The present invention relates to a method and equipment, whereby matte with a high non-ferrous metal content and disposable slag are produced simultaneously in a suspension smelting furnace from non-ferrous sulphide concentrate. According to the invention, a carbonaceous reducing agent is charged to the lower furnace of a suspension smelting furnace via tuyeres to a section of the furnace with a reduced cross-sectional area.
It is characteristic in suspension smelting that the final phase equilibrium between the slag and matte only arises during the slag reactions taking place in the lower furnace. In other words, the potentially imbalanced over-and under-oxidized compounds formed in the reaction shaft still react with each other in the slag phase, particularly in the primary discharge point of the shaft suspension under the reaction shaft, so that the massive slag and matte phase are almost in the composition defined by their thermodynamic composition. In addition to the previously mentioned equilibrium-determining copper already dissolved in the slag, copper-rich matte, undissoluble to the slag, remains in the slag as a mechanical suspension, which does not manage to settle in a realistic time.
It is known before that slag with a low copper content can be produced in a suspension smelting furnace such as flash smelting furnace, when fixed coke or some other carbonaceous substance is used in the reduction of slag and the copper oxidule dissolving therein and especially magnetite which increases the viscosity of the slag and slows down the separation of molten matte particles contained in the slag by settling.
In U.S. Pat. No. 5,662,370 a method is described, in which it is essential that the carbon content of the carbonaceous material to be charged to the reaction shaft is at least 80%, that at least 65% of the material particles are under 100 μm and at least 25% between 44-100 μm. Particle size is defined precisely, because, according to said patent, the reduction of magnetite with unburnt coke occurs under two mechanisms and particle size is of decisive significance with regard to said mechanisms. If the rough coke powder size is about 100 μm or greater, the particle size of the unburnt part is also great and for this reason coke remains floating on the slag surface and reactions are slow. When particle size is reduced, the powder coke enters the slag and thus comes into direct contact with the magnetite to be reduced, which accelerates the reaction rate.
In Japanese patent application 58-221241 a method is described, in which coke breeze or coke breeze together with pulverized coal are charged into the reaction shaft of a flash smelting furnace through a concentrate burner. The coke is fed into the furnace so that the entire surface of the melt in the lower furnace is evenly covered with the unburnt powder coke. According to the application, the degree of reduction of magnetite decreases when the grain size is ultra-fine, so grain size used is preferably from 44 μm to 1 mm.
In JP patent 90-24898 there is described a method, in which pulverized coke or coal with particle size of under 40 mm is fed into the flash smelting furnace to replace the oil used as an extra fuel and maintain the desired temperature in the furnace.
JP patent application 9-316562 applies to the same method as the previously mentioned U.S. Pat. No. 5,662,370. The difference from the method of the US patent is that carbonaceous material is fed to the lower part of the reaction shaft of the flash smelting furnace, to prevent said carbonaceous material from burning before it reaches the slag and the magnetite to be reduced contained therein. The particle size of the carbonaceous material is essentially the same as the distribution described in the US patent.
A weakness of the previously described methods is that the reduction area is the same where slag material and non-ferrous metallic matte come to when they settle from the reaction shaft and separate from the gas phase in the lower furnace. However, in a suspension smelting furnace, fine grained material such as copper matte particles does also drift with the gas phase to the back of the furnace and uptake. When these smallest particles separate from the gas flow in the back of the furnace and settle to the surface of the slag phase, their settling in the slag phase is very slow due to just the small particle size. Because slag mainly is tapped from the back or side of the furnace, these particles do not manage to settle through the slag phase. Instead, they drift together with the slag to be tapped out of the furnace and add to the copper content of slag.
Another weakness in some of the previously described methods is the small particle size of the coke, in that these coke particles do not settle at all from the gas phase but continue with the gas phase to the uptake and from there on to a waste-heat boiler as a reducing agent. In the boiler the coke particles react and generate unnecessary energy in the wrong place, which may even limit total process capacity as the waste-heat boiler capacity diminishes.
One clear disadvantage of the previously described methods is that the reducing impact of the coke and then the minimum content of the slag are directed in an uncontrolled manner throughout the lower furnace area including particularly the area underneath of the reaction shaft, which has an essential impact on the non-ferrous metal content of the matte produced. In other words, the massive coke layer which forms on the surface of the slag phase renders the process uncontrollable. Now in the method developed, it is possible to reduce the slag further without essentially affecting the metal content of the massive non-ferrous metallic matte such as copper or nickel matte produced in the process without disturbing the slag reactions in the shaft suspension.
In a method according to the present invention developed for non-ferrous metal production in a suspension-smelting furnace, the slag forming in a lower furnace is injected with pulverized coke or other carbonaceous reducing agent via tuyeres into an area, which does not disturb either the natural slag reactions of the suspension which discharges from a reaction shaft and the generation of matte. So the tuyere injection is either done in the area between the reaction shaft and the uptake, under the uptake or in a separate extension of the lower furnace located after the uptake. The difficulty of a tuyere injection in metallurgical processes is that its impact area is short depth-wise and in a conventional suspension smelting furnace effective impact would not be possible due to the width of the furnace. For this reason, according to the present invention, a throttle area with an essentially reduced cross-sectional area is incorporated into the furnace, where the tuyeres are located. It is essential that the slag-tapping hole is located so that the total amount of melt has to flow through this tuyere area, thereby reducing the slag. The reduction area precedes a settling area, where the matte and metal particles separated from the slag by reduction can settle. The essential features of the invention will become apparent in the attached patent claims.
It is also known before that the viscosity of slag in slag reduction decreases with lowering of ferric iron content which increases viscosity, wherein the settling of particles separated in reduction occurs more rapidly than in a normal suspension smelting. In addition, in the method of the present invention the flows caused by the injection achieve desired turbulence in the melt, so the small particles therein which settle slowly have an improved chance of joining each other or straight to the matte phase, which in turn makes the cleansing of slag from metal more effective.
The invention is described further in the attached diagrams, where:
The alternative presented in
Number | Date | Country | Kind |
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991110 | May 1999 | FI | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCTFI00/00396 | 5/4/2000 | WO | 00 | 6/3/2002 |
Publishing Document | Publishing Date | Country | Kind |
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WO0070103 | 11/23/2000 | WO | A |
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4470845 | Yannopoulos | Sep 1984 | A |
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4857104 | Victorovich et al. | Aug 1989 | A |
5458672 | Ding | Oct 1995 | A |
5662730 | Akagi et al. | Sep 1997 | A |
Number | Date | Country |
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58-221241 | Dec 1983 | JP |
59-050132 | Mar 1994 | JP |
09-316562 | Dec 1997 | JP |