RESUMEN
Adsorption of electrolytes (ions) at solid-liquid interfaces alters the physical and chemical properties of materials and hence plays a critical role in manufacturing and processing of nanomaterials featuring large surface or interfacial areas of desired structures and morphology. Many experiments and theoretical calculations using various electrical double layer (EDL) models have been conducted to understand how and where ions adsorb at charged surfaces in a liquid. However, conclusions from previous research remain inconclusive because of model-dependent approaches to studying ion adsorption at diverse solid-liquid interfaces. In this study, atomic force microscopy is used to image in liquids the surface lattice structure of two kaolinite basal planes in the presence and absence of monovalent and divalent cations. Distinct adsorption of ions through different mechanisms (such as electrostatic attraction and specific adsorption) is identified through atomic resolution imaging without the assumption of an EDL structure.
RESUMEN
HYPOTHESIS: The self-assembly of platy clay particles is influenced by anisotropic surface charging properties of the particles. The Stern potentials of particle surfaces are controlled by solution pH. Consequently, the energy-favorable particle association varies with pH, leading to different self-assembly structures. Therefore, it should be possible to form desired nanostructure of final clay product through self-assembly of clay particles by controlling the surface charge through adjusting solution pH. EXPERIMENTS: Three different surfaces of kaolinite clay nanoparticles were selectively exposed for Stern potential determination using an atomic force microscope. Aggregation structures through particle self-assembly were predicted based on the analysis of interaction energies between various types of surfaces of kaolinite particles. The structures were visually confirmed using the freeze-dried scanning electron microscopy technique. FINDINGS: By reducing pH of a concentrated kaolinite suspension from 8 to 5 and 3, the dispersed kaolinite particles were self-assembled to a well-stacked configuration and card-house structure, respectively. Current study demonstrates that the pH-dependent surface properties of platy kaolinite nanoparticles can be successfully used to understand the macroscopic behavior (rheology) of kaolinite nanoparticle suspensions and design nanostructures of clay products (catalysts and sorbents). The pH-dependent self-assembly is also applicable to other platy particles of anisotropic surface (charging or wettability) properties.
RESUMEN
In this paper, a novel flotation technique that combines nano-scale bubbles generated by hydrodynamic cavitation (HC) and carrier flotation is proposed to promote the flotation efficiency of a high-ash (43%) ultra-fine coal sample (<45 µm). We investigated the mechanism by which cavitation bubbles enhance the separation efficiency of carrier flotation using focused beam reflectance measurements, polarizing microscopy, and extended Derjaguin-Landau-Verwey-Overbeek theory. The carrier particles (polystyrene (PS)) and fine coal were pre-treated in a venturi tube and then floated in a laboratory mechanical flotation cell. The flotation results indicate that the presence of cavitation bubbles significantly improved the carrier flotation performance of high-ash ultra-fine coal. This improvement was attributed to the presence of highly hydrophobic PS, which creates additional gas nuclei in the flotation system. The nano-bubbles, which were produced by the venturi tube and adhered to the fine coal particle surfaces, were conducive to the agglomeration of fine coal particles into large aggregates. Moreover, the nano-bubbles functioned as "bridges" of interaction between the carrier particles and large aggregates of fine coal particles. This paper mainly focused on the effect of carrier (PS) and HC on high-ash fine coal. The influence of different HC intensities on carrier (PS) flotation was discussed. Two models for the interactions between the coal particles, nano-bubbles, and PS during cavitation were proposed and were proved using the E-DLVO theory.
RESUMEN
For the purpose of understanding the colloidal behaviors of illite in mineral processing, probing the surface charging property of illite is of great significance. This research explored the edge and basal surfaces of illite using an atomic force microscope (AFM). The interaction forces between Si/Si3N4 probes and illite edge/basal surfaces were measured, respectively, at different pH values in 10 mM KCl solutions. Theoretical Derjaguin-Landau-Verwey-Overbeek forces were matched up with the measured forces to derive the surface potentials of the two surfaces. On the illite basal surface, an attractive force occurred at pH 3.0, while repulsive forces dominated from pH 5.0 to 10.0. On the illite edge surface, a slight attractive force was also obtained at pH 3.0. However, the interaction changed into repulsion at pH 5.0, and this repulsive force increased gradually from pH 6.0 to 10.0. Illite basal and edge surfaces were both negatively charged, but the basal surface exhibited more negative charges than the edge surface from pH 3.0 to 10.0. Increasing solution pH from 3.0 to 10.0, there was no detection of the point of zero charge (PZC) of the illite basal surface; however, the PZC of the illite edge surface should have occurred at a pH slightly lower than 3.0. This is the first time that surface potentials of illite edge and basal surfaces were attained separately by direct force measurements. These findings provide insights into the colloidal behaviors of illite in mineral processing and oil sands extraction.
