FI125099B - Process and apparatus for the recovery of platinum metals and ferrochrome from chromite ore containing platinum metals - Google Patents
Process and apparatus for the recovery of platinum metals and ferrochrome from chromite ore containing platinum metals Download PDFInfo
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- FI125099B FI125099B FI20135284A FI20135284A FI125099B FI 125099 B FI125099 B FI 125099B FI 20135284 A FI20135284 A FI 20135284A FI 20135284 A FI20135284 A FI 20135284A FI 125099 B FI125099 B FI 125099B
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- 238000000034 method Methods 0.000 title claims description 37
- 229910000604 Ferrochrome Inorganic materials 0.000 title claims description 25
- 229910052751 metal Inorganic materials 0.000 title claims description 18
- 239000002184 metal Substances 0.000 title claims description 18
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 title claims description 15
- -1 platinum metals Chemical class 0.000 title claims description 11
- 229910052697 platinum Inorganic materials 0.000 title description 8
- 238000011084 recovery Methods 0.000 title description 6
- 239000002893 slag Substances 0.000 claims description 46
- 238000003723 Smelting Methods 0.000 claims description 43
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 28
- 239000012141 concentrate Substances 0.000 claims description 26
- 239000011651 chromium Substances 0.000 claims description 21
- 229910001092 metal group alloy Inorganic materials 0.000 claims description 19
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 14
- 229910045601 alloy Inorganic materials 0.000 claims description 14
- 239000000956 alloy Substances 0.000 claims description 14
- 238000010438 heat treatment Methods 0.000 claims description 13
- 229910052742 iron Inorganic materials 0.000 claims description 13
- 229910052804 chromium Inorganic materials 0.000 claims description 12
- 238000002844 melting Methods 0.000 claims description 10
- 230000008018 melting Effects 0.000 claims description 9
- 230000004907 flux Effects 0.000 claims description 8
- 238000009854 hydrometallurgy Methods 0.000 claims description 7
- 239000003638 chemical reducing agent Substances 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 6
- 238000000889 atomisation Methods 0.000 claims description 3
- 239000003039 volatile agent Substances 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- UOUJSJZBMCDAEU-UHFFFAOYSA-N chromium(3+);oxygen(2-) Chemical class [O-2].[O-2].[O-2].[Cr+3].[Cr+3] UOUJSJZBMCDAEU-UHFFFAOYSA-N 0.000 claims 1
- 239000002994 raw material Substances 0.000 description 10
- 238000006722 reduction reaction Methods 0.000 description 5
- 239000010953 base metal Substances 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- 229910052976 metal sulfide Inorganic materials 0.000 description 3
- 238000009853 pyrometallurgy Methods 0.000 description 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 206010039509 Scab Diseases 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000002801 charged material Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 241001062472 Stokellia anisodon Species 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- RHZUVFJBSILHOK-UHFFFAOYSA-N anthracen-1-ylmethanolate Chemical compound C1=CC=C2C=C3C(C[O-])=CC=CC3=CC2=C1 RHZUVFJBSILHOK-UHFFFAOYSA-N 0.000 description 1
- 239000003830 anthracite Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000010891 electric arc Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910001338 liquidmetal Inorganic materials 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052566 spinel group Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
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- 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
- C22B11/00—Obtaining noble metals
- C22B11/02—Obtaining noble metals by dry processes
-
- 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
- C22B1/00—Preliminary treatment of ores or scrap
-
- 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
- C22B34/00—Obtaining refractory metals
- C22B34/30—Obtaining chromium, molybdenum or tungsten
- C22B34/32—Obtaining chromium
-
- 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
- C22B5/00—General methods of reducing to metals
- C22B5/02—Dry methods smelting of sulfides or formation of mattes
-
- 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
- C22B9/00—General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/04—Making ferrous alloys by melting
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27B—FURNACES, KILNS, OVENS OR RETORTS IN GENERAL; OPEN SINTERING OR LIKE APPARATUS
- F27B19/00—Combinations of different kinds of furnaces that are not all covered by any single one of main groups F27B1/00 - F27B17/00
- F27B19/04—Combinations of different kinds of furnaces that are not all covered by any single one of main groups F27B1/00 - F27B17/00 arranged for associated working
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/02—Making metallic powder or suspensions thereof using physical processes
- B22F9/06—Making metallic powder or suspensions thereof using physical processes starting from liquid material
- B22F9/08—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
- B22F9/082—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
-
- 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
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Manufacturing & Machinery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- General Engineering & Computer Science (AREA)
- Geochemistry & Mineralogy (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
METHOD AND APPARATUS FOR RECOVERING PGM AND FERRO-CHROME FROM PGM BEARING CHROMITE OREMETHOD AND APPARATUS FOR RECOVERING PGM AND FERRO-CHROME FROM PGM BEARING CHROMITE AIR
FIELD OF THE INVENTIONFIELD OF THE INVENTION
The invention relates to a method and an apparatus for recovering platinum group metals and fer-rochrome from PGM bearing chromite ore.The invention relates to a method and apparatus for recovering platinum group metals and ferrochrome from PGM bearing chromite in air.
