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首页> 外文期刊>Biomacromolecules >Nanoamphiphilic Chitosan Dispersed Poly(lactic acid) Bionanocomposite Films with Improved Thermal, Mechanical, and Gas Barrier Properties
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Nanoamphiphilic Chitosan Dispersed Poly(lactic acid) Bionanocomposite Films with Improved Thermal, Mechanical, and Gas Barrier Properties

机译:具有改善的热,机械和气体阻隔性能的纳米两亲性壳聚糖分散聚乳酸复合膜

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This article demonstrates the synthesis of lactic acid oligomer-grafted-chitosan (OLLA-g-CH), a nanoamphiphilic molecule, by in situ condensation polymerization and its effective use as a nanofiller for improvement in multiple properties of poly(lactic acid) (PLA) films, essential for stringent food packaging applications. Fourier transform infrared spectroscopy (FTIR) analysis shows the presence of amide-ester bond at 1539 cm(-1), which confirms the structural grafting of OLLA chains with chitosan molecules. This nanoamphiphilic OLLA-g-CH molecule act as surfactant containing hydrophilic chitosan head and hydrophobic OLLA tails with average size in the range of similar to 2-4 nm. Prepared PLA/OLLA-g-CH bionanocomposite films appear with uniform dispersion of nanoamphiphilic OLLA-g-CH molecules with self assembled micelles having size as low as similar to 20 nm and as high as similar to 150 nm with core-shell morphology in PLA matrix. This nanofiller is found very effective toward significant reduction in oxygen permeability (OP) by similar to 10-fold due to the reduction in solubility of oxygen molecules and improvement in crystal nucleation density due to availability of nanonucleating sites. Ultimate tensile strength (UTS) of PLA/OLLA-g-CH bionanocomposite films are relatively comparable to that of PLA, however, elongation at break is improved significantly. The onset of thermal degradation of PLA/(OLLA-g-CH) films is also found comparable to that of PLA film. The glass transition temperature (T-g) of bionanocomposites is decreased by more than 18 degrees C with increase in OLLA-g-CH loading, which indicates the improved plasticization characteristics of PLA matrix. The crystallization kinetics suggest nonthree dimensional truncated spherical structures, which is controlled by the combination of thermal and athermal instantaneous nucleations. POM analysis suggested that the spherulite growth of PLA is improved significantly with the addition of OLLA-g-CH. The reduction in T-g of PLA with improvement in elongation at break and multifold reduction in oxygen permeability offers this bionanocomposite films, a promising candidate for stringent food packaging applications.
机译:本文展示了通过原位缩聚反应合成纳米两亲性分子的乳酸低聚物接枝壳聚糖(OLLA-g-CH)以及将其有效用作改善聚乳酸(PLA)多种性能的纳米填料的方法)薄膜,对于严格的食品包装应用至关重要。傅里叶变换红外光谱(FTIR)分析显示在1539 cm(-1)处存在酰胺-酯键,这证实了壳聚糖分子对OLLA链的结构接枝。该纳米两亲性OLLA-g-CH分子充当表面活性剂,其包含亲水壳聚糖头部和疏水性OLLA尾部,其平均大小在2-4nm的范围内。制备的PLA / OLLA-g-CH纳米复合材料薄膜具有均匀的纳米两亲性OLLA-g-CH分子分散体,其自组装胶束的尺寸低至20 nm,高至150 nm,且在PLA中具有核-壳形态矩阵。由于氧分子的溶解度降低和由于纳米核位点的可用性而提高了晶体成核密度,发现该纳米填料非常有效地使氧渗透率(OP)显着降低约10倍。 PLA / OLLA-g-CH纳米复合材料薄膜的极限拉伸强度(UTS)与PLA相当,但是断裂伸长率得到了显着提高。还发现PLA /(OLLA-g-CH)薄膜的热降解开始时间与PLA薄膜相当。随着OLLA-g-CH负载量的增加,生物纳米复合材料的玻璃化转变温度(T-g)降低了18摄氏度以上,这表明PLA基质的塑化特性得到了改善。结晶动力学表明无三维截断的球形结构,这由热和非热瞬时成核的组合来控制。 POM分析表明,添加OLLA-g-CH可显着改善PLA的球晶生长。这种Pion的T-g降低,断裂伸长率的提高和透氧率的多次降低提供了这种仿生复合膜,是严格的食品包装应用的有希望的候选者。

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