AU2003232264A1 - Method for producing blister copper - Google Patents
Method for producing blister copper Download PDFInfo
- Publication number
- AU2003232264A1 AU2003232264A1 AU2003232264A AU2003232264A AU2003232264A1 AU 2003232264 A1 AU2003232264 A1 AU 2003232264A1 AU 2003232264 A AU2003232264 A AU 2003232264A AU 2003232264 A AU2003232264 A AU 2003232264A AU 2003232264 A1 AU2003232264 A1 AU 2003232264A1
- Authority
- AU
- Australia
- Prior art keywords
- slag
- copper
- smelting furnace
- reactor
- white metal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims description 55
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 239000002893 slag Substances 0.000 claims description 45
- 239000010949 copper Substances 0.000 claims description 44
- 229910052802 copper Inorganic materials 0.000 claims description 43
- 238000003723 Smelting Methods 0.000 claims description 42
- 238000000034 method Methods 0.000 claims description 36
- 230000001590 oxidative effect Effects 0.000 claims description 27
- 229910001361 White metal Inorganic materials 0.000 claims description 25
- 239000010969 white metal Substances 0.000 claims description 25
- 239000012141 concentrate Substances 0.000 claims description 18
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 16
- 229910052760 oxygen Inorganic materials 0.000 claims description 16
- 239000001301 oxygen Substances 0.000 claims description 16
- 239000000725 suspension Substances 0.000 claims description 14
- 239000000155 melt Substances 0.000 claims description 6
- 238000005422 blasting Methods 0.000 claims description 5
- 238000005188 flotation Methods 0.000 claims description 4
- 230000004907 flux Effects 0.000 claims description 3
- 238000002347 injection Methods 0.000 claims description 3
- 239000007924 injection Substances 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 18
- 229910052742 iron Inorganic materials 0.000 description 12
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 229910052717 sulfur Inorganic materials 0.000 description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000011593 sulfur Substances 0.000 description 6
- 238000010586 diagram Methods 0.000 description 4
- 229910004298 SiO 2 Inorganic materials 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- XOCUXOWLYLLJLV-UHFFFAOYSA-N [O].[S] Chemical compound [O].[S] XOCUXOWLYLLJLV-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- OMZSGWSJDCOLKM-UHFFFAOYSA-N copper(II) sulfide Chemical compound [S-2].[Cu+2] OMZSGWSJDCOLKM-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000002918 waste heat Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B15/00—Obtaining copper
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B15/00—Obtaining copper
- C22B15/0026—Pyrometallurgy
- C22B15/0028—Smelting or converting
- C22B15/003—Bath smelting or converting
- C22B15/0045—Bath smelting or converting in muffles, crucibles, or closed vessels
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B15/00—Obtaining copper
- C22B15/0026—Pyrometallurgy
- C22B15/0028—Smelting or converting
- C22B15/0047—Smelting or converting flash smelting or converting
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
WO 03/104504 PCT/FI03/00432 1 METHOD FOR PRODUCING BLISTER COPPER The invention relates to a method defined in claim 1 for producing blister copper. 5 In the flash smelting of copper, dried copper concentrate is fed into a flash smelting furnace together with oxygen-enriched air and silica sand. The energy required in the smelting process is obtained in the oxidation of sulfur and iron. The heat balance of the process is adjusted by means of an oxygen enrichment 10 of the process air, but sometimes oil or natural gas burners are also employed as sources for additional energy. Sulfur is oxidized into sulfur dioxide and iron is oxidized and slagged into iron silicate. The molten phases are separated from the gas in the settler -as the slag and matte are settled on the furnace bottom, so that the matte layer is placed lowest underneath. In flash smelting, like in 15 other copper smelting processes, the primary function of slag is to collect in a fluid form that can be tapped all iron oxides and silicatic and oxidic ingredients of the gangue created in the smelting process. Generally slag is cooled, crushed and flotated in order to recover the copper, or it is treated in reducing electric furnace processes. In the matte phase, which generally is further 20 treated in converting, there is obtained 50 - 70 percentages of copper. In the most generally applied Peirce-Smith converting, the iron contained by the matte phase is oxidized when blasting oxygen in the melt and forms, together with the added silica sand, fajalite slag that in the initial step of the converting process floats in the reactor on the surface of the white metal that is rich in copper. The 25 white metal contains 70 - 80 percentages of copper. When further blasting oxygen into the white metal, there is created blister copper, the copper content whereof is of the order 99 percentages. The slag still contains 5 - 10 percentages of copper, which is recovered by flotation and by feeding the slag concentrate that is rich in copper back into the flash smelting furnace or by 30 treating the slag in reducing conditions for example in an electric furnace.
