Measurement and modelling of liquid density (298.15 and 313.15 K) and vapour pressure osmometry (313.15 K) for binary aqueous solutions of organic salts

• Tipo: Artigo em Revista Científica Internacional
• Data: 2024

Autores

Velho, P (Autor) Outra; Sousa, E (Autor) Outra; Macedo, A (Autor) Outra

Revista

Título: Journal of Chemical Thermodynamics

Vol. 194

ISSN: 0021-9614

Editora: Elsevier

Indexação

Scopus - 0 Citações

Outras Informações

ID Authenticus: P-010-4P7

DOI: 10.1016/j.jct.2024.107287

Abstract (EN): Due to the eco-friendliness of organic salts, they have been gradually replacing other electrolytes in different fields of chemistry. For example, they provide biocompatible salting-out agents for liquid¿liquid extractions and earth-abundant materials for flow batteries. Nevertheless, reliable liquid density and vapour pressure data, which are paramount for a proper parameterisation of thermodynamic models, are often hard to find for aqueous solutions of organic salts, delaying the development of these technologies. In this work, the liquid density (¿) of five binary aqueous solutions of organic salts (disodium tartrate, sodium potassium tartrate, dipotassium tartrate, trisodium citrate and tripotassium citrate) were measured and correlated at 298.15 and 313.15 K and 0.1 MPa. In these assays, second-degree polynomials provided determination coefficients (R2) larger than 0.9982 in the correlation of liquid density with salt molality, for which a very accurate description of this property was accomplished. Moreover, vapour pressure osmometry (VPO) studies were carried out for these solutions at 313.15 K and 0.1 MPa. Then, the obtained osmotic coefficients (¿) were successfully modelled using the Extended Pitzer Model of Archer, yielding standard deviations (¿¿) lower than 8.61·10-3. Finally, the mean molal activity coefficients (¿±) and excess Gibbs free energies (GE/RT) of the binary aqueous solutions of organic salts were effectively calculated, with potassium- and tartrate-based salts attaining significantly higher values than the ones composed of sodium and citrate, hinting at a more ideal solution behaviour of the former. © 2024 The Author(s)

Idioma: Inglês

Tipo (Avaliação Docente): Científica