MXPA05005997A - Method for treating slag. - Google Patents
Method for treating slag.Info
- Publication number
- MXPA05005997A MXPA05005997A MXPA05005997A MXPA05005997A MXPA05005997A MX PA05005997 A MXPA05005997 A MX PA05005997A MX PA05005997 A MXPA05005997 A MX PA05005997A MX PA05005997 A MXPA05005997 A MX PA05005997A MX PA05005997 A MXPA05005997 A MX PA05005997A
- Authority
- MX
- Mexico
- Prior art keywords
- copper
- slag
- leaching
- vesicular
- created
- Prior art date
Links
- 239000002893 slag Substances 0.000 title claims abstract description 47
- 238000000034 method Methods 0.000 title claims abstract description 35
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 63
- 239000010949 copper Substances 0.000 claims abstract description 63
- 229910052802 copper Inorganic materials 0.000 claims abstract description 62
- 239000012141 concentrate Substances 0.000 claims abstract description 16
- 238000003723 Smelting Methods 0.000 claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 claims abstract description 12
- 239000000725 suspension Substances 0.000 claims abstract description 10
- 238000002386 leaching Methods 0.000 claims description 16
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 15
- 238000001556 precipitation Methods 0.000 claims description 9
- 238000011084 recovery Methods 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 3
- 241000894006 Bacteria Species 0.000 claims description 2
- 238000005868 electrolysis reaction Methods 0.000 claims description 2
- 238000000622 liquid--liquid extraction Methods 0.000 claims description 2
- 238000000638 solvent extraction Methods 0.000 claims description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 12
- 238000002474 experimental method Methods 0.000 description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 229910052742 iron Inorganic materials 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000005266 casting Methods 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- MBMLMWLHJBBADN-UHFFFAOYSA-N Ferrous sulfide Chemical compound [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- BWFPGXWASODCHM-UHFFFAOYSA-N copper monosulfide Chemical compound [Cu]=S BWFPGXWASODCHM-UHFFFAOYSA-N 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 239000012535 impurity 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
- 239000006028 limestone Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052569 sulfide mineral Inorganic materials 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 238000001238 wet grinding Methods 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
- C22B7/00—Working up raw materials other than ores, e.g. scrap, to produce non-ferrous metals and compounds thereof; Methods of a general interest or applied to the winning of more than two metals
- C22B7/04—Working-up slag
-
- 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
- C22B15/0054—Slag, slime, speiss, or dross treating
-
- 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
-
- 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
- C22B7/00—Working up raw materials other than ores, e.g. scrap, to produce non-ferrous metals and compounds thereof; Methods of a general interest or applied to the winning of more than two metals
- C22B7/006—Wet processes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Environmental & Geological Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Electrolytic Production Of Metals (AREA)
- Processing Of Solid Wastes (AREA)
- Extraction Or Liquid Replacement (AREA)
- Water Treatment By Electricity Or Magnetism (AREA)
Abstract
The invention relates to a method for treating slag created in the production of blister copper processed directly from concentrate in a suspension smelting furnace, such as a flash smelting furnace, in order to recover the copper, so that at least part of the slag is leached in at least one step.
Description
METHOD FOR SCREEN TREATMENT
Field of the Invention The invention relates to a method that is defined in the preamble of claim 1 for the treatment of slag created in the production of vesicular copper.
Background of the Invention The production of vesicular copper from sulfur concentrates directly in a single stage in a suspension reactor, such as an ultra-fast melting furnace, is economically sensitive, with certain boundary conditions. Among the most notable problems that exist in the direct production of vesicular copper is the scorification of copper and the large amounts of slag that are created. In order to ensure a sufficient recovery of the copper, the amount of copper found in the slag must be recovered in relation to the slag cleaning. Apart from the amount of slag, another problem involves the large amounts of heat created in the combustion of sulfur concentrates. In that case, a low oxygen enrichment in the process air is applied, which means that the heating of the nitrogen contained in the process air balances the heat economy. However, this produces a large amount of process gases, which again results in a large furnace space and above all in large gas processing units. In the case where the copper content of the concentrate is sufficiently high, typically at least 37% Cu, vesicular copper production is economically possible directly in one stage. The thermal value of the concentrate is generally lower, the higher the copper content of the concentrate. With a high copper content, the iron sulfide mineral part is low. When the concentrate described above is processed, a sufficiently high oxygen enrichment can be used and, as a result, the gas quantities can be maintained at a moderate level. Also a concentrate with a low copper content is adequate in the production of vesicular copper, if it has a low iron content, in which case the amount of slag created is not noticeably large. From the Finnish patent application No. 982818 a method for the production of vesicular copper is known, in which method, in addition to the concentrate, molten and cooled copper matte are conducted to a casting reactor. Now a smaller amount of slag has been created in proportion to the amount of vesicular copper produced than with the traditional method. Now copper losses in slag have also been reduced. The slag created is further processed either in a single stage cleaning process or preferably in a two stage cleaning process. A two-stage slag cleaning method includes either two electric furnaces or an electric furnace and a slag concentrate plant. In the electric furnace the slag is reduced by coke, so that the precious metals bound in the slag phase are reduced and separated as a distinctive copper phase below the slag layer. In the event that the slags are processed in a slag concentration plant, the slag concentrate can be fed back to the smelting reactor. The vesicular copper is driven to be refined in an anode furnace. If the slag is processed in a single stage in an electric furnace, so that the amount of copper in the slag is economically insignificant, the iron content in the vesicle is still so high that a separate treatment for the vesicular is often required in a converter. One method is the pre-treatment of electric furnace, where vesicular copper created is processed together with bulk vesicular in an anode furnace, but there is still a lot of copper in the slag that for economic reasons must be recovered by technical means of concentration.
