4.7 Article

Functional Bionanocomposite Fibers of Chitosan Filled with Cellulose Nanofibers Obtained by Gel Spinning

Journal

POLYMERS
Volume 13, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/polym13101563

Keywords

polymer fiber yarns; bio-nanocomposites; chitosan; cellulose nanofibers; gel; wet spinning; mechanical properties

Funding

  1. Emmy Noether Programme of the German Research Foundation DFG [OS 497/6-1]

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High mechanical performance spun bionanocomposite fibers of chitosan (CHI) filled with cellulose nanofibers (CNFs) were achieved through gel spinning, leading to improved crystallinity and mechanical properties. Increasing the CNF content up to 0.4 wt% in the CHI solution significantly enhanced Young's modulus and tensile strength of the fibers, while further increases in CNF content slightly impacted mechanical parameters due to potential disruption of the CHI matrix hydrogel network. Overall, the addition of 0.4 wt% CNFs into 4 wt% CHI formulations showed optimal compatibility and interface, resulting in bionanocomposite fibers with outstanding mechanical properties.
Extremely high mechanical performance spun bionanocomposite fibers of chitosan (CHI), and cellulose nanofibers (CNFs) were successfully achieved by gel spinning of CHI aqueous viscous formulations filled with CNFs. The microstructural characterization of the fibers by X-ray diffraction revealed the crystallization of the CHI polymer chains into anhydrous chitosan allomorph. The spinning process combining acidic-basic-neutralization-stretching-drying steps allowed obtaining CHI/CNF composite fibers of high crystallinity, with enhanced effect at incorporating the CNFs. Chitosan crystallization seems to be promoted by the presence of cellulose nanofibers, serving as nucleation sites for the growing of CHI crystals. Moreover, the preferential orientation of both CNFs and CHI crystals along the spun fiber direction was revealed in the two-dimensional X-ray diffraction patterns. By increasing the CNF amount up to the optimum concentration of 0.4 wt % in the viscous CHI/CNF collodion, Young's modulus of the spun fibers significantly increased up to 8 GPa. Similarly, the stress at break and the yield stress drastically increased from 115 to 163 MPa, and from 67 to 119 MPa, respectively, by adding only 0.4 wt % of CNFs into a collodion solution containing 4 wt % of chitosan. The toughness of the CHI-based fibers thereby increased from 5 to 9 MJ.m(-3). For higher CNFs contents like 0.5 wt %, the high mechanical performance of the CHI/CNF composite fibers was still observed, but with a slight worsening of the mechanical parameters, which may be related to a minor disruption of the CHI matrix hydrogel network constituting the collodion and gel fiber, as precursor state for the dry fiber formation. Finally, the rheological behavior observed for the different CHI/CNF viscous collodions and the obtained structural, thermal and mechanical properties results revealed an optimum matrix/filler compatibility and interface when adding 0.4 wt % of nanofibrillated cellulose (CNF) into 4 wt % CHI formulations, yielding functional bionanocomposite fibers of outstanding mechanical properties.

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