8 resultados para rhodochrosite

em Digital Commons - Montana Tech


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Manganese is commonly known to be a metal of great strategic importance. It is essential in the production of all steels, first as a scavenger to remove oxygen and sulfur, and second as an alloying element in wear-resis­tant steels.

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With the increasing importance of manganese in the metallurgical fields of today and tomorrow, ex­tensive work along the lines of its successful ex­ploitation has been accomplished by many investiga­tors. Since tie current world situation has shut off most of our supply of high-grade manganese ores from foreign sources, the low-grade domestic deposits have entered the fields of investigation very rapidly.

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Although there are many uses for manganese today, none of them approaches its importance as a deoxidizing agent in the manufac­ture of steels. Without manganese the steelmaking in­dustry would be very seriously handicapped. The metal­lurgy of manganese has been developed around the high-grade ores, and unfortunately, our reserves of high-grade ores are very limited.

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It is estimated that 90 to 95% of the world’s consumption of manganese is used in the steel industry in the form of either ferromanganese or spiegeleisen. The remainder is used in the form of either salts or oxides, chloride, dioxide and monoxide.

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The Continental porphyry Cu‐Mo mine, located 2 km east of the famous Berkeley Pit lake of Butte, Montana, contains two small lakes that vary in size depending on mining activity. In contrast to the acidic Berkeley Pit lake, the Continental Pit waters have near-neutral pH and relatively low metal concentrations. The main reason is geological: whereas the Berkeley Pit mined highly‐altered granite rich in pyrite with no neutralizing potential, the Continental Pit is mining weakly‐altered granite with lower pyrite concentrations and up to 1‐2% hydrothermal calcite. The purpose of this study was to gather and interpret information that bears on the chemistry of surface water and groundwater in the active Continental Pit. Pre‐existing chemistry data from sampling of the Continental Pit were compiled from the Montana Bureau of Mines and Geology and Montana Department of Environmental Quality records. In addition, in March of 2013, new water samples were collected from the mine’s main dewatering well, the Sarsfield well, and a nearby acidic seep (Pavilion Seep) and analyzed for trace metals and several stable isotopes, including dD and d18O of water, d13C of dissolved inorganic carbon, and d34S of dissolved sulfate. In December 2013, several soil samples were collected from the shore of the frozen pit lake and surrounding area. The soil samples were analyzed using X‐ray diffraction to determine mineral content. Based on Visual Minteq modeling, water in the Continental Pit lake is near equilibrium with a number of carbonate, sulfate, and molybdate minerals, including calcite, dolomite, rhodochrosite (MnCO3), brochantite (CuSO4·3Cu(OH)2), malachite (Cu2CO3(OH)2), hydrozincite (Zn5(CO3)2(OH)6), gypsum, and powellite (CaMoO4). The fact that these minerals are close to equilibrium suggests that they are present on the weathered mine walls and/or in the sediment of the surface water ponds. X‐Ray Diffraction (XRD) analysis of the pond “beach” sample failed to show any discrete metal‐bearing phases. One of the soil samples collected higher in the mine, near an area of active weathering of chalcocite‐rich ore, contained over 50% chalcanthite (CuSO4·5H2O). This water‐soluble copper salt is easily dissolved in water, and is probably a major source of copper to the pond and underlying groundwater system. However, concentrations of copper in the latter are probably controlled by other, less‐soluble minerals, such as brochantite or malachite. Although the acidity of the Pavilion Seep is high (~ 11 meq/L), the flow is much less than the Sarsfield Well at the current time. Thus, the pH, major and minor element chemistry in the Continental Pit lakes are buffered by calcite and other carbonate minerals. For the Continental Pit waters to become acidic, the influx of acidic seepage (e.g., Pavilion Seep) would need to increase substantially over its present volume.

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The contents of this paper represent attempts to deposit the metal, manganese from sodium manganate solutions. The source of manganese was limited to the nodulized product from roasting rhodochrosite and was therefore chiefly manganese oxide.

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The manganese minerals occur in the peripheral zone of the Butte district with quartz in veins, which at depth contain galena and sphalerite closely associated with silver-bearing minerals. The manganese oxides are all oxidation products formed by weathering of primary rhodochrosite or rhodonite.

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The beneficiation of rhodochrosite ore to the extent that it is suitable for nodulizing and subsequent use in the steel industry is intriguing. Such ores from certain mines is relatively easy to beneficiate, but the rhodo-chrosite ore from several deposits of the Philipsburg district has never been successfully up-graded by any of the several known beneficiating methods.