Abstract

The distribution of volume relaxation times in a critical oxide mixture is calculated from longitudinal and shear modulus measurements. Ultrasonic relaxation allows the investigation of two distinct effects in the distribution of relaxation times as the temperature is lowered toward the critical point. At high temperatures, a coupling between the compressional component of the ultrasonic wave and supercritical fluctuations in composition leads to an anomalous broadening of the distribution of volume relaxation times. This interaction allows a measure of the average composition fluctuation lifetime, τ D, as a function of temperature. At lower temperatures, as τ D becomes longer than the volume relaxation times, the behavior of the distribution follows closely the predictions of an environmental relaxation model proposed by these authors for the analysis of shear relaxation processes in the same material.

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