BACKGROUND OF THE INVENTIONBACKGROUND OF THE INVENTION
Most of the world's known platinum reserves are located in South Africa, which produces most of the world's platinum. South Africa is also the world's largest single producer of ferrochrome. Platinum group metals, or PGMs, include platinum, rhodium, palladium, ruthenium, iridium, osmium. PGMs frequently occur together with chromites. The platinum industry in South Africa is increasingly moving from traditional Meren-sky reef to UG2 reef as a raw material. The UG2 reef contains most of the world's known PGM reserves, and it also has high chromite content.Most of the world's known Platinum reserves are located in South Africa, which produces most of the world's Platinum. South Africa is also the world's largest single producer of Ferrochrome. Platinum group metals, or PGMs, include Platinum, rhodium, palladium, ruthenium, iridium, osmium. PGMs Frequently occur together with chromites. The Platinum industry in South Africa is rapidly moving from the traditional Meren-sky Reef to UG2 Reef as a raw material. The UG2 Reef contains most of the world's known PGM reserves, and it also has high chromite content.
There are some challenges in using UG2 based raw material with current PGM recovery processes. One of the challenges is that traditional smelting furnaces cannot use a concentrate that contains over 2.5% Cr. If the chromium content is too high, Cr tends to create crust in the smelting furnace and the explosion risk is high. Traditional six-in-line smelting furnaces are susceptible to build-ups of high-melting chromite spinels if the Cr203 content of the feed is too high. Also the furnace control is very challenging. Furthermore, concentration process is rather complicated when the target is to separate the chromite from the PGMs. Traditionally, UG2 ore has been concentrated by removing chromite from the ore as far as possible to reach low chromite content in the PGM smelting furnace feed. It is very difficult to totally remove chromite from the concentrate by flotation. Chrome melts at temperatures above 1600°C, whereas PGM smelting furnaces operate at 1400-1500°C. The presence of chromium in the feed leads to lower furnace reduction efficiency and chromite can also damage the smelting furnace .There are some challenges in using UG2 based raw material with current PGM recovery processes. One of the challenges is that traditional Smelting Furnaces cannot use a Concentrate that contains over 2.5% Cr. If the chromium content is too high, Cr tends to create a crust in the smelting furnace and the risk of explosion is high. Traditional six-in-line Smelting Furnaces are susceptible to build-ups of high-melting chromite spinels if the Cr203 content of the feed is too high. Also the furnace control is very challenging. Furthermore, the concentration process is rather Complicated when the target is to separate the chromite from the PGMs. Traditionally, UG2 ore has been concentrated by removing chromite from the ore as far as possible to reach low chromite content in the PGM Smelting furnace feed. It is very difficult to completely remove chromite from the Concentrate by flotation. Chrome melts at temperatures above 1600 ° C, with PGM Smelting Furnaces operated at 1400-1500 ° C. The presence of chromium in the feed leads to lower furnace reduction efficiency and chromite can also damage the smelting furnace.
