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The study on the effect of fatty acid saturation on low-rank coal (LRC) flotation is still limited. In this investigation, density functional theory (DFT) combined with Zeta potential and Fourier transform infrared spectroscopy (FTIR) was used to study the mechanism of intermolecular weak interaction at the LRC-water interface of fatty acids (decanoic acid (DA), undecylenic acid (UA), and phenyl propionic acid (PA)) with different saturations and different dodecane (D) composition hydrocarbon oil-fatty acid mixed collectors (D-DA, D-UA, D-PA). The findings demonstrated that the hydrogen bond interaction and electrostatic interaction between the UA/PA with unsaturated bonded carbon chains and the LRC molecular fragments/water molecules were stronger than DA without a saturated bond carbon chain, and UA/PA strengthened its interaction with water molecules on the whole, even PA molecules would preferentially interact with water molecules. The unsaturated bond had a minimal impact on the adsorption of the LRC hydrophobic site, and the strength of the hydrogen bond between the mixed collector and LRC is D-DA > D-UA > D-PA. In the actual flotation process, the strong hydrogen bonding and electrostatic interaction between UA/PA and water molecules weaken the collection performance of the mixed collector D-UA/D-PA for LRC, which also confirmed the research results of DFT, FTIR, and Zeta.
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In this work, the assembly behavior and structure of a compound collector with different carboxyl group positions at the low-rank coal (LRC)-water interface were investigated through coarse-grained molecular dynamics simulation (CGMD) combined with sum-frequency vibration spectroscopy (SFG). The choice of compound collector was dodecane +decanoic acid (D-DA) and dodecane +2-butyl octanoic acid (D-BA). CGMD results showed that the carboxyl group at the carbon chain's middle can better control the assembly process between carboxylic acid and D molecules. SFG research found that the carboxyl group at the carbon chain's termination had a greater impact on the displacement of the methyl/methylene symmetric stretching vibration peak, while the carboxyl group at the carbon chain's middle had a greater impact on the displacement of the methyl/methylene asymmetric stretching vibration peak. The spatial angle calculation results revealed that the methyl group's orientation angle in the D-BA molecule was smaller and the carboxyl group's orientation angle in the BA molecule was bigger, indicating that D-BA spread more flatly on the LRC surface than D-DA. This meant that the assembled structure had a larger effective adsorption area on the LRC surface. The flotation studies also verified that the assembly behavior and structure of D-BA with the carboxyl group at the carbon chain's middle at the LRC-water interface were more conducive to the improvement of flotation efficiency. The study of interface assembly behavior and structure by CGMD combined with SFG is crucial for the creation of effective compound collectors.
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In this study, the calcium gangue material calcite (−10 µm) was used to investigate the effects of different kinds of metal ions and dosages on the dispersion behavior of calcite. The test results showed that the dispersion behavior of calcite was poor under strongly alkaline conditions without the addition of metal ions, and the reason for that was calcite dissolved ions. The degree of influence of different metal ions on calcite dispersion behavior was Fe3+ > Mg2+ > Na+. The three metal ion dosage tests showed that the dispersion behavior of calcite became poorer with the increase of metal ion dosage. This mainly showed that with the increase of Na+ dosage, the trend of the dispersion behavior of calcite was not obvious, but with the increase of Fe3+ and Mg2+ dosage, the trend of calcite dispersion behavior changed more. The dispersion behavior of calcite was devastated by 5 × 10−4 mol/L Fe3+ at pH = 4−12. The different mechanisms of the three metal ions were identified by zeta potential, solution chemistry, and XPS analysis. Na+ only changed the zeta potential value of the calcite surface, which acted as a compressed electric double layer. However, the formation of metal hydroxide species or metal hydroxide surface precipitation due to the adsorption of Fe3+ and Mg2+ on the mineral surface resulted in the change of the dispersion behavior of calcite.
