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多层纳米结构可生物降解 PLA/PBSA 薄膜的结构和阻隔性能:强制组装共挤的限制效应。

Structure and Barrier Properties of Multinanolayered Biodegradable PLA/PBSA Films: Confinement Effect via Forced Assembly Coextrusion.

机构信息

Normandie Univ, UNIROUEN Normandie, INSA Rouen, CNRS, PBS, 76000 Rouen, France.

PIMM, Arts et Métiers ParisTech/CNRS/CNAM, 75013 Paris, France.

出版信息

ACS Appl Mater Interfaces. 2017 Aug 30;9(34):29101-29112. doi: 10.1021/acsami.7b08404. Epub 2017 Aug 16.

DOI:10.1021/acsami.7b08404
PMID:28758727
Abstract

Multilayer coextrusion processing was applied to produce 2049-layer film of poly(butylene succinate-co-butylene adipate) (PBSA) confined against poly(lactic acid) (PLA) using forced assembly, where the PBSA layer thickness was about 60 nm. This unique technology allowed to process semicrystalline PBSA as confined polymer and amorphous PLA as confining polymer in a continuous manner. The continuity of PBSA layers within the 80/20 wt % PLA/PBSA layered films was clearly evidenced by atomic force microscopy (AFM). Similar thermal events to the reference films were revealed by thermal studies; indicating no diffusion of polymers during the melt-processing. Mechanical properties were measured for the multilayer film and the obtained results were those expected considering the fraction of each polymer, revealing the absence of delamination in the PLA/PBSA multinanolayer film. The confinement effect induced by PLA led to a slight orientation of the crystals, an increase of the rigid amorphous fraction (RAF) in PBSA with a densification of this fraction without changing film crystallinity. These structural changes allowed to strongly improve the water vapor and gas barrier properties of the PBSA layer into the multilayer film up to two decades in the case of CO gas. By confining the PBSA structure in very thin and continuous layers, it was then possible to improve the barrier performances of a biodegradable system and the resulting barrier properties were successfully correlated to the effect of confinement on the microstructure and the chain segment mobility of the amorphous phase. Such investigation on these multinanolayers of PLA/PBSA with the aim of evidencing relationships between microstructure implying RAF and barrier performances has never been performed yet. Besides, gas and water permeation results have shown that the barrier improvement obtained from the multilayer was mainly due to the reduction of solubility linked to the reduction of the free volume while the tortuosity effect, as usually expected, was not really observed. This work brings new insights in the field of physicochemical behaviors of new multilayer films made of biodegradable polyesters but also in interfacial processes due to the confinement effect induced in these multinanolayer structures obtained by the forced assembly coextrusion. This original coextrusion process was a very advantageous technique to produce eco-friendly materials with functional properties without the help of tie layer, additives, solvents, surface treatments, or inorganic fillers.

摘要

采用多层共挤工艺,通过强制组装将聚丁二酸丁二醇酯-共-己二酸丁二醇酯(PBSA)共挤在聚乳酸(PLA)中,制成 2049 层薄膜,其中 PBSA 层厚约 60nm。这种独特的技术允许以连续的方式将半结晶 PBSA 作为受限聚合物和无定形 PLA 作为限制聚合物进行加工。原子力显微镜(AFM)清楚地证明了 80/20wt%PLA/PBSA 层状薄膜中 PBSA 层的连续性。热研究表明,与参考薄膜具有相似的热事件;表明在熔融加工过程中没有聚合物的扩散。对多层膜进行力学性能测试,得到的结果与每种聚合物的分数相符,表明 PLA/PBSA 多层纳米薄膜无分层。PLA 引起的限制作用导致晶体略有取向,PBSA 中刚性无定形分数(RAF)增加,而该分数的致密化不改变薄膜结晶度。这些结构变化使得 PBSA 层在多层膜中的水蒸气和气体阻隔性能得到了极大的提高,在 CO 气体的情况下,提高了两个数量级。通过将 PBSA 结构限制在非常薄且连续的层中,然后可以提高可生物降解体系的阻隔性能,并且所得阻隔性能成功地与限制对无定形相微观结构和链段迁移率的影响相关。这种对 PLA/PBSA 多层纳米薄膜的研究旨在证明涉及 RAF 和阻隔性能的关系,迄今为止尚未进行过此类研究。此外,气体和水分渗透结果表明,多层膜获得的阻隔性能的提高主要归因于溶解度的降低,这与自由体积的减少有关,而通常预期的迂曲效应并未真正观察到。这项工作为基于可生物降解聚酯的新型多层薄膜的物理化学行为领域以及强制组装共挤获得的这些多层纳米结构中的界面过程带来了新的见解。这种原始的共挤工艺是一种非常有利的技术,可以在无需使用粘结层、添加剂、溶剂、表面处理或无机填料的情况下,生产具有功能特性的环保材料。

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