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WELCOME TO EXTRACTIVE
METALLURGY PRESENTATION ON:
MANGANESE
MANGANESE DEPOSITS – South Africa
EXTRACTIVE METALLURGY:
MANGANESE
PYROLUSITE MANGANESE METAL
Soumya Sobhan Dash
Department of Metallurgy and Material Engineering
National Institute of Technology,
ROURKELA, INDIA
PRESENTED BY:
INTRODUCTION
 MANGANESE is an Important Metal (Mn – 25) with many Metal Alloys , in particular Stainless Steel.
 The major Mineral Ore for Mn is Pyrolusite – MnO2( Manganese Dioxide).
 J G Gahn (1774) was First to isolate Manganese metal by Reducing MnO2 with Carbon.
 Manganese is the 12th most abundant Earth element.
 Manganese Ores in nature are Pyrolusite(MnO2), Braunite, Psilomelane, Rhodocrosite etc.
 South Africa produces 80% of World Manganese output.
 Manganese Nodules on the Ocean floor are yet to be Harvested commercially profitably .
 Ferro-Manganese Alloys are produced with MnO2 ore, iron ore &Carbon smelting in a Blast
Furnace/ Electric Arc Furnace.
 Iron free Manganese Alloys are produced by Leaching MnO2 Ores with H2SO4 soln. & subsequent
Electrowinning process .
 Heap Leaching of MnO2 Ores with Natural Gas at 850 ̊C & in presence of CO results in formation of
MnO which is easily leached with H2SO4 & Fe(II) Iron to produce Iron Hydroxide & Elemental
Manganese, to be Electrowinned into Manganese Metal.
 Manganese is essential to Steel production by virtue of it’s Sulfur fixing, Deoxidizing &Alloying
properties.
 Steel containing 8-15% of Manganese results in High Tensile strength
 Aluminium –Manganese Alloy (0.8-1.5% Mn) results in Galvanic Corrosion free Alloy used in
Beverage cans.
 Organo-metallic Manganese Tricarbonyl compound added to Unleaded Gasoline boosts Octane
rating of Fuel.
History:
Metallic manganese was first isolated in 1774 by Johan Gottlieb Gahn, a Swedish
mineralogist who reduced Pyrolusite, a manganese dioxide ore, with carbon. In
1856 Robert Forester Mushet, a British steelmaker, used manganese to improve the
ability of steel produced by the Bessemer process to withstand rolling and forging at
elevated temperatures. A tough wear-resistant steel containing approximately 12
percent manganese was developed in Sheffield, England, by Robert Abbott Hadfield in
1882. Ferromanganese was first smelted commercially in a blast furnace in 1875;
electric-furnace production began in 1890. Pure manganese was not available
commercially until 1941, following work on electrolysis conducted in the 1930s under
S.M. Shelton at the U.S. Bureau of Mines. By the early 21st century, manganese
production had expanded to several locations throughout the world, and Australia,
South Africa, China, Gabon, and Brazil became the largest producers.
Johan Gottlieb Gahn
WORLDMANGANESE SCENARIO
WORLD MANGANESE RESERVES & PRODUCTION
Manganese Reserves
Manganese Deposits – South Africa Pyrolusite – MnO2
South African Manganese Deposits World Manganese Production
Manganese Mine – North Cape, South Africa
Manganese Mine -China Manganese Mine - India
Manganese Mines - BRAZIL
INDIANMANGANESE SCENARIO:
India is the Sixth largest producer of Manganese in the world ; the South
Africa being the largest and China the second largest. The Ore deposits
presently being worked in India are located in Singhbhum(Jharkhand),
Panchmahals (Gujarat) , Balaghat (Madhya Pradesh), Vishakpatnam (Andhra
Pradesh), Sandur & Shimoga (Karnataka) , Bhandara and Nagpur
(Maharashtra), Bonai, Keonjhar and Koraput (Odisha), and Banswara
(Rajasthan).
The Total Manganese reserves according to Indian Bureau of Mines are
estimated to be 108 million tons. The total production of Manganese ores in
India was 1,774,000 tons; Odisha, Madhya Pradesh,Karnataka,and
Maharashtra accounting for 90 per cent of the production.
The Manganese ores found in India are generally mixtures of psilomelane
[Mn,Ba,Mn8O16(OH)2], braunite
(MnSiO2),pyrolusite(MnO2),hollandite(Mn,Ba,Mn6O14).
MANGANESEORE CATEGORIES:
Manganese ores can be classified into four categories , namely:
• SIMPLE ORES:
These ores contain small quantities of gangue materials that are amenable to
concentration by simple methods involving only ore treatments ,i.e. gravity
separation, magnetic separation ,or floatation.
• FERRUGINOUS ORES:
These ores not only contain iron minerals which can be removed by magnetizing
reduction roasting followed by magnetic separation.
• GARNETIFERROUS ORES:
These ores contain only garnets and quartz as the chief gangue minerals and can be
upgraded either by an electro-static separation method or by floatation.
