Chemistry:Magnetite

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Short description: Iron ore mineral
Magnetite
Magnetite-118736.jpg
Magnetite from Bolivia
General
Category
Formula
(repeating unit)		iron(II,III) oxide, Fe2+Fe3+
2O
4
Strunz classification4.BB.05
Crystal systemIsometric
Crystal classHexoctahedral (m3m)
H-M symbol: (4/m 3 2/m)
Space groupFd3m (no. 227)
Unit cella = 8.397 Å; Z = 8
Identification
ColorBlack, gray with brownish tint in reflected sun
Crystal habitOctahedral, fine granular to massive
TwinningOn {Ill} as both twin and composition plane, the spinel law, as contact twins
CleavageIndistinct, parting on {Ill}, very good
FractureUneven
TenacityBrittle
Mohs scale hardness5.5–6.5
|re|er}}Metallic
StreakBlack
DiaphaneityOpaque
Specific gravity5.17–5.18
SolubilityDissolves slowly in hydrochloric acid
References[1][2][3][4]
Major varieties
LodestoneMagnetic with definite north and south poles
Magnetite is one of the very few minerals that is ferrimagnetic; it is attracted by a magnet as shown here
Unit cell of magnetite. The gray spheres are oxygen, green are divalent iron, blue are trivalent iron. Also shown are an iron atom in an octahedral space (light blue) and another in a tetrahedral space (gray).

Magnetite is a mineral and one of the main iron ores, with the chemical formula Fe2+Fe3+
2O
4. It is one of the oxides of iron, and is ferrimagnetic;[6] it is attracted to a magnet and can be magnetized to become a permanent magnet itself.[7][8] With the exception of extremely rare native iron deposits, it is the most magnetic of all the naturally occurring minerals on Earth.[7][9] Naturally magnetized pieces of magnetite, called lodestone, will attract small pieces of iron, which is how ancient peoples first discovered the property of magnetism.[10]

Magnetite is black or brownish-black with a metallic luster, has a Mohs hardness of 5–6 and leaves a black streak.[7] Small grains of magnetite are very common in igneous and metamorphic rocks.[11]

The chemical IUPAC name is iron(II,III) oxide and the common chemical name is ferrous-ferric oxide.[12]

Properties

In addition to igneous rocks, magnetite also occurs in sedimentary rocks, including banded iron formations and in lake and marine sediments as both detrital grains and as magnetofossils. Magnetite nanoparticles are also thought to form in soils, where they probably oxidize rapidly to maghemite.[13]

Crystal structure

The chemical composition of magnetite is Fe2+(Fe3+)2(O2-)4. This indicates that magnetite contains both ferrous (divalent) and ferric (trivalent) iron, suggesting crystallization in an environment containing intermediate levels of oxygen.[14][15] The main details of its structure were established in 1915. It was one of the first crystal structures to be obtained using X-ray diffraction. The structure is inverse spinel, with O2- ions forming a face-centered cubic lattice and iron cations occupying interstitial sites. Half of the Fe3+ cations occupy tetrahedral sites while the other half, along with Fe2+ cations, occupy octahedral sites. The unit cell consists of thirty-two O2- ions and unit cell length is a = 0.839 nm.[15][16]

As a member of the inverse spinel group, magnetite can form solid solutions with similarly structured minerals, including ulvospinel (Fe
2TiO
4) and magnesioferrite (MgFe
2O
4).[17]

Titanomagnetite, also known as titaniferous magnetite, is a solid solution between magnetite and ulvospinel that crystallizes in many mafic igneous rocks. Titanomagnetite may undergo oxy-exsolution during cooling, resulting in ingrowths of magnetite and ilmenite.[17]

Crystal morphology and size

Natural and synthetic magnetite occurs most commonly as octahedral crystals bounded by {111} planes and as rhombic-dodecahedra.[15] Twinning occurs on the {111} plane.[2]

Hydrothermal synthesis usually produces single octahedral crystals which can be as large as 10 mm (0.39 in) across.[15] In the presence of mineralizers such as 0.1 M HI or 2 M NH4Cl and at 0.207 MPa at 416–800 °C, magnetite grew as crystals whose shapes were a combination of rhombic-dodechahedra forms.[15] The crystals were more rounded than usual. The appearance of higher forms was considered as a result from a decrease in the surface energies caused by the lower surface to volume ratio in the rounded crystals.[15]

Reactions

Magnetite has been important in understanding the conditions under which rocks form. Magnetite reacts with oxygen to produce hematite, and the mineral pair forms a buffer that can control how oxidizing its environment is (the oxygen fugacity). This buffer is known as the hematite-magnetite or HM buffer. At lower oxygen levels, magnetite can form a buffer with quartz and fayalite known as the QFM buffer. At still lower oxygen levels, magnetite forms a buffer with wüstite known as the MW buffer. The QFM and MW buffers have been used extensively in laboratory experiments on rock chemistry. The QFM buffer, in particular, produces an oxygen fugacity close to that of most igneous rocks.[18][19]

