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Synthetic Sulfide Concentrate Dissolution Kinetics in HNO3 Media

Authors :
Oleg Dizer
Kirill Karimov
Aleksei Kritskii
Denis Rogozhnikov
Source :
Materials; Volume 15; Issue 22; Pages: 8149
Publication Year :
2022
Publisher :
Multidisciplinary Digital Publishing Institute, 2022.

Abstract

The nature of tennantite (Cu12As4S13), chalcopyrite (CuFeS2) and sphalerite (ZnS) particles’ mixture dissolution in nitric acid (HNO3) media was investigated in this study. The effects of temperature (323–368 K), HNO3 (1–8 mol/L) and Fe3+ (0.009–0.036 mol/L) concentrations, reaction time (0–60 min) and pyrite (FeS2) additive (0.5/1–2/1; FeS2/sulf.conc.) on the conversion of the minerals were evaluated. It has been experimentally shown that the dissolution of the mixture under optimal conditions (>353 K; 6 mol/L HNO3; FeS2/synt. conc = 1/1) allows Cu12As4S13, CuFeS2 and ZnS conversion to exceed 90%. The shrinking core model (SCM) was applied for describing the kinetics of the conversion processes. The values of Ea were calculated as 28.8, 33.7 and 53.7 kJ/mol, respectively, for Cu12As4S13, CuFeS2 and ZnS. Orders of the reactions with respect to each reactant were calculated and the kinetic equations were derived to describe the dissolution rate of the minerals. It was found that the interaction between HNO3 solution and Cu12As4S13, CuFeS2 and ZnS under the conditions investigated in this are of a diffusion-controlled nature. Additionally, the roles of Fe(III) in the initial solution and FeS2 in the initial pulp as catalysts were studied. The results indicated that the increase in Fe3+ concentration significantly accelerates the dissolution of the mixture, while the addition of FeS2 forms a galvanic coupling between FeS2, and Cu12As4S13 and CuFeS2, which also accelerates the reaction rate. The results of the study are considered useful in developing a hydrometallurgical process for polymetallic sulfide raw materials treatment.

Details

Language :
English
ISSN :
19961944
Database :
OpenAIRE
Journal :
Materials; Volume 15; Issue 22; Pages: 8149
Accession number :
edsair.doi.dedup.....94847869ca7495c804bd9aeb28fc0fef
Full Text :
https://doi.org/10.3390/ma15228149