首页> 外文会议>SEM IX International Congress on Experimental Mechanics June 5-8, 2000 Orlando, Florida >Nano-mechanical and chemical interrogation of vibrocreep in polymers
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Nano-mechanical and chemical interrogation of vibrocreep in polymers

机译:聚合物中蠕变的纳米力学和化学研究

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摘要

There is considerable evidence that the long-term response of polymers and polymer matrix composites subjected to cyclic loads, stress reversals, or variable cyclic temperatures is characterized by much higher creep rates than those observed from standard laboratory creep experiments. Historically, the understanding and modeling of the interactive mechanisms of creep and cyclic loading effects, defined as vibrocreep, have been inconclusive and present serious challenges. A study of vibrocreep has been initiated which is attempting to describe at the nanometer length scale the effect of the aforementioned factors on the chemical and nanomechanical properties of polymers. We describe the results of detailed analysis of specimens subjected to various loading and temperature histories using Raman spectroscopy and scanning electron and atomic force microscopies. The results show the level of nano-mechanical damage induced by the program loading histories. THese results will be incorporated into a finite element analysis to develop a first generation model for prediction of vibrocreep in polymers.
机译:有大量证据表明,聚合物和聚合物基复合材料承受循环载荷,应力逆转或可变循环温度的长期响应,其蠕变速率要比标准实验室蠕变实验所观察到的蠕变速率高得多。从历史上看,对蠕变和循环荷载作用的相互作用机理(被定义为振动蠕变)的理解和建模一直没有定论,并提出了严峻的挑战。已经开始了对蠕变蠕变的研究,该研究试图在纳米长度尺度上描述上述因素对聚合物的化学和纳米机械性能的影响。我们描述了使用拉曼光谱以及扫描电子和原子力显微镜对经受各种载荷和温度历史的样品进行详细分析的结果。结果显示了程序加载历史记录引起的纳米机械损伤程度。这些结果将被纳入有限元分析中,以开发用于预测聚合物中蠕变蠕变的第一代模型。

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