The UG2 concentration process used by the platinum industry in South Africa produces lots of chromite-containing tailings. Ferrochrome producers can use these tailings as raw material. South Africa suffers from shortage of electricity, which is why local producers cannot use all chromite-containing tailings of platinum industry but tailings are exported to China. The Chinese are building a lot of ferrochrome capacity now, which is worrying for the South African producers. One of the targets of the present invention is to provide a process that allows the South Africans to use their UG2 reserves more completely in their own country.The UG2 concentration process used by the Platinum industry in South Africa produces lots of chromite-containing tailings. Ferrochrome producers can use these tailings as raw material. South Africa suffers from a shortage of electricity which is why local producers cannot use all the chromite-containing tails of the Platinum industry but tails are exported to China. The Chinese are building a lot of Ferrochrome capacity now, which is worrying for South African producers. One of the targets of the present invention is to provide a process that allows South Africans to use their UG2 reserves more completely in their own country.
Attempts have been made to develop pyrometal-lurgical processes that tolerate higher chromite contents in the PGM concentrate. US 6,699,302 B1 discloses a method for processing metal sulfide concentrate that contains at least one metal selected from the group consisting of the PGMs, nickel, cobalt and zinc. The method comprises dead-roasting the metal sulfide concentrate, smelting the dead-roasted concentrate under reducing conditions in an electrically stabilized open-arc furnace, and collecting the metals from the smelting step in the form of an alloy or vapor. Chrome is an unwanted element and it is removed from the metal alloy in a converter.Attempts have been made to develop pyrometallurgical processes that tolerate higher chromite contents in the PGM Concentrate. US 6,699,302 B1 discloses a method for processing metal sulfide Concentrate that contains at least one metal selected from the group consisting of PGMs, nickel, cobalt and zinc. The method comprises dead-roasting the metal sulfide Concentrate, smelting the dead-roasting Concentrate under reducing conditions in an electrically stabilized open-arc furnace, and collecting the metals from the Smelting step in the form of an alloy or vapor. Chrome is an unwanted element and it is removed from the metal alloy in a Converter.
Although the process of US 6, 699,302 B1 can use raw materials with high chromium content, chrome is finally discarded from the process. Furthermore, the process is designed only for use with sulfide raw materials .Although the process of US 6, 699,302 B1 can use raw materials with high chromium content, chrome is finally discarded from the process. Furthermore, the process is designed only for use with sulfide raw materials.
The industry lacks a process that effectively combines the recovery of PGMs and ferrochrome from a PGM bearing chromite ore, such as UG2.The industry lacks a process that effectively combines the recovery of PGMs and Ferrochrome from a PGM bearing in chromite air, such as UG2.
PURPOSE OF THE INVENTIONPURPOSE OF THE INVENTION
The purpose of the present invention is to eliminate or at least reduce the problems of the prior art. A further purpose is to provide a new process for effective utilization of PGM bearing chromite ore.The purpose of the present invention is to eliminate or at least reduce the problems of prior art. A further purpose is to provide a new process for the effective utilization of PGM bearing in chromite air.
SUMMARYSUMMARY
The method according to the present invention is characterized by what is presented in claim 1.The method according to the present invention is characterized by what is presented in the claim 1.
The apparatus according to the present invention is characterized by what is presented in claim 10.The apparatus according to the present invention is characterized by what is claimed in the claim 10.
