期刊
JOURNAL OF THE AMERICAN CERAMIC SOCIETY
卷 105, 期 1, 页码 193-206出版社
WILEY
DOI: 10.1111/jace.18050
关键词
calcium aluminosilicates; coarsening; glass; kinetics; microstructure; nanodomains; phase separation
资金
- National Science Foundation [1762275]
- Directorate For Engineering
- Div Of Civil, Mechanical, & Manufact Inn [1762275] Funding Source: National Science Foundation
The study shows that the dynamics in glasses with nanoscale phase separation transition from LSW-type to a diffusion-controlled pseudo-coalescence mechanism at about 17% droplet volume fraction, leading to elongation and interconnection of droplets. Calcium diffusion is suggested to be the main cause for the coarsening of silica-rich domains, and the transition cannot be explained by Brownian motion or Van der Waals attraction, indicating various osmotic forces may be at play.
Glasses with nanoscale phase separation have the potential to possess improved hardness and fracture toughness while maintaining their optical transparency. Here we present the results of isothermal heat treatments of phase-separated calcium aluminosilicate glasses. Our results indicate that a transition from Lifshitz-Slozof-Wagner (LSW)-type kinetics to a diffusion-controlled pseudo-coalescence mechanism occurs at similar to 17% droplet volume fraction, which results in the droplets becoming increasingly elongated and interconnected. The activation barrier for both mechanisms suggests that calcium diffusion is the underlying means for the coarsening of the silica-rich domains. Simple approximations show the transition cannot be explained by Brownian motion or Van der Waals attraction between domains, and instead suggest various osmotic forces may be responsible.
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