The hydration film on particle surface plays an important role in bubble-particle adhesion in mineral flotation process. The thicknesses of the hydration films on natural hydrophobic coal and hydrophilic mica surfaces...The hydration film on particle surface plays an important role in bubble-particle adhesion in mineral flotation process. The thicknesses of the hydration films on natural hydrophobic coal and hydrophilic mica surfaces were measured directly by atomic force microscopy (AFM) based on the bending mode of the nominal constant compliance regime in AFM force curve in the present study. Surface and solid-liquid interfacial energies were calculated to explain the forming mechanism of the hydration film and atomic force microscopy data. The results show that there are significant differences in the structure and thickness of hydration films on coal and mica surfaces. Hydration film formed on mica surface with the thickness of 22.5 nm. In contrast, the bend was not detected in the nominal constant compliance regime. The van der Waals and polar interactions between both mica and coal and water molecules are characterized by an attractive effect, while the polar attractive free energy between water and mica (-87.36 mN/m) is significantly larger than that between water and coal (-32.89 mN/m), which leads to a thicker and firmer hydration layer on the mica surface. The interfacial interaction free energy of the coal/water/bubble is greater than that of mica. The polar attractive force is large enough to overcome the repulsive van der Waals force and the low energy barrier of film rupture, achieving coal particle bubble adhesion with a total interfacial free energy of-56.30 mN/m.展开更多
The surface states of pyrite(Fe S2) were theoretically investigated using first principle calculation based on the density functional theory(DFT). The results indicate that both the(200) and(311) surfaces of pyrite un...The surface states of pyrite(Fe S2) were theoretically investigated using first principle calculation based on the density functional theory(DFT). The results indicate that both the(200) and(311) surfaces of pyrite undergo significant surface atom relaxation after geometry optimization, which results in a considerable distortion of the surface region. In the normal direction, i.e., perpendicular to the surface, S atoms in the first surface layer move outward from the bulk, while Fe atoms move toward the bulk, forming an S-rich surface. The surface relaxation processes are driven by electrostatic interaction, which is evidenced by a relative decrease in the surface energy after surface relaxation. Such a relaxation process is visually interpreted through the qualitative analysis of molecular mechanics. Atomic force microscopy(AFM) analysis reveals that only sulfur atom is visible on the pyrite surface. This result is consistent with the DFT data. Such S-rich surface has important influence on the flotation properties of pyrite.展开更多
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...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.展开更多
基金Project(2014BAB01B03)supported by the National Key Technology R&D Program During the 12th Five-Yean Plan of ChinaProject(51774286)supported by the National Natural Science Foundation of ChinaProject(BK20150192)supported by the Natural Science Foundation of Jiaaagsu Province,China
文摘The hydration film on particle surface plays an important role in bubble-particle adhesion in mineral flotation process. The thicknesses of the hydration films on natural hydrophobic coal and hydrophilic mica surfaces were measured directly by atomic force microscopy (AFM) based on the bending mode of the nominal constant compliance regime in AFM force curve in the present study. Surface and solid-liquid interfacial energies were calculated to explain the forming mechanism of the hydration film and atomic force microscopy data. The results show that there are significant differences in the structure and thickness of hydration films on coal and mica surfaces. Hydration film formed on mica surface with the thickness of 22.5 nm. In contrast, the bend was not detected in the nominal constant compliance regime. The van der Waals and polar interactions between both mica and coal and water molecules are characterized by an attractive effect, while the polar attractive free energy between water and mica (-87.36 mN/m) is significantly larger than that between water and coal (-32.89 mN/m), which leads to a thicker and firmer hydration layer on the mica surface. The interfacial interaction free energy of the coal/water/bubble is greater than that of mica. The polar attractive force is large enough to overcome the repulsive van der Waals force and the low energy barrier of film rupture, achieving coal particle bubble adhesion with a total interfacial free energy of-56.30 mN/m.
基金Project(51464029)supported by the National Natural Science Foundation of ChinaProject(2014M562343)supported by China Postdoctoral Science FoundationProject(KKSY201421110)supported by the Scholar Development Project of Yunnan Province,China
文摘The surface states of pyrite(Fe S2) were theoretically investigated using first principle calculation based on the density functional theory(DFT). The results indicate that both the(200) and(311) surfaces of pyrite undergo significant surface atom relaxation after geometry optimization, which results in a considerable distortion of the surface region. In the normal direction, i.e., perpendicular to the surface, S atoms in the first surface layer move outward from the bulk, while Fe atoms move toward the bulk, forming an S-rich surface. The surface relaxation processes are driven by electrostatic interaction, which is evidenced by a relative decrease in the surface energy after surface relaxation. Such a relaxation process is visually interpreted through the qualitative analysis of molecular mechanics. Atomic force microscopy(AFM) analysis reveals that only sulfur atom is visible on the pyrite surface. This result is consistent with the DFT data. Such S-rich surface has important influence on the flotation properties of pyrite.
基金Project(2004CB619204) supported by the National Basic Research Program of ChinaProject(2002) supported by the Teaching and Research Award Program for Outstanding Young Teachers in Higher Education Institutions, China
文摘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.
