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Elastic properties of thermoplastic elastomers based on poly(tetramethylene oxide) and monodisperse amide segments

机译:基于聚四氢呋喃和单分散酰胺链段的热塑性弹性体的弹性性能

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摘要

The elastic properties of thermoplastic elastomers based on poly(tetramethylene oxide) and monodisperse amide hard segments (HS) were studied in compression and tensile mode as well as with stress relaxation (SR) measurements. For these copolymers the compression set values were low and increased with the modulus and temperature. At low strains (<50%) the tensile set (TS) values were low and the strain recovered almost completely with time. Furthermore, the TS values increased with strain, due to a deformation of the crystallites and a strain hardening of the polyether segments. During the SR measurements, two processes were observed: a fast initial decay in the first 10 s followed by a relaxation process that was dependant on the logarithm of time. The initial decay during the first seconds increased with the modulus of the copolymers and with the applied strain. The SR values for the second process, normalised to the stress at 100 s, were independent of the strain (within the range of 25–300%) and only little dependant on the modulus of the system. In comparison to the literature data the copolymers with the monodisperse HS displayed improved elastic properties and low SR values.
机译:在压缩和拉伸模式以及应力松弛(SR)测量下,研究了基于聚环氧丙烷和单分散酰胺硬链段(HS)的热塑性弹性体的弹性。对于这些共聚物,压缩永久变形值低,并且随模量和温度而增加。在低应变(<50%)时,拉伸永久变形(TS)值低,并且应变随时间几乎完全恢复。此外,由于微晶的变形和聚醚链段的应变硬化,TS值随应变而增加。在SR测量期间,观察到两个过程:在前10 s中快速开始衰减,然后是取决于时间对数的松弛过程。在最初的几秒钟内,初始衰减随共聚物的模量和所施加的应变而增加。第二步的SR值归一化为100 s的应力,与应变无关(在25-300%的范围内),而与系统的模数几乎没有关系。与文献数据相比,具有单分散HS的共聚物显示出改善的弹性性能和较低的SR值。

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