Journal of Polymer Science · 2020 · 14 citations · 47 references
Natural SciencesMaterials EngineeringMaterials SciencePolymer ChemistryPolymer EngineeringPolymer MaterialsComposite MaterialsPolymer CharacterizationPolymer CrystallinityPolymer RheologyPolymer StructurePolymer ThermodynamicsBlendingFibersHierarchical Structure FormationInterlocking SystemsRheological CharacterizationSolution BlendingUltra-high-molecular-weight PolyethyleneUltra-high-molecular-weight Polymers
Abstract In this paper, the blend fibers of ultrahigh molecular weight polyethylene (UHMWPE) and high‐density polyethylene (HDPE) were prepared by solution blending and gel spinning process. The uniformity of the blend fibers has been confirmed by rheological data and thermodynamic unimodal curve. They were further characterized by single fiber strength test, scanning electron microscopy, wide‐angle X‐ray diffraction, small‐angle X‐ray scattering, and so forth, to explore the structural evolution mechanism with the change of UHMWPE content. The results showed that when the molar content of UHMWPE was only 2.9 mol%, entanglement appeared in the structure of shish‐kebab, and when the proportion reached 20 mol%, an interlocking structure could be observed. With the increase of UHMWPE content, kebab began to be networked, and when the content reached 33 mol%, kebab's orientation reached its peak. After that, the interlocking network structure gradually improved. When the content reached 50 mol%, the shish's orientation reached saturation, and the shish‐kebab network became perfect. In addition, with the increase of UHMWPE content, stress‐induced recrystallization occurred on the wafer, some kebab would be converted into shish crystals, and when the content exceeded 50 mol%, the microfibers began to merge, and the wafer became denser, but still had entanglements. Our work has proposed a quantitative explanation for the evolution of hierarchical crystal structure of HDPE/UHMWPE blend fibers.
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Flow-induced shish-kebab precursor structures in entangled polymer melts
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