OBJECTIVES OF THE INVENTION The objective of the invention is to introduce a new method for the treatment of slag created in the production of vesicular copper that is produced directly from a concentrate. A particular objective of the invention is to achieve a more effective and more advantageous way, with respect to the global economy, to recover copper slagging in the production of vesicular copper.
The invention is characterized by what is established in the characterizing part of claim 1. Other embodiments of the invention are characterized by what is established in the rest of the claims.
BRIEF DESCRIPTION OF THE DRAWINGS The invention is described in more detail below and with reference to the accompanying drawings, in which Figure 1 is a diagram of a process according to the invention.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The method according to the invention has many advantages. According to the method, the copper contained in the slag created in the production of vesicular copper produced directly from the concentrate is advantageously recovered. The method of the invention simplifies the recovery of the copper and, in addition, the method makes possible an improved control of the impurities. The recovery of the copper contained in hydrometallurgical slag reduces the energy consumption compared to the reduction of the electric furnace. In addition, gas and dust emissions are reduced compared to pyrometallurgical recovery. Figure 1 illustrates a method according to the invention for slag processing, that is, vesicle slag, created in the production of vesicular copper that is produced in a suspension smelting furnace, such as an ultra-fast smelting furnace, with in order to recover the copper, in which case at least a part of the slag is leached in at least one stage. The concentrate of copper, flux and air enriched with oxygen are fed to the smelter 1 in a smelting furnace in suspension, such as an ultra-fast casting furnace. The dry concentrate particles react rapidly in a hot suspension with air enriched with oxygen. The energy that is released in the reactions is used in the process. Part of the sulfur is oxidized in sulfur dioxide, and the iron is oxidized in iron oxides, thus creating slag with the flux. The reaction products are sedimented in the lower part of the smelting furnace in suspension, creating two separate and molten phases: vesicular copper and vesicular slag. The gases created in the process are conducted additionally, to be processed in a way that is known. The vesicular copper created in the smelting furnace in suspension is conducted to an anode oven treatment 2, where it is refined in a manner that is already known and is emptied into copper anodes. The vesicle slag created in the smelter 1 is poured out of the smelting furnace in suspension through provided circulation channels, such as tundishes, and is further conducted to be treated in order to recover the copper contained in the smelter. vesicular slag. First the vesicle slag is transferred to a granulation and grinding stage 3. The granulated vesicular slag is milled for example in a wet milling operation at a given grain size in order to obtain a larger reaction surface. In the leaching step 4, the metals contained in the vesicle slag are leached. According to the example given below, the leaching 4 is carried out under oxidation conditions with sulfuric acid, so that copper sulfate is created. The amount of sulfuric acid added is advantageously 500-900 grams per kilogram of slag. The leaching can also be carried out by means of an ammonia solution, a doric solution or as a leaching of bacteria. After the leaching stage, from the solution containing metal sulphates, the copper is separated in the copper precipitation stage 5. In the copper precipitation stage, from the solution containing metal sulphates, the copper is precipitated for example by hydroxide precipitation or sulfur precipitation. In precipitation of hydroxide, the copper is precipitated by limestone and the precipitate created and containing the copper is conducted back to the stage of smelting 1. In the precipitation of sulfur copper is precipitated by hydrogen sulfide and the precipitate created and which contains copper is conducted back to casting stage 1. Copper can also be recovered by liquid-liquid extraction and electrolysis as cathode copper.
