A choline chloride/urea natural deep eutectic solvent (ChCl NADES) was prepared via a green chemistry method and used to leach Zn and Mn oxides from conventional Zn–C scrap batteries. FTIR and ¹H NMR spectroscopy were used to characterize the NADES. The leaching kinetics of the Zn and Mn oxides was monitored at isothermal conditions (80, 100, 125, and 150 °C) and at two solid/NADES ratios: 3.3 and 10 g dm⁻³. It was possible to dissolve Zn and Mn oxides under all of tested conditions, reaching more than a 95% recovery for both metals at 150 °C after 90 min, whereas, at 25 °C, it was possible to leach up to 90% of the Zn and 30% of the Mn after 4320 min (72 h). Furthermore, the leaching kinetics was controlled by the boundary layer, coincident with a shrinking core model. According to the Arrhenius plot, the activation energy for Zn ranges from 49.13 to 52.21 kJ mol⁻¹, and that for Mn ranges from 46.97 to 66.77 kJ mol⁻¹.

This study presents a general method which can be used for the synthesis of mononuclear complexes with europium(III) and organic ligands with carboxylic groups. It describes the procedure for preparing a new mononuclear coordination complex with europium(III) and carboxylate ligands sourced from benzoic acid. The construction of mononuclear complexes with a coordination sphere saturated in carboxylic ligands must go through the preparation and purification of a europium(III) intermediate complex that presents a coordination sphere with anions that will be later exchanged for carboxylic groups and finally precipitated as a solvent-free or anion-free complex within the coordination sphere. The detailed synthesis procedure for powders of a new complex, as well as studies of its structural composition at each phase and luminescent properties, are detailed in this study. Analytical and spectroscopic data reveal the formation of a new mononuclear complex of the general formula [Eu(OOCC₆H₅)₃·(HOOCC₆H₅)₂]. The crystal structure of the Eu(III) complex was solved using X-ray powder diffraction data and EXPO2014 software, and the crystal structure result was deposited in the CCDC service with number 19771999.