Commonly, igneous rocks contain solid solutions of both titanomagnetite and hemoilmenite or titanohematite. Compositions of the mineral pairs are used to calculate oxygen fugacity: a range of oxidizing conditions are found in magmas and the oxidation state helps to determine how the magmas might evolve by fractional crystallization.[20] Magnetite also is produced from peridotites and dunites by serpentinization.[21]

Magnetic properties

Lodestones were used as an early form of magnetic compass. Magnetite has been a critical tool in paleomagnetism, a science important in understanding plate tectonics and as historic data for magnetohydrodynamics and other scientific fields.[22]

The relationships between magnetite and other iron oxide minerals such as ilmenite, hematite, and ulvospinel have been much studied; the reactions between these minerals and oxygen influence how and when magnetite preserves a record of the Earth's magnetic field.[23]

At low temperatures, magnetite undergoes a crystal structure phase transition from a monoclinic structure to a cubic structure known as the Verwey transition. Optical studies show that this metal to insulator transition is sharp and occurs around 120 K.[24] The Verwey transition is dependent on grain size, domain state, pressure,[25] and the iron-oxygen stoichiometry.[26] An isotropic point also occurs near the Verwey transition around 130 K, at which point the sign of the magnetocrystalline anisotropy constant changes from positive to negative.[27] The Curie temperature of magnetite is 580 °C (853 K; 1,076 °F).[28]

If magnetite is in a large enough quantity it can be found in aeromagnetic surveys using a magnetometer which measures magnetic intensities.[29]

Melting point

Solid magnetite particles melt at about 1,583–1,597 °C (2,881–2,907 °F).[30][31](p794)

Distribution of deposits

Magnetite and other heavy minerals (dark) in a quartz beach sand (Chennai, India ).

Magnetite is sometimes found in large quantities in beach sand. Such black sands (mineral sands or iron sands) are found in various places, such as Lung Kwu Tan in Hong Kong; California , United States; and the west coast of the North Island of New Zealand.[32] The magnetite, eroded from rocks, is carried to the beach by rivers and concentrated by wave action and currents. Huge deposits have been found in banded iron formations.[33][34] These sedimentary rocks have been used to infer changes in the oxygen content of the atmosphere of the Earth.[35]

Large deposits of magnetite are also found in the Atacama region of Chile (Chilean Iron Belt);[36] the Valentines region of Uruguay;[37] Kiruna, Sweden;[38] the Tallawang region of New South Wales;[39] and in the Adirondack Mountains of New York in the United States.[40] Kediet ej Jill, the highest mountain of Mauritania, is made entirely of the mineral.[41] Deposits are also found in Norway , Romania, and Ukraine .[42] Magnetite-rich sand dunes are found in southern Peru.[43] In 2005, an exploration company, Cardero Resources, discovered a vast deposit of magnetite-bearing sand dunes in Peru. The dune field covers 250 square kilometers (100 sq mi), with the highest dune at over 2,000 meters (6,560 ft) above the desert floor. The sand contains 10% magnetite.[44]

In large enough quantities magnetite can affect compass navigation. In Tasmania there are many areas with highly magnetized rocks that can greatly influence compasses. Extra steps and repeated observations are required when using a compass in Tasmania to keep navigation problems to the minimum.[45]

Magnetite crystals with a cubic habit are rare but have been found at Balmat, St. Lawrence County, New York,[46][47] and at Långban, Sweden.[48] This habit may be a result of crystallization in the presence of cations such as zinc.[49]

Magnetite can also be found in fossils due to biomineralization and are referred to as magnetofossils.[50] There are also instances of magnetite with origins in space coming from meteorites.[51]

Biological occurrences

Biomagnetism is usually related to the presence of biogenic crystals of magnetite, which occur widely in organisms.[52] These organisms range from magnetotactic bacteria (e.g., Magnetospirillum magnetotacticum) to animals, including humans, where magnetite crystals (and other magnetically sensitive compounds) are found in different organs, depending on the species.[53][54] Biomagnetites account for the effects of weak magnetic fields on biological systems.[55] There is also a chemical basis for cellular sensitivity to electric and magnetic fields (galvanotaxis).[56]

Magnetite magnetosomes in Gammaproteobacteria

Pure magnetite particles are biomineralized in magnetosomes, which are produced by several species of magnetotactic bacteria. Magnetosomes consist of long chains of oriented magnetite particle that are used by bacteria for navigation. After the death of these bacteria, the magnetite particles in magnetosomes may be preserved in sediments as magnetofossils. Some types of anaerobic bacteria that are not magnetotactic can also create magnetite in oxygen free sediments by reducing amorphic ferric oxide to magnetite.[57]

Several species of birds are known to incorporate magnetite crystals in the upper beak for magnetoreception,[58] which (in conjunction with cryptochromes in the retina) gives them the ability to sense the direction, polarity, and magnitude of the ambient magnetic field.[53][59]

Chitons, a type of mollusk, have a tongue-like structure known as a radula, covered with magnetite-coated teeth, or denticles.[60] The hardness of the magnetite helps in breaking down food.

