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半结晶聚乙烯的静态和动态特性

Static and Dynamic Properties of Semi-Crystalline Polyethylene.

作者信息

Xu Ming-Ming, Huang Guang-Yan, Feng Shun-Shan, McShane Graham J, Stronge William J

机构信息

State Key Laboratory of Explosion Science and Technology, Beijing Institute of Technology, Beijing 100081, China.

Department of Engineering, University of Cambridge, Cambridge CB2 1PZ, UK.

出版信息

Polymers (Basel). 2016 Mar 28;8(4):77. doi: 10.3390/polym8040077.

DOI:10.3390/polym8040077
PMID:30979202
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6432432/
Abstract

Properties of extruded polymers are strongly affected by molecular structure. For two different semi-crystalline polymers, low-density polyethylene (LDPE) and ultra-high molecular weight polyethylene (UHMWPE), this investigation measures the elastic modulus, plastic flow stress and strain-rate dependence of yield stress. Also, it examines the effect of molecular structure on post-necking tensile fracture. The static and dynamic material tests reveal that extruded UHMWPE has a somewhat larger yield stress and much larger strain to failure than LDPE. For both types of polyethylene, the strain at tensile failure decreases with increasing strain-rate. For strain-rates 0.001⁻3400 s, the yield stress variation is accurately represented by the Cowper⁻Symonds equation. These results indicate that, at high strain rates, UHMWPE is more energy absorbent than LDPE as a result of its long chain molecular structure with few branches.

摘要

挤出聚合物的性能受到分子结构的强烈影响。对于两种不同的半结晶聚合物,即低密度聚乙烯(LDPE)和超高分子量聚乙烯(UHMWPE),本研究测量了弹性模量、塑性流动应力以及屈服应力的应变率依赖性。此外,还研究了分子结构对颈缩后拉伸断裂的影响。静态和动态材料测试表明,挤出的UHMWPE比LDPE具有稍大的屈服应力和大得多的破坏应变。对于这两种类型的聚乙烯,拉伸破坏时的应变均随应变率的增加而降低。对于0.001⁻3400 s的应变率,屈服应力变化可由考珀⁻西蒙兹方程精确表示。这些结果表明,在高应变率下,由于UHMWPE具有少分支的长链分子结构,其比LDPE更能吸收能量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/afbbc8ffd4e6/polymers-08-00077-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/f72c5ebf0da0/polymers-08-00077-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/70a871de2b74/polymers-08-00077-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/11b99b44dd0d/polymers-08-00077-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/369bda1b0f1d/polymers-08-00077-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/903c8cf32dc0/polymers-08-00077-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/5ae40baccb4a/polymers-08-00077-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/3f3d87582f10/polymers-08-00077-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/33ccae0930dc/polymers-08-00077-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/3d7e35c0cb30/polymers-08-00077-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/2b12c7bd55c3/polymers-08-00077-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/afbbc8ffd4e6/polymers-08-00077-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/f72c5ebf0da0/polymers-08-00077-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/ef2b3381a363/polymers-08-00077-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/b57af357d779/polymers-08-00077-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/70a871de2b74/polymers-08-00077-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/11b99b44dd0d/polymers-08-00077-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/369bda1b0f1d/polymers-08-00077-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/903c8cf32dc0/polymers-08-00077-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/5ae40baccb4a/polymers-08-00077-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/3f3d87582f10/polymers-08-00077-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/33ccae0930dc/polymers-08-00077-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/3d7e35c0cb30/polymers-08-00077-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/2b12c7bd55c3/polymers-08-00077-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/6432432/afbbc8ffd4e6/polymers-08-00077-g013.jpg

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