Microstructural evolution and mechanical investigation of hot stretched graphene oxide reinforced polyacrylonitrile nanofiber yarns

• Published in: Polymers for advanced technologies Vol. 31; no. 9; pp. 1935 - 1945
• Main Authors: Yu, Yuxi, Tan, Zekai, Zhang, Jibin, Liu, Guan‐bin
• Format: Journal Article
• Language: English
• Published: Chichester, UK John Wiley & Sons, Ltd 01.09.2020; Wiley Subscription Services, Inc
• Subjects: Alignment; Crystallization; Electrospinning; Fourier transforms; Functional groups; Graphene; graphene oxide; Mechanical properties; Microstructure; nanocomposite; nanofiber yarns; Nanofibers; Polyacrylonitrile; Pyrolysis; Stretching; Strong interactions (field theory); Tensile properties; Yarns
• ISSN: 1042-7147; 1099-1581
• DOI: 10.1002/pat.4918

To reveal the enhancement effect of graphene oxide (GO) in polymer nanofiber yarns, polyacrylonitrile (PAN)/GO nanofibers with different GO content (0.1‐0.5 wt%) were electrospun. The alignment of PAN chains and GO in nanofibers was enhanced by hot stretching of the yarn in dry conditions. The microstructure of the composite nanofiber yarns was investigated through X‐ray diffraction, polarized Fourier transform infrared spectroscopy and transmission electron microscopy. The results demonstrated that the hot stretching above Tg of PAN precursor lead to the increased orientation‐induced crystallization and alignment of PAN chain and GO. The yarn with 0.1 wt% GO and stretched by 4 times its length obtained the highest strength and modules (310.88 ± 24.68 MPa and 7.24 ± 0.55 GPa), which were 600% and 500% higher than those of the as‐electrospun pure PAN yarn. The most promising tensile properties found in hot stretched yarns with low GO content was because the strong interaction occurred between PAN molecules and oxygen‐containing functional groups. Indirect evidence of GO aggregation was also presented, which adversely affected the mechanical properties at higher GO content. Composite nanofiber yarns were sewable and weavable, and could be used as a new generation of composite reinforcement after pyrolysis.