WO 03/104504 PCT/FI03/00432 2 In principle it is economically sensible to directly produce blister copper, i.e. blister copper from sulfidic concentrate in one process step in a suspension reactor, with due respect to certain restrictions. The biggest problem here is that in said process, there is created a lot of slag, and also a large amount of 5 copper is collected in this slag. On the other hand, the treatment of slag in order to recover the copper contained therein causes extra expenses for the process. When the copper content in the concentrate is sufficiently high, typically at least 37 percentages by weight, it is economically profitable to produce blister copper in one process step. If the concentrate contains only slight amounts of iron or 10 other slag-forming components, in which case the amount of created slag is not so high, also the processing of a concentrate with a lower copper content is profitable. When producing blister copper, there is generally needed a two-step slag cleaning for the created slag in order to obtain a sufficiently high yield for the recovered copper. 15 According to the prior art, when operating within a given oxygen potential area, there appears so-called white metal in copper smelting, and in that case the copper content of the respective slag phase is essentially lower than in a case where the blister copper is in balance with the slag phase. In figure 1 (INSKO 20 261608 VIll, page 9), there is illustrated a sulfur-oxygen potential diagram for a Cu-Fe-S-O-SiO 2 system at the temperature 13000 C. In the figure there are seen contents of various phases occurring in the copper smelting process in different conditions. From the figure it can be seen that when white metal is present, the copper content of the respective slag is lower than with a slag 25 where the blister copper is in balance. From the publication PCT 00/09772, there is known a process for smelting copper concentrate in the presence of oxygen by continuously oxidizing the concentrate or the matte at a temperature of 1300 degrees or lower. According 30 to the process, the copper sulfide concentrate is smelted, the majority of the contained iron is removed as slag, and the majority of the sulfur turns into sulfur dioxide. The obtained product is white metal, matte or blister copper.
WO 03/104504 PCT/FI03/00432 3 The object of the present invention is to eliminate some of the drawbacks of the prior art. Another object of the invention is to prevent the creation of a slag with a high copper content in the production of blister copper. 5 The invention is characterized by what is set forth in the preamble of claim 1. Other embodiments of the invention are characterized by what is set forth in the other claims. The method according to the invention for producing blister copper has several 10 advantages. According to the method, concentrate, flux and oxygen-enriched air are together fed into a suspension smelting furnace, such as a flash smelting furnace, so that there are created at least two molten phases, a white metal phase and a slag phase, and the white metal is oxidized after the suspension smelting furnace at least in one oxidizing reactor. According to the 15 method, the operations in the suspension smelting furnace are advantageously carried out in conditions that provide for the creation of white metal, which means that the oxygen potential in the furnace is within the range 10-7 - 10-6 and the sulfur dioxide partial pressure is within the range 0,2-1. White metal is essentially composed of copper (70 - 80%) and sulfur. The white metal created 20 in the smelting does not substantially contain any slagging components. When operating in the above described conditions, there is advantageously created low-copper slag that is suited to be directly treated for recovering the copper, and there is not needed any separate primary reduction of slag for instance in an electric furnace. 