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碳纤维增强聚(乙烯-共-甲基丙烯酸)的力学性能

Mechanical Properties of Poly(ethylene-co-methacrylic acid) Reinforced with Carbon Fibers.

作者信息

Haramina Tatjana, Pugar Daniel, Ivančević Darko, Smojver Ivica

机构信息

Faculty of Mechanical Engineering and Naval Architecture, University of Zagreb, I. Lučića 5, 10 000 Zagreb, Croatia.

出版信息

Polymers (Basel). 2021 Jan 5;13(1):165. doi: 10.3390/polym13010165.

Abstract

The capability of poly(ethylene-co-methacrylic acid) (E/MAA) to self-heal is well known, however, its mechanical properties are weak. In this study, composites with single and double layers of unidirectional (UD) carbon fibers were prepared by compression molding. Even a low mass fraction of fibers substantially improved the polymer. The flexural and tensile properties were tested at 0°, 45° and 90° fibers direction and compared to those of the matrix. The mechanical properties in the 0° direction proved superior. Flexural properties depended on the reinforcement distance from the stress neutral plane. The tensile modulus in the 0° direction was 13 times greater despite only a 2.5% mass fraction of fibers. However, both tensile modulus and strength were observed to degrade in the 90° direction. Dynamic mechanical analysis showed the dependence of both structure and properties on the thermal history of E/MAA. Tensile tests after ballistic impact showed that the modulus of the self-healed E/MAA was not affected, yet the strength, yield point, and particularly the elongation at break were reduced. A composite with higher fiber content could be prepared by mixing milled E/MAA particles in fibers prior to compression.

摘要

聚(乙烯 - 共 - 甲基丙烯酸)(E/MAA)的自愈合能力是众所周知的,然而,其机械性能较弱。在本研究中,通过压缩成型制备了具有单层和双层单向(UD)碳纤维的复合材料。即使纤维的质量分数较低,也能显著改善聚合物性能。在纤维方向为0°、45°和90°时测试了弯曲和拉伸性能,并与基体的性能进行了比较。结果表明,在0°方向上的机械性能更优。弯曲性能取决于增强材料与应力中性平面的距离。尽管纤维质量分数仅为2.5%,但在0°方向上的拉伸模量却高出13倍。然而,在90°方向上,拉伸模量和强度均有所下降。动态力学分析表明,E/MAA的结构和性能均取决于其热历史。弹道冲击后的拉伸试验表明,自愈合后的E/MAA模量未受影响,但强度、屈服点,尤其是断裂伸长率有所降低。通过在压缩前将研磨后的E/MAA颗粒与纤维混合,可以制备纤维含量更高的复合材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f36/7794991/ca0275332969/polymers-13-00165-g001.jpg

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