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Manganese (Mn) is a brittle, hard gray white to silvery metal that looks much
like iron. As an essential ingredient of steel, manganese is the 12th most
abundant element widely distributed in the earth’s crust and the 4th most used
metal in terms of tonnage, ranked after iron, aluminium and copper.
Nevertheless it is only rarely found in concentrations high enough to form a
manganese ore deposit. Among some 300 minerals containing manganese, only
a dozen are of mining significance. Mn never occurs as the native metal in
nature, but exists in the form of oxides, carbonates and silicates in the earth’s
crust. Approximately 95% of total production of Mn ore is consumed in
steelmaking because of its sulphur fixing, deoxidizing, and alloying properties,
to form ferromanganese-alloys (Acharya et al., 2004). Without manganese,
steel would not be able to achieve the tensile strength, toughness, stiffness,
wear resistance and hardness that make it such a useful engineering material.
Moreover use of manganese in inadequate quantities in the steelmaking process
would result in cracks during hot rolling or forging. In addition to its use as an
alloy in steel and cast iron, manganese is also employed as an alloy (in very
much lesser quantities) with aluminium, copper, nickel, titanium and zinc. It is
also used in minor quantities for electronic applications, along with either,
bismuth, gold and silver.
Apart from the above mentioned applications there are numerous chemical
applications of manganese oxide and salts. Potassium permanganate is one of
the best known manganese products. It is a powerful oxidizing agent with
bactericidal and algicidal properties, which enable it to be used in purifying
drinking water and treating waste water (Banerjee 1950). It is also used for
odor control, including deodorization of discharges from paint factories, fish
processing plants etc. Permanganate has a variety of other applications as an
oxidant. An important application for manganese is Maneb (manganese
ethylene bisdithiocarbamate), an organo chemical compound sold in the form
of a yellow powder, which is an agricultural fungicide and is widely used for
controlling crop and cereal diseases (Rhodes 1977). An organic manganese
compound known as MMT (methylcyclo pentadienyl manganese tricarbonyl) is
used on a small scale as an octane booster or anti knock agent in gasoline
(Hamadi 2010). MMT can dramatically improve oil combustion, reducing
boiler clogging and soot levels. This application is important from an
environmental point of view as it allows lead to be replaced, but it has not yet
been fully developed (Strikkers 2002). Manganese dioxide is used as a catalyst
in the production of artificial flavours like vanilla. It is also used as an
oxidizing agent in treating uranium ore to produce the oxide concentrate known
as “yellow cake” (Zhang Jianguo et. Al 2004). Other applications include the
colouring of bricks and tiles, paint driers and as a pigment for paints, etc.
Manganese sulphate is widely used as an end product in fertilizers and animal
feed, and as an intermediate product in the chemical industry. Manganese
phosphatation is used to produce surface films which, when sealed with oil or
wax, can protect steels for internal or mild outdoor use. Thus, Manganese
phosphating improves wear resistance, prevents welding of metals under load,
increases lubrication efficiency by oil absorption and assures rapid and safe
running of moving parts. Another important material is manganese ferrite, a
soft ferrite widely used in electronics. Large amounts are consumed in the
manufacture of television circuit boards. Manganese for this purpose can come
from ore, oxides, carbonates and even metallic manganese. Manganese is also
used in the process of making electrolytic zinc. In the presence of MnO2, zinc
sulphide concentrates are processed with sulphuric acid. The effect during this
leaching process gives 99% extraction of zinc, 98% of manganese, and 96%
liberation of elemental sulphur.
The low grade bimetallic ores from Sandur are important on account of their
relative abundance and good export market. Their low silica and phosphorous
content add to their importance because of their suitability for blending with
high grade ores with having high phosphorous content.
High grade manganese ores are typically processed into suitable metallic alloy
formed by pyrometallurgical processes. The nonferrous gangue minerals can be
removed easily by gravity separation techniques but separation of near density
iron minerals requires high intensity magnetic separator or reduction roasting
process to achieve a high Mn/Fe ratio in the concentrate (Narayanan and
Subramanian, 1959; Mohanty et al., 1981; Huaming and Guanzhou, 1998;
Singh et al., 2011).
In order to beneficiate the low grade Mn ores of Sandur Schist Belt, the author
has carried out ore microscopic studies to know the major and accessary
minerals as well as ore and gangue minerals present in the ore samples.
