Information about Manganese Nodule
Polymetallic nodules, also called manganese nodules, are rock concretions on the sea bottom formed of concentric layers of iron and manganese hydroxides around a core.
The core may be microscopically small and is sometimes completely transformed into manganese minerals by crystallization.
When visible to the naked eye, it can be a small test (shell) of a microfossil (radiolarian or foraminifer), a phosphatized shark tooth, basalt debris or even fragments of earlier nodules.
Nodules vary in size from tiny particles visible only under a microscope to large pellets more than 20 centimeters across. However, most nodules are between 5 and 10 cm in diameter, about the size of potatoes. Their surface is generally smooth, sometimes rough, mammilated (knobby) or otherwise irregular. The bottom, buried in sediment, is generally rougher than the top.
The chemical composition of nodules varies according to the kind of manganese minerals and the size and characteristics of the core. Those of greatest economic interest contain manganese (27-30 %), nickel (1.25-1.5 %), copper (1-1.4 %) and cobalt (0.2-0.25 %). Other constituents include iron (6 %), silicon (5%) and aluminum (3%), with lesser amounts of calcium, sodium, magnesium, potassium, titanium and barium, along with hydrogen and oxygen.
Polymetallic nodules were discovered in 1868 in the Kara Sea, in the Arctic Ocean off Siberia. During the scientific expeditions of the H.M.S. Challenger (1872-76), they were found to occur in most oceans of the world. Nodules of economic interest have been found in three areas: the north central Pacific Ocean, the Peru Basin in the southeast Pacific, and the center of the north Indian Ocean. The most promising of these deposits in terms of nodule abundance and metal concentration occur in the Clarion-Clipperton Fracture Zone of the eastern equatorial Pacific between Hawaii and Central America.
In the mid-seventies, a $70-million international joint venture succeeded in collecting multi-ton quantities of manganese nodules from the abyssal plains (18,000 feet, 5.5 km + depth) of the eastern equatorial Pacific Ocean. Significant quantities of nickel (the primary target) as well as copper and cobalt were subsequently extracted from this "ore" using both pyro and hydro methods. In the course of this 8-year project, a number of ancillary developments evolved, including the use of near-bottom towed side-scan sonar array to assay the nodule population density on the abyssal silt whilst simultaneously performing a sub-bottom profile with a derived, vertically-oriented, low-frequency acoustic beam.
The technology and art developed during the course of this project were never commercialized because the last two decades of the 20th century saw a glut of nickel production. The estimated $3.5-billion (1978 US dollars) investment to implement commercialization was an additional factor. Sumitomo Metal Mining continues to maintain a small (place-keeping) organization in this field.
A company by the name of Kennecott Copper had explored the potential profits in manganese nodule mining and found that it wasn't worth the cost. Other than the environmental issues and the fact that the profits had to be shared, there was not any cheap way to get the manganese nodules off the sea floor.
In the meantime, interest in the extraction of nodules had waned. Three factors were largely responsible: the difficulty and expense of developing and operating mining technology that could economically remove the nodules from depths of five or six kilometers and transport them to the ocean surface, the high taxes the international community would charge for the mining, and the continuing availability of the key minerals from land-based sources at market prices. The commercial extraction of polymetallic nodules is not considered likely to occur during the next two decades.
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Nodules vary in size from tiny particles visible only under a microscope to large pellets more than 20 centimeters across. However, most nodules are between 5 and 10 cm in diameter, about the size of potatoes. Their surface is generally smooth, sometimes rough, mammilated (knobby) or otherwise irregular. The bottom, buried in sediment, is generally rougher than the top.
