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聚(L-丙交酯)和聚(L-丙交酯-共-三亚甲基碳酸酯)熔融纺丝纤维:结构-加工-性能关系。

Poly(l-lactide) and Poly(l-lactide- co-trimethylene carbonate) Melt-Spun Fibers: Structure-Processing-Properties Relationship.

机构信息

Department of Fibre and Polymer Technology , KTH Royal Institute of Technology , 100 44 Stockholm , Sweden.

Novus Scientific AB , Virdings allé 2 , 754 50 Uppsala , Sweden.

出版信息

Biomacromolecules. 2019 Mar 11;20(3):1346-1361. doi: 10.1021/acs.biomac.8b01739. Epub 2019 Feb 4.

DOI:10.1021/acs.biomac.8b01739
PMID:30665299
Abstract

l-Lactide/trimethylene carbonate copolymers have been produced as multifilament fibers by high-speed melt-spinning. The relationship existing between the composition, processing parameters and physical properties of the fibers has been disclosed by analyzing how the industrial process induced changes at the macromolecular level, i.e., the chain microstructure and crystallinity development. A poly(l-lactide) and three copolymers having trimethylene carbonate contents of 5, 10 and 18 mol % were synthesized with high molecular weight ( M) up to 377 kDa and narrow dispersity. Their microstructure, crystallinity and thermal properties were dictated by the composition. The spinnability was then assessed for all the as-polymerized materials: four melt-spun multifilament fibers with increasing linear density were collected for each (co)polymer at a fixed take-up speed of 1800 m min varying the mass throughput during the extrusion. A linear correlation resulted between the as-spun fiber properties and the linear density. The as-spun fibers could be further oriented, developing more crystallinity and improving their tensile properties by a second stage of hot-drawing. This ability was dependent on the composition and crystallinity achieved during the melt-spinning and the parameters selected for the hot-drawing, such as temperature, draw ratio and input speed. The crystalline structure evolved to a more stable form, and the degree of crystallinity increased from 0-52% to 25-66%. Values of tensile strength and Young's modulus up to 0.32-0.61 GPa and 4.9-8.4 GPa were respectively achieved.

摘要

聚 L-乳酸/三亚甲基碳酸酯共聚物已通过高速熔融纺丝制成多丝纤维。通过分析工业过程在高分子水平上引起的变化,即链结构和结晶度发展,揭示了纤维的组成、加工参数和物理性能之间的关系。合成了三种具有 5、10 和 18 mol%三亚甲基碳酸酯含量的聚 L-乳酸共聚物,分子量(M)高达 377 kDa,分散度窄。它们的微观结构、结晶度和热性能由组成决定。然后评估了所有聚合材料的可纺性:对于每种(共)聚合物,在固定的收卷速度 1800 m min 下,通过改变挤出过程中的质量流量,收集了四个具有递增线密度的熔融纺多丝纤维。结果表明,初生纤维的性能与线密度之间存在线性相关性。初生纤维可以通过第二阶段的热拉伸进一步取向,从而提高结晶度,改善其拉伸性能。这种能力取决于熔融纺丝过程中实现的组成和结晶度,以及热拉伸过程中选择的参数,如温度、拉伸比和输入速度。结晶结构演变为更稳定的形式,结晶度从 0-52%增加到 25-66%。拉伸强度和杨氏模量分别达到 0.32-0.61 GPa 和 4.9-8.4 GPa。

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