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PE/PE-g-MAH/Org-MMT nanocomposites. II. Nonisothermal crystallization kinetics

机译:PE / PE-g-MAH / Org-MMT纳米复合材料。二。非等温结晶动力学

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The nonisothermal crystallization kinetics of high-density polyethylene (HDPE) and polyethylene (PE)/PE-grafted maleic anhydride (PE-g-MAH)/organic-montmorillonite (Org-MMT) nanocomposite were investigated by differential scanning calorimetry (DSC) at various cooling rates. Avrami analysis modified by Jeziorny, Ozawa analysis, and a method developed by Liu well described the nonisothermal crystallization process of these samples. The difference in the exponent n, m, and a between HDPE and the nanocomposite indicated that nucleation mechanism and dimension of spherulite growth of the nanocomposite were different from that of HDPE to some extent. The values of half-time (t(1/2)), K(T), and F(T) showed that the crystallization rate increased with the increase of cooling rates for HDPE and composite, but the crystallization rate of composite was faster than that of HDPE at a given cooling rate. Moreover, the method proposed by Kissinger was used to evaluate the activation energy of the mentioned samples. It was 223.7 kJ/mol for composite, which was much smaller than that for HDPE (304.6 kJ/mol). Overall, the results indicated that the addition of Org-MMT and PE-g-MAH could accelerate the overall nonisothermal crystallization process of PE. (C) 2004 Wiley Periodicals, Inc. [References: 23]
机译:通过差示扫描量热法(DSC)研究了高密度聚乙烯(HDPE)和聚乙烯(PE)/ PE接枝马来酸酐(PE-g-MAH)/有机蒙脱土(Org-MMT)纳米复合材料的非等温结晶动力学。各种冷却速率。 Jeziorny修改的Avrami分析,Ozawa分析和Liu所开发的方法很好地描述了这些样品的非等温结晶过程。 HDPE与纳米复合材料之间的指数n,m和a的差异表明,纳米复合材料的成核机理和球晶生长尺寸在一定程度上不同于HDPE。半衰期(t(1/2)),K(T)和F(T)的值表明,HDPE和复合材料的结晶速率随冷却速率的增加而增加,但复合材料的结晶速率更快在给定的冷却速率下比HDPE高。此外,基辛格提出的方法被用来评估所述样品的活化能。复合材料为223.7 kJ / mol,远小于HDPE的304.6 kJ / mol。总体而言,结果表明加入Org-MMT和PE-g-MAH可以加速PE的整个非等温结晶过程。 (C)2004 Wiley Periodicals,Inc. [参考:23]

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