• COMPLEX ORES:
These ores contain different type of gangue minerals in intimate association with
manganese minerals, and complicated treatment is required for their extraction.
VARIOUS MANGANESE MINERALS FOUND IN THE WORLD
• Borates: Sussexite ,Tusionite,
• Carbonates: Ankerite ,Kutnohorite ,Rhodochrosite ,Manganoan ,Calcite,
• Oxides:
1. Simple: Hausmannite ,Manganite ,Manganosite, Nsutite, Pyrolusite,
2. Mixed: Birnessite ,Bixbyite ,Ferrocolumbite ,Ferrotantalite ,Galaxite, Jacobsite, Manganotantalite, Psilomelane
,Romanèchite ,Tantalite ,Todorokite ,Umber.
• Phosphates:
Childrenite ,Graftonite, Lithiophilite ,Natrophilite, Purpurite ,Triplite ,Triploidite, Zanazziite.
• Silicates:
Babingtonite Bixbite ,Braunite, Brownleeite ,Calderite, Chloritoid ,Eudialyte ,Glaucochroite ,Jeffersonite Knebelite
,Ottrelite ,Piemontite Pyroxferroite, Rhodonite, Spessartine ,Sugilite, Tephroite, Zakharovite Zircophyllite.
• Sulfides:
Alabandite, Hauerite, Rambergite.
• Others:
Axinite (borosilicate), Geigerite (arsenate), Manganese nodule (various) ,Samsonite (Sulfosalt) Zincobotryogen
(sulfate), Wolframite Hübnerite
PYROLUSITE (MnO2)
PRODUCT Fe Mn SiO2 Al2O3 P S MOISTURE
LUMP 15-17 35-38 3.5-4.5 3-4 0.06-0.07 0.007-0.009 5-7
LUMP 13-15 38-40 2.5-3.5 2.5-3 0.06-0.07 0.007-0.008 5-7
LUMP 11-13 40-42 1.5-2.5 2-2.5 0.06-0.07 0.007-0.008 3-5
CHEMICAL COMPOSITION (in %) SIZE SPECIFICATION (in
%)
PYROLUSITE ORE SPECIFICATIONS IN ODISHA, INDIA
MANGANITE
PSILOMELANE ()
PSILOMELANE JWELLERYPSILOMELANE ORE
BRAUNITE
HOLLANDITE (Ba(Mn4+
6Mn3+
2)O16) ORE CONTAINING 35% Mn
RHODOCHROSITE (MnCO3) RHODONITE ((Mn2+,Fe2+,Mg,Ca)SiO3)
RHODONITE
SEDIMENTARY MANGANESE ORE
SEDIMENTARY MANGANESE CARBONATE
VOLCANIC MANGANESE ORES
POLYMETALIC MANGANESE OCEAN NODULES DISTRBN.
Manganese Nodule
MANGANESE OCEAN NODULES HARVESTING TECHNOLOGIES
MAGANESE OREPROCESSING
Beneficiation Processes Adopted vis-à-vis Impurities In Ores
Methods of Beneficiation:
• INTRODUCTION:
->Mechanical beneficiation of manganese ores is a must before metal extraction .
-> The various metallic ,non- metallic and volatile Impurities ,etc. are removed during the beneficiation
processes.
METALLIC IMPURITIES Fe,Pb,Cu,Zn,Ag
NON- METALLIC IMPURITIES Sulphur , Phosphorous
VOLATILE IMPURITIES H2O,CO2,Organic Matters
GANGUE SiO2,AL2O3,CaO,MgO,BaO
• PROCESSES:
 HAND SORTING & PICKING:
The various Ore Impurities from the water - washed ores are hand-picked from the moving Conveyor
belt in the processing plants.
 JIGGING:
Mechanically operated ,Air pulsating Jigs remove the gangue in a rising current of air from the valuable
heavier minerals which settle at the bottom ,used for beneficiating low grade Mn ores.
 TABLING:
The heavier mineral particles settling along the riffles are collected along the diagonal
line of the table and the lighter gangue particles are washed away with the effluent.
 HEAVY MEDIA SEPARATION:
When the fine ore particles are mixed to a heavy ferrosilicon in a water medium the
lighter gangue floats on the top and are separated from the heavier mineral particles
settling at the bottom, which is further washed to remove the adhering ferrosilicon from
it.
MAGNETIC SEPARATION:
The magnetic separator works by varying the magnetic field which separates the
mineral particles of different magnetic susceptibilities .
 ELECTROSTATIC SEPARATION:
The electro -static separator, separates the conducting and non-conducting particles
,where the conducting particles remain unaffected in the electric field and follow the
tangential path whereas the non- conducting particle remain pinned down to the rotor.
• Hydrometallurgical Process Of Beneficiation:
This process generally involves the dissolution of manganese ore with gaseous sulphur
dioxide in water( Sulphurus acid ) , sulphuric acid and ferrous sulphate, ammonium
sulphate with nitric acid or concentrated hydrochloric acid in order to remove iron, silica,
phosphorous and other impurities.
