Liquid-vapor partitioning of HCl(aq) to 350°C

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Abstract

Partitioning of HCl(aq) between liquid and vapor phases was measured from 50–350°C at 50°C intervals by sampling the liquid and vapor phases in corrosion-resistant autoclaves. Values of the overall partitioning constant K were calculated from the observed compositions of the two phases using published activity coefficients for HCl(aq) in the liquid phase, assuming that the neutral HC1 molecule is the only solute species present in the vapor phase, and assigning a unit fugacity coefficient for vaporphase HC1. Partitioning is a strong function of temperature, with K increasing more than six orders of magnitude over the temperature range of this work. Measured values of K, including results available in the literature to 110°C, are well represented by a simple function of temperature T in Kelvin and solvent density ρ in g · cm−3: logK = −13.4944 − 934.466/T − 11.0029 logρ + 5.4847 logT.

The present measurements give directly the composition of the vapor phase over HCl(aq); partitioning of HC1 to the vapor phase over NaCl(aq) brines has been estimated through the use of approximate activity coefficients for HCl(aq) in the mixed brines.

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