Biological magnetite may store information about the magnetic fields the organism was exposed to, potentially allowing scientists to learn about the migration of the organism or about changes in the Earth's magnetic field over time.[61]

Human brain

Living organisms can produce magnetite.[54] In humans, magnetite can be found in various parts of the brain including the frontal, parietal, occipital, and temporal lobes, brainstem, cerebellum and basal ganglia.[54][62] Iron can be found in three forms in the brain – magnetite, hemoglobin (blood) and ferritin (protein), and areas of the brain related to motor function generally contain more iron.[62][63] Magnetite can be found in the hippocampus. The hippocampus is associated with information processing, specifically learning and memory.[62] However, magnetite can have toxic effects due to its charge or magnetic nature and its involvement in oxidative stress or the production of free radicals.[64] Research suggests that beta-amyloid plaques and tau proteins associated with neurodegenerative disease frequently occur after oxidative stress and the build-up of iron.[62]

Some researchers also suggest that humans possess a magnetic sense,[65] proposing that this could allow certain people to use magnetoreception for navigation.[66] The role of magnetite in the brain is still not well understood, and there has been a general lag in applying more modern, interdisciplinary techniques to the study of biomagnetism.[67]

Electron microscope scans of human brain-tissue samples are able to differentiate between magnetite produced by the body's own cells and magnetite absorbed from airborne pollution, the natural forms being jagged and crystalline, while magnetite pollution occurs as rounded nanoparticles. Potentially a human health hazard, airborne magnetite is a result of pollution (specifically combustion). These nanoparticles can travel to the brain via the olfactory nerve, increasing the concentration of magnetite in the brain.[62][64] In some brain samples, the nanoparticle pollution outnumbers the natural particles by as much as 100:1, and such pollution-borne magnetite particles may be linked to abnormal neural deterioration. In one study, the characteristic nanoparticles were found in the brains of 37 people: 29 of these, aged 3 to 85, had lived and died in Mexico City, a significant air pollution hotspot. Some of the further eight, aged 62 to 92, from Manchester, England, had died with varying severities of neurodegenerative diseases.[68] Such particles could conceivably contribute to diseases like Alzheimer's disease.[69] Though a causal link has not yet been established, laboratory studies suggest that iron oxides such as magnetite are a component of protein plaques in the brain. Such plaques have been linked to Alzheimer's disease.[70]

Increased iron levels, specifically magnetic iron, have been found in portions of the brain in Alzheimer's patients.[71] Monitoring changes in iron concentrations may make it possible to detect the loss of neurons and the development of neurodegenerative diseases prior to the onset of symptoms[63][71] due to the relationship between magnetite and ferritin.[62] In tissue, magnetite and ferritin can produce small magnetic fields which will interact with magnetic resonance imaging (MRI) creating contrast.[71] Huntington patients have not shown increased magnetite levels; however, high levels have been found in study mice.[62]

Applications

Due to its high iron content, magnetite has long been a major iron ore.[72] It is reduced in blast furnaces to pig iron or sponge iron for conversion to steel.[73]

Magnetic recording

Audio recording using magnetic acetate tape was developed in the 1930s. The German magnetophon first utilized magnetite powder that BASF coated onto cellulose acetate before soon switching to gamma ferric oxide for its superior morphology.[74] Following World War II, 3M Company continued work on the German design. In 1946, the 3M researchers found they could also improve their own magnetite-based paper tape, which utilized powders of cubic crystals, by replacing the magnetite with needle-shaped particles of gamma ferric oxide (γ-Fe2O3).[74]

Catalysis

Approximately 2–3% of the world's energy budget is allocated to the Haber Process for nitrogen fixation, which relies on magnetite-derived catalysts. The industrial catalyst is obtained from finely ground iron powder, which is usually obtained by reduction of high-purity magnetite. The pulverized iron metal is burnt (oxidized) to give magnetite or wüstite of a defined particle size. The magnetite (or wüstite) particles are then partially reduced, removing some of the oxygen in the process. The resulting catalyst particles consist of a core of magnetite, encased in a shell of wüstite, which in turn is surrounded by an outer shell of iron metal. The catalyst maintains most of its bulk volume during the reduction, resulting in a highly porous high-surface-area material, which enhances its effectiveness as a catalyst.[75][76]

Magnetite nanoparticles

Magnetite micro- and nanoparticles are used in a variety of applications, from biomedical to environmental. One use is in water purification: in high gradient magnetic separation, magnetite nanoparticles introduced into contaminated water will bind to the suspended particles (solids, bacteria, or plankton, for example) and settle to the bottom of the fluid, allowing the contaminants to be removed and the magnetite particles to be recycled and reused.[77] This method works with radioactive and carcinogenic particles as well, making it an important cleanup tool in the case of heavy metals introduced into water systems.[78]