• Pyrometallurgical Process Of Beneficiation:
In this process, the low grade manganese ores are broken down by the action of heat.
Here the ores are agglomerated initially in order to make the size receptible for the
blast furnace.
Agglomeration process can be achieved by :
1. Briquetting
2. Sintering
3. Pelletising
4. Nodulising.
Agglomeration in brief:
Briquetting:
Here the fine particles are agglomerated by application of pressure , at temperature of
100 ̊C and pressure
of 4000 lb per square inch.
The most common machine used for this process is Double roll machine.
Sintering:
Sintering technique involves bonding of mineral particles by incipient fusion. This technique
is commonly applied for manganese ore fines having size of (-) 6mm. The sintering process
follows three main steps viz,
(i) Preparation of feed,
(ii) Fusion of the prepared layer of the raw materials on the sintering machine and
(iii) Cooling of the agglomerated mass.
MANGANESE ORE BRIQUETTE MAKING UNIT
Pelletising:
It is an advanced method of sintering where pellets instead of loose mix are fire and heat
hardened, by rolling them to form small spheres, known as the pellets.
Pelletising involves two basic steps, Balling and Firing. Pellets are proved to offer better
performance than sinters in the blast furnace.
The usual pellet size varies from10 mm to 25 mm.
Nodulising:
This processes involves incipient fusion of particles. This method requires continuous
movement between the charge and the equipment and is generally carried out in a rotary
kiln at a temperature of 1250 ̊C to 1370 ̊C.
Nodulising process is used for practically any fine size but the process nowadays is replaced
completely by pelletisation and sintering.
Manganese Ore Handling
MANGANESE ORE PROCESSING UNITS
MANGANESE MINE Manganese Ore Beneficiation unit
MANGANESE ORE TRUCKING & SHIPMENT
MANGANESE ORE HANDLING CONVEYER UNIT
MANGANESE METAL EXTRACTION:
 90% of Manganese metal production is consumed by the iron and steel industries (10 kg of Mn per metric ton of steel,13
million metric ton of Mn per year consumed for steel production).
 High grade Mn ore ( >35% Mn by wt.) is processed conventionally by high temperature roasting (800-1000 ̊ C) of Mn(III),
Mn(IV) ores to MnO for leaching with Sulphuric acid and subsequent Electrowinning to recover Manganese metal .
 Low grade ( < 35% Mn by wt.) Mn ores of Pyrolusite , Psilomelane, Wad (MnO2) etc. are treated with dissolved SO2 in
water (Sulphurous acid) leading to formation Manganese Sulphate (MnSO4) and Manganese Dithionate (MnS2O6)
known as REDUCTIVE LEACHING (American Manganese Process).
MnO2 + SO2 → MnSO4 ……………………..(1)
MnO2 + 2SO2 → MnS2O6 ……………………..(2)
 Leachate solution pregnant with Mn salts are separated from the tailings in a Leach thickener tank .
 Impurities like Al, As, SiO2, Zn are precipitated from the leachate by adjusting the pH of the solution to about 6 and
sparging air , to be polished in a sand filter to remove the precipitated impurities .
 Manganese carbonate (MnCO3) precipitation is achieved by treating the leachate solution with sodium carbonate.
MnSO4 + Na2CO3 → MnCO3 + Na2SO4 …………………… (3)
MnS2O6 + Na2CO3 → MnCO3 + Na2S2O6 ………..…………(4)
HYDROMETALLURGY AND ELECTROWINNING OF MANGANESE METAL
MANGANESE ORE LEACHING UNITS
 Solid, precipitated MnCO3 is further filtered and rinsed (from Na2SO4 and Na2S2O6) to produce clean MnCO3 to feed
the electrolytic solution.
 The purified MnCO3 solution is fed into the cathode compartment of the divided Electrowinning cell along with
recycled electrolyte containing MnSO4 and Sulphuric Acid , pH buffer (Ammonium Sulphate) and Sodium sulphite as
reducing agents to prevent any further oxidation of manganese.
 The spent Catholyte with lower Mn concentration is fed into the anode compartment of the Electrowinning cell.
The main electrochemical reactions are as follows:
Main Cathode Reaction:
Mn2+ + 2e- → Mn
Anode Reaction:
H2O → ½ O2 + 2H+ + 2e-
Net Reaction:
MnSO4 + H2O → Mn + H2SO4 + ½ O2
Side Cathodic Reaction:
2H2O + 2e- → H2 + 2OH-
MnCO3 CAKE & POWDER
MANGANESE ELECTROWINNING CELL
 The cathodic hydroxide (OH ̄)ion can cause manganese hydroxide precipitation on the cathode surface
which is prevented by pH buffer ammonium sulphate and proper concentration of MnCO3 in the
Catholyte .
 H2SO4 generated in the process is recycled to dissolve MnCO3.
 Electrowinning of Mn metal proceeds at about 60-70% of current efficiency.