Geochemical investigation of the ore samples was carried out to determine the
concentration of major and minor minerals as well as REE’s. IR and DTA-
TGA studies were carried out to identify the other minerals which cannot be
identified with ore microscopic studies. After confirming the presence of
minerals in the samples with various physical and chemical tools, beneficiation
studies were taken up. In beneficiation studies Comminution, liberation and
sizing and screening studies were carried out. The Mn % was observed to be
upgraded by 1-1.5% after screening with 97-99% recovery. The results are
discussed in detail in the respective chapter.
Previous work
The area under investigation Sandur Schist Belt is a part of Sandur taluk,
Bellary district, Karnataka state (Fig. 1.1) and is bound by latitude 14°55’ to
15°15’N and longitude 76°20’ to 76°40’E, it is included in Survey of India
toposheet nos. 57 B/3,57 A/8 and 57 A/12. The area is marked by several active
mines for manganese and iron ores and is well connected by a number of fair
weather roads.
Kudlgi and Torangallu are connected by the state highway no. 40 passing
through Sandur. Torangallu is the site where ‘Jindal Vijayanagar steel Limited’
(JVSL) is located and is 30 Km from Sandur.
M/s. Sandur Manganese and Iron Ores Ltd. (SMIORE) hold lease over an area
of 50 sq. Km in Deogiri, Subrayanhalli and Ramandurg ranges, which covers
almost entire area of manganese mineralization of the schist belt.
Fig. 1.1- Location map of Sandur
Fig. 1.2- Sandur Schist Belt location and boundary on Satellite Imagery
Physiography and Drainage of the area
Topography of the region is distinct and unique, the hills of Sandur rise above
the plain topography of the surrounding. The Sandur Schist Belt is marked by
elongated hill ranges running in NNW-SSE direction. This is the result of
structural manifestation of the rocks coupled with weathering agents.
The entire schist belt is trending nearly NW-SE with a length of 53 Kms
(Parallel to strike direction) and spreading over an area of 600 sq. kms. The
central part of schist belt is a valley flanked by hill ranges extending both sides
(NW-SE) with diminishing width. The schist belt is surrounded by granitoids.
Most of the area in the central part of the Sandur valley is plain and has a R.L.
of 500-600 m above MSL, while the hills rise to over 1000 m the highest point
is on Hirray Gutti peak of Kumarswamy range with a R.L. of 1105 m above
MSL. As a result of lateritization, the hills have given rise to flat tops which are
described as plateaus. The change in elevation is abrupt. A perennial river
Narihalla, flows west to East in the area. Kumarswamy range is in the south of
Narihalla, whereas, Ramgad range is to the north. The area has various springs
at several points like Harishankar, Byrethirtha and Ramgad.
The Sandur Schist Belt is one of the important greenstone belts of Karnataka
Craton and is named after the town Sandur where it is typically exposed. The
rich manganese ore deposits associated with the schist belt have evoked interest
of economic geologists, mining engineers and metallurgist since long as
evidenced by numerous old workings.
The Sandur Schist Belt forms parts of Dharwar Supergroup. The schist belt is
represented by a thick pile of volcano-sedimentary sequence in which the
volcanic component predominates (fig. 1.3). The entire succession rests
unconfirmably over the granitic gneisses and is intruded by younger granites of
the Closepet. The volcanic suite is represented predominantly by metabasalts
and the associated basic pyroclasts, with subordinate intermediate and acid
lavas. The metasediments are constituted by orthoquartzite, limestone,
manganiferous chert, argillite, wacke, and banded iron formation.
The Sandur Schist Belt comprises of basic igneous rocks (metabasalts and
pillow lava), ferruginous and manganiferous phyllite/shale, younger intrusive
banded ferruginous quartzite, iron and manganese ores and laterite.
Methods of Investigation
Literature review- The study area was delineated from the geological map of
Karnataka. Toposheets of the respective area were collected. Available
literature and previous work done was studied carefully and reviewed before
starting of actual research work, to decide the course of the research work.
Sampling- Working and abandoned mining pits were sampled for Mn ore
samples. Systematic sampling was carried out. Samples were collected from
various working and abandoned mining sections of Deogiri, SB Halli, and
Ramgad sections. The samples were collected in such way that they represent
all the lithologies associated with Mn mineralization in the area under
investigation. Field photographs were taken for better representation of the
information collected during the field work.