Another application of magnetic nanoparticles is in the creation of ferrofluids. These are used in several ways. Ferrofluids can be used for targeted drug delivery in the human body.[77] The magnetization of the particles bound with drug molecules allows "magnetic dragging" of the solution to the desired area of the body. This would allow the treatment of only a small area of the body, rather than the body as a whole, and could be highly useful in cancer treatment, among other things. Ferrofluids are also used in magnetic resonance imaging (MRI) technology.[79]

Coal mining industry

For the separation of coal from waste, dense medium baths were used. This technique employed the difference in densities between coal (1.3–1.4 tonnes per m3) and shales (2.2–2.4 tonnes per m3). In a medium with intermediate density (water with magnetite), stones sank and coal floated.[80]

Magnetene

Magnetene is a two-dimensional flat sheet of magnetite noted for its ultra-low-friction properties.[81]

Gallery

  • Octahedral crystals of magnetite up to 1.8 cm across, on cream colored feldspar crystals, locality: Cerro Huañaquino, Potosí Department, Bolivia

  • Magnetite crystals with epitaxial elevations on their faces

  • Magnetite in contrasting chalcopyrite matrix

  • Magnetite with a rare cubic habit from St. Lawrence County, New York

See also

References

  1. ↑ Anthony, John W.; Bideaux, Richard A.; Bladh, Kenneth W.. "Magnetite". Handbook of Mineralogy. Chantilly, VA: Mineralogical Society of America. pp. 333. http://www.handbookofmineralogy.org/pdfs/magnetite.pdf. Retrieved 15 November 2018. 
  2. ↑ 2.0 2.1 "Magnetite". mindat.org and the Hudson Institute of Mineralogy. http://www.mindat.org/min-2538.html. 
  3. ↑ Barthelmy, Dave. "Magnetite Mineral Data". webmineral.com. http://webmineral.com/data/Magnetite.shtml. 
  4. ↑ Hurlbut, Cornelius S.; Klein, Cornelis (1985). Manual of Mineralogy (20th ed.). Wiley. ISBN 978-0-471-80580-9. https://archive.org/details/manualofmineralo00klei. 
  5. ↑ Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine 85 (3): 291–320. doi:10.1180/mgm.2021.43. Bibcode: 2021MinM...85..291W. 
  6. ↑ Chen, J.; Duffy, T.S.; Dobrzhinetskaya, L.F. et al., eds (2005). "A gigahertz ultrasonic interferometer for the diamond anvil cell and high-pressure elasticity of some iron-oxide minerals". Advances in High-Pressure Technology for Geophysical Applications. Elsevier Science. pp. 25–48. doi:10.1016/B978-044451979-5.50004-1. ISBN 978-0-444-51979-5. 
  7. ↑ 7.0 7.1 7.2 Hurlbut, Cornelius Searle; W. Edwin Sharp; Edward Salisbury Dana (1998). Dana's minerals and how to study them. John Wiley and Sons. pp. 96. ISBN 978-0-471-15677-2. https://archive.org/details/danasmineralshow00hurl/page/96. 
  8. ↑ Wasilewski, Peter; Günther Kletetschka (1999). "Lodestone: Nature's only permanent magnet - What it is and how it gets charged". Geophysical Research Letters 26 (15): 2275–78. doi:10.1029/1999GL900496. Bibcode: 1999GeoRL..26.2275W. 
  9. ↑ Harrison, R. J.; Dunin-Borkowski, RE; Putnis, A (2002). "Direct imaging of nanoscale magnetic interactions in minerals". Proceedings of the National Academy of Sciences 99 (26): 16556–16561. doi:10.1073/pnas.262514499. PMID 12482930. Bibcode: 2002PNAS...9916556H. 
  10. ↑ Du Trémolet de Lacheisserie, Étienne; Damien Gignoux; Michel Schlenker (2005). Magnetism: Fundamentals. Springer. pp. 3–6. ISBN 0-387-22967-1. https://books.google.com/books?id=MgCExarQD08C&pg=PA3. 
  11. ↑ Nesse, William D. (2000). Introduction to mineralogy. New York: Oxford University Press. p. 361. ISBN 9780195106916. 
  12. ↑ Morel, Mauricio; Martínez, Francisco; Mosquera, Edgar (October 2013). "Synthesis and characterization of magnetite nanoparticles from mineral magnetite". Journal of Magnetism and Magnetic Materials 343: 76–81. doi:10.1016/j.jmmm.2013.04.075. Bibcode: 2013JMMM..343...76M. 
  13. ↑ Maher, B. A.; Taylor, R. M. (1988). "Formation of ultrafine-grained magnetite in soils". Nature 336 (6197): 368–370. doi:10.1038/336368a0. Bibcode: 1988Natur.336..368M. 
