Jin, S.; Lu, R. Y.; Yan, J. Y.; Xue, Y. H. Study on gel spinning and fiber formation processing technology of ultra-high molecular weight polyethylene with different molecular weights. Acta Polymerica Sinica (in Chinese), doi: 10.11777/j.issn1000-3304.2026.26034.
Jin, S.; Lu, R. Y.; Yan, J. Y.; Xue, Y. H. Study on gel spinning and fiber formation processing technology of ultra-high molecular weight polyethylene with different molecular weights. Acta Polymerica Sinica (in Chinese), doi: 10.11777/j.issn1000-3304.2026.26034. DOI:CSTR: 32057.14.GFZXB.2026.7598.
Study on Gel Spinning and Fiber Formation Processing Technology of Ultra-high Molecular Weight Polyethylene with Different Molecular Weights
The high-performance development of ultra-high molecular weight polyethylene (UHMWPE) fibers has long been a central issue in high-strength and high-modulus polymer fibers
while the cooperative roles of raw material molecular weight
microstructure
and complex processing pathways remain insufficiently understood. In this study
spinning-grade UHMWPE resins with different molecular weights were investigated
focusing on gel spinning and multistage drawing as representative nonequilibrium processing routes. The relationships among the raw material structure
chain topological evolution
and drawing behavior were examined. It was found that increasing the molecular weight of the raw material alone did not directly improve the mechanical properties of the fiber; instead
its potential contribution was released through chain disentanglement and orientation reorganization during processing. Resins with a concentrated particle size distribution and moderate pore structures were more favorable for homogeneous swelling and the formation of stable gel network structures. By coordinating the screw temperature and rotational speed
the molecular weights of the gel fibers derived from different initial viscosity-average molecular weights were regulated and converged to approximately 3.60×10
6
g/mol. However
different temperature-shear pathways introduced path-dependent nonequilibrium chain topologies
which persisted during subsequent drawing as topological memory effects and continuously influenced the chain flexibility and fiber mechanical performance. Systems with higher chain flexibility
particularly those with intermediate molecular weights
were more suitable for achieving a high draw-ratio orientation. Overall
the results suggest that the high-performance fabrication of UHMWPE fibers depends on the cooperative regulation of chain topology an
d drawing kinetics rather than molecular weight maximization alone
providing a basis for structure-process design in UHMWPE fiber manufacturing.
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references
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