Rare earth element

Published: 14th July 2010
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Discovery and early history

Rare earth elements became known to the world with the discovery of the black mineral ytterbite (also known as gadolinite) by Lieutenant Carl Axel Arrhenius in the year 1787, in a quarry in the village of Ytterby, Sweden. Many of the rare earths are named for the scientists who discovered or elucidated the elemental properties, or for their geographical discovery, or for Latin or Greek references, or for mythical references:





Selected Usages




from the Greek "lanthanon," meaning I am hidden.

High refractive index glass, flint, hydrogen storage, battery-electrode, camera lens




for the Roman deity of fertility Ceres.

chemical oxidising agent, polishing powder, yellow colors in glass and ceramics, catalyst for Self-cleaning oven etc.




from the Greek "praso," meaning leek-green, and "didymos," meaning twin.

Rare-earth magnets, laser, green colors in glass and ceramics, flint




from the Greek "neo," meaning new-one, and "didymos," meaning twin.

Rare-earth magnets, laser, violet colors in glass and ceramics, ceramic capacitor




for the Titan Prometheus, who brought fire to mortals.

Nuclear battery




for Vasili Samarsky-Bykhovets, who discovered the rare earth ore samarskite.

Rare-earth magnets, Laser, neutron capture, maser




for the continent of Europe.

Red and blue phosphors, laser, mercury-vapor lamp




for Johan Gadolin (1760-1852), to honor his investigation of rare earths.

Rare-earth magnets, high refractive index glass or garnets, laser, x-ray tube, computer memory, neutron capture




for the village of Ytterby, Sweden, where the first rare earth ore was discovered.

Green phosphors, laser, fluorescent lamp




from the Greek "dysprositos," meaning hard to get.

Rare-earth magnets, laser,




for Stockholm (in Latin, "Holmia"), native city of one of its discoverers.





for the village of Ytterby, Sweden.

Laser, vanadium steel




for the mythological land of Thule.




for the village of Ytterby, Sweden.

Infrared Laser, chemical reducing agent




for Lutetia, the city which later became Paris.

The ytterbite, renamed to gadolinite in 1800, of Lt. Arrhenius reached Johann Gadolin, a University of Turku professor, and his analysis yielded an unknown oxide (earth) which he called Ytteria. Anders Gustav Ekeberg isolated beryllium from the gadolinite but failed to recognize other elements which the ore contained. After this discovery in 1794 a mineral from Bastns near Riddarhyttan, Sweden, which was believed to be an iron-tungsten mineral, was re-examined by Jns Jacob Berzelius and Wilhelm Hisinger. In 1803 they obtained a white oxide and called it ceria. Martin Heinrich Klaproth independently discovered the same oxide and called it ochroia.

Thus by 1803 there were two known rare earth elements, yttrium and cerium, although it took another 30 years for researchers to determine that other elements were contained in the two ores ceria and ytteria (the similarity of the rare earth metals' chemical properties made their separation difficult).

In 1839 Carl Gustav Mosander, an assistant of Berzelius, separated ceria by heating the nitrate and dissolving the product in nitric acid. He called the oxide of the soluble salt lanthana. It took him three more years to separate the lanthana further into didymia and pure lanthana. Didymia, although not further separable by Mosander's techniques was a mixture of oxides.

In 1842 Mosander also separated the ytteria into three oxides: pure ytteria, terbia and erbia (all the names are derived from the town name "Ytterby"). The earth giving pink salts he called terbium; the one which yielded yellow peroxide he called erbium.

So in 1842 the number of rare earth elements had reached six: yttrium, cerium, lanthanum, didymium, erbium and terbium.

Nils Johan Berlin and Marc Delafontaine tried also to separate the crude ytteria and found the same substances that Mosander obtained, but Berlin named (1860) the substance giving pink salts erbium and Delafontaine named the substance with the yellow peroxide terbium. This confusion led to several false claims of new elements, such as the mosandrium of J. Lawrence Smith, or the philippium and decipium of Delafontaine.

