Structural relaxation of porous glasses due to internal stresses and deformation under tensile loading at constant pressure
arXiv:1808.04033 · doi:10.1016/j.commatsci.2018.10.009
Abstract
The time evolution of the pore size distributions and mechanical properties of amorphous solids at constant pressure is studied using molecular dynamics simulations. The porous glasses were initially prepared at constant volume conditions via a rapid thermal quench from the liquid state to the glassy region and allowing for simultaneous phase separation and material solidification. We found that at constant pressure and low temperature, the porous network becomes more compact and the glassy systems relocate to progressively lower levels of the potential energy. Although the elastic modulus and the average glass density both increase with the waiting time, their dependence is described by the power-law function with the same exponent. Moreover, the results of numerical simulations demonstrated that under tensile loading at constant pressure, low-density porous samples become significantly deformed and break up into separate domains at high strain, while dense glasses form a nearly homogeneous solid material.
arXiv comment27 pages, 12 figures
References in corpus (8)
- Testing Mode-Coupling Theory for a Supercooled Binary Lennard-Jones Mixture I: The van Hove Correlation Function
- Influence of the glass transition on the liquid-gas spinodal decomposition
- Intermittent dynamics and logarithmic domain growth during the spinodal decomposition of a glass-forming liquid
- Slow relaxation dynamics in binary glasses during stress-controlled, tension-compression cyclic loading
- Evolution of the pore size distribution in sheared binary glasses
- Structural transformations in porous glasses under mechanical loading. I. Tension
- Structural transformations in porous glasses under mechanical loading. II. Compression
- Distributions of pore sizes and atomic densities in binary glasses revealed by molecular dynamics simulations