In this work, the active sites and species involved in xanthate adsorption on sphalerite/marmatite surfaces were studied using adsorption capacity measurements, single mineral flotation, and time-of-flight secondary ion mass spectrometry (ToF-SIMS) analysis. The effects of Fe concentration on the xanthate adsorption capacity, Cu activation, and the flotation response of sphalerite/marmatite were determined. A discovery was that xanthate can interact with Fe atoms in the crystal of sphalerite/marmatite, as well as with Zn and Cu on the surface. We detected C₂S₂⁻ fragment ions from dixanthogen, and dixanthogen may have been adsorbed on the surface of marmatite. The amounts of Cu and copper xanthate adsorbed on the marmatite surface were lower than those on the sphalerite surface, because Fe occupies Cu and Zn exchange sites. These results help to address the long-standing controversy regarding the products and mechanisms of xanthate adsorption on Fe-bearing sphalerite surfaces.

In order to explore the commercialized applications of the low-grade bauxite in the refractory industry, a calcination integrated with acid leaching method was adopted to remove the potassium (K) and iron (Fe) from the diaspore-illite (DI) type low-grade bauxite. Following calcining the bauxite at different temperatures, the leaching parameters, including the sulfuric acid concentration, temperature, sulfuric acid to bauxite ratio, and reaction time were systematically studied. The appropriate and economical conditions for removing the impurities were found to be calcining the bauxite at 550 °C, and leaching it with a sulfuric acid solution of 1.2 mol/L, sulfuric acid/bauxite ratio of 9 mL/g at a reaction temperature of 70 °C and reaction time of 2 h, under these conditions, the removal efficiency of K and Fe from the bauxite can reach 30.32% and 47.33%, respectively. The treated bauxite was examined by XRD analysis, SEM observations, and chemical analysis. Kinetics of the removing process were calculated by two models, and the results showed that the leaching process was controlled by the mixed shrinking core model, which was affected by both the diffusion through solid layer and the interface transfer. In summary, the approach in this work presents a promising process for comprehensive utilization of the low-grade bauxite.

A series of impact compression tests were conducted to study the breakage characteristics of magnetite, as well as the impact pressure on its strain rate and dynamic compressive strength. The dynamic mechanical properties and fragmentation size distribution of magnetite under diverse impact loads and cyclic impact were investigated, with fractal theory as a basis and split Hopkinson pressure bar (SHPB). Breakage methods were also employed to analyze the fracture morphology of magnetite. According to the result, the fractal dimension can reflect the distribution of fragments in various sizes. If the strain rate increases, the fractal dimension will be larger, the fragment size will be finer, and the fragmentation degree will be more influential. A micro-analysis of SEM images demonstrates that the fracture morphology is determined by mineral properties. Under low load cyclic impact, intergranular fracture is the main fractography. Besides, the intergranular fracture will be changed to a transgranular one as the impact load increases.

This paper presents the development of an environmentally friendly, small molecular depressant citrus pectin for improving the recovery of cassiterite resources. Citrus pectin extracted from citrus peel was utilized as the depressant, and it demonstrated significant potential in separating calcite from cassiterite in micro-flotation tests. The molecular weight of the citrus pectin extracted in this paper decreased from 11,485,412 Da to 32,959 Da compared to commercial pectin, resulting in the depressant efficiency of the reagent. The results of a zeta potential and adsorption test indicated that citrus pectin had less and weaker adsorption on the cassiterite surface and could be replaced with NaOL. The chemical adsorption process of citrus pectin on the surface of calcite was determined through FTIR spectroscopy analysis. XPS analysis results indicated that the interaction between the carboxyl groups of citrus pectin and calcium atoms enables adsorption to occur. The AFM revealed that citrus pectin displayed a uniform and dense pattern of point-like adsorption on the surface of calcite. Micro-flotation experiments showed that cassiterite recovery of 80% can be obtained at a citrus pectin dosage of 10 mg/L. Citrus pectin has the advantages of being low-cost, highly selective, and environmentally suitable, making it a promising alternative to conventional reagents.