Molecular-dynamics simulations of water-benzene mixtures at 573 K and pressures in the 85–140 bars range have been performed to examine local structure and dynamics of the mixtures, which exhibit anomalously large volume expansion on mixing as recently found by in situ near-infrared measurements. Fractional charges for a simple-point-charge-type potential of water were adjusted so as to reproduce liquid densities and the gas-to-liquid transition pressure of neat water at 573 K. A Lennard-Jones-type potential for benzene was used and the Lorentz-Berthelot combination rule was applied to the water-benzene interaction. Simulations with a N-P-T ensemble of 800-molecule system have been performed and the results reproduce well the anomalous volumetric behavior of the mixtures with the mole fraction of benzene in the 0.3–0.8 range. Pair distribution functions, coordination numbers, and self-diffusion coefficients for the mixtures are calculated, and it is suggested that the local structure around water molecules undergoes drastic change by dissolution of benzene in the vicinity of the critical region, but that around benzene molecules seems to be understood as that of ordinary liquid mixtures.
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