The new method comprises preparing a concentrate that contains most of the PGMs and chromite of the ore, subjecting the concentrate to a heating step to dry and/or preheat the concentrate, and smelting the concentrate under reducing conditions in a DC smelting furnace to produce molten metal alloy that contains the PGMs of the feed and molten slag that contains the chromium of the feed. The molten slag is tapped from the smelting furnace into an AC slag furnace, where reduction of the oxides of iron and chromium contained in the slag takes place so that ferrochrome is produced.The new method consists of preparing the Concentrate that contains most of the PGMs and chromite of the air, subjecting the Concentrate to a heating step to dry and / or preheat the Concentrate, and smelting the Concentrate under reducing conditions in a DC Smelting furnace to produce molten metal alloy that contains the PGMs of the feed and molten slag that contains the chromium of the feed. The molten slag is tapped from the smelting furnace into an AC slag furnace, where the reduction of the oxides of iron and chromium contained in the slag takes place so that Ferrochrome is produced.
According to one embodiment of the invention the heating step additionally comprises roasting the concentrate to remove sulfur and/or volatiles contained in the concentrate.According to one embodiment of the invention, the heating step additionally comprises roasting the Concentrate to remove the sulfur and / or volatiles contained in the Concentrate.
According to one embodiment of the invention the slag properties are controlled with flux.According to one embodiment of the invention, slag properties are controlled with flux.
Advantageously the method comprises adding flux and/or reductant into the smelting furnace and/or into the slag furnace.Advantageously the method consists of adding flux and / or reductant into the smelting furnace and / or into the slag furnace.
According to one embodiment of the invention the reducing conditions in the smelting furnace and/or in the slag furnace are controlled with the addition of reductant.According to one embodiment of the invention, the reducing conditions in the Smelting furnace and / or in the slag furnace are controlled with the addition of a reductant.
According to one embodiment of the invention the slag properties in the smelting furnace and/or in the slag furnace are controlled with the addition of flux.According to one embodiment of the invention, the slag properties in the Smelting furnace and / or the slag furnace are controlled with the addition of flux.
Advantageously molten metal alloy is tapped from the smelting furnace, after which PGMs are recovered from the metal alloy by hydrometallurgical processes or a combination of pyrometallurgical and hydrometallurgical processes.Advantageously, the metal alloy is tapped from the Smelting furnace, after which the PGMs are recovered from the metal alloy by hydrometallurgical processes or a combination of pyrometallurgical and hydrometallurgical processes.
According to one embodiment of the invention molten metal alloy from the smelting furnace is tapped to a Peirce-Smith converter, after which the converted metal alloy is subjected to atomization and hydrometallurgical process steps.According to one embodiment of the invention, molten metal alloy from the Smelting furnace is tapped to a Peirce-Smith Converter, after which the converted metal alloy is subjected to atomization and hydrometallurgical process steps.
According to another embodiment of the invention molten metal alloy is tapped from the smelting furnace directly to an atomizer, after which the atomized metal alloy is subjected to hydrometallurgical process steps.According to another embodiment of the invention, molten metal alloy is tapped from the smelting furnace directly to an atomizer, after which the atomized metal alloy is subjected to hydrometallurgical process steps.
The new apparatus comprises a DC smelting furnace for producing a molten metal alloy containing the PGMs of the feed and a molten slag containing the chromium of the feed, and an AC slag furnace for producing a ferrochrome alloy from the molten slag tapped from the DC smelting furnace.The new apparatus comprises a DC Smelting furnace for producing a molten metal alloy containing the PGMs of the feed and a molten slag containing the chromium of the feed and an AC slag furnace for producing a Ferrochrome alloy from the DC smelting furnace.
According to one embodiment of the invention the apparatus further comprises a heating unit for drying and/or preheating the concentrate before it is fed to the smelting furnace. The heating unit is preferably selected from a group comprising a fluidized bed reactor, a rotary kiln, a drying tower, or similar .According to one embodiment of the invention, the apparatus further comprises a heating unit for drying and / or preheating the Concentrate before it is fed to the Smelting furnace. The heating unit is preferably selected from the group consisting of a fluidized bed Reactor, a rotary kiln, a drying tower, or the like.
The slag furnace can be an open bath alternating current furnace, or similar.The slag furnace can be an open bath alternating current furnace, or similar.