Example In order to verify the method, sulfuric acid solution experiments were carried out in a two-liter acid-proof reactor with a lid. The reactor was provided with four flow deflector plates, a reflux condenser and an agitator. A continuous pH meter, a temperature regulator and oxygen bubbling under the agitator blades had also been connected to the reactor. A heat plate was used for heating. At the beginning of the experiment, the slag (200 grams) was leached in water, the amount of water being a little less than one liter. In all the experiments the total volume of water and sulfuric acid added was exactly one liter. The temperature of the solution was 90 ° C. The amount of sulfuric acid (H2SO4) that was added in the experiment was 806 g / 1000 g of slag. The leaching period in all the experiments was 6 hours, and mechanical agitation experiments (approximately 770 revolutions / minute) as well as oxygen (0.50 liters per minute) were applied to the experiments. Strong sulfuric acid (95% by weight content) was added gradually and at the same time the temperature was adjusted to 90 ° C. The reaction time measurement was started when all the acid had been delivered. Slurry samples were taken when 0, 2, 4 and 6 hours had passed since the beginning of the experiment. In the filtrate and precipitate of the sample, the content of copper (Cu) and iron (Fe) was analyzed. Originally the leached slag contained 32.5% Cu and 23% Fe. The analyzes and yields of the leaching obtained on the bases already provided are presented in the following table:
The weight of the final precipitate was 77.4 grams and the copper content was 3.1%, which means that the total copper produced in the solution was 96.3%. The experiment was repeated under similar conditions for the slag that was, instead of cooled slowly, granulated by water directly from the molten state, so that the product obtained was finely divided with the corresponding composition. The total leaching yield obtained for copper under similar conditions was 95.8%, which is of the same order as with slow cooling slag, when the accuracy of the analysis is taken into account. From the solution, the copper was precipitated selectively by adjusting the acidity, so that the iron was precipitated in the first stage and the copper in the second stage, and in this way the unwanted iron could be separated from the copper. It is obvious to a person skilled in the art that the various preferred embodiments of the invention are not restricted to the foregoing examples only, but may vary within the scope of the appended claims.
Claims (10)
- Claims 1. A method for the recovery of copper from slag created in the production of vesicular copper processed directly from concentrate in a smelting furnace in suspension, such as an ultra-fast smelting furnace, characterized in that at least part of the slag it is leached in at least one stage to dissolve copper from the slag, the dissolved copper is precipitated and the precipitated copper is returned to the smelting process.
- 2. A method according to claim 1, characterized in that the slag is granulated and ground prior to leaching.
- 3. A method according to claim 1 or 2, characterized in that the leaching is carried out with sulfuric acid.
- 4. A method according to claim 1 or 2, characterized in that the leaching is carried out with an ammoniacal solution.
- 5. A method according to claim 1 or 2, characterized in that the leaching is carried out with a doric solution.
- 6. A method according to claim 1 or 2, characterized in that the leaching is carried out as a solution of bacteria.
- A method according to any of the preceding claims, characterized in that after leaching, the copper is recovered by hydroxide precipitation.
- 8. A method according to claim 1-6, characterized in that after leaching, the copper is recovered by sulfide precipitation.
- 9. A method according to claim 1-6, characterized in that after leaching, the copper is recovered in a liquid-liquid extraction and electrolysis as cathode copper. A method according to claim 7 or 8, characterized in that the copper-containing slag created in the precipitation is conducted back into the smelting furnace in suspension.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FI20022150A FI115638B (en) | 2002-12-05 | 2002-12-05 | Procedure for treating slag |
PCT/FI2003/000898 WO2004050925A1 (en) | 2002-12-05 | 2003-11-24 | Method for treating slag |
Publications (1)
Publication Number | Publication Date |
---|---|
MXPA05005997A true MXPA05005997A (en) | 2005-08-18 |
Family
ID=8565039
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MXPA05005997A MXPA05005997A (en) | 2002-12-05 | 2003-11-24 | Method for treating slag. |
Country Status (14)
Country | Link |
---|---|
US (1) | US20060037435A1 (en) |
EP (1) | EP1579017A1 (en) |