  14. ↑ Kesler, Stephen E.; Simon, Adam F. (2015). Mineral resources, economics and the environment (2nd ed.). Cambridge, United Kingdom: Cambridge University Press. ISBN 9781107074910. OCLC 907621860. 
  15. ↑ 15.0 15.1 15.2 15.3 15.4 15.5 Cornell; Schwertmann (1996). The Iron Oxides. New York: VCH. pp. 28–30. ISBN 978-3-527-28576-1. 
  16. ↑ an alternative visualisation of the crystal structure of Magnetite using JSMol is found here.
  17. ↑ 17.0 17.1 Nesse 2000, p. 360.
  18. ↑ Carmichael, Ian S.E.; Ghiorso, Mark S. (June 1986). "Oxidation-reduction relations in basic magma: a case for homogeneous equilibria". Earth and Planetary Science Letters 78 (2–3): 200–210. doi:10.1016/0012-821X(86)90061-0. Bibcode: 1986E&PSL..78..200C. 
  19. ↑ Philpotts, Anthony R.; Ague, Jay J. (2009). Principles of igneous and metamorphic petrology (2nd ed.). Cambridge, UK: Cambridge University Press. pp. 261–265. ISBN 9780521880060. 
  20. ↑ McBirney, Alexander R. (1984). Igneous petrology. San Francisco, Calif.: Freeman, Cooper. pp. 125–127. ISBN 0198578105. 
  21. ↑ Yardley, B. W. D. (1989). An introduction to metamorphic petrology. Harlow, Essex, England: Longman Scientific & Technical. p. 42. ISBN 0582300967. 
  22. ↑ Nesse 2000, p. 361.
  23. ↑ Tauxe, Lisa (2010). Essentials of paleomagnetism. Berkeley: University of California Press. ISBN 9780520260313. 
  24. ↑ Gasparov, L. V. (2000). "Infrared and Raman studies of the Verwey transition in magnetite". Physical Review B 62 (12): 7939. doi:10.1103/PhysRevB.62.7939. Bibcode: 2000PhRvB..62.7939G. 
  25. ↑ Gasparov, L. V. (2005). "Magnetite: Raman study of the high-pressure and low-temperature effects". Journal of Applied Physics 97 (10): 10A922. doi:10.1063/1.1854476. 10A922. Bibcode: 2005JAP....97jA922G. 
  26. ↑ Aragón, Ricardo (1985). "Influence of nonstoichiometry on the Verwey transition". Phys. Rev. B 31 (1): 430–436. doi:10.1103/PhysRevB.31.430. PMID 9935445. Bibcode: 1985PhRvB..31..430A. 
  27. ↑ Encyclopedia of geomagnetism and paleomagnetism. Springer Science & Business Media. 2007. 
  28. ↑ Fabian, K.; Shcherbakov, V. P.; McEnroe, S. A. (April 2013). "Measuring the Curie temperature". Geochemistry, Geophysics, Geosystems 14 (4): 947–961. doi:10.1029/2012GC004440. Bibcode: 2013GGG....14..947F. 
  29. ↑ "Magnetic Surveys". Australian Mines Atlas. 2014-05-15. http://www.australianminesatlas.gov.au/education/down_under/exploration/magsurv.html. 
  30. ↑ "Magnetite" (in en). https://www.acs.org/content/acs/en/molecule-of-the-week/archive/m/magnetite.html. 
  31. ↑ Perrin Walker; William H. Tarn (1991). CRC handbook of metal etchants. Boca Raton: CRC Press. ISBN 0-8493-3623-6. OCLC 326982496. https://www.worldcat.org/oclc/326982496. 
  32. ↑ Templeton, Fleur. "1. Iron – an abundant resource - Iron and steel". Te Ara Encyclopedia of New Zealand. http://www.teara.govt.nz/en/iron-and-steel/1. Retrieved 4 January 2013. 
  33. ↑ Rasmussen, Birger; Muhling, Janet R. (March 2018). "Making magnetite late again: Evidence for widespread magnetite growth by thermal decomposition of siderite in Hamersley banded iron formations". Precambrian Research 306: 64–93. doi:10.1016/j.precamres.2017.12.017. Bibcode: 2018PreR..306...64R. 
  34. ↑ Keyser, William; Ciobanu, Cristiana L.; Cook, Nigel J.; Wade, Benjamin P.; Kennedy, Allen; Kontonikas-Charos, Alkiviadis; Ehrig, Kathy; Feltus, Holly et al. (February 2020). "Episodic mafic magmatism in the Eyre Peninsula: Defining syn- and post-depositional BIF environments for iron deposits in the Middleback Ranges, South Australia". Precambrian Research 337: 105535. doi:10.1016/j.precamres.2019.105535. Bibcode: 2020PreR..33705535K. 
  35. ↑ Klein, C. (1 October 2005). "Some Precambrian banded iron-formations (BIFs) from around the world: Their age, geologic setting, mineralogy, metamorphism, geochemistry, and origins". American Mineralogist 90 (10): 1473–1499. doi:10.2138/am.2005.1871. Bibcode: 2005AmMin..90.1473K. 
  36. ↑ Ménard, J. -J. (June 1995). "Relationship between altered pyroxene diorite and the magnetite mineralization in the Chilean Iron Belt, with emphasis on the El Algarrobo iron deposits (Atacama region, Chile)". Mineralium Deposita 30 (3–4): 268–274. doi:10.1007/BF00196362. Bibcode: 1995MinDe..30..268M. 
