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Structural transformation of polyacrylonitrile fibers during stabilization and low temperature carbonization

机译:稳定和低温碳化过程中聚丙烯腈纤维的结构转变

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摘要

The effect of oxidative stabilization and carbonization processes on the structure, mass and mechanical properties of polyacrylonitrile (PAN) precursor fibers was analyzed. A gradual densification of the fibers occurring from mass loss, decrease in fiber diameter and increase in density were observed after stabilization at a maximum temperature of 255 ℃ and carbonization at a maximum temperature of 800 ℃. The tensile strength and modulus of the fibers were found to decrease after stabilization but then increased after low temperature carbonization. The thermal processing of the precursor fibers affected their mode of failure after tensile loading, changing from a ductile type of failure to a brittle type. The type of failure correlated well with the crystal structure changes in the fibers. Whilst the PAN precursor fiber started to exotherm above 225 ℃ in air, no prominent exothermic reaction was measured in the carbonized fibers in air up to 430 ℃. The aromatization index of stabilized fiber was calculated to be ~66%, and that of carbonized fiber was ~99%. FT1R studies indicated that the variation in the chemical structure of the fibers with the stabilization of the fibers. Radial heterogeneity in the stabilized fibers was observed however it was not promoted to the carbonized fibers. Finally, a method to calculate mass retention of PAN precursor fiber after heat treatment was developed, and the calculated percentage mass retained of the precursor fiber after oxidation and carbonization were found to be 81% and 51%, respectively. . This study proposes an effective method to calculate the percentage of mass retained by precursor fibers after stabilization and low temperature carbonization to provide a model for evaluating carbon fiber yield from a given amount of fibers.
机译:分析了氧化稳定和碳化过程对聚丙烯腈(PAN)前体纤维的结构,质量和机械性能的影响。在最高温度为255℃稳定并在最高温度为800℃碳化后,观察到由于质量损失,纤维直径减小和密度增加而引起的纤维逐渐致密化。发现纤维的拉伸强度和模量在稳定后降低,但在低温碳化后增加。前体纤维的热处理会影响其在拉伸载荷后的破坏模式,从韧性破坏类型变为脆性破坏类型。破坏的类型与纤维的晶体结构变化密切相关。 PAN前体纤维在225℃以上的空气中开始放热,而在430℃以下的空气中,碳化纤维中未观察到明显的放热反应。稳定纤维的芳构化指数经计算为〜66%,碳化纤维的芳构化指数为〜99%。 FT1R研究表明,随着纤维的稳定化,纤维化学结构的变化。在稳定的纤维中观察到径向异质性,但是它没有促进碳化纤维。最后,开发了一种计算热处理后PAN前体纤维的质量保留率的方法,发现氧化和碳化后该前体纤维的保留质量百分比分别为81%和51%。 。这项研究提出了一种有效的方法,可以计算稳定化和低温碳化后母体纤维保留的质量百分比,从而为评估给定纤维量的碳纤维收率提供模型。

著录项

  • 来源
    《Polymer Degradation and Stability》 |2016年第6期|39-45|共7页
  • 作者单位

    Carbon Nexus, Institute for Frontier Materials, Deakin University, Geelong, Australia;

    Carbon Nexus, Institute for Frontier Materials, Deakin University, Geelong, Australia;

    Carbon Nexus, Institute for Frontier Materials, Deakin University, Geelong, Australia;

    Carbon Nexus, Institute for Frontier Materials, Deakin University, Geelong, Australia;

    Carbon Nexus, Institute for Frontier Materials, Deakin University, Geelong, Australia;

    Department of Polymer Science and Rubber Technology, Cochin University of Science and Technology, Cochin, India;

    Carbon Nexus, Institute for Frontier Materials, Deakin University, Geelong, Australia;

    Factory of the Future, Swinburne University of Technology, Hawthorn, Australia;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Carbon fibers; Polyacrylonitrile; Stabilization; Carbonization;

    机译:碳纤维;聚丙烯腈稳定;碳化;

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