Growth and composition
Nodule growth is one of the slowest of all geological phenomena – in the order of a centimeter over several million years. Several processes are involved in the formation of nodules, including the precipitation of metals from seawater (hydrogenous), the remobilization of manganese in the water column (diagenetic), the derivation of metals from hot springs associated with volcanic activity (hydrothermal), the decomposition of basaltic debris by seawater (halmyrolitic) and the precipitation of metal hydroxides through the activity of microorganisms (biogenic). Several of these processes may operate concurrently or they may follow one another during the formation of a nodule.The chemical composition of nodules varies according to the kind of manganese minerals and the size and characteristics of the core. Those of greatest economic interest contain manganese (27-30 %), nickel (1.25-1.5 %), copper (1-1.4 %) and cobalt (0.2-0.25 %). Other constituents include iron (6 %), silicon (5%) and aluminum (3%), with lesser amounts of calcium, sodium, magnesium, potassium, titanium and barium, along with hydrogen and oxygen.
Occurrence
Nodules lie on the seabed sediment, often partly or completely buried. They vary greatly in abundance, in some cases touching one another and covering more than 70 per cent of the bottom. The total amount of polymetallic nodules on the sea floor was estimated at 500 billion tons by A.A. Archer in 1981. They can occur at any depth, even in lakes, but the highest concentrations have been found on vast abyssal plains in the deep ocean between 4,000 and 6,000 meters.Polymetallic nodules were discovered in 1868 in the Kara Sea, in the Arctic Ocean off Siberia. During the scientific expeditions of the H.M.S. Challenger (1872-76), they were found to occur in most oceans of the world. Nodules of economic interest have been found in three areas: the north central Pacific Ocean, the Peru Basin in the southeast Pacific, and the center of the north Indian Ocean. The most promising of these deposits in terms of nodule abundance and metal concentration occur in the Clarion-Clipperton Fracture Zone of the eastern equatorial Pacific between Hawaii and Central America.
Mining
Interest in the potential exploitation of polymetallic nodules generated a great deal of activity among prospective mining consortia in the 1960s and 1970s. Almost half a billion dollars was invested in identifying potential deposits and in research and development of technology for mining and processing nodules. These initial undertakings were carried out primarily by four multinational consortia composed of companies from the United States, Canada, the United Kingdom, the Federal Republic of Germany, Belgium, the Netherlands, Italy, Japan and two groups of private companies and agencies from France and Japan. There were also three publicly sponsored entities from the Soviet Union, India and China.In the mid-seventies, a $70-million international joint venture succeeded in collecting multi-ton quantities of manganese nodules from the abyssal plains (18,000 feet, 5.5 km + depth) of the eastern equatorial Pacific Ocean. Significant quantities of nickel (the primary target) as well as copper and cobalt were subsequently extracted from this "ore" using both pyro and hydro methods. In the course of this 8-year project, a number of ancillary developments evolved, including the use of near-bottom towed side-scan sonar array to assay the nodule population density on the abyssal silt whilst simultaneously performing a sub-bottom profile with a derived, vertically-oriented, low-frequency acoustic beam.
The technology and art developed during the course of this project were never commercialized because the last two decades of the 20th century saw a glut of nickel production. The estimated $3.5-billion (1978 US dollars) investment to implement commercialization was an additional factor. Sumitomo Metal Mining continues to maintain a small (place-keeping) organization in this field.
Legal developments
The promise of nodule exploitation was one of the main factors that led developing nations to propose that the deep seabed beyond the limits of national jurisdiction should be treated as a “common heritage of mankind”, with proceeds to be shared between those who developed this resource and the rest of the international community. This initiative eventually resulted in the adoption (1982) of the United Nations Convention on the Law of the Sea and the establishment (1994) of the International Seabed Authority, with responsibility for controlling all deep-sea mining in international areas. The first legislative achievement of this intergovernmental organization was the adoption (2000) of regulations for prospecting and exploration for polymetallic nodules, with special provisions to protect the marine environment from any adverse effects. The Authority followed this up (2001-2002) by signing 15-year contracts with seven private and public entities, giving them exclusive rights to explore for nodules in specified tracts of the seabed, each 75,000 square kilometers in size. The United States, whose companies were among the key actors in the earlier period of exploration, remains outside this compact as a non-party to the Law of the Sea Convention.A company by the name of Kennecott Copper had explored the potential profits in manganese nodule mining and found that it wasn't worth the cost. Other than the environmental issues and the fact that the profits had to be shared, there was not any cheap way to get the manganese nodules off the sea floor.
