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通过凝胶纺丝法制备的填充有纤维素纳米纤维的壳聚糖功能性生物纳米复合纤维

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

作者信息

Marquez-Bravo Sofia, Doench Ingo, Molina Pamela, Bentley Flor Estefany, Tamo Arnaud Kamdem, Passieux Renaud, Lossada Francisco, David Laurent, Osorio-Madrazo Anayancy

机构信息

Institute of Microsystems Engineering IMTEK, University of Freiburg, 79110 Freiburg, Germany.

Freiburg Materials Research Center FMF, University of Freiburg, 79104 Freiburg, Germany.

出版信息

Polymers (Basel). 2021 May 13;13(10):1563. doi: 10.3390/polym13101563.

Abstract

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. 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.

摘要

通过对填充有纤维素纳米纤维(CNFs)的壳聚糖(CHI)水性粘性配方进行凝胶纺丝,成功制备出了具有极高机械性能的壳聚糖和纤维素纳米复合纺丝纤维。通过X射线衍射对纤维进行微观结构表征,结果显示壳聚糖聚合物链结晶为无水壳聚糖同质异晶体。纺丝过程结合了酸碱中和、拉伸和干燥步骤,从而获得了高结晶度的CHI/CNF复合纤维,且在掺入CNFs时具有增强效果。纤维素纳米纤维的存在似乎促进了壳聚糖的结晶,其作为壳聚糖晶体生长的成核位点。此外,二维X射线衍射图谱显示CNFs和壳聚糖晶体均沿纺丝纤维方向优先取向。在粘性CHI/CNF火棉胶中,将CNF的含量增加至最佳浓度0.4 wt%时,纺丝纤维的杨氏模量显著增加至8 GPa。同样,仅在含有4 wt%壳聚糖的火棉胶溶液中添加0.4 wt%的CNFs,断裂应力和屈服应力分别从115 MPa急剧增加至163 MPa,从67 MPa急剧增加至119 MPa。基于壳聚糖的纤维的韧性由此从5 MJ·m增加至9 MJ·m。对于更高的CNF含量(如0.5 wt%),仍可观察到CHI/CNF复合纤维具有较高的机械性能,但机械参数略有恶化,这可能与构成火棉胶和凝胶纤维(作为干纤维形成的前驱体状态)的壳聚糖基质水凝胶网络的轻微破坏有关。最后,对不同CHI/CNF粘性火棉胶观察到的流变行为以及所获得的结构、热性能和机械性能结果表明,当在4 wt%的CHI配方中添加0.4 wt%的纳米纤维化纤维素(CNF)时,基质/填料具有最佳的相容性和界面,从而得到了具有优异机械性能的功能性生物纳米复合纤维。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d89/8152965/b29a1514d231/polymers-13-01563-g001.jpg

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