Thermal Breakage and Self-Healing of a Polymer Chain under Tensile Stress

Details Thermal Breakage and Self-Healing of a Polymer Chain under Tensile Stress Thermal Breakage and Self-Healing of a Polymer Chain under Tensile Stress

2010-02-11

arxiv.org/abs/1002.2307v1

J. Chem. Phys. 132, 204902 (2010)

Physics

Condensed Matter

Soft Condensed Matter

25 pages, 13 pictures

Scientific paper

10.1063/1.3427245

We consider the thermal breakage of a tethered polymer chain of discrete segments coupled by Morse potentials under constant tensile stress. The chain dynamics at the onset of fracture is studied analytically by Kramers-Langer multidimensional theory and by extensive Molecular Dynamics simulations in 1D- and 3D-space. Comparison with simulation data in one- and three dimensions demonstrates that the Kramers-Langer theory provides good qualitative description of the process of bond-scission as caused by a {\em collective} unstable mode. We derive distributions of the probability for scission over the successive bonds along the chain which reveal the influence of chain ends on rupture in good agreement with theory. The breakage time distribution of an individual bond is found to follow an exponential law as predicted by theory. Special attention is focused on the recombination (self-healing) of broken bonds. Theoretically derived expressions for the recombination time and distance distributions comply with MD observations and indicate that the energy barrier position crossing is not a good criterion for true rupture. It is shown that the fraction of self-healing bonds increases with rising temperature and friction.

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