可生物降解聚乳酸基共混膜的机械、屏障和光降解性能

IF 4.9
Ainhoa Fernández-Tena, Jorge L. Olmedo-Martínez, Marcos A. Sabino G., Elizabeth Collinson, Juan V. López, Lourdes Irusta, Alba González, Antxon Martínez de Ilarduya, Gonzalo Guerrica-Echevarria, Nora Aranburu and Alejandro J. Müller
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引用次数: 0

摘要

以聚乳酸(PLA)、聚(ε-己内酯)、(PCL)和增容剂ElvaloyPTW共混物为基材,采用吹膜挤出法制备薄膜;以纯PLA为标准物质。PLA中加入30% PCL导致薄膜的模量、屈服强度和抗撕裂性降低。然而,当ElvaloyPTW加入到70/30 PLA/PCL共混物中时,获得了具有高延展性和改善的气体阻隔性能的薄膜。在氙灯加速条件下,全面研究了PLA/PCL(100/0/0和70/30/0 wt%)和PLA/PCL/c (c =增容剂(ElvaloyPTW), 70/30/3 wt%)共混物吹膜的光降解。采用凝胶渗透色谱(GPC)、1H-NMR、FTIR-ATR、热重分析(TGA)、偏振光光学显微镜(PLOM)和差示扫描量热法(DSC)对光降解样品进行表征。结果表明,PLA/PCL/c薄膜的光降解是通过块体侵蚀机制进行的。这表明,无论聚合物混合物的化学结构和结晶度如何,紫外线穿透样品的强度没有显著降低。PLA和PCL链即使在结晶区域内也容易被光降解;然而,它们在晶体中的光降解性比在非晶态区域的光降解性低。随着光降解时间的延长,其分子量显著降低。FTIR和热分析的综合结果使我们能够确定共混物中的PLA相在PCL和/或PCL/增容剂存在下的降解速度要快得多。最后,光降解作用提高了聚乳酸的结晶速率,影响了聚乳酸球晶的形貌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mechanical, barrier, and photodegradation properties of biodegradable PLA-based blend films

Mechanical, barrier, and photodegradation properties of biodegradable PLA-based blend films

In this work, films based on blends of polylactide (PLA), poly(ε-caprolactone), (PCL), and the compatibilizer ElvaloyPTW were prepared by blown film extrusion; neat PLA was used as a reference material. Adding 30% PCL to PLA resulted in films with decreased modulus, yield strength, and tear resistance. However, when ElvaloyPTW was added to the 70/30 PLA/PCL blend, films featuring high ductility and improved gas barrier properties were achieved. The photodegradation of blown films based on PLA/PCL (100/0/0 and 70/30/0 wt%) and PLA/PCL/c (c = compatibilizer (ElvaloyPTW), 70/30/3 wt%) blends was comprehensively investigated under accelerated conditions using a xenon arc lamp for up to 168 h of UV irradiation. The photo-degraded samples were characterized using gel permeation chromatography (GPC), 1H-NMR, FTIR-ATR, thermogravimetric analysis (TGA), polarized light optical microscopy (PLOM), and differential scanning calorimetry (DSC). The results indicate that the photodegradation of PLA/PCL/c films proceeds via a bulk erosion mechanism. This suggests that UV penetrates the specimens with no significant reduction in intensity, irrespective of the polymer blends' chemical structure and crystallinity. PLA and PCL chains were susceptible to photodegradation even within the crystalline regions; however, their photodegradability was lower in the crystals than in the amorphous regions. A significant decrease in molecular weight was observed with photodegradation time. The combined results of FTIR and thermal analysis allowed us to establish that the PLA phase in the blends experiences a much faster degradation rate in the presence of PCL and/or PCL/compatibilizer. Finally, the effect of photodegradation increased the crystallization rate of PLA and affected the morphology of PLA spherulites.

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