Abstract
Vapor—liquid equilibrium data for aqueous solutions of volatile weak electrolytes are needed in designing separation equipment in the chemical and oil-related industries. Because of chemical reactions between the weak base ammonia and sour gases like carbon dioxide and hydrogen sulfide, modeling of phase equilibria in such mixtures requires a lot of experimental information which is rarely found in the literature. Thus, it is not surprising that published correlations are often considered unreliable. More and better experimental material is essential to overcome this situation. Therefore vapor—liquid equilibrium in the ternary system ammonia—carbon dioxide—water was investigated experimentally in the temperature range between 333.15 and 393.15 K at pressures up to about 7 MPa. The investigated concentration range covers water-rich mixtures to about 16 molal for ammonia and 13 molal for carbon dioxide. Altogether 559 data points are reported. In the region where both investigations overlap, the new experimental results are in good agreement with data reported by Müller et al. (1988). For comparison with existing correlations the method by Edwards et al. (1978) with recently published parameters (Kawazuishi and Prausnitz, 1987) is used. Predicted data agree well with the experimental results at low solute concentrations, but large deviations are observed near the minimum of the total pressure curve (in a plot vs. the concentration of carbon dioxide at constant concentrations of ammonia) and at very high solute molalities.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.