Platinum group metals (PGMs), including palladium, play a pivotal role in various industries due to their unique properties. Palladium is frequently employed in technologies aimed at environmental preservation, such as catalytic converters that reduce harmful emissions from vehicles, and in the production of clean energy, notably in the hydrogen evolution process. Regrettably, the production of this vital metal for our environment is predominantly centered in two countries—Russia and South Africa. This centralization has led to palladium being classified as a critical raw material, emphasizing the importance of establishing a secure and sustainable supply chain, as well as employing the most efficient methods for processing materials containing palladium. This review explores techniques for palladium production from primary sources and innovative recycling methods, providing insights into current technologies and emerging approaches. Furthermore, it investigates the economic aspects of palladium production, including price fluctuations influenced by emission regulations and electric vehicle sales, and establishes connections between palladium prices, imports from major producers, as well as copper and nickel prices, considering their often co-occurrence in ores.

This paper describes a single-stage synthesis process for activated carbon using cherry seeds. The influences of the carbonization temperature and the time were investigated. Using the BET method, the surface area of the obtained activated carbons was determined, as well as the pore distribution, while SEM images provided further insight into the structure of the surface. Next, the adsorption isotherm was derived. For the test, Pd(II) chloride complex ions were used. It was found that the obtained activated carbon were suitable for palladium(II) recovery from diluted aqueous solutions. Out of the tested parameters of carbon synthesis, the most optimal one was found to be 500 °C for 3 h. Additionally, it was confirmed that the increase in the adsorption temperature affects the increase in palladium load from 1.6 mg/g at 20 °C to 15.6 mg/g at 50 °C (for the best-performing sample). This fact may suggest that the process of adsorption is associated with chemical reactions.

This study investigates the synthesis, characterization, and potential applications of silver–copper (AgCu) alloy powders produced from co-precipitated carbonates. The Cu/Ag carbonate samples were analyzed using EDXRF, TGA-DSC, XRD, SEM, and electrical conductivity tests to examine their composition, thermal behavior, structure, and morphology. The results showed slight deviations from the theoretical Cu/Ag ratios in the carbonates, attributed to equilibrium effects during precipitation. Thermal analysis indicated that the reduction process of carbonates with hydrogen was completed at 300 °C, while alloy formation was confirmed by endothermic peaks around 780 °C. XRD and SEM analyses revealed that AgCu alloys formed a solid solution, with smaller crystallite sizes observed at higher Cu contents. Electrical conductivity tests demonstrated that while pure Ag and Cu powders exhibited conductivity increases with compaction, the AgCu alloy showed stable conductivity without a significant decrease. In Pd(II) cementation experiments, AgCu alloys demonstrated higher efficiency in Pd(II) recovery than pure Ag and Cu. These findings suggest that AgCu alloys, particularly with a balanced composition, may offer improved performance for metal recovery applications, providing a promising approach for industrial cementation processes.

This study explores the impact of nitrate ions on the efficiency of cementing noble metals from diluted waste solutions at a temperature of 30 °C. The research involved measuring the effectiveness of different cementing metals (such as Zn, Al, Mg, and Fe) in the presence of nitrate ions by assessing the change in metal ion concentrations before and after the cementation process using spectrometric analysis. Initial concentrations of noble metals ware Pt = 5 ppm, Au = 7.5 ppm, Pd = 5 ppm, and Rh = 1 ppm. Kinetic studies revealed that 24 h is adequate to achieve apparent equilibrium in solutions with pH 2 and 1 M nitrate ion content. The study identified significant recovery losses for gold and platinum in nitrate solutions, underlining the necessity of nitrate-free solutions in recycling. Zinc and magnesium were effective in cementing Pd and Rh, while aluminum was efficient for Pt reduction in each condition. Complete removal of Au was not achieved with any tested metal, indicating a need for alternative methods.

Oxidative leaching, as a basic step of the hydrometallurgical process of pure copper production from chalcopyrite, is a slow process in which mineral acids with strong oxidants addition are usually used as a leaching medium. It was found experimentally that the copper leaching from chalcopyrite in the H₂SO₄–H₂O₂–H₂O system, in the presence of isopropanol (IPA) and under other conditions (H₂O₂ concentration, rate of mixing and temperature), takes place with satisfactory rate and efficiency. To quantify how much the change of these crucial variables affects the rate of the process, experimentally obtained kinetic curves (conversion over time) were analyzed using a Shrinking Core Model (SCM). The determined values of the copper leaching rate constants (k_obs) confirmed the positive influence of increasing IPA and H₂O₂ concentrations as well as the temperature on the kinetics and efficiency of the leaching. The kinetic studies were also supported by using X-ray diffraction (XRD), ⁵⁷Fe Mössbauer spectroscopy, scanning electron microscopy (SEM), and adsorption measurements. The positive influence of IPA was explained by its stabilizing role for iron compounds (hematite, magnetite, and pyrite), which are catalysts during the Cu dissolution, as well as H₂O₂ protection from decomposition during free radical reactions. Finally, the optimal conditions for efficient leaching, the rate-limiting step as well as the mechanism suggestion of the copper dissolution, were given.

The rising demand for platinum-group metals, driven by their essential applications in catalysis, energy storage, and chemical conversion, underscores the need to identify new sources for their recovery. Waste solutions originating from industrial processes offer a promising alternative source of noble metals. However, due to their typically low concentrations, effective recovery requires a highly targeted approach. In this study, we present a synthetic waste solution containing trace amount of Rh(III) ions as both a medium for metal ion recovery and a direct precursor for catalyst synthesis. Using a bimodal water–ethanol solvent system, ultra-small rhodium nanoparticles were synthesized and subsequently immobilized onto activated carbon fibers (ACFs) within a microreactor system. The resulting Rh@ACF catalyst demonstrated high efficiency in the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP), serving as a model catalytic reaction. The Rh@ACF catalyst, containing 4.24 µg Rh per milligram of sample, exhibited notable catalytic activity, achieving 75% conversion of 4-NP to 4-AP within 1 h. Full conversion to 4-AP was also reached within 5 min, but requires extra NaBH₄ addition to the catalytic mixture.