Based on the mineralogical characterization for the polymetallic sulfide ore, the way to improve silver recovery was studied. The results showed that silver was the most valuable metal whose grade was 448.82 g/t Ag, w...Based on the mineralogical characterization for the polymetallic sulfide ore, the way to improve silver recovery was studied. The results showed that silver was the most valuable metal whose grade was 448.82 g/t Ag, while 0.118% Cu, 1.65% Pb and 1.06% Zn may be comprehensively utilizated. The main silver-bearing minerals were argent and aregentite which accounted for 87.18% of total silver. Argentite and other metal minerals were distributed in the gangue minerals in complex forms. Argentite grains of 33.76% minus 50 μm indicated that a fine grinding scheme was necessary to enhance the degree of dissociation, and meanwhile selective grinding must be considered to prevent a complete grinding of coarse grains. The optimum regrinding fineness in the Cu flotation was determined as 73% minus 37 μm, while grains of 68.5% minus 74 μm in one-stage grinding remained unchanged as much as possible. Consequently, silver recovery increased to 2.68%, as well as the content of Pb simultaneously decreased from 7.26% to 2.68% in the Cu concentrate. From the lead pyrometallurgical point of view, recovering larger amounts of silver and lead at the expense of decreasing the grade of lead to a suitable level is not only economically viable for the plant, but also convenient for subsequent processing. Silver and lead recovery increased to 13.18% and 12.58%, respectively, while the Pb grade decreased from 53.1% to 46.12% for the Pb concentrate.展开更多
Investigations were carried out, on a low grade siliceous iron ore sample by magnetic separation, to establish its amenability for physical beneficiation. Mineralogical studies revealed that the sample consists of mag...Investigations were carried out, on a low grade siliceous iron ore sample by magnetic separation, to establish its amenability for physical beneficiation. Mineralogical studies revealed that the sample consists of magnetite, hematite and goethite as major opaque oxide minerals where as silicates as well as carbonates form the gangue minerals in the sample. Processes involving combination of classification, dry magnetic separation and wet magnetic separation were carried out to upgrade the low grade siliceous iron ore sample to make it suitable as a marketable product. The sample was first ground and each closed size sieve fractions were subjected to dry magnetic separation and it was observed that limited upgradation is possible. The ground sample was subjected to different finer sizes and separated by wet low intensity magnetic separator. It was possible to obtain a magnetic concentrate of 67% Fe by recovering 90% of iron values at below 200 lm size.展开更多
Ultrafine barium hexaferrite(BaFe12O19) powders were synthesized from the metallurgical extracts of low-grade Egyptian barite ore via a co-precipitation route. Hydrometallurgical treatment of barite ore was systemat...Ultrafine barium hexaferrite(BaFe12O19) powders were synthesized from the metallurgical extracts of low-grade Egyptian barite ore via a co-precipitation route. Hydrometallurgical treatment of barite ore was systematically studied to achieve the maximum dissolution efficiency of Fe(~99.7%) under the optimum conditions. The hexaferrite precursors were obtained by the co-precipitation of BaS produced by the reduction of barite ore with carbon at 1273 K and then dissolved in diluted HCl and FeCl3 solution at pH 10 using NaOH as a base; the product was then annealed at 1273 K in an open atmosphere. The effect of Fe^3+/Ba^2+ molar ratio and the addition of hydrogen peroxide(H2O2) on the phase structure, crystallite size, morphology, and magnetic properties were investigated by X-ray diffraction, scanning electron microscopy, and vibrating sample magnetometry. Single-phase BaFe(12)O(19) powder was obtained at an Fe^3+/Ba^2+ molar ratio of 8.00. The formed powders exhibited a hexagonal platelet-like structure. Good maximum magnetization(48.3 A×m^2×kg^–1) was achieved in the material prepared at an Fe^3+/Ba^2+ molar ratio of 8.0 in the presence of 5% H2O2 as an oxidizer and at 1273 K because of the formation of a uniform, hexagonal-shaped structure.展开更多
基金Funded by the National Natural Science Foundation of China(No.51374247)
文摘Based on the mineralogical characterization for the polymetallic sulfide ore, the way to improve silver recovery was studied. The results showed that silver was the most valuable metal whose grade was 448.82 g/t Ag, while 0.118% Cu, 1.65% Pb and 1.06% Zn may be comprehensively utilizated. The main silver-bearing minerals were argent and aregentite which accounted for 87.18% of total silver. Argentite and other metal minerals were distributed in the gangue minerals in complex forms. Argentite grains of 33.76% minus 50 μm indicated that a fine grinding scheme was necessary to enhance the degree of dissociation, and meanwhile selective grinding must be considered to prevent a complete grinding of coarse grains. The optimum regrinding fineness in the Cu flotation was determined as 73% minus 37 μm, while grains of 68.5% minus 74 μm in one-stage grinding remained unchanged as much as possible. Consequently, silver recovery increased to 2.68%, as well as the content of Pb simultaneously decreased from 7.26% to 2.68% in the Cu concentrate. From the lead pyrometallurgical point of view, recovering larger amounts of silver and lead at the expense of decreasing the grade of lead to a suitable level is not only economically viable for the plant, but also convenient for subsequent processing. Silver and lead recovery increased to 13.18% and 12.58%, respectively, while the Pb grade decreased from 53.1% to 46.12% for the Pb concentrate.
文摘Investigations were carried out, on a low grade siliceous iron ore sample by magnetic separation, to establish its amenability for physical beneficiation. Mineralogical studies revealed that the sample consists of magnetite, hematite and goethite as major opaque oxide minerals where as silicates as well as carbonates form the gangue minerals in the sample. Processes involving combination of classification, dry magnetic separation and wet magnetic separation were carried out to upgrade the low grade siliceous iron ore sample to make it suitable as a marketable product. The sample was first ground and each closed size sieve fractions were subjected to dry magnetic separation and it was observed that limited upgradation is possible. The ground sample was subjected to different finer sizes and separated by wet low intensity magnetic separator. It was possible to obtain a magnetic concentrate of 67% Fe by recovering 90% of iron values at below 200 lm size.
基金financially supported by the Science and Technology Development Fund (STDF), Egypt (Grant No.Project ID 246)
文摘Ultrafine barium hexaferrite(BaFe12O19) powders were synthesized from the metallurgical extracts of low-grade Egyptian barite ore via a co-precipitation route. Hydrometallurgical treatment of barite ore was systematically studied to achieve the maximum dissolution efficiency of Fe(~99.7%) under the optimum conditions. The hexaferrite precursors were obtained by the co-precipitation of BaS produced by the reduction of barite ore with carbon at 1273 K and then dissolved in diluted HCl and FeCl3 solution at pH 10 using NaOH as a base; the product was then annealed at 1273 K in an open atmosphere. The effect of Fe^3+/Ba^2+ molar ratio and the addition of hydrogen peroxide(H2O2) on the phase structure, crystallite size, morphology, and magnetic properties were investigated by X-ray diffraction, scanning electron microscopy, and vibrating sample magnetometry. Single-phase BaFe(12)O(19) powder was obtained at an Fe^3+/Ba^2+ molar ratio of 8.00. The formed powders exhibited a hexagonal platelet-like structure. Good maximum magnetization(48.3 A×m^2×kg^–1) was achieved in the material prepared at an Fe^3+/Ba^2+ molar ratio of 8.0 in the presence of 5% H2O2 as an oxidizer and at 1273 K because of the formation of a uniform, hexagonal-shaped structure.