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Developing greener hydrometallurgical processes implies offering alternatives to conventional solvents used for liquid‐liquid extraction (LLE) of metals. In this context, it is proposed to substitute the organic phase by a hydrophobic silica‐based porous liquid (PL). Two different sulfonated hollow silica particles (HSPs) are modified with various polyethoxylated fatty amines (EthAs) forming a canopy that provides both the targeted hydrophobicity and liquefying properties. This study shows that these properties can be tuned by varying the number of ethylene oxide units in the EthA: middle‐range molecular weight EthAs allow obtaining a liquid at room temperature, while too short or too long EthA leads to solid particles. Viscosity is also impacted by the density and size of the silica spheres: less viscous PLs are obtained with small low‐density spheres, while for larger spheres (c.a. 200 nm) the density has a less significant impact on viscosity. According to this approach, hydrophobic PLs are successfully synthesized. When contacted with an aqueous phase, the most hydrophobic PLs obtained allow a subsequent phase separation. Preliminary extraction tests on three rare earth elements have further shown that functionalization of the PL is necessary to observe metal extraction. [ABSTRACT FROM AUTHOR]

The removal of heavy toxic metals from industrial effluents is extremely important, especially for mercury (Hg), which is classified as a highly toxic even at low concentrations. For this purpose, novel thiourea chelating resins were synthesized as sorbent for Hg (II). Six different polymers of formo‐phenolic types were characterized and evaluated for their chelating properties with respect to Hg (II) extraction. Batch adsorption studies of mercury (II) as a function of pH, initial metal ion concentration, temperature, and time showed that thiourea formo‐phenolic polymers have a good affinity for Hg removal and a high adsorption capacity. Adsorption isotherms (Langmuir and Freundlich) and kinetic models (pseudo‐first and pseudo‐second order) were used to interpret the sorption behavior of the materials. The Langmuir model yielded the best fit with a maximum adsorption capacity of 300 mg/g. Desorption studies were performed with aqueous thiourea solution and showed that the adsorbent is indeed regenerable and can be effectively used for up to three adsorption‐desorption cycles with negligible loss of performance. This study confirmed the potential of thiol‐modified formo‐phenolic resins in sorbent engineering with promising applications in the remediation of mercury‐contaminated water. [ABSTRACT FROM AUTHOR]

In this present study, we developed a new series of sorbents based on phenolic foam resin for the extraction of rare earth elements. Chelating phenolic foams were prepared using appropriate formulation of blowing agent, surfactant and curing acid agent and a prepolymer resulting from an alkaline polymerisation reaction of phenolic diglycolamide derivative with admixture of phenol, catechol or resorcinol in the presence of formaldehyde as crosslinker agent. The foaming copolymer resins were completely described and engaged in sorption studies with three types of lanthanide (La, Eu, Yb), which represent light, medium and heavy REEs, respectively. [ABSTRACT FROM AUTHOR]

This study investigates uranium solvent extraction under AMEX process conditions. The use of pure extractants without diluents or phase modifiers allows us not only to reduce the use of volatile organic compounds but also to provide higher extraction yields without third-phase formation. Pure extractants are protonated amines or quaternary ammoniums with suitable counter ions, which act at the interface between ion pairs and protic ionic liquids. The mixture of sulphates anion (SO42−) and bis(trifluoromethanesulfonyl)imide anion (NTf2−) revealed unexpected nonlinear extraction behaviors, which appear highly important to rationalize for optimized application. A spectroscopic analysis (NMR, UV-vis, FT-IR, and EXAFS) showed that uranium extraction occurs via a protonated amine and three sulphates. A nonlinear extraction could further be interpreted by considering a water and acid transfer between the two phases: at lower sulphate ratios, the release of acid from the organic phase into the aqueous phase was shown to influence the number of protonated amines in the organic phase, affecting uranium extraction before its enhancement. Furthermore, the extraction loss at higher sulphate ratios was assigned to the destabilization of bidentate uranium–sulphate complexes due to a competition between water and sulphates. [ABSTRACT FROM AUTHOR]

This work reports the synthesis of formo‐phenolic resins containing four catecholamide (CAM) moieties with admixture of phenol, catechol or resorcinol. These chelating resins have been developed to selectively extract U(VI) from seawater. This media is a challenging environment due to a pH around 8.2 and a large excess of alkaline and earth‐alkaline cations. From the various sorption experiments investigated, the results indicate that the synthesized material exhibit good sorbent properties for U(VI) with uptake capacity about 50 mg/g for the more promising resins with a pronounced selectivity for uranium even under saline conditions. Thermodynamic and kinetic adsorption data were determined for the best resin (Langmuir adsorption model and pseudo‐second order model). [ABSTRACT FROM AUTHOR]

Efficient and selective extractions of precious and critical metal ions such as Au(III) and Pd(II) were investigated using zirconia nanoparticles surface modified with different organic mono- and di-carbamoyl phosphonic acid ligands. The modification is made on the surface of commercial ZrO2 that is dispersed in aqueous suspension and was achieved by optimizing the Bronsted acid–base reaction in ethanol/H2O solution (1:2), resulting in inorganic–organic systems of ZrO2-Ln (Ln: organic carbamoyl phosphonic acid ligand). The presence, binding, amount, and stability of the organic ligand on the surface of zirconia nanoparticles were confirmed by different characterizations such as TGA, BET, ATR-FTIR, and 31P-NMR. Characterizations showed that all the prepared modified zirconia had a similar specific surface area (50 m2.g−1) and the same amount of ligand on the zirconia surface in a 1:50 molar ratio. ATR-FTIR and 31P-NMR data were used to elucidate the most favorable binding mode. Batch adsorption results showed that (i) ZrO2 surface modified with di-carbamoyl phosphonic acid ligands had the highest adsorption efficiency to extract metals than mono-carbamoyl ligands, and (ii) higher hydrophobicity of the ligand led to better adsorption efficiency. The surface-modified ZrO2 with di-N,N-butyl carbamoyl pentyl phosphonic acid ligand (ZrO2-L6) showed promising stability, efficiency, and reusability in industrial applications for selective gold recovery. In terms of thermodynamic and kinetic adsorption data, ZrO2-L6 fits the Langmuir adsorption model and pseudo-second-order kinetic model for the adsorption of Au(III) with maximum experimental adsorption capacity qmax = 6.4 mg.g−1. [ABSTRACT FROM AUTHOR]