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SEGMENTAL DYNAMICS IN POLYSTYRENE ULTRATHIN FILMS STUDIED BY SINGLE MOLECULE FLUORESCENCE DE-FOCUS MICROSCOPY

机译:单分子荧光脱光显微镜研究的聚苯乙烯超薄膜中的分段动力学

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@@Segmental dynamics of polymers under confinement is a very interesting topic in polymer physics(7, 2). The significance of the researches in this field also lies in the fact that it is related to the fundamental knowledge underlying numerous technologies and applications, such as coating, adhesion, microelectronic industry, nano-fabrication, etc. Polymer films with very small thickness comparable to the polymer chain dimension (for example, the radius of gyration, Rg) offers the ideal model systems for the investigation of confined polymers. According to previous studies(i), systems of this kind exhibit very unique glass transition behavior which is correlated with the segments dynamics directly compared with the bulk states. The most noticeable feature is the shift of glass transition temperature (T_g) compared with the bulk values. Studies show that this behavior may originate from a number of reasons: spatial confinement, free surface effect, polymer-substrate interactions, etc. Although various methods have been employed to explore the physical origins of the shift of T_g under polymers under confinement, unambiguous conclusion is yet not clear.
机译:@@在监禁下的聚合物的节段性动态是聚合物物理学(7,2)中非常有趣的话题。在这一领域的研究的意义还在于一个事实,即它是众多的技术和应用,如涂料,附着力,微电子产业,纳米加工等基本涉及到基础知识的聚合物薄膜具有非常小的厚度相媲美聚合物链尺寸(例如,环状半径,RG)为受限聚合物的研究提供了理想的模型系统。根据以前的研究(I),这种系统的系统表现出非常独特的玻璃转换行为,与散装状态相比,与段动力学相关联。最明显的特征是与散装值相比的玻璃化转变温度(T_G)的偏移。研究表明,这种行为可能来自许多原因:空间限制,自由表面效应,聚合物 - 底物相互作用等。尽管已经采用了各种方法来探索禁闭下的聚合物下T_G的变化的物理起源,但明确的结论尚不清楚。

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