There were no further discoveries for 30 years, and the element didymium was listed in the periodic table of elements with a molecular mass of 138. In 1879 Delafontaine used the new technique of optical flame spectroscopy and found new spectral lines in didymia, and also in 1879 the new element samarium was isolated by Paul mile Lecoq de Boisbaudran from the mineral samarskite.

The samaria earth was further separated by Lecoq de Boisbaudran in 1886 and a similar result was obtained by Jean-Charles Galissard de Marignac by direct isolation from samarskithe. They named the element gadolinium after Johan Gadolin, and the oxide was gadolinia.

Further spectroscopic analysis between 1886 and 1901 of samaria, ytteria and samarskite by William Crookes, Lecoq de Boisbaudran and Eugne-Anatole Demaray yielded new spectroscopic lines indicating an unknown element. Fractional crystallization yielded europium in 1901.

In 1839 the third source for rare earths became available, a mineral similar to gadolinite, uranotantalum (now samarskite). This mineral from Miass in the southern Ural Mountains was described by Gustave Rose. The Russian chemist R. Harmann postulated the new element ilmenium must be present in the mineral, but later Christian Wilhelm Blomstrand, Jean Charles Galissard de Marignac, and Heinrich Rose only found tantalum and niobium.

The exact number of rare earth elements was unclear and a maximum number of 25 was estimated. The use of x-ray spectra (obtained by diffraction in crystals) of Henry Moseley made it possible to determine the atomic numbers. The absolute number of lanthanides had to be 15, with a still missing element 61.

Using this technique Moseley proved that hafnium was not a rare earth element and that the claims of Georges Urbain of having discovered element 72 were false.

The principal sources of rare earth elements are the minerals bastnsite, monazite, and loparite and the lateritic ion-adsorption clays. Despite their high relative abundance, rare earth minerals are more difficult to mine and extract than equivalent sources of transition metals (due in part to their similar chemical properties), making the rare earth elements relatively expensive. Their industrial use was very limited until efficient separation techniques were developed, such as ion exchange, fractional crystallization and liquid-liquid extraction during the late 1950s and early 1960s.


The following abbreviations are often used:

RE = rare earth

REM = rare earth metals

REE = rare earth elements

REO = rare earth oxides

LREE = light rare earth elements (La-Sm)

HREE = heavy rare earth elements (Eu-Lu)

Technological applications

These rare-earth oxides are used as tracers to determine which parts of a watershed are eroding. Clockwise from top center: praseodymium, cerium, lanthanum, neodymium, samarium, and gadolinium.

Rare earth elements are incorporated into many modern technological devices, including superconductors, samarium-cobalt and neodymium-iron-boron high-flux rare-earth magnets, electronic polishers, refining catalysts and hybrid car components (primarily batteries and magnets). Rare earth ions are used as the active ions in luminescent materials used in optoelectronics applications, most notably the Nd:YAG laser. Erbium-doped fiber amplifiers are significant devices in optical-fiber communication systems. Phosphors with rare earth dopants are also widely used in cathode ray tube technology such as television sets. The earliest color television CRTs had a poor-quality red; europium as a phosphor dopant made good red phosphors possible. Yttrium iron garnet (YIG) spheres have been useful as tunable microwave resonators. Rare earth oxides are mixed with tungsten to improve its high temperature properties for welding, replacing thorium, which was mildly hazardous to work with.

Global rare earth production

Global production 1950-2000

Until 1948, most of the world's rare earths were sourced from placer sand deposits in India and Brazil. Through the 1950s, South Africa took the status as the world's rare earth source, after large rare earth bearing veins were discovered in Monazite. Today, those Indian and South African deposits still produce some rare earth concentrates, but they are dwarfed by the scale of Chinese production. China now produces over 95% of the world's rare earth supply.

