Non-isothermal Crystallization Kinetics of Polyamide 6/Diaminemodified MWNTs Nanocomposite

来源 :Journal of Materials Science & Technology | 被引量 : 0次 | 上传用户:wudajiang1213
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The non-isothermal crystallization kinetics of polyamide 6/diamine-modified multi-walled carbon nanotube (PA6/D-MWNT) nanocomposite was investigated by differential scanning calorimetry (DSC). The modified Avrami equation, the Ozawa equation and the combined Avrami/Ozawa equation were employed to analyze the non-isothermal crystallization data. The crystallization activation energies were also evaluated by the Kissinger method. It was found that the combined Avrami/Ozawa equation could successfully describe the non-isothermal crystallization process. The results showed that D-MWNTs not only acted as effective hetero- geneous nucleating agents for PA6 and noticeably increased the crystallization temperature of PA6, but also influenced the mechanism of nucleation and crystal growth of PA6 and then reduced the overall crystallization rate of the neat PA6 matrix. The crystallization activation energy for the nanocomposite sample was greater than that of the neat PA6, which indicated that the addition of D-MWNTs hindered the mobility of PA6 chain segments. The non-isothermal crystallization kinetics of polyamide 6 / diamine-modified multi-walled carbon nanotube (PA6 / D-MWNT) nanocomposite was investigated by differential scanning calorimetry (DSC). The modified Avrami equation, the Ozawa equation and the combined Avrami / Ozawa equation was employed to analyze the non-isothermal crystallization data. The crystallization was used also also evaluated by the Kissinger method. It was found that the combined Avrami / Ozawa equation could successfully describe the non-isothermal crystallization process. MWNTs not only acted as effective hetero- geneous nucleating agents for PA6 and noticeably increased the crystallization temperature of PA6, but also influenced the mechanism of nucleation and crystal growth of PA6 and then reduced the overall crystallization rate of the neat PA6 matrix. The crystallization activation energy for the nanocomposite sample was greater than that of the neat PA6, which indicates that t he addition of D-MWNTs hindered the mobility of PA6 chain segments.
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