Multiple Cracks Propagate Simultaneously in Polymer Liquids in Tension
Author(s) -
Qian Huang,
Nicolas J. Alvarez,
Aamir Shabbir,
Ole Hassager
Publication year - 2016
Publication title -
physical review letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.688
H-Index - 673
eISSN - 1079-7114
pISSN - 0031-9007
DOI - 10.1103/physrevlett.117.087801
Subject(s) - materials science , viscoelasticity , fracture mechanics , composite material , brittleness , tension (geology) , fracture (geology) , dissipation , strain energy release rate , mechanism (biology) , polymer , crack closure , crack growth resistance curve , fracture toughness , stress (linguistics) , mechanics , ultimate tensile strength , thermodynamics , physics , linguistics , philosophy , quantum mechanics
Understanding the mechanism of fracture is essential for material and process design. While the initiation of fracture in brittle solids is generally associated with the preexistence of material imperfections, the mechanism for initiation of fracture in viscoelastic fluids, e.g., polymer melts and solutions, remains an open question. We use high speed imaging to visualize crack propagation in entangled polymer liquid filaments under tension. The images reveal the simultaneous propagation of multiple cracks. The critical stress and strain for the onset of crack propagation are found to be highly reproducible functions of the stretch rate, while the position of initiation is completely random. The reproducibility of conditions for fracture points to a mechanism for crack initiation that depends on the dynamic state of the material alone, while the crack profiles reveal the mechanism of energy dissipation during crack propagation.
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