 Anhydrous Na2SO4 from the leachate solution along with Na2S2O6 is recovered by crystallization on
cooling the solution , Nano -filtration and heating the precipitate at 40 ̊C for Na2SO4, 267 ̊C for Na2S2O6
and the recovered sulphur dioxide gas is recycled back to the leach tank.
 On Electrowinning 99.5% pure Manganese metal is deposited in layers of few millimetres thick on the
stainless steel cathode sheet.
 The Manganese metal coated cathodes are extracted from the Electrowinning cell periodically , and flakes
of Manganese metal deposits are removed by hammering.
 The Manganese metal flakes are heated to 500 ̊C to remove Hydrogen gas and produce 99.9% pure
Manganese metal.
MANGANESE METAL POWDER FROM ELECTRO WINNING
MANGANESE METAL FLAKES
PYROMETALLURGY OF MANGANESE METAL
 Smelting of high grade (> 35% Mn by wt.) ores in a Blast furnace / Electric arc furnace , along with coke
reduces the Manganese oxides(MnO2,Mn2O3,Mn3O4) by Carbon into Manganous oxide(MnO) which is
further reduced by carbon at higher temperature to manganese metal and carbon dioxide.
 Silicon dioxide combining with MNO can prevent metal production which is avoided by adding Basic Fluxes in
regulated manner like roasted limestone. The smelting temperature and the pH of the slag is controlled to
prevent formation of Silicon metal.
 High carbon Ferro-manganese alloys is produced containing upto 76 to 80 percent manganese, 12 to 15
percent Iron, up to 7.5 percent Carbon, and up to 1.2 percent Silicon.
 SilicoManganese alloy , containing 65 to 68 percent Manganese, 16 to 21 percent Silicon, and 1.5 to 2
percent Carbon, is produced by the smelting of slag from high-carbon ferromanganese or of manganese ore
with coke and a quartz flux.
 Medium and Low Carbon Ferromanganese is produced by Smelting Manganese ore , lime flux and coal along
with Silicomanganese in a furnace. The low carbon content of Silicomanganese is transferred to the final
ferromanganese product.
PLANT LAYOUT OF MANGANESE SMELTER
Manganese Ore Smelting –Blast Furnace Pouring of Hot Metal into Crucible
SMELTER EXHAUST FILTERING
ELECTRIC ARC FURNACE SCHEMA
MANGANESE SMELTING UNIT - SUBMERGED ARC FURNACE
MANGANESE SMELTING IN OPERATION IN SUBMERGED ARC FURNACE
MANGANESE
ALLOYMAKING
 High carbon ferromanganese is used for making Carbon steels. For low carbon steel making medium or low carbon
ferromanganese or electrolytic manganese are employed.
 Manganese metal desulphurizes the high melting sulphide particles i.e. preventing “the hot shortness – low heat
withstanding capacity” of carbon steels.
 As a Deoxidiser Silicomanganese is added to steel making.
 Manganese metal as an alloying agent to Carbon steel increases the metal strength , hardness , hardenability and
abrasion resistance (Hadfield steel- 10-14% Manganese ,wear- resistant).
 Low alloy (1.2% Mn) steel has increased tensile strength and increased steel yield.
FERROUS ALLOYS:
NON-FERROUS ALLOYS:
 Aluminium –manganese(2 %) alloy has greater tensile strength , wear resistance , corrosion resistance than pure
aluminium metal.
 Nickel, Zinc, Copper alloys with Manganese (Deoxidiser) , which lowers the Liquidus & Solidus of the alloy metal
thereby improving castability, improving strengthening effect, increasing electrical resistivity and thermal expansion
of the Alloy metal.
WORLD -WIDE MANGANESE - FERRO ALLOYS PRODUCTION
Ferro –Manganese Alloy Making
FERRO –MANGANESE ALLOY PRODUCTION AT A GLANCE
Ferro- Manganese Smelting Ferro –Manganese Metal Alloy
MANGANESECHEMICALS:
oMANGANOUS OXIDE (MnO) is used as a Fertilizer
and in speciality Ceramics.
oMnO2 is used as a Depolarizer in Dry -cell
Batteries which is produced by electrolysis.
oPotassium Permanganate (KMnO4) finds wide
usage as an Oxidising Agent, which is produced
by alkaline fusion and electrolysis.
CONCLUSION:
MANGANESE is a Steel –Grey Metal ,Hard but Brittle .
After IRON it is the next most Abundant Transition Metal on Earth.
SouthAfrica, China, Brazil, Australia, Gabon, India are the major Manganese
producer currently.
Pyrolusite is major Manganese Ore worldwide.
Manganese Ore Beneficiation is done regularly before Metal Extraction.
High grade ores are subjected to PyroMetallurgical & than HydroMetallurgical
process, ElectroWinning before Smelting for Metal extraction.
Low grade ores are subjected to HydroMetallurgical(American Manganese
Process) ,ElectroWinning & Smelting for Metal extraction.
Manganese is the most important ingredient in Carbon –Steel making of various
specifications.
Ferro-Manganese,Silico-Manganese, Ni,Cu, Zn, Al -Manganese Alloys of different
specifications are made to improve the Material properties of Alloy Metals to a
great deal for Modern requirements.