25 The white metal is tapped out of the furnace either in continuous operation or in batches, in order to be oxidized in an oxidizing reactor, where the sulfur contained in the white metal is oxidized by using oxygen-enriched air, so that there are created sulfur dioxide and blister copper, but hardly any slag. 30 According to a preferred embodiment of the invention, the oxidizing reactor is arranged in a stationary fashion in connection with the suspension smelting furnace. According to another preferred embodiment of the invention, the WO 03/104504 PCT/FI03/00432 4 oxidizing reactor is connected to the suspension smelting furnace by a closed melt launder that provides for the transferring of the melt. When the oxidizing reactor is a closed reactor, the collection and recovery of the gases created in the process is more advantageously controlled. According to a preferred 5 embodiment of the invention, the oxidizing reactor is preferably a surface blasting reactor. According to another preferred embodiment, the oxidizing reactor is an injection reactor, by which also white metal in a solid state can advantageously be melted by injecting it into the melt together with oxidizing gas. The employed oxidizing reactor is advantageously for example of the type 10 Ausmelt, Isasmelt or Mitsubishi. Slag is tapped separately from the suspension smelting furnace and treated, according to a preferred embodiment of the invention, in an electric furnace in order to recover the copper content thereof. According to another preferred 15 embodiment of the invention, slag is after the suspension smelting furnace treated in flotation in order to recover the copper content. When applying the method according to the invention, there is advantageously not created any slag with a high copper content, and the unnecessary recirculation of copper and resulting copper losses are avoided. 20 The invention is explained in more detail below, with reference to the appended drawings. Figure 1 A sulfur-oxygen potential diagram for a Cu-Fe-S-0-SiO 2 system at the temperature of 13000 C 25 Figure 2a A process diagram of the process according to the invention. Figure 2b A process diagram of a process according to another preferred embodiment of the invention. Figure 2a illustrates the method according to the invention. Now concentrate 5, 30 flux 6 and oxygen-enriched air 7 are together fed into a flash smelting furnace WO 03/104504 PCT/FI03/00432 5 1, so that at the lower part 4 thereof there are created two molten phases, a white metal phase 11 and a slag phase 10. White metal 11 is oxidized after the flash smelting furnace in one oxidizing reactor 12, and there is created blister copper 15. In addition to white metal and slag, in the flash smelting furnace 5 there is created a small amount of blister copper, which also is conducted into the oxidizing reactor in 12. The process gases created in the flash smelting furnace 1 are conducted via the furnace uptake shaft 2 to a waste heat boiler 8, where the created dusts 9 are recirculated back into the flash smelting furnace, and the gases 17 are conducted to further treatment. The white metal 11 is 10 tapped out of the furnace 1 either in continuous operation or in batches into the oxidizing reactor 12, where the sulfur contained in the white metal is oxidized by oxygen-enriched air 16, so that there are created sulfur dioxide and blister copper 15, but not slag. According to a preferred embodiment of the invention illustrated in figure 2a, the oxidizing reactor 12 is arranged to be installed in 15 connection with the flash smelting furnace in a stationary fashion. In another embodiment of the invention, illustrated in figure 2b, the oxidizing reactor 12 is connected by means of a melt launder 13 directly to the flash smelting furnace. The slag 10 created in the flash smelting furnace 1 is conducted into slag treatment 14, alternatively either into an electric furnace or into flotation in order 20 to recover the copper content of the slag. According to a preferred embodiment of the invention, the oxidizing reactor is preferably a surface blasting or injection reactor, in which case also solid white metal can advantageously be melted by injecting it into the melt together with the oxidizing gas. The oxidizing reactor is preferably for example of the type Ausmelt, Isasmelt or Mitsubishi. 25 The invention is illustrated below by the following example. EXAMPLE By applying the method according to the invention, copper concentrate with a content of 30% Cu, 28% Fe, 30% S, 6% SiO 2 is smelted in a flash smelting 30 furnace at the rate of 163 tph (tph = tons/hour) together with silica sand, which is fed into the furnace at 21 tph.
