混溶性
差示扫描量热法
玻璃化转变
壳聚糖
材料科学
聚合物混合物
高分子化学
放松(心理学)
化学工程
动态力学分析
分析化学(期刊)
聚合物
复合材料
共聚物
热力学
化学
有机化学
工程类
心理学
物理
社会心理学
出处
期刊:Polymer
[Elsevier BV]
日期:2000-09-01
卷期号:41 (19): 7051-7056
被引量:474
标识
DOI:10.1016/s0032-3861(00)00067-7
摘要
There are a few communications concerning the relaxation temperature corresponding to the glass transition temperature of chitosan. We succeeded in observing the Tg of chitosan (to be ca. 203°C) by the direct and careful measurement of differential scanning calorimetry (DSC), which had been assumed not to be sensitive enough to detect it. In addition to this observation, the dynamic mechanical analysis (DMA) measurement in the second heating run showed the α-relaxation at the same temperature as the glass transition temperature observed in DSC. The peak in the tan δ curve appeared at about 150°C in the first heating run as if it were the α-relaxation and might be due to the secondary molecular motion when the chitosan molecules were in the pseudo-stable state. Chitosan was blended with poly(N-vinyl pyrrolidone) in acetic acid solution and this solution was cast to prepare the blend film. The miscibility and the phase structure in the binary blend films were studied using DSC measurements and the wide-angle X-ray diffraction (WAXD) method. The glass transition temperature of the binary blend films decreased with increase of PVP content and the relation obeyed Fox's theory. This implies that the blend system of chitosan and PVP is able to form a miscible phase. It was supported by WAXD observations of the binary blend films.
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