According to one embodiment of the invention the apparatus further comprises a Peirce-Smith converter for removing iron from the molten metal alloy tapped from the smelting furnace.According to one embodiment of the invention, the apparatus further comprises a Peirce-Smith Converter for removing iron from the molten metal alloy tapped from the Smelting furnace.
According to another embodiment of the invention the apparatus further comprises an atomizer for atomizing the molten metal alloy tapped from the smelting furnace or from the converter.According to another embodiment of the invention, the apparatus further comprises an atomizer for atomizing the molten metal alloy tapped from the Smelting furnace or from the Converter.
Instead of using tailings from a PGM concentrator, the present invention proposes using molten slag from a PGM smelter as a raw material in ferro-chrome production. According to the new method both PGMs and ferrochrome are produced at the same time, which gives flexibility for the use of raw material and makes the concentration of PGM and chromite containing ore easier. The process also saves energy compared to current recovery processes. The ferrochrome containing slag fraction need not to be cooled and reheated before introduction into ferrochrome process.Instead of using tailings from a PGM concentrator, the present invention proposes using a molten slag from a PGM smelter as a raw material in Ferro-chrome production. According to the new method both PGMs and Ferrochrome are produced at the same time, which gives flexibility for the use of raw material and makes the concentration of PGM and chromite containing air easier. The process also saves energy compared to current recovery processes. The ferrochrome containing slag fraction need not be cooled and reheated before introduction into the ferrochrome process.
The present invention allows adjusting the Cr/Fe ratio in the ferrochrome by controlling how much iron is reduced in the smelting furnace. Typical use of pure UG2 ore results in Cr/Fe ratio of around 1.35, which means that the Cr content in the ferrochrome is below 50%. Higher Cr contents are preferred by the end users of ferrochrome, i.e. stainless steel industry.The present invention allows adjusting the Cr / Fe ratio in the Ferrochrome by controlling how much iron is reduced in the Smelting furnace. Typical use of pure UG2 in air results in a Cr / Fe ratio of about 1.35, which means that the Cr content in the Ferrochrome is below 50%. Higher Cr contents are preferred by end users of Ferrochrome, i.e. stainless steel industry.
BRIEF DESCRIPTION OF THE DRAWINGSBRIEF DESCRIPTION OF THE DRAWINGS
The accompanying drawing, which is included to provide further understanding of the invention and constitutes a part of this specification, illustrates an embodiment of the invention and together with the description helps to explain the principles of the invention .The accompanying drawing, which is included to provide further understanding of the invention, and is intended to provide a portion of this Specification, illustrates an explanation of the invention and together with the description helps to explain the principles of the invention.
The enclosed Figure 1 is a flow chart illustration of one embodiment of a process according to the present invention.The enclosed Figure 1 is a flow chart illustration of one embodiment of a process according to the present invention.
DETAILED DESCRIPTION OF AN EMBODIMENT PGM bearing chromite ore is fine grinded to liberate the PGM particles. The fine grinded ore is concentrated in a concentrator 10, where the target is to remove gangue while keeping iron, chromium, base metals and PGMs in the concentrate. The process is simpler than the concentration processes currently used in PGM recovery, because there is no need to separate chrome and iron from the base metals and PGMs.DETAILED DESCRIPTION OF AN EMBODIMENT PGM bearing chromite air is finely ground to liberate the PGM particles. The finely ground air is concentrated in a concentrator 10, where the target is to remove gangue while keeping iron, chromium, base metals and PGMs in the concentrate. The process is simpler than the concentration processes currently used in PGM recovery because there is no need to separate chromium and iron from the base metals and PGMs.
