Dissolution Behavior of Non-Ferrous Smelter Slag in Aqueous Solution of Sulphur Dioxide

Canadian Institute of Mining, Metallurgy and Petroleum
Shamia Hoque Charles Q. Jia
Organization:
Canadian Institute of Mining, Metallurgy and Petroleum
Pages:
18
File Size:
3059 KB
Publication Date:
Jan 1, 2004

Abstract

Smelter slags contain valuable metals such as Co, Ni and Cu in proportions of less than 1 wt% along with about 40 wt% of Fe and 15 wt% of Si. Although aqueous SO2 is a versatile lixiviant for transition metals, dissolving the slag in aqueous SO2 produces solutions in which Co and Ni concentrations are lower than that of Fe due to the low metal/ Fe ratio in the slag. To develop the options for increasing Co and Ni concentrations the solubility of slag in aqueous SO2 was studied experimentally and theoretically using OLI, a software package for simulating electrolytes chemistry. The modeling results correlated well with experimental results. The model suggested that the species dominating the system was FeSO3, which would precipitate out as FeSO3.3H2O when the concentration of Fe+2 reached 1.22 molal and the concentration of S032- was beyond 1.4 molal. In the experiments the influence of pH and solids loading were studied. The leach solution obtained after dissolution of slag at 50% solids loading had a pH of 1.85. On raising the pH to 3, precipitation occurred. Analysis of the solution collected after the addition of alkali showed over 50% reduction of Fe, Co and Ni. XRD analysis revealed the precipitate to be of amorphous nature due to the silica present. The analysis confirmed that the precipitate was mainly FeSO3.3H2O. The paper also discusses the potential impact of the slag on the environment.
Citation

APA: Shamia Hoque Charles Q. Jia  (2004)  Dissolution Behavior of Non-Ferrous Smelter Slag in Aqueous Solution of Sulphur Dioxide

MLA: Shamia Hoque Charles Q. Jia Dissolution Behavior of Non-Ferrous Smelter Slag in Aqueous Solution of Sulphur Dioxide. Canadian Institute of Mining, Metallurgy and Petroleum, 2004.

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