Manganese based Chemicals are widely used in various sectors of daily usage.
BIBILIOGRAPHY:
Wikipedia – the free Encyclopedia, Internet
resources.
Indian Bureau of Mines Survey Reports on
Manganese Mining & Extraction.
Indian Ocean Maganese Nodule field Geology
Reports.
Manganese Beneficiation at M O I L, MP.
Manganese Processing – Encyclopedia Britannica.
HydroMetallurgical Processing of Manganese Ores –
American Manganese Process Reports.
EXTRACTIVE METALLURGY- MANGANESE

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EXTRACTIVE METALLURGY- MANGANESE

  • 1. WELCOME TO EXTRACTIVE METALLURGY PRESENTATION ON: MANGANESE MANGANESE DEPOSITS – South Africa
  • 3. Soumya Sobhan Dash Department of Metallurgy and Material Engineering National Institute of Technology, ROURKELA, INDIA PRESENTED BY:
  • 4. INTRODUCTION  MANGANESE is an Important Metal (Mn – 25) with many Metal Alloys , in particular Stainless Steel.  The major Mineral Ore for Mn is Pyrolusite – MnO2( Manganese Dioxide).  J G Gahn (1774) was First to isolate Manganese metal by Reducing MnO2 with Carbon.  Manganese is the 12th most abundant Earth element.  Manganese Ores in nature are Pyrolusite(MnO2), Braunite, Psilomelane, Rhodocrosite etc.  South Africa produces 80% of World Manganese output.  Manganese Nodules on the Ocean floor are yet to be Harvested commercially profitably .  Ferro-Manganese Alloys are produced with MnO2 ore, iron ore &Carbon smelting in a Blast Furnace/ Electric Arc Furnace.  Iron free Manganese Alloys are produced by Leaching MnO2 Ores with H2SO4 soln. & subsequent Electrowinning process .  Heap Leaching of MnO2 Ores with Natural Gas at 850 ̊C & in presence of CO results in formation of MnO which is easily leached with H2SO4 & Fe(II) Iron to produce Iron Hydroxide & Elemental Manganese, to be Electrowinned into Manganese Metal.  Manganese is essential to Steel production by virtue of it’s Sulfur fixing, Deoxidizing &Alloying properties.  Steel containing 8-15% of Manganese results in High Tensile strength  Aluminium –Manganese Alloy (0.8-1.5% Mn) results in Galvanic Corrosion free Alloy used in Beverage cans.  Organo-metallic Manganese Tricarbonyl compound added to Unleaded Gasoline boosts Octane rating of Fuel.
  • 5. History: Metallic manganese was first isolated in 1774 by Johan Gottlieb Gahn, a Swedish mineralogist who reduced Pyrolusite, a manganese dioxide ore, with carbon. In 1856 Robert Forester Mushet, a British steelmaker, used manganese to improve the ability of steel produced by the Bessemer process to withstand rolling and forging at elevated temperatures. A tough wear-resistant steel containing approximately 12 percent manganese was developed in Sheffield, England, by Robert Abbott Hadfield in 1882. Ferromanganese was first smelted commercially in a blast furnace in 1875; electric-furnace production began in 1890. Pure manganese was not available commercially until 1941, following work on electrolysis conducted in the 1930s under S.M. Shelton at the U.S. Bureau of Mines. By the early 21st century, manganese production had expanded to several locations throughout the world, and Australia, South Africa, China, Gabon, and Brazil became the largest producers. Johan Gottlieb Gahn
  • 7. WORLD MANGANESE RESERVES & PRODUCTION Manganese Reserves
  • 8.
  • 9. Manganese Deposits – South Africa Pyrolusite – MnO2
  • 10. South African Manganese Deposits World Manganese Production
  • 11. Manganese Mine – North Cape, South Africa
  • 12. Manganese Mine -China Manganese Mine - India
  • 15.
  • 16. India is the Sixth largest producer of Manganese in the world ; the South Africa being the largest and China the second largest. The Ore deposits presently being worked in India are located in Singhbhum(Jharkhand), Panchmahals (Gujarat) , Balaghat (Madhya Pradesh), Vishakpatnam (Andhra Pradesh), Sandur & Shimoga (Karnataka) , Bhandara and Nagpur (Maharashtra), Bonai, Keonjhar and Koraput (Odisha), and Banswara (Rajasthan). The Total Manganese reserves according to Indian Bureau of Mines are estimated to be 108 million tons. The total production of Manganese ores in India was 1,774,000 tons; Odisha, Madhya Pradesh,Karnataka,and Maharashtra accounting for 90 per cent of the production. The Manganese ores found in India are generally mixtures of psilomelane [Mn,Ba,Mn8O16(OH)2], braunite (MnSiO2),pyrolusite(MnO2),hollandite(Mn,Ba,Mn6O14).
  • 17.
