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Kinetics of deformation of PTFE at high pressure

机译:高压下PTFE的变形动力学

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摘要

The dependence of the deformation behavior of PTFE on hydrostatic pressure is characterized by determination of the activation volume for plastic flow, V*, which is defined as V*=kT(∂ lnЄ˙/∂ lnσ)T,P(∂ lnσ/∂P)T,Є˙. At a given strain the first partial derivative in this equation, a measure of the strain-rate dependence of the flow stress, is observed to increase with pressure, but at a slower rate than the second partial derivative, a measure of the pressure dependence of the flow stress, decreases with pressure. Hence V* decreases from a value on the order of 300 Å3 at 0.7 kbar to about 160 Å3 at 3.5 kbar and 120 Å3 at 7.59 kbar. The decrease in V* occurs discontinuously near 2.4 kbar and we believe this to be due to a change in the rate-limiting mechanism for deformation. This transition has a marked similarity to that previously observed by the authors in polyethylene; it appears possible that the same deformation mechanisms are operative in both materials.
机译:PTFE变形行为对静水压力的依赖性通过确定塑性流动的活化体积V *来表征,其定义为V * = kT(∂lnЄ˙/∂lnσ)T,P(∂lnσ/∂ P)T,Є˙。在给定应变下,该方程式中的一阶偏导数(即流动应力的应变率相关性的量度)随压力增加而增加,但比二阶导数慢的二阶导数(对流动压力的量度依赖性)慢流动应力随压力降低。因此,V *从0.7 kbar时的300Å3的值减小到3.5 kbar时的约160Å3和7.59 kbar的约120Å3的值。 V *的降低在2.4 kbar附近不连续地发生,我们认为这是由于变形的限速机制发生了变化。这种转变与作者先前在聚乙烯中观察到的明显相似。在两种材料中似乎有可能使用相同的变形机制。

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  • 来源
    《Journal of Applied Physics 》 |1972年第11期| 共9页
  • 作者

    Davis L. A.; Pampillo C. A.;

  • 作者单位

    Materials Research Center, Allied Chemical Corporation, Morristown, New Jersey 07960;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
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