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The role of the amorphous phase in the re-crystallization process of cold-crystallized poly(ethylene terephthalate)

机译:非晶相在冷结晶聚对苯二甲酸乙二酯的重结晶过程中的作用

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The process of re-crystallization in poly(ethylene terephthalate) is studied by means of X-ray diffraction (SAXS and WAXS) and dynamical mechanical thermal analysis. Samples cold-crystallized for 9 h at the temperatures T-c = 100 degrees C and T-c = 160 degrees C, i.e. in the middle of the alpha relaxation region and close to its upper bound, respectively, are analyzed. During heating from room temperature, a structural rearrangement of the stacks is always found at T-r similar or equal to T-c + 20 degrees C. This process is characterized by a decrease of the linear crystallinity, irrespective of T-c; on the other hand, the WAXS crystallinity never increases with T below T-c + 30 degrees C. The lamellar thickness in the low-T-c sample decreases significantly after the structural transition, whereas in the high-T-c sample the lamellar thickness remains almost unchanged. In both, high- and low-T-c, the interlamellar thickness increases above T-r. Moreover, the high-T-c sample shows a lower rate of decrease of the mechanical performance with increasing T as the threshold T-r is crossed. This result is interpreted in terms of the formation of rigid amorphous domains where the chains are partially oriented. The presence of these domains would determine i) the stabilization of the crystalline lamellae from the thermodynamic point of view and ii) the increase of the elastic modulus of the amorphous interlamellar regions. This idea is discussed by resorting to a phase diagram. An estimation of the chemical-potential increase of the interlamellar amorphous regions, due to the enhancement of the structural constraints hindering segmental mobility, is offered. Finally, previous calculations developed within the framework of the Gaussian chain model (F.J. Balta Calleja et al., Phys. Rev. B 75, 224201 (2007)) are used here to estimate the degree of chain orientation induced by the structural transition of the stacks.
机译:通过X射线衍射(SAXS和WAXS)和动态机械热分析,研究了聚对苯二甲酸乙二醇酯中的重结晶过程。分析了在T-c = 100摄氏度和T-c = 160摄氏度,即分别在α弛豫区的中部和接近其上限的情况下冷结晶9小时的样品。在从室温加热的过程中,总是在类似或等于T-c + 20摄氏度的T-r处发现电池堆的结构重排。此过程的特征是线性结晶度降低,而与T-c无关。另一方面,当T低于T-c + 30摄氏度时,WAXS结晶度不会增加。低T-c样品中的层状厚度在结构转变后显着降低,而在高T-c样品中,层状厚度几乎保持不变。在高T-c和低T-c中,层间厚度都增加到T-r以上。此外,随着阈值T-r的增加,高T-c样品的机械性能下降率随T的增加而降低。根据链部分取向的刚性非晶域的形成来解释该结果。这些域的存在将决定i)从热力学观点来看晶体薄片的稳定性,以及ii)无定形层间区域的弹性模量的增加。通过求助于相图来讨论这个想法。提供了一种对层间非晶区域化学势增加的估计,这是由于阻碍片段迁移的结构约束的增强所致。最后,在此之前在高斯链模型框架内开发的计算方法(FJ Balta Calleja等人,Phys。Rev. B 75,224201(2007))在这里用于估计由链的结构转变引起的链取向程度。堆栈。

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