Molecular Mobility in the Amorphous Phase Determines the Critical Strain of Fibrillation in the Tensile Stretching of Polyethylene
Molecular Mobility in the Amorphous Phase Determines the Critical Strain of Fibrillation in the Tensile Stretching of Polyethylene
复制标题
非晶相中的分子迁移率决定了聚乙烯拉伸拉伸中原纤化的临界应变
DOI:
10.1007/s10118-020-2362-5
复制
发表时间:
2019-11-27
影响因子:
4.3
通讯作者:
Jiang, Zhi-Yong
中科院分区:
文献类型:
--
作者:
Li, Rui;Yang, Guo-Xing;Jiang, Zhi-Yong
The microstructural development of bimodal high density polyethylene subjected to tensile deformation was investigated as a function of strain after annealing at different temperatures by means of a scanning synchrotron small angle X-ray scattering (SAXS) technique. Two different deformation mechanisms were activated in sequence upon tensile deformation: intralamellar slipping of crystalline blocks dominates the deformation behavior at small deformations whereas a stress-induced crystalline block fragmentation and recrystallization process occurs at a critical strain yielding new crystallites with the molecular chains preferentially oriented along the drawing direction. The critical strain associated with the lamellar-to-fibrillar transition was found to beca.0.9 in bimodal sample, which is significantly larger than that observed for unimodal high-density polyethylene (0.4). This observation is primarily due to the fact that the bimodal sample possesses a greater mobility of the amorphous phase and thereby a reduced modulus of the entangled amorphous network. The conclusion of the mobility of the amorphous phase as a determining factor for the critical strain was further proven by the1H-NMRT2relaxation time. All these findings contribute to our understanding of the excellent slow crack growth resistance of bimodal polyethylene for pipe application.