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Molecular Dynamics Simulation of Electrolyte Solutions in Ambient and Supercritical Water. 2. Relative Acidity of HCl

1996; American Chemical Society; Volume: 100; Issue: 7 Linguagem: Inglês

10.1021/jp952195g

1541-5740

Perla B. Balbuena, Keith P. Johnston, Peter J. Rossky,

Subcritical and Supercritical Water Processes

Molecular dynamics−free energy perturbation simulations are used to study the acidity of HCl relative to water at conditions ranging from ambient density and temperature to several supercritical water states. An increase in temperature from 25 °C to the critical temperature Tc (374 °C) along the coexistence curve reduces the difference between the pKa of HCl and pKw by a factor of 2. However, the corresponding difference in free energies of dissociation remains constant, even in supercritical water, along isochoric and isothermal (between 0.29 and 0.087 g/cm3) paths. This new observation is explained in terms of the effect of temperature on the thermodynamic properties of solvation of the various reacting species and is used to gain further insight into the behavior of previous experimental data.