EP2978866A1 - Method and apparatus for recovering pgm and ferro-chrome from pgm bearing chromite ore - Google Patents
Method and apparatus for recovering pgm and ferro-chrome from pgm bearing chromite oreInfo
- Publication number
- EP2978866A1 EP2978866A1 EP14720990.2A EP14720990A EP2978866A1 EP 2978866 A1 EP2978866 A1 EP 2978866A1 EP 14720990 A EP14720990 A EP 14720990A EP 2978866 A1 EP2978866 A1 EP 2978866A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- slag
- furnace
- smelting furnace
- metal alloy
- concentrate
- 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.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims abstract description 40
- 229910000604 Ferrochrome Inorganic materials 0.000 title claims abstract description 25
- 238000003723 Smelting Methods 0.000 claims abstract description 55
- 239000002893 slag Substances 0.000 claims abstract description 52
- 239000012141 concentrate Substances 0.000 claims abstract description 30
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 29
- 229910001092 metal group alloy Inorganic materials 0.000 claims abstract description 28
- 239000011651 chromium Substances 0.000 claims abstract description 22
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 13
- 238000010438 heat treatment Methods 0.000 claims abstract description 13
- 229910052742 iron Inorganic materials 0.000 claims abstract description 13
- 229910052751 metal Inorganic materials 0.000 claims abstract description 11
- 239000002184 metal Substances 0.000 claims abstract description 11
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 6
- 239000000956 alloy Substances 0.000 claims abstract description 6
- 238000009854 hydrometallurgy Methods 0.000 claims abstract description 6
- 230000004907 flux Effects 0.000 claims description 8
- 239000003638 chemical reducing agent Substances 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 5
- -1 platinum group metals Chemical class 0.000 claims description 4
- 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
- 235000008504 concentrate Nutrition 0.000 claims 8
- 238000010079 rubber tapping Methods 0.000 claims 4
- 230000008569 process Effects 0.000 description 20
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 12
- 239000002994 raw material Substances 0.000 description 10
- 229910052697 platinum Inorganic materials 0.000 description 6
- 238000011084 recovery Methods 0.000 description 5
- 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
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 206010039509 Scab Diseases 0.000 description 2
- 241001062472 Stokellia anisodon Species 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-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
- 239000000463 material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 238000009853 pyrometallurgy Methods 0.000 description 2
- 229910000838 Al alloy 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
- 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
- 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
- 239000000571 coke Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper 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
- 238000004880 explosion Methods 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 229940096119 hydromet Drugs 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
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000008018 melting Effects 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
- 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
- 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
- 150000003568 thioethers Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
- 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
Definitions
- the invention relates to a method and an ap ⁇ paratus for recovering platinum group metals and fer- rochrome from PGM bearing chromite ore.
- Platinum group metals 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.
- 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 lo ⁇ cal producers cannot use all chromite-containing tail ⁇ ings 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 .
- US 6,699,302 Bl disclos ⁇ es 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 un ⁇ der 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 met ⁇ al alloy in a converter.
- 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 new method comprises preparing a concen ⁇ trate 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 fur ⁇ nace, where reduction of the oxides of iron and chro ⁇ mium contained in the slag takes place so that ferro ⁇ chrome is produced.
- the heating step additionally comprises roasting the concentrate to remove sulfur and/or volatiles con ⁇ tained in the concentrate.
- the slag properties are controlled with flux.
- the method comprises adding flux and/or reductant into the smelting furnace and/or into the slag furnace.
- the reducing conditions in the smelting furnace and/or in the slag furnace are controlled with the addition of reductant.
- the slag properties in the smelting furnace and/or in 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 pro- Derivatives or a combination of pyrometallurgical and hy ⁇ drometallurgical processes.
- 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 hydromet ⁇ allurgical process steps.
- molten metal alloy is tapped from the smelting furnace directly to an atomizer, after which the atom- ized 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 pro ⁇ ducing a ferrochrome alloy from the molten slag tapped from the DC smelting furnace.
- 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 pref ⁇ erably selected from a group comprising a fluidized bed reactor, a rotary kiln, a drying tower, or similar .
