聚(乳酸)和聚(丁二酸酯)共混物力学性能的测试、表征和建模

IF 4.03
T. Y. Qiu, M. Song, L. G. Zhao
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引用次数: 33

摘要

由于生物可降解聚合物PL(L)A的广泛应用,人们对其力学行为进行了大量的实验和数值研究。然而,PL(L)A的机械脆性或低伸长率极大地限制了它的应用,特别是在生物医学领域。本研究旨在研究以不同重量比与PBS共混提高PLA延展性的潜力。采用HAAKE?高温熔融混合技术,制备了不同重量比的PLA和PBS共混物。Rheomix OS Mixer。采用差示扫描量热法(DSC)研究了共混物的熔融行为、结晶和混相。通过压缩成型生产的小狗骨样品,用于测试单轴拉伸下的力学性能。此外,采用一种具有非线性硬化变量的先进粘塑性模型来模拟PLA/PBS共混物的速率相关塑性变形,并根据拉伸试验数据同步校准模型参数。光学显微镜观察发现,PBS组分有助于聚乳酸的结晶。PLA/PBS共混物的伸长率随PBS含量的增加而增加,但拉伸模量和强度有所降低。应变速率的增加导致应力响应的增强,证明了材料随时间的变形特性。模型模拟的PLA/PBS共混物随时间变化的塑性变形与实验结果吻合较好。PLA/PBS共混物的结晶度随PBS含量的增加而增加。采用机械共混技术与韧性PBS共混可改善纯聚乳酸的脆性,但刚度和强度有所损失。不同应变速率下的拉伸试验证实了共混物的塑性变形随时间的变化,即粘塑性,可以用含非线性硬化变量的Chaboche粘塑性模型进行模拟。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Testing, characterization and modelling of mechanical behaviour of poly (lactic-acid) and poly (butylene succinate) blends

Testing, characterization and modelling of mechanical behaviour of poly (lactic-acid) and poly (butylene succinate) blends

Significant amount of research, both experimental and numerical, has been conducted to study the mechanical behaviour of biodegradable polymer PL(L)A due to its wide range of applications. However, mechanical brittleness or poor elongation of PL(L)A has limited its applications considerably, particularly in the biomedical field. This study aims to study the potential in improving the ductility of PLA by blending with PBS in varied weight ratios.

The preparation of PLA and PBS blends, with various weight ratios, was achieved by melting and mixing technique at high temperature using HAAKE? Rheomix OS Mixer. Differential Scanning Calorimetry (DSC) was applied to investigate the melting behaviour, crystallization and miscibility of the blends. Small dog-bone specimens, produced by compression moulding, were used to test mechanical properties under uniaxial tension. Moreover, an advanced viscoplastic model with nonlinear hardening variables was applied to simulate rate-dependent plastic deformation of PLA/PBS blends, with model parameters calibrated simultaneously against the tensile test data.

Optical Microscopy showed that PBS composition aid with the crystallization of PLA. The elongation of PLA/PBS blends increased with the increase of PBS content, but with a compromise of tensile modulus and strength. An increase of strain rate led to enhanced stress response, demonstrating the time-dependent deformation nature of the material. Model simulations of time-dependent plastic deformation for PLA/PBS blends compared well with experimental results.

The crystallinity of PLA/PBS blends increased with the addition of PBS content. The brittleness of pure PLA can be improved by blending with ductile PBS using mechanical mixing technique, but with a loss of stiffness and strength. The tensile tests at different strain rates confirmed the time-dependent plastic deformation nature of the blends, i.e., viscoplasticity, which can be simulated by the Chaboche viscoplastic model with nonlinear hardening variables.

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