The use of rare earth elements in modern technology has increased dramatically over the past years. For example, dysprosium has gained significant importance for its use in the construction of hybrid car motors. Unfortunately, this new demand has strained supply, and there is growing concern that the world may soon face a shortage of the materials. In several years, worldwide demand for rare earth elements is expected to exceed supply by 40,000 tonnes annually unless major new sources are developed. All of the world's heavy rare earths (such as dysprosium) are sourced from Chinese rare earth sources such as the polymetallic Bayan Obo deposit. Illegal rare earth mines are common in rural China and are often known to release toxic wastes into the general water supply. A rare earth element mine in California is set to reopen by 2012. A site at Thor Lake in the Northwest Territories is also under development. Locations in Vietnam have also been considered.

Chinese export quotas have also resulted in a dramatic shift in the world's rare earth knowledge base. For example, the division of General Motors which deals with miniaturized magnet research shut down its US office and moved all of its staff to China in 2006.

On Sept. 1, 2009, China announced plans to reduce its quota to 35,000 tons per year in 2010-2015, supposedly to conserve scarce resources and protect the environment. Other sources of rare earth have been searched to avoid shortages and China's monopoly, mainly in South Africa, Brazil and the United States.

Geologic distribution

Due to lanthanide contraction, yttrium, which is trivalent, is of similar ionic size to dysprosium and its lanthanide neighbors. Due to the relatively gradual decrease in ionic size with increasing atomic number, the rare earth elements have always been difficult to separate. Even with eons of geological time, geochemical separation of the lanthanides has only rarely progressed much farther than a broad separation between light versus heavy lanthanides, otherwise known as the cerium and yttrium earths. This geochemical divide is reflected in the first two rare earths that were discovered, yttria in 1794 and ceria in 1803. As originally found, each comprised the entire mixture of the associated earths. Rare earth minerals, as found, usually are dominated by one group or the other, depending upon which size-range best fits the structural lattice. Thus, among the anhydrous rare earth phosphates, it is the tetragonal mineral xenotime that incorporates yttrium and the yttrium earths, whereas the monoclinic monazite phase incorporates cerium and the cerium earths preferentially. The smaller size of the yttrium group allows it a greater solid solubility in the rock-forming minerals that comprise the earth's mantle, and thus yttrium and the yttrium earths show less enrichment in the earth's crust, relative to chondritic abundance, than does cerium and the cerium earths. This has economic consequences: large orebodies of the cerium earths are known around the world, and are being actively exploited. Corresponding orebodies for yttrium tend to be rarer, smaller, and less concentrated. Most of the current supply of yttrium originates in the "ion adsorption clay" ores of Southern China. Some versions of these provide concentrates containing about 65% yttrium oxide, with the heavy lanthanides being present in ratios reflecting the Oddo-Harkins rule: even-numbered heavy lanthanides at abundances of about 5% each, and odd-numbered lanthanides at abundances of about 1% each. Similar compositions are found in xenotime or gadolinite.

Well-known minerals that contain yttrium include gadolinite, xenotime, samarskite, euxenite, fergusonite, yttrotantalite, yttrotungstite, yttrofluorite (a variety of fluorite), thalenite, yttrialite. Small amounts occur in zircon, which derives its typical yellow fluorescence from some of the accompanying heavy lanthanides. The zirconium mineral eudialyte, such as is found in southern Greenland, also contains small but potentially useful amounts of yttrium. Of the above yttrium minerals, most played a part in providing research quantities of lanthanides during the discovery days. Xenotime is occasionally recovered as a byproduct of heavy sand processing, but has never been nearly as abundant as the similarly recovered monazite (which typically contains a few percent of yttrium). Uranium ores processed in Ontario have occasionally yielded yttrium as a byproduct.

Well-known minerals that contain cerium and the light lanthanides include bastnaesite, monazite, allanite, loparite, ancylite, parisite, lanthanite, chevkinite, cerite, stillwellite, britholite, fluocerite, and cerianite. Over the years, monazite (marine sands from Brazil, India, or Australia; rock from South Africa), bastnaesite (from Mountain Pass California, or several localities in China), and loparite (Kola Peninsula, Russia) have been the principal ores of cerium and the light lanthanides.

