Xin Gao, Xianfeng Wang*, Jianyong Yu, Bin Ding and Xiaohua Zhang*,
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引用次数: 0
Abstract
Electrospun polyacrylonitrile (PAN) nanofibers are widely recognized as precursors for fabricating carbon nanofibers (CNFs), yet the limited degree of cyclization and frequent fiber breakages during stabilization hinder the mechanical performance of the resulting CNFs. This study introduces a strategy to overcome these challenges by synthesizing poly(acrylonitrile-co-acrylic acid) copolymers with controlled acrylic acid ratios. The incorporation of uniformly distributed carboxyl groups in acrylic acid units within the polymer structure enabled an ionic cyclization pathway, reducing the maximum cyclization temperature to 250 °C and achieving a cyclization degree exceeding 82%. This enhanced stabilization process yielded CNFs with highly graphitized structures with an IG/ID ratio of 3.0 and minimal fiber breakages of less than 0.1%. Notably, CNFs derived from P(AN-AA)-5% exhibited a remarkable tensile strength of 28.2 MPa, over three times greater than that of conventional PAN-derived CNFs of 8.8 MPa. This innovative approach highlights the potential of copolymer-based modifications to advance CNF fabrication, offering a pathway for improved mechanical properties and expanded application prospects.
期刊介绍:
ACS Applied Polymer Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics, and biology relevant to applications of polymers.
The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates fundamental knowledge in the areas of materials, engineering, physics, bioscience, polymer science and chemistry into important polymer applications. The journal is specifically interested in work that addresses relationships among structure, processing, morphology, chemistry, properties, and function as well as work that provide insights into mechanisms critical to the performance of the polymer for applications.