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                <term xml:lang="es">alkanolamines</term>
                <term xml:lang="es">mixtures</term>
                <term xml:lang="es">solubility</term>
                <term xml:lang="es">electrolyte systems</term>
                <term xml:lang="es">n-methyldiethanolamine</term>
                <term xml:lang="es">hydrogen-sulfide</term>
                <term xml:lang="es">carbon-dioxide</term>
                <term xml:lang="es">excess gibbs energy</term>
                <term xml:lang="es">local composition model</term>
                <term xml:lang="es">vapor-liquid-equilibria</term>
                <term xml:lang="es">gas processing</term>
                <term xml:lang="es">modeling</term>
                <term xml:lang="es">hydrogen sulfide</term>
                <term xml:lang="es">carbon dioxide</term>
                <term xml:lang="es">MDEA</term>
                <term xml:lang="es">acid gas data</term>
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              <p>Aqueous amine solutions are widely used in the industry for acid gas removal. In order to treat natural gas or refinery process streams, an accurate knowledge of solubility data of carbon dioxide, hydrogen sulfide and other sulfur species in aqueous amine solutions is required. In this paper, new equilibrium measurements on 50wt% aqueous methyldiethanolamine solution with CO2 and H2S have been produced. A simple way to correlate the data has been searched and found. First, a model proposed by Posey et al. in 1996, then a Deshmukh-Mather model are used to correlate vapor-liquid equilibria. The Posey et al. model lacks accuracy to represent the experimental data, especially for high loadings. The Deshmukh-Mather model shows good agreement as long as the total loading (H2S + CO2) does not reach 1.0.</p>
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