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Wear resistant all-PE single-component composites via 1D nanostructure formation during melt processing.

Authors :
Hees, Timo
Zhong, Fan
Koplin, Christof
Jaeger, Raimund
Mülhaupt, Rolf
Source :
Polymer. Aug2018, Vol. 151, p47-55. 9p.
Publication Year :
2018

Abstract

Melt-flow-induced crystallization of polyethylene blends having tailored ultrabroad molar mass distribution affords extended-chain ultrahigh molar mass (UHMWPE) nanophases resembling nanofibers which effectively reinforce the polyethylene matrix. Unparalleled by state-of-the-art high density polyethylene (HDPE), the resulting melt-processable “all-polyethylene” single component composites exhibit simultaneously improved wear resistance, toughness, stiffness and strength. Key intermediates are trimodal blends prepared by melt compounding HDPE with bimodal UHMWPE/HDPE wax reactor blends (RB) readily tailored by ethylene polymerization on supported two-site catalysts. Whereas HDPE wax, varied up to 54 wt.-%, serves as processing aid lowering melt viscosity, UHMWPE varied up to 63 wt.-% accounts for improved blend properties. UHMWPE platelet-like nanophase separate during ethylene polymerization and readily melt during injection molding of RB/HDPE blends producing extended-chain fiber-like UHMWPE nanostructures of 100 nm diameter as shish which nucleate HDPE and HDPE wax crystallization to form shish-kebab-like structures. At 32 wt.-% UHMWPE content shish-kebab-like reinforcing phases account for massive polyethylene self-reinforcement as reflected by improved Young's modulus (+420%), tensile strength (+740%) and notched Izod impact strength (+650%) without impairing HDPE injection molding. All-PE composites exhibit high wear resistance entering ranges typical for polyamide and monomodal UHMWPE which is not processable by injection molding under identical conditions. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00323861
Volume :
151
Database :
Academic Search Index
Journal :
Polymer
Publication Type :
Academic Journal
Accession number :
131355739
Full Text :
https://doi.org/10.1016/j.polymer.2018.07.057