WO 03/104504 PCT/FI03/00432 6 During the smelting process, into the flash smelting furnace there is blown air at the rate of 63,493 Nm 3 /h and oxygen at the rate of 21956 Nm 3 /h, so that the oxygen enrichment is 41 % and the oxygen coefficient is 171 Nm 3 02 when 5 calculated per one whole ton fed in. As a result of the oxidizing reactions, in the flash smelting furnace there is created molten white metal at 62,004 kg/h (content 79% Cu, 0.5% Fe) and slag at 109,702 kg/h (content 4% Cu, 44% Fe). In addition, there is created a small 10 amount of dust that is recirculated back into the smelting furnace. The slag is treated in a slag enrichment plant, so that the rate of created slag is 8,844 kg/h (content 46% Cu, 25% Fe), and said slag is then fed back into the flash smelting furnace together with the concentrate. 15 The created white metal is treated in an oxidizing reactor, into which there is fed technical oxygen at 4,328 Nm 3 /h and air at 18,979 Nm 3 /h. Now there is created blister copper at 49,274 kg/h (content 98% Cu, 0.04% Fe) and a small amount of slag (1 ton/h, content 50% Cu, 27% Fe). The slag is granulated and fed back 20 into the flash smelting furnace. In the example given above, the total quantity of copper recirculated back into the flash smelting furnace in slag concentrate and in the slag from the oxidizing reactor is 4,575 kg Cu, which corresponds to about 9% of the whole copper 25 quantity contained in the concentrate. If the concentrate were smelted directly into blister, the slag quantity would be about 130 t/h, and it would contain even more than 50% of the total copper quantity contained in the concentrate. For a man skilled in the art, it is obvious that the various embodiments of the invention are not restricted to the examples illustrated above, but may vary 30 within the appended claims.
Claims (8)
1. A method for producing blister copper, according to which method copper concentrate (5), flux (6) and oxygen-enriched air (7) are fed 5 together into a suspension smelting furnace (1), such as a flash smelting furnace, so that there are created at least two molten phases, such as white metal (11) and slag (10), characterized in that white metal is oxidized after the suspension smelting furnace in at least one oxidizing reactor (12). 10
2. A method according to claim 1, characterized in that oxidizing reactor (12) is arranged to be installed in connection with the suspension smelting furnace (1) in a stationary fashion. 15
3. A method according to claim 1, characterized in that the oxidizing reactor (12) is connected to the suspension smelting furnace (1) by a melt launder (13).
4. A method according to claim 1 - 3, characterized in that the oxidizing 20 reactor (12) is a surface blasting reactor.
5. A method according to claim 1 - 3, characterized in that the oxidizing reactor (12) is an injection reactor. 25
6. A method according to claim 5, characterized in that into the oxidizing reactor (12), there also is injected solid white metal.
7. A method according to claim 1, characterized in that the slag (10) is after the suspension smelting furnace (1) treated in an electric fqunace in 30 order to recover the copper content thereof. WO 03/104504 PCT/FI03/00432 8
8. A method according to claim 1, characterized in that the slag (10) is after the suspension smelting furnace (1) treated in flotation in order to recover the copper content thereof.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI20021114 | 2002-06-11 | ||
| FI20021114A FI116069B (en) | 2002-06-11 | 2002-06-11 | Procedure for making raw cups |
| PCT/FI2003/000432 WO2003104504A1 (en) | 2002-06-11 | 2003-06-02 | Method for producing blister copper |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2003232264A1 true AU2003232264A1 (en) | 2003-12-22 |
