Nowadays, solving the problem of rational, integrated use of the mined raw materials, the transition to waste-free technologies for its processing is a crucial task. The sulfuric acid technology used for the processing of apatite concentrates on a large industrial scale does not provide the associated extraction of accompanying valuable components—rare earth metals (REM). During apatite concentrate processing, rare-earth metals are affected by the technology-related dispersion, being distributed between the insoluble leaching residue and phosphoric acid solution sent to the production of fertilizers. The necessity of a cost-effective method development for the extraction of rare earth metals is quite obvious already in connection with the indicated significance of the problem. Phosphoric acid solutions that simulate the composition of industrial phosphoric acid solutions of the following composition 4.5 mol/L H₃PO₄, 0.19 mol/L H₂SO₄ and 0.10–0.12% REM were selected as the object of research. The extraction of rare earth metals was carried out using polymers containing a fixed layer of an extractant—di-2-ethylhexylphosphoric acid (D2EHPA). Fixed layer was obtained by impregnation-saturation (solvent-impregnated resin (SIR)) or by the introduction of an extractant at the stage of polymer matrix synthesis (extractant-resin extraction (ERE)). The work determined the thermodynamic and technological characteristics of the solid-phase extraction of rare earth elements from phosphoric acid solutions with polymers impregnated with D2EHPA and containing a rigidly fixed extractant in a styrene-divinylbenzene resin matrix. The possibility of effective multiple use of polymeric resins containing D2EHPA, regenerated with a solution of 1 mol/L sodium citrate, was revealed.

The kinetic features of solvent and solid-phase extraction of yttrium and iron (III) from simulated and industrial phosphoric acid solutions are revealed. Di-2-ethylhexylphosphoric acid (D2EHPA) was used as a liquid extractant, and D2EHPA-containing Levextrel resin—a co-polymerization product of styrene and divinylbenzene in the presence of D2EHPA—was used as a solid-phase extraction agent. Significant dependence of yttrium extraction rate constant on the stirring rate was revealed using the formal first-order kinetic equation. The data obtained characterizes a diffusion-limited process with an activation energy of 16.2 ± 1.3 kJ/mol. Temperature increase during the iron (III) extraction process leads to a changeover of a rate-limiting stage from kinetic to diffusion, accompanied by drop of activation energy from 40.0 ± 1.4 to 11.4 ± 1.2 kJ/mol. Effective separation of elements at the extraction stage is possible at temperatures of 283–300 K under non-equilibrium conditions of the ferric ions transport from aqueous to organic phase. This condition ensures a high yttrium–iron separation coefficient of 23.2 in 1.5–2 min. Extraction kinetics by Levextrel resin are described by Fick’s second law equation, which establishes the laws of diffusion in the solid grain of the organic phase with an activation energy of 18.5 ± 2.0 kJ/mol.

The effective purification of large-capacity wastewater from heavy non-ferrous metals and organic pollutants using inexpensive sorption technology remains a crucial task. Analyzing the current objectives of sustainable development, biochar obtained from chicken manure has prospects as a source for sorption purification of industrial wastewater. To determine the characteristics of organic material and the composition of the initial and equilibrium phases, the following analysis methods were used: volumetric, complexometric, pH-metric, X-ray fluorescence, chromatographic, spectrophotometric, luminescence-photometric and X-ray diffraction. The thermal nitrogen desorption method was used for determining the specific surface area and pore sizes with the Quantachrome Nova 1000e automatic analyzer. The sorption properties of the reprocessing product of the fresh poultry manure were investigated in relation to organic and inorganic compounds: phenols, benzene, ketones, cations of lead, mercury, manganese and iron. Based on the results obtained, technical conditions were developed for the use of the reprocessed organic waste-based product as a sorption material for household, industrial and technological wastewater purification from organic and inorganic components.

The separation and concentration processes of heavy rare-earth metals—yttrium, ytterbium, erbium, and dysprosium—during stripping from the organic phase based on di-2-ethylhexylphosphoric acid (D2EHPA, or DEHPA) solutions were investigated in this work. Optimal conditions providing high separation factors of rare-earth metals (REM) and their extraction degree to the aqueous phase were determined. The usage of sulfuric acid solutions with a concentration of 2–6 mol/L, depending on the type of extracted rare-earth element, was proposed as a stripping agent for rare-earth metals (REM), and the usage of oxalic acid solution was proposed as an iron stripping solution from the organic phase. To increase the REM stripping efficiency, the antagonistic effect of tributyl phosphate in the di-2-ethylhexylphosphoric acid-kerosene-tributyl phosphate system was considered. The possibility of increasing the capacity of the organic solvent by cleaning the organic phase from iron ions using oxalic acid solutions was revealed. The influence of temperature, aqueous and organic phase ratio, stirring rate, and re-extractant concentration on the distribution and separation factors of adjacent heavy rare-earth-metal (HREM) pairs during the re-extraction process were determined. A schematic diagram of the laboratory-tested separation process of heavy rare-earth metals into individual components with the obtaining of yttrium and ytterbium concentrates containing more than 99% of the target components was proposed.

The mechanism of rare earth metal (REM) extraction with the organic solvent called di-2-ethylhexyl phosphoric acid (DEHPA) has been studied in this paper. Using the physicochemical method for the investigation of the composition of organic REM complexes with the extractant, the solvation numbers of the lanthanides were determined. The growth of solvation numbers from neodymium (2) to ytterbium (5) is explained by an increase in the effective charge of the REM atom and, as a result, an increase in the relative stability of the chelating REM complexes with the extractant. The composition of the organic complexes of REM with DEHPA was confirmed by infrared and Raman spectroscopy. The values of the effective thermodynamic constants and standard Gibbs energies of the extraction process are calculated. The increase in the relative stability of lanthanide complexes with DEHPA correlates with a decrease in the ionic radius of the REM.

A mechanism of extraction of cerium by tributyl phosphate (TBP) from phosphate solutions using model and production solutions containing, %: 26–28 P2O5, 1.2–2.8 SO3, 0.3–0.8 CaO, 0.1–0.4 Al2O3,...