During fracture amorphous oxides exhibit irreversible processes, including inelastic and nonrecoverable relaxation effects in the process zone surrounding the crack tip. Here, classical molecular dynamics simulations were used with a reactive forcefield to evaluate inelastic relaxation processes in five amorphous sodium silicate compositions. Overall, the 20% Na2O-SiO2(NS20) composition exhibited the most inelastic relaxation, followed by the 15% Na2O-SiO2(NS15) composition, the 25% Na2O-SiO2(NS25) composition, and finally the 10% (NS10) and 30% (NS30) Na2O-SiO2 compositions. Coordination analysis of the Na+ ions identified that during inelastic relaxation the Na+ ions were increasingly coordinated by nonbridging oxygens (NBOs) for the NS10 and NS15 compositions, which was supported by radial analysis of the O-Na-O bond angles surrounding the crack tip. Across the sodium silicate compositional range, two different inelastic relaxation mechanism were identified based on the amount of bridging oxygens (BOs) and NBOs in the Na+ ion coordination shell. At lower (NS10) and higher (NS30) sodium compositions, the entire structured relaxed toward the crack tip. In contrast at intermediate sodium concentrations (NS20) the Na+ ion migrates toward the crack tip separately from the network structure. By developing a fundamental understanding of how modified silica systems respond to static stress fields, we will be able to predict how varying amorphous silicate systems exhibit slow crack growth.
Rimsza, Jessica M. and Jones, Reese E.. "Inelastic relaxation processes in amorphous sodium silicates." Journal of the American Ceramic Society, vol. 107, no. 3, Aug. 2023. https://doi.org/10.1111/jace.19435
Rimsza, Jessica M., & Jones, Reese E. (2023). Inelastic relaxation processes in amorphous sodium silicates. Journal of the American Ceramic Society, 107(3). https://doi.org/10.1111/jace.19435
Rimsza, Jessica M., and Jones, Reese E., "Inelastic relaxation processes in amorphous sodium silicates," Journal of the American Ceramic Society 107, no. 3 (2023), https://doi.org/10.1111/jace.19435
@article{osti_2311446,
author = {Rimsza, Jessica M. and Jones, Reese E.},
title = {Inelastic relaxation processes in amorphous sodium silicates},
annote = {During fracture amorphous oxides exhibit irreversible processes, including inelastic and nonrecoverable relaxation effects in the process zone surrounding the crack tip. Here, classical molecular dynamics simulations were used with a reactive forcefield to evaluate inelastic relaxation processes in five amorphous sodium silicate compositions. Overall, the 20% Na2O-SiO2(NS20) composition exhibited the most inelastic relaxation, followed by the 15% Na2O-SiO2(NS15) composition, the 25% Na2O-SiO2(NS25) composition, and finally the 10% (NS10) and 30% (NS30) Na2O-SiO2 compositions. Coordination analysis of the Na+ ions identified that during inelastic relaxation the Na+ ions were increasingly coordinated by nonbridging oxygens (NBOs) for the NS10 and NS15 compositions, which was supported by radial analysis of the O-Na-O bond angles surrounding the crack tip. Across the sodium silicate compositional range, two different inelastic relaxation mechanism were identified based on the amount of bridging oxygens (BOs) and NBOs in the Na+ ion coordination shell. At lower (NS10) and higher (NS30) sodium compositions, the entire structured relaxed toward the crack tip. In contrast at intermediate sodium concentrations (NS20) the Na+ ion migrates toward the crack tip separately from the network structure. By developing a fundamental understanding of how modified silica systems respond to static stress fields, we will be able to predict how varying amorphous silicate systems exhibit slow crack growth.},
doi = {10.1111/jace.19435},
url = {https://www.osti.gov/biblio/2311446},
journal = {Journal of the American Ceramic Society},
issn = {ISSN 0002-7820},
number = {3},
volume = {107},
place = {United States},
publisher = {American Ceramic Society},
year = {2023},
month = {08}}
Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences, Vol. 221, Issue 582-593https://doi.org/10.1098/rsta.1921.0006