  37. ↑ Wallace, Roberts M. (1976). "Geological reconnaissance of some Uruguayan iron and manganese deposits in 1962". U.S. Geological Survey Open File Report. Open-File Report 76-466. doi:10.3133/ofr76466. https://pubs.usgs.gov/of/1976/0466/report.pdf. Retrieved 15 February 2021. 
  38. ↑ Knipping, Jaayke L.; Bilenker, Laura D.; Simon, Adam C.; Reich, Martin; Barra, Fernando; Deditius, Artur P.; Lundstrom, Craig; Bindeman, Ilya et al. (July 2015). "Giant Kiruna-type deposits form by efficient flotation of magmatic magnetite suspensions". Geology 43 (7): 591–594. doi:10.1130/G36650.1. Bibcode: 2015Geo....43..591K. 
  39. ↑ Clark, David A. (September 2012). "Interpretation of the magnetic gradient tensor and normalized source strength applied to the Tallawang magnetite skarn deposit, New South Wales, Australia". SEG Technical Program Expanded Abstracts 2012: 1–5. doi:10.1190/segam2012-0700.1. 
  40. ↑ Valley, Peter M.; Hanchar, John M.; Whitehouse, Martin J. (April 2011). "New insights on the evolution of the Lyon Mountain Granite and associated Kiruna-type magnetite-apatite deposits, Adirondack Mountains, New York State". Geosphere 7 (2): 357–389. doi:10.1130/GES00624.1. Bibcode: 2011Geosp...7..357V. 
  41. ↑ European Space Agency, esa.int (access: August 2 2020)
  42. ↑ Hurlbut & Klein 1985, p. 388.
  43. ↑ Parker Gay, S (March 1999). "Observations regarding the movement of barchan sand dunes in the Nazca to Tanaca area of southern Peru". Geomorphology 27 (3–4): 279–293. doi:10.1016/S0169-555X(98)00084-1. Bibcode: 1999Geomo..27..279P. 
  44. ↑ Moriarty, Bob (5 July 2005). "Ferrous Nonsnotus". http://www.321gold.com/editorials/moriarty/moriarty070505.html. 
  45. ↑ Leaman, David. "Magnetic Rocks - Their Effect on Compass Use and Navigation in Tasmania". https://eprints.utas.edu.au/13644/1/1997_Leaman_Magnetic_rst.pdf. 
  46. ↑ Chamberlain, Steven C.; Robinson, George W.; Lupulescu, Marian; Morgan, Timothy C.; Johnson, John T.; deLorraine, William B. (May 2008). "Cubic and Tetrahexahedral Magnetite". Rocks & Minerals 83 (3): 224–239. doi:10.3200/RMIN.83.3.224-239. 
  47. ↑ "The mineral Magnetite". http://www.minerals.net/mineral/magnetite.aspx. 
  48. ↑ Boström, Kurt (15 December 1972). "Magnetite Crystals of Cubic Habit from Långban, Sweden". Geologiska Föreningen i Stockholm Förhandlingar 94 (4): 572–574. doi:10.1080/11035897209453690. 
  49. ↑ Clark, T.M.; Evans, B.J. (1997). "Influence of chemical composition on the crystalline morphologies of magnetite". IEEE Transactions on Magnetics 33 (5): 4257–4259. doi:10.1109/20.619728. Bibcode: 1997ITM....33.4257C. 
  50. ↑ Chang, S. B. R.; Kirschvink, J. L. (May 1989). "Magnetofossils, the Magnetization of Sediments, and the Evolution of Magnetite Biomineralization". Annual Review of Earth and Planetary Sciences 17 (1): 169–195. doi:10.1146/annurev.ea.17.050189.001125. Bibcode: 1989AREPS..17..169C. http://web.gps.caltech.edu/~jkirschvink/pdfs/AnnualReviews89.pdf. Retrieved 15 November 2018. 
  51. ↑ Barber, D. J.; Scott, E. R. D. (14 May 2002). "Origin of supposedly biogenic magnetite in the Martian meteorite Allan Hills 84001". Proceedings of the National Academy of Sciences 99 (10): 6556–6561. doi:10.1073/pnas.102045799. PMID 12011420. Bibcode: 2002PNAS...99.6556B. 
  52. ↑ Kirschvink, J L; Walker, M M; Diebel, C E (2001). "Magnetite-based magnetoreception.". Current Opinion in Neurobiology 11 (4): 462–7. doi:10.1016/s0959-4388(00)00235-x. PMID 11502393. 
  53. ↑ 53.0 53.1 Wiltschko, Roswitha; Wiltschko, Wolfgang (2014). "Sensing magnetic directions in birds: radical pair processes involving cryptochrome". Biosensors 4 (3): 221–42. doi:10.3390/bios4030221. PMID 25587420. "Birds can use the geomagnetic field for compass orientation. Behavioral experiments, mostly with migrating passerines, revealed three characteristics of the avian magnetic compass: (1) it works spontaneously only in a narrow functional window around the intensity of the ambient magnetic field, but can adapt to other intensities, (2) it is an "inclination compass", not based on the polarity of the magnetic field, but the axial course of the field lines, and (3) it requires short-wavelength light from UV to 565 nm Green.". 