  • 19. Manganese ores can be classified into four categories , namely: • SIMPLE ORES: These ores contain small quantities of gangue materials that are amenable to concentration by simple methods involving only ore treatments ,i.e. gravity separation, magnetic separation ,or floatation. • FERRUGINOUS ORES: These ores not only contain iron minerals which can be removed by magnetizing reduction roasting followed by magnetic separation. • GARNETIFERROUS ORES: These ores contain only garnets and quartz as the chief gangue minerals and can be upgraded either by an electro-static separation method or by floatation. • COMPLEX ORES: These ores contain different type of gangue minerals in intimate association with manganese minerals, and complicated treatment is required for their extraction.
  • 20. VARIOUS MANGANESE MINERALS FOUND IN THE WORLD • Borates: Sussexite ,Tusionite, • Carbonates: Ankerite ,Kutnohorite ,Rhodochrosite ,Manganoan ,Calcite, • Oxides: 1. Simple: Hausmannite ,Manganite ,Manganosite, Nsutite, Pyrolusite, 2. Mixed: Birnessite ,Bixbyite ,Ferrocolumbite ,Ferrotantalite ,Galaxite, Jacobsite, Manganotantalite, Psilomelane ,Romanèchite ,Tantalite ,Todorokite ,Umber. • Phosphates: Childrenite ,Graftonite, Lithiophilite ,Natrophilite, Purpurite ,Triplite ,Triploidite, Zanazziite. • Silicates: Babingtonite Bixbite ,Braunite, Brownleeite ,Calderite, Chloritoid ,Eudialyte ,Glaucochroite ,Jeffersonite Knebelite ,Ottrelite ,Piemontite Pyroxferroite, Rhodonite, Spessartine ,Sugilite, Tephroite, Zakharovite Zircophyllite. • Sulfides: Alabandite, Hauerite, Rambergite. • Others: Axinite (borosilicate), Geigerite (arsenate), Manganese nodule (various) ,Samsonite (Sulfosalt) Zincobotryogen (sulfate), Wolframite Hübnerite
  • 22. PRODUCT Fe Mn SiO2 Al2O3 P S MOISTURE LUMP 15-17 35-38 3.5-4.5 3-4 0.06-0.07 0.007-0.009 5-7 LUMP 13-15 38-40 2.5-3.5 2.5-3 0.06-0.07 0.007-0.008 5-7 LUMP 11-13 40-42 1.5-2.5 2-2.5 0.06-0.07 0.007-0.008 3-5 CHEMICAL COMPOSITION (in %) SIZE SPECIFICATION (in %) PYROLUSITE ORE SPECIFICATIONS IN ODISHA, INDIA
  • 28. RHODOCHROSITE (MnCO3) RHODONITE ((Mn2+,Fe2+,Mg,Ca)SiO3)
  • 33. POLYMETALIC MANGANESE OCEAN NODULES DISTRBN. Manganese Nodule
  • 34. MANGANESE OCEAN NODULES HARVESTING TECHNOLOGIES
  • 36.
  • 37. Beneficiation Processes Adopted vis-à-vis Impurities In Ores
  • 38. Methods of Beneficiation: • INTRODUCTION: ->Mechanical beneficiation of manganese ores is a must before metal extraction . -> The various metallic ,non- metallic and volatile Impurities ,etc. are removed during the beneficiation processes. METALLIC IMPURITIES Fe,Pb,Cu,Zn,Ag NON- METALLIC IMPURITIES Sulphur , Phosphorous VOLATILE IMPURITIES H2O,CO2,Organic Matters GANGUE SiO2,AL2O3,CaO,MgO,BaO • PROCESSES:  HAND SORTING & PICKING: The various Ore Impurities from the water - washed ores are hand-picked from the moving Conveyor belt in the processing plants.  JIGGING: Mechanically operated ,Air pulsating Jigs remove the gangue in a rising current of air from the valuable heavier minerals which settle at the bottom ,used for beneficiating low grade Mn ores.
  • 39.  TABLING: The heavier mineral particles settling along the riffles are collected along the diagonal line of the table and the lighter gangue particles are washed away with the effluent.  HEAVY MEDIA SEPARATION: When the fine ore particles are mixed to a heavy ferrosilicon in a water medium the lighter gangue floats on the top and are separated from the heavier mineral particles settling at the bottom, which is further washed to remove the adhering ferrosilicon from it. MAGNETIC SEPARATION: The magnetic separator works by varying the magnetic field which separates the mineral particles of different magnetic susceptibilities .  ELECTROSTATIC SEPARATION: The electro -static separator, separates the conducting and non-conducting particles ,where the conducting particles remain unaffected in the electric field and follow the tangential path whereas the non- conducting particle remain pinned down to the rotor.
  • 40. • Hydrometallurgical Process Of Beneficiation: This process generally involves the dissolution of manganese ore with gaseous sulphur dioxide in water( Sulphurus acid ) , sulphuric acid and ferrous sulphate, ammonium sulphate with nitric acid or concentrated hydrochloric acid in order to remove iron, silica, phosphorous and other impurities. • Pyrometallurgical Process Of Beneficiation: In this process, the low grade manganese ores are broken down by the action of heat. Here the ores are agglomerated initially in order to make the size receptible for the blast furnace. Agglomeration process can be achieved by : 1. Briquetting 2. Sintering 3. Pelletising 4. Nodulising.
