A Novel Numerical Procedure to Estimate the Electric Charge in the Pore from Filtration of Single-Salt Solutions.

Autor: Dutournié P; Institut de Science des Matériaux de Mulhouse (IS2M-UMR CNRS 7361), Université de Haute-Alsace, 3Bis Rue Alfred Werner, CEDEX, 68098 Mulhouse, France., Daou TJ; Institut de Science des Matériaux de Mulhouse (IS2M-UMR CNRS 7361), Université de Haute-Alsace, 3Bis Rue Alfred Werner, CEDEX, 68098 Mulhouse, France., Déon S; Institut UTINAM (UMR CNRS 6213), Université de Bourgogne Franche-Comté, 16 route de Gray, CEDEX, 25030 Besançon, France.
Jazyk: angličtina
Zdroj: Membranes [Membranes (Basel)] 2021 Sep 23; Vol. 11 (10). Date of Electronic Publication: 2021 Sep 23.
DOI: 10.3390/membranes11100726
Abstrakt: The assessment of physicochemical parameters governing the transport of ions through nanoporous membranes is a major challenge due to the difficulty in experimental estimation of the dielectric constant of the solution confined in nanopores and the volumetric membrane charge. Numerical identification by adjusting their values to fit experimental data is a potential solution, but this method is complicated for single-salt solutions due to the infinite number of couples that can describe a rejection curve. In this study, a novel procedure based on physical simplifications which allows the estimation of a range of values for these two parameters is proposed. It is shown here that the evolution of the interval of membrane charge with salt concentration can be described in all the experimental conditions by the Langmuir-Freundlich hybrid adsorption isotherm. Finally, it is highlighted that considering the mean dielectric constant and the adsorption isotherms assessed from a range of concentrations allowed a good prediction of rejection curves, irrespective of the salt and membrane considered.
Databáze: MEDLINE