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Bioleaching is the extraction of specific metals from their ores through the use of bacteria. Bioleaching is one of several applications within biohydrometallurgy.
Bioleaching is a technique used by the mining industry to extract minerals such as gold and copper from their ores. Traditional extractions involve many expensive steps such as roasting and smelting, which require sufficient concentrations of elements in ores and are environmentally unfriendly. Low concentrations are not a problem for bacteria because they simply ignore the waste which surrounds the metals, attaining extraction yields of over 90% in some cases. These microorganisms actually gain energy by breaking down minerals into their constituent elements. The company simply collects the ions out of the solution after the bacteria have finished.
Some advantages associated with bioleaching are:
Some disadvantages associated with bioleaching are:
Currently it is more economical to smelt copper ore rather than to use bioleaching, since the concentration of copper in its ore is generally quite high. The profit obtained from the speed and yield of smelting justifies its cost. However, the concentration of gold in its ore is generally very low. The lower cost of bacterial leaching in this case outweighs the time it takes to extract the metal.
Additional recommended knowledge
The extraction of gold from its ore can involve numerous ferrous and sulfur oxidizing bacteria, including Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans (formerly known as Thiobacillus). For example, bacteria catalyse the breakdown of the mineral arsenopyrite (FeAsS) by oxidising the sulfur and metal (in this case arsenic ions) to higher oxidation states whilst reducing dioxygen by H2 and Fe3+. This allows the soluble products to dissolve.
This process actually occurs at the cell membrane of the bacteria. The electrons pass into the cells and are used in biochemical processes to produce energy for the bacteria to reduce oxygen molecules to water.
In stage 2, bacteria oxidise Fe2+ to Fe3+ (whilst reducing O2).
They then oxidise the metal to a higher positive oxidation state. With the electrons gained, they reduce Fe3+ to Fe2+ to continue the cycle.
The gold is now separated from the ore and in solution.
The process for copper is very similar. The mineral chalcopyrite (CuFeS2) follows the two stages of being dissolved and then further oxidised, with Cu2+ ions being left.
Extraction from mixture
Copper (Cu2+) ions are removed from the solution by ligand exchange solvent extraction which leaves other ions in the solution. The copper is removed by bonding to a ligand, which is a large molecule consisting of a number of smaller groups each possessing a lone pair. The ligand is dissolved in an organic solvent such as kerosene and shaken with the solution producing this reaction:
The ligand donates electrons to the copper, producing a complex - a central metal atom (copper) bonded to 2 molecules of the ligand. Because this complex has no charge, it is no longer attracted to polar water molecules and dissolves in the kerosene, which is then easily separated from the solution. Because the initial reaction is reversible, it is determined by pH. Adding concentrated acid reverses the equation, and the copper ions go back into an aqueous solution.
Then the copper is passed through an electro-winning process to increase its purity: an electric current is passed through the resulting solution of copper ions. Because copper ions have a 2+ charge, they are attracted to the negative cathodes and collect there.
The copper can also be concentrated and separated by displacing the copper with Fe from scrap iron:
The electrons lost by the iron are taken up by the copper. Copper is the oxidising agent (it accepts electrons), and iron is the reducing agent (it loses electrons).
Traces of precious metals such as gold may be left in the original solution. Treating the mixture with sodium cyanide in the presence of free oxygen dissolves the gold. The gold is removed from the solution by adsorbing (taking it up on the surface) to charcoal.
Bioleaching with fungi
Several species of fungi can be used for bioleaching. Fungi can be grown on many different strata, as with electronic scrap, catalytic converters, and fly ash from municipal waste incineration. Experiments have shown that two fungal strains (Aspergillus Niger, Penicillium simplicissimum) were able to mobilize Cu and Sn by 65%, and Al, Ni, Pb, and Zn by more than 95%.Aspergillus Niger can produce some organic acids such as citric acid. So it can be used for bioleaching sulfides .
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Bioleaching". A list of authors is available in Wikipedia.|