A few sites are under development outside of China, the most significant of which are the Nolans Project in Central Australia, the remote Hoidas Lake project in northern Canada and the Mt. Weld project in Australia. The Hoidas Lake project has the potential to supply about 10% of the $1 billion of REE consumption that occurs in North America every year.

See also



^ Edited by N G Connelly and T Damhus (with R M Hartshorn and A T Hutton), ed (2005). Nomenclature of Inorganic Chemistry: IUPAC Recommendations 2005. Cambridge: RSC Publ.. ISBN 0-85404-438-8. http://www.iupac.org/publications/books/rbook/Red_Book_2005.pdf. Retrieved 2007-12-17. 

^ Gschneidner KA, Cappellen, ed (1987). "1787-1987 Two hundred Years of Rare Earths". Rare Earth Information Center, IPRT, North-Holland IS-RIC 10. 

^ Spedding F, Daane AH: "The Rare Earths", John Wiley & Sons, Inc., 1961

^ "News and events". US Department of Agriculture. http://www.ars.usda.gov/is/graphics/photos/jun05/d115-1.htm. Retrieved 2009-06-06. 

^ a b "Haxel G, Hedrick J, Orris J. 2006. Rare earth elements critical resources for high technology. Reston (VA): United States Geological Survey. USGS Fact Sheet: 08702.". http://pubs.usgs.gov/fs/2002/fs087-02/fs087-02.pdf. Retrieved 2008-04-19. 

^ a b ER, Rose. Rare Earths of the Grenville Subrovince Ontatio and Quebec. GSC Report Number 5910. Ottawa: Geological Survey of Canada Department of Mines and Technical Surveys, 1960.

^ G, Nishiyama. "Japan urges China to ease rare metals supply." 8 November 2007. Reuters Latest News. 10 March 2008 http://www.reuters.com/article/latestCrisis/idUSL08815827

^ "Cox C. 2008. Rare earth innovation. Herndon (VA): The Anchor House Inc;". http://theanchorhouse.com. Retrieved 2008-04-19. 

^ a b http://www.reuters.com/article/newsOne/idUSTRE57U02B20090831 As hybrid cars gobble rare metals, shortage looms, Aug 31, 2009

^ Chao ECT, Back JM, Minkin J, Tatsumoto M, Junwen W, Conrad JE, McKee EH, Zonglin H, Qingrun M. "Sedimentary carbonateosted giant Bayan Obo REEeb ore deposit of Inner Mongolia, China; a cornerstone example for giant polymetallic ore deposits of hydrothermal origin." 1997. United States Geological Survey Publications Warehouse. 29 February 2008 http://pubs.usgs.gov/bul/b2143/

^ Y, Lee. "South China Villagers Slam Pollution From Rare Earth Mine." 22 February 2008. RFA English Website. 16 March 2008 http://www.rfa.org/english/news/china_pollution-20080222.html

^ C, Cox. "Rare earth innovation: the silent shift to China." 16 November 2006. The Anchor House: Research on Rare Earth Elements. 29 February 2008 http://theanchorhouse.com/2006/11/

^ China To Limit Rare Earths Exports 1 September 2009 http://www.manufacturing.net/article.aspx?id=215574/

^ "Canadian Firms Step Up Search for Rare-Earth Metals". NYTimes.com. Reuters. 2009-09-09. http://www.nytimes.com/2009/09/10/business/global/10mineral.html?scp=10&sq=brazil&st=nyt. Retrieved 2009-09-15. 

^ "Lunn J. 2006. Great western minerals. London: Insigner Beaufort Equity Research". http://www.gwmg.ca/pdf/Insinger_Report.pdf. Retrieved 2008-04-19. 

^ "Hoidas Lake Project". http://www.gwmg.ca/projects/hoidas-lake. Retrieved 2008-09-24. 

External links

Rare Earth Metals Not So Rare But Valuable Retrieved 2009-09-10

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