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首页> 外文期刊>Carbohydrate Polymers: Scientific and Technological Aspects of Industrially Important Polysaccharides >Interfacial modification on polyhydroxyalkanoates/starch blend by grafting ?in-situ
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Interfacial modification on polyhydroxyalkanoates/starch blend by grafting ?in-situ

机译:通过嫁接通过嫁接的聚羟基烷烃/淀粉混合物的界面改性?原位

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Highlights ? Interfacial bonding was in situ created by radical grafting leading to smaller adhesion factor. ? Compatibility and interfacial adhesion between PHAs and starch were considerably improved. ? A simple way to make blends with low-cost and good performance was provided. Abstract The interfacial adhesion between polyhydroxyalkanoates (PHAs) and native starch is poor. To improve the interfacial adhesion, PHAs were in-situ grafted onto starch using dicumyl peroxide (DCP) as a free radical initiator. The grafting reaction was carefully characterized and confirmed by gel analysis and Fourier transform infrared spectroscopy (FT-IR). The gel yield of the PHAs/starch/DCP blend increased with the DCP concentration up to 2wt%. Meanwhile, obvious plastic deformation (stretched fibrils) was observed at the interface in the PHAs/starch/DCP blend in comparison with complete interfacial debonding in the PHAs/starch physical blend. The improved interfacial adhesion after grafting was further confirmed by a reduction in adhesion factor (Af ) obtained from dynamic mechanical analysis (DMA). The mechanical strength and the crystallization rate of the PHAs were deteriorated after incorporation of starch, and were backed up by the interfacial improvement. A linear relationship between the mechanical properties and the gel yield was discovered. In addition, the PHAs/starch/DCP blend exhibited higher decomposition active energy (Ea ) and thus better thermal stability in comparison with the PHAs and the PHAs/starch physical blend. Therefore, this study provides a simple route to utilize low-cost starch as a component in biopolymer blend. ]]>
机译:<![cdata [ 突出显示 界面绑定是原位由根本嫁接产生,导致较小的粘附因子。 PHA和淀粉之间的相容性和界面粘附得到大大改善。 提供了一种简单的方法来制作低成本和良好性能的简单方法。 抽象 多羟基烷烃(PHA)和天然淀粉之间的界面粘附性差。为了提高界面粘附,PHA是原位>使用二磺酰基(DCP)作为自由基引发剂接枝到淀粉上。通过凝胶分析和傅里叶变换红外光谱(FT-IR)仔细表征嫁接反应和证实。 PHA /淀粉/ DCP共混物的凝胶产率随高达2 wt%的DCP浓度而增加。同时,在PHA /淀粉/ DCP混合物中的界面中观察到明显的塑料变形(拉伸原纤维),与PHA /淀粉物理混合中的完全界面剥离相比,在PHA /淀粉/ DCP混合物中观察到。通过减少粘合因子( A F ),进一步证实了接枝后的改善的界面粘附。从动态机械获得分析(DMA)。在淀粉掺入后,PHA的机械强度和结晶速率劣化,并通过界面改善来缩短。发现了机械性能与凝胶产率之间的线性关系。此外,PHA /淀粉/ DCP混合物表现出更高的分解活性( E A ),从而更好的热量与PHA和PHA /淀粉物理混合物相比的稳定性。因此,该研究提供了一种简单的途径,以利用低成本淀粉作为生物聚合物混合物中的组分。 ]]>

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