Extended DLVO theory applied to coal slime-water suspensions

Coal slimes are mainly composed of coal and clay particles.The interaction energies among these particles were calculated using extended DLVO(DERJAGUIN-LANDAU-VERWEY-OVERBEEK)theory and the aggregation mechanisms were analyzed based on the settling experiments for coal-kaolinite and coal-montmorillonite suspensions,respectively,under different conditions of water hardness.The results indicate that for coal-kaolinite suspensions,as the water hardness reaches 10.0mol/L,the coal particles aggregate with each other easily,and then,the coal particles may aggregate with kaolinite particles.However,no aggregation occurs between kaolinite particles.A clay platelet network is formed in coal-montmorillonite suspensions by montmorillonite particles and coal particles are captured into the network.Coal and montmorillonite particles settle completely.

Interactions between bubble and particles of key minerals of diasporic bauxite through the extended DLVO theory

The flotation of diasporic bauxite is to separate diaspore(valuable mineral)from aluminosilicate minerals(gangue minerals,mainly including kaolinite,illite and pyrophyllite),and the microscopic interaction force between the two types of minerals and air bubbles determines the separation efficiency.In this paper,based on the extended Derjaguin-Landau-Verwey-Overbeek(DLVO)theory,the van der Waals,electrostatic and hydrophobic interaction between particles of the four minerals mentioned above and air bubbles in collectorless solution were calculated first,and then diaspore and kaolinite were taken as examples to analyze the influence of various factors such as electrolyte concentration,mineral particle size,air bubble size,collector type(dodecylamine hydrochloride(DAH)and sodium oleate(NaOL))and concentration,and pulp pH on the interactions between the particles of valuable mineral and gangue minerals and air bubbles.The results showed that the total extended DLVO interactions between the four minerals and air bubbles were repulsive in most cases in collectorless solution.The increase in electrolyte concentration reduced the interaction force or even changed the direction of the force under certain circumstances.The addition of DAH and NaOL can reduce the adhesion energy barrier of kaolinitebubble and diaspore-bubble respectively.Each type of minerals exhibited a specific interface interaction response with air bubbles in each collector with different pH values.The research results have theoretical guiding significance for the optimization and directional control of diasporic bauxite flotation conditions.

EXTENDED DLVO THEORY AND ITS APPLICATION IN COAL SLURRY SUSPENSION

Not only the basic principle of the extended DLVO has been expounded, but also all kinds of interaction energies between fine particles in coal slurry suspension have been calculated in this peper. Coal is a natural hydrophobic mineral, and the hydrophobic attractive power between coal surfaces is a decisive factor to the aggregation of particles in hydrophobic suspensions. The calculation results show that the extended DLVO theory can explain successfully the coagulation or dispersion of fine particle coal.

A stepwise approach to enhancing flotation of low-grade zinnwaldite through the cationic/DL-2-octanol/anionic reagent combinations: Behavior and mechanism analysis

In order to alleviate the pressure on the supply of lithium resources, this research proposes the use of binary/ternary collectors with high selectivity and collecting ability to enhance the flotation purification of low-grade zinnwaldite ore. The binary collector is a mixture of dodecylamine polyoxyethylene ether and DL-2-octanol. A binary collector is added first, followed by sodium oleate, known as a ternary collector. Under acidic conditions, the recovery of Li2O in the concentrate was increased by 8.26% with the binary collector and 13.70% with the ternary collector, compared to the dodecylamine polyoxyethylene ether. The binary collector enhanced the dispersibility of the single collector, while co-adsorption strengthened the hydrophobic nature of the zinnwaldite surface. Consequently, zinnwaldite particles,after the application of binary collector, displayed inter-particle flocculation and attachment to bubbles within 60×10^(-9)m compared to other particles. Ternary collector exhibited the capacity to lower critical micelle concentration and surface tension, subsequently inducing a denser and thicker hydrophobic layer through electrostatic forces, hydrophobic interactions, and chemical reactions. The objective of this research is to facilitate the recovery of lithium resources from low-grade ores in order to meet the needs of sustainable development.

Shear hydrophobic flocculation and flotation of ultrafine Anshan hematite using sodium oleate

Effects of stirring speed and time, pH and sodium oleate concentration on the shear hydrophobic flocculation of ultrafine Anshan hematite with sodium oleate as the surfactant were discussed. The results show that these parameters significantly affect the shear hydrophobic flocculation of ultrafine hematite. The optimum conditions for the flocculation are： stirring speed 1 400 r/min, flocculation time 20 min, pH 9 and sodium oleate concentration 3.94×10-4 mol/L; the flotation recovery of hematite flocs is remarkably high compared with non flocculated ultrafine hematite. According to the extended DLVO theory, the total interaction potential of Anshan ultrafine hematite was determined. The calculation results indicate that the hydrophobic flocculation state of the ultrafine hematite-sodium oleate system is mainly dominated by electric double layer repulsive interaction potential and hydrophobic interaction potential. A mechanical agitation is required to impart particles a kinetic energy to overcome potential barrier between them due to the existence of electric double layer repulsive interaction potential. Those particles further approach to form flocs due to the significant increase of the hydrophobic interaction potential.

Interfacial interaction of bio-leaching of pyrite mineral

Electrokinetic and contact angle measurements were used to discuss the interfacial interaction on bio-leaching of pyrite mineral. Surface energy parameters of pyrite mineral and thiobacillus ferrooxidans were obtained by calculating according to formula of Young＇s equation and contact angle measurements. The results show that surface energy of thiobacillus ferrooxidans is much higher than that of pyrite mineral, and the reaction of pyrite mineral with thiobacillus ferrooxidans causes the reduction of the pyrite surface energy. The interfacial interaction energies between pyrite mineral and thiobaciUus ferrooxidans were also obtained based on polar interfacial interaction theory and electrokinetic and contact angle measurements. The thermodynamics approach only considering Lifshitz-van der Waals and Lewis acid-base interaction fails to explain the adhesion behavior of the bacteria, but the extended Derjaguin-Landan-Verwey-Overbeek theory concerning Lifshitz-van der Waals and Lewis acid-base and the electrostatic can exactly predict interfacial interaction.

Dispersion of ultrafine alumina in modifier solution ——the role of polar interfacial interaction

Dispersion of ultrafine alumina suspension is examined by using particle size analyzer. The zeta potential and contact angle measurements were used to discuss the electrokinetic behavior and surface wettability of alumina in modifier solution, and to calculate the electrostatic interaction forces and interfacial interaction forces between alumina particles. The aggregation of ultrafine alumina occurs near its PZC. Addition of modifier increases the zeta potential of alumina and its surface hydrophilicity, resulting in increase of electrostatic and hydration repulsion. It makes the suspension of ultrafine alumina completely dispersed. The average particle size of the suspension is decreased from 1.73 μm in absence of modifier to 0.8 μm in the presence of tripolyphosphate. According to polar interfacial interaction approach, the hydration forces responsible for the stability of alumina suspension in the presence of modifier have also been obtained. The extended DLVO theory is successful to describe the dispersion behavior of ultrafine alumina in modifier solution.