In the meantime, interest in the extraction of nodules had waned. Three factors were largely responsible: the difficulty and expense of developing and operating mining technology that could economically remove the nodules from depths of five or six kilometers and transport them to the ocean surface, the high taxes the international community would charge for the mining, and the continuing availability of the key minerals from land-based sources at market prices. The commercial extraction of polymetallic nodules is not considered likely to occur during the next two decades.
See also
External link
Further reading
- Cronan, D. S. (1980). Underwater Minerals. London: Academic Press.
- Cronan, D. S. (2000). Handbook of Marine Mineral Deposits. Boca Raton: CRC Press.
- Cronan, D. S. (2001). "Manganese nodules." p. 1526-1533 in Encyclopedia of Ocean Sciences, J. Steele, K. Turekian and S. Thorpe, eds. San Diego: Academic Press.
- Earney, F.C. (1990). Marine Mineral Resources. London: Routledge.
- Roy, S. (1981). Manganese Deposits. London: Academic Press.
- Teleki, P.G., M.R. Dobson, J.R. Moore and U. von Stackelberg (eds). (1987). Marine Minerals: Advances in Research and Resource Assessment. Dordrecht: D. Riedel.
The three-letter acronym SEA may refer to:
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- Scientists and Engineers for America, a pro-science political advocacy group.
- Schoof-Elkies-Atkin algorithm
- Seattle-Tacoma International Airport (IATA: SEA, ICAO: KSEA)
- Sea Education Association
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3, 4, 6
(amphoteric oxide)
Electronegativity 1.83 (Pauling scale)
Ionization energies
(more) 1st: 762.5 kJmol−1
2nd: 1561.9 kJmol−1
3rd: 2957 kJmol−1
Atomic radius 140 pm
Atomic radius (calc.
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(amphoteric oxide)
Electronegativity 1.83 (Pauling scale)
Ionization energies
(more) 1st: 762.5 kJmol−1
2nd: 1561.9 kJmol−1
3rd: 2957 kJmol−1
Atomic radius 140 pm
Atomic radius (calc.
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2, 3
(oxides: acidic, basic or amphoteric
depending on the oxidation state)
Electronegativity 1.55 (Pauling scale)
Ionization energies
(more) 1st: 717.3 kJmol−1
2nd: 1509.
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(oxides: acidic, basic or amphoteric
depending on the oxidation state)
Electronegativity 1.55 (Pauling scale)
Ionization energies
(more) 1st: 717.3 kJmol−1
2nd: 1509.
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In chemistry, hydroxide is the most common name for the diatomic anion OH−, consisting of oxygen and hydrogen atoms, usually derived from the dissociation of a base. It is one of the simplest diatomic ions known.
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Crystallization is the (natural or artificial) process of formation of solid crystals from a uniform solution. Crystallization is also a chemical solid-liquid separation technique, in which mass transfer of a solute from the liquid solution to a pure solid crystalline phase occurs.
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Radiolaria
Müller 1858 emend.
Classes
Polycystinea
Acantharea
Sticholonchea
Radiolarians (also radiolaria) are amoeboid protozoa that produce intricate mineral skeletons, typically with a central capsule dividing the cell into
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Müller 1858 emend.