The concentrate is subjected to heat treatment in a heating unit 12, where the concentrate is dried, if necessary, and possibly preheated before it is fed to a smelting furnace 14. The heating unit 12 can be, for instance, a fluidized bed reactor, a rotary kiln, or a drying tower. If the raw material contains lots of sulfides and/or volatiles, roasting can be carried out in the heating unit 12 to oxidize the metal sulfides. CO gas generated in subsequent smelting and slag furnaces 14, 16 can be used as a heat source in the heating unit 12.The Concentrate is subjected to a heat treatment in a heating unit 12, where the Concentrate is dried, if necessary, and possibly preheated before it is fed to a Smelting furnace 14. The heating unit 12 can, for instance, be a fluidized bed reactor, a rotary kiln, or a drying tower. If the raw material contains lots of sulfides and / or volatiles, roasting can be carried out in the heating unit 12 to oxidize the metal sulfides. CO gas generated in subsequent Smelting and Slag Furnaces 14, 16 can be used as a heat source in the heating unit 12.
The preheated concentrate is charged as a feed into a DC smelting furnace 14. At the same time, carbonaceous reductant, such as anthracite or coke, is charged to the smelting furnace 14. Also some flux may be charged, if necessary.The preheated Concentrate is charged as a feed into a DC Smelting furnace 14. At the same time, carbonaceous reductant such as anthracite or Coke is charged to the Smelting furnace 14. Also some flux may be charged, if necessary.
In the DC smelting furnace 14 the concentrate is melted and the PGMs, base metals and part of the iron contained in the feed are reduced to elemental metal, which is separated as a molten metal alloy below the lighter slag phase. However, most of the feed goes into the slag phase. For instance, all Cr and most of Fe, AI2O3, Si02, MgO and CaO of the feed go into the slag phase. Reduction in the smelting furnace 14 is limited by controlling the amount of carbon charged to the furnace 14. The target is only to get the PGMs into metal phase together with just a part of the iron. Iron droplets capture the PGMs and other base metals, forming molten metal alloy. Ni and Cu can also be present in the molten metal alloy produced in the smelting furnace 14.In the DC Smelting Furnace 14 the Concentrate is melted and the PGMs, base metals and part of the iron contained in the feed are reduced to the elemental metal which is separated as a molten metal alloy below the lighter slag phase. However, most of the feed goes into the slag phase. For instance, all Cr and most of Fe, Al 2 O 3, SiO 2, MgO and CaO of the feed go into the slag phase. Reduction In Smelting Furnace 14 Is Limited By Controlling The Amount Of Carbon Charged In Furnace 14. Target Is Only To Get The PGMs Into The Metal Phase Together With Just A Part Of The Iron. Iron droplets Capture the PGMs and other base metals forming molten metal alloy. Ni and Cu can also be present in the molten metal alloy produced in the Smelting furnace 14.
In the direct current (DC) smelting furnace 14 the charged material is directly exposed to an electric arc, and the current between a cathode and an anode passes through the charged material. Energy is supplied by open plasma arc. The temperature in the smelting furnace 14 is relatively high, which is why reactions are quick. The plasma arc agitates the slag phase and creates strong currents, which further improves reactions. A carbon monoxide atmosphere is created in the closed furnace. One more advantage of using a DC smelting furnace is that it allows charging fine grinded material.In the direct current (DC) Smelting furnace 14 the charged material is directly exposed to the electric arc, and the current between the cathode and the anode passes through the charged material. Energy is supplied by open plasma arc. The temperature in the smelting furnace 14 is relatively high, which is why reactions are quick. The plasma arc agitates the slag phase and creates strong currents, which further improves the reactions. The carbon monoxide atmosphere is created in the closed furnace. One more advantage of using a DC Smelting Furnace is that it allows for Charging fine grinded material.
Liquid slag is tapped from the DC smelting furnace 14 to an AC slag furnace 16. Liquid metal alloy is tapped from the bottom of the DC smelting furnace 14 to further refining steps in pyrometallurgical and/or hydrometallurgical processes.Liquid slag is tapped from DC Smelting furnace 14 to an AC slag furnace 16. Liquid metal alloy is tapped from bottom to DC Smelting furnace 14 to further Refining steps in pyrometallurgical and / or hydrometallurgical processes.
