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Surface heterogeneity of minerals can significantly affect the adsorption of collectors. Petroleum sulfonate is widely used as a fluorite collector, but how the surface heterogeneity of fluorite influences the adsorption of alkyl sulfonates remains unknown. Herein, two kinds of surface heterogeneity situations, i.e., edge and (1 1 1) _vacancy, were modeled, and the adsorption of sodium dodecyl sulfonate on them was simulated. The results show that the stable adsorption configuration of sodium dodecyl sulfonate on the edge was in a bridged mode, and the stable interaction configuration with vacancy was in a tridentate mode. The 2p orbit of fluorine on the surface of the edge and the vacancy could hinder collector adsorption. After adsorption, the 3d orbit of calcium interacted with the collector orbit above Fermi level, and moved towards the lower energy level, benefiting the adsorption process. It was also found that the adsorption intensity/strength of alkyl sulfonate on fluorite was directly proportional to the interaction intensity of the collector with the 3d orbits of calcium ions on the surface and vacancy. Therefore, the rough fluorite surface had a stronger adsorption effect on the collector, and the existence of vacancy could improve the surface adsorption energy, and thus enhance the adsorption of the collector on the fluorite surface. The rough fluorite surface requires high collector concentration to achieve saturated monolayer adsorption, so increasing vacancy was the better choice to improve the adsorption capacity of alkyl sulfonate on the fluorite surface. This study provides novel insights into the flotation mechanism, in the context of surface heterogeneity, and could guide the design of high-performance collectors for fluorite ore flotation. [ABSTRACT FROM AUTHOR]

Quartz powder (QP) is an inorganic filler that is expected to significantly enhance the dielectric and mechanical properties of epoxy (EP)-based composites applied in copper clad laminates and epoxy molding compounds for 5G applications. As is well-known, the performance of the QP–EP composites is directly correlated with the dispersion effect and the compatibility of QP with an EP matrix. Herein, we propose the surface modification method of QP by mixing SCAs of different alkyl chain lengths that contain amino and carbonyl groups. Different characterization methods (FTIR, TGA, XPS, SEM, contact angle measurement, viscosity, and mechanical properties) and molecular dynamics simulation were adopted to study its effect and mechanism. Through dual SCA modification, the viscosity of QP–EP composites was reduced by 11.70%, and the flexural and tensile strengths increased by 16.89% and 30.01%, respectively. In addition, it was revealed that the superiority of dual SCAs originated from the synergistic effect between APTES and SPIS, it was the electrostatic repulsion force between the amino groups of the two SCAs that caused a steric hindrance that activated the steric stabilization effect of SPIS, thus resulting in better dispersion and excellent compatibility. Meanwhile, the amino and carbonyl groups of the SCA interacted with the EP matrix via chemical bonds and hydrogen bonds, thus strengthening the interfacial adhesion between the QP and EP matrix and improving the mechanical performance of QP–EP composites. These results are evidence of the potential of the proposed approach, which is based on the synergistic compounding of SCA with different molecular structures, in powder industrial applications. [ABSTRACT FROM AUTHOR]

This investigation aims to demonstrate the effects of hydrophobic tails on the affinity and relevant flotation response of sulfonate-based collectors for fluorite. For this purpose, a series of alkyl sulfonates with different hydrophobic tails, namely sodium decanesulfonate (C10), sodium dodecylsulfate (C12), sodium hexadecanesulfonate (C16), and sodium dodecylbenzenesulfonate (C12B) were applied. The flotation tests showed that C12 and C12B had a better collecting performance than C10 and C16 at pH < 10, and the flotation recovery of fluorite was higher when adopting C12B as a collector compared with C12 with a strong base. The adsorption behaviors of collectors on the fluorite surface were studied through zeta potential, Fourier transform infrared (FTIR), and X-ray photoelectron spectroscopy (XPS) analyses. It was found that the affinity of alkyl sulfonates for fluorite was enhanced with the increase of the alkyl chain length from C10 to C16. The existence of phenyl in the hydrophobic tail of sulfonates could improve its activity for fluorite by reducing its surface tension. The abnormal phenomenon C16 with a high affinity for fluorite had a low collecting performance for fluorite mainly due to its overlong alkyl chain, resulting in low solubility in pulp, which restrained its interaction with fluorite. We concluded that C12B was the most applicable collector for fluorite among these reagents due to its high activity, high solubility, and low cost, which was further substantiated by calculating their molecular frontier orbital energy. [ABSTRACT FROM AUTHOR]