期刊论文详细信息
POLYMER 卷:120
Structural evolution from shish-kebab to fibrillar crystals during hot-stretching process of gel spinning ultra-high molecular weight polyethylene fibers obtained from low concentration solution
Article
Wang, Zongbao1  An, Minfang1  Xu, Haojun1  Lv, You1  Tian, Feng2  Gu, Qun3 
[1] Ningbo Univ, Fac Mat Sci & Chem Engn, Ningbo Key Lab Specialty Polymers, Ningbo 315211, Zhejiang, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201204, Peoples R China
[3] Ningbo Univ Technol, Coll Mat Engn, Ningbo 3151006, Zhejiang, Peoples R China
关键词: Ultra-high molecular weight polyethylene;    (UHMWPE) fibers;    Low concentration;    Shish-kebab crystals;    Hot stretching;    Structural evolution;   
DOI  :  10.1016/j.polymer.2017.05.062
来源: Elsevier
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【 摘 要 】

The pre-stretched gel-spinning ultra-high molecular weight polyethylene fibers with low concentration solution obtained from industrial production line were used to study the structural transition from shishkebab to fibrillar crystals during hot-stretching process via in-situ small-angle X-ray scattering, wideangle X-ray diffraction measurements, and scanning electron microscopy. With the increase of hotstretching strain, the kebab crystals (lamellae) undergo stress-induced fragmentation and recrystallization at 90, 100, and 110 degrees C and melting and recrystallization at 120 degrees C to transform to fibrillar crystals. Furthermore, the shish length of pre-stretched fibers at all stretching temperatures first increase and then gradually decrease with the strain, but the number of shish continuously increase and the shish diameter increase firstly and finally keep almost constant. The degree of crystal orientation for all stretching temperatures is as high as above 0.9 during the whole stretching process. These results indicate that the shish-kebab crystals of ultra-high molecular weight polyethylene fibers prepared from low concentration solution can smoothly transform to fibrillar crystals through the hot stretching process. (C) 2017 Published by Elsevier Ltd.

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