The slag furnace 16 is preferably an open bath alternating current furnace where electrodes are buried in a burden of lumpy materials comprised of molten slag received from DC smelting furnace. Carbonaceous reductant and flux are charged to the AC furnace to control the reduction reactions and to optimize the amount and quality of slag. Typical ferro-chrome furnace operations comprise reduction of oxides of iron and chromium into metal phase. The resulting slag mainly contains A1203, MgO, CaO and Si02. Metal alloy received from the slag furnace 16 contains Fe,The slag furnace 16 is preferably an open bath alternating current furnace where electrodes are buried in the burden of lumpy materials comprised of molten slag received from DC Smelting furnace. Carbonaceous reductant and flux are charged to the AC furnace to control the reduction reactions and to optimize the amount and quality of the slag. Typical Ferro-chrome furnace operations include reduction of oxides of iron and chromium into metal phase. The resulting slag mainly contains A1203, MgO, CaO and SiO2. Metal alloy received from the slag furnace 16 contains Fe,
Cr, some C and Si. All the rest of the feed is retained in the slag. Products received from the slag furnace 16 are ferrochrome metal and slag. Typically, the temperature of the slag tapped from the AC slag furnace 16 is 1650-1750°C and the temperature of the ferrochrome tapped from the AC slag furnace 16 is 1550-1600°C. PGM rich metal alloy tapped from the smelting furnace 14 can either be directly passed to hydromet-allurgical treatment steps or it can be converted in a Peirce-Smith converter 18 before passing to hydromet-allurgical treatment. The purpose of converting is to remove iron and other impurities from the metal alloy. The recovery of PGMs can comprise, for instance, atomization in an atomizer 20 and leaching.Cr, some C and Si. All the rest of the feed is retained in the slag. Products received from the slag furnace 16 are Ferrochrome metal and slag. Typically, the temperature of the slag tapped from the AC slag furnace 16 is 1650-1750 ° C and the temperature of the ferrochrome tapped from the AC slag furnace 16 is 1550-1600 ° C. PGM rich metal alloy tapped from smelting furnace 14 can either be directly passed to hydrometallurgical treatment steps or it can be converted in a Peirce-smith converter 18 before passing to hydrometallurgical treatment. The purpose of Converting is to remove iron and other impurities from the metal alloy. The recovery of PGMs can comprise, for instance, atomization in an atomizer 20 and leaching.
The basic idea of the present innovation is to smelt the concentrate in a DC smelting furnace 14, where PGMs are reduced, and then to produce FeCr alloy from the slag of the DC smelting furnace in a separate AC slag furnace 16. This gives flexibility as regards the raw materials and simplifies the concentrating process 10.The basic idea of present innovation is to smelt the Concentrate in a DC Smelting Furnace 14, where PGMs are reduced, and then to produce FeCr alloy from the DC Smelting Furnace in a separate AC slag furnace 16. This gives flexibility as regards the raw materials and simplifies the concentrating process 10.
Benefits of the new process comprise simplicity of the preceding concentration process as there is no need to remove chromite at an early stage. As FeCr and PGMs are produced at the same time, less concentration, cooling and melting is needed and the process is more energy efficient. The safety of the process is improved as there is no risk of crust formation or explosion. There are fewer restrictions for raw materials and no limits for the Cr content of the feed. Neither Cr nor PGMs are lost in the process.Benefits of the new process include simplicity of the previous concentration process as there is no need to remove the chromite at an early stage. As FeCr and PGMs are produced at the same time, less concentration, cooling and melting are needed and the process is more energy efficient. The safety of the process is improved as there is no risk of crust formation or explosion. There are fewer restrictions on raw materials and no limits on the Cr content of the feed. Neither Cr nor PGMs are lost in the process.
It is obvious to a person skilled in the art that with the advancement of technology, the basic idea of the invention may be implemented in various ways. The invention and its embodiments are thus not limited to the examples described above; instead they may vary within the scope of the claims.It is obvious to a person skilled in the art that with the advancement of technology, the basic idea of invention can be implemented in various ways. The invention and its embodiments are thus not limited to the examples described above; instead they may vary within the scope of the claims.
