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Microstructural Dynamics of Polymer Melts during Stretching: Radial Size Distribution

The transient elongational viscosity [Formula: see text] of the polymer melt is known to exhibit strain hardening, which depends on the strain rate [Formula: see text]. This phenomenon was elucidated by the difference of chain stretching in the entanglement network between extension and shear. Howev...

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Detalles Bibliográficos
Autores principales: Hsieh, Ming-Chang, Tsao, Yu-Hao, Sheng, Yu-Jane, Tsao, Heng-Kwong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10181331/
https://www.ncbi.nlm.nih.gov/pubmed/37177214
http://dx.doi.org/10.3390/polym15092067
Descripción
Sumario:The transient elongational viscosity [Formula: see text] of the polymer melt is known to exhibit strain hardening, which depends on the strain rate [Formula: see text]. This phenomenon was elucidated by the difference of chain stretching in the entanglement network between extension and shear. However, to date, the microscopic evolution of polymer melt has not been fully statistically analyzed. In this work, the radial size distributions P([Formula: see text]) of linear polymers are explored by dissipative particle dynamics during the stretching processes. In uniaxial extensional flow, it is observed that the mean radius of gyration [Formula: see text] and standard deviation [Formula: see text] remain unchanged until the onset of strain hardening, corresponding to linear viscoelasticity. Both [Formula: see text] and [Formula: see text] rise rapidly in the non-linear regime, and bimodal size distribution can emerge. Moreover, the onset of strain hardening is found to be insensitive to the Hencky strain ([Formula: see text]) and chain length (N).