Classes
Polycystinea
Acantharea
Sticholonchea
Radiolarians (also radiolaria) are amoeboid protozoa that produce intricate mineral skeletons, typically with a central capsule dividing the cell into
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Foraminifera
d'Orbigny, 1826
Orders
Allogromiida
Carterinida
Fusulinida - extinct
Globigerinida
Involutinida - extinct
Lagenida
Miliolida
Robertinida
Rotaliida
Silicoloculinida
Spirillinida
Textulariida
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d'Orbigny, 1826
Orders
Allogromiida
Carterinida
Fusulinida - extinct
Globigerinida
Involutinida - extinct
Lagenida
Miliolida
Robertinida
Rotaliida
Silicoloculinida
Spirillinida
Textulariida
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SHARK
General
Vincent Rijmen, Joan Daemen, Bart Preneel, Antoon Bosselaers, Erik De Win
1996
KHAZAD, Rijndael
Cipher detail
Key size(s):| 128 bits
Block size(s):| 64 bits
Substitution-permutation network
6
In cryptography,
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General
Vincent Rijmen, Joan Daemen, Bart Preneel, Antoon Bosselaers, Erik De Win
1996
KHAZAD, Rijndael
Cipher detail
Key size(s):| 128 bits
Block size(s):| 64 bits
Substitution-permutation network
6
In cryptography,
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Basalt (IPA: /ˈbæsɒlt, bəˈsɒlt/) is a common gray to black extrusive volcanic rock. It is usually fine-grained due to rapid cooling of lava on the Earth's surface.
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1 centimetre =
SI units
010−3 m 0 mm
US customary / Imperial units
010−3 ft 0 in
A centimetre (American spelling: centimeter, symbol cmSI units
010−3 m 0 mm
US customary / Imperial units
010−3 ft 0 in
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Oceanic crust 0-20 Ma
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Precipitation is the formation of a solid in a solution during a chemical reaction. When the chemical reaction occurs the solid formed is called the precipitate. This can occur when an insoluble substance, the precipitate
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hot spring is a spring that is produced by the emergence of geothermally-heated groundwater from the earth's crust. There are hot springs all over the earth, on every continent and even under the oceans and seas.
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Volcano:
1. Large magma chamber
2. Bedrock
3. Conduit (pipe)
4. Base
5. Sill
6. Branch pipe
7. Layers of ash emitted by the volcano
8. Flank 9. Layers of lava emitted by the volcano
10. Throat
11. Parasitic cone
12. Lava flow
13. Vent
14.
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1. Large magma chamber
2. Bedrock
3. Conduit (pipe)
4. Base
5. Sill
6. Branch pipe
7. Layers of ash emitted by the volcano
8. Flank 9. Layers of lava emitted by the volcano
10. Throat
11. Parasitic cone
12. Lava flow
13. Vent
14.
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2, 3
(oxides: acidic, basic or amphoteric
depending on the oxidation state)
Electronegativity 1.55 (Pauling scale)
Ionization energies
(more) 1st: 717.3 kJmol−1
2nd: 1509.
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(oxides: acidic, basic or amphoteric
depending on the oxidation state)
Electronegativity 1.55 (Pauling scale)
Ionization energies
(more) 1st: 717.3 kJmol−1
2nd: 1509.
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2, 3
(mildly basic oxide)
Electronegativity 1.91 (Pauling scale)
Ionization energies
(more) 1st: 737.1 kJmol−1
2nd: 1753.0 kJmol−1
3rd: 3395 kJmol−1
Atomic radius 135 pm
Atomic radius (calc.
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(mildly basic oxide)
Electronegativity 1.91 (Pauling scale)
Ionization energies
(more) 1st: 737.1 kJmol−1
2nd: 1753.0 kJmol−1
3rd: 3395 kJmol−1
Atomic radius 135 pm
Atomic radius (calc.
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2, 1
(mildly basic oxide)
Electronegativity 1.90 (Pauling scale)
Ionization energies
(more) 1st: 745.5 kJmol−1
2nd: 1957.9 kJmol−1
3rd: 3666 kJmol−1
Atomic radius 135 pm
Atomic radius (calc.
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(mildly basic oxide)
Electronegativity 1.90 (Pauling scale)
Ionization energies
(more) 1st: 745.5 kJmol−1
2nd: 1957.9 kJmol−1
3rd: 3666 kJmol−1
Atomic radius 135 pm
Atomic radius (calc.