Family
ID=8564117
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2003232264A Abandoned AU2003232264A1 (en) | 2002-06-11 | 2003-06-02 | Method for producing blister copper |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US20050199095A1 (en) |
| EP (1) | EP1511868A1 (en) |
| JP (1) | JP2005536629A (en) |
| KR (1) | KR20050007600A (en) |
| CN (1) | CN100385024C (en) |
| AR (1) | AR040256A1 (en) |
| AU (1) | AU2003232264A1 (en) |
| BR (1) | BR0311758A (en) |
| CA (1) | CA2488398A1 (en) |
| EA (1) | EA007445B1 (en) |
| FI (1) | FI116069B (en) |
| MX (1) | MXPA04012084A (en) |
| PE (1) | PE20040137A1 (en) |
| PL (1) | PL372533A1 (en) |
| RS (1) | RS107704A (en) |
| WO (1) | WO2003104504A1 (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FI117769B (en) * | 2004-01-15 | 2007-02-15 | Outokumpu Technology Oyj | Feeding system in a suspension melting furnace |
| DE102005008684B4 (en) * | 2004-03-05 | 2008-10-09 | Merck Patent Gmbh | Use of liquid crystal displays and methods for their utilization |
| CA2565643C (en) * | 2006-06-28 | 2011-08-02 | Nippon Mining & Metals Co., Ltd. | Operation method of copper smelting |
| FI120157B (en) * | 2007-12-17 | 2009-07-15 | Outotec Oyj | Process for processing copper copper |
| JP4908456B2 (en) | 2008-06-02 | 2012-04-04 | パンパシフィック・カッパー株式会社 | Copper smelting method |
| CN102605191B (en) | 2012-04-16 | 2013-12-25 | 阳谷祥光铜业有限公司 | Method for directly producing row copper by copper concentrate |
| US9725784B2 (en) | 2012-06-21 | 2017-08-08 | Lawrence F. McHugh | Production of copper via looping oxidation process |
| CN102876902A (en) * | 2012-10-18 | 2013-01-16 | 铜陵有色金属集团股份有限公司金冠铜业分公司 | Method for composite smelting of copper concentrate flash-molten bath and outokumpu flash furnace |
| FI125793B (en) | 2014-05-14 | 2016-02-15 | Outotec Finland Oy | Procedure for converting materials containing copper |
| JP6466869B2 (en) * | 2016-02-29 | 2019-02-06 | パンパシフィック・カッパー株式会社 | Operation method of copper smelting furnace |
| BE1025772B1 (en) * | 2017-12-14 | 2019-07-08 | Metallo Belgium | Improvement in copper / tin / lead production |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5230259B2 (en) * | 1974-03-30 | 1977-08-06 | ||
| FI52358C (en) * | 1974-11-11 | 1977-08-10 | Outokumpu Oy | A method of continuously producing raw copper in one step from impure sulfide copper concentrate or ore. |
| DE2941225A1 (en) * | 1979-10-11 | 1981-04-23 | Klöckner-Humboldt-Deutz AG, 5000 Köln | METHOD AND DEVICE FOR PYROMETALLURGIC PRODUCTION OF COPPER |
| US4416690A (en) * | 1981-06-01 | 1983-11-22 | Kennecott Corporation | Solid matte-oxygen converting process |
| US4470845A (en) * | 1983-01-05 | 1984-09-11 | Newmont Mining Corporation | Continuous process for copper smelting and converting in a single furnace by oxygen injection |
| FI67727C (en) * | 1983-06-15 | 1985-05-10 | Outokumpu Oy | FOERFARANDE FOER ATT TILLVERKA RAOKOPPAR |
| CA1323495C (en) * | 1988-04-29 | 1993-10-26 | Marc Reist | Process and apparatus for converting of solid high-grade copper matte |
| US5194213A (en) * | 1991-07-29 | 1993-03-16 | Inco Limited | Copper smelting system |
| CN1067113C (en) * | 1998-08-08 | 2001-06-13 | 徐有生 | Pollution-free fire smelting method for Cu-Ni sulphide mine |
| TR200201715T2 (en) * | 2000-01-04 | 2002-10-21 | Outokumpu Oyj | Method for the production of blister copper in suspension reactor |
-
2002
- 2002-06-11 FI FI20021114A patent/FI116069B/en active IP Right Grant
-
2003
- 2003-06-02 CA CA002488398A patent/CA2488398A1/en not_active Abandoned
- 2003-06-02 CN CNB038135205A patent/CN100385024C/en not_active Expired - Fee Related
