) sample exhibited increases of 51.5%, 44%, 25.5%, 111.6%, and 51.5% compared to those of the E51 samples. Furthermore, the glass transition temperature increases from 67.5°C to 79.3°C, while the initial thermal decomposition temperature rises from 306.9°C to 355.8°C. In summary, the new hyperbranched epoxy resin combines high modulus and high toughness, and the comprehensive performance is significantly improved, which is expected to become an excellent material in the fields of carbon fiber composites, concrete repairation, and so on.

高模高韧性环氧树脂互穿网络结构的构建及聚合物性能研究
先进树脂基复合材料的高性能发展对环氧树脂的模量和韧性提出了更高的要求。提高环氧树脂材料的机械强度和保持其综合性能仍然是一个挑战。近年来,超支化环氧树脂已成为提高环氧树脂体系的模量、韧性和热性能的优秀材料。本研究以双酚A和偏苯三酸酐为前驱体,通过酯化反应和加入官能团合成了端多环氧超支化环氧树脂。采用红外光谱(FT-IR)和核磁共振氢谱(1H NMR)对中间末端羧基超支化改性聚酯(TCMP)和最终产物高性能超支化改性环氧树脂(HP-HMEP)进行表征,并用固化剂JH-45进行固化。随后研究了固化产品的机械和热性能。用JH-45固化后,E51/HP-HMEP (20% wt%)的抗拉强度、断裂伸长率、抗压强度、冲击强度和拉伸模量分别比E51提高了51.5%、44%、25.5%、111.6%和51.5%。玻璃化转变温度从67.5℃上升到79.3℃,初始热分解温度从306.9℃上升到355.8℃。综上所述,新型超支化环氧树脂结合了高模量和高韧性,综合性能显著提高,有望成为碳纤维复合材料、混凝土修复等领域的优良材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Applied Polymer Science
Journal of Applied Polymer Science 化学-高分子科学
CiteScore
5.70
自引率
10.00%
发文量
1280
审稿时长
2.7 months
期刊介绍: The Journal of Applied Polymer Science is the largest peer-reviewed publication in polymers, #3 by total citations, and features results with real-world impact on membranes, polysaccharides, and much more.
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