Asunto(s)
Calcio , Minerales , Carbonato de Calcio , HidróxidosRESUMEN
The efficient dispersion of particles is a prerequisite for the efficient flotation of fine smithsonite. However, unavoidable ions (Ca2+) in the pulp have become a challenge for the efficient separation of fine smithsonite, due to the high content of pulp and small radius of hydrated ions. Therefore, the dispersion behavior and mechanism of Ca2+ action on smithsonite are important for improving the efficiency of smithsonite flotation. In this study, the effects of Ca2+ on the dispersion behavior of fine smithsonite were studied using a turbidity test. The results showed that the dispersion behavior of smithsonite was good in the absence of Ca2+ at a range of pH = 4−12. However, the measured turbidity values of smithsonite decreased with the addition of calcium ions. In particular, the dispersion behavior of smithsonite became worse at pH > 10. Zeta potential test results showed that the smithsonite's surface potential shifted positively, and the absolute value of potential decreased in the presence of Ca2+. The results of X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) analysis showed that calcium ions were adsorbed on the smithsonite surface, which may have caused ion exchange or the generation of calcium hydroxide precipitation leading to particle coalescence behavior. The calculations of solution chemistry and DLVO theory indicated that calcium ions adsorbed on the surface of smithsonite to form Ca(OH)+ or precipitation, which reduced the potential energy of interparticle interactions and led to the disruption of dispersion behavior of smithsonite.
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Calcio , Calcio/química , Iones , Microscopía Electrónica de Rastreo , Intercambio IónicoRESUMEN
The efficient filtration of low-rank coal (LRC) slurry was significantly beneficial to the production process of wet coal beneficiation. However, relatively few studies have been reported on novel pretreatment methods for the efficient filtration of LRC slurry. In this paper, the mechanism of ultrasonic pretreatment to promote flocculation and filtration of slurry was studied. The hydrophobic variation of the slurry surface was measured by contact angle and XPS. The flocculation properties of slurry were characterized using zeta potential and FBRM. The effects of filter cake porosity and ultrasonic pretreatment on slurry filtration resistance were calculated by L-F NMR and Darcy's theory. The results showed that the ultrasonic pretreatment promoted the flocculation and filtration performance of LRC slurry, increased the filtration rate, and decreased the cake moisture content. Meanwhile, the contact angle of LRC increased significantly from 50.1° to 67.8° after ultrasonic pretreatment, and the surface tension of the filtrate decreased from 69.5 to 53.31 mN/m. Ultrasonic pretreatment reduced the absolute value of the zeta potential of coal slurry from 24.8 to 21.0 mV, and the average chord length of flocs increased from 5-10 µm to 25-30 µm, thus weakening the electrostatic repulsion between coals to promote floc formation. In addition, the pore tests and filtration theory calculations showed that the ultrasonic pretreatment significantly improved the permeability of the filter cake to water and reduced the resistance to slurry during filtration. In particular, the mesopore porosity increased by 9.18%, and the permeability increased by 2.937 × 108 m2. Therefore, this contributed to the reduction of slurry filtration resistance. This research provides an efficient method for promoting the efficient filtration of slurry.
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It has been generally proved that mixed collectors can enhance the flotation of low-rank coal (LRC). However, the inhibition effect of mixed collectors on the detachment between particles and bubbles is still unclear. In this paper, the energy feature of air bubble detachment from the LRC surface in the presence of dodecane (D), oleic acid (OA), and the mixture of dodecane and oleic acid (OA-D) was studied. The effect of collectors on the LRC surface property was analyzed using contact angle measurement, X-ray photoelectron spectroscopy, and wetting heat measurement. The force and displacement during the detachment process were measured synchronously using microforce balance. The results showed that the collector treatment increased the C-C/C-H content and decreased the content of oxygen-containing groups on the LRC surface. The synergistic effect between OA and D enabled the mixed collector to exhibit higher contact angle and wetting heat. Bubble detachment from the LRC surface can be divided into two stages: bubble stretching and bubble sliding, which corresponded to activation energy and detachment work, respectively. The activation energy and detachment work decreased in the same order of OA-D > OA > D, indicating that the mixed collector OA-D increased the energy of bubble detachment from the LRC surface and enhanced the adhesion strength. The theoretical detachment work was calculated, and the calculated results were in agreement with the measured results. This research provides a new perspective on the mechanism of LRC flotation being improved by mixed collectors.