- 2003-06-02 PE PE2003000540A patent/PE20040137A1/en not_active Application Discontinuation
- 2003-06-02 KR KR10-2004-7020015A patent/KR20050007600A/en not_active Withdrawn
- 2003-06-02 AU AU2003232264A patent/AU2003232264A1/en not_active Abandoned
- 2003-06-02 WO PCT/FI2003/000432 patent/WO2003104504A1/en not_active Ceased
- 2003-06-02 RS YUP-1077/04A patent/RS107704A/en unknown
- 2003-06-02 PL PL03372533A patent/PL372533A1/en not_active Application Discontinuation
- 2003-06-02 BR BR0311758-8A patent/BR0311758A/en not_active IP Right Cessation
- 2003-06-02 EA EA200401402A patent/EA007445B1/en unknown
- 2003-06-02 EP EP03757080A patent/EP1511868A1/en not_active Withdrawn
- 2003-06-02 MX MXPA04012084A patent/MXPA04012084A/en unknown
- 2003-06-02 JP JP2004511562A patent/JP2005536629A/en not_active Abandoned
- 2003-06-02 US US10/517,506 patent/US20050199095A1/en not_active Abandoned
- 2003-06-10 AR ARP030102064A patent/AR040256A1/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| WO2003104504A1 (en) | 2003-12-18 |
| AR040256A1 (en) | 2005-03-23 |
| EA200401402A1 (en) | 2005-06-30 |
| CN1659293A (en) | 2005-08-24 |
| RS107704A (en) | 2007-04-10 |
| KR20050007600A (en) | 2005-01-19 |
| BR0311758A (en) | 2005-03-08 |
| FI20021114A0 (en) | 2002-06-11 |
| CN100385024C (en) | 2008-04-30 |
| PL372533A1 (en) | 2005-07-25 |
| EA007445B1 (en) | 2006-10-27 |
| US20050199095A1 (en) | 2005-09-15 |
| FI116069B (en) | 2005-09-15 |
| PE20040137A1 (en) | 2004-05-05 |
| EP1511868A1 (en) | 2005-03-09 |
| CA2488398A1 (en) | 2003-12-18 |
| JP2005536629A (en) | 2005-12-02 |
| MXPA04012084A (en) | 2005-03-07 |
| FI20021114L (en) | 2003-12-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Bellemans et al. | Metal losses in pyrometallurgical operations-A review | |
| KR102613147B1 (en) | Improved process for the production of crude solder | |
| CA1245460A (en) | Oxidizing process for sulfidic copper material | |
| US6270554B1 (en) | Continuous nickel matte converter for production of low iron containing nickel-rich matte with improved cobalt recovery | |
| US20050199095A1 (en) | Method for producing blister copper | |
| KR100929520B1 (en) | Production method of crude or high quality mat | |
| US4415356A (en) | Process for autogenous oxygen smelting of sulfide materials containing base metals | |
| KR100658405B1 (en) | Method for the production of blister copper in suspension reactor | |
| US4487628A (en) | Selective reduction of heavy metals | |
| EP3143169B1 (en) | A method of converting copper containing material | |
| CA2098521C (en) | Method for producing high-grade nickel matte and metallized sulfide matte | |
| JPS6156258A (en) | Continuous dry refining method and apparatus of copper/lead mat | |
| CA1112456A (en) | Method of manufacturing crude iron from sulphidic iron-containing material | |
| EP0427699B1 (en) | Method and apparatus for treating zinc concentrates | |
| ZA200409879B (en) | Method for producing blister copper. | |
| JPS58161734A (en) | Production of metal lead from sulfide rich ore | |
| WO1997020958A1 (en) | Recovery of cobalt from slag | |
| JPH0152454B2 (en) | ||
| Mackey et al. | Advances in pyrometallurgy—1983 | |
| KR20250004214A (en) | Method for treating zinc concentrate | |
| US4457779A (en) | Oxidizing flux for simultaneous smelting/converting sulfides of high gangue content | |
| BG64652B1 (en) | Method for the production of blister copper in a suspension reactor | |
| GB2088413A (en) | Process for Autogenous Oxygen Smelting of Sulphide Materials Containing Base Metals |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK1 | Application lapsed section 142(2)(a) - no request for examination in relevant period |