- the slag furnace can be an open bath alterna ⁇ tive current furnace, or similar.
- the apparatus further comprises a Peirce-Smith converter for removing iron from the molten metal alloy tapped from the smelting furnace.
- the apparatus further comprises an atomizer for atomizing the molten metal alloy tapped from the smelting furnace or from the converter.
- the present invention proposes using molten slag from a PGM smelter as a raw material in ferro ⁇ chrome production.
- 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 con- taining ore easier.
- the process also saves energy com ⁇ pared to current recovery processes.
- the ferrochrome containing slag fraction need not to be cooled and re ⁇ heated before introduction into 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 enclosed Figure 1 is a flow chart illus ⁇ tration of one embodiment of a process according to the present invention.
- 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 sep- arate chrome and iron from the base metals and PGMs.
- the concentrate is subjected to heat treat ⁇ ment 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 rota ⁇ ry 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 smelt- ing 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.
- carbonaceous reductant such as anthracite or coke
- some flux may be charged, if necessary.
- 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 be ⁇ low the lighter slag phase.
- most of the feed goes into the slag phase.
- all Cr and most of Fe, AI 2 O 3 , S 1O 2 , MgO and CaO of the feed go in ⁇ to 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.
- Liquid slag is tapped from the DC smelting furnace 14 to an AC slag furnace 16.
- Liquid metal al ⁇ loy is tapped from the bottom of the DC smelting fur- nace 14 to further refining steps in pyrometallurgical and/or hydrometallurgical processes.
- the slag furnace 16 is preferably an open bath alternative current furnace where electrodes are buried in a burden of lumpy materials comprised of molten slag received from DC smelting furnace. Carbo ⁇ naceous reductant and flux are charged to the AC fur ⁇ nace to control the reduction reactions and to opti ⁇ mize 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 AI 2 O 3 , MgO, CaO and S i0 2 - Metal alloy received from the slag furnace 16 contains Fe, Cr, some C and Si. All the rest of the feed is re ⁇ tained in the slag.
- Products received from the slag furnace 16 are ferrochrome metal and slag.
- 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, atom- ization 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.
- Benefits of the new process comprise simplic ⁇ ity of the preceding concentration process as there is no need to remove chromite at an early stage.
- FeCr and PGMs are produced at the same time, less concen ⁇ tration, 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 ex- plosion.
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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)
- Geochemistry & Mineralogy (AREA)
- General Engineering & Computer Science (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
In a method for recovering PGMs and ferrochrome from platinum group metals bearing chromite ore, a concentrate is prepared that contains most of PGMs and chromite of the ore and the concentrate is subjected to a heating step to dry and/or preheat the concentrate, after which the preheated concentrate is smelted under reducing conditions in a DC smelting furnace (14) to produce molten metal alloy containing the PGMs of the feed and molten slag containing the chromium of the feed. The molten slag is tapped from the smelting furnace (14) into an AC slag furnace (16), where iron and chromium are reduced to produce a ferrochrome alloy. PGMs are recovered from the metal alloy tapped from the smelting furnace (14) utilizing hydro-metallurgical processes.
Description
METHOD AND APPARATUS FOR RECOVERING PGM AND FERRO- CHROME FROM PGM BEARING CHROMITE ORE
FIELD OF THE INVENTION
The invention relates to a method and an ap¬ paratus for recovering platinum group metals and fer- rochrome from PGM bearing chromite ore.
BACKGROUND 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.
There are some challenges in using UG2 based raw material with current PGM recovery processes. One of the challenges is that traditional smelting furnac¬ es 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 furnac¬ es are susceptible to build-ups of high-melting chro¬ mite 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 smelt¬ ing 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 .
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 lo¬ cal producers cannot use all chromite-containing tail¬ ings 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 .
Attempts have been made to develop pyrometal- lurgical processes that tolerate higher chromite con¬ tents in the PGM concentrate. US 6,699,302 Bl disclos¬ es 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 un¬ der 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 met¬ al alloy in a converter.
Although the process of US 6, 699, 302 Bl 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. PURPOSE 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.
SUMMARY
The method according to the present invention is characterized by what is presented in claim 1.