Geochemistry- Twenty five samples are crushed and reduced to fine powder
and analyzed in the laboratory to find out major oxides such as MnO2, Fe2O3,
SiO2, Al2O3, P2O5, CaO and MgO.
Fourteen samples are analyzed for trace elements to find out the concentration
of Cu, Co, Ni, Zn, Pb and Cr along with MnO2 and Fe2O3.
Five samples are subjected for REE and trace elements and the contents are
reported in ppm. The elements analyzed are LREE i.e. Lanthanum (La),
Cerium (Ce), Praseodymium (Pr), Neodymium (Nd), Samarium (Sm) and
Europium (Eu). HREE elements were also analyzed i.e. Gadolinium (Gd),
Dysprosium (Dy), Erbium (Er), Ytterbium (Yb) and Lutetium (Lu). Along with
LREE and HREE, Yttrium (Y), Thorium(Th), Uranium (U), Hafnium (Hf),
Zirconium (Zr), Cesium (Cs), Tantalum (Ta), Scandium (Sc), Niobium (Nb),
Gallium (Ga), Vanadium (V), Strontium (Sr) and Rubidium (Rb) these trace
elements are analyzed.
Indian manganese ores are preferred by many as they are generally hard, lumpy
and amenable to easy reduction. In the Indian continent, the deposition of
manganese must have taken place in varying environmental settings and by
different geological processes but the sedimentary mode of formation far
outweighed other methods such as supergene enrichment etc. These manganese
ores have been selectively exploited either for direct use or for sweetening the
otherwise available phosphor-rich ores. Favourable geological and
geomorphologic settings, existing well connected rail and road links, easy
amenability of ores to beneficiation and liberal Govt. policies make the
exploitation of Indian manganese deposits practically a no risk proposition.
India is now the world’s fifth largest producer of manganese ore as per World
Manganese Organization report for 2012. It is estimated that about 20% of the
world’s manganese deposits are in India which makes India the seventh country
among largest manganese deposits. The important deposits lie in the states of
Madhya Pradesh, Maharashtra, Karnataka, Odisha, Gujarat, Rajasthan and Goa.
(Fig. 1.4)
The greenstone hosted manganese deposits are older in age and have general
close association of Banded Iron Formation such as in the Dharwarian rocks of
Karnataka and Goa as also the Iron Ore Supergroup of Orissa, namely in
Benai-Keonjhar tracts of North Orissa. As the time sequence changes over
from Archaean to Proterozoic, both the Khondalite-hosted ores (called as
Koduritic in classic literature, Fermor, 1909) as well as the Adilabad beds of
ore with the Penganga sequence, manifesting with practically no association of
iron or BIF, indicate progressive separation of iron or BIF, from manganese.
The total resources of manganese ore in the country as on April 2010 are
placed at 430 million tonnes as per UNFC system. Out of these, 142 million
tonnes are categorized as reserves and the balance 288 million tonnes are in the
remaining resources category (IBM Yearbook, 2012). Gradewise, ferro-
manganese grade accounts for 8%, medium grade 11%, BF grade 34% and the
remaining 47% are of mixed, low, others, unclassified, and not-known grades
including 0.35 million tonnes of battery/chemical grade. State wise, Odisha
tops the total resources with 44% share followed by Karnataka 22%, Madhya
Pradesh 13%, Maharashtra 8%, Andhra Pradesh 4% and Jharkhand and Goa
3% each (Fig 1.2). Rajasthan, Gujarat and West Bengal together shared the
remaining about 3% resources (Table – 1.1).
Production of manganese ore in India during 2011-12 was 2.6 million tonnes.
MOIL Ltd. was the largest producer of manganese ore with the share of 40% of
the total production followed by Tata Steel, SMIORE, OMC, Adhunik and
Rungta (IBM Yearbook, 2012) (Fig. 1.3).
Fig. 1.5- State wise manganese resources of India
Australia 93000
Brazil 110000
China 44000
Gabon 21000
India 56000
Mexico 4000
Ukraine 140000
The world manganese ore production for the year 2010 was 47.21 million
tonnes, as compared to 35.41 million tonnes during the year 2009 – up by
33.32% indicating strong growth in availability. About 95% of the world’s
production of manganese ore is used directly or indirectly in steel making and
other metallurgical usages.