JP (1) | JP2006509103A (en) |
KR (1) | KR20050085402A (en) |
CN (1) | CN1720342A (en) |
AR (1) | AR042301A1 (en) |
AU (1) | AU2003283455A1 (en) |
BR (1) | BR0317061A (en) |
EA (1) | EA200500756A1 (en) |
FI (1) | FI115638B (en) |
MX (1) | MXPA05005997A (en) |
PE (1) | PE20040630A1 (en) |
PL (1) | PL376932A1 (en) |
WO (1) | WO2004050925A1 (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FI116686B (en) | 2003-07-17 | 2006-01-31 | Outokumpu Oy | Method for melting copper ligands |
EP2053137A1 (en) * | 2007-10-19 | 2009-04-29 | Paul Wurth S.A. | Recovery of waste containing copper and other valuable metals |
FI120157B (en) * | 2007-12-17 | 2009-07-15 | Outotec Oyj | A process for refining copper concentrate |
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 |
KR101389430B1 (en) * | 2012-08-23 | 2014-04-25 | 엘에스니꼬동제련 주식회사 | The recovery method of valuble metals included in converter slag at copper smelter |
KR101502592B1 (en) * | 2013-04-12 | 2015-03-16 | 주식회사 삼삼 | slag treatment method for extracting silic and magnesia |
JP6363035B2 (en) * | 2015-02-27 | 2018-07-25 | 独立行政法人国立高等専門学校機構 | Copper slag treatment method |
RU2614293C2 (en) * | 2015-06-04 | 2017-03-24 | Общество с ограниченной ответственностью "Институт Гипроникель" | Method of low-autogenous raw material processing in flash smelting furnaces |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2693405A (en) * | 1952-06-20 | 1954-11-02 | Sherritt Gordon Mines Ltd | Method of separating copper values from and ammoniacal solution |
US3224873A (en) * | 1963-02-25 | 1965-12-21 | Gen Mills Inc | Liquid-liquid recovery of copper values using alpha-hydroxy oximes |
US3632308A (en) * | 1969-12-05 | 1972-01-04 | Universal Oil Prod Co | Recovery of copper values from slag |
US3928551A (en) * | 1970-07-27 | 1975-12-23 | American Cyanamid Co | Leaching polyelectrolyte fluidized solids |
DE2348005A1 (en) * | 1972-09-25 | 1974-07-25 | Albright & Wilson | PROCESS FOR THE EXTRACTION OF COPPER AND / OR ZINC FROM WASTE |
US4034063A (en) * | 1974-03-22 | 1977-07-05 | Industrial Resources, Inc. | Process for control of SOx emissions from copper smelter operations |
US4152142A (en) * | 1977-02-28 | 1979-05-01 | Kennecott Copper Corporation | Recovery of copper values from iron-containing ore materials as mined and smelted |
US4484730A (en) * | 1982-09-30 | 1984-11-27 | Iso "Metalurgkomplekt" | Device for leaching copper from slags |
NO156724C (en) * | 1983-07-08 | 1987-11-11 | Elkem As | PROCEDURE FOR EXPLOITING THE COPPER CONTENT IN SULPHIDIC ORE AND CONCENTRATES. |
US5616168A (en) * | 1994-02-28 | 1997-04-01 | Kennecott Utah Copper Corporation | Hydrometallurgical processing of impurity streams generated during the pyrometallurgy of copper |
MXPA02006652A (en) * | 2000-01-04 | 2002-09-30 | Outokumpu Oy | Method for the production of blister copper in suspension reactor. |
CA2363969C (en) * | 2001-11-26 | 2009-01-13 | Walter Curlook | Process for the recovery of residual metal values from smelter waste slags, and from converter slags |
FI114808B (en) * | 2002-05-03 | 2004-12-31 | Outokumpu Oy | Process for the processing of precious metal |
-
2002
- 2002-12-05 FI FI20022150A patent/FI115638B/en not_active IP Right Cessation
-
2003
- 2003-11-24 CN CNA2003801049585A patent/CN1720342A/en active Pending
- 2003-11-24 KR KR1020057010244A patent/KR20050085402A/en not_active Application Discontinuation
- 2003-11-24 WO PCT/FI2003/000898 patent/WO2004050925A1/en not_active Application Discontinuation
- 2003-11-24 PL PL37693203A patent/PL376932A1/en not_active Application Discontinuation
- 2003-11-24 EP EP20030775423 patent/EP1579017A1/en not_active Withdrawn
- 2003-11-24 US US10/536,631 patent/US20060037435A1/en not_active Abandoned
- 2003-11-24 BR BR0317061A patent/BR0317061A/en not_active IP Right Cessation
- 2003-11-24 MX MXPA05005997A patent/MXPA05005997A/en unknown
- 2003-11-24 AU AU2003283455A patent/AU2003283455A1/en not_active Abandoned
- 2003-11-24 EA EA200500756A patent/EA200500756A1/en unknown
- 2003-11-24 JP JP2004556365A patent/JP2006509103A/en not_active Abandoned
- 2003-12-02 PE PE2003001224A patent/PE20040630A1/en not_active Application Discontinuation
- 2003-12-04 AR ARP030104479 patent/AR042301A1/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
PE20040630A1 (en) | 2004-11-11 |
US20060037435A1 (en) | 2006-02-23 |
AU2003283455A1 (en) | 2004-06-23 |
FI20022150A0 (en) | 2002-12-05 |
JP2006509103A (en) | 2006-03-16 |
AR042301A1 (en) | 2005-06-15 |
EP1579017A1 (en) | 2005-09-28 |
CN1720342A (en) | 2006-01-11 |
FI20022150A (en) | 2004-06-06 |
KR20050085402A (en) | 2005-08-29 |
EA200500756A1 (en) | 2005-12-29 |
BR0317061A (en) | 2005-10-25 |
WO2004050925A1 (en) | 2004-06-17 |
FI115638B (en) | 2005-06-15 |
PL376932A1 (en) | 2006-01-09 |
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