The apparatus according to the present inven¬ tion is characterized by what is presented in claim 10.
The new method comprises preparing a concen¬ trate 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 fur¬ nace, where reduction of the oxides of iron and chro¬ mium contained in the slag takes place so that ferro¬ chrome is produced.
According to one embodiment of the invention the heating step additionally comprises roasting the concentrate to remove sulfur and/or volatiles con¬ tained in the concentrate.
According to one embodiment of the invention the 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.
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 slag properties in the smelting furnace and/or in 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 pro- cesses or a combination of pyrometallurgical and hy¬ drometallurgical 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 hydromet¬ allurgical 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 atom- ized 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 pro¬ ducing a ferrochrome alloy from the molten slag tapped 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 pref¬ erably selected from a group comprising a fluidized
bed reactor, a rotary kiln, a drying tower, or similar .
The slag furnace can be an open bath alterna¬ tive 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 another embodiment of the inven- tion 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 con- taining ore easier. The process also saves energy com¬ pared to current recovery processes. The ferrochrome containing slag fraction need not to be cooled and re¬ heated before introduction into 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.
BRIEF 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 in¬ vention .
The enclosed Figure 1 is a flow chart illus¬ tration 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 sep- arate chrome and iron from the base metals and PGMs.
The concentrate is subjected to heat treat¬ ment 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 rota¬ ry 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 smelt- ing 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.
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 be¬ low the lighter slag phase. However, most of the feed goes into the slag phase. For instance, all Cr and
most of Fe, AI2O3 , S 1O2 , MgO and CaO of the feed go in¬ to 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 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 im¬ proves reactions. A carbon monoxide atmosphere is cre¬ ated in the closed furnace. One more advantage of us- ing a DC smelting furnace is that it allows charging fine grinded material.
Liquid slag is tapped from the DC smelting furnace 14 to an AC slag furnace 16. Liquid metal al¬ loy is tapped from the bottom of the DC smelting fur- nace 14 to further refining steps in pyrometallurgical and/or hydrometallurgical processes.
The slag furnace 16 is preferably an open bath alternative current furnace where electrodes are buried in a burden of lumpy materials comprised of molten slag received from DC smelting furnace. Carbo¬ naceous reductant and flux are charged to the AC fur¬ nace to control the reduction reactions and to opti¬ mize 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 AI2O3 , MgO, CaO and S i02 - Metal alloy received from the slag furnace 16 contains Fe,
Cr, some C and Si. All the rest of the feed is re¬ tained 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, atom- ization 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.
Benefits of the new process comprise simplic¬ ity 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 concen¬ tration, 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 ex- plosion. There are fewer restrictions for raw materials and no limits for the Cr content of the feed. Nei¬ ther 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.
Claims
1. A method for recovering platinum group metals and ferrochrome from PGMs bearing chromite ore, comprising the steps of:
- 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,
- smelting the concentrate under reducing conditions in a DC smelting furnace (14) to produce molten metal alloy containing the PGMs of the feed and molten slag containing the chromium of the feed,
- tapping the molten slag from the smelting furnace (14) into an AC slag furnace (16),
- reducing the oxides of iron and chromium contained in the slag in the AC slag furnace (16) to produce ferrochrome alloy.
2. The method according to claim 1, wherein the heating step also comprises roasting the concen- trate to remove sulfur and/or volatiles contained in the concentrate.
3. The method according to claim 1 or 2, wherein the slag properties are controlled with flux.
4. The method according to any one of claims 1 to 3, comprising adding flux and/or reductant into the smelting furnace (14) and/or into the slag furnace (16) .
5. The method according to claim 4, wherein the reducing conditions in the smelting furnace (14) and/or in the slag furnace (16) are controlled with the addition of reductant.
6. The method according to any one of claims 3 to 5, wherein the slag properties in the smelting furnace (14) and/or in the slag furnace (16) are con- trolled with the addition of flux.
7. The method according to any one of claims 1 to 6, comprising tapping molten metal alloy from the
smelting furnace (14) and recovering PGMs from the metal alloy.
