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功能梯度碳纳米管增强复合材料板力学行为研究

Investigation of Mechanical Behaviors of Functionally Graded CNT-Reinforced Composite Plates.

作者信息

Cho Jin-Rae, Ahn Young-Ju

机构信息

Department of Naval Architecture and Ocean Engineering, Hongik University, Jochiwon, Sejong 30016, Korea.

Department of Mechanical and Design Engineering, Hongik University, Jochiwon, Sejong 30016, Korea.

出版信息

Polymers (Basel). 2022 Jun 29;14(13):2664. doi: 10.3390/polym14132664.

Abstract

In this paper, the mechanical behavior of a functionally graded carbon nanotube-reinforced composite (FG-CNTRC) plate is numerically investigated. According to the concept of a hierarchical model, the displacement is decomposed into the in-field functions and the assumed thickness-wise monomial. The former is defined on the plate midsurface and is approximated by the 2-D meshfree natural element method (NEM). The FG-CNTRC plate is modeled as a homogenized orthotropic body, and its effective elastic properties are determined by referring to MD simulation and the linear rule of mixtures. Regarding the thickness-wise distribution of CNTs, one uniform and three functionally gradient distributions are taken. Through comparative numerical experiments, the reliability of the numerical method is justified with the maximum relative difference of 6.12%. The effects of the volume fraction and vertical distribution of CNTs, the plate width-thickness and aspect ratios, and the boundary conditions on the bending, free vibration, and buckling behaviors of FG-CNTRC plates are examined. It is found that the mechanical behavior of FG-CNTRC plates is significantly dependent of these major parameters.

摘要

本文对功能梯度碳纳米管增强复合材料(FG-CNTRC)板的力学行为进行了数值研究。根据分层模型的概念,将位移分解为场内函数和假定的沿厚度方向的单项式。前者定义在板的中面上,并通过二维无网格自然单元法(NEM)进行近似。FG-CNTRC板被建模为均匀化的正交各向异性体,其有效弹性性能通过参考分子动力学模拟和线性混合法则来确定。关于碳纳米管的厚度方向分布,采用了一种均匀分布和三种功能梯度分布。通过对比数值实验,数值方法的可靠性得到了验证,最大相对差异为6.12%。研究了碳纳米管的体积分数和垂直分布、板的宽厚比和长宽比以及边界条件对FG-CNTRC板的弯曲、自由振动和屈曲行为的影响。结果发现,FG-CNTRC板的力学行为显著依赖于这些主要参数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a52f/9269440/22dbd56ab81d/polymers-14-02664-g001.jpg

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