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Compatibility of Chitosan in Polymer Blends by Chemical Modification of Bio-based Polyesters

机译:通过生物基聚酯的化学改性聚合物共混物中壳聚糖的相容性

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摘要

For some applications of bioplastics like food packaging or medical devices, applying additives can be necessary to avoid microbial activity and hinder biofilm or fouling formation. A currently promising additive is chitosan (CS), the deacetylated form of the biogenic scaffolding material chitin. Due to its hydrophilicity, chitosan is not compatible with most of the thermoplastic bio-based polymers like poly(lactic acid) (PLA) or polyhydroxyalkanoates (PHA). In this work, compatibilization between chitosan and two selected bio-based polyesters, PLA and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), was enhanced by grafting maleic anhydride (MAH) and glycidyl methacrylate (GMA), respectively, onto polymer chains using peroxide. The success of grafting was confirmed via titration methods. The effects of grafting agent and peroxide concentrations on grafting reaction and the physical and thermal properties of the functionalized polyesters were investigated. Compounding of the functionalized polyesters with different weight portions of chitosan was accomplished in a discontinuous internal mixer by in-situ functionalization, followed by blending with chitosan. The titration method, scanning electron microscopy, DSC, FTIR and mechanical characterization of the composites showed good interfacial adhesion and suggest the formation of covalent bonds between functional groups of the polyesters and chitosan, especially for the samples functionalized with GMA. The molecular weights (Mw) of the samples showed a change in the molecular weight related to the thermal degradation of the sample. The Mw of the samples grafted with MAH are lower than those functionalized with GMA. Furthermore, integration of chitosan into non-functionalized PLA polymer matrix showed a nucleating effect, while for PHBV, the increase of crystallinity with the content of chitosan was only observed for grafted PHBV.
机译:对于生物塑料的某些应用(例如食品包装或医疗设备),可能需要使用添加剂以避免微生物活性并阻碍生物膜或结垢的形成。目前最有希望的添加剂是壳聚糖(CS),这是生物支架材料甲壳素的脱乙酰形式。由于其亲水性,壳聚糖与大多数热塑性生物基聚合物(如聚乳酸(PLA)或聚羟基链烷酸酯(PHA))不相容。在这项工作中,分别通过接枝马来酸酐(MAH)和甲基丙烯酸缩水甘油酯(GMA)增强了壳聚糖与两种选定的生物基聚酯PLA和聚(3-羟基丁酸酯-co-3-羟基戊酸酯)(PHBV)之间的相容性使用过氧化物将其连接到聚合物链上。通过滴定法证实了接枝成功。研究了接枝剂和过氧化物的浓度对接枝反应以及功能化聚酯的物理和热性能的影响。通过原位官能化,然后与壳聚糖共混,在不连续的内部混合器中完成具有不同重量份数的壳聚糖的官能化聚酯的混合。复合材料的滴定方法,扫描电子显微镜,DSC,FTIR和机械表征显示出良好的界面粘合性,并表明聚酯和壳聚糖的官能团之间形成了共价键,特别是对于用GMA功能化的样品。样品的分子量(Mw)显示出与样品的热降解有关的分子量变化。用MAH接枝的样品的Mw低于用GMA功能化的样品的Mw。此外,将壳聚糖整合到未官能化的PLA聚合物基质中显示出成核作用,而对于PHBV,仅对于接枝的PHBV观察到结晶度随壳聚糖含量的增加。

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