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dc.contributor.authorCoterillo Ruisánchez, Raúl 
dc.contributor.authorGallart Tauler, Lien Ester
dc.contributor.authorFernández-Escalante Barquín, Elena 
dc.contributor.authorJunquera Quintana, Francisco Javier 
dc.contributor.authorGarcía Fernández, Pablo (físico) 
dc.contributor.authorOrtiz Uribe, Inmaculada 
dc.contributor.authorIbáñez Mendizábal, Raquel 
dc.contributor.authorSan Román San Emeterio, María Fresnedo 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-03-22T12:19:49Z
dc.date.available2023-03-22T12:19:49Z
dc.date.issued2022-06-15
dc.identifier.issn0011-9164
dc.identifier.otherPID2020-115409RB-I00es_ES
dc.identifier.urihttps://hdl.handle.net/10902/28314
dc.description.abstractLithium, declared critical raw material by the European Union in 2020, is a competitor to hydrogen as alternative to petroleum. Its use is increasing while reserves are declining, boosting new sources, as seawater desalination concentrates. In this work, a computational study of the most promising extractants, B-diketones and organophosphates and combinations thereof, towards lithium in presence of metal ions found in the concentrates, Na+, K+, Mg2+, Ca2+ and Sr2+ was carried out, via molecular simulation using ab initio Density Functional Theory (DFT). The geometries, reaction energies, and thermodynamic parameters have been evaluated. Using the square of the electronic wave function an electrostatic interaction was confirmed as cation-extractant/s bonding. The complexation reaction energies of the systems formed by a cation and a single extractant display negative [delta]E and [delta]G values, pointing towards stable complexes and spontaneous reactions. The synergic effect of extractants was studied by combining the [beta]-diketones with TOPO (1:1) leading to an increase of [delta]E and [delta]G (absolute value). The extraction coefficient, K, follows the order K(K+) > K(Na+) > K(Li+) > K(Sr2+) > K(Ca2+) > K(Mg2+). In consequence, selectivity Li+ towards cations of the group II was higher, S(Li+/Mg2+) > S(Li+/Ca2+) > S(Li+/Sr2+) for the combined mixtures BTA TOPO and FDOD TOPO and lower towards group I cations, S(Li+/Na+) > S(Li+/K+) for DBM TOPO and LIX54 TOPO. The selectivity of Li+ regarding the rest of the cations and the 16 extractants and mixtures of extractants was lower than the selectivity of Li+ with respect to each cation, being the best value for the DBM TOPO and LIX54 TOPO systems. The results obtained are expected to provide a tool on the behaviour of the most promising of extractants towards Li+ in seawater desalination concentrates.es_ES
dc.description.sponsorshipThis research was developed in the framework of the project PID2020-115409RB-I00 financed by the Ministry of Science and Innovation (Spain).es_ES
dc.format.extent13 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationales_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceDesalination, 2022, 532, 115704es_ES
dc.subject.otherLithiumes_ES
dc.subject.otherExtractiones_ES
dc.subject.otherSeawater desalination concentrateses_ES
dc.subject.otherDensity Functional Theory (DFT)es_ES
dc.subject.otherEquilibrium and selectivityes_ES
dc.titleSelective extraction of lithium from seawater desalination concentrates: study of thermodynamic and equilibrium properties using Density Functional Theory (DFT)es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.desal.2022.115704es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.desal.2022.115704
dc.type.versionpublishedVersiones_ES


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Attribution-NonCommercial-NoDerivatives 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution-NonCommercial-NoDerivatives 4.0 International