Shape Memory Performance and Microstructural Evolution in PLA/PEG Blends: Role of Plasticizer Content and Molecular Weight.

IF 4.9 3区 工程技术 Q1 POLYMER SCIENCE Polymers Pub Date : 2025-01-17 DOI:10.3390/polym17020225
Jiradet Sringam, Todsapol Kajornprai, Tatiya Trongsatitkul, Nitinat Suppakarn
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Abstract

Poly(lactic acid) (PLA) exhibits excellent shape memory properties but suffers from brittleness and a high glass transition temperature (Tg), limiting its utility in flexible and durable applications. This study explored the modification of PLA properties through the incorporation of poly(ethylene glycol) (PEG), varying in both content (5-20 wt%) and molecular weight (4000-12,000 g/mol), to enhance its suitability for specific applications, such as medical splints. The PLA/PEG blend, containing 15 wt% PEG and with a molecular weight of 12,000 g/mol, exhibited superior shape fixity (99.27%) and recovery (95.77%) in shape memory tests conducted at a programming temperature (Tp) of 45 °C and a recovery temperature (Tr) of 60 °C. Differential scanning calorimetry (DSC) analysis provided insights into the thermal mechanisms driving shape memory behavior of the PLA/PEG blend. The addition of PEG to the PLA blend resulted in a reduction in Tg and an increase in crystallinity, thereby facilitating enhanced chain mobility and structural reorganization. These thermal changes enhanced the shape fixity and recovery of the PLA/PEG blend. Synchrotron wide-angle X-ray scattering (WAXS) was further employed to elucidate the microstructural evolution of PLA/PEG blends during the shape memory process. Upon stretching, the PLA/PEG chains aligned predominantly along the tensile direction, reflecting strain-induced orientation. During recovery, the PLA/PEG chains underwent isotropic relaxation, reorganizing into their original configurations. This structural reorganization highlighted the critical role of chain mobility and alignment in driving the shape memory behavior of PLA/PEG blends, enabling them to effectively return to their initial shape. Mechanical testing confirmed that increasing PEG content and molecular weight enhanced elongation at break and impact strength, balancing flexibility and strength. These findings demonstrated that PLA/PEG blends, especially with 15 wt% PEG at 12,000 g/mol, offer an optimal combination of shape memory performance and mechanical properties, positioning them as promising candidates for customizable and biodegradable medical applications.

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聚乳酸/聚乙二醇共混物的形状记忆性能和微观结构演变:增塑剂含量和分子量的作用。
聚乳酸(PLA)具有优异的形状记忆性能,但其脆性和玻璃化转变温度(Tg)较高,限制了其在柔性和耐用应用中的应用。本研究探索了通过掺入聚乙二醇(PEG)来改性PLA的性能,改变其含量(5- 20wt %)和分子量(4000- 12000 g/mol),以增强其对特定应用的适用性,如医用夹板。在45°C的编程温度(Tp)和60°C的恢复温度(Tr)下进行的形状记忆测试中,聚乙二醇(PEG)含量为15wt %,分子量为12000 g/mol的PLA/PEG共混合物显示出优异的形状固定性(99.27%)和恢复率(95.77%)。差示扫描量热法(DSC)分析揭示了驱动PLA/PEG共混物形状记忆行为的热机制。在PLA共混物中加入PEG导致Tg的降低和结晶度的增加,从而促进了链迁移率和结构重组的增强。这些热变化增强了PLA/PEG共混物的形状固定性和回收率。利用同步加速器广角x射线散射(WAXS)进一步阐明了PLA/PEG共混物在形状记忆过程中的微观结构演变。拉伸后,PLA/PEG链主要沿拉伸方向排列,反映应变诱导的取向。在恢复过程中,PLA/PEG链经历了各向同性弛豫,重组为其原始构型。这种结构重组强调了链迁移率和排列在驱动PLA/PEG共混物形状记忆行为中的关键作用,使它们能够有效地恢复到初始形状。力学测试证实,增加PEG含量和分子量可提高断裂伸长率和冲击强度,平衡柔韧性和强度。这些发现表明,PLA/PEG共混物,特别是在12,000 g/mol时含有15% PEG的PLA/PEG,提供了形状记忆性能和机械性能的最佳组合,使其成为可定制和可生物降解医疗应用的有希望的候选材料。
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来源期刊
Polymers
Polymers POLYMER SCIENCE-
CiteScore
8.00
自引率
16.00%
发文量
4697
审稿时长
1.3 months
期刊介绍: Polymers (ISSN 2073-4360) is an international, open access journal of polymer science. It publishes research papers, short communications and review papers. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Polymers provides an interdisciplinary forum for publishing papers which advance the fields of (i) polymerization methods, (ii) theory, simulation, and modeling, (iii) understanding of new physical phenomena, (iv) advances in characterization techniques, and (v) harnessing of self-assembly and biological strategies for producing complex multifunctional structures.
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