  54. ↑ 54.0 54.1 54.2 Kirschvink, Joseph (1992). "Magnetite biomineralization in the human brain". Proceedings of the National Academy of Sciences of the USA 89 (16): 7683–7687. doi:10.1073/pnas.89.16.7683. PMID 1502184. Bibcode: 1992PNAS...89.7683K. "Using an ultrasensitive superconducting magnetometer in a clean-lab environment, we have detected the presence of ferromagnetic material in a variety of tissues from the human brain.". 
  55. ↑ Kirschvink, J L; Kobayashi-Kirschvink, A; Diaz-Ricci, J C; Kirschvink, S J (1992). "Magnetite in human tissues: a mechanism for the biological effects of weak ELF magnetic fields.". Bioelectromagnetics Suppl 1: 101–13. doi:10.1002/bem.2250130710. PMID 1285705. "A simple calculation shows that magnetosomes moving in response to earth-strength ELF fields are capable of opening trans-membrane ion channels, in a fashion similar to those predicted by ionic resonance models. Hence, the presence of trace levels of biogenic magnetite in virtually all human tissues examined suggests that similar biophysical processes may explain a variety of weak field ELF bioeffects.". 
  56. ↑ Nakajima, Ken-ichi; Zhu, Kan; Sun, Yao-Hui; Hegyi, Bence; Zeng, Qunli; Murphy, Christopher J; Small, J Victor; Chen-Izu, Ye et al. (2015). "KCNJ15/Kir4.2 couples with polyamines to sense weak extracellular electric fields in galvanotaxis". Nature Communications 6: 8532. doi:10.1038/ncomms9532. PMID 26449415. Bibcode: 2015NatCo...6.8532N. "Taken together these data suggest a previously unknown two-molecule sensing mechanism in which KCNJ15/Kir4.2 couples with polyamines in sensing weak electric fields.". 
  57. ↑ Lovley, Derek; Stolz, John; Nord, Gordon; Phillips, Elizabeth. "Anaerobic production of magnetite by a dissimilatory iron-reducing microorganism". US Geological Survey, Reston, Virginia 22092, USA Department of Biochemistry, University of Massachusetts, Amherst, Massachusetts 01003, USA. http://www.geobacter.org/publication-files/Nature_1987_Nov.pdf. 
  58. ↑ Kishkinev, D A; Chernetsov, N S (2014). "[Magnetoreception systems in birds: a review of current research]". Zhurnal Obshcheĭ Biologii 75 (2): 104–23. PMID 25490840. "There are good reasons to believe that this visual magnetoreceptor processes compass magnetic information which is necessary for migratory orientation.". 
  59. ↑ Wiltschko, Roswitha; Stapput, Katrin; Thalau, Peter; Wiltschko, Wolfgang (2010). "Directional orientation of birds by the magnetic field under different light conditions.". Journal of the Royal Society, Interface 7 (Suppl 2): S163–77. doi:10.1098/rsif.2009.0367.focus. PMID 19864263. "Compass orientation controlled by the inclination compass ...allows birds to locate courses of different origin". 
  60. ↑ Lowenstam, H.A. (1967). "Lepidocrocite, an apatite mineral, and magnetic in teeth of chitons (Polyplacophora)". Science 156 (3780): 1373–1375. doi:10.1126/science.156.3780.1373. PMID 5610118. Bibcode: 1967Sci...156.1373L. "X-ray diffraction patterns show that the mature denticles of three extant chiton species are composed of the mineral lepidocrocite and an apatite mineral, probably francolite, in addition to magnetite.". 
  61. ↑ Bókkon, Istvan; Salari, Vahid (2010). "Information storing by biomagnetites". Journal of Biological Physics 36 (1): 109–20. doi:10.1007/s10867-009-9173-9. PMID 19728122. Bibcode: 2010arXiv1012.3368B. 
  62. ↑ 62.0 62.1 62.2 62.3 62.4 62.5 62.6 Magnetite Nano-Particles in Information Processing: From the Bacteria to the Human Brain Neocortex - ISBN:9781-61761-839-0
  63. ↑ 63.0 63.1 Zecca, Luigi; Youdim, Moussa B. H.; Riederer, Peter; Connor, James R.; Crichton, Robert R. (2004). "Iron, brain ageing and neurodegenerative disorders". Nature Reviews Neuroscience 5 (11): 863–873. doi:10.1038/nrn1537. PMID 15496864. 
  64. ↑ 64.0 64.1 Barbara A. Maher; Imad A. M. Ahmed; Vassil Karloukovski; Donald A. MacLaren; Penelope G. Foulds; David Allsop; David M. A. Mann; Ricardo Torres-Jardón et al. (2016). "Magnetite pollution nanoparticles in the human brain". PNAS 113 (39): 10797–10801. doi:10.1073/pnas.1605941113. PMID 27601646. Bibcode: 2016PNAS..11310797M. 
