2009
DOI: 10.1016/j.hydromet.2008.08.004
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Study in reduction-roast leaching manganese from low-grade manganese dioxide ores using cornstalk as reductant

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Cited by 130 publications
(46 citation statements)
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“…The objective of this stage of the process is reducing MnO 2 in presence of a reductant agent, SO 2 (g) (other reducing reagents have been used in treating manganese ores, such as oxalic acid, hydrogen peroxide and glucose [15], cornstalk [16], phenols [17], cane molasses [19], CaS [20], carbon [23] or waste tea [34]) and obtaining a solution of MnSO 4 (aq) to be sent to the neutralization stage, and then to electrolysis. The mixed leaching allows for recovering almost all of the manganese of the anodic lodes and scrapings (95% is supposed in the calculations).…”
Section: Sulphation At Low Temperature (50 • C)mentioning
confidence: 99%
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“…The objective of this stage of the process is reducing MnO 2 in presence of a reductant agent, SO 2 (g) (other reducing reagents have been used in treating manganese ores, such as oxalic acid, hydrogen peroxide and glucose [15], cornstalk [16], phenols [17], cane molasses [19], CaS [20], carbon [23] or waste tea [34]) and obtaining a solution of MnSO 4 (aq) to be sent to the neutralization stage, and then to electrolysis. The mixed leaching allows for recovering almost all of the manganese of the anodic lodes and scrapings (95% is supposed in the calculations).…”
Section: Sulphation At Low Temperature (50 • C)mentioning
confidence: 99%
“…The development of processes to recover low-grade manganese ores and other secondary sources has taken emphasis in the last decades as the manganese demand has grown rapidly [12,13], and the depletion of high manganese ore sources. Several processes have been studied to recover low grade manganese ores (20-30% Mn) by using different methods: leaching of manganese carbonate in ammonium sulfate solution [14]; recovery of manganese from electric arc furnace dust of ferromanganese by using sulfuric acid as leaching agent, and oxalic acid, hydrogen peroxide, and glucose as reducing reagents [15]; reduction-roasting of low-grade manganese dioxide ores by using sulfuric acid as leaching solvent and cornstalk as reducing reagent [16]; sulfuric acid leaching of ocean manganese nodules using phenols as reducing agents [17]; sulfur-based reduction roasting-acid leaching of low-grade manganese oxide ores [18]; reductive leaching of low-grade manganese ores, using cane molasses as reducing reagent and sulfuric acid as solvent [19]; reduction-acid leaching of low grade manganese ores using CaS as reductant [20]; recovery of manganese from spent batteries [21]; reuse of anode slime from the zinc electrolysis [22]; and, recovering manganese from treated sludge of the exhaust gases of ferroalloy production furnaces [23].…”
Section: Introductionmentioning
confidence: 99%
“…Only poor targets could be achieved for the high similarity in density and magnetic susceptibility of manganese and iron minerals. Additionally, their extremely fine, but intergrowth occurrence state, also obstructs the effective beneficiation [10][11][12]. Reduction-leaching processes are proposed to recover manganese from manganese oxide ores [10][11][12][13][14].…”
Section: Introductionmentioning
confidence: 99%
“…[8][9][10][11][12][13][14] The results have shown that these biomass wastes can reduce manganese oxide of the ore at temperatures below 600 °C with a degree of reduction of more than 95 %. For example, Cheng et al 8 has reported that low-grade manganese dioxide ores can be totally reduced by biomass cornstalk at 500 °C.…”
Section: Introductionmentioning
confidence: 99%
“…[8][9][10][11][12][13][14] The results have shown that these biomass wastes can reduce manganese oxide of the ore at temperatures below 600 °C with a degree of reduction of more than 95 %. For example, Cheng et al 8 has reported that low-grade manganese dioxide ores can be totally reduced by biomass cornstalk at 500 °C. Yang 11 and Long 9 found that low-grade pyrolusite can be reduced Moreover, biomass reduction is a zero emission processes, because the amount of CO 2 released during the reduction process is equal to that absorbed during biomass growth.…”
Section: Introductionmentioning
confidence: 99%