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Structure and Mechanical Properties of Wet-Spun Fibers Made from Natural Cellulose Nanofibers

机译:天然纤维素纳米纤维制成的湿纺纤维的结构和力学性能

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摘要

Cellulose nanofibers were prepared by TEMPO-mediated oxidation of wood pulp and tunicate cellulose. The cellulose nanofiber suspension in water was spun into an acetone coagulation bath. The spinning rate was varied from 0.1 to 100 m/min to align the nanofibers to the spun fibers. The fibers spun from the wood nanofibers had a hollow structure at spinning rates of >10 m/min, whereas the fibers spun from tunicate nanofibers were porous. Wide-angle X-ray diffraction analysis revealed that the wood and tunicate nanofibers were aligned to the fiber direction of the spun fibers at higher spinning rates. The wood spun fibers at 100 m/min had a Young's modulus of 23.6 GPa, tensile strength of 321 MPa, and elongation at break of 2.2%. The Young's modulus of the wood spun fibers increased with an increase in the spinning rate because of die nanofiber orientation effect.
机译:纤维素纳米纤维是通过TEMPO介导的木浆和被膜化纤维素的氧化制备的。将纤维素纳米纤维在水中的悬浮液旋转到丙酮凝结浴中。纺丝速度在0.1至100 m / min之间变化,以使纳米纤维与纺丝纤维对齐。从木质纳米纤维纺制的纤维具有中空结构,纺丝速率> 10 m / min,而从被膜纳米纤维纺制的纤维是多孔的。广角X射线衍射分析表明,木材和被膜纳米纤维在较高的纺丝速率下与纺丝纤维的纤维方向对齐。 100m / min的木纤维的杨氏模量为23.6GPa,拉伸强度为321MPa,断裂伸长率为2.2%。木材纺丝纤维的杨氏模量由于模头纳米纤维取向效应而随着纺丝速率的增加而增加。

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