  • 41. Agglomeration in brief: Briquetting: Here the fine particles are agglomerated by application of pressure , at temperature of 100 ̊C and pressure of 4000 lb per square inch. The most common machine used for this process is Double roll machine. Sintering: Sintering technique involves bonding of mineral particles by incipient fusion. This technique is commonly applied for manganese ore fines having size of (-) 6mm. The sintering process follows three main steps viz, (i) Preparation of feed, (ii) Fusion of the prepared layer of the raw materials on the sintering machine and (iii) Cooling of the agglomerated mass.
  • 42. MANGANESE ORE BRIQUETTE MAKING UNIT
  • 43. Pelletising: It is an advanced method of sintering where pellets instead of loose mix are fire and heat hardened, by rolling them to form small spheres, known as the pellets. Pelletising involves two basic steps, Balling and Firing. Pellets are proved to offer better performance than sinters in the blast furnace. The usual pellet size varies from10 mm to 25 mm. Nodulising: This processes involves incipient fusion of particles. This method requires continuous movement between the charge and the equipment and is generally carried out in a rotary kiln at a temperature of 1250 ̊C to 1370 ̊C. Nodulising process is used for practically any fine size but the process nowadays is replaced completely by pelletisation and sintering.
  • 45.
  • 47. MANGANESE MINE Manganese Ore Beneficiation unit
  • 49. MANGANESE ORE HANDLING CONVEYER UNIT
  • 50.
  • 52.  90% of Manganese metal production is consumed by the iron and steel industries (10 kg of Mn per metric ton of steel,13 million metric ton of Mn per year consumed for steel production).  High grade Mn ore ( >35% Mn by wt.) is processed conventionally by high temperature roasting (800-1000 ̊ C) of Mn(III), Mn(IV) ores to MnO for leaching with Sulphuric acid and subsequent Electrowinning to recover Manganese metal .  Low grade ( < 35% Mn by wt.) Mn ores of Pyrolusite , Psilomelane, Wad (MnO2) etc. are treated with dissolved SO2 in water (Sulphurous acid) leading to formation Manganese Sulphate (MnSO4) and Manganese Dithionate (MnS2O6) known as REDUCTIVE LEACHING (American Manganese Process). MnO2 + SO2 → MnSO4 ……………………..(1) MnO2 + 2SO2 → MnS2O6 ……………………..(2)  Leachate solution pregnant with Mn salts are separated from the tailings in a Leach thickener tank .  Impurities like Al, As, SiO2, Zn are precipitated from the leachate by adjusting the pH of the solution to about 6 and sparging air , to be polished in a sand filter to remove the precipitated impurities .  Manganese carbonate (MnCO3) precipitation is achieved by treating the leachate solution with sodium carbonate. MnSO4 + Na2CO3 → MnCO3 + Na2SO4 …………………… (3) MnS2O6 + Na2CO3 → MnCO3 + Na2S2O6 ………..…………(4) HYDROMETALLURGY AND ELECTROWINNING OF MANGANESE METAL
  • 54.  Solid, precipitated MnCO3 is further filtered and rinsed (from Na2SO4 and Na2S2O6) to produce clean MnCO3 to feed the electrolytic solution.  The purified MnCO3 solution is fed into the cathode compartment of the divided Electrowinning cell along with recycled electrolyte containing MnSO4 and Sulphuric Acid , pH buffer (Ammonium Sulphate) and Sodium sulphite as reducing agents to prevent any further oxidation of manganese.  The spent Catholyte with lower Mn concentration is fed into the anode compartment of the Electrowinning cell. The main electrochemical reactions are as follows: Main Cathode Reaction: Mn2+ + 2e- → Mn Anode Reaction: H2O → ½ O2 + 2H+ + 2e- Net Reaction: MnSO4 + H2O → Mn + H2SO4 + ½ O2 Side Cathodic Reaction: 2H2O + 2e- → H2 + 2OH-
  • 55. MnCO3 CAKE & POWDER
  • 57.  The cathodic hydroxide (OH ̄)ion can cause manganese hydroxide precipitation on the cathode surface which is prevented by pH buffer ammonium sulphate and proper concentration of MnCO3 in the Catholyte .  H2SO4 generated in the process is recycled to dissolve MnCO3.  Electrowinning of Mn metal proceeds at about 60-70% of current efficiency.  Anhydrous Na2SO4 from the leachate solution along with Na2S2O6 is recovered by crystallization on cooling the solution , Nano -filtration and heating the precipitate at 40 ̊C for Na2SO4, 267 ̊C for Na2S2O6 and the recovered sulphur dioxide gas is recycled back to the leach tank.  On Electrowinning 99.5% pure Manganese metal is deposited in layers of few millimetres thick on the stainless steel cathode sheet.  The Manganese metal coated cathodes are extracted from the Electrowinning cell periodically , and flakes of Manganese metal deposits are removed by hammering.  The Manganese metal flakes are heated to 500 ̊C to remove Hydrogen gas and produce 99.9% pure Manganese metal. MANGANESE METAL POWDER FROM ELECTRO WINNING
