材料科学
玻璃化转变
聚氨酯
弹性体
无定形固体
退火(玻璃)
微晶
复合材料
猝灭(荧光)
转变温度
大气温度范围
动态力学分析
结晶度
相变
高分子化学
聚合物
热力学
结晶学
化学
荧光
物理
量子力学
超导电性
冶金
作者
K. Hanhi,Bengt Stenberg
标识
DOI:10.1177/026248939301200604
摘要
The results reported indicate that the properties of polyurethanes elastomers can be tailored to serve a wide variety of applications, for low temperature uses as well. The glass transition temperatures of the soft segments (T gs ) which control the low temperature properties of polyurethane elastomers, ranged from -79°C to -27°C (DSC onset values). The transitions observed in the range 75 to 125°C were attributed to hard segment glass transitions. The transitions at temperatures from 140 to 170°C, which were identified especially in the samples of over stoichiometric diisocyanate concentration, evidently arose from the dissociation of allophanate crosslinks and successive ordering processes. The low temperature β” and γ transitions were observed at temperatures from -70°C to -125°C. In addition to the obvious Schatzki crankshaft mechanism, allophanate crosslinking may influence these transitions. Samples that were annealed over the crystal melting temperature and subsequently quenched exhibited higher glass transition temperatures than the samples kept for a long time at room temperature. These results can be explained in terms of better phase separation in annealing and formation of small soft segment crystallites in quenching, in contrast to the formation of large crystalline and amorphous phases in the RT samples.
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