Common rare earth(RE) minerals, such as bastnasite and monazite, may be formed in deposits associated with carbonate gangue, such as calcite and dolomite. Sodium oleate is a widely used collector for the flotation of ...Common rare earth(RE) minerals, such as bastnasite and monazite, may be formed in deposits associated with carbonate gangue, such as calcite and dolomite. Sodium oleate is a widely used collector for the flotation of both RE and gangue minerals, which might, therefore, be an inefficient process due to the lack of selectivity of this collector. Since these minerals are also sparingly soluble in solution, they could release their constituent ions into the solution, which could affect the floatability of other minerals. In this study, the interactions of sodium oleate with bastnasite and monazite in the presence of dissolved dolomite species have been investigated. Microflotation tests were carried out to explore the effects of these dissolved species on the floatability of the RE minerals. Zeta potential measurements and XPS characterization were carried out to understand how the species affect the collector adsorption. To complement these characterizations, density functional theory(DFT) simulations were conducted to investigate the collector-mineral and collector-adsorbed species(on the mineral surface) interactions.The results show that collector-dolomite interaction energy is greater than that of collector-adsorbed species, but lower than collector-monazite interaction energy, explaining the decrease in the minerals' recovery upon exposure to the dissolved mineral species. It is also shown that oleate ions(OI^-) have the strongest interaction with the minerals compared to other oleate species such as acid soap(HOI_2^-) and oleate dimer(OI_2^(2-)). The behavior(strength and selectivity) of sodium oleate towards RE minerals and dolomite, as compared to other RE mineral collectors(such as aromatic hydroxamate), is attributed mainly to the collector's and the minerals' structure. The long hydrocarbon chain of sodium oleate which imparts hydrophobic characteristic to the minerals, makes it stronger collector than benzohydroxamate.Moreover, sodium oleate(with linear structure), unlike the aromatic hydroxamate, can approach the mineral easier due to lesser steric hindrance effect and higher reactivity of 0 involved in the interaction,making it less selective. In addition, it can interact easily with dolomite due to the presence of more exposed active sites than RE minerals.展开更多
Common collectors for rare earth mineral(REM) flotation,which include carboxylates and hydroxamates,face problems such as being non-selective and sensitive to impurity ions.A type of ionic liquid(IL),tetraethylammoniu...Common collectors for rare earth mineral(REM) flotation,which include carboxylates and hydroxamates,face problems such as being non-selective and sensitive to impurity ions.A type of ionic liquid(IL),tetraethylammonium mono-(2-ethylhexyl)2-ethylhexyl phosphonate([N_(2222)][EHEHP]),has been investigated previously for rare earth elements(REE) solvent extraction,and was proven to be selective and effective.In this work,[N_(2222)][EHEHP] was evaluated as a collector in bastnasite(a primary REM source for REE production) flotation for the first time.The results were compared with quartz and hematite,two common gangue minerals in REM deposits.Zeta potential measurements and Fouriertransform infrared spectroscopy(FT-IR) were completed to investigate the surface chemical properties involved in the flotation of these minerals using this collector.The findings were compared with microflotation results.FT-IR and zeta potential measurements suggest adsorption of the collector’s phosphonate group onto bastnäsite and hematite,likely through chemisorption;whereas for quartz,the minimum micro flotation recovery is likely due to no adsorption of IL on its surface.Micro flotation re sults show higher collectability of [N_(2222)] [EHEHP] for hematite than bastnasite,the latter only shows appreciable recovery at pH 5 with elevated dosage of IL(500 g/t).To achieve better separation,a two-stage flotation scheme was designed and evaluated by bench scale flotation on a synthetic mineral mixture.The concentrates and tails were analyzed by magnetic separation,and it is found that bastnasite recovery over 90% with maximum upgrade ratio 1.7 can be achieved with elevated collector dosage.展开更多
基金supported by the Natural Sciences and Engineering Research Council of Canada(NSERC)and Niobec,a Magris Resources Company through the Collaborative Research and Development Program(CRDPJ 453164-13)
文摘Common rare earth(RE) minerals, such as bastnasite and monazite, may be formed in deposits associated with carbonate gangue, such as calcite and dolomite. Sodium oleate is a widely used collector for the flotation of both RE and gangue minerals, which might, therefore, be an inefficient process due to the lack of selectivity of this collector. Since these minerals are also sparingly soluble in solution, they could release their constituent ions into the solution, which could affect the floatability of other minerals. In this study, the interactions of sodium oleate with bastnasite and monazite in the presence of dissolved dolomite species have been investigated. Microflotation tests were carried out to explore the effects of these dissolved species on the floatability of the RE minerals. Zeta potential measurements and XPS characterization were carried out to understand how the species affect the collector adsorption. To complement these characterizations, density functional theory(DFT) simulations were conducted to investigate the collector-mineral and collector-adsorbed species(on the mineral surface) interactions.The results show that collector-dolomite interaction energy is greater than that of collector-adsorbed species, but lower than collector-monazite interaction energy, explaining the decrease in the minerals' recovery upon exposure to the dissolved mineral species. It is also shown that oleate ions(OI^-) have the strongest interaction with the minerals compared to other oleate species such as acid soap(HOI_2^-) and oleate dimer(OI_2^(2-)). The behavior(strength and selectivity) of sodium oleate towards RE minerals and dolomite, as compared to other RE mineral collectors(such as aromatic hydroxamate), is attributed mainly to the collector's and the minerals' structure. The long hydrocarbon chain of sodium oleate which imparts hydrophobic characteristic to the minerals, makes it stronger collector than benzohydroxamate.Moreover, sodium oleate(with linear structure), unlike the aromatic hydroxamate, can approach the mineral easier due to lesser steric hindrance effect and higher reactivity of 0 involved in the interaction,making it less selective. In addition, it can interact easily with dolomite due to the presence of more exposed active sites than RE minerals.
基金Project supported by the Natural Sciences and Engineering Research Council of Canada(NSERC)Avalon Advanced Materials Inc.through the Collaborative Research and Development(CRD)Program(CRDPJ 44537-12)。
文摘Common collectors for rare earth mineral(REM) flotation,which include carboxylates and hydroxamates,face problems such as being non-selective and sensitive to impurity ions.A type of ionic liquid(IL),tetraethylammonium mono-(2-ethylhexyl)2-ethylhexyl phosphonate([N_(2222)][EHEHP]),has been investigated previously for rare earth elements(REE) solvent extraction,and was proven to be selective and effective.In this work,[N_(2222)][EHEHP] was evaluated as a collector in bastnasite(a primary REM source for REE production) flotation for the first time.The results were compared with quartz and hematite,two common gangue minerals in REM deposits.Zeta potential measurements and Fouriertransform infrared spectroscopy(FT-IR) were completed to investigate the surface chemical properties involved in the flotation of these minerals using this collector.The findings were compared with microflotation results.FT-IR and zeta potential measurements suggest adsorption of the collector’s phosphonate group onto bastnäsite and hematite,likely through chemisorption;whereas for quartz,the minimum micro flotation recovery is likely due to no adsorption of IL on its surface.Micro flotation re sults show higher collectability of [N_(2222)] [EHEHP] for hematite than bastnasite,the latter only shows appreciable recovery at pH 5 with elevated dosage of IL(500 g/t).To achieve better separation,a two-stage flotation scheme was designed and evaluated by bench scale flotation on a synthetic mineral mixture.The concentrates and tails were analyzed by magnetic separation,and it is found that bastnasite recovery over 90% with maximum upgrade ratio 1.7 can be achieved with elevated collector dosage.