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Study of the addition of poly(ethylene-co-methyl acrylate-co-glycidyl methacrylate) thermoplastic to epoxy resin for use in self-healing composites

机译:将聚(乙烯-丙烯酸甲酯-甲基丙烯酸缩水甘油酯)热塑性塑料添加到环氧树脂中用于自修复复合材料的研究

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摘要

Repair of damaged composite structural elements to restore pristine conditions andmeet regulatory requirements can be a great challenge. Thus, materials capable ofself-healing when damaged are of great interest. In one of the self-healingapproaches studied in the literature, thermoplastic is added to a thermosetting matrixand the damaged material partially recovers its mechanical properties after a healingcycle. This technique employs heat to trigger the healing process and partially reestablishthe mechanical properties of the composite material. In the present study,poly(ethylene-co-methyl acrylate-co-glycidyl methacrylate) (E-MA-GMA)thermoplastic was added to epoxy matrix and evaluated as a self-healing agent. Theinfluence of the type of hardener employed (anhydride or amine) on the properties ofthe material was also investigated. Dynamic mechanical thermal analysis (DMTA)was performed to evaluate changes in viscoelastic properties due to the addition ofthermoplastic. Fourier transform infrared (FTIR) spectroscopy was used to evaluatechemical alterations in thermoplastic-epoxy systems. Atomic force microscopy (AFM)was employed to examine the role of thermoplastic addition on epoxy networkstructure. Healing ability was assessed by comparison of areas damaged byindentations on the surface of samples before and after a healing cycle for materialswith and without E-MA-GMA addition. Results suggest the presence of a E-MA-GMAsecond phase after curing, an increase in glass transition temperature (Tg) for allthermoplastic blended samples as compared to neat epoxy, the presence of onesingle Tg for epoxy anhydride hardened E-MA-GMA mixtures and chemical andstructural alterations on the epoxy network due to addition of E-MA-GMA. Further,the elimination of visible damage areas of the material modified with thermoplasticafter a heating cycle supports the potential use of E-MA-GMA as healing agent.
机译:修复受损的复合结构元件以恢复原始状态和满足法规要求可能是一个巨大的挑战。因此,在损坏时能够自我修复的材料引起了极大的兴趣。在文献中研究的一种自愈方法中,将热塑性塑料添加到热固性基质中,受损材料在愈合周期后部分恢复其机械性能。该技术利用热量来触发愈合过程并部分重建复合材料的机械性能。在本研究中,将聚(乙烯-丙烯酸甲酯-甲基丙烯酸缩水甘油酯)(E-MA-GMA)热塑性塑料添加到环氧基质中,并作为自修复剂进行了评估。还研究了固化剂类型(酸酐或胺)对材料性能的影响。进行了动态机械热分析(DMTA),以评估由于添加了热塑性塑料而引起的粘弹性的变化。傅里叶变换红外(FTIR)光谱用于评估热塑性环氧树脂体系中的化学变化。原子力显微镜(AFM)被用来检查热塑性添加剂对环氧网络结构的作用。通过比较在添加和不添加E-MA-GMA的材料在愈合周期之前和之后样品表面上的压痕所损坏的区域,来评估愈合能力。结果表明,固化后存在E-MA-GMA第二相,与纯环氧树脂相比,热塑性共混样品的玻璃化转变温度(Tg)升高,环氧酸酐硬化的E-MA-GMA混合物中存在单Tg,并且由于添加了E-MA-GMA,导致环氧网络发生化学和结构变化。此外,在加热循环之后消除用热塑性塑料改性的材料的可见损伤区域支持了E-MA-GMA作为治愈剂的潜在用途。

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