  • 59. PYROMETALLURGY OF MANGANESE METAL  Smelting of high grade (> 35% Mn by wt.) ores in a Blast furnace / Electric arc furnace , along with coke reduces the Manganese oxides(MnO2,Mn2O3,Mn3O4) by Carbon into Manganous oxide(MnO) which is further reduced by carbon at higher temperature to manganese metal and carbon dioxide.  Silicon dioxide combining with MNO can prevent metal production which is avoided by adding Basic Fluxes in regulated manner like roasted limestone. The smelting temperature and the pH of the slag is controlled to prevent formation of Silicon metal.  High carbon Ferro-manganese alloys is produced containing upto 76 to 80 percent manganese, 12 to 15 percent Iron, up to 7.5 percent Carbon, and up to 1.2 percent Silicon.  SilicoManganese alloy , containing 65 to 68 percent Manganese, 16 to 21 percent Silicon, and 1.5 to 2 percent Carbon, is produced by the smelting of slag from high-carbon ferromanganese or of manganese ore with coke and a quartz flux.  Medium and Low Carbon Ferromanganese is produced by Smelting Manganese ore , lime flux and coal along with Silicomanganese in a furnace. The low carbon content of Silicomanganese is transferred to the final ferromanganese product.
  • 60. PLANT LAYOUT OF MANGANESE SMELTER
  • 61. Manganese Ore Smelting –Blast Furnace Pouring of Hot Metal into Crucible
  • 64. MANGANESE SMELTING UNIT - SUBMERGED ARC FURNACE
  • 65. MANGANESE SMELTING IN OPERATION IN SUBMERGED ARC FURNACE
  • 67.  High carbon ferromanganese is used for making Carbon steels. For low carbon steel making medium or low carbon ferromanganese or electrolytic manganese are employed.  Manganese metal desulphurizes the high melting sulphide particles i.e. preventing “the hot shortness – low heat withstanding capacity” of carbon steels.  As a Deoxidiser Silicomanganese is added to steel making.  Manganese metal as an alloying agent to Carbon steel increases the metal strength , hardness , hardenability and abrasion resistance (Hadfield steel- 10-14% Manganese ,wear- resistant).  Low alloy (1.2% Mn) steel has increased tensile strength and increased steel yield. FERROUS ALLOYS: NON-FERROUS ALLOYS:  Aluminium –manganese(2 %) alloy has greater tensile strength , wear resistance , corrosion resistance than pure aluminium metal.  Nickel, Zinc, Copper alloys with Manganese (Deoxidiser) , which lowers the Liquidus & Solidus of the alloy metal thereby improving castability, improving strengthening effect, increasing electrical resistivity and thermal expansion of the Alloy metal.
  • 68. WORLD -WIDE MANGANESE - FERRO ALLOYS PRODUCTION
  • 70. FERRO –MANGANESE ALLOY PRODUCTION AT A GLANCE
  • 71. Ferro- Manganese Smelting Ferro –Manganese Metal Alloy
  • 72. MANGANESECHEMICALS: oMANGANOUS OXIDE (MnO) is used as a Fertilizer and in speciality Ceramics. oMnO2 is used as a Depolarizer in Dry -cell Batteries which is produced by electrolysis. oPotassium Permanganate (KMnO4) finds wide usage as an Oxidising Agent, which is produced by alkaline fusion and electrolysis.
  • 73.
  • 74. CONCLUSION: MANGANESE is a Steel –Grey Metal ,Hard but Brittle . After IRON it is the next most Abundant Transition Metal on Earth. SouthAfrica, China, Brazil, Australia, Gabon, India are the major Manganese producer currently. Pyrolusite is major Manganese Ore worldwide. Manganese Ore Beneficiation is done regularly before Metal Extraction. High grade ores are subjected to PyroMetallurgical & than HydroMetallurgical process, ElectroWinning before Smelting for Metal extraction. Low grade ores are subjected to HydroMetallurgical(American Manganese Process) ,ElectroWinning & Smelting for Metal extraction. Manganese is the most important ingredient in Carbon –Steel making of various specifications. Ferro-Manganese,Silico-Manganese, Ni,Cu, Zn, Al -Manganese Alloys of different specifications are made to improve the Material properties of Alloy Metals to a great deal for Modern requirements. Manganese based Chemicals are widely used in various sectors of daily usage.
  • 75. BIBILIOGRAPHY: Wikipedia – the free Encyclopedia, Internet resources. Indian Bureau of Mines Survey Reports on Manganese Mining & Extraction. Indian Ocean Maganese Nodule field Geology Reports. Manganese Beneficiation at M O I L, MP. Manganese Processing – Encyclopedia Britannica. HydroMetallurgical Processing of Manganese Ores – American Manganese Process Reports.