Claims (14)
Priority Applications (8)
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FI20135284A FI125099B (en) | 2013-03-25 | 2013-03-25 | Process and apparatus for the recovery of platinum metals and ferrochrome from chromite ore containing platinum metals |
BR112015024481A BR112015024481A2 (en) | 2013-03-25 | 2014-03-25 | Method and apparatus for recovering pgm and ferro-chromium from pgm-bearing chromite ore |
CN201480017592.6A CN105164285A (en) | 2013-03-25 | 2014-03-25 | Method and apparatus for recovering PGM and ferro-chrome from PGM bearing chromite ore |
PCT/FI2014/050214 WO2014154945A1 (en) | 2013-03-25 | 2014-03-25 | Method and apparatus for recovering pgm and ferro-chrome from pgm bearing chromite ore |
EP14720990.2A EP2978866A1 (en) | 2013-03-25 | 2014-03-25 | Method and apparatus for recovering pgm and ferro-chrome from pgm bearing chromite ore |
EA201591659A EA029428B1 (en) | 2013-03-25 | 2014-03-25 | METHOD AND APPARATUS FOR RECOVERING PLATINUM GROUP METALS (PGMs) AND FERROCHROME FROM PGM BEARING CHROMITE ORE |
CA2907005A CA2907005C (en) | 2013-03-25 | 2014-03-25 | Method and apparatus for recovering pgm and ferro-chrome from pgm bearing chromite ore |
ZA2015/07020A ZA201507020B (en) | 2013-03-25 | 2015-09-21 | Method and apparatus for recovering pgm and ferro-chrome from pgm bearing chromite ore |
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FI20135284A FI125099B (en) | 2013-03-25 | 2013-03-25 | Process and apparatus for the recovery of platinum metals and ferrochrome from chromite ore containing platinum metals |
FI20135284 | 2013-03-25 |
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CN (1) | CN105164285A (en) |
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CA (1) | CA2907005C (en) |
EA (1) | EA029428B1 (en) |
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US10323302B2 (en) * | 2016-11-18 | 2019-06-18 | Heraeus Deutschland GmbH & Co. KG | Process for the production of a PGM-enriched alloy |
PE20220423A1 (en) | 2018-03-01 | 2022-03-29 | Aurum Integra Inc | METHOD FOR SELECTIVELY OXIDIZING METALS OF AN ALLOY |
US10435767B2 (en) | 2019-04-29 | 2019-10-08 | Techemet, LP | Low-flux converting process for PGM collector alloy |
US10472700B1 (en) | 2019-04-29 | 2019-11-12 | Techemet, LP | Converting process with partial pre-oxidation of PGM collector alloy |
CN112760549B (en) * | 2020-12-30 | 2022-02-22 | 邬海宇 | Process for smelting rare and noble metal ferroalloy in intermediate frequency furnace |
WO2023096525A1 (en) * | 2021-11-28 | 2023-06-01 | Татьяна Михайловна ПАРПОЛИТО | Furnace for producing ferrochromium alloys |
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US4295881A (en) * | 1979-04-23 | 1981-10-20 | Texasgulf Inc. | Process for extraction of platinum group metals from chromite-bearing ore |
ES2185575T3 (en) * | 1999-02-26 | 2003-05-01 | Mintek | TREATMENT OF METAL SULFIDE CONCENTRATES THROUGH TOSTATION AND FUSION REDUCTION IN AN ARC OVEN. |
DE102006052181A1 (en) * | 2006-11-02 | 2008-05-08 | Sms Demag Ag | A process for the continuous or discontinuous recovery of a metal or metals from a slag containing the metal or compound of the metal |
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CA2907005C (en) | 2017-07-25 |
ZA201507020B (en) | 2017-01-25 |
BR112015024481A2 (en) | 2017-07-18 |
EA029428B1 (en) | 2018-03-30 |
EP2978866A1 (en) | 2016-02-03 |
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CN105164285A (en) | 2015-12-16 |
CA2907005A1 (en) | 2014-10-02 |
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