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Origins of the two simultaneous mechanisms causing glass transition temperature reductions in high molecular weight freestanding polymer films

机译:导致高分子量独立式聚合物薄膜玻璃化转变温度降低的两种同时机理的起源

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From ellipsometry measurements, Pye and Roth [Phys. Rev. Lett. 107, 235701 (2011)] presented evidence of the presence of two glass transitions originating from two distinctly different and simultaneous mechanisms to reduce the glass transition temperature within freestanding polystyrene films with thickness less than 70 nm. The upper transition temperature T_g~u (h) is higher than the lower transition temperature T_g~l (h) in the ultrathin films. After comparing their data with the findings of others, using the same or different techniques, they concluded that new theoretical interpretation is needed to explain the two transitions and the different dependences of T_g~u (h) and T_g~l (h) on film thickness and molecular weight. We address the problem based on advance in delineating the different viscoelastic mechanisms in the glass-rubber transition zone of polymers. Theoretical considerations as well as experiments have shown in time-scales immediately following the segmental α-relaxation are the sub-Rouse modes with longer length scale but shorter than that of the Rouse modes. The existence of the sub-Rouse modes in various polymers including polystyrene has been repeatedly confirmed by experiments. We show that the sub-Rouse modes can account for the upper transition and the properties observed. The segmental α-relaxation is responsible for the lower transition. This is supported by the fact that the segmental α-relaxation in ultrathin freestanding PS films had been observed by dielectric relaxation measurements and photon correlation spectroscopy. Utilizing the temperature dependence of the segmental relaxation times from these experiments, the glass transition temperature T_g? associated with the segmental relaxation in the ultrathin film is determined. It turns out that T_g? is nearly the same as T_g~l (h) of the lower transition, and hence definitely segmental α-relaxation is the mechanism for the lower transition. Since it is unlikely that the segmental α-relaxation can give rise to two very different transitions simultaneously, a new mechanism for the upper transition is needed, and the sub-Rouse modes provide the mechanism.
机译:根据椭偏测量,Pye和Roth [Phys。牧师107,235701(2011)]提出了两种玻璃化转变的证据,这两种转变来自两种明显不同且同时的机制,它们可以降低厚度小于70 nm的独立式聚苯乙烯薄膜中的玻璃化转变温度。在超薄膜中,上转变温度T_g_u(h)高于下转变温度T_g-1(h)。在使用相同或不同的技术将他们的数据与其他人的发现进行比较之后,他们得出结论,需要新的理论解释来解释电影中T_g〜u(h)和T_g〜l(h)的两个转变和不同的依赖性厚度和分子量。我们在描述聚合物的玻璃-橡胶过渡带中的不同粘弹性机理的基础上解决了该问题。在分段α松弛之后的时间尺度上,理论上的考虑和实验表明,子尺度模式具有更长的长度尺度,但比尺度模式短。实验已经反复证实了亚鲁斯模式在包括聚苯乙烯在内的各种聚合物中的存在。我们表明,子Rouse模式可以解释较高的过渡和观察到的属性。分段α松弛是较低过渡的原因。通过介电弛豫测量和光子相关光谱已经观察到超薄的独立PS膜中的分段α松弛,这一事实得到了支持。利用来自这些实验的分段弛豫时间的温度依赖性,玻璃化转变温度T_g≤100。确定与超薄膜中的节段松弛相关的。原来是T_g?与下过渡的T_g〜l(h)几乎相同,因此,肯定是分段的α松弛是下过渡的机制。由于分段α松弛不太可能同时产生两个非常不同的过渡,因此需要一种用于上过渡的新机制,并且子Rouse模式提供了该机制。

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