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Morphology and mechanical properties of PA12/plasticized starch blends prepared by high-shear extrusion

机译:高剪切挤出制备的PA12 /增塑淀粉共混物的形貌和力学性能

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摘要

PA12/plasticized starch blends (PA12/TPS) were prepared by high-shear twin screw extruder. The morphology development and the mechanical properties of the blends were investigated as a function of the apparent shear rate. High-shear processing has proved to be an efficient method to finely disperse thermoplastic starch in polyamide 12 matrix. Blends containing TPS domains with a size at the nano-scale (R_n ~ 150nm) homogeneously dispersed in PA12 matrix were obtained. From a modeling point of view, the variation of the droplet radius is closer to the Wu's predictions compared to the Serpe's predictions. From the basic hypothesis of these models, it can be then assumed that compatibilization between both phases occurs during the blend processing. Furthermore, this morphology of the blends has been proved to be stable after a reprocessing step in an internal mixer most likely due to either strong hydrogen bonds between the hydroxyl groups of starch and amide groups of polyamide 12 or to potentially cross reactions between macroradicals accounting for in situ formation of graft copolymers with the potential function of compatibilizers. Mechanical properties of the blends were found to be strongly dependent on the shear rate parameter of blend processing as the mechanical properties increase with shear rate. In agreement to the blend morphology, the elongation at break of the blends was greatly improved attesting of a good adhesion between both phases.
机译:通过高剪切双螺杆挤出机制备PA12 /增塑淀粉共混物(PA12 / TPS)。研究了共混物的形态发展和机械性能与表观剪切速率的关系。高剪切加工已被证明是将热塑性淀粉精细分散在聚酰胺12基体中的有效方法。得到了含有TPS结构域的纳米级(R_n〜150nm)尺寸均匀分布在PA12基体中的共混物。从建模的角度来看,与Serpe的预测相比,液滴半径的变化更接近Wu的预测。从这些模型的基本假设出发,可以假设在混合过程中两个阶段之间都出现了相容性。此外,已证明共混物的这种形态在内部混合器中的后处理步骤之后是稳定的,这很可能是由于淀粉的羟基与聚酰胺12的酰胺基团之间存在强氢键,或者是大自由基之间的潜在交叉反应所致。原位形成具有相容剂潜在功能的接枝共聚物。发现共混物的机械性能在很大程度上取决于共混物加工的剪切速率参数,因为机械性能随剪切速率的增加而增加。与共混物形态一致,证明了两相之间的良好粘合性,共混物的断裂伸长率大大提高。

著录项

  • 来源
    《Materials Chemistry and Physics》 |2012年第3期|913-923|共11页
  • 作者单位

    Universite de Lyon, CNRS UMR 5223, Ingenierie des Materiaux Polymeres, Universite Lyon 1, Villeurbanne, F-69622 Lyon, France;

    Universite de Lyon, CNRS UMR 5223, Ingenierie des Materiaux Polymeres, Universite Lyon 1, Villeurbanne, F-69622 Lyon, France;

    MSA de Lyon, CNRS UMR 5223, Ingenierie des Matiriaux Polymeres, Villeurbanne, F-69622 Lyon, France;

    Universite Jean Monnet, CNRS UMR 5223, Ingenierie des Materiaux Polymeres, St Etienne, F-42023, France;

    Universite de Lyon, CNRS UMR 5223, Ingenierie des Materiaux Polymeres, Universite Lyon 1, Villeurbanne, F-69622 Lyon, France;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    polymers; biomaterials; microstructure; mechanical properties;

    机译:聚合物生物材料微观结构机械性能;
  • 入库时间 2022-08-18 00:39:40

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