材料科学
复合材料
活化能
结晶
聚酰胺
动力学
等温过程
玻璃纤维
纤维
晶体生长
炭黑
Crystal(编程语言)
化学工程
化学
结晶学
热力学
物理化学
工程类
天然橡胶
物理
量子力学
程序设计语言
计算机科学
作者
Yasser Boucenna,Abdelheq Layachi,Abdelhakim Cherfia,Fouad Laoutid,Hamid Satha
出处
期刊:Materials
[Multidisciplinary Digital Publishing Institute]
日期:2023-11-07
卷期号:16 (22): 7073-7073
被引量:13
摘要
This study presents the effect of the addition of 0.4 wt.% carbon black (CB) to polyamide 66 (PA66) containing 30 wt.% short glass fibers (GFs) on the behavior of composite thermal crystallization. Composites were studied by differential scanning calorimetry analysis (DSC) at different cooling rates using wide-angle X-ray scattering (WAXS) and scanning electron microscopy (SEM). This thermal crystallization study highlights the nucleation effect of GFs that promote PA66 crystallization by significantly increasing crystallization kinetics and rates. The activation energies (Eas) calculated by model-free (FWO; KAS) and model-fitting (Kissinger method and C–R method) approaches showed that the combination of both GF and CB decreases the activation energy with respect to neat PA66, meaning that the presence of both additives facilitates crystallization. The Coats–Redfern and Criado methods showed that the crystallization of neat PA66 and related composites follows the second-order reaction, i.e., the decelerated reaction, evidencing compatibility between GFs and the matrix.
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