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Biomedical subjects

K S Pitzer

Publications and source records attributed to K S Pitzer.

6 recordsLinked to original sources

Critical phenomena and thermodynamics of dilute aqueous sodium chloride to 823 K.

Semiempirical equations are developed that represent the behavior of dilute solutions of NaCl in water (steam) in the range 723-823 K where ion pairing is extensive. This supplements the equations given earlier for more concentrated solutions. In this temperature range the system NaCl/H(2)O shows critical behavior with two phases below the critical pressure. The equations for the dilute solutions yield critical behavior. Though the equations for concentrated solutions do not yield critical behavior at the critical pressure, only a very small interpolation function is required to connect smoothly the two equations. The ion-pairing equilibrium constants are reported as well as the Gibbs energies of hydration for both ions and ion pairs.

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Dielectric constant of water at very high temperature and pressure.

Pertinent statistical mechanical theory is combined with the available measurements of the dielectric constant of water at high temperature and pressure to predict that property at still higher temperature. The dielectric constant is needed in connection with studies of electrolytes such as NaCl/H(2)O at very high temperature.

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Thermodynamics of aqueous sodium chloride to 823 K and 1 kilobar (100 MPa).

It is shown that a very simple semiempirical equation represents quite accurately the thermodynamic properties of aqueous sodium chloride from 373 to 823 K. The equation comprises one Margules term and a Debye-Hückel term. Just the one Margules parameter is freely adjustable because the Debye-Hückel parameter is determined by the properties of water. The equation is valid from the saturation composition down to infinite dilution for solvent density above 0.75 g.cm(-3) but at lower density only above a solute mole fraction of about 0.1 on an ionized basis. Both solute and solvent activity coefficients are fitted from the lowest pressure of solution existence up to 1 kilobar (1 bar = 100 kPA). Derivation of enthalpy and other related functions is discussed.

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Phase equilibria for highly unsymmetrical plasmas and electrolytes.

The conclusion of classical Debye-Hückel theory that a phase separation may occur in highly unsymmetrical plasmas or electrolytes is shown to be false and to arise from a serious error in the treatment of the interaction of pairs of the most highly charged ions. After an approximate correction for this error, no phase separation is predicted. Specific application to iron in the solar plasmas is discussed.

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