Smelting of copper concentrates produces matte and slag. Copper matte is converted into blister copper in Peirce-Smith, Hoboken discontinuous converters or by using continuous converting processes such as the Kennecott-Outokumpu or Mitsubishi processes. Blister copper is directed to fire refining process prior electro-refining.
The fire refining process is a classical batch process consisting of four stages: charging, oxidation and impurities slagging, reduction and anode casting. After oxidation and slagging, copper contains from 5000 to 10000 ppm of oxygen. Oxygen must be reduced to 800 or 1,200 ppm prior to the anodes casting.
Continuous conversion processes, as the Mitsubishi and Kennecott-Outokumpu processes, and the classical conversion processes in Peirce-Smith or Hoboken converters use to work in the blister over-oxidation mode due to their tendency to work with higher grade matte. Thus, blister copper may contain from 4,000 to 6,000 ppm of oxygen. If content of impurities, especially arsenic and antimony, is low enough for not requiring addition of fluxes, blister copper needs only to be degasified, and is ready for reduction.
Copper is reduced with fossil reducers or ammonia. The most commonly used reducers are oil and natural gas. Oil or natural gas is injected with air into the bath of molten copper through tuyères. Copper reduction faces significant limitations in the process rate and efficiency of reducer utilization. Reducer efficiency is below 50%. Injection of liquid or gaseous reducer into the copper produces black fumes in off-gas due to the thermal decomposition of hydrocarbons. Partial carbon utilization in reduction of oxygen from copper causes the presence of carbon particles in the reduction gases, which are partly burnt if the burner flame is oxidizing. Carbon particles are transferred to the furnace off-gas, creating black fumes, which are emitted through a chimney to the atmosphere.
L. Klein suggested the use of a gaseous reducer instead of wood, “Gaseous Reduction of Oxygen-Containing Copper”, J. of Metals, Col 13, No. 8, August 1961, 545-547, U.S. Pat. No. 2,989,397 June 1961. The study showed that injection of natural gas with air is a better solution that the injection of natural gas only into the liquid copper. The method for deoxidizing copper with reformed natural gas and the related apparatus were patented by Phelps Dodge Corporation in USA and Canada. C. Kuzell, M. Fowler, S. Davis and L. Klein: “Apparatus for Reforming Gases”; U.S. Pat. No. 3,071,454, January 1963; “Gaseous Reduction of Oxygen-Containing Copper”, CA 668,598, August 1963.
R. Beck, C. Andersen and M. Messner patented the process for deoxidizing copper with natural gas-air mixtures, “Process for Deoxidizing Copper with Natural Gas-Air Mixtures”, U.S. Pat. No. 3,619,177, November 1971.
The company Anaconda patented a process for deoxidizing copper in a vascular furnace through the injection of the mixture of natural gas or oil and water vapor; W. Foard and R. Lear, “Refining Copper”, U.S. Pat. No. 3,529,956, September 1970.
J. Henderson and W. Johnston patented for ASARCO the method of copper reduction in a vascular furnace by injection of natural gas through tuyères “Gas poling of copper”, U.S. Pat. No. 3,623,863, November 1971.
G. Mckerrow and D. Panell reviewed in the paper “Gaseous deoxidization of Anode Copper at the Noranda Smelter”, Canadian Metallurgical Quarterly, Vol. 11, No. 4, 1972, 629-633, the evolution of methods of copper deoxidization in Noranda smelter using natural gas injected through tuyères in a vascular furnace. J. Oudiz made a general review of the copper reduction processes (“Poling processes for copper refining”, J. of Metals, Vol 25, December 1973, 35-38).
C. Toro and V. Paredes “Sustitución parcial del petróleo diesel por Enap-6 como agente reductor en el proceso de obtención de cobre anódico en la fundición Potrerillos” (“Partial substitution of diesel oil with Enap-6 as reducing agent in the process for obtaining anodic copper at the Potrerillos Smelter”), 34th IIMCh Annual Convention, November 1983, Rancagua, developed and demonstrated in an industrial scale the possibilities of the use of heavy oil (ENAP-6), which has a higher sulphur content and costs less, in copper reduction.
The only continuous fire reduction process patented is that of Wuth et al, W. Wuth, G. Melcher, H. Weigel, Klockner Humbolt Deutz AG, “Process for Continuously Refining Contamined Copper in the Molten Phase”, ZA 7603039, Apr. 27, 1977; Klockner Humbolt Deutz AG, “Method of Continuous Refining of Impure Copper in the Liquid Phase” GB 1525786, Sep. 20, 1978; H. Weigel, G. Melcher, W. Wuth (Klockner Humbolt Deutz AG), “Method for Continuous Refining of Contamined Copper in the Molten Phase” US 127408, Nov. 28, 1978, was developed at a small pilot scale at the beginning of the 70s, and never found an industrial application. The process is based on the continuous flow of copper through two reverberating furnaces. In the first furnace copper is oxidized by air blown through vertical nozzles and in the second furnace copper is reduced with reducing oil or gas injected through vertical nozzles.
