In this work, a mineralogical study and thermal decomposition analysis of jarosite residue sample from a zinc plant were carried out. The mineralogical analysis showed that the jarosite residue is mainly composed of four components, including jarosites, sulfates–hydroxides, sulfides and spinel. The distribution of relevant metallic elements in these components was characterized using a sequential extraction process. The X-ray diffraction results showed that AFe₃(OH)₆(SO₄)₂ and ZnFe₂O₄ are the main components of the jarosite residue sample. The thermal decomposition mechanisms of ammoniojarosite and sodium jarosite were studied by TG-DSC (Thermogravimetric analysis–differential scanning calorimetry). The thermal decomposition process and the corresponding mechanism of the jarosite residue were analyzed. The jarosite thermal decomposition process includes the removal of crystal water, dihydroxylation and deammoniation, desulfonation of component jarosite and desulfonation of component zinc sulfate.

The resource utilization of cyanide tailings has significant environmental and economic benefits. The efficient recovery of gold from low-grade cyanide tailings containing 1.71 g/t Au was performed by a chlorination roasting–flotation process. The effects of roasting temperature, calcium chloride, internal coke, external coke, copper sulfide concentrate, and kaolin on the recovery rate of concentrate, gold grade, and sorting efficiency were investigated. The optimized process parameters were as follows: 16 wt% calcium chloride dihydrate, 6 wt% internal carbon, 1 wt% external carbon, 9 wt% copper sulfide concentrate, 2 wt% kaolin, and roasting temperature of 730 °C. The sorting rate, gold grade, and recovery rate of gold concentrate can reach 88.48%, 33.46 g/t, and 76.7%, respectively, and the gold grade of tailings was as low as 0.17 g/t. In the matte phase, gold can be enriched in the form of gold grains. Therefore, through chlorination roasting, the trapped gold can be released and deposited on the surface of the matte phase due to the transformation from hematite to magnetite. The gold-deposited metal sulfide can be effectively recycled through flotation. These results have potential guiding significance for the efficient recovery of gold from cyanide tailings.

In this study, a method for determining the lead components in waste lead paste was proposed, using simulated and spent lead paste as research objects. To compare the effectiveness of different determining methods, we selected three methods for comparison and investigated the reasons for measurement deviation. The results indicate that the measurement deviation in the current method primarily stems from the following three factors: (1) Pb is soluble in an acetic acid solution under certain conditions; (2) Pb and PbO₂ undergo redox reactions; and (3) hydrogen peroxide can undergo redox reactions with Pb. It is feasible to determine the lead content using the kinetic rules of Pb and PbO₂ in the acetic acid-hydrogen peroxide system. The method of determination proposed in this paper is as follows. Firstly, lead dioxide is dissolved in hydrogen peroxide under acidic conditions. Subsequently, the concentration of lead dioxide is determined, and the quantity of hydrogen peroxide consumed is recorded. Then, a new sample is taken, and the lead oxide is dissolved in an acetic acid solution. The concentration of lead oxide is determined using the EDTA·2Na titration method. The residue of lead sulfate in the filtrate is dissolved in a sodium chloride solution, and its concentration is determined using the EDTA·2Na titration method. Based on the previously recorded volume of hydrogen peroxide, the remaining lead dioxide in the residue is dissolved in a mixture of acetic acid and hydrogen peroxide. The remaining lead dioxide is then removed from the new sample employing kinetic principles. Finally, the residual metallic lead in the sample is dissolved in a nitric acid solution, and its concentration is determined using the EDTA·2Na titration method.

Ultrasound is introduced into the gold adsorption process by activated carbon to improve the adsorption efficiency. The effects of ultrasonic equipment, initial pH value, amount of activated carbon, initial CN⁻ concentration, and temperature on the Au(CN${)}_2^{-}$ adsorption onto activated carbon were investigated. The adsorption results show that the water bath ultrasonic generator is more beneficial to promote the gold adsorption onto activated carbon than the probe ultrasonic equipment. With the introduction of ultrasound, the gold adsorption capacity of activated carbon is obviously improved, and the gold balance loading is increased by about 37%. The Freundlich model can describe well the adsorption behavior of Au(CN${)}_2^{-}$ onto activated carbon with or without ultrasound, which indicates that the Au(CN${)}_2^{-}$ adsorption onto activated carbon belongs to multi-molecular chemisorption. Compared with the pseudo-first-order equation and intra-particle diffusion equation, the pseudo-second-order equation can better fit dynamic data. Through X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), infrared spectroscopy (FT-IR), BET specific surface area, SEM, and particle size distribution analysis, it is proved that the enhancement of the gold adsorption onto activated carbon by ultrasound is due to the continuous action of ultrasound, which reduces the particle size and ultrasonication increases specific surface area through physical fragmentation effects and improves active site accessibility by reducing mass transfer resistance of activated carbon, rather than changing the adsorption mechanism of gold onto activated carbon.

As a metallurgical solid waste rich in active calcium oxide, magnesium slag (MS) is endowed with significant carbon dioxide sequestration potential due to its inherent properties, providing a feasible path for the simultaneous solution of waste residue disposal and carbon dioxide emission reduction. However, current research has neither clarified the kinetic mechanism (core theoretical support for carbon dioxide sequestration industrialization) nor systematically evaluated the life cycle environmental impacts of MS’s two carbonation routes (direct or indirect leaching carbonation). To address this, this study explores kinetic laws via the single-factor control variable method, and combines life cycle assessment (LCA) to fill the gap, providing key theoretical support for process optimization and engineering promotion. Kinetic results show indirect carbon dioxide sequestration (ICDS) forms an inert silicon-rich layer (core-shrinkage model, mixed control, 28.4 kJ/mol activation energy), while direct carbon dioxide sequestration (DCDS) involves dual-layer formation and pore blockage (mixed control, 14.0 kJ/mol). The ICDS achieves a higher reaction rate of 89%, compared to 63% for the DCDS. In life cycle assessments, DCDS demonstrates outstanding overall environmental sustainability, particularly excelling in carbon dioxide sequestration and acidification control, while ICDS exhibits significant environmental drawbacks (such as high carbon dioxide emissions and ecological toxicity). However, ICDS possesses advantages such as high feedstock utilization and strong synthesis capabilities for high-value-added products. Through targeted optimization, its environmental indicators can be reduced in the future, making it suitable for specific scenarios like high-end calcium carbonate production and resource utilization of low-grade magnesium slag.

As a pioneering exploration of gallium nitride (GaN) as reinforcement in metal matrix composites, this study systematically investigated the mechanical–electrical property evolution in copper matrix composites through controlled GaN incorporation—a research gap scarcely addressed previously. GaN-Cu composites with tailored GaN contents were successfully synthesized by precisely controlled mechanical alloying and powder metallurgical processing and exhibited exceptional mechanical–electrical synergies. Advanced microstructural characterization via X-ray diffraction and electron microscopy revealed the homogeneous dispersion of GaN nanoparticles within the Cu matrix, forming coherent interfacial structures. The characterization results show that GaN-Cu composites could be successfully prepared by mechanical alloying and powder metallurgy methods, and it was confirmed that GaN nanoparticles could improve the mechanical properties of metal matrix composites as reinforcement; with an exponential increase in GaN content, the decrease in conductivity became very slow. With an increase in GaN content, the electrical conductivity decreased in an “L” shape, while the hardness first increased and then decreased, but the hardness could reach up to 128.66 HV, which is about 130% higher than that of the substrate.