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首页> 外文期刊>Journal of Macromolecular Science. Physics >The hexagonal mesophase in atactic polyacrylonitrile: A new interpretation of the phase transitions in the polymer
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The hexagonal mesophase in atactic polyacrylonitrile: A new interpretation of the phase transitions in the polymer

机译:无规聚丙烯腈中的六方中间相:聚合物中相变的新解释

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摘要

When unoriented polyacrylonitrile (PAN) is heated from room temperature, two glass transitions are observed at similar to 100 degreesC and similar to 150 degreesC. Further heating at moderate heating rates, such as 10 degreesC/min, a degradation exotherm is seen at similar to 340 degreesC. But if a very fast heating rate (100 degreesC/min) is used, a melting endotherm can be seen at similar to 320 degreesC before the degradation exotherm. When highly oriented PAN is heated, only a single glass transition is seen at similar to 100 degreesC, whereas the melting/degradation still occurs at similar to 340 degreesC. The X-ray fiber pattern of oriented PAN at room temperature shows just two equatorial peaks (d(1) = 0.525 nm and d(2) = 0.304 nm); any meridional or off-axis scattering is very weak and diffuse. This diffraction pattern remains essentially unchanged until more than 250 degreesC, in the sense that different peaks do not appear or existing peaks disappear. Another surprising and important feature is the existence of a thermoplastic state well below the melting point, which allows the material to be molded into a transparent sheet. Here, a new phase scheme is proposed to interpret the experimental observations on the thermal behaviour of PAN. There are two key ideas: first, there is a thermodynamically stable hexagonal mesophase in PAN; second, unoriented PAN has a two-phase morphology, whereas oriented PAN tends toward a single-phase material. In unoriented samples, there are mesophase and amorphous domains that are both in a glassy state at room temperature. At similar to 100 degreesC, the mesophase glass transforms to the mesophase melt, whereas the amorphous domains become rubbery at about similar to 150 degreesC. In PAN with a single-phase morphology (highly oriented and/or thermally annealed polymer), the amorphous phase is a minor component and hence only a single glass transition at similar to 100 degreesC is observed from the mesophase glass to mesophase melt transformation. The differential scanning calorimeter endotherm at similar to 320 degreesC must be interpreted as the mesophase isotropization temperature. On cooling from the mesophase, PAN does not crystallize because of the lack of stereoregularity, and only a mesophase glass is formed. The mesophase has not been detected in the past because of its extreme viscosity, which means the material does not flow easily. [References: 57]
机译:从室温加热未取向聚丙烯腈(PAN)时,在接近100摄氏度和接近150摄氏度的温度下观察到两个玻璃化转变。在中等加热速率(例如10摄氏度/分钟)下进一步加热,在类似于340摄氏度的条件下观察到降解放热。但是,如果使用非常快的加热速率(100摄氏度/分钟),则在降解放热之前,可以看到类似于320摄氏度的熔融吸热。加热高度取向的PAN时,在类似于100摄氏度的温度下只能看到一个玻璃化转变,而在类似于340摄氏度的温度下仍会发生熔化/降解。室温下定向PAN的X射线纤维图谱仅显示两个赤道峰(d(1)= 0.525 nm和d(2)= 0.304 nm);子午线或轴外的散射都非常微弱且分散。从不出现不同的峰或现有的峰消失的意义上讲,该衍射图样直到250℃以上基本上保持不变。另一个令人惊讶且重要的特征是,其热塑性状态远低于熔点,这使得该材料可以模制成透明片。在这里,提出了一种新的相方案来解释有关PAN热行为的实验观察。有两个关键思想:首先,PAN中存在热力学稳定的六方中间相;第二,未取向的PAN具有两相形态,而取向的PAN倾向于单相材料。在未取向的样品中,存在中间相和无定形域,它们在室温下均呈玻璃态。在接近100摄氏度时,中间相玻璃转变为中间相熔体,而非晶区在大约类似于150摄氏度时变成橡胶状。在具有单相形态(高度取向和/或热退火的聚合物)的PAN中,非晶相是次要成分,因此从中间相玻璃到中间相熔融转变仅观察到类似于100摄氏度的单一玻璃化转变。差示扫描量热仪在类似于320摄氏度的吸热值必须解释为中间相各向同性温度。从中间相冷却时,由于缺乏立构规整度,PAN不会结晶,仅形成中间相玻璃。中间相由于其极高的粘度而在过去未被检测到,这意味着该材料不易流动。 [参考:57]

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