Process mineralogy as a key factor affecting the flotation kinetics of copper sulfide mineralsShow others and affiliations
2019 (English)In: International Journal of Minerals, Metallurgy and Materials, ISSN 1674-4799, E-ISSN 1869-103X, Vol. 26, no 4, p. 430-439Article in journal (Refereed) Published
Abstract [en]
The aim of this study is to apply process mineralogy as a practical tool for further understanding and predicting the flotation kinetics of the copper sulfide minerals. The minerals’ composition and association, grain distribution, and liberation within the ore samples were analyzed in the feed, concentrate, and the tailings of the flotation processes with two pulp densities of 25wt% and 30wt%. The major copper-bearing minerals identified by microscopic analysis of the concentrate samples included chalcopyrite (56.2wt%), chalcocite (29.1wt%), covellite (6.4wt%), and bornite (4.7wt%). Pyrite was the main sulfide gangue mineral (3.6wt%) in the concentrates. A 95% degree of liberation with d80 > 80 µm was obtained for chalcopyrite as the main copper mineral in the ore sample. The recovery rate and the grade in the concentrates were enhanced with increasing chalcopyrite particle size. Chalcopyrite particles with a d80 of approximately 100 µm were recovered at the early stages of the flotation process. The kinetic studies showed that the kinetic second-order rectangular distribution model perfectly fit the flotation test data. Characterization of the kinetic parameters indicated that the optimum granulation distribution range for achieving a maximum flotation rate for chalcopyrite particles was between the sizes 50 and 55 µm.
Place, publisher, year, edition, pages
Springer, 2019. Vol. 26, no 4, p. 430-439
Keywords [en]
microscopic analysis, flotation, kinetics, second order rectangular distribution model, sulphide minerals
National Category
Metallurgy and Metallic Materials
Research subject
Mineral Processing
Identifiers
URN: urn:nbn:se:ltu:diva-73642DOI: 10.1007/s12613-019-1733-9ISI: 000464703200004Scopus ID: 2-s2.0-85064340474OAI: oai:DiVA.org:ltu-73642DiVA, id: diva2:1304863
Note
Validerad;2019;Nivå 2;2019-04-15 (svasva)
2019-04-152019-04-152020-08-26Bibliographically approved