聚酰胺
结晶度
材料科学
氢键
极限抗拉强度
复合材料
相(物质)
氢
纺纱
粘结强度
化学工程
有机化学
化学
分子
胶粘剂
图层(电子)
工程类
作者
Yufang Li,Danli Nie,Zhining Xiang,Ziqing Cai,Jintao Wang
出处
期刊:Physica Scripta
[IOP Publishing]
日期:2022-08-24
卷期号:97 (10): 105703-105703
被引量:1
标识
DOI:10.1088/1402-4896/ac8c6f
摘要
Abstract During the fiber spinning process, the stretching process is the key to improve the mechanical properties of materials. It is very important to study the effect of hydrogen bond density on the aggregation structure evolution of polyamide for the preparation of high-performance fibers. In this paper, three kinds of polyamides (polyamide 6, polyamide 612 and polyamide 1212) were comparatively studied. In these three polyamides, the hydrogen bond density showed a gradient trend. With the increase of hydrogen bond density, the tensile strength and crystallinity of the materials gradually increased. The phase transition process of the three polyamides had significant difference. This was due to the difference of hydrogen bond density which resulted in different thermally stability of crystal blocks. Finally, the phase evolution schematic of polyamides depending on hydrogen bond density and stretching strains was established.
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