Flotation kinetics of molybdenite in common sulfate salt solutions

被引:14
作者
Zhu, Hongjia [1 ]
Li, Yubiao [1 ,2 ]
Lartey, Clement [1 ]
Li, Wanqing [1 ]
Qian, Gujie [2 ]
机构
[1] Wuhan Univ Technol, Sch Resources & Environm Engn, Wuhan 430070, Hubei, Peoples R China
[2] Flinders Univ S Australia, Coll Sci & Engn, Adelaide, SA 5042, Australia
基金
中国国家自然科学基金;
关键词
Molybdenite; Flotation; Kinetics; Sulfate salt; HIGH SALINITY; CHALCOPYRITE; SEAWATER; COAL; FLOATABILITY; CATIONS; PYRITE; ROLES;
D O I
10.1016/j.mineng.2020.106182
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This study investigates the kinetics of molybdenite (MoS2) flotation in sulfate media (Na+, K+, Ca2+ and Mg2+) with a concentration of 10(-4)-10(-2) M. Results indicate that both monovalent and divalent cations inhibit MoS2 flotation. Three flotation models were used to fit the flotation kinetic data. The Gamma model gives the best goodness of fit in terms of R-Adj(2) (adjusted coefficient of determination) and RMSE (root mean square error), however, fails in predicting MoS2 flotation recovery in MgSO4 solution due to the contradictory to the actual flotation trend. In contrast, the rectangular model fits MoS2 flotation in all the sulfate solutions. The flotation rate constant k values decrease with increasing sulfate concentration, indicating that the increased sulfate concentration reduces MoS2 flotation rate. The lowest k was found in the MgSO4 media, suggesting that MgSO4 is most detrimental to MoS2 flotation recovery. In addition, the R-infinity was decreased with increasing sulfate concentration in an order of Mg2+ > Ca-2+ > K+ > Na+, with the minimum R-infinity being obtained in 10(-2) M MgSO4, probably due to the formation and adsorption of hydrophilic Mg(OH)(2) onto MoS2 surface.
引用
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页数:5
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