Chemical and electrochemical basis of bioleaching processes

Citation
Gs. Hansford et T. Vargas, Chemical and electrochemical basis of bioleaching processes, HYDROMETALL, 59(2-3), 2001, pp. 135-145
Citations number
43
Categorie Soggetti
Metallurgy
Journal title
HYDROMETALLURGY
ISSN journal
0304386X → ACNP
Volume
59
Issue
2-3
Year of publication
2001
Pages
135 - 145
Database
ISI
SICI code
0304-386X(200102)59:2-3<135:CAEBOB>2.0.ZU;2-0
Abstract
The bioleaching of sulfide minerals involves electrochemical and chemical r eactions of the mineral with the leach liquor and the extra-cellular polysa ccharide layers on the microorganisms. The microorganism derive energy by o xidising the sulfur moiety and ferrous iron, which can be interpreted using electrochemistry and chemiosmotic theory. Recently, significant advances h ave been made in understanding the mechanism by which the bioleaching of su lfide minerals occurs. Kinetic models based on the proposed mechanism are b eing used successfully to predict the performance of continuous bioleach re actors. The measurement of oxygen and carbon dioxide consumption rates toge ther with the measurement of redox potentials has led to this further eluci dation of the mechanism of bioleaching of sulfide minerals and enabled the kinetics of the sub-processes involved to be determined separately. It has been shown that bioleaching involves at least three important sub-processes , viz., attack of the sulfide mineral, microbial oxidation of ferrous iron and some sulfur moiety. The overall process occurs via one of two pathways depending on the nature of the sulfide mineral, a pathway via thiosulfate r esulting in sulfate being formed or a polythionate pathway resulting in the formation of elemental sulfur. For the case of pyrite, the primary attack of the sulfide mineral is a chemical ferric leach producing ferrous iron. T he role of the bacteria is to re-oxidise the ferrous iron back to the ferri c form and maintain a high redox potential as well as oxidising the element al sulfur that is formed in some cases. The first two sub-processes of chem ical ferric reaction with the mineral and bacterial oxidation of the ferrou s iron are linked by the redox potential. The sub-processes are in equilibr ium when the rate of iron turnover between the mineral and the bacteria is balanced. Rate equations based on redox potential or ferric/ferrous-iron ra tio have been used to describe the kinetics of these sub-processes. The kin etics have been described as a function of the ferric/ferrous-iron ratio or redox potential which enables the interactions of the two sub-processes to be linked at a particular redox potential through the rate of ferrous iron turn-over. The use of these models in predicting bioleach behaviour for py rite is presented and discussed. The model is able to predict which bacteri al species will predominate at a particular redox potential in the presence of a particular mineral, and which mineral will be preferentially leached. The leach rate and steady state redox potential can be predicted from the bacterial to mineral ratio. The implications of this model on bioleach reac tor design and operation are discussed. Research on the chemistry and elect rochemistry of the ferric leaching of sulfide minerals and an electrochemic al mechanism for ferrous iron oxidation based on chemiosmotic theory will b e presented and reviewed. (C) 2001 Elsevier Science B.V. All rights reserve d.