Abstract
The diffusion of water in silica glass was measured as a function of applied uniaxial stress and hydrostatic pressure at selected temperatures. It was found that the diffusion coefficient of water increased exponentially with increasing tensile stress and decreased with increasing compressive stress and increasing hydrostatic pressure. The activation volume for water diffusion in silica glass was found to be ∼170 cm3/mol at 192°C and ∼72 cm3/mol at 350°C. The solubility of water in glass showed a trend opposite to the diffusion coefficient, namely, it decreased exponentially with increasing tensile stress and increased with increasing compressive stress and hydrostatic pressure. These stress (or pressure) dependences were attributed to the shift of the glass‐water reaction equilibrium.
Published Version
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