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Drawing behavior and mechanical properties of ultra-high molecular weight polyethylene blends with a linear polyethylene wax
Ultra-high molecular weight polyethylene (UHMWPE; Mw = 103 kg/mol) is blended with a low molecular weight, linear polyethylene (PEwax; Mw = 1 kg/mol) and the solid state drawing behavior and mechanical properties are explored. The results indicate that the low molecular weight polyethylene wax acts...
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Published in: | Polymer (Guilford) 2018-09, Vol.153, p.354-361 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Ultra-high molecular weight polyethylene (UHMWPE; Mw = 103 kg/mol) is blended with a low molecular weight, linear polyethylene (PEwax; Mw = 1 kg/mol) and the solid state drawing behavior and mechanical properties are explored. The results indicate that the low molecular weight polyethylene wax acts as a solvent for the UHMWPE which leads to an improvement in rheological properties and the maximum attainable draw ratio of the blends. The maximum attainable Young's modulus of the drawn films increases with more than a factor 2 without removal of the solvent. Moreover, it is found that the maximum attainable tensile strength of the drawn blends also increases significantly from ∼1 GPa to ∼1.5 GPa upon addition of 60 wt% of the PEwax. Based on these results, a new route is proposed for the processing of highly oriented polyethylene, which has certain characteristics in common with both melt spinning and solution spinning but, in fact, is neither of the two.
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•UHMWPE is melt blended with a low molecular weight polyethylene wax at various weight fractions.•Low molecular weight polyethylene wax acts like solvent for the UHMWPE.•Rheological properties and solid-state drawability of the UHMWPE blends are significantly improved.•The drawn UHMWPE blends possess enhanced mechanical properties without removal of the solvent. |
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ISSN: | 0032-3861 1873-2291 |
DOI: | 10.1016/j.polymer.2018.01.083 |