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通过原位形成核壳淀粉基粒子有效增韧聚丙烯。

Effectively toughening polypropylene with in situ formation of core-shell starch-based particles.

机构信息

College of Chemistry and Materials Science, Liaoning Shihua University, Fushun 113001, PR China.

Shenzhen Rayform Technology Co., Ltd., Shenzhen 518131, PR China.

出版信息

Carbohydr Polym. 2020 Dec 1;249:116795. doi: 10.1016/j.carbpol.2020.116795. Epub 2020 Jul 26.

Abstract

Impact modifier particles with the core-shell structure in the polypropylene (PP) matrix were successfully prepared in situ by melt blending PP, thermoplastic starch acetate (TPAS) and poly(ethylene octane) grafted with maleic anhydride (POE-MA). It was found that the core was formed by TPAS, while the shell was formed by POE-MA. This core-shell particle plays an important role in toughening PP. The notched impact strength of PP/TPAS/POE-MA blend was as high as 68.1 KJ/m with an anticipated cost effectiveness. The mechanism of formation of the core-shell starch-based particles could be ascribed to the reactive compatibilization between TPAS and POE-MA which could be confirmed by SEM, and which dramatically improved the mechanical properties of the composites. This provides a new idea for the toughening modification of nonpolar PP, which could widely extend the application of starch and lower the cost.

摘要

在聚丙烯 (PP) 基体中原位成功制备了具有核壳结构的冲击改性粒子,该粒子通过熔融共混 PP、醋酸热塑性淀粉 (TPAS) 和马来酸酐接枝的聚乙烯辛烯 (POE-MA) 制备得到。结果发现,核由 TPAS 形成,而壳由 POE-MA 形成。这种核壳粒子在增韧 PP 中起着重要作用。PP/TPAS/POE-MA 共混物的缺口冲击强度高达 68.1 KJ/m,具有预期的成本效益。核壳淀粉基粒子的形成机制可以归因于 TPAS 和 POE-MA 之间的反应性增容,这可以通过 SEM 得到证实,这极大地提高了复合材料的力学性能。这为非极性 PP 的增韧改性提供了一个新思路,可以广泛扩展淀粉的应用并降低成本。

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