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Effect of Different Phosphate Glass Compositions on the Process-Induced Macromolecular Dynamics of Polyamide 66

机译:不同磷酸盐玻璃成分对聚酰胺66诱导的大分子动力学的影响

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摘要

The present study provides a fundamental understanding of the mechanism of action of special new phosphate glass (P-glass) systems, having different glass transition temperatures ( ), in polyamide 66 (PA66). Dynamic mechanical analysis (DMA) revealed that the of PA66/low P-glass (ILT-1) was significantly shifted to a lower (65 °C), and another transition appeared at high temperature (166 °C). This was supported by a drop in the melting point and the crystallinity of the PA66/ILT-1 hybrid material as detected by differential scanning calorimetry (DSC). The dielectric spectroscopic investigation on the networks’ molecular level structural variations ( and sub- relaxations) agreed very well with the DMA and DSC findings. Contrary to intermediate (IIT-3) and high P-glass (IHT-1) based materials, the PA66/ILT-1 hybrid material showed an evidence of splitting the PA66 relaxations into two peaks, thus confirming a strong interaction between PA66 and ILT-1 (low P-glass). Nevertheless, the three different P-glass compositions did not show any effect on the PA66 sub- relaxations (related to the –NH and –OH chain end groups’ motion).
机译:本研究对聚酰胺66(PA66)中具有不同玻璃化转变温度()的新型新型磷酸盐玻璃(P-glass)系统的作用机理提供了基本的了解。动态力学分析(DMA)显示,PA66 /低P玻璃(ILT-1)的熔点明显移至较低的温度(65°C),并且在高温(166°C)时出现了另一个转变。如差示扫描量热法(DSC)所检测到的,PA66 / ILT-1杂化材料的熔点和结晶度下降支持了这一点。对网络分子水平结构变化(和亚弛豫)的介电谱研究与DMA和DSC的发现非常吻合。与基于中间(IIT-3)和高P玻璃(IHT-1)的材料相反,PA66 / ILT-1杂化材料显示出将PA66弛豫分为两个峰的证据,从而证实了PA66和ILT之间的强相互作用-1(低P玻璃)。尽管如此,三种不同的P玻璃成分对PA66的亚弛豫没有任何影响(与–NH和–OH链端基的运动有关)。

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