RESUMEN
Green energy transition has supposed to give a huge boost to the electric vehicle rechargeable battery market. This has generated a compelling demand for raw materials, such as cobalt and nickel, which are key common constituents in lithium-ion batteries (LIBs). However, their existing mining protocols and the concentrated localization of such ores have made cobalt and nickel mineral conundrums, and their supplies experience shortages, which threaten to slow the progress of the renewable energy transition. Aiming to contribute to the sustainable recycling of these valuable metals from LIBs and wastewater, in this work, we explore the use of four mixed matrix membranes (MMMs) embedding different metal-organic frameworks (MOFs), i.e., MIL-53(Al), MIL-53(Fe), MIL-101(Fe), and {SrIICuII 6[(S,S)-serimox]3(OH)2(H2O)}·39H2O (SrCu 6 Ser) in polyether sulfone (PES), for the recovery of cobalt(II) and nickel(II) metal cations from mixed cobalt-nickel aqueous solutions containing common interfering ions. Whereas the neat PES membrane slightly contributes to the adsorption of metal ions, showing reduced removal efficiency values of 10.2 and 9.5% for Ni(II) and Co(II), respectively, the inclusion of MOFs in the polymeric matrix substantially improves the adsorption performances. The four MOF@PES MMMs efficiently remove these metals from water, with MIL-53(Al)@PES being the one that presents better performance, with a removal efficiency up to 95% of Ni(II) and Co(II). Remarkably, SrCu 6 Ser@PES exhibits outstanding selectivity toward cobalt(II) cations compared to of nickel(II) ones, with removal efficiencies of 63.7 and 15.1% for Co(II) and Ni(II), respectively. Overall, the remarkable efficiencies, versatility, high environmental robustness, and cost-effective synthesis shown by this family of MOF@PES MMMs situate them among the best adsorbents for the extraction of this kind of contaminants.
RESUMEN
Mimicking enzymatic processes carried out by natural enzymes, which are highly efficient biocatalysts with key roles in living organisms, attracts much interest but constitutes a synthetic challenge. Biological metal-organic frameworks (bioMOFs) are potential candidates to be enzyme catalysis mimics, as they offer the possibility to combine biometals and biomolecules into open-framework porous structures capable of simulating the catalytic pockets of enzymes. In this work, we first study the catalase activity of a previously reported bioMOF, derived from the amino acid L-serine, with formula {CaIICuII6[(S,S)-serimox]3(OH)2(H2O)} · 39H2O (1) (serimox = bis[(S)-serine]oxalyl diamide), which is indeed capable to mimic catalase enzymes, in charge of preventing cell oxidative damage by decomposing, efficiently, hydrogen peroxide to water and oxygen (2H2O2 â 2 H2O + O2). With these results in hand, we then prepared a new multivariate bioMOF (MTV-bioMOF) that combines two different types of bioligands derived from L-serine and L-histidine amino acids with formula CaIICuII6[(S,S)-serimox]2[(S,S)-hismox]1(OH)2(H2O)}·27H2O (2) (hismox = bis[(S)-histidine]oxalyl diamide ligand). MTV-bioMOF 2 outperforms 1 degrading hydrogen peroxide, confirming the importance of the amino acid residue from the histidine amino acid acting as a nucleophile in the catalase degradation mechanism. Despite displaying a more modest catalytic behavior than other reported MOF composites, in which the catalase enzyme is immobilized inside the MOF, this work represents the first example of a MOF in which an attempt is made to replicate the active center of the catalase enzyme with its constituent elements and is capable of moderate catalytic activity.