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Electrowinning, also called electroextraction, is the electrodeposition of metals from their ores that have been put in solution or liquefied. Electrorefining uses a similar process to remove impurities from a metal. Both processes use electroplating on a large scale and are important techniques for the economical and straightforward purification of non-ferrous metals.
In the case of electrowinning, a current is passed from an inert anode through a liquid leach solution containing the metal so that the metal is extracted as it is deposited in an electroplating process onto the cathode. In electrorefining, the anodes consist of unrefined impure metal, and as the current passes through the acidic electrolyte the anodes are corroded into the solution so that the electroplating process deposits refined pure metal onto the cathodes.
Additional recommended knowledge
It is the oldest industrial electrolytic process. Electrowinning was first demonstrated experimentally by von Leuchtenberg in 1747. Later, the English chemist Humphry Davy, obtained sodium metal in elemental form for the first time in 1807 by the electrolysis of molten sodium hydroxide. It was James Elkington, however who patented the commercial process in 1865 and opened the first successful plant in Pembrey, Wales in 1869.
The most common electrowon metals are lead, copper, gold, silver, zinc, aluminum, chromium, cobalt, manganese, and the rare-earth and alkali metals. For aluminum, this is the only practically used production process. Several industrially important active metals (which react strongly with water) are produced commercially by electrolysis of their pyrochemical molten salts. Experiments using electrorefining to process spent nuclear fuel have been carried out. Electrorefining could separate heavy metals such as plutonium, cesium, and strontium from the less-toxic bulk of uranium. Many electroextraction systems are also available to remove toxic (and sometimes valuable) metals from industrial waste streams.
Most metals occur in nature in oxidized form in their ores and thus must be reduced to their metallic forms. The ore is dissolved following some preprocessing in an aqueous electrolyte or in a molten salt and the resulting solution is electrolyzed. The metal is deposited on the cathode (either in solid or in liquid form), while the anodic reaction is usually oxygen evolution. Several metals are naturally present as metal sulfides; these include copper, lead, molybdenum, cadmium, nickel, silver, cobalt and zinc. In addition, gold and platinum group metals are associated with sulfidic base metal ores. Most metal sulfides or their salts, are electrically conductive and this allows electrochemical redox reactions to efficiently occur in the molten state or in aqueous solutions.
Some metals, including arsenic and nickel do not electrolyze out but remain in the electrolyte solution, these are then reduced by chemical reactions to refine the metal. Also after the process for the original target metal is complete, other metals which are reduced but not deposited at the cathode sink to the bottom of the electrolytic cell, where they form a substance referred to as anode sludge or anode slime. The metals in this sludge can be removed by standard pyrorefining methods.
Because metal deposition rates are related to available surface area, maintaining properly working cathodes is important. Two cathode types exist, flat-plate and reticulated cathodes, each with its own advantages. Flat-plate cathodes can be cleaned and reused, and plated metals recovered. Reticulated cathodes have a much higher deposition rate, compared to flat-plate cathodes. However, they are not reusable and must be sent off for recycling. Alternatively, starter cathodes of pre-refined metal can be used, becoming an integral part of the finished metal ready for rolling or further processing.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Electrowinning". A list of authors is available in Wikipedia.|