The new continuous copper reduction process in a bed covered with charcoal patented by Warczok et al, A. Warczok, G. Riveros, T. Utigard, T. Martin, G. Wastavino, H. Schwarze, D. Smith, J. Sanhueza, A. Balocchi, L. Gonzalez, S. Wanner, A. Fielzweiser, P. Gray, “Meted de Refinancing a Fuego Continua de Cobre” (“Copper Continuous Fire Refining Method”), Chilean patent application CL 2269-04, September 2004, has been developed at a pilot industrial scale. Reduction of oxidized copper takes place in a reaction with a bed covered with charcoal.
This invention refers to a hydrometallurgical method for continuous reduction of oxidized copper through combustion gases, which use the gravitational flow of liquid copper through a reactor with covered bed.
Sources of oxidized copper are:
Blister copper of continuous or batch conversion may be reduced if content of impurities is acceptable for electro-refining, and only needs to be deoxidized.
This invention has the following advantages as compared to the traditional copper reduction methods:
Figure No. 1 show a schematic diagram that illustrates the oxidized copper intense, continuous reduction principle in a reactor with covered bed.
Thus, this invention corresponds to a continuous copper reduction method consisting of the following stages:
[CnHm]fuel+(n+m/4)/2[O2]air=>n[CO]gas+m/4[H2]gas+m/4[H2O]gas
[Cu2O]copper+CO=>2[Cu]copper+CO2
[Cu2O]copper+H2=>2[Cu]copper+H2O
The oxidized copper dispersed on the surface of the ceramic covered bed flows downward in the form of veins or drops that are in contact with the hot gas that flows countercurrent, and contains hydrogen and carbon monoxide. The very high liquid copper surface area and volume ratio results in a high reduction ratio. Natural gas, propane and oil injected with a sub-stechiometric quantity of air generate hot reducing gases, which in turn deoxidize the copper. Temperature of copper and its content of oxygen may be precisely controlled through the air and fuel flow.
Continuous copper refining in a small smelter with a production capacity of 40,000 tons/year, which corresponds to a continuous copper flow of 5 tons/hour.
Blister copper flows from the retaining furnace to the oxidizing furnaces defined by the method defined in the patent description by authors Warczok et al., A. Warczok, G. Riveros, T. Utigard, T. Martin, G. Wastavino, H. Schwarze, D. Smith, J. Sanhueza, A. Balocchi, L. González, S. Wanner, A. Fielzweiser, P. Grau, “Método de Refinación a Fuego Continua de Cobre” (“Copper Continuous Fire Refining Method”), Chilean patent application CL 2269-04, September 2004. Oxidized copper temperature is maintained in a range from 1,190° C. to 1,210° C. and content of oxygen in a range from 7,500 to 8,500 ppm. The oxidized copper flows through a 4 meters long canal directly to the reduction furnace. The round reduction furnace has a diameter of 1.2 meters and a height of 1.8 meters, and is filled with chrome-magnesite grains (of a diameter of 30 to 40 mm). The mixture of air (80 to 100 Nm3/h) and natural gas (20 to 30 Nm3/h) is injected through the tuyère over the chrome-magnesite covered bed through three tuyères. The natural gas plays a fuel-reducer role. The additional air (100 Nm3/h) is injected through the tuyère over the covered bed for post-combustion of gases. The temperature of the refined copper is maintained within a range of 1,190° C. and 1,200° C., and content of oxygen within a range of 800 to 1,200 ppm. Copper is continuously evacuated to a pot and transported to the retaining furnace.
The Kenneth-Outokumpu continuous conversion process produces blister copper with an oxygen level of 5,000 ppm in a smelter with a production capacity of 160,000 tons/year. Copper production corresponds to a continuous flow of 20 tons/h of copper. Content of impurities is acceptable for electro-refining. Blister copper must only be deoxidized. Oxidized copper flows through a 12 meters long anal directly to the reduction furnace. The reduction furnace has a diameter of 2.2 meters and a height of 3.5 meter, and is filled with chrome-magnesite grains (of a diameter of 30 to 40 mm). The mixture of air (350 Nm3/h) and natural gas (80 Nm3/h) is injected through three tuyères over the covered bed.
The additional air (400 Nm3/h) is blown through a tuyère over the covered bed for post-combustion of gases. The temperature of the refined copper is maintained within a range of 1,190° C. and 1,200° C., and content of oxygen within a range of 800 to 1,200 ppm. Copper is continuously bled or evacuated through a siphon-type block, and flows directly to the anodes casting wheel. Use of two casting wheels ensures continuous operation.
Number | Date | Country | Kind |
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3701-2007 | Dec 2007 | CL | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/IB2008/003545 | 12/18/2008 | WO | 00 | 10/11/2011 |