ABSTRACT
Thermodynamic properties of fluids confined in nanopores differ from those observed in the bulk. To investigate the effect of nanoconfinement on water compressibility, we perform water sorption experiments on two nanoporous glass samples while concomitantly measuring the speed of longitudinal and shear ultrasonic waves in these samples. These measurements yield the longitudinal and shear moduli of the water-laden nanoporous glass as a function of relative humidity that we utilize in the Gassmann theory to infer the bulk modulus of the confined water. This analysis shows that the bulk modulus (inverse of compressibility) of confined water is noticeably higher than that of the bulk water at the same temperature. Moreover, the modulus exhibits a linear dependence on the Laplace pressure. The results for water, which is a polar fluid, agree with previous experimental and numerical data reported for nonpolar fluids. This similarity suggests that irrespective of intermolecular forces, confined fluids are stiffer than bulk fluids. Accounting for fluid stiffening in nanopores may be important for accurate interpretation of wave propagation measurements in fluid-filled nanoporous media, including in petrophysics, catalysis, and other applications, such as in porous materials characterization.
ABSTRACT
The primary goal of this study was to characterize the influence of the pore-saturated gas media and their physical properties on the elasticity of porous ceramic materials. Resonant ultrasound spectroscopic measurements were performed on test specimens of alumina with ~40% porosity, zirconia with ~48% porosity, and sintered fully dense zirconia to determine the hydrostatic pressure-dependent macroscopic elasticity. Here, we report the variation of elasticity of porous and full dense samples over approximately five orders of magnitude (800-0.02 psi) in absolute pressure. The time evolution of mechanical equilibrium of the porous materials at low pressure and high-temperature conditions will also be discussed.