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2, 3
(amphoteric oxide)
Electronegativity 1.88 (Pauling scale)
Ionization energies
(more) 1st: 760.4 kJmol−1
2nd: 1648 kJmol−1
3rd: 3232 kJmol−1
Atomic radius 135 pm
Atomic radius (calc.
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(amphoteric oxide)
Electronegativity 1.88 (Pauling scale)
Ionization energies
(more) 1st: 760.4 kJmol−1
2nd: 1648 kJmol−1
3rd: 3232 kJmol−1
Atomic radius 135 pm
Atomic radius (calc.
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3, 4, 6
(amphoteric oxide)
Electronegativity 1.83 (Pauling scale)
Ionization energies
(more) 1st: 762.5 kJmol−1
2nd: 1561.9 kJmol−1
3rd: 2957 kJmol−1
Atomic radius 140 pm
Atomic radius (calc.
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(amphoteric oxide)
Electronegativity 1.83 (Pauling scale)
Ionization energies
(more) 1st: 762.5 kJmol−1
2nd: 1561.9 kJmol−1
3rd: 2957 kJmol−1
Atomic radius 140 pm
Atomic radius (calc.
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Silicon (IPA: /ˈsɪlɪkən/ or /ˈsɪlɪˌkɑn/, Latin: silicium
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Aluminium (IPA: /ˌæljʊˈmɪniəm/, /ˌæljəˈmɪniəm/) or aluminum (IPA: /əˈluːmɪnəm/
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Calcium (IPA: /ˈkalsiəm/) is the chemical element in the periodic table that has the symbol Ca and atomic number 20. It has an atomic mass of 40.078.
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Sodium (IPA: /ˈsəʊdiəm/) is a chemical element which has the symbol Na (Latin: natrium), atomic number 11, atomic mass 22.9898 g/mol, common oxidation number +1.
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Magnesium has the symbol Mg, the atomic number 12, and an atomic mass of 24.31. Magnesium is the ninth most abundant element in the universe by mass. It constitutes about 2% of the Earth's crust by mass, and it is the third most abundant element dissolved in seawater.
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Potassium (IPA: /pə(ʊ)ˈtasiəm/, /pə'tæsiəm/) is a chemical element. It has the symbol K (Arabic: al qalja
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Titanium (IPA: /tʌɪˈteɪniəm/) is a chemical element; in the periodic table it has the symbol Ti and atomic number 22.
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Barium (IPA: /ˈbɛːɹiəm/) is a chemical element. It has the symbol Ba, and atomic number 56. Barium is a soft silvery metallic alkaline earth metal.
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1, −1
(amphoteric oxide)
Electronegativity 2.20 (Pauling scale) More
Atomic radius 25 pm
Atomic radius (calc.) 53 pm
Covalent radius 37 pm
Van der Waals radius 120 pm
Miscellaneous
Thermal conductivity (300 K) 180.
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(amphoteric oxide)
Electronegativity 2.20 (Pauling scale) More
Atomic radius 25 pm
Atomic radius (calc.) 53 pm
Covalent radius 37 pm
Van der Waals radius 120 pm
Miscellaneous
Thermal conductivity (300 K) 180.
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2, −1
(neutral oxide)
Electronegativity 3.44 (Pauling scale)
Ionization energies
(more) 1st: 1313.9 kJmol−1
2nd: 3388.3 kJmol−1
3rd: 5300.5 kJmol−1
Atomic radius 60 pm
Atomic radius (calc.
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(neutral oxide)
Electronegativity 3.44 (Pauling scale)
Ionization energies
(more) 1st: 1313.9 kJmol−1
2nd: 3388.3 kJmol−1
3rd: 5300.5 kJmol−1
Atomic radius 60 pm
Atomic radius (calc.
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Herod_Archelaus