8. The method according to claim 7, compris¬ ing tapping molten metal alloy from the smelting fur- nace (14) to a Peirce-Smith converter (18) and/or subjecting the converted metal alloy to atomization and hydrometallurgical process steps.
9. The method according to claim 7, compris¬ ing tapping molten metal alloy from the smelting fur- nace (14) to an atomizer (20) and subjecting the atomized metal alloy to hydrometallurgical process steps.
10. An apparatus for recovering platinum group metals and ferrochrome from PGMs and chromite containing ore concentrate, comprising a DC smelting furnace (14) for producing a molten metal alloy containing the PGMs of the feed and a molten slag con¬ taining the chromium of the feed, and an AC slag fur¬ nace (16) for producing a ferrochrome alloy from the molten slag tapped from the DC smelting furnace (14) .
11. The apparatus according to claim 10, com¬ prising a heating unit (12) for drying and/or preheating the concentrate before it is fed to the smelting furnace (14), which heating unit (12) is selected from a group comprising a fluidized bed reactor, a rotary kiln, a drying tower, or similar.
12. The apparatus according to claim 10 or 11, wherein the slag furnace (14) is an open bath alternative current furnace, or similar.
13. The apparatus according to any one of claims 10 to 12, further comprising a Peirce-Smith converter (18) for removing iron from the molten metal alloy tapped from the smelting furnace (14) .
14. The apparatus according to any one of claims 10 to 13, further comprising an atomizer (20) for atomizing the molten metal alloy tapped from the smelting furnace (14) or from the converter (18) .
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| 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 |
| 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 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP2978866A1 true EP2978866A1 (en) | 2016-02-03 |
Family
ID=50630817
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP14720990.2A Withdrawn EP2978866A1 (en) | 2013-03-25 | 2014-03-25 | Method and apparatus for recovering pgm and ferro-chrome from pgm bearing chromite ore |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP2978866A1 (en) |
| CN (1) | CN105164285A (en) |
| BR (1) | BR112015024481A2 (en) |
| CA (1) | CA2907005C (en) |
| EA (1) | EA029428B1 (en) |
| FI (1) | FI125099B (en) |
| WO (1) | WO2014154945A1 (en) |
| ZA (1) | ZA201507020B (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10323302B2 (en) * | 2016-11-18 | 2019-06-18 | Heraeus Deutschland GmbH & Co. KG | Process for the production of a PGM-enriched alloy |
| US11772158B2 (en) | 2018-03-01 | 2023-10-03 | 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 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4295881A (en) * | 1979-04-23 | 1981-10-20 | Texasgulf Inc. | Process for extraction of platinum group metals from chromite-bearing ore |
| EP1157139B1 (en) * | 1999-02-26 | 2002-10-09 | Mintek | Treatment of metal sulphide concentrates by roasting and arc furnace smelt reduction |
| 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 |
-
2013
- 2013-03-25 FI FI20135284A patent/FI125099B/en not_active IP Right Cessation
-
2014
- 2014-03-25 CA CA2907005A patent/CA2907005C/en not_active Expired - Fee Related
- 2014-03-25 EA EA201591659A patent/EA029428B1/en not_active IP Right Cessation
- 2014-03-25 WO PCT/FI2014/050214 patent/WO2014154945A1/en not_active Ceased
- 2014-03-25 EP EP14720990.2A patent/EP2978866A1/en not_active Withdrawn
- 2014-03-25 BR BR112015024481A patent/BR112015024481A2/en not_active IP Right Cessation
- 2014-03-25 CN CN201480017592.6A patent/CN105164285A/en active Pending
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2015
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| Title |
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| See references of WO2014154945A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2907005C (en) | 2017-07-25 |
| EA201591659A1 (en) | 2016-04-29 |
| EA029428B1 (en) | 2018-03-30 |
| BR112015024481A2 (en) | 2017-07-18 |
| FI125099B (en) | 2015-05-29 |
| WO2014154945A1 (en) | 2014-10-02 |
| CN105164285A (en) | 2015-12-16 |
| FI20135284A7 (en) | 2014-09-26 |
| ZA201507020B (en) | 2017-01-25 |
| CA2907005A1 (en) | 2014-10-02 |
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