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Semi-industrial tests were conducted to investigate the feasibility and efficiency of a combined column and mechanical flotation cell process for the beneficiation of Sanshandao low-grade gold ore. The results showed that the performance of the combined flotation process of the cyclonic-static microbubble flotation column (FCSMC) and mechanical flotation cells was superior to that of the mechanical flotation cell, while the flowsheet was simplified. FCSMC is efficient when used on fine particles, whereas a mechanical flotation cell is effective for coarse particles. Thus, the combined flotation process exhibited a better separation performance by employing the strengths of both methods. The use of the combined FCSMC and cell flotation process showed promising results for a producing grade of 48.24 g/t gold with 96.13% recovery. The combined column and cell flotation process introduces a new approach for the separation of low-grade gold ore.
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Separating oxidized zinc minerals from flotation tailings is always a challenge. In this study, a flotation tailing from Wulagen zinc mine in China (Zn grade < 1%) was processed using froth flotation with combinations of amines (OPA 10, OPA 1214, OPA 13, DDA) and Na2S to study the effects of these amines on the zinc recovery as well as their interactions with other reagents, aiming to screen out a proper reagent scheme to improve zinc separation from extremely low-grade zinc flotation tailings. The results show that different amines led to different flotation performance, and the collectors were ranked as OPA 1214, OPA 13, OPA 10 and DDA in a decreasing order based on flotation collectivity and selectivity. An increase in the concentration of each collector increased the zinc recovery but reduced the concentrate zinc grade. Interactions were also observed between different amines and Na2S and Na2SiO3, and OPA 1214 outdid the others in saving the usage of both the Na2S and Na2SiO3. The measured adsorption of collector onto smithsonite was found to correlate well with flotation test results. It was concluded that hydrocarbon chains can be held accountable for the difference in the flotation performance with different amines. The longer the hydrocarbon chain, the stronger the hydrophobic association ability of amine, which is conducive to the selective amine adsorption onto sulfurized smithsonite particles and hence the smithsonite flotation.
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It is well known that mixed collectors can effectively strengthen the flotation of low-rank coal. However, less concern has been paid to the detachment of low-rank coal flotation using mixed collectors. In this study, the force of air bubble detachment from low-rank coal surface treated by oleic acid (OA), dodecane (D), and oleic acid-dodecane (OA-D) collector mixture was investigated using microforce balance. The results showed that the process of bubble detachment from the low-rank coal surface was divided into three stages: relaxation stage, stretching stage, and sliding stage. The equilibrium contact angle and critical contact angle were the transition points between different stages. The order of detachment force required for bubble detachment from the surface of low-rank coal was OA-D > OA > D, indicating a synergistic effect between OA and D. Based on the three parameters of equilibrium contact angle, critical contact angle, and contact line length, a theoretical model was proposed to calculate the detachment force. The calculated results were in agreement with the measured results.
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Thermal-sensitive polymers have been tested on settling, compacting or dewatering of clays or oil sand tailings. However, not much attention has been paid to explore the effect of temperature on flocculating performance using thermal-sensitive polymers. In this study, poly(NIPAM-co-DMAPMA) was synthesized and employed to investigate the flocculating and re-flocculating performance of hydrophilic and hydrophobic particles at two specific temperatures; meanwhile settling and dewatering behaviors were also investigated. The results demonstrated that good flocculating performances were achieved at both room temperature (â¼23 °C) and lower critical solution temperature (45 °C). Furthermore, larger flocs were formed at 45 °C as the copolymer was added. Floc strength and re-flocculating ability of the flocs were also intensified prominently at 45 °C. Additionally, settling and dewatering rates of suspensions were improved, and the moisture of filtered cakes was reduced when suspensions were at 45 °C. The phenomena could be justified by the phase transition of the copolymer from hydrophilicity to hydrophobicity as the temperature increased. There were much stronger adhesion forces between particles and higher adsorption amount of the copolymer onto solid surfaces at 45 °C. Therefore, the copolymer may be promising in solid-liquid separation to improve the floc size, floc strength, and settling and dewatering rate to achieve much lower moisture filtered cake.