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Nonisothermal Crystallization Kinetics of Poly(lactic acid) Nucleated with a Multiamide Nucleating Agent

机译:聚酰胺酸成核剂对聚乳酸非等温结晶动力学的影响

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摘要

Addition of a commercial availablemultiamide compound (N, N', N ''-tricyclohexyl-1,3,5-benzenetricarboxylamide, defined here as TMC) into ecofriendly poly(lactic acid) (PLA) can accelerate the crystallization rate of the material remarkably and broaden its applications. In this paper, the nonisothermal crystallization behavior of biodegradable PLA nucleated by 0.3 wt.% of TMC was investigated by differential scanning calorimetry (DSC). The modified Avrami, Tobin, Ozawa, and Mo models were applied to describe the kinetics of the crystallization process. Various parameters of nonisothermal crystallization, such as the crystallization half-time and crystallization rate constant, reflected that TMC significantly accelerated the crystallization process. The activation energy values of the neat PLA and PLA/TMC blend, determined by the Kissinger method, increased with the addition of TMC. The study should be helpful for understanding the relationship between processing and properties of this material.
机译:将市售的多酰胺化合物(N,N',N''-三环己基-1,3,5-苯三羧酰胺,在此定义为TMC)添加到环保的聚乳酸(PLA)中可以显着加快材料的结晶速度并扩大其应用范围。在本文中,通过差示扫描量热法(DSC)研究了以0.3 wt。%TMC成核的可生物降解PLA的非等温结晶行为。修改后的Avrami,Tobin,Ozawa和Mo模型用于描述结晶过程的动力学。非等温结晶的各种参数,如结晶半衰期和结晶速率常数,反映出TMC显着加速了结晶过程。通过基辛格方法确定的纯PLA和PLA / TMC共混物的活化能值随添加TMC而增加。该研究应有助于理解这种材料的加工与性能之间的关系。

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