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首页> 外文期刊>Journal of Macromolecular Science. Physics >Segmental Dynamics in net-poly(methyl methacrylate)-co-poly(n-butyl acrylate) Copolymer Networks
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Segmental Dynamics in net-poly(methyl methacrylate)-co-poly(n-butyl acrylate) Copolymer Networks

机译:净聚(甲基丙烯酸甲酯)-共聚(丙烯酸正丁酯)共聚物网络的分段动力学

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摘要

Dynamic mechanical spectroscopy and differential scanning calorimetry investigations of segmental dynamics are reported for net-poly(methyl methacrylate)-co-poly(n-butyl acrylate) copolymer networks. Three characteristic temperatures, namely, Vogel (T-infinity), glass transition (T-g), and crossover (T-c), were used to define cooperativity range and a new reduced temperature parameter (Solidness, S). The results showed that broadness of the -dispersion (glass transition) and cooperativity length scale at the glass transition temperature decreased with increasing butyl acrylate content and Tg-scaled temperature dependence of the relaxation time (fragility). However, the cooperativity range (T-c-T-infinity), decreased with increasing fragility index. Furthermore, the solidness at T-g (S(T-g)) was nearly independent of chemical structure of the samples. Finally, a correlation was found between two measures of cooperativity length scale in the glass transition region, namely, average volume of cooperatively rearranging regions, V-CRR, and the number of basic units in an act of rearrangement in the glass transition region, Z(T-g), determined from two completely independent experimental techniques.
机译:报道了净-聚(甲基丙烯酸甲酯)-共聚(丙烯酸正丁酯)共聚物网络的动态力学光谱学和差示扫描量热法对节段动力学的研究。使用三个特征温度,即Vogel(T-无穷大),玻璃化转变(T-g)和交叉(T-c),定义了协同作用范围和一个新的降低的温度参数(Solidness,S)。结果表明,随着丙烯酸丁酯含量的增加和弛豫时间(脆性)的Tg标度温度依赖性,在玻璃化转变温度下-分散(玻璃化转变)的宽度和协同长度尺度降低。但是,随着脆性指数的增加,协同范围(T-c-T-无穷大)减小。此外,在T-g(S(T-g))时的硬度几乎与样品的化学结构无关。最后,在玻璃化转变区域的两个协作长度尺度的度量之间找到了相关性,即协同重排区域的平均体积V-CRR和玻璃化转变区域Z的重排行为中基本单位的数量Z (Tg)由两种完全独立的实验技术确定。

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