Bacterial Leaching of Chalcopyrite Ore

Canfell, Anthony John (1999). Bacterial Leaching of Chalcopyrite Ore PhD Thesis, Chemical Engineering, University of Queensland.

Attached Files (Some files may be inaccessible until you login with your UQ eSpace credentials)
Name Description MIMEType Size Downloads
THE13237_PhD.pdf Full text application/pdf 5.06MB 0
n01front.pdf n01front.pdf application/pdf 1.30MB 17
n02chapter1-2.pdf n02chapter1-2.pdf application/pdf 422.82KB 14
n03chapter3-4.pdf n03chapter3-4.pdf application/pdf 2.53MB 16
n04chapter5a.pdf n04chapter5a.pdf application/pdf 1.64MB 13
n05chapter5b.pdf n05chapter5b.pdf application/pdf 1.84MB 18
n06chapter6.pdf n06chapter6.pdf application/pdf 1.17MB 14
n07chapter7-8.pdf n07chapter7-8.pdf application/pdf 253.49KB 11
n08References.pdf n08References.pdf application/pdf 148.84KB 10
n09appendices.pdf n09appendices.pdf application/pdf 143.51KB 10
Author Canfell, Anthony John
Thesis Title Bacterial Leaching of Chalcopyrite Ore
School, Centre or Institute Chemical Engineering
Institution University of Queensland
Publication date 1999
Thesis type PhD Thesis
Supervisor Professor Paul Greenfield
Subjects 771000 Mining Environments
270301 Bacteriology
Abstract/Summary Bacterial leaching utilises bacteria, ubiquitous to sulphide mining environments to oxidise sulphide ores. The sulphide mineral chalcopyrite is the most common copper mineral in the world, comprising the bulk of the known copper reserves. Chalcopyrite is resistant to bacterial leaching and despite research over the last 20-30 years, has not yet been economically bioleached. Attempts have been made to use silver to catalyse the bacterial leaching of chalcopyrite since the early seventies. The majority of reported testwork had been performed on finely ground ore and concentrates in agitated batch reactors. This project used silver to catalyse the bioleaching of chalcopyrite in shake flasks, small columns and large columns. The catalytic effect was extensively studied and experimental parameters were varied to maximise copper recovery. Silver was also used to catalyse the ferric leaching of chalcopyrite at elevated temperatures. It was noted that the leaching performance of chalcopyrite in shake flasks compared to columns was markedly different. The specific differences between shake flasks and columns were qualified and separately tested to determine which parameter(s) affected the bioleaching of chalcopyrite. It was found that the ore to solution ratio, aeration, addition of carbon dioxide, solution distribution and small variations in the leaching temperature did not significantly effect the bioleaching of chalcopyrite ore in columns. The method of silver addition to columns did significantly affect the overall copper extraction. The ore in shake flasks was subjected to abrasion between ore particles and with the base of the flask. A test was designed to mimic the shake flask conditions, without the abrasion. The low abrasion test performed similarly to a column, operated with optimum silver addition. This indicated that the inherent equipment difference between shake flask and column operation largely accounted for the difference in leaching performance. Chalcopyrite ore was biologically leached in large columns. The ore crush size and other conditions were typical of those used in the field. The biological leach achieved 65% copper extraction in 160 days. This level of copper extraction is significantly higher than any previously reported results (typically /10% copper extraction) and represents a significant advance in the bacterial leaching of chalcopyrite ore. Due to the inherent high temperature within underground stopes, it was decided to investigate the possibility of separating the leaching and the bacterial oxidation stages. The concept of separate bacterial and ferric leaching has been previously suggested, however the application to a stope, and heat exchange between the process streams was a novel approach. Large column ferric leaches at 70 oC illustrated the technical feasibility of this process. Copper extraction was rapid and high (70% in 100 days of leaching), even when a reduced level of silver catalysis was used. After leaching in large columns, samples of ore were taken for analysis by optical mineralogy. The analysis gave valuable insights into the nature of reaction passivation on chalcopyrite ore. In particular, it was discovered that the precipitation of goethite was a major limiting factor in the bioleaching and ferric leaching of chalcopyrite in columns. In addition, reduced sulphide species were detected on the surface of residual chalcopyrite, giving an indication of the sequential nature of the chalcopyrite reaction chemistry. The bacterial population was characterised using DNA techniques developed during the project. Qualitative speciation was carried out and compared between the columns, down the columns and over time in a column. Comparison of these populations enabled greater mechanistic understanding of the role of bacteria in the leaching of chalcopyrite. This work was the most comprehensive attempt to date made to delineate the complex microbiological/mineral actions using analysis of population dynamics from a mixed inoculum. It was found that the iron oxidiser Thiobacillus ferrooxidans dominated within the columns and leach solutions. The sulphur oxidiser Sulfobacillus thermosulfidooxidans was also prevalent in the columns, particularly during the period of rapid chalcopyrite oxidation. The high temperature, ferric leaching of chalcopyrite was unexpectedly poor in the first round of large columns. The reason for the low extraction was attributed to an increase in pH down the column, resulting in excessive goethite precipitation. The solution flowrate (velocity) was increased by ten times in subsequent columns. There were no operational problems (e.g. break-up of ore agglomerates). The increase in flowrate resulted in a high yield of copper. The kinetics of extraction were faster than a corresponding bacterial leach, confirming the potential advantage of a high temperature leach. The small column studies highlighted that it was important to get an even distribution of silver down the stope to enable maximum catalytic effect. If the ore were agglomerated, silver would be added with acid at that point. However, it may not always be possible to agglomerate the ore. For example, the process may be used in-situ on a fractured ore body, or on an ore that has a low fines content, and hence does not require agglomeration. Various complexing agents were tested for their ability to distribute silver at the start of the leach and to recover silver at the end of the leach. For instance when silver was complexed with thiourea and then trickled through the ore, an even distribution of silver was achieved. After leaching was completed, a thiourea wash recovered a significant amount of the silver. These two techniques minimised the amount of silver required and thus significantly added to the economic viability of the process. The success of the technical work has led to an evaluation of the process in the field. A flowsheet was developed for the high temperature, in-stope ferric leach of chalcopyrite. An economic analysis was performed that illustrated the process would be viable in certain situations. An engineering study considered issues such as acid consumption, aeration, silver distribution, silver recovery and a heat balance of the stope.
Keyword Chalcopyrite

Citation counts: Google Scholar Search Google Scholar
Created: Fri, 21 Nov 2008, 17:42:52 EST