通过在碳纤维生产中产生氧浓度梯度来改性聚丙烯腈纤维的加速热稳定

E. A. Trofimenko, T. V. Bukharkina, S. V. Verzhichinskaya
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摘要

目标。这项工作旨在改进用于生产高强度碳纤维的聚丙烯腈(PAN)纤维的加速热稳定技术,通过减少异相核壳结构的形成,在热处理炉中产生氧浓度梯度,同时保持总热稳定时间为30分钟。优化的工艺条件导致了更温和的热稳定条件。与先前开发的加速热稳定技术相比,降低了最终热处理温度和热稳定区之间的温差,同时保持了目标体积密度参数。在实验碳纤维生产线上,对工业生产的12S前驱体在不同条件下的热稳定性进行了研究,包括测量体积密度,用差示扫描量热法(DSC)分析氧化反应的热效应,并对所得样品的显微照片进行了研究。采用选定的组分,在4个稳定区确定了PAN纤维热稳定的最佳工艺。在一定时间内(30min)达到稳定聚合物纤维的目标体积密度和DSC热氧化反应效果时,核壳结构的形成明显减少。由此产生的技术体系有望以较低的成本生产高强度(4.5 GPa, 4.9 GPa) PAN纤维。在将PAN的总热稳定时间保持在30分钟水平的同时,这比使用的工业工艺少了三倍,可以减少异相结构的形成,降低最终加工温度,缩小稳定区之间的温差。这对工业过程的稳定性和安全性以及确保所获得产品的质量产生了积极影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modification of accelerated thermal stabilization of polyacrylonitrile fibers by creating an oxygen concentration gradient in the production of carbon fiber
Objectives. The work set out to modify the technology of accelerated thermal stabilization of polyacrylonitrile (PAN) fibers used in the production of high-strength carbon fibers by reducing the formation of a heterophase core–shell structure to create an oxygen concentration gradient in heat treatment furnaces while maintaining a total thermal stabilization time of 30 min. The optimized process conditions led to milder thermal stabilization conditions, reducing both the final heat treatment temperature and the temperature difference between the thermal stabilization zones while simultaneously maintaining the target volume density parameter with respect to the previously developed accelerated thermal stabilization technology.Methods. The thermal stabilization study of an industrially produced 12S precursor under different conditions on an experimental carbon fiber production line included measurement of bulk density, analysis of the thermal effects of the oxidation reaction by differential scanning calorimetry (DSC), and a study of micrographs of the resulting samples.Results. The optimum process of thermal stabilization of PAN fiber was determined in four stabilization zones using selected compositions. The formation of the core–shell structure is significantly reduced when the target volume density and DSC thermal oxidation reaction effect of the stabilized polymer fiber are achieved in a given time (30 min).Conclusions. The resulting technology regime is promising for the production of high strength (4.5 GPa, 4.9 GPa) PAN fibers at a reduced cost. While maintaining the total thermal stabilization time of PAN at the level of 30 min, which is three times less than the industrial processes used, it was possible to reduce the formation of a heterophase structure, as well as lowering the final processing temperature and reducing the temperature difference between the stabilization zones. This is promising in terms of a positive effect on the stability and safety of the industrial process, as well as ensuring the quality of the obtained products.
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