  65. ↑ Eric Hand (June 23, 2016). "Maverick scientist thinks he has discovered a magnetic sixth sense in humans". Science. doi:10.1126/science.aaf5803. https://www.science.org/content/article/maverick-scientist-thinks-he-has-discovered-magnetic-sixth-sense-humans-rev2. 
  66. ↑ Baker, R R (1988). "Human magnetoreception for navigation". Progress in Clinical and Biological Research 257: 63–80. PMID 3344279. 
  67. ↑ Kirschvink, Joseph L; Winklhofer, Michael; Walker, Michael M (2010). "Biophysics of magnetic orientation: strengthening the interface between theory and experimental design.". Journal of the Royal Society, Interface 7 (Suppl 2): S179–91. doi:10.1098/rsif.2009.0491.focus. PMID 20071390. 
  68. ↑ "Pollution particles 'get into brain'". BBC News. September 5, 2016. https://www.bbc.com/news/science-environment-37276219. 
  69. ↑ Maher, B.A.; Ahmed, I.A.; Karloukovski, V.; MacLaren, D.A.; Foulds, P.G.; Allsop, D.; Mann, D.M.; Torres-Jardón, R. et al. (2016). "Magnetite pollution nanoparticles in the human brain". Proceedings of the National Academy of Sciences 113 (39): 10797–10801. doi:10.1073/pnas.1605941113. PMID 27601646. Bibcode: 2016PNAS..11310797M. 
  70. ↑ Wilson, Clare (5 September 2016). "Air pollution is sending tiny magnetic particles into your brain". New Scientist 231 (3090). https://www.newscientist.com/article/2104654-air-pollution-is-sending-tiny-magnetic-particles-into-your-brain/. Retrieved 6 September 2016. 
  71. ↑ 71.0 71.1 71.2 Qin, Yuanyuan; Zhu, Wenzhen; Zhan, Chuanjia; Zhao, Lingyun; Wang, Jianzhi; Tian, Qing; Wang, Wei (August 2011). "Investigation on positive correlation of increased brain iron deposition with cognitive impairment in Alzheimer disease by using quantitative MR R2′ mapping". Journal of Huazhong University of Science and Technology [Medical Sciences] 31 (4): 578–585. doi:10.1007/s11596-011-0493-1. PMID 21823025. 
  72. ↑ Franz Oeters et al"Iron" in Ullmann's Encyclopedia of Industrial Chemistry, 2006, Wiley-VCH, Weinheim. doi:10.1002/14356007.a14_461.pub2
  73. ↑ Davis, E.W. (2004). Pioneering with taconite. Minnesota Historical Society Press. ISBN 0873510232. 
  74. ↑ 74.0 74.1 Schoenherr, Steven (2002). "The History of Magnetic Recording". Audio Engineering Society. http://www.aes.org/aeshc/docs/recording.technology.history/magnetic4.html. 
  75. ↑ Jozwiak, W. K.Expression error: Unrecognized word "etal". (2007). "Reduction behavior of iron oxides in hydrogen and carbon monoxide atmospheres". Applied Catalysis A: General 326: 17–27. doi:10.1016/j.apcata.2007.03.021. 
  76. ↑ Appl, Max (2006). "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a02_143.pub2. 
  77. ↑ 77.0 77.1 Blaney, Lee (2007). "Magnetite (Fe3O4): Properties, Synthesis, and Applications" (in en). The Lehigh Review 15 (5). https://preserve.lehigh.edu/cas-lehighreview-vol-15/5/. Retrieved 2017-12-15. 
  78. ↑ Rajput, Shalini; Pittman, Charles U.; Mohan, Dinesh (2016). "Magnetic magnetite (Fe 3 O 4 ) nanoparticle synthesis and applications for lead (Pb 2+ ) and chromium (Cr 6+ ) removal from water" (in en). Journal of Colloid and Interface Science 468: 334–346. doi:10.1016/j.jcis.2015.12.008. PMID 26859095. Bibcode: 2016JCIS..468..334R. 
  79. ↑ Stephen, Zachary R.; Kievit, Forrest M.; Zhang, Miqin (2011). "Magnetite nanoparticles for medical MR imaging" (in en). Materials Today 14 (7–8): 330–338. doi:10.1016/s1369-7021(11)70163-8. PMID 22389583. 
  80. ↑ Nyssen, J; Diependaele, S; Goossens, R (2012). "Belgium's burning coal tips - coupling thermographic ASTER imagery with topography to map debris slide susceptibility". Zeitschrift für Geomorphologie 56 (1): 23–52. doi:10.1127/0372-8854/2011/0061. Bibcode: 2012ZGm....56...23N. 
  81. ↑ Toronto, University of. "Magnetene: Graphene-like 2D material leverages quantum effects to achieve ultra-low friction". https://phys.org/